Resources for Long Distance Migration: Intertidal Exploitation of Littorina and Mytilus by Knots Calidris Canutus in Iceland

Oikos ◽  
1992 ◽  
Vol 65 (2) ◽  
pp. 179 ◽  
Author(s):  
Thomas Alerstam ◽  
Gudmundur A. Gudmundsson ◽  
Kerstin Johannesson
1996 ◽  
Vol 69 (1) ◽  
pp. 191-217 ◽  
Author(s):  
Theunis Piersma ◽  
Leo Bruinzeel ◽  
Rudolf Drent ◽  
Marcel Kersten ◽  
Jaap Van der Meer ◽  
...  

Ibis ◽  
2005 ◽  
Vol 147 (4) ◽  
pp. 738-749 ◽  
Author(s):  
PHILIP W. ATKINSON ◽  
ALLAN J. BAKER ◽  
RICHARD M. BEVAN ◽  
NIGEL A. CLARK ◽  
KIMBERLY B. COLE ◽  
...  

Ibis ◽  
2008 ◽  
Vol 133 (2) ◽  
pp. 140-152 ◽  
Author(s):  
GUDMUNDUR A. GUDMUNDSSON ◽  
ÅKE LINDSTRÖM ◽  
THOMAS ALERSTAM

2007 ◽  
Vol 363 (1490) ◽  
pp. 247-266 ◽  
Author(s):  
Deborah M Buehler ◽  
Theunis Piersma

Long-distance migration, and the study of the migrants who undertake these journeys, has fascinated generations of biologists. However, many aspects of the annual cycles of these migrants remain a mystery as do many of the driving forces behind the evolution and maintenance of the migrations themselves. In this article we discuss nutritional, energetic, temporal and disease - risk bottlenecks in the annual cycle of long-distance migrants, taking a sandpiper, the red knot Calidris canutus , as a focal species. Red knots have six recognized subspecies each with different migratory routes, well-known patterns of connectivity and contrasting annual cycles. The diversity of red knot annual cycles allows us to discuss the existence and the effects of bottlenecks in a comparative framework. We examine the evidence for bottlenecks focusing on the quality of breeding plumage and the timing of moult as indicators in the six subspecies. In terms of breeding plumage coloration, quality and timing of prealternate body moult (from non-breeding into breeding plumage), the longest migrating knot subspecies, Calidris canutus rogersi and Calidris canutus rufa , show the greatest impact of bottlenecking. The same is true in terms of prebasic body moult (from breeding into non-breeding plumage) which in case of both C. c. rogersi and C. c. rufa overlaps with southward migration and may even commence in the breeding grounds. To close our discussion of bottlenecks in long-distance migrants, we make predictions about how migrants might be impacted via physiological ‘trade-offs’ throughout the annual cycle, using investment in immune function as an example. We also predict how bottlenecks may affect the distribution of mortality throughout the annual cycle. We hope that this framework will be applicable to other species and types of migrants, thus expanding the comparative database for the future evaluation of seasonal selection pressures and the evolution of annual cycles in long-distance migrants. Furthermore, we hope that this synthesis of recent advancements in the knowledge of red knot annual cycles will prove useful in the ongoing attempts to model annual cycles in migratory birds.


Author(s):  
Jesse Conklin ◽  
Yvonne Verkuil ◽  
Philip Battley ◽  
Chris Hassell ◽  
James Johnson ◽  
...  

Present-day ecology and population structure are the legacies of past climate and habitat perturbations, and this is particularly true for species that are widely distributed at high latitudes. The red knot, Calidris canutus, is an arctic-breeding, long-distance migratory shorebird with six recognized subspecies defined by differences in morphology, migration behavior, and annual-cycle phenology, in a global distribution thought to have arisen just since the Last Glacial Maximum (LGM). We used nextRAD sequencing of 10,881 single-nucleotide polymorphisms (SNPs) to assess the neutral genetic structure and phylogeographic history of 172 red knots representing all known global breeding populations. Using population genetics approaches, including model-based scenario-testing in an approximate Bayesian computation (ABC) framework, we infer that red knots derive from two main lineages that diverged ca. 34,000 years ago, and thus persisted at the LGM in both Palearctic and Nearctic refugia, followed by at least two instances of secondary contact and admixture. In two flyways, we detected clear genetic structure between population pairs with similar migrations and substantial geographic overlap in the non-breeding season. Conversely, other populations were only weakly differentiated despite clearly divergent migratory phenotypes and little or no apparent contact throughout the annual cycle. In general, the magnitude of genetic differentiation did not match that of phenotypic differences among populations, suggesting that flyway-specific phenotypes developed quite rapidly and do not necessarily impose barriers to gene flow. Our results suggest that population structure and migratory phenotypes in red knots arose from a complex interplay among phylogeography, plasticity, and selective processes.


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