Estimating pup production in a mammal with an extended and aseasonal breeding season, the Australian sea lion (Neophoca cinerea)

2012 ◽  
Vol 39 (2) ◽  
pp. 137 ◽  
Author(s):  
Rebecca R. McIntosh ◽  
Simon D. Goldsworthy ◽  
Peter D. Shaughnessy ◽  
Clarence W. Kennedy ◽  
Paul Burch

Context The Australian sea lion population at Seal Bay Conservation Park, South Australia, was estimated to be declining at a rate of 1.14% per breeding season, on the basis of maximum counts of live pups in each of 13 breeding seasons (Shaughnessy et al. 2006). The reliability of the pup-production estimates used to identify this decline is uncertain. Aims Our aims were to obtain representative and repeatable estimates of pup production and to assess the current rate of decline. Methods We compared four estimates of pup abundance over five breeding seasons (2002–03, 2004, 2005–06, 2007, 2008–09), including the count of cumulative new births, the maximum live-pup count, the number of pups given passive integrated transponder (PIT) tags, and mark–recapture methods using the Petersen estimate. Key results A total of 90% of pup births occurred over a mean of 124 days (s.d. = 14). Final estimates of pup production (from the largest of the four estimation methods used) in the five seasons were 227 (CL 221–239), 288 (CL 273–302), 219 (NA), 260 (CL 254–272) and 268 (CL 268–269). The average estimate of pup mortality was 28.6% (s.d. = 6.3%). The decline in the population at Seal Bay over 17 breeding seasons on the basis of maximum counts of live pups was 0.51% per year or 0.76% per breeding season. However, this trend was not based on best estimates of pup production. On the basis of final estimates for the last five breeding seasons, there is no declining trend. Conclusions The count of cumulative new births was the most reliable measure of pup production; the Petersen mark–recapture estimate provided a check for accuracy and confidence limits about the estimate. Implications The actual rate of change and the expected trajectory of the Seal Bay population remain uncertain. Ongoing monitoring is a priority for this site, using the reliable methods of estimating pup production identified in the present study.

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.


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


1995 ◽  
Vol 22 (2) ◽  
pp. 201 ◽  
Author(s):  
PD Shaughnessy ◽  
SD Goldsworthy ◽  
JA Libke

Kangaroo Island was an important seal-harvesting site during the early years of European colonisation of Australia. A recent survey of the New Zealand fur seal, Arctocephalus forsteri, in South and Western Australia indicates that Kangaroo I. is still an important centre for the species. In order to determine changes in the abundance of the population, numbers of pups were determined at four colonies on Kangaroo Island by mark-recapture in up to five breeding seasons from 1988-89 to 1992-93. Clipping was the preferred technique for mark-recapture estimation of pups because it was quick, easy and effective. Recaptures were conducted visually; they were repeated several times in each season to improve precision of the estimates. No pups were marked between recaptures in order to minimise disturbance. Assumptions made in estimating population size by the mark-recapture technique pertinent to this study are reviewed. Pup numbers increased at three colonies: at Cape Gantheaume, from 458 to 867 over five years (with exponential rate of increase r = 0.16, n = 5); at Nautilus North, from 182 to 376 over five years (at r = 0.19, n = 4); and at North Casuarina Islet, from 442 to 503 over four years (at r = 0.043, n = 2). Rates of increase in the first two colonies are similar to those at the most rapidly increasing fur seal populations in the Southern Hemisphere. The Kangaroo I. population is estimated to be 10000 animals in 1992-93. It is likely to be at the recolonisation phase of growth, with high rates of increase at individual colonies (or parts of colonies) resulting from local immigration. As space does not appear to be limiting expansion in these colonies, fur seal numbers may continue to increase there.


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.


2013 ◽  
Vol 35 (1) ◽  
pp. 93 ◽  
Author(s):  
Rebecca R. McIntosh ◽  
Clarence W. Kennedy

During a study of the demographics of the Australian sea lion (Neophoca cinerea), the sex ratio and morphology were obtained from 128 pups at Seal Bay Conservation Park over three breeding seasons (2002–03, 2004 and 2005–06). Gross necropsies were also performed. Dead pups were small and young, averaging 8.0 and 7.0 kg in weight, and 75.2 and 71.3 cm in length, for males and females respectively, only 1.8 kg heavier and 6.7 cm longer than newborn pups. There was no sex bias in the dead pups overall or in each cause of death classification. In 49% of mortalities, cause of death could not be inferred from gross necropsy and pups appeared in good condition. In pups in which cause of death was inferred, trauma inflicted by conspecifics was the primary result in both males and females (31.6%), followed by emaciation (10.4%), stillbirth or premature birth (7.6%) and possible shark attack (1.4%). Histopathological examination of tissues and other investigations would be required to determine whether other factors, such as disease or parasitic infection, and pollutant contamination contribute to pup mortality.


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.


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.


1999 ◽  
Vol 26 (1) ◽  
pp. 35 ◽  
Author(s):  
Nicholas J. Gales ◽  
David J. Fletcher

The abundance of the New Zealand sea lion, Phocarctos hookeri, was estimated using a model that incorporated estimated pup production. Pups are born at only five sites, four of which are at the sub-Antarctic Auckland Islands, which lie to the south of New Zealand. The remaining breeding site is at Campbell Island in the same region. Pup production was estimated during the 1994/95 and 1995/96 breeding seasons from mark–recapture studies at the two largest sea lion rookeries, at the Auckland Islands (Sandy Bay and Dundas Island), which account for almost 90% of total pup production for the species. Pup production for the other sites was estimated from direct counts or, in the case of Campbell Island, from recent tagging data. Total pup production estimates for all sites during the 1994/95 and 1995/96 breeding seasons are 2640 and 2807 respectively. During the four-week pupping season, pup mortality at most sites was estimated to be about 10%. The estimates of absolute abundance based on pup production for the two breeding seasons were 11 700 (95% confidence interval (CI): 10 500–13 100) and 12 500 (95% CI: 11 100–14 000) respectively. This population abundance is among the smallest reported for a species within the Otariidae. The highly localised, and historically reduced distribution make this species vulnerable to impact and warrants particular attention from conservation managers. In particular, the potential impact of the annual bycatch of P. hookeri in a trawl fishery requires close monitoring and, ideally, some mitigation action.


2007 ◽  
Vol 55 (5) ◽  
pp. 299 ◽  
Author(s):  
Darren G. Bos ◽  
Susan M. Carthew

The movement behaviour of a small dasyurid (Ningaui yvonneae) was investigated using mark–recapture data collected over 28 months from a population in the Middleback Ranges, South Australia. We were particularly interested in assessing variability in patterns of movement between the sexes and across seasons, as this has potentially important implications for population composition and dynamics. The species was found to be fairly mobile, with frequent and sometimes large movements relative to the size of the animal (up to 900+ m). Average distances moved between recaptures within and between trap sessions were 84 m and 160 m respectively, with nearly half of all recorded movements being between trapping grids (i.e. >80 m). Relatively high recapture rates (many separated by more than 100 days) and measures of site fidelity indicated that the species was not particularly transitory, but probably establishes large and/or drifting home ranges. However, patterns of movement varied considerably according to sex and the time of year. Female N. yvonneae were generally more sedentary than males, with few females moving between trapping grids, and most short-term movements (<100 days apart) being less than 70 m. Movements of females for which the records were separated by more than 100 days tended to be larger, with an average between-capture distance >200 m. In contrast, males often moved between trapping grids, even over short periods. Some short-term movements were more than 600 m in length, and the average distance moved within trapping sessions was >100 m. During the breeding season, males more than doubled the average distances moved between recaptures, when they were presumably roaming in search of females. For females, movement distances were similar during the prebreeding and breeding seasons, but were significantly smaller in the postbreeding season, when they were caring for young.


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