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Longitudinal tracking studies have revealed consistent differences in the migration patterns of individuals from the same populations. The sources or processes causing this individual variation are largely unresolved. As a result, it is mostly unknown how much, how fast and when animals can adjust their migrations to changing environments.We studied the ontogeny of migration in a long‐distance migratory shorebird, the black‐tailed godwit Limosa limosa limosa, a species known to exhibit marked individuality in the migratory routines of adults. By observing how and when these individual differences arise, we aimed to elucidate whether individual differences in migratory behaviour are inherited or emerge as a result of developmental plasticity.We simultaneously tracked juvenile and adult godwits from the same breeding area on their south‐ and northward migrations. To determine how and when individual differences begin to arise, we related juvenile migration routes, timing and mortality rates to hatch date and hatch year. Then, we compared adult and juvenile migration patterns to identify potential age‐dependent differences.In juveniles, the timing of their first southward departure was related to hatch date. However, their subsequent migration routes, orientation, destination, migratory duration and likelihood of mortality were unrelated to the year or timing of migration, or their sex. Juveniles left the Netherlands after all tracked adults. They then flew non‐stop to West Africa more often and incurred higher mortality rates than adults. Some juveniles also took routes and visited stopover sites far outside the well‐documented adult migratory corridor. Such juveniles, however, were not more likely to die.We found that juveniles exhibited different migratory patterns than adults, but no evidence that these behaviours are under natural selection. We thus eliminate the possibility that the individual differences observed among adult godwits are present at hatch or during their first migration. This adds to the mounting evidence that animals possess the developmental plasticity to change their migration later in life in response to environmental conditions as those conditions are experienced. [ABSTRACT FROM AUTHOR]

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Evolutionary theories of seasonal migration generally assume that the costs of longer migrations are balanced by benefits at the non‐breeding destinations.We tested, and rejected, the null hypothesis of equal survival and timing of spring migration for High Arctic breeding sanderling Calidris alba using six and eight winter destinations between 55°N and 25°S, respectively.Annual apparent survival was considerably lower for adult birds wintering in tropical West Africa (Mauritania: 0.74 and Ghana: 0.75) than in three European sites (0.84, 0.84 and 0.87) and in subtropical Namibia (0.85). Moreover, compared with adults, second calendar‐year sanderlings in the tropics, but not in Europe, often refrained from migrating north during the first possible breeding season. During northward migration, tropical‐wintering sanderlings occurred at their final staging site in Iceland 5–15 days later than birds wintering further north or south. Namibia‐wintering sanderlings tracked with solar geolocators only staged in West Africa during southward migration.The low annual survival, the later age of first northward migration and the later passage through Iceland during northward migration of tropical‐wintering sanderlings, in addition to the skipping of this area during northward but not southward migration by Namibia‐wintering sanderlings, all suggest they face issues during the late non‐breeding season in West Africa.Migrating sanderlings defy long distances but may end up in winter areas with poor fitness prospects. We suggest that ecological conditions in tropical West Africa make the fuelling prior to northward departure problematic. [ABSTRACT FROM AUTHOR]

Models relating intake rate to food abundance and competitor density (generalized functional response models) can predict forager distributions and movements between patches, but we lack understanding of how distributions and small-scale movements by the foragers themselves affect intake rates., Using a state-of-the-art approach based on continuous-time Markov chain dynamics, we add realism to classic functional response models by acknowledging that the chances to encounter food and competitors are influenced by movement decisions, and, vice versa, that movement decisions are influenced by these encounters., We used a multi-state modelling framework to construct a stochastic functional response model in which foragers alternate between three behavioural states: searching, handling and moving., Using behavioural observations on a molluscivore migrant shorebird (red knot, Calidris canutus canutus), at its main wintering area (Banc d'Arguin, Mauritania), we estimated transition rates between foraging states as a function of conspecific densities and densities of the two main bivalve prey., Intake rate decreased with conspecific density. This interference effect was not due to decreased searching efficiency, but resulted from time lost to avoidance movements., Red knots showed a strong functional response to one prey ( Dosinia isocardia), but a weak response to the other prey ( Loripes lucinalis). This corroborates predictions from a recently developed optimal diet model that accounts for the mildly toxic effects due to consuming Loripes., Using model averaging across the most plausible multi-state models, the fully parameterized functional response model was then used to predict intake rate for an independent data set on habitat choice by red knot., Comparison of the sites selected by red knots with random sampling sites showed that the birds fed at sites with higher than average Loripes and Dosinia densities, that is sites for which we predicted higher than average intake rates., We discuss the limitations of Holling's classic functional response model which ignores movement and the limitations of contemporary movement ecological theory that ignores consumer-resource interactions. With the rapid advancement of technologies to track movements of individual foragers at fine spatial scales, the time is ripe to integrate descriptive tracking studies with stochastic movement-based functional response models. [ABSTRACT FROM AUTHOR]

1. When prey occur at high densities, energy assimilation rates are generally constrained by rates of digestion rather than by rates of collection (i.e. search and handle). As predators usually select patches containing high prey densities, rates of digestion will play an important role in the foraging ecology of a species.2. The red knotCalidris canutusshows tremendous inter- and intra-individual variation in maximum rates of digestion due to variation in the size of the processing machinery (gizzard and intestine), which makes it a suitable species to study the effects of digestive processing rate on foraging decisions.3. Here we report on patch use, prey choice, and daily foraging times as a function of gizzard size in free-ranging, radio-marked, red knots. As knots crush their bulky bivalve prey in their gizzard, the size of this organ, which we measured using ultrasonography, determines digestive processing rate.4. Using the digestive rate model, we a priori modelled patch use, prey choice, and daily foraging times as a function of gizzard mass. Focusing on two contrasting patches, birds with small gizzards were expected to feed on high-quality (soft-bodied) prey found in low densities in the one patch, while birds with large gizzards were expected to feed on low-quality (hard-shelled) prey found in high densities in the other patch. Assuming that red knots aim to balance their energy budget on a daily basis, we expected daily foraging time to decline with gizzard mass.5. Observed patch and prey choices were in quantitative agreement with these theoretical predictions. Observed daily foraging times were only in qualitative agreement: they declined with gizzard mass but less steeply than predicted.6. We discuss that red knots might be aiming for a slightly positive energy budget in order to (i) refuel their stores depleted during migration, and (ii) to insure against unpredictability in supply and demand during winter. Red knots arriving from their breeding grounds with small gizzards are only able to realize this aim when densities of soft-bodied prey are high, which is the case in late July and early August. Rapidly declining soft-bodied prey densities throughout late summer pose a major penalty for individuals arriving late at their wintering grounds.7. The long daily foraging periods required by knots with small gizzards are only feasible through‘tide-extension’. In our study area, birds can and do raise the daily low tide period from 12 h to almost 17 h by moving along with the tide in an easterly direction, subsequently flying back to their starting point at the high tide roost.Journal of Animal Ecology(2005) doi: 10.1111/j.1365-2656.2004.00904.x [ABSTRACT FROM AUTHOR]