Niche overlap and habitat use at distinct temporal scales among the California sea lions(Zalophus californianus) and Guadalupe fur seals (Arctocephalus philippii townsendi)

2015 ◽  
Vol 32 (2) ◽  
pp. 466-489 ◽  
Author(s):  
Nereyda Pablo-Rodríguez ◽  
David Aurioles-Gamboa ◽  
Jorge L. Montero-Muñoz
1990 ◽  
Vol 68 (1) ◽  
pp. 150-158 ◽  
Author(s):  
George A. Antonelis ◽  
Brent S. Stewart ◽  
Wayne F. Perryman

The foraging characteristics of northern fur seals (Callorhinus ursinus) and California sea lions (Zalophus californianus) from San Miguel Island, California, were studied during the 1985 summer breeding season. A radio transmitter was attached to 25 postpartum females of each species and used to determine their locations at sea and the frequency and duration of their feeding trips. Northern fur seals usually foraged in the oceanic zone where the mean water depth was 933 m (n = 12). California sea lions principally were found in the neritic zone, where water depth averaged 323 m (n = 9). Most fur seals (92%) were found northwest of San Miguel Island, whereas the sea lions were commonly found to the northwest (55%) or in areas south (22%) of the island. Although both species evidently foraged at similar distances from the island, foraging trips of fur seals [Formula: see text] were over twice as long as those of sea lions [Formula: see text]. Fur seals were ashore less time [Formula: see text] than were sea lions [Formula: see text] between foraging trips. Analysis of scats revealed that fur seals and sea lions ate similar prey (northern anchovy, Engraulis mordax; Pacific whiting, Merluccius productus; juvenile rockfish, Sebastes spp.; market squid, Loligo opalescens; and nail squid, Onychoteuthis borealijaponicas), although the relative proportions of these prey differed. Factors influencing the observed foraging characteristics probably were availability of prey and phylogenetic constraints associated with life-history traits of northern fur seals and California sea lions.


2005 ◽  
Vol 5 (1) ◽  
pp. 140-142 ◽  
Author(s):  
F. D. HERNANDEZ-VELAZQUEZ ◽  
C. E. GALINDO-SANCHEZ ◽  
M. I. TAYLOR ◽  
J. DE LA ROSA-VELEZ ◽  
I. M. COTE ◽  
...  

2001 ◽  
Vol 79 (6) ◽  
pp. 1080-1087 ◽  
Author(s):  
Anthony J Orr ◽  
James T Harvey

The purpose of this study was to quantify the errors associated with using fecal samples to determine the diet of the California sea lion (Zalophus californianus). Fishes and squids of known size and number were fed to five sea lions held in enclosures with seawater-filled pools. Enclosures were washed and pools were drained periodically so that sea lion feces could be collected using a 0.5 mm mesh bag. Fish otoliths and squid beaks were collected from feces and used to estimate number and size of prey eaten. An average of 50.7% (SE = 6.4%) of 430 fishes and 73.5% (SE = 12.0%) of 49 cephalopods fed to sea lions were represented by otoliths and beaks in feces, respectively. Estimated lengths of fish from feces were less than lengths of fish fed to sea lions by an average of 30.1% (SE = 2.8%). Beaks were not digested significantly; estimated lengths of squid were underestimated by an average of only 3.3% (SE = 1.5%) relative to actual lengths. Passage rates of otoliths varied, but more than 70% were recovered within 48 h after the fish was consumed. Passage rates of beaks were generally less than those of otoliths; six beaks (11%) were collected in feces 4 days after the squid were eaten. Correction factors were created to more reliably estimate the number and size of fishes and cephalopods eaten by California sea lions.


2018 ◽  
Vol 54 (3) ◽  
pp. 581-586 ◽  
Author(s):  
Alissa C. Deming ◽  
Kathleen M. Colegrove ◽  
Padraig J. Duignan ◽  
Ailsa J. Hall ◽  
James F. X. Wellehan ◽  
...  

2011 ◽  
Vol 94 (3) ◽  
pp. 243-248 ◽  
Author(s):  
T Goldstein ◽  
KM Colegrove ◽  
M Hanson ◽  
FMD Gulland

2008 ◽  
Vol 39 (4) ◽  
pp. 542-547 ◽  
Author(s):  
Sophie Dennison ◽  
Martin Haulena ◽  
D. Colette Williams ◽  
John Dawson ◽  
Brian S. Yandell ◽  
...  

2005 ◽  
Vol 42 (2) ◽  
pp. 184-191 ◽  
Author(s):  
P. A. Silvagni ◽  
L. J. Lowenstine ◽  
T. Spraker ◽  
T. P. Lipscomb ◽  
F. M. D. Gulland

Over 100 free-ranging adult California sea lions ( Zalophus californianus) and one Northern fur seal ( Callorhinus ursinus), predominantly adult females, were intoxicated by domoic acid (DA) during three harmful algal blooms between 1998 and 2000 in central and northern California coastal waters. The vector prey item was Northern anchovy ( Engraulis mordax) and the primary DA-producing algal diatom was Psuedonitzschia australis. Postmortem examination revealed gross and histologic findings that were distinctive and aided in diagnosis. A total of 109 sea lions were examined, dying between 1 day and 10 months after admission to a marine mammal rehabilitation center. Persistent seizures with obtundation were the main clinical findings. Frequent gross findings in animals dying acutely consisted of piriform lobe malacia, myocardial pallor, bronchopneumonia, and complications related to pregnancy. Gross findings in animals dying months after intoxication included bilateral hippocampal atrophy. Histologic observations implicated limbic system seizure injury consistent with excitotoxin exposure. Peracutely, there was microvesicular hydropic degeneration within the neuropil of the hippocampus, amygdala, pyriform lobe, and other limbic structures. Acutely, there was ischemic neuronal necrosis, particularly apparent in the granular cells of the dentate gyrus and the pyramidal cells within the hippocampus cornu ammonis (CA) sectors CA4, CA3, and CA1. Dentate granular cell necrosis has not been reported in human or experimental animal DA toxicity and may be unique to sea lions. Chronically, there was gliosis, mild nonsuppurative inflammation, and loss of laminar organization in affected areas.


Sign in / Sign up

Export Citation Format

Share Document