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Evidence for stratigraphy in molluscan death assemblages preserved in seagrass beds: St. Croix, U.S. Virgin Islands

Published online by Cambridge University Press:  21 January 2018

Kelsey M. Arkle
Affiliation:
Department of Geology, University of Cincinnati, Cincinnati, Ohio 45221-0013, U.S.A. E-mail: kelseyarkle@augustana.edu.
Arnold I. Miller
Affiliation:
Department of Geology, University of Cincinnati, Cincinnati, Ohio 45221-0013, U.S.A. E-mail: kelseyarkle@augustana.edu.

Abstract

Death assemblages that occupy the upper tens of centimeters of sediment in shallow-marine settings are often subject to extensive mixing, thereby limiting their usefulness in assessing environmentally mediated compositional changes through time in the local biota. Here, we provide evidence that dense, Thalassia-rich seagrass beds preserve a stratigraphic record of biotic variation because their dense root–rhizome mats inhibit mixing. We sampled benthic mollusk assemblages at seven localities in Thalassia-rich beds around St. Croix, USVI, collecting three separate sediment intervals of ~13 cm each to a total depth of ~40 cm below the sediment–water interface, and found evidence that sedimentary intervals preserved compositional stratigraphy. Further, some localities displayed systematic, directional changes down-core. An examination of interval-to-interval changes in composition revealed that compositional variation was unique from locality to locality rather than reflecting coordinated, island-wide transitions. In general, however, relative abundances of epifaunal gastropods and small lucinid bivalves tended to decrease with depth below the sediment–water interface. Quantitative comparisons of life-to-death assemblages from each successive sedimentary interval demonstrated that the shallowest death assemblages were typically more similar to the life assemblages than were deeper assemblages, suggesting that deeper intervals provide records of earlier community states.

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Articles
Copyright
Copyright © 2018 The Paleontological Society. All rights reserved 

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References

Literature Cited

Abbott, R. T., and Morris, P. A.. 1995. A field guide to shells of the Atlantic and Gulf Coasts and the West Indies (The Peterson Field Guide Series). Houghton Mifflin, Boston.Google Scholar
Albano, P. G., Filippova, N., Steger, J., Kaufman, D. S., Tomašových, A., Stachowitsch, M., and Zuschin, M.. 2016. Oil platforms in the Persian (Arabian) Gulf: living and death assemblages reveal no effects. Continental Shelf Research 121:2134.Google Scholar
Bray, J. R., and Curtis, J. T.. 1957. An ordination of the upland forest communities of southern Wisconsin. Ecological Monographs 27:325349.Google Scholar
Brenchley, G. A. 1982. Mechanisms of spatial competition in marine soft-bottom communities. Journal of Experimental Marine Biology and Ecology 60:1733.Google Scholar
Brewster-Wingard, G. L., and Ishman, S. E.. 1999. Historical trends in salinity and substrate in central Florida Bay: a paleoecological reconstruction using modern analogue data. Estuaries 22:369383.Google Scholar
Burdige, D. J., and Zimmerman, R. C.. 2002. Impact of seagrass density on carbonate dissolution in Bahamian sediments. Limnology and Oceanography 47:17511763.Google Scholar
Burke, R. B., Adey, W. H., and MacIntyre, I. G.. 1989. Overview of the Holocene history, architecture, and structural components of Tague reef and lagoon. In D.K. Hubbard, ed. Terrestrial and marine geology of St. Croix, U.S. Virgin Islands. West Indies Laboratory Special Publication 8:105109.Google Scholar
Burney, D. A., James, H. F., Burney, L. P., Olson, S. L., Kikuchi, W., Wagner, W. L., Burney, M., McCloskey, D., Kikuchi, D., and Grady, F. V.. 2001. Fossil evidence for a diverse biota from Kaua’i and its transformation since human arrival. Ecological Monographs 71:615641.Google Scholar
Clarke, K. R. 1993. Non-parametric multivariate analyses of changes in community structure. Australian Journal of Ecology 18:117143.CrossRefGoogle Scholar
Clarke, K. R., and Warwick, R. M.. 2001. Change in marine communities: an approach to statistical analysis and interpretation, 2nd ed. PRIMER-E, Plymouth, U.K.Google Scholar
Cruz-Palacios, V., and van Tussenbroek, B. I.. 2005. Simulation of hurricane-like disturbances on a Caribbean seagrass bed. Journal of Experimental Marine Biology and Ecology 324:4460.Google Scholar
Davies, D. J., Powell, E. N., and Stanton, R. J. Jr. 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 sea floor? Lethaia 22:207212.CrossRefGoogle Scholar
Edgar, G., and Samson, C.. 2004. Catastrophic decline in mollusc diversity in eastern Tasmania and its concurrence with shellfish fisheries. Conservation Biology 18:15791588.Google Scholar
Edinger, E. N., Pandolfi, J. M., and Kelley, R. A.. 2001. Community structure of Quaternary coral reefs compared with Recent life and death assemblages. Paleobiology 27:669694.Google Scholar
Edmunds, P. J. 2002. Long-term dynamics of coral reefs in St. John, US Virgin Islands. Coral Reefs 21:357367.CrossRefGoogle Scholar
Erthal, F., Kotzian, C. B., and Simões, M. G.. 2011. Fidelity of molluscan assemblages from the Touro Passo formation (Pleistocene–Holocene), southern Brazil: taphonomy as a tool for discovering natural baselines for freshwater communities. Palaios 26:433446.CrossRefGoogle Scholar
Espinosa, M., De Francesco, C., and Isla, F.. 2003. Paleoenvironmental reconstruction of Holocene coastal deposits from the southeastern Buenos Aires Province, Argentina. Journal of Paleolimnology 29:4960.Google Scholar
Ferguson, C. A. 2008. Nutrient pollution and the molluscan death record: use of mollusc shells to diagnose environmental change. Journal of Coastal Research 24:250259.Google Scholar
Ferguson, C. A., and Miller, A. I.. 2007. A sea change in Smuggler’s Cove? Detection of decadal-scale compositional transitions in the subfossil record. Palaeogeography, Palaeoclimatology, Palaeoecology 254:418429.Google Scholar
Feser, K. M., and Miller, A. I.. 2014. Temporal dynamics of shallow seagrass-associated molluscan assemblages in St. Croix, US Virgin Islands: toward the calibration of taphonomic inertia. Palaios 29:218230.Google Scholar
Flessa, K. W., and Kowalewski, M.. 1994. Shell survival and time-averaging in nearshore and shelf environments: estimates from the radiocarbon literature. Lethaia 27:153165.CrossRefGoogle Scholar
Frenzel, P., and Boomer, I.. 2005. The use of ostracods from marginal marine, brackish waters as bioindicators of modern and Quaternary environmental change. Palaeogeography, Palaeoclimatology, Palaeoecology 225:6892.Google Scholar
Gilinsky, N. L., and Bennington, J. B.. 1994. Estimating numbers of whole individuals from collections of body parts: a taphonomic limitation of the paleontological record. Paleobiology 20:245258.Google Scholar
Ginsburg, R. N., and Lowenstam, H. A.. 1958. The influence of marine bottom communities on the depositional environment of sediments. Journal of Geology 66:310318.Google Scholar
Goodfriend, G. A. 1992. The use of land snail shells in paleoenvironmental reconstruction. Quaternary Science Reviews 11:665685.Google Scholar
Greenstein, B. J., and Pandolfi, J. M.. 1997. Preservation of community structure in modern reef coral life and death assemblages of the Florida Keys: implications for the Quaternary fossil record of coral reefs. Bulletin of Marine Science 61:431452.Google Scholar
Harrison, P. G. 1987. Natural expansion and experimental manipulation of seagrass (Zostera spp.) abundance and the response of infaunal invertebrates. Estuarine, Coastal and Shelf Science 24:799812.Google Scholar
Holland, A. F. 1985. Long-term variation of macrobenthos in a mesohaline region of Chesapeake Bay. Estuaries 8:93113.Google Scholar
Hurlbert, S. H. 1971. The nonconcept of species diversity: a critique and alternative parameters. Ecology 52:577586.Google Scholar
Kennett, J. P. 1982. Marine geology. Prentice-Hall, Englewood Cliffs, N.J.Google Scholar
Kidwell, S. M. 2007. Discordance between living and death assemblages as evidence for anthropogenic ecological change. Proceedings of the National Academy of Sciences USA 104:1770117706.Google Scholar
Kidwell, S. M. 2008. Ecological fidelity of open marine molluscan death assemblages: effects of post-mortem transportation, shelf health, and taphonomic inertia. Lethaia 41:199217.Google Scholar
Kidwell, S. M., and Bosence, D. W. J.. 1991. Taphonomy and time-averaging of marine shelly faunas. Pp. 115209 in P. A. Allison, and D. E. G. Briggs, eds. Taphonomy: releasing the data locked in the fossil record. Plenum, New York.Google Scholar
Kidwell, S. M., and Flessa, K. W.. 1996. The quality of the fossil record: populations, species, and communities. Annual Review of Earth and Planetary Sciences 24:433464.Google Scholar
Kosnik, M. A., Hua, Q., Kaufman, D. S., and Wüst, R. A.. 2009. Taphonomic bias and time-averaging in tropical molluscan death assemblages: differential shell half-lives in great barrier reef sediment. Paleobiology 35:565586.Google Scholar
Kosnik, M. A., Kaufman, D. S., and Hua, Q.. 2013. Radiocarbon-calibrated multiple amino acid geochronology of Holocene molluscs from Bramble and Rib Reefs (Great Barrier Reef, Australia). Quaternary Geochronology 16:7386.Google Scholar
Kowalewski, M. 1990. A hermeneutic analysis of the shell-drilling gastropod predation on mollusks in the Korytnica clays (middle Miocene; Holy Cross Mountains, Central Poland). Acta Geologica Polonica 40:183214.Google Scholar
Kowalewski, M., Goodfriend, G. A., and Flessa, K. W.. 1998. High-resolution estimates of temporal mixing within shell beds: the evils and virtues of time-averaging. Paleobiology 24:287304.Google Scholar
Kowalewski, M., Serrano, G. E. A., Flessa, K. W., and Goodfriend, G. A.. 2000. Dead delta’s former productivity: two trillion shells at the mouth of the Colorado River. Geology 28:10591062.Google Scholar
Mikkelsen, P. M., and Bieler, R.. 2008. Seashells of Southern Florida: living marine mollusks of the Florida Keys and adjacent regions. Princeton University Press, Princeton, N.J.Google Scholar
Miller, A. I. 1988. Spatial resolution in subfossil molluscan remains: implications for paleobiological analyses. Paleobiology 14:91103.Google Scholar
Miller, A. I., Llewellyn, G., Parsons, K. M., Cummins, H., and Boardman, M. R.. 1992. Effect of Hurricane Hugo on molluscan skeletal distributions, Salt River Bay, St. Croix, U.S. Virgin Islands. Geology 20:2326.Google Scholar
Miller, J. H. 2011. Ghosts of Yellowstone: multi-decadal histories of wildlife populations captured by bones on a modern landscape. PLoS ONE 6:e18057.Google Scholar
Nelson, W. G., and Brown, C. A.. 2009. Seagrasses and protective criteria: a review and assessment of research status. Western Ecology Division, National Health and Environmental Effects Research Laboratory, U.S. Environmental Protection Agency, Newport, OR.Google Scholar
Nichols, F. H. 1985. Abundance fluctuations among benthic invertebrates in two Pacific estuaries. Estuaries 8:136144.Google Scholar
Noble, R. S., Curran, H. A., and Wilson, M. A.. 1995. Paleoenvironmental and paleoecologic analyses of a Pleistocene mollusc-rich lagoonal facies, San Salvador Island, Bahamas. Geological Society of America Special Papers 300:91104.Google Scholar
Olszewski, T. D., and Kaufman, D. S.. 2015. Tracing burial history and sediment recycling in a shallow estuarine setting (Copano Bay, Texas) using postmortem ages of the bivalve Mulinia lateralis . Palaios 30:224237.Google Scholar
Parsons-Hubbard, K., Hubbard, D., Tems, C., and Burkett, A.. 2014. The relationship between modern mollusk assemblages and their expression in subsurface sediment in a carbonate lagoon, St. Croix, US Virgin Islands. Pp. 143167 in D. I. Hembree, B. F. Platt, and J. J. Smith, eds. Experimental approaches to understanding fossil organisms: lessons from the living. Springer, New York.Google Scholar
Patriquin, D. G. 1975. Migration of blowouts in seagrass beds at Barbados and Carriacou, West Indies, and its ecological and geological implications. Aquatic Botany 1:163189.Google Scholar
Peterson, C. H. 1982. Clam predation by whelks (Busycon spp.): experimental tests of the importance of prey size, prey density, and seagrass cover. Marine Biology 66:159170.Google Scholar
R Core Team. 2017. R: a language and environment for statistical computing. R Foundation for Statistical Computing, Vienna, Austria.Google Scholar
Redfern, C. 2001. Bahamian seashells: a thousand species from Abaco, Bahamas. Bahamian Seashells, Boca Raton, Fla.Google Scholar
Reise, K. 2002. Sediment mediated species interactions in coastal waters. Journal of Sea Research 48:127141.Google Scholar
Reitz, E. J., and Wing, E. S.. 2008. Zooarchaeology. Cambridge University Press, New York.Google Scholar
Roff, G., Clark, T. R., Reymond, C. E., Zhao, J. X., Feng, Y., McCook, L. J., Done, T. J., and Pandolfi, J. M.. 2013. Palaeoecological evidence of a historical collapse of corals at Pelorus Island, inshore Great Barrier Reef, following European settlement. Proceedings of the Royal Society of London B 280:20122100.Google Scholar
Scarponi, D., Kaufman, D., Amorosi, A., and Kowalewski, M.. 2013. Sequence stratigraphy and the resolution of the fossil record. Geology 41:239242.Google Scholar
Short, F. T., and Wyllie-Echeverria, S.. 1996. Natural and human-induced disturbance of seagrasses. Environmental Conservation 23:1727.Google Scholar
Siebert, T., and Branch, G. M.. 2006. Ecosystem engineers: interactions between eelgrass Zostera capensis and the sandprawn Callianassa kraussi and their indirect effects on the mudprawn Upogebia africana . Journal of Experimental Marine Biology and Ecology 338:253270.Google Scholar
Simões, M., Rodrigues, S., and Kowalewski, M.. 2009. Bouchardia rosea, a vanishing brachiopod species of the Brazilian platform: taphonomy, historical ecology and conservation paleobiology. Historical Biology 21:123137.Google Scholar
Stanley, S. M. 1970. Relation of shell form to life habits of the Bivalvia (Mollusca). Geological Society of America Memoir, Boulder, Colo.Google Scholar
Suchanek, T. H. 1983. Control of seagrass communities and sediment distribution by Callianassa (Crustacea, Thalassinidea) bioturbation. Journal of Marine Research 41:281298.Google Scholar
Terry, R. C. 2010. The dead do not lie: using skeletal remains for rapid assessment of historical small-mammal community baselines. Proceedings of the Royal Society B 324:11931201.Google Scholar
Tomašových, A., and Kidwell, S. M.. 2009. Fidelity of variation in species composition and diversity partitioning by death assemblages: time-averaging transfers diversity from beta to alpha levels. Paleobiology 35:94118.Google Scholar
Tomašových, A., and Kidwell, S. M.. 2010. The effects of temporal resolution on species turnover and on testing metacommunity models. American Naturalist 175:587606.Google Scholar
Tomašových, A., Kidwell, S. M., Barber, R. F., and Kaufman, D. S.. 2014. Long-term accumulation of carbonate shells reflects a 100-fold drop in loss rate. Geology 42:819822.Google Scholar
Widdows, J., Pope, N. D., Brinsley, M. D., Asmus, H., and Asmus, R. M.. 2008. Effects of seagrass beds (Zostera noltii and Z. marina) on near-bed hydrodynamics and sediment resuspension. Marine Ecology Progress Series 358:125136.CrossRefGoogle Scholar
Wilson, M. 1988. Paleoscene #9. Taphonomic processes: information loss and information gain. Geoscience Canada 15:131148.Google Scholar
Yanes, Y. 2012. Anthropogenic effect recorded in the live-dead compositional fidelity of land snail assemblages from San Salvador Island, Bahamas. Biodiversity and Conservation 21:34453466.Google Scholar
Zieman, J. C., and Zieman, R. T.. 1989. The ecology of the seagrass meadows of the west coast of Florida: a community profile: U.S. Fish and Wildlife Service, Washington, D.C. Google Scholar