ライフサイエンスコーパス: bottlenose dolphin

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

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

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

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

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

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

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

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

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

10 Bottlenose dolphins develop their own unique identity si

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

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

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

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

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

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

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

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

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

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

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

22 In bottlenose dolphins, remarkable small-scale differences

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

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

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

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

27 Bottlenose dolphins therefore appear to be unique as non

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

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

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

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

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

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

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

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

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

37 Bottlenose dolphins (Tursiops truncatus) are a promising

38 Bottlenose dolphins (Tursiops truncatus) develop individ

39 Echolocating bottlenose dolphins (Tursiops truncatus) discriminate be

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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