ライフサイエンスコーパス: carnivorous

1 s, prompted the suggestion that the genus is carnivorous.

2 ibalism among insects that typically are not carnivorous.

3 did barnacle (>1,500 individuals m(-2)), and carnivorous actinostolid anemone (>30 individuals m(-2))

4 and confirms the close relationship between carnivorous action and plant defense mechanisms.

5 nterpreted as the diversification of various carnivorous and cursorial taxa, whereas the acquisition

6 systems [5], due to community respiration of carnivorous and detritivorous zooplankton.

7 w to be one of the most enormous terrestrial carnivorous animals ever.

8 re a separate phylum (Chaetognatha) of small carnivorous animals, dominantly pelagic, and a major com

9 hemical mimicry of the food sources of adult carnivorous animals.

10 e) in H. monstrosus may have facilitated the carnivorous aspect of its diet.

11 herbivorous arthropods, and indirectly serve carnivorous (beneficial) arthropods by providing food an

12 ranging apex felid predators with a strictly carnivorous diet, could also be effective secondary long

13 d natural endocranial cast (endocast) from a carnivorous dinosaur of the late Jurassic period, Allosa

14 s did, in fact, evolve from certain types of carnivorous dinosaur.

15 nt to our knowledge of the feeding habits of carnivorous dinosaurs and for accurate reconstruction th

16 s, but until now the evidence in relation to carnivorous dinosaurs has been sparse and anecdotal.

17 Prey-capture strategies in carnivorous dinosaurs have been inferred from the biomec

18 Tyrannosaurids--the familiar group of carnivorous dinosaurs including Tyrannosaurus and Albert

19 tionary history of Maniraptora, the clade of carnivorous dinosaurs that includes birds and the sickle

20 rannosauridae, the best known group of large carnivorous dinosaurs, and determine the developmental m

21 final two stages of the Cretaceous, whereas carnivorous dinosaurs, mid-sized herbivores, and some As

22 test gait and speed of the largest theropod (carnivorous) dinosaurs, such as Tyrannosaurus, is contro

23 also regulates volatile signals that attract carnivorous enemies of herbivores or warn neighboring pl

24 Our results demonstrate that strictly carnivorous, felid predators could have broad and overlo

25 CE across 3 trophic levels (phytoplankton to carnivorous fish) was highest under low light and high n

26 s evolved independently from a plesiomorphic carnivorous form.

27 ic analyses support ctenophores, a phylum of carnivorous, gelatinous marine organisms, as the sister

28 ous mammals have a relatively high slope and carnivorous, insectivorous, and nectarivorous birds have

29 s in scaling exponents among herbivorous and carnivorous mammals and birds.

30 to their mother of origin and concluded that carnivorous mammals can be better dispersers than birds.

31 Most carnivorous mammals can pulverize skeletal elements by g

32 50 million years, successive clades of large carnivorous mammals diversified and then declined to ext

33 FMRs and desert birds have low FMRs; and (g) carnivorous mammals have a relatively high slope and car

34 fornianus) are members of a diverse clade of carnivorous mammals known as pinnipeds.

35 mirrored differences between herbivorous and carnivorous mammals, reflecting trade-offs between carbo

36 ng other reptiles, fish, and herbivorous and carnivorous mammals.

37 phan in peptides recovered from the venom of carnivorous marine cone snails (Conus).

38 of the Plantaginaceae, a family in which no carnivorous members are otherwise known.

39 that controls prey capture reactions in the carnivorous mollusc Clione limacina.

40 f-contained pools that form in leaves of the carnivorous northern pitcher plant, Sarracenia purpurea.

41 pulations, where L. humile is among the most carnivorous of ants, Argentine ants from California occu

42 esentative genomes from across Mammalia with carnivorous, omnivorous, and herbivorous dietary special

43 However, the production of carnivorous organs can be a phenotypically plastic trait

44 tic costs associated with the maintenance of carnivorous organs.

45 nsect communities, that harvesting of single carnivorous parasitoid species led to a significant incr

46 repeatable, passive-dynamic motion used by a carnivorous pitcher plant to catch prey.

47 Carnivorous pitcher plants capture prey with modified le

48 nteresting group of proteolytic enzymes from carnivorous pitcher plants of the genus Nepenthes.

49 In order to evaluate interactions between a carnivorous plant (greater bladderwort, Utricularia vulg

50 imentally demonstrate interactions between a carnivorous plant and a fish.

51 teine protease from the digestive fluid of a carnivorous plant and confirms the close relationship be

52 A new study shows that a carnivorous plant attracts bats by possessing modified p

53 the uptake of N via roots versus prey of the carnivorous plant Drosera rotundifolia growing in ombrot

54 logical features with extant Roridulaceae, a carnivorous plant family that is today endemic to the Ca

55 significant investment of the resources of a carnivorous plant is committed to producing the traps, a

56 ple of convergent evolution across unrelated carnivorous plant lineages.

57 No case of carnivorous plant traps has so far been reported from th

58 ocument both a unique capturing strategy for carnivorous plants and a case of a plant that traps and

59 share a common prey could exist than between carnivorous plants and animals.

60 e considered inter-Kingdom competition among carnivorous plants and animals.

61 Modern Roridula species are unique among carnivorous plants as they digest prey in a complex mutu

62 pitcher secretions of the Nepenthes genus of carnivorous plants contain a proteolytic activity that i

63 ase (COX) from an active-trapping lineage of carnivorous plants is caused by positive Darwinian selec

64 The fossil record of carnivorous plants is very scarce and macrofossil eviden

65 Our data suggest that carnivorous plants may actively promote or reduce animal

66 Carnivorous plants primarily use aspartic proteases duri

67 t similarities of Philcoxia to those of some carnivorous plants, along with recent observations of ne

68 ical, and physiological) and mutualisms with carnivorous plants, and the ecological and agricultural

69 sensitive to increasing nutrient input, and carnivorous plants, which are characteristic of these wi

70 en active and passive trapping mechanisms in carnivorous plants.

71 insufficient to explain the movement of all carnivorous polar bears.

72 from RLB was more omnivorous than the highly carnivorous populations from the Northwest.

73 Prey shifts in carnivorous predators are events that can initiate the a

74 ction in repelling herbivores and attracting carnivorous predators in green tissues, the presumed pri

75 Conversely, carnivorous reptiles have non-occluding dentitions that

76 Oxygen consumption by carnivorous reptiles increases enormously after they hav

77 homys leucogaster) are among the most highly carnivorous rodents in North America.

78 rements in the pelagic prey-predator system (carnivorous sculpins and top-predator seals).

79 on of an alien biological control agent: the carnivorous snail Euglandina rosea[3].

80 he late Pleistocene, during which many large carnivorous species coexisted as predators and competito

81 effect is of particular interest because two carnivorous species of sea turtles-hawksbills, Eretmoche

82 Farming carnivorous species requires large inputs of wild fish f

83 anism, and they demonstrate the ability of a carnivorous species to respond to the availability of re

84 e origin, distribution, and frequency of the carnivorous syndrome in angiosperms and, more generally,

85 trophic webs with a seeming overabundance of carnivorous taxa and the evolution of entirely new preda

86 rnivores in a community and low diversity of carnivorous taxa, whereas higher oxygen levels support m

87 g a stream productivity gradient, as well as carnivorous terrestrial invertebrates, in a forested wat

88 his technique to the long skull of the large carnivorous theropod dinosaur Allosaurus fragilis.

89 saurs nested within a clade of predominantly carnivorous theropods, are known to have had teeth, wher

90 Feeding, for example, ranges from carnivorous, through subaquatic and terrestrial omnivoro

91 ated with the grass carp's adaptation from a carnivorous to an herbivorous diet.

92 t evidence for the presence of a terrestrial carnivorous vertebrate from the Middle Permian of South

93 light may enable predation of zooplankton by carnivorous zooplankters, fish, and birds now known to f