Scale‐dependent climate signals drive breeding phenology of three seabird species

By M. Frederiksen, M. Harris, F. Daunt, P. Rothery, Sarah Wanless. 2004

244 citations recorded by the source corpus.

View Paper: https://www.semanticscholar.org/paper/316595880b583fafebc6893ed219edc0c62e66b8

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Citations in the corpus

Evidence for decrease in size of lesser sandeels Ammodytes marinus in a North Sea aggregation over a 30-yr period (2004, result): “…large (Wright 1996, Lewis et al. 2001), while examination of long-term trends in phenology indicate that breeding of kittiwakes on the Isle of May has become delayed by 5.1 d per decade (Frederiksen et al. 2004), a shift that is consistent with that seen in the timing of 0-group sandeels.”
Travelling through a warming world: climate change and migratory species. (2009, background): “Whereas sedentary birds appear to use local weather cues to determine timing of breeding, more dispersive species appear to respond to more extensive climate patterns (Forchhammer et al. 2002, Frederiksen et al. 2004).”
Multiple responses to increasing spring temperatures in the breeding cycle of blue and great tits (Cyanistes caeruleus, Parus major) (2011, background): “, 2008) few studies have combined these approaches by presenting detailed studies of more than one species (Visser et al., 2003; Frederiksen et al., 2004; Schaefer et al., 2006; Both & te Marvelde, 2007).”
Matches and mismatches: ocean climate, prey phenology and breeding success in a zooplanktivorous seabird (2008, background): “Seabirds, like other birds, are thought to strategically time their breeding in response to early season environmental 301 Mar Ecol Prog Ser 368: 295–304, 2008 cues that predict feeding conditions later in the season (Frederiksen et al. 2004).”
Shifts in phenology due to global climate change: the need for a yardstick (2005, background): “Black-legged kittiwake (Rissa tridactyla) and common guillemot (Uria aalge) laying dates have become later over the past two decades in a North Sea colony, while there has been no change in European shag (Phalacrocorax aristotelis) phenology (Frederiksen et al. 2004).”
Climate change and phenological responses of two seabird species breeding in the high-Arctic (2009, methodology): “The same relationship has been found for other Arctic kittiwake populations in Alaska (Murphy et al. 1991) and Canada (Gaston et al. 2005b), but not at lower latitudes in Scotland (Frederiksen et al. 2004).”
Impact of climate change on zooplankton communities, seabird populations and arctic terrestrial ecosystem—A scenario (2007, background): “There is some evidence of climate impact on the timing of reproduction, breeding success and population changes (e.g., Järvinen, 1994; Forchammer and Stenseth, 1998; McCleery and Perrins, 1998; Gjerdrum et al., 2003; Dunn, 2004; Fredriksen et al., 2004).”
Climatic effects on the breeding phenology and reproductive success of an arctic‐nesting goose species (2008, background): “…species of European birds, a positive NAO index, which is associated with warm spring temperatures, is related to early arrival date on breeding areas, early egg-laying (Sanz, 2002; Both et al., 2004; Frederiksen et al., 2004), and an increase in clutch size and offspring quality (M ller, 2002).”
Extrinsic and intrinsic determinants of winter foraging and breeding phenology in a temperate seabird (2005, background): “Although this relationship has disappeared in recent years (Frederiksen et al. 2004), we took the sine of wind direction to (a) remove circularity and (b) give easterly winds the maximum value of 1 and westerly winds the minimum value of −1.”