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- Hjernquist, Marten B., et al.
(författare)
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High individual repeatability and population differentiation in stable isotope ratios in winter-grown collared flycatcher Ficedula albicollis feathers
- 2009
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Ingår i: Journal of Avian Biology. - 0908-8857 .- 1600-048X. ; 40:2, s. 102-107
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Tidskriftsartikel (refereegranskat)abstract
- For migrants, we often lack complete information of their spatial distribution year round. Here, we used stable carbon, nitrogen and hydrogen isotope ratios extracted from feathers grown at the wintering sites of the long-distance migratory collared flycatcher Ficedula albicollis, to study how individuals from different breeding populations are distributed at the wintering sites. A sub-sample of birds was also sampled in two consecutive years to test for the repeatability of isotope ratios. Birds from the same breeding populations had more similar isotope ratios compared to birds from other nearby populations (10-100 km apart). Furthermore, isotope repeatability within individuals was high, implying that the observed pattern of isotope variation is consistent between years. We put forward two hypotheses for these patterns; 1) strong wintering site philopatry and migratory connectivity, suggesting that migratory connectivity may potentially be found on a much smaller spatial scale than previously considered, and 2) consistent interpopulation differentiation of feeding ecology at their wintering site.
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- Klaassen, Marcel, et al.
(författare)
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Departure fuel loads in time-minimizing migrating birds can be explained by the energy costs of being heavy
- 1996
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Ingår i: Journal of Theoretical Biology. - : Elsevier BV. - 1095-8541 .- 0022-5193. ; 183:1, s. 29-34
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Tidskriftsartikel (refereegranskat)abstract
- Lindström & Alerstam (1992Am. Nat.140,477–491) presented a model that predicts optimal departure fuel loads as a function of the rate of fuel deposition in time-minimizing migrants. The basis of the model is that the coverable distance per unit of fuel deposited, diminishes with increasing fuel load. This is an effect of the increasing flight costs associated with increasing body mass. Lindström & Alerstam (1992) found that birds left at lower fuel loads than their model predicted for which they considered various ecological explanations. Alternatively, we hypothesize that the difference between prediction and empirical data might be a result of extra resting metabolic and transport costs associated with an increase in fuel load during stopover. We develop a new version of the Lindström & Alerstam (1992) model taking fuel load associated costs during stopover into account. We fit empirical data from rufous hummingbirdsSelasphorus rufus(Carpenteret al., 1983Proc. Natl. Acad. Sci. U.S.A.80,7259–7263) and bluethroatsLuscinia svecica(Lindström & Alerstam, 1992) to this new model. Estimated fuel-load costs are discussed in relation to knowledge presently available on variations in basal metabolic costs and transport costs with body mass. We show that fuel-load costs within a reasonable range can explain the observed departure fuel loads when migrating birds are time minimizers.
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- Lindström, Åke, et al.
(författare)
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A Puzzling Migratory Detour: Are Fueling Conditions In Alaska Driving The Movement Of Juvenile Sharp-Tailed Sandpipers?
- 2011
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Ingår i: The Condor: ornithological applications. - : Oxford University Press (OUP). - 0010-5422. ; 113:1, s. 129-139
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Tidskriftsartikel (refereegranskat)abstract
- Making a detour can be advantageous to a migrating bird if fuel-deposition rates at stopover sites along the detour are considerably higher than at stopover sites along a more direct route. One example of an extensive migratory detour is that of the Sharp-tailed Sandpiper (Calidris acuminata), of which large numbers of juveniles are found during fall migration in western Alaska. These birds take a detour of 1500-3400 km from the most direct route between their natal range in northeastern Siberia and nonbreeding areas in Australia. We studied the autumnal fueling rates and fuel loads of 357 Sharp-tailed Sandpipers captured in western Alaska. In early September the birds increased in mass at a rate of only 0.5% of lean body mass day(-1). Later in September, the rate of mass increase was about 6% of lean body mass day(-1), among the highest values found among similar-sized shorebirds around the world. Some individuals more than doubled their body mass because of fuel deposition, allowing non-stop flight of between 7100 and 9800 km, presumably including a trans-oceanic flight to the southern hemisphere. Our observations indicated that predator attacks were rare in our study area, adding another potential benefit of the detour. We conclude that the most likely reason for the Alaskan detour is that it allows juvenile Sharp-tailed Sand-pipers to put on large fuel stores at exceptionally high rates.
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- Lindström, Åke, et al.
(författare)
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Movement and migration in a changing world
- 2014
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Ingår i: Animal movement across scales. - : Oxford University Press. - 9780191785696 ; , s. 36-50
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Bokkapitel (refereegranskat)
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- Lisovski, Simeon, et al.
(författare)
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The roles of migratory and resident birds in local avian influenza infection dynamics
- 2018
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Ingår i: Journal of Applied Ecology. - : Wiley-Blackwell. - 0021-8901 .- 1365-2664. ; 55:6, s. 2963-2975
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Tidskriftsartikel (refereegranskat)abstract
- 1. Migratory birds are an increasing focus of interest when it comes to infection dynamics and the spread of avian influenza viruses (AIV). However, we lack detailed understanding of migratory birds' contribution to local AIV prevalence levels and their downstream socio-economic costs and threats. 2. To explain the potential differential roles of migratory and resident birds in local AIV infection dynamics, we used a susceptible-infectious-recovered (SIR) model. We investigated five (mutually non- exclusive) mechanisms potentially driving observed prevalence patterns: (1) a pronounced birth pulse (e.g. the synchronised annual influx of immunologically naive individuals), (2) short-term immunity, (3) increase in susceptible migrants, (4) differential susceptibility to infection (i.e. transmission rate) for migrants and residents, and (5) replacement of migrants during peak migration. 3. SIR models describing all possible combinations of the five mechanisms were fitted to individual AIV infection data from a detailed longitudinal surveillance study in the partially migratory mallard duck (Anas platyrhynchos). During autumn and winter, the local resident mallard community also held migratory mallards that exhibited distinct AIV infection dynamics. 4. Replacement of migratory birds during peak migration in autumn was found to be the most important mechanism driving the variation in local AIV infection patterns. This suggests that a constant influx of migratory birds, likely immunological naive to locally circulating AIV strains, is required to predict the observed temporal prevalence patterns and the distinct differences in prevalence between residents and migrants. 5. Synthesis and applications. Our analysis reveals a key mechanism that could explain the amplifying role of migratory birds in local avian influenza virus infection dynamics; the constant flow and replacement of migratory birds during peak migration. Apart from monitoring efforts, in order to achieve adequate disease management and control in wildlife-with knock-on effects for livestock and humans,-we conclude that it is crucial, in future surveillance studies, to record host demographical parameters such as population density, timing of birth and turnover of migrants.
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