Sex differences in lifespan are ubiquitous, but the underlying causal factors remain poorly understood. Inter- and intrasexual social interactions are well known to influence lifespan in many taxa, but it has proved challenging to separate the role of sex-specific behaviours from wider physiological differences between the sexes. To address this problem, we genetically manipulated the sexual identity of the nervous system—and hence sexual behaviour—in Drosophila melanogaster, and measured lifespan under varying social conditions. Consistent with previous studies, masculinization of the nervous system in females induced male-specific courtship behaviour and aggression, while nervous system feminization in males induced male–male courtship an...
Sex differences in ageing and lifespan are ubiquitous in nature. The "unguarded-X” hypothesis (UXh) ...
A number of studies have documented the evolution of female resistance to mate harm in response to t...
Males and females often maximize fitness by pursuing different reproductive strategies, with males c...
Sex differences in lifespan are ubiquitous, but the underlying causal factors remain poorly understo...
Sex differences in lifespan are ubiquitous, but the underlying causal factors remain poorly understo...
Sex differences in lifespan are ubiquitous, but the underlying causal factors remain poorly understo...
Sex differences in lifespan are ubiquitous, but the underlying causal factors remain poorly understo...
Sex differences in lifespan are ubiquitous, but the underlying causal factors remain poorly understo...
Sex differences in lifespan are ubiquitous, but the underlying causal factors remain poorly understo...
Sex differences in lifespan are ubiquitous, but the underlying causal factors remain poorly understo...
Sex differences in lifespan are ubiquitous, but the underlying causal factors remain poorly understo...
Sexual dimorphism for lifespan (SDL) is widespread, but poorly understood. A leading hypothesis, whi...
Sex differences in ageing rates and lifespan are common in nature, and an enduring puzzle for evolut...
Abstract: Sexual dimorphism in somatic investment may be shaped by two distinct forms of sexual conf...
Sex differences in ageing and lifespan are ubiquitous in nature. The "unguarded-X” hypothesis (UXh) ...
A number of studies have documented the evolution of female resistance to mate harm in response to t...
Males and females often maximize fitness by pursuing different reproductive strategies, with males c...
Sex differences in lifespan are ubiquitous, but the underlying causal factors remain poorly understo...
Sex differences in lifespan are ubiquitous, but the underlying causal factors remain poorly understo...
Sex differences in lifespan are ubiquitous, but the underlying causal factors remain poorly understo...
Sex differences in lifespan are ubiquitous, but the underlying causal factors remain poorly understo...
Sex differences in lifespan are ubiquitous, but the underlying causal factors remain poorly understo...
Sex differences in lifespan are ubiquitous, but the underlying causal factors remain poorly understo...
Sex differences in lifespan are ubiquitous, but the underlying causal factors remain poorly understo...
Sex differences in lifespan are ubiquitous, but the underlying causal factors remain poorly understo...
Sexual dimorphism for lifespan (SDL) is widespread, but poorly understood. A leading hypothesis, whi...
Sex differences in ageing rates and lifespan are common in nature, and an enduring puzzle for evolut...
Abstract: Sexual dimorphism in somatic investment may be shaped by two distinct forms of sexual conf...
Sex differences in ageing and lifespan are ubiquitous in nature. The "unguarded-X” hypothesis (UXh) ...
A number of studies have documented the evolution of female resistance to mate harm in response to t...
Males and females often maximize fitness by pursuing different reproductive strategies, with males c...