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

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. "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." 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

community and the expected distribution of relative species abundance and species range sizes. The “metacommunity” refers to the evolutionary–biogeographic unit in which most member species spend their entire evolutionary lifetimes, from origination to extinction, a concept apropos to the entire Amazon Basin. Neutral theory generates a biodiversity number θ that uniquely specifies not only how many species are expected to be present at steady state between speciation and extinction in the metacommunity but also the expected abundances of each species. The number θ is a fundamental quantity in neutral theory that is proportional to the product of the average per capita speciation rate in the metacommunity and the size of the metacommunity. Metacommunity size is simply the sum of the population sizes of all species in the metacommunity. An important discovery from neutral theory is that the expected distribution of metacommunity relative species abundance is Fisher’s logseries (Hubbell, 2001; Volkov et al., 2003).

The logseries distribution applies in cases when the metacommunity is continuous, as in continental tropical forests, but not necessarily if an island model is more appropriate for the metacommunity, as in the case of isolated coral reefs scattered across the Pacific Ocean (Volkov et al., 2007). Remarkably, it also turns out that the fundamental biodiversity number θ of neutral theory is identical to Fisher’s α, the celebrated diversity index of Fisher’s logseries, and parameter x of the logseries is the ratio of the average per capita birth rate to per capita death rate in the metacommunity. The reason Fisher’s α is so stable, according to neutral theory, is that it is proportional to the average speciation rate in the metacommunity and to the size of the metacommunity, both very stable numbers.

How do we fit Fisher’s logseries when the total number of tree species in the Amazon and their relative abundances are unknown? Extensive areas of the Amazon have not yet been adequately collected. Moreover, a large amount of material already collected remains to be described and classified for the first time, and many groups need revision to eliminate synonyms for species described multiple times from collections made by different museums at different times from different parts of Amazonia. Despite current problems with species-level identifications, however, generic-level determinations of Amazonian trees are much more reliable. Most undescribed tree species can at least be placed with reasonable confidence into a known genus. This is fortunate because we can test the fit of the logseries and the lognormal to the abundances of Amazonian genera.

Neutral theory asserts that generic- and familial-level clades should also obey the same metacommunity dynamics as species, the only difference being that they should have lower rates of origination and extinction than species do. Over the last two decades, a dataset comprising over

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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)