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External and internal factors regulating metabolic rates of an estuarine benthic community

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Summary

The structure and metabolism of a soft-sediment estuarine macrofaunal community were measured over an annual cycle at two depth-contours in mesohaline Chesapeake Bay. Additional data for plankton productivity and respiration, as well as seston and sediment organics are also summarized for these communities. Benthic community respiration ranged from 0.24–3.38 g O2 m-2 d-1, and significant differences were detected between the two depths. Similarly, macroinfaunal standing stocks reached 11.2 and 32.3 g (ash free) m-2 for 3 m and 6 m depth communities, respectively, and both exhibited mid-summer declines in abundance. Inferences drawn from these data facilitated a partitioning of benthic community respiration into macrofaunal and meiofaunal/microbial components with a residual term, much of which could be explained statistically by interactions between these two components. A multi-variate statistical model developed from these data matched benthic respiration measurements within 1–2 S.E. Mass-balances of organic carbon were estimated for water column and benthos at the two depthcontours for early and late summer, as well as for an entire, time-weighted year. These various analyses led to the tentative conclusions that this benthic community was regulated by such internal factors as macrofaunal/meiofaunal grazing and “microbial gardening”, and by external factors such as temperature and predation by nekton. However, it appears that the ultimate control for this community was the supply of energy from organic carbon.

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References

  • Arntz WE (1977) Results and problems of an “unsuccessful” benthos cage experiment (western Baltic). In: BF Keegan, P O' Ceidigh and PJS Boaden (eds) Biology of benthic organisms. London-New York: Pergamon Press, pp 31–34

    Google Scholar 

  • Banse K, Nichols FH, May DR (1971) Oxygen consumption by the seabed. III. On the role of macrofauna at three stations. Vie Milieu Suppl 22:31–52

    Google Scholar 

  • Barsdate RJ, Fenchel T, Prentki RT (1974) Phosphorus cycle of model ecosystems: Significance for decomposer food chains and effects of bacterial grazers. Oikos 25:239–251

    Google Scholar 

  • Bell SS, Coull BC (1978) Field evidence that shrimp predation regulates meiofaina. Oecologia (Berl) 35:141–148

    Google Scholar 

  • Boynton WR, Kemp WM, Osborne CG, Kaumeyer KR (1978) Metabolic characteristics of the water column, benthos and integral community in the vicinity of Calvert Cliffs, Chesapeake Bay. Ref. No. UMCEES 78-139-CBL, Chesapeake Biological Laboratory, Solomons, MD. pp 67

    Google Scholar 

  • Briggs KB, Tenore KR, Hanson RB (1979) The role of macrofauna in detrital utilization by the polychaete, Nereis succinea. J exp Mar Biol Ecol 36:225–234

    Google Scholar 

  • Carey AG Jr (1967) Energetics of the benthos of Long Island Sound. I. Oxygen utilization of sediment. Bull. Bingham Oceanogr Coll 19:136–144

    Google Scholar 

  • Cargo DG, Biggs RB (1969) Comments on hydrographic phenomena in the Chesapeake Bay, with special reference to the Calvert Cliffs nuclear power plant. Ref. No. NRI 69-106, Chesapeake Biological Laboratory, Solomons, MD pp 12

    Google Scholar 

  • Connell JH (1975) Some mechanisms producing structure in natural communities: A model and evidence from field experiments. In: Ecology and evolution of communities. ML Cody and JM Diamond (eds). Cambridge: Harvard Univ. Press, pp 460–490

    Google Scholar 

  • Ehrlich PR, Birch LC (1967) The “balance of nature” and “population control”. Amer Nat 101:97–107

    Google Scholar 

  • Fenchel T, (1969) The ecology of marine meiobenthos IV. Structure and function of the benthic ecosystem, its chemical and physical factors and the microfauna communities with special reference to the ciliate protozoa. Ophelia 6:1–182

    Google Scholar 

  • Fenchel T (1970) Studies on the decomposition of organic detritus derived from the turtle grass, Thalassis testudinum. Limnol Oceanogr 15:14–20

    Google Scholar 

  • Fenchel T, Harrison P (1976) The significance of bacterial grazing and mineral cycling for the decomposition of particulate detritus. In: JM Anderson, A Macfadyen (eds) The role of terrestrial and aquatic organisms in decomposition process. Oxford: Blackwell Sci Publ, pp 285–300

    Google Scholar 

  • Gaarder T, Gran HH (1927) Investigations of the production of plankton in the Oslo Fjord. Rapp. et Proc.-Verb., Cons Internat Explor Mer 42:1–48

    Google Scholar 

  • Gerlach SA (1971) On the importance of marine meiofauna for benthic communities. Oecologia (Berl)6:176–190

    Google Scholar 

  • Gerlach SA (1978) Food chain relationships in subtidal silty sand marine sediments and the role of meiofauna in stimulating bacterial productivity. Oecologia (Berl) 33:55–69

    Google Scholar 

  • Hairston NG, Smith FE, Slobodkin LB (1960) Community structure, population control, and competition. Amer Nat 94:421–425

    Google Scholar 

  • Hale SS (1975) The role of benthic communities in the nitrogen and phosphorus cycles of an estuary. In: FG Howell, JB Gentry MH Smith (eds) Mineral cycling in southeastern ecosystems. Springfield, VA: National Techn Info Serv (CONF-740513) pp 291–308

    Google Scholar 

  • Hall CAS, Moll R (1975) Methods of assessing aquatic primary production. In: A. Leith, R Whitaker (eds) Primary production of the biosphere. Springer, Berlin Heidelberg New York, pp 19–53

    Google Scholar 

  • Hargrave BT (1969a) Similarity of oxygen uptake by benthic communities. Limnol Oceanogr 14:801–805

    Google Scholar 

  • Hargrave BT (1969b) Epibenthic algal production and community respiration in the sediments of Marion Lake. J Fish Res Bd Canada 26:2004–2026

    Google Scholar 

  • Hargrave BT (1970) The effect of a deposit-feeding amphipod on the metabolism of benthic microflora. Limnol Oceanogr 15:21–30

    Google Scholar 

  • Hargrave BT (1973) Coupling carbon flow through some pelagic and benthic communities. J Fish Res Board Can 30:1317–1326

    Google Scholar 

  • Harris RP (1972) Seasonal changes in the meiofauna population of an intertidal sand beach. J Mar Biol Ass UK 52:389–403

    Google Scholar 

  • Heinle DR, Taft JL, D'Elia CF, Wilson JS, Cole-Jones M, Vivian AB (1980) Historical review of water quality and climatic data in Chesapeake Bay with emphasis on effects of enrichment. Publ No. 84, Chesapeake Research Consortium, Annapolis, MD

  • Holland AF, Mountford NK, Mihursky JA (1977) Temporal variation in upper bay mesohaline benthic communities: I. The 9-m mud habitat. Chesapeake Sci 18:370–378

    Google Scholar 

  • Holland AF, Mountford NK, Hiegel M, Kaumeyer K, Cargo D, Mihursky JA (1978) Results of benthic studies at Calvert Cliffs. Ref. No. CC-78-2 Martin Marietta Corp., Baltimore, MD. and Ref. No. 78-165-CBL Chesapeake Biological Laboratory, Solomons, MD. pp 120

    Google Scholar 

  • Holland AF, Mountford NK, Hiegel MH, Kaumeyer KR, Mihursky JA (1980) The influence of predation on infaunal abundance in upper Chesapeake Bay. Marine Biol 57:221–235

    Google Scholar 

  • Hylleberg J (1975) Selective feeding by Abarenicola pacifica with notes on Abarenicola vagabunda and a concept of gardening in lugworms. Ophelia 14:113–137

    Google Scholar 

  • Jenkins MC, Boynton WR (1978) Selected structural and functional aspects of estuarine benthic communities. Ref. No. 78-85-CBL. Chesapeake Biological Laboratory, Solomons, MD

    Google Scholar 

  • Kemp WM, Boynton WR (1980) Influence of biological and physical factors on dissolved oxygen dynamics in an estuarine system: Implications for measurement of community metabolism. Estuarine Coastal Mar Sci 11:407–431

    Google Scholar 

  • Kennedy VS, Mihursky JA (1972) Effects of temperature on the respiratory metabolism of three Chesapeake Bay bivalves. Chespeake Sci 13:1–22

    Google Scholar 

  • Kofoed LH (1975) The feeding biology of Hydrobia ventrosa. I. The assimilation of different components of the food. J exp mar Biol Ecol 19:233–241

    Google Scholar 

  • Mann KH (1972) Macrophyte production and detritus food chains in coastal waters. Mem 1st Ital Idrobiol Suppl 29:353–383

    Google Scholar 

  • McIntyre AD (1964) Meiobenthos of sublittoral muds. J Mar Biol Ass UK 44:665–674

    Google Scholar 

  • Menzel DE, Vaccaro RF (1964) The measurement of dissolved organic and particulate carbon in seawater. Limnol Oceanogr 9:138–142

    Google Scholar 

  • Mihursky JA (ed) (1978) Ecological effects of nuclear steam electric station operations on estuarine systems. Sixth progress report to U.S. Energy Research and Development Agency. Ref. No. 77-27-CBL. Chesapeake Biological Laboratory, Solomons, MD

    Google Scholar 

  • Mihursky JA, Homer ML, Holland AF (1979) Trophic relationships of demersal fish communities in the Calvert Cliffs, Maryland, Chesapeake Bay area. Estuarine Research Federation Conf. Jekyll Is., GA. (Abstract)

  • Mountford NK, Holland AF, Mihursky JA (1977) Identification and description of macrobenthic communities in the Calvert Cliffs region of the Chesapeake Bay. Chesapeake Sci 18:360–369

    Google Scholar 

  • Murdoch WW (1966) “Community structure, population control, and competition” — A critique. Amer Nat 100:219–226

    Google Scholar 

  • Newcombe CL, Horne WA (1938) Oxygen-poor waters of the Chesapeake Bay Science 88:80–81

    Google Scholar 

  • Newcombe CL, Horne WA, Shephard BB (1939) Studies on the physics and chemistry of estuarine waters in Chesapeake Bay. J Mar Res 11:87–116

    Google Scholar 

  • Newell RC (1965) The role of detritus in the nutrition of two marine deposit-feeders, the prosobranch Hydrobia ulvae and the bivalve Macoma balthica. Proc Zool Soc, London 144:25–45

    Google Scholar 

  • Nichols FH (1975) Dynamics and energetics of three deposit-feeding benthic invertebrate populations in Puget Sound, Washington. Ecol Monogr 45:57–82

    Google Scholar 

  • Nixon SW (1980) Remineralization and nutrient cycling in coastal marine ecosystems. In: B Neilson, LE Cronin (eds) Nutrient enrichment in estuaries. Humana Press (in press)

  • Nixon SW, Kelly JR, Furnas BN, Oviatt CA (1980) Phosphorus regeneration and metabolism of coastal marine bottom communities. In: KR Tenore, BC Coull (eds) Marine benthic dynamics. Columbia: Univ South Carolina Press (in press)

    Google Scholar 

  • Orth RJ (1977) The importance of sediment stability in seagrass communities. In: BC Coull (ed) Ecology of marine benthos. Columbia: Univ South Carolina Press, pp 281–300

    Google Scholar 

  • Osborne CG, Kaumeyer KR, Keefe CW, Boynton WR, Kemp WM (1979) Community metabolism and nutrient dynamics of the Patuxent Estuary interacting with Chalk Point Power Plant. Ref. No. UMCEES 79-8-CBL, Chesapeake Biological Laboratory, Solomons, MD

    Google Scholar 

  • Pamatmat MM (1968) Ecology and metabolism of a benthic community on an intertidal sandflat. Int Revue ges Hydrobiol 53:211–298

    Google Scholar 

  • Pamatmat MM (1977) Benthic community metabolism: A review and assessment of present status and outlook. In: BC Coull (ed) Ecology of marine benthos. Columbia: Univ South Carolina Press, pp 89–111

    Google Scholar 

  • Pritchard DW (1967) Observations of circulation in coastal plain estuaries. In: GH Lauff (ed) Estuaries, Publ. No. 83: Washington: Amer Assoc Adv Sci, pp 37–44

    Google Scholar 

  • Reise K (1977) Predator exclusion experiments in an intertidal mud flat. Holgolander wiss Meeresunters 30:263–271

    Google Scholar 

  • Rhoads DC (1974) Organism-sediment relations on the muddy sea floor. Oceanogr Mar Biol Ann Rev 12:263–300

    Google Scholar 

  • Rhoads DC, McCall PL, Yingst JY (1978) Disturbance and production on the estuarine seafloor. Amer Scientist 66:577–586

    Google Scholar 

  • Ryther JH (1956) The measurement of primary production. Limnol Oceanogr 1:72–84

    Google Scholar 

  • Sanders HL (1958) Benthic studies in Buzzards Bay. I. Animal-sediment relationships. Limnol Oceanogr 3:245–258

    Google Scholar 

  • Slobodkin LG, Smith FE, Hairston NG (1967) Regulation in terrestrial ecosystems, and the implied balance of nature. Amer Nat 101:109–124

    Google Scholar 

  • Smith KL (1971) Structural and functional aspects of a sublittoral community. Ph.D. Thesis. Athens: Univ Georgia, pp 194

    Google Scholar 

  • Smith KL (1973) Respiration of a sublittoral community. Ecology 54:1065–1075

    Google Scholar 

  • Smith KL (1978) Benthic community respiration in the N.W. Atlantic Ocean: in situ measurements from 40 to 5,200 m. Mar Biol 47:337–347

    Google Scholar 

  • Smith KL, Rowe GT, Nichols JA (1973) Benthic community respiration near the Woods Hole sewage outfall. Estuarine Coastal Mar Sci 1:65–70

    Google Scholar 

  • Stanier RY, Duodoroff M, Adelberg EA (1970) The microbial world (Third Ed.). Englewood Cliffs, NJ: Prentice-Hall

    Google Scholar 

  • Strickland JDH, Parsons TR (1972) A practical handbook of seawater analysis. Bull. 167 (2nd edition). Ottawa: Fish Res Bd Canada

    Google Scholar 

  • Tenore KR, Tietjen JH, Lee JJ (1977) Effect of meiofauna on incorporation of aged eelgrass, Zostera marina, detritus by the polychaete, Nephthys incisa. J Fish Res Bd Can 34:563–567

    Google Scholar 

  • Tietjen JH (1969) The ecology of shallow water meiofauna in two New England estuaries. Oecologia (Berl) 2:251–291

    Google Scholar 

  • Virnstein RW (1977) The importance of predation by crabs and fishes on benthic infauna in Chesapeake Bay Ecology 58:1199–1217

    Google Scholar 

  • Virnstein RW (1978) Predator caging experiments in soft sediments: caution advised. In: ML Wiley (ed) Estuarine interactions. New York-San Francisco-London: Academic Press, pp 261–273

    Google Scholar 

  • Virnstein RW (1979) Predation on estuarine infauna: Response patterns of component species. Estuaries 2:69–86

    Google Scholar 

  • Wiegert RG, Owen DF (1971) Trophic structure, available resources and population density in terrestrial versus aquatic eco-systems. J Theor Biol 30:69–81

    Google Scholar 

  • Yetka JE, Wiebe WJ (1974) Ecological application of antibiotics as respiratory inhibitors of bacterial populations. Appl Microbiol 28:1033–1039

    Google Scholar 

  • Young DK, Young MW (1977) Community structure of the macrobenthos associated with seagrass of the Indian River Estuary, Florida. In: BC Coull (ed) Ecology of marine benthos. Columbia: Univ South Carolina Press, pp 359–381

    Google Scholar 

  • Young DK, Young MW (1978) Regulation of species densities of seagrass-associated macrobenthos: Evidence from field experiments in the Indian River estuary, Florida. J Mar Res 36:569–593

    Google Scholar 

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Authors and Affiliations

  1. Center for Environmental and Estuarine Studies, University of Maryland, College Park, Maryland, USA

    W. Michael Kemp

  2. Horn Point Environmental Laboratories, Box 775, 21613, Cambridge, MD, USA

    Walter R. Boynton

  3. Chesapeake Biological Laboratory, Box 38, 20688, Solomons, MD, USA

    W. Michael Kemp & Walter R. Boynton

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  1. W. Michael Kemp
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  2. Walter R. Boynton
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Contribution No. HPEL-1206, USA

Supported by grants with the Maryland Department of Natural Resources (PS-72-02(77-78)), J.A. Mihursky, Coordinating Principal Investigator

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Kemp, W.M., Boynton, W.R. External and internal factors regulating metabolic rates of an estuarine benthic community. Oecologia 51, 19–27 (1981). https://doi.org/10.1007/BF00344646

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  • DOI: https://doi.org/10.1007/BF00344646

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