The effect of air pollutants on physiological processes in plants

Abstract. Important physiological processes, photosynthesis, respiration, carbon allocation and stomatal function are known to be affected by air pollutants. A wide range in sensitivity of photosynthesis both within and between species is evident from the literature for the pollutants sulphur dioxide, ozone, nitrogen oxide and hydrogen fluoride. Some of this variation is clearly due to genetic factors, but much is in response to differences in environmental conditions both prior to and during fumigation. Exposure of plants to mixtures of pollutants generally reduced the threshold at which effects were first detected and increased the level of inhibitory responses. In the majority of studies on stomatal responses to air pollutants, opening occurs at low concentrations, below the threshold for effects on photosynthesis, and closure occurs at injurious concentrations; this latter response often following the inhibition of photosynthesis. Effects on carbon allocation have been reported in response to air pollutants. Changes usually favour leaf development over root growth, which can compensate for a decline in net assimilation rate up to a certain point but may limit water uptake from soils with low moisture content. Future research into physiological effects of air pollutants should incorporate an integrated approach in which both key physiological parameters and growth parameters are measured together with estimates of the effective dose of pollutant. In this way, the underlying mechanisms to changes in growth and development will be more fully understood.     

Effects of air pollutants on proton and sucrose transport at the plasma membrane of Ricinus communis

The effects of the air pollutants O₃, SO₂ and NO₂ on aspects of sucrose/proton cotransport across the plasma membrane of Ricinus communis plants have been investigated. The H⁺-ATPase hydrolytic activity in cotyledon plasma membrane vesicles purified by phase partitioning showed small stimulations by Na₂SO₃ or NaNO₃ added separately or together to the assay medium. ATPase activity from plants pretreated by fumigation with SO₂ or O₃ also showed an increase, the effect of O₃ being quite marked. Plasma membrane H⁺-pumping in KI-treated microsomal fractions and medium acidification by intact cotyledons both showed small decreases in the presence of Na₂SO₃ or NaNO₂. Both Na₂SO₃ and NaNO₂ at high concentrations (2 mol m^–3) had significant effects on sucrose uptake by intact cotyledons, although sucrose efflux was unaffected. No significant effects on sucrose uptake or efflux by intact cotyledons were observed in plants pretreated by fumigation with SO₂ or O₃. Proton-coupled sucrose transport in isolated plasma membrane vesicles was inhibited in the presence of Na₂SO₃ or NaNO₂. However, both pollutants also significantly inhibited the uptake of acetate by the vesicles, indicating a dissipation of the pH gradient across the membrane. It was concluded that no specific aspect of the sucrose/proton cotransport mechanism was damaged by these air pollutants, and that the effects of these pollutants on carbohydrate partitioning are more likely to be due to general effects on membrane integrity or on other aspects such as leaf carbohydrate metabolism.     

The Effect of Nitrogen Nutrition on Cytokinin Activity and Free Amino Acids inBetula pendulaRoth, andAcer pseudoplatanusL.

A comparison was made of the levels of extractable cytokinin-likecompounds and free nitrate in the tissues of Betula pendulaand Acer pseudoplatanus at two levels of nitrogen nutrition.In further studies comparisons were made of the levels of cytokinin-likecompounds and free amino acids extracted from the tissues ofB. pendula supplied with nitrogen as ammonium sulphate, ammoniumnitrate, or calcium nitrate. These results were then relatedto growth differences between the treatments. B. pendula supplied with a low level of nitrogen as ammoniumnitrate continued to make slow growth whereas A. pseudoplatanusformed terminal resting buds after 2–3 weeks, furthergrowth being arrested. The low levels of extractable cytokinin-likecompounds found in the leaves of B. pendula receiving a lownitrogen supply were in contrast to the results from A. pseudoplatanus,where only a small reduction was found in response to low nitrogensupply. Analysis of the plant tissue showed that free nitrateand amino acids were depleted to a greater extent from B. pendulathan from A. pseudoplatanus under conditions of low nitrogensupply. It is suggested that the ability of B. pendula to continueactive growth with low nitrogen supply may be related to thereadiness with which nitrogen can be mobilized and re-circulatedin the plant, a process including sequential leaf senescence. Contrasting growth habits were seen in B. pendula in ammoniumnitrate- and ammonium sulphate-fed plants. Lateral shoot growthin ammonium sulphate-fed plants was completely inhibited andno detectable cytokinin activity was found in tissue extracts,whereas ammonium nitrate-fed plants grew rapidly, and showedconsiderable development of laterals. Changes in the levelsof individual amino acids show that the form in which nitrogenis taken up by plants affects the subsequent pathways of metabolism.     

The Sensitivity of Net Photosynthesis in Several Plant Species to Short-term Fumigation with Sulphur Dioxide

The effects of exposure of up to 2 h with sulphur dioxide ona range of plant species was observed by measuring changes inthe rate of net photosynthesis under closely controlled environmentalconditions. Ryegrass, Lolium perenne ‘S23’ was thespecies most sensitive to SO₂; significant inhibition was detectedat 200 nl l^–1. Fumigations at 300 nl l^–1 also inhibitedphotosynthesis in field bean (Vicia faba cv. ‘Three FoldWhite’ and ‘Blaze’) and in barley (Hordeumvulgare cv. ‘Sonja’). No effect was detected inwheat (Triticum aestivum cv. ‘Virtue’) at concentrationsup to 600 nl l^–1 SO₂, or in oil-seed rape (Brassica napuscv. ‘Rafal’) except at 800 nl l^–1 SO₂). Recoverycommenced immediately after the fumigation was terminated andwas complete within 2 h when inhibition had not exceeded 20%during the SO₂ treatment. Key words: Sulphur dioxide, short-term fumigation, photosynthesis     

The effect of open-air fumigation with SO2 and O3 on carbohydrate metabolism in Scots pine (Pinus sylvestris) and Norway spruce (Picea abies)

The carbohydrate metabolism of the needles of Scots pine (Pinus sylvestris) and Norway spruce (Picea abies) has been examined in trees that were exposed to SO₂, and O₃, in an open-air fumigation experiment located in the Liphook forest in southern England. Two-year-old seedlings were planted in 1985 in seven experimental plots. Five plots received fumigation treatments of SO₂, O₃ or a combination of these gases to give a 2 × 3 factorial design with one additional ambient plot Fumigation with SO₂, occurred from May 1987 to December 1990 and O₃, fumigation occurred from March to December 1988, May to December 1989 and February to December 1990. Five samples of needles for investigation of carbohydrate metabolism were taken between February and July 1989. The concentrations of soluble carbohydrates (including sucrose and hexoses) were greatly reduced in the needles taken from Scots pine growing in the treated plots, and were also reduced, but to a lesser extent, in the needles taken from Norway spruce. Little variation in the concentration of starch in the needles of either species was detected. The activities of the two final enzymes of sucrose synthesis, sucrose phosphate synthase and sucrose 6-phos-phate phosphatase, were greatly reduced in the needles of Scots pine and were also reduced, but to a lesser extent, in the needles of Norway spruce in the fumigated plots. These reductions could be correlated with decreases in rates of photosynthetic CO₂ assimilation determined by independent groups of researchers working on the Liphook site.