ライフサイエンスコーパス: woody plant

1 CO2 and fire shifted the balance in favor of woody plants.

2 demonstrated increasing representation of C3 woody plants.

3 emicals, and otherwise facilitate feeding on woody plants.

4 grasses, which scavenge the water lifted by woody plants.

5 ke, translocation, and transformation within woody plants.

6 f geometries, based on a survey of temperate woody plants.

7 ernal hydraulic and carbohydrate dynamics of woody plants.

8 ay be a defining characteristic of perennial woody plants.

9 ocots and eudicots or between herbaceous and woody plants.

10 d and cambium tissues, which are specific to woody plants.

11 echanisms of delayed competence to flower in woody plants.

12 describes the impact of large herbivores on woody plant abundance mediated by herbivore diversity an

13 ly, we tested field-based eCa experiments on woody plants across the globe for a relationship between

14 the early and late signal exchanges between woody plants and ECM fungi, and we suggest future direct

15 the appearance of moist tundra dominated by woody plants and graminoids.

16 The coexistence of woody plants and grasses in savannas is determined by a

17 mechanism responsible for the coexistence of woody plants and grasses in savannas.

18 und a prevalence of quantitative defenses in woody plants and qualitative defenses in herbaceous plan

19 ost widespread associations between roots of woody plants and soil fungi in forest ecosystems.

20 e evolution of abundant lignin production in woody plants and the subsequent evolution of lignin-degr

21 might allow for the coexistence of overstory woody plants and understory grasses.

22 rsors controls lignin monomer composition in woody plants, and that F5H over-expression is a viable m

23 lly the N-fixing ability and architecture of woody plants, are critical to predicting encroachment ov

24 rapid, drought-induced die-off of overstory woody plants at subcontinental scale and highlight the p

25 hips using a global compilation of ecosystem woody plant biomass and production data.

26 nown about the major polymeric components of woody plant biomass, with an emphasis on the molecular i

27 more cost-effective production of fuel from woody plant biomass.

28 lex events that lead to the formation of the woody plant body.

29 n of vascular systems of both herbaceous and woody plants, but relatively little is known about the p

30 Pit membranes have been well studied in woody plants, but very little is known about their funct

31 of the variation in ozone sensitivity among woody plants can be explained by interspecific variation

32 ndscapes characterized by intense herbivory, woody plants can persist by defending themselves or by a

33 acea can degrade all polymeric components of woody plant cell walls, a characteristic of white rot.

34 nd seed size) were estimated for four to six woody plant clades (Acer, Aesculus, Ceanothus, Arbutoide

35 rguing, based on an analysis of NPP for 1247 woody plant communities across global climate gradients,

36 Here, using data from woody plant communities from different biogeographic reg

37 This effect is large considering that woody-plant cover has been described as increasing at 0.

38 iched as both U(IV) and U(VI) on fibrous and woody plant debris (48 +/- 10% U(IV), x +/- sigma, n = 2

39 ant trend; however, the species diversity of woody plants decreased linearly towards the village boun

40 stable groundwater resource, and increasing woody plant density decoupled NEP and ET from incident p

41 erface between land and sea at the margin of woody plant distribution.

42 undergoing a rapid shift from herbaceous to woody-plant dominance.

43 sing nitrogen availability, productivity and woody-plant dominance.

44 ivestock production (LP), but the impacts of woody-plant encroachment on this crucial ecosystem servi

45 lower (by 1-2.7 per thousand) than for other woody plant functional types (PFT), likely due to greate

46 l distributions of the related, hyperdiverse woody plant genera Psychotria and Palicourea (Rubiaceae)

47 t species of the region, we found that large woody plants generally have greater PII values than othe

48 parasites, are the most common components of woody plant genomes.

49 has stabilized tropical forests by promoting woody plant growth, despite increased aridity.

50 ole in defense against pathogen infection in woody plants has not been investigated comprehensively.

51 m season forage grasses they are displacing, woody plants have a photosynthetic metabolism and carbon

52 cold acclimation in numerous herbaceous and woody plants, have been speculated to provide, among oth

53 manipulated leaf out of invasive and native woody plants in Concord, MA, USA.

54 t efficiency in seedless vascular plants and woody plants in equal measure by compensating for shorte

55 a common virus-induced disease of perennial woody plants induced by a range of different viruses.

56 esis has been advanced that the incursion of woody plants into world grasslands over the past two cen

57 Here we investigate woody plant invasion along a precipitation gradient (200

58 Assessments relying on carbon stored from woody plant invasions to balance emissions may therefore

59 ty, predicting that herbivore suppression of woody plants is strongest where herbivore diversity is h

60 The endophytic fungi of woody plants may be diverse as often claimed, and likewi

61 triggering widespread vegetation shifts via woody plant mortality.

62 ainst a reference ITS database developed for woody plants of the region.

63 identification of D14 homologs in the model woody plant Populus trichocarpa.

64 em-differentiating xylem (SDX), in the model woody plant Populus trichocarpa.

65 ted ChIP in wood-forming tissue of the model woody plant Populus trichocarpa.

66 we find grasses growing in the understory of woody plants; rather, other stresses, such as excessive

67 Although the heartwood of woody plants represents the main source of fiber and sol

68 of optimal stomatal behavior, exemplified by woody plants shifting along a continuum of these strateg

69 fforestation processes and invasion by alien woody plants, significantly incresed.

70 e fractional covers of bare soil, grass, and woody plants so as to influence the accessibility of sha

71 ts, it comes at the rapidly accruing cost of woody plant species adapted to the open savanna environm

72 values into mean Delta(leaf) values for 334 woody plant species at 105 locations (yielding 570 speci

73 ed, but that the richness of endemic savanna woody plant species declines with carbon storage both at

74 We show that total woody plant species diversity increases with carbon stor

75 ps in the Brazilian Cerrado by analyzing how woody plant species richness changed with carbon storage

76 cipitation loss using a relationship between woody plant species richness, water and energy regimes.

77 timing and sensitivity to temperature for 43 woody plant species.

78 rsity across a soil-resource gradient for 38 woody-plant species in a temperate forest.

79 to study this wheat oxalate oxidase gene in woody plants, the expression of this gene and the functi

80 In woody plants, these transitions can be separated by year

81 stomatal regulation of leaf gas-exchange of woody plants, thus influencing energy fluxes as well as

82 s is constituted of xylem cells that make up woody plant tissue.

83 es encoding enzymes involved in digestion of woody plant tissues or detoxification of plant alleloche

84 The response of woody plant tissues to freezing temperature has evolved

85 ling for sampling effects, beta-diversity of woody plants was similar and higher than expected by cha

86 ing 835 inventories covering 4660 species of woody plants, we show marked floristic turnover among in

87 Woody plants were two or four times more likely to have

88 l carbohydrates (NSCs) of distal branches in woody plants with contrasting water use strategy.

89 s are among the most destructive diseases of woody plants worldwide.

90 leaf-level trend that has been observed for woody plants worldwide.