2 research outputs found

    Short-lived species move uphill faster under climate change

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    Climate change is pushing species ranges and abundances towards the poles and mountain tops. Although many studies have documented local altitudinal shifts, knowledge of general patterns at a large spatial scale, such as a whole mountain range, is scarce. From a conservation perspective, studying altitudinal shifts in wildlife is relevant because mountain regions often represent biodiversity hotspots and are among the most vulnerable ecosystems. Here, we examine whether altitudinal shifts in birds' abundances have occurred in the Scandinavian mountains over 13 years, and assess whether such shifts are related to species' traits. Using abundance data, we show a clear pattern of uphill shift in the mean altitude of bird abundance across the Scandinavian mountains, with an average speed of 0.9 m per year. Out of 76 species, 7 shifted significantly their abundance uphill. Altitudinal shift was strongly related to species' longevity: short-lived species showed more pronounced uphill shifts in abundance than long-lived species. The observed abundance shifts suggest that uphill shifts are not only driven by a small number of individuals at the range boundaries, but the overall bird abundances are on the move. Overall, the results underscore the wide-ranging impact of climate change and the potential vulnerability of species with slow life histories, as they appear less able to timely respond to rapidly changing climatic conditions.Peer reviewe

    Common variants near CAV1 and CAV2 are associated with primary open-angle glaucoma

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    We conducted a genome-wide association study for primary open-angle glaucoma (POAG) in 1,263 affected individuals (cases) and 34,877 controls from Iceland. We identified a common sequence variant at 7q31 (rs4236601[A], odds ratio (OR) = 1.36, P = 5.0 Ă— 10?10). We then replicated the association in sample sets of 2,175 POAG cases and 2,064 controls from Sweden, the UK and Australia (combined OR = 1.18, P = 0.0015) and in 299 POAG cases and 580 unaffected controls from Hong Kong and Shantou, China (combined OR =5.42, P = 0.0021). The risk variant identified here is located close to CAV1 and CAV2, both of which are expressed in the trabecular meshwork and retinal ganglion cells that are involved in the pathogenesis of POAG
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