Tracking Ocean Wanders (PDF, 5 MB) - BirdLife International
Tracking Ocean Wanders (PDF, 5 MB) - BirdLife International
Tracking Ocean Wanders (PDF, 5 MB) - BirdLife International
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waters. Main foraging areas were located over the<br />
continental shelf and slope south to 55ºS. During chickrearing,<br />
albatrosses mixed two strategies, short trips over<br />
the surrounding waters in southern Chile (similar to<br />
distribution during brooding), representing up to 90% of<br />
total trips, with long trips to central Chile (similar to those<br />
made during incubation) and Antarctic waters, mainly<br />
along the continental shelf and slope of the western<br />
Antarctic Peninsula. Despite the difference in trip<br />
characteristics between breeding stages, Black-browed<br />
Albatrosses tracked from Diego Ramirez foraged mainly<br />
over Chilean territorial waters, especially inside the EEZ<br />
waters during breeding, with very occasional forays into<br />
Argentine Patagonian Shelf waters.<br />
During incubation, birds tracked from Isla Ildefonso<br />
show a similar distribution to Diego Ramirez, with<br />
concentrations occurring off the Arauco Gulf, Los Chonos<br />
Archipelago (45ºS) and southern Chile (50–57ºS). This<br />
result is similar to that between Falkland Island (Malvinas)<br />
colonies during incubation.<br />
There is a strong interaction between breeding<br />
albatrosses and fishing vessels, which produce food through<br />
offal discards and cause mortality by incidental capture<br />
(Arata and Xavier 2003, Moreno et al. 2003). Thus, it seems<br />
likely that fishing boats could affect the normal distribution<br />
patterns of Black-browed Albatrosses in southern Chile and<br />
reduce inter-colony competition by food, allowing greater<br />
than normal levels of foraging range overlap.<br />
16<br />
<strong>Tracking</strong> ocean wanderers: the global distribution of albatrosses and petrels – Results<br />
Javier Arata and Graham Robertson<br />
Figure 3.7. Utilisation<br />
distribution maps for<br />
breeding Black-browed<br />
Albatrosses tracked from Isla<br />
Diego Ramirez at different<br />
stages in the breeding cycle.<br />
A. incubating birds<br />
(n=10,103 hrs); B. early<br />
breeding (incubation/<br />
brooding) (n=1,642 hrs);<br />
C. brooding (n=5,367 hrs);<br />
D. post guard (n=6,083 hrs).<br />
(Unable to determine number<br />
of individuals of each<br />
category from dataset, so<br />
sample sizes are only given<br />
in number of hours tracked).<br />
3.1.2 Distribution of breeding birds in relation to sex<br />
Northern and Southern Giant-petrels Macronectes halli<br />
and M. giganteus – South Georgia<br />
Giant-petrels are the largest birds of the family Procellariidae,<br />
weighing about 4–5 kg and with a wingspan of 150–210 cm.<br />
Both sibling species, the Northern Macronectes halli and the<br />
Southern M. giganteus, show a noticeable sexual size<br />
dimorphism in which males are between 16 and 35% heavier<br />
and have disproportionately larger bills than females<br />
(González-Solís 2004). The two species are the dominant<br />
scavengers of the Southern <strong>Ocean</strong>; males and females of<br />
both species rely mainly on penguin and pinniped carrion,<br />
but complement this diet by taking live seabirds, scavenging<br />
on food waste and feeding on marine prey such as<br />
crustaceans, cephalopods and fish (Hunter 1985).<br />
There is much evidence, from various sources, that both<br />
species of giant-petrels are among the more remarkable<br />
examples of sexual segregation in feeding habits in birds.<br />
Direct observation of feeding habits, diet analysis and stable<br />
isotope heavy metal studies, all suggest clear segregation in<br />
the trophic habits of males and females in both species<br />
(Hunter 1983, Becker et al. 2002, González-Solís et al. 2002b,<br />
González-Solís and Croxall 2005). Such sexual differences<br />
in the type of prey consumed imply a fundamental decision<br />
to direct the searching effort to particular habitats.<br />
This is well demonstrated in the areas exploited by each<br />
sex during the incubation period. In both species most males<br />
engaged in short trips close to the breeding grounds whereas<br />
most females foraged in pelagic waters further away from