The model couples stomatal conductance (gs) and net photosynthetic rate (PN) describing not only part of the curve up to and including saturation irradiance (Imax), but also the range above the saturation irradiance. Maximum stomatal conductance (gsmax) and Imax can be calculated by the coupled model. For winter wheat (Triticum aestivum) the fitted results showed that maximum PN
(Pmax) at 600 µmol mol-1 was more than at 350 µmol mol-1 under the same leaf temperature, which can not be explained by the stomatal closure at high CO2 concentration because gsmax at 600 µmol mol-1 was less than at 350 µmol mol-1. The irradiance-response curves for winter wheat had similar tendency, e.g. at 25 °C and 350 µmol mol-1 both PN and gs almost synchronously reached the maximum values at about 1 600 µmol m-2 s-1. At 25 °C and 600 µmol mol-1 the Imax corresponding to Pmax and
gsmax was 2 080 and 1 575 µmol m-2 s-1, respectively. and Z.-P. Ye, Q. Yu.
The calculated maximum net photosynthetic rate (PN) at saturation irradiance (I m) of 1 314.13 µmol m-2 s-1 was 25.49 µmol(CO2) m-2 s-1, and intrinsic quantum yield at zero irradiance was 0.103. The results fitted by nonrectangular hyperbolic model, rectangular hyperbolic method, binomial regression method, and the new model were compared. The maximum PN values calculated by nonrectangular hyperbolic model and rectangular hyperbolic model were higher than the measured values, and the I m calculated by nonrectangular hyperbolic model and rectangular hyperbolic model were less than measured values. Results fitted by new model showed that the response curve of PN to I was nonlinear at low I for Oryza sativa, PN increased nonlinearly with I below saturation value. Above this value, PN decreased nonlinearly with I.
Net CO2 assimilation rate (PN), stomatal conductance (gs), transpiration rate (E), and water use efficiency (WUE) in four perennial C3 species (grasses: Dactylis glomerata, Festuca rupicola, dicots: Filipendula vulgaris, Salvia nemorosa) grown for 231 d in open-top chambers at ambient (CA, 350 µmol mol-1) or elevated (CE, 700 µmol mol-1) CO2 concentrations were compared. When measured at CE, PN was significantly higher in CE plants of all four species than in the CA ones. The increase in PN was less prominent in the two grasses than in the two dicots. The E was significantly higher in the CE-grass F. rupicola and CE-dicot F. vulgaris than in the CA plants. There was no change in E owing to CE in the other grass and dicot. The gs in F. vulgaris and F. rupicola increased, while there was a decrease in D. glomerata and no change in S. nemorosa. WUE increased in all species grown in CE: four- to five-fold in the dicots and less than two-fold in the grasses. The increase in WUE was primarily due to an increase in PN and not to a decrease in E. and K. Szente, Z. Nagy, Z. Tuba.
Leaf area is one of the most important parameter for plant growth. Reliable equations were offered to predict leaf area for Zea mays L. cultivars. All equations produced for leaf area were derived as affected by leaf length and leaf width. As a result of ANOVA and multiregression analysis, it was found that there was a close relationship between actual and predicted growth parameters. The produced leaf-area prediction model in the present study is LA =
a + b L + c W + d LZ where LA is leaf area, L is leaf length, W is maximum leaf width, LZ is leaf zone and a, b, c, d are coefficients.
R2 values were between 0.88-0.97 and standard errors were found to be significant at the p<0.001 significance level. and F. Oner ... [et al.].