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1 ated on free-ranging otariids (fur seals and sea lions).
2 ity to assess the prevalence of ZcAV in live sea lions.
3 losely related to those adapted to seals and sea lions.
4 pi were obtained from control and chronic DA sea lions.
5 his mixing zone region have been optimal for sea lions.
6  since the last common ancestor of seals and sea lions.
7 achea, bronchi, and lungs from 11 California sea lions, 2 Northern elephant seals, and 10 rhesus maca
8 ith thick myelin sheaths (elephant seal: 9%, sea lion: 7%) and thin myelin sheaths (elephant seal: 91
9 and thin myelin sheaths (elephant seal: 91%, sea lion: 93%).
10 the closely related isolates AAVrh.32.33 and sea lion AAV and (ii) selective blockade or removal of c
11 is the first description of coxiellosis in a sea lion and suggests that exposure to sea lions may be
12        Numerous mammalian species, including sea lions and fur animals, have been infected.
13 understand susceptibility of wild California sea lions and Northern elephant seals to influenza A vir
14  and a naturally occurring condition in wild sea lions and simultaneously advance general knowledge o
15 limate change will likely prevent California sea lions (and other marine mammals) from attaining thes
16 ction and animal movement in sympatric seal, sea lion, and sea otter species sampled in the North Pac
17                        Populations of seals, sea lions, and sea otters have sequentially collapsed ov
18 rvational and experimental studies of seals, sea lions, and walruses reveal elements of vocal develop
19                                      Because sea lions are dynamic foragers that rely on flexible nav
20                                   California sea lions are one of the major marine mammal species alo
21                                              Sea lions are susceptible to a wide variety of viruses,
22 f bio-inspired whiskers on a model head of a sea lion, as used in our previous studies.
23  sites in 48 healthy dolphins and 18 healthy sea lions, as well as those of adjacent seawater and oth
24                     Distributions of Steller sea lions at sea displayed self-similar fractal patterns
25 rmine if the spatial distribution of Steller sea lions at sea displayed similar scaling properties to
26 dent patterns in the distribution of Steller sea lions at sea or linkages with SST may have been appa
27 s indicate that the distributions of Steller sea lions at sea were more influenced by bathymetry than
28  northern anchovy (Engraulis mordax), and in sea lion body fluids.
29 rom 2000-2010 to estimate probabilities of a sea lion born in one DPS being seen within the range of
30  no prior data on structural connectivity in sea lion brains, with or without neuropathology.
31       We analyzed >22,000 sightings of 4,172 sea lions branded as pups in each DPS from 2000-2010 to
32 olphin, which evolved independently from the sea lion but displays similar feeding behavior, also has
33 d serum albumin concentration, but only in a sea lion colony exposed to anthropogenic environmental i
34  including music, come from Ronan, a trained sea lion [Cook et al., J.
35 ntibody concentration during early Galapagos sea lion development were higher in a colony exposed to
36 ived in Peru, triggering massive pelican and sea lion die-offs.
37 a lions previously exposed to DA (chronic DA sea lions) display hippocampal neuropathology similar to
38                                   Chronic DA sea lions displayed hippocampal neuron loss in patterns
39  for comparison with samples from California sea lions during unexplained disease outbreaks.
40 n an effort to find linkages between Steller sea lions (Eumetopias jubatus) and their environment, th
41 ion trends support the separation of Steller sea lions (Eumetopias jubatus) into a western distinct p
42 ghest prevalence and abundance in California sea lion feces.
43  This ELISA provides a tool for testing live sea lions for ZcAV exposure and is valuable for subseque
44                     Currently, the Galapagos sea lion (GSL, Zalophus wollebaeki) and Galapagos fur se
45        Previous behavioural research on live sea lions has shown that they are able to detect the dir
46          Herein the flow around a 3D printed sea lion head, with integrated whiskers of comparable ge
47                 Evolving with their seal and sea lion hosts, they have managed to tolerate hypoxia, h
48 at, contrary to predictions, male California sea lions increased rather than decreased their average
49  reported in the lungs of captive California sea lions involved in a mortality event.
50 us, hippocampal neuropathology of chronic DA sea lions is similar to that of human patients with temp
51                    Significantly, California sea lion isolates formed a unique group, providing evide
52  in a sea lion and suggests that exposure to sea lions may be a risk factor for contracting Q fever.
53  Dairy cattle, farmed mink or South American sea lions may have the potential to serve as new mammali
54 re deployed on 10 groups of juvenile Steller sea lions (n=52) at eight different locations within the
55 , we surveyed the fecal virome in California sea lions of different ages and health statuses.
56 e decline of the endangered New Zealand (NZ) sea lion (Phocarctos hookeri) is linked to latent levels
57       Additionally, distributions of Steller sea lion point patterns were examined with respect to me
58 ble persistence of L. interrogans within the sea lion population.
59           ZcAV is prevalent in stranded wild sea lion populations and results suggest that PCR assays
60                            We tested whether sea lions previously exposed to DA (chronic DA sea lions
61 n the brainstem, thalamus, and cortex in one sea lion pup and the external anatomy of the brain in a
62        However, 35% of the variability in NZ sea lion pup production is explained by latent by-catch,
63 x, we processed brain sections from seal and sea lion pups for Nissl substance, cytochrome oxidase, a
64 ity of bacteriophages was higher in unweaned sea lion pups than in juveniles and animals in rehabilit
65 viral species were shed by pups and juvenile sea lions, respectively.
66                             We find that the sea lion's impressive array of whiskers is matched by a
67 nality of the KIR and most likely led to the sea lion's loss of D0.
68                                         This sea lion's sensorimotor synchronization was precise, con
69 es of marine mammals and seabirds (dolphins, sea lions, sanderlings, pelicans and cormorants).
70                                   Pinnipeds (sea lions, seals, and walruses) are notable for many rea
71 ssay (ELISA) to detect antibodies to ZcAV in sea lion serum.
72 ates that give ample chance to escape from a sea lion-sized predator, but humpback whales could captu
73 th the northern elephant seal and California sea lion spend most of their lives at sea, but each also
74                                   A pregnant sea lion stranded in the State of Washington was found t
75 to the inactivation of Tas1r2, we found that sea lion Tas1r1 and Tas1r3 are also pseudogenized, consi
76 ed serum and lung samples (n = 96) from wild sea lions that stranded along the California coast were
77         We showed, in a large sample of wild sea lions, that spatial memory deficits are predicted by
78 r receptor function is not restricted to the sea lion: the bottlenose dolphin, which evolved independ
79                     Pinnipeds like seals and sea lions use their whiskers to hunt their prey in dark
80  dimension were calculated for each group of sea lions using a unit square box-counting method, where
81 nt capsid of Parkville virus, and San Miguel sea lion virus serotype 4 (SMSV4), which are representat
82                                          The sea lion visual cortex is located at the posterior side
83 on recovery of many pinniped species (seals, sea lions, walrus) is a conservation success.
84  to human patients, hippocampal sclerosis in sea lions was unilateral in 79% of cases, mossy fiber sp
85 f wild marine carnivore, three seals and one sea lion, we find that Ly49 and KIR are each represented
86 ained opportunistically postmortem from wild sea lions with and without chronic clinical signs of tox
87 eal (Mirounga angustirostris) and California sea lion (Zalophus californianus) are members of a diver
88  documented energy budgets of the California sea lion (Zalophus californianus), a consumer of these s
89 s of the top marine predator, the California sea lion (Zalophus californianus), which have been stead
90 reas of the nervous system of the California sea lion (Zalophus californianus).
91                     The endangered Galapagos sea lion (Zalophus wollebaeki) is threatened simultaneou
92                                   California sea lions (Zalophus californianus) are abundant human-si
93 ira interrogans serovar Pomona in California sea lions (Zalophus californianus) as a case study to il
94                          Over 400 California sea lions (Zalophus californianus) died and many others
95                  Hundreds of wild California sea lions (Zalophus californianus) exposed to the algal
96 interneuron and bouton numbers in California sea lions (Zalophus californianus) that naturally develo