ライフサイエンスコーパス: acclimation

1 e, TtTue1, suggests a potential link to cold acclimation.

2 eins exhibiting altered abundance after cold acclimation.

3 roductive benefits and costs of cadmium (Cd)-acclimation.

4 r proper plant development and environmental acclimation.

5 ogen attack and also exhibit defects in cold acclimation.

6 er to accommodate necessary rumen microbiome acclimation.

7 d forest biomass through either mortality or acclimation.

8 aling pathway plays a key role in plant cold acclimation.

9 y of microtubule organization during drought acclimation.

10 mportance of PSII assembly factors for light acclimation.

11 e-zero temperatures in a process termed cold acclimation.

12 ire and expression of genes involved in salt acclimation.

13 eceptor required for complementary chromatic acclimation.

14 rios explaining their possible roles in cold acclimation.

15 ion increases, although partially lowered by acclimation.

16 n (R) each month at 25 degrees C to quantify acclimation.

17 insight into the diversity of microbial salt acclimation.

18 Also, hit1 mutants are impaired in UV-B acclimation.

19 ead to either programmed cell death (PCD) or acclimation.

20 al, and stomatal responses; as well as plant acclimation.

21 al status) were conducted upon 14-17 days of acclimation.

22 in metamorphosis and that GHR may mediate SW acclimation.

23 ole of sustained CEF in high-salinity stress acclimation.

24 improvement of the lettuce response to cold acclimation.

25 d photoperiod regulate the induction of cold acclimation.

26 naling events that lead to systemic acquired acclimation.

27 to the restricted plant growth and microbial acclimation.

28 riod of 74 days, following 53 days of sludge acclimation.

29 neglect or substantially underestimate light acclimation.

30 ress, which otherwise interfered with stress acclimation.

31 A three-week hypoxia acclimation (48 mmHg) resulted in significant up-regulat

32 tion of such sunflecks are too small to make acclimation a viable strategy in terms of carbon gain.

33 t with rare evolutionary innovations in cold acclimation ability structuring plant distributions acro

34 on mechanism underlying the energy intensive acclimation across soils.

35 Rising carbon dioxide, acclimation, adaptation, and migration can influence the

36 However, the contribution of acclimation/adaptation vs species selection differs amon

37 Hormones associated with seawater acclimation (adrenocorticotropic hormone, cortisol and g

38 Here we examined whether short-term cold acclimation also induced such adaptations in 10 metaboli

39 chloroplast is of utmost importance for cold acclimation and acquisition of freezing tolerance.

40 ted to identify key factors involved in cold acclimation and acquisition of freezing tolerance.

41 sorting along taxonomic lines in tandem with acclimation and adaptation at the level of the individua

42 obust quantitative global model representing acclimation and adaptation of photosynthetic temperature

43 We separated temperature acclimation and adaptation processes by considering seas

44 s responsible for photosynthetic temperature acclimation and adaptation using a global dataset of pho

45 Through acclimation and adaptation, plants efficiently utilize r

46 Acclimation and adaptation, which are key to species sur

47 nable contact with omics data sets and allow acclimation and adaptive response at the phenotype level

48 e in both by supplying N to leaf tissues for acclimation and by facilitating compensatory growth foll

49 k of signaling pathways that coordinate cold acclimation and cold hardiness in overwintering conifers

50 le-plant systemic signals in mediating plant acclimation and defense during different abiotic and bio

51 signaling, is essential for successful plant acclimation and defense.

52 steady-state levels during fasting and cold-acclimation and further with anoxia, but disappeared wit

53 12 skeletal muscle cells in response to heat acclimation and heat shock exposure.

54 rvation across species to play roles in heat acclimation and plant development.

55 resent the microbiome's contribution to host acclimation and potentially adaptation, respectively, an

56 teases implicated in cell-signalling, stress acclimation and programmed cell death (PCD) pathways in

57 inked phenomena play crucial roles in winter acclimation and protection.

58 ic and proteomic networks that lead to plant acclimation and survival.

59 lso suggest a possible cross talk between FL acclimation and systemic acquired resistance-like gene e

60 In addition, it demonstrates that plant acclimation and systemic ROS signaling are interlinked a

61 changes in temperature and light during cold acclimation and the development of cold hardiness, but t

62 hat the rate of warming may impact microbial acclimation and the rate of carbon-dioxide (CO2 ) and me

63 DF induced unique cold acclimation and vernalization responses characterized by

64 daptation to winter is characterized by cold acclimation and vernalization, which respectively lead t

65 Cold acclimation and winter survival in cereal species is det

66 its and primary production depend on optimal acclimation and/or adaptation to environment.

67 Improving the responsiveness, acclimation, and memory of plants to abiotic stress hold

68 vity level) were conducted upon 7-13 days of acclimation, and physiological assays (hypoxia tolerance

69 with induction/initiation, maintenance, cold acclimation, and termination by cold or by photoperiodic

70 has been paid to CEF during long-term stress acclimation, and the consequences of sustained CEF in UW

71 he mechanisms responsible for photosynthetic acclimation are not well understood, effectively limitin

72 dies on the physiological mechanism of plant acclimation are required to better quantify the global d

73 such as wounding, pathogen attack, and cold acclimation, but also drive developmental processes in c

74 the key transcription factors mediating cold acclimation, C-REPEAT BINDING FACTORs (CBFs), interact w

75 Chromatic acclimation (CA) encompasses a diverse set of molecular

76 Cold acclimation (CA) is a well-known strategy employed by pl

77 Consequently, acclimation can confer plasticity in some performance tr

78 irectly compare process-level differences in acclimation capacity among plant types.

79 netic signals in both thermal tolerances and acclimation capacity, although it is weaker in the latte

80 depends on their inherent thermal tolerance, acclimation capacity, and ability for evolutionary adapt

81 verse set of Pooideae species displayed cold acclimation capacity.

82 n with species thermal habitat was found for acclimation capacity.

83 2 generations), which is further evidence of acclimation costs.

84 Photosynthetic temperature acclimation could strongly affect coupled vegetation-atm

85 s were observed between two successive light acclimation cycles, suggesting that the character of the

86 the scope for plasticity resulting from warm acclimation decreased in the Up-selected lines.

87 re interlinked and that the lack of systemic acclimation drives systemic ROS signaling to occur at fa

88 effect usually exceeded the magnitude of the acclimation effect.

89 pe) differences that may have been masked by acclimation effects in the long-term experiment.

90 emperature responses and longer-term thermal acclimation effects.

91 , understanding how complex traits like cold acclimation evolve remains a major challenge in evolutio

92 We integrate acclimation experiments with gene expression analyses to

93 r controlled conditions with subsequent cold acclimation followed by freezing stress.

94 s lacking on the processes of photosynthetic acclimation for colonial algae, although these algae are

95 natomy of the retina reflects adaptation and acclimation for dark and light conditions.

96 ered here is a critical feature of chromatic acclimation for marine Synechococcus worldwide.

97 nowledge gap given the importance of thermal acclimation for plant functioning, both under current an

98 tune their PEB to PUB ratio during chromatic acclimation has not yet been obtained.

99 operating efficiency associated with winter acclimation, highlighting its unique ability to precisel

100 gramming is involved in the response to heat acclimation; however, whether the long-term effects of E

101 on (i.e., a symbiont community shift) versus acclimation (i.e., physiological changes at the molecula

102 heoretical developments to incorporate light acclimation in a TBM.

103 ship among MYB30, the ROS wave, and systemic acclimation in Arabidopsis, the SAA response to HL stres

104 While much is known about photosynthetic acclimation in Arabidopsis, to date there has been no st

105 the phenotype of CI mutants and photoperiod acclimation in Arabidopsis.

106 redox poise as a crucial part of high-light acclimation in C. reinhardtii.

107 Chlamydomonas shows apparent UV-B acclimation in colony survival and photosynthetic effici

108 we explore the evolutionary context of cold acclimation in conifers and evaluate challenges imposed

109 or the incorporation of photosynthetic light acclimation in future models.

110 eed for increased photosystems for low-light acclimation in many phytoplankton.

111 d biosynthesis, a critical component of cold acclimation in other cold-adapted plant lineages, were e

112 Here, we investigated the evolution of cold acclimation in Pooideae and found that a phylogeneticall

113 showed active photosynthesis with high-light acclimation in the outer diatom layer, and low-light acc

114 ion in the outer diatom layer, and low-light acclimation in the underlying cyanobacterial part.

115 Changes in the response of NPQ to light acclimation in WT and mutant plants were observed betwee

116 Acclimation increases tolerance to stress in individuals

117 d-to-high latitudes due to the physiological acclimation-induced reduction in evaporative cooling and

118 bre-type switch in skeletal muscle, and cold acclimation induces beige adipocyte biogenesis in adipos

119 ovide evidence for the widely held view that acclimation is costly and are important for investigatin

120 Such photosynthetic light acclimation is not typically incorporated into models, d

121 Counterintuitively, autumn cold acclimation is triggered not only by exposure to low tem

122 gulators named FciA (for type four chromatic acclimation island) and FciB plays a central role in con

123 ponse decreases R p for mid-latitudes, while acclimation lowers this for the tropics with increases e

124 corals and with increased sedimentation this acclimation may support further transitions to sponge do

125 hrough reducing FAD3 expression is likely an acclimation mechanism to heat stress in peanut.

126 global photosynthesis and possess efficient acclimation mechanisms to cope with nutrient stress.

127 low water-potential controls many downstream acclimation mechanisms.

128 complementing current photosynthetic thermal acclimation models that do not account for T sensitivity

129 If such dampening effects of leaf thermal acclimation occur generally, the increase in respiration

130 encoded by At4g02530) is required for growth acclimation of Arabidopsis thaliana plants under control

131 ly quantified, varied upon long-term (weeks) acclimation of Arabidopsis to low (LL), moderate (ML) an

132 that: (1) incorporating seasonal temperature acclimation of basal photosynthetic capacity improves th

133 hlamydomonas AOX proteins can participate in acclimation of C. reinhardtii cells to excess absorbed l

134 The typical LD acclimation of carbon and nitrogen assimilation as well

135 e activity plays a central role in the rapid acclimation of chloroplast metabolism to ever-fluctuatin

136 ver single factor acclimation scenarios; (3) acclimation of Ea should be restricted to the temperatur

137 Our results show widespread light acclimation of ecosystem photosynthesis.

138 We documented homeostatic respiratory acclimation of foliar and whole-crown respiration rates;

139 llectively, the results suggest: (1) thermal acclimation of leaf R is common in most biomes; and (2)

140 Acclimation of leaf respiration per degree temperature c

141 Thermal acclimation of leaf, stem, and root respiration moderate

142 Understanding of the extent of acclimation of light-saturated net photosynthesis (An )

143 her rates of respiration, even with complete acclimation of maintenance respiration.

144 nal changes in carbon fluxes and outperforms acclimation of other single factors (i.e., Ea or DeltaS

145 Thermal acclimation of photosynthesis can be modelled as changes

146 etermine whether and how multifactor thermal acclimation of photosynthesis occurs.

147 in several cellular processes, including the acclimation of photosynthesis to environmental cues.

148 optimality theory can be used to predict the acclimation of photosynthetic capacity based on the assu

149 nternal CO2 partial pressure (ci ) alongside acclimation of photosynthetic capacity, (ii) variable de

150 veals that JA plays an important role in the acclimation of plants to a combination of HL+HS.

151 Physiological acclimation of plants to an everchanging environment is

152 us photosynthetic changes resulting from the acclimation of plants to average PPFD over intermediate

153 The acclimation of plants to light has been studied extensiv

154 We further address the role of ROS in the acclimation of plants to stress combination as well as t

155 Here we propose that the acclimation of R(d) follows an optimal behaviour related

156 ynthetic co-ordination theory to predict the acclimation of R(d) to growth temperature via a link to

157 During this time, we detected no acclimation of respiration rates, no thermal compensatio

158 le of entire trees, suggesting that complete acclimation of respiration to warming is likely to dampe

159 to affect the timing, magnitude, and thermal acclimation of soil carbon loss.

160 experimental warming have documented thermal acclimation of soil respiration involving adjustments in

161 tochondrial and chlororespiration during the acclimation of stm6 and the MOC1-complemented strain to

162 for 2050 and accounting for possible thermal acclimation of Tcrit and Tmax , we also found that these

163 These results suggest that temperature acclimation of the biochemical processes that underlie p

164 le they brood their larvae, or developmental acclimation of the larvae inside the adult polyps, may p

165 We assessed short-term (7 day) temperature acclimation of the maximum rate of Rubisco carboxylation

166 Consequently, IsaR1 affects the acclimation of the photosynthetic apparatus to iron star

167 i (HpalphaCA) plays an important role in the acclimation of this oncobacterium to the acidic pH of th

168 criptional patterns and morpho-physiological acclimations of Brachypodium dystachion to single salini

169 The cold acclimations of mesophyll conductance (g(m) ), bundle-sh

170 that terminate the SnRK2s signal relay after acclimation or post-stress conditions remain to be defin

171 did not change in position or intensity with acclimation period or temperature.

172 A 10-day cold acclimation period resulted in increased cold-induced gl

173 tages of tight paper-packed structure, short acclimation period, high power output, and high sensitiv

174 e the observed differences between the light acclimation periods.

175 Photosynthetic acclimation (photoacclimation) is the process whereby le

176 ced systemic signaling and systemic acquired acclimation play canonical roles in plant survival durin

177 rganisms, yet we lack understanding of their acclimation potential in the natural environment.

178 educed photosynthesis, whereas physiological acclimation prevented a coincident increase in Ra .

179 oxygen species (ROS) play a key role in the acclimation process of plants to abiotic stress.

180 In this study, we investigated the acclimation process of the alga to a colder temperature

181 s that are essential for plant viability and acclimation processes.

182 cate ROS and redox signature, which controls acclimation processes.

183 ranscription factor essential for plant cold acclimation, promotes hypocotyl growth under ambient tem

184 ctor scenarios of photosynthetic temperature acclimation provide minimal (if any) improvement in mode

185 ate (A(max)), with croplands having stronger acclimation rates than grasslands and forests.

186 ated within the context of realistic thermal acclimation regimes and potential anthropogenic climate

187 This suboptimal acclimation renders a large portion of residual photosyn

188 Quantitative proteomics revealed that acclimation requires, besides remodeling of the photosyn

189 atures that determine the specificity of the acclimation response and help tailor it to the exact str

190 Blue rockfish had a lower pCrit and stronger acclimation response compared to copper rockfish.

191 and ERF103 is also required for a full cold acclimation response likely involving the CBF regulon.

192 Rubisco abundance that underpin the thermal acclimation response of photosynthesis in wet-forest tre

193 to WD Interestingly, the morphophysiological acclimation response to WD also was reflected in the gen

194 to improve plant water-use efficiency as an acclimation response.

195 o adjust their metabolism and mount a proper acclimation response.

196 ectly regulate gene expression necessary for acclimation responses in plants.

197 The acclimation responses observed here suggest that warmer

198 We discuss possible causes of the different acclimation responses of C. reinhardtii and B. braunii K

199 Thermal acclimation responses of carbon metabolic processes can

200 reversal following N resupply and uncovered acclimation responses specific to the recovery phase.

201 ross-development phenotypic correlations for acclimation responses suggest that plasticity itself may

202 The adaptation and acclimation responses that allow some insects to tolerat

203 well as play a critical role in defense and acclimation responses to different biotic and abiotic co

204 Similarly, hypoxia acclimation resulted in a 20% reduction in whole animal

205 Systemic signaling and systemic acquired acclimation (SAA) are essential for plant survival durin

206 Systemic acquired acclimation (SAA) is a key biological process essential

207 Systemic acquired acclimation (SAA) plays a key role in optimizing growth

208 the ability of 66 photosynthetic temperature acclimation scenarios to improve the ability of a spatia

209 ment in model performance over single factor acclimation scenarios; (3) acclimation of Ea should be r

210 clustering analysis of morpho-physiological acclimations showed that several traits exhibited a grad

211 ever, both the role of LCI1 in various CO(2) acclimation states and the species of C(i) , HCO(3) (-)

212 lay distinct roles in low and very low CO(2) acclimation states.

213 spond to diverse stress conditions, and what acclimation strategies are employed during bloom dynamic

214 Growth inhibition and cold-acclimation strategies help plants withstand cold stress

215 concentrating mechanisms but also change the acclimation strategy of the cells to light.

216 to 43 parts per thousand (ppt), yet its salt acclimation strategy remains enigmatic because the genom

217 Plants employ cold acclimation strategy to protect them from cold damage.

218 The photoprotective acclimation strategy was also contrasting, with LL plant

219 By updating a TBM to include photosynthetic acclimation, successfully reproducing the [Formula: see

220 While acclimation temperature positively affected the upper cr

221 We compared the relative importance of acclimation temperature to changes in upper critical the

222 cross development for either trait at either acclimation temperature.

223 choice to stay in a habitat reflecting their acclimation temperatures or relocate, fish acclimated to

224 pid metabolism, known to be involved in cold acclimation, tended to show consistent regulation in bot

225 Photosynthetic acclimation, the ability to adjust the composition of th

226 Without acclimation, the DeltaC(a)-driven boost in net primary p

227 With acclimation, the DeltaC(a)-driven boost in NPP and stand

228 During cold acclimation, the properties of the chloroplast change ma

229 en species can also act as signals to induce acclimation through chloroplast degradation, cell death

230 rming resulted in significant changes across acclimation time.

231 rate was varied to determine the impacts of acclimation time.

232 d lower-latitude hosts generally have slower acclimation times than smaller and higher-latitude hosts

233 se their bleaching thresholds after 6-months acclimation to + 1 degrees C warming.

234 tain their heat tolerance and health despite acclimation to 3-6 degrees C cooler, more stable tempera

235 ENOSA4 (VEN4) in chloroplast development and acclimation to adverse growth conditions.

236 We show that failing to account for acclimation to antecedent environment or coordination wi

237 n to climate, and temporally, as a result of acclimation to changes in ambient temperature.

238 crop plant soybean and could be involved in acclimation to changes in light conditions occurring in

239 ties may serve as a mechanism of rapid coral acclimation to changing environmental conditions.

240 Acclimation to changing light intensities poses major ch

241 insights into molecular changes during fruit acclimation to cold environment.

242 eme heat and cold stress after developmental acclimation to cool (18 degrees C) and warm (25 degrees

243 We modeled stands with and without acclimation to DeltaC(a) and DeltaT, where acclimated fo

244 etic light response curves but also by plant acclimation to dimming that gradually increased leaf nit

245 ate the mechanisms underlying photosynthetic acclimation to elevated temperature and carbon dioxide (

246 response to abiotic stress to mediate plant acclimation to environmental challenge.

247 xes can decouple, and provide no evidence of acclimation to environmental change at a decadal timesca

248 These responses allow acclimation to fluctuating light conditions, e.g. sunfle

249 hown to move to the nucleus to promote plant acclimation to fluctuating light.

250 e information by signalling to nuclei during acclimation to fluctuating light.

251 Our findings highlight the impact of acclimation to future climates on predictions of carbon

252 ticity have been identified as mechanisms of acclimation to global change, the weight of evidence ind

253 We found acclimation to growth temperature to be a stronger drive

254 We observe that plant tolerance and acclimation to heat shock vary throughout the day and ar

255 Traditionally, acclimation to high CO(2) has been considered in terms o

256 uction-oxidation processes play key roles in acclimation to high CO(2), with specific enzymes acting

257 n of a single chloroplast gene, psbA, during acclimation to high light.

258 mic transcriptomic responses, SAA, and plant acclimation to HL stress.

259 tsH1/3 complex is of critical importance for acclimation to iron, phosphate, carbon, and nitrogen sta

260 TBMs), to quantify and assess photosynthetic acclimation to light in natural environments.

261 While the mechanisms of long-term acclimation to light intensity have been studied by chan

262 sfer and its regulation during developmental acclimation to light intensity.

263 ing mechanism (CCM) that helps in successful acclimation to low CO(2) conditions.

264 ess-Activated RNA 1) plays a pivotal role in acclimation to low-iron conditions.

265 is study, the natural variation of long-term acclimation to moderate and severe soil WD was investiga

266 CfrA in the adaptation of carbon flux during acclimation to nitrogen deficiency.

267 of SSP gene families potentially involved in acclimation to nutrient deficiencies and nodulation.

268 ere were no indications of transgenerational acclimation to ocean acidification during experiments.

269 ng fluid chemistry implies the potential for acclimation to ocean acidification.

270 cus strains use a process known as chromatic acclimation to optimize the ratio of two chromophores, g

271 g protein, show a specific effect of drought acclimation to promote splicing efficiency of IR-prone i

272 Acclimation to realistic daily heat pulses enhanced ther

273 H(2) O(2) in signalling, for example during acclimation to stress and pathogen defence, has received

274 hat regulate different pathways during plant acclimation to stress, but are also toxic byproducts of

275 al peat swamp forest in the absence of plant acclimation to such changes in atmospheric dryness.

276 Altogether, our results show that acclimation to temperature and CO(2) is primarily relate

277 ovide a parsimonious general theory for R(d) acclimation to temperature that is simpler-and potential

278 ting that TPP also plays a role in metabolic acclimation to the photoperiod.

279 hnia pulex, we isolated the contributions of acclimation to the regulation of the metal response gene

280 function of weight, and did not improve with acclimation to the system.

281 g a specific set of genes that contribute to acclimation to this unfavorable environmental condition.

282 ncodes diverse phenotypic traits that permit acclimation to varied microenvironmental conditions.

283 Rd acclimation to warmer temperatures caused a reduction in

284 In general, acclimation to warmer temperatures increased the rate of

285 ommon across different plant types, but that acclimation to warmer temperatures tends to have a relat

286 Acclimation to water deficit (WD) enables plants to main

287 into quantitative aspects of cyanobacterial acclimations to different growth rates have implications

288 f community effects as temperatures exceeded acclimation values.

289 fundamental role for VRN1 in regulating cold acclimation, vernalization, and morphological developmen

290 ncrease in respiration with temperature, but acclimation was constrained at high temperatures.

291 Hypoxia acclimation was not associated with changes in gill morp

292 Rd acclimation was similar across plant types.

293 The extent of thermal acclimation was tested by monitoring CO2 and CH4 product

294 Among other physiological acclimations, we identify an upregulation of the transla

295 One such adaptation is cold acclimation, wherein plants increase their frost toleran

296 otosynthetic apparatus in the first 250 h of acclimation, which was followed by cell growth to an eve

297 Understanding physiological acclimation will be critical for the large carbon stores

298 shift their distribution, and the limits of acclimation will likely be tested by climate change in t

299 nd of the day, indicating interactions of FL acclimation with leaf development stage and time of day.

300 These findings support the hypothesis that acclimation within individuals, adaptation within specie