Irregularly Flooded Salt Marshes of the Gulf and Atlantic Coasts of the United States

  • Judy P. Stout


Salt marshes may be characterized on the basis of the frequency of tidal inundation into (a) regularly flooded — flooded by most high tides and (b) irregularly flooded — flooded infrequently in a pattern not related entirely to the local tidal regime (Uhler and Hotchkiss, 1968). Regularly flooded marshes are typically dominated by Spartina alterniflora (saltmarsh cordgrass) and have been extensively studied along the US Atlantic coast and Gulf of Mexico (see summaries by Day, Smith, Wagner and Wilmer, 1973; Cooper, 1974; Pomeroy and Wiegert, 1981). The black needlerush (Juncus roemerianus) is the dominant marsh plant of irregularly flooded marshes. Though considerable information has been developed concerning the structure and function of Gulf coast irregularly flooded marshes (Stout, 1984), little work beyond vegetational descriptions and primary productivity studies has been provided for Atlantic Juncus marshes (Marshall, 1974). Basic features of the two marsh types have been compared by de la Cruz (1980).


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  1. Bishop, T.D. (1981) The seasonal abundance of the molluscan fauna of a Juncus romerianus and a Spartina cynosuroides brackish tidal marsh in Mississippi. MS Thesis. University of Southwestern Louisiana, Lafayette. 72 pp.Google Scholar
  2. Cooper, A.W. (1974) Salt marshes. In H.T. Odum, B.J. Copeland and E.A. McMahan (eds), Coastal ecological systems of the United States. Vol. II, Conserv. Fnd., Washington, DC pp. 55–98Google Scholar
  3. Cooper, A.W. and Waits, E.D. (1973) Vegetation types in an irregularly flooded salt marsh on the North Carolina Outer Banks. J. Elisha Mitchell Sci. Soc., 88, 78–91Google Scholar
  4. Coultas, C.L. (1969) Some saline marsh soils in north Florida: part I. Soil Crop Sci. Soc. Fla. Proc., 29, 111–23Google Scholar
  5. Day, J.W. Jr, Smith, W.G., Wagner, P.R. and Wilmer, C.S. (1973) Community structure and carbon budget of a salt marsh and shallow bay estuarine system in Louisiana. Center for Wetland Resources, Louisiana State University Baton Rouge. Publ. No. LSU-SG-72–04. 80 pp.Google Scholar
  6. de la Cruz, A.A. (1974) Primary productivity of coastal marshes in Mississippi. Gulf Res. Rep., 4 (3), 351–6Google Scholar
  7. de la Cruz, A.A. (1980) Differences between South Atlantic and Gulf Coast marshes. In P.S. Markovits (ed.), Proc. US Fish Wildl. Serv. Workshop on Coastal Ecosystems of the Southeastern US, FWS/OBSS-80/59, pp. 10–20Google Scholar
  8. de la Cruz, A.A. and Gabriel, B.C. (1974) Caloric, elemental and nutritive changes in decomposing Juncus roemerianus leaves. Ecology, 55, 882–6CrossRefGoogle Scholar
  9. de la Cruz, A.A. and Hackney, C.T. (1977) Energy value, elemental composition and productivity of below-ground biomass of a Juncus tidal marsh. Ecology, 58 (5), 1165–70CrossRefGoogle Scholar
  10. de la Cruz, A.A. and Poe, W.E. (1975) Amino acids in salt marsh detritus. Limnol. Oceanorg., 20 (1), 124–7CrossRefGoogle Scholar
  11. Eleuterius, L.N. (1976) The distribution of Juncus roemerianus in the salt marshes of North America. Chesapeake Sci., 17 (4), 289–92CrossRefGoogle Scholar
  12. Eleuterius, L.N. and Caldwell, J.D. (1981b) Colonizing patterns of tidal marsh plants and vegetational succession on dredge spoil in Mississippi. In R.H. Stovall (ed.), Proc. 8th Ann. Conf. Wetlands Restoration and Creation. Hillsborough Community College, Tampa, FL, pp. 74–86Google Scholar
  13. Eleuterius, L.N. and Eleuterius, C.K. (1979) Tide levels and salt marsh zonation. Bull. Mar. Sci., 29 (3), 394–400Google Scholar
  14. Foster, W.A. (1968) Studies on the distribution and growth of Juncus roemerianus in southeastern Brunswick Co. North Carolina. MS Thesis, North Carolina State University at Raleigh. 72 pp.Google Scholar
  15. Gabriel, B.C. and de la Cruz, A.A. (1974) Species composition, standing stock and net primary production of a salt marsh community in Mississippi. Chesapeake Sci., 15 (3), 72–7CrossRefGoogle Scholar
  16. Gallagher, J.L. (1974) Sampling macro-organic matter profiles in salt marsh plant root zones. Soil Sci. Soc. Am. Proc., 38 (1), 154–5CrossRefGoogle Scholar
  17. Gallagher, J.L., Reimold, R.J., Linthurst, R.A. and Pfeiffer, W.J. (1980) Aerial production, mortality and mineral accumulation-export dynamics in Spartina alterniflora and Juncus roemerianus plant stands in a Georgia salt marsh. Ecology, 61, 303–12CrossRefGoogle Scholar
  18. Giurgevich, J.R. and Dunn, E.L. (1978) Seasonal patterns of CO2 and water vapor exchange of Juncus roemerianus Scheele in a Georgia salt marsh. Am. J. Bot., 65 (5), 502–10CrossRefGoogle Scholar
  19. Gosselink, J.G., Hopkinson, C.S., Jr and Parrondo, R.T., (1977) Common marsh plant species of the Gulf Coast area. Vol. I, Productivity; Vol. II, Growth Dynamics. US Army COE, Dredged Material Research Program, Tech. Rept. D-7–44Google Scholar
  20. Hackney, C.T. (1977) Energy flux in a tidal creek draining an irregularly flooded Juncus marsh. PhD Dissertation. Mississippi State University, Mississippi State. 83 pp.Google Scholar
  21. Hackney, C.T. and Bishop, T.D. (1981) A note on relocation of marsh debris during a storm surge. Estuarine Coastal Mar. Sci., 12 (5), 621–4Google Scholar
  22. Hackney, C.T. and de la Cruz, A.A. (1978) Changes in interstitial water salinity of a Mississippi tidal marsh. Estuaries, 1 (3), 185–8CrossRefGoogle Scholar
  23. Hackney, C.T. and de la Cruz, A.A. (1979) Patterns of suspended particle transport in a Mississippi tidal marsh system. Gulf Res. Rep., 6 (3), 217–24Google Scholar
  24. Hackney, C.T. and de la Cruz, A.A. (1980) In situ decomposition of roots and rhizomes of two tidal marsh plants. Ecology, 61 (2), 226–31CrossRefGoogle Scholar
  25. Hackney, C.T. and de la Cruz, A.A. (1981a) Some notes on the macrofauna of an oligohaline tidal creek in Mississippi. Bull. Mar. Sci., 31 (3), 658–61Google Scholar
  26. Hackney, C.T. and de la Cruz, A.A. (1981b) Effects of fire on brackish marsh communities: management implications. Wetlands (J. Soc. Wetland Sci. ), 1, 75–86Google Scholar
  27. Hackney, C.T. and de la Cruz, A.A. (1982) The structure and function of brackish marshes in the north central Gulf of Mexico: a ten-year case study. In B. Gopal, R.E. Turner, R.G. Wetzel and D.F. Whigham (eds), Wetlands ecology and management. Natl. Inst. Ecol. Intl. Sci. Publ. Jaipur, India, pp. 89–107Google Scholar
  28. Hackney, C.T. and Haines, E.B. (1980) Stable carbon isotope composition of fauna and organic matter collected in a Mississippi estuary. Estuarine Coastal Mar. Sci., 10, 703–8Google Scholar
  29. Hackney, C.T., Stout, J.P. and de la Cruz, A.A. (1978) Standing crop and productivity of dominant marsh communities in the Alabama-Mississippi gulf coast. In Evaluation of the ecological role and techniques for the management of tidal marshes on the Mississippi and Alabama gulf coast. Miss.-Ala. Sea Grant Publ. No. MASGP-78–044, pp. I-1–29Google Scholar
  30. Harp, J.C. (1980) The meiofaunal communities associated with two salt marshes on Dauphin Island, Alabama, with emphasis on the benthic harpacticoid copepods. MS Thesis, University of South Alabama, Mobile. 82 pp.Google Scholar
  31. Heald, E.J. (1971) The production of organic detritus in a south Florida estuary. PhD Thesis, University of Miami, S.G. Tech. Bull. No. 6. Jan. 1971, 110 pp.Google Scholar
  32. Humphrey, W.D. (1979) Diversity, distribution and relative abundance of benthic fauna in a Mississippi tidal marsh. PhD Dissertation. Mississippi State University, Mississippi State, 93 pp.Google Scholar
  33. Ivester, M.S. (1978) Faunal dynamics. In L.R. Brown, de la Cruz, A.A., Ivester, M.S. and Stout, J.P. (eds), Evaluation of the ecological role and techniques for the management of tidal marshes on the Mississippi and Alabama Gulf Coast. Miss.-Ala. Sea Grant Publ. No. MASGP-78–044, pp. III-1–36Google Scholar
  34. Kilby, J.D. (1955) The fishes of two gulf coastal marsh areas of Florida. Tulane Stud. Zool., 2, 175–247Google Scholar
  35. Kraeuter, J.N. (1976) Biodeposition by salt marsh invertebrates. Mar. Biol., 35, 215–23Google Scholar
  36. Kruczynski, W.L., Subrahmanyam, C.B. and Drake, S.H. (1978a) Studies on the plant community of a North Florida salt marsh. Part I. Primary production. Bull. Mar. Sci., 28 (2), 316–34Google Scholar
  37. Kruczynski, W.L., Subrahmanyam, C.B. and Drake, S.H. (1978b) Studies on the plant community of a north Florida salt marsh. Part II. Nutritive value and decomposition. Bull. Mar. Sci., 28, 707–15Google Scholar
  38. Kurz, H. and Wagner, D. (1957) Tidal marshes of the gulf and atlantic coasts of north Florida and Charleston, South Carolina. Florida State University Stud., 24, 1–168Google Scholar
  39. Lindberg, S.E. and Harriss, R.C. (1973) Mechanisms controlling pore water salinities in a salt marsh. Limnol. Oceanogr., 18 (5), 788–91CrossRefGoogle Scholar
  40. Marshall, H.L. (1974) Irregularly flooded marsh. In H.T. Odum, B.J. Copeland and E.A. McMahan (eds), Coastal ecological systems of the United States, Vol. II, Censerv. Fnd., Washington, DC pp. 150–70Google Scholar
  41. Milner, C. and Hughes, R.E. (1968) Methods for the measurement of the primary production of grassland. International Biology Program Handbook. No. 6, Blackwell Scientific, Oxford, England, 70 pp.Google Scholar
  42. NOAA (1985) National estuarine inventory. Data atlas. Vol. I. Physical and hydrologic characteristics. US Dept. of Commerce, NOAA, National Ocean ServiceGoogle Scholar
  43. Parsons, K.A. (1978) Insect population diversity and the effects of grasshopper (Orthoptera: Tetigoniidae) grazing on the energy flow of a Mississippi Juncus roemerianus marsh. MS Thesis. Mississippi State University, Mississippi State, 37 pp.Google Scholar
  44. Parsons, K.A. and de la Cruz, A.A. (1980) Energy flow and grazing behavior of conocephaline grasshoppers in a Juncus roemerianus marsh. Ecology, 61 (5); 1045–50CrossRefGoogle Scholar
  45. Penfound, W.T. and Hathaway, E.S. (1983) Plant communities in the marshlands of southeast La. Ecol. Monogr., 8, 1–56Google Scholar
  46. Pomeroy, L.R. and Wiegert, R.G. (1981) The ecology of a salt marsh. Springer-Verlag, New York, 271 pp.CrossRefGoogle Scholar
  47. Sage, W.W. and Sullivan, M.J. (1978) Distribution of bluegreen algae in a Mississippi gulf coast salt marsh. J. Phycol., 14, 333–7CrossRefGoogle Scholar
  48. Smalley, R. (1959) The growth cycle of Spartina and its relation to the insect populations in the marsh. In Proc. Salt Marsh Conference, Sapelo Island, Georgia pp. 96–100Google Scholar
  49. Stalter, R. (1968) An ecological study of a South Carolina salt marsh. PhD Thesis, University of South Carolina, Charleston, SCGoogle Scholar
  50. Stout, J.P. (1978) An analysis of annual growth and productivity of Juncus roemerianus Scheele and Spartina alterniflora Loisel in coastal Alabama. PhD Thesis. University of Alabama, Tuscaloosa, 95 pp.Google Scholar
  51. Stout, J.P. (1984) The ecology of irregularly flooded salt marshes of the northeastern Gulf of Mexico: A community profile. US Fish Wildl. Serv. Biol. Rep., 85 (7.1), 98 pp.Google Scholar
  52. Stout, J.P. and de la Cruz, A.A. (1978) In situ decomposition of dead tissues of selected tidal marsh plants. In L.R. Brown, A.A. de la Cruz, M.S. Ivester and J.P. Stout (eds), Evaluation of the ecological role and techniques for the management of tidal marshes on the Mississippi and Alabama gulf coast. Miss.-Ala. Sea Grant Publ. MASGP-78–044, pp. I-50–9Google Scholar
  53. Subrahmanyam, C.B. and Coultas, C.L. (1980) Studies on the animal communities in two north Florida salt marshes. Part III. Seasonal fluctuations of fish and macroinvertebrates. Bull. Mar. Sci., 30 (4), 790–818Google Scholar
  54. Subrahmanyam, C.B. and Drake, S.H. (1975) Studies of the animal communities in two north Florida salt marshes. I. Fish communities. Bull. Mar. Sci., 25, 445–65Google Scholar
  55. Subrahmanyam, C.B., Kruczynski, W.L. and Drake, S.H. (1976) Studies on the animal communities in two north Florida salt marshes. Part II. Macroinvertebrate communities. Bull. Mar. Sci., 26 (2), 172–95Google Scholar
  56. Sullivan, M.J. (1975) Diatom communities from a Delaware salt marsh. J. Phycol., 11, 384–90Google Scholar
  57. Sullivan, M.J. (1977) Edaphic diatom communities associated with Spartina alterniflora and S. patens in New Jersey. Hydro-biologia, 52, 207–11CrossRefGoogle Scholar
  58. Sullivan, M.J. (1978) Diatom community structure: taxonomic and statistical analysis of a Mississippi salt marsh. J. Phycol., 14, 468–75CrossRefGoogle Scholar
  59. Sullivan, M.J. (1981) Effects of canopy removal and nitrogen enrichment on a Distichlis spicata–edaphic diatom complex. Estuarine Coastal Shelf Sci., 13, 119–29CrossRefGoogle Scholar
  60. Sullivan, M.J. (1982) Similarity of an ephiphytic and edaphic diatom community associated with Spartina alterniflora. Trans. Am. Microsc. Soc., 101 (1), 84–90CrossRefGoogle Scholar
  61. Uhler, F.M. and Hotchkiss, N. (1968) Vegetation and its succession in marshes and estuaries along the South Atlantic and gulf coasts. In Proc. Marsh Estuary Mgmt. Symp., Louisiana State University, Baton Rouge, pp. 26–32Google Scholar
  62. Waits, E.D. (1967) Net primary productivity of an irregularly flooded North Carolina salt marsh. PhD Dissertation. North Carolina State University, Raleigh, 113 pp.Google Scholar
  63. Wiegert, R.G. and Evans, F.C. (1964) Primary production and the disappearance of dead vegetation of an old field in southeastern Michigan. Ecology, 45, 49–62CrossRefGoogle Scholar
  64. Williams, R.B. and Murdoch, M.B. (1968) Compartmental analysis of production and decay of Juncus roemerianus. Abstract. ASB Bull., 15 (2), 59Google Scholar
  65. Williams, R.B. and Murdoch, M.B. (1972) Compartmental analysis of the production of Juncus roemerianus in a North Carolina salt marsh. Chesapeake Sci., 13, 69–79CrossRefGoogle Scholar
  66. Zilberberg, M.H. (1966) Seasonal occurrence of fishes in a coastal marsh of northwest Florida. Publ. Inst. Mar. Sic. Univ. Tex., 11, 126–34Google Scholar

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© Donal D. Hook 1988

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  • Judy P. Stout

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