LIMNOLOGICAL EFFECT 5 OF HEADWATER FERTILIZATION ON THE WEST BRANCH OF THE STURGEON RIVER, MECHQGAN ThuisforfhubngmofM.S. MICHIGAN STATE UNWERSITY Peter James Colby 1957 “1.5.51.9? LIBRARY Michigan State University 6M? LIMNOLOGICAL EFFECTS OF HEADWATER FERTILIZATION ON THE WEST BRANCH OF THE ; STURGEON RIVER. MICHIGAN By PETER JAMES COLBY A THESIS Submitted to The College of Agriculture of Michigan State University of Agriculture and Applied Science in partial fulfillment of the requirements . for the degree of MASTER OF SCIENCE Department of Fisheries and Wildlife 1957 V . --n F n p~m A BS TRAC T During the summer of 1955 two applications of inorganic commercial fertilizer were made to Hoffman Lake, the source of the west branch of the Sturgeon River. Following fertilization there was an increase in total and soluble phosphorus. ammonia nitrogen. and possibly sulfates at Station I only. Both in 1954 and 1955 there was an obvious increase in aufwuchs flora at Station I following fertilization. Contrary to the 1954 results, in 1955 the 30-day collections showed a decrease in flora at the downstream stations. This is not in agreement with the reSults of the weekly collections where a statistically significant in— crease was detected following fertilization. Such factors as limited carrying capacity of the shingles. erosion, predation, et cetera, may cause the shingles left in the stream for 30-day periods to lose their efficiency in accumulation of aufwuchs flora. There was approximately a 14 percent increase in the vol- ume of bottom organisms from 1954 to 1955. The average wet weight per square foot values show production to be low in the west branch of the Sturgeon River as compared with other similar str earns . ii There is evidence of longitudinal distribution of trout in the west branch. Starting with brook trout at the headwaters there is a gradual displacement by rainbow and brown trout downstream. The brook trout growth in the west branch is poor, even when com- pared to unproductive streams. iii (‘3 (I! AC KNOWLE DGME NTS The writer wishes to express his gratitude to: Dr. Robert C. Ball. under whose direction this study was made, and Dr. Frank F. Hooper, for their assistance and guidance; Mr. Nickolas Anton, an associate throughout the major part of this investigation; Dr. Gordon Guyer for his assistance with the identification of bottom fauna; Dr. D. W. Hayne for assistance with the statistical prepara- tion and analysis; Dr. E. W. Roelofs and Dr. G. W. Prescott for their helpful criticisms; and Mr. Edward H. Bacon and Mr. Gerald F. Meyers for assistance in the collections of field data. This project was carried out under a graduate research fel- lowship provided by the Agricultural Experiment Station of Michigan State University. 9 The study is sponsored by the Department of Fisheries and Wildlife and the Institute for Fisheries Research. iv TABLE OF CONTENTS INTRODUCTION ............................... LOCATION AND DESCRIPTION OF STATIONS AND STUDY AREA ............................. Application of Fertilizers ...................... Physicochemical ............................. Biological ................................. Aufwuchs ................................ Bottom fauna ............................. Fish samples ............................. RESULTS AND DISCUSSION ...................... Phy sic oche mic al ............................. Phosphorus .............................. Ammonia nitrogen ......................... Sulfates ................................. Hydrogen- ion concentration ................... Conductivity .............................. IO 10 10 11 ll 16 16 18 18 18 24 2.6 28 30 30 Page Biological ................................. 39 Aufwuchs flora ............................ 39 Aufwuchs faunae .......................... 46 Bottom fauna . ............................ 53 Fish samples ............................. I 64 SUMMARY ................................... 73 LITERATURE CITED ........................... 76 i APPENDIX .................................. 80 "" i vi TABLE II. III. IV. VI. VII. LIST OF TABLES Discharge (volume of flow) Measurements Taken from the West Branch of the Sturgeon River on July 23, 1954, and August 27, 1955 . . . . Parts per Million of Phosphorus in Water Samples Taken from the West Branch of the Sturgeon River during the Summer of 1955 ............................... Parts per Million of Ammonia Nitrogen in Water Samples Taken from the West Branch of the Sturgeon River during the Summer of 1955 ............................. Parts per Million of Sulfates in Water Samples Taken from the West Branch of the Sturgeon River during the Summer of 1955 ............................. Parts per Million of Methyl Orange Alkalinity in Water Samples Taken from the West Branch of the Sturgeon River for the Summer of l 955 ....................... The Hydrogen-Ion Concentration of Water Samples Taken from the West Branch of the Sturgeon River during the Summer of 1955 ............................... Conductivity (in Mhos x 10-6 at 18°C) of Water Samples Taken from the West Branch of the Sturgeon River during the Summer of l 955 ....................... vii Page 23 2.5 27 29 31 32. .;l TABLE Page VIII. Analysis of Variance of Changes in the Density of Chlorophyll Extracted from Aufwuchs Attached to the Bricks. Excluding Stations I and A ................ 41 IX. Analysis of Variance of Changes in the Density of Chlorophyll Extracted from 7 Aufwuchs Attached to the Shingles. . Excluding Stations 1 and A ................ 41 X. Analysis of Variance of Changes in the Density of Chlorophyll Extracted from Aufwuchs Attached to the Shingles at . StationIVA............: .............. 43 .._ XI. Analysis of Variance of Changes in the Density of Chlorophyll Extracted from Aufwuchs Attached to the Shingles at Station A ............................. 43 XII. A Comparison of the Aufwuchs Fauna (mean number per substrate) Taken from the West Branch of the Sturgeon River during the Summers of 1954 and 1955 ........ 52 XIII. Taxonomic Composition and Enumeration of the Bottom Fauna Sampled from the West Branch of the Sturgeon River ......... 54 XIV- Composition by Percent of the Number of Bottom Fauna Sampled from the West Branch of the Sturgeon River for the Summer of 1955 ........................ 57 XV. Analysis of Variance of Numbers of Bottom Fauna Samples from the West Branch of the Sturgeon River for the Summer of 1955 ......................... 61 viii . .tl . I TABLE XVI. XVII. XVIII. XIX. XXI. Page Condensation of the Number and Volume of Bottom Fauna Sampled from the West Branch of the Sturgeon River for the Summer of 1955 ........................ 63 Composition and Enumeration of Trout Samples from the West Branch of the Sturgeon River Using a Direct Current Shocker .............................. 65 A Comparison of the Mean Length in Inches of Trout Samples from the West Branch of the Sturgeon River, July 6. 1954, and 1955 ......................... 66 Regression (covariance) Analysis of 1n Length—1n Weight Relationship in Brook Trout Taken from the West Branch of the Sturgeon River, 1954 and 1955 . . . ......... 69 Regression (covariance) Analysis of 1n Weight—1n Weight Relationship in Brown Trout Taken from the West Branch of the Sturgeon River, 1954 and 1955 ........... 70 Regression (covariance) Analysis of In Weight—1n Weight Relationship in Rainbow Trout Taken from the West Branch of the Sturgeon River. 1954 and 1955 ........... 71 ix LIST OF FIGURES Figure Page 1. Average monthly water temperature of the west branch of the Sturgeon River and its tributaries for the v summer of 1955 ..................... . . . . 5 i 2.. Comparison of the total phosphorus content of water samples taken from the west branch of the Sturgeon River 4 ~ - during the summers of 1954 and 1955 ......... l9 ' 3. Graphic representation of the hydrogen- ion concentration, methyl orange alka- linity. and conductivity of water samples taken from the west branch of the Sturgeon River during the summer of 1955 ................................. 33 4. The percentage composition of the aufwuchs fauna .......................... 48 5- A comparison of the numerical abundance of bottom fauna collected during the summers of 1954 and 1955 ................. 59 .4 x p cm I“ ci INTRODUC TION Fishing continues to be a leading attraction in the state's multimillion dollar tourist industry, and according to economists. this industry will continue to grow (Michigan Department of Conser- vation, 1955). Thus the maintenance and improvement of the exist- ing fisheries becomes important. A means of improving the available recreational fisheries would be the development of prac- tical methods to increase the biological productivity of our less productive lakes and streams. This dissertation deals with the second-year phase of a four- year project designed to test whether trout fishing can be improved in an unproductive trout stream by the addition of nutrients, and also to determine if it is economically feasible to use this method as a management procedure. The second~year study consists of evaluating the data collected during the summer of 1955 and making comParisons where possible with the information obtained in 1954 by Grzenda (1955). In conjunction with the stream studies. disserta- tions by Alexander (1956) and Anton (1957) deal with the fertilization 0f Hoffman Lake. Fertilization as a management procedure in streams and larger lakes is still in the experimental phase. Hasler and Einsele (1948) pointed out that detrimental effects of fertilization may out- weigh biological gains; thus. they strongly emphasized that only ex- perimental fertilization should be undertaken at this stage of our __ ._-.—._4Aol knowledge. They concluded that apart from increasing productivity. addition of nutrients to a lake gives the limnologist an excellent tool for studying lake metabolism experimentally. Almost all of the fertilization projects to date have been limited to lentic environ— ments such as farm ponds and small lakes. A recent review of the literature on artificial fertilization of lakes and ponds is given by Maciolek (1954). The application of commercial inorganic fertilizer to Hoffman Lake which feeds the west branch of the Sturgeon River is one of the original attempts to enrich a lotic environment. One other at- tempt has been recorded by Huntsman (1948) who added commercial 1“organic: fertilizer to a barren Nova Scotia stream and found an in- crease in the quantity of fish. filamentous algae, and certain insect larvae. LOCATION AND DESCRIPTION OF STATIONS AND STUDY AREA The west branch of the Sturgeon River is located in Charle- voix. Otsego. and Cheboygan counties in the northern Lower Penin— sula of Michigan. It arises from Hoffman Lake (T.32N,R.4W sec. 26,27,34,and35) and flows in a northeasterly direction for approxi- mately thirteen miles. joining the Sturgeon River at Wolverine. The tributaries are Allen. Berry. and Fulmer creeks. The west branch receives a large volume of ground-water seepage and spring flow. as can be seen from the discharge meas- urements (Table I). which probably accounts for the relatively stable water temperature (Figure 1). The watershed is located in the interlobate area of the Port Huron Morainic System formed during the Mankato substage of Pleistocene glaciation. Whiteside. Schneider. and Cook (1956) clas- sify this area as that of Land Division N of the limy Podzol Region Of Michigan. They characterize this division as a rolling to ex- tremely rough land which occupies the morainic areas of the northern part of the Lower Peninsula and the eastern part of the Upper Pen- insu1a_ The parent materials from which the soils of this area were 3 II TABLE I DISCHARGE (VOLUME OF FLOW) MEASUREMENTS TAKEN FROM THE WEST BRANCH OF THE STURGEON RIVER ON JULY 2.3. 1954. AND AUGUST 27. 1955a t w v—f vv—v—f fififi v4 v—v v—v—V Discharge (C FS) Station as L {EL- 1954 1955 . II 8.76 6.56 111 9.68 --- IV 16.5 --- . ___ V 21.0 23.2 VI 29.6 --- VII - 45.2 -..- VIII --- 68.3 1 - - al954 data courtesy of Arlington D. Ash. USGS. Lansing. Michigan. U1 Figure 1. Average monthly water temperature of the west branch of the Sturgeon River and its tributaries for the summer of 1955. AOL "chansons-5H. 1 t S mum. uuu i JJA __ ._.. - x. __ IA Alfixluut . . / k/k // / /. _gq d a q — didq—d _ u—l’fin munuumwmnmmmnmm9 1 Berry I Creek Creek VII VIII Fulmer II III IV V VI A Stations formed range from sands to sandy loams. with loams and clay loams in local areas. The original forest was chiefly hardwood with the sugar maple (Acer sacchrum) the dominant tree. The value of the land for farming is greatly reduced by the associated sandy soils and unfavorable slopes. Due to the high relief of the adjacent moraines the watershed is rather restricted. Grzenda (1955) approximated the drainage area of the watershed to be 14.0 square miles. The vegetation adjacent to the stream is largely composed of stands of aspen (Populus sp.). red cedar (Juniperus virginiana). black spruce (Picea mariana). and tag alder (Alnus incana). The following is a brief description of eight collections and the one control station used to study the effects of dilution of the added nutrients and their utilization at varying distances downstream from the lake. Station I: This station is located at the outlet of Hoffman Lake. the source of the west branch of the Sturgeon River. The outlet is narrow and only a small volume of water leaves the lake. The bottom is composed of marl and the physicochemical and bio- logical conditions are more typical of the lake than the remaining downstream stations. The higher aquatic plants consist of Potamogeton spp.. Typha latifolia. Scirpus sp.. Chara sp., and Sag- E'Earia latifolia. Station 11 is located approximately one mile downstream from Hoffman Lake. There is greater discharge at this station due to the addition of water of two large springs. one of which served as the control station (Station A). The bottom is a combination of shifting sand and silt. Station 111 is. located approximately two miles from Hoffman fivw—vv—v raw—f Lake. The current is slow with the bottom consisting of silt due to partial impoundment of the stream by a beaver dam. There is an abundance of higher aquatic at this station. Nasturtium officinale. Ranunculus longirostris.§Pa£§§_nium sp-. Potamoggtgn SPP- Station IV is approximately four and one-half miles down- stream. The stream here is moderately swift and the bottom is composed mostly of shifting sand and stretches of gravel. This section of the stream receives very little direct sunlight due to the tree canopy. gaffe}? V. VI. and VII are located downstream from the source six and one-half. eight. and nine and one-half miles. re- speCtiVely. The current is moderately swift at these stations. All have the stream bottom covered with patches of sand and gravel. There is a gradual widening of the river from source to confluence with the Sturgeon River. The lower stations receive much more direct sunlight than the upper ones. Station VIII is approximately ten and one-half miles down- stream. One of the large tributaries (Fulmer Creek) enters the west branch here. The bottom is gravel and rubble. No stations were established beyond this point because domes- tic waste from streamside cabins might interfere with the interpre- tation of re sults. METHODS AND PROCEDURES Application of Fertilizers During the summer of 1955. two applications of inorganic j commercial fertilizer (1242-12 N-PoK) were made to Hoffman Lake. Nitrogen and phosphorus were in the form of ammonium sulfate and phosphoric acid respectively. The fertilizer was applied from a '_ j ,- motorboat along the southwestern perimeter of the lake. The lake is unstratified and has complete circulation; therefore. the adding of fertilizer on the windward side distributes the nutrients throughout the lake. following which. if they remain in solution. they may be discharged into the outlet on the eastern end of the lake. The re- sult: possibly the enrichment of the west branch of the Sturgeon River. thus providing the nutrients necessary for primary production at the lower trophic levels. Six thousand pounds of fertilizer were applied July 31 and 4,000 pounds additional on August 6. This was twice the concentration of that added in the two 1954 applications. Physic ochemic a1 Amfilyses of water were made from samples collected at each station to ascertain se1ected physicochemical properties and to trace IO 11 any movement of the nutrients downstream. Total and soluble phosphorus determinations were by the molybdate method (Ellis. Westfall. and Ellis. 1948). ammonia nitrogen by direct Nessleriza- tion. and sulfate by the turbidimetric method (Standard Methods. 1955). The colorimetric determinations used in these procedures were made with a Klett-Summerson photoelectric colorimeter. Al- kalinity was determined by the methyl orange indicator method ac-. cording to Standard Methods. pH was determined electrometrically with a Beckman pH meter. and conductivity. with a conductivity bridge manufactured by Industrial Instruments Company. Water and air temperatures were taken directly with a pocket thermometer at the time the samples were collected. The stream flow or discharge in 1955 was determined by use of Embody's formula (Lagler. 1952). Stream flow determinations in 1954 were provided through the cour- tesy of A, D. Ash. U.S.G.S.. Lansing. Michigan Biological iufwuchs. In the literature there are several definitions of "Periphyton" (the closest English equivalent to the German term "aufwuchs"). Young (1945) found the periphyton complex to be com- prised of organisms with a rather large taxonomic diversity. He describes Periphyton as an "assemblage 0f organisms growing upon M 12 the free surface of submerged objects in waters. and covering them with a slimy coating." He excludes benthos from his definition. The term ”aufwuchs" has a much broader connotation than periphy- ton. "Aufwuchs comprises all attached organisms (except the macrophytes). including such. forms as sponges and Bryozoa. which are usually considered as benthos by American authors; also included are the various forms living free within the mat of sessile forms" (Ruttner. 1953). The assemblage of organisms that collected on the measuring devices placed in the stream will be referred to in this dissertation as aufwuchs following the definition of Ruttner. Patrick (1949) found that the measure which uses largely the organisms that are attached to the bottom or edges of the stream. reflects the water conditions which have flowed by a given point for a considerable time before sampling. whereas a chemical analysis can only describe the condition of the water at the exact time it was taken. A modification of the Harvey (1934) method. rather than the Count method. was used to measure quantitative changes in aufwuchs producation. The lattermethod is time-consuming. very difficult, and 0f doubtful quantitative value. Aufwuchs production was used as an index of productivity mainly because the sterile characteristics of the stream limits the l3 selection of other indices. The aufwuchs community was also used because it is one of the most stable groups of organisms in the lotic environment. Unlike stream plankton. its sessile character- istics protect it from the flushing action of the stream in times of high water. Harvey (1934) found that a good correlation existed between colorimetric determinations of pigment extracted with acetone and the actual enumeration of comparable samples of plankton._ This method was later used by Tucker (1949) as a means of estimating the abundance of phytoplankton. Tucker concluded that in a single sample the method is of little value because the standard error of estimate is too large to obtain a reliable result. However. because of its high correlation with actual counts when many samples are considered, this method is of value as a means of estimating changes in total abundance of phytoplankton. (From the standpoint of statis- tical analysis it has not been perfected sufficiently to be used other than as a general indicator (Tucker. 1949). even With the use Of a PhOtOelectric colorimeter (Tucker. 1956)- Tucker (1949) 3180 found that the highest correlation was among the green algae and diatoms. Which comprise most of the aufwuchs flora in this study. To collect aufwuchs and measure trends in its production. five bricks and fifteen shingles were placed in the stream at each l4 station for thirty-day periods before and after fertilization. At the termination of the first thirty-day period (the day before the first application of fertilizer) the bricks and shingles were removed and new ones placed in the same spot and position. thus enabling the samples to be compared statistically. In addition to the bricks and shingles in the stream. ten shingles were placed upstream from Station IV (Station IVA). The purpose for this procedure was to detect weekly changes in aufwuchs production. The bricks were cinder building bricks 7.9 x 3.7 x 2.3 inches. and the shingles were cedar with 12.0 x 13.0 x 0.3 inch dimensions. The bricks were suspended in the water by means of a wire fastened to a stable object. and the shingles were nailed to logs or other suitable objects in the stream. Care was taken to place the bricks and shingles so that organisms could become attached to all sides. and deep enough that a drop in water level would not leave them exposed to the air. When removed. the bricks were immedi- ately Placed in a porcelain pan to avoid any loss of motile organ- isms. The bricks were then Scrubbed with a nylon brush and washed several times to remove all attached materials. The con- tents of the pan were then poured into a quart glass jar bearing the 15 serial number of the brick. The shingles were placed directly into a plastic bag and the attached materials were later removed in the laboratory. At the laboratory the invertebrate faunae were picked from the samples and preserved in 10 percent formalin. The water was removed by use of the Foerst plankton centrifuge. The outflow tube of the centrifuge was placed in a quart jar to catch the outflowing water. This was necessary because often the samples had to be centrifuged more than once to clear the water of all suspended ma- terial. The mixture of silt and plant material left in the revolving bowl was placed in a bottle. and 95 percent alcohol was added to extract the chlorophyll. The samples at this point contained a supernatant liquid composed of alcohol and extracted chlorophyll. and a residual layer of silt and plant material on the bottom. The mixture was filtered. the filtrate brought to a constant volume. and the density of the extracted pigment was measured colorimetrically With a Klett-Summerson photoelectric colorimeter using a No. 66 (Nd) filter. This gave readings in Klett units which were converted into Harvey units by a graph prepared as follows: One Harvey unit equals 2.5 mg. potassium chromate and 430 mg. nickel sulfate dis- solved in one liter of water (Harvey. 1934). The Harvey standards Wer e Prepared by dissolving 2.5 grams of potassium chromate and 16 43 grams of nickel sulfate in one liter of water. This gave a standard equal to 100 Harvey units. which was diluted to obtain de- sired concentrations used in preparing the graph. Bottom fauna. Bottom samples were collected from relatively uniform riffle areas from June 24 to August 25, 1955, using a Surber square-foot sampler. The sample spots were not randomized but were selected by choosing three transects across the stream and taking four samples at evenly spaced intervals along each transect. thus representing a 12-square-foot sample of stream bottom per week. The invertebrate faunae were picked while alive from the debris and preserved in 10 percent formalin. Fish samples. Fish samples consisted of brook trout (Sil- Vilinus fontinaliS). brown trout (Salmo trutta). and rainbow trout (Salmo gairdnerii). The samples were collected twice during the Summer (July 6 and August 30) at stations 11. V. and VIII using a 2?-0-volt, direct—current shocker. Scale samples. measurements in length to the nearest tenth of an inch, and weight in grams were taken from all sizes and species of trout collected. to determine the weight-length relationship and average length per year class. The Scales were Cleaned and mounted on microscope slides using gem"in”g‘lycerine media. A scale projector was used in determining 17 the average length of each year class. The length-weight relation- ship was computed using the following formula (Rounsefell and Everhart. 1953): W = an in which W = weight L = length c and n = constants or expressed logarithmically. logW=logc+nlogL The values of the constants c and n may be determined by fitting a straight line to the logarithms of L and W (Rounsefell and Everhart. 0p. cit.). Natural logarithms (in) were used to express the relation- ship in this study. RESULTS. AND DISCUSSION Physicochemicgl Phosphorus. Following fertilization there was an increase in total and soluble phosphorus for both 1954 and 1955 (Fig. 2). No significant difference in the concentration was detected at the down- stream stations. Although an increase in total phosphorus was de- tected in the control stream on August 3, it was not of a magnitude as the samples measured at Station I (Table II). Total phosphorus remained at a higher level than the prefertilization concentrations after the second (1955) application. The same situation existed in Hoffman Lake (Anton. 1957). Anton believed that phosphorus became fixed in insoluble precipitates which remained in suspension due to the turbulence of the water caused by wave action and underwater currents. It appears that similar physical forces were responsible for the same effect at Station I in that this station is located at the outlet of Hoffman Lake. Soluble phosphorus increased to 21 p.p.b. on August 3, but rapidly returned to prefertilization concentrations (Table II). This is not unusual for phosphorus may be lost to bottom deposits (Welch. 18 .A’li 19 Figure 2. Comparison of the total phosphorus content of water samples taken from the west branch of the Sturgeon River during the summers of 1954 and 1955. 20 STATION I . .b. 38: ——--1954 1955 601’ 50.1 40. 30.. 20-1 10-4 20- STATION A 15 a 10‘ 5-4 / 15 10 STATION 11 0 15 STATION IV A 10 ..~ ‘ "\ I 5 » ‘v \- \ o .1 l J- l- a L n J A LLJ if; n :1” LA A A4; 1 l A . n l n . mg 4 I0 20 30 9- 19 29 6 July August Sept. Dates of Fertilization: July 30 and August 9. 1954 July 31 and August 6. 1955 a . I..M iii-L:- - -‘ 21 Figure 2 (Continued) 22 STATION V v—v— ‘P‘w-..~:rn — 15~i STATION VII 10-. ‘ .A‘ ref“. ’..--.. 5. r V ‘4 01......- -- -,__ ,L- - - - - -- _. -.. l 15" STATION VIII 10- A A 5g ” \" ‘ J ‘ v - "' Dirt—+10 20 0.1...L-4...s.-$-.I-i-.i--I., §.L._L.L.4219....L_LJ—-I—z July August Sept. Dates of Fertilization: July 30 and August 9. 1954 July 31 and August 6, 1955 r—-1 23 TABLE II PARTS PER BILLION OF PHOSPHORUS IN WATER SAMPLES TAKEN FROM THE WEST BRANCH OF THE STURGEON RIVER DURING THE SUMNIER OF 1955a " V 1w v—vfiv—v fl Station Date Item H s m - -c- I A II III IV V VI VII VIII 1 July 7 Soluble 1 1 1 1 l l 1 1 l j Total 6 3 4 4 4 4 3 6 6 ‘ 1 l Soluble 2 tb 1 l 1 l l 1 1 Total 6 3 3 3 3 3 3 3 1 8 Soluble t t t t t t t t t Total 7 6 6 8 8 7 5 8 7 2 8 Soluble 1 5 l l l 1 l l 1 Total 1 1 5 7 8 8 8 6 6 6 Aug. 3 Soluble 2 l 1 t t 3 2 t Total 5 1 8 7 1 2 7 8 1 0 1 1 9 7 Soluble l 0 .. . . . . . . Total 2 2 5 7 7 6 6 5 5 5 9 Soluble . . . . . . . . . . . Total 2 4 5 6 5 5 5 6 5 5 1 l Soluble 3 0 t 1 1 2 t t 1 Total 3 3 5 7 8 7 8 7 6 6 1 3 Soluble 2 1 1 3 1 1 l t t Total 3 0 4 7 8 7 7 7 8 8 1 7 Soluble 1 t l t 0 t 0 it t Total 2 8 6 12 8 6 7 7 7 7 2 2 Soluble 2 2 z z 2 2 l 2 1 Total 2 6 8 8 9 9 8 9 7 7 7- 6 Soluble 1 1 1 1 l 1 l 1 1 Total 2 1 6 8 7 7 7 6 6 6 IE”Dates of fertilization: July 31 and August 6. b1: =2 trace amounts below 1 p.p.b. 24 1952). taken up by plants (Ruttner. 1953), or precipitated out in some chemical compound such as tricalcium phosphate (Neess. 1949). It was discovered that radioactive phosphorus (P32) is taken up by plants and zooplankton in a matter of minutes or hours. not days or weeks (Coffin _e_t_a_l., 1949). Moyle (1954) describes the phosphorus optimum for lake trout (in Minnesota waters) to be 0.02 p.p.m. A comparison of his value with those measured in the west branch indicates that the concentra— tion of phosphorus in the stream is too low for a very successful is» salmonoid environment. At the time of fertilization it was estimated that less than 1 cu. ft./ sec. of water left Hoffman Lake at Station I as compared to 6.6 cu. ft./sec. leaving Station 11. Since the greatest source of waters at Station 11 are the springs and ground water seepage, it is assumed that the phosphorus concentration was greatly reduced by dilution. Ammonia nitrogen. A temporary increase in ammonia nitro- gen Was detected at Station I on August 3 (Table III). This may have been the result of fertilization due to peak concentrations being measured in Hoffman Lake on that date (Anton. 1957)- N0 quanti- tative increase that could be attributed to fertilization occurred TABLE III PARTS PER MILLION OF AMMONIA NITROGEN IN WATER SAMPLES TAKEN FROM THE WEST BRANCH OF THE STURGEON RIVER DURING THE SUMMER OF 19553 Station Date s . I A II III IV V VI VII VIII June 29 .04 .02 .02 .02 .00 .07 .ll .02 .04 July 7 .02 .02 .02 .02 .02 .02 .04 .02 .02 ll .04 .01 .01 .07 .04 .05 .15 .03 .04 18 .14 .06 .03 .07 .09 .08 .07 .06 .06 28 .07 .02 .03 .05 .05 .04 .04 .03 .03 A b ugust 2 t t -t t t t t t t 3 28 t t t t t t t t 7 0 0 0 0 0 O 0 0 O 11 .10 .10 .15 .15 .10 .20 .20 .15 .20 17 .02 .02 .02 .03 .02 .02 . .02 .02 .03 22 .01 .01 .01 .01 .01 .01 .01 .01 .01 26 t t t t t t t t t 8‘Dates of fertilization: July 31 and August 6. b t = trace amounts. 26 downstream. Although increases in ammonia nitrogen were detected downstream on August 11, a similar trend was observed in the control stream. It is also conceivable that a concentration of .20 p.p.m. may occur naturally in the west branch. This reasoning is based on the concentrations which approached .20 p.p.m. prior to fertilization (Table III). The rapid decrease of ammonia may have been the result of oxidation of ammonia nitrogen into the nitrite and nitrate forms. Barnes (1955) states there is strong evidence that ammonia is oxi- dized to nitrite and subsequently to nitrate. He states further that the nitrate form is largely taken up by the diatoms. Ammonia salts in excess are reported as poisonous to fishes if present with carbonates (Welch. 1952). Amounts exceeding 2.5 P-p-m. are generally detrimental or lethal, and quantities of more than 1.0 p.p.m. usually indicate organic pollution (Ellis 3:31., 1948). Table III shOws the values for ammonia nitrogen to be low. indicat- ing little organic production in the west branch of the Sturgeon River . Sulfates. There were slight variations in the amount of sul- fate Present at all stations. The highest concentration of 17 p.p.m. was observed at Station I on August 3 and 9 (Table IV)- The TABLE IV PARTS PER MILLION OF SULFATES IN WATER SAMPLES TAKEN FROM THE WEST BRANCH OF THE STURGEON RIVER DURING THE SUMMER OF 1955a 27 Station Date - I A 11 HI IV V VI VII VIII. June 20 14 l3 l3 13 12 11 ll 11 22 15 10 13 13 12 12 ll 10 10 27 13 10 12 ll 11 11 10 9 10 29 14 10 12 12 12 12 10 10 9 July 5 13 8 11 ll 9 9 8 8 9 ll 14 10 12 12 ll 11 10 10 10 18 14 10 11 l3 13 13 12 10 10 25 14 10 13 12 13 12 11 11 12 August 2 l3 9 12 11 ll 11 10 9 9 3 17 10 12 12 12 11 10 10 10 7 13 9 10 12 .13 11 12 ll 10 9 l7 9 13 12 12 11 10 11 11 ll 15 9 12 ll 11 10 11 10 ll 13 15 ll 12 12 12 12 11 9 10 17 14 10 12 12 13 11 9 9 9 22 16 9 12 13 12 12 11 11 ll 26 16 8 10 11 ll 11 10 9 9 a 0 Dates of fertilization: July 31 and August 6. I. “.1 I? n‘ 28 August 3 high may have been the result of fertilization in that a concentration of 26 p.p.m. was present in Hoffman Lake on that date (Anton, 1957). It is also quite conceivable that the quantity (17 p.p.m.) could occur naturally in the stream. Other than to follow the dispersal of fertilizer. sulfate de- terminations provide an index to measure productivity. Studies in Minnesota show a paucity of higher aquatic plants below 50 p.p.m., and the best growth Occurs where the sulfate-ion concentration ex- ceeds 200 p.p.m. (Moyle, 1954). Comparing Moyle's values with those in Table III affords further evidence that production is low in the west branch of the Sturgeon River. Alkalinity. There was no alkalinity as shown by phenolphtha- lein. Therefore, the methyl orange alkalinity is representative of the total alkalinity. Under such conditions the alkalinity is all bi- carbonate (Theroux 3:31., 1943). Alkalinity in the west branch is Probably present) as calcium and magnesium bicarbonate, making the stream an efficient buffer system. Table V shows no change as a result of fertilization. This provides further evidence that the strearn is well buffered. The lower bicarbonate values obtained at Station I are typical 0f Hoffman Lake rather than the downstream stations. This is true TABLE V PARTS PER MILLION OF METHYL ORANGE ALKALINITY IN WATER SAMPLES TAKEN FROM THE WEST BRANCH OF THE STURGEON RIVER FOR THE SUMNIER OF 1955a Z9 _._ 4:. Station Date - 7- I A II III IV V VI VII VIII June 20 150 180 180 180 184 182 180 182 22 155 200 179 182 182 187 185 183 186 27 153 192 178 180 183 185 183 181 186 29 155 187 180 180 180 181 175 177 182 July 7 145 185 160 160 165 165 163 164 169 11 145 187 180 183 180 186 182 181 185 18 142 182 175 168 160 166 161 165 166 25 140 185 176 166 170 175 172 175 179 August 7 130 187 178 177 177 179 177 176 177 9 135 188 176 178 179 180 179 180 182 13 I 136 185 174 173 176 188 187 183 188 17 136 188 184 183 184 188 186 187 188 22 133 187 182 182 183 184 184 182 186 26 134 189 187 187 186 188 187 188 189 8‘Dates of fertilization: July 31 and August 6. 30 due to the stream receiving the major portion of its volume from springs and ground water seepage which are rich in bicarbonates (example. the control stream). HydrcggI-ion concentratign. Variations in pH were small at any one station (Table VI). Because bicarbonates (acting as buffers) ”m react in such a way as to maintain equilibrium. it is conceivable that the effects of fertilization would not be detected by the hydrogen- ? ion concentration. It is the writer's opinion that this situation ex- isted at Station I where values for pH show no significant change. although the effects of fertilization are apparent. It may be of interest to note that by applying the values ob- tained for pH and bicarbonate alkalinity to a carbon dioxide, alkalinity- PH conversion chart (Theroux 3:31., 1943) the quantity of free carbon dioxide in the west branch is negligible. Conductivity. The application of fertilizer had no effect on this measurement. At first it may appear that the decrease in con- ductivity was brought about by fertilization. but the control stream also shows the trend (Fig. 3., Table VII). The variations in con- centration of electrolytes may have been the result of dilution caused by runoff from rainfall. TABLE VI 31 THE HYDROGEN-ION CONCENTRATION OF WATER SAMPLES TAKEN FROM THE WEST BRANCH OF THE STURGEON RIVER DURING THE SUMMER OF 19553 aDates of fertilization: July 31 and August 6. :1 Station Date s -- I A II III IV V VI VII VIII June 21 8.5 .. 8.1 8.5 8.5 8.4 8.4 8.4 8.3 22 8.1 7.8 7.9 8.1 8.1 8.1 8.1 8.1 8.0 27 8.2 7.8 8.0 8.4 8.3 8.3 8.4 8.2 8.2 29 7.6 8.0 8.1 8.4 8.4 8.4 8.4 8.4 8.3 July 7 8.2 7.9 8.1 8.2 8.3 8.2 8.2 8.2 8.2 11 8.1 8.0 8.0 8.1 8.2 8.1 8.1 8.1 8.2 18 7.8 8.0 8.0 8.2 8.2 8.1 8.2 8.1 8.2 28 8.3 8.0 8.2 8.4 8.4 8.4 8.4 8.4 8.3 August 7 8.0 7.7 7.9 8.0 8.0 8.1 8.2 8.2 8.2 13 8.4 7.8 8.2 8.3 8.4 8.3 8.3 8.3 8.3 17 8.2 7.8 8.1 8.2 8.3 8.2 8.3 8.3 8.3 _ 0 n 32 TABLE VII CONDUCTIVITY (IN Nlhos x 10'6 AT 18°C) OF WATER SAMPLES TAKEN FROM THE WEST BRANCH OF THE STURGEON RIVER DURING THE SUMMER OF 19553 Station Date L I A II III IV V VI VII VIII June 20 267 . . 306 306 306 257 306 306 306 22 265 316 303 302 305 312 306 303 300 27 237 316 271 273 284 279 268 269 275 29 246 325 271 276 276 309 272 266 309 July 5 272 328 275 271 288 263 279 295 298 11 266 331 276 314 303 319 309 314 319 18 249 292 275 313 303 311 303 298 305 25 250 334 319 313 308 325 313 292 325 August 7 241 281 309 309 309 299 289 285 289 9 247 319 271 303 283 314 314 314 319 11 214 325 308 325 267 284 289 309 278 13 242 331 319 295 305 316 309 309 314 17 248 337 315 325 276 325 299 315 319 22 248 328 325 319 307 325 319 319 315 26 245 326 319 309 314 325 316 313 311 W 1 8Dates of fertilization: July 31 and August 6. 33 Figure 3. Graphic representation of the hydrogen-ion concentration. methyl orange alkalinity. and conductivity of water samples taken from the west branch of the Sturgeon River during the summer of 1955. 34 MOO. Alk' Cond. pH Mhos STATION I 280 #270 L260 i250 .240 * L230 7 5-4 \’I\ *X“\ 220 *\ f? +yx4 i' 13 4K3" 5210 I STATION A r340 8.5.. /\ P330 200'— ‘+ K - 320 * \ 8.0" +\’f~-~" I >310 190‘ “’“14‘; \-,,'.—"'“‘ ~300 k\ A .. A A 7. i x i 4'\+ ’ngx-X X qu. XVI. L290 p 280 120‘ STATION II i330 51 N/‘P/V: - 320 -..- X , ,2» 8 1‘1)— ‘~C-\-x>-..—vi—~—? T’Tbk’ \j if" - 3oo ’(\ I ¥\ 1(\ /X . 290 ”‘x " . 280 "il - J :3Jo J 1 J A4 14 A I l l l l a l I 1 1T 44 1 1 g 1 l l 1 A 3 270 10 20 30 9 19 29 0June July August Dates of Fertilization: July 31 and August 6: 1955 '——--Conductivity (Mhos X 10'6 at 18°C) " - —— Hydrogen- Ion Concentration (pH) ‘X‘-x-— Methyl Orange Alkalinity (p.p.m.) 35 Figure 3 (C ontinued) NH] STATION III I 36 Cond. os 330 320 ..310 I300 .290 £280 180h- 8.5- 170—? 8-01 -270 320 »310 +300 LZ90 i280 .270 160—4 260 1 STATION V August June Dates of Fertilization: July 31 and August 6. 1955 \———Conductivity (Mhos X 10'6 at 18°C) - ~ _—-Hydrogen-Ion Concentration (pH) ~)(~)(-— Methyl Orange Alkalinity (p.p-m.) $330 '320 '310 #300 .290 L280 i270 .260 .250 I. o 3.» L. 1‘1! '1 . .. n.;‘r\-‘ o w: . u 37 Figure 3 (Continued) 38 M.O. Alk. pH Cond. STATION VI Mhos 190 - .320 -310 180 — ~300 3.5 J —290 170 - ,’ A L280 Y ,, 8.0 1 \y”/’ \k* \*— ¥/k r270 160 —4 \/ 260 190 — STATION VII [320 ' 310 1./ ”NV“ 180 — +’/ 300 < ,1” -2 0 8.5 _ \ /}‘{t \l 9 170 -: 43’ 4r! ‘ ~V , e- - >280 8.0 v¥ 270 160 60 STATION VIII )330 x—N / /— “2" P32 0 f H- \ xm‘ _/ .310 fl 7‘\ if X\/ r300 ”"‘ ---3\7'/" ~-_,— '“' L290 . .280 [IA IL. I L [#LAAAJ n-llnlllb27o 10 20 30 9 19 29 June July August Dates of Fertilization: July 31 and August 6, 1955 \— Conductivity (Mhos X 10‘6 at 18°C) ‘ ‘ - - Hydrogen-Ion Concentration (pH) “X‘X— Methyl Orange Alkalinity (p.p.m.) 39 Biological Aufwuchs flora. For both 1954 and 1955 an obvious increase of aufwuchs flora was observed at Station I following fertilization; also. a difference was noted in the type of flora accumulated on the bricks and shingles. Strands of filamentous algae. mostly Spirogyra and Anabaena. were found on the Shingles. while the bricks were mainly encrusted with diatoms of the genera Navicula and Pinnularia. W Although there was a visible increase in quantity of aufwuchs on the bricks and shingles at Station I after fertilization. no change of this magnitude was Observed at the downstream stations. The ”null hypothesis" that no change in quantity of aufwuchs on bricks and shingles occurred, other than that attributed to sample variation, was tested by analysis of variance. The values used in this test were Obtained by subtracting the pigment density (in Harvey units) of the flora from a certain brick or Shingle before fertiliza- tion from the pigment density of the flora of a brick or shingle that was Placed in the same location after fertilization. Therefore. the resultant value is a difference from zero. being either positive or negative, depending on an increase or decrease of pigment produc- tion after fertilization. Due to the great variation in pigment pro- duction between Station I and other downstream stations. Station I 40 was excluded and stations H through VIII were considered in the analysis of variance. The 1954 results showed that there was a Similar trend in production on both the bricks and shingles after fertilization. Therefore. Grzenda (1955) pooled his data. with the results of analy- sis of variance showing a highly significant difference from zero at the 99 percent level. The mean difference from zero at each sta- tion was positive except for the bricks at Station VII. This indicated an increase in chlorophyll production at all stations except for the bricks at Station VII. Contrary to the results of 1954, a difference was observed between the mean differences from zero of the bricks and those of the shingles. Therefore. they were treated separately. Analysis of variance for the bricks showed no significant difference from zero. at the 95 percent level. after fertilization. but a significant difference at the 95 percent level between stations (Table VIII). The analysis of variance test for the shingles (Table IX) showed a highly signifi- cant difference from zero at the 99 percent level. The mean dif- ference from zero forthe shingles was a negative value. indicating a decrease in flora production as shown by the decrease in the ex- tracted pigment density. 41 TABLE VIII ANALYSIS OF VARIANCE OF CHANGES IN THE DENSITY OF CHLOROPHYLL EXTRACTED FROM AUFWUCHS ATTACHED TO THE BRICKS. EXCLUDING STATIONS I AND A W I f Source of Degorizees Sum of Mean "F" Variance Freedom Squares Squares Difference from zero . . . 1 19.5 19.5 3.30 Total .............. 31 241.3 7.78 Between stations ..... . 6 93.54 15.59 2.64* Error ........... . . . 2.5 147.8 5.91 *Significant at the 95 percent level. TABLE IX ANALYSIS OF VARIANCE OF CHANGES IN THE DENSITY OF CHLOROPHY LL EXTRACTED FROM AUFWUCHS ATTACHED TO THE SHINGLES. EXCLUDING STATIONS I AND A W Source of Degees Sum of Mean 11F” Variance Freedom Squares Squares Difference from zero . . . 1 391.5 391.5 15.66“ Total . ............ . 85 2226.0 Between stations . . . . . . 6 276.4 46.1 1.84 Error . ...... . ....... 79 I 1949-6 24-99 **High.ly significant at the 99 percent level. 1:}. 1! 42 The results of the weekly collections were not in agreement with the 30-day collections. The analysis of variance test showed a highly significant difference at the 99 percent level between weeks (Table X). The total of eight weeks were divided into four-week periods. NO significant difference was found within each of these two periods. The mean weekly values (Harvey units) were greater during the second four—week period. indicating an increase in the production of aufwuchs flora after fertilization. The statistical pro- cedure for the weekly collection was not the same as the procedure used for the 30-day collections in that the values were not ascer- tained by subtracting the pigment density of a certain brick or shingle placed in the same location the previous week. Therefore. the resultant value was not a difference from zero. The contradictory results regarding the shingles for the weekly and 30-day collections raises the question expressed by Newcombe (l949)(whi1e measuring productivity by the accumulation of attachment materials on microscope slides) on how long slides (bricks and shingles in this case) should be submerged to assure most satisfactory results. Newcombe (1949) further adds that "the time element depends a great deal on the purpose of the ex- Periment and the season of the year." The time element may be 0f prime importance in that the shingles may have a limited 43 TABLE X ANALYSIS OF VARIANCE OF CHANGES ,IN/THE DENSITY OF CHLOROPHYLL EXTRACTED FROM AUFWUCHS ATTACHED TO THE SHINGLES AT STATION IVA W Degrees Source of Sum of Mean .. .. Variance 0f Squares Squares F Freedom Total . ............ 76 617.02 Between weeks ....... 7 365.81 52.26 14.3611“!K Before vs. after fertilization . ...... 1 341.63 341.63 93.85“ Within ........... 6 24.18 4.03 1.11 Within .weeks ........ 69 251.21 3.64 ===: fl La H fire—a **Highly significant at the 99' percent level. TABLE XI ANALYSIS OF VARIANCE OF CHANGES IN THE DENSITY OF CH LOROPHY LL EXTRACTED FROM AUFWUCHS ATTACHED TO THE SHINGLES AT STATION A =3“ L - Source of Degrees Sum of Mean "F" Variance Freedom Squares Squares Total ............. 21 885.8 42.2 Between collectiOns . . . 1 72.7 72.7 2.1 Among pairs ........ 10 460.3 46.0 1.3 Error . ............ 10 352.8 35.3 44 accumulative capacity and this limit is reached within several days. Beyond this point the shingles possibly lose their efficiency in the accumulation of aufwuchs flora. either by one or a combination of the following factors: the limited carrying capacity of the shingle; loss of flora by erosion. such as molar action; or predation on the flora by aquatic fauna. Studies of the relationship between the aquatic fauna and the algal flora show that the larvae of tube dwelling chironomids. Trichoptera and Ephemeroptera. are algal feeders. and that their food consisted primarily of the filamentous diatoms and Chlorophyceae (Brook. 1955). Brook also found that a drastic reduction in the amount of algae can be correlated with the increasing efforts of the browsing fauna. The reason for these explanations is that after seven days the shingles at Station IVA accumulated nearly the same quantity of anWuchs flora as those shingles left in the stream for 30-day intervals. It is known that solar radiation and water temperature are two imporant environmental factors in the production and growth of aufwuchs flora. This was confirmed by Gumtow (1955), who found that qualitatively the floral components of the flseriphyton (aufwuchs) comp1ex remain constant but a quantitative difference was associated with environmental changes such as high water temperatures. floods. 45 and high turbidity. In comparing the first four—week period (June 3-July 30) with the second (July 30-August 27), certain environmental differences occurred. During the first four-week period there is a larger quantity of radiant energy reaching the stream and the water temperature is higher because the stream did not reach base level . w”: and its summer average minimum temperature until August. Other environmental factors appeared to remain constant; there were no signs of high turbidity or floods. Therefore. all other factors being equal. there should be greater production and growth of aufwuchs ..__, flora during the first four-week period as Shown by the 30-day col- lections. or at least no significant change illustrated by "Station A." located on the control stream (Table XI). If the weekly collections show the true trend and there is an increase in aufwuchs. then it is quite probable that the increase was due to fertilization. If we eliminate light and temperature as possi- ble causes for the increase during the second four-week period. the remaining influence appears to be the addition of nutrients. Even though phosphorus. nitrogen. and sulfates were not traced beyond Station I. there is the possibility that they reached Station IV in con- centrations that could not be detected using our chemical procedures. An explanation for the difference in taxonomic composition and results Obtained by analysis of variance between the bricks and 46 shingles is given by Ruttner (1953), who states. "The physical characteristics of the substrate to which these organisms are, at- tached are of the greatestsignificance in the formation of the Aufwuchs." It might also be added that the filamentous algae (characteristic of the shingles) would seem to be exposed more to r—— 'I i" 4 . ,r" the forces of erosion than are the diatoms encrusted on the bricks. Aufwuchs faunae. The aufwuchs fauna is comprised mostly of Amphipoda (at Station I). two families of Ephemeroptera. Tri- choptera. and Diptera. The families Hydropsychidae. Heptageniidae. Baetidae. Tendipedidae. and Simuliidae were present at all stations (see appendix). Although the sampling stations were qualitatively similar in taxonomic composition of the aufwuchs fauna. a quantitative differ- ence was observed between stations. "Studies made on the insect fauna of northern and southern Michigan trout streams since 1933 have shown that certain characteristics of bottoms. temperatures. pH and other factors. determine the numbers and kinds of insects present" (Morofsky. 1940). In that pH and temperature were rather stable during the sampling period the difference in abundance of fauna between stations appears to be the result of differences in bottom composition and stream flow. Stations V. VI. and VIII were 47 quite similar in composition and abundance; this may be correlated with the similar physical characteristics of the stream at these sta- tions. The second collection shows a noticeable increase in the per- cent of Ephemeroptera at all stations except Station I. In contrast to the Ephemeroptera. there was a decrease in the Dipterans at all ;. stations during the second collection (Figure 4). An abundance of amphipods at Station I and Brachycentridae at Station II was observed during the second collection. e.-.”— In 1954 over 95 percent of the aufwuchs fauna (consisted of Hydropsychidae and Baetidae. The family Tendipedidae must be added to include 95 percent of the fauna collected in 1955. A qualitative comparison shows that thirteen families comprised the bulk of the total collection in 1954 as compared to only seven families in 1955. A comparison of the mean number per substrate for both 1954 and 1955 (Table XII) show great variation in the abundance of organisms between stations and variation at the same stations be- tween years. There was a greater number of organisms at Station VII and VIII in 1954 than in 1955. There was also a greater abund- ance of amphipods at Station I during 1955. The mean number per substrate also shows a general trend in abundance downstream for both years. The low quantity of organisms per substrate at Station 48 Figure 4 The percentage composition of the aufwuchs fauna. _.-- Linen—p- 49 B First Collection 100? STATION A a Second Collection V . / 75 / V 50 - Fl? 1‘ 25 1. / / M 0 —£I=P~ . r—a T E D O 100L 75 - STATION I STATION II E (D 50 - g t ' tr- 0 f 0+ 1 25¢ g 0. a L T E D O 100. J 4 75 ~ 1 50 . STATION III STATION 1v ‘ 25 . 01L D O 1' . A = Amphipoda T = Trichoptera 1 D = Diptera ~ 0 2 Others { E = Ephemercmtera I __ 50 Figure 4 (Continued) 100)— 75f STATION v 501- 7" 25$ 0*. Al _ Jig—fl E T E D 0 U S-t Q) n. 100T 75; 1" STATION VII 50 - 25F ’ o. [37;] 7 f T E 51 A '2 Amphipoda D = Diptera E = Ephemeroptera E] First Collection 9 Second Collection STATION VI Us T E S TA TION ca _ T = Trichoptera O = Others RD E 1:“ D 0 e He... 0 1 W 52 TABLE XII A COMPARISON OF THE AUFWUCHS FAUNA (MEAN NUMBER PER SUBSTRATE) TAKEN FROM THE WEST BRANCH OF THE STU'RGEON RIVER DURING THE SUMMERS OF 1954 AND 1955 m First Collection Second Collection fiw *— v. Station Bricks Shingles Bricks Shingles T l 195 4 '19 55 T954 ' 1 9555 2159524 a v l 955 T9554 5 19555 I 23.0 21.8 55.0 14.4 3.7 97.6 57.2 9.5 A* . . 99.0 81.9 22.0 25.3 II 128.0 31.0 25.0 21.3 43.0 25.6 8.7 20.8 III 14.8 13.6 9.7 13.4 21.3 22.4 6.3 5.5 IV 10.2 22.4 13 .2 13.6 15.5 9.0 4.2 9.7 I V 26.2 68.0 12.8 13.1 19.0 12.8 2.5 14.9 VI 86.5 68.2 26.8 30.1 17.2 68.8 1.0 22.8 9 VII 238.7 99.8 15.8 18.9 24.3 53.2 60.2 47.5 ) VIII 233.4 106.8 161.5 44.8 38.8 72.8 25.7 35.1 *No Control Station A in 1954. 53 III is associated with the large quantity of silt which deposited on the bricks and shingles. Thus an explanation for the greater num- ber per substrate at stations VI. VII. and VIII is that the bricks and shingles at these stations were less subject to silt deposition. Bottom fauna. The bottom organisms cover a large taxonomic _.. - n. W. range. but only a few families of Insecta are of a quantitative im- portance (Table XIII). A qualitative comparison for 1954 and 1955 shows an increase in the taxonomic composition of the bottom fauna in 1955. In 1954 Baetidae. Elmidae. Brachycentridae. Tendipedidae. and the Oligochaetes made up 79 percent of all bottom organisms. Oligochaetes by themselves made up 48 percent of the total number (Grzenda. 1955). In 1955 the Oligochaetes comprised only 28 percent of the total population. Ephemeridae. Baetidae. Brachycentridae. Rhyacophilidae. Elmidae. Tendipedidae. and Oligochaetes made up approximately 90 percent of the total number of organisms. The main difference between the two years is the greater number of Ephemeridae. Rhyacophilidae. and Brachycentridae in 1955. The percent composition of the bottom fauna with regard to orders for 1955 may be seen in Table XIV. A comparison of the bottom fauna data with those obtained by Grzenda in 1954 shows a decrease in the Oligochaetes and dipterans and a substantial increase 54 TABLE XIII TAXONOMIC COMPOSITION AND ENUMERATION OF THE BOTTOM FAUNA SAMPLED FROM THE WEST BRANCH OF THE STURGEON RIVER W A: J Collection Date Taxonomic Groups June July August 24 1 8 13 20 27 12 19 25 f‘v Diptera Rhagionidae . . . . Tendipedidae . . . Simuliidae . . . . . Empididae- . . . . . Tipulidae ..... . Tabanidae . . . . . Heleidae ..... ‘ . _ Culicidae ...... . N 1oor~fowo4>m levees-Nomi» ooo~woooo~1N HQWOQD—tpw OONHHOUIN ov-toov-tho‘o OHNt-‘OHrbe {oHoi—I—afiwN l I l l l A1ooooooww p—n A N N .A yh U.) \0 N H U.) H N p Subtotals 12 Trichoptera Rhyacophilidae Brachycenttridae . Hydropsychidae Psycomyiidae . . . Leptoceridae MOlannidae Limne philidae Phryganiidae Hydroptilidae . . . Philoptamidae UT -l 17 162 121 12 .p. 00 U1 HQOU‘NOD—‘D—IWO‘ oooowsli—anxo OOHWNONubppN ooNNWOOH OOOOOOOHHN O‘I—I (Booms-Howe“) l l 1 lomomoooo { O‘ CONNOOONO‘ l l 124 H H O 0‘ \O 4 U1 \0 O Ln 0 H «I N N C CD Subtotals 39 55 TABLE XIII (Continued) W T A m Collection Date Taxonomic m H Groups June July Au gu st 24 l 8 13 20 27 12 19 25 Ephemeroptera EphemEridae '. . . 7 7 57 18 28 32 37 28 26 Baetidae ..... . 80 69 27 33 20 19 19 6 6 Heptagem‘idae . . . 12 4 1 5 5 2 0 0 0 Subtotals . . . . 99 80 85 56 53 53 56 34 32 Plecoptera Nemourfdae . . . . 0 0 0 l 0 0 I 2 1 Perlidae ..... . 0 l 0 0 0 0 0 0 0 Pteronarcidae 5 0 0 6 3 2 2 2 9 Perlodidae . . . . . 2 0 1 1 l 0 2 2 4 Subtotals 7 l 1 8' 4 2 5 6 l4 Coleoptera Elmidae . . . . . . 11 22 7 19 12 9 3 I 9 Dytiscidae . . . 0 0 0 1 0 0 0 0 0 Subtotals 11 22 7 20 12 9 3 l 9 Odonata Corduie'gasteridae 2 4 o 5 6 4 5 3 4 Gomphidae . . .. . 0 0 0 l 0 1 1 0 0 Subtotals . . . . 6 6 1 0 1 2 2 1 2 --.-'dm. 56 TABLE XIII (Continued) W m a Collection Date v——v Taxonomic ' Groups June July August 24 l 8 13 20 27 12 19 25 Oligochaeta . . . . 149 125 131 119 89 59 106 34 20 Amphipoda . . . . . 0 O 0 0 0 0 l 7 2 Gastropoda 0 l 0 1 2 0 l 0 l Pelecypoda . . . . l 1 0 0 O 2 0 0 0 Hirudinae . . . . . 0 1 10 0 0 1 0 2 0 Totals . . . . . . . . 399 332 354 338 278 214 377 308 212 r—v —v No./sq. ft. 33.3 27.7 29.5 28.2 23.2 17.8 31.2 26.3 17.7 11- 1 11! __..__ ‘-'T 11 TABLE XIV 57 COMPOSITION BY PERCENT OF THE NUIVEBER OF BOTTOM FAUNA SAMPLED FROM THE WEST BRANCH OF THE STUCRGEON RIVER FOR THE SUMMER OF 1955 Taxonomic Group Col— \ee— tion E$::- if; :22: 2:; Dip- Oligo- Oth- Date tera tera tera tera tera cheata ers 11.11133. 24 24.8 27.6 1.8 2.8 3.5 37.3 2.3 July 1 24.1 20.8 0 3 6.6 6.6 37.7 3.9 8 24.0 21.2 0 3 2.0 12.4 37.0 3.1 13 16.6 26.3 2 4 5.9 11.5 35.2 2.1 2.0 19.1 32.4 1 4 4.3 7.6 32.0 3.2 27 24.8 23.4 0 9 4.2 14.5 27.6 4.7 August 12 14.9 45.6 1 3 0.9 6.4 28.1 2.7 19 11.0 67.5 1 9 0.3 3.9 11.0 4.3 25 15.1 58.5 6.6 4 2 1.9 9.4 4.2 _ .1. v.-. 58 in Trichoptera in 1955. The increase in Trichoptera is due mainly to the greater abundance of Rhyacophilidae and Brachycentridae in 1955. The mean number per square foot per collection date ape proximates a bimodal curve for both the 1954 and 1955 collections (Figure 5). Analysis of variance tests were used to see if these differences were statistically significant. A preliminary examination of the data showed a linear relationship between the mean and the ‘E mean square for both 1954 and 1955. Because such a condition is L contrary to the basic assumption behind an analysis of variance test (Bartlett. 1947). a logarithmic transformation was used to overcome this relationship. In 1954 analysis of variance showed a significant difference among collections at the 5 percent level. The difference appeared to be caused from the variation among the Oligochaetes which comprised 48 percent of the total number of organisms (Grzenda. 1955). Therefore. Grzenda performed another analysis of variance test. omitting the Oligochaetes. the result showing no sta- tistically significant difference among collections. In 1955 the analy- sis of variance test. including. Oligochaetes (Table XV). also showed no statistically significant difference among collections. Such phe- nomenon is contrary to what one would expect from a bimodal curve. It may be that the variability is so great within collections ‘ :‘Mh;mn 59 Figure 5. A comparison of the numerical abundance of bottom fauna collected during the summers of 1954 and 1955. Mean Number per Square Foot 50_ 1954 40- l 30' l 20« 10- O 50‘ 1955 404; 30~ 20~ \‘ 4‘ V" \\\\ I, \ 10— “xxx-1.x V O “L 1_11 L J J \t"" 1 J 20 30 10 20 30 9 19 29 6 16 June July August September Collection Date Total - - - OligOchaete W— Organisms (excluding Oligochaetes) 60 6 ‘~- 9.. n-‘s I-lI-Hlu - V ,n 61 TABLE XV ANALYSIS OF VARIANCE OF NUMBERS OF BOTTOM FAUNA SAMPLES FROM THE WEST BRANCH OF THE STURGEON RIVER FOR THE SUMMER OF 1955 Source of Variance of 311111121135 SETS-n s "F" Freedom q q e .1 #5. Total ..... . ........ 1 07 12 .5945 0. 1177 Among collections ..... 8 1.0037 0.1254 1.0717 ‘3 1 I: 1 Within collections ...... 99 11.5908 0.1177 W m 62 that an analysis of variance test will not detect variation among collections. A comparison of the mean number per square foot for the two years, as shown by Figure 5, provides a graphic illustration showing that in 1955 there was a decrease in the number of Oligo- chaetes and an increase in the remaining organisms when the if “1 Oligochaetes are excluded. 5 Although the volume of bottom fauna for both years was so ‘ small that no detailed study was accomplished. the data do Show an tum. increase (approximately 14 percent) in the volume of organisms in 1955. The total volume and mean volume per square foot of bottom fauna taken at each collection in 1955 are shown in Table XVI. Surber (1951). working on a trout stream that he considered to be of "average richness." found that the average wet weights of square foot samples collected during the months of June. July. and August were 1.65. 1.18. and 1.96 respectively. Using a conversion of one cubic centimeter equaling (one gram (Ball. 1948) comparable values obtained from the west branch for June, July. and August were 0.28, 0.22, and 0.28 in 1954 (Grzenda. 1955), and 0.33, 0.33, and 0.41 in 1955, respectively. A comparison of these values with those obtained by Surber shows production to be quite low in the west branch of the Sturgeon River. 63 TABLE XVI CONDENSATION OF THE NUNIBER AND VOLUNE OF BOTTOM FAUNA SAMPLED FROM THE WEST BRANCH OF THE STURGEON RIVER FOR THE SUMNER OF 1955 Total Total Number er Volume per Collection Date Volume p Square Foot _ Number (c c ) Square Foot (C c ) June 24 ....... 399 4.0 33.3 .33 July 1 ........ 332 2.0 27.7 .17 July 8 ....... . 354 3.5 29.5 .29 July 13 ...... . 338 5.5 28.2 ' .44 July 20 . ...... 278 4.0 23.2 .33 July 27 ....... 214 5.5 17.8 .44 August 12 . . . . . 377 4.5 31.2 .36 . - u 1 .- mug—n...“ vow-'- 64 Fish samples. The results for both 1954 and 1955 (Table XVII) show that there is a longitudinal distribution of trout in the west branch of the Sturgeon River. Longitudinal succession. as de- ’ scribed by Odum (1953). is more pronounced in the first few miles of stream; also the number of individuals decreases downstream but the size of the fish increases so that the biomass density remains '- l “:1 about the same. In general. this situation was found to be true in the west branch. At Station II. approximately one mile downstream. t large numbers of small brook trout were sampled. The trout pop- ‘ ‘ ulation at this station was entirely brook trout. Samples at Station V. approximately seven miles downstream. consisted of brooks. rain- bows. and a few brown trout. Approximately eleven miles down- stream from Hoffman Lake (Station VIII) the trout population was mainly rainbows. browns (many legal-size). and a few brook trout. A comparison of the mean length per year-class for 1954 and 1955 indicates great variability within the year classes (Table XVIII). A trend can be seen towards a general increase in the mean length per year-class for the brook trout. Other than this. the variability is too great to draw any definite conclusions. Growth studies of brook trout in the north branch of the Au Sable. the Pigeon River, and Hunt Creek Show that by the middle of June the mean length per Year-class I were 6.9. 5.7. and 5.1 inches. respectively. in each 1.4 .1.) ‘1. ..‘.1.....4 . k ' os 65 TABLE XVII COMPOSITION AND ENUMERATION OF TROUT SAMPLES FROM THE WEST BRANCH OF THE STURGEON RIVER USING A DIRECT CURRENT SHOCKER W F No. Brook Trout Brown Trout Rainbow Trout Station of re - - 1- 1. 111 Fish NO. Pct. NO. Pct. No. Pct. Collected July 6. 1955 II 332 332 100.0 V 153 71 46.4 21 13.7 61 39.9 VIII 117 9 7.7 70 59.9 38 32.5 Collected August 30, 1955 II 303 303 100.0 V 225 93 41.3 11 4.9 ' 121 53.8 VIII 189 4 2.1 80 42.3 105 55.6 W m I.‘ TABLE XVIII 66 A COMPARISON OF THE NEAN LENGTH IN INCHES OF TROUT SAMPLES FROM THE WEST BRANCH OF THE STURGEON RIVER. JULY 6. 1954. AND 1955 — +— 1954 1955 H Stand- Stand- h Length of Size Length of Size Mean Mean Year Class I Brook 4.7 0.07 88 5.0 0.06 134 Brown 5.4 0.11 23 5.1 0.14 29 Rainbow 4.5 0.09 46 4.6 0.07 63 Year Class 11 Brook 6.5 0.15 48 7.6 0.20 19 Brown 8.4 0.51 7 8.2 0.24 11 Rainbow 7.2 0.16 30 6.4 0.08 9 Year Class III Brook 9.3 0.27 9 10.4 1 Brown 10.4 0.26 9 11.4 0.27 12 Rainbow . 8.2 . 2 m LE: A.. q. 1...} .~ 67 of these streams (Cooper. 1953). The mean lengths of brook trout of Year-Class I collected from the west branch in 1954 and 1955 were 4.7 and 5.0 inches respectively. Considering the Pigeon River as having average productivity and Hunt Creek to be very unproductive. the data indicate even lower productivity in the west branch of the Sturgeon River. The poor growth may be the result of the paucity of bottom fauna. The significance of the relationship between trout growth and the abundance of bottom fauna is also suggested by Allen (1951). The slight increase in the mean length per year-class found among the brook trout may be the result of the 14 percent increase in the volume of bottom fauna previously mentioned in this disserta— tion. A regression analysis (covariance analysis) following Ostle (1954) was used to test whether changes in the length-weight rela- tionship (W = an) occurred from year to year. Comparisons based on the length-weight relationship are complicated in that the rela- tionship is based on two different kinds of measurement of growth: First. the exponent n (the slope in the logarithmic form of W = an) measures the proportional increase in weight with an increase in length, and secondly. the position of the line measures the relative weight at a given length. .4111! I 111 68 Briefly. the test is a method for determining if a real differ- ence. either in slope or in position (elevation or mean value). ex- isted between the relationship for the two years (1954 and 1955) for each species of trout. A regression analysis tests. first. whether the two regression lines differ to a statistically important degree; second. if they do. whether the difference is in the slopes of the regression lines regardless of positions; and third. if there is no appreciable difference in slope. whether the difference is in position. the answers depending on the outcome of the "F" value. The results of the regression analysis for the three species of trout sampled in the west branch during the summers of 1954 and 1955 are shown in Tables XIX. XX. and XXI. Only among the rain- bow trout was there a highly significant difference in the n value (Table XXI). The difference in slope (n) of the regression lines for both years can not be explained except the slope (11 value for 1955) indicates that the older rainbows may be in better condition in 21955 (n = 3.21) than in 1954 (n = 2.90). Surber (1951) found that rainbow trout eat quantities of fila- mentous algae. which brook trout do not eat. and that rainbow trout seem to have a greater preference for aquatic forms of food than brook trout. Therefore. assuming there was an increase in bottom fauna and aufwuchs production. it is reasonable to n. I- ‘3'" TABLE XIX 69 REGRESSION (COVARIANCE) ANALYSIS OF 1n LENGTH-1n WEIGHTa RELATIONSHIP IN BROOK TROUT TAKEN FROM THE WEST BRANCH OF THE STURGEON RIVER. 1954 AND 1955 W Degrees Source of Variation of gum Of SMean Freedom quares quare Total ................... 233 111.3863 Due to general regression ..... 1 105.1240 105.1240 Deviations from general regression . . . . . ........... 232 6.2623 .0269 a. Can one regression line be used for all observations? Gain from two separate regressions over general - regression . . .............. 2 .0424 .0212 Deviations from separate regressions ............... 231 6.2199 .0269 (”F" = 1.2688; answer is yes.) W anlnl' : natural logarithm. 70 TABLE XX REGRESSION (COVARIANCE) ANALYSIS OF 1n LENGTH—1n WEIGHTa RELATIONSHIP IN BROWN TROUT TAKEN FROM THE WEST BRANCH OF THE STURGEON RIVER. 1954 AND 1955 Degrees S f M Source of Variation of sum 0 S ean Freedom quares quare Total ................... 96 109.1647 Due to general regression ..... 1 107.8941 107.8941 Deviation from general regression . . . . . . . ......... 95 1.2706 .0120 a. Can one regression line be used for all observations? Gain from two separate regressions over general regression . . . . . ........... 2 .0116 .0058 Deviations from separate regressions ............... 93 1.2590 .0135 (”F" = 2.32758; answer is yes.) 1 ====r anlnu = natural logarithm. 71 TABLE XXI REGRESSION (COVARIANCE) ANALYSIS OF 1n LENGTH—1n WEIGHTa RELATIONSHIP IN RAINBOW TROUT TAKEN FROM THE. WEST BRANCH OF THE STURGEON RIVER. 1954 AND 1955 ”—I ‘— Degrees Source of Variation of SSum 0f SMean Freedom quares quare 1 L1 1 Total . . . . . . . ......... 98 51.2815 f Due to general regression . . . . 1 50.4645 50.4645 Deviation from general regression . . . . . . ......... 97 .8170 .0084 a. Can one regression line he used for all observations? Gain from two separate regressions over general regression ............... 2 .1169 . 0584 Deviations from separate regressions ......... . . . . . 96 .7001 .0072 (”F" = 8.1111*; answer is no.) b. Can a common slope be used for the separate regression line? Deviation about lines with common slope but fitted through mean of each set of data . . . . 97 .8170 .0084 Further gains from fitting separate regressions . . _ ..... 1 .0827 .0827 Deviations about separate regressions .............. 96 .7001 .0027 (”F" = 11.486015; answer is no.) W W anln“ = natural logarithm. I"Significant at the 95 percent level. _+___ —l believe that the rainbows are most likely to benefit and would be the first to show an improvement in condition. 72 SUMMARY 1. The west branch of the Sturgeon River is located in the northern Lower Peninsula of Michigan. The watershed is in the interlobate area of the Port Huron Morainic System, an area of ex- tremely rough land unsuitable for farming due to the associated sandy soils and unfavorable slopes. 2. The physicochemical and biological characteristics of the stream indicate low productivity. The stream bottom is composed of large stretches of unproductive sand. 3. During the summer of 1955. two applications of inorganic commercial fertilizer were made to Hoffman Lake. the source of the west branch of the Sturgeon River. Following fertilization there was an increase in total and soluble phosphorus. ammonia nitrogen. and possibly. sulfates at Station I only. The alkalinity determina- tions indicate that the stream contains large quantities of calcium and magnesium carbonates. thus making the west branch an efficient buffer system. There were no changes in alkalinity. hydrogen-ion concentration. and Conductivity at the stations which could be at- tributed to fertilization. .73 74 4. Both in 1954 and 1955 there was an Obvious increase in aufwuchs flora at Station I following fertilization. Contrary to the 1954 results. in 1955 the thirty-day collections showed a decrease in flora production at the downstream stations. This is not in agreement with the results of the weekly collections where a sta- tistically significant increase was detected following fertilization. Such factors as limited carrying capacity of the shingles. erosion. predation. et cetera. may cause the shingles left in the stream for thirty-day periods to lose their efficiency in the accumulation of aufwuchs flora. This is the first year that weekly collections were obtained. From the results it is recommended that in future work the necessity of taking weekly samples be given considerable thought. 5. A comparison of the mean number per substrate of the aufwuchs fauna for both 1954 and 1955 show great variation in the abundance of organisms at the collecting stations. The variation is believed to be the result of difference in bottom type at the various stations. 6. The bottom organisms cover a large taxonomic range but only a few families are quantitatively important. There was approx- imately a 14 percent increase in the volume of organisms from 1954 to 1955. The average wet weight per square foot values show gLLn-u-v" 75 production to be low in the west branch of the Sturgeon River as compared with other similar streams. 7. There is evidence of longitudinal distribution of trout in the west branch. Starting with brook trout at the headwaters. there is a gradual displacement by rainbow and brown trout downstream. A comparison of brook trout growth in the west branch with those of f .1 other northern Michigan trout streams also indicates very low pro- ductivity in the west branch of the Sturgeon River. Results of the regression analysis for the species of trout show that only among the rainbow trout was there a highly significant difference in slope of the regression lines. indicating that the older rainbows may be in better condition in 1955. The improvement in condition may be the result of difference in food preference exhibited by the rainbows. LITERATURE CITED Alexander. Gaylord R. l 956. The fertilization of a marl lake. Michigan State University. Allen. K. Radway 1951. Master's thesis . The Horokiwi Stream- -A study of a trout population. New Zealand Marine Dept.. Fish. Bull. No. 10:231 pp American Public Health Association 1955. Standard methods for the examination of water. sew- age. and industrial wastes. ‘522 pp. 10th ed.. New York. Anton. Nickolas 1957. Biological. chemical. physical changes resulting from fertilization of a marl lake. gan State University. Master's thesis. Michi- Ball. Robert C. 1948. The relationship between available fish food. feeding habits of fish and total production in a Michigan lake. Mich. State Coll.. Ag. Exp. Sta.. Tech. Bull. 206:59 pp. Barnes. H. 1955. Chemical aspects of oceanography. tute of Chemistry; No. 4. The Royal Insti- Bartlett. M. S. 1947. The use of transformations. Brook. A. J. Biometrics, 3:39-52. 1955. The aquatic fauna as an ecological factor in studies of the occurrence of freshwater algae. Review Algolo- gique. Tome 1. No. 3, pp. 141-145. 76 77 Coffin. C. C.. F. R. Hayes. L. H. Jodrey. and S. G. Whiteway 1949. Exchange of materials in a lake as studied by the ad- dition of radioactive phosphorus. Can. Jour. Res.. D. 27:207-222. Cooper. Edwin L. 1953. Periodicity of growth and change of condition of brook trout (Salvelinus fontinalis) in three Michigan trout streams. Copeia. May 29. No. 2:107-114. Ellis. M. M., B- A. Westfall. and M. D. Ellis f l 1948. Determination of water quality. US. Dept. Inter.. f ' Fish. and Wild. Ser.. Research Rept. No. 9. r Grzenda. Alfred R. 1956. The biological response of a trout stream to headwater fertilization. Master's thesis. Michigan State University. Gumtow. Ronald B. 1955. An investigation of the periphyton in a riffle of the West Gallatin River. Montana. Trans. Am. Micros. Soc.. 124 (3):278-292. Harvey. H. W. 1934. Measurement of phytoplankton population. Jour. Mar. Bio. Assoc.. 19:761-773. Hasler. Arthur D., and Wilhelm G. Einsele 1948. Fertilization for increasing productivity of natural in- land waters. Trans. 13th N. Am. Wildl. Conference. Publ. by Wildl. Institute. Huntsman. A. G. 1948. Fertility and fertilization of streams. Jour. Fish. Res. Ed. Canada 7(5):248—253. Lagler. Karl F. 1952. Freshwater fishery biology. Wm. C. Brown Co.. Dubuque. Iowa, 360 pp. 78 Maciolek. John A. 1954. Artificial fertilization of lakes and ponds-~A review of the literature. U.S. Dept. Int.. Fish. and Wildl. Ser.. Spl. Scien. Rpt.--Fish. No. 113:41 pp. Michigan Department of Conservation 1955. Fish for more fishermen. Mich. Dept. Cons.. Lansing 26. Michigan. 48 pp. Morofsky. W. F. 1940. A comparative study of the insect food of trout. Jour. of Economic Entomolog. 33(3):544 pp. Moyle. John B. 1954. Some aspects of the chemistry of Minnesota surface waters as related to game and fish management. Inves. Rpt. No. 151. Minn. Dept. Cons., 36 pp. Neess. John C. 1949. Development and status of pond fertilization in central Europe. Trans. Am. Fish. Soc.. 1946, 76:335-358. Newcombe. Curtis L. 1950. A quantitative investigation of attachment materials in Sodon Lake. Michigan. Ecology 31(2):204-210. Odum. Eugene P. 1953. Fundamentals of ecology. W. B. Saunders Co.. Phila- delphia. Pennsylvania, 384 pp. Ostle. Bernard 1954. Statistics in research. Iowa State College Press. Ames. Iowa. 487 pp. Patrick. Ruth 1949. A proposed biological measure of stream conditions based on a survey of Conestaga Basin. Lancaster County. Pennsylvania. Pro. Acad. Nat. Sci._Phil. 101: 277-347. Rousefell. George A.. and W. H. Everhart 1953. Fishery science: its methods and applications. John Wiley and Sons. New York. 444 pp. - 1- an, _ - :_]'A.”- 79 Ruttner. Franz 1953. Fundamentals of limnology. (Translated by D. G. Frey and F. E. Fry.) Univ. Toronto Press. 242 pp. Surber. Eugene W. 1951. Bottom fauna and temperature conditions in relation to trout management in St. Mary's River, Augusta County. Virginia. Va. Jour. Sci. 2(3):190-202. Theroux. Frank R.. E. F. Eldridge. and W. L. Mallmann 1943. Laboratory manual for chemical and bacterial analysis of water and sewage. 3d ed.. McGraw-Hill. New York. 274 pp. Tucker. Allan N 1949. Pigment extraction as a method of quantitative analysis of phytoplankton. Trans. Am. Micros. Soc.. 68(1):21-23. 1956. Photo-electric- colorimetry as a method of quantitative phytoplankton analysis. Trans. Am. Micros. Soc.. 75(4);422-427. Welch. Paul S. 1952. Limnolog. McGraw-Hill. New York. 538 pp. WhiteSideu Eo Po: I- F. SChneidery and R. I. COOR 1956. Soils of Michigan. Michigan State University. Agric. Exp. Sta. Spec. Bull. 402. 52 pp. Young. 0. W. 1945. A limnological investigation of the periphyton in Douglas Lake. Michigan. Trans. Am. Micros. Soc. 64(1):1-20. APPENDIX 80 81 TAXONONIIC COMPOSITION AND ENUNIERATION OF AUFWUCHS FAUNA SAMPLED FROM THE WEST BRANCH OF THE STURGEON RIVER (Station I) W First Collection Second Collection Taxonomic Groups w +4 fi fi - 4— Bricks Shingles Bricks Shingles f —v v—v a Diptera Simuliidae ....... 0 0 0 2, Tendipedidae ..... 1 1 5 2 1 4 Rhagionidae . ..... 0 0 0 l Subtotals ...... T T5 "2— T7 Trichoptera Brachycentridae . . 0 l O 0 Hydropsychidae . . . 15 117 l 51 Psychomyiidae . . . . 0 8 O 4 Subtotals ...... T5 T56- "I 55 Ephemeroptera Baetidae . ....... 27 45 36 27 Heptageniidae ..... 0 2 3 4 Subtotals ...... E7 '47 3'9" 3'1“ Plecoptera Perlidae ........ 0 0 0 Subtotals ...... 73' "(I "'5 FT Coleoptera Elmidae . . . ..... 2 __6_ 0 __2_ Subtotals ...... 7 6 "6 2 Odonata Agrionidae . ...... 2 O O 0 Coenagrionidae . . . . 0 3 2 4 Gomphidae ....... 0 J1 J _‘l_ Subtotals ...... "'2‘ 3 2 5 Amphipoda ......... 1 9 4 444 32 Hirudinae . ........ 21 0 0 0 Gastropoda ....... . __Q_ __1_ ___(_)_ __(_)‘ Subtotals . . . . . . . . 40 5 444 32 Totals............ 37 202 488 143 Mean no./substrate . . 21 8 l4 4 97 6 93 ‘- -....__._ ____.-—- -_ -_-____ -___. -- -__#,__.——.—— 82 TAXONOMIC COMPOSITION AND ENUNIERATION OF AUFWUCHS FAUNA SAMPLED FROM THE WEST BRANCH OF THE STURGEON RIVER (Station A) m First Collection Second Collection Taxonomic Groups - - ~ - fi fl 4 Bricks Shingles Bricks Shingles Diptera Simuliidae . ..... . 2 17 45 3 l 3 Tendipedidae . . . . . 3 4 68 5 3 O Subtotals . ..... 2 5 l 52 1 "6 '33 Trichoptera . Hydropsychidae 0 2 0 2 Rhyacophilidae 7 0 O 1 Psychomyiidae . . . . 0 O O 3 Subtotals ..... . 7 2 '7)- "6- E phemeroptera Baetidae ........ 3 8 6 97 80 Z 57 Heptageniidae ..... ' 0 0 O 1 Subtotals ‘ ...... 3 8 6 97 '8? 2 58 Plecoptera Pteronarcidae 0 5 0 1 Perlodidae ..... . . 1 0 2 o Perlidae ........ 0 0 0 4 Nemouridae ...... 0 4 O 1 Subtotals ...... 1 9 2 6 Amphipoda ......... 0 0 0 1 Totals . .......... . 297 1229 88 304 .__7 Mean no./substrate . . . 99.0 81.9 22.0 25.3 83 TAXONOMIC COMPOSITION AND ENUNIERATION OF AUFWUCHS FAUNA SAMPLED FROM THE WEST BRANCH OF THE STURGEON RIVER (Station II) W First Collection Second Collection Taxonomic Groups - fl - w 44 Bricks Shingles Bricks Shingles vfi—‘ Diptera Simuliidae . ...... 5 9 3 6 0 Tendipedidae ..... 15 1 5 4 3 61 Rhagionidae ...... 0 0 O 2 Empididae ....... 0 2 0 1 Heleidae . ....... 0 0 0 3 Subtotals ...... :75- T59 ”9' '5'?— Trichoptera Brachycentridae 4 2 9 1 9 8 8 Hydropsychidae . . . 8 7 4 l 2 Psychomyiidae . . . . O 1 3 7 Limne philidae . . . 0 5 0 0 Subtotals ...... T5 T2— 36 T7 E phemeroptera E phemeridae ..... 0 7 0 0 Baetidae ........ 3 6 1 07 92 9 4 Heptageniidae ..... 0 1 0 0 Subtotals . ..... 36 TI? '92- 34 Plec optera Perlidae ........ O 1 0 0 Perlodidae ....... O 0 1 0 Nemouridae ...... 0 2 0 1 Subtotals ...... "5' .5. "5 "1— Hirudinae ......... l 0 0 0 Gastropoda ........ 0 0 0 l Oligochaeta ........ 0 0 0 1 Totals ............ 124 319 128 271 Mean no./substrate . . . 31.0 21.3 25.6 20.8 84 TAXONOMIC COMPOSITION AND ENUMERATION OF AUFWUCHS FAUNA SAMPLED FROM THE WEST BRANCH OF THE STURGEON RIVER (Station 111) Taxonomic Groups Fir st C ollection '— —v— Shingles Second Collection. fi fi Shingles Bricks Bricks Diptera Simuliidae . . . . . 4 0 14 o Tendipedidae 4 93 1 1 14 Rhagionidae...... 0 3 o o Empididae . ..... 0 1 0 0 Heleidae ........ _(_). i .2 .2 Subtotals ..... 8 9 9 2 5 1 4 Trichoptera Brachycentridae . . . 0 0 0 1 Hydropsychidae 2 0 l 0 44 12 Rhyacophilidae . . . . 0 4 0 0 Limnephilidae _0_ _2_._ "0 _2_ Subtotals ..... 2 0 1 6 44 15 Ephemeroptera Ephemeridae . . . . 0 3 0 o Baetidae ....... 37 72 38 17 Heptageniidae . . . . _1. "2. i 11. Subtotals ..... 3 8 7 7 43 4 8 Plecoptera Perlodidae ...... _1_ __0 __ A Subtotals ..... 1 0 0 0 Coleoptera Elmidae ....... _1_ _4_ __(_J‘ _9_ Subtotals ..... 1 4 0 0 Amphipoda ........ 0 5 0 5 Totals ....... .. . . . 68 201 112 82 13.6 13.4 22.4 5 5 Mean no./ substrate . . . 85 TAXONONIIC COMPOSITION AND ENUMERATION OF AUFWUCHS FAUNA SAMPLED FROM THE WEST BRANCH OF THE STURGEON RIVER (Station IV) W First Collection Second Collection Taxonomic Groups 4 4 Bricks Shingles Bricks Shingles v—v — ' ' ' Diptera Simuliidae ....... 2 3 0 o Tendipedidae ' ..... 4 74 1 23 Rhagionidae ...... 0 5 o 1 Subtotals ...... "6 82- —6 '23 Trichoptera Brachycentridae 0 l 2 1 Hydropsychidae 5 0 2 0 2 49 Rhyacophilidae . . . 1 3 0 2. Limnephilidae . . . . 0 0 0 1 Psychomyiidae . . . 0 l 1 0 Subtotals ...... 5T '25-. "5' 5'3 Ephemeroptera Baetidae ........ 48 8 5 3 8 3 6 Heptageniidae ..... 0 1 l 2 Subtotals ...... 71:8 86- .3.9- 3.8 Plecoptera Perlidae....'.... 0 2 0 o Perlodidae ....... 0 0 0 1 Pteronarcidae . . . . __0_ 0 0 3 Subtotals ...... 0 7 .5 7 Coleoptera . Elmidae ........ 7 3 0 1 Subtotals ...... ‘ —— .7 "(I "-1- Megaloptera Corydalidae ..... . 0 4 0 o Subtotals ...... "6' "'4 "6' "'6' Amphipoda ......... 0 1 0 0 Hirudinae ......... 0 0 0 1 Hydracarina . . . . . . . . 0 1 0 1 “TBtals ............ 1 12 2 04 F '7 45 126 Mean no./substrate . . . 22.4 13.6 , 9.0 9.7 86 TAXONOMIC COMPOSITION AND ENUMERATION OF AUFWUCHS FAUNA SAMPLED FROM THE WEST BRANCH OF THE STURGEON RIVER (Station IVA) W Collection Date Taxonomic Groups July August VT '_v 11 16 22 3O 9 16 20 27 Diptera Simuliidae . . . . . . 0 0 0 0 0 0 0 1 Tendipedidae 4 17 2 0 14 6 l 9 0 15 Subtotals ..... 4 17 20 14 6 19 "6 TE Trichoptera Hydropsychidae 0 0 1 0 0 0 0 0 Rhyacophilidae . . . __0 0 0 3 0 1 0 0 Subtotals . . . . . 0 0 1 3 0 1 0 0 Ephemeroptera Baetidae ....... 2 7 35 14 6 10 5 6 Heptageniidae 0 0 0 0 0 0 l 2 Subtotals ..... 2 7 3 5 14 6 10 6 8 Plecoptera , Perlidae ....... __1. __ __0 __(_1 __ 4 __1_ Subtotals . . . . . 1 0 0 4 1 Coleoptera Elmidae ....... 0 0 0 0 0 0 1 0 Subtotals . . . . . 0 0 0 1 0 O 0 l 0 Odonata Agrionidae ...... _(_)_ _(_)_ __3_ __1_ __ _0 "0- Subtotals ..... 0 0 0 3 1 0 0 Megaloptera Corydalidae ..... __0 0 0 0 __1_ _0 __1_ _0 Subtotals . . . . . 0 0 0 0 l 0 1 0 Amphipoda ........ 0 0 1 1 0 0 0 0 Gastropoda ....... 2 0 0 l 0 0 0 0 Hydracarina ....... 0 l 0 0 0 0 0 0 Totals . .......... 8 26 58 36 14 31 8 25 Mean no./substrate .. 0.8 3.3 5.8 3.6 1.6 5.2 1.1 2.8 87 TAXONOMIC COMPOSITION AND ENUNIERATION OF AUFWUCHS FAUNA SAMPLED FROM THE WEST BRANCH OF THE STURGEON RIVER (Station V) W First Collection Second Collection Taxonomic Groups s w w w (44 fi ~- ' Bricks Shingles Bricks Shingles ___ fi— Diptera Simuliidae ....... 238 0 5 1 Tendipedidae ..... 0 22 1 44 Rhagionidae ...... 0 4 0 o Empididae ‘ ....... 0 0 1 l Tipulidae ........ 0 0 0 0 Subtotals ...... 2.3.8- 3:6 “7' 71-8 Trichoptera Brachycentridae . . . 0 9 0 0 Hydropsychidae . . . 38 7 12 7 Rhyac ophilidae . . 0 8 0 14 Psychomyiidae . . . . 0 0 0 2 Limnephilidae . . . 0 0 0 l Subtotals ...... 38 2.4. T5 2.4. Ephemeroptera Baetidae ........ 6 0 85 41 1 1 8 Heptageniidae ..... _1_ 7 1 l 7 Subtotals ...... 61 '92— :: T3? Plecoptera Perlidae ........ 0 0 0 1 Pteronarcidae . . . 3 0 0 0 Perlodidae ....... 0 0 1 0 Nemouridae ...... 0 0 0 1 Subtotals ...... _3 .0. _1- "2— Amphipoda . . . . ' ..... 0 0 2 O Hirudinae . ........ 0 2 0 0 Oligochaeta ........ 0 0 0 1 Totals . . .......... . 340 144 64 208 Mean no./substrate . . . 68.0 13.1 12.8 14.9 W 88 TAXONOMIC COMPOSITION AND ENUMERATION OF AUFWUCHS FAUNA SAMPLED FROM THE WEST BRANCH OF THE STURGEON RIVER (Station VI) First Collection Second Collection Taxonomic Groups 4 L * Bricks Shingles Bricks Shingles fl Diptera Simuliidae ....... 67 1 8 94 0 Tendipedidae ..... 6 l 3 9 1 4 Rhagionidae ...... 1 3 0 2 Empididae ....... __(_1 1 0 0 Subtotals ...... 7 4 l 6 1 95 6 Trichoptera Brachyc entridae . . . 13 1 6 3 Hydropsychidae . . . 1 13 1 1 51 3 0 Psychomyiidae . . .1 . 0 1 0 2 Le ptoceridae ..... 0 _0_ _0 3 Subtotals ...... 12 6 1 3 5 7 3 8 E phemeroptera Baetidae ........ 139 228 189 285 He ptageniidae ..... 1 1 8 0 1 l Subtotals ...... 140 246 1 89 296 Plecoptera Pteronarcidae ..... 0 0 2 2 Perlodidae . ...... __(_)_ _(_1 __1_ __(_)_ Subtotals ...... 0 0 3 2 C oleoptera Elmidae ........ __ __ __0 __0 Subtotals ...... 0 0 Totals ............ 3 41 42 l . 344 3 42 Mean no./substrate . . . 68.2 30.1 68.8 22.8 89 TAXONONIIC COMPOSITION AND ENUMERATION OF AUFWUCHS FAUNA SAMPLED FROM THE WEST BRANCH OF THE STURGEON RIVER (Station VII) ___. W First Collection Second Collection Taxonomic Groups fi _4 L Bricks Shingles Bricks Shingles H7 Diptera Simuliidae . ‘ ...... 355 19 144 101 Tendipedidae ..... 4 l l 0 6 Rhagionidae ...... 1 4 1 3 Empididae ....... 0 1 0 0 Subtotals . ..... 3'66 33 T45— III)— Trichoptera Brachycentridae 9 0 0 0 Hydropsychidae 49 1 3 3 1 49 Psychomyiidae . . 2 2 2 4 Subtotals ...... F0 T5 '33 5.3 E phemeroptera ‘ Baetidae ........ 77 1 6 l 85 5 3 1 He ptageniidae ..... 2 1 1 2 15 Subtotals ...... 79 T72- 87— 5.4.6- Plecoptera Perlidae ........ 0 0 0 1 Pteronarcidae . . 0 0 1 1 Subtotals ...... "0. '75 -1_ ”2' Megaloptera C orydalidae ...... 0 5 0 1 Subtotals . ..... *0- T "0- ”1— Totals . . . . . . . . . . . . 499 227 266 712 W Mean no./substrate . 99.8 18.9 53.2 47.5 90 TAXONONIIC COMPOSITION AND ENUMERATION OF AUFWUCHS FAUNA SAMPLED FROM THE WEST BRANCH OF THE STURGEON RIVER Taxonomic Groups (Station VIII) First C ollection v E Second Collection v— w. Bricks Shingles Bricks Shingles Diptera Simuliidae ....... 462 2 62 3 04 8 0 Tendipidae ....... 7 2 1 2 if: Subtotals ...... 469 2 83 3 06 9 6 Trichoptera Brachycentridae . . . 1 0 4 2 7 Rhyacophilidae 0 0 1 8 Hydropsychidae 3 0 3 4 1 1 5 8 Le ptoc eridae ..... 0 0 0 1 Psychomyiidae "(l _(_)' "0 _2_ Subtotals ...... 40 3 8 1 4 7 6 Ephemeroptera Baetidae ........ 2 4 2 05 43 2 83 He ptageniidae _1. 1 0 __0 0 Subtotals ...... 2 5 2 1 5 43 2 83 Plecoptera Perlidae ........ 0 0 1 0 Pteronarcidae __0 _2_ _0 __0_ Subtotals ...... 0 2 1 o Gastropoda ........ 0 0 0 1 Totals ............ 534 538 364 456 Mean no./substrate . . . 106.8 44.8 72.8 35.1 W ” RT .mll'l Ll V" T” 3" R” H I III I 3 1293 03046 6019 JIHIIWIWIIIHII