Wild birds, in particular waterfowl, are common reservoirs of low pathogenic avian influenza viruses, and infected individuals could spread the viruses during migrations. We used satellite telemetry to track the spring migration of the mallard ducks ( Anas platyrhynchos ) that winter in Japan. We studied their migration routes, distribution of stopover and breeding sites, and timing of migration movements. We tracked 23 mallards from four different wintering sites. Nine of the 23 mallards reached presumable breeding sites, where migration terminated. The migration routes of the birds greatly differed not only among the wintering sites but also within the same wintering site, although the general feature of the routes was shared among birds within the same wintering site. The mallards used several stopover sites, and they typically stayed for a long period (about one to four weeks) at a site between migration intervals of two to three days. Stopover sites were located in northeast Japan, the eastern coastline of South Korea and North Korea, and the interior of Far Eastern Russia. Mallards from three different wintering sites used a stopover area near the middle part of the Ussuri river in Russia. The terminal sites, which were presumably also breeding sites, were distributed widely over northeast Asia and Far Eastern Russia. These results suggest that mallards that winter in Japan originate from breeding areas widely distributed across eastern Asia. Mallards could potentially transmit avian influenza viruses between Japan and a broad region of northeastern Asia.

Assortative mating is an important pre‐mating isolation mechanism that has been observed in some wild populations of seabirds. The Short‐tailed Albatross Phoebastria albatrus is a globally Vulnerable seabird that breeds mainly on Torishima and the Senkaku Islands in the north‐western Pacific Ocean. Our previous studies suggested that two genetically distinct populations exist, one on Torishima and the other on the Senkaku Islands. Recently, however, several un‐ringed birds in subadult plumage have been observed breeding on Torishima in the Hatsunezaki colony. As almost all birds hatched on Torishima since 1979 have been ringed, the natal site of the un‐ringed birds was suspected to be the Senkaku Islands. Genetic differences between the two populations would reveal the natal sites of un‐ringed birds. By observing the ring status (ringed or un‐ringed) of mating pairs and analysing the mitochondrial DNA (mtDNA) control region 2 of un‐ringed birds, we assessed whether birds that originated from Torishima and the Senkaku Islands achieved pre‐mating isolation. There was a small number of pairs on Torishima that consisted of one ringed and one un‐ringed bird, but the observed number was significantly lower than that expected if ringed and un‐ringed birds mated randomly. Furthermore, mtDNA analyses of nine un‐ringed birds demonstrated that all belonged to a particular haplotype clade from the Senkaku Islands. These results show that birds from Torishima and the Senkaku Islands mate assortatively but that there is incomplete pre‐mating isolation between birds from the two island groups. The pre‐mating isolation of these two populations of Short‐tailed Albatross could arise from differences in the timing of breeding and incompatibility in mating displays. As the divergence between the two populations is unlikely to be sufficient to achieve complete post‐mating isolation, the two groups are likely to be hybridizing. Further studies using molecular and/or behavioural analyses would be required to reveal the evolutionary significance of hybridization between these two populations.

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The occurrence of cryptic species within a threatened taxon is rare, but where they do occur, understanding species boundaries is essential for planning an effective conservation strategy. The short-tailed albatross Phoebastria albatrus is a Vulnerable seabird that mainly breeds on Torishima and the Senkaku Islands in the western North Pacific. Although it has been tacitly regarded as a single management unit with 2 breeding sites, the species is known to comprise 2 genetically separated populations (Senkaku-type and Torishima-type). However, morphological examination of birds from both populations has not been conducted owing to the difficulty in accessing the Senkaku Islands. In this study, we examined the morphological differences between immigrants from the Senkaku Islands to Torishima (Senkaku-type) and native birds on Torishima (Torishima-type) and found significant differences in morphological characteristics between the 2 bird types. In general, Torishima-type birds were larger than Senkaku-type birds, whereas Senkaku-type birds had relatively longer beaks. Based on the morphological differences found in this study as well as genetic and ecological differences revealed in previous studies, we believe that Senkaku- and Torishima-type birds should be classified as different cryptic species. To the best of our knowledge, this is the first case of cryptic species being identified in a threatened avian species.

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