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Adaptive Explanations (adaptive + explanation)
Selected AbstractsFitness consequences of temperature-mediated egg size plasticity in a butterflyFUNCTIONAL ECOLOGY, Issue 6 2003K. Fischer Summary 1By randomly dividing adult females of the butterfly Bicyclus anynana, reared in a common environment, among high and low temperatures, it is demonstrated that oviposition temperature induces a plastic response in egg size. Females kept at a lower temperature laid significantly larger eggs than those ovipositing at a higher temperature. 2Cross-transferring the experimentally manipulated eggs between temperatures and investigating hatching success showed that a lower rearing temperature is more detrimental for the smaller eggs produced at a higher temperature than for the larger eggs produced at a lower temperature, supporting an adaptive explanation. 3However, when examining two potential mechanisms for an increased fitness of larger offspring (higher desiccation resistance of larger eggs and higher starvation resistance of larger hatchlings), no direct link between egg size and offspring fitness was found. Throughout, i.e. even under benign conditions, larger offspring had a higher fitness. 4Therefore, egg size should be viewed as a conveniently measurable proxy for the plastic responses induced by temperature, but caution is needed before implying that egg size per se is causal in influencing offspring traits. [source] Habitat specialization and adaptive phenotypic divergence of anuran populationsJOURNAL OF EVOLUTIONARY BIOLOGY, Issue 3 2005J. VAN BUSKIRK Abstract We tested for adaptive population structure in the frog Rana temporaria by rearing tadpoles from 23 populations in a common garden experiment, with and without larval dragonfly predators. The goal was to compare tadpole phenotypes with the habitats of their source ponds. The choice of traits and habitat variables was guided by prior information about phenotypic function. There were large differences among populations in life history, behaviour, morphological shape, and the predator-induced plasticities in most of these. Body size and behaviour were correlated with predation risk in the source pond, in agreement with adaptive population divergence. Tadpoles from large sunny ponds were morphologically distinct from those inhabiting small woodland ponds, although here an adaptive explanation was unclear. There was no evidence that plasticity evolves in populations exposed to more variable environments. Much among-population variation in phenotype and plasticity was not associated with habitat, perhaps reflecting rapid changes in wetland habitats. [source] Ecological diversification in a group of Indomalayan pitvipers (Trimeresurus): convergence in taxonomically important traits has implications for species identificationJOURNAL OF EVOLUTIONARY BIOLOGY, Issue 4 2004K. L. Sanders Abstract We analyse molecular and phenotypic evolution in a group of taxonomically problematic Indomalayan pitvipers, the Trimeresurus sumatranus group. Mitochondrial DNA sequencing provides a well-resolved phylogeny, with each species representing a distinct lineage. Multivariate morphological analysis reveals a high level of phenotypic differentiation, which is congruent between the sexes but does not reflect phylogenetic history. An adaptive explanation for the observed pattern of differentiation is supported by independent contrasts analysis, which shows significant correlations between current ecology and the characters that most account for the variation between taxa, including those that are presently used to identify the species. Reduced precipitation and altitude, and increased temperature, are correlated with higher numbers of scales on the head, body and tail. It is hypothesized that scale number plays an important role in heat and water exchange by influencing the area of exposed of interstitial skin, and that colour pattern variation reflects selection pressures involving camouflage and thermoregulation. Ecological convergence in traits used for classification is found to have important implications for species identification where taxa are distributed over varying environments. [source] Necks-for-sex or competing browsers?JOURNAL OF ZOOLOGY, Issue 1 2010A critique of ideas on the evolution of giraffe Abstract Recent years have witnessed a resurgence in tests of the evolution and origin of the great height and long neck of the giraffe Giraffa camelopardalis. The two main hypotheses are (1) long necks evolved through competition with other browsers allowing giraffe to feed above them (,competing browsers' hypothesis); or (2) the necks evolved for direct use in intra-sexual combat to gain access to oestrous females (,necks-for-sex' hypothesis). Here, we review recent developments and their relative contribution in explaining giraffe evolution. Trends from Zimbabwean giraffes show positive allometry for male necks and isometry for female necks relative to body mass, while comparative analyses of the cervical versus the total vertebral column of the giraffe, okapi and fossil giraffe suggest selection specifically on neck length rather than on overall height. Both support the necks-for-sex idea. Neither study, however, allows us to refute one of the two ideas. We suggest new approaches for quantifying the relative importance of the two hypotheses. A direct analysis of selection pressure on neck length via survival and reproduction should clarify the mechanism maintaining the trait, while we predict that short robust ossicones should have arisen concurrently with incipient neck elongation if sexual selection was the main selective driver. The main challenge for the competing browser hypothesis is to explain why giraffe have remained about 2 m taller than their tallest competitors for over 1 Myr, whereas the sexual selection hypothesis cannot provide an adaptive explanation for the long neck of female giraffe. We conclude that probably both mechanisms have contributed to the evolution and maintenance of the long neck, and their relative importance can be clarified further. [source] The evolution of alternative morphs: density-dependent determination of larval colour dimorphism in a butterflyBIOLOGICAL JOURNAL OF THE LINNEAN SOCIETY, Issue 2 2009KARL GOTTHARD Understanding the ultimate causes for the presence of polymorphisms within populations requires knowledge of how the expression of discrete morphs is regulated. In the present study, we explored the determination mechanism of a colour dimorphism in larvae of the butterfly Pararge xiphia (Satyrinae: Nymphalidae) with the ultimate aim of understanding its potential adaptive value. Last-instar larvae of P. xiphia develop into either a green or a brown morph, although all individuals are invariably green during the preceding three instars. A series of laboratory experiments reveal that morph development is strongly environmentally dependent and not the result of alternative alleles at one locus. Photoperiod, temperature, and in particular larval density, all influenced morph determination. The strong effect of a high larval density in inducing the brown morph parallels other known cases of density-dependent melanization in Lepidopteran larvae. Because melanization is often correlated with increased immune function, this type of determination mechanism is expected to be adaptive. However, the ecology and behaviour of P. xiphia larvae suggests that increased camouflage under high-density conditions may be an additional adaptive explanation. We conclude that the colour dimorphism of P. xiphia larvae is determined by a developmental threshold that is influenced both by heredity and by environmental conditions, and that selection for increased immune function and camouflage under high-density conditions may be responsible for maintaining the dimorphism. © 2009 The Linnean Society of London, Biological Journal of the Linnean Society, 2009, 98, 256,266. [source] The relationship between host selection behaviour and offspring fitness in a koinobiont parasitoidECOLOGICAL ENTOMOLOGY, Issue 4 2000Ana Rivero Summary 1. When host quality varies, optimal foraging theory assumes that parasitic wasps select hosts in a manner that increases their individual fitness. In koinobiont parasitoids, where the hosts continue developing for a certain period of time after parasitisation, host selection may not reflect current host quality but may be based on an assessment of future growth rates and resources available for the developing larvae. 2. When presented with hosts of uniform quality, the koinobiont parasitoid Leptomastix dactylopii exhibits a characteristic host-selection behaviour: some hosts are accepted for oviposition on first encounter, while others are rejected several times before an egg is laid in them, a behaviour that is commonly associated with a changing host acceptance threshold during the course of a foraging bout. 3. The fitness of the offspring that emerged from hosts accepted immediately upon encounter was compared with the fitness of offspring emerged from hosts rejected several times before being accepted for oviposition. 4. The pattern of host acceptance and rejection was not related to any of the measured fitness parameters of the offspring emerging from these hosts (development time, size at emergence, sex ratio at emergence, and female offspring egg load). 5. While complex post facto adaptive explanations can be devised to explain the nature of such a time and energy consuming host selection process, it is suggested that physiological constraints on egg production or oviposition may provide an alternative, purely mechanistic, explanation for the results obtained. [source] Does Booby Egg Dumping Amount to Quasi-Parasitism?ETHOLOGY, Issue 7 2006Marcela Osorio-Beristain Quasi-parasitism occurs when a paired male facilitates dumping in its own nest by an extra-pair female with which it has recently copulated. Although numerous observations hint at quasi-parasitism in diverse avian species, direct behavioral confirmation of male complicity is required to exclude the alternative adaptive explanations enumerated by Griffith et al. [Behav. Ecol. Sociobiol.56 (2004) 191]. Our direct observations on dumping by female blue-footed boobies (Sula nebouxii) show apparent male ambivalence: males were hostile to eggs dumped by their extra-pair partners but half-hearted in repelling those partners after the act of dumping. Hostility was evidenced when a host male that was present during dumping destroyed the extra-pair partner's egg and when extra-pair partners selectively dumped when the host male was absent or distracted rather than when it was alone on the territory. Host males appear to deter dumping by their extra-pair partners rather than facilitating it, and their partial tolerance of females that have dumped may be a result of their general tolerance of unaccompanied females. Although paired male boobies sometimes copulate with females that dump into their nests, apparently this is not quasi-parasitism. [source] EVOLUTION OF COLOR VARIATION IN DRAGON LIZARDS: QUANTITATIVE TESTS OF THE ROLE OF CRYPSIS AND LOCAL ADAPTATIONEVOLUTION, Issue 7 2004Devi M. Stuart-Fox Abstract Many animal species display striking color differences with respect to geographic location, sex, and body region. Traditional adaptive explanations for such complex patterns invoke an interaction between selection for conspicuous signals and natural selection for crypsis. Although there is now a substantial body of evidence supporting the role of sexual selection for signaling functions, quantitative studies of crypsis remain comparatively rare. Here, we combine objective measures of coloration with information on predator visual sensitivities to study the role of crypsis in the evolution of color variation in an Australian lizard species complex (Ctenophorus decresii). We apply a model that allows us to quantify crypsis in terms of the visual contrast of the lizards against their natural backgrounds, as perceived by potential avian predators. We then use these quantitative estimates of crypsis to answer the following questions. Are there significant differences in crypsis conspicuousness among populations? Are there significant differences in crypsis conspicuousness between the sexes? Are body regions "exposed" to visual predators more cryptic than "hidden" body regions? Is there evidence for local adaptation with respect to crypsis against different substrates? In general, our results confirmed that there are real differences in crypsis conspicuousness both between populations and between sexes; that exposed body regions were significantly more cryptic than hidden ones, particularly in females; and that females, but not males, are more cryptic against their own local background than against the background of other populations. Body regions that varied most in contrast between the sexes and between populations were also most conspicuous and are emphasized by males during social and sexual signaling. However, results varied with respect to the aspect of coloration studied. Results based on chromatic contrast ("hue' of color) provided better support for the crypsis hypothesis than did results based on achromatic contrast ("brightness' of color). Taken together, these results support the view that crypsis plays a substantial role in the evolution of color variation and that color patterns represent a balance between the need for conspicuousness for signaling and the need for crypsis to avoid predation. [source] Avian eggshell coloration: new perspectives on adaptive explanationsBIOLOGICAL JOURNAL OF THE LINNEAN SOCIETY, Issue 4 2010MICHAEL I. CHERRY Recent work suggests that the evolution of egg coloration may have been constrained in three important ways that have not yet been critically synthesized in any review. First, on account of birds being able to see in the ultraviolet spectrum, the interaction between the properties of avian vision and the light environment of nests imply different perceptions of egg coloration from those experienced by humans. Second, a new hypothesis to explain blue,green egg coloration interprets it as a sexually selected signal to males of the laying female's genetic quality. Third, evidence from taxa as divergent as sparrowhawks and great tits indicates that protoporphyrin pigments responsible for maculation (spotting patterns) have a structural function in compensating for eggshell thinning, as caused by calcium stress, and, more recently, dichlorodiphenyltrichloroethane. We consider this to be the most convincing explanation for the primary function of spotting, although an important secondary function might arise through the fact that individual patterns of maculation may allow birds to identify their own eggs, effectively serving as signatures in the face of inter- or intra-specific brood parasitism. These constraints or hypotheses are not mutually exclusive, and should not be taken to imply that one, but not other, agents of selection might apply to any one species. However, the sexually-selected eggshell coloration hypothesis is least plausible for hole-nesting birds because of the poor light quality available, although such species have been the focus of research in this area, and only a single experimental study has shown a link between egg coloration and male provisioning. Furthermore, the observed relationships between female phenotypic quality and egg traits do not necessarily imply that they have signalling functions. © 2010 The Linnean Society of London, Biological Journal of the Linnean Society, 2010, 100, 753,762. [source] Hatching asynchrony and growth trade-offs within domesticated and wild zebra finch, Taeniopygia guttata, broodsBIOLOGICAL JOURNAL OF THE LINNEAN SOCIETY, Issue 4 2010MARK C. MAINWARING The Australian zebra finch, Taeniopygia guttata, is a widely used model organism, yet few studies have compared domesticated and wild birds with the aim of examining its relevance as an evolutionary model species. Domestic and wild broods hatch over approximately 4 and 2 days, respectively, which is important given that nestlings can fledge after as little as 12 days, although 16,18 days is common. We aimed to evaluate the extent to which the greater hatching asynchrony in domestic stock may effect reproductive success through greater variance in size hierarchies, variance in within-brood growth rates, and partial brood mortality. Therefore, by simultaneously controlling brood sizes and experimentally manipulating hatching intervals in both domesticated and wild birds, we investigated the consequences of hatching intervals for fledging success and nestling growth patterns, as well as trade-offs. Fledging success was similarly high in domestic and wild broods of either hatching pattern. Nonetheless, between-brood analyses revealed that domestic nestlings had significantly higher masses, larger skeletal characters, and longer wings than their wild counterparts, although wild nestlings had comparable wing lengths at the pre-fledging stage. Moreover, within-brood analyses revealed only negligible differences between domestic and wild nestlings, and larger effects of hatching order and hatching pattern. Therefore, despite significant differences in the hatching intervals, and the ultimate size achieved by nestlings, the domestication process does not appear to have significantly altered nestling growth trade-offs. The present study provides reassuring evidence that studies involving domesticated zebra finches, or other domesticated model organisms, may provide reasonable adaptive explanations in behavioural and evolutionary ecology. © 2010 The Linnean Society of London, Biological Journal of the Linnean Society, 2010, 100, 763,773. [source] ,O sibling, where art thou?'- a review of avian sibling recognition with respect to the mammalian literatureBIOLOGICAL REVIEWS, Issue 1 2004Shinichi Nakagawa ABSTRACT Avian literature on sibling recognition is rare compared to that developed by mammalian researchers. We compare avian and mammalian research on sibling recognition to identify why avian work is rare, how approaches differ and what avian and mammalian researchers can learn from each other. Three factors: (1) biological differences between birds and mammals, (2) conceptual biases and (3) practical constraints, appear to influence our current understanding. Avian research focuses on colonial species because sibling recognition is considered adaptive where,mixing potential'of dependent young is high; research on a wide range of species, breeding systems and ecological conditions is now needed. Studies of acoustic recognition cues dominate avian literature; other types of cues (e.g. visual, olfactory) deserve further attention. The effect of gender on avian sibling recognition has yet to be investigated; mammalian work shows that gender can have important influences. Most importantly, many researchers assume that birds recognise siblings through,direct familiarisation'(commonly known as associative learning or familiarity); future experiments should also incorporate tests for,indirect familiarisation'(commonly known as phenotype matching). If direct familiarisation proves crucial, avian research should investigate how periods of separation influence sibling discrimination. Mammalian researchers typically interpret sibling recognition in broad functional terms (nepotism, optimal outbreeding); some avian researchers more successfully identify specific and testable adaptive explanations, with greater relevance to natural contexts. We end by reporting exciting discoveries from recent studies of avian sibling recognition that inspire further interest in this topic. [source] | ||||||||||