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Trip Duration (trip + duration)
Kinds of Trip Duration Selected AbstractsForaging behaviour and habitat partitioning of two sympatric cormorants in Patagonia, ArgentinaIBIS, Issue 3 2008ESTEBAN 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] Is food availability limiting African Penguins Spheniscus demersus at Boulders?IBIS, Issue 1 2006A comparison of foraging effort at mainland, island colonies The African Penguin Spheniscus demersus (Vulnerable) formed three new colonies during the 1980s, two on the South African mainland (Stony Point and Boulders) and one on Robben Island. One of the mainland colonies, at Boulders, Simon's Town, is in a suburban area, resulting in conflict with humans. Growth of the Boulders colony was initially rapid, largely through immigration, but has since slowed, possibly as a result of density-dependent effects either on land (where there has been active management to limit the spread of the colony) or at sea. We test the latter hypothesis by comparing the foraging effort of Penguins feeding small chicks at island and mainland sites, and relate this to the foraging area available to birds. Three-dimensional foraging paths of African Penguins were reconstructed using GPS and time,depth loggers. There were no intercolony differences in the rate at which birds dived during the day (33 dives/h), in diving depths (mean 17 m, max. 69 m) or in travelling speeds. The maximum speed recorded was 2.85 m/s, with birds travelling faster when commuting (average 1.18 m/s) than when foraging (0.93 m/s) or resting at sea (0.66 m/s during the day, 0.41 m/s at night). There were strong correlations between foraging trip duration, foraging range and total distance travelled. Foraging effort was correlated with chick age at Robben Island, but not at Boulders. Contrary to Ashmole's hypothesis, birds from Boulders (c. 1000 pairs) travelled further (46,53 km) and foraged for longer (13.2 h) than did birds from Robben Island (c. 7000 pairs) and Dassen Island (c. 21 000 pairs) (33 km, 10.3 h). The mean foraging range also differed significantly between mainland (18,20 km) and island colonies (9 km). The area available to central-place-foraging seabirds breeding on the mainland is typically less than that for seabirds breeding on islands, but the greater foraging range of Boulders birds results in an absolute foraging area roughly twice that of island colonies, and the area per pair is an order of magnitude greater for the relatively small Boulders colony. Ashmole's hypothesis assumes relatively uniform prey availability among colonies, but our results suggest this does not apply in this case. The greater foraging effort of Boulders birds probably reflects reduced prey availability in False Bay, and thus the recent slowing in growth at the colony may be the result of differential immigration rather than management actions to limit the spatial growth of the colony. [source] Foraging behaviour and feeding locations of Rock Shags Phalacrocorax magellanicus from a colony in Patagonia, ArgentinaIBIS, Issue 3 2001FLAVIO 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] Chick provisioning rates and growth in Blacklbrowed Albatross Diomedea melanophris and Grey-headed Albatross D. chrysostoma at Bird Island, South GeorgiaIBIS, Issue 4 2000NICOLAS HUIN We compared the parental division of labour and the pattern and rate of parental provisioning by two sympatric species of albatross of similar mass and breeding timetable but differing in diet and in the duration of chick-rearing. Using electronic weighing platforms inside artificial nests, we recorded chick mass of Black-browed Albatross and Grey-headed Albatross at Bird Island, South Georgia every 10 minutes for both species in 1993 and 1994 and for each species in two other years between 1990 and 1996. The chick mass data (nearly one million weighings) were used to calculate meal mass (over 5000 meals) and intervals between meals. Adult birds were fitted with radio-transmitters which allowed each meal to be allocated to the appropriate parent. The combination of meal mass and foraging trip duration were used to calculate provisioning rates for chicks and individual adults. Overall, Black-browed Albatrosses delivered significantly lighter meals (569 g) than Grey-headed Albatrosses (616 g) but more frequently (every 2.07 days and 2.50 days respectively). Thus combining foraging trip data for both parents, Black-browed Albatross chicks received a meal every 1.22 days compared with 1.26 days for Greyheaded Albatross. These rates did not differ significantly. The contribution of each sex of each species in chick provisioning fluctuated between years, being similar in some years or biased towards males in others. Chicks of both species that failed to fledge received smaller, less frequent meals than successful chicks. In 1990 and 1994, Black-browed Albatross chick provisioning rates were lower than in 1992 and 1993. In 1990, both meal mass and trip duration were affected, but only in 1994 was trip duration longer. Greyheaded Albatross chick provisioning rate was lower in 1994 than in other years but trip duration was longer. In each species, significant changes in meal mass and trip duration occurred within the chick-rearing period. Chick provisioning rates invariably declined before chicks attained their peak mass. For both species, chick growth rates and peak and fledging mass, but not fledging age, were affected by differences in provisioning rate. [source] Flipper bands do not affect foraging-trip duration of Magellanic PenguinsJOURNAL OF FIELD ORNITHOLOGY, Issue 4 2009P. Dee Boersma ABSTRACT Flipper bands are used to mark penguins because leg bands can injure their legs. However, concerns remain over the possible effects of flipper bands on penguins. We examined the effects of stainless-steel flipper bands on the duration of foraging trips by Magellanic Penguins (Spheniscus magellanicus) at Punta Tombo, Argentina, using an automated detection system. We predicted that, if bands were costly and increased drag, flipper-banded penguins would make longer foraging trips than those with small or no external markings. We tagged 121 penguins with radio-frequency identification (RFID) tags and an additional external mark. We placed either a stainless-steel band on the left flipper (N= 62) or a 2×10-mm small-animal ear tag in the outside web of the left foot (N= 59). We measured foraging-trip durations (N= 376 trips) for 68 adult penguins with chicks from 15 December 2007 to 28 February 2008. Contrary to predictions, trip duration was similar for banded and web-tagged penguins (P= 0.22) and for males and females (P= 0.52), with no interaction between tag type and sex (P= 0.52). No penguins marked in the 2007 breeding season and recaptured between 30 September and 30 November 2008 (N= 113) lost flipper bands or web tags, but three RFID tags failed between March and September 2008. Properly designed and applied flipper bands were a reliable marking method for Magellanic Penguins, had a lower failure rate than RFIDs, and did not affect foraging-trip duration. RESUMEN Los anillos de ala son usados para marcar pingüinos porque los anillos de tarso pueden causar heridas en sus piernas. Sin embargo, existen dudas sobre los posibles efectos de los anillos de ala sobre los pingüinos. Usando un sistema de detección automatizado, examinamos los efectos de anillos de ala hechos de acero inoxidable sobre la duración de los viajes para forrajeo por el pingüino Spheniscus magellanicus en Punta Tombo, Argentina. Predecimos que si los anillos afectarían a los pingüinos e incrementaran la fricción con el agua, los pingüinos con anillos de ala harían viajes para forrajeo de mayor duración en comparación a los que no portaban marcadores externos o que llevaban marcadores externos de menor tamaño. Marcamos a 121 pingüinos con marcadores de identificación por radio frecuencia, además de otro marcador al exterior del ave. Colocamos un anillo de acero inoxidable al ala izquierdo (N= 62), o un marcador de oreja (2×10 mm) para animales pequeños de en la membrana interdigital exterior del pie izquierdo (N= 59). Desde el 15 de diciembre del 2007 hasta el 28 de Febrero del 2008 medimos la duración de los viajes para forrajeo (N= 376 viajes) para 68 pingüinos adultos con pichones. Contrariamente a nuestras predicciones, la duración de los viajes fue similar para pingüinos con anillos y para pingüinos con marcadores en el pie (P = 0.22), así como entre machos y hembras (P= 0.52), con ninguna interacción entre el tipo de marca y el sexo (P= 0.52). Ningún pingüino marcado en la temporada reproductiva del 2007 y recapturado entre el 30 de Septiembre y el 30 de Noviembre del 2008 (N= 113) perdió el anillo de ala o el marcador en el pie, pero tres marcadores de identificación por radio frecuencia fallaron entre Marzo y Septiembre del 2008. Los anillos de ala apropiadamente diseñadas y aplicadas fueron un método de marcaje confiable para S. magellanicus, tuvieron una tasa de fallo menor a los marcadores de identificación por radio frecuencia y no afectaron a la duración de los viajes para forrajeo. [source] Growth in pups of the subantarctic fur seal (Arctocephalus tropicalis) on Amsterdam IslandJOURNAL OF ZOOLOGY, Issue 3 2000C. Guinet Abstract Growth in body mass in pups of the subantarctic fur seal Arctocephalus tropicalis was studied at Amsterdam Island, southern Indian Ocean during the rearing period between December 1995 and August 1996. We examined the change in the rates of mass gain and mass loss with pup age to explain the overall change in mass throughout the rearing period, when mothers alternate foraging trips at sea and attendance periods ashore. In the absence of their mothers, pups fast and lose mass. During the maternal attendance period ashore pups suck and gain mass. There was no significant difference in the rate of growth in mass between male and female pups. The rate of loss in mass during a fasting event was positively related to the initial body mass but negatively related to the age and duration of the fast of the pup. The rate of mass loss was best related to pup age by a quadratic relationship. The rate of mass loss increased until pups were 120 days old and then decreased until the end of the study period. The rate of gain in mass following a maternal foraging trip was positively related to the initial pup mass but negatively related to the foraging trip duration, and we found that the rate of mass gain decreased linearly with the age of the pup. The concomitant decrease in the rate of mass loss and mass gain for pups > 120 days old allowed pups to maintain a positive growth until they were 220 days old. After 220 days of age the rate of mass loss exceeded the rate of mass gain and the pups start to lose mass until weaning. [source] | ||||||||||