Journal of Shellfish Research

Published by: National Shellfisheries Association



Journal of Shellfish Research 30(3):659-669. 2011
doi: http://dx.doi.org/10.2983/035.030.0308

Oyster Shell Dissolution Rates in Estuarine Waters: Effects of pH and Shell Legacy

George G. Waldbusser,1,* Ryan A. Steenson2 and Mark A. Green3

1 College of Oceanic and Atmospheric Sciences, Oregon State University; 104 COAS Administrative Building, Corvallis, OR 97331

2 South Dakota State University, Brookings, SD 57006

3 Division of Natural Sciences, St. Joseph's College of Maine, 278 Whites Bridge Road, Standish, ME 04084

* Corresponding author. E-mail: .

ABSTRACT

Oyster shell is a crucial component of healthy oyster reefs. Shell planting has been a main component of oyster restoration efforts in many habitats and has been carried out on scales from individual and grassroots efforts to multiagency efforts across entire estuaries. However, the cycling and lifetime of the shell that makes up the bulk of an oyster reef has only recently received attention, and most of the work to date has focused on the role of epi- and endobionts on shell degradation. Here we report findings from a laboratory study in which we manipulated pH in a flow-through control system using water from the mesohaline mouth of the Patuxent River to measure dissolution rates of intact oyster shell. Shells from the Eastern oyster (Crassostrea virginica Gmelin 1791) with three different legacies were exposed to 4 levels of pH that encompass a range typical of the mesohaline waters of the Chesapeake Bay (7.2–7.9 on the NBS scale). Mass loss over a 2-wk period was used to measure dissolution rate on 3 shell legacies: fresh, weathered, and dredged. We found that pH and shell legacy had significant effects on shell dissolution rate, with lower pH increasing dissolution rate. Fresh shell had the highest dissolution rate, followed by weathered then dredged shell. Dissolution rates were significantly different among all 4 pH treatments, except between the lowest (7.2) and the next lowest (7.4); however, shells lost mass even under noncorrosive conditions (7.9). We discuss the implications of our findings to ongoing efforts to understand shell budgets and cycling in oyster reef habitat, the interaction of biological and geochemical agents of shell degradation, and the complexity associated with shell carbonate cycling in the unique milieu of the oyster reef.



LITERATURE CITED

Abril, G. & M. Frankignoulle. 2001. Nitrogen—alkalinity interactions in the highly polluted Scheldt basin (Belgium). Water Res. 35:844850. CrossRef, PubMed, CSA
Abril, G., H. Etcheber, B. Delille, M. Frankignoulle & A. V. Borges. 2003. Carbonate dissolution in the turbid and eutrophic Loire estuary. Mar. Ecol. Prog. Ser. 259:129138. CrossRef
Antia, A. N., W. Koeve, G. Fischer, T. Blanz, D. Schulz-Bull, J. Scholten, S. Neuer, K. Kremling, J. Kuss, R. Peinert, D. Hebbeln, U. Bathmann, M. Conte, U. Fehner & B. Zeitzschel. 2001. Basin-wide particulate carbon flux in the Atlantic Ocean: regional export patterns and potential for atmospheric CO2 sequestration. Global Biogeochem. Cycles 15:845862. CrossRef
Aufdenkampe, A. K., E. Mayorga, P. A. Raymond, J. M. Melack, S. C. Doney, S. R. Alin, R. E. Aalto & K. Yoo. 2011. Riverine coupling of biogeochemical cycles between land, oceans, and atmosphere. Front. Ecol. Environ. 9:5360. CrossRef
Beck, M. W., R. D. Brumbaugh, L. Airoldi, A. Carranza, L. D. Coen, C. Crawford, O. Defeo, G. J. Edgar, B. Hancock, M. Kay, H. Lenihan, M. W. Luckenbach, C. L. Toropova & G. Zhang. 2009. Shellfish reefs at risk: a global analysis of problems and solutions. Arlington, VA: The Nature Conservancy. 52 pp.
Bensoussan, N. & J.-P. Gattuso. 2007. Community primary production and calcification in a NW Mediterranean ecosystem dominated by calcareous macroalgae. Mar. Ecol. Prog. Ser. 334:3745. CrossRef
Berner, R. A. 1969. Chemical changes affecting dissolved calcium during bacterial decomposition of fish and clams in sea water. Mar. Geol. 7:253. CrossRef
Borges, A. V. & N. Gypens. 2010. Carbonate chemistry in the coastal zone responds more strongly to eutrophication than to ocean acidification. Limnol. Oceanogr. 55:346353. CrossRef
Burdige, D. J., X. Hu & R. C. Zimmerman. 2010. The widespread occurrence of coupled carbonate dissolution/reprecipitation in surface sediments on the Bahamas Bank. Am. J. Sci. 310: 492521. CrossRef
Burdige, D. J., R. C. Zimmerman & X. Hu. 2008. Rates of carbonate dissolution in permeable sediments estimated from pore-water profiles: the role of sea grasses. Limnol. Oceanogr. 53:549565. CrossRef
Cai, W. J., M. H. Dai & Y. C. Wang. 2006. Air—sea exchange of carbon dioxide in ocean margins: a province-based synthesis. Geophys. Res. Lett. 33. DOI: 10.1029/2006GL026219.
Carriker, M. R., C. P. Swann, R. S. Prezant & C. L. Counts. 1991. Chemical elements in the aragonitic and calcitic microstructural groups of shell of the oyster Crassostrea virginica: a proton probe study. Mar. Biol. 109:287297. CrossRef, CSA
Carver, C. E., I. Theriault & A. L. Mallet. 2010. Infection of cultured Eastern oysters Crassostrea virginica by the boring sponge Cliona celata, with emphasis on sponge life history and mitigation strategies. J. Shellfish Res. 29:905915. BioOne
Cubillas, P., S. Kohler, M. Prieto, C. Chairat & E. H. Oelkers. 2005. Experimental determination of the dissolution rates of calcite, aragonite, and bivalves. Chem. Geol. 216:5977. CrossRef
Davies, D. J., E. N. Powell & R. J. Stanton. 1989. Relative rates of shell dissolution and net sediment accumulation: a commentary: can shell beds form by the gradual accumulation of biogenic debris on the seafloor. Lethaia 22:207212. CrossRef
DeAlteris, J. T. 1988. The geomorphic development of wreck shoal, a subtidal oyster reef of the James River, Virginia. Estuaries 11:240249. CrossRef, CSA
Dickson, A. G., C. L. Sabine & J. R. Christian, editors. 2007. Guide to best practices for ocean CO2 measurements. PICES Spec. Publ. 3: 191 pp.
Driscoll, E. G. 1970. Selective bivalve shell destruction in marine environments: a field study. J. Sediment. Petrol. 40:898.
Edmond, J. M. 1970. High precision determination of titration alkalinity and total carbon dioxide content of sea water by potentiometric titration. Deep-Sea Res. 17:737.
Emerson, S. & M. Bender. 1981. Carbon fluxes at the sediment—water interface of the deep sea: calcium carbonate preservation. J. Mar. Res. 39:139162. CSA
Feely, R. A., S. R. Alin, J. Newton, C. L. Sabine, M. Warner, A. Devol, C. Krembs & C. Maloy. 2010. The combined effects of ocean acidification, mixing, and respiration on pH and carbonate saturation in an urbanized estuary. Estuar. Coast. Shelf Sci. 88:442449. CrossRef
Gattuso, J. P., M. Pichon, B. Delesalle, C. Canon & M. Frankignoulle. 1996. Carbon fluxes in coral reefs. 1. Lagrangian measurement of community metabolism and resulting air—sea CO2 disequilibrium. Mar. Ecol. Prog. Ser. 145:109121. CrossRef, CSA
Gazeau, F., C. Quiblier, J. M. Jansen, J. P. Gattuso, J. J. Middelburg & C. H. R. Heip. 2007. Impact of elevated CO2 on shellfish calcification. Geophys. Res. Lett. 34. DOI: 10.1029/2006GL028554.
Glover, C. P. & S. M. Kidwell. 1993. Influence of organic matrix on the postmortem destruction of molluscan shells. J. Geol. 101:729747. CrossRef
Green, M. A. & R. C. Aller. 1998. Seasonal patterns of carbonate diagenesis in nearshore terrigenous muds: relation to spring phytoplankton bloom and temperature. J. Mar. Res. 56:10971123. CrossRef, CSA
Green, M. A. & R. C. Aller. 2001. Early diagenesis of calcium carbonate in Long Island Sound sediments: benthic fluxes of Ca2+ and minor elements during seasonal periods of net dissolution. J. Mar. Res. 59:769794. CrossRef, CSA
Green, M. A., G. G. Waldbusser, L. Hubazc, E. Cathcart & J. Hall. Carbonate mineral saturation state as the recruitment cue for settling bivalves in marine muds. Estuaries Coasts.
Green, M. A., G. G. Waldbusser, S. L. Reilly, K. Emerson & S. O'Donnell. 2009. Death by dissolution: sediment saturation state as a mortality factor for juvenile bivalves. Limnol. Oceanogr. 54:10371047. CrossRef
Gutierrez, J. L., C. G. Jones, D. L. Strayer & O. O. Iribarne. 2003. Mollusks as ecosystem engineers: the role of shell production in aquatic habitats. Oikos 101:7990. CrossRef, CSA
Gypens, N., A. V. Borges & C. Lancelot. 2009. Effect of eutrophication on air—sea CO(2) fluxes in the coastal southern North Sea: a model study of the past 50 years. Glob. Change Biol. 15:10401056. CrossRef
Hales, B. & S. Emerson. 1997. Evidence in support of first-order dissolution kinetics of calcite in seawater. Earth Planet. Sci. Lett. 148:317327. CrossRef, CSA
Harding, J. M., R. Mann, M. J. Southworth & J. A. Wesson. 2010. Management of the Piankatank River, Virginia, in support of oyster (Crassostrea virginica, Gmelin 1791) fishery repletion. J. Shellfish Res. 29:867888. BioOne
Hargis, W. J. & D. S. Haven. 1999. Chesapeake oyster reefs: Their importance, destruction, and guidelines for restoring them. In: M. W. Luckenbach, R. Mann & J. A. Wesson, eds. Oyster reef habitat restoration: A synopsis and synthesis of approaches. Gloucester, VA: Virginia Institute of Marine Science Press. 372 pp.
Hautmann, M. 2006. Shell mineralogical trends in epifaunal Mesozoic bivalves and their relationship to seawater chemistry and atmospheric carbon dioxide concentration. Facies 52:417433. CrossRef
Hecht, F. 1933. Der Verbleib der organische Substanz der Tiere bei meerischer Einbettung. Senckenb. Biol. 15:165219.
Honjo, S. & J. Erez. 1978. Dissolution rates of calcium carbonate in deep ocean: in situ experiment in North Atlantic Ocean. Earth Planet. Sci. Lett. 40:287300. CrossRef
Hopkins, S. H. 1962. Distribution of species Cliona (boring sponge) on the eastern shore of Virginia in relation to salinity. Chesap. Sci. 2:121124. CrossRef
Hu, X., W. J. Cai, Y. Wang, X. Guo & S. Luo. 2011. Geochemical environments of continental shelf: upper slope sediments in the northern Gulf of Mexico. Palaeogeogr. Palaeoclimatol. Palaeoecol.
Kelly, R. P., M. M. Foley, W. S. Fisher, R. A. Feely, B. S. Halpern, G. G. Waldbusser & M. R. Caldwell. 2011. Mitigating local causes of ocean acidification with existing laws. Science 332:10361037. CrossRef, PubMed
Kidwell, S. M. 2005. Shell composition has no net impact on large-scale evolutionary patterns in mollusks. Science 307:914917. CrossRef, PubMed
Kidwell, S. M. & D. Jablonski. 1983. Taphonomic feedback: ecological consequences of shell accumulation. In: M. J. S. Tevesz & P. L. McCall, editors. Biotic interactions in recent and fossil benthic communities. New York: Plenum Press. pp. 195248.
Kimmel, D. G. & R. I. E. Newell. 2007. The influence of climate variation on Eastern oyster (Crassostrea virginica) juvenile abundance in Chesapeake Bay. Limnol. Oceanogr. 52:959965. CrossRef
Kobluk, D. R. & M. J. Risk. 1977. Calcification of exposed filaments of endolithic algae, micrite envelope formation and sediment production. J. Sediment. Petrol. 47:517528.
Lebrato, M., D. Iglesias-Rodriguez, R. A. Feely, D. Greeley, D. O. B. Jones, N. Suarez-Bosche, R. S. Lampitt, J. E. Cartes, D. R. H. Green & B. Alker. 2010. Global contribution of echinoderms to the marine carbon cycle: CaCO(3) budget and benthic compartments. Ecol. Monogr. 80:441467. CrossRef
Longman, M. W. 1980. Carbonate diagenetic textures from near-surface diagenetic environments. AAPG Bull. Am. Assoc. Petrol. Geologists 64:461487.
Mann, R. & E. N. Powell. 2007. Why oyster restoration goals in the Chesapeake Bay are not and probably cannot be achieved. J. Shellfish Res. 26:905917. BioOne
Mannino, A. & H. R. Harvey. 1999. Lipid composition in particulate and dissolved organic matter in the Delaware Estuary: sources and diagenetic patterns. Geochim. Cosmochim. Acta 63:22192235. CrossRef, CSA
Miller, A. W., A. C. Reynolds, C. Sorbino & G. F. Riedel. 2009. Shellfish face uncertain future in high CO2 world: influence of acidification on oyster larvae calcification and growth in estuaries. PLoS Biol. 4:e5661.
Millero, F. J., T. B. Graham, F. Huang, H. Bustos-Serrano & D. Pierrot. 2006. Dissociation constants of carbonic acid in seawater as a function of salinity and temperature. Mar. Chem. 100:8094. CrossRef
Morse, J. W. 2005. Formation and diagenesis of carbonate sediments. In: F. T. Mackenzie, editor. Sediments, diagenesis, and sedimentary rocks. Oxford: Elsevier-Pergamon. pp. 6786.
Morse, J. W. & R. S. Arvidson. 2002. The dissolution kinetics of major sedimentary carbonate minerals. Earth Sci. Rev. 58:5184. CrossRef
Morse, J. W., R. S. Arvidson & A. Luttge. 2007. Calcium carbonate formation and dissolution. Chem. Rev. 107:342381. CrossRef, PubMed
Morse, J. W. & W. H. Casey. 1988. Ostwald processes and mineral paragenesis in sediments. Am. J. Sci. 288:537560. CrossRef, CSA
Najjar, R. G., C. R. Pyke, M. B. Adams, D. Breitburg, C. Hershner, M. Kemp, R. Howarth, M. R. Mulholland, M. Paolisso, D. Secor, K. Sellner, D. Wardrop & R. Wood. 2010. Potential climate-change impacts on the Chesapeake Bay. Estuar. Coast. Shelf Sci. 86:120. CrossRef
Palma, R. M., G. S. Bressan & D. A. Kietzmann. 2008. Diagenesis of a bioclastic oyster deposit from the Lower Cretaceous (Chachao Formation), Neuquen Basin, Mendoza Province, Argentina. Carbonates Evaporites 23:3949. CrossRef
Pomponi, S. A. & D. W. Meritt. 1990. Distribution and life history of the boring sponge Cliona truitti in the upper Chesapeake Bay. In: K. Rutzler, editor. New perspectives in sponge biology. Washington, DC: Smithsonian Institution Press. pp. 384390.
Pouchou, J. L. & F. Pichoir. 1984. A new model for quantitative X-ray microanalysis. 1. Application to the analysis of homogeneous samples. Recherche Aerospatiale 3:167192.
Powell, E. N., C. E. Brett, K. M. Parsons-Hubbard, W. R. Callender, G. M. Staff, S. E. Walker, A. Raymond & K. A. Ashton-Alcox. 2011a. The relationship of bionts and taphonomic processes in molluscan taphofacies formation on the continental shelf and slope: eight-year trends: Gulf of Mexico and Bahamas. Facies 57:1537. CrossRef
Powell, E. N., J. N. Kraeuter & K. A. Ashton-Alcox. 2006. How long does oyster shell last on an oyster reef? Estuar. Coast. Shelf Sci. 69:531542. CrossRef
Powell, E. N. & J. M. Klinck. 2007. Is oyster shell a sustainable estuarine resource? J. Shellfish Res. 26:181194. BioOne
Powell, E. N., G. M. Staff, W. R. Callender, K. A. Ashton-Alcox, C. E. Brett, K. M. Parsons-Hubbard, S. E. Walker & A. Raymond. 2011b. Taphonomic degradation of molluscan remains during thirteen years on the continental shelf and slope of the northwestern Gulf of Mexico. Palaeogeogr. Palaeoclimatol. Palaeoecol. [in press].
Rosell, D., M. J. Uriz & D. Martin. 1999. Infestation by excavating sponges on the oyster (Ostrea edulis) populations of the Blanes littoral zone (north-western Mediterranean Sea). J. Mar. Biol. Assoc. UK 79:409413. CrossRef
Rude, P. D. & R. C. Aller. 1991. Fluorine mobility during early diagenesis of carbonate sediments: an indicator of mineral transformations. Geochim. Cosmochim. Acta 55:24912509. CrossRef
Salisbury, J., M. A. Green, C. Hunt & J. Campbell. 2008. Coastal acidification by rivers: a threat to shellfish? Eos Trans. AGU 89:513514. CrossRef
Schulte, D. M., R. P. Burke & R. N. Lipcius. 2009. Unprecedented restoration of a native oyster metapopulation. Science 325: 11241128. CrossRef, PubMed
Southworth, M., J. M. Harding, J. A. Wesson & R. Mann. 2010. Oyster (Crassostrea virginica, Gmelin 1791) population dynamics on public reefs in the Great Wicomico River, Virginia, USA. J. Shellfish Res. 29:271290. BioOne
van Heuven, S., D. Pierrot, J. W. B. Rae, E. Lewis & D. W. R. Wallace. 2011. MATLAB Program Developed for CO2 System Calculations. ORNL/CDIAC-105b. Carbon Dioxide Information Analysis Center, Oak Ridge National Laboratory, U.S. Department of Energy, Oak Ridge, Tennessee. DOI: 10.3334/CDIAC/otg.CO2SYS_MATLAB_v1.1.
Waldbusser, G. G., H. Bergschneider & M. A. Green. 2010. Size-dependent pH effect on calcification in post-larval hard clam Mercenaria spp. Mar. Ecol. Prog. Ser. 417:171182. CrossRef
Waldbusser, G. G., E. P. Voigt, H. Bergschneider, M. A. Green & R. I. E. Newell. 2011. Biocalcification in the Eastern oyster (Crassostrea virginica) in relation to long-term trends in Chesapeake Bay pH. Estuaries Coasts 34:221231. CrossRef
Walter, L. M. & J. W. Morse. 1984. Reactive surface-area of skeletal carbonates during dissolution: effect of grain-size. J. Sediment. Petrol. 54:10811090.
Zondervan, I., R. E. Zeebe, B. Rost & U. Riebesell. 2001. Decreasing marine biogenic calcification: a negative feedback on rising atmospheric pCO(2). Global Biogeochem. Cycles 15:507516. CrossRef
Zuschin, M., M. Stachowitsch & R. J. Stanton. 2003. Patterns and processes of shell fragmentation in modern and ancient marine environments. Earth Sci. Rev. 63:3382. CrossRef


 

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