Birth to weaning: parturition, duration of lactation, and attendance cycles of Australian sea lions (Neophoca cinerea)

1993 ◽  
Vol 71 (10) ◽  
pp. 2047-2055 ◽  
Author(s):  
Lesley V. Higgins ◽  
Leila Gass

Parturition, time to weaning, and female attendance patterns were studied over four breeding seasons in Australian sea lions, Neophoca cinerea, on Kangaroo Island, South Australia. Females generally exhibited site fidelity in their choice of birth sites, and arrived a mean of 1.8 days prior to birth. After birth, females stayed ashore a mean of 9.8 days before departing on their first foraging trip. Trips to sea were about 48 h in length although there was significant variation over time. Stays ashore were about 33 h long and were much less varied than trips to sea. Females moved pups away from the natal areas after about 1 month, and began spending less time with them while they were ashore. Linked with the extended breeding cycle of 17.6 months was an equally long period of maternal investment. Females suckled their pups for 15 – 18 months, or until about 1 month before the next birth. Twenty-nine percent of females did not pup consecutively each breeding season, but continued to suckle their offspring until the next birth, some for as long as 40 months.

2013 ◽  
Vol 61 (2) ◽  
pp. 112 ◽  
Author(s):  
Peter D. Shaughnessy ◽  
Simon D. Goldsworthy ◽  
Paul Burch ◽  
Terry E. Dennis

The Australian sea lion is an Australian endemic, restricted to South Australia and Western Australia, with 86% of the population in South Australia. It was listed under the Commonwealth Environment Protection and Biodiversity Conservation Act as Vulnerable in February 2005, and the International Union for the Conservation of Nature has listed it as Endangered. Sea lions are taken as bycatch in the gill-net fishery for school shark and gummy shark, and the risk of extinction of breeding colonies is high even from low levels of bycatch. We assessed trends in pup population size at The Pages Islands, a large breeding colony in South Australia. Pup abundance was estimated by direct counting of live and dead pups; the maximum count in each breeding season was used for trend analysis. The average of direct counts of pups in 14 breeding seasons between 1989–90 and 2009–10 was 473 (s.d. = 58.4). There was no trend in pup numbers, contrasting with two other large colonies: Seal Bay, Kangaroo Island (decreasing), and Dangerous Reef (increasing since 2000). The Australian Sea Lion Management Strategy of the Australian Fisheries Management Authority aims to reduce sea lion bycatch in the shark fishery; a key item is a fishery closure around each breeding colony in South Australia. Implementation of the closure around The Pages should lower the risk of bycatch of its sea lions with foraging areas that previously overlapped with the fishery and should allow the colony’s population size to increase.


1992 ◽  
Vol 19 (4) ◽  
pp. 405 ◽  
Author(s):  
NJ Gales ◽  
AJ Cheal ◽  
GJ Pobar ◽  
P Williamson

The Australian sea-lion, Neophoca cinerea, has a 17-18-month breeding cycle on islands off the west coast of Western Australia. Buller, North Fisherman and Beagle Is are the main pupping sites, with several very small colonies (n> 3) at the Abrolhos Is. The 4-5-month pupping seasons are synchronised at North Fisherman and Beagle Is, but the sea-lions from Buller I. breed one month later and those from the Abrolhos Is two months earlier. Pup production and pup mortality were highly variable between seasons over which observations were recorded: 129 pups were born at the main breeding sites in early 1988, the mortality in the first five months was 7.1%, whereas 181 pups were born in late 1989 of which 24.3% died. Pups remain in the vicinity of their natal islands for the first 4-5 months of life before leaving, perhaps on foraging trips, with their mothers. Most return to their natal island, although others haulout on islands up to 27 km away. Some male N. cinerea congregate in bachelor colonies on islands adjacent to the Perth metropolitan region during the non-breeding season and migrate up to 280 km north each breeding season. The status of the isolated, west-coast N. cinerea population is unknown. The current high level of human pressure on sea-lion terrestrial habitats and their food resources indicate a need for further monitoring of this species.


2011 ◽  
Vol 59 (1) ◽  
pp. 54 ◽  
Author(s):  
Andrew D. Lowther ◽  
Simon D. Goldsworthy

Maternal strategies of otariid seals reflect the optimisation between resource exploitation and offspring provisioning driven across spatially separated foraging and nursing grounds. Intercolony variation in the expression of maternal strategies may represent temporal and spatial differences in resource availability, intraspecies competition or differences in life-history traits. The current study describes maternal strategies of the Australian sea lion at the largest breeding colony of the species (Dangerous Reef) and a comparative analysis was performed with data collected 16 years earlier at Seal Bay (Kangaroo Island). Significant differences in maternal strategies were characterised by lower milk lipid content (21.0 versus 28.9%), abbreviated periods onshore (0.93 versus 1.63 days) and slower pup growth rates (0.09–0.12 kg day–1) at Dangerous Reef. These data suggest flexibility in the expression of maternal investment between breeding sites and support the hypothesis of localised adaptation


2010 ◽  
Vol 58 (2) ◽  
pp. 94 ◽  
Author(s):  
Peter D. Shaughnessy ◽  
Jane McKenzie ◽  
Melanie L. Lancaster ◽  
Simon D. Goldsworthy ◽  
Terry E. Dennis

Australian fur seals (Arctocephalus pusillus doriferus) breed on Bass Strait islands in Victoria and Tasmania. They have been recorded in South Australia (SA) for many years as non-breeding visitors and on Kangaroo Island frequently since 1988, mostly in breeding colonies of the New Zealand fur seal (A. forsteri) which is the most numerous pinniped in SA. Australian fur seals have displaced New Zealand fur seals from sections of the Cape Gantheaume colony on Kangaroo Island. North Casuarina Island produced 29 Australian fur seal pups in February 2008. Australian fur seal pups were larger than New Zealand fur seal pups in the same colony and have been identified genetically using a 263-bp fragment of the mitochondrial DNA control region. North Casuarina Island has been an important breeding colony of New Zealand fur seals, but pup numbers there decreased since 1992–93 (contrary to trends in SA for New Zealand fur seals), while numbers of Australian fur seals there have increased. This study confirms that Australian fur seals breed in SA. The two fur seal species compete for space onshore at several sites. Australian fur seals may compete for food with endangered Australian sea lions (Neophoca cinerea) because both are bottom feeders.


2006 ◽  
Vol 33 (8) ◽  
pp. 661 ◽  
Author(s):  
Rebecca R. McIntosh ◽  
Brad Page ◽  
Simon D. Goldsworthy

Dietary remains recovered from Australian sea lion (Neophoca cinerea) digestive tracts and regurgitate samples from Seal Bay (Kangaroo Island, South Australia) were used to identify prey species consumed. Four of eight digestive tracts collected (50%) contained prey items located only in the stomach. On the basis of biomass reconstruction of cephalopod prey remains, octopus contributed 40% of the biomass in the samples, giant cuttlefish (Sepia apama) contributed 30% and ommastrephid squids contributed 14% biomass. The remains of several fish species were found in the samples: leatherjacket (Monocanthidae), flathead (Platycephalus sp.), swallowtail (Centroberyx lineatus), common bullseye (Pempheris multiradiata), southern school whiting (Sillago flindersi) and yellowtail mackerel (Trachurus novaezelandiae). Southern rock lobster (Jasus edwardsii) and swimming crab (Ovalipes australiensis) carapace fragments, little penguin (Eudyptula minor) feathers and bones and shark egg cases (oviparous species and Scyliorhinidae sp.) were also identified.


2009 ◽  
Vol 36 (2) ◽  
pp. 169 ◽  
Author(s):  
A. M. M. Baylis ◽  
D. J. Hamer ◽  
P. D. Nichols

Information on the diet of threatened species is important in devising appropriate management plans to ensure their conservation. The Australian sea lion (Neophoca cinerea) is Australia’s only endemic and globally one of the least numerous pinniped species. However, dietary information is currently limited because of the difficulty in using traditional methods (identification of prey hard parts from scats, regurgitates and stomach samples) to reliably provide dietary information. The present study assessed the use of fatty acid (FA) analysis to infer diet using milk samples collected from 11 satellite tracked Australian sea lions from Olive Island, South Australia. Satellite tracking revealed that females foraged in two distinct regions; ‘inshore’ regions characterised by shallow bathymetry (10.7 ± 4.8 m) and ‘offshore’ regions characterised by comparatively deep bathymetry (60.5 ± 13.4 m). Milk FA analysis indicated significant differences in the FA composition between females that foraged inshore compared with those that foraged offshore. The greatest differences in relative levels of individual FAs between the inshore and offshore groups were for 22 : 6n-3 (6.5 ± 1.2% compared with 16.5 ± 1.9% respectively), 20 : 4n-6 (6.1 ± 0.7 compared with 2.5 ± 0.7 respectively) and 22 : 4n-6 (2.4 ± 0.2% compared with 0.8 ± 0.2% respectively). Using discriminant scores, crustacean, cephalopod, fish and shark-dominated diets were differentiated. The discriminant scores from Australian sea lions that foraged inshore indicated a mixed fish and shark diet, whereas discriminant scores from Australian sea lions that foraged offshore indicated a fish-dominated diet, although results must be interpreted with caution due to the assumptions associated with the prey FA dataset. FA analysis in combination with satellite tracking proved to be a powerful tool for assessing broad-scale spatial dietary patterns.


2006 ◽  
Vol 28 (1) ◽  
pp. 65 ◽  
Author(s):  
J. K. Ling ◽  
C. Atkin ◽  
A. Barnes ◽  
A. Fischer ◽  
M. Guy ◽  
...  

Australian sea lions (Neophoca cinerea) are known to have been kept in aquaria and zoos in Australia since 1965. During that time at least 41 births were recorded, of which 19 were in Adelaide, 15 at Adelaide Zoo and 4 at Marineland of South Australia. The mean interval between successive births in Adelaide was 538.9 � 9.5 days (18.0 months; n = 10) and the mean assumed pregnancy period, including embryonic diapause, was 536.0 � 11.4 days (17.9 months; n = 9). The mean interval between parturition and presumed successful mating was 8.4 � 1.6 days (n = 5). Births occurred in all months except January, June, August and December. Figures for New South Wales and Queensland establishments are too small and scattered over time for any pregnancy periods or birth intervals to be determined. Likewise, latitudinal differences, if any, were not evident, because of the paucity of data from these more northerly places. One female at the Adelaide Zoo produced 8 pups between 1986 and 1997; she is still alive after 22 years in captivity. The youngest known-age (captive-born) female was 4 years, 8 months old when she gave birth to her first pup; and the oldest female in captivity to give birth to a pup was aged approximately 21 years, 8 months. The longest recorded captive period for a female was more than 25 years by 31 December 2003, and for a male it was 21 years, 11 months. A captive-bred female was still alive after 18 years, 2 months, 24 days; another such female died aged 18 years, 2 months, 18 days. These life spans appear to be similar to those that meagre data suggest for tagged N. cinerea in the wild.


2008 ◽  
Vol 86 (8) ◽  
pp. 826-833 ◽  
Author(s):  
P. Parker ◽  
J. T. Harvey ◽  
J. M. Maniscalco ◽  
S. Atkinson

Pupping-site fidelity (defined as pupping within 5.8 m of a previous location in ≥2 years) in Steller sea lions ( Eumetopias jubatus (Schreber, 1776)) was investigated during the breeding seasons from 2001 to 2005 at Chiswell Island, a small rookery in the Gulf of Alaska. Density of females was minimal with 54–80 pups born. Photo-identification of individuals and GPS points, including elevation of the rookery, were used to determine locations of 297 births. Sixty-four percentage (35/55) of the females exhibited pupping-site fidelity, and mean frequency of site fidelity was greater for females that gave birth >3 times. Fifty percentage of the births occurred at 22% of the locations for all years, indicating that multiple births occurred at some locations throughout the breeding season. Competition or aggression among females for specific pupping locations before birth was not observed, and there was no temporal order of pupping locations used, indicating that the rookery was not overcrowded and that many suitable pupping locations existed. Multiparous females gave birth at significantly greater distances from the surf zone than primiparous females. Long-term monitoring of pupping-site fidelity in combination with other measures of maternal care will ultimately determine which factors have the greatest effect on pup survival.


1991 ◽  
Vol 39 (3) ◽  
pp. 351 ◽  
Author(s):  
RA Tedman

This first account of the morphology of the female reproductive tract of the Australian sea lion, Neophoca cinerea, is based on examination of 15 specimens. The morphology of the female reproductive tract is similar in most respects to that in other pinniped species; only features peculiar to the species are described. The Y-shaped, bicornuate uterus is for the most part septate, but has a common uterine canal that is relatively much longer than that in other otariids. The uterine mucosa of newborns is slightly hypertrophied and regresses considerably by 3 weeks postpartum. During the embryonic diapause the uterine mucosa has serrated luminal epithelium, coiled uterine glands, and tall luminal and glandular epithelia. The mucosa of the adult vagina decreases in thickness from 100-mu-m at about 2 weeks postpartum to 20-mu-m 14.5 weeks postpartum, indicative of the regressive phase typical of the delay period in other pinnipeds. The urethral meatus lacks urinary papillae, unlike most other pinnipeds. A relatively large clitoris is present, and an os clitoridis was collected from one old individual. A monoestrous cycle seemed to occur in four animals, but a polyoestrous cycle is suspected in at least one individual. Ovulation occurs from alternate ovaries in successive pregnancies. Corpora albicantia are retained for at least three breeding seasons and probably longer. Implantation occurs in the midsection of the uterine cornu, ipsilateral to the ovary that released the egg. The maximum period of embryonic diapause cannot be ascertained from the available data, although a delay of about 8-9 months is possible if the breeding cycle (pregnancy cycle) lasts about 18 months.


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