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      Sexual dimorphism in the badlands cricket (Orthoptera, Gryllinae, Gryllus personatus)

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      Journal of Orthoptera Research
      Pensoft Publishers

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          Abstract

          Sexual dimorphism (SD) is a common phenomenon in sexual species and can manifest in a variety of ways. Sexual size dimorphism (SSD) is commonly investigated, but it can be confounded with sexual shape dimorphism (SShD) if multivariate measures of size are not used. Univariate studies may also overestimate the prevalence or direction of SSD when the sexes are strikingly different in shape, which may be an issue in taxa such as Orthoptera and other terrestrial arthropods where maximum body size is strongly constrained. Here we tested for the occurrence of both SSD and SShD in the badlands cricket Gryllus personatus (Orthoptera, Gryllinae). We measured four body size dimensions—maxillae span, head width, pronotum length, and mean hind femur length—and used multivariate methods to test whether male and female adult badlands crickets were sexually dimorphic in size and/or shape. All the univariate dimensions were sexually dimorphic, with males having wider heads and maxillae than females and females having longer pronota and hind femora than males, which indicates SShD. However, multivariate methods failed to detect SSD, instead confirming that the sexes primarily differ in body shape. We show how a simple ratio of head width to pronotum length captures SShD in badlands crickets and apply it to iNaturalist, a citizen science platform, to broaden our findings. We propose that orthopterists studying SD minimally measure head width, pronotum length, and hind femur length as a standard that will allow a more repeatable and generalizable assessment of the prevalence and direction of both SSD and SShD.

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          Sexual Selection

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            Parental investment, sexual selection and sex ratios.

            Conventional sex roles imply caring females and competitive males. The evolution of sex role divergence is widely attributed to anisogamy initiating a self-reinforcing process. The initial asymmetry in pre-mating parental investment (eggs vs. sperm) is assumed to promote even greater divergence in post-mating parental investment (parental care). But do we really understand the process? Trivers [Sexual Selection and the Descent of Man 1871-1971 (1972), Aldine Press, Chicago] introduced two arguments with a female and male perspective on whether to care for offspring that try to link pre-mating and post-mating investment. Here we review their merits and subsequent theoretical developments. The first argument is that females are more committed than males to providing care because they stand to lose a greater initial investment. This, however, commits the 'Concorde Fallacy' as optimal decisions should depend on future pay-offs not past costs. Although the argument can be rephrased in terms of residual reproductive value when past investment affects future pay-offs, it remains weak. The factors likely to change future pay-offs seem to work against females providing more care than males. The second argument takes the reasonable premise that anisogamy produces a male-biased operational sex ratio (OSR) leading to males competing for mates. Male care is then predicted to be less likely to evolve as it consumes resources that could otherwise be used to increase competitiveness. However, given each offspring has precisely two genetic parents (the Fisher condition), a biased OSR generates frequency-dependent selection, analogous to Fisherian sex ratio selection, that favours increased parental investment by whichever sex faces more intense competition. Sex role divergence is therefore still an evolutionary conundrum. Here we review some possible solutions. Factors that promote conventional sex roles are sexual selection on males (but non-random variance in male mating success must be high to override the Fisher condition), loss of paternity because of female multiple mating or group spawning and patterns of mortality that generate female-biased adult sex ratios (ASR). We present an integrative model that shows how these factors interact to generate sex roles. We emphasize the need to distinguish between the ASR and the operational sex ratio (OSR). If mortality is higher when caring than competing this diminishes the likelihood of sex role divergence because this strongly limits the mating success of the earlier deserting sex. We illustrate this in a model where a change in relative mortality rates while caring and competing generates a shift from a mammalian type breeding system (female-only care, male-biased OSR and female-biased ASR) to an avian type system (biparental care and a male-biased OSR and ASR).
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              Behavioral Causes and Consequences of Sexual Size Dimorphism

                Author and article information

                Contributors
                (View ORCID Profile)
                Journal
                Journal of Orthoptera Research
                JOR
                Pensoft Publishers
                1937-2426
                1082-6467
                June 12 2023
                June 12 2023
                : 32
                : 2
                : 119-126
                Article
                10.3897/jor.32.93513
                7652f5ff-4afd-4e2d-b823-9d6332fe9974
                © 2023

                http://creativecommons.org/licenses/by/4.0/

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