ライフサイエンスコーパス: water stress

1 maturation depending on the duration of the water stress.

2 isition, and improved growth and yield under water stress.

3 fluctuations of uptake rates in response to water stress.

4 lant's control of stomatal conductance under water stress.

5 d to apply irrigation to cope with increased water stress.

6 en isotope ratio of plants under salinity or water stress.

7 isition, and improved growth and yield under water stress.

8 abscisic acid (ABA) to close stomata during water stress.

9 ests, but fail to capture their responses to water stress.

10 ABA levels to close stomata during sustained water stress.

11 tive to the wild-type wheat genotypes during water stress.

12 , and attenuates derepression of genes under water stress.

13 n suggests an increasing frequency of lethal water stress.

14 wth control in the plant response to ROS and water stress.

15 ase of compounds related to the avoidance of water stress.

16 dogenous ABA and leaf water potential during water stress.

17 crop quality under artificially imposed mild water stress.

18 s in plants subjected to different levels of water stress.

19 st in postgermination embryos that encounter water stress.

20 l for plants experiencing dynamic changes in water stress.

21 al properties of these macromolecules during water stress.

22 eus, and its expression was downregulated by water stress.

23 ons of LEA proteins in animal species during water stress.

24 tic processes and its beneficial role during water stress.

25 ditions in which the crop did not experience water stress.

26 el tissues in developing maize kernels under water stress.

27 ponse of rice (Oryza sativa) gas exchange to water stress.

28 atible solutes (osmolytes) in acclimation to water stress.

29 uction of photosynthesis under conditions of water stress.

30 d roots and is strongly induced in leaves by water stress.

31 and found that it is induced specifically by water stress.

32 His1-1, His1-2 and His4 appear unaffected by water stress.

33 n dark-induced senescence and in nutrient or water stress.

34 ing bubbles in the stem xylem during imposed water stress.

35 ts evolved different strategies to cope with water stress.

36 ss would add considerably to drought-related water stress.

37 t parts and alternative methods for inducing water stress.

38 ing photosynthesis is strongly influenced by water stress.

39 clines, presumably because of leaf ageing or water stress.

40 t of abscisic acid, which is associated with water stress.

41 ht and implying that mitigation would reduce water stresses.

42 Soybean plants were not visibly nutrient- or water-stressed.

43 All species were very vulnerable to water stress (50% reduction in whole-leaf hydraulic cond

44 een and Purple Iranian), and the impact that water stress (75% and 50% field capacity) and storage ti

45 When detached bean leaves were water stressed, ABA accumulation was preceded by large i

46 widespread ant-plant symbiosis increase with water stress across 26 sites along a Mesoamerican precip

47 e CO2 effects on WUE in the model alleviated water stress across all sites.

48 esults, to summarize expression responses to water stress across studies, and meta-regression to mode

49 The wheat translocation line had improved water stress adaptation and higher root and shoot biomas

50 its are an important component for improving water stress adaptation.

51 Given the current replacement of water-stress adapted 'xerophytic' tree species by mesoph

52 r-stress treatment caused more embolism than water stress alone.

53 ed ancestry or independent associations with water stress alone.

54 Plant hydraulics integrated water stress along the soil-plant continuum and was more

55 Moderate water stress also increased beta-carotene, flavonoids an

56 world's population is currently experiencing water stress and (ii) rising water demands greatly outwe

57 esh of interconduit pit membranes during the water stress and cavitation treatment.

58 ontrolled to enable plant protection against water stress and define the dimeric receptors as key tar

59 With growing water stress and demand for energy, this number will con

60 e crucial for heavy use, factors relating to water stress and geographical proximity matter most for

61 ggested to act as an osmosensor that detects water stress and initiates downstream responses.

62 ons but that grasses are more susceptible to water stress and lose biomass more quickly in dry condit

63 s located in Nebraska, a state with moderate water stress and moderate corn production (11%).

64 2011, and examined the relationship between water stress and NDVI.

65 Tolerance to water stress and salinity was evaluated using calli and

66 s of mannitol in wheat improves tolerance to water stress and salinity.

67 spiration could be primarily attributable to water stress and subsequently limited plant growth (comm

68 eal macrophages is also increased after cold water stress and that the peptide substance P (SP) parti

69 of carbohydrates in roots and stems, during water stress and the rapid disappearance upon rewatering

70 e differences among models in sensitivity to water stress and, among the N cycle models, N availabili

71 osynthetically active zones when the leaf is water stressed and under high-light and low CO(2) condit

72 n by an external environmental factor, 'soil water stress' and consequently by a constant or decreasi

73 attern consistent with warming and increased water stress, and also with paleohistoric shifts in vege

74 r relation traits can acclimate to long-term water stress, and highlight the limitations of extrapola

75 To overcome heat, water stress, and increased exposure to ultraviolet radi

76 ture forests; interactions with temperature, water stress, and phosphorus limitation; and the influen

77 ic variables, such as the method of applying water stress, and the part of the plant the mRNA was ext

78 alleviate climate-induced increases in plant water stress, and, as a result, sustain high biomass for

79 gross primary production (GPP) responses to water stress are commonly based on remotely sensed chang

80 wth promotion and root tropic response under water stress are key responses for plant survival under

81 the example of corn grain shows that 59% of water stress associated with corn grain production in th

82 acts of virtual water trade on water use and water stress at both the national and basin level.

83 may cope with and respond to temperature and water stress at the molecular level in distinct ways, wi

84 Cold water stress augments the lipopolysaccharide-induced IL-

85 PaNCED1 was induced by water stress, but expression of PaNCED3 was not detectab

86 are characters often cited as adaptations to water stress, but links between the function of these tr

87 PvNCED1 mRNA and ABA were slowly induced by water stress, but, at 2 degrees C, neither accumulated.

88 range Habanero, and BGH1719 responded to the water stresses, but produced less capsaicinoid yield as

89 ne abscisic acid (ABA) protects seeds during water stress by activating genes through transcription f

90 ow pre-harvest factors, such as grafting and water stress, can influence the phenolic content of toma

91 aceutical and natural steroid estrogens in a water stressed catchment in South Australia alongside a

92 l drought but are likely to face intensified water stress caused by higher temperatures and to be vul

93 itive sudden hydraulic failure under extreme water stress (cavitation).

94 itself may raise questions of constraints in water-stressed cities, with such a shift in Delhi increa

95 fting on specific rootstocks more adapted to water stress conditions may be a tool to improve crop qu

96 So, the richness of ZarxJos under water stress conditions with these compounds confirms it

97 ed better growth when exposed to low-K(+) or water stress conditions.

98 e development of supernumerary carpels under water-stress conditions.

99 mucilage release and seed germination under water-stress conditions.

100 ional area were grown under well-watered and water-stressed conditions in greenhouse mesocosms and in

101 sting CCFN were grown under well-watered and water-stressed conditions in greenhouse mesocosms and in

102 when the lamellar phases were prepared under water-stressed conditions, despite the fact that x-ray-i

103 genes in Pseudomonas putida that are matric water stress controlled and to generate mutants defectiv

104 This study reveals that appropriate water stress could increase capsaicinoid yield in some,

105 water desalination plants have been built in water-stressed countries to augment available water reso

106 f those where there are moderate and greater water stress countrywide (except Italy).

107 Thus, acute water stress damage shows parallels to vacuole-mediated

108 The water stress decreased Mn, P, Mg and S contents in 100,

109 ssimilation by trees at the MMSF, increasing water stress decreased the number of days of wood produc

110 Water stress depleted the volatile profile of these thre

111 forests are projected to experience seasonal water stress, despite anticipated increases in precipita

112 nly after prolonged exposure to more extreme water stress did active ABA-mediated stomatal closure be

113 As trees grow taller, increasing leaf water stress due to gravity and path length resistance m

114 um, but not the lens fibers, protection from water stress during intervals of osmotic crisis.

115 In addition to buffering plants from water stress during severe droughts, plant water storage

116 led tendencies toward lower vulnerability to water stress (e.g. osmotic potential at full turgor, cel

117 Heat but not water stress elevated NCED4 expression in leaves, while

118 Although the early startle response to cold water stress elicited a pressor response in all rats, th

119 d to provide benefit across the diversity of water stress environments relevant to economic yield.

120 agricultural sustainability in nutrient- and water-stressed environments.

121 -habitat Ranunculus lanuginosus Accordingly, water stress-exposed plants from the broad-amplitude Ran

122 otrusion was blocked by abscisic acid (ABA), water stress, far-red light, or dormancy, but was low or

123 contiguous US suggest consistent increase in water stress for power production with about 27% of the

124 104 countries; virtual water trade mitigated water stress for the basins within 85 of the 104 countri

125 frLEA3m and trehalose, exhibit resistance to water stress (freezing) as evidenced by an unchanged cap

126 redicting plant responses to a wide range of water stress from one or two sampled traits, increasing

127 consistent socioeconomics, the reductions in water stress from slower rates of climate change resulti

128 mitigation are overwhelmed by the increased water stress from the emissions mitigation itself.

129 Thirdly, the phenomenological water-stress functions used by the terrestrial biosphere

130 ibers appeared to be unable to cope with the water stress generated by the transgene-induced over-acc

131 In the absence of water stress, growth at elevated [CO2] did not stimulate

132 hytic tree species, we estimate that chronic water stress has the potential to decrease the C sink of

133 ydraulic conductance (Kleaf) with increasing water stress have been attributed to cavitation of the l

134 The region is characterized by water stress, high dessert conditions, declining land he

135 It facilitates responses to drought, to the water stress hormone abscisic acid, and to pathogen atta

136 The influence of the plant water-stress hormone abscisic acid (ABA) on anion channe

137 tribute to signalling cascades evoked by the water-stress hormone abscisic acid (ABA) that lead to st

138 r watersheds account for 78% of the national water stress impact, as these areas have high milk produ

139 as increased by low-temperature exposure and water stress in a manner consistent with a probable func

140 hemodynamic response patterns to acute cold water stress in conscious rats.

141 academics, especially in light of increasing water stress in many regions around the world.

142 2) would also substantially exacerbate plant water stress in marginally arid environments, providing

143 Under water stress in mesocosms, lines with large CCS had betw

144 Overall, with the increase of water stress in plants, the osmotic potential of liquid

145 the ETCW, which is consistent with increased water stress in response to climate warming and dryer so

146 the observed diversity in plant responses to water stress in seasonally dry tropical forests (SDTFs).

147 site with greater cloud cover exhibited less water stress in summer, larger basal area growth, and gr

148 High water stress in T2 delayed fruit maturation, increased a

149 and Pinus contorta) that experienced lethal water stress in the field and in laboratory conditions.

150 Under water stress in the field, genotypes with reduced CCFN h

151 Under water stress in the field, lines with large CCS had betw

152 Under water stress in the mesocosms, genotypes with reduced CC

153 ase in cardiac output elicited by acute cold water stress in vascular responders without affecting mi

154 Although water stress increased and growth declined strongly at l

155 The water stress increased stomatal resistance and decreased

156 Such additional water stress increases the risk of social instability, c

157 approach that relies on a novel multivariate water stress index, which considers the joint probabilit

158 hysical water scarcities can be described by water stress indices.

159 This supports the hypothesis that water stress induced by high temperatures causes the dec

160 Across the deciduous forest region, water stress induced similar declines in tree growth, pa

161 Implications for regulation of water stress-induced ABA biosynthesis are discussed.

162 specific SP antagonist, eliminates the cold water stress-induced augmentation of IL-6 secretion from

163 al cavity, where it participates in the cold water stress-induced macrophage functional alterations.

164 s to a loss of function by cavitation during water stress is a key indicator of the survival capabili

165 A well known response of plants to water stress is accumulation of ABA, which is caused by

166 the C sink due to mesophication and chronic water stress is equivalent to an additional 1-3 days of

167 Our analysis suggests that dry-season water stress is likely to increase in E.

168 Our work suggests that alleviating water stress is not the reason we find grasses growing i

169 between the carbon footprint and the induced water stress is observed.

170 Water stress is one of the primary selective forces in p

171 imate change, and especially drought-induced water stress, is the dominant cause of the observed redu

172 ave high milk production and relatively high water stress; it is the production of local silage and h

173 tory had shown that exposure of mice to cold water stress leads to an increase in the secretion of in

174 We have used 18O2 to label ABA in water-stressed leaves of mutant and wild-type Arabidopsi

175 els were rapidly increased by rehydration of water-stressed leaves.

176 difference vegetation index) indicated that water stress limited GEE and inhibited Reco .

177 Water stress makes this region vulnerable economically a

178 Water stress markedly decreased the grain Se, iron (Fe),

179 tosynthesis and nitrogen assimilation during water stress, neither carbon nor nitrogen assimilation w

180 The water stressed North stays in contrast to the water abun

181 e found, and miRNAs regulated in response to water stress, nutrient stress, or temperature stress wer

182 T3 advanced internal ripening when moderate water stress occurred during the first 40 days of phase

183 When we included the NDVI responses to water stress of adjacent ecosystems with high SSWS into

184 do aspens to the most extreme growing season water stress of the past century by creating high atmosp

185 e mortality, the impacts of mild but chronic water stress on forest phenology and physiology are larg

186 Effect of water stress on germination was tested for fresh and 6-m

187 oved framework for predicting the impacts of water stress on GPP in forests with low SSWS.

188 ral content and to investigate the effect of water stress on it.

189 ther factors seemed to have more impact than water stress on K, Ca, Cu, Fe and Zn levels.

190 examined the effects of light intensity and water stress on metabolism by using a combination of dir

191 bon allocation, phenology, and the impact of water stress on phenology.

192 The effect might be indirect: water stress on plants can lead to carbon stress, which

193 Here, we investigated the effects of cold water stress on the hippocampus of sedentary and runner

194 tomatal conductance during the imposition of water stress on two drought-tolerant conifer species wit

195 grafting) combined with the abiotic stress (water stress) on the content of phenolic compounds (flav

196 We demonstrate that water stress operating at the scale of individual plants

197 Water-stressed Opuntia show decreased ascorbic acid leve

198 vation in response to a period of protracted water stress or temperature-insensitive sudden hydraulic

199 atment effects were subtle and contingent on water stress, phenology, and species composition.

200 (Na2SeO4) improved the yield and quality of water stressed plants due to enhancement in the producti

201 bolism and signaling in roots of flooded and water stressed plants of Carrizo citrange revealed that

202 lly watered (Psi approximately -0.3 MPa) and water-stressed plants (Psi approximately -2 MPa).

203 Upon irrigation, the source leaves of the water-stressed plants recovered to prestress values with

204 enic isoprene, a major ozone precursor, from water-stressed plants under a dry and warm condition.

205 boidea to rapidly recover gas exchange after water-stressed plants were rewatered, and was associated

206 The method is verified in water-stressed plants, as compared with a well-watered t

207 In water-stressed plants, peduncle Psi and crease pericarp

208 To cope with water stress, plants must be able to effectively sense,

209 ystem while avoiding the severe effects that water stress poses on woody species.

210 cleavage enzyme (PvNCED1) is up-regulated by water stress, preceding accumulation of ABA.

211 re affected by biases in factors controlling water stress (precipitation, humidity, and air temperatu

212 quantified tree-to-tree variation in growth, water stress (predawn and midday xylem tension), drought

213 ghted plants, material was not significantly water stressed prior to collection.

214 These results suggest that cold water stress promotes the release of SP from peritoneal

215 Although water stress reduces fruit yield, it also increases caps

216 facilitating plant nutrient acquisition and water stress resistance, arbuscular mycorrhizal (AM) fun

217 tial genetic source in breeding programs for water stress resistance.

218 dence that ATHK1 not only is involved in the water stress response during early vegetative stages of

219 To identify genes induced during the water stress response in Bermudagrass (Cynodon dactylon)

220 erefore also a poor basis for parameterizing water stress response in land-surface models.

221 s a major physiological determinant of plant water stress response.

222 signaling, distinguishing it from a classic water-stress response.

223 to a richer understanding of the biology of water stress responses, and may prove valuable in other

224 ying the cellular signaling events governing water-stress responses, it is also important to consider

225 sults of various studies seeking to identify water stress-responsive genes only partially overlap.

226 We used a water stress-responsive transcriptional fusion to quanti

227 of endophytic bacterial population size, and water stress, resulting from high osmolarity or tissue d

228 o exhibit ABA-driven stomatal closure during water stress, resulting in strongly isohydric regulation

229 in protein profiles between well-watered and water-stressed roots.

230 the apical region of the elongation zone of water-stressed roots.

231 tiated by elevated foliar ABA, but sustained water stress saw a marked decline in ABA levels and a sh

232 as well as novel drought-phenology and plant water stress schemes.

233 ime stomatal closure in response to moderate water stress seemed to be a passive hydraulic process in

234 ought in recorded history, causing statewide water stress, severe economic loss and an extraordinary

235 Interestingly, acute water stress showed accumulation of singlet oxygen as de

236 Under T2, trees suffering moderate water stress showed increased flavonoid and phenolic con

237 nd water demand, the region could experience water stress similar or worse than the epic Millennium D

238 o protein (or protein precursors) of intact, water-stressed soybean leaves exposed to (13)CO(2) and (

239 any forests have low spectral sensitivity to water stress (SSWS) - defined here as drought-induced de

240 When instantaneously rehydrated from a water-stressed state, fern and lycophyte stomata rapidly

241 During water stress, stomatal closure occurs as water tension a

242 rporation of glycine into protein shows that water stress suppresses photorespiration in soybean leav

243 groups of plants with well-defined levels of water stress that could not be detected visually.

244 ofile during storage varied depending on the water stress that had been applied.

245 fecycles, trees encounter multiple events of water stress that often result in embolism formation and

246 Upon water stress, the overexpression of VvPIP2;4N induced a

247 Under water stress, the trees have smaller carbon pools.

248 the delayed decline in fluorescence yield of water-stressed tissue exposed to prolonged elevated resp

249 ne across the range of dehydration from mild water stress to beyond turgor loss point.

250 plants (Populus x canescens) were exposed to water stress to investigate xylem sap sulfate and ABA, s

251 oisture, seasonal and annual streamflow, and water stress) to projections of future climate.

252 overexpression of ATHK1 results in increased water stress tolerance, our observations suggest a new t

253 o determine their role in poplar response to water stress, transgenic Populus tremula x Populus alba

254 In both species, the freeze-thaw plus water-stress treatment caused more embolism than water s

255 ould periodically experience nutritional and water stress under these conditions, and thus the common

256 We quantified the C consequences of chronic water stress using a 13-year record of tree growth (n =

257 decline in N(2) fixation rate in response to water stress was always greater for plants inoculated wi

258 Cell death by acute water stress was inhibited by the singlet oxygen scaveng

259 s affected by the ATHK1-mediated response to water stress, we created a large-scale summary of expres

260 level, the impacts of virtual water trade on water stress were statistically significant for basins a

261 fied, particularly in countries experiencing water stress, where dilution of pollutants entering rive

262 in primary leaves was strongly increased by water stress, whereas PvCYP707A1 and PvCYP707A2 mRNA lev

263 sibly, enabling seedlings to withstand early water stress without loss of viability.

264 cultures of dot/icm mutants in water, termed water stress (WS).

265 to non-NATs are specifically expressed under water stress (WS).

266 tolerance to environmental stresses, such as water stress (WS).

267 rown in environments without (WoWS) and with water stress (WthWS).