Selection of diving strategy by Antarctic fur seals depends on where and when foraging takes place

We investigated the spatial and temporal distribution of foraging effort by lactating Antarctic fur seals Arctocephalus gazella at Heard Island using satellite telemetry and time-depth recorders. Two principal diving types were identified: ‘deep’ dives averaging 48.6 m, and ‘shallow’ dives averaging 8.6 m. Discriminant function analyses were used to assign dives based on their depth and duration. Generalised linear mixed-effects models of night dives (>80% of all dives) indicated both spatial and temporal effects on the distribution of deep and shallow dives. Deep dives were more common in the deeper shelf waters of the Kerguelen Plateau, and these dives predominantly occurred after sunset and before sunrise. In contrast, shallow dives were more common in slope waters on the southeastern margin of the Kerguelen Plateau in the hours either side of local midnight. We suggest that these 2 distinct diving types reflect the targeting of channichthyid (deep dives) and myctophid (shallow dives) fish, and are indicative of spatial and temporal differences in the availability of these 2 important prey groups. We also identified 3 distinct behavioural dive groups (based on multidimensional scaling of 19 diving and foraging trip parameters) that also differed in their spatial distribution and in their relative importance of deep and shallow dives. The present study provides some of the first evidence that diving strategies are not only influenced by where foraging takes pace, but also when.Simon D. Goldsworthy, Brad Page, Andrew Welling, Magaly Chambellant, Corey J. A. Bradsha

Toxoplasma gondii seroprevalence in ringed seals (Pusa hispida) from the Canadian Arctic

Toxoplasmosis is a significant public health threat for Inuit in the Canadian Arctic. This study aimed to investigate arctic seals as a possible food-borne source of infection. Blood samples collected from 828 seals in 7 Canadian Arctic communities from 1999 to 2006 were tested for Toxoplasma gondii antibodies using a direct agglutination test. Polymerase chain reaction (PCR) was used to detect T. gondii DNA in tissues of a subsample of seals. Associations between seal age, sex, species, diet, community and year of capture, and serological test results were investigated by logistic regression. Overall seroprevalence was 10.4% (86/828). All tissues tested were negative by PCR. In ringed seals, seroprevalence was significantly higher in juveniles than in adults (odds ratio = 2.44). Overall, seroprevalence varied amongst communities (P = 0.0119) and by capture year (P = 0.0001). Our study supports the hypothesis that consumption of raw seal meat is a significant source of infection for Inuit. This work raises many questions about the mechanism of transfer of this terrestrial parasite to the marine environment, the preponderance of infection in younger animals and the natural course of infection in seals. Further studies to address these questions are essential to fully understand the health risks for Inuit communities

Ringed seal demography in a changing climate

Climate change is affecting species’ distributions and abundances worldwide. Baseline population estimates, against which future observations may be compared, are necessary if we are to detect ecological change. Arctic sea ice ecosystems are changing rapidly and we lack baseline population estimates for many ice‐associated species. Provided we can detect them, changes in Arctic marine ecosystems may be signaled by changes in indicator species such as ringed seals (Pusa hispida). Ringed seal monitoring has provided estimates of survival and fertility rates, but these have not been used for population‐level inference. Using matrix population models, we synthesized existing demographic parameters to obtain estimates of historical ringed seal population growth and structure in Amundsen Gulf and Prince Albert Sound, Canada. We then formalized existing hypotheses about the effects of emerging environmental stressors (i.e., earlier spring ice breakup and reduced snow depth) on ringed seal pup survival. Coupling the demographic model to ice and snow forecasts available from the Coupled Model Intercomparison Project resulted in projections of ringed seal population size and structure up to the year 2100. These projections showed median declines in population size ranging from 50% to 99%. Corresponding to these projected declines were substantial changes in population structure, with increasing proportions of ringed seal pups and adults and declining proportions of juveniles. We explored if currently collected, harvest‐based data could be used to detect the projected changes in population stage structure. Our model suggests that at a present sample size of 100 seals per year, the projected changes in stage structure would only be reliably detected by mid‐century, even for the most extreme climate models. This modeling process revealed inconsistencies in existing estimates of ringed seal demographic rates. Mathematical population models such as these can contribute both to understanding past population trends as well as predicting future ones, both of which are necessary if we are to detect and interpret future observations

Mama's boy: sex differences in juvenile survival in a highly dimorphic large mammal, the Galapagos sea lion

Kraus C, Mueller B, Meise K, Piedrahita P, Pörschmann U, Trillmich F. Mama's boy: sex differences in juvenile survival in a highly dimorphic large mammal, the Galapagos sea lion. Oecologia. 2013;171(4):893-903.In many mammals, early survival differs between the sexes, with males proving the more fragile sex ["Fragile male (FM) hypothesis"], especially in sexually dimorphic species where males are the larger sex. Male-biased allocation (MBA) by females may offset this difference. Here, we evaluate support for the FM and MBA hypotheses using a dataset on Galapagos sea lions (Zalophus wollebaeki). We statistically model sex-specific survival as it depends on body mass and environmental conditions (sea surface temperature, SST, a correlate of marine productivity) at three developmental stages, the perinatal phase (1st month), the main lactation period (1st year), and the weaning period (2nd year). Supporting the FM hypothesis, we found that, early in life (1st month), at equal birth mass, males survived less well than females. During the remainder of the first year of life, male survival was actually less sensitive to harsh environmental conditions than that of females, contradicting the FM hypothesis and supporting the MBA hypothesis. During the second year of life, only male survival suffered with high SSTs as predicted by the FM hypothesis. At each developmental stage, observed survival rates were almost equal for both sexes, suggesting that mothers buffer against the inherent fragility of male offspring through increased allocation, thereby masking the differences in survival prospects between the sexes