ライフサイエンスコーパス: water deficit

1 ty (higher local rainfall and lower climatic water deficit).

2 hanced tolerance of the transgenic plants to water deficit.

3 Stomatal closure is generally induced by water deficit.

4 ific expression patterns were not changed by water deficit.

5 t on ABA signalling in the plant response to water deficit.

6 es including salt stress, osmotic stress and water deficit.

7 a precipitation-induced decline in climatic water deficit.

8 re shifting downslope to maintain a constant water deficit.

9 ontrol of photosynthesis during growth under water deficit.

10 Dalpha3 alter plant response to salinity and water deficit.

11 manner in response to ABA, high salinity and water deficit.

12 d from completing germination by dormancy or water deficit.

13 can execute growth arrest when challenged by water deficit.

14 hic seedling is arrested under conditions of water deficit.

15 l and molecular mechanisms to survive severe water deficit.

16 mperature or in detached leaves subjected to water deficit.

17 scription in response to low temperature and water deficit.

18 ect wall extensibility maintain growth under water deficit.

19 le in adapting plant growth to conditions of water deficit.

20 f TF networks involved in plant responses to water deficit.

21 erant maize and for modeling grain yields in water deficit.

22 ain abortion causes large yield losses under water deficit.

23 plants also displayed enhanced tolerance to water deficit.

24 concentration or leaf water potential under water deficit.

25 sponses of the growth of different organs to water deficit.

26 a results in enhanced performance under soil water deficits.

27 cid and impaired stomatal closure induced by water deficits.

28 y pertain to warmer ecosystems with periodic water deficits.

29 acks, longer growing seasons, and associated water deficits.

30 epair are not routine and mainly occur under water deficits.

31 otypically similar responses to various soil water deficits.

32 case of carbon shortage or under very severe water deficits.

33 Under water deficit (50% of soil water-holding capacity), tota

34 : the response of isoprene emission to plant water deficit; a possible relationship between concentra

35 idopsis (Arabidopsis thaliana) to concurrent water deficit (abiotic stress) and infection with the pl

36 Notably, mean annual climatic water deficit and elevation were not associated with pin

37 The responses of growth to soil water deficit and evaporative demand share an appreciabl

38 large consequences for plant modeling under water deficit and for the design of breeding programs.

39 ollowed over 25 to 30 d under four levels of water deficit and in four hybrids in two experiments.

40 to sample ordered structures because milder water deficit and macromolecular crowding induce high al

41 cutin monomer amount (by 65%), whereas both water deficit and NaCl altered the proportional amounts

42 as activated in response to a combination of water deficit and nematode stress, with 50 specifically

43 -resistance (i.e., lower transpiration(min), water deficit and SLA), but these trends were most clear

44 onian forests spanning gradients in seasonal water deficit and soil fertility.

45 Silk growth rate decreased in water deficit and stopped 2 to 3 d after first silk emer

46 BADH1 and BADH15 mRNA were both induced by water deficit and their expression coincided with the ob

47 acids in leaves and nodules increased during water deficits and coincided with a decline in N2 fixati

48 ; ATHB7 and ATHB12, both strongly induced by water-deficit and abscisic acid (ABA).

49 ryza sativa) cultivars to high temperatures, water deficit, and agricultural field conditions by syst

50 riven stresses such as extreme temperatures, water deficit, and ion imbalance are projected to exacer

51 The signals mediating the WUE response under water deficit are not fully elucidated but involve the p

52 Regional warming and consequent increases in water deficits are likely contributors to the increases

53 growth, indicating possible seasonal climate water deficit as a constraint on growth.

54 ing strong support for leaf vulnerability to water deficit as an index of damage under natural drough

55 itions into six scenarios of temperature and water deficit as experienced by maize (Zea mays L.) plan

56 re is a rapid vegetation reaction as soon as water deficits below normal conditions occur.

57 after stomatal closure (transpiration(min)), water deficit (% below turgid saturation), and specific

58 rences in functional strategies to cope with water deficit between resprouters (dehydration avoiders)

59 duction of at least a few viable seeds under water deficit but causes major yield loss.

60 Water deficit, but not NaCl, increased leaf cuticle thic

61 GPP) has a simple relationship with seasonal water deficit, but that (ii) site-to-site variations in

62 berellin (GA) lead to increased tolerance to water deficit, but the underlying mechanism is unknown.

63 robably because plants are able to withstand water deficits, but they lack the rapid response of arid

64 idday leaf water potential (PsiM) under soil water deficit by closing their stomata, anisohydric spec

65 During dry periods, soil-water deficit can limit evapotranspiration, leading to w

66 Soil water deficit can reduce plant survival, and is likely t

67 Water deficit caused by global climate changes seriously

68 as the relative change in trait value under water-deficit compared with control conditions.

69 f mechanisms that regulate root growth under water deficit conditions and highlights the spatial diff

70 to, pea and sunflower - were evaluated under water deficit conditions in order to associate the diffe

71 d progeny in primary roots under control and water deficit conditions simulated by polyethylene glyco

72 During water deficit conditions, the transgenic plants displaye

73 played SPE complementation under control and water deficit conditions.

74 ional quality of wheat under both normal and water deficit conditions.

75 274 indica genotypes grown under control and water-deficit conditions during vegetative growth, we ph

76 Hence, we propose that, under moderate water deficits corresponding to most European drought sc

77 rns to survive severe drought, but prolonged water deficit, coupled with insect damage, may hamper fr

78 e climate [i.e. 35-year mean annual climatic water deficit (CWD)] and competition (i.e. tree basal ar

79 ure, actual evapotranspiration, and climatic water deficit (deficit) over the contiguous US during th

80 Studies of water deficit, dehydration, salt, and other osmotic stre

81 A comparative transcriptome analysis of soil water deficit drought stress treatments revealed the sim

82 ially under abiotic constraints such as soil water deficit (drought [D]) and high temperature (heat [

83 apid dehydration following desubmergence and water deficit during drought.

84 est in western Amazonia experienced a strong water deficit during the dry season of 2005 and a closel

85 ronments in the glasshouse, contrasting soil water deficit, elevated temperature and their interactio

86 4)CO2 pulse-chase experiments confirmed that water deficit enhanced carbon (C) export to the roots, a

87 hopeiensis exhibits exceptional tolerance to water-deficit environments and is therefore an excellent

88 The water-deficit equation {WD(1) = 0.6 x B(m) x [1 - (140 /

89 In response to water deficit, glycine betaine levels increased 26-fold

90 The sensitivity of expansive growth to water deficit has a large genetic variability, which is

91 ion in soybean (Glycine max) L. Merr. during water deficits has been associated with increases in ure

92 With increasing climatic water deficit, higher propagule pressure (i.e., smaller

93 en exceeds water intake, resulting in a body water deficit (hypohydration) and electrolyte losses.

94 , and we suggest that the persistence of the water deficit (i.e., the drought time-scale) could be pl

95 Water deficit impairs growth, leading to sugar accumulat

96 Our findings suggest that critical water deficits impeding tissue growth occurred at relati

97 ncreasing occurrence of high temperature and water deficit in both agricultural production systems an

98 en genotypes of peach, and also inducible by water deficit in cv. Rio Oso Gem.

99 on with the differential growth responses to water deficit in different regions of the elongation zon

100 If global warming amplifies water deficit in drought-prone areas, tree populations l

101 The deep-water deficit in NO(3)(-) was in near-stoichiometric bal

102 though all species respond similarly to leaf water deficit in terms of enhanced levels of ABA and clo

103 r polyethylene glycol in culture media or by water deficit in the soil.

104 perature effect to the historic frequency of water deficit in the southwestern United States predicts

105 Some of them also accumulate in response to water deficit in vegetative tissues, which leads to a re

106 from uncertainty in the stomatal response to water deficits in soil and atmosphere.

107 Of these treatments, only water deficit increased the total cutin monomer amount (

108 ngly, bos1 plants have impaired tolerance to water deficit, increased salinity, and oxidative stress.

109 A) has been implicated as a key component in water-deficit-induced responses, including those trigger

110 f which were shown in previous studies to be water-deficit inducible.

111 For this purpose, progressing soil water deficit is communicated from roots to shoots.

112 Water deficit is one of the main abiotic factors that af

113 Dehydration (body water deficit) is a physiologic state that can have prof

114 When exposed to root-zone water deficits, line sp12 showed an increase in xylem AB

115 st subjected to a 100-millimeter increase in water deficit lost 5.3 megagrams of aboveground biomass

116 ayed onset of wilting in plants experiencing water deficit, lower transpiration rates, and improved w

117 , suggesting that prevalent conditions under water deficit modulate their conformation.

118 these proteins opens the question of whether water deficit modulates their conformation and whether t

119 It is maximum for water deficits occurring during flowering in maize (Zea

120 kingdom that participate in the tolerance to water deficit of different plant species.

121 The effects of water deficit on BADH mRNA expression, leaf water relati

122 The effects of water deficit on carbon and nitrogen metabolism were inv

123 to investigate the effects of end of season water deficit on phenolic content in drought tolerant an

124 were significantly up-regulated in leaves of water deficit plants, in accordance with the increase in

125 During water deficit, plants produce elevated levels of abscisi

126 Under water deficit, plants reduce transpiration and are able

127 These data demonstrate that, during water deficit, plants respond to growth limitation by al

128 -induced modifications in plant responses to water deficit remain obscure.

129 In total, 152 water deficit-responsive proteins were identified and ca

130 ated in response to diverse stresses such as water deficit, root-knot nematode (RKN) infection, and U

131 pment and in vegetative tissues subjected to water deficit, salinity, low temperature, or abscisic ac

132 for 2 y under well-watered and moderate soil water deficit scenarios.

133 ptation of maize (Zea mays) primary roots to water deficit showed that cell elongation is maintained

134 s experiencing greater increases in climatic water deficit since the 1930s, based on a hydrologic mod

135 s (Arabidopsis thaliana) plants subjected to water deficit, sodium chloride (NaCl), or abscisic acid

136 Dehydration largely refers to intracellular water deficits stemming from hypertonicity and a disturb

137 NA clone (lp3) from loblolly pine induced by water deficit stress (WDS) has been isolated.

138 rice cultivars with contrasting responses to water deficit stress and wheat cultivars well adapted to

139 Expression of the pLP6 gene is repressed by water deficit stress and wounding.

140 ater scarcity and the increasing severity of water deficit stress are major challenges to sustaining

141 tivity to ABA and to reduce water loss under water deficit stress but had no effect on leaf size.

142 , rice growth is seriously constrained under water deficit stress compared with other dryland cereals

143 fferent positions along the nodal root under water deficit stress in wheat, whereas they were relativ

144 wild-type plants under normal conditions and water deficit stress indicated that over-expression of A

145 greater amounts of water during the imposed water deficit stress, resulting in a more favorable plan

146 6PDH gene expression is affected by cold and water deficit stress.

147 d recovery of plants from an episode of soil water deficit stress.

148 ys) development is particularly sensitive to water deficit stress.

149 stomatal conductance and rapid wilting under water deficit stress.

150 lasticity, unlike wheat cultivars exposed to water deficit stress.

151 isition strategy through thinner roots under water deficit stress.

152 d respiratory demand treatment slowed as the water-deficit stress increased.

153 he genetic control of rooting behavior under water-deficit stress is essential to breed climate-robus

154 mand can be used as a sensitive indicator of water-deficit stress responses.

155 We predicted 296 (control), 284 (water-deficit stress), and 233 (plasticity) a priori can

156 control conditions, 106 were detected under water-deficit stress, and 76 were detected for trait pla

157 bundance maintained PS levels in response to water-deficit stress, while 40% showed impaired ribosome

158 metabolism (CAM) when exposed to salinity or water-deficit stress.

159 ion, SLW1 and SLW3 RNAs were abundant during water-deficit stress.

160 idation, can help improve rice adaptation to water-deficit stress.

161 patial scales enables plants to acclimate to water-deficit stress.

162 f homeostasis and translation of mRNAs under water-deficit stress.

163 in nonstressed cotton at sunrise compared to water-deficit stressed cotton, potentially predisposing

164 nscripts in the roots was lower than that of water deficit-stressed seedlings.

165 Water-deficit stresses preferentially reduce shoot growt

166 robic methanogen to study the acclimation of water-deficit stresses which de novo synthesize betaine

167 cotton (Gossypium hirsutum) source leaves to water-deficit stresses.

168 eters of transgenic plantlets subjected to a water deficit suggested that plants from line TS4T8An di

169 PLDdelta rendered plants less responsive to water deficits than the wild type.

170 ss-of-function mutations result in increased water deficit tolerance and higher integrated WUE by red

171 The water deficit tolerance of two HbCuZnSOD over-expressing

172 ntially more stable to expression changes by water deficit treatment than other genotype-specific exp

173 Exogenous ureides applied to the soil and water-deficit treatments inhibited N2 fixation by 85% to

174 L.) as a global food crop and the impact of water deficit upon grain yield, we focused on functional

175 ion to the tolerance of transgenic plants to water deficit was also supported by the increase in tran

176 ne (pLP6) of a gene which is repressed under water deficit was isolated from a loblolly pine (Pinus t

177 western US show that high pre-fire climatic water deficit was related to increased post-fire tree mo

178 Acclimation to water deficit (WD) enables plants to maintain growth und

179 sent a revised aridity index for quantifying water deficit (WD) in terrestrial environments using too

180 relate to spatial and temporal variation in water deficit, we analyze data from three forest dynamic

181 atform with contrasting temperature and soil water deficit, we determined the periods of sensitivity

182 showed that annual rainfall and accumulated water deficit were the main drivers of the distribution

183 rocesses, determines the sink strength under water deficit, whereas photosynthesis determines source