Search arXivSearch

arXiv · 2412.09062

The expensive son hypothesis

Abstract

In its initial form, the expensive son hypothesis postulates that sons from male-biased sexually dimorphic species require more food during growth than daughters, which ultimately incur fitness costs for mothers predominantly producing and rearing sons. We first dissect the evolutionary framework in which the expensive son hypothesis is rooted, and we provide a critical reappraisal of its differences from other evolutionary theories proposed in the field of sex allocation. Then, we synthesize the current (and absence of) support for the costs of producing and rearing sons on maternal fitness components (future reproduction and survival). Regarding the consequences in terms of future reproduction, we highlight that species with pronounced sexual size dimorphism display a higher cost of sons than of daughters on subsequent reproductive performance, at least in mammals. However, in most studies, the relative fitness costs of producing and rearing sons and daughters can be due to sex-biased maternal allocation strategies rather than differences in energetic demands of offspring, which constitutes an alternative mechanism to the expensive son hypothesis stricto sensu. We observe that empirical studies investigating the differential costs of sons and daughters on maternal survival in non-human animals remain rare, especially for long-term survival. Indeed, most studies have investigated the influence of offspring sex (or litter sex ratio) at year $T$ on survival at year $T+1$, and they rarely provide a support to the expensive son hypothesis. On the contrary, in humans, most studies have focused on the relationship between proportion of sons and maternal lifespan, but these results are inconsistent. Our study highlights new avenues for future research that should provide a comprehensive view of the expensive son hypothesis, by notably disentangling the effects of offspring behaviour from the effect of sex-specific maternal allocation. Moreover, we emphasize that future studies should also embrace the mechanistic side of the expensive son hypothesis, largely neglected so far, by deciphering the physiological pathways linking son's production to maternal health and fitness.

Explore related subjects

Keep this discovery

Explore connections, maps & timelines

BibTeXRIS

Lucas Invernizzi, Jean-françois Lemaître, Mathieu Douhard. 2024-12-12. The expensive son hypothesis. https://doi.org/10.1111/1365-2656.14207

Cite the original work for its findings. Save a collection to share your selection of sources.

KEEP EXPLORING

Related papers

Phase transitions in microbial lineage trees

Microbial populations exhibit high cell-to-cell variability, which fundamentally shapes population behavior. A striking consequence is the existence of phase transitions, where small genetic or environmental changes trigger abrupt shifts in population dynamics. While biological phase transitions have often been proposed, connecting observed behavior to the underlying physics has remained challenging. We combine population genetics with statistical physics to show how phase transitions arise naturally in microbial populations. We highlight the existence of a first-order transition in a model of bacterial plasmid engineering and find a strict lower bound on the number of plasmids that can be stably maintained in a population.

q-bio.PE

Phylogenetic Inference and the Stickiness of Fréchet Means, via Precise Asymptotics of an Embedded Random Walk

A well-known phenomenon in statistical analyses of populations of phylogenetic trees in the Billera-Holmes-Vogtmann space is that the topology of the Fréchet mean tree can contain multifurcations (i.e., internal nodes with more than two children), which raises the practical question of whether this reflects a population-level branching structure (hard polytomy) or merely sampling variability in the data (soft polytomy). This is an instance of the more general phenomenon of "stickiness" in non-Euclidean statistics, whereby the sample Fréchet mean in certain non-positively curved stratified spaces becomes permanently trapped in a lower-dimensional stratum. In this work, we identify a particular multidimensional random walk embedded within the Fréchet mean process, and we show that the time at which stickiness occurs is determined by the largest last-passage time above zero of the coordinates of this random walk. Using this representation, we develop a fully nonparametric procedure for estimating the probability that trifurcations in a sample Fréchet mean tree will bifurcate at some future time if more observations are collected. Lastly, we apply our methodology to a problem in phylogenetics where we consider whether an observed trifurcation in the species tree of primates, glires, and tree shrews is genuinely trifurcated at the population level.

q-bio.PE

Coexistence coalitions in propagule disperser quasi-communities

Many natural ecosystems harbor large numbers of coexisting species competing for far fewer distinct resources, in apparent defiance of the competitive exclusion principle. Various mechanisms have been proposed to explain this apparent paradox, often pertaining to organisms with a two-stage sessile--propagule life cycle. Here we develop a stochastic model class for such propagule disperser communities that combines competition--colonization trade-offs, spatial heterogeneity, demographic stochasticity, as well as inherited trait variation, and recover several classical models as special or limiting cases. Using bifurcation analysis, we classify equilibrium coalitions near the extinction threshold and give sufficient conditions for their realization by macroscopic equilibria away from the threshold, bypassing the costly numerical computation of the actual equilibrium states. Illustrative examples examine the resulting trait distributions and coalition patterns, demonstrating the interactive effects of different coexistence mechanisms.

q-bio.PE