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Summary1. We analysed the relationships between species richness, island area, and habitat diversity for birds, bats, butter¯ies, and reptiles and amphibians on 19 islands in the Lesser Antilles. Habitat diversity was quanti®ed by Simpson's index based on the total areas of ®ve vegetation types on each island. Island area varied over two orders of magnitude (13±1510 km 2 ) and habitat diversity varied between 1 and 3´7 equivalents of equally abundant habitat types. 2. Because the Lesser Antilles consist of an inner arc of high, volcanic islands and an outer arc of low-lying islands formed of uplifted marine sediments, correlations between area and elevation (r 2 = 0´32) and between area and habitat diversity (r 2 = 0´40) were weak. Habitat diversity was, however, strongly correlated with maximum island elevation (r 2 = 0´85). 3. Simple correlations of species richness with island area were signi®cant for all four faunal groups, and simple correlations of species richness with elevation and habitat were signi®cant for all groups except bats. In multiple regressions of species richness on area and habitat diversity together, area was a signi®cant eect for birds and bats, and habitat diversity was a signi®cant eect for birds, butter¯ies, and reptiles and amphibians. 4. These results suggest that the four Lesser Antillean taxonomic groups dier in their responses to area and habitat diversity. For butter¯ies and for reptiles and amphibians, the relationship of species richness to area is probably a fortuitous consequence of a relationship between habitat diversity and area. Bird species richness responds independently to both habitat diversity and area, and bat species richness is in¯uenced by area but not by habitat diversity. 5. We suggest that this variation is related to dierences in several biological traits of the dierent faunal groups. Strong habitat-diversity eects are likely in taxa with high degrees of habitat specialization, populations large enough to have a low probability of stochastic extinction, life-cycles that include a resistant resting stage that reduces vulnerability to catastrophic extinction, or a combination of these traits. In contrast, strong area eects are likely in taxa with weak habitat specialization, low population density, or both. 6. At least in Lesser Antillean birds, it is unlikely that immigration depends on island size. Therefore, the species±area relationship for birds is probably generated by island-size-dependent extinction. Among the four taxonomic groups we studied, only butter¯ies are likely to show a`rescue eect' stemming from frequent between-island movement of individuals, as only butter¯ies exhibited low levels of endemism and lacked a unique area eect for species richness. 7. Considered in concert, these taxon-speci®c dierences demonstrate that both biological characteristics of organisms and geographical features of island groups mediate the relative contribution of island area and habitat diversity to variation in species richness.
Summary1. We analysed the relationships between species richness, island area, and habitat diversity for birds, bats, butter¯ies, and reptiles and amphibians on 19 islands in the Lesser Antilles. Habitat diversity was quanti®ed by Simpson's index based on the total areas of ®ve vegetation types on each island. Island area varied over two orders of magnitude (13±1510 km 2 ) and habitat diversity varied between 1 and 3´7 equivalents of equally abundant habitat types. 2. Because the Lesser Antilles consist of an inner arc of high, volcanic islands and an outer arc of low-lying islands formed of uplifted marine sediments, correlations between area and elevation (r 2 = 0´32) and between area and habitat diversity (r 2 = 0´40) were weak. Habitat diversity was, however, strongly correlated with maximum island elevation (r 2 = 0´85). 3. Simple correlations of species richness with island area were signi®cant for all four faunal groups, and simple correlations of species richness with elevation and habitat were signi®cant for all groups except bats. In multiple regressions of species richness on area and habitat diversity together, area was a signi®cant eect for birds and bats, and habitat diversity was a signi®cant eect for birds, butter¯ies, and reptiles and amphibians. 4. These results suggest that the four Lesser Antillean taxonomic groups dier in their responses to area and habitat diversity. For butter¯ies and for reptiles and amphibians, the relationship of species richness to area is probably a fortuitous consequence of a relationship between habitat diversity and area. Bird species richness responds independently to both habitat diversity and area, and bat species richness is in¯uenced by area but not by habitat diversity. 5. We suggest that this variation is related to dierences in several biological traits of the dierent faunal groups. Strong habitat-diversity eects are likely in taxa with high degrees of habitat specialization, populations large enough to have a low probability of stochastic extinction, life-cycles that include a resistant resting stage that reduces vulnerability to catastrophic extinction, or a combination of these traits. In contrast, strong area eects are likely in taxa with weak habitat specialization, low population density, or both. 6. At least in Lesser Antillean birds, it is unlikely that immigration depends on island size. Therefore, the species±area relationship for birds is probably generated by island-size-dependent extinction. Among the four taxonomic groups we studied, only butter¯ies are likely to show a`rescue eect' stemming from frequent between-island movement of individuals, as only butter¯ies exhibited low levels of endemism and lacked a unique area eect for species richness. 7. Considered in concert, these taxon-speci®c dierences demonstrate that both biological characteristics of organisms and geographical features of island groups mediate the relative contribution of island area and habitat diversity to variation in species richness.
Animal signals evolve by striking a balance between the need to convey information through particular habitats and the limitations of what types of signals can most easily be produced and perceived. Here, we present new results from field measures of undisturbed behavior and biochemical analyses of scent marks from 12 species of Sceloporus lizards to explore whether evolutionary changes in chemical composition are better predicted by measures of species behavior, particularly those associated with visual displays, chemoreception, and locomotion, or by measures of habitat climate (precipitation and temperature). We found that more active lizard species used fewer compounds in their volatile scent marks, perhaps conveying less specific information about individual and species identity. Scent marks from more active lizard species also had higher proportions of saturated fatty acids, and the evolution of these compounds has been tracking the phylogeny closely as we would expect for a metabolic byproduct. In contrast, the proportions of unsaturated fatty acids were better explained by evolutionary shifts in habitat temperature (and not precipitation), with species in warmer climates using almost no volatile unsaturated fatty acids. The proportion of aldehydes was explained by both behavior and environment, decreasing with behavioral activity and increasing with habitat temperature. Our results highlight the evolutionary flexibility of complex chemical signals, with different chemical compounds responding to different elements of the selective landscape over evolutionary time.
Home range of Aspidoscelis cozumela (Squamata: Teiidae): a parthenogenetic lizard microendemic to Cozumel Island, México. Home range is defined as the area within which an individual moves to acquire resources necessary to increase their fitness and may vary inter and intra-specifically with biotic and abiotic factors. This study details the home range of the parthenogenic lizard, Aspidoscelis cozumela, an active forager microendemic to Cozumel Island, México, with high preference for open sand beaches. The home range of A. cozumela was compared with other species of Aspidoscelis (gonochoric and parthenogenetic) and other lizards that occupy coastal habitats. Furthermore, the biotic and abiotic factors that may influence home range were analyzed. This study was conducted in the beach located on the East side of the island (area of 4 000 m 2 ) that is composed primarily of halophyte vegetation with high levels of sunlight. From 1999 to 2001, nine samples were taken which included the dry, rainy, "nortes", and breeding seasons. During each sampling, capture-mark-recapture techniques were conducted and the date, time of day, and snout-vent length (SVL) were recorded to the nearest millimeter. Individuals were located in the study area using a bi-coordinate reference using 10 x 10 m subdivisions of the habitat. Home range and home range overlap were calculated using the convex polygon method in McPaal and home range/SVL correlation was tested using Pearson´s correlation. To calculate females home range, three or more recaptures were considered. A total of 20 home ranges that averaged 45.1 ± 14.0 m 2 were obtained and no correlation between SVL and home range size was detected (p = 0.9229, n = 20). However, removing individuals with outlier home ranges (females with home ranges > 100 m 2 , n = 2) resulted in a positive correlation with SVL (r = 0.61, p = 0.0072, n = 18). A 22.9 ± 5.7% overlap in home range was also detected. The small home range of A. cozumela represents the smallest home range within the Aspidoscelis genus recorded to date (including both parthenogenetic and gonochoric species) and contrasts the theoretical predictions of broad home ranges for widely foraging species. Thermoregulatory benefits and a high population density may explain the small home range of A. cozumela. Although this species is highly adapted to the environmental conditions present on the open sand beaches, anthropogenic effects on these habitats by the development of tourism infrastructure may jeopardize their existence on Cozumel Island. Rev. Biol. Trop. 63 (3): 771-781. Epub 2015 September 01.
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