Please use this identifier to cite or link to this item: http://dr.iiserpune.ac.in:8080/xmlui/handle/123456789/4022
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dc.contributor.authorTUNG, SUDIPTAen_US
dc.contributor.authorMishra, Abhisheken_US
dc.contributor.authorShreenidhi, P. M.en_US
dc.contributor.authorSadiq, Mohammed Aamiren_US
dc.contributor.authorJOSHI, SRIPADen_US
dc.contributor.authorSHREE SRUTI, V. R.en_US
dc.contributor.authorDEY, SUTIRTHen_US
dc.date.accessioned2019-09-09T11:38:48Z
dc.date.available2019-09-09T11:38:48Z
dc.date.issued2018-01en_US
dc.identifier.citationOIKOS, 127(1), 34-44.en_US
dc.identifier.issn0030-1299en_US
dc.identifier.issn1600-0706en_US
dc.identifier.urihttp://dr.iiserpune.ac.in:8080/xmlui/handle/123456789/4022
dc.identifier.urihttps://doi.org/10.1111/oik.04618en_US
dc.description.abstractGlobal climate is changing rapidly and is accompanied by large‐scale fragmentation and destruction of habitats. Since dispersal is the first line of defense for mobile organisms to cope with such adversities in their environment, it is important to understand the causes and consequences of evolution of dispersal. Although dispersal is a complex phenomenon involving multiple dispersal‐components like propensity (tendency to leave the natal patch) and ability (to travel long distances), the relationship between these traits is not always straight‐forward, it is not clear whether these traits can evolve simultaneously or not, and how their interactions affect the overall dispersal profile. To investigate these issues, we subjected four large (n ∼ 2400) outbred populations of Drosophila melanogaster to artificial selection for increased dispersal, in a setup that mimicked increasing habitat fragmentation over 33 generations. The propensity and ability of the selected populations were significantly greater than the non‐selected controls and the difference persisted even in the absence of proximate drivers for dispersal. The dispersal kernel evolved to have significantly greater standard deviation and reduced values of skew and kurtosis, which ultimately translated into the evolution of a greater frequency of long‐distance dispersers (LDDs). We also found that although sex‐biased dispersal exists in D. melanogaster, its expression can vary depending on which dispersal component is being measured and the environmental condition under which dispersal takes place. Interestingly though, there was no difference between the two sexes in terms of dispersal evolution. We discuss possible reasons for why some of our results do not agree with previous laboratory and field studies. The rapid evolution of multiple components of dispersal and the kernel, expressed even in the absence of stress, indicates that dispersal evolution cannot be ignored while investigating eco‐evolutionary phenomena like speed of range expansion, disease spread, evolution of invasive species and destabilization of metapopulation dynamics.en_US
dc.language.isoenen_US
dc.publisherWileyen_US
dc.subjectSimultaneous evolutionen_US
dc.subjectMultiple Dispersalen_US
dc.subjectComponents kernelen_US
dc.subjectGlobal climateen_US
dc.subject2018en_US
dc.titleSimultaneous evolution of multiple dispersal components and kernelen_US
dc.typeArticleen_US
dc.contributor.departmentDept. of Biologyen_US
dc.identifier.sourcetitleOIKOSen_US
dc.publication.originofpublisherForeignen_US
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