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Modelling the Spatial Distribution of Oyster (Crassostrea virginica) Biodeposits Settling from Suspended Aquaculture

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Abstract

Oysters in suspended aquaculture filter out particulates from the water column and release pseudofeces and feces (collectively called biodeposits) back to the water column. These biodeposits consist of dense assemblages of labile organic matter that quickly settle to the sediment surface. To properly quantify the environmental effects of biodeposition from suspended aquaculture, it is necessary to determine where the biodeposits settle. An analytical/numerical model was developed for suspended aquaculture systems to predict the spatial distribution of biodeposits; input parameters include water depth, tidal elevation, biodeposit settling rate, and wind and tidally driven current velocity. The biodeposit model was validated in three shallow Cape Cod, Massachusetts, estuaries characterized by low-energy hydrodynamics. For each site, model-predicted carbon deposition was regressed against measured carbon remineralization (determined from sediment oxygen uptake) obtained from intact sediment cores collected along a gradient of predicted carbon deposition. Results showed that in summer, nearly all carbon deposited was remineralized but that the fraction of deposited carbon that is remineralized decreases considerably with declining temperatures in the fall. The simple analytical/numerical model developed and validated in this study provides a tool for commercial oyster growers and environmental managers to assess the effect of organic matter deposition by suspended oyster aquaculture over the growing season. This approach can be applied in shallow depositional coastal systems.

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References

  • Archer, A., J. Reitsma, and D. Murphy. 2014. A comparison of bottom and floating gear for growing American oysters (Crassostrea virginica) in southeastern Massachusetts. Woods Hole Sea Grant Cape Cod Coop. Ext.

  • Berner, R. A. 1980. Early Diagenesis: A Theoretical Approach. Princeton: Princeton University Press.

    Book  Google Scholar 

  • Buttner, J., G. Flimlin, and D. Webster. 2008. Marine Aquaculture Species for the Northeast. 103–2008. College Park, Maryland: Northeastern Regional Aquaculture Center.

  • Callier, M., A. Weise, C. McKindsey, and G. Desrosiers. 2006. Sedimentation rates in a suspended mussel farm (Great-Entry Lagoon, Canada): Biodeposit production and dispersion. Marine Ecology Progress Series 322: 129–141. https://doi.org/10.3354/meps322129.

    Article  CAS  Google Scholar 

  • Chamberlain, J. 2001. Impacts of biodeposits from suspended mussel (Mytilus edulis L.) culture on the surrounding surficial sediments. ICES Journal of Marine Science 58: 411–416. https://doi.org/10.1006/jmsc.2000.1037.

    Article  Google Scholar 

  • Comeau, L.A., A.L. Mallet, C.E. Carver, and T. Guyondet. 2014. Impact of high-density suspended oyster culture on benthic sediment characteristics. Aquaculture Engineering 58: 95–102. https://doi.org/10.1016/j.aquaeng.2013.12.004.

    Article  Google Scholar 

  • Cromey, C.J., T.D. Nickell, and K.D. Black. 2002. DEPOMOD—modelling the deposition and biological effects of waste solids from marine cage farms. Aquaculture 214: 211–239. https://doi.org/10.1016/S0044-8486(02)00368-X.

    Article  Google Scholar 

  • Doiron, S. 2008. Reference Manual for Oyster Aquaculturists. Fredericton, New Brunswick: New Brunswick Department of Agriculture, Fisheries and Aquaculture.

  • Everett, R.A., G.M. Ruiz, and J.T. Carlton. 1995. Effect of oyster mariculture on submerged aquatic vegetation: An experimental test in a Pacific Northwest estuary. Marine Ecology Progress Series 125: 205–217.

    Article  Google Scholar 

  • FAO. 2020. The State of World Fisheries and Aquaculture 2020. Rome: Sustainability in action.

    Google Scholar 

  • Forrest, B.M., and R.G. Creese. 2006. Benthic impacts of intertidal oyster culture, with consideration of taxonomic sufficiency. Environmental Monitoring and Assessment 112: 159–176.

    Article  Google Scholar 

  • Foster-Smith, R.L. 1975. The effect of concentration of suspension on the filtration rates and pseudofaecal production for Mytilus edulis L., Cerastoderma edule (L.) and Venerupis pullastra (Montagu), Journal of Experimental Marine Biology and Ecology 17.1: 1–22. https://doi.org/10.1016/0022-0981(75)90075-1

  • Gaurier, B., G. Germain, Y. Kervella, J. Davourie, F. Cayocca, and P. Lesueur. 2011. Experimental and numerical characterization of an oyster farm impact on the flow. European Journal of Mechanics-B/Fluids 30: 513–525. https://doi.org/10.1016/j.euromechflu.2011.05.001.

    Article  Google Scholar 

  • Giles, H., N. Broekhuizen, K.R. Bryan, and C.A. Pilditch. 2009. Modelling the dispersal of biodeposits from mussel farms: The importance of simulating biodeposit erosion and decay. Aquaculture 291: 168–178. https://doi.org/10.1016/j.aquaculture.2009.03.010.

    Article  Google Scholar 

  • Giles, H., and C. Pilditch. 2006. Effects of mussel (Perna canaliculus) biodeposit decomposition on benthic respiration and nutrient fluxes. Marine Biology 150: 261–271. https://doi.org/10.1007/s00227-006-0348-7.

    Article  CAS  Google Scholar 

  • Giles, H., and C. Pilditch. 2004. Effects of diet on sinking rates and erosion thresholds of mussel Perna canaliculus biodeposits. Marine Ecology Progress Series 282: 205–219. https://doi.org/10.3354/meps282205.

    Article  Google Scholar 

  • Grant, J., P. Cranford, B. Hargrave, M. Carreau, B. Schofield, S. Armsworthy, V. Burdett-Coutts, and D. Ibarra. 2005. A model of aquaculture biodeposition for multiple estuaries and field validation at blue mussel (Mytilus edulis) culture sites in eastern Canada. Canadian Journal of Fisheries and Aquatic Sciences 62: 1271–1285. https://doi.org/10.1139/f05-033.

    Article  Google Scholar 

  • Grenz, C., M. Hermin, D. Baudinet, and R. Daumas. 1990. In situ biochemical and bacterial variation of sediments enriched with mussel biodeposits. Hydrobiologia 207: 153–160. https://doi.org/10.1007/BF00041452.

    Article  CAS  Google Scholar 

  • Hartstein, N.D., and C.L. Stevens. 2005. Deposition beneath long-line mussel farms. Aquaculture Engineering 33: 192–213. https://doi.org/10.1016/j.aquaeng.2005.01.002.

    Article  Google Scholar 

  • Hatakeyama, Y., T. Kawahata, M. Fujibayashi, O. Nishimura, and T. Sakamaki. 2021. Sources and oxygen consumption of particulate organic matter settling in oyster aquaculture farms: Insights from analysis of fatty acid composition. Estuarine, Coastal and Shelf Science 254. https://doi.org/10.1016/j.ecss.2021.107328

  • Haven, D.S., and R. Morales-Alamo. 1966. Aspects of biodeposition by oysters and other invertebrate filter feeders. Limnology and Oceanography 11: 487–498. https://doi.org/10.4319/lo.1966.11.4.0487.

    Article  Google Scholar 

  • Haven, D.S., and R. Morales-Alamo. 1972. Biodeposition as a factor in sedimentation of fine suspended solids in estuaries. Geological Society of America Memoir 133: 121–130. https://doi.org/10.1130/MEM133-p121.

    Article  Google Scholar 

  • Higgins, C.B., K. Stephenson, and B.L. Brown. 2011. Nutrient bioassimilation capacity of aquacultured oysters: Quantification of an ecosystem service. Journal of Environmental Quality 40: 271–277. https://doi.org/10.2134/jeq2010.0203.

    Article  CAS  Google Scholar 

  • Higgins, C., C. Tobias, M. Piehler, A. Smyth, R. Dame, K. Stephenson, and B. Brown. 2013. Effect of aquacultured oyster biodeposition on sediment N2 production in Chesapeake Bay. Marine Ecology Progress Series 473: 7–27. https://doi.org/10.3354/meps10062.

    Article  CAS  Google Scholar 

  • Hoellein, T.J., and C.B. Zarnoch. 2014. Effect of eastern oysters (Crassostrea virginica) on sediment carbon and nitrogen dynamics in an urban estuary. Ecological Applications 24: 271–286. https://doi.org/10.1890/12-1798.1.

    Article  Google Scholar 

  • Kaspar, H.F., P.A. Gillespie, I.C. Boyer, and A.L. MacKenzie. 1985. Kaspar, H. F., P. A. Gillespie, I. C. Boyer, and A. L. MacKenzie. Effects of mussel aquaculture on the nitrogen cycle and benthic communities in Kenepuru Sound, Marlborough Sounds. New Zealand Marine Biology 85: 127–136.

    CAS  Google Scholar 

  • Kellogg, M.L., A.R. Smyth, M.W. Luckenbach, et al. 2014. Use of oysters to mitigate eutrophication in coastal waters. Estuarine, Coastal and Shelf Science 151: 156–168. https://doi.org/10.1016/j.ecss.2014.09.025.

    Article  CAS  Google Scholar 

  • Kervella, Y., G. Germain, B. Gaurier, J.-V. Facq, F. Cayocca, and P. Lesueur. 2010. Experimental study of the near-field impact of an oyster table on the flow. European Journal of Mechanics-B/Fluids 29: 32–42. https://doi.org/10.1016/j.euromechflu.2009.09.002.

    Article  Google Scholar 

  • Khalil, K., M. Raimonet, A. Laverman, C. Yan, F. Andrieux-Loyer, E. Voiller, B. Deflandre, O. Ragueneau, and C. Rabouille. 2013. Spatial and temporal variability of sediment organic matter recycling in two temperate eutrophicated estuaries. Aquatic Geochemistry 19: 517–542.

    Article  CAS  Google Scholar 

  • Labrie, M.S. 2021. Quantifying Impacts of Suspended Oyster Aquaculture on Nitrogen Cycling in a Southeastern Massachusetts Coastal Embayment. PhD Dissertation: University of Massachusetts, Dartmouth, MA, USA.

  • Li, J., Y.P. Wang, J. Du, F. Luo, P. Xin, J. Gao, B. Shi, X. Chen, and S. Gao. 2021a. Effects of Meretrix meretrix on sediment thresholds of erosion and deposition on an intertidal flat. Ecohydrology and Hydrobiology 21: 129–141. https://doi.org/10.1016/j.ecohyd.2020.07.002.

    Article  CAS  Google Scholar 

  • Li, J., X. Chen, I. Townend, B. Shi, J. Du, J. Gao, X. Chuai, Z. Gong, and Y.P. Wang. 2021b. A comparison study on the sediment flocculation process between a bare tidal flat and a clam aquaculture mudflat: The important role of sediment concentration and biological processes. Marine Geology. https://doi.org/10.1016/j.margeo.2021.106443.

    Article  Google Scholar 

  • McKindsey, C.W., M. Lecuona, M. Huot, and A.M. Weise. 2009. Biodeposit production and benthic loading by farmed mussels and associated tunicate epifauna in Prince Edward Island. Aquaculture 295: 44–51. https://doi.org/10.1016/j.aquaculture.2009.06.022.

    Article  Google Scholar 

  • Newell, R.I.E., T.R. Fisher, R.R. Holyoke, and J.C. Cornwell. 2005. Influence of Eastern Oysters on Nitrogen and Phosphorus Regeneration in Chesapeake Bay, USA, p. 93–120. In R.F. Dame and S. Olenin [eds.], The Comparative Roles of Suspension-Feeders in Ecosystems. Springer-Verlag.

  • Newell, R.I.E., and C.J. Langdon. 1996. Mechanisms and physiology of larval and adult feeding. p. 185–230. In V. S. Kennedy, R. I. E. Newell, and A. Eble [eds.], The eastern oyster, Crassostrea virginica. Maryland Sea Grant Publication.

  • Nixon, S.W., C.A. Oviatt, J. Garber, and V. Lee. 1976. Diel metabolism and nutrient dynamics in a salt marsh embayment. Marine Ecology Progress Series 141: 263–274. https://doi.org/10.2307/1936187.

    Google Scholar 

  • Ottmann, F., and J.M. Sornin. 1982. Relationship between marine bottom elevation and various types of marine culture. Atlantica 5: 88–89.

    Google Scholar 

  • Parsons, T.R., Y. Maita, and C. Lalli. 1989. Manual of Chemical and Biological Methods for Seawater Analysis. Pergamon Press, p. 173.

  • Rudnick, D.T., and C.A. Oviatt. 1986. Seasonal lags between organic carbon deposition and mineralization in marine sediments. Journal of Marine Research 44: 815–837. https://doi.org/10.1357/002224086788401594.

    Article  CAS  Google Scholar 

  • Shaw, K.C., B.L. Howes, and D. Schlezinger. 2018. Macroalgal composition and accumulation in New England estuaries. Journal of Environmental Management 206: 246–254.

    Article  CAS  Google Scholar 

  • Shi, B., P.D. Pratolongo, Y. Du, J. Li, S.L. Yang, J. Wu, K. Xu, and Y.P. Wang. 2020. Influence of macrobenthos (Meretrix meretrix Linnaeus) on erosion‐accretion processes in intertidal flats: A case study from a cultivation zone. Journal of Geophysical Research: Biogeosciences 125: p.e2019JG005345.

  • Tenore, K.R., and W.M. Dunstan. 1973. Comparison of feeding and biodeposition of three bivalves at different food levels. Marine Biology 21 (3): 190–195.

    Article  Google Scholar 

  • Testa, J., D. Brady, J. Cornwell, M. Owens, L. Sanford, C. Newell, S. Suttles, and R. Newell. 2015. Modeling the impact of floating oyster (Crassostrea virginica) aquaculture on sediment-water nutrient and oxygen fluxes. Aquaculture Environment Interactions 7: 205–222. https://doi.org/10.3354/aei00151.

    Article  Google Scholar 

  • Thamdrup, B., J.W. Hansen, and B.B. Jørgensen. 1998. Temperature dependence of aerobic respiration in a coastal sediment. FEMS Microbiology Ecology 25 (2): 189–200. https://doi.org/10.1111/j.1574-6941.1998.tb00472.x.

    Article  CAS  Google Scholar 

  • Town of Mashpee Sewer Commission. 2015. Final recommended plan/final environmental impact report. Comprehensive Wastewater Management Plan, Town of Mashpee. Hyannis: GHD Inc.

  • Town of Orleans Water Quality and Wastewater Planning. 2016. Amended Comprehensive Wastewater Management Plan – Preliminary Draft. Pocasset: AECOM Technical Services Inc.

    Google Scholar 

  • U.S. Department of Agriculture. 2019. 2017 Census of Agriculture: Census of Aquaculture (2018). (AC-17-SS-2). https://www.nass.usda.gov/Publications/AgCensus/2017/Online_Resources/Aquaculture/Aqua.pdf

  • Weise, A.M., C.J. Cromey, M.D. Callier, P. Archambault, J. Chamberlain, and C.W. McKindsey. 2009. Shellfish-DEPOMOD: Modelling the biodeposition from suspended shellfish aquaculture and assessing benthic effects. Aquaculture 288: 239–253. https://doi.org/10.1016/j.aquaculture.2008.12.001.

    Article  Google Scholar 

  • Widdows, J., M.D. Brinsley, P.N. Salkeld, and M. Elliott. 1998. Use of annular flumes to determine the influence of current velocity and bivalves on material flux at the sediment-water interface. Estuaries 21: 552–559. https://doi.org/10.2307/1353294.

    Article  Google Scholar 

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Acknowledgements

The authors thank the United States Environmental Protection Agency Southeast New England Program and the Towns of Orleans and Falmouth for supporting this work. We gratefully acknowledge Science Wares Inc. for maintaining the oyster arrays and their assistance determining oyster survival and growth, and the Westport Director of Marine Services, Chris Leonard, and the Westport River Watershed Alliance who assisted in gear construction and deployments in Cockeast Pond. In addition, we thank the Falmouth Marine and Environmental Services Director, Chuck Martinsen, for supplying the oysters and gear for the Bournes Pond site. Finally, we thank D.R. Schlezinger, J. Benson, S. Horvet, A. Unruh, and N. Uline of the Coastal Systems Program at SMAST-UMD. We sincerely appreciate the helpful comments of the two anonymous reviewers whose recommendations significantly improved this manuscript.

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Correspondence to Micheline S. Labrie.

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Labrie, M.S., Sundermeyer, M.A. & Howes, B.L. Modelling the Spatial Distribution of Oyster (Crassostrea virginica) Biodeposits Settling from Suspended Aquaculture. Estuaries and Coasts 45, 2690–2709 (2022). https://doi.org/10.1007/s12237-022-01096-4

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