Skip to main content
Log in

Spatial and Temporal Hypoxia Dynamics in Dense Emergent Macrophytes in a Florida Lake

  • Original Paper
  • Published:
Wetlands Aims and scope Submit manuscript

Abstract

Many aquatic systems worldwide have experienced significant changes in littoral macrophyte communities from altered hydrology in the form of water controls structures (e.g., dams). Water level stabilization for flood control can cause persistent occurrence of dense stands of emergent macrophytes, which can affect the physicochemical environment for fishes. We evaluated dissolved oxygen (DO) concentrations in five emergent macrophyte species (cattail Typha spp., pickerelweed Pontedaria cordata, smartweed Polygonum spp., torpedograss Panicum repens, and water primrose Ludwigia spp.) at three levels of macrophyte coverage (i.e., 50–64, 65–79, and 80–95%) at Lake Istokpoga, Florida during July–August (summer) and October–November (fall) 2007. Dissolved oxygen exhibited substantial spatial and temporal variability at small scales (i.e., meters and hours), with the lowest DO and highest probability of hypoxia occurring in smartweed and water primrose habitats relative to other macrophyte types. The probability of hypoxia increased with macrophyte coverage for all macrophyte species tested. Dissolved oxygen was influenced by the structural differences (e.g., stem density and size) and spatial orientation (e.g., proximity to open water) associated with the individual macrophyte habitats. Restoration efforts that create open water pathways and maximize edge areas might improve DO concentrations and habitat quality and quantity for freshwater fishes.

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.

Fig. 1
Fig. 2
Fig. 3
Fig. 4
Fig. 5

Similar content being viewed by others

References

  • Akaike H (1974) A new look at the statistical model identification. IEEE Transactions on Automatic Control 19:716–723

    Article  Google Scholar 

  • Allen MS, Tugend K (2002) Effects of a large-scale habitat enhancement project on habitat quality for age-0 largemouth bass at Lake Kissimmee, Florida. In: Phillip DP, Ridgeway MS (eds) Black Bass: ecology, conservation, and management. American Fisheries Society, Maryland, pp 265–276

    Google Scholar 

  • Azza N, Denny P, Van De Koppel J, Kansiime F (2006) Floating mats: their occurrence and influence on shoreline distribution of emergent vegetation. Freshwater Biology 51:1286–1297

    Article  Google Scholar 

  • Boettcher EJ, Fineberg J, Lathrop D (2000) Turbulence and wave breaking effects on air-water gas exchange. Physical Review Letters 85:2030–2033

    Article  CAS  PubMed  Google Scholar 

  • Breitberg DL, Loher T, Pacey CA, Gernstein A (1997) Varying effects of low dissolved oxygen on trophic interactions in an estuarine food web. Ecological Monographs 67:489–507

    Article  Google Scholar 

  • Brenner M, Binford M, Deevey E (1990) Lakes. In: Myers RL, Ewel JJ (eds) Ecosystems of Florida. University of Central Florida Press, Florida, pp 364–390

    Google Scholar 

  • Bunch AJ (2008) Fish community composition and dissolved oxygen dynamics in dense emergent macrophyte stands at Lakes Istokpoga and Kissimmee, Florida. Thesis. University of Florida

  • Burleson ML, Wilheim D, Smatresk N (2001) The influence of fish size on the avoidance of hypoxia and oxygen selection by largemouth bass. Journal of Fish Biology 59:1336–1349

    Google Scholar 

  • Caraco N, Cole J, Findlay S, Wigand C (2006) Vascular plants as engineers of oxygen in aquatic systems. BioScience 56:219–225

    Article  Google Scholar 

  • Diaz RJ (2001) Overview of hypoxia around the world. Journal of Environmental Quality 30:275–281

    Article  CAS  PubMed  Google Scholar 

  • Eby LA, Crowder L, McClellan C, Peterson C, Powers J (2005) Habitat degradation of intermittent hypoxia: impacts on demersal fishes. Marine Ecological Progress Series 291:249–261

    Article  Google Scholar 

  • Fernandez C, Fernandez M, Becares E (1999) Influence of water-level fluctuation on the structure and composition of the macrophyte vegetation in two small temperate lakes in Northwest Spain. Hydrobiologia 415:155–162

    Article  Google Scholar 

  • Ferreira LV, Stohlgren TJ (1999) Effects of river level fluctuation on plant species richness, diversity, and distribution in a floodplain forest in Central Amazonia. Oecologia 120:582–587

    Article  Google Scholar 

  • Florida LAKEWATCH (2005) Data report. School of Forest Resources and Conservation, University of Florida. Available via http://lakewatch.ifas.ufl.edu/data2005.htm. Accessed 5 May 2008

  • Goodrick RL, Milleson J (1974) Studies of floodplain vegetation and water-level fluctuation in the Kissimmee River Valley. Technical Report 74-2. South Florida Water Management District, Central and Southern Florida Flood Control District, West Palm Beach, Florida

  • Graham JB (1997) Air-breathing fishes: evolution, diversity, and adaptation. Academic, San Diego

    Google Scholar 

  • Hamilton SK, Sippel S, Melack J (1995) Oxygen depletion and carbon dioxide and methane production in waters of the Pantanal wetland of Brazil. Biogeochemistry 30:115–141

    Article  CAS  Google Scholar 

  • Hudon C (1997) Impact of water-level fluctuation on St. Lawrence River aquatic vegetation. Canadian Journal of Fisheries and Aquatic Sciences 54:2853–2865

    Article  Google Scholar 

  • Keddy PA, Fraser L (2000) Four general principles for the management and conservation of wetlands in large lakes: the role of water levels, nutrients, competitive hierarchies and centrifugal organization. Lakes and Reservoirs: Research and Management 5:177–185

    Article  Google Scholar 

  • Keddy PA, Reznicek A (1986) Great Lakes vegetation dynamics: the role of fluctuating water levels and buried seeds. Journal of Great Lakes Research 12:25–36

    Article  Google Scholar 

  • Killgore KJ, Hoover J (2001) Effects of hypoxia on fish assemblages in a vegetated waterbody. Journal of Aquatic Plant Management 39:40–44

    Google Scholar 

  • Kramer DL (1987) Dissolved oxygen and fish behavior. Environmental Biology of Fishes 18:81–92

    Article  Google Scholar 

  • Lassen C, Revsbech N, Pedersen O (1997) Macrophyte development resuspension regulate the photosynthesis and production of benthic microalgae. Hydrobiologia 350:1–11

    Article  CAS  Google Scholar 

  • Lewis WM Jr (1970) Morphological adaptations of cyprinodontoids for inhabiting oxygen deficient waters. Copeia 1970:319–326

    Article  Google Scholar 

  • Leyer I (2005) Predicting plant species’ responses to river regulation: the role of water level fluctuations. Journal of Applied Ecology 42:239–250

    Article  Google Scholar 

  • Lightbody AF, Nepf H (2006) Prediction of near-field shear dispersion in an emergent canopy with heterogeneous morphology. Environmental Fluid Mechanics 6:477–488

    Article  Google Scholar 

  • Miranda LE, Driscoll M, Allen M (2000) Transient physiochemical microhabitats facilitate fish survival in inhospitable aquatic plant stands. Freshwater Biology 44:617–628

    Article  Google Scholar 

  • Moss DD, Scott D (1961) Dissolved-oxygen requirements of three species of fish. Transactions of the American Fisheries Society 90:377–393

    Article  CAS  Google Scholar 

  • Nepf HM (1999) Drag, turbulence, and diffusion in flow through emergent vegetation. Water Resources Research 35:479–489

    Article  Google Scholar 

  • Riis T, Hawes I (2002) Relationships between water-level fluctuation and vegetation diversity in shallow water of New Zealand lakes. Aquatic Botany 74:133–148

    Article  Google Scholar 

  • Rose C, Crumpton W (2006) Spatial patterns in dissolved oxygen and methane concentrations in prairie pothole wetlands in Iowa, USA. Wetlands 26:1020–1025

    Article  Google Scholar 

  • Smale MA, Rathbuni C (1995) Hypoxia and hyperthermia of headwater stream fishes. Transactions of the American Fisheries Society 124:698–710

    Article  Google Scholar 

  • Smith DH, Smart R, Hanlon C (2004) Influence of water level on torpedograss establishment in Lake Okeechobee, Florida. Lake and Reservoir Management 20:1–13

    Article  Google Scholar 

  • Steinman AD, Rosen B (2000) Lotic-lentic linkages associated with Lake Okeechobee, Florida. Journal of the North American Benthological Society 19:733–741

    Article  Google Scholar 

  • Toth LA, Melvin S, Arrington D (1998) Hydrologic manipulations of the channalized Kissimmee River. BioScience 48:757–764

    Article  Google Scholar 

  • Toth LA, Koebel J Jr, Warne A, Chamberlain J (2002) Implications of reestablishing prolonged flood pulse characteristics of the Kissimmee River and floodplain ecosystem. In: Middleton BA (ed) Flood pulsing in wetlands: restoring the natural hydrological balance. Wiley, New York, pp 191–221

    Google Scholar 

  • Webster JR, Benfield E (1986) Vascular plant breakdown in freshwater ecosystems. Annual Review of Ecology and Systematics 17:567–594

    Article  Google Scholar 

  • Wu RS (2002) Hypoxia: from molecular responses to ecosystem responses. Marine Pollution Bulletin 45:35–45

    Article  CAS  PubMed  Google Scholar 

Download references

Acknowledgments

The Florida Fish and Wildlife Conservation Commission provided funding for this research. Tim Bonvechio, Tim Coughlin, Larry Davis, Beacham Furse, Steve Gornak, and Craig Mallison provided critical insight on fish and macrophyte communities. Special thanks to Drew Dutterer, Patrick O’Rouke, Erika Thompson, and Allison Watts for help in the field. Matt Catalano and Mark Rogers provided help with analyses. Mike Netherland, Karl Havens, and anonymous reviewers provided useful editorial comments.

Author information

Authors and Affiliations

Authors

Corresponding author

Correspondence to Aaron J. Bunch.

Rights and permissions

Reprints and permissions

About this article

Cite this article

Bunch, A.J., Allen, M.S. & Gwinn, D.C. Spatial and Temporal Hypoxia Dynamics in Dense Emergent Macrophytes in a Florida Lake. Wetlands 30, 429–435 (2010). https://doi.org/10.1007/s13157-010-0051-9

Download citation

  • Received:

  • Accepted:

  • Published:

  • Issue Date:

  • DOI: https://doi.org/10.1007/s13157-010-0051-9

Keywords

Navigation