Sexual selection theory predicts a trade-off between premating (ornaments and armaments) and postmating (testes and ejaculates) sexual traits, assuming that growing and maintaining these traits is costly and that total reproductive investments are limited. The number of males in competition, the reproductive gains from investing in premating sexual traits, and the level of sperm competition are all predicted to influence how males allocate their finite resources to these traits. Yet, empirical examination of these predictions is currently scarce. Here, we studied relative expenditure on pre- and postmating sexual traits among frog species varying in their population density, operational sex ratio and the number of competing males for each c...
Background: Reproductive skew, the uneven distribution of reproductive success among individuals, is...
Our knowledge about genetic mating systems and the underlying causes for and consequences of variati...
Sex differences in parental care are thought to arise from differential selection on the sexes. Sexu...
Sexual selection theory predicts a trade-off between premating (ornaments and armaments) and postmat...
Sexual selection theory predicts a trade-off between premating (ornaments and armaments) and postmat...
Sperm competition theory assumes a trade-off between precopulatory traits that increase mating succe...
Trade-offs between pre- and postcopulatory traits influence their evolution, and male expenditure on...
Frog reproductive modes are complex phenotypes that include egg/clutch characteristics, oviposition ...
Sexual size dimorphism (SSD) varies in animals from male biased to female biased. The evolution of S...
Sexual size dimorphism (SSD) is one of the most common ways in which males and females differ. Male-...
The evolution of sperm quality and quantity is shaped by various selective processes, with sperm com...
Background: Recent comparative studies of several taxa have found that within-species variation in s...
Rensch's rule suggests that sexual size dimorphism (SSD) increases with species size when males are ...
Little is known about the operation of male mate choice in systems with perceived high costs to male...
Background: Reproductive skew, the uneven distribution of reproductive success among individuals, is...
Our knowledge about genetic mating systems and the underlying causes for and consequences of variati...
Sex differences in parental care are thought to arise from differential selection on the sexes. Sexu...
Sexual selection theory predicts a trade-off between premating (ornaments and armaments) and postmat...
Sexual selection theory predicts a trade-off between premating (ornaments and armaments) and postmat...
Sperm competition theory assumes a trade-off between precopulatory traits that increase mating succe...
Trade-offs between pre- and postcopulatory traits influence their evolution, and male expenditure on...
Frog reproductive modes are complex phenotypes that include egg/clutch characteristics, oviposition ...
Sexual size dimorphism (SSD) varies in animals from male biased to female biased. The evolution of S...
Sexual size dimorphism (SSD) is one of the most common ways in which males and females differ. Male-...
The evolution of sperm quality and quantity is shaped by various selective processes, with sperm com...
Background: Recent comparative studies of several taxa have found that within-species variation in s...
Rensch's rule suggests that sexual size dimorphism (SSD) increases with species size when males are ...
Little is known about the operation of male mate choice in systems with perceived high costs to male...
Background: Reproductive skew, the uneven distribution of reproductive success among individuals, is...
Our knowledge about genetic mating systems and the underlying causes for and consequences of variati...
Sex differences in parental care are thought to arise from differential selection on the sexes. Sexu...