ライフサイエンスコーパス: light intensity

1 ession in the middle of the day dependent on light intensity.

2 ect) can also be enhanced by a change in the light intensity.

3 in sample thickness, dye concentration, and light intensity.

4 to reduced recombination loss under diluted light intensity.

5 oplast performance in response to changes in light intensity.

6 quinol is possible after a rapid increase in light intensity.

7 rate can be tuned: it is linearly related to light intensity.

8 of the fluorescence signal on the excitation light intensity.

9 otosynthesis-related processes to changes in light intensity.

10 tyl elongation depends on the day length and light intensity.

11 ative demand as well as dynamic responses to light intensity.

12 narrowband gamma oscillation increased with light intensity.

13 initiate reversals in response to changes in light intensity.

14 roplast function to unpredictable changes in light intensity.

15 ght intensity, or combined high CO2 and high light intensity.

16 of reaction can be controlled by varying the light intensity.

17 al D1 protein turnover under moderate growth light intensity.

18 on of CAO expression as a function of growth light intensity.

19 bute to the response over several decades of light intensity.

20 enters in var1 or var2 under moderate growth light intensity.

21 the rate of the reaction is dependent on the light intensity.

22 in response to environmental fluctuations in light intensity.

23 of reactions by which rods signal changes in light intensity.

24 s by manipulating symbiont load according to light intensity.

25 mediate light levels and were lowest at high light intensity.

26 and respond to the daily changes in ambient light intensity.

27 em I for the first seconds after a change in light intensity.

28 cell elicited exocytosis that was graded to light intensity.

29 preventing state transitions upon changes in light intensity.

30 ntal factors such as temperature and average light intensity.

31 anism for enabling visual orientation at any light intensity.

32 -resolution imaging of living cells with low light intensity.

33 sponse to nitrogen starvation and changes in light intensity.

34 n pupillary constriction with increasing log light intensity.

35 ctor of approximately 5, independent of bias light intensity.

36 with control plants under conditions of high light intensity.

37 takes place when plants are shifted to lower light intensity.

38 rent growth-associated pathways to increased light intensity.

39 preventing state transition upon increase in light intensity.

40 ol cells, which are excited by increments in light intensity.

41 tuations of multiply scattered near-infrared light intensity.

42 nce both negligible photothermal heating and light intensity.

43 vel response to light quality independent of light intensity.

44 gulation during developmental acclimation to light intensity.

45 ndent electron sinks during rapid changes in light intensity.

46 ch the hole transport time is independent of light intensity.

47 potential of this reagent is tunable by the light intensity.

48 e, flow rate, initial water temperature, and light intensity.

49 imaged size of the beam spot with decreasing light intensity.

50 re on temperature, and therefore on incident light intensity.

51 and dynamics in response to changes in white light intensity.

52 usage for cells acclimated to four different light intensities.

53 photosynthetic activity over a wide range of light intensities.

54 otoreceptor subtypes to respond to different light intensities.

55 arkable breadth of spatiotemporal scales and light intensities.

56 mization of photosynthesis under fluctuating light intensities.

57 lation activation occurs already at moderate light intensities.

58 s may be achieved using higher (16-33%) blue light intensities.

59 (RWCs), COS concentrations, temperatures and light intensities.

60 aches the photoreceptor according to ambient light intensities.

61 de irradiance across a wide range of ambient-light intensities.

62 he retina enable vision over a wide range of light intensities.

63 cells to encode motion over a wide range of light intensities.

64 states allowing plants to survive under high light intensities.

65 mals must operate under an enormous range of light intensities.

66 r natural viewing conditions and at moderate light intensities.

67 siological hyperpolarization of cells at low light intensities.

68 itch exclusively to polarized light at lunar light intensities.

69 s and drives dopamine release at very bright light intensities.

70 rameters and map the results against varying light intensities.

71 whether their expression responds to altered light intensities.

72 mples in the dark but slows again for higher light intensities..

73 te of (PSII) decline across a large range of light intensities (0-1,000 mumol photons m(-2) s(-1); be

74 ntum yield was as high as 0.73, and moderate light intensity (10(2) mumol.m(2).s(-1)) is sufficient f

75 spend hours per day exposed to intermediate light intensities (30-300 lux), particularly in the even

76 growth temperature (3 vs. 18 degrees C) and light intensity (30 vs. 40 mumol quanta.m(2).s(-1)), whi

77 of topological properties by a change in the light intensity(7,12) and can break optical reciprocity(

78 Modulations in light intensity across a visual image could be caused by

79 N cells are capable of reporting the average light intensity across the whole visual field.

80 r-based measurements suggest that increasing light-intensity activity and reducing sedentary time are

81 moderate-intensity activity over one day and light-intensity activity over three days induce a transi

82 rmore, system settings such as the measuring light intensity affected F (0), F(m) , and F(v) /F(m) in

83 summer conditions of cycling temperature and light intensity, an additional prominent afternoon (A) c

84 They operate over a similar range of light intensities and adapt to backgrounds and bleaches

85 rctic domain, fungal parasitism is linked to light intensities and algal stress that can elevate dise

86 nities and are linked in their occurrence to light intensities and algal stress.

87 esponse of most light-driven polymers to low light intensities and by the lack of controlled multisha

88 and absorbance spectroscopy under different light intensities and CO2, to test predictions of the mo

89 light-responsive gripper is sensitive to low light intensities and has programmable states and rapid

90 Growing conditions combining high light intensities and low temperatures lead to anthocyan

91 ranching or tillering in response to varying light intensities and ratios of red and far-red light ca

92 of the cells resembling that induced by high light intensities and therefore triggers high light prot

93 was observed that excluding low fluorescent light intensity and air by vacuum packaging at 20 degree

94 As noon approaches and light intensity and ambient temperature tend to increase

95 CC 6803 moves with Type IV pili and measures light intensity and color with a range of photoreceptors

96 low (LL), moderate (ML) and high (HL) growth light intensity and correlated these with key photosynth

97 oplast performance in response to changes in light intensity and darkness.

98 e evaporation rate increased with increasing light intensity and decreased with increasing salinity.

99 light harvesting components with increasing light intensity and growth rate.

100 is known about the neural representation of light intensity and how it covers the necessary range.

101 PQ allows for a rapid response to changes in light intensity and in vascular plants, is primarily tri

102 onveys information about changing background light intensity and increases the signal:noise for fast

103 conds as a graded response to changes in the light intensity and ionic composition of the medium and

104 antly influenced by the interactions between light intensity and maternal wing morphs.

105 The higher light intensity and NO3-N concentration in Muskegon Lake

106 n by measuring the dependence of its rate on light intensity and point mutations.

107 duce how the rotational frequency depends on light intensity and polarization.

108 Reversals were modulated by changes in light intensity and preceded by the migration of HmpF-GF

109 ell-known dose-response relationship between light intensity and pupil contraction.

110 sed to characterize the relationship between light intensity and pupillary response.

111 MT9 gene was found to be upregulated by high light intensity and salt stress.

112 zed as an exponential decline under changing light intensity and soil moisture.

113 We analyzed light intensity and temperature data obtained from geolo

114 tially underlying the computation of ambient light intensity and temporal light changes already withi

115 associated with protection from UV and high-light intensity and the genes suppressed after 7 days of

116 The higher light intensity and total nitrogen concentration may hav

117 na membranes occurs under conditions of high light intensity and triggers a major photoprotection mec

118 e high WUE trait was resilient to changes in light intensity and water availability, but it was sensi

119 Tuning the light intensity and wavelength of the irradiation can re

120 photon excitation is studied by varying the light intensity and wavelength, but under no significant

121 field light signals (like short photoperiod, light intensity and/or light quality) before the low tem

122 e displayed leaf rolling in response to high light intensity and/or low humidity.

123 e in physical activity volume, time spent in light-intensity and moderate- to vigorous-intensity phys

124 Different scenarios of energy availability (light intensity) and demand (source leaf versus a growin

125 . PCC 6803 under different nitrogen sources, light intensities, and CO2 concentrations.

126 ies are limited by long reaction times, high light intensities, and/or large catalyst loadings.

127 owed only minor changes upon fluctuations in light intensity, and (3) absence of STN8 completely abol

128 dependent on environmental factors, such as light intensity, and could be exploited to improve crop

129 s, especially under low light or fluctuating light intensity, and in a short day photoperiod compared

130 agonal-to-cross-peak ratio on concentration, light intensity, and mixing time.

131 as a function of the ink composition, the UV light intensity, and the velocity of the liquid jet, ena

132 s method is capable of reducing the required light intensity, and thus minimizing the photothermal da

133 ted substantial variation driven by T(air) , light intensity, and vapor pressure deficit, and T(leaf)

134 n are established between average night-time light intensity (ANLI) and average commercial residentia

135 simple linear regression model based on UVB light intensity appears to be a useful tool for predicti

136 nts and dynamic responses to step changes in light intensity are assessed.

137 Parameters such as photon stoichiometry and light intensity are highlighted within to inform future

138 Short-term reactions to changing light intensity are triggered inside chloroplasts and le

139 g the OS does not increase linearly with the light intensity as with diffuse light.

140 More evening-types had higher light intensity at 2 h before sleep and lower melatonin

141 The sample temperature and the incident light intensity at 355 nm tune the characteristic switch

142 by which ipRGCs encode variations in ambient light intensity at these early ages are not known.

143 Irrespective of the light intensity at time of harvest, the highest leaf dry

144 Large antennae are disadvantageous at low light intensities because they increase excitation energ

145 o reversible phosphorylation upon changes in light intensity (being under control of redox-regulated

146 the transmission of a physical quantity, say light intensity-between any two points in space is ident

147 rs are then used to causally estimate random light intensities both at the front and back end of the

148 by the temperature, CO(2) concentration and light intensity but also the spectrum of light.

149 ow visual neurons enhance sensitivity at low light intensities, but they could pose a challenge for m

150 not respond to a spatiotemporal gradient in light intensity, but rather they directly and accurately

151 cumulation during exposure of plants to high light intensity by modulating the expression of transcri

152 shoot-to-root ratio in response to changing light intensities, by modulating root growth.

153 ereas hosts benefited from symbiosis at high light intensity, carrying endosymbionts was costly to ho

154 vation energy and super-linear dependence on light intensity cause the unheated photocatalytic methan

155 le reasons for the otherwise mild effects of light intensity changes on gene expression in differenti

156 ng in thylakoid protein phosphorylation upon light intensity changes, the excitation balance between

157 ed, such as under salt stress or upon sudden light intensity changes.

158 s lost after prolonged incubation under high light intensity conditions.

159 ere well correlated to the daily average UVB light intensity corrected for light screening incorporat

160 ne a 66-dimensional space of local grayscale light-intensity correlations, and measure the relevance

161 that transcriptional responses to changes in light intensity could occur within seconds, rates for wh

162 lysed with a bioluminescent method using the light intensity decay constant.

163 Growth under reduced light intensity delays both the decline in miR156/157 an

164 High and low light intensities, delivered via a realistic dynamic flu

165 so exhibited the quadratic increase with the light intensity, demonstrating the effectiveness of the

166 This study addresses the light intensity dependence of charge accumulation in a p

167 scence imaging technique, to investigate the light-intensity dependence, kinetics, reversibility, and

168 entration of light, as we determine from the light-intensity-dependent activity in the plasmon-excita

169 )(-) uptake of Chamydomonas reinhardtii in a light-intensity-dependent manner.

170 by temperature-dependent photoluminescence, light-intensity-dependent time-resolved photoluminescenc

171 ient light sensor (ALS) of the smartphone as light intensity detector and its LED flash light as an o

172 non-binding states under red light, with the light intensity determining the cycling rate and thus th

173 On the other hand, under 37-fold lower light intensity, different, less stable and change-resis

174 Even at lower light intensities, diffuse light photosynthesis was equa

175 rent signals exhibit similar patterns to the light-intensity distribution of the waveguide calculated

176 n the microenvironmental levels of CO(2) and light intensity during cell growth, revealing cellular s

177 re likely to experience caused by changes in light intensity during daylight.

178 ave been studied by changing constant growth light intensity during the day, responses to fluctuating

179 a dynamic response to small fluctuations in light intensity during the day.

180 ff cells respond more strongly to changes in light intensity during the subjective night than during

181 ve fields and preclude any bias toward local light-intensity fluctuations.

182 ght-harvesting pigments and require a higher light intensity for saturation of photosynthesis.

183 dimming range with the relative transmitted light intensity from 0.17 to 0.72 can be achieved at low

184 ength of the PC nanostructure, the reflected light intensity from the PC is dramatically and locally

185 Animals use vision over a wide range of light intensities, from dim starlight to bright sunshine

186 can be controlled by three parameters: input light intensity, gain and loss amplitude, and input beam

187 e the mechanisms of long-term acclimation to light intensity have been studied by changing constant g

188 ing the day, responses to fluctuating growth light intensity have rarely been inspected in detail.

189 d into visual nerves to adjust environmental light intensities, have been one of the serious challeng

190 It is demonstrated that the influence of light intensity I can be included in the model in a powe

191 chamber experiments irradiated with varying light intensities in order to mimic realistic indoor lig

192 chiometry, evolutionarily adapted to the low light intensities in the habitat of purple bacteria, is

193 phenotypic growth defects observed under low light intensities in the presence of glucose, whereas un

194 ruitment of NMDARs is important for encoding light intensity in retinal ganglion cells.

195 ipRGCs contribute to the proper encoding of light intensity in the developing retina.

196 response and 50% modulation of the reflected light intensity in the near infrared part of the spectru

197 The pace of the clock is insensitive to light intensity in YHB plants, indicating that light inp

198 mouse retinas under physiologically relevant light intensities, in an intensity-dependent manner, wit

199 ty of reflex responses to changes in ambient light intensity, including circadian photoentrainment.

200 e transitions from extrinsic to intrinsic as light intensity increases.

201 ON) and outer (OFF) sublayers in response to light intensity increments and decrements, respectively.

202 nimals estimate visual motion by integrating light intensity information over time and space.

203 onstruction without considering the absolute light intensity information.

204 We show a new pathway for integrating light-intensity information into the clock network, sugg

205 Background light intensity (irradiance) substantially impacts the v

206 ut very high amplitude changes in background light intensity (irradiance).

207 y superior to previous reports and at higher light intensities is paving the way toward the potential

208 her-order resonant mode under a low incident light intensity is demonstrated.

209 TP production rate as a function of incident light intensity is determined after identifying quinol t

210 How light intensity is perceived, and how long the ROS wave

211 is to respond rapidly to these variations in light intensity is restricted by the relatively slow ope

212 In particular, high light intensity is shown to affect lipid biosynthesis, i

213 Here, we show that solely increasing light intensity leads to an increased midday siesta in D

214 Perception of a change in light intensity leads to the activation of multiple phys

215 extremity movements, sound pressure levels, light intensity level, and visitation frequency.

216 generating significant photocurrent at white light intensity levels close to ambient daylight conditi

217 rences could be detected comparing different light intensities, light exposure times or riboflavin co

218 selected leafy vegetables in relation to the light intensity (low and high Photosynthetically Active

219 ation rates were achieved with extremely low light intensities (<1 mW/cm(2)) and catalyst loadings (<

220 are dependent on particle concentration and light intensity, making it highly controllable.

221 modulation of TCP15 activity in vivo by high light intensity may serve to adjust anthocyanin accumula

222 m yielded OH radical peak values at moderate light intensity measured at evenings of 1.8 x 10(6) cm(-

223 s (typically considered to encode background light intensity) modestly over that encountered during s

224 onances, followed by a multifold increase in light intensity modulation.

225 key contributor to circadian assessments of light intensity, most efficiently captures photons aroun

226 hough direction selectivity is robust across light intensities, motion discrimination for OFF signals

227 For this, the applied light intensity must be sufficient to guarantee the stat

228 Light intensities of 10, 30, and 50 lux resulted in late

229 ata, in particular under high (de)excitation light intensities of super-resolution imaging or in sing

230 endence of the response of NPQ to changes in light intensity on the presence and accumulation of zeax

231 addition appears to reinforce the effect of light intensity on the quantity of photoassimilates avai

232 an induce large and frequent fluctuations in light intensity on the retina.

233 r dynamic field conditions (i.e. fluctuating light intensities or temperatures).

234 Changes in light intensity or quality induce changes in the reducti

235 ether 1) replacing total sedentary time with light-intensity or moderate to vigorous physical activit

236 rrupted sitting and sitting interrupted with light-intensity or moderate-intensity walking every 20-m

237 tabolism was limiting, such as low CO2, high light intensity, or combined high CO2 and high light int

238 evels in depressed patients and the temporal light intensity patterns of distant stars.

239 Light intensities (photons s(-1) mum(-2) ) in a natural

240 Above a threshold light intensity, photosynthetic electron transport rates

241 % CI, 5.0-7.8]; P < .001), 4.6 vs 3.8 h/d of light-intensity physical activity (difference, 0.8 [95%

242 Acclimation to changing light intensities poses major challenges to plant metabo

243 accumulation dynamics over a broad range of light intensities proves that the classic Keller-Segel m

244 ilms in microcosms grown under a gradient of light intensities (range: 5-152 mumole photons s(-1) m(-

245 e photoreceptors support vision across large light intensity ranges.

246 quire that the object is trapped at the high-light-intensity region.

247 currents at less than one-thousandth of the light intensity required by previously available optogen

248 kinetics at less than one-thousandth of the light intensity required by the most efficient currently

249 The acclimation of plants to changes in light intensity requires rapid responses at several diff

250 thod provides a powerful alternative for low light intensity RESOLFT nanoscopy, which enables biologi

251 mitation, quorum sensing, light quality, and light intensity (self-shading) were not the main factors

252 or copious numbers of pair creation requires light intensities several orders of magnitude higher tha

253 sing scheme to quantify consistent reflected light intensity signals under variable lighting and chan

254 med into having an exponential dependence on light intensity, similar to that observed in TiO(2)-base

255 A power function (light intensity) simulation of elastic Mie scatter confi

256 Light intensity, spectra, and timing are important for S

257 rescence parameters under a range of actinic light intensities (steady-state fluorescence yields, Ft

258 Its contraction was modulated in terms of light intensity, stimulation frequency, and t(on)/t(off)

259 We demonstrate that natural changes in light intensity substantially affect the expression of h

260 rostheses, allowing them to be used at lower light intensities such as those encountered in everyday

261 The OCP-TMR complex was sensitive to the light intensity, temperature, and viscosity of the solve

262 gnal to noise for a given average excitation light intensity than sinusoidally-modulated illumination

263 phonull animals is only observed at brighter light intensities that activate melanopsin phototransduc

264 anopsin phototransduction, but not at dimmer light intensities that activate only the rod/cone pathwa

265 ntrc is highly sensitive to rapidly changing light intensities that probably do not involve the chlor

266 ," a specific nonlinear response function to light intensity that drives algae toward beneficial ligh

267 h after dawn and in response to decreases in light intensity that occurred >10 h after dawn.

268 When grown under fluctuating light intensities, the Arabidopsis MET1 null mutant (met

269 Following decreases in light intensity, the rate of accumulation of starch decl

270 sis is accelerated in response to increasing light intensity, thereby enhancing the carbon fixation a

271 Thermal time and sum of light intensity thresholds were different to achieve the

272 e in enabling plants to adapt to fluctuating light intensity through a mechanism distinct from photos

273 By experimentally manipulating light intensity through the application of shading, we s

274 lular functions under conditions of very low light intensities to avoid photodamage to the cell and r

275 negative phototactic mutant required higher light intensities to evoke ChR1 phosphorylation.

276 mouflage that requires adjusting the organ's light intensity to "hide" their silhouettes from predato

277 nversion rate and require a 2.5 times higher light intensity to reach maximum photosynthetic efficien

278 rameters (e.g., capillary length, flow rate, light intensity) to identify printing conditions that we

279 al. (2017) show that increases in background light intensity trigger proportional increases in narrow

280 tures showed two-fold increase in diffracted light intensity under monochromatic light illumination.

281 ved between study sites with different night-light intensity used as proxy for urban development.

282 urons in the retina signal graded changes in light intensity via sustained release of neurotransmitte

283 hree days of either uninterrupted sitting or light-intensity walking interruptions (n = 5).

284 Light intensity was a strong predictor of pupillary resp

285 Over time (1992-2012), an increase in mean light intensity was found for the ranges of the majority

286 s of starch occurred if the same decrease in light intensity was imposed more than 10 h after dawn.

287 at a chloroplast transcriptional response to light intensity was mediated by SIG5; a chloroplast tran

288 temperature, we measured other factors (e.g. light intensity, water motion, nutrients, sea urchin den

289 s grown for various times under a variety of light intensities, we demonstrate that AHA2 localization

290 ntal conditions render diurnal variations in light intensity weak/ambiguous sources of timing informa

291 tant communities that established under high-light intensities were dominated (>90% of metagenomic re

292 Cultivars capable of higher ETR at midrange light intensities were shown to produce greater leaf are

293 Under low light intensities, where only synaptically driven rod/co

294 rella densities increased monotonically with light intensity, whereas per-host symbiont load and symb

295 HY5 levels increase with light intensity, which gradually enhances BIN2 activity.

296 s, use of additives, and irradiation by high light intensities with very long excitation durations, w

297 development to integrate photosynthesis and light intensity with requirements for access to water an

298 These responses could be elicited at light intensities within the physiological range and sub

299 for some weeks when activated with very low light intensity within a physiological environment.

300 target PIF3 degradation under wide ranges of light intensity without affecting the abundance of phyB.