Many hypotheses attempt to explain parasite–host associations, but rarely are they examined together in a single community. For hosts, key traits are the proportion of infected individuals (prevalence) and the diversity of parasites infecting them. A key parasite trait is host specificity, ranging from specialists infecting one or a few closely related species to generalists infecting many species. We tested 10 hypotheses to explain host‐parasite associations; five ‘host‐centric’ (e.g. prevalence is related to host abundance) and five ‘parasite‐centric’ (e.g. parasite abundance is related to host specificity). We analyzed a community of 67 locally transmitted avian haemosporidian parasite lineages (genera Plasmodium, Haemoproteus or Leucocytozoon), sampled from 2726 birds (64 species) in southern Sweden. Among host‐centric hypotheses, Haemoproteus and Leucocytozoon prevalence and Haemoproteus diversity were related to host habitat preferences, whereas there were no relationships with host abundance or body mass. Haemoproteus and Leucocytozoon prevalences were more similar among closely related than among distantly related host species. Haemoproteus prevalence and diversity were lower in host species with few close relatives (‘evolutionarily distinct’ hosts). Among parasite‐centric hypotheses, most lineages, even relative generalists, infected closely related host species more often than expected by chance. However, the host species of Haemoproteus and Leucocytozoon lineages overlapped less among lineages than expected by chance. Specialists did not reach higher prevalences than generalists on single host species. However, the abundance of Haemoproteus lineages was related to host specificity with generalists more common than specialists; this was driven by three closely related generalists. Host specificity of parasites was unrelated to the abundance or evolutionarily distinctiveness of their hosts. Parasite communities are likely structured by many factors and cannot be explained by hypotheses focusing solely on hosts or parasites. However, we found consistent effects of host phylogenetic relationships, plausibly a result of evolutionarily conserved host immune systems limiting parasite distributions.

Despite recent advances in technology, it remains difficult to connect breeding and non‐breeding areas of populations of migratory organisms due to the challenges of year‐round tracking. Here, we used the Eurasian reed warbler Acrocephalus scirpaceus, a passerine with a pronounced migratory divide to demonstrate the promise of integrating several sources of information within the Bayesian modelling framework for the study of migratory connectivity. To this end, we combined data from stable hydrogen isotope ratios (δ2H) of feathers, ring recoveries, and the geographic delineation of sub‐populations on either side of the migratory divide. Feather δ2H measurements from local juvenile birds sampled across the breeding range tightly correlated with amount‐weighted mean annual precipitation δ2H values predicted for the natal sites. Predicted natal origins of birds intercepted en route in the Mediterranean region largely differed among the five stopover sites. Thanks to the different migratory pathways used by different breeding populations and the existence of a migratory divide, we were able to effectively narrow the assigned regions of origin. Our results show that spatial resolution of likelihood‐based assignments of geographic origins based on δ2H measurements may improve significantly when prior probabilities derived from population‐specific migratory directions are included. Integrating information from stable isotopes, ring recoveries, geolocators and other sources within the Bayesian modelling framework will provide an extremely useful toolbox for the study of animal movements in the future.

Divergent selection and local adaptation are responsible for many phenotypic differences between populations, potentially leading to speciation through the evolution of reproductive barriers. Here we evaluated the morphometric divergence among west European populations of Reed Bunting in order to determine the extent of local adaptation relative to two important selection pressures often associated with speciation in birds: migration and diet. We show that, as expected by theory, migratory E. s. schoeniclus had longer and more pointed wings and a slightly smaller body mass than the resident subspecies, with the exception of E. s. lusitanica, which despite having rounder wings was the smallest of all subspecies. Tail length, however, did not vary according to the expectation (shorter tails in migrants) probably because it is strongly correlated with wing length and might take longer to evolve. E. s. witherbyi, which feed on insects hiding inside reed stems during the winter, had a very thick, stubby bill. In contrast, northern populations, which feed on seeds, had thinner bills. Despite being much smaller, the southern E. s. lusitanica had a significantly thicker, longer bill than migratory E. s. schoeniclus, whereas birds from the UK population had significantly shorter, thinner bills. Geometric morphometric analyses revealed that the southern subspecies have a more convex culmen than E. s. schoeniclus, and E. s. lusitanica differs from the nominate subspecies in bill shape to a greater extent than in linear bill measurements, especially in males. Birds with a more convex culmen are thought to exert a greater strength at the bill tip, which is in agreement with their feeding technique. Overall, the three subspecies occurring in Western Europe differ in a variety of traits following the patterns predicted from their migratory and foraging behaviours, strongly suggesting that these birds have became locally adapted through natural selection.

We describe the sequence and extent of the complex and little understood post‐juvenile and post‐breeding moults of Savi's Warblers Locustella luscinioides. In contrast to previous studies, the post‐juvenile moult occurred in at least 44% of the birds, 5% of which moulted some or all tertials and greater coverts. The timing of overlap between the filling and the post‐juvenile moults, and the fact that later‐moulting birds had no post‐juvenile moult, strongly suggests that the moult extent is dependent on fledging date. From July onwards, all adult males overlapped breeding and moult, whereas only 11% of the females did so. The start of moult varied from 6 June to 25 August, and was significantly earlier in males. Only 18% of the birds completed the moult, whereas the remaining individuals retained a variable number of inner primaries and/or secondaries. Interestingly, not only was the number of retained primaries positively associated with the date of moult, but so too was the primary number of birds in which the moult started. We view this as an adaptation allowing the replacement of the most important feathers for flight when the time available for moult is short. Body condition did not vary with the progress of moult when date was taken into account, but fat reserves still tended to decrease and then increase. The body condition was correlated positively with the wing raggedness, so Savi's Warblers do not compensate for an increasing wing load during moult.