Estuaries and Coasts

, Volume 40, Issue 1, pp 173–186 | Cite as

The Carbonate Chemistry of the “Fattening Line,” Willapa Bay, 2011–2014

  • Burke Hales
  • Andy Suhrbier
  • George G. Waldbusser
  • Richard A. Feely
  • Jan A. Newton
Article

Abstract

Willapa Bay has received a great deal of attention in the context of rising atmospheric CO2 and the concomitant effects of changes in bay carbonate chemistry, referred to as ocean acidification, and the potential effects on the bay’s naturalized Pacific oyster (Crassostrea gigas) population and iconic oyster farming industry. Competing environmental stressors, historical variability in the oyster settlement record, and the absence of adequate historical observations of bay-water carbonate chemistry all conspire to cast confusion regarding ocean acidification as the culprit for recent failures in oyster larval settlement. We present the first measurements of the aqueous CO2 partial pressure (PCO2) and the total dissolved carbonic acid (TCO2) at the “fattening line,” a location in the bay that has been previously identified as optimal for both larval oyster retention and growth, and collocated with a long historical time series of larval settlement. Samples were collected from early 2011 through late 2014. These measurements allow the first rigorous characterization of Willapa Bay aragonite mineral saturation state (Ωar), which has been shown to be of leading importance in determining the initial shell formation and growth of larval Crassostrea gigas. Observations show that the bay is usually below Ωar levels that have been associated with poor oyster hatchery production and with chronic effects noted in experimental work. Bay water only briefly rises to favorable Ωar levels and does so out of phase with optimal thermal conditions for spawning. Thermal and carbonate conditions are thus coincidentally favorable for early larval development for only a few weeks at a time each year. The limited concurrent exceedance of thermal and Ωar thresholds suggests the likelihood of high variability in settlement success, as seen in the historical record; however, estimates of the impact of elevated atmospheric CO2 suggest that pre-industrial Ωar conditions were more persistently favorable for larval development and more broadly coincident with thermal optima.

Keywords

Estuarine carbonate chemistry Oyster settlement Ocean acidification 

References

  1. Banas, N.S., B.M. Hickey, P. MacCready, and J.A. Newton. 2004. Dynamics of Willapa Bay, Washington: A highly unsteady, partially mixed estuary. Journal of Physical Oceanography 34: 2413–2427.CrossRefGoogle Scholar
  2. Banas, N.S., and B.M. Hickey. 2005. Mapping exchange and residence time in a model of Willapa Bay, Washington, a branching, macrotidal estuary. Journal Geophysical Research C 110: C11011. doi:10.1029/2005JC002950.CrossRefGoogle Scholar
  3. Banas, N.S., B.M. Hickey, J.A. Newton, and J.L. Ruesink. 2007. Tidal exchange, bivalve grazing, and patterns of primary production in Willapa Bay, Washington. Marine Ecology Progress Series 341: 123–139.CrossRefGoogle Scholar
  4. Bandstra, L., B. Hales, and T. Takahashi. 2006. High-frequency measurement of seawater total carbon dioxide. Marine Chemistry. doi:10.1016/j.marchem.2005.10.009. Google Scholar
  5. Barton, A., G.G. Waldbusser, R.A. Feely, S.B. Weisberg, J.A. Newton, B. Hales, S. Cudd, B. Eudeline, C. Langdon, I. Jefferds, T. King, and K. Mclaughlin. 2015. Impacts of coastal acidification on the Pacific Northwest shellfish industry and adaptation strategies implemented in response. Oceanography 28(2): 146–159. doi:10.5670/oceanog.2015.38.CrossRefGoogle Scholar
  6. Barton, A., B. Hales, G. Waldbusser, C. Langdon, and R. Feely. 2012. The Pacific oyster, Crassostrea gigas, shows negative correlation to naturally elevated carbon dioxide levels: Implications for near-term ocean acidification impacts. Limnology and Oceanography 57: 698–710. doi:10.4319/lo.2012.57.3.0698. CrossRefGoogle Scholar
  7. Bochenek, E.A., J.M. Klinck, E.N. Powell, and E.E. Hofmann. 2001. A biochemically based model of the growth and development of Crassostrea gigas larvae. Journal of Shellfish Research 20: 243–265.Google Scholar
  8. Borges, A.V., and N. Gypens. 2010. Carbonate chemistry in the coastal zone responds more strongly to eutrophication than to ocean acidification. Limnology and Oceanography 55: 346–353.CrossRefGoogle Scholar
  9. Cai, W.-J.X. Hu, W. Huang, M.C. Murrell, J.C. Lehrter, S.E. Lohrenz, W.-C. Chou, W. Zhai, J.T. Hollibaugh, Y. Wang, P. Zhao, X. Guo, K. Gundersen, M. Dai, and G.-C. Gong. 2011. Acidification of subsurface coastal waters enhanced by eutrophication. Nature Geoscience 4: 766–770. http://www.nature.com/ngeo/journal/v4/n11/abs/ngeo1297.html#supplementary-information
  10. Chapman, W.M., and G.D. Esveldt. 1943. The spawning and setting of the Pacific oyster (Ostrea gigas Thunberg) in the state of Washington in 1942. In Biological report, 40. Seattle, WA: Washington Department of Fisheries.Google Scholar
  11. Dickson, A., C. L. Sabine, and J. R. Christian (Eds.) 2007. Guide to best practices for ocean CO2 measurements. PICES Special Publication 3, 191 pp.Google Scholar
  12. Dickson, A.G. 1990. Thermodynamics of the dissociation of boric acid in synthetic sea water from 273.15 to 298.15 K. Deep Sea Research 37: 755–766.CrossRefGoogle Scholar
  13. Doney, S.C., V.J. Fabry, R.A. Feely, and J.A. Kleypas. 2009. Ocean Acidification: The other CO2 problem. Annual Review of Marine Science 1: 169–192.CrossRefGoogle Scholar
  14. Dumbauld, B. R., and L. M. McCoy, 2015. The effect of oyster aquaculture on seagrass (Zostera marina) at the estuarine landscape scale in Willapa Bay, Washington (USA). Aquaculture Environment Interactions, in revision.Google Scholar
  15. Dumbauld, B.R., B.E. Kauffmann, A.C. Trimble, and J.L. Ruesink. 2011. The Willapa Bay oyster reserves in Washington State: Fishery collapse, creating a sustainable replacement, and the potential for habitat conservation and restoration. Journal of Shellfish Research 30: 71–83.CrossRefGoogle Scholar
  16. Ekstrom, J., L. Suatoni, S. Cooley, L. Pendleton, G.G. Waldbusser, J. Cinner, J. Ritter, C. Langdon, R. van Hooidonk, D. Gledhill, K. Wellman, M. Beck, L. Brander, D. Rittschof, C. Doherty, P. Edwards, and R. Portela. 2015. Vulnerability and adaptation of US shellfisheries to ocean acidification. Nature Climate Change 5: 207–214. doi:10.1038/nclimate2508.
  17. Elston, R.A., H. Hasegawa, K.L. Humphrey, I.K. Polyak, and C.C. Hase. 2008. Re-emergence of Vibrio tubiashii in bivalve shellfish aquaculture: severity, environmental drivers, geographic extent and management. Diseases of Aquatic Organisms 82: 119–134.CrossRefGoogle Scholar
  18. Emmett, R., R. Llansó, J. Newton, R. Thom, M. Hornberger, C. Morgan, C. Levings, A. Copping, and P. Fishman. 1999. Geographic signatures of North American west coast estuaries. Estuaries 23: 765–792.CrossRefGoogle Scholar
  19. Feely, R.A., C.L. Sabine, K. Lee, W. Berelson, J. Kleypas, V.J. Fabry, and F.J. Millero. 2004. Impact of anthropogenic CO2 on the CaCO3 system in the oceans. Science 305(5682): 362–366. doi:10.1126/science.1097329,.CrossRefGoogle Scholar
  20. Feely, R.A., C.L. Sabine, J.M. Hernandez-Ayon, D. Ianson, and B. Hales. 2008. Evidence for upwelling of corrosive ‘acidified’ water onto the continental shelf. Science 320: 1490–1492.CrossRefGoogle Scholar
  21. Feely, R.A., S.R. Alin, J. Newton, C.L. Sabine, M. Warner, A. Devol, C. Krembs, and C. Maloy. 2010. The combined effects of ocean acidification, mixing, and respiration on pH and carbonate saturation in an urbanized estuary. Estuarine, Coastal. Shelf Science 88: 442–449. doi:10.1016/j.ecss.2010.05.004,.CrossRefGoogle Scholar
  22. Feely, R.A., T. Klinger, J.A. Newton, and M. Chadsey, 2012. Scientific Summary of Ocean Acidification in Washington State Marine Waters. NOAA OAR Special Report, 170 pp.
  23. Feely, R.A., S.R. Alin, B. Carter, N. Bednarsek, B. Hales, F. Chan, T. Hill, B. Gaylord, E. Sanford, R. Byrne, C. Sabine, and D. Greeley. 2016. Chemical and biological impacts of ocean acidification along the west coast of North America.  Estuarine, Coastal, and Shelf Science, revision submitted.Google Scholar
  24. Hales, B., T. Takahashi, and L. Bandstra. 2005. Atmospheric CO2 uptake by a coastal upwelling system. Global Biogeochemical Cycles 19. doi:10.1029/2004GB002295.
  25. Hales, B., D. Chipman, and T. Takahashi. 2004. High-frequency measurement of partial pressure and total concentration of carbon dioxide in seawater using microporous hydrophobic membrane contactors. Limnology and Oceanography: Methods 2: 356–364.CrossRefGoogle Scholar
  26. Harris, K.E., M.D. DeGrandpre, and B. Hales. 2013. Aragonite saturation states in a coastal upwelling zone. Geophysical Research Letters. doi:10.1002/grl.50460. Google Scholar
  27. Hauri, C., N. Gruber, M. Vogt, S.C. Doney, R.A. Feely, Z. Lachkar, A. Leinweber, A.M.P. McDonnell, M. Munnich, and G.-K. Plattner. 2013. Spatiotemporal variabiliry and long-term trends of ocean acidification in the California Current System. Biogeosciences 10: 193–216. doi:10.5194/bg-10-193-2013.
  28. Hickey, B.M., and N.S. Banas. 2003. Oceanography of the U. S. Pacific Northwest coastal ocean and estuaries with application to coastal ecology. Estuaries 26: 1010–1031.CrossRefGoogle Scholar
  29. Huyer, A., R. Pillsbury, and R. Smith. 1978. Seasonal variation of the alongshore velocity field over the continental shelf off Oregon. Limnology and Oceanography 20: 90–95.CrossRefGoogle Scholar
  30. Huyer, A., E. Sobey, and R. Smith. 1979. The spring transition in currents over the Oregon continental shelf. Journal of Geophysical Research 84: 6995–7011.CrossRefGoogle Scholar
  31. Kelly, R.P., M.M. Foley, W.S. Fisher, R.A. Feely, B.S. Halpern, G.G. Waldbusser, and M.R. Caldwell. 2011. Mitigating local causes of ocean acidification with existing laws. Science Policy Forum 332. doi:10.1126/science.1203815.
  32. Kennedy, V.S. 1996. Biology of larvae and spat. In The Eastern Oyster, Crassostrea virginica, eds. V.S. Kennedy, R.I.E. Newell, and A. Eble, 371–421. College Park, MD: Maryland Sea Grant.Google Scholar
  33. Kimmel, D.G., and R.I.E. Newell. 2007. The influence of climate variation on eastern oyster (Crassostrea virginica) juvenile abundance in Chesapeake Bay. Limnology and Oceanography 52: 959–965.CrossRefGoogle Scholar
  34. Mann, R., E. Burreson, and P.K. Baker. 1991. The decline of the Virginia oyster fishery in Chesapeake Bay: considerations for introduction of a non-endemic species, Crassostrea gigas (Thunberg). Journal of Shellfish Research 10(2): 379–388.Google Scholar
  35. Millero, F.J. 2010. Carbonate constants for estuarine waters. Marine and Freshwater Research 61: 139–142.CrossRefGoogle Scholar
  36. Millero, F.J. 1995. Thermodynamics of the carbon dioxide system in the oceans. Geochimica et Cosmochimica Acta 59: 661–677.CrossRefGoogle Scholar
  37. Mucci, A. 1983. The solubility of calcite and aragonite in seawater at various salinities, temperatures, and one atmosphere total pressure. American Journal of Science 283: 780–799.CrossRefGoogle Scholar
  38. Nelson, J. 1903. Report of Biologist: Part I, Experimental studies in oyster propagation. pp 333–369, in Ann. Rep. N.J. Agric. Exp. Sta. 1902. New Brunswick, NJ.Google Scholar
  39. Newton, J.A., and R.A. Horner. 2003. Use of phytoplankton species indicators to track the origin of phytoplankton blooms, Washington. Estuaries 26: 1071–1078.CrossRefGoogle Scholar
  40. Portner, H.O. 2008. Effects of ocean acidification on marine ecosystems. Marine Ecology Progress Series 373: 203–217. doi:10.334/meps07868.
  41. Reum, J.C.P., S.R. Alin, R.A. Feely, J. Newton, M. Warner, and P. McElhany. 2014. Seasonal carbonate chemistry covariation with temperature, oxygen, and salinity in a fjord estuary: Implications for the design of ocean acidification experiments. PloS One 9(2): e89619. doi:10.1371/journal.pone.0089619. CrossRefGoogle Scholar
  42. Reinsch, C.J. 1967. Smoothing spline functions. Numerische Mathematik 29: 177–283.CrossRefGoogle Scholar
  43. Ruesink, J.L., G.C. Roegner, B.R. Dumbauld, J.A. Newton, and D.A. Armstrong. 2003. Contributions of coastal and watershed energy sources to secondary production in a northeastern Pacific estuary. Estuaries 26: 1079–1093.CrossRefGoogle Scholar
  44. Ruesink, J.L., S. Yang, and A.C. Trimble. 2015. Variability in carbon availability and eelgrass (Zostera marina) biometrics along an estuarine gradient in Willapa Bay, WA, USA. Estuaries and Coasts 38:1908-1917. doi:10.1007/s12237-014-9933-z.
  45. Rumrill, S.S. 1990. Natural mortality of marine invertebrate larvae. Ophelia 32: 163–198.CrossRefGoogle Scholar
  46. Sabine, C.L., and R.A. Feely. 2007. In Greenhouse Gas Sinks, eds. D. Reay, N. Hewitt, J. Grace, K. Smith. Oxfordshire, UK: CABI.Google Scholar
  47. Sabine, C.L., R.A. Feely, N. Gruber, R.M. Key, K. Lee, J.L. Bullister, R. Wanninkhof, C.S. Wong, D.W.R. Wallace, B. Tilbrook, F.J. Millero, T.-H. Peng, A. Kozyr, T. Ono, and A.F. Rios. 2004. The oceanic sink for anthropogenic CO2. Science 305(5682): 367–371. doi:10.1126/science.1097403,.CrossRefGoogle Scholar
  48. Salisbury, J., M. Green, C. Hunt, and J. Campbell. 2008. Coastal acidification by rivers: A threat to shellfish? Eos 89: 513–514.CrossRefGoogle Scholar
  49. Sherwood, C.R., and J.S. Creager. 1990. Sedimentary geology of the Columbia River estuary. Progress in Oceanography 25: 15–79.CrossRefGoogle Scholar
  50. Soetaert, K., A.F. Hofmann, J.J. Middelburg, F.J.R. Meysman, and J. Greenwood. 2007. The effect of biogeochemical processes on pH. Marine Chemistry 105: 30–51.CrossRefGoogle Scholar
  51. Steele, E.N. 1964. The immigrant oyster (Ostrea gigas) now known as the Pacific oyster, 179. Olympia, WA: Warren’s Quick Print.Google Scholar
  52. Sunda, W.G., and W.J. Cai. 2012. Eutrophication Induced CO2-Acidification of Subsurface Coastal Waters: Interactive Effects of Temperature, Salinity, and Atmospheric PCO2. Environmental Science & Technology 46: 10651–10659.CrossRefGoogle Scholar
  53. Takahashi, T., S.C. Sutherland, C. Sweeney, A. Poisson, N. Metzl, B. Tilbrook, N. Bates, R. Wanninkhof, R.A. Feely, C. Sabine, J. Olafson, and Y. Nojiri. 2002. Global sea–air CO2 flux based on climatological surface ocean pCO2, and seasonal biological and temperature effects.  Deep-Sea Res II 49: 1601–1622.Google Scholar
  54. Takahashi, T., et al. 2009. Climatological mean and decadal change in surface ocean pCO2, and net sea-air CO2 flux over the global oceans. Deep Sea Research. doi:10.1016/j.dsr2.2008.12.009. Google Scholar
  55. Takahashi, T., S.C. Sutherland, D.W. Chipman, J.G. Goddard, C. Ho, T. Newberger, C. Sweeney, and D.R. Munro. 2014. Climatological distributions of pH, pCO2, total CO2, alkalinity and CaCO3 saturation in the global surface ocean, and temporal changes at selected locations. Marine Chemistry 164: 95–125.CrossRefGoogle Scholar
  56. Waldbusser, G.G., B. Hales, C.J. Langdon, B.A. Haley, P. Schrader, E.L. Brunner, M.W. Gray, C.A. Miller, and I. Gimenez. 2015a. Experimental Evidence for Saturation State Impacts on Early Larval Bivalves. Nature Climate Change. doi:10.1038/NCLIMATE2479.Google Scholar
  57. Waldbusser, G.G., B. Hales, C.J. Langdon, B.A. Haley, P. Schrader, E.L. Brunner, M.W. Gray, C.A. Miller, I. Gimenez, and G. Hutchinson. 2015b. Ocean acidification has multiple modes of action on bivalve larvae. PloS One 10(6): e0128376. doi:10.1371/journal.pone.0128376.CrossRefGoogle Scholar
  58. Waldbusser, G.G., and J.E. Salisbury. 2014. Ocean Acidification in the Coastal Zone from an Organism’s Perspective: Multiple System Parameters, Frequency Domains, and Habitats. Annual Review of Marine Science 6: 221–247.CrossRefGoogle Scholar
  59. Waldbusser, G.G., E.P. Voigt, H. Bergschneider, M.A. Green, and R.I. Newell. 2011. Biocalcification in the eastern oyster (Crassostrea virginica) in relation to long-term trends in Chesapeake Bay pH. Estuaries and Coasts 34: 221–231.CrossRefGoogle Scholar
  60. Waldbusser, G.G., E. Brunner, B. Haley, B. Hales, F. Prahl, and C. Langdon. 2013. A developmental and energetic basis linking larval oyster shell formation to ocean acidification. Geophysical Research Letters. doi:10.1002/grl.50449. Google Scholar
  61. Wallace, R.B., H. Baumann, J.S. Grear, R.C. Aller, and C.J. Gobler. 2014. Coastal ocean acidification: The other eutrophication problem. Estuarine, Coastal and Shelf Science 148: 1–13. doi:10.1016/j.ecss.2014.05.027.
  62. Washington State Blue Ribbon Panel on Ocean Acidification, 2012. Ocean Acidification: From Knowledge to Action, Washington State’s Strategic Response. H. Adelsman and L. Whitely Binder (eds). Olympia, Washington: Washington Department of Ecology. Publication no. 12-01-015.Google Scholar
  63. Wheatcroft, R.A., M.A. Goni, J.A. Hatten, G.B. Pasternack, and J.A. Warrick. 2010.  The role of effective discharge in the ocean delivery of particulate organic carbon bysmall, mountainous river systems. Limnology and Oceanography 55: 161–171.Google Scholar

Copyright information

© Coastal and Estuarine Research Federation 2016

Authors and Affiliations

  • Burke Hales
    • 1
  • Andy Suhrbier
    • 2
  • George G. Waldbusser
    • 1
  • Richard A. Feely
    • 3
  • Jan A. Newton
    • 4
  1. 1.College of Earth, Ocean and Atmospheric SciencesOregon State UniversityCorvallisUSA
  2. 2.Pacific Shellfish InstituteOlympiaUSA
  3. 3.NOAA Pacific Marine Environmental LaboratorySeattleUSA
  4. 4.University of Washington Applied Physics LaboratorySeattleUSA

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