RESUMO
The composition of mammalian gut microbiomes is highly conserved within species, yet the mechanisms by which microbiome composition is transmitted and maintained within lineages of wild animals remain unclear. Mutually compatible hypotheses exist, including that microbiome fidelity results from inherited dietary habits, shared environmental exposure, morphophysiological filtering and/or maternal effects. Interspecific hybrids are a promising system in which to interrogate the determinants of microbiome composition because hybrids can decouple traits and processes that are otherwise co-inherited in their parent species. We used a population of free-living hybrid zebras (Equus quagga × grevyi) in Kenya to evaluate the roles of these four mechanisms in regulating microbiome composition. We analysed faecal DNA for both the trnL-P6 and the 16S rRNA V4 region to characterize the diets and microbiomes of the hybrid zebra and of their parent species, plains zebra (E. quagga) and Grevy's zebra (E. grevyi). We found that both diet and microbiome composition clustered by species, and that hybrid diets and microbiomes were largely nested within those of the maternal species, plains zebra. Hybrid microbiomes were less variable than those of either parent species where they co-occurred. Diet and microbiome composition were strongly correlated, although the strength of this correlation varied between species. These patterns are most consistent with the maternal-effects hypothesis, somewhat consistent with the diet hypothesis, and largely inconsistent with the environmental-sourcing and morphophysiological-filtering hypotheses. Maternal transmittance likely operates in conjunction with inherited feeding habits to conserve microbiome composition within species.
Assuntos
Dieta , Equidae , Fezes , Microbioma Gastrointestinal , RNA Ribossômico 16S , Animais , RNA Ribossômico 16S/genética , Quênia , Fezes/microbiologia , Microbioma Gastrointestinal/genética , Equidae/microbiologia , Hibridização Genética , Feminino , Microbiota/genética , MasculinoRESUMO
The ability to recognize mates, kin, offspring and neighbors by their individually distinctive traits-individual recognition (IR)-is widespread in animals. Much work has investigated IR from the perspective of the recognizer, but less is known about the extent to which signals have evolved to facilitate IR. To explore this, one approach is to compare putative identity signals among species that differ in life history and extent of IR. In Common Murres (Uria aalge), a colonially breeding seabird, the eggs of individual females are remarkably variable in terms of color and pattern (maculation). Common Murres also appear to recognize their own eggs, leading to the hypothesis that variable egg phenotypes evolved to promote recognizability. However, we lack a quantitative assessment of the egg pattern information in Common Murres and their close relatives. Here, we analyzed images of eggs laid by four alcid species: Common Murres, Thick-billed Murres (Uria lomvia), Razorbills (Alca torda) and Dovekies (Alle alle). We extracted pattern measures believed to be relevant to bird vision and calculated Beecher's information statistic (Hs ), which allowed us to compare the amount of identity information contained in each species' egg patterns. Murres, which nest in dense colonies and can recognize their own eggs, have egg patterns with a relatively large amount of identity information compared to Razorbills and Dovekies. Egg recognition has not been demonstrated in Razorbills and Dovekies, whose colonies are less dense. Our results are consistent with the hypothesis that complex patterns of Murre eggs may have evolved to increase individual recognizability.
Assuntos
Charadriiformes , Óvulo , Animais , FemininoRESUMO
Animal communication is inherently spatial. Both signal transmission and signal reception have spatial biases-involving direction, distance, and position-that interact to determine signaling efficacy. Signals, be they visual, acoustic, or chemical, are often highly directional. Likewise, receivers may only be able to detect signals if they arrive from certain directions. Alignment between these directional biases is therefore critical for effective communication, with even slight misalignments disrupting perception of signaled information. In addition, signals often degrade as they travel from signaler to receiver, and environmental conditions that impact transmission can vary over even small spatiotemporal scales. Thus, how animals position themselves during communication is likely to be under strong selection. Despite this, our knowledge regarding the spatial arrangements of signalers and receivers during communication remains surprisingly coarse for most systems. We know even less about how signaler and receiver behaviors contribute to effective signaling alignment over time, or how signals themselves may have evolved to influence and/or respond to these aspects of animal communication. Here, we first describe why researchers should adopt a more explicitly geometric view of animal signaling, including issues of location, direction, and distance. We then describe how environmental and social influences introduce further complexities to the geometry of signaling. We discuss how multimodality offers new challenges and opportunities for signalers and receivers. We conclude with recommendations and future directions made visible by attention to the geometry of signaling.
Assuntos
Comunicação Animal , AnimaisRESUMO
The use of artificially coloured stimuli, especially to test hypotheses about sexual selection and anti-predator defence, has been common in behavioural ecology since the pioneering work of Tinbergen. To investigate the effects of colour on animal behaviour, many researchers use paints, markers and dyes to modify existing colours or to add colour to synthetic models. Because colour perception varies widely across species, it is critical to account for the signal receiver's vision when performing colour manipulations. To explore this, we applied 26 typical coloration products to different types of avian feathers. Next, we measured the artificially coloured feathers using two complementary techniques-spectrophotometry and digital ultraviolet--visible photography-and modelled their appearance to mammalian dichromats (ferret, dog), trichromats (honeybee, human) and avian tetrachromats (hummingbird, blue tit). Overall, artificial colours can have dramatic and sometimes unexpected effects on the reflectance properties of feathers, often differing based on feather type. The degree to which an artificial colour differs from the original colour greatly depends on an animal's visual system. 'White' paint to a human is not 'white' to a honeybee or blue tit. Based on our analysis, we offer practical guidelines for reducing the risk of introducing unintended effects when using artificial colours in behavioural experiments.