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1 uble mutant was not linked to a reduction in photosynthetic rate.
2 for water transport in the evolution of the photosynthetic rate.
3 nt on the diversity and seasonal dynamics of photosynthetic rate.
4 reases in isoprenoid end products and in the photosynthetic rate.
5 le alterations in partitioning that increase photosynthetic rate.
6 mum leaf hydraulic capacity and thus maximum photosynthetic rate.
7 ll conductance is positively correlated with photosynthetic rates.
8 ency without necessarily sacrificing maximum photosynthetic rates.
9 sphate supply and were associated with lower photosynthetic rates.
10 is closely associated with CO2 diffusion and photosynthetic rates.
11 h depth that are consistent with patterns of photosynthetic rates.
14 and an analysis of photopigment content and photosynthetic rates along boring filaments, helped us r
15 The model was extended by modeling maximum photosynthetic rate (Amax ) and light-use efficiency (Q)
18 bivory will reinforce other factors, such as photosynthetic rate and fine-root production, impacting
19 nt plants showed a decrease in light-limited photosynthetic rate and growth, but the pigment and prot
20 radeoff across species between plant maximum photosynthetic rate and the ability to maintain photosyn
22 iar area and stomatal conductance; while net photosynthetic rate and transpiration were not affected.
24 omol mol(-1), increased C(a) promoted higher photosynthetic rates and altered plant tissue chemistry.
25 r than in mature leaves, consistent with low photosynthetic rates and delayed chloroplast development
26 however, characterized by largely unaltered photosynthetic rates and fruit yields but restricted lea
28 imbing relatives, T. cordata possessed lower photosynthetic rates and leaf and stem hydraulic capacit
31 Rubisco activation state further influencing photosynthetic rates and N-use efficiency of these criti
32 ts of species, which are used as proxies for photosynthetic rates and nutrient and water-use efficien
33 We have now quantified the reductions of photosynthetic rates and PSI activity in the NCS6 defect
34 dwarfism, reductions in chlorophyll levels, photosynthetic rate, and daytime carbohydrate levels, an
36 of leaf diffusive conductance, leaf-specific photosynthetic rate, and soil-leaf hydraulic conductance
37 s, autopolyploid A. thaliana showed the same photosynthetic rate as diploids, indicating that polyplo
39 many multispecies field datasets include net photosynthetic rate at saturating irradiance and at ambi
40 leaf samples revealed that the CO2-saturated photosynthetic rate at saturating light intensities in s
41 f biomass removed because folivory may alter photosynthetic rates at a considerable distance from the
42 N and P content, leaf structure and maximum photosynthetic rates at ambient and saturating atmospher
43 st that ChlF can be a powerful tool to track photosynthetic rates at leaf, canopy, and ecosystem scal
44 erized as having markedly reduced growth and photosynthetic rates at saturating light, thereby constr
46 f mass per area) and physiological function (photosynthetic rate, biochemical capacity and CO2 diffus
47 soil CO2 efflux (FCO2 ) of sudden changes in photosynthetic rates by altering CO2 concentration in pl
48 reduced O2 inhibition of photosynthesis and photosynthetic rates comparable to those of untransforme
49 in glycolate accumulation, and reductions in photosynthetic rates compared with either single mutant.
50 lts suggest that temperature compensation of photosynthetic rates constrains the long-term temperatur
51 xpression of PIF5 was sufficient to suppress photosynthetic rate, enhance response to elevated carbon
52 nd greatly enhanced stomatal conductance and photosynthetic rate, especially during late developmenta
54 thermostable RCA1 variants exhibited higher photosynthetic rates, improved development patterns, hig
57 ) and phosphorus (P) concentrations and leaf photosynthetic rates in cone-bearing branches, branches
58 Using these anatomical data and measured photosynthetic rates in these C4 species, we have now ca
59 increased from 400 to 600 mumol mol(-1), net photosynthetic rates increased by 45 to 48% under near l
60 tion of maize (Zea mays) roots by T. virens, photosynthetic rate increases in leaves and the function
61 used concomitant reductions in leaf-specific photosynthetic rate, leaf diffusive conductance, and soi
63 ated temperature with elevated CO2, affected photosynthetic rates, leaf carbohydrates, freezing toler
64 razing pressure and significant increases in photosynthetic rates may explain the unexpected success
66 nge have been shown to negatively affect the photosynthetic rates of boreal forest tree saplings at t
71 in specific hydraulic conductivity and both photosynthetic rate (P = 0.080) and growth (P = 0.012).
73 Similarly to other lineages, light-saturated photosynthetic rate per mass (Am ) was related negativel
75 irst group showed higher capacity to enhance photosynthetic rates per area (Pmax), while Pmax enhance
76 eaf light absorption, but maintained similar photosynthetic rates per unit leaf area to square wave-g
78 key physiological functions contributing to photosynthetic rate, plant productivity, and ecosystem s
80 potential (psi w), transpiration rate (Tr), photosynthetic rate (Pn), and stomatal and mesophyll res
81 y reduced the leaf area, plant dry mass, net photosynthetic rate (PN), stomatal conductance (gs), int
82 s, native species had higher light-saturated photosynthetic rates, possibly as a consequence of a gre
83 lude increasing dry-season transpiration and photosynthetic rates, prolonging the life span of fine r
84 e three different coatings, an inhibition of photosynthetic rate (relative electron transport rate, r
86 r influences on total nitrogen accumulation, photosynthetic rate, root morphologies, and yields are n
87 he covariation of mesophyll conductance with photosynthetic rate, stomatal conductance, water use eff
88 results link auxin biosynthesis with maximum photosynthetic rate through leaf venation and substantia
89 tion effects between nitrogen and shading on photosynthetic rate, transpiration rate, and total root
90 second group included functional traits, net photosynthetic rate, transpiration rate, M conductance t
92 o reduce the impacts of drought and increase photosynthetic rates via two key mechanisms: first, thro
94 horus and iron, but unlike angiosperms, leaf photosynthetic rate was not associated with leaf hydraul
95 on (g(s)), and the g(m)/g(s) ratio.While net photosynthetic rate was positively correlated with gm, n
96 e individual with the higher light-saturated photosynthetic rate was selected and used to seed the ne
97 nodule activity, and in situ canopy apparent photosynthetic rate were measured in stressed and nonstr
101 ated with higher stomatal conductance, lower photosynthetic rate (when CO2 supply is factored out), a
102 aulic conductance, stomatal conductance, and photosynthetic rate, whereas palmately veined leaves wer
103 sults occasionally show increased leaf-level photosynthetic rates, WUE, LAI, and plant growth under e
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