An inexpensive system for exposing plants in the field to elevated concentrations of CO2

An inexpensive, potentially mobile field exposure system is described which may be easily constructed by a small workshop. It may be operated as an open-top with a frustrum or covered with a polycarbonate ‘lid’. The system is cost-effective for CO₂ exposure work because the small size allows provision of CO₂-enriched atmospheres over prolonged periods at relatively low cost. A preliminary assessment of the chambers has been made and concentrations can be maintained at ±6% for a target atmosphere of 680 cm³ m^?3 CO₂ under normal operating conditions. Other chamber environmental conditions are reported.     

Physiological effects of long term exposure to low concentrations of SO2 and NH3 on poplar leaves

Shoots of poplar (Populus euramericana L. cv. Flevo) were exposed to filtered air, SO₂, NH₃ or a mixture of SO₂ and NH₃ for 7 weeks in fumigation chambers. After this exposure gas exchange measurements were carried out using a leaf chamber. As compared to leaves exposed to filtered air, leaves pretreated with 112 μg m^?3 SO₂ showed a small reduction in maximum CO₂ assimilation rate (P_max) and stomatal conductance (g_s). They also showed a slightly higher quantum yield and dark respiration. In addition, the fluorescence measurements indicated that the Calvin cycle of the leaves pretreated with 112 μg m^?3 SO₂ was more rapidly activated after transition from dark to light. An exposure to 64 μg m^?3 NH₃ had a positive effect on P_max, stomatal conductance and NH₃ uptake of the leaves. This positive effect was counteracted by an SO₂ concentration of 45 μg m^?3. The exposure treatments appeared to have no effect on the relationship between net CO₂-assimilation and g_s. Also, no injury of the leaf cuticle or of epidermal cells was observed. Resistance analysis showed that NH₃ transfer into the leaf can be estimated from data on the boundary layer and stomatal resistance for H₂O transfer and NH₃ concentration at the leaf surface, irrespective of whether the leaves are exposed for a short or long time to NH₃ or to a mixture of NH₃ and SO₂. In contrast SO₂ uptake into the leaves was only partly correlated to the stomatal resistance. The results suggest a large additional uptake of this gas by the leaves. The possibility of a difference in path length between SO₂ and H₂O molecules is proposed.     

Effect of nitrogen and phosphorus availability on the growth response of Eucalyptus grandis to high CO2

The response of Eucalyptus grandis seedlings to elevated atmospheric CO₂ concentrations was examined by growing seedlings at either 340 or 660 n mol CO₂ mol^-1 for 6 weeks. Graded increments of phosphorus and nitrogen fertilizers were added to a soil deficient in these nutrients to establish if the growth response to increasing nutrient availability was affected by CO₂ concentration. At 660 μmol CO₂ mol^-1, seedling dry weight was up to five times greater than at 340 μmol CO₂ mol^-1. The absolute response was largest when both nitrogen and phosphorus availability was high but the relative increase in dry weight was greatest at low phosphorus availability. At 340 μmol CO₂ mol^-1 and high nitrogen availability, growth was stimulated by addition of phosphorus up to 76 mg kg 1 soil. Further additions of phosphorus had little effect. However, at 660 μmol CO₂ mol^-1, growth only began to plateau at a phosphorus addition rate of 920mg kg^-1 soil. At 340 μmol CO₂ mol^-1 and high phosphorus availability, increasing nitrogen from 40 to 160mg kg^-1 soil had little effect on plant growth. At high CO₂, growth reached a maximum at between 80 and 160mg nitrogen kg^-1 soil. Total uptake of phosphorus was greater at high CO₂ concentration at all fertilizer addition rates, but nitrogen uptake was either lower or unchanged at high CO₂ concentration except at the highest nitrogen fertilizer rate. The shoot to root ratio was increased by CO₂ enrichment, primarily because the specific leaf weight was greater. The nitrogen and phosphorus concentration in the foliage was lower at elevated CO₂ concentration partly because of the higher specific leaf weight. These results indicate that critical foliar concentrations currently used to define nutritional status and fertilizer management may need to be reassessed as the atmospheric CO₂ concentration rises.     

Exposure to preindustrial, current and future atmospheric CO2 and temperature differentially affects growth and photosynthesis in Eucalyptus

To investigate if Eucalyptus species have responded to industrial-age climate change, and how they may respond to a future climate, we measured growth and physiology of fast- ( E. saligna ) and slow-growing ( E. sideroxylon ) seedlings exposed to preindustrial (290), current (400) or projected (650 μL L⁻¹) CO₂ concentration ([CO₂]) and to current or projected (current +4 °C) temperature. To evaluate maximum potential treatment responses, plants were grown with nonlimiting soil moisture. We found that: (1) E. sideroxylon responded more strongly to elevated [CO₂] than to elevated temperature, while E. saligna responded similarly to elevated [CO₂] and elevated temperature; (2) the transition from preindustrial to current [CO₂] did not enhance eucalypt plant growth under ambient temperature, despite enhancing photosynthesis; (3) the transition from current to future [CO₂] stimulated both photosynthesis and growth of eucalypts, independent of temperature; and (4) warming enhanced eucalypt growth, independent of future [CO₂], despite not affecting photosynthesis. These results suggest large potential carbon sequestration by eucalypts in a future world, and highlight the need to evaluate how future water availability may affect such responses.     

Effects of elevated CO2 on the foraging behavior of cotton bollworm, Helicoverpa armigera

Effects of elevated CO2 on the foraging behavior of cotton bollworm Helicoverpa arrnigera Hübner reared on milky grains of spring wheat grown in ambient, 550μL/L and 750μL/L CO2 concentration atmospheres in open-top chambers （OTC） were studied. The results indicated that： （i） elevated CO2 significantly affected both the type and amount of food eaten by H.arrnigera reared on milky grains of ambient CO2-grown wheat were significant higher than those for bollworm larvae reared on wheat grains grown in 550 and 750μL/L CO2 atmospheres; （ii） when bollworm larvae were reared on mixed milky grains from different CO2-grown wheat （food-choice condition）, larval duration increased significantly-pupal weight, adult longevity, and fecundity decreased significantly, comparing with those reared on milky grains of ambient CO2-grown wheat, 550μL/L CO2-grown wheat and 750μL/L CO2-grown wheat respectively; （iii） significant decreases in the contents of fructose and gross protein （GP） and significant increases in the contents of glucose, amylose, total saccharides （TSC）, TSC： GP ratio, free amino acids and soluble protein in the wheat grains with CO2 rising; （iv） and selected-foraging amount/food-choice index of cotton bollworm H.armigera were significantly positive correlated with the contents of fructose and GP of wheat grains, but they had significantly negative relationships with the contents of glucose, amylose, TSC and TSC： GP ratio of wheat grains.     

Growth of coniferous trees exposed to SO2 and O3 using an open-air fumigation system

Scots pine (Pinus sylvestris L.), Norway spruce (Picea abies (L.) Karst.) and Sitka spruce (Picea sitchensis Bong. Carr.) were planted as 2-year-old seedlings in an open-air fumigation facility at Liphook in southern England in March 1985. The soil was a humoferric podzol of pH 4. SO₂ fumigation began in May 1987 and continued until December 1990. Long-term mean SO₂ concentrations were 4,13 and 22 nmol mo^?1. Three plots, one at each SO₂ level, were also exposed to O₃ at an average of 1–3.times the ambient level. O₃ fumigation ran from March to December 1988, May to December 1989 and February to December 1990. Each species reacted differently to treatment. Scots pine showed no growth response to either pollutant, although other work on the site demonstrated a number of deleterious effects of SO₂ on this species, including increased leaf loss and foliar injury. Stem basal diameter growth of Norway spruce was depressed in SO₂-treated plots. In contrast, extension growth of shoots of Sitka spruce increased in SO₂-treated plots, in apparent response to codeposition of NH₃-N. However, diameter growth of Sitka spruce main stems did not increase. No effects of O₃ on growth were recorded for any species.     

Effects of SO2 on photosynthesis and ribulose bisphosphate carboxylase in pine tree seedlings

Fumigations of 4–7 week old seelings of Pinus silvestris , with ca 400 μg SO₂ m^-3 for 4–5 days resulted in a decrease both in net photosynthetic rate and in the levels of ribulose bisphosphate carboxylase activity of the primary needles. The effect on net photosynthesis was reversible. No visible damages were observed on the needles. Lower concentrations, ca 200 μg SO₂ m^-3, for ca 6 days inhibited net photosynthesis reversibly. The effect on net photosynthesis was not the result of stomata closure or of increased respiration. A dose-response relation for the inhibition of net photosynthesis and ribulose bisphosphate carboxylase is suggested. A similar relation was observed for the chlorophyll content of the needles. The reversible inhibition of photosynthesis was evident only at high quantum flux density, and the quantum yield of photosynthesis at rate limiting quantum flux was not affected. This was also suggested from an experiment with Scots pine in the field.     

THE COMBINED EFFECTS OF LOW TEMPERATURE AND SO2+NO2 POLLUTION ON THE NEW SEASON'S GROWTH AND WATER RELATIONS OF PICEA SITCHENSIS

Picea sitchensis (Bong.) Carr. seedlings were exposed to SO₂, NO₂ and SO₂+ NO₂ during dormancy in controlled environments, and were taken to night temperatures of 4, 0, −5, −10 and −15 °C in a freezer. Conditions in the freezer were carefully monitored during the low–temperature treatments. In two experiments, different photoenvironments and temperature regimes were imposed prior to the cold treatments, and different effects were observed. In the first, only limited frost hardiness was achieved and night temperatures of −15 °C were lethal. Temperatures of −5 and − 10 °C led to poor survival of lateral buds, particularly in plants exposed to 45 ppb SO₂. The poor bud break in plants exposed to SO₂ and to − 5 °C resulted in a loss of the effectiveness of this temperature as a chill requirement. Pressure-volume analysis showed that the shoots of plants exposed to NO₂ had greater elasticity (lower elastic moduli, e), so that loss of turgor occurred at lower relative water contents. In contrast, a hardening period (2 weeks in night/day temperatures of 3/10 °C and 8 h days at 50 μmol m⁻² s⁻¹ PAR) gave decreased elasticity and lower solute potentials of spruce shoots. In the second experiment, exposure to 30 ppb SO₂ and SO₂+ NO₂ led to slight, but consistent, increases in frost injury to the needles of plants frozen to − 5 and − 10 °C. The results suggest that the main interaction of low temperatures and winter pollutants may be on bud survival rather than on needle damage, but that effects are subtle, only occurring with certain combinations of pollutant dose and cold treatment.     

An in vivo analysis of the effect of SO2 fumigation on photosynthesis in Zea mays.

Fumigation of leaves with SO₂ can reduce the capacity for photosynthetic CO₂ uptake even in the absence of visible symptoms of damage. In vitro studies suggest that this invisible injury to intact leaves could be affected by damage to each of the main stages in the photosynthetic process. Reduced stomatal apertures may also reduce photosynthesis following SO₂ fumigation. The responses of CO₂ uptake by leaves to intercellular CO₂ concentration and to absorbed light provide information for quantitative separation of the in vivo contribution of the different stages of photosynthesis to reduction in overall rate. This study uses these techniques to examine the basis of reduction in CO₂ uptake in Zea mays cv. LG11 leaves following short-term fumigation with SO₂. Fumigation with 33 μmol m^–3 SO₂ for 30 min reduced light saturated CO₂ uptake by about one-third. An even greater reduction in light limited CO₂ uptake was observed and with no significant change in light absorptance this was attributed to a reduced quantum yield of photosynthesis. The light saturated CO₂ uptake rate and the stomatal conductance decreased in parallel. However, the relationship of CO₂ uptake to the intercellular CO₂ concentration suggested that the reduced stomatal conductance did not account for the reduced rate of CO₂ uptake following fumigation. Both the initial slope and plateau of this relationship were significantly reduced, suggesting that both carboxylation efficiency and capacity for regeneration of CO₂ acceptor were diminished by SO₂ fumigation. The operating intercellular CO₂ concentration indicated that both processes were co-limiting, before and after fumigation. The time required for induction of photosynthetic CO₂ uptake on illumination was approximately doubled following SO₂ fumigation, showing that fumigation impairs the ability of the photosynthetic apparatus to adapt to fluctuations in light level.