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In the Light of Evolution, Volume II: Biodiversity and Extinction (2008)
National Academy of Sciences (NAS)

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. "3 Patterns of Biodiversity and Endemism on Indo-West Pacific Coral Reefs--MARJORIE L. REAKA, PAULA J. RODGERS, and ALEXEI U. KUDLA." In the Light of Evolution, Volume II: Biodiversity and Extinction. Washington, DC: The National Academies Press, 2008.

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In the Light of Evolution: Volume II—Biodiversity and Extinction

Meyer, 2003; Meyer et al., 2005). In addition to the fact that most benthic reef species are small in body size (Reaka-Kudla, 1997; Bouchet et al., 2002; Meyer et al., 2005) with restricted or moderate colonizing ability, the behavior of reef larvae further reduces dispersal. Stomatopod larvae (and those of most other reef taxa) exhibit diurnal vertical migrations, hiding in reef rubble by day and migrating into the water column at dusk and dawn (Robichaux et al., 1981), which reduces exposure to currents. Although panda clownfish have a 9- to 12-day pelagic phase, one-third of marked juveniles settle within their natal area, many within 100 m of their birth site (GP Jones et al., 2005).

DISCUSSION

Using body size as an indicator of speciation and extinction rates, we infer that the IAA, and to a lesser extent the IOC, are areas of both high origination and high extinction in reef stomatopods. However, rates of origination must exceed those of extinction in these areas, yielding the high biodiversity observed. Endemism results from either newly originated or almost extinct species and thus is expected to be especially high if both speciation and extinction are elevated, as is observed. Although species are concentrated in small size classes in the IAA and IOC, the range of body sizes is large in these areas (see Fig. 3.14). Historical factors (faunal carryover from the Tethys Seaway), productivity in the continental areas, currents, and species diversity itself (via ecological interactions between species) likely have contributed to the species richness and range of body sizes in the IOC and IAA. The dispersal and colonizing capability of large-sized species in these areas allows them to disproportionally colonize adjacent oceanic regions, where extensive larval immigration lowers extinction and retards speciation, yielding moderately diverse, somewhat larger-sized assemblages with low endemism.

In the center of the IO and in the broader expanse of the Pacific, however, larval immigrants have been filtered by starvation, predation, and distance. Given enough time, it is likely that larvae from diversity centers reach mid-ocean islands. However, both diversity and adult body size of reef stomatopods decline in the mid-Pacific, and body size is smaller on mid-Pacific atolls than on high islands, suggesting that productivity of the island environment, as well as propagule pressure, influences successful colonization. Dwarfed by limited productivity, populations cannot produce sufficient propagules to reach another island archipelago and are unlikely to receive many immigrants from ancestral populations to the west. They diverge into new species; endemism increases toward the CP. However, extinction also must be exceedingly high in these small-sized peripheral species. Endemics are missing from atolls, probably reflect-

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Front Matter (R1-R18)
Part I: Contemporary Patterns and Processes in Animals (1-4)
1 Ecological Extinction and Evolution in the Brave New Ocean--JEREMY B. C. JACKSON (5-26)
2 Are We in the Midst of the Sixth Mass Extinction? A View from the World of Amphibians--DAVID B. WAKE and VANCE T. VREDENBURG (27-44)
3 Patterns of Biodiversity and Endemism on Indo-West Pacific Coral Reefs--MARJORIE L. REAKA, PAULA J. RODGERS, and ALEXEI U. KUDLA (45-62)
4 Homage to Linnaeus: How Many Parasites? How Many Hosts?--ANDY DOBSON, KEVIN D. LAFFERTY, ARMAND M. KURIS, RYAN F. HECHINGER, and WALTER JETZ (63-82)
Part II: Contemporary Patterns and Processes in Plants and Microbes (83-84)
5 Species Invasions and Extinction: The Future of Native Biodiversity on Islands--DOV F. SAX and STEVEN D. GAINES (85-106)
6 How Many Tree Species Are There in the Amazon and How Many of Them Will Go Extinct?--STEPHEN P. HUBBELL, FANGLIANG HE, RICHARD CONDIT, LUIS BORDA-DE-ÁGUA, JAMES KELLNER, and HANS TER STEEGE (107-126)
7 Microbes on Mountainsides: Contrasting Elevational Patterns of Bacterial and Plant Diversity--JESSICA A. BRYANT, CHRISTINE LAMANNA, HÉLÈNE MORLON, ANDREW J. KERKHOFF, BRIAN J. ENQUIST, and JESSICA L. GREEN (127-148)
8 Resistance, Resilience, and Redundancy in Microbial Communities--STEVEN D. ALLISON and JENNIFER B. H. MARTINY (149-166)
Part III: Trends and Processes in the Paleontological Past (167-170)
9 Extinction as the Loss of Evolutionary History--DOUGLAS H. ERWIN (171-188)
10 Extinction and the Spatial Dynamics of Biodiversity--DAVID JABLONSKI (189-206)
11 Dynamics of Origination and Extinction in the Marine Fossil Record--JOHN ALROY (207-226)
12 Megafauna Biomass Tradeoff as a Driver of Quaternary and Future Extinctions--ANTHONY D. BARNOSKY (227-242)
Part IV: Prospects for the Future (243-246)
13 A Phylogenetic Perspective on the Distribution of Plant Diversity--MICHAEL J. DONOGHUE (247-262)
14 Phylogenetic Trees and the Future of Mammalian Biodiversity--T. JONATHAN DAVIES, SUSANNE A. FRITZ, RICHARD GRENYER, C. DAVID L. ORME, JON BIELBY, OLAF R. P. BININDA-EMONDS, MARCEL CARDILLO, KATE E. JONES, JOHN L. GITTLEMAN, GEORGINA M. MACE, and ANDY PURVIS (263-280)
15 Three Ambitious (and Rather Unorthodox) Assignments for the Field of Biodiversity Genetics--JOHN C. AVISE (281-296)
16 Engaging the Public in Biodiversity Issues--MICHAEL J. NOVACEK (297-316)
17 Further Engaging the Public on Biodiversity Issues--PETER J. BRYANT (317-328)
18 Where Does Biodiversity Go from Here? A Grim Business-as-Usual Forecast and a Hopeful Portfolio of Partial Solutions--PAUL R. EHRLICH and ROBERT M. PRINGLE (329-346)
References (347-394)
Index (395-414)