Hostname: page-component-78c5997874-4rdpn Total loading time: 0 Render date: 2024-11-18T07:18:37.613Z Has data issue: false hasContentIssue false

Coral reef development drives molluscan diversity increase at local and regional scales in the late Neogene and Quaternary of the southwestern Caribbean

Published online by Cambridge University Press:  08 April 2016

Kenneth G. Johnson
Affiliation:
Department of Palaeontology, The Natural History Museum, Cromwell Road, London SW7 5BD, United Kingdom. E-mail: [email protected]
Jonathan A. Todd
Affiliation:
Department of Palaeontology, The Natural History Museum, Cromwell Road, London, SW7 5BD, United Kingdom. E-mail: [email protected]
Jeremy B. C. Jackson
Affiliation:
Geosciences Research Division, Scripps Institution of Oceanography, University of California, San Diego, La Jolla, California 92093-0244, and Smithsonian Tropical Research Institute, Box 2072, Balboa, Republic of Panama. E-mail: [email protected]

Abstract

The late Neogene was a time of major environmental change in Tropical America. Global cooling and associated oceanographic reorganization and the onset and intensification of glaciation in the Northern Hemisphere during the past ten million years coincided with the uplift of the Central American isthmus and resulting changes in regional oceanographic conditions. Previous analyses of patterns of taxonomic turnover and the shifting abundances of major ecological guilds indicated that the regional shallow-water marine biota responded to these environmental changes through extinction and via a restructuring of local benthic food webs, but it is not clear whether this ecological response had an effect on the diversity of molluscan assemblages in the region. Changes in regional and local diversity are often used as proxies for similar ecological response to environmental change in large-scale paleontological studies, but a clear relationship between diversity and ecological function has rarely been demonstrated in marine systems dominated by mollusks. To explore this relationship, we have compiled a data set of the stratigraphic and environmental distribution of genera of mollusks in large new collections of fossil specimens from the late Neogene and Recent of the southwestern Caribbean. Analysis of a selection of ecological diversity measures indicates that within shelf depths, assemblages from deeper water (51–200 m) were more diverse than shallow-water (<50 m) assemblages in the Pliocene. Lower diversity for shallow-water assemblages is caused by increased dominance of a few superabundant taxa in each assemblage. This implies that studies of diversity of shelf benthos need to control for relatively fine scaled environmental conditions if they are to avoid interpreting artifacts of uneven sampling as true change of diversity. For shallow-water assemblages only, there was significant increase in local and regional diversity of bivalve assemblages after the late Pliocene. No parallel increase in gastropods could be detected, but this likely is because sample size was inadequate for documenting the diversity of gastropod assemblages following a steep post-Pliocene decline of average gastropod abundance. Both the increasing bivalve diversity and the decrease in average abundance of gastropod taxa correspond to an interval of increasing carbonate deposition and reef building in the region, and are likely a result of increased fine-scale habitat heterogeneity controlled by the local distribution of carbonate buildups. Each of these results demonstrates that documenting the ecological response of tropical marine ecosystems to regional environmental change requires a large volume of fine-scaled samples with detailed paleoenvironmental control. Such data sets are rarely available from the fossil record.

Type
Articles
Copyright
Copyright © The Paleontological Society 

Access options

Get access to the full version of this content by using one of the access options below. (Log in options will check for institutional or personal access. Content may require purchase if you do not have access.)

References

Literature Cited

Allmon, W. D. 1988. Ecology of Recent turritelline gastropods (Prosobranchia, Turritellidae): current knowledge and paleontological implications. Palaios 3:259284.Google Scholar
Allmon, W. D. 2001. Nutrients, temperature, disturbance, and evolution: a model for the late Cenozoic marine record of the western Atlantic. Palaeogeography, Palaeoclimatology, Palaeoecology 166:926.CrossRefGoogle Scholar
Allmon, W. D., Rosenberg, G., Portell, R. W., and Schindler, K. 1993. Diversity of Pliocene to Recent Atlantic coastal plain mollusks. Science 260:16261628.CrossRefGoogle ScholarPubMed
Allmon, W. D., Emslie, S. D., Jones, D. S., and Morgan, G. S. 1996. Late Neogene oceanographic change along Florida's west coast: evidence and mechanisms. Journal of Geology 104:143162.Google Scholar
Alroy, J., Marshall, C. R., Bambach, R. K., Bezusko, K., Foote, M., Fursich, F. T., Hansen, T. A., Holland, S. M., Ivany, L. C., Jablonski, D., Jacobs, D. K., Jones, D. C., Kosnick, M. A., Lidgard, S., Low, S., Miller, A. I., Novack-Gottshall, P. M., Olszewski, T. D., Patzkowsky, M. E., Raup, D. M., Roy, K., Sepkoski, J. J. Jr., Sommers, M. G., Wagner, P. J., and Webber, A. 2001. Effects of sampling standardization on estimates of Phanerozoic marine diversification. Proceedings of the National Academy of Sciences USA 98:62616266.Google Scholar
Andréfouet, S., and Guzman, H. M. 2005. Coral reef distribution, status and geomorphology-biodiversity relationship in Kuna Yala (San Blas) archipelago, Caribbean Panama. Coral Reefs 24:3142.CrossRefGoogle Scholar
Aubry, M.-P., and Berggren, W. A. 1999. Newest biostratigraphy. Pp. 3841 in Collins, and Coates, 1999a.Google Scholar
Bengtson, P. 1988. Open nomenclature. Palaeontology 31:223227.Google Scholar
Berggren, W. A., Kent, D. V., Swisher, C. C. III, and Aubry, M.-P. 1995. A revised Cenozoic geochronology and chronostratigraphy. In Berggren, W. A., Kent, D. V., Aubry, M.-P., and Hardenbol, J., eds. Geochronology, time scales, and global stratigraphic correlation. Society for Sedimentary Geology Special Publication 54:129212.Google Scholar
Berger, W. H., and Wefer, G. 1996. Expeditions into the past: paleoceanographic studies in the South Atlantic. Pp. 363410 in Wefer, G., Berger, W. H., Siedler, G., and Webb, D. J., eds. The South Atlantic: Present and past circulation. Springer, Berlin.CrossRefGoogle Scholar
Best, M. M. R., and Kidwell, S. M. 2000. Bivalve taphonomy in tropical mixed siliciclastic-carbonate settings. I. Environmental variation in shell condition. Paleobiology 26:80102.Google Scholar
Birkeland, C. 1987. Nutrient availability as a major determinant of differences among coastal hard-substratum communities in different regions of the tropics. UNESCO Reports in Marine Science 46:4597.Google Scholar
Bitter-Soto, R. 1999. Benthic communities associated to Thalassia testudinum (Hydrocharitaceae) at three localities of Marrocoy National Park, Venezuela. Revista de Biología Tropical 47:443452.Google Scholar
Borne, P. F., Cronin, T. M., and Hazel, J. E. 1999. Neogene-Quaternary Ostracoda and paleoenvironments of the Limon Basin, Costa Rica and Bocas del Toro Basin, Panama. Pp. 231250 in Collins, and Coates, 1999a.Google Scholar
Bouchet, P., Lozouet, P., Maestrati, P., and Heros, V. 2002. Assessing the magnitude of species richness in tropical marine environments: exceptionally high numbers of molluscs at a New Caledonia site. Biological Journal of the Linnean Society 75:421436.Google Scholar
Budd, A. F., and Foster, C. T. Jr., coordinators. 1996–2006. Neogene marine biota of tropical America (NMITA): a worldwide web taxonomy database. Available online at http://nmita.geology.uiowa.edu.Google Scholar
Budd, A. F., and Johnson, K. G. 2001. Contrasting patterns in rare and abundant species during evolutionary turnover. Pp. 295325 in Jackson, J. B. C., Lidgard, S., and McKinney, F. K., eds. Process from pattern in the fossil record. University of Chicago Press, Chicago.Google Scholar
Budd, A. F., Stemann, T. A., and Johnson, K. G. 1994. Stratigraphic distributions of genera and species of Neogene to Recent reef corals. Journal of Paleontology 68:951977.Google Scholar
Budd, A. F., Johnson, K. G., and Stemann, T. A. 1996. Plio-Pleistocene turnover and extinctions in the Caribbean coral-reef fauna. Pp. 168204 in Jackson, et al. 1996.Google Scholar
Budd, Ann F., Johnson, K. G., Stemann, T. A., and Tompkins, B. H. 1999. Pliocene to Pleistocene reef coral assemblages in the Limon Group of Costa Rica. Pp. 119158 in Collins, and Coates, 1999a.Google Scholar
Buzas, M. A., and Hayek, L.-A. C. 2005. On richness and evenness within and between communities. Paleobiology 32:199220.Google Scholar
Bybell, L. M. 1999. Neogene calcareous nannofossil biostratigraphy of the Caribbean coast of Panama and Costa Rica. Pp. 4160 in Collins, and Coates, 1999a.Google Scholar
Cabin, R. J., and Mitchell, R. J. 2000. To Bonferroni or not to Bonferroni: when and how are the questions. Bulletin of the Ecological Society of America 81:246248.Google Scholar
Cheetham, A. H., and Jackson, J. B. C. 1996. Speciation, extinction, and the decline of arborescent growth in Neogene and Quaternary cheilostome Bryozoa of tropical America. Pp. 205233 in Jackson, et al. 1996.Google Scholar
Cheetham, A. H., Jackson, J. B. C., Sanner, J., and Ventocilla, Y. 1999. Neogene cheilostome Bryozoa of tropical America: Comparison and contrast between Central American Isthmus (Panama, Costa Rica) and the north-central Caribbean (Dominican Republic). Pp. 159192 in Collins, and Coates, 1999a.Google Scholar
Coates, A. G. 1999a. Lithostratigraphy of the Neogene strata of the Caribbean coast from Limon, Costa Rica, to Colon, Panama. Pp. 1737 in Collins, and Coates, 1999a.Google Scholar
Coates, A. G. 1999b. Appendix B: stratigraphic sections. Pp. 299348 in Collins, and Coates, 1999a.Google Scholar
Coates, A. G., Jackson, J. B. C., Collins, L. S., Cronin, T. S., Dowsett, H. J., Bybell, L. M., Jung, P., and Obando, J. A. 1992. Closure of the Isthmus of Panama: the near-shore marine record of Costa Rica and Panama. Geological Society of America Bulletin 104:814828.2.3.CO;2>CrossRefGoogle Scholar
Coates, A. G., Aubry, M.-P., Berggren, W. A., Collins, L. S., and Kunk, M. 2003. Early Neogene history of the Central American arc from Bocas del Toro, western Panama. Geological Society of America Bulletin 115:271287.2.0.CO;2>CrossRefGoogle Scholar
Coates, A. G., Collins, L. S., Aubry, M.-P., and Berggren, W. A. 2004a. The geology of the Darien, Panama, and the late Miocene-Pliocene collision of the Panama arc with northwestern South America. Geological Society of America Bulletin 116:13271344.Google Scholar
Coates, A. G., Collins, L. S., Aubry, M.-P., and Berggren, W. A. 2004b. Data repository item 2004169. Available online at http://www.geosociety.org/pubs/ft2004.htm Google Scholar
Collins, L. S. 1993. Neogene paleoenvironments of the Bocas del Toro Basin, Panama. Journal of Paleontology 67:699710.CrossRefGoogle Scholar
Collins, L. S. 1999. The Miocene to Recent diversity of Caribbean benthic foraminifera from the Central American isthmus. Pp. 91108 in Collins, and Coates, 1999a.Google Scholar
Collins, L. S., and Coates, A. G., eds. 1999a. A paleobiotic survey of the Caribbean faunas from the Neogene of the Isthmus of Panama. Bulletins of American Paleontology 357.Google Scholar
Collins, L. S., and Coates, A. G. 1999b. Introduction. Pp. 513 in Collins, and Coates, 1999a.Google Scholar
Collins, L. S., Budd, A. F., and Coates, A. G. 1996a. Earliest evolution associated with closure of the Tropical American Seaway. Proceedings of the National Academy of Sciences USA 93:60696072.CrossRefGoogle ScholarPubMed
Collins, L. S., Coates, A. G., Berggren, W. A., Aubry, M.-P., and Zhang, J. 1996b. The Late Miocene Panama isthmian strait. Geology 24:687690.2.3.CO;2>CrossRefGoogle Scholar
Collins, L. S., Aguilera, O., Borne, P. F., and Cairns, S. D. 1999. A paleoenvironmental analysis of the Neogene of Caribbean Panama and Costa Rica using several phyla. Pp. 8190 in Collins, and Coates, 1999a.Google Scholar
Cotton, M. A. 1999. Neogene planktic foraminiferal biochronology of the southern Central American isthmus. Pp. 6180 in Collins, and Coates, 1999a.Google Scholar
Crampton, J. S., Foote, M., Beu, A. G., Coope, R. A., Matcham, I., Jones, C. M., Maxwell, P. A., and Marshall, B. A. 2006. Second-order sequence stratigraphic controls on the quality of the fossil record at an active margin: New Zealand Eocene to Recent shelf molluscs. Palaios 21:86105.Google Scholar
Domning, D. P. 2001. Sirenians, seagrasses, and Cenozoic ecological change in the Caribbean. Palaeogeography, Palaeoclimatology, Palaeoecology 166:2750.CrossRefGoogle Scholar
Done, T. J., Ogden, J. C., Wiebe, W. J., and Rosen, B. R. 1996. Biodiversity and ecosystem function of coral reefs. Pp. 393429 in Mooney, H. A., Cushman, J. H., Medina, E., Sala, O. E., and Schulze, E.-D., eds. Functional roles of biodiversity: a global perspective. Wiley, Chichester, U.K. Google Scholar
Ellingsen, K. E. 2001. Biodiversity of a continental shelf soft-sediment macrobenthos community. Marine Ecology Progress Series 218:115.Google Scholar
Ellingsen, K. E. 2002. Soft-sediment benthic biodiversity on the continental shelf in relation to environmental variability. Marine Ecology Progress Series 232:1527.Google Scholar
Fedorov, A. V., Dekens, P. S., McCarthy, M., Ravelo, A. C., deMenocal, P. B., Barreiro, M., Pacanowski, R. C., and Philander, S. G. 2006. The Pliocene paradox (mechanisms for a permanent El Niño). Science 312:14851489.Google Scholar
Gardiner, L. 2001. Stability of late Pleistocene reef mollusks from San Salvador Island, Bahamas. Palaios 16:372386.Google Scholar
Getty, S. R., Asmerom, Y., Quinn, T. M., and Budd, A. F. 2001. Accelerated Pleistocene coral extinctions in the Caribbean Basin shown by uranium-lead (U-Pb) dating. Geology 29:639642.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
Gray, J. S. 1997. Gradients in marine biodiversity Pp. 1834 in Ormond, R. F. G., Gage, J. D., and Angel, M. V., eds. Marine biodiversity: patterns and processes. Cambridge University Press, Cambridge.Google Scholar
Gray, J. S., Poore, G. C. B., Ugland, K. I., Wilson, R. S., Olsgard, F., and Johannessen, Ø. 1997. Coastal and deep sea benthic diversities compared. Marine Ecology Progress Series 159:97103.Google Scholar
Hallock, P., and Schlager, W. 1986. Nutrient excess and the demise of coral reefs and carbonate platforms. Palaios 1:389398.Google Scholar
Haug, G. H., and Tiedemann, R. 1998. Effect of the formation of the Isthmus of Panama on Atlantic Ocean thermohaline circulation. Nature 393:673676.CrossRefGoogle Scholar
Hayek, L.-A. C., and Buzas, M. A. 1997. Surveying natural populations. Columbia University Press, New York.Google Scholar
Heck, K. L. Jr. 1977. Comparative species richness, composition, and abundance of invertebrates in Caribbean seagrass (Thalassia testudinum) meadows (Panamá). Marine Biology 41:335358.Google Scholar
Hessler, R. R., and Sanders, H. L. 1967. Faunal diversity in the deep sea. Deep-Sea Research 14:6578.Google Scholar
Hill, K. 2002. Seagrass habitats. Available online at http://www.sms.si.edu/irlspec/Seagrass_Habitat.htm (Smithsonian Marine Station at Fort Pierce website).Google Scholar
Holland, S. M. 2000. The quality of the fossil record: a sequence stratigraphic perspective. In Erwin, D. H. and Wing, S. L., eds. Deep time: Paleobiology‘s perspective. Paleobiology 26(Suppl. to No. 4):148168.Google Scholar
Hughes, T. P. 1994. Catastrophes, phase shifts, and large-scale degradation of a Caribbean coral reef. Science 265:15471551.Google Scholar
Jablonski, D., Lidgard, S., and Taylor, P. D. 1997. Comparative ecology of bryozoan radiations: origin of novelties in cyclostomes and cheilostomes. Palaios 12:505523.Google Scholar
Jackson, J. B. C. 1973. The ecology of mollusks of Thalassia communities, Jamaica, West Indies. I. Distribution, environmental physiology, and ecology of common shallow-water species. Bulletin of Marine Science 23:313350.Google Scholar
Jackson, J. B. C. 1994a. Community unity? Science 264:14121413.Google Scholar
Jackson, J. B. C. 1994b. Constancy and change of life in the sea. Philosophical Transactions of the Royal Society of London B 344:5560.Google Scholar
Jackson, J. B. C., and Budd, A. F. 1996. Evolution and environment: introduction and overview. Pp. 120 in Jackson, et al. 1996.Google Scholar
Jackson, J. B. C., and D'Croz, L. 1997. The ocean divided. Pp. 3871 in Coates, A. G., ed. Central America: a natural and cultural history. Yale University Press, New Haven, Conn. Google Scholar
Jackson, J. B. C., and Johnson, K. G. 2000. Life in the last few million years. In Erwin, D. H. and Wing, S. L., eds. Deep time: Paleobiology‘s perspective. Paleobiology 26(Suppl. to No. 4):221235.Google Scholar
Jackson, J. B. C., Jung, P., Coates, A. G., and Collins, L. S. 1993. Diversity and extinction of tropical American mollusks and the emergence of the Isthmus of Panama. Science 260:16241626.Google Scholar
Jackson, J. B. C., Budd, A. F., and Coates, A. G., eds. 1996. Evolution and environment in tropical America. University of Chicago Press, Chicago.Google Scholar
Jackson, J. B. C., Todd, J. A., Fortunato, H., and Jung, P. 1999. Diversity and assemblages of Neogene Caribbean Mollusca of lower Central America. Pp. 193230 in Collins, and Coates, 1999a.Google Scholar
Johnson, K. G., and Kirby, M. X. 2006. The Emperador Limestone rediscovered: Early Miocene corals from the Culebra Formation, Panama. Journal of Paleontology 80:283293.Google Scholar
Johnson, K. G., and Pérez, M. E. 2006. Skeletal extension rates of Cenozoic Caribbean reef corals. Palaios 21:262271.Google Scholar
Johnson, K. G., Budd, A. F., and Stemann, T. A. 1995. Extinction selectivity and ecology of Neogene Caribbean corals. Paleobiology 21:5273.Google Scholar
Jones, D. S., and Hasson, P. F. 1985. History and development of the marine invertebrate faunas separated by the Central American Isthmus. Pp. 325355 in Stehli, F. G. and Webb, S. D., eds. The Great American biotic interchange. Plenum, New York.Google Scholar
Keigwin, L. D. 1978. Pliocene closing of the Isthmus of Panama based on biostratigraphic evidence from nearby Pacific Ocean and Caribbean Sea cores. Geology 6:63634.Google Scholar
Kidwell, S. M., Best, M. M. R., and Kaufman, D. S. 2005. Taphonomic trade-offs in tropical marine death assemblages: differential time averaging, shell loss, and probable bias in siliciclastic vs. carbonate facies. Geology 33:729732.Google Scholar
Knowlton, N. 1992. Thresholds and multiple stable states in coral reef community dynamics. American Zoologist 32:674682.Google Scholar
Kohn, A. J. 2001. Maximal species richness in Conus: diversity, diet and habitat on reefs of northeast Papua New Guinea. Coral Reefs 20:2538.Google Scholar
Lee, T., and Foighil, D. Ó. 2004. Hidden Floridian biodiversity: mitochondrial and nuclear gene trees reveal four cryptic species within the scorched mussel, Brachidontes exustus, species complex. Molecular Ecology 13:35273542.Google Scholar
Magurran, A. E. 2004. Measuring biological diversity. Blackwell Science, Oxford.Google Scholar
McCoy, E. D., and Heck, K. L. 1976. Biogeography of corals, seagrasses, and mangroves: an alternative to the center of origin concept. Systematic Zoology 25:201210.Google Scholar
McNeill, D. F., Coates, A. G., Budd, A. F., and Borne, P. F. 2000. Integrated biological and paleomagnetic stratigraphy of the Late Neogene deposits around Limon Costa Rica: a coastal emergence record of the Central American Isthmus. Geological Society of American Bulletin 112:963981.Google Scholar
Meldahl, K. H., Flessa, K. W., and Cutler, A. H. 1997. Time-averaging and postmortem skeletal survival in benthic fossil assemblages: quantitative comparisons among Holocene environments. Paleobiology 23:207229.Google Scholar
Meyer, C. P., Geller, J. B., and Paulay, G. 2005. Fine scale endemism on coral reefs: archipelagic differentiation in turbinid gastropods. Evolution 59:113125.Google Scholar
Mikkelsen, P. M., and Bieler, R. 2000. Marine bivalves of the Florida Keys: discovered biodiversity. In Harper, E. M., Taylor, J. D., and Crame, J. A., eds. The evolutionary biology of the Bivalvia. Geological Society of London Special Publication 177:367387.Google Scholar
Mittelbach, G. G., Steiner, C. F., Scheiner, S. M., Gross, K. L., Reynolds, H. L., Waide, R. B., Willig, M. R., Dodson, S. I., and Gough, L. 2001. What is the observed relationship between species richness and productivity? Ecology 82:23812396.CrossRefGoogle Scholar
Morrison, C. L., Ríos, R., and Duffy, J. E. 2004. Phylogenetic evidence for an ancient rapid radiation of Caribbean spongedwelling snapping shrimps (Synalpheus). Molecular Phylogenetics and Evolution 30:563581.Google Scholar
Ogden, J. 1997. Ecosystem interactions in the tropical coastal seascape. Pp. 288297 in Birkeland, C., ed. Life and death of coral reefs. Chapman and Hall, New York.Google Scholar
Ogden, J. C., and Ogden, N. B. 1998. Reconnaissance survey of the coral reefs and associated ecosystems of Cayos Cochinos, Honduras. Revista de Biología Tropical 46(Suppl. 4):6774.Google Scholar
Parsons-Hubbard, K. 2005. Molluscan taphofacies in Recent carbonate reef/lagoon systems and their application to sub-fossil samples from reef cores. Palaios 20:175191.Google Scholar
Paulay, G. 1997. Diversity and distribution of reef organisms. Pp. 298353 in Birkeland, C., ed. Life and death of coral reefs. Chapman and Hall, New York.Google Scholar
Peterson, C. H. 1979. Predation, competitive exclusion, and diversity in the soft-sediment benthic communities of estuaries and lagoons. Pp. 223264 in Livingstone, R. J., ed. Ecological processes in coastal and marine systems. Plenum, New York.Google Scholar
Petuch, E. J. 1982. Geographical heterochrony: contemporaneous coexistence of Neogene and Recent molluscan faunas in the Americas. Palaeogeography, Palaeoclimatology, Palaeoecology 37:277312.Google Scholar
R Development Core Team. 2005. R: a language and environment for statistical computing. R Foundation for Statistical Computing, Vienna. Available online at http://www.R-project.org. [Checked 23 November 2005.] Google Scholar
Raup, D. M. 1972. Taxonomic diversity during the Phanerozoic. Science 177:10651071.Google Scholar
Raymo, M. E. 1994. The initiation of Northern Hemisphere glaciation. Annual Review of Earth and Planetary Sciences 22:353383.Google Scholar
Reaka-Kudla, M. L. 1997. The global biodiversity of coral reefs: a comparison with rain forests. Pp. 83108 in Reaka-Kudla, M. L., Wilson, D. E., and Wilson, E. O., eds. Biodiversity II: understanding and protecting our biological resources. Joseph Henry Press, Washington, D.C. Google Scholar
Rex, M. A. 1981. Community structure in the deep-sea benthos. Annual Review of Ecology and Systematics 12:332353.Google Scholar
Rex, M. A., Etter, R. J., and Stuart, C.T. 1997. Large scale patterns of biodiversity in the deep-sea benthos. Pp. 94121 in Ormond, R. F. G., Gage, J. D., and Angel, M. V., eds. Marine biodiversity: patterns and processes. Cambridge University Press, Cambridge.Google Scholar
Rice, W. R. 1989. Analyzing tables of statistical tests. Evolution 43:223225.Google Scholar
Rüber, L., Van Tassel, J. L., and Zadoya, R. 2003. Rapid speciation and ecological divergence in the American Seven-spined Gobies (Gobiidae, Gobiosomatini) inferred from a molecular phylogeny. Evolution 57:15841598.Google Scholar
Schlacher, T. A., Newell, P., Clavier, J., Schlacher-Hoenlinger, M. A., Chevillon, C., and Britton, J. 1998. Soft-sediment benthic community structure in a coral reef lagoon—the prominence of heterogeneity and ‘spot endemism.’ Marine Ecology Progress Series 174:159174.Google Scholar
Schluter, D., and Ricklefs, R. E. 1993. Species diversity: an introduction to the problem. Pp. 110 in Ricklefs, R. E. and Schluter, D., eds. Species diversity in ecological communities: historical and geographical perspectives. University of Chicago Press, Chicago.Google Scholar
Shin, P. K. S., and Ellingsen, K. E. 2004. Spatial patterns of soft-sediment benthic diversity in subtropical Hong Kong waters. Marine Ecology Progress Series 276:2535.Google Scholar
Spalding, M. D., Ravilious, C., and Green, E. P. 2001. World atlas of coral reefs. University of California Press, Berkeley.Google Scholar
Stanley, S. M. 1986. Anatomy of a regional mass extinction: Plio-Pleistocene decimation of the western Atlantic bivalve fauna. Palaios 1:1736.Google Scholar
Stanley, S. M., and Campbell, L. D. 1981. Neogene mass extinction of Western Atlantic molluscs. Nature 293:457459.Google Scholar
Taylor, M. S., and Hellberg, M. E. 2005. Marine radiations at small geographic scales: speciation in Neotropical reef gobies (Elacatinus). Evolution 59:374385 Google Scholar
Terranes, J. L., Geary, D. H., and Bemis, B. E. 1996. The oxygen isotopic record of seasonality in Neogene bivalves from the Central American Isthmus. Pp. 105129 in Jackson, et al. 1996.Google Scholar
Tilman, D., Lehman, C. L., and Bristow, C. E. 1998. Diversity-stability relationships: statistical inevitability or ecological consequence? American Naturalist 151:277282.Google Scholar
Tipper, J. C. 1979. Rarefaction and rarefiction: the use and abuse of a method in paleoecology. Paleobiology 5:423434.CrossRefGoogle Scholar
Todd, J. A. 2001a. Identification and taxonomic consistency. In Budd, and Foster, 1996–2006. Available online at http://nmita.geology.uiowa.edu/database/mollusc/molluscintro.htm Google Scholar
Todd, J. A. 2001b. Introduction to molluscan life habits databases. In Budd, and Foster, 1996–2006. Available online at http://nmita.geology.uiowa.edu/database/mollusc/mollusclifestyles.htm. [Last checked 10 October 2006.] Google Scholar
Todd, J. A. 2005a. Systematic list of bivalves in the Panama Paleontology Project collections. In Budd, and Foster, 1996–2006.Google Scholar
Todd, J. A. 2005b. Systematic list of gastropods in the Panama Paleontology Project collections. In Budd, and Foster, 1996–2006.Google Scholar
Todd, J. A., and Collins, J. S. H. 2006. Neogene and Quaternary crabs (Crustacea, Decapoda) collected from Costa Rica and Panama by members of the Panama Paleontology Project. Bulletin of the Mizunami Fossil Museum 32:5385 + 4 plates.Google Scholar
Todd, J. A., and Rawlings, T. A. 2003. Exploring the evolutionary radiation of the marine gastropod genus Polystira within Tropical America, Part I. Introduction and shell morphological diversity. P. 59 in Foighil, D. Ó and Lee, T., eds. Program and abstracts. American Malacological Society 69th Annual Meeting, Ann Arbor, Mich. Google Scholar
Todd, J. A., Jackson, J. B. C., Johnson, K. G., Fortunato, H. M., Heitz, A., and Jung, P. 2002. The ecology of extinction: molluscan feeding and faunal turnover in the Caribbean Neogene. Proceedings of the Royal Society of London B 269:571577.Google Scholar
Vaughan, T. W. 1919. Fossil corals from Central America, Cuba, and Porto Rico, with an account of the American Tertiary, Pleistocene, and Recent coral reefs. U.S. National Museum Bulletin 103:189524.Google Scholar
Vermeij, G. 1989. Interoceanic differences in adaptation: effects of history and productivity. Marine Ecology Progress Series 57:293305.Google Scholar
Vermeij, G. J. 2001. Community assembly in the sea: geologic history of the living shore biota. Pp. 3960 in Bertness, M. D., Gaines, S. D., and Hay, M. E., eds. Marine community ecology. Sinauer, Sunderland, Mass. Google Scholar
Vermeij, G. J., and Petuch, E. J. 1986. Differential extinction in tropical American mollusks: endemism, architecture, and the Panama land bridge. Malacologia 27:2941.Google Scholar
Waide, R. B., Willig, M. R., Steiner, C. F., Mittelbach, G., Gough, L., Dodson, S. I., Juday, G. P., and Parmenter, R. 1999. The relationship between productivity and species richness. Annual Review of Ecology and Systematics 30:257300.Google Scholar
Woodring, W. P. 1966. The Panama land bridge as a sea barrier. Proceedings of the American Philosophical Society 110:425433.Google Scholar
Zachos, J., Pagani, M., Sloan, L., Thomas, E., and Billups, K. 2001. Trends, rhythms, and aberrations in global climate 65 Ma to present. Science 292:686693.Google Scholar
Supplementary material: File

Johnson et al. supplementary material

Appendix

Download Johnson et al. supplementary material(File)
File 280.1 KB