Abstract: Samples of precipitation and atmospheric water vapor were collected together with shallow firn/ice cores as part of the new deep drilling project in northwest Greenland: the NEEM project. These samples were analyzed for their isotope composition to understand the processes affecting the climatic signal archived in the water stable isotope records from the NEEM deep ice core. The dominant moisture source for the snow deposited at the NEEM-site may be originating as far south as 35N from the western part of the Atlantic Ocean. The surface atmospheric water vapor appears in isotopic equilibrium with the snow surface indicating a large water exchange between the atmosphere and snowpack. The interannual variability of NEEM shallow firn/ice cores stable isotope data covering the last ~40 years shows an unexpectedly weak NAO signal. Regional to global atmospheric models simulate a dominant summer precipitation in the NEEM area, suggesting that the intermittency of modern winter precipitation is responsible for the lack of a strong NAO imprint. The interannual variability of NEEM isotope data however shows a strong correlation with interannual variations of Baffin Bay sea ice cover, a relationship consistent with air mass trajectories. NEEM deep ice core isotopic records may therefore provide detailed information on past Baffin Bay sea ice extent. NEEM stable water isotope content increasing trend points to a local warming trend of ~3.0C over the last 40 years.

Abstract: Species flocks (SFs) fascinate evolutionary biologists who wonder whether such striking diversification can be driven by normal evolutionary processes. Multiple definitions of SFs have hindered the study of their origins. Previous studies identified a monophyletic taxon as a SF if it displays high speciosity in an area in which it is endemic (criterion 1), high ecological diversity among species (criterion 2), and if it dominates the habitat in terms of biomass (criterion 3); we used these criteria in our analyses. Our starting hypothesis is that normal evolutionary processes may provide a sufficient explanation for most SFs. We thus clearly separate each criterion and identify which biological (intrinsic) and environmental (extrinsic) traits are most favourable to their realization. The first part focuses on evolutionary processes. We highlight that some popular putative causes of SFs, such as key innovations or ecological speciation, are neither necessary nor sufficient to fulfill some or all of the three criteria. Initial differentiation mechanisms are diverse and difficult to identify a posteriori because a primary differentiation of one type (genetic, ecological or geographical) often promotes other types of differentiation. Furthermore, the criteria are not independent: positive feedbacks between speciosity and ecological diversity among species are expected whatever the initial cause of differentiation, and ecological diversity should enhance habitat dominance at the clade level. We then identify intrinsic and extrinsic factors that favour each criterion. Low dispersal emerges as a convincing driver of speciosity. Except for a genomic architecture favouring ecological speciation, for which assessment is difficult, high effective population sizes are the single intrinsic factor that directly enhances speciosity, ecological diversity and habitat dominance. No extrinsic factor appeared to enhance all criteria simultaneously but a combination of factors (insularity, fragmentation and environmental stability) may favour the three criteria, although the effect is indirect for habitat dominance. We then apply this analytical framework to Antarctic marine environments by analysing data from 18 speciose clades belonging to echinoderms (five unrelated clades), notothenioid fishes (five clades) and peracarid crustaceans (eight clades). Antarctic shelf environments and history appear favourable to endemicity and speciosity, but not to ecological specialization. Two main patterns are distinguished among taxa. (i) In echinoderms, many brooding, species?rich and endemic clades are reported, but without remarkable ecological diversity or habitat dominance. In these taxa, loss of the larval stage is probably a consequence of past Antarctic environmental factors, and brooding is suggested to be responsible for enhanced allopatric speciation (via dispersal limitation). (ii) In notothenioids and peracarids, many clades fulfill all three SF criteria. This could result from unusual features in fish and crustaceans: chromosome instability and key innovations (antifreeze proteins) in notothenioids, ecological opportunity in peracarids, and a genomic architecture favouring ecological speciation in both groups. Therefore, the data do not support our starting point that normal evolutionary factors or processes drive SFs because in these two groups uncommon intrinsic features or ecological opportunity provide the best explanation. The utility of the three?criterion SF concept is therefore questioned and guidelines are given for future studies.

Abstract: EGU General Assembly 2015, Vienna, Austria, 2015
in: EGU2015-14472-1

Abstract: Investigating ecological relationships between predators and their environment is essential to understand the response of marine ecosystems to climate variability and change. This is particularly true in polar regions, where sea ice (a sensitive climate variable) plays a crucial yet highly dynamic and variable role in how it influences the whole marine ecosystem, from phytoplankton to top predators. For mesopredators such as seals, sea ice both supports a rich (under-ice) food resource, access to which depends on local to regional coverage and conditions. Here, we investigate sex-specific relationships between the foraging strategies of southern elephant seals (Mirounga leonina) in winter and spatio-temporal variability in sea ice concentration (SIC) and coverage in East Antarctica. We satellite-tracked 46 individuals undertaking post-moult trips in winter from Kerguelen Islands to the peri-Antarctic shelf between 2004 and 2014. These data indicate distinct general patterns of sea ice usage: while females tended to follow the sea ice edge as it extended northward, the males remained on the continental shelf despite increasing sea ice. Seal hunting time, a proxy of foraging activity inferred from the diving behaviour, was longer for females in late autumn in the outer part of the pack ice, ∼150–370km south of the ice edge. Within persistent regions of compact sea ice, females had a longer foraging activity (i) in the highest sea ice concentration at their position, but (ii) their foraging activity was longer when there were more patches of low concentration sea ice around their position (either in time or in space; 30days & 50km). The high spatio-temporal variability of sea ice around female positions is probably a key factor allowing them to exploit these concentrated patches. Despite lack of information on prey availability, females may exploit mesopelagic finfishes and squids that concentrate near the ice-water interface or within the water column (from diurnal vertical migration) in the pack ice region, likely attracted by an ice algal autumn bloom that sustains an under-ice ecosystem. In contrast, male foraging effort increased when they remained deep within the sea ice (420–960km from the ice edge) over the shelf. Males had a longer foraging activity (i) in the lowest sea ice concentration at their position, and (ii) when there were more patches of low concentration sea ice around their position (either in time or in space; 30days & 50km) presumably in polynyas or flaw leads between land fast and pack ice. This provides access to zones of enhanced resources in autumn or in early spring such as polynyas, the Antarctic shelf and slope. Our results suggest that some seals utilized a highly sea ice covered environment, which is key for their foraging effort, sustaining or concentrating resources during winter.

Abstract: W6. FSA 99-51