J. I. 2004. Intraspecific variation in movement patterns: modeling individual behaviour in a large marine predator. Á/ Oikos 105: 15 Á/ 30.In large marine predators, foraging entails movement. Quantitative models reveal how behaviours can mediate individual movement, such that deviations from a random pattern may reveal specific search tactics or behaviour. Using locations for 52 grey seals fitted with satellite-linked recorders on Sable Island; we modeled movement as a correlated random walk (CRW) for individual animals, at two temporal scales. Mean move length, turning angle, and net squared displacement (R 2 n : the rate of change in area over time) at successive moves over 3 to 10 months were calculated. The distribution of move lengths of individual animals was compared to a Lévy distribution to determine if grey seals use a Lévy flight search tactic. Grey seals exhibited three types of movement as determined by CRW model fit: directed movers Á/ animals displaying directed long distance travel that were significantly underpredicted by the CRW (23% of animals); residents Á/ animals remaining in the area surrounding Sable Island that were overpredicted by the model (29% of animals); and correlated random walkers Á/ those (48% of animals) in which movement was predicted by the CRW model. Kernel home range size differed significantly among all three movement types, as did travel speed, mean move length, mean R 2 n and total distance traveled. Sex and season of deployment were significant predictors of movement type, with directed movers more likely to be male and residents more likely to be female. Only 30% of grey seals fit a Lévy distribution, which suggests that food patches used by the majority of seals are not randomly distributed. Intraspecific variation in movement behaviour is an important characteristic in grey seal foraging ecology, underscoring the need to account for such variability in developing models of habitat use and predation.Most animals must move to locate and capture food. Thus, patterns of movement are considered a key factor in the survival of most organisms (Turchin 1998, Bergman et al. 2000. In any given environment, there is a range of behaviours (i.e. phenotypes) that can be considered successful. These can be learned behaviours, or alternatively, the products of longer-term selection for specific traits (Komers 1997). Intraspecific variation in movement behaviour reflects the different tactics used by individuals or sexes within a species or population to meet the demands of survival. We expect natural selection to favour those strategies that maximize fitness or some proxy of fitness, such as the rate of resource acquisition, or production of offspring. Given that natural selection operates at the level of the individual, ecological models that lump all individuals into the same behavioural category effectively disregard this variation (Judson 1994, Zollner andLima 1999). Consequently, examining average responses across populations obscures variability in behavioural ecology. Animal...
Establishing where and when predators forage is essential to understanding trophic interactions, yet foraging behavior remains poorly understood in large marine carnivores. We investigated the factors leading to foraging success in gray seals (Halichoerus grypus) in the Northwest Atlantic in the first study to use simultaneous deployments of satellite transmitters, time depth recorders, and stomach-temperature loggers on a free-ranging marine mammal. Thirty-two seals were each fitted with the three types of instrumentation; however, complete records from all three instruments were obtained from only 13 individuals, underscoring the difficulty of such a multi-instrument approach. Our goal was to determine the characteristics of diving, habitat, and movement that predict feeding. We linked diving behavior to foraging success at two temporal scales: trips (days) and bouts (hours) to test models of optimal diving, which indicate that feeding can be predicted by time spent at the bottom of a dive. Using an information-theoretic approach, a Generalized Linear Mixed Model with trip duration and accumulated bottom time per day best explained the number of feeding events per trip, whereas the best predictor of the number of feeding events per bout was accumulated bottom time. We then tested whether characteristics of movement were predictive of feeding. Significant predictors of the number of feeding events per trip were angular variance (i.e., path tortuosity) and distance traveled per day. Finally, we integrated measures of diving, movement, and habitat at four temporal scales to determine overall predictors of feeding. At the 3-h scale, mean bottom time and distance traveled were the most important predictors of feeding frequency, whereas at the 6-h and 24-h time scales, distance traveled alone was most important. Bathymetry was the most significant predictor of feeding at the 12-h interval, with feeding more likely to occur at deeper depths. Our findings indicate that several factors predict feeding in gray seals, but predictor variables differ across temporal scales such that environmental variation becomes important at some scales and not others. Overall, our results illustrate the value of simultaneously recording and integrating multiple types of information to better understand the circumstances leading to foraging success.
Summary 1.We studied feeding frequency in free-ranging grey seals using stomach temperature telemetry to test if previously reported sex differences in the diving, movement and diet were reflected in the temporal pattern of foraging success. 2. Data were retrieved from 21 of 32 grey seals from 1999 to 2001, totalling 343 days and 555 feeding events, with individual record length varying from 2 to 40 days (mean: 16·33 ± 2·67 days/seal). 3. Seals fed on 57·8 ± 6·46% of days sampled and had an average of 1·7 ± 0·26 meals per day, but individual variability was apparent in the temporal distribution of feeding as evidenced by high coefficients of variation (coefficient of variation = 69·0%). 4. Bout analysis of non-feeding intervals of six grey seals suggests that feeding intervals of individuals were varied and probably reflect differences in prey availability. Grey seals tended to have many single feeding events with long periods separating each event, as would be expected for a large carnivore with a batch-reactor digestive system. 5. We found significant sex differences in the temporal distribution of feeding. The number of feeding events per day was greater in males (2·2 ± 0·4 vs. 1·0 ± 0·2), as was time associated with feeding per day (56·6 ± 5·8 min vs. 43·9 ± 9·4 min). 6. The number of feeding events varied with time of day with the least number occurring during dawn. Feeding event size differed significantly by time of day, with greater meal sizes during the dawn and the smallest meals during the night. 7. The length of time between meals increased with the size of the previous meal, and was significantly less in males (541·4 ± 63·5 min) than in females (1092·6 ± 169·9 min). 8. These results provide new insight into the basis of sex differences in diving and diet in this large size-dimorphic marine predator.
Several methods have been used to identify erroneous animal locations based on Argos satellite data. Using 15,987 satellite locations for 37 gray seals (Haliockoerus grypus), we tested a three‐stage filtering algorithm designed to address shortcomings of other filters. In stage 1, for each location, four rates of travel were calculated—the rate to each of the two previous locations and the two subsequent locations. If all four rates exceeded 2 m/sec (95th percentile of our data), the location was removed (7.25% of total locations). Stage 2 incorporated the filtering algorithm developed by McConnell et al. (1992) resulting in the rejection of 22.75% of total locations based on reasonable assumptions of straight‐line travel. At stage 3, the remaining data were evaluated against a distance threshold, defined as the 99th percentile of realized distance traveled over a period of seven days. Locations exceeding this threshold‐were rejected (0.69% of total locations). Overall, the three‐stage filter eliminated fewer locations (30.7 ± 1.62%), than the stage 2 filter alone. Most standard locations were retained, but 85.7% of location class 0, 76.6% of A, and 41.9% of B were also retained. These location classes account for most of data routinely collected but not used.
BackgroundAdverse childhood experiences (ACE) have been previously linked to quality of life, health conditions, and life expectancy in adulthood. Less is known about the potential mechanisms which mediate these associations. This study examined how ACE influences adult health-related quality of life (HRQoL) in a low-income community in Florida.MethodsA community-based participatory needs assessment was conducted from November 2013 to March 2014 with 201 residents of Tampa, Florida, USA. HRQoL was measured by an excessive number of unhealthy days experienced during the previous 30-day window. Mediation analyses for dichotomous outcomes were conducted with logistic regression. Bootstrapped confidence intervals were generated for both total and specific indirect effects.ResultsMost participants reported ‘good to excellent health’ (76 %) and about a fourth reported ‘fair to poor health’ (24 %). The mean of total unhealthy days was 9 days per month (SD ±10.5). Controlling for demographic and neighborhood covariates, excessive unhealthy days was associated with ACE (AOR = 1.23; 95 % CI: 1.06, 1.43), perceived stress (AOR = 1.07; 95 % CI: 1.03, 1.10), and sleep disturbance (AOR = 8.86; 3.61, 21.77). Mediated effects were significant for stress (β = 0.08) and sleep disturbances (β = 0.11) as they related to the relationship between ACE and excessive unhealthy days.ConclusionACE is linked to adult HRQoL. Stress and sleep disturbances may represent later consequences of childhood adversity that modulate adult quality of life.Electronic supplementary materialThe online version of this article (doi:10.1186/s12955-015-0323-4) contains supplementary material, which is available to authorized users.
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