ライフサイエンスコーパス: hatchling

1 torecipient structures resembled that of the hatchling.

2 before and after colonization of 1,500 squid hatchlings.

3 as has been hypothesized for precocial bird hatchlings.

4 ment and produce many small eggs and smaller hatchlings.

5 n of auditory preferences in precocial avian hatchlings.

6 eding field plots with rare and common giant hatchlings.

7 alis and E. faecium kill C. elegans eggs and hatchlings, although only E. faecalis kills the adults.

8 is the change from fully toothed jaws in the hatchling and juvenile individuals to a completely tooth

9 examined after unilateral cochlea removal in hatchlings and 3-week-old birds.

10 was restricted to the liver and intestine of hatchlings and adult zebrafish, whereas zRetSat B was ex

11 ing success of each clutch, and assessed all hatchlings and dead embryos for gross morphological malf

12 caretta), which leave their home beaches as hatchlings and migrate across entire ocean basins before

13 presence of three components in UV cones of hatchlings and terrestrial adults ruled out a developmen

14 expression and polysiaylation in embryonic, hatchling, and adult chick corneas.

15 Caenorhabditis elegans hatchlings arrest in a dormant state termed "L1 diapause

16 ells become necrotic and kill E. solidaginis hatchlings before gall induction.

17 (NO) has been implicated in learning in the hatchling chicken.

18 studied in the vestibular nuclei of 4-5-day hatchling chicks by using single and double labeling of

19 Cochleae from hatchling chicks were placed in culture, and hair cells

20 erior rectus and superior oblique muscles of hatchling chicks were treated in vivo either to increase

21 ed in learning of passive avoidance tasks in hatchling chicks.

22 erve and NM on both sides were obtained from hatchling chicks.

23 n the telencephalon are similar in adult and hatchling Columbiformes.

24 sting was chronically blocked with curare in hatchlings, dark-induced expansion of receptive fields w

25 southern Japan is remarkably stable and that hatchling dispersal to oceanic habitats itself does not

26 e active season (November), an age cohort of hatchlings emerges; larger juveniles or adults are not p

27 Estrogen treatment of hatchling females caused an increase in the expression o

28 sked how head skin stimuli evoke swimming in hatchling frog tadpoles.

29 These hatchlings grow rapidly, reach sexual maturity in less t

30 Hatchlings had bufadienolides in their nuchal glands onl

31 d survival to be strongly age dependent with hatchlings having the lowest survival rates (16%) but in

32 g incubation temperatures on the survival of hatchlings in nests.

33 In hatchlings, Kv1.2 staining decreased in the cell bodies

34 ocations of the amphidial cell bodies in the hatchling larva (L1) were compared with their locations

35 lation of specifically recognized neurons in hatchling larvae (L1) in which neuronal cell bodies are

36 e finger cell neurons (AFD), were ablated in hatchling larvae with a laser microbeam, and these were

37 give rise to a horizontal stripe pattern in hatchling larvae.

38 Here we report, however, that hatchling loggerhead sea turtles (Caretta caretta) from

39 Here we report that hatchling loggerheads, when exposed to magnetic fields r

40 HVC and area X by P11, whereas treatment of hatchling males with the aromatase inhibitor fadrozole d

41 Hatchling mass was not affected.

42 termination to a focus on temperature-linked hatchling mortalities.

43 show the generality of relationships between hatchling mortality and incubation temperature and hence

44 uggests that the remains represent precocial hatchlings of enantiornithine birds.

45 officinalis and were compared with those in hatchlings of two other cephalopod species.

46 ees C, temperatures that produce only female hatchlings or a male-biased sex ratio, respectively.

47 High levels of mortality among nests, hatchlings or maturing turtles produced in the Melbourne

48 he linked effects of warming temperatures on hatchling output and on sex ratios for these species tha

49 Hatchling output increased with long-term precipitation

50 e effect of local climatic conditions on the hatchling output of leatherback turtles (Dermochelys cor

51 High air temperature reduced hatchling output only at the area experiencing seasonal

52 On predator-introduction islands, those hatchling populations were a smaller fraction of pre-hur

53 found that although, ordinarily, cuttlefish hatchlings prefer shrimp-like prey, when visually expose

54 kely to provide conditions suitable for male hatchling production in a warming world.

55 oraging females that provide higher rates of hatchling production.

56 also performed feeding experiments in which hatchling R. tigrinus were reared on controlled diets th

57 ields of ganglion cells exposed to curare in hatchlings reared in normal light and dark cycles were s

58 ced hatchling sex ratios of 53% and 63% male hatchlings, respectively, for hawksbill and green turtle

59 ipheral and central trigeminal structures in hatchling ring doves.

60 s which would likely produce fairly balanced hatchling sex ratios of 53% and 63% male hatchlings, res

61 eratures at nest depths and implications for hatchling sex ratios of hawksbill turtles (Eretmochelys

62 t microtubule-associated protein 2 (MAP2) in hatchlings showed that some Kv1.1 remained as clusters w

63 hal warming decreased embryonic survival and hatchling sizes.

64 oduction and fertility resulted in decreased hatchling success (p = 0.023).

65 anagement practices are focused on nests and hatchling survival; however, protection efforts that ext

66 and three (13%) produced germline transgenic hatchlings that expressed the GFP protein (F1).

67 Finally, in the hatchling, the vast majority of principal cells is capab

68 Precocial avian hatchlings thus likely play a more active role in direct

69 a biological means used by extant sea turtle hatchlings to elevate metabolic and growth rates - had e

70 oss-fostered eggs and tested the response of hatchlings to the scent of genetic vs. foster parents.

71 Over the study period, 7,427 hatchlings were marked and 380 individuals were recaptur

72 natal dinosaurs suggests that known dinosaur hatchlings were precocial.

73 A minimum of 529 hatchlings were produced on Ile aux Aigrettes in 11 year

74 Naive hatchlings will feed and grow successfully on many diffe

75 By studying simple hatchling Xenopus laevis tadpoles, we have already ident

76 When the hatchling Xenopus tadpole swims, responses to cutaneous

77 erneurons that drive the swimming CPG in the hatchling Xenopus tadpole, may contribute to the mainten

78 swimming is initiated by tail stimulation in hatchling Xenopus tadpoles, the first trunk contraction

79 a subset of turtles (n = 513), we estimated hatchling yields associated with each hotspots.

80 he synthesis of DHT from testosterone (T) in hatchling zebra finches.