21 research outputs found

    Ecological character displacement in the face of gene flow: Evidence from two species of nightingales

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    <p>Abstract</p> <p>Background</p> <p>Ecological character displacement is a process of phenotypic differentiation of sympatric populations caused by interspecific competition. Such differentiation could facilitate speciation by enhancing reproductive isolation between incipient species, although empirical evidence for it at early stages of divergence when gene flow still occurs between the species is relatively scarce. Here we studied patterns of morphological variation in sympatric and allopatric populations of two hybridizing species of birds, the Common Nightingale (<it>Luscinia megarhynchos</it>) and the Thrush Nightingale (<it>L. luscinia</it>).</p> <p>Results</p> <p>We conducted principal component (PC) analysis of morphological traits and found that nightingale species converged in overall body size (PC1) and diverged in relative bill size (PC3) in sympatry. Closer analysis of morphological variation along geographical gradients revealed that the convergence in body size can be attributed largely to increasing body size with increasing latitude, a phenomenon known as Bergmann's rule. In contrast, interspecific interactions contributed significantly to the observed divergence in relative bill size, even after controlling for the effects of geographical gradients. We suggest that the divergence in bill size most likely reflects segregation of feeding niches between the species in sympatry.</p> <p>Conclusions</p> <p>Our results suggest that interspecific competition for food resources can drive species divergence even in the face of ongoing hybridization. Such divergence may enhance reproductive isolation between the species and thus contribute to speciation.</p

    Fluoride concentrations in the pineal gland, brain and bone of goosander (Mergus merganser) and its prey in Odra River estuary in Poland

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    Novel genetic associations for blood pressure identified via gene-alcohol interaction in up to 570K individuals across multiple ancestries

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    Heavy alcohol consumption is an established risk factor for hypertension; the mechanism by which alcohol consumption impact blood pressure (BP) regulation remains unknown. We hypothesized that a genome-wide association study accounting for gene-alcohol consumption interaction for BP might identify additional BP loci and contribute to the understanding of alcohol-related BP regulation. We conducted a large two-stage investigation incorporating joint testing of main genetic effects and single nucleotide variant (SNV)-alcohol consumption interactions. In Stage 1, genome-wide discovery meta-analyses in approximate to 131 K individuals across several ancestry groups yielded 3,514 SNVs (245 loci) with suggestive evidence of association (P <1.0 x 10(-5)). In Stage 2, these SNVs were tested for independent external replication in individuals across multiple ancestries. We identified and replicated (at Bonferroni correction threshold) five novel BP loci (380 SNVs in 21 genes) and 49 previously reported BP loci (2,159 SNVs in 109 genes) in European ancestry, and in multi-ancestry meta-analyses (P < 5.0 x 10(-8)). For African ancestry samples, we detected 18 potentially novel BP loci (P< 5.0 x 10(-8)) in Stage 1 that warrant further replication. Additionally, correlated meta-analysis identified eight novel BP loci (11 genes). Several genes in these loci (e.g., PINX1, GATA4, BLK, FTO and GABBR2 have been previously reported to be associated with alcohol consumption. These findings provide insights into the role of alcohol consumption in the genetic architecture of hypertension

    Forecasting Large-Scale Habitat Suitability of European Bustards under Climate Change: The Role of Environmental and Geographic Variables

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    Distribution of the great and the little bustard in the study area that comprises the majority of Europe, North Africa and Southwest Asia according to Hagemeijer & Blair (1997), Eken & Magnin (2000), Alonso et al. (2005) and Palacin & Alonso (2009). Regarding climatic variables, raw temperature and precipitation data were extracted from WorldClim (http://www.worldclim.org/) according to the Climgen Statistical Downscaling for the ‘current’ period 1961-1990 and for the future periods 2050 and 2080, the latter periods according to the emission scenario A1B in three different general circulation models (GCMs): CGCM31, ECHAM5 and HADCM3. We calculated three bioclimatic variables: cumulative annual rainfall, temperature range between July and January, and the mean temperature during the reproductive period for both species, i.e. between April and July. We also obtained the mean slope of the UTM cell (derived from GLOBE et al. 1999) and the percentage of dry crops and pasturelands in each cell (obtained from the USGS Land Cover, http://edc2.usgs.gov/glcc/glcc.php). Additionally, we included the mean value of human population density (obtained from ORNL 2009).Distribution of the great and the little bustard and values of environmental and geographic variables in each 50 km x 50 km UTM cell of the Western Palearctic.Peer reviewe
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