ライフサイエンスコーパス: acclimation

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

2 insight into the diversity of microbial salt acclimation.

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

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

5 dipose tissue depots was unchanged upon cold acclimation.

6 ontogenetic changes including hardening and acclimation.

7 trosylation in the context of photosynthetic acclimation.

8 UV RESISTANCE LOCUS8 (UVR8) and induces UV-B acclimation.

9 n a BR- and CES-dependent manner during cold acclimation.

10 rt differentially in response to temperature acclimation.

11 rsensitive to freezing before and after cold acclimation.

12 were determined to investigate mechanisms of acclimation.

13 improvement of this resistance through cold acclimation.

14 ng potential substrate regulation of thermal acclimation.

15 s important during sub-zero than during cold acclimation.

16 mated flies respond positively to short-term acclimation.

17 ae-related bacteria were selected during the acclimation.

18 stered with chronic low-dose LPS before cold acclimation.

19 es into the molecular mechanisms of sub-zero acclimation.

20 s UV-B-induced photomorphogenesis and stress acclimation.

21 bidopsis genes are regulated during sub-zero acclimation.

22 direct electron transfer was enhanced by the acclimation.

23 table variation in both short- and long-term acclimation.

24 on-damaging sub-zero temperatures after cold acclimation.

25 temic signaling leading to systemic acquired acclimation.

26 lator of the gene expression response during acclimation.

27 ezing tolerance were apparent only upon cold acclimation.

28 mportance of PSII assembly factors for light acclimation.

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

30 ire and expression of genes involved in salt acclimation.

31 eceptor required for complementary chromatic acclimation.

32 y of microtubule organization during drought acclimation.

33 ion increases, although partially lowered by acclimation.

34 tive blocks of 1-month overnight temperature acclimation (24 degrees C [month 1] --> 19 degrees C [mo

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

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

37 involvement of the rhodopsin pathway in cold acclimation, a pathway that has been recently linked to

38 severe growth inhibition and perturbed light acclimation, accompanied by strong impairments of Calvin

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

40 rior generations can influence hardening and acclimation, although evidence for the latter remains we

41 TFs may be important regulators of sub-zero acclimation, although the CBF signal transduction pathwa

42 ms, which use both basal thermotolerance and acclimation, an adaptive plastic response, to mitigate t

43 In order to assess the potential for acclimation and adaptation in the honeycomb worm, Sabell

44 threshold for coral bleaching depends on the acclimation and adaptation of corals to the local maximu

45 functional and population genomics of plant acclimation and adaptation to elevated CO2 .

46 Acclimation and adaptation, which are key to species sur

47 y, stress memory may provide a mechanism for acclimation and adaptation.

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

49 analysis of gene expression during sub-zero acclimation and allow the identification of candidate ge

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

51 12 skeletal muscle cells in response to heat acclimation and heat shock exposure.

52 Mild heat acclimation and moderate heat shock appear to have diffe

53 ported that more positive potentials improve acclimation and performance of exoelectrogenic biofilms,

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

55 ignaling in the green lineage to induce UV-B acclimation and protection.

56 quenching becomes activated upon high light acclimation and requires the accumulation of light harve

57 of stress genes implying that long-term cold acclimation and short-term stress response may have a di

58 to mechanisms of thermosensation and thermal acclimation and suggests that rGCs may represent a new f

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

60 r UV RESISTANCE LOCUS 8 (UVR8) promotes UV-B acclimation and tolerance in Arabidopsis thaliana UVR8 l

61 Cold acclimation and winter survival in cereal species is det

62 role of the microbiome in coral resilience, acclimation, and environmental adaptation is a new front

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

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

65 ysiological adjustments arising from thermal acclimation are capable of explaining observed variation

66 Both basal thermotolerance and acclimation are thought to be important for local adapta

67 ts in respiration over time (through thermal acclimation) are consistent with the patterns in R found

68 d Tenela during the first 3 days of sub-zero acclimation at -3 degrees C.

69 duction were gradually increased during cold-acclimation, but unaffected by Cox7a1 knockout.

70 e-green environments using type IV chromatic acclimation (CA4).

71 Consequently, acclimation can confer plasticity in some performance tr

72 Acclimation can occur over longer (seasonal) or shorter

73 owed that the lack of NsiR4 led to decreased acclimation capabilities of Synechocystis toward oscilla

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

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

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

77 pigmentation during complementary chromatic acclimation (CCA) is well studied in Fremyella diplosiph

78 argely consistent with previous work on cold acclimation/cold tolerance.

79 Thermal acclimation could mitigate the expected respiration incr

80 Photosynthetic temperature acclimation could strongly affect coupled vegetation-atm

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

82 ena, i.e. in response to (long-term) drought acclimation (DA) or to (transient) heat stress (HS).

83 reased with increasing leaf temperature, but acclimation did not result in perfect homeostasis of res

84 hat are differentially expressed during cold acclimation differ between the two species.

85 effect usually exceeded the magnitude of the acclimation effect.

86 Our models further project that acclimation effects could potentially halve increases in

87 ually exclusive hypotheses regarding thermal acclimation effects on infection of green frog tadpoles

88 emperature responses and longer-term thermal acclimation effects.

89 Thus, acclimation eliminated 80% of the expected increase in l

90 ndicate that gene expression during sub-zero acclimation follows a tighly controlled time-course.

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

92 During cold acclimation freezing tolerance of the Hv-CBF2A overexpre

93 The data documented an E. coli acclimation gradient where progressively more severe iro

94 Short-term cold acclimation has been shown not only to enhance the prese

95 ate constitutive freezing tolerance and cold acclimation in Arabidopsis.

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

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

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

99 t type (Symbiodinium spp.) facilitated rapid acclimation in Porites divaricata, whereas low energy re

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

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

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

103 Furthermore, cold acclimation increased BAT activity in parallel with incr

104 es all three Mediator subunits, as does cold acclimation-induced freezing tolerance.

105 l of this study was to determine how thermal acclimation influences host resistance to infection and

106 Although cold acclimation is a key process in plants from temperate cl

107 to one another, and to a null model in which acclimation is ignored.

108 in freezing tolerance that occurs with cold acclimation is only partially dependent on the CBF-CRT/D

109 Key to acclimation is the type II NADPH dehydrogenase, NDA2, wh

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

111 Here we describe a mutant, singlet oxygen acclimation knocked-out 1 (sak1), that lacks the acclima

112 UV-B exposure, at low levels that induce acclimation, led to broad changes in the Chlamydomonas t

113 ng (short-term plasticity) and developmental acclimation (long-term plasticity) are positively correl

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

115 However, physiological acclimation may dampen or eliminate this response.

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

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

118 ese changes, they have developed a series of acclimation mechanisms.

119 low water-potential controls many downstream acclimation mechanisms.

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

121 Sequential monthly acclimation modulated BAT reversibly, boosting and suppr

122 esponse of wild-type plants with that of the acclimation mutant stn7, we could specifically identify

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

124 We found that for 48 weeks, before acclimation occurred, an experimental 3 degrees C increa

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

126 irement for COR15 accumulation for full cold acclimation of Arabidopsis.

127 Despite the physiological acclimation of autotrophic respiration to warming, incre

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

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

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

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

132 Acclimation of leaf respiration per degree temperature c

133 Here we demonstrate strong acclimation of leaf respiration to both experimental war

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

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

136 tosolic fumarase FUM2, is essential for cold acclimation of metabolism in the cold-tolerant model spe

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

138 d of growth and compared these results with acclimation of PhiPSII to a step-wise change in irradian

139 We measured the acclimation of PhiPSII to constant growth irradiances of

140 Understanding physiological acclimation of photosynthesis and respiration is importa

141 Thermal acclimation of photosynthesis can be modelled as changes

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

143 1 and Lhcb2 plays contrasting roles in light acclimation of photosynthesis.

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

145 The acclimation of plants to changes in light intensity requ

146 atory mechanism that ensures the appropriate acclimation of plants to daily and seasonal changes in t

147 The acclimation of plants to light has been studied extensiv

148 pts play an important biological role in the acclimation of plants to light stress.

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

150 or the key role of the MPK3-SUB1A1 module in acclimation of rice seedlings to the adverse effects of

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

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

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

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

155 ed-potential incubation, indicating that the acclimation of the biocathode resulted in performance im

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

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

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

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

160 is a model anaerobic methanogen to study the acclimation of water-deficit stresses which de novo synt

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

162 We examined the effects of temperature acclimation on BAT, energy balance, and substrate metabo

163 py LD nullified the effect of leaf hydraulic acclimation on GS .

164 odels, we projected the influence of thermal acclimation on: seasonal variation in R; spatial variati

165 compare the measured effects of respiration acclimation-over-time and variation-across-space to one

166 The measured strength of acclimation-over-time produces differences in annual R a

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

168 europaea chemostat cultures demonstrated an acclimation period that was characterized by transient d

169 a 20-week experiment that included a 4-week acclimation period with a high number of replicate tanks

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

171 old were slightly improved at the end of the acclimation period.

172 n removal (>94%) was observed after a 29-day acclimation period.

173 ated drought stress for 21 d following a 5 d acclimation period.

174 e the observed differences between the light acclimation periods.

175 Photosynthetic acclimation (photoacclimation) is the process whereby le

176 During cold acclimation plants increase in freezing tolerance in res

177 Here we investigate the acclimation potential of stony corals living along a pH

178 pected respiration increase, but the thermal acclimation potential of tropical forests remains largel

179 Chlamydomonas UV-B acclimation preserved the photosystem II core proteins D

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

181 -induced coma and this ongoing physiological acclimation process allowed some individuals of the tole

182 ITION7, and is directly related to the light acclimation process called state transitions.

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

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

185 of Chl f (and Chl d) is part of an extensive acclimation process, far-red light photoacclimation (FaR

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

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

188 Acclimation reduced daily modeled respiratory losses fro

189 Acclimation reduced the degree to which respiration incr

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

191 BF genes themselves are activated after cold acclimation remains poorly understood.

192 This suboptimal acclimation renders a large portion of residual photosyn

193 that increased V-ATPase activity during cold acclimation requires the presence of the V-PPase.

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

195 have been attributed to either cell death or acclimation, respectively.

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

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

198 imation knocked-out 1 (sak1), that lacks the acclimation response to singlet oxygen.

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

200 A much simpler acclimation response, low-light photoacclimation (LoLiP)

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

202 opies wild-type metabolic and transcriptomic acclimation responses after the shift from high to low C

203 family of related receptors known to mediate acclimation responses and to reduce transpiration.

204 re of rapid cold hardening and developmental acclimation responses are nonoverlapping at the SNP and

205 hain that acts as a trigger for compensatory acclimation responses comprising functional and structur

206 The acclimation responses observed here suggest that warmer

207 oductivity, yet the genetic bases of drought acclimation responses remain poorly understood.

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

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

210 ial opportunity for short-term and long-term acclimation responses to evolve separately from each oth

211 However, host acclimation responses varied depending on the stage of i

212 layed a multitiered, hierarchical cascade of acclimation responses with different Fe thresholds.

213 -temperature environments because of thermal acclimation responses, i.e. physiological changes that a

214 stance to infection and to test for parasite acclimation responses, which might differ from host resp

215 photophysiology as Fe declined, yet used few acclimation responses.

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

217 ROS perception and distal systemic acquired acclimation (SAA).

218 to sulfur-limited growth conditions, sulfur acclimation (sac) mutants, which are more severely defec

219 limate warming in the model relative to a no-acclimation scenario, leading to 21% greater increase in

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

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

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

223 both local and long distance RBOH-dependent acclimation signaling that is distinct from other HL sig

224 wered regarding both the regulation of these acclimation states and the molecular mechanism underlyin

225 At least two limiting-CO2 acclimation states, termed low CO2 and very low CO2, hav

226 In this work, we have studied the acclimation strategies of Chlamydomonas reinhardtii, a m

227 wth environments and gives new insights into acclimation strategies to these environmental conditions

228 identify both general and nutrient-specific acclimation strategies.

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

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

231 UTER 1 are required for both HL and systemic acclimation stress perception.

232 between basal cold tolerance and short-term acclimation suggests less constraint.

233 tween basal cold tolerance and developmental acclimation suggests that basal cold tolerance may const

234 While acclimation temperature positively affected the upper cr

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

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

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

238 were independently acclimated to a range of 'acclimation temperatures' prior to shifting them to new

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

240 trace changes in gene expression during cold acclimation that lead to an increase in cold tolerance.

241 and measured at ambient temperature; without acclimation, these increases would have been 23%.

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

243 rming resulted in significant changes across acclimation time.

244 al muscle Mito(VD) may increase with 28 days acclimation to 3454 m.

245 hlighted the importance of systemic acquired acclimation to abiotic stresses in plants and identified

246 natural CO2 vents reveals little evidence of acclimation to acidification or temperature changes, exc

247 , respectively, is an important regulator in acclimation to changing light environments.

248 r state transitions, are not associated with acclimation to changing light intensity.

249 ery, with central roles in light capture and acclimation to changing light.

250 ck of evidence on long-term (weeks to years) acclimation to climate warming in field settings current

251 Does physiological acclimation to climate warming mirror acclimation to sea

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

253 f nine genes potentially involved in Daphnia acclimation to cyanobacteria: six protease genes, one ub

254 in stressful light conditions, allowing for acclimation to different and changing environments.

255 treatments, suggesting that root growth and acclimation to elevated CO(2) were quantitatively more i

256 ter plasticity in Topt , resulting in better acclimation to elevated temperatures.

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

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

259 eparately from each other and for short-term acclimation to evolve separately from basal thermotolera

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

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

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

263 ed growth was contrasted experimentally with acclimation to glucose-limited growth to identify both g

264 Also, acclimation to high (10(-9) M free Co(2+)) or low (10(-1

265 orylation is critical for driving successful acclimation to high light and anoxic growth environments

266 Acclimation to iron-limited growth was contrasted experi

267 The genetic variation for photosynthetic acclimation to irradiance found in this study will allow

268 ort-term temperature change, and respiratory acclimation to long-term warming treatments.

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

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

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

272 Acclimation to nutrient limitation did however involve s

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

274 s for predictions of forest productivity and acclimation to rapid climate change.

275 Acclimation to realistic daily heat pulses enhanced ther

276 ogical acclimation to climate warming mirror acclimation to seasonal temperature changes?

277 genome-wide changes in RNA abundance during acclimation to singlet oxygen revealed that SAK1 is a ke

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

279 e (H2S) and nitric oxide (NO) enhances plant acclimation to stress; however, the underlying mechanism

280 tants, which are more severely defective for acclimation to sulfur limitation, do not have cell cycle

281 ugh we observed that smt15-1 has a defect in acclimation to sulfur-limited growth conditions, sulfur

282 of metabolic modeling to the study of plant acclimation to the environment.

283 The results show that after acclimation to the LM medium, exposure to high free Ca(2

284 hort-term temperature increase but showed no acclimation to the long-term warming.

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

286 The competence for qE induced by acclimation to UV-B markedly contributes to photoprotect

287 Rd acclimation to warmer temperatures caused a reduction in

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

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

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

291 During far-red acclimation, transcript levels increase more than twofol

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

293 Hypoxia acclimation was not associated with changes in gill morp

294 Rd acclimation was similar across plant types.

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

296 Gene expression responses to elevated CO2 (acclimation) were modest [33-131 genes differentially ex

297 l cold tolerance may constrain developmental acclimation, whereas a weaker negative correlation betwe

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

299 glucose uptake tended to increase upon cold acclimation, which was paralleled by increased basal GLU

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