ライフサイエンスコーパス: cetacean

1 in, and pons of the minke whale, a mysticete cetacean.

2 we examined allelic variants of the MC4R in cetaceans.

3 etrapods, comparable in diversity to today's cetaceans.

4 on of noise-induced hearing loss in stranded cetaceans.

5 ochondrial mutation rates that are common to cetaceans.

6 reat apes, elephants, and some large-brained cetaceans.

7 ase states and breath metabolite profiles in cetaceans.

8 pigs and peccaries (that is, Suina) than to cetaceans.

9 r than phylogenetically derived estimates in cetaceans.

10 ry (asymmetrical SWS or ASWS) as observed in cetaceans.

11 resembling the unihemispheric slow waves of cetaceans.

12 he fin whale genome and analysed FGFs from 8 cetaceans.

13 t alternative mechanisms may have evolved in cetaceans.

14 ociated with gastritis and clinical signs in cetaceans.

15 velopment of gastric ulcers and gastritis of cetaceans.

16 can be obtained for physically unrestrained cetaceans.

17 wide variety of animal taxa, from insects to cetaceans.

18 mpling for remotely assessing health of wild cetaceans.

19 k mobility as suggested for rhinoceroses and cetaceans.

20 hus implicating FGF23 in low bone density in cetaceans.

21 al sleep phenomenology present in odontocete cetaceans.

22 one of the most important viral pathogens in cetaceans.

23 closest extant terrestrial relatives of the cetaceans.

24 n the suppression of REM sleep in odontocete cetaceans.

25 n the peripheral blood leukocytes in captive cetaceans.

26 r of animal species ranging from primates to cetaceans.

27 ng ecology, energy balance, and body size in cetaceans.

28 a large clade of carnivores, ungulates, and cetaceans.

29 th indicatora potential health indicator for cetaceans.

30 titors and potential predators of many other cetaceans.

31 [3] and in the vocal and feeding behavior of cetaceans [4, 5].

32 ize, paralleling the evolutionary history of cetaceans [7].

33 acutus) and from the feces of three captive cetaceans (a Pacific white-sided dolphin [Lagenorhynchus

34 Cetaceans, a group of mammals adapted to the aquatic env

35 Modern cetaceans, a poster child of evolution, play an importan

36 nter (NOAA) conducted six ship line-transect cetacean abundance surveys in the California Current off

37 ide novel insights into the roles of FGFs in cetacean adaptation to the aquatic environment.

38 mation about a possible pathogenic branch of cetacean alphaherpesviruses that might be responsible fo

39 concentration-response experiments with PB, cetacean and seal spp. immune cells to evaluate the effe

40 for the first time in southwestern Atlantic cetaceans and in contrast to North American marine mamma

41 n phylogeography and demographic history for cetaceans and other vertebrates, despite great uncertain

42 To determine how cetaceans and pinnipeds accomplish deep-sea chases, we d

43 ift-generating flipper-stroke for propulsion cetaceans and provides an additional function for the un

44 ong vertebrates, only microchiropteran bats, cetaceans and some rodents are known to produce and dete

45 lated to the recent massive killing of small cetaceans and to the continuing incidental catches in co

46 oceti: Phocoenidae) are some of the smallest cetaceans and usually feed near the seafloor on small fi

47 enetically distant taxa, the two-toed sloth, cetaceans, and higher primates.

48 Although songbirds, some cetaceans, and maybe bats may also be vocal learners, vo

49 240, 454, 800, and 7650 nM for birds, fish, cetaceans, and other mammals, respectively.

50 We sequenced the MC4R from 20 cetaceans, and pharmacologically characterized 17 of the

51 ning species (such as humans and some birds, cetaceans, and pinnipeds, but not nonhuman primates) are

52 s, parakeets, hummingbirds, bats, elephants, cetaceans, and primates.

53 ca) can be potential predators of many other cetaceans, and the interception of their vocalizations b

54 d near the origin of the modern suborders of cetaceans approximately 34 million years ago.

55 ms such as cichlids, coelacanths, seals, and cetaceans are active in UV-blue color environments, but

56 Extant cetaceans are found to be unique in that their canal arc

57 the aquatic adaptations in hippopotamids and cetaceans are inherited from their common ancestor.

58 Our cladistic analysis indicates that cetaceans are more closely related to artiodactyls than

59 Cetaceans are not the sister group to (any) mesonychians

60 The cetaceans are one of the few mammalian clades capable of

61 and the suppression of REM in the odontocete cetaceans are present in the minke whale.

62 Cetaceans are protected worldwide but vulnerable to inci

63 ) the remaining orders of placental mammals (cetaceans, artiodactyls, perissodactyls, carnivores, pan

64 egacy of noise overexposure in mass stranded cetaceans as a key to understanding the complex processe

65 n serve as an indication of health status in cetaceans as it occurs prior to alterations in hematolog

66 between brain mass and GI was evident in the cetaceans as seen in other mammals, with all cetaceans s

67 cardiac responses to acoustic stimuli from a cetacean at depth.

68 pregnant females in several species of wild cetaceans: Balaenapteraacutorostrata , Delphinusdelphis

69 on of these interactions and their effect on cetaceans' behavior.

70 ch the fast body rotations that characterize cetacean behaviour.

71 ce of research on the socio-cultural side of cetacean biology.

72 Cetacean body structure and physiology exhibit dramatic

73 has been linked to demethylation of MeHg in cetaceans, but its role in attenuating Hg toxicity in be

74 Health assessments of wild cetaceans can be challenging due to the difficulty of ga

75 One of the areas in which cetaceans can be compared with primates is that of objec

76 In cetaceans' communities, interactions between individuals

77 me echolocating bat species and echolocating cetaceans, contrasting with purifying selection on non-e

78 gas-forming disease afflicting some stranded cetaceans could be a type of decompression sickness (DCS

79 graphic data of variables known to influence cetacean dispersal and population structure.

80 m insights into what factors have influenced cetacean diversity in the past.

81 he recent and diverse radiation of delphinid cetaceans (dolphins) represents a good example of this.

82 arnivores, perissodactyls, artiodactyls, and cetaceans (e.g., 100% bootstrap value with both maximum

83 imple, two-dimensional ray-dynamics model of cetacean echolocation to examine the role played by coas

84 Modern phenomena driving cetacean ecology, such as trophic dynamics and arms race

85 However, cetacean embryos do initiate hind-limb bud development.

86 pment and physiology; however, their role in cetacean evolution is not clearly understood.

87 l competence, developed quickly and early in cetacean evolution, as soon as the taxa are associated w

88 ed a key 'point of no return' event in early cetacean evolution, leading to full independence from li

89 Early cetaceans evolved from terrestrial quadrupeds to obligat

90 ary of volatile and nonvolatile compounds in cetacean exhaled breath.

91 We found a D203G substitution in cetacean FGF9, which was predicted to affect FGF9 homodi

92 es the existence of a fossil lineage linking cetaceans (first known in the early Eocene) to hippos (f

93 It has never been attempted in cetaceans for comprehensive metabolite profiling.

94 eting our results in the context of both the cetacean fossil record and the known functions of Shh su

95 ined African elephant and several species of cetaceans (from smaller to larger brained) in comparison

96 The cetaceans had an average GI of 5.43, are the most gyrenc

97 ossil skeletons, the link to the ancestor of cetaceans has been missing.

98 g naivety has made this cryptic, deep-diving cetacean highly susceptible to disturbance, although qua

99 Our data indicate that the cetacean hind-limb bud forms an AER and that this struct

100 cological transitions dominate each phase of cetacean history, this context is rarely stated explicit

101 Compared to other cetaceans, humpback whales (Megaptera novaeangliae) have

102 rant investigation into the integrity of the cetacean immune system.

103 This methodology may hold promise for large cetaceans in the wild for which routine collection of bl

104 The number of VENs in these cetaceans is also comparable to data available from grea

105 he impact of noise over-exposure in stranded cetaceans is challenging, as the lesions that lead to he

106 The evolution of cetaceans is one of the best examples of macroevolution

107 ius), one of the closest extant relatives to cetaceans, is a large African even-toed ungulate (Artiod

108 Similar to contemporary primitive cetaceans, it probably swam by spinal extension with sim

109 Unlike other mammal species, cetaceans lack the enzyme for transforming an important

110 Eocene fossils document much of cetaceans' land-to-water transition, but, until now, the

111 recent discovery of rod monochromacy in some cetacean lineages provides a novel opportunity to invest

112 he MC4R from representative species of major cetacean lineages uniquely associated with the toothed w

113 ed bone density, is greatly increased in the cetacean liver under hypoxic conditions, thus implicatin

114 Here we assess the evolution of cetacean locomotor behaviour from an independent perspec

115 digestive and immune system functioning, yet cetacean microbiomes remain largely unexplored, in part

116 ntity plays an important role in structuring cetacean microbiomes, even at fine-scale taxonomic level

117 Cetacean morbillivirus (CeMV) is considered one of the m

118 ry transition that occurred independently in cetaceans, mosasauroids, chelonioids (sea turtles), icht

119 us associations between naval activities and cetacean MSEs, and an absence of other identifiable fact

120 of other identifiable factors known to cause cetacean MSEs, indicates naval activity to be the most p

121 sity data set, we show that much of observed cetacean paleodiversity can indeed be explained by diato

122 is increasing concern for the well-being of cetacean populations around the UK.

123 te change and marine exploitation on current cetacean populations may benefit from insights into what

124 Limited sequence data indicates that cetacean poxviruses (CPVs) belong to an unassigned genus

125 The fossil record of cetaceans provides an historical basis for understanding

126 ception of their vocalizations by unintended cetacean receivers may be particularly important in medi

127 ception of their vocalizations by unintended cetacean receivers may trigger anti-predator behavior th

128 These insights strengthen the case that cetaceans represent a peak in the evolution of nonhuman

129 nsitivity differences emerged when comparing cetaceans, seals and PB.

130 The odontocete cetaceans show an unusual form of mammalian sleep, with

131 cetaceans as seen in other mammals, with all cetaceans showing similar GIs irrespective of brain mass

132 ing any particular artiodactyl family as the cetacean sister group and supports monophyly of artiodac

133 While odontocete cetaceans sleep in an unusual manner, with unihemispheri

134 es indicate that VEN volume follows in these cetacean species a pattern similar to that in hominids,

135 nteractions between individuals of different cetacean species are often observed in the wild.

136 A survey of multiple cetacean species by PCR for gag, pol, and env sequences

137 Here we show that several cetacean species have very high mean blubber PCB concent

138 Here we examine a broader group of cetacean species in efforts to investigate how progester

139 s can mediate interactions between different cetacean species in previously unrecognized ways.

140 limate change on the geographic range of ten cetacean species in the eastern North Atlantic and to as

141 show that the distribution of VENs in these cetacean species is comparable to that reported in human

142 Several cetacean species show habitat-specific distributions of

143 With the technique now validated for these cetacean species, blubber P4 is a reliable diagnostic of

144 hod to reproducibly sample breath from small cetaceans, specifically Atlantic bottlenose dolphins (Tu

145 Using available cetacean stranding data bases from four disparate areas,

146 Cetacean strandings display a marked geographical cluste

147 that a number of coastlines known to attract cetacean strandings produce acoustical "Dead Zones" wher

148 are found in species representative of both cetacean suborders in addition to hominids and elephants

149 ence in the Prestin gene among some bats and cetaceans suggest that parallel adaptations for high-fre

150 ic amniote groups (sea snakes, sirenians and cetaceans), suggesting that this mode of sex determinati

151 integrated 23 years of aerial and shipboard cetacean surveys, linked them to environmental covariate

152 ction of this gene is no longer necessary in cetaceans that have lost most of their body hair.

153 population structure of a cryptic deep ocean cetacean, the Gray's beaked whale (Mesoplodon grayi).

154 rol and regulation of sleep in an odontocete cetacean, the harbor porpoise (Phocoena phocoena).

155 ting Odontoceti, and size, with the smallest cetacean, the vaquita, at 1.4 meters and the largest, th

156 specialists [4], we find evidence that stem cetaceans, the archaeocetes, were more sensitive to high

157 the skeletons of two early Eocene pakicetid cetaceans, the fox-sized Ichthyolestes pinfoldi, and the

158 documenting the presence of retroviruses in cetaceans, though the occurrences of cancers and immunod

159 of stranded (n = 929) or biopsied (n = 152) cetaceans, three out of four species:- striped dolphins

160 Dedicated agile swimming of cetaceans thus appeared to have originated as a rapid an

161 Morphological cladistic analyses have shown cetaceans to be most closely related to one or more meso

162 This is yet another parameter indicating cetaceans to be neuroanatomical outliers.

163 keletons also elucidate the relationships of cetaceans to other mammals.

164 ve been rendered nonfunctional in Odontoceti cetaceans (toothed whales, including dolphins and orcas)

165 webs continues to cause severe impacts among cetacean top predators in European seas.

166 ntral paradigm of aquatic locomotion is that cetaceans use fluke strokes to power their swimming whil

167 method to study reproduction in free-ranging cetaceans using biopsies.

168 Cetaceans utilize low bone density as a buoyancy control

169 volved in observing and recording individual cetaceans, very little is known about how they use their

170 , He=0.624-0.675), and, in contrast to other cetaceans, we found a complete lack of genetic structure

171 The infected captive cetaceans were either subclinical, or clinical signs inc

172 undetermined encephalitides in free-ranging cetaceans were studied retrospectively.

173 rders Perissodactyla + Cetartiodactyla minus cetaceans) were merged with host trait data and IUCN Red

174 nd control found in other mammals, including cetaceans, were present in the river hippopotamus, with

175 e cognitive capacities of dolphins and other cetaceans (whales and porpoises) has importance for the

176 Among mammals, modern cetaceans (whales, dolphins, and porpoises) are unusual

177 lutionary lineage from microchiropterans and cetaceans (which have evolved ultrasonic hearing to mini

178 pelvic paddling, unlike later sirenians and cetaceans, which lost the hindlimbs and enlarged the tai

179 The fully aquatic cetaceans would similarly benefit from cognitive cardiov