First, local dispersive spatial interactions, with an underlying precipitation gradient, can reproduce the spatial aggregation of biomes with a stable savanna-forest boundary. Second, the boundary is determined not only by the amount of precipitation but also by the geometrical shape of the precipitation contours. These geometrical effects arise from continental-scale source-sink dynamics, which reproduce the mismatch between biome and climate. Dynamically, the spatial model predicts that dispersal may increase the resilience of tropical biome in response to global change the boundary continuously tracks climate, recovering following disturbances, unless the remnant biome patches are too small.Mating signals have evolved to attract target receivers, even to the point of exploiting receivers through perceptual manipulation. Signals, however, can also expose signalers to nontarget receivers, including predators and parasites, and thus have also evolved to decrease enemy attraction. Here we show that male tree frogs (Smilisca sila) reduce their attractiveness to eavesdropping enemies (bats and midges) by overlapping their calls at near-perfect synchrony with the calls of neighboring conspecifics. By producing calls that closely follow those of other males, synchronizing S. sila take advantage of an auditory illusion where enemies are more attracted to the leading call. Female S. sila, however, are less susceptible to this illusion. Thus, synchronization among signaling males can result in acoustic crypsis from predators without affecting female attraction. Given the widespread use of conspicuous mating signals and eavesdropping enemies, perceptual exploitation of eavesdroppers is likely a common driver of signal evolution.Evolution is never truly predictable, in part because the process of selection is recursive it operates on its own output to generate historical contingencies, so emergent traits can reshape how others evolve in the future. click here Studies rarely attempt to directly trace how recursion underlies present-day phenotypic pattern on a macroevolutionary basis. To address this gap, we examined how different selection regimes-each operating on a different timescale-guide the evolution of the woodpecker drum display. Approximately 200 species drum with distinctive speed and length, which are important for territorial competition. We discovered remarkable variation in drum rhythm, with some species drumming at constant rates and others changing speed along a range of mathematical functions. Rhythm undergoes divergent character displacement among sympatric sister species, a process that wanes as other reproductive boundaries emerge over time. Tracing the recursive effects of this process, we found that modifying rhythm may then potentiate or constrain speed/length elaboration. Additionally, increased sexual size dimorphism predicts the emergence of rhythms associated with constrained evolutionary rates of speed/length, implying that selection can also constrain itself. Altogether, our findings illustrate how recursion introduces contingencies that allow diverse phenotypes to arise from similar selection regimes.Inclusive fitness theory predicts that individuals can increase their indirect fitness by grouping with kin. However, kin grouping also increases competition between kin, which potentially outweighs its benefits. The level of kin competition is contingent on environmental conditions and thus highly variable. Hence, individuals should benefit from plastically adjusting kin discrimination according to the expected level of kin competition. Here, we investigate whether perceived high competition affects juvenile kin-shoaling preferences in the cichlid Pelvicachromis taeniatus. Juveniles were given the choice between two shoals consisting of either kin or nonkin. Levels of perceived competition were manipulated through food limitation in the face of the differential energy expenditure of differently sized fish. The preference to shoal with kin decreased with increasing levels of perceived competition; small food-deprived individuals avoided kin. Shoaling with kin under strong competition may reduce individual indirect fitness. Hence, individuals can likely improve their inclusive fitness by plastically adjusting their kin-grouping preferences.Blood oxygen-carrying capacity is one of the important determinants of the amount of oxygen supplied to the tissue per unit time and plays a key role in oxidative metabolism. In wild vertebrates, blood oxygen-carrying capacity is most commonly measured with the total blood hemoglobin concentration (Hb) and hematocrit (Hct), which is the volume percentage of red blood cells in blood. Here, I used published estimates of avian Hb and Hct (nearly 1,000 estimates from 300 species) to examine macroevolutionary patterns in the oxygen-carrying capacity of blood in birds. Phylogenetically informed comparative analysis indicated that blood oxygen-carrying capacity was primarily determined by species distribution (latitude and elevation) and morphological constraints (body mass). I found little support for the effect of life-history components on blood oxygen-carrying capacity except for a positive association of Hct with clutch size. Hb was also positively associated with diving behavior, but I found no effect of migratoriness on either Hb or Hct. Fluctuating selection was identified as the major force shaping the evolution of blood oxygen-carrying capacity. The results offer novel insights into the evolution of Hb and Hct in birds, and they provide a general, phylogenetically robust support for some long-standing hypotheses in avian ecophysiology.Variation in species richness across environmental gradients results from a combination of historical nonequilibrium processes (time, speciation, extinction) and present-day differences in environmental carrying capacities (i.e., ecological limits affected by species interactions and the abundance and diversity of resources). In a study of bird richness along the subtropical east Himalayan elevational gradient, we test the prediction that species richness patterns are consistent with ecological limits using data on morphology, phylogeny, elevational distribution, and arthropod resources. Species richness peaks at midelevations. Occupied morphological volume is roughly constant from low elevations to midelevations, implying that more species are packed into the same space at midelevations compared with low elevations. However, variance in beak length and differences in beak length between close relatives decline with elevation, which is a consequence of the addition of many small insectivores at midelevations.click here