The food requirements of dependent sons and daughters have important implications for evolution of the sex ratio, according to current sex allocation theory. We studied food requirements of nestling American kestrels (Falco sparverius), a moderately size-dimorphic falcon, by hand-feeding 61 birds from hatching to fledging. Daughters, the larger gender, consumed 6.99% more food than did sons. Sons did not have higher energy expenditure from higher effort during sibling competition than daughters did, so parents must supply more food to satisfy daughters' needs than to satisfy sons'. A review of all related studies shows a strong positive association between the degree of sexual size dimorphism and gender difference in food requirements.
Genetic structure can be influenced by local adaptation to environmental heterogeneity and biogeographic barriers, resulting in discrete population clusters. Geographic distance among populations, however, can result in continuous clines of genetic divergence that appear as structured populations. Here, we evaluate the relevant importance of these three factors over a landscape characterized by environmental heterogeneity and the presence of a hypothesized biogeographic barrier in producing population genetic structure within 13 codistributed snake species using a genomic data set. We demonstrate that geographic distance and environmental heterogeneity across western North America contribute to population genomic divergence. Surprisingly, landscape features long thought to contribute to biogeographic barriers play little role in divergence community wide. Our results suggest that isolation by environment is the most important contributor to genomic divergence. Furthermore, we show that models of population clustering that incorporate spatial information consistently outperform nonspatial models, demonstrating the importance of considering geographic distances in population clustering. We argue that environmental and geographic distances as drivers of community‐wide divergence should be explored before assuming the role of biogeographic barriers.
Body size differences typically influence sibling competition among nestling birds. In many species hatching order determine nestling size rank; however, sexually dimorphic growth may confound this correlation, giving one sex a consistent competitive advantage and leading to differential survival of the sexes. We found that captive female American Kestrel (Falco sparverius) nestlings were larger than male sibling nestmates from shortly after hatchling through fledging. When food delivered by parents was small enough to be seized and swallowed immediately by a nestling, females showed clear competitive superiority over male sibling nestmates in scramble competition. Females also took larger portions than males of small, yet unmonopolizeable, items. Competitive ability and gender were unrelated when parents delivered large, unmonopolizeable prey. Choice experiments demonstrated that parent feeding preferences did not account for the females' advantage. Based on the above, we expected fledging sex ratio to become increasingly female biased as nestling mortality increased, because nestling mortality increases and prey size decreases when preferred prey (unmonopolizeable rodents) are not available. Data from a wild kestrel population in eastern Pennsylvania supported this prediction, showing a significant positive relationship between fledging brood size and representation of males in the brood, although we note an alternative explanation for this result. Female competitive dominance and its interaction with prey size may influence the evolution of sexual size dimorphism and primary sex ratio in this species and other raptors.
Here we describe Haemoproteus (Haemoproteus) multivolutinus n. sp. from a tambourine dove (Turtur timpanistria) of Uganda and Haemoproteus (Haemoproteus) paramultipigmentatus n. sp. (Haemosporida, Haemoproteidae) from the Socorro common ground dove (Columbina passerina socorroensis) of Socorro Island, Mexico. These parasites are described based on the morphology of their blood stages and segments of the mitochondrial cytochrome b gene that can be used for molecular identification and diagnosis of these species. Gametocytes of H. multivolutinus possess rod-like pigment granules and are evenly packed with volutin, which masks pigment granules and darkly stains both macro- and microgametocytes in the early stages of their development. Based on these 2 characters, H. multivolutinus can be readily distinguished from other species of hemoproteids parasitizing columbiform (Columbiformes) birds. Haemoproteus paramultipigmentatus resembles Haemoproteus multipigmentatus; it can be distinguished from the latter parasite primarily due to the broadly ovoid shape of its young gametocytes and significantly fewer pigment granules in its fully developed gametocytes. We provide illustrations of blood stages of the new species, and phylogenetic analyses identify DNA lineages closely related to these parasites. Cytochrome b lineages of Haemoproteus multivolutinus and H. paramultipigmentatus cluster with hippoboscid-transmitted lineages of hemoproteids; thus these parasites likely belong to the subgenus Haemoproteus. We emphasize the importance of using cytochrome b sequences in conjunction with thorough microscopic descriptions to facilitate future identification of these and other avian hemosporidian species.
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