Summary.The structural characteristics of a diverse array of Quercus coccifera canopies were assessed and related to measured and computed light attenuation, proportion of sunlit foliage, foliage temperatures, and photosynthesis and diffusive conductance behavior in different canopy layers. A canopy model incorporating all components of shortwave and longwave radiation, and the energy balance, conductance, and CO 2 and H20 exchanges of all leaf layers was developed and compared with measurements of microclimate and gas exchange in canopies in four seasons of the year. In the denser canopies with a leaf area index (LAI) greater than 5, there is little sunlit foliage and the diffuse radiation (400-700 nm) is attenuated to 5% or less of the global radiation (400-700 nm) incident on the top of the canopy. Foliage of this species is nonrandomly distributed with respect to azimuth angle, and within each canopy layer, foliage azimuth and inclination angles are correlated. A detailed version of the model which computed radiation interception and photosynthetic light harvesting according to these nonrandom distributions indicated little difference in whole-canopy gas exchange from calculations of the normal model, which assumes random azimuth orientation. The contributions of different leaf layers to canopy gas exchange are not only a function of the can- opy microclimate, but also the degree to which leaves in the lower layers of the canopy exhibit more shade-leaf characteristics, such as low photosynthetic and respiratory capacity and maximal conductance. On cloudless days, the majority of the foliage in a canopy of 5.4 LAI is shaded -70%-90% depending on the time of year. Yet, the shaded foliage under these conditions is calculated to contribute only about one-third of the canopy carbon gain. This contribution is about the same as that of the upper 13% of the canopy foliage. Computed annual whole-canopy carbon gain and water use are, respectively, 60% and 100% greater for a canopy of 5 LAI than for one of 2 LAI. Canopy water-use efficiency is correspondingly less for the canopy of 5 LAI than for that of 2 LAI, but most of this difference is apparent during the cool months of the year, when moisture is more abundant.

We used a partial diallel mating design to examine morphologic response to supplementary ultraviolet-B (UV-B) radiation of seven ecotypes of Arabidopsis thaliana L. Heynh. from several geographic locations in Europe. We were particularly interested in the inheritance of UV-B tolerance by the F1 generation. Morphologic traits included plant height, rosette diameter, number of shoots (lateral branches from the rosette) and branches (lateral branches above the rosette), and reproductive and vegetative dry mass. To effect a large difference in UV treatments, plants under treatment received 11 kJ/m2/day of biologically effective UV-B radiation while control plants received no UV-B radiation. Genotype effects were observed for all traits (P < .0001), but a significant treatment effect and genotype x treatment interactions were detected only for plant height (P = .0001), rosette diameter (P = .0229), and vegetative (P = .0260) and reproductive dry mass (P = .0900). General combining ability was significant for plant height (P < .0001) and vegetative mass (P = .0563), whereas specific combining ability was significant for rosette diameter (P = .0220) and vegetative mass (P = .0506). These results suggest that both pure lines and hybrids of Arabidopsis can be developed for greater tolerance of UV-B radiation. Similar findings for crop species might lead to the development of UV tolerant varieties.

Nitrate uptake in pot-grown, well watered and water-stressed Artemisia tridentata seedlings was determined both during drought and during recovery from drought using 1 5~0 5 .Water deficit caused a 40% decrease in NO? uptake compared to well watered plants and the restricted NO? uptake persisted 4 days after rewatering. Between 4 and 14 days after rewatering, NOS uptake in previously stressed plants was the same as that of the controls. Root relative growth rate (RGR) during the drying cycle was about one-fourth that of the control, but recovered to the control level within 4 days after rewatering. Between 4 and 14 days after rewatering, the previously droughted plant roots exhibited nearly three times greater RGR than the control plant roots. Estimates of root solute content indicated that at no time during the stress and recovery periods did the droughted roots exhibit osmotic adjustment. Changes in root growth properties were uncoupled from turgor. During the recovery period, drought-induced adjustments in cell wall yielding properties are thought to have increased root growth in previously stressed seedlings. Nevertheless, the greater root growth of previously droughted plants did not result in more NO? acquisition than in control plants. The pattern of NO? uptake upon rewatering was apparently more closely associated with root uptake capacity.

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