ライフサイエンスコーパス: respiration rate

1 threshold for ecosystem function (i.e. soil respiration rate).

2 en formal mindfulness practice and decreased respiration rate.

3 ctivity, but rather by greater reductions in respiration rate.

4 consistently showed a reduced ADP-stimulated respiration rate.

5 starch, and glutathione levels and a reduced respiration rate.

6 um feeding was accompanied by a reduction in respiration rate.

7 sponsive down to 0.01x the culture's maximum respiration rate.

8 d ICP response to changes in head-of-bed and respiration rate.

9 d pressure but did not change heart rate and respiration rate.

10 ng blood pressure, increasing heart rate and respiration rate.

11 fibroblasts exhibited an exceptionally high respiration rate.

12 ion as being responsible for the decrease in respiration rate.

13 e for Bcl-2 does not prevent the decrease in respiration rate.

14 th thermodynamic and kinetic controls on the respiration rate.

15 tween its resource assimilation rate and its respiration rate.

16 ange in membrane potential despite increased respiration rate.

17 t to that required to support the endogenous respiration rate.

18 n to clinical bedside observation of WoB and respiration rate.

19 r than BAM15 that results in a lower maximal respiration rate.

20 air, lower leaf temperature, and lower leaf respiration rate.

21 associated metabolic demands by altering its respiration rate.

22 ted with composition, despite convergence in respiration rates.

23 tect ferrocyanide or which affected cellular respiration rates.

24 ey functional enzymes could be used to infer respiration rates.

25 s, or that physiological acclimation reduces respiration rates.

26 MP stimulation with high UCP1 expression and respiration rates.

27 soil temperatures and potentially lower soil respiration rates.

28 a were used to quantify substrate uptake and respiration rates.

29 ly was due to an increase (27%) in leaf dark-respiration rates.

30 with a concomitant decrease in mitochondrial respiration rates.

31 ng Pelagibacter and SAR86) had extremely low respiration rates.

32 ause temperature controls photosynthesis and respiration rates.

33 ly associated with SOC content and microbial respiration rates.

34 easing rainfall and associated enhanced soil respiration rates.

35 ation occurred without a concomitant rise in respiration rates.

36 additive and comparable effects on microbial respiration rates.

37 potassium levels, and reduced mitochondrial respiration rates.

38 Sorbitol-Ca reduced respiration rates (15.63 vs. 21.57 mg CO2 kg(-1) h(-1))

39 that the 3460A mutation reduced the maximal respiration rate 20-28%, the 11778A mutation 30-36%, and

40 -75%), basal area increment (-39%), and bole respiration rates (-28%).

41 17 times that of forest soil-based MFCs and respiration rates about 10 times higher than forest soil

42 mRNA target levels plateaued or declined at respiration rates above 5 mueeq/L-hr.

43 -causing nonlinear shifts in total community respiration rates across temperatures via coordinated ch

44 There is an expectation that soil microbial respiration rates adapt to the ambient thermal regime, b

45 ming and magnitude of seasonal heterotrophic respiration rates, again reflecting structural uncertain

46 ion, and a nearly 44% increase in subsurface respiration rates along the coast in summer, reshaping t

47 toheterotrophic conditions and exhibited low respiration rate, although the mutant grew normally unde

48 O exhibited a 42 +/- 19% reduction in tissue respiration rate and a 33 +/- 38% reduction in CcO activ

49 V3 or PIV3 and adenovirus, with an increased respiration rate and body temperature late in the course

50 ch defined by differing parameter values for respiration rate and crop palatability.

51 drial [NADH] ([NADH]m) may regulate cellular respiration rate and energetic state, it is not clear ho

52 . tuberculosis arrests growth, decreases its respiration rate and is resistant to isoniazid, rifampic

53 nstrate continuous detection of temperature, respiration rate and low concentrations of uric acid and

54 CA storage decreased ethylene biosynthesis, respiration rate and membrane permeability.

55 esults from firmness, membrane permeability, respiration rate and microstructural imaging showed that

56 in particular upregulated the mitochondrial respiration rate and mitochondrial volume in winter.

57 arge diameter and high specific root length, respiration rate and nitrogen concentration was driven b

58 fruit had lower weight and firmness losses, respiration rate and production of ethylene than control

59 native gel assay), decrease in mitochondrial respiration rate and reduction of mitochondrial membrane

60 and higher firmness, suppressed browning and respiration rate and sustained soluble solids content, t

61 Notably, the ratio between the dark respiration rate and the maximum carboxylation rate was

62 ng the brain, and is tightly correlated with respiration rate and the phase of respiration cycle.

63 elf life at room conditions by reducing cell respiration rate and water evaporation.

64 hypothermic (30 degreesC) reperfusion, both respiration rates and all enzyme activities remained at

65 Respiration rates and cell concentrations in subseafloor

66 2 millimoles O2 per liter had higher state 3 respiration rates and decreased percentages of alternati

67 der to regulate photosynthetic gas exchange, respiration rates and defend against pathogen entry.

68 e the redox properties of solid phases limit respiration rates and hence organic matter degradation.

69 everal temperate reptiles due to their lower respiration rates and internal temperatures.

70 ADP/ATP recycling mechanism to maintain high respiration rates and low electron leak.

71 The measurement of low respiration rates and low ethylene production during gro

72 nts and simultaneously experienced increased respiration rates and negative carbon budgets due to a 2

73 tion in human cells, resulting in changes in respiration rates and oxidative phosphorylation.

74 Complex I respiration rates and protein levels were 33% lower in h

75 se lines were characterized by no changes in respiration rates and TCA cycle flux, which together wit

76 Because of the low respiration rates and the thinness of the sediment, inte

77 ies revealed differential changes in overall respiration rates and tricarboxylic acid (TCA) cycle flu

78 d allow realistic estimates of cell-specific respiration rates and turnover times for living bacteria

79 hlorophyll content, photosynthetic activity, respiration rate, and antioxidant capacity.

80 in secretion, mitochondrial DNA copy number, respiration rate, and ATP production.

81 amate and alpha-ketoglutarate, mitochondrial respiration rate, and GSH levels and decreases reactive

82 Further, CjEO-CSNP prevented weight loss and respiration rate, and improved the antioxidant activity

83 ity, pupil diameter, electrodermal activity, respiration rate, and phase) or alpha power was observed

84 d increased (P <= 0.01) vaginal temperature, respiration rate, and skin temperatures, but salivary co

85 capacity relative to the residual endogenous respiration rate, and, correspondingly, a higher COX inh

86 stimulation-induced raise in glycolytic and respiration rates, and causes a dramatic defect in ERK a

87 ting community composition, enzyme activity, respiration rates, and residual organic matter reactivit

88 rameters (weight loss, firmness, and color), respiration rate, antioxidant activity and phenolics (me

89 ydrostatic pressure on lethal and sublethal (respiration rate, antioxidant enzyme activity) toxicity

90 to stably express full-length ATM, exhibited respiration rates approaching those of wild-type cells.

91 -regulation of glutamate oxidation supported respiration rates approximating those with pyruvate and

92 HSPC respiration rates are as low as in purified human stem c

93 timulation of lymphocytes, with steady-state respiration rate as a convenient marker of metabolic sti

94 This study identified the (14)C-glucose respiration rate as the best metric to evaluate the effe

95 These results reject respiration rate as the sole factor impacting the tempo

96 nt concentrations, microbial abundances, and respiration rates as well as sequencing bacterial and ar

97 e delay, by a decrease in overall endogenous respiration rate, as measured in vivo in the whole cell

98 Ca content was accompanied by reductions in respiration rate, ascorbic acid degradation, and membran

99 We measured respiration rates associated with leaf litter, wood, and

100 will decrease owing to higher soil and plant respiration rates associated with warming temperatures.

101 ly considered the main driver of daily plant respiration rates, assuming a constant daily respiration

102 ms showed a delay in ethylene production and respiration rate at 20 degrees C and during cold storage

103 respiration rates, assuming a constant daily respiration rate at a set temperature.

104 -acclimated individuals had lower growth and respiration rates at intermediate temperatures than cold

105 e characteristics are known to regulate soil respiration rates at plot scales within certain biomes,

106 Estimated soil respiration rates at the mean microbial biomass were low

107 est how mean annual temperature affects soil respiration rates at three assay temperatures while cont

108 ed, and stems from the fact that relative to respiration rates, bacterial population growth rates typ

109 colysis when excess glucose is available and respiration rate becomes limited by proteome occupancy.

110 Increased respiration rates below WWTPs potentially generate ecosy

111 ied atmosphere, as showed by the increase in respiration rate, biosynthesis of fermentative volatile

112 signs, such as body temperature, heart rate, respiration rate, blood pressure, pulse oxygenation, and

113 FeCl(2) addition initially increased respiration rates, but not the total amount of hydrocarb

114 es in HS pigs increased by 1.6 degrees C and respiration rates by 2-fold (P<0.05).

115 rhizal roots and hyphae decrease soil carbon respiration rates by up to 67% under field conditions in

116 reflected by increased hepatic mitochondrial respiration rates, changes in hepatic gene expression, a

117 xpression of Delta13RAP2.12 led to decreased respiration rates, changes in the levels of tricarboxyli

118 le sugars, sucrose, and vitamin C, but lower respiration rate, chromaticity a(*) and b(*) values, and

119 t cardio-respiratory entrainment at elevated respiration rates, close to the resting heart rate.

120 content and higher ethylene biosynthesis and respiration rate compared to control fruits, showing the

121 Respiration rates, complex I protein and activity, prote

122 At higher temperatures, respiration rates continue to rise in contrast to sharpl

123 uavas coated with P2BO10 exhibited a reduced respiration rate, contributing to better retention of nu

124 Microbial biomass carbon and soil respiration rates decreased significantly across all cyp

125 ces of variability for in vivo data included respiration rate, degree of user experience, and animal

126 phosphorylations are lost leading to maximal respiration rates, DeltaPsi(m) hyperpolarization, ROS pr

127 microbial cells, we show that cell-specific respiration rates differ by more than 1,000x among proka

128 proportion of time resting decreased by 30%, respiration rate doubled and swim speed increased by 37%

129 Soil respiration rates dropped 77%, at 1000 mg kg(-1), and In

130 inkage or indirectly by decreasing microbial respiration rates due to lower redox levels in the soil.

131 imals often exhibited long periods of steady respiration rate during either immobility or running, wh

132 hlight the potential importance of measuring respiration rates during both day and night to account f

133 exercise-real-time recordings of heart rate, respiration rate, energy intensity and other essential v

134 Here we present field measurements, respiration rate estimates and a steady-state model that

135 Respiration rates, ETC protein levels, mitochondrial den

136 t 5 mumol L(-1) was most effective, reducing respiration rate, ethylene evolution, weight loss, and s

137 ring storage, visual quality, physiological (respiration rate, ethylene production, ammonium content)

138 tial, mitochondrial fragmentation, increased respiration rates, exacerbated PINK1/Parkin-dependent mi

139 obustness and accuracy of the heart rate and respiration rate extraction over existing methods.

140 ng of the Baltic Sea will enhance planktonic respiration rates faster than it will for planktonic pri

141 an with ICp in reducing ethylene production, respiration rate, firmness loss, TA increase, and pH dec

142 We measured denitrification and O(2) respiration rates for 10 benthic foraminifer species sam

143 Respiration rates for copepod nauplii increased in the 1

144 Here, we measure microbial respiration rates for soils collected from 22 sites in e

145 The decoupling of respiration rates from abundance among lineages, elevate

146 ireless monitoring of essential vital signs (respiration rate, heart rate and corresponding variabili

147 blood-oxygen saturation, respiratory effort, respiration rate, heart rate, cardiac pre-ejection perio

148 duced, which reduced ethylene production and respiration rate; however, it did not increase physiolog

149 temperature during cold challenges, enhanced respiration rates, improved glucose homeostasis, and red

150 chondrial structure, number, and the maximal respiration rate in Acsl1(T-/-) hearts, but did not impr

151 n by increasing glycolysis and mitochondrial respiration rate in C2C12 muscle cells.

152 RNA and protein biomarkers with chloroethene respiration rate in Dehalococcoides.

153 e causes an early decrease in the endogenous respiration rate in intact 143B.TK(-) cells.

154 The cys-c1 mutation produces a reduction in respiration rate in leaves, an accumulation of reactive

155 erved an increase of maximum coupled state 3 respiration rate in mitochondria isolated from the place

156 nsistent with the previously reported higher respiration rate in mmdh1mmdh2 leaves.

157 CO2 ), and increased precipitation - on soil respiration rates in an annual-dominated Mediterranean g

158 re responsible for significantly higher soil respiration rates in burned sites.

159 States 3, 4, and 5 respiration rates in extraocular muscle mitochondria wer

160 This led to declined respiration rates in fibroblasts and neurons, reduced ce

161 rmocline that have multiplicative effects on respiration rates in low-O(2) water.

162 on isotopes, 'omics' analyses and surveys of respiration rates in mesocosms or ecosystems.

163 neous specific substrate uptake, growth, and respiration rates in response to a continuous-to-batch s

164 e to retain function and even increase basal respiration rates in response to this stress.

165 he measured mass-specific soil heterotrophic respiration rates in soils distributed globally.

166 nderscoring the requirement to maintain high respiration rates in the heart.

167 f intermittent contractions on mitochondrial respiration rates in the human diaphragm following surge

168 Numerous studies have demonstrated that soil respiration rates increase under experimental warming, a

169 Respiration rate increased during the stressful part of

170 pressure, and rate of pressure increase) and respiration rate increased during the stressful part of

171 Respiration rates increased under nutrient-enriched cond

172 Microbial biomass-specific respiration rates increased with incubation temperature,

173 Over the study period, base respiration rates increased with leaf productivity, but

174 Detrital mass-specific respiration rates increased with temperature, exhibiting

175 Dark respiration rates increased, and there were major altera

176 In freely moving mice, instantaneous respiration rate is extremely variable, and respiration

177 Respiration rate is known to correlate with aspects of p

178 rature, Topt ), the temperature at which the respiration rate is most sensitive to changes in tempera

179 iratory synchronization at both low and high respiration rates is associated with a common underlying

180 rest, and their use of energy, inferred from respiration rates, is ~half than that of adults on their

181 This caused increased respiration rates, leading to the observed higher levels

182 nt exposure caused an immediate reduction in respiration rate, likely due to reduced pumping to preve

183 unstable clones, which along with decreased respiration rates may explain the increased levels of ce

184 CA-RQ 1.3) showed lower ethylene production, respiration rate, mealiness and higher flesh firmness in

185 n net CO(2) assimilation rates and leaf dark respiration rates measured at the growth temperature (A(

186 Respiration rate measurements provide an important reado

187 In addition, respiration rate measurements were determined to assess

188 controls) and with (n = 14; breath controls) respiration rate modulation and in adept meditators (n =

189 leaf metabolism and associated with growth (respiration rate, nitrogen and phosphorus concentrations

190 ing this time, we detected no acclimation of respiration rates, no thermal compensation or change in

191 n increasing, unchanging, or even decreasing respiration rates observed in soils.

192 e) oxidase activity, ethylene production and respiration rate of apples stored for 9months at 1.0 deg

193 OA-treatment reduced the respiration rate of artichokes and led to higher total h

194 The respiration rate of mmdh1mmdh2 seeds was significantly e

195 coating could reduce ethylene production and respiration rate of the banana fruit.

196 The respiration rate of whole enod93 seedlings was elevated,

197 The respiration rates of bow-riding dolphins remained relati

198 ion-selective electrode (Ag(+)-ISE) and the respiration rates of E. coli cells were measured by oxyg

199 The respiration rates of free-swimming dolphins increased ex

200 The authors measured respiration rates of isolated mitochondria using a Clark

201 omposition of soil microbial biomass and the respiration rates of leaves and whole crowns.

202 ved a small but significant reduction in the respiration rates of mitochondria.

203 us to calculate realistic, species-specific respiration rates of root branches.

204 a ecosystems are leading to higher microbial respiration rates of soil organic matter, resulting in t

205 acclimation occur generally, the increase in respiration rates of terrestrial plants in response to c

206 ces, also associated with an increase of the respiration rates of the monkey.

207 The per-cell respiration rates of this community are about 2 orders o

208 Climate warming is expected to increase respiration rates of tropical forest trees and lianas, w

209 son's r of 0.89 and 0.88, respectively) with respiration rates on log-log plots between 1.5 and 280 m

210 area, lifespan, photosynthetic capacity and respiration rate) operating along the leaf economic spec

211 ylate (ACC) content along with impediment of respiration rate over 90 days of storage at 25 +/- 2 deg

212 utritional qualities along with reduction in respiration rate (p < 0.05) and preservation of antioxid

213 terial oxygen saturation, end-tidal CO2, and respiration rate (P>0.05).

214 and thawed permafrost endmember OC sources, respiration rates per unit dissolved OC were 1.3-1.6 tim

215 Respiration rates per unit microbial biomass were as muc

216 Even with reduced Q(10), if observed soil respiration rates persist in a warmer world, the feedbac

217 State III mitochondrial respiration rates (pmol O2/s/mg wet weight) were 15.05 +

218 cted than required to support the endogenous respiration rate, pointing to a tighter in vivo control

219 ned high sedimentation caused an increase in respiration rate, potentially due to the energetic cost

220 The decrease in the endogenous respiration rate precedes the release of cytochrome c fr

221 sehip oil (RO) at 2% on ethylene production, respiration rate, quality parameters, bioactive compound

222 rcA, R = 0.91 for MvrD; n = 7) or calculated respiration rate (R = 0.81 for FrcA, R = 0.62 for MvrD;

223 al H2 uptake was correlated with rhizosphere respiration rates (r = 0.8, P < 0.001), and H2 metabolis

224 Corresponding net respiration rates (R) are obtained from a net organic ca

225 Reich et al. report that the whole-plant respiration rate, R, in seedlings scales linearly with p

226 se was mainly due to a decreased autotrophic respiration rate (Ra).

227 Intriguingly, however, day respiration rates remained unaffected.

228 plots, representing some of the highest soil respiration rates reported for any terrestrial ecosystem

229 onverted into oxygen units, the computed net respiration rate represents less than half the oxygen ut

230 rial function, with markedly reduced maximum respiration rate, reserve respiration capacity, and mito

231 Respiration rates responded weakly to gradients in N or

232 with 5.2 % impurities led to an increased in respiration rates, resulting in a CO(2) concentration of

233 The analysis of endogenous respiration rate revealed a significant decrease in the

234 rease in mitochondrial protein synthesis and respiration rates, revealed, in comparison, a significan

235 Restricted changes were recorded in respiration rate, ripening index, and instrumental colou

236 revealed 2-fold variation in nighttime leaf respiration rate (RN) among mature leaves from an Arabid

237 assess underlying ischemia, and estimate the respiration rate (RR) and tidal volume (TV) from analysi

238 On average, LTMs showed slower baseline respiration rate (RR) than Controls.

239 art Rate (HR), Heart Rate Variability (HRV), Respiration Rate (RR), and Blood Pressure (BP) estimatio

240 )Penicillium verrucosum population, (b)CO(2) respiration rates (RR), and (c)ochratoxins concentration

241 respiration rate [RR], colour and moisture loss) and bio

242 ned the effects of fire severity on the soil respiration rate (Rs) and its component change in a Dahu

243 d four experiments, we show that whole-plant respiration rate scales approximately isometrically (sca

244 Annual ecosystem respiration rates show a markedly reduced temperature de

245 Denitrification and O(2) respiration rates significantly scale sublinearly with t

246 Maternal vaginal temperature, respiration rate, skin temperatures, and salivary cortis

247 prominent during immobility and running with respiration rates slower than theta oscillations.

248 In its absence, respiration rate slows and the lack of this electron sin

249 response to increased irradiance, low tissue respiration rate, small amounts of stem and root tissue

250 ved effects of TCS on bacterial abundance or respiration rates, suggesting that bacterial density and

251 Shrub vegetation had the highest respiration rates, suggesting that despite higher rates

252 existing clinical standards for heart rate, respiration rate, temperature and blood oxygenation, but

253 AL displayed a higher baseline mitochondrial respiration rate than SAL.

254 Higher increases in respiration rates than in production may lead to the dep

255 nic substrates is a more dominant control of respiration rates than low temperature.

256 rom KLF4-deficient hearts revealed a reduced respiration rate that is likely due to defects in electr

257 ificantly more than brown ones; both possess respiration rates that are greater than those of higher

258 he dominant hydrocarbon controlling the bulk respiration rates, that the rates peaked around 11 July,

259 ratory acclimation of foliar and whole-crown respiration rates; the trees adjusted to experimental wa

260 intensity fire increased growing-season soil respiration rates through a combination of three mechani

261 in why long-term warming amplifies ecosystem respiration rates through time in recent mesocosm experi

262 at the cause of the high sensitivity of soil respiration rate to changes in snow depth is a unique so

263 re was an initial delay in the return of the respiration rate to normal.

264 al scaling, isometric scaling of whole-plant respiration rate to total nitrogen content is observed w

265 (2) This membrane property coupled with high respiration rates to decrease intracellular O(2) concent

266 ha lipoic acid (ALA), restored mitochondrial respiration rates to levels approaching those of wild-ty

267 on the short-term physiological response of respiration rates to temperature, implying a top-down re

268 ntravenous infusion of Ngb-H64Q-CCC restored respiration rates to that of control mice correlating wi

269 ation to warming, but we observed lower leaf respiration rates under constant water inputs compared t

270 Oxygen measurements showed higher respiration rates under light than dark conditions, and

271 clude that the immediate initial increase in respiration rate upon elevation of work is not activated

272 t there are limits to our ability to predict respiration rates using environmental drivers at the glo

273 ., fungal) drivers of detrital mass-specific respiration rates using the metabolic theory of ecology,

274 melatonin on total soluble solids and lower respiration rate was observed in both cultivars.

275 However, a progressive loss of ADP-dependent respiration rate was observed in intact enod93 mitochond

276 report that SOM decomposition or soil basal respiration rate was significantly affected by changes i

277 State IV mitochondrial respiration rates were 3.59 +/- 1.25 and 2.11 +/- 0.97 i

278 Soil respiration rates were 42-204% higher in warmed relative

279 Photosynthesis and respiration rates were also reduced in the DeltaCpcC1C2:

280 Interestingly, both pyruvate and glutamate respiration rates were decreased in TG mice.

281 three years, total microbial cell counts and respiration rates were highest in the GAC amended soil.

282 The carbohydrate and lipid state 3 respiration rates were lower in IUGR than CON, and CS ac

283 nd gene expression levels, calcification and respiration rates were measured relative to pHT 8.1 cont

284 atory differences became nonsignificant when respiration rates were normalized to the number of respi

285 to experimental warming such that leaf-level respiration rates were not increased.

286 Maximum mitochondrial respiration rates were significantly (p < 0.001) higher

287 NADH- and FADH(2)-linked maximal respiration rates were similar between lean and obese in

288 In contrast, state 3 respiration rates were similar in ob/ob and control mito

289 Daytime respiration rates were substantially higher than those m

290 t mitochondrial number, size, and fatty acid respiration rates were unchanged.

291 ed to low sulfate concentrations and/or high respiration rates, whereas fractionations greater than t

292 Inactivation of cytosolic PEPCK affected the respiration rate, which suggests that an excess of oxalo

293 arming (1-2 degrees C) had no effect on soil respiration rates, while +N addition and elevated CO2 co

294 ere more temperature sensitive and increased respiration rate with temperature increases to a greater

295 The negative correlation of the O(2) respiration rate with the surface/volume ratio is steepe

296 e simulated mass-specific soil heterotrophic respiration rates with multiple published datasets of me

297 acclimation of photosynthesis and increasing respiration rates with warming could possibly result in

298 ort the maximum NADH dehydrogenase-dependent respiration rate, with no upregulation of translation oc

299 oxygen concentrations suggest that microbial respiration rates within the plume were not appreciably

300 nied by increases in both photosynthesis and respiration rates, without affecting the activity of pho