The genetic variation in low temperature sensitivity of eight tomato genotypes grown at suboptimal temperature (19 °C) and at low irradiance (140 pmol m'2 s**) was assessed at the plant, chloroplast and thylakoid membrane levels. Temperature effects on the thylakoid membrane were determined by measuring the maximum fluorescence (Fp) and the maximal fluorescence rise (ADP) of induction traces of leaf discs at decreasing temperatures (30, 28, ... 0 °C). Two discontinuities were found in Fp versus temperature curves: a low temperature break at ca. 12 °C (LTB) and a high temperature break at ca. 22 °C (FITB). Below LTB, sFp and sDP were determined as the temperature induced changes in Fp, respectively ADP. Chloroplast functioning was determined by measuring net CO2 fixation rate (E^) of leaves. Plant performance was determined by measuring the increase in leaf area and sho ot dry mass in time. Correlations between the various parameters were analysed across the genotypic variation found. Chlorophyll (Chl) fluorescence parameters were not correlated with plant performance at suboptimal growth conditions. of leaves was correlated with plant performance, but only at ambient CO2. Effects of stomatal resistance on were large. The Chl fluorescence parameters LTB, sFp and sDP could distinguish between tomato genotypes. Nevertheless, the ranking of the genotypes depended on the specific parameter selected, indicating that each parameter assessed a different aspect of the heterogeneous temperature dependence of Chl fluorescence induction. Their genetic variation suggested that the genotypes differed in the organisation and fimctioning of the thylakoid membrane. These differences were not reflected in of leaves or plant performance.
Seedlings of Bidens cernua L. emerged when mean air temperature was 17.0±1.3 °C. The highest net photosynthetic rate (PN), 13.8±0.8 µmol(CO2) m-2 s-1, was monitored during the vegetative period (May-August), decreasing on an average by 50 % during flowering (August-September) and during fruiting (September-November) phases. The senescence phase (October-November) was characterised by 79, 58, and 18 % decrease of PN, chlorophyll content, and leaf area (LA), respectively, from the maximum values. The time span from seedling emergence to the end of fruiting phase was 202 d. The total plant biomass was 1.58±0.05 g of which 81 % was aboveground plant portion. The total dry mass relative growth rate averaged over the assimilation period was 0.0804±0.0002 kg kg-1 d-1, and it was correlated to both the net assimilation rate (NAR) and the leaf area ratio (LAR). and L. Gratani ... [et al.].