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Effects of tidally mediated litter moisture content on decomposition of Spartina alterniflora and S. patens

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Abstract

Relationships between flooding frequency, flooding duration, litter moisture levels, and litter decay rates were investigated across the natural hydrologic gradient common to intertidal salt marshes. The effects on litter decay of natural and experimental alterations of litter moisture content were assessed in both field litterbag experiments (conducted in a southern New Jersey salt marsh from 1989 to 1990) and laboratory incubations (1990). Overall, tidally mediated litter moisture content was the dominant factor controlling litter decay throughout the vegetated marsh. Rates of carbon loss were most closely related to litter moisture levels (r=0.84), which were directly related to flooding frequency (r=0.66) and duration (r=0.63). Litter moisture levels were related to elevation within the tidal range due to increasing surface levation from creekbank to high marsh (ca. 54 cm) and height of litter above the sediment surface. Carbon losses from litter of short and tall form Spartina alterniflora Loisel. and S. patens (Aiton) Muhl. along the marsh elevation gradient indicate that while some of the variations in decay rates may be due to litter type, litter moisture accounted for most of the observed variation between marsh zones and within each litter type. Mousture levels are also affected by the water retention capacity of each litter type, which may also secondarily influence decay rates. Short-term incubations of litter indicated that CO2 evolution was positively related to moisture content with negligible respiration at moisture levels below 15% (fresh mass), increasing to a maximum between 65 and 75% depending upon litter type. Since most Spartina spp. litter remains above the marsh surface where it maintains a lower moisture content than surface litter, the use of surface litterbags may overestimate rates of carbon loss in some systems. In addition, since changes in elevation of only a few centimeters had significant effects on both litter moisture levels and decay rates, slight changes in tidal regime may have important consequences for organic matter cycling in salt marshes by affecting litter decomposition processes.

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References

  • Burkholder PR, Bornside LM (1957) Decomposition of marsh grass by aerobic marine bacteria. Bull Torrey bot Club 84:366–383

    Google Scholar 

  • Christian RR (1984) A life-table approach to decomposition studies. Ecology 65(5):1693–1697

    Google Scholar 

  • de la Cruz AA (1973) The role of tidal marshes in the productivity of coastal waters. Bull Ass SEast Biologists 20(4):147–156

    Google Scholar 

  • Dame RF (1989) The importance of Spartina alterniflora to Atlantic Coast estuaries. Rev aquat Biol 1(4):639–660

    Google Scholar 

  • Day RW, Quinn GP (1989) Comparisons of treatment after an analysis of variance in ecology. Ecol Monogr 59(4):433–463

    Google Scholar 

  • Frasco BA, Good RE (1982) Decomposition dynamics of Spartina alterniflora and Spartina patens in a New Jersey salt marsh. Am J Bot 69(3):402–406

    Google Scholar 

  • Gallagher JL, Kibby HV, Skirvin KW (1984) Community respiration of decomposing plants in Oregon estuarine marshes. Estuar cstl Shelf Sci 18:421–431

    Google Scholar 

  • Gallagher JL, Pfeiffer WJ (1977) Aquatic metabolism of the communities associated with attached dead shoots of salt marsh plants. Limnol Oceanogr 22:562–565

    Google Scholar 

  • Good RE, Frasco BR (1979) Estuarine evaluation study: a four-year report of production and decomposition dynamics of salt marsh communities of the Manahawkin marshes, Ocean County, New Jersey Report to New Jersey Department of Environmental Protection Division of Fish, Game and Shellfisheries, Trenton, NJ. Rutgers University Center for Coastal and Environmental Studies CCES Publ. No. NJ/RU-DEP-11-9-79

  • Gosselink JG, Kirby CJ (1974) Decomposition of salt marsh grass, Spartina alterniflora Loisel. Limnol Oceanogr 19(3):825–832

    Google Scholar 

  • Haines EB, Hanson RB (1979) Experimental degradation of detritus made from the salt marsh plants Spartina alterniflora Loisel., Salicornia virginica L., and Juncus roemerianus Scheele. J exp mar Biol Ecol 40:27–40

    Google Scholar 

  • Hopkinson CS, Schubauer JP (1984) Static and dynamic aspects of nitrogen cycling in the salt marsh graminoid Spartina alterniflora. Ecology 65(3):961–969

    Google Scholar 

  • Howes BL, Dacey JWH, Teal JM (1985) Annual carbon mineralization and belowground production of Spartina alterniflora in a New England salt marsh. Ecology 66(2):595–605

    Google Scholar 

  • Kruczynski WL, Subrahmanyam CB, Drake SH (1978) Studies on the plant community of a north Florida salt marsh. Part II. Nutritive value and decomposition. Bull mar Sci 28(4):707–715

    Google Scholar 

  • Lee C, Howarth RW, Howes BL (1980) Sterols in decomposing Spartina alterniflora and the use of ergosterol in estimating the contribution of fungi to detrital nitrogen. Limnol Oceanogr 25(2):290–303

    Google Scholar 

  • Linthurst RA, Reimold RJ (1978) Estimated net aerial primary productivity for selected estuarine angiosperms in Maine, Delaware, and Georgia. Ecology 59(5):945–955

    Google Scholar 

  • Mann KH (1972) Macrophyte production and detritus food chains in coastal waters. Mem Ist Ital Idrobiol 29 (Suppl): 353–383

    Google Scholar 

  • Marinucci AC (1982) Trophic importance of Spartina alterniflora production and decomposition to the marsh-estuarine ecosystem. Biol Conserv 22:35–58

    Google Scholar 

  • Marinucci AC, Bartha R (1982) A component model of decomposition of Spartina alterniflora in a New Jersey salt marsh. Can J Bot 60:1618–1624

    Google Scholar 

  • Marinucci AC, Hobbie JE, Helfrich JVK (1983) Effect of litter nitrogen on decomposition and microbial biomass in Spartina alterniflord. Microb Ecol 9:27–40

    Google Scholar 

  • McKee KL, Seneca ED (1982) The influence of morphology in determining the decomposition of two salt marsh macrophytes. Estuaries 5(4):302–309

    Google Scholar 

  • Montagna PA, Ruber E (1980) Decomposition of Spartina alterniflora in different seasons and habitats of a northern Massachusetts salt marsh, and a comparison with other Atlantic regions. Estuaries 3(1):61–64

    Google Scholar 

  • Moran MA, Benner R, Hodson RE (1989) Kinetics of microbial degradation of vascular plant material in two wetland ecosystems. Oecologia 79:158–167

    Google Scholar 

  • Newell SY (1993) Decomposition of shoots of a salt-marsh grass. In: Jones JG (ed) Advances in microbial ecology. 13. University of Georgia, Sapelo Island, Georgia

    Google Scholar 

  • Newell SY, Arsuffi TL, Kemp PF, Scott LA (1991) Water potential of standing-dead shoots of an intertidal grass. Oecologia 85:321–326

    Google Scholar 

  • Newell SY, Fallon RD (1989) Litterbags, leaf tags, and decay of non-abscised intertidal leaves. Can J Bot 67:2324–2327

    Google Scholar 

  • Newell SY, Fallon RD, Miller JD (1989) Decomposition and microbial dynamics for standing, naturally positioned leaves of the salt-marsh grass Spartina alterniflora. Mar Biol 101:471–481

    Google Scholar 

  • Newell SY, Fallon RD, Rodriguez RMC, Groene LC (1985) Influence of rain, tidal wetting and relative humidity on release of carbon dioxide by standing-dead salt-marsh plants. Oecologia 68:73–79

    Google Scholar 

  • Nixon SW, Oviatt CA (1973) Ecology of a New England salt marsh. Ecol Monogr 43:463–498

    Google Scholar 

  • Odum EP, de la Cruz AA (1967) Particulate organic detritus in a Georgia salt marsh-estuarine ecosystem. In: Lauff GH (ed) Estuaries. American Association for the Advancement of Science Publ. 83., Washington, D.C.

  • Odum WE, Zieman JC, Heald EJ (1972) The importance of vascular plant detritus to estuaries. Proceedings of the coastal marsh and estuary management symposium. Louisiana State University, Baton Rouge, Louisiana

    Google Scholar 

  • Redfield AC (1972) Development of a New England salt marsh. Ecol Monogr 42:201–237

    Google Scholar 

  • Reice SR, Stiven AE (1983) Environmental patchiness, litter decomposition and associated faunal patterns in a Spartina alterniflora marsh. Estuar cstl Shelf Sci 16:559–571

    Google Scholar 

  • SAS Institute Inc. (1988) SAS/STATTM User's Guide, Release 6.03. SAS Institute, Cary, North Carolina

    Google Scholar 

  • Sokal RR, Rohlf FJ (1981) Biometry. WH Freeman and Company, New York, New York

    Google Scholar 

  • Stumm W, Morgan JJ (1970) Aquatic chemistry. Wiley-Interscience, New York, New York

    Google Scholar 

  • Swift MJ, Heal OW, Anderson JM (1979) Studies in ecology, Vol 5. Decomposition in terrestrial ecosystems. University of California Press, Berkeley, California

    Google Scholar 

  • Teal JM (1962) Energy flow in the salt marsh ecosystem of Georgia. Ecology 43(4):614–624

    Google Scholar 

  • Turner RE (1976) Geographic variations in salt marsh macrophyte production: a review. Contr mar Sci Univ Tex 20:47–68

    Google Scholar 

  • Valiela I, Howes B, Howarth R, Giblin A, Foreman K, Teal JM, Hobbie JE (1982) Regulation of primary production and decomposition in a salt marsh ecosystem. In: Gopal GP, Turner R, Wetzel R, Whigham D (eds) Wetlands: ecology and management. National Institute of Ecology. Jaipur, India

    Google Scholar 

  • Valiela I, Wilson J, Buchsbaum R, Rietsma C, Bryant D, Foreman K, Teal J (1984) Importance of chemical compotition of salt marsh litter on decay rates and feeding by detritivores. Bull mar Sci 35(3):261–269

    Google Scholar 

  • Valiela I, Teal JM, Allen SD, Van Etten R, Goehringer D, Volkmann S (1985) Decomposition in salt marsh ecosystems: the phases and major factors affecting disappearance of above-ground organic matter. J exp mar Biol Ecol 89:29–54

    Google Scholar 

  • Vince SW, Valiela I, Teal J (1981) An experimental study of the structure of herbivorous insect communities in a salt marsh. Ecology 62(6):1662–1678

    Google Scholar 

  • White DA, Trapani JM (1982) Factors influencing disappearance of Spartina alterniflora from litterbags. Ecology 63(1):242–245

    Google Scholar 

  • White DS, Howes BL (1994) Nitrogen incorporation into decomposing litter of Spartina alterniflora. Limnol Oceanogr 39(1):133–140

    Google Scholar 

  • White DS, Howes BL (1994) Translocation, remineralization, and turnover of nitrogen in the roots and rhizomes of Spartina alterniflora (Gramineae). Am J Bot 81:1225–1234

    Google Scholar 

  • Wiegert RG (1986) Modelling spatial and temporal variability in a salt marsh: sensitivity to rates of primary production, tidal migration and microbial degradation. In: Wolfe DA (ed) Estuarine variability. Academic Press Inc., San Diego, California

    Google Scholar 

  • Zar JH (1984) Biostatistical analysis. Prentice-Hall Inc., Englewood Cliffs, New Jersey

    Google Scholar 

Download references

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Communicated by J. P. Grassle, New Brunswick

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Halupa, P.J., Howes, B.L. Effects of tidally mediated litter moisture content on decomposition of Spartina alterniflora and S. patens . Marine Biology 123, 379–391 (1995). https://doi.org/10.1007/BF00353629

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  • DOI: https://doi.org/10.1007/BF00353629

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