The diet of itinerant male Hooker's sea lions, Phocarctos hookeri, at sub-Antarctic Macquarie Island

1999 ◽  
Vol 26 (6) ◽  
pp. 839 ◽  
Author(s):  
Clive R. McMahon ◽  
Dave Holley ◽  
Susan Robinson

Scats were collected from itinerant male Hooker's sea lions, Phocarctos hookeri, at Macquarie Island and the uneroded faunal remains used to assess the diet. Uneroded sagittal otoliths were used to identify teleost fish and to calculate fish size. Prey items included 14 taxa of teleost fish, cephalopods, gastropods, crustaceans and fur seals. Fish constituted the primary component of the diet. Prey species previously uncommon in the diet of seals and penguins around Macquarie Island were commonly eaten by Hooker's sea lions. The sub-Antarctic horse fish (Zanclorhynchus spinifer) and the Patagonian tooth fish (Dissostichus eleginoides) were the two most abundant species and occurred in 62.5% and 41.7% of all scats respectively. There were no age-specific and individual differences in the diet of sea lions. Seasonal variances in diet were absent. Small plastic fragments (diameter ∼1 mm) were found only in association with otoliths of Electrona subaspera. Some overlap was seen between the diet of itinerant male Hooker's sea lions and the commercial fisheries that currently operate around Macquarie Island.

2001 ◽  
Vol 28 (3) ◽  
pp. 291 ◽  
Author(s):  
Simon Childerhouse ◽  
Bruce Dix ◽  
Nick Gales

Scat and regurgitate samples (n = 206) from New Zealand sea lions (Phocarctos hookeri) were collected at the Auckland Islands between December 1994 and February 1997. Most (82%) samples were collected during three summer seasons while the remainder (18%) were collected during a single winter season. Thirty-three taxa were identified from 3523 prey items. The six most abundant prey species accounted for 90% of all prey items. The two most numerically abundant prey species, octopus (Enteroctopus zelandicus) and opalfish (Hemerocoetes species) made up almost 50% of total prey items. Other important prey species included lobster krill (Munida gregaria), hoki (Macruronus novaezelandiae), oblique-banded rattail (Coelorhynchus aspercephalus), and salps (Pyrosoma atlanticum). New Zealand fur seals (Arctocephalus forsteri) and seabirds were also identified in samples. New Zealand sea lions are generalist feeders utilising a wide variety of prey items, with fish comprising the most common taxa (59%) numerically and both cephalopods (21%) and crustacea (15%) forming lesser, but still important, parts of the diet. Prey taxa identified indicate that New Zealand sea lions are utilising a wide variety of benthic, demersal and pelagic species ranging from the inter-tidal zone to waters deeper than 300 m. New Zealand sea lions at the Auckland Islands target different prey species to New Zealand sea lions at other locations although they have broadly consistent prey types, with fish as the major taxa. There is only a small overlap of New Zealand sea lion prey species with commercially targeted species on the Auckland Islands Shelf in the months sampled.


Author(s):  
Hikaru Watanabe ◽  
Tsunemi Kubodera ◽  
Taro Ichii ◽  
Mitsuo Sakai ◽  
Masatoshi Moku ◽  
...  

Diet and sexual maturation were examined in the winter–spring cohort of the neon flying squid, Ommastrephes bartramii, during its southward migration through the Kuroshio–Oyashio transition region of the western North Pacific. The main prey items are micronektonic animals and small pelagic fish, which were abundantly distributed throughout the study area. Among the prey species, O. bartramii was dependent on the Japanese anchovy Engraulis japonicus, which also migrate from the northern to southern transition region during the winter, and the micronektonic squid Watasenia scintillans throughout the study period. Other common prey items were Gonatopsis borealis, Diaphus theta, and Ceratoscopelus warmingii from October to November or December, and Tarletonbeania taylori after December. These dietary changes can be explained by the difference in the seasonal north–south migration patterns of the predator and prey species. Male sexual maturation progressed throughout the season, and most individuals were fully mature in January. In contrast, most of the females were immature throughout the study period. The feeding strategy of the squid in relation to their seasonal north to south migration and sexual maturation was discussed.


2007 ◽  
Vol 43 (3) ◽  
pp. 461-474 ◽  
Author(s):  
A. Castinel ◽  
P. J. Duignan ◽  
W. E. Pomroy ◽  
N. López-Villalobos ◽  
N. J. Gibbs ◽  
...  

2011 ◽  
Vol 68 (10) ◽  
pp. 1732-1743 ◽  
Author(s):  
Jodie Kemp ◽  
Stephen E. Swearer ◽  
Gregory P. Jenkins ◽  
Simon Robertson

Fine-scale shape variation and the added effect of partial digestion often limits accurate identification of different teleost prey species in marine diet studies using otoliths. We evaluated the use of fine-scale shape and trace element variation in digested otoliths to identify fish prey species from the diet of predators. Fourier analysis of otolith shape revealed significant variation between red cod ( Pseudophycis bachus ) and bearded rock cod ( Pseudophycis barbata ) otoliths. Incorporating otoliths that had been consumed by Australian fur seals ( Arctocephalus pusillus doriferus ) into a Fourier analysis discriminant model identified 73% of otoliths as those of red cod and 27% as those of bearded rock cod. However, in vitro digestion of red cod and bearded rock cod otoliths resulted in incorrect classification of both cod species otoliths to varying degrees when using Fourier analysis shape descriptors. There was significant variation between red cod and bearded rock cod otolith core chemistry. Incorporating otoliths consumed by the seals into an otolith core chemistry discriminant model identified all otoliths as those of red cod. Using otolith core chemistry to identify prey species was found to be successful, and there is great potential for this technique to have wider applications in investigating ecosystem trophic interactions.


2020 ◽  
Vol 8 (1) ◽  
Author(s):  
Monique Ladds ◽  
David Rosen ◽  
Carling Gerlinsky ◽  
David Slip ◽  
Robert Harcourt

Abstract Physiology places constraints on an animal’s ability to forage and those unable to adapt to changing conditions may face increased challenges to reproduce and survive. As the global marine environment continues to change, small, air-breathing, endothermic marine predators such as otariids (fur seals and sea lions) and particularly females, who are constrained by central place foraging during breeding, may experience increased difficulties in successfully obtaining adequate food resources. We explored whether physiological limits of female otariids may be innately related to body morphology (fur seals vs sea lions) and/or dictate foraging strategies (epipelagic vs mesopelagic or benthic). We conducted a systematic review of the increased body of literature since the original reviews of Costa et al. (When does physiology limit the foraging behaviour of freely diving mammals? Int Congr Ser 2004;1275:359–366) and Arnould and Costa (Sea lions in drag, fur seals incognito: insights from the otariid deviants. In Sea Lions of the World Fairbanks. Alaska Sea Grant College Program, Alaska, USA, pp. 309–324, 2006) on behavioural (dive duration and depth) and physiological (total body oxygen stores and diving metabolic rates) parameters. We estimated calculated aerobic dive limit (cADL—estimated duration of aerobic dives) for species and used simulations to predict the proportion of dives that exceeded the cADL. We tested whether body morphology or foraging strategy was the primary predictor of these behavioural and physiological characteristics. We found that the foraging strategy compared to morphology was a better predictor of most parameters, including whether a species was more likely to exceed their cADL during a dive and the ratio of dive time to cADL. This suggests that benthic and mesopelagic divers are more likely to be foraging at their physiological capacity. For species operating near their physiological capacity (regularly exceeding their cADL), the ability to switch strategies is limited as the cost of foraging deeper and longer is disproportionally high, unless it is accompanied by physiological adaptations. It is proposed that some otariids may not have the ability to switch foraging strategies and so be unable adapt to a changing oceanic ecosystem.


Behaviour ◽  
1976 ◽  
Vol 56 (1-2) ◽  
pp. 44-67 ◽  
Author(s):  
Glenn Hausfater

Abstract1. A group of 32 yellow baboons (Papio cynocephalus) in the Masai-Amboseli National Park, Kenya, caught and ate 45 vertebrate prey items during 2519.19 hours of observation. 2. Eighty percent of the prey items were mammals and the most frequently eaten species were African hares (Lepus capensis), vervet monkeys (Cercopithecus aethiops) and neonate gazelle (Cazella granti and G. thomsoni) in that order. The details of predatory behavior for each prey species are described. 3. Rates of predation were significantly higher during the long dry season than during other months of the year, although no correlation was found between total monthly rainfall and monthly rates of predation. A lognormal model however provided a good fit to the monthly rate of predation data suggesting that the rate of predation by Amboseli baboons was affected by several factors that acted multiplicatively with respect to each other and were themselves related to rainfall or dryness. 4. A mean of 2.3 individuals fed directly from the carcass of each prey item. A mean of 3.5 individuals per prey item fed directly or indirectly, i.e., on scraps, from each carcass. In general, both the number of individuals who fed from each carcass and the duration of their feeding bouts was dependent upon the gross body size of the prey item. Adult males fed directly from the carcass of prey items for about three times more minutes than expected from their number in the group; other classes of individuals fed directly from prey carcasses for only one-fourth as many minutes as expected. In general, an adult male would be expected to feed on each category of vertebrate prey at least once per year, while individuals of all other age-sex classes would be expected to feed on most prey categories only once every two years. 5. The most frequent social behavior around prey items was agonistic bouts; no cooperation, simultaneous feeding or specific begging gestures were observed. 6. Estimates of the total number of prey killed annually by Amboseli baboons indicate that baboon predation probably has a negligible effect on prey populations other than vervet monkeys. 7. It is speculated that the need for vitamin B12 underlies baboon predatory behavior, and perhaps that of other primate species as well.


2016 ◽  
Vol 53 (6) ◽  
pp. 1241-1247 ◽  
Author(s):  
S. A. Michael ◽  
B. L. Chilvers ◽  
S. A. Hunter ◽  
P. Duignan ◽  
W. Roe

2000 ◽  
Vol 203 (23) ◽  
pp. 3655-3665 ◽  
Author(s):  
D.P. Costa ◽  
N.J. Gales

The New Zealand sea lion, Phocarctos hookeri, is the deepest- and longest-diving sea lion. We were interested in whether the diving ability of this animal was related to changes in its at-sea and diving metabolic rates. We measured the metabolic rate, water turnover and diving behavior of 12 lactating New Zealand sea lions at Sandy Bay, Enderby Island, Auckland Islands Group, New Zealand (50 degrees 30′S, 166 degrees 17′E), during January and February 1997 when their pups were between 1 and 2 months old. Metabolic rate (rate of CO(2) production) and water turnover were measured using the (18)O doubly-labeled water technique, and diving behavior was measured with time/depth recorders (TDRs). Mean total body water was 66.0+/−1.1 % (mean +/− s.d.) and mean rate of CO(2) production was 0. 835+/−0.114 ml g(−)(1)h(−)(1), which provides an estimated mass-specific field metabolic rate (FMR) of 5.47+/−0.75 W kg(−)(1). After correction for time on shore, the at-sea FMR was estimated to be 6.65+/−1.09 W kg(−)(1), a value 5.8 times the predicted standard metabolic rate of a terrestrial animal of equal size. The mean maximum dive depth was 353+/−164 m, with a mean diving depth of 124+/−36 m. The mean maximum dive duration was 8.3+/−1.7 min, with an average duration of 3.4+/−0.6 min. The deepest, 550 m, and longest, 11.5 min, dives were made by the largest animal (155 kg). Our results indicate that the deep and long-duration diving ability of New Zealand sea lions is not due to a decreased diving metabolic rate. Individual sea lions that performed deeper dives had lower FMRs, which may result from the use of energetically efficient burst-and-glide locomotion. There are differences in the foraging patterns of deep and shallow divers that may reflect differences in surface swimming, time spent on the surface and/or diet. Our data indicate that, although New Zealand sea lions have increased their O(2) storage capacity, they do not, or cannot, significantly reduce their at-sea metabolic rates and are therefore likely to be operating near their physiological maximum.


Sign in / Sign up

Export Citation Format

Share Document