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Vertebrate Groups (vertebrate + groups)
Selected AbstractsA mutation in the zebrafish Na,K-ATPase subunit atp1a1a.1 provides genetic evidence that the sodium potassium pump contributes to left-right asymmetry downstream or in parallel to nodal flowDEVELOPMENTAL DYNAMICS, Issue 7 2006Elin Ellertsdottir Abstract While there is a good conceptual framework of dorsoventral and anterioposterior axes formation in most vertebrate groups, understanding of left-right axis initiation is fragmentary. Diverse mechanisms have been implied to contribute to the earliest steps of left-right asymmetry, including small molecule signals, gap junctional communication, membrane potential, and directional flow of extracellular liquid generated by monocilia in the node region. Here we demonstrate that a mutation in the zebrafish Na,K-ATPase subunit atp1a1a causes left-right defects including isomerism of internal organs at the anatomical level. The normally left-sided Nodal signal spaw as well as its inhibitor lefty are expressed bilaterally, while pitx2 may appear random or bilateral. Monocilia movement and fluid circulation in Kupffer's vesicle are normal in atp1a1am883 mutant embryos. Therefore, the Na,K-ATPase is required downstream or in parallel to monocilia function during initiation of left-right asymmetry in zebrafish. Developmental Dynamics 235:1794,1808, 2006. © 2006 Wiley-Liss, Inc. [source] Factors controlling the spatial species richness pattern of four groups of terrestrial vertebrates in an area between two different biogeographic regions in northern SpainJOURNAL OF BIOGEOGRAPHY, Issue 4 2004David Nogués-Bravo Abstract Aim, To examine the influence of environmental variables on species richness patterns of amphibians, reptiles, mammals and birds and to assess the general usefulness of regional atlases of fauna. Location, Navarra (10,421 km2) is located in the north of the Iberian Peninsula, in a territory shared by Mediterranean and Eurosiberian biogeographic regions. Important ecological patterns, climate, topography and land-cover vary significantly from north to south. Methods, Maps of vertebrate distribution and climatological and environmental data bases were used in a geographic information systems framework. Generalized additive models and partial regression analysis were used as statistical tools to differentiate (A) the purely spatial fraction, (B) the spatially structured environmental fraction and (C) the purely environmental fraction. In this way, we can evaluate the explanatory capacity of each variable, avoiding false correlations and assessing true causality. Final models were obtained through a stepwise procedure. Results, Energy-related features of climate, aridity and land-cover variables show significant correlation with the species richness of reptiles, mammals and birds. Mammals and birds exhibit a spatial pattern correlated with variables such as aridity index and vegetation land-cover. However, the high values of the spatially structured environmental fraction B and the low values of the purely environmental fraction A suggest that these predictor variables have a limited causal relationship with species richness for these vertebrate groups. An increment in land-cover diversity is correlated with an increment of specific richness in reptiles, mammals and birds. No variables were found to be statistically correlated with amphibian species richness. Main conclusions, Although aridity and land-cover are the best predictor variables, their causal relationship with species richness must be considered with caution. Historical factors exhibiting a similar spatial pattern may be considered equally important in explaining the patterns of species richness. Also, land-cover diversity appears as an important factor for maintaining biological diversity. Partial regression analysis has proved a useful technique in dealing with spatial autocorrelation. These results highlight the usefulness of coarsely sampled data and cartography at regional scales to predict and explain species richness patterns for mammals and birds. The accuracy of models appears to be related to the range perception of each group and the scale of the information. [source] The evolution of teleost pigmentation and the fish-specific genome duplicationJOURNAL OF FISH BIOLOGY, Issue 8 2008I. Braasch Teleost fishes have evolved a unique complexity and diversity of pigmentation and colour patterning that is unmatched among vertebrates. Teleost colouration is mediated by five different major types of neural-crest derived pigment cells, while tetrapods have a smaller repertoire of such chromatophores. The genetic basis of teleost colouration has been mainly uncovered by the cloning of pigmentation genes in mutants of zebrafish Danio rerio and medaka Oryzias latipes. Many of these teleost pigmentation genes were already known as key players in mammalian pigmentation, suggesting partial conservation of the corresponding developmental programme among vertebrates. Strikingly, teleost fishes have additional copies of many pigmentation genes compared with tetrapods, mainly as a result of a whole-genome duplication that occurred 320,350 million years ago at the base of the teleost lineage, the so-called fish-specific genome duplication. Furthermore, teleosts have retained several duplicated pigmentation genes from earlier rounds of genome duplication in the vertebrate lineage, which were lost in other vertebrate groups. It was hypothesized that divergent evolution of such duplicated genes may have played an important role in pigmentation diversity and complexity in teleost fishes, which therefore not only provide important insights into the evolution of the vertebrate pigmentary system but also allow us to study the significance of genome duplications for vertebrate biodiversity. [source] The Development of the Epicardium in the Sturgeon Acipenser naccariiTHE ANATOMICAL RECORD : ADVANCES IN INTEGRATIVE ANATOMY AND EVOLUTIONARY BIOLOGY, Issue 10 2009José M. Icardo Abstract This article reports on the development of the epicardium in alevins of the sturgeon Acipenser naccarii, aged 4,25 days post-hatching (dph). Epicardial development starts at 4 dph with formation of the proepicardium (PE) that arises as a bilateral structure at the boundary between the sinus venosus and the duct of Cuvier. The PE later becomes a midline organ arising from the wall of the sinus venosus and ending at the junction between the liver, the sinus venosus and the transverse septum. This relative displacement appears related to venous reorganization at the caudal pole of the heart. The mode and time of epicardium formation is different in the various heart chambers. The conus epicardium develops through migration of a cohesive epithelium from the PE villi, and is completed through bleb-like aggregates detached from the PE. The ventricular epicardium develops a little later, and mostly through bleb-like aggregates. The bulbus epicardium appears to derive from the mesothelium located at the junction between the outflow tract and the pericardial cavity. Strikingly, formation of the epicardium of the atrium and the sinus venosus is a very late event occurring after the third month of development. Associated to the PE, a sino-ventricular ligament develops as a permanent connection. This ligament contains venous vessels that communicate the subepicardial coronary plexus and the sinus venosus, and carries part of the heart innervation. The development of the sturgeon epicardium shares many features with that of other vertebrate groups. This speaks in favour of conservative mechanisms across the evolutionary scale. Anat Rec, 2009. © 2009 Wiley-Liss, Inc. [source] Predicted impact of climate change on threatened terrestrial vertebrates in central Spain highlights differences between endotherms and ectothermsANIMAL CONSERVATION, Issue 4 2010P. Aragón Abstract Climate change can induce shifts in species ranges. Of special interest are range shifts in regions with a conflict of interest between land use and the conservation of threatened species. Here we focus on the 94 threatened terrestrial vertebrates occurring in the Madrid region (Central Spain) and model their distributions using data for the whole peninsular Spain to evaluate which vertebrate groups are likely to be more sensitive to climatic change. First, we generated predictive models to quantify the extent to which species distributions are explained by current climate. We then extrapolated the models temporally to predict the effects of two climate-change scenarios on species distributions. We also examined the impact on a recently proposed reserve relative to other interconnected zones with lower protection status but categorized as Areas of Community Importance by the European Union. The variation explained by climatic predictors was greater in ectotherms. The change in species composition differed between the proposed reserve and the other protected areas. Endothermic and ectothermic vertebrates had different patterns of changes in species composition but those of ectotherms matched with temperature departures predicted by climate change. Our results, together with the limited dispersal capacity of herptiles, suggest that trade-offs between different design criteria accounting for animal group differences are necessary for reserve selection. [source] Insects ,Down Under', Diversity, endemism and evolution of the Australian insect fauna: examples from select ordersAUSTRALIAN JOURNAL OF ENTOMOLOGY, Issue 3 2004Andrew D Austin In addition, a number of groups are noticeably absent or depauperate on the continent. Many groups found in Australia show characteristic Gondwanan distribution patterns on the southern continents. There are extensive radiations on the plant families Myrtaceae and Mimosaceae, a specialised arid/semiarid fauna, and diverse taxa associated with rainforests and seasonally wet tropical regions. The fauna is also poorly studied, particularly when compared with the flora and vertebrate groups. However, studies in the last two decades have provided a more comprehensive picture of the size of the fauna, relationships, levels of endemism, origins and its evolution. Here we provide an overview of these and other aspects of Australian insect diversity, focusing on six groups, the Thysanoptera and the five megadiverse orders Hemiptera, Coleoptera, Diptera, Lepidoptera and Hymenoptera. [source] Testing co-evolutionary hypotheses over geological timescales: interactions between Mesozoic non-avian dinosaurs and cycadsBIOLOGICAL REVIEWS, Issue 1 2009Richard J. Butler Abstract The significance of co-evolution over ecological timescales is well established, yet it remains unclear to what extent co-evolutionary processes contribute to driving large-scale evolutionary and ecological changes over geological timescales. Some of the most intriguing and pervasive long-term co-evolutionary hypotheses relate to proposed interactions between herbivorous non-avian dinosaurs and Mesozoic plants, including cycads. Dinosaurs have been proposed as key dispersers of cycad seeds during the Mesozoic, and temporal variation in cycad diversity and abundance has been linked to dinosaur faunal changes. Here we assess the evidence for proposed hypotheses of trophic and evolutionary interactions between these two groups using diversity analyses, a new database of Cretaceous dinosaur and plant co-occurrence data, and a geographical information system (GIS) as a visualisation tool. Phylogenetic evidence suggests that the origins of several key biological properties of cycads (e.g. toxins, bright-coloured seeds) likely predated the origin of dinosaurs. Direct evidence of dinosaur,cycad interactions is lacking, but evidence from extant ecosystems suggests that dinosaurs may plausibly have acted as seed dispersers for cycads, although it is likely that other vertebrate groups (e.g. birds, early mammals) also played a role. Although the Late Triassic radiations of dinosaurs and cycads appear to have been approximately contemporaneous, few significant changes in dinosaur faunas coincide with the late Early Cretaceous cycad decline. No significant spatiotemporal associations between particular dinosaur groups and cycads can be identified , GIS visualisation reveals disparities between the spatiotemporal distributions of some dinosaur groups (e.g. sauropodomorphs) and cycads that are inconsistent with co-evolutionary hypotheses. The available data provide no unequivocal support for any of the proposed co-evolutionary interactions between cycads and herbivorous dinosaurs , diffuse co-evolutionary scenarios that are proposed to operate over geological timescales are plausible, but such hypotheses need to be firmly grounded on direct evidence of interaction and may be difficult to support given the patchiness of the fossil record. [source] | ||||||||||