its width (32). On physical grounds, the thin gas gap suggested by our measurements should also be expected to possess soft modes with fluctuations whose wavelength ranges from small to large. From this perspective, we then expect that the experimental geometry of a Janus-type water film, selected for experimental convenience, was incidental to the main physical effect.These conclusions have evident connections to understanding the long-standing question of the structure of aqueous films near a hydrophobic surface and may have a bearing on understanding the structure of water films near the patchy hydrophilichydrophobic surfaces that are so ubiquitous in nature.Note added in proof: We have recently been made aware of neutron reflectivity experiments that indicate the existence of a nanometer-thick vapor-like coating that forms on an extended hydrophobic surface when it is immersed in water (33, 34). The high alpha-diversity of tropical forests has been amply documented, but beta-diversity-how species composition changes with distance-has seldom been studied. We present quantitative estimates of beta-diversity for tropical trees by comparing species composition of plots in lowland terra firme forest in Panama, Ecuador, and Peru. We compare observations with predictions derived from a neutral model in which habitat is uniform and only dispersal and speciation influence species turnover. We find that beta-diversity is higher in Panama than in western Amazonia and that patterns in both areas are inconsistent with the neutral model. In Panama, habitat variation appears to increase species turnover relative to Amazonia, where unexpectedly low turnover over great distances suggests that population densities of some species are bounded by as yet unidentified processes. At intermediate scales in both regions, observations can be matched by theory, suggesting that dispersal limitation, with speciation, influences species turnover. References and NotesBeta-diversity is central to concepts about what controls diversity in ecological communities. Species turnover can reflect deterministic processes, such as species' adaptations to differences in climate or substrate, or it can result from limited dispersal coupled with speciation, delayed response to climatic change, or other historical effects. Perhaps more important, beta-diversity is as important as alpha-diversity for conservation, because species turnover influences diversity at large scales. Recently, Hubbell (1) and Harte et al. (2, 3) have derived theories relating species turnover with distance to species-area relations and total species richness. In very rich forests of the neotropics, these theories may allow us to interpolate species turnover and estimate species distributions and diversity at scales relevant to conservation even with the sparse data from forest plots that are currently available.To measure beta-diversity and test factors influencing it, we identified all trees in 34 plots near the Panama Canal, 16 plots in Ecuador's Yasuní National Park, and 1...

Summary 1We mapped and identified all trees ≥ 10 mm in diameter in 25 ha of lowland wet forest in Amazonian Ecuador, and found 1104 morphospecies among 152 353 individuals. The largest number of species was mid-sized canopy trees with maximum height 10-20 m and understorey treelets with maximum height of 5-10 m. 2 Several species of understorey treelets in the genera Matisia and Rinorea dominated the forest numerically, while important canopy species were Iriartea deltoidea and Eschweilera coriacea . 3 We examined how species partition local topographic variation into niches, and how much this partitioning contributes to forest diversity. Evidence in favour of topographic niche-partitioning was found: similarity in species composition between ridge and valley quadrats was lower than similarity between two valley (or two ridge) quadrats, and 25% of the species had large abundance differences between valley and ridge-top. On the other hand, 25% of the species were generalists, with similar abundance on both valley and ridges, and half the species had only moderate abundance differences between valley and ridge. 4 Topographic niche-partitioning was not finely grained. There were no more than three distinct vegetation zones: valley, mid-slope, and upper-ridge, and the latter two differed only slightly in species composition. 5 Similarity in species composition declined with distance even within a topographic habitat, to about the same degree as it declined between habitats. This suggests patchiness not related to topographic variation, and possibly due to dispersal limitation. 6 We conclude that partitioning of topographic niches does make a contribution to the α -diversity of Amazonian trees, but only a minor one. It provides no explanation for the co-occurrence of hundreds of topographic generalists, nor for the hundreds of species with similar life-form appearing on a single ridge-top.

BackgroundThe threats facing Ecuador's Yasuní National Park are emblematic of those confronting the greater western Amazon, one of the world's last high-biodiversity wilderness areas. Notably, the country's second largest untapped oil reserves—called “ITT”—lie beneath an intact, remote section of the park. The conservation significance of Yasuní may weigh heavily in upcoming state-level and international decisions, including whether to develop the oil or invest in alternatives.Methodology/Principal FindingsWe conducted the first comprehensive synthesis of biodiversity data for Yasuní. Mapping amphibian, bird, mammal, and plant distributions, we found eastern Ecuador and northern Peru to be the only regions in South America where species richness centers for all four taxonomic groups overlap. This quadruple richness center has only one viable strict protected area (IUCN levels I–IV): Yasuní. The park covers just 14% of the quadruple richness center's area, whereas active or proposed oil concessions cover 79%. Using field inventory data, we compared Yasuní's local (alpha) and landscape (gamma) diversity to other sites, in the western Amazon and globally. These analyses further suggest that Yasuní is among the most biodiverse places on Earth, with apparent world richness records for amphibians, reptiles, bats, and trees. Yasuní also protects a considerable number of threatened species and regional endemics.Conclusions/SignificanceYasuní has outstanding global conservation significance due to its extraordinary biodiversity and potential to sustain this biodiversity in the long term because of its 1) large size and wilderness character, 2) intact large-vertebrate assemblage, 3) IUCN level-II protection status in a region lacking other strict protected areas, and 4) likelihood of maintaining wet, rainforest conditions while anticipated climate change-induced drought intensifies in the eastern Amazon. However, further oil development in Yasuní jeopardizes its conservation values. These findings form the scientific basis for policy recommendations, including stopping any new oil activities and road construction in Yasuní and creating areas off-limits to large-scale development in adjacent northern Peru.

Most ecological hypotheses about species coexistence hinge on species differences, but quantifying trait differences across species in diverse communities is often unfeasible. We examined the variation of demographic traits using a global tropical forest data set covering 4500 species in 10 large-scale tree inventories. With a hierarchical Bayesian approach, we quantified the distribution of mortality and growth rates of all tree species at each site. This allowed us to test the prediction that demographic differences facilitate species richness, as suggested by the theory that a tradeoff between high growth and high survival allows species to coexist. Contrary to the prediction, the most diverse forests had the least demographic variation. Although demographic differences may foster coexistence, they do not explain any of the 16-fold variation in tree species richness observed across the tropics. C omparative studies of tree demography typically consider the entire community as a unit, ignoring species differences (1), simply because most tree inventories include small samples of many species (2, 3). Comparative studies show that tropical forests typically have higher turnover than do temperate forests (4) and that higher tree turnover associates with higher tree diversity (5). These studies cannot, however, test ecological hypotheses about diversity, coexistence, and demography (6-10).A tradeoff between rapid growth and long life span permits species coexistence and can foster diversity: Species reproducing early in life persist despite poor competitive ability by growing rapidly on disturbed sites where resources are abundant. Long-lived species coexist by outliving the weedy invaders, persisting where resources are scarce. This is a familiar and widely known tradeoff in plant and animal communities (9-11) called the successionalniche hypothesis (7,12). At a deterministic equilibrium, an indefinite number of species can coexist by this mechanism, each differing from all others along a continuum from short life span (with high growth) to long life span (and low growth). With stochastic demography, however, there is limiting similarity and the equilibrium species richness is finite (11, 13). This hypothesis is widely quoted as an explanation for tropical forest diversity (14-16). Here, we ask whether species differences along a demographic axis explain why some tropical forests have many more species than others.If demographic niches are a key force controlling forest diversity, then more diverse forests have more demographic niches. More niches could come about either by spreading demographic rates over a wider range or packing more in the same range. Here, we focus on the first prediction: Tropical forests gain diversity by having a wider range of demographic niches, as reflected by the range of mortality and growth rates across species.We provide a direct test by quantifying mortality and growth of 4500 tree species in 10 different forests in America, Asia, and Africa (17). The 10 sites form a large-scale ob...