ライフサイエンスコーパス: twig

1 ted neurons were distributed across multiple twigs.

2 octed using either cacao or holly leaves and twigs.

3 etween wood tissues from trunk, branches and twigs.

4 an avian predator by being misidentified as twigs.

5 sting ants than a monospecific collection of twigs.

6 is 47 +/- 5, significantly fewer than in the twigs (90 +/- 7), which in turn is significantly fewer v

7 Omission of individual twigs accounted for 96% of errors.

8 Leaf and twig anatomical traits were better predictors of all dem

9 obustness of a strong connection to detailed twig anatomy was associated with robustness to reconstru

10 otential, photosynthetic rates/capacity, and twig and needle growth.

11 patterns responded to an interaction between twigs and agriculture, consistent with a functional resp

12 evelopment, and food availability from woody twigs and agriculture.

13 these pathogens can move between fruits and twigs and display latent pathogen lifestyles.

14 reatly in mechanical properties: flexible in twigs and in the stem of the sapling, and rigid in the o

15 ortriterpenoids (1-8) were isolated from the twigs and leaves of the Chinese mangrove plant Xylocarpu

16 of living trees and other surfaces, such as twigs and soils, using a static closed-chamber method, a

17 Tools consisted of twigs and sticks, often modified, which were used to pro

18 dii of xylem conduits from trunk to terminal twig, and how the frequency of xylem conduits varies wit

19 arious levels of complexity (such as leaves, twigs, and branches).

20 oassay-directed fractionation of the leaves, twigs, and flowers of Miliusa sinensis Finet and Gagnep.

21 tent across years, we re-sampled P. flexilis twigs at Niwot Ridge, CO and characterized needle endoph

22 experimentally show that a diverse array of twigs attracted 80% more species of twig-nesting ants th

23 larger, more resolved, and better-evaluated TWiG-based hypothesis supports the grouping of dromaeosa

24 ical levels and patterns of NSC variation in twigs, branches and trunks whereas pistachio and walnut

25 leaf CO production and flux using automated twig chambers on mature Pinus halepensis trees grown und

26 ated analysis of the Theropod Working Group (TWiG) coelurosaurian phylogenetic data matrix.

27 novel sounds to awareness, such as that of a twig cracking under the paw of a stalking predator in a

28 appears that diversity per se at one level (twigs) creates conditions that promote diversity at anot

29 ricultural land was plentiful, greater woody twig density was associated with more pronounced activit

30 agricultural land was limited, greater woody twig density was associated with reduced activity during

31 MG was found broadly throughout the twig except in the xylem.

32 pounds; both were distributed throughout the twig except the xylem.

33 for nitrogenase activity within P. flexilis twigs four times from June to September.

34 of insects and fungi collected from dormant twigs from 155 tree species at 51 botanical gardens or a

35 endophytic fungal communities of olive tree twigs from three different cultivars, was investigated i

36 ration differences among plant parts whereby twigs had the highest and most variable NSC concentratio

37 for this, however, is limited to saplings or twigs in climate-controlled chambers.

38 and sugar levels in both xylem and phloem of twigs in Prunus dulcis, Pistacia vera and Juglans regia.

39 plate by a penetrating foreign body (wooden twig) in an adult male who presented with discharging si

40 ty of masqueraders relative to their models (twigs, in our system) increases.

41 We conclude that HDX of protein ions in a TWIG is highly sensitive to protein conformation, enable

42 ecies and tissues (i.e., roots, trunk/cores, twigs, leaves/needles) of the local plant community were

43 nger to attack larvae that were resting in a twig-like posture than larvae resting flat against a bra

44 energetically stress larvae) adopted a less twig-like posture than larvae that were fed ad libitum.

45 ntroduced into either the source TWIG or the TWIG located just after the ion mobility cell, such that

46 oratory experiments with avian predators and twig-mimicking caterpillars as masqueraders to investiga

47 Here we report a series of experiments with twig-mimicking larvae of the American peppered moth Bist

48 array of twigs attracted 80% more species of twig-nesting ants than a monospecific collection of twig

49 strol (2), were isolated from the fruits and twigs of Aglaia silvestris by bioassay-guided fractionat

50 omic data matrices to infer the branches and twigs of the tree of life.

51 demonstrate that a traveling wave ion guide (TWIG) of a Synapt mass spectrometer offers a highly suit

52 extracts (70%) from aerial parts (leaves and twigs) of S. paniculatum led to the isolation of the two

53 ND(3) was introduced into either the source TWIG or the TWIG located just after the ion mobility cel

54 ly anchored rather than attached to flexible twigs or stems.

55 ng objects in the local environment (such as twigs or stones), demonstration of antipredatory benefit

56 st, with the largest differences observed in twigs originating from regions with higher mean annual t

57 d starch) in the leaf lamina, main veins and twigs over 24 h.

58 he path fraction, Pf : mean/maximum trunk-to-twig pathlength.

59 oning and allocation towards leaf starch and twig phloem sugars was influenced by the plant water sta

60 genome size enlarged bark and wood layers in twigs sampled in the field.

61 in such phrases as "a flash of light" or "a twig snap".

62 exopyranoside extracted from Nerium oleander twigs that displays anti-inflammatory properties and cel

63 Direct analysis of kratom twig tissue revealed distinct spatial distributions for

64 faster, but as the lizards shifted onto high twigs to avoid the predator, selection would reverse tow

65 We collected 18 leaf and twig traits from 29 tree species in a tropical freshwate

66 the initiation of flowering, Psi(PD) of the twig was - 0.72 MPa and gradually rose to - 0.17 MPa by

67 ange (DeltaPsi) in twig water potential (Psi(twig)) was in the post-monsoon season.

68 The highest seasonal change (DeltaPsi) in twig water potential (Psi(twig)) was in the post-monsoon

69 Likewise, the twig water potential corresponding to the threshold for

70 twig water potentials (Psi(PD)) and mid-day twig water potentials (Psi(MD)) were - 0.81 and - 1.24 M

71 sites, and years, the most negative pre-dawn twig water potentials (Psi(PD)) and mid-day twig water p

72 yield information and monthly NSC content in twigs, we show that high levels of carbohydrate in Prunu

73 The specific tree species from which the twigs were derived did not explain the pattern.

74 Beetles (bark/twig) were present in 92% of dead trees.

75 located on numerous small, microtubule-free 'twigs' which branch off a single microtubule-containing

76 ytes have access to foliar N2 , we incubated twigs with (13) N2 -enriched air and imaged radioisotope

77 ibitory effects of water extract from longan twigs (WLTs) on mutation and nitric oxide (NO) productio

78 , we also observed changes in delta(18) O of twig xylem water.