RESUMO
AbstractInsular land crabs (Gecarcinidae) can transit between terrestrial and aquatic environments and inhabit vacant ecological niches that other species do not occupy in oceanic islands. During the reproductive period, these crabs migrate between residential and reproductive areas; this is a critical moment because individuals are more vulnerable to stressful conditions, especially species occupying anthropized islands. Currently, many insular crab species are considered threatened; yet few studies have evaluated the biology of this group, especially the size at which individuals reach sexual maturity. Here, we evaluate the size at the onset of morphological, physiological, and functional maturity for the insular land crab Johngarthia lagostoma in Trindade Island (Brazil) and assess the chronology of the events underlying those processes. Males and females exhibited the same order of occurrence of the different maturity processes, starting by being morphologically, physiologically, and, finally, functionally mature at similar sizes (about 56 mm carapace width). This value corresponds to at least half of the maximum size that J. lagostoma reaches in Trindade Island and is close to the average relative value registered to other Gecarcinidae species. Considering the current decline in the population of insular crabs, such estimates can be used in management programs, mainly for the definition and protection of breeding and recruitment areas. Specifically, our results can be used toward the conservation of J. lagostoma, which is currently classified as endangered in Brazil, especially in the isolated population of Trindade Island.
Assuntos
Braquiúros , Animais , Braquiúros/fisiologia , Brasil , Ecossistema , Feminino , Humanos , Masculino , Reprodução/fisiologiaRESUMO
Modular organization provides flexibility for colonial animals to deal with variable and unpredictable environmental conditions since each module has specific tasks within the colony, such as feeding, defending or reproducing. Depending on the selecting pressures, sessile organisms may phenotypically adjust the morphology of each module or modify their density, increasing individual fitness. Here we used the marine bryozoan Schizoporella errata (Cheilostomata, Schizoporellidae) to test how the divergent conditions between two artificial habitats, the location inside a marina (IM) and the external wall of the breakwater (BW), affect colony size and the density of the distinct modules. The density of avicularia and ovicells, modules related to defense and reproduction, respectively, did not differ between habitats. However, colonies growing in the turbulent waters of BW were, in general, larger and had higher density of feeding autozooids than those at IM. Reciprocal transplants of bryozoan clones indicated that trait variation is genotype-dependent but varies according to the environmental conditions at the assigned location. The occurrence of larger colonies with more zooids in BW is probably linked to the easier feeding opportunity offered by the small diffusive boundary layer around the colony at this location. Since in colonial polymorphic organisms each module (zooid) performs a specific function, the phenotypic response is not uniform across colonies, affecting only those modules that are susceptible to variations in the main selective pressures. Understanding the importance of colony-level plasticity is relevant to predict how modularity will contribute to organisms to deal with human-induced environmental changes in coastal habitats.
Assuntos
Briozoários/anatomia & histologia , Ecossistema , Animais , Organismos Aquáticos , Briozoários/genética , Briozoários/crescimento & desenvolvimento , Briozoários/fisiologiaRESUMO
Animals from a wide range of taxonomic groups are capable of colour change, of which camouflage is one of the main functions. A considerable amount of past work on this subject has investigated species capable of extremely rapid colour change (in seconds). However, relatively slow colour change (over hours, days, weeks and months), as well as changes arising via developmental plasticity are probably more common than rapid changes, yet less studied. We discuss three key areas of colour change and camouflage. First, we review the mechanisms underpinning colour change and developmental plasticity for camouflage, including cellular processes, visual feedback, hormonal control and dietary factors. Second, we discuss the adaptive value of colour change for camouflage, including the use of different camouflage types. Third, we discuss the evolutionary-ecological implications of colour change for concealment, including what it can tell us about intraspecific colour diversity, morph-specific strategies, and matching to different environments and microhabitats. Throughout, we discuss key unresolved questions and present directions for future work, and highlight how colour change facilitates camouflage among habitats and arises when animals are faced with environmental changes occurring over a range of spatial and temporal scales.This article is part of the themed issue 'Animal coloration: production, perception, function and application'.
Assuntos
Adaptação Biológica , Evolução Biológica , Mimetismo Biológico , Cor , AnimaisRESUMO
BACKGROUND: Colour and shape polymorphisms are important features of many species and may allow individuals to exploit a wider array of habitats, including through behavioural differences among morphs. In addition, differences among individuals in behaviour and morphology may reflect different strategies, for example utilising different approaches to camouflage. Hippolyte obliquimanus is a small shrimp species inhabiting different shallow-water vegetated habitats. Populations comprise two main morphs: homogeneous shrimp of variable colour (H) and transparent individuals with coloured stripes (ST). These morphs follow different distribution patterns between their main algal habitats; the brown weed Sargassum furcatum and the pink-red weed Galaxaura marginata. In this study, we first investigated morph-specific colour change and habitat selection, as mechanisms underlying camouflage and spatial distribution patterns in nature. Then, we examined habitat fidelity, mobility, and morphological traits, further indicating patterns of habitat use. RESULTS: H shrimp are capable of changing colour in just a few days towards their algal background, achieving better concealment in the more marginal, and less preferred, red weed habitat. Furthermore, laboratory trials showed that habitat fidelity is higher for H shrimp, whereas swimming activity is higher for the ST morph, aligned to morphological evidence indicating these two morphs comprise a more benthic (H) and a more pelagic (ST) life-style, respectively. CONCLUSIONS: Results suggest that H shrimp utilise a camouflage strategy specialised to a limited number of backgrounds at any one time, whereas ST individuals comprise a phenotype with more generalist camouflage (transparency) linked to a more generalist background utilisation. The coexistence within a population of distinct morphotypes with apparently alternative strategies of habitat use and camouflage may reflect differential responses to substantial seasonal changes in macroalgal cover. Our findings also demonstrate how colour change, behaviour, morphology, and background use all interact in achieving camouflage.