Analysis of salmon and steelhead supplementation

[From the U.S. Government Printing Office, www.gpo.gov]

Analysis of Salmon and Steelhead
Supplementation
Part 1. Emphasis on Unpublished Reports and Present Programs
Part 2. Synthesis of Published Literature
Part 3 - Concepts for a Model to Evaluate Supplementation

Technical
Report
1990

U.S. Department of Energy
Bonneville Power Administration
Division of Fish & Wildlife

U.S. Department of Interior
U.S. Fish and Wildlife Service
Dworshak Fisheries Assistance
Office

September 1990

This report was funded by the Bonneville Power Administration (BPA),
U.S. Department of Energy, as part of BPA's program to protect, mitigate,
and enhance fish and wildlife affected by the development and operation
of hydroelectric facilities on the Columbia River and its tributaries. The
views in this report are the author's and do not necessarily represent the
views of BPA.

For copies of this report, write to:

Bonneville Power Administration
Division of Fish and Wildlife - PJ
P.O. Box 3621
Portland, OR 97208

ANALYSIS OF SALMON AND STEELHEAD SUPPLEMENTATION

PART 1: Emphasis on Unpublished Reports and Present Programs

PART 2: Synthesis of Published Literature

PART 3: Concepts for a Model to Evaluate Supplementation

Prepared by:
William H. Miller

Dworshak Fisheries Assistance Office
U.S. Fish and Wildlife Service

Prepared for

Thomas Vogel, Project Leader

Funded by

U.S. Department ofEnergy
Bonneville Power Administration
Division of Fish and Wildlife
Portland, Oregon 97208

Cotract No. DE-A179-88BP92663
Project No. 88-100

September 1990

TABLE OF CONTENTS

PART I ................ Emphasis on Unpublished Reports and Present Programs

PART II ............... Synthesis on Published Literature

PART III .............. Concepts of a Model to Evaluate Supplementation

ANALYSIS OF SALMON AND STEELHEAD
SUPPLEMENTATION: EMPHASIS ON
UNPUBLISHED REPORTS AND PRESENT PROGRAMS

PART 1

Prepared by:
William H. Miller
Travis C. Coley
Howard L. Burge
Tom T. Kisanuki

Dworshak Fisheries Assistance Office
U.S. Fish and Wildlife Service
Ahsahka,ldaho

Submitted to:
U.S. Department of Energy
Bonneville Power Administration

Project No. 88-100

September 1990

CONTENTS

PAGE

Preface ............................................. i

Acknowledgements .......... .......................... ii

Abstract ............................................. iii

Introduction .......................................... 1

Methods ............................................ 2

Study Area ........................................... 2

General Overview ..................................... 2

Results ............................................. 3
General ........................................... 3
Oregon ............................................ 4
Washington ......................................... 8
Idaho .............................................. 12
California .......................................... 16
Alaska ............................................. 21
British Columbia ..................................... 26
New England Atlantic Salmon Program ................... 31

Conclusions ......................................... 36

Recommendations ..................................... 41
Recommended Research ............................... 41

Literature Cited ....................................... 43

Appendix A - Database for unpublished and ongoing supplementation projects"
reviewed for "Analysis of Salmon and Steelhead Supplementation:
Emphasis on Unpublished Reports and Present Programs."

PREFACE

This report was part of a Bonneville Power Administration (BPA) funded project to
summarize information on supplementation of salmon and steelhead, Project No. 88-100.
BPA project officer for this contract was Tom Vogel. Primary geographic area of
concern was the Northwestern U.S. with special emphasis on the Columbia River Basin.

There were three reports prepared under this BPA project:

1. Analysis of Salmon and Steelhead Supplementation: Emphasi on Unpublished
Report and Present Program by W.H. Miller, T.C. Coley, H.L. Burge and T.T.
Kisanuki.

2. Supplementation of Salmon and Steelhead Stocks With Hatche Fish: A
Synthesi of Published Literature by C.R. Steward and T.C. Bjornn.

3. Concepts for a Model to Evaluate Supplementation of Natural Salmon and
Steelhead Stocks With Hatche Fish by T.C. Bjornn and C.R. Steward.

The two reports by Steward and Bjornn were contracted studies with the Idaho
Cooperative Fish and Wildlife Research Unit at the University of Idaho in Moscow,
Idaho. The overall objectives of the BPA funded project were: (1) summarize and
evaluate past and current supplementation of salmon and steelhead; (2) develop a
conceptual "model" of processes affecting the results of supplementation; and (3) make
recommendations regarding future supplementation research.

ACKNOWLEDGEMENTS

We thank the many Oregon, Washington, Idaho, California, Alaska, British Columbia,
and New England fishery biologists for their contribution of time and knowledge. Tom
Macy, Karen Smith, Phil Wampler, and Jon Anderson of the Fish and Wildlife Service's
(FWS) Vancouver and Olympia Fisheries Assistance Offices assisted in data collection.
Diane Praest, FWS Dworshak Fisheries Assistance Office, typed many drafts and the
final manuscript.

ABSTRACT

Supplementation or planting salmon and steelhead into various locations in the
Columbia River drainage has occurred for over 100 years. All life stages, from eggs to
adults, have been used by fishery managers in attempts to establish, rebuild, or maintain
anadromous runs. This report summarizes and evaluates results of past and current
supplementation of salmon and steelhead. Conclusions and recommendations are made
concerning supplementation.

Hatchery rearing conditions and stocking methods can affect post release survival of
hatchery fish. Stress was considered by many biologists to be a key factor, in survival of
stocked anadromous fish. Smolts were the most common life stage released and size of
smolts correlated positively with survival. Success of hatchery stockings of eggs and pre-
smolts was found to be better if they are put into productive, underseeded habitats.
Stocking time, method, species stocked, and environmental conditions of the receiving
waters, including other fish species present, are factors to consider in supplementation
programs.

The unpublished supplementation literature was reviewed primarily by the authors of this
report. Direct contact was made in person or by telephone and data compiled on a
computer database. Areas covered included Oregon, Washington, Idaho, Alaska,
California, British Columbia, and the New England states working with Atlantic salmon.
Over 300 projects were reviewed and entered into a computer database. The database
information is contained in Appendix A of this report.

Our conclusions based on the published literature and the unpublished projects reviewed
are as follows:

-Examples of success at rebuilding self-sustaining anadromous fish runs with hatchery
fish are scarce. We reviewed 316 projects in the unpublished and ongoing work.
Only 25 were successful for supplementing natural existing runs, although many were
successful at returning adult fish.
-Successes from outplanting hatchery fish were primarily in harvest augmentation, a
term we use to -describe stocking where the primary purpose is to return adults for
sport, tribal or commercial harvest.
-Adverse impacts to wild stocks have been shown or postulated for about every type of
hatchery fish introduction where the intent was to rebuild runs.
-Reestablishing runs or introductions to areas not inhabited by wild/natural populations
have shown g6od successes.
-Tlie stock of fish is an important factor to consider when supplementing. The closer
the hatchery stock is genetically to the natural stock, the higher the chances for
success.

iii

-Chinook are one of the most difficult salmon species to supplement. A return rate,
smolt or pre-smolt-to-adult, of 3-5 percent is considered good by most managers for
this species.
-Salmon species with the shortest freshwater life cycle, e.g., chum and pink, have shown
higher success from supplementation, than longer freshwater cycle salmon.
-Short-run stocks of salmon and steelhead have responded more positively to
supplementation than longer-run stocks.
-Wild/natural fish have consistently shown a much higher smolt-to-adult survival rate
than hatchery fish.
-Overstocking of hatchery fish may be a significant problem in many supplementation
projects.
-The use of wild broodstock by British Columbia has shown success in their chinook and
steelhead supplementation programs.
-Both Alaska and British Columbia are having some success using streamside incubation
boxes and subsequent outplanting of fry.

Overall, we concluded that protection and nurturing of wild/natural runs needs to be a
top management priority. There are no guarantees that hatchery supplementation can
replace or consistently augment natural production. For the Columbia River system, we
concluded that all hatchery fish should be marked for visual identification. This will not
only permit a more precise harvest management, but also better broodstock management
and supplementation evaluation. Currently only hatchery steelhead are marked to
identify hatchery fish.

We recommended that supplementation efforts in the Northwest be annually
summarized. There are several supplementation projects where future information will
be of great benefit. All investigators are encouraged to evaluate the supplementation
projects they are conducting and write up formal reports. We found a heavy bias toward
not reporting negative or unsuccessful results.

INTRODUCTION

We summarized and evaluated supplementation of salmon and steelhead with special
reference to the Pacific Northwest. In some cases projects were reviewed where natural
runs had been extirpated and,were being reestablished or where runs were being
established in areas upstream of barriers. In Alaska, the term "enhancement" is used
when referring to supplementation. However, the Alaska enhancement includes many
fish stocking scenarios which are for increasing commercial harvest opportunities and do
not address supplementing natural runs. We have termed this type of hatchery
production as "harvest augmentation." Harvest augmentation occurs in many other areas
including the Columbia River.

The following definitions are used in this report:

Supplementation - Planting all life stages of hatchery fish to enhance wild/natural
stocks of anadromous salmonids.

Restoration - Planting hatchery products and/or improving habitat to reestablish
extirpated runs or runs that are critically low in numbers.

Enhancement - A general term that describes many stocking and habitat improvement
scenarios used to improve fish runs. Enhancement can include supplementation,
colonization, restoration and harvest augmentation.

Colonization - Describes establishing anadromous salmonids in areas where historically
the species was not endemic.

Harvest augmentation - The stocking of anadromous fish where the primary purpose is
to return adults for sport, tribal or commercial harvest.

Rebuilding - Planting hatchery products to augment natural runs of salmon and
steelhead. In this report used synonymously with supplementation.

Hatchery stock - Having been hatched and partially reared in a hatchery or other
artificial production facility.

Wild stock - Naturally reproducing stocks of fish that have not been supplemented or
augmented with hatchery fish.

Natural stock - Naturally reproducing stocks of fish that have been at one time
supplemented with hatchery- fish.

METHODS

The following key species are included in this report: steelhead (Oncorhynchus mykiss),
chinook salmon (0. tshayqtscha), coho salmon (0. kisutch), sockeye salmon (0. nerka),
pink salmon (0. gorbuscha), chum salmon (0. keta), cutthroat trout (0. clarki) and
Atlantic salmon (Salmo salar). Of the above species, we emphasized review of work on
steelhead and chinook salmon. These two species were identified as priority species for
supplementation research work in the proposed Five-Year Work Plan (Supplementation
Technical Work Group, 1988).

We reviewed current supplementation efforts and unpublished literature by making
contact with fishery biologists throughout the study area. Agency projects and annual
reports were reviewed where available. Data were recorded on a standardized form. and
then entered into a computerized database. Appendix A contains specific information on
the individual supplementation projects we reviewed. Although we attempted to contact
all the key workers involved with supplementation in the study area, we undoubtedly
overlooked some individuals. In addition to project reports, research and management
biologists were interviewed to determine their opinions on how to have successful
supplementation.

STUDY AREA

We emphasized the Pacific Northwest in our review of the unpublished literature and
ongoing supplementation work. We included work being done in Oregon, Washington,
Idaho, California, Alaska, and British Columbia. Some limited information is also
included from the Eastern U.S. on Atlantic salmon.

GENERAL OVERVIEW

Anadromous salmonids have been artificially propagated in the Pacific Northwest for
over 100 years. Fishery managers have used hatchery production to maintain fisheries
and to rebuild runs. The question for the Columbia River Basin is "How can hatchery
production be used to rebuild depleted natural runs of salmon and steelhead in this large
altered river system and maintain the genetic integrity of the various stocks and races of
fish?"

During the past 20-30 years, salmon and steelhead hatchery propagation in the Columbia
River has dramatically increased. Raymond (1988) estimated that beginning in 1970 new
hatcheries were then doubling the number of smolts, in the Snake River. While, in the
mid-Columbia River, this doubling number was attained by 1975. Thus, after 1975 the
majority of salmon and steelhead entering the Columbia River, from the Snake and Mid-
Columbia, are of hatchery origin. For the Snake River Basin 80 to 90 percent of

steelhead and 90+ percent of the chinook salmon smolts passing Lower Granite Dam in
recent years, (1988 and 1989), are of hatchery origin.' Also, during the past 20-30 years
wild/natural escapement has declined.

The Columbia River Fish and Wildlife Plan of 1987 established the goal of doubling the
salmon and steelhead runs from 2.5 million to 5 million. A cornerstone of this program
is to fully utilize available habitat to increase wild/natural production. Although we
have been producing hatchery fish for many years in the Columbia River Basin, there
are still many unanswered questions concerning the use of hatchery fish for
supplementation. The 1987 Columbia River Basin Fish and Wildlife Program, Section,
700 (h), recognizes this problem and stated, "Bonneville shall fund research to determine
the best methods of supplementing naturally spawning stocks with hatchery fish,
particularly in the upper main stem Snake and Columbia rivers." This analysis of
supplementation was undertaken to assist in directing which areas of research needs to
be prioritized for supplementation in the upper Columbia River. Priority species are
upriver chinook salmon and steelhead. The Snake River is the drainage of highest
priority.

RESULTS

General

Our review points out the importance of a potential genetic impact from
supplementation with hatchery fish. The concern expressed in the published literature
review (Steward and Bjornn 1990) and from interviews, indicate that hatchery fish
introduction could adversely impact the natural stock.

Researchers are attempting to document any genetic impacts of supplementation.
Procedures which are being used to minimize adverse genetic impacts include:

1. Using a proportion of the adults in the wild or natural run as broodstock.

2. Stocking practices should mirror the natural environment, i.e., size, timing, stocking
density, and donor stock.

3. Limit the density of stocked fish to prevent displacement or competition with
wild/natural fish.

There are different perceptions to which supplementation procedures work. The
adequacy of supplementation procedures vary regionally. Alaska hatcheries produce and

'Larry Basham, Fish Passage Center, Portland, Oregon, pers. comm., March, 1989.

supplement with smolts, where appropriate. The Columbia Basin states are considering
supplementing more with sub-smolts -- fry and fingerling. This can be explained to some
extent by the intent of supplementation. In the Columbia River Basin, much of the
supplementation effort is intended to enhance wild/natural runs. The emphasis in
Alaska is to produce more adults for "harvest augmentation" while protecting wild stocks.
In Alaska, they are trying to separate hatchery introductions from wild populations by
time of return and release locations. Columbia Basin supplementation managers are
trying to match hatchery production with the environmental constraints of wild/natural
populations.

We included 316 projects in our review of the unpublished and ongoing supplementation
(Appendix A). Of this number, 26 were supplementation, as defined on page 1.
Twenty-five of the 26 supplementation projects we reviewed were considered successful
by the principal investigator. Eighteen of the 26 projects were quantitatively evaluated.
Of the 18, 14 are ongoing and four are supplementation evaluation studies. We found
no evaluated projects that had rebuilt wild/natural runs to self-sustaining levels.

Oregon

Background

Oregon waters support natural populations of chinook, coho, sockeye, chum salmon,
steelhead and cutthroat trout. Anadromous waters encompass 50 river and lake systems
in coastal systems or tributaries flowing into the Columbia River (Anon. 1982a). There
is a small run of introduced sockeye in the Willamette River and a small run of natural
chum in Tillamook Bay.

Artificial production of anadromous fish began in 1877 on the Clackamas and Rogue
Rivers (Anon. 1982a). There are currently 34 state fish hatcheries and 3 or 4 private
anadromous hatcheries ("ocean ranchers") operating in the state. The State hatcheries
produced a total of 75 million fish in release year 1988 (Table 1).

Table 1. Oregon's 1988 State hatchery releases of anadromous salmonids (excluding
STEP).

Summer Winter Spring Fall
Steelhead Steelhead Coho Chinook Chinook

3,906,110 3,186,256 12,674,018 11,743,330 43,395,333-

Primarily Columbia River releases.

Oregon has recently taken a major @bold) fishery management step with the adoption of
its natural production and wild fish management policy. Oregon's policy states that the
maintenance of wild stocks is a biological necessity to insure the future abundance of
both naturally and artificially produced runs (Anon. 1990a). Biologists believe that,
despite past stocking practices, distinct stocks of wild indigenous fish are still viable.
Their managers also state that prior to 1960, the majority of hatchery fish released did
not live to reproduce. These failures primarily resulted from improper stocking
practices, i.e., time and size at release; poor quality fish and/or stocking fish poorly
adapted for the environment (Anon. 1982a).

We reviewed 51 projects in Oregon; only 2 were considered supplementation, both were
successful.

Steelhead

Endemic runs of summer and winter races of steelhead occur in Oregon. Winter
steelhead are primarily coastal, whereas the summer steelhead range encompasses
coastal as well as interior streams.

Release size for Oregon steelhead smolts is 5-6 fish/lb (60-90 g; 200-215 mm). Oregon
managers note that larger smolts produce greater adult returns. However, it was also
noted that larger smolts stray at increased rates.

Hatchery philosophy in Oregon over much time (1890-1960) centered around releases of
unfed fry and pre-smolts. These hatchery fish were usually superimposed on healthy
stocks of natural fish in good habitat with ineffective or counterproductive results (Smith
1987). Smith (1987) also noted that outplanting unfed fry and short-fed pre-smolts
probably presents the highest potential for interference with. indigenous fish.

Oregon biologists are currently experimenting with sterilization of summer steelhead in
the Willamette Subbasin to prevent interaction of hatchery summer steelhead with wild
winter steelhead juveniles. The hatchery summers provide a sport fishery while the wild
winter run rebuilds.'

Coho

Coho salmon in Oregon occur primarily in coastal streams and in the Columbia River
(lower river tributaries). Based on historical catch records, one can easily deduce that
the Columbia River once produced at least as many coho as Oregon coastal streams.

'Ken Kenaston, Oregon Department of Fish and Wildlife, Corvallis, Oregon, pers.
comm., April, 1990.

Oregon's hatchery releases have increased from 7.5 million in 1960 to 12 million in 1988
(excluding private releases). Coho production occurs at 18 public and 4 private
hatcheries. Most natural production now occurs in coastal streams. Wild stocks
comprised approximately 46 percent of the ocean harvest in 1969. They comprised only
25 percent for the period 1977-80 (Anon. 1982b). Coho produced in Oregon contributes
to a number of commercial and sport fisheries.

Tbe Oregon coho hatchery program was enlarged in the 1960s, which generated much
optimism. In the late 60s, adult coho fluctuations became prevalent between years. In
1977, coho abundance dropped to the lowest level since 1962. This downward trend in
adult production occurred in spite of increased hatchery production. The theories of why
coho production went the opposite of predictions are numerous. After 30 years of
intensive artificial production, enhancement projects have been unable to equal the
historic level of natural production.

There is currently a downward trend in adult escapements of wild and hatchery stocks in
a time of increasing hatchery smolt releases. Because of this, ODFW has taken actions
to determine the mechanisms responsible for mortality. ODFW addressed these
concerns by designing seven management objectives in their coho management plan
(Anon. 1982b). Several of these include supplementation strategies. Oregon's new
directive is to supplement natural runs with indigenous broodstock as per wild fish policy
and to explore methods to improve hatchery fish.

Oregon recently determined that they can significantly increase densities of juvenile coho
at the end of the summer rearing period in most streams. However, releases of hatchery
pre-smolts has reduced the density of wild juvenile coho by 40-50 percent (Solazzi et al.
1983). Stocking hatchery pre-smolts produced a net loss for adult returns (Nickelson
1981). The results showed that hatchery pre-smolts should only be stocked in habitat
that is greatly underseeded.

Release size for coho vary between 35-38 g (12-13 fish /lb) for hatcheries with survival
rates less than two percent. When survival is greater than two percent Oregon managers
recommend releasing 23-25 g (23-25 fish/lb) fish. Size at release becomes less critical in
years with high ocean upwelling (Johnson 1982).

Chinook

Fall - The fall chinook salmon of coastal Oregon are healthy and populations are as high
or higher than at anytime in the last century. The landings during 1986, 1987, and 1988
have never been higher during the 70 years that they have been activity fished in the
ocean (Nicholas and Hankin 1989). The complexities of natural processes make it
impossible to state for sure how this happened. However, one sure statement is that
hatchery programs were not responsible. The vast majority of coastal rivers are presently
supporting wild chinook populations at levels equal to anything in the past century

(Nicholas and Hankin 1989). Oregon biologists believe that the credit belongs to the
natural healing, in the past three decades, in many lower main stem rivers and estuaries.
The recovery of coastal chinook salmon has occurred with little or no "tweaking" from
agencies. The famous Elk River study concluded that wild and hatchery systems were
only weakly compatible. These data were collected over 20 years from a hatchery that
was meticulously managed to mirror the wild run. This study makes the point, "hatchery
and natural production systems could coexist if hatchery management practices take
extraordinary care not to reduce the productive capacity of the ecosystem" (Nicholas and
Downey 1989). Based on the results of the study, we conclude that coastal chinook
salmon stocks are healthy and productive because they have productive habitat and have
not been affected by hatcheries.

Sprin - Oregon's spring chinook management primarily focuses on releases of smolts.
Outplanting oversize smolts has generated excessive returns of subjacks and increased
straying (Smith 1987).

The Willamette River historically produced the major portion of the run in the Columbia
Basin. Dam construction 'and years of habitat degradation has reduced the wild run
contribution to a small percentage of the spring chinook salmon return. Approximately
95 percent of the adult return are from hatchery releases. Evaluation of the status of
wild stocks of spring chinook salmon in the Willamette Subbasin has not been
completed.

Spring chinook salmon supplementation evaluation programs statewide are inconclusive.
However, smolt (180-190 mm) releases have produced the most successful adult returns.

STEP

Oregon's Salmon Trout Enhancement Program (STEP) recruits the services of volunteer
citizens to assist with habitat improvement projects, population and spawning surveys,
and strearnside hatch boxes. The STEP program began in 1982 and in 1988-89 the hatch
box segment released a total of 2.6 million salmonid fry (Table 2).

Table 2. Total salmonid fry released in 1988-89 Oregon STEP program.

Sprin Chinook Fall Chinook Coho Winter Steelhead Chum Cutthroat

168,023 571,372 1,035,223 686,653 23,612 113,076

This program involves individuals and conservation groups throughout the state;
however, coastal streams provide the major production.

Prior to STEP, Oregon biologists could not document substantial adult return from fry
releases. While STEP evaluations are incomplete and difficult to document, the adult
contributions are disappointing at best.

Summary

Oregon placed much emphasis on coho enhancement in the 1960s and 70s with little
success. While coho was in the limelight, coastal fall chinook received little or no
enhancement attention. However, coastal fall chinook rebounded to near historic levels
when left to fend for themselves. Protection and healing of mainstream rivers and
estuaries probably deserve most of the credit. The fact that healthy populations of fall
chinook reestablished themselves when provided adequate habitat deserves a closer look
by supplementation proponents.

The STEP citizen volunteer program focuses primarily on fry releases. Early evaluations
have shown disappointing adult returns.

Biologists have documented that larger smolts result in greater numbers of returning
adults. Also, they have documented that hatchery fish can adversely affect wild stocks.

Since there is a preponderance of evidence on the inadequacies of rebuilding runs with
hatchery fish, Oregon recently established a new natural production and wild fish
management plan. It is too early for the results of this program to be obvious.
However, using indigenous wild/natural broodstock for hatchery programs certainly must
be evaluated.

Washington

Background

Anadromous fish runs in Washington include chinook, chum, coho, sockeye, pink salmon,
steelhead, and cutthroat trout. Systems that support anadromous runs include tributaries
to the Columbia River, coastal systems, and Puget Sound.

Artificial production of anadromous salmonids in Washington is conducted by state,
federal and tribal hatcheries. Over 340 million fish were released in Washington in
1987, (Table 3).

We reviewed 129 projects in Washington; 3 were considered true supplementation, only
1 of these was evaluated.

Table 3. Numbers of anadromous salmonids released in Washington in 1987.

Winter Summer Fall Spring
Steelhead Steelhead Chinook Chinook Coho Chum

1,803,646 3,349,917 139,359,630 17,896,634 88,363,656 90,171,973

Steelhead

The Washington Department of Wildlife (WDW) manages the steelhead runs in
Washington. The WDW raises smolts almost exclusively and more than 6 million are
released annually. This stocking effort is mainly to increase harvestable numbers, not to
rebuild natural or wild runs. The operational procedures of WDW hatcheries have
created a separation between the run timing of hatchery produced winter steelhead and
naturally produced winter steelhead. They are presently managed as separate runs. The
early run consists primarily of domesticated hatchery stocks and the later run primarily
wild stock.

While wild steelhead broodstock are not normally,used in WDW hatchery programs,
some winter steelhead programs do utilize wild/natural fish. Some examples include
ongoing programs on the Wynoochee and Skookumchuck Rivers (tributaries to the
Chehalis system), the Nooksack River in northeastern Puget Sound and the Soleduck
River on the north coast. Recently, wild/natural broodstock have also been used on the
Humptulips, Satsop and Sauk Rivers. These programs have been a mixture of true
supplementation and harvesf augmentation. Unfortunately, the supplementation
programs were not rigorously evaluated. The contribution of the hatchery
supplementation to the overall return and especially to the spawning escapement was not
determined. In areas where wild stock was not incorporated, the intent was to separate
wild and hatchery fish.

Escapement data for wild summer steelhe.ad is less detailed although the Toutle, Wind
and Wenatchee systems have shown favorable responses.

Many WDW biologists believe that wild winter stocks are responding favorably to the
current management practices. In the Kalama River, 58 percent of the total winter
steelhead run consists of wild fish. The Elwha River, which is completely blocked by the
Elwha Dam at River mile 5.3, averages only 14 percent wild fish in the total run.

Since 1984 marked hatchery fish are stocked in areas where the wild run is known or
strongly suspected (where definitive data are unavailable) to be underescaped. In these
areas fishing regulations require the release of all unmarked fish.'

There is mixing of wild and hatchery stocks and WDW estimates that 44 percent of the
wild summer steelhead returning to the Kalama River are the direct offspring of
naturally spawning hatchery fish. The WDW has also found that in the Kalama River,
wild summer steelhead appear to be 8.6 times as effective as hatchery fish in producing
adult returnees (Leider et al. 1989).

Survival rates for hatchery winter steelhead range from 16.9 percent for the 1984 brood
year in the Quillayute River to 0.21 percent for 1980 brood year in Cook Creek, tributary
to the Quinault River. An average return rate for hatchery winter steelhead is 5.3
percent (based on data on smolt return rates for nine western Washington rivers).

Salmon

The Washington Department of Fisheries (WDF) manages most of the salmon runs in
Washington. State salmon programs are developing guidelines that will give the
supplementation programs management direction. These guidelines will allow WDF to
document, plan, coordinate, and evaluate ongoing and future activities. They are
currently attempting a more focused evaluation on drainages managed as natural; i.e.,
Gray Harbor, Queets, Quillayate, Skagit, Snohomish, and Stillaguarnish Rivers.

Hatchery management programs are conducted by the state in South Puget Sound
drainages. Most of these drainages are supplemented to meet higher salmon harvest
rates, maximize seeding and realize hatchery goals. These programs are primarily
operational with little or no evaluation. Harvest augmentation is a management goal in
many of these programs.

Within Washington, off station releases accounted for 22 percent of all releases by state
and federal hatcheries in 1985 and 1986 (Anon. 1987a). This amounted to more than
154 million salmon, 60 percent coho, 26 percent chum, 13 percentfall chinook, and 0.4
percent spring chinook.

In some instances where the chinook runs have declined they are utilizing hatchery fish
in an effort to rebuild runs.

Wild broodstock programs have been attempted with chinook and coho. WDF had
problems with wild broodstock in hatchery production situations. Wild coho broodstock

'James Nielsen, Washington Department of Wildlife, Olympia, Washington, pers.
comm., August, 1990.

had low fry-to-smolt survival. The Stillaguamish River summer chinook program is
currently set up to incorporate wild broodstock. The program is also shifting from fry
plantings to smolt plantings with higher survival rates.

Chinook - The majority of supplementation work on chinook in Washington is being
conducted by Indian tribes; outplanting approximately 9,000,000 juvenile chinook
annually. The main purpose of this outplanting is to enhance or establish a fishery.
Most of the fish are stocked as fingerlings ( > 7,000,000), with survival rates for fingerling-
to-adult ranging from slightly less than 1.0 percent to 0.1 percent. Outplanted smolts
have slightly higher survival rates, estimated at around 1.0 percent (Appendix A). The
Yakima Enhancement Study documented survival for wild chinook smolts-to-adults at 4.4
percent in 1983, compared to only 0.05 percent for hatchery releases. Trapped
outmigrating smolts had a higher survival rate for those fish that were acclimated and
volitional released. However, the survival to adults was the same as those not
acclimated (Fast et al. 1988).

Summer chinook salmon are managed primarily for natural production in the
Wenatchee, Methow, Okanogan, and Similkameen Rivers.

One negative aspect of supplementation recently described was the "pied piper" effect of
planting hatchery fish on wild fish. Hillman and Mullan (1989) found that hatchery
releases of age-0 spring chinook salmon in the Wenatchee River "caused" 38 to 78
percent of wild chinook and 15 to 45 percent of wild age-0 steelhead to join hatchery
migrants unless wild fish could not see them. This early migration of wild age-0 salmon
and steelhead was considered a loss to production.

Chu - Most chum supplementation efforts in Washington are concentrated in South
Puget Sound and its small drainages. Like chinook, a number of Indian tribes are
conducting supplementation work to enhance or provide a fishery. Review of the
database (Appendix A) revealed that within Washington over 20,000,000 chum fry are
outplanted annually with 0.07 to 1.0 percent return to hatchery.

Coho - Coho fry are widely stocked in many small streams in Washington with no
separation or differentiation made between hatchery and wild fish. Over 92,000,000
juveniles were outplanted, in 1985 and 1986 combined, to augment harvest with little or
no evaluation. Releases of 395,800 yearlings to the Nisqually River has realized a 10-14
percent return to the fishery (Appendix A). Fry outplants in the Chehalis Basin are
2
estimated to be 0.05 to 0.09 percent to catch as adults, depending upon stock.

2Rick Brix, Washington Department of Fisheries, Montesano, Washington, pers.
comm., April, 1990.

The )NDF collected wild broodstock for rebuilding coho runs on the Quillayute, Hoh and
Queets, River System. They have estimated that cost per spawned female averaged $330.
Juvenile fish are reared to fry, then restocked into systems that are below full seeding
levels. The limited data indicates low survival from fry planting to smolt emigration.
This method produced a net loss of smolt production, compared to allowing the adults to
spawn naturally (Anon. 1987a).

WDF has outplanted yearling coho in Grays Harbor and Willapa Bay. This was used to
reduce hatchery surplus and improve wild production. However, releases of yearlings
were not cost effective and was discontinued.

Summary

Supplementation projects may detrimentally impact other anadromous and resident
salmonids. A coho enhancement project in Puget Sound was at least circumstantially
linked to a major decline (50 percent) in the pink salmon run in a nearby river. This
evidence is substantiated by statistics that show the rest of Puget Sound pink runs
increased by 38 percent for the same period (Ames 1980).

Steelhead management in Washington has benefitted from the marking of hatchery
produced fish. This immediate sight identification of hatchery and wild fish allows
implementation of selective fishery regulations needed to protect underescaped wild
runs. Further separation of hatchery and wild fish is realized by a difference in run
timing. Temporal separation allows managers to collect hatchery broodstock and limit
spawmng'interaction between wild and hatchery fish. Return timing is also useful in
commercial harvest management. Hatchery fish can be fished at a high rate without
adversely impacting wild runs.

Idaho

Background

Idaho stocks of anadromous fish are in a very depressed state. Restoration more
accurately describes Idaho's efforts, which focus primarily on chinook salmon and
steelhead. Historically, Idaho supported runs of steelhead, sockeye and coho salmon as
well as three races of chinook salmon; spring, summer and fall. Hydroelectric dams,
habitat degradation, and overfishing have contributed to the decline of Idaho's
anadromous fish run. Coho salmon no longer enter Idaho and can be considered
extirpated from the state. The last coho to pass Lower Granite Dam was a single adult
in 1986, and only two fish passed in 1985. Sockeye salmon are now being considered by
the National Marine Fisheries Service for endangered or threatened species designation
in the upper Snake River. In 1989, only two adult sockeye salmon passed Lower Granite
Dam. Thus, sockeye. may also be extinct in Idaho. Fall chinook salmon are not being

actively managed in Idaho. The Snake River, from below Hells Canyon Dam
downstream to the confluence of the Clearwater River, is the only area where there are
still significant numbers of fall chinook in Idaho. 'ne Washington Department of
Fisheries, who share management responsibilities on this section@ of the'Snake River,
started a monitoring program on fall chinook for this river section.

Idaho is primarily managing three groups of anadromous fishes; summer steelhead,
summer chinook salmon, and spring chinook salmon. Steelhead and spring chinook
salmon receive most of the management emphasis. In 1989, over 23, million hatchery
fish were released above Lower Granite Dam on the Snake River. Most of these
hatchery fish originated from production facilities located in Idaho. Some came from
Oregon's Grande Ronde and Imnaha River systems. Of the 23 + million, 9.6 million
were spring chinook and 9.9 million were steelhead -- the 2 major hatchery species
reared in the state.

We reviewed 10 projects in Idaho; 2 were considered true supplementation, neither of
them was evaluated.

Steelhead

The potential Snake River steelhead run, based on run strength from 1954-1967, was
estimated for the Lower Snake River Compensation Plan (LSRCP) as 114,800 (Herrig
1990). In 1988, 99,714 steelhead were counted over Ice Harbor Dam. Although this
number is approaching the LSRCP goal, it is estimated that 70-80 percent of the
steelhead run returning to the Snake River are hatchery fish.'

Adult returns to the Snake River above Lower Granite in the past three years (1986-
1989) have demonstrated a greater survival of wild fish over hatchery fish. Data for
steelhead indicate that 20 to 34 percent of the adult fish crossing over Lower Granite
Dam are wild. These returns are from an estimated 10 to 18 percent wild smolts passing
Lower Granite Dam (Koski et al. 1990). This indicates as much as a two-fold survival
advantage of wild/natural steelhead sm-olts above Lower Granite Dam.

Idaho Fish and Game's Anadromous Fish Plan (Anon. 1985) established goals of
returning steelhead and salmon. Steelhead adult returns indicate that the state is
nearing their goal of a smolt-to-adult survival of 2 percent for wild/natural and 1 percent
for hatchery fish. However, the total number of wild/natural fish returning to Idaho is
considered well below carrying capacity of the available habitat.

Idaho is in a very large hatchery program. Most of the stocking and outplanting has
been done with smolts. Most smolts have been released at hatchery racks and have been

'Larry Basham, Fish Passage Center, Portland, Oregon, pers. comm., April, 1990.

used for mitigation, harvest augmentation, and broodstock development.
Supplementation of wild/natural runs has recently been receiving more emphasis. In
recent years, hatchery fish have been outplanted into streams. This program was usually
the result of extra hatchery production. Evaluations are underway on some of these
programs, including the South Fork of the Salmon and South Fork of the Clearwater
Rivers. Evaluation entail late summer fry and yearling snorkel counts primarily.

The Pahsimeroi River was one of the earliest locations where steelhead were outplanted.
This program introduced runs from the mid-Snake River to this tributary on the Salmon
River. Introducing the mid-Snake River run was made necessary by the construction of
three dams in the Hells Canyon section of the Snake River. These dams provide no fish
passage. Returning adult steelhead are collected at the Pahsimeroi trap, but all natural
fish and some hatchery fish (to total one-third of run) are released upstream for natural
spawning. Adipose fin clips permit separation of hatchery fish and wild/natural fish. All
hatchery steelhead are adipose fin clipped in Idaho. The Pahsimeroi River project
releases approximately 900,000 smolts annually with an estimated adult return to Idaho
2
of 1.18 percent. Hatchery fish make up approximately 93 percent of the sportsman
catch on the Salmon River.' Sport fishery regulations require that all wild/natural
steelhead (those with an adipose fin) be returned to the river.

Chinook

Sprin - Historically the Snake River system produced most of the spring chinook salmon
in the Columbia River Basin (Fulton 1968). Today this run is only a remnant of what
used to occur. Ile LSRCP spring-summer adult goals for the Snake River were
established using the 1954-1967 counts at Ice Harbor Dam. The highest count was used
as the potential production for the Snake River. For spring-sumn-ier chinook salmon, the
potential run was estimated at 122,200 adults (Herrig 1990). In 1988, the spring chinook
salmon returning upstream of Ice Harbor Dam, the first dam in the Snake River, totaled
34,394 (Anon. 1989a). It was estimated that up to 80 percent of these spring chinook
were hatchery fish.

With very limited data, estimates were made that less than 10 percent of the chinook
4
salmon smolts passing Lower Granite Dam are wild. Data on the separation of
wild/natural from hatchery fish are being collected at upriver dams on the Snake River.

2Kent Ball, Idaho Department of Fish and Game, Salmon, Idaho, pers. comm.,
January, 1990.

3ibid.

4Basham, p. 13.

For spring chinook, the survival of wild fish may be as much as three or fourfold greater
than hatchery fish. For instance, the Idaho Department of Fish and Game has estimated
wild spring chinook smolt survival to adult in Marsh Creek at 1.2 percent back to Idaho
with good flows at Lower Granite Dam. Rapid River Hatchery spring chinook salmon on
the other hand recorded smolt-to-adult survival of 0.3 percent with good flows at the
dam.5 Hatchery returns of 0.3 percent on good flow years and 0.03 on low water years
indicates that adequate flows are necessary to enhance upriver stocks.

Within the last few years, a number of satellite fish rearing stations have been
established in the Clearwater and Salmon River drainages (both tributaries of the Snake
River). These satellite stations are used for trapping adults and also for partial rearing
of juveniles. Satellite stations are programmed to augment the wild/natural runs present
in some of the tributaries. Evaluations on the effectiveness of the satellite stations in
Idaho have not been determined, primarily because of the relative newness on the
program. However, escapement data and snorkeling counts of yearly fish are being
documented.

Summer - Supplementation of both spring and summer chinook salmon is a relatively
new program in Idaho. Summer chinook salmon are supplemented primarily on the
South Fork of the Salmon River. McCall Hatchery, which started releasing summer
chinook smolts to the South Fork in 1980, has produced significant numbers of smolts.
The goal of that facility is 1 million smolts per year. During 1988 and 1989 1,060,400
and 975,000 summer chinook smolts were released into the South Fork from McCall Fish
Hatchery. The program in the South Fork entails a weir on the stream where the adults
are trapped and eggs are taken. One-third of the fish are taken for hatchery production
and the other two-thirds are passed upstream for natural production. Return rates from
coded-wire tagged summer chinook salmon'released at McCall Fish Hatchery indicate a
smolt-to-adult survival of 0.80 percent for brood year (BY) 1981, 0.44 percent for BY
1982, and 0.46 percent for BY 1983 (Herrig 1990).

Idaho Department of Fish and Game removed natural barriers to allow passage of adult
chinook salmon to Johnson Creek, a tributary to the East Fork of the Salmon River.
Summer chinook fry were outplanted annually from 1986 to 1989. In the fall of 1889, 15
chinook redds were counted above the removed barriers. Stocking of Johnson Creek is
planned to be continued until natural spawning of adults seed the area adequately.

Summary

Idaho is workinglo rebuild runs of summer steelhead, spring and summer chinook
salmon in the Snake River Basin. Some streams aredesignated wild streams where no

-'Charlie Petrosky, Idaho Department of Fish and Game, Boise, Idaho, pers. comm.,
February, 1990.

hatchery fish are planted. These are the Middle Fork of Salmon, South Fork of Salmon,
and Selway Rivers. Outplanting is also restricted in other areas. The marking of all
hatchery steelhead has aided Idaho managers in evaluating hatchery programs and in
documenting the status of wild steelhead. Steelhead smolt-to-adult survival goals of 1
percent for hatchery fish and 2 percent for wild fish are being achieved. However, the
numbers of wild fish are less than needed for natural habitat seeding.

Spring chinook salmon runs (hatchery and wild stocks) are very depressed in Idaho.
Hatchery supplementation, to date, has not succeeded in rebuilding natural runs.
Managers are not getting close to their goal of returning 0.8 percent for hatchery fish.
Right now most hatchery fish returns are nearer 0.2 percent or only 25 percent of the
goal.

California

Background

Anadromous salmonids native to California are chinook, coho, sockeye, pink, chum
salmon, steelhead, and cutthroat trout. Historically, chinook salmon and.steelhead runs
were widespread and abundant throughout the state. Habitat degradation, dam
construction, water developments, watershed alteration, and overfishing contributed to
the decline of salmonids throughout the state.

Hatcheries-were built to mitigate for these losses and are operated by the California
Department of Fish and Game (CDFG) and U.S. Fish & Wildlife Service (FWS). Eggs
were obtained from various California and out-of-state sources to reestablish or
supplement dwindling stocks. The mixing of non-endemic stocks throughout California
have likely altered the composition of distinct gene pools. Despite this, hatchery
production efforts have either maintained or increased spawner escapements in many
waters. Anadromous fish stocking in California is in a restoration phase. They are also
in'a harvest augmentation phase to provide fish for commercial, sport, and tribal harvest.

During the past two decades, private groups have become involved in habitat restoration
projects. Private propagation programs have expanded, particularly in affected areas
where state involvement was minimal or lacking.

The federal and state management agencies, and private groups have all focused on the
importance of restoring fall chinook salmon and winter steelhead. These two species are
receiving the highest attention in both habitat rehabilitation and supplementation efforts.
In coastal areas where coho runs prevailed historically, interest has increased in
reestablishing these stocks. The distributions and abundance of sockeye, pink, and chum
salmon are so limited that propagation efforts for these species has not been practical.

Government and private efforts are attempting to rebuild salmonid runs through stock
management, supplementation, and habitat rehabilitation programs. Although efforts are
ongoing to restore wild spawning populations, the major emphasis is the production of
hatchery fish for harvest augmentation. With this emphasis, the rebuilding of wild stocks
may be limited to some coastal waters and a few subbasin streams within California's
major river systems.

The role of supplementation may become more crucial in California if wild runs of
chinook salmon, coho salmon, and steelhead continue their statewide declining trends.

We reviewed 75 projects in California; 6 were considered true supplementation, only 3
were evaluated.

Steelhead

Steelhead are widely distributed throughout California. The majority of California's
stocks from the larger river systems (Sacramento, Klamath/Trinity) are augmented or
sustained by hatchery operations. Within these basins and in other coastal streams,
numerous waters have remnant or depressed runs of wild winter stee'lhead. The winter
run is the dominant form in California. The Middle Fork of Eel River has the only
native Tun of summer steelhead in the state. This native stock is not supplemented. A
Washougal River (Washington) stock of summer steelhead was introduced into the Mad
River and has been established as a small naturally spawning run. In some years these
adult fish enter the Mad River Hatchery and are propagated independently from winter
steelhead.

Steelhead propagation ranks second to the chinook salmon for all anadromous salmonid
releases. The CDFG and FWS are the main producers of steelhead. The Indian tribes
do not propagate steelhead.

Coleman National Fish Hatchery (NFH) raises about one million winter steelhead
annually. These fish are released as yearlings on-site and off-site (downstream or
estuarine). Contribution rates for on-site releases ranged from 0.10 percent to 0.25
percent, and 0.10 percent to 0.50 percent for off-site releases! The Forest Service
operates two spawning channels, Kelsey and Indian Creek. -Although intended primarily
for fall chinook salmon, these channels are also utilized by steelhead and coho salmon.

Except for the Merced River Fish Facility, winter steelhead are raised in every CDFG
anadromous hatchery. The estimated annual production is about 4.5 million from these
facilities. The steelhead are released as yearling smolts. Release strategies vary by

'Gene Forbes, U.S., Fish and Wildlife Service, Anderson, California, pers. comm.,
March, 1990.

facility and also in response to the continuing drought. In wet years, in the Sacramento
River system steelhead are trucked to the San Francisco Bay estuary. The on-site
steelhead releases from Mokelumne River Fish Hatchery also serve as put-and-take
fishery, while the off-site releases are trucked to Rio Vista (delta area) or the estuary.
Reliable return rates to the Sacramento River Basin hatcheries were not available.
However, based on results achieved with chinook salmon, off-site (downstream or
estuarine) releases are assumed to yield higher ocean and inland returns.

Private programs (includes county and local projects) produced 338,089 steelhead in
1989. The largest programs were (average annual production): Rowdy Creek Fish
Hatchery, 75,000; the Mendocino County Fish & Game Commission, 70,000; Monterey
Bay Salmon and Trout Project, 45,000; and Gualala River Steelhead Project, 30,000.

Chinook

Winter chinook salmon are known only to the upper Sacramento River and this race is a
federally listed threatened species. Coleman NFH represents the only entity propagating
2
winter chinook. Only one adult pair was spawned at Coleman in 1989.

Spring chinook salmon are native in the Klamath and Sacramento River Basins and are
represented by hatchery and wild stocks. The status of the wild stocks are not well-
known and may be tenuous. The South Fork Trinity River spring chinook salmon
abundance has declined and this geographical stock may become a candidate for state
listing as a threatened species.

Fall chinook salmon are the dominant anadromous salmonid in California. The CDFG
and FWS are the largest producers of fall chinook salmon, annually releasing
approximately 30 million and 16 million juveniles, respectively. The U.S. Forest Service,
U.S. Bureau of Indian Affairs, various Indian tribes, and private groups also propagate
fall chinook salmon. Private groups produce over 1 million fall chinook annually (Table
4).

Federal and state hatcheries commonly truck their releases, particularly in the
Sacramento River system. Trucking reduces fish loss at numerous water pumping
stations and diversions. Sacramento River fish are usually trucked to San Francisco Bay
or the river delta. Another outplanting technique used to enhance survival is to divide
release groups and plant into adjacent drainages or different locations within the same
drainage. Outplanted and trucked release chinook groups have exhibited higher survival
than those released on-site. Private programs have also experienced higher ocean
contribution rates and inland return success from yearling-sized releases rather than
fingerling releases.

2ibid.

Table 4. Estimated releases of anadromous salmo nids from private California projects
(permit and contract categories) during 1989.

Fall Chinook Coho Winter Steelhea Cutthroat

Rearing
Independent production 186,350 77,225 76,310 500
Eggs from CDFG 163,000 - 13,999 -
Ocean Pen-rearing 51,082 - - -
Natal stocks
Yearlings 246,189 188,956 247,780 14,000
Smolts 479,712 - - -

TOTALS 1,126,333 266,181 338,089 14,500

Natal stocks releases are progeny of broodstock taken from natural populations.

A late fall chinook population occurs in the upper Sacramento River and is propagated
auColeman NFH. This late fall population may be declining in abundance.

Coho

Coho salmon utilize coastal streams for spawning. They are native to the Russian,
Klamath, and Eel Rivers, and other coastal streams. In contrast to the known historical
status and distribution, the present wild populations are remnant. The status of some
stocks are uncertain.

Coho are propagated by CDFG and private groups. Federal agencies and Indian
Nations are not propagating coho salmon in California. In recent years, CDFG has
annually released about 1 million coho yearlings into state waters. The CDFG operates
the Noyo River Egg Collection Station on the South Fork Noyo River. Eggs taken from
this station have been used to supplement or reestablish coho runs to other coastal
waters.

Prairie Creek Fish Hatchery (PCFH) releases about 100,000 coho annually and
represents the largest level of production from 3a non-CDFG agency. Recent adult return
rates to PCFH for coho salmon was 3 percent. Tle city of Arcata rears coho salmon
and steelhead in a wastewater marsh aquaculture project. The yearlings are then

3Steve Sanders, Humboldt County, Orick, California, pers. comm., February, 1990.

released into a stream adjacent to the marsh. Coho releases average 5,000 annually and
4
adult returns range from about 0.1 percent to 0.3 percent.

The 1989 coho salmon production from private projects (including county and local
programs) contributed 266,181 yearlings to California waters. The Humboldt Fish
Action, Council (HFAC), and the Monterey Bay Salmon and Steelhead Project are the
two largest private coho producers, releasing about 25,000, and 23,000 yearlings annually,
respectively. The HFAC's coho releases contributed an estimated 0.2 percent to the
1989 ocean fishery, the inland recovery rate was also 0.2 percent.5

Coastal Cutthroat Trout

The coastal cutthroat trout occurs in coastal waters from the Eel River drainage and
northward. The present range may be identical to the known historical distribution.
However, while their abundance has declined considerably, existing populations are
believed to be stable, There are about 120 streams with cutthroat, comprising about 700
miles of habitat (Gerstung 1981). Although cutthroat trout are not as popular as other
anadromous species, increasing harvest pressure on the other species may elevate the
importance of cutthroat as a sport fish.

The Fisheries Department of Humboldt State University (HSU) has begun propagating
anadromous coastal cutthroat to enhance sport fishing in local Humboldt County
lagoons. The first release of 14,000 juveniles is scheduled for the spring of 1990. They
are reared at the HSU hatchery then trucked to release sites. Humboldt County and
HSU are the only entities propagating coastal cutthroat in California. About 500
cutthroat trout are released annually by Humboldt County. These cutthroat are released
as yearlings and will hopefully contribute to the local inland sport fisheries.

Summary

There is considerable interest in supplementation, especially among private groups.
Consensus among private groups expressed a need for additional programs, to
rehabilitate waters which formerly produced salmonids. They also voiced the need to
work together with the state to meet common objectives. The majority of the state
personnel interviewed were in agreement with the private faction.

4David Hull, City of Arcata, Dept. of Public Works, Arcata, California, pers. comm.,
February, 1990.
5Jud Ellinwood, Humboldt Fish Action Council, Eureka, California, pers. comm.,
March, 1990.

One concern that was apparent among virtually all groups contacted was the issue of
inter-basin transfers of salmonid stocks. Although most people were aware of the
biological implications, some felt that inter-basin transfers were necessary to attain their
goals. Others expressed a need to end all inter-basin transfers of all life stages.
Although CDFG has a formal policy against inter-basin transfer of stocks, this
supplementation review indicated that the practice is common and widespread. The
CDFG has transferred stocks for restoration purposes to establish and maintain runs.
Some private programs have received both endemic and non-endemic eggs from CDFG,
particularly in waters with depressed or extirpated stocks.

The state's intent ha@ been to supplement and expand dwindling or geographically extinct
wild stocks. However, a formally organized statewide active program to increase wild
stocks (through supplementation) was not apparent from the state personnel interviewed.
Maintaining high production levels is the driving force within the hatchery management
system. Many personnel from all sectors expressed concern about the proper levels
(density) of stocking. Additionally, various measures to promote the survival and return
of hatchery stocks (such as trucking juveniles downstream) have been successful.
However, there is little done to aid natural production.

Although private projects are also motivated to maximizing their production, they have
not deviated from their grass-roots objectives of rebuilding local remnant stocks. The
private projects are limited by economics; the materials, personnel, technology, and
funding necessary to define the capability and nature of these projects. California's
private sector has the potential to increase present levels of supplementation with
additional funding.

Guidelines among public agencies and private groups on the biologically appropriate
levels of production and supplementation are lacking. This problem needs to be
addressed to promote an organized and scientifically sound approach to rebuilding
salmonid stocks.

Alaska

Background

Alaska has two entities doing enhancement of salmon and steelhead, private non-profit
(PNP) hatcheries and the Alaska Department of Fish and Game, Fisheries
Rehabilitation Enhancement and Development (FRED) Division hatcheries. PNP
hatchery programs provide a structure for fishermen to be involved with the commercial
fisheries programs. The PNP hatcheries are supported by Regional Aquaculture
Associations and produce fish for commercial harvest. There are seven regional
aquaculture associations in Alaska. The PNP rear pink, chum, coho, chinook and
sockeye salmon at their hatcheries. In 1988, PNP hatcheries took more than 1 billion

eggs and released 819 million fry and smolts (Holland 1989). Most releases were pink
and chum salmon fry, approximately 626 million pink fry and 186 million chum fry. In
1988, there were 22 PNP hatcheries in Alaska. The Regional Aquaculture Associations
are supported by a tax on the commercial salmon harvest (landing fee). They also
market excess fish returning to the PNP hatcheries.

Alaska's FRED Division focuses on the development of new enhancement technology,
hatchery production, technical services, permitting, and habitat restoration and
rehabilitation. ne PNP hatchery program is administered by FRED under a permitting
system.

The FRED system operates 16 hatcheries and several ancillary hatchery facilities. In
1988, FRED hatcheries released 412.6 million fry and smolts of which 407 million were
salmon and steelhead (Holland 1989). Of the total release (1989) 320 million were pink
and chum salmon (Table 5).

Most of PNP hatcheries produce pink and chum salmon with some sockeye, coho, and
chinook. Plans are moving forward to produce more sockeye smolts at some PNP and
FRED operated facilities.

Table 5. Releases of fry and smolts, salmon and steelhead, from Public Non-profit
(PNP) and Alaska Department of Fish and Game, FRED Division hatcheries,
1988. (Holland 1989).

PNP Hatcheries FRED Division Hatcheries
Species Number (x1,000 Specie Number Lx1.000

Chum 186,050 Chum 106,531
Pink 625,820 Pink 213,580
Sockeye 1,000 Sockeye 68,142
Coho 4,720 Coho 14,441
Chinook 2,210 Chinook 4,115
Steelhead 271

TOTAL 819,800 TOTAL 407,080

Biologists are attempting to rebuild or supplement some wild/natural runs of salmon and
steelhead. However, most of the hatchery effort is to increase runs for harvest
augmentation. Fish are released directly from the hatchery or introduced to areas where
the adults can be harvested while wild stocks are managed for escapement. Efforts are
underway to introduce salmon to unutilized production areas where barriers or other
factors have restricted access to fish. New programs will examine means to bring fish

back to areas just for a specific type of harvest - sport, commercial or subsistence. Fry,
fingerling, and smolts are released directly into ocean bays, small streams, lakes or rivers
to key adults back to a terminal fishery.

Alaska's hatchery program is rated quite successful because it is providing more stability
in the commercial fisheries program. In 1987, roughly 25 percent of the total statewide
salmon harvest was from salmon produced by public programs (FRED & PNP). In 1988,
this figure was 24 percent (Hartman et al. 1988). To separate wild from hatchery stocks
in a mixed stock fishery, many hatchery fish are marked with coded-wire tags (CWT). In
some fisheries, hatchery fish are separated by timing into a fishery area and by location
of return. Overall, fisheries management in Alaska is directed primarily for wild fish
escapement with hatchery releases directed for harvest augmentation.'

We reviewed 24 projects in Alaska; 2 were considered true supplementation, both were
evaluated.

Steelhead

Very little steelhead supplementation has occurred in Alaska. No specific evaluation
information was found.

Chinook

Hatchery cbinook salmon programs have not been as successful as some of the other
hatchery programs in Alaska. When comparing adult returns with the Columbia River
system, Alaska does as well or better. Chinook salmon adult returns in the 2-4 percent
range from smolt plants have been common (Dudiak and Boyle 1988). Alaska biologists
expect to get 3 percent or better adult returns for smolt releases of chinook, coho, and
sockeye salmon. Programs to build fisheries in selected areas for chinook salmon harvest
has worked quite well in Alaska. Chinook salmon smolt releases in Prince William
2
Sound return in the 4-5 percent range.

Alaskan biologists use indigenous broodstock almost exclusively for supplementation.
Fry, fingerling and smolts have been outplanted to natural areas. In the Kasilof River,
biologists have stocked chinook salmon smolts into areas with wild stock and noted no
impacts on wild stocks. They did note that survival of hatchery fish was about one-half
of what they thought it should be (Kyle and Litchfield 1989).

'Keith Pratt, FRED Divisions, Alaska Department of Fish and Game, Anchorage,
Alaska, pers. comm., February, 1990.
2Bruce Suzurnota, Prince William Sound Aquaculture Association, pers. comm.,
February, 1990.

Managers in Alaska are doing some lake rearing of chinook with fish from the Gulkana
Hatchery, a Copper River stock. Fed fry are taken out by plane and planted into lakes
in the upper Copper River. This pilot study has just started so no data on survival is
available at this time.

Sockeye

Sockeye salmon are the premier commercial fish with outstanding market value.
Therefore, production has increased in PNP and FRED hatcheries. Early hatchery
programs suffered from chronic losses to IHN disease; however, techniques for managing
around IHN have now been improved. Also, techniques of both lake fertilization and
lake production modelling have progressed so managers can strive for maximum
production from rearing waters.

Sockeye salmon in Alaska are planted into barren lakes or lakes with adult barriers and
to supplement existing stocks. Lakes are usually only a few miles from salt water. A
program of lake fertilization is done following a liminological study to identify needed
fertilizers. Again, natural broodstock are used where possible. Excellent adult returns
have been realized with smolt releases. Adult returns as high as 35 percent were
documented at Big Lake. Biologists are expanding sockeye smolt releases because of the
phenomenal successes.

Following are survival rates of various stocking techniques:

Sockeye stockings of unfed fry into lakes; expecting a greater than 1 percent survival
in the Gulkana River area. Sockeye stocked in Summit Lake of the Gulkana
3
drainage as unfed fry have returned at 0.8 percent as adults.

Some sockeye smolt stocking into Big Lake have adult returns at a rate as high as 35
percent.

Planting eyed eggs in upper Thumb River, a tributary of Karluk Lake, has increased
adult returns to Karluk Lake and spawners to upper 'numb River. Eyed egg survival
to fry is reported as exceeding survivals commonly obtained from natural spawners
(White 1986).

Fingerling sockeye released into Hidden Lake built up the production for the lake. It
was believed spawning area was the limiting factor. Fingerling-to-smolt survival
averaged about 20 percent and smolt-to-adult survival averaged around 15 percent
(Litchfield and Flagg 1988).

3Ken Roberson, Alaska Department of Fish and Game, Glennallen, Alaska, pers.
comm., January, 1990.

Strearnside hatching facilities at Gulkana for sockeye and chinook salmon also appear
to be working exceptionally well. Groundwater from the stream is directed through
large units of Kitoi egg boxes loaded with sockeye and chinook eggs. As fry hatch,
they are washed into a trapping and enumeration area and from there outplanted.
Fry hatch at a similar time as natural spawned eggs. This is a low technology, low
cost method of salmon fry production.

Coho

Coho salmon are stocked into lakes, streams, and net pens for enhancement purposes.
Stocking and enhancement procedures in lakes are similar to the sockeye salmon
supplementation effort. Some limited success has been achieved with coho lake stocking,
but this program is still in the evaluation stage. Also, some coho work is being done
with net pens in the inlets and salt water areas. PNP reports of 15 to 20 percent adult
survival for some coho salmon smolt releaseS.4

Examples of coho salmon adult returns from hatchery releases follows:

Fingerling-to-adult from Seldovia Lake approximately 1 percent (Dudiak and Boyle
1988).

Fingerling-to-adult from Caribou Lake approximately 2-3 percent (Dudiak and Boyle
1988).

Up to 4 percent return from smolts on Homer spit (Dudiak and Boyle 1988).

In the Yukon River hatchery fingerling produced adult returns of 4.0-8.5 percent and
13.4 percent for wild fish (Raymond 1986).

Smolts released from net pens in Prince William Sound returned at a rate in the 15-
5
20 percent range.

Pink and Chum

Pink and chum salmon are released as fry (fed or unfed) and go directly to the ocean.
Releases can occur directly from hatcheries or from other sites where fish migrate
directly to the ocean. Some net pens are used with feeding programs and match release
of fry with plankton peaks. The key to success is to get fish to the estuary at peak
plankton production.

4ibid.

5Suzurnota, p. 23.

In Tutka Bay, Boyle and Dudiak (1986) recorded survival rates of hatchery released pink
salmon fry at 12.5 percent for fed fry and 14.5 percent for unfed fry. Most other releases
have shown a higher return for fed fry. Lower rates near 1-3 percent for unfed fry are
common for both pink and chum fry releases (Kohler 1984; McDaniel et al. 1984).
Feeding fry a few weeks and releasing with plankton peaks contribute to higher survival.
Survival as high as 14 percent were seen, with several groups returning at 8 percent.

Summary

Supplementation in Alaska is primarily what we have classified as harvest augmentation.
Their management scheme is to manage for wild stock escapement and use
supplementation to increase salmon runs for commercial fisheries. In a few cases,
natural sockeye stocks have been rebuilt. Most of the impetus for this rebuilding was for
harvest.

Separating hatchery stocks from wild stocks has occurred by bringing salmon back to
areas where no natural population exist and by separating time of run return.

Ideas that apply to supplementation in the Columbia River Basin include: (a) streamside
spawning and incubation units, Kiotoi boxes, and outplanting of fry, (b) lake fertilization
and fry planting schemes for sockeye, (c) separating hatchery stocks from wild stocks by
place and time of return, and (d) managing for wild stock escapement with hatcheries
keyed to harvest augmentation.

British Columbia

Background

British Columbia (BC) probably comes closer to true supplementation than any area in
the Northwest. Their Fraser River Basin is similar to our Columbia River Basin.
However, BC does not have as many dams and associated fish passage problems. BC's
Salmonid Enhancement Program (SEP) began in 1977 to double their salmonid
production. SEP's responsibilities are divided between two agencies. The Federal
Department of Fisheries and Oceans manages the five species of Pacific salmon.
Steelhead and cutthroat trout are managed by the Provincial Ministry of the
Environment.

SEP supplements natural production by the most natural means and thereby reduces
cost. Currently SEP has a moratorium on new hatchery construction. They concentrate
primarily on using existing hatcheries to incubate gametes from indigenous broodstock.
They employ strearnside upwelling incubation units and groundwater fed side channels to
produce rearing habitat. They also utilize spawning channels to extend the amount of
spawning area available. These channels are of particular value for sockeye, pink, and

chum salmon. The spawning channels also provide rearing habitat for other species such
as chinook and coho salmon.

In the late 1970s, SEP, in its infancy, developed facility targets in a piecemeal fashion.
The present system evolved by dividing the geographic regions into management units.
Each unit reviewed the individual stocks as to the status, ability to manage and capacity
for additional production potential. There are three area planning committees that
develop recommendations, the South Coast Division, Fraser River - Yukon Division, and
the North Coast Division. When a project shows promise, the management unit outlines
the expected economic and social benefits and submits it to the Treasury Board. For
allocation of construction and operating dollars, the project has a goal of 1.5:1
benefit/cost ratio (Hurst and Blackman 1988). Each project uses estimated survival rates
for each type of enhancement strategy and is sized accordingly.

Federal fisheries biologists have increased productivity of lakes and streams by the
application of fertilizers. This technique is used in situations when there are sufficient
sockeye salmon spawners and suitable habitat is available. The fertilization promotes
increased growth of the basic components of the salmonid food chain. SEP also
concentrates on habitat improvements for enhancing salmonid productivity by some basic
stream improvements. These improvements may require physical cleanup, placement of
boulders, planting of streamside vegetation, flow control, and eliminate possible pollution
sources.

We reviewed 18 projects in BC; 9 were considered true supplementation, 8 were
evaluated. One of these projects was considered not successful in contributing to natural
production.

Steelhead

BC's total steelhead hatchery production for 1989 was only 2.4 million fish. These were
planted into 28 systems. Steelhead are released at three life history stages: smolt, parr,
and fry. The strategy of the smolt programs is to grow the smolts as large as possible
(60-100 g or 190-220 mm), then outplant during late April to late May. The smolt-to-
adult survival varied from 1 percent for small smolts to almost 10 percent for 60 g smolts
(BC's program released 800,000 smolts in 1987). They determined that they could gain
30-40 percent smolt-to-adult survival by lower river releases, i.e., tide water. They had
much lower survival for groups released only 10 km upstream. BC's major limitation in
steelhead research is returning adult enumeration.

Parr - BC released 355,000 parr from brood year 1987. They use two strategies for parr
releases, both with 15 g fish (30/lb). This program began in 1987 and the return data
for the Coquihalla River demonstrated a parr-to-adult survival of 2.6 percent. They
expected 3.2 percent parr-to-adult survival. Based on cost comparisons to produce 100

adults BC concluded that if you have the habitat, parr are more cost effective over fry or
smolts.

fr.
y - BC stocks steelhead fry for two primary reasons: colonization - defined as releasing
fry above anadromous barriers, and supplementation - stocking fry in underseeded
stream reaches.

From the 1987 brood year BC released 1.2 million; 2.0 g fry (200/lb) into 28 systems. A
typical release method is by helicopter to enhance dispersal. BC fry stocking began in
the early 1980s. Criteria used for survival of fry-to-smolt are largely dependent on:
1. age at smolting, 2. amount of physically suitable habitat for all life history stages,
3. size of fish released, 4. productivity of different streams, (i.e., total alkalinity can very
from 4 to 200 mg/1), and 5. presence of competitors or predators. Biologists we
interviewed stated that in the early fry programs they overstocked. They used no
prescribed stocking formula in these early programs and the results were disappointing.
BC biologists went back to streams, developed site specific biostandards for stocking
densities, and now release fish at more conservative stocking densities. Now they
consider total usable area rather than the older method of total wetted area. They cite
many examples of overstocking resulting in decreases in growth performance of both
hatchery and wild juveniles. The results from the Coquihalla River are encouraging with
fry-to-adult survival ranging from 0.4 to 1.3 percent. Expected survival was estimated at
1.3 percent (Ptolemy 1986). They measured a fourfold increase in standing crop of
juveniles following the fry released.

Salmon

In release year 1988, the Department of Fisheries and Oceans (DFO) recorded releases
of approximately 530 million pink, chum, coho, sockeye, and chinook salmon (Table 6).
DFO biologists use indigenous broodstock to ensure against stocking maladapted fish.
They release the progeny from wild fish into the parent watershed after adipose clipping.

Broodstock are spawned (streamside) 1:1 male/female ratio and gametes taken to
hatcheries. Biologists verify carrying capacities of life stage to be stocked in terms of
usable habitat before outplanting progeny.

Chinook

In 1988, DFO released 63.6 million chinook salmon of various life stages. Production of
chinook salmon (stream and ocean types) for stocking is primarily through hatchery
operations (federal, provincial, and community economic development programs). These
hatcheries do not recycle broodstock. DFO biologists also develop groundwater side
channels with upwelling incubation for chinook production. These groundwater channels
also provide critical rearing habitat.

Table 6. British Columbia's salmonid production from SEP facilities, 1988 release year.

Specie Juveniles Released EVected Adult Canadian Catch

Pink 62,713,919 1,325,423 7271357
Chum 213,391,888 2,535,674 1,163,013
Coho 18,470,120 1,099,88 i 707,648
Sockeye 171,988,081 2,063,346 812,754
Chinook 63,624,513 895,503 483,376
Cutthroat 238,680 20,584 13,792
Steelhead 2,371,647 45,407 26,944

TOTAL 532,798,848 7,985,818 3,934,884

From SEP 1988-89 update booklet.

Sockeye Chum and Pink

Spawning channels, lake fertilization, barrier removal, and habitat improvements are the
primary enhancement methods for sockeye, pink, and. chum salmon. DFO biologists
recently constructed a new spawning channel at Glendale Cove on Knight Inlet that will
potentially produce 1 million adult pink salmon annually. Channel production has
realized an egg-to-fry survival of 81 percent (Anon. 1989b). The channel addresses
natural low flow problems by drawing water through a pipeline from Tom Browne Lake.

Lake fertilization increases production in the enhancement of sockeye, pink, and chum
salmon. Fertilization takes the place of the thousands of carcasses from spawned out
adults that once fertilized these lakes.

Coho

Biologists from DFO primarily use natural and semi-natural enhancement and secondary
hatchery production to supplement coho salmon stocks. We visited a new construction
site on the Englishman River (Vancouver Island). The Englishman River utilizes side
channel production for the lower river and coho salmon colonization for the inaccessible
reaches. Spawning and rearing channels built in 1988 use groundwater and infiltration
galleries to provide water flows. In areas not accessible to spawners, coho salmon fry
obtained from a nearby hatchery were stocked. For succeeding years, wild stocks from
the Englishman River are the preferred donor stocks.

Eight streams that empty into Baynes Sound have been the traditional backbone of the
Georgia Strait coho sports fishery. However, commercial fisheries and an aggressive
sport fishery targeting on these runs have led to depressed stocks through overfishing.
They became the focus of rebuilding in 1988. It became impractical to manage the eight
streams separately because of extreme exploitation. Biologists now manage them as one
unit with stocks treated as a single gene pool. BC biologists believe the small genetic
differences do not justify managing each stream separately. Also, too few fish return to
attempt separate stock management for each stream. Thirty pairs of wild adults,
collected from the eight streams, provide smolt production. All outplanted smolts are
adipose clipped to facilitate wild broodstock collection in subsequent years using this
management strategy. Fry are never more than one generation removed from wild stock.
The use of wild broodstock each generation in SEP supplementation more than pays for
the additional labor. We believe this procedure may be of benefit in the Columbia
Basin where possible to implement.

Public Participation

BC provides an opportunity for many citizens to volunteer their time in enhancing
salmonids. The SEP sponsors one of the most unique public participation program in
North America. This program provides community advisors, stationed throughout the
province, to give technical and financial assistance. Individuals, clubs, schools, service
organizations, and community groups may apply for this program.

Opportunities for such participation lie in maintaining, restoring, and improving the
stream habitat essential to salmonid production. Through public participation,
enhancement projects also offer a unique opportunity to develop a greater awareness of
the salmonid resource and man's influence on the stream environment.

Summary

In the 13 years since the SEP began, BC biologists have recorded real progress toward
meeting their goals of doubling the runs. Their total budget for 1988/89 was
approximately $42 million. They de-emphasize recycling hatchery broodstock and placed
a moratorium on new hatchery construction. They developed objectives and goals to
utilize natural production and semi-natural production in supplementing their stocks.

It would be tempting at this juncture to dismiss SEP's objectives as unrealistic in the
Columbia Basin. However, their upper Fraser and Thompson River stocks of steelhead
and chinook salmon migrate hundreds of miles inland to spawning grounds. SEP
biologists still practice the same sound genetic principles as with coastal stocks. The
Whitehorse Rapids Hatchery on the Yukon River continues to collect wild broodstock in
view of adult immigrations of 3520 Km (2200 miles). We believe the judicious use of
wild broodstock for BC supplementation work has been a positive factor in their
successes.

We, in the Columbia Basin, should be envious of their management predicament.
Biologists only have to coordinate between two agencies, the Department of Fisheries
and Oceans and the Ministry of Environment, to manage supplementation in BC. The
provincial government manages steelhead and DFO oversees salmon management. They
do not have to run the gauntlet of countless agencies and committees that currently exert
management authority in the Columbia Basin. It appears that BC's bureaucracy may be
down to fighting weight.

New England

Atlantic Salmon Program

This information was obtained from the New England Atlantic Salmon Program Annual
Progress Reports for 1987 and 1988 and the 1989 Annual Report of the U.S. Atlantic
Salmon Assessment Committee (Anon. 1987b, 1988, 1990b). Telephone conversations
with the various program coordinators also clarified overall direction.

Background

Historically, Atlantic salmon thrived in rivers from Maine to Connecticut, with major
runs found in the Connecticut, Merrimack and Penobscot Rivers. By the late 18th
Century, the Atlantic salmon was essentially extirpated from these areas due to the
Industrial Revolution and overfishing. While the Atlantic salmon was never totally
eliminated from all Maine Rivers, their numbers were severely depressed, and by 1872
the federal government began stocking rivers in Maine. During the period 1872-1959,
more than 63,340,000 juvenile Atlantic salmon were released into drainages throughout
Maine.

Today's program receives much of its direction from the Atlantic Sea-Run Salmon
Commission, which was formed in 1947. The overall goal of the program is to restore a
self-sustaining population of Atlantic salmon by the year 2021. The Atlantic Salmon
Program is divided into four major programs involving state and federal agencies, private
industry and conservation organizations. Collectively, about 5.5 million juvenile Atlantic
salmon were released into 15 New England rivers in 1989. The Maine program received
36 percent of the releases, 34 percent Went to the Connecticut River program, 23 percent
to the Merrimack River program and 7 percent to the Pawcatuck River program. The
stocking summary for 1989 is shown in Table 7. From 1980 through 1988, almost 27
million juvenile salmon had been stocked into New England rivers. Almost 50 percent
of the fish released were fry and about 25 percent were age-1 smolts. During this same
9-year-period, 33,486 adult Atlantic salmon have returned to 16 rivers in New England.

Of these returns, 80 percent has been to the Penobscot River in Maine. Ten percent of
the returns to the Penobscot River are from natural production.'

Table 7. Atlantic salmon stocking summary by program in 1989.

Progra FU 0 + Parr 1Parr 1smolt 2Smolt Total

Maine
USA 580,000 430,500 282,200 524,300, 80,200 1,897,200
Canada 66,000 - - - 10,300 76,300

Merrimack River 1,033,000 60,000 88,600 58,200 - 1,239,800

Pawcatuck River - 379,900 35,900 6,400 422,200

Connecticut River 1,242,000 272,900 116,300 221,000 - 1,852,200

TOTAL 2,921,000 1,143,300 523,000 809,900 90,500 5,487,700

Atlantic salmon cannot be harvested in the Connecticut or Pawcatuck Rivers. Fishing is
allowed in parts of the Merrimack watershed. However, there were no reported catches
in 1989. Total catch of Atlantic salmon in Maine was reported at 1,007 fish in 1989, 520
of those were released. The Penobscot River produced 86 percent of the total catch.
An exploitation rate of 10 percent was set to help accelerate the restoration of the
Penobscot salmon run.

In Maine, the Dennys, E. Machias, Machias, and Narraguagus Rivers are designated
"wild" but still receive releases of fry, parr, and smolts. In 1989, they were supplemented
with 270,800 juverffle salmon. Returns to these rivers are believed to be mostly of wild
origin, primarily from natural reproduction, with very few originating from fry releases.
In New England "wild" generally refers not only to fish produced naturally, but also to
fish produced from fry stockings.

While all of the programs receive various life stages of Atlantic salmon, each of the four
programs has a different emphasis. The Maine program is mainly a smolt stocking
program while the Merrimack River receives mainly fry. The Connecticut River program

'Jerry Marancik, U.S. Fish and Wildlife Service, Orland, Maine, pers. comm.,
February, 1990.

receives a combination of fry and smolts and the Pawcatuck River has a parr stocking
program.

We reviewed nine projects in the New England states; two were considered true
supplementation, both were evaluated.

Fry Stocking

Restoration in the Merrimack River relies mainly on fry that are scatter planted into
nearly all suitable rearing habitat. Roughly 250 miles of stream are presently included in
the program. In 1989 and 1988, over 1.0 million and 1.7 million fry respectively were
released in the river basin. The fry stocking goal for the Merrimack River Basin is 1.8
million.

The majority of returning salmon are trapped and held to be used for spawning.
Domesticated captive broodstock and reconditioned kelts are also used to obtain the
number of eggs desired for the program. All fry stocked into Merrimack drainages in
1987 were of Merrimack River origin.

Fry are stocked at 20 to 50 fry per 100 square meter unit depending on the quality of
habitat, etc. Seven index sites are then monitored for growth and survival, condition
factors and water quality.

Since 1982, roughly 40 percent of the adult returns to the Merrimack River have
originated from the fry stocking program. Seventy-four percent of these fry emigrate as
two-year-old smolts. The contribution of the fry program was 66 percent of returns in
1988 and 67 percent in 1989. It should be noted that total fish for 1088 and 1989 was 65
and 84, respectively. These are the first and second lowest full-season totals since
salmon returns to the river were first documented in 1982. The range of adult returns to
the Merrimack for 1983 to 1987 is 103 to 214 with a mean of 137. Total return through
1989 numbers 860. The adult return rate for 1984 fry plants surviving to 1+ parr was
estimated at 0.04 percent. Total return fry-to-adult was 0.005 percent for 1984 releases.
Of the adults returning to the Merrimack, 78 percent return as 2-sea-winters, 18 percent
as 1-sea-winters and 4 percent as 3-sea-winters.

The Connecticut River program utilizes fry releases in its restoration efforts with a
stocking goal of 2.0 million fry. In 1989 and 1988, over 1.2 million and 1.3 million fry,
respectively, were released in the river basin. Minta et al. (1987) found the survival of
"wild" smolts (smolts produced from fry releases) -to-adults was nearly 10 times greater
than hatchery smolt-to-adult return rates for a Connecticut River tributary in 1984.
These "wild" fish comprised 36 percent of the total run. Y. Cote, a Quebec biologist,
found that flow for 30 to 40 days after stocking is a critical factor in fry survival.

Parr Stocking

While Atlantic salmon parr are stocked in a number of locations in New England, they
are mostly incidental by-products that are graded out of one year smolt programs. The
Pawcatuck River program in Rhode Island is an exception in that parr are stocked
almost exclusively. The Pawcatuck program is unique in a number of other ways also.
ne watershed is near the southern extent of the range of Atlantic salmon; therefore, it
is not a typical cold water river, as found farther north. Furthermore, predator species,
abundant in this drainage, exact a heavy loss on salmon fry. The Pawcatuck program is
also the smallest of the four Atlantic salmon programs, hence the smallest budget. For
these reasons, the program has decided that Farr stockings are the most cost effective
method of developing their salmon program. Further problems have developed from
the parental source of these parr. The program currently uses only domesticated captive
broodstock (fish that have never gone to sea) as their egg source. There is evidence that
this strain is inferior to sea run parents (Gibson 1989); thus producing poor return rates
in the progeny. Return rates for the program range from 0.0 percent to 0.009 percent
with a mean of 0.003 percent. Releases in 1989 numbered over 400,000 parr, which is
the largest number of fish stocked into this system since the program began in 1979.

Smolt Stocking

The smolt program is the most successful of the various programs. The Penobscot River
in Maine received over 416,000 smolts in 1989 (47 percent of the smolts released).
Overall adult returns to the Penobscot have ranged from 0.23 percent to 1.32 percent
with a mean of 0.71 percent. In 1989, 2719 fish returned to traps in the Penobscot, 813
were 1-sea-winter fish, 1,864 were 2-sea-winter fish, 4 were 3-sea-winter fish, and 38 were
previous spawners. The Maine stocking program utilizes returning salmon and
domesticated captive broodstock for egg takes. Additionally, returning adults not needed
for egg takes are released to spawn naturally. In 1988, this amounted to 2,141 out of
2,688 fish trapped in the Penobscot River.

The long-term objectives for the Penobscot River are:

1. Achieve an annual production of 185,000 wild smolts.
2. Ensure a minimum of 6,000 adults will be available for spawning annually.
3. Provide a minimum of 2,000 adult salmon for sport harvest annually.

The Connecticut River program also utilizes smolts in its restoration effort with 10 to 32
percent of total releases being smolts. This program released 221,000 and 395,300 smolts
in 1989 and 1988, respectively. The smolt stocking goal for the Connecticut program is

2Mark Gibson, Rhode Island Division of Fish and Wildlife, W. Kingston, Rhode
Island, pers. comm., March, 1990.

590,000. Smolt-to-adult return rates for hatchery smolts released in the Connecticut
River Basin ranges from 0.006 to 0.159 percent depending upon year and location.

Smolts in Connecticut are generally stocked from hatchery trucks via "quick release"
hoses or netted off trucks directly into ponds. In 1989, one lot of coded-wire tagged
smolts (22,500 fish) was placed into a 15-by-15 meter net pen in the lower Connecticut
River. The net pen was towed two kilometers into Long Island Sound where the smolts
were released. The primary purpose of this project is to compare return rates of salmon
that were not subjected to river related mortality. Data on the success of this technique
will not be available for a few years.

Tagged Atlantic salmon smolts and parr are used to help determine the contribution of
the New England Atlantic salmon programs to the ocean harvest. Ta gging also allows
sight identification and a method to ascertain the contribution of various life stages to
the run.

Summary

While adult return rates are generally low for the Atlantic salmon program, it should be
remembered that the program is a restoration effort because of degraded river systems.
Furthermore, the program does not base its success in terms of adult returns, but on
what is learned and the directions then taken. While the progress is slow, it is
continuing to move forward. Wild fry or smolts were found to survive to adults at a
much higher rate than hatchery smolts.

The reuse of kelts for egg taking was a new procedure we have not considered for
steelhead in the Columbia Basin.

River flow at time of fry release seemed to be a factor to consider in the success of fry
plants.

Broodstock that has never gone to the ocean produced inferior results when compared to
sea run broodstock. Again, the genetics of the broodstock should be a factor when
implementing supplementation programs.

Releases of smolts returned more adults than releases of other life stages in the Atlantic
salmon program. The average smolt-to-adult return rate for the Penobscot River is 0.71
percent. However, the ability to establish self-sustaining runs is still being evaluated for
all the programs.

CONCLUSIONS

Supplementation has provided positive results in the following:

a) BC is having success with chinook, coho, and steelhead by using only wild
broodstock and scatter planting the hatchery produced fish through the
supplemented area.
b) BC also concluded that in some instances parr stocking of steelhead was more cost
effective than either fry or smolts.
c) Alaska and BC are having success using strearnside incubation boxes with stream
water diverted through boxes. Fry are scatter planted and spot planted from these
stream incubator systems.

However, when we consider the overall anadromous fish programs we reviewed,
examples of successes at rebuilding self-sustaining fish runs with hatchery fish are scarce.
The successes we recorded in the unpublished literature were mainly in harvest
augmentation, not rebuilding runs.

In an earlier review of supplementation, Beck (1987) makes it clear that the
supplementation strategies most often used are not necessarily related to success. Most
supplementation projects we reviewed were poorly evaluated and documented, especially
projects that were failures. Many well meaning evaluations remain in file cabinets as
raw data. Smith et al. (1985) certainly did a commendable literature review (published
and gray). We concur with his conclusions and cannot shed much new light on
supplementation. We turned over scores of gray literature stoneswithout finding any
significant new evidence that supplementation can consistently enhance natural
populations.

A few studies we reviewed demonstrated adverse impacts to wild/natural stocks from
hatchery stocking. However, when hatchery fish were released into Virgin areas; barren
lakes, above falls or barriers, in new geographic areas, directly into estuaries or coves,
they performed quite well. In these cases, managers usually were not attempting to build
a self-perpetuating run, but merely producing adult fish for augmenting harvest. When
managers attempt to introduce hatchery fish on top of an existing population to build or
rebuild the run to "historic" levels of production or to "full seeding" levels of production,
problems seem to develop. The hatchery fish do not perform as well as the wild/natural
fish and adverse impacts to the wild/natural stocks have been indicated and
demonstrated (Reisenbichler and McIntyre 1977; Chilcote et al. 1986).

Based on our review of the data and from recent interviews, we believe that hatchery
production needs to be divided into two distinct categories. These would be: (1)
hatchery production for "harvest augmentation," and (2) supplementation which is
"natural production augmentation." We believe this separation does in fact now exist but
that success has mainly been in number (1), production for harvest augmentation.

Time, effort, and knowledge needed to accomplish harvest augmentation is much less
than that needed for natural production supplementation. In order to supplement
natural production, managers need to know several factors. They need to know the
ecology of the area, the factors limiting present production, the unique qualities of the
stock of fish to be supplemented, and the most efficientmeans for supplementation. The
time frames for determining success stretches into multiple life cycles for natural
production supplementation while for harvest augmentation we can determine success in
one generation.

Fishery agencies have been stocking anadromous fish for many years in the Pacific
Northwest. There have been reports of increasing adult returns from various types of
planting strategies. Outplantings of smolts return the highest percentage of adults for
both salmon and steelhead. However, there are mixed results on the ability to rebuild or
increase natural runs by supplementing with hatchery fish. A few examples suggest that
it is possible to supplement natural runs with hatchery fish without adverse effects. For
instance - in Oregon, the Elk River run of fall chinook has been supplemented for
approximately 20 years. Although no major adverse effects have been noted from this
highly controlled supplementation program, the natural run of fall chinook did not
significantly increase either. Managers believed the Elk River wild run was at carrying
capacity prior to supplementation.

In Idaho, plants of steelhead fry in some upper Salmon River drainages is believed to
have contributed to the building up of natural spawning fish in a few of the drainages.
Streams with no apparent spawning were planted with excess fry and in subsequent years
spawning adults were noted. No numerical information is available for these
observations, and straying can not be ruled out. In BC, Coquilialla River biologists,
supplementing with hatchery fry, have documented steelhead fry-to-adult survival as high
as 1.3 percent and parr-to-adult survival of 2.6 percent for hatchery fish. After releasing
hatchery fry, a fourfold increase in standing crop of the stream was noted. Long range
build-up of natural production was not shown because of the continuous annual stocking
programs. In New England, work with Atlantic salmon demonstrates how difficult it is to
rebuild and reestablish anadromous fish runs. Stockings of fry and smolts, have both
returned adults but natural production has not really taken off.

Following are conclusions we arrived at based on our review of supplementation:

-Chinook salmon, particularly upriver stocks, are the most difficult to supplement
successfully with hatchery fish. This is because of the greater distance from the ocean
and the longer freshwater life cycle.
-The stock of fish is an important factor to consider when supplementing. The closer the
hatchery stock is to the supplemented stock or original natural stock, the better
chances are for success. Ideally, the hatchery supplementation brood fish should be
taken from the natural stock that is to be supplemented.

-Salmon species with shorter freshwater life cycle have shown a higher success rate from
hatchery supplementation. They also have less negative impacts on wild/natural
populations. Pink and chum salmon supplementation projects in Alaska and BC are
examples of this success.
-Short-run stocks of salmon and steelhead have responded more positively to
supplementation than longer-run stocks. In some cases, it was shown that introducing
hatchery stock to a river system a few kilometers closer to the estuary significantly
increased rate of adult returns.
-Wild/natural fish have higher survival rates than hatchery fish. This has been
demonstrated with pink salmon in Alaska, Atlantic salmon in Maine, coho salmon on
the coast, and upriver chinook salmon in the Columbia. Where tests were made to
compare survival to adult, wild/natural produced fish had higher survival rates than
associated hatchery produced fish.
-Overstocking of hatchery fish may be a significant problem in a lot of supplementation
projects. If hatchery fish are overstocked in a system, the result is decreased
performance of both hatchery and wild/natural fish.
-Scattering or distributing the supplemented hatchery stock is more successful than single
spot techniques which tend to overstock areas of planting and leave unplanted areas
understocked.
-There is a need to evaluate more supplementation programs. We found 18 projects that
were all or partially evaluated out of 26 projects classified as supplementation. In
order to do hatchery evaluation work or compare survival, hatchery fish need to be
identified uniquely from wild/natural stock. There is a need to have a unique visual
mark for hatchery produced chinook salmon in the Columbia River.
-Successful techniques for establishing, rebuilding, and supplementing sockeye salmon
populations have been developed in Alaska and BC. Most of these programs
integrate lake fertilization with fry plantings of appropriate stocks. Some of these
techniques may prove useful in rebuilding Columbia River sockeye populations.
-Hatchery broodstock management for supplementation needs to be stressed. The
"Summary of Recommendations Regarding Hatchery Production Principles" in draft
form, June 6, 1989, System Planning Oversight Committee, reflect many of the
concerns with hatchery broodstock management for supplementation.
-Genetic considerations should be an initial concern of all supplementation efforts aimed
at rebuilding existing runs of anadromous fish.
-Interpretation of genetic studies of hatchery/wild interaction will be difficult, and long-
term in order to obtain the necessary second and third generation data - maybe 15 to
20 years. Also, the opportunity for documenting the genetic "identity" of many native
stocks is already lost.
-Overall, conclusions from our review of supplementation show that there are many
documented cases of introduced hatchery fish returning as adults to a specific area.
However, little data were found on the capability or probability of supplemented
hatchery fish building up and sustaining wild/natural populations. Figure 1
summarizes some of the factors mentioned relative to supplementation success.

Figure 1. General success of supplementation with hatchery fish to returning adult.

Good
Success -- > --------------------- > ---------------------- > --------------------- > Poor Success
Increasing length of freshwater residency

Good
Success --> --------------------- > ----------------------> --------------------- > Poor Success
Increasing distance from ocean

Good
Success >--------------------- > ----------------------> --------------------- > Poor Success
Increasing distance between stocks used

Good
Success >--------------------- > ----------------------> --------------------- > Poor Success
Lake rearing Main river rearing Stream rearing

Introduced hatchery fish will augment the number of returning adults to a particular
area, but if the factors which originally caused the natural runs to decline are not
corrected, production will not significantly change. In fact, in some cases the presence of
additional hatchery adults can lead to increased exploitation; thus decreasing the natural
production even faster. In some studies, wild/natural stocks were shown to be more
viable than hatchery stocks. Thus, replacing wild/natural fish with hatchery fish, and
cross breeding wild/natural and hatchery fish, can result in less viable production.
(Bjorrm and Steward 1990).

If supplementation is ever going to be successful with hatchery fish, we must make major
changes in hatchery management. We must make the fish as compatible with the
environment (outplanting site) as possible. The hatchery mind-set works against fish-
environment compatibility. Changes that appear insignificant at the hatchery, e.g.,
rearing program, outplant timing, and marking etc., can seriously affect the success of
supplementation. However, when hatchery experts were questioned, 53 percent
responded that fish culture decisions are based primarily on human efficiency not
resource concerns (Diggs 1984).

Does supplementation of anadromous fish work? We believe that it can work, although
success varies dramatically by (1) species, (2) stock, (3) area, and (4) method or type of
supplementation. Also, success depends on goals we are trying to achieve. If we look at
natural production, we have very few successful examples. The two basic questions
asked in the supplementation "Proposed Five-Year Work Plan", prepared by the
Supplementation Technical Work Group (1988), are considered still quite valid. "What

are the best techniques for supplementing wild/natural stocks and what are the effects of
supplementation on endemic populations?" We consider the information presented in
Smith et al. (1985) in their "Outplanting Anadromous Salmonids - A Literature Survey"
to be very pertinent. The survey does in fact contain representative information we have
found to be substantiated in our own literature work and interviews.

We concur with Smith et al. (1985) that no supplementation procedures should be
attempted in wild/natural fish only streams. These streams are best enhanced by habitat
protection and harvest control.

We believe that plans to double anadromous fish runs in the Columbia River Basin, as
stated in the Northwest Power Planning and Conservation Act, may be placing too much
emphasis on hatchery production. This effort may continue to erode -the genetic integrity
of wild stock. We believe that the only way to "double the runs" in the Columbia Basin
is to provide optimum habitat for natural producing stocks with limited hatchery
supplementation. Equally important is the need to improve mainstream passage
conditions by providing adequate flows and reducing losses at the dams. In addition,
some hatchery programs should probably divert their efforts at "harvest augmentation"
with no or minimal impacts to natural production. If hatchery production, as we know it
today, could solve the production problem in the Columbia Basin, we would have
doubled the runs 50 years ago.

We may have created an "environmental predicament" where "man's ability to modify the
environment increases faster than his ability to foresee the effects of his activities" (Bella
and Overton 1972). We must make every effort to reduce the genetic consequences of
large scale outplanting. We believe that in many instances anadromous fish could do a
better job of rebuilding if we would place a moratorium on "helping" them for several
generations. We need to refocus our efforts to protect and enhance habitat. We have
tried for 100 years "to have our cake and eat it too," the time is ripe for more innovative
methods of hatchery outplanting.

Again, we may need to look at what factors caused the runs to decr *ease in the first
place. If we have not ameliorated the problems which caused the runs to decrease, we
will not be able to build up natural runs by just planting hatchery fish. Also, if harvest
management is not linked with supplementation, the increased harvest on supplemented
fish may in fact put increased harvest pressure on natural stocks. Thus, the overall result
would be a negative impact to natural production.

RECOMMENDATIONS

1. A means needs to be established for annually summarizing and updating
supplementation efforts by geographic area. Many supplementation projects are
underway or planned throughout the northwest. Since supplementation projects
normally span a number of years, it is important to update our information base
annually. A state-by-state annual summary based on the format of the New England
Atlantic salmon program annual reports is suggested.

2. A means of identifying hatchery salmon from wild/natural salmon needs to be
instituted for the Columbia River Basin. A visual mark is needed so hatchery and
wild/natural escapement and production can be monitored and runs manage
separately.

3. Factors related to hatchery fish survival need to be studied. Hatchery spring chinook
salmon were found to be the least successful species to supplement. We believe from
our discussion with workers in the Basin that BKD is a major factor contributing to
this poor success. Therefore, BKD research on spring chinook salmon should be a
high priority.

Recommended Research

1. Assessment of factors limiting wild/natural production by area and species in
association with carrying capacity.

2. Impact of hatchery smolt releases on wild/na tural smolt production and migration.

3. Develop a hatchery rearing broodstock program for stock rebuilding that minimizes
adverse genetic impacts to wild/natural stocks. Explore use of wild/natural stocks.
Sperm cryopreservation and other innovations could be used to direct hatchery
production to a more compatible product. Using kelts for wild steelhead production
could be investigated.

4. Need to determine natural production parameters for stocks to be supplemented.

5. Need to develop a means of identifying hatchery from wild/natural fish for salmon in
Columbia River Basin.

6. Need to explore use of strearnside upwelling incubation boxes or systems to match
natural production timing.

LITERATURE CITED

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95. In: M.A. Miller. Southeast Alaska coho salmon research and management
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Game Report.

Anonymous. 1982a. Comprehensive plan for production and management of Oregon's
anadromous salmon and trout: Part 1. General considerations. Oregon Department
of Fish and Wildlife.

Anonymous. 1982b. Comprehensive plan for production and management of Oregon's
anadromous salmon and trout: Part 11. Coho salmon plan. Oregon Department of
Fish and Wildlife.

Anonymous. 1985. Fisheries 1986-1990 management plan. Idaho Department of Fish
and Game. Draft.

Anonymous. 1987a. Supplementation overview - does it work? Washington
Department of Fisheries.

Anonymous. 1987b. The New England Atlantic salmon program annual progress report.
U.S. Fish and Wildlife Service. Region 5.

Anonymous. 1988. The New England Atlantic salmon program annual progress report.
U.S. Fish and Wildlife Service. Region 5.

Anonymous. 1989a. Annual fish passage report - 1988. North Pacific Division Corps of
Engineers, Portland, Oregon.

Anonymous. 1989b. Salmonid enhancement program 1989 update. Department of
Fisheries and Oceans, Vancouver BC.

Anonymous. 1990a. Natural production and wild fish management rules. Oregon
Department of Fish and Wildlife.

Anonymous. 1990b. 1989 annual report of the U.S. Atlantic salmon assessment
committee. U.S. Atlantic Salmon Assessment Committee.

Beck, R.W. 1987. Review of hatchery supplementation methods and effects. Appendix
IV in Yakima and Klickitat River central outplanting facility proposed master plan.
Report to Northwest Power Planning Council, Portland, Oregon.

Bell a, D.A-, and W.S. Overton. 1972. Environmental planning and ecological
possibilities. Proceedings of the American Society of Civil Engineers. 98(SA3):
579-592.

Bjornn, T.C., and C.R. Steward. 1990. Concepts for a model to evaluate
supplementation of natural salmon and steelhead stocks with hatchery fish. U.S.
Department of Energy, Bonneville Power Administration Project 88-100.

Boyle, L., and N. Dudiak. 1986. Tutka Lagoon Hatchery 1981 adult return evaluation.
Alaska Department of Fish and Game, FRED Division, No. 61.

Chilcote, M.W., S.A. Leider, and J.J. Loch. 1986. Differential reproductive success of
hatchery and wild summer-run steelhead under natural conditions. Transactions of
the American Fisheries Society 115:726-735.

Diggs, D.H. 1984. A "Delphi" survey into the methods and practices of spring chinook
salmon culture. U.S. Fish and Wildlife Service, Dworshak Fisheries Assistance
Office, Ahsahka, Idaho.

Dudiak, N., and L. Boyle. 1988. Homer area sport fisheries enhancement. Alaska
Department of Fish and Game, FRED Division, Vol. 3, No. 6.

Fast, D.E., J.D. Hubble, and M.S. Kohn. 1988. Yakima River spring chinook
enhancement study. 1988 Annual Report to Bonneville Power Administration,
Contract No. 82-16.

Fulton, L. A. 1968. Spawning area and abundance of chinook salmon (Oncorhynchus
tshavqtscha) in the Columbia River Basin--past and present. U.S. Fish and Wildlife
Service Scientific Report, Fisheries No. 571.

Gerstung, E.R. 1981. Status and management of the coast cutthroat trout, Salmo clarki
clarki. Cal-Nev Wildlife transactions.

Gibson, M.R. 1989. Atlantic salmon restoration studies January 1, 1988 to December
31, 1988. Performance Report. Job No. 111-4. Rhode Island Division of Fish and
Wildlife.

Hartman, J.L., J.S. Holland, Jr., M. Kaill, and J.L. Madden. 1988. Enhancement and
rehabilitation, a successful investment in Alaska's fisheries. In: Alaska Fish and
Game 21:4-8.

Herrig, D.M. 1990. Lower Snake River Compensation Plan - A review of the
compensation program (Draft). U.S. Fish and Wildlife Service, Lower Snake River
Compensation Plan Office, Boise, Idaho.

Hillman, T.W., and J.W.'Mullan. 1989. Effect of hatchery releases on the abundance
and behavior of wild juvenile salmonids in a large Washington river. Submitted to
North American Journal of Fisheries Management.

Holland, J.S. 1989. FRED 1988 annual report to the Alaska State Legislature. Alaska
Department of Fish and Game, FRED Division, Juneau, Alaska.

Hurst, R.E., and B.G. Blackman. 1988. Coho Colonization Program: Juvenile studies
1984 to 1986. Canadian Manuscript Report of Fisheries and Aquatic Sciences No.
1968.

Johnson, S.L. 1982. A review and evaluation of release strategies for hatchery reared
coho salmon. Oregon Department of Fish and Wildlife Information Reports (Fish)
82-5, Portland, Oregon.

Kohler, T. 1984. Pink and chum salmon adult returns from releases at Cannery Creek
and Main Bay Hatcheries: 1983 field season. Alaska Department of Fish and Game,
FRED Division, No. 34.

Koski, C.H., S.W. Pettit, and J.L. McKern. 1990. Fish transportation oversight team
annual report - FY 1989. Transport operations on the Snake and Columbia Rivers.
NOAA Technical Memorandum NMFSF/NWR-27.

Kyle, G.B., and D.S. Litchfield. 1989. Enhancement of Crooked River chinook salmon
(Oncorhynchus tshauytscha) and development of a sport fishery on the Kasilof River.
Alaska Department of Fish and Game, FRED Division, No. 97.

Leider, S.A., J.J. Loch, and P.L. Hulett. 1989. Studies of hatchery and wild steelhead in
the lower Columbia region. 1989 Progress Report. Washington Department of
Wildlife. Report 89-5.

Litchfield, D.S., and L.B. Flagg. 1988. Hidden Lake sockeye salmon investigations,
1983-1984. Alaska Department of Fish and Game, FRED Division, No. 86.

McDaniel, T.R., T. Kohler, and D.M. Dougherty. 1984. Results of pink salmon
(Oncorhynchus gorbuscha) fry transplants to Holo Creek, Prince William Sound,
Alaska. Alaska Department of Fish and Game, FREEi Division, No. 33.

Minta, P., S. Gephard, and R. VanNostrand. 1987. Anadromous fish enhancement
restoration. 1987 Annual Performance Report, F-50-D-8. CT DEP/Marine
Fisheries, Waterford, CT.

Nicholas, J.W., and T.W. Downey. 1989. Looking Back on tow decades of work at Elk
River Hatchery: Has there been harmony between the natural and artificial
production systems? And has Elk River been a prototype conservation hatchery.
(First Draft). Oregon Department of Fish and Wildlife.

Nicholas, J.W., and D.G. Hankin. 1989. Chinook salmon populations in Oregon coastal
river basins. Oregon Department of Fish and Wildlife Information Report 88-1,
Portland, Oregon.

Nickelson, T.E. 1981. Coho pre-smolt program for Oregon coastal streams. Oregon
Department of Fish and Wildlife Information Report (Fish) 81-1, Portland, Oregon.

Ptolemy, R.A. 1986. , Assessment of highway construction impacts and fisheries
mitigation in the Coquihalla River near Hope, British Columbia: progress in 1985.
BC Fisheries Project Report No. FIU-04.

Raymond, H.L. 1988. Effects of hydroelectric development and fisheries enhancement
on'spring and summer chinook salmon and steelhead in the Columbia River Basin.
North American Journal of Fisheries Management 8:1-24.

Raymond, J.A. 1986. Growth of wild and hatchery juvenile coho salmon in an interior
Alaska stream. Alaska Department of Fish and Game, FRED Division. No. 60.

Reisenbichler, R.R., and J.D. McIntyre. 1977. Genetic differences in growth and
survival of juvenile hatchery and wild steelhead trout, Salmo gairdnefi. Journal
Fisheries Research Board of Canada 34:123-128.

Smith, E.M. 1987. Outplanting experience in Oregon. Oregon Department of Fish and
Wildlife.

Smith, E.M., B.A. Miller, J.D. Rodgers, and M.A. Buckman. 1985. Outplanting
anadromous salmonids - a literature survey. U.S. Department of Energy, Bonneville
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hatchery coho pre-smolts to increase the rearing density of juvenile coho salmon in
Oregon coastal streams. Oregon Department of Fish and Wildlife, Information
Report 83-4, Portland, Oregon.

Steward, C.R., and T.C. Bjornn. 1990. Supplementation of salmon and steelhead stocks
with hatchery fish: A Synthesis of published literature. U.S. Department of Energy,
Bonneville Power Administration Project 88-100.

Supplementation Technical Work Group. 1988. Supplementation research - proposed
five-year work plan. Unpublished document.

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Alaska 1978-1984. Alaska Department of Fish and Game, FRED Division, No. 69.

APPENDIX A

PART I

Table of the 26 projects considered true supplementation (for codes used in data
entry and reporting see Part 3 of Appendix A).

SUPPLEMENTATION REPORT

LIFE MAJOR SUB PRINCIPAL #/YEAR
SPECIES RACE STOCK STAGE DRAINAGE DRAINAGE EVAL AGENCY CONTACT PHONE RELEASED PURPOSE OF PROJECT

6. AS MIXED SM,FY,PR Mc ON FWS JERRY MARANCIK (207)469-6701 1900000 SUPPLEMENTATION, RESTORATION
7. AS MIXED SM,FY,PR Mc ON MSRSC ED BAUM (207)941-4452 1900000 SUPPLEMENTATION, RESTORATION
10. CH AD BC ON ABREC J. FEE 2150 SUPPLEMENTATION EVALUATION STUDY
11. CH FY BC ON CFSO GORDON BEREZAY (604)666-2600 125000 SUPPLEMENTATION
14. CH BR FY,SM BC ON CFSO GORDON BEREZAY (604)666-2600 107344 SUPPLEMENTATION, ENHANCE RUNS
26. CH MT PS,FN cc 18010108 ON MWSSG GARY PETERSON (707)629-3514 30000 SUPPLEMENTATION, ENHANCE WILD STOCKS
36. CH FAL CH EG,FY,SM OC 17100306 ON ODFW JAY NICHOLAS (503)737-4431 400000 SUPPLEMENTATION, ENHANCE RUNS
50. CH FAL HR YR cc 18010112 ON PCFFA MITCH FARRO (707)839-5664 30000 SUPPLEMENTATION, ENHANCE RUNS
52. CH FAL LR SM cc 18010108 ON PCFFA MITCH FARRO (707)839-5664 50000 SUPPLEMENTATION, ENHANCE RUNS
73. CH SPR FN,SM CR FWS BILL MILLER (208)476-7242 200000 SUPPLEMENTATION, ENHANCE RUNS
94. CH SUM ST FN PS 17110008 OA STIL KIP KILLEBREW (206)435-8770 81093 SUPPLEMENTATION, ENHANCE RUNS
120. CO FY BC ON CFSO ROBERT HURST (604)756-7296 9500 SUPPLEMENTATION, STOCK EVALUATION
161. CO MT YR,SM cc 18010108 ON MWSSG GARY PETERSON (707)629-3514 8000 SUPPLEMENTATION, ENHANCE WILD STOCKS
180. CO TM Ps'sm Oc 17100304 ON ODFW PAUL REIMERS (503)888-5515 180000 SUPPLEMENTATION, ENHANCE WILD STOCKS
182. CO TR FY BC ON CFSO ROBERT HURST (604)756-7296 7500 SUPPLEMENTATION
210. CU SEA RW YR cc 18010102 OA HBCO STEVE SANDERS (707)488-2253 500 SUPPLEMENTATION, ENHANCE WILD STOCKS
219. SH FY BC ON MEBC JEREMY HUME (604)660-1812 0 SUPPLEMENTATION
234. SH KR SM ac ON MEBC BRUCE WARD (604)660-1812 20000 SUPPLEMENTATION
238. SH NP YR cc .18050002 ON NRS GEORGE CARL (707)252-1440 7000 SUPPLEMENTATION, ENHANCE RUNS
248. SH YK,SK,RI,PR SM,FY CR 17030002 QA WDW JIM CUMMINS (509)575-2740 0 SUPPLEMENTATION, ENHANCE WILD STOCKS
251. SH SUM AD,FY,SM CR QA FWS BILL MILLER (208)476-7242 1000000 SUPPLEMENTATION, ENHANCE RUNS
256. SH SUM NR FY BC ON MEBC BRAIN BLACKMAN (604)565-6413 23550 SUPPLEMENTATION, ENHANCE PRODUCTION
257. SH SUM sc FY Bc ON BOB GRIFFITH (604)387-3660 11400 SUPPLEMENTATION
288. SH WIN CH,BG SM,FY WC 17100101 ON WDW BILL FREYMOND (206)533-9335 171711 SUPPLEMENTATION, ENHANCE WILD STOCKS
312. SO FN AC ON ADFG DAVID LITCHFIELD (907)262-9369 1400000 SUPPLEMENTATION, ENHANCE RUN
313. So EG AC ON ADFG LORNE WHITE (907)486-4791 6000000 SUPPLEMENTATION, ENHANCE NATURAL RUN

APPENDIX A

PART 2

Summary of the 26 projects considered true supplementation (for codes used in
data entry and reporting see Part 3 of Appendix A).

6. SPECIES: AS RACE: STOCK(S): MIXED
MAJOR DRAINAGE: MC SUB DRAINAGE: 15 RIVERS IN MAINE
CONTACT: JERRY MARANCIK PHONE: (207)469-6701
AGENCY: FWS ADDRESS: GRAIG BROOK NFH, E. ORLAND, ME 04431
PROJECT: MAINE ATLANTIC SALMON PROGRAM
PURPOSE: SUPPLEMENTATION, RESTORATION ONGOING: Y
EVALUATION: QN : 26,790 FISH HAVE RETURNED TO MAINE RIVERS
SURVIVAL: SEE PROJECT # 7
STOCKING DETAILS:
ACCLIMATION DETAILS:
OTHER PRE STOCKING INFO:
IMPACTS; RESEARCH: 10% OF RETURNS TO THE PENOBSCOT R. IS FROM NATURAL PRODUCTION
IMPACTS; OPINION:
CONTROL DETAILS:
OTHER COMMENTS: 2,141 OUT OF 2,688 FISH (IN 1988) ALLOWED TO SPAWN NATURALLY

7. SPECIES: AS RACE: STOCK(S): MIXED
MAJOR DRAINAGE: MC SUB DRAINAGE: 15 RIVERS IN MAINE
CONTACT: ED BAUM PHONE: (207)941-4452
AGENCY: MSRSC ADDRESS: P.O. BOX 1298, BANGOR, ME 04401
PROJECT: MAINE ATLANTIC SALMON PROGRAM
PURPOSE: SUPPLEMENTATION, RESTORATION ONGOING: Y
EVALUATION: QN :
SURVIVAL: ADULT RETURNS RANGE FROM .23 TO 1.32%, MEAN = .71%
STOCKING DETAILS: MAINLY SMOLT STOCKING
ACCLIMATION DETAILS:
OTHER PRE STOCKING INFO: 47% OF RELEASES TO THE PENOBSCOT RIVER
IMPACTS; RESEARCH: FISH UNNEEDED FOR EGG TAKES ARE ALLOWED TO SPAWN NATURALLY
IMPACTS; OPINION: RETURNS TO "WILD" RIVERS ARE PRIMARILT OF WILD ORIGIN
CONTROL DETAILS:
OTHER COMMENTS: MAINE PRODUCED ALL OF THE SPORT CATCH IN 1989, 86% OF THAT FROM THE
PENOBSCOT RIVER

10. SPECIES: CH RACE: STOCK(S):
MAJOR DRAINAGE: BC SUB DRAINAGE: SHUSWAP RIVER
CONTACT: J. FEE PHONE:
AGENCY: ABREC ADDRESS: VICTORIA, B.C.
PROJECT: EVALUATION OF CHINOOK & COHO OUTPLANTING OPPORTINUITY, SHUSWAP RIVER
PURPOSE: SUPPLEMENTATION EVALUATION STUDY ONGOING: N
EVALUATION: QN : POSSIBLE RETURN OF 240-430 FISH
SURVIVAL: PRE-SUPPLEMENTATION WORK (SEE COMMENTS
STOCKING DETAILS: NEED TO STOCK TO DENSITIES OF @.O AND 6.0 G/SQ. METER
ACCLIMATION DETAILS:
OTHER PRE STOCKING INFO: WOULD FULLY SEED USUABLE REARING HABITATS
IMPACTS; RESEARCH:
IMPACTS; OPINION:
CONTROL DETAILS:
OTHER COMMENTS: BC DOES RECONNAISSANCE REPORTS ON ALL STREAMS BEFORE SUPPLEMENTATION
TO DETERMINE OPPORTUNITIES FOR RESTORATION & ENHANCEMENT OF ENDIMICS

ii. SPECIES: CH RACE: STOCK(S):
MAJOR DRAINAGE: BC SUB DRAINAGE: UPPER FRASER RIVER
CONTACT: GORDON BEREZAY PHONE: (604)666-2600
AGENCY: CFSO ADDRESS: 555 W HASTINGS ST., VANCOUVER, BC V6B 5G3
PROJECT: PENNY CHINOOK PILOT HATCHERY, OPERATIONAL HISTORY, 1980-83
PURPOSE: SUPPLEMENTATION ONGOING: Y
EVALUATION: QN :
SURVIVAL: EGGS TO FRY = 74-90%, FRY TO ADULT = 0 -.10%
STOCKING DETAILS: VIA HELICOPTER IN OXYGENATED 360 LITER TANKS
ACCLIMATION DETAILS: BROODSTOCK COLL. FROM & FRY TRANSPORTED TO NATAL STREAMS
OTHER PRE STOCKING INFO: FRY TAGGED @ 1-2 G
IMPACTS; RESEARCH: LOW SUR. TO ADULT INDICATES THE PROD. STRATEGY SHOULD BE REASSESSED
IMPACTS; OPINION: MODIFY PROGRAM TO INCREASE POST-RELEASE SURVIVAL
CONTROL DETAILS:
OTHER COMMENTS: OPERATION RESULTED IN SUCCESSFUL REARING OF CHINOOK FRY IN COLD
WATER 1-5 oC

A2-1

14. SPECIES: CH RACE: STOCK(S): BR
MAJOR DRAINAGE: BC SUB DRAINAGE: HARRISONRIVER
CONTACT: GORDON BEREZAY PHONE: (604)666-2600
AGENCY: CFSO ADDRESS: 555 W. HASTINGS ST., VANCOUVER, BC V6B 5G3
PROJECT: BIRKENHEAD RIVER CHINOOK HATCHERY OPERATIONAL HISTORY 1977-86
PURPOSE: SUPPLEMENTATION, ENHANCE RUNS ONGOING: Y
EVALUATION: QN : LOW RETURNS INDICATE VERY POOR MARINE SURVIVAL
SURVIVAL: LOW TAG RETURNS FOR 77-81 BROODS 0-0.3%
STOCKING DETAILS: FRY RELEASED 2-4G BY 1984 AND 5-7G LATER
ACCLIMATION DETAILS:
OTHER PRE STOCKING INFO:
IMPACTS; RESEARCH: BIRKENHEAD HATCHERY UNABLE TO MEET GOALS DUE TO LOW ESCAPEMENT
IMPACTS; OPINION: PROBLEM AGGRAVATED BY HIGH EXPLOTATION RATE IN INDIAN FISHERY
CONTROL DETAILS: LOW TAG RETURNS MAY BE RESULT OF INSUFICIENT TAGGED FISH
OTHER COMMENTS: LIMITED COHO & STEELHEAD PRODUCTION

26. SPECIES: CH RACE: STOCK(S): MT
MAJOR DRAINAGE: CC SUB DRAINAGE: MATTOLE RIVER
CONTACT@ GARY PETERSON .PHONE: (707)629-3514
AGENCY: MWSSG ADDRESS: P.O.BOX 188, PETROLIA, CA 95538
PROJECT: MATTOLE WATERSHED SAI14ON SUPPORT CROUP
PURPOSE: SUPPLEMENTATION, ENHANCE WILD STOCKS ONGOING: Y
EVALUATION: QN : CWT PROGRAM(2 YEARS);JUVENILE TRAPPING; SPAWNING SURVEYS
SURVIVAL: POPULATIONS STATIC
STOCKING DETAILS: DUSK OR EVENING RELEASE WITH NEW MOON PHASE
ACCLIMATION DETAILS: TEMPERATURE ACCLIMATION
OTHER PRE STOCKING INFO: FISH TAKEN OFF FEED AND SALTED PRIOR TO STOCKING
IMPACTS; RESEARCH:
IMPACTS; OPINION: POPULATIONS ARE STATIC- NO INCREASE OR DECREASE
CONTROL DETAILS:
OTHER COMMENTS: STOCKS MAY BE STATIC DUE TO JUVENILE BOTTLENECK IN ESTUARY

36. SPECIES: CH RACE: FAL STOCK(S): CH
MAJOR DRAINAGE: OC SUB DRAINAGE: ELK RIVER CHETCO RIVER
CONTACT: JAY NICHOLAS PHONE: (503)737-4431
AGENCY: ODFW ADDRESS: 28655 HWY 34, CORVALLIS, OR 97330
PROJECT: ELK RIVER STUDY
PURPOSE: SUPPLEMENTATION, ENHANCE RUNS ONGOING: Y
EVALUATION: QN : EST. SURVIVAL RATE DOES NOT INCLUDE OCEAN CATCH
SURVIVAL: MEAN ADULT = 2.42% RETURN TO ELK RIVER (MOUTH) (68-78 BROOD)
STOCKING DETAILS: TRUCK SMOLTS AND FRY, USE HATCH BOXES
ACCLIMATION DETAILS:
OTHER PRE STOCKING INFO: PRE HATCHERY EVALUATION WAS COMPLETED
IMPACTS; RESEARCH: BROODSTOCK SEINED FROM CHETCO R., 25,000 CWT STOCK ASSESSMENT
IMPACTS; OPINION: FEEL THAT IT STABALIZES RUN
CONTROL DETAILS: N@A
OTHER COMMENTS: PU LIC HAS INFLUENCED ALLOCATION INCREASES TO THE CHETCO, AS WELL AS
INCREASES IN MARKING AND EVALUATION

50. SPECIES: CH RACE: FAL STOCK(S): HR
MAJOR DRAINAGE: CC SUB DRAINAGE: TRINITY RIVER
CONTACT: MITCH FARRO PHONE: (707)839-5664
AGENCY: PCFFA ADDRESS: 216 H ST., EUREKA, CA 95501
PROJECT: KLAMATH-TRINITY FALL CHINOOK ENHANCEMENT PROJECT
PURPOSE: SUPPLEMENTATION ENHANCE RUNS ONGOING: Y
EVALUATION: QN : USDI SPAWNING SURVEYS SINCE 1981; CWT PROGRAM
SURVIVAL: N/A
STOCKING DETAILS: FISH NOT HANDLED DURING RELEASE; RELEASED AFTER 1ST STORMS
ACCLIMATION DETAILS:
OTHER PRE STOCKING INFO: FOREST SERVICE HAS ESTIMATED CARRYING CAPACITY
IMPACTS; RESEARCH: MARK RETURNS INDICATE PROGRAM IS SUCCESSFUL
IMPACTS; OPINION:
CONTROL DETAILS:
OTHER COMMENTS:

A2-2

52. SPECIES: CH RACE: FAL STOCK(S): IR
MAJOR DRAINAGE: CC SUB DRAINAGE: LITTLE RIVER
CONTACT: MITCH FARRO PHONE: (707)839-56,64
AGENCY: PCFFA ADDRESS: P.O.BOX 291, TRINIDAD, CA 95570
PROJECT: LITTLE RIVER FALL CHINOOK ENHANCEMENT PROGRAM
PURPOSE: SUPPLEMENTATION, ENHANCE RUNS ONGOING: Y
EVALUATION: QN : CWT PROGRAM; SPAWNING GROUND SURVEYS SINCE 1985
SURVIVAL: NIA
STOCKING DETAILS: 100% CWT; TRUCKED; LATE EVENING RELEASES WITH LUNAR PHASE
ACCLIMATION DETAILS: TEMPERATURE ACCLIMATION
OTHER PRE STOCKING INFO:
IMPACTS; RESEARCH: FIRST RETURNS CAME IN 1988,SHOWS PROJECT HAS CONTRIBUTED TO RUNS
IMPACTS; OPINION:
CONTROL DETAILS: SPLIT RELEASE STRATEGY (LOWER VS. UPPER RIVER)
OTHER COMMENTS: LAND USE PRACTICES CAN IMPACT PROJECT; ADULT MALES USED ONLY
ONCE; ONLY MARKED FISH ARE SPAWNED

73. SPECIES: CH RACE: SPR STOCK(S):
MAJOR DRAINAGE: CR SUB DRAINAGE: LOCHSA RIVER
CONTACT: BILL MILLER PHONE: (208)476-7242
AGENCY: FWS ADDRESS: P.O. BOX 18, AHSAHKA, ID 83520
PROJECT: UPPER LOCHSA ON THE CLEARWATER RIVER
PURPOSE: SUPPLEMENTATION, ENHANCE RUNS ONGOING: Y
EVALUATION: : STATE RUN WIER FIRST OPERATED IN 1989, NO PAST EVALUATION
SURVIVAL: IDAHO DEPT. OF FISH & GAME OPERATES WIER
STOCKING DETAILS: TRUCKED FROM DWORSHAK NFH TO POWELL & RELEASED
ACCLIMATION DETAILS: RAISED ON NF CLEARWATER R., CURRENTLY RAISED AT POWELL
OTHER PRE STOCKING INFO: CHINOOK CWTed IN 1989, 60,000 OUT OF 200,000 RELEASED
IMPACTS; RESEARCH:
IMPACTS; OPINION:-
CONTROL DETAILS:
OTHER COMMENTS: MAY HAVE HAD 1 OCEAN RETURNS IN 1989 BUT WEIR WAS NOT OPERATED DUE
TO CONSTRUCTION

94. SPECIES: CH RACE: SUM STOCK(S): ST
MAJOR DRAINAGE: PS SUB DRAINAGE: STILLAGUAMISH RIVER
CONTACT! KIP KILLEBREW PHONE: (206)435-8770
AGENCY: STIL ADDRESS: 3439 STOLUCKQUAMISH LN, ARLINGTON, WA 98223
PROJECT: STILIAGUAMISH CHINOOK
PURPOSE: SUPPLEMENTATION, ENHANCE RUNS ONGOING: Y
EVALUATION: QA : SPAWNING SURVEYS DONE ANNUALLY
SURVIVAL: RELATIVE SURVIVAL RATES TO BE EVALUATED
STOCKING DETAILS: DUMP PLANTED INTO MAINSTEM & MOUTHS OF TRIBS
ACCLIMATION DETAILS: 41,115 FN AT FORTSON POND FOR 16 DAYS AVG. IN 89
OTHER PRE STOCKING INFO: TRY TO MATCH PLANTINGS TO TIME & SIZE OF WILD OUTMIGR
IMPACTS; RESEARCH:
IMPACTS; OPINION: ANY INCREASE IS A BENEFIT, RUN IS SLOWLY INCREASING
CONTROL DETAILS: 405,998 FISH TAGGED WITH CWT
OTHER COMMENTS: ADDL. STREAMS: ARMSTRONG,HARVEY,CANYON,BEAVER,PERRY,& PALMER

120. SPECIES: CO RACE: STOCK(S):
MAJOR DRAINAGE: BC SUB DRAINAGE: CRAIG CREEK
CONTACT: ROBERT HURST PHONE: (604)756-7296
AGENCY: CFSO ADDRESS: 3225 STEPHENSON PT RD, NANAIMO, BC V9T 4P7
PROJECT: CRAIG CREEK
PURPOSE: SUPPLEMENTATION, STOCK EVALUATION ONGOING: Y
EVALUATION: QN : WILD BROODSTOCK COLLECTED FROM CRAIG CK & REARED IN HATCHERY
SURVIVAL: WILD=4.2%, HATCHERY=3.2%
STOCKING DETAILS: STOCKS DIFFERENTLY MARKED & RELEASED INTO CRAIG CK HEADWATER
ACCLI14ATION DETAILS:
OTHER PRE STOCKING INFO: WILD FRY .2 C LARGER THAN HATCHERY FRY
IMPACTS; RESEARCH: SURVIVAL OF WILD FISH SIG HIGHER THAN HATCHERY
IMPACTS; OPINION: STOCKING DENSITIES WERE EXCESSIVE, RESULTING IN LOW SURVIVAL
CONTROL DETAILS:
OTHER COMMENTS: OBJECTIVES: (1)DETERMINE DECLINE IN FRY TO SMOLT SURVIVAL RATE
(2)PROVIDE ADDITIONAL INFO ON OPTIMUM STOCKING DENSITIES FOR COHO

A2-3

161. SPECIES: CO RACE: STOCK(S): MT
MAJOR DRAINAGE: CC SUB DRAINAGE: MATTOLE RIVER
CONTACT: GARY PETERSON PHONE: (707)629-3514
AGENCY: MWSSG ADDRESS: P.O.BOX 188, PETROLIA, CA 95538
PROJECT: MATTOLE WATERSHED SALMON SUPPORT GROUP
PURPOSE: SUPPLEMENTATION, ENHANCE WILD STOCKS ONGOING: Y
EVALUATION: QN : CWT PROGRAM(2 YEARS); JUVENILE TRAPPING; SPAWNING SURVEYS
SURVIVAL: POPULATIONS STATIC
STOCKING DETAILS: DUSK OR EVENING RELEASES WITH NEW MOON PHASE
ACCLIMATION DETAILS: TEMPERATURE ACCLIMATION
OTHER PRE STOCKING INFO: FISH TAKEN OFF FEED AND SALTED PRIOR TO STOCKING
IMPACTS; RESEARCH:
IMPACTS; OPINION: POPULATIONS ARE STATIC- NO INCREASE OR DECREASE
CONTROL DETAILS:
OTHER COMMENTS: PROJECT HAS ESTABLISHED RUNS IN DIFFERENT TRIBUTARIES

180. SPECIES: CO RACE: STOCK(S): TM
MAJOR DRAINAGE: OC SUB DRAINAGE: EEL LAKE
CONTACT: PAUL REIMERS PHONE: (503)888-5515
AGENCY: ODFW ADDRESS: P.O.BOX 5430, CHARLESTON, OR 97420
PROJECT: EEL LAKE COHO STUDIES
PURPOSE: SUPPLEMENTATION, ENHANCE WILD STOCKS ONGOING: Y
EVALUATION: N : CWT PROGRAM; SURVIVAL BASED ON CONTRIBUTION AND RETURNING ADULTS
SURVIVAL: 1.?7% TO ADULTS
STOCKING DETAILS: STOCK AFTER THE BASS ACTIVITY SLOWS DOWN
ACCLIMATION DETAILS:
OTHER PRE STOCKING INFO:
IMPACTS; RESEARCH: FISH GET PHENOMENAL GROWTH WHEN REARED IN THE LAKE
IMPACTS; OPINION:
CONTROL DETAILS:
OTHER COMMENTS: THIS PROGRAM UTILIZES EEL LAKE AS A REARING AREA; WILD FISH
ARE CONTINUALLY FUSED INTO THIS PROGRAM TO MAINTAIN THE GENETICS

182. SPECIES: CO RACE: STOCK(S): TR
MAJOR DRAINAGE: BC SUB DRAINAGE: TRENT RIVER, CANADA
CONTACT: ROBERT HURST PHONE: (604)756-729b
AGENCY: CFSO ADDRESS: 3225 STEPHENSON PT RD, NAMAIMO, BC V9T 4P7
PROJECT: TRENT RIVER - COLONIZATION
PURPOSE: SUPPLEMENTATION ONGOING: Y
EVALUATION: QN : DOWN STREAM SMOLT TRAP ON BRADLEY LK,
SURVIVAL: BRADLEY LK, FRY TO SMOLT=19%, OUTPLANTED FRY IN TRENT R-5.4%
STOCKING DETAILS: STOCKED FORM 81-86 ONLY EVALUATED IN 86
ACCLIMATION DETAILS: N/A
OTHER PRE STOCKING INFO:
IMPACTS; RESEARCH: BRADLEY L HAS GOOD SMOLT PROD. POTENTIAL & PRODUCED LARGER SMOLTS
IMPACTS; OPINION: 2-2.5 G COHO FRY DO WELL IN LAKES W1 FEW PREDATORS & LOW GRADIENT STS
CONTROL DETAILS: N/A
OTHER COMMENTS:

210. SPECIES: CU RACE: SEA STOCK(S): RW
MAJOR DRAINAGE: CC SUB DRAINAGE: REDWOOD CREEK
CONTACT: STEVE SANDERS PHONE: (707)488-2253
AGENCY: HBCO ADDRESS: PRARIE CREEK FISH HATCHERY, ORICK, CA 95555
PROJECT: PRARIE CREEK FISH HATCHERY
PURPOSE: SUPPLEMENTATION, ENHANCE WILD STOCKS ONGOING: Y
EVALUATION: QA :
SURVIVAL: INCREASE IN CUTTHROATS IN LOST MAN CREEK
STOCKING DETAILS: RELEASE WITH NEW MOON PHASE
ACCLIMATION DETAILS:
OTHER PRE STOCKING INFO:
IMPACTS; RESEARCH:
IMPACTS; OPINION: INCREASE IN ABUNDANCE OF COASTAL CUTTHROAT IN LOST MAN CREEK
CONTROL DETAILS:
OTHER COMMENTS:

A2-4

219. SPECIES: SH RACE: STOCK(S):
MAJOR DRAINAGE: BC SUB DRAINAGE: VANCOUVER,,ISLAND & MAINLAND
CONTACT: JEREMY HUME PHONE: (604)660-1 2
AGENCY: MEBC ADDRESS: 2204 MAIN MALL, UNIV. OF B.C., VANCOUVER, B.C. V6T 1W5
PROJECT: EFFECTS OF VAR. STOCKING STRATEGIES & GROWTH OF HEADWATER STOCKED SH
PURPOSE: SUPPLEMENTATION ONGOING: N
EVALUATION: QN :
SURVIVAL: SURVIVAL TO 2+ SMOLTS WAS HIGHER FOR LATER REL & LARGER FRY
STOCKING DETAILS: STOCK ABOUT 0.1 FRY/SQ METER
ACCLIMATION DETAILS:
OTHER PRE STOCKING INFO: ABOVE 0.7 FRY/SQ M. THERE WILL BE NO INCREASE IN PROD.
IMPACTS; RESEARCH: FRY FROM HIGH DENSITY GROUPS SMALLER THAN THOSE IN LOW, MED GROUPS
IMPACTS; OPINION:
CONTROL DETAILS:
OTHER COMMENTS: ASSUME WILD/NATURAL BROODSTOCK

234. SPECIES: SH RACE: STOCK(S): KR
MAJOR DRAINAGE: BC SUB DRAINAGE: KEOUGH RIVER
CONTACT: BRUCE WARD PHONE: (604)660-1812
AGENCY: MEBC ADDRESS: 2204 MAIN MALL, UNIV. OF B.C., VANCOUVER, BC V6T 1W5
PROJECT: PEN-REARED STEELHEAD FROM RIVERINE, ESTUARINE & MARINE RELEASES
PURPOSE: SUPPLEMENTATION ONGOING: N
EVALUATION: QN :
SURVIVAL: RETURNS ARE RIVERINE=7-11%, OCEAN=10% TIDAL--10%
STOCKING DETAILS: FOUR SITES USED, 2 IN RIVER, i IN ESTUARY, 1 IN OCEAN
ACCLIMATION DETAILS: SMOLT RELEASE CONINCIDED WITH MIGRATION OF WILD SMOLTS
OTHER PRE STOCKING INFO: HAT. SM MIGRATING THROUGH WEIR WERE COUNTED W/ WILD SM
IMPACTS; RESEARCH:
IMPACTS; OPINION:
CONTROL DETAILS: WILD FISH
OTHER COMMENTS: WILD FISH WERE SHOCKED FROM KEOUGH R. & PROGENY USED FOR STUDY

238. SPECIES: SH RACE: STOCK(S): NP
MAJOR DRAINAGE: CC SUB DRAINAGE: SAN PABLO BAY
CONTACT: GEORGE CARL PHONE: (707)252-1440
AGENCY: NRS ADDRESS: P.O.BOX 2726, NAPA, CA 94558
PROJECT: NAPA RIVER STEELHEAD ENHANCEMENT PROJECT
PURPOSE: SUPPLEMENTATION, ENHANCE RUNS ONGOING: Y
EVALUATION: QN : SPAWNING GROUND SURVEYS
SURVIVAL: N/A
STOCKING DETAILS: TRUCKED; FIN CLIPPING LAST 3 YEARS
ACCLIMATION DETAILS:
OTHER PRE STOCKING INFO:
IMPACTS; RESEARCH: INCREASE IN ADULT RETURNS
IMPACTS; OPINION:
CONTROL DETAILS:
OTHER COMMENTS: PLANTING EFFORTS HAVE BROADENED THE DISTRIBUTION OF RETURNING
ADULTS TO THE NAPA RIVER BASIN

248. SPECIES: SH RACE: STOCK(S): YK,SK,RI,PR
MAJOR DRAINAGE: CR SUB DRAINAGE: NACHES RIVER
CONTACT: JIM CUMMINS PHONE: (509)575-2740
AGENCY: WDW ADDRESS: 2802 FRUITVALE BLVD., YAKIMA, WA 98902
PROJECT: YAKIMA WDW
PURPOSE: SUPPLEMENTATION, ENHANCE WILD STOCKS ONGOING: Y
EVALUATION: QA : WILD TO HATCHERY SMOLTS, 80% WILD SINCE 1981, SMOLTS AT DAMS
SURVIVAL:
STOCKING DETAILS: TRUCKED
ACCLIMATION DETAILS: NET OFF SECTIONS OF TOPPENISH CR
OTHER PRE STOCKING INFO: YAKIMA ABOVE ROSA NOT STOCKED
IMPACTS; RESEARCH:
IMPACTS; OPINION: NUMBERS WITHIN THE SYSTEM INCREASING
CONTROL DETAILS: N/A
OTHER COMMENTS: LOOKING AT USING WILD STOCKS IN THE FUTURE

A2-5

251. SPECIES: SH RACE: SUM STOCK(S):
MAJOR DRAINAGE: CR SUB DRAINAGE: CLEARWATER RIVER
CONTACT: BILL MILLER PHONE: (208)476-7242
AGENCY: FWS ADDRESS: P.O. BOX 18 AHSAHKA, ID 83520
PROJECT: LOLO CREEK ON THE CLEARWATER RIVER
PURPOSE: SUPPLEMENTATION, ENHANCE RUNS ONGOING: Y
EVALUATION: QA : SNORKLING DATA
SURVIVAL:
STOCKING DETAILS: TRUCKED AND RELEASED
ACCLIMATION DETAILS: SMOLTS ON NF CLEARWATER R. WATER 2-3 WKS PRIOR TO RELEASE
OTHER PRE STOCKING INFO:
IMPACTS; RESEARCH:
IMPACTS; OPINION:
CONTROL DETAILS:
OTHER COMMENTS: ADULTS UNUSED IN HATCHERY EGG TAKES ARE OUTPLANTED THEIR
EFFECTIVENESS IS UNKNOWN

256. SPECIES: SH RACE: SUM STOCK(S): NR
MAJOR DRAINAGE: BC SUB DRAINAGE: NAMAIMO RIVER
CONTACT: BRAIN BLACKMAN PHONE: (604)565-6413
AGENCY: MEBC ADDRESS: 1011 4TH AVE., PRINCE GEORGE, B.C. V2L 3H9
PROJECT: STEELHEAD FRY HEADWATER STOCKING EVALUATION
PURPOSE: SUPPLEMENTATION, ENHANCE PRODUCTION ONGOING: Y
EVALUATION: QN : EVALUATION OF SCATTER VS. POINT RELEASE
SURVIVAL: FRY TO 1+PARR 35 & 48%, EST. 50% FROM 1+ PARR TO SMOLT
STOCKING DETAILS: SCATTER PLANTED W/ BACKPACK NO MORE THAN 500/ GROUP,
ACCLIMATION DETAILS:
OTHER PRE STOCKING INFO: FRY SCATTERED IN 81 WERE DOUBLE THE WT. OF POINT RELS.
IMPACTS; RESEARCH: POINT STOCKING RESULTED IN POOR DISPERSAL & OVERUSE NEAR REL SITES
IMPACTS;.OPINION:
CONTROL DETAILS:
OTHER COMMENTS: WILD BROODSTOCK CAPTURED FROM NANAIMO R. BY HOOK AND LINE, OPTIMUM
STOCKING DENSITIES FOR THIS SYSTEM = 0.4 FRY/SQ. METER @ 1.5 GMS.

257. SPECIES: SH RACE: SUM STOCK(S): SC
MAJOR DRAINAGE: BC SUB DRAINAGE: SILVERHOPE CREEK
CONTACT: BOB GRIFFITH PHONE: (604)387-3660
AGENCY: ADDRESS: VICTORIA, BC
PROJECT: ENHANCEMENT OF SUMMER RUN STEELHEAD IN SILVERHOPE CREEK
PURPOSE: SUPPLEMENTATION ONGOING: N
EVALUATION: QN :
SURVIVAL: SINGLE POINT RELEASES = 63%, SUB SATURATION RELEASES = 77%
STOCKING DETAILS: 5,700 SINGLE POINT RELEASE, 5.700 UNIFORMLY DISTRIBUTED
ACCLIMATION DETAILS:
OTHER PRE STOCKING INFO:
IMPACTS; RESEARCH: POINT RELEASES RESULTED IN FRY BIOMASS DENSITY OF 5.87 G/SQ METER
IMPACTS; OPINION:
CONTROL DETAILS:
OTHER COMMENTS: UPSTREAMING OF LARGE FRY & DOWNSTREAMING OF SMALL FRY WAS EVIDENCED
ABOUT POINT RELEASE SITE, LESS DEFINITE MIGRATIONS FOR SCATTER RELEASES

288. SPECIES: SH RACE: WIN STOCK(S): CH,BG
MAJOR DRAINAGE: WC SUB DRAINAGE: QUILLAYUTE RIVER
CONTACT: BILL FREYMOND PHONE- (206)533-9335
AGENCY: WDW ADDRESS: REGION 6 965 E. HERON, ABERDEEN, WA 98520
PROJECT: QUILIAYUTE
PURPOSE: SUPPLEMENTATION, ENHANCE WILD STOCKS ONGOING: Y
EVALUATION: QN : WILD BROOD RETURN CALCULATED
SURVIVAL: 1-SALT RETURNS=8 20%, 3-SALT=2.30%, OTHER AGES=.48%
STOCKING DETAILS: +/- 100,600 SMOLTS VOLITIONALLY RELASED FROM PONDS
ACCLIMATION DETAILS: REARED TO SMOLTS IN BOGACHIEL & CALAWAH PONDS
OTHER PRE STOCKING INFO: 10-15,000 TRUCKED FROM BOGACHIEL POND TO CALAWAH DRA.
IMPACTS; RESEARCH:
IMPACTS; OPINION: MINIMAL IMPACTS ON WILD FISH DUE TO TIMING DIFFERENCES
CONTROL DETAILS: 622,696 AD & VENT. CLIPS TO AID IN HARVEST MANAG. DETER.
OTHER C014MENTS: WDW CONCERN OF OVERHARVEST ON EARLY WILD FISH ON SOLEDUCK
MOST SPORT HARVEST IS WITHIN 3 MILES OF RELEASE SITE AT BOGACHIEL PONDS.

A2-6

312. SPECIES: SO RACE: STOCK(S):
MAJOR DRAINAGE: AC SUB DRAINAGE: KENAI RIVER
CONTACT: DAVID LITCHFIELD PHONE: (907)262-9369
AGENCY: ADFG ADDRESS: 34828 KALIFORSKY BEACH RD, SUITE B SOLDOTNA, AK 99669
PROJECT: HIDDEN LAKE SOCKEYE SALMON INVESTIGATIONS, 1983-A4
PURPOSE: SUPPLEMENTATION, ENHANCE RUN ONGOING: Y
EVALUATION: QN :
SURVIVAL: FINGERLING TO SMOLT = 20%, SMOLT TO ADULT = 15%
STOCKING DETAILS: STOCKED FINGERLING FROM HATCHERY, ADULTS TAKEN AT LAKE
ACCLIMATION DETAILS:
OTHER PRE STOCKING INFO:
IMPACTS; RESEARCH:
IMPACTS; OPINION: INCREASE PRODUCTION AND ADULT RUN BY PLANTING FINGERLINGS
CONTROL DETAILS:
OTHER COMMENTS: LAKE LACKED ADEQUATE SPAWNING AREA

313. SPECIES: SO RACE,: STOCK(S):
MAJOR DRAINAGE: AC SUB DRAINAGE: KARLUK LAKE
CONTACT: LORNE WHITE PHONE: (907)486-4791
AGENCY: ADFG ADDRESS: 211 MISSIONROAD, KODIAK, AK 99615
PROJECT: SOCKEYE SA114ON REHABILITATION AT UPPER THUMB RIVER, KARLUK LAKE
PURPOSE: SUPPLEMENTATION, ENHANCE NATURAL RUN ONGOING: Y
EVALUATION: QN :
SURVIVAL: EYED EGG PLANT SURVIVAL TO FRY AVERAGED 41.2% (1.4 TO 61.3%)
STOCKING DETAILS: USED AN EGG PLANTING DEVICE, BACKPACKED EGGS TO AREAS
ACCLIMATION DETAILS:
OTHER PRE STOCKING INFO:
IMPACTS; RESEARCH: NO MARKS FOR CONTIBUTION
IMPACTS; OPINION: USED INCREASE IN SPAWNING ESCAPEMENT TO RATE SUCCESS
CONTROL DETAILS:
OTHER COMMENTS: TRIED USING FRY PLANTS BUT HAD PROBLEMS, DISEASE LOOSES AT
HATCHERIES, ETC.

A2-7

APPENDIX A, Part 3. Codes used in data entry and reporting of supplementation projects.

SPECIES RACE STOCK

AS ATLANTIC SALMON MIXED
CM CHUM
BJ BLACKJACK CREEK
CH CHAMBERS CREEK
CW COWLING CREEK
EL ELWHA
EN ENETAI
ES ELSON CREEK
Fl FINCH CREEK
GA GEORAGE ADAMS
GO GOVERS CREEK
GR GREEN RIVER
GS GARRISON SPRINGS
HD HOOD CANAL
ic JOHNS CREEK
KC KETA CREEK
KY KENNEDY CREEK
NO NOOKSACK
NO NISQUALLY
QU QUILCENE
WC WALCOTT
WL WALCOTT SLOUGH
CO COHO
AL ALSEA
BC BIG CREEK
BL BLACK CREEK
CK CLARKS CREEK

ca COQUILLE
CZ COWLITZ
DN DUNGENESS
EL ELWHA
FR FRENCH CREEK
GA GEORGEADAMS
GH GRAYS HARBOR
GR GREEN RIVER
HO HOH
HU HUMPTULIPS
IC INDIAN CREEK
JG JOLLY GIANT CREEK
KL KLASKANINE
KA KALAMA CREEK
LM LOST MAN CREEK
LW LEWIS RIVER HATCHERY
ml MILLSTONE RIVER
MN MINTER CREEK
NO NOOKSACK
NY NOYO
PR PRARIE CREEK
PU PUYALLUP
OC QUILCENE
ON QUINAULT
OU QUINSAM
SD SANDY
SK SKAGIT
so SKOOKUMCHUCK
ST SCOTT RIVER
SR SALMON RIVER
SY SKYKOMISH
Sz SILETZ
TM TEMILE LAKES

A3-1

APPENDIX A, Part 3. Codes used in data entry and reporting of supplernentation projects. (Cont.)

TR TRENT RIVER
WL WALCOTT SLOUGH
WR WALLACE
CH CHINOOK
FAL FALL
AB ABERNATHY
AM AMERICAN RIVER
BC BIG CREEK
BO BONNEVILLE
BT BATTLE CREEK
BW BIG WHITE SALMON
CH CHETCO RIVER
ER EEL RIVER
FT FEATHER RIVER
FW FRESHWATER CREEK
HL HOLLOW CREEK (EEL RIVER)
HR HORSE LINTO CREEK
IC INDIAN CREEK
KM KLAMATH RIVER
LF LYONS FERRY
LR LITTLE RIVER
LW LITTLE WHITE SALMON
mc MERCED RIVER
MD MAD RIVER
MO MOKELUMME RIVER
MT MATTOLE RIVER
RC ROWDY CREEK
RS RUSSIAN RIVER
RW REDWOOD CREEK
SC SPRING CREEK
ST SCOTT RIVER
TN TRINITY RIVER
UR UP RIVER BRIGHT
WM WILLAMETTE
LFA LATE FALL
BT BATTLE CREEK
HP HIGH PRARIE CREEK (KLAMATH)
Om OMAGAR CREEK (KLAMATH)

SPR SPRING
BO BONNEVILLE
CA CARSON
CL CLEARWATER
Cz COWLITZ
EC EAGLE CREEK
ET ENTIAT
FT FEATHER RIVER
HD HOODSPOT
KO KOOSKIA (=CLEAR CREEK)
LE LEAVENWORTH
LW LITTLE WHITE SALMON
MK MCKENZIE
NK NOOKSACK
RG ROUGH RIVER
@Rll RAPID RIVER
SS SOUTH SANTIAM
SU SOLEDUCK
TN TRINITY RIVER
TR TRASK
WM WILLAMETTE
WS WARM SPRINGS
WT WINTHROP

A '3 1)

APPENDIX A, Part 3. Codes used in data entry and, reporting of supplernentation projects. (Cont.)

sum SUMMER
MC Mc CALL
WIN WINTER
SA SACRAMENTO RIVER
UNK UNKNOWN
PIK PINK SALMON
so SOCKEYE
SH STEELHEAD
sum SUMMER
DS DESCHUTES RIVER
DW DWORSHAK "B"
EF EAST FORK "B?'
EL EEL RIVER
HC HELLS CANYON "A"
LE LEAVENWORTH
LF LYONS FERRY
MK MCKENZIE
PA PAHSIMER01 "A"
PB PAHSIMER01 "B"
RS RUSSIAN RIVER
SK SKAMANIA
SS SOUTH SANTIAM
Sw SAWTOOTH "A"
WIN WINTER
AL ALSEA
BC BIG CREEK
CQ COQUILLE
EC EAGLE CREEK
FH FISHHAWK
KL KLASKANINE
KR KEOGH RIVER
MA MAKAH
MF MARION FORKS
NH NEHALEM
NN NORTH NEHALEM
NS NORTH SANTIAM
NU NORTH UMPQUA

UNK UNKNOWN
AC ADOBE CREEK
AM AMERICAN RIVER
BC BIG CREEK
BT BATTLE CREEK
ER EEL RIVER
FT FEATHER RIVER
GR GARCIA RIVER
IC INDIAN CREEK
JG JOLLY GIANT CREEK
MO MOKELUMNE RIVER
NP NAPA RIVER
RC ROWDY CREEK
RS RUSSIAN RIVER
SL SALT CREEK
SM SMITH RIVER
SN SAN LORENZO RIVER
ST SCOTT RIVER
TU TULE
CU CUTTHROATTROUT
SEA SEA-RUN
AL ALSEA
CO COASTAL
SH SHELTON
so STONE LAGOON

APPENDIX A, Part 3. Codes used in data entry and reporting of supplernentation projects. (Cont.)

ANY SPECIES
WI WILD/NATiVE
LINK UNKNOWN
MIXED

EVALUATION NA NOT ATTEMPTED
QN QUANTITATIVE
QA QUALITATIVE

LIFE STAGES DRAINAGE

EG EGG CIR COLUMBIA RIVER
FY FRY PS PUGET SOUND DRAINAGES
FN FINGERLING OC OREGON COAST DRAINAGES
PS PRE-SMOLTS WC WASHINGTON COAST DRAINAGES
Sm SMOLTS BC BRITISH COLUMBIA DRAINAGES
10 1 OCEAN AC ALASKA COAST DRAINAGES
20 2 OCEAN cc CALIFORINA COAST DRAINAGES
30 3 OCEAN SIR SACRAMENTO RIVER
AD ADULTS CT CONNETICUT RIVER
YR YEARLING MR MERRIMACK RIVER
VA VARIABLE MC MAINE COAST DRAINAGES
PR PARR PR PAWCATUCK RIVER

AGENCIES

ABREC ALPHA BIO-RESOURCES ENVIRONMENTAL CONSULTANTS
ADFG ALASKA DEPT. OF FISH AND GAME
BIA BUREAU OF INDIAN AFFAIRS
CCSE CENTRAL COAST SALMON ENHANCEMENT
CDEP CONNETICUT DEPT. OF ENVIRONMENTAL PROTECTION
CDFG CALIFORNIA DEPT. OF FISH AND GAME
CFSO CANADA DEPT. OF FISHERIES AND OCEANS - OPERATIONS
COAPW CITY OF ARCATA-DEPT OF PUBLIC WORKS
CRSA CARMEL RIVER STEELHEAD ASSOCIATION
FBSRA FORT BRAGG SALMON RESTORATION ASSOC.
FOG FRIENDS OF GARCIA
FWS US FISH AND WILDLIFE SERVICE
GRC GARBERVILLE ROTARY CLUB
GRSP GUALALA RIVER STEELHEAD PROJECT
HBCO HUMBOLDT COUNTY
HFAC HUMBOLDT FISH ACTION COUNCIL
HOH HOH INDIAN TRIBE
HSU HUMBOLDT STATE UNIVERSITY
HVBC. HOOPA VALLEY BUSINESS COUNCIL
IDFG IDAHO DEPT. OF FISH AND GAME
LUMM LUMMI INDIAN TRIBE
MBSTP MONTEREY BAY SALMON/TROUT PROJECT
MCFG MENDOCINO COUNTY FISH AND GAME
MEBC MINISTRY OF ENVIRONMENT, BRITISH COLUMBIA
MFM MAKAH FISHERIES MANAGEMENT
MSRSC MAINE SEA RUN SALMON COMMISSION
MUCK MUCKLESHOOT TRIBE
MWSSG MATTOLE WATERSHED SALMON SUPPORT GROUP
NCIDC NORTHERN CALIFORNIA INDIAN DEVELOPMENT COUNCIL
NISQ INISQUALLY INDIAN TRIBE
NOOK NOOKSACKTRIBE
NIRS NAPA RIVER STEELHEAD
ODFW OREGON DEPT. OF FISH AND WILDLIFE
PCFFA PACIFIC COAST FEDERATION FISHERMAN S ASSOC.
PNPT POINT NO POINT TREATY COUNCIL

APPENDIX A, Part 3. Codes used in data entry and reporting of supplementation projects. (Cont.)

PSID PETULUMA SCHOOL DISTRICT
PUT PUYALLUP TRIBE
RHSI RURAL HUMAN SERVICES, INC.
RIDFW RHODE ISLAND DIV. OF FISH AND WILDLIFE
SFU SIMON FRASER UNIVERSITY
SKAG SKAGIT SYSTEMS COOPERATIVE
SOC STATE OF CALIFORNIA
SQAX SQUAXIN TRIBE
SRKC SMITH RIVER KIWANS CLUB
STIL STILLAQUAMISH INDIAN TRIBE
SUQ SUQUAMISH TRIBE
TCSF TYEE CLUB OF SAN FRANCISCO
TULA TULALIP INDIAN TRIBE
USFS US FOREST SERVICE
VDFW VERMONT DEPT. OF FISH AND WILDLIFE
WDIF WASHINGTON DEPT. OF FISHERIES
WDW WASHINGTON DEPT. OF WILDLIFE
YAKI YAKIMA INDIAN TRIBE

A3-5

APPENDIX A

PART 4

Table of all projects included in database (for codes used in data entry and
reporting see Part 3 of Appendix A).

SUPPLEMENTATION REPORT

LIFE MAJOR SUB PRINCIPAL #/YEAR
SPECIES RACE STOCK STAGE DRAINAGE DRAINAGE EVAL AGENCY CONTACT PHONE RELEASED PURPOSE OF PROJECT

1. AS MIXED FY CT ON FWS CARL BARREN (802)826-4438 100000 RESTORATION
2. AS MIXED FY CT ON USFS STEVE ROY (802)773-0300 205000 RESTORATION
3. AS MIXED FY CT ON VDFW KEN COX (802)886-2215 0 RESTORATION
4. AS MIXED SM FY CT ON CDEP STEVE GEBHARD (203)443-0166 0 RESTORATION
5. AS MIXED FY:SM,PR CT FWS TED MEYERS (413)863-3555 2000000 RESTORATION
6. AS MIXED SM,FY,PR MC ON FWS JERRY MARANCIK (207)469-6701 1900000 SUPPLEMENTATION, RESTORATION
7. AS MIXED SM,FY,PR MC ON MSRSC ED BAUM (207)941-4452 1900000 SUPPLEMENTATION, RESTORATION
8. AS MIXED FY,SM,PR MR ON FWS LARRY STOLTE (603)225-1411 1500000 REESTABLISH RUNS
9. AS MIXED PR PR ON RIDFW MARK GIBSON (401)789-0281 400000 RESTORATION
10. CH AD ac ON ABREC J. FEE 2150 SUPPLEMENTATION EVALUATION STUDY
ii. CH FY BC ON CFSO GORDON BEREZAY (604)666-2600 125000 SUPPLEMENTATION
12. CH cc SRKC BOB WILLS (707)487-3443 150000 ENHANCE FISHERIES
13. CH AM SM SR 18040005 ON CDFG RON DUCEY (916)355-0666 4000000 MITIGATION
14. CH BR FY,SM BC ON CFSO GORDON BEREZAY (604)666-2600 107344 SUPPLEMENTATION, ENHANCE RUNS
15. CH CA SM CR 17030001 NA YAKI TOM SCRIBNER (509)865-5121 0 ENHANCE RUN AND FISHERY
16. CH cc SM AC ON ADFG GARY KYLE (907)262-9369 146420 HATCHERY EVALUATION
17. CH cc SM AC ON ADFG NICK DUDIAK (907)235-8191 90000 ENHANCE FISHERY
18. CH cc SM AC ON ADFG NICK DUDIAK (907)235-8191 150000 ENHANCE FISHERY
19. CH cc SM AC ON ADFG NICK DUDIAK (907)235-8191 100000 ENHANCE FISHERY
20. CH CR FN,FY CR 17070105 ODFW LARRY DIMMICK (503)374-8540 900000 MITIGATION
21. CH EG FY AC ON ADFG KEN ROBERSON (907)822-5520 16000 ENHANCE PRODUCTION
22. CH FR PR,SM BC ON SFU G.E. ROSBERG (604)438-1712 0 STOCK EVALUATION
23. CH FT FN cc 18050002 ON TCSF HACK COLLINS (415)454-7754 50000 ENHANCE FISHERY
24. CH Ic SM cc 18010206 ON USFS BILL BEMIS (916)842-6131 7000 PROVIDE SPAWNING HABITAT
25. CH MIXED SM Oc OA ODFW JAY NICHOLAS (503)737-4431 0 RESEARCH
26. CH MT PS'Fw cc 18010108 ON MWSSG GARY PETERSON (707)629-3514 30000 SUPPLEMENTATION, ENHANCE WILD STOCKS
27. CH RC YR cc 18010209 ON SOC TOM GREENER REFER TO TEXT 50000 EDUCATION
28. CH RW YR cc 18010102 ON HBCO STEVE SANDERS (707)488-2253 50000 PROVIDE SALMON FOR.OFF-SHORE FISHERIES
29. CH ST SM cc 18010208 ON USFS JACK WEST (916)842-6131 25000 PROVIDE SPAWNING HABITAT
30. CH TH FRY BC ON CSFO D.C. SEBASTIN ) - 0 HABITAT EVALUATION
31. CH WI SM AC ON ADFG BOB CHLUPACH (907)892-6816 260000 RESEARCH
32. CH WI PS OC 17100304 ON ODFW JAY NICHOLAS (503)737-4431 1000000 RESEARCH
33. CH FAL SM cc 18010102 HFAC JUD ELLINWOOD (707)444-8903 12000 ENHANCE WILD STOCKS
34. CH FAL BC SM CR 17080006 OA ODFW QUENTIN SMITH (503)325-3653 4000000 MITIGATION
35. CH FAL BT Ps'sm SR 18020118 ON FWS GENE FORBES (916)365-8622 16000000 MITIGATION
36. CH FAL CH EG,FY,SM OC 17100306 ON ODFW JAY NICHOLAS (503)737-4431 400000 SUPPLEMENTATION ENHANCE RUNS
37. CH FAL CH SM Oc 17100312 ON ODFW AL MCGIE (503)737-4431 0 RESEARCH, ENHANEE FISHERY
38. CH FAL EL OC NA ODFW GARY SUSAC (503)332-4744 185000 ENHANCE WILD STOCKS
39. CH FAL ER SM cc 18010106 ON CDFG ROYCE GUNTER (707)433-6325 200000 RE-ESTABLISH RUN, ENHANCE RUNS
40. CH FAL ER SM,FY,YR OC 17100306 NA ODFW GARY SUSAC (503)332-4744 1000000 ENHANCE FISHERY
41. CH FAL FT SM SR 18020125 ON CDFG DON SCHLICTING (916)538-2222 12000000 MITIGATION
42. CH FAL FT FY,SM SR 18050002 ON FWS MARTY KJELSON (209)466-4421 800000 STOCKING EVALUATION
43. CH FAL FW YR cc 18010102 ON HFAC CHRISTOPHER TOOLE (707)443-8369 14000 ENHANCE RUNS
44. CH FAL GR,NQ FN PS 17110015 ON NISQ WILLIAM THOMAS (206)456-5221 1317610 ENHANCE FISHERY AND RUN
45. CH FAL GR,PU,DS,ES FN PS 17110019 GA SOAX JOHN BARR (206)426-9783 330792 ESTABLISH FISHERY
46. CH FAL GR,SS FY PS 17110013 NA MUCK DENNIS MOORE (206)939-3311 1606484 PROVIDE FOR FISHERY, UTILIZE HABITAT
47. CH FAL GV,CH,GR,GS SM PS 17110019 ON SUQ PAUL DORN (206)598-3311 1308170 PROVIDE FOR FISHERY
48. CH FAL HD,DS,F1,GA FY,FN PS 17110017 NA PNPT CHRIS WELLER (206)297-3422 872667 ENHANCE RUN AND FISHERY
49. CH FAL HL FN,SM cc 18010106 ON FBSRA WAYNE O'BRYANT (707)925-6458 100000 ENHANCE RUNS, PROVIDE STOCK FOR ELSEWHERE
50. CH FAL HR YR cc 18010112 ON PCFFA MITCH FARRO (707)839-5664 30000 SUPPLEMENTATION, ENHANCE RUNS
51. CH FAL KM YR cc 18010206 ON BIA DELMAR ROBINSON (916)246-5141 9000 RE-ESTABLISH RUNS
52. CH FAL LR SM cc 18010108 ON PCFFA MITCH FARRO (707)839-5664 50000 SUPPLEMENTATION, ENHANCE RUNS
53. CH FAL MA FN PS 17110019 ON FWS DAVID ZAJAC (206)753-9460 450000 ENHANCE RUNS
54. CH FAL MC SM,YR cc 18040009 ON CDFG MICHAEL COZART (209)563-6410 800000 MITIGATION
55. CH FAL MD YR cc 18010105 ON CDFG BRUCE BARNGROVER (707)822-0592 200000 ENHANCE RUNS
56. CH FAL MO SM cc 18050002 ON CDFG DON ESTEY (209)759-3383 2500000 MITIGATION, ENHANCEMENT
57. CH FAL NO,GR,SM,SO FN,PS PS 17110004 ON LUMM STEVE SEYMOUR (206)734-8180 1242593 ENHANCE FI HERIES
58. CH FAL PU,GR,DS FN PS 17110014 NA PUT RUSSELL LADLEY (206)593-0254 384002 ENHANCE FISHERIES
59. CH FAL SS, GR FN,FR PS 17110013 OA MUCK DENNIS MOORE (206)939-3311 387630 PROVIDE FOR FISHERIES,
60. CH FAL SY,GR,sm FN PS 17110019 ON TULA CLIFF BENGSTON (206)653-7477 925000 PROVIDE FOR FISHERIES
61. CH FAL TN SM,YR cc 18010212 ON CDFG GERALD BIDELL (916)778-3931 1400000 MITIGATION
62. CH FAL TN YR cc 18010212 ON HVBC MICHAEL ORCUTT (916)625-4268 35000 ENHANCE RUNS
63. CH FAL UM,AL SM OC 17100303 NA ODFW JERRY SWAFFORD (503)496-3484 100000 ENHANCE WILD STOCKS
64. CH FAL LINK FN SR 18020104 ON FWS JAMES SMITH (916)527-3043 50000 HATCHERY EVALUATION

SUPPLEMENTATION REPORT

LIFE MAJOR SUB PRINCIPAL #/YEAR
SPECIES RACE STOCK STAGE DRAINAGE DRAINAGE EVAL AGENCY CONTACT PHONE RELEASED PURPOSE OF PROJECT

65. CH FAL UR SM CR 17030001 NA YAKI T014 SCRIBNER (509)865-5121 302000 ENHANCE RUN
66. CH FAL URB FY,FN CR 17080001 NA WDF DICK JOHNSON (206)837-3311 0HABITAT UTILIZATION
67. CH LFA HP SM cc 18010208 NA NCIDC RONNIE PIERCE (707)839-3637 15000 RE-ESTABLISH RUNS
68. CH LFA KM PS cc 18010208 ON NCIDC WALTER LARA JR. (707)482-4535 8000 RE-ESTABLISH RUNS, TRIBAL FISHERY
69. CH LFA OM WM cc 18010208 NA NCIDC RONNIE PIER6E (707)839-3637 15000 RE-ESTABLISH RUNS
70. CH LFA SA YR SR 18020118 ON FWS GENE FORBES (916)365-8622 900000 MITIGATION, ESTABLISH RUN
71. CH SPR PR BC CFSO GORDON BEREZAY (604)666-8648 0HATCHERY EVALUATION
72. CH SPR SM,FY,PS CR 17030001 ON YAKI DAVE FAST (509)865-5121 100000 ENHANCE RUNS
73. CH SPR FN,SM CR FWS BILL MILLER (208)476-7242 200000 SUPPLEMENTATION, ENHANCE RUNS
74. CH SPR SM,FN CR FWS BILL MILLER (208)476-7242 375000
75. CH SPR FY,FN,SM,AD CR IDFG BURT BOWLER (208)743-6502 80000
76. CH SPR FY,EG CR IDFG DICK SKULLY (208)334-3791 99900 ESTABLISH RUN
77. CH SPR FR PR BC ON CFSO GORDON BEREZAY (604)666-8646 0EVALUATION
78. CH SPR FT SM SR 18020125 ON CDFG DON SCHLICTING (916)538-2222 2000000 MITIGATION
79. CH SPR HD,CZxNK,SU SM PS 17110018 ON FWS DAVID ZAJAC (,206)753-9460 150000 ASSIST THREATENED SPECIES
80. CH SPR LE FN,FY CR 17020011 FWS JIM MULLEN (509)548-7573 780000 ENHANCE WILD STOCKS
81. CH SPR LO AD CR 17060104 ON ODFW RICH CARMICHAEL (503)963-1777 0PROVIDE TRIBAL ADULTS
82. CH SPR MK Ps'sm CR 17090004 QA ODFW SCOTT LUSTED (503)896-3513 1100000 MITIGATION
83. CH SPR NO FN,PS PS 17110004 GA LUMM STEVE SEYMOUR (206)734-8180 80719 ESTABLISH FISHERY
84. CH SPR NO FY PS 17110004 NA NOOK PAT PETUCHOV (206)592-5176 200000 PROVIDE FOR FISHERY
85. CH SPR RG AD OC 17100307 ON ODFW MIKE EVENSON (503)878-2235 0RESEARCH, ENHANCE RUNS AND FISHERY
86. CH SPR RG SM OC 17100307 ON ODFW MIKE EVENSON (503)878-2235 100000 ENHANCE FISHERY
87. CH SPR SS FY CR 17090004 NA OOFW DENNIS WISE (503)378-6925 400000 EDUCATION, ENHANCEMENT
88. CH SPR TN SM,YR cc 18010212 ON CDFG GERALD BIDELL (916)778-3931 2000000 MITIGATION
89. CH SPR TR FY Oc OA ODFW JOHN CASTEEL (503)842-2741 200000 ENHANCEMENT
90. CH SPR WM Ps'sm CR 17090009 ON ODFW 808 SOHLER (503)782-2933 3300000 MITIGATION
91. CH SPR WM Ps CR 17090001 ON ODFW MAX SMITH (503)726-3517 1000000 MITIGATION
92. CH sum SM CR IDFG KENT BALL (208)756-2271 950000
93. CH SUM SF FY CR 17060208 ON IDFG DICK SKULLY (208)334-3791 178640 ESTABLISH RUN
94. CH SUM ST FN PS 17110008 OA STIL KIP KILLEBREW (206)435-8770 81093 SUPPLEMENTATION, ENHANCE RUNS
95. CH LINK YR cc 18060006 CCSE PAUL CLEVELAND (805)773-3316 50000 ESTABLISH RUN
96. CH LINK ER SM cc 18010106 PCFFA SCOTT DOWNIE (707)923-3459 100000 REESTABLISH RUNS
97. CH WIN SA PS SR 18020103 ON FWS GENE FORBES (916)365-8622 0ASSIST THREATENED SPECIES
98. CM FY AC ADFG TOM KOHLER 469000 HARVEST AUGMENTATION
99. cm FY AC ON ADFG JOHN MCNAIR 3549811 EVALUATION
100. cm CL FY CR 17090007 NA ODFW WAYNE BOWERS (503)657-6822 0ENHANCE WILD STOCKS
101. Cm EL,QC,WL,EN EG,FY PS 17110019 QA PNPT CHRIS WELLER (206)297-3422 1166286 ENHANCE RUN AND FISHERY
102. CM ES,JC FY,EG PS 17110019 ON SOAX JOHN BARR (206)426-9783 402767 ESTABLISH FISHERY INITIALIZE RUN
103. CM FI,HD ,GR,KC FY PS 17110013 ON MUCK DENNIS MOORE (206)939-3311 530350 PROVIDE FOR FISHEky
104. CM FI,KC FY PS 17110013 ON MUCK DENNIS MOORE (206)939-3311 114467 PROVIDE FOR FISHERIES
105. CM MA FY PS 17110019 NA FWS DAVID ZAJAC (206)753-9460 1400000 ENHANCE RUNS M
106. CM NO AC GA ADFG JIM RAYMOND (907)452-1531 750000 RESEARCH
107. CM NO FY,EG PS 17110004 ON NOOK GARY MACWILLIAMS (206)592-5176 81000 ENHANCE FISHERY
108. CM NO FY PS 17110004 QA NOOK GARY MACWILLIAMS (206)592-5176 299275 PROVIDE FOR FISHERIES DEVELOP SURPLUS
109. CM NO,QC FY PS 17110004 QA LUMM STEVE SEYMOUR (206)734-8180 183859 DEVELOP SURPLUS FOR SfOCKING
110. cm PU,HD,GA,CH FY PS 17110014 GA PUT RUSSELL LADLEY (206)593-0254 325050 ENHANCE FISHERIES
ill. cm ST FY PS 17110008 ON STIL KIP KILLEBREW (206)435-8770 460450 ENHANCE FISHERIES, INITIALIZE RUNS
112. CM wC FY PS 17110018 NA FWS DAVID ZAJAC (206)753-9460 2300000 PROVIDE TRIBAL ADULTS
113. CM WL FY PS 17110018 ON FWS DAVID ZAJAC (206)753-9460 3693760 ENHANCE FISHERIES
114. CM ENL CW,GO,BJ EG,FY PS 17110019 OA SUO PAUL DORN (206)598-3311 3620000 REESTABLISH FISHERY
115. CM L NO EG PS 17110015 OA NISQ WILLIAM THOMAS (206)456-5221 542133 REESTABLISH RUNS
116. CM N KY FR,EG PS 17110015 QA NISQ WILLIAM THOMAS (206)456-5221 312760 REESTABLISH RUNS
117. CM N,L ES,JC,GS FY,EG PS 17110019 OA SQAX JOHN BARR (206)426-9783 1906732 ESTABLISH FISHERY, REESTABLISH RUNS
118. CM N,L WL FY PS 17110019 ON TULA CLIFF BENGSTON (206)653-7477 4000000 PROVIDE FOR FISHERIES
119. CO FN AC ON ADFG JIM RAYMOND (907)452-1531 125000 RESEARCH
120. CC FY BC ON CFSO ROBERT HURST (604)756-7296 9500 SUPPLEMENTATION STOCK EVALUATION
121. CC FN cc 18010102 HFAC JUD ELLINWOOD (707)444-8903 25000 ENHANCE WILD ST6CKS
122. CO YR cc 18010102 QA COAPW DAVID HULL (707)822-5957 1500 ENHANCE RUNS
123. CO FY CR 17020011 FWS JIM MULLAN (509)548-7573 61800 SMOLT PRODUCTION
124. CO FN CR 17080002 NA WDF ROBIN NICHOLAY (206)225-7413 2000000 ENHANCE RUNS (HATCHERY)
125. CO YR PS 17110008 WDF JIM AMES (205)753-0196 0SUPPLEMENT TRIBAL,COMMERCIAL,NON-INDIAN SPORT FISHERY
126. CO AL sm OC 17100205 ON ODFW MARIO SOLAZZI (503)737-4431 300000 RESEARCH
127. CC AL,SZ,CO FY OC 17100206 ON ODFW MARIO SOLAZZI (503)737-4431 0RESEARCH
128. CO BC SM CR 17080006 ODFW DAVE RIEBEN (503)458-6512 0MITIGATION

SUPPLEMENTATION REPORT

LIFE MAJOR SUB PRINCIPAL #/YEAR
SPECIES RACE STOCK STAGE DRAINAGE DRAINAGE EVAL AGENCY CONTACT PHONE RELEASED PURPOSE OF PROJECT

129. CC BC,ST SM cc 18060012 ON MBSTP DAVE STREIG (408)458-3095 3000 ENHANCE WILD STOCKS, DEVELOP SURPLUS
130. CC BG FN,PS,SM AC ON ADFG BOB CHLUPACH (907)892-6816 1500000
131. CC cc FN AC ON ADFG NICK DUDIAK (907)235-8191 200000 ENHANCE FISHERY
132. CO cc SM AC ON ADFG NICK DUDIAK (907)235-8191 120000 ENHANCE FISHERY
133. CO CH BC QN CFSO MATTHEW FOY (604)666-3678 0 INCREASE HABITAT
134. co CK FY PS 17110004 ON WOF DON HENDRICK (206)336-9538 160500 RESEARCH, MITIGATION
135. CC CK FY PS 17110004 ON WDF DON HENDRICK (206)336-9538 78700 RESEARCH, MITIGATION
136. co CK FY PS 17110004 ON WDF DON HENDRICK (206)336-9538 65400 RESEARCH MITIGATION
137. CO CK,WL,GA,WR SM PS 17110015 ON NISO WILLIAM THOMAS (206)456-5221 395800 PROVIDE POR FISHERY
138. CO CM SM WC 17100204 QN ODFW MARIO SOLAZZI (503)737-4431 240000 RESEARCH
139. CC CR SM CR NA ODFW WAYNE STENDROSKY (503)374-8381 850000 INITIALIZE RUN
140. CC EL FY si 17110020 OA PNPT CHRIS WELLER (206)297-3422 788060 ENHANCE RUN AND FISHERY
141. CC EL,DN FY si 17110021 QA PNPT CHRIS WELLER (206)297-3422 94500 ENHANCE RUN AND FISHERIES, RESEARCH
142. CC FC SM'Ps Oc 17100205 ODFW TIM SCHAMBER (503)487-4152 0 ENHANCE FISHERY
143. CC FR FY sc ON CFSO ROBERT HURST (604)756-7296 10000 HABITAT EVALUATION
144. CC HL YR cc 18010106 GRC JIM JOHNSON (707)928-2293 15000 REESTABLISH RUNS
145. CC HO,QN FY,FN WC 17100101 QN HOH JIM JORGENSEN (206)374-6582 83942 ENHANCE FISHERIES
146. CC HU FY WC 17100103 ON WDF DAVE SEILER (206)586-1994 132000
147. CC Ic FN,YR cc 18010206 ON USFS BILL BEMIS (916)842-6131 7000 PROVIDE SPAWNING HABITAT
148. CO JG FN,YR cc 18010102 ON COAPW DAVID HULL (707)822-5957 5000 REESTABLISH RUNS, RESEARCH
149. Co KL,BC SM CR 17080006 OA ODFW QUENTIN SMITH (503)325-3653 1400000 MITIGATION
150. CC LM YR cc 18010102 ON HBCO STEVE SANDERS (707)488-2253 100000 PROVIDE SALMON FOR OFF-SHORE FISHERIES
151. CC LR FY cc 18010108 ON PCFFA MITCH FARRO (707)839-5664 15000 INITIALIZE RUN, EDUCATION
152. Co LS SM,FN AC ON ADFG BOB CHLUPACH (907)892-6816 450000
153. CO MA FY PS 17110019 MFM MARK LARIVIERE (206)645-2201 244531 ENHANCE FISHERY
154. Co 14A S14 Ps 17110019 ON FWS DAVID ZAJAC (206)753-9460 265000 ENHANCE RUNS (HATCHERY)
155. CO MI Fy BC ON CFSO ROBERT HURST (604)756-7296 26000 HABITAT UTILIZATION
156. CC MI FY PS 17110019 OA SUO PAUL DORN (206)598-3311 335370 ENHANCE FISHERY
157. CC MI SM PS 17110019 OA SUQ PAUL DORN (206)598-3311 57053 PROVIDE FOR FISHERY, ENHANCE FISHERY
158. CC MI,PU,WR,KA FY PS 17110015 ON NISO WILLIAM THOMAS (206)456-5221 332600 INITIALIZE RUNS
159. CC MIXED SM Oc QA ODFW JAY NICHOLAS (503)737-4431 0 RESEARCH
160. CO MN FY FN PS 17110019 ON WDF CHUCK BARANSKI (206)753-0197 25000 RESEARCH
161. CC MT YR:SM cc 18010108 ON MWSSG GARY PETERSON (707)629-3514 8000 SUPPLEMENTATION, ENHANCE WILD STOCKS
162. CC NE SM,FY OC 17100202 ODFW GARY YEAGER (503)368-6828 800000 ENHANCE WILD STOCKS
163. CO NO,SY,SK,SO FN,PS PS 17110004 ON LUMM STEVE SEYMOUR (206)734-8180 1014080 ENHANCE FISHERY
164. CC NY YR cc 18010102 ON CDFG ALLAN GRASS (707)743-1535 30000 ENHANCE RUNS, DEVELOP STOCKS
165. CC NY YR cc 18010105 ON CDFG BRUCE BARNGROVER (707)822-0592 225000 INITIATE AND ENHANCE RUNS
166. CC NY,PR YR cc 18010102 ON HFAC CHRISTOPHER TOOLE (707)443-8369 22000 ENHANCE RUNS
167. CC PU FY PS 17110014 QA PUT RUSSELL LADLEY (206)593-0254 269455 ENHANCE FISHERIES
168. CO Qc SM PS 17110018 ON FWS DAVID ZAJAC (206)753-9460 500000 ENHANCE FISHERIES
169. CC QU,BL FY BC ON CFSO ROBERT HURST (604)756-7296 8500 ENHANCE RUNS
170. CC RC YR cc 18010209 ON SOC TOM GREENER REFER TO TEXT 4000 EDUCATION
171. CC RS FN,YR cc 18010106 ON CDFG ROYCE GUNTER (707)433-6325 120000 MITIGATION
172. CC SD FY CR 17090008 ON ODFW DENNIS WISE (503)378-6925 750000 EDUCATION, INITIALIZE RUN
173. CC SN SM cc 18060005 ON MBSTP DAVE STREIG (408)845-3095 20000 ENHANCE RUNS
174. Co SR SM,AD CR 17080001 ODFW DICK WHITLATCH (503)668-4222 0 MITIGATION
175. CC SR FY CR 17090007 NA ODFW WAYNE BOWERS (503)657-6822 0 ENHANCE WILD STOCKS
176. CC ST FN,YR cc 18010208 ON USFS JACK WEST (916)842-6131 15000 PROVIDE SPAWNING HABITAT
177. CC ST,SK FN PS 17110008 OA STIL KIP KILLEBREW (206)435-87'70 46999 ENHANCE FISHERIES
178. CC SY,SK SM PS 17110019 ON TULA CLIFF BENGSTON (206)653-7477 718000 PROVIDE FOR FISHERIES
179. CC TM FY,SM OC 17100304 ON ODFW PAUL REIMERS (503)888-5515 30000 RESEARCH, ENHANCE RUNS
180. CC TM Ps'sm OC 17100304 ON ODFW PAUL REIMERS (503)888-5515 180000 SUPPLEMENTATION, ENHANCE WILD STOCKS
181. CC TM,NY SM,YR cc 18010209 SRKC BOB WILLS (707)487-3443 10000 ENHANCE RIVER & OCEAN FISHERIES
182. CC TR FY sc ON CFSO ROBERT HURST (604)756-7296 7500 SUPPLEMENTATION
183. CC WA SM CR 17070106 NA WDF DICK JOHNSON (206)837-3311 2500000 ENHANCE RUNS (HATCHERY)
184. CC FAL CZ FN CR 17070105 ON WDF DAVE SEILER (206)586-1994 505000 PASSAGE EVALUATION
185. CC FAL CZ FN CR 17070105 ON WDF DAVE SEILER (206)586-1994 0 PASSAGE EVALUATION
186. co FAL DN SM PS 17110018 ON WDF TIM FLINT (206)753-0198 64850 HATCHERY EVALUATION
187. CC FAL DN FY PS 17110018 ON WDF TIM FLINT (206)753-0198 27447
188. CC FAL GH FN WC 17100103 ON WDF RICK BRIX (206)249-4628 716000 RESEARCH
189. Co FAL GH SM WC 17100105 ON WDF RICK BRIX (206)249-4628 0 EVALUATION
190. Co FAL GH PS WC 17100105 ON WDF RICK BRIX (206)249-4628 257000 EVALUATION
191. Co FAL GR FY PS 17110019 QA WDF TIM FLINT (206)753-0198 58000 HATCHERY EVALUATION
192. CC FAL GR FY Ps 17110013 ON WDF DAVE SEILER (206)586-1994 3099080 PASSAGE EVALUATION

SUPPLEMENTATION REPORT

LIFE MAJOR SUB PRINCIPAL #/YEAR
SPECIES RACE STOCK STAGE DRAINAGE DRAINAGE EVAL AGENCY CONTACT PHONE RELEASED PURPOSE OF PROJECT

193. CO FAL GR,PU SM PS 17110015 ON WDF TIM FLINT (206)753-0198 196750
194. CO FAL HU PS wC 17100105 ON WDF RICK BRIX (206)249-4628 0RESEARCH
195. CO FAL LW FY,SN CR 17080002 ON WDF GREG JOHNSON (206)753-3956 161805 RESEARCH
196. CO FAL MI FN PS 17110019 ON WOF TIM FLINT (206)753-0198 36000 RESEARCH
197. CO FAL PU SM PS 17110015 ON WDF TIM FLINT (206)753-0198 53150 HATCHERY EVALUATION
198. CO FAL PU,MI FY PS 17110016 ON WDF TIM FLINT (206)753-0198 1457265 ENHANCE RUNS
199. CO FAL QC,MI FY PS 17110018 ON WDF RICH KOLB (206)586-9344 0
200. CO FAL SO FY Wc 17100101 ON WDF DAVE SEILER (206)586-1994 0HATCHERY EVALUATION
201. CO FAL SD,QT FY wC 17100101 ON WDF DAVE SEILER (206(586-1994 0HATCHERY EVALUATION
202. CO FAL SD,SR FY wC 17100102 ON WDF DAVE SEILER (206)586-1994 123731 HATCHERY EVALUATION
203. CO FAL SY SM PS 17110016 ON WDF TIM FLINT (206)753-0198 0ENHANCE RUN
204. CO FAL TOUTLE FN CR 17080005 ON WDF GREG JOHNSON (206)753-3956 1200000 MITIGATION ENHANCE FISHERIES
205. CU SEA CO SM,FN wC 17100103 GA WDW BILL FREYMOND (206)533-9335 23400 PROVIDE FOA FISHERY
206. CU SEA CO SM,FN WC 17100104 QA WDW BILL FREYMOND (206)533-9335 26090 PROVIDE FOR FISHERY
207. CU SEA CO SM,FN WC 17100105 OA WDW BILL FREYMOND (206)533-9335 7325 PROVIDE FOR FISHERY
208. CU SEA CO SM FN WC 17100105 GA WDW BILL FREYMOND (206)533-9335 6792 PROVIDE FOR FISHERY
209. CU SEA CO SM:FN WC 17100101 OA WDW BILL FREYMOND (206)533-9335 3000 PROVIDE FOR FISHERY
210. CU SEA RW YR cc 18010102 OA HBCO STEVE SANDERS (707)4a8-2253 500 SUPPLEMENTATION, ENHANCE WILD STOCKS
211. CU SEA SH SM,FN PS 17110019 OA WDW BILL FREYMOND (206)533-9335 1000 PROVIDE FOR FISHERY
212. CU SEA SH sm PS 17110018 GA WDW BILL FREYMOND (206)533-9335 29905 PROVIDE FOR FISHERY
213. CU SEA SH SM,FN PS 17110017 OA WDW BILL FREYMOND (206)533-9335 35820 PROVIDE FOR FISHERY
214. CU SEA SO YR cc 18010102 ON HSU ERIC LOUDENSLAGER (707)826-3445 40000 ESTABLISH FISHERY
215. PK FY AC ON ADFG TIM MCDANIEL 1200000 ESTABLISH A RUN
216. PK AC ON ADFG TOM KOHLER 0HARVEST AUGMENTATION
217. PK ST FY PS 17110008 ON STIL KIP KILLEBREW (206)435-8770 172500 ENHANCE FISHERIES
218. PK TU FY AC ON ADFG NICK DUDIAK (907)235-8191 300000 ENHANCE FISHERY
219. SH FY BC ON MEBC JEREMY HUME (604)660-1812 0SUPPLEMENTATION
220. SH SM,YR cc 18010109 NA GRSP DON MCDONALD (707)884-3884 30000 ENHANCE WILD STOCKS
221. SH AC FN,YR cc 18010110 NA PSD TOM FURRE (707)778-4703 0REESTABLISH RUNS
222. SH AL sm Oc ON ODFW KEN KENASTON (503)737-4431 280000 RESEARCH
223. SH AM TY SR 18040005 ON CDFG RON DUCEY (916)355-0666 450000 MITIGATION
224. SH AR SM,FN AC ADFG NICK DUDIAK (907)235-8191 10000 ENHANCE FISHERY
225. SH BC,ST SM cc 18060012 ON MBSTP DAVE STREIG (408)458-3095 5000 ENHANCE WILD RUNS
226. SH CM YR CR 17020008 ON WDW JOE FOSTER (506)754-4624 0MITIGATION
227. SH CR PS,SM,20,30 CC 18060012 NA CRSA ROY THOMAS (408)625-2255 14000 ENHANCE WILD STOCKS
228. SH ER YR cc 18010106 GRC JIM JOHNSON (707)923-2293 25000 REESTABLISH RUNS
229. SH ER YR cc 18010102 ON HBCO STEVE SANDERS (707)488-2253 50000 ENHANCE IN-RIVER FISHERY
230. SH FT FN,YR SR 18020125 ON CDFG DON SCHLICTING (916)538-2222 3000000 MITIGATION -
231. SH GR YR cc 18010108 NA FOG CRAIG BELL (707)882-2150 30000 ENHANCE WILD STOCKS
232. SH Ic YR cc 18010206 ON USFS BILL BEMIS (916)842-6131 250 PROVIDE SPAWNING HABITAT
233. SH ic FN,YR cc 18010102 ON COAPW DAVID HULL (707)822-5957 2000 REESTABLISH RUNS, RESEARCH
234. SH KR SM BC ON MEBC BRUCE WARD (604)660-1812 20000 SUPPLEMENTATION
235. SH MA FY PS 17110019 MFM MARK LARIVIERE (206)645-2201 96359 ENHANCE FISHERY
236. SH MD YR cc 18010105 NA CDFG BRUCE BARNGROVER (707)822-0592 400000 ENHANCE RUNS
237. SH MO YR cc 18050002 NA CDFG DON ESTEY (209)759-3383 50000 MITIGATION, ENHANCEMENT
238. SH NP YR cc 18050002 ON NRS GEORGE CARL (707)252-1440 7000 SUPPLEMENTATION, ENHANCE RUNS
239. SH RC YR cc 18010209 soc TOM GREENER REFER TO TEXT 50000 EDUCATION
240. SH RS YR cc 18010109 NA MCFG BILL TOWNSEND (707)462-5228 70000 ENHANCE WILD STOCKS
241. SH RS YR cc 18010106 NA CDFG ROYCE GUNTER (707)433-6325 200000 MITIGATION
242. SH SM PS sc 18010209 NA RHSI DENNIS CONGER (707)464-7441 800 EDUCATION
243. SH SMITH RIVER cc SRKC BOB WILLS (707)487-3443 75000 ENHANCE FISHERIES
244. SH SN SM cc 18060005 ON MBSTP DAVE STREIG (408)458-3095 40000 ENHANCE RUNS
245. SH ST VA cc 18010208 ON USFS JACK WEST (916)a42-6131 400 PROVIDE SPAWNING HABITAT
246. SH TU,BC,SL YR cc 18010112 ON DAVID REIELS (916)628-5012 6000 RESCUE STRANDED FISH
247. SH VA SM Oc ON ODFW KEN KENASTON (503)737-4431 1000000 RESEARCH
248. SH YK,SK,R1,PR SM,FY CR 17030002 OA WDW JIM CUMMINS (509)575-2740 0SUPPLEMENTATION, ENHANCE WILD STOCKS
249. SH sum FN CR ON IDFG KENT BALL (208)756-2271 790000
250. SH sum SM AD CR 17060305 ON FWS BILL MILLER (208)476-7242 1200000 MITIGATION
251. SH sum AD:FY,SM CR OA FWS BILL MILLER (208)476-7242 1000000 SUPPLEMENTATION, ENHANCE RUNS
252. SH SUM CH sm PS 17110015 QA WDW BOB LELAND (206)753-5700 23632 PROVIDE FOR FISHERY, ENHANCE WILD STOCKS
253. SH SUM DS SM CR 17070306 ON ODFW JIM NEWTON (503)296-4628 162000 MITIGATION
254. SH SUM DS SM CR 17070306 ON ODFW BOB LINDSAY (503)737-4431 127000 RESEARCH, ENHANCE FISHERY
255. SH SUM MK,SS SM CR 17090004 OA ODFW SCOTT LUSTED (503)896-3513 120000 MITIGATION
256. SH SUM NR FY BC ON MEBC BRAIN BLACKMAN (604)565-6413 23550 SUPPLEMENTATION, ENHANCE PRODUCTION

SUPPLEMENTATION REPORT

LIFE MAJOR SUB PRINCIPAL #/YEAR
SPECIES RACE STOCK STAGE DRAINAGE DRAINAGE EVAL AGENCY CONTACT PHONE RELEASED PURPOSE OF PROJECT

257. SH sum SC FY BC ON BOB GRIFFITH (604)387-3660 11400 SUPPLEMENTATION
258. SH SUM SK SM CR, 17090004 QA OOFW JOHN HOSKINS (503)896-3294 108000 INITIALIZE RUN, ENHANCE RUN
259. SH SUM SK SM Oc 17090006 OOFW GREG LIPSIEA (503)367-3437 220000 MITIGATION
260. SH SUM SK SM PS 17110005 QA WOW BOB LELAND (206)753-5700 25350 PROVIDE FOR FISHERY
261. SH SUM SR SM,FY,FN,AD CR QA IDFG KENT BALL (208)756-2271 900000 REESTABLISH RUN, RELOCATION
262. SH WIN FY CR 17090007 NA ODFW WAYNE BOWERS (503)657-6822 0ENHANCE WILD STOCKS
263. SH WIN SM'Ps OC 17090008 ODFW LYLE CURTIS (503)994-8606 80000 REESTABLISH RUNS
264. SH WIN AL SM OC 17100304 ODFW PAUL REIMERS (503)888-5515 30000 INITIALIZE RUN, ENHANCE RUNS
265. SH WIN AL,CQ SM OC 17100205 ODFW TERRY FISHER (503)487-7240 675000 ENHANCEMENT
266. SH WIN BC SM CR 17080003 ODFW MEL KELLY (503)455-2234 570000 MITIGATION
267. SH WIN BC SM Oc 17090005 ODFW DAN BARRETT (503)394-2496 75000 ENHANCE RUNS
268. SH WIN BC KL SM CR 17080006 QA ODFW QUENTIN SMITH (503)325-3653 650000 MITIGATION
269. SH W N BG:QN,CH Sm Wc 17100105 ON WOW BILL FREYMOND (206)533-9335 85825 PROVIDE FOR FISHERY, ENHANCE WILD STOCKS
270. SH WIN BT,SA YR SR 18020118 ON FWS GENE FORBES (916)365-8622 1000000 MITIGATION
271. SH WIN CC sm OC 17090008 ODFW CHARLIE STANLEY (503)392-3485 340000 ENHANCE RUN
272. SH WIN CH SM PS 17110019 QA SOAX JOHN BARR (206)426-9783 44258 ESTABLISH FISHERY
273. SH WIN CH SM PS 17110018 ON WDW BILL FREYMOND (206)533-9335 80840 PROVIDE FOR FISHERY, ENHANCE WILD STOCKS
274. SH WIN CH SM PS 17110017 ON WOW BILL FREYMOND (206)533-9335 24310 PROVIDE FOR FISHERY, ENHANCE WILD STOCKS
275. SH WIN CH SM PS 17110014 ON WDW BOB LELAND (206)753-5700 142080 PROVIDE FOR FISHERY, ENHANCE WILD STOCKS
276. SH WIN CH SM PS 17110013 ON WOW BOB LELAND (206)753-5700 192580 PROVIDE FOR FISHERY, ENHANCE WILD STOCKS
277. SH WIN CH Sm PS 17110012 ON WDW BOB LELAND (206)753-5700 58515 PROVIDE FOR FISHERY, ENHANCE WILD STOCKS
278. SH WIN CH SM PS 17110007 ON WDW 808 LELAND (206)753-5700 248260 PROVIDE FOR FISHERY, ENHANCE WILD STOCKS
279. SH WIN CH SM PS 17110002 ON WDW BOB LELAND (206)753-5700 37255 PROVIDE FOR FISHERY, ENHANCE WILD STOCKS
280. SH WIN CH SM PS 17110019 QA TULA CLIFF BENGSTON (206)653-7477 60000 PROVIDE FOR FISHERIES
281. SH WIN CH sm PS 17110019 ON WOW BOB LELAND (206)753-5700 22667 PROVIDE FOR FISHERY
282. SH WIN CH SM PS 17110016 ON WOW BOB LELAND (206)753-5700 35000 PROVIDE FOR FISHERY
D> 283. SH WIN CH SM PS 17110008 OA WOW BOB LELAND (206)753-5700 110425 PROVIDE FOR FISHERY
4@1 284. SH WIN CH SM si 17110020 ON WOW BILL FREYMOND (206)533-9335 3610 PROVIDE FOR FISHERY ENHANCE WILD STOCKS
285. SH WIN CH SM si 17110020 ON WDW BILL FREYMOND (206)533-9335 69100 PROVIDE FOR FISHERY: MITIGATION
286. SH WIN CH SM si 17110021 ON WDW BILL FREYMOND (206)533-9335 63925 PROVIDE FOR FISHERY, ENHANCE WILD STOCKS
287. SH WIN CH SM WC 17100104 ON WOW BILL FREYMOND (206)533-9335 17795 ENHANCE FISHERY AND WILD STOCKS
288. SH WIN CH,BG SM,FY WC 17100101 ON WOW BILL FREYMOND (206)533-9335 171711 SUPPLEMENTATION, ENHANCE WILD STOCKS
289. SH W N CH,NO SM PS 17110004 ON WOW BOB LELAND (206)753-5700 115600 PROVIDE FOR FISHERY
290. SH WIN CH,SK SM PS 17110007 QA SKAG JIM GIBSON (206)466-3163 50000 ENHANCE FISHERY
291. SH WIN CH,SN SM PS 17110009 QA WOW BOB LELAND (206)753-5700 339925 PROVIDE FOR FISHERY, ENHANCE WILD STOCKS
292. SH N CH SN SM PS 17110010 OA WDW BOB LELAND (206)753-5700 339925 PROVIDE FOR FISHERY ENHANCE WILD STOCKS
293. SH WWIN CH:SN sm PS 17110011 OA WDW 808 LELAND (206)753-5700 339925 PROVIDE FOR FISHERY: ENHANCE WILD STOCKS,
294. SH WIN CH,SO SM WC 17100104 ON WOW BILL FREYMOND (206)533-9335 65793 PROVIDE FOR FISHERY, ENHANCE WILD STOCKS, MITIGATION
295. SH WIN CH'VW SM Wc 17100104 ON WOW BILL FREYMOND (206)533-9335 11250 PROVIDE FOR FISHERY, ENHANCE WILD STOCKS
296. SH W 1 N CH WK Sm Wc 17100104 ON WOW BILL FREYMOND (206)533-9335 51492 PROVIDE FOR FISHERY, ENHANCE WILD STOCKS
297. SH W CH:WY SM Wc 17100104 ON WDW BILL FREYMOND (206)533-9335 63267 PROVIDE FOR FISHERY, ENHANCE WILD STOCKS, MITIGATION
298. SH WIN CL SM CR 17090011 ODFW GEORGE NANDOR (503)630-7210 30000 MITIGATION
299. SH WIN CO'CH SM,EG CR 17070105 NA WDW ULF RASSMUSSEN (206)837-3131 300000 ENHANCE FISHERY
300. SH W IN EL FN Ps 17110017 OA PNPT CHRIS WELLER (206)297-3422 71545 ENHANCE RUN AND FISHERY HATCHERY EVALUATION
301. SH WIN GR GS FN PS 17110013 NA MUCK DENNIS MOORE (206)939-3311 30035 PROVIDE FOR FISHERY, UTILIZE HABITAT
302. SH WIN GS:CH,GR SM PS 17110013 ON MUCK DENNIS MOORE (206)939-3311 31665 PROVIDE FOR FISHERY
303. SH WIN KR BC ON CFSO PAT A. SLANEY (604)228-1158 0ENHANCE PRODUCTION
304. SH WIN MA SM Ps 17110019 ON FWS DAVID ZAJAC (206)753-9460 65000 ENHANCE RUNS (HATCHERY)
305. SH WIN MF FY CR 17090005 ON OOFW DENNIS WISE (503)378-6925 150000 EDUCATION, ENHANCEMENT
306. SH WIN NS FY CR 17090008 ON ODFW DENNIS WISE (503)378-6925 150000 EDUCATION, ENHANCEMENT
307. SH WIN NS SM OC 17090005 ODFW RANDY WINTERS (503)854-3522 220000 MITIGATION
308. SH WIN Pu'QN FN PS 17110014 OA PUT RUSSELL LADLEY (206)593-0254 35778 ENHANCE FISHERIES
309. SH W IN QN,GV SM Ps 17110019 ON SUQ PAUL DORN (206)598-3311 36715 DEVELOP SURPLUS FOR STOCKING
310. SH WIN WI FY PS 17110019 ON WDW TOM JOHNSON (206)765-3979 0RESEARCH
311. SO FN,FY AC ON ADFG NICK DUDIAK (907)235-8191 2000000 ENHANCE FISHERY
312. SO FN AC ON ADFG DAVID LITCHFIELD (907)262-9369 1400000 SUPPLEMENTATION, ENHANCE RUN
313. SO EG AC ON ADFG LORNE WHITE (907)486-4791 6000000 SUPPLEMENTATION, ENHANCE NATURAL RUN
314. SO GU FY AC OA ADFG KEN ROBERSON (907)822-5520 9999999 PROVIDE BROCIDSTOCK AND.ENHANCE FISHERIES
315. SO GU FRY AC ON ADFG KEN ROBERSON (907)822-5520 9999999 ENHANCE FISHERIES
316. SO GU FY AC QA ADFG KEN ROBERSON (907)822-5520 3000000 EVALUATE ENHANCEMENT

Technical Report 90-1

SUPPLEMENTATION OF SALMON AND STEELHEAD STOCKS

WITH HATCHERY FISH:

A SYNTHESIS OF PUBLISHED LITERATURE

C.R. Steward and T.C. Bjornn

Idaho Cooperative Fish and Wildlife Research Unit
University of Idaho, Moscow, Idaho

for

The Office,of Information Transfer
U.S. Fish and Wildlife Service
Fort Collins, Colorado

Dworshak Fisheries Assistance Office
U.S. Fish and Wildlife Service
Ahasaka, Idaho

and

Bonneville Power Administration
Portland, Oregon

1990

Preface

This report was prepared as part of a Bonneville Power Administration (BPA)
funded project to summarize information on supplementation of salmon and
steelhead stocks with hatchery fish, Project No. 88-100. Tom Vogel was BPA
project officer. The primary geographic area of concern was the northwestern
United States with special emphasis on the Columbia River basin.

Three reports were prepared for the BPA project:

1 .Analysis of Salmon and Steelhead Supplementatign: Emohasis on
Unpublished RepQrts and Present Programs, by W.H. Miller, T.C.
Coley, H.L. Burge, and T.T. Kisanuki.
2. Supplementation of Salmon and Steelhead Stocks with HatchM
Fish: A Synthesis of Published Literature, by C.R. Steward and
T.C. Bjornn.

3. Concel2ts for a Model to Evaluate Supplementation of Natural
Salmon and Steelhead $tocks with Hatchery Fish, by T.C. Bjornn
and C.R. Steward.

Reports 2 and 3 were prepared under contract with the Idaho Cooperative
Fish and Wildlife Research Unit at the University of Idaho. The U.S. Fish and
Wildlife Service, Office of Information Transfer helped fund the preparation of
Report2.

The overall objectives of the BPA funded project were to: (1) summarize and
evaluate past and current supplementation of salmon and steelhead, (2)
develop a conceptual model of processes affecting the results of
supplementation, and (3) make recommendations relative to future
supplementation research and needs.

TABLE OF CONTENTS

Page
Preface ................................................................................................ i

Abstract ............................................................................................. ii

Introduction ........................................................................................ 1
Scope of the Review ..................................................................... 1
Goals of Supplementation .............................................................. 1
Some Definitions .......................................................................... 2
Sources of Information .................................................................. 2

Genetic Concerns ................................................ 3
Overview ..................................................................................... 3
Genetic Variation ........................
.................................................. 4
Hatchery Stocks ......................................................................... 16
Source of Broodstock .................................................................. 17
Size of Stock ............................................................................. 17
Selection ................................................................................... 21
Inbreeding ................................................................................. 23
Genetic Impacts on Wild Fish ....................................................... 25
Environmental Effects .................................................................. 32
Recommendations ...................................................................... 33

Ecological Relations ............................................................................ 35
Overview ................................................................................... 35
Competition ............................................................................... 36
Dispersal ................................................................................... 37
Habitat Use ................................................................................ 39
Behavior .................................................................................... 40
Feeding ..................................................................................... 42
Interspecific Competition ............................................................. 43
Growth ..................................................................................... 44
Survival ...................................... ....... 45
Salmon and Steelhead in the Marine Environment ............................ 50
Adults in Freshwater ................................................................... 54
Predation ................................................................................... 56
Fishing Mortality ......................................................................... 61
Disease ..................................................................................... 62

Supplementation Methodology ............................................................. 66
Rearing and Stocking Procedures .................................................. 66
Stocking Densities and Rates ........................................................ 68
Age and Size at Release .............................................................. 69
Time and Location at Release ....................................................... 72

Acknowledgements ............................................................................ 74

References ........................................................................................ 75

Abstract

A synthesis of information related to the supplementation of
salmon and steelhead stocks with hatchery fish was prepared
from a review of published literature. We located few studies
where the effects of supplementation (defined as the use of
hatchery-propagated fish to augment naturally producing stocks)
were directly assessed. However, a large number of related
studies contained useful information. We focused on hatchery x
wild fish interactions and various ecological and methodological
factors that influence them.

Genetic and ecological effects, and changes in productivity of
the native stocks that can result from supplementation remain
largely unmeasured. Releases of hatchery fish into areas
inhabitated by wild stocks can theoretically cause a loss of
genetic variation and adaptedness when wild and hatchery fish
interbreed, and a reduction in stock size resulting from
competitive interactions, increased predation (including fishing),
and the introduction of disease.

For many stocks of salmon and steelhead under consideration
for supplementation, the environments that they migrate through
and in which they must spawn and rear no longer exist in a
pristine state. The environmental changes have created a new
assortment of selective pressures to which the stocks must
respond. Adaptations that formerly enhanced survival and
reproduction may prove to be inadequate or even maladaptive in
the altered habitats. Supplementation, if done improperly, can
be an added burden for the native stocks attempting to adapt to
significant environmental changes.

Based on principles of -population genetics and a limited
number of empirical observations, offspring of matings between
hatchery x wild spawners would be expected to perform less
well on average than pure wild-strain progeny, unless the
hatchery fish are indistinguishable from the wild fish.
Hybridization can break down complex genetic adaptations to
specific environments, and thereby reduce the fitness of
progeny of hatchery x wild matings. Many fisheries geneticists,
therefore, recommend that locally adapted wild fish be used to
start and replenish hatchery broodstocks. Management
practices that promote genetic or phenotypic divergence
between hatchery and wild stocks are discouraged where the
hatchery fish are going to be used to supplement wild stocks of
fish. Gene flow into non-targeted wild stocks due to straying
should also be minimized to maintain and strengthen the
adaptation of stocks to their environment.

The risk of hatchery stocks developing undesirable genetic
characteristics increases when small numbers of closely related
individuals are used as broodstock, when there is purposeful

selection for specific traits, and when outcrossing with wild fish
does not occur routinely. If the traits responsible for poor
performance by hatchery fish have a genetic basis, and hatchery
and wild fish subsequently interbreed, the wild gene pool may
be diluted or otherwise altered. Potentially negative impacts
include the introduction or increase in frequency'of undesirable
alleles, the disruption of locally adapted gene complexes, and
the swamping or homogenization of the indigenous gene pool
through substantial and repeated introductions of hatchery fish.
Even when reproductively isolated from the wild stock, hatchery
fish can act as agents of natural selection if they interaction
with other components of the ecosystem that interact with the
wild fish.

Most stocks of anadromous salmonids used for
supplementation do not appear to have experienced significant
population bottlenecks or inbreeding effects, but there have
been instances of maladaptive selection. An example is the
lower reproductive success observed among naturally spawning
hatchery fish that have been selected for early spawning.
Hatchery fish and their progeny are more likely to encounter
unfavorable conditions, and therefore experience higher natural
mortality, when they spawn earlier than normal in a given
environment.

Once released from the hatchery, stocked salmonids may
interact with their environment, including wild fish, through
competition, predator-prey, parasite-host, and pathologic
relationships. Hatchery and wild fish have similar ecological
requirements and therefore are potential competitors, but the
competitiveness of hatchery fish varies with broodstock,
hatchery history, fish health, and environment. In general, the
longer a fish has been held in the hatchery the less likely it will
be able to compete successfully with wild fish once released. In
the absence of natural stimuli, fish in the hatchery fail to acquire
learned recognition of natural food and predators. Stocked
hatchery fry experience high mortality (as do wild fry), but are
thought to be least impaired by hatchery conditioning. Hatchery
fish stocked as smolts tend to fare well because of reduced
competitive pressures, if they are healthy and migrate to the sea
soon after release.

Whether hatchery fish significantly alter the behavior, growth,
and survival of wild fish remains a controversial subject.
Recently introduced hatchery fish, even those poorly adapted to
the environment, may elicit high levels of activity and stress
among wild fish. Although rare, wild fish may be displaced
under certain circumstances. Hatchery fish may out compete
smaller wild fish, especially if they are stocked as fry or
fingerlings prior to emergence of the wild fish.

Growth and survival of salmon and trout that rear for
extended periods in freshwater is believed to be density-
dependent. The potential for density-dependent effects depends
on the abundance and distribution of hatchery and wild fish
relative to the carrying capacity of the environment. A few
studies have reported lower growth or survival among wild fish
following supplementation.

Adding hatchery salmon and steelhead to drainages can also
affect the status of other taxa, particularly closely related
salmonid species, through competition and predation. Even
when they are not pisciverous, hatchery salmonids may
indirectly increase predation mortality among wild fish. Large
concentrations of hatchery fish may attract larger than normal
numbers of bird, fish, and human predators.

Disease must be considered in an evaluation of
supplementation because it is a major cause of mortality in
hatchery fish and the hatchery fish may serve as disease
vectors. Fish immunogenetic defense systems are often
species- and stock-specific, providing another argument for
using native or closely related salmonid stocks for hatchery
broodstock.

Survival of hatc hery- produced fish in streams depends on the
match of the stocks with environmental conditions, rearing
procedures, the method of stocking, stocking densities, size or
age at release, and time and location of release.
Supplementation managers must consider stocking densities and
schedules in light of program objectives and resources, the
carrying capacity of the ecosystem, the proportion of limiting
resources used by competitors, and the viability (survival and
reproductive success) of hatchery-produced fish.

Introduction

Scope of the Review

Anadromous salmonids are artificially propagated in many parts of the world
to supplement natural production. In the Pacific Northwest, supplementation is
used to maintain commercial and recreational fisheries at acceptable levels and
to rebuild natural stocks that have been weakened by overharvest or habitat
alteration. The effectiveness of supplementation is currently the subject of
much debate and controversy. There have been successes in restoring and
supplementing natural runs of salmonids using hatchery-produced fish (Miller et
al. 1990). However, the general failure of supplementation to achieve
management objectives is evident from the continued decline of wild stocks in
some areas despite, and perhaps partly due to, increases in hatchery
production (Hankin 1982; National Council on Gene Resources 1982; Nelson
and Soule 1987).

The purpose of this report is to provide a synthesis of existing knowledge of
supplementation based on a review of published scientific literature. The
success of supplementation hinges on the post-stocking growth, survival, and
reproduction of hatchery fish, their subsequent integration into existing runs of
wild fish, and the subsequent productivity of the wild-hatchery stock. We
consider, therefore, not only the consequences of superimposing hatchery-
produced fish on wild stocks, but how intrinsic (behavioral, physiological, and
morphological) and extrinsic (hatchery procedures, release strategies and
conditions) factors affect the ecological performance of hatchery fish. We note
where appropriate those observations that appear to lack a firm scientific basis.

Of particular interest with regard to supplementation are the potential genetic
and disease implications of stocking, the degree and types of ecological
interactions (chiefly competition and predation), and the exploitation and
management of mixed-stock fisheries. We discuss stocking parameters and
release strategies that are likely to affect interactions between hatchery and
naturally-produced fish. This review does not provide comment on economic,
political, or social constraints affecting management decisions, even though
these factors have a strong bearing on the direction and success of
supplementation programs.

Emphasis is on anadromous stocks of salmon and steelhead from the Pacific
Northwest. Where possible, we report findings from studies of Columbia and
Snake River salmonid stocks. Investigations of other salmonid species and
geographic locales are discussed if they provide useful information.

Goals of Supplementation

Supplementation is usually undertaken to provide harvestable surpluses of
fish from stocks that may not otherwise naturally produce sufficient fish to
meet the demand from fishermen. Management opportunities range from
rebuilding threatened or endangered wild stocks to bolstering already self-
sufficient natural runs. Hatchery fish used to supplement wild stocks of
salmonids are stocked at egg, fry, fingerling, smolt, and adult life stages.
Although the emphasis and practical details may vary, several goals are
common to most supplementation programs:

1. protect or restore the genetic integrity and productivity of natural
stocks,

2. optimize use of natural habitats (through stocking and management
for optimum spawning escapements), and

3. maximize cost-effectiveness, and

4. provide a harvestable surplus of fish.

The attainment of these goals requires an understanding of the genetic and
ecological consequences of overlapping and possibly interbreeding stocks of
hatchery and wild fish, and a resourcefulness and commitment on the part of
managers in applying this knowledge. Acceptable levels of productivity and
ecosystem stability require management policies that are based on an
understanding of long-term effects and requirements to conserve the gene
resources of natural stocks. Habitat alterations, increased fishing demand
(recreational, commercial, and subsistence), and increased consumption of fish
will amplify the need to consider supplementation as a means of producing
more fish. Better information than is now available will be needed to improve
the effectiveness of supplementation, including the operation of existing and
proposed hatcheries and fisheries management (Davidson et al. 1989).

Some Definitions

In this report, we distinguish salmonids that are naturally produced from
those that are artificially-propagated. Naturally-produced fish are those that
result from natural spawning in streams and are usually of three types: (1)
stocks that have been present in a drainage for several thousand years and are
usually referred to as native or indigenous stocks, (2) stocks that have been
established in vacant areas or restored in depopulated areas by man during the
last 200 years and have developed into self-perpetuating stocks that some may
call feral stocks, and (3) a stock that has been supplemented (regularly or
sporadically) and includes fish of types 2 or 3 above and hatchery fish that
spawn naturally (mating with each other) and produce offspring that spend
their lives in the natural environment. We use the term wild synonymously
with natural to refer to naturally-produced fish without regard to the origin or
genetic history of the parental stock (Hankin 1981; Leider et al. 1984, 1986).

Hatchery fish are those that, regardless of parent stock, have been spawned,
incubated, hatched or reared in a hatchery or other artificial production facility.
The divergence between hatchery and wild stocks that may be supplemented
depends in large part on the origin of the hatchery broodstock and the duration
and history of their captivity.

Sources of Information

References used in this review were obtained through computer-aided
searches of the following literature databases: Biosis, Dissertation Abstracts,
Aquatic Sciences Abstracts, Aquaculture, and Water Resources. Separate
searches were made of FISHLIB - the fisheries literature database maintained by
the Idaho Cooperative Fish and Wildlife Research Unit - and various published
reviews which addressed supplementation issues. The bibliography of this
report contains references that we consider relevant to supplementation, even

if they are not specifically mentioned in the text. With few exceptions, the
references cited in the review and listed in the bibliography are published
articles from journals and symposia.

Worthy of special recognition are several reviews and symposia proceedings
which describe the propagation and stocking of anadromous salmonids. Of the
literature reviews obtained, Kelly et al. (1 988a, b) summarized interactions
between hatchery and wild salmonids, giving particular attention to genetic and
management concerns. Potter et aL (1982) reviewed the effects of stocking
on the population and structural parameters,of native and non-native
salmonids. Kelly et al. (1988) and Potter et al. (1982) discuss management
techniques and criteria for evaluating the success of stocking programs.
Competition and predator-prey interactions are reviewed in Miller (1958) and
Clady (1973). Post-stocking movements of fish are discussed by Cresswell
(1981). Clady (1973) reviews management procedures influencing the return
to the creel of stocked catchable-size rainbow trout.

Prominent among the supplementation literature are several papers
presented at the Symposium on the Role of Fish Culture in Fisheries
Management (R.H. Stroud [editor] 1986). The symposium proceedings contain.
a surfite of information on subjects related to the stocking of cold and
warmwater fish species. We recommend i 't as a companion piece to this
report. Also recommendedare the collection of papers presented in the book
"Population Genetics and Fishery Management," edited by Nils Ryman and Fred
Utter 0 987).

Genetic Concerns

Overview

Genetic resources are important to the well-being of hatchery and wild
salmon and trout stocks and the fisheries they support (National Council on
Gene Resources 1982). Increases in fishing intensity and gear selectivity,
developments in hatchery technology and stocking programs, and habitat
alterations -and losses are all suspected to have affected the genetic
composition of hatchery and wild stocks (Philipp et al. 1986; Nelson and Soule
1987). The effects may be precipitous, as when stocks are overfished (Berst
and Simon 1981), decimated by disease (O'Brien and Evermann 1989), or
otherwise rapidly reduced to a few individuals. Genetic material may also be
lost more gradually through intraspecific hybridization, inbreeding, genetic drift
and artificial selection (Kapuscinski and Jacobson 1987).

Salmonid species consist of numerous, more or less reproductively isolated
subpopulations, that we refer to as stocks, each adapted in varying degrees to
their respective environments (Ihssen et al. 1981; Kapuscinski and Philipp
1988). Genetic variability arising from within- and between-stock differences in
genetic composition is important for two reasons. First, genetic diversity is
necessary if species are to successfully adapt to future natural and man-caused
environmental changes (Thorpe et al. 1981). Preventing the erosion of existing
genetic diversity is essential if stock productivity is to be maintained (Wilkins
1981). Second, genetic diversity is the basis of artificial selection programs
(National Council on Gene Resources 1982; Davidson et al. 1989). Best results

are obtained when the hatchery stock contains a large amount of genetic
variability (Allendorf and Ryman 1987).

A certain amount of selection is inevitable in all aquaculture ventures,
including supplementation. Selection, intentional or otherwise, increases the
risk that hatchery fish will perform poorly under natural conditions. If the
phenotypic traits responsible for the poor performance are heritable, and
hatchery and wild fish subsequently interbreed, the gene pool of the wild stock
may be altered and performance of the resulting population lowered. Hatchery
fish can altering the genetic structure of wild stocks through interbreeding, and
can also alter the natural selection factors through their interaction with other
components of the ecosystem (Krueger and Menzel 1979; Tiedje et al. 1989).
Thus, supplementation has the potential for reducing the long-term fitness and
productivity of existing wild stocks.

In the following sections, we discuss some of the consequences of altering
the genetic makeup of hatchery stocks, and the potential effects of using
hatchery fish to supplement genetically different wild stocks. We also consider
the role of microevolutionary processes (recombination, gene flow, and genetic
drift) in the context of hatchery x wild fish interactions. Potentially harmful
genetic effects include the loss of genetic variability, the breakdown of
adaptive gene combinations, an increase in the frequency of undesirable
"hatcheryn genes, and interspecific hybridization (Allendorf et al. 1987). The
effect of supplementation on wild gene pools had not been measured and
described in the literature we reviewed, but there was there were numerous
warnings that the potential exists for damaging the genetic resources of wild
stocks through poorly planned releases of hatchery fish.

Genetic Variation

Evidence for intraspecies variability in growth and survival rates, food and
habitat preferences, morphology, age and size at maturity, disease resistance,
catchability, and other phenotypic traits is provided in the studies listed in
Table 1. The influence of selective forces in shaping the characteristics of
stocks is evident in the studies listed and underscores the need to consider
stock-specific morphological, life-history, and genetic attributes when choosing
hatchery stocks for supplementation purposes.

Several factors are responsible for the intraspecific structuring of salmonid
stocks. Meteorologic, geologic, and anthropomorphic events affect genetic
differentiation by influencing the distribution of stocks. Natural selection
ensures that genes and genotypes associated with fitness-enhancing traits
increase in relative frequency and thus stocks adapt to local environmental
conditions (Sibly and Calow 1986). The tendency of anadromous salmonids to
home to their natal streams or lakes to spawn helps to maintain and strengthen
stock differences (Davidson 1934; Scheer 1939; Brannon 1967; Ricker 1972;
Barns 1972; Grant et al. 1980; MacLean and Evans 1981).

Because anadromous salmonids encounter diverse habitats during their life
cycle, they experience multiple and possibly conflicting selective pressures.
The degree to which a stock is adapted to its environment is limited by
environmental uncertainty, gene flow (e.g., straying or introductions of

Table 1. Evidence for between-stock variability in adaptive characteristics.

Species Stock Differences References

Pink Odd-year spawning stocks from southern Beacham and Murray
salmon British Columbia varied with respect to egg (1986).
size, egg survival, and alevin and fry size
parameters.

Adults from aerly-spawning northern stocks Beacham and Murray
in British Columbia had higher growth rates (1988).
but were smaller than adults from late-
spawning stocks.

Chum Incubation rates at different water temp- Tallman (1986).
salmon eratures varied between autumn- and
winter-spawning stocks from British Columbia.

Differences in egg size, developmental rates, Beacham and Murray
incubation survival, and alevin and fry size (1987).
were found among seasonally distinct British
Columbia stocks. Head, fin, and caudal peduncle
size of adults increased with river size.

Adult Yukon River salmon matured at a smaller Beacham et al.
size and had smaller fins and caudal peduncles (1988).
than fish from British Columbia stocks. They
were also less fecund, had smaller eggs, and
their embryos took less time to reach hatching
and emergence than did British Columbia stocks.

Sockeye The downstream and upstream migration behavior Brannon (1967).
salmon of recently-emerged fry from inlet- and outlet-
spawning stocks was under genetic control.. ,

Two stocks occur in the same river system in Craig (1985).
in southeast Alaska; fish in the early-spawning
stock entered freshwater in a less advanced
state of sexual maturity, had smaller eggs,
and migrated further upstream than fish from
the late-spawning stock.

When compared to coastal-spawning stocks, fish Beacham and Murray
from interior-spawning stocks exhibited higher (1988).
survival, faster developmental rates, and
larger alevin or fry size at lower incubation
temperatures.

Female investment into egg production was Fleming and Gross
greater in hatchery as opposed to wild spawners (1989).
as a consequence of reduced breading competition.

Table 1. (continued).

Coho Several morphological characters were found to Hjort and Scrack
salmon very significantly among 35 stocks from the (1982).
Pacific Northwest, allowing discrimination of
five major groups of stocks. Hatchery and wild
stocks were differentiated on the basis of
phenotypic traits.

Juveniles from coastal British Columbia streams Taylor and McPhail
had faster burst swimming speeds but less 0 985a, b).
stamina than individuals from interior streams.
They were also more robust-bodied than fish
from inland stocks.

Interpopulation differences in agonistic behavior Roseneu and McPhail
were recorded for juveniles from two tributaries (1987).
to the lower Fraser River (British Columbia).

Female morphological characters associated with Fleming and Gross
swimming and spawning performance varied with (1989).
migration distance to spawning areas and degree
of hatchery domestication.

Stream-rearing juveniles had different body Swain and Holtby
shapes. fin positions, and fin coloration than (1989).
did lake-rearing fish. Aggressive behaviors
were more pronounced among strearri-rearing fish.
Chinook Juveniles of three life history types in a Cad and Healey
salmon British Columbia river exhibited different (1984).
morphologies and allelic frequencies.

Application of a discriminate function developed Winans (1984).
from several morphometric measurements correctly
classified juveniles to their respective stocks
86-90% of the time.

Interpopulation variation in juvenile aggressive Taylor and Larkin
behavior was observed in 10 stocks of stream- (1986).
and ocean-type salmon.

Differences in levels of aggression between Taylor 0 988).
stream- and ocean-type salmon were demon-
strated to be inherited.

Embryos of interior-spawning stocks survived Beacham and Murray
better, developed faster, and attained larger (1988).
size at hatching and emergence at lower incubation
temperatures in comparison to coastal stocks.
Eggs of red-fleshed salmon survived better than
those of white-fleshed salmon when incubated at
higher temperatures.

Table 1. (continued).

Juvenile salmon living in fast water trib- Beacham at al.
utaries of the Yukon River had larger fins (1989).
and more streamlined bodies than fish living
in slower velocity streams.

Atlantic Genetic variation in length and weight after Refstie and Steins
salmon the freshwater phase was measured in 32 (1978).
Norwegian stocks.

Growth in the ocean varied among 37 Norwegian Gunnes and Gjedrem
stocks. (1978).

Differences between stocks in the proportion Naevdal at al.
of grilse (fish which mature after only one (1978).
year in the sea) were observed.

Adaptive, genetically controlled differences Riddell and Leggett
in juvenile body morphology were found between (198 1); Riddell at
fish from different tributaries of the Miramichi al. 0 98 1).
River, Now Brunswick. Timing of downstream
migration also differed significantly.

The lower temperature limit for juvenile growth Jensen and Johnson
was stock-specific for fish from three Norwegian (1986).
streams.

Growth rate and allelic frequency differences Haggberget at al.
were found among presmolts from different (1986).
sections of a large Norwegian river.

Steelhead Juveniles from the Thompson River had greater Tsuyukiand
trout swimming stamina and higher LDH-A (lactate Willis-croft
dehydrogenase) allele
frequencies than (1977).
juveniles from the Vedder River
(British Columbia).

Differences in tolerance to high temperatures Redding and Schreck
between interior and coastal stocks were (1979).
attributed to adaptive variation in IDH (iso-
citrate dehydrogenese) allelic frequencies.

Rainbow Meristic characters and LDH Northcote et al.
trout genotypic frequencies varied in 0 970); Northcote
populations of rainbow trout living above and Kelso 0 98 1).
below a waterfall in two British Columbia
streams. Directional response to water current
differed between two homozygous LDH phenotypes.

Table 1. (continued).

Swimming endurance varied significantly Tsuyuki and Willis-
between two groups of resident rainbow trout croft 0 977).
that were homozygous for alternate LDH alleles.

Cutthroat The direction of migration of cutthroat trout Raleigh and Chapman
trout fry from incubation gravel to rearing areas (1971); Raleigh
following emergence from inlet and outlet (1971); Bowler
spawning streams was genetically determined. (1975).

Brown Survival when exposed to low pH varied among Swartz at al.
trout stocks. (1979).

Freshwater resident and anadromous stocks from Skeels and Naevdal
Norwegian rivers were found to have different (1989).
genetic compositions.

Brook Tolerance to low pH levels varied among gene- Gjedrem (1976).
trout tically distinct stocks.

Lake Retention of swimbladder gas differed between lhssen and Tait
trout between two populations. (1974).

hatchery fish), mutation, and selective advantages for rare alleles (Tiedje et al.
1989).

The genetic basis for the observed phenotypic variability among salmonid
stocks has not been well documented (Allendorf et al. 1987). There is a lack
of standardization in methods used to differentiate genetic and environmental
components of variation for phenotypic traits (Gjedrem 1983; Bailey and
Loudenslager 1986). Correlations between measured genetic makeup and
phenotypic traits tend to be weak and difficult to interpret when environmental
factors predominate in the selection process. Environmentally-mediated
variation in phenotype may override or at least modify the effect of the
genome. Genotype x environment interactions have been'demonstrated for
several traits among salmonids, most notably growth and survival (Aulstad et
al. 1972; Ricker 1972; Ayles 1975; Ayles and Baker 1983; Naevdal 1983;
Iwamoto et al. 1986; Beacham and Murray 1987, 1988; Beacham 1988).

Genetic variation, its distribution among stocks, and the need to use
hatchery fish that are genetically similar to wild stocks are important elements
of supplementation programs. Genetic variation has been positively correlated
with survival for hatchery stocks (Altukhov 1983). Large differences in the
genetic structure of hatchery and wild stocks can potentially lead to lower
survival (Altukhov et al. 1980; Altukhov and Salmenkova 1987) and
undesirable alterations of the wild gene pool (Allendorf and Ryman 1987). A
summary of studies in which the stock structure of salmonid species was
deduced from genetic relationships is provided in Table 2. In several instances,
hatchery stocks have been found to be more closely related to each other than
to local wild stocks (Stahl 1983; Hjort and Schreck 1982; and Taylor 1986).

Table 2. Electrophoretic and DNA-level studies of the population structure of selected anadromous salmonid species within the Pacific
region.

Species Geographical Comments References
area

Pink
salmon
Genetic variability was greater on a temporal Altukhov et al.
rather than a geographic scale. (1983).

Northeast An analysis of 32 populations from Washington Aspinwall
(1974).
Pacific to Alaska indicated genetic differences
between even- and odd-year races.

British Heterogeneity of allelic frequencies was Beacham et al.
Columbia, greater among even- and odd-year broodlines 0 985a).
Washington than among stocks within each broodline.
Significant interpopulation variation was
observed only within the odd-year broodline.

Northwest Bering Sea and Aleutian Island stocks were Gharrett et al.
Alaska genetically distinct from the Kodiak Island (1988).
stock. The genetic profile of Norton Sound
fish more closely resembles Asian stocks than
North American stocks to the southeast.

Chum salmon
Washington, Stocks from north Puget Sound and Georgia Okazaki
British Strait were distinguishable from those of (1981).
Columbia south Puget Sound.

Southern Stocks from four regions could be genetically Beacham
British differentiated; there was significant hetero- et al.
Columbia geneity in allelic frequencies within regions. 0 985a)

Table 2. (continued)

Species Geographical Comments References
area

British differentiated; there was significant hetero- (1985).
Columbia geneity in allelic frequencies within regions.

British Five major regio nal groups of chum salmon were Beacham et al.
Columbia discriminated. (1987).

Sockeye
salmon
Alaska Kasilof River stocks were genetically differ- Grant et al.
entiated from Kenai and Susitna River stocks 0980).
in Alaska. Within-drainage heterogeneity
0 among allelic frequencies was found in all
but the Kasilof River populations.

Identified genetically distinct populations Wilmot and
from the Russian and Karluk River systems in Burger
Alaska. Within-river differences were also (1984).
found among early- and late-spawning stocks.

Coho
salmon
Washington Interdrainage genetic variation indicated Reisenbichler
stock differentiation, but within-drainage and
variation was also high. Phelps 1987.

British Stock separation was possible on a regional Wehrhahn and
Columbia, basis. The mean heterozygosity of southern BC Powell 0 987).
Oregon stocks was an order of magnitude less than
values reported for wild Oregon coho.

Table 2. (continued)

Species Geographical Comments References
area

Chinook
salmon

Alaska Observed inter- and intra-drainage genetic Beacham et al.
differences among populations from the Yukon (1989).
-and Alsek Rivers.

British Allozyme differences among three stocks Carl and
Columbia from the Nanaimo River were related to Healey
juvenile life history. (1984).

Alaska, Stocks from southeast Alaska had genetic Gharrett et al.
British profiles that were intermediate to those (1987).
Columbia of more western and southern stocks.

Oregon, Significant genetic differ 'ences were found Kristiansson
Washington between races of spring and fall chinook in and
the Columbia River. McIntyre
111977).

Washington Interdrainage variation among stocks from Reisenbichler
four coastal drainages was not observed. and
However, differences occured between summer Phelps 0 987).
and fall run fish, between hatchery and wild
stocks, and between year classes.

Pacif ic Identified nine major stock groups distri- Utter et al.
Northwest buted from the Sacramento River northward (1989).
to the Skee na River.

Table 2. (continued)

Species Geographical Comments References
area

Alaska, Mitochondrial DNA analysis of fish from seven Wilson et al.
British stocks corroborated earlier electrophoretic (1987).
Columbia studies.

Rainbow
trout
California High within-stock and low between-stock Berg and Gall
genetic variation was measured in 31 (1988).
coastal populations.

Washington Wild steelhead trout from the Yakima River Campton and
had genetic profiles that were intermediate Johnston
to introduced hatchery stocks and inland (1985).
stocks native to other areas of the Columbia
River basin.

Washington Summer and winter run steelhead from the Chilcote et al.
Kalama River could not be differentiated. (1980).

British Three major regional groups of steelhead Parkinson
Columbia were identified. Significant genetic 11984).
variation frequently occurred among stocks
from adjacent streams.

Midwest Reported genetic divergence of steelhead Krueger and
U. S. A., stocks from ten drainages in the Lake May(l 987).
Ontario Superior watershed and among several streams
in a single large river system. Fall- and
spring-run fish could not be differentiated.

Table 2. (continued)

Species Geographical Comments References
area

British Mitochondrial DNA analysis indicated increas- Wilson et al.
Columbia ing levels of genetic divergence between pop- (1985).
ulations of (1) steelhead, (2) steelhead and
resident rainbow trout, and (3) rainbow and
cutthroat trout.

Significant variation was detected between Wishard et al.
hatchery and wild stocks of resident rainbow (1984).
trout, coastal steelhead stocks and resident
"redband" rainbow trout.

Cutthroat Trout

Washington Anadromous cutthroat trout populations in the Campton and
Puget Sound area differed genetically Utter
on both regional and drainage-wide basis. (1987).

Western Based on an analysis of mitochondrial DNA, Gyllensten and
U.S.A., two subspecies of cutthroat trout could be Wilson (1987).
Sweden differentiated from three stocks of rainbow
trout.

Western Considerable genetic divergence was detected Leary et al.
U. S. A. among coastal, Lahontan, and westslope sub- 11987).
species of cutthroat trout, but little
heterogeneity occurred among Colorado River,
finespotted, greenback, and Yellowstone sub-
species. The first three subspecies were
genetically more similar to resident rainbow
trout than to other cutthroat trout subspecies.

Table 2. (continued)

Species Geographical Comments References
area

Montana Little introgressive hybridization between Marnell et al.
native and introduced cutthroat trout was (1987).
observed among lake populations in Glacier
National Park.

Atlantic
salmon
Newfoundland Anadromous and resident stocks could not be Birt et al.
differentiated from an analysis of mitochon- (1986).
drial DNA patterns.

United The existence of two races of salmon in the Child et al.
Kingdom British Isles was postulated on the basis of (1976).
differences in transferrin allele frequencies.

Northern Analysis revealed considerable genetic Crozier and
Ireland variation in wild stocks within and between Moffett
several river systems. (1989).

Norway Electrophoretic analysis of presmolts indi- Heggberget et
cated that separate stocks exist within the al. 0 986).
River Alta.

United Northern and southern stocks in the UK were Hovey et al.
Kingdom electrophoretically distinct, but populations (1989).
from the north-east and north-west could
not be differentiated.

Eastern Three major groups were identified on the
Canada basis of transferrin allele frequencies: Moller 0 970)

Table 2. (continued)

Species -Geographical Comments References
area

Newfoundland/Labrador, New Brunswick/
Nova Scotia, and Maine.

Baltic Sea Separate stocks were identified within Stahl 0 981;
and between major drainages. 1983).

Based on genetic distance values, major Stahl 0 987).
stock groups correspond to Western Atlantic,
Eastern Atlantic, and Baltic Sea drainages.
Further subdivisions were identified.

Newfoundland Genetically distinct and reproductively Verspoor and
isolated stocks of anadromous and resident Cole 0 988).
Ln salmon coexisted in a lake.

Other investigators have suggested that: (1) most of the total gene diversity
resides within individual stocks (Ryman 1983; Kreuger and May 1987; Hindar
et al. in press; brown trout appear to be the exception - Ferguson 1989), (2)
genetic variation tends to be greater between stocks of different regions than
between stocks within regions (Beacham et al. 1987; Stahl 1987; Verspoor and
Jordan 1989), (3) gene flow may be restricted over very short distances
(Parkinson 1984; Skaala and Naevdal 1989), (4) some stocks have lower
genetic variability than others (Wehrhahn and Powell 1987; Winans 1989; Utter
et al. 1989), and (5) intraspecific gene flow between anadromous and non-
migratory populations is limited (Davidson et al. 1989; Foote et al. 1989).

Genetic differences are not always discerned between stocks from different
drainages, even when phenotypic differences are apparent. The fish may
actually belong to the same stock (Berg and Gall 1988), or they may be
discrete stocks that cannot be differentiated because of sampling problems,
unsuitable genetic markers, limitations of electrophoretic techniques, and
inappropriate statistical analyses (Hallerman and Beckmann 1988). The effect
of electrophoretic proteins on survival and production characteristics is a
subject of considerable debate (Gauldie 1984; Kapuscinski and Jacobson
1987). Discrete stocks probably exist when electrophoretic data and statistical
results indicate clear genetic differences, but the lack of electrophoretically
detectable differences does not preclude the existence of important genetic
differences or status as separate stocks (Riddell et al. 1981).

Effective supplementation requires additional information about the
organization, temporal stability, and ecological significance of genetic variation
within salmonid species (Kapuscinski and Lannan 1986). Continued emphasis
should be placed on obtaining reliable estimates of genetic patterns and
behavior in hatchery and wild stocks. Recently developed techniques using
DNA-level polymorphisms (as opposed to allozyme markers) have been used to
identify intraspecific relationships among salmonids and should improve our
ability to select genetically suitable stocks for supplementation (Hallerman and
Beckmann 1988; Ferris and Berg 1987; Davidson et al. 1989; Hynes et al.
1989).

Hatchery Stocks

The success of supplementation depends on the viability of the hatchery
stocks used to augment natural production. Stock viability can be defined as
the collective fitness, or reproductive capacity, of fish comprising the stock.
From a genetics standpoint, the viability of a stock is affected by evolutionary
forces operating both within and outside the confines of the hatchery.

Hatchery fish that survive and return as adults following their release into
the wild may eventually breed with naturally-spawning fish. The genetic
composition of the wild stock will be altered unless the hatchery stock is
genetically equivalent to the wild fish (Evans and Smith 1986). Genetic
equivalency is affected by the source of hatchery broodstock, by mating and
rearing conditions within the hatchery environment, and by the "culling" effect
of natural selection. Many of the potential genetic effects of supplementation
depend on answers to the following questions (Kincaid 1983). Are some
species or races of salmonids better suited to supplementation than others?
Where will the brood stock be obtained? How many individuals will be used,
both initially and on an ongoing basis, in the breeding program? Will a breeding

program be used which emphasizes specific production traits? What protocols
will be followed to minimize genetic problems?

Source of Broodstock

The source of fish used to start and maintain a hatchery stock is an
important component of supplementation programs. With evidence
accumulating that stocking maladapted fish may be counterproductive (Ricker
1972; Altukhov and Salmenkova 1987), greater consideration has been given
to genetic resources in the design and operation of hatcheries (Heard and
Crone 1976; Reimers 1979).

Broodstocks for new hatcheries are obtained in a variety of ways: transfers
between hatcheries, crosses between broodstocks, selection programs that
emphasize the enhancement of specific traits, and collection of fish from
natural stocks (Kincaid and Berry 1986). Locally adapted fish, when used to
establish and maintain hatchery stocks, are likely to be better for
supplementation than are fish from other populations (Bams 1976;
Reisenbichler 1981; Altukhov and Salmenkova 1987). Smolt-adult return rates
generally decrease with increasing distance from the natal stream for stocked
chinook salmon (Reisenbichler 1988), Atlantic salmon (Ritter 1975), and chum
salmon (Kijima and Fujo 1982).

Some species appear to be less sensitive to transplanting than others,
perhaps a function of the species' dependency on freshwater habitats. Pink
salmon may be more easily supplemented that other species because they are
efficient colonizers of new habitats (Beacham et al. 1985), possess a relatively
uniform or "unspecialized" genetic structure (Ryman 1983; Utter et al. 1980;
Altukhov and Salmenkova 1987), and do not require extensive freshwater
rearing. Because they migrate to the ocean soon after emergence, pink salmon
would presumably receive minimal exposure to selection in the hatchery over
time. Following similar reasoning, "ocean type" populations of chinook salmon,
defined as those producing subyearling smolts (Gilbert 1913; Healey 1983),
may be more tolerant to artificial propagation than would "stream type"
(yearling and older smolts) chinooks. Interior stocks of anadromous salmonids
may be more uniquely adapted to their respective drainages than are coastal
populations due to a tendency for smolting age to increase with shorter and
colder growing seasons (Beacham et al. 1989).

Size of Stock

The number of spawners used to propagate hatchery stocks for
supplementation purposes should be maintained at levels that ensure that most
of the genetic variability is passed from one generation to the next (Wilkins
1981). If appreciable amounts of genetic diversity are lost then the viability of
the hatchery stock may decline, wild stock adaptability may be impaired, and
supplementation goals may be thwarted. These predictions are based on
studies which show that even minimal losses of genetic variability can result in
lower survival and productivity (Kincaid 1983; Allendorf and Ryman 1987).

All finite populations, hatchery and natural, experience some genetic drift
(the direction of change is random but may include permanent losses of rare
alleles) due to natural genetic processes that occur in each generation. The
potential for unwanted genetic change increases whenever too few or too

closely related individuals are chosen for breeding. Genetic material can be
replenished only through mutation or infusions of fish from outside the
hatchery.

The rate at which genetic variability is lost in a hatchery stock depends on
the number, relative reproductive contribution, and genetic similarity of
individuals used for breeding purposes. The proportion of fish that are
heterozygous (having two different alleles at the same locus), within a
population of size N decreases at the rate of 1 - (11 /2N) in each generation,
assuming that each individual spawns successfully. For example, where a large
number (100 or more) of individuals are randomly mated, a reduction of less
than 0.5% of the original genetic variation is expected after one generation
(Figure 1). All else being equal, no more than 5% of the heterozygosity will be
lost in large populations after 10 generations. When 10 fish are used as
broodstock, 5% of the initial heterozygosity is lost in the first generation alone,
and 40% is lost after 10 generations.

Loss of genetic variability is also reflected by the reduction in the mean
number of alleles per locus, expressed as a percentage of the alleles originally
present (allelic diversity; Denniston 1977). The number of alleles expected to
be retained by loci with varying numbers of alleles is a function of breeding
population size (Figure 2). The potential reduction in allelic diversity is most
dramatic (up to 50%) at moderately polymorphic loci when the number of
breeding individuals is small.

Several authors have noted that genetic diversity is low in salmonids
(Ryman 1983; Allendorf and Ryman 1987; Davidson et al. 1989). Examples of
reductions in genetic variability within hatchery stocks, ranging to 20-30%
below wild stock levels, are common for non-anadromous salmonid species and
Atlantic salmon (Table 3). We found few cases of reduced levels of genetic
variability among hatchery stocks of Pacific salmon and steelhead trout.
Busack et al. 0 979) and Thompson (11985) observed levels of genetic variation
in hatchery stocks of cutthroat and rainbow trout that were in some cases
greater than that present in wild stocks.

Because not all fish within a stock have equal reproductive capacities, the
effective population size (Ne - the number of successfully reproducing adults)
rather than the total population size actually determines how much genetic
variation is lost from one generation to the next. Age, fecundity, fertility, sex,
and the degree and magnitude of environmental "accidents" (including those
perpetrated by man) affect the reproductive contribution of each individual
relative to other fish in the stock.

An example of a reduction in the effective population size of a hatchery stock
attributed to spawning technique was given by Gharrett and Shirley (11985).
Milt from adult male pink salmon spawned under identical conditions varied
substantially in its ability to fertilize eggs, the most plausible explanation being
unequal states of maturation among the male subjects. For this reason, the
common practice of simultaneously adding the milt of several males to the @eggs
of a single female cannot be expected to yield progeny with genotypes
proportional to the ratio of males to females used. For species like chinook
salmon and steelhead trout, where large numbers of spawners are frequently
unavailable, the best insurance against unequal potencies among spawners is
to fertilize the eggs of each

Ne= 1000
100 ---- 0.
N =100
go- Ne = 50
(D
Z8()- Ne=1
Z e=5
<70-

Ld 60-N2
Q@e Ne=3
W50-
U
Z40-

30-

020- Ne=1

10-

It 'r-,TIIIII
2 3 4 5 6 7 8 9 10
GENERATION
Figure 1. Rate of loss of genetic variance (heterozygosity) per generation as a
function of effective population size. Taken from Me.ffe (1986).

0.8-

0.4 -

Q2 - 2

5 10 Is 20 25

Figure 2. Proportion of allelic diversity (A) remaining following a single
generation bottleneck in population size of 2, 4, 10, and 25 individuals. Initial
allelic frequencies are assumed to be equal. Modified from Allendorf and
0

@Z@@@2
5

Ryman (11987).

Table 3. A summary of findings from studies which evaluated changes in genetic variability within hatchery populations
of anedromous salmonids. Taken in part from Table S. 1 Allendorf and Ryman (1987).

Species Genetic Attributes References

Coho Although statistically insignificant, the mean Wehrhahn and
salmon heterozygosity of fish from Capilano Hatchery PowellO 987).
was 2.7 times greater than that of wild stocks
from nearby coastal mainland streams of southern
British Columbia.

Chinook The mean haterozygosity and allelic diversity Utter at al.
salmon between 7 hatchery and 6 wild stocks from the (1989).
Oregon coast were not significantly different.

Atlantic Haterozygosity and allelic diversity were reduced Cross and
King (1983)
salmon in a hatchery population five generations removed
from the wild (western Ireland).

In eastern Canada, mean haterozygosity and Verspoor
allelic diversity averaged 26% and 12%, respec- (1988).
tively, lower in fi rst-gans ration hatchery
smolts than in wild stocks.

Hatchery stocks exhibited 20% lower levels of Stahl (1983;
genetic variability than natural populations 1987).
from the Baltic Son.

Mean heterozygosity was not reduced in a hatchery Crozier and
stock in Northern Ireland. Moff Ott
(1989).

Rainbow Inbreeding was suspected as a cause of a reduc- Allendorf and
trout tion in genetic variation. Utter (1979).

Higher levels of mean heterozygosity were Thompson
observed in several hatchery stocks compared to (1985).
wild stocks.

Little loss of genetic variability in two Berg and Gall
hatchery populations was observed. (1988).

Cutthroat Hatchery stock retained about 80% of the mean Allendorf and
trout haterozygosity of the wild founder stock. Phelps
(1980).

Number of polymorphic loci, allelic diversity, Leary at al.
and average haterozygosity were reduced by 57%. (1985).
29%, and 21 %, respectively.

Table 3. (continued)

Species Genetic Attributes References

Brown Proportion of polymorphic loci reduced by up Ryman and
trout to 50%. Stahl
(1980; 1981).

Mean heterozygosity reduced by 33%. Vuorinen
(1984)

Mitochondrial DNA heterozygosity in Swedish Gyllensten
hatchery stocks was 25% of the variability of and Wilson
natural stocks. (1987)

female with the milt from a single male, each fish being used just once.

Effective population sizes that have been recommended to maintain genetic
diversity vary widely (Ryman and Stahl 1980; Allendorf and Phelps 1980;
Hynes et al. 1981; Kreuger et al. 1981; Allendorf and Ryman 1987;
Kapuscinski and Jacobson 1987); the minimum acceptable value probably
depends on the environment and the reproductive biology of the species
(Simon et al. 1986). Theory (Allendorf and Ryman 1987) and empirical
(Verspoor 1988) evidence suggests that little (< 1 %) genetic variability will be
lost in most salmonid species if Ne of the founding population is > 50.
Conservative Ne values recommended by two groups of fish population
geneticists are higher: Kapuscinski and Jacobson (1987) suggest 100 fish,
whereas Allendorf and Ryman (1987) recommend 200 individuals, split evenly
by sex, as a lower population bound for hatchery stocks that are used to
supplement wild stocks.

Reductions in Ne among wild or hybridized hatchery and wild stocks may
derive from individual variation in breeding success and decreases in total
population size. Effective population sizes are less than the observed number
of spawners whenever the sex ratio is unbalanced. However, straying, multiple
age spawning, polygamy, and overlapping generations among wild stocks tend
to maintain Ne and genetic diversity'at higher levels than would be possible for
isolated populations made up of monogamous spawners of uniform age (Helle
1981; Gall 1983; Simon et al. 1986).

Wehrhahn and Powell 0 987) and Winans 0 989)'speculated that the low
levels of genetic diversity which they measured within present day wild stocks
of coho salmon in British Columbia and chinook salmon in the Snake River
drainage resulted from historical population bottlenecks. Plausible explanations
included natural and man-caused reductions in effective population sizes.

Selection

Selective breeding is frequently used in aquaculture to increase the
incidence of one or more desired traits in the hatchery stock (Hynes et al.
1981). Directional or intentional selection may, through the elimination of
specific alleles and genotypes, alter the existing genetic composition and lower

genetic diversity. For reasons stated above, the gene pool of wild stocks can
be altered if they hybridize with genetically distinct or impoverished hatchery
fish.

Salmonid fishes have several characteristics that facilitate artificial selection
in hatcheries: external fertilization, high fecundity, high fertility, short
generation interval, ease of hybridization, moderately high heritability for some
important traits, and large phenotypic variability (Wilkins 1981; Kincaid and
Berry 1986; Parker 1986). These qualities, exploited under diverse aquaculture
programs, have resulted in the development of a large number of hatchery
strains (Busack and Gall 1980; Kincaid 1983). Strain-specific differences have
been documented for several traits, including, but not limited to, egg size and
number, growth rate, body composition, and feed conversion (Kincaid and
Berry 1986).

Genetic protocols and objectives associated with supplementation using
anadromous salmonids differ from conventional fish farming techniques applied
to captive stocks of non-anadromous salmonids (Allendorf and Ryman 1987).
Management goals, rearing and breeding strategies, and criteria used to gauge
the success of the two programs, the one emphasizing ecosystem integrity and
the other production within a closed artificial system, are largely incompatible.
Kapuscinski and Jacobson (1987) and others (Calaprice 1969; Simon 1970;
Purdom 1972) review culture techniques such as selective breeding,
development of inbred lines (i.e., the intentional reduction of heterozygosity),
and heterosis (hybrid vigor due to overdominance and heterozygosity at many
loci) that have been used to improve the production traits of fish used primarily
for aquaculture purposes. Hynes et al. (1981), Simon (1986), Kapuscinski and
Jacobson (1987), and Kapuscinski and Philipp (1988) have summarized key
issues that are relevant to the design and implementation of artificial selection
programs. The general impression imparted by these authors is that selective
breeding will eventually become an effective and important tool in
supplementation efforts, although as recently as 1987 it was the opinion of
Allendorf et al. (1987; p. 19) that "...genetic conservation and (intentional and
inadvertent) selection cannot be achieved simultaneously..." To give but one
example: selective breeding for increased survival of hatchery coho salmon may
have inadvertently contributed to an overall decline in stock fitness (McIntyre et
al. 1988).

More information is needed of life history, ecological, and genetic
characteristics and interactions of hatchery and wild stocks before artificial
selection can be safely and effectively used in supplementation programs.
Kapuscinski and Philipp (1988) recommend a conservative approach involving
manipulation of no more than a few traits, adherence to procedures which
maximize genetic diversity, and careful monitoring and evaluation of post-
selection effects.

Recently developed genetic engineering techniques appear to hold promise
as a means of bestowing desirable traits, such as disease resistance or faster
growth, on hatchery stocks (Kapuscinski and Jacobson 1987). Although the
relative merits and demerits of gene transfers are still unclear (relatively few
structural genes have actually been transferred), genetic engineering may
eventually prove useful in supplementation programs (Davidson et al. 1989).
Potential impacts associated with the introduction of transgenic fish are
discussed by Kapuscinski and Hallerman (1990).

A certain amount of unintentional selection is unavoidable in all fish rearing
operations, including programs and facilities used for supplementation (Hynes
et al. 1981)(Table 4). There is evidence that many of the observed changes
are maladaptive in a natural environment. Selection for early run timing of
returning hatchery spawners is a frequently cited example (Ayerst 1977;
Rosentreter 1977; Smoker 1985; Reisenbichler 1986a; Lbider et al. 1986).
Hatchery managers frequently select for early sexual maturation by taking fish
from the early portion of the returning run of adults. There are practical
benefits to advancing the time of spawning and incubation in the hatchery:
adult mortalities are decreased by reducing the time they are held prior to
spawning, more time is available to grow fish before they are released on a
fixed date or, alternatively, fish can be reared to acceptable sizes for release
earlier in the season (Zaugg et al. 1986; Reisenbichler 1986a).

However, selection for early spawning can have unwelcome results when
hatchery fish attempt to spawn naturally. Early spawners may encounter
temperature and flow conditions that adversely affect intragravel and post-
emergence survival (Cederholm 1984) and they may out compete later
emerging wild fish (Chandler and Bjornn 1988).

Genes coding for traits selected for in the hatchery environment may be part
of larger coadapted gene complexes (Dobzhansky 1970). Selection may
disrupt these systems, leading to reduced genetic variance and population
fitness (Strickberger 1976; Reisenbichler 1984, 1986b; Chilcote et al. 1986).
This type of genetic disturbance, as yet undocumented in hatchery stocks,
.merits future research.

Inbreeding

Inbreeding occurs when spawning pairs of fish are more closely related to
each other than to other individuals in the population (Gall 1987). A potential
cause of loss of genetic variability at both the individual and population level,
inbreeding is promoted by directional and unintentional selection and the use of
small numbers of fish to establish and perpetuate the hatchery stock. Gall
(1987) provides an excellent discussion of the theory of inbreeding as it applies
to hatchery management.

Although inbreeding has long been recognized as a potential problem in
hatcheries, only recently have studies documented its negative effects on
salmonid stocks (Ryman and Stahl 1980; Allendorf and Phelps 1980; Gall
1983). Kincaid (1983) reviewed a number of studies in which inbreeding
depression, defined as an increase in the percentage of individuals that are
homozygotes for recessive deleterious alleles, had a detrimental effect on
fitness measures such as survival, reproductive capacity, physiological
efficiency, and the occurrence of deformities in hatchery stocks. However,
there is little evidence of extensive inbreeding depression among hatchery
stocks of Pacific salmon used for supplementation. Likewise, an infusion of
deleterious alleles into wild stocks via supplementation has not been
demonstrated.

A positive aspect of artificial propagation of hatchery stocks is that problems
associated with selection, inbreeding, and loss. of genetic variation can often be
remedied through careful management. New broodstock can be obtained,
hatchery operations altered, and objectionable selective forces alleviated to

Table 4. Phenotypic traits that were purportedly altered by inadvertent
selection in the hatchery.

Trait References

Body morphology Fleming and Gross (1989).

Deformities Aulstad and Kittlesen (1971);
Kincaid (1976, 1983).

Secondary sexual characters Fleming and Gross (1989).

Sex ratio Altukhov 1981; Doyle (1983).

Age at maturation Rosentreter (1977); Fraser (1981).

Spawning timing Millenbach (1973); Hjort and
and duration Schreck 0 982); Nickelson et al.
(1986); Rosentreter (1977);
Leider et al. 0 986).

Repeat spawning Rosentreter 0 977); Leider et al.
(1986).

Reproduction (fecundity, Aulstad et al. (1972); Fleming and
egg size, etc.) Gross 1989; Gall and Gross (1978);
Kincaid 1976, 1983.

Physiology (temperature Greene (1952); Vincent (1960);
tolerance; stamina, etc.) Hynes et al. (1981).

Stress resistance Vincent 0 960), Barton et al.
(1986); Woodward and Schreck
(1987).

Behavior (docility, Vincent (1960); Moyle (1969);
habitat preference, etc.) Doyle and Talbot (1986).

Catchability Flick and Webster 0 962).

Growth Webster and Flick (1964; 1975, 1976);
Reisenbichler and McIntyre (1977);
Gjerde 1983; Kincaid (1976, 1983).

Survival Greene (1952); Gall (1969); Aulstad
and Kittlesen (1971); Flick and
Webster 0 976); Reisenbichler and
McIntyre 0 977); Chilcote et al. (198 1);
Hynes et al. (1981); Ryman (1982);
Kincaid (1976, 1983); Gjerde (1983).

produce the desired effect in a relatively brief period of time, owing to the short
life cycle and high reproductive rate of the species.

Genetic Impacts on Wild Fish

The genetic impacts of superimposing hatchery fish on natural runs can be
detrimental, benign, or beneficial. Because few studies have measured the
long-term genetic response of wild stocks to supplementation, there exists
more conjecture than fact on this subject. Negative consequences tend to be
stressed in the scientific literature; the disruption of adaptive genes or gene
combinations (coadapted systems; Reisenbichler 1984, 1986b; Chilcote et al.
1986; Taggart and Ferguson 1986), genetic homogenization caused by the
swamping of native gene pools (Temple 1978; Utter et al. 1989; Hindar et al.
in press), and interspecific hybridization (Behnke 1972; Busack and Gall 1981;
Leary et al. 1984; Allendorf and Leary 1988). Genetic risks to wild stocks
increase whenever nonadaptive traits are selected in the hatchery stock, or
genetic variation within the hatchery stock is small relative to the wild stock
(Lannan and Kapuscinski 1984). The extent to which wild stocks are affected
depends on the level of genetic dissimilarity, the reproductive contribution of
hatchery and wild fish, the amount of interbreeding, and the relative fitness of
progeny. Hatchery fish not only are @capable of influencing genetic structure
through interbreeding, they are also likely to effect genetic change through
their interaction with the ecosystem, especially as competitors and predators
Kreuger and Menzel 1979).

Obviously, the introduction of hatchery-produced individuals carrying
maladapted genes is not a productive supplementation strategy. The potential
for unwanted genetic impacts increases when non-local stocks are used to
establish and maintain hatchery stocks. Even small differences in adaptive
traits may cause problems if significant interbreeding occurs. For example,
Bams (11976) found that the accuracy of return by adult pink salmon to native
tributaries was greatest among progeny of resident wild fish, intermediate
among progeny created by crossing non-native and resident fish, and least
among offspring of non-native stock. Unpredictable migrational responses,
including straying, among hatchery fish not only undermines efforts to
supplement wild stocks but may also affect the productivity of non-targeted
stocks in nearby rivers (Calaprice 1969; Ricker 1972; Barns 1976).

Wohlfarth (1986) reviewed six studies in wh ich researchers evaluated the
relative performance of hatchery, wild, and hybrid (hatchery x wild) salmonids.
Performance data from these studies and one by Mason et al. (1967) are
summarized in Table 5. Hybrid progeny of nonanadromous cutthroat and brook
trout had greater viability, in terms of better survival, faster growth, or both
relative to purebred hatchery and wild stocks. In most cases the performance
of pure strain hatchery fish was worse than that of hybrid and wild fish (Mason
et al. 1967).

The two studies reviewed by Wohlfarth (1986) which involved anadromous
species give a clear impression that the long term fitness of interspecific
hybrids may be less than that of purebred wild fish. Reisenbichler and
McIntyre (1977) demonstrated significantly greater survival among offspring of
wild steelhead trout compared with hatchery x wild progeny stocked in natural
streams. Barns (11976) did not observe any survival advantage of native pink
salmon over progeny created by mating fish from separate wild stocks, but

Table 5. A summary of seven studies which evaluated the relative performance of hatchery, wild and hybrid salmonids (from
Woh1farth 1986).

Cutthroat trout (Donaldson et al. 1957)

Background: Parental strain and reciprocal (F - female, M - male) crossbreds of age-0 hatchery (H) and wild (W) cutthroat trout
were stocked into Lake Whatcom, Washington. Mean weight and the numbers of fish caught on opening day of the fishing
season were measured over the next two years.

Individual weight (Q) Percent caught
Number Initial
Stock stocked (Age 0) AQe 1 Age 2 Age 1 Age 2

HFxHM 3006 5.2 98.4 289.3 1.0 0.3
HFxWM 2213 5.4 79.2 256.0 5.6 0.9
WF x HM 4802 5.2 88.5 338.3 6.2 0.4
WF x WM 5890 3.5 66.2 321.3 1.7 0.8

Brook trout (Mason et al. 1967)

Background: A comparison was made of the survival, growth and harvest of age-0 brook trout progeny of hatchery, wild, and
reciprocal (F = female, M = male) hatchery x wild matings that were stocked into five Wisconsin streams. Sources of stock: H
= Osceola hatchery; W-L = hatchery-reared progeny of wild Lawrence Creek stock; W-R = naturally produced progeny of wild
Big Roche-a-Cri stock.

Percent survival Mean length (in.)
Percentage
1 year after 2 years after At time 1 year after caught by
Stock stocking stocking of stocking stocking an-glers

H 38.0 0.4 5.6 9.6 21.0
HFxWM 40.0 2.6 5.1 8.6 15.1
HMxWF 29.9 4.5 4.6 8.5 -
W-L 25.3 9.8 3.6 7.3 4.9
W-R 54.8 10.8 3.3 6.7 6.9

Table 5. (continued)

Brook trout (Flick and Webster 1976)

Background: The survival and growth of purebred stocks of hatchery (New York strain) and wild (Assinica and Temiscamie
strains) brook trout stocked at age-O into Bay Pond, New York, was compared against the performance of progeny from a HF x
WM (Assinica) mating.

Number caught (Mean weight/fish in grams)

Age in years

Number Total Number
Stock stocked 1 2 3 4 5 caught 0/6)

HNY 2995 2 (77) 58(349) 4(422) - - 64 (2.1)
HNY x WA 3050 7(136) 242(572) 38(803) 13(826) 26(844) 326 (10.7)
WA 3126 31 (354) 8(603) 12(826) 8(640) 59 (1.9)
WT 1351 2(122) 30(367) 4(626) 8(640) 5(644) 42 (3.1)

Brook trout (Webster and Flick 1981)

Background: Growth and survival was estimated for pure hatchery (Cortland stock), pure wild (Assinica, Honnedaga, Long Island
Pond, 'and Temiscamie stocks) and hybrid (four wild x hatchery crossbreds) age-O brook trout stocked into Laramie Pond, Now
York. We report weighted means for percent survival, instantaneous growth rate (= In(weight at recovery - In(weight at
stocking))/number of days), and R/S total weight recovered/total weight stocked).

Total Instantaneous
number Percent growth Mean
Stock stocked survival rate R/S

Hatchery 750 41.3 13.5 1.6
Hatchery x Wild 1895 68.1 16.2 3.0
Wild 1747 52.2 17.0 2.5

Table 5. (continued)
Brook trout (Fraser 198 1)

Background: Growth and survival was estimated for pure hatchery (HH = Hill's Lake stock), pure wild (WN = Nippigon; WD
Dickson) and hybrid (HH x WN; HH x WD; and WN x WD crossbreds) brook trout stocked into nine lakes in Algonquin Park,
Ontario. We report weighted means for percent survival, instantaneous growth rate (= In(weight at recovery - In(weight at
stocking)) /number of days), and R/S total weight recovered/total weight stocked).
Total Instantaneous
number Percent Growth Mean
Stock stocked recovery rate Bi-S

H 636 4.5 10.6 0.9
H x WN 264 7.4 16.3 8.0
H x WD 217 7.2 13.4 2.1
WN 63 3.4 12.7 1.1
WD 134 11.8 14.4 6.4
WN x WD 46 9.9 15.8 9.9

Steelhead trout (Reisenbichler and McIntyre 1977)
Co
Background: Measured relative performance of hatchery, hybrid, and wild steelhead trout stocked as embryos and swim-up fry in
a hatchery pond and in four tributaries of Deschutes River, Oregon. H = hatchery fish were progeny of wild steelhead captured
in the Deschutes River and reared in a hatchery; W wild Deschutes River steelhead.
Mean length
Total number Percent Percent of final
stocked survival recovered samr)lg (mm)
Life
Stock stage Stream Pond, Stream Pond Stream Pond Stream Pond

H Egg 24000 - 78.4 - 2.9 - 62 -
Fry 7500 6000 - - 5.5 3.3 63 60

HxW Egg 24000 - 79.5 - 3.3 - 62 -
Fry 7500 6000 - - 5.6 2.6 65 56

W Egg 24000 - 86.1 - 3.7 - 62 -
Fry 7500 6000 - - 7.2 2.4 63 56

Table 5. (continued)
Pink salmon (Bams 1976)

Background: Measured relative performance of purebred donor (wild Kakweiken River stock) and donor x natal (wild Tsolum River
stock) pink salmon released into the Tsolum River. A = green to eyed egg stage, B = eyed egg to fry emergence.

Percent survival Total number recovered

Number
Green to Eyed egg marked and
Stock eyed egg to swim-up released Offshore Rivers

Donor 72.0 96.2 109658 205 45

Donor x natal 84.2 96.3 124792 247 236

suggested that the lower homing accuracy of the hybrid salmon was indicative
of a reduction in overall fitness.

Wolhfarth (1986), however, chose to discount this evidence and concluded,
as Moav et al. (1978) had previously, that heterosis (hybrid vigor) confers
distinct advantages in performance in the natural environment among first
generation interstrain crossbreds. These authors envision a continual
"upgrading" of the genetic resources of wild stocks through repeated
introductions of nonendemic hatchery fish in subsequent generations.

Kapuscinski and Philipp (1988) concluded that more study of the long-term
genetic effects of supplementation is needed before contemplating such a
strategy. One approach would be to label hatchery fish with one or more
genetic marks and then monitor marker frequencies in subsequent generations.
It is dangerous to infer significant changes in individual and stock fitness from
measurements of survival or reproductive success made over brief time
intervals. The assumption that maximizing short-term growth, survival, or
reproductive success is equivalent to maximizing the long-term viability of the
stock may be untenable since additional factors are probably involved on an
evolutionary time scale.

We were unable to locate any published studies in which the fitness of
progeny of hatchery x wild matings was measured over multiple generations
and compared with the fitness of the original hatchery and wild parental
stocks. Chilcote et al. (11986) presented evidence that the survival to smolt age
of naturally spawned progeny of hatchery steelhead trout was approximately
28% that of offspring from wild spawners. Krueger and Menzel (1979) and
Wishard et al. (1984) also documented poor reproductive success among
nonanadromous hatchery brook trout and rainbow trout.

The belief that native fish are always genetically superior to hatchery stocks
has been disputed (Kapuscinski and Lannan 1984). Many stocks of wild fish
have been subjected to intense selection triggered by recent environmental
changes. Some fisheries geneticists (J. Lannan, pers. comm) contend that
fishing, habitat alteration, pollution and other environmental factors may pose a
greater threat to the genetic integrity and persistence of wild stocks than do
current supplementation practices. Large hatchery stocks may be more
capable than small wild stocks of adapting to major environmental changes
such as reduced flows at critical migration periods, pollution, or altered
community structure.

Gene flow from a hatchery stock might have beneficial consequences when
the wild stock has become so small that it has lost or is threatened with the
loss of genetic variation through inbreeding, genetic drift, etc. Under these
circumstances, hybridization of genetically divergent hatchery and local stocks
may constitute the best management option. A potential drawback: genetic
diversity is promoted at the stock level, but is lost at the species level. To
quote Nelson and Soule (11987), "the effect of gene exchange between
subpopulations is to increase the variance within groups, decrease the variance
between groups, and decrease the total variance."

It is debatable whether genetic losses can be reversed once supplementation
is stopped and natural production is restored to adequate levels. High
reproductive rates potentially lead to a greater absolute number of mutations

and recombinations within the population. This, in concert with gene flow,
would theoretically provide favorable alleles which can be selected for and
spread through the .population, thus restoring genetic variability (Lovejoy
1977). However, recent evidence suggests that mutations occur and spread
very slowly through salmonid populations (Chakraborty and Leimar 1987;
Davidson et al. 1989).

An important question, as yet unanswered, concerns the rate and extent to
which fish of hatchery origin naturalize, that is, develop a level of adaptation to
local conditions approaching that of the wild stock. Krueger and May (1987)
noted that nonindigenous brown trout stocked in Lake Superior tributaries in
the early 1900s have segregated into genetically distinct stocks within 80
years. Riggs (1986),argued that naturalization is a complex process which
proceeds at variable rates depending on the selective agents and the genetic,
characteristics of the traits involved. The continual infusion of hatchery fish
into the breeding structure of a wild stock may further complicate and hinder
the process of naturalization. Until more empirical evidence is obtained
(through carefully controlled studies in confined ecological settings), a
conservative tack should be taken, to include maintaining acceptable population
sizes, avoiding unnatural selection, and preserving the genetic purity of wild,
stocks.

Given the potential for genetic destabilization within hatchery stocks and
hybridization between hatchery and wild stocks, why isn't there more
conclusive evidence of genetic damage among wild stocks that is directly
attributable to supplementation? Example's exist of gene flow from hatchery to
wild stocks (e.g.,. Campton and Johnston 1985; Taggart and Ferguson 1986;
Altukhov and Salmenkova 1987; Gyllensten and Wilson 1987) and of genetic
swamping through interspecific hybridization (Behnke 1972; Allendorf and
Leary 1988), but these results do not provide compelling evidence of genetic
harm. More disturbing are the few known cases where hatchery introductions
are thought to have caused the effacement of native gene pools at the
intraspecific level (Altukhov 1981; Campton and Johnston 1985; Gyllensten
and Wilson 1987; Allendorf and Leary 1988). Nonetheless, referring to the
impact of hatchery-produced chinook salmon on wild stocks in the Columbia
River, Utter et al. (1989)'remarked that "hatchery populations established from
(and still reflecting) exotic origins have not noticeably perturbed the allelic
distributions of adjacent populations having indigenous origins."

There is no conclusive evidence to suggest that wild stocks have genetically
benefitted from supplementation. We speculate as to why more definitive
evidence of genetic impact - good or bad - has not been obtained:

- Genetic differences between many hatchery and wild stocks may in
fact be small; hatchery practices may not have appreciably altered
historic genetic compositions in the comparatively short time that
anadromous salmon and trout have been cultured,

- The extent of genetic differences and subsequent introgression has
not been assessed or cannot be discerned using available
technology,

- Hypothesized cause-and-effect relationships involving genetic
changes and stock viability have not been subjected to rigorous
experimentation,

- The effects of gene flow cannot be distinguished from changes
prompted by natural selection or genetic drift,

- Interbreeding and gene flow may not be extensive owing to poor
survival of hatchery fish, strong and rapid selection against unfit
genotypes, and genetic and life history mechanisms that help to
buffer the wild genome against deleterious change.

Environmental Effects

We consider the effects of various environmental factors on genetic
resources because supplementation is often used or proposed as mitigation for
production losses resulting from a variety of causes, and because these causes
continue to influence the demographic and genetic characteristics of stocks.
The need for supplementation in the Columbia River basin has arisen because
of increased mortality rates from overfishing, habitat alteration, and changes in
the biotic community.

Wild stocks are at greater risk of genetic harm when subjected to
environmental stress because more hatchery fish are produced that can interact
with wild fish to compensate for the higher mortality rates in the wild stocks.
If wild spawners breed with and are greatly outnumbered by spawners of
hatchery origin, genetic instability and degradation may ensue. The results of
supplemental stocking, even if hatchery fish are genetically equivalent to the
native stock, may remain unsatisfactory unless the factors responsible for the
decline of wild fish are removed. Appropriately, Ryder et al. (1981) suggest
that if supplementation efforts are to succeed, equal consideration must be
given to restoring degraded ecosystems to some semblance of their former
state.

Environmental perturbation, if severe enough, can result in the partial or
total reproductive failure of a stock, with corresponding genetic effect. Wild
stocks are susceptible to overexploitation in multistock fisheries, especially
when hatchery fish are abundant. If stocks are depleted to low levels, the loss
of genetic variation becomes a major concern (Nelson and Soule 1987). Even
moderate levels of exploitation may result in the selective loss of certain
phenotypes and a concomitant genetic response (Ricker 1958, 1973, 1981;
Larkin 1963; Paulik et al. 1967; Loftus 1976; Ferguson 1989). Traits most
likely to be affected would be those most desirable to the fishery, such as rapid
growth (large fish) and high catchability (Favro et al. 1979; Ricker 1982).
When intense selection is applied over several generations, genetic variability
within and between stocks can be expected to decline, potentially lowering the
viability and commercial value of the affected stocks.

Recommendations

The genetic impacts of supplementation need to be carefully addressed in
fisheries management planning and policy. Management decisions should be
based on a consideration of the underlying stock structure of the species and
an assessment of the genetic risks of proposed actions. It is important that
information on life history, ecological, genetic, and exploitation parameters be
obtained before and after supplementation commences, even if this means
program delays or added costs. Gene flow between hatchery and wild stocks,
ecological interactions, and long-term impacts on natural production should be
evaluated (Kapuscinski and Philipp 1988).

Supplementation is a positive and viable strategy as long as it does not
compromise the genetic integrity of existing wild stocks. Supplementation can
play an important role in restoring and maintaining the genetic resources of wild
stocks. However, where healthy stocks of wild fish exist (including non-target
species), deliberation should be given to maintaining natural production with no
interference from hatchery fish. Native stocks should be preserved for their
genetic, cultural, and aesthetic value (Wagner 1979; Hankin 1981; Martin
1984). Wild stock genomes may be preserved through the establishment of
refuges (Helle 1981) - streams and lakes that are maintained in pristine
condition - and "egg bank" programs (Gjedrem 1981). Cryo- preservation of
newly fertilized eggs, while not yet technically feasible (Parsons and Thorgaard
1985), may someday offer a means of restocking rivers with indigenous strains
(Hindar et al. in press).

Several management approaches to avoiding deleterious genetic impacts
from supplementation programs have been proposed (Reisenbichler 1986b).
One is to minimize the opportunity for hatchery and wild fish to interbreed.
This may be accomplished by keeping the ratio of hatchery to wild spawners
small, by either scaling back hatchery production, increasing the harvest of
hatchery adults, or increasing wild stock escapement through harvest
regulation (Leider et al. 1986; Reisenbi*chler 1986a). Reproductive isolation can
also be promoted through the careful selection of release sites, the use of
sterile fish, and by artificially manipulating the time of spawning of hatchery
fish so that they do not reproduce at the same time as wild fish.

In cases where interbreeding between hatchery and wild fish is desired,
genetic disturbances can be minimized by starting the hatchery stock with
locally-adapted fish, by continually "refreshing" the hatchery stock with wild
genes, and by limiting maladaptive selection in the hatchery environment
(Meffe 1986; Reisenbichler 1986b). The hatchery environment and rearing
protocols can be made to ensure that the hatchery stock remains well adapted
to the natural environment. Semi-natural spawning and rearing channels have
proven useful in this regard.

Nonadaptive mating and rearing practices in the hatchery should be
minimized, even if some production is forgone. Guidelines for mating and
rearing hatchery salmonids consistent with the goals of supplementing wild
stocks and maintaining desirable genetic characters include (Kapuscinski and
Philipp 1988): (1) collecting as many wild spawners as is feasible and selecting
parental pairs that are phenotypically representative of the associated stock,
and (2) selecting a subsample of fertilized eggs for rearing and subsequent
outplanting. Subsampling should be random at each step, and a surplus of

gametes or fish available relative to hatchery rearing space or outplanting
program needs. Hatchery fish should be released at an early age at sizes and
densities that are compatible with those of wild fish and the carrying capacity
of the streams. It is important that hatchery practices which might promote
straying are avoided.

Kreuger et al. (1981) and-Kincaid (1983) have proposed random mating and
systematic line crossing strategies for selecting and maintaining hatchery
stocks to reduce the risk of inbreeding. Inbreeding can be ameliorated and
genetic drift counteracted by maintaining large effective population sizes and
by periodically adding eggs or sperm from wild donor stock. Allendorf and
Ryman (1987) suggest as'a rule of thumb a 10% contribution of wild genes
every second or third generation to introduce new alleles and to minimize
adaptation to the hatchery.

The development and propagation of a hatchery stock intended to
supplement remnant (i.e., endangered or threatened) stocks of wild fish
requires special considerations (Meffe 1986; Kapuscinski and Philipp 1988). It
may not be possible to use fish from an endangered population as source stock
without causing unacceptable reductions in population size and genetic
variation. Closely related stocks or, failing that, fish having similar life history
requirements should be used to rebuild severely depleted stocks. Populations
with high genetic diversity are preferred as donors. Hybridization with the
indigenous stock should initially be carefully controlled so that the hybrid line
can be terminated if results are unsatisfactory. Meffe (1986) provides several
recommendations for managing the long-term genetic resources of endangered
species (Table 6).

In cases of local extinctions and severely altered habitat, Krueger et al.
(1981) suggest crossbreeding fish from a large number of local stocks to create
a single hatchery strain. This strategy would theoretically produce highly
diverse genotypes among the progeny, some of which should be successful
when stocked in the new environment. Marsden et al. (1989) describe a
restoration program for Lake Ontario lake trout populations which aims to
maximize genetic variability through multi-strain stocking.

Current thinking, however, holds that extensive outcrossing may disrupt
coadapted genes that are optimally beneficial when collectively expressed
under conditions to which they are adapted (Reisenbichler 1984, 1986b;
Chilcote et al. 1986; Nelson and Soule 1987). There is a current need for more
information on the role and pervasiveness of coadapted gene complexes in fish.
Until such information is forthcoming, the development of hatchery stocks
through the homogenization of discrete gene pools should probably be
restricted to situations in which the between-stock component of the total
genetic variation is significant (Allendorf et al. 1987) and where significant
gene flow is not expected to occur between the stocked fish and wild
populations (Krueger et al. 1981).

Table 6. Steps that can be taken to minimize adverse genetic impacts when
supplementing endangered wild stocks. Based in part on Table 1 of Meffe
(1986).

1. Monitor genetics of wild and hatchery stocks.

2. Maintain largest feasible effective population size in wild and
hatchery stocks.
Effects:
Reduces the loss of genetic variation.
Reduces the loss of rare alleles.
Reduces the potential for inbreeding.

3. Integrate wild spawners from supplemented stock into hatchery
broodstock.

4. Avoid inbreeding through selective mating.

5. Supplement with non-smolt life history stages.
Eff ects:
Reduces selection for hatchery adapted traits.
Reduces hatchery conditioning (domestication).
Minimizes chances of catastrophic loss of stocks.

6. Do not use hatchery stock to supplement genetically dissimilar wild
stocks.
Effect:
Maintain among-population genetic variability.

Ecological Relations

Overview

Once released from the hatchery, salmonids may interact with their
environment in several ways. Biological interactions include competition,
predator-prey, parasite-host, and pathologic (disease) relations between
salmonids and other organisms. Environmental factors, especially those that
influence system productivity and habitat characteristics, may exert complex
and variable control over each of these processes. In reviewing the effects of
biotic and abiotic factors,on supplementation, we extracted information from a
variety of sources including observations reported for closely related
nonanadromous species.

At the intraspecific level, hatchery and wild fish may: (1) compete directly
for food and space during the freshwater rearing phase, (2) prey on one
another, (3) transmit diseases or parasites to one another, (4) alter migratory
responses, (5) vie for food resources during estuarine and marine phases, (6)
redirect and amplify predation or exploitation, and (7) influence spawning

success through differences in reproductive behavior, timing, and genetic
exchange.

Few studies have been explicitly designed to evaluate the effects of
supplementation on the ecology of wild fish. In most studies, the post-release
behavior, food habits, growth and survival of hatchery fish have been
compared against the normal ecological attributes (as we understand them) of
wild salmonids. Freshwater environments have received the most attention
since fish living in streams, and to a lesser extent lakes, can be readily
observed and because the juvenile life stage is sensitive to compensatory
regulatory mechanisms that are amenable to study (Ricker 1954). Considerably
less is known about competition and predation in saltwater.

Supplementation also affects interspecific relations. High densities of
hatchery fish that are larger than the coexisting species may affect the
competition for resources.

Supplementation may increase the intensity of predation on both hatchery
and wild fish by stimulating aggregative, reproductive, or preferential feeding
responses among non-human predators. The role of man-as-predator is an
important one since differences in fishing mortality among hatchery and wild
stocks will affect the outcome of supplementation. Concerns about the
transmission of disease from hatchery to wild fish and vice versa have
increased coincident with recent outbreaks of infectious diseases in
anadromous fish hatcheries of the Pacific Northwest.

Competition

Competition between individuals of one or more species ensues when the
demand for a resource in the environment exceeds its actual or perceived
availability (Larkin 1956). The potential for intra- and interspecific competition
between hatchery and wild stocks depends on the degree of spatial and
temporal overlap in resource demand and supply. Several authors reported that
hatchery fish, especially those reared in the hatchery for several months, were
less efficient than wild salmonids in exploiting and defending limiting resources,
and therefore at a competitive disadvantage (Clady 1973; Butler 1975; Krueger
and Menzel 1979; Reisenbichler and McIntyre 1977; Vincent 1972, 1975,
1987; Petrosky and Bjornn 1988). Direct competition with wild conspecifics is
often cited as a reason that hatchery fish exhibit reduced growth and survival
in the wild. Conversely, it has been argued that hatchery fish have thrived in
some areas because of reduced competition from declining numbers of wild fish
(Campton and Johnston 1985; Seelbach and Whelan 1988), or because the
hatchery fish had a size or prior residence -advantage (Chandler and Bjornn
1988).

The capacity for hatchery fish to significantly alter the behavior, growth and
survival of wild fish via competition remains a controversial subject.
Supplementation can lower wild stock production if large numbers of hatchery
fish are released (Snow 1974; Thuember 1975; Bjornn 1978; McMullin 1982;
Vincent 1975, 1987; Nickelson et al. 1986; Kennedy and Strange 1986;
Petrosky and Bjornn 1988).

We conclude from the available data that hatchery fish kept in the hatchery
for extended periods before release as pre-smolts may have different food and

habitat preferenda than wild fish, that they will be unlikely to out compete wild
fish, and that post-release growth rates and survival will be low if the wild
stock is at or near carrying capacity in abundance. Hatchery fish put out as
eyed eggs or released as swim-up fry can compete successfully with wild fish,
with the outcome depending on the abundance and size of both the wild and
hatchery fish. Competition from hatchery fish released as smolts could be
minimal if the fish are truly smolts and they are released at the appropriate time
so that they migrate seaward without undue delay. Hatchery steelhead
released as "smoltsm that do not migrate to the sea, for whatever reason, can
pose a competition threat to wild fish. In some years, large numbers of
hatchery steelhead residualize but often have trouble adapting to life in a
stream; many die within months.

Dispersal

Point releases of hatchery-reared presmolts (eggs, fry and parr) and smolts
are a commonly used supplementation technique (Hume and Parkinson 1987).
Limited dispersal or emigration may result in excessive local densities of fish,
underseeded sections of stream between stocking sites, and poor smolting
success (Reisenbichler 1986a). Dispersal patterns of wild and hatchery fish are
often either the cause or the effect of competitive interactions.

Several factors affect the post-stocking movements of hatchery@fish
(Cresswell 1981; Murphy and Kelso 1986): (1) species or strain of fish
stocked, (2) physiological status (i.e., readiness to smolt), (3) age, size, and
numbers of fish stocked, (4) water quality and discharge conditions, (5) habitat
quality and quantity, (7) food availability, and (8) interactions with resident fish.
The influence of many of these variables on the dispersal and subsequent
distribution of hatchery fish is poorly understood.

Hatchery fish stocked as presmolts are expected to move into vacant areas
to rear. Rapid and uniform dispersal following release presumably eases
competitive pressures and optimizes natural production. Although wild fish
seem to disperse within a stream in response to density or habitat availability
(Gerking 1959), the rate and pattern of dispersal of hatchery fish from the point
of release in streams is highly variable. In an Idaho stream where steelhead
trout were stocked as eyed eggs and as buttoned-up fry, dispersion from
stocking sites during the summer increased with increasing stocking densities
(Bjornn 1978). Jenkins (1969) and Hesthagen (1988) reported a positive
relationship between the movement of stocked brown trout and densities of
wild fish. Large groups of hatchery-reared rainbow trout migrated faster and
further from the point of liberation than did smaller groups of fish (Jenkins
1971). Dispersal distance was not related to stocking density of hatchery-
reared steelhead trout fry released into Hastings Creek, British Columbia (Hume
and Parkinson 1987). Petrosky and Bjornn (1988) reported that the proportion
of smolt-size hatchery rainbow trout that dispersed from release sites in an
Idaho stream was not related to stocking levels.

Several environmental facto 'rs have been implicated in the movement of
stocked fish. Hatchery fish are more prone to disperse under conditions of high
or fluctuating flow (Brynildson 1967; Irvine 1986; Reisenbichler 1986a;
Heggenes 1988; Havey 1974), low turbidity (Sigler et al. 1984) and extreme
water temperatures (Cooper 1952; Bjornn 1978). Channel morphology and the
abundance of instrearn cover may influence the post-release movement,

distribution, and density of hatchery presmolts. Bilby and Bisson (11987) cited
the availability of pools and cover as being more important than trophic
conditions in determining the number of hatchery coho salmon fry remaining in
western Washington streams after stocking. Dispersal may be more
pronounced and rapid in streams with poor habitat.

Several researchers have reported that, at least initially, hatchery presmolts
do not disperse readily from the point of release. Hume and Parkinson (1987)
found that most of the steelhead fry released into a coastal British Columbia
stream did not move into nearby vacant areas. Seelbach (1987) and Hillman
and Chapman (1989) reported limited movement of stocked hatchery steelhead
juveniles. In an Idaho stream, most hatchery-reared spring chinook salmon
moved less than 2 km downstream of the point of release (Richards and
Cernera 1989). Limited dispersal has been observed in stocked Atlantic salmon
(Egglishaw and Shackley 1980), steelhead trout (Hume and Parkinson 1987),
anadromous brown trout (Mortensen 1977; Solomon and Templeton 1976),
chum salmon (Shustov et al. 1980) and various non-anadromous species and
strains (Bjornn and Mallet 1964; Clady 1973; Cresswell 1981; Helfrich and
Kendall 1982).

A possible cause of the lack of movement of hatchery salmonids is the
social conditioning they are subjected to at the hatchery. Hatchery fish may be
insensitive to density-dependent migrational stimuli (Symons 1969). Release
methods may also a play a role. For example, dispersal of coho salmon smolts
immediately after stocking was inversely related to the time spent in transit
(Specker and Schreck 1980).

Hatchery presmolts that disperse following release tend to move
downstream (Bilby and Bisson 1987; Mullan and McIntyre 1986; Hillman and
Mullan 1989; Richards and Cernera 1989) under low light intensities (Elliott
1987), but this again appears to vary with species (Moring and Buchanan
1979), developmental stage and condition of the fish (Godin 1982; Thorpe
1982). Upstream movements, generally over a limited distance, have also been
documented (Ruggles 1966; Hearn and Kynard 1986; Hesthagen 1988;
Spaulding et al. 1989). Juvenile chinook salmon and steelhead trout allowed to
emigrate from laboratory streams did so mainly at night (Taylor 1988).

Water temperature and stream flow also affect the directional movements of
stocked salmonids. Exceedingly warm or cold water temperatures may induce
movement into cooler tributaries or into areas containing suitable overwintering
habitat (Bjornn 1978). Cooper (1952) observed trout to move downstream
when stocked at low water temperatures. Some investigators have observed
greater downstream movements of stocked rainbow trout released under high
discharge conditions (Brynildson 1967; Moring and Buchanan 1979), and
greater upstream movement during low flow periods (Clothier 1953). Others,-
however, have reported little or no effect of flow on dispersal patterns (Newell
1957).

Hatchery- produced fish that are undergoing the physiological and behavioral
changes associated with smoltification are likely to emigrate seaward soon
after liberation (Hansen and Jonsson 1985). Timing of the smoltification
process varies some by species and race of fish and is dependent on growth
rate (Zaugg et al. 1986). Hatchery smolts come into contact with wild fish as
they migrate down the larger river systems (Levings and Lauzier 1988), but

generally, the potential for intraspecific competition is minimized when smolts
are stocked if they migrate soon after release. In some anadromous species
(e.g., steelhead trout, Atlantic salmon) smoltification does not take place in all
fish at the same age, even under carefully controlled rearing conditions, and
large numbers of released fish may not be ready to migrate seaward when
released. Although their long-term chances of survival are often small
(Petrosky and Bjornn 1988), "residualized" hatchery fish may interact with wild
fish until they either emigrate or die.

Hatchery-released smolts may induce previous ly,stocked or wild fish to join
them in their seaward migration (Kuehn and Schumacher 1957; Hansen and
Jonsson 1984; Hillman and Mullan. 1989). This response may prove
detrimental to wild fish if they have not yet reached smolt stage or if it
increases their susceptibility to predation. A tendency to emigrate prematurely
has been associated with species-specific behavioral differences and the
presence of instrearn cover (Hillman and Mullan 1989).

Wild fish may be competitively displaced by hatchery fish early in life,
especially when the latter are more numerous, of equal or greater size, and
have taken up residency before wild fry emerge from redds. Naturally-
produced fry normally disperse soon after emergence; smaller fish may be
forced to emigrate under the influence of density- and size-dependent factors
(Chapman 1962; LeCren 1965; Mason and Chapman 1965; Lister and Genoe
1970; Stein et al. 1972; Elliott 1989; Chandler and Bjornn 1988). This may
explain why Hume and Parkinson (1987) found that young steelhead fry (0.2 g)
dispersed up to three times farther than did older hatchery fry (11 g) released
later. Salmonid post-sac fry that emigrate prematurely are not apt to survive in
some situations (Heland 1980a, 1980b; Slaney and Northcote 1974; Mason
1966; Chapman 1962; Gee et al. 1978).

We could not determine from the literature whether wild parr face significant
risk of displacement by introduced hatchery fish. A wide range of outcomes
from wild-hatchery fish interactions has been reported. Wild rainbow trout did
not migrate differentially from heavily stocked sections versus unstocked
sections of an Idaho stream (Petrosky and Bjornn 1989). Similarly,
introductions of hatchery-reared coho salmon or Atlantic salmon did not cause
wild salmonids in the vicinity to emigrate (Hillman and Chapman 1989; Hearn
and Kynard 1986). The distribution of wild steelhead parr in summer was
altered slightly when catchable-size hatchery trout were added to a stream
(Pollard and Bjornn 1973) and a small number of resident brown trout were
displaced by hatchery trout (Bachman 1984). Symons (1969) noted that wild
Atlantic salmon fry dispersed more readily than hatchery fry stocked
simultaneously at the same location. The movement of wild brown trout in a
creek in Montana increased substantially with the introduction of hatchery
rainbow trout. The fraction of brown trout which moved up to 400 m
increased from an average of 19% in non-stocking years to 33% in stocking
years. Brown trout moving over 400 rn increased from 2% to 10% for the
same periods (Vincent 1987).

Habitat Use

The use of habitat by hatchery trout and salmon is often indistinguishable
from that of wild fish, particularly when the hatchery fish are stocked as eggs,
f ry, or young parr (Bjornn - 1978), but may differ f rom that of wild f ish if the

hatchery fish have been kept in the hatchery for an extended period.
Divergence in habitat use may be caused by behavioral conditioning that occurs
in the hatchery and by competition-related interactions after release. Pollard
and Bjornn (11973) reported that stocked rainbow trout congregated in deeper
water than did native steelhead trout in an Idaho river, similar to the
observations of Hillman and Chapman (1989), who found the hatchery
rainbows in pools and the wild steelhead in riffles, runs, and cascades. In both
studies, hatchery and wild rainbow trout were spatially segregated.

Petrosky and Bjornn (1988), after introducing catchable-size hatchery
rainbows into two Idaho streams, concluded that hatchery fish did not use the
same habitats as native cutthroat and wild rainbow trout. Bachman (1984)
observed that hatchery brown trout, on average, used less energy-efficient
foraging sites than did wild brown trout.

Hatchery-reared fish often fail to seek cover after release (Raney and
Lachner 1942; Vincent 1960). In stream tank studies, Dickson and
MacCrimmon (1982) and Sosiak (1978, 1982) observed that hatchery Atlantic
salmon parr occupied positions further from the substratum than did wild
salmon. The higher stationing probably reflects the joint effects of hatchery
conditioning and competition with resident fish. Since wild Atlantic salmon
normally remain close to the streambed (Gibson 1973), and inasmuch that this
behavior has energy and predation cost-minimization value (Fenderson et al.
1968), we infer that such shifts in habitat use are detrimental to hatchery-
reared fish.

In the cases where hatchery fish are stocked as eggs, fry, or young parr,
we would expect a high degree of habitat use overlap between wild and
hatchery fish and significant competition for resources. Stocked steelhead fry
competed effectively with wild rainbow trout in a productive Idaho stream, and
the population in the stream was changed from wild rainbow trout to mainly
juvenile steelhead after a few years of fry stocking (Bjornn 1978).

Behavior

The success of supplemention using presmolts hinges on the ability of the
hatchery fish to behave in a way that will allow them to grow and survive
following release. The differences in behavior between wild and hatchery fish
appear to be minimal early-in life and increase with length of time spent in the
hatchery. Differences in the behavior of hatchery and wild fish which seem to
affect competitive interactions, habitat use, growth, and survival have been
found (Sosiak et al. 1979; Dickson and MacCrimmon 1982). Ersbak and Haase
(1983) have identified several behaviors that were successful in the hatchery
rearing environment, but maladaptive in the wild: (1) a lack of wariness and a
surface or mid-water orientation (Vincent 1960; Moyle 1969; Sosiak et al.
1979; Legault and Lalancette 1985; Dickson and MacCrimmon 1982), (2) an
inability to form social hierarchies or hold positions in the natural stream
environment (Chapman 1966; Bachman 1984), (3) excessive activity (Moyle
1969), and (4) high levels of aggression (Fenderson et al. 1968). To this list
may be added sub-optimal foraging strategies (see the section on Feeding
below). Some of these behavioral differences may be genetically based, but
are more likely environmentally induced (Suboski and Templeton 1989).

Unusual physiological and behavioral characteristics of hatchery fish may
predispose them, as Fenderson et al. (1968) remarked, to "loss of feeding time,
excessive use of energy, and increased exposure to predators." Bachman
0 984) came to much the same conclusion, suggesting that excessive energy
expenditures were primarily responsible for the high mortality of hatchery
brown trout he observed in a Pennsylvania stream. Petrosky's (1984; p. 86)
description of the behavior of hatchery rainbow trout and resident wild
cutthroat trout in a natural stream is instructive:

"Upon release, hatchery rainbow trout formed aggregations in
generally deeper and swifter water in midstream than that preferred
by cutthroat trout ... Most hatchery trout remained in groups
segregated from wild cutthroat trout. These aggregates had no
apparent hierarchy. During infrequent feeding, several group
members pursued and fought over single items drifting past the
group ... Hatchery rainbow trout charged, drove, and nipped each
other proportionately more often than wild cutthroat trout."

Hatchery salmonids are apparently less adept at conserving energy, and
they do not perform as well as wild fish in stamina tests (Vincent 1960;
Reimers 1956; Miller 1955, 1958; Green 1964; Barns 1967; Cresswell and
Williams 1983). Horak (1972), working with nonanadromous rainbow trout,
found hatchery fish had more stamina than wild fish. Hatchery-reared fish
examined by Phillips et al. (1957) and Green (1964) had more fat and poorer
muscle tone than wild fish. Nutritional deficiencies, notably imbalances in fatty
acid composition, were suggested as a cause of reduced viability among
hatchery fish by Bolgova et al. (1977).

The high level of aggressive behavior observed among hatchery fish
following stocking (Fenderson et al. 1968; Moyle 1969; Fenderson and
Carpenter 1971; McLaren 1979; Dickson and MacCrimmon 1982; Swain and
Riddell 1990) may be misleading, and one must be careful in concluding that
hatchery fish are more aggressive than wild fish. Aggressive encounters
between wild fish begin immediately after emergence and occur as needed to
establish and maintain dominance hierarchies or territories. Natural aggressive
tendencies of salmon and trout may be suppressed in the hatchery, and the
high level of aggression observed following release should not be unexpected
when the fish are placed in an environment where there is diversity of habitat
and food for which to compete. Doyle and Talbot (1986), found that selection
for rapid growth in the hatchery did not result in higher levels of aggression;
using game theory analysis, the authors predicted that hatchery selection may
actually favor more docile fish. Elson (1975) hypothesized that newly stocked
hatchery juveniles would be less aggressive than resident wild fish and
therefore easily displaced. Swain and Riddell (1990) provide data which
suggest that differences in aggressiveness may be genetic. These authors
argue that hatchery juveniles may aggressively displace resident wild fish, only
to suffer high predation mortality as a result of their conspicuous behavior.
This hypothesis has yet to be tested.

Competitive bouts between hatchery and wild fish were usually more
inten'se or prolonged than similar encounters between wild individuals
(Fenderson et al. 1968; Dickson and MacCrimmon 1982). Excessive visual and
social contact between "unfamiliar" hatchery and wild fish may elicit high levels
of excitement and aggression in both groups (Li and Brocksen 1977). The

sudden change in environment probably contributes to the social disorientation
of recently released hatchery fish.

From direct underwater observations, Shustov et al. (1981) concluded that
2 to 4 weeks are necessary before hatchery-produced juvenile Atlantic salmon
display normal territorial behavior in the wild. Fenderson et al. (11968), on the
other hand, found that hatchery Atlantic salmon parr attained social dominance
over wild salmon parr in aquaria within one or two days. We suspect that the
relatively poor performance of the wild salmon in the latter study was caused
by the combined stresses of electrofishing, handling and subsequent
confinement in unnatural surroundings. Woodward and Strange (1987)
reported that wild rainbow trout are more susceptible to stress than are
hatchery trout. Bachman (1984) found that hatchery brown trout, although
initially achieving social parity with wild fish, did not successfully penetrate the
long-term social fabric of the wild stock.

Feeding

The foraging success of hatchery fish following their release into the wild
depends on their experiences, feeding opportunities, and habitat quality.
Dietary overlap and competition between hatchery and wild salmonids is
influenced by differences in microhabitat use, differences in foraging tactics
and abilities, and size-dependent differences in prey selection. As far as we
know, the diet or feeding habits of wild fish are unaffected by the introduction
of hatchery fish. Theoretically, the amount of food available to individual fish
should decrease with supplementation, but that depends on how well the
hatchery fish adapt to feeding in the natural environment.

Salmonids have little opportunity to capture live prey while confined in
hatchery raceways and ponds. Nevertheless, hatchery-reared fish appear
capable of switching to a natural diet following release (Lord 1934; Raney and
Lachner 1942; Jenkins et al. 1970; Ware 1971; Bryan 1973; Ringler 1979;
Vinyard et al. 1982; Paszkowski and Olla 1985a, 1985b). Salmonids
previously fed only hatchery pellets soon selected wild prey over artificial food
when offered a choice (Bryan 1973; Paszkowski and Olla 1985b). In light of
these results, suggestions by Kanid'yev (1970) and Suboski and Templeton
(11989) to train hatchery fish to recognize natural food prior to release appear to
be inappropriate.

If hatchery fish are able to switch to natural food items, why is malnutrition
and starvation so often the fate of some hatchery fish in the wild Klak 1941;
Miller 1951; Reimers 1963; Ersbak and Haase 1983; Bachman 1984)? Again,
a distinction must be made between hatchery fish released early in life (eggs,
fry, young pard and those that are reared for an extented period in a hatchery.
The former usually adapt to feeding in the wild and grow naturally (Bjornn
1978), while the latter may have difficulty adapting fully to life in a stream,
especially in relatively infertile streams where food likely limits production of
fish. Hatchery fish that had spent significant time in the hatchery appear to be
inefficient foragers that exist on suboptimal natural diets (Klak 1941; Reimers
1963; Fenderson et al. 1968; Moyle 1969; Elliot 1975; Sosiak et al. 1979;
Shustov et al. 1981; Bachman 1984; Marnell 1986). Ersbak and Haase (1983)
suggested that hatchery trout may have greater difficulty in detecting and
exploiting increasing densities of certain forage items than do wild trout.

Hatchery juvenile Atlantic salmon examined 1-3 months after release ate a less
varied diet than did wild fish (Sosiak et al. 1979).

Differences in stream microhabitats occupied by hatchery and wild
salmonids may account for dietary differences during presmolt stages.
Hatchery-reared juvenile Atlantic salmon assume positions higher in the stream
water column than do wild salmon (Sosiak 1978), reflecting a conditioned
response to feed at the surface (Peterson 1973). A comparison of the diets of
hatchery fingerling rainbow trout with wild rainbow, brook and brown trout in
the Salmon River of New York by Johnson (1981) revealed considerable dietary
overlap. Interestingly, the types of food eaten by hatchery rainbow trout more
closely resembled the diets of resident brook and brown trout than wild
rainbow trout.

Interspecific Competition

Interspecific competition within the context of supplementation has not
received much attention even though there are compelling reasons to consider
interactions between hatchery fish and other species of fish living in the
streams to be supplemented. Resident fish may affect the survival of the
hatchery fish, and, conversely, hatchery fish may affect the abundance or
productivity of coexisting species.

We presented evidence earlier that hatchery fish frequently segregate
spatially from wild conspecifics in streams. It is not known whether this
segregation is a product of intraspecific competition or hatchery conditioning,
but the use of different habitats by the hatchery fish may explain why the diet
of hatchery rainbow trout resembled that of wild brook and brown trout more
.that of wild rainbow trout in a New York stream (Johnson 1981).

Many of the behavioral anomalies of hatchery fish described in the sections
on intraspecific interactions are also liable to affect interactions with other
species. High densities of hatchery fish may suppress the normal behavior of
other species (Stringer 1952, cited by Fraser 1968).

Size differences between hatchery trout or salmon and other species of fish
affect competitive interactions and the partitioning of stream resources (Lister
and Genoe 1970; Everest and Chapman 1972; Griffith 1972; Allee 1982;
Cunjak and Green 1984). Petrosky (11984) reported that hatchery rainbow
trout occasionally challenged wild cutthroat trout for permanent feeding
.stations after stocking in an Idaho stream. Only a few hatchery fish - always
larger individuals - were successfully integrated into the size dominance
hierarchy of the wild cutthroat trout population.

The potential for interspecific competition depends on the relative
abundance of the stocked and resident fish species and the degree of niche
overlap between them. Growth and survival are affected when the stream is
"overseeded" and access to limiting shared resources is regulated by
competition. By experimentally manipulating the relative densities of steelhead
trout and coho salmon fry, Fraser (1968) observed inters lpecif ic effects on
growth and mortality at high stocking densities (14.22 fish/m2). Likewise,
LeCren (1965) found that the survival of stocked Atlantic salmon was inversely
proportional to the total density of brown trout and Atlantic salmon present;
the survival of resident brown trout did not vary with stocking level. Kennedy

and Strange (11980, 1986), on the other hand, observed a large decline in
brown trout fry populations in lagged response to repeated introductions of
Atlantic salmon fry. Reductions in the growth and survival of trout fry were
attributed to interspecific competition with older (age-1) salmon that had been
stocked as fry. Reciprocal effects were also noted: stocked salmon fry
survived better and grew faster when older age classes of trout had been
removed. Interestingly, competition between salmon and trout fry did not
appear to affect the survival of either species. In an Idaho stream, annual
stocking of steelhead fry resulted in a substantial decrease in the abundance of
wild (non-anadromous) rainbow trout, but had little effect on brook trout that
were present (Bjornn 1978). In the same stream, removal of all fish larger that
15 cm resulted in a doubling of the survival rate during the first summer of life
for stocked steelhead fry (Horner 1978).

Growth

When densities of presmolts are increased through supplementation, the
result is usually a decrease in the amount of food available per individual (Colby
et al. 1972). Freshwater growth among salmonids is apparently density-
dependent (McFadden 1968; LeCren 1972; Mortensen 1977; Bjornn 1978) so
we should expect growth rates of wild fish to decline following stocking if the
hatchery fish begin feeding on natural foods and the abundance of fish is near
carrying capacity of the stream. Unfortunately, we could find few instances
where the growth rates of wild fish were measured coincidence with the
stocking of hatchery fish. Vincent (1987) measured a decline in the annual
growth rates of several age classes of wild brown trout after catchable-size
rainbow trout were stocked in some Montana streams. In a productive Idaho
stream, Petrosky and Bjornn (1988) reported that growth of wild rainbow trout
was not reduced when catchable-size rainbow trout were stocked at a rate that
doubled the density.

In other studies, wild salmonids reportedly grew more rapidly than hatchery
fish in natural environments (Needham and Slater 1943), but more slowly in
hatchery environments (Reisenbichler and McIntyre 1977). Nielson et al.
(11956) reported that the hatchery-reared trout he studied grew as well as
native trout in the wild. Subyearling hatchery steelhead stocked at different
densities in a Vermont stream showed little evidence of compensatory growth
(Wentworth and LaBar 1984). In an Idaho stream stocked with varying
densities of steelhead fry and chinook salmon parr, the steelhead were 10 mm
or more shorter at the end of summer when the highest densities of fish were
present (1.5 fish/m2) compared to their length at lower densities (Bjornn 1978).
Hume and Parkinson (1987) observed a weak (but significant) inverse
correlation between the density and growth of outplanted steelhead fry and
yearlings after one to two months of stream residence. Similarly, Egglishaw
and Shackley 0 980) and Egglishaw 0 984) established that the growth of
stocked underyearling Atlantic salmon was inversely related to the density of
age-1 + salmon.

It is not uncommon for catchable-size hatchery trout and residualized
steelhead smolts to lose weight during the weeks or months following stocking
(Miller 1953, 1958; Ersbak and Haase 1983) and many do not survive to
migrate seaward the following spring. In two studies where the growth of
subyearling chinook salmon was monitored during the summer after stocking,
the fish lost weight in one stream, and more than doubled their weight in the

other. Age-O chinook salmon stocked in an infertile stream in late July of two
years at mean total lengths of 71 and 75 mm and weights of 4.4 and 5.4 g,
lost about 20% of their weight during the remainder of the summer (Sekulich
1980). Smaller chinook salmon (55-60 mm in length) stocked in a productive
stream in June increased in length and more than doubled their weight during
the summer (Bjornn 1978). Negative or reduced growth experienced by
hatchery fish in some situations is a consequence of inadequate food supplies
in some cases, such as in infertile streams, but their inability to feed as
effectively as wild fish because of conditioning while in the hatchery probably
is a major factor that intensifies the longer a fish is kept in the hatchery.
Starvation and the metabolic costs of competing unsuccessfully for access to
food (Doyle and Talbot 1986; Miller 1952, 1958; Bachman 1984) can cause to
severe weight loss in the hatchery fish that ultimately leads to mortality
(Reimers 1963).

Salmon and steelhead reared to the smolt stage and then released may grow
a significant amount while migrating to the ocean if the rivers are relatively
clear, but may have to rely on body reserves if the rivers are turbid and food
items are not visible. Smolts that must migrate long distances from the upper
reaches of the Columbia River drainage, for example, probably have enough
energy reserves unless they are delayed migrating through the reservoirs and
are unable to find food.

Survival

Survival of hatchery fish following stocking is a function of several factors
,including stream productivity, habitat quality, the physical condition of hatchery
fish and their ability to acclimatize to stream conditions, the size and stocking
density of hatchery relative to wild fish, depredation and disease, and stocking
practices and techniques (e.g., season, rate, and location) (Murphy and Kelso
1986; Schuck 1948; Nielson et al. 1957; Clady 1973).

The high post-stocking mortality that is characteristic of transplanted
anadromous (Table 7) and non-anadromous salmonids has been associated with
several unfavorable conditions. Physiological stress due to crowded rearing
conditions, transportation, handling, increased social interactions, and novel
environmental demands probably increases the mortality of stream-stocked
salmonids (Mason and Chapman 1965; Specker and Schreck 1980). Excessive
levels of stress can deplete energy reserves and upset osmoregulatory and
metabolic function (Wedemeyer 1972; Selye 1973; Mazeaud et al. 1977;
Strange et al. 1977). Miller (1958) found that hatchery rainbow trout
accumulated high levels of blood lactate levels following stocking and
suggested that socially-instigated stress may have contributed to their poor
survival.

Lack of exercise in the hatchery environment has been suggested as a
cause of lowered vitality and a concomitant reduction in survival (Schuck
1948). A rapid decline in the condition of hatchery trout as energy stores are
depleted has been cited as a possible cause of generally poor survival in
streams (Klak 1941; Miller 1952, 1954, 1958; Reimers 1963; Ersbak and
Haase 1983). Miller (1951) found that 30% of age 3+ and 50% of age 2+
hatchery-reared cutthroat trout died during the first 40 d after release in
streams, apparently from exhaustion and starvation. The survival of fed coho

Table 7. Estimates of post-stocking mortality reported for hatchery-produced Atlantic salmon and steelhead trout. Modified from Bley and
Moring (1986).

Life Percent
Species Location stage survival Reference

Atlantic Scotland Egg to fry 11.1-14.8 Egglishaw and Shackley (1980)
salmon Fry to 0+ 9.4-31.0
0 + to 1 + 51 (22-88)

Scotland Egg to smolt 1.0-3.0 Egglishaw and Shackley (1971)

N. Ireland Green egg 1.4 Kennedy and Strange (198 1
to f ry
N. Ireland Eyed egg 6.8-37.1 Kennedy and Strange (1980, 1984)
to f ry
Fry to 0 + 16.7 Kennedy and Strange (1984)
..0+ to 1 + 14.3-31.7

Ireland Smolt to adult 12.7-4.4 Piggins (1980)

Scotland Fry to 0 + 1.3-23.3 Mills 0 969)

Scotland Fry to smolt 2.4-3.1 Mills 0 964)

Scotland Egg to 0 + 1.7-2.0 Shearer 111961)
Egg to 1 + 0.08-0.46

United Fry to 0 + 1.7-8.8 Stewart (1963)
Kingdom Fry to 1 + 3.6

United Fry to smolt 0.25-1.7 Harris 0 973)
Kingdom Smolt to adult 2.1-3.8

Table 7. Icontinued)

Life Percent
Species Location stage survival Reference

France Eyed egg 50-80 Brunet (1980)
to fry
0+ to I + up to 90

Sweden Smolt to adult 0.4-13.1 Wendt and Saunders 11973)

Sweden Smolt to adult 12.5 Larsson (1984)

Ontario Fry to 0+ 12.7 (10.7-14.6) MacCrimmon 11954)
Fry to 1 + 9.2 (9.0-9.2)
Fry to smolt 3.0

Quebec Fry to age-0 + 5-72 Cote and Pomerleau (1985)
%J 0+ to 1 + 1 -31

New Fry to 1 + 8.0-12.0 Dickson and MacCrimmon 0 982)
Brunswick

Maine Smolt to adult 0.7-1.4 Baum (1983)

Steelhead
.trout
California Egg to 30-80 Shapovalov J 1937).
emergence

Oregon Egg to 18-99 Phillips et al. (11975).
emergence

(daho Egg to 40-95 Bjornn (1978).
emergence

Table 7. (continued)

Lif e Percent
Species Location stage survival Reference

California Emergence to: Burns 0 97 1).
age-0 27
age-1 + 56

Idaho Emergence to: Bjornn (1978).
age-0 10-20
age- 1 6-41
smolt 0.4-3.8

California Fingerling 2 Hallock et al. 0 961).
to adult

oo
California Smolt to 2.1-18 Shapovalov (1967)
adult

Oregon Smolt to 0-10 Wagner (1963).
adult

Oregon Smolt to 3.9-10.9 Wagner (1968).
adult

Oregon Smolt to 1.7-7.0 Wagner 111969).
adult

British Smolt to 5 Hume and Parkinson
Columbia adult (1988).

Coho salmon

Western Fry (spring 13-34 Bilby and Bisson 0 987).
Washington to autumn)

salmon fry was greater than unfed fry following stocking in Puget Sound
streams (T. Flint, pers. comm., cited by Wunderlich 1982).

The post-stocking survival of hatchery presmolts and smolts is sensitive to
the number of fish stocked (Wentworth and LaBar 1984; Hume and Parkinson
1987) and local densities of prior residents (Kennedy and Strange 1986). In a
Washington study (Royal .1972), a d e nsity-de pendent relation was found
between steelhead smolt production and adult returns for hatchery fish that
were forced to migrate long distances to the ocean. A freshwater mortality
agent was implicated (but never identified) when the survival rates of fish from
coastal hatcheries did not show similar trends. Although some biologists
consider density-dependent mortality during freshwater migration to be
negligible (Lichatowich and McIntyre 1987), supplementation managers should
consider the potential for unwanted density-dependent interactions between
hatchery and wild smolts.

Competition-induced shifts in habitat selection by hatchery trout may reduce
their chances of survival. High mortality of hatchery-reared salmonids has been
attributed to their selection of microhabitats which are not conducive to
survival (Vincent 1960; Dickson and MacCrimmon 1982; Petrosky and Bjornn
1988). Competition for preferred microhabitats can be dampened and feeding
opportunities increased by scattering fish in underseeded, high quality rearing
areas. Bilby and Bisson 0 987) concluded that the survival of hatchery fish
was enhanced by the presence of pools and instrearn cover. Greater structural
heterogeneity would reduce visual contact with potential competitors and
predators, and it might temper the effect of floods on stocked fish (Odonera
and Ueno 1961).

Overwinter survival of hatchery fish can be very low, often nil (Needham
and Slater 1944; Heimer et al. 1985; Petrosky 1984), although Adelman and
Bingham (1955) found little or no difference between hatchery and native
brook trout in their ability to survive the winter months. Overwinter survival
was highest for fall-stocked hatchery brook, brown and rainbow trout in
streams where surface ice was rare and cover was present (Brynildson and
Christenson 1961). Mason et al. (1967) noted higher overwinter survival of
hatchery fish relative to wild fish in 3 of 5 streams, which they attributed to
the larger size and good condition of hatchery fish going into winter. Reimers
(1963) discusses the nutritional status of stocked hatchery trout as it relates to
overwinter survival.

The survival to returning adult of hatchery-reared chinook salmon
(Reisenbichler et al. 1982), coho salmon (Salo and Bayliff 1958; Nickelson et
al. 1986) and steelhead trout (Wagner et al. 1963) was positively related to
their size at release. The liberation of large presmolts has at least two important
consequences with regard to their competitive abilities and subsequent
survival. First, a large average size at release may reduce the length of time
spent in the stream, thereby increasing chances for survival to smolt stage.
Second, hatchery fish, if larger than wild cohabitants, are more likely to be
successful in agonistic encounters. Flick and Webster (1964) and Mason et al
0 967) were able to demonstrate higher survival among hatchery salmonids
when they possessed a size and presumably a competitive advantage over wild
residents.

As reported by Nickelson et al. (1986), juvenile hatchery coho salmon used
to supplement wild stocks in Oregon streams averaged half again as large as
resident wild coho (62 versus 39 mm in length) when released in late spring.
Hatchery fish were larger due to earlier emergence and accelerated growth in
hatchery facilities. Outplanting hatchery coho salmon presmolts increased by
41 % the density of juveniles rearing in pools (the preferred habitat) during the
summer following release. However, the average density of wild coho salmon
declined by 44% over the same period. Nickelson et al. 0 986) suggested that
the decline was due to the size advantage enjoyed by the larger hatchery coho
salmon in competitive encounters with smaller wild fish. Based on additional
studies (Chapman 1962; Mason and Chapman 1965; Chandler and Bjornn
1988), differences in fish size are known to be important in determining the
outcome of competitive interactions; larger salmonids
generally grow and survive better than smaller ones.

Studies by Miller (1954, 1958), Bjornn (1978), Petrosky and Bjornn (1988),
and Vincent 0 987) illustrate the complex and somewhat unpredictable
response of wild salmonids to supplementation. Miller (1954, 1958) found that
wild fish were able to outcompete stocked trout without incurring additional
mortality. Petrosky and Bjornn (1988) observed that the survival of wild
salmonids declined only at very high stocking densities. A compensatory
downward adjustment in the summer mortality rate of wild rainbow trout was
observed when 400 catchable-size rainbow were released into a 146-m section
of stream (Petrosky 1984). At low and intermediate stocking densities (50 and
150 fish, respectively, per 106-m sections), densities of wild rainbow trout in
Big Springs Creek were no different than in previous years of no stocking. This
implies that hatchery vs. wild trout competition was muted due either to (1)
significant losses (mortality or emigration) of hatchery trout, or (2) a non-
limiting supply of resources. The former explanation seems justified: only 1 %
of the hatchery trout remained in the study sections a year after their release.

Vincent (1975, 1987) contended that hatchery fish had a significant effect
on the survival of resident wild salmonids. A 49% decline in wild trout
numbers in a previously unstocked section of O'Dell Creek, Montana, coincided
with introductions of hatchery rainbow trout, and the abundance of age 2 and
older brown trout and rainbow trout in the Madison River increased after
stocking was terminated. In an Idaho stream, the number and percentage of
older resident (non-anadromous) rainbow trout declined during 10 consecutive
years of stocking of steelhead fry (Bjornn 1978). The steelhead fry competed
successfully with the age-0 wild rainbow trout and reduced the number of wild
fish that survived the first summer.

Salmon and Steelhead in the Marine Environment

In this section we discuss competitive interactions and the relative growth
and survival of hatchery and wild anadromous salmonids in marine
environments. Because few studies have addressed these topics within the
context of supplementation, much of the following synthesis is based on
results obtained from more general studies of marine salmonid ecology.

. The ocean segment of the anadromous salmonid life cycle consists of
several distinct migratory phases, including estuarine, coastal, offshore, high
seas, and return to freshwater. During this time fish gain approximately 98%

of their final body weight (Peterman 1987) while survival rates are typically less
than 15% (Foerster 1968; Bley and Moring 1988).

In general, hatchery fish experience higher mortality rates than wild
salmonids from the same river system (Bley and Moring 1988; Raymond 1988;
Piggins 1989). Rates of return for hatchery spring chinook salmon and
steelhead trout from the Snake River were lower, by as much as one order of
magnitude, than return rates estimated for wild stocks during 1966-1984
(Figure 3A and B). The record 1982 return for hatchery steelhead stands in
sharp contrast to the extremely low rates recorded for hatchery spring chinook
salmon. Raymond (198.8) believes that disease-related mortality may have
decimated hatchery chinook salmon smolts either en route or upon entry into
saltwater.

In Ireland, Piggins (1989) reported a 3.6:1 ratio of wild-to-hatchery Atlantic
salmon returns. Isaksson 0 979, cited by Bley and Moring 1988) obtained
similar results (2.8:1) for Atlantic salmon escapement to Icelandic streams.
Bley and Moring (1988) summarized references (included in Table 7) and
reported an average smolt-to-adult survival of wild steelhead trout of 13%,
compared to 5% for hatchery-produced fish. Marine survival rates have on
occasion been higher for hatchery-produced fish than for wild fish. In an
Oregon study (Aho et al. 1979), hatchery and wild steelhead trout were reared
to smolt stage in a hatchery, released, and enumerated upon their return as
adults. Return rates were,higher for progeny of hatchery fish in one year, and
for progeny of "wild" fish in a second year.

Competition between hatchery and wild salmonids in the ocean has not been
unequivocally demonstrated, because there is little or no competition, or
perhaps because of the complexity of factors involved (see Mathews 1984 for
a review), a paucity of experimental data, and natural variability in the
occurrence of competition and its effects. Nevertheless, noting'that(l)
hatchery-reared fish forage successfully upon reaching the ocean (Paszkowski
and Olla 1985a, 1985b), (2) food production is frequently patchy in time and
space (Healey and Groot 1987), (3) migratory salmonids remain in fairly
cohesive groups (Pearcy 1984), (4) migration routes of different stocks and
species may overlap, and (5) ocean distributions do not change significantly
either seasonally or with fish age (Healey 1986; Healey and Groot 1987), one
could conclude that competition is possible between hatchery and wild fish in
the ocean, particularly in nearshore areas and during periods of low
productivity.

Peterman, in a series of publications (1977, 1978, 1981, 1982, 1987,
1989), has championed the view that, for many salmonid species, survival and
growth rates in the ocean depend on stock abundance. Interpretations of the
data available have been conflicting. Analyses provided by McGie (1981,
1984), ODFW (1981), McCarl and Rettig (1983), Peterman and Routledge
(1983), and Emlen and Reisenbichler 0 988) favor the interpretation that marine
survival of Oregon coho salmon has been limited by density-dependent factors.
The opposite conclusion, drawn from the same data set but based on different
model specifications and data manipulations, was reached by Peterman 0 981),
ODFW 0 98 1), Clark and McCarl (11983), and Nickelson (1986), who provided a
synopsis of the debate. The failure of the escapement of adult coho salmon
from the Oregon Production Index Area to continue rising despite increased
releases of hatchery-produced smolts since about 1970 (Figure 4) added to the

Chinook Salmon

7.0

8.0
Wild fish

Hatchery fish
5.0

4.0

Adult Return
3.0

2.0

1.0

0.0

as 70 75 so 85

Steelhead Trout

7.0

6.0

5.0

4.0

Adult Return

3.0

2.0

1.0 B.

0.0

65 70 75 80 85

Year of Return

Figure 3. A comparison of the 1964-1984 rates of return of hatchery and wild
spring chinook salmon (A) and steelhead trout (B) from the Snake River
drainage. Data are from Raymond (1988).

SMOLrs

z
z
4

ADULI'S
Cr
UJ Ui to

2
V ItV"

0 L
1960 1965 1910 1975
YEAR OF SMOLT MIGRATION

Figure 4. Recent (1976-1985) trends in the number of hatchery smolts
released and the escapement of adult coho salmon from the Oregon Production
Index Area. Taken from Nickelson (1986).

debate about density-dependent survival in the ocean. The marine survival of
hatchery coho salmon released during years of strong coastal upwelling was
about twice that in weak upwelling years, but survival of both hatchery and
wild fish was lower during years when sea-surface temperatures were lower
than average (Nickelson 1986, Peterman 1989). McGie (1984) and Peterman
and Routledge (1983) reported a non-linear relationship between smolts
released and adult production for years of weak upwelling, implying density-
dependent mortality, at least during low productivity periods.
I
Additional evidence of density-dependent growth or survival in saltwater has
been presented by Anderson and Bailey (1974), Anderson and Wilen (1985),
Rogers (1980, 1984), McDonald and Hume (1984), Eggers et al. (1984), and
Reisenbichler 0 985). Of particular interest are data which suggest that
interspecific competition between adult chum and pink salmon in Puget Sound
may affect their mutual survival (Reisenbichler 1985).

Levy and Northcote (1981) concluded that the marine survival of chinook
salmon was determined to a large extent by the duration and quality of
estuarine residence. Length of estuarine residence is dependent on species,
developmental stage, food quantity and quality (Mason 1974), river discharge
and tidal influences, and estuarine topography (Iwamoto and Salo1977).
"'0'- rS

ADUIIS

Levings et al. (1986) reported that the presence of hatchery chinook salmon
did not affect residency times and growth rates of wild juveniles in a British
Columbia estuary and the adjacent foreshore region. Hatchery fish used the

estuary for about one-half the length of time that wild fry were present (40-50
d). Other investigators provide evidence that competition between hatchery
and wild salmonids could occur and cause growth and survival to be density-
dependent in estuaries (Reimers 1973; Bailey et al. 1975; Levy and Levings
1978; Healey 1979, 1982; Simenstad et al. 1979; Neilson et al. 1985).

Adults in Freshwater

Anadromous salmon and trout are renowned for their homing abilities and the
reliable timing of their spawning migrations. Reviews of these topics may be
found in Banks (1969), Leggett (11977), Brannon (11982), and Hasler and Scholz
(1983). Although recent research has advanced our understanding of how
salmonids are guided in their movements (McIssac and Quinn 1988), there
have been few comparative studies of the migratory abilities or inriver survival
of hatchery versus wild adults. The obvious question, "Does supplementation
adversely affect the spawning migration of wild salmonids?" cannot be
definitively answered from the information at hand.

Migratory tendencies and homing accuracy varies considerably between
species and strains of salmonids (Webster and Flick 1981; Kincaid and.Berry
1986). Straying of wild fish was the means of colonizing most drainages
covered by the last ice sheet and still represents a potential source of new
genetic material. Straying by hatchery fish, however, may be a detrimental
infusion of genes into a wild stock if large numbers of hatchery fish stray and if
their genetic makeup is significantly different from the wild stocks. There is
evidence that the progeny of transplanted pink (Bams 1976) and Atlantic
salmon (Stabell 1981, 1984) home less precisely than locally adapted stocks,
but such was not the case for coho salmon (Reisenbichler 1988).

The accuracy with which hatchery fish return to the hatchery or stream into
which they are stocked is influenced by stocking and transportation practices.
Straying rates increase if the release from the hatchery is delayed until after
smolt transformation is complete (Peck 1970; Larson and Ward 1954; Scholz et
al. 1978), if portions of the downstream migration route are bypassed (Hansen
et al. 1989), and as the distance between the hatchery or parental stream and
release site increases (Lister et al. 1981; Gunnerod et al. 1988). Hatchery fish
can return with high fidelity to the stream where they were planted, and to the
area of release (Wagner 1969).

A high incidence of straying is generally unacceptable from a
supplementation standpoint because of harvest complications and the
possibility that, if spawning occurs, wild stocks might be adversely affected
(Buchanan and Moring 1986; Evans and Smith 1986). Assuming that stocked
hatchery fish can be induced to home with some precision, managers may be
able to (1) reduce the sport harvest of wild stocks while increasing the catch of
hatchery-produced fish, (2) optimize the distribution of naturally spawning fish,
and (3) better seed the streams with naturally-produced fry.

Behavioral interactions between migrating hatchery and wild salmonids
appear to have little effect on supplementation programs. Overcrowding in
prime holding areas may increase the dispersal of adults (Cramer 1981),
possibly to the detriment of displaced fish.

We found little information to evaluate the claim that natural mortality rates
differ, between upstream hatchery and wild migrants. Leider et al. (1986)
argued that the lower abundance of repeat spawners among hatchery-produced
steelhead trout relative to wild fish was due to higher mortalities of hatchery
steelhead during repeat spawning migrations. The basis for this conclusion
was not determined, but the authors suggested that energetic bankruptcy
among hatchery fish following the initial migration may have contributed to
their poorer survival. Rosentreter (1977) also reported a low incidence of
repeat spawners for hatchery winter steelhead in an Oregon stream.

Surplus hatchery spawners have at times been returned to the river to
provide anglers with an additional opportunity to harvest them (Buchanan and
Moring 1987). Adults transported and released downstream from their natal
hatchery usually return rapidly and offer little opportunity to anglers (Bjornn
1986). Adults distributed upstream may also return to the site where they
were released as smolts, but the likelihood of doing so diminishes as the
transportation distance increases (Reingold 1975; Cramer 1981). The primary
drawback of returning surplus adults to the fishing areas is the possibility that
the fish will not be caught and may stray into spawning areas where they are
not wanted (Buchanan and Moring 1987).

The relative success of wild and hatchery fish spawning in natural
environments has been studied in recent years, and there is evidence that
hatchery adults may produce fewer smolts and returning adults than wild adults
(Leider et al. 1986; Chilcote et al. 1986; Nickelson et al. 1986). In studies of
steelhead in the Kalama River (Washington), Leider et al. 0 986) and Chilcote et
al. (1986) found low reproductive success among naturally spawning hatchery
fish compared to wild spawners. Although hatchery spawners outnumbered
wild spawners by at least 4.5 to 1, only 62% of the naturally produced
steelhead smolts were offspring of hatchery fish. Differences in viability were
thought to be a consequence of earlier than normal spawning by hatchery
steelhead.

Stocking of coho salmon presmolts into selected, Oregon coastal streams
boosted juvenile densities (at the expense of juvenile wild coho salmon), but
did not increase the number of returning spawners compared to unstocked
streams. The adults returning from presmolt releases spawned several weeks
earlier than wild fish, and Nickelson et al. (1986) concluded that the early
spawners, primarily hatchery fish, contributed little to natural production. The
density of the later spawning wild coho salmon returning to the stocked
streams was about half that observed in unstocked streams. After stocking
ceased, densities of naturally produced salmon fry averaged 32% less in the
formerly stocked streams than were found in the streams that had never been
stocked.

Whether hatchery and wild fish interbreed depends on their relative
abundance, the degree of spatial and temporal overlap, and the outcome of
sexual competition for mates and spawning sites. In the study of steelhead in
the Kalama River, the spatial and temporal overlap among hatcheryand wild
spawners was sufficient to permit crossbreeding (Leider et al. 1984).
Differences in primary (e.g., egg size and fecundity) and secondary (e.g., body
coloration and size) sexual characters between hatchery and wild spawners
may lead to unequal reproductive contributions by members of the respective
groups (Schroeder 1981; Gross 1985; Fleming and Gross 1989; Foote 1989).

Precfation

Predation is a major source of mortality for anadromous salmonids both in
freshwater and in the ocean - estimates range as high as 98% (Fresh et al.,
unpubl. manuscript).

Fish are believed to be the'major predators of hatchery and wild salmonids,
but predation by birds and mammals can be substantial (Elson 1962; Fraser
1974; Mace 1983; Ruggerone 1986; Wood 1987). Few direct estimates of the
severity of these losses are available. Based on dietary studies and relative
abundance estimates, the primary freshwater consumers of hatchery fish in the
Pacific northwest include salmonid, cyprinid, and cottid fishes, and mergansers,
kingfishers, and gulls. Blue sharks, sea lions, and harbor seals are encountered
in coastal regions, whereas sharks and lampreys are major predators in the high
seas (Ricker 1976).

Losses to predation may be higher for hatchery fish than for wild salmonids
because of inappropriate avoidance and foraging behaviors, an inability to
accurately assess predation risks, secondary stress effects, and a general
unfamiliarity with their new surroundings for the hatchery fish. Several studies
(MacCrimmon 1954; Piggins 1959; Kanidyev 1966; Larsson 1985) have
revealed intense post-release predation mortality among hatchery-reared
salmonids. Brown trout, for example, prey heavily on stocked Atlantic salmon
fry during the first few days after stocking (Mills 1964). Kanid'yev (1966)
reported that predators consumed 14-30% more hatchery-reared chum salmon
than wild chum fry during the first month following release. Studies by Bams
0 967) and Mead and Woodall 0 968) suggest that artificially-propagated
sockeye salmon fry are more prone than wild sockeye fry to predation.
Hatchery fish were found to be more vulnerable to kingfisher predation than
were wild salmonids (Male 1966).

Predation mortality may increase when physiological stress, either natural or
man-caused, is induced in hatchery-reared and wild fish (Congleton et al.
1985). Juvenile salmonids, while stressed, may have impaired swimming
ability (Schreck et al. 1985). Sources of stress include poor water quality,
disease pathogens and parasites, overcrowding, handling, transportation
(Specker and Schreck 1980), and situations requiring extraordinary physical
exertion (e.g., passage through dams and diversions; Fresh et al., unpub.
manuscript).

Environmental factors such as light intensity, discharge, turbidity and water
temperature play important roles in determining the magnitude of predation
mortality (Ginetz and Larkin 1976; Sylvester 1971). Variation in the amount of
predation by resident brown trout on planted Atlantic salmon fry was found to
depend on habitat type (MacCrimmon 1954). Tagmaz'yan (1971) noted that
predation was less severe in larger rivers than in small streams due to their
frequently turbid nature, fast current, and larger volume of water. Predation
rates during seaward migrations appear to be negatively correlated with stream
discharge (Hvidsten and Hansen 1988), presumably because transit times are
shortened and higher turbidities reduce the chance of detection by predators.

Salmonids released from hatcheries at sizes larger than wild residents are
potential predators, whereas fish stocked as smaller individuals are potential
prey. The apparent susceptibility of small fry to predation suggests that older

life stages may have greater survival potential (Mead and Woodall 1968;
Warner 1972). Cannibalism of hatchery-reared salmonid fry by wild resident
fish is common (Symons and Heland 1978; Kennedy and Strange 1986; Semko
1954a, 1954b). Conversely, hatchery salmonids may prey on wild fish or
cannibalize their own; as, for example, when yearling fish are released when
wild fry are emerging from redds (Reisenbichler 1986b; Nietzel and Fickeisen
1990). Sholes and Hallock (1979) reported that 0.5 million yearling chinook
salmon stocked in the Feather River, California, ate 7.5 million wild chinook and
steelhead fry. Levings and Lauzier (1988), however, found no evidence of
cannibalism of emigrating wild chinook fry by larger hatchery smolts in the
Nicola River, British Columbia. The authors suggested that wild fry avoided
predation by remaining in the shallow margins of the river.

The extent of predation upon non-salmonid species by hatchery salmonids is
not well-known (Evans and Smith 1986). Pisciverous hatchery-reared brown
trout, however, were observed to consume fish of other species roughly in
proportion to their abundance (Garman and Nielsen 1982). Millard and
McCrimmon 0 972) suggested that, in some cases, intra- and interspecific
predation may be buffered by the presence of stocked fish.

Even when they are not pisciverous, hatchery salmonids may expose wild
fish to greater predation risks. Competitively displaced wild fish may be more
conspicuous through their movements or residence in suboptimal habitats.
Large concentrations of hatchery fish may adversely affect wild juveniles by
stimulating numerical (e.g., at dams, river mouths, etc.) and functional
responses among bird and fish predators. In many cases predation mortality is
nonlinear and depensatory so that the proportion of fish eaten is greater when
prey populations are small (Figure 5A, 513) (Neave 1953; Hunter 1959;
Peterman and Gatto 1978; Mace 1983; Wood 1984). This type of predation
mortality was termed type-11 predation by Holling 1973. An alternate form of
predation, called type-III predation, may be compensatory at low prey
abundance, but depensatory at higher densities (Figure 5C). Since wild smolts
are frequently dwarfed in number by hatchery releases, we would expect
disproportionately higher mortality rates among the wild fish.

The vulnerability of hatchery and wild salmonids to predation depends on a
number of factors. During underwater observations of predatory attacks by
large rainbow trout on mixed groups of outmigrating hatchery and wild chinook
salmon in the Wenatchee River, Washington, Hillman and Mullan (1989)
reported that wild fish were preferentially preyed upon, probably because they
were half the size of the hatchery fish. In 23 attempts (all successful), the
trout caught and ate wild fry on all but one occasion, when a hatchery chinook
salmon was taken. In other studies, there was either no difference (Hvidsten
and Lund 1988) or higher levels (Osterdahl 1969; Ruggles 1980) of predation
on hatchery-produced smolts compared to wild smolts.

The effect of predation on hatchery and natural salmonid production has
been further revealed by predator removal experiments. Better survival of
stocked Atlantic salmon fry was obtained by reducing the population of
predators in several Scottish streams (Mills 1969). Survival of hatchery
steelhead fry stocked in an Idaho stream doubled following removal of fish
predators (Horner 1978). Sekulich (1980) found that 49% of the age 0 spring
chinook salmon introduced into another Idaho stream remained in pools from
which predaceous brook and steelhead trout had been removed, compared to

80-

60-

OL -
0 0
U 40-

01
0 200 480
No. Chinook Fry

6
E 0
Ln 4

0
0 \0\0
2

0
0 100 200 300
Smolt density (thousands)

100-
8
0-
0
2 60
C
40

20
d- 01
',e
o 0 0.6 1.2 1.8 2.4 3.0
Fry (millions)

Figure 5. Examples of predation mortality rates of juvenile salmon. Percentage
of chinook fry captured by (A) Bonaparte's gulls during 5-minute trials (after
Mace 1983), and (B) mergansers on a daily basis. (C) Percent daily predation
0

on pink salmon fry by coho salmon smolts and trout. Taken from Peterman
(1987).

only 15% in unmanipulated pools. The survival of Atlantic salmon to adult
stage. was three times higher when smolts were released in the ocean rather
than upstream in the river to bypass predation during downstream migration
(Hvidsten and Mokkelgjerd 1987).

Similar reductions in predation mortality have been reported when avian
predators were removed or reduced in abundance. Huntsman (1941) and Elson
0 962) were able to increase Atlantic salmon smolt production by 200-500%
by reducing the number of pisciverous birds (primarily mergansers). Avian
predators such as gulls and mergansers are opportunistic foragers (MacDonald
et al. 1988); if juvenile salmonids are abundant or otherwise conspicuous
relative to other species, they become the preferred prey (Wood 1987).
Further, bird predators congregate.in favorable feeding areas, such as near
hatchery release points ('Mace 1983). In the Columbia River, ring-billed gulls
flock to hydroelectric facilities during the spring to feed on migrating salmonids
that are killed, wounded, or disoriented as the pass through or over the dams
(Ruggerone 1986).

Dams on the Columbia River and other regulated streams of the Pacific
Northwest have created conditions'that are generally unfavorable for migrating
salmonids. The number and diversity of piscivorous fishes has increased in
mainstem reservoirs. Exotic species such as the walleye, smallmouth bass, and
channel catfish - all predators of juvenile salmonids - have become prominent in
reservoir fish communities (Maule and Horton 1984; Gray and Rondorf 1986).
At the same time, reservoir refill operations and the backwater effects of dams
have increased the length oftime that smolts are exposed to predators during
their seaward migrations.

The northern squawfish preys on both wild and hatchery juvenile salmonids
in lower sections of the Columbia and Snake Rivers (Thompson 1959; Sims et
al. 1977; Gray et al. 1983, 1984, 1986; Nigro et al. 1985; Palmer et al. 1986).
Squawfish concentrate in tailrace areas of dams where they are able to feed on
seaward migrants (Palmer et al. 1986; Faler et al. 1988). Sims et al. (1977)
found, salmonid remains in 21 % of squawf ish captured directly below Lower
Granite Dam on the Snake River. Squawfish predation on salmonids was
higher in fish collected near dams on the lower Columbia River than in those
collected away from dams (Gray et al. 1983). Near stocking locations and
during periods of hatchery releases, Thompson (11959) reported that juvenile
salmonids made up 87% of the fish consumed by northern squawfish in the
lower Columbia River. Buchanan et al. (1981), on the other hand, found
salmonid remains in only 2% of the squawfish collected in free-flowing sections
of the lower Willamette River.

As prey populations become more prolific, diverse, and stable in the
Columbia and Snake River reservoirs, the abundance of predators will no.longer
be constrained by short-term annual supplies of outmigrating wild smolts.
Shifts in predator type and abundance that come with altered species
associations, and perhaps with increased hatchery production, have led to
higher predation mortalities among wild juveniles during migration (Li et al.
1987). Theoretically, inflated predator populations can decimate wild stocks,
either trapping them at low levels of abundance or pushing them toward
extinction (Peterman and Gatto 1978; Ney and Orth 1986; Peterman 1987).

The effect of adding large numbers of hatchery fish to a basin, such as the
Columbia River, on predation in the estuary and marine environments has not
been studied to our knowledge. Mortality from predation is variable during the
estuarine phase. Several North American workers reported that predation on
salmonids in estuaries is low (Myers 1978; Simenstad et al. 1982; McCabe et
al. 1983; Myers and Horton 1982). But in recent studies by Norwegian
researchers, predation losses in estuaries ranged up to 25% of the smolt
population (Hvidsten and Mokkelgjerd 1987; Hvidsten and Lund 1988). No
significant difference was found in the predation rate (20%) on wild and
hatchery-reared Atlantic salmon smolts in the estuary of the River Orkla,
Norway. Piggins and Mills (1985), however, observed that hatchery-produced
smolts survived less well at sea than wild smolts by a factor of four which the
authors theorized was due in part to differences in predator avoidance
behavior.

The intensity and magnitude of predation in estuaries depends in part on the
duration of residence, the types and numbers of predators present, and the
bathymetric and hydrographic properties of the estuary. For some species, the
smaller the fish is upon reaching the estuary, the longer the duration of
estuarine residence (Simenstad et al. 1982). Levings et al. (1986) reported
that wild juvenile chinook fry remained in the Campbell River estuary for up to
twice as long (2 months) as larger hatchery chinook. The stay in the estuary of
some salmonid species may, in fact, lost for a much shorter period. Healey
(1979) estimated residence times of 0 - 18 d for chum fry in a small British
Columbia estuary. Hvidsten and Mokkelgjerd (1987) suggested that Atlantic
salmon smolts migrated through the River Surna ,(Norway) estuary in less than
a day. Other authors (Fried et al. 1978; McCleavb 1978) have reported
relatively rapid estuarine migrations, with the direction and rate of seaward
movement being strongly influenced by wind and tide-induced currents.

A negative correlation between abundance of pink salmon and the
production of coho salmon in hatcheries in Hood Canal, Washington, was put
forth as evidence of predation by the larger coho salmon on pink salmon fry
shortly after their release (Ames 1981). Gunsolus (1978) suggested that
predation of coho adults on coho smolts influences coho survival. Favorite and
Laevastu (1979) proposed that sockeye salmon smolts are less vulnerable to
predation when strong upwelling currents transport them offshore away from
predators. Increased predation mortality among salmonids may occur during
years when more preferred prey are scarce (Holtby 1988). Variations in
predation mortality rather than decreased food supply has been suggested as
the primary factor affecting Oregon coast coho salmon cohort strength (Fisher
and Pearcy 1988).

Fishing Mortality

The relative susceptibility to angling of wild versus hatchery juvenile fish,
and the effect of adding hatchery fish to a drainage on the harvest of wild fish
varies with the situation. In some circumstances, hatchery fish are more
vulnerable to angling than wild fish (Parker 1986; Marnell 1986; Boles 1960;
Flick and Webster 1962; Calhoun 1966; Cordone and Frantz 1968; McLaren
and Butler 1970; Rawstron 1972; Hunt 1979; Dwyer and Piper 1984). In
others, such as for brook trout in several Michigan lakes, fishing mortality was
greater for wild than for hatchery brook trout (Gowing 1978). Based on
underwater observations of the faster reaction times by wild steelhead trout

compared to hatchery rainbow trout when presented with lures, Hillman and
Chapman (1989) concluded that wild juvenile steelhead were more vulnerable
to angling.

Hatchery trout stocked in areas with wild trout could theoretically play a
variety of roles in influencing the harvest of the wild fish. Increased numbers
of anglers may be attracted to streams where large numbers of hatchery
steelhead smolts or catchable-size rainbow trout are released and overharvest
juvenile wild steelhead unless they are protected by regulations that prevent
their harvest. Pollard and Bjornn (1973) reported that the number of wild
steelhead trout caught from Crooked Fork, Idaho, was unaffected by the
presence of catchable-size hatchery trout; the wild trout were caught more
readily than the hatchery trout, and the hatchery trout did not buffer harvest of
the wild fish. Hazzard and Shetter (1938) reported that the catch of wild
rainbow trout increased following the stocking of legal-size hatchery trout,
presumably because of increased fishing effort. The harvest of larger
anadromous presmolts by angling could lead to- fewer adult returns due to
reduced smolt production and greater mortality among the remaining, small
smolts (Wagner 1968). Even if harvesting wild fish is prohibited, catch and
release fishing can have negative consequences, including delayed hooking
mortality (Wydoski 1977), increased susceptibility to natural mortality, and
disruptions of existing social hierarchies (Lewynsky and Bjornn 1987).

The effect of supplementation on angling related mortality for adult wild
salmonids can be severe if large numbers of hatchery fish are available for
harvest and the wild fish are not protected in some way. Catch-and-release is
commonly used to protect the wild fish, and can be quite effective, but even so
angling-induced stresses and mortalities can be significant (Wydoski et al.
1976; Bouck and Ball 1966; Stringer 1967). Stress caused by hooking did not
affect the homing accuracy of hatchery steelhead trout (Reingold 1975). Pettit
(1977) found no difference in the viability and development of eggs from
female steelhead that had been caught, released, and survived to enter the
hatchery versus fish that had not been caught.

When hatchery fish are produced to supplement a natural run, a common
management goal is to maximize harvest while maintaining a desired level of
natural production. Fishing pressure usually increases as the total availability of
fish increases, requiring careful regulation of exploitation rates and fishing
seasons to avoid over-harvesting the wild stock (Evans and Smith 1986).
Excessive harvest of the naturally-produced fish can be avoided either by
restricting the catch (Reisenbichler 1986a), by marking all hatchery fish and
requiring that unmarked wild fish be released (Reisenbichler 1986b), by
adjusting the timing and distribution of harvest through stock selection and
hatchery practices, by trapping and releasing hatchery adults into protected
areas, and by establishing terminal (i.e., spatially distinct) fisheries (Evans and
Smith 1986).

Disease

Disease must be considered within the framework of supplementation
because of its role as a mortality agent. The is copious amounts of information
on the incidence and effects of disease on salmonids within hatcheries. Our
understanding of the effects of disease on free-ranging hatchery and wild fish
is much more tenuous. Disease is thought to result in significant post-release

mortality among hatchery fish, being either directly responsible or predisposing
fish to mortality from other causes. We have found little evidence to suggest
that the transmission of disease from infected hatchery fish to wild salmonids is
widespread. However, there has not been much research on this subject and
since most disease-related losses probably go undetected (Goede 1986), we
conclude that the full impact of disease on supplemented stocks is probably
underestimated.

Fishery managers are generally aware of the potential for introducing
infectious microparasites (defined to include viruses, fungi, bacteria, and many
protozoans) and macroparasites (protozoans, helminths, and arthropods) into
natural or wild salmonid stocks through the production and release of fish from
hatcheries. Infectious diseases can theoretically be transmitted between two or
more stocks, hatchery-produced or wild, having susceptible fish which come in
contact with the pathogen. For example, hatchery stocks may be
contaminated by fish, eggs, or water transported from other facilities. Surface
water supplies used and discharged by hatcheries are rarely pathogen-free
(Wolf 1972; Frantsi et al. 1975), so that water-borne diseases are not easily
treated or contained. Hatcheries may act as reservoirs of infection due to
conditions or practices which increase the vulnerability of fish to infection and
maintain pathogen populations at infective levels (Goede 1986). Disease
problems may persist in hatcheries as a consequence of contaminated water
supplies and reproductive or vertical transmission of intracellular pathogens
such as viruses. The perpetuation of infectious hernatopoietic necrosis virus
OHNV) among many species of salmonids in Columbia River basin hatcheries is
an example (Mulcahy et al. 1983; Groberg and Fryer 1983).
Hatchery stocks which show no outward sign of disease or parasitism may
nevertheless contain fish carrying latent and infective doses of disease.
Avoiding detection, subclinically infected fish are probably released into natural
waters more often than is realized (Marnell 1986). Even under favorable
conditions, latent infections may limit the success of hatchery fish released into
natural habitats. At worst, virulent pathogens may be introduced into areas
where they previously did not exist, causing catastrophic losses and the
decimation of entire stocks of fish. Exposure to pathogens may potentially
affect both hatchery and wild salmonids by (1) increasing levels of mortality,
(2) increasing sensitivity to stressors, (3) impairing performance, and (4)
modifying the genetic composition of the infected population. We direct the
reader to Goede 0 986) for an excellent summary of these problems.

Disease outbreaks are a relatively common occurrence in hatcheries, often
requiring therapeutic treatment and sometimes the wholesale destruction of
diseased fish. These efforts do not always meet with success. Recent results
point to the failure of control methods to eliminate epizootics of bacterial
kidney disease (BKD) among hatchery stocks of Columbia River spring chinook
salmon (Elliott et al. 1989). Average rates of return of hatchery-produced
spring chinook salmon adults were negatively correlated (r = -0.72; calculated
from data presented in Table 2 of Raymond (1988)) with the number of
hatchery smolts migrating past the uppermost dam on the Snake River during
1966-1984. During the same period, wild chinook salmon returned at an 80%
higher rate than did hatchery fish (2.3% vs. 1.3% average rate of return).
Even during years of improved in-river survival of hatchery smolts, the return of
adults was lower than expected. From this, Raymond (1988) concluded that
problems other than mortalities at dams were affecting hatchery stocks of

spring chinook salmon. Most researchers (e.g., Raymond 1988; Williams
1989) now believe that low stress tolerance coupled with a high incidence of
BKD in yearling chinook salmon smolts is the major factor limiting spring
chinook salmon production at Snake River basin hatcheries. Experimental
evidence suggests that BKD interferes with the ability of salmonid smolts to
acclimate to seawater, and that exposure to seawater actually accelerates
mortality among infected fish (Fryer and Sanders 1981; Banner et al. 1983;
Banner et al. 1986; Congleton et al. 1985). Banner et al. (1983, 1986) and
Congleton et al. (1985) present data indicating that BKD-infected spring
chinook smolts from several Oregon and Idaho hatcheries suffered heavy
mortalities (up to 85%) after being held for several months in seawater. Many
questions remain regarding the relationships between the. incidence of disease
in wild and hatchery stocks, physiological changes associated with smolt
transformation, and survival in early ocean life.

Smoltification, the handling and confinement of fish during transportation,
delays in downstream fish passage at dams, entry into saltwater and numerous
other factors (e.g., temperature, pollution, etc.) all represent potential causes of
stress in salmonids (Sanders et al. 1978; Wederneyer et al. 1980; Specker and
Schreck 1980; Fryer and Sanders 1981; Banner et al. 1983; Congleton et al.
1985; Li et al. 1987). The role of stress in reducing the ability of the salmonid
immune system to respond to pathogens and other environmental stressors is
well documented (Wedemeyer 1970; Wederneyer and Wood 1974; Schreck
1981; Murphy and Kelso 1986). For example, stress-induced increases in
plasma cortisol are known to lower the natural resistance of fish to disease
pathogens (Pickering and Duston 1983; Angelidis et al. 1987). Aeromonas
hydrophila epizootics are precipitated by stress conditions (Bullock et al. 1971);
infections in salmonids are usually associated with stressful (i.e., elevated)
water temperatures (Groberg et al. 1978).

Survival, growth, swimming ability, and other performance measures are
compromised by the presence of disease, particularly in marginal habitats, after
hatchery fish are released (Goede 1986). Smith and Margolis (1970) and
Boyce (1979) found that juvenile sockeye salmon infested with tapeworm
(Eubothrium salvelinil were more prone to exhaustion, lower growth rates, and
higher mortalities than were unparasitized juveniles. Repeated measurements
on two groups of brook trout, one carrying the IPN virus and the other not, 2.5
y after their release into a lake indicated that the carrier fish were smaller by 5
to 8% (Yamamoto 1975). However, size differences were not apparent 6
years after stocking (Yamamoto and Kilistoff 1979).

The generally poor ecological performance of hatchery fish following
stocking (discussed in a previous section) may increase their vulnerability to
diseases prevalent outside of the hatchery. Hatchery fish are presumably
stressed by agonistic encounters with wild fish but to our knowledge no one
has addressed the effects of such stress in epidemiological terms. Social
interactions and status have a significant bearing on the severity of the stress
response in salmonids (Li and Brocksen 1977; Ejike and Schreck 1980).
Socially inferior hatchery fish may be more susceptible to infection following
release. A similar argument can be made for situations in which wild trout are
dominated by introduced hatchery fish. Petrosky and Bjornn (1988), however,
saw no evidence of extended periods of stress in resident rainbow trout
following the introduction of large numbers of hatchery trout.

In spite of the comparatively high incidence of disease among some
hatchery fish stocks, there is little evidence to suggest that diseases or
parasites are routinely transmitted from hatchery to wild fish. Work by
Yamamoto and Kilistoff 0 979) indicates that the IPN virus is not readily
transmitted to noninfected brook trout in natural systems. Spread of BKD from
heavily infected (100%) Atlantic salmon in the hatchery to wild fish was very
limited (< 1 % infected; Pippy 1969). From experimental stocking of hatchery-
reared brook trout infected with BKD and furunculosis, Allison (1961) and
McDermott and Berst (1968), respectively, concluded that there was little or no
communication of pathogens to resident wild brook trout. Mitchum et al.
(1979) suggested that wild (feral) brook trout were infected with BKD by
hatchery stocks, but did not provide conclusive evidence; hatchery trout last
stocked in 1963 were inferred to have been the source of an epizootic among
wild fish in 1976. Horizontal transmission of BKD from infected wild brook
trout to stocked salmonids in natural waters has also been reported (Mitchum
and Sherman 1981). Little is known of the prevalence of vertically transmitted
diseases among progeny of naturally spawning hatchery or hatchery x wild
salmonids.

The outcome of exposing wild stocks to infected hatchery stock - whether it
is fatal, debilitating, or benign - depends on ecological parameters which
influence the spread and pathology of the disease. If the incidence of wild
salmonids being infected by hatchery fish is low, it may be due to a reduced
probability of contact between individuals outside the confines of the hatchery,
a greater natural resistance to pathogens among wild salmonids, and
environmental conditions which are inimical to the survival and transmission of
the pathogen. Marnell (1986) suggests that the constraining influence of high
intermediate host-specificity among many fish parasites may limit their
distribution and abundance.

Natural immunity to diseases and parasites appears to vary among species
and stocks of salmonids (Sanders et al. 1970; Heggberget and Johnsen 1982;
Babey and Berry 1989; LaPatra et al. 1990). For example, it has been
postulated that members of the genus Onchorynchus may be more susceptible
to BKD than are species of the former Salmo genus (Evelyn et al. 1988).
Epizootics of the IHN virus occur in sockeye salmon, chinook salmon, and
steelhead trout, but coho salmon are immune (Li et al. 1987). Winter et al.
(1980) reported differences in BKD resistance among stocks of steelhead trout
and coho salmon. They also found that individual stocks may be resistant to
one disease (BKD) but highly susceptible to another (vibriosis). Variable
susceptibility to infection by the protozoan Ceratomyxa shasta, and
corresponding pre-spawning adult mortality, has been demonstrated for coho
salmon (Sanders et al. 1972; Hemmingsen et al. 1986), chinook salmon (Zinn
et al. 1977; Ratliff 1981) and summer-run steelhead (Buchanan et al. 1983).
Infection frequencies in stocks of these species from the lower Columbia River
and its tributaries appear to be much lower than in stocks from streams in
which the protozoan is absent (Hemmingsen et al. 1986). Johnels (1984; cited
by Stahl 1987) suggested that the introduction of hatchery-propagated Atlantic
salmon from Sweden (Baltic Sea stocks) was responsible for the rapid spread of
the skin parasite, Gyrodactylus salaris, in stocks of less resistant salmon in
Norway (Eastern Atlantic stocks).

Evidence is accumulating that resistance to pathogens among salmonids is
an inherited trait resulting from selection pressures. Immunity to several

diseases has been demonstrated to have a heritable basis in fish (Gjedrem
1983), although specific host cellular genes which confer a regulatory effect on
the outcome of disease in fish have yet to be discovered. McIntyre and Amend
(1978) demonstrated strong heritability for resistance to IHN in sockeye
salmon. BKD resistance in coho salmon differs among transferring genotypes
(Suzurnoto et al. 1977; Winter et al. 1980).

As is true of other vertebrate species (O'Brien and Evermann 1989),
salmonids have developed an elaborate array of immunogenetic defenses
against pathogens with which they have co-evolved, but may be hypersensitive
to exotic pathogens communicated by conspecifics and other closely related
hosts (Barbehenn 1969; Marnell 1986). Widespread use of chemotherapy to
control disease in hatcheries may result in the development of new, drug-
resistant strains of viral and bacterial pathogens by natural selection. The
consequences of exposing Wild stocks to novel pathogens that are both virulent
and readily transmitted may extend well beyond the economic impacts of the
disease. Epizootics, if severe enough, can affect both the genetic structure and
persistence of a species. Besides selecting for genotypes that confer immunity
on surviving fish, disease outbreaks can alter the frequencies of alleles at loci
affecting disease resistance (Allendorf et al. 1987), particularly when a large
contraction in population size occurs. An inverse correlation between
susceptibility to disease and genetic variability (allelic diversity) is suspected
because immune system response appears to be coded by genes that are
highly polymorphic (R. Waples, NMFS, pers. comm.). Significant losses of
allelic diversity at loci associated with disease resistance are likely to increase a
stock's susceptibility to epizootics.

Marnell (1986) has identified several conditions which, if met, increase the
probability of damage to natural immune systems: (1) fish have no
evolutionary association with a harmful pathogen present in the receiving
water, (2) hybridization occurs between hatchery fish and the wild stock, and
(3) long periods of time elapse between epizootics. The primary implication of
using hatchery and wild stocks which have different genetically determined
immune systems is that their progeny may be less resistant to endemic
diseases. Hemmingsen et al. (1986) demonstrated that the susceptibility to
infection by C. shasta by progeny of crossbred coho salmon was almost always
intermediate between the susceptibilities of fish from the parental stocks.

The specificity of fish immunogenetic defense systems may dictate that only
native or closely related stocks of salmonids be used for propagation.
Regardless of the source of broodstock used, stocking programs should include
monitoring and prophylactic treatment as needed to prevent the spread of
potentially harmful diseases (Griffiths 1983; Murphy and Kelso 1986). Fish
that are diagnosed as having a disease, or are even suspected of carrying a
disease, should not be stocked into waters where that disease has never been
detected (Evans and Smith 1986).

Supplementation Methodology

In this section we discuss various stocking variables that, through their
effect on the interaction and survival of hatchery and wild fish, can strongly
influence the success of supplementation programs. Supplementation

techniques that offer relatively easy and cost-effective means of regulating
contact between hatchery and wild fish include, but are not limited to, stocking
rates, size or age at release, and time and location of release. Successful
supplementation requires knowledge of stock-specific life histories and habitat
requirements; if the goal is minimize impacts to wild stocks, then hatchery fish
should be produced that are qualitatively similar to those stocks.

Rearing and Stocking Procedures

The quality of fish released from hatcheries influences their subsequent
survival and contribution as adults to the fishery and the spawning population
(Burrows 1969). Insight into the effects of hatchery rearing and stocking
procedures on the post-release survival of hatchery fish has been reported in
several studies, but we were unable to locate quantitative information which
describes the effects of various rearing and stocking procedures on wild or
supplemented stocks. Our discussion, therefore, focuses primarily on the
performance of hatchery fish.

Several abiotic and biotic factors affect the quality and production of
salmonids in hatcheries (Table 8). Environmental conditions can be controlled
within limits determined by site-specific factors (e.g., chemistry of water
source, and physical facilities) and hatchery operations. Rearing and feeding
(nutrition, frequency of feeding) techniques have improved to the point where
hatcheries are able to produce better quality fish, minimize disease problems,
and increase survival, without unduly sacrificing the quantity of fish produced.
Nevertheless, much work remains to be done to define and develop optimum
rearing strategies that conserve genetic resources and allow fish to survive,
grow, and reproduce following their release into streams (Reisenbichier 1986a).

Table 8. Environmental factors known to affect the quality and production of
salmonids in hatcheries (Parker 1986).

Physical Chemical Biological

Temperature Dissolved Gases Species
Pressure pH Genetics
Photoperiod Nitrogenous wastes Sex
Water Velocity Inorganic Ions Age
Cover Hardness Health
Substrate Alkalinity Physiological status
Salinity
Contaminants

Methods of stocking may affect the post-release survival of hatchery fish.
In some cases the stocking is relatively easy on the fish, as when fish are
released at the hatchery and allowed to leave the hatchery voluntarily. When
fish are stocked away from the hatchery, the juveniles are captured at a
hatchery, loaded into tank trucks, transported, and released into a lake or
stream (Barton et al. 1980). Several components of the latter process may
affect the subsequent performance and survival of hatchery-reared fish. Of

special concern is the amount and duration of stress which fish are subjected
to by, handling, confinement, transportation and release procedures. From the
by Specker and Schreck (1980) and Barton et al. (1980) we believe that
properly conducted stocking operations do not represent severe stressors to
fish.

Environmental stressors, while not necessarily lethal in themselves, may
disturb endocrine, metabolic, and osmoregulatory homeostasis (see Mazeaud et
al. (1977) for a review), leading to reduced fitness and subsequent mortality.
Handling and crowding can elicit a strong stress response in salmonids
(Wedemeyer 1972; Schreck et al. 1977; Strange et al. 1978), and may be the
most stressful aspects of the stocking operation (Specker and Schreck 1980;
Barton et al. 1980; Barton and Peter 1982; Congleton et al. 1984). In a study
of delayed mortality of stocked rainbow trout in Oregon, Horton (11956)
observed a pattern of gradually increasing mortality until the third or fourth
day, followed by a decrease and cessation by the end of a week's time.
Average delayed mortality in Oregon stocking operations ranged as high as
10% of the fish transported.

Tagging operations are probably significant causes of stress (Yamada et al.
1979) and mortality. Berg (1977) reported that the additional step of weighing
Atlantic salmon smolts at time of tagging reduced returns from 14% to 2.2%.
Tagged fish, if their appearance or swimming abilities are altered by external
marks, may not be able to interact normally in social and predatory situations.

The type of transport employed may influence stocking success. Air-
dropped brook trout yearlings experienced lower survival than trout released at
ground level in Ontario lakes (Fraser 1968). Congleton et al. (1984) reported
that chinook salmon smolts transported by barge from collection facilities on
the Snake River to the Columbia River estuary had significantly lower plasma
cortisol concentrations than did smolts transported by truck.

Variations in loading density apparently have little effect on stress levels or
mortality among transported salmonids, provided that water quality is not
compromised. Congleton et al. (1984) found no difference in plasma cortisol
concentrations in chinook salmon smolts held for up to 24 hours at three
loading densities (0.12, 0.25, and 0.50 pound/gal in transportation collection
facilities. Survival rates did not differ among test groups of coho salmon
smolts confined at low (12 g/L) and high (120 g/L) densities following
transportation (Specker and Schreck 1980).

Primary and secondary stress responses in salmonids associated with
outplanting operations can be ameliorated by ensuring good water quality
during shipment and avoiding excessive handling, crowding, and transit times.
High dissolved oxygen levels, reduced water temperatures, and salt
concentrations which help maintain osmotic balance are recommended for
transport and recovery water (McCraren and Millard 1978; Nikinmaa et al.
1983; Parker 1986).

Because hatchery salmonids require prolonged periods, up to a week in
some cases, to recover from a stressful situation (Strange et al. 1978; Barton
et al. 1980), it may be necessary to provide a recovery area following
transportation, particularly, if conditions in the receiving water would not allow
the fish to recover (Parker 1986). In a study designed to evaluate the effects

of post-stocking acclimation on hatchery-reared brown trout released into three
Welsh rivers, Cresswell and Williams (1982) observed less dispersal and higher
percentages of recapture among acclimated fish, but only under low flow
conditions. Miller (1954) found that hatchery-reared rainbow trout conditioned
in a stream survived better than unconditioned, pond-reared fish. Shustov et
al. (198 1) attributed poor dispersal by hatchery Atlantic salmon released into
the Kuzreka River (Kola peninsula, USSR) to poor physical conditioning and a
lack of endurance.

Stocking Densities and Rates

Optimal stocking densities and rates depend on (1) the objectives of the
project (e.g., enhancement vs restoration), (2) the distribution and carrying
capacity of the habitats into which hatchery fish are to be introduced, (3) the
proportion of limiting resources already used by resident fish, and (4) the
viability (survival and reproductive success) of hatchery- produced fish.
Determining the proper stocking rates for supplementation is more complicated
than that for stock establishment or restoration in that consideration must be
given to the abundance of wild fish relative to the carrying capacity of the
stream.

Optimal stocking densities for steelhead fry and Atlantic salmon have been
estimated by Hume and Parkinson (1987) and Cote and Pomerleau (11985; cited
by Bley and Moring 1988). Symons and Heland (1978) refined stocking
densities for hatchery-reared Atlantic salmon on the basis of age-specific
habitat requirements. Because space, food, and cover requirements vary with
fish size (e.g., Everest and Chapman 1972), the productivity and availability of
size-specific habitats must be considered when supplementing species which
spend more than one year in freshwater. Carrying capacities are higher and
-hatchery fish are more likely to learn to feed successfully in productive streams
than in infertile streams (Bjornn 1986). Aquatic productivity is determined by a
host of environmental factors, some of the more important being stream
morphology, flow regime, water temperature, dissolved oxygen, acidity,
allochthonous input, and the composition of the resident biota. In order to fully
utilize the productive potential of the stream and to reduce energetic costs and
predation losses, supplementation is probably best accomplished by releasing
fish in small groups in several locations (Cote and Pomerleau 1985 - cited by
Bley and Moring 1988; Hume and Parkinson 1987; Richards and Cernera
1989).

Hatchery managers should gauge the potential effects of releasing large
numbers of presmolts or smolts on predator populations. Relatively high
threshold densities of smolts may need to be released in order to significantly
reduce the risk of predation (Peterman 1977; Ruggerone and Rogers 1984;
McIntyre et al. 1989). Sufficient production of hatchery and wild fish
combined with prudent harvest management is required to avoid depensatory
losses to predators (including man), and to prevent the potential collapse and
equilibration of wild stocks at relatively low population levels (Peterman 1987).

Age and Size at Release

Most anadromous hatchery fish, including those reared for supplementation
purposes, are released as smolts with the expectation that they will migrate
seaward soon after release (Bjornn 1986; Lichatowich and McIntyre 1987).

Alternate strategies include stocking underutilized habitats with eggs, fry, or
parr (presmolts) and surplus adult fish. Each management approach is species
and situation specific and involves economic and biological tradeoffs.
Production costs are inversely related to the length of time that fish are reared
at the hatchery, but fish grown to a larger size generally return at higher rates
(Potter and Barton 1986). Production of wild salmonid smolts is less affected
by raising hatchery fish to smolt size before outplanting (Wagner 1967). There
are, however, genetic and disease burdens associated with prolonged hatchery
residencies (see earlier sections).

Stocking strategies other than smolt stocking require that the hatchery
juveniles rear in freshwater for a period before emigrating to the ocean (Bjornn
1986). Supplementation of natural stocks with presmolt life stages has
become a valuable management tool because: (1) it allows for greater
flexibility, efficiency, and volume in hatchery production, (2) more fish can be
produced from natural rearing areas, and (3) the potential for detrimental
genetic alteration is reduced. From a consideration of expected survival rates
and production costs, Hume and Parkinson (1988) advised releasing smaller
presmolts (fry) when the area to be stocked is small and a large number of
eggs are available. Stocking larger fish may be the best supplementation
technique when brood stock is scarce and a large amount of habitat is
available. If the population size of wild fish is dangerously low (i.e., small
relative to its potential), a conservative strategy might be to release smaller fish
into underseeded habitats at densities which are unlikely to result in the
displacement of the wild fish.

Several experiments have been reported or are currently underway to
evaluate the effects of age and size at release on supplementation. Seidel et
al. 0 988) noted that poststocking survival-to-adult of fall chinook fingerlings
raised in Washington hatcheries jumped from approximately 0.2% to 1.2%
when mean size at release was increased from 4 to 6 g. Reimers 0 979)
reported that survival to return of yearling chinook salmon released from the Elk
River hatchery (2.2%), although lower than that of wild salmon (4.3%), was
substantially higher than survival of fish released as underyearlings (0.3%).
Survival of fall-run chinook salmon from hatcheries on the Sacramento River
also appears to be positively related to release size (Reisenbichler et al. 1982).
Seelbach (1987) found that large yearling steelhead trout stocked in a Lake
Michigan tributary in the fall survived to smolt stage at a much higher rate than
did smaller fall-planted fingerlings and similar size, spring-planted yearlings. It
is not clear whether the results apply to other hatchery programs since the
experimental fish used in this study were first-generation offspring of wild
steelhead.

It is difficult to differentiate the effects of size of release from time of
release. Work by Bilton et al. (1982, 1984) indicated that release size and time
jointly affect the survival and average size of salmon returning to coastal
hatcheries. From an evaluation of survival rates for three graded size groups of
juvenile coho salmon released simultaneously on four separate occasions during
the spring and summer, Bilton et al. (1982) concluded that adult returns would
be maximal for late June releases of large juveniles. For the range of release
sizes and dates typically available to hatchery managers, time of release
apparently has a greater effect on survival than does size (Bilton et al. 1982,
1984; Mathews and Ishida 1989).

Size at release may also affect the size of adults returning to the hatchery
and, presumably, to spawn naturally; larger, faster growing smolts tend to
return at an earlier age and are smaller in size (Hager and Noble 1976; Bilton et
al 1982; Bilton 1984). Supplementation efforts may fail to produce the desired
results if early-maturing hatchery fish are unable to compete effectively for wild
mates or spawning sites.

Green (newly fertilized) or eyed eggs of hatc hery-s pawned anadromous
salmonids are frequently stocked in streams and artificial incubation channels
with the goal of augmenting natural production (Thomas 1975; Egglishaw and
Shackley 1980; Kennedy and Strange 1980, 1981). Survival to the fry stage
was lower for Atlantic salmon green eggs (1.4%) than for eyed eggs (10.3%)
stocked in a Scottish stream (Kennedy and Strange 1981). Egg-to-fry survival
varied inversely with stream gradient and resident fish densities (Kennedy and
Strange 1980, 1984). Overwinter survival rates of embryos and yolk-sac
larvae of wild and hatchery brook trout have been found to be similar (Flick and
Webster 1964).

Egg planting reduces the exposure of fish to artificial selection in the
hatchery but does not guarantee favorable results. Atlantic salmon from a
Scottish hatchery that were stocked as eggs in two streams in northern Spain
contributed significantly less to the adult in-river fishery than did native salmon.
The lower performance of the non-native eggs was thought to have resulted
from a combination of poor genetic adaptat.ion and inadequate stocking
methods (Garcia de Leaniz et al. 1989). Planting technique has been shown to
affect the survival of salmonid eggs and embryos; direct plants of eyed eggs of
brown trout produced more sac and swim-up fry than did Whitlock Vibert box
plants (Harshbarger and Porter 1982).

Although substantial mortality of outplanted eggs can be expected even
under the best conditions, optimal results are obtained when fertilization and
stocking mimic natural spawning times. Foerster (1938) and Bjornn (1978)
found no difference in the efficiency of supplementation of sockeye salmon and
steelhead trout, respectively, using egg planting and releasing button-up fry.

A variation of the egg outplanting technique is the stocking of strearnside
incubation boxes with fertilized eggs of hatchery or wild stock origin. If a
reliable supply of eggs from wild spawners can be obtained, egg boxes offer an
attractive means of supplementing natural production, with less dependence on
hatche ry-propa gated stocks of fish. Egg boxes require fewer resources, and
are simpler and more portable than more conventional methods of artificial
propagation, but do require reasonably good water quality.

Stocks can be supplemented successfully with age-O salmonids, particularly
in productive, underseeded habitats (Bjornn 1978). Fry fed for a short period
before release may survive better than unfed fry (Stewart 1963), if the fry
normally kept in the hatchery readily feed on the hatchery diet and do well.
Slaney et al. (1980) reported substantial yields from stocking steelhead trout
fry (mean weight 0.3 g) above migration barriers in a high-gradient stream.
Results from other studies, however, indicate that stocking hatchery fish at the
fry stage yields low survival rates and, consequently, low percentages of adult
returns (Wagner and Stauffer 1978; Seelbach 1987; Hume and Parkinson
1988). Hume and Parkinson (1988) found that larger and presumably less
vulnerable age-O steelhead released late in the growing season almost always

survived better than did smaller fish released earlier. The relative importance of
size and time-at-release could not be distinguished because they were highly
correlated.

The average size of fry released from the hatchery relative to that of
resident wild fry may affect the subsequent survival of both groups of fish. If
hatchery fish are stocked or emerge earlier than wild fish, they may enjoy a
competitive advantage (Fenderson et al. 1968) and reduce the survival of wild
fish emerging at the normal time (Solazzi et al. 1983; Nickelson et al. 1986;
Chandler and Bjornn 1988). Size-related effects can be avoided by imposing
spawning, incubation, and feeding schedules that ensure that the hatchery fish
are not present in the stream ahead of the wild fish and they are not larger than
the wild fish (Reisenbichler 1986a).

Size at release has also been found to correlate with poststocking survival
of older presmolts and smolts for steelhead (Larson and Ward 1954; Wagner
1968; Bjornn 1986; Seelbach 1987) Atlantic salmon (Meister 1969; Chadwick
1987) coho salmon (Hager and Noble 1976; Mahnken et al. 1982; Bilton et al.
1982) and chinook salmon (Hosmer et al. 1979; Seidel et al. 1988). Holtby
0 988), however, reported that larger wild coho salmon smolts survived no
better than smaller smolts from the same stock. Body size and smolt
transformation status may influence the rate and path of migration taken by
spring chinook salmon smolts released into the lower Columbia River (W.
Zaugg, NMFS, pers. comm.). Larger fish tended to migrate in mid-river,
whereas smaller fish remained close to shore. Migration rates were positively
correlated with size at release.

Body size has an effect on the percentage of fish of a given age that
become smolts and perhaps on the timing of seaward migration, particularly for
species that normally spend more than one year in freshwater. Even in the
presence of conducive exogenous stimuli (e.g., photoperiod), steelhead and
Atlantic salmon are likely to remain in freshwater for additional periods of time
if threshold sizes for smolting have not been attained (Bjornn 1986). For many
species, hatchery programs have been successfully implemented to shorten the
time required to reach smolt stage. Freshwater rearing periods for steelhead
and Atlantic salmon, normally lasting two or more years, have been reduced to
one year by providing increased temperatures and thereby growth rates in
some hatcheries. Similar efforts to produce viable age-0, rather than yearling,
coho and chinook salmon smolts have been less effective (Bilton and Jenkinson
1980; Bjornn 1986). Bilton et al. (1982) reported that "accelerated" age-O
coho salmon smolts returned at 'one-tenth the rate of age-1 (the normal
smolting age) smolts that had been released on the same day. Bjornn (11986)
observed that chinook salmon which normally became smolt as yearlings in the
spring, became smolts and migrated downstream in the spring about 9 months
after spawning if growth and development were accelerated in a hatchery, but
returned at lesser rates than yearling smolts from the same population. In both
cases, age-O fish were smaller than the corresponding age-1 smolts; probably
too small to survive in the ocean (13jornn 1986).

Time and Location of Release

Time and location of release are important in supplementation of wild stocks
because those two factors can help regulate the extent and magnitude of
interactions between hatchery and wild fish. Smolt releases from anadromous

fish hatcheries are usually timed to coincide with the outmigration of wild
conspecifics (Reimers 1979; Levings and Lauzier 1988). This practice yields
conflicting results: it helps to preserve genetic integrity and ensures higher
survival by mimicking natural outmigration, but it also increases the risk of
density-related mortality and undesirable interactions between hatchery and
wild fish. The objective and the result in most cases is the rapid movement of
hatchery smolts to the ocean, where density-dependent effects are presumed
to be less likely or less intense (Reisenbichler 1986a).

Chinook salmon and steelhead smolt releases from hatcheries in the Snake
River drainage are also scheduled to coincide with flow (i.e., "Water Budget")
releases and barge transportation schedules. Releases are timed to avoid
overlap between the two species because the smaller chinook may be stressed
by steelhead during transportation. Releases from Oregon hatcheries are based
on time with size criteria; release times are hatchery and species specific
(Nietzel and Fickeisen 1990).

Although smolt transformation is under the control of the seasonal
photoperiod cycle (Clarke et al. 1981), considerable variability in the timing of
the seaward migration of wild smolts occurs with fluctuation in temperature,
flow, and other proximate factors in the environment (Grau 1981; Solomon
1981; Holtby et al. 1989). Rapid migration and a decreased risk of competition
and predation may be facilitated by nighttime releases of larger fish under
conditions of high turbidity and flow (Ginetz and Larkin 1976). Unfortunately,
there are few data on ecological interactions between hatchery and wild
smolts, so the impact of supplementation at this life stage remains poorly
understood.

Time of release may affect the distribution of the fish in the marine
environment (Irvine and Ward 1989) and the timing of adult returns (Evans and
Smith 1986). For example, delayed smolt releases have been used to obtain
"non-migrating" stocks of salmon in the Puget Sound (Mahnken and Joyner
1973). Delayed releases may have the benefit of hastening downstream
migrations of hatchery smolts (Zaugg 1981, 1982; Zaugg et al. 1986), but also
risk causing increased residualism, lower survival, and increased straying of
returning adults if delayed for too long (Scholz et al. 1978). Fish released into
the Columbia and Snake Rivers from upriver hatcheries after the spring runoff
may have difficulty migrating through the reservoirs and be subjected to
increased turbine-related mortality (Seidel et al. 1988).

A portion of the hatchery fish released may either fail to emigrate or exhibit
a protracted downstream migration lasting for weeks or months (Levings and
Lauzier 1988). The survival of hatchery nresiduals" is generally thought to be
low (Seelbach 1987), although Reimers and Concannon 0 977) recorded higher
survival among chinook salmon that remained in the river for several months
following a June release from an Oregon hatchery. Mitans (1970)
recommended early spring stocking of smolt-age Atlantic salmon to allow non-
migrants more rearing time in freshwater. Studies by Wagner (1968), however,
suggest that early releases may be inappropriate; adult returns from smolt-size
steelhead trout yearlings stocked in February and March were much lower than
returns from releases in late April (the natural time of emigration). Hemmingsen
et al. (1986) demonstrated a similar reduction in survival when the release date
of coho salmon was advanced from July to May. Early releases of coho

salmon can increase predation on natural ly-prod uced pink and chum fry
(Johnson 1974).

Choices concerning the streams, stream reaches, and sites within a reach to
be stocked depend on management goals, accessibility, and the characteristics
of the receiving water. Release locations may be chosen with the aim of
minimizing losses of hatchery fish to predation (Thompson and Tufts 1964), to
dam-related mortality (Ebel 1970), and to lessening competition between
hatchery and wild fish (Nietzel'and Fickeisen 1990). Because anadromous
salmonids generally home to the stream, and often to the release area, from
which they emigrated as smolts (Wagner 1969; Hasler 1971; Power and
McCleave 1980), release locations can be chosen to facilitate the segregation
,or mixing of hatchery and wild stocks, depending on program goals. Careful
selection of release sites can help protect non-targeted wild stocks by
minimizing interactions, by diverting fishing pressure away from vulnerable
stocks, and by enhancing the opportunity to catch hatchery fish (Cramer
1981). Stocking programs set up solely to produce fish for harvest can lessen
effects on wild fish by concentrating releases in streams outside sensitive
natural production areas.

Integration of hatchery fish into wild stocks requires careful planning of the
number and size of fish stocked, and the areas and time of stocking. Streams
or reaches where natural spawning has been deficient are obvious choices for
consideration. Stocking the fish in a single location may produce satisfactory
results in small streams containing few wild fish (Elson 1957) or poor physical
habitat (Bilby and Bisson 1987). Elson (1957) reported that stocked Atlantic
salmon fry survived as well to smolt stage whether they were stocked in one
location or scattered over 1/2 mile of stream. For streams possessing better
quality habitat or significant wild fish populations, it is. recommended that
stocking sites be widely distributed to promote the equitable distribution of
juveniles into available habitat and to lessen competition (Wentworth and LaBar
1984; Kennedy and Strange 1978; Bilby and Bisson 1987). Resident fish are
less likely to be affected if stocking rates and locations are planned to exploit
unused food and habitat resources without exceeding the carrying capacity of
the stream.

Acknowledgernents

Funding for this review of published literature was provided by the Office of
Information Transfer and the Dworshak Fisheries Assistance Office of the U.S.
Fish and Wildlife Service, with funds from the Bonneville Power Administration.
Contribution No. 526 of Forest, Wildlife, and Range Experiment Station,
University of Idaho.

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126

TECHNICAL REPORT 90-2

CONCEPTS FOR A MODEL TO EVALUATE SUPPLEMENTATION

OF NATURAL SALMON AND STEELHEAD STOCKS

WITH HATCHERY FISH,

T.C. Bjornn and C.R. Steward

Idaho Cooperative Fish and Wildlife Research Unit
University of Idaho, Moscow, Idaho

for

Dworshak Fisheries Assistance Office
U.S. Fish and Wildlife Service
Ahasaka, Idaho

and

Bonneville Power Administration
Portland, Oregon

1990

Preface

Three reports were prepared for the BPA project:

1 .Analysis of Salmon and Steelhead Sur)121ementation: Emphasis on
Unpublished Rel2orts and Present Programs, by W.H. Miller, T.C.
Coley, H.L. Burge, and T.T. Kisanuki.

2. Supplementation of Salmon and Steelhead Stocks with Hatchery
Fish: A Synthesis of Published Literature, by C.R. Steward and
T.C. Bjornn.

3. Concepts for a Model to Evaluate Sugplementation of Natural
Salmon and Steelhead Stocks with Hatchery Fish, by T.C. Bjornn
and C.R. Steward.

Abstract.-Concepts and the basic components for a model that
could be used to evaluate supplementation of native or naturally
produced salmon and steelhead stocks with hatchery fish are
presented and discussed with an example of a model in
spreadsheet form. The example we developed, and the final
model should be similar in form and function to the life-history
model being used for system planning by the Northwest Power
Planning Council, except that additional genetic groups of fish
must be tracked through multiple generations. The number of
genetic groups monitored should be held to less than 10, we
suggest 6. Coefficients used for the system planning model will
provide a basis for selecting coefficients for individual stocks.
Managers should participate in determining the level of
resolution desired from the model and the range of values for
coefficients.

Supplementation of native stocks of salmon and steelhead with hatchery fish
has occurred, and will occur more frequently in the Columbia River drainage
with increased efforts to increase the size of the fish runs. The benefits and
costs associated with supplementation are not easily assessed, in part because
of our incomplete knowledge of the outcome of the many interactions that can
occur between native and hatchery fish (see reviews by Miller et al 1990 and
Steward and Bjornn 1990). There are numerous examples of large numbers of
adult salmon and steelhead being produced from hatchery operations. In some
cases, however, hatchery fish have been shown to be less fit in natural
systems than the local native fish (Reisenbichler and McIntyre 1977; Chilcote
et al. 1986), leading to offspring of native X hatchery crosses that may have
reduced fitness (Kapuscinski and Lannan 1986) relative to native fish. The
challenge is to maintain or improve the genetic quality of hatchery fish and
determine the best ways to use natural and hatchery production to increase the
abundance of anadromous fish in the Columbia River basin.

There are a number of terms used to describe groups of salmon and
steelhead. Listed below are our definitions of most of the terms and their use
in this report:

Species: a taxonomic unit that may be further divided into subspecies,
races, demes, or stocks. Examples, chinook salmon Oncorhynchus
tschawytscha, and steelhead Oncorhynchus mykiss.

Subspecies, race, deme, and stock: terms that we use synonymously to
identify groups of fish that are reproductively isolated in space or time
and that may have developed a unique genome. We prefer the term
stock. Examples, the Lemfii River stock of the spring-run of Columbia
River chinook salmon, and the Grande Rhonde stock of group-A
steelhead.

Population and run: terms used to describe a group of fish usually of the
same species that are together in a specific time or place. Examples,
the spring-run of chinook salmon and the group-A run of steelhead as

they migrate up the Columbia River, and a population of juveniles in a
stream or in the ocean. Note that populations or runs may be made up
of individuals from one or more stocks.

Native, indigenous, and endemic: terms often used synonymously to
identify the groups of fish that naturally colonized stream or lake
systems and were present when man began to alter the habitat and
biota of the Columbia River drainage in the 19th and 20th centuries.
Examples, the native Warm River stock(s) (Deschutes River tributary) of
spring-run chinook salmon, and the native upper Snake River stock of
fall-run chinook salmon. We prefer and will use the term native when
we wish to identify naturally produced fish of indigenous stock
ancestry.

Wild and natural: terms used to identify fish that have been naturally
produced (parents spawned naturally and fish grew up in streams or
lakes and eventually the ocean) without regard to ancestry (native or
alien or hatchery stock). The term wild is often used synonymously
with native, and for that reason we will avoid use of the term wild, and
use the term natural to describe naturally produced fish where that is
the only distinction we wish to make, or where we are unsure of
ancestry. Examples, the natural steelhead in the South Fork of the
Clearwater River that may be offspring of: (1) adults from prior releases
of hatchery smolts, (2) hatchery adults released to spawn naturally, or
(3) crosses of hatchery and natural adults.

Hatchery: a term we will apply to fish that have spent any part of their life
in a hatchery. On one end of the spectrum of hatchery fish is a fish
that resulted from gametes taken from native parents, incubated in a
hatchery only to the eyed-stage, and then placed back in its stream to
complete its life cycle. The other extreme could be a hatchery program
started with an alien stock where the fish were selected to perform best
in the given hatchery environment or to meet other management goals,
the fish are reared in the hatchery till the smolt stage, adults return to
the hatchery, and the program has continued for many generations.
Examples, steelhead returning to the Lochsa River that originally were
stocked in the stream as fry or as smolts would be hatchery adults,
perhaps with different abilities to produce viable offspring, but still
hatchery fish as we define them.

To supplement the native stocks of salmon and steelhead with hatchery fish
is to add production to, or make up for a deficiency in production of native fish.
In general, the goal is to produce more adult fish that will be available in
fisheries in preferred areas. More adults can be produced by more fully using
the capacity of freshwater production areas (reduce the deficiency), and by
releasing smolts to exceed that capacity (add production to that naturally
possible). Natural production in freshwater could be limited in various habitats
and life stages; the number of fry produced may be limited by the amount and
quality of spawning and incubation areas rather than by the number of
spawners, the number of smolts produced could be limited by habitat used in
summer by feeding juveniles or by habitat used in winter by juveniles seeking
security. If production by the native fish is significantly below the carrying
capacity of the environment because there are too few spawners or too few
juveniles produced, then supplementation by stocking hatchery adults, eggs,

fry, or sub-smolts should increase the number of smolts produced.
Supplementation by stocking smolts could insure full use of the natural
production capacity and could result in more adults produced than would be
possible with full natural production because the number of hatchery smolts
stocked is constrained by hatchery capacity and not the carrying capacity of a
stream system.

Unfortunately, supplementation is not simply an additive process whereby
the number of fish produced is equal to the normal native production plus the
hatchery fish stocked. For the species that spend months or years in
freshwater before going to the ocean, hatchery juveniles (and naturally
produced offspring of hatchery origin) will compete with and displace some
native juveniles. The number of fish displaced will depend on the proportion of
the capacity that is unused, abundance of native fish, number of hatchery fish
stocked or produced from hatchery adults, the size and time of stocking, and
fitness (relative measure of adaptation to a particular environment) of the
hatchery fish.

If there is little or no difference in fitness and other important characteristics
between the stock of fish to be supplemented and the hatchery stock, then
displacement of the native fish may be of little consequence. If there are
differences between the native and hatchery fish, however, then
supplementation may lead to reduced production of native fish, an overall
reduced fitness of naturally produced fish, and less production of adults than
anticipated.

A modelling approach to assessing the long-term effects of supplementation
on genetic makeup and productivity of salmon and steelhead stocks has utility
because the field studies to evaluate supplementation will be difficult to
conduct (replication and length of time). Concepts, factors, and variables that
should be included in a multi-generation, multi-genetic group model that can be
used to predict the outcome and evaluate various supplementation scenarios
are presented below. A discussion should be held with managers to decide
which variables to include in a model and the degree of stock definition that is
necessary.

Concepts for Consideration

Factors to Include in a Model

There are many factors that are explicitly or implicitly expressed in a life-
history type model that can be used to predict and evaluate the effects of
supplementation. Some factors are labelled and readily recognized in the
model, but some are expressed through a coefficient or relation used to link
components of the model. The following is a listing of factors that should be
considered for inclusion in a model for evaluating supplementation.

A- Life history stages:

Spawner to eggs deposited,
Eggs to fry that emerge,
Fry to parr produced,
Parr to smolts produced,

Smolts to recruits, and
Recruits to spawners.

13- Types of fish:

Species of fish,
Native, endemic, or indigenous,
Naturally produced (wild) from native, hatchery, or mixed parents,
Hatchery fish.

C- Stock parameters:

Age structure,
Proportion females,
Eggs per female,
Survival rates and relations for each life stage,

D- Genetic factors:

Relative fitness of hatchery versus wild or native fish,
Rate of change in fitness over time in hatchery and streams,
Origin and history of hatchery broodstock,
Frequency of wild fish addition to hatchery broodstock,
Intensity of selection in the hatchery and natural environment,
Effective population size,
Gene flow between wild and hatchery stocks, and
Definition of a genetically distinct group,

E- Environment of the stocks:

Quality and quantity of habitat,
Presence of other species that are competitors or predators,
Carrying capacity for each life stage,
Recent changes in environment that affect genome of native fish,
Variability of factors affecting survival,

F- Supplementation methods:

Life stage of fish stocked,
Proportion of area stocked,
Duration of stocking,
Size and number of stocked fish relative to natural fish,
Time and method of release of hatchery fish,
Number of sub-smolts stocked relative to carrying capacity, and
Number of smolts stocked relative to carrying capacity.

G- Interactions between hatchery and wild or native fish:

Mating overlap in time and space,
Use of summer and winter habitat by juveniles,
Competition for food and space,
Predator-prey interactions,
Transmission of disease,

Alteration of fishing patterns and harvest rates,
Response of wild or native fish to hatchery fish, and
Differences in behavior of wild versus hatchery fish.

The relative importance of the various factors and variables listed above can
only be estimated at -the present time because of the lack of definitive data.
Once a model has been constructed, sensitivity testing can be undertaken to
determine which factors and interactions have the largest potential for
changing the number and type of fish produced. For example, we suspect that
releasing smolts will result in more adults returning and more interactions with
native fish than if fry were stocked, but the outcome of the interactions depend
on the fitness of the hatchery fish, number stocked, size of fish stocked, time
of stocking, etc. and cannot be estimated easily without a model.

The reliability of the coefficients that are needed to run a model to evaluate
supplementation strategies is fair, at best, but can be estimated with enough
accuracy to use a model and feel confident that the predicted outcomes are
likely within the 'ballpark', and certainly useful for relative comparisons.
Attempting to operate the model will quickly reveal where there is little or no
empirical data to use in developing values for the necessary coefficients, and
thereby identify where research is needed.

The life history model that we propose herein can be illustrated as a series of
linked relations that define the number of fish produced at each life stage
(Figure 1). All of the variables that affect the production of fish and are to be
included in the model must be expressed as a coefficient incorporated into one
or more of the linked relations. For example, if hatchery fish produced
offspring that were less likely to survive than wild fish because they spawned
at a less optimum time, the fitness coefficient in the egg to fry life-stage
relation should reduce the slope of the line in the relation and the number of fry
produced.

Groups to Follow in the Model

The number of groups of fish of various genetic ancestries can become large
when there is mating overlap and interbreeding between hatchery and native
fish and the offspring are followed for more than a few generations. For
example, if we started in generation 0 with spawning. by native adults (NO),
and a release of hatchery fry at the time progeny from the No spawners
entered the stream, there would be two groups of spawners at the next
generation (Nj and H-1), assuming the hatchery fish survived and returned as
adults. With continued stocking of fry, and interbreeding between the various
genetic groups, there would be four groups by the generation 2, 11 by the
third, 67 by the fourth (Table 1), 2,271 by the fifth, and 2,577,585 by the
sixth (Figure 2). The -foregoing numbers were calculated with sex of the native
or hatchery fish ignored in interbreeding. If sex and genetic ancestry must be
considered in the ma 'tings, the number of groups at each generation would be
nearly double those presented.

Eggs

Spawners

Wild
3:: Fry
a-Itc h ery
V) Recruits Eggs

:3
Parr

Smolts Fry

SM01ts:

Parr

Figure 1. The life-history relations that would be the primary components of a
model to evaluate strategies to supplement wild stocks of salmon and steelhead
with hatchery fish. The dashed line in the egg-to-fry relation illustrates how the
production of fry from hatchery spawners would be less than that from wild
spawners if the hatchery fish were less fit.

The foregoing numbers also assume that all fish resulting from a brood year
mature and spawn in the same year, which is not true. For example, adult
chinook salmon from a single brood year usually return in three subsequent
years after spending 1, 2, or 3 years in the ocean (Table 2). Steelhead adults
from a single brood year could return in as many as 7 subsequent years,
because they spend 1-4 years in fresh water before becoming smolts, and up
to 4 years in the ocean (Table 3). If we tried to keep track of the groups
resulting from interbreeding, by sex of spawners, and by the age of the
spawners, the number of groups would be larger still.

In our opinion, it is not necessary to follow each and every group that could
be identified through a number of generations in order to evaluate the
outcomes of supplementation. Our present knowledge of the fitness of
W
_1 I <d
c

offspring of hatchery or native X hatchery crosses would not allow us to
distinguish between anything but general groups. The primary issues of

general overall fitness, changes in fitness over time, and the number of fish
with reduced fitness can be monitored and evaluated if the offspring from given
matings were placed into general groups based on initial fitness generation, and
then followed as a groups over time.

To illustrate the general grouping than might be undertaken, we have
combined all of the genetic groups in Table 1 into six groups with viabilities of
0.50-0.59, 0.60-0.69, 0.70-0.79, 0.80-0.89, 0.90-0-99. and 1.00. Groups
would be assigned a fitness equal to the mid-point of the range. The frequency
distribution of the groups listed in Table 1 would be as listed in Table 4 when
grouped into the general groups described above. With different assumptions
from those used in preparing Table 1, the frequency distribution would change,
as illustrated for the case where the gap in hatchery-native fish fitness is
reduced by one-fourth with each generation of natural spawning and rearing
(Table 4). The important point is that the number of groups is reduced to a
manageable number.

The general functioning of a model to monitor supplementation results, with
fitness groupings, is illustrated in the spreadsheet depicted in Table 5. Native
fish in a particular drainage are assigned a fitness of 1.0 on a relative scale,
and the fitness of hatchery fish at first natural spawning must be estimated. If
only native fish were present, only the native column in the spreadsheet would
be used because the fitness would always be 1.0. If hatchery fish with a
fitness of less than 1.0 are added to the drainage, then other columns in the
spreadsheet would be used. In the example presented in the Table 5
spreadsheet, hatchery fry equal in number to the initial number of native fry
were added each year starting in generation 1.

When adults from the stocking of hatchery fry return to spawn they are
placed in fitness groups based on their fitness and on the fitness of the fish
they may mate with; sibling hatchery fish and native fish were the only options
in generation 2 of the example. We assigned a fitness of 0.55 to the returning
hatchery adults. If they mated with siblings, their offspring would have a
fitness of (0.55+0.55)/2 = 0.55. If they mated with native fish, their
offspring would have a fitness of (1.0+0.55)/2 = 0.775.

The number of adults involved in each type of mating (native X hatchery,
etc.) depends on the number of adults in each group and the amount of mating
overlap (full overlap in our example). At the end of generation 1, there were
1214 adults produced, 821 (67.63%) native adults and 393 (32.37%) adults
from the stocking of hatchery fry. The number of native X native matings
equal (0.6763 *0.6763) * 1214 = 555 spawners placed at the top of the native
fish column of the spreadsheet for generation 2. The number of hatchery X
hatchery matings equal (0.3237*0.3237)*1214 = 127 spawners placed in the
fitness group 0.55 column. The number of hatchery X native matings equals
(0.3237*0.6763)*1214 = 532 spawners placed in the fitness group 0.75
column. Sex ratios for native and hatchery fish were similar.

Fitness values for each life stage of the fish represented in the model, must be
set so that the product of the individual values is equal to the overall fitness
(spawners to adult progeny) value for the group (0.55, 0.65, etc.). In the
example, we selected values for each stage that

Table 1. List of groups of adults available to spawn and their relative fitness in each generation
with native (N) and hatchery (H) fish spawning in the first generation. Fitness of native fish
1.0, first generation hatchery spawners = 0.5 'and the gap in fitness between native and
hatchery fish, or their crosses, is reduced by half with each generation of natural reproduction.

Generations Generations
Genetic groups 1 2 3 4

Generation 1
Nj 1.00
0.50

Generation 2
N2 1.00
H12 0.75
H21 0.50
Nj XH11 0.88

Generation 3
N3 1.00
H13 0.88
H22 0.75
(Nj X Hl 1)2 0.94
N2 X H12 0.94
N2 X H21 0.88
N2 X (Nj X Hl 1) 0.97
H1 2 X H21 0.81
H12 X (Nj X Hl 1) 0.91
H21 X (Nj X Hl 1) 0.84
H31 0.50

Generation 4
N4 1.00
H14 0.04
H23 0.88
(Nj X Hl 1)3 0.97
(Nj X H12)2 0.97
(N2 X H21)2 0.94
(N2 X (Nj X Hl 1))2 0.98
(H 12 X H21)2 0.91
(1-112 X (Nj X Hl 1)2 0.95
(1-121 X (Nj X Hl 1))2 0.92
H32 0.75
N3 X H13 0.97
N3 X H22 0.94
N3 X (Nj X Hl 1)2 0.98
N3 X (N2 X H12) 0.98
N3 X (N2 X H21) 0.97
N3 X (N2 X (Nj X Hl 1)) 0.99
N3 X (H12 X H21) 0.95
N3 X (1-112 X (Nj X Hl 1)) 0.98

Table 1. continued

Generations Generations
Genetic groups 1 2 3 4

N3 X (H21 X (Nj X H1 1)) 0.96
N3 X H31 0.88
H13 X H22 0.91
H1 3 X (Nj X H1 1)2 0.95
H13 X (N2 X H12) 0.95
H13 X (N2 X H21) 0.94
HII 3 X (N2 X (Nj X H1 1)) 0.96
H13 X (H12 X H21) 0.92
H13 X (H1 2 X (Nj X H1 1)) 0.95
H1 3 X (H21 X (Nj X H1 1)) 0.93
H13 X H31 0.84
H22 X (Nj X H1 1)2 0.92
H22 X (N2 X H12) 0.92
H22 X (N2 X H21) 0.91
H22 X (N2 X (Nj X H1 1)) 0.93
H22 X (H12 X H21) 0.89
H22 X (H1 2 X (Nj X H1 1)) 0.91
H22 X (H21 X (N 1 X H 11)) 0.90
H22 X H31 0.81
(N 1 X H1 1)2 X (N2 X HII 2) 0.97
(N 1 X H1 1)2 X (N2 X H21) 0.95
(N 1 X H1 1)2 X (N2 X (Nj X H1 1)) 0.98
(N 1 X H1 1)2 X (H12 X H21) 0.94
(N 1 X H1 1)2 X (HII 2 X (Nj X H1 1)) 0.96
(N 1 X H1 1)2 X (H21 X (Nj X H1 1)) 0.95
(N 1 X H1 1)2 X H31 0.86
(N2 X H12) X (N2 X H21) 0.95
(N2 X H12) X (N2 X (Nj X H1 1)) 0.98
(N2 X HII 2) X (H1 2 X H21) 0.94
(N2 X H1 2) X (H1 2 X (Nj X H1 1)) 0.96
(N2 X H12) X (H21 X (Nj X H1 1)) 0.95
(N2 X H12) X H31 0.86
(N2 X H21) X (N2 X (Nj X Hl 1)) 0.96
(N2 X H21) X (H12 X H21) 0.92
(N2 X H21) X (H12 X (Nj X H1 1)) 0.95
(N2 X H21) X (H21 X (Nj X H1 1)) 0.93
(N2 X H21) X H31 0.84
(N2 X (Nj X H1 1)) X (H12 X H21) 0.95
(N2 X (Nj X H1 1)) X (H1 2 X (Nj X Hl 1)) 0.97
(N2 X (Nj X H1 1)) X (H21 X (Nj X Hl 1)) 0.95
(N2 X (Nj X H1 1)) X H31 0.87
(H1 2 X H21) X (HII 2 X (Nj X Hl 1)) 0.93
(H1 2 X H21) X (H21 X (Nj X H1 1)) 0.91
(H12 X H21) X H31 0.83
(H12 X (Nj X H1 1)) X (H21 X (Nj X H1 1)) 0.94
(H12 X (Nj X H1 1)) X H31 0.85
(H21 X (N 1 X H 11)) X H31 0.84
H41 0.50

2271

0 67

4
1 2

1 2 3 4 6
Generation

Figure 2. The number of genetic groups that would be present in each
generation, starting with only native fish spawning in the first generation,
hatchery adults spawning naturally at start of the second generation, and all
potential crosses occurring in subsequent generations. Sex and age at
spawning ignored.

represented our perception of where the largest fitness gap might exist.

In the spreadsheet example, we allowed fitness to increase by 10 units (from
0.55 to 0.65 for example) for each full generation of natural spawning and
rearing. Fish that originated as hatchery fish became the same as native fish in
terms of fitness when their combination of generations of natural reproduction
and matings with fish of higher fitness resulted in fitness values of 1.

Fitness of Native and Hatchery Fish

Differences in fitness, the ability to live and develop under normal conditions,
between native and hatchery fish can be large or small depending on the origin
of the hatchery stock, number of generations of domestication, and the type
and intensity of selection in the hatchery. For a given spawning and nursery
area, the native stock would have the highest fitness, the result of generations
of adaptation to environmental

Table 2. Examples of the age groups of chinook salmon that would contribute
to spawning runs from each brood year.

Years of return and age of adults
Brood year 1985 1986 1987 1988 1989 1990

Fall and some summer chinook salmon, age 0 smolts

1980 5
1981 4 5
1982 3 4 5
1983 2 3 4 5
1984 2 3 4 5
1985 2 3 4 5
1986 2 3 4
1987 2 3
1988 2

Spring and some summer chinook salmon, age 1 smolts

1980 6
1981 5 6
1982 4 5 6
1983 3 4 5 6
1984 3 4 5 6
1985 3 4 5 6
1986 3 4 5
1987 3 4
1988 3

conditions in the natal area and the migration paths. In areas where the
environment has been changed significantly, the fitness of native fish may be
reduced, but would still be higher than non-native stocks that might be
introduced, 'unless the environmental changes were so drastic that past
adaptations were of no value or were even maladaptive.

Hatchery stocks developed from the stock to be supplemented would likely
have the least difference in fitness, initially at least, from the native stock.
Theoretically, the size of the gap in fitness between the native stock and the
hatchery stock would depend on the type and severity of selection in the
hatchery, the frequency of native stock additions to the hatchery stock that
would improve the fitness of the hatchery stock, and the additions of hatchery
fish to the native stock that may lower the fitness of the native stock.
Hatchery stocks developed from nearby stocks with similar characteristics and
environments would appear to be next in preference to use of the local stock
for development of hatchery stocks used for supplementation because they
would likely have less difference in fitness than distant stocks from different
types of environments (Reisenbichler 1984).

Table 3. An example of the age groups of steelhead that could contribute
to spawning runs from each brood year, and the number of years in which
contributions would occur.

Brood year Years of return and age of adults
Smolt age 1986 1987 1988 1989 1990 1991 1992

1980
1 6
2 6 7
3 6 7 a
4 6 7 8 9
1981
1 5 6
2 5 6 7
3 5 6 7 8
4 6 7 8 9
1982
1 4 5 6
2 4 5 6 7
3 5 6 7 8
4 6 7 8 9
1983
1 3 4 5 6
2 4 5 6 7
3 5 6 7 8
4 6 7 8 9
1984
1 3 4 5 6
2 4 5 6 7
3 5 6 7 8
4 6 7 8
1985
1 3 4 5 6
2 4 5 6 7
3 5 6 7
4 6 7
1986
1 3 4 5 6
2 4 5 6
3 5 6
4 6
1987
3 4 5
2 4 5
3 5
4

Table 4. Frequency distribution of genetic groups by fitness groupings in
each generation from Table 1 with fitness of native fish = 1.0, first
generation hatchery spawners = 0.5, and the gap in fitness between native
and hatchery fish or their crosses reduced by half with each generation of
natural reproduction, and where the gap is reduced by one-fourth.

Generations Fitness range Gap reduced by Gap reduced by
Groups half (Table 1) one-fourth

Generation 1
Group 1 1.00 1 1
Group 2 0.90-0.99 0 0
Group 3 0.80-0.89 0 0
Group 4 0.70-0.79 0 0
Group 5 0.60-0.69 0 0
Group 6 0.50-0.59 1 1

Generation 2
Group 1 1.00 1 1
Group 2 0.90-0.99 0 0
Group 3 0.80-0.89 1 1
Group 4 0.70-0.79 1 0
Group'5 0.6o-6.69 .0 1
Group 6 0.50-0.59 1 1

Generation 3
Group 1 1.00 1 1
Group 2 0.90-0.99 4 1
Group 3 0.80-0.89 4 5
Group 4 0.70-0.79 1 2
Group 5 0.60-0.69 0 1
Group 6 0.50-0.59 1 1

Generation 4
Group 1 1.00 1 1
Group 2 0.90-0.99 52 10
Group 3 0.80-0.89 12 35
Group 4 0.70-0.79 1 17
Group 5 0.60-0.69 0 3
Group 6 0.50-0.59 1 1

To date, the difference in fitness between native or natural and hatchery
stocks of salmon and steelhead has been only partially assessed in a few cases
(Reisenbichler and McIntyre 1977; Chilcote et al. 1986). The results of these
studies have raised the concern about supplementing native stocks of fish with
hatchery stocks if the fitness of the hatchery fish is significantly less than the
native stock. In the examples we provide, we have assigned the native stock a
fitness of 1.0 and a lesser rate to the hatchery fish. The fitness of the progeny
of native X hatchery matings depends primarily on the fitness of the parents.

Table 5. An example of a spreadsheet model with life history stages and the necessary
coefficients for each stage to estimate the numbers of fish produced by each fitness group
in each generation.

Generation I
Parameters: Values Symbols B-H parameters
Proportion females 0.67 Pf
Eggs/female 6000 f
Egg-fry survival 0.5 Ef
Parr capacity 1000000 CP I.OOE-06 =aI
Parr prod rate 0.2 PO 5 -bI
Smolt capacity 500OW cs 2.OOE-06 --a2
Smolt prod rate 0.1 so 10 -b2
Smolt-rec survival 0.112 Sr
Recr-spawn survival 0.33 Ra

Natural fish fitness groups
Ufe stages Stociced
Variables Symbol Native hatchery 0.95 0.85 0.75 0.65 0.55 0.45 0.35

Spawners-"gs deposited
Number of spawners A 1000
Fitness-spawners Fs 1 1 0.98 0.97 0.96 0.95
Eggs deposited E 4020000 0 0 0 0 0 0 0 0

Eggs-fry emerged
Fftness-eggs Fe 1 0.99 0.98 0.96 0.95 0.9
Fry. emerged/stocked F 2010000 2010000 0 0 0 0 0 0 0

Fry-parr
Fitness-fry Ff 1 0.7 0.98 0.95 0.92 0.88 0.85
Adjusted fry number 2010000 1407000 0 0 0 0 0 0 0
Parr produced/stkd P 238W2 167162 0 0 0 0 0 0 0

Parr-smolt
Fftness-parr Fp 1 0.8 0.99 0.96 0.93 0.9 0.89
Adjusted parr number 238802 133729 0 0 0 0 0 0 0
Smolts produced/sM S 22224 12446 0 0 0 0 0 0 0

Smolt-recruit.
Fitness-smolts Fs 1 0.9 0.99 0.98 0.96 0.94 0.9
Adjusted smoft number 22224 11201 0 0 0 0 0 0 0
Recruits produced R 2489 1255 0 0 0 0 0 0 0

Recruft-spawner
Fitness-recrults Fr 1 0.95 1 0.99 0.98 0.97 0.94
Adjusted recruit no. 2489 1192 0 0 0 0 0 0 0
Spawners produced A 821 393 0 0 0 0 0 0 0

Relative overall fitness
Adult to adult 0.82 ERR ERR ERR ERR ERR ERR ERR
Fry to adult 0.0004 0.4788 ERR ERR ERR ERR ERR ERR ERR
Smolt to adult 0.0370 0.8550 ERR ERR ERR ERR ERR ERR ERR

Total smolts produced 33425 Percent native 66
Total adults produced 1215 Percent native 68

Table 5. Continued.

Generation 2
Parameters: Symbols B-H parameters
Proportion females 0.67 Pf
Eggstfemale 6000 f
Egg-try survival 0.5 Ef
Parr capacity 1DO0000 CP 1.OOE-06 -at
ParT prod rate 0.2 PO 5 =bI
SMOR capacity 500000 Cs 2.OOE-06 -a2
Smoh prod rate 0.1 so 10 =b2
Smoft-rec survival 0.112 Sr
Rea-spawn survival 0.33 Fla

Natural fish fitness groups
Ufe stages Stocked
Variables Symbol Native hatchery 0.95 0.85 0.75 0.65 0.55 0.45 0.35

Spawners-eggs deposited
Number of spawners A 555 0 0 532 0 127 0 0
Fftness-spawners Fs 1 1 0.98 0.97 0.96 0.95
Eggs deposited E 2232946 0 0 0 2074121 0 486307 0 0

Eggs-fry emerged
FlIness-eggs Fe 1 0.99 0.98 0.96 0.95 0.9
Fry emerged/stocked F 1116473 2010000 0 0 995578 0 218838 0 0

Fry-parr
Fitness-fry Ff 1 0.7 0.98 0.95 0.92 om 0.85
Adjusted fry number 1116473 1407000 0 0 915932 0 186012 0 0
Parr produoed/stkd P 129440 163123 0 0 106190 0 21566 0 0

Parr-smolt
Fitness-parr Fp 1 0.8 0.99 0.96 0.93 0.9 0.89
Adjusted parr number 129440 130498 0 0 98757 0 19193 0 0
Smolts produced/stkd S 12034 12133 0 0 9182 0 1784 0 0

Smolt-recrult
Fitness-smob Fs 1 0.9 0.99 0.98 0.96 0.93 0.9
Adjusted smolt number 12034 10920 0 0 8814 0 1606 0 0
Recruits produced R 1348 1223 0 0 987 0 180 0 0

Recruit- spawner
Fftness-;emlts Fr 1 0.95 1 0.99 0.98 0.97 0.94
Adjusted recrult no. 1348 M2 0 0 967 0 169 0 0
Spawners produced A 445 383 0 0 319 0 56 0 0

Relative overall fitness
Adult to adult 0.80 ERR ERR 0.75 ERR 0.55 ERR ERR
Fry to adult 0.0004 0.4788 ERR ERR 0.8049 ERR 0.6400 ERR ERR
Smoft to adult 0.0370 0.8550 ERR ERR 0.9408 ERR 0.8460 ERR ERR

Total smolts produced 33374 Percent native 36
Total adults produced 1203 Percent native 37

Table 5. Continued.

Generation 3
Parameters: Symbols B-H parameters
Proportion females 0.67 Pf
Eggstfemale 6000 f
Egg-fry survival 0.5 Ef
Parr capacity 1000000 Cp I.OOE-06 -al
Parr prod rate 0.2 PO 5 =b1
SMOR capacity 500000 Cs 2.OOE-06 -G2
Smoft prod rate 0.1 so 10 =b2
Smolt-rec survival 0.112 Sr
Recr-spawn survival 0.33 Ra

Natural fish fitness groups
Ufe stages Stocked
Variables Symbol Native hatchery 0.95 0.85 0.75 0.65 0.55 0.45 0.35

Spawners-eggs deposited
Number of spawners A 555 218 38 511 18 125 0 0
FlIness-spawners Fs 1 1 0.98 0.97 0.96 0.95
Eggs deposited E 2232946 0 876154 150060 1994430 70382 478591 0 0

Eggs-fry emerged
Fftness-eggs Fe 1 0.99 0.98 0.96 0.95 0.9
Fry emerged/stocked F 1116473 2010000 433696 73529 957327 33432 215366 0 0

Fry-parr
Fitness-try Ff 1 0.7 0.98 0.95 0.92 0.88 0.85
Adjusted fry number M6473 1407000 425022 69853 880740 29420 183061 0 0
Parr produced/stkd P 122534 154419 46646 7666 96662 3229 20091 0 0

Parr-smoft
Fftness-parr Fp 1 0.8 0.99 0.96 0.93 0.9 0.89
Adjusted parr number 122534 123535 46180 7360 89895 2906 17881 0 0
Smolts produced/stkd S 11324 11417 4268 680 8308 269 1653 0 0

Smolt--recruft
Fftness-smotts Fs 1 0.9 0.99 0.98 0.96 0.93 0.9
Adjusted smolt number 11324 10275 4225 667 7976 250 1487 0 0
Remits produced R 1268 1151 473 75 893 28 167 0 0

Recrult-spawner
Fhnes&-recruits Fr 1 0.95 1 0.99 0.98 0.97 0.94
Adjusted recruit no. 1268 1093 473 74 875 27 157 0 0
Spawners produced A 419 361 156 24 289 9 52 0 0

Relative overall fitness
Adult to adult 0.75 0.95 0.85 0.75 0.65 0.55 ERR ERR
Fry to adult 0.0004 0.4788 0.9605 0.8848 0.8049 0.7145 0.6400 ERR ERR
Srnoft to adult 0.0370 0.8556 0.9900 0.9702 0.9408 0.9021 0.8460 ERR ERR

Total smolts; produced 36203 Percent native 31
Total adults produced 1309 Percent native 32

Table 5. Continued.

Generation 4
Parameters: Symbols B-H parameters
Proportion females 0.67 Pf
Eggs/female 6000 f
Egg-try survival 0.5 Ef
Parr capacity 1000000 Cp 1.OOE-06 -at
Parr prod rate 0.2 PO 5 =b1
Smolt capacity 500000 Cs 2.OOE-06 -a2
Smolt prod rate 0.1 so JO -_b2
Smoft-rec survival 0.112 Sr
Recr-apawn survival 0.33 Ra

Natural fish fitness groups
Ufe stages Stocked
Variables Symbol Native hatchery 0.95 0.85 0.75 0.65 0.55 0.45 0.35

Spawners-eggs deposited
Number of spawners A 653 197 85 446 18 108 0 0
Fitness-spawners Fs 1 1 0.98 0.97 0.96 0.95
Eggs deposited E 2626764 0 790028 334620 1739676 70275 413849 0 0

Eggs-fry emerged
Fftness-eggs Fe 1 0.99 0.98 0.96 0.95 0.9
Fry emerged/stocked F 1313382 2010000 391064 163964 835044 33381 186232 0 0

Fry-parr
Fitness-fry Ff 1 0.7 0.98 0.95 0.92 0.88 0.85
Adjusted fry number 1313382 1407000 383243 155766 768241 29375 158297 0 0
Parr produced/stkd P 142522 152681 41588 16903 83366 3188 17178 0 0

Parr-smolt
Fitness-W Fp 1 0.8 0.99 0.96 0.93 0.9 0.89
Adjusted parr number 142522 122145 41172 16227 77530 2869 15288 0 0
Smolts produced/stkd S 13153 11273 3800 1498 7155 265 1411 0 0

Smolt-recrult
Fitness-smolts Fs 1 0.9 0.99 0.98 0.96 0.93 0.9
Adjusted smolt number 13153 10145 3762 1468 6869 246 1270 0 0
Recruits produced R U73 1136 421 164 769 28 142 0 0

Recrult-spawner
Fitness-recrults Fr 1 0.95 1 0.99 0.98 0.97 0.94
Adjusted recruit no. 1473 1079 421 163 754 27 134 0 0
Spawners produced A 486 356 139 54 249 9 44 0 0

Relative overall fitness
Adult to adult 0.74 0.95 0.85 0.75 0.65 0.55 ERR ERR
Fry to adult 0.0004 0.4788 0.9605 O.BM 0.8049 0.7145 0.6400 ERR ERR
Smolt to adult 0.0370 0.8550 0.9900 0.9702 0.9408 0.9021 0.8460 ERR ERR

Total smolts produced 36913 Percent native 36
Total adults produced 1337 Percent native 36

Table 5. Continued.

Generation 5
Parameters: Symbols B-H parameters
Proportion females 0.87 Pf
Eggs/female 6000 f
Egg-fry survival 0.5 Ef
Parr capacity 1000000 CP 1.00E-06 -at
Parr prod rate 0.2 PO 5 =bi
SMOR capacity 500000 Cs 2.OOE-06 -a
Smolt prod rate 0.1 so 10 =b2
Smoft-rec suMvgd 0.112 Sr
Recr-spawn survival 0.33 Ra

Natural fish fitness groups
Life stages Stocked
Variables Symbol Native hatchery 0.95 0.85 0.75 0.65 0.55 0.45 0.35

Spawners-eggs deposited
Number of spawners A 641 186 73 451 16 105 0 0
Fitness-spawners Fs 1 1 0.98 0.97 o.96 0.95
Eggs deposited E 2576365 0 747193 289301 1758214 80M 400228 0 0

Eggs-fry emerged
Fitness-eggs Fe 1 0.99 0.98 0.96 0.95 0.9
Fry emergedIstocked F 1288183 2010000 369861 141758 843943 28553 180103 0 0

Fry-pw
Fitness-fry Ff 1 0.7 0.98 0.95 0.92 0.88 0.85
Adjusted fry number 1288183 1407000 362463 134670 776427 25126 153087 0 0
Parr produced/stKd P 140832 153822 39627 14723 84884 2747 16736 0 0

Parr-smolt
Fitness-parr Fp 1 0.8 0.99 0.96 0.93 0.9 0.89
Adjusted parr number 140832 123057 39230 14134 78942 2472 14895 0 0
Smotts produce&stkd S 13007 11366 3623 1305 7291 228 1376 0 0

Smolt-fecruit
Fftness-smob Fs 1 0.9 0.99 0.98 0.96 0.93 0.9
Adjusted smolt number 13007 10229 3587 1279 6999 212 1238 0 0
Recruits produced R 1457 1146 402 143 784 24 139 0 0

Recrult-spawner
Fitness-recrults Fr 1 0.95 1 0.99 0.98 0.97 0.94
Adjusted recruit no. 1457 1088 402 142 768 23 130 0 a
Spawners produced A 481 359 133 47 254 8 43 0 0

Relative overall fitness
Adult to adult 0.75 0.95 0.85 0.75 0.65 0.55 ERR ERR
Fry to adult 0.0004 0.4788 0.9605 0.8848 0.8049 0.7145 0.6400 ERR ERR
Smolt to adult 0.0370 0.85W 0.9900 0.9702 0.9408 0.9021 0.8460 ERR ERR

Total smolts produced 36553 Percent native 36
Total adults produced 1323 Percent native 36

Table 5. Continued.

Generation 6
Parameters: Symbols B-H parameters
Proportion females 0.67 Pf
Eggstfemale 6000 f
Egg-fry survival 0.5 Ef
Parr capacity 1000000 Cp 1.00E-06 -at
Parr prod rate 0.2 PO 5 =bI
Smoft capacity 500000 Cs 2.OOE-06 --a2
Smolt prod rate 0.1 so 10 =b2
Srnolt-rec survival 0.112 Sr
Recr-spawn survival 0.33 Ra

Natural fish fitness groups
We stages Stocked
Variables Symbol Native hatchery 0.95 0.85 0.75 0.65 0.55 0.45 0.35

Spawners-eggs deposited
Number of spawners A 638 186 71 455 15 1w 0 0
Fitness-spawners Fs 1 1 0.98 0.97 0.96 0.95
Eggs deposited E 2563737 0 749352 279013 1774354 58065 407612 0 0

Eggs-fry emerged
Fltness-eggs Fe 1 0.99 0.98 0.96 0.95 0.9
Fry emerged/stocked F 1281869 2010000 370929 136716 851690 27581 183425 0 0

Fry-parr
Fitness-fry Ff 1 0.7 0.98 0.95 0.92 0.88 0.85
Adjusted fry number 1281869 1407000 363510 129881 783555 24271 155911 0 0
Parr produced/stkd P 140156 153838 39745 14201 85672 2654 17047 0 0

Parr-smott
Fitness-parr Fp 1 0.8 0.99 0.96 0.93 0.9 0.89
Adjusted parr number 140156 123070 39348 13633 79675 2388 15172 0 0
Smolts produced/stkd S 12945 11367 3634 1259 7359 221 1401 0 0

Smolt-recrult
Fitness-smolts Fs 1 0.9 0.99 0.98 0.96 0.93 0.9
Adjusted smolt number 12945 10230 .3598 1234 7065 205 1261 0 0
Recruits produced R 1450 1146 403 138 791 23 141 0 0

Recrult-spawner
Fitness-49oruits Fr 1 0.95 1 0.99 0.98 0.97 0.94
Adjusted recruit no. 1450 1089 403 137 775 22 133 0 0
Spawners produced A 478 359 133 45 256 7 44 0 0

Relative overall fitness
Adult to adult 0.75 0.95 - 0.85 0.75 0.65 0.55 ERR ERR
Fry to adult O.DO04 0.4788 0.9605 0.8848 0.8049 0.7145 0.6400 ERR ERR
Smoft to adult 0.0370 0.8550 0.9900 0.9702 0.9408 0.9021 0.8460 ERR ERR

Total smolts produced 36538 Percent native 35
Total adults produced 1323 Percent native 36

Changes in Fitness over Time

If the fitness of hatchery fish used to supplement a native stock is less than
the native fish, then one of the questions that arises is the rate at which the
fitness of natural progeny of hatchery fish (or crosses) converges on the fitness
of native fish. Theoretically, with each succeeding generation that progeny of
hatchery fish reproduce naturally their fitness should increase through natural
selection (Figure 3).

In the example provided in Table 1, we assumed that half the gap in fitness
between native fish and hatchery or crosses with hatchery fish had been closed
with each generation completed in the natural environment. Thus hatchery fry
stocked in the example and returning to spawn as adults (group H1 1 in Table
1) had a fitness of 0.5 at the start of the first generation, a fitness of 0.75
(group H 12) at the start of the second generation if they were the progeny. of a
H1 1 X H1 1 mating, a fitness of 0.88 (group H13) at the start of the third
generation if they were the progeny of a H 12 X H 12 mating, and a fitness of
0.94 (group H1 4) at thestart of generation 4 if they were the progeny of a H 13
X H 13 mating. In a model to evaluate supplementation, a procedure to adjust
the fitness coefficients (overall and for each life stage) must be included to
account for changes due to cross breeding, repeated natural reproduction, and
changes that may occur in the hatchery stock.

Operational Time Frame for Model

Models to evaluate supplementation could be set up to operate on year-to-
year or generation-to-generation time frames. If it were important to track the
contribution of each age group in every brood year, then the year by year
approach would be necessary. If we can assume, for modeling purposes, a
relatively constant age and sex ratio at maturity, a generation-to-generation
model could, be used. The model should probably be able to monitor all groups
for 20 or more generations, to allow ample time to reach equilibrium levels for
given conditions, and the opportunity to evaluate mid period changes in
conditions.

Life-Stage Compartments of Model

A life-history type model appears to be the most logical approach to
estimating the abundance of salmon and steelhead resulting from
supplementation, because hatchery fish of more than one life stage will be
added to streams. Relations can be developed for each of the life stages to
allow estimation of fish numbers of each type (native, hatchery, and those from
each fitness group) at each stage and to incorporate the effects of various
conditions through stage-specific coefficients, including those for fitness. With
life stage modeling, an assessment of the effects of supplementation can be
made for any stage, including number of fish produced and overall fitness.

1 W X W
......................... . .A

0.9-

H X W
F@ X H,
0.8- mate with sibs

V)
V)
LLJ
27- 0.7-
Keep mating with
LL- first generation hatchery

0.6 -

0.5-

0.4- -T-
1 2 3 4 5 6
GENERATIONS

Figure 3. Examples of fitness values for fish with various genetic
backgrounds and changes over time depending on parentage and rate of
improvement in fitness with each succeeding generation of natural
reproduction. In this example, the assumptions are as listed for groups in
Table 1.

For the salmon and steelhead stocks of the Columbia River, the life cycle can
be divided into many stages, but the stages listed below are probably the ones
needed to evaluate supplementation:

1. Adult to del2osited egg: the stage that incorporates the number, sex
ratio, fecundity, and fitness of the spawners, mating overlap
between groups, and the limitation, if any, of available spawning area
in estimating the number of eggs deposited in redds by each group of
fish or type of mating. This would be the starting stage for all
naturally produced fish and the start when supplementation is done
with hatchery adults.

2. Del2osited egg to emergent fry: the stage that includes the number
\H

and fitness of the eggs deposited and quality of the redd environment
(survival rate) to estimate the number of fry of each group that
would emerge from the redds. The initial generation for hatchery fish

would start with this stage if supplementation was done with newly
fertilized or eyed eggs.

3. Fry to fingerling pre-smolt: the number and fitness of emergent-fry is
related to the carrying capacity, density dependent, and density
independent mortality factors of the environment to estimate the
number of fish that reach the fingerling pre-smolt (parr) stage. The
pre-smolt stage is a user defined point in the life cycle between
emergent fry and smolt, that would correspond with the time when
pre-smolts might be stocked to supplement the native stock. For
spring chinook salmon that migrate to the sea as yearlings in the
spring, a pre-smolt stage might be the middle or end of the first
summer. For steelhead, it might be the end of the first, second, or
@third summer, depending primarily on the time pre-smolts are stocked
and on the age of fish at smolting. When supplementation is done
with fry, this stage would be the start of the initial generation for the
hatchery fish.

4. Pre-smolt to smolt: the stage that is created to facilitate evaluation of
supplementation with pre-smolts. It is necessary to estimate the
number of naturally produced pre-smolts produced so that a
comparison with hatchery pre-smolts can be made. The number and
fitness of the pre-smolts must be related to the carrying capacity and
mortality factors in the environment.

5. Smolt to recruit: the stage that includes the number and fitness of
natural and hatchery (if stocked) smolts, mortality rates during the
seaward migration, and mortality at sea up to 'the time the fish are
first recruited to the fisheries. If smolts are used for
supplementation, this stage would be the start of the initial hatchery
generation.

6. Recruit to sgawner: the periods from first recruitment to the fisheries,
migration upstream to the spawning areas, and the holding time prior
to spawning are included in this stage.

The relations for each of the life stages would be based on information
available from prior studies, or lacking that, on the judgement of experts. For
example, there is information available on the sex ratios, age composition, and
fecundity of many of the stocks of fish that would be supplemented and those
used for supplementing. Information on survival relations for each of the life
stages is not generally available, especially for each and every stock, but there
is enough information to make reasonable estimates of the relations. Relations
and coefficients used in the system planning model (Monitoring and Evaluation
Group 1989) developed by the Northwest Power Planning Council (NPPC) could
be used as a starting point.

Coefficients used to express the effects of fitness of the offspring of each
type of mating (native X native, hatchery X native, etc.), the amount of mating
overlap, and of such factors as size and health of fish used for supplementation
would be developed for each life stage (see example inTable 5 spreadsheet).
Native fish might be assigned a fitness coefficient of 1.0, for example, and
hatchery fish a lower value if less fit or a higher value if more fit for survival

than the native fish. Relative fitness of the hatchery fish or progeny of
hatchery X native matings may vary by life stage.

Incorporating survival relations for each of the life stages provides the
flexibility to take into account the special conditions that might be present in
spawning areas, streams used for rearing, river and reservoir migration routes,
and fisheries for each stock. For example, survival to

the smolt stage of spring chinook salmon rearing in headwater streams appears
to be a density-dependent asymptotic relation, whereas the relation for fall
chinook rearing in mainstem reservoirs could be a linear relation if density-
independpnt predation was the major cause of mortality.

Probability of Mating

The probability of mating between native and hatchery fish depends on the
number of native and hatchery adults, the sex ratio of both groups, and the
degree of overlap in time and location of spawning. Other factors could affect
the probability of mating, such as size of fish, general health, and willingness to
compete for mates, but we have assumed such factors will be similar for both
native and hatchery fish.

If only native fish were present, then the probability of mating between two
native fish would be 1.0 X 1.0 = 1.0. If equal numbers of native and hatchery
fish were present, the age and sex ratios were equal for both groups, and there
was full overlap in time and location of spawning the probability for each of the
four possible matings would be 0.25 (example 2, Table 6). If all else stayed
equal, but the numbers of each group changed, to say, three-fourths native
females and one-fourth hatchery, the probabilities would change to 0.563 for
the NF X NIVI cross, 0. 188 for the NF X HIVI and HF X NIVI crosses, and 0.063
for the HF X HIVI cross (example 3, Table 6). As long as the sex ratios were
similar for each of the groups being considered, the proportion of the
population of males used in the calculations would be the same as for females.
It would not matter if there were more or less males than females, as long as
the ratio was the same for both groups.

If there were differences in the sex or age ratios between native and
hatchery groups, the probabilities of mating would be affected as illustrated in
example 4 in Table 6. In this example, native females continued to make up
75% of the females, but the sex ratio of the native fish was set at 0.667
females and 0.333 males, and that of hatchery fish at 0.5 females and 0.5
males. In the total population of males then, native fish made up 0.6 and
hatchery fish 0.4. The proportion of N X H crosses increased relative to
example 3, because there were more hatchery males available to spawn.

If the degree of overlap in time or location of spawning is less than complete,
the probabilities of N X H crosses decreases because the fish are not all
together when spawning occurs. In example 5 (Table 6), we setoverlap at
50%; only half of the native and hatchery fish were spawning at the same time
or place. The matings between native females and native males includes those
from the half of the population that did not spawn at the same time or place as
the hatchery fish (probability 0.375) and those from fish that had the
opportunity to mate with hatchery fish, but didn't because of chance (0.281).

Table 6. Probabilities of mating for native and hatchery fish with varying
degrees of overlap in spawning time and location.

Proportion in aroup Over- Non- Prob-
Example Female Male lap overlap abilities

1. All native or all hatchery fish (sex ratio unimportant)
NF X NM = 1.00 X 1.00 X 1.00 1.000
HF X HM = 1.00 X 1.00 X 1.00 1.000

2. Half native and half hatchery fish (equal sex ratio, full overlap)
NF X NM = 0.50 X 0.50 X 1.00 0.250
NF X HM. =0.50 X 0.50 X 1.00 0.250
HF X NM = 0.50 X 0.50 X 1.00 0.250
HF X HM = 0.50 X 0.50 X 1.00 0.250

3. Females: 3/4 native and 1/4 hatchery (sex ratio same, full overlap)
NF X NM = 0.75 X 0.75 X 1.00 0.563
NF X HM = 0.75 X 0.25 X 1.00 0.188
HF X NM = 0.25 X 0.75 X 1.00 0.188
H FX HM = 0.25 X 0.25 X 1.00 0.063

4. Females: 0.75 native and 0.25 hatchery, males: 0.6 native and 0.4
hatchery, (full overlap)
NF X NM = 0.75 X 0.60 X 1.00 0.450
NF X HM = 0.75 X 0.40 X 1.00 0.300
HF X NM = 0.25 X 0.60 X 1.00 0.150
HF X HM = 0.25 X 0.40 X 1.00 0.100

5. Females and males: 0.75 native and 0.25 hatchery (50% overlap)
NF X NM = 0.75 X 0.5 0.375

NF X NM = 0.75 X 0.75 X 0.50 0.281
NF X HM = 0.75 X 0.25 X 0.50 0.094
HF X NM = 0.25 X 0.75 X 0.50 0.094
HF X HM = 0.25 X 0.25 X 0.50 0.031

HF X HM = 0.25 X 0.5 0.125

6. Females and males: 0.75 native and 0.25 hatchery (10% overlap)
NF X NM = 0.75 X 0.9 0.675

NF X NM = 0.75 X 0.75 X 0.10 0.056
NF-X HM = 0.75 X 0.25 X 0.10 0.019
HF X NM = 0.25 X 0.75 X 0.10 0.019
HF X RM = 0.25 X 0.25 X 0.10 0.006

HF X HM = 0.25 X 0.9 0.225

Methods of Supplementation

The methods of supplementation will be dictated by each manager's
perception of the best way to increase production, and by the factors
regulating the availability of fish from hatcheries. Unless the native stock has
been reduced to low levels of abundance, the best way to minimize the
potential for genetic damage to the supplemented stock is to use the local
stock as the source for the hatchery stock, add native/natural fish to the
hatchery broodstock periodically, avoid hatchery practices that select for a
segment of the population, and do not overwhelm the native stock with
hatchery fish. Hatchery fish from a genetically sound supplementation program
should have higher fitness values than those from hatchery stocks that are not
so managed.

Hatchery fish at many life stages have been used to supplement or restore
salmon and steelhead populations. Adults from hatcheries have been released
in streams or spawning channels to spawn naturally, newly fertilized and eyed
eggs have been placed in streams or incubation

channels, unfed fry and other pre-smolt juveniles have been released in'streams
to continue rearing, and smolts have been released to migrate seaward and
then return to spawn in the stream of release. The model must accommodate
the addition of hatchery fish at all of these life stages, which is a reason for the
recommended life-stage compartments.

The size and health of hatchery fish relative to the natural fish, season and
location of supplementation, and the effect of other species on the hatchery
fish can be accounted for in the fitness coefficient. If the hatchery fish are
more vulnerable to predation or angling, or less able to secure favorable living
space than their native counterparts, the reduced survival could be expressed
in a lower fitness coefficient.

Supplementation and the Carrying Capacity of Streams

For all forms of supplementation where the hatchery fish are expected to
spend a significant period of time in the natural environment before spawning
or becoming a smolt, the concept of a carrying capacity for fish must be
considered. There may be a limited number of spawning sites in a stream or
lake shore. Most streams and perhaps some large rivers or reservoirs have an
upper limit on the number (or biomass) of fish that can be supported during the
summer. The winter carrying capacity of streams may be different than that in
summer because of the factors involved.

Carrying capacities become important for species like chinook and coho
salmon and steelhead that spend a significant period of time in streams before
migrating to the ocean. During the freshwater phase dens ity-dependent forms
of mortality limit the number of smolts that can be produced in a given natural
environment. If a habitat is fully seeded by native fish and hatchery fish are
added, there will be a reduction in the number of native smolts produced to
compensate for the number of hatchery fish that compete successfully and
become smolts. A more critical concern is the case where there is a relatively
small number of native fish, a large number of hatchery fish are added, and the

native fish become further depressed because of the added competition they
must endure.

In a supplementation model the number of native, hatchery, and other
.genetic types of smolts produced is a function of the initial numbers of each
type of fish, their relative fitness, and the carrying capacity of the environment.
Non-native fish can be equated to native fish by multiplying their abundance by
their fitness coefficients. This adjusted initial number of non-native fish would
then be added to the number of native fish to obtain the effective initial number
of fish at the beginning of a life stage. The number of native and non-native
fish produced at the end of the life stage would then be the total number
produced multiplied by the proportion of each type at the beginning.

Effects of Supplementation on Other Species

Hatchery fish released in a stream to supplement one species may affect
other species. To assess the effect of supplementation on non-target species
the model must be able to track each of the species of interest through each
life stage and generation, and there must be a way to express the results of the
interactions that occur between the species. The severity of the interaction
effect would depend on the degree of niche overlap between two or more
species, what factors limit production, and the abundance of the fish relative to
the carrying capacity. A coefficient could be attached to each of the relations
for each life stage to modify the survival rate according to the effect of
interspecific interactions.

Deterministic versus Stochastic Models

A deterministic model would be used to evaluate the effects of
supplementation without the confounding effects of environmental variability.
A stochastic model would be useful to determine if environmental variability
would affect the outcome of supplementation, or to determine the likelihood of
extermination of stocks with marginal levels of abundance.

General Model Structure

A model (as described above) to evaluate supplementation of salmon and
steelhead stocks could be designed and constructed on a computer
spreadsheet (as the preliminary example in Table 5), or it could be a model
constructed with program code in the manner of the system planning model. In
either case, the basic components (life stages) of the model would be similar to
those of the system planning model, but the model would differ in the need to
keep track of selected genetic groups over time. At present, the system
planning model used by the NPPC keeps track of hatchery and native fish
throughout their life cycle, but only for the first generation. A spreadsheet
model used by Byrne and Bjornn (1988) to evaluate supplementation for a
steelhead population was constructed to keep track of hatchery and native fish
for many generations, but all fish with a hatchery origin were combined in a
single group regardless of the length of time since coming from the hatchery.

The ultimate model to evaluate supplementation would be able to track each
genetic group generated by matings between native, hatchery, and hatchery X

native parents; with age and sex of spawners considered. With such a model,
we would have more than 5,000 groups to monitor by the sixth generation,
and more than 5 million by the seventh generation. We might be able to
program present-day computers to monitor that many groups, but we would
likely have trouble providing coefficients that would be sufficiently
discriminating for each of the groups. From a practical viewpoint, it is probably
not necessary to monitor a large number of genetic groups to adequately
assess the success of a supplementation program.

Outputs of the model must include the number of fish of each genetic group
at the end of each life stage for each generation.

Coefficients for Variables

The coefficients provided with the documentation for the NPPC's system
planning model (Monitoring and Evaluation Group 1989) are a good starting
point in providing values needed for a supplementation model. Additional
information has been developed for many of the subbasins in the Columbia
River drainage as part of the system planning process. It will probably be
necessary to develop stock specific coefficients, which may or may not be
readily available, for use in a supplementation model. The coefficients
developed for the system planning process will at least be helpful in selecting
coefficients that are reasonable and similar to those found or used for other
stocks of fish.

In addition to survival rates for each life stage, fitness values for each of the
genetic groups must be assigned as a modifier of the survival rates.
Unfortunately there are few measures of relative fitness for the various stocks
of native and hatchery salmon and steelhead. In most cases, the progeny of
hatchery or hatchery X native parents would likely have a fitness coefficient
equal to or less than 1.0 if native fish were assigned a value of 1.0.
Theoretically, the fitness values for the introduced fish could range from 0.0 to
larger than 1.0. There have been cases where introduced fish did not survive
and reproduce. Conceivably, excellent hatchery smolts could have a higher
fitness coefficient than native fish for the first generation, if for example, the
larger size they attained in the hatchery allowed them to survive at a higher
rate than native smolts. Such benefits would not continue into succeeding
generations when their offspring would be limited in the same ways as other
naturally produced fish. We have not discussed heterosis or the breakdown of
coadapted genetic systems that might affect fitness in complex ways, because
we do not know how they might operate or how to include them in the model
at this stage.

Recommendations

We recommend that a model be developed soon to help in the assessment of
the effects of supplementation of wild stocks of salmon and steelhead with
hatchery fish. The model could be developed to run as a spreadsheet program,
similar to the example we provided, or it could be developed as a stand alone
program similar to the sub-basin planning model, perhaps even a modification
of that model.

We recommend that meetings be held, as needed, with a group of managers
to review progress on model development, to determine the resolution required,
and to evaluate the coefficients used in the model. These meetings are needed
to insure that the model and its components meet the needs of the managers
and that the predictions are as close to reality as possible.

Once the model is functional, it should be distributed to those interested, it
should be used to conduct sensitivity tests, and various supplementation
senerios should be run on a comparative basis to provide estimates of the
relative outcomes of various management strategies.

Acknowledge ments

Contribution No. 527 of Forest, Wildlife, and Range Experiment Station,
University of Idaho.

References

Byrne, A., and T.C. Bjornn. 1988. An evaluation of supplementing wild stocks
of steelhead with hatchery fish using a life history model. Technical
Report 88-3, Idaho Cooperative Fish and Wildlife Research Unit, University
of Idaho, Moscow.

Chilcote, M.W., S.A. Leider, and J.J. Loch. 1986. Differential reproductive
success of hatchery and wild summer-run steelhead under natural
conditions. Transactions of the American Fisheries Society 115:726-735.

Kapuscinski, A.R.D., and J.E. Lannan. 1986. A conceptual genetic fitness
model for fisheries management. Canadian Journal of Fisheries and
Aquatic Sciences 43:1606-1616.

Monitoring and Evaluation Group. 1989. System planning model
documentation. Northwest Power Planning Council, Portland, Oregon.

Reisenbichler, R.R. 1984. Outplanting: potential for harmful genetic change in
naturally spawning salmonids. Pages 33-39 in J.M. Walton and D.B.
Houston, editors. Proceedings of the Olympic Wild Fish Conference.
Peninsula College, Port Angeles, Washington.

Reisenbichler, R.R., and J.D. McIntyre. 1977. Genetic differences and survival
of juvenile hatchery and wild steelhead trout, Salmo gairdneri. Journal of
the Fisheries Research Board of Canada 34:123-128.

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