Photosynthetic stimulation and stomatal conductance (Gs) depression in Quercus ilex leaves at a CO2 spring suggested no down-regulation. The insensitivity of Gs to a CO2 increase (from ambient 1500 to 2000 μmol mol-1) suggested stomatal acclimation. Both responses are likely adaptations to the special environment of CO2 springs. At the CO2-enriched site, not at the control site, photosynthesis decreased 9% in leaves exposed to 2x ambient O3 concentrations in branch enclosures, compared to controls in charcoal-filtered air. The stomatal density reduction at high CO2 was one-third lower than the concomitant Gs reduction, so that the O3 uptake per single stoma was lower than at ambient CO2. No significant variation in monoterpene emission was measured. Higher trichome and mesophyll density were recorded at the CO2-enriched site, accounting for lower O3 sensitivity. A long-term exposure to H2S, reflected by higher foliar S-content, and CO2 might depress the antioxidant capacity of leaves close to the vent and increase their O3 sensitivity. Very high CO2 concentrations did not compensate for the effects of O3 on holm oak photosynthesis.

The level II approach of the critical loads concept adopted by the UNECE aims at a flux based evaluation and takes into account environmental factors governing stomatal conductance. These factors will probably be affected by global change. The flux concept predicts that a decrease in stomatal conductance would protect trees from air pollution effects by decreasing uptake. However, experimental evidence is inconclusive. Numerous results suggest that pollutants and factors subject to global change (drought, CO2) may interact and even exacerbate effects, probably because antioxidative defense systems are involved in both, defense against pollutant effects and protection from natural stress. An effective pollutant dose, which is weighted by physiological defense capacity, would better predict such effects. In this review paper we argue that the flux-based approach is imperfect, because global change effects may also modify the physiological susceptibility to ozone. Instead, a flux concept weighted by defense capacity should be tested. Modeling of ozone effects on plants should include a measure for the plant defense capacity.

Agriculture is a source for three primary greenhouse gases (GHGs): CO2, CH4, and N2O. It can also be a sink for CO2 through C sequestration into biomass products and soil organic matter. We summarized the literature on GHG emissions and C sequestration, providing a perspective on how agriculture can reduce its GHG burden and how it can help to mitigate GHG emissions through conservation measures. Impacts of agricultural practices and systems on GHG emission are reviewed and potential trade-offs among potential mitigation options are discussed. Conservation practices that help prevent soil erosion, may also sequester soil C and enhance CH4 consumption. Managing N to match crop needs can reduce N2O emission and avoid adverse impacts on water quality. Manipulating animal diet and manure management can reduce CH4 and N2O emission from animal agriculture. All segments of agriculture have management options that can reduce agriculture's environmental footprint. Management options can be used to reduce agriculture's environmental impacts.

The experiment was carried out on a short rotation coppice culture of poplars (POP-EUROFACE, Central Italy), growing in a free air carbon dioxide enriched atmosphere (FACE). The specific objective of this work was to study whether elevated CO2 and fertilization (two CO2 treatments, elevated CO2 and control, two N fertilization treatments, fertilized and unfertilized), as well as the interaction between treatments caused an unbalanced nutritional status of leaves in three poplar species (P. x euramericana, P. nigra and P. alba). Finally, we discuss the ecological implications of a possible change in foliar nutrients concentration. CO2 enrichment reduced foliar nitrogen and increased the concentration of magnesium; whereas nitrogen fertilization had opposite effects on leaf nitrogen and magnesium concentrations. Moreover, the interaction between elevated CO2 and N fertilization amplified some element unbalances such as the K/N-ratio. CO2 enrichment reduced foliar nitrogen and increased the magnesium concentration in poplar.

Buffer capacity analysis of open atmospheric gas-liquid systems containing main acidic and basic atmospheric pollutants was carried out. Usually the buffer capacity is considered as a function of pH as an independent variable. In this work the buffer capacity is analysed including the dependence of pH on the composition of a system. Such an approach allows finding an important, from the viewpoint of atmospheric water acidification, relationship between the gas phase composition and the buffer capacity. It was found that buffer capacity of the open gas-liquid systems may be very high and it may cause the liquid phase pH to remain at low levels. The buffer capacity of the analysed systems is most strongly affected by the simultaneous presence of ammonia and strong acids in the gas phase. The higher concentrations of strong acid gases the lower NH₃ concentration is sufficient to achieve high buffer capacity. In the presence of strong acid gases, calcium ions affect both the buffer capacity and the liquid phase pH only at low NH₃ concentrations. High buffer capacity of open gas-liquid systems may be one of the reasons why the reduction in emissions of acidic gas pollutants has little effect on decrease in atmospheric water acidity.

The effects of ozone in four maple species, Acer campestre, A. opalus subsp. granatense, A. monspessulanum and A. pseudoplatanus were studied in OTC under two different experimental conditions: in charcoal filtered air (CF), and in non filtered air plus 30 ppb ozone (NF+30). The four species of maple showed contrasting sensitivity to ozone as demonstrated by visible injury development, gas exchange and chlorophyll a fluorescence, and growth measurements. Plant injury index (i.e. a combination of percentage of injured leaves and leaf surface affected) was more consistently related with physiological measurements than the onset of first symptom of visible injury. Differences in ozone sensitivity among species may be partly related to higher stomatal conductances in A. opalus and A. pseudoplatanus. In these two species, ozone produced significant reductions in CO₂ assimilation under saturating light conditions (A sat), stomatal conductance (g s), transpiration rate (T r) and Water Use Efficiency (WUE) (the latter also significantly declined in A. campestre) towards the end of summer, while intercellular CO₂ concentrations (C i) increased significantly. In asymptomatic leaves of A. opalus, neither stomatal limitation nor photoinhibitory damage (F v/F m) could explain the observed decline of A sat, and photosynthesis was down regulated by reducing the proportion of absorbed energy used in photochemistry (Φ PSII) at expenses of the energy dispersed non-photochemically (NPQ). Leaf N content also declined significantly in A. pseudoplatanus. Plants exposed to ozone showed a tendency to decrease growth, but it was not significant within the exposure period for any of the four species. The most sensitive species were A. opalus and A. pseudoplatanus, while the species with the smallest and more coriaceous leaves, A. monspessulanum, was the most resistant.