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Ammonium excretion by gelationous zooplankton and their contribution to the ammonium requirements of microplankton in Chesapeake Bay

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Abstract

Ammonium excretion rates of recently collected specimens of gelatinous zooplankton, the scyphomedusan Chrysaora quinquecirrha DeSor and the etenophore Mnemiopsis leidyi A. Agassiz, were correlated with body mass and water temperature in measurements made from April to October 1989 and 1990. Rates ranged between 3.5 and 5.0 μg atoms NH +4 -N (g dry wt)-1h-1 for C. quinquecirrha and 3.0 to 4.9 μg atoms NH +4 -N (g dry wt)-1h-1 for M. leidyi. Excretion rate equations and in situ data on the size distributions and biomasses of gelatinous zooplankters and water temperature were used to estimate the contribution of ammonium by medusae and ctenophores to mesohaline Chesapeake Bay waters on several dates during April to October 1989 and 1990. We then compared the estimated contributions to direct measurements of 15NH +4 uptake by microplankton. The maximum estimated regeneration by gelatinous zooplankton was 5.8 μg atoms NH +4 -N m-3h-1 at night in August 1990, when medusae biomass was greatest. This represents about 4% of the ammonium required by the microplankton. During the daytime on all dates, less than 1% of the ammonium required by microplanktion was supplied by gelatinous zooplankton. Therefore, gelatinous zooplankton appear to play a minor role in the ammonium cycle of Chesapeake Bay.

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Literature cited

  • Bidigare, R. R. (1983). Nitrogen excretion by marine zooplankton. In: Carpenter, E. J., Capone, D. G. (eds.) Nitrogen in the marine environment. Academic Press, New York, p. 385–410

    Google Scholar 

  • Biggs, D. C. (1977). Respiration and ammonium excretion by open ocean gelatinous zooplankton. Limnol. Oceanogr. 22: 108–117

    Google Scholar 

  • Biggs, D. C., Bidigare, R. R., Smith, D. E. (1981). Population density of macrozooplankton: in situ estimation in oceanic surface waters. Biol. Oceanogr. (N.Y.) 1: 157–173

    Google Scholar 

  • Biggs, D. C., Smith, D. E., Bidigare, R. R., Johnson, M. A. (1984). In situ estimation of the population density of gelatinous planktivores in Gulf of Mexico surface waters. In: Flemming, N. C. (ed.) Divers, submersibles, and marine science. Memorial Univ. New foundland, Occ. Pap. Biol. 9: 17–34

  • Carpenter, E. J., Ramson, C. C., Watson, S. W. (1972). Utilization of urea by some marine phytoplankters. Limnol. Oceanogr. 17: 265–269

    Google Scholar 

  • Cochlan, W. P., Harrison, P. J., Denman, K. L. (1991). Diel periodicity of nitrogen uptake by marine phytoplankton in nitrate-rich environments. Limnol. Oceanogr. 36: 1689–1700

    Google Scholar 

  • Costello, J. (1991). Complete carbon and nitrogen budgets for the hydromedusa Cladonema californicum (Anthomedusa: Cladonemidae). Mar. Biol. 108: 119–128

    Google Scholar 

  • Feigenbaum, D., Kelly, M. (1984). Changes in the lower Chesapeake Bay food chain in presence of the sea nettle Chrysaora quinquecirrha (Scyphomedusa). Mar. Ecol. Prog. Ser. 19: 39–47

    Google Scholar 

  • Glibert, P. M. (1982). Regional studies of daily, seasonal and size fraction variability in ammonium remineralization. Mar. Biol. 70: 209–222

    Google Scholar 

  • Glibert, P. M., Garside, C. (1992). Diel variability in nitrogenous nutrient uptake by phytoplankton in the Chesapeake Bay plume. J. Plankton Res. 14: 271–288

    Google Scholar 

  • Hamburger, K., Mohlenberg, F., Randlov, A., Riisgard, H. U. (1983). Size, oxygen consumption and growth in the mussel Mytilus edulis. Mar. Biol. 75: 303–306

    Google Scholar 

  • Harrison, W. G. (1978). Experimental measurements of nitrogen remineralization in coastal waters. Limnol. Oceanogr. 23: 684–694

    Google Scholar 

  • Ikeda, T. (1985). Metabolic retes of epipelagic marine zooplankton as a function of body mass and temperature. Mar. Biol. 85: 1–11

    Google Scholar 

  • Kremer, P. (1975). Nitrogen regeneration by the ctenophore Mnemiopsis leidyi. In: Howell, F. G., Howell, J. B., Smith, M. H. (eds.) Mineral cycling in southeastern ecosystems. ERDA Sumposium Series (Conf-740513), Kingston, Rhode-Island, p. 279–290

  • Kremer, P. (1976). Excretion and body composition of the ctenophore Mnemiopsis leidyi (A. Agassiz): comparisons and consequences. Proc. 10th Eur. mar. Biol. Symp. 2: 351–356 [Persoone, G., Jaspers, E. (eds.). Universa Press, Wetteren, Belgiuml

    Google Scholar 

  • Kremer, P. (1977). Respiration and excretion by the ctenophore Mnemiopsis leidyi. Mar. Biol. 44: 43–50

    Google Scholar 

  • Kremer, P. (1982). Effect of food availability on the metabolism of the ctenophore Mnemiopsis mccradyi. Mar. Biol. 71: 149–156

    Google Scholar 

  • Kremer, P., Canino, M. F., Gilmer, R. W. (1986). Metabolism of epipelagic ctenophores. Mar. Biol. 90: 403–412

    Google Scholar 

  • La Roche, J. (1983). Ammonium regeneration: its contribution to phytoplankton nitrogen requirements in a eutrophic environment. Mar. Biol. 75: 231–240

    Google Scholar 

  • Larson, R. J. (1987). Respiration and carbon turnover rates of medusae from the NE Pacific. Comp. Biochem. Physiol. A 87: 93–100

    Google Scholar 

  • Malej, A. (1991). Rates of metabolism of jellyfish as related to body weight, chemical composition and temperature. In: Jellyfish blooms in the Mediterranean. Proc. 2nd Workshop on Jellyfish in the Mediterranean Sea. United Nations Environmental Programme, Mediterranean Action Plan Technical Reports 47: 253–257

  • Malone, T. C., Crocker, L. H., Pike, S. E., Wendler, B. W. (1988). Influences of river flow on the dynamics of phytoplankton production in a partially stratified estuary. Mar. Ecol. Prog. Ser. 48: 235–249

    Google Scholar 

  • Malone, T. C., Kemp, W. M., Ducklow, H. W., Boynton, W. H., Tuttle, W. H., Jonas, R. H. (1986). Lateral variation in the production and fate of phytoplankton in a partially stratified estuary. Mar. Ecol. Prog. Ser. 32: 149–160

    Google Scholar 

  • Matsakis, S. (1992). Ammonia excretion rate of Clytia spp. hydromedusae (Cnidaria, Thecata): effects of individual dry weight, temperature and food availability. Mar. Ecol. Prog. Ser. 87: 55–63

    Google Scholar 

  • McCarthy, J. J., Taylor, W. H., Taft, J. L. (1977). Nitrogenous nutrition of the plankton in the Chesapeake Bay. 1. Nutrient availability and phytoplankton preferences. Limnol. Oceanogr. 22: 996–1011

    Google Scholar 

  • Morand, P., Carre, C. H., Biggs, D. C. (1987). Feeding and metabolism of the jellyfish Pelagia noctiluca (Scyphomedusae, Semaeostomae). J. Plankton Res. 9: 651–665

    Google Scholar 

  • Nemazie, D. A. (1991). Ammonium excretion by gelatinous zooplankton and its role in the regeneration of nitrogen in Chesapeake Bay. M. S. Thesis, University of Maryland, College Park, Maryland

    Google Scholar 

  • Olson, M. M. (1987). Zooplankton. In: Heck, K. L. Jr. (ed.) Ecological studies in the middle reach of Chesapeake Bay. 23. Lecture notes on coastal and estuarine studies. Springer-Verlag, New York, p. 38–81

    Google Scholar 

  • Park, Y. C., Carpenter, E. J. (1987). Ammonium regeneration and biomass of macrozooplankton and ctenophores in Great South Bay, New York. Estuaries 10: 316–320

    Google Scholar 

  • Parsons, T. R., Maita, Y., Lalli, C. M. (1985). A manual of chemical and biological methods for seawater analysis. Pergamon Press, New York

    Google Scholar 

  • Purcell, J. E. (1988). Quantification of Mnemiopsis leidyi (Ctenophora, Lobata) from formalin-preserved plankton samples. Mar. Ecol. Prog. Ser. 45: 197–200

    Google Scholar 

  • Purcell, J. E. (1992). Effects of predation by the scyphomedusan Chrysaora quinquecirrha on zooplankton populations in Cheasapeake Bay, U.S.A. Mar. Ecol. Prog. Ser. 87: 65–76

    Google Scholar 

  • Purcell, J. E., Cresswell, F. P., Cargo, D. G., Kennedy, V. S. (1991). Differential ingestion and digestion of bivalve larvae by the scyphozoan Chrysaora quinquecirrha and the ctenophore Mnemiopsis leidyi. Biol. Bull. mar. biol. Lab., Woods Hole 180: 103–111

    Google Scholar 

  • Purcell, J. E., Kremer, P. (1983). Feeding and metabolism of the siphonophore Sphaeronectes gracilis. J. Plankton Res. 5: 95–106

    Google Scholar 

  • Schneider, G. (1989). The common jellyfish Aurelia aurita: standing stock, excretion and nutrient regeneration in the Kiel Bight, Western Baltic. Mar. Biol. 100: 507–514

    Google Scholar 

  • Szyper, J. P. (1981). Short-term starvation effects on nitrogen and phosphorous excretion by the chaetognath Sagitta enflata. Estuar. cstl shelf Sci. 13: 691–700

    Google Scholar 

  • White, J. R. (1991). Seasonal studies on zooplankton dynamics in the mesohaline Chesapeake Bay. Ph. D. Thesis, University of Maryland, College Park, Maryland

    Google Scholar 

  • Youngbluth, M. J., Kremer, P., Bailey, T. G., Jacoby, C. A. (1988). Chemical composition, metabolic rates and feeding behavior of the midwater ctenophore Bathocyroe fosteri. Mar. Biol. 98: 87–94

    Google Scholar 

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Communicated by J. P. Grassle, New Brunswick

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Nemazie, D.A., Purcell, J.E. & Glibert, P.M. Ammonium excretion by gelationous zooplankton and their contribution to the ammonium requirements of microplankton in Chesapeake Bay. Marine Biology 116, 451–458 (1993). https://doi.org/10.1007/BF00350062

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