Jutta M. Schneider
University of Hamburg
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Proceedings of the Royal Society of London. Series B, Biological Sciences | 2000
Mark A. Elgar; Jutta M. Schneider; Marie E. Herberstein
Sexual conflict theory predicts an antagonistic coevolution, with each sex evolving adaptations and counter–adaptations to overcome a temporary dominance of the other sex over the control of paternity. Polyandry allows sexual selection to operate after mating has commenced, with male and female interests competing for control of fertilization. There are numerous examples of male control of paternity, but few studies have unambiguously revealed female control. Attributing variance in paternity to females is often difficult since male and female influences cannot be separated unambiguously. However, we show that polyandrous female orb–web spiders Argiope keyserlingi (Araneidae) control the paternity of their offspring by adjusting the timing of sexual cannibalism. Our experiments reveal that females copulating with relatively smaller males delay sexual cannibalism, thereby prolonging the duration of copulation, and that these males consequently fertilize relatively more eggs.
Journal of Evolutionary Biology | 2000
Jutta M. Schneider; M. E. Herberstein; F. C. De Crespigny; Sharada Ramamurthy; Mark A. Elgar
Sexual selection, through female choice and/or male–male competition, has influenced the nature and direction of sexual size dimorphism in numerous species. However, few studies have examined the influence of sperm competition on size dimorphism. The orb‐web spider Nephila edulis has a polygamous mating system and extreme size dimorphism. Additionally, the frequency distribution of male body size is extremely skewed with most males being small and few large. The duration of copulation, male size and sexual cannibalism have been identified as the significant factors determining patterns of sperm precedence in spiders. In double mating trials, females were assigned to three treatments: either they mated once with both males or the first or the second male was allowed to mate twice. Paternity was strongly associated with the duration of copulation, independent of mating order. Males that were allowed to mate twice not only doubled the duration of copulation but also their paternity. Small males had a clear mating advantage, they copulated longer than large males and fertilized more eggs. Males of different sizes used different tactics to mate. Large males were more likely to mate through a hole they cut into the web, whereas small males approached the female directly. Furthermore, small males usually mated at their first attempt but large males required several attempts before mating took place. There was no obvious female reaction towards males of different sizes.
Evolution | 2005
Lutz Fromhage; Mark A. Elgar; Jutta M. Schneider
Abstract The traditional paradigm of male polygamy and female monogamy has been replaced by the recognition that both sexes may typically mate with several partners. As a consequence, much attention has focused on the evolution of polyandry, while the evolutionary significance of monogyny (male monogamy) remains poorly understood. Monogyny, a taxonomically widespread mating system that includes dramatic examples of male self‐sacrifice, is predicted when the benefits of paternal investment exceed those of searching for additional mates. However, monogyny also occurs in animals lacking paternal investment, instead representing a form of paternity protection. It has been suggested that such mating systems are expected where the costs of mate search for males are high. However, this argument fails to recognize that if there is a low probability of a male finding a mate, then there may be a high probability that he will not need to defend his paternity. Using a mathematical model, we show that monogyny as a means of increasing paternity is favored when the sex ratio is male biased, but not necessarily by high search costs. The importance of a male‐biased sex ratio for the evolution of monogyny is supported by various empirical studies.
Oikos | 1998
Jutta M. Schneider; Yael Lubin
Reproductive strategies of males and females usually differ and, as a consequence, may impose asymmetric costs of reproduction on the two sexes and result in conflict between the sexes. In spiders, males do not provide parental care and females can store sufficient sperm for several clutches. These characteristics define the stage for a conflict between males and females that occurs mainly over the frequency of mating. Factors such as sexual size dimorphism, operational sex ratio, mating system and life-history strategies are likely to influence the degree of conflict and its outcome for different species. Male spiders may suffer large costs of mating due to mate search, assessment of female condition, courtship and cannibalistic tendencies of their mates. Courtship may reduce cannibalism, although in some cases, males benefit from being cannibalised by having an increased fertilisation rate or greater offspring fitness. In some species, limited mating capacities will increase the value of the current mating relative to future reproduction. Apart from a possible benefit of genetic variability within a clutch, females may not benefit from multiple mating and multiple mating may even be costly. Exceptions occur if additional resources are provided by males or when offspring fitness increases with additional mating. Forced copulation, prey theft, loss of the web and reduction of foraging time can all result in reduced reproductive success for females. We discuss the interacting influences of life-history traits (especially patterns of growth and maturation and sexual size dimorphism) and the reproductive strategies of males and females, using a semelparous spider, Stegodyphus lineatus (Eresidae), as an example of a species in which males and females can have strongly conflicting interests.
Genetica | 2010
Gabriele Uhl; Æ Stefan H. Nessler; Jutta M. Schneider
Low female mating frequencies often appear to be cases of direct male induction that can oppose female interests. Mating plugs are most obvious means leading to low degrees of multiple mating in females. In spiders, mating plugs are formed by a variety of amorphous materials, by the breakage of the male sperm transferring organ, or by the whole male that functions as a mating barrier. Our compilation of the available information on the presence of the various types of mating plugs suggests that plugs predominantly occur in entelegyne spiders. In this group, plugs do not interfere with oviposition since separate openings for insemination and oviposition are present. In contrast, mating plugs seem to be rare in haplogyne spiders that do not possess separate openings. The available experimental studies on the function of the different types of plugs suggest that plugs can be considered as male adaptations to avoid sperm competition. However, females in some cases were shown to have evolved means to prevent or control male manipulation or may selectively favour plug production in specific males, an aspect which has largely been neglected. In order to understand plug evolution and function we need to explore the morphological, behavioural and biochemical aspects involved and extend our approach to interactions between the sexes.
Advances in The Study of Behavior | 2004
Mark A. Elgar; Jutta M. Schneider
Publisher Summary “Sexual cannibalism” refers to females killing and consuming their male partner at some stage during courtship and mating. Sexual cannibalism can occur before or during mating, which will determine potential explanations for its occurrence. This chapter discusses sexual cannibalism in the context of both sexual and natural selection. The natural history and taxonomic distribution of sexual cannibalism is discussed. Various explanations of sexual cannibalism are outlined, emphasizing how the timing of sexual cannibalism changes the costs and benefits to males and females. The evolutionary significance of sexual cannibalism depends on whether it occurs before or after insemination. Preinsemination sexual cannibalism is a nonadaptive consequence of selection on aggressive foraging in juvenile females. It is an adaptive component of female foraging, where females trade off foraging and mating requirements. It is a radical form of female mate choice. Sexual cannibalism could have evolved through the process of sexual, rather than, natural selection. It is evident that sexual cannibalism facilitates both female choice and cryptic female choice. Female foraging strategies that include sexual cannibalism are strongly opposed by counter selection on male mating success.
Behavioral Ecology and Sociobiology | 2002
M. E. Herberstein; Jutta M. Schneider; Mark A. Elgar
Abstract. The costs of courtship and mating may include increased risks of predation, the transmission of pathogens, and a loss of foraging opportunities. Thus, a females decision to tolerate a courting male will depend upon how these costs offset the benefits of mating, which will depend on her reproductive and nutritional status. While these costs may be similar for mated and unmated females, the benefits of mating will be less for mated than virgin females. However, the cost of lost foraging opportunities may be higher for females with fewer nutritional reserves necessary for forming eggs. We examined how these costs and benefits influence the courtship and mating behaviour of male and female orb-web spiders, Argiope keyserlingi. In the field, females on webs that also contained a courting male intercepted fewer prey items per hour than females on webs without a male. In the laboratory, the presence of a courting male at the hub also attracted mantid predators to the web, increasing the risk of predation for both male and female. Staged mating experiments in the laboratory revealed that the frequency of female attacks and pre-copulatory cannibalism was greater among mated than virgin females. Feeding history did not affect aggression in virgin females but, among mated females, food-deprived spiders attacked and cannibalized males more frequently than sated females and only the latter ever remated. These differences in female behaviour influenced male mating strategies. Choice experiments demonstrated that males preferred to venture onto the silk threads of virgin rather than those of mated females. Similar patterns of mate selectivity were observed in the field; females with narrow abdomens attracted more males to the webs than females with broad abdomens, and copulations were observed more frequently among females with narrow abdomens. These smaller females are likely to be virgins that have recently molted. Males that preferentially mate with virgin females will not only avoid potentially fatal attacks but also obtain, on average, a higher fertilization success.
Evolution | 2005
Trine Bilde; Yael Lubin; Deborah R. Smith; Jutta M. Schneider; Alexei A. Maklakov
Abstract The social spiders are unusual among cooperatively breeding animals in being highly inbred. In contrast, most other social organisms are outbred owing to inbreeding avoidance mechanisms. The social spiders appear to originate from solitary subsocial ancestors, implying a transition from outbreeding to inbreeding mating systems. Such a transition may be constrained by inbreeding avoidance tactics or fitness loss due to inbreeding depression. We examined whether the mating system of a subsocial spider, in a genus with three social congeners, is likely to facilitate or hinder the transition to inbreeding social systems. Populations of subsocial Stegodyphus lineatus are substructured and spiders occur in patches, which may consist of kin groups. We investigated whether male mating dispersal prevents matings within kin groups in natural populations. Approximately half of the marked males that were recovered made short moves (< 5m) and mated within their natal patch. This potential for inbreeding was counterbalanced by a relatively high proportion of immigrant males. In mating experiments, we tested whether inbreeding actually results in lower offspring fitness. Two levels of inbreeding were tested: full sibling versus non-sib matings and matings of individuals within and between naturally occurring patches of spiders. Neither full siblings nor patch mates were discriminated against as mates. Sibling matings had no effect on direct fitness traits such as fecundity, hatching success, time to hatching and survival of the offspring, but negatively affected offspring growth rates and adult body size of both males and females. Neither direct nor indirect fitness measures differed significantly between within patch and between-patch pairs. We tested the relatedness between patch mates and nonpatch mates using DNA fingerprinting (TE-AFLP). Kinship explained 30% of the genetic variation among patches, confirming that patches are often composed of kin. Overall, we found limited male dispersal, lack of kin discrimination, and tolerance to low levels of inbreeding. These results suggest a history of inbreeding which may reduce the frequency of deleterious recessive alleles in the population and promote the evolution of inbreeding tolerance. It is likely that the lack of inbreeding avoidance in subsocial predecessors has facilitated the transition to regular inbreeding social systems.
Evolution | 2009
Matjaž Kuntner; Jonathan A. Coddington; Jutta M. Schneider
Genital morphology is informative phylogenetically and strongly selected sexually. We use a recent species-level phylogeny of nephilid spiders to synthesize phylogenetic patterns in nephilid genital evolution that document generalized conflict between male and female interests. Specifically, we test the intersexual coevolution hypothesis by defining gender-specific indices of genital complexity that summarize all relevant and phylogenetically informative traits. We then use independent contrasts to show that male and female genital complexity indices correlate significantly and positively across the phylogeny rather than among sympatric sister species, as predicted by reproductive character displacement. In effect, as females respond to selection for fecundity-driven fitness via giantism and polyandry (perhaps responding to male-biased effective sex ratios), male mechanisms evolve to monopolize females (male monogamy) via opportunistic mating, pre- and postcopulatory mate guarding, and/or plugging of female genitalia to exclude subsequent suitors. In males morphological symptoms of these phenomena range from self-mutilated genitalia to total castration. Although the results are compatible with both recently favored sexual selection hypotheses, sexually antagonistic coevolution, and cryptic female choice, the evidence of strong intersexual conflict and genitalic damage in both sexes is more easily explained as sexually antagonistic coevolution due to an evolutionary arms race.
Behavioral Ecology and Sociobiology | 2003
Lutz Fromhage; Gabriele Uhl; Jutta M. Schneider
The evolution of sexual cannibalism as the most extreme form of nuptial feeding is still poorly understood. Although increasing evidence suggests that female aggressiveness is related to other aspects of foraging behaviour, it is not clear whether the nutritional value of a male is sufficient to provide an adaptive significance for sexual cannibalism. A widely cited though rarely tested explanation is based on a paternal investment model, and predicts that consumption of a male results in increased female fecundity. The available evidence is either correlational or restricted to species with relatively large and potentially nutritious males, and different studies have come to different conclusions. Here we present a test of the paternal investment hypothesis using the very cannibalistic and highly size-dimorphic spider Argiope bruennichi. After a preset schedule, we had females consume none, one or two males independent of the females cannibalistic behaviour. Consumption of male bodies did not result in any detectable fitness benefit for the female: neither the number of clutches, nor clutch size or hatching success were affected by consumption of males. The frequency of cannibalism was around 80%, independent of the female mating status. We did not observe male complicity, but cannibalism was associated with prolonged copulation. This suggests a sexually selected benefit of cannibalism for males. We conclude that the paternal investment hypothesis does not explain the existence of sexual cannibalism in A. bruennichi and probably not in other spider species with a pronounced sexual size dimorphism.