Hypothesis: For any one time and place a 'functional signature' can be derived for a sample of herbaceous vegetation in a way that concisely represents the balance between the different clusters of functional attributes that are present among component species. Methods: We developed a spreadsheet-based tool for calculating functional signatures within the context of the C-S-R system of plant functional types. We used the tool to calculate and compare signatures for specimen British vegetation samples which differed in management regime and location in time. Conclusion:The integrative power of the 'C-S-R signature' is useful in comparative studies involving widely differing samples. Movements in the signature can be used to indicate degree of resistance, resilience, eutrophication and dereliction. Systems of plant functional types other than C-S-R might also be approached in this way. Availability: The tool can be downloaded free of charge from the first author's web pages or from the journal's electronic archive.
Hypothesis: For any one time and place a ‘functional signature’ can be derived for a sample of herbaceous vegetation in a way that concisely represents the balance between the different clusters of functional attributes that are present among component species. Methods: We developed a spreadsheet‐based tool for calculating functional signatures within the context of the C‐S‐R system of plant functional types. We used the tool to calculate and compare signatures for specimen British vegetation samples which differed in management regime and location in time. Conclusion: The integrative power of the ‘C‐S‐R signature’ is useful in comparative studies involving widely differing samples. Movements in the signature can be used to indicate degree of resistance, resilience, eutrophication and dereliction. Systems of plant functional types other than C‐S‐R might also be approached in this way. Availability: The tool can be downloaded free of charge from the first author's web pages or from the journal's electronic archive.
The sensitivity of seminatural grasslands to ozone (O 3 ) pollution is not well known, in spite of the important function of these common ecosystems for agriculture and nature conservation. A 5-year field experiment was carried out at a rural, mid-elevation site at Le Mouret (Switzerland) to investigate the effect of elevated O 3 on yield and species composition of a permanent, extensively managed, species-rich old pasture. Using a free-air fumigation system, circular plots of 7 m diameter were exposed to either ambient air (control plots) or to air containing O 3 of approximately 1.5 Â ambient concentrations. The resulting accumulated O 3 exposure over the threshold of 40 ppb for one season ranged from 13.3 to 59.5 ppm h in the elevated O 3 plots, and from 1.0 to 20.7 ppm h in the control plots. Subplots in each ring were harvested three times each year, and harvested biomass was separated into functional groups (FGs) (grasses, legumes, forbs). Productivity in both treatments decreased over time, but the yield of O 3 -exposed plots decreased faster than that of the control plots, with the reduction being twice as large by the end of the fifth season. Compared with the ambient air control, loss in annual dry matter yield was 23% after 5 years. The change in annual biomass production because of O 3 stress was accompanied by a change in the fractions of FGs, with the legume fraction showing a strong negative response. Such long-term effects of O 3 stress could have negative implications for the maintenance of biological diversity in rural landscapes across large areas of Europe. The results from this first long-term experiment show that a moderately elevated O 3 level reduces the productivity of intact grasslands during a 5-year exposure under real field conditions.
A range of plant species typical of semi-natural grasslands were tested for their sensitivity to short-term ozone injury under normal and reduced irrigation, and in relationship to air vapour pressure deficit. Potted specimens of 24 herbs, legumes and grasses were exposed during two seasons to four O$ treatments in open-top chambers. The ozone treatments were : (a) charcoal-filtered air ; (b) charcoal-filtered air plus ozone to match ambient levels ; (c) charcoal-filtered air plus O $ to ambient levels 1n5 and (d ) charcoal-filtered air with ozone added to twice ambient levels during selected episodes of 7-13 d. During these ozone episodes, half of the plants in each ozone treatment received reduced irrigation (dry treatment) while the rest was kept under full irrigation (wet treatment). Type and date of first occurrence of leaf injury were noted during individual growth periods. Plants were harvested three times per year, and the percentage of injured leaves was recorded. Depending on species, injury symptoms were expressed as flecking (O $ -specific injury), leaf yellowing or anthocyanin formation. Carum carvi and most species of the Fabaceae family (Onobrychis sativa, Trifolium repens, Trifolium pratense) were found to be most responsive to O $ , injury occurring after only a few days of exposure in treatment (b). An episodic reduction in irrigation tended to reduce the expression of O $ -specific symptoms, but only in species for which a reduction in soil moisture potential and an associated reduction in stomatal conductance during the dry episodes were observed. In other species, the protection from O $ injury seemed to be of little importance. Using artificial neural networks the injury response of nine species was analysed in relation to Species, stomatal conductance, ozone as AOT40 (accumulated exposure above a threshold of 0n04 ppm for periods with global radiation 50 W m −# (Fuhrer et al., 1997)), mean relative growth rate, air vapour pressure deficit and global radiation. In the model with all factors, Species was most important, and when Species was omitted, stomatal conductance was the most important determinant for leaf injury to occur, whereas mean relative growth rate was less important. With no plant-related factors included, air vapour pressure deficit and AOT40 were of highest importance. Only in eight species was a positive relationship found between these two factors during the five days before the onset of injury, indicating increasing protection from ozone with increasing air vapour pressure deficit in some but not all species. These data show that across a range of grassland species, leaf injury caused by elevated levels of ozone is most likely to occur in species with high stomatal conductance and that protection from ozone during dry periods is species-specific and depends on a reduction in stomatal conductance due to a decrease in soil moisture potential. Protection under increased vapour pressure deficit can occur in some but not all species, depending on the relationship between stom...
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