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PubMed2000

Incipient speciation in sympatric Nicaraguan crater lake cichlid fishes: sexual selection versus ecological diversification.

The growing body of empirical evidence for sympatric speciation has been complemented by recent theoretical treatments that have identified evolutionary conditions conducive to speciation in sympatry. The Neotropical Midas cichlid (Amphilophus citrinellum) fits both of the key characteristics of these models, with strong assortative mating on the basis of a colour polymorphism coupled with trophic and ecological differentiation derived from a polymorphism in their pharyngeal jaws. We used microsatellite markers and a 480 bp fragment of the mitochondrial DNA control region to study four polymorphic populations of the Midas cichlid from three crater lakes and one large lake in Nicaragua in an investigation of incipient sympatric speciation. All populations were strongly genetically differentiated on the basis of geography. We identified strong genetic separation based on colour polymorphism for populations from Lake Nicaragua and one crater lake (Lake Apoyo), but failed to find significant genetic structuring based on trophic differences and ecological niche separation in any of the four populations studied. These data support the idea that sexual selection through assortative mating contributes more strongly or earlier during speciation in sympatry than ecological separation in these cichlids. The long-term persistence of divergent cichlid ecotypes (as measured by the percentage sequence divergence between populations) in Central American crater lakes, despite a lack of fixed genetic differentiation, differs strikingly from the patterns of extremely rapid speciation in the cichlids in Africa, including its crater lakes. It is unclear whether extrinsic environmental factors or intrinsic biological differences, e.g. in the degree of phenotypic plasticity, promote different mechanisms and thereby rates of speciation of cichlid fishes from the Old and New Worlds.

Animals↗
PubMed1981

Sexual selection in Drosophila silvestris of Hawaii.

Previous discovery that Drosophila melanogaster females tend to discriminate in mating against phenotypes of earliest courting males prompted a study of the Hawaiian species D. silvestris. Tibial bristle variation in males from opposite coasts of the island of Hawaii functions in courtship, and the possibility that females can distinguish males differing in the tibial trait is explored. Mating tests, designed to give each female and male an alternative choice between two individuals of opposite sex every 30 min, consisted of intrapopulation tests with a strain derived from an eastern (Kilauea) population and interpopulation tests between that strain and one derived from a western (Kahuku) population. Males were given initial combat tests, with "winners" then used in mating (except one test with "loser" males). Matings (52-55%) were classified into categories according to the readiness of the female to mate and sequence of courtship. Low-threshold females (accepting the first male after less than four courtship bouts) occurred at 30-35%. Among intrapopulational tests, females (with higher threshold) accepted first- and second-courting males about equally (25:36, respectively), but for male success in mating, the winning of initial intermale combats and the uniformity of courtship effort tended to be important criteria. Among interpopulation tests, homogamic matings were nearly equal (25% each), but heterogamic matings contrasted in that Kilauea females were reluctant to mate with Kahuku males (14%), while reciprocal matings occurred most frequently (34%). Females favored males second to court, particularly when a Kilauea male (with extra tibial bristles) was the second male. Thus a morphological feature likely to be influential in mating is demonstrated to be so; and sexual selection is operating via male-male combat plus discrimination in favor of particular opposite-sex individuals in this species.

Journal Article↗
PubMed1983

Reproductive suppression among female mammals: implications for biomedicine and sexual selection theory.

Female mammals experience a very high and often unappreciated rate of reproductive failure. Among human pregnancies alone, over 50 per cent fail between conception and parturition, and the majority of these failures are unexplained. These findings present important problems for evolutionary theory as well as for health care practices. This paper addresses these high rates of reproductive failure among mammals, by extending the work of a number of evolutionary biologists regarding the reproductive consequences of environmental adversity. The basic model upon which we elaborate, termed the Reproductive Suppression Model, argues that females can optimize their lifetime reproductive success by suppressing reproduction when future conditions for the survival of offspring are likely to be sufficiently better than present ones as to exceed the costs of the suppression itself. These costs are a function of reproductive time lost and the direct phenotypic effects of the suppression itself. To evaluate the benefits and costs of suppression, the following types of cues should be assessed: the female's physical and mental health, her stage of reproduction, the physical and genetic status of her offspring, and the external conditions at the time of birth. We also examine various issues of social suppression, whereby the conditions for survival of offspring are a function of the reproduction and support of other group members. Under such conditions, some females may be able to improve current conditions for reproduction by suppressing the reproduction of others. Field data from our own work are presented, describing socially mediated reproductive competition among continuously breeding female yellow baboons and among female hoary marmots. Social suppression in other mammals is also evaluated, including that in human beings, and we conclude with some implications of the Reproductive Suppression Model for sexual selection theory regarding female-female reproductive competition, as well as human health care.

Abortion, Spontaneous↗
PubMed1997

Sexual selection in Japanese macaques I: female mate choice or male sexual coercion?

Mate choice is defined as a behavioural pattern in one sex which increases the probability of fertile matings with certain members of the opposite sex. The chosen sex may use force, however, to coerce matings from reluctant members of the choosing sex. In a confined group of Japanese macaques, Macaca fuscata fuscatahoused at the Primate Research Institute of Kyoto University, Japan, behavioural and endocrine data were combined to assess the validity of several mate-choice behaviours and the potential influence of sexual coercion. Preliminary evidence was found for both female mate choice of males and male sexual coercion of females. Both female proximity maintenance towards males and male aggression towards females were correlated with an increase in fertile matings. Most male aggression appeared to be the by-product of increased time spent in proximity due to female proximity maintenance, but some male aggression appeared to be sexual coercion. These results are interpreted in light of recent research on male sexual coercion, and a tentative model of mate choice for this species is proposed.1997The Association for the Study of Animal Behaviour

Journal Article↗
PubMed2006

Good genes sexual selection in nature.

Whether the mate sampling and choice performed by females in nature influences offspring performance is a controversial issue in theory and an open empirical question. Pronghorn (Antilocapra americana) females engage in an obvious and energetically expensive mate sampling process to identify vigorous males. Although individual females sample independently, their choices converge on a small proportion of males that sire most young. Offspring of attractive males were more likely to survive to weaning and to age classes as late as 5 years, resulting in a selection differential, calculated by expected differences in lifetime number of offspring weaned, of 0.32 against random mating. Enhanced survival to weaning appeared to be accomplished by faster growth rates. Females compensated for matings with a less attractive mate by elevating rates of milk delivery to their young. Because pronghorn males do not have costly ornaments, we conclude that female choice for good genes can exist in the absence of ornaments. Furthermore, female choice may be important and unrecognized as a force that can lower population genetic load.

Animals↗
PubMed1989

Amplifiers and the handicap principle in sexual selection: a different emphasis.

Population genetic models have shown that female choice is a potential cause of the evolution of male display. In these models the display is assumed to be the immediate object of female choice. Here I present an explicit genetic model that shows that male display can evolve as a consequence of female choice even when the display is not the immediate object of choice. When females initially base their preferences on the existence of variance in a cue that is correlated with male viability, a rare display can evolve to fixation if it amplifies the previously recognized differences in males, (i.e. if it increases the resolution power of females with respect to the original cue). By definition, amplifying displays (or amplifiers) increase mating success of the more viable males and decrease mating success of the less viable males. Therefore, the higher the frequency of the preferred, more viable males, the more likely it is that amplifiers will evolve to fixation. The evolution of an amplifier is further facilitated by a genetic association that is built up between the amplifier allele and the more viable allele. If the expression of the amplifier is limited to the more viable males, the amplifier will evolve to fixation provided only that the change in total fitness to the more viable males (higher mating success, lower viability), is positive.

Alleles↗
PubMed2004

Female preference for multiple condition-dependent components of a sexually selected signal.

Theoretical models explain the evolution of multi-cue mate-choice decisions from a trade-off between benefits owing to improved assessment of potential mates and costs linked to the use of multiple signals. However, empirical support for these basic assumptions is lacking. In field crickets (Gryllus campestris) we experimentally investigated the female preference to variation in two key components of the male calling song: carrier frequency and chirp rate. Previous studies have revealed carrier frequency and chirp rate as reliable indicators of male quality that reflect past condition and current condition, respectively. In a two-way choice experiment, females significantly preferred test songs of lower carrier frequency and higher chirp rate, but prioritized the carrier frequency over the chirp rate. Hence, the static long-term indicator of mate quality was weighted more than the dynamic short-term one. Our results thus indicate that females integrate information from independent condition-dependent cues to discriminate between available males in mate-choice decisions.

Acoustic Stimulation↗
PubMed2000

Runaway sexual selection when female preferences are directly selected.

We introduce models for the runaway coevolution of female mating preferences and male display traits. The models generalize earlier results by allowing for direct natural selection on the preference, arbitrary forms of mate choice, and fairly general assumptions about the underlying genetics. Results show that a runaway is less likely when there is direct selection on the preference, but that it is still possible if there is a sufficiently large phenotypic correlation between the female's preference and the male's trait among mated pairs. Comparison of three preference functions introduced by Lande (1981) shows that open-ended preferences are particularly prone to a runaway, and that absolute preferences require very large differences between females in their preferences. We analyze the causes of the runaway seen in a model developed by Iwasa and Pomiankowski (1995).

Animals↗