Correlational evidence of a sexually-selected handicap

Handicap models of sexual selection predict that ornaments must be costly to produce and/or to wear and maintain; only then can they evolve as reliable signals of genetic quality. We investigated in the laboratory one potential cost of possessing ornaments, using the viviparous fish Girardinichthys multiradiatus and its natural predator, the snake Thamnophis melanogaster. We found that female G. multiradiatus show preferences for males with larger fins, as measured from body correlates. Males with a morphology attractive to females, however, were more likely to be captured by snakes than were other males (Fig. 5). Greater vulnerability to snakes cannot be explained as a result of snake visual preferences, because snakes responded similarly to males and females (Fig. 6). Finally, males, particularly dominant ones, were more likely to inspect foraging snakes than were females (Fig. 7). We conclude that male Girardinichthys multiradiatus experience a sexually-selected handicap due to reduced mobility resulting from having enlarged fins.     

Search costs influence the spatial distribution,but not the level,of extra-pair mating in tree swallows

Costs of searching for a mate are an important component of models of sexual selection, yet they have rarely been examined in wild populations of vertebrates. In this paper, we report an experiment in which we handicapped female tree swallows by clipping some flight feathers. This manipulation increased the costs of flight and searching for extra-pair mates. Despite these costs, handicapped females had the same level of extra-pair mating (percentage of extra-pair young, percentage of broods with extra-pair young, and the number of extra-pair sires per brood) as control females. However, handicapped females were more likely to have young sired by extra-pair males that lived closer to her nest than control females. This change in the distribution of extra-pair mating was most likely due to female choice rather than male coercion, and it suggests that extra-pair mating has significant benefits to females. One important implication of our study is that ecological and social factors that influence search costs could affect the spatial distribution of extra-pair sires and, consequently, the intensity of sexual selection. These effects may have been overlooked in previous studies that did not identify extra-pair sires.     

Ornamentation predicts reproductive success in female pipefish

In the sex-role reversed pipefish Syngnathus typhle females compete for access to males and males are choosy. Females develop a temporary ornament when competing over mates with other females and when performing nuptial dances with males. This ornament is an amplification of the normal striped pattern in these fishes. We here show experimentally that (1) the contrast of this normal pattern forecasts the extent to which the ornament is shown, (2) contrast and ornamentation honestly signal female quality (egg numbers), (3) contrast and ornamentation accurately predict female mating success, (4) contrast is a phenotypically plastic trait specifically exaggerated under situations of female – female competition, and (5) neither contrast nor ornament are energetically expensive to the females (i.e., they are independent of short-term nutritional status). Hence, as predicted in sex-role reversed species, ornament design is constrained by costs to female fecundity: an energetically demanding ornament would impair on a female's ability to produce eggs. The type of ornament described here is the expected one, costly for reasons other than being energetically expensive to produce. Received: 4 April 1996 / Accepted after revision: 27 October 1996     

Racketed tail of the male and female turquoise-browed motmot: male but not female tail length correlates with pairing success,performance, and reproductive success

Both males and females of many avian species maintain elaborate plumage traits, and elaborate monomorphic plumage may convey adaptive benefits to one or both sexes as inter- or intraspecific signals. Both sexes of the turquoise-browed motmot (Eumomota superciliosa) are elaborately plumed with long racket-tipped tail. I investigated whether the racketed tail functions as a sexually selected signal in one or both sexes by testing the predictions that males and/or females with the largest tails have: (1) greater pairing success, (2) greater reproductive performance (clutch-initiation date, clutch size, and hatching success), and (3) greater reproductive success. Yearling males with longer denuded rachises (wires) on the central tail feathers had greater pairing success. In addition, adult males with longer wires paired with females who laid larger clutches, had greater hatching success independent of clutch size, and fledged more young. There was no relationship between female tail plumage and pairing success, reproductive performance, or fledgling success. These results are consistent with the hypothesis that male tail plumage functions as a mate choice or status signal, but that the tail of the female does not function in a sexually selected context. I discuss alternative hypotheses for the evolutionary maintenance of the elaborate female tail plumage.     

No evidence for female mate choice based on genetic similarity in the túngara frog Physalaemus pustulosus

In most sexually reproducing animals, the behavior of one or both sexes during courtship critically influences the success at mating of the opposite sex. This behavior is often interpreted as “mate choice,” and there is great interest in why such choices are exercised. The explanation for the evolution of mate choice that has received the most attention and generated the most controversy is based on assumed genetic effects. In this study, we investigated whether female túngara frogs, which choose mates based on acoustic cues, have a preference for genetically less related males. Specifically, we determine if there is disassortive mating based on microsatellite markers, if there is information in the advertisement call that could be used to assess genetic similarity, and if females exhibit acoustic-based mating preferences that would promote choice for genetic diversity. Using seven microsatellite markers, we found no correlation of male call similarity and male genetic relatedness. Female choice experiments showed no female preference for calls of less related males, and there was no evidence for inbreeding avoidance in the field. Our results do not support the hypothesis of mate choice based on information about genetic relatedness conveyed by acoustic signals in túngara frogs.     

Family insurance: kin selection and cooperative breeding in a solitary primate (Microcebus murinus)

Lactation imposes substantial physiological costs on mothers and should therefore not be directed towards foreign offspring. Such allonursing, however, is common in mammal species that share roosts. Hypotheses to explain allonursing among such plural breeders include misdirected parental care, milk evacuation, brood parasitism, reciprocity, and kin selection. The necessary behavioral data, in combination with data on kinship and kin recognition, have rarely been available to distinguish among these explanations, however. In this study, we provide evidence for cooperative nursing and adoption by plural-breeding females in a nocturnal primate, the gray mouse lemur (Microcebus murinus), in which females forage solitarily during the night, but form day-time sleeping groups with one to two other females. We observed 34 resident females in an 8 ha study area in Kirindy Forest, Madagascar, over three consecutive annual breeding seasons and determined genetic relationships among all members of this population. Five sleeping groups of adult females were filmed inside their roosts during one breeding season after females gave birth. The composition of groups changed substantially across years, but they always consisted of close maternal relatives. All females within a group gave birth to one to three infants. They regularly transferred only their own offspring among roosting sites, demonstrating an ability to discriminate between their own and other’s offspring, but they regularly groomed and nursed related offspring other than their own and adopted related dependent young after their mother’s death. Kin selection may therefore be the main selective force behind cooperative breeding among these closely related females with a high mortality risk, providing each of them with family insurance.     

Sexual selection in darkness? Female mating preferences in surface- and cave-dwelling Atlantic mollies,<Emphasis Type="Italic"> Poecilia mexicana</Emphasis> (Poeciliidae,Teleostei)

In many species, females prefer large males as mating partners. Male size can easily be determined visually. We examined how such mate choice evolves when individuals are deprived of sensory information previously used to determine male quality. Using a cave-dwelling population of Atlantic mollies, Poecilia mexicana, as a model, we asked whether the female mating preference for large male body size still occurs in this cave fish, or whether it is lacking due to the absence of visual communication in the cave environment. In simultaneous choice tests we compared the time females spent with a large or a small male. In the river-dwelling and cave-dwelling fish, as well as the population originating from the cave entrance, we found a significant preference for large males in light. Hence, the ancestral mating preference of surface-dwelling mollies has been maintained during the evolution of the cave form. However, only the cave population exhibited a mating preference in darkness. Determination of male body size appears to have been taken over by a non-visual sensory system, probably the lateral line.Communicated by K. Lindström     

A quantitative methodology for indexing environmental sensitivity and pollution potential

A methodology for rating the suitability of sites forthe location of industrial facilities is formulated and appliedto the case of a coal-fired power plant location. The methodologycomprises two major interlinked components: the environmentalplant location indexing component, which involves theidentification, scaling and weighting of environmentalsensitivity factors; and the impact analysis component, whichinvolves the superimposition of the pollution generation impactsof an industrial facility on spatially gridded zones of variousenvironmental sensitivities. For each rectangular areal unitdefined by a square grid, the Unit Pollution Potential Index isdetermined by the severity and distribution of key environmentalsensitivity factors and the coverage of superimposed pollutanteffects as determined by contaminant fate and transport models.For any alternative site of a planned facility, the summation ofthe unit indices over the area of influence of the facilityprovides the quantitative Pollution Index, which can be used as abasis for comparison of alternative sites for planned facilities.For this paper, this methodology is applied to the hypotheticalcase of the siting of a coal-fired power plant in thenortheastern region of the United States, in which threealternative sites are considered. The three sites: A, B and Cyielded indices of 47.83, 47.91 and 47.6, respectively, indicatingthat site C is the most suitable for siting the power plant.     

A Scenario Optimization Model for Dynamic Reserve Site Selection

Conservation planners are called upon to make choices and trade-offs about the preservation of natural areas for the protection of species in the face of development pressures. We addressed the problem of selecting sites for protection over time with the objective of maximizing species representation, with uncertainty about future site development, and with periodic constraints on the number of sites that can be selected. We developed a 0–1, linear optimization model with 2 periods to select the sites that maximize expected species coverage subject to budget constraints. The model is based on the idea that development uncertainty can be characterized by a set of scenarios, each of which is a possible second-period development outcome for the set of sites. We also suggest that our 2-period model can be used in a sequential fashion that is consistent with adaptive planning. Results are presented for the Fox River watershed in Chicago.     

Representational success: A new paradigm for achieving species protection by reserve site selection

Models for designing habitat reserve networks have focused on minimizing the number of sites necessary to cover each species one or more times. A solution to this problem is usually one from among a large number of alternative optimal configurations of sites. This paper develops an iterative method for building reserve networks that produces an optimal solution to the species set covering problem (SSCP) and also maximizes the number of species covered two or more times, three or more times, and so on, conditional on the solution to the previous iteration. We refer to this as representational success. Thus, a pareto optimal species set covering is achieved that is preferable to an arbitrary optimal solution to the SSCP.