ライフサイエンスコーパス: bottlenose dolphin

1 stems in the most well-studied cetacean, the bottlenose dolphin.

2 mporary pairs of coastal-pelagic ecotypes of bottlenose dolphin.

3 iven by habitat specialization in the common bottlenose dolphin.

4 onvergent evolution of motherese, or CDC, in bottlenose dolphins.

5 bacterial structures (RBSs) in the mouths of bottlenose dolphins.

6 here report the surprising finding that the bottlenose dolphin, a toothed whale, is clustered with m

7 We used stable isotope data from common bottlenose dolphins across the Gulf of Mexico to determi

8 uences of three minke whales, a fin whale, a bottlenose dolphin and a finless porpoise.

9 clear-to-cytoplasmic ratio of 4 Indo-Pacific bottlenose dolphins and 2 human thyroid glands.

10 Analysis of over 850 samples from 105 bottlenose dolphins and associated prey items were analy

11 mals and exploration of these differences in bottlenose dolphins and other marine mammals may identif

12 demonstrates the highly plastic behaviour of bottlenose dolphins and shows a previously unreported be

13 tis virus has been detected in wild Atlantic bottlenose dolphins, and captive orcas have been killed

14 h unique vocal behavior, including macaques, bottlenose dolphins, and Egyptian fruit bats, and we eva

15 Bottlenose dolphins are highly social, renowned for thei

16 Because bottlenose dolphins are long-lived mammals that develop

17 Because bottlenose dolphins are long-lived mammals that exhibit

18 HPRT1 and RPL4 were the most stable HKGs in bottlenose dolphin blood.

19 ut of four species:- striped dolphins (SDs), bottlenose dolphins (BNDs) and killer whales (KWs) had m

20 signals among conspecifics, because captive bottlenose dolphins can be trained to use novel, learned

21 ist in the circulating blood proteome of the bottlenose dolphin compared to terrestrial mammals and e

22 ern Australia, groups of 4-14 unrelated male bottlenose dolphins cooperate in second-order alliances

23 Bottlenose dolphins develop their own unique identity si

24 In July 2023, three bottlenose dolphins developed neurological symptoms and

25 In 2004, 105 bottlenose dolphins died in the absence of an identifiab

26 In 2005/2006, 90 bottlenose dolphins died that were initially coincident

27 This study demonstrates that bottlenose dolphins extract identity information from si

28 n multistate model to investigate changes in bottlenose dolphin fecundity and calf survival.

29 In Shark Bay, Western Australia, male bottlenose dolphins form a complex nested alliance hiera

30 Shark Bay, Western Australia, unrelated male bottlenose dolphins form multilevel alliances, where mal

31 Male bottlenose dolphins form persisting multi-level alliance

32 ng/g (wet weight [wet wt]) in the livers of bottlenose dolphins from Sarasota Bay, FL.

33 Analysis of the bottlenose dolphin genome revealed two full-length provi

34 Our results show that most bottlenose dolphin geographical units find their habitat

35 atric pelagic and coastal ecotypes of common bottlenose dolphins have repeatedly formed across the oc

36 oncern for marine wildlife, including common bottlenose dolphins in sensitive coastal habitats.

37 However, a population of bottlenose dolphins in Shark Bay, Western Australia, com

38 uring brief catch-and-release events of wild bottlenose dolphins in waters near Sarasota Bay, Florida

39 lysed the distribution and movements of 4919 bottlenose dolphins, individually identified through the

40 The common bottlenose dolphin is a cosmopolitan species that can be

41 In the Mediterranean Sea, the common bottlenose dolphin is a regularly occurring species and

42 According to some studies, the Mediterranean bottlenose dolphin is more closely related to the Atlant

43 Together, these results suggest that bottlenose dolphin leaders have the opportunity to gain

44 in was the causative agent involved in these bottlenose dolphin mortality events.

45 unlike terrestrial mammals, killer-whale and bottlenose-dolphin neonates and their mothers show littl

46 Therefore, we tested 8 bottlenose dolphins on an object retrieval task.

47 effect of noise on coordination between two bottlenose dolphins performing a cooperative task.

48 ) model to predict PCB concentrations in the bottlenose dolphin population of Charleston, SC, USA, wa

49 e, we analyze the acoustic emissions of nine bottlenose dolphin populations across the Atlantic Ocean

50 uishes the eastern and western Mediterranean bottlenose dolphin populations has no strong influence o

51 Results demonstrate that the bottlenose dolphin possesses prominent perivascular spac

52 The IB model for PCBs in bottlenose dolphins provides a novel approach to estimat

53 In bottlenose dolphins, remarkable small-scale differences

54 Here, we show that wild bottlenose dolphins respond to hearing a copy of their o

55 tecting H. cetorum were compared for 20 wild bottlenose dolphins sampled as part of a long-term healt

56 oadband results suggest that an echolocating bottlenose dolphin should be able to detect a 7.62-cm di

57 we discuss some of the defining features of bottlenose dolphin social and vocal complexity and place

58 vocal learning and cultural transmission in bottlenose dolphin societies.

59 Here we investigate whether Shark Bay bottlenose dolphins that use marine sponges as hunting t

60 Bottlenose dolphins therefore appear to be unique as non

61 that estimated ages in several species from bottlenose dolphins to bowhead and humpback whales using

62 hological features of the clitoris in common bottlenose dolphins to examine functional features, incl

63 c monitoring to characterize the response of bottlenose dolphins to intense storms offshore Maryland,

64 ation of six eNA components derived from the bottlenose dolphin Tursiops truncatus: mitochondrial eDN

65 physiological impacts of HOC exposure in two bottlenose dolphin ( Tursiops truncatus) ecotypes in the

66 sm of foraging behaviors in the Indo-Pacific bottlenose dolphin (Tursiops aduncus) population of Shar

67 dance and temporary emigration of a resident bottlenose dolphin (Tursiops aduncus) population off Bun

68 ic data on Shark Bay's resident Indo-Pacific bottlenose dolphin (Tursiops aduncus) population reveale

69 g experiments were conducted with a resident bottlenose dolphin (Tursiops aduncus).

70 of both rod and cone visual pigments of the bottlenose dolphin (Tursiops truncatus) are blue-shifted

71 ix distinct geographical units of the common bottlenose dolphin (Tursiops truncatus) in the Mediterra

72 The hearing sensitivity of an Atlantic bottlenose dolphin (Tursiops truncatus) to both pure ton

73 er tarandus), griffon vulture (Gyps fulvus), bottlenose dolphin (Tursiops truncatus), American flamin

74 For the common bottlenose dolphin (Tursiops truncatus), studies on acou

75 cortices of small odontocetes, including the bottlenose dolphin (Tursiops truncatus), the Risso's dol

76 is capable of vocal production learning, the bottlenose dolphin (Tursiops truncatus).

77 us neoformans var. gattii in a male Atlantic bottlenose dolphin (Tursiops truncatus).

78 humpback (Sousa sahulensis) and Indo-Pacific bottlenose dolphins (Tursiops aduncus) around the North

79 In Western Australia, adult male bottlenose dolphins (Tursiops aduncus) form multilevel a

80 two well-studied populations of Indo-Pacific bottlenose dolphins (Tursiops aduncus) in south-western

81 handouts to a limited number of free-ranging bottlenose dolphins (Tursiops aduncus).

82 In Shark Bay, Western Australia, male bottlenose dolphins (Tursiops sp.) cooperate in pairs an

83 background and socio-cognitive skill-set of bottlenose dolphins (Tursiops sp.), alongside the specia

84 Populations of bottlenose dolphins (Tursiops spp.) vary in male allianc

85 son of undepleted serum proteins from common bottlenose dolphins (Tursiops truncatus) and pooled norm

86 rams, behaviour and flipper accelerations of bottlenose dolphins (Tursiops truncatus) and Weddell sea

87 Bottlenose dolphins (Tursiops truncatus) are a promising

88 Bottlenose dolphins (Tursiops truncatus) are keystone an

89 Bottlenose dolphins (Tursiops truncatus) develop individ

90 Echolocating bottlenose dolphins (Tursiops truncatus) discriminate be

91 riate reference genes in blood leukocytes of bottlenose dolphins (Tursiops truncatus) for gene transc

92 olonies in the Great Lakes in 2010-2012, and bottlenose dolphins (Tursiops truncatus) from Sarasota B

93 In the Florida Panhandle region, bottlenose dolphins (Tursiops truncatus) have been highl

94 xGC-TOF/MS analysis of blubber from 8 common bottlenose dolphins (Tursiops truncatus) inhabiting the

95 luoroalkyl substances (PFAS) in free-ranging bottlenose dolphins (Tursiops truncatus) inhabiting two

96 form assessments of the impact of bycatch on bottlenose dolphins (Tursiops truncatus) interacting wit

97 ified in blubber from two ecotypes of common bottlenose dolphins (Tursiops truncatus) sampled in the

98 the southwestern Atlantic Ocean, tissue from bottlenose dolphins (Tursiops truncatus) stranded or inc

99 udied cross-modal, individual recognition in bottlenose dolphins (Tursiops truncatus) that use signat

100 rship has been documented in a population of bottlenose dolphins (Tursiops truncatus) where direct be

101 , tidal and diel cycles on the occurrence of bottlenose dolphins (Tursiops truncatus) within a Marine

102 tocetes (e.g., killer whales (Orcinus orca), bottlenose dolphins (Tursiops truncatus), and white-beak

103 evidence for episodic-like memory in common bottlenose dolphins (Tursiops truncatus), based on the i

104 female-female sexual interactions in common bottlenose dolphins (Tursiops truncatus), which rub each

105 microbes in the oral gingival sulcus of two bottlenose dolphins (Tursiops truncatus).

106 from small cetaceans, specifically Atlantic bottlenose dolphins (Tursiops truncatus).

107 and manipulation in 4 juvenile male captive bottlenose dolphins (Tursiops truncatus).

108 , and during recovery from apnea in 11 adult bottlenose dolphins (Tursiops truncatus, 9 males and 2 f

109 phatic and glymphatic structures in stranded bottlenose dolphins (Tursiops truncatus; n = 9) using im

110 The authors tested 2 bottlenosed dolphins (Tursiops truncatus) for their unde

111 in [Lagenorhynchus obliquidens]; an Atlantic bottlenose dolphin [Tursiops truncatus]; and a beluga wh

112 s and maintenance of individual variation in bottlenose dolphins' Tursiops aduncus niche.

113 ies and determined the habitat use of common bottlenose dolphins, Tursiops truncatus truncatus, from

114 els were compared among 55 individual common bottlenose dolphins, Tursiops truncatus, in Sarasota Bay

115 Between 1999 and 2006, three bottlenose dolphin UMEs occurred in the Florida Panhandl

116 This report shows that wild, unrestrained bottlenose dolphins use their learned whistles in matchi

117 t support for convergence among bats and the bottlenose dolphin was seen in numerous genes linked to

118 concentrations predicted in male and female bottlenose dolphin were in good agreement with observed

119 Indo-Pacific bottlenose dolphins were sighted more often than Austral

120 Seventy-five blood samples collected from 7 bottlenose dolphins were used to analyze 15 candidate HK

121 istles and 860 test whistles from common and bottlenose dolphins were used) demonstrate that SAM-whis

122 ction is not restricted to the sea lion: the bottlenose dolphin, which evolved independently from the

123 studies have investigated the variability of bottlenose dolphin whistles between populations, very fe

124 st this hypothesis in wild male Indo-Pacific bottlenose dolphins, who form multi-level alliances that

125 ions were performed on 15 apparently healthy bottlenose dolphins with both PUS and FCUS under identic

126 and more nearshore waters than Indo-Pacific bottlenose dolphins, yet these species co-occurred more