The importance of the Andes in the evolutionary radiation of Sigmodontinae (Rodentia, Cricetidae), the most diverse group of mammals in the Neotropics.

The Andean mountains stand out for their striking species richness and endemicity that characterize many emblematic Neotropical clades distributed in or around these mountains. The radiation of the Sigmodontinae subfamily, the most diversified mammalian group in the Neotropics, has been historically related to Andean orogenesis. We aim to evaluate this interplay between geological processes and biological responses through the diversification dynamics, the biogeographical history, and the range evolution of the subfamily. For these, we built the most comprehensive phylogeny and gathered 14,836 occurrences for the subfamily. We identified one shift in the speciation rate in the genus Akodon, which suffered their Andean radiation after the arrival of non-Andean ancestors. Our biogeographic analyses show multiple dispersal paths throughout the evolution that allowed this subfamily to colonize all Neotropics. The Northern Andes and Central-Southern Andes were the most important sources of diversity. In addition, the Central-Southern Andes were the most relevant sink, receiving the highest number of lineages. The Andean region exhibited higher speciation and turnover rates than non-Andean regions. Thus, our results support the crucial role of the Andean Mountains in the Sigmodontinae radiation, acting as a "macroevolutionary cradle" and "species attractor" for several sigmodontine lineages at different times, and as a "species pump" becoming the biogeographic source of multiple widely distributed neotropical lineages. Then, complex macroevolutionary dynamics would explain these rodents' high extant Andean diversity and their wide distribution in the Neotropics.

Coprophagous Insects and the Ecology of Infectious Diseases of Wildlife.

A diversity of macro- and microparasitic species exert strong influences on wildlife population density, community structure, and ecosystem functioning, all through their impacts on individual host fitness. Through consuming, manipulating, and relocating wildlife feces, over 7,000 species of coprophagous dung beetles interact with a staggering diversity of wildlife parasites with fecal-oral transmission in ways that both increase and decrease transmission. Here, we review the mechanisms by which dung beetles influence micro- and macroparasite transmission and outline a future research framework that integrates theory and empirical insights to advance our understanding of how these relationships may interact with ongoing environmental change drivers to further influence wildlife populations and community structure. Any organism that significantly influences parasite transmission will impact multiple levels of biological organization. Therefore, improving our understanding of the role of dung beetle interactions within disease ecology will be key to future efforts to understand the overall dynamics of infection in wildlife and how parasites contribute to the maintenance of ecosystem structure and function and evolutionary processes in wild animals.