No abstract

. Diseaselimited distributions? Contrasts in the prevalence of avian malaria in shorebird species using marine and freshwater habitats. Á/ Oikos 109: 396 Á/404.Migratory shorebirds show strong dichotomies in habitat choice during both the breeding and nonbreeding season. Whereas High Arctic breeding species are restricted to coastal marine and saline habitats during the nonbreeding season, more southerly breeding species tend to use freshwater habitats away from coasts. It has been proposed that this co-variation in habitat use is a consequence of a single axis of adaptation to pathogens and parasites, which are hypothesized to be relatively scarce in High Arctic, marine, and saline habitats and relatively common at lower latitudes and in freshwater habitats. Here we examine this contrast by comparing the prevalence of avian malaria infections in shorebirds occupying different habitats. We used a PCR-based assay on 1319 individuals from 31 shorebird species sampled in the Arctic, in temperate Europe and in inland and marine habitats in West Africa. Infections mainly occurred in tropical wetlands, with the shorebirds in freshwater inland habitats having significantly higher prevalence of malaria than birds in marine coastal habitats. Infections were not found in birds migrating through Europe even though conspecifics did show infections in tropical Africa. Adults should resist infection better than juveniles, but showed higher malaria prevalence, suggesting that infection probability increases with cumulative exposure. We argue that exposure to vectors is the main factor explaining the habitat-related differences in malaria prevalence.

Summary 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 knot Calidris canutus shows 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.

There is a widespread concern about the direct and indirect effects of industrial fisheries; this concern is particularly pertinent for so-called “marine protected areas” (MPAs), which should be safeguarded by national and international law. The intertidal flats of the Dutch Wadden Sea are a State Nature Monument and are protected under the Ramsar convention and the European Union's Habitat and Birds Directives. Until 2004, the Dutch government granted permission for ~75% of the intertidal flats to be exploited by mechanical dredgers for edible cockles (Cerastoderma edule). Here we show that dredged areas belonged to the limited area of intertidal flats that were of sufficient quality for red knots (Calidris canutus islandica), a long-distance migrant molluscivore specialist, to feed. Dredging led to relatively lower settlement rates of cockles and also reduced their quality (ratio of flesh to shell). From 1998 to 2002, red knots increased gizzard mass to compensate for a gradual loss in shellfish quality, but this compensation was not sufficient and led to decreases in local survival. Therefore, the gradual destruction of the necessary intertidal resources explains both the loss of red knots from the Dutch Wadden Sea and the decline of the European wintering population. This study shows that MPAs that do not provide adequate protection from fishing may fail in their conservation objectives.