2019
DOI: 10.1111/ibi.12752
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Range‐wide migration corridors and non‐breeding areas of a northward expanding Afro‐Palaearctic migrant, the European Bee‐eater Merops apiaster

Abstract: Across their ranges, different populations of migratory species often use separate routes to migrate between breeding and non‐breeding grounds. Recent changes in climate and land‐use have led to breeding range expansions in many species but it is unclear whether these populations also establish new migratory routes, non‐breeding sites and migration phenology. Thus, we compared the migration patterns of European Bee‐eaters Merops apiaster from two established western (n = 5) and eastern (n = 6) breeding populat… Show more

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Cited by 14 publications
(7 citation statements)
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“…In contrast, the early passage of the European bee-eater we uncovered herein is surprising as it is known to begin southward migration in mid-August, with a peak in September (Cramp, 1998). However, our findings do corroborate records from South Sinai, Egypt (Arcilla et al, 2016), and a study showing that distinct geographic populations of European bee-eater may differ in their migratory phenology by 2-4 weeks (Hahn et al, 2020).…”
Section: Phenologysupporting
confidence: 92%
“…In contrast, the early passage of the European bee-eater we uncovered herein is surprising as it is known to begin southward migration in mid-August, with a peak in September (Cramp, 1998). However, our findings do corroborate records from South Sinai, Egypt (Arcilla et al, 2016), and a study showing that distinct geographic populations of European bee-eater may differ in their migratory phenology by 2-4 weeks (Hahn et al, 2020).…”
Section: Phenologysupporting
confidence: 92%
“…These southern European breeding sites might have been colonized by individuals with Turkish origin, while breeding areas further north, were likely colonized from the east by individuals with Russian origin (Bozhko, 1980). Thus, the population specific routes and the migratory divide between the Bulgarian and more northern populations may also reflect historic species colonization routes (Hahn et al, 2019). The larger northward detour of the Czech birds that cannot be explained by optimal routes might still be a remnant of historic routes and not yet adapted to the local conditions.…”
Section: Discussionmentioning
confidence: 99%
“…However, in Palearctic species with intercontinental flyways to both Africa and Asia it is usually the case that individuals occupying the western part of the range take the western flyway and those in the eastern part of the breeding range migrate take the eastern flyway, with a clear migratory divide in the breeding range. This pattern has been demonstrated in, for example, Asian Houbara Bustard Chlamydotis macqueenii (Combreau et al 2011), a number of tundrabreeding species of the high Arctic (Alerstam & Gudmundsson 1999), European Bee-eater Merops apiaster (Hahn et al 2020) and many European-breeding passerines (Møller et al 2011). Red-necked Phalaropes Phalaropus lobatus in the western part of the European breeding range migrate westwards to the east Pacific and those in the eastern part of the European breeding range migrate south to the seas off Arabia and East Africa (van Bemmelen et al 2019).…”
Section: Discussionmentioning
confidence: 83%