Continued monitoring of fish community dynamics and abiotic factors influencing Moe Pond, summer 2006

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Continued monitoring of fish community dynamics and abiotic factors influencing, summer 26 Erika Reinicke 1 Georgette M. Walters 1 INTRODUCTION (Figure 1) is a eutrophic water body located on the Upper Site of the Biological Field Station in Otsego Country, New York. is the headwater to Willow Brook, a tributary to Otsego Lake (Albright 25). It is a 38.5 acre (15.6 ha) impoundment with an average depth of 1.8 m and is 3.8 m at the deepest point (Sohacki 1972), though in 26 the maximum depth encountered was 2.3 m. Historically, Moe Pond had a fish community consisting of golden shiners (Notemigonus crysoleucas) and brown bullhead (Ictalurus nebulosus). Golden shiners, being efficient planktivores, suppressed the abundance of zooplankton. Low algal grazing caused lower transparencies in due to algal blooms. During this time, rooted plants were absent (McCoy et al. 2). In 1999, the unauthorized stocking of largemouth bass (Micropterous salmoides) and smallmouth bass (M. dolomieui) caused trophic changes in (Lopata 24). Following the bass introduction, high piscivory on shiners caused a change in top down predation (Tibbits 2). As large bodied zooplankton rebounded, algal grazing increased and the pond became more transparent. Clearer waters allowed for the establishment of rooted plants, namely Elodea canadensis, beginning in 22. It practically covered the pond s surface in 22. As the bass forage was depleted, they turned to other food sources, including crustacean zooplankton, apparently functionally replaced the shiners as planktivores. The zooplankton population was reduced, causing an increase in phytoplankton and reduced rooted macrophyte communities (Dresser 25). Annual surveys of Moe pond were started in 1999 after the discovery of bass by Wilson et al. (2). The surveys assessed the fish (including relative abundances, diet and age structure), macrophyte and zooplankton communities. Physical and chemical water quality parameters were also assessed on a weekly basis. The purpose of this study is to continue the monitoring of tropic changes in Moe Pond. Continuing limnological and ecological surveys of will lend to better management of water quality and fish communities of small eutrophic ponds. 1 Robert C. MacWaters Internship in the Aquatic Sciences, summer 26. Present affiliation: Department of Fisheries and Wildlife Technology, SUNY Agriculture and Technical College.

Figure 1. Bathymetry of, Otsego County, NY showing the sampling location. Contours in meters (modified from Sohacki 1972). METHODS Water Quality Moe pond was monitored weekly from 5 May to 1August 26. Data were taken at the deepest point of the pond at 2.3m marked with a buoy (N 42 5.153, W 75 4.112 ). Physical data were collected using a Hydrolab Scout or a Eureka Manta. Calibration was done according to manufacturer s specifications prior to use. (Eureka 25, Hydrolab 1995). At one meter intervals from the surface to the bottom, temperature (degrees C), dissolved oxygen (mg/l), conductivity(us/cm) and ph were taken. A standard Secchi disk was used to measure transparency. Surface water samples were collected each week and were analyzed for total phosphorous (ascorbic acid method following persulfate digestion; Liao and Marten 21), total nitrogen (cadmium reduction method; Pritzlaff 23) following peroxodisulfate digestion (Ebina et al. 1983), ammonia (phenolate method; Liao 21),

and nitrate+nitrate-nitrogen (cadmium reduction method; Pritzlaff 23). All of these parameters were analyzed using a Lachat QuickChem FIA+ Water Analyzer. Chlorophyll a was also measured each week. The samples were collected in a plastic Nalgene bottle and returned to the lab. Under subdued light, samples were processed in duplicate and run through a Whatman GF/C filter, each filter having 1ml passed through. Then the filters were cut and placed in buffered acetone. The filters were ground with an electric drill to extract the chlorophyll. The amount of chlorophyll a was determined by a Turner flourometric reader (Welschmeyer 1994). Fish/Zooplankton Community Zooplankton samples were collected using a Van Dorn bottle. Five liters of water was filtered trough a 63um mesh screen, concentrated, and preserved in 7% ethanol in the lab. Volume was recorded to back calculate the number of zooplankton per liter. Three 1 ml samples were viewed in a sedgewich-rafter cell using a compound microscope. Each zooplankton found was measured, identified and recorded. The fish community of was sampled on 3 May, 5, 14 June, and 11 July, 26. A 2 ft haul seine was used to capture and collect fish. Similar methods were used in 2 and 21 were seining was used to collect fish by Tibbits (21) and Wojnar (21). In 23 and 24 Hamway (24, 25) used an electrofishing boat to collect samples due to an inability to seine because of the large standing crop of rooted macrophytes. Each seine was conducted on the south shore off the west side corner. Seines were set using a john boat. On 14 June and 11 July seines were also run on the south shore along the east side, directly above the outlet. Captured fish were measured (mm) and a scale sample was taken from fish over 15mm. Scales were taken from above the lateral line, directly behind the operculum. Scales were aged using a microprojector to determine the number of annuli. Pulsed gastric lavage, as described by Foster (1977), was used to extract stomach contents from live fish over 15mm. Stomach contents were then identified in the lab using Pecharsky (199). Largemouth bass population size was estimated through the area extrapolation method. The area seined was estimated to be 3m 2. The number of bass caught per seine was divided by the area seined. The number of fish per m 2 was then multiplied by 155,8m 2, the area of. Though this method is not considered to accurately estimate population size, it can be considered a proxy of abundance (Lopata 24), thereby allowing for relative year to year abundance estimates. Invertebrate Community Survey The invertebrate community at was surveyed on 13 July 26. The samples were taken using a semi-quantitative method at the south end and the northwest end of the Pond. The sites were chosen due to their similarity in macrophyte cover and benthic composition. Triangle nets were used to collect invertebrates. Nets were swept along the shore for 3 minutes in a 7m section. All rock and plant material was carefully

scoured. Materials and organisms collected were stored in glass collection jars and preserved in 7% ethanol. Invertebrate organisms were then identified according to Pecharsky (199). Macrophyte Community No formal marcophyte survey was conducted on Moe pond during 26. However, widespread growth of Elodea canadensis was evident. In addition, filamentous algal growing on the Elodea became prolific, starting in July. RESULLTS AND DISCUSSION Limnology limnological data from 1972 to 26 is presented in Table 1. After bass were introduced in 1999, water quality seemed to improve in that total phosphorus and cholorphyll a decreased and transparency increased (Lopata 24). However, in 24 and 25 conditions seemed to revert to what they had been prior to the bass introduction. In 26, improved water quality parameters again prevailed. Secchi Depth (m) Total phosphorus (ug/l) Nitrite+nitrate (mg/l) Chlorophyll a Alkalinity ph 1972 1994 2 21 22 23 24 25 26 NA.85 1.2 1.1 1.26 1.26 2.2 >2.2 >2.33 (.1) (.2) (.1) (.13) (.13) (.15) 4-7 36.7 26.4 29.5 42.29 56.64 26.91 NA NA (3.7) (2.6) (2.12) (2.4) (7.44) (5.49).14.11.1.1.31 NA <.5 NA NA (.2) (.2) (.1) (.6) (.4) NA 37.1 (2.2) 25.6 2.4 12. 9.76 22.94 17.3 2.53 (.2) (8.1) (2.4) (2.49) (4.4) (2.41) (19.4) 26-37 18. (.4) 17. 16. 2.1 NA NA NA (.2) (.5) (.1) 6.8-1.2 7.93 8.63 8.66 9.8 6.84 7.3 7.66 (.37) (.35) (.32) (.18) (.44) (.7) (.62) 7.3 Table 1. Summer mean values (+/- standard error) of Secchi transparency, total phosphorus, nitrite+nitrate, chlorophyll a, alkalinity and ph for, 1972, 1994 and 21-26. In 22 and 23, Secchi transparency often exceeded water depth. Fish Community Golden shiners were not collected over the study, and have not been collected since 23 (Hamway 24). Given that, it is likely that they have been extripated from. In addition, there were no smallmouth bass found in 26. This is the first year smallmouth bass have not been found in since they first appeared in 1999 (Wilson 2). Table 2 provides a summary of population estimates (+/- standard error) since monitoring began in 1994, though in 22 and 23 luxuriant Elodea growth prevented seining (Hamway 24). In those years, data represent catch per hour during electrofishing surveys

Year Golden Shiner Largemouth Bass Smallmouth Bass 1994 (McCoy et al. 2) 1999 (Wilson et al., 2) 2 (Tibbits, 21) 21 (Wojnar, 22) 7,154:+12,71;-6,356 3,21+/- 1,76 381+/- 296 1,78+/- 1,693 1,588+/- 65 2,536+/- 1,177 3,724+/-3,447 958+/- 454 945+/- 296 54+/- 473 22 (Hamway, 23) 1 23 (Hamway, 24) 1 3 2 26 318 2 1 24 (Lopata, 25) 25 (Dresser, 25) 26 (Current ) 6,924+/- 2,912 12,19+/- 3,577 11,555.17+/- 223+/- 257 Table 2. Golden shiner, largemouth bass and smallmouth bass abundances (+/- standard error), 1994, 1999-21 and 24-26. 1 Indicates years during which Elodea growth prohibited seining. Data reported as fish collected per hour of electrofishing. A summary of length vs. age is given in Figure 2. Age was estimated by viewing scales. The seined largemouth bass in summer 26 were all under 38mm and 7 years of age. The figure shows there are three dominant size distributions at young of the year, one year old and three year old fish. Length vs Age Age (years) 8 7 6 5 4 3 2 1 5 1 15 2 25 3 35 4 Length (mm) Figure 2. Largemouth bass length vs. age for, summer 26. Figure 3 summarizes the diet analysis of largemouth bass over 26, providing the mean number of each food item per stomach and the percent frequency of occurance (the percentage of bass having one or more of each food item in their stomachs). Consistent with most recent years, dipterans were the most common taxon consumed. However, the second most prevalent taxon found was amphipoda, whereas odonatates has been predominant in previous year (Lopata 24). Daphnia numbers per stomach, while common, have continued to decrease, as they have since 24.

Taxa Mean per stomach % Occurrence Largemouth Bass Acariformes.1 7.14 Copepod.9 7.14 Amphipoda 3.44 42.86 Ephemeroptera.7 8.57 Odanata 1.43 32.86 Hemipetra.7 7.14 Coleoptera 1.77 25.71 Daphnia 1.81 25.71 Diptera 5.8 68.57 Decapoda.7 7.14 Arachnid.1 8.57 Ostracod.23 4.29 Mollusca.7 5.71 Ictaluria nebulosus 2.86 8.57 Table 3. Stomach contents, including mean number of items per stomach and percent occurrence of each, of largemouth bass collected in, summer 26. Invertebrate Community Invertebrates collected and documented in 26 (Table 4) were found to be significantly less then in previous years (Lopata 24). South End North End Taxa # Collected Taxa # Collected Hirudinea 2 Hirudinea 12 Planorbidae (Rams Horn Snails) Planorbidae (Rams Horn Snails) 1 Valvatidae (Valve Snails) 7 Valvatidae (Valve Snails) 2 Sphaeriidae (Finger Nail Clams) Sphaeriidae (Finger Nail Clams) 1 Amphipoda (Scuds) 6 Amphipoda (Scuds) 36 Acariformes (Water Mites) 2 Acariformes (Water Mites) 2 Ephemeroptera (Mayflies) 1 Ephemeroptera (Mayflies) 8 Trichoptera (Cadisflies) 4 Trichoptera (Cadisflies) 12 Hemiptera 7 Hemiptera 4 Anisoptera (Dragonflies) 1 Anisoptera (Dragonflies) 2 Zygoptera (Damsleflies) Zygoptera (Damsleflies) 4 Coleoptera (Beetles) 13 Coleoptera (Beetles) 9 Diptera (True Flies) Diptera (True Flies) TOTAL 43 TOTAL 111 Table 4. Invertebrate collected at, summer 26.

The lack of invertebrates could be attributed to the large bass population present in. The rocky shore where the inverts were collected may have actually hindered collection as there may be more invertebrates using plants as cover (Dresser 25, Lopata 24). Consistent with 25 results, there were more species collected at the northern end of the pond. Also, similar to 24 and 25, the most abundant organisms found were amphipods and snails (Lopata 24, Dresser 25). Zooplankton Community The mean abundance of zooplankton and their s, by taxa, for the summers of 25 and 26, are provided in Table 5. Mean abundances and lengths for each sampling period id given in Table 6. Densities were found to be significantly lower in 26 then in recent years. It seems as though as the bass ate other available forage, they turned to alternative food sources, including large bodied zooplankton. The high chlorophyll a concentrations also indicate suppressed filtering rates. Summer 25 Summer 26 Bosmina longirostris 32 34 Bosmina longirostris 3 36 Daphnia pulex 15 81 Daphnia pulex 2 24 Cylopoid sp. 43 541 Calanoid 1 497 Calanoid sp. 8 466 Cylopoid sp. 13 446 Nauplius sp. 26 218 Nauplius sp. 37 171 Kellicotia longispina 1 185 priodontus 7 353 Keratella cochlearis 321 13 Kellicotia longispina 7 134 Ostracoda 8 577 Keratella cochlearis 22 19 Unknown 17 139 Polyartha vulgaris 234 Mean Total /L: 48 Mean Total/L: 92 Table 5. Zooplankton abundances and in, summer and 25 26.

5/25/26 6/1/26 Bosmina longirostris Bosmina longirostris 1 182 Daphnia pulex Daphnia pulex Calanoid Calanoid Cylopoid sp. Cylopoid sp. 16 614 Nauplius sp. 4 154 Nauplius sp. 27 178 priodontus 23 116 priodontus 7 391 Kellicotia longispina 17 124 Kellicotia longispina 3 139 Keratella cochlearis 13 111 Keratella cochlearis 33 11 Polyartha vulgaris Polyartha vulgaris Mean Total/L: Mean Total/L: 6/7/26 6/14/26 Bosmina longirostris Bosmina longirostris 3 79 Daphnia pulex Daphnia pulex Calanoid Calanoid Cylopoid sp. 17 515 Cylopoid sp. Nauplius sp. 1 122 Nauplius sp. priodontus 3 712 priodontus Kellicotia longispina 3 118 Kellicotia longispina 17 156 Keratella cochlearis 13 9 Keratella cochlearis 3 82 Polyartha vulgaris 3 234 Polyartha vulgaris Mean Total/L: 49 Mean Total/L: 5 Table 6. Zooplankton abundance and by week, summer 26.

6/27/26 7/5/26 Bosmina longirostris 7 157 Bosmina longirostris Daphnia pulex Daphnia pulex Calanoid Calanoid 7 497 Cylopoid sp. 7 539 Cylopoid sp. 4 257 Nauplius sp. 93 148 Nauplius sp. 7 248 priodontus priodontus 2 242 Kellicotia longispina Kellicotia longispina Keratella cochlearis 3 89 Keratella cochlearis 47 181 Polyartha vulgaris Polyartha vulgaris Mean Total/L: 137 Mean Total/L: 121 7/11/26 7/18/26 Bosmina longirostris Bosmina longirostris Daphnia pulex Daphnia pulex 3 24 Calanoid Calanoid Cylopoid sp. 3 42 Cylopoid sp. 2 339 Nauplius sp. 43 174 Nauplius sp. 47 19 priodontus priodontus 7 198 Kellicotia longispina Kellicotia longispina Keratella cochlearis 2 147 Keratella cochlearis 17 91 Polyartha vulgaris Polyartha vulgaris Mean Total/L: 93 Mean Total/L: 94 Table 6 (cont.). Zooplankton abundance and by week, summer 26.

7/24/26 8/1/26 Bosmina longirostris Bosmina longirostris 7 12 Daphnia pulex 1 32 Daphnia pulex 3 87 Calanoid Calanoid Cylopoid sp. Cylopoid sp. 3 438 Nauplius sp. 73 174 Nauplius sp. 3 148 priodontus 3 459 priodontus Kellicotia longispina Kellicotia longispina Keratella cochlearis 2 92 Keratella cochlearis Polyartha vulgaris Polyartha vulgaris Mean Total/L: 16 Mean Total/L: 43 Table 6 (cont.). Zooplankton abundance and by week, summer 26. REFERENCES Albright, M.F. 25. Changes in water quality in an urban stream following the use of organically derived deicing products. Lake and Reserv. Management. 21(1): 119-124. Albright, M.F., W.N. Harman, W.T. Tibbits, M.S. Gray, D.M. Warner and R.J. Hamway. 24. Biomanifulation: A classic example in a shallow eutrohic pond. Lake and Reserv. Manage. 2(3):181-187. Eureka Environmental Engineering. Amphibian User s Guide. Eureka Manta TM 25. Austin, TX. Foster, J.R. 1977. Pulsed gastric lavage: An efficient method of removing the stomach contents of live fish. Prog. Fish Culturist 39(4): 166-169. Hamway, R.J. 23. Continued monitoring of after the unauthorized stocking of smallmouth and largemouth bass. In 35 th Ann. Rept. (22). SUNY Oneonta Bio. Fld. Sta., SUNY Oneonta.

Hamway, R.J. 24. Continued monitoring of after the unauthorized stocking of smallmouth and largemouth bass. In 36 th Ann. Rept. (23). SUNY Oneonta Bio. Fld. Sta., SUNY Oneonta. Harman, W.N. 1972. Aquatic biology studies. In 4 th Ann. Rept. (1971). SUNY Oneonta Bio. Fld. Sta., SUNY Oneonta. Hydrolab Corp. 1995. Scout TM operating manual. Hydrolab Corp. Austin, TX. Lopata, 25. Fifth annual report on the status of following the stocking of Micropterous salmaoides and M. dolomieui. In 37 th Ann. Rept. (24). SUNY Oneonta Bio. Fld. Sta.,SUNY Oneonta. McCoy, M.C.P., C.P. Madenjian, J.V. Adams, W.N. Harman, D.W. Warner, M.F. Albright and L.P. Sohacki. 2. limnology ad fish population biology: an ecosystem approach. 33ed Occasional Paper. SUNY Oneonta Bio. Fld. Sta., SUNY Oneonta. Pecharsky, B.L., P.R. Fraissinet, M.A. Penton and D.J. Conklin 199. Freshwater macroinvertebrates of northeastern Norht America. Cornell University Press, Ithaca. Sohacki, L.P. 1972. Limnologyical studies on. In 5 th Ann. Rept. SUNY Oneonta Bio. Fld. Sta., SUNY Oneonta. Tibbits, W.T. 21. Consequences and management strategies concerning the unauthorized stocking of smallmouth bass and largemouth bass in. In 33ed Ann. Rept. (2) SUNY Oneonta Bio. Fld. Sta., SUNY Oneonta. Welschmeyer, N.A. 1994. Fluorometric analysis of chlorophyll a in the presence of chlorolphyll and pigments. Limnol. And Oceanogr. 39: 1985-1992. Wilson, B. J. D.M.Warner and M.S.Gray. 2. An evaluation of Moe ond following the authorized stocking of smallmouth and largemouth bass. In 32ed Ann. Rept. (1999). ) SUNY Oneonta Bio. Fld. Sta., SUNY Oneonta. Wojnar, K.A. 22. The continuing evaluation of after the unauthorized stocking of smallmouth and largemouth bass. In 34 th Ann. Rept. (21). ) SUNY Oneonta Bio. Fld. Sta., SUNY Oneonta.