, Volume 11, Issue 1, pp 67–86 | Cite as

Changes in community composition and biomass inJuncus roemerianus scheele andSpartina bakeri merr. marshes one year after a fire

  • Paul A. Schmalzer
  • C. Ross Hinkle
  • Joseph L. Mailander


Fires occur naturally in many wetlands and are widely used for marsh management. We examined the responses to fire ofJuncus roemerianus andSpartina bakeri marshes on Kennedy Space Center, Florida. In each marsh, we determined vegetation cover before burning on 5 permanent 15 m transects in the greater than 0.5 m and less than 0.5 m layers and sampled biomass on 25 plots (0.25 m2). One year after burning, we repeated the sampling. Species composition one year after burning was similar to that before the fire in bothJuncus andSpartina marshes. Minor species tended to increase, but this was significant only in the less than 0.5 m layer. In mixed stands, fire appeared to favorSpartina bakeri. Total cover (sum of the cover values for each species) in both marshes reestablished by one year after burning. Biomass did not recover as rapidly. In theJuncus marsh one year after burning, live biomass was 47.2%, standing dead 18.7%, and total biomass 29.3% of that before burning. In theSpartina marsh, biomass one year after burning was live 42.3%, standing dead 21.4%, and total 30.7% of that before burning. Fire increased the ratio of live to dead biomass from 0.82 before burning to 1.85 one year after the fire in theJuncus marsh. In theSpartina marsh, the ratio of live to dead biomass increased from 0.80 before burning to 1.59 one year after burning.

Key Words

biomass fire Juncus roemerianus marshes Spartina bakeri species diversity wetlands 


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Literature Cited

  1. Adrian, F. W., R. C. Lee, Jr., and J. E. Sasser. 1983. Upland management plan for Merritt Island National Wildlife Refuge. U. S. Fish and Wildlife Service, Merritt Island National Wildlife Refuge, Titusville, FL, USA.Google Scholar
  2. Chynoweth, L. A. 1975. Net primary production ofSpartina and species diversity of associated macroinvertebrates of a semi-impounded salt marsh. Technical Report No. 1, NASA, Kennedy Space Center, FL, USA.Google Scholar
  3. Clements, B. W. and A. J. Rogers. 1964. Studies of impounding for the control of saltmarsh mosquitoes in Florida, 1958–1963. Mosquito News 24: 265–276.Google Scholar
  4. Cohen, A. D. 1974. Evidence of fires in the ancient everglades and coastal swamps of southern Florida. p. 213–218.In P.J. Gleason (ed.) Environments of South Florida past and present. Miami Geological Society Memoir 2, Miami, FL, USA.Google Scholar
  5. Davison, K. L. 1986. Vegetation responses to fire on Cape Hatteras National Seashore, North Carolina. National Park Service Cooperative Park Studies Unit Technical Report 25. Institute of Ecology, University of Georgia, Athens, GA, USA.Google Scholar
  6. Davison, K. L. and S. P. Bratton. 1986. The vegetation history of Canaveral National Seashore Florida. National Park Service Cooperative Park Studies Unit Technical Report 22. Institute of Ecology, University of Georgia, Athens, GA, USA.Google Scholar
  7. Davison, K. L. and S. P. Bratton. 1988. Vegetation response and regrowth after fire on Cumberland Island National Seashore, Georgia. Castanea 53: 47–65.Google Scholar
  8. De la Cruz, A. A. 1974. Primary productivity of coastal marshes in Mississippi. Gulf Research Reports 4: 351–356.Google Scholar
  9. Duever, M. J., J. E. Carlson, J. F. Meeder, L. C. Duever, L. H. Gunderson, L. A. Riopelle, T. R. Alexander, R.L. Myers, and D. P. Spangler. 1986. The Big Cypress National Preserve. National Audubon Society Research Report No. 8, New York, NY, USA.Google Scholar
  10. Eleuterius, L. N. 1972. The marshes of Mississippi. Castanea 37: 153–168.Google Scholar
  11. Eleuterius, L. N. 1976. The distribution ofJuncus roemerianus in the salt marshes of North America. Chesapeake Science 17:289–292.CrossRefGoogle Scholar
  12. Eleuterius, L. N. 1984. Antecology of the black needlerush,Juncus roemerianus. Gulf Research Reports 7: 339–350.Google Scholar
  13. Eleuterius, L. N. and J. D. Caldwell. 1981. Growth kinetics and longevity of the salt marsh rushJuncus roemerianus. Gulf Research Reports 7: 27–34.Google Scholar
  14. Eleuterius, L. N. and F. C. Lanning. 1987. Silica in relation to leaf decomposition ofJuncus roemerianus. Journal of Coastal Research 3: 531–534.Google Scholar
  15. Faulkner, S. P. and A. A. de la Cruz. 1982. Nutrient mobilization following winter fires in an irregularly flooded marsh. Journal of Environmental Quality 11: 129–133.CrossRefGoogle Scholar
  16. Gallagher, J. L., R. J. Reimold, R. A. Linthurst and V. J. Pfeiffer. 1980. Aerial production, mortality, and mineral accumulation-export dynamics inSpartina alterniflora andJuncus roemerianus plant stands in a Georgia salt marsh. Ecology 61: 303–312.CrossRefGoogle Scholar
  17. Godfrey, R. K. and J. W. Wooten. 1979. Aquatic and Wetland Plants of Southeastern United States: Monocotyledons. The University of Georgia Press, Athens, GA, USA.Google Scholar
  18. Goodwin, T. M. 1979. Waterfowl management practices employed in Florida and their effectiveness on native and migratory waterfowl populations. Florida Scientist 42: 123–129.Google Scholar
  19. Green, R. H. 1979. Sampling Design and Statistical Methods for Environmental Biologists. John Wiley & Sons, New York, NY, USA.Google Scholar
  20. Hackney, C. T. and A. A. de la Cruz. 1981. Effects of fire on brackish marsh communities: management implications. Wetlands 1: 75–86.Google Scholar
  21. Hackney, C. T. and A. A. de la Cruz. 1983. Effects of winter fire on the productivity and species composition of two brackish marsh communities in Mississippi. International Journal of Ecology and Environmental Science 9: 185–208.Google Scholar
  22. Hopkinson, C. S., J. G. Gosselink, and R. T. Parrondo. 1978. Above ground production of seven marsh plant species in coastal Louisiana. Ecology 59: 760–769.CrossRefGoogle Scholar
  23. Izlar, R. L. 1984. Some comments on fire and climate in the Okefenokee swamp-marsh complex. p. 70–85.In A. D. Cohen, D. J. Casagrande, M. J. Andrejko, and G. R. Best (eds.) The Okefenokee Swamp: Its Natural History, Geology, and Geochemistry. Wetland Surveys, Los Alamos, NM, USA.Google Scholar
  24. Kirby, R. E., S. J. Lewis, and T. N. Sexson. 1988. Fire in North American wetland ecosystems: an annotated bibliography. U.S. Fish and Wildlife Service Biological Report 88(1), Washington, DC, USA.Google Scholar
  25. Kurz, H. and K. Wagner. 1957. Tidal marshes of the Gulf and Atlantic Coasts of northern Florida and Charleston, South Carolina. Florida State University Studies 24: 1–168.Google Scholar
  26. Kushlan, J. L. 1990. Freshwater marshes. p. 324–363.In R. L. Myers and J. J. Ewel (eds.) Ecosystems of Florida. University of Central Florida Press, Orlando, FL, USA.Google Scholar
  27. Lee, R.C., Jr. W.P. Leenhouts, and J.E. Sasser. 1981. Fire management plan Merritt Island National Wildlife Refuge. U. S. Fish and Wildlife Service, Merritt Island National Wildlife Refuge, Titusville, FL, USA.Google Scholar
  28. Leenhouts, W. P. and J. L. Baker. 1982. Vegetation dynamics in Dusky Seaside Sparrow habitat on Merritt Island National Wildlife Refuge. Wildlife Society Bulletin 10: 127–132.Google Scholar
  29. Loveless, C. M. 1959. A study of the vegetation in the Florida everglades. Ecology 40: 1–9.CrossRefGoogle Scholar
  30. Lynch, J.J. 1941. The place of burning in management of the Gulf Coast refuges. Journal of Wildlife Management 5: 454–458.CrossRefGoogle Scholar
  31. Mailander, J. L. 1990. Climate of the Kennedy Space Center and vicinity. NASA Technical Memorandum 103498. Kennedy Space Center, FL, USA.Google Scholar
  32. Mallik, A. U. and R. W. Wein. 1986. Response of aTypha marsh community to draining, flooding, and seasonal burning. Canadian Journal of Botany 64: 2136–2143.CrossRefGoogle Scholar
  33. McAtee, J. W., C. J. Scifres, and D. L. Drawe. 1979. Improvement of Gulf cordgrass range with burning or shredding. Journal of Range Management 32: 372–375.CrossRefGoogle Scholar
  34. Montague, C. L. and R. G. Wiegert. 1990. Salt marshes. p. 481–516.In R. L. Myers and J. J. Ewel (eds.) Ecosystems of Florida. University of Central Florida Press, Orlando, FL, USA.Google Scholar
  35. Montague, C. L., A. V. Zale, and H. F. Percival. 1987. Ecological effects of coastal marsh impoundments: a review. Environmental Management. 11: 743–756.CrossRefGoogle Scholar
  36. Mueller-Dombois, D. and H. Ellenberg. 1974. Aims and Methods of Vegetation Ecology. John Wiley & Sons, New York, NY, USA.Google Scholar
  37. Odum, E. P. and M. E. Fanning. 1973. Comparison of the productivity ofSpartina alterniflora andSpartina cynosuroides in Georgia coastal marshes. Bulletin of the Georgia Academy of Science 31: 1–12.Google Scholar
  38. Penfound, W. T. and G. S. Hathaway. 1938. Plant communities in the marshland of southeastern Louisiana. Ecological Monographs 8: 1–56.CrossRefGoogle Scholar
  39. Provancha, M. J., P. A. Schmalzer, and C. R. Hinkle. 1986. Vegetation types. John F. Kennedy Space Center, Biomedical Operations and Research Office (Maps in Master Planning format, 1∶9600 scale, digitization by ERDAS, Inc.). NASA, Kennedy Space Center, FL, USA.Google Scholar
  40. Provost, M. W. 1959. Impounding salt marshes for mosquito control and its effects on bird life. Florida Naturalist 32: 163–170.Google Scholar
  41. Provost, M. W. 1969 Ecological control of salt marsh mosquitos with side benefits to birds. p. 193–206.In Tall Timbers Conference on Ecological Animal Control by Habitat Management. Tallahassee, FL, USA.Google Scholar
  42. Provost, M. W. 1977. Source reduction in salt-marsh mosquito control: past and future. Mosquito News 37: 689–698.Google Scholar
  43. Schmalzer, P. A. and C. R. Hinkle. 1985. A brief overview of plant communities and the status of selected plant species at John F. Kennedy Space Center, Florida. Report submitted to Biomedical Office, NASA, Kennedy Space Center, FL, USA.Google Scholar
  44. Smith, L. M. and J. A. Kadlec. 1985. Fire and herbivory in a Great Salt Lake marsh. Ecology 66: 259–265.CrossRefGoogle Scholar
  45. Smith, L. M., J. A. Kadlec, and P. V. Fonnesbeck. 1984. Effects of prescribed burning on nutritive quality of marsh plants in Utah. Journal of Wildlife Management 48: 285–288.CrossRefGoogle Scholar
  46. Steward, K. K. and W. H. Omes. 1975. The autecology of sawgrass in the Florida Everglades. Ecology 56: 162–171.CrossRefGoogle Scholar
  47. Sweet, H. C. 1976. A study of a diverse coastal ecosystem of the Atlantic coast of Florida: Botanical studies on Merritt Island. Final Report. NASA, Kennedy Space Center, FL, USA.Google Scholar
  48. Sykes, P. W., Jr. 1980. Decline and disappearance of the Dusky Seaside Sparrow from Merriu Island, Florida. American Brids 34: 728–737.Google Scholar
  49. Thompson, D. J. and J. M. Shay. 1985. The effects of fire onPhragmites australis in the Delta Marsh, Manitoba. Canadian Journal of Botany 63: 1864–1869.Google Scholar
  50. Thompson, D. J. and J. M. Shay. 1989. First-year response of aPhragmites marsh community to seasonal burning. Canadian Journal of Botany 67: 1448–1455.CrossRefGoogle Scholar
  51. Trost, C. H. 1964. Study of wildlife usage of salt marsh on east coast of Florida before and after impoundment for mosquito and sandfly control. Final Report. Florida State Board of Health Entomological Research Center, Vero Beach, FL, USA.Google Scholar
  52. Trost, C. H. 1968. Dusky Seaside Sparrow. p. 849–859.In A. C. Bent and O. L. Austin, Jr. (eds.) Life histories of North American cardinals, grosbeaks, buntings, towhees, finches, sparrows, and allies. United States National Museum Bulletin 237, Washington, DC, USA.Google Scholar
  53. Turner, M. G. 1987. Effects of grazing by feral horses, clipping, trampling, and burning on a Georgia salt marsh. Estuaries 10: 54–60.CrossRefGoogle Scholar
  54. VanArman, J. and R. Goodrick. 1979. Effects of fire on a Kissimmee River marsh. Florida Scientist 42:183–195.Google Scholar
  55. Viosca, P., Jr. 1931. Spontaneous combustion in the marshes of southern Louisiana. Ecology 12:439–442.CrossRefGoogle Scholar
  56. Vogl, R. J. 1973. Effects of fire on the plants and animals of a Florida wetland. American Midland Naturalist 89:334–347.CrossRefGoogle Scholar
  57. Wade, D. D. 1989. A prescribed fire in a Florida cordgrass swale. Proceedings of the 17th Tall Timbers Fire Ecology Conference (in press). Tallahassee, FL, USA.Google Scholar
  58. Wade, D., J. Ewel, and R. Hofstetter. 1980. Fire in south Florida ecosystems. USDA Forest Service General Technical Report SE-17. Southeastern Forest Experiment Station, Asheville, NC, USA.Google Scholar
  59. White, D. A., T. E. Weiss, J. M. Tropani, and L. B. Thien. 1978. Productivity and decomposition of the dominant salt marsh plants in Louisiana. Ecology 59:751–759.CrossRefGoogle Scholar
  60. White, W. A. 1958. Some geomorphic features of central peninsular Florida. Geological Bulletin No. 41. Florida Geological Survey, Tallahassee, FL, USA.Google Scholar
  61. White, W. A. 1970. The geomorphology of the Florida peninsula. Geological Bulletin No. 51. Bureau of Geology, Florida Department of Natural Resources, Tallahassee, FL, USA.Google Scholar
  62. Wilbur, R. B. and N. L. Christensen. 1983. Effects of fire on nutrient availability in a North Carolina Coastal Plain pocosin. American Midland Naturalist 110:54–61.CrossRefGoogle Scholar
  63. Williams, R. B. and M. B. Murdoch. 1972. Compartmental analysis of the production ofJuncus roemerianus in a North Carolina salt marsh. Chesapeake Science 13:69–79.CrossRefGoogle Scholar
  64. Wright, H. A. and A. W. Bailey. 1982. Fire Ecology United States and Southern Canada. John Wiley & Sons, New York, NY, USA.Google Scholar
  65. Wunderlin, R. P. 1982. Guide to the Vascular Plants of Central Florida. University Presses of Florida, Gainesville, FL, USA.Google Scholar
  66. Zontek, F. 1966. Prescribed burning on the St. Marks National Wildlife Refuge. Proceedings Tall Timbers Fire Ecology Conference 5:195–210, Tallahassee, FL, USA.Google Scholar

Copyright information

© Society of Wetland Scientists 1991

Authors and Affiliations

  • Paul A. Schmalzer
    • 1
  • C. Ross Hinkle
    • 1
  • Joseph L. Mailander
    • 1
  1. 1.The Bionetics CorporationNASA Biomedical Operations and Research OfficeKennedy Space Center

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