Transcontinental migratory connectivity predicts parasite prevalence in breeding populations of the European barn swallow. (26th February 2015)
- Record Type:
- Journal Article
- Title:
- Transcontinental migratory connectivity predicts parasite prevalence in breeding populations of the European barn swallow. (26th February 2015)
- Main Title:
- Transcontinental migratory connectivity predicts parasite prevalence in breeding populations of the European barn swallow
- Authors:
- von Rönn, J. A. C.
Harrod, C.
Bensch, S.
Wolf, J. B. W. - Abstract:
- <abstract abstract-type="main" id="jeb12585-abs-0001"> <title>Abstract</title> <p>Parasites exert a major impact on the eco‐evolutionary dynamics of their hosts and the associated biotic environment. Migration constitutes an effective means for long‐distance invasions of vector‐borne parasites and promotes their rapid spread. Yet, ecological and spatial information on population‐specific host–parasite connectivity is essentially lacking. Here, we address this question in a system consisting of a transcontinental migrant species, the European barn swallow (<italic>Hirundo rustica</italic>) which serves as a vector for avian endoparasites in the genera <italic>Plasmodium</italic>, <italic> Haemoproteus</italic> and <italic>Leucocytozoon</italic>. Using feather stable isotope ratios as geographically informative markers, we first assessed migratory connectivity in the host: Northern European breeding populations predominantly overwintered in dry, savannah‐like habitats in Southern Africa, whereas Southern European populations were associated with wetland habitats in Western Central Africa. Wintering areas of swallows breeding in Central Europe indicated a migratory divide with both migratory programmes occurring within the same breeding population. Subsequent genetic screens of parasites in the breeding populations revealed a link between the host's migratory programme and its parasitic repertoire<italic>:</italic> controlling for effects of local breeding location, prevalence<abstract abstract-type="main" id="jeb12585-abs-0001"> <title>Abstract</title> <p>Parasites exert a major impact on the eco‐evolutionary dynamics of their hosts and the associated biotic environment. Migration constitutes an effective means for long‐distance invasions of vector‐borne parasites and promotes their rapid spread. Yet, ecological and spatial information on population‐specific host–parasite connectivity is essentially lacking. Here, we address this question in a system consisting of a transcontinental migrant species, the European barn swallow (<italic>Hirundo rustica</italic>) which serves as a vector for avian endoparasites in the genera <italic>Plasmodium</italic>, <italic> Haemoproteus</italic> and <italic>Leucocytozoon</italic>. Using feather stable isotope ratios as geographically informative markers, we first assessed migratory connectivity in the host: Northern European breeding populations predominantly overwintered in dry, savannah‐like habitats in Southern Africa, whereas Southern European populations were associated with wetland habitats in Western Central Africa. Wintering areas of swallows breeding in Central Europe indicated a migratory divide with both migratory programmes occurring within the same breeding population. Subsequent genetic screens of parasites in the breeding populations revealed a link between the host's migratory programme and its parasitic repertoire<italic>:</italic> controlling for effects of local breeding location, prevalence of Africa‐transmitted <italic>Plasmodium</italic> lineages was significantly higher in individuals overwintering in the moist habitats of Western Central Africa, even among sympatrically breeding individuals with different overwintering locations. For the rarer <italic>Haemoproteus</italic> parasites, prevalence was best explained by breeding location alone, whereas no clear pattern emerged for the least abundant parasite <italic>Leucocytozoon</italic>. These results have implications for our understanding of spatio‐temporal host–parasite dynamics in migratory species and the spread of avian borne diseases.</p> </abstract> … (more)
- Is Part Of:
- Journal of evolutionary biology. Volume 28:Number 3(2015:Mar.)
- Journal:
- Journal of evolutionary biology
- Issue:
- Volume 28:Number 3(2015:Mar.)
- Issue Display:
- Volume 28, Issue 3 (2015)
- Year:
- 2015
- Volume:
- 28
- Issue:
- 3
- Issue Sort Value:
- 2015-0028-0003-0000
- Page Start:
- 535
- Page End:
- 546
- Publication Date:
- 2015-02-26
- Subjects:
- Evolution (Biology) -- Periodicals
Biology -- Periodicals
576.8 - Journal URLs:
- http://onlinelibrary.wiley.com/journal/10.1111/(ISSN)1420-9101 ↗
http://www.blackwell-synergy.com/member/institutions/issuelist.asp?journal=jeb ↗
http://onlinelibrary.wiley.com/ ↗
http://firstsearch.oclc.org ↗
http://firstsearch.oclc.org/journal=1010-061x;screen=info;ECOIP ↗ - DOI:
- 10.1111/jeb.12585 ↗
- Languages:
- English
- ISSNs:
- 1010-061X
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 4979.642100
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British Library HMNTS - ELD Digital store - Ingest File:
- 4194.xml