scholarly journals Health Assessment of Weddell Seals, Leptonychotes weddellii, in McMurdo Sound, Antarctica

2009 ◽  
pp. 123-138 ◽  
Author(s):  
P. K. Yochem ◽  
B. S. Stewart ◽  
T. S. Gelatt ◽  
D. B. Siniff
1996 ◽  
Vol 74 (9) ◽  
pp. 1775-1778 ◽  
Author(s):  
Jason F. Schreer ◽  
Kelly K. Hastings ◽  
J. Ward Testa

We examined mortality prior to weaning of Weddell seal pups (Leptonychotes weddellii), using resighting data collected from 1984 to 1993 on the annual ice of McMurdo Sound, Antarctica. Mortality rates were estimated using counts of dead pups found on the surface and mark–recapture techniques. The standard Jolly–Seber model for open populations fit the recapture data best and corresponded well to the known biology of these animals. Yearly mortality rates estimated by mark–recapture techniques ranged from 6 to 22%, with a mean across years of 13%. These values are twice as high as those previously reported for Weddell seals and those calculated from counts of dead pups in this study. This suggests that there is significant unseen mortality due either to undiscovered fatalities on the ice surface or to significant mortality occurring in the water.


1994 ◽  
Vol 72 (10) ◽  
pp. 1700-1710 ◽  
Author(s):  
J. Ward Testa

The movements and diving behavior of 18 adult female Weddell seals (Leptonychotes weddellii) were determined by satellite telemetry during the over-winter period in 1990 and 1991. Nine seals provided diving and movement data for 8 – 9 months. Seals that normally bred in the eastern part of McMurdo Sound spent most of the winter in the middle and northern parts of McMurdo Sound before the annual shore-fast ice had formed in those areas, or in the pack ice 0–50 km north of the sound and Ross Island. This is a greater use of pack ice, as opposed to shore-fast ice, in winter than was previously believed. Some long-distance movements (one over 1500 km in total) to the middle and northwestern parts of the Ross Sea also occurred. Although highly variable within and between individuals, dives indicative of foraging were primarily to mid-water regions (100 – 350 m) in both years, and were similar to those that have been observed in spring and summer, when Pleuragramma antarcticum is the primary prey of Weddell seals in McMurdo Sound.


2005 ◽  
Vol 17 (1) ◽  
pp. 71-72 ◽  
Author(s):  
S.L. KIM ◽  
K. CONLAN ◽  
D.P. MALONE ◽  
C.V. LEWIS

On the basis of observations of Weddell seals (Leptonychotes weddellii Lesson) made in the course of studying shallow-water benthic communities in McMurdo Sound, Antarctica, we suggest that caching and/or defence of uneaten food may be a strategy practiced by this animal. Such a phenomenon is uncommon but taxonomically widespread among vertebrates. Depending on circumstances, it is termed hoarding, caching, or storage and may be short- or long-term, include defence of the resource, or have other variable expressions, with the common threads being deferred consumption and deterrence of consumption by others (Vanderwall 1990). Many vertebrate taxa exhibit hoarding behaviour, including rodents (e.g. Sciuridae), carnivores (e.g. Canidae, Felinidae) and birds (e.g. Corvidae, Picidae). No form of food caching, to our knowledge, has ever been reported in a wild pinniped.


2004 ◽  
Vol 82 (4) ◽  
pp. 601-615 ◽  
Author(s):  
Michael F Cameron ◽  
Donald B Siniff

Since the 1960s, Weddell seals (Leptonychotes weddellii (Lesson, 1826)) have been tagged and surveyed annually in McMurdo Sound, Antarctica. Mark–recapture analyses and model selection trials using Akaike's Information Criterion indicate that sex, cohort, and year affect juvenile (ages 1 and 2) survival. In contrast, year and perhaps sex and cohort are less important factors for adult survival. Average annual survival is higher among adults (0.93) than juveniles (0.55–0.59) and there is little evidence for senescence to at least age 17. The oldest known-aged female and male in the study were 27 and 24 years old, respectively. Data suggest that the abundance of a resident population of Weddell seals remains relatively stable over time despite annual fluctuations in Jolly–Seber abundance estimates for the entire population. We argue that this annual variability is likely the result of temporary immigration of animals born outside the study area; mean rates are estimated from a simulation model and tagging data to be between 16.8% and 39.7% for females and between –13.1% and 31.6% for males. Sea ice extent appears to affect immigration where, during times of reduced fast-ice, immigrants are forced, or allowed easier access, into the ice-covered areas of Erebus Bay from surrounding locations. Our findings contradict previous studies reporting lower survival and higher immigration. Model choice is shown to be the most likely cause of these discrepancies and we provide evidence that our models are more appropriate than those used elsewhere.


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