ライフサイエンスコーパス: temperature

1 piration for a 10 degrees C increase in leaf temperature).

2 e following formula: (SBF37-SBFBT)/(37-basal temperature).

3 y Ar in 0% to 90% range controlled the flame temperature.

4 ivities of less than 1 W.m(-1).K(-1) at room temperature.

5 oth free and bound forms equally affected by temperature.

6 tors controls root responses to high ambient temperature.

7 ement to this end is through the increase of temperature.

8 croscopic quantum phenomena observed at room temperature.

9 rate constants (k) increased with the drying temperature.

10 affecting uniformity, scalability, or Curie temperature.

11 synapsis during male meiosis at high ambient temperature.

12 to soil water supply, atmospheric demand and temperature.

13 0) concentration of 260-300 mug/m(3) at room temperature.

14 zed, may exhibit paddlewheel dynamics at low temperature.

15 hich declined rapidly independent of storage temperature.

16 18% under continuous-wave condition at room temperature.

17 ngal as a triplet photosensitizer at ambient temperature.

18 2) display a bowl-to-bowl inversion at room temperature.

19 substrates, the reaction can proceed at room temperature.

20 ntiferromagnetic phases are bistable at room temperature.

21 litatively distinct effects depending on the temperature.

22 reversible structural transformation at room-temperature.

23 ing melting point and physical state at room temperature.

24 hat they are stable for up to 5 days at room temperature.

25 LG1 enhances the tolerance of plants to high temperature.

26 oil CO(2) efflux being out of sync with soil temperature.

27 egrees C increase in global mean surface air temperature.

28 ulating the phyB-PIF4 module at high ambient temperature.

29 hosting the quantum-spin-liquid state at low temperatures.

30 ying insect numbers on days with low ambient temperatures.

31 -but-1-en-3-ones with sodium azide at higher temperatures.

32 and resulting TE properties at the operation temperatures.

33 aining living cells are maintained at cooler temperatures.

34 nation to formate with faster rates at lower temperatures.

35 k in response time and stability at elevated temperatures.

36 ng thermofield double states at a variety of temperatures.

37 ellular phenotypes observed at nonpermissive temperatures.

38 the formation of a "buffer" against elevated temperatures.

39 us transport properties well above cryogenic temperatures.

40 +/- 0.01 and 0.39 +/- 0.01 at the aforesaid temperatures.

41 d strains were rapidly inactivated at higher temperatures.

42 ed from the heme iron by X-rays at cryogenic temperatures (100 K).

43 d in seven combinations of gradients of both temperature (11-37 degrees C) and oxygen saturation (17-

44 ree soaking times (0, 15, and 30 min), three temperatures (20, 25, and 30 degrees C) and four concent

45 rees C and 37 degrees C) and reduced at room temperature (22 degrees C).

46 ic ion concentration gradients (0-40 mM) and temperature (23-75 degrees C) is demonstrated here, show

47 Transmission is optimized at intermediate temperatures (23-26 degrees C) and often has wider therm

48 Moina dubia to lead (Pb, 50 mug/L) under two temperatures (25 and 28 degrees C) with/without predator

49 s and condensation is enhanced at human body temperatures (33 degrees C and 37 degrees C) and reduced

50 elial cells (HCEnCs) were exposed to various temperatures (4 degrees C, 23 degrees C, and 37 degrees

51 ge magnetic moment (0.5 mu(B) /Co) and Curie temperature (75 K), values larger than previously report

52 However, even at zero temperature, a fraction of the quantum liquid is excited

53 may relieve constraints of cooler night-time temperatures; a nuance that has largely been ignored in

54 iquid metal batteries need to be operated at temperatures above 240 degrees C to maintain the metalli

55 Storage temperature affected stability of anthocyanins, but had

56 ly varied over 3 orders of magnitude at room temperature and 6 orders of magnitude from 10 to 300 K.

57 introduced, which gives good results at room temperature and above, and for mobilities as low as 10(-

58 r physiologic evaluation of the mouse hotel, temperature and anesthesia were tested for uniformity in

59 ocomotor activity, along with increased body temperature and BAT gene expression, specifically Cox8b.

60 s, which are are routinely performed at room temperature and below, in materials with mobilities grea

61 icable to trap reactive intermediates at low temperature and creates a new method to characterize elu

62 These yields increase with increasing temperature and decrease with increasing excitation inte

63 microbes, which encompasses fluctuations in temperature and pH, as well as electron donor and accept

64 imate change transforms seasonal patterns of temperature and precipitation, germination success at ma

65 only when susceptible availability was high: temperature and rainfall had net positive and negative e

66 ticle metrics and MI cases, adjusted for air temperature and relative humidity.

67 fimide varied more than 10-fold depending on temperature and the site of the engineered methionine.

68 Changes in melting temperature and transitional pH depended on both the typ

69 respect to amorphous silica at pH = 9, room temperature and under anoxic conditions.

70 ed shortly after deposition was kept at room temperature and yielded 3.760 L of water, which was filt

71 gy, with structural fragility under the high temperatures and acidic environments of therapeutic appl

72 We found that warming soil temperatures and decreasing winter length have opposing

73 High temperatures and low humidity are common features of for

74 ly threatened by short-term exposure to warm temperatures and that longer-term physiological response

75 zation of 3.5 emu/cm(3) was observed at room temperature, and it retains ferromagnetic ordering in th

76 related with O(3), daily maximum and minimum temperature, and negatively correlated with atmospheric

77 of MeIQ formed increased with reaction time, temperature, and oxygen content in the reaction atmosphe

78 lasma separator tubes, storage-time, storage-temperature, and repeated freeze-thaw cycles on circulat

79 of pyrite significantly changes with the pH, temperature, and the ferric ion concentration, consisten

80 which was inversely correlated with maximum temperature, and the occurrence of Haemagogus and Sabeth

81 We analyzed coral bleaching, temperature, and turbidity data from 3,694 sites worldwi

82 iming of naive CD4 T cells in vitro at fever temperatures, and we report notable fever-mediated modul

83 eriments on phyllosilicates formed under low temperature aqueous conditons have illustrated that thes

84 ot and root growth responses to high ambient temperature are coordinated during early seedling develo

85 owever, the mechanisms by which plants sense temperature are not well understood.

86 night temperature is observed, wherein night temperatures are increasing at a higher pace and the tre

87 ficient electrocatalysts that operate at low temperatures are needed for electrocatalytic hydrogenati

88 shown to exhibit a zero-bias anomaly at low temperatures, arising from a suppression of the quantum

89 cess to both traditional C-N adducts at room temperature as well as a large range of previously inacc

90 cs of climate en route to stable global mean temperature at 1.5 and 2 degrees C above preindustrial l

91 de substitution stabilizes Boat, spiking the temperature at which Boat and Chair can readily intercha

92 We have also developed a temperature-based screening method for synthetic paralys

93 verwinter, animals must detect constant cold temperatures before adapting their behavior accordingly.

94 Furthermore, at the lowest temperatures, below the susceptibility maximum, we obser

95 s are shown for stars with stellar effective temperatures between 2,600-9,000 K.

96 to facilitate transition through the gateway temperatures between 80 and 85 degrees C.

97 In contrast, at higher temperatures, both clv2/crn signaling and heat-induced a

98 Respiration acclimated to elevated temperatures, but there were no treatment effects on the

99 e assembly kinetics and increase the optimal temperature by circa 4-7 degrees C for isothermal assemb

100 ly determined during growth but also at room temperature by post-processing.

101 onmental changes, such as varied sea surface temperatures caused by storms.

102 During a brief increase in temperature, cells undergoing spermatogenesis, but not o

103 F-causing variant, and confirm rescue by low temperature, CFTR-targeting drugs and second-site revert

104 nally, we are able to predict accurately the temperature change in the North Atlantic.

105 kos, and other invasive species globally, as temperatures change.

106 d receptors, act as the initial detectors of temperature changes across taxa.

107 pling, which can alter deforestation-induced temperature changes.

108 eased by >0.5 degrees C more than night-time temperatures, cloud cover, specific humidity and precipi

109 For annual plants, higher temperatures, CO(2) and drought stress increase foliar h

110 up to 242 degrees C and a 7500-oersted room-temperature coercivity.

111 formidable challenge, especially under high-temperature conditions.

112 Based on such temperature control strategy, NGD sensitivity and the dy

113 Although temperature controls the storage of soil organic carbon

114 ted a multi-responsive hydrogel that, at one temperature, could be moved through a constriction under

115 tion under a magnetic field and, at a second temperature, could grip and transport a cargo.

116 rogressively longer times we find an ambient temperature decay time of the Omega Fe-C5' bond of tau ~

117 Elevated temperatures decreased (P = 0.026) placental mRNA expres

118 exible chains; the network topology freezing temperature decreases with increasing MW of flexible lin

119 ey rules of life and their interactions: the temperature dependence of biotic processes from enzymes

120 The temperature dependence of ordered domain formation was m

121 sensitivity, precision, dynamic ranges, and temperature dependence of such sensors.

122 e observe a regime characterized by a linear temperature dependence of the inverse susceptibility tha

123 bility that differs sharply from the quartic temperature dependence predicted by the LKSR theory.

124 Different temperature dependent band splitting behaviors are obser

125 single-molecule manipulation studies of the temperature dependent unfolding and refolding of a titin

126 We attribute a major role to post-melting temperature-dependent diffusion of hydrogen occurring ab

127 bent assay (ELISA)-based assay that uses the temperature-dependent loss of conformational epitopes to

128 The temperature-dependent migration of molecular weight prot

129 together, these results identify a plausible temperature-dependent molecular mechanism, which contrib

130 nd molecular-dynamics simulations reveal the temperature-dependent morphological changes in poplar wo

131 However, S. carpocapsae IJs exhibited a temperature-dependent quiescent period.

132 lted in irreproducible entropy change versus temperature diagrams, which was attributed to the releas

133 tegrated on flexible polymers, enhanced room-temperature dielectric permittivity with large mechanica

134 apable of predicting accurately moisture and temperature distributions along with heath beneficial co

135 a given material in the wide pressure-volume-temperature domain even if its typical form with constan

136 sing data-constrained modeling, we find that temperature-driven increases in trophic transfer efficie

137 or in the presence of glycine under moderate temperature drying conditions.

138 dynamically adjusted to any change in pH and temperature during the sport practice by means of a new

139 ites can be very important, we need to study temperature effects on host-parasite dynamics in a commu

140 Notably, however, the room-temperature emission efficiency and the fluorescence lif

141 triggered BPM1 degradation, whereas elevated temperature enhanced BPM1 stability and accumulation in

142 glendonite calcite, to generate quantitative temperature estimates for northern mid-latitude bottom w

143 Prolonged high-temperature extreme events in the ocean, marine heatwave

144 However, no spontaneous room-temperature ferroic property has been observed to date i

145 Our recent discovery of the strong room temperature ferromagnetism in single layers of VSe(2) gr

146 Plants have to interpret temperature fluctuations, over hourly to monthly timesca

147 variation could be prevented by altering the temperature for growth.

148 ents were those that had the highest optimal temperatures for photosynthesis, implying that the syner

149 ide range of relative humidities (0-90%) and temperatures ([Formula: see text]) using gravimetric typ

150 k(ex) values were measured as a function of temperature from 5 to 45 degrees C to determine the ther

151 against multiple reconstructions of surface temperature from tree-ring records, we find little evide

152 conductivity is favorable for preserving the temperature gradient between the two ends of a thermoele

153 rthern hemisphere create an interhemispheric temperature gradient that enhances the southward cross-e

154 ion vessel (the "saturator") to minimize the temperature gradients and internal volume, (2) the use o

155 urface temperature thresholds or inter-ocean temperature gradients.

156 illiseconds for cavity-coupled ions, even at temperatures greater than one kelvin.

157 The temperature had a small effect on recovery, but signific

158 usly difficult-to-study drug targets at room temperature, has now been adapted for use in synchrotron

159 These findings infer that elevated temperatures have a profound impact on global N cycling

160 bial species, organisms adapted to different temperatures have measurable differences in DNA, RNA and

161 Such near-freezing temperatures have not previously been reconstructed from

162 s manipulation could be accomplished at room temperature; hence this opens avenues for magnetooptical

163 The rapid increase of global temperatures highlights the need for a clear assessment

164 ebral blood flow (CBF), as well as core body temperature; however, the isolated influence of temperat

165 igh pH and exposure to extreme variations in temperature, humidity and irradiation.

166 cted that COVID-19 would decline with higher temperatures, humidity, and ultraviolet (UV) light.

167 ange of chloroarenes with B(2)pin(2) at room temperature in excellent yields and with high selectivit

168 ity measured in mOmega cm, T is the absolute temperature in K, S is the Seebeck coefficient, and k(B)

169 Meal ingestion increases body temperature in multiple species, an effect that is blunt

170 echnique could be used to determine the bulk temperature in transient systems with a temporal resolut

171 ng both egg TH levels and post-hatching nest temperature in wild pied flycatchers (Ficedula hypoleuca

172 that stabilizes sub-100 nm skyrmions at room temperature in zero field.

173 of 2.9 x 10(-24) N m Hz(-1/2) at millikelvin temperatures in a dilution refrigerator(6).

174 -trans (1ct) product conformers at cryogenic temperatures in a N(2) matrix, and subsequent narrow-ban

175 The results showed that warm temperatures in spring had a positive effect on NEP in c

176 In the grassland, record-breaking temperatures in the winter of 2015/2016 led to a Februar

177 ng in the presence of NaSCN decreased as the temperature increased.

178 behaviours showed significant changes as the temperature increased.

179 Conversely, where daytime temperatures increased by >0.5 degrees C more than night

180 f a current can be different at high and low temperatures, indicating that even a well-defined geneti

181 Our results establish that air temperature is a necessary but not sufficient variable f

182 fferential rate of increase in day and night temperature is observed, wherein night temperatures are

183 Temperature is one of the most impactful environmental f

184 Below a lower critical solution temperature (LCST), they are highly soluble.

185 % of potassium carbonate, or at electrolysis temperatures less than 700 degrees C.

186 o realizing a stable Li metal anode for high-temperature Li metal batteries with a simple battery con

187 n be facilely operated for rechargeable high-temperature Li metal batteries.

188 ng environmental stressors, including CO(2), temperature, light, and nanoplastics.

189 raction are large body mass, increase in air temperature, loss of natural land, and high human popula

190 vation streams, which include low but rising temperatures, low oxygen supply and increasing oxygen de

191 The land surface temperature (LST) changes in North America are very abno

192 stable to catalyze methane combustion at low temperatures (<500 degrees C) with a low light-off tempe

193 s calculations to uncover the origin of high-temperature magnetism in these superlattices and the cha

194 Some of the best-performing high-temperature magnets are Sm-Co-based alloys with a micros

195 ergy production), and the high pressures and temperatures make NH(3) production facilities very expen

196 Targeted temperature management in comatose survivors of out-of-h

197 sists despite a strictly protocoled targeted temperature management.

198 of sustained global warmth with mean global temperatures markedly higher (by ~2-3 degrees C) than to

199 flow) is preserved during both exercise and temperature-matched passive heat stress ABSTRACT: Acute

200 pling during submaximal cycling exercise and temperature-matched passive heat stress during isocapnia

201 ld constant) Submaximal cycling exercise and temperature-matched passive heat stress provoked ~16% in

202 mple stability, heatsink considerations, and temperature measurement and feedback.

203 bout symptoms and travel history, as well as temperature measurements.

204 hylaxis, reflected by increased drop in body temperature, most likely due to accelerated histamine-in

205 spectral peak that appears in global surface temperature observations appears to reflect the response

206 atures (<500 degrees C) with a low light-off temperature of 230 degrees C and 100% selectivity to CO(

207 and 20% initial soluble solids at an optimal temperature of 30 degrees C.

208 s along with the onset, peak, and conclusion temperatures of gelatinization were increased.

209 The gelatinization temperatures of the modified starches were similar to th

210 e to experimentally determine optimal growth temperature (OGT) for every known microbial species, org

211 perature; however, the isolated influence of temperature on CBF regulation during exercise has not be

212 ined effects of water content, body size and temperature on plant metabolic rates.

213 An Eyring analysis, examining the effect of temperature on the propagation rate coefficient (k(p)),

214 specific physical conditions of high or low temperature or high pressure.

215 t find any correlations with climate/daytime temperatures, or region.

216 ly have reduced recruitment given forecasted temperatures over future decades.

217 The observed interactive effects of temperature, oxygen availability, and body size predict

218 The temperature parameter as originally calculated for the P

219 Whereas temperature partially constrains Leucocytozoon diversity

220 including type of mixing solvent, substrate temperature, particle concentration, and assembly time i

221 Gamma point of the energy bands of the high-temperature phase is lifted in the low-temperature phase

222 high-temperature phase is lifted in the low-temperature phase.

223 However, it is hard to achieve a room temperature phosphorescence material with simultaneous l

224 Room temperature photolysis of the bis(azide)cobaltate(II) co

225 ng different GHG metrics (global warming and temperature potentials) and time horizons (20 and 100 ye

226 ons are causing concurrent shifts in CO(2) , temperature, precipitation regimes and nitrogen depositi

227 ested whether species' responses to changing temperatures predicted their population trends from a UK

228 However, the high processing temperatures prevent growth of other Janus materials and

229 in a single assay; and operates at elevated temperatures, providing high selectivity and compatibili

230 and it retains ferromagnetic ordering in the temperature range 5-395 K.

231 nt free to bound forms ratio showed that the temperature range tested had a minor effect on bound-for

232 of a touch sensor operational across a wide temperature range, including freezing conditions, is dem

233 th the tools to analyze proteins over a wide temperature range, paving the way toward T-dependent hig

234 ample, we identify different pressure-volume-temperature ranges within which molecular dynamics is do

235 he formation of spin fluctuations in the low-temperature regime.

236 and streams will experience major changes in temperature regimes, absolute and relative inputs of sol

237 ssible role in contributing to Earth surface temperature regulation.

238 e gradients and regional variations in brain temperatures reported in the literature for awake animal

239 region of the trimeric serine hydrolase high-temperature requirement 1 (HTRA1) are associated with in

240 Here, we estimated the temperature response of g(m) , g(bs) and leakiness ( ),

241 our model simulations support a surface air temperature response to the eruption of the order of -1

242 tratospheric ozone, possibly due to a global temperature rise.

243 istribute poleward or into deeper water when temperatures rise because of barriers, reduced light ava

244 ), under different technological conditions (temperature, roasting, use of whole nuts, screw speed an

245 Using a temperature-sensitive allele (Sac1(ts)), we show that Sa

246 ght sensitivity using gold nanorods bound to temperature-sensitive engineered transient receptor pote

247 rmal gradients by changes in fluorescence of temperature-sensitive fluorescent dyes need to account f

248 inner membrane 23 is compromised such as in temperature-sensitive mutants of Tim17.

249 Here, we examine the temperature sensitivity of phenology, and highlight cond

250 Whereas spatial temperature shifts have been studied extensively in the

251 However, the dynamic effects of temperature shifts have remained mostly unstudied at the

252 owever, the mechanisms integrating light and temperature signaling pathways in plants remain poorly u

253 trispyrazoylborate) system as a function of temperature, solvent, ancillary ligand, and arene substi

254 have investigated the effect of the reaction temperature, solvent, substituent, and type of reducing

255 rface salinity (delta(18)Ow) and sea surface temperatures (SSTs) from the Bay of Bengal (BoB).

256 are excellent candidates owing to their high-temperature stability.

257 dropwise condensation of water vapor on low-temperature substrates.

258 thermal reaction norm slopes at high ambient temperatures, suggesting that the current level of therm

259 ction between sportfish predation and warmer temperatures suggests redundancy of their size-selective

260 e moderate-intensity exercise increases core temperature (T(c) ; +0.7-0.8 degrees C); however, such e

261 oefficients from these models, i.e. critical temperature (T(crit) ) and the initial response (m(1) ),

262 ions on crystallisation and glass transition temperature (T(g)) of three Chilean dried raisins were e

263 The basal muscle temperature (T(m) ) was lower in PAD rats than in contro

264 ere characterized based on the maximum flame temperature (T(max,c) ~ 1791 to 1857 K) and the highest

265 57 K) and the highest soot luminosity region temperature (T*(c) ~ 1600 to 1650K).

266 dependence of the superconducting transition temperature, T(c), near to optimal doping that sheds lig

267 sal activity and agonist sensitivity at room temperature than the Pro to Gln substitution in the extr

268 ow statistically significant increases, with temperatures that are consistent with activation energy

269 Increasing frequencies of temperatures that exceed historically observed tolerance

270 Short photoperiod and low temperature, the major seasonal cues heralding winter, s

271 unneling has been invoked to explain the low-temperature thermal conductivity of solids for decades,

272 A series of cut off temperature thresholds and durations (2, 3, and 4 consec

273 Temperature thresholds for PM transition from low to hig

274 cts were predominantly driven by sea-surface temperature thresholds or inter-ocean temperature gradie

275 by using engineered channels with different temperature thresholds.

276 ing formalism for the quantification of high-temperature transition aluminas.

277 were subjected to one of three acute (24 h) temperature treatments: cold stress (18 degrees C), heat

278 Thus, explaining the North Atlantic temperature trends and particularly the NAWH requires co

279 warming, relative to the background positive temperature trends, often dubbed the North Atlantic warm

280 At lower temperatures triplet-triplet annihilation dominates.

281 on a scale-model building) below the ambient temperature under a solar intensity of 744 W m(-2) (850

282 in shear rate and declined by increasing the temperature up to 50 degrees C.

283 metal-organic ferrimagnets feature critical temperatures up to 242 degrees C and a 7500-oersted room

284 scribe, depending on the metal and synthesis temperature used, as random (Co, Cd, 120 degrees C), sho

285 ght-induced tuning of ferromagnetism at room temperature using a halide perovskite/oxide perovskite h

286 differently as DTW results in greater daily temperature variation and moves organisms nearer to thei

287 )O record for global ice volume and deep-sea temperature variations.

288 Body temperature was associated independently with clinically

289 s in their response times, a clear effect of temperature was present in both behaviours.

290 Temperature was the main driver of adaptation, resulting

291 tin fractions respectively extracted by room temperature water, 90 degrees C-water, CDTA and Na(2)CO(

292 precipitation of driest quarter, annual mean temperature, water vapor, and precipitation during the c

293 y photoemission spectroscopy below the Curie temperature, we observe topological Fermi arcs that corr

294 conditions (high speed, low visibility, low temperature, wet track).

295 uccess at higher and lower natural ranges in temperature, when blowfly larvae are more potent rivals

296 responding heterodiene structure at elevated temperature, which was used to generate six-membered pho

297 ecipitation, germination success at marginal temperatures will become critical for the long-term pers

298 ion, increases significantly with increasing temperature, with an adsorption enthalpy (DeltaH(ads)) o

299 semblies reveal Curie-Weiss behavior at high temperatures, without pairing of the 5f(2)-electrons dow

300 y of single-atom Fe(1)(II)-N(4) sites via in-temperature X-ray absorption spectroscopy.