ライフサイエンスコーパス: assimilation

1 gesting their involvement in in situ linuron assimilation.

2 ow response reduces the efficiency of carbon assimilation.

3 econstruction of LGM temperatures using data assimilation.

4 ve regulator of sulphate/selenate uptake and assimilation.

5 pact organisms that require formaldehyde for assimilation.

6 synthesis on carbon-use efficiency and total assimilation.

7 leaf-level processes from plant-level carbon assimilation.

8 d investigate inorganic nitrogen and sulfate assimilation.

9 tems to oxidoreductases involved in nutrient assimilation.

10 ce excess nitrogen (N) from water column via assimilation.

11 ve during both aerobic and anaerobic nitrate assimilation.

12 esponse to optimise N utilisation for carbon assimilation.

13 lifestyle alongside with anaplerotic carbon assimilation.

14 , consistent with limited nighttime nitrogen assimilation.

15 emmerer & Berry (FvCB) representation of CO2 assimilation.

16 itide signaling, gluconeogenesis, and sulfur assimilation.

17 nal variation in eddy covariance-derived CO2 assimilation.

18 trons to a host protein involved in nutrient assimilation.

19 hly half of the global photosynthetic carbon assimilation.

20 newly learned information, allowing cortical assimilation.

21 ose, demonstrating its relevance for pentose assimilation.

22 g induction may cost > 20% of potential crop assimilation.

23 substantial differences in total crop carbon assimilation.

24 her green tissues make to whole-plant carbon assimilation.

25 xylase/oxygenase (Rubisco) to enhance carbon assimilation.

26 imated PSII electron transfer rate and CO(2) assimilation.

27 g their contribution to xylose transport and assimilation.

28 take, regardless of species, was linked to C assimilation.

29 ization hypotheses: water uptake (1), carbon assimilation (2), sucrose transport (3), or (4) profit f

30 xplores coordination between g(s) and carbon assimilation (A) and the influence of spatial distributi

31 K(leaf) ), stomatal conductance (g(s) ), net assimilation (A), vein embolism and abscisic acid (ABA)

32 onthly, annual and decadal rhythms of carbon assimilation (A).

33 er uses three forecasting machines: (i) data assimilation, a technique borrowed from atmospheric phys

34 seven European shrublands using indices of C assimilation (aboveground net primary production: aNPP)

35 Modeling soybean yields based on carbon assimilation alone underestimated yield loss with high-i

36 be selected through a process called genetic assimilation, although the mechanisms are still poorly u

37 The variation of carbon assimilation among cultivars was three times greater und

38 ons in leaf water potential (Psi), net CO(2) assimilation (An) and stomatal conductance (gs) due to w

39 tic relatedness and ecology in determining C assimilation, an essential variable in gas-exchange-base

40 of a novel cellular phenotype by the genetic assimilation and adaptive refinement of a plastic trait

41 of Rubisco that also directly impedes carbon assimilation and allocation.

42 his refines the current paradigm that canopy assimilation and below-ground respiration are tightly co

43 nsport with concomitant reductions in carbon assimilation and biomass production when effects on resp

44 expression of genes involved in nitrogen (N) assimilation and carbon (C) metabolism, which may redire

45 incomplete degradation and multiple-element assimilation and combined it with a dynamic model for fa

46 To improve poplar's capacity for Zn assimilation and compartmentalization, it is necessary t

47 sion of several genes involved in the sulfur assimilation and cysteine biosynthetic pathways.

48 equires rapid and substantial increases in N assimilation and demonstrate that this process is depend

49 s to data; model-data benchmarking; and data assimilation and ecological forecasting.

50 The rates of assimilation and efflux of xylem-transported CO(2) incre

51 nate stomatal behavior with mesophyll carbon assimilation and explore stomatal kinetics as a possible

52 ple autotrophic pathways of microbial carbon assimilation and fixation in paddy soils remain poorly c

53 stinal function, insulin secretion, nutrient assimilation and food intake.

54 crops, potentially improving their nutrient assimilation and growth.

55 ed the response to nitrate, enhanced nitrate assimilation and improved biomass and root development.

56 we obtained a systems-level understanding of assimilation and intracellular distribution of nitrogen.

57 trophic modes, proteins involved in nitrogen assimilation and light-independent chlorophyll synthesis

58 aken together, these findings show that heme assimilation and metabolism in the anaerobe B. fragilis

59 Rubisco in vitro, it is not known how CO(2) assimilation and plant growth are impacted.

60 mportantly, lncRNA T5120 can promote nitrate assimilation and plant growth to improve nitrogen use ef

61 In Malaga, the assimilation and progression of the diagnostic and thera

62 stood, as are the evolutionary mechanisms of assimilation and refinement.

63 es are hypothesized to regulate acquisition, assimilation and remobilization of N and P.

64 candidates for root architecture, N uptake, assimilation and remobilization.

65 trolled by traits related to carbon cycling (assimilation and respiration) in well-watered trees, to

66 ion and central metabolism, including carbon assimilation and respiration.

67 thesis to cytoskeletal dynamics and cofactor assimilation and serve as models for uncovering strategi

68 nd NLP6&7-dependent up-regulation of nitrate assimilation and signaling genes and down-regulation of

69 ses to nitrate availability, linking nitrate assimilation and signaling with cell-cycle progression.

70 piration can be decoupled from recent canopy assimilation and that stored carbohydrates can be mobili

71 olved in water to simultaneously measure the assimilation and the efflux of xylem-transported CO(2) e

72 stigating evolutionary principles of genetic assimilation and the survival mechanisms of natural popu

73 ative metabolism, with a reliance on nitrate assimilation and the urea cycle to help fuel energy prod

74 o regulate several genes involved in sulfate assimilation and to contribute to the growth of V. fisch

75 xylation rate (V(cmax) ), to simulate carbon assimilation and typically rely on empirical estimates,

76 crobial hydrolases, and subsequent microbial assimilation and utilization of the hydrolysis products

77 jointly regulate the tradeoff between carbon assimilation and water loss.

78 These are inhibition of food assimilation and/or decreased nutritional value of food,

79 lecting individual variation in acquisition, assimilation and/or recycling of plasma proteins that pr

80 l similarity in carbon, nitrogen, and sulfur assimilation, and aerobic nitrogen cycling.

81 into and growth within host cells, nutrient assimilation, and alterations in host ion flux.

82 hotosynthesis rates, increased leaf nitrogen assimilation, and enhanced source-to-sink transport of a

83 ic sensitivity tests, enable pool-based data assimilation, and facilitate tracking and benchmarking o

84 TCA cycle, heterotrophic pathways for carbon assimilation, and methylotrophic pathways for energy con

85 ies per community) on plant growth, nutrient assimilation, and soil nutrient dynamics via seed-inocul

86 meter studies varying properties of the data-assimilation approach including the time interval betwee

87 trates the feasibility and utility of a data-assimilation approach to forecasting the fate of cells u

88 In this study, we demonstrate that a data-assimilation approach using an ensemble Kalman filter, w

89 ypical LD acclimation of carbon and nitrogen assimilation as well as redox-related parameters was not

90 r plant (shoot and root) growth and nutrient assimilation as well.

91 up-regulation of sulfate/selenate uptake and assimilation, associated with elevated concentrations of

92 upt decline in quantum yield (QY) of net CO2 assimilation at low photosynthetic photon flux density (

93 ad to a marked (45%) overestimation of CO(2) assimilation at subsaturating irradiance and low tempera

94 ics in between the analysis cycles and/or by assimilation at the next analysis cycle.

95 a Biolog assay determining the carbon source assimilation behavior of an xpp1 deletion strain.

96 d for 39-100% of species-level annual carbon assimilation, but summer and autumn accounted for large

97 rating mechanism that can increase net CO(2) assimilation by capturing, concentrating and re-assimila

98 Nearly all algae enhance their carbon assimilation by operating a CO2-concentrating mechanism

99 Mycorrhizal-acquired nutrient assimilation by plants may be symmetrically linked to ca

100 For example, riverine organic matter assimilation by the glacier-nesting seabirds Kittlitz's

101 Inefficiencies in photosynthetic carbon assimilation can be overcome by synthetic biology strate

102 aulic conductance, stomatal conductance, and assimilation capacities should be positively correlated.

103 Instead of possessing high assimilation capacities to match high specific stem cond

104 iva) subspecies differ in nitrate (NO(3)(-)) assimilation capacity and nitrogen (N) use efficiency (N

105 ponsive aeration with changing environmental assimilation capacity.

106 ranscription factors, transporters, nitrogen assimilation, carbon/nitrogen metabolism, redox, signall

107 NP enhanced tissue ARV assimilation compared to plasma.

108 tially partitioned into niches where nitrate assimilation conferred a fitness benefit.

109 We then highlight data assimilation (DA) as an effective way to reconcile diffe

110 Here, we explore data assimilation (DA) with the Ensemble Kalman filter to fus

111 ver, the per plant growth and plant nutrient assimilation declined, most likely, due to microbial-dri

112 tputs, including hydraulic damage and carbon assimilation diagnostics, moderately improve mortality p

113 pt abundances for genes involved in ammonium assimilation differed from the classical "enteric paradi

114 s, and they maintained a lower rate of CO(2) assimilation during both photoperiod types.

115 primary productivity through enhanced carbon assimilation early in the growing season, which leads to

116 hat concentrates CO2 near RubisCO increasing assimilation efficacy.

117 Zinc assimilation efficiency (AE) varied from 28% for the Ani

118 Photosynthetic carbon assimilation enables energy storage in the living world

119 es encoding high substrate affinity nitrogen assimilation enzymes (GS-GOGAT system) was similar in gr

120 eveloped an integrated compartment model and assimilation filtering forecast model for real-time fore

121 e used to estimate a 14% reduction in carbon assimilation for one day over sagebrush dominated areas

122 We measured the temporal dynamics of carbon assimilation for seven native herbaceous perennials and

123 lationship between leaf structure and carbon assimilation, for defining the relative investments in l

124 The data assimilation forecasts are empirically evaluated against

125 our study on the quantification of deuterium assimilation from heavy water into single bacterial cell

126 cently been proposed to function in nitrogen assimilation from l-Arg.

127 al by NaPAA hydrogels followed by biological assimilation from the growth of ordinary heterotrophic o

128 Nitrate assimilation genes are absent in basal lineages but occu

129 rtitioning set the stage for loss of nitrate assimilation genes from basal lineages as they specializ

130 The distribution of nitrate assimilation genes within clades appears largely governe

131 ess the impact of these delays on net carbon assimilation have used simplified models of crop canopie

132 for accurately modelling net rates of CO(2) assimilation, (ii) on how leaf biochemical and anatomica

133 stimation of the capacity for leaf-level CO2 assimilation in Arctic vegetation.

134 2.5% of the total assimilation in both species in the highest [(13) CO(2)

135 the existence of an SBP pathway for pentose assimilation in cellulolytic clostridia.

136 ganelle that plays essential roles in carbon assimilation in cyanobacteria and chemoautotrophs.

137 neering of the cell biology supporting CO(2) assimilation in diverse organisms.

138 Ammonium assimilation in Escherichia coli is regulated by two par

139 degraded cytoplasm and an absence of (13) C assimilation in foraminifera exposed to light.

140 lanine dehydrogenase is involved in ammonium assimilation in M. tuberculosis, in addition to its esse

141 to the requirement of mft genes for ethanol assimilation in Mycobacterium smegmatis mc(2)155.

142 , we investigate possible inorganic-compound assimilation in Nonionellina labradorica, a common klept

143 ent availability needed for plant carbon (C) assimilation in response to CO(2) enrichment (eCO(2) ).

144 VdAtf1 affects ammonium and nitrate assimilation in response to various nitrogen sources.

145 ive nitrogen in generalists but for nitrogen assimilation in specialists.

146 ts suggest that PPSB is required for sulfide assimilation in specific heterotrophic tissues and that

147 reaction represents the first step in carbon assimilation in the acetogenic and methanogenic branches

148 g the importance of lipid transport and iron assimilation in the progression of the disease.

149 explore the metabolic networks for nitrogen assimilation in this bacterium, changes in gene expressi

150 follow nicotine biotransformation and lipid assimilation in vivo to demonstrate the concept.

151 ed in each zone by using cyanide to block Pi assimilation in wild-type plants and a vacuolar Pi trans

152 ctivity of key enzymes involved in primary N assimilation, including nitrate reductase (NR) and alani

153 n of Flavobacteria and Rhodobacteraceae to C assimilation increased up to sixfold and twofold, respec

154 ons and large duplications, suggesting tight assimilation into host genomes.

155 fects of both harsh migration conditions and assimilation into host population conditions.

156 alysis and/or detergent absorbents, and A2AR assimilation into synthetic liposomes can be visualized

157 the 7th century and in agreement with their assimilation into the Indian sub-continent's population

158 les was inferred from calculations of (66)Zn assimilation into the snail's soft tissues.

159 to complex carbon substrates, the deuterium assimilation is higher in the presence of simpler substr

160 The first step in exogenous fatty acid assimilation is phosphorylation by fatty acid kinase (Fa

161 alistic light regimes a 100% boost to carbon assimilation is possible.

162 lism compared to predation or organic matter assimilation is unknown.

163 mine synthetase, the key enzyme for nitrogen assimilation, is poorly understood.

164 ariation in type and number of transporters, assimilation machinery, and anatomical features that can

165 Data assimilation makes it possible to rigorously estimate pa

166 ate all known autotrophic pathways and CO(2) assimilation mechanisms in five typical paddy soils from

167 d the abundance of Calvin Cycle and nitrogen assimilation metabolites while suppressing the abundance

168 ion dynamics, which we optimize using a data assimilation method and two observed data streams, mosqu

169 ) model and an ensemble Kalman filter (EnKF) assimilation method, we developed an integrated compartm

170 Assimilation methods, meant to constrain divergence of m

171 observations of influenza incidence and data assimilation methods.

172 ions with climate reanalysis data, snow data assimilation model output, and satellite spectral data.

173 the emerging application of in silico carbon assimilation models.

174 ts are associated with elevated plant carbon assimilation, nitrogen utilization, and plant growth.

175 Because sulfate assimilation occurs mainly in the light, we also investi

176 nt into the chloroplast, where primary CO(2) assimilation occurs.

177 The COVID-19 pandemic demands assimilation of all biomedical knowledge to decode mecha

178 ole-rock or zircon isotope studies, and that assimilation of altered roof material may represent a vi

179 methane monooxygenase, the serine cycle for assimilation of carbon from CH(4) and CO(2), and CO(2) f

180 ynthesis, with primary production based upon assimilation of CH(4) and CO(2) by methane- and hydrogen

181 me marine forecasting system, along with the assimilation of climatological monthly mean Argo data to

182 three key questions: Q1 Does light-dependent assimilation of CO(2) via RuBisCo dictate the rate of ma

183 Our results show partial re-assimilation of CO2 and H2 by n-butanol-producer C. beij

184 ultural explanations such as exposure to and assimilation of culturally transmitted ideologies.

185 YtnA), which we show has a major role in the assimilation of D-alanine from the environment.

186 s with parameters estimated from large-scale assimilation of electrophysiological recordings, we succ

187 encodes a cell-surface protein required for assimilation of exogenous heme.

188 In contrast, long-term assimilation of Fe by live cells yielded preferential in

189 ough the feeding activity of the animals and assimilation of filtered particles in shellfish tissues.

190 e climatological monthly mean Argo data, the assimilation of glider-observed T/S profiles is efficien

191 the dispersal process and the replacement or assimilation of indigenous human populations such as the

192 The assimilation of inorganic compounds in foraminiferal met

193 The assimilation of magnetic nanoparticle synthesis into mam

194 ent work showed that the bioavailability and assimilation of meat amino acids in the elderly is lower

195 ese shocks are essentially eliminated by the assimilation of near-homogenous global Argo distribution

196 large B cell lymphoma (DLBCL) requires rapid assimilation of new biological data.

197 f the famous face after learning, suggesting assimilation of new into old memories.

198 Assimilation of novel strategies into a consolidated act

199 efficiency higher than 100%, suggesting the assimilation of other carbon, very likely CO(2), into th

200 ation sources into disease surveillance, the assimilation of such data into models of pathogen spread

201 terotrophic values associated to mixotrophic assimilation of synthesis gas (H2, CO2 and CO).

202 uction of the basin-wide model biases by the assimilation of the climatological monthly mean Argo dat

203 In this study, we investigated the DIC assimilation of the green alga Dunaliella tertiolecta af

204 We demonstrated that a sequential assimilation of the green fraction derived from Red-Gree

205 of zero in more-alkaline fluids and prevent assimilation of the individual framboids into a single g

206 This eventually leads to genetic assimilation of the silent phenotype by mutations that r

207 l modification, ring opening, and subsequent assimilation of these compounds into the tricarboxylic a

208 climate resilience and efficiency of carbon assimilation of this cereal crop as temperatures become

209 (2) exiting the leaf in the dark or rates of assimilation of xylem-transported CO(2) * in the light,

210 Assimilation of xylem-transported CO(2) comprises a smal

211 thousand, due to magma residence within, and assimilation of, local granite basement.

212 ons result in a 13% reduction in crop carbon assimilation on both sunny and cloudy days, with inducti

213 These results indicate that life-history and assimilation outcomes depend on key differences between

214 cose forecasts; (ii) model averaging of data assimilation output; and (iii) dynamical Gaussian proces

215 importance of these delays on net cumulative assimilation over the course of both a sunny and a cloud

216 Passing Attributes between Networks for Data Assimilations (PANDA) to construct the gene regulatory n

217 Pathogens rely on nutrient assimilation, particularly essential metal incorporation

218 The altered carbon assimilation pathway of crassulacean acid metabolism (CA

219 ation of C3 photosynthesis (the basic carbon-assimilation pathway present in all plants) is alleviate

220 Fe-containing enzymes of the plastid sulfur assimilation pathway were major targets of Fe deficiency

221 ifera might have several ammonium or sulfate assimilation pathways, involving either the kleptoplasts

222 ecies showed significant variation in carbon assimilation patterns.

223 minutum exhibited high photosynthetic carbon assimilation per cell and translocation to host tissue t

224 ctivity and any gain in photosynthetic CO(2) assimilation per unit of leaf area (A) has the potential

225 artially restored the nitrate signalling and assimilation phenotypes of nlp7 mutant, suggesting that

226 te feeding resulted in the inhibition of net assimilation, photosynthetic electron transport, and iso

227 N response of genes involved in N uptake and assimilation (primary metabolism) as well as stress resp

228 ed that PPSB deficiency perturbs the sulfate assimilation process between tissues/organs.

229 filling wheat plants face limitations to the assimilation process due to natural senesce and water st

230 tant, suggested interaction with the sulfate assimilation process.

231 Specifically, chlorine assimilation provides key evidence of recycling in subma

232 Escherichia coli strain deficient in sulfite assimilation, pssm2-Fd complemented bacterial growth whe

233 s(-1) increase in the maximum photosynthetic assimilation rate (A(max)), with croplands having strong

234 conductance to water vapour g(s) ) and CO(2) assimilation rate (A) applies to all major lineages of v

235 p between mass-based stem photosynthetic CO2 assimilation rate (Amass ) and specific stem area (SSA;

236 Here, we show that growth rate and carbon assimilation rate of soil microorganisms are influenced

237 trinsic water use efficiency (WUE(i) ; CO(2) assimilation rate per stomatal conductance).

238 f area index (LAI) and increasing leaf-level assimilation rate related to leaf demography), and alloc

239 tic parameters were derived from analysis of assimilation rate vs internal CO2 concentration curves (

240 ion (~50% to ~90%) in growth rate and carbon assimilation rate was attributable to differences among

241 eaf temperature, lower photosynthetic carbon assimilation rate, and growth inhibition.

242 the ongoing endeavors to enhance crop CO(2) assimilation rate, growth, and yield.

243 Overall, these results indicated that carbon assimilation rate, the K battery, root starch synthesis,

244 dation in deeper anoxic horizons have a high assimilation rate, whereas cells performing oxygen reduc

245 solar exposure are important predictors of C assimilation rate.

246 nlinear relationship between light and CO(2) assimilation rate.

247 e role of each family in relation to the net assimilation rate.

248 ght, where provenances sustaining higher CO2 assimilation rates also revealed increased water-use eff

249 multiple temperatures, focusing on net CO(2) assimilation rates and leaf dark respiration rates measu

250 nhanced stomatal conductance, photosynthetic assimilation rates and, to a lesser extent, tree radial

251 range of chlorophyll contents and net CO(2) assimilation rates can be achieved in maize by combining

252 CO(2) reconstructions that apply C assimilation rates from modern species based solely on p

253 to quantify ammonium and nitrate uptake and assimilation rates in four 40-yr-old monoculture conifer

254 rations and reduced stomatal conductance and assimilation rates in our eight sample species.

255 e text] that was directly linked to elevated assimilation rates of [Formula: see text] (A).

256 e-based CO(2) reconstructions use carbon (C) assimilation rates of extant plant species as substitute

257 s of extant plant species as substitutes for assimilation rates of fossil plants.

258 structions should be determined by averaging assimilation rates of modern plant species that are (1)

259 C assimilation rates used in CO(2) reconstructions should

260 Taxon-specific growth and carbon assimilation rates were highly intercorrelated across th

261 tial reduction in both respiration and CO(2) assimilation rates.

262 d smaller and had lower photosynthetic CO(2) assimilation rates.

263 efficiency (WUE(i) , the rate of leaf CO(2) assimilation relative to water loss via stomatal conduct

264 regulation of ammonium transport and nitrate assimilation, restriction of protein degradation by auto

265 Carbon (C) assimilation, Rubisco activity, CA1Pase activity, transc

266 r conditions (sink limitation), while carbon assimilation (source limitation) plays a secondary role.

267 sphorylation that senses carbon and nitrogen assimilation status.

268 sion of iron-sulfur cluster (ISC) and sulfur assimilation (SUF) systems for iron-sulfur cluster biosy

269 me encodes two heme uptake systems, the heme assimilation system (Has) and the Pseudomonas heme utili

270 Extracellular heme is sensed via a heme assimilation system (has) that encodes an extracytoplasm

271 int) SM/ST dataset prepared from a land data assimilation system, as part of a national monsoon missi

272 nsporters but found no evidence of a nitrate assimilation system, in agreement with the N preference

273 ological variables from the Global Land Data Assimilation System: daily total precipitation volume (m

274 servations in two different ocean models and assimilation systems, that such shocks are generated in

275 monstrate that our Bayesian-based data-model assimilation technique is able to discover onchocerciasi

276 ransmission models using Bayesian data-model assimilation techniques to baseline and follow-up infect

277 ghtly higher stomatal conductance and carbon assimilation than wild-type plants; however, these param

278 Finally, genes involved in sulfur assimilation, the glutathione-ascorbate cycle, and vario

279 the disequilibrium state via long-term data assimilation, thereby effectively reducing the uncertain

280 metabolite isotopologues revealed nonuniform assimilation throughout the metabolic network.

281 red the temperature of photosynthetic carbon assimilation to be a constant value of c. 20 degrees C;

282 ter-use efficiency (WUE)-the ratio of carbon assimilation to water loss-has increased in recent decad

283 Nitrogen acquisition and assimilation transcripts become elevated in symbiotic Br

284 eawater flooding significantly reduced CO(2) assimilation, transpiration and stomatal conductance, bu

285 mproved understanding of the regulation of C assimilation under heat stress will inform efforts to im

286 Under saturating irradiance, rates of assimilation using xylem-transported CO(2) accounted for

287 atistically rigorous approach, that is, data assimilation, vary with time, space, and treatments in g

288 plement channel resistance by limiting toxin assimilation via the digestive process.

289 Phaeodactylum tricornutum In NR-KO cells, N-assimilation was abolished although NO3(-) transport rem

290 Daily C assimilation was greater at elevated [CO2 ] in both cult

291 cellular and genetic basis of diatom NO3(-) assimilation, we generated a knockout in the nitrate red

292 degrees C warming conditions, and calculated assimilation-weighted leaf temperature (T(L-AW) ) across

293 and AQP for N uptake and GOGAT and GS for N assimilation were the key genes, validated by RT-qPCR, w

294 ect on the processes most limiting to carbon assimilation, which differ by plant type.

295 synthesis also displayed higher rates of ear assimilation, which translated to increased grain yield.

296 Plants optimize carbon assimilation while limiting water loss by adjusting stom

297 er use models predict leaves maximize carbon assimilation while minimizing water loss via transpirati

298 still provides a substantial boost to carbon assimilation with only a moderate decrease in efficiency

299 These quantities link carbon (C) assimilation with transpiration, and along with photosyn

300 Nutrient assimilation within plant tissues did not correlate with