7 research outputs found

    Seasonal Sexual Segregation by Monomorphic Sooty Shearwaters Puffinus griseus Reflects Different Reproductive Roles during the Pre-Laying Period

    Get PDF
    Tracking technology has revolutionized knowledge of seabird movements; yet, few studies have examined sex differences in distribution and behavior of small to medium-sized, sexually-monomorphic seabirds. Application of bird-borne geolocation-immersion loggers revealed seasonal segregation in the sexually-monomorphic Sooty Shearwater Puffinus griseus, mainly in the pre-laying period, when there were clear differences in reproductive roles. Shearwaters first returned to the Falkland Islands on 27 Sept±8 d; males, on average, 8 d earlier than females. Prior to egg-laying, distribution at sea, colony attendance and behaviour depended on sex. Males foraged locally over the southern Patagonian Shelf and Burdwood Bank, spending mainly single days at sea and intervening nights in the burrow. Females, who flew for more of the day during this time, foraged in more distant areas of the northern Patagonian Shelf and Argentine Basin that were deeper, warmer and relatively more productive. Attendance of females at the colony was also more variable than that of males and, overall, males were present for significantly more of the pre-laying period (38 vs. 19% of time). Sex differences were reduced following egg-laying, with males and females using similar foraging areas and making trips of similar mean duration in incubation (7.6±2.7 d) and chick-rearing (1.4±1.3 d). Congruence continued into the non-breeding period, with both sexes showing similar patterns of activity and areas of occupancy in the NW Atlantic. Thus, seasonal changes in reproductive roles influenced patterns of sexual segregation; this occurred only early in the season, when male Sooty Shearwaters foraged locally, returning regularly to the colony to defend (or maintain) the burrow or the mate, while females concentrated on building resources for egg development in distant and relatively more productive waters

    Feeding and foraging ecology of Trindade petrels Pterodroma arminjoniana during the breeding period in the South Atlantic Ocean

    No full text
    Seabirds breeding in tropical environments experience high energetic demands, when foraging in an oligotrophic environment. The globally threatened Trindade petrel Pterodroma arminjoniana has its largest colony in Trindade Island (20°30′S–29°19′W) inside the oligotrophic South Atlantic Subtropical Gyre. Diet sampling methods, geolocator tracking and stable isotope analysis were used to describe its diet, compare foraging trips and distributions, and assess temporal variations in the trophic niche throughout the breeding period. Diet consisted mainly of squid and fish. The high species diversity and wide range of prey sizes consumed suggests the use of multiple foraging techniques. Stable isotope mixing models confirm that Trindade petrels rely mainly on squid throughout the breeding period. Its broad isotopic niche seems to reflect both a diverse diet and foraging range, since birds can reach up to 3335 km from the colony. Isotopic niche showed limited variation even in an 8-year interval, apparently due to oceanographic stability, although changes in the isotopic niche have demonstrated an adjustment to different conditions in different seasons. Petrels change foraging areas and prey during the breeding period: pre-incubating birds use more productive areas west of Trindade Island and obtain low trophic position prey; incubating petrels perform longer trips southward to consume prey of high trophic position; and chick-rearing petrels use areas around the island. These results demonstrate that to deal with high demand breeding in a colony surrounded by oligotrophic waters, Trindade petrels need to explore wide foraging areas and utilize a diverse diet, besides adjusting trophic niche according to breeding stage

    The m�canique physique of sim�on denis Poisson: The evolution and isolation in France of his approach to physical theory (1800?1840)

    No full text
    corecore