BackgroundSpace use strategies by foraging animals are often considered to be species-specific. However, similarity between conspecific strategies may also result from similar resource environments. Here, we revisit classic predictions of the relationships between the resource distribution and foragers’ space use by tracking free-living foragers of a single species in two contrasting resource landscapes. At two main non-breeding areas along the East-Atlantic flyway (Wadden Sea, The Netherlands and Banc d’Arguin, Mauritania), we mapped prey distributions and derived resource landscapes in terms of the predicted intake rate of red knots (Calidris canutus), migratory molluscivore shorebirds. We tracked the foraging paths of 13 and 38 individual red knots at intervals of 1 s over two and five weeks in the Wadden Sea and at Banc d’Arguin, respectively. Mediated by competition for resources, we expected aggregation to be strong and site fidelity weak in an environment with large resource patches. The opposite was expected for small resource patches, but only if local resource abundances were high.ResultsCompared with Banc d’Arguin, resource patches in the Wadden Sea were larger and the maximum local resource abundance was higher. However, because of constraints set by digestive capacity, the average potential intake rates by red knots were similar at the two study sites. Space-use patterns differed as predicted from these differences in resource landscapes. Whereas foraging red knots in the Wadden Sea roamed the mudflats in high aggregation without site fidelity (i.e. grouping nomads), at Banc d’Arguin they showed less aggregation but were strongly site-faithful (i.e. solitary residents).ConclusionThe space use pattern of red knots in the two study areas showed diametrically opposite patterns. These differences could be explained from the distribution of resources in the two areas. Our findings imply that intraspecific similarities in space use patterns represent responses to similar resource environments rather than species-specificity. To predict how environmental change affects space use, we need to understand the degree to which space-use strategies result from developmental plasticity and behavioural flexibility. This requires not only tracking foragers throughout their development, but also tracking their environment in sufficient spatial and temporal detail.Electronic supplementary materialThe online version of this article (10.1186/s40462-018-0142-4) contains supplementary material, which is available to authorized users.
The wealth of field studies using stable isotopes to make inferences about animal diets require controlled validation experiments to make proper interpretations. Despite several pleas in the literature for such experiments, validation studies are still lagging behind, notably in consumers dwelling in chemosynthesis-based ecosystems. In this paper we present such a validation experiment for the incorporation of 13C and 15N in the blood plasma of a medium-sized shorebird, the red knot (Calidris canutus canutus), consuming a chemosymbiotic lucinid bivalve (Loripes lucinalis). Because this bivalve forms a symbiosis with chemoautotrophic sulphide-oxidizing bacteria living inside its gill, the bivalve is isotopically distinct from ‘normal’ bivalves whose food has a photosynthetic basis. Here we experimentally tested the hypothesis that isotope discrimination and incorporation dynamics are different when consuming such chemosynthesis-based prey. The experiment showed that neither the isotopic discrimination factor, nor isotopic turnover time, differed between birds consuming the chemosymbiotic lucinid and a control group consuming a photosynthesis-based bivalve. This was true for 13C as well as for 15N. However, in both groups the 15N discrimination factor was much higher than expected, which probably had to do with the birds losing body mass over the course of the experiment.
In the original publication of this article [1], the majority of the authors' proof corrections weren't processed due to a typesetting mistake. The original publication of this article has been updated to correct the missed corrections. An overview of the corrections can be found in Additional file 1. The publisher apologises to the readers and authors for the inconvenience.
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