Seasonal haulout patterns of crabeater seals (<Emphasis Type="Italic">Lobodon carcinophaga</Emphasis>)

The haulout patterns of five adult and two juvenile crabeater seals (Lobodon carcinophaga) were documented from February to December 1995 in three areas of the Antarctic. The longest haulout event was 19.2 h (mean=7.9, median=7.8); the longest in-water event was 85.8 h (mean=15.1, median=14.2). In no month were more than 76% of the adult seals in our sample hauled-out simultaneously. Multivariate repeated measures analysis of variance tests revealed no difference between males and females in the daily timing of haulout (P>0.05) between March and August (the only months with an adequate sample); in contrast, haulout timing differed between juvenile and adult seals (P<0.05) except in May. Juveniles spent about twice as much time hauled-out on the ice as adults (38% vs 20%, respectively; P<0.05). Predator avoidance by juveniles is hypothesized to be a possible cause for these differences. In light of these haulout patterns, population surveys of crabeater seals conducted in February, and as close as possible to local solar noon, can be expected to encounter the highest proportion of seals hauled-out on ice.

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Counts of southern elephant seals, Mirounga leonina, at Bouvet Island

Southern elephant seals were counted and classified into subjective sex-age classes on a weekly basis during expeditions to Bouvet Island in the austral summers of 1996/1997 and 1998/1999. The expeditions coincided with the moulting period of elephant seals aged one?year and older. The presence of weaned pups at the principal haulout site, Nyrøysa/Westwindstranda, during the latter expedition, indicates that breeding took place here during 1998. Elephant seal counts from previous expeditions are summarised.     

Unmarked individuals in mark–recapture studies: Comparisons of marked and unmarked southern elephant seals at Marion Island

The presence of unmarked individuals is common in mark–recapture study populations; however, their origin and significance in terms of population dynamics remain poorly understood. At Marion Island, southern Indian Ocean, where virtually all southern elephant seal Mirounga leonina pups born annually (1983–2008) were marked in a long‐term mark–resight study, large numbers of unmarked seals occur. Unmarked seals originate either from marker (tag) loss or from immigration. We aimed to identify patterns in the occurrence of marked and unmarked individuals that will allude to the possible origin and significance of the untagged component of the population, predicting that tag loss will add untagged seals to mainly adult age categories whereas migrating untagged individuals will be mostly juveniles. We fitted a generalized linear model using the factors month, year and age‐class to explain the relative abundance of untagged seals (tag ratio) from 1997 to 2009. Site usage of untagged seals relative to tagged seals was assessed using a binomial test. Untagged seals, predominantly juveniles, were present in the highest proportions relative to tagged seals during the winter haulout (tagged seals/total seals less than 0.3) and the lowest proportion (approximately 0.5) during the female breeding haulout, increasing in relative abundance from 1997 to 2009. Untagged seals were distributed evenly across suitable haulout sites while tagged seals displayed high local site fidelity and occurred in greater numbers at or near large breeding beaches. Untagged seals are considered to be mostly migrant seals that disperse from other islands within the southern Indian Ocean and haul out at Marion Island during non‐breeding haulouts in particular. Some of these seals immigrate to the breeding population, which can be a key component of the local population dynamics. We emphasize the need for mark–recapture studies to evaluate the role of the unmarked component of a population, thereby inducing a more confident estimation of demographic parameters from the marked sample.     

Dispersion during the moult haulout of southern elephant seals at the Courbet Peninsula, Iles Kerguelen

We studied the dispersion of 4-year-old southern elephant seals (Mirounga leonina) along a 75.5 km coastal area at the Courbet Peninsula, Iles Kerguelen, relative to their birth site when they were ashore to moult in early 1984. The seals were mostly faithful to their natal sites, but availability of suitable moulting habitat (e.g. wallows, vegetated areas) influenced seal dispersion. As moult progressed, the seals moved farther away from their initial moult sites and natal sites, but remained largely on the easterly beaches of the Courbet Peninsula. This behaviour would facilitate mark-recapture estimates of age and sex specific survival.     

Timing of mating in the Common Seal (Phoca vitulina)

It is generally believed that British Common Seals mate after the moult, in late summer. In contrast, evidence from other parts of their range suggests that mating occurs before the moult, at the end of lactation. This paper reviews the evidence for the timing of mating from all parts of the range of this species, and presents data on seasonal changes in male sexual behaviour at a haulout site in Orkney, U.K. British Common Seals do mate at the end of lactation, as in other areas; the presumed precopulatory display described in previous studies is more likely to have been play between juveniles or sub-adults.     

THE DISTRIBUTION, ABUNDANCE AND SELECTED PREY OF THE HARBOR SEAL, PHOCA VITULINA CONCOLOR, IN SOUTHERN NEW ENGLAND

The seasonal distribution and abundance of harbor seals occurring south of Maine were documented by counting the number of seals at traditional haulout locations. The average number of seals counted during each survey in Massachusetts and New Hampshire was 3,560 ± 255 (95% CI), 1983–1987. The maximum number of seals counted on any individual survey was 4,736 individuals. Fifty percent of all the surveys since January 1985 have resulted in counts greater than 4,000 seals reflecting a 27% increase in the abundance of seals in our study area since that date. Seventy-five percent of the seals in southern New England are located at haulout sites on Cape Cod and Nantucket Island. The largest aggregation of seals in the eastern United States occurs mid-winter at Monomoy Island and adjacent shoals. A single high count of 1,672 seals occurred at this site during the study period. An additional 271–374 seals were also counted in Rhode Island, Connecticut and eastern Long Island Sound during surveys conducted in March 1986 and 1987. The American sandlance Ammodytes americanus was the single dominant prey item of harbor seals in waters adjacent to Cape Cod based on the modified frequency of occurrence of each prey species in scat samples collected from three haulout sites on Cape Cod between 1984–1987. During January and February sandlance was the near exclusive prey item at Monomoy (99%, n= 80). During March and April, the frequency of Atlantic herring Clupea harengus increased in the scat samples at this site. Regional differences in the diet of seals reflect distinct prey communities throughout the study area. Since 1986, the percent occurrence and importance of sandlance in the diet of seals has decreased, reflecting an overall decrease in abundance of this prey species in waters adjacent to Cape Cod. In spite of fluctuations in abundance, and regional differences in the diet of seals throughout the study area, sandlance still comprised a minimum 55% of the total prey species of harbor seals throughout the study area.     

Growth and population parameters of the world’s northernmost harbour seals Phoca vitulina residing in Svalbard, Norway

The harbour seals (Phoca vitulina) in Svalbard are the northernmost population of this species. The population size is thought to be less than 1,000 individuals; these animals reside principally within a national park on Prins Karls Forland on the west coast of Spitsbergen, Svalbard, at about 78°20N. The material presented in this study was collected from 367 live-captured animals, aged based on growth layers read from stained, decalcified incisor sections (except for pups of the year). Standard length (F_1,246=45.70, P<0.0001) and body mass (F_1,258=25.28; P<0.0001) were both significantly influenced by sex when age was taken into account. Adult males are both longer [152.9±4.8 (SE) vs 140.1±2.0 cm, standard length] and heavier (104.0±5.0 vs 83.2±2.7 kg, body mass) than adult females in this population. Age at sexual maturity was assessed based on analyses of sex hormones. Testosterone levels in males showed an abrupt increase at 6 years of age, while estradiol levels in females increased from age 4. The reproductive rate of adult females was 0.93. The longevity of Svalbard harbour seals was short compared to harbour-seal populations from other areas. However, these seals are not exposed to terrestrial predation; there is no known mortality due to fisheries or hunting and their pollution burdens are low. Extreme seasonality and perhaps other harsh environmental conditions at the northern edge of this species distribution may exert long-term low levels of stress that result in short life span, or there are currently unknown acute sources of mortality in this population. To our knowledge, this is the first study of population parameters on a pinniped species using cross-sectional, non-terminal sampling.     

Distribution and diving behaviour of harp seals (<Emphasis Type="Italic">Pagophilus groenlandicus</Emphasis>) from the Greenland Sea stock

The distribution and diving behaviour of 16 adult harp seals (Pagophilus groenlandicus) from the Greenland Sea stock were studied in 1993 and 1999, using satellite-linked dive recorders (SDRs). The seals remained near the pack-ice edge in the Greenland Sea between breeding and moulting (April/May 1993; 6F) and during the first 7 weeks after moulting (June/July, 1999; 4F, 6M), there diving to depths of <100 m. In mid-July 1999, seven out of eight seals with active SDRs migrated into the Barents Sea, there diving to <400 m and sharing feeding grounds with the Barents Sea harp seal stock. Between September and December, six of these seals joined the eighth seal in the Denmark Strait until March 2000, there diving to depths of 100–400 m. Overall, dives were significantly deeper in the day and in winter than at night and in summer, with some regional differences. Harp seals are considered pack-ice-associated seals, but our tagged seals spent a considerable proportion of their time in open water, their distribution largely overlapping with that of capelin (Mallotus villosus).     

Molecular methods for differentiating grey seal (Halichoerus grypus) and harbour seal (Phoca vitulina) scat

Pinniped dietary information is crucial for understanding marine ecosystems; however, in the North Atlantic, grey and harbour seals haulout concomitantly and their faeces are visually indistinguishable. Therefore, we developed molecular methods to differentiate the species' scat. PCR primers were created that amplify a portion of mitochondrial 16S ribosomal DNA in grey and harbour seals. The samples were amplified and the resulting products were digested using the restriction enzyme Tsp509I, producing diagnostic banding patterns. These tools provide a mechanism by which separate dietary analysis can be achieved for grey and harbour seals at mixed haulouts in New England.     

Movements and diving of bearded seal (Erignathus barbatus) mothers and pups during lactation and post-weaning

Eleven bearded seals (Erignathus barbatus) were tagged with satellite-linked dive recorders in Kongsfjorden, Svalbard, Norway, in May 1994. These animals included four mother-pup pairs and three single pups. The seals were tracked for 21–258 days. A total of ˜207,000 dives were recorded. Bearded seal mothers showed limited movements during the nursing and moulting periods. After weaning, the pups moved out of the tagging area and dispersed coastally. One pup left Svalbard and moved far offshore to Greenland and Jan Mayen. Bearded seal adults displayed a bi-modal dive behaviour, with peaks of activity that were shallower than 10 m or from 50 to 70 m. Most dives for adult seals (97%) were shorter than 10 min. Young pups performed dives that were shallower and shorter in duration than their accompanying mothers, but diving skills improved rapidly with age. Six of the seven pups dived deeper than 448 m by the time they were 2 months old. Analyses of movement data with respect to separation of mother-pup pairs suggest a lactation period of about 24 days. Accepted: 31 January 2000     

Movements of adult female Weddell seals during the winter months

The focus of this study was the distribution of adult female Weddell seals during winter at the Vestfold Hills. Satellite tracking of Weddell seals had never been done before at this location. Hence, this was a pilot study to evaluate the following methods. We attached satellite transmitters to the lower back, where there was least potential to change the seals’ behaviour or to damage instruments on the ice. Location data were obtained only where the seals hauled out, not necessarily where they were feeding. All locations were within the area of fast-ice that was associated with the Vestfold Hills. There were gaps of up to 30 days in the location data sets. Each instrument (n=3) remained attached and functioning for ca. 6 months. During that time, two of the three seals hauled out within small areas adjacent to, or nearby, open water. The same seals hauled out sporadically. We inferred that these seals foraged offshore whilst returning to fast-ice to rest. If Weddell seals forage beneath dynamic ice but return to stable ice as their preferred resting substrate, then evidence of haulout sites will always be a biased measure of foraging range. Tracking seals in the water may be possible using alternative placement of transmitters. However, there is potential for instruments to interfere with movement (breathing and prey capture). For this reason, we recommend a combination of sensors, diet and tracking haulout sites to research winter foraging.     

7. SHORT NOTES FROM MEMBERS

Cooper, J., Ross, G. J. B. &; Shaughnessy, P. D. 1978. Seasonal and spatial distribution of Rockhopper Penguins ashore in South Africa. Ostrich 49:40-44. There are 30 records of Rockhopper Penguins Eudyptes chrysocome ashore in South Africa. Both the southern subspecies E.c. chrysocome, and the northern subspecies E.c. moseleyi have been recorded. The northern subspecies has occurred more frequently. Most records are of moulting juveniles in January and February. Records of adult birds are more scattered throughout the year. Rockhopper Penguins in South Africa have been recorded only south of 30S. Birds of the northern subspecies probably originate from South Atlantic islands (Tristan da Cunha group and Gough). Birds of the southern subspecies are probably from the Prince Edward Islands.     

PUPPING PHENOLOGY AND DEMOGRAPHY OF HARBOR SEALS (PHOCA VITULINA RICHARDSI)ON TUGIDAK ISLAND, ALASKA

The number of seals on shore at Tugidak Island (Gulf of Alaska) declined 72%–85% between 1976 and 1988 and increased during the 1990s. We compared pupping phenology and the ratio of pupping-period counts to molting-period counts between declining (1976–1979) and increasing (1994–1998) years, and examined the sex/age structure of seals ashore during the 1990s. In the 1970s the onset and peak of pupping occurred 6–18 d later than in the 1990s. Rate of pup abandonment was higher in 1978 than in the 1990s. Between 1994 and 1995, the maximum and mean number of seals ashore increased >50%, largely due to an increase in non-pups. From 1995 to 1998, the sex/age structure of seals ashore was similar among years. We observed three to four times as many seals during the molting period than during the pupping period in the 1970s, whereas similar numbers were ashore during these periods in the 1990s, perhaps reflecting changes in demography and/or haul-out behavior. Changes in pupping phenology and demography may reflect environmental changes, such as food availability, and when monitored in conjunction with population counts, may help us better interpret changes in the number of seals ashore.     

Population changes of Antarctic fur seals at Nyrøysa, Bouvetøya

Antarctic fur seal Arctocephalus gazella pup production at Nyrøysa, Bouvetøya was estimated to be approximately 15,000 per annum during each of four summers from 1996 to 2002, indicating a total population of about 66,000. While the Bouvetøya population is the second largest for this species, pup production at this site still accounts for only 2.4% of the global total. This population experienced a mean annual rate of increase of 30.6% for the period 1989–1996, perhaps due, in part, to significant immigration, but has been stable since 1996. Historical accounts of significant numbers of animals being present towards the end of the period of sealing (C.1800–1930), indicate that the geographic isolation and inaccessibility of this site may have resulted in the Bouvetøya population being one of three populations that survived a series of periods of extreme exploitation of this species.     

Ringed and bearded seal densities in the eastern Chukchi Sea, 1999–2000

Aerial surveys were conducted in 1999 and 2000 to estimate the densities of ringed (Phoca hispida) and bearded (Erignathus barbatus) seals in the eastern Chukchi Sea. Survey lines were focused mainly on the coastal zone within 37 km of the shoreline, with additional lines flown 148–185 km offshore to assess how densities of seals changed as a function of distance from shore. Satellite-linked time-depth recorders were attached to ringed seals in both years to evaluate the time spent basking on the ice surface. Haulout patterns indicated that ringed seals transitioned to basking behavior in late May and early June, and that the largest proportion of seals (60–68%) was hauled out between 0830 and 1530 local solar time. Ringed seals were relatively common in nearshore fast ice and pack ice, with lower densities in offshore pack ice. The average density of ringed seals was 1.91 seals km⁻² in 1999 (range 0.37–16.32) and 1.62 seals km⁻² in 2000 (range 0.42–19.4), with the highest densities of ringed seals found in coastal waters south of Kivalina and near Kotzebue Sound. The estimated abundance of ringed seals for the entire study area was similar in 1999 (252,488 seals, SE=47,204) and 2000 (208,857 seals, SE=25,502). Bearded seals were generally more common in offshore pack ice, with the exception of high bearded seal numbers observed near the shore south of Kivalina. Bearded seal densities were not adjusted for haulout behavior, and therefore, abundance was not estimated. Unadjusted average bearded seal density was 0.07 seals km⁻² in 1999 (range 0.011–0.393) and 0.14 seals km⁻² in 2000 (range 0.009–0.652). Levels of primary productivity, benthic biomass, and fast ice distribution may influence the distributions of ringed and bearded seals in the Chukchi Sea. Information on movement and haulout behavior of ringed and bearded seals would be very useful for designing future surveys.     

Influence of time of day and month on Weddell seal haul-out patterns at the Vestfold Hills, Antarctica

A diurnal pattern in haul-out behaviour has been described for Weddell seals at McMurdo Sound, Antarctica, but regional and seasonal variations were previously unknown. Knowledge of activity patterns is important for standardising census methods and census data. This study quantified the diurnal pattern in haul-out behaviour of Weddell seals at the Vestfold Hills from October 1994 to March 1995. Sequential counts of seals on the ice showed that, between 0900 and 1930 hours, seal abundance differed up to 95%. Fewer seals were hauled out in the morning than in the afternoon. The maximum numbers of seals were hauled out at the warmest time of day. The diurnal cycle was less pronounced in the breeding season than in the moulting season. The findings indicated the importance of censusing Weddell seals after 1430 hours and before 1700 hours local time, especially in the moulting season. Correction factors are given for month and time of day. Received: 27 November 1996 / Accepted: 1 May 1997     

The prevalence of Toxoplasma gondii in polar bears and their marine mammal prey: evidence for a marine transmission pathway?

Little is known about the prevalence of the parasite Toxoplasma gondii in the arctic marine food chain of Svalbard, Norway. In this study, plasma samples were analyzed for T. gondii antibodies using a direct agglutination test. Antibody prevalence was 45.6% among polar bears (Ursus maritimus), 18.7% among ringed seals (Pusa hispida) and 66.7% among adult bearded seals (Erignathus barbatus) from Svalbard, but no sign of antibodies were found in bearded seal pups, harbour seals (Phoca vitulina), white whales (Delphinapterus leucas) or narwhals (Monodon monoceros) from the same area. Prevalence was significantly higher in male polar bears (52.3%) compared with females (39.3%), likely due to dietary differences between the sexes. Compared to an earlier study, T. gondii prevalence in polar bears has doubled in the past decade. Consistently, an earlier study on ringed seals did not detect T. gondii. The high recent prevalence in polar bears, ringed seals and bearded seals could be caused by an increase in the number or survivorship of oocysts being transported via the North Atlantic Current to Svalbard from southern latitudes. Warmer water temperatures have led to influxes of temperate marine invertebrate filter-feeders that could be vectors for oocysts and warmer water is also likely to favour higher survivorship of oocycts. However, a more diverse than normal array of migratory birds in the Archipelago recently, as well as a marked increase in cruise-ship and other human traffic are also potential sources of T. gondii.