In situ CO2 gas-exchange in fruits of a tropical tree,Durio zibethinus Murray

We examined the in situ CO₂ gas-exchange of fruits of a tropical tree, Durio zibethinus Murray, growing in an experimental field station of the Universiti Pertanian Malaysia. Day and night dark respiration rates were exponentially related to air temperature. The temperature dependent dark respiration rate showed a clockwise loop as time progressed from morning to night, and the rate was higher in the daytime than at night. The gross photosynthetic rate was estimated by summing the rates of daytime dark respiration and net photosynthesis. Photosynthetic CO₂ refixation, which is defined as the ratio of gross photosynthetic rate to dark respiration rate in the daytime, ranged between 15 and 45%. The photosynthetic CO₂ refixation increased rapidly as the temperature increased in the lower range of air temperature T _c (T _c <28.5 °C), while it decreased gradually as the temperature increased in the higher range (T _c 28.5 °C). Light dependence of photosynthetic CO₂ refixation was approximated by a hyperbolic formula, where light saturation was achieved at 100 mol m^–2 s^–1 and the asymptotic CO₂ refixation was determined to be 37.4%. The estimated gross photosynthesis and dark respiration per day were 1.15 and 4.90 g CO₂ fruit^–1, respectively. Thus the CO₂ refixation reduced the respiration loss per day by 23%. The effect of fruit size on night respiration rate satisfied a power function, where the exponent was larger than unity.     

Effects of long-term elevated atmospheric carbon dioxide onLolium perenne andTrifolium repens,using a simple photosynthesis model

Changes in gross canopy photosynthetic rate (PGc), produced by long-term exposure to an elevated atmospheric CO₂ level (626±50 µmol mol^-1), were modelled forLolium perenne L. cv. Vigor andTrifolium repens L. cv. Blanca, using a simple photosynthesis model, based on biochemical and physiological information (leaf gross CO₂ uptake in saturating light, P_max, and leaf quantum efficiency, ) and structural vegetation parameters (leaf area index, LAI, canopy extinction coefficient, k, leaf transmission, M). Correction of PGc for leaf respiration allowed comparison with previously measured canopy net CO₂ exchange rates, with the average divergence from model prediction amounting to about 6%. Sensitivity analysis showed that for a three-week old canopy, the PGc increase in high CO₂ could be attributed largely to changes in P_max and , while differences in canopy architecture were no longer important for the PGc-stimulation (which they were in the early growth stages). As a consequence of this increasing LAI with canopy age, the gain of daytime CO₂ uptake is progressively eroded by the increasing burden of canopy respiration in high-CO₂ grownLolium perenne. Modelling canopy photosynthesis in different regrowth stages after cutting (one week, two weeks,...), revealed that the difference in a 24-h CO₂ balance between the ambient and the high CO₂ treatment is reduced with regrowth time and completely disappears after 6 weeks.Abbreviations C350 ambient CO₂ treatment - C625 high CO₂ treatment - k canopy extinction coefficient - LAI leaf area index - LAI_max fitted LAI-maximum - M leaf transmission - NCER net CO₂ exchange rate - PGc gross canopy photosynthetic rate - Q photosynthetic photon flux density - Q₀ photosynthetic photon flux density at the top of the canopy - RDc canopy dark respiration rate - RDl leaf dark respiration rate - t regrowth time after cutting - T air temperature - leaf quantum efficiency - _LAI rate of initial LAI-increase with time     

Woody tissue maintenance respiration of four conifers in contrasting climates

We estimate maintenance respiration for boles of four temperate conifers (ponderosa pine, western hemlock, red pine, and slash pine) from CO₂ efflux measurements in autumn, when construction respiration is low or negligible. Maintenance respiration of stems was linearly related to sapwood volume for all species; at 10°C, respiration per unit sapwood volume ranged from 4.8 to 8.3 mol CO₂ m^–3 s^–1. For all sites combined, respiration increased exponentially with temperature (Q ₁₀ =1.7, r ²=0.78). We estimate that maintenance respiration of aboveground woody tissues of these conifers consumes 52–162 g C m^–2 y^–1, or 5–13% of net daytime carbon assimilation annually. The fraction of annual net daytime carbon fixation used for stem maintenance respiration increased linearly with the average annual temperature of the site.     

Effects of daytime carbon dioxide concentration on dark respiration in rice

Rising atmospheric carbon dioxide concentration ([CO₂]) has generated considerable interest in the response of agricultural crops to [CO₂]. The objectives of this study were to determine the effects of a wide range of daytime [CO₂] on dark respiration of rice (Oryza sativa L. cv. IR-30). Rice plants were grown season-long in naturally sunlit plant growth chambers in subambient (160 and 250), ambient (330), or super-ambient (500, 660 and 900 μmol CO₂ mol^?1 air) [CO₂] treatments. Canopy dark respiration, expressed on a ground area basis (R_d) increased with increasing [CO₂] treatment from 160 to 500 μmol mol^?1 treatments and was very similar among the superambient treatments. The trends in R_d over time and in response to increasing daytime [CO₂] treatment were associated with and similar to trends previously described for photosynthesis. Specific respiration rate (R_dw) decreased with time during the growing season and was higher in the subambient than the ambient and superambient [CO₂] treatments. This greater R_dw in the subambient [CO₂] treatments was attributed to a higher specific maintenance respiration rate and was associated with higher plant tissue nitrogen concentration.     

The contribution of crassulacean acid metabolism to the annual productivity of two aquatic vascular plants

Summary Net annual productivity and annual carbon budgets were determined for populations of Littorella uniflora var. americana and Isoetes macrospora in a mesotrophic and oligotrophic lake in northern Wisconsin, to assess the contribution of Crassulacean Acid Metabolism (CAM) to annual productivity of the species in their natural environment. Nocturnal carbon accumulation (CAM), daytime uptake of external CO₂ via the C₃ mechanism, and refixation of endogenously generated CO₂ from daytime respiration were the sources of carbon income. CAM activity as diurnal acid rhythms reached maxima of 89 to 182 eq·g^-1 leaf fresh weight for the various populations.Maximum rates of daytime ¹⁴C uptake ranged from 0.56 to 1.46 mg C·g^-1 leaf dry wt.·h^-1 for the study populations. Refixation of daytime respired CO₂ averaged 37% for the four populations. Carbon loss was due largely to dark respiration, during the day and night. Nocturnal carbon accumulation, daytime CO₂ uptake and 24-h dark respiration were of similar magnitude, indicating dark respiration was equivalent to 50% of gross photosynthesis.Net annual production was measured for each population by following leaf turnover. Turnover rates for the Littorella populations were 1.56 and 1.72·yr^-1, and for the Isoetes populations, 0.85 and 1.00·yr^-1. Measured net annual productivity and calculated net annual productivity (based on carbon exchange) agreed within an average of 12% for the four populations. While CAM activity was greater for the more productive population of each species, the results suggest that the contribution of CAM to annual productivity is greater for the less productive population of each species. CAM contributed 45 to 55% of the annual carbon gain for the study populations.     

Photosynthetic performance of vegetative and reproductive structures of green hellebore (<Emphasis Type="Italic">Helleborus viridis</Emphasis> L. agg.)

Photosynthetic irradiance response of vegetative and reproductive structures of the green-flowered deciduous perennial green hellebore was studied by the comparative use of chlorophyll (Chl) fluorescence techniques and gas exchange measurements. All the Chl-containing organs (leaves, sepals, stalks, and fruits) examined were photosynthetically active showing high intrinsic efficiencies of photosystem 2 (F_v/F_m: 0.75–0.79) after dark adaptation. Even in the smaller fertile and sterile parts of the flower (nectaries and anthers) a remarkable photosynthetic competence was detected. With increasing photon flux densities (PFD) electron transport rates, actual quantum yields, and photochemical quenching coefficients of the main photosynthetic organs decreased in the order: leaf>sepal>fruit>stalk. At moderate to high PFDs the sepals achieved maximum electron transport rates corresponding to about 80 % of concomitant mature leaves. In contrast, maximum net photosynthetic rate of the sepals [2.3 mol(CO₂) m^–2 s^–1] were less than one fourth of the leaves [10.6 mol(CO₂) m^–2 s^–1]. This difference is explained by a 70–80 % lower stomatal density of sepals in comparison to leaves. As the basal leaves emerge late during fruit development, the photosynthetically active sepals are a major source of assimilates, contributing more than 60 % of whole-plant CO₂ gain in early spring. The ripening dehiscent fruits are characterized by an effective internal re-fixation of the respirational carbon loss and thus additionally improve the overall carbon budget.     

Metabolism of <Superscript>14</Superscript>C-glycine as a substrate for photorespiration of the leaf at different developmental stages of ephemeroides

The metabolism of ¹⁴C-glycine (a substrate for photorespiration) was studied in the light and in darkness under natural CO₂ concentration (0.03%) in the leaves of ephemeroides Scilla sibirica Haw. and Ficaria verna Huds. at different developmental stages. Using one and the same sample, potential photosynthesis (at 1% CO₂), true photosynthesis (at 0.03% CO₂), and leaf respiratory capacity were measured by the radiometric and manometric methods, respectively. All measurements were performed at 15°C, an average temperature during ephemer growth. It was found that, in the white zone of the Scilla leaf, the rate of CO₂ evolution resulting from metabolization of exogenous ¹⁴C-glycine was similar in the light and in darkness. In the green zone of the Scilla leaf and in the green leaf of Ficaria, both ¹⁴C-glycine absorption and ¹⁴CO₂ evolution were lower in the light as compared with darkness, which is explained by CO₂ reassimilation. In all treatments of both plant species, a specific inhibitor of glycine decarboxylase complex (GDC), aminoacetonitrile (5 mM) suppressed CO₂ evolution by 20–40%. It was concluded that in ephemeroides mitochondrial GDC, responsible for CO₂ evolution in photorespiration, is formed at the earliest stage of leaf development. This indicates that photorespiration can occur simultaneously with the development of the leaf photosynthetic activity. On the basis of the assumption that carbon losses in the form of CO₂ evolved during photorespiration comprise 25% of true photosynthesis, it was calculated that, in ephemer leaves, the highest rates of photorespiration and photosynthesis were attained during flowering when the leaf area was the largest and the rate of dark respiration was reduced by 1.5–2.0 times. The highest rates of dark respiration were observed in the beginning of growth. In senescing leaves by the end of the plant vegetation, potential photosynthesis and true photosynthesis were reduced, whereas dark respiration remained essentially unchanged. It is concluded that the high rates of potential and true photosynthesis are characteristic of ephemeroides when they complete their short developmental program in early spring (at 15°C); theoretically, photorespiration also occurs at a high rate during this period, when this process provides for a defense against the threat of photoinhibition at low temperature and high insolation.     

Photosynthesis by inflated pods of a desert shrub,Isomeris arborea

Summary The photosynthetic capacity and carbon metabolism of the fruits of Isomeris arborea (Capparidaceae), an evergreen shrub endemic to the desert and coastal habitats of Southern California and Baja California, are described. The inflated structure of the pods of I. arborea provides a model system for experimental studies of fruit photosynthesis in native plants since the gas concentration of the internal space can be manipulated and monitored separately from the external pod environment. CO₂ released by seed respiration is partially contained in the inner gas space of the pods, resulting in an elevated CO₂ environment inside the fruit (500 to 4000 mol mol^–1 depending on the stage of fruit development). A portion of this CO₂ is assimilated by the inner layers of the pericarp, but a larger fraction leaks out. The photosynthetic layers of the pericarp use two different sources of CO₂: the exocarp fixes exogenous CO₂ while the endocarp fixes CO₂ released by seed respiration into the pod cavity. Even though the total weight of the fruit increases during development, the combined rates of fixation of externally and internally supplied CO₂ remained constant (10–11 mol CO₂ pod^–1 h^–1). After the pods attain maximum volume, the major change in gas exchange that takes place during fruit growth is a gradual increase in the amount of respiratory CO₂ released by the seeds. This shifts the CO₂ balance of the fruit from positive, in young fruits, to negative in mature fruits. Pericarp photosynthesis helped support not only the cost of fruit maintenance, but also the cost of fruit growth, particularly during the first stages of fruit development. During later fruiting stages insufficient carbon is fixed to fully supply either respiration or growth.     

Effect of fruiting on carbon budgets of apple tree canopies

Summary Carbon budgets were calculated from net photosynthesis and dark respiration measurements for canopies of field-grown, 3-year-old apple trees (Malus domestica Borkh.) with maximum leaf areas of 5.4 m² in a temperature-controlled Perspex tree chamber, measured in situ over 2 years (July 1988 to October 1990) by computerized infrared gas analysis using a dedicated interface and software. Net photosynthesis (Pn) and carbon assimilation per leaf area peaked at respectively 8.3 and 7.7 mol CO₂ m^–2 s^–1 in April. Net photosynthesis (Pn) and dark respiration (Rd) per tree peaked at 3.6 g CO₂ tree^–1 h^–1 (Pn) and 1.2 g CO₂ tree^–1 h^–1 (Rd), equivalent to 4.2 mol CO₂ (Pn) and 1.4 mol CO₂ (Rd) m^–2 s^–1 with maximum carbon gain per tree in August and maximum dark respiration per tree in October 1988 and 1989. In May 1990, a tree was deblossomed. Pn (per tree) of the fruiting apple tree canopy exceeded that of the non-fruiting tree by 2–2.5 fold from June to August 1990, attributed to reduced photorespiration (RI), and resulting in a 2-fold carbon gain of the fruiting over the non-fruiting tree. Dark respiration of the fruiting tree canopy progressively exceeded, with increasing sink strength of the fruit, by 51% (June–August), 1.4-fold (September) and 2-fold (October) that of the non-fruiting tree due to leaf (i. e. not fruit) respiration to provide energy (a) to produce and maintain the fruit on the tree and (b) thereafter to facilitate the later carbohydrate translocation into the woody perennial parts of the tree. The fruiting tree reached its optium carbon budget 2–4 weeks earlier (August) then the non-fruiting tree (September 1990). In the winter, the trunk respired 2–100 g CO₂ month^–1 tree^–1. These data represent the first long-term examination of the effect of fruiting without fruit removal which shows increased dark respiration and with the increase progressing as the fruit developed.     

Photosynthetic CO<Subscript>2</Subscript> uptake in seedlings of two tropical tree species exposed to oscillating elevated concentrations of CO<Subscript>2</Subscript>

Do short-term fluctuations in CO₂ concentrations at elevated CO₂ levels affect net CO₂ uptake rates of plants? When exposed to 600 μl CO₂ l^?1, net CO₂ uptake rates in shoots or leaves of seedlings of two tropical C₃ tree species, teak (Tectona grandis L. f.) and barrigon [Pseudobombax septenatum (Jacq.) Dug.], increased by 28 and 52% respectively. In the presence of oscillations with half-cycles of 20 s, amplitude of ca. 170 μl CO₂ l^?1 and mean of 600 μl CO₂ l^?1, the stimulation in net CO₂ uptake by the two species was reduced to 19 and 36%, respectively, i.e. the CO₂ stimulation in photosynthesis associated with a change in exposure from 370 to 600 μl CO₂ l^?1 was reduced by a third in both species. Similar reductions in CO₂-stimulated net CO₂ uptake were observed in T. grandis exposed to 40-s oscillations. Rates of CO₂ efflux in the dark by whole shoots of T. grandis decreased by 4.8% upon exposure of plants grown at 370 μl CO₂ l^?1 to 600 μl CO₂ l^?1. The potential implications of the observations on CO₂ oscillations and dark respiration are discussed in the context of free-air CO₂ enrichment (FACE) systems in which short-term fluctuations of CO₂ concentration are a common feature.     

Respiration of the growing shoots of Scots pine

The respiratory CO₂ exchange and the growth of the annual shoots were followed in Scots pine (Pinus sylvestris L.) trees growing under extreme continental forest-steppe conditions near the lake Baikal. The temperature coefficient of dark respiration (Q₁₀) in growing shoots dropped down from 3.2–4.0 (in the temperature range of 10–20°C) to 1.5–2.0 (in the temperature range of 20–30°C). The changes in averaged daily respiration rates correlated with the changes in shoot growth increments and temperature (with the multiple determination coefficient of 0.94). Growth respiration of the axial shoots during the phenophase reached 80% of the total respiration costs, with the coefficients of growth respiration and maintenance respiration 0.32 and 0.021. In young crown shoots, the average value of CO₂ evolution in the light combined for the whole observation period (years 1976–2004) was about 1 kg/dm², that is 9% of CO₂ evolution from the trunk surface.     

16O2/18O2 analysis of oxygen exchange in Dunaliella tertiolecta. Evidence for the inhibition of mitochondrial respiration in the light

A mass spectrometric ¹⁶O₂/¹⁸O₂-isotope technique was used to analyse the rates of gross O₂ evolution, net O₂ evolution and gross O₂ uptake in relation to photon fluence rate by Dunaliella tertiolecta adapted to 0.5, 1.0, 1.5, 2.0 and 2.5 M NaCl at 25°C and pH 7.0.At concentrations of dissolved inorganic carbon saturating for photosynthesis (200 M) gross O₂ evolution and net O₂ evolution increased with increasing salinity as well as with photon fluence rate. Light compensation was also enhanced with increased salinities. Light saturation of net O₂ evolution was reached at about 1000 mol m^-2s^-1 for all salt concentrations tested. Gross O₂ uptake in the light was increased in relation to the NaCl concentration but it was decreased with increasing photon fluence rate for almost all salinities, although an enhanced flow of light generated electrons was simultaneously observed. In addition, a comparison between gross O₂ uptake at 1000 mol photons m^-2s^-1, dark respiration before illumination and immediately after darkening of each experiment showed that gross O₂ uptake in the light paralleled but was lower than mitochondrial O₂ consumption in the dark.From these results it is suggested that O₂ uptake by Dunaliella tertiolecta in the light is mainly influenced by mitochondrial O₂ uptake. Therefore, it appears that the light dependent inhibition of gross O₂ uptake is caused by a reduction in mitochondrial O₂ consumption by light.Abbreviations DCMU 3-(3, 4-dichlorophenyl)-1, 1-dimethylurea - DHAP dihydroxy-acetonephosphate - DIC dissolved inorganic carbon - DR_a rate of dark respiration immediately after illumination - DR_b rate of dark respiration before illumination - E₀ rate of gross oxygen evolution in the light - NET rate of net oxygen evolution in the light - PFR photon fluence rate - RubP rubulose-1,5-bisphosphate - SHAM salicyl hydroxamic acid - U₀ rate of gross oxygen uptake in the light     

Leaf photosynthetic characteristics of seedlings of actinorhizal Alnus spp. and Elaeagnus spp.

Single leaf photosynthetic characteristics of Alnus glutinosa, A. incana, A. rubra, Elaeagnus angustifolia, and E. umbellata seedlings conditioned to ambient sunlight in a glasshouse were assessed. Light saturation occurred between 930 and 1400 mol m^-2s^-1 PAR for all species. Maximum rates of net photosynthesis (Pn) measured at 25°C ranged from 12.8 to 17.3 mol CO₂m^-2s^-1 and rates of dark respiration ranged from 0.74 to 0.95 mol CO₂m^-2s^-1. These values of leaf photosynthetic variables are typical of early to midsuccessional species. The rate of Pn measured at optimal temperature (20°C) and 530mol m^-2s^-1 PAR was significantly (p<0.01) correlated with leaf nitrogen concentration (r=0.69) and negatively correlated with the mean area of a leaf (r=–0.64). We suggest that the high leaf nitrogen concentration and rate of Pn observed for Elaeagnus umbellata and to a lesser degree for E. angustifolia are genetic adaptations related to their crown architecture.Abbreviations Pn net photosynthesis     

The effect of carbon dioxide concentration on respiration of growing and mature soybean leaves

Soybean plants were grown continuously at 350 and 700cm³m^?3 CO₂ at constant temperature. Respiration rates of third trifoliolate leaves were measured at the growth CO₂ concentration for the whole dark period from 5d before through to 5d after full area expansion. The short-term response of respiration rate to the measurement CO₂ concentration was also determined at each age. Respiration rates per unit of dry mass declined with age and were significantly less at a given age or RGR in leaves grown and measured at the elevated CO₂. The difference in respiration rate was largest in mature leaves and resulted from the different measurement CO₂ concentrations. The respiratory costs of the tissue synthesis, estimated from the elemental composition of the tissue, did not differ substantially between CO₂ treatments. The response of respiration rate to carbon dioxide concentration was not strongly affected by the form of nitrogen supplied. Maintenance respiration calculated by subtracting growth respiration from total respiration was negative in rapidly growing leaves for both CO₂ treatments. This indicates that CO₂ efflux in the dark does not accurately reflect the average 24 h rate of energy expenditure on growth and maintenance for soybean leaves.     

The effect of different night conditions on the CO2 fixation in a lichen Xanthoria parietina

CO₂ fixation was studied in a lichen, Xanthoria parietina, kept in continuous light, and with cyclic changes in light intensity, dark period or temperature. The diurnal and seasonal courses of CO₂ exchange were followed. The rate of net photosynthesis was observed to fall from morning to evening, and this decline was more pronounced in winter than in summer. The maximal net photosynthetic rate, 223 ng CO₂g^-1dws^-1, occured in winter and the minimum, 94 ng CO₂g^-1dws^-1, late in spring. The light compensation point in summer was four times as high as in winter. In continuous light (180 or 90 mol photons m^-2s^-1, 15°C) net photosynthesis decreased noticeably during one week, falling below the level maintained in a 12 h light: 12 h dark cycle. Photosynthetic activity did not decrease, however, in lichens held in continuous light (90 mol photons m^-2s^-1) with cyclic changes of temperature (12 h 20 °C: 12 h 5 °C). Active photosynthesis was also maintained in light of cyclically changing intensity (12 h: 12 h, 15 °C) when night-time light was at least 75% lower than illumination by day. A dark period of 4 hours in a 24-h light:dark cycle was sufficient to keep CO₂ fixation at the control level. It seems that plants need an unproductive period during the day to survive and this can be induced by fluctuations in light and/or temperature.     

On the 13C/12C isotopic signal of day and night respiration at the mesocosm level

While there is currently intense effort to examine the ¹³C signal of CO₂ evolved in the dark, less is known on the isotope composition of day‐respired CO₂. This lack of knowledge stems from technical difficulties to measure the pure respiratory isotopic signal: day respiration is mixed up with photorespiration, and there is no obvious way to separate photosynthetic fractionation (pure c_i/c_a effect) from respiratory effect (production of CO₂ with a different δ¹³C value from that of net‐fixed CO₂) at the ecosystem level. Here, we took advantage of new simple equations, and applied them to sunflower canopies grown under low and high [CO₂]. We show that whole mesocosm‐respired CO₂ is slightly ¹³C depleted in the light at the mesocosm level (by 0.2–0.8‰), while it is slightly ¹³C enriched in darkness (by 1.5–3.2‰). The turnover of the respiratory carbon pool after labelling appears similar in the light and in the dark, and accordingly, a hierarchical clustering analysis shows a close correlation between the ¹³C abundance in day‐ and night‐evolved CO₂. We conclude that the carbon source for respiration is similar in the dark and in the light, but the metabolic pathways associated with CO₂ production may change, thereby explaining the different ¹²C/¹³C respiratory fractionations in the light and in the dark.     

Photosynthetic and respiratory characterization of field grown tomato

The photosynthetic responses of tomato (Lycopersicum esculentum Mill.) leaves to environmental and ontogenetic factors were determined on plants grown in the field under high radiation and high nitrogen fertilization. Response curves showed net photosynthesis to only approach light saturation at a photosynthetic photon flux density (PPFD) of 2200 mol m^-2 s^-1, with rates of approx. 40 mol CO₂ m^-2 s^-1. A broad temperature optimum was observed between 25° and 35°C, with 50% of the photosynthetic rates remaining even at 47°C. The high rate, the lack of saturation at the equivalent of full sunlight, and the tolerance to high temperature of tomato were unusual in light of the literature on this C₃ species. Apparently, acclimation to the field environment of high radiation and hot daytime temperature, coupled with the high nitrogen nutrition, made possible the high photosynthetic performance normally associated with C₄ species.Photosynthetic ability of the leaf reached a maximum near the time of its full expansion and declined steadily thereafter, regardless of the time of leaf initiation. Leaf nitrogen content showed a similar decline with leaf ontogeny. Photosynthesis was linearly correlated with nitrogen content, whether the nitrogen variation was due to leaf age or rates of nitrogen fertilization. Internal CO₂ concentrations (C_i) of the leaf indicated that stomatal function was well coordinated with photosynthetic capacity as leaf age and fluence rate varied down to a PPFD of 500 mol m^-2 s^-1. As PPFD decreased further, there was less stomatal control and C_i increased to as high as 320 bar bar^-1.Dark respiration was highest for expanding leaves and increased nearly exponentially with temperature. Respiration was also highest for young and expanding fruits, and next highest for fruits just turning pink. Fruit respiration increased approximately linearly with temperature, and was estimated to be an important component of the CO₂ flux of the plant near maturity because of the heavy fruit load and low leaf photosynthesis at that time. The results are significant for model simulation of tomato productivity in the field.     

Non-phototrophic CO 2 fixation by soil microorganisms

Although soils are generally known to be a net source of CO₂ due to microbial respiration, CO₂ fixation may also be an important process. The non-phototrophic fixation of CO₂ was investigated in a tracer experiment with ¹⁴CO₂ in order to obtain information about the extent and the mechanisms of this process. Soils were incubated for up to 91 days in the dark. In three independent incubation experiments, a significant transfer of radioactivity from ¹⁴CO₂ to soil organic matter was observed. The process was related to microbial activity and could be enhanced by the addition of readily available substrates such as acetate. CO₂ fixation exhibited biphasic kinetics and was linearly related to respiration during the first phase of incubation (about 20–40 days). The fixation amounted to 3–5% of the net respiration. After this phase, the CO₂ fixation decreased to 1–2% of the respiration. The amount of carbon fixed by an agricultural soil corresponded to 0.05% of the organic carbon present in the soil at the beginning of the experiment, and virtually all of the fixed CO₂ was converted to organic compounds. Many autotrophic and heterotrophic biochemical processes result in the fixation of CO₂. However, the enhancement of the fixation by addition of readily available substrates and the linear correlation with respiration suggested that the process is mainly driven by aerobic heterotrophic microorganisms. We conclude that heterotrophic CO₂ fixation represents a significant factor of microbial activity in soils.     

Acclimation of respiration to temperature and CO2 in seedlings of boreal tree species in relation to plant size and relative growth rate

The role of acclimation of dark respiration to temperature and CO₂ concentration and its relationship to growth are critical in determining plant response to predicted global change. We explored temperature acclimation of respiration in seedlings of tree species of the North American boreal forest. Populus tremuloides, Betula papyrifera, Larix laricina, Pinus banksiana, and Picea mariana plants were grown from seed in controlled-environments at current and elevated concentrations of CO₂ (370 and 580 μmol mol^–1) in combination with three temperature treatments of 18/12, 24/18, and 30/24 °C (light/dark period). Specific respiration rates of roots and shoots acclimated to temperature, damping increases in rates across growth-temperature environments compared to short-term temperature responses. Compared at a standard temperature, root and shoot respiration rates were, on average, 40% lower in plants grown at the highest compared to lowest growth temperature. Broad-leaved species had a lower degree of temperature acclimation of respiration than did the conifers. Among species and treatment combinations, rates of respiration were linearly related to size and relative growth rate, and relationships were comparable among growth environments. Specific respiration rates and whole-plant respiratory CO₂ efflux as a proportion of daily net CO₂ uptake increased at higher growth temperatures, but were minimally affected by CO₂ concentration. Whole-plant specific respiration rates were two to three times higher in broad-leaved than coniferous species. However, compared to faster-growing broad-leaved species, slower-growing conifers lost a larger proportion of net daily CO₂ uptake as respiratory CO₂ efflux, especially in roots. Interspecific variation in acclimation responses of dark respiration to temperature is more important than acclimation of respiration to CO₂ enrichment in modifying tree seedling growth responses to projected increases in CO₂ concentration and temperature.