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Vol. II 


OCTOBER. 1929 


No. 2. 


BULLETIN 

OF 

The New York State College of Forestry 
At Syracuse University 

FRANKLIN MOON. Dean 


Roosevelt Wild Life Annals 

VOLUME 2 NUMBER 2 

OF THE 

Roosevelt Wild Life Forest Experiment Station 


Entered as second-class matter October 18, 1927, at the Post 
Office at Syracuse, N. Y., under the 
Act of August 24, 1912 

[ 147 ] 



Hill 


ANNOUNCEMENT 

The serial publications of the Roosevelt Wild Life Forest Experiment 
Station consist of the following: 

1. Roosevelt Wild Life Bulletin. 

2. Roosevelt Wild Life Annals. 

The Bulletin is intended to include papers of general and popular interest 
on the various phases of forest wild life, and the Annals those of a more technical 
nature or having a less widespread interest. 

These publications are edited in cooperation with the College Committee on 
Publications. 

The editions of these publications are limited and do not permit of general 
free distribution. Exchanges are invited. The subscription price of the Bulletin 
is $4.00 per volume of four numbers, or $1.00 per single number. The price 
of the Annals is $5.00 per volume of four numbers, or $1.25 per single number. 
All communications concerning publications should be addressed to 

The Director and Editor, 

Roosevelt Wild Life Forest Experiment Station, 
Syracuse, New York. 


Copyright, 1929, by 

Roosevelt Wild Life Forest Experiment Station 


[148] 


TRUSTEES OF THE NEW YORK STATE COLLEGE OF FORESTRY 


Ex Officio 

Dr. Charles W. Flint, Chancellor Syracuse University 

Dr. Frank P. Graves, Commissioner of Education Albany, N. Y. 

Hon. Alexander Macdonald, Conservation Commissioner Albany, N. Y. 

Hon. Herbert H. Lehman, Lieutenant-Governor Albany, N.Y. 

Appointed by the Governor 

Hon. John R. Clancy Syracuse, N. Y. 

Hon. Harold D. Cornwall Glenfield, N. Y. 

Hon. George W. Driscoll Syracuse, N. Y. 

Hon. William H. Kelley Syracuse, N. Y. 

Hon. Louis Marshall New York City 

Hon. Edward H. O’Hara Syracuse, N. Y. 

Hon. Charles A. Upson Lockport, N. Y. 

Hon. J. Henry Walters New York City 

Hon. Edmund H. Lewis Syracuse, N. Y. 

Officers of the Board 

Hon. Louis Marshall President 

Hon. John R. Clancy Vice-President 


HONORARY ADVISORY COUNCIL OF THE ROOSEVELT WILD LIFE 

STATION 

American Members 


Mrs. Corinne Roosevelt Robinson New York City 

Hon. Theodore Roosevelt New York City 

Mr. Kermit Roosevelt New York City 

Dr. George Bird Grinnell New York City 

Hon. Gifford Pinchot Milford, Pa. 

Mr. Chauncey J. Hamlin Buffalo, N. Y. 

Dr. George Shiras, 3rd Washington, D. C. 

Dr. Frank M. Chapman New York City 

Dean Henry S. Graves New Haven, Conn. 

European Member 

Viscount Grey Fallodon, England 


ROOSEVELT WILD LIFE STATION STAFF 


Franklin Moon, M.F 


Dean of the College 


Charles E. Johnson, A.M., Ph.D Director of the Station 

Wilford A. Dence, B.S Ichthyologist and Ass’t Director 

Miriam S. Mockford Secretary 


Temporary Appointments * 


Perley M. Silloway, M.S Field Ornithologist 

Aretas A. Saunders, Ph.B Field Ornithologist 

Robert T. Hatt, A.M Field Naturalist 

M. W. Smith, A.B Field Naturalist 

Myron T. Townsend, A.B., Ph.D Field Naturalist 

Charles J. Spiker, A.B Field Naturalist 

Dayton Stoner, Ph.D Field Ornithologist 

Justus F. Muller, Ph.D Field Naturalist 

Harley J. Van Cleave, Ph.D Field Naturalist 

Le Roy C. Stegf.man, M.S Field Naturalist 


Collaborators * 


Richard A. Muttkowski, A.M., Ph.I) Field Naturalist 

Gilbert M. Smith, Ph.D Field Naturalist 


* Including only those who have made field investigations and whose reports are now in 
preparation. 


GENERAL CONTENTS 

PAGE 

1. The Ecology of Trout Streams in Yellowstone National Park. 

Richard A. Muttkowski. 155 

2. The Food of Trout Stream Insects in Yellowstone National Park. 

Richard A. Muttkowski and Gilbert M. Smith. 241 

ILLUSTRATIONS 

FIGURES 

Fig. 53. Yellowstone River above Cooke City bridge. End of “ Lower Canyon ”. August 

8, 1921 154 

Fig. 54. Clearwater River, Idaho, a short distance above the Oro Grande River, showing 
type of shore, stream bed, etc. This region was swept by forest fires in 1915; the 

trees on the slopes are fire-killed. August 30, 1924 154 

Fig. 55- Junction of Yellowstone and Lamar rivers at low water stage. View downstream ; 

Yellowstone River at left, Lamar entering at right. In spring the boulders in 

the foreground are under water. September 5, 1921 159 

Fig. 56. Oro Grande River, Idaho. About 300 yards above its entry into the Clearwater. 

Showing rapids and boulders. In spring all except the largest boulders are 

covered by water. August 31, 1924 159 

Fig. 57. Tower Creek, above the canyon. September 6, 1921 160 

Fig. 58. Slough Creek, showing connected pools. The placid surfaces indicate the pools, 
the riffles indicate the gentle rapids connecting them. Photograph taken just 
above gorge, through which the creek enters the Lamar River. August 11,1921.. 160 

Fig. 59. Slough Creek meadows. August 29, 1921 163 

Fig. 60. Smaller Peak northwest of Lake MacDonald, Glacier National Park, showing the 
beds and confluences of temporary streams. While upper parts are dry, the 

streams still contain water at the confluence. August 10, 1925 163 

Fig. 61. Mt. Brown and others, Glacier National Park. Taken from Lake MacDonald, after 

a summer blizzard. August 15, 1925 164 

Fig. 62. Temporary stream resulting from summer blizzard; photograph taken on mountain 

slope, about 2500 feet above Lake MacDonald, Glacier Park, August 17, 1925 ... . 164 
Fig. 63. Bed of hillside stream (temporary stream), with trickle of water from spring. Sand- 
stone formation, Clearwater River, Idaho. August 30, 1924 167 

Fig. 64. Bed worn in sandstone by temporary stream, Clearwater River, Idaho. Area burnt 

over by forest fire. August 30, 1924 167 

Fig. 65. Lamar River eddy, looking upstream. To the left the high water mark of the spring 
floods shows clearly. In June the stone in foreground was completely covered by 

water. September 4, 1921 168 

Fig. 66. Grand Canyon of the Yellowstone. Lower Falls at upper left. The characteristc 

“ su'phur slides ” to the right. August 21, 1921 168 

Fig. 67. “ Sulphur slides ” of Yellowstone Grand Canyon. Intermixed with these are 
“ needles ”, which also are characteristic of the formations of Yellowstone Park. 

August 21, 1921 171 

Fig. 68. Lower Falls of the Yellowstone and rapids. Note intermixing of “ needles ” and 

“slides”. August 21, 1921 171 

Fig. 69. “ The Needles ”, looking directly across the Yellowstone in the Lower Canyon. 

Note the layer of basalt rocks near the top. August 22, 1921 172 

Fig. 70. Yellowstone River at Cooke City bridge. Lamar River Valley in upper middle. 

August 8, 1921 172 

Fig. 71. Rocks at eddy of Lamar River. Low water stage. In June these were completely 

covered by the floods. September 4, 1921 177 

Fig. 72. Stream bed of Lamar with recession pools. August 8, 1921 177 

Fig. 73. Beaver pond on Lost Creek, showing hut in middle. June 26, 1921 178 

Fig. 74. Lost Creek Falls. September 2, 1921 178 

Fig. 75. Lost Creek, low water stage. In June all the stones were covered by water. Sep- 
tember 2, 1921 1 81 

Fig. 76. Lost Creek, low water stage. Showing the last pool in the bed of the stream. The 

stream is dry for nearly a hundred yards above this point. September 2, 1921 . . 181 

Fig. 77. Tower Creek, confluence with Carnelian Creek (right). September 6, 1921 182 

Fig. 78. Tower Creek in Tower Creek Canyon, showing the thickets along banks and stones 

in bed of stream. August 14, 1921 182 


Roosevelt Wild Life Annals 

PAGE 

Fig. 79. Hot spring on shore of Yellowstone River. Covered in June. August 15, 1921 ... . 187 
Fig. 80. Cleft boulder on meadow between Yellowstone and Lamar rivers. July 17, 1921. . . 187 
Fig. 81. Brink of Lost Creek Canyon to right, and “ crater ” in foreground. The meadows 
are said to be the bottom of the crater, the hills around forming the rim of an 

extinct volcano. August 28, 1921 188 

Fig. 82. Castle Rock (also called Cathedral Rock) on North Fork of Clearwater River, 
Idaho. Showing types of shores and placid stretches of stream. September 2, 

1924 188 

Fig. 83. Clearwater River, Idaho. Showing sand deposits left by spring flood, and log jam 

in river. August 31, 1924 193 

Fig. 84. Clearwater River, Idaho. A closer view of log jam caused by spring flood. Also 

showing “ The Gates ” and government bridge across river. August 31 , 1924. . . . 193 
Fig. 85. Hibernating Coccinellidae. Photograph taken on a warm spring day when sun 
brought out the beetles. Many had been washed into a creek about twenty feet 

away. Photograph Moscow Mt., Idaho, about April 15, 1923 194 

Fig. 86. Skeleton of winter-killed buffalo, near Lamar River eddy. Note the puparia of 
flies on the scapula. The skull had been dragged into the eddy by some animal 

(bear?). July 25, 1921 . 194 

Fig. 87. Huge boulder in stream bed of Oro Grande River, Idaho. This boulder is fully 
forty feet high. Smaller boulder can be seen on the slope along the river. 

September 2, 1924 199 

Fig. 88. Trick Falls, Glacier Park, in Two Medicine River, a short distance below Two 
Medicine Lake. Photograph July 17, 1925. The same place was visited August 
26; the lower part of the falls, which emerges from an underground conduit, was 

then completely dry 199 

Fig. 89. Keppler Cascade, Yellowstone Park. August 18, 1921 200 

Fig. 90. Oro Grande River, Idaho. Freak roots of a tree on top of a boulder. One root 
circles to the left and then turns under the tree. The boulder is surrounded by 
water, and none of the roots passes into the stream bed; the boulder showed no 

sign of being cleft 200 

Fig. 91. MacDonald Creek, Glacier Park. Just above the falls the stream bed consists of 

stratified rock. August 17, 1925 203 

Fig. 92. Yellowstone River at Cooke City bridge. Showing rapids and marginal pools. 

August 15, 1921 203 

Fig. 93. Yellowstone River. Showing rock with “ splash flies ”. July 7, 1921 204 

Fig. 94. Lamar River eddy, showing marginal pools. Later these pools became dry. Pool 
upper left is completely cut off from stream. In the middle the moist bottom of 

a recession pool shows clearly. July 16, 1921 204 

Fig. 95. Yellowstone River, rapids and whirlpool, a short distance above Cooke City bridge, 

July 7, 1921 ' 207 

Fig. 96. Lost Creek, showing tangle and underbrush along stream. September 2, 1921 ... . 207 
Fig. 97. Spider webs, with prey of aquatic insects. From rocks beside Lost Creek Falls. 

September 2, 1921 208 

Fig. 98. Details of a spider web, showing various insect adults. Lost Creek Falls. Sep- 
tember 2, 1921 208 

Fig. 99. Pteronarcys calif ornica nymphs on rocks, “ emerging ” from their nymphal skins. 

July 25, 1921 211 

Fig. 100. Rock with exuviae of Acroneuria. Oro Grande River, Idaho. July 3, 1924 21 1 

Fig. 101. Cluster of Acroneuria adults in crevice of rock. Yellowstone River. July 6, 1921.. 212 
Fig. 102. Stoneflies ( Acroneuria ) mating on shore grass along Yellowstone River. July 

6, 1921 212 

Fig. 103. Adult mayfly with parasitic worm ( Mermis sp. ?) emerging from the caudal end. 

Enlarged times eight. Note the loop formed by the parasite within the abdomen 
of the insect. From confluence of Lava Creek and Gardiner River, August 4, 1921. 217 
Fig. 104. Stranded caddis worms {Brachycentrus and Rhyacophila). Lamar River. August 

8, 1921 217 

Fig. 105. Attachment of Brachycentrus cases. Some attached at caudal or small end, others 

at broad or “ mouth ” end. Lamar River. July 25, 1921 218 

Fig. 106. Larva of Bibiocephala, enlarged times 6. Note ventral suckers. From Snake 
River, Idaho. At right, pupae of Bibiocephala, showing variation in size and 

ventral attachments 218 

Fig. 107. Bibiocephala pupae. From Lamar River. Note the tubes of Chironomids ( Tany - 

tarsus ?) on the same rock. July 16, 1921 219 

Fig. 108. Bibiocephala adults as “ splash flies ”. Oro Grande River, Idaho. September 

3 , 1924 2I 9 

Fig. 109. Deuterophlebia larva. Yellowstone River. July 30, 1921 220 

Fig. no. Simulium sp. “ Combs ” of larva x 60 220 


Ecology of Trout Streams 


PAGE 

Fig. hi. Atherix cluster. Lamar River, July 22, 1921. The insert shows a section of the 

cluster enlarged about x 4 225 

Fig. 1 12. Rock where Atherix cluster had formed, on underside in cleft of rock. Lamar River, 
August 7, 1921. On July 22, when the cluster was photographed, the sharp edge 

running from left to right was about twelve inches above the rapids 225 

Fig. 1 13. Tipulid larva, with inflated “ baloon” at posterior end. Tower Creek, August 29, 

1921 226 

Fig. 1 14. “Spray flies” ( Chamaedipsis and Philolutra) on rock in rapids. Lamar River, 

August 31, 1921 226 

Fig. 1 15. Pamidae larva. Psepkenus leconlei enlarged x 10. From Lake Mendota, Wis. .. . 232 
Fig. 1 16. Pamidae larva. Elmis viltatus enlarged x 10. From Lake Mendota, Wis 232 


[i53] 



Fig- 53 - Yellowstone River above Cooke City bridge. End of “Lower Canyon.” 

Aug. 8, 1921. 



Fig. 54. Clearwater River. Idaho, a short distance above mouth of Oro Grande 
River, showing type of shore, stream bed, etc. This region was swept by forest 
fires in 1915; the trees on the slopes are fire-killed. Aug. 30, 1924. 


[ 154 ] 






THE ECOLOGY OF TROUT STREAMS IN YELLOWSTONE 

NATIONAL PARK 

By Richard A. Muttkowski* 

Collaborator, Roosevelt Field Naturalist, Roosevelt Wild Life 
Forest Experiment Station, Syracuse, Nezv York 

CONTENTS 

PAGE 

Introduction 156 

Mountain Trout Streams 158 

Classification of Mountain Trout Streams 158 

Description of the Type Streams 161 

Criteria of Mountain Stream Life 166 

Stream Physiography 166 

Stream Physiology 174 

Qualitative List of Plants and Animals 179 

Plants 179 

Animals 180 

Ecology of Mountain Trout Streams 206 

General 206 

Classification of Habitats 209 

The Habitats 210 

Adaptations to Mountain Stream Life 221 

Food Relations 222 

Trout Food 222 

Insect Food 230 

Seasonal Food Cycle 233 

Comparisons and Summaries 234 

Bibliography 238 


* Professor of Biology and Head of the Department of Biology, University of Detroit, 
Detroit, Michigan. 


Roosevelt Wild Life Annals 


is6 


INTRODUCTION 

Under the auspices of the Roosevelt Wild Life Forest Experiment Station 
at the New York State College of Forestry, Syracuse, N. Y., the writer was 
afforded an opportunity during the summer of 1921 to examine and study trout 
streams in the northwestern section of Yellowstone National Park. Camp 
Roosevelt, operated by the Yellowstone Park Camps Company, was the base 
from which these studies were made, covering the period from June 18 to 
September 9, inclusive. 

Due to unforeseen complications, chiefly in the way of health and change of 
position, the completion of the manuscript was delayed till 1927. In the mean- 
time the writer has had ample opportunity to study other mountain streams in 
a comparative way in Idaho, Washington and Montana. Chief among these are 
the Palouse, Clearwater, Oro Grande, Snake, and St. Joe rivers in Idaho and 
Washington; and the streams comprising the MacDonald drainage, Two Medicine 
drainage, St. Mary’s drainage and Swift Current drainage in Glacier National 
Park in Montana. The Glacier Park studies were made during the summer of 
1925 and included a number of lakes and streams. The results as far as the 
lakes of Glacier Park are concerned are to be published in a separate paper. 
Data pertaining to streams are, however, incorporated in the present paper rather 
than in a separate account. 

Acknowledgments. In Yellowstone Park the writer was variously aided 
by different persons, notably Dr. Gilbert M. Smith of the University of Wiscon- 
sin, and more recently of Stanford University (see collaboration, Muttkowski- 
Smith, the Food of Trout Stream Insects in Yellowstone National Park, in the 
Roosevelt Wild Life Annals, Vol. 2, No. 2), Mr. Alvin G. Whitney of the 
Yellowstone Park Forest and Trail Camp, Mr. E. R. Warren of Colorado 
Springs, Colo., and his assistant Mr. Ellis L. Spackman. Mr. Horace M. Albright, 
the Superintendent, facilitated the work by granting certain special permissions. 
Mr. M. P. Skinner, then Park Naturalist, and the rangers of the Tower Fall 
Junction Ranger Station assisted in various practical ways and by suggestions 
as to favorable localities. Above all, I am indebted to Dr. Charles C. Adams, 
until recently Director of the Roosevelt Wild Life Forest Experiment Station 
for many suggestions and direct aid; and to Mr. Howard H. Hays, then President 
of the Yellowstone Park Camps Company, for many courtesies, conveniences, and 
facilities, without which this study would hardly have been possible. To the present 
staff of the Roosevelt Station I am indebted for the laborious task of preparing this 
paper for the press and seeing it through. 

To the Zoological staff of Cornell University I am indebted for identifica- 
tions of various specimens: Dr. Needham and Dr. A. Claassen identified the 
Perloidea, Dr. Needham the Ephemeroidea, Mr. C. K. Sibley the Trichoptera, 


Ecology of Trout Streams 


x 57 


Dr. A. O. Johannsen the Diptera, and Mr. H. Dietrich the Coleoptera. Most of 
the insects were in the nymphal or larval stages and the task of identification was 
therefore none too easy. To all these specialists I wish to express my grateful 
acknowledgment. 

In general, the plan of the present paper follows that of an earlier one, 
the Fauna of Lake Mendota (Muttkowski, T8). That plan has received the 
sanction and approval of a number of ecologists, so that I do not hestitate to 
repeat it in the present study although slightly modified. 


158 


Roosevelt Wild Life Annals 


MOUNTAIN TROUT STREAMS 

Classification of Mountain Trout Streams. Trout streams are highly 
aerated streams, found most abundantly in mountain regions. In the plains there 
are many “meadow” streams which also contain trout. These, however, are 
only of secondary interest here, since they are rare in mountainous regions. 

Trout streams in Yellowstone Park and elsewhere in the Northwest can be 
broadly classified into three groups, according to certain physical characters : 

a. Constant streams, with large amounts of water, which are, relatively speak- 
ing, only slightly diminished in summer. This group comprises the larger streams, 
such as Yellowstone River (Fig. 53), Gibbon and Firehole rivers in Yellowstone 
Park; the Snake, Boise, Clearwater (Fig. 54), Salmon, Coeur d'Alene and other 
larger rivers of Idaho; the Flathead and St. Mary’s rivers in Glacier Park. 

b. Variable or flood streams, which carry enormous masses of water for 
brief periods in the spring, due to melting snow, and then rapidly recede to one 
tenth or less of their flood level. These streams contain many rapids and in 
flood period may attain a formidable size. As examples may be mentioned the 
Lamar (Fig. 55), Gardiner, and Firehole rivers in Yellowstone Park, the forks 
of the Elk and Clearwater rivers and the Oro Grande (Fig. 56) and Palouse 
in Idaho and Washington, the Two Medicine River, MacDonald Creek and 
Swiftwater Creek in Glacier Park. 

c. Precipitous or cascading streams, with many falls and rapids. Like the 
foregoing they are raging torrents during a brief spring, after which they shrink 
to unimpressive proportions, indeed, often to little more than mere trickles. This 
type is abundant throughout the Rockies. For the Yellowstone Park. I may 
cite Soda Butte Creek, Deep Creek, Broad Creek, Hellroaring Creek, Lava Creek, 
Lost Creek, etc. Tower Creek (Fig. 57) is an intermediate between b and c. but 
faunistically like c. 

Yellowstone Park contains another stream which is unique and the sole 
representative of its type. This is Slough Creek, which consists of several 
tiers of meanders, and is located in the northeast corner of the Park (Fig- 58 ). 
There one finds splendid meadows, several miles in length, through which the 
stream meanders placidly (Fig. 59). The stream leaps from one meadow to 
the next through short hut magnificent gorges. But the chief characteristic 
of the stream is probably glacial in origin ; for the meanders consist of a series 
of deep holes, lined with huge boulders, which are connected by the quietly flow- 
ing stream. The rapids are confined to the gorges. In the “holes" or quiet pools 
one finds some of the largest trout in the Park. 

Other mountain streams may course through long meadows and form 
meanders ; but the “holes" are only occasional and do not consist of a series of 
depressions such as one finds in Slough Creek. 

d. Temporary streams, or snow flood streams. These are not trout streams 
at all, but are included on account of their physical rather than biological rela- 
tionship. This type includes the precipitous cascades and trickles that arise from 
melting snows and which for a time may carry considerable quantities of water, 
but which diminish to weak rills by the middle of summer and freeze up com- 


159 



Fig. 55. Junction of Yellowstone and Lamar rivers at low water stage. View 
downstream; Yellowstone River at left, Lamar entering at right. In spring 
the boulders in the foreground are under water. Sept. 5, 1921. 



Fig. 56. Oro Grande River, Idaho. About 300 yards above it's entry into the Clear- 
water. Showing rapids and boulders. In spring all except the largest boulders 
are covered by water. Aug. 31, 1924. 



i6o 




Fig. 58. Slough Creek, showing connected pools. The placid surfaces indicate 
the pools, the riffles indicate the gentle rapids connecting them. Photograph 
taken just above gorge, through which the creek enters the Lamar River. 
Aug. 11, 1921. 


Ecology of Trout Streams 


161 


pletely in the fall (Fig. 60). Snowstorms and summer blizzards may give these 
streams a temporary prominence (Fig. 61). They become conspicuous as the 
snow melts, and the noise of their torrential fall can be heard at great distances 
(Figs. 62, 63, 64). Quite generally they end in sumps or swamps on the moun- 
tain sides or at the base of the slopes. Despite their temporary existence they 
have a fauna and a flora ; and their terminal sumps supply abundant habitats 
for the early summer plagues of mosquitoes so common in mountain regions. 

In selecting streams for comparative study it was essential to consider 
local convenience, accessibility, and type of stream. Four were selected for 
their location near Camp Roosevelt, which was used as a base. It would be 
difficult to find another point in the Park so favorably located, with repre- 
sentative types of so many kinds of streams all within convenient walking 
distance. After a preliminary survey, the following were chosen for intensive 
study: Yellowstone River, Lamar River, Tower Creek, and Lost Creek. 

Yellowstone River was chosen to represent the first type, the large “con- 
stant” stream. The river is less than a mile distant from Camp Roosevelt and 
offers many ideal habitats on both sides of the Cooke City Road bridge, within 
convenient distance. 

Lamar River was selected to represent the second type, the variable or 
flood stream. The Lamar joins the Yellowstone about three miles from Camp 
Roosevelt, and about a mile below the Yellowstone bridge. Excellent habitats 
were found in the gorge and eddies (Fig. 65) within the first few miles above 
the junction. 

Lost Creek, although containing no fish at all, was selected for its accessi- 
bility and to represent the cascading or precipitous type of stream. It passes 
right through Camp Roosevelt, and its biota typifies such streams as Lava Creek, 
Tower Creek, Buffalo Creek, Blacktail Deer Creek, Hellroaring Creek, etc. 
Care was taken to check up Lost Creek frequently with Tower Creek, the fourth 
stream. 

Tower Creek at Tower Fall is about two miles distant from Camp Roosevelt. 
But since it is much frequented by campers for about three miles above the 
mouth, the distance to the undisturbed sections made it rather inconvenient 
for frequent study. Besides, Lost Creek, as already noted, showed a practical 
identity of biota; hence one trip a week was considered sufficient for the study 
of Tower Creek. 

The fauna of each type showed marked individuality. The work of com- 
parison was begun at a favorable period, just preceding the summer emergence 
or transformation of insect forms. This seems to follow shortly after the spring 
flood period. Later on, after the first six weeks, as opportunity offered, hurried 
studies were made of other streams for comparison, such as the Gardiner and 
Firehole rivers, Lava Creek, Blacktail Deer Creek, Carnelian Creek, Elk Creek, 
Pelican Creek, Plateau Creek, and Buffalo Creek on the Lamar and Yellowstone 
rivers. Three days were also spent in a study of the biota of Yellowstone Lake, 
particularly in its relation to Yellowstone River. 

Description of the Type Streams, a. Yellowstone River. The Yellowstone 
River arises far south of Yellowstone Lake. For the purpose of this paper only 


Roosevelt Wild Life Annals 


162 

the stretches below the lake are considered. After leaving the lake, the river 
is rather broad and in numerous places tends to become shallow and swampy, 
particularly on the right shore. Notwithstanding the swift current, considerable 
vegetation is present, such as Myriophyllnm, Ceratophyllnm, some Potamogeton, 
and the plumes of algae (probably Cladophora) . This is confined to the lateral, 
quite shallow portions of the stream. In the adjacent swamps Castalia, N ymphaea 
and other swamp plants attempt to invade the stream, with little success. 

About a mile above the Upper Falls the current increases its speed and 
plants become very rare, except Cladophora, which persists nearly to the 
brink of the falls. Just below the mouth of Alum Creek the river bed narrows 
and the shores become higher and steeper. The water, till then smooth and 
silent, now becomes turbulent, noisy and streaked with foam. Entering a short, 
rocky canyon, the river leaps over the brink with a vertical drop of 109 feet, 
forming the Upper Fall. 

Here the aspect of the shores changes. For the Grand Canyon has begun, 
with its multitude of colors, its precipitous “needles” and rocks, its gav slides 
of sulphur sands — all thrown together in fantastic design. For twenty miles 
the canyon extends, with alternating areas of strangely colored formations and 
bluish gray cliffs (Figs. 66 and 67). 

A third of a mile below the Upper Fall, the river takes a second leap of 
308 feet, the Lower Fall (Fig. 68). The river then plunges into a series of 
cataracts, rapids and lesser falls, for a distance of twenty miles, or the length 
of the Grand Canyon. The total descent from Yellowstone Lake to this point 
is from 7740 to 6400 feet elevation. 

A short distance above Tower Fall the canyon flattens out and the river 
becomes more placid. Tower Creek marks the entry into the Lower Canyon 
(“The Needles.” Fig. 69). Here the shores are formed of steep, blue-grav 
cliffs, interspersed with minor slides of gayly colored sulphur sands. Below 
this is the Cooke City Road bridge (Fig. 70). Beyond the bridge the river is a 
series of rapids and eddies, winding between low and high hills, with occasional 
gorges and short canyons. 

The sound of the river is a dull roar. If one approaches it — be it on a 
low shore, or between high cliffs — one may feel quakes and tremors of varying 
violence, giving one a curious feeling of uncertainty. Combined with this is 
the stench of the river, of sulfuretted hydrogen, like foul eggs, due to the masses 
of sulphur carried, and still more to the innumerable hot springs, small geysers, 
and mud swamps along the shores. The sulfuretted odor and taste of the water 
is never quite absent from the river; indeed, fish taken from the Yellowstone 
River have a strongly sulphurous taste. 

b. Lamar River. The Lamar River drains practically the entire northeastern 
section of Yellowstone Park. More specifically, to the west and south it drains 
the watershed between the Lamar and Yellowstone rivers and Y'ellowstone 
Lake. To the east, it collects the waters from the Absaroka Range. For the 
greater part it flows northwest, its bed lying in a basin between the foothills of 
the Absarokas to the east, Specimen Ridge and Mirror Plateau to the west, and 
a series of peaks to the south, including Pelican Cone, Mt. Chittenden, Cathedral 
Peak, and Pyramid Peak. 


163 




Fig. 60. Smaller Peak northwest of Lake MacDonald, Glacier National Park, show- 
ing the beds and confluence of temporary streams. While upper parts are dry, 
the streams still contain water at the confluence. Aug. 16, 1925. 


164 




Fig. 62. Temporary stream resulting from summer blizzard; photograph taken 
on mountain slope, about 2500 feet above Lake MacDonald. Glacier Park, 
Aug. 1 7, 1925. 





Ecology of Trout Streams 


165 

In its northward course it is joined by dozens of rills and creeks. Thus, 
on the left it receives Cold Creek, Willow, Timothy, Clover, Flint, Opal, 
Amethyst, Jasper and Crystal creeks ; on its right it receives Miller, Calfee, 
Cache, Soda Butte and Slough creeks. Of these, Slough Creek and Soda Butte 
Creek are the most important tributaries. 

Lamar River has no conspicuous falls or cascades, but drops steadily and 
gently from 7500 feet elevation at its point of entry into Yellowstone Park to 
5800 feet at its junction with the Yellowstone. It is a beautiful stream, never 
very wide, with alternating placid stretches and gentle rapids. At points where 
tributaries enter, it widens and becomes turbulent, since most of the tributaries 
are precipitous and the force of their waters impound those of the Lamar, 
causing eddies, lateral gorges, and roaring rapids. 

During the spring flood the Lamar rises to formidable heights. On June 
20, 1921, the flood waters covered the rocks shown in figure 71 (see also Fig. 
55). Examination of stranded debris indicated that the waters had been 
several feet higher during the preceding week. Even then the river was 

spectacular, both in appearance and sound — so much so, that as one stood on the 
point above its junction with the Yellowstone, the question suggested itself, 
“Does the Lamar feed the Yellowstone, or the Yellowstone the Lamar?” The 
Lamar seemed to carry a greater volume of water at the time. 

A few days later, June 25, the river had fallen considerably, the boulders 
noted in figure 71 being wholly exposed. By July 16 the stream had fallen to 
the level noted in the photograph. The total drop was approximately fifteen 
feet. 

Following the quick recession of waters, the Lamar forms an ideal habitat 
for Cladophora; the whole river bed is covered with the green streamers, so that 
from an elevated point some hundred feet away the waters appear a brilliant 
green. With the recession a very marked silting occurs in the shallower places, 
which has a striking effect on the stream life (Fig. 72). 

c. Lost Creek. This is a typical mountain creek, carrying large quantities 
of water for short periods, and gradually shrinking to an unimpressive trickle, 
with perhaps less than one-fifteenth of its flood volume. Its main drainage 
is from the northern slope of Folsom Peak. Its banks are, on the whole, steep 
but not high. Smaller beaver works (Fig. 73) occur for six miles above Camp 
Roosevelt. There a series of small pools is connected by trickles, with beaver 
dams impounding the scant waters. 

Lost Creek is not a trout stream, but its fauna and flora are typical of the 
smaller trout streams. For a short distance above its falls it becomes quite 
precipitous. It enters a short gorge, then tumbles over a cliff about sixty feet into 
Lost Creek Canyon (Fig. 74). Its bed then comprises shattered rocks, and some 
fair-sized boulders (Fig. 75). Over these it rushes in a series of steep cascades. 
At the base of the hill it spreads out in a delta and then disappears (Fig. 76) 
into the ground for several hundred yards — hence the name “Lost” Creek. It 
reappears along the Cooke City Road, which it parallels for about 500 yards 
down to Yellowstone River. Here it flows over a series of shelves, which in 
1921 formed the site of a beaver colony, which was abandoned in 1922. 


1 66 


Roosevelt Wild Life Annals 


d. Tower Creek. This creek drains the elevated plateaus between Mt. Wash- 
burn and Folsom and Observation peaks, with headwaters arising at an altitude of 
about 10,000 feet. In its course of about twenty miles it drops to 6400 feet at 
Tower Fall, just before it empties into Yellowstone River. 

In general Tower Creek is about twenty feet wide, and sixteen to twenty- 
four inches deep, with clear, cold water. Its bed is composed of water-worn 
cobbles, from a few inches to a foot in diameter, with occasional larger stones 
or boulders five to ten feet in diameter. In its upper reaches the banks are flat 
and frequently spread out to form broad pastures and willow swamps (Fig. 57), 
with adjacent beaver works built around pools or springs. But the stream itself 
is unobstructed, although frequent attempts at damming are evident. In its 
course Tower Creek receives the drainage waters of innumerable springs, pools 
and swamps, as well as of hillside sumps. 

About seven miles above its mouth it receives the waters of Carnelian Creek 
(Fig. 77), a narrow and shallow stream with considerable fall, which is used 
extensively by beavers for a series of remarkable works (See Roosevelt Wild 
Life Bulletin, Vol. 1, No. 2, pp. 187-221, and Roosevelt Wild Life Annals, Yol. 1, 
Nos. 1 and 2, pp. 13-191, for E. R. Warren’s papers on the Yellowstone Beaver). 
Two miles farther downstream the hills approach each other, and the creek 
enters Tower Canyon, throtigh which it threads for about five miles (Fig. 78), 
emerging in a short gulch which parallels the highway. Here the bed is strewn 
with large rocks, up to ten feet in diameter, over which the water cascades in a 
series of short, turbulent leaps. The gulch continues for approximately 150 
yards, then twists sharply, and ends between the characteristic needles which 
mark the entrance to the Lower Canyon of the Yellowstone. There the creek 
plunges over the cliff for a fall of 132 feet, and after a turbulent passage of 
100 yards, joins the Yellowstone. 

CRITERIA OF MOUNTAIN STREAM LIFE 

The biota of any environment is determined by physiographical and physio- 
logical conditions. Physiography deals with the structural aspects of the envi- 
ronment, physiology with the functional aspects. For the first of these there 
are two viewpoints : — that of the geologist who deals with topographical classi- 
fications, and that of the ecologist who classifies the environment in terms of 
habitats. Hence under Physiography both the topography and ecology of streams 
must be discussed. 

Stream Physiography. The Physical Environment. Under this head the 
sources of the streams and the structure of the shores and stream beds can be 
considered. 

Sources. The sources of water are primarily the melting ice and snows 
of the mountains, and secondly the innumerable hot (Fig. 79) and cold springs 
found in the Northwest. Besides these, many swamps, sumps, and ponds drain 
into the streams. 

The Shores. Geologically Yellowstone Park is of mixed origin — igneous, 
volcanic, glacial and alluvial. This is shown in the character of the various shores 


1 67 



Fig'. 63. Bed of hillside stream (temporary stream), 
with trickle of water from spring. Sandstone forma- 
tion, Clearwater River, Idaho. Aug. 30, 1924. 



Fig. 64. Bed worn in sandstone by temporary stream, Clearwater 
River, Idaho. Area burnt over by forest fire. Aug. 30, 1924. 





i68 



Fig. 65. Lamar River eddy, looking upstream. To the left the high water mark of 
the spring floods shows clearly. In June the stone in foreground was completely 
covered by water. Sept. 4, 1921. 



Fig. 66. Grand Canyon of the Yellowstone. Lower 
Falls at upper left. The characteristic “sulphur 
slides” to the right. Aug. 21, 1921. 



Ecology of Trout Streams 169 

and streambeds. Nearly every stream in the Park at some point or other passes 
through rugged canyons composed of basalt cliffs. Decomposed lava slides are 
frequent. Along the streams and on the uplands one finds numerous boulders 
left by glaciers (Figs. 80 and 87), while in places there are great accumulations 
of soil left by past floods. Much of the area in the region of Camp Roosevelt 
is thought to be the crater of a huge extinct volcano (Fig. 81). 

A feature of the shores of mountain streams is the changes taking place, 
produced by two factors, (a) snow, and (b) the streams. The changes are 
slow but they are nevertheless easily recognizable. The streams for the greater 
part have eroded their beds considerably, so that the present shores are quite 
steep, even perpendicular in many places (Fig. 82). During the spring floods 
the present shores are undermined ; this tends to produce land slides, which in 
turn, precipitated into the waters, affect the stream beds. 

On the steep slopes the long winters deposit gigantic snow drifts, whose 
weight, pressing on trees, bushes and the loose earth, dislodges these and grad- 
ually forces them into the stream. During spring the melting snows may cause 
great sections of the shore slopes to slip into the stream. This is particularly 
true of Yellowstone River, where the slides are numerous, and the shores for 
many miles are quite declivitous (Figs. 66-68). It is also true for streams 
like the Lamar, Tower Creek, Lost Creek and many others. At many points 
along' these streams there were signs of recent “slips” during the summer of 1921, 
and of others of older date. 

In places the trees, shrubbery, and debris thus precipitated into the stream 
may become caught between or against protruding rocks and cause a damming 
of the stream. Jammed trees are frequent in the great rapids of western streams 
(Figs. 83 and 84). 

Wintering animals, such as the Coccinellidae (Fig. 85), may be buried under 
the snow and later swept into the water by the snow slides. Others, including 
mammals such as buffalo, deer and elk, may become mired in the snow-drifts 
and are suffocated (Fig. 86) ; these, too, may be carried into streams by snow 
slides, since quite frequently one may find parts or whole skeletons of winter 
killed mammals in the streams. 

The Stream Beds. Change, too, takes place in the stream beds. The 
force of the spring waters in particular brings about many marked annual 
changes. The flood currents wash out all the lighter materials such as sand, 
mud, silt, and deposits on rocks, so that the bottoms appear clean-washed or 
scoured. Later with the recession of the floods, muck, silt, smaller pebbles and 
sand are deposited along the shores among the rocks. 

In midstream the floods tend to fill up the pools. In turn, they may wash 
out new pools. Even during the summer, with water at lowest stage, and 
depending somewhat on the size of the stream, there is a constant movement of 
the bottom. Stones of varying size are displaced, ground together or battered 
against each other, and whatever living creatures may come between will be 
crushed. A water net, or still better, a plankton net, left in a stream just below 
some rapids, will collect abundant evidence of this fact in the way of crushed 
caddisworms, mayfly and stonefly nymphs, and occasional trout eggs and embryos. 


i yo 


Roosevelt Wild Life Annals 


The Ecological Habitats. Like other ecological units, the mountain stream 
may he subdivided into minor habitats, which can be readily recognized accord- 
ing to physical characters and the biota. These habitats intergrade, here as 
elsewhere. Following is a classification, based on comparative studies of the 
streams of Yellowstone Park and other regions of the Northwest: 

1. Permanent habitats, with native (endemic) biota. 

a. White water habitats — falls, cascades, white rapids. 

b. Clear rapids and stone bottoms — on and under rocks. 

c. Placid water habitats- — pools and holes. 

d. Marginal areas — on or under rocks, in soil. 

2. Interrupted habitats, with native biota. 

e. Deposits— on rocks, bottoms, or shores. 

f. Splash areas — on rocks. 

3. Temporary habitats — transient and transitional, with varied biota. 

g. Marginal pools. 

h. Recession areas. 

The permanent habitats ( 1 ) are stable and are typical of the center of the 
streams; their plant and animal life varies but slightly the year round. 

Interrupted habitats (2) are found both in the center and at the sides. The 
transient and transitional habitats (3) comprise relatively quiet spots, temporary 
in existence, that dry up in low water stage and are destroyed by high water. 
The biota in such areas is extremely varied. 

Permanent habitats. As already noted, these comprise the central parts 
of streams ; they offer the greatest degree of constancy in mountain streams. 
In such places one may find the same fauna and flora practically the year round. 

a. White water habitats. As indicated by the name, these are character- 
ized by foaming or “white” water. That is, here the current and the mass of 
w r ater are sufficiently swdft and great and the obstacles opposed to its flow 
sufficiently firm to batter it into a white foam. Such white water is that of 
falls, cascades, and major rapids. Falls (Figs. 66, 68, 74, and 88) indicate a 
vertical flow of water; cascades an oblique flow (Fig. 89); white rapids (Fig. 
95) are a mixture of horizontal, oblique and vertical currents. In mountain 
streams all of these are intermingled. They constitute a highly specialized 
habitat, combining strong and twisting currents and highest aeration. 

b. Clear rapids and stone bottoms. Here are included rapids of less 
violence, with fewer opposed obstacles, so that the water is transparent and 
one may readily see the bottom. Very characteristically the bottom in these 
rapids is nearly uniformly composed of rounded stones of various sizes (Figs. 
87 and 90). But there may also be angular granitic rocks, and angular strati- 
fied rocks (Fig. 91). Thus, in the Yellowstone, all types of bottom may be 
found. At one point, just below the largest group of “needles" in the lower 
canyon, there is evidence of a formation similar to those of Mammoth Hot 
Springs ; this formation tips into the stream and extrudes at low water stage. 
But the most common condition, which applies probably to more than 90 per 
cent of the stream beds, is that of rounded, water-worn cobbles (Fig. 57). 



Fig. 67. “Sulphur slides” of Yellowstone Grand Canyon. Intermixed with these 
are “needles,” which also are characteristic of the formations of Yellowstone 
Park. Aug. 21, '.921. 



Fig. 68. Lower Falls of the Yellowstone and rapids. 
Note intermixing of “needles” and “slides.” 
Aug. 2i, 1921. 




172 



Fig. 69. “The Needles,” looking directly across the Yellowstone in the Lower 
Canyon. Note the layer of basalt rocks near the top. Aug. 22, 1921. 



Fig. 70. Yellowstone River at Cooke City bridge. Lamar River Valley in upper 

middle. Aug. 8, 1921. 




Ecology of Trout Streams 


i/3 


c. Placid water habitats. These are the “holes” and “pools” in the beds 
of the streams and are of varying size. They may have been washed out by falls, 
gouged out by stones born along by the waters, or they may be of glacial, 
volcanic, or perhaps seismic origin. At the base of falls the pools are turbu- 
lent and belong to the “white water” habitats; otherwise they are relatively 
quiet at the bottom, since the current is strong only in the surface strata. 
Often such pools have a scanty floor of gravel, or a sandy bottom — deposits 
that have been made after the spring floods. 

d. Marginal areas. The shores may comprise cliffs, boulders, or smaller 
stones, and are rarely sand, pebbles, and mud. Here the impact of the water is 
primarily lateral, not horizontal or vertical (Fig. 92). Friction by debris is 
marked. This is an area offering many shelters, but too often of only tem- 
porary nature. Many smaller organisms live under and between the rocks, while 
others live in the moist or wet soil. 

Interrupted habitats. These comprise primarily the deposits (e) on 
the bottoms, shores, and sub-surface rocks. At first these were regarded as 
transient in nature, since the deposits are absent during the flood period and 
accumulate progressively during the summer. Still, one finds these deposits 
in mid-stream, often exposed to a fairly strong current, and covering the huge 
rocks that so often form the margin of the “holes” and pools. The deposits 
persist during the winter and only the scouring spring floods sweep them away. 
But during their existence they afford a habitat for numerous Chironomidae 
and rock diatoms. The deposits extend from mid-stream to the shore rocks. 
In Yellowstone Park they contain much sulphur sand. 

f. Splash areas. These are the exposed rocks in rapids or along shores, 
which are continually moistened by spray. Almost any time during the year — 
spring, summer, fall, winter — one may find adult insects running up the rocks, 
flying into the spray, and once more running upward. They may be found 
chiefly on the downstream side of the rocks. Such are the Diptera, Trichoptera, 
and more rarely the mayflies (Figs. 93, 108 and 114). 

Temporary piabitats. These comprise (g) the marginal pools and shallows 
which are found during a large part of the year, and (h) the recession areas, 
following the spring flood. One might also refer to them as transitional and 
transient areas ; — transitional as regards the biota, transient as regards their 
period of existence. They are the lesser shore rapids, which silt in quickly, 
and the marginal pools that appear with the recession of the flood waters. 
Later on the interstices between the stones become filled in with sand and 
debris (Fig. 94). Tiny rapids or trickles continue to fill in the connections, 
until the pools are completely separated. Often a series of marginal pools is 
thus formed. The trapped fauna either migrates or dies, and the temporary 
habitat becomes populated with invading biota. It is remarkable how quickly 
such a temporary habitat is invaded by aquatic beetles, water bugs, Chiro- 
nomidae, Rotifera, Protozoa, filamentous algae, and scattering plankton ’Crustacea. 
All of these types come primarily from the swamps, sumps, pools, and springs 
found so abundantly in mountain areas. After a few weeks these places dry 


W4 


Roosevelt Wild Life Annals 


up and with them the biota disappears. Or, if a pool is fairly deep and does not 
dry up completely, then the fall rise of the waters will wash away the invading 
hiota and restock the pool with native forms. 

Habitat Distribution. A striking difference between mountain streams and 
other water bodies such as lakes, ponds, and slow plains streams, is the absence 
of regularity in the arrangement of habitats. In mountain streams the 
habitats are all commingled; pools may follow falls, rapids alternate with eddies, 
marginal pools may adjoin cataracts. In other words, there is a complete 
absence of that regularity which permits a zonal classification for lakes, ponds, 
and slow streams. On the contrary, the contrasts are quick and startling, one 
extreme follows another. Hence in a very small area one may find all the 
extremes from a vertical to a horizontal flow of water, from shallow, placid 
stretches to deep, stone-lined pools. This, in a sense, is advantageous, since it 
permits the study of diverse conditions in a rather short time. A second advant- 
age arises from this, namely, that the deeper portions of the stream approxi- 
mate the flood conditions, while shallower places permit more intensive study 
of the biota and its relation to other communities. 

In summary, there is in mountain streams only a horizontal distribution 
of habitats, no vertical. The habitats must be studied in horizontal order, not 
in the vertical order one finds in lakes and slow streams. 

Stream Physiology. From a physical viewpoint, mountain streams are 
distinctive. Parallel with this is the functional or physiological aspect, with 
equally distinctive features, which depend upon extrinsic and intrinsic factors. 
The extrinsic factors are such as affect the stream as an entity, namely, the 
molar agents, including winds and currents, chemical makeup, temperature, and 
circulation. Intrinsic factors are those which affect the makeup of the flora 
and the fauna. These are currents, respiration, food supply, footholds, 
locomotion, and special habits. 

Extrinsic Factors. Molar Agents (Winds and Currents). — Winds do 
not directly affect the mountain streams. Since the streams have bitten and 
scoured their beds deeply, the shores are usually high and the waters are there- 
fore sheltered from winds. The rush of the waters, however, generates definite 
air currents (Fig. 95) which entangle with the shore-winds high above them 
and create vortices and treacherous back drafts which readily draw unwary 
insects and other winged life from their line of flight and spill them into the 
hurrying waters beneath. This results in the surface toll or “surface bait" of 
the summer months. 

In the winter the surface winds carry snow into the gorges and canyons, 
piling it on the shores of their streams in huge drifts, to be dislodged by wind 
vortices or undermined from beneath. Avalanche after avalanche then crashes 
down the slopes, dislodging trees, boulders, or causing huge land slides into the 
streams. In the spring the melting snows are readily displaced by the winds and 
slide into the streams. For weeks after the snow has disappeared from the lower 
levels the streams are turbid from the sands and sediments washed along by the 
currents. 


Ecology of Trout Streams 


175 


To a lesser extent the currents, especially during the flood periods, under- 
mine the shores and cause slides. For it is noteworthy that most slides start 
from above and not from below. 

Specifically, the currents are concerned with molding the bed of the stream, 
the winds primarily with molding the shores (Fig. 96). 

Chemical Composition. In general, mountain streams are noted for the 
purity of their water. This is true also for the streams of Yellowstone Park, 
except Yellowstone River and Firehole River. These two streams are both 
distinguished by a sulphury taste and odor the year round, rendering the water 
unpalatable and incapable of quenching thirst. Two factors seem to 
cause this: (a) The nature of the river shores and bottoms, from which masses 
of sulphur sand are constantly dissolved and swept along by the currents; (b) 
the innumerable hot and cold springs and geysers along the shores, which con- 
tain sulphur, and sometimes arsenic and other compounds. Some of the springs 
may rise from the river bed ; hence they are submerged for a good part of the 
year and become exposed only during the low water stage of summer. The 
spring seen in figure 79 is of this type, and was exposed only when the water 
had dropped about twenty inches. 

Practically all other streams in the Park carry considerable amounts of 
sulphur in suspension during the flood period and their waters are not very 
palatable and refreshing during that time. But as the waters grow clear, 
that is, as the sulphur sands have silted out, they improve in potability. More- 
over, the fish then lose the sulphury taste they all seem to have during the 
flood period. 

Turbidity. Due to the materials in suspension, most mountain streams are 
very turbid during the flood periods. Usually by the middle of July the waters 
become clear. Temporary turbidity, however, is quite frequent, and is caused 
by rains and by shore slides. Unless the rains have been very severe, the 
temporary turbidity lasts only a few hours. Where a mountain stream passes 
through large upland meadows, as is the case with the Gardiner River and 
Slough Creek in Yellowstone Park, the Clearwater, Oro Grande, Wietas, and 
Forks of the Elk River in Idaho, and the Flathead and St. Mary’s rivers in 
Glacier Park, — the rains wash down considerable quantities of mud, and this 
requires a much longer time to sediment out than do the sulphur sands. 

As a matter of fact, local turbidity occurs quite often, due to the dislodg- 
ing of some rock by the current or some passing animal. This temporary and local 
turbidity seems to have the effect of making the moving fauna scurry into shelters. 

Aeration. The continuous and marked descent of waters in mountain 
streams results in a thorough churning and mixing of water with air, and hence 
in a high oxygen content. Oxygenation reaches its highest level in mountain 
waters since, besides the churning, the low temperature permits the absorption 
of greater quantities of oxygen. 

Temperature. A characteristic of a mountain stream is the uniformity of 
its temperature. The constant churning and mixing does not permit a thermal 
stratification such as one finds in quiet streams, lakes, ponds and swamps. 


Roosevelt Wild Life Annals 


176 

Temperatures taken in Yellowstone River at the bottom of deep “holes,” in- 
eddies and in rapids, were all identical. There is a difference among streams, 
however. Small creeks such as Lost Creek rose rapidly in temperature ; here 
the heat reflected from the slopes raised the temperature of the water as much 
as 8° C. 

An interesting fact is that the waters of Yellowstone Lake, before passing 
into the outlet, absorb considerable heat from the sun. As a result, the river 
in later summer showed a higher temperature than the Lamar River, or Tower 
Creek. Streams that are fed by many springs do not freeze over in winter. 

Circulation In lakes, ponds and slow streams circulation is affected' 
chiefly by winds and convection currents. As a result a thermal stratification 
is established and with it a stratification of dissolved gases. In mountain streams 
circulation is direct and complete. The constant descent of water results in a 
thorough mixing, so that both temperature and oxygen content are equalized 
throughout all parts of the stream. This is one of the most marked physiological 
differences between mountain streams and other aquatic bodies. 

In summary, current caused by the descent of water is the primary extrinsic 
factor, which in turn affects the aeration, temperature, circulation and 
transparency of the stream. 

Intrinsic Factors. Except for certain Tipulidae larvae burrowing along the 
shores among rocks, the primary fauna of trout streams is confined to water 
breathers, i. e., such as obtain their oxygen from the water. The speed of the 
current precludes any sort of emergent vegetation, which latter is essential for 
surface breathers, i. e., breathers of atmospheric air (see Muttkowski, ’21). 
Among animals, therefore, only such as breathe oxygen in solution in the water 
are found — in general, only such types, especially among insects, as require a 
high degree of oxygenation. 

Because of the currents, the biota is further limited to species that are 
either strong swimmers or strong dingers — the latter directly by means of struc- 
tural adaptations (claws, suckers) or indirectly by means of clinging devices 
constructed by the various species (webs, jellies, attached cases). 

The current causes a third limitation, namely, in the matter of food supply. 
Species living here cannot limit themselves to plant or animal food, or as in 
quiet habitats, to some one particular type of plant or animal. On the contrary, 
favorable locations here are more isolated — “biotic islands,” one may say, where 
a few plants and animals assemble ; and a hungry specimen must eat whatever is 
available. Indeed, one finds that habitually carnivorous and herbivorous species 
both become mixed feeders in mountain streams. On the whole, the highly special- 
ized conditions call for specialization in structure, but for generalization in diet. 

In summary, the current and resultant high oxygenation are the dominant 
intrinsic factors which affect the physiology of a stream. These at once limit 
the biota (a) to water breathers, (b) to active swimmers and dingers among 
water breathers, and (c) to indiscriminate feeders, i. e., species of unrestricted 
diet. 

A further restriction arises from certain special habits. As noted in a 
previous paper (Muttkowski, T8, p. 386), a special habit may eliminate a species 


177 



Fig. 7 1. Rocks at eddy of Lamar River. Low water stage. In June these were 
completely covered by the floods. Sept. 4, 1921. 



Fig. 72. Stream bed of Lamar with recession pools. Aug. 8, 1921. 




178 



Fig. 74. Lost Creek Falls. Sept. 2, 1921. 






Ecology of Trout Streams 


179 


from a habitat which it might otherwise inhabit. This was instanced by 
Odonata. many of which deposit their eggs on or in emergent vegetation. 
Where such plants are absent, these Odonata will not be found, although they 
are water breathers. 

QUALITATIVE LIST OF PLANTS AND ANIMALS 

The following lists cover only the more dominant or “type forms” of moun- 
tain waters. Xo attempt was made to secure a complete collection of the species : 
only enough to ascertain the dominant types, to learn something of their rela- 
tions to the environment, and of their interrelations with one another. Further, 
only the native biota is considered. Attention has already been directed to the 
ecological distinction between primary and secondary inhabitants, or between 
native and invading species. Such plants, for instance, as Elodea, Nymphaea, 
Castalia, Potamogeton, may occur at some rare point in a mountain stream, where 
for some reason or other the current is greatly diminished and permits a slight 
amount of plant growth. But such single occurrences hardly warrant their 
being listed as native species. 

A further restriction must be noted because of the taxonomic difficulty. 
This arises from the fact that in so many species one deals with immature stages, 
many of which are as yet unknown to taxonomists. This fact was realized long 
before these studies were begun. In the Park a distinct and prolonged effort 
was therefore made to secure complete “life histories” of many insects. In 
fact, I tried to breed many stages. Cans and jars, partly filled with stones and 
covered with cheese-cloth, mosquito bar or wire screening, were placed at advan- 
tageous points in Lost Creek, where human intruders were rare. Alas ! While 
my security from humans proved complete, I had not anticipated the insatiable 
curiosity and impish destructiveness of the bears. Day after day, despite my 
best efforts in hiding my experimental jars, the bears searched them out 
and despoiled or destroyed the jars and their contents. This lasted for more 
than four weeks, after which I surrendered to the superior patience of the bears. 

This is not offered as an excuse, but to signify a real condition that con- 
fronts the investigator at times in Yellowstone Park. Visitors in the public 
camps frequently use the streams to refrigerate some of their food supplies 
during the night. This the bears seem to know and very often seek out the 
“caches” for a toothsome morsel. Some of the bears are known to plunder the 
food boxes which campers carry in their cars or on the running-boards. Being 
possessed of curiosity, the bears would quite naturally seek to know what was 
hidden in the jars I had planted in the stream bed. The results were dis- 
astrous so far as my breeding experiments were concerned. 

In view of this, I tried so far as possible to secure representatives of various 
stages of insects, to be associated later on if possible. Such a method is unsatis- 
factory, of course. But under the circumstances it offered the nearest approach 
toward securing complete life histories. 

The Plants. The list of plant species given below is copied from 
Muttkowski and Smith’s, The Food of Trout Stream Insects in Yellowstone 


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Roosevelt Wild Life Annals 


Park (Roosevelt Wild Life Annals, Vol. 2, No. 2). This list was based on 
certain surveys made for the purpose of checking the food available in given 
localities with that actually eaten by insects found in the same places. 

A marked characteristic of mountain streams is the total absence of higher 
plants. Lower plants, too, when present at all, are none too conspicuous and 
generally are confined to one or two forms of algae. When these occur, they 
are present for only short periods. Thus, Cladophora was found in the Lamar 
River in considerable quantities for about four weeks; the entire bed of the 
stream was decorated with bright plumes, so that from a distance the water 
appeared a bright green. But in about four weeks most of this luxuriant growth 
was gone and the remainder was a sparser and shorter growth of Cladophora. 

The same held true for the Gardiner River. In Yellowstone River 
Cladophora was very scarce, an occasional plume occurring in some sheltered or 
less exposed spot. In Tower and Lost creeks, also, for some unexplained 
reason (perhaps due to lack of carbonates), Cladophora was scarce. On the 
other hand, in Lost Creek, Tower Creek, Lava, Blacktail Deer, Hellroaring, 
and other creeks, the flat Prasiola was fairly abundant and associated with a 
type of Nostoc. This same scarcity of Cladophora was noted in 1925 in the 
streams and lakes of Glacier Park. 

Besides Cladophora. smaller filamentous algae and various diatoms thrive 
among the small accumulations between rocks ; this includes such forms as 
Melosira, Ulothrix, Closterium, Cocconeis, etc. In the marginal pools Spirogyra 
may thrive temporarily. 

Following is the alphabetical list : 


Cladophora sp. 
Closterium sp. 
Cocconeis sp. 
Epithemia sp. 
Gomphonema sp. 
Melosira sp. 

Moss — undetermined. 


Nostoc sp. 
Oscillatoria sp. 
Prasiola sp. 
Rhoicosphenia sp. 
Spirogyra sp. 
Synedra sp. 


An occasional battered fragment of Potamogeton, Chara, or other lake plant 
might also he found in Yellowstone River, washed down from the lake. 

The Animals. The specialized conditions of mountain streams restrict the 
number of animal species very markedly. In Yellowstone Park only three of 
the Phyla can be called endemic, namely the Platyhelminthes, Arthropoda. and 
Chordata. For Idaho, Washington, and Montana, certain additional phyla can 
be noted — at least for some of the streams. Besides these representatives of 
other phyla are of sporadic occurrence. 

a. Invertebrate Phyla (exclusive of Arthropoda) . 1. Protozoa. — Only the 
Yorticellidae and the parasitic Gregarina can be considered as native in the quick- 
flowing mountain streams. One finds them more frequently, however, in the 
marginal and sheltered pools left by receding flood waters. Where the current 
is strong: thev do not occur, as a rule. Occasionallv, where small masses of 
filamentous algae, e. g., Cladophora. Melosira, Oscillatoria, etc., have become 


i8i 



Fig. 75. Lost Creek, low water stage. In June all the stones 
were covered by water. Sept. 2, 1921. 



Fig. 76. Lost Creek, low water stage. Showing the last pool in 
the bed of the stream. The stream is dry for nearly a 
hundred yards above this point. Sept. 2, 1921. 





Fig. 77. Tower Creek, confluence with Carnelian Creek (right). Sept. 6, 1921. 



Fig. 78. Tower Creek in Tower Creek Canyon, showing the thickets along banks and 
stones in bed of stream. Aug. 14, 1921. 





Ecology of Trout Streams 


183 


wedged between rocks, or have formed accumulations at stagnant points, various 
Protozoa do occur, such as the ubiquitous V orticella, Paramecium, several species 
of Ameba, Oxytricha, Colpoda, etc. 

A second condition under which one may find the Protozoa in rapid waters 
is within the shelters formed by other animals, such as the cases of Trichoptera 
and the tubes of Chironomidae. Here they may lodge, or attach themselves to 
the occupant, a habit that applies particularly to the Yorticellidae. Empty 
cases and tubes often contain a surprisingly varied microscopic life. 

Among the deposits on stones, particularly those of the “holes,” the \ orti- 
cellidae frequently form colonies of considerable size, numbering many 
thousands of individuals. 

Perhaps most surprising is the wide occurrence of Grcgarina in the various 
aquatic insects, especially in Trichoptera. As noted in a second paper (see 
Muttkowski-Smith), the specialized conditions of the habitat force a general- 
ization in diet. It seems that insects and other animals are readily crushed, 
and such fragments are avidly eaten by nearly all the different insects inhabit- 
ing the mountain streams. Frequent catches made with plankton nets demon- 
strate this fragmentation clearly. It is by eating these fragments that insects 
spread the Gregarina among themselves ; for certainly the Grcgarina are entirely 
passive in this matter. 

2. Porifera, Coelenterata. Neither sponges nor hydrozoans are found in 
the rapid w'aters, although they are of frequent occurrence in adjacent ponds 
and small lakes. In European mountain streams several species of Hydra have 
been noted in very placid stretches of their waters. These species can hardly 
be considered as native. 

3. Rotifera. Rotifers are of sporadic occurrence, being usually found 
together with Protozoa in mats or wads of filamentous algae. Their occurrence 
seems chiefly accidental. Insects feeding on the algal mats will readily devour 
the rotifers and other small animal life. In the larger streams of the North- 
west, such as the Snake. Clearwater, or St. Joe, one may find Rotifera in quiet 
stretches, especially where the streams pass through great meadows. 

4. Platyhelminthes. Two species of flatworms are very typical of the 
western mountain streams, namely, Polycclis nigra Ehr., and Dendrocoelium 
lacteum Mueller. The black Polycclis is very common, the white Dendrocoelium 
much less frequent. The larger the stream, the less the abundance of these 
flatworms. The optimal habitat seems to be that of moderate sized streams. 
In Tower Creek most of the stones had numerous specimens on their under 
sides, where the worms moved rapidly on their slime trails, feeding on the 
various rock diatoms growing there and on the shore diatoms swept along by 
the current and caught in the slime films. They reach a length of about 18 mm. 

The scarcity of flatworms in Yellowstone River may possibly be due to 
the great amount of sulphur carried by the stream. Still, Tower Creek and 
Lost Creek both carry large quantities of sulphur, at least during the flood 
period. On the other hand, the small number might be explained on the basis 
of too strong a current. But here again it must be noted that comparatively 
speaking the current in Tower Creek is faster than that of the Gardiner and 


184 


Roosevelt Wild Life Annals 


Lamar rivers; yet Tower Creek is an ideal stream for flatworms and they occur 
there in multitudes. In fact, in Lava Creek, which is still more rapid, the 
flatworms are even more abundant. 

5. Nemathelminthes. Except for a parasitic Mermis sp. found in 
Simulium larvae and mayfly nymphs (Fig. 103), and an occasional Gordius 
larva, the round worms and hair worms are absent. Thienemann finds that 
Mermis and Gordius in their last or adult stages like to burrow in the wet soil 
at the margins of spring-fed pools and also among the deposits on rocks. 

6. Mollusca. To my surprise I did not find any snails or clams repre- 
sented in any of the mountain waters. This is contrary to the findings of 
Steinmann for Switzerland and of Thienemann for Germany. Xot even the 
univalve Ancylus was noted. Only in quiet stretches where the streams flow 
through the higher meadows, do occasional Planorbis and other snails occur. 

7. Annulata. Annulate worms and leeches seem to be entirely absent from 
the streams examined in Yellowstone Park. Only one specimen of a Pristina 
was found on August 31 in Yellowstone River. Very probably this came from 
an egg that had floated down from Yellowstone Lake. In this respect the larger 
streams of Idaho show some difference. Thus in the Clearwater and Snake 
rivers an annulate, probably a Limnodrilus , is quite abundant in the clear rapids. 
Leeches, too, occur in the Clearwater, under the shore rocks. These shores 
recall the lake shores markedly, since similar species occur in both, e. g., leeches, 
flat mayfly nymphs ( Hcptagenia sp., etc.), Pscphcnus (Fig. 1 1 5 ) , flat 
Trichoptera cases, hydroptilids, etc. 

b. Arthropoda. The Arthropoda contain the dominant forms of the moun- 
tain streams which could be studied more carefully in their interrelations. 

1. Crustacea. Crustacea are conspicuous by their absence from the moun- 
tain streams of the Parks, Yellowstone and Glacier. Yet in the large trout 
streams of Idaho and Washington, such as the Clearwater, St. Joe, Spokane, 
the St. Mary’s in Montana, etc., one finds Cambarus quite frequently, and 
occasionally Hyalclla and some forms of Gammarus. Smaller plankton 
Crustacea, too, may occur. This distribution in Idaho may be due to the 
greater amount of mud present in the streams, and the many long placid 
stretches where the streams move through the “upland meadows.” Perhaps 
the lower altitude (3000 ft. and less in the places examined), may have some- 
thing to do with the Crustacean representation. Thienemann calls attention to 
the fact that the chemical composition of the waters, particularly the carbonates, 
affects the faunal composition in very marked manner. It is possible that the 
paucity of Crustacea and Mollusca in the Park streams is to be associated with 
the presence or absence of the carbonates. Unfortunately. I had neither the 
time nor the requisite equipment to determine this. 

From the parasitic viewpoint also the Crustacea do not seem to be estab- 
lished in the Park. Of the several hundred trout examined only one was 
found to have a copepod gill parasite. 

2. Arachnida. Shore and rock spiders were observed quite commonly in 
their hunts along the stream. Their main prey seemed to be the adult caddis- 
flies. On overhanging rocks, on the bridges, and on trees along the shores. 


Ecology of Trout Streams 


185 


webs of other species were found which contained caddisflies, mayflies, and 
smaller stoneflies (Figs. 97 and 98). Such webs are often nothing more than 
irregular tangles of silk, anchored here and there, hut not stretched out in 
any regular fashion. The spiders seem to he able to run on the surface film 
of the water for short distances. Thus, on September 1 a number of spiders 
were observed on Tower Creek, running close to the water, or even skating out 
on the surface film after caddisflies. 

These spiders no doubt account for a considerable number of adult aquatic 
insects. The caddisflies formed by far the major portion of the web contents. 
In turn the spiders occasionally fall prey to the current and are eaten by the 
fish. 

Hydrachnida, like the Protozoa, Rotifera, Mollusca, and Crustacea, are not 
native in the mountain streams of Yellowstone Park. In the smaller streams 
they are sporadic, usually where a slight tendency to swampy conditions mani- 
fests itself. In Lost Creek I found Hydrachnida in beaver ponds. In the 
Lamar they occurred in empty Trichoptera cases and among the mosses in 
very shallow water. Both Steinmann and Thienemann record a number of 
species for the streams of Europe. 

3. Insecta. Perloidea. — The stoneflies form the dominant invertebrate 
animals of the mountain streams. While they also occur in other aquatic bodies, 
such as lakes, ponds, and slow streams, their optimal habitat is rapid waters, 
particularly the cold mountain streams, with rapids, cascades and falls and 
therefore with a high degree of oxygenation — precisely the type of waters pre- 
ferred by trout. One may say that trout and stoneflies are intimately 
associated ; where one occurs, the other also is found. 

In Yellowstone Park about a dozen species were captured ; and of these 
about five were numerous and conspicuous, the remainder occurred more spar- 
ingly. In habitus the larvae are very dissimilar, a fact which correlates with 
their habits and habitats. Thus the largest species. Pterqnarcys calif ornica (Fig. 
99), is conical and long, the sulphurous Acroneufia pacifica short and squat, 
with Acroneuria tlieodora intermediate in shape, somewhat short, but less 
markedly flattened. This divergence in shape is associated with divergence in 
habits. A. pacifica is primarily a clinging species ; it hunts the undersides of 
rocks in strong rapids. Ptcronarcys calif ornica is a roving type, and hunts 
between rocks; it migrates freely from pools to rapids, and from midstream 
to the shores in search of food. The various species of Allopcrla are elongate, 
only slightly flattened, and are found at the bottom of pools or “holes” where 
the surface current sweeps above them and leaves the bottoms relatively 
undisturbed. They, too, are rovers. 

Following are the species determined; Ptcronarcys calif ornica Newport. 
Pteronarcclla badia Hagen, Pcrlodcs Hagen, Acroneuria pacifica Banks, 
Acroneuria ( Donoroncuria ) tlieodora Needham and Claassen, Pcrla verticalis 
Banks, Isoperla j-punctata Banks?, Allopcrla coloradcnsis Banks, A. lineosa 
Banks, A. fidelis Banks, A. sp. 

Of these Pteronarcys californica is most conspicuous, by virtue of its size 
and bright salmon color, although it is really less numerous than its sulphur- 


Roosevelt Wild Life Annals 


1 86 

colored relative, Acroneuria pacifica. This, the largest of stonefly species, has 
received a number of popular or local names, according to color, region, shore 
vegetation, and the kind of fish found; thus one meets with names such as 
salmon flies, trout flies, mountain flies, red flies, river flies, willow flies, grass 
flies, etc. 

The larvae attain a size of three to three and one-half inches fFig. 9 9). 
In color they are a dull blackish gray, with yellow or orange dorsal and lateral 
stripes. Their form is conical, widest at the thorax and narrowest at the caudal 
end. They are good swimmers, but move mainly by creeping among the rocks 
in the weaker rapids, eddies, and bottoms of pools. Strange to say they eat 
plant food almost entirely, dififering in this respect from other perloid nymphs. 
Thus, the stomach contents of both young and full grown nymphs were diatoms, 
bits of algae, wood, and bark, while those of other stonefly nymphs were chiefly 
animal matter. The roving habits of this species make it a favorable food item 
for trout, more so than any other perlid species. 

Transformation appears to coincide with the recession of the spring floods, 
when the waters are still turbid and a Secchi’s disk is visible for scarcely ten 
inches. In 1921 transformation began on July 5 at the Cooke City Road bridge 
(Fig. 70) over the Yellowstone, and lasted for about a week, although some 
belated stragglers continued to emerge till July 26. But the peak of transforma- 
tion was July 5 to 8. Curious to say, the transformation at this point did not 
coincide with the upstream and downstream emergence. Upstream, in the stretch 
of river between the lake and Upper Falls and in Yellowstone Lake final eedysis 
was pronounced from June 25 to 30, according to reliable information received 
from Mr. Ainesworth, of the Lake fish hatchery. Downstream, at the eddy at 
the mouth of Elk Creek, this species transformed in large numbers on July 15 and 
16. Opposite Hellroaring Creek transformation was very pronounced on July 
19 for both this species and Acroneuria pacifica. Visitors at Camp Roosevelt 
from points north of the Park reported that large numbers were emerging on 
Inly 21, along the Gardiner-Livingston highway which parallels Yellowstone 
River. 

Interpreting these dates in a linear arrangement, it would seem that trans- 
formation proceeds in a wave downstream, being earliest at Yellowstone Lake 
and progressively later at points farther down. In how far these dates accord 
with those of other years is problematical. According to Mr. A. G. Whitney, 
in 1922 recession of water occurred earlier and the stoneflies appeared about 
two weeks earlier than in the preceding year. 

Transformation takes place early in the day, within the first four hours 
after sunrise, the greatest number emerging at about eight o'clock. Stragglers 
continue to emerge practically all morning — indeed, occasional specimens were 
observed transforming in the afternoon. For eedysis the nymphs climb up 
any convenient point along the shore — into grass, onto stones, brush, trees, etc. 
(Figs. 100 and 102). On the whole, they prefer open places along the stream. 
Also, the slack waters of eddies are sought. In rapids, the various emergent 
rocks, and in smooth stretches some mid-stream boulder, form convenient places 
for emergence. Eedysis then takes place on the shaded side of any object to 
which the nymph has anchored itself by means of its legs. 


18- 




Fig. 80. Cleft boulder on meadow between Yellowstone and Lamar rivers. 

June 17, 1921. 


1 88 



Fig. 81. Brink of Lost Creek Canyon to right, and “crater” in foreground. The 
meadows are said to be the bottom of the crater, the hills around forming the 
rim of an extinct volcano. Aug. 28. 1921. 



Fig. 82. Castle Rock (also called Cathedral Rock) on North Fork of Clearwater 
River, Idaho. Showing types of shores and placid stretches of stream. Sept. 
2, 1924. 





Ecology of Trout Streams 


189 


The slow pumping action and inflation to split the nymphal skin can be 
readily observed. Eventually the skin splits on the dorsal side on a line between 
the wing pads and the occiput, the thorax pushes up and through the slit, the 
feet are partly withdrawn, then the head, the entire thorax and legs, and finally 
the abdomen. The whole process may take from twenty minutes to an hour. 

Spreading of the wings then proceeds, during which process the adults 
generally cling to their exuviae. The adults take flight in a very few minutes, 
while the wings are still very soft and pliable. They fly to some higher object 
near the stream, generally to some tall bush or small tree ; and if a person be 
in the vicinity, he too may serve as an alighting place and shortly may be 
covered with these fluttering insects. Observation indicates that the points 
sought are such as give suitable exposure to the light and to the breezes for 
the purpose of drying their wings ; direct sunlight is never sought. The adults 
spread and move their wings freely during this process. In addition, they exude 
yellow or salmon-colored droplets from the anus, which may be blood or merely 
waste products, it is unknown which. 

Copulation in this species takes place late in the day, oviposition appar- 
ently at any time in the day. For oviposition the female descends on rocks to 
the water surface and dips her abdomen into the water and permits the eggs 
to be washed off in the lesser currents along the shore. 

A curious phenomenon noted for this species and for Acroneuria pacifica is 
the crepuscular flight upstream. This begins immediately after sundown and 
lasts till after dark. Swarms of thousands of specimens take flight, hovering 
from 50 to 200 feet above the water, depending somewhat on the height of the 
shores. Since both sexes participate in this flight, it might be regarded as a 
“nuptial flight.” But, as already noted, copulation does not take place during 
flight, but when the specimens alight in tall grass, low trees, and bushes, or 
lacking these, in crevices of rocks, or grooves in the sand. It is therefore not 
at all clear how this flight is to be interpreted. Practically, however, the. instinct 
serves effectively to repopulate the headwaters of the various streams. During 
the upstream flights numberless thousands are caught in the vortices, back 

drafts, and wayward air currents, and are hurled to the stream beneath, where 

they eventually form an important item of the surface food of trout. 

Adult life normally lasts but three to four days. Relatively few specimens 
die a natural death. Being awkward fliers, during their short flights they are 
readily swept into the water by wayward air currents. Others form juicy tid- 
bits for hundreds of birds. Still others may be eaten by small mammals. In 

the morning one finds hundreds of severed wings along the shores of the 

stream, indicating perhaps the active feeding of the birds during the early 
hours. One morning, at a point near the Cooke City bridge, in a gravelly 
depression about three feet in diameter, I counted the wings of over 200 P. cali- 
fornica and A. pacifica. Most of these I removed. Next morning an approxi- 
mately equal number of detached wings lay in the same depression. I was 
unable to tell whether mammal or bird or other creature had feasted there. 

Ptcronarcys calif ornica is primarily a river species, abundant only in the 
larger mountain streams, and rather scarce in the precipitous creeks. It is 
found throughout the Northwest. 


Roosevelt Wild Life Annals 


190 


Acroneuria pacifica, which is very closely associated with P. calif ornica, was 
even more abundant. In the main, what has been said about the larger species 
applies also to A. pacifica, with the exception that the nymphs are quite squat 
and smaller, and that they are much more active. On shore the adults also 
seem to be more active than the larger species (Figs. 101 and 102). 

For July 21 I have the following note: “Yellowstone River shores strewn 
with wings of P. calif ornica and A. pacifica. Many caught in spider webs 
with Tipulids and caddisflies. Many others water-trapped. Eaten by birds (night- 
hawk, robin, etc.). Also snakes (garter snake) here that feed on the adults. 
Ground squirrels seen twice feeding on Pteronarcys adults.” 

Garter snakes were seen on various occasions feeding on stoneflies. Julv 
15 six garter snakes were observed feeding on these insects in the stone rubble 
that marks the Elk Creek eddy of the Yellowstone. On July 16 some twenty 
garter snakes were noted along the Lamar, most of them feeding on the stone- 
flies. A frog taken along the I^amar and examined for the stomach contents 
showed several adult Acroneuria, a beetle, and some diptera. 

Of other species, Acroneuria thcodora deserves mention. Its emergence 
occurred early in August along the Gardiner and Lamar rivers. Very few 
adults were seen and none of the nymphs, except for some exuviae. This is not 
a common species. 

The smaller species of stoneflies, with adults of pale greenish or yellowish 
hue, are somewhat inconspicuous because of their small size. One finds the 
nymphs most frequently among the rocks on the bottom of midstream pools, 
and very sparingly among the rocks of rapids. Their food is chiefly animal 
matter. Their emergence seems more prolonged, and not confined to a rela- 
tively short period like that of the larger species. On the whole, the smaller 
species are much more abundant in smaller creeks and along the shores of 
mountain lakes than in the larger streams. 

Insecta. Epherneroidca. — Of the mayflies the following have been identi- 
fied: Am el etas sp., Callibaetis sp., Drunella grandis, Ephemerella eoloradensis, 
Ephemerella sp., Hcptagenia sp., Iron longimanus. This list is rather frag- 
mentary, since most of the species were available only in nymphal form. An 
attempt to breed the nymphs has already been mentioned ; to the persistence of 
the hears in wrecking my arrangements may be ascribed the lack of more specific 
identifications. 

Two types of habitus are present among the nymphs, the swimming and the 
clinging. Thus, one encounters the cylindrical and slender nymphs as typified 
by Bactis and Callibaetis, and the flat appressed type of Hcptagenia, Iron and 
other forms. 

The food, as indicated by examination of the stomach contents, is largely 
offal. The food average for 25 Ameletus nymphs was: plant food 2 2.~ c c, 
detritus 77.3% ; for twenty Drimclla, 18.6% animal food, 36.8% plant food, and 
44.7% detritus ; for two Bactis, 50% plant, and 50% animal food ; for 28 
Ephemerella, 3.6% animal, 36.3% plant food, and 60% detritus; and for 34 
Hcptagenia, 24% plant food and 76% detritus. 


Ecology of Trout Streams 


HJl 


Some of the Drunella nymphs were heavily infested with Gregarina. On the 
other hand, two Heptagcnia nymphs were found to be parasitized by a nema- 
tode parasite ( Mcrmis sp.). Figure 103 shows an adult mayfly with such a 
parasite emerging. The specimen was taken at the entry of Lava Creek into 
Gardiner River ; it was fluttering weakly and the weight of the parasite held 
it from rising above the shallow rapids at that point. 

Transformation for all species was very irregular and seemingly strung 
out during the whole summer. One could expect to find a few adults trans- 
forming every day. No attempt was made to secure a series of adults. This 
was mainly for a personal or selfish reason. Usually laden with bottles, water 
nets, cameras, luncheon, etc., an extra net and cyanide bottles might be more 
of a load than would be comfortable for a tramp of many miles. 

Insecta. Odonata.- — Relatively few dragonfly species are known from 

rapid streams, and even fewer from mountain streams. Only a single species, an 
Ophiogomphus (probably montanus Selys), was found, of which three adult 
females and some eight or ten exuviae were collected. Strange to say, all of 
these were found in one locality, some fifty yards below the Cooke City bridge 
across the Yellowstone. On July 30 the emergence of a specimen was observed 
in detail. The following is taken from my field notes of that date: 

“10:37 a - m. — Gomphid climbed out of water. Immediate shore here is 
somewhat sandy. Climbed onto rock. 

10:45 — Thorax split open. 

10:46.5 — Head and thorax thrust forth. 

10:50 — Head, thorax, and legs out. 

10:58 — Abdomen out to 4th segment, wings elongating. 

1 1 : 02 — Abdomen out completely. 

11:05 — Wings unfolded to one-half their adult length. Abdomen shows no 
change. 

11:12 — Wings open to stigma. 

11 :I4 — Wings open to tip, now y?, longer than abdomen. 

11 :i5 — Abdomen beginning to be inflated, insect clawing for hold on rocks 
and exuviae. 

11:17 — Insect leaves skin for hold on rock. 

11:18 — Pumps abdomen with visible effort, swaying from one side to other. 

11:20 — Abdomen extends to beginning of stigma on wings. The wings 
are folded roof fashion to side of abdomen, which is pressed firmly against them, 
to aid in process of inflation. 

11:21 — Abdomen extends to end of stigma. 

11:21.5 — Droplet forms at end of abdomen and drops into water. 

11 :22 — A second droplet. 

1 1 :22_3 — Third droplet. 

11 :22.4 — Fourth droplet. 

11:22.5 — -Fifth droplet. 

11:22.8 — Sixth and seventh droplets. 

11:23 — Eighth droplet. 


192 


Roosevelt Wild Life Annals 


11:23.5 — Ninth droplet. Abdomen reaches to tip of hind wings. 

11:24 — Three droplets in rapid succession. 

11 :25.2 — Two more droplets. No more fell after this. 

11 :28 — Abdomen extends slightly beyond tips of hind wings. 

11:30 — Abdomen V) in. beyond tip of wing. 

11:45 — Abdomen deflated. 

11:50 — Leaves for top of rock and extends wings for flight. Captured 
on ‘take off.’ ” 

Two other females were captured the same day. Specimens of this species 
were also seen on the following days along the Gardiner and Lamar rivers, 
but were not captured. 

In the neighborhood of mountain streams one frequently sees specimens 
of Sympetrum, Aeschna, Lestes, Enallagma and other pond forms. These 
come from nearby quiet waters, or. as in the case of Lost Creek, may even 
occur in beaver ponds; that is, in such ponds as result from damming of the 
flow of the creek by the beavers. The fauna of these ponds is of a mosaic 
type, as a rule, consisting of a very few representatives of pond life. 

Insecta. Hemiptera. — The aquatic bugs are hardly endemic to moun- 
tain streams. Like many other aquatic insects, they may occasionally be found 
in marginal pools, ponds, and in swamps and springs. Thus. Notonccta may 
be found on rare occasions and with it Corixa, and more frequently some water 
strider or surface skimmer. In Yellowstone Park I encountered water striders 
on the Lamar, Tower Creek, Lost Creek, and Gardiner River; invariably they 
marked the neighborhood of some spring-fed pool or clear pond. In Idaho I 
have seen the skimmers along the Snake. St. Joe. Clearwater. Elk. and Oro 
Grande rivers, in Glacier Park along MacDonald Creek. Two Medicine River, 
St. Mary’s River, etc. There, too. they seemed to he migrating from some 
neighboring pools. 

Ixsecta. Trichoptera. — Only generic identification was possible for most 
of the species taken, due to lack of adult stages. For here. too. the bears 
interfered. For breeding cages I had used some of the familiar cone-like fly 
traps of wire, which were fitted over stones harboring various caddisworms. 
These the bears were not satisfied to tip over, but removed them completely ; 
I did not discover what they did with the traps. Following are the species 
determined : Brachyccntnis sp., Glossosoma sp., Gocra sp., Hydropsychc scalaris 
Hagen, H yd ro psyche sp.. Limnophilus sp. (near rhombicus L.), Molanna sp.. 
Ncopliylax concinnas Hagen. Philo potamus sp.. Platyphylax sp.. Rhyacopliila 
eoloradensis Banks, R. fnscula Hagen, R. tori'a Hagen, R. sp., Thrcnuna sp., 
Triacnodcs sp. 

Of these species the four most conspicuous are Hydropsyche, R. torva, 
Brachycentrus sp. and Thrcmnia sp. Of these the first is a web-spinner, the 
following two have fixed cases, and the last a movable case (except during the 
pupal stage, when the case is fastened). In the creeks Thrcnuna and Hydro- 
psyche seemed abundant, in Yellowstone River the other two species. 
Hydropsyche, strictly speaking, is of wider distribution than other species of 
the mountain waters. 


193 



Fig. 83. Clearwater River, Idaho. Showing sand deposits left by spring flood, 
and log jam in river. Aug. 31, 1924. 



Fig. 84. Clearwater River, Idaho. A closer view of log jam caused by spring 
flood. Also showing “The Gates” and government bridge across river. Aug. 
3 b 1924- 



194 



Fig. 85. Hibernating Coccinellidae. Photograph taken on a warm spring day when 
sun brought out the beetles. Many had been w'ashed into a creek about twenty 
feet away. Photograph Moscow' Mt., Idaho, about April 15, 1923. 



Fig. 86. Skeleton of winter-killed buffalo, near Lamar River eddy. Note the 
puparia of flies on the scapula. The skull had been dragged into the eddy by 
some animal (bear?). July 25, 1921. 




Ecology of Trout Streams 


195 


The fixity of the cases results in an enormous death rate for Brachycentrus 
and Rhyacophila. During the high water period their cases are attached to 
rocks that are then submerged; with the quick recession of waters these cases 
are “stranded” and their inhabitants die within them (Fig. 104). On several 
occasions a number of these stranded cases were opened to see if the larvae 
had left them in order to build new habitations. The stranded cases contained 
dead larvae and pupae. Very quickly these form the food for scavenging shore 
forms, such as Staphylinidae, a Silpha, Carabidae, and ants of various kinds. 
This “death by stranding” was most notable along the Lamar River, where 
the recession of water was very rapid. 

For Brachycentrus two methods of attaching the square cases were noted. 
One was to attach them by the base, i. e., the small end, so that the cases stuck out 
from the rocks at right angles (Figs. 104 and 105). The second was an 
attachment by means of a “lip” at the wide or head end of the case ; usually 
this occurred close to the surface so that the surface layer of water , would 
sweep directly into the case. When a stone carrying such cases was lifted 
above the water surface or to a point where the water did not completely cover 
the opening, the larvae would pull the case to an oblique or right angle to the 
rock, bite off the secretion attaching the case and then crawl down the rock 
to a point where the current was suitable. The cases were submerged from 
one-fourth of an inch to six inches in fairly strong rapids. 

Empty cases of Brachycentrus seem to afford opportunity for the develop- 
ment of a micro-fauna of their own, particularly of Protozoa, Rotifera, and 
an occasional Flydrachnid. 

The food of caddisworms is quite generalized. Thus, 32 Rhyacophila con- 
tained 49% animal food, 23% plant food, and 28% detritus; 27 Hydropsyche 
had eaten 42% animal food, 54.3% plant food, and 3 .7% detritus; 33 Brachy- 
centrus consumed 18.3% animal food, 72.7% plant food, and 9% detritus; 
and 23 Thremma included 28% animal food, 64% plant food, and 36% detritus 
in their diet. On the whole, the first three take their food as it comes to them, 
while Thremma selects what food it consumes. All of the forms are cannibals 
on occasion (see Muttkowski-Smith) . 

Connected with the feeding one may note the extent to which the various 
species are parasitized — Rhyacophila with Gregarina in about 40% of the 
specimens examined, Hydropsyche about 60%, and Brachycentrus fully 100%. 
None of the specimens of Thremma contained any parasites. This is possibly 
correlated with the fact that their food was primarily selected, while the other 
forms ate what food was swept along with the flotsam down the stream. Much of 
this flotsam consists of crushed and torn specimens of insects. 

The adults have the habit of flying above rapids, running up the wet rocks, 
and also dipping into the water. This habit exposes them to capture by fish ; 
indeed, they were numerous among the stomach contents of trout. One trout 
was found to have gorged itself with caddisflies, the total number exceeding 
500 specimens. 

Insecta. Diptcra. — Only three families can be said to be typical in moun- 
tain streams. These are the Blepharoceridae and Deuterophlebiidae, or net- 


196 


Roosevelt Wild Life Annals 


winged midges, and the Simuliidae or Buffalo gnats. Besides these, isolated 
genera of Chironomidae, Leptidae, Tipulidae, and Psychodidae breed in rapid 
streams. In addition, the adults of some species must be listed as hovering near 
swift water, chiefly on rocks that are sprayed by the stream. 

The most typical residents of swift streams are the Blepharoceridae. This 
family was represented by two species, Bibiocephala comstocki and B. cjrandis. 
Where the current is swiftest, where their abiding places are perhaps the most 
inaccessible, there one is likely to find the larvae of these species. Their 
presence was first noted on the Lamar River, on June 23, when several dead 
larvae were found stranded in a flood pool. Somewhat later, June 28. stranded 
pupae were noted. The first adults were seen July 5, on the rocks in Yellow- 
stone River, “on the shady side of the large boulders in the strongest current, 
gathered in groups of forty or more. Very difficult to secure with a net (dip- 
net). Some drop into the water, and appear to have little difficulty in reaching 
a rock again. Apparently somewhat hydrofuge (notes of July 5).” The 
adults were found from July 5 through the following months. The last were 
observed September 6 (into October in Idaho streams). Pupae were found 
quite frequently during the low water stages, but the larvae only very rarely 
(Figs. 106, 107 and 108). 

Because of their very firm means and methods of attachment one would 
hardly expect to find the larvae and pupae in fish stomachs. Yet they do occur 
in trout food. The adults occur much more frequently among food items of 
fish than do the earlier stages. 

One of the most noteworthy discoveries of the summer was that of a 
Deuterophlebia larva (Fig. 109) in Yellowstone River on July 30. This enig- 
matic larva for several years defied any attempt at identification. Very recently 
its identity was established, through the courteous aid of Dr. Johannsen of 
Cornell University. A detailed account of this new American record has been 
published elsewhere (See Bull. Brooklyn Ent. Soc., Yol. 22, pp. 245-249, 1927). 

Deuterophlebia was described from a pair of male specimens from India, 
which formed the type of a new species, genus and family of Diptera. Several 
years later the larval stages were described by Miss Pulikovsky from materials 
received from the Altai Mountains in Siberia. The Yellowstone River larva 
establishes this genus and family for North America. For the Park there are 
three records : 

[uly 10. Lost Creek at Camp Roosevelt. Pupae taken from sluice-dam. 
Elevation about 6300 feet. 

July 30. Yellowstone River, at Cooke City bridge. One larva caught in 
plankton net. Elevation 5900 feet. 

Aug. 2. Tower Creek Canyon, about four miles above Tower Fall. Pupae 
taken from rocks holding Bibiocephala pupae. Elevation about 6700 feet. 

While the pupae of both families are very similar, the larvae are very 
unlike, as will be seen upon comparison of the figures 106 and 109. Bibio- 
cephala is long and flat, with a series of ventral suckers; its locomotion is 
extremely slow and clumsy. Deuterophlebia has a number of pro-legs with 
terminal pads for attachment; although the locomotion was not observed, to my 


Ecology of Trout Streams 


19 r 


mind the pro-legs operate much like the tube- feet of Echinodermata. The simi- 
larity of the pupae is regarded by Miss Pulikovsky not as indicating relation- 
ship, but as a clear case of convergence, similar to that shown by certain 
Psychodidae. No adults were taken in Yellowstone Park. But I suspect from 
the similarity of habitats and from what Miss Pulikovsky has written that the 
adults probably show similar habits. 

The larvae of Blepharoceridae (and Deuterophlebiidae) are found where the 
conditions of mountain streams are most strenuous, namely, in the strongest 
rapids and behind water-falls. The pupae are found under similar conditions. 
The adults like to sit on rocks, near the surface of the water, where the spray 
keeps the rock continually moistened. 

The third family of Diptera that is confined to rapid waters is the family 
Simuliidae. It is very probable that a number of species are represented in 
the streams of Yellowstone Park. Of the fifty-five blackfly species of North 
America listed by Dyar and Shannon (’27), some eighteen are regional; that 
is, they occur in regions adjacent to Yellowstone Park. In fact, seven of these 
regional species were actually taken in the Park, chieflv at Mammoth Hot 
Springs and Old Faithful. It is very likely therefore that the specimens col- 
lected and observed in the various streams represent more than one species. 

In the Yellowstone the larvae and pupae were quite scarce after the spring- 
flood, and none too frequent in the Lamar. At the same time the small tribu- 
tary creeks and rills contained an abundance of Simulium From observations 
made during the summer it seems that the larger streams are restocked every 
year by specimens from the smaller tributaries. Thus, at the mouth of Elk 
Creek, on July 15, the stones were covered with large patches of Simulium, while 
the Yellowstone showed none of these larvae. About three weeks later the 
river, too, showed an abundance of Simulium just below the mouth of Elk 
Creek. Similarly in Lost Creek at the time of high water (about June 20! 
Simulium was very scarce. On June 19 a small rill leading from the creek to 
the meathouse of Camp Roosevelt was found heavily infested with Simulium 
larvae and pupae. Lost Creek above and below the rill showed few traces of 
the species. Turning the water from the rill for two days dried up the Simulium 
and stopped their appearance at the camp during the summer. As the waters 
of Lost Creek fell, Simulium became more and more abundant and conspicuous. 

In Yellowstone River the larvae were found to contain a considerable portion 
of lake plankton in their food. This was evidently swept downstream from 
Yellowstone Lake, and the larvae combed this food from the waters (Fig. 
no). In turn the larvae and pupae are eaten by fish. Small Pteronarcys 
nymphs were observed feeding on them ; it is also probable that at least Hydro- 
psyche among Trichoptera and the larger mayfly nymphs feed on Simulium. 

A nematode parasite is quite frequent in the larvae. A field note of August 
ir is pertinent: “Yellowstone River. Simulium was found extensively parasit- 

ized. Certain individuals were noted with swollen caudal end and of greater 
length than others. These specimens were invariably pale green on their venter. 
A green Mermis ( ?) was noticed in the net. Comparison elicited the fact that 
all swollen individuals were parasitized. It was not determined whether any 


198 


Roosevelt Wild Life Annals 


pupae were parasitized or if parasitized individuals could pupate. It was evident 
that the Mermis were leaving the larvae for their free-living adult stage. Just 
at what point they left the Simulimn was not established. It was noted, how- 
ever, that the parasite was coiled chiefly at the posterior end of the larva, with a 
small coil near the head.” 

Of families with occasional representatives in mountain streams, the Psy- 
chodidae, Chironomidae, and Leptidae should be noted. A species of Psychoda 
was caught quite freely along the various streams, but none of the larvae were 
found. It is probable, according to Thienemann, that the larvae would be 
found among the deposits on rocks. 

Of Chironomidae the following species were found : Ccratopogon sp., 
Chironomus sp., Cricotopus varipes, Metriocncmius sp., Orthocladius sp.. Pro- 
cladius sp., Tanytarsus exiguus. It is probable that many more species are 
represented ; but since the main attention had to be given to the more dominant 
and conspicuous forms, the chironomid collections were perforce somewhat 
neglected. Cera'topogon larvae were found repeatedlv in the sandv spots in 
Lost Creek, among the accumulations between rocks, and in the marginal areas. 
No pupae were obtained. Cricotopus and Tanytarsus were conspicuous in the 
sulphur and slime deposits on rocks along the shores and in midstream on sub- 
merged rocks. There they gathered and built their tubes by the thousands 
into a flocculent mat, among which rock diatoms and algae thrived. Here, too, 
might be found the Yorticellidae (Hydra also, in European streams). Young 
fish fed on these mats with eagerness ; but larger fish seemed to despise them 
and came to them only when extremely hungry. 

Adult midges could be seen flying along the shores among the grasses or 
into the spray of the lesser and shallower rapids. 

The Leptidae are represented by Athcrix variegata Walker. The larvae 
have a rather wide distribution in mountain streams and are frequentlv found 
in trout stomachs. For the adults. Malloch's account can be quoted 1 p. 363) : 
“The females of the genus Atherix have a peculiar egg-laying habit. The 
eggs are deposited upon branches or twigs of willows or other trees over- 
hanging streams. After oviposition the female does not fly away, but dies and 
remains attached to her egg-mass. The second female adds to the already 
deposited mass both her eggs and her body, and gradually others do likewise, until 
the combined mass of eggs and flies assumes considerable proportions, often con- 
taining several thousand dead flies. The larvae which hatch drop from the mass 
into the stream below, where they pass the immature stages. The Indians in 
Oregon at one time collected the masses of eggs and flies and used them as 
food. An interesting account of this aboriginal utilization of nature's resources 
is given by Prof. J. M. Aldrich (Ent. News, Vol. 23, pp. 159-164).” 

The cluster shown in figure in measured about seven by twelve inches and 
was fastened to the underside of an overhanging rock. The position of the 
rocks is indicated in figures 71 and 112; figure 65 shows the same rocks from 
the distance. The photograph was taken under somewhat difficult conditions, 
since at the time the base of the rock was surrounded by rapids. My notes 
for that dav are as follows: “Flies in cluster arranged in shingle fashion, each 



Fig. 87. Huge boulder in stream bed of Oro Grande River, Idaho. This boulder is 
fully forty feet high. Smaller boulders can be seen on the slope along the river. 
Sept. 2, 1924. 



Fig. 88. Trick Falls, Glacier Park, in Two Medicine River, a short distance 
below Middle Two Medicine Lake. Photograph July 17. 1925. The Same 
place was visited Aug. 26 ; the lower part of the falls, which emerges from an 
underground conduit, was then completely dry. 



200 



Fig. 89. Keppler Cascade, Yellowstone Park. Aug. 
18, 1921. 



Fig. 90. Oro Grande River, Idaho. Freak root's of a tree on top of a boulder. One 
root circles to the left and then turns under the tree. The boulder is surrounded 
by water, and none of the roots passes into the stream bed : the boulder showed 
no sign of being cleft. 


Ecology of Trout Streams 


201 


straddling neighbor in part. All so arranged that at periphery of cluster the 
individuals face outward. Unevenness of rock has caused several whorls. 
Composed of thousands of specimens. All dead. These are this year’s flies. 
Cause of death unknown. Came here for oviposition, for under them a fibrous 
deposit is full of eggs, some of which are hatching. The mass is invaded by 
a number of Tro.v adults, and Dermcstcs, also one or two Staphylinids.” My 
last notation is of August 23 : “Winds and scavengers have stripped the patch 
so that only very few dead Atherix remain. But Dcrmestes larvae are still 
feeding on them.” 

The Tipulidae, too, seem to be represented, for along the shores in the moist 
sand or earth, between rocks, or submerged, one finds tipulid larvae of vari- 
ous types. No attempt was made to collect them systematically, since they 
appeared to be rather infrequent. One peculiar larva collected is shown in 
figure 1 13, taken from Tower Creek, August 29. This larva inflated its pos- 
terior end in balloon fashion ; for what purpose, is not known. 

Diptera are further represented by what I have called “splash flies” or 
“spray” flies. These are the adults of Philolutra simplex and Chamaedipsis 
coniata Melander. They occur in fair numbers on the exposed rocks of streams 
(Figs. 93 and 114). They make short flights to the water surface, alight at 
the immediate edge of the current on the rock, and then run upward through 
the spray. They seem to prefer the shady side of the rocks. Quite generally they 
were mixed with Bibiocephala. Like these, I found them during the entire 
summer, and even later in Idaho streams. The earlier stages are unknown 
to me. Whether they are native forms or merely visitors I was unable to 
ascertain. They are much more numerous than the Blepharoceridae, but despite 
this they are much less frequent in fish stomachs. 

Among casual visitors near the water, Boletma melcncohca, Mycomyia 
mendax, Linanculus qucrulus, Leptoccra sp., Paralimna sp., Empid sp., have 
been identified. It is very probable that many of these breed under moist 
conditions, hence not in the water, but at the margins of streams. 

Insecta. Colcoptcra. — The bettles like so many other aquatic types, are 
practically absent from the mountain streams of the Park. Certain species 
( Hydrobius scabrosus Horn, Agabus tristis Aube, Crenitis monticola Horn, 
Dcronectes griseostriatus DeGeer, and Hydroporus sp.) were found in the 
marginal shallows and pools, especially in the recession pools. The test for 
the true fauna of the mountain streams lies in the food contents of fish stomachs. 
Endemic species will be found there in the larval and adult form. Surface 
drift can be readily distinguished. Thus, the beetles noted above are practically 
entirely absent from the stomach contents either as larvae or adults. In fact, 
one finds them only as adults, if present at all. If one wishes to find the larvae 
of these species one must look to the ponds and small lakes and marshes. 

What surprised me was that the streams did not show anv Parnidae and 
Dryopidae (Figs. 105 and 106), the typical beetles of lake shores. Idaho streams 
such as the Clearwater, the Palouse River and others, in places show an abund- 
ance of Psephenus larvae and occasionally other parnid species. But in Yellow- 
stone Park thev seem to be quite rare. I have one record of a Psephenus 
skin, August ir, Yellowstone River, at Cooke City bridge, “taken from Simu - 


202 


Roosevelt Wild Life Annals 


hum society.” This may have been carried down from Yellowstone Lake. 
Another record was “June 28 — Parnid larva taken from Lost Creek.” This 
was placed in a screened jar with the hope of breeding the specimen. With 
this jar were a number of others, containing various stonefly nymphs, mayfly 
nymphs, and Trichoptera larvae. Unfortunately, as already noted, the bears 
of that region had too keen a scientific curiosity and wrecked my breeding 
arrangements by tipping over the jars, scattering them downstream or removing 
them altogether. 

Shore beetles of various sorts play the parts of scavengers on various 
stranded biota ( Cicindela , Dermcstes, Staphylinidae ; see notation under Trich- 
optera). Another situation was of considerable interest. This was in connec- 
tion with the Atherix cluster described (see Diptera). Although the cluster 
could hardly have been more than a week old at the time of its discovery, still 
the larvae and adults of Dermcstes talpinus Mann, and the adults of Trox sp. 
and several forms of Staphylinidae were feeding on the dead Atherix adults 
and on the developing eggs. 

c. Chordata. Practically all the classes of Chordata are represented in the 
mountain waters and affect its biota either directly or indirectly. 

1. Fish. — The characteristic fish of the mountain streams are the native 
red-throat trout ( Salmo clarkii), which are found in the highest elevations. 
Besides these one may also find minnows, occasional bass, suckers, pea-mouth, 
bullheads, Cottus, and graylings. Cottus has been found at surprisingly high 
elevations; Cottus punctulatus (Gill) is recorded from the Yellowstone, and 
other species from various rivers of the Northwest. The grayling ( Thy - 
mallus) is held by Thienemann as typical of the lower elevations (below 1000 
meters) of rapid streams. In Idaho streams I have found Cottus, bullheads, 
pea-mouths, and other fish at elevations of 3000 feet and less, in the larger 
streams. 

In Yellowstone National Park (and to a lesser extent in Glacier National 
Park) the planting of exotics (non-native fish) in the lakes and streams, includ- 
ing various foreign trout, whitefish, pike, pickerel, rock bass, silver bass, perch, 
etc., has perhaps affected some of the faunal complex, at least of the lakes. 
Records of plantings are not available except for recent years. In places it 
is therefore difficult to tell whether the fish present are native or foreign. On 
the Pacific slopes the upstream migration of the salmon annually affects the 
headwaters of streams. No food is eaten by the salmon, but the spawning and 
the ensuing death, followed by decay of the adults, probably affects the life and 
physiology of the stream in many ways. This is a problem that invites study. 

2. Amphibia. — No amphibia are native to the mountain streams. Frogs 
and in one case a salamander or newt (not captured) were found at points 
where ponds, and marshes occur. Generally the frogs are only visitors to the 
streams, or may have wandered away from their proper habitat. 

On rare occasions one may find frogs among the stomach contents of fish. 
I have only one record of a frog taken as food by trout, in the meadows of 
Slough Creek. As a matter of fact, several attempts were made to use small 
frogs as bait for trout; the fish seemed uninterested and refused it. In turn the 
frogs eat much of the insect life along the streams — stoneflies. caddisflies. beetles, 


203 



Fig. 91. MacDonald Creek, Glacier Park. Just above the falls the stream bed 
consists of stratified rock. Aug. 17, 1925. 



k ig. 92. \ ellowstone River, at Cooke City bridge. Showing rapids and marginal 

pools. Aug. 15, 1921. 


204 



Fig. 93. Yellowstone River showing rocks with “splash flies.” July 7, 1921. 



Fig. 94. Lamar River eddy, showing marginal pools. Later these pools 
became dry. Pool at upper left is completely cut off from stream. In 
the middle the moist bottom of a recession pool shows clearly. July 16, 
1921. 


Ecology of Trout Streams 


205 


etc. The stomach contents of a frog taken along the Lamar showed several 
Acroncitria pacifica, some beetles and flies. 

3. Reptilia. — Snakes are frequent visitors along the shores of mountain 
streams. Garter snakes were noted repeatedly — six on one day, over twenty 
on another — feeding on whatever food good fortune might cast their way. 
Preferably they would feed in places where rocks were heaped, or where such 
rocks were sufficiently close and with spaces between and under them to pro- 
vide proper shelter and good hunting ground. Repeatedly I observed the 
garter snakes catching and eating adult stoneflies (. Pteronarcys , Acroneuria). 

In no way connected with the work was the capture of a “rubber boa” on 
the evening of August 10, along the road between Tower Fall Junction and 
Tower Fall. Dr. C. C. Adams and Dr. G. M. Smith were with me at the time. 
The specimen was sluggish in behavior, very inactive and rather docile when 
picked up. It was later identified as Charina bottac (Blainv.). This species 
is widely distributed along the Pacific Coast. Since then I have seen it in 
Idaho, near Moscow Mountain ; and from descriptions of students, farmers, 
hunters, etc., I find that it occurs throughout Idaho and western Montana. 

4. Aves.— Of birds only one can be called a species of the mountain streams, 
the water ousel or dipper ( Cinclus mexicanus unicolor). This is the character- 
istic bird of the rapids. There one may observe it on exposed rocks, “dipping” 
in characteristic fashion. From time to time it wanders into the water, through 
the rapids, disappearing completely beneath the surface in search of food. Fre- 
quently it emerges some twenty-five or more feet away from the point of entry. 

Along the shores nighthawks ( Chord dies virginianus lies peris) robins 
( Plancsticus migratorius propinquus), and other birds were seen feeding 
on stoneflies. Thus, morning after morning during early July one might find hun- 
dreds of stonefly wings (of Pteronarcys and Acroneuria) gathered in some 
favorable spot, apparently stripped from the insects before they were eaten. 
Although nocturnal observation was difficult, I feel certain that quite a number 
of birds followed the crepuscular flight of the stoneflies and fed on the swarms 
(see stoneflies, p. 189). 

5. Mammalia. — \ isiting mammals are not at all infrequent along the moun- 
tain streams. Most noteworthy are the moose (Alecs amcricamus shirasi Nelson), 
the elk ( Cervus canadensis canadensis Erxleben), mule deer ( Odocoilcus 
hemionus hemionus Rafinesque), White-tail Deer ( Odocoilcus virginianus 
macrourus Rafinesque), various mice, beavers ( Castor canadensis canadensis 
Kuhl), otters ( Lutra canadensis canademsis Schreber), black or cinnamon bears 
( Ursus americanus Pallas), and water shrews (Neosore. r palustris navigator 
Baird). 

Of these the beavers, water shrews, and otters can be said to affect the 
stream life directly, the others more or less indirectly. The bears were con- 
stantly noted along Lost Creek, and Lamar River, plunging in for a bath, ford- 
ing the stream, or perhaps looking for some toothsome fish. Water shrews were 
observed only twice, swimming about actively in search of aquatic insects. The 
beavers affect the smaller streams primarily by damming. The domiciles and 
engineering feats of beavers may be observed at thousands of points along the 
streams of the Northwest. Lost Creek, Carnelian Creek, Lava Creek, etc. are 


206 


Roosevelt Wild Life Annals 


excellent illustrations of dammed streams. Along Tower Creek there are a con- 
siderable number of large springs which have furnished sites for a number 
of beaver works. 

The results of such damming of streams are both direct and indirect. As 
direct results may be indicated the destruction of current for long stretches 
and hence a modification of the streambed and of the constitutive fauna and 
flora. An indirect result is the drowning of adjacent forests, which in time 
leads to the alteration of the stream banks. 

ECOLOGY OF MOUNTAIN TROUT STREAMS 

A. General. In the first part of this paper four types of mountain streams 
were distinguished : the constant streams, the flood or variable streams, the 
precipitous streams, and the temporary hillside streams. This classification does 
not agree with that of Steinmann (’07) for the alpine streams of Switzerland. 
Steinmann recognized two types of mountain streams, (a) the elevated moun- 
tain streams (Hochgebirgsbache), which have their origin from the melted snows 
of elevated fields and mountain sides and from glaciers; (b) middle mountain 
streams (Mittelgebirgsbache), which are fed by springs. The latter might also be 
called valley streams since they traverse the mountain valleys and there gather 
the waters of tributaries. 

Thienemann (’12) notes certain weaknesses in this classification, notably 
the fact that it is based on altitude, and that insufficient distinction is made 
between the major habitats and their subdivisions. Based on the study of 
streams of the lower mountains of Germany. Thienemann adds certain elements 
and offers the following classification : 

A. The springs and their outlets, which are fishless. 

B. The elevated and middle streams, which contain trout. 

C. The lower streams, which contain grayling. 

Springs and rills solely would he found in the higher altitudes. These 
are followed by streams which contain Salmonidae ; these in turn by streams 
in which the Cyprinidae predominate. 

Both Steinmann and Thienemann consider the spring biota as ecologically 
related to those of the mountain streams. While granting a physiographical con- 
tinuity between spring outlets and streams, an ecological continuity appears to 
me to exist only under exceptional conditions. In no place does this become so 
apparent as in Yellowstone Park. Although in the present study the springs 
received little attention, a word about them may not be amiss. After a number 
of reconnaissances of the aquatic conditions in Yellowstone Park I recognized 
the futility of obtaining even to a slight extent a fair picture of the true relations 
of the springs to streams. For the springs of the Park are not only multitudinous 
in number, but also multitudinous in variety One could employ a dozen different 
criteria for their classification and still not exhaust them. One might classify 
springs according to topography, whether their waters immediately fall away after 
leaving the ground or whether they are caught in a pool of varying size ( Born- 
hauser). One could also classify them according to size and temperature; as for 
the latter, the springs range from icy chilliness to boiling point. One might arrange 


207 



Fig. 95. Yellowstone River, rapids and whirlpool, a short distance above 
Cooke City bridge. July 7, 1921. 



Fig. 96. Lost Creek, showing tangles and underbrush along 
stream. Sept. 2, 1921. 



208 



Fig. 97. Spider webs, with prey of aquatic insects. From rocks beside Lost Creek 

Falls. Sept. 2, 1921. 



Fig. 98. Detail of a spider web, showing various insect adults. Lost 
Creek Falls. Sept. 2, 1921. 


Ecology of Trout Streams 


209 


them according to color, which not only differs among different springs, but often 
in the same spring at different times. Again, one could classify them accord- 
ing to substances in solution, such as carbonates, arsenates, chlorides, silicates, 
sulphides, etc.; or according to substances in suspension, such as sulphur, mud, 
sand, silt, etc. In fact, every conceivable type of spring occurs in Yellowstone 
Park and feeds the various streams (see Brues, ’24). 

In the main, the influence of these springs is only a local one, that is, 
circumscribed and limited to a very small area of influence, although at least 
in the Firehole River in the Upper Geyser Basin the temperature and chemical 
composition of geysers and springs modify the river water sufficiently to affect 
the faunal makeup. But all these various factors modify the composition of the 
spring biota and of the plants and animals found in their outlets. 

It was the realization of the great variegation of the springs that quickly 
dissuaded me from attempting to study in detail the relation of the fonticolar 
to the torrenticolar associations. The excellent studies of the fauna of thermal 
springs in Yellowstone Park made by Brues in 1923 indicate many of these 
difficulties of ascertaining this relationship. 

B. Classification of Habitats. Even at first glance it is evident that 
mountain streams, with their major and minor falls, their many winding and 
tortuous rapids and channels, their indescribable intermingling of tumbled and 
placid waters, represent a highly specialized habitat, indeed, the pinnacle of 
aquatic specialization, comparable only with shores of oceans and larger lakes. 
Yet it is also obvious that this biotic unit is composed of simpler associations, 
each with its individual peculiarities. A classification of these must necessarily 
be based partly along physiographical, partly along physiological lines. Thiene- 
mann (’12) offers a classification, with which, as indicated in part II of this 
paper, I am unable to agree. For the sake of clarity the two groupings are here 
placed side by side ; 

After Thienemann. 

A. Types of streams. 

1. Rills and Springs. 

2. Streams. 

a. Elevated streams and middle 
streams, trout streams. 

b. Lower streams, grayling 
streams. 

B. Ecological Habitats. 

1. Springs and rills. 

2. Stream. 

a. Open water. 

b. Bottoms and surface. 

aa. Stone fauna, 
bb. Plant fauna, 
cc. Quiet inlets and bays. 

— on the water. 

— among leaves and dead 
branches. 

— in sand and mud deposits 
(slimes) . 


aiiojuouai, nun v a. 1 

g. Marginal pools. 

h. Recession pools. 


Author’s Classification. 

A. Types of Streams. 

1. Rills and Springs. 

2. Streams. 

a. Constant. 

b. Variable or flood. 

c. Precipitous. 

d. Temporary. 

(Springs and rills) 

B. Ecological Habitats 

1. Permanent habitats, with native 

biota. 

a. White water habitats — falls, 
cascades, white rapids. 

b. Clear rapids and stone bottoms. 

c. Flacid water habitats — pools 
and holes. 

d. Marginal areas. 

2. Interrupted habitats, with native 

biota. 

e. Deposits — on rocks, etc. 

f. Splash areas — on rocks 

3. Temporary habitats — transient and 


210 


Roosevelt H'ild Life Annals 


In the foregoing classification I have tried to recognize the important fact 
that the trout streams have a marked seasonal variation which emphatically affects 
the living organisms. In this respect the mountain streams do not differ from 
other aquatic bodies, which are also affected seasonally, and by the same factor, 
namely the spring floods. 

A further criterion needs stressing. Both Steinmann and Thienemann make 
little distinction between what I have called native or endemic (or primary) 
organisms and invading (or secondary) organisms. Yet I believe this dis- 
tinction requires emphasis. Certainly animals and plants found only in some 
small and isolated locality in one stream and not elsewhere can hardly be called 
endemic ; similarly, insects the larval life of which is spent in quiet water and 
which in their adult stages visit the marginal pools, cannot be called native to 
mountain streams. 

In Yellowstone River, for several miles below the outlet from Yellowstone 
Lake, there occur several species of plants, such as Potamogeton, Myriophyllum, 
and even some tiny patches of floating Lemna. This despite the fair current of 
the stream. But it is only in this locality that these plants occur at all. Farther 
down one never sees such plants. Yet below Yellowstone Falls there are 
considerable placid stretches where one might expect higher plants to effect a 
luxuriant growth ; such, however, is not the case. No plants above the algae 
and mosses have been able to establish themselves. 

Only those species can be said to be native or endemic which can exist 
under the average conditions offered by the particular ecological region. For 
ecological clarity, this distinction between what is primary and secondary, 
between what is native and what is foreign, between what is of constant and 
year round occurrence and what is temporary or transient, must be recognized. 
If not, then there is no purpose in ecological study of any sort, since then a 
sporadic or single occurrence would be of equivalent value to constant and 
wide-spread occurrence. 

Quite logically it may be asked : Is there a criterion by means of which 

we can judge what life is endemic and what is foreign to mountain streams? 
Fortunately there is such a test which to a marked extent permits one to sep- 
arate the native from the foreign biota. This criterion is the food, hence 
the stomach contents, of trout and other fish. Perhaps the food of stream 
insects should be considered also, since insects, aside from fisb, constitute about 
98% of the bulk of the stream fauna. At any rate, endemic species will be 
found quite regularly among the stomach contents and represented by both 
their larval and adult stages, or at least the larval stages; transients will be 
found only intermittently and as adults. 

C. The Habitats. (Springs and Rills). As already noted, springs and 
tbeir outlets received scant attention in this study. While physiographically con- 
tinuous with mountain streams, they are physiologically separate. The follow- 
ing is summarized from Thienemann and Bornhauser. Bornhauser (’13) in a 
special study of springs groups them into two types — limnokren and rheokren. 
Rheokren are those springs from which the water flows away at the mouth. 


211 



Fig. 99. 


Pteronarcys ccilifontica nymphs on rocks, “emerging 1 ’ 
from their nymphal skins. July 25, 1921. 



212 



Fiji. ioi. Cluster of Acroneuria adults in crevice of rock. Yellowstone River. 

July 6, 1021. 



Fig. 102. Stoneflies {Acroneuria) mating on shore grass along Yellowstone 

River. July 6, 1921. 


Ecology of Trout Streams 


213 

down a hillside; there is no trace of any pool, just a direct outflow. Limno- 
kren are springs which have a pool of varying size (Fig. 79). As characters 
for springs Bornhauser notes (a) constant renewal of “filtered," and hence 
“fresh” water, and (b) constant and low temperature. These two characters 
may be affected by altitude, age, the plants, temperature, environment (e. g., 
woods, open field), and food supply. 

Thienemann ('12) classifies the fauna into three groupings for springs: 
(a) animals that are subterranean, (b) land forms and “moisture friends,” 
(c) true spring forms. Bornhauser recognizes further distinctions among these 
types and groups them as follows: (a) Strange or foreign elements, (b) cosmo- 
polites and ubiquists, (c) stream forms, (d) alpine forms (profound and 
boreal), (e) true spring forms, and (f) subterranean forms. 

In the rills (Fig. 63) formed by spring outlets the fauna, according to 
Thienemann. agrees with that of the more quiet portions of mountain streams, 
i. e., that of the deposits and pools. From a physiographical standpoint such 
spring outlets are distinguishable by the stones which for the greater part are 
not submerged, but only moistened at their bases. Where such rills and outlets 
enter the stream proper, there one finds the repositories of trout eggs. 

1. Permanent Habitats. These are the habitats which exist throughout the 
year, which neither the spring floods nor the summer droughts can extinguish. 
The same biota may be found here throughout the year. Mingled with it at 
times, chiefly at low water stage, one may find a foreign element, but such 
intrusion is rare. In these habitats the typical life of the mountain stream is 
found. 

a. White Water. — Here are included the falls (Figs., 68, 74 and 88) r 
cascades (Figs. 62, 66, and 89) and white rapids (Figs. 66, 68, 84 and 95) 
recognizable by the flow and color of the water. In falls the flow of the current 
is vertical, in cascades oblique, while in the white rapids it is a mixture of 
vertical, oblique, and horizontal flows. In falls and cascades the current flows 
chieflv in one direction ; in white rapids the current is twisting, whirling, tumb- 
ling, hence simultaneously of many directions. Physiologically, one must note 
pressure and impact. Pressure arises from the volume of the water ; impact 
refers to the force with which this volume strikes an opposed obstacle. As a 
result of the impact the water becomes white in color; this is merely the white- 
ness of the foam and of the air in solution. The water here is thoroughly 
saturated with oxygen, indeed, is really supersaturated. Impact and whitened 
waters, and hence a lack of transparency, are the more obvious characteristics 
of white water habitats. 

Under such extreme and violent conditions one would hardly expect to 
find anything living at all. Yet curious to say, directly behind the falling 
water, and sometimes in the midst of it, if the volumes of water are not very 
large, one may find moss and bits of Cladopliora caught in tiny crevices. In 
similar situations I have found Blepharoceridae larvae and pupae, and also the 
pupae of Deuterophlebia (Figs. 106 and 107). The distinct dorso-ventral 
flattening of the larvae and pupae, the powerful suckers which serve for attach- 
ment, and the very slow locomotion can be recognized as excellent adaptations. 


214 


Roosevelt Wild Life Annuls 


Where large rocks extrude from the white rapids and are dashed with 
spray one also finds the adults of several species of Diptera running up and 
down the rock or sitting quietly in the spray (Fig. 114). These are the adults 
of Blepharoceridae, Chamaedipsis and Pliilolntra (Figs. 93, 108 and 114). 

b. Clear rapids. — The clear rapids (Figs. 57 and 78) are distinguishable 
by the steadier flow of the water, the lack of opposed obstacles, and the trans- 
parency of the water. Typically they have a bottom of rounded, water-worn 
stones. An acoustic distinction might also be noted. Thus falls have a note of 
thunder, a deep bass ; cascades have an overtone as of something rushing by : 
white rapids have a tearing, ripping sound ; while the clear rapids have a 
laughing, bubbling tone. 

This is the typical habitat of the mountain streams. Here the plants may 
find a hold on the immersed rocks. Here Cladophora, Prasiol a>, and Nostoc 
thrive. Here also Oscillatoria and Melosira may form films on the rocks, in which 
various rock diatoms grow abundant. Here, too, Thremtna becomes prominent 
among Trichoptera, crawling about on the rock surfaces; while Rhyacophila 
and Brachycentrus fasten their cases in numbers on the upper surfaces of the 
rocks (Figs. 104 and 105). Behind and beneath the stones a luxuriant fauna 
and micro-flora appears. Ulothrix, Melosira, Oscillatoria, etc. form clumps in 
which smaller micro-organisms may establish a circumscribed residence. Blepha- 
roceridae larvae (probably also Deuterophlebia) wander freely all over the 
stones. Groups of Trichoptera such as Hydropsyche, Philopotamus, Goera, etc. 
foregather between and under the rocks ; flatworms such as Polycclis and Dcn- 
drococlium lay their slime trails and feed on the micro-life; mayfly nymphs 
such as Heptagenia, Ecdyurns, Iron, Ephemerella, Bactis hunt diligently; and 
Acroneuria among stonefly nymphs finds this the optimal hunting-ground. 

Here, too, trout of medium size like to establish their feeding ground, eat- 
ing whatever the currents bring them, or picking suitable food off the rocks. 
Occasionally they will make quick forays into the white rapids. In precisely 
this sort of habitat I found bullheads in the Clearwater River in Idaho (opposite 
the mouth of the Wietas River) ; similarly in Glacier Park, in MacDonald 
Creek, just above its junction with the Flathead River, I observed Cottas. 
Suckers, too, may be found on rare occasion. 

Where stones come sufficiently close to the surface, Siniulinm may settle 
and thrive. A thin film of water flowing over them seems their ideal require- 
ment (see Thienemann, fauna hygropetrica). Where stones extend above tbe 
surface especially the larger stones, the adults of Blepharoceridae. etc., form 
the splash or “spray fauna” (Figs. 108 and 114). 

All of these forms show some sort of adaptations. Either they are dingers 
in structure or by means of their housings, or they are strong swimmers. The 
dingers are quite generally flattened dorso-ventrally ( Polycclis , Dcndrococliuni. 
Iron, Heptagenia, Acroneuria. etc.), or their housings are attached (webs of 
Philopotamus, Hydropsyche, cases of Brachycentrus, Rhyacophila, etc.). The 
swimmers are more cylindrically built. Perhaps to call them “darters" would 
be more appropriate. For no animals truly swim in these rapids. Mostly, they 
hover behind some rock out of the way of the direct current, and dash or dart 


Ecology of "Trout Streams 


- T 5 


forth quickly for the next promising shelter. This is the method of the young 
trout, also of older trout, of bullheads, of insects such as Callibaetis among 
mayflies, Pteronarcys among stoneflies. 

c. Placid Water. — Where a depression occurs in the stream, the water 

tends to become placid (Figs. 58 and 82). The depression may be in the center 
or the side of the stream ; it may be shallow, or very deep, but always dis- 
tinctly beneath the average level of the stream. Usually the depressions are 

lined with rocks, quite generally larger in size than those in the clear rapids. 
These rocks become covered with deposits of various types of sediment after 
the spring floods, although the spring currents do not always wash them away 
entirely. Physiologically, there are the following conditions : quiet water, except 
for the surface current which is strong but smooth ; because of this quiet there 
is less need for attachment ; there is consequent liberty of locomotion. The 
temperature and the oxygen content are the same as in the clear rapids. 

The plants of the pools, except for the tiny algae and diatoms noted in 
the clear rapids, are negligible. Despite the lack of deeper currents, there are no 
submerged or emergent plants. Among animals we find the larger fish seeking 
these pools which afford them freer movement. Of Crustacea there is Cambarus 
(found only in lower elevations, not in Yellowstone Park streams), Pteronarcys 
calif ornica (Fig. 99) and the smaller stoneflv nymphs. Occasionally one finds 
a rare ostracod and perhaps even a cladoceran or copepod. Among Protozoa 
the Vorticellidae find this an ideal environment, and may be found plentifully 
on the rocks. Thienemann lists various species of Hydra for such pools. I 
did not find any, probably because I failed to look for them. Caddisworms 
and mayfly nymphs are uncommon in the pools ; but the smaller stoneflies 
and the large Pteronarcys seem to frequent the pools in preference to the 
more turbulent localities. 

d. Marginal Areas. — Here the shores are referred to. The current is 
lateral in such places, with considerable friction by floating debris. Little bayous 
or inlets are sometimes formed, whose inhabitants are in part typically that 
of the clear rapids, in part that of other aquatic communities (springs, ponds). 
Surface skimmers prefer such areas. In streams of lower altitudes in Idaho 
I have found leeches, annulates (probably a Limnodrilus, sometimes a Gam- 
rnarus or a Hyalella, and Hydroptilidae among Trichoptera in these shore 01- 
marginal areas. In addition, the moist soil affords abiding places for various 
surface breathing larvae, as of Tipulidae, Leptidae, Coleoptera, etc. 

2. Interrupted Habitats. This division is admittedly arbitrary. It is 
characterized by being seasonal. While the habitats noted thus far may be 
found at all times of the year together with their biota, those falling under the 
present head are wiped out completely by the spring floods and must be repopu- 
lated or recolonized every year after the recession of the floods, when the 
currents are less violent. In fact, even during low water stages, during a 
summer freshet, a temporary flood of a few inches may wipe out the deposits. 
An interrupted existence is therefore characteristic of these habitats. 

e. Deposits. The deposits on rocks (Figs. 71 and 83) and bottoms, and 
along the shores are formed by sediments after the spring floods. These sedi- 


Roosevelt Wild Life Annals 


216 

ments may be of varied composition, such as sand, mud, sulphur, etc. The 
spring floods remove these deposits completely, scouring the rocks until they 
are completely cleaned. As the floods recede, the deposits accumulate and the 
fauna is restocked in such places. Because of this annual interruption one 
can hardly speak of a resident fauna. Yet an abundance of smaller chironomid 
species establishes itself in these deposits together with most of the representatives 
of the micro-life noted under the clear rapids. 

For European streams Thienemann notes the regular moss caps on the 
rocks, which during the spring floods are deeply covered with water, but emerge 
partly or completely during the summer droughts. In these moss caps may be 
found many Chironomidae, less motile types of mayfly nymphs, Trichoptera, 
Tipulidae larvae, Athcrix larvae, the free living stages of parasites, Hydra- 
clmida, etc., in fact a fauna that requires considerable protection and which 
can not exist in the mountain streams unless such protection (namely the moss 
caps) is present. In Yellowstone Park such moss caps occurred only in a few 
places along the Lamar (Fig. 72) ; in Idaho the Palouse River contains many 
such moss caps. In both places the fauna was much as described by Thiene- 
mann. Yet since these moss caps are rather the exception than the rule in 
the mountain streams of the Northwest, I am inclined to consider the biota as 
not truly native. 

f. Splash Areas. — Like the deposits, these, too, are interrupted by the 
high water. They are the rocks that protrude from the water and are con- 
tinually moistened by the spray. In this spray certain adults of Diptera ( Bibio - 
cephala, Philolutra, Chainaedipsis) run up and down, fly to the water's edge and 
then run up into the spray (Figs. 93. 108 and 1 1 4) . 

3. Temporary Habitats. These are habitats characterized by an invading 
fauna and flora. They can be regarded as both transitional and transient. — 
transitional as regards the type of organisms found, and transient as regards 
their existence. They are discontinued during high water or low water periods. 
The spring floods invariably wipe them out, and great recession of water will 
do the same (Figs. 54, 65. 71, 72, and 83). Perhaps no stream showed the 
relations of the regressive migration of the stream fauna together with the 
progressive invasion of foreign biota so typically as did the Lamar River. As 
the spring floods receded, sand was deposited copiously in the shore areas 
among the stones. In many places there were small pools and minor rapids, 
all connected by trickles (Figs. 75 and 76). The inhabitants migrated toward 
the deeper parts of the stream if possible; others, especially attached forms 
( Rhyacophila, Rrachycentrus ) became stranded or at least isolated: simultane- 
ously, these pools became populated w T ith various beetles, occasional Flemiptera 
( Corixa , Notonecta) , copepods, Cladocera. and also various filamentous algae 
( Spirogyra , etc.), all of which are pond types. These pools were mosaic in 
their makeup; that is. only a few representatives of the pond communities were 
present in each pool ; in fact, the pools differed strikingly among themselves. 
Later still, these recession areas dried up completely (Figs. 71 and 72) and 
various shore forms and scavengers appeared. 


21 



Fig. 103. Adult mayfly with a parasitic worm ( Mermis sp.?) emerging from 
the caudal end. Enlarged eight times. Note the loop formed by the parasite 
within the abdomen of the insect. From confluence of Lava Creek and 
Gardiner River. Aug. 4, 1921. 



Fig. 104. Stranded caddisworms ( Brachyccntrus and Rhyacophila) . 
Lamar River. Aug. 8, 1921. 






Fig. 105. Attachment of Brachycentrus cases. Some attached 
at caudal or small end others at broad or "mouth” end. 
Lamar River. July 25, 1921. 


106. Larva of Bibioccphala. enlarged 6 times. Note ventral suckers. 1 -rom 
Snake River, Idaho. At right, pupae of Bibioccphala, showing variation in 
size and ventral attachments. 




219 



Fig. 107. Bibioccphala pupae. From Lamar River. Note the tubes of 
chironomids (T any tarsus?) on the same rock. July 16, 1921. 



Fig. 108. Bibiocepliala adults as “splash flies." Oro Grande River, Idaho. 

Sept. 3, 1924. 


220 



Fig. 109. Deuterophlebia larva. Yellowstone River. July 30, 1921. 



Fig. no. Simulium sp. "Combs’’ of larva. xbO. 



Ecology of Trout Streams 


221 


g. Marginal Pools. — The foregoing described (h) the recession areas. 
The marginal pools can he primarily distinguished by their lateral connections 
with the stream proper. Generally there is some small trickle that leads into 
the pools (this includes the inlets or havous of Thienemann), or there may he 
a broad lateral opening. At any rate, the current does not enter directly ; hence 
there is a certain amount of quiet which permits less well adapted forms to 
establish themselves. These are primarily species of the lake shores, springs, 
and slow rivers. The fauna and flora can be called transitional, and is made 
up of elements from rapid streams as well as the other aquatic bodies noted. 
This is most notable in the types of Chironomidae, Trichoptera, and mayflies 
that establish themselves, but most typically by the surface skimmers that hunt 
in these spots. 

The transition from stream to pond becomes marked in the various beaver 
ponds, especially where these engineers succeeded in damming some mountain 
creek. Such beaver ponds (Fig. 73) contain a rather sparse fauna, together 
with scattered pond plants. Among the animals, Lestcs, Enallagma, and 
Aeschna among Odonata; various beetles; swimming Trichoptera (Triaenodcs) ; 
Notonccta and Corixa among Hemiptera ; and various semiaquatic Diptera are 
present in varying numbers. As a rule, the heavers keep the ponds too well 
cleaned to permit a rich pond life to establish itself. But at least some of 
the types are represented. 

D. Adaptations to Mountain Stream Life. The difficulties of mountain 
stream life necessitate manifold adaptations on the part of the inhabitants. 
Steinmann in his earlier paper (’07) has outlined these so thoroughly that I 
can do no better than repeat them, with added instances. He lists seven types of 
adaptations : 

1. Dorso-ventral flattening. — By appressed structure, as found in Turbcl- 
laria, leeches, Ancylus, stoneflv nymphs, mayfly nymphs (Iron, Hcptagenia, 
Ecdyurus). Many cases of Trichoptera ( Goera , Molanna), Chironomus 
( Tany tarsus) . Egg masses may he laid flat. The cocoons of leeches are flat. 
Pupae of Blepharoceridae and Deuterophlebiidae also are very flat. 

2. Enlargement of adhesive surfaces, e. g., Iron, other Ephemeridae nymphs. 

3. Small body compass, tendency to dwarfing. Noticeable only in plants. 

4. Attachments: Temporary and permanent. Permanent: with cases, 

Brachycentrus, Rhyacophila, Thremrna, Glossosoma, Goera, etc.; without cases, 
Simulium, leeches, snails, larvae' of Blepharoceridae, etc. Temporary, by means 
of suckers, hooks, and anchors: various larvae of Diptera, Trichoptera, etc. 

5. By weighting: web-spinning Trichoptera ( Hydropsyche , etc.). 

6. Reduction of swimming hairs, which are reduced in number or 
degenerate entirely. 

7. Respiration. No surface breathers present. 

Thienemann also notes an adaptation to temperature, namely the fact that 
the Acarina of mountain streams lay fewer, but larger eggs. 

To this I would add a final adaptation in habit, namely that of the food eaten: 
the diet of inhabitants of mountain streams becomes generalized. Elsewhere (see 


2 22 


Roosevelt Wild Life Annals 


Muttkowski-Smith) this has been formulated as an axiom: the more specialized 
the conditions of the habitat, the more generalized the diet; the more generalized 
the conditions of the habitat, the more specialized the diet. 

Dodds and Hisaw (’24 and ’25) in their fine studies of the adaptations of 
insects to swift currents, reach conclusions similar to those of Steinmann and 
Thienemann. 


FOOD RELATIONS 

1. Trout Food. To arrive at a proper valuation of the stream population it 
was necessary to examine the stomach contents of the fish. In the following 
pages the stomach contents of a considerable number of trout are listed in tabular 
form. From the contents, an estimate of which is given in cubic centimeters, the 
bulk of the various food items may be inferred. To aid in this, the number of 
specimens of a species eaten is also listed. 


Table No. i. — Showing Food of Trout (Salnio clarkii ) from Yellowstone 

River. June 28, 1921. 


Number 

I 

234 

5 

6 

7 

8 

9 

10 1 1 

12 13 14 15 16 

Contents in cc. . 

20 

2 1 4 12 

5 

25 

7 

4 

2.5 

1 7 

5 2 4 5 10 

W ater Bait 










Limnephilus . . . 

20 

■ ■ 3 i • ■ 

5 

20 

3 

3 

1 

2 

.... 44. 

Rhyacophila. 


...... 






4 

...... 

Hydropsyche. . . 







1 


2 I 

Pteronarcys .... 

I 



2 



1 



Aeroneuria .... 

3 

2 3 4 


16 

2 



6 

4 2 53 

Baetis 

I 




2 



I 


Ephemerella . . 


1 . . . . 

4 



4 

4 

I 


Drunella 




2 




4 

I 

Blepharocera 1 








5 20 

3 

Nematodes. . . 



20 







Tipulid lv 





I 





Surface Bait 










Formica ad 

I 








1 1 

Lg. red ant . 


.... I 








Sm. black ant.. 


.... 6 





1 



Vespa 


.... I 








Bee 



I 







Simulium ad. . 









........ I 

Culicid ad . . 






7 




Plecia ad 

• • 

• • 1 1 3 

I 

3 

3 

2 

20 


15 9 30 

Mayfly 



I 


2 





Cicada ad 





I 




. . 1 . . . . 1 1 

Lucanid ad . . . 


■ ■ 1 • • 








Coccinellid ad. . 

. . 

. . . . j 2 








Cerambycid ad . 


. . . . I 


I 






Hydrophilid ad. 



I 



1 



. . . . 

Scarabaeid ad . . 


...... 

I 






.. .. .. .. .. 


Ecology of Trout Streams 


223 


Table No. 2. — Showing the Food of Trout ( Salmo clarkii ) from Yellowstone 

River 


Number 

June 29, 1921 



June 30, 

1921 


I 

2 

3 

4 

5 

6 

I 

2 

3 

4 

I 

5 6 

7 

Contents in cc 

30 

30 

7 

4 

10 

7 

40 

15 

3 

6 

4 1 

6 

Pteronarcys lv 

I 

3 










I 

Acroneuria lv 

28 

23 

8 

4 

16 

6 

4 

8 

I 

6 

4 2 

I 

Ephemerella nvmph 



4 






5 

I 


3 

Rhvacophila lv 



I 


I 

3 



I 




Limnephilus 






2 







Formica ad 

I 


I 










Plecia 



I 

8 

2 

20 







Lvmpvrid ad 




I 









Hvdropsyche lv 










4 



Black ant 









I 

I 



Simulium ad 









I 

I 



Culex ad 









I 

I 



Plecia ad 









44 

4 



Leptid ad 










I 



Muscid ad 










I 




Table No. 3. — Showing the Food of One Trout Taken from Yellowstone 
River, July 6, 1921 by Mr. A. G. Whitney. Contents About 25 cc. 


Pteronarcys larva 

Acroneuria larva 

Acroneuria adult 

Mayfly adult (Ameletus) 

Platyphylax ad 

Simulium ad 

Winged ant 

Sawfly 

Ichneumon 


I 

4 

10 

20 

1 

1 

6 

I 

1 


Plecia 

Muscid ad 

Lucilia. ad 

Enellagma female ad 

Raphidia ad 

Capsid ad 

Cerambycid ad 

Scarabaeid ad 

Lampvrid ad 


30 


1 

1 

1 

1 

1 

1 

1 

1 


Table No. 4. — Showing Food of Small Trout and Minnows from the 

Lamar River, July 7. 1921. 


Trout 

T 3 .— 

1 4 

2| in. long 








I 

Minnows 
J-2| in. long 

Number 

I 

2 

3 

4 

5 

6 

7 

8 

9 

10 

1 1 

12 

I 

2 

3 

4 

5 

Ameletus sp. small 

1 


I 

4 


I 

1 

I 

I 

I 

I 

I 






Chironomus lv 





I 

I 

1 

I 

I 

I 

I 

I 






Alloperla sp 


I 








Ameletus sp 













I 

I 

I 

I 

I 

I 

I 

I 

Chironomus sp 






























22 4 Roosevelt Wild Life Annals 

Table No. 5. — Showing the Food of Cutthroat and Rainbow Trout from 
the Yellowstone River. July 13, 1921. 



I 

2 

3 

4 

5 6 

Pteronarcys lv 


5 


1 


Pteronarcvs ad 

IO 

2 


2 .... 

Acroneuria lv 





— 4 

Acroneuria ad 

2 


2 


.... 2 

Alloperla ad 

I 





Bibiocephala ad 



4 


2 2 

Ameletus lv 





.... ^ 

Limnephilid ad 

I 


2 



Black ant 

I 




I I 

Green bee 

I 





Cicada 


3 




Cerambycid ad 





. I 

Wood chunks 


4 




Young trout or sucker 







The wood chunks were respectively 1x2x5 an< J 2 x 3 x 4 cm. The young 
fish eaten by number 7 was six inches in length. 


Table No. 6. — Showing the Food of Native Trout from Yellowstone River 
at Mouth of Elk Creek. July 15, 1921. 



Number 3 had a copepod gill parasite. 



Fig. hi. Athcri . r cluster. Lamar River. July 22, 1921. The insert shows a section 

of the cluster enlarged X4. 



Fig. 1 12. Rock where Athcri . r cluster had formed, on underside in cleft of 
rock. Lamar River, Aug. 7, 1921. On July 22, when the cluster was 
photographed, the sharp edge running from left to right was about twelve 
inches above the rapids. 


226 



/ ; - 

Fig. 1 13. Tipulid larva, with inflated “baloon” at posterior end. Tower Creek. 

Aug. 29, 1921. 



Fig. 114. “Spray flies” ( Chamaedipsis and Philolutra ) on rock 
in rapids. Lamar River. Aug. 31, 1921. 


Ecology of Trout Streams 


227 


Table No. 7. — Showing Food of Trout from Yellowstone River at Mouth 

of Elk Creek. July 16, 1921. 



I 

2 

3 

4 

5 

6 

7 

8 

9 

10 

11 

12 

13 

14 

15 

16 

Pteronarcys ad . . . 
Acroneuria ad ... . 
Acroneuria lv . . 

2 

2 

5 

5 

1 

2 

I 

I 

5 

4 

4 

1 

3 

5 

5 

3 

4 

1 

1 

3 

I 

5 

1 

3 

2 

2 

1 

2 

2 

2 

1 

Hydropsvche lv. . 
















Hydropsyche pupa 
Hvdropsvche ad. . 






















6 









Ameletus ad 



I 

I 







1 

1 





Chironomus pupa. 














Plecia ad 

I 

I 










4 





Tipula ad 















Tipula pupa 






I 

I 

I 










Pentatomid ad . . . 
















Cicada ad 
















Cerambycid ad . . . 
Scarabaeid ad. . . . 

I 




I 


















I 

1 






Black ant 



4 





8 







Red ant 






5 









Argynnis ad 





I 











Attid spider 




I 




























One of the specimens showed a Copepod parasite adhering to a gill. 

Another contained a Nematode in its stomach. This may have been taken 
in with food or as a free-living stage of the parasite. 

Besides the sixteen specimens noted above, twelve others were noted for 
their food content. In all cases the food comprised the two species of stone- 
flies. One specimen showed an adult Lestcs sp. 


Table No. 8. — Showing the Food of Trout from the Yellowstone River, 
July 17, 1921. Numbers i-ii from Foot of Hot Springs Near the 
“Needles,” Numbers 12-16 Near Mouth of Elk Creek. 



I 

2 

3 

4 

5 

6 

7 

8 

9 

10 

II 

12 

13 

14 

15 

16 

Pteronarcys ad. . 




I 

4 

2 

4 

I 

3 

1 

4 





2 

4 

3 

7 

1 

3 

1 

5 

2 

6 

Acroneuria ad ... . 

I 

2 

500 

3 

5 

I 

2 

3 

Tipulid ad . 

I 

I 















Chironomus pupa. 
Cicada ad . . 


















1 








I 

I 





Ant 









I 






Sawfly . . 














Enallagma ad . 




1 












Carabid ad 












1 




















Number 2 contained a huge number of adult caddisflies, approximately 
500 specimens. 


228 


Roosevelt Wild Life Annals 


Table No. g. — Showing Food of Native Trout from Yellowstone River at 
Hellroaring Gap. Numbers i-io Collected by Mr. A. G. Whitney, 
the Others by Various Fishermen. 






Ji 

LY 21 , I92I 




July 23, 1921 


I 

2 

3 

4 

5 

6 

7 

8 

9 

10 

1 

2 

3 4 5 

Pteronarcys ad 

4 

6 

3 

2 

I 

4 

3 

2 

8 

5 

12 

8 

4 2 1 

Acroneuria ad 

3 

4 

2 

I 

I 

I 

1 

2 

4 

3 

4 

10 

2 ... . 3 

Noctuid moth 



I 











Hydropsyche ad ... . 






I 





















. ... J .... | 


July 2 4, 1921. Lamar River. Trout collected by Mr. Henry Lambert. 
Three specimens, each with one minnow in stomach. No other contents. 

July 25, 1921. Yellowstone River. Trout collected by fisherman. Two 
specimens noted, each containing a minnow. 

August 1, 1921. Yellowstone River, at Cooke City bridge. Three trout 
noted feeding on caddises of Rliyaeophila. 

August 1, 1921. Lamar River. One native trout with two Doroncuria and 
two grasshoppers. 

August 8, 1921. Lamar River. Two trout, each with two grasshoppers. 

August 11, 1921. Yellowstone River. Trout taken by Mr. Arnold 

V hitehouse at hot springs near the “Needles.” 



I 

2 

3 

4 

5 

6 

7 

8 

9 

10 

1 1 

12 

Ameletus lv 

3 

3 

2 

3 

2 

2 






I 

Caddises 






Acroneuria lv 








I 

I 



Grasshopper 




I 

2 

2 

I 

I 

1 









August 11. 1921. Slough Creek. Two specimens gathered by Mr. Robert 
Hallenberg, one containing a field mouse, the other a green frog. 

August 13, 1921. Yellowstone River. Two specimens collected by 

fishermen, one containing 3 Ameletus and 10 Siviulimn larvae, the second with 
about 200 Simulium larvae. 

These 148 stomachs represent only a portion of those examined, probably 
about one third. Since the others were practically identical as to their contents 
it was not considered worth while to list them all individually. Toward the 
middle of the summer only such specimens were noted as had fed on unusual food, 
such as mice, frogs, pieces of wood, or on one type of food primarily. 

From the listed data it will be seen that it is possible to follow the summer 
history of the fish food, beginning with the spring floods, the summer lapse, 


Ecology of Trout Streams 


229 


and the autumnal re-stocking of the streams. The general history has been 
outlined in an earlier paper: “The Food of Trout in Yellowstone National 

Park’’ (Muttkowski, ’25). Certain conclusions offered in that paper are rela- 
vant and are quoted here: “From the examination of fish stomachs it is possible 
to deduce much about the food habits of fish. First, fish will take food that 
is easily captured ; secondly, that which is accessible with difficulty ; and lastly, 
strange and unusual food. Of the food available in mountain streams, stone- 
flies and mayflies are most easily obtained and constitute the major portion of 
the food eaten. Here, too. the' eggs, fry and fingerlings should be listed, as 
fish are cannibals when opportunity offers; and trout are no exception, hut 
will eat other fish just as greedily as will bass. Caddisflies, well protected by 
virtue of their tough attached cases, and moreover, even more inaccessible on 
account of the appressed structure of many cases, rank in the second category, 
and for that reason constitute a much smaller item of fish food than the other 
two groups of insects. However, they are used extensively as food by the 
stoneflies and mayflies, and in this respect become as important, though 
indirectly so, as their enemies. Among strange and unusual food? can be listed 
the surface bait. 

“In general, fish are opportunists as far as their food is concerned. They eat 
what animal food is available, regardless of the origin. As a result, if one knows 
the animal life of a particular region, one can tell from the stomach contents 
where a fish has fed. In a lake, for instance, the plant and animal life is dis- 
tributed in regular ‘zones,’ most animals limiting themselves to particular depths. 
Some are found only on the shores, others on the vegetation in the shallows, still 
others, only in the muck at considerable depths. With a knowledge of the animals 
found in these various zones it is possible to learn a good deal about the food 
habits of a fish, his migrations, and his preferences. 

“On the whole, fish are indiscriminate in their choice of food as far as 
quality is concerned. They like to feed in a particular region, and stay there 
until satiated. Thus, when feeding from plants, they eat whatever they can 
find there ; and once they begin to feed from plants they continue feeding there 
until their hunger is satisfied. At periods of plentiful food, fish do not migrate 
while feeding. 

“Curious to say, it often happens that a fish may find a certain type of 
food so much to his liking that he will seek only that type. This may be worms, 
leeches, snails, back swimmers, caddis-worms, or other kinds. Thus, we mav 
find stomachs filled with dozens of individuals of one type of animal, such as 
crayfish or snails. Even more striking, one may find stomachs filled with highlv 
distinctive cases of some particular species of caddis-worm. 

“This predilection for some particular food is more often observed in the 
case of surface food than in water bait. I have found fish stomachs, including 
trout stomachs, gorged with hundreds of specimens of a single type, such as 
ants, grasshoppers, dragon flies, caddisflies, orl flies, mayflies, midges, etc., 
indicating that the particular fish had taken a fancy to this special type of 
food, and had hunted assiduously for the delicacy. There is nothing abnormal 
in such a predilection, not more so than in the case of a boy who makes a meal 


- 3 ° 


Roosevelt Wild Life Annals 


off desserts, be it ice cream, or fruit, or cake. But right there, in the longing for 
the unusual, lies the weakness of the feeding habits of fish, the trait which lays 
them open to capture by the angler. Since the unusual attracts, anglers have 
made use of this phenomenon in the types of flies selected by them. 

“A fish is easily deceived, for he is not very observant. His eyesight is 
poor and he recognizes things chiefly through their movements. For instance 
when an angler uses a fly, the fish is supposedly deceived by three factors, — 
form, pattern, and movement. In the matter of form and pattern the fish’s 
vision is too weak and nearsighted to recognize the bait for what it is. He 
is used to certain distorted images which impress him more through motion 
than by any other factor, and he captures or tries to capture such a moving 
object. But it is also the unfamiliar, the unusual, which tempts fish, perhaps 
more than the customary objects. How else can one explain the presence of 
blocks of wood, of straws, twigs, leaves and the like, in fishes’ stomachs? 
On more than a dozen occasions I have found blocks of wood in trout stomachs. 
In at least half the cases there was not the remotest resemblance in the shape 
of the block to any type of surface bait. An irregular cube has no resemblance 
to any insect, while an oblong bit might well have the approximate outline 
of a stonefly or a grasshopper. But it was probably the strangeness, the unusual- 
ness of the block of wood which attracted and tempted the trout. The most 
interesting feature of these instances was that in only one case were the blocks 
of wood taken by a hungry fish ; that is. only once were the blocks of wood 
the sole stomach content. In all other instances, blocks and sticks were gulped 
by fairly well-fed fish. One might say that they were taken as a sort of 
salad or dessert, indicating that their novelty tempted the fish." 

2. Insect Food. A special study of the food of the insects was made 
possible by the collaboration of Dr. Gilbert M. Smith, then of the University 
of Wisconsin, who arrived early in August. Specimens were obtained from 
each of the four type streams and their stomach contents studied, Dr. Smith 
identifying the plant organisms and the writer the animal life. The results of 
this particular collaboration are published in a separate paper (Muttkowski- 
Smith : The Food of Trout Stream Insects in Yellowstone National Park, 

Roosevelt Wild Life Annals, Yol. 2, No. 2). 

For the purpose of the present paper the following may be noted from the 
summaries given in the collaboration : 


Ecology of Trout Streams 


231 


Table No. 10. Showing the Summaries of Food of Trout Stream Insects. 

Yellowstone Park, 1921. 


Name 

Number of 
specimens 

Animal food 

% 

Plant food 

% 

Detritus 

% 

Perloidea 





— Pteronarcvs 

26 

3.85 

53 • 85 

42.3 

— Acroneuria 

49 

77-4 

6-3 

16.3 

— Perla . . 


8s. 

IS- 







Average for 

80 

= 54 - 

22.3 

23 -7 

Ephemeroidea 





— Ameletus .... 

2 s 


22 . 7 

77-3 

— Baetis sp 

2 


SO. 

50. 

— Drunella 

20 

18.5 

36.8 

44 7 

- — Ephemerella 

28 

3-7 

363 

60 

• — Hept agenia 

34 


24. 

76 




Average for 

109 

= 4-3 

29.7 

66 . 

Trichoptera 





■ — Rhvacophila 

32 

49 

23 - 

28. 

— H vdropsyche 

27 

42. 

54 3 

3-7 

— Brachycentrus 

33 

18.3 

72.7 

9 - 

■ — Thremma 

23 


64. 

36 . 



Average for 

105 

= 28 

54 - 

18. 

Diptera 





— Chironomidae 

6 


71 . 

29. 

— Simulium 

14 


79 

21 




Average for 

20 

= 

76 . 6 

23 4 


“Even from so brief a study as the foregoing certain facts can be gleaned. 
The most notable point is that aquatic insects in rapid streams are opportunists 
as regards food, and eat whatever is available. Secondary to this is the fact 
that the aquatic insects forage extensively, i. e., migrate freely in search of 
food. 

“Both of these points become evident from the collections made in Lost 
Creek, where special efforts were made to select various spots in the creek 
for sample collections of food and of specimens in the vicinity or upon that 
food. Reference to the stomach contents of the individual specimens and com- 
parison with the food items listed for the particular spot shows at once that 
the large majority of specimens contained food that did not occur within main- 
feet of the particular locality. This indicates that these species must be rovers 
and foragers to a marked extent, and that they are opportunists on the whole 
and eat whatever is available. 

“Environmental conditions in mountain streams are strenuous ; the strong 
current in particular makes life somewhat precarious and selective feeding 
difficult. Hence as a result the diet becomes diversified ; the insects take what- 
ever comes along, be it plant, detritus, or animal matter. Their diet thus becomes 


2 3 3 



Fig. 1 1 5. Parnidae larva. Psephenus Iccoutci enlarged xio. 
From Lake Mendota, Wis. 



Fig. 1 1 6. Parnidae larva. Elmis z'ittatiis enlarged xio. From Lake 

Mendota, Wis. 


Ecology of Trout Streams 


233 

much more generalized than the diet of related species in more permissive 
habitats, such as ponds and slow streams. In the latter the less strenuous con- 
dition's permit the insects to select their food, that is. to restrict their diet to 
favored food, and to search for that food. 

“In other words, specialization of habitat leads to diversification of diet 
(i. e., generalization of diet), while generalization of habitat permits a restriction 
of diet, (i. e., specialization of diet).” 

3. The Seasonal Food Cycle. Here. too. I prefer to quote from a prior 
paper (The Food of Trout in Yellowstone Park) : “Besides these main items 
of the normal trout diet in the mountain streams, the so-called ‘water bait,’ 
there is the surface drift or surface bait of water-trapped animals, chiefly insects. 
This comprises especially the weak fliers such as moths, ants and grasshoppers, 
while spiders, centipeds, mice and other animals may occur. But the life of 
a trout stream is dependent on its normal inhabitants, not on the odds and 
ends which a kind wind or accident may provide. It is only during the brief 
summer period that surface bait becomes important ; and for a period of four 
to six weeks the fish are largely dependent on this type of food for their exist- 
ence. That the emergence of their natural water bait, with the resulting depletion 
of this primary food supply, should be synchronous with the summer flights of 
ants, moths, grasshoppers and other poor fliers that are easily water-trapped, 
is one of many instances of the admirable provisions of nature. 

“Indeed, this is carried still further at this period. At this time the minute 
life of the shore waters, especially the shore diatoms, flat- worms, chironomids, 
and the young stages of mayflies, stoneflies and caddisflies, receives a tremend- 
ous impulse and becomes quite prominent. At this period also the young of 
trout, suckers and other fish in the mountain streams can be found in the shore 
pools and shallow rapids feeding on the minute organisms in these places. Here 
lies the remarkable coincidence : the simultaneous appearance and growth of 
fish fry and of a protected food supply for its use. For the older trout are 
unable to get into these shallows, which therefore offer both protection and 
food to the young fish. 

“From the foregoing it is evident that there exist only two well-marked 
periods in the annual cycle of mountain trout streams, namely, a ‘water food’ 
period covering nearly eleven months of the year, and a ‘surface food’ period 
occurring during the summer, and lasting from four to six weeks. This is the 
period when trout, as anglers put it, ‘rise to bait.’ These same periods might 
also be called flood and ebb periods, or flood and drought periods, from the 
fact that high water lasts from October to July, while the ebb or low water 
stage of the summer is really very brief. 

“With the fall rains the brief low water stage ceases and the conditions 
revert to those existing during winter and spring, and continue to the time of 
emergence described, that is, about the first week of July.” 


234 


Roosevelt Wild Life Annals 


COMPARISONS AND SUMMARIES 

Definition of Mountain Stream. Steinmann (’12, p. 125) in his fine paper 
on alpine streams ofifered the following summary : 

1. Conditions and character of mountain streams are: 

a. Constant and low temperature. 

h. Strong current and marked changes in volume of water. 

c. Rich oxygen content. 

d. Paucity of plants. 

e. Stony bottoms. 

2. These characters impress the animal world as follows : 

a. Composed of resistant cosmopolites and stenothermic freshwater forms. 

b. Body shape; morphological adaptations, arrangements for attachment 

holdfasts, dorsoventral flattening, dwarfing, etc. 

c. Life: low food requirements, embryonic development prolonged. 

3. The fauna consists of 

a. Cosmopolites, ubiquists. 

b. Torrenticolar-profound elements. 

c. True stream animals. 

4. The fauna is composed of forms which originally belonged to still water. 

The influence of stream life is recognizable to a different extent in each 
form. 

5. All true mountain stream forms can be regarded as glacial relicts, since they 

agree more or less closely with Zschokke’s postulates in their : 

a. Simultaneous occurrence in mountains in the north. 

b. Simultaneous occurrence in mountains and in lake depths. 

c. Absence from the warm, still and slow moving waters of plains. 

d. Reproduction during low temperature. 

This characterization, while very excellent so far as the fauna is con- 
cerned, is primarily intrinsic, in that it stresses the responses of the animals 
rather than the extrinsic factors which elicit this response. In the present study 
I have attempted to outline what these external factors are. Based on the data 
presented, the following definition of the mountain stream as an ecological unit, 
including both positive and negative characters, is ofifered : 

I. Physiocraphical Characters. 

Positive. N egative. 

1. Constant and considerable change in 

elevation. 

2. Slight depth. 

3. Great and successive changes in types of 

bottoms. 

4. Volume of water relatively small, but im- 

pact very great. 

II. Physiological Characters. 

1. Strong and rapid current, resulting in 1. Uninfluenced by winds. 

2. Equal distribution (= circulation) of; 2. Do not freeze over in winter. 

a. Low and constant temperature. 

b. High oxygen content. 3. No stratification of temperature and oxygen 

c. Substances in solution, affecting the content. Hence no thermocline. 

chemical composition. 

d. Substances in suspension, affecting 

the turbidity or transparency. 


Ecology of Trout Streams 235 

III. Ecological Characters. 

1. Types of habitats. 

a. Permanent, with native biota : white 

water, clear rapids, placid water, 
marginal areas. 

b. Interrupted, with native biota : de- 

posits, splash areas. 

c. Temporary, with transient and tran- 

sitional biota : marginal pools, 

recession areas. 

2 . Distribution of habitats linear or hori- 

zontal, all types intermixed. 

3. Plant life confined to algae and mosses; 

clinging types. 

4. Animal life. 

a. Respiration : all water breathers. 

b. Locomotion : chiefly dingers and 

crawlers. Swimmers move in 
“leaps.” 

c. Structural : usually well protected by 

armor, cases, and webs. 

d. Composition : stoneflies, Blepharo- 

ceridae, Tricladida, are most 
characteristic Invertebrates, trout 
most characteristic Vertebrates. 

e. Food habits generalized, other habits 

specialized. 

Even a superficial examination of these characteristics shows clearly that 
whatever variability exists in different parts of a mountain stream is due to 
physiographical factors; the physiological factors are quite constant. In this 
respect the mountain stream as an ecological unit is outstandingly different 
from other units, since in these the physiological factors are variable, and the 
physiographical ones quite constant. 

Of physiological factors only the current varies, a condition which depends 
entirely on the physiography. All other factors are relatively constant ; thus 
temperature, oxygen content, speed of circulation, chemical makeup, all tend 
to be alike in all parts of a specific mountain stream. 

Another characteristic is that these conditions are distributed horizontally, 
namely, there is no vertical distribution, and hence a lack of the zonation one 
finds in other ecological units. 

Other Aquatic Bodies. As already noted, in this study the factors of 
the environment have been stressed rather than the responses of the organisms 
to these factors, since it is only through the study of these factors that the 
responses can be understood. The following table is an attempt to present in 
comparative form the factors that affect the various aquatic habitats, and the 
chief responses to these factors. The arrangement is based on personal studies 
covering some twenty years. 


— No vertical distribution of habitats into 
zones, as in lakes and slow streams. 

— No emergent vegetation, no higher plants. 


— Surface-breathers absent. 

■ — Free swimmers few. Burrowers are scarce. 


— Soft-bodied forms rare. 

— Plankton organisms absent, Crustacea and 
Annulata rare. No Amphibia. 


Showing in comparative form the factors which affect the various aquatic habitats and the chief responses 

to these factors. 



Roosevelt Wild Life Annals 



Table No. ii. ( Continued ) 


Ecology of Trout Streams 


237 


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238 


Roosevelt Wild Life Annals 


From the table it would be possible to list separately the characteristics of 
each type of aquatic habitat. But since these are already emphasized in the 
table by italics, it would be mere repetition to go through such a procedure. 

In so far as the main work of this study is concerned, it is frankly admitted 
that the results are by no means complete, or even remotely so. The streams 
of the Northwest, in fact, throughout the United States, offer a multitude of 
problems which need prolonged investigation. If the present paper succeeds 
even to a slight extent in stimulating interest and study of some of these prob- 
lems, it will be a recompense for the considerable effort, time, and money spent 
by the writer and other agencies noted in the introduction, in carrying on the 
present study. 

BIBLIOGRAPHY 

An inclusion of all the directly or indirectly relevant literature would 
require the listing of more than a thousand titles. Further, such a list would 
for the larger part be a repetition of what is listed in recent and readily acces- 
sible bibliographies. Hence only directly pertinent literature is cited, together 
with some titles not listed in prior bibliographies. Special attention is called 
to the various papers in Ecology, University of Toronto Studies (publications 
of the Ontario Fisheries Research Laboratory), Illinois Natural History Survey, 
Notes of the Biological Laboratory of the Wisconsin Geological and Natural 
History Survey, Annales de Biologie Lacustre, Archiv fiir Hydrobiologie 
und Planktonkunde, International Revue der gesamten Hydrobiologie und Hydro- 
graphie, Abderhalden’s Handbuch der biologischen Arbeitsmethoden. 

Alexander, Charles 

1925. An Entomological Survey of the Salt Fork of the Vermillion River 
in 1921. with a bibliography of aquatic insects. Bull. 111 . Nat. Hist. 
Surv., 15, pp. 439-535. (Literature prior to 1925 listed.) 
Bornhauser, Konrad 

1912. Die Tierwelt der Quellen in der Umgebung Basels. Int. Rev. d. 

ges. Hydrobiol. u. Hydrogr., Biol. Suppl. 5. pp. 90. (310 titles listed.) 
Brues, Charles T. 

1924. Observations on Animal Life in the Thermal Waters of Yellowstone 
Park, with a consideration of the thermal environment. Proc. 

Am. Acad, of Arts and Sci., 59. pp. 371-487 (good bibliography). 

1924a. Observations on the fauna of Thermal Waters. Proc. Nat. Acad, of 

Sci., 10, pp. 484-486. 

Carpenter, George H. 

1923. Insect Transformation. Pp. 1—280. Dodd, Mead & Co., New \ork. 
Dvxlds, G. S. and Hisaw, F. L. 

1924. Ecological Studies of Aquatic Insects. I. Adaptations of mayfly 

nymphs to swift streams. Ecology, Vol. 5. pp. 137-148. II. Size 
of Respiratory Organs in Relation to Environmental Conditions. 
Ecology, Vol. 5, pp. 262-271. III. Adaptations of caddisfly larvae 
to swift streams. Ecology, Vol. 6, pp. 123-137. 1925. 


Ecology of Trout Streams 


239 


Dyar, Harrison G. and Shannon, Raymond C. 

1927. The North American Two-winged Flies of the Family Simuliidae. 

Proc. U. S. Nat. Mus., Vol. 68, art. 10, pp. 1-54. A monograph. 

Greene, Charles T. 

1926. Description of larvae and pupae of two-winged flies belonging to the 

family Leptidae, Proc. U. S. Nat. Mus., Vol. 70, art. 2, pp. 1-20. 

Hatch, Melville 

1925. An outline of the Ecology of Gyrinidae. Bull. Brooklyn Ent. Soc., 
Vol. 20, pp. 101-114. 

Kennedy, Clarence H. 

1927. Some non-nervous factors that condition the sensitivity of insects to 

moisture, temperature, light and odors. Ann. Ent. Soc. Am., Vol. 
20, pp. 87-106. 

Malloch, John R. 

1917. A preliminary classification of Diptera, exclusive of Pupipara, based 

upon larval and pupal characters with keys to imagines of certain 
families. Bull. 111 . State Lab. Nat. Hist., Vol. 12, pp. 161-409. 
Muttkowski, R. A. 

1918. The Fauna of Lake Mendota: A Qualitative and Quantitative Survey, 

with special reference to the Insects. Trans. Wis. Acad. Sci., 
Vol. 19, pt. 2, pp. 374-482. (Bibl. of aquatics). 

1920. The Respiration of Aquatic Insects: A collective review. Bull. Brook- 

lyn Ent. Soc., Vol. 14, pp. 89-96, 131-141. (Bibliography). 

1925. The Food of Trout in Yellowstone National Park. Roosevelt Wild 

Life Bull., Vol. 2, pp. 470-497. 

Muttkowski, R. A. and Smith, Gilbert M. 

1929. The Food of Trout Stream Insects in Yellowstone National Park. 
Roosevelt Wild Life Annals, Vol. 2, No. 2, pp. 241-263. 

Needham, James G. and others 

1922. A Biological Survey of Lake George, N. Y. State of N. Y. Conserv. 
Comm., pp. 1-78. 

Needham, James G. 

1927. The Rocky Mountain species of the mayfly genus Ephemerella. 

Ann. Ent. Soc. Am., Vol. 20, pp. 107-116. 

Pearse, A. S. 

1926. Animal Ecology. Pp. 1-417. McGraw-Hill Co., New York. 

(Literature listed, but without titles). 

Platt, Ernilie L. 

1916. The Population of the “blanket-algae” of freshwater pools. Am. 
Nat., Vol. 59, pp. 752-762. 

Rousseau, E. 

1921. Les Larves et nymphes aquatiques des Insectes d’Europe. Vol. 1. 

pp. 1-959. 


240 


Roosevelt ll'i/d Life Annals 


Steinmann, Paul 

1907. Die Tierwelt der Gebirgsbache. Eine faunistisch-biologisch Studie. 
Ann. Biol. Lac., II, pp. 1-137. 

Thienemann, A. 

1912. Der Bergbach des Sauerlandes. Int. Rev. d. ges. Hydrobiol. u. 

Hydrogr., Biol. Suppl., 4, pp. 1-125. (Extensive bibliography). 

1926. Der Nahrungskreislauf im Wasser. Verb. d. D. Zool. Ges., Vol. 31. 

Jahresversammlung zu Kiel., pp. 29-79. (Summary of literature 
since about 1918. Bibliography). 

1926a. Hvdrobiologische Untersuchungen an den kalten Quellen und Bachen 
der Halbinsel Jasmund auf Riigen. Arch. f. Hydrobiol. Vol. 17, 
pp. 221-336. 

1926b. Der Bach und der Fluss. in Abderhalden, Handb. d. Biol. Arbeits- 
methoden. Abt. IX, teil 2, lste Halfte, heft 1, pp. 83-96. 

Tillyard, R. J. 

1920. Report on the Neuropteroid Insects of the Hot Springs Regions, X. Z., 
in relation to the problem of trout food. Proc. Linn. Soc. X. S. \\ ., 
Vol. 45. pp. 205-213. 

Ward, Francis 

1920. Animal Life Under Water. Pp. 1-178. Funk and Wagnalls, X T e\v 
York. (Of great interest because of studies by photographic 
methods). 

Yellowstone National Park 

Bull. U. S. Dept. Interior. Publ. annually. With descriptions of forma- 
tions, photographs, maps, list of vertebrate animals, plants and 
bibliography of popular and scientific papers. 


THE FOOD OF TROUT STREAM INSECTS IN YELLOWSTONE 

NATIONAL PARK 

by Richard A. Muttkowski * and Gilbert M. Smith ** 

Collaborators, Field Naturalists, Roosevelt Wild Life Forest Experiment Station, 

Syracuse, New York 

CONTENTS 

PAGE 

Introduction 242 

Description of Localities 243 

The Plants and Animals 244 

General Factors 244 

List of Biota 245 

The Food of the Insects in Trout Streams 246 

Food of the Perloidea or Stoneflies 246 

Food of the Ephemeroida or Mayfly Nymphs 249 

Food of the Trichoptera or Caddisflies 253 

Food of the Diptera 260 

Comparative Summary of the Food of Insects 261 

List of References 262 


* Professor of Biology and Head of the Department of Biology, University of Detroit, Detroit, 
Michigan. 

** Professor of Botany, Stanford University, Palo Alto, California. 


[ 241 ] 


242 


Roosevelt Wild Life Annals 


INTRODUCTION 

The present collaboration is based on certain joint investigations of the authors 
in Yellowstone National Park during the summer of 1921, under the direction 
of the Roosevelt Wild Life Forest Experiment Station, of the New York State 
College of Forestry at Syracuse. During that summer the senior author was 
engaged in the study of the broader problem of the ecology of trout stream 
organisms. In considering the trout stream as an ecological unit, it was necessary 
to study the biota not merely as related to trout, hence as a potential food supply, 
hut also as related to each other. In other words, what is the food supply of the 
various animals inhabiting the trout streams? 

For the study of this phase it was necessary to make a survey of the plant 
life of the streams and the part it plays in the food of the animals. For obvi- 
ously, in the last analysis, all life in trout streams, quite as much as elsewhere, is 
dependent on the plant life. This phase was taken up more intensively after the 
arrival of the junior author in Yellowstone Park in early August, when collec- 
tions were made of the plants of different streams together with associated ani- 
mals. Collections were made from different parts of the streams in order to 
obtain as varied a series of selections as possible in these highly specialized habi- 
tats. For instance, from Lost Creek samples of plant life were obtained from 
the swiftest rapids, from the pools formed by the rapids, from relatively quiet 
waters, from exposed and shaded spots, and also from the lateral pools. 

Specimens were collected jointly from four streams typifying the various 
kinds of trout streams found in Yellowstone Park, — indeed, found throughout 
the Northwest. These are: 1. Yellowstone River, typical of the larger and per- 
manent rapid streams ; 2. Lamar River, a good type of “variable” or fluctuating 
stream, carrying enormous masses of water for short periods, followed by equally 
short periods of rapid recession — on the whole, a stream with a relatively low. 
equable flow; 3. Lost Creek and Tower Creek, both precipitous mountain streams 
of rather short length, with many falls and rapids. Their type is very numerous 
and form the tributaries of the larger streams. Tower Creek is the best repre- 
sentative of this type ; but Lost Creek, a smaller stream, comprises similar con- 
ditions and biota, and was selected because of its convenient location at Camp 
Roosevelt, our field base. 

In each case two comprehensive survey collections were made covering as many 
different habitats as the stream seemed to offer. Besides these, a number of 
isolated collections made previously by the senior author were available for com- 
parison. The collected material was studied while still fresh. This applied 
also to the stomach contents of the various insects. 

In the following pages, the notes on animals are by the senior author, those 
on plants mainly by the junior author. 


Food of Trout Stream Insects 


2 43 


DESCRIPTION OF LOCALITIES 

Yellowstone River, within Yellowstone National Park, has a continuous fall, 
thereby increasing the force of its current enormously. Generally the current 
attains a speed of eight to ten miles per hour, in places up to twenty miles. The 
many rapids, short and long falls and the tortuous bed, make the stream un- 
navigable within the Park. In width it varies from fifty to three hundred feet, 
especially in the “eddies” where the waters are dammed somewhat by the inflow 
of some tributary. The depth may be considerable, some of the “holes” attain- 
ing thirty and even forty feet, and rarely less than six feet, except for a few 
fords. The bed of the stream contains many huge boulders, granite rocks, and 
smaller stones. Hardly anywhere along the Yellowstone does one find sand or 
gravel except in the interstices between the huge boulders and lesser stones along 
parts of shores that are less directly exposed to the current. 

The shores of the Yellowstone are greatly varied, from volcanic rock to allu- 
vial and glacial soil, the latter with the “sulphur slides” so characteristic of the 
canyons of the Yellowstone. In the spring the melting snow carries great quan- 
tities of this soil into the stream which then silts out as the period of high water 
passes. Such slides may, however, occur at any time in the summer and the 
river will then be turbid for a few hours or days, until the loose soil has settled 
or is washed away. 

The Lamar River varies from fifty to one hundred and fifty feet in width, 
and at the ordinary stage is about two feet in depth. Its rapids are of a much 
milder type than those of the Yellowstone, although during the flood period they 
rage with tremendous force and appear formidable. In spring the melting snows 
bring enormous masses of mud and sand with them, which silt out among the 
shore rocks and boulders as the waters recede. — in fact, nearly covering the 
rocks and thus giving little idea of the ferocity of the spring torrents. Yet each 
year, with the spring floods, all these deposits are washed out, to be replaced 
by others coming down from the mountains. 

The bed of the stream is generally clear, composed of granite boulders, and 
rocks usually not smaller than a cubic foot, but of smaller size at the fords. 
The Lamar is essentially a shallow stream and fordable in numerous places. 
Yet it is an excellent stream for trout and supports a rather luxuriant plant 
and animal life. 

The precipitous streams, such as Lost Creek and Tower Creek, because 
of their great vertical fall, have few cobble stones or gravel or sand in their 
beds, except at the margin of the pools. Tower Creek is of practically constant 
width, about twenty to twenty-five feet, for at least seven miles above the falls, 
the junction point with the Yellowstone. The depth varies from eighteen 
inches to two feet. The bed is nearly uniformly composed of rounded cobbles 
varying from pebble size to a cubic foot, with some huge boulders scattered 
along the bed and shores of the stream. 

Lost Creek is ideal for the study of the recession of waters. In flood periods 
(late June) it is an energetic and precipitous torrent which impresses one by the 


244 


Roosevelt Wild Life Annals 


amount and force of the descending waters. A few weeks later, in middle 
August, the creek is a thin trickle carrying a flow of hardly more than a gallon 
per second. Even this disappears entirely into the ground about five hundred 
yards below the pretty Lost Creek Falls in a bed of mixed gravel and cobbles, 
a short distance above Tower Fall Junction Ranger Station. Half a mile down 
the stream reappears as a sump along the Cooke City road, leading down to 
the Cooke City bridge across the Yellowstone River. 

THE PLANTS AND ANIMALS 

General Factors. In such a highly specialized habitat as mountain trout 
streams both physiographical and physiological conditions act restrictively on the 
biota. The constant fall of the water and the resulting tremendous force of the 
current constitute the major factors in limiting the aquatic population. Secure 
places for temporary attachment are few : shelters against the current are none 
too many; there is little opportunity for swimming. Hence only plants and 
animals with holdfasts, — -either natural or artificial, such as webs, claws, suckers 
— or powerful swimmers can establish and maintain themselves. In addition, 
the force of the water makes their resting places rather uncertain, since offal, 
sticks, and stones are constantly being whirled along and strike against the 
rocks. Even larger rocks may he moved by the current ; indeed, well into the 
summer, weeks after the spring floods are over, one can hear the slow' rubbing 
and grinding of the rocks in the stream beds. 

On the other hand, the speed of the water, and the frequent rapids and 
falls make for high oxygen content. Most of the fauna seem to require this. 
If for any reason the oxygen is diminished, or the constant flow ceases, the 
animals die. 

Due to these influences, the fauna is surprisingly sparse in all of the 
streams — that is, in number of species, but not in number of individuals of each 
species. The specialized conditions limit the number of species ; but they also 
tend to increase the numbers of individuals of a species vastly. Hence one finds 
the endemic forms present in astonishing numbers. 

The major portion of the fauna is composed of insects, to exceed 99%, — 
that is, if fish he excluded. One is surprised at the almost complete absence 
of Annelids, leeches, Crustacea, and Mollusca, and at the rarity of Protozoa and 
Rotifera, all of which are so abundant under less violent aquatic conditions. 

The plants are restricted to algae ; all higher plants are absent. Smaller 
algae, diatoms and desmids find shelter in tiny crevices, in the films of emergent 
shore rocks, or behind rocks where the current is not too strong. 

Certain faunistic peculiarities of the streams may be noted. Thus, both 
Tower Creek and Lost Creek are characterized by the abundance of planarians 
and of the caddisworm Hydropsyche, and by the nearly total absence of Simulimn. 
On the other hand, Simulimn is present in quantities in the Yellowstone and the 
Lamar rivers, while planarians are exceedingly rare. The larger Pcrloidca are 
also very characteristic for these two streams. In smaller and precipitous 
streams they seem to be somewhat infrequent. 


food of Trout Stream Insects 245 


List of Biota. 

Alyac and Diatoms. 


Cladophora sp. 

Oscillatoria sp 

Closterinm sp. 

Prasiola sp. 

Cocconeis sp. 

Rlwicospheniutn sp. 

Li pit hernia sp. 

Rhisoclonium sp. 

Gomphonema sp. 

Spirogyra sp. 

M cl 0 sir a sp. 

Synedra sp. 

Nostoc sp. 

( Moss — undetermined ) 

Animals. 


Protozoa 


Ameba sp. 


Col pod a sp. 


Gregarina sp. — as parasites in 

Trichoptera, Perloidea, and Ephemeroidea 

Rotifera 


Several spp. 


Nematoda 


Merrnis (?) sp. — as parasites 

in mayfly nymphs and in Simnlium. 

Arthropoda 


Perloidea. 


Pteronarcys calif ornica 

Doroneuria theodora 

Pteronarcella badia 

Isopcrla 5- punctata 

Acroncuria pacifica 

Perl a verticalis 

Alloperla eoloradensis 

Pcrlodes signata 

Alloperla fidclis 

Pteronarcella badia 

Alloperla lincosa 

Pteronarcys calif ornica 

Alloperla sp. 


Ephemeroidea 


Ameletus sp. 

Ephemerella eoloradensis 

Bactis sp. 

Ephemerella sp. 

Callibaetis sp. 

Hcptagenia sp. 

Drunella grand is 

Iron longimanus 

Trichoptera 


Brachycentrus sp. 

Philopotamus sp. 

Glossosoma sp. 

Platyphylax sp. 

Goera sp. 

Rhyacophila torva 

Hydropsychc sp. 

Thremma sp. 

Limnophilus sp. 

Triaenodes sp. 

Neophylax concinnus 


Diptera 


Ath erix varie ga ta 

Orthocladius sp. 

Bibiocephala comstocki 

Philolutra simplex 

Bibiocephala grandis 

Procladius sp. 

Chamaedipsis sp. 

Psychoda sp. 

Chironomns sp. 

Rhamphoniyia sp. 

Cricotopus varipcs 

Simulium sp. 

Metriocnemus sp. 

Tanytarsus exignus 


246 


Roosevelt Wild Life Annals 


THE FOOD OF THE INSECTS IN TROUT STREAMS 

In the following tables the first numbers are the collection numbers. The 
succeeding number refers to the individual insect whose stomach contents are 
listed. The estimates are given in percentages. “Detritus” signifies unidenti- 
fiable refuse. The figures in parenthesis are the numbers of individual items 
of food. 

The Food of Perloidea or Stoneflies. The table below gives in detail the 
food percentage of the stoneflies as determined from the specimens examined. 

Table No. i. — Showing the Food of the Perloidea or Stoneflies. 


Collec- 

tion 

Num- 

ber 

Number and Name of 
Individual Specimens 

Date 

1921 

Locality 

Habitat 

5517 

1. Pteronarcys californica . . 

July s 

Yellowstone R. 

Rapids near shore. 

5517 

2. Pteronarcys californica. . 

July s 

Yellowstone R. 

Rapids near shore. 

5517 

3. Pteronarcys californica . . 

July 5 

Yellowstone R. 

Rapids near shore. 

5 5 bb J 

3. Acroneuria pacifica 

Aug. 10 

Lost Creek 

Rapids of fair 
violence. 

5S 6 7a 

1. Acroneuria pacifica 

Aug. 1 1 

Yellowstone R. 

Strong rapids 

5567a 

2. Acroneuria pacifica 

Aug. 11 

Yellowstone R. 

Strong rapids .... 

5567a 

3. Acroneuria pacifica 

Aug. 11 

Yellowstone R. 

Strong rapids 

5567a 

4. Acroneuria pacifica 

Aug. 11 

Yellowstone R. 

Strong rapids .... 

5567a 

5. Acroneuria pacifica 

Aug. 11 

Yellowstone R. 

Strong rapids .... 

S567a 

6. Acroneuria pacifica 

Aug. 11 

Yellowstone R. 

Strong rapids .... 

5567a 

7. Acroneuria pacifica 

Aug. 11 

Yellowstone R. 

Strong rapids .... 

SS67a 

8. Acroneuria pacifica 

Aug. 11 

Yellowstone R. 

Strong rapids .... 

5567a 

9. Acroneuria pacifica 

Aug. ti 

Yellowstone R. 

Strong rapids .... 

5567a 

10. Pteronarcys californica . . 

Aug. 11 

Y ellowstone R 

Strong rapids .... 

5567a 

11. Pteronarcys californica . . 

Aug. 11 

Yellowstone R. 

Strong rapids .... 

5567a 

12. Pteronarcys californica . . 

Aug. 11 

Yellowstone R. 

Strong rapids .... 

5572a 

1 . Perla verticalis ? 

Aug. 12 

Lost Creek . . . 

Strong rapids .... 

5574*1 

1. Acroneuria pacifica 

Aug. 13 

Lamar River. . 

Feeding among 

rocks in quiet 
current. 

5574*1 

2. Acroneuria pacifica 

Aug. 13 

Lamar River. . 

Feeding among 

rocks in quiet 
current. 

5574*1 

3. Acroneuria pacifica 

Aug. 13 

Lamar River . 

Feeding among 

rocks in quiet 
current. 

5574*1 

4. Acroneuria pacifica 

Aug. 13 

Lamar River. . 

Feeding among 

rocks in quiet 
current. 

S 5 74*1 

5. Acroneuria pacifica 

Aug. 13 

Lamar River. . 

Feeding among 

rocks in quiet 
current 

5574d 

5575a 

6. Acroneuria pacifica 

1. Acroneuria pacifica 

Aug. 13 
Aug. 14 

Lamar River. . 
Tower Creek. . 

Feeding among 

rocks in quiet 
current. 

Mild rapids 

5575a 

2. Acroneuria pacifica 

Aug. 14 

Tower Creek. . 

Mild rapids 

5575a 

3. Acroneuria pacifica 

Aug. 14 

Tower Creek . . 

Mild rapids 

5575a 

4. Acroneuria pacifica 

Aug. 14 

Tower Creek. . 

Mild rapids 

5575a 

5. Acroneuria pacifica 

Aug. 14 

Tower Creek . 

Mild rapids 

5585a 

20. Acroneuria pacifica 

Aug. 26 

Lost Creek . . . 

In shade. No 

vegetation. 

5585a 

21. Acroneuria pacifica 

Aug. 26 

Lost Creek . . . 

In shade. No 

vegetation. 


Food Items in Percentages 


Intestines with wood fibers, 100. 

Intestines with wood fibers. 1 00. 

Plant matter, 100. 

Heptagenia (2), 75; diatoms, 25. 

Drunella, 25; Heptagenia, 25; 
Rhyacophila, 45; wood frag- 
ments, s. 

Tanytarsus pupa, 100. 

Gregarina. 

Tanytarsus larvae. 99; wood 
fragment, .5; pollen grain of 
pine, .s. 

Tanytarsus (5), 50; Hepta- 
genia, 20; Rhyacophila, 28; 
detritus, 2. 

Tanytarsus (3), so; Ephemerel- 
la, 49; Cladophora, 1. 

Chironomus in tube, 100. 

Empty. 

Detritus, 100. 

Tanytarsus, 100. 

Tanytarsus (3), 5; Cladophora, 
75; shore diatoms, 15; wood 
and bark fragments. 5. 

Small moth, 100. 

Detritus, 100. 

Ephemerella, 40; Heptagenia, 
SO; Chironomus, 9; diatoms, 
I. 

Chironomus larvae, 1 00. 
Gregarina. 

Mayfly fragments. 100. Gre- 
garina. 

Tanytarsus (5), 20; mayfly 
nymph. 50; insect fragments, 
20; detritus, 10. Gregarina. 

Tanytarsus pupae (2), 100. 


Tanytarsus pupae (2), 90; 

wood fragments, 10. Grt- 
garina. 

Bachycentrus (2), 100. 


Heptagenia, 60; Ephemerella, 
20; Perla, 15; detritus, 5. 
Ameletus (4), 100. 

Heptagenia, 60; Rhyacophila 
(a), 40. 

Chironomus pupa, 60; caddis- 
worm, 40. 

Chironomus (2), 40; Pro- 

tenthes, 50; wood fragment, 
10. 

Perla nymphs (5), 35; Chir- 
onomus pupa, 15; Melosira, 
48; wood fragments, 2. 
Insect fragments, is; Melosira, 

8s. 


Food of Trout Stream Insects 


247 


Table No. i. — Showing the Food of the Perloidea or Stoneflies. — 

(Continued) . 


Collec- 

tion 

Num- 

ber 

Number and Name of 
Individual Specimens 

Date 

1921 

Locality 

Habitat 

Food Items in Percentages 

5585a 

22. Acroneuria pacifica | 

Aug. 26 

Lost Creek . . . 

In shade. No 

vegetation. 

Chironomus, 5; Chironomus 
pupa, 20; perla nymphs (12), 
65; Melosira, 5; detritus, 5. 

5585a 

2 3. Acroneuria pacifica 

Aug. 26 

Lost Creek . . . 

In shade. No 

vegetation. 

Insect fragments, 100. 

5585a 

24. Acroneuria pacifica 

Aug. 26 

Lost Creek . . . 

In shade. No 

vegetation. 

Cocconeis, 10; Melosira, 5; dia- 
toms, 5; detritus, 80. 

5585a 

25. Acroneuria pacifica 

Aug. 26 

Lost Creek . . . 

In shade. No 

vegetation. 

Mayfly fragments, 30; Melo- 
sira, 5; detritus, 65. 

5585b 

20. Perla (verticalis) 

Aug. 25 

Lost Creek . . . 

Sunlit parts of 
stream. 

Empty. 

5585b 

21. Perla (verticalis) 

Aug. 25 

Lost Creek . . . 

Sunlit parts of 
stream. 

Heptagenia, 60; Chironomus 
pupa. 25; perla nymphs, 14; 
melosira, 1. 

5585b 

22. Perla (verticalis) 

Aug. 25 

Lost Creek. . . . 

Sunlit parts of 
stream. 

Perla nymphs (7), 99; Melo- 
sira, 1. 

5585 b 

23. Perla (verticalis) 

Aug. 25 

Lost Creek . . . 

Sunlit parts of 
stream. 

Perla nymphs (13), 100. 

5585b 

24. Perla (verticalis) 

Aug. 25 

Lost Creek . . . 

Sunlit parts of 
stream. 

Chironomus pupa, 30; Melo- 
sira, 50; said, 10; wood 
fragments, 10; all in clearly 
marked zones in stomach. 

5589a 

12. Pteronarcys californi a.. 

Aug. 26 

Lamar River. . 

Strong rapids 

among moss and 
Cladophora. 

Moss, 60, bark, 35; diatoms, 5. 

5589a 

13. Pteronarcys californi. a. . 

Aug. 26 

Lamar River . . 

Strong rapids 

among moss and 
Cladophora. 

Moss, 80; Epithemia, 20. 

5589a 

14. Pteronarcys californi a.. 

Aug. 26 

Lamar River. . 

Strong rapids 

among moss and 
Cladophora. 

Moss, 50; diatoms, 10; Epi- 
themia, 40. 

5589a 

15. Pteronarcys californica . . 

Aug. 26 

Lamar River. . 

Strong rapids 

among moss and 
Cladophora. 

Moss, 85; diatoms, i; Epi- 
themia, 14. 

5589a 

16. Pteronarcys californica. . 

Aug. 26 

Lamar River.. 

Strong rapids 

among moss and 
Cladophora. 

Moss, 50; diatoms, 10; Epi- 
themia, 40. 

5589a 

17. Pteronarcys californica. . 

Aug. 26 

Lamar River. . 

Strong rapids 

among moss and 
Cladophora. 

Epithemia, 100. Small amount. 

5589a 

1 Acroneuria pacifica 

Aug. 26 

Lamar River. . 

Strong rapids 

among moss and 
Cladophora. 

Ephemerella nymph, 99; moss, 

1. 

5589a 

19. Acroneuria pacifica 

Aug. 26 

Lamar River . . 

Strong rapids 

among moss and 
Cladophora. 

Insect fragments, 100. 

5589b 

8. Acroneuria pacifica 

Aug. 26 

Lamar River . . 

Minor rapids, 

among decaying 
Cladophora. 

Chironomus larvae (16), 40; 
Perla, 40; sand, 20. 

5589b 

9. Acroneuria pacifica 

Aug. 26 

Lamar River. . 

Minor rapids, 

among decaying 
Cladophora. 

Chironomus larvae (19), 95; 
sand, 5. 

5589b 

10. Acroneuria pacifica 

Aug. 26 

Lamar River. . 

Minor rapids, 

among decaying 
Cladophora. 

Chironomus larvae (16), 90; 
Epithemia, 5; diatoms, 5. 

5589b 

1 1. Acroneuria pacifica 

Aug. 26 

Lamar River. . 

Minor rapids, 

among decaying 
Cladophora. 

Chironomus larvae (6), 40; 
Perla nymphs, 50; insect 
fragments, 10. 

5589b 

12. Acroneuria pacifica 

Aug. 26 

Lamar River. . 

Minor rapids, 

among decaying 
Cladophora. 

Perla numphs, 45; mayfly 
nymph fragments, 50; sand, 

S- 

5589b 

13. Acroneuria pacifica 

Aug. 26 

Lamar River. . 

Minor rapids, 

among decaying 
Cladophora. 

Chironomus larvae (2), 100. 

559 oa 

1. Acroneuria pacifica 

Aug. 26 

Yellowstone R. 

Moderate rapids 

Chironomus larvae (4), 40; 
Rhyacophila, 50; sand, 10. 
Gregarina. 

5 5 90 a 

2. Acroneuria pacifica 

Aug. 26 

Yellowstone R. 

Moderate rapids. . 

Insect fragments, ioo. Ore- 

5500a 

3. Acroneuria pacifica 

Aug. 26 

Yellowstone R. 

Moderate rapids. . 

Rhyacophila, ioo. 

5590 a 

4. Pteronarcys californica . . 

Aug. 26 

Yellowstone R. 

Moderate rapids.. 

Detritus, 100. 

5590 a 

5. Pteronarcys californica. . 

Aug. 26 

Yellowstone R. 

Moderate rapids.. 

Detritus, ioo. 

5590 a 

6. Pteronarcys californica . . 

Aug. 26 

Yellowstone R. 

Moderate rapids. . 

Detritus, 100. 

5590 a 

7. Pteronarcys californica. . 

Aug. 26 

Yellowstone R. 

Moderate rapids. . 

Detritus, ioo. 

5590 a 

8. Pteronarcys californica. . 

Aug. 26 

Yellowstone R. 

Moderate rapids.. 

Trebonema, 5; moss fragments, 
10; detritus, 85. 

55903 

9. Pteronarcys californica . . 

Aug. 26 

Yellowstone R. 

Moderate rapids.. 

Trebonema, 15; moss frag- 
ments, 5; diatoms, 10; 
detritus, 70. 


2 4 8 


Roosevelt Wild Life Annals 


Table No. i. — Showing the Food of the Perloidea or Stoneflies. — 

( Concluded ). 


Collec- 

tion 

Num- 

ber 

Number and Name of 
Individual Specimens 

Date 

1921 

Locality 

Habitat 

Food Items in Percentages 

559oa 

10. Pteronarcys californica. . 

Aug. 

26 

Yellowstone R. 

Moderate rapids. . 

Bark fragments, 85; detritus. 

5590a 

11. Pteronarcys californica. . 

Aug. 

26 

Yellowstone R. 

Moderate rapids.. 

*5- 

Trebonema, 3; detritus, 97. 

5590b 

1 . Pteronarcys californica . . 

Aug. 

26 

Yellowstone R. 

Moderate rapids. . 

Wood fragments, 85; detritus. 

5590b 

2. Pteronarcys californica. . 

Aug. 

26 

Yellowstone R. 

Moderate rapids. 

!5- 

Detritus, ioo. 

5590b 

3. Pteronarcys californica . . 

Aug. 

26 

Yellowstone R. 

Moderate rapids. . 

Sand, s; diatoms, 5; detritus. 

5 5 90b 

4. Pteronarcys californica. . 

Aug. 

26 

Yellowstone R. 

Moderate rapids.. 

90. 

Wood fragments, 40; diatoms, 
10; Trebonema, 5; detritus, 

5 59ob 

5. Pteronarcys californica. . 

Aug. 

26 

Yellowstone R. 

Moderate rapids. . 

45* 

Wood fragments, 3; diatoms, 5; 
Trebonema, 2; detritus, 90. 

5590b 

6. Acroneuria pacifica 

Aug. 

26 

Yellowstone R. 

Moderate rapids. . 

Insect fragments, 95; diatoms. 

559ob 

7. Acroneuria pacifica 

Aug. 

26 

Yellowstone R. 

Moderate rapids.. 

5- 

Rhyacophila pupa (2), 100. 

5590b 

8. Acroneuria pacifica 

Aug. 

26 

Yellowstone R. 

Moderate rapids.. 

Chironomus (2), 90; sand. 10. 

5590b 

9. Acroneuria pacifica 

Aug. 

26 

Yellowstone R. 

Moderate rapids.. 

Empty. 

5590C 

1. Pteronarcys californica. . 

Aug. 

26 

Yellowstone R. 

Strong, violent 

rapids. 

Bark, 95; detritus. 5. 

5590C 

2. Pteronarcys californica . . 

Aug. 

26 

Yellowstone R. 

Strong, violent 

rapids. 

Bark, 25; detritus, 75. 

5590C 

3. Pteronarcys californica. . 

Aug. 

26 

Yellowstone R. 

Strong, violent 

rapids. 

Bark, 50; detritus, 50. 

5590C 

4. Pteronarcys californica . . 

Aug. 

26 

Yellowstone R. 

Strong, violent 

rapids. 

Empty. 

559ia 

7. Acroneuria pacifica 

Aug. 

27 

Tower Creek. . 

Minor rapids 

Mavfly fragments, ioo. 

559ia 

8. Acroneuria pacifica 

Aug. 

27 

Tower Creek. . 

Minor rapids 

Detritus, 100. 

559la 

9. Acroneuria pacifica 

Aug. 

27 

Tower Creek. . 

Minor rapids 

Empty. 

5591a 

10. Acroneuria pacifica 

Aug. 

27 

Tower Creek. . 

Minor rapids 

Detritus, 100. 

559ia 

1 1 . Acroneuria pacifica 

Aug. 

27 

Tower Creek. . 

Minor rapids 

Mayfly fragments, 95; detritus. 

559ia 

12. Acroneuria pacifica 

Aug. 

27 

Tower Creek. . 

Minor rapids 

5* 

Moth scales, 50; detritus. 50. 

5591a 

13. Acroneuria pacifica 

Aug. 

27 

Tower Creek. . 

Minor rapids 

Chironomus larvae, 90; detri- 
tus, 10. 

559lb 

6. Acroneuria pacifica 

Aug. 

27 

Tower Creek. . 

Strong rapids .... 

Digested matter, ioo. 

559lb 

7. Acroneuria pacifica 

Aug. 

27 

Tower Creek. . 

Strong rapids .... 

Detritus, 100. 

S59lb 

8. Alloperla sp 

Aug. 

27 

Tower Creek. . 

Strong rapids .... 

Digested matter (plants?), 100. 


Table No. 2. — Showing Summary of Food of Perloidea. (Empty Stomachs 
are not Included in Computing the Averages). 


Name 

Locality 

Number 

of 

Specimens 

Animal 

Food 

Plant 

Food 

Detritus 

Pteronarcys 

Yellowstone River 

20 

s 

43 

90 

53 85 

I 

52 

10 

Pteronarcys 

Lamar River 

6 


Average for 

Acroneuria 

Yellowstone River 

26 = 

14 

14 

3.85 

90 

95 5 

50 

60 

42.3 

9 

Acroneuria 

Acroneuria 

Lamar River 

Lost Creek 

1 . 5 
30 
5 

63 

15 

3 

20 

Acroneuria 

Tower Creek 

11 

3 S 

Average for 

Perl a verticalis (?). . . 


= 77-4 

85 

16.3 






Food of Trout Stream Insects 


249 


Undoubtedly, the stoneflies are the dominant insect forms of the mountain 
trout streams, particularly in Yellowstone and Lamar rivers. Previous to their 
final eedysis, about the time the spring floods abate, the nymphs are extremely 
abundant and appear to constitute the hulk of the insect fauna. The stomachs 
of trout taken from the stream at this period are largely filled with stonefly 
nymphs. 

But where are all these nymphs to obtain their food? They are carni- 
vores, one generally reads. But if their numbers are so great that their hulk 
exceeds the available animal food supply, how can they subsist? This was 
one of the puzzles the senior author met early in the work, — one which was 
not solved until the present data were obtained. 

From the examination of the stomach contents of Perlid nymphs several 
surprising results were obtained : ( I ) That Perloidea are not exclusively 

carnivores, but that their diet contains an admixture of plant matter and 
detritus, i. e., predigested and decomposed matter. (2) That the largest species, 
Ptcronarcys calif ornica, is largely a vegetarian. (3) That about 12% of those 
Perloidea whose main diet was animal matter, were parasitized by gregarines. 

The diet of Ptcronarcys was perhaps the most surprising result. It’s first 
notice was so unexpected that thereafter special efforts were made to secure a 
considerable number of specimens from different localities for examination. 
W hether this species is really a vegetarian, or whether it is so only on occasion, 
.cannot be stated positively. Only this much seems clear: The specimens 

examined, about thirty in number, had fed chiefly on a plant diet, averaging 
less than 4% animal diet. 

The other prominent perlid species, Acroneuria pacifica, is quite evidently 
a carnivore. The admixture of plant food and detritus may be accounted for 
on the basis that they were taken in with the insect food. It is also possible, 
that the gregarines found in six of the Acroneuria were not “resident” parasites, 
but were taken in with some insect hosts, such as mayfly nymphs or caddisworms. 

In a very interesting study of Nemoura, C. F. Wu (’23, p. 39) remarks 
as follows: “Besides some fine sediment and the half digested fragments of 

decaying leaves, there were found great varieties of unicellular algae, chiefly 
diatoms and desmids. No remains of animal tissue have ever been detected, 
so that naiads are herbivorous in their food habits.” Relative to the food of 
the adult Wu ( 1 . c.) states, “Of the various kinds of living plant leaves found 
around the water and fed to the adults, the young leaves of Touch-me-not are 
eaten.” Newcomer (T8) reports the adults of Taeniopteryx pacifica as feeding- 
on the buds and leaves of plants and causing considerable injury. 

Food of Ephemeroidea or Mayfly Nymphs. The following table shows 
in detail the food percentages of the mayfly nymphs examined. 


250 


Roosevelt Wild Life Annals 

Table No. 3. — Showing Food of Mayfly Nymphs. 


Collec- 

tion 

Num- 

ber 

Number and Name of 
Individual Specimens 

Date, 

1921 

Locality 

55Mb 

3. Ameletus 

Aug. 10 

Lost Creek .... 

5566b 

I. Drunella sp 

Aug. 10 

Lost Creek .... 





5566d 

1. Drunella sp 

Aug. 10 

Lost Creek .... 

5566d 

2. Drunella sp 

Aug. 10 

Lost Creek .... 

5Sb6d 

5. Ephemerella sp. . . 

Aug. 10 

Lost Creek 

5566(1 

6. Ephemerella sp. . . 

Aug. 10 

Lost Creek .... 

5S66j 

I. Heptagenia sp . . . . 

Aug. 10 

Lost Creek .... 

SS f >6h 

4. Ephemerella sp. . . 

Aug. 10 

Lost Creek .... 

55 b 6 i 

i . Ephemerella sp . . . 

Aug. 10 

Lost Creek .... 

5566i 

2. Ephemerella sp. . . 

Aug. 10 

Lost Creek .... 

5566 j 

2. Heptagenia sp . . . 

Aug. 10 

Lost Creek .... 

5566) 

7. Ephemerella sp. . 

Aug. 10 

Lost Creek .... 

ssftftj 

8. Ephemerella sp. . 

Aug. 10 

Lost Creek .... 

5566k 

1. Heptagenia sp . . 

Aug. 10 

Lost Creek .... 

5566 k 

2. Ameletus sp 

Aug. 10 

Lost Creek .... 

55661 

1 . Ephemerella sp . . . 

Aug. 10 

Lost Creek .... 

55661 

2. Ephemerella sp. . 

Aug. 10 

Lost Creek .... 

5567a 

IS- Ameletus sp 

Aug. 11 

Yellowstone R 

S567a 

16-19. Ameletus sp. . . 

Aug. 11 

Yellow'stone R 

5567a 

20. Ameletus sp 

Aug. 1 1 

Yellowstone R 

5567a 

21, 22. Ameletus sp . . 

Aug. 1 1 

Yellowstone R 

5567a 

23. Heptagenia sp 

Aug. 11 

Yellowstone R . 

5567a 

24. Heptagenia sp . . . 

Aug. 11 

Yellowstone R . 

5567a 

25. Heptagenia sp. 

Aug. 11 

Yellow'stone R . 

5567a 

26. Heptagenia sp . . . 

Aug. 11 

Yellowstone R . 

5567a 

27. Heptagenia sp. . . . 

Aug. 11 

Yellowstone R 

5567a 

28. Heptagenia sp . . . 

Aug. 11 

Yellowstone R . 

5567a 

29. Ephemerella sp . . 

Aug. 11 

Yellowstone R. 

5567a 

30. 51. Ephemerella sp. 

Aug. 11 

Yellowstone R . 

5567a 

32. Ephemerella sp. . . 

Aug. 11 

Yellowstone R . 

5567a 

33, 34. Ephemerella sp. 

Aug. 11 

Yellow'stone R 

5572a 

4. Ameletus sp 

Aug. 12 

Lost Creek .... 

5572a 

5, 6. Ameletus sp . . 

Aug. 12 

Lost Creek .... 

5572a 

7. Heptagenia sp . . 

Aug. 12 

Lost Creek .... 

5572b 

5. Ameletus sp 

Aug. 12 

Lost Creek .... 

5 572b 

6. Ameletus sp 

Aug. 12 

Lost Creek .... 

5572b 

7. Ameletus sp 

Aug. 12 

Lost Creek .... 

5572b 

8. Ephemerella sp 

Aug. 12 

Lost Creek .... 

5572b 

Q. Ephemerella sp . . 

Aug. 12 

Lost Creek .... 


Habitat 


From rocks with clusters of 
vegetation, chiefly Melo- 
sira and some Gompho- 
nema and Closterium. 

Pure Melosira 


From Prasiola and Oscil- 
latoria. 

From Prasiola and Oscil- 
latoria. 

From Prasiola and Oscil- 
latoria. 

From Prasiola and Oscil- 
latoria. 

From Prasiola 

From barren region 

Barren region w'ith few 
diatom snells. 

Barren region with few 
diatom shells. 

Barren, with few' diatoms. 

Barren, w'ith few diatoms. 
Barren, with few diatoms. 

Barren with few' diatoms, 
some Closterium. 

Barren w'ith few' diatoms, 
some Closterium. 

Mostly Oscillatoria. 

Traces of Melosira. 
Mostly Oscillatoria. 

Traces of Melosira. 

Strong rapids 

Strong rapids 

Strong rapids 

Strong rapids 

Strong rapids 

Strong rapids 

Strong rapids 

Strong rapids 

Strong rapids 

Strong rapids 

Strong rapids 

Stroi g rapids 

Strong rapids 

Strong rapids 

Rapids. Vegetation: Melo- 
sira, Prasiola, Oscilla- 
toria, Calpoda and Roti- 
fera among plants. 
Rapids. Vegetation: Melo- 
sira, Prasiola, Oscilla- 
toria, Calpoda and Roti- 
fera among plants. 
Rapids. Vegetation: Melo- 
sira, Prasiola, Oscilla- 
toria, Calpoda and Roti- 
fera among plants. 
Among rocks in rapids. 
Much detritus and 

Melosira. 

Among rocks in rapids. 
Much detritus and 

Melosira. 

Among rocks in rapids. 
Much detritus and 

Melosira. 

Among rocks in rapids. 
Much detritus and 

Melosira. 

Among rocks in rapids. 
Much detritus and 

Melosira. 


Food Items in Percentages 


Melosira, 90; Gompnonema, 
10. 


Melosira, 99; Gomphonema, 
•5; protozoan. .5. 

Melosira, 99; Gomphonema, 

1. 

Melosira, 80; Closterium, 1; 
Oscillatoria, 19. 

Prasiola, 99; Oscillatoria, 1. 

Melosira, 50; empty diatom 
shells, 50. 

Prasiola, 100. 

Melosira. 60; Oscillatoria, 40. 

Empty. 

Melosira, 75; mixed diatoms, 
2 5* 

Melosira, 95; mixed diatoms, 
5. 

Melosira, 50; Oscillatoria, 
45; diatoms. 5. 

Prasiola, 99; Oscillatoria. 1. 

Gomphonema, 85; diatoms, 
I 5- 

Melosira, 85; diatoms ard 
Closterium, 15. 

Melosira, 100. 

Oscillatoria, 99; diatoms, 1. 

Oscillatoria, 99; diatoms, 1. 

Sand, 95; diatoms, 5. 

Detritus, 100. 

Fresh diatoms, 15; sana, 85. 

Botn witn detritus, 100. 

Detritus, 100. 

Sand, 50; diatoms, 5; detri- 
tus, 45. 

Detritus, 100. 

Sand. 15; diatoms, 5; detri- 
tus, 80. 

Sand, 5; diatoms, 5; detri- 
tus, 90. 

Diatoms, 5; detritus, 95. 

Cladophora. 5; sand, 10; 
detritus, 85. 

Botn with detritus, 100. 

Detritus, 75; adult dipteran, 

25. 

Both with detritus, 100. 

Melosira, 50; detritus. 50. 


Both with detritus, 100. 


Rock diatoms, 15; sand, 5; 
detritus, 80. 


Melosira, 50; detritus, 50. 


Detritus, 50; sand, 25; rock 
diatoms, 25. 

Rock diatoms, 75*. detritus, 
20; sand, 5. 

Rock diatoms, 85; detritus, 
5; diatoms, 10. 

Rock diatoms, 75; detritus. 
23; sand. 2. 


Food of Trout Stream Insects 


251 


Table No. 3. — Showing Food of Mayfly Nymphs. — (Continued) . 


Collec- 

tion 

Num- 

ber 

Number and Name of 
Individual Specimens 

Date, 

1921 

Locality 

Habitat 

Food Items in Percentages 

5572b 

10. Drunella sp 

Aug. 12 

Lost Creek .... 

Among rocks in rapids. 
Much detritus and 

Melosira. 

Wood fibers, 35; detritus, 65. 

5572e 

1. Heptagenia sp 

Aug. 12 

Lost Creek ... 

From rocks in rapids. 
Moss and Prasiola. 
Melosira caught in moss. 

Detritus, 95; wood frag- 
ments, 2; mixed diatoms, 
3- 

557 2 e 

2, 3. 4. Heptagen a 
sp. 

Aug. 12 

Lost Cee'c 

From rocks in rapids. 
Moss and Prasiola. 
Melosira caught in moss. 

All with de r.tus, ioo. 

557 2 e 

5. Heptagenia sp. . . . 

Aug. 12 

Lost Creek .... 

From rocks in rapids. 
Moss and Prasiola. 
Melosira caught in moss. 

Detritus, 95; mixed diatoms, 
5. 


i. Baetis sp 

Aug. 14 

Tower Creek . 

Mild rapids 

Sand, 20; detritus, 80. 
Detritus, ioo. 


2. Baetis sp 

Aug. 14 

Tower Creek . 

Mild rapids 

5575c 

1 . Ephemerella sp . . . 

Aug. 14 

Tower Creek . . . 

From lateral rapids 

Sand, 20; detritus, 80. 

5575c 

2. Ephemerella sp. . . 

Aug. 14 

Tower Creek . . . 

From lateral rapids 

Sand, 10; detritus, 50; wood 
fragments, 15; insect frag- 
ments, 25. 

5575c 

5575d 

3, 4. Ephemerella sp. 

Aug. 14 

Tower Creek 

From lateral rapids 

Detritus, ioo. 

i . Ameletus sp 

Aug. 14 

Tower Creek . . . 

Mild rapids 

Diatoms, 1 ; wood fragments, 
4; detritus, 75; sand, 20. 

5575e 

1. Ephemerella sp. . . 

Aug. 14 

Tower Creek . . . 

From lesser rapids 

Heptagenia, 50; detritus, 49; 
wood, 1. 

5584a 

15. Heptagenia sp. . . . 

Aug. 25 

Lost Creek .... 

Shaded area. Xo vegeta- 
tion. 

Detritus. 30; Cocconeis. 65; 
wood fragments, 2; mixed 
fragments, 3. 

5584a 

16. Heptagenia sp 

Aug. 25 

Lost Creek .... 

Shaded area. Xo vegeta- 
tion. 

Cocconeis, 25; Rhoicos- 
phenia, 25; mixed diatoms, 
5; detritus, 40; sand, 5. 

5584a 

17. Drunella sp 

Aug. 25 

Lost Creek .... 

Shaded areas. No vegeta- 
tion. 

Cocconeis, 40; Rhoicos- 
phenia, 5; mixed diatoms, 
5; detritus. 50. 

5584a 

18. Drunella sp 

Aug. 25 

Lost Creek .... 

Shaded areas. Xo vegeta- 
tion. 

Cocconeis, 35; Melosira, 15; 
Synedra, 3; mixed dia- 
toms, 7; sand. 5; detritus. 

5584a 

19. Drunella sp 

Aug. 25 

Lost Creek .... 

Shaded areas. X'o vegeta- 
tion. 

35- 

Sand, 25; Cocconeis, 25; 
Melosira, 5; mixed dia- 
toms, 5; detritus, 40. 

5589a 

20. Drunella sp 

Aug. 26 

Lamar River . . . 

Strong rapids. Feeding on 
moss and Cladophora. 

Epithemia, 80; Cocconeis,. 

10; mixed diatoms, 10. 
Epithemia, 50; detritus, 50. 

5589a 

21. Drunella sp 

Aug. 26 

Lamar River . . . 

Strong rapids. Feeding on 
moss and Cladophora. 

5589b 

14. Ephemerella sp . . 

Aug. 26 

Lamar River . . 

Minor rapids. Feeding 

among decaying Clado- 
phora. 

Chironomus (2), 5; Epi- 

themia, 50; mixed diatoms, 
10; detritus, 35. 

Sand, 5; Epithemia, 50; 
mixed diatoms, 10; detri- 
tus, 35- 

5589b 

15. Ephemerella sp . . . 

Aug. 26 

Lamar River . . 

Minor rapids. Feeding 

among decaying Clado- 
phora. 

5589b 

16. Ephemerella sp . . 

Aug. 26 

Lamar River. . . 

Minor rapids. Feeding 

among decaying Clado- 
phora. 

Sand, 5; Epithemia, 15; dia- 
toms, 10; detritus, 70. 

5589b 

17. Ephemerella sp. . . 

Aug. 26 

Lamar River. . . 

Minor rap ds. Feeding 

among decaying Clado- 
phora. 

M:x d d atoms, 5; detritus,. 
95- 

5589b 

18. Ameletus sp 

Aug. 26 

Lamar River . . . 

Minor rapids. Feeding 

among decaying Clado- 
phora. 

Epithemia, 75; diatoms, 10; 
detritus, 15. 

5589b 

19, 20. Ameletus sp. . 

Aug. 26 

Lamar River . . . 

Minor rapids. Feeding 

among decaying Clado- 
phora. 

Both with Epithemia, 10; 
diatoms, 15; detritus, 75.. 

5590a 

13. Heptagenia sp. .. . 

Aug. 26 

Yellowstone R . 

Moderate rapids 

Cladophora, 90; sand, 10. 

5590a 

14. Heptagenia sp . . . 

Aug. 26 

Yellowstone R . 

Moderate rapids 

Detritus, 100. 

5590b 

9. Ephemerella sp . . . 

Aug. 26 

Y ellowstone R . 

Minor rapids 

Detritus, ioo. 

5590b 

10. Ephemerella sp. . . 

Aug. 26 

Yellowstone R . 

Minor rapids 

Detritus, 85; diatoms, 5; 
Trebonema, 10. 

5590b 

11. Ephemerella sp. . . 

Aug. 26 

Yellowstone R . 

Minor rapids 

Detritus, 90; diatoms, 5; 
Trebonema, 5. 

559ia 

14. Heptagenia sp . . . . 

Aug. 27 

Tower Creek . . 

Minor rapids 

Detritus, 100. 

559ia 

15. Heptagenia sp. . . . 

Aug. 27 

Tower Creek . . . 

Minor rapids 

Detritus, 99; diatoms, 1. 

559ia 

16. 17, 18. Heptagenia 

Aug. 27 

Tower Creek . . . 

Minor rapids 

All with detritus, ioo. 

559ia 

sp. 

19. Ameletus sp 

Aug. 27 

Tower Creek . . 

Minor rapids 

Sand, 15; detritus, 85. 

559ia 

20. Ameletus sp 

Aug. 27 

Tower Creek . . . 

Minor rapids 

Sand, 18; detritus, 80; dia- 
toms, 2. 

559ia 

21. Ephemerella sp. . . 

Aug. 27 

Tower Creek . . . 

Minor rapids 

Sand, 1; detritus, 97; dia- 
toms, 2. 

559ia 

22. Ephemerella sp . . . 

Aug. 27 

Tower Creek. . . 

Minor rapids 

Sand, 1; detritus, 97; dia- 
toms, 2. 

559ia 

23. Drunella sp 

Aug. 27 

Tower Creek . . . 

Minor rapids 

Insect fragments, 50; wood 
fragments, 45; detritus, 5.. 
Gregarina as parasites. 


252 Roosevelt Wild Life Annals 

Table No. 3. — Showing Food of Mayfly Nymphs. — (Concluded) . 


Collec- 

tion 

Num- 

ber 

Number and Name 0* 
Individual Specimens 

Date, 

1921 

Locality 

Habitat 

Food Items in Percentages 

5591a 

5591a 

24. Drunella sp 

25. Drunella sp 

Aug. 27 
Aug. 27 

Tower Creek . . . 
Tower Creek . . . 

Minor rapids 

Minor rapids 

Wood fragments, 10; detri- 
tus. 90. Gregarina. 
Insect fragments. 80; dia- 
toms, 2; detritus, 18. 
Gregarina. 

5591a 

5591a 

26. Drunella sp 

27. Drunella sp 

Aug. 27 
Aug. 27 

Tower Creek . . . 
Tower Creek . . . 

Minor rapids 

Minor rapids 

Detritus, 100. Gregarina. 
Insect fragments, 5; wood 
fragments, 10; sand, 4; 
diatoms, 1 ; detritus, 80. 

5591a 

28. Heptagenia sp . . 

Aug. 27 

Tower Creek . . . 

Minor rapids 

Diatoms, 20; detritus, 70; 
sand, 10. With nematode 
(Mermis sp.?) as parasite. 

5 S 9 ia 

29. Heptagenia sp . . 

Aug. 27 

Tower Creek. . . 

Minor rapids 

Diatoms. 20; detritus, 70; 
sand, 10. With two nema- 
tode parasites (Mermis 
sp.?). 

Detritus, 100. 

559 ib 

9 - Ameletus sp 

Aug. 27 

Tower Creek. . 

Strong rapids 

559 ib 

10. Ameletus sp 

Aug. 27 

Tower Creek . 

Strong rapids 

Detritus, 95; diatoms, 5. 

559 ib 

1 1 . Ameletus sp 

Aug. 27 

Tower Creek . 

Strong rapids 

Detritus, 94; sand, 5; dia- 
toms. 1. 

5591 b 

12. Drunella sp 

Aug. 27 

'Power Creek . . 

Strong rapids 

Insect fragments, 75; sand. 
5; detritus, 20. With 

gregarina. 

559 lb 

559 lb 

13. Drunella sp 

14. Drunella sp 

Aug. 27 
Aug. 27 

Tower Creek . . . 
Tower Creek . . 

Strong rapids 

Strong rapids 

Insect fragments. 10; sand, 
5; detritus. 85. Gregarina. 
Bark fragments. 20; sand, 5; 
detritus, 75- Gregarina. 

559 lb 

15. Drunella sp 

Aug. 27 

Tower Creek . . . 

Strong rapids 

Diatoms, 2; sand, 23; detri- 
tus, 75 - Gregarina. 

559 lb 

16. Heptagenia sp. . . 

Aug. 27 

Tower Creek 

Strong rapids 

Detritus. 100. 

559 lb 

17. Heptagenia sp . 

Aug. 27 

T ower Creek . . 

Strong rapids 

Diatoms, 5; sand, 5; detritus. 

559 lb 

18. Heptagenia sp. . 

Aug. 27 

Tower Creek. . 

Strong rapids 

90. 

Sand. 5; detritus, 95 - 

559 ie 

2. Heptagenia sp . . . . 

Aug. 27 

Tower Creek. . . 

Lateral pools. With mod- 
erate current. 

Detritus, ioo. 

55919 

3, 4. Heptagenia sp. 

Aug. 27 

Tower Creek. . . 

Lateral pools. With mod- 
erate current. 

Both with detritus, 100. 

559 ie 

5. Drunella sp 

Aug. 27 

Tower Creek . . . 

Lateral pools. With mod- 
erate current. 

Insect fragments, 100. Gre- 
garina. 

559 ie 

6 . Drunella sp 

Aug. 27 

Tower Creek . . 

Lateral pools. With mod- 
erate current. 

Insect fragments, 50; wood 
fragments, 20; detritus, 
30. Gregarina. 


Food of Trout Stream Insects 

Table No. 4. — Showing Summary of Food of Mayfly Nymphs. 


253 


Name 


Locality 


Number 

of 

Specimens 


Animal 

Food 


Plant 

Food 


Detritus 


Yellowstone R. 
Lamar River . . 
Lost Creek. . . 
Tower Creek. . 


Ameletus sp 

Ameletus sp 

Ameletus sp 

Ameletus sp 

Average for . . 

Drunella sp 

Drunella sp 

Drunella sp 

Average for 

Baetis sp Tower Creek 


Lamar River. 
Lost Creek. . 
Tower Creek. 


Ephemerella sp . . . . 

Ephemerella sp 

Ephemerella sp 

Ephemerella sp . . . . 
Average for 

Heptagenia sp 

Heptagenia sp 

Heptagenia sp 

Average for .... 


Yellowstone R . 
Lamar River . . 
Lost Creek . . . . 
Tower Creek. . 


Yellowstone R . 
Lost Creek. . . 
Tower Creek. . 


8 

3 

8 

6 

25 

2 

7 

11 

20 


9 

4 

8 

7 
28 

8 
13 

13 

34 


33-6 

18.5 


2.6 

125 


11 

3-7 


2 

45 

50 

3 

22 . 7 

75 

68 

10 

36.8 
50 

3-4 

37 

96.25 

10 

36.3 

14 

50 

4 

24 


98 

55 

50 

97 

77 -3 

25 

32 

56.4 

44-7 

50 

94 

6i.75 

3-75 

79 

60 

86 

50 

96 

76 


From the predominance of detritus in the food of mayfly nymphs, as 
indicated by the averages, it would seem that these nymphs are primarily 
scavengers. They appear to feed on the flotsam and jetsam that is caught 
between rocks, on diatoms, and the bits of filamentous algae that grow on 
rocks. The animal matter eaten may possibly be dead specimens caught with 
the flotsam. 

Of Drunella ten specimens, and these all from Tower Creek, were parasit- 
ized by gregarines. Two Heptagenia are noted as parasitized by a nematode, 
perhaps a species of Mermis; these, too, were taken from Tower Creek. In 
another paper (Muttkowski, ’25, Fig. 124, facing p. 485) is shown an adult 
mayfly with such a nematode emerging from the caudal end. This adult was 
taken from Gardiner River, at its junction with Lava Creek, a short distance 
from Mammoth Hot Springs. 

Whether these records indicate that only Drunella is parasitized by 
Grcgarina, and Heptagenia by a nematode parasite, is conjectural. The records 
are too few to permit any definite conclusions. 

The proportions of plant and animal matter and of unidentifiable detritus 
accord well with the findings of Needham (’20) for midwestern lakes and 
streams. 

The Food of Trichoptera. The following table shows in detail the food 
percentages of the specimens of caddisworms studied. 


254 


Roosevelt Wild Life Annals 
Table No. 5. — Showing Food of Trichoptera. 


Collec- 
tion 
Num- 1 
ber 

Specimen Number 
and Name 

Date, 

1921 

Locality 

5566a 

1. Rhyacophila 

Aug. 10 

Lost Creek .... 

5566h 

1. Thremma 

Aug. 10 

Lost Creek .... 

5566d 

3. Thremma 

Aug. 10 

Lost Creek .... 





5566d 

1. Hydropsyche 

Aug. 10 

Lost Creek .... 

5566d 

2 . Hydropsyche 

Aug. 10 

Lost Creek .... 

5S66d 

3. Hydropsyche 

Aug. 10 

Lost Creek .... 

SS66d 

5. Thremma pupa. 

Aug. 10 

Lost Creek .... 

5566i 

3. Hydropsyche 

Aug. 10 

Lost Creek .... 

556ti 

4* Hydropsyche 

Aug. 10 

Lost Creek .... 

5566i 

5. Rhyacophila 

Aug. 10 

Lost Creek .... 

S566j 

1. Rhyacophila 

Aug. 10 

Lost Creek .... 

5566j 

2. Hydropsyche 

Aug. 10 

Lost Creek .... 

5566j 

6. Rhyacophila 

Aug. 10 

Lost Creek .... 

55661 

3. Rhyacophila 

Aug. 10 

Lost Creek .... 

5 5 661 

4. Rhyacophila 

Aug. 10 

Lost Creek .... 

55661 

5. Hydropsyche 

Aug. 10 

Lost Creek ■ • • ■ 

5587a 

35. Hydropsyche 

Aug. 11 

Yellowstone R . 

5587a 

36. Hydropsyche 

Aug. 11 

Y ellowstone R . 

5587a 

40. Brachycentrus . . . 

Aug. 11 

Yellowstone R. 

5587a 

48. Hvdropsyche 

Aug. 11 

Yellowstone R. 

5587a 

49. Philopotamus? . . . 

Aug. 11 

Yellowstone R . 

5587a 

50. Thremma 

Aug. 11 

Yellowstone R . 

5572a 

2. Hydropsyche 

Aug. 12 

Lost Creek. . . . 





5572b 

1. Hydropsyche 

Aug. 12 

Lost Creek .... 

5572b 

2. Hydropsyche 

Aug. 12 

Lost Creek .... 

5572b 

3. Hydropsyche 

Aug. 12 

Lost Creek. . . . 

5572b 

4. Hydropsyche 

Aug. 12 

Lost Creek .... 

5574a 

1. Brachycentrus.... 

Aug. 13 

Lamar River . . . 


Habitat 


Food in Percentages 


Rocks splashed with spray 
Vegetation consisting of 
Melosira, chiefly. Some 
Gomphonema and Clos- 
terium. 

From Prasiola and Oscilla- 
toria. 


Rotifera, 60; Oscillatoria, 40. 
Melosira, 99; Colpoda, 1. 


Melosira, ioo. 


From shady area 

From shady area 

From shady area 
F rom shady area 
Prasiola and diatoms 


Empty. 

Spirogyra, 50; empty diatom 
shells, 50. 

Melosira, 80; diatom shells, 
17; Closterium, 3. 

Diatom shells, 100. 

Empty. 

Melosira, 95; mixed diatoms. 


Prasiola and diatoms 


5- 


Melosira, 65; mixed diatoms. 


Prasiola and diatoms 

Barrens. Few diatom 

shells. 

Barrens. Few diatom 

shells. 

Barrens. Few diatom 

shells. 

Oscillatoria with trace of 
Melosira. 

Oscillatoria with trace of 
Melosira. 

Oscillatoria with trace of 
Melosira. 


Rapids 


Rapids 

Rapids 

Rapids 


Rapids 

Rapids 

Rapids. Oscillatoria, Pra- 
siola, and Melosira. 
Colpoda and rotifers 
feeding among plants. 


Rocks in rapids. Accumu- 
lations of detritus and 
Melosira. Ameba and 
Colpoda feeding. 

Rocks in rapids. Accumu- 
lations of detritus and 
Melosira. Ameba and 
Colpoda feeding. 

Rocks in rapids. Accumu- 
lations of detritus and 
Melosira. Ameba and 
Colpoda feeding. 

Rocks in rapids. Accumu- 
lations of detritus and 
Melosira. Ameba and 
Colpoda feeding. 

Rapids 


* 5 :>* 

Diatom shells, 100. Gregar- 
ine parasites. 

Rotifers, 1; chiror.omids. 4; 
Melosira, 40; diatoms, 10; 
Oscillatoria, 45. 

Mayfly, 1; ad. Chironomus. 
90 ; Melosira, 5 ; diatoms, 4. 

Mayfly nymph. 30; Chirono- 
mus ad., 60; Melosira. 5; 
diatoms, 5; Gregarina. 

Oscillatoria, 95; diatoms, 5. 

Caddisworm, 30; Chirono- 
mus ad., 30; diatoms, 10; 
Oscillatoria, 30. 

Mayfly nymphs (5). 30; 

Chironomus larvae (10), 
50; Melosira, 15; Oscilla- 
toria. 5. 

Chironomus. 10; stem paren- 
chyma. 15; diatoms (Melo- 
sira chiefly), 15; detritus, 
60. 

Mayfly nymph. 95; sand. 5 - 

Wood fragments, 50; dia- 
toms, 15; detritus, 35. 

Tanypus pupa, 40; shore 
diatoms, 20; lake plank- 
ton. 5; Rhizoclonium, 5; 
detritus, 30. 

Empty. 

Shore diatoms. 50; Triton- 
ema, 5; detritus. 45. 

Ameletus, 25; Ephemerella, 
35; Melosira, 40. 


Glossosoma (?) pupae (3), 
40; Glossosoma (?) larvae, 
10; Ephemerella, is:Chir- 
onomus adult, 25; Melo- 
sira, 20. 

Ephemerella (5). 50; Glosso- 
soma (?), pupa. 35; Melo- 
sira, 10; detritus, 5. 
Gregarina. 

Chironomus (2), 20; caddis- 
flies (6), 65; Melosira, 14; 
sand and detritus. 1. 

Chironomus (2). 50; Chirono- 
mus adult, 45; Melosira, 
3; detritus, 2. Gregar.r.a. 

Caddisflies (7), 75; Acro- 
neuria sp. leg, 7; wood 
fragment, 10; trichop- 
terous pupa, 5; Melosira, 
3. Gregarina 

Trebonema, 20: Cymbella, 
40; Cocconeis, 20; Syne- 
dra, 10; diatoms. 10; Gre- 
garina. 


255 


Food of Trout Stream Insects 

Table No. 5. — Showing Food of Triciioptera. — ( Continued ). 


Collec- 

tion 

Xu Ti- 
ber 

Specimen X'umber 
and Name 

Date, 

1921 

Locality 

Habitat 

Food in Percentages 

5574 a 

2. Brachycentrus. . . . 

Aug. 13 

Lamar River. . . 

Rapids 

Tanytarsus, i . ;Nauplii (?) . 
30; wood fibe u 50. Gre- 
garina. 

5574a 

3. Brachycentrus.... 

Aug. 13 

Lamar River . . . 

Rapids 

Chironomus, 5; mayfly 

nymph, 20; Cocoo. eis, 50; 
Synedra, 20; minor dia- 
toms, 5. Gregarina. 

5574a 

4. Brachycentrus. . . . 

Aug. 13 

Lamar River. . . 

Rapids 

Tanytarsus pupa, 30; Coc- 
coneis, 30; Synedra, 30; 
minor diatoms, 10. Gre- 
garina. 

5574 a 

5. Brachycentrus.... 

Aug. 13 

Lamar River . . . 

Rapids 

Mayfly fragments, 20; Tre- 
bonema, 5; Cocconeis, 65; 
Melosira, 5; minor dia- 
toms, 5. Gregarina. 

5574 a 

6. Brachycentrus. . . . 

Aug. 13 

Lamar River . . . 

Rapids 

Synedra, 50; mixed diatoms, 
10; detritus, 40. Gregar- 

5574 a 

7. Brachycentrus.... 

Aug. 13 

Lamar River. . . 

Rapids 

ina. 

Tanytarsus, 25; Cladophora. 
20; diatoms, 10; detritus, 
55. Gregarina. 

5574 a 

8. Brachycentrus.... 

Aug. 13 

Lamar River . . . 

Rapids 

Mayfly fragments, 30; Melo- 
sira, 20; Cladophora, 20; 
diatoms, 10; detritus, 20. 
Gregarina. 

5574 a 

9. Brachycentrus. . . . 

Aug. 13 

Lamar River . . . 

Rapids 

Mayfly fragments, 10; Coc- 
coneis, 5; Melosira, 65; 
diatoms, 10; detritus, 10. 
Gregarina. 

5574 ^ 

1. Brachycentrus sp. 

Aug. 13 

Lamar River . . . 

Violent rapids 

Tanytarsus pupae, 80; plant 
tissues, 15; diatoms, 5. 
Gregarina. 

5574 b 

2. Brachycentrus sp . 

Aug. 13 

Lamar River . . . 

Violent rapids 

Synedra, 5; detritus, 95. 
Gregarina. 

5574 b 

3. Brachycentrus sp . 

Aug. 13 

Lamar River . . . 

Violent rapids 

Mayfly fragments, 10; dia- 
toms, 1; detritus, 89. 
Gregarina. 

5574b 

4. Brachycentrus sp . 

Aug. 13 

Lamar River. . . 

Violent rapids 

Mayfly fragments, 20; Syne- 
dra, 60; Cocconeis, 10; 
detritus, 10. Gregarina. 

5574 b 

5. Brachycentrus sp 

Aug. 13 

Lamar River . . . 

Violent rapids 

Tanytarsus larvae, 5; Tany- 
tarsus purpae, 15; Syne- 
dra, 10; Cocconeis, 10; 
detritus, 60. Gregarina. 

5574c 

1. Brachycentrus sp 

Aug. 13 

Lamar River. . . 

From Cladophora 

Tanytarsus pupae, 30; Clad- 
ophora, 40; Cocconeis, 25; 
diatoms, 5. Gregarina. 

5574 C 

2. Brachycentrus sp . 

Aug. 13 

Lamar River. . . 

From Cladophora 

Detritus, 5; Cladophora. 70; 
Cocconeis, 20; diatoms, 5. 
Gregarina. 

5574c 

3. Brachycentrus sp . 

Aug. 13 

Lamar River . . . 

From Cladophora 

Cladophora, 85; Cocconeis, 
14; diatoms. 1 . Gregarina. 

5574c 

4. Brachycentrus sp . 

Aug. 13 

Lamar River . . . 

From Cladophora 

Synedra, 5; Cladophora, 30; 
Cocconeis, 60; diatoms, 5. 
Gregarina. 

5574c 

5. Brachycentrus sp . 

Aug. 13 

Lamar River. . . 

From Cladophora 

Cladophora, 85; Cocconeis, 
14; diatoms, 1. Gregar- 

5574c 

6. Brachycentrus sp . 

Aug. 13 

Lamar River . . . 

From Cladophora 

ina • 

Synedra, 4; Cladophora, 20; 
Cocconeis, 75; diatoms, 1. 
Gregarina. 

5575 ^ 

1. Thremma 

Aug. 14 

Tower Creek . . . 

Rapids 

Cocconeis, 5; detritus, 95. 

SS 75 f 

2. Thremma 

Aug. 14 

Tower Creek . . . 

Rapids 

Detritus, ioo. 

5575 g 

1. Rhyacophila 

Aug. 14 

Tower Creek . . . 

Lateral pools 

Rhyacophila (3), 80; detri- 
tus, 20. Gregarina. 

5575 g 

2. Rhyacophila 

Aug. 14 

Tower Creek. . . 

Lateral pools 

Glossosoma (?) pupa, 90; 
detritus, 10. Gregarina. 

5575 g 

3 . Rhyacophila 

Aug. 14 

Tower Creek . . . 

Lateral pools 

Chironomus, 20; mayfly 
caudal setae, 80. 

5585a 

i. Hydropsyche 

Aug. 25 

Lost Creek .... 

Shaded area. X'o vegeta- 
tion. 

Chironomus (3), 10; mayfly 
nymph, 10; Melosira, 75; 
diatoms, 5. Gregarina. 

5585a 

2. Hydropsyche 

Aug. 25 

Lost Creek .... 

Shaded area. No vegeta- 
tion. 

Mayfly fragments, 10; Melo- 
sira, 85; diatoms, 5. 
Gregarina. 

5585a 

3. Hydropsyche 

Aug. 25 

Lost Creek .... 

Shaded area. No vege- 
tation. 

Chironomus, 2; mayfly frag- 
ments, 18; Melosira, 75; 
diatoms, 5. Gregarina. 


Roosevelt Wild Life Annals 


-5 


6 


Table No. 5. — Showing Food of Trichoptera. — (Continued ). 


Collec- 

tion 

Num- 

ber 

Specimen Number 
and Name 

Date, 

1921 

Locality 

Habitat 

Food in Percentages 

5585a 

4. Hydropsyche 

Aug. 25 

Lost Creek . . . . 

Shaded area. No vege- 
tation. 

Chironomus, 5; mayfly frag- 
ments. 10; Glossosoma (?) 
pupae. 20; Hydrachnid, 3; 
Melosira. 60; diatoms. 2. 
Gregarina. 

5585a 

5. Hydropsyche 

Aug. 25 

Lost Creek .... 

Shaded area. No vege- 
tation. 

Melosira, 18; diatoms, 2; 
Glossosoma (?) pupa. 40; 
mayfly fragments, 40. 
Gregarina. 

5585a 

6. Rhyacophila 

Aug. 25 

Lost Creek .... 

Shaded area. No vegeta- 
tion. 

Emptv. Gregarina. 

5585a 

7. Rhyacophila 

Aug. 25 

Lost Creek .... 

Shaded area. No vegeta- 
tion. 

Mayfly fragments. 50; Melo- 
sira, 25; wood fragments, 
20; diatoms, 5. Gregar- 

5585a 

8. Rhyacophila 

Aug. 25 

Lost Creek .... 

Shaded area. No vegeta- 
tion. 

Insect fragments, 100. Gre- 
garina. 

5585a 

9. Rhyacophila 

Aug. 25 

Lost Creek .... 

Shaded area. No vegeta- 
tion. 

Glossosoma (?) pupa. 50; 
wood fragments, 49; Melo- 
sira. 1. Gregarina. 
Rhoicosphenia, 96; Coc- 
coneis, 3; diatoms, 1. 
Gregarina. 

5585a 

10. Glossosoma (?)... 

Aug. 25 

Lost Creek .... 

Shaded area. No vegeta- 
tion. 

55 » 0 a 

11. Glossosoma (?)... 

Aug. 25 

Lost Creek .... 

Shaded area. No vegeta- 
tion. 

Rhoicosphenia. 92; Cocco- 
neis. 8. Gregarina. 

5585a 

12. Glossosoma (?)... 

Aug. 25 

Lost Creek .... 

Shaded area. No vegeta- 
tion. 

Empty. 

558 sa 

13. Glossosoma (?)... 

Aug. 25 

Lost Creek .... 

Shaded area. No vegeta- 
tion. 

Rhoicosphenia. 90; Cocco- 
neis, 4; wood fragments, 
4; mixed diatoms. 2. 
Gregarina. 

5585 a 

14. Glossosoma (?)... 

Aug. 25 

Lost Creek .... 

Shaded area. No vegeta- 
tion. 

Melosira. 95; Cocconeis. 2; 
Synedra, 2; otner diatoms. 
1. Gregarina. 

5585 b 

1. Hydropsyche 

Aug. 25 

Lost Creek .... 

Sunlit areas. Melosira 

predominant. Some 

Oscillatoria and Prasi- 
ola. 

Mayfly fragments. 25; Glos- 
sosoma (?) pupa. 25; 
Melosira, 50. Gregarina. 

5585b 

2. Hydropsyche 

Aug. 25 

Lost Creek .... 

Sunlit areas. Melosira 

predominant. Some 

Oscillatoria and Prasi- 
ola. 

Mayfly fragments, 5; Syn- 
edra, 5; Melosira, 90. 
Gregarina. 

5585 b 

3. Hydropsyche 

Aug. 25 

Lost Creek .... 

Sunlit areas. Melosira 

predominant. Some 

Oscillatoria and Prasi- 
ola. 

Sunlit areas. Melosira 

predominant. Some 

Oscillatoria and Prasi- 
ola. 

Mayfly fragments, 15; dia- 
toms, 2; Melosira, 83. 
Gregarina. 

5585b 

4. Hydropsyche 

Aug. 25 

Lost Creek .... 

Mayfly fragments, 15; Glos- 
sosoma ( ? ) pupa . 1 5 ; M elo- 
sira. 68; diatoms. 2. 
Gregarina. 

5585 b 

5. Hvdropsyche 

Aug. 25 

Lost Creek .... 

Sunlit areas. Melosira 

predominant. Some 

Oscillatoria and Prasi- 
ola. 

Mayfly fragments. 40; Chi- 
ronomus pupa. 5; Perlid 
young (2). 15; Melosira. 
38; mixed diatoms. 2; 
Gregarina. 

5585b 

6. Rhyacophila sp. . . 

Aug. 25 

Lost Creek .... 

Sunlit areas. Melosira 

predominant. Some 

Oscillatoria and Prasi- 
ola. 

Sunlit areas. Melosira 

predominant. Some 

Oscillatoria and Prasi- 
ola. 

Rhyacophila, 50; perlid 
young. 10; mayfly frag- 
ments. 25; Melosira. 15 ■ 

5585b 

7. Rhyacophila sp. . . 

Aug. 25 

Lost Creek .... 

Mayfly fragments, ioo. 
Gregarina. 

5585b 

8. Rhyacophila sp. . . 

Aug. 25 

Lost Creek .... 

Sunlit areas. Melosira 

predominant. Some 

Oscillatoria and Prasi- 
ola. 

Perlid young (3), 60; insect 
fragments, 40. Gregar- 
ina. 

5585b 

9. Rhyacopnila sp.. . 

Aug. 25 

Lost Creek . . . . 

Sunlit areas. Melosira 

predominant. Some 

Oscillatoria and Prasi- 
ola. 

Sunlit areas. Melosira 

predominant. Some 

Oscillatoria and Prasi- 
ola. 

Sunlit areas. Melosira 

predominant. Some 

Oscillatoria and Prasi- 
1 ola. 

Mavflv fragments. 99; Melo- 
sira, 1. Gregarina. 

5585b 

10. Rhyacophila sp. . . 

Aug. 25 

Lost Creek. . . . 

Melosira (small amount), 
100. Gregarina. 

5585b 

11. Thremma 

Aug. 25 

Lost Creek 

l 

Melosira, 50; Cocconeis. 5; 
diatoms. 5; detritus. 40. 


Food of Trout Stream Insects 


2 57 


Table No. 5. — Showing Food of Trichoptera. — ( Continued ). 


Collec- 

tion 

Num- 

ber 

Specimen Number 
and Name 

Date, 

1921 

Locality 

Habitat 

5585b 

12. Thremma 

Aug. 25 

Lost Creek .... 

Sunlit areas. Melosira 
predominant. Some 

Oscillatoria and Prasi- 
ola. 

5585b 

13. Thremma 

Aug. 25 

Lost Creek .... 

Sunlit areas. Melosira 

predominant. Some 

Oscillatoria and Prasi- 
ola. 

5585b 

14. Thremma 

Aug. 25 

Lost Creek .... 

Sunlit areas. Melosira 

predominant. Some 

Oscillatoria and Prasi- 
ola. 

5585b 

15. Thremma 

Aug. 25 

Lost Creek .... 

Sunlit areas. Melosira 

predominant. Some 

Oscillatoria and Prasi- 
ola. 

5585b 

16. Thremma 

Aug. 25 

Lost Creek .... 

Sunlit areas. Melosira 

predominant. Some 

Oscillatoria and Prasi- 
ola. 

5589a 

1. Brachycentrus. . . . 

Aug. 26 

Lamar River. . . 

Strong rapids. From 

moss and Cladophora. 

5589a 

2. Brachycentrus. . . . 

Aug. 26 

Lamar River. . . 

Strong rapids. From 

moss and Cladophora. 

5589a 

3. Brachycentrus. . . . 

Aug. 26 

Lamar River . . . 

Strong rapids. From 

moss and Cladophora. 

5589a 

4. Brachycentrus. . . . 

Aug. 26 

Lamar River . 

Strong rapids. From 

moss and Cladophora. 

5589a 

5. Brachycentrus. . . . 

Aug. 26 

Lamar River. . 

Stong rapids. From 

moss and Cladophora. 

5589a 

6. Brachycentrus. . . . 

Aug. 26 

Lamar River . . . 

Strong rapids. From 

moss and Cladophora. 

5589a 

7. Brachycentrus.. . . 

Aug. 26 

Lamar River. . . 

Strong rapids. From 

moss and Cladophora. 

5589a 

8. Thremma 

Aug. 26 

Lamar River. . . 

Strong rapids. From 

moss and Cladophora. 

5589a 

9. Thremma 

Aug. 26 

Lamar River. . . 

Strong rapids. From 

moss and Cladophora. 

5589a 

10. Thremma 

Aug. 26 

Lamar River. . . 

Strong rapids. From 

moss and Cladophora. 

5589a 

11. Thremma 

Aug. 26 

Lamar River. . . 

Strong rapids. From 

moss and Cladophora. 

5589b 

i. Brachycentrus. . . . 

Aug. 26 

Lamar River . . 

Minor rapids. Decaying 
Cladophora. 

5589b 

2. Brachycentrus. . . . 

Aug. 26 

Lamar River . . 

Minor rapids. Decaying 
Cladophora. 

5589b 

3. Brachycentrus.... 

Aug. 26 

Lamar River . . 

Minor rapids. Decaying 
Cladophora. 

5589b 

4. Brachycentrus. . . . 

Aug. 26 

Lamar River. . . 

Minor rapids. Decaying 
Cladophora. 

5589b 

5. Brachycentrus. . . . 

Aug. 26 

Lamar River . . . 

Minor rapids. Decaying 
Cladophora. 

5589b 

6. Brachycentrus. . . . 

Aug. 26 

J 

Lamar River. . . 

Minor rapids. Decaying 
Cladophora. 


Food in Percentages 


Rhoicosphenia, 10; Cocco- 
neis, 35; Melosira, 10; 
diatoms, 5; detritus, 40. 

Cocconeis, 50; Melosira, 30; 
diatoms, 5; detritus, 15. 


Rhoicosphenia, 5; Cocco- 
neis, 10; Melosira, 10; 
diatoms, 5; detritus, 70. 

Rhoicosphenia, 65; Cocco- 
neis, 15; diatoms, 5; detritus, 

15. 


Cocconeis, 5; diatoms, 5; 
detritus, 90. 


Moss, 90; Cymbella, io. 
Gregarina. 

Chironomus pupae (4), 40; 
Chironomus larva, 5 ; may- 
fly nymph, 30; Clado- 
phora, 10; Cocconeis, 10; 
Cymbella, 3; diatoms, 2. 
Gregarina. 

Trebonema, 50; Cladophora, 
10; Cocconeis, 35; dia- 
toms, 5. Gregarina. 
Chironomus, 15; Clado- 
phora, 5; Cocconeis, 5; 
diatoms, 5; mayfly frag- 
ments, 30; moss fragments, 
30; Epithemia, 10. Gre- 
garina. 

Moss, 40; Trebonema, 30; 
Epithemia, 15; Cocconeis, 
5; Cladophora, 5; dia- 
toms, 5. Gregarina. 
Mayfly fragments, 10; Coc- 
coneis, 30; Chironomus, 5; 
diatoms, 5; Epithemia, 50. 
Gregarina. 

Cocconeis, 14; diatoms, 1; 
Epithemia, 85. Gregar- 
ina. 

Moss, 70; Epichemia, 30. 

Moss, 70; Epithemia, 30. 

Moss, 70; Epithemia, 30. 

Moss, 70; Epithemia, 30. 

Mayfly fragments, 50; Melo- 
sira, 35; Cocconeis, 5; 
Epithemia, 5; diatoms, 5. 
Gregarina. 

Mayfly fragments, 30; Chiro- 
nomus, 5; detritus, 15; 
Cocconeis, 25; Epithemia, 
20; diatoms, 5. Gregar- 
ina. 

Melosira, 10; mayfly frag- 
ments, 20; Chironomus, 5; 
Trebonema, 20; Cocconeis, 
30; Epithemia, 10; dia- 
toms, 5; Gregarina. 
Melosira, 5; detritus, 20; 
Cocconeis, 30; Epithemia, 
40; diatoms, 5. Gregar- 
ina. 

Melosira, 5; Cocconeis, 20; 
Epithemia, 65; diatoms, 
10. Gregarina. 

Ameletus fragments, 40; 
Chironomus pupae, 5; 
Cocconeis, 10; Epithemia, 
40; diatoms, 5. Gregar- 
ina. 


Roosevelt Wild Life Annals 


Table No. 5. — Showing Food of Trichoptera. — (Continued ). 


Collec- 

tion 

Num- 

ber 

Specimen Number 
and Name 

Date, 

1921 

Locality 

Habitat 

Food in Percentages 

5589b 

7. Thremma 

Aug. 26 

Lamar River. . . 

Minor rapids. Decaying 
Cladophora. 

Epithemia, 100. 

5590a 

12. Rhyacophila 

Aug. 26 

Yellowstone R . 

Moderate rapids 

Cladophora, 5; detritus. 95. 

5590b 

5. Rhyacophila 

Aug. 26 

Y ellowstone R . 

Rapids along shore 

Ephemerella fragments. 40; 
Chironomus, 40; Trebon- 
ema. 5; detritus, 15. 

5590b 

6. Rhyacophila 

Aug. 26 

Yellowstone R . 

Rapids along shore 

Wood fragments. 50; Tre- 
bonema, 5; detritus. 45- 

5590b 

7. Rhyacophila 

Aug. 26 

Yellowstone R . 

Rapids along shore 

Insect fragments, 15; detri- 
tus, 85. 

5590b 

8. Rhyacophila 

Aug. 26 

Yellowstone R . 

Rapids along shore 

Trebonema, io; detritus, 90. 

5590b 

9. Rhyacophila 

Aug. 26 

Y ellowstone R . 

Rapids along shore 

Detritus, 50; Trebonema, 20; 
Cladophora, 5; moss 
leaves, 15; wood frag- 
ments, 10. 

5 5 90 b 

10. Rhyacophila 

Aug. 26 

Yellowstone R . 

Rapids along shore 

Chironomus. 20; detritus, 80. 

5590 b 

11. Rhyacophila 

Aug. 26 

Yellowstone K.. 

Rapids along shore 

Insect fragments, 90 Chiro- 
nomus, 10. 

559 ia 

I. Hy drops vche 

Aug. 27 

Tower Creek. . 

Minor rapids 

Insect fragments, 100. 

559 ia 

2. Rhyacophila 

Aug. 27 

Tower Creek . . . 

Minor rapids 

Unrecognizable matter (de- 
tritus?), 100. Gregarina. 

559 ia 

3. Rhyacophila 

Aug. 27 

Tower Creek . . 

Minor rapids 

Insect fragments, 80; detri- 
tus, 20. Gregarina. 

5591 a 

4,5. Rhyacophila 

Aug. 27 

Tower Creek . . . 

Minor rapids 

Detritus, ioo. Gregarina. 

559 ia 

6. Thremma 

Aug. 27 

Tower Creek . . 

Minor rapids 

Detritus, 100. Gregarina. 

5591 a 

7. Thremma 

Aug. 27 

Tower Creek . . . 

Minor rapids 

Detritus. 100. Gregarina. 

5591 a 

30. Rhyacophila 

Aug. 27 

Tower Creek . . 

Minor rapids 

Insect fragments, ioo. 

5591 b 

i. Hydropsyche 

Aug. 27 

Tower Creek . . . 

Strong rapids 

Mayfly fragments, 98; Chiro- 
nomus, 2. 

559 lb 

2. Rhyacophila 

Aug. 27 

T ower Creek . . . 

Strong rapids 

Detritus, ioo. Few Gregar- 

559 lb 

3. Rhyacophila 

Aug. 27 

Tower Creek. . . 

Strong rapids 

Insect fragments, ioo. Few 
Gregarina. 

559 lb 

4. Thremma 

Aug. 27 

Tower Creek . . . 

Strong rapids 

Diatoms, 1 ; detritus. 99. 

559 ib 

5 . Thremma 

Aug. 27 

Tower Creek . . 

Strong rapids 

Diatoms, 5; detritus, 95. 

559IC 

1. Rhyacophila 

Aug. 27 

Tower Creek. . . 

Lateral pool, with moder- 
ate current. 

Detritus, 100. 


Table No. 6. — Showing Summary of Food of Trichoptera. 


Name 


Locality 


Number 

of 

Specimens 


Animal 

Food 


Plant 

Food 


Detritus 


Yellowstone River. 

Lost Creek 

Tower Creek 


Rhyacophila 

Rhyacophila 

Rhyacophila 

Average for 

Hvdropsyche | Yellowstone River 

Hydropsyche Lost Creek 

Hydropsyche Tower Creek 

Average for 

Brachycentrus | Yellowstone River 

Brachycentrus Lamar River 

Average for 

Thremma ! Yellowstone River 

Thremma Lamar River 

Thremma Lost Creek 

Thremma Tower Creek 

Average for 


8 

14 

10 
32 

3 

22 

2 

27 

1 

32 

33 

1 

5 

11 

6 
1 1 


57 

55 

49 

48 

35 

100 

42 

19 

18.3 


5 / 

45 

28 

32 



i> 

35 
8 

9 

45 

20 

98 

36 


3-7 


Food of Trout Stream Insects 


259 


Of the results obtained from the study of the stomach contents of insects, 
those from trichopterous stomachs are perhaps of most interest. Of these 
results the following might be said: (1) Each species must be judged by itself. 
Some species seem to have a large percentage of animal matter in their diet, 
others little or none at all. (2) Those feeding on animal matter are inclined 
to be cannibalistic. (3) Local conditions beget local results. A species may 
have a large animal diet in one locality, and a large plant diet in a different 
locality. (4) About sixty per cent of the caddisworms are parasitized by 
gregarines. It was thought possible to establish a correlation between the 
number parasitized and the amount of animal food taken. Thus, Rhyacophila 
with an animal diet of 49% was parasitized to about 45%, and Hydropsychc 
with an animal diet of 42%, to 60%. In contrast to this, Brachycentrus with 
the much smaller percentage of 18.3 animal matter was parasitized practically 
100%. Hence no correlation can be said to exist. 

The findings of other writers seem to corroborate the foregoing conclusions, 
especially 1, 2, and 3. Thus Muttkowski (T8, p. 442) calls attention to the 
fact that caddisworms readily exchange a phytophagous for a sarcophagous 
diet. Felber (’08) remarks on the avidity of Halesus larvae. These are car- 
nivores, and not only do they not content themselves with smaller animals as 
food, but may even attack larger animals. Thus on one occasion Felber noted 
that some fifteen larvae clung to a Triton in an aquarium. Next day the 
salamander was dead and the skeleton had been practically stripped. 

Lloyd (’21) in a series of detailed studies of various caddisflies brings 
together considerable data as to the food of the larvae. In successive order 
the food is noted for the following species : 

Neuronia postica, stygipcs, and pardalis — leaves in all stages of preservation. 

Phryganca interrupta, and vestita — green plant tissues in natural 
environment, in the laboratory any plant food. 

Limnophilus combinatus — vegetable matter, some diatoms. 

L. indivisus — vegetable matter, without discrimination, decaying tissues in 
greater abundance. 

D. submonilifer — raspings from sticks and plants, diatoms and other 
microscopic organisms, as well as wood or plant fragments. 

Arctoccia consicia — shallow raspings from sticks and vegetation. 

Astcnophylax argus — dead bark and wood. 

Pycnopsyche scabripennis — raspings of decomposed wood. 

Platyphylax designata — young larvae with diatoms ; large larvae with 
diatoms, sand, and fragments of higher plants. Vorhies lists “watercress and 
watermilfoil.” 

Halesus guttifer — fine raspings of decomposed wood. 

Chilostigma difficilis — fragments of wood and leaves. 

Brachycentrus nigrisoma — diatoms at first, then green algae and seed plants ; 
carnivorous at the end of six weeks. 

Mystacides sepidchralis — masticated pulp of vegetable origin. 


Roosevelt Wild Life Annals 


2 6o 


Hydropsychidae — young larvae on green and blue-green algae. Older larvae 
tend to be carnivores. 

Polycentropus — plankton and small insects. 

Rhyacophilidae — filamentous algae and small larvae. 

The last three are the types noted for their animal food in Yellowstone 
Park. It would seem, therefore, that the animal diet of these species is not 
confined to inhabitants of trout streams of the West. 

The Food of Diptera. The following table gives in detail the food 
percentages of the specimens studied. 

Table No. 7. — Showing the Food of Diptera. 


Collec- 

tion 

Num- 

ber 

Specimen Number 
and Name 

Date, 

1921 

Locality 

Habitat 

Food Material Percentages 

5566b 

2. 

Chironomus sp. . . 

Aug. 

IO 

Lost Creek .... 

From Melosira 

Melosira, 50; Cymbella, 50. 

5566 j 

4 - 

Chironomus sp . . . 

Aug. 

10 

Lost Creek .... 

From barrens with a few 
diatom shells. 

Sand, 80; diatoms, 20. 

5566k 

3 - 

Chironomus sp . . . 

Aug. 

10 

Lost Creek .... 

From barrens with a few 
diatom shells. Some 

Closterium. 

Diatoms, 5; sand, 95. 

5 5 661 

6 . 

Chironomus sp . . . 

Aug. 

10 

Lost Creek .... 

Nearly pure Oscillatoria 
with a trace of Melosira. 

Oscillatoria, 95; diatoms. 5. 

556 -a 

I 3 - 

Tipulid larva 

Aug. 

II 

Y ellowstone R . 

Rapids 

Juices of other animals?, 100. 

5567a 

14 . 

Tipulid larva 

Aug. 

1 1 

Yellowstone R . 

Rapids 

Juices of other animals?, ioo. 

5567a 

37 - 

Tany tarsus larva . 

Aug. 

II 

Yellow'stone R . 

Rapids 

Diatoms, 95; sand, 5. 

5567a 

38 . 

Tany tarsus larva . 

Aug. 

1 1 

Yellowstone R.. 

Rapids 

Diatoms, 100. 

5567a 

41. 

Simulium sp 

Aug. 

II 

Y ellow'stone R . 

Rapids 

Shore diatoms, 45; Rhizo- 
clonium, 5; lake plankton, 

5567a 

42, 43, 44, 45. Simu- 
lium sp. 

Aug. 

II 

Yellowstone R. 

Rapids 

Shore diatoms. 45; Rhizo- 
clonium, 5; lake plankton. 

5567 a 

46. 

Simulium sp 

Aug. 

II 

Yellowstone R. 

Rapids 

Shore diatoms, 80; lake 
plankton, 20. 

5567a 

47 - 

Simulium sp 

Aug. 

II 

Y ellowstone R . 

Rapids 

Shore diatoms, 80; lake 
plankton, 20. 

5589 a 

22. 

Simulium sp 

Aug. 

26 

Lamar River . . . 

Strong rapids on moss and 
Cladophora. 

Trebonema. i; diatoms. 60; 
Cladophora, i; detritus, 
38. 

Detritus, 50; diatoms, 45; 
green algae, 5. 

5590 C 

12. 

Simulium sp 

Aug. 

26 

Yellowstone R . 

Strong rapids. Violent 

current. 

5590 C 

13. 14. 15- Simulium 
sp. 

Aug. 

26 

Yellowstone R . 

Strong rapids. Violent 

current. 

Detritus, 50; diatoms, 45; 
green algae, 5. 

5 5 90 C 

16. 

Simulium sp 

Aug. 

26 

Yellowstone R . 

Strong rapids. Violent 
current 

Detritus, 50; diatoms. 45; 
green algae. 5. Parasitized 
by Mermis (?). 

5590 C 

17 - 

Simulium sp 

Aug. 

26 

Yellowstone R.. 

Strong rapids. Violent 
current. 

Detritus, 50; diatoms, 45; 
green algae, 5. Parasi- 
tized by Mermis (?). 


Table No. 8 — Showing Summary of Food of Diptera. 


Name 

Locality 

Number of 
Specimens 

Plant Food 

Detritus 

Chironomids 

Lost Creek 

4 

58 

42 

Chironomids 

Yellowstone River 

2 

97 

3 

Average for 


6 

= 71 

29 

Simulium 

Lamar River 

1 

62 

38 

Simulium 

Yellowstone River 

14 

80 

20 

Average for 


15 

= 79 

21 


Food of Trout Stream Insects 


261 

Probably more than three times the number of specimens listed of both 
chironomids and Simulium were examined, but since the contents were very 
much alike, it was not considered worthwhile to record them separately. What 
is noted here for the food of chironomids agrees in the main with prior data 

recorded by the senior author (Muttkowski, 18, p. 41 1) for species from Lake 

Mendota. The diet comprises primarily the micro-food so abundant in the slimy 
deposits on rocks. 

For Simulium taken from Yellowstone River the large percentage of lake 
plankton is of interest. The source of this is Yellowstone Lake, some forty 

miles above the point where the Simulium were taken. A check made with 

catches from a fine plankton net showed a somewhat similar proportion of lake 
plankton and river algae and diatoms. 

A considerable number of the Simulium were parasitized by a nematode 
(Mermis?) . In the field notes of the senior author, under date of Aug. 15, 
1921, Yellowstone River, the following remarks are relevant: “Simulium taken 

with Mermis (?) emerging. Young Pteronarcys nymphs (black at this stage) 
found feeding among the larvae and pupae. Enemies feeding on Simulium are 
fish and Perlids, and perhaps mayflies. Parasites were found in about one 
third of the larvae.” Another note, dated Aug. 1 1 , is as follows: “All swollen 
individuals (of Simulium ) were parasitized. It was not determined whether 
any pupae were parasitized or if parasitized individuals could pupate. It was 
evident that the Mermis were leaving the larvae for their adult free-living stage. 
Just at what point they left the Simulium larvae was not determined. It was 
noted, however, that the parasite was coiled chiefly at the posterior end of the 
larva, with a small coil near the head.” 

Comparative Summary of the Food of Insects. Even from so brief a study 
as the foregoing certain facts can be gleaned. The most notable point is that 
aquatic insects in rapid streams are opportunists as regards food and eat what- 
ever becomes available. Secondary to this is the fact that the aquatic insects 
forage extensively, and migrate freely in search of food. 

Both of these points become evident from the collections made in Lost 
Creek, where special efforts were made to select various spots in the creek 
for sample collections of food and of specimens in the vicinity or upon that 
food. Reference to the stomach contents of the individual specimens and 
comparison with the food items listed for the particular spot shows at once that 
the large majority of specimens contained food that did not occur within many 
feet of the particular locality. This indicates that these species must be rovers 
and foragers to a marked extent, and that they are opportunists on the whole 
and eat whatever is available. 

Environmental conditions in mountain streams are strenuous ; the strong 
current in particular makes life somewhat precarious and selective feeding 
difficult. Hence as a result the diet becomes diversified : the insects take 
whatever comes along, be it plant, detritus, or animal matter. Their diet thus 
becomes much more generalized than the diet of related species in more per- 
missive habitats, such as ponds and slow streams. In the latter the less strenu- 


26 2 


Roosevelt Wild Life Annals 


ous conditions permit the insects to select their food, that is, to restrict their 
diet to favored food, and to search for that food. 

In other words, specialization of habitat leads to diversification of diet, 
while generalization of habitat permits a restriction of diet. 

The following table gives a comparative summary of the food of the insects 
studied. 


Table No. 9. — Showing Comparative Summary of Food of Insects. (Empty 
Stomachs not Included in the Computations). 


Name 


Number 

of 

Specimens 


Animal 

Food 


Plant 

Food 


Detritus 


Pteronarcys . 
Acroneuria . 
Perla 


Perloidea 

Perloidea 

Perloidea 

Average for . . 

Ephemeroidea. . . 

Ephemeroidea . . . 

Ephemeroidea. . . . 

Ephemeroidea. . . 

Ephemeroidea. . . 

Average for. . 

Trichoptera 

Trichoptera 

Trichoptera 

Trichoptera | Thremma 

Average for 

Diptera | Chironomidae 

Diptera 1 Simulium.... 

Average for 


Ameletus sp . . . 

Baetis sp 

Drunella sp. . . . 
Ephemerella sp . 
Heptagenia sp . 


Rhyacophila. . 
Hydropsyche. . 
Brachycentrus . 


26 
49 

5 
80 

25 

2 

20 

28 

34 

109 

32 

27 

33 

23 

115 

6 
14 
20 


3.85 

77-4 

85 

54 


18 

3 


4-3 

49 

42 

18.3 

28 


53 85 
6-3 
15 

22.3 

22.7 
50 

36.8 

36.3 

24 

29.7 
23 
54-3 

72.7 

64 

54 

71 

79 

76 . 6 


42 

16 


23-7 

77-3 

50 

44-7 

60 

76 

66 

28 
3-7 
9 

36 

18 

29 

21 

23 -4 


LIST OF REFERENCES 

References to food of aquatic insects are exceedingly scant. As a rule they 
consist of brief notations in papers devoted to the biology and metamorphosis of 
aquatic forms. 

Felber, Jacques 

1908. Die Trichopteren von Basel und Umgebung, mit Beriicksichtigung der 
Trichopterenfauna der Schweiz. Arch. f. Naturgesch 74, pp. 80. 

Lloyd, J. T. 

1921. The Biology of North America Caddisflv larvae. Lloyd Librarv Bull. 
21, p. 124. 

Muttkowski, R. A. 

1918. The Fauna of Lake Mendota: A Qualitative and Quantitative Survey 
with Special Reference to the Insects. Trans. Wis. Acad. Sci.. 
Vol. 19, pt. i. pp. 374-482. 

1925. The Food of Trout in Yellowstone National Park. Roosevelt Wild 
Life Bulletin, Vol. 2, No. 4, pp. 470-497. 


Food of Trout Stream Insects 


263 


Needham, J. G. and Claassen, W. C. 

1925. Monograph of Plecoptera or Stoneflies of America north of Mexico. 
Pp. 397. (Am. Ent. Soc. Monographs, Lafayette, Ind.) 

Needham, J. G. 

1920. Burrowing Mayflies of our Larger Lakes and Streams. U. S. Bureau 
Fisheries Bull. 36, pp. 269-292. 

Newcomer, E. J. 

1918. Some Stoneflies Injurious to Vegetation. Jour. Agr. Research, No. 
13- PP- 37-41- 
Wodsedalek, J. E. 

1912. Natural History and General Behavior of the Ephemeridae Nymphs 
Heptagenia interpunctata (Say). Ann. Ent. Soc. Am., No. 
pp. 31-40. 

Wu. C. F. 

1923. Anatomy and Ethology of Nemoura. Lloyd Library Bull. Ent. Ser. 
No. 3, pp. 81. 


IO 







THE ROOSEVELT WILD LIFE MEMORIAL 


As a State Memorial 

The State of New York is the trustee of this wild life Memorial 
to Theodore Roosevelt. The New York State College of Forestry at 
Syracuse is a State institution supported solely by State funds, and 
the Roosevelt Wild Life Forest Experiment Station is a part of this 
institution. The Trustees are State officials. A legislative mandate 
instructed them as follows: 

“To establish and conduct an experimental station to be known as 
‘ Roosevelt Wild Life Forest Experiment Station,’ in which there shall 
be maintained records of the results of the experiments and investiga- 
tions made and research work accomplished; also a library of works, 
publications, papers and data having to do with wild life, together with 
means for practical illustration and demonstration, which library shall, 
at all reasonable hours, be open to the public.’’ [Laws of New York, 
chapter 536. Became a law May 10, 1919.] 

As a General Memorial 

While this Memorial Station was founded by New York State, its 
functions are not limited solely to the State. The Trustees are further 
authorized to cooperate with other agencies, so that the work is by 
no means limited to the boundaries of the State or by State funds. 
Provision for this has been made by the law as follows : 

“ To enter into any contract necessary or appropriate for carrying 
out any of the purposes or objects of the College, including such as 
shall involve cooperation with any person, corporation or association 
or any department of the government of the State of New York or 
of the United States in laboratory, experimental, investigative or 
research work, and the acceptance from such person, corporation, 
association, or department of the State or Federal government of 
gifts or contributions of money, expert service, labor, materials, 
apparatus, appliances or other property in connection therewith.” 
[Laws of New York, chapter 4 2 . Became a law March 7, 1918.] 

By these laws the Empire State has made provision to conduct forest 
wild life research upon a comprehensive basis, and on a plan as broad 
as that approved by Theodore Roosevelt himself. 


Form of Bequest to the Roosevelt Wild Life Memorial 

I hereby give and bequeath to the Roosevelt Wild Life Forest 
Experiment Station of The New York State College of Forestry at 
Syracuse, for wild life research, library, and for publication, the sum 
of , or the following books, lands, etc.