ライフサイエンスコーパス: dolphin

1 8 PFPIA (cormorants and pike) and 6:6 PFPIA (dolphins).

2 e dolphin and 97 to 99% correct for a second dolphin.

3 eatures were likely to have been used by the dolphin.

4 functional, as exemplified by coelacanth and dolphin.

5 d cell counts and fibrinogen in free-ranging dolphins.

6 y with body size for both common and striped dolphins.

7 DNA in brain tissue samples from two striped dolphins.

8 ounts likely are important feeding areas for dolphins.

9 ats as well as between echolocating bats and dolphins.

10 ld measurements of free-ranging echolocating dolphins.

11 prevalence of H. cetorum infection in these dolphins.

12 direct and has led to equivocal results with dolphins.

13 sking social behaviour impairment in exposed dolphins.

14 d over time among female Indian River Lagoon dolphins.

15 ) decreased with time in Indian River Lagoon dolphins.

16 nised level of social complexity in humpback dolphins.

17 and chlorinated bipyrroles in the Brazilian dolphins.

18 n dolphins under human care and free-ranging dolphins.

19 otoreceptor complements, such as spiders and dolphins.

20 lasma, cord, breastmilk and infant plasma of DolPHIN-1 participants (NCT02245022) presenting with unt

21 In DolPHIN-1, HIV-infected treatment-naive pregnant women (

22 In this randomised, open-label trial, DolPHIN-2, we recruited pregnant women in South Africa a

23 ns under human care compared to free-ranging dolphins (64 +/- 16 vs. 47 +/- 12 mug/ml P < 0.05).

24 e estimated abundance at approximately 2,300 dolphins (95% CI = 1,247-4,214) over the approximately 2

25 t the surprising finding that the bottlenose dolphin, a toothed whale, is clustered with microbats in

26 y, we conducted an aerial survey to estimate dolphin abundance across the fishery.

27 We investigated the relationship between dolphin abundance and ENSO, Southern Annular Mode, austr

28 Dolphin abundance was lowest during winter 2009, when do

29 Linear models indicated that dolphin abundance was significantly affected by ENSO, an

30 DOLPHIN achieves the following: (i) resolution of probes

31 There was a strong diel pattern in dolphin acoustic occurrence and behaviour, with higher d

32 ur aging rate biomarkers among 34 individual dolphins aging from 10 y to up to 40 y old, we could ide

33 rmance was between 75 to 86% correct for one dolphin and 97 to 99% correct for a second dolphin.

34 hree minke whales, a fin whale, a bottlenose dolphin and a finless porpoise.

35 e number of feeding events observed for each dolphin and consequently the feeding time for each indiv

36 The dolphin and human subjects had a significant difference

37 The dolphin and human subjects had a significant difference

38 land was also found to be random in both the dolphin and human thyroid gland; however, the size of fo

39 In both dolphin and human thyroid glands, the size of the follic

40 Six animals (5 striped dolphins and 1 common dolphin) showed IHC and/or molecul

41 337 samples from 5 body sites in 48 healthy dolphins and 18 healthy sea lions, as well as those of a

42 toplasmic ratio of 4 Indo-Pacific bottlenose dolphins and 2 human thyroid glands.

43 and Atlantic bottlenose (Tursiops truncatus) dolphins and a beluga whale (Delphinapterus leucas).

44 ysis of over 850 samples from 105 bottlenose dolphins and associated prey items were analyzed for alg

45 Apart from humans and apes, dolphins and elephants are also known for such capacitie

46 er captive and wild species, such as otters, dolphins and ferrets, that form calcium oxalate, struvit

47 ted as toxin vectors during recent deaths of dolphins and manatees, respectively.

48 ntoceti cetaceans (toothed whales, including dolphins and orcas).

49 Viral outbreaks in dolphins and other Delphinoidea family members warrant i

50 ploration of these differences in bottlenose dolphins and other marine mammals may identify veiled pr

51 bers of the mammalian order Cetacea (whales, dolphins and porpoises) are obligate aquatic swimmers th

52 Odontocetes (toothed whales, dolphins and porpoises) hunt and navigate through dark a

53 erstanding of the feeding ecology of oceanic dolphins and provides new insights into the role of seam

54 s the highly plastic behaviour of bottlenose dolphins and shows a previously unreported behaviour tha

55 tives of manatees, and other marine mammals (dolphins and whales) contain sflt-1, indicating that it

56 acoustically identifiable delphinid (Risso's dolphin) and six of which are not yet identified.

57 This is the first report of PFPIAs in fish, dolphin, and bird plasma.

58 A survey of PFPIAs was conducted in fish, dolphins, and birds from various locations in North Amer

59 as been detected in wild Atlantic bottlenose dolphins, and captive orcas have been killed by West Nil

60 gression of responses to mirrors among apes, dolphins, and elephants.

61 Apes, dolphins, and even rats demonstrate some such abilities;

62 Among mammals, modern cetaceans (whales, dolphins, and porpoises) are unusual in the absence of h

63 The exception is Cetacea (whales, dolphins, and porpoises), in which DG size, convolution,

64 y low levels of brevetoxins measured in live dolphins, and those stranding in the absence of a K. bre

65 early complete skeleton of the extinct large dolphin Ankylorhiza tiedemani comb.

66 Male humpback dolphins appear to be using sponges for signalling purpo

67 The extent to which individual dolphins are able to maintain continuous vigilance throu

68 Because bottlenose dolphins are long-lived mammals that develop comorbiditi

69 r with their potential neurotoxic effects in dolphins are recommended.

70 Modern whales and dolphins are superbly adapted for marine life, with tail

71 Thus, dolphins are the only animals other than humans that hav

72 disease conditions observed in Barataria Bay dolphins are uncommon but consistent with petroleum hydr

73 h bacterial 16S ribosomal RNA sequences from dolphins are unique.

74 generate hypotheses that can be tested using dolphins as subjects.

75 again found in cetaceans such as whales and dolphins as well as in marsupials.

76 ence and severity than those in Sarasota Bay dolphins, as well as those previously reported in other

77 -recapture estimates yielded 226 (SE = 38.5) dolphins associating with one trawler and some individua

78 steners performed as well or better than the dolphin at discriminating objects, and they reported the

79 ic presence and foraging activity of oceanic dolphins at two seamounts (Condor and Gigante) in the Az

80 Without trend data or correction factors for dolphin availability, the impact of bycatch on this dolp

81 campal formation of the Atlantic white-sided dolphin (AWSD) with the view to understand similarities

82 RPL4 were the most stable HKGs in bottlenose dolphin blood.

83 samples including seawater, bird eggs, fish, dolphin blubber, and in the breast milk of humans that c

84 species:- striped dolphins (SDs), bottlenose dolphins (BNDs) and killer whales (KWs) had mean PCB lev

85 and to study changes in metabolic content of dolphin breath with regard to a variety of factors.

86 ong conspecifics, because captive bottlenose dolphins can be trained to use novel, learned signals to

87 Our results demonstrate that dolphins can continuously monitor their environment and

88 The results indicated that dolphins can detect broadband signals slightly better th

89 Some dolphins can exceed speeds of 50 km/h, a feat accomplish

90 Experimental studies demonstrated that dolphins can use learned signals referentially.

91 Whales and dolphins (Cetacea) have excellent social learning skills

92 ill remain nearly constant with range as the dolphin closes in on it.

93 bundance estimate for any Australian pelagic dolphin community and documents individuals associating

94 circulating blood proteome of the bottlenose dolphin compared to terrestrial mammals and exploration

95 ELISA can be determined by testing sera from dolphins confirmed to be uninfected, PCR and Southern bl

96 Acoustic data demonstrate that small dolphins consistently use Condor and Gigante seamounts t

97 In contrast, sharks and dolphins contend with wall turbulence, are fast swimmers

98 The overall results establish that these dolphins could identify, through indicative cues alone,

99 accumulative contaminants in Atlantic common dolphin ( Delphinus delphis ) blubber, including compoun

100 ocoena phocoena) and one short-beaked common dolphin (Delphinus delphis) and in one 'dubious tattoo'

101 stranding event (MSE) of short-beaked common dolphins (Delphinus delphis) occurred in Falmouth Bay, C

102 Studies on wild dolphins demonstrated how this skill appears to be usefu

103 Bottlenose dolphins develop their own unique identity signal, the s

104 The results indicate that the dolphin did not appear to use overall echo amplitude, bu

105 In 1999/2000, 152 dolphins died following extensive K. brevis blooms and b

106 In 2004, 105 bottlenose dolphins died in the absence of an identifiable K. brevi

107 In 2005/2006, 90 bottlenose dolphins died that were initially coincident with high d

108 At least 26 dolphins died, and a similar number was refloated/herded

109 nvolved in events in which many manatees and dolphins died, but this has usually not been verified ow

110 Here we show that dolphins do possess an automatic gain control mechanism,

111 The current understanding of dolphin echolocation indicates that automatic gain contr

112 We find that the amplitude of the dolphins' echolocation signals are highly range dependen

113 Among mammals, this has been reported for dolphins, elephants, harbor seals, and humans.

114 e process" where a group of normally pelagic dolphins entered Falmouth Bay and, after 3-4 days in/aro

115 Of 29 dolphins evaluated from Barataria Bay, 48% were given a

116 logical handedness and homing correlate, and dolphins exhibit handedness in their listening response.

117 nstrate that, in a manner similar to humans, dolphins exhibit independent and linear age-related decl

118 The dolphins exhibited a significant post-respiratory tachyc

119 dic grid cells to emerge in bats, or perhaps dolphins, exploring a three-dimensional environment?

120 e in the chance of behavioural changes among dolphins exposed to anthropopressure (fishing activity),

121 This study demonstrates that bottlenose dolphins extract identity information from signature whi

122 appropriate method and test it to show that dolphins extract object characteristics directly from ec

123 e model to investigate changes in bottlenose dolphin fecundity and calf survival.

124 g ability is maintained throughout life, and dolphins frequently copy each other's whistles in the wi

125 es effective prediction of concentrations in dolphins from fish contaminant surveys which are logisti

126 he highest concentration was observed in the dolphins from Rio Grande do Sul (42% frequency of detect

127 weight [wet wt]) in the livers of bottlenose dolphins from Sarasota Bay, FL.

128 We analyzed mitochondrial DNA data from 94 dolphins from the coasts of South Africa, Mozambique, Ta

129 Analysis of the bottlenose dolphin genome revealed two full-length proviral sequenc

130 se dolphin (Tursiops truncatus), the Risso's dolphin (Grampus griseus), and the beluga whale (Delphin

131 of a freshwater apex predator, Ganges River dolphin (GRD, Platanista gangetica gangetica), which pla

132 uencing of a less-well-studied environment - dolphin gums - uncovers surprising novelty in the bacter

133 l loss of up to 80% of suitable white-beaked dolphin habitat.

134 bundance was lowest during winter 2009, when dolphins had high temporary emigration rates out of the

135 Dolphins harbour 30 bacterial phyla, with 25 of them in

136 prestin amino-acid sequences of echolocating dolphins have converged to resemble those of distantly r

137 y for denitrification and a possible role in dolphin health.

138 To evaluate potential sublethal effects on dolphins, health assessments were conducted in Barataria

139 ansmission pathways of foraging behaviors in dolphins, highlighting the similarities between cetacean

140 ling activity of the ZPA, is absent from the dolphin hind-limb bud.

141 ), and new US coding sequences were found in dolphins, horses, dogs, and cats.

142 led, 25-y longitudinal cohort of 144 US Navy dolphins housed in the same oceanic environment.

143 the globally Vulnerable Australian humpback dolphin in northern Ningaloo Marine Park (NMP), north-we

144 genetically isolated populations of humpback dolphins in areas that are environmentally distinct.

145 marine wildlife, including common bottlenose dolphins in sensitive coastal habitats.

146 Dolphins in the genus Delphinus provide a useful test ca

147 us and subcutaneous infections in humans and dolphins in the New World tropics.

148 spongers) are culturally distinct from other dolphins in the population based on the criteria that sp

149 ential environmental influences for humpback dolphins in the Western Indian Ocean.

150 ging strategy, "shelling" [17], whereby some dolphins in this population feed on prey trapped inside

151 ture hippopotamus GH is identical to that of dolphin, in accord with current ideas of a close relatio

152 ion on charismatic large vertebrates such as dolphins is often supported by the suggestion that these

153 ia lineage is found in both managed and wild dolphins; its metabolic profile suggests a capacity for

154 escribed as deletion-of-loop Asp-Phe-Gly-in (DOLPHIN) kinase models, demonstrate exceptional performa

155 h of two wild, stranded Atlantic white-sided dolphins (Lagenorhynchus acutus) and from the feces of t

156 red from the stomach of Atlantic white-sided dolphins (Lagenorhynchus acutus) and the feces of Pacifi

157 ree captive cetaceans (a Pacific white-sided dolphin [Lagenorhynchus obliquidens]; an Atlantic bottle

158 ether, these results suggest that bottlenose dolphin leaders have the opportunity to gain indirect be

159 ed during routine blood draws throughout the dolphins' lifetimes.

160 three sessions, each lasting five days, two dolphins maintained echolocation behaviors while success

161 For example, a dolphin may store 'sound templates' in its brain and ide

162 Here we show that dolphins may continuously echolocate and accurately repo

163 This implies that the tool-using dolphins may have been somewhat buffered against the cas

164 In horses, elephants, hyenas, dolphins, monkeys, and chimpanzees, some individuals for

165 o detect antibodies against the related pair dolphin morbillivirus and porpoise morbillivirus.

166 causative agent involved in these bottlenose dolphin mortality events.

167 In dolphins, natural selection has developed unihemispheric

168 estrial mammals, killer-whale and bottlenose-dolphin neonates and their mothers show little or no typ

169 the food chain, affecting many behaviors of dolphins observed at dusk including their depth, group s

170 Areas of high probability (> 0.6) of dolphin occurrence were primarily (90%) in multiple use

171 We described patterns of dolphins' occurrence using circular statistics and then

172 marine ecosystem dominated by porpoises and dolphins once this basin was reconnected back to the Med

173 Five lactating adult dolphins, one immature male, and one immature female tes

174 last-sighting records for the Yangtze River dolphin or baiji and two formerly economically important

175 Monitoring the status of river dolphins or other megafauna therefore has the potential

176 tor's genome before the divergence of modern dolphins or that an exogenous variant existed following

177 ey, resulting in the temporary emigration of dolphins out of the study area in search of adequate pre

178 into the salient features, the authors had a dolphin perform a match-to-sample task and then presente

179 In Experiment 1, the dolphins Phoenix and Akeakamai processed the identity of

180 Concurrently, we carried out boat-based dolphin photo-identification to assess short-term fideli

181 n PIV-3 (HPIV-3), bovine PIV-3 (BPIV-3), and dolphin PIV-1 (Tursiops truncatus PIV-1, or TtPIV-1).

182 cology of a small cetacean, the Ganges River dolphin (Platanista gangetica gangetica, GRD), in a larg

183 screen agents in tissue liver of Franciscana dolphin (Pontoporia blainvillei), a species under specia

184 ata, this small (<200 individuals), resident dolphin population has been extensively studied for over

185 predict PCB concentrations in the bottlenose dolphin population of Charleston, SC, USA, was developed

186 This study shows that Chilean dolphin population structure is consistent with predicti

187 availability, the impact of bycatch on this dolphin population's conservation status remains unknown

188 l as those previously reported in other wild dolphin populations.

189 logeny that places Cetacea (that is, whales, dolphins, porpoises) as the sister group to the extinct

190 In contrast, two bat species and dolphin possess no functional V1Rs, only pseudogenes, an

191 thers who share their subculture, tool-using dolphins prefer others like themselves, strongly suggest

192 as the most important variables influencing dolphin presence, with dolphins showing a preference for

193 itions may have affected the distribution of dolphin prey, resulting in the temporary emigration of d

194 During echolocation, dolphin produce clicks and listen to returning echoes to

195 rophone placed on the ventral midline of the dolphin produced a continuous heartbeat signal while the

196 The IB model for PCBs in bottlenose dolphins provides a novel approach to estimating the max

197 In bottlenose dolphins, remarkable small-scale differences in haplotyp

198 nd diverse radiation of delphinid cetaceans (dolphins) represents a good example of this.

199 Here, we show that wild bottlenose dolphins respond to hearing a copy of their own signatur

200 A 15-day testing session with one dolphin resulted in near perfect performance with no sig

201 Alternatively, a dolphin's brain may contain algorithms, derived through

202 is study provides compelling evidence that a dolphin's learned identity signal is used as a label whe

203 ith echoes from the same objects used in the dolphin's task.

204 cetorum were compared for 20 wild bottlenose dolphins sampled as part of a long-term health study.

205 Dolphins sampled in Barataria Bay showed evidence of hyp

206 of the franciscana (Pontoporia blainvillei) dolphin samples, whereas the frequency of detection decr

207 taceans, three out of four species:- striped dolphins (SDs), bottlenose dolphins (BNDs) and killer wh

208 Dolphin serum Vanin-1 ranged between 31-106 mug/ml, whic

209 ry of 11 proteins that appeared exclusive to dolphin serum.

210 This seems to be true for dolphins, sharks and bony fish, which swim at 0.2 < St <

211 ults suggest that an echolocating bottlenose dolphin should be able to detect a 7.62-cm diameter wate

212 The dolphin showed clinical signs of tachypnea, transient dy

213 Six animals (5 striped dolphins and 1 common dolphin) showed IHC and/or molecular evidence of morbill

214 variables influencing dolphin presence, with dolphins showing a preference for shallow waters (5-15 m

215 A new study of contact calls in dolphins shows that individuals can recognize one anothe

216 ud patterns, despite the fact that shark and dolphin skins are major targets of reverse engineering m

217 offshore wind farms and the Taiwanese white dolphin (Sousa chinensis taiwanensis) as an example.

218 idespread populations of Australian humpback dolphins (Sousa sahulensis) over ten years of observatio

219 potential sources of these chemicals in this dolphin species.

220 However, dolphins spent a significantly higher percentage of thei

221 was demonstrated in tattoos from one striped dolphin (Stenella coeruleoalba), eight harbour porpoises

222 Dolphin stomach contents frequently consisted of breveto

223 we investigate whether Shark Bay bottlenose dolphins that use marine sponges as hunting tools (spong

224 2% post-heatwave declines in the survival of dolphins that use tools to forage and those that do not,

225 ctral and diffuse Imaging in Near-infrared" (DOLPHIN), that resolves these challenges.

226 In dolphins, the bud arrests and degenerates around the fif

227 Bottlenose dolphins therefore appear to be unique as nonhuman mamma

228 The mean N/C ratio of the dolphin thyroid follicular epithelia and human follicula

229 The mean colloid volume of the dolphin thyroid gland and human thyroid gland was 1.22x1

230 lication of PUS for quantitative analyses of dolphin thyroid gland in both research and clinical prac

231 rease as a function of increasing age in the dolphin thyroid gland.

232 greement between the two ultrasound units in dolphin thyroid measurements (ICC = 0.859-0.976).

233 his information contributes to understanding dolphin thyroid physiology and its structural adaptation

234 ariability was found between PUS and FCUS in dolphin thyroid size measurements under identical scanni

235 evaluated the inter-equipment variability in dolphin thyroid ultrasound measurements between a portab

236 g to characterize the response of bottlenose dolphins to intense storms offshore Maryland, USA betwee

237 This allows dolphins to maintain consciousness in response to respir

238 Unihemispheric sleep may also allow dolphins to maintain vigilant states over long periods o

239 that the adaptation mechanisms of sharks and dolphins to their fluid environment have much in common.

240 al impacts of HOC exposure in two bottlenose dolphin ( Tursiops truncatus) ecotypes in the SCB.

241 ing behaviors in the Indo-Pacific bottlenose dolphin (Tursiops aduncus) population of Shark Bay, West

242 emporary emigration of a resident bottlenose dolphin (Tursiops aduncus) population off Bunbury, Weste

243 Shark Bay's resident Indo-Pacific bottlenose dolphin (Tursiops aduncus) population revealed a signifi

244 earing sensitivity of an Atlantic bottlenose dolphin (Tursiops truncatus) to both pure tones and broa

245 vestigate the cardiac responses of a captive dolphin (Tursiops truncatus) to sound playback stimuli.

246 ), griffon vulture (Gyps fulvus), bottlenose dolphin (Tursiops truncatus), American flamingo (Phoenic

247 small odontocetes, including the bottlenose dolphin (Tursiops truncatus), the Risso's dolphin (Gramp

248 d systematics, except for some exceptions in Dolphin (Tursiops truncatus).

249 ns var. gattii in a male Atlantic bottlenose dolphin (Tursiops truncatus).

250 udied populations of Indo-Pacific bottlenose dolphins (Tursiops aduncus) in south-western (SW) and Sh

251 a limited number of free-ranging bottlenose dolphins (Tursiops aduncus).

252 hark Bay, Western Australia, male bottlenose dolphins (Tursiops sp.) cooperate in pairs and triplets

253 Populations of bottlenose dolphins (Tursiops spp.) vary in male alliance formation

254 pleted serum proteins from common bottlenose dolphins (Tursiops truncatus) and pooled normal human se

255 iour and flipper accelerations of bottlenose dolphins (Tursiops truncatus) and Weddell seals (Leptony

256 Bottlenose dolphins (Tursiops truncatus) are a promising animal for

257 Bottlenose dolphins (Tursiops truncatus) develop individually disti

258 Echolocating bottlenose dolphins (Tursiops truncatus) discriminate between objec

259 ence genes in blood leukocytes of bottlenose dolphins (Tursiops truncatus) for gene transcription res

260 The authors tested 2 bottlenosed dolphins (Tursiops truncatus) for their understanding of

261 the Great Lakes in 2010-2012, and bottlenose dolphins (Tursiops truncatus) from Sarasota Bay, FL and

262 In the Florida Panhandle region, bottlenose dolphins (Tursiops truncatus) have been highly susceptib

263 analysis of blubber from 8 common bottlenose dolphins (Tursiops truncatus) inhabiting the Southern Ca

264 substances (PFAS) in free-ranging bottlenose dolphins (Tursiops truncatus) inhabiting two geographic

265 ments of the impact of bycatch on bottlenose dolphins (Tursiops truncatus) interacting with an Austra

266 authors tested whether the understanding by dolphins (Tursiops truncatus) of human pointing and head

267 ubber from two ecotypes of common bottlenose dolphins (Tursiops truncatus) sampled in the Southern Ca

268 stern Atlantic Ocean, tissue from bottlenose dolphins (Tursiops truncatus) stranded or incidentally c

269 een documented in a population of bottlenose dolphins (Tursiops truncatus) where direct benefits to l

270 diel cycles on the occurrence of bottlenose dolphins (Tursiops truncatus) within a Marine Protected

271 After the recent discovery of MSR in dolphins (Tursiops truncatus), elephants thus were the n

272 cetaceans, specifically Atlantic bottlenose dolphins (Tursiops truncatus).

273 n the oral gingival sulcus of two bottlenose dolphins (Tursiops truncatus).

274 g recovery from apnea in 11 adult bottlenose dolphins (Tursiops truncatus, 9 males and 2 females, bod

275 hynchus obliquidens]; an Atlantic bottlenose dolphin [Tursiops truncatus]; and a beluga whale [Delphi

276 Between 1999 and 2006, three bottlenose dolphin UMEs occurred in the Florida Panhandle region.

277 tified using parallel reaction monitoring in dolphins under human care and free-ranging dolphins.

278 Serum Vanin-1 was also higher in dolphins under human care compared to free-ranging dolph

279 the relatively poor visibility in the ocean, dolphins use echolocation to interrogate their environme

280 DOLPHIN was a phase 1/2, single-arm trial done at The Au

281 eported that the drag power experienced by a dolphin was larger than the estimated muscle power - thi

282 or convergence among bats and the bottlenose dolphin was seen in numerous genes linked to hearing or

283 uced a continuous heartbeat signal while the dolphin was submerged.

284 A dolphin watched a human informant either gazing at or po

285 ions between measures obtained on individual dolphins, we demonstrate that, in a manner similar to hu

286 The error patterns of the humans and the dolphin were compared to determine which acoustic featur

287 ions predicted in male and female bottlenose dolphin were in good agreement with observed tissue conc

288 ray calls) were recorded in >87% of the days dolphin were present.

289 Barataria Bay dolphins were 5 times more likely to have moderate-sever

290 During and following four autumnal storms, dolphins were detected less frequently and for shorter p

291 Two dolphins were exposed to reflective surfaces, and both d

292 On necropsy, all dolphins were in good nutritive status with empty stomac

293 Dolphins were present year round and nearly every day at

294 The isolates from the wild, stranded dolphins were sensitive to nalidixic acid, whereas the i

295 Disease conditions in Barataria Bay dolphins were significantly greater in prevalence and se

296 Dolphins were temporarily captured, received a veterinar

297 ve blood samples collected from 7 bottlenose dolphins were used to analyze 15 candidate HKGs (ACTB, B

298 t restricted to the sea lion: the bottlenose dolphin, which evolved independently from the sea lion b

299 In echolocating dolphins, which are studied as models for object recogni

300 erformed on 15 apparently healthy bottlenose dolphins with both PUS and FCUS under identical scanning