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Feeding Trips (feeding + trip)

Distribution by Scientific Domains

Life Sciences	100%

Selected Abstracts

Foraging behaviour and feeding locations of Rock Shags Phalacrocorax magellanicus from a colony in Patagonia, Argentina

IBIS, Issue 3 2001
FLAVIO QUINTANA
During 1996 and 1997, foraging Rock Shags Phalacrocorax magellanicus were studied at Punta Loma, Argentina using radio-transmitters deployed on ten adult shags during the chick-rearing period. Rock Shags undertook 2.6 ± 0.6 sd trips per day. The mean duration of a feeding trip was 2.6 ± 0.7 hours. A bird spent 36% of daylight hours away from the colony on feeding trips, diving for 92% of the foraging trip, and made a mean of 106 dives per foraging trip. Foraging trip duration was strongly correlated with the total number of dives made in one foraging trip. Rock Shags fed mainly in water less than 10m deep with a gravelly sand bottom and within 5 km of shore. Mean foraging range was 3.8 ± 2.6 km and 2.6 ± 2.3 km for 1996 and 1997, respectively. These results suggest a high foraging effort (diving time per foraging trip) for Rock Shags, presumably associated with poor food conditions close to the colony. Comparison is made with other Phalacrocorax species. [source]

The Influence of Exogenous Testosterone on the Dynamics of Nestling Provisioning in Dark-Eyed Juncos

ETHOLOGY, Issue 1 2007
Ethan D. Clotfelter
In many songbird species, application of exogenous testosterone (T) during the breeding season has the general effects of reducing male parental investment and increasing allocation of time and energy to mating. Most studies record the number of feeding trips made by males as a function of their hormone treatment, but few have investigated the ways in which testosterone affects the dynamics of male and female provisioning behavior or the quantity of food delivered by males. We attempt to fill these gaps in our understanding of testosterone and male parental effort by utilizing data from a long-term study on the behavioral endocrinology of the dark-eyed junco (Junco hyemalis). We found that male and female feeding rates covaried positively, although to different degrees, throughout the nestling period, but that this relationship was degraded in pairs in which males were given T implants. We also found that the coefficients of variation in the duration of intervals between successive feeding trips by males and females were highly positively related in broods of older nestlings. Male hormone treatment, however, had no effect on the coefficients of variation in either male or female feeding intervals. Finally, we examined the quantity of prey delivered by males and found no significant effect of hormone treatment. [source]

Foraging behaviour and habitat partitioning of two sympatric cormorants in Patagonia, Argentina

IBIS, Issue 3 2008
ESTEBAN FRERE
Radiotelemetry was used to assess the distribution and diving behaviour of Rock Shags Phalacrocorax magellanicus and Red-legged Cormorants Phalacrocorax gaimardi breeding in sympatry, and Rock Shags breeding in isolation. When breeding in sympatry there was little overlap in the foraging locations of the two species, with the highest densities of each species separated by 10 km. Red-legged Cormorants fed significantly closer to the breeding colony than did Rock Shags and undertook shorter foraging trips, making almost twice as many foraging trips per day as Rock Shags. Rock Shags breeding in isolation had a shorter foraging range than the birds breeding in sympatry with Red-legged Cormorants and foraging trip duration was significantly shorter. However, the number of feeding trips per day was similar between areas of sympatry and allopatry. Differences in the foraging ecology of Rock Shags in areas of sympatry and allopatry may be due to interspecific competition, which forces niche differentiation. The distance between foraging sites, the speed of movement of the prey, a species tendency to move into prey-depleted areas and the length of the breeding season (during which the birds are constrained to be in the same area) may play critical roles in determining the extent to which differential area use by competitors is a strategy that benefits both parties. [source]