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ABSTRACT Frugivore‐mediated seed dispersal drives ecological functioning across tropical forests. The biological mechanisms affecting seed dispersal outcomes, as well as the role of specific functional traits in plants and their dispersers, is still not well understood. To address this gap, we conducted germination experiments in eight species of captive and two species of wild lemurs, which disperse different plant species. We (1) quantified the effects of pulp removal, seed priming, and feces effects (nutrient/microbial fertilization) through gut passage as mechanisms, (2) determined the effect of frugivore species on germination, and (3) assessed how individual plant and animal traits affected two seed germination outcomes: success rates and time‐to‐germination. Accounting for phylogenetic non‐independence of plants and estimating phylogenetic signal, we evaluated the effects of lemur gut passage and functional traits in a Bayesian framework. Seed priming during gut passage was the primary mechanism through which lemurs improved germination rates and decreased time‐to‐germination. Gut passage influenced the effect of seed length on germination probability but not time‐to germination. Germination outcomes varied by disperser species and seed size. Furthermore, seeds passed by male lemurs were 40% more likely to germinate than those passed by female lemurs. Germination probability was more similar for closely related plant species compared to those that were more distantly related, while the plant phylogenetic effects on time‐to‐germination were weaker. Moreover, germination depended on experimental setting; for example, lemur gut passage decreased time‐to‐germination in captive, but not wild settings. Our results highlight the complexity of biological mechanisms determining seed dispersal outcomes; ecological and evolutionary factors were important drivers of germination. Considering a diversity of potential effects is critical for advancing a mechanistic understanding of species interactions and their outcomes. 

Small terrestrial mammals are major hosts of infectious agents responsible for zoonotic diseases. Astroviruses (AstVs)–the cause of non-bacterial gastroenteritis mainly affecting young children–have been detected in a wide array of mammalian and avian host species. However, understanding the factors that influence AstV infection within and across hosts is limited. Here, we investigated the impact of land use changes on AstVs in terrestrial small mammals in rural northeastern Madagascar. We sampled 515 small mammals, representing seven endemic and four introduced species. Twenty-two positive samples were identified, all but one of which were found in the introduced speciesMus musculusandRattus rattus(family Muridae), with a positivity rate of 7.7% (6/78) and 5.6% (15/266), respectively. The non-introduced rodent case was from an endemic shrew-tenrec (family Tenrecidae). We found the highest positivity rate of AstVs infection in brushy regrowth (17.5%, 7/40) as compared to flooded rice fields (4.60%, 8/174), secondary forest (4.1%, 3/74), agroforest (3.6%, 1/28), village (2.61%, 3/115), and semi-intact forest (0%, 0/84). A phylogenetic analysis revealed an association between AstVs and their rodent host species. None of the viruses were phylogenetically related to AstVs previously described in Malagasy bats. This study supports AstV circulation in synanthropic animals in agricultural habitats of Madagascar and highlights the need to assess the spillover risk to human populations in rural areas. 

Paleontological and neontological systematics seek to answer evolutionary questions with different datasets. Phylogenies inferred for combined extant and extinct taxa provide novel insights into the evolutionary history of life. Primates have an extensive, diverse fossil record and molecular data for living and extinct taxa are rapidly becoming available. We used two models to infer the phylogeny and divergence times for living and fossil primates, the tip-dating (TD) and fossilized birth-death process (FBD). We collected new morphological data, especially on the living and extinct endemic lemurs of Madagascar. We combined the morphological data with published DNA sequences to infer near-complete (88% of lemurs) time-calibrated phylogenies. The results suggest that primates originated around the Cretaceous-Tertiary boundary, slightly earlier than indicated by the fossil record and later than previously inferred from molecular data alone. We infer novel relationships among extinct lemurs, and strong support for relationships that were previously unresolved. Dates inferred with TD were significantly older than those inferred with FBD, most likely related to an assumption of a uniform branching process in the TD compared to a birth-death process assumed in the FBD. This is the first study to combine morphological and DNA sequence data from extinct and extant primates to infer evolutionary relationships and divergence times, and our results shed new light on the tempo of lemur evolution and the efficacy of combined phylogenetic analyses.