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

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. "4 Homage to Linnaeus: How Many Parasites? How Many Hosts?--ANDY DOBSON, KEVIN D. LAFFERTY, ARMAND M. KURIS, RYAN F. HECHINGER, and WALTER JETZ." 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

However, studies from Beringia (in the high Arctic) suggest that significant levels of parasite interchange occur during intermittent periods of climatic warming when host species from the arctic regions of different continents disperse across the poles and provide new host opportunities for their parasites (Hoberg and Adams, 1992).

If the range size of avian species, orders, and families increases with distance from the equator (Fig. 4.4), might we see a similar effect with the range size of parasites? If so, then this will have caused us to further underestimate the diversity of parasites in the tropics, because the area sampled by tropical parasite taxonomists is tiny. Similarly, do the nested patterns of geographical diversity for the hosts reflect pulses of radiation and speciation between the tropics and temperate zones after past periods of climate change, and would we see similar radiations of diversity if we traced the phylogenies and geographical distributions of avian parasites at different taxonomic levels? Surveys suggest that the diversity of human parasites is significantly higher in the tropics (Low, 1990; Guernier et al., 2004), but as we saw above, this is less clearly the case for fish parasites. If similar latitudinal patterns occur in avian orders and genera, and if parasites are responsible for driving significant components of sexual selection that lead to host speciation, then we might expect complex patterns of geographical variation in parasite diversity at the taxonomic level of host order and family. Unfortunately, the parasite data with which to test these hypotheses are unavailable.

LOSS OF AVIAN DIVERSITY: CLIMATE CHANGE VERSUS HABITAT LOSS

We have used the geographic distribution database for birds described above to evaluate potential impacts of projected environmental change on each of the major continents (Jetz et al., 2007). The Millennium Ecosystem Assessment (MEA) used four quantitative scenarios to examine how land cover would change across the land surface of the Earth over the next 50 and 100 years (Alcamo et al., 2005; Carpenter et al., 2005). The scenarios were driven by quantitative climate models derived from the Intergovernmental Panel on Climate Change (IPCC) and projections of human population growth, wealth, and other socioeconomic parameters across regions (Image_Team, 2001). In these projections, rates of land conversion would be driven either by climate change or by the need for new agriculture land. The four MEA scenarios were defined by whether or not governments take a proactive or reactive response to environmental management, and by whether the world’s nations become more unified and interactive or they become more protectionist and isolated (Cork et al., 2005). Jetz et al. (2007) used the output from the scenarios to examine the

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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)