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A recent study on the diving behaviour of European shags (Gulosus aristotelis (L.)) foraging in kelp forests off rocky coasts of Norway suggests surface durations are related only to the duration of the preceding dive, and hence are being used for respiratory recovery. These results contrast with earlier reports concerning shags foraging in highly tidal estuarine waters off the coast of Lundy Island, SW England, where there was a stronger relationship between dive durations and preceding pre‐dive surface durations, suggesting the use of preparatory variation in oxygen loading. These two datasets were collected using different methods, and statistically analysed in quite different ways, so the contrasting results here could be due to different methodologies rather than the ecological differences between the two foraging environments. Here, we re‐analyse the two datasets using similar statistical methods, and we confirm the contrasting results produced by the two datasets. We, therefore, conclude that shag breathing strategies do differ between these two marine environments, presumably reflecting adaptive facultatively plastic responses to differences in predictability of foraging dive durations. Off the Norwegian coast, unpredictable variation in the depth and availability of pelagic prey in complex environments may require more responsive post‐dive respiratory recovery on the surface after each dive. In the more uniform English near‐shore environment, however, pre‐dive preparatory oxygen loading customised to match predictable dive‐to‐dive variation in benthic prey depths and foraging durations, may be more time and energy efficient. [ABSTRACT FROM AUTHOR]

We tested the prediction that global warming has caused recent decreases in body weight (Bergmann's rule) and increases in wing length (Allen's rule) in 14 species of passerine birds at two localities in England: Wicken Fen (1968–2003) and Treswell Wood (1973–2003). Predicted long-term linear decreases in residual body weight occurred in four species: dunnocks (Wicken Fen), and great tits, blue tits and bullfinches (Treswell Wood). Non-linear decreases also occurred in reed warblers and blackcaps at Wicken Fen, which also had a surprising linear increase in residual body weight in blackbirds. Residual wing lengths increased linearly, as predicted, in six of seven species at Wicken Fen. Whereas there were non-linear long-term increases in wrens, dunnocks and blackbirds in Treswell Wood. Unexpected linear decreases also occurred in residual wing lengths in willow warblers (Wicken Fen), and blue tits, great tits and chaffinches (Treswell Wood). The most parsimonious explanation for such long-term changes in body weight is global warming, as predicted by Bergmann's rule. Greater site and species-specific effects on wing length (e.g. non-linear changes plus shorter wings in the woodland habitat) suggest a less straightforward conclusion concerning Allen's rule, probably because wing length involved variation in both bone and feather growth. Changes in residual body weights and wing lengths often differed between species and were sometimes non-linear, perhaps reflecting short-term modifications in selection pressures. Human-induced influences are discussed, such as avian predator population densities and land-use change. Short-term variation in temperature had little effect, but rainfall did explain the unusual increase in blackbird body weight, possibly as a result of improving food (earthworm) availability. [ABSTRACT FROM AUTHOR]