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

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. "12 Megafauna Biomass Tradeoff as a Driver of Quaternary and Future Extinctions--ANTHONY D. BARNOSKY." 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
FIGURE 12.1 Body-size distribution of mammals in North America. The black bars illustrate the distribution of species that went extinct in the QME. Note that humans are at the lower end of the distribution for species that went extinct. Illustration modified from Lyons et al. (2004); see that source for similar distributions of fauna from other continents.

FIGURE 12.1 Body-size distribution of mammals in North America. The black bars illustrate the distribution of species that went extinct in the QME. Note that humans are at the lower end of the distribution for species that went extinct. Illustration modified from Lyons et al. (2004); see that source for similar distributions of fauna from other continents.

as a whole (Fig. 12.1). Previous work has demonstrated that, as human biomass grows, the amount of solar energy and net primary productivity (NPP) available for use by other species shrinks, ultimately shrinking the amount of the world’s biomass accounted for by those non-human species (Vitousek et al., 1986; Maurer, 1996; Vitousek et al., 1997; McDaniel and Borton, 2002). Therefore, growth of human biomass should be inversely related to biomass of other species in general and to other megafauna species in particular, given that large body size itself to a large extent depends on available NPP. Such energetically driven biomass tradeoffs provide a new way to explore the QME and have the potential of extracting general principles relevant to understanding the future. That is the approach I take here, one that necessarily has many caveats (see Methods), but that nevertheless leads to some interesting observations.

Details of the QME and debates about its causes are summarized in recent reviews (Barnosky et al., 2004; Lyons et al., 2004; Koch and Barnosky, 2006; Wroe and Field, 2006). Salient points include the following. It was a time-transgressive extinction, beginning by 50 kyr B.P. in Australia and largely ending there by 32 kyr B.P., possibly concentrated in an interval between 50 and 40 kyr B.P. (Roberts et al., 2001; Trueman et al., 2005; Wroe and Field, 2006). In northern Eurasia and Beringia, extinctions were later and occurred in two pulses, the first between 48 and 23 kyr B.P. and the second mainly between 14 and 10 kyr B.P. (Koch and Barnosky, 2006), although some species lingered later in isolated regions (Irish elk until 7 kyr B.P. in central Siberia and mammoths until 3 kyr B.P. on Wrangel

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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)