Photosynthetic light and temperature response curves were measured seasonally in seedlings of white spruce (Picea glauca (Moench.) Voss) grown for two years in the understory of aspen (Populus tremuloides Michx.) or in the open in central Alberta. Light-saturated rate of net photosynthesis, the optimum temperature for net photosynthesis, transpiration rate, photochemical efficiency, and stomata...

We investigated whether leaf dark respiration (nonphotorespiratory mitochondrial CO2 release) is inhibited by light in several Poa species, and whether differences in light inhibition between the species are related to differences in the rate of leaf net photosynthesis. Four lowland (Poa annua L., Poa compressa L., Poa pratensis L., and Poa trivialis L.), one subalpine (Poa alpina L.), and two ...

The hypothesis that net photosynthesis is diminished in many plant species because of a high rate of CO(2) evolution in the light has been tested further. High rates of CO(2) output in CO(2)-free air in comparison with dark respiration were found in Chlamydomonas reinhardi, wheat leaves, tomato leaves, and to a lesser extent in Chlorella pyrenoidosa by means of the (14)C-photorespiration assay....

Sugar beets (Beta vulgaris L.) infected with the Beet Yellows Virus exhibit lower rates of net photosynthesis at light saturation than do healthy plants. These Pn reductions were correlated with increases in leaf resistance to water vapor loss. Theoretical analyses demonstrated that, although the leaf resistance to water vapor loss increases could account for a major part of the net photosynthe...

Effects of moderate heat on growth and photosynthesis were investigated in two clonal genotypes of Acer rubrum L., originally collected from the thermally contrasting habitats of Florida and Minnesota, USA, and known in the horticultural trade for sensitivity and insensitivity to heat, respectively. Under both common garden and warm greenhouse conditions (day/night temperature of 33/25 degrees ...

Net photosynthetic rates of developing foliage and one-year-old foliage of loblolly pine (Pinus taeda L.) were measured under field conditions. In the subsequent year, net photosynthesis and dark respiration rates of current-year and one-year-old foliage were measured under controlled environmental conditions. Loblolly pine foliage grows slowly, reaching its final size 3.5 to 4 months after bud...

Responses of photosynthesis to carbon dioxide (CO2) partial pressure and irradiance were measured on leaves of 39-year-old trees of manuka (Leptospermum scoparium J. R. Forst. & G. Forst.) and kanuka (Kunzea ericoides var. ericoides (A. Rich.) J. Thompson) at a field site, and on leaves of young trees grown at three nitrogen supply rates in a nursery, to determine values for parameters in a mod...

Radiation use efficiency (RUE) provides a useful diagnostic approach for estimating carbon accumulation by terrestrial plant communities. A model for instantaneous gross photosynthesis by a canopy, considering sunlit and shaded leaves, variation of maximum rate of leaf photosynthesis within the canopy and a solution of the radiative transfer equation for propagation of direct and diffuse photos...

The combined effect of selenium (Se) foliar spraying and drought was studied for 3 months in two cultivars of potato; Bard and Adora in Ljubljana, Slovenia. Four combinations of treatments were conducted: well-watered plants with and without Se foliar spraying, and drought exposed plants with and without Se foliar spraying. Net photosynthesis, transpiration rate, quantum yield of photosystem II...

The rate of dark CO(2) efflux from mature wheat (Triticum aestivum cv Gabo) leaves at the end of the night is less than that found after a period of photosynthesis. After photosynthesis, the dark CO(2) efflux shows complex dependence on time and temperature. For about 30 minutes after darkening, CO(2) efflux includes a large component which can be abolished by transferring illuminated leaves to...