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Esselstyn, J. A.

Publications and source records attributed to Esselstyn, J. A..

3 recordsLinked to original sources

Molecular evolution of male reproduction across species with highly divergent sperm morphology in diverse murine rodents

It remains unclear how variation in the intensity of sperm competition shapes phenotypic and molecular evolution across clades. Mice and rats in the subfamily Murinae are a rapid radiation exhibiting incredible diversity in sperm morphology and production. We combined phenotypic and genomic data to perform phylogenetic comparisons of male reproductive traits and genes across 78 murine species. We identified several shifts towards smaller relative testes mass, presumably reflecting reduced sperm competition. Several sperm traits were associated with relative testes mass, suggesting that mating system evolution selects for convergent suites of traits related to sperm competitive ability. We predicted that sperm competition would also drive more rapid molecular divergence in species with large testes. Contrary to this, we found that many spermatogenesis genes evolved more rapidly in species with smaller relative testes mass due to relaxed purifying selection. While some reproductive genes evolved rapidly under recurrent positive selection, relaxed selection played a greater role in underlying rapid evolution in small testes species. Our work demonstrates that postcopulatory sexual selection can impose strong purifying selection shaping the evolution of male reproduction, and that broad patterns of molecular evolution may help identify genes that contribute to male fertility.

evolutionary biology↗

Trait-specific patterns of community ecospace occupancy in an insular mammal radiation

Communities that occupy similar environments but vary in the richness of closely related species can illuminate how functional variation and species richness interact to fill ecological space in the absence of abiotic filtering, though this has yet to be explored on an oceanic island where the processes of community assembly may differ from continental settings. In discrete montane communities on the island of Sulawesi, local murine rodent (rats and mice) richness ranges from 7 to 23 species. We measured 17 morphological, ecological, and isotopic traits, both individually and grouped into 5 multivariate traits in 40 species, to test for the expansion or packing of functional space among nine murine communities. We employed a novel probabilistic approach for integrating intraspecific and community-level trait variance into functional richness. Trait-specific and phylogenetic diversity patterns indicate dynamic community assembly due to variable niche expansion and packing on multiple niche axes. Locomotion and covarying traits such as tail length emerged as a fundamental axis of ecological variation, expanding functional space and enabling the niche packing of other traits such as diet and body size. Though trait divergence often explains functional diversity in island communities, we found that phylogenetic diversity facilitates functional space expansion in some conserved traits such as cranial shape, while more labile traits are overdispersed both within and between island clades, suggesting a role of niche complementarity. Our results evoke interspecific interactions, differences in trait lability, and the independent evolutionary trajectories of each of Sulawesis 6 murine clades as central to generating the exceptional functional diversity and species richness in this exceptional, insular radiation.

ecology↗

Ecological causes of uneven diversification and richness in the mammal tree of life

The uneven distributions of species over geography (e.g., tropical versus temperate regions) and phylogeny (e.g., rodents and bats versus the aardvark) are prominent biological patterns for which causal interconnections remain enigmatic. Here we investigate this central issue for living mammals using time-sliced clades sampled from a comprehensive recent phylogeny (N=5,911 species, [~]70% with DNA) to assess how different levels of unsampled extinction impact the inferred causes of species richness variation. Speciation rates are found to strongly exceed crown age as a predictor of clade species richness at every time slice, rejecting a clock-like model in which the oldest clades are the most speciose. Instead, mammals that are low-vagility or daytime-active show the fastest recent speciation and greatest extant richness. This suggests primary roles for dispersal limitation leading to geographic speciation (peripatric isolation) and diurnal adaptations leading to ecological speciation (time partitioning). Rates of speciation are also faster in temperate than tropical lineages, but only among older clades, consistent with the idea that many temperate lineages are ephemeral. These insights, enabled by our analytical framework, offer straightforward support for ecological effects on speciation-rate variation among clades as the primary cause of uneven phylogenetic richness patterns.

evolutionary biology↗