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Nature 427, 107 - 109 (08 January 2004); doi:10.1038/427107a Ecology: Clouded futures J. ALAN POUNDS AND ROBERT PUSCHENDORF J. Alan Pounds is at the Golden Toad Laboratory for Conservation, Monteverde Cloud Forest Preserve and Tropical Science Center, Santa Elena, Puntarenas 5655-73, Costa Rica. e-mail: [EMAIL PROTECTED] Robert Puschendorf is in the School of Biology, University of Costa Rica, San Pedro de Montes de Oca, Costa Rica. e-mail: [EMAIL PROTECTED] Global warming is altering the distribution and abundance of plant and animal species. Application of a basic law of ecology predicts that many will vanish if temperatures continue to rise. Evidence that climate change is affecting life on Earth continues to mount1, 2. But how great is the threat to biodiversity? On page 145 of this issue, Thomas et al.3 show that global warming, projected to the year 2050, could sharply increase extinction probabilities for a sample of 1,103 species representing terrestrial regions from Mexico to Australia. If temperatures follow middle-of-the-road projections, the study suggests, about one-quarter of these species may disappear - a loss that would exceed that expected from habitat destruction. Thomas et al. assume that each species can persist only under a particular set of climatic conditions. This 'climate envelope', assessed by modelling current geographical distribution in relation to climatic gradients, serves to predict future distribution. As warming alters these gradients, many species are shifting towards the poles or to higher elevations, their ranges often contracting as the area of climatically suitable habitat declines1, 2. To predict the outcome, Thomas et al. turn to one of ecology's few ironclad laws: the species-area relationship. Basically, smaller areas support fewer species. In 1859, the year in which Darwin's Origin of Species appeared, H. C. Watson demonstrated this law for Britain's vascular flora by comparing sampling areas ranging from a square mile to all of England4. Plotting the logarithm of the number of species as a function of the logarithm of area, he found a linear relationship (Fig. 1). This pattern, we now know, is typical of regional scales, where a power-law equation usually describes the relationship between number of species and area4. At these scales, the species-area curve probably reflects the configuration of species' ranges and thus the history of speciation, dispersal and extinction. Figure 1 H. C. Watson's demonstration of the species-area law for Britain's vascular flora. Full legend High resolution image and legend (21k) Using this relationship to assess climate-related extinction risk, Thomas et al. explore three approaches. Their conclusions are the same with each of them. They consider change in area summed for the various species, proportional loss of area averaged across species, and change in area for each species individually. Averaging the results of these methods, applied under two dispersal scenarios, they estimate the extinction probability for different amounts of warming as 18% (0.8-1.7 ¡C), 24% (1.8-2.0 ¡C) and 35% (above 2.0 ¡C). These estimates might be optimistic. The risk of extinction increases as global warming interacts with other factors - such as landscape modification, species invasions and build-up of carbon dioxide - to disrupt communities and ecological interactions. Furthermore, the models might not capture some key climatic changes. One pillar of Thomas and colleagues' analysis is the modelling of range contractions in the tropical rainforests of northeast Australia5. But the authors of that study5 emphasize that it considers only the effects of rising temperatures and that other changes could magnify the impacts. In the highlands, for example, an increase in the altitudes at which clouds form6-8 could affect communities that require frequent immersion in clouds and mist. Changes in cloud cover might also be important. Warming accelerates evaporation and increases the air's capacity to hold water, thereby increasing its content of water vapour9. Cloud formation, however, depends on relative humidity, which varies inversely with temperature, so warming may reduce cloudiness over some regions. In contrast, where air masses cool sufficiently - for instance where they ascend mountain slopes - increased water vapour should translate into enhanced cloud formation, even if condensation begins at increased altitudes. Accordingly, widespread increases in cloud cover are under way9. Are changing cloud patterns already contributing to the extinction of species? Thomas et al.3 refer to amphibian declines and disappearances in the mountains of Costa Rica as the one example in which recent warming has been implicated in such losses (Fig. 2). Various biological changes in these mountains are associated with unusually dry weather attributed to an increase in heights of cloud formation6. Understanding amphibian extinctions is crucial, given that they are taking place in highlands around the world10, 11. For example, most of the 70-odd members of the harlequin frog genus Atelopus, endemic to Central and South America, have vanished or declined markedly (E. La Marca, personal communication). Figure 2 Absent amphibians. Full legend High resolution image and legend (48k) Nevertheless, few studies have examined how climatic changes might be linked to the immediate causes of these declines12, 13. The climate-envelope concept championed by Thomas et al. might help to shed light on one such cause - outbreaks of the chytrid fungus Batrachochytrium dendrobatidis14, 15. This lethal parasite of amphibian skin thrives under cool, moist conditions. In culture, it grows at 6-28 ¡C but dies at higher temperatures. Experiments with the Australian frog Litoria chloris16 show that elevated body temperatures, reached naturally by basking in the sun or seeking warm microenvironments, can rid the frogs of this fungus. The low humidity typical of warm microsites might likewise enhance frog survival. Both increased cloud cover and unusually dry weather might hamper these defences. In highland tropical forests, ambient air temperatures generally lie within the climate envelope of Batrachochytrium. But these forests include shaded and sunlit microhabitats. Under clear skies, temperatures in the latter can quickly exceed 30 ¡C, so an amphibian can 'escape' from this envelope. Under cloudy skies, however, microhabitat temperatures mirror ambient temperatures, making escape difficult. Dry conditions may have similar consequences: with limiting moisture, an amphibian might have to stay in cool, damp places. Although exploring these potential links between climate and recent extinctions is essential, the patterns implicating global warming in such losses attest to the urgency of Thomas and colleagues' principal recommendation3. Reducing the concentrations of greenhouse gases - and reducing them soon - could minimize this warming and hence the number of extinctions. The threat to life on Earth is not just a problem for the future. It is part of the here and now. References 1. Parmesan, C. & Yohe, G. Nature 421, 37-42 (2003). | Article | PubMed | ChemPort | 2. Root, T. L. et al. Nature 421, 57-60 (2003). | Article | PubMed | ISI | ChemPort | 3. Thomas, C. D. et al. Nature 427, 145-148 (2004). | Article | 4. Hubbell, S. P. The Unified Neutral Theory of Biodiversity and Biogeography (Princeton Univ. Press, 2001). 5. Williams, S. E., Bolitho, E. E. & Fox, S. Proc. R. Soc. Lond. B 270, 1887-1892 (2003). | Article | PubMed | ISI | 6. Pounds, J. A., Fogden, M. P. L. & Campbell, J. H. Nature 398, 611-615 (1999). | Article | ISI | ChemPort | 7. Still, C. J., Foster, P. N. & Schneider, S. H. Nature 398, 608-610 (1999). | Article | ISI | ChemPort | 8. Richardson, A. D., Denny, E. G., Siccama, T. G. & Lee, X. J. Clim. 16, 2093-2098 (2003). | Article | ISI | 9. Houghton, J. T. et al. Climate Change 2001: The Scientific Basis (Cambridge Univ. Press, 2001). 10. Alford, R. A. & Richards, S. J. Annu. Rev. Ecol. Syst. 30, 133-165 (1999). | Article | ISI | 11. Ron, S. R., Duellman, W. E., Coloma, L. A. & Bustamante, M. R. J. Herpetol. 37, 116-126 (2003). | ISI | 12. Kiesecker, J. M., Blaustein, A. R. & Belden, L. K. Nature 410, 81-84 (2001). | Article | PubMed | ISI | ChemPort | 13. Pounds, J. A. Nature 410, 639-640 (2001). | Article | PubMed | ISI | ChemPort | 14. Berger, L. et al. Proc. Natl Acad. Sci. USA 95, 9031-9036 (1998). | Article | PubMed | ChemPort | 15. Burrowes, P. A., Joglar, R. L. & Greene, D. E. Herpetologica (in the press). 16. Woodhams, D. C., Alford, R. A. & Marantelli, G. Dis. Aquat. Org. 55, 65-67 (2003). | PubMed | ISI | Biofuel at Journey to Forever: http://journeytoforever.org/biofuel.html Biofuels list archives: http://archive.nnytech.net/index.php?list=biofuel Please do NOT send Unsubscribe messages to the list address. To unsubscribe, send an email to: [EMAIL PROTECTED] Yahoo! Groups Links To visit your group on the web, go to: http://groups.yahoo.com/group/biofuel/ To unsubscribe from this group, send an email to: [EMAIL PROTECTED] Your use of Yahoo! Groups is subject to: http://docs.yahoo.com/info/terms/