ライフサイエンスコーパス: photosynthetic rate

1 le alterations in partitioning that increase photosynthetic rate.

2 sol on CO(2) transport, further reducing the photosynthetic rate.

3 a-to-volume ratio, vein density, and maximum photosynthetic rate.

4 nt on the diversity and seasonal dynamics of photosynthetic rate.

5 mum leaf hydraulic capacity and thus maximum photosynthetic rate.

6 uble mutant was not linked to a reduction in photosynthetic rate.

7 for water transport in the evolution of the photosynthetic rate.

8 reases in isoprenoid end products and in the photosynthetic rate.

9 ad reduced Pi accumulation, plant growth and photosynthetic rates.

10 ates of F(soil), which were mostly driven by photosynthetic rates.

11 manipulating labeling through adjustments in photosynthetic rates.

12 nta.m(2).s(-1)), which should have decreased photosynthetic rates.

13 models to predict light-dependent growth and photosynthetic rates.

14 ll conductance is positively correlated with photosynthetic rates.

15 ency without necessarily sacrificing maximum photosynthetic rates.

16 is closely associated with CO2 diffusion and photosynthetic rates.

17 sphate supply and were associated with lower photosynthetic rates.

18 ong the only land plants to match angiosperm photosynthetic rates.

19 h depth that are consistent with patterns of photosynthetic rates.

20 Photosynthetic rates 1 and 3 d before the Rsoil measurem

21 Elevated atmospheric CO(2) enhances photosynthetic rate,(1) thereby increasing biomass produ

22 (29.74%), stomatal conductance (35.29%), and photosynthetic rate (28.79%), total phenolics (29.36%),

23 er, more numerous stomata that enable higher photosynthetic rates,(9)(,)(10)(,)(11) suggesting select

24 e measurements revealed decreases in diurnal photosynthetic rate (A') and stomatal conductance ( gs'

25 Among C(3) grasses, a high photosynthetic rate (A(area)) may depend on higher vein

26 rboxylase (V(pmaxA)) and CO(2)-saturated net photosynthetic rate (A(max)), two key parameters describ

27 d the lowest stomatal conductance (g(s)) and photosynthetic rate (A), but also maintained the highest

28 n dispute, representing such effects on leaf photosynthetic rates (A) continues to draw research atte

29 anut genotypes capable of maintaining higher photosynthetic rates (A) under stress is crucial.

30 ient CO2 diffusion into the leaf to maintain photosynthetic rates (A).

31 and an analysis of photopigment content and photosynthetic rates along boring filaments, helped us r

32 The model was extended by modeling maximum photosynthetic rate (Amax ) and light-use efficiency (Q)

33 ght-saturated stomatal conductance (gs ) and photosynthetic rate (Amax ).

34 Surprisingly, photosynthetic rates among the varieties were inversely

35 s, isoprene-emitting plants display a higher photosynthetic rate and a lower nonphotochemical quenchi

36 bivory will reinforce other factors, such as photosynthetic rate and fine-root production, impacting

37 nt plants showed a decrease in light-limited photosynthetic rate and growth, but the pigment and prot

38 Saccharum spontaneum has shown a higher net photosynthetic rate and lower soluble sugar than S. offi

39 ducing oxidative stress, resulted in reduced photosynthetic rate and nutrient availability.

40 ion, earlier snowmelt reduced soil moisture, photosynthetic rate and stomatal conductance, and increa

41 radeoff across species between plant maximum photosynthetic rate and the ability to maintain photosyn

42 s were found among cultivars and shading for photosynthetic rate and transpiration rate.

43 iar area and stomatal conductance; while net photosynthetic rate and transpiration were not affected.

44 Autotrophs from cold streams had higher photosynthetic rates and after accounting for difference

45 omol mol(-1), increased C(a) promoted higher photosynthetic rates and altered plant tissue chemistry.

46 an lead to substantial improvements in algal photosynthetic rates and biomass yield.

47 r than in mature leaves, consistent with low photosynthetic rates and delayed chloroplast development

48 however, characterized by largely unaltered photosynthetic rates and fruit yields but restricted lea

49 draulic conductivity would positively affect photosynthetic rates and growth.

50 imbing relatives, T. cordata possessed lower photosynthetic rates and leaf and stem hydraulic capacit

51 hat AGL22 expression influences steady state photosynthetic rates and lifetime water use.

52 Contrary to expectations, photosynthetic rates and mesophyll conductance both incr

53 Rubisco activation state further influencing photosynthetic rates and N-use efficiency of these criti

54 es and, specially, bryophytes had the lowest photosynthetic rates and nonstomatal diffusion conductan

55 ts of species, which are used as proxies for photosynthetic rates and nutrient and water-use efficien

56 We have now quantified the reductions of photosynthetic rates and PSI activity in the NCS6 defect

57 oncentrations and specific leaf area, faster photosynthetic rates and shorter leaf lifespan, are part

58 ckdown lines also show significantly reduced photosynthetic rates and their chloroplasts are more oxi

59 lated antenna sizes had substantially higher photosynthetic rates and two-fold greater biomass produc

60 er GS grasses (but not forbs) also had lower photosynthetic rates and water-use efficiencies.

61 dwarfism, reductions in chlorophyll levels, photosynthetic rate, and daytime carbohydrate levels, an

62 ith dynamic changes in stomatal conductance, photosynthetic rate, and photosystem II efficiency.

63 Plant height, economic yield, photosynthetic rate, and relative water content were dec

64 of leaf diffusive conductance, leaf-specific photosynthetic rate, and soil-leaf hydraulic conductance

65 le impact on leaf thickness, leaf area-based photosynthetic rates, and bundle sheath leakiness.

66 higher leaf nitrogen and phosphorus, faster photosynthetic rates, and shorter leaf life span compare

67 s, autopolyploid A. thaliana showed the same photosynthetic rate as diploids, indicating that polyplo

68 Photosynthetic rates (Asat ) were high in +4 degrees C/E

69 The maximum photosynthetic rate at 2,000 umol m(-2) s(-1) photosynth

70 e to NPQ, enabling plants to maintain a high photosynthetic rate at rising temperatures.

71 many multispecies field datasets include net photosynthetic rate at saturating irradiance and at ambi

72 leaf samples revealed that the CO2-saturated photosynthetic rate at saturating light intensities in s

73 f biomass removed because folivory may alter photosynthetic rates at a considerable distance from the

74 N and P content, leaf structure and maximum photosynthetic rates at ambient and saturating atmospher

75 The zep3 knockout strains showed reduced photosynthetic rates at higher light fluxes and reduced

76 st that ChlF can be a powerful tool to track photosynthetic rates at leaf, canopy, and ecosystem scal

77 erized as having markedly reduced growth and photosynthetic rates at saturating light, thereby constr

78 Could photosynthetic rate be increased by altered partitioning

79 hotosynthetic capacity, rather than realized photosynthetic rates being used to assess natural variat

80 f mass per area) and physiological function (photosynthetic rate, biochemical capacity and CO2 diffus

81 edicted necessary for optimization increased photosynthetic rate by 28% in potato.

82 soil CO2 efflux (FCO2 ) of sudden changes in photosynthetic rates by altering CO2 concentration in pl

83 icant reductions in predawn water potential, photosynthetic rates/capacity, and twig and needle growt

84 ovements the plants' relative water content, photosynthetic rate, chlorophyll levels, membrane stabil

85 reduced O2 inhibition of photosynthesis and photosynthetic rates comparable to those of untransforme

86 in glycolate accumulation, and reductions in photosynthetic rates compared with either single mutant.

87 lts suggest that temperature compensation of photosynthetic rates constrains the long-term temperatur

88 Photosynthetic rate correlated with trunk diameter and p

89 tosynthesis (T(optA) ) increased and maximum photosynthetic rates declined in warm-grown seedlings, b

90 found that plant height, dry weight and net photosynthetic rate decreased while leaf Na(+) concentra

91 habitats have greater MPS but higher maximum photosynthetic rates during non-water-stressed condition

92 xpression of PIF5 was sufficient to suppress photosynthetic rate, enhance response to elevated carbon

93 nd greatly enhanced stomatal conductance and photosynthetic rate, especially during late developmenta

94 Net photosynthetic rates estimated at the mean growth temper

95 xG), that produces maximum power, or maximum photosynthetic rate, for the plant system, Max(G).

96 Photosynthetic rate, however, remained high after the la

97 Diffuse radiation generally increases photosynthetic rates if total radiation is kept constant

98 thermostable RCA1 variants exhibited higher photosynthetic rates, improved development patterns, hig

99 This caused a 30% decrease in the maximum photosynthetic rate in air-adapting cells 8 h later.

100 High photosynthetic rates in A. donax resulted from a high ca

101 ) and phosphorus (P) concentrations and leaf photosynthetic rates in cone-bearing branches, branches

102 alicornia and Acanthophora spicifera, higher photosynthetic rates in G. salicornia, greater nitrogen

103 Recently, engineered increases in photosynthetic rates in other crops have been directly r

104 Using these anatomical data and measured photosynthetic rates in these C4 species, we have now ca

105 prerequisites for the evolution of enhanced photosynthetic rates in this group.

106 increased from 400 to 600 mumol mol(-1), net photosynthetic rates increased by 45 to 48% under near l

107 tion of maize (Zea mays) roots by T. virens, photosynthetic rate increases in leaves and the function

108 The best predictor of leaf level photosynthetic rate is the porosity of the leaf surface,

109 Collectively, these results suggest that photosynthetic rate largely determines mean coral delta(

110 used concomitant reductions in leaf-specific photosynthetic rate, leaf diffusive conductance, and soi

111 t have affected yield potential (single-leaf photosynthetic rate, leaf water potential).

112 ated temperature with elevated CO2, affected photosynthetic rates, leaf carbohydrates, freezing toler

113 razing pressure and significant increases in photosynthetic rates may explain the unexpected success

114 Misting of leaves had no effect on photosynthetic rate of leaves with plugs, but resulted i

115 usts increased the growth of Festuca and the photosynthetic rates of Artemisia.

116 nge have been shown to negatively affect the photosynthetic rates of boreal forest tree saplings at t

117 Photosynthetic rates of L-CO2-acclimated suppressors und

118 adiance in rice, and (b) factors controlling photosynthetic rates of leaves within the canopy.

119 However, photosynthetic rates of VL-CO2-acclimated cells under ac

120 , the large number of factors that influence photosynthetic rates often makes it difficult to measure

121 elations between peat accumulation rates and photosynthetic rates over the Northern Hemisphere.

122 in specific hydraulic conductivity and both photosynthetic rate (P = 0.080) and growth (P = 0.012).

123 Based on maximum photosynthetic rates, P. elliottii required a longer pay

124 TLA, N addition significantly enhanced leaf photosynthetic rate per area (A(area) , +12.6%), stomata

125 Their lower photosynthetic rate per leaf mass area at any given nitr

126 Similarly to other lineages, light-saturated photosynthetic rate per mass (Am ) was related negativel

127 h heat and drought tolerance through maximum photosynthetic rate per mass and leaf mass per area, res

128 In both tests, a higher photosynthetic rate per mass or per area in the favorabl

129 irst group showed higher capacity to enhance photosynthetic rates per area (Pmax), while Pmax enhance

130 s, three SO species had up to sixfold higher photosynthetic rates per photosystem II and similar or h

131 eaf light absorption, but maintained similar photosynthetic rates per unit leaf area to square wave-g

132 ments allowed these plants to maintain their photosynthetic rates per unit leaf area.

133 Clones PH 16 and PS 1319 had higher net photosynthetic rates per unit of leaf area (A), transpir

134 key physiological functions contributing to photosynthetic rate, plant productivity, and ecosystem s

135 To maintain high photosynthetic rates, plants must adapt to their light e

136 potential (psi w), transpiration rate (Tr), photosynthetic rate (Pn), and stomatal and mesophyll res

137 y reduced the leaf area, plant dry mass, net photosynthetic rate (PN), stomatal conductance (gs), int

138 s, native species had higher light-saturated photosynthetic rates, possibly as a consequence of a gre

139 lude increasing dry-season transpiration and photosynthetic rates, prolonging the life span of fine r

140 l) , inducing a decrease in leaf area before photosynthetic rate reduction.

141 e three different coatings, an inhibition of photosynthetic rate (relative electron transport rate, r

142 By altering leaf photosynthetic rates, rising [CO2] and temperature may a

143 r influences on total nitrogen accumulation, photosynthetic rate, root morphologies, and yields are n

144 We compiled data on three leaf traits (photosynthetic rate, specific leaf area, and leaf nitrog

145 trichome density, leaf water content (LWC), photosynthetic rate, stomatal conductance and intrinsic

146 al traits, including relative water content, photosynthetic rate, stomatal conductance, chlorophyll c

147 he covariation of mesophyll conductance with photosynthetic rate, stomatal conductance, water use eff

148 results link auxin biosynthesis with maximum photosynthetic rate through leaf venation and substantia

149 bohydrates (NSCs) in leaves reduces leaf net photosynthetic rate, thus internally regulating photosyn

150 adjustments in both stomatal conductance and photosynthetic rate to environmental conditions - are di

151 tments in both leaf stomatal conductance and photosynthetic rate to environmental conditions.

152 tion effects between nitrogen and shading on photosynthetic rate, transpiration rate, and total root

153 second group included functional traits, net photosynthetic rate, transpiration rate, M conductance t

154 Leaf photosynthetic rate, transpiration, plant height, leaf a

155 in leaf area occurs earlier than that in the photosynthetic rate under potassium (K) deficiency stres

156 (2) assimilation (A) have focused largely on photosynthetic rates under light-saturated steady-state

157 have evolved critical adaptations to enhance photosynthetic rates under the joint constraints of low

158 husk) substantially improved plant biomass, photosynthetic rate (up to 24.67%), stomatal conductance

159 o reduce the impacts of drought and increase photosynthetic rates via two key mechanisms: first, thro

160 The net photosynthetic rate was almost 50% slower in O. sativa a

161 horus and iron, but unlike angiosperms, leaf photosynthetic rate was not associated with leaf hydraul

162 on (g(s)), and the g(m)/g(s) ratio.While net photosynthetic rate was positively correlated with gm, n

163 e individual with the higher light-saturated photosynthetic rate was selected and used to seed the ne

164 dry weight, SPAD chlorophyll meter reading, photosynthetic rate, water use efficiency, number of nod

165 nodule activity, and in situ canopy apparent photosynthetic rate were measured in stressed and nonstr

166 Declining host photosynthetic rates were also significantly inversely c

167 ue fractions of reproductive branches, where photosynthetic rates were reduced.

168 Photosynthetic rates were similar between strains, altho

169 All crops suffer declines in photosynthetic rate when temperatures cross critical thr

170 ated with higher stomatal conductance, lower photosynthetic rate (when CO2 supply is factored out), a

171 aulic conductance, stomatal conductance, and photosynthetic rate, whereas palmately veined leaves wer

172 How consequent alterations in photosynthetic rates will impact fluxes in photosyntheti

173 Higher leaf photosynthetic rate, WUE, and lower stomatal conductance

174 sults occasionally show increased leaf-level photosynthetic rates, WUE, LAI, and plant growth under e