Global climate change is known to affect the assembly of ecological communities by altering species' spatial distribution patterns, but little is known about how climate change may affect community assembly by changing species' temporal co-occurrence patterns, which is highly likely given the widely observed phenological shifts associated with climate change. Here, we analyzed a 29-year phenological data set comprising community-level information on the timing and span of temporal occurrence in 11 seasonally occurring animal taxon groups from 329 local meteorological observatories across China. We show that widespread shifts in phenology have resulted in community-wide changes in the temporal overlap between taxa that are dominated by extensions, and that these changes are largely due to taxa's altered span of temporal occurrence rather than the degree of synchrony in phenological shifts. Importantly, our findings also suggest that climate change may have led to less phenological mismatch than generally presumed, and that the context under which to discuss the ecological consequences of phenological shifts should be expanded beyond asynchronous shifts.
Cooperative breeding is a form of breeding system where in addition to a core breeding pair, one or more usually non-breeding individuals provide offspring care. Cooperative breeding is widespread in birds, but its origin and maintenance in contemporary populations are debated. Although deviations in adult sex ratio (ASR, the proportion of males in the adult population) have been hypothesized to influence the occurrence of cooperative breeding because of the resulting surplus of one sex and limited availability of breeding partners, this hypothesis has not been tested across a wide range of taxa. By using data from 188 bird species and phylogenetically controlled analyses, we show that cooperatively breeding species have more male-biased ASRs than non-cooperative species. Importantly, ASR predicts helper sex ratio: in species with more male-biased ASR, helper sex ratio is also more male biased. We also show that offspring sex ratios do not predict ASRs, so that the skewed ASRs emerge during the period when individuals aim to obtain a breeding position or later during adulthood. In line with this result, we found that ASR (among both cooperatively and non-cooperatively breeding species) is inversely related to sex bias in dispersal distance, suggesting that the cost of dispersal is more severe for the further-dispersing sex. As females usually disperse further in birds, this explains the generally male-biased ASR, and in combination with benefits of philopatry for males, this probably explains why ASR is more biased in cooperatively breeding species. Taken together, our results suggest that a sex bias in helping in cooperatively breeding species relates to biased ASRs. We propose that this relationship is driven by sex-specific costs and benefits of dispersal and helping, as well as other demographic factors. Future phylogenetic comparative and experimental work is needed to establish how this relationship emerges.This article is part of the themed issue 'Adult sex ratios and reproductive decisions: a critical re-examination of sex differences in human and animal societies'.
In many animal species, parents provide care for their offspring, but the parental roles of the two sexes differ considerably between and within species. Here, we use an individual-based simulation approach to investigate the evolutionary emergence and stability of parental roles. Our conclusions are in striking contrast to the results of analytical models. In the absence of initial differences between the sexes, our simulations do not predict the evolution of egalitarian care, but either female-biased or male-biased care. When the sexes differ in their pre-mating investment, the sex with the highest investment tends to evolve a higher level of parental care; this outcome does not depend on non-random mating or uncertainty of paternity. If parental investment evolves jointly with sexual selection strategies, evolution results in either the combination of female-biased care and female choosiness or in male-biased care and the absence of female preferences. The simulations suggest that the parental care pattern drives sexual selection, and not vice versa. Finally, our model reveals that a population can rapidly switch from one type of equilibrium to another one, suggesting that parental sex roles are evolutionarily labile. By combining simulation results with fitness calculations, we argue that all these results are caused by the emergence of individual variation in parental care strategies, a factor that was hitherto largely neglected in sex-role evolution theory.
In animals, species differ remarkably in parental care strategies. For instance, male-only care is prevalent in teleost fishes, while biparental care predominates in birds and female-only care is widespread in mammals. Understanding the origin and maintenance of diversified parental care systems is a key challenge in evolutionary ecology. It has been suggested that ecological factors and life-history traits play important roles in the evolution of parental care, but the generality of these predictions has not been investigated across a broad range of taxa. Using phylogenetic comparative analyses and detailed parental care data from 1101 avian species that represent 119 families of 26 orders, here we investigate whether parental strategies are associated with ecological variables (i.e., food type, nest structure, and coloniality) and life-history characteristics (i.e., chick development mode and body size). We show that parental care strategies are in relation to coloniality (solitary, semi-colonial, colonial) and chick development mode (altricial vs. precocial). Colonial and altricial species provide more biparental care than solitary and precocial species, respectively. In contrast, food type (plant, invertebrate, vertebrate), nest structure (open vs. closed), and body size do not covary systematically with parental care patterns in birds. Taken together, our results suggest that living in groups and/or having high-demand offspring are strongly associated with biparental care. Towards the end, we discuss future research directions for the study of parental care evolution. Significance statementAnimal species differ remarkably in the amount of care parents provide to their offspring and in the distribution of care tasks over the parents. In birds, for example, the young of some species are quite independent from the start, while the young of other species are helpless after hatching, requiring a lot of care. Moreover, either the female or the male does most of the caring in some species, while the parental tasks are shared equally in still other species. To understand the diversified parental care patterns, we applied advanced comparative methods to a large data set comprising over 1000 bird species. The analysis reveals that the parents tend to share their care duties equally when they live in groups and/or have offspring that are born helpless, and that parental care patterns are not associated with diet, nest type or body size. Hence, living in groups and having high-demand offspring seem to play important roles in the evolution of parental care.
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