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J A Endler

Publications and source records attributed to J A Endler.

9 recordsLinked to original sources
PubMed2001

Carotenoid scarcity, synthetic pteridine pigments and the evolution of sexual coloration in guppies (Poecilia reticulata).

Carotenoid-based sexual coloration is the classic example of an honest signal of mate quality. Animals cannot synthesize carotenoid pigments and ultimately depend on dietary sources. Thus, in carotenoid-poor environments, carotenoid coloration may be a direct indicator of foraging ability and an indirect indicator of health and vigour. Carotenoid coloration may also be affected, more directly, by parasites in some species. Carotenoids are not, however, the only conspicuous pigments available to animals. Pteridine pigments, with similar spectral properties, are displayed in the exoskeletons and wings of insects, the irides of birds and the skins of fishes, lizards and amphibians. Unlike carotenoids, pteridines are synthesized de novo by animals. We report that the orange spots that male guppies (Poecilia reticulata) display to females contain red pteridine pigments (drosopterins) in addition to carotenoids. We also examined the relationship between drosopterin production by males and carotenoid availability in the field. The results contrasted sharply with the hypothesis that males use drosopterins to compensate for carotenoid scarcity: males used more, not less, drosopterins in streams with higher carotenoid availability. The positive association between drosopterin use and carotenoid availability could reflect the costs of drosopterin synthesis or it could be a consequence of females preferring a particular pigment ratio or hue. Male guppies appear to use drosopterin pigments in a manner that dilutes, but does not eliminate, the indicator value of carotenoid coloration.

Animals↗
PubMed2001

Female guppies agree to differ: phenotypic and genetic variation in mate-choice behavior and the consequences for sexual selection.

Variation among females in mate choice may influence evolution by sexual selection. The genetic basis of this variation is of interest because the elaboration of mating preferences requires additive genetic variation in these traits. Here we measure the repeatability and heritability of two components of female choosiness (responsiveness and discrimination) and of female preference functions for the multiple ornaments borne by male guppies (Poecilia reticulata). We show that there is significant repeatable variation in both components of choosiness and in some preference functions but not in others. There appear to be several male ornaments that females find uniformly attractive and others for which females differ in preference. One consequence is that there is no universally attractive male phenotype. Only responsiveness shows significant additive genetic variation. Variation in responsiveness appears to mask variation in discrimination and some preference functions and may be the most biologically relevant source of phenotypic and genetic variation in mate-choice behavior. To test the potential evolutionary importance of the phenotypic variation in mate choice that we report, we estimated the opportunity for and the intensity of sexual selection under models of mate choice that excluded and that incorporated individual female variation. We then compared these estimates with estimates based on measured mating success. Incorporating individual variation in mate choice generally did not predict the outcome of sexual selection any better than models that ignored such variation.

Animals↗
PubMed2001

Direct and indirect sexual selection and quantitative genetics of male traits in guppies (Poecilia reticulata).

The ornamentation and displays on which sexual attractiveness and thus mating success are based may be complex and comprise several traits. Predicting the outcome of sexual selection on such complex phenotypes requires an understanding of both the direct operation of selection on each trait and the indirect consequences of selection operating directly on genetically correlated traits. Here we report the results of a quantitative genetic analysis of the ornamentation, sexual attractiveness, and mating success of male guppies (Poecilia reticulata). We analyze male ornamentation both from the point of view of single ornamental traits (e.g., the area of each color) and of composite measures of the way the entire pattern is likely to be perceived by females (e.g., the mean and contrast in chroma). We demonstrate that there is substantial additive genetic variation in almost all measures of male ornamentation and that much of this variation may be Y linked. Attractiveness and mating success are positively correlated at the phenotypic and genetic level. Orange area and chroma, the area of a male's tail, and the color contrast of his pattern overall are positively correlated with attractiveness and/or mating success at the phenotypic and genetic levels. Using attractiveness and mating success as measures of fitness, we estimate gradients of linear directional sexual selection operating on each male trait and use equations of multivariate evolutionary change to predict the response of male ornamentation to this sexual selection. From these analyses, we predict that indirect selection may have important effects on the evolution of male guppy color patterns.

Animals↗
PubMed1993

Some general comments on the evolution and design of animal communication systems.

Animal communication systems have evolved so that individuals can make decisions based upon the behaviour, physiology or morphology of others. Receiving mechanisms probably evolve to increase the efficiency and reliability of information reception whereas signals probably evolve to increase the efficiency of communication and reliability of manipulation of the receiving individual to the benefit of the emitter. The minimum requirement for clear reception suggests that any study of the evolution and design of communication systems must consider the factors that affect the quality of the received and processed signal. Critical information is needed about how the signal is generated and emitted, how it fares during transmission through air, water or substrate, how it is received and processed by the receiver's sensory and cognitive systems, and the factors which affect the fitness consequences of alternative ways of reacting to the information contained in the signal. These should allow predictions about the kinds and forms of signals used by animals signalling under known conditions. Phylogenetic history, and the geological time a clade spends in different signalling environments, will also affect signal evolution, and hence the success of predictions about signal design. We need to use methods of many different biological fields to understand the design and evolution of signals and signalling systems.

Animal Communication↗
PubMed1991

Variation in the appearance of guppy color patterns to guppies and their predators under different visual conditions.

Color patterns of natural populations of guppies (Poecilia reticulata) are a compromise between sexual selection and predation avoidance. Field data on ambient light spectra, water transmission spectra, courtship and attack distances, and cone pigments of guppies and their predators were used to calculate measures of conspicuousness of guppies under various combinations of visual conditions and vision. The results suggest that color patterns are relatively more conspicuous to guppies at the times and places of courtship and relatively less conspicuous at the times and places of maximum predator risk. Some implications to the evolution of vision, visual communication and behavior are discussed.

Animals↗
PubMed1988

Frequency-dependent predation, crypsis and aposematic coloration.

Frequency-dependent predation may maintain or prevent colour pattern polymorphisms in prey, and can be caused by a variety of biological phenomena, including perceptual processes (search images), optimal foraging and learning. Most species are preyed upon by more than one predator species, which are likely to differ in foraging styles, perceptual and learning abilities. Depending upon the interaction between predator vision, background and colour pattern parameters, certain morphs may be actively maintained in some conditions and not in others, even with the same predators. More than one kind of predator will also affect stability, and only slight changes in conditions can cause a transition between polymorphism and monomorphism. Frequency-dependent selection is not a panacea for the explanation of variation in animal colour patterns, although it may be important in some systems.

Animals↗
PubMed1987

Visual pigment polymorphism in the guppy Poecilia reticulata.

Visual pigment polymorphism similar to that found in primates is described in the photoreceptors of wild-caught guppies (Poecilia reticulata). Microspectrophotometric examination of retinal cells revealed rod visual pigments with a lambda max close to 503 nm. Classes of cones with lambda max around 410 and 465 nm were found, together with a population of pigments in the 529-579 nm range. It is in these long-wavelength cones that polymorphism occurs. Male guppies are highly polymorphic for body colour and it is possible that the cone polymorphism is related to the appreciation of the different yellow, orange and red carotenoid colour spots that are used in sexual display.

Animals↗
PubMed1973

Gene flow and population differentiation.

There are many possible spatial patterns of selection and gene flow that can produce a given cline structure; the actual geography of natural selection and gene flow must be worked out before an attempt is made to explain a given natural cline in terms of a model. The results of experimental and theoretical models show that it is possible for local differentiation to evolve parapatrically in spite of considerable gene flow if the selection gradients are relatively uniform. Irregularities in environmental gradients increase the sensitivity of clines to the effects of gene flow in proportion to the increase in the differences in gene frequencies between the emigrants and the demes receiving the immigrants. It is not necessary for a sharp spatial environmental change to be present for distinct differentiation to occur. In some cases even a gentle environmental gradient can give rise to marked spatial differentiation along a genetically continuous series of demes; such environmental differences may be below the practical limits of resolution in field studies. Any asymmetry in gene flow does not lead to dedifferentiation if the environmental gradient is smooth; it merely shifts the position of the transition zone between the differentiated areas from that which would be expected if there were no asymmetry. Abrupt geographic differences in gene, genotype, or morph frequencies should not, therefore, be interpreted as evidence for environmental changes in the immediate vicinity of the steepest part of the cline; neither should they be interpreted as evidence for geographic barriers, sharp environmental differences, or sexual isolation among the differentiated groups of populations when there are no other sources of evidence for these phenomena. Gene flow may be unimportant in the differentiation of populations along environmental gradients.

Animals↗