Uncategorized

Ross L, Davies NG & Gardner A (in press) How to make a haploid male. Evolution Letters.

Haplodiploidy has evolved repeatedly among invertebrates, and appears to be associated with inbreeding. Evolutionary biologists have long debated the possible benefits for females in diplodiploid species to produce haploid sons–beginning their population’s transition to haplodiploidy–and whether inbreeding promotes or inhibits this transition. However, little attention has been given to what makes a haploid individual male rather than female, and whether the mechanism of sex determination may modulate the costs and benefits of male haploidy. We remedy this by performing a theoretical analysis of the origin and invasion of male haploidy across the full range of sex‐determination mechanisms and sib‐mating rates. We find that male haploidy is facilitated by three different mechanisms of sex determination–all involving male heterogamety–and impeded by the others. We also find that inbreeding does not pose an obvious evolutionary barrier, on account of a previously neglected sex‐ratio effect whereby the production of haploid sons leads to an abundance of granddaughters that is advantageous in the context of inbreeding. We find empirical support for these predictions in a survey of sex determination and inbreeding across haplodiploids and their sister taxa.

I am advertising three 4-year Research Fellow positions in the area of social evolution theory (details here). The project is very flexible and will be tailored to the skills, experience and interests of the assembled team. The application deadline is 28 Feb 2019.

Faria GS, Varela SAM & Gardner A (2019) The social evolution of sleep: sex differences, intragenomic conflicts and clinical pathologies. Proceedings of the Royal Society of London Series B — Biological Sciences 286, 20182188.

Sleep appears to be essential for most animals, including humans. Accordingly, individuals who sacrifice sleep are expected to incur costs and so should only be evolutionarily favoured to do this when these costs are offset by other benefits. For instance, a social group might benefit from having some level of wakefulness during the sleeping period if this guards against possible threats. Alternatively, individuals might sacrifice sleep in order to gain an advantage over mate competitors. Here, we perform a theoretical analysis of the social evolutionary pressures that drive investment into sleep versus wakefulness. Specifically, we: investigate how relatedness between social partners may modulate sleeping strategies, depending upon whether sleep sacrifice is selfish or altruistic; determine the conditions under which the sexes are favoured to adopt different sleeping strategies; identify the potential for intragenomic conflict between maternal-origin versus paternal-origin genes regarding an individual’s sleeping behaviour; translate this conflict into novel and readily testable predictions concerning patterns of gene expression; and explore the concomitant effects of different kinds of mutations, epimutations, and uniparental disomies in relation to sleep disorders and other clinical pathologies. Our aim is to provide a theoretical framework for future empirical data and stimulate further research on this neglected topic.

Dyble M, Gardner A, Vinicius L & Migliano AB (2018) Inclusive fitness for in-laws. Biology Letters 14, 20180515.Cooperation among kin is common across the natural world and can be explained in terms of inclusive fitness theory, which holds that individuals can derive indirect fitness benefits from aiding genetically related individuals. However, human kinship includes not only genetic kin but also kin by marriage: our affines (in-laws) and spouses. Can cooperation between these genetically unrelated kin be reconciled with inclusive fitness theory? Here, we argue that although affinal kin and spouses do not necessarily share genetic ancestry, they may have shared genetic interests in future reproduction and, as such, can derive indirect fitness benefits though cooperating. We use standard inclusive fitness theory to derive a coefficient of shared reproductive interest (s) that predicts altruistic investment both in genetic kin and in spouses and affines. Specifically, a behaviour that reduces the fitness of the actor by c and increases the fitness of the recipient by b will be favoured by natural selection when sb > c. We suggest that the coefficient of shared reproductive interest may provide a valuable tool for understanding not only the evolution of human kinship but also cooperation and conflict across the natural world more generally.

I am offering a fully-funded, 3.5 year PhD studentship on “Theory of social evolution” (details here). The application deadline is 2 Dec 2018.

Micheletti AJC, Ruxton GD & Gardner A (2018) Why war is a man’s game. Proceedings of the Royal Society of London Series B — Biological Sciences 285, 20180975.

Interest in the evolutionary origins and drivers of warfare in ancient and contemporary small-scale human societies has greatly increased in the last decade, and has been particularly spurred by exciting archaeological discoveries that suggest our ancestors led more violent lives than previously documented. However, the striking observation that warfare is an almost-exclusively male activity remains unexplained. Three general hypotheses have been proposed, concerning greater male effectiveness in warfare, lower male costs, and patrilocality. But while each of these factors might explain why warfare is more common in men, they do not convincingly explain why women almost never participate. Here, we develop a mathematical model to formally assess these hypotheses. Surprisingly, we find that exclusively male warfare may evolve even in the absence of any such sex differences, though sex biases in these parameters can make this evolutionary outcome more likely. The qualitative observation that participation in warfare is almost exclusive to one sex is ultimately explained by the fundamentally sex-specific nature of Darwinian competition—in fitness terms, men compete with men and women with women. These results reveal a potentially key role for ancestral conditions in shaping our species’ patterns of sexual division of labour and violence-related adaptations and behavioural disorders.

Hitchcock TJ & Gardner A (2019) Parent-of-origin specific gene expression and dispersal. Current Opinion in Behavioral Sciences 25, 36-43.

Genes can behave in ways that are conditional upon their parent-of-origin. The best understood form of this is genomic imprinting (GI), which typically involves the silencing of a gene originating from one parent and the expression of its homologue originating from the other parent. A number of hypotheses have been proposed to explain GI, which may be grouped into those based on asymmetries of genetic interest versus those based on asymmetries of genetic information. Dispersal patterns can drive both of these asymmetries and modulate the costs and benefits of imprinting. GI may also have consequences for dispersal of individuals and genes, by driving imprinting of loci underpinning dispersal, altering the fitness consequences of dispersal, and affecting rates of introgression.

González-Forero M & Gardner A (2018) Inference of ecological and social drivers of human brain-size evolution. Nature 557, 554-557.

The human brain is unusually large. It has tripled in size from Australopithecines to modern humans and has become almost six times larger than expected for a placental mammal of human size. Brains incur high metabolic costs and accordingly a long-standing question is why the large human brain has evolved. The leading hypotheses propose benefits of improved cognition for overcoming ecological, social or cultural challenges. However, these hypotheses are typically assessed using correlative analyses, and establishing causes for brain-size evolution remains difficult. Here we introduce a metabolic approach that enables causal assessment of social hypotheses for brain-size evolution. Our approach yields quantitative predictions for brain and body size from formalized social hypotheses given empirical estimates of the metabolic costs of the brain. Our model predicts the evolution of adult Homo sapiens-sized brains and bodies when individuals face a combination of 60% ecological, 30% cooperative and 10% between-group competitive challenges, and suggests that between-individual competition has been unimportant for driving human brain-size evolution. Moreover, our model indicates that brain expansion in Homo was driven by ecological rather than social challenges, and was perhaps strongly promoted by culture. Our metabolic approach thus enables causal assessments that refine, refute and unify hypotheses of brain-size evolution.

Davies NG & Gardner A (2018) Monogamy promotes altruistic sterility in insect societies. Royal Society Open Science 55, 172190.

Monogamy is associated with sibling-directed altruism in multiple animal taxa, including insects, birds and mammals. Inclusive-fitness theory readily explains this pattern by identifying high relatedness as a promoter of altruism. In keeping with this prediction, monogamy should promote the evolution of voluntary sterility in insect societies if sterile workers make for better helpers. However, a recent mathematical population-genetics analysis failed to identify a consistent effect of monogamy on voluntary worker sterility. Here, we revisit that analysis. First, we relax genetic assumptions, considering not only alleles of extreme effect—encoding either no sterility or complete sterility—but also alleles with intermediate effects on worker sterility. Second, we broaden the stability analysis—which focused on the invasibility of populations where either all workers are fully sterile or all workers are fully reproductive—to identify where intermediate pure or mixed evolutionarily stable states may occur. Third, we consider a broader range of demographically explicit ecological scenarios relevant to altruistic worker non-reproduction and to the evolution of eusociality more generally. We find that, in the absence of genetic constraints, monogamy always promotes altruistic worker sterility and may inhibit spiteful worker sterility. Our extended analysis demonstrates that an exact population-genetics approach strongly supports the prediction of inclusive-fitness theory that monogamy promotes sib-directed altruism in social insects.

Faria GS, Varela SAM & Gardner A (2018) The relation between R. A. Fisher’s sexy-son hypothesis and W. D. Hamilton’s greenbeard effect. Evolution Letters. doi:10.1002/ev13.53

Recent years have seen a growing interest in the overlap between the theories of kin selection and sexual selection. One potential overlap is with regards to whether R. A. Fisher’s “sexy-son” hypothesis, concerning the evolution of extravagant sexual ornamentation, may be framed in terms of W. D. Hamilton’s greenbeard effect, concerning scenarios in which individuals carry an allele that allows them to recognize and behave differently toward other carriers of the same allele. Specifically, both scenarios involve individuals behaving differently toward social partners who exhibit a phenotypic marker, with linkage disequilibrium between marker and behavior loci ensuring genetic relatedness between actor and recipient at the behavior locus. However, the formal connections between the two theories remain unclear. Here, we develop these connections by: (1) asking what kind of greenbeard is involved in the sexy-son hypothesis; (2) exploring the relationship between the problem of “falsebeards” and the “lek paradox”; (3) investigating whether these two problems may be resolved in analogous ways; and (4) determining whether population structure facilitates both of these evolutionary phenomena. By building this conceptual bridge, we are able to import results from the field of kin selection to sexual selection, and vice versa, yielding new insights into both topics.