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Abstract Pollen protein content has been demonstrated to be an essential nutritional component for bees and thus important in mediating plant–pollinator interactions. However, little is known on the drivers and consequences of among‐species variation in pollen protein content and how this can impact male and female reproductive success across plant species. Among‐species variation in resources allocated to pollen nutrition could further be constrained by life‐history strategies (e.g. survival‐reproduction trade‐offs) or evolutionary history.Here, we surveyed pollen protein content for 29 species within a diverse co‐flowering community and evaluated the effect of pollen protein on male and female reproductive success. We also tested the role of life history (annuals vs. perennials) and phylogeny in mediating differences in resource allocation to pollen nutrition.We found that pollen protein content influences components of male (bee visitor abundance and pollen dispersal) but not female (conspecific pollen deposition and pollen tube growth) reproductive success, suggesting this trait affects plants only via male function. This sex‐specific effect further suggests the potential for sexual conflicts driven by differential investment on this trait. We found no phylogenetic signal on pollen protein content. However, pollen protein content was higher in annual compared to perennial species suggesting survival versus reproduction trade‐offs also contribute to variation in pollen protein at the community level.Our study underscores the importance of understanding the ecological and evolutionary drivers of pollen protein content across plant species. Our results further suggest the existence of sexual conflicts and ecological trade‐offs mediated by differential investment in pollen nutritional quality, with important implications for community assembly and the structure of plant–pollinator interactions. Read the freePlain Language Summaryfor this article on the Journal blog.
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Female reproduction and viral infection in a long‐lived mammal
Abstract For energetically limited organisms, life‐history theory predicts trade‐offs between reproductive effort and somatic maintenance. This is especially true of female mammals, for whom reproduction presents multifarious energetic and physiological demands.Here, we examine longitudinal changes in the gut virome (viral community) with respect to reproductive status in wild mature female chimpanzeesPan troglodytes schweinfurthiifrom two communities, Kanyawara and Ngogo, in Kibale National Park, Uganda.We used metagenomic methods to characterize viromes of individual chimpanzees while they were cycling, pregnant and lactating.Females from Kanyawara, whose territory abuts the park's boundary, had higher viral richness and loads (relative quantity of viral sequences) than females from Ngogo, whose territory is more energetically rich and located farther from large human settlements. Viral richness (total number of distinct viruses per sample) was higher when females were lactating than when cycling or pregnant. In pregnant females, viral richness increased with estimated day of gestation. Richness did not vary with age, in contrast to prior research showing increased viral abundance in older males from these same communities.Our results provide evidence of short‐term physiological trade‐offs between reproduction and infection, which are often hypothesized to constrain health in long‐lived species.
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- Award ID(s):
- 1926737
- PAR ID:
- 10478770
- Publisher / Repository:
- British Ecological Society
- Date Published:
- Journal Name:
- Journal of Animal Ecology
- Volume:
- 91
- Issue:
- 10
- ISSN:
- 0021-8790
- Page Range / eLocation ID:
- 1999 to 2009
- Format(s):
- Medium: X
- Sponsoring Org:
- National Science Foundation
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Abstract Seasonal changes in reproduction have been described for many taxa. As reproductive seasons progress, females often shift from greater energetic investment in many small offspring towards investing less total energy into fewer, better provisioned (i.e. larger) offspring. The underlying causes of this pattern have not been assessed in many systems.Two primary hypotheses have been proposed to explain these patterns. The first is an adaptive hypothesis from life‐history theory: early offspring have a survival advantage over those produced later. Accordingly, selection favours females that invest in offspring quantity early in the season and offspring quality later. The second hypothesis suggests these patterns are not intrinsic but result from passive responses to seasonal changes in the environment experienced by reproducing females (i.e. maternal environment).To disentangle the causes underlying this pattern, which has been reported in brown anole lizards (Anolis sagrei), we performed complementary field and laboratory studies. The laboratory study carefully controlled maternal environments and quantified reproductive patterns throughout the reproductive season for each female. The field study measured similar metrics from free ranging lizards across an entire reproductive season.In the laboratory, females increased relative effort per offspring as the reproductive season progressed; smaller eggs were laid earlier, larger eggs were laid later. Moreover, we observed significant among‐individual variation in seasonal changes in reproduction, which is necessary for traits to evolve via natural selection. Because these patterns consistently emerge under controlled laboratory conditions, they likely represent an intrinsic and potentially adaptive adjustment of reproductive effort as predicted by life‐history theory.The field study revealed similar trends, further suggesting that intrinsic patterns observed in the laboratory are strong enough to persist despite the environmental variability that characterizes natural habitats. The observed patterns are indicative of an adaptive seasonal shift in parental investment in response to a deteriorating offspring environment: allocating greater resources to late‐produced offspring likely enhances maternal fitness.more » « less
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- Free Publicly Accessible Full Text
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Accepted Manuscript1.0
- Journal Article:
- https://doi.org/10.1111/1365-2656.13799
