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1 ed to those that largely consume flesh (i.e. lions).
2 on free-ranging otariids (fur seals and sea lions).
3 ral carnivore hosts, the bobcat and mountain lion.
4 monious with the evolutionary history of the lion.
5 nd cheetahs in their ability to coexist with lions.
6 ly related to those adapted to seals and sea lions.
7 ere obtained from control and chronic DA sea lions.
8 lar evolution of PLV in bobcats and mountain lions.
9 on are closer contemporaries to wild Barbary lions.
10 mixing zone region have been optimal for sea lions.
11 ce the last common ancestor of seals and sea lions.
12 inct FIV subtypes isolated from free-ranging lions.
13 V detected in other captive and free-ranging lions.
14 lates from free-ranging bobcats and mountain lions.
15 nosity increasing hunting success of African lions.
16 to assess the prevalence of ZcAV in live sea lions.
17 ent transmission to or peaks of infection in lions.
19 thick myelin sheaths (elephant seal: 9%, sea lion: 7%) and thin myelin sheaths (elephant seal: 91%, s
22 er, luminosity, observer effect) influencing lion abundance and probability of detection directly int
26 simple non-invasive technique for estimating lion age in populations lacking long-term records, and s
28 the ant is seemingly unable to grasp the ant lion and it is killed without being induced to spray.
29 he first description of coxiellosis in a sea lion and suggests that exposure to sea lions may be a ri
30 ng a long-term serological dataset of CDV in lions and domestic dogs from Tanzania's Serengeti ecosys
31 CCR2 and CCR5 genes that was fixed in Asian lions and found at low frequency in African lions (Panth
32 ously characterized populations of cheetahs, lions and pumas in recapitulating demographic history.
33 a naturally occurring condition in wild sea lions and simultaneously advance general knowledge of th
34 calculated as the likelihood of encountering lions and spotted hyaenas based on their cumulative dist
35 risks by positioning themselves further from lions and spotted hyaenas than predicted by a random dis
37 oyed on all known social groups of cheetahs, lions and spotted hyaenas within a 2700 km(2) study area
38 -adapted virus which is less fit in mountain lions and under intense selection pressure in the novel
41 ional and experimental studies of seals, sea lions, and walruses reveal elements of vocal development
42 tionships are highly symmetrical, and female lions are "free agents" who only contribute to communal
47 ons from models of reproductive skew, female lions are unable to control each other's reproduction be
49 es in 48 healthy dolphins and 18 healthy sea lions, as well as those of adjacent seawater and other h
52 e if the spatial distribution of Steller sea lions at sea displayed similar scaling properties to the
53 patterns in the distribution of Steller sea lions at sea or linkages with SST may have been apparent
54 dicate that the distributions of Steller sea lions at sea were more influenced by bathymetry than SST
57 eral recent studies that document fine-scale lion-avoidance by cheetahs, this study further highlight
58 es, dogs, coyotes, wolves, bobcats, mountain lions, bears, and birds (buzzards, eagles, hawks, ravens
59 cies transmission models, infection peaks in lions became more frequent and asynchronous from those i
63 2000-2010 to estimate probabilities of a sea lion born in one DPS being seen within the range of the
65 We analyzed >22,000 sightings of 4,172 sea lions branded as pups in each DPS from 2000-2010 to esti
66 in, which evolved independently from the sea lion but displays similar feeding behavior, also has all
67 n in three of six PLVA genomes from mountain lions, but we did not detect selection among 20 PLVA iso
69 t we have found that group living in African lions causes a complex response to long-term ecological
70 s, focusing on Felidae (domestic cat, tiger, lion, cheetah, and leopard), Hominidae, and Bovidae geno
72 rum albumin concentration, but only in a sea lion colony exposed to anthropogenic environmental impac
74 oximately 500 individuals are declining, but lion conservation is successful in southern Africa, in p
75 seasons by both male (56%) and female (33%) lions, contributing the most to lion dietary biomass.
78 extinction, wild dogs primarily occupied low lion density areas and apparently abandoned the long-ter
79 examine the role of social organization and lion density in shaping transmission pathways and tested
80 rast, cheetahs mostly utilized areas of high lion density, and the stability of the cheetah populatio
81 cess within the N-mixture model conditioning lion detectability on their group response to call-ins a
82 ody concentration during early Galapagos sea lion development were higher in a colony exposed to anth
86 000 years ago), saber-toothed cats, American lions, dire wolves, and coyotes competed for prey resour
87 ons previously exposed to DA (chronic DA sea lions) display hippocampal neuropathology similar to tha
91 effort to find linkages between Steller sea lions (Eumetopias jubatus) and their environment, the ob
92 trends support the separation of Steller sea lions (Eumetopias jubatus) into a western distinct popul
95 t had been received from the Central Florida Lions Eye Bank and stored in preservation medium (Optiso
96 Donor eyes (108 pairs) from the Minnesota Lions Eye Bank were cut circumferentially at the pars pl
97 plant Services, St Louis, Missouri; the Iowa Lions Eye Bank, Iowa City; and the Utah Lions Eye Bank,
98 Iowa Lions Eye Bank, Iowa City; and the Utah Lions Eye Bank, Salt Lake City) and selected were those
99 wet age-related macular degeneration at the Lions Eye Institute and the Sir Charles Gairdner Hospita
101 tern blot screening (domestic cat, puma, and lion FIV antigens) and PCR analysis to survey worldwide
103 ealed the opportunistic hunting behaviour of lions for prey as diverse as elephants and mice, with el
104 s ELISA provides a tool for testing live sea lions for ZcAV exposure and is valuable for subsequent s
106 otorious case, a coalition of two adult male lions from Tsavo, southern Kenya, cooperatively killed d
107 tions of Northwestern Mediterranean (Gulf of Lions: GoL) muscle hakes compared to its Northeastern At
111 commend separate regional assessments of the lion in the World Conservation Union (IUCN) Red List of
112 roup from six cheetahs in a U.S. zoo and two lions in a European circus, and the other group from a t
113 anzania, which has the largest population of lions in Africa, and find that they have killed more tha
114 one-half, while estimating a 37% chance that lions in East Africa also decline by one-half over two d
116 of kills (i.e. feeding locations) of African lions in Hwange National Park, Zimbabwe, a semi-arid Afr
117 ce presented for a much later persistence of lions in North Africa, including generations when sighti
119 because of the proliferation of reintroduced lions in small, fenced, intensively managed, and funded
121 and FIVPle subtype E (9899 bp) isolated from lions in the Okavango Delta in Botswana, both resemble F
123 anization of FIVPle subtype B (9891 bp) from lions in the Serengeti National Park in Tanzania and FIV
126 primarily limited by density dependence, but lions in unfenced reserves are highly sensitive to human
127 Population models indicate a 67% chance that lions in West and Central Africa decline by one-half, wh
129 lation indicates that neither high levels of lion-inflicted mortality nor behavioural avoidance infli
131 d to accommodate the introduction of Asiatic lions into the sanctuary (n = 24 individuals), and the o
133 hippocampal neuropathology of chronic DA sea lions is similar to that of human patients with temporal
139 These include the large African carnivores (lion, leopard, cheetah, and spotted hyena), where FIV is
142 a sea lion and suggests that exposure to sea lions may be a risk factor for contracting Q fever.
143 taneous chemical and scent identification of lion MF in its totality (urine + MF), 2) identify charac
146 eployed on 10 groups of juvenile Steller sea lions (n=52) at eight different locations within the Ale
148 oved postmortem and were sent to the Florida Lions Ocular Pathology Laboratory, where they were proce
151 he distance to the nearest (contemporaneous) lion or spotted hyaena, long-term risk, calculated as th
154 agement We used N-mixture models to estimate lion (Panthera leo) abundance from call-in and track sur
158 tic cat (Felis catus), puma (Puma concolor), lion (Panthera leo), leopard (Panthera pardus), and Pall
160 be affected by predation and competition by lions (Panthera leo) and spotted hyaenas (Crocuta crocut
161 immunodeficiency virus (FIVPle ) in African lions (Panthera leo) at multiple scales in the Serengeti
164 lions and found at low frequency in African lions (Panthera leo), suggesting that this domain may ha
165 so known as feline immunodeficiency virus of lion, Panthera leo [FIVPle]) is present in free-ranging
167 erns in secondary prey consumption by female lions partly based on prey ecology with browsers, such a
168 cline of the endangered New Zealand (NZ) sea lion (Phocarctos hookeri) is linked to latent levels of
169 Additionally, distributions of Steller sea lion point patterns were examined with respect to measur
172 iversity, suggesting that it has been in the lion population for some time and may be significantly h
176 ts highlight the vulnerability of very small lion populations and the significance of continued conse
177 und a striking geographical pattern: African lion populations are declining everywhere, except in fou
178 Ple]) is present in free-ranging and captive lion populations at a seroprevalence of up to 100%; howe
180 ivision of preexisting territories, regional lion populations did not expand until short-term conditi
187 loci and found that genetic diversity in SMM lions, prior to 2009, was lower than that for any popula
188 ), between bobcats (Lynx rufus) and mountain lions (Puma concolor) for a small number of animals in C
190 et the SMMs support a population of mountain lions (Puma concolor), a very rare example of a large ca
191 e brainstem, thalamus, and cortex in one sea lion pup and the external anatomy of the brain in a seco
192 However, 35% of the variability in NZ sea lion pup production is explained by latent by-catch, and
193 e processed brain sections from seal and sea lion pups for Nissl substance, cytochrome oxidase, and v
194 of bacteriophages was higher in unweaned sea lion pups than in juveniles and animals in rehabilitatio
196 etal extracts from P. x hortorum cv. Nittany Lion Red, which led to the isolation of a paralysis-indu
197 ive cover, regional populations of Serengeti lions remained stable for 10- to 20-year periods and onl
199 y of FIV-Ple in a free-ranging population of lions reveals a dynamic transmission of virus in a socia
204 A(A)R subunits responsible for mediating the lion's share of tonic inhibition in hippocampal neurons.
206 associated with double mutants of eli1 lit (lion's tail), a cell expansion mutant, indicated that th
207 ouncil of Australia, Richard Pearce Bequest, Lions Save Sight Foundation, Brian King Fellowship, and
208 to assess whether these notorious man-eating lions scavenged carcasses during their depredations.
211 una includes two machairodontine felids, the lion-sized Machairodus coloradensis and a smaller, jagua
213 he northern elephant seal and California sea lion spend most of their lives at sea, but each also spe
216 nto a lateralized, unambiguous target (e.g., lion-stripes-tiger) or diverged onto different meanings
217 an unambiguous, lexically associated target (LION-STRIPES-TIGER) or diverged onto different meanings
218 Across all FIVPle gene regions except env, lion subtypes B and E are monophyletic, and marginally m
220 s of CDV infection in dogs preceded those in lions, suggesting that spill-over from dogs was the main
221 In this study, we reassess whether African lions suppress populations of cheetahs and African wild
224 he inactivation of Tas1r2, we found that sea lion Tas1r1 and Tas1r3 are also pseudogenized, consisten
226 fically, we analysed the surface textures of lion teeth to assess whether these notorious man-eating
227 erum and lung samples (n = 96) from wild sea lions that stranded along the California coast were test
228 We showed, in a large sample of wild sea lions, that spatial memory deficits are predicted by the
230 ceptor function is not restricted to the sea lion: the bottlenose dolphin, which evolved independentl
231 s the approximately 100- to 130-kg marsupial lion, Thylacoleo carnifex, the world's most specialized
235 e we simulate the population consequences of lion trophy hunting using a spatially explicit, individu
239 ension were calculated for each group of sea lions using a unit square box-counting method, whereas i
240 apsid of Parkville virus, and San Miguel sea lion virus serotype 4 (SMSV4), which are representative
241 corneal tissues processed by technicians at Lions VisionGift for DMEK between October 2011 and May 2
243 oided areas where likelihood of encountering lions was high and changed their behaviours in risky are
244 human patients, hippocampal sclerosis in sea lions was unilateral in 79% of cases, mossy fiber sprout
245 ld marine carnivore, three seals and one sea lion, we find that Ly49 and KIR are each represented by
246 d opportunistically postmortem from wild sea lions with and without chronic clinical signs of toxic e
247 of PLVB reflects the highly mobile mountain lion, with diverse PLVB isolates cocirculating in some a
248 e FIV genes gag, pol-RT, and pol-RNase among lions within 13 prides to assess the occurrence of FIV i
249 (Mirounga angustirostris) and California sea lion (Zalophus californianus) are members of a diverse c
253 interrogans serovar Pomona in California sea lions (Zalophus californianus) as a case study to illust
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