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Allen A. Elser, Fish and Wildlife Biologist Supervisor
Robert C. McFarland, Fish and Wildlife Biologist
Dennis Schwehr, Fish and Wildlife Biologist
Montana Department of Fish and Game
TECHNICAL REPORT NO. 8
conducted by the
Water Resources Division
Montana Department of Natural Resources and Conservation
32 S. Ewing
He 1 ena, rn 596Dl
Bob Anderson, Project Administrator
Dave Lambert, Editor
for the
Old West Regional Commission
22B Hedden Empire Building
Billings, MT 59101
Kenneth A. Blackburn, Project Coordinator
July 1977
·'
1730 K Street, N. W.
Suite 426
The Old West Regional Commission is a Federal-State
partnership designed to solve regional economic
problems and stimulate orderly economic growth in
the states of Montana, Nebraska, North Dakota,
South Dakota and Wyoming. Established in 1972
under the Public Works and Economic Development
Act of 1965, it is one of seven identical commissions
throughout the country engaged in formulating and
carrying out coordinated action plans for regional
economic development.
COMMISSION MEMBERS
State Cochairman
Gov. Thomas L. Judge of Montana
Alternate: Dean Hart
Federal Cochairman
'George D. McCarthy
State Members
Gov. Edgar J. Herschler of Wyoming
Alternate: Steve F. Freudenthal
Gov. J. James Exon of Nebraska
Alternate: Jon H. Oberg
Gov. Arthur A. Link of North Dakota
Alternate: Woody Gagnon
Gov. Richard F. Kneip of South Dakota
Alternate: Theodore R. Muenster
COMMISSION OFFICES
201 Main Street
Suite D
Washington, D. C. 20006
202/967-3491
Rapid City, South Dakota 57701
605/348-6310
Suite 228
Heddon-Empire Building
Billings, Montana 59101
406/657-6665
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FOREWORD
The Old West Regional Commission wishes to express its appreciation for
this report to the Montana Department of Natural Resources and Conservation,
and more specifically to those Department staff members who participated
directly in the project and in preparation of various reports, to Dr. Kenneth A.
Blackburn of the Commission staff who coordinated the project, and to the
subcontractors who also participated. The Yellowstone Impact Study was one
of the first major projects funded by the Commission that was directed at
investigating the potential environmental impacts relating to energy develop-
ment. The Commission is pleased to have been a part of this important research.
George D. McCarthy
Federal Cochairman
FIGURES.
TABLES .
ABBREVIATIONS USED IN THIS REPORT.
PREFACE.
The River . .
The Conflict.
The Study ..
Acknowledgments
PART I. TONGUE RIVER FISHERY STUDY.
INTRODUCTION. .
Purpose. .
Study Area
METHODS . . ..
Study Area Delineation ..
Instream Flow Determination.
Sampling and Tagging ..
Shovelnose Sturgeon
Sauger .....
Channel Catfish .
Age and Growth . . . . .
Population Estimates ..
Water Temperature. . . .
Impacts of Water Withdrawals
EXISTING SITUATION ...... .
Faunal Zonation ..... .
Resident Fish Populations.
..
Species Distribution ........... .
Population Numbers and Species Composition.
Species Diversity .
Shovelnose Sturgeon .. .
Fish Size .... .
Population Estimate
Time of Spawning ..
Habitat Preference ..... .
Sampling and Tagging Studies.
iv
Vii
X
xiv
1
1
1
5
6
7
9
9
9
13
. 13
. 13
. 14
. 14
. 15
. 15
. 15
. 16
. 17
. 17
. 19
. 19
. 19
. 19
. 21 . .23
. 24
.26
. 34
. 35
. 37
42
Sauger. . . . . . . . . .
Fish Size ..... .
Population Estimates
Habitat Preference
Tagging Studies.
Channel Catfish .. .
Fish Size .... .
Catch Rates ... .
Tagging Studies ..
Instream Flow Requirements of Indicator Species
Passage and Spawning Flows ... .
Rearing Flows .......... .
Monthly Instream Flow Requirements
mPACTS OF WATER WITHDRAWALS . . . . ....
The Naturally Occurring Pattern of Low Flows.
Impacts of Increased Future Use . .
Projections of Future Use. . .
Impacts of Reduced Streamflow .. .
Impacts on Water Quality .... .
Other Limiting Factors ..... .
Limiting Factors Unrelated to Flow
SUf1MARY.
PART II. TONGUE RIVER RESERVOIR FISHERY STUDY.
INTRODUCTION . .
Purpose .. ·
Study Area.
METHODS .....
Sampling for Water Chemistry Analysis
Fish Sampling ....
Population Estimates.
Creel Census.
EXISTING SITUATION . .
Limnology ....
Fish Populations.
Hi story.
Sampling Results
Creel Census .....
IMPACTS OF WATER WITHDRAWALS
Projection of Future Use.
Impacts on the Reservoir Fishery.
S!JMMARY.
v
47
47
51
52
52
52
55
57
58
58
60
60
62
65
65
65
65
67
71
72
73
75
77
79
79
79
83
83
83
83
84
85
85
85
85
87
107
111
111
111
113
PART III. FOOD HABITS AND FORAGE FISH.
INTRODUCTION
Purpose
Scope ..
Study Area.
METHODS .....
Food Habits Analyses.
Forage Fish Survey.
EXISTING SITUATION .
Stomach Contents.
Sauger.
Burbot. . . .
Channel Catfish
Goldeye ..... .
Shovelnose Sturgeon
Flathead Chub .
Other Species .
Food Selection. . . .
Forage Fish Survey. . .
IMPACTS OF WATER WITHDRAWALS
Riffle Habitat ...
Slow-water Habitat.
SUMMARY.
APPENDIXES.
A. Projections of Future Use. . . . ./..
B. Tongue River Water Temperatures.
C. Taxonomy of Fish Species Encountered in these Studies ..
D. Taxonomy of Invertebrates Found in Fish Stomachs . . . . .
E. Average Body Volume of Major Organisms Found in Fish Stomachs.
F. Results of Food Habits Analyses of Sauger, Burbot,
Goldeye, Channel Catfish, and Shovelnose Sturgeon ...
G. Yellowstone Basin Forage Fish Reported by Brown (1971)
LITERATURE CITED. . . . . . . . . . . . . . . . . . . . . . . .
vi
115
117
117
117
118
119
119
120
121
121
121
123
123
126
126
131
131
131
132
137
137
138
141
143
145
153
157
159
161
163
171
173
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/
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1.
2.
Yellowstone River Basin.
Tongue River in Montana:
and sampling sections ..
3
major diversions, tributaries,
11
3. Longitudinal profile of the Tongue River in Montana. . . 12
4. Comparison of diversity indices for 1974 (6 runs) and 1975 (3 runs)
and combined fall sampling (9 runs) at each primary sampling
station on the Tongue River ...................... 25
5. Comparison of the Shannon-Weaver diversity indices for 1974
and 1975 fall fish sampling in the Tongue River and the
combined fall sampling at each of the primary sections
excluding fish that were less than 150 mm in length. . . . . 25
6. Comparison of the 1975 and 1976 shovelnose sturgeon fork
length frequencies (by percentage of catch) in the Tongue River. 27
7. Comparison of the fork length frequencies of shovelnose
sturgeon taken in the Tongue River with those taken in the
Yellowstone River at Intake in the spring of 1975. . . . . 28
8. Weight~frequency histogram of the shovelnose sturgeon collected
in the spring of 1975 in the Tongue River. . . . . . . . . . . . 30
9. Weight-frequency histogram of the shovelnose sturgeon
collected in the spring of 1976 in the Tongue River. . . .... 31
10. The length-weight relationship equation of all shovelnose
sturgeon collected in the spring of 1976 in the Tongue River ..... 33
11. Linear regression analysis of the 1~eight at tagging (before
spawning) compared with the weight at recapture (after
spawning) of shovelnose sturgeon in the Tongue River . . .... 35
12. Five-day average temperatures (°C) and discharges in
relation to the spawning activities of the shovelnose
sturgeon and sauger in the spring of 1975 in the Tongue River ..... 36
13. Five-day average temperatures (OC) and discharges in relation
to the spawning activities of the shovelnose sturgeon and
sauger in the spring of 1976 in the Tongue River ........... 38
vii
14. Comparison of the catch rates of shovelnose sturgeon with
the bottom profile of the river channel for one reach of
the Tongue River . . . . . . . . . . . . . . . . . . . .
15. Quadratic regression analysis of discharge
rates of shovelnose sturgeon in the Tongue
versus catch
River in the
.... 39
spring of 1975 ............. . . . . . . . . 41
16. Quadratic regression analysis of discharge
rates of shovelnose sturgeon in the Tongue
versus catch
River in the
spring of 1976 ............. . . . . . . . 41
17. Quadratic regression analysis of minimum and maximum water
temperatures versus catch rates of shovelnose sturgeon in
the Tongue River in the spring of 1975 . . . . . . . . ..... 43
18. Quadratic regression analysis of minimum and maximum
water temperatures versus catch rates of shovel nose
sturgeon in the Tongue River in the spring of 1976 .......... 43
19. Comparison of the linear regression analysis of the
weight at tagging versus the weight at recapture of
monel-and anchor-tagged sturgeon over the three years
of sampling in the Tongue River. . . . . . . . . . . . . ...... 45
20. Weight-frequency graph of sauger collected in the spring
spawning migration of 1976 in the Tongue River . . . . . ...... 49
21. Comparison of the age and length frequency of sauger
taken in the spring spawning migrations of 1976 in the
Tongue River . . . . . . . . . . . . . . . . . . . . . . . . . . 49
22. Length-weight relationship equation of all sauger collected
in the spring of 1976 in the Tongue River. . . . . . . .... 50
23. Plot of the quantity of sauger taken per interval of dis-
charge in the spring spawning migration of 1976 in the
Tongue River . . . . . . . . . . . . . . . . . . . . . . . . . . . . 53
24. Quadratic regression analysis of discharge versus catch
rates of sauger collected in the spring of 1976 in the
Tongue River . . . . . . . . . . . . . . . . . . . . . . 53
25. Plot of the quantity of sauger
and minimum water temperatures
Tongue River . . . . . . . . .
taken per interval of maximum
in the spring of 1976 in the
26. Quadratic regression analysis of maximum and minimum water
temperature versus catch rates of sauger taken in the spring
. . . . . 54
of 1976 in the Tongue River ...................... 54
viii
.,.
L
27.
28.
29.
30.
Wetted perimeter in relation to discharge for three
sections of the Tongue River, showing the inflection
point used to determine rearing flows ....... .
Life history periodicity and minimum flow recommend-
ations for selected species and projected flow values
for the Tongue River from the T&Y Diversion to the
mouth . . . . . . . . . . . . . .
Tongue River Reservoir, Montana, showing zones and
sampling stations. . . . . . . ....
Inflow and outflow of Tongue River at Tongue River
Reservoir compared with storage elevation of the
. . . . . 61
. . . . . 63
..... 80
reservoir from April 1g75 to October 1976. . . ......... 86
31. Length-frequency of northern pike captured in trap
nets, Tongue River Reservoir, 1974-76, expressed as
each size interval's percentage of the total sample.
32. Average length and length range of northern pike from
. 95
gill-net catches, Tongue River Reservoir, 1964-76 ........... 96
33. Average length and length range of walleyes from gill-
net catches, Tongue River Reservoir, 1966-76 ............. 98
34. Length frequency of walleyes captured in trap nets,
Tongue River Reservoir, 1974-76, expressed as each size
interval's percentage of the total sample .............. 99
35.
36.
Length-frequency distribution of white and black crappie
taken in trap nets, Tongue River Reservoir, 1975-76,
expressed as each size interval's percentage of the
total sample ................. .
Monthly distribution of fishing pressure, Tongue River
Reservoir, 1975-76 .............. .
37. Monthly distribution of species as determined by creel
.102
.108
census, Tongue River Reservoir, 1976 . . . . . . . ....... 110
ix
1. Description of major sampling sections, Tongue River .......... 13
2. Distribution of fishes in the Tongue River by zones,
1974 and 1975 ..... : ............. . • . • . . 20
3. Summary of electrofishing samples for the Tongue River,
fall 1974 and 1975, expressed as numbers of fish/km of stream ..... 22
4. Summary of age-class strength of smallmouth bass in the
Tongue River, 1974-76 . . . . . . . . . . . . . . ....... 23
5. Fork lengths of shovelnose sturgeon captured in the
Tongue River in 1975 and 1976 . . . . . . . . . . . . ........ 26
6. Weights of shovelnose sturgeon captured in the Tongue
River in 1975 and 1976. . . . . . . . . . ........ 29
7. Estimated number of shovelnose sturgeon per km of the
Tongue River, 1975 and 1976 . . . . . . . . . . . . . . ...... 34
8. Percentage and direction of shovelnose sturgeon movement
9.
for May, June, and July 1976 in the 1 ower Tongue River. . . . . . . . 46
Difference between place of tagging
shovelnose sturgeon from 1974-76 in
River, expressed as percentage ...
and recapture for
the lower Tongue
. . . . . . . . . 46
10. Summary of tagged shovelnose sturgeon from the Tongue
River returned by anglers, 1974-76. . . . . . . . . ........ 46
11. Age and mean length of sauger taken in the Tongue
River, spring 1976. . . . . . . . . . . . . . . . . ....... 48
12. Comparison of calculated growth of Tongue River sauger
with those from other northern waters (mm). . . . . . . . . 51
13. Estimated populations of sauger moving into the lower
Tongue River, spring 1976 . . . . . . . . . . . . ........ 51
14. Average lengths and weights of catfish taken in the
Tongue River in 1975 and 1976 . . . . . . . . . . ...... 55
15. Average length and range of lengths for each age group
of 231 channel catfish taken below T&Y Dam on the Tongue
River in the summer of 1975 ....................... 56
X
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16. Average length and range of lengths for each age
17.
18.
19.
20.
group of 106 channel catfish taken between T&Y Diversion
· and S-H Diversion on the Tongue River in the summer of
1975 ............ · ...................... 56
Average lengths and range of lengths for each age
group of 132 channel catfish taken in the lower
Tongue River in the fall of 1976 ..... .
Summary of angler returns of tagged channel catfish,
Tongue River, 1975-76 .............. .
Summary of historic flows (1931-1975) on the Tongue
River as related to recommended instream flows by
season. .
Predicted impacts of three agricultural development
levels on the flow of the Tongue River .....
. . . . . . . . . 57
. ........ 59
. . . . . . . . . . 66
........ 68
21. Summary of predicted impacts of three projected levels
of industrial development of Tongue River water ........ 70
22. Summary of warm-water fish plants in the Tongue River
Reservoir, 1963-75. . . . . . . . . . . . . . . . ........ 88
23. Summary of trap net catches by zone in the Tongue
River Reservoir, 1975 ......................... 89
24. Summary of trap net catches by zone in the Tongue
River Reservoir, 1976 . . . . ................. 90
25. Comparison of trap net catches: Tongue River
Reservoir, 1972-76 (expressed as numbers per net
night) ................................. 91
26.
27.
28.
29.
30.
Summary of gill net (bottom) sets in the Tongue
River Reservoir, 1964-76, expressed as numbers of
fish per net set. . . . . . . . . . . . . . . . . . . . . ...... 92
Catch statistics of 18 overnight gill net (bottom)
sets, Tongue River Reservoir, July 1975 and 1976 ............ 93
Average lengths and weights of northern pike
caught in trap nets in the Tongue River Reservoir,
1972-76 ..................... . . 94
Population estimates of northern pike determined
from trap net catches, Tongue River Reservoir, 1974-76. . 96
Summary of northern pike tag returns by year for
Tongue River ~eservoir, 1973-76. (Number in parentheses
is the percentage of total tagging.) .................. 97
xi
31. Average lengths and weights of walleye caught
in trap nets in the Tongue River Reservoir, 1972-76 .......... 99
32.
33.
34.
35.
36.
37.
38.
39.
40.
41.
42.
43.
44.
45.
46.
Summary of walleye and sauger tagging and returns,
Tongue River Reservoir, lg73-76. (Number in
parentheses is the percentage of total tagging.) .
Average lengths and weights of black and white crappie,
Tongue River Reservoir, April-May 1g75 ....... .
Population estimates of black and white crappie deter-
mined from trap net catches, Tongue River Reservoir,
1974-76 .................... .
Number of bass per 100 meters of shoreline, Tongue
River Reservoir, 1974-75 . . . . . . . . .
Back-calculated lengths (mm) of smallmouth bass,
Tongue River Reservoir, 1976 ...... .
Back-calculated lengths (mm) of largemouth bass,
Tongue River Reservoir, 1976 ...... .
Summary of smallmouth bass tagging and angler returns
by year, Tongue River Reservoir, lg73-76 ...... .
Summary of largemouth bass tagging and angler returns
by year, Tongue River Reservoir, 1974-76 .....
Miscellaneous statistics of Tongue River Reservoir
creel census, 1975-76 .............. .
Estimated angling effort and harvest of sport fish,
Tongue River Reservoir, 1975 and 1976 ....... .
Numbers, lengths, and weights of fish collected for
stomach analysis ............... .
Stomach contents of 43 sauger collected from the lower
Yellowstone River during 1975 and 1976 .....
Stomach contents of 13 burbot collected from the
Yellowstone River below Miles City in January 1976
Stomach contents of 20 channel catfish collected from
the Yellowstone River near Miles City and Intake and
from the mouth of the Tongue River from July through
September, 1975 and 1976 .............. .
Stomach contents of 17 goldeye collected from the
Yellowstone River at Miles City in August, 1975 and 1976
xii
. 100
. 103
. 103
. 105
. 105
. 106
. 106
. 106
.1 07
.1 09
.121
.122
.124
.125
.127
J
47. Stomach contents of 20 shovelnose sturgeon collected
from the Yellowstone River near Miles City and Intake
during May and June, 1975 and 1976 ......... . 128
48. Stomach contents of 21 shovelnose sturgeon collected from the
Yellowstone River below Intake from July to September, 1975 to 1976 129
49.
50.
51.
Food types of miscellaneous fish species ......... .
Ivlev's electivity index for benthic food organisms
eaten by shovelnose sturgeon, goldeye, and channel catfish.
Forage fish species list for lower Yellowstone River
showing location, date of collection, and habitat sampled .
xiii
130
131
133
af
af/y
b/d oc
cc
cfs
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DCA
DNRC
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fl
ft/sec
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in
kg
km
lb
m
mg/1
mi
ml
rran
rranaf /y
mmcfd ·
mmt/y
11M
m/sec
m3/sec
N
R
t/d
tl
WSP
acre-feet
acre-feet/year
barrels/day
degrees Celsius
cubic centimeters
cubic feet/second
confidence interval
species diversity index
Department of Community Affairs
Department of Natural Resources
and Conservation
electivity index
degrees Fahrenheit
fork 1 ength
feet/second
grams
hectares
cubic hectometers
inches
kilograms
kilometers
pounds
meters
milligrams per liter
miles
milliliters
mi 11 imeters
million acre-feet/year
million cubic feet per day
million tons/year
megawatts
meters/second
cubic meters/second
number
redundancy
tons/day
total length
Water Surface Profile
xiv
THE RIVER
The Yellowstone River Basin of southeastern r1ontana, northern Hyomi ng, !
and western North Dakota encompasses approximately 180,000 km2 (71 ,000 square J
miles), 92,200 (35,600) of them in r1ontana. Montana's portion of the basin
comprises 24 percent of the state's land; where the river crosses the
border into rlorth Dakota, it carries about 8.8 million acre-feet of water per
year, 21 percent of the state's average annual outflow. The mainstem of the
Yello~1stone rises in northwestern l~yoming and flows generally northeast to its
confluence with the Missouri River just east of the Mor1tana-North Dakota
border; the river flows through Montana for about 550 of its 680 miles. The
major tributaries, the Boulder, Stillwater, Clarks Fork, Bighorn, Tongue, and
Powder rivers, all flow in a northerly direction as shown in figure 1. The
~1estern part of the basin is part of the middle Rocky i~ountains physiographic
province; the eastern section is located in the northern Great Plains (Rocky
Mountain Association of Geologists 1972).
THE COflFLICT
Historically, agriculture has been Montana's most i~portant industry. In
1975, over 40 percent of the primary employment in Montana was provided by
agriculture (r1ontana Department of Community Affairs 1976). In 1973, a good
year for agriculture, the earnings of labor and proprietors involved in
a~ricultural production in the fourteen counties that approximate the
Yellowstone Basin were over Sl4l million, as opposed to $13 million for
mining and $55 million for manufacturing. Cash receipts for Montana's
agricultural products more than doubled from 1968 to 1973. Since that year,
receipts have declined because of unfavorable market conditions; some
improvement may be in sight, however. In 1970, over 75 percent of the
Yellowstone Basin's land was in agricultural use (State Conservation Needs
Committee 1970). Irrigated agriculture is the basin's largest 1·1ater use,
consuming annually about 1.5 million acre-feet (af) of water (Montana DNRC
1977).
There is another industry in the Yellowstone Basin \~hich, though it con-
sumes little 1~ater no~1. may require more in the future, and that is the coal
develop~ent industry. In 1971, the North Central Power Study (North Central
Power Study Coordinating Committee 1971) identified 42 potential power plant
sites in the five-state (~lantana, North and South Dakota, Uyoming, and
Colorado) northern Great Plains region, 21 of them in Montana. These plants,
all to be fired by northern Great Plains coal, would generate 200,000 megawatts
(mw) of electricity, consume 3.4 mill ion acre-feet per year (mmaf/y) of water,
and result in a lar9e population increase. Administrative, economic, legal,
l
and technological considerations have kept most of these conversion facilities,
identified in the North Central Power Studv as necessary for 1980, on the
drawing board or in the courtroom. There fs now no chance of their being
completed by that date or even soon after, which will delay and diminish the
economic benefits some basin residents had expected as a result of coal
development. On the other hand, contracts l1ave been signed for the mining
of large amounts of Montana coal, and applications have been approved not
only for new and expanded coal mines but also for Colstrip Units 3 and 4,
twin 700-mw, coal-fired, electric generating plants.
In 1975, over 22 million tons of coal were mined in the state, up from
14 million in 1974, 11 million in 1973, and 1 million in 1969. By 1980, even
if no new contracts are entered, Montana's annual coal production will exceed
40 million tons. Coal reserves, estimated at over 50 billion economically
strippable tons Ulontana Energy Aclvisory Council 1976), pose no serious con-
straint to the levels of development projected by this study, which range
from 186.7 to 462.8 million tons stripped in the basin annually by the year
2000. Strip mining itself involves little use of water. How i~portant the
energy industry beco~es as a water user in the basin will depend on: 1) how
much of the coal mined in Montana is exported, and by what means, and 2) by
what process and to what end product the remainder is converted within the
state. If conversion follows the patterns projected in this study, the energy
industry will use from 48,350 to 326,740 af of water annually by the year 2000.
A third consumptive use of water, municipal use, is also bound to
increase as the basin population increases in response to increased employment
opportunities in agriculture and the energy industry.
Can the Yellowstone River satisfy all of these demands for her water?
Perhaps in the mainstem. But the tributary basins, especially the Bighorn,
Tongue, and Pm~der, have much smaller flows, and it is in those basins that
much of the increased agricultural and industrial water demand is expected.
Some impacts could occur even in the mainstem. What 1~ould happen to
water quality after massive depletions? How would a chan9e in water quality
affect existing and future agricultural ,industrial, and municipal users?
\~hat would happen to fish, furbearers, and migratory waterfowl that are
dependent on a certain .level of instream flow? Would the river be as
attractive a place for recreation after dewatering?
One of the first manifestations of f·1ontana 's gro1~ing concern for water
in the Yellowstone Basin and elsewhere in the state was the passage of
significant legislation. The Hater Use Act of 1973, which, among other
things, mandates the adjudication of all existing water rights and makes
possible the reservation of ~later for future beneficial use, was followed
by the Hater Moratorium Act of 1974, 1·1hich delayed action on major
applications for Yellowstone 3asin water for three years. The moratorium,
by any standard a bold action, was prompted by a steadily increasing rush of
applications and filings for water (mostly for industrial use) which, in two
tributary basins to the Yellowstone, exceeded supply. The DNRC's intention
during the moratorium was to study the basin's water and related land
resources, as well as existing and future need for the basin's water, so that
2
YEllowsTONE RIVER BASIN.
0 10 20 40 60 80 100 Miles
UiJiJ I I I I I
0 10 20 40 60 80 100 Kilometers
m----1 I I I I
I MUSSELSHELL
I
WHEATLAND I
0
-------~-J VALLEY
0 ~----~-
L -li--"...........,-+-""""'
GOLDEN\
_j CARBON
0 rj ______ ,,
---+, _ __._
YELLOWSTONE ' )
NATIONAL PARK 0
(
N YELLOWSTONE
RIVER BASIN
GARFIELD
, ------L
\T REA s_,_u,.R ... E~-._:._
I
L--~ I COLSTRIP l--: --1 •
' ---------. r
~~
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McCONE
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ASHLAND INDIAN
I
BIG HORN
RESERVATION ~·
----r--r
l l ----~
\ Tongue Ri ... er ~ Reservoir
---~ --,__ __ _
~----~-~------~-
WYOMING
----,
I --l,
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DAWSON
,
GLENDIVE)
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the state would be able to proceed wisely with the allocation of that water.
The study 1~hich resulted in this series of reports was one of the fruits of
that intention. Several other Yellowstone water studies were undertaken
during the moratorium at the state and federal levels. Early in 1977, the
45th l·iontana Legislature extended the moratorium to allo~1 more time to con-
sider reservations of water for future use in the basin.
THE STUDY
The Yellowstone Impact Study, conducted by the Water Resources Division
of the Montana Department of Natural Resources and Conservation and financed
by the.Old West·Regional Commission, was designed to evaluate the potential
physical, biological, and water use impacts of water withdrawals and water
development on the middle and lower reaches of the Yellowstone River Basin in
Montana. The study's plan of operation was to project three possible levels
of future agricultural, industrial, and municipal development in the
Yellowstone Basin and the streamflow depletions associated with that develop-
ment. Impacts on river morphology and water quality were then assessed,
and, finally, the impacts of altered streamflow, morphology, and water
quality on such factors as migratory_ birds, furbearers, recreation, and
existing water users were analyzed.
The study began in the fall of 1974. By its conclusion in December of
1976, the information generated by the study had already been used for a
number of moratorium-related projects--the EIS on reservations of 1~ater in
the Yellowstone Basin,. for example (Montana DNRC 1976). The study resulted
in a final report summarizing all aspects of the study and in eleven
specialized technical reports:
Report No.-1
Report No. 2
Report No. 3
Report No. 4
Report No. 5
Report flo. 6
Report No. 7
·Futur-e. Development Projections and Hydrologic Modeling in
the Yellowstone River Basin, Montana.
The Effect of Altered Streamflow on the Hydrology and
Geomorphology of the Yellowstone River Basin, t•iontana.
The Effect of Altered Streamflow on the l~ater Quality of
the Yellowstone River Basin, Montana.
'The Adequacy of Montana's Regulatory Framework for Water
Quality Control
Aquatic Invertebrates of the Yellowstone River Basin,
~-lantana.
The Effect of Altered Streamflow on Furbeari ng r~amma 1 s of
the Yellowstone River Dasin, Montana.
The Effect of Altered Streamflow on Migratory Birds of the
Yellowstone River Basin, Montana.
5
Report No. 8
Report ilo. 9
Report No. 10
Report No. 11
The Effect of Altered Streamflow on Fish of the
Ye 11 owstone and Tongue Rivers, t1ontana.
The Effect of Altered Streamflow on Existing Municipal
and Agricultural Users of the Yellowstone River Basin,
Montana.
The Effect of Altered Streamflo~1 on ~later-Based Recreation
in the Yello1·1Stone River Basin, Montana.
The Economics of Altered Streamflm~ in the Yellm·1stone
River Basin, Montana.
ACKNOWLEDGMENTS
This report was reviewed by and guidance received from John C. Orth,
Director of the Montana Department of Natural Resources and Conservation; Orrin
Ferris, Administrator of the DNRC's Water Resources Division; and Carole
Massman, of the DNRC's Special Staff.
Other DNRC personnel providing assistance were Peggy Todd and Pam Tennis,
who performed editing tasks, and Janet Cawlfield, Kris Macintyre, and Linda
Howell, typists. Graphics were coordinated and performed by Gary Wolf, with
the assistance of Gordon Taylor, Dan Nelson, and June Virag. The cover was
designed and executed by D. C. Howard.
Department of Fish and Game personnel who assisted with Part III of this
report were Larry Peterman and Chris Estes, who performed sampling, analysis,
and writing of the forage fish investigation. Much of the sampling for the
food habits investigation of Part III was performed by DFG summer field crews.
6
by
Allen A. Elser
Robert C. McFarland
7
r
PURPOSE
In the fall of 1974 a two-year study was initiated on the Tongue River to
assess fish populations present for these purposes:
1) To determine species composition and distribution,
2) To establish and evaluate diversity indices for various habitat
zones or sections,
3) To evaluate the potential impacts of water withdrawals.
STUDY AREA
The Tongue River's name originated from the Indian word "La-zee-ka,"
meaning tongue, for a tree-covered limestone slab outlined by barren rock which
resembled a buffalo tongue. The headwaters of the Tongue River rise on the
eastern slope of the Bighorn .Mountains of Wyoming and flow generally northeast
through Montana to join the Yellowstone River at Miles City. The length of
the Tongue River from the Montana-Hyomi ng border to its confluence with the
Yellowstone River is 326.5 km (202.9 mi).
The Tongue River's flow in Montana is controlled by the Tongue River Dam.
The dam, completed in 1940 for storage of irrigation water, impounds 84.9 hm3
(69,000 af) with a surface area of 1,416 ha (3,500 acres).
The Tongue River drains approximately 13,932 km2 (5,379 mi2), 70 percent
of which is in Montana, with an average annual discharge of 11.9 m3/sec
(420 cfs). The maximum recorded discharge was 377 m3/sec (13,300 cfs) on
June 15, 1962. The two typical stream bed formations found are: (1) in strong
current, gravel cobblestones and outcropping of bedrock, and (2) in slack or
slow current, silt and sand.
The average annual temperature for the basin varies from 4.4 to 11.1°C
(40-520F). Average annual precipitation varies from 22.9 to 40.6 em (9 to 16 in).
The basin of the Tongue River is underlain by the Fort Union Formation
of the early Tertiary (Eocene) Age which has a total thickness of about 610 m
(2,000 ft). Ninety percent of the soils were formed on sandstones and shales
laid down in the Cretaceous or Tertiary periods.
The river is an important source of water for irrigation, domestic use
by man and livestock, recreational use, and industrial use. ~lith the
increase in coal development in the Tongue River drainage, the river takes on
9
a new importance. The Decker-Birney Resource Study (U.S.D.I. 1974) conducted
by the Bureau of Land Management in April of 1974 identified strippable coal
reserves underlying 145,422 ha (359,333 acres) of the planning unit in the
Tongue River Basin. Approximately 115,000 ha (285,000 acres) of this planning
unit overlie superior reserves of 15 billion tons of coal economically
feasible to mine. Other coal reserves exist outside that study's planning
unit yet within the Tongue River·Basin.
Figure 2 is a map of the Tongue River in Montana; figure 3 shows its
longitudinal profile.
lQ
I
r
'
~
DECKER •
v
--
CITY
T8 Y
II
Ill
.IV
·"' ~~-
\~ ·;,
'Tongue Ri.., Oom ~
0 10 20 30 Miles ~~.t~.t~.t========1' ........ ~·
D~--'t0===2~0--~30 Kilometers
I
Tongu~ Ri11~r Rl66rlltJir \ l
______ ( ___ ~N_!A~ __ ,-------
WYOMING
Figure 2. Tongue River in Montana: major diversions, tributaries
and sampling sections.
11
10~0
1000
950
-900
5
c
.~ ;;
>
.!!
"' 850
800
7~0
700
175
300
-Hosford
""'--l[b Hosford Section
--Hanging Woman Creek
~ TIZ:b Birney Section
150 125 100
River Miles
270 240 210 180 150
Kilometers
'Figure 3. Long itud ina 1 profi 1 e of the
--Liscom Creek
~llb S-H Section
Section
75 50 25 0
120 90 60 30 0
Tongue R1 ver in Montana.
STUDY SECTION DELINEATION
Study sections were selected on the basis of the location of diversion
structures, access, fishing pressure, future and existing dam sites, and
the various habitats present. The Tongue River downstream from Tongue River
Dam was divided into five zones, identified by Roman numerals (figure 2).
Primary sampling sections (Ib, lib, Ilia, IVb, Vc) were established in
relation to irrigation diversion structures to evaluate fish distribution
(table 1). Another primary section, Vb, was established to obtain data for
a reach of river which would be inundated by the New Tongue River Reservoir.
These sampling sections were relatively short (2.5-4.1 km) and did not
adjoin one another. In all, sampling sites were established on 11 sections
of the river (see figure 2). Primary sections ranged in length from 2.5 to
4.1 km; gradients varied from 0.56 m/km (2,g4 ft/mi) near the mouth to 1.22
m/km (6.45 ft/mi) in the canyon.
TABLE 1. Description of major sampling sections, Tongue River.
Location Length Gradient
Section Upstream Barrier ( km)a {km) (m/km)
Ib T&Y Diversion 22.7 3.9 0.56
lib S-H Diversion 113.4 3.6 0.68
II I a Mobley's Diversion 145.8 4. 1 0.76
IVb Brewster's Diversion 252.1 3.6 0.65
Vc Tongue River Dam 300.2 2.5 1.22
a River kilometers above the mouth
Major habitat zones and sampling sites were delineated through the use
of aerial photos, USGS topographic maps, and ground measurements.
INSTREAM FLOW DETERMINATION
Instream flow levels were obtained through the use of the water surface
profile (WSP) program (USDI 1968) following procedures outlined by Dooley
(1975) and Spence {1975).
The validity of WSP and its potential use in determining instream flows
for a warm-water stream were investigated. Flows for migration, spawning,
and rearing were evaluated (Elser 1976). Predicted values for water surface
13
elevation and mean velocity were found to be not significantly different
from actual values. Although hydraulic characteristics predicted by WSP
are mean values, they are adequate for use with current knowledge of fish
requirements.
SAMPLING AND TAGGING
Six primary sampling stations were sampled six times in the fall of 1974.
Two sections (lib and Vb) were not sampled in the fall of 1975; the remaining
four sections were sampled three times each. Only section !Vb was sampled
in the fall of 1976 to check on the reproduction of the ·smallmouth bass
population. Four secondary sections (Ia, !Ia, IVa, and Va) were sampled in
the fall of 1974 for further definition of fish population distribution.
River fish populations were sampled by several methods. Electrofishing
gear with an output of 0-500 volts variable direct current, fished either
from a fiberglass boat as described by Vincent (1971) or from the banks of
smaller streams, was utilized to sample fish populations in the river and
tributaries. Baited trap nets (wire-frame, 3-ft hoop traps with l-inch mesh
webbing) were used for channel catfish. A 4-inch bar-mesh gill net was also
utilized·to sample fish.
Spring sampling concentrated on the migrant fish which utilize zone I,
the lower 32.8 km (20.4 mi) of the river, for spawning. A portion (10.9 km;
6.8 mi) of this section was sampled extensively by use of traps, gill nets,
and electrofishing techniques.
Each of three major tributaries to the Tongue River, Pumpkin, Otter,
and Hanging Woman creeks, was spot sampled at 16-to-24-km (10-to-15-mi)
intervals in 1974 to determine species composition and distribution.
SHOVELNOSE STURGEON
Shovelnose sturgeon (Scaphirhynchus platorynchus) were sampled by two
means: (1) by drifting the 4-inch bar-mesh gill net through an area free
of snags and (2) by electrofishing. The gill net was divided into ten 3m
segments to determine sturgeon distribution across the channel. The number
of fish captured in each segment was recorded for each drift. Samples were
taken at least three days each week of the run.
Several methods were used to tag sturgeon. In 1974, Floy anchor tags
were inserted immediately posterior to the dorsal fin. Observed tag losses
led to the use of No. 3 monel wing band tags placed over the anterior fin
rays of the pectoral fin as described by Schmulbach (1974). Irritation to the
pectoral fin caused by the monel tag resulted in the cessation of use of this
tagging method. Tagging in 1975 was accomplished by inserting the Floy
anchor tag in the pectoral girdle (Helms 1974), but tag loss associated with
this method was also high. A numbered aluminum strap tag encircling the
caudal peduncle at the base of the caudal fin as described by Christenson
(1975) was used in 1976. Several sturgeon thus tagged were held at the
Miles City National Fish Hatchery for observation. Severe irritation occurred
14
within two weeks. Floy cinch-up tags (FT-4) were also placed around the
caudal peduncle, assuming less ir~itation would occur. Test fish held at
the hatchery showed similar irritation to the extreme that the caudal fin
was lost. Finally, the Floy cinch-up tag was inserted through the flesh
immediately ventral to the dorsal fin and tightened. Observations on recap-
tured fish suggested good tag retention and little irritation.
SAUGER
Sauger (Stizostedion aanadense) samples were collected primarily by
electrofishing. The boat was adapted, however, to provide an efficient two-
man operation. The negative electrode remained on the bottom of the boat,
but the positives were supported by a boom system. One man dipped fish while
the other retained control of the boat. Sampling was conducted an average
of four days a week. Sauger were measured, weighed, and tagged, and a scale
sample was collected prior to release. The Floy anchor tag was inserted
immediately posterior to the dorsal fin. Drift samples were taken in an
attempt to collect sauger fry and eggs.
CHANNEL CATFISH
Channel catfish (Iatalurus punatatus) populations in the Tongue River
were monitored by sampling with baited traps constructed from reinforcing
bar material and chicken wire in three reaches of the river. Using rotten
cheese as bait produced the most fish per trap night. Catfish were tagged
with Floy anchor tags in 1974 and 1975, but high incidence of anchor tag
loss reported in other studies prompted a change to other tagging methods ...
A numbered plastic disc attached to the fish with 0.81-mm (0.032-in)
stainless steel wire immediately ventral to the dorsal fin was used in
1975 and 1976. Irritation associated with this tag resulted in the use of
the Floy cinch-up tag. Preliminary results suggest good retention and minor
irritation.
AGE AND GROIHH
Attempts to determine the age of shovelnose sturgeon by sectioning a pectoral
fin ray as described by Priegel and Wirth (1975) for lake sturgeon were
unsuccessful. The cross section was opaque and no annulus formation could be
detected. An attempt to determine growth by comparing weights and lengths
at marking and recapture was also unsuccessful, as is explained on page 47.
Age and growth of sauger were investigated by analysis of scales.
Pectoral spines taken from channel catfish were sectioned as described by
Marzolf (1955) and Sneed (1951) using an instrument similar to the one described
by Witt (1961). With this instrument, the spines were sectioned thin enough to
eliminate further grinding. The sections were coated with glycerin and aged
with the aid of a binocular microscope. The translucent rings were considered
to be year marks when they were distinct and continuous in all areas of the
section (Marzolf 1955).
15
POPULATION ESTIMATES
In order to assess the importance of the shovelnose sturgeon spawning
run into the Tongue River, it was necessary to determine the strength of that
run and variations in the number of fish using the river each year. The
validity of population estimates based on mark-and-recapture techniques is
based on certain assumptions:
1) marked fish do not lose their identifying marks and are recognizable
upon recapture;
2) either marked fish are randomly redistributed throughout the
population or the sampling effort is proportional to the density
of the population;
3) both marked and unmarked fish are susceptible to the same degree
of capture;
4) numbers of fish are not increased as a result of recruitment from
growth or immigration; and
5) losses from death or emigration are equal for both marked and
unmarked fish.
Since the sturgeon population is migrant, assumptions 4 and 5 are not
met, with continual immigration and emigration. However, Ricker (1958) felt
that the Schnabel estimator can still be useful even if not all conditions
are met completely.
The population of shovelnose sturgeon utilizing the lower Tongue River
was estimated using three formulas to compare and evaluate population strengths.
As found in Ricker (1975), the formulas are:
Schnabel N = L
t
Schumacher-Eschmeyer
Chapman or Modified Schnabel
~ where: N
Ct
Mt
Rt
=
=
=
=
population estimate
number of fish caught
number of fish marked
number of fish recaptured
N = L
t
All estimators are multiple censuses, involving the addition of
marked fish in the population. Negative bias enters into the estimates if
the combination of number of fish marked and number examined falls too low.
Ricker (1975) suggested that this bias can be ignored whenever the number
of recaptures is four or more.
16
1
,
The same methods were used to estimate the sauger population.
WATER TEMPERATURE
Water temperatures were monitored at stations la, lila, and Vc with
Taylor 30-day recording thermographs. The recording sheets were changed
monthly. All water temperatures were recorded in Fahrenheit degrees.
Daily maximum and minimum temperatures were tabulated and are given in
appendix B.
IMPACTS OF WATER WITHDRAWALS
Impacts were assessed by flow period. The year was divided into three
segments corresponding to the life-history phases of the important fish
species in the Tongue River: migration, spawning, and rearing (Stalnaker
and Arnette 1976). Since incubation periods of warm-water fishes are short,
incubation is ignored as a biological phase. It is generally agreed that
depth and velocity are the most important limiting factors during these
life history stages.
Depth is significant in maintaining suitable passage requirements
and in supplying the necessary wetted areas for spawning and food production.
In prairie stream ecosystems, Bovee (1975) suggested that if passage
(migration) requirements were met, spawning requirements would also be met.
Rearing, as a life stage, generally encompasses those times of the year
when fish are not engaged in migration or spawning. Therefore, rearing
flows are those which will maintain the habitat necessary for sustenance
of the fish species present.
The fall flow period encompasses the months of August (late summer)
through November. These flows coincide with late irrigation with late
irrigation withdrawals and are accompanied by warm water temperatures.
Temperature and water-quality requirements must be met during this time.
A reduction in flow during these months may elevate water temperatures
above tolerable limits and result in degraded water quality.
Winter (December, January, and February) is also a critical low-flow
period. Dewatering results in accelerated freeze-up of riffles and
depleted oxygen levels. It is during this time that fish population levels
are reduced. Fall and winter are considered rearing phases.
Spring (March through May) is the migration and spawning season for
most warm-water species. If adequate flows are maintained to ensure passage,
it is assumed that adequate water will be available for spawning.
The peak run-off period, May through July, is also important for
passage, spawning, and rearing. Additionally, spring peaks scour the
channel, cleansing the substrate interstices for food production and
successful reproduction.
17
FAUNAL ZONATION
Streams vary greatly in size, velocity, gradient, nature of the bed,
temperature, and other features. Generally, streams change from steep torrents
to sluggish meandering waterways as they proceed from source to mouth (Allen
lg69). Usually there are stages between the two extremes which are char-
acterized by specific environmental features and a particular assemblage of
fish species.
Many attempts have been made to associate particular fish faunas with
these defined zones. Huet (1959) devised a scheme for European streams using
four categories, naming each zone from the characteristic fish found in them.
In descending order of current velocity they are:
1) the trout zone
2) the grayling zone
3) the barbel zone
4) the bream zone
North American streams have been classified by Lagler et al. (1962) as
follows:
1) grayling
2) stream char
3) flowing water minnows and pike
4) bass
5) catfish, suckers, and quiet water minnows
Each of these zones is characterized by a particular set of combinations of
stream gradient and stream width. As the gradient diminishes, the headwater
fishes disappear and are replaced successively by others better adapted to the
changing environment. This was evident in the change of species diversity with
progression downstream in the Tongue River.
Fish population in the Tongue River exhibit a succession from torrent-zone
fishes (trout) to the quiet-zone fishes (catfish and suckers). While the upper
Tongue River in Montana cannot be considered a trout stream, the presence of
brown trout and other species associated with fast-water habitats suggests
zone 2 according to the classification given above.
RESIDENT FISH POPULATIONS
SPECIES OISTRIBUTION
Thirty-one species of fish representing 11 families were collected on the
Tongue River during 1974 and 1975. Of these species, four (burbot, paddlefish,
19
shovelnose sturgeon, and blue sucker) were taken only during the spring
sampling near the mouth and are considered to be migrant species.
Qualitative distribution of these species is shown in table 2. Grouping
by sections, though it obscures the variation encountered, illustrates
broad trends of the stream. Moutain whitefish and brown trout ·are confined
to the upstream zone.
TABLE 2. Distribution of fishes in the Tongue River by zones, 1974 and 1975.
Brown trout
Whitefish
Northern pike
Yell ow perch
Black crappie
Yellow bull head
Rainbow trout
Rock bass
Mountain sucker
Pumpkinseed
Sma 11 mouth bass
White crappie
River carpsucker
Carp
Stonecat
Shorthead redhorse
White sucker
Longnose sucker
Longnose dace
Black bull head
Green sunfish
Channel catfish
Sauger
Flathead chub
Goldeye
Burbot
Wall eye
Paddlefish
Shovelnose sturgeon
Blue sucker
Sturgeon chub
TOTAL No. Species
v
*
*
*
*
*
*
*
*
*
*
*
*
*
*
*
*
*
*
*
19
IV
*
*
*
*
*
*
*
*
*
*
*
*
*
*
*
*
*
*
*
*
*
*
22
III
*
*
*
*
*
*
*
*
*
*
*
*
*
*
14
II
*
*
*
*
*
*
*
*
*
*
*
*
*
*
*
15
I
*
*
*
*
*
*
*
*
*
*
*
*
*
*
*
*
*
*
*
*
20
NOTE: Common names of fishes used correspond to those presented by the
American Fisheries Society (1970). Corresponding scientific names are given
in appendix C.
20
Longitudinal distribution of fish in the Tongue River is influenced by
irrigation diversion structures. The T & Y Diversion is the upstream limit
for goldeye, walleye, burbot, paddlefish, shovelnose ·sturgeon, blue suckers,
and sturgeon chubs. Channel catfish did not occur above the Brewster Diversion.
Flathead Chubs are found upstream from.the Mobley Diversion, but in limited
numbers when compared to downstream sections.
Distributional patterns changed in 1975. Extensive high water during
the spring and summer resulted in damage to Mobley's and Brewster's diversions,
allowing fish passage. Five species (mountain sucker, yellow bullhead,
pumpkinseed, smallmouth bass, and black crappie) which had not previously been
found above Brewster's diversion were found in section Vc in 1975.
POPULATION NUMBERS AND SPECIES COMPOSITION
A comparison of the 1974 and 1975 electrofishing results is shown in
table 3. Fish captured per trip expressed as numbers/km were similar between
the two years. The number of species decreased in sections lb and lib
and increased in sections !Vb and Vc. In all cases, gains or losses were of
rare species. Section Vc showed the greatest change in both number of fish
(which increased from 231 to 292) and number of species (which increased
from 11 to 15). In the same section, sucker composition changed from short-
head redhorse dominance to longnose sucker dominance, and white suckers
showed a great increase.
Game fish concentrations were heaviest in section !Vb where they made
up 12.7 percent of the total number; the dominant game fish was smallmouth
bass, which ranged in length from 53 to 342 mm (2. 1 to 13.5 in). The pre-
ponderance of young-of-the-year fish indicates that smallmouth bass are
successfully reproducing. They were also found downstream from the S-H
Diversion, but the greatest concentration was near Birney.
Scales taken from smallmouth bass collected in section !Vb were used to
evaluate age-class strengths for 1974, 1975, and 1976. The distribution of
age classes 0 through IV is shown in table 4. Age 0 smallmouth bass contri-
buted 37.3, 7.3, and 73.3 percent of the total smallmouth sample in 1g74,
1975, and 1976, respectively. The low reproductive success of bass in 1975
is reflected in the number of age class I fish collected in 1976. High
discharges from the Tongue River Dam during the spring and summer of 1975 in
preparation for repairs to the dam apparently reduced smallmouth reproduction.
Reynolds (1965) suggested that water levels might be more important than
temperatures in initiating spawning of smallmouth bass in tributaries of the
Des Moines River, Iowa. In Courtois Creek, Missouri, smallmouth bass nesting
always began during a period of stable or gradually declining water levels
and was delayed or interrupted some years by floods (Pflieger 1975). Stable
flows during the spawning and incubation periods were considered more
important for successful smallmouth bass reproduction than a specific flow
level (White and Cochnauer 1975). This philosophy was strongly considered
when developing the minimum flow recommendations for the Tongue River dis-
cussed below under "Impacts of Water Withdrawals." ·
21
TABLE 3. Summary of electrofishing samples for the Tongue River, fall 1974
and 1975 (fish per kilometer)
Ib I lb !Vb Vc
Species 1974 1975 1974 1975 1974 1975 1974 1975
Gold eye 4 4
Rainbow trout 1 2 3
Brown trout 1 1
Northern pike 1 1
Carp 6 8 7 2 3 1 8 10
Flathead chub 14 8 16 9 1 1
Sturgeon chub 1 1
Longnose dace 2 -1 1 1 1
River carpsucker 3 3 14 3 5 2 30 20
Shorthead redhorse 9 9 22 36 29 37 80 37
Longnose sucker 1 2 5 9 6 10 16 77
White sucker 1 1 1 1 13 26 1 27
Mountain sucker 1 1 -1
Yellow bullhead -1 -1
Black bull head 1 1 4 3
Channel catfish 1 1 3 2 -1
Stonecat 1 3 4 14 6 6
Rock bass 1 1 3 7
Green sunfish 1 1 1
Pumpkinseed 1 -1 1 -1
Smallmouth bass 1 -1 2 9 6 -1
White crappie 1 -1 -1 1 1 1
Black crappie 1 1 1 1 -1
Yellow perch 1 1 1 1
Sauger 6 9 1 1 1 1
Walleye 1 1
Burbot 1
TOTAL 55 51 79 82 85 107 144 185
NO. SPECIES 18 13 15 13 19 20 10 15
NOTE: A hyphen (-) denotes a species present during one sampling period
and absent during the other; a blank indicates absence during both years.
22
l
TABLE 4. Summary'of age-class strength of smallmouth bass in the Tongue River,
1974-76.
PERCEtiTAGE OF TOTAL SAMPLE
Age Class 1974 1975 1976
0 37.3 7.3 73.3
I 37.3 65.5 8.4
II 12.0 16.4 13.3
I I I 10.7 9. 1 3.3
IV 2.7 1.7 1.7
Northern pike were also captured in section !Vb. The presence of small
northerns (236 mm or less in length) suggests that these fish are reproducing
in the river. The lower reaches of Hanging Woman Creek provide excellent
northern pike spawning habitat and probably act as a nursery for the
Tongue River population of northerns.
The Tongue River supports the only rock bass population in Montana .. The
greatest numbers of rock bass were found in sections IVb and Vb. All sizes
were represented in the samples.
The greatest number of channel catfish was found in section lib, with
the largest fish weighing 4.88 kg (10.75 lb). Sauger were most abundant near
the mouth, in section Ib, where they made up 13.1 percent of the total numbers
captured. The largest sauger caught weighed 2.2 kg (4.9 lb).
SPECIES DIVERSITY
Measures of species diversity are another tool for the quantitative and
qualitative description of a fishery. Investigations of longitudinal zonation
in stream fishes reveal that, in relatively unpolluted systems, diversity
increases downstream (Sheldon 1968), meaning the number of species increases
with proximity to the river's mouth, as in the Tongue. Factors which determine
the upstream limits of particular species also apparently contribute to the
regulation of species diversity. A study by Tramer and Rogers (1973) found
that variations in water quality upset the normal pattern of longitudinal
zonation of fishes. Where streams are undergoing stress from pollution,
species diversity may remain at levels similar to those in the headwaters
throughout the entire system. The disappearance of some of the headwaters
species is balanced by the appearance of others, and gains in the abundance
of one species are canceled out by losses in another. Therefore, from baseline
data, a change in water quality can be reflected by a change in species
diversity. It is a generally accepted concept that a large-scale environmental
23
stress exerted upon a diverse biological community results in a reduction in
species diversity (Cairns lg6g).
Species-diversity indices (d) have been used by biologists to provide
insight into the structure of natural communities and as indicators of
qualitative aspects of their environments. A low diversity index indicates
a largely monotypic community dominated by a few abundant species, and a high
diversity index suggests a heterogeneous community in which abundance is dis-
tributed more evenly among a number of species. Redundancy (R) (see Report
No. 5 in this series), also used as an index of the repetition of information
within a community, expresses the dominance of one or more species and is
inversely proportional to the abundance of the species (Wilhm and Dorris lg68).
While species-diversity indices have been used extensively with benthic
macroinvertebrates to evaluate degradational environmental conditions, they
have only recently been applied to fish populations (Sheldon 1g68, Jackson
and Harp 1973, and Harima and Mundy 1974). Shannon-Weaver diversity indices
were calculated for the fall 1975 sample and combined sample of fall 1974
and fall 1975 (figure 4). The fall 1974 sample diversities were also plotted
for comparison, but sections Ilia and Vb were omitted because they were not
sampled in 1975. With the inclusion of more data, the diversity indices
theoretically tend to the true population diversity, assuming no drastic change
over time. All fish under 152 mm (6 in) were excluded from the sample to
eliminate human sampling bias (the selection of the bigger fish when a choice
occurs in sampling). Figure 5 shows the linear regressions between diversity
indices (dependent variable) and the section (independent variable). Study
section diversity indices increased with proximity to the river's mouth.
In section Vc the index rise from 1974 to 1975 was attributed to a chan~e in
the number of fish/km (143 to 181) and a gain in the number of species (11 to
15). The probable reasons for these gains are two-fold: 1) prolonged high
releases from the reservoir in 1975 are not characteristic of past flows and
favor those species better adopted to fast-water habitats (mountain sucker
and smallmouth bass); 2) inspections and drawdowns of the dam may have
influenced the distribution patterns. The remaining sections had little
change.
Tongue River diversities are similar in magnitude to those calculated
for Rosebud Creek by Elser and Schreiber (1977). However, those on the
Tongue River tended to be higher, ranging from 1.8 to 2.9, as compared to a
range of 1.2 to 2.7 on Rosebud Creek.
SHOVELNOSE STURGEON
The shovelnose sturgeon (Seaphirhynchus pZatorynehus) is common in
portions of the Mississippi, Missouri, and Ohio river drainages. Its distri-
bution in the Missouri River has been limited by the construction of mainstem
reservoirs (Held 1969). In Montana, the shovelnose is abundant in the
mainstem of the Missouri below Great Falls and common in most of the larger
primary and some secondary tributaries of this river (Brown lg71). Shovel-
nose are abundant in the Yellowstone River downstream from the Cartersville
Diversion at Forsyth (Peterman and Haddix 1975). Anglers seek the
24
I
>. -·u;
~
Q) ,.
0
,.. -·u;
~ ., ,.
0
3
.·····~~································· .. ············· ·-;,;. ,.,.,. ...... . . :,...---,--.-:-~ --------.· __ ,...
2
1974 and 1975
----1975
........... 1974
0 ~--------r------------.------------~-------------,
1lc rilb llb lb
Section
Figure 4. Comparison of diversity indices for 1974 (6 runs) and
1975 (3 runs) and combined fall sampling (9 runs) at each primary
sampling station on the Tongue River.
3
2
1974 and 1975 (r = .9932)
----1975 (r=.9889)
······· ···· 1974 (r = .9480)
0 ~------~------------~----------~~----------~
1lc rilb llb
Section
Figure 5. Comparison of the Shannon-Weaver diversity indices for
1974 and 1975 fall fish sampling in the Tongue River and the combined
fall sampling at each of the primary sections excluding fish that were
less than 150 mm in length.
25
Ib
shovelnose, but pressure is considered light. The Yellowstone River shovelnose
offers an opportunity to evaluate the status of a relatively unfished popula-
tion in an unregulated river.
Sampling during the spring of 1974 in·the lower reaches of the Tongue·
River (downstream from the T&Y Diversion) produced a large number of
shovelnose sturgeon. Gonadal development revealed that the fish were in
spawning condition. Since previous sampling efforts in this reach of the
river failed to produce sturgeon, it appeared that the fish were migrating
into the Tongue to spawn.
In determining instream flow requirements for fish, if the life history
requirements for a sensitive species are met, then requirements for less-
sensitive species will also be met (Bovee lg74). The shovelnose sturgeon was
selected as a sensitive species because of its migrational patterns and
resulting passage and spawning flow needs. Passage flows are evaluated by
identifying shallow bars which could become barriers to the passage of adult
fish and determining the amount of water necessary to allow fish to pass
(Thompson 1972). The spawning run of shovelnose into the Tongue provides an
opportunity to investigate certain features of their life history and to
evaluate the instream flow necessary to maintain their run.
The objectives of this segment of the study were to: {1) sample the
shovelnose sturgeon spawning run into the lower Tongue River; {2) compare
population strength with flow and temperature; (3) collect life history data
on lengths, weights and sexes; {4) tag fish to aid in future studies to
evaluate migrational patterns, delineate home range, and determine fisherman
harvest.
FISH SIZE
Length Frequency
Fork lengths of sturgeon captured in the Tongue River in 1g75 and 1976
are shown in table 5. Half of the fish sampled in 1975 fell in the range
710-785 mm {28.0-30.9 in). The size interval 725-800 mm {28.5-31.5 in) contri-
buted 52.0 percent of the total sample in 1976. The average size and size
range of shovelnose sturgeon taken in the Tongue were larger in 1976 than in
1975 (figure 6).
26
r
.c u -0 u -0
20
15
~10
0 -c:: .,
u
~
If
5
500 600
I
' ' I ,
700 800
Fork Length (mm)
900
1976
1975
1000
Figure 6. Comparison of the 1975 and 1976 shovelnose
sturgeon fork length frequencies (by percentage of catch) in
the Tongue River.
In 1974, 427 shovelnose sturgeon captured in the Tongue River were
measured by Peterman and Haddix (1975). Since total lengths rather than fork
lengths were recorded in 1974, their results were converted by the regression
formula:
TL; 110.109 + 0.938 FL
where all measurements are in millimeters. The fork length range in 1974 was
449 mm (17.7 in) to 969 mm (38.1 in) with an average length of 700 mm
(27:6 in).
The length frequency of shovelnose sturgeon sampled downstream from the
Intake Diversion on the Yellowstone River in the spring of 1975 was plotted
and compared to the Tongue River sample for the same time period (Peterman
and Haddix 1~75). Yellowstone River sturgeon ranged from 287-815 mm (11.3-
32.1 in), with an average length of 508 mm (20.0 in). More than 50 percent
of the sample fell in the size class 330-480 mm (13;0-19.0 in) with the modal
interval of 386-404 mm (15.2-15.9 in). The length-frequency distribution of the
Tongue River sample is compared to the Intake sample in figure 7. Sturgeon
27
collected in the Tongue were considerably larger than those collected at
Intake. Additionally, the length distribution is much wider for the Intake
sample than the Tongue River sample, which was taken from a spawning
population and is not representative of the entire population; the Intake
sample was from the total population. The average length of shovelnose
migrating into the Powder River was 761 mm (30.0 in), comparable to those·
sampled in the Tongue River (Rehwinkel et al. 1976).
20
15
.s::;
I.) -0
(.) -0 ., 10
"' 0
c
Q)
I.)
~
Q)
D..
5
200
I
10
I
/
/
I
I
I
I
I
300
----Yellowstone River
---Tongue River
~
I I
I I
I I
I I I I .........
I I
I I l
I I II
I I I I
I I I I
I I I I
I I I I I I ~ -I I I I I I I I
I I I I I
I...-I I I I
\ I v I
\ I \ --.. 1', \1 \ I ' \
400 500 600 700 800 900
Fork Length (mm)
I I I I I I I I I I I I
20 30
Fork Length (inches)
Figure 7. Comparison of the fork length frequencies of shovel-
nose sturgeon taken in the Tongue River with those taken in the
Yellowstone River at Intake in the spring of 1975.
2!l
1000
I
40
,
Weight Frequency
Table 6 gives weights of sturgeon captured in 1975 and 1976. Of the
sturgeon examined in 1975, 23.7 percent exceeded 2.7 kg (6 lb}, 7.6 percent
exceeded 3. 6 kg ( 8 1 b}, and l. o percent exeeded 4. 5 kg ( 10 1 b}. In the
1976 sample, 21.6 percent exceeded 2.7 kg (6 lb}, 6.7 percent exceeded 3.6 kg
(8 lb}, and 1.8 percent exceeded 4.5 kg (10 lb}. The \~eights of the 1974 run
were similarly distributed (Peterman and Haddix 1975}. A sample of sturgeon
migrating into the Powder River averaged 2.42 kg (5.33 lb}, showing
close agreement with the Tongue River samples (Rehwinkel et al 1976}.
Figures 8 and 9 are weight-frequency histograms of sampling in 1975 and
lg76, respectively.
Shovelnose sturgeon captured in the Tongue River during the spring
migration were considerably larger than those reported elsewhere. In the
lower Missouri River, the average weight was 0.45 kg (1.0 lb}1 with
1.8 kg (4.0 lb} fish considered rare (Schmulback 1974}; Helms 1 1974}
found that the average weight of Mississippi River shovelnose was about
1.1 kg (2.5 lb}. Brown (1971} reported that 4.5 kg (10 lb} was
considered maximum shovelnose weight and that 3.2 kg (7.0 lb} was the
Montana record. While the Tongue River sample is of a spawning population,
the presence of considerably larger fish appears significant.
Length-Weight Relationship
The length-weight relationship was calculated for 874 shovelnose
sturgeon, utilizing the formula (Ricker 1975}:
w = ClX
where: w = weight in grams
= 1 ength in millimeters
C, x = constants
29
40 -
30 -
.&:;
u -0 u -0 ., 20 "' -
0 -c:
"' u
~ .,
c..
10 -
0
0
0
'----
I
I I I ' I
1000 2000 3000 4000 5000 6000
Weight (g)
2 4 6 8 10 12
Weight (pounds)
Figure 8. Weight-frequency histogram of the shovelnose
sturgeon collected in the spring of 1975 in the Tongue River.
30
I
7000
14 16
40 -
30 -
.<:::
<J -0 u -0
"' 20 -
"' 0 -c:
"' <J
~
"' Q.
10 -
I
I I I I I I I
0
0 1000 2000 3000 4000 5000 6000 7000 ,
Weight (g)
:' 0 2 4 6 8 10 12 14 16
Weight (pounds)
Figure 9. ~/eight-frequency histogram of the shovelnose
sturgeon collected in the spring of 1976 in the Tongue River.
31
The following equation, with a correlation of r = 0.8855 (figure 10), was
derived:
log w = 3.3439 log fl -6.2839
where: w = weight in grams
fl = fork 1 ength in mi 11 imeters
Zweiacker (1967) found a length-weight relationship for Missouri River
shovelnose sturgeon of:
log w = 2.79128 log fl + 0.68145
Helms (1974) reported the length-weight relationships of two pools (17 and 19)
on the Mississippi River to be, respectively:
log w = 3.526 log fl -2.2632
and
log w = 3.083 log fl -2.3136
All the above length-weight relationship equations have similar slopes;
the major difference between the Tongue River equation and the others is the
constant, which is indicative of the larger size of the population migrating
into the Tongue River to spawn.
A size difference was shown between males and females. t~ales were
smaller, averaging 738 mm (29.1 in) with a range of 523-864 mm (21.0-34.0 in)
in 1975 and 760 mm (29.9 in) with a range of 592-g34 mm (23.3-36.7 in)
in 1976. In 1975, females averaged 806 mm (31.7 in), ranging from 688 mm
to 937 mm (27.1 to 36.9 in); in 1976, they averaged 832 mm (32.8 in),
ranging from 5g2 mm to 934 mm (23.3-36.7 in). Weight differences were
more apparent, with males averaging 1.95 kg (4.30 lb) in 1975 and 2.17 kg
(4.78 lb) in 1976, while females averaged 3.20 kg (7.05 lb) and 3.62 kg
(7.97 lb), respectively.
Size at Maturity
Since sexual dimorphism is absent in shovelnose sturgeon, sex determination
was accomplished in two ways. Slight pressure exerted on the abdomen pro-
duced milt or eggs if the fish were nearing spawning condition. If repro-
ductive products were not produced, sex was distinguished by dist nsion of
the ovarian region and by the swelling of the ovipositor. If none of the
criteria were met, fish were recorded as undesignated sex. These methods
have been used to determine sex rations for other species (Snow 1963 and
Casselman 1974). Observed sex ratios for males, females, and undesignated
were 46.9, 12.9, and 40.2 percent, respectively, in 1975, and 63.6, 8.4, and
28.0 percent respectively, in 1976. The high incidence of undistinguishable
fish probably tends to mask the true sex ratio. Ho1~ever, it appears that
more males enter the run than females, a situation also true of paddlefish
(Elser 1976).
32
100,000
10,000
-.r:
"' ~
1000
100
r = .8885
1000
Length (mm)
Figure 10. The length-weight relationship equation of
all shovelnose sturgeon collected in the spring of 1976 in
the Tongue River.
33
10,000
The minimum lengths of ripe male and female shovelnose were 523 mm
(20.6 in) and 688 mm (27.1 in), respectively, in 1975 ·and 592 mm (23.3 in)
and 743 mm (29.3 in), respectively, in 1976. Other workers have also
reported male shovelnose sturgeon maturing at a smaller size than females
(Christenson 1975 and Helms 1974).
Theoretically, a fish should lose weight after spawning. A straight-line
relationship of weight at recapture versus weight at tagging would intersect
the equilibrium (no weight lost or gained) at the maturity size, providing
the fish were tagged prior to spawning and recaptured after spawning.
Weights from shovelnose tagged in 1975 (x) were plotted against weights at
recapture in 1976 (y) after spawning had occurred·. Since only males could
be positively identified both years, their weights were plotted (figure 11).
The intersection of the growth line and the equilibrium line was at 850 g.
Using the length-weight relationship of:
log w = 3.3439 log fl -6.2839
a fork length of 55g mm at maturity was derived for males. This corresponds
closely with the 561 mm reported for the Red Cedar and Chippewa river systems
of Wisconsin {Christenson 1975).
POPULATION ESTIMATE
. The estim~ted numbers of shovelnose sturgeon per kilometer of Tongue
R1ver sampled 1n 1975 and 1976 were similar using all three estimators
(table 7). Since confidence interval overlap was evident between estimates
of the ~am~ ~ear and beb1een different years, the differences do not appear
to be s1gn1f1cant. The Chapman estimator resulted in the lowest estimate,
but also had narrowest confidence intervals. The largest estimate resulted
from the Schumacher-Eschmeyer formula. While all requirements for a valid
pop~lation estimate were not met, the close agreement of the Tongue River
est1mates suggests a valid estimate.
TABLE 7. Estimated number of shovelnose sturgeon per km of the Tongue River,
1975 and 1976
lg75 1 g76
Estimator N/km 95% era N/km g5% era
Schnabel 409.4 327.3-546.6 482.8 405.8-596.8
Schumacher-417. 1 323.7-585.9 537.2 449.7-667.0
Eschmeyer
Chapman 402.8 388.0-418.8 478.6 402.3-590.5
a CI = confidence interval
34
TIME OF SPAWNING
In 1975, the first sturgeon was collected on May 9, with large concen-
trations appearing around t1ay 21 (figure 12). The last sturgeon was
collected on August 7, although sampling continued until August 10. The
first ripe male (one from which milt could be stripped) was taken on June 3;
no ripe females were caught in 1975. Internal examination of two sturgeon
on July 10 revealed a few black eggs remaining in the body cavity. It was
assumed that these fish had spawned in the Tongue River.
"' ..
~
:::0 -Q.
0
c.> .. a: -0 -.1:
.!!' ..
3::
7000
6000
5000
4000
3000
2000
1000
0~~----~----,-----~------~-----r----~~--~
0 1000 2000 3000 4000
Weight at Togging
5000
(g)
6000
Figure 11. Linear regression analysis of the weight at
tagging (before spawning) compared with the weight at recapture
(after spawning) of shovelnose sturgeon in the Tongue River.
35
7000
~ u .,
"' ., ......
E -.,
w "' en ~
0 ..c:
u ..
0
180
150
120
90
60
30
~ a: E a: <.?
(f) .. .., a: <.?
a: "' " <.? (f) (f)
" " 0 a: (f) z " c.o-.,-(/)~ Ci. .. c.o (f) _o
ocn-E 0 E E ~ E .. 0 E " E 0 .!!! ..
0 ... ~ .,_
E ... -;;i: I -o-~ .,Ec ;:: (f) " ... z ....... ... .. -"~ (f) .--Q. -~ ..... =a_;: ~ ~ ~.!!
;; ;; c ;; e ... .. ~ -...
0 " ~ .: a..: ~ " " ~ 0 ;;: -~-.!!o
.c
.!!!
~ .., ..,
0 ...
~ -
.·
(f)
z
(f) ..
0
E .c
~ $'. -.. ;:: ..,
" .., ... 0 ~ ... -~
" ~
.!! -
. · ·· ..
(f) z
(f)
~
0
E
$'.
c
" ... ..
• .!!
'• ' ' I \
' ' ' '
..
.: (/) -z
""' " 0 ~
(f) 0
z E
"'-" ;; "' ... .!! ~
I \ ,,
/ \ ,' ' .... ' .. ' ' \ ' ' ... ... ':'.... ,' ' ............. ,' ,, ...... .. .....
I -----Temperature
····· ····· Discharge ~ I
I \ I
'
.. ········· ••• . ·.
· ..... .
I ' •· l · ,.. ......
\ • • \ '' ' I I ' ,, ' ' .. --.. :,' I \ I \ I ',,.,
I \ I \ I
I \ ,' \ t
I \. :t \ ,'
I \! ·I \ I
I \"I '' ' :, , •/ .···. ' : \ ,: ,.. ··.·
I \ I · .. , . • • •
I \ I
I \
I .•
' I ',• ··········· ....
·.
·.
... ... ········ ...
0~---~---~---~-,---~----r---,----~---~---~---~-,---~----r----r---,----~---+
10 20
MARCH
10 20
APRIL
10 20
MAY
1975
10 20
JUNE
10 20
JULY
10 20
AUGUST
Figure 12. 'Five-day average temperatures (DC) and discharges in relation to the spawning
activities of the shovelnose sturgeon and sauger in the spring of 1975 in the Tongue River.
35
30
.,
~
:::> -0
~
20 ~
E
{!!.
10
5
The first shovelnose was collected on April 22 in 1976; large concen-
trations appeared on May 7 (figure 13). Sampling continued until July 27,
but the last sturgeon was taken July 15. The first ripe male was collected
on June 2 and the first ripe female on June 7. The last spent female was
caught on June 29, but other females were taken after this date that had
neither spawned nor were ready to spawn.
Spawning occurs in the Tongue River from early June until mid-July.
In the Red Cedar River, Wisconsin, Christenson (1975) reported that shovel-
nose sturgeon spawned from the last week of May through the first week of
June. Mississippi River sturgeon spawned from May 30 through June 14
(Helms 1974). Rehwinkel et al. (1976) reported the first 1976 sturgeon in
the Powder River was taken on April 13 with the farthest upstream migrant
taken on May 13. No ripe sturgeon were collected on the Powder River.
HABITAT PREFERENCE
Depth
The gill net used in sampling was marked off in three-meter intervals;
the number of fish taken in each segment was recorded. One end of the net
was always kept close to the shore. In a selected reach with a uniform
bed, 85 shovelnose were taken throughout the season. The catch rate per
net section was plotted against the bed profile (obtained from WSP) to
determine depth preference (figure 14}. The majority (61.2 percent) of the
fish were taken from the more gently sloping edge of the stream 15 to 21 m
(49to 69ft) from the shore. The mode of the sturgeon catch occurred at
the thalweg. Depth preferred by the fish ranged from 0.43 m (1.4 ft) to
o.go m (3.0 ft}, with an average of 0.67 ±0.17 m (2.2 ±0.6 ft). These
depths correspond to those found by Bovee (1976) for snovelnose sturgeon.
Discharge
Daily sturgeon catches were totaled for each week of the sampling season.
To evaluate the catch rates in relation to discharge, two catch-per-effort
rates were calculated.
1} The total catch for each week was divided by the length of river
sampled during that week, resulting in the number of fish taken
per km.
2) The week's catch was divided by the total number of sampling efforts
made that week, producing the number of fish caught per trip.
Both catch rates were averaged over the ·week to avoid sectional bias,
since one to three sections were sampled during any week. Optimum flow con-
ditions were evaluated in terms of the catch rates; as Zakharyan (1972)
showed, the scale of spawning depends on the number of fish taking part:
37
90
75
60
u .,
"' .., .....
E
w ., 45 CXl 0>
~
0
~ u
"' 0
30
15
0
...
" en oen
z enZ
a: en zen
"' -:;; .!! en., en
en --z ~ .!:a: 0 ~ en o.!! 0 en D .. en -"' DZ E E ;; " z OU>.!!. " 0 D 0 en ..,en 0 E~ -... E u " E., u
0 " OD ;: --E " a: .. en D a:;; .. 0 .<: " " 0 D .!! G D .. "' 0. z e>E .~E 0. O.o. " en en E .. Q.C
~ en_ ~ ~ .. D D -;:~ --:;; " -ii-~ .. .. -.. ..... .. ..... -• E
~ ~ ~ "'o. .!: <=.!: 0 -~ ~ 0 ;:: -;: ;;: _!!., o-0.--.!! D
I I I I
, ....... -
I ............ ..
I ~~
I ................ ,'',
I "',.., '
-----Temperature
......... Discharge
" , I , I , I I
,,--, ,'
I \ I
: \ I
I . \ I
I .'\' • • I I , \ , ~ I
I •\''•,(\1
I \ I '" I
I \ I \~
, ...... ~ \ I
I ~I
I , ........ 4,
I
I
I
I
I
I
,, I •.•
', ·'... 0 ••• 0 •••
..... I I I ..
..
10 20
MARCH
, , ,
I '..• ,
I
I
0 ·I 0 0 0 0 0 0 0
I ,
10 20
APRIL
\i'
10 20
MAY
1976
10 20
JUNE
0 ••
10 20
JULY
'• .... . .. .....
0 ° '
10 20
AUGUST
Figure 13. Five-day average temperatures (°C) and discharges in relation to the spawning
activities of the shovelnose sturgeon and sauger in'the spring of 1976 in the Tongue River.
35
30
25 u
0 -.,
~
:II -0
~
20
.,
a.
E
{!
~
Cll -0
15 3:
10
5
--
25
Water Surface
0
' I
' I
' I 20 ' Bottom Profile ' I
' I ' ' I .3 ' I ' .r. ' I u ' I -15 0 ' (.) ' I -' I 0 ' Catch Rate E ., ' I .6
"' ' J .r.
0 ' I Q.
c: I "' "' 10 ' 0 u ' I w ~
0.0 "' ' I a.. ' I ' ' I .9
' I
' I ' 5 ' I
' I
' I
' I ' 1.2 ' '--------1
0
0 6 36 39 42
Distance
Figure 14. Comparison of the catch rates of shovelnose sturgeon with the bottom profile
of the river channel for one reach of the Tongue River.
A quadratic regression was run with catch rates plotted against the
average weekly discharge using the model:
Y = a0+a 1x + a 2x2
where a0 , a 1 , and a2 are constants
This regression produces a hyperbola.
The graphs for the 1975 sturgeon run.depicted in figure 15, show that
the optimum discharge for shovelnose sturgeon was between 65 m3/sec (2300 cfs)
and 68m3/sec (2400 cfs). Plotting discharge freguency for 1975 reveals that
the most sturgeon were taken in the interval 34 m3/sec (1200 cfs) to 45 m3/sec
(1600 cfs). The two discharge figures differ because the optimum is based on
catch rates at predicted flows from the regression model and the second
interval on the total number of fish caught at each flow. Sampling bias
produced by varying section lengths resulted in the difference between the
two discharge figures.
In 1 g75, the optimum discharge~ for the 1 i near and trip catch rates were
30.90 m3/sec (1090 cfs) and 34.91 m3/sec (1233 cfs), respectively (figure 16).
The majority (56.5 percent) of the sturgeon in the discharge frequency
histogram were taken at discharges between 11.3 m3/sec (400 cfs) and 22.7
m3Jsec (800 cfs). Runoff patterns for the years 1975 and 1976 differed,
with 1975 considered a high water year. No sturgeon were taken either year
when flows fell below 8.50 m3/sec (300 cfs). Sampling efficiency decreased
noticeably when flows exceeded 62.29 m3Jsec (2200 cfs) because the sampling
equipment was more difficult to operate in higher flows.
Based on the quadratic regressions, it appears that a minimum flow of
8.50 m3;sec (300 cfs) is necessary to provide shovelnose sturgeon passage.
The upper limit was not estimated due to the decreased sampling efficiency
at greater flows. The quadratic regression was utilized because, for any
environmental condition, there is typically an intermediate range, with
less favorable conditions above and below (Ricker 1975). For example,
there may theoretically be flows too low or too high for successful migration;
the optimum is intermediate.
Temperature
The linear and trip catch rates (dependent variables) of sturgeon were
compared with the five-day average minimum and maximum water temperatures
(independent variables) using the quadratic regression model described
above. The graphs for the 1975 shovelnose run (figure 17) show an optimum
mini~m temperature of 18.30( (650F) for the linear catch rate and 16.9oc
(62.5 F) for the trip catch rate. The optimum maximum temperatures for the
linear and trip catch rates were 2o.ooc (680F) and 18.30C (60.50F),
respectively. In 1976 the minimum linear and trip catch rate averages
40
,
12
II
"! 10
-;; .. 9 .. • ' E 8
~
' .c
n 7
~ 6
" a:
5 .c u ;;
u 4
3
2
0
20
~ ..
" • ' E 15
~
' .c
~
~ 10
" a:
' .c
!! 5 " u
0
Linear Catch Rote Trip Catch Rote
vs. Oischarc;~e vs. Discharge
25
~ .. _,
' .. I • I ' ' Q. I \
\ ~ I ' 20 \ .c I ,-, ~ \ , ' I / ' \ I \ .. I I I ' 15
" I I ' a: I
I ' I I
' .c I I I !!
I ' " 10 I I I u
I I I I
I I I I
I I I
I I 5 I I
I I I I I I I I I I I I
0
0 20 40 60 80 100 120 140 0 20 40 60 80 100 120 140
Discharge (m 3/sec) Discharge (m 3/sec)
Figure 15. Quadratic regression analysis of discharge versus
catch rates of shovelnose sturgeon in the Tongue River in the spring of 1975.
Linear Catch Rote Trip Calch Rate
vs. OischarQe 40 vs. OischorQe
-;; .. .. • ' ,-, -~ 30 ,,
~ , ' / ' , ' .c / ' I \ ~ / ' I \ I ' \ 20 \ I \ .. I \ I " I ' ' a: I \ .c I I I \ u 10 I I I ;; I \ u I I \ I
I I I ' 0
0 10 20 30 40 50 60 0 20 40 60 80
Discharc;~e (m 3!sec) Discharge (m 3/sec)
Figure 16. Quadratic regression analysis of discharge versus
catch rates of shovelnose sturgeon in the Tongue River in the
spring of 1976.
41
were l7.9°C (64.~°F) and l7.7°C (63.9°F), respectively (figure 18). Maximum
temperatures were 21.2oc (70.20F) and 21.5°C (71.70F), respectively.
Therefore, the optimum temperature range for spawning of shovelnose
sturgeon is between l6.goc (62.50f) and 21.5°C (70.7°F). The majority of
the sturgeon were captured at temperatures from l8.9°C (66°F) to 25.60C
(78°F). Brown (1971) stated that shovelnose sturgeon spawn in Montana at
temperatures between l5.6oc (6QOf) and 21.7°C (70 F). This corresponds
closely with the temperatures found in the Tongue River. In the Powder
River the peak of the shovelnose sturgeon run occurred at l6°C (60.8°F);
however, these fish were not considered ripe (Rehwinkel et al, 1976).
Christenson (1975) found sturgeon spawning occurred in the Red Cedar River
of Wisc?nsin at temperatures between 19.4-Zl.lOC (67-700F).
SAMPLING AND TAGGING STUDIES
Egg and Fry Sampling
Egg and fry samples were taken at least once each week during the
shovelnose sturgeon run in 1975 and 1976 by holding a fine mesh drift sampler
in the current for 30 seconds. Three riffle areas were sampled and a drift
taken at 10m intervals across each riffle. Material collected in the net
was sorted and washed at the time of collection. Samples were then preserved
in 10 percent formalin and hand picked with the aid of a microscope. A few
eggs and small fish were taken, but none were positively identified as
shovelnose sturgeon.
Several attempts were made to artifically propagate shovelnose sturgeon.
In one attempt, eggs were stripped from a ripe female, fertilized by one
male, and incubated in a jar, agitated by air circulating through the eggs.
Second, several sturgeon were held at the Miles City National Fish
Hatchery until they were considered gravid. Eggs were stripped into a pan
and milt added. Half of the eggs remained stationary and the otherhalf were
stirred for 30 minutes, allowing the eggs to water harden. Both batches were
then placed in hatching jars and kept moving to provide oxygenation. Eggs
were cleared with glacial acetic acid to check on development. Because no
development was apparent in either attempt, it was assumed that the eggs were
not successfully fertilized.
Tagging Studies
Weight Losses. In 1975, 28 fish that had been tagged in 1g74 with
monel tags were recaptured. The monel tag returns demonstrated a significant
weight loss of 0.36 kg (0.79 lb) per fish (p < .001). Eight sturgeon
(4.5 percent) tagged with anchor tags in 1974-and recaptured in 1g75 showed
a weight gain of 0.36 kg (0.79 lb) per fish (p = 0.015). In the 1g75 samplin~,
7.9 percent (14 of 178) of the anchor-tagged fish and 12.8 percent (31 of 243)
of the monel-tagged fish were returned from 1974. (Only 28 monel-tagged fish
were recaptured; three of them were recaptured twice, producing a total of
31 recaptures.) Total returns in 1975 were 10.7 percent (45 of 421) of those
fish tagged in 1974.
42
,
:;;-
0 a • ' E
~
' "' D -
a a
"'
"' " " ...,
~ .. .. • ' E
~
' "' D
~
" "'
"' " " ...,
12
II
10
9
8
7
6
5
4
3
2
Linear Catch Rote
vs. Temperature
.v-20.0°C
18.3 °C ...,.. ·:.: -~
? ' · .. ,. ' . /.". ' ... ,... ' ·.
1:" \ .
ll \ :
I: \ · ..
I_:" \ '.
I: \ ·.
I! \ \
li I \
I i I · ..
li I .
~ I
-25 ~ a a
{ ...
:E 20
' "' D -
.. 15 a
0:
"' " ~ 10
5
Trip Catch Rate
vs. Temperature
16.9 oc ~ 18.3 oc I-~~
I / I "-.
I .: \ · ..
I .: I · ..
I : I '.
I :' I · ..
I : I '
I :" I \
I : I
I :" I
I : I
I i I
I : I . I
~ I
t I
t I
t I
Minimum
Maximum
~ I
0 -r--~1~=~---r----.---~--~-I I
' 0
5
20
15
10
5
0
5
10 15 20 25 5 10 15 20
Temperatura (°C) Temperature (°C)
Figure 17. Quadratic regression analysis of minimum and
maximum water temperatures versus catch rates of shovelnose
sturgeon in the Tongue River in the spring of 1975.·
Linear Catch Rote
vs. Temperature ~ 40
Trip Catch Rote
vs. Temperature
25
Minimum
Maaimum
17.9oc ~' .···<21.2°C
/ " ·.
..
a
{ 17.7 oc / 21.5"C ~,lr...-·· ...
I . \ · ..
I \
I _:" 1
I I
I \
I I
I \
I I
I I
I
10 15 20
Temperature (°C)
25
...
·~
'30
"' • -
~ 20 " 0:
"' !:?
~ 10
0
/ . ' ·. I : .
I . \
I : I
I \
I
I I
I I
I I
I I
I I
I I I
I 1
I I
5 10 15 20
Temperature (°C)
Figure 18. Quadratic regression analysis of minimum and
maximum water temperatures versus catch rates of shovelnose
sturgeon in the Tongue River in the spring of 1976.
43
25
Twenty-one fish (8.6 percent of the total sample) that had been tagged
in 1974 with monels were recaptured in 1976. A weight loss of 0.62 kg (1.37 lb)
per fish (p = 0. 19) was demonstrated. Monel tags were not used in 1975;
however, by considering the weight at recapture in 1975 as the tagging weight,
weight loss or gain from 1975 to 1976 could be determined. Thus, monel-
tagged fish lost an average of 0.10 kg (0,22 lb) per fish (p = 0.05) from
1975 to 1976. Twenty-two sturgeon (3.1 percent of total) tagged with the
anchor tag in 1975 and recaptured in 1976 displayed a significant weight
gain of 0.06 kg (0.13 lb) per fish (p = 0.01 ). Total returns in 1976 were
9.4 percent (67 of 709) of those tagged in 1975. The 1975 and 1976 rates of
return are comparable.
The regression plot of weight at recapture versus weight at tagging
reveals the significance of the weight loss or gain associated with the two
tagging methods (figure lg). All regression lines for anchor-tagged fish
fell above the equilibrium line (that line showing no weight gain nor loss),
indicating that fish gained weight over the period shown. Monel-tagged
sturgeon fell below the equilibrium line, suggesting weight loss over the
time period. It is apparent that the monel tag caused a physiological stress
in the sturgeon which resulted in a significant weight loss.
Movement. Of the 94 shovelnose sturgeon tagged and recaptured in 1976,
the majority were recaptured in the same section in which they had been tagged.
Time between tagging and recapture ranged from 1 to 60 days. The sampling
period was stratified into monthly segments to detect differences in movement
with time. As shown in table 8, upstream movement was greater than downstream
movement in May and June. The differences were not considered significant
because of the small sample size. In July, upstream and downstream movements
were nearly equal.
In 1975, 90 percent ( 45 of 50) of the sturgeon tagged and recaptured
that year showed no detectable movement. Six percent (3 of 50) showed
upstream movement, while 4 percent moved downstream.
Comparisons were made between tagging locations and recapture location
for fish recaptured in subsequent years. A fish was considered to be in a
different location if there was a difference greater than 1.6 km (1 mi). No
sturgeon tagged in 1974 and recaptured in 1975 was recaptured downstream from
where it was tagged (table 9), and of those fish tagged in 1974 and recaptured
in 1976, the majority (89.2 percent) were recaptured either upstream or in
similar locations to where they were tagged. From 1975 to 1g76, the sturgeon
exhibited a strong tendency to return to the same place (75.0 percent).
Angler Returns. The shovelnose sturgeon provides an excellent spring
fishery for those anglers who pursue them. Returns of tagged sturgeon by
fishermen show a light harvest (table 10). Returns of 1974-tagged fish
totaled 1.67 percent by 1975; 1975-tagged fish were returned at a rate of
1.41 percent (0.71 percent/year). Overall returns totaled 1.11 percent,
indicating a lightly-utilized resource. An exploitation rate of 5.0 percent
was considered an acceptable level for lake sturgeon on the Menominee River
in Wisconsin (Priegel 1973). The lake sturgeon is a slow-growing, late-
maturing fish which does not survive high levels of exploitation. The
current exploitation rate for shovelnose sturgeon on the Tongue River is not
excessive.
44
.,
~
Anchor Tags
I • • • • • 1974 mork, 1975 recapture
Y'l.1485•-176.9397
r'.9888
2----1974 mark, 1976 recapture
y, 1.3023• -401.7037
r' .9277
3 --1975 mark, 1976 recapture
y,_9899• + 79.4105
r'.9833
7000
6000
5000
Monel Togs
4• • • • • 1974 mark, 1975 recapture
y,_6146• + 466.4699
r'.8228
5----1974 mark, 1976 recapture
y,_5605• + 608.8107
r' .9802
6--1975 mark, 1976 recapture
y,_8267•-61.5117
r'.8311 ,2
I
I .I
/
I
/ .
I ,•'
I .··
I •·
/ .·.
I .
/ .·
I .··
I . • ..
. . . .
3
6
.4
= 4000 Q. I .·
/ .·
• ................ 5 .. · .......... .· / 0
<.> .,
a: -• I .· / ..
.· / .· / .· / . / .·..-
0 3000 I .· •'/ .. _, .·..--""' "' .,
3:
2000
1000
0
/
/
I.
.~ .·...-.......
,•/ v
/-•----Equilibrium
1000 2000 3000 4000 5000
Wei~ht at Togging (g)
6000
Figure 19. Comparison of the linear regression analysis of
the weight at tagging versus the weight at recapture of monel-
and anchor-tagged sturgeon over the three years of sampling
in the Tongue River.
45
"
7000
TABLE B. Percentage and direction of shovelnose sturgeon movement for May,
June, and July 1976 in the lower Tongue River
Month of Upstream Movement Downstream Movement
Recapture Sample No
1976 Size 1.6-6.4 km 6.4 km 1.6-6.4 km over 6.4 km Movement
May 19 36.8 0.0 10.5 0.0 52.7
June 65 16.9 3 0 1 10.8 1.5 67.7
July 10 16.7 8.3 16.7 8.3 50.0
TABLE 9. Difference between place of tagging and recapture for shovelnose
sturgeon in the lower Tongue River, 1974-76, expressed as percentage.
Year Percentage Recaptured
Sample
Tagged Recaptured Size Downstream Same Upstream
1974 1975 37 0.0 43.2 56.8
1974 1976 37 lO.B 37.8 51 .4
1975 1976 88 20.5 75.0 4.5
TABLE 10. Summary of tagged shovelnose sturgeon from the Tongue River
returned by anglers, 1974-1976.
Year Returned
Year Tagged Number 1974 1975 1976 Total
1974 420
1975 709
1976 761
TOTAL 1890
One angler who kept a log
(6.6 percent) had been tagged.
were fema 1 es.
3 4 0 7 (1.67%)
9 1 10 (1.41%)
4 4 (0.53%)
21 (1.11%)
in 1975 caught 152 shovelnose, of which 10
Of the 80 kept and dressed, about 90 percent
46
Growth. During the 1975 and 1g75 spawning runs, 151 sturgeon were recap-
tured after having been at large 12 to 24 months. Empirical ·growth rates were
divided into years and types of tags to assess differential growth rates as
related to type of tagging. Sturgeon tagged with anchor tags lost an average
of 1.5 mm (0.06 in) from 1974 to 1975 and gained an average of 2.2 mm (0.2 in)
from 1975 to 1976 and 1.4 mm (0.06 in) in length from 1974 to 1976. Only the
gain from 1975 to 1976 was significant (p < .02).
Shovelnose sturgeon tagged with monel tags showed significant length loss
for each year. Fish tagged in 1974 and recaptured in 1975 lost an average
7.0 mm (0.3 in) while those tagged in 1975 and recaptured in 1976 lost an
average of 5.2 mm (0.2 in). Average loss from 1974 to 1976 was 8.0 mm (0.3 in).
All losses were significant (p < .01). Apparently the monel tag resulted in
physiological change drastic enough to alter the growth rate of the sturgeon.
No conclusions could be made concerning the growth of shovelnose sturgeon
based on individually marked fish because of the weight loss associated with
the use of monel tags.
SAUGER
Sauger (Stizostedion oanadense) and walleye (Stizostedion vitreum) are
important to the sport fishery of the lower Yellowstone River. Native to
Montana, the sauger inhabits the Missouri River drainage below Great Falls
and the Yellowstone drainage below Billings. It was first recorded in
Montana by the Lewis and Clark Expedition (1804-1806). Preferred habitat
for sauger includes turbid rivers and shallow portions of lakes and reservoirs.
Sauger generally spawn in gravelly or rocky areas in the spring when tempera-
tures reach 4.4-lo.ooc (40-5QOF). Fish migrate upstream to spawn, often
moving into tributary streams.
A sauger spawning run occurs in the Tongue River, with fish moving out
of the Yellowston~ in the spring. This migratory population offers an
excellent opportunity for anglers to pursue the sauger. Sampling in the
spring of 1g74 indicated that large numbers of fish enter this run. Early
high water, coupled with above-normal sedimentation, prevented good sampling
in 1975. · However, in 1976, a mild spring provided good sampling conditions,
and a large sample was collected.
FISH SIZE
Length-Weight Relationship
In 1976, 1004 sauger were taken in the lower Tongue River. Lengths and
weights were recorded for 1001 of these. The average length and weight of
the total sample was 379 mm (14.9 in) and 441 g (0.97 lb), respectively. Sexes
were differentiated by the presence of milt for males and/or a distended
abdomen and protruding ovipositor for females. Ripe males were common in
the sample, but no ripe females were taken. Males dominated the sample,
contributing 85.7 percent, while females added 3.2 percent. The remaining
11 . 1 percent were of undetermined sex. Fema 1 es were 1 a_rger than rna 1 es,
47
averaging 454 mm (17.9 in) in length and weighing 1044 g (2.30 lb) while
males averaged 374 mm (14.7 in) and 409 g (0.9 lb). Sauger taken in gill
nets from five sampling areas of the lower Yellowstone River exhibited
similar length and weight distributions (Peterman and Haddix 1975).
The weight-frequency distribution of the 1976 sauger sample is shown
in figure 20. The peak of the sample occurred at 300 g (0.66'lb), with the
greatest abundance falling in the size class 200-350 g (~.44-0.77 lb).
Sauger length-frequency distribution for 1976 is shown in figure 21.
Lengths ranged from 250 mm (9.8 in) to 545 mm (21.5 in) with the peak occurring
at 375 mm (14.8 in). Three age classes were evident, and scale samples showed
these ages to be IV (320 mm total length), V (375 mm total length), and VI
( 430 mm tota 1 1 ength).
Using the 1001 lengths and weights and computing a linear regression on
the Log 1 g of the weight (dependent variable) and LoglO of the length
(indepen ent variable), the resulting.equation is:
Log w = 3.3438 log tl -6.016
with a correlation of r = 0.9577 (figure 22). The length-weight equation for
1.501 sauger from Lake Winnebago, Wisconsin (Priegel 1969) was:
Log w = 3.1309 log 1 -2.5091
Age and Growth
Scales from 274 sauger taken during the spring of 1976 were analyzed for
age and growth. Ages ranged from three to nine years, ~lith age group IV the
dominant age (32.5 percent). Age groups IV, V, and VI made up 73.4 percent
of the total sample (table 11). Growth rates for the sauger collected in
the Tongue River are slower than those observed in other northern waters
(table 12). The Tongue River sauger were collected in the spring; growth rates
in other rivers may have allowed more of the season for additional growth.
TABLE 11. Age and mean length of sauger taken in the Tongue River, spring of
1976
Age Number of Fish Mean Length (mm) Range (mm)
III 26 289 259-312
IV 89 332 277-385 v 62 374 332-404
VI 50 418 387-443
VII 31 444 419-475
VII I 12 478 453-565
IX 4 544 504-573
48
"" ..
~
:I -Cl. c u
.<:
"' ii: -c
120
100
80
60
~ 40 .,
.0
E
" z 20
0
12
10
.<: <> -8 c u -0
., 6
"' c -c: .,
<> 4 ~ .,
a..
2
0
100
240
200 300 400 500 600 700 800 900 1000
Weight (g)
Figure 20. Weight-frequency graph of sauger collected in
the spring spawning migration of 1976 in the Tongue River.
., s
: I
280 320
Figure 21.
sauger taken in
Tongue River.
el
I
360
PI
I
l:;f
I
400
Length (mm)
~
I
440
~
I
480 520
Comparison of the age and length frequency of
the spring spawning migrations of 1976 in the
49
~
I
1100
560
10,000
1000
100
100
r = .9577
1000
Length (mm)
10,000
Figure 22. Length-weight relationship equation of all sauger
collected in the spring of 1976 in the Tongue River.
50
,
,
TABLE 12. Comparison of calculated growth of Tongue River sauger with those
from other northern waters (mm).
Age
Water Sample I I I III IV v VI VII VI II IX
Tongue River 274 289 332 374 418 444 478 544
Ye 11 owstone R. a 413 211 257 310 356 394 4B5 574
L. Winnl\>ago,
Wise. 784 124 241 307 335 356 376 3B9 401
Upper Mississippi
R. b 42 124 228 302 345
Lewis & C~rk L.
S. Oak. 479 160 312 414 482 321 438
a Haddix and Estes 1976.
b Summarized in Priegel 1969.
POPULATION ESTIMATES
The number of sauger moving into the lower Tongue River in 1976 was
estimated using the Schnabel, Schumacher-Eschmeyer, and Chapman or Modified
Schnabel estimators. Formulas and criteria to be considered for the population
estimates were discusse·d on page 16. The three estimates were similar, with
the Chapman estimator showing the best degree of fit (table 13).
TABLE 13. Estimated populations of sauger moving into the lower Tongue River,
spring 1976.
Estimator N 95% Cl
Schumacher-Eschmeyer 3796 3249-4564
Schnab 37la 3136-4542
Chapman 3680 3114-4498
51
HABITAT PREFERENCE
Daily catch rates were totaled for each week of the sampling season. The
data were analyzed in two ways: by catch/kilometer and catch/trip. Calcula-
tion of discharge vs. catch rates was performed as discussed above for
shovelnose sturgeon. The number of fish sampled in certain flow regimens
(discharge-frequency histogra~) is graphed in figure 23. The data points
form only one side of the graph, but, since it can be assumed that there would
be zero fish at zero flow, the other side can be interpolated. It is possible,
however, that there would be zero fish before the flow reaches zero.
The quadratic regressions of trip and linear catch rates in relation to
the discharge resulted in an optimum passage flow est.imate of 13.6 m3/sec
(430 cfs) for both catch rates. Figure 24 indicates very little passage
occurring at flows less than 8m3/sec (280 cfs).
Temperature
The temperature graph (number of fish caught within a specified range of
temperatures) shows a near-normal distribution of sauger moving into the
Tongue River (figure 25). A regression was run between the two catch rates
and maximum and minimum temperatures as was done for the shovelnose sturaeon
(see page 40 for model). A hyperbola with optimum values of 12.4°C (54 F) and
9.4°C (49DF), respectively, for the trip catch rate resulted. For linear catch
rates, the maximum and minimum optimum temperatures were 12.3°C (540F) and
9.30C (49DF), respectively (figure 26). The preferred temperature regimens
found in the Tongue River during the spawning migration correspond to those
found in other areas (Brown 1971, Scott and Crossman 1973).
TAGGING STUDIES
A total of 646 sauger were tagged with Flay anchor tags in 1976. Of
these, 22 (3.4 percent) were returned by anglers. The majority of the tags
(81.8 percent) were returned from the Tongue River. Some local movement was
shown, with many fish moving upstream to the T&Y diversion, 24 to 29 km
(15 to 18 mi) upstream from where they were tagged. Four sauger were caught
in the Yellowstone River, three moving upstream. The downstream migrant
moved about 28 km ( 17.6 mi) in 50 days. Upstream movement ranged as fo 11 ows:
1.6 km (1 mi), 19 days; 84 km (52.4 mi), 78 days; and 164 km (102 mi),
87 days. The range of movement demonstrated by the small sample suggests a
mobile sauger population inhabiting the Yellowstone River. The low tag return
rate by fishermen indicates that the fishery is not being utilized to its
potential.
CHANNEL' CATFISH
The channel catfish (Ictalurus punc~atus) is probably the most sought-
after game fish in the lower Yellowstone River Basin. The channel cat, native
to Montana, was first reported by the Lewis and Clark Expedition. Preferred
52
,
~ .. .. s ......
400
., 300
~
~
a.
0 u
"' ~
u. 200
" ..
D
E
~ z 100
I
I
I
I
I
I
I
I
I
I
I
I
I
I
I
I
1
I
I
/-
o+-----~------~-----c------~~--~
0 5 10 15 20 25
Discharge (m'lsec)
Figure 23. Plot of the quantity of sauger taken per interval of
discharge in the spring spawning migration of 1976 in the Tongue River.
30 Linear Catch Rota Trip Calch Rate
Discharge 60 vs. Discharge YO.
25 ~13.6 m3/sec --50 /13.6 m3/sec
~
/ \ .. ,. '
I \ .. I ' s
I ' ...... I ' ~ 20 I ' ... I \ I \ :s 40 I ......
"' • -..
0
0::
"' u
0
<.>
15
10
5
0
...... \ I \ "' I \ I •
I \ -I I \ I I ~ 30 I I
I I 0 I I
I 0:: I I
I I "' I I
I I u
I I 0 20 I
I <.> I I
I I I I I I I I I I I I I I 10 I I I I I I I I I I I
I I I I
0
10 15 20 10 15 20
Discharge (m3/sec) Discharge (m3/sec)
Figure 24. Quadratic regression analysis of discharge versus catch
rates of sauger collected in the spring of 1976 in the Tongue River.
53
"D
CD
~
:::1 -c.
0 u
~
"' i.L -0
~
CD
.a
E
:::1 z
500
400
300
200
100
25
:! 15
" a: ..,
~
~ 10
0
0 5 10 15
'\
\
20 25
\
\
\
\
Temperature ("C)
\
\
\
\
\
\
30
\
\
\
\
----Maximum
---Minimum
35 40 45
Figure 25. Plot of the quantity of sauger taken per interval
of maximum and minimum water temperatures in the spring of -1976
in the Tongue River.
0
Linear Catch Rate
va. Temperature
9.3°C' _..#"12.3°C "' ...... . . '• I :\ \
I .: \
I .: \
I \
I \
I \
I \
I I
I \
I I
I I
I I
I I
I I
I
5 10 15
Temperature ("C)
-50
~ .. .. • ...... ...
:E 40 ...... .c
D -.. 30 0 a: ..,
u
" 20 0
10
0
20 0
Trip Catch Rate
vs. Temperature
9.4°C~ /12.4°C , ' .. ··. I ... \ I \
I \
I \
I \
\ I I I : I I \ I I
I I
I I :
I I
I I
I I
I I
5 10 15 20
Temperature ("C)
Figure 26. Quadratic regression analysis of maximum and
minimum water temperature versus catch rates of sauger taken in
the spring of 1976 in the Tongue River.
54
50
Minimum
Maximum
r
habitat is large rivers and lowland lakes, but channel cats are not tolerant
of pollution and require well oxygenated water. Spawning occurs from May
into July after water temperatures warm to 240C (75°F), with 26.70C (80°F)
reported as optimum spawning temperature (Brown 1971). Nests are usually
built in secluded, semidark areas around logs, undercut banks, or other
cavities. The channel catfish received game fish status in Montana in 1g75
as the result of legislative action.
FISH SIZE
Length-Weight Relationships
As shown in table 14, catfish taken in 1g75 were smaller than fish taken
in 1975.
TABLE 14. Average lengths and weights of catfish taken in the Tongue River in
1975 and 1976.
1975
Study Section Length (mm)
Ib 401
IIa 493
lib 452
CONVERSIONS: 1 mm = .0394 in
1 g = • 0022 1 b
Age and Growth
1976
Weight (g) Length (mm) Weight (g)
690 375 644
1270 ------
1070 379 596
In 1975, 337 spines were sectioned and aged; 132 were aged in 1976. The
1975 sample was divided into those catfish captured below the T&Y Diversion
(table 15) and those captured between the T&Y and S-H diversions (table 16).
Only fish sampled below the T&Y Diversion were analyzed in 1976 (table 17).
Ages were comparable between years for the section downstream from T&Y
Diversion.
The variation of lengths in a year class increased considerably at 9 years
of age and greater in section Ib and at 13 years of age and greater in
section Ilb in 1975. The average growth per year in section Ib was 1 .4 inches
per year; in section Ilb a pattern of strong growth every other year was
established. In the "good growth" years tne average was 1.6 inches; in the
"poor growth" years the average growth was 0.3 inches.
55
TABLE 15. Average length and range of lengths for each age group of 231 channel
catfish taken below T&Y Dam on the Tongue River in the summer of 1975.
Age Number Average Len~th at Range of Lengths at
Group of Fish Capture mm) Capture (inm)
1 2 127 112-142
2 2B 206 188-221
3 9 229 201-259
4 21 272 226-302
5 17 21B 27g-356
6 19 335 295-381
7 6 373 318-437
8 7 389 353-437
9 22 414 358-599
10 13 450 368-681
11 16 485 411-541
12 29 531 437-660
13 24 531 434-676
14 14 577 470-752
15 3 574 406-665
19 1 752 752-752
CONVERSIONS: 1 mm= .0394 in
TABLE 16. Average length and range of lengths for each age group of 106 channel
catfish taken between T&Y Diversion and S-H Diversion on the Tongue River in
the summer of 1975.
Age Number Average Length at Range of Lengths at
Group of Fish Capture (mm) Capture (mm)
2 1 213 213
4 1 269 269
5 2 305 302-305
6 17 318 297-348
7 2 361 307-411
8 3 363 343-383
9 19 386 323-429
10 7 432 396-475
11 8 446 409-490
12 6 485 447-513
13 10 493 381-570
14 10 541 472-610
15 5 544 49(!-592
16 7 629 574-671
17 3 569 533-617
18 5 612 505-688
CONVERSIONS: lmm= .0394 in
56
TA~LE 17. Average lengths and range of lengths for each age group of 132
channel catfish taken in the lower Tongue River in the fall of 1976.
Age
1
2
3
4
5
6
7
8
9
10
11
12
13
14
15
Sample Size
5
22
14
9
18
2
4
3
4
5
13
13
13
6
1
Average Length (mm)
113
211
251
276
303
340
364
388
447
468
514
547
585
600
743
CONVERSIONS: 1 mm = .0394 in
Range of Lengths (mm)
101-120
186-230
235-279
254-301
274-344
335-344
341"372
362-404
415-477
452-489
456-575
492-665
516-668
374-745
743-743
Those catfish found in section lib were considered to be part of a
resident population since their movement is restricted by the T&Y and S-H
diversions. Since growth rates were constant between years in section Ib,
it is suggested that channel catfish may spawn every other year in section lib.
Meyer (1960) found through examination of annuli on paddlefish maxillary
that the species spawned at intervals of 4-7 years. It is possible that the
irregular growth pattern exhibited in section lib by channel catfish is the
result of alternate-year spawning activity.
OeRoth (1965) found smaller average lengths per age class in the channel
catfish of Lake Erie than those found in the Tongue. The same held true
with the catfish of the Lake of the Ozarks (Marzolf 1955). Witt (1966)
found greater average growth per annulus in the Little Nemaha River. A 9rowth
rate similar to that shown in the Tongue River was found in the Des ~1oines
River of Iowa as reported by Carlander (1969).
CATCH RATES
In 1975, 472 channel catfish were captured in 106 trap sets for a catch
rate of 4.45 fish/trap. Catch rates for the three reaches were: section Ib
57
(Keogh), 4.70 fish/trap (349 in 74 sets); section Ila (Orcutt's),2.00 fish/.trap
(24 in 12 sets); and section lib (S-H), 4.95 fish/trap (99 in 20 sets). Catch
rates in 1976 were lower, averaging only 2.34 fish/trap (138 catfish in
59 trap sets). Traps were fished in sections Ib and lib in 1976; catch rates
were the same in the two sections. Reduced flow levels and unusually high
summer temperatures probably resulted in the lower catch rates.
TAGGING STUDIES ·
A total of 397 catfish were tagged in 1975, and 103 were tagged in 1976.
Tag returns in subsequent trap·sets averaged 6.3 percent in 1975 and 3.9
percent in 1976·. Anglers returned 3.6 percent of the channel catfish tagged
(18 of 500). Of those tagged in 1g75, 5 (1.3 percent) were returned in 1g75
and 10 (2.5 percent)were returned in 1976 for a total return rate of 3.8
percent. Only 3 (2.9 percent ) of the fish tagged in 1976 have been returned
by fishermen.
Movements of fish tagged in the Tongue River were varied. Eight (44.4
percent) of the returned fish were returned from the Yellowstone River rather
than the Tongue River (table 18). Two of the fish tagged in i975 and
recaptured in 1975 were caught in the Yellowstone. One fish was taken at the
confluence of the Yellowstone and Missouri rivers, about 303 km (188 mi)
downstream from where it was tagged. Only one of the fish recaptured in the
Yellowstone moved upstream after leaving the Tongue. Of the fish recaptured
in the Tongue River, 50.0 percent (5 of 10 fish) were recaptured in the
area where they were tagged. Four of these fish were recaptured the same
year they were tagged. All fish taken in the Tongue River that showed move-
ment ·showed upstream movement, but the eight that were returned from the
Yellowstone River obviously moved down the Tongue before entering the
Yellowstone.
INSTREAM FLOW REQUIREMENTS OF INDICATOR SPECIES
All fish, wildlife, and other aquatic organisms are dependent upon the
natural flow regimen of a river system. Fish production in rivers depends
upon the maintenance of spawning and rearing areas, sufficient shelter,
adequate food supply, and water quality. The stream discharge, as influenced
by channel configuration, must meet the hydrologic requirements necessary
to provide these factors.
The State Water Planning Model simulated monthly streamflow conditions
which would result from the implementation of several levels of agricultural
or industrial development. Monthly Tongue River subbasin outflows and total
dissolved concentrations estimated by the model provided the basis for pre-
dicting impacts on the fisheries. Four levels of industrial and three
levels of irrigative withdrawals were considered.
As explained on page 17 , potential impacts were assessed on the basis
of the effect on flows associated with three life-history stages of fish--
passage, spawning, and rearing.
58
r
TABLE 18. Summary of angler returns of tagged channel catfish, Tongue River,
1975-76.
Tagged
Tag Number Date Locationa
1007 8/6/75 TR-Ib
1021 8/6/75 TR-Ib
1022 8/6/75 TR-Ib
1024 8/6/75 TR-Ib
1053 8/8/75 TR-Ib
1075 8/13/75 TR-Ib
1104 8/14/75 TR-Ib
1124. 8/17/75 TR-Ib
1132 8/17/75 TR-Ib
1136 8/20/75 TR-Ib
1144 8/20/75 TR-Ib
1157 ~/22/75 TR-Ib
1181 8/22/75 TR-Ib
1202 8/22/75 TR-Ib
1340 9/17/75 TR-IIb
3/23/76 TR-Ia
1372 5/7/76 TR-Ia
2394 3/31/76 TR-Ib
2982 7/29/75 TR-Ib
a YR = Yellowstone River
TR = Tongue River
MR = Missouri River
Recaptured
Date Locationa
5/22/76 YR
9/8/75 YR
9/14/75 TR
8/19/75 YR
8/19/75 TR
8/14/75 TR
8/ll /76 YR
7/10/76 YR
3/29/76 YR
7/27/76 MR
4/7/76 TR
8/ll/76 YR
6/5/76 TR
9/18/76 TR
10/19/75 TR
9/6/76 TR
8/5/76 YR
5/21/76 TR
5/22/76 TR
b + designates upstream movement and -downstream.
Movement
( km)b
+3.2c
-70.0C
0
-9.7C
0
0
-4.8C
. -l.OC
-8.1C
-302.5C
0
+8.1 c
+29.0
+29.0
0
+29.0
-11.3d
0
+29.0
c These fishes moved downstream 1.5 km in the Tongue River before reaching
the Yellowstone.
d This fish moved downstream 0.5 km in .the Tongue River before reaching
the Yellowstone.
Indicator species selected by Bovee (1974) for ·passage and spawning
flows were paddlefish (larger rivers) and sauger (smaller streams). However,
for the Tongue River, shovelnose sturgeon were substituted for paddlefish
because of greater abundance. Channel catfish were added because they
migrate and spawn later in the season.
59
PASSAGE AND SPAWNING FLOWS
Sauger are found moving out of the Yellowstone into the Tongue from
March to June. According to Bovee (1974), the spawning depth criteria
for sauger is 1.2-1.5 m (3.9-4.9 ft). Since it is assumed that if passage
criteria are met then spawning criteria are also met, the converse was also
assumed to be true. Therefore, only one flow level is recommended to meet
the needs for both passage and spawning. Based on pred~cted flow conditions
from the WSP program, flows ranging from 19.8 to 48.9 m /sec (700-1725 cfs)
would provide adequate passage and spawning depths. The minimum sustaining
discharge is defined as 75 percent of optimum (Bovee 1974). The recommended
minimum passagj and spawning flow for sauger for the months of March through
June is 14.9 m /sec (525 cfs).
The spawning migration of the shovelnose sturgeon commences around the
first of May. Depth requirements for shovelnose sturgeon are reported as
0.3-0.9 m (1 to 3 ft) (Bovee 1974). Sampling of shovelnose in the lower
Tongue River revealed that nearly 80 percent of the fish sampled were taken
in depths ranging from 0.6 to 1.0 m (2 to 3.3 ft). Based on WSP predicted
flows, discharges of 23 to 62 m3/sec (800-2200 cfs) are required to meet
shovelnose sturgeon criteria. The recommended flow for shovelnose sturgeon
during May, June, and half of July is 17m3/sec (600 cfs).
Channel catfish spawn at temperatures ranging between 23.9 and 29.5°C
(75-850F). Water temperatures in the Tongue River generally reach these levels
during June, July, and August. Therefore, requirements for this species
are established for this time period. Spawning depths for catfish have not
been determined, but Bovee (1974) reported depth preferences ranging from
0.31 to 1.53 m (1.0 to 5.0 ft). Using WSP predicted flows for pool areas,
flow ranges of 8.5 to 21 m3/sec (300 to 750 cfs) were established. Baseg on
75 percent of optimum, the recommended flow for channel catfish is 6.4 m /sec
(225 cfs).
REARING FLOWS
Rearing flows are needed during the remainder of the year. Dewatering
will more severely affect areas of shallow, fast water than areas of deep,
slow water. If these shallow areas are maintained, then the stream will
be protected. Rearing flow recommendations are based upon the assumption
that rearing is proportional to food production, which is in turn assumed
proportional to wetted perimeter (White and Gochnauer 1975). Wetted perimeter
was determined for several transects based on WSP predicted flows. Starting
at zero discharge, wetted perimeter increases rapidly for small increases in
discharge up to the point where the river nears its maximum width. Beyond
this inflection point, wetted perimeter increases slowly while discharge
increases rapidly. The optimum quantity of water for rearing is selected
near this inflection point (figure 27). Optimum flow value for the Tongue
is 7m3/sec (250 cfs), so the recommended minimum flow value (75 percent of
optimum) is 5.4 m3/sec (190 cfs). Bovee (1975) suggested using the stonecat
as a rearing flow indicator species. The stonecat was selected for its
preference of fast, shallow water areas. Stonecats sampled by Bovee in the
Tongue River showed a marked depth preference ranging between .30 and .60 m
60
1
-
70
60
50
E
~ ., 40 -"' E ·;: .,
a.
"1:1 30 ., --"' .,
~ ~
20
10
0
0
/
/
.,.. -----
Illb
-----------------------------rb
/ -t llb //~.--·····································-···························································································································
/.······ ,..
I
}
!/
il
! I
it
'I
I
I
5 10
.,
15 20 25 30 35 40
Discharge (m3/sec)
Figure 27. Wetted perimeter in relation to discharge for three sections of the Tongue
River, showing the inflection point used to determine rearing flows.
45
(1 and 2 ft). Using WSP predicted flows for riffle transects, the flows at
these depths range from 6.8 to 17 m3/sec (240 to 600 cfsl. Using 75 percent
of.optimum, a minimum rearing flow recommendation of 5m3/sec (180 cfs) is
obtained.
MONTHLY INSTREAM FLOW REQUIREMENTS
Recommended minimum instream flows shown in figure 28 are the flows
necessary for the species with the highest requirements for each month.
While the instream flows presented for each life history stage and each
species are 75 percent of the optimum value, a flow was not recommended
unless judged to be an adequate flow. Professional experience was utilized
as a basis for determining if a flow was adequate.
62
,
01 w
Jan Feb Mar Apr May June July Aug Sept Oct Nov Dec
SAUGER
-~-~
spawning 14.9 "'
~ -
rearing
-------·------' -c .. --_, -. --~ --' ~ ', ' --
5.4 5.4
~ ,, .. ,_.. --'' ~' -----------------------~ -~ _,
SHOVELNOSE STURGEON
spawning
------------------,
17.0 ---·
CHANNEL CATFISH
spawning ----~---·---------,,,.~
6.4 ----------' '~'
____ ,_-----
,_,_,,_, __
rearing 5.4 ~_.4 ·-------
STONE CAT
-· -,. ~-.. rearing 5.1
RECOMMENDED FLOW 5.4 5.4 14.9 14.9 17.0 17.0 % 4 6.4 5.4 5.4 5.4 5.4
MEAN NATURAL FLOW 5.3 7.8 18.7 15.4 23.3 45.5 14.6 4.5 5.8 8.1 8.8 6.1
LEVEL OF DEVELOPMENT
low 4.8 8.8 22.0 14.5 25.5 48.9 9.4 1.5 2.1 3.7 4.8 4.8
intermediate 1.8 4.4 15.2 9.1 18.1 42.5 5.1 1.8 1.2 1.6 1.6 1.5
high 1.6 3.6 14.5 8.7 16.5 39.9 4.6 2.3 1.5 1.6 1.6 1.5
All values expressed in m3/sec
Figure 28. Life history periodicity and minimum flow recommendations for selected
species and projected flow values for the Tongue River from the T&Y Diversion to the mouth.
THE NATURALLY OCCURRING PATTERN OF LOW FLOWS
Because the aquatic biota of the Tongue River has developed in response
to both high and low flows, the frequency and magnitude of naturally occur-
ring low flows was examined. Shown in table 19 is a summary of historic
flows and low-flow occurrences of the Tongue River near its mouth for the
years 1931-75. Although this report refers to naturally occurring low flows,
the term is misleading because l) flows of the Tongue River are regulated
by Tongue River Dam, and 2) the gaging station is located downstream from
the lowermost irrigation diversion.
When comparing naturally occurring low flows in the Tongue with those
that would occur after the projected levels of development, it is necessary
to distinguish between basin outflows at the mouth of the river and
instream flows occurring immediately below the Tongue River Dam. Because
both the agricultural and industrial development projected would rely on
increased storage, more water would be released during low-flow periods
for downstream use. Hence, at least for the portion of the river just
below the dam, instream flows after development would probably be high and
more constant through the year (since release for industrial use would not
vary) than are existing flows. However, those additional releases of water,
plus much of the existing flow, would be diverted and consumed along the
course of the river; at the river's mouth, flows after development would be
much lower than are naturally occurring low flows, resulting in the severe
impacts described in tables 20 and 21 as opposed to the lesser, naturally
occuring impacts described in table 19.
Naturally occurring low flows also result in high TDS concentrations.
Four months (October-January) commonly show levels greater than 700 mg/1.
Two months, December and January, occasionally reach 1000 mg/1. However,
these concentrations do not occur at critical fish life-history stages, and
little impact occurs.
IMPACTS OF INCREASED FUTURE USE
PROJECTIONS OF FUTURE USE
In order to adequately and uniformly assess the potential effects of
water withdrawals on the many aspects of the present study, it was necessary
to make projections of specific levels of future withdrawals. The methodology
by which this was done is explained in report No. l in this series, in which
also the three projected levels of development, low, intermediate, and high,
are explained in more detail. Summarized in appendix A, these three future
levels of development were formulated for energy, irrigation, and municipal
water use. Annual water depletions associated with the future levels of
65
"' "'
TABLE 19. Surnr~ry of historic flows (1931-75) on the Tongue River as related to recommended instream flows by season.
Season Flows and Impacts
Fall
Winter
Spring
Runoff
H1stonc Flows
This season normally shows the year's lowest flow levels
due to reduced streamflow and to irrigational demands
in August. For the entire season, flows fall below,the
1nstream requests 49.3 percent of the time. Water
temperatures may become intolerable for many resident
fishes. In August, instream flow requests would
have been met only 20 percent of the time. October
and November show adequate flows over 70 percent
of the time.
This low-flow period is not influenced by irrigation
demands. Still, one year out of two has flows below
instream requests, resulting in riffle freeze-up
and decreased oxygen levels.
Most erratic flow petiod; natural flows fall below
instream requests 53.8 percent of the time.
Naturally occurring flows fall below recommended
instream levels only 24.3 percent of the time.
Natural impacts are lowest during this period.
Low Flows
Critically low flows (those that provide less than half of
the recommended instream levels) occur one out of every four
years, resulting in reduced wetted perimeter and lowered
velocities. In August, one out of two years shows extremely
lm< flows. Most dry years are followed by two or three wet
years, preventing long series of dry years.
Extreme low flows occur only 5.9 percent of the time.
One year out of four exhibits extremely low flows, reducing
spawning habitat for sauger.
Extremely low flows affecting spawning and passage of
paddlefish and sturgeon occur once every eight years.
NOTE: Impacts described by the percentage of time they would occur may be interpreted as occurring by the year rather than by the day.
For example, an impact described as occurring 90 percent of the time would occur nine years out of ten, on the average.
1
development were included in the projections. These projected depletions,
and the types of development projected, provide a basis for determining the
level of impact that would occur if these levels of development were carried
through.
IMPACTS OF REDUCED STREA~1FLOW
Agricultural Projection
Mean flow values for each projected level of development are compared with
recommended instream flows and mean monthly natural flows in figure 28.
Possible impacts associated with each development level are presented in
table 20. Frequencies of low flow are relative to the 30-year period of flow
records.
Fall. August flows for the low level of agricultural development would
fall critically short. Flows necessary to ensure adequate channel catfish
spawning during August are 6.4 m3fsec (225 cfs); only one year in 30 showed
enough water to maintain this flow. Low flows to 1m3/sec (36 cfs), which
would drastically reduce wetted perimeter, lower velocity, and reduce depth,
would result nearly 90 percent of the time (26 of 30 years).
Flows resulting from the intermediate level of development would fall
short of channel catfish requirements all years. One year shows almost enough
water but is still short. Flows associated ~lith the high development level
fall short all years and would decimate channel catfish spawning in this
reach of the Tongue River.
September flows would be similar to those for August. With the low
development level, flows would be adequate to meet rearing requirements only
one year out of six. Intermediate and high development level flows would be
inadequate in all years.
Low-development-level flows for October and November would be adequate
for rearing one year out of four and one year out of two, respectively.
Intermediate and high levels of development, however, would result in depleted
flows at least nine years out of ten.
In summary, agricultural development would have its greatest impact on
the fishery of the Tongue River during the fall months, since August and
September are months of normal low flows and high irrigation use.
Winter. The low level of development would result in low flows one
year out of two for December and January and one year out of 1.4 for February.
The impacts would probably be minimal, however.
As with the fall period, both the intermediate and high levels of
development would be expected to result in severe impacts for December and
January. At least 85 percent of the time, rearing flows would not be main-
tained for these months. The intermediate projection would provide adequate
flows one year out of 4.3 in February, but the high projection would have
a severe impact in that month.
67
"' CD
TABLE 20. Predicted impacts of three agricultural development levels on the flow of the Tongue River.
Fall
Winter
Spring or
Spawning
· Runoff
Low
Low flows, no channel catfish
spawning, reduced wetted peri-
meter, lower velocity, reduced
depth 90% of time, rearing
flows adequate an average of 1
out of 4 years. Greatest impact
on fishery during this time of
year.
1 year out of 2 with low
rearing flows. Impact
minimal.
Low flows during July
(2 out of 3 years). Reduction
of egg survival. High temper-
ature: Impacts minimal
Impacts minimal.
Intermediate
Same impacts as low development, plus
rearing flows are inadequate at
least 9 out of 10 years. Greatest
impact on fishery during this time
of year.
Rearing flows not maintained 85%
of time. High impact on fishery
would result.
April would have inadequate flows
76.7% of time. Loss of sauger
spawning habitat and reduction in
shovelnose sturgeon egg survival.
High impacts on sauger and shovel-
nose sturgeon in Tongue.
Flows in July would be moderate
83.3% of time, resulting in loss
of shovelnose sturgeon spawning
habitat. High impact on shovel-
nose sturgeon and channel catfish.
High
Same impacts as intermediate
development.
Severe impact on fishery.
Rearing flows inadequate
especially during February.
Flows inadequate 85% of
time for rest of the months.
Impacts similar to intermed-
iate scenario. Severe impact
on shovelnose sturgeon and
sauger fishery.
Inadequate flows during July
would occur 90% of time,
resulting in serious loss of
shovelnose sturgeon and channel
catfish spawning potential.
Severe impact on shovelnose
sturgeon and channel catfish
fisheries.
NOTE: Impacts described by the percentage of time they would occur may be interpreted as occurring by
the year rather than by the day. For example, an impact described as occurring 90 percent of the time would
occur nine years out of ten, on the average.
'
Spring. The low level of development would have little impact on the
fishery of the lower Tongue River. July would be the month of the highest
impact, with inadequate flows two out of three years. Low flows during
this period would result in excessive water temperatures which would be
detrimental to sturgeon egg hatching. Predicted flows for May and June would
have little or no negative impact. For sauger spawning, flows in March would
be inadequate one out of two years and April flows would be inadequate
67 percent of the time. The impact during these months would probably be
minimal.
At the intermediate level of development, July flows would be inadequate
83.3 percent of the time, resulting in high water temperatures, reduction in
egg survival, and loss of spawning habitat. Impacts would be minor in May
and June. April flows would be inadequate 76.7 percent of the time (23 of
30 years). This flow reduction would result in loss of habitat, loss of
wetted perimeter, and loss of depth and velocity needed for sauger to spawn.
The impacts during March would be similar to those of March under the low
projection.
The effect of the high level of development during the spring spawning flows
would be similar to that of the intermediate level with the exception of July.
During July, flows would be insufficient 90 percent of the time, with impacts
similar to those described previously. This would seriously affect shovelnose
sturgeon spawning in the lower Tongue River.
Summary of Impacts. With the low level of agricultural development,
there would be little impact except during fall. With the intermediate and
high levels of development, there would be severe impacts on the fishery
during the entire year, resulting in the loss of spawning and rearing flows
necessary to maintain the sauger and channel catfish fishery. There would
be a severe loss of spawning habitat for the shovelnose sturgeon during the
spring (runoff) flows.
Industry Projection
A summary of possible impacts associated with each development level is
presented in table 21.
No major impact associated with the low level of development could be
predicted to occur on the Tongue River.
Impacts predicted for the intermediate level of deyelopment would be
greatest during the spring, when an estimated 500,000 mZ (5.4 million ft2) of
potential spawning habitat would be lost downstream from the T&Y Diversion.
Winter flows less than 2.5 m3/sec (90 cfs) would result in icing on riffles
and, therefore, invertebrate losses (Bovee 1976). This would occur about
20 percent of the time at this level of development. These flows would
adversely affect the fishery.
The intermediate development level, even with 60 percent of NGPRP
instream flows (NGPRP 1g74) guaranteed, would still have high impact. In many
years there would be little or no flow in the river during the fall, and
69
......
0
TABLE 21. Summary of predicted impacts of three projected levels of industrial development of Tongue River water.
Season
Fall
Winter
Spring
Runoff
low
little impact,
possible high
temp. during
Oct. (2.5% of
the time).
No impacts other
than those
occurring nat-
urally .
No impacts
other than
those occur-
ring naturally.
No impacts
other than
those occur-
ring naturally.
Intermediate
Possible impact:
8 years, no flow;
2 years, possible
temp.
1 out of
1 out of
high
Possible impact: 2 out of
9 years, ice would form on
riffles, with possible
o2 depletion.
Possible impact: 4 out of
10 years, spawning habitat
reduced; 1 out of 10 years,
inadequate flows; 1 out of
30 years, no flow.
Possible impact: 1 out of
4 years, no bedload move-
ment, loss of scouring;
30~ of time no flow;
some possible high temp.
problems.
Intermediate
(60% NGPRP)
High impact: 1 out of
3 years no flow; over 90%
of the time, possible
problem with high temp.
High impact: 4 of 5
years riffles would
freeze, with probable
02 depletion.
Possible impact: 3% of
time, no flow; spawning
habitat reduced greatly
all years.
High impact: over 30%
of time, no flow; just
under 30% of the time,
flow inadequate for
paddlefish spawning;
high temp. problems
possible also.
High
Extreme impact: 98% of the
time, no flow; remainder of
flows inadequate to support
fishery.
Extreme impact: over 90%
of the time, no flow; 2%
of time, adequate flows.
High impact: almost 70%
of the time, no flow; remain-
inq years flows inadequate
and spawning habitat lost.
Extreme impact: over 60%
of the time, no flow; almost
20% of the time, flows would
be inadequate.
NOTE:" Impacts described by the percentaqe of the time they would occur may be interpreted as occurring by the
year rather than by the day. For example, an impact described. as occurring 90 percent of the time would occur
nine years out of ten, on the average.
riffles would freeze during the winter. Approximately 650,000 m2 (7 million ft2)
of potential spawning habitat would 'be lost during the spring downstream from the
T&Y Diversion. During run-off, no flow would be present about one-third of
the time. Paddlefish would be unable to migrate upstream about one-fourth of
the years in which there would be measurable flow. With these flow levels,
there would be a minimal fishery downstream from the T&Y Diversion.
With the high projection, flows would be almost nonexistent downstream from
the T&Y Diversion, and impacts would be extreme.
Since that portion of the river downstream from the T&Y Diversion pro-
vides a spawning and nursery area for fish from the Yellowstone River, a
reduction in flows would also adversely· affect the Yellowstone River fish
population. Thus, impacts on the Yellowstone River fishery as well as on the
Tongue.River fishery would occur from reduced flow in the Tongue.
IMPACTS ON WATER QUALITY
The impacts of reduced flow on water quality were evaluated in terms of
total dissolved solids (TDS) concentrations (salinity). Concentrations of
TDS ranging from 670 milligrams per liter (mg/1) to a maximum of 1350 mg/1
were considered the range for a good, mixed fishery in western alkaline
streams (Klarich 1977). Some minor adverse effects would be expected at
concentrations over 670 mg/1, becoming more severe as concentrations
approached and exceeded 1350 mg/1. Therefore, TDS levels greater than
700 mg/1 were considered to have an impact on the fishery.
Fall
Four months (August-November) would have TDS greater than 700 mg/1 with
the low level of development. August levels could be high enough to deter
channel catfish migrations. With the intermediate level of development, all
months _would be greater than 700 mg/1; August through December would be
greater than 1,000 mg/1. Channel catfish migration and spawning in August
could be affected. All months would show levels greater than 1,000 mg/1
with high development. Impacts would be the same as with intermediate
development.
Winter
December and January would have TDS concentrations greater than 700 mg/1
with.low development, and all winter months (December-February) would have
greater than 700 mg/1 with intermediate development. December showed con-
centrations greater than 1 ,000 mg/1 under both intermediate and high development.
However, impacts should not be significant during this period.
Spring
No impact would be expected with low or intermediate development.
high development, March and April show TDS concentrations greater than
which could affect sauger migration and spawning.
71
Under
700 mg/1 ,
Runoff
The low levels of development would have no water quality impact. July
would show concentrations greater than 700 mg/1 with the intermediate and
high levels of development, which could affect channel catfish migration
and spawning. The end of the shovelnose sturgeon and paddlefish runs could
be affected, as could egg incubation.
OTHER LIMITING FACTORS
Thus far, discussion of impacts of future water withdrawals on the
aquatic biota of the Tongue River has been limited to the impacts of low
flows. Low flows result in decrease in depth, loss of physical habitat,
reduction in velocity, and deterioration of water quality, all of which
render the habitat less appealing. There are other factors associated with
the lotic community which must be considered.
Temperature
As water levels are lowered, the heat budget of the stream is altered,
and temperatures increase until an equilibrium (between standing water and
the ambient air temperature) is reached. Temperature is a major limiting
factor because aquatic organisms often have narrow tolerances. The life
cycles of fish and invertebrates, day length, and water temperature are so
interdependent that even a small change in temperature can have far-
reaching effects. In an artifically warmed stream, insects or fish may
hatch too soon to fit into the food chain and successfully compete. If
temperatures are near the upper limits of tolerance, the fish will be placed
under stress if not killed. Similar competitive disadvantages would result
with a cooling of water.
Turbidity
Suspended materials limit the penetration of light, restricting
photosynthetic activity. Sediment fills the interstices between gravel,
thereby eliminating spawning areas and aquatic insect habitat. The ability of
a stream to move this material and hence cleanse the stream bottom depends on
the discharge, particularly during the spring runoff. Low flows reduce
bedload movement and thereby limit fish production.
Concentration of Respiratory Gases
Oxygen and carbon dioxide concentrations are often limiting to the
aquatic community. As flows are reduced and temperatures increased, concen-
trations of oxygen become critical. Eggs are especially vulnerable to
oxygen lack because they depend upon oxygen diffusing into them at a rate
sufficient to maintain the developing embryos.
72
An excess of "free" carbon dioxide may have adverse effects on aquatic
organisms, ranging from avoidance reactions and changes in respiratory move-
ments at low concentrations, through interference with gas exchange at higher
concentrations, to narcosis (unconsciousness) and death if the concentration
is increased further. According to the Federal Water Pollution Control
Administration (1968) respiratory effects seem most likely of these impacts
to be of concern.
Concentration of Salts
Fresh-water fish have a problem in regard to osmoregulation. Since the
concentration of salts is greater in the internal fluids of the body than in
the fresh-water environment, then either water tends to enter the body by
osmosis if membranes are readily permeable to water or salts must be con-
centrated if membranes are relatively impermeable (Odum lg64). Increases
in salts (TDS) may create a problem in fish habitat preference. The
possibility exists of a barrier to migration being produced by a zone of
high TDS concentration. Reduction in flow could produce a TDS problem by
concentrating salts and by reducing the diluting force of the stream.
LIMITING FACTORS UNRELATED TO FLOW
Several factors not dependent upon discharge may also have an impact on
the fishery of the Tongue River. These are: 1) fishing pressure, 2) land
use practices, and 3) pollution.
Fishing pressure is an environmental factor which may be manipulated
to increase both fish production and yield. Pressure is often too great
or too small, in relation to the productive capacity of a stream, to give
maximum yield. Tag returns from the Tongue River suggest that pressure
and harvest are light. Therefore it is doubtful that this factor results in
a significant impact on the fishery.
Land use practices such as overgrazing, cultivation of the floodplain,
and channel disturbances all can produce a negative impact on the fishery
by degrading the habitat. Stream-bank stability can be destroyed through
overgrazing and many other agricultural activities, resulting in bank
sloughing and siltation. Channel disturbances reduce spawning and food-
producing areas, and stream realignment shortens the total length of the
river. Land use practices along the Tongue River have historically pro-
duced examples of the above impacts. Future practices should not signifi-
cantly increase problem areas.
The final factor, pollution, could possibly result from introduction
of an allochthonous, toxic substance, such as an effluent from a steam
generating plant containing substances harmful to the fish. Even if the
materials were not in toxic concentrations, the basic fertility of the
river could be altered, favoring another assemblage of fish species. An
alteration of the natural heat budget of the river is another possible
impact from coal conversion complexes. Since the Tongue River Basin has
been identified as a potential site for such complexes, this impact looms
as a threat.
73
.s~
A study was conducted on the Tongue River from 1974 to 1976 to determine
fish species composition, distribution, and diversity and to evalute impacts
of water withdrawals on the river system. Distribution of the 31 fish species
taken in the Tongue River was found to be influenced by irrigation structures.
Species migratory from the Yellowstone were restricted by the T&Y Diversion,
22.7 km upstream from the mouth. Smallmouth bass were the dominant resident
game fish. Discharge patterns from the Tongue River Dam affected the
reproductive success of the smallmouth bass population. Species diversity
indices generally increased with progression downstream and appear to be a
useful tool in describing the fishery of a prairie stream.
Migrant fish populations using the lower Tongue River were monitored.
Shovelnose sturgeon moved into the Tongue River from the Yellowstone River
during April, May, and June in 1975 and 1976. The majority of the sturgeon
sampled were between 710-785 mm in length in 1975 and 725-800 mm in 1976.
Compared with a spring sample taken on the Yellowstone River at Intake, the
Tongue River fish were considerably larger. Weights to 6 kg, larger than
shovelnose reported in other areas, were not uncommon. Schnable-type
population estimates showed 400-500 sturgeon/km present during the spring
runs both years. Quadratic equations comparing number of fish with dis-
charge and temperature documented passage preferences. It appears from those
regressions that a minimum discharge of 8.50 m3/sec is necessary for shovel-
nose sturgeon passage and that the optimum temperature range for sturgeon
spawning is from 16.90C to 21.soc. Fish tagged with monel bands on the
pectoral fin lost weight between the times of tagging and recapture; those
tagged with Floy anchor tags gained weight. Angler harvest of sturgeon in
1974-76 was light.
Sauger were sampled during April and May of 1976; 1,004 fish averaged
377 mm in length and 441 g in weight. A preferred passage flow for sauger
was estimated at 13.6 m3/sec using a quadratic regression of catch rate
against discharge. Population estimates showed around 3,700 sauger moved into
the lower river in 1976. The optimum temperature range for sauger spawning
migration was from 9.3°C to 12.40C. Tagging studies indicated that the
Yellowstone River sauger population is mobile and underutilized by fishermen.
Channe 1 catfish were sampled with baited traps both years. In 1975,
average lengths of catfish from the three river study sections sampled ranged
from 401 to 493 mm, and average weights from 690 to 1270 g. In 1976, fish
were smaller; average lengths ranged from 375 to 379 mm and average weights
from 596 to 644 g. Pectoral spines were taken, sectioned, and analyzed for
age and growth. Tag returns by anglers of sturgeon, sauger, and catfish
were low and suggested an underutilized resource.
Recommended flows for passage and spawning of three indicator species--
sauger, shovelnose sturgeon, and channel catfish--were determined in order
75
to allow assessment of the impacts of lowered streamflow on fish populations.
The recommended minimum passage and spawning flow for sauger from March through
June is 14.9 m3/sec. For shovelnose sturgeon, the recommended flow for passage
and spawning for May, June, and half of July is 17 m3/sec. Channel catfish
spawn in the Tongue River in June, July, and August; the recommended flow
for this species is 6.4 m3/sec. For the remainder of the year, it is
recommended that rearing flows of 5 m3/sec (the recommended flow for rearing
of stonecats) be maintained.
It is the naturally occurring flow regime, including low flows, that has
resulted in the existing aquatic biota of the Tongue River. That naturally
occurring pattern of low flows is described in this report and compared with
the predicted flows after each of three future levels of development. Compari-
son of the predicted post-development low flows at the mouth of the river with
the recommended passage and spawning flows given above shows that even for the
low level of development, fall flows would not supply the recommended channel
catfish spawning flow. Lowered flows resulting from the intermediate level
of development would have a severe impact on all indicator fish species. At
the high level of development, flows would be almost nonexistent downstream
from the T&Y Diversion, and impacts on the fishery would be extreme. Water
quality would also be affected by agricultural and industrial development
and water use in the Tongue River Basin, with some adverse effect on the
fishery. The potential alteration of other limiting factors, such as
temperature, pollution, and turbidity, among others, is also discussed.
76
~J 11
by
Allen A. Elser
Robert C. McFarland
77
PURPOSE
The objectives of this segment of the study are: (1) to inventory the fish
populations of the Tongue River Reservoir so that changes associated with coal
development can be detected and, if necessary, mitigative measures taken; (2) to
determine angler use and harvest of major sport fish in the Tongue River Reser-
voir; and (3) to evaluate possible impacts associated with large-scale withdraw-
al projects.
STUDY AREA
Flow of the Tongue River in Montana is controlled by the Tongue River Dam,
behind which lies the Tongu~ River Reservoir. The earthfill dam, completed in
1940, impounds over 84.9 hm (69,000 af) of water with a surface area of 1,416
ha (3,500 acres). Firm annual yield is 49.2 hm3 (40,000 af). Sheridan, Wyoming,
the nearest city, is located approximately 32 km (20 mi) south of the reservoir.
The dam is 13 km (8 mi) north of the Montana-Wyoming state ~ine (see figure 1 on
page 3 ) , impounding water from a drainage a rea of 4403 km ( 1, 700 mi Z).
Decker Coal Company, a subsidiary of Peter Kiewit Sons' Co., began mining
coal near the Tongue River Reservoir in 1973. Over 3 million tons of coal were
removed by Decker in 1973; the 1976 level of production was 10.3 million tons.
Currently, mining operations are confined to the west side of the reservoir,
but Decker is expanding (subject to permit approval) to the north of current
operations and to the east side of the reservoir (figure 29). When these ex-
tensions are in operation, the Decker operation will be the largest producing
strip mine in the world, with an estimated annual production of 14.5 million
tons by 1980.
The Tongue River and Tongue River Reservoir may be increasingly important
in light of proposed coal development. While most coal mined in r~ontana now
leaves the state, additional coal conversion plants (for example, for steam-
fired generation, gasification, and liquefaction) close to the coal source have
been proposed. Such energy complexes require great amounts of water, and the
· Tongue is considered an important source of industrial water. Montana Power
Company took an annual option on 5.15 hml (4,175 af) of Tongue River Reservoir
water in 1972. A generation plant in Wyoming which would utilize Tongue River
water has been suggested.
However, water for industrial development in the Tongue River Basin would
not be firmly available without additional storage. In a 1969 study, Bechtel
Corporation considered a new Tongue River dam site about 10 miles downstream
from the existing site. Stage 1 of the proposed res~rvoir, flooding land in
Montana only, would ha~e an active storage of 395 h~ (320,000 af) and firm
annual yield of 120 hm (100,000 af). Stage 2 of the proposed reservoir, be-
79
cr .. l
(Proposed)
WEST DECKER
MINE AREA
(Ex i a tin g)
EAST DECKER
MINE AREA
(Proposed)
0 I 2 Kilomelers
~U=-W:UI:::U::U::====ll
0 2 Miles
tt-j=i--tt=j~--~========~1
Figure 29. Tongue River Reservoir, Montana, showing zones and
sampling stations.
80
cause it would flood land in Wyoming, is not considered likely in the foresee-
able future. Raising the existing dam could provide a maximum storage of 170
hm3 (140,000 af) and firm annual yield of 90 hm3 (72,000 af) (Montana Department
of Natural Resources and Conservation 1976).
81
SAMPLING FOR WATER CHEMISTRY ANALYSIS
Water samples were collected from the Tongue River Reservoir on a biweekly
basis from icemelt until freeze-up (Hhalen and Leath 1976). Samples were taken
at three sites in the reservoir (figure 29), from the river above and be 1 0~1 the
mine discharge, and below the dam. Mine discharge samples were also taken. Re-
servoir samples were collected at two-meter intervals throughout the water col-
umn at all three stations with a four-liter Van Darn Bottle. Additionally, sam-
ples were collected at one-meter intervals throughout the euphotic zone for phy-
toplankton standing crop and primary production estimates. Whalen and Leath
(1976) summarize the analytical procedures used for water chemistry analyses.
FISH SAMPLING
Fish were collected using: 4-foot-by-6-foot frame trap nets with 1/2-inch
and 1/4-inch mesh webbing and 50-foot leads; 125-foot experimental gill nets; a
100-foot, 1/4-inch-mesh beach seine; and a 50-foot, 1/4-inch-mesh bag seine. An
electrofishing boat equipped to provide an output of 0-500 volts variable direct
or alternating current was used to sample shoreline areas. Fish were also taken
with a hook and line. Lengths and weights of captured fish were recorded, and
sport fish were tagged with numbered Flay anchor tags. Scales were taken for
analysis of age and growth.
POPULATION ESTIMATES
Population sizes of black and white crappie and northern pike were esti-
mated from fish captured during the spring trap-net season. The modified
Schnabel estimator was used (Chapman and Overton 1966), employing the expression:
where:
CtMt
Rt +
N =
ct =
Mt =
Rt =
estimated fish population
number of fish caught
marked fish at large
number of recaptures
Confidence limits (a= 0.05) were computed according to the formula:
-L CtMt -P {x < ~ < x )= 1 -a
- N -.t
where~ and x are the lower and upper confidence limits, respectively, of the
Poisson variable, obtained from the table of expectations of Poisson variable
83
(Chapman and Overton 1966). Captured fish· were taken to the midpoint of each
zone prior to marking and released to prevent introducing a bias into the es-
timate.
CREEL CENSUS
A partial creel census designed to sample anglers as they left the reser-
voir was conducted in 1975 and 1976. A creel census station was established
on the main access road to the reservoir (figure 2g) and was operated from
10:00 A.M. until dark or until all fishermen had left the reservoir. Signs
instructing fishermen to· stop were erected on the approach to the station.
Fishermen were interviewed to determine distance traveled, gender, license
type, total hours fished, fishing method, bait, shore or boat, number of fish
caught, and number of fish released. Lengths, weights, and scales were taken
of the fish which had not been dressed. In 1975 the station was operated on
subsequent days during the week (i.e. Monday one week, Tuesday the next week,
etc.), and alternate weekend days. The 1976 fishing season was stratified by
two week periods, with two weekdays and two weekend days randomly selected for
each period. Data were recorded on creel census forms and transferred to com-
puter cards for analysis.
t
LIMNOLOGY
The drawdown of Tongue River Reservoir in anticipation of repairs to the
discharge tunnel which were scheduled for the fall of·1g75 wa~ begun in July
1975. Storage in the reservoir reacheg a minimum of 16.15 hm (13,100 af) on
September 30 and increased to 23.99 hm (19,460 af) on November 1 when repairs
began (figure 30). Discharge was maintained at approximately 0.57 m3/sec (20
cfs) for the month of November while repairs were made. Due to reduced dis-
charges, reservoir storage increased to 43.40 hm3 (35,200 af) on December 31.
The reservoir stage remained constant throughout the winter, increasing to a
peak of 73.72 hm3 (59,790 af) on June 30. Discharge was regulated in response
to increased downstream demands in late summer, when it exceeded inflow, but
was diminished in the fall relative to the inflow to increase storage to about
43.16 hm3 (35,000 af) for the winter months.
The Tongue River Reservoir can be characterized as a bicarbonate water with
calcium as its dominant cation (Whalen et al. 1976). Other abundant ions are
S04, Mg, and Na. Winter 02 sampling suggested a low potential for winter fish
kill in the reservoir since 02 did not fall below 10mg/1 during ice cover. Win-
ter fish kill potential for cool-water fish does not become critical until 02 con-
centrations fall below 5 mg/1. Even with increased organic production, little
winter kill would probably result because of the short retention time of there-
servoir. It was determined that the mine discharge water is altered ground water.
The major alteration is an increase in conductivity as a result of increased Ca,
HC03, Mg, and S04. Mine water flow was never greater than 0.47 percent of the
Tongue River flow and thus had a negligible effect on the river because of dilu-
tion.
Van Voast and Hedges (1975) pred~ct that, with three mines in operation,
mine effluent will increase to 0.17 m /sec (6.0 cfs). Assuming this flow level
under hypothetical flow and chemistry conditions, Whalen and Leath (1976) pre-
dicted little change in river quality.
FISH POPULATIONS
HISTORY
The Tongue River Reservoir and a portion of the drainage upstream were chem-
ically treated in 1957 to remove undesirable fish species. Following rehabilit-
ation, the reservoir was stocked with rainbow trout in an attempt to duplicate
fishing which commonly follows the initial impounding of reservoirs. Over two
million fingerling rainbow trout were planted during the years 1958-1960. Gill
net sampling in November 1959 produced 80 rainbow per net night; sampling in 1960
took only seven rainbow per net night. Stocking with trout was stopped because
the undesirable fish species had again built up to high population levels. How-
ever, correspondence in 1962 suggests that the reservoir was still producing some
85
35
30
.25
~
<.>
CD .. .........
E 20
CD
Cl'
~
0
~
0 .. 15
0
())
"'
10
5
F
I
j
:t
:J
J
J :,
:t :t
J
.~
. 'I
I
A M
• A
f~
t~ 1: 1: . ,.
1: 1:
I• •
: I : I• • • I .
I: I:
I: I: I; .
I •
I •
J A
,1975
s 0 N 0
--Storage
---Inflow
•• • • ••• Outflow
0
1976
Figure 30. Inflow and outflow of Tongue River at Tongue River Reservoir compared with
storage elevation of the reservoir from April 1975 to October 1976.
---
80
70
60
50 ,;;-
E
s::; -
40 .,
"' 0
~
0 -(/)
30
20
10
good catches of rainbow trout, with fish ranging from .7 to 2.7 kg (1~ to 6
lb) being harvested by anglers.
Stocking recommendations for a warm-water fishery in the reservoir were
implemented in 1963 and are summarized in table 22. Northern pike fry and
fingerling were stocked from 1963 through 1966 to develop a self-sustaining
population. Northerns were not planted in 1967 and 1968, as a check on natural
reproduction, but were again planted in 1969. Fingerlings, rather than fry,
were planted from 1972 to 1976 to evaluate the effects of different numbers and
sizes of fish. Channel catfish were introduced in 1963 and 1964, and largemouth
bass were planted in 1964 and again in 1972 and 1973. Walleye were stocked from
1965 to 1969. Since the first plant of walleyes would have matured in 1970, this
plant was discontinued as a check on spawning success.
SAMPLING RESULTS
Fish were collected for analysis using the methods explained on page 83.
Results of frame trap net catches are tabulated by month and reservoir zone for
each species collected in tables 23 (1975 collections) and 24 (1976 collections).
As shown in table 25, the number of fish taken per net night with trap nets has
·increased since 1g12. Catch rates per net night were similar from 1972 through
1974 but more than doubled from 1974 to 1975 and from 1975 to 1976. Fewer traps
were fished in 1976, and efforts were concentrated on catching mature northern
pike for an egg viability study.
Gill nets are utilized to follow fish population trends. Eighteen experi-
mental gill nets were fished on .the bottom for a 24-hour period each year. Gill
net catches for the years 1964 through 1976 are summarized in table 26. Table
27 shows average lengths and weights, as well as number caught per net, for all
species collected in overnight gill net sets.
Northern Pike
Habitat Preference. Marshes and warm, weedy bays constitute the preferred
spawning habitats of northern pike (Esoz lucius) in lakes and reservoirs. Spawn-
ing occurs in the early spring, immediately after the ice melts. Mature adults
move into shallow, vegetated marshes andbays for spawning, scattering their eggs
over the vegetation: The physical characteristics and water level management of
the Tongue River Reservoir has resulted in a limited amount of good northern hab-.
it~t. Marshes are present only during maximum storage; weedy bays are almost
nonexistent. Natural reproduction has not been documented in the reservoir.
Catch Rates and Distribution. Frame trap nets fished during the spawning
season in 1975 and 1976 caught a total of 176 and 132 northern pike, respect-
ively (tables 23 and 24). In 1975, 29.5 percent (52 of 176) of the northerns
were recaptured one or more times; in 1976, 35.6 percent (47 of 132) of the sam-
ple were recaptured fish.
Northern pike were taken almost exclusively in zone A in 1975 (91.5 percent
of the total northern catch); in 1976 the catch was distributed between zones
A (62.1 percent) and B (37.9 percent). Zone A represents the best northern hab-
itat in the reservoir. In 1975, the greatest northern catch (55.1 percent) oc-
curred in May. In 1976, most northerns (59.1 percent) were captured in April.
Spring ice melt was late in 1975 (about April 24) as compared to 1976 (April 9),
which accounts for the greater April catch rates in 1976.
87
TABLE 22. Summary of warm-water fish plants in the Tongue River Reservoir,
1963-75.
Year Species Size Number
1963 Northern pike Fry 210,000
Northern pike Fingerling 35,200
Channe 1 catfish 3-inch 20,608
1964 Northern pike Fry 100,000
Channel catfish 2-inch 99,180
Largemouth bass l-inch 150,000
1965 Northern pike Fry 339,300
Walleye Fry 750,000
1966 Northern pike Fry 210,500
~Ia lleye Fry 100,000
1967 Walleye Fry lg7,750
1968 Wall eye Fry 601,214
1969 Northern pike Fry 650,000
Northern pike Fingerling 513,200
Walleye Fry 92,480
1970 Northern pike Fry 1,125,000
1971 Northern pike Fry 360,000
1972 Northern pike Fingerling 14,058
Largemouth bass 2-inch 199,290
1973 Northern pike Fingerling 13,184
Largemouth bass 2-inch 27,540
1974 Northern pike Fingerling 3,330
1975 Northern pike Fingerling 32 '775
1976 Northern pike Fingerling 50,000
88
CD
\0
TABLE 23. Summary of trap net catches by zone in the Tongue River Reservoir, 1975
April May June
A B c A B c A B
Northern pike 67 I I 89 6 2 5 4
Carp 195 23 27 264 53 34 10 8
Goldfish 21 I II I I 8
Golden shiner 17 I I 15 60 8 8 104
Shorthead redhorse 2 9 5 5 3 4
White sucker 5 2 I 5 8 2 36
Longnose sucker 0
Black bullhead 11 1 13 20 4 1 1
Yellow bullhead 2 2 33 10 1 6
Channel catfish 0
Stoneca t 0 3 2
largemouth bass 0
Smallmouth bass 9 1 1
Rock bass 1 7
Green sunfish 2 1 2 2
Black crappie 34 2 62 125 97 31 77
White crappie 83 2 211 717 89 577 3850
Sauger 2 3 11 2 3 1
Walleye 26 31 9 8 3 7 3 15
Yellow perch 75 11 9 83 542 2 I
TOTAL 542 73 43 707 1132 811 647 4198
NET NIGHTS 20 5 3 41 33 23 13 38
FISH PER NET NIGHT 27.1 14.6 14.3 17.2 34.3 35.3 49.7 110.5
Tota 1
c A B c Tota 1
I 161 11 4 176
3 469 164 64 697
33 9 I 43
8 40 165 17 222
2 14 9 7 30
53 8 41 63 112
I 1 1
3 25 22 7 54
2 5 39 12 56
5 5
1 10 2 12
1 1 7 8
3 2 3 8
374 127 202 473 802
372 871 4569 461 5901
16 4 2 22
37 49 16 102
17 86 95 559 740
838 1896 5403 1693 8991
21 74 76 47 197
39.9 25.6 71.1 36.0 45.6
1.0
0
TABLE 24. Summary of trap net catches by zone in the Tongue River Reservoir, 1976.
April May June
A B c A B c A B
Northern pike 50 28 32 22
Carp 19 5 2 2 I
Goldfish 8 I 3
Golden shiner 57 97 76
Shorthead redhorse I I 2 2
White sucker 2 3
Longnose sucker
Black bullhead 29 30 12
Yellow bullhead 4 71 18
Channel catfish 0
Stonecat 4 1
Largemouth bass 0
Smallmouth bass 2 2 7 3
Rock bass 2 3 4
Green sunfish 2 I
Black crappie 120 20 0 119 181 141
White crappie 776 6 0 1840 2312 127 42
Sauger 34 I 2 9 4 6
Walleye 7 2 3 10 6
Yellow perch 73 1 35 17
TOTAL 1190 64 5 2260 2667 283 42
NET NIGHTS 12 7 I 13 15 8 1
FISH PER NET NIGHT 99.2 9.1 5.0 173.8 177.8 35.4 42.0
Total
c A B c Total
82 50 0 132
21 7 I 29
9 3 0 12
!54 76 0 230
I 3 2 6
2 0 3 5
0 0 0 0
67 12 79
75 18 93
0
4 1 5
0 0 0 0
4 7 3 14
5 4 9
3 0 0 3
7 239 201 148 588
6 2616 2360 133 5109
43 5 6 54
17 8 2 27
108 18 3 129
13 3450 2773 301 6524
3 25 23 12 60
4.3 138.0 120.6 25.1 108.7
TABLE 25. Comparison of trap net catches: Tongue River Reservoir, 1972-76 (expressed as numbers per net night).
1972 1973 1974 1975 1976
No. ,; tlo. % No. % No. ,; No. %
Northern pike 0.34 I. 78 0.25 I. 79 0.95 5.79 0.90 1.97 2.20 2.02
Carp 7.05 37.10 3.39 24.40 1.46 8.90 3.49 7.63 0.48 0.44
Goldfish 0.01 0.05 0.02 -0.14 0.10 0.61 0.22 0.48 0.20 0.18
Golden shiner 0.09 0.47 0.11 0.79 0.04 0.24 1.24 2. 71 3.80 3.50
Shorthead red horse 0.13 0.68 0.21 I. 51 0.29 1.77 0.16 0.35 0.10 0.10
White sucker 0.19 1.00 0.49 3.52 0.30 1.83 0.57. 1.25 0.08 0.07
Longnose sucker 0.03 0.21 0.03 0.18 0.01 0.02
Black bullhead 1. 51 7.94 0.43 3.09 0.55 3.35 0.27 0.86 1.32 I. 21
Yellow bullhead 0.26 1.59 0.28 0.61 1.55 1.43
Stone cat 0.01 0.07 0.01 0.06 0.03 0.06 0.08 0.07
Largemouth bass 0.01 0.05 0.02 0.12
Smallmouth bass 0.01 0.05 0.01 0.07 0.03 0.08 0.06 0.13 0.23 0.21
Rock bass 0.01 0.07 0.01 0.06 0.04 0.08 0.15 0.14
Green sunfish 0.02 0.14 0.02 0.12 0.04 0.08 0.05 0.05
Black crappie 1.24 6.52 1.30 9.35 2.99 18.24 4.08 8.92 9.80 9.02
White crappie 1.99 10.47 3.50 25.19 7.96 48.55 29.95 65.50 85.15 78.34
Sauger 0.02 0.14 0.09 0.55 0.09 0.20 0.90 0.83
walleye 0.38 2.00· 0.12 0.86 0.33 2.01 0.47 1.03 0.45 0.41
Yellow perch 6.05 31.84 3.96 28.56 0.96 5.85 3.83 8.34 2.15 1.98
TOTAL 19.00 13.89 16.40 45.73 108.69
NO. NET NIGHTS 85 121 168 197 60
TABLE 26. Su11111a ry of gill net (bottom) sets in the Tongue River Reservoir, 1964-76, expressed as numbers of fish
per net set.
1964 1966 1968 1969 1970 1971 1972 1973 1974 1975 1976
Brown trout 0.1
Rainbo>l trout 0.1 0.1
Northern pike 0.8 0.8 0.1 0.2 0.3 0.2 0.2 1.2 0.6 0.1 0.2
Carp 4.2 2.5 4.6 8.4 6.3 4.1 4.6 6.9 3.3 4.8 3.9
Golden shiner 12.0 0.3 0.7 0.6 0.1 0.2 0.1
Goldfish 0.1 0.2 0.1 0.1 0. 1
Longnose sucker 0.5 0.3 0.1 0.2 0.1 0.1
Shorthead redhorse 0.8 9.0 1.2 6.5 3.5 1.7 10.2 21.5 10.3 11.2 8.6
White sucker 16.8 3.8 5.0 1.3 2.9 0.6 3.3 4.7 1.9 2.2 4.1
Black bullhead 15.2 12.0 4.2 2.8 1.4 0.7 3.7 5.0 0.7 0.3
Yellow bullhead 2.7 6.4 3.2
Channel catfish 0 .I 0.1
<0 Stonecat 0.1 0.1 N
Largemouth bass 0.5 0.1
Smallmouth bass 0.1 0.3 0.3 1.0 1.9
Pumkinseed 0.2 0.1
Rock bass 0.2 0.2 0.1
Black crappie 3.1 0.3 0.3 0.6 0.2
White crappiea 22.5 9.8 16.8 15.8 9.2 11.3 7.2 11.9 16.4 14.7 25.8
Sauger 0.6 1.0 1.4 1.0
Wall eye pike 0.7 0.1 0.7 0.5 0.4 1.5 2.5 1.7 2.8 1.9
Yellow perch 1.5 10.0 4.0 7.7 4.1 8.4 5.6 4.3 1.7 1.2
TOTAL 74.8 48.2 36.9 44.4 28.4 27.6 39.9 59.7 40.8 47.9 52.6
NUMBER OF SETS 4 6 18 18 18 18 18 18 18 18 18
alncludes black and white crappie, 1964-71.
,
Numbers of northerns taken by gill net during the summer sampling period
declined from 1.2 fish/net in 1973 to 0.1 fish/net in 1975, increasing slightly
to 0.2 fish/net in 1976 (table 27).
TABLE 27. Catch statistics of 18 overnight gill net (bottom) sets, Tongue
River Reservoir, July 1975 and 1976.
No./Net
Species No. Set
Brown trout
Rainbow trout 1 0.1
Northern pike 2 0.1
Carp 87 4.8
Golden shiner 1 0.1
Longnose sucker 1 0.1
Shorthead redhorse 202 11.2
White sucker 40 2.2
Channel catfish 1 0.1
Black bullhead 13 0.7
Yellow bullhead 116 6.4
Stonecat 1 0.1
Largemouth bass 1 0.1
Smallmouth bass 18 1.0
Rock bass 2 0.1
Green sunfish
Pumpkinseed 1 0.1
Black crappie 10 0.6
White crappie 265 14.7
Sauger 18 1.0
Wall eye pike 51 2.9
Yell ow perch 30 1.7
TOTAL 862 47.9
CONVERSIONS: 1 mm = .0394 in
1 g = .0022 lb
1975
Average
Length
(mm)
185
515
410
81
237
322
2g9
356
227
219
210
147
269
168
126
119
198
510
398
165
1976
Average Average
Weight No. /Net Length
(r~) flo. Set (mm)
1 0.1 287
140
865 3 0.2 661
837 70 3.9 429
40
110
363 155 8.6 331
464 73 4.1 377
360
203 5 0.3 211
152 58 3.2 223
100 2 0.1 175
40
285 34 1.9 217
178 1 0.1 110
3 0.2 111
40
53 3 0.2 221
128 465 25.8 206
553 18 1.0 405
772 34 1.9 430
50 21 1.2 169
946 52.6
Average
Height
(g)
220
1470
978
464
641
142
174
90
168
10
23
123
121
659
869
65
Young-of-the-year northerns were taken by electrofishing coincidentally with
smallmouth bass sampling in 1976. By September the young northerns had attained
a length of 298 mm (11.7 in). l~hile it was not possible to estimate survival of
the 1976 spring plant, subsequent recapture of marked fish suggests a good surviv-
al rate and the possibilities of good year-class strength.
93
Size A~e 1 and Growth. Northerns ranged in length from 3g4 to 1,156 mm
(15.5 to 45. 1n) in 1974, 282 to 1,301 mm (11.1 to 51.2 in) in 1975 and 571
to 1,165 mm (22.5 to 45.9 in) in 1976 (table 28). Average lengths were 719,
808, and 802 mm (28.3, 31.8, and 31.6 in), respectively, while the average
weight increased from 2,937 g (6.46 lb) in 1974 to 3,236 g (7.12 lb) in 1976.
The length-frequency distribution of northerns caught in the traps reveals
distinct age groups in the spawning population (figure 31). The fingerlings
planted in 1972 entered the spawning population in 1974 at a length interval
of 450-650 mm (18 to 26 in). This age class increased to a length interval of
500-700 mm (20 to 28 in) in 1975 and 700-850 mm (28 to 33.5 in) in 1976. The
reduction in the number of northerns planted in 1973 and 1974 is shown by lack
of distinct age groups entering the spawning population in 1975 and 1976. The
absence of these age groups further suggests limited natural reproduction in
the reservoir.
TABLE 28. Average lengths and weights of northern pike caught in trap nets in
the Tongue River Reservoir, 1972-76.
Year
1972
1973
1974
1975
1976
Average
Length
No. a (rrm)
29 747
48 732
140 719
136 808
133 802
CONVERSIONS: 1 mm = .0394 in
1 g = .0022 lb
aooes not include recaptures.
Average
Range Weiyht (mm) (g
597-1,080 3,746
648-1,189 3,750
394-1,156 2,937
282-1,301 3,083
571-1,165 3,236
The average length of northern pike taken in gill nets for the years 1964-
1976 shows wide variation (figure 32). The increase in length from 1964 to 1969
represents maturity of early plants. The reduction in 1970 followed by an in-
crease reflects the discontinuance of stocking followed by stocking resumption.
A small sample of scales (17) taken from trap-netted pikes 1-1ere analyzed
for age class sizes. Three age classes (II -IV) were represented, and the
me~n lenqth for each age class was 218 mm (four fish), 523 mm (nine) and 773 mm
(four), respectively. These are within the ranges reported for other northern __
pike populations (Scott and Crossman 1973). lhe mean length of age group IV
(773) corresponds closely with the mean of the 1972 age 0 class, as shown in
the length-frequency distribution (figure 32).
Population Estimates. Population estimates were computed for northern pike
based on the modified Schnabel estimator using trap-netted fish. Estimates of
northern pike population greater than 275 mm were 272 in 1974, 228 in 1975, and
138 in 1976 (table 29). Confidence intervals at the 95 percent level showed a
94
.JI:. u -c
(.) -0
CD
"' c -c
CD u
~
CD
D..
25
20
15
10
5
400
I
I
l
500
I
I~
I I
I I
I I
I I
1 I
I I
I I
I
. I
: I :I
t
I :.
I
I
I
I
I
I
I
600
·.
'I :I
\
I
\
:\
':\
:1 ·. \
: \
: ' .. ·· ••
:'1
I ."1
I ."1
~:I ,.,1
: \ .·
: \ .·· : .. ,
:.-. \
700 800
Length (mm)
' ' ' ,_
900
1976
----1975
1000
1974
... ·-
1100
Figure 31. Length-frequency of northern pike captured in trap nets,
Tongue River Reservoir, 1974-76, expressed as each size interval's percentage
of the total sample.
significant decrease from 1975 to 1976. This reduction appeared to be in larg-
er fish, as shown in figure 31. Based on the average weight of trap-netted
fish, the northern pike standing crop was estimated at 0.564 kg/ha (.503 lb/
acre) in 1974, 0.496 kg/ha (.442 lb/acre) in 1975, and 0.315 kg/ha (.281 lb/
acre) in 1976. The standing crop of northerns in the Tongue River Reservoir
is considerably lower than most others reported. For example, estimates of
standing crops of northern pike in Wisconsin lakes ranged upward from 0.673 kg/ha
(Snow and Beard 1972); in a southern Michigan lake, crops ranged from 3.5 to
5.3 kg/ha (Schneider 1971). Scott and Crossman (1973) reported standing crops
95
1100
1000
900
e Average Length
Range
~ 800 E
E
~
;: 700 "' t c .,
_J
600
500 •
400 • +
300
1964 66 68 69 70 71 72 73 74 75 76
Figure 32. Average length and length range of northern pike from
gill-net catches, Tongue River Reservoir, 1964-76.
of northern pike from various habitats across North America generally range
between 1.5 and 4.6 kg/ha. The low population levels shown in this reservoir
are probably the result of poor habitat quality and the lack of natural repro-
duction.
TABLE 29. Population estimates of northern pike determined from trap net
catches, Tongue River Reservoir, 1974-76.
Number Number Population Confidence
Year Examined Recaptured Estimate Interva 1 sa
1974 169 36 272
1975 1BO 52 228 218-238
1g76 85 48 138 116-172
aconfidence interval not computed for northern pike in 1974 due to variation
in recapture distribution.
. 96
[
30).
cent
year
lar
Tagging. Tags have been placed in 274 adult northerns since 1973 (table
Angler returns have been consistent, with an average return of 13.9 per-
(range 12.5-16.4 percent). The highest return rate occurred the same
the fish were tagged. An overall return rate of about 14 percent is simi-
to catch rates reported for other marginal northern pike waters.
TABLE 30. Summary of northern pike tag returns by year for Tongue River Reser-
voir,1973-76. (Number in parentheses is the percentage of total tagging)
Year Number Tao Returns bv Year
Tagged Tagged 1973 1974 1975 1976 Total
1973 41 5 (12.2) 1 (2.4) 6 (14.6)
1974 110 8 (7.2) 6 ~ 5. 5) 2 ( 1.8) 16 (14.5)
1975 73 7 9.6) 5 (6.8) 12 (16.4)
1976 50 4 (12.5) 4 (12.5)
TOTAL 274 38 (13. 9)
Walleye and Sauger
Habitat Preference. Sauger (Stizostedion canadense) and walleye (Stizo-
stedion vitreum) are tolerant of a great range of environmental situations,
with both preferring large, shallow lakes. Sauger are also found in tur-
bid, slow-flowing rivers. Sauger generally succeed over walleyes in very tur-
bid waters. Both species are generally absent from vegetated waters. Spawning
occurs in the spring, with both species moving either upstream or to suitable
rocky areas. Eggs are deposited at random among the rocks to incubate.
The Tongue River Reservoir provides good walleye and sauger habitat, and
both populations are doing well. Walleyes were introduced from 1965-1969 and
are now successfully reproducing. Sauger were not taken in the reservoir until
1973. Personal communication with Wyoming Game and Fish personnel revealed that
sauger were transplanted into the Tongue River near the Wyoming-Montana state
line in about 1967. The fish apparently moved into the reservoir and have become
an established population.
. Catch Rates and Distribution. In 1975, the trap-net catch of walleyes was
distributed about equally between zones A and B, which contribute 40.7 and 41.7
percent, respectively; in 1976, 63.0 percent of the walleyes were taken in zone
A, and 29.6 percent in zone B (tables 23 and 24). These zones represent the
best walleye habitat. Ho~tever, the effort to obtain mature northern pike in
1976 precluded equal sampling effort, and the results may not represent the true
species distribution in the reservoir. In 1975, the walleye catch was largest
in April; in 1976 the catch was about equally distributed between April and May.
Catch rates were consistent in 1975 and 1976 (table 25).
Sauger were absent from trap-net catches until 1973, when they contributed
0.02 fish per net night (table 25). Catch rates in 1974 and 1975 were 0.09, in-
creasing to 0.90 in 1976. In 1975 and 1976, sauger were taken primarily in zone
A (72.7 to 79.6 percent of sauger catch, respectively). This zone is generally
turbid during the spring season and probably represents preferred sauger habitat.
97
The catch per gill-net set for walleye ranged from 0.1 to 0.7 from 1966
to 1969, increasing to 1.5 in 1972 and 2.5 in 1973. The highest catch was in
1975, 2.8 fish per net. Walleye increased in size from 1966 to 1971, then
stabilized from 1972 to 1976 at a level just below the 1969-70 averages (figure
33). Sauger were not taken in gill nets until 1973, when 0.6 fish per set were
taken, as compared to 1.4 and 1.0 fish per set taken in 1975 and 1976, respect-
ively. Sauger appear to be increasing and are showing up in angler's creels .
800 • Average Length
Range
700
600
~ E
E 500 -
~ -t 0
c:: 400 .,
..J •
300
200
100
1966 68 69 70 71 72 73 74 75 76
Figure 33. Average length and length range of walleyes from gill-
net catches, Tongue River Reservoir, 1966-76.
~ize, Age, and Growth. The average length of trap-netted walleye has varied
only about 13 percent since 1972, although the average weight has varied by
25 percent (table 31). The presence of small f1sh 1n the sample 1ndicates
walleyes are successfully spawning in the reservoir.
Length-frequency distributions for walleye (1974-76) are shown 1n figure
34. The size interval of 575-624 mm was dominant in 1974, contributing 31.1
percent. In 1975, young fish with a peak length of 350 mm (300-400 mm) were
dominant, comprising 43.9 percent. This s1ze group sh1fted 100 mm in 1976, with
a peak of 450 mm (range 400-600 mm). Small fish were absent in 1976, suggesting
a weak year class entering the populat1on. Scale samples taken during the
spawning season suggest that walleyes enter the run at age IV+. Reservoir
storage showed a poor pattern in 1972; maximum stage was reached during March,
and water levels dropped during April with a slight increase during May. Thus,
98
r
TABLE 31. Average lengths and weights of walleye caught in trap nets in the
Tongue River Reservoir, 1972-76.
Year
1972
1973
1974
1975
1976
.c u -D
(.) -0 .,
"' D -c .,
u
~ .,
D..
Average Average
Length Range weirht No.a (nun) (nun) (g
32 495 359-569 1,335
24 541 353-645 1,643
44 511 305-799 1,507
90 470 269-813 1,217
27 538 434-727 1,629
CONVERSIONS: 1 nun = .0394 in.
I g = .0022 lb.
aooes not include recaptures.
50
40
30
20
10
200 300
...
I '\
I : '
:· .. .. : . . . . . . .
--:-' I : ' ·. \ I : '\
400
·. \ I _.·
. ' I . \ . . \ · .. ,, .
. . ..
500
Length (mm)
600 700
1976
1975
1974
800
Figure 34. Length frequency of walleyes captured in trap nets,
Tongue River Reservoir, 1974-76, expressed as each size interval's
percentage of the total sample.
99
it is possible that the lowering of the water level in 1g72 reduced the spawning
success in 1976.
The average size of sauger taken in 1976 increased from 1975 levels of 324
mm and 464 g to 404 mm and 659 g.
Tagging. Since 1973, 244 walleye and 302 sauger have been tagged in the
reservoir (table 32). Total angler returns of walleyes since then have been
5.3 percent (13 of 244), while sauger returns have been 2.0 percent (6 of 302).
Almost 80 percent of the sauger were tagged in 1976, so the number returned
should increase. Several returns have been reported with the numbered portion
of the tag absent, and only the anchor remaining in the fish. If the incidence
of this type of tag loss is high, the reported rate of return would be less
than it should he since many tags would not be noticed and others would simply
be discarded by the angler. However, the low rate of return suggests a harvest
well within tolerance limits of the fisn populations.
TABLE 32. Summary of walleye and sauger tagging and returns, Tongue River
Reservoir, 1973-76. (Number in parentheses is the percentage of total tagging)
Year Tagged No. Tagged 1973 1974 1975 1976 Total
WALLEYE
1973 10 0
1974 34 3 (8.8) 3 (8.8)
1975 129 3 (2.3) 6 (4.7) 9 (7.0)
1976 71 1 (1.4) 1 (1.4)
TOTAL 244 13 (5.3)
SAUGER
1974 11 0
1975 59 2 (3.4) 2 (3.4) 4 (6.8)
1976 232 2 (0.9) 2 (0.9)
TOT~L 302 6 (2.0)
Crappie
Both black (Pomoxis nigPomaculatus) and white (Pomoxis annuZaPis) crappie
are found in the Tongue River Reservoir. Stocking records, dating to 1950, do
not show introductions of crappies into the reservoir. Both species were pre---
sent when the fish population was chemically removed in 1957. This panfish is
the most abundant sport fish in the Tongue River·Reservoir and is a popular
target of anglers.
Catch Rates and Distribution. White crappie were the dominant fish in
trap-net catches in 1974, 1975, and 1976 (tables 23 and 24), making up 48.6,
65.5, and 78.3 percent of the total catch, .respectively. Black crappie were
taken in the catch, but were less significant, contributing 18.2, 8.9, and
100 1
9.0 percent in those years. Catch rates for white crappie have increased from
1.99 fish per .trap night in 1972 to 85.15 fish per trap night in 1976 (table
25). Black crappie have also increased since 1972, but not as dramatically.
In 1975, both species were taken in greatest numbers during June, with 81.3 per-
cent of the whites and 60.1 percent of the blacks taken that month. In 1976,
83.7 percent of the whites and 75.0 percent of the blacks were caught during
May.
White crappie were the predominant species in gill-net catches in 1975
and 1976 (table 27). Blacks were represented in the gill nets at about the
same levels as in trap nets (table 25). White crappie sample size almost
doubled from 1975 to 1976 (265 to 465), resulting in a corresponding increase
in the spring population estimate. The average size of white crappie was simi-
lar in 1975 and 1976.
Crappie exhibited a differential distribution pattern in the reservoir.
In 1975, 59 percent of the blacks were taken in zone C, ~1hile only 7.8 percent
of the whites were captured in that zone. Zone B produced the majority of the
white crappie in 1975 (77.4 percent). The 1976 results are masked somewhat,
since traps were not fished in zone C equally as in zones A and B. Still,
white crappie were found almost exclusively in zones A and B (97.4 percent),
while blacks were distributed more evenly; Zone C produced 25.2 percent of the
blacks. Catch rates in zones. A, B, and C in 1976 for white crappie were 104.6,
102.6, and 11.1 fish per net night respectively, as compared to 9.6, 8.7, and
12.3 fish per net night, respectively, for black crappie. The distribution
pattern probably reflects a difference in water quality between the upper (zone
A) and lower (zone C) ends of the reservoir. The difference in distribution
reflects the habitat preferences of each species, with blacks preferring clearer
water (Brown 1971).
Size, ·Age, and Growth. Length-frequency distribution for black and white
crappie for 1975 and 1976 trap-net catches is shown in figure 35. Black crappie
show a greater distribution of lengths, ranging from under 100 to 499 mm (3.9
to 19.6 in), while white crappie ranged from 100 to 399 mm (3.9 to 15.7 in).
Black crappie produce larger fish, with specimens to 1,362 g (3 lb) common. In
both years, the modal size for whites was 225 mm (8.9 in), compared with 250 mm
(9.8 in) for blacks.
Scales taken during the spring (April-May) 1975 trap net season from black
and white crappie were analyzed for age and growth. A summary of 1 engths and
masses is shown in table 33. The oldest white crappie taken were of age group
X; the oldest black crappie were of age group VIII. White crappie grew faster
until age V, at which time the blacks took over. By weight, blacks caught up
with whites at age IV. A comparison of lengths of fish taken in June and July
shows a faster ~rowth rate for blacks than whites. Comparing the age data with
figure 35, age III fish contribute the greatest percentage of the spawning pop-
ulation. A comparison of age data on black and white crappie with data from
other northern waters (Nelson 1974, Scott and Crossman 1973) shows that the
fish in the Tonque River Reservoir grow at similar rates.
Population Estimates. Population strengths of black and white crappie
were estimated in 1975 and 1976 (table 34). The total crappie estimate in
1g75 was 46,613 fish, ~lith whites contributing 94.6 percent of the total.
The population increased in 1976, with a total estimate of 95,684 crappie
101
50
40
.c u -0 30 <.J -0
CD
"' 0 -c
CD u
~ 20 ..
Q.
0
"'
10
0
0 100
~ 1\
I I
I \
I I
I I
I I
I I
I I
I I I I
1 I
I I
I I
I I
I I
' ' I I
I I
I I
I
I
I
--
200 300
Length (mm)
White Crappie
50
40
30
400 500 0 100 200 300
Length (mm)
Black Crappie
1976
----1975
400 500
Figure 35. Length-frequency distribution of white and black crappie taken in trap nets,
Tongue River Reservoir, 1975-76, expressed as each size interval's percentage of the total sample.
,
TABLE 33. Average lengths and weights of black and white crappie, Tongue
River Reservoir, April-May 1975.
White Crappie Black Crappie
Average Average Average Average
Age
II
I I I
IV v
VI
VII
VI II
IX
X
No.
Length
(nun)
Wei~ht (g
3 173 50
10 219 174
30 245 222
16 262 277
13 280 349
2 286 415
1 382 318
1 423 1160
2 363 887
Conversions: 1 mm = .0394 in
1 g = .0022 lb
No.
Length
(mm) Wei~ht
(g
7 137 34
21 195 111
23 237 222
20 272 345
13 311 537 g 361 781
5 396 1090
(90.8 percent whites). Estimates of standing crop for white crappie in 1975
and 1976 were 6.2 kg/ha (5.5 lb/acre) and 12.3 kg/ha (11.0 lb/acre), respec~
tively,and 0.535 kg/ha (.478 lb/acre) and 1.9 kg/ha (1.7 lb/acre), respective-
ly, for black crappie. The estimated crappie population doubled from 1975 to
1976. Bennett (1954) reported that a late summer drawdown similar to the lowering
of the reservoir in 1975 may benefit piscivorous fishes. Small fishes and aquatic
invertebrates are forced out of vegetation. The dislocation of these animals makes
them more easily hunted by the larger fishes. Since crappie do feed heavily on
other fishes, it is possible that their overwinter survival was enhanced by the
fa 11 drawdown.
TABLE 34. Population estimates of black and white crappie determined from trap
net catches Tongue River Reservoir 1974-76 • z .
Number Number Population Estimate Confidence
Year Examined Recaptured Total Number Number/ha Interval sa
Black crappie 1975 861 117 2,526 1.8 2,458 -2,598
1976 574 18 8,792 6.2 5,937 -16,935
White crappie 1975 5,817 348 44,087 31.1 43,389 -44,808
1976 4,096 146 86,892 61.4
CONVERSIONS: number/ha = 2.47 number/acre
aconfidence interval not computed for white crappie in 1976 due to varia-
tion in recapture distribution.
Tagging. Large black and white crappie (91 blacks and q whites) taken
during the trap-net season have been tagged to evaluate movements and fisher-
man harvest. Angler returns of blacks averaged only 3.3 percent (3 of 91) over
the three-year period, and none of the tagged whites were returned by fishermen.
In 1975 and 1976, of 36 blacks and 3 whites of taggable size taken in trap nets,
41.7 percent( 15) of the b 1 acks and 66.7 percent ( 2) of the whites were recaptures
103
of previously tagged fish. The low angler return and high return to traps
suggests that the population of large crappie is small.
Bass
Largemouth bass (Miaropterus sabnoidesJ were introduced into the reser-
voir in 1964 and again in 1972-73, but are rarely taken by fishermen .. While
smallmouth bass (Miarovterus dolomieuiJ have never been stocked in the reser-
voir, they are reproducing and beginning to play an important part in the
angler's harvest. Correspondence from the Wyoming Game and Fish Department
(Mueller 1973) indicates that smallmouth bass were stocked in a strip-mine
pond near Sheridan and that high spring flows from the Tongue River washed into
the ponds, introducing smallmouth into the river and subsequently into the
reservoir.
Catch Rates and Distribution. Catches of smallmouth bass have been small
in trap nets, ranging from 0.01 fish per net night in 1972 and 1973 to 0.06
fish per net night in 1975 (table 25). In 1976, however, the catch increased
to 0.23 smallmouth per net night. Zone B produced B3.3 percent of the catch
in 1975 and 50.0 percent in 1976. The largest number of smallmouth were taken
in May both years. Largemouth bass have been nearly absent from trap-net sam-
ples.
Gill nets produced smallmouth beginning in 1972, and catch rates increased
from 0.1 fish per net in 1972 to 1.9 fish per net in 1976 (table 26). Large-
mouth have been absent from gill nets also. The average length and weight of
smallmouth taken in gill nets decreased from 251 mm to 304 g in 1975 to 217 mm
and 168 g in 1976, indicating the recruitment of young fish into the population.
A baseline index of reproductive success was established with 100-ft shore
seine and a 50-ft bag seine. Seine hauls covering approximately 15-30 m of shore
were made to obtain bass fry and juveniles. When all size groups were combined.
date from 1975-50-ft seine, the 1974-100-ft seine, and the 1975-100-ft seine
were relatively consistent. (table 35). Zone A had the fewest smallmouth and
largemouth fingerlings per 100m of shoreline; zone Chad the most (Gregory and
Penkal 1975). There were more largemouth than smallmouth fingerlings per 100m
in zones C and A and fewer in B. For all areas combined, largemouth bass,~
made up 78.0 percent of the fingerling catch and smallmouth the other 22.0 per-
cent.
Size, Age, and Growth. Penkal (1977) found that scale annuli of small-
mouth bass in the Tongue River Reservoir were formed beginning in July and
were complete by early August. The scale-length relationship was calculated
and used as a correction factor for back calculation of smallmouth bass growth
(table 36). Growth of smallmouth bass in the Tongue River Reservoir is above
average for a northern lake. Calhoun (1966) reported a range for northern lakes
of 246 mm (Michigan) to 310 mm (Minnesota) for fish at their fourth annuli.
The average length of the 1972 age 0 class in the Tongue River Reservoir was
308.3 mm. This good growth could be attributed to the smallmouth's recent
exploitation of the new habitat or to favorable environmental conditions.
The growth of 1 argemouth bass in the reservoir ~1as a 1 so i nves ti gated by
Penkal (1977). A summary of the back-calculated growth of largemouth is sho~m
104
TABLE 35. Number of bass per 100m of.shoreline, Tongue River Reservoir,
1974-75.
100-ft Seine
1974
Fry LMBb
Fry SMBb
Juvenile LMB
Juvenile SMB
All LNB 56.3
All SMB 14.0
All LMB & SMB 70.3
aGregory and Penkal 1975
bLMB = largemouth bass
SNB = smallmouth bass
50-ft Seine
1975° 1975a
36.3 39.8
14.2 18.1
1.8 0.1
11.8 11.4
38.3 39.9
26.9 30.1
65.2 70.0
TABLE 36. Back-calculated lengths (mm\ of smallmouth bass, Tongue River Reser-
voir 1976 •
Year Class No. I I I
Zone A
1971 6 97 226
1972 1 80 242
1973 7 81 170
1974 5 85 211
1975 106 76
Zone B
1970 1 84 245
1971 3 86 169
1972 3 79 177
1973 11 89 151
1974 23 86 190
1975 157 80
Zone C
1970 1 90 252
1971 2 85 194
1972 1 117 245
1973 13 88 178
1974 37 86 191
1975 55 79
SOURCE: Penkal 1977
CONVERSION: 1 mm = .0394 in
I I I
286
326
258
332
281
230
235
351
291
332
248
.
Aae Class
IV v VI
359 3B9
371
358 390 419
351 386
293
411 433 465
352 388
394
in Table 37. Largemouth bass growth also appears to be better in the Tongue
River Reservoir when compared to other studies from northern lakes. A range
of 292 mm (Kuehn 1949) to 318 mm (Bennett 1937) was reported for largemouth
bass at their fourth annuli in Minnesota and Wisconsin, respectively. In the
Tongue River Reservoir, the average calculated length of the 1972 year class
was 329 mm. It may be concluded that the habitat conditions in the Tongue
River Reservoir are favorable for bass growth.
105
TABLE 37. Back-calculated lengths (mm) of largemouth bass, Tongue River Res-
ervoir 1g75 ' .
Age Class
Year Class No. I II III IV v VI VII
1969 2 100 244 319 3B2 416 445 45g
1g7o 2 87 24g 342 385 412 442
1971 11 92 204 286 355 388
1972 5 87 203 270 329
1973 31 87 166 245
1974 65 86 1g2
1975 318 7g
WEIGHTED GRAND MEArla 81 189 264 354 395 444 459
CONVERSIONS: 1 mm = .0394 in
aweighted on basis of percentage of year class in population.
Tagging. One thousand smallmouth bass and 166 largemouth bass \~ere tagged
in the reservoir from 1g73 through 1976 (tables 38 and 39). As ~lith the other
species in the reservoir, tag return rates by anglers have been low. Smallmouth
bass averaged 1.7 percent return, while largemouth averaged 1.8 percent. The low
rate of return suggests a good population of bass not being exploited by anglers.
TABLE 38. Summary of smallmouth bass tagging and angler returns by year,
Tongue River Reservoir 1973-76 '
Tagging Returns
Year Returned Total
Year Tagged No. Tagged 1975 1976
1973 2 0
1974 3 0
1975 105 4 (3.8) 5 ~4.8l 9 (8.6)
1976 890 8 0.9 8 (0. 9)
TOTAL 1000 17 (1.7)
NOTE: Numbers in parentheses are the percentage of fish tagged in the
year indicated.
TABLE 39. Summary of largemouth bass tagging and angler returns by year,
Tongue River Reservoir 1974 76 ! -.
Tagging Returns
Year Returned Total
Year Tagged No. Tagged 1975 1976
1974 2 0
1975 15 1 1 (6. 7) 1976 149 2 (1.3) 2 ( 1. 3)
TOTAL 166 3 ( 1.8)
NOTE: Numbers in parentheses are the percentage of fish tagged in the
year indicated.
106
,
CREEL CENSUS
Using the methods explained on page 84 , 365 partie~ of anglers were in-
terviewed in 1975 and 423 in 1976 (table 40). Shore fishermen were more num-
erous than boat fishermen in 1975, contributing 53.2 percent of the total;
boat fishermen were dominant in 1976, adding 65.0 percent. Anglers expended
more time in 1976 than in 1975, and caught almost three times more fish. Ang-
lers nonresident to Montana traveling less than 50 miles made up the majority
of the fishermen (50.4 percent), followed by r1ontana residents traveling more
than 50 miles (38.7 percent).
TABLE 40. Miscellaneous statistics of Tongue River Reservoir creel census,
1975-76.
Parties interviewed
Length of trip (hrs)
Total hours fisheda
Total fish caughta
1975
365
4.42
12,522-
4,088
1976
423
6.05
20,053
11 '538
aThese are estimated figures for the entire season, all anglers.
An estimated 2,802 anglers expended 12,522 hours of fishing pressure on
the reservoir in 1975. In 1976, the pressure increased to 3,315 anglers and
20,053 hours. The estimated annual fishing pressure for the summer was 8.84
hours/ha (3.58 hours/acre) and 14.16 hours/ha (5.73 hours/acre) in 1975 and
1976, respectively. Monthly, the pressure varied in 1975 from a low of 0.28
hours/ha (.11 hours/acre) in October to a high of 1.59 hours/ha (.64 hours/
acre) in May and in 1976 from 0.45 hours/ha (.18 hour~/dcre) in October to 4.43
hours/ha (1.79 hours/acre) in June (figure 36). Fish.ing pressure fell off
during the late summer both years, increasing again with cooler temperatures
in the fall.
Pressure on the Tongue River Reservoir is less than reported on other cool
water lakes in northern latitudes. Kempinger et al· (1975) summarized fishing
pressure on other northern latitude lakes and showed a range of 42 hours(ha
(17 hours/acre) to 462 hours/ha (187 hours/acre). The low pressure estimates
on the Tongue River Reservoir suggest that it is a lightly used fishing re-
source. However, as coal development expands in the Decker area and new rec-
reation areas are developed, fishing pressure will increase. Continued efforts
must be expended to ensure that fish populations will be able to withstand
the added pressure.
Estimated angling effort and harvest rates for the sport fishery are
summarized in table 41. Crappie dominated the catch both years, contributing
66.3 and 75.3 precent in 1975 and 1976, respectively. All sport fish showed
an increased tot~l catch from 1975 to 1976. The catch rate for crappie in-
creased from 0.172 fish per hour in 1975 to 0.382 fish per hour in 1976. The
increase of crappie in the angler's creel is consistent with other sampling
conducted in 1976. Catch per hour for northern pike decreased from 1975 to
1976.
107
7000
6000
5000
"' ~
::> .. ..
"' ~ a. 4000
"' " "" .. .._
D -1976 0 .. 3000 ~ ~ 1975 ::>
0
::t:
" -0
I-
2000
1000
MAY JUNE JULY AUG SEPT OCT
Figure 36. Monthly distribution of fishing pressure, Tongue River Reservoir, 1975-76.
108
TABLE 41. Estimated total angling effort and harvest of sport fish, Tongue
River Reservoir, 1975 and 1976.
Total man-trips
Total man-hours
Total catch (number of fish)
Northern pike
Bass a
Crappieb
Walleye
Total catch {kg)
Northern pike
Bass a
Crappieb
Walleye
1975
2,802
12,522
128
604
2,149
361
3,242
202.7
151.0
516.2
337.1
1976
3,315
20,053
132
1 ,241
7,655
1, 137
10,165
205.9
310.4
1,838.2
1,061.9
Total weight (kg) 1,207.0 (0.84 kg/ha) 3,416.4 (2.41 kg/ha)
Catch success
(fish per man-hour)
Northern pike
Bass a
Crappieb
Wall eye
TOTAL CATCH SUCCESS
0.010
0.048
0.172
0.029
0.259
arncludes both smallmouth and largemouth
brncludes both black and white
0.007
0.062
0.382
0.057
0.508
Fishing success for sport fish in the reservoir averaged 0.259 fish per
hour in 1975 and 0.508 fish per hour in 1976. These catch rates are low in
comparison. to other cool-water fisheries. Reported catch rates ranged from
0.48 fish per hour (similar to the highest recorded on the Tongue) to 1.25
fish per hour (Kempinger et al .1975). The annual yield on the Tongue River
Reservoir varied from 1207.0 kg (0.84 kg/ha) in 1975 to 3416.4 kg (2.41 kg/ha)
in 1976. These figures are also lower than reported for other cool-water
lakes.
The seasonal contribution of each sport species to the 1976 total catch
is shown in figure 37. Crappie dominated the catch in May and June, falling
off throughout the remainder of the summer. Walleye began showing up in June
and peaked in July, while bass increased in July to peak in August and Septem-
ber. Northern pike contribute little to the catch. It is apparent that stock-
ing rates are not adequate to produce a good northern pike fishery in the
reservoir.
109
100
80 Others (perch, bullhead,
~
carp, suckers, ather
u nongame species) -" u Northern Pike o 60 -~ -Walleye
" .,
g 40 Crappie -c: .,
u
~ .,
Q. Bass
20
0
May June July Aug Sept
Figure 37. Monthly distribution of species as determined by creel
census, Tongue River Reservoir, 1976.
ll 0
' ' I PROJECTIONS OF FUTURE USE
In order to adequately and uniformly assess the potential effects of
water 1~ithdrawa 1 s on the many aspects of the present study, it was necessary
to make projections of specific levels of future withdrawals. The method-
ology by which this was done is explained in Report No. 1 in this series, in
which also the three projected levels of development, low, intermediate, and
high, are explained in-more detail. Summarized in appendix A, these three
future levels of development were formulated for energy, irrigation, and mun-
icipal water use. Annual water depletions associated with the future levels
of development were included in the projections. These projected depletions,
and the types of development projected, provide a basis for determining the
level of impact that would occur if these levels of development were carried
through.
IMPACTS ON THE RESERVOIR FISHERY
Through the State Water Planning Nodel (see Report No. 1 of this series),
the depleted streamflows for the Tongue River Basin which would result from
implementation of three alternative levels of energy or irrigation use were
calculated. For the low projected level of development for either type of
use, the storage capacity of the existing Tongue River Reservoir was increased
from 69,000 af to 125,000 af. The intermediate and high levels of development
required the High Tongue River Dam, which would have an active capacity of
320,000 af and would provide a firm annual yield of 134,000 af.
The impacts of development on the reservoir fishery were evaluated.
Sport fishes in the reservoir, which spavm during April and ~lay, depend on
stable or rising water levels during this period. A decreasing water level
would result in a loss of available spawning habitat and would desiccate in-
cubatina fish eaas. Stor~g~ patterns projected were judged detrimental if
they required reservoir level decreases in April and May.
For the low level of energy development, only one year out of 29 resulted
in poor reproductive potential. The intermediate level showed six years ~lith
poor spawning potential. With the high projection, storage patterns resulted
in poor reproductive potential in 10 years out of 29, an average of one year
out of three with the possibility of reduced spawning. Even 1~ith poor repro-
duction every third year, a good fishery should result from the remaining
years' reproduction.
Storage patterns associated with the three levels of irrigation develop-
ment showed no serious problems. Impacts on the fishery of the Tongue River
Reservoir would be minimal.
111
The Tongue River Reservoir is a unique fishery in an area with a low
human population. Fish population estimates, with the exception of those for
northern pike, suggest a healthy, reproducing fishery. Spawning habitat for
northerns is lacking, and present water-level management does not favor the
reproduction of this species. Stockingwithnorthern pike fingerlings has been
effective. Crappie, bass, walleye, and sauger are reproducing. The low annual
pressure estimates and catch rates indicate that this fishery's potential is
not being utilized to its fullest.
Trap-net catch rates range from 45.7 fish per net night in 1975 to 108.7
in 1976. Crappie showed .the greatest increase in number from one year to the
next. Game fish made up 3.3 percent of the 1975 sample and 3.5 percent of the
1976 sample. Population estimates computed for northern pike, black crappie,
and white crappie were comparable to those in other northern lakes. A partial
creel census conducted in 1975 and 1976 sh01'1ed a catch rate of 0.259 fish per
man hour in 1975 and0.508 fish per man hour in 1976. Harvest rates and yield
were lower than those reported for other states.
Impacts of water withdra~1als on the reservoir and its fishery are dis-
cussed. An evaluation of the dra1·1down which occurred in 1975 indicates that
it was not extremely harmful to the fishery. In fact, the crappie population
may have increased. Examination of projected reservoir levels associated with
three levels of proposed energy and agricultural development shows minimal im-
pacts on the reservoir's fishery. However, provision of ins tream flows for
fish and wildlife downstream from the dam 1~ere not considered as part of these
projections. With an increase in release for instream needs, storage patterns
could be altered. Still, as shmm by the short-term drawdown in 1975, if the
magnitude and duration of water-level reduction are not extreme, the impacts
should not be severe. An extreme drawdown for long periods of time would be
devastating.
As industrial development proceeds in this region, ~later-based recreation
provided by the Tongue River Reservoir will become increasingly important.
113
PJ Ill
by
Dennis Schwehr
115
The ·characteristics of insect and fish populations in streams are deter-
mined to a large degree by discharge and by the environmental conditions
created by discharge. The composition of the insect community, the food base
of most fish populations, is related to water velocity, a function of discharge.
To assess the impact of dewatering on fish foods and habitat, it is necessary
to determine the importance of the benthic insects to the fishes. In addition,
the maintenance of the piscivorous sport and nonsport fish populations in the
lower Yellowstone (walleye, sauger, northern pike, burbot, and channel catfish
all commonly utilize other fish for all or part of their diet) depends, in part,
on an adequate forage fish base.
PURPOSE
Fish populations, relative abundances, and food chains vary widely among
aquatic ecosystems. Each fish species is adapted to an omnivorous, herbivorous,
or carnivorous diet, but the proportions of specific foods eaten differ in each
habitat. Prey organisms that are important in one habitat may not exist in
other areas which contain the same predator species. Seasonal changes occur in
food habits of fish as relative abundances and composition of insect species
are altered during the life cycles of insects. Food habits of resident popula-
tions must be determined for individual water bodies in order to assess the
potential for impact. Impacts on fish populations are dependent on the amount
of stress placed on the food supply in a particular habitat. It is important
to establish which food species are most critical in fish diets and how
environmental change will affect the food supply.
The objectives of this investigation were: (1) to determine the foods of
selected fish species during the period of study, (2) to establish those
species' selection for preferred food items relative to their availability,
and (3) to describe the possible changes in the fish community based on
alterations in the food supply caused by potential flow reductions.
SCOPE
The efforts of this phase of research are concentrated on the food habits
of some of the major fish species of the lower Yellowstone River, primarily
shovelnose sturgeon (Seaphirhynehus platorynehus), goldeye (Hiodon alosoides),
channel catfish (Ietalurus punctatus), burbot (Lota lota), and sauger
(Stizostedion aanadense). Small numbers of northern pike (Esox luaius),
carp (Cyprinus aarpio), white sucker (Catostomus aommeraoni), smallmouth
bass (Miaropterus dolomieui), white crappie (Pomoxis annularis), walleye
(Stizoatedion vitreum), freshwater drum (Aplodinotus grunniens), and flathead
chub (Hybopaia gracilis) were collected for food analysis.
117
Broadly defined, a forage fish is any utilized by another fish as a food
source. Most fish species during their first year of life are small enough
to be utilized as food and should be considered as part of the forage base.
The availability of age 0 game and nongame species depends on their habits.
Species whose young are pelagic and typically exhibit schooling patterns
would be more susceptible to predation than those species whose young do
not normally school and commonly seek shelter among the rocks, brush piles,
or instream debris. Since the habitat requirements of most age 0 stream fishes
are poorly understood, it is not possible to determine the availability
of age 0 game and nongame fishes as forage at this time. For this study,
forage fish are defined as those species which, as adults, seldom exceed
six· inches in length. This would include all of the cyprinids and certain
others such as the stonecat and mountainsucker. These species usually remain
a food source for their entire lives.
STUDY AREA
From the mouth of the Bighorn River, the lower Yellowstone flows a
distance of 476 km (295 mi) to its confluence with the Missouri River. The
river gradient averages less than .50 m/km (2.6 ft/mi). Average flow at
Miles City in August 1975 was 460 m3/sec and 260 m3/sec in September. At
Sidney, 2jB km (154 mi) below Miles City, average discharges were 460m3/sec
and 275 m /sec during the same months.
The Yellowstone River, including the sections from the Bighorn River to
Forsyth and from Glendive to the mouth, is essentially a braided river with
numerous side channels. Only the 228 km of river from Forsyth to Glendive
can be described as meandering. Many side channels contain water only during
the spring runoff. As the water level drops in midsummer, still backwater
areas remain at the lower end of the side channels.
The morphology of the river is maintained by annual high flows. The
physical character of the river provides a variety of habitats including
shallow and deep riffles, pools, and still backwaters. This natural diversity
creates the conditions which allow the presence of a diverse aquatic community.
Forty-five of 49 fish species in the Yellowstone River are present in the
lower river, which supports a warm-water fishery (Peterman and Haddix 1975).
Twelve species are classified as game fish by the Montana Fish and Game
Department. More than 70 species of benthic macroinvertebrates are reported
for the lower river (see Report No. 5 in this series).
118
I,
FOOD HABITS ANALYSES
Food habits of fish common to the lower Yellowstone have been investigated
in other waters by a number of workers. Unfortunately, many of the studies were
conducted for lake (lentic) populations, where species composition differs
from that .of lotic waters. Also, few investigations addressed food avail-
ability, making it impossible to determine selection for specific prey
organisms. For these reasons, and because each aquatic ecosystem is unique,
many of the conclusions of other researchers cannot be applied to this study.
Most fish collected for this study were captured near Miles City or below
the Intake diversion dam. Some channel catfish were taken above the mouth of
the Tongue River. A few sauger and burbot were caught at Forsyth. Most fish
were taken from July through October during 1975 and 1976, using several
methods. The majority were captured by electrofishing at Miles City and Intake,
although fish were taken in seine hauls at the same locations. Catfish from
the Tongue River were trapped. Some burbot were caught by fishermen near
Forsyth in January. Sampling was limited primarily to backwaters and to
slower currents along the shore.
Digestive tracts were removed from the fish, preserved in 10 percent
formaldehyde, and taken to the laboratory for analysis. Food items from the
esophagus and intestines were not analyzed. Stomach contents were identified
to the species level when possible, using descriptions and keys by Cross (1967)
and Brown (1971). Invertebrates found in fish stomachs are listed taxono-
mically in appendix D. Many of the fish in the stomachs were digested
beyond recognition. Food items were counted and measured volumetrically by
water displacement in graduated cylinders (appendix E). Methods of analysis
are discussed by Lagler (1964).
Calculations were made to determine: (1) the percentage of stomachs in
which each food type was present (frequency of occurrence),. (2) the average
number of organisms of each type in the stomachs which contained that food
type, (3) the percentage of total number of food organisms, and (4) the
percentage of the total food volume.
Ivlev's (1961) electivity index was used to determine selection for
specific food types. The index is a forage ratio of the relative portion of
a food type in the diet to the portion that exists in the environment. It
takes the form:
E = ri -Pi
ri + pi
where ri = the relative portion of food type i in the ratio, expressed
as the percentage of the total number of food items, and
119
.-
pi = the relative portion of food type i in the environment,
expressed as the percentage of the total number of food
items available.
Values range from -1.0 to 1.0. Negative values indicate that the fish
is selecting against a food type, which means that the percentage of a
specific food organism in the ratio is lower than the percentage of the
food type in the environment. Active selection for a particular food suggests
a preference for the food and yields a positive value. A value near 0 indicates
that a fish consumes a food type in the same proportion in which it is available.
The use of the index requires knowledge of the population numbers of prey
organisms that occur in the predators' habitat. Relative abundance data for
forage fish species were not adequate for purposes of this study; therefore,
food selection by sauger and burbot, which feed primarily on forage fish,
could not be determined. Ivlev's index was used to determine selection for
benthic macroinvertebrates by shovelnose sturgeon, goldeye, and channel
catfish. The data from quantitative bottom samples of benthic organisms taken
by Robert Newell at Miles City and Intake in August and September 1975 (see
Report No. 5 in this study) were used in this study. Newell's data did not
include weight or volumetric measurements of benthos, so electivity was
determined on the basis of organism numbers alone.
Sample sizes of captured fish were too small to divide the individuals
into groups by date or location of sampling. The one exception was shovel-
nose sturgeon, which were separated into two groups by date of capture prior
to stomach analysis.
A few individuals of northern pike, carp, white sucker, smallmouth bass,
white crappie, walleye, freshwater drum, and flathead chub were also taken.
For these species, only qualitative results are listed.
FORAGE FISH SURVEY
Forage fish samples were collected.during 1974 in the vicinities of Myers,
Forsyth, Miles City, Sunday Creek, Glendive, Intake, and Sidney. The main
channel and backwater areas were sampled with a 50 foot x 6 foot x 1/4 inch
bag seine and by electrofishing. In 1975 additional samples were collected
at eight locations on the lower river: Hysham, Forsyth, Miles City, the
mouth of Sunday Creek, the mouth of the Powder River, Terry, Intake, and
Sidney. These samples were also obtained from main channel and backwater
areas. In addition to the 50 foot x 6 foot x 1/4 inch bag seine and electro-
fishing, a 100 foot x 8 foot x 1/4 inch loose-hung seine was utilized.
120
STOMACH CONTENTS
The lengths, weights, and numbers of fish collected for quantitative
stomach analysis are presented in table 42. Most of the fish were at least
two years old. Fingerlings and fry of sturgeon, burbot, sauger, and goldeye
were not captured. The results of stomach contents analyses are given in
tables 43-50 and in appendix F.
TABLE 42. Numbers, lengths, and weights of fish collected for stomach analysis.
Number of
Number of Stomachs
Fish Containing Total Length {mm) Fork Lenqth { mm) Weiqht {q)
Collected Food Range Average IKange Average l<ange Average
Shovel nose
sturgeon 41 41 330-889 533 305-826 493 100-3334 726
Gold eye 18 17 292-335 312 159-354 259
Channel
catfish 47 20 236-742 495 109-4763 1279
Burbot 22 13 318-645 421 136-1515 367
Sauger 114 43 201-546 295 41-1052 236
All sturgeon stomachs contained food items. Digestion in the sturgeon
was apparently slow, because food organisms were usually intact and relatively
easy to identify. At the other extreme, digestion in the sauger stomachs was
rapid; only 43 of 114 stomachs contained food, much of which was difficult or
impossible to identify.
SAUGER
Small forage fish were, in general, the dominant staple of the larger
sauger (table 43). Channel catfish fry were the most abundant of the forage
fish in the diet. Although the channel catfish is a game species, for the
purpose of this study, any fish of sufficiently small size to be ingeested
by predators is considered a forage fish. Catfish volume was exceeded by
that of flathead chub, longnose dace (Rhinichthys cataractaeJ, and stonecats
(Noturus f~vusJ. Most of the unidentified fish and fish remains, 38.4 per-
cent of the volume, probably consisted of species listed in table 43. Except
121
TABLE 43. Stomach contents of 43 sauger collected from the lower Yellowstone
River during 1975 and 1976.
Average
Number of
Organisms
Frequency in Stomachs Percentage Percentage
of Containing of Total of Total
Food Type Occurrence Them Number Volume
FISH
Shovelnose sturgeon 2.3 1.0 0.6 1.7
Flathead chub 9.3 1. 5 3.3 20.3
Sturgeon chub 4.7 2.0 2.2 3.4
Longnose dace 9.3 1.5 3.3 10.3
Minnow (HybognathusJ 7.0 1.0 1.7 3.1
Channel catfish 18.6 1.4 6.1 7.9
Stonecat 2.3 1.0 0.6 13.0
Unidentified fish
and remains 58.1 38.4
. TOTAL 98.1
INVERTEBRATES
TravereZ~ aZbertana 11.6 28.2 77.9 1.5
Heptagenia eZegantu~ 2.3 1.0 0.6 0.0
Ephoron aZbwn 2. 3 1.0 0.6 0.0
Hydropsychidae 9.3 1.5 3.3 0.1
Unidentified insect
parts 9.3 0.1 r--------------------------------------TOTAL 1.7
MISCELLANEOUS
Woody debris 7.0 0.2
122
for catfish and stonecats, which were readily identified, the percentages given
for the forage species are probably low due to the large volume of unidentified
fish parts.
Aquatic macroinvertebrates were found mainly in the smaller sauger.
Insects, of which TravereZZa aZbertana, the only TravereZZa species in the
lower Yellowstone, was the most abundant, accounted for 1.7 percent of the
food, a low percentage because few small fish were taken. Lengths of sauger
ranged from 201 to 546 mm (7.gl to 21.50 in). Sauger containing only insects
in their stomachs averaged 246 mm (9.69 in); those which ate only fish averaged
300 mm (11.81 in). No sauger over 282 mm (11.10 in) in length contained
insects. The evidence suggests that macroinvertebrates are an important food
only for young sauger. It is expected that insects form the major portion of
the diet in fry and fingerlings. Priegel (1970) found that most of the insects
consumed by sauger and walleye in Lake Winnebago, Wisconsin, were taken by
fish under 275 mm (10.83 in) in length. In another lake study, Nelson (1968)
observed that sauger fry feed on zooplankton and some insects until they attain
lengths of 70 to 100 mm (2.76 to 4.33 in). Beyond .this length, fish become
more important in the diet. Cross (1967} and Brown (1971) state that the
food of young sauger is almost entirely aquatic insects.
BURBOT
Table 44 shows that 94.0 percent.of the volume in burbot stomachs consisted
of fish. The major prey species were flathead chub, stonecats, and minnows of
the genus Hybognathus. The brassy minnow (H. hankinsoni), plains minnow
(H. pZacitus) and silvery minnow (H. nuchaZis) are the only species of
Hybognathus present in the lower Yellowstone River (Brown 1971).
Benthic insects formed 3.0 percent of the food volume of burbot. As
with the sauger, insects occur more frequently in the diet of small fish.
The smallest burbot captured for this study was 318 mm (12.52 in). Studies by
a number of researchers agree that insects and other invertebrates are the
·dominant foods of first-year burbot (Bailey 1972, Bjorn 1940, Hewson 1955,
Lawler 1963, Miller 1970, and Volodin and Ivanova 1969}.
CHANNEL CATFISH
Aquatic and terrestrial insects were the most abundant food types of the
channel catfish (table 45}. Mayflies, especially TravereZZa, and grasshoppers
composed a large part of the insect bulk. It was noted that many of the
TravereZZa were emergent adults. Several stomachs contained a large number
of small Hymenoptera. Only two fish were found in the stomachs of catfish,
one of them a large shorthead redhorse (Moxostoma macroZepidotum) which dis-
placed 396.0 ml of water. The volume percentages of food types were dis-
torted by the presence of the shorthead redhorse; table 45 shows that insects
accounted for 25.6 percent of the volume, but, if the sucker were not included,
the insect volume would increase to 60.8 percent.
123
TABLE 44. Stomach contents of 13 burbot collected from the Yellowstone River
below Miles City in January 1976.
Average
Number of
Organisms
Frequency in Stomachs Percentage Percentage
of Containing of Total of Total
Food Type Occurrence Them Number Volume
FISH
Carp 7.7 2.0 3.4 6.5
Flathead chub 23.1 3.7 19.0 27.3
Sturgeon chub 7.7 1.0 1.7 0.9
Minnow (Hybognathus) 38.5 1.6 13.8 15. 1
Flathead minnow 7.7 1.0 1.7 5.4
Sucker (Catostomidae) 7.7 1.0 1.7 3. 1
Stonecat 23.1 2.7 13.8 11.4
Unidentified fish and
remains 61.5 24.2
TOTAL 94.0
INVERTEBRATES
Isogenus sp. 7.7 13.0 22.4 2.2
Hydropsychidae 15.4 4.5 15.5 0.2
Rhithrogena unduZata 15.4 2.0 6.9 0.1
Unidentified insect
parts 15.4 0.5
TOTAL 3.0
MISCELLANEOUS
Algae 7.7 0.7
Gravel 23. 1 2.3
TOTAL 3.0
Orthoptera, Hymenoptera, and TravereZZa nymphs and imagoes were present in
large numbers during the period of collection but are rare during the remainder
of the year. These insects were probably taken from the water surface by
catfish, suggesting that this fish is an opportunist. The catfish is likely
to alter its food habits considerably during other seasons as food composition
changes. Brown (1971) states that the channel catfish is omnivorous and eats
whatever is available.
124
,
I
TABLE 45. Stomach contents of 20 channel catfish collected from the Yellowstone
River near Miles City and Intake and from the mouth of the Tongue River from
July through September, 1975 and 1976.
Average
Number of
Organisms
Frequency in Stomachs Percentage Percentage
of Containing of Total of Total
Food Type Occurrence Them Number Volume
INVERTEBRATES
Ephemeroptera
Baetis spp. 10.0 3.5 o. 1 0.0
Hepta{Jenia eZegantula 5.0 7.0 0.1 0.0
Rhithrogena unduZata 5.0 7.0 0. 1 0.0
TravereZZa aZbertana so:o Sill . 8 88.5 16.4
Ephoron aZbwn 5.0 1.0 0.0 0.0
Trichoptera
Hydropsychi dae 60.0 9.3 1.7 0.3
Plecoptera
Isoperla spp. 5.0 4.0 o. 1 0.0
Diptera
Chironomidae 20.0 18.5 1 . 1 0.1
SimuZiwn sp. 10.0 24.5 0.7 0.1
Hemiptera
Corixidae 5.0 1.0 0.0 0.0
Coleoptera a 10.0 1.0 0.0 0.0
Hymenopteraa 20.0 88.8 5.4 0.2
Orthopteraa 40.0. 16.3 2.0 3.8
Oligochaeta 10.0 3.5 0.1 0.0
Unidentified insect parts 65.0 4.7
TOTAL 25.6
FISH
Shorthead redhorse 5.0 1.0 0.0 65.5
Stonecat 5. 0 1.0 0.0 1.7
Unidentified fish remains 20.0 1.0
TOTAL 68.2
MISCELLANEOUS
Bird 5. 0 1.0 o.g 3.6
Algae 10.0 2.0
Vascular plant materials 10.0 0.4
Rocks 10.0 0.2
TOTAL 6.2
a Terrestrial
125
It has been shown in other studies that insects are significant in the
catfish diet. Stomachs of channel catfish from the Mississippi River in
Iowa contained a dominance of insects, of which 68.0 percent were Hexagenia
nymphs, a still-water bottom burrower, and imagoes of the same species
{Hoopes 1960). Hoopes ~ollected catfish from April to October, during the
peak of insect emergences. In another study, also conducted from April
through October, Bailey and Harrison {1948) found that insects were an.
important part of the diet of the southern channel catfish (Ictalurus
~tris punctatusJ; 98 percent of the stomach volume of catfish up to
100 mm {3.94 in) consisted of insects. For fish exceeding 300 mm {11.81 in),
the insect volume was 28.0 percent, and the fish volume was 35.0 percent.
GOLDEYE
Goldeye fed almost exclusively on insects {table 46). TravereZLa
albertana, the dominant aquatic species, accounted for 70.5 percent of the
volume of identified insects. This was similar to Hoopes' (1960) results
in which 56.0 percent of the goldeye diet consisted of Hexagenia nymphs,
another Ephemeroptera genus. Grasshoppers were also present in many goldeye
stomachs from the Yellowstone River. More than 52.0 percent of the total
volume consisted of unidentified insect parts, which implies that digestion
occurs rapidly in the goldeye.
SHOVELNOSE STURGEON
As with the goldeye, insects comprised more than 95.0 percent of the
stomach contents of shovelnose sturgeon. Sturgeon collected in May and June
had fed heavily on hydropsychid caddisflies {table 47). In most stomachs~
the heads of caddis larvae were separated from the bodies, and generic
identification was not possible. The larval bodies were complete in two
stomachs which contained a total of 491 Hydropsyche, 7 Cheumatopsyche,
and 53 damaged caddis larvae.
Hydropsychid caddisflies were present in 90.5 percent of the stomachs
of sturgeon captured from July through September (table 48), but amounted to
only 1.9 percent of the volume. During this period, TravereZLa, the primary
food organisms, comprised 46.2 percent of the diet.
Fine gravel particles were present in several sturgeon stomachs. Most of
this material was from the pupal cases of Trichoptera.
In a one-year study of food habits of the shovelnose sturgeon in the
lower Missouri River, Moode (1973) found that chironomid larvae formed the
bulk of the sturgeon diet from April through September. During the remainder
of the year, Hydropsyche was the dominant food organism. Sturgeon stomachs
collected by Held (1966) in June contained a chironomid volume of almost
54.0 percent. Hydropsychid larvae accounted for 75.0 percent of the sturgeon
diet in the Mississippi River (Hoopes 1960).
126
,
I
I
TABLE 46. Stomach contents of 17 goldeye collected from the Yellowstone River
at Miles City in August, 1975 and 1976.
Average
Number of
Organisms
Frequency in Stomachs Percentage Percentage
of Containing of Total of Total
Food Type Occurrence Them Number Volume
INVERTEBRATES
Ephemeroptera
Baetis spp. 23.5 7.5 3.8 0.8
Heptagenia eZegantuZa 5.9 1.0 o. 1 0.0
Hhithrogena unduZata 17.6 1.3 0.5 0.1
TravereZZa aZbertana 35.3 99.7 74.9 32.0
EphemereZZa inermis 5.9 11.0 0.1 0.0
Trichoptera
Hydropsychidae 35.3 4.5 3.4 1.0
Plecoptera
Isogenus spp. 5.9 1.0 0.1 0.0
IsoperZa spp. 5.9 2,0 0.3 0.1
Diptera
Chironomidae 29.4 7.2 4.5 0.6
Tipulidae 5.9 1.0 0.1 0.3
Hemiptera
Corixidae 17.6 2.7 1.0 0.7
Coleoptera
Dytiscidae 5.9 1.0 0.1 0.0
Odonata
Coenagrionidae 5.9 1.0 0.1 0.6
Orthopteraa 58.8 1.3 1.6 8.2
Hymenoptera a 5.9 74.0 9.3 0.9
Unidentified insect parts 100.0 52.4
TOTAL 97.7
MISCELLANEOUS
Vascular plant materials 23.5 2.3
a Terrestrial
127
TABLE 47. Stomach contents of 20 shovelnose sturgeon collected from the
Yellowstone River near Miles City and Intake during May and June, 1975 and 1976.
Food Type
Ephemeroptera
Baetis spp.
Heptagenia eZegantula
Rhithrogena unduZata
EphemereZZa inermis
Trichoptera
Hydropsychidae
Plecoptera
Isogenus spp.
Isoperla spp.
Diptera
Chironomidae
Simulium sp.
He:r:atoma sp.
Atherix variegata
Oligochaeta
Col eopteraa
Unidentified insect parts
TOTAL
Vascular plant material
Rocks
TOTAL
a Terrestrial
Frequency
of
Occurrence
70.0
45.0
25.0
30.0
100.0
70.0
75.0
95.0
15.0
60.0
5.0
10.0
5.0
100.0
25.0
30.0
Average
Number of
Organisms
in Stomachs Percentage
Containing of Total
Them Number
INVERTEBRATES
13.4 5.6
18.1 4.9
1.8 0.3
12.5 2.2
76.1 45.7
5.1 2.2
41.9 18.8
32.7 18.6
1.0 0.1
4.0 1.4
1.0 0.0
1.5 0.1
1.0 0.0
MISCELLANEOUS
128
Percentage
of Total
Volume
1.8
2.6
0.1
1.4
34.7
8.3
4.B
2.6
0.0
0.9
0.1
0.0
0.0
38. 1
95.4
2.2
2.4
4.6
'
TABLE 48. Stomach contents of 21 shovelnose sturgeon collected from the
Yellowstone River below Intake from July to September, 1975 and 1976.
Food Type
Ephemeroptera
Frequency
of
Occurrence
Baetis spp. 100.0
Heptagenia elegantula 28.6
Rhithrogena unduZata 19.0
TravereZZa albertana 95.2
EphemereZZa inermis 4.8
Tricorythodes minutus 9. 5
Ephoron album 4.8
Trichoptera
Hydropsychidae 90.5
LeptoceZZa sp. 4.8
Plecoptera
Isogenus spp. 19.0
IsoperZa spp. 14.3
Diptera
Chi ronomidae 90.5
Simulium sp. 66.7
Odonata
Gomphidae 4.8
.Hemiptera
Corixidae 4.8
Orthopteraa 9.5
Hymenopteraa 9.5
Average
Number of
Organisms
in Stomachs
Containing
Them
Percentage
of Total
Number
INVERTEBRATES
32.1 12.5
1.8 0.2
8.8 0.6
106.5 39.4
1.0 0.0
7.5 0.3
1.0 0.0
5.5 1.9
21.0 0.4
1.8 o. 1
2.3 0.1
107.2 37.7
25.2 6.5
1.0 0.0
1.0 0.0
1.0 0.0
2.5 0.1
Percentage
of Total
Volume
4.7
0.2
0.4
46.2
0.0
0.1
0.0
1.9
1.1
0.1
0.1
4.5
2.4
0.0
0.0
0.2
0.1
Unidentified insect parts ._l.:..;O;.:O;.;. . .;:.o _______________ ~7 __
TOTAL r
35.5
97.5
Vascular plant materials
Algae
Rocks
TOTAL
a Terrestrial
g,5
9.5
19.0
MISCELLANEOUS
0.9
0.5
1.1
2.5
129
TABLE 49. Food types of miscellaneous fish species.
Food Type
Fish
F1 a thead chub
Sturgeon chub
Channel catfish
Unidentified fish remains
Invertebrates
Baetis
T:rovere Z Za
Heptagenia
Rhithrogena
Ephoron
Hydropsychidae
Chironomidae
SimuUwn
Unidentified insect parts
Organic detritus
Northern White
Pike (2) Carp (1) Sucker (1)
X
X
X
X
X
X
X
X
X
Small mouth
Bass (3)
X
X
X
White
Crappie (1) Walleye (1)
X X
Freshwater
Drum (2)
X
X
X
X
X
X
X
X
X
NOTE: The number of fish sampled of each species is given in parentheses after the name of each species
above.
_ .. ___ _
r
FLATHEAD CHUB
The stomach contents of 19 flathead chub were removed and analyzed
qualitatively. Food organisms were well digested. An estimated 40-50
percent of the volume consisted of Cladocera. The remainder included remains
of Corixidae, Hydropsychidae, Iaogenus, and unidentified organisms.
OTHER SPECIES
The qua.litative results of stomach analyses for miscellaneous fish species
is presented in table 49. Forage fish were found in the stomachs of northern
pike, smallmouth bass, white crappie, and walleye. The carp, white sucker,
and freshwater drum fed on insects and organic detritus.
FOOD SELECTION
The values for Ivlev's electivity index (E) were calculated for the major
benthic food organisms eaten by shovelnose sturgeon, goldeye, and channel
catfish (table 50). The shovelnose sturgeon and goldeye selected for Baetis
and Chironomidae, but selected against Heptagenia, Rhithrogena, and
Hydropsychidae. The sturgeon consumed Travere~~ in proportions equal to
its availability, while the goldeye showed preference for Travere~~a.
Travere~~a nymphs and adults on the water surface were preferred by channel
catfish over other aquatic species during the study period. Sturgeon and
goldeye select for insects characteristic of a riffle habitat, while catfish
appear to take advantage of plentiful food types in any habitat.
TABLE 50. Ivlev's electivity index for benthic food organisms eaten by
shovelnose sturgeona, goldeye, and channel catfish.
Shovel nose
Food Type Sturgeon Goldeye Channel Catfish
Baetis 0.58 0. 15b -0.99b
Heptagenia -0.43bC -0.92b -o.8sg
m,ithrogena -0.6ob -0.65 -0.83
Travere~~ -0.04 0.63 0.76
Hydropsychidae -0.88 -0.78 -0.92
Chironomidae 0.81 0.40 -0.75
SimuZiwn 0.78C -1.oob -0.79b
a Because relative abundances of insects were unknown for these months,
sturgeon collected in May and June were excluded.
b Less than 1 percent of benthic food items
c Less than 1 percent of benthic population
131
Selection for food types is difficult to measure. Preferences for
aquatic organisms may vary seasonally as larvae grow in size or emerge as
adults. Unfortunately, fish were not collected during all seasons. During
the period of capture, TravereZLa nymphs were mature while other species such
as Hydropsyche were relatively small. Food habits of the insect-feeding fish
species may be different during the winter and spring months when caddis
larvae are approaching mature size and TravereZLa nymphs and terrestrial
insects are rarely available.
Ivlev's index and other forage ratios are based on the relative portions
of food organisms that occur in the environment, but not all foods are
readily available to a predator (Leonard 1941). Baetis, a fast swimmer, is
capable of functioning in fast water without the protection of the bottom
substrate. Baetia, ·therefore, was accessible to sturgeon and go 1 deye.
Heptagenia and Rhithrogena are capable of crawling beneath stones where they
are unavailable to predators. Hydropsychid larvae are found in rock crevices
or between stones, but may also be exposed on rock surfaces. Chironomid larvae
are somewhat immobile and vulnerable to predators (Hess and Swartz 1941,
Klarberg and Benson 1975).
The present study illustrates the importance of aquatic insects in the
diets of sturgeon, goldeye, and catfish. The sturgeon was restricted to
bottom insects of riffles. The goldeye fed exclusively on insects as well
and included a small amount of terrestrial insects in the diet. Insects were
significant in the catfish diet, but some fish were also taken. Young
sauger and burbot were highly dependent on macroinvertebrates for their food
source. Insects were present in the stomachs of carp, white sucker, and
freshwater drum. Other common fish species of the lower Yellowstone River
which are dependent on aquatic macroinvertebrates for a large portion of their
diet include longnose sucker (Catostomus catostomus), shorthead redhorse,
river carpsucker (Carpoides carpio), blue sucker (Cycleptus elongatus),
smallmouth buffalo (Ictiobus bubalus), bigmouth buffalo (I. cyprinellus),
black bullhead (Ictalurus melaa), and stonecat. Insects were also important
foods for young individuals of crappie, bass, and walleye (Brown 1971).
Little is known of the habitat requirements and foods of forage fish of
the lower river. During the period of study, the flathead chub appears to
depend on the backwaters for its food supply of Cladocera and insects. This
species is abundant in the river and is a common food item of predator species.
In the genus Hybognathua, the silvery minnow inhabits backwater areas
(Cross 1967) and feeds on bottom ooze and algae (Brown 1971). The plains
minnow and brassy minnow are common in small streams and the slow waters of
large rivers. Their food habits are similar to those of the silvery minnow.
Unlike many of the
fast water of riffles.
(Brown 1971).
forage species, the longnose dace is adapted to the
Insect larvae are the main food of ·this species
FORAGE FISH SURVEY
Results of the forage fish survey are presented in table 51. The most
common species, the flathead chub and emerald shiner, frequently occur in both
132
,
~
w w
-
TABLE 51. Forage fish species list for lower Yellowstone River showing location, date of collection,
and habitat sampled.
Location
Below Myers Bridge
Across from mouth
of Tongue
Across from mouth
of Tongue
Mouth of Sunday
Creek
Glendive
Hysham
Be 1 ow Forsyth
BACKWATER
Date
10-30-74
7-23-74
10-23-74
9-12-74
10-9-74
10-10-74
10-18-74
9-29-75
9-29-75
Species
Emerald shiner
Plains minnow
Plains minnow
Emera 1 d shiner
Brassy minnow
Plains minnow
Sturgeon chub
Flathead chub
Flathead chub
Flathead chub
Emerald shiner
Lake chub
Emerald shiner
Mountain sucker
Flathead chub
Emera 1 d sh i ner
S 11 very minnow
Fathead minnow
mountain sucker
._ -"'
MAIN CHANNEL
Location Date
Below Rosebud Diversion 10-17-74
Above Miles City 7-25-74
Below Tongue 10-16-74
Across from Hysham 9-29-75
Backwater
Across from arid above
mouth of Tongue River
Below Terry
Below Powder River
Intake
7-24-75
9-30-75
9-30-75
8-21-75
9-18-75
Species
Emerald shiner
Plains minnow
Emerald shiner
Flathead chub
Mountain sucker
Mountain sucker
Flathead chub
Plains minnow
Flathead chub
Lake chub
Mountain sucker
Longnose dace
Flathead chub
Flathead chub
Emerald shiner
Si 1 very minnow
Flathead chub
Fathead minnow
Plains minnow
Sturgeon chub
Emerald shiner
Emerald shiner
Flathead chub
Longnose dace
Sturgeon chub
-
'
,
backwaters and main channel areas. Two species previously reported from the
Yellowstone (Brown 1971), the pearl dace (Semotilus margarita) and creek chub
(S. atromaculatusJ, were not taken during this survey. Brown called the
creek chub "quite rare" and the pearl dace not abundant.
·Notably absent from the forage fish collections is the stonecat.
Stonecats generally prefer swift-current riffle areas with large gravel or
cobble substrates (Trautman 1957). Available techniques were inadequate
for such areas. Although not collected during current sampling, stonecat are
common in the lower Yellowstone and are an important forage fish for some
species. A forage fish species list for the lower Yellowstone is included
in appendix G.
135
r
r
This study investigated not only the food preferences of river fishes but
also the importance of all organisms in the food chain of the river ecosystem.
Fish species adaptations and preferences for particular habitats are often
related to their food habits. Research of food habits assists in an under-
standing of the interrelationships among organisms and their environment.
Impacts on one segment of an ecosystem can affect other segments.
Impacts on fish populations from reduced flow vary for each species
depending on food habits. Riffle insects provide food for sturgeon, goldeye,
catfish, longnose dace, and for immature burbot and sauger. Mature sauger,
burbot, and catfish rely (in part) on the backwater areas for their supply
of forage fish. Reduced flow would affect both riffles and backwaters.
RIFFLE HABITAT
Riffle insects rely on current for food, oxygen, and protection from
predators. Reduced discharge is detrimental to benthic populations because:
(1) velocity requirements of riffle species are no longer met and (2) the
wetted bottom area of the channel is decreased. R. L. Newell (see Report No. 5
in this series) estimated that insect density at Intake could decrease by
10 percent for each 28.3 m3/sec (1000 cfs) reduction in discharge below
255m3/sec (gooo cfs).
Insects which prefer the greatest velocities, such as TravereLla and
Hydropsyahe, would be among the first organisms to feel the impact of reduced
flows. According to Report No. 5 in this series, peak densities of TravereLLa
occurred at .69 m/sec (2.25 ft/sec) in August and .76 m/sec (2.5 ft/sec) in
October. Numbers of Hydropsyahe were highest at velocities of .46 m/sec (1.5
ft/sec) in October and .61 m/sec (2 ft/sec) in November. Faster currents are
preferred by caddis larvae in later months as they grow in size.
Low flows decrease the wetted perimeter of the river channel. The loss
of habitable space varies with the depth and width of the channel, the greatest
reduction occurring where riffles are wide and shallow. Insects are concen-
trated in higher densities as flows diminish. Glass and Bovbjerg (lg69) found
that when numbers of Cheumatopsyche larvae are high, aggression among individuals
maintains tolerable spacing. Invertebrates remove from riffles by drifting
when flows are reduced (Minshall and Winger 1968, Pearson and Franklin 1g68).
This study has shown that TravereLLa was the most important food item
of goldeye, catfish, and sturgeon during August and September. TravereLla
aLbertana comprised 60 percent of the number of benthic fauna at Intake in
August (Report No. 5). Due to the high density of this mayfly species and
its water velocity preference, a reduction in TravereLla numbers could be a
critical loss to insect-feeding fish during abnormally low flows in late
summer.
137
At Intake, TravereZZa relative abundance declined from 60 percent in
August to less than 1 percent in November, while Hydropsyche increased from
14 percent of the organisms to 54 percent during the same period (Report No. 5).
With the loss of TT'avereZZa, Hydropsyche becomes the dominant food item in
the riffle habitat. Hydropsychids were the major food item of sturgeon
captured from the Yellowstone in May and June. Hoopes (1960) and Modde (1973)
also point out the importance of Hydropsychids in the sturgeon diet.
Hydropsyche, being sensitive to changes in velocity (Edington 1965 and 1968),
may be affected more adversely than most other riffle species. A reduction
in hydropsychids could, by altering food habits, be detrimental to fish that
feed in the riffles, especially the shovelnose sturgeon, which is highly
adapted for riffle feeding.
In addition to reducing numbers of food organisms, a drop in discharge
concentrates fish into a smaller habitat. Forage fish and the remaining
benthic organisms become more vulnerable to predation from the high-density
fish community. Decreased food and space can limit the fish population growth
to the point that predator biomass may decline in amounts equal to the loss of
riffle insect biomass.
SLOW-WATER HABITAT
The specific habitat requirements of forage and game fish species of the
Ye 11 owstone are not known, but 1 arge numbers of forage fish, burbot, sauger,
and catfish were collected in the backwaters and slow littoral waters. To
maintain the present populations of carnivorous species, it is necessary to
preserve the backwater habitats. Backwaters are common to the braided
section of the river. A dominant discharge (that high flow recurring every
1~ to 2 years which, through a combination of magnitude and frequency,
accomplishes the most geomorphic work 1n a channel over the long term) is
necessary to retain the characteristics of the main and side channel
morphology. Periodic flows in the side channels prevent the invasion of
riparian vegetation. Without side channels, backwaters would fill with silt,
causing a reduction in wetted perimeter and depth, eventually destroying the
backwater habitat. Martin (see Report No. 2 in this series) reports a 43
percent reduction in the number of islands on the Bighorn River as a result
of reduced flows due to water impoundments. Islands became part of the
mainland, eliminating the side channels and backwaters. Similar results
could be expected on the lower Yellowstone following reduction of spring
flows, changing the river from a braided to a meandering stream.
Even if sufficient flows were preserved to maintain the existence of
side channel flow during the spring runoff, it would still be necessary to
ensure that the needed volume of water is available to keep the backwaters
full during the remainder of the year to maintain slow-water habitat.
The growth rate of most aquatic organisms is greatest during summer months
when water temperatures are at a peak (Hynes 1970). During this period of
receding flows and heavy water diversions for irrigation, food and habitable
area are of critical importance to the growth of insects and fishes. The
most severe impacts on aquatic communities are likely to occur if excessive
water withdrawals are made during August and September.
138
1
Discharge of the Yellowstone is lowest during winter months prior to
spring runoff. Excessive water withdrawals for industrial use in this
period of low flow would take its toll on benthic organisms. This would result
not only from further reductions in velocity and wetted bottom area, but from
the increased dangers of ice accumulation. Formation of anchor ice in riffle
areas at night tends to impede the flow. As ice melts during the day, the
churning a·ction of loose ice scours the benthos, removing algae, detritus,
and invertebrates (Hynes 1970, Maciolek and Needham 1951).
139
Fish of several species were collected from the Yellowstone River near
Miles City and Intake. Most of them were captured by electrofishing in August
of 1975 and 1976. Stomach contents from 145 mature fish were identified,
counted, and measured volumetrically. Quantitative results were tabulated for
shovelnose sturgeon, goldeye, channel catfish, sauger, and burbot.
Insects were the major foods of sturgeon, goldeye, and catfish. Aquatic
insects of riffles were of greatest importance to all three species but were
consumed in greatest amounts by shovelnose sturgeon. Goldeye and catfish
stomachs contained terrestrial insects as well. Only the catfish diet included
fish.
From a previous study of the aquatic food organisms available in August
and September, Traverella aZbertana was the most abundant (Report No. 5
in this series). lvlev's electivity index revealed that this species of
mayfly was eaten by sturgeon in portions equal to its availability, but
goldeye and catfish selected it over other foods.
Hydropsyahe is the dominant species of riffle insects during the fall and
winter months on the river (Report No. 5). Based on that fact and on the
results of studies in other rivers, it is expected that this genus of caddis-
fly becomes the major food item of sturgeon following the emergence of
TravereZZa in September.
Flathead chubs and minnows of the genus Hybognathus were common in the
diets of sauger and burbot. In addition, sauger stomachs contained longnose
dace and catfish fry. Stonecats were important in the burbot diet. Young
sauger and burbot are highly dependent on invertebrates for food.
The impact of reduced flows would be felt by all members of the food
chain. Traverella and Hydropsyahe, the most abundant benthic insects, are
the most important foods of riffle fishes and prefer relatively high water
velocities; they would suffer the greatest loss during low flows. As food
and riffle space declines, fish growth is restricted until predator populations
stabilize or fall to levels that can be supported by the altered habitat. Of
the fish that feed on benthic insects, reduced flows would be most detrimental
to the growth and production of shovelnose sturgeon, goldeye, channel catfish,
and young-of-the-year sauger and burbot.
The maintenance of side channels and backwaters is dependent on high
spring flows. As side-channel flow·diminishes in late summer, sufficient dis-
charge must remain to ensure the existence of backwater areas. A reduction in
backwaters would result in a direct loss of habitat to fish species which
frequent these still waters. Piscivorous species affected by such alteration
include mature sauger and burbot, channel catfish, northern pike, and crappie.
141
143
PROJECTIONS OF FUTURE USE
FIGURES
A-1. The Nine Planning Subbasins of the Yellowstone Basin. . . . . . 147
TABLES
A-1. Increased Water Requirements for Coal Development
in the Yellowstone Basin in 2000. . . ..
A-2. The Increase in Water Depletion for Energy
by the Year 2000 by Subbasin ....... .
A-3. Feasibly Irrigable Acreage by County and Subbasin
by 2000, fligh Level of Development ..... .
A-4. The Increase in Water Depletion for Irrigated Agriculture
by 2000 by Subbasin . . . . . . .
A-5. The Increase in Water Depletion for Municipal Use by 2000
A-6. The Increase in Water Depletion for Consumptive Use
by 2000 by Subbasin . . . .
145
.
147
14B
149
150
150
151
.In order to adequately and uniformly assess the potential effects of water
withdrawals on the many aspects of the present study, projections of specific
levels of future withdrawals were necessary. The methodology by which these
projections were done is explained in Report No. 1 in this series, in which
also the three projected levels of development, low, intermediate, and high, are
explained in more detail. Summarized belm~. these three future levels of
development were formulated for energy, irrigation, and municipal water use
for each of the nine subbasins identified in figure A-1.
ENERGY WATER USE
In 1975, over 22 million tons of coal (19 million metric tons) were mined
in the state, up from 14 million (13 million metric) in 1g74, 11 million (10
million metric) in 1973, and 1 million (.9 million metric) in 1969. By 1980,
even if no new contracts are entered, Montana's annual coal production will
exceed 40 million tons (36 million metric tons). Coal reserves, estimated at
over 50 billion economically strippable tons (45 billion metric tons) (Montana
Energy Advisory Council 1976), pose no serious constraint to the levels of
development projected, which range from 186.7 (170.3 metric) to 462.8 (419.9
metric) mil 1lion tons stripped in the basin annually by the year 2000.
Table A-1 shows the amount of coal mined, total conversion production,
and associated consumption for six coal development activities expected to take
place in the basin by the year 2000. Table A-2 shows water consumption by sub-
basin for those six activities. Only the Bighorn, Mid-Yellowstone, Tongue, Powder,
and Lower Yellowstone subbasins would experience coal mining or associated
development in these projections.
IRRIGATION WATER USE
Lands in the basin which are now either fully or partially irrigated total
about 263,000 ha (650,000 acres) and consume annually about 1,850 hm3 (.1,5 mmaf)
of water. Irrigated agriculture in the Yellowstone Basin has been increasing
since 1971 (Montana DNRC 1975). Much of this expansion can be attributed to
the introduction of sprinkler irrigation systems.
After evaluating Yellowstone Basin land suitability for irrigation, con-
sidering soils, economic viability, and water availability (only the Yellowstone
River and its four main tributaries, Clarks Fork, Bighorn, Tongue, and Powder,
were considered as water sources), this study concluded that 95,900 ha (237,000
acres) in the basin are financially feasible for irrigation. These acres are
identified by county and subbasin in table A-3; table A-4 presents projections
of water depletion.
Three levels of development were projected. The lowest includes one-third,
the intermediate, two-thirds, and the highest, all of the feasibly irrigable
acreage.
146
1 Upper Yellowstone
2 Clarks Fork Yellowstone
3 Billings Area
4 Bighorn
5 Mid -Yellowstone
6 Tongue
7 Kinsey Area
8 Powder
9 Lower Yellowstone
\
Figure A-1. The nine planning subbasins of the Yellowstone basin.
I • ~~ ,.
0
----\~
TABLE A-1. Increased water requirements for coal development in the Yellowstone
Basin in 2000.
level of
Development
low
lntennediate
High
low
Intennediate
High
low
lntenne'diate
Hfgh
Electric
Generation
8.0
24.0
32.0
2000 n?.ol
6000 rnw
8000 ll1\rl
30.000
90.000
120.000
I
·Coal Development Activity
Gastft-I
cat ion Sync rude l
COAL MINED (r:mt/y)
7.6 0.0
7.6 o.o
22.8 36.0
CO:IVERS!Dr~ PRODUCTION
250 rrrncfd 0 b/d
250 IIT.ICfd 0 b/d
Fertil
1 izer
0.0
0.0
3.5
0 t/0
0 t/d
750 rrrncfd 200.000 b/d 2300 t/d
WATER (Q,'jSUMPTIO:I (af/y)
9,000 0 0
9.000 0 0
27,000 58.000 13.000
CONYERSIO~S: I mt/y (short) • .907 rrr..t/y (metric)
I af/y-.Q0\23 "rnl/y
I Strip
Export />lining
171. I
293.2
368.5
• 9.350
3\,910 16.250
80.210 22.980
aNo water consumption is shown for export under the low level of develo!)1'ent because, for that
develop.':lenl level, it is assut:~ed thoU all e;o:pol"t fs by rail, rather than by slurry pipeline.
147
Tot a 1
186.7
324.8
462 .a
48.350
147.160
321.190
TABLE A-2. The increase in water depletion for energy by the year 2000
by subbasin.
INCREASE II~ DEPLETIOI~ (af/_y)
Uec. Gasifi-Syn-Ferti-Strip
Subbasin Generation cation crude lizer Export Mining Tot a 1
LOl-l LEVEL OF OEVELOPI~ENT
Bighorn 0 0 0 0 0 B60 860
Mid-Yello>~stone 22,500 9,000 0 0 0 3,680 35,1BO
Tongue 7,500 0 0 0 0 3,950 11 ,450
Powder 0 0 0 0 0 860 860
Lower Yellowstone 0 0 0 0 0 0 0
Total 30,000 9,000 9,350 48,350
INTERI~EDIATE LEVEL OF OEVELOPI~ENT
Bighorn 0 0 0 0 4,420 1 ,470 5,890
Mid-Yello>~stone 45,000 9,000 0 0 15.380 6,110 75,490
Tongue 30,000 0 0 0 9,900 7,000 46,900
Powder 15,000 0 0 0 2,210 1 ,670 18,880
Lower Yellowstone 0 0 0 0 0 0 0
Total 90,000 9,000 31,910 16,250 147,160
HIGH LEVEL OF DEVELOPMENT
Bighorn 15,000 0 0 0 11 • 100 2,050 28,150
Mid-Yellowstone 45,000 18,000 29,000 0 38.700 8,710 139,410
Tongue 45,000 9,000 29,000 0 24,860 10,170 118,030
Powder 15,000 0 0 0 5,550 2,050 22.600
Lower Yellowstone 0 0 0 13,000 0 0 13,000
Total 120,000 27,000 58,000 13,000 B0,210 22,980 321,1~0
CONVERSIONS: af/y = .00123 hm 3/y
NOTE: The four subbas1ns not sho•m {Upper Yellowstone, Billings Area, Clarks Fork
Yellowstone, Kinsey Area) are not expected to experience water depletion associated
with coal development.
148
TABLE A-3. Feasibly irrigable acreage by county and subbasin by 2000, high level
of development.
County
Park
Sweet Gras
Stillwater
Carbon
Yellow-
stone
Big Horn
Treasure
Rosebud
Powder
River
Custer
Prairie
Dawson
Richland
Wibaux
BASIN
TOTALS
Upper Clarks Bfll ings Big Hid Tongue Kinsey Po1~der lower
ellowstone Fork Area Horn Yellowstone River Area River Yellowstone
21,664
10,20.1
6.208
38,076
2.160
2.160
19.412
13.037
9.591
11 ,408
4,230
19.412 13.037 25.229
2.185
9.727
10.035
21 ,947
46.853
3,092 26,438
1,644 1,914 8.231
18.355
10,421
633
4,736 75,205 37,670
CONVERSIONS: 1 acre " .405 ha
NOTE: The number of irrfgable acres for the low and intermediate development levels are one-third
and two-thirds, respectively, of the numbers given here. This table should not be considered an exhaustive
listing of all feasibly frrigab1e acreat;~e in the Yellowstone Basin: it Includes only the acreage identified
County
Totals
21 .664
10,:!011
5,2rJ,Q
2,160
19,412
15.222
9.591
21 ,135
46.853
43,795
11 ,789
18 .355
10,421
633
237,472
as feasibly lrrigable according to the geo(jraphfc and econol"'ic constraints explained elsewhere in this report.
MUNICIPAL WATER USE
The basin's projected population increase and associated municipal water
use depletion for each level of development are shown in table A-5. Even the
13 hm3/y (10,620 af/y) depletion increase by 2000.shown for the highest develop-
ment level is not significant compared to the projected depletion increases for
irrigation or coal development. Nor is any problem anticipated in the availability
of water to satisfy this increase in municipal use.
WATER AVAILABILITY FOR CONSU~1PTIVE USE
The average annua1 yield of the Yellowstone River Basin at Sidney, r~ontana,
at the 1970 level of development, is 10,850 hm3 (8.8 million af). As shown
in table A-6, the additional annual depletions required for the high projected
level of development total about 999 hm3 (812,000 acre-feet). Comparison of
these two numbers might lead to the conclusion that there is ample water for
such development, and more. That conclusion would be erroneous, however,
because of the extreme variation of Yellowstone Basin streamflows from year
to year, from month to month, and from place to place. At certain places and
at certain times the water supply will be adequate in the foreseeable future.
But in some of the tributaries and during low-flow times of many years, water
availability problems, even under the low level of development, will be very real
and sometimes very serious.
149
TABLE A-4. The increase in water depletion for irrigated agriculture by 2000
by subbasin.
Subbasin
Upper Yellowstone
Clarks Fork
Billings Area
Bighorn
Mid-Yellowstone
Tongue
Kinsey Area
Powder
Lower Yellowstone
TOTAL
Acreage
Increase
HIGH LE.VEL OF DEVELOPMENT
38,080
2,160
19,410
13,040
25,230
21 • 950
4,740
75,200
37,670
237,480
Increase in
Depletion (af/y)
76.160
4,320
38,820.
26,080
50,460
43,900
9,480
150,400
75,340
474,960
INTERMEDIATE LEVEL OF DEVELOPMENT
BASIN TOTAL 1 158,320 316,640
LOW LEVEL OF DEVELOPMENT
BASIN TOTAL 79,160 158,320
CONVERSIONS: 1 acre = .405 ha
1 af/y = .00123 hm3fy
NOTE: The numbers of irrigated acres at the low and intermediate
levels of development are not sho~m by subbasin; however, those numbers
are one-third and two-thirds, respectively of the acres shown for each
subbasin at the high level of development.'
TABLE A-5. The increase in water depletion for municipal use by 2000.
Level of Development
Low
Intermediate
High
Population
Increase
56,858
62,940
94,150
CONVERSIONS: 1 af/y = .00123 hm3/y
150
Increase in
Depletion (af/y)
5,880
6,960
10,620
TABLE A-6. The increase in water depletion for consumptive use by 2000
by subbasin.
Increase in Depletion (af/y)
Subbasin Irrigation Energy Municipal Total
LOW LEVEL OF DEVELOP~1ENT
Upper Yellowstone 25,380 0 0 25,380
Clarks Fork 1 ,440 0 0 1 ,440
Billings Area 12 '940 0 3,480 16,420
Bighorn 8,700 860 negligible 9,560
Mid-Yellowstone 16,820 35' 180 1,680 53,680
Tongue 14,640 ll ,450 negligible 26,090
Kinsey Area 3 '160 0 0 3,160
Powder 50,140 860 360 51 ,360
Lower Yellowstone 25 '120 0 360 25,480
TOTAL 158,340 48,350 5,880 212,570
INTERMEDIATE LEVEL OF DEVELOPt1ENT
Upper Yellowstone 50,780 0 0 50,780
Clarks Fork 2,880 0 0 2,880
Billings Area 25,880 0 3,540 29,420
Bighorn 17,380 5,890 300 23,570
Mid-Yellowstone 33,640 75,490 1,360 ll0,990
Tongue 29,260 46,900 300 76,460
Kinsey Area 6,320 0 0 6,320
Powder 100,280 18,380 600 ll9,760
Lower Yellowstone 50,200 0 360 50,560
TOTAL 316,620 147,160 6,960 470,740
HIGH LEVEL OF DEVELOPMEIH
Jpper Yellowstone 76 '160 0 0 76 '160
Clarks Fork 4,320 0 0 4,320
Billings Area 38,820 0 3,900 42,720
Bighorn 26,080 28.150 480 54' 710
Mid-Yellowstone 50,460 139,410 3,840 193,710
I Tongue 43,900 ll8 ,030 780 162,710
Kinsey Area 9,480 0 0 9,480
Powder 150,400 22,600 1 '140 174,140
I
Lower Yellowstone 75,340 13,000 480 88,82C
TOTAL 474,960 321 ,1~0 10,620 806 '770 I
I
CONVERSIONS: 1 a f /y = .00123 hm3/y
151
TONGUE RIVER WATER TEMPERATURES
In general, temperatures increased wfth progression downstream. Temper-
atures greater than 21oc (7QOF) were common in the lower river; in the mid-
reach, these temperatures were near the maximum. Immediately downstream from
the dam, maximum temperatures were 22°C (720F).
FIGURES
B-1 Monthly mean of daily minimum and maximum water
temperatures for 1g74, 1975, and 1976 for the
Page
Tongue River at station Ia. . . . . . . • . . . . . . . . . . . . . 154
B-2 Monthly mean of daily minimum and maximum water
temperatures for 1975 and 1976 for the Tongue
River at station lila ....................... 155
B-3 Monthly mean of daily minimum and maximum water
temperatures for 1976 for the Tongue River at
station Vc ........................•.... 156
153
30 30 ----Maximum 30
Minimum
~ 1\ I I
I I I \
25 I I 25 25 I \
I \ I I
I I ,. I I
I \ I', I \
I \ I -I I \
I I I I I I
20 I I 20 I I 20 I \
~ I \ I I I I I.) I I I 0 I I -I I I I I .. I I I I I I ... I :::1 I I I I I -.. I I I I I I ... 15 15 15 .. I I ,, I I I I Q. I I 'I E I I I I I I
{!?. I I I I I I
U'1 ... I I I I I I ... .. I I I -I \ I .. I I I 31: 10 I 10 I 10 I
I I I I I I
I I I I I I
I I I I I I
I I I I I I
I 7 I I I I I I / I I I I 5 I I 5 \ 5 I I I I I I I I I I \ I I I I \ \ I I
I \ \
\
0 0 0
J F M A M J J A S 0 N D J F M A M J J A S 0 N D J F M A M J J A S 0 N D
1974 1975 1976
Figure B-1. Monthly mean of daily minimum and maximum water temperatures for 1974, 1975,
and 1976 for the Tongue River at station Ia.
30 ----Maximum 30
Minimum
II
I\
25 25 I \
I \
I \
I I
1\ I I
I I I \
I \ \
I I I 20 I 20 I I u I I I
0 I I I -I I I
«> I I I ~ I I ::> / I -/ I I I 0 I I ~ 15 I I 15 «> I I I I a. I I E I I
«> I I I
IJ1 1-I I I I
IJ1 ~ I I I I «> I I I I -I I I ~ 10 I I 10 I I I I I I I I I I
I I I I
I I I I
I I I I
I I I I
5 I 5 I I I I I I I I I I
I I I I
I I I I
I I
I l
0 0
J F M A M J J A 5 0 N 0 J F M AM J J A 5 0 N 0
1975 1976
Figure B-2. Monthly mean of daily minimum and maximum water temperatures
for 1975 and 1976 for the Tongue River at station Ilia.
u
0
.,
~
::J -0
~ .,
0.
E .,
1-.. ., -0
~
25
20
15
/
10 /
/
/
/
----Maximum
--Minimum
...... , / ----/ \ --" / , __ _ _ ......
/
/
/
.... -:::-;...__-./
10 20
MAY
10 20
JUNE
1976
...... -----... ........ .... '
Figure B-3. Honth1y mean of daily minimum and maximum water temperatures
for 1976 for the Tongue River at station Vc.
156
TAXONOMY OF FISH SPECIES ENCOUNTERED IN THESE STUDIES
FAMILY SPECIES
Corranon
name Scientific name Common name
Sturgeon Acipenseridae Shovelnose sturgeon
Paddlefish Polyodontidae Paddlefish
Mooneye Hiodontidae Goldeye
Trout Salmonidae Mountain whitefish
Rainbow trout
Brown trout
Pike Esocidae Northern pike
Minnow Cyprinidae Carp
Goldfish
Go 1 den sh i n·er
Pearl dace
Creek chub
Finescale dace
Flathead chub
Sturgeon chub
Lake chub
Emerald shiner
Sand shiner
Brassy minnow
Plains minnow
S i 1 very minnow
Fathead minnow
Longnose dace
Sucker Catostomidae River carpsucker
Blue sucker
Shorthead redhorse
Longnose sucker
White sucker
Mountain sue ker
157
Scientific name
ScaphiPhynchus p~toPynchus !Rafinesque)
PoLyodon spathuLa (Walbaum)
Hiodon aLosoides (Rafinesque)
PPosopium wiLLiamsoni (Girard)
SaLmo gaiPdnePi Richardson
SaLmo trutta Linnaeus
Esox Lucius Linnaeus
Cyprinus carpio Linnaeus
Carassiur. auratus (Linnaeus)
Notemigonus cPysoLeucas (Mi tchi 11)
SemotiLus margaPita (Cope)
SemotiLus atPomucu~tus (Mitchill)
Phoxinus neogaeus Cope
Hybopsis gPaciLis (Richardson)
Hybopsis geLida (Girard)
Couesius pLumbeus (Agassiz)
NotPopis atherinoides Rafinesque
1/otropis stramineus (Cope)
Hybognathus hankinsoni Hubbs
Hybognathus pLacitus Girard
Hybognathus nuchalis Agassiz
PimephaLes promeLas Rafinesque
Rhiniahthya cataractae (Valenciennes)
Carpoides carpio (Rafinesque)
cycLeptuo eLongatus (LeSueur)
Moxostoma macPoLepidotum (LeSueur)
Catootomue catostomus (Forster)
Catostomus commersoni (Lacepede)
Catostomua p~tyrhynchus (Cope)
Appendix c (Continued)
FAMILY SPECIES
~o11111on
name Scientific name Common name Scientific name
Catfish lctaluridae Black bull head Ictalurus meLas (Rafinesque)
Yellow bullhead Ictalurus natalia (LeSueur)
Channel catfish Ictalurus punctatus (Rafinesque)
Stonecat Noturuo flavus Rafinesque
Codfish Gadidae Burbot Lota lota (Linnaeus)
Sunfish Centrarchidae Rock bass Ambloplites rupestris (Rafinesque)
Green sunfish Lepomis cyanellus Rafinesque
Pumpkinseed Lepomis gibbosuo (Linnaeus)
Smallmouth bass Micropterus dolomieui (Lacepede)
Largemouth bass Micropterus salmoides (Lacepede)
White crappie Pomo:r:is annuLaris Rafinesque
Black crappie Pomoxis nigromaculatus (LeSueur)
Perch Percidae Yellow perch Perea flavescens (Mitchill)
Sauger Sti~ostedion canadense (Smith)
Walleye Stizostedion vitreum (Mitchill)
Drum Sciaenidae Freshwater drum Aplodinotus grunniens Rafinesque
SOURCE: Adapted from Brown (1971)
158
'
TAXONOMY OF INVERTEBRATES FOUND IN FISH STOMACHS
Aquatic organisms
Order Ephemeroptera (mayflies)
Family Baetidae
Ba.etis. sp.
Family Heptageniidae
Heptagenia elegantula (Eaton)
Rhithrogena wu:lulata (Banks)
Family Leptophlebiidae
Traverella albertana (McD.)
Family Ephemerellidae
EphemereZZa sp.
Family Tricorythidae
Tricorythodes minutus Traver
Family Polymitarcidae
Ephoron album (Say)
Order Plecoptera (stoneflies)
Family Perlodidae
Isogenus sp.
Isoperla sp.
Order Tri choptera ( caddi sfl ies)
Family Hydropsychidae
Cheumatopsyche sp.
Hydropsyche sp.
Order Hemiptera (bugs) ·
Family Corixidae
Order Odonata (dragonflies)
Family Gomphidae
Order Coleoptera (beetles)
Order Diptera (flies)
Family Chironomidae
Family Simuliidae
Simulium sp.
Family Tipulidae
He:r:atoma s p.
Family Rhagionidae
Atherii variegata Walker
Order Oligochaeta
Terrestrial organisms
Order Orthoptera
Order Hymenoptera
159
AVERAGE BODY VOLUME OF MAJOR ORGANiSMS FOUND IN FISH STOMACHS
Insects
Baetis sp.
Heptagenia eZegantuZa
RhithPogena unduZata
TravereZZa aZbertana
IsoperZa sp.
Isogenus sp.
Hydropsychidae
SimuZiwn sp.
Chironomidae
Fish
Hybopsis graaiZis
Hybopsis ge Zida
Hybognathus sp.
Rhinichthys cataractae
IctaZurus punctatus
Noturus [Zavus
Vol. {ml)
.0034
.0087
.0065
.0156
.0040
.0667
.0123
.0028
.0010
2.00
0.82
0.92
1.85
0.78
2.91
NOTE: These average volumes were derived by dividing the total volume
of each category of food organisms {determined by water displacement in a
graduated receptacle) by the number of organisms in each category.
161
F-1
F-2
F-3
F-4
F-5
F-6
RESULTS OF FOOD HABITS ANALYSES
OF SAUGER, BURBOT, GOLDEYE,
CHANNEL CATFISH, AND SHOVELNOSE STURGEON
TABLES
Numbers of major identifiable food items in sauger stomachs.
Numbers of major identifiable food items in burbot
stomachs collected in January ...
Numbers of major identifiable food items in
stomachs of goldeye . . . . . ..
Numbers of major identifiable food items in stomachs
of channel catfish . . . . . . . . . ....•
Numbers of major identifiable food items in stomachs
of,shovelnose sturgeon collected in May and June,
1975 and 1976 ..................•
Numbers of major food items in stomachs of shovelnose
sturgeon collected July through September, 1975 and 1976
163
Page
164
165
166
167
168
169
TABLE F-1. Numbers of major identifiable food items in sauger stomachs.
Total
Length Weight Location Date Ephemeroptera Trichoptera Flathead Sturgeon Longnose iiybognathus Channel Stonecat
(nm) (m) Chub Chub Dace sp. Catfish
Fry
203 77 Intake 9/12/75'
208 41 Intake 9/12/75 7 1
228 82 Intake 9/12/75 27 2
230 95 Miles C. 8/05/76
250 113 Miles C. 8/05/76
250 181 Miles C. 9/10/75 2
255 136 Intake 8/20/75
260 113 Intake 9/12/75 20 1
260 "113 Intake 9/12/75 8 2
263 145 Intake 8/20/75 3
"' 263 154 Intake 8/20/75 2 ....
273 209 Miles C. 9/10/75
278 154 Intake 9/12/75 79
278 227 Miles C. 9/10/75 3
290 181 Miles C. 8/05/76 1
293 204 Miles C. 8/17/76 2
295 191 Miles C. 8/26/76
300 204 Mi 1 es C, 8/05/76
310 200 Miles C. 8/27/75
320 254 Forsyth 10/23/75
360 399 Miles C. 9/l 0/75 2
375 ? Miles C. 1/29/75
450 ? Miles C. l/29/75 3
450 971 Miles C. 8/05/76
TOTALS 143 6 6 4 6 3 11
TABLE F -2. Numbers of major identifiable food items in burbot stomachs collected in January 1976 near Miles ~ity.
Total
Length Weight Ephemeroptera Plecoptera Trichoptera Carp Flathead Sturgeon Hybognathuo Fathead Ca to a tol1t4 s Stonecat
{mm) {g) Chub Chub sp. Minnow sp.
340 290 3
365 227 2
365 236 13
~ 385 295 4
. "' 388 254
U1 405 236 5 1
423 3la 1
430 363 9 3 2
438 408 1 4
465 463 1
480 508 2 2
TOTALS 4 13 9 2 11 8 8
TABLE F-3. Numbers of major identifiable food items in stomachs of goldeye.
Total Misc.
Length Weight Location Date Ephemeroptera Plecoptera Trichoptera Diptera Aquatic Terrestrial
(mrn) (g) Species Insects
2B8 159 Miles C. 8/05/76 3
290 191 Miles C. 8/05/76 1
290 263 Miles C. 8/05/76 1 1 1
293 218 Miles C. 8/05/76 2 8 2
300 200 Miles C. 8/18/75 9 2
303 218 Miles c. 8/05/76 1 1 1
303 249 Miles C. 8/05/76 1
~ 305 200 Miles C. 8/18/75 1 1 14 "' "' 310 318 Miles C. 8/05/76 1
310 354 Miles C. 8/27/75 581 9 1 74
313 249 ? ? 8 3 1
315 245 Miles C. 8/05/76 4 1
315 272 Miles C. 8/05/76 1
318 272 ? ? 5 4
325 318 ? ? 2 2 3
325 318 ? ? 21 2 21
330 354 Miles C. 8/27/75 1 1 1
TOTALS 634 3 27 37 10 87
-
TABLE F-4. Numbers of major identifiable food items in stomachs of channel catfish.
Total
Length Weight Location Date Ephemeroptera Plecoptera Trichoptera Oiptera Terrestrial Fish
(mm) (g) Insects
233 109 Intake 8/21/75 19 18 24
303 204 Miles C. 8/27/75 149 2 81
323 245 Intake 7/22/76 2 8
338 299 Miles C. 8/27/75 1
338 372 Miles C. 8/27/76 1 1
350 ? Miles C. 6/08/76 1 4 63 3 1
3g3 454 Intake 7/22/76 1 35
~ 405 608 Miles c. 8/17/76 536 4
"' 425 644 Miles C. 8/27/75 11 49 ......
433 789 Miles C. 9/10/75 6 1 105
455 962 Miles C. 8/05/76 1993 7
458 1016 Intake 7/22/76 2 11
490 1361 Intake 7/22/76 1 66
500 1297 Miles C. 8/27/75 3 1 1 202
525 1624 Intake 9/12/75 2205 7
565 1588 Intake 7/22/76 1 4 la
578 2014 Intake 9/12/75 g15 5 5
741 4425 Tongue R. 8/27/76 ]b ,,
TOTALS 5830 4 111 123 487 2
a Stonecat
b Shorthead red horse
TABLE F-5. Numbers of major identifiable food items in stomachs of shovelnose sturgeon collected in May and June, 1975 and 1976.
Total Fork
Length Length Weight Location Date Ephemeroptera Plecoptera Trichoptera Diptera Terrestrial
{mm) (mm) (g) Insects
343 308 132 Intake 5/15/75 6 l 2 55
355 325 145 Intake 5/15/75 7 2 5 9
363 330 141 Intake 5/15/75 l 2 3 16
388 350 181 Intake 5/15/75 l 3 l 34
400 390 209 Intake 5/15/75 8 8 30 269
428 390 218 Intake 5/15/75 38 31 104 67
438 398 218 Intake 5/15/75 l l
450 410 240 Intake 5/15/75 46 9 20 11
~ 450 435 272 Intake 5/15/75 ll 31 62 ll "' 0> 478 435 318 Intake 5/15/75 18 92 78 82
480 438 331 Intake 5/15/75 3 20 l
540 485 499 Intake 5/15/75 47 42 192 49
548 495 508 Intake 5/15/75 21 63 82 28
615 573 807 Intake 5/15/75 3 8 22 2
738 668 1216 Intake 5/15/75 30 299 333 18
775 705 1851 Terry 6/16/76 2 5 140 l
785 725 2064 Miles C. 6/02/76 51 16 21 2
850 785 ? Miles C. 6/08/76 1 16 l
875 813 7 Miles C. 6/08/76 5 8 31 2
875 813 3334 Miles C. 6/16/76 140 75 359 15
TOTALS 435 700 1522 673
--
TABLE F-6. Numbers of major food items in stomachs of shovelnose sturgeon collected July through September
1975 and 1976.
Total Fork
Length Length Weight Location Date Ephemeroptera Plecoptera Trichoptera Diptera Terrestrial
(rrrn) (mm) (g) Insects
325 300 100 Intake 8/20/75 43 2 8
343 310 118 Intake 8/20/75 28 1 2
350 313 118 Intake 8/20/75 33 2 61
378 355 240 Intake 8/07/76 13 6 1183
378 348 249 Intake 8/07/76 36 1 2
380 350 136 Intake 8/21/75 40 3 536
380 343 154 Intake 8/20/75 47 4
430 385 227 Intake 8/20/75 93 4 23
~ 453 403 426 Intake 8/07/76 127 8 3
"' 480 450 336 Intake 8/20/75 118 2 6 57 1.0
485 440 299 Intake 8/20/75 93 1 4 23
513 475 404 Sidney 8/30/76 16 4
520 470 390 Intake 8/20/75 151 2 6 71
550 500 735 Intake 7/26/76 44 1 5
553 493 567 Intake 7/26/76 99 1 2
565 513 517 Intake 8/30/76 17 2 30 6
565 513 517 Intake 8/30/76 11 9 164
588 530 762 Intake 8/07/76 113 4 13 16
623 590 907 Intake 9!12/75 69 5 45
733 673 1243 Intake 9/12/75 246 5 15 171
843 770 2268 Intake 8/20/75 1428 4 9 4
TOTALS 2865 17 125 . 2390 7
YELLOWSTONE BASIN FORAGE FISH REPORTED BY BROWN (1971)
Scientific Name
Family Cyprinidae
Notemigonus arysoZeuaas
SemotiZus margarita
SemotiZus atromaauZatus
Phoxinus neogaeus*
Hybopsis graaiZis*
Hybopsia geUda*
Covesius plumbeua*
Notropia atherinoides*
Notropis stramineus*
Hybognathus hankinsoni*
Hybognathus p~itus*
Hybognathus nuahaZua*
Pimephales promeZus*
Rhiniahthys aataraatae*
Family Catostomidae
Catoatomus platyrhynahus*
Family Ictaluridae
Noturus flavus
Common Name
Golden shiner
Pearl dace
Creek chub
Finescale dace*
Flathead chub*
Sturgeon chub*
Lake chub*
Emera 1 d shiner*
Sand shiner*
Brassy minnow*
.Plains minnow*
Silvery minnow*
Fathead minnow*
Longnose dace*
Mountain sucker*
Stonecat
*These species were collected during this study.
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