2017
DOI: 10.1007/s10336-017-1440-0
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Endogenous migratory behaviour in a diurnally migrating songbird

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Cited by 7 publications
(4 citation statements)
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“…Our finding of a February peak and a spring nadir in fat deposits is consistent with previous studies of American goldfinches in our study region in southeast MI (Dawson and Marsh, 1986), and with body composition analysis that found peak lipid content and body mass from December through February (Carey et al, 1978). These data support the importance of fat for small-bodied songbirds in winter and suggest that either migratory fueling is low in these diurnal partial migrants, as for other diurnal migrants (Bojarinova et al, 2008;Stey et al, 2017), or that our sample did not include enough active migrants to detect it.…”
Section: Discussionsupporting
confidence: 93%
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“…Our finding of a February peak and a spring nadir in fat deposits is consistent with previous studies of American goldfinches in our study region in southeast MI (Dawson and Marsh, 1986), and with body composition analysis that found peak lipid content and body mass from December through February (Carey et al, 1978). These data support the importance of fat for small-bodied songbirds in winter and suggest that either migratory fueling is low in these diurnal partial migrants, as for other diurnal migrants (Bojarinova et al, 2008;Stey et al, 2017), or that our sample did not include enough active migrants to detect it.…”
Section: Discussionsupporting
confidence: 93%
“…Given that many facultative migrants do not have consistent migratory routes and destinations across years, fattening may reflect insurance against uncertainty about refueling opportunities. In partial migrant systems, movements may be programmed and consistent, but only in particular populations [e.g., more northerly populations: Linnets (Linaria cannabina; Stey et al, 2017); goldcrests (Regulus regulus; Bojarinova et al, 2008) or subsets of populations (e.g., females and juveniles in European blackbirds (Turdus merula; Lundberg, 1985;Fudickar et al, 2013) and dark-eyed juncos (Junco hyemalis; Holberton, 1993)]. The migratory individuals in these populations show more fattening during the migratory season than do their resident counterparts (Lundberg, 1985;Jahn et al, 2010;Fudickar et al, 2013), but see Holberton (1993).…”
Section: Introductionmentioning
confidence: 99%
“…Moreover, such activity occurs at a species-and/or population-speci c time of the year and follows speci c circadian patterns (Schmaljohann et al 2015;Ilieva et al 2023). Most of our knowledge on temporal patterns of migratory activity between and within migratory seasons comes from experimental studies on small passerine birds that exclusively migrate either at night (reviewed in Berthold 1996;Gwinner 1996a;Gwinner 1996b) or during the daytime (Berthold 1996; Ramenofsky et al 2012; Bojarinova and Babushkina 2015; Stey et al 2017). Our knowledge of species that combine both diurnal and nocturnal movements is very scarce (Berthold 1978;Lundberg 1981; Watts et al 2016).…”
Section: Introductionmentioning
confidence: 99%
“…For example, captive birds exposed to constant light : dark cycles show migratory activity (i.e. ‘Zugunruhe’ or migratory restlessness) that coincides with known migration of their free-living conspecifics, indicating that migratory timing is innate [ 6 , 12 , 13 ]. However, the timing of ‘Zugunruhe’ in captive birds starts to drift without adjustments to photoperiod, highlighting the importance of light-input pathways for correcting such drift (reviewed in [ 14 , 15 ]).…”
Section: Introductionmentioning
confidence: 99%