Hostname: page-component-cd9895bd7-fscjk Total loading time: 0 Render date: 2024-12-24T18:03:55.399Z Has data issue: false hasContentIssue false

Comparisons between experimentally- and atmospherically-acidified lakes during stress and recovery

Published online by Cambridge University Press:  05 December 2011

D. W. Schindler
Affiliation:
Departments of Zoology and Botany, University of Alberta, Edmonton, Alberta T6G 2E9, Canada
T. M. Frost
Affiliation:
Trout Lake Station, Center for Limnology, University of Wisconsin, Madison, WI, 53706, U.S.A.
K. H. Mills
Affiliation:
Freshwater Institute, Fisheries and Oceans Canada, 501 University Crescent, Winnipeg, Manitoba R3T 2N6, Canada
P. S. S. Chang
Affiliation:
Freshwater Institute, Fisheries and Oceans Canada, 501 University Crescent, Winnipeg, Manitoba R3T 2N6, Canada
I. J. Davies
Affiliation:
Freshwater Institute, Fisheries and Oceans Canada, 501 University Crescent, Winnipeg, Manitoba R3T 2N6, Canada
L. Findlay
Affiliation:
Freshwater Institute, Fisheries and Oceans Canada, 501 University Crescent, Winnipeg, Manitoba R3T 2N6, Canada
D. F. Malley
Affiliation:
Freshwater Institute, Fisheries and Oceans Canada, 501 University Crescent, Winnipeg, Manitoba R3T 2N6, Canada
J. A. Shearer
Affiliation:
Freshwater Institute, Fisheries and Oceans Canada, 501 University Crescent, Winnipeg, Manitoba R3T 2N6, Canada
M. A. Turner
Affiliation:
Freshwater Institute, Fisheries and Oceans Canada, 501 University Crescent, Winnipeg, Manitoba R3T 2N6, Canada
P. J. Garrison
Affiliation:
Wisconsin Department of Natural Resources, 3911 Fish Hatchery Road, Fitchburg, WI, 54880, U.S.A.
C. J. Watras
Affiliation:
Wisconsin Department of Natural Resources, 3911 Fish Hatchery Road, Fitchburg, WI, 54880, U.S.A.
K. Webster
Affiliation:
Wisconsin Department of Natural Resources, 3911 Fish Hatchery Road, Fitchburg, WI, 54880, U.S.A.
J. M. Gunn
Affiliation:
Ontario Ministry of Natural Resources and Department of Biology, Laurentian University, Sudbury, Ontario P3E 5P9, Canada
P. L. Brezonik
Affiliation:
Department of Civil and Mineral Engineering, University of Minnesota, Minneapolis, MN, 55455, U.S.A.
W. A. Swenson
Affiliation:
Center for Lake Superior Environmental Studies, University of Wisconsin, Superior, WI, 54880, U.S.A.
Get access

Synopsis

In experiments lakes 223 (L223) and 302 South (L302S) in the Experimental Lakes Area in north-western Ontario, and Little Rock Lake (LRL) in northern Wisconsin, were progressively acidified with sulphuric acid from original pH values of 6.1–6.8 to 4.7–5.1. Although the lakes were at different locations with different physical settings and assemblages of plants and animals including fish, there were remarkable similarities in their responses, particularly in regard to biogeochemical processes and effects on biota at lower trophic levels.

All three lakes generated an important part of their buffering capacity internally b\ the reduction of sulphate, and to a lesser extent by the reduction of nitrate. Alkalinity production increased as concentrations of biologically-active strong acid anions increased. Models relating the residence times of sulphate and nitrate to water renewal, or first-order kinetics, effectively predicted events.

Acidification disrupted nitrogen cycling in all three lakes. Nitrification was inhibited in L223 and L302S, while in LRL, nitrogen fixation was greatly decreased at low pH.

The phytoplankton communities of all three lakes were originally dominated by chrysophyceans and cryptophyceans. However acidification changed the dominant species and decreased diversity. Acidification tended to increase phytoplankton production and standing crop slightly, probably because light penetration was increased.

Littoral zones of all three lakes became increasingly dominated by a few species of filamentous green algae, which created nuisance blooms by pH 5.6. Mats or clouds of algae changed the entire character of the littoral zone.

Acidification of L223 and L302S caused the loss of several species of large benthic crustaceans as pH changed from 6 to 5.6. Large, acid-sensitive littoral crustaceans were absent from LRL before acidification, probably because the lake was already too acidic.

As acidity increased, the dominance of cladocerans within zooplankton communities increased. Daphnia catawba appeared at pH values near 5.6 and became more abundant at lower pHs as the lakes were acidified. Its appearance coincided with a decline in other Daphnia species: another cladoceran, Bosmina longirostris, increased in the experimentally-acidified lakes as did Keratella taurocephala: they became the dominant rotifers. Several sensitive zooplankton species declined or disappeared as the lakes were acidified, most notably Daphnia galeata mendotae, Epischura lacustris, Diaptomus sicilis and Keratella cochlearis.

The responses of different fish varied; they appeared to depend on the sensitivity of key organisms in the food chain. The ability of key fish species to reproduce was impaired as early as pH 5.8; their reproduction, except for yellow perch in LRL, had ceased at pH 5.0 in all the three lakes.

Acidification consistently reduced the diversity and richness of species in taxonomic groups studied, these effects resulting from losses of species and the increased dominance of a few acidophilic taxa.

Responses of experimentally-acidified lakes in north-western Ontario and atmospherically-acidified lakes in eastern Ontario were similar in most respects where records allowed comparisons to be made, notably in relation to biogeochemical processes and the disappearance of acid-sensitive biota.

When the acidification of L223 was reversed, several biotic components recovered quickly. Fish resumed reproduction at pHs similar to those at which it ceased when the lake was being acidified. The condition of lake trout improved as a result of greatly increased populations of small fish, their prey. Many species of insects and crustaceans that had been extirpated by acidification returned. Assemblages of phytoplankton and chironomids have retained an acidophilic character, although their diversity during recovery is similar to that at comparable pHs during progressive acidification. As their chemistry recovered, atmospherically-acidified lakes in the Sudbury area were able to sustain recruitment by species offish, including lake trout and white sucker, with rapid increases in the diversity of invertebrate taxa. Results from both L223 and lakes near Sudbury suggest a rapid partial recovery of lacustrine communities when acidification is reversed.

It is concluded that the experimental lakes responded similarly to acidification, and that experimental acidification can reliably indicate the effects of acidification attributable to acidic precipitation.

Type
Research Article
Copyright
Copyright © Royal Society of Edinburgh 1990

Access options

Get access to the full version of this content by using one of the access options below. (Log in options will check for institutional or personal access. Content may require purchase if you do not have access.)

References

Almer, B., Eckstrom, W. & Hornstrom, E. 1974. Effects of acidification on Swedish lakes. Ambio 3, 30–6.Google Scholar
Amaral, J. A., Hesslein, R. H., Rudd, J. W. M. & Fox, D. E. 1989. Loss of total sulfur and changes in sulfur isotope ratios due to drying of lacustrine sediments. Limnology and Oceanography 34, 1351–8.CrossRefGoogle Scholar
Baker, L. A. & Brezonik, P. L. 1988. Dynamic model of internal alkalinity generation: calibration and application to precipitation-dominated lakes. Water Resource Research 24, 6574.CrossRefGoogle Scholar
Baker, L. A. & Pollman, C. D. 1986. Model of internal alkalinity generation: sulfate retention component. Water, Air and Soil Pollution 31, 8994.CrossRefGoogle Scholar
Baker, L. A. & Urban, N. 1989. The biogeochemistry of sulfur in a dilute, acidic seepage lake, pp. 79100. In Biogenic Sulfur in the Environment, eds, Saltzman, E. S. & Cooper, W. J. ACS Symp. Ser. 393. Washington, D.C.: American Chemical Society.CrossRefGoogle Scholar
Battarbee, R. W., Flower, R. J., Stevenson, A. C., Jones, V. J., Harriman, R. & Appleby, P. G. 1988. Diatom and chemical evidence for reversibility of acidification in Scottish lochs. Nature 332, 530–2.CrossRefGoogle Scholar
Beggs, G. L. & Gunn, J. M. 1986. Response of lake trout (Salvelinus namaycush) and brook trout (S. fontinalis) to surface water acidification in Ontario. Water, Air and Soil Pollution 30, 711–17.CrossRefGoogle Scholar
Berrill, M., Hollett, L., Margosian, A. & Hudson, J. 1985. Variation in tolerance to low environmental pH by the crayfish Orconectes rusticus, O. propinquus, and Cambarus robustus. Canadian Journal of Zoology 63, 2586–9.CrossRefGoogle Scholar
Bilyj, B. & Davies, I. J. 1989. Descriptions and ecological notes on seven new species of Cladotanytarsus (Chironomidae: Diptera) collected from an experimentally acidified lake. Canadian Journal of Zoology 67, 948–62.CrossRefGoogle Scholar
Bleiwas, A. S. H.. Stokes, P. M. & Olaveson, M. M. 1984. Six years of plankton studies in the LaCloche region of Ontario. Verhandlungen Internationale Vereinigung für Limnologie 22, 332–7.Google Scholar
Brezonik, P. L., Baker, L. A., Eaton, J., Frost, T., Garrison, P., Kratz, T., Magnuson, J., Perry, J., Rose, W., Shepherd, B., Swenson, W., Watras, C. & Webster, K. 1985. Experimental acidification of Little Rock Lake, Wisconsin: Baseline studies and predictions of lake responses to acidification. Special Research Report #7. University of Minnesota, St Paul: Water Resources Research Center.CrossRefGoogle Scholar
Brezonik, P. L. 1986. Experimental acidification of Little Rock Lake, Wisconsin. Water, Air and Soil Pollution 31, 115–21.CrossRefGoogle Scholar
Brezonik, P. L., Baker, L. A. & Perry, T. E. 1987. Mechanisms of alkalinity generation in acid-sensitive softwater lakes. In Chemistry of Aquatic Pollutants, pp. 229–60, eds, Hites, R. & Eisenreich, S. J. Adv. Chem. Ser. 216. Washington, D.C.: American Chemical Society.Google Scholar
Brezonik, P. L., Mach, C. E., Downing, G., Richardson, N. & Brigham, M. 1990. Effects of acidification on minor and trace metal chemistry on Little Rock Lake, Wisconsin. Environmental Toxicology and Chemistry 9, 871–85.CrossRefGoogle Scholar
Brezonik, P. L., Sampson, C. J. & Weir, E. P. 1991. Effects of acidification on chemical composition and chemical cycles in a seepage lake: mechanistic inferences from a whole-lake experiment. Preprint Ext. Abs., Div. Environ. Chem., Nat'l. Meet., Amer. Chem. Soc., April 14–19, Atlanta, Georgia.Google Scholar
Carpenter, S. R. 1989. Replication and treatment strength in whole-lake experiments. Ecology 70, 453–63.CrossRefGoogle Scholar
Carpenter, S. R. 1990. Large-scale perturbations: opportunities for innovation. Ecology 71, 2038–43.CrossRefGoogle Scholar
Carpenter, S. R., Kitchell, J. F., Hodgson, J. R., Cochran, P. A., Elser, J. J., Elser, M. M., Lodge, D. M., Kretchmer, D., HE, X. & von Ende, C. N. 1987. Regulation of lake primary production by food web structure. Ecology 68, 1863–76.CrossRefGoogle ScholarPubMed
Carpenter, S. R., Frost, T. M., Heisey, D. & Kratz, T. K., 1989. Randomized intervention analysis and the interpretation of whole ecosystem experiments. Ecology 70, 1142–52.CrossRefGoogle Scholar
Chang, P. S. S. & Malley, D. F. 1989. Partial recovery of the zooplankton community in a small Precambrian Shield lake as experimental acidification is reduced. Symp. Biol. Hung. 38, 203–8.Google Scholar
Charles, D. F., Battarbee, R. W., Renberg, I., Van Dam, H. & Smol, J. P., 1990. Paleoecological analyses of lake acidification trends in North America and Europe using diatoms and chrysophytes. In Acid Precipitation: Soils, Aquatic Processes and Lake Acidification, pp. 207–76, eds, Norton, S. A., Lindberg, S. E. & Page, A. L. New York: Springer-Verlag.CrossRefGoogle Scholar
Cook, R. B. & Schindler, D. W. 1983. The biogeochemistry of sulfur in an experimentally acidified lake. Ecology Bulletin 35, 115–27.Google Scholar
Cook, R. B., Kelly, C. A., Schindler, D. W. & Turner, M. A. 1986. Mechanisms of hydrogen ion neutralization in an experimentally acidified lake. Limnology and Oceanography 31, 134–48.CrossRefGoogle Scholar
Davies, I. J. 1989. Population collapse of the crayfish Orconectes virilis in response to experimental whole-lake acidification. Canadian Journal of Fisheries and Aquatic Sciences 46, 910–22.CrossRefGoogle Scholar
Detenbeck, N. E. & Brezonik, P. L. 1991. Phosphorus sorption by sediments in a soft-water seepage lake. 1. An evaluation of kinetic and equilibrium models. Environmental Science and Technology 25, 395403.CrossRefGoogle Scholar
Detenbeck, N. E., 1991. Phosphorus sorption by sediments in a soft-water seepage lake. 2. Effects of pH and sediment composition, Environmental Science and Technology 25, 403–9.CrossRefGoogle Scholar
Dillon, P. J., Reid, R. A. & Girard, R. 1986. Changes in the chemistry of lakes near Sudbury, Ontario following reduction of SO2 emission. Water, Air and Soil Pollution 31, 5965.CrossRefGoogle Scholar
Dillon, P. J., Yan, N. D. & Harvey, H. H. 1984. Acidic deposition: effects on aquatic ecosystems. CRC Critical Review of Environmental Contamination 13, 167–94.CrossRefGoogle Scholar
Dixit, S. S., Dixit, A. S. & Evans, R. D. 1987. Paleolimnological evidence of recent acidification in two Sudbury (Canada) lakes. Science of the Total Environment 67, 5367.CrossRefGoogle Scholar
Dixit, S. S., Dixit, A. S. & Smol, J. P. 1991. Algal microfossils provide high temporal resolution of environmental change. Environmental Science and Technology (in press).Google Scholar
Findlay, D. L. & Kasian, S. E. M. 1986. Phytoplankton responses to acidification of Lake 223, Experimental Lakes Area, northwestern Ontario. Water, Air and Soil Pollution 30, 719–26.CrossRefGoogle Scholar
Findlay, D. L. 1990. Phytoplankton communities of lakes experimentally acidified with sulfuric and nitric acids. Canadian Journal of Fisheries and Aquatic Sciences 47, 1378–86.CrossRefGoogle Scholar
Findlay, D. L. 1991. Response of a phytoplankton community to controlled partial recovery from experimental acidification. Canadian Journal of Fisheries and Aquatic Sciences (in press).CrossRefGoogle Scholar
Forsberg, C., Moring, G. & Wetzel, R. G. 1985. Indications of the capacity for rapid reversibility of lake acidification. Ambio 14, 164–6.Google Scholar
France, R. L. 1987. Reproductive impairment of the crayfish Orconectes virilis in response to acidification of Lake 223. Canadian Journal of Fisheries and Aquatic Science 449 (Suppl. 1), 107–13.CrossRefGoogle Scholar
France, R. L. & Graham, L. 1985. Increased microsporidian parasitism of the crayfish Orconectes virilis in an experimentally acidified lake. Water, Air and Soil Pollution 26, 129–36.CrossRefGoogle Scholar
Frost, T. M. & Montz, P. K. 1988. Early zooplankton response to experimental acidification in Little Rock Lake, Wisconsin, USA. Verhandlungen Internationale Vereinigung für Limnologie 23, 2279–85.Google Scholar
Geelen, J. F. M. & Leuven, R. S. E. W. 1986. Impact of acidification on phytoplankton and zooplankton communities. Experimentia 42, 486–94.CrossRefGoogle Scholar
Gonzalez, M. J., Frost, T. M. & Montz, P. K. 1990. Effects of experimental acidification on rotifer population dynamics in Little Rock Lake, Wisconsin, U.S.A. Verhandlungen Internationale Vereinigung für Limnologie 24, 449–56.Google Scholar
Graham, R. W. & Turner, M. A. 1987. Photoinhibition of respiration in epilithic periphyton. Canadian Journal of Fisheries and Aquatic Sciences 44 (Suppl. 1), 150–3.CrossRefGoogle Scholar
Grapentine, L. C. 1987. Consequences of environmental acidification to the freshwater amphipod Hyalella azteca. M.Sc. thesis. U. of Manitoba, Winnipeg.Google Scholar
Gunn, J. M. & Keller, W. 1990. Biological recovery in an acid lake after reductions in industrial emissions of sulfur. Nature 345, 431–3.CrossRefGoogle Scholar
Gunn, J. M., McMurty, M. J., Castleman, J. M., Keller, W. & Powell, M. J. 1988. Changes in the fish community of a limed lake near Sudbury, Ontario: effects of chemical neutralization or reduced atmospheric deposition of acids. Water, Air & Soil Pollution 41, 113–36.CrossRefGoogle Scholar
Hall, R. J. & Ide, F. P. 1987. Evidence of acidification effects on stream insect communities in central Ontario between 1937 and 1985. Canadian Journal of Fisheries and Aquatic Sciences 44, 1652–7.CrossRefGoogle Scholar
Hamilton, A. L. 1971. Zoobenthos of fifteen lakes in the Experimental Lakes Area, northwestern Ontario. Journal of the Fisheries Research Board of Canada 28, 257–63.CrossRefGoogle Scholar
Harvey, H. H. 1980. Widespread and diverse changes in the biota of North American lakes and rivers coincident with acidification. In Ecological Impact of Acid Precipitation, pp. 93–8, eds, Drablos, D. & Tollan, A. Oslo, Norway: SNSF Project.Google Scholar
Howell, E. T. & Stokes, P. M. 1990. The usefulness of periphyton to detect acidification of freshwaters. (In preparation)Google Scholar
Howell, E. T., Turner, M. A., France, R. L., Jackson, M. B. & Stokes, P. 1990. Comparison of Zygnematacean (Chlorophyta) algae in the metaphyton of two acidic lakes. Canadian Journal of Fisheries and Aquatic Sciences 47, 1085–92.CrossRefGoogle Scholar
Howell, E. T., Turner, M. A., Adare, K. & Sigurdson, L. 1991. Patterns of growth of Zygogonium tunetanum, a nuisance alga proliferating in the littoral zone of acidic lakes in Ontario, Canada. (In preparation)Google Scholar
Hultberg, H. & Andersson, I. 1982. Liming of acidified lakes: induced long-term changes. Water, Air and Soil Pollution 18, 311–31.CrossRefGoogle Scholar
Hurlbert, S. H. 1984. Pseudoreplication and the design of ecological field experiments. Ecological Monographs 54, 187211.CrossRefGoogle Scholar
Hurley, J. P. & Watras, C. J. 1991. Identification of bacteriochlorophylls in lakewater via reverse phase HPLC. Limnology and Oceanography (in press).CrossRefGoogle Scholar
Hutchinson, T. C. & Havas, M. 1986. Recovery of previously acidified lakes near Coniston, Canada following reductions in atmospheric sulfur and metal emissions. Water, Air and Soil Pollution 28, 319–33.CrossRefGoogle Scholar
Jackson, M. B., Vandermeer, E. M., Lester, N., Booth, J. A., Molot, L. & Gray, I. M. 1990. Effects of neutralization and early reacidification on filamentous algae and macrophytes in Bowland Lake. Canadian Journal of Fisheries and Aquatic Sciences 47, 432–9.CrossRefGoogle Scholar
Keller, W. & Pitblado, J. R. 1986. Water quality changes in Sudbury area lakes: A comparison of synoptic surveys in 1974–1976, and 1981–1983. Water, Air and Soil Pollution 29, 285–96.CrossRefGoogle Scholar
Keller, W., Gunn, J. M. & Yan, N. D. 1991. Evidence of biological recovery of acid-stressed lakes near Sudbury, Canada. Environmental Pollution (in press).CrossRefGoogle Scholar
Kelly, C. A. & Rudd, J. W. M. 1991. Site-to-site variation in the formation and accumulation of inorganic and organic sulfur compounds in lake sediments. Limnology and Oceanography (in press).Google Scholar
Keller, W., Rudd, J. W. M., Hesslein, R. H., Schindler, D. W., Dillon, P. J., Driscoll, C., Gherini, S. A. & Hecky, R. E. 1987. Prediction of biological acid neutralization in acid-sensitive lakes. Biogeochemistry 3, 129–40.Google Scholar
Keller, W., Rudd, J. W. M. & Schindler, D. W. 1990. Lake acidification by nitric acid: future considerations. Water, Air and Soil Pollution 50, 4961.Google Scholar
Kelso, J. R. M. & Jeffries, D. S. 1988. Response of headwater lakes to varying atmospheric deposition in north-central Ontario. Canadian Journal of Fisheries and Aquatic Sciences 45, 1905–11.CrossRefGoogle Scholar
Kenoyer, G. J. 1986. Groundwater/lake dynamics and chemical evolution in a sandy silicate aquifer in northern Wisconsin. Ph. D. thesis, University of Wisconsin, Madison.Google Scholar
Kettle, W. D., Moffett, M. F. & DeNoyelles, F. Jr, 1987. Vertical distribution of zooplankton in an experimentally acidified lake containing a metalimnetic phytoplankton peak. Canadian Journal of Fisheries and Aquatic Sciences 44 (Suppl. 1), 91–5.CrossRefGoogle Scholar
King, S. O., Mach, C. E. & Brezonik, P. L. 1991. Changes in trace metal concentrations in lake water and the biota from experimentally acidified Little Rock Lake, Wisconsin. Environmental Pollution(in press).CrossRefGoogle Scholar
Kratz, T. K., Magnuson, J. J., Bowser, C. J. & Frost, T. M. 1986. Rationale for data collection and interpretation in the Northern Lakes Long Term Ecological Research Program. American Society of Testing and Materials, Special Technical testing Publication 894, 2233.Google Scholar
Kratz, T. K., Cook, R. B., Bowser, C. J. & Brezonik, P. L. 1987. Winter and spring pH depression in northern Wisconsin lakes caused by increases in pCO2. Canadian Journal of Fisheries and Aquatic Sciences 44, 1082–8.CrossRefGoogle Scholar
Levine, S. N. & Schindler, D. W. 1991. Modification of the N:P ratio in lakes through in-situ processes. Limnology and Oceanography (in review).Google Scholar
Mach, C. E. 1991. Chemistry of Al, Fe, Mn, Cd, Cu, Pb, and Zn in an experimentally acidified lake, Ph.D. thesis, Univ. of Minnesota, Minneapolis.Google Scholar
Malley, D. F. 1980. Decreased survival and calcium uptake by the crayfish Orconectes virilis in low pH. Canadian Journal of Fisheries and Aquatic Sciences 37, 364–72.CrossRefGoogle Scholar
Malley, D. F. & Chang, P. S. S. 1986. Increases in the abundance of Cladocera at pH 5.1 in experimentally-acidified Lake 223, Experimental Lakes Area, Ontario. Water, Air and Soil Pollution 30, 629–38.CrossRefGoogle Scholar
Malley, D. F., Findlay, D. L. & Chang, P. S. S. 1982. Ecological effects of acid precipitation on zooplankton. In Acid Precipitation: Effects on Ecological Systems, pp. 297327, ed., D'Itri, F. M. Ann Arbor, Michigan: Ann Arbor Science.Google Scholar
Matuszek, J. E., Goodier, J. & Wales, D. L. 1990. The occurrence of cyprinids and other small fish species in relation to pH in Ontario lakes. Transactions of the American Fisheries Society (in press).2.3.CO;2>CrossRefGoogle Scholar
Mills, K. H. & Schindler, D. W. 1986. Biological indicators of lake acidification. Water, Air and Soil Pollution 30, 779–89.CrossRefGoogle Scholar
Mills, K. H., Chalanchuk, S. M., Mohr, L. C. & Davies, I. J. 1987. Responses of fish populations to 8 years of experimental acidification. Canadian Journal of Fisheries and Aquatic Sciences 44 (Suppl. 1), 114–25.CrossRefGoogle Scholar
Mohr, L. C., Mills, K. H. & Klaverkamp, J. F. 1990. Survival and development of lake trout (Sahelinus namaycush) embryos in an acidified lake in northwestern Ontario. Canadian Journal of Fisheries and Aquatic Sciences 47, 236–43.CrossRefGoogle Scholar
Nero, R. W. & Schindler, D. W. 1983. Decline in Mysis relicta during acidification of Lake 223. Canadian Journal of Fisheries and Aquatic Sciences 40, 1905.CrossRefGoogle Scholar
Nicholls, K. H., Beaver, J. L. & Estabrook, R. H. 1982. Lakewide odours in Ontario and New Hampshire caused by Chrysochromulina breviturria. Nich. (Prymnesiophyceae). Hydrobiologia 96, 91–5.CrossRefGoogle Scholar
Norton, S., Mitchell, M., Kahl, J. & Brewer, G. 1988. In-lake alkalinity generation by sulfate reduction: A paleolimnological assessment. Water, Air and Soil Pollution 39, 3345.CrossRefGoogle Scholar
Okwueze, E. 1983. Geophysical investigations of the bedrock and groundwater-lake flow system in the Trout Lake region of Vilas county, northern Wisconsin. Ph.D. thesis, University of Wisconsin, Madison.Google Scholar
Raddum, G. & Fjellheim, A. 1984. Acidification and early warning organisms in freshwater of western Norway. Verhandlungen Internationale Vereinigung für Limnologie 22, 1973–80.Google Scholar
Rahel, F. J. & Magnuson, J. J. 1983. Low pH and the absence of fish species in naturally acidic Wisconsin lakes: inferences for cultural acidification. Canadian Journal of Fisheries and Aquatic Sciences 40, 39.CrossRefGoogle Scholar
RMCC (Federal-Provincial Research and Monitoring Coordinating Committee of Canada). 1990. The 1990 Canadian long-range transport of air pollutants and deposition assessment report. Part 4: aquatic effects.Google Scholar
Rudd, J. W. M., Kelly, C. A., St. Louis, V., Hesslein, R. H., Furutani, A. & Holoka, M. 1986. Microbial consumption of nitric and sulfuric acids in acidified north temperate lakes. Limnology and Oceanography 31, 1267–80.CrossRefGoogle Scholar
Rudd, J. W. M., Kelly, C. A., Schindler, D. W. & Turner, M. A. 1988. Disruption of the nitrogen cycle in acidified lakes. Science 240, 1515.CrossRefGoogle ScholarPubMed
Rudd, J. W. M., Kelly, C. A., Schindler, D. W. & Turner, M. A. 1990. A comparison of the acidification efficiencies of nitric and sulfuric acids by two whole-lake addition experiments. Limnology and Oceanography 35, 663–79.CrossRefGoogle Scholar
Schaffer, P. W., Hooger, R. P., Eschleman, K. N. & Church, M. R. 1988. Watershed vs. in-lake alkalinity generation: a comparison of rates using input-output studies. Water, Air and Soil Pollution 39, 263–73.CrossRefGoogle Scholar
Schiff, S. L. & Anderson, R. F. 1987. Limnocorral studies of chemical and biological acid neutralization in two freshwater lakes. Canadian Journal of Fisheries and Aquatic Sciences 44 (Suppl. 1), 173–87.CrossRefGoogle Scholar
Schindler, D. W. 1980. Experimental acidification of a whole lake: a test of the oligotrophication hypothesis. In Ecological Impact of Acid Precipitation, pp. 370–4, eds, Drablos, D. & Tollan, A. Oslo, Norway: SNSF Project.Google Scholar
Schindler, D. W. 1986. The significance of in-lake production of alkalinity. Water, Air and Soil Pollution 30, 931–44.CrossRefGoogle Scholar
Schindler, D. W. 1987. Recovery of Canadian lakes from acidification. In Reversibility of Acidification, pp. 213, ed., Barth, H. New York: Elsevier Applied Science.Google Scholar
Schindler, D. W. 1988. Experimental studies of chemical stressors on whole lake ecosystems. Verliandlungen Internationale Vereinigung für Limnologie 23, 1141.Google Scholar
Schindler, D. W. 1989. Different interpretations of the importance of internal alkalinity generation in the alkalinity budgets of lakes and watersheds: a response to Schaffer, P. W., Hooger, R. P., Eschelman, K. N. and Church, M. R. Water, Air and Soil Pollution 47, 175–7.CrossRefGoogle Scholar
Schindler, D. W. 1990. Experimental whole lake perturbations as tests of ecosystem theory. Oikos 57, 2541.CrossRefGoogle Scholar
Schindler, D. W. & Holmgren, S. K. 1971. Primary production and phytoplankton in the Experimental Lakes Area, northwestern Ontario, and other low-carbonate waters, and a liquid scintillation method for determining 14C activity in photosynthesis. Journal of the Fisheries Research Board of Canada 28, 189201.CrossRefGoogle Scholar
Schindler, D. W., Fee, E. J. & Ruszczynski, T. 1978. Phosphorus input and its consequences for standing crop and production in the Experimental Lakes Area and in similar lakes. Journal of the Fisheries Research Board of Canada 35, 190–6.CrossRefGoogle Scholar
Schindler, D. W., Ruszczynski, T. & Fee, E. J. 1980. Hypolimnion injection of nutrient effluents as a method for reducing eutrophication. Canadian Journal of Fisheries and Aquatic Sciences 37, 320–7.CrossRefGoogle Scholar
Schindler, D. W., Mills, K. H., Malley, D. F., Findlay, D. L., Shearer, J. A., Davies, I. J., Turner, M. A., Linsey, G. A. & Cruikshank, D. R. 1985a. Long term ecosystem stress: the effect of years of acidification on a small lake. Science 228, 13951401.CrossRefGoogle ScholarPubMed
Schindler, D. W., Turner, M. A. & Hesslein, R. H. 1985b. Acidification and alkalinization of lakes by experimental addition of nitrogen compounds. Biogeochemistry 1, 117–33.CrossRefGoogle Scholar
Schindler, D. W., Turner, M. A., Stainton, M. P. & Linsey, G. A. 1986. Natural sources of acid neutralizing capacity in low alkalinity lakes of the Precambrian Shield. Science 232, 844–7.CrossRefGoogle ScholarPubMed
Schindler, D. W., Beaty, K. G., Fee, E. J., Cruikshank, D. R., DeBruyn, E. R., Findlay, D. L., Linsey, G. A., Shearer, J. A., Stainton, M. P. & Turner, M. A. 1990. Effects of climatic warming on lakes of the central boreal forest. Science 250, 967–70.CrossRefGoogle Scholar
Schindler, D. W., Bayley, S. E., Curtis, P. J., Parker, B. R., Stainton, M. P. & Kelly, C. A. 1991. Synchronization of the carbon, nitrogen and phosphorus cycles in freshwater lakes. Hydrobiologia (in press).Google Scholar
Shearer, J. A. & De Bruyn, E. R. 1986. Phytoplankton productivity responses to direct addition of sulfuric and nitric acids to the waters of a double-basin lake. Water, Air and Soil Pollution 30, 695702.CrossRefGoogle Scholar
Shearer, J. A., Fee, E. J., DeBruyn, E. R. & DeClercq, D. R. 1987. Phytoplankton primary production and light attentuation responses to the acidification of a small Canadian Shield lake. Canadian Journal of Fisheries and Aquatic Sciences 44 (Suppl. 1), 8390.CrossRefGoogle Scholar
Siegfried, C. A., Bloomfield, J. A. & Sutherland, J. W. 1989. Planktonic rotifer community structure in Adirondack. New York, U.S.A., lakes in relation to acidity, trophic status and related water quality characteristics. Hydrobiologia 175, 3348.CrossRefGoogle Scholar
Sierszen, M. E. & Frost, T. M. 1990. Effects of lake acidification on zooplankton feeding rates and selectivity. Canadian Journal of Fisheries and Aquatic Sciences 47, 772–9.CrossRefGoogle Scholar
Siver, P. A. & Hamer, J. S. 1989. Multivariate statistical analysis of the factors controlling the distribution of scaled chrysophytes. Limnology and Oceanography 34, 368–81.CrossRefGoogle Scholar
Smol, J. P. & Dixit, S. S. 1990. Patterns of pH change inferred from chrysophyte microfossils in Adirondack and New England lakes. Journal of Paleolimnology 4, 3141.CrossRefGoogle Scholar
SPR Associates Inc. 1986. Estimation of the presence and impact of filamentous and odour-producing algae: a survey of cottagers on 214 Ontario recreational lakes. Ontario Ministry of Environment Report. 86 pp.Google Scholar
Stephenson, M. & Mackie, G. A. 1986. Lake acidification as a limiting factor in the distribution of the freshwater amphipod Hyalella azteca. Canadian Journal of Fisheries and Aquatic Sciences 43, 511–15.CrossRefGoogle Scholar
Stokes, P. M. 1981. Benthic algal communities in acidic lakes. In Effects of Acidification on Benthos, pp. 119–38, ed., Singer, R. New York: Canterbury Press.Google Scholar
Stokes, P. M. 1986. Ecological effects of acidification on primary producers in aquatic systems. Water, Air and Soil Pollution 30, 421–38.CrossRefGoogle Scholar
Stokes, P. M. & Yung, Y. K. 1986. Phytoplankton in selected LaCloche (Ontario) lakes, pH 4.2–7.0. with special reference to algae as indicators of chemical conditions. In Diatoms and Lake Acidity, pp. 5772. eds, Smol, J. P., Battarbee, R. W., Davis, R. B. & Merilainen, J. The Hague: W. Junk.CrossRefGoogle Scholar
Swenson, W. A., McCormick, J. H., Simonson, T. D., Jensen, K. M. & Eaton, J. G. 1989. Experimental acidification of Little Rock Lake (Wisconsin): Fish research approach and early responses. Archives of Environmental Contamination Toxicology 18, 167–74.CrossRefGoogle Scholar
Thompson, M. E. 1986. The cation denudation model: its continued validity. Water, Air and Soil Pollution 31, 1726.CrossRefGoogle Scholar
Turner, M. A., Jackson, M. B., Findlay, D. L., Graham, R. W., De Bruyn, E. R. & Vandermeer, E. M. 1987. Early responses of periphyton to experimental lake acidification. Canadian Journal of Fisheries and Aquatic Sciences 44 (Suppl. 1), 135–49.CrossRefGoogle Scholar
Turner, M. A., Howell, E. T., Summerby, M., Hesslein, R. H., Findlay, D. & Jackson, M. 1991. Changes in epilithic and epiphytic periphyton associated with lake acidification to pH 5. Limnology and Oceanography 36 (in press).CrossRefGoogle Scholar
Turner, M. A., Schindler, D. W., Jackson, M. B. & Findlay, D. F. Acidification-induced disruption of energetics in the littoral zone. In prep.Google Scholar
Watras, C. J. & Baker, A. L. 1988. The spectral distribution of downwelling light in northern Wisconsin lakes. Archiv für Hydrobiologie 112, 481–94.CrossRefGoogle Scholar
Watras, C. J. & Frost, T. M. 1989. Little Rock Lake (Wisconsin): Perspectives on an experimental ecosystem approach to seepage lake acidification. Archives of Environmental Contamination and Toxicology 18, 157–65.CrossRefGoogle Scholar
Webster, K. E., Frost, T. M., Watras, C. J., Swenson, W. A., Gonzalez, M. J. & Garrison, P. J. 1991. Complex biological responses to the experimental acidification of Little Rock Lake, Wisconsin (USA). Environmental Pollution (in press).CrossRefGoogle Scholar
Wehr, J. D., Brown, L. M. & O'Grady, K. A. 1987. Highly specialized nitrogen metabolism in a freshwater phytoplankter. Chrysochromulina brevituttita. Canadian Journal of Fisheries and Aquatic Sciences 44, 736–42.CrossRefGoogle Scholar
Wei, Y.-X., Yung, Y.-K., Jackson, M. B. & Sawa, T. 1989. Some Zygnematacea (Chlorophyta) of Ontario, Canada, including descriptions of two new species. Canadian Journal of Botany 67, 3233–47.CrossRefGoogle Scholar
Weir, E. P. 1989. Acid neutralization processes in Little Rock Lake, Wisconsin: laboratory and whole-lake observations. M.S. thesis, Univ. Minnesota, Minneapolis.Google Scholar
Wright, R. F., Lotse, E. & Semb, A. 1988. Reversiblity of acidification shown by whole-catchment experiments. Nature 334, 670–5.CrossRefGoogle Scholar
Yan, N. D., Keller, W., Pitblado, J. R. & Mackie, G. L. 1988. Daphnia-Holopedium relationships in Canadian Shield lakes ranging in acidity. Verhandlungen Internationale Vereinigung für Limnologie 23, 252–7.Google Scholar