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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.
12                                              Photosynthetic rates 1 and 3 d before the Rsoil measurem
13 ient CO2 diffusion into the leaf to maintain photosynthetic rates (A).
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)
16 ght-saturated stomatal conductance (gs ) and photosynthetic rate (Amax ).
17                                Surprisingly, photosynthetic rates among the varieties were inversely
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
21 s were found among cultivars and shading for photosynthetic rate and transpiration rate.
22 iar area and stomatal conductance; while net photosynthetic rate and transpiration were not affected.
23      Autotrophs from cold streams had higher photosynthetic rates and after accounting for difference
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
27 draulic conductivity would positively affect photosynthetic rates and growth.
28 imbing relatives, T. cordata possessed lower photosynthetic rates and leaf and stem hydraulic capacit
29 hat AGL22 expression influences steady state photosynthetic rates and lifetime water use.
30                    Contrary to expectations, photosynthetic rates and mesophyll conductance both incr
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
35 ith dynamic changes in stomatal conductance, photosynthetic rate, and photosystem II efficiency.
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
38                                              Photosynthetic rates (Asat ) were high in +4 degrees C/E
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
45                                        Could photosynthetic rate be increased by altered partitioning
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
53 xG), that produces maximum power, or maximum photosynthetic rate, for the plant system, Max(G).
54  thermostable RCA1 variants exhibited higher photosynthetic rates, improved development patterns, hig
55    This caused a 30% decrease in the maximum photosynthetic rate in air-adapting cells 8 h later.
56                                         High photosynthetic rates in A. donax resulted from a high ca
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
62 t have affected yield potential (single-leaf photosynthetic rate, leaf water potential).
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
65           Misting of leaves had no effect on photosynthetic rate of leaves with plugs, but resulted i
66 nge have been shown to negatively affect the photosynthetic rates of boreal forest tree saplings at t
67                                              Photosynthetic rates of L-CO2-acclimated suppressors und
68 adiance in rice, and (b) factors controlling photosynthetic rates of leaves within the canopy.
69                                     However, photosynthetic rates of VL-CO2-acclimated cells under ac
70 elations between peat accumulation rates and photosynthetic rates over the Northern Hemisphere.
71  in specific hydraulic conductivity and both photosynthetic rate (P = 0.080) and growth (P = 0.012).
72                             Based on maximum photosynthetic rates, P. elliottii required a longer pay
73 Similarly to other lineages, light-saturated photosynthetic rate per mass (Am ) was related negativel
74                      In both tests, a higher photosynthetic rate per mass or per area in the favorabl
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
77 ments allowed these plants to maintain their photosynthetic rates per unit leaf area.
78  key physiological functions contributing to photosynthetic rate, plant productivity, and ecosystem s
79                             To maintain high photosynthetic rates, plants must adapt to their light e
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
85                             By altering leaf photosynthetic rates, rising [CO2] and temperature may a
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
91                                         Leaf photosynthetic rate, transpiration, plant height, leaf a
92 o reduce the impacts of drought and increase photosynthetic rates via two key mechanisms: first, thro
93                                      The net photosynthetic rate was almost 50% slower in O. sativa a
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
98                               Declining host photosynthetic rates were also significantly inversely c
99 ue fractions of reproductive branches, where photosynthetic rates were reduced.
100                                              Photosynthetic rates were similar between strains, altho
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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