Skip to main content
Log in

Zooplankton communities of restored depressional wetlands in wisconsin, USA

  • Published:
Wetlands Aims and scope Submit manuscript

Abstract

Wisconsin has lost approximately 2 million hectares of wetland since statehood (1848). Through the combined efforts of state and federal agencies and private groups focused primarily on wetland restoration for waterfowl habitat management or compensatory mitigation, a fairly substantial gain in wetland area has been achieved. Much of the wetland restoration effort in Wisconsin has occurred on formerly agricultural lands. However, due to the nature of the past disturbance and possible residual effects not corrected by simply returning surface waters to these lands, there is some question regarding the resultant wetland quality or biological integrity. In an effort aimed at developing tools to measure wetland gains in terms of quality or ecological integrity, the Wisconsin Department of Natural Resources (WDNR) initiated a study of biological communities on restored wetlands in Wisconsin. In this paper, we report on the community of microcrustaceans and arthropods that can be collected with a plankton net in open water in wetlands. We examined zooplankton community structure in restored wetlands in terms of richness, taxonomic representation, and Daphnia sexual reproduction and related these metrics to attributes on wetlands representing least-disturbed conditions and agriculturally impacted wetlands. We sampled 56 palustrine wetlands distributed across Wisconsin. These wetland sites were categorized as agricultural, least-impacted, and restored (recently withdrawn from agricultural usage). The wetlands were reasonably homogeneous in many ways, so that taxon richness was not correlated with basin origin, presence of adjacent roads, presence or absence of fish, water chemistry, or the size of the open water. We identified a total of 40 taxa. Taxon richness was significantly lower in agricultural sites (average of 3.88 taxa per site) compared to that of least-impacted sites (7.29 taxa) and restored sites (7.21 taxa). Taxon richness of restored sites was significantly correlated with time since restoration. The data indicate that taxon richness changes from a value typical of agricultural sites to the average richness of least-impacted sites in about 6.4 years. The total taxon list for 8 agricultural sites (14 taxa) was significantly smaller than the average value for randomly chosen sets of 8 least-impacted sites (20.4 taxa). Agricultural and least-impacted sites tended to have the same common taxa. Many taxa of chydorid cladocerans and cyclopoid copepods that were rare in least-impacted sites did not occur in the agricultural sites, nor did fairy shrimp occur in agricultural sites. Daphnia populations only produced males in least-impacted and restored sites. Further research is needed to identify the mechanism(s) responsible for the reduced species richness and lack of sexual reproduction in agricultural wetland sites. Likely factors include eutrophication, turbidity, or chemical contamination. We conclude that restoration of wetland watersheds works. Withdrawal of the watershed from agricultural usage is followed by an increase in taxon richness, and the sites resembled least-impacted sites in about 6–7 years.

This is a preview of subscription content, log in via an institution to check access.

Access this article

Price excludes VAT (USA)
Tax calculation will be finalised during checkout.

Instant access to the full article PDF.

Similar content being viewed by others

Literature Cited

  • APHA. 1989. Standard Methods for the Examination of Water and Wastewater. 17th edition. American Public Health Association. Washington, DC, USA.

    Google Scholar 

  • Beaver, J. R., A. M. Miller-Lemke, and J. K. Acton, 1999. Midsummer zooplankton assemblages in four types of wetlands in the Upper Midwest, USA. Hydrobiologia 380:209–220.

    Article  Google Scholar 

  • Brock, T. C. M., J. J. R. M. Vet, M. J. J. Kerkhofs, J. Lijzen, W. J. van Zuilekom, and R. Gijlstra. 1993. Archives of Environmental Contamination and Toxicology 25:160–169.

    Article  CAS  Google Scholar 

  • Danielson, T. J. 1998. Wetland bioassessment fact sheets. U.S. Environmental Protection Agency, Office of Wetlands, Oceans, and Watersheds, Wetlands Division, Washington, DC, USA. EPA843-F-98-001.

    Google Scholar 

  • Dodson, S. 1992. Predicting crustacean zooplankton species richness. Limnology and Oceanography 37:848–856.

    Google Scholar 

  • Dodson, S. I. and T. Hanazato. 1995. Comments on effects of anthropogenic and natural organic chemicals on the development of Daphnia, a key member of aquatic ecosystems. Environmental Health Perspectives 103 (Special Supplement No. 4): 7–11.

    Article  CAS  PubMed  Google Scholar 

  • Dodson, S. I., C. M. Merritt, L. Torrentera, K. M. Winter, C. K. Tornehl, and K. Girvin. 1999. Dieldrin reduces male production and sex ratio in Daphnia galeata mendotae. Toxicology and Industrial Health 15:192–199.

    Article  CAS  PubMed  Google Scholar 

  • Dodson, S. I., S. E. Arnott, and C. L. Cottingham. 2001. The Relationship in Lake Communities between Primary Productivity and Species Richness. Ecology 81:2662–2679.

    Google Scholar 

  • Fairchild, G. W., A. M. Faulds, and L. L. Saunders. 1999. Constructed marshes in southeast Pennsylvania—Invertebrate foodweb structure. p. 423–446. In D. P. Batzer, R. B. Rader, and S. A. Wissinger (eds.) Invertebrates in Freshwater Wetlands of North America: Ecology and Management. John Wiley & Sons, Inc. New York, NY, USA.

    Google Scholar 

  • Hessen, D. O., T. Källqvist, M. I. Abdel-Hamid, and D. Berge. 1994. Norwegian Journal of Agricultural Sciences Supplement No. 13: 153–161.

    Google Scholar 

  • Jak, R. G., J. L. Maas, and M. C. T. Scholten. 1998. Ecotoxicity of 3,4-dichloroaniline in enclosed freshwater plankton communities at different nutrient levels. Ecotoxicology 7:49–60.

    Article  CAS  Google Scholar 

  • Schell, J., C. J. Santos Flores, B. M. Hunker, S. Kloehn, A. Michelson, R. A. Lillie, and S. I. Dodson. 2001. Zooplankton of small lakes and wetland ponds in Wisconsin, USA. Hydrobiologia. In press.

  • Strauss, E. A., W. K. Dodds, and C. C. Edler. 1994. The impact of nutrient pulses on trophic interactions in a farm pond. Journal of Freshwater Ecology 9:217–228.

    CAS  Google Scholar 

  • Threlkeld, S. T. and D. M. Soballe. 1988. Effects of mineral turbidity on fresh-water plankton communities: 3 exploratory tank experiments of factorial design. Hydrobiologia 159:223–236.

    Article  CAS  Google Scholar 

  • Trochell, P., and T. Bernthal. 1998. Small wetlands and the cumulative impacts of small wetlands losses: a synopsis of the literature. Wisconsin Department of Natural Resources, Madison, WI, USA. Publ-FH226-98.

    Google Scholar 

  • VanRees-Siewert, K. L. and J. J. Dinsmore. 1996. Influence of wetland age on bird use of restored wetlands in Iowa. Wetlands 16: 577–582.

    Article  Google Scholar 

  • Williams, D. D. 1987. The Ecology of Temporary Waters. Timber Press, Portland, OR, USA.

    Google Scholar 

  • WDNR. 2000. Wisconsin water quality assessment report to Congress. Wisconsin Department of Natural Resources. Madison, WI, USA. Report 305(b).

    Google Scholar 

  • WSLH. 1997. Manual of Standard Operating Procedures—Inorganic Chemistry Unit. Wisconsin State Laboratory of Hygiene, University of Wisconsin, Madison, WI, USA. 53707-7996. Revised March 1997. Method 115. 1:1–4.

    Google Scholar 

Download references

Author information

Authors and Affiliations

Authors

Rights and permissions

Reprints and permissions

About this article

Cite this article

Dodson, S.I., Lillie, R.A. Zooplankton communities of restored depressional wetlands in wisconsin, USA. Wetlands 21, 292–300 (2001). https://doi.org/10.1672/0277-5212(2001)021[0292:ZCORDW]2.0.CO;2

Download citation

  • Received:

  • Revised:

  • Accepted:

  • Issue Date:

  • DOI: https://doi.org/10.1672/0277-5212(2001)021[0292:ZCORDW]2.0.CO;2

Key Words

Navigation