ALBERT

Notes: [Auszug] We have investigated first, the possibility that genetic differences between local populations of A. confertifolia and E. lanata explain their distribution in or near the five com munities within the Atriplex-Eurotia zone. Second, we investi gated the contribution of genetic differences to the wide ...

Notes: Soybean [Glycine max (L.) Merr.] cultivar Essex was grown and tested for sensitivity to UV-B radiation (280–320 nm) under different combinations of UV-A (320–400 nm) and PFD (400–700 nm) radiation in four simultaneous field experiments. The radiation conditions were effected with combinations of filtered solar radiation and UV-B and UV-A lamps electronically modulated to track ambient radiation. Significant UV-B-caused decreases in total aboveground production and growth were seen only when PFD and UV-A were reduced to less than half their flux in sunlight. When PFD was low, UV-A appeared to be particularly effective in mitigating UV-B damage. However, when PFD was high, substantial UV-A did not appear to be required for UV-B damage mitigation. Leaf chlorophyll fluorescence did not indicate photosynthetic damage under any radiation combination. With UV-B, leaves in all experiments exhibited increased UV-absorbing pigments and decreased whole-leaf UV transmittance. Results of these field experiments indicate difficulties in extrapolating from UV-B experiments conducted in glasshouse or growth cabinet conditions to plant UV-B sensitivity in the field. Implications for UV radiation weighting functions in evaluating atmospheric ozone reduction are also raised.

Notes: The ecosystems of Tierra del Fuego (in southern Patagonia, Argentina) are seasonally exposed to elevated levels of ultraviolet-B radiation (UV-B: 280–315 nm), due to the passage of the ‘ozone hole’ over this region. In the experiments reported in this article the effects of solar UV-B and UV-A (315–400 nm) on two UV-B defence-related processes: the accumulation of protective UV-absorbing compounds and DNA repair, were tested. It was found that the accumulation of UV-absorbing sunscreens in Gunnera magellanica leaves was not affected by plant exposure to ambient UV radiation. Photorepair was the predominant mechanism of cyclobutane-pyrimidine dimer (CPD) removal in G. magellanica. Plants exposed to solar UV had higher CPD repair capacity under optimal conditions of temperature (25 °C) than plants grown under attenuated UV. There was no measurable repair at 8 °C. The rates of CPD repair in G. magellanica plants were modest in comparison with other species and, under equivalent conditions, were about 50% lower than the repair rates of Arabidopsis thaliana (Ler ecotype). Collectively our results suggest that the susceptibility of G. magellanica plants to current ambient levels of solar UV-B in southern Patagonia may be related to a low DNA repair capacity.

Notes: [Auszug] We conducted two field experiments with Artemisia tridentata ssp. vaseyana (Rydb.) Beetle, a dominant shrub in western North America. One experiment was with a co-occurring grass, Agropyron spicatum (Pursh) Scribn. and Smith, and one with Agropyron desertorum (Fisch. ex Link) Schult., a grass from ...

Notes: Summary The effects of the spatial pattern of defoliation within a tussock grass, Agropyron desertorum, were investigated at a semiarid field site. In the middle of the spring growing season (mid-May), tussocks were clipped in repeatable defoliation patterns, and the regrowth of foliage was monitored. These clipping patterns involved removal of foliage from different locations within the tussock, but the total amount of foliage removed was held constant. Active meristems were left intact in all cases. The spatial pattern of defoliation affected both initial rates of tussock regrowth and total growing-season aboveground biomass production. When leaves were removed low in the tussock (older leaves), regrowth was greater than after removal of the same quantity of foliage high in the canopy (younger leaves). These differences in regrowth were due to differences in the rate of new tissue production rather than differences in the timing of senescence. The results were consistent over two years even though aboveground production differed considerably between years. The interaction of the spatial pattern and timing of defoliation was also studied by clipping additional plants in late May. The timing of defoliation affected the relative influence of different defoliation patterns on regrowth. In those defoliation patterns where active meristems were not removed in the late-May clipping, there were no differences in regrowth of tussocks which had either upper or lower foliage removed. However, because the grass culms had elongated by late May, active meristems were higher and were removed by one of the defoliation pattern treatments (a uniform clipping). This resulted in much less regrowth. Differences in the effects of clipping patterns applied in late May were associated with this removal of active meristems. Whereas, differences among clipping treatments following the earlier mid-May defoliation were probably a result of changes in factors which affected tussock carbon gain (e.g., light interception, foliage age structure). In either case, the spatial pattern of defoliation within a tussock grass clearly had significant effects on aboveground regrowth.

Notes: Summary The spatial pattern of foliage removal from a tussock grass can influence regrowth through effects on daily carbon gain (CERd). This field study examined the extent to which tussock photosynthetic responses to different defoliation patterns were associated with changes in whole-canopy attributes (e.g., foliage age structure, canopy light microclimate). During the spring growing season, 60% of the green foliage area was removed from individual Agropyron desertorum tussocks with scissors in different spatial patterns. These patterns represented extremes of defoliation patterns that might be inflicted by natural herbivores. Tussock photosynthesis (per unit foliage area) at high light (2000 μmol photons m−2 s−1 between 400 and 700 nm; P2000) increased following clipping with all defoliation patterns. The increases in P2000 were greater when leaves were removed from low in the tussock (older leaves) than if leaves high in the canopy (younger leaves) were removed. These relative changes of P2000 among clipping patterns paralleled the responses of CERd and regrowth from an earlier study. Furthermore, the changes in P2000 corresponded with increases in the proportion of foliage within the tussocks that was directly illuminated at midday. The greater photosynthesis of tussocks after lower-leaf removal was directly related to a higher proportion of younger foliage and a smaller fraction of foliage shaded within the tussock. In a dense canopy, such as these grass tussocks, the influence of defoliation on whole-canopy attributes may be of primary importance to whole-plant photosynthetic responses.

Notes: Summary Agropyron desertorum, a grazing-tolerant bunchgrass introduced to the western U.S. from Eurasia, and Agropyron spicatum, a grazing-sensitive bunchgrass native to North America, were examined in the field for photosynthetic capacity, growth, resource allocation, and tiller dynamics. These observations allowed identification of physiological characteristics that may contribute to grazing tolerance in semiarid environments. A uniform matrix of sagebrush, Artemisia tridentata, provided an ecologically relevant competitive environment for both bunch-grass species. Physiological activity, growth, and allocation were also followed during recovery from a severe defoliation treatment and were correlated with tiller dynamics. Potential photosynthetic carbon uptake of both species was dominated by stems and leaf sheaths during June, when maximum uptake rates occurred. For both species, water use efficiency of stems and sheaths was similar to that of leaf blades, but nitrogen investment per photosynthetic surface area was less than in blades. In addition, soluble carbohydrates in stems and sheaths of both species constituted the major labile carbon pools in control plants. Contrary to current theory, these findings suggest that culms from which leaf blades have been removed should be of considerable value to defoliated bunchgrasses, and in the case of partial defoliation could provide important supplies of organic nutrients for regrowth. These interpretations, based on total pool sizes, differ markedly from previous interpretations based on carbohydrate concentrations alone, which suggested that crowns contain large carbohydrate reserves. In this study, crowns of both species contained a minor component of the total plant carbohydrate pool. Following defoliation, A. desertorum plants rapidly reestablished a canopy with 3 to 5 times the photosynthetic surface of A. spicatum plants. This difference was primarily due to the greater number of quickly growing new tillers produced following defoliation. Agropyron spicatum produced few new tillers following defoliation despite adequate moisture, and carbohydrate pools that were equivalent to those in A. desertorum. Leaf blades of regrowing tillers had higher photosynthetic capacity than blades on unclipped plants of both species, but the relative increase, considered on a unit mass, area, or nitrogen basis, was greater for A. desertorum than for A. spicatum. Agropyron desertorum also had lower investment of nitrogen and biomass per unit area of photosynthetic tissues, more tillers and leaves per bunch, and shorter lived stems, all of which can contribute to greater tolerance of partial defoliation. Greater flexibility of resource allocation following defoliation was demonstrated by A. desertorum for both nitrogen and carbohydrates. Relatively more allocation to the shoot system and curtailed root growth in A. desertorum resulted in more rapid approach to the preclipping balance between the root and shoot systems, whereas root growth in A. spicatum continued unabated following defoliation. Nitrogen required for regrowth in both species was apparently supplied by uptake rather than reserve depletion. Carbohydrate pools in the shoot system of both species remained very low following severe defoliation and were approximately equivalent to carbon fixed in one day by photosynthesis of the whole canopy.

Notes: Summary The bunchgrass growth form, which is very prominent in water-limited environments, can result in considerable self-shading of photosynthetically active foliage. The consequences of this growth form for light interception and water-use efficiency (photosynthesis/transpiration, P/T) were investigated for two Agropyron species which differ in tussock density and degree of self-shading. During the period of most active gas exchange, the tussocks were very compact and photosynthesis of shaded foliage was markedly light-limited. Stomatal control of older shaded foliage was poorly attuned for water-use efficiency. At low light, P/T decreased and intercellular CO2 concentrations increased. Despite differences in architecture and amount of shaded foliage, P/T of whole tussocks under ambient field conditions did not differ between these species. Partial defoliation decreased, rather than increased, P/T, primarily as a result of the poor photosynthetic light harvesting by the remaining foliage. Despite self-shading, the architecture of widely-spaced bunchgrasses provides for interception of as much direct beam solar radiation as is calculated for a rhizomatous grass occupying an area six-fold greater than the ground area underneath the canopy of these bunchgrasses.

Notes: Summary An automated, fiber optic point quadrat system for vegetation sampling is described. Because the effective point diameter of this system never exceeds 25 μm it minimizes the substantial errors which can arise with conventional point quadrats. Automatic contact detection eliminates operator subjectivity, and permits work in dense canopies. Additionally, sampling speed is increased over that of conventional systems.