Effects of long-term atmospheric CO2 enrichment on the growth and fruit production of sour orange trees

In July of 1987, we planted eight 30-cm-tall sour orange tree seedlings in a field of Avondale loam at Phoenix, Arizona and enclosed them in pairs in clear-plastic-wall open-top chambers. Since 18 November of that year, we have continuously pumped ambient air of ≈400 ppmv [CO₂] through two of these enclosures, while through the other two we have continuously pumped air of ≈700 ppmv [CO₂]. By the end of the second year of the study, the trunk plus branch volume of the [CO₂]-enriched trees was ≈2.75 times greater than that of the ambient-treatment trees. Three years later, this factor had dropped to ≈2.0; but the decline in the [CO₂]-enriched/ambient-treatment ratio of trunk plus branch volume was nearly perfectly offset by the relative fruit production advantage enjoyed by the [CO₂]-enriched trees over that period. In Years 6, 7 and 8, however, there was a moderate drop in total productivity enhancement. This decline may be a delayed acclimation response, or it could be due to enhanced self-shading in the [CO₂]-enriched trees or to the fact that, starting early in Year 6, many branches of the [CO₂]-enriched trees grew all the way to the walls of their enclosures, so that many blossoms and young fruit were destroyed by intermittent physical trauma produced by the action of wind against the taut plastic in that year and in all succeeding years. Hence, we will have to maintain our experiment for several more years for this lateral growth obstruction to occur to the same degree in the ambient-air chambers as it has in the [CO₂]-enriched chambers, in order to determine the long-term equilibrium effects of atmospheric [CO₂] enrichment in a spatially confined environment.     

Seventeen years of carbon dioxide enrichment of sour orange trees: final results

The long-term responses of trees to elevated CO₂ are especially crucial (1) to mitigating the rate of atmospheric CO₂ increase, (2) to determining the character of future forested natural ecosystems and their spread across the landscape, and (3) to determining the productivity of future agricultural tree crops. Therefore, a long-term CO₂-enrichment experiment on sour orange trees was started in 1987, and the final results after 17 years are reported herein. Four sour orange trees ( Citrus aurantium L.) were grown from seedling stage at 300 μmol mol⁻¹ CO₂ above ambient in open-top, clear-plastic-wall chambers at Phoenix, AZ. Four control trees were similarly grown at ambient CO₂. All trees were supplied ample water and nutrients comparable with a commercial orchard. After a peak 2–4 years into the experiment, there was a productivity plateau at about a 70% enhancement of annual fruit and incremental wood production over the last several years of the experiment. When summed over the duration of the experiment, there was an overall enhancement of 70% of total biomass production. Much of the enhancement came from greater numbers of fruits produced, with no change in fruit size. Thicker trunks and branches and more branches and roots were produced, but the root/shoot ratio was unaffected. Also, there was almost no change in the elemental composition of the biomass produced, perhaps in part due to the minimal responsiveness of root-symbiotic arbuscular mycorrhizal fungi to the treatment.     

Elevated atmospheric CO2 alters wood production, wood quality and wood strength of Scots pine (Pinus sylvestris L) after three years of enrichment

Scots pine ( Pinus sylvestris L.) trees were grown in open top chambers for three years under ambient and elevated CO₂ concentrations. The trees were aged 3 y at the beginning of the CO₂ exposure, and the effects of the treatment on total stem volume, stem wood biomass, wood quality and wood anatomy were examined at the end of the exposure. The elevated CO₂ treatment lead to a 49% and 38% increase in stem biomass and stem wood volume, respectively. However, no significant effects of the elevated CO₂ treatment on wood density were observed, neither when green wood density was estimated from stem biomass and stem volume, nor when oven-dry wood density was measured on small wood samples. Under elevated CO₂ significantly wider growth rings were observed. The effect of elevated CO₂ on growth ring width was primarily the result of an increase in earlywood width. Wood compression strength decreased under elevated CO₂ conditions, which could be explained by significantly larger tracheids and the increased earlywood band, that has thinner walls and larger cavities. A significant decrease of the number of resin canals in the third growth ring was observed under the elevated treatment; this might indicate that trees produced and contained less resin, which has implications for disease and pest resistance. So, although wood volume yield in Scots pine increased significantly with elevated CO₂ after three years of treatment, wood density remained unchanged, while wood strength decreased. Whilst wood volume and stem biomass production may increase in this major boreal forest tree species, wood quality and resin production might decrease under future elevated CO₂ conditions.     

Stem wood properties of mature Norway spruce after 3 years of continuous exposure to elevated [CO2] and temperature

The objective of the study was to investigate the interactive effects of elevated atmospheric carbon dioxide concentration, [CO₂], and temperature on the wood properties of mature field-grown Norway spruce ( Picea abies (L.) Karst.) trees. Material for the study was obtained from an experiment in Flakaliden, northern Sweden, where trees were grown for 3 years in whole-tree chambers at ambient (365 μmol mol⁻¹) or elevated [CO₂] (700 μmol mol⁻¹) and ambient or elevated air temperature (ambient +5.6 °C in winter and ambient +2.8 °C in summer). Elevated temperature affected both wood chemical composition and structure, but had no effect on stem radial growth. Elevated temperature decreased the concentrations of acetone-soluble extractives and soluble sugars, while mean and earlywood (EW) cell wall thickness and wood density were increased. Elevated [CO₂] had no effect on stem wood chemistry or radial growth. In wood structure, elevated [CO₂] decreased EW cell wall thickness and increased tracheid radial diameter in latewood (LW). Some significant interactions between elevated [CO₂] and temperature were found in the anatomical and physical properties of stem wood (e.g. microfibril angle, and LW cell wall thickness and density). Our results show that the wood material properties of mature Norway spruce were altered under exposure to elevated [CO₂] and temperature, although stem radial growth was not affected by the treatments.     

Nodulation and nitrogenase activity in nitrogen-fixing woody plants stimulated by CO2 enrichment of the atmosphere

The responses of three species of nitrogen-fixing trees to CO₂ enrichment of the atmosphere were investigated under nutrient-poor conditions. Seedlings of the legume, Robinia pseudoacacia L. and the actinorhizal species, Alnus glutinosa (L.) Gaertn. and Elaeagnus angustifolia L. were grown in an infertile forest soil in controlled-environment chambers with atmospheric CO₂ concentrations of 350 μl ⁻¹ (ambient) or 700 μl ⁻¹. In R. pseudoacacia and A. glutinosa , total nitrogenase (N₂ reduction) activity per plant, assayed by the acetylene reduction method, was significantly higher in elevated CO₂, because the plants were larger and had more nodule mass than did plants in ambient CO₂. The specific nitrogenase activity of the nodules, however, was not consistently or significantly affected by CO₂ enrichment. Substantial increases in plant growth occurred with CO₂ enrichment despite probable nitrogen and phosphorus deficiencies. These results support the premises that nutrient limitations will not preclude growth responses of woody plants to elevated CO₂ and that stimulation of symbiotic activity by CO₂ enrichment of the atmosphere could increase nutrient availability in infertile habitats.     

Effects of elevated CO2-grown loblolly pine needles on the growth, consumption, development, and pupal weight of red-headed pine sawfly larvae reared within open-topped chambers

Seedlings of loblolly pine, Pinus taeda , were grown in open-topped chambers under four levels of CO₂: two ambient and two elevated. Larvae of the red-headed pine sawfly, Neodiprion lecontei , were reared from early instar to pupation, primarily on branches within chambers. Larval growth and mortality were assessed and leaf phytochemistry samples of immature and mature leaves collected weekly. Mature leaves grown under elevated CO₂ had significant reductions in leaf nitrogen and increases in non-structural carbohydrate contents, resulting in foliage being a poorer food source for larvae, i.e. higher carbohydrate:nitrogen ratio. Nutritional constituents of immature needles were unaffected by seedling CO₂ treatment. Volatile mono- and sesquiterpenes were unrelated to plant CO₂ treatments for either leaf age class. Larval consumption of immature needles significantly increased on seedlings grown under CO₂ enrichment, while mature needle consumption was not different between the treatments. The average weight gain per larva significantly declined in late instar larvae consuming elevated CO₂-grown needles. In spite of this reduced growth, neither the days to pupation nor pupal weights were different among the CO₂ treatments. This study suggests that enriched CO₂-induced alterations in pine needle phytochemistry can affect red-headed pine sawfly performance. However, compensatory measures by larvae, such as choosing to consume more nutritious immature needles, apparently helps offset enriched CO₂-induced reductions in the leaf quality of mature needles.     

Canopy photosynthesis of crops and native plant communities exposed to long-term elevated CO2

Abstract. There have been seven studies of canopy photosynthesis of plants grown in elevated atmospheric CO₂: three of seed crops, two of forage crops and two of native plant ecosystems. Growth in elevated CO₂ increased canopy photosynthesis in all cases. The relative effect of CO₂ was correlated with increasing temperature: the least stimulation occurred in tundra vegetation grown at an average temperature near 10°C and the greatest in rice grown at 43°C. In soybean, effects of CO₂ were greater during leaf expansion and pod fill than at other stages of crop maturation. In the longest running experiment with elevated CO₂ treatment to date, monospecific stands of a C₃ sedge, Scirpus olneyi (Grey), and a C₄ grass, Spartina patens (Ait.) Muhl., have been exposed to twice normal ambient CO₂ concentrations for four growing seasons, in open top chambers on a Chesapeake Bay salt marsh. Net ecosystem CO₂ exchange per unit green biomass (NCE_b) increased by an average of 48% throughout the growing season of 1988, the second year of treatment. Elevated CO₂ increased net ecosystem carbon assimilation by 88% in the Scirpus olneyi community and 40% in the Spartina patens community.     

Leaf isoprene emission rate as a function of atmospheric CO2 concentration

There is considerable interest in modeling isoprene emissions from terrestrial vegetation, because these emissions exert a principal control over the oxidative capacity of the troposphere. We used a unique field experiment that employs a continuous gradient in CO₂ concentration from 240 to 520 ppmv to demonstrate that isoprene emissions in Eucalyptus globulus were enhanced at the lowest CO₂ concentration, which was similar to the estimated CO₂ concentrations during the last Glacial Maximum, compared with 380 ppmv, the current CO₂ concentration. Leaves of Liquidambar styraciflua did not show an increase in isoprene emission at the lowest CO₂ concentration. However, isoprene emission rates from both species were lower for trees grown at 520 ppmv CO₂ compared with trees grown at 380 ppmv CO₂. When grown in environmentally controlled chambers, trees of Populus deltoides and Populus tremuloides exhibited a 30–40% reduction in isoprene emission rate when grown at 800 ppmv CO₂, compared with 400 ppmv CO₂. P. tremuloides exhibited a 33% reduction when grown at 1200 ppmv CO₂, compared with 600 ppmv CO₂. We used current models of leaf isoprene emission to demonstrate that significant errors occur if the CO₂ inhibition of isoprene is not taken into account. In order to alleviate these errors, we present a new model of isoprene emission that describes its response to changes in atmospheric CO₂ concentration. The model logic is based on assumed competition between cytosolic and chloroplastic processes for pyruvate, one of the principal substrates of isoprene biosynthesis.     

Elevated CO2 concentration, nitrogen use, and seed production in annual plants

Elevated atmospheric CO₂ concentration ([CO₂]) stimulates seed mass production in many species, but the extent of stimulation shows large variation among species. We examined (1) whether seed production is enhanced more in species with lower seed nitrogen concentrations, and (2) whether seed production is enhanced by elevated [CO₂] when the plant uses more N for seed production. We grew 11 annuals in open top chambers that have different [CO₂] conditions (ambient: 370 μmol mol⁻¹, elevated: 700 μmol mol⁻¹). Elevated [CO₂] significantly increased seed production in six out of 11 species with a large interspecific variation (0.84–2.12, elevated/ambient [CO₂]). Seed nitrogen concentration was not correlated with the enhancement of seed production by elevated [CO₂]. The enhancement of seed production was strongly correlated with the enhancement of seed nitrogen per plant caused by increased N acquisition during the reproductive period. In particular, legume species tended to acquire more N and produced more seeds at elevated [CO₂] than non-nitrogen fixing species. Elevated [CO₂] little affected seed [N] in all species. We conclude that seed production is limited primarily by nitrogen availability and will be enhanced by elevated [CO₂] only when the plant is able to increase nitrogen acquisition.     

Wood composition and energy content in a poplar short rotation plantation on fertilized agricultural land in a future CO2 atmosphere

To study the influence of elevated CO₂ and nitrogen (N) fertilization on wood properties and energy, Populus × euramericana trees were exposed to ambient CO₂ (about 370 μmol mol⁻¹ CO₂) or elevated CO₂ (about 550 μmol mol⁻¹ CO₂) using Free Air CO₂ Enrichment (FACE) technology in combination with two N levels. Elevated CO₂ was maintained for 5 years. After three growing seasons, the plantation was coppiced, one half of each experimental plot was fertilized and secondary sprouts were harvested after two growing seasons. Fourier transform infrared (FT-IR) spectra of wood revealed significant effects of both elevated CO₂ and N fertilization on wood chemistry, in particular, significant increases in lignin and decreases in N content. These results were corroborated by chemical analysis. Neither elevated CO₂ nor N fertilization affected the calorific value of wood, which was 19.3 MJ kg⁻¹. N fertilization enhanced the energy production per land area by 16–69% because of higher aboveground woody biomass production than on nonfertilized land. Estimates indicate that high yielding poplar short rotation cultivation may significantly contribute as an alternative feedstock for energy production.     

Does soil nitrogen influence growth,water transport and survival of snow gum (Eucalyptus pauciflora Sieber ex Sprengel.) under CO2 enrichment?

Eucalyptus pauciflora Sieber ex Sprengel. (snow gum) was grown under ambient (370  µ L L⁻¹) and elevated (700  µ L L⁻¹) atmospheric [CO₂] in open-top chambers (OTCs) in the field and temperature-controlled glasshouses. Nitrogen applications to the soil ranged from 0.1 to 2.75 g N per plant. Trees in the field at high N levels grew rapidly during summer, particularly in CO₂-enriched atmosphere, but suffered high mortality during summer heatwaves. Generally, wider and more numerous secondary xylem vessels at the root–shoot junction in CO₂-enriched trees conferred fourfold higher below-ground hydraulic conductance. Enhanced hydraulic capacity was typical of plants at elevated [CO₂] (in which root and shoot growth was accelerated), but did not result from high N supply. However, because high rates of N application consistently made trees prone to dehydration during heatwaves, glasshouse studies were required to identify the effect of N nutrition on root development and hydraulics. While the effects of elevated [CO₂] were again predominantly on hydraulic conductivity, N nutrition acted specifically by constraining deep root penetration into soil. Specifically, 15–40% shallower root systems supported marginally larger shoot canopies. Independent changes to hydraulics and root penetration have implications for survival of fertilized trees under elevated atmospheric [CO₂], particularly during water stress.     

The influence of elevated CO2 on species phenology, growth and reproduction in a Mediterranean old-field community

We studied the effects on the phenology, growth and reproduction of 19 Mediterranean species, of elevating the atmospheric CO₂ concentration ([CO₂]) to twice-ambient. Intact monoliths were taken from an old-field and put, during a six month growing season, into growth chambers in which external climatic conditions were mimicked and [CO₂] was regulated. Fruit set time was significantly changed in six species under elevated [CO₂] and leaf and branch senescence accelerated in most species. Grasses had fewer leaves and legumes were more branched at peak production under elevated [CO₂] than under ambient. Plant seed number was not significantly changed under elevated [CO₂], whereas the reproductive effort of grasses was significantly depressed. Reproductive and vegetative characteristics showed related responses to [CO₂], as species with enhanced biomass had a hastened fruit set time, a higher number of fruits per plant and a higher reproductive biomass under elevated [CO₂] than under ambient conditions, while species with depressed biomass had a delayed fruit set time, a lower number of fruits per plant and a lower reproductive biomass. Our results also show a high interspecific variability in [CO₂] response, but some trends emerged at the family level: the production of vegetative and reproductive modules were depressed in grasses and slightly stimulated in legumes.     

Growth response of branches of Picea sitchensis to four years exposure to elevated atmospheric carbon dioxide concentration

Branch bags were used to expose branches on mature Sitka spruce trees to either ambient [CO₂] (A) or elevated [CO₂] (E) for 4 yr. This paper reports the effects of this treatment on the growth, development and phenology of the branches, including shoot expansion, shoot numbers, needle dimensions, needle numbers and stomatal density. The effect of elevated [CO₂] on the relationship between leaf area and sapwood area was investigated. Exposure to elevated [CO₂] doubled photosynthetic rates in current-year shoots and, despite some down-regulation, 1-yr-old E shoots also had higher rates of photosynthesis than their A counterparts. Thus, the amount of assimilate fixed by E branches was substantially more than that fixed by A branches; however, this increase in the local production of assimilate did not lead to an increase in non-structural carbohydrate or stimulate growth or meristematic activity within the E branches. There was a very consistent relationship between leaf area and stem cross-sectional area that was not influenced by [CO₂]. However, unbagged branches had thicker stems than bagged branches, resulting in a slightly lower ratio of leaf area to cross-sectional area. The implications of the results for the modelling of growth and allocation and the potential utility of the branch bag technique are discussed.     

Stomata of trees growing in CO2-enriched air show reduced sensitivity to vapour pressure deficit and drought

Stomatal conductance ( g _s) and photosynthetic rate ( A ) were measured in young beech ( Fagus sylvatica ), chestnut ( Castanea sativa ) and oak ( Quercus robur ) growing in ambient or CO₂-enriched air. In oak, g _s was consistently reduced in elevated CO₂. However, in beech and chestnut, the stomata of trees growing in elevated CO₂ failed to close normally in response to increased leaf-to-air vapour pressure deficit (LAVPD). Consequently, while g _s was reduced in elevated CO₂ on days with low LAVPD, on warm sunny days (with correspondingly high LAVPD) g _s was unchanged or even slightly higher in elevated CO₂. Furthermore, during drought, g _s of beech and chestnut was unresponsive to [CO₂], over a wide range of ambient LAVPD, whereas in oak g _s was reduced by an average of 50% in elevated CO₂. Stimulation of A by elevated CO₂ in beech and chestnut was restricted to days with high irradiance, and was greatest in beech during drought. Hence, most of the additional carbon gain in elevated CO₂ was made at the expense of water economy, at precisely those times (drought, high evaporative demand) when water conservation was most important. Such effects could have serious consequences for drought tolerance, growth and, ultimately, survival as atmospheric [CO₂] increases.     

Shade‐tolerance as a predictor of responses to elevated CO2 in trees

Evidence from 10 studies comparing angiosperm trees and 5 studies comparing conifers of differing shade‐tolerance was analysed. The number of intraphyletic comparisons in which the more shade‐tolerant species showed the greater relative increase of biomass in elevated CO₂ was significantly higher than would be expected by chance alone. It is suggested that more shade‐tolerant species are inherently better disposed, in terms of plant architecture and partitioning of biomass and nitrogen, to utilise resources (light, water, nutrients) that are potentially limiting in elevated CO₂ and that these traits are responsible for the interaction between shade‐tolerance and CO₂ concentration. Compared with less shade‐tolerant angiosperm trees, more shade‐tolerant angiosperm species generally have a lower leaf area ratio in ambient CO₂ and show a smaller relative reduction in elevated CO₂. Furthermore, leaf nitrogen content is usually lower in more shade‐tolerant angiosperm species and tends to be more strongly reduced by elevated CO₂ in those species. Within angiosperm trees, more shade‐tolerant species showed a stronger stimulation of net leaf photosynthetic rate in most experiments, but this trend was not significant.     

Intraspecific variation in the response of rice (Oryza sativa) to increased CO2– photosynthetic, biomass and reproductive characteristics

Two rice ( Oryza sativa L.) cultivars of contrasting morphologies, IR-36 and Fujiyama-5, were exposed to ambient (360 μl l⁻¹) and ambient plus 300 μl l⁻¹ CO₂ from time of emergence until ca 50% grain fill at the Duke University Phytotron, Durham, North Carolina. Exposure to increased CO₂ resulted in about a 50% increase in the photosynthetic rate for both cultivars and photosynthetic enhancement was still evident after 3 months of exposure to a high CO₂ environment. The photosynthetic response at 5% CO₂ and the response of CO₂ assimilation (A) to internal CO₂ (C_i) suggest a reallocation of biochemical resources from RuBP carboxylation to RuBP regeneration. Increases in total plant biomass at elevated CO₂ were approximately the same in both cultivars, although differences in allocation patterns were noted in root/shoot ratio. Differences in reproductive characteristics were also observed between cultivars at an elevated CO₂ environment with a significant increase in harvest index for IR-36 but not for Fujiyama-5. Changes in carbon allocation in reproduction between these two cultivars suggest that lines of rice could be identified that would maximize reproductive output in a future high CO₂ environment.     

The cellular basis of guard cell sensing of rising CO2

Numerous studies conducted on both whole plants and isolated epidermes have documented stomatal sensitivity to CO₂. In general, CO₂ concentrations below ambient stimulate stomatal opening, or an inhibition of stomatal closure, while CO₂ concentrations above ambient have the opposite effect. The rise in atmospheric CO₂ concentrations which has occurred since the industrial revolution, and which is predicted to continue, will therefore alter rates of transpirational water loss and CO₂ uptake in terrestrial plants. An understanding of the cellular basis for guard cell CO₂ sensing could allow us to better predict, and perhaps ultimately to manipulate, such vegetation responses to climate change. However, the mechanisms by which guard cells sense and respond to the CO₂ signal remain unknown. It has been hypothesized that cytosolic pH and malate levels, cytosolic Ca²⁺ levels, chloroplastic zeaxanthin levels, or plasma-membrane anion channel regulation by apoplastic malate are involved in guard cell perception and response to CO₂. In this review, these hypotheses are discussed, and the evidence for guard cell acclimation to prevailing CO₂ concentrations is also considered.     

Gas exchange and carbon isotope composition of Ananas comosus in response to elevated CO2 and temperature

Ananas comosus L. (Merr.) (pineapple) was grown at three day/night temperatures and 350 (ambient) and 700 (elevated) μ mol mol^–1 CO₂ to examine the interactive effects of these factors on leaf gas exchange and stable carbon isotope discrimination ( Δ ,‰). All data were collected on the youngest mature leaf for 24 h every 6 weeks. CO₂ uptake (mmol m^–2 d^–1) at ambient and elevated CO₂, respectively, were 306 and 352 at 30/20 °C, 175 and 346 at 30/25 °C and 187 and 343 at 35/25 °C. CO₂ enrichment enhanced CO₂ uptake substantially in the day in all environments. Uptake at night at elevated CO₂, relative to that at ambient CO₂, was unchanged at 30/20 °C, but was 80% higher at 30/25 °C and 44% higher at 35/25 °C suggesting that phosphoenolpyruvate carboxylase was not CO₂-saturated at ambient CO₂ levels and a 25 °C night temperature. Photosynthetic water use efficiency (WUE) was higher at elevated than at ambient CO₂. Leaf Δ -values were higher at elevated than at ambient CO₂ due to relatively higher assimilation in the light. Leaf Δ was significantly and linearly related to the fraction of total CO₂ assimilated at night. The data suggest that a simultaneous increase in CO₂ level and temperature associated with global warming would enhance carbon assimilation, increase WUE, and reduce the temperature dependence of CO₂ uptake by A. comosus .     

Water vapour fluxes and their impact under elevated CO2 in a C4-tallgrass prairie

We measured leaf-level stomatal conductance, xylem pressure potential, and stomate number and size as well as whole plant sap flow and canopy-level water vapour fluxes in a C4-tallgrass prairie in Kansas exposed to ambient and elevated CO₂. Stomatal conductance was reduced by as much as 50% under elevated CO₂ compared to ambient. In addition, there was a reduction in stomate number of the C4 grass, Andropogon gerardii Vitman, and the C3 dicot herb, Salvia pitcheri Torr., under elevated CO₂ compared to ambient. The result was an improved water status for plants exposed to elevated CO₂ which was reflected by a less negative xylem pressure potential compared to plants exposed to ambient CO₂. Sap flow rates were 20 to 30% lower for plants exposed to elevated CO₂ than for those exposed to ambient CO₂. At the canopy level, evapotranspiration was reduced by 22% under elevated CO₂. The reduced water use by the plant canopy under elevated CO₂ extended the photosynthetically-active period when water became limiting in the ecosystem. The result was an increased above- and belowground biomass production in years when water stress was frequent.     

Effects of elevated CO2 concentration on photosynthesis, respiration and carbohydrate status of coppice Populus hybrids

To determine how increased atmospheric CO₂ will affect the physiology of coppiced plants, sprouts originating from two hybrid poplar clones ( Populus trichocarpa × P. deltoides - Beaupre and P. deltoides × P. nigra - Robusta) were grown in open-top chambers containing ambient or elevated (ambient + 360 μmol mol⁻¹) CO₂ concentration. The effects of elevated CO₂ concentration on leaf photosynthesis, stomatal conductance, dark respiration, carbohydrate concentration and nitrogen concentration were measured. Furthermore, dark respiration of leaves was partitioned into growth and maintenance components by regressing specific respiration rate vs specific growth rate. Sprouts of both clones exposed to CO₂ enrichment showed no indication of photosynthetic down-regulation. During reciprocal gas exchange measurements, CO₂ enrichment significantly increased photosynthesis of all sprouts by approximately 60% ( P < 0.01) on both an early and late season sampling date, decreased stomatal conductance of all sprouts by 10% ( P < 0.04) on the early sampling date and nonsignificantly decreased dark respiration by an average of 11%. Growth under elevated CO₂ had no consistent effect on foliar sugar concentration but significantly increased foliar starch by 80%. Respiration rate was highly correlated with both specific growth rate and percent nitrogen. Long-term CO₂ enrichment did not significantly affect the maintenance respiration coefficient or the growth respiration coefficient. Carbon dioxide enrichment affected the physiology of the sprouts the same way it affected these plants before they were coppiced.