Body and organ mass dynamics during remigial moult in a wing–foot-propelled diving sea duck: the Common Eider (Atlantic) (Somateria mollissima dresseri)

Body and organ dynamics, during remigial moult, have been mainly explored on geese, dabbling ducks, and foot-propelled diving ducks, but weakly on sea ducks. This study investigated the internal changes in a wing–foot-propelled sea duck to determine the adaptive strategies implemented. Forty-five male Common Eiders (Atlantic) (Somateria mollissima dresseri Sharpe, 1871), collected in the Gulf of St. Lawrence, were dissected; their body mass, muscle mass, and organ sizes were measured. We tested three hypotheses: (1) S. m. dresseri use a strategic reduction of body mass to reduce the flightlessness duration; (2) organs will exhibit changes consistent with a trade-off between function and maintenance to save and reallocate energy and proteins to feather growth; (3) S. m. dresseri would show lower flight muscle reduction than foot-propelled diving ducks. Somateria mollissima dresseri did not lose body mass, which does not support the first hypothesis. Atrophy of the heart followed by hypertrophy and opposite changes in leg muscle mass and gizzard mass are consistent with the second hypothesis. Flight muscle mass showed lower variations than in other ducks, validating the third hypothesis. We also suggest that the lipid depletion observed early in the moult could be a strategy to reduce foraging effort and minimize the risk of damaging the growing feathers.

Phenology and duration of remigial moult in Surf Scoters (Melanitta perspicillata) and White-winged Scoters (Melanitta fusca) on the Pacific coast of North America

By quantifying phenology and duration of remigial moult in Surf Scoters ( Melanitta perspicillata (L., 1758)) and White-winged Scoters ( Melanitta fusca (L., 1758)), we tested whether timing of moult is dictated by temporal optima or constraints. Scoters (n = 3481) were captured during moult in Alaska, British Columbia, and Washington, and remigial emergence dates were determined. We provide evidence for a pre-emergence interval of 7.3 days that occurs after old primaries are shed and before new ones become visible. All age and sex classes of both scoter species exhibited a wide range of emergence dates (Surf Scoters: 26 June to 22 September; White-winged Scoters: 6 July to 21 September) suggestive of a lack of strong temporal optima for remigial moult. For both species, timing of moult was influenced by site, year, age, and sex. Relative to other waterfowl species, scoters have typical remigial growth rates (Surf Scoters: 3.9 mm·day–1; White-winged Scoters: 4.3 mm·day–1) but a long flightless period (34–49 days), in part because their relatively high wing-loading requires a greater proportion of feather regrowth to regain flight. Our data suggest that moulting scoters are not under strong selective pressure to complete moult quickly.