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.     

Stem respiration of ponderosa pines grown in contrasting climates: implications for global climate change

We examined the effects of climate and allocation patterns on stem respiration in ponderosa pine (Pinus ponderosa) growing on identical substrate in the cool, moist Sierra Nevada mountains and the warm, dry, Great Basin Desert. These environments are representative of current climatic conditions and those predicted to accompany a doubling of atmospheric CO₂, respectively, throughout the range of many western north American conifers. A previous study found that trees growing in the desert allocate proportionally more biomass to sapwood and less to leaf area than montane trees. We tested the hypothesis that respiration rates of sapwood are lower in desert trees than in montane trees due to reduced stem maintenance respiration (physiological acclimation) or reduced construction cost of stem tissue (structural acclimation). Maintenance respiration per unit sapwood volume at 15°C did not differ between populations (desert: 6.39 ± 1.14 SE μmol m⁻³ s⁻¹, montane: 6.54 ± 1.13 SE μmol m⁻³ s⁻¹, P = 0.71) and declined with increasing stem diameter (P = 0.001). The temperature coefficient of respiration (Q ₁₀) varied seasonally within both environments (P = 0.05). Construction cost of stem sapwood was the same in both environments (desert: 1.46 ± 0.009 SE g glucose g⁻¹ sapwood, montane: 1.48 ± 0.009 SE glucose g⁻¹ sapwood, P = 0.14). Annual construction respiration calculated from construction cost, percent carbon and relative growth rate was greater in montane populations due to higher growth rates. These data provide no evidence of respiratory acclimation by desert trees. Estimated yearly stem maintenance respiration was greater in large desert trees than in large montane trees because of higher temperatures in the desert and because of increased allocation of biomass to sapwood. By analogy, these data suggest that under predicted increases in temperature and aridity, potential increases in aboveground carbon gain due to enhanced photosynthetic rates may be partially offset by increases in maintenance respiration in large trees growing in CO₂-enriched atmospheres. Received: 4 November 1996 / Accepted: 23 January 1997     

Ecosystem respiration depends strongly on photosynthesis in a temperate heath

We measured net ecosystem CO₂ flux (F _n) and ecosystem respiration (R _E), and estimated gross ecosystem photosynthesis (P _g) by difference, for two years in a temperate heath ecosystem using a chamber method. The exchange rates of carbon were high and of similar magnitude as for productive forest ecosystems with a net ecosystem carbon gain during the second year of 293 ± 11 g C m⁻² year⁻¹ showing that the carbon sink strength of heather-dominated ecosystems may be considerable when C. vulgaris is in the building phase of its life cycle. The estimated gross ecosystem photosynthesis and ecosystem respiration from October to March was 22% and 30% of annual flux, respectively, suggesting that both cold-season carbon gain and loss were important in the annual carbon cycle of the ecosystem. Model fit of R _E of a classic, first-order exponential equation related to temperature (second year; R ² = 0.65) was improved when the P _g rate was incorporated into the model (second year; R ² = 0.79), suggesting that daytime R _E increased with increasing photosynthesis. Furthermore, the temperature sensitivity of R _E decreased from apparent Q ₁₀ values of 3.3 to 3.9 by the classic equation to a more realistic Q ₁₀ of 2.5 by the modified model. The model introduces R _photo, which describes the part of respiration being tightly coupled to the photosynthetic rate. It makes up 5% of the assimilated carbon dioxide flux at 0°C and 35% at 20°C implying a high sensitivity of respiration to photosynthesis during summer. The simple model provides an easily applied, non-intrusive tool for investigating seasonal trends in the relationship between ecosystem carbon sequestration and respiration.     

Dynamics of soil respiration in sparse <Emphasis Type="Italic">Ulmus pumila</Emphasis> woodland under semi-arid climate

Sparse Ulmus pumila woodlands play an important role in contributing to ecosystem function in semi-arid grassland of northern China. To understand the key attributes of soil carbon cycling in U. pumila woodland, we studied dynamics of soil respiration in the canopy field (i.e., the projected crown cover area) and the open field at locations differing in distance (i.e., at 1–1.5, 3–4, 10, and >15 m) to tree stems from July through September of 2005, and measured soil biotic factors (e.g., fine root mass, soil microbial biomass, and activity) and abiotic factors [e.g., soil water content (SWC) and organic carbon] in mid-August. Soil respiration was further separated into root component and microbial component at the end of the field measurement in September. Results showed that soil respiration had a significant exponent relationship with soil temperature at 10-cm depth. The temperature sensitivity index of soil respiration, Q ₁₀, was lower than the global average of 2.0, and declined significantly (P < 0.05) with distance. The rate of soil respiration was generally greater in the canopy field than in the open field; monthly mean of soil respiration was 305.5–730.8 mg CO₂ m⁻² h⁻¹ in the canopy field and 299.6–443.1 mg CO₂ m⁻² h⁻¹ in the open field from July through September; basal soil respiration at 10°C declined with distance, and varied from ~250 mg CO₂ m⁻² h⁻¹ near tree stems to <200 mg CO₂ m⁻² h⁻¹ in the open field. Variations in soil respiration with distance were consistent with patterns of SWC, fine root mass, microbial biomass and activities. Regression analysis indicated that soil respiration was tightly coupled with microbial respiration and only weakly related to root respiration. Overall, variations in SWC, soil nutrients, microbial biomass, and microbial activity are largely responsible for the spatial heterogeneity of soil respiration in this semi-arid U. pumila woodland.     

Estimation of carbon storage, carbon inputs, and soil CO2 efflux of alder plantations on granite soil in central Korea: comparison with Japanese larch plantation

Alder is a typical species used for forest rehabilitation after disturbances because of its N₂-fixing activities through microbes. To investigate forest dynamics of the carbon budget, we determined the aboveground and soil carbon content, carbon input by litterfall to belowground, and soil CO₂ efflux over 2 years in 38-year-old alder plantations in central Korea. The estimated aboveground carbon storage and increment were 47.39 Mg C ha⁻¹ and 2.17 Mg C ha⁻¹ year⁻¹. Carbon storage in the organic layer and in mineral soil in the topsoil to 30 cm depth were, respectively, 3.21 and 66.85 Mg C ha⁻¹. Annual carbon input by leaves and total litter in the study stand were, respectively, 1.78 and 2.68 Mg C ha⁻¹ year⁻¹. The aboveground carbon increment at this stand was similar to the annual carbon inputs by total litterfall. The diurnal pattern of soil CO₂ efflux was significantly different in May, August, and October, typically varying approximately twofold throughout the course of a day. In the seasonally observed pattern, soil CO₂ efflux varied strongly with soil temperature; increasing trends were evident during the early growing season, with sustained high rates from mid May through late October. Soil CO₂ efflux was related exponentially to soil temperature (R ² = 0.85, P < 0.0001), but not to soil water content. The Q ₁₀ value for this plantation was 3.8, and annual soil respiration was estimated at 10.2 Mg C ha⁻¹ year⁻¹. An erratum to this article can be found at     

Changes in soil CO2 and O2 concentrations when radiata pine is grown in competition with pasture or weeds and possible feedbacks with radiata pine root growth and respiration

This study examined the reciprocal effects of growing ryegrass, lotus and other weed species in competition with radiata pine on soil CO₂ and O₂ concentrations and on the growth and root respiration of the radiata pine. Soil O₂ concentrations decreased and soil CO₂ concentrations increased with increasing soil depth. Radiata pine plus competing species slightly reduced soil O₂ concentrations and markedly increased soil CO₂ concentrations (up to 40 mmol mol⁻¹) compared with radiata pine alone. The dry weights of shoots and roots, and the root respiration rates of radiata pine grown with competing vegetation were much less than those for radiata pine alone. This probably was not solely caused by competition for nutrients water or light since adequate water and nutrients were supplied to all treatments and the radiata pine overtopped the competing vegetation. When radiata pine roots were raised in NaHCO₃ solutions equivalent to a range of CO₂ concentrations, succinate dehydrogenase activity (a metabolic indicator of mitochondrial respiration) and elongation rates of roots decreased as CO₂ concentrations increased from 0 to 40 mmol mol⁻¹. This suggests that the elevated CO₂ concentrations found in the experiments in soil was the cause, at least in part, of the reduced growth of radiata pine in competition with other species. This revised version was published online in June 2006 with corrections to the Cover Date.     

Soil O2 and CO2 effects on root respiration of cacti

Through use of a recently developed technique that can measure CO₂ exchange by individual attached roots, the influences of soil O₂ and CO₂ concentrations on root respiration were determined for two species of shallow-rooted cacti that typically occur in porous, well-drained soils. Although soil O₂ concentrations in the rooting zone in the field were indistinguishable from that in the ambient air (21% by volume), the CO₂ concentrations 10 cm below the soil surface averaged 540 μLL⁻¹ for the barrel cactusFerocactus acanthodes under dry conditions and 2400 μLL⁻¹ under wet conditions in a loamy sand. For the widely cultivated platyopuntiaOpuntia ficus-indica in a sandy clay loam, the CO₂ concentration at 10 cm averaged 1080 μLL⁻¹ under dry conditions and 4170 μLL⁻¹ under wet conditions. For both species, the respiration rate in the laboratory was zero at 0% O₂ and increased to its maximum value at 5% O₂ for rain roots (roots induced by watering) and 16% O₂ for established roots. Established roots ofO. ficus-indica were slightly more tolerant of elevated CO₂ than were those ofF. acanthodes, 5000 μLL⁻¹ inhibiting respiration by 35% and 46%, respectively. For both species, root respiration was reduced to zero at 20,000 μLL⁻¹ (2%) CO₂. In contrast to the reversible effects of 0% O₂, inhibition by 2% CO₂ was irreversible and led to the death of cortical cells in established roots in 6 h. Although the restriction of various cacti and other CAM plants to porous soils has generally been attributed to their requirement for high O₂ concentrations, the present results indicate that susceptibility of root respiration to elevated soil CO₂ concentrations may be more important.     

Canopy photosynthetic production in a Japanese larch stand. I. Seasonal and vertical changes of leaf characteristics along the light gradient in a canopy

In an 18 year old Japanese larch stand, leaf characteristics such as area, weight, gross photosynthetic rate and respiration rate were studied in order to obtain basic information on estimating canopy photosynthesis and respiration. The leaf growth courses in area and weight from bud opening were approximated by simple logistic curves. The growth coefficient for the area growth curve was 0.155–0.175 day⁻¹, while that for the weight growth was 0.112–0.117 day⁻¹. The larger growth coefficient in area growth caused the seasonal change in specific leaf area (SLA) that increased after bud opening to its peak early in May at almost 300 cm² g⁻¹ and then decreased until it leveled off at about 140 cm²g⁻¹. The change inSLA indicates the possibility that leaf area growth precedes leaf thickness growth. The relationship between the coefficientsa andb of the gross photosynthetic rate (p)-light flux density (1) curve (p=bI/(1+aI)) and the mean relative light flux density (I′/I ₀) at each canopy height were approximated by hyperbolic formulae:a=A/(I′/I ₀)+B andb=C/(I′/I ₀)+D. Leaf respiration rate was also increased with increasingI′/I ₀. Seasonal change of gross photosynthetic rate and leaf respiration rate were related to mean air temperature through linear regression on semilogarithmic co-ordinates.     

An estimation of CO<Subscript>2</Subscript> fixation capacity in mangrove forest using two methods of CO<Subscript>2</Subscript> gas exchange and growth curve analysis

In many coastal areas of South-East Asia, attempts have been made to revive coastal ecosystem by initiating projects that encourage planting of mangrove trees. Compared to the terrestrial trees, mangrove trees possess a higher carbon fixation capacity. It becomes a very significant option for clean development mechanism (CDM) program. However, a reliable method to estimate CO₂ fixation capacity of mangrove trees has not been established. Acknowledging the above fact, we decided to set up an estimation method for the CDM program, using gas exchange analysis to estimate mangrove productivity, we put into consideration the net CO₂ fixation of reforested Kandelia candel (5-, 10-, and 15-year-old stand). This was estimated by gas exchange analysis and growth curve analysis. In growth curve analysis, we drew a growth curve of a single stand using data of above- and below-ground biomass. In the gas exchange analysis, we calculated CO₂ fixation capacity by (1) measuring respiration rate of each organ of stand and calculating respiratory CO₂ emission from above- to below-ground biomass. (2) Measuring the single-leaf photosynthetic rate in response to light intensity and calculating the photosynthetic CO₂ absorption. (3) We also developed a model for the diurnal changes in temperature, and monthly averages based on one-day estimation of CO₂ absorption and emission, which we corrected by this model in order to estimate the net CO₂ fixation capacity in response to temperature. Comparing the biomass accumulation of the two methods constructed for the same forest, the above-ground biomass accumulation of 10-year-old forest (34.3 ton ha⁻¹ yr⁻¹) estimated by gas exchange analysis was closely compared to those of growth curve analysis (26.6 ton ha⁻¹ yr⁻¹), suggesting that the gas exchange analysis was capable of estimating mangrove productivity. The validity of the estimated CO₂ fixation capacity by the gas exchange analysis and the growth curve analysis was also discussed.     

Seasonal, daily and diurnal variations in the stable carbon isotope composition of carbon dioxide respired by tree trunks in a deciduous oak forest

The stable C isotope composition (δ¹³C) of CO₂ respired by trunks was examined in a mature temperate deciduous oak forest (Quercus petraea). Month-to-month, day-to-day and diurnal, measurements were made to determine the range of variations at different temporal scales. Trunk growth and respiration rates were assessed. Phloem tissue was sampled and was analysed for total organic matter and soluble sugar ¹³C composition. The CO₂ respired by trunk was always enriched in ¹³C relative to the total organic matter, sometimes by as much as 5‰. The δ¹³C of respired CO₂ exhibited a large seasonal variation (3.3‰), with a relative maximum at the beginning of the growth period. The lowest values occurred in summer when the respiration rates were maximal. After the cessation of radial trunk growth, the respired CO₂ δ¹³C values showed a progressive increase, which was linked to a parallel increase in soluble sugar content in the phloem tissue (R = 0.95; P < 0.01). At the same time, the respiration rates declined. This limited use of the substrate pool might allow the discrimination during respiration to be more strongly expressed. The late-season increase in CO₂ δ¹³C might also be linked to a shift from recently assimilated C to reserves. At the seasonal scale, CO₂ δ¹³C was negatively correlated with air temperature (R = −0.80; P < 0.01). The diurnal variation sometimes reached 3‰, but the range and the pattern depended on the period within the growing season. Contrary to expectations, diurnal variations were maximal in winter and spring when the leaves were missing or not totally functional. By contrast to the seasonal scale, these diurnal variations were not related to air temperature or sugar content. Our study shows that seasonal and diurnal variations of respired ¹³C exhibited a similar large range but were probably explained by different mechanisms.     

Relationship between net photosynthesis and leaf respiration in Mediterranean evergreen species

The relationship between net photosynthetic (P _N) and leaf respiration (R) rates of Quercus ilex, Phillyrea latifolia, Myrtus communis, Arbutus unedo, and Cistus incanus was monitored in the period February 2006 to February 2007. The species investigated had low R and P _N during winter, increasing from March to May, when mean air temperature reached 19.2 °C. During the favourable period, C. incanus and A. unedo had a higher mean P _N (16.4±2.4 μmol m⁻² s⁻¹) than P. latifolia, Q. ilex, and M. communis (10.0±1.3 μmol m⁻² s⁻¹). The highest R (1.89±0.30 μmol m⁻² s⁻¹, mean of the species), associated to a significant P _N decrease (62 % of the maximum, mean value of the species), was measured in July (mean R/P _N ratio 0.447±0.091). Q₁₀, indicating the respiration sensitivity to short-term temperature increase, was in the range 1.49 to 2.21. Global change might modify R/P _N determining differences in dry matter accumulation among the species, and Q. ilex and P. latifolia might be the most favoured species by their ability to maintain sufficiently higher P _N and lower R during stress periods.     

北京典型树种木质组织碳释放速率温度敏感性的时间变化规律和铅锤分异特征

采用红外气体分析法(IRGA)于2014年1—12月原位测定了北京市4个典型树种(国槐Sophora japonica,旱柳Salix matsudana,华北落叶松Larix principis-rupprechtii和侧柏Platycladus orientalis)在不同高度上的木质组织CO_2通量速率(E_(CO_2)),旨在比较不同树种间E_(CO_2)及其温度敏感性(Q_(10))的时间变化规律和铅锤分异特征。研究结果显示:(1)4个树种的E_(CO_2)均表现为单峰型季节变化规律,生长月份内的E_(CO_2)显著高于非生长月份,温度和枝干的径向生长是影响E_(CO_2)季节变化的主要因素;(2)E_(CO_2)对温度的敏感性在夏季月份明显降低,且出现明显的垂直分异:Q_(10)随测量高度的增加而增加,呈现出非连续的阶梯分布;(3)在日间尺度上,阔叶树种E_(CO_2)对温度的感性系数Q_(10)出现昼夜不对称现象,晚上Q_(10)明显升高。准确量化E_(CO_2)的时间变化规律和铅锤分异特征,细化不同时间尺度下E_(CO_2)对温度的响应特征,成为准确估算木质组织碳排放的前提条件。     

Soil respiration of Alaskan tundra at elevated atmospheric carbon dioxide concentrations

Summary CO₂ efflux from tussock tundra in Alaska that had been exposed to elevated CO₂ for 2.5 growing seasons was measured to assess the effect of long- and short-term CO₂ enrichment on soil respiration. Long-term treatments were: 348, 514, and 683 μll⁻¹ CO₂ and 680 μll⁻¹ CO₂+4°C above ambient. Measurements were made at 5 CO₂ concentrations between 87 and 680 μll⁻¹ CO₂. Neither long- or short-term CO₂ enrichment significantly affected soil CO₂ efflux. Tundra developed at elevated temperature and 680 μll⁻¹ CO₂ had slightly higher, but not statistically different, mean respiration rates compared to untreated tundra and to tundra under CO₂ control alone.     

Chlorophyll fluorescence imaging of photosynthetic activity in sun and shade leaves of trees

The differences in pigment levels, photosynthetic activity and the chlorophyll fluorescence decrease ratio R _Fd (as indicator of photosynthetic rates) of green sun and shade leaves of three broadleaf trees (Platanus acerifolia Willd., Populus alba L., Tilia cordata Mill.) were compared. Sun leaves were characterized by higher levels of total chlorophylls a + b and total carotenoids x + c as well as higher values for the weight ratio chlorophyll (Chl) a/b (sun leaves 3.23–3.45; shade leaves: 2.74–2.81), and lower values for the ratio chlorophylls to carotenoids (a + b)/(x + c) (with 4.44–4.70 in sun leaves and 5.04–5.72 in shade leaves). Sun leaves exhibited higher photosynthetic rates P _N on a leaf area basis (mean of 9.1–10.1 μmol CO₂ m⁻² s⁻¹) and Chl basis, which correlated well with the higher values of stomatal conductance G _s (range 105–180 mmol m⁻² s⁻¹), as compared to shade leaves (G _s range 25–77 mmol m⁻² s⁻¹; P _N: 3.2–3.7 μmol CO₂ m⁻² s⁻¹). The higher photosynthetic rates could also be detected via imaging the Chl fluorescence decrease ratio R _Fd, which possessed higher values in sun leaves (2.8–3.0) as compared to shade leaves (1.4–1.8). In addition, via R _Fd images it was shown that the photosynthetic activity of the leaves of all trees exhibits a large heterogeneity across the leaf area, and in general to a higher extent in sun leaves than in shade leaves.     

毛白杨树干呼吸及其温度敏感性季节变化特征

树干呼吸(E_s)是森林生态系统碳循环过程的重要组成部分,深入理解树干呼吸过程对未来气候变暖的响应及反馈机制有助于更加精确地估算森林生态系统碳储量。为揭示毛白杨树干呼吸及其温度敏感性的昼夜变化和季节动态规律,利用Li-Cor6400便携式光合作用测定系统及其配套使用的土壤呼吸测量气室(LI-6400-09)对冀南平原区毛白杨的树干呼吸和树干温度实施为期1年的连续监测。结果表明:(1)在生长季,毛白杨树干呼吸与树干温度之间在晚上呈现正相关的关系(R~2=0.88);相反,两者在白天为负相关的关系(R~2=0.96)。(2)整个观测期内,毛白杨树干呼吸和树干温度均呈现"钟形"的变化曲线,树干呼吸与树干温度之间存在着较好的指数函数关系(R~2=0.93),且树干呼吸的温度敏感性系数(Q_(10))为2.62;不同季节毛白杨树干呼吸的Q_(10)存在差异,生长季的Q_(10)(1.95)明显低于非生长季(3.00),表明生长呼吸和维持呼吸对温度的响应也并不相同。(3)温度矫正后的毛白杨树干呼吸(R_(15))在昼夜和季节尺度上均存在明显的变异,即夜晚的R_(15)显著高于白天(P0.01),生长季的R_(15)明显高于非生长季(P0.05);树干可溶性糖含量与生长季的R_(15)存在较好的相关性(R~2=0.52),而非生长季的R_(15)却主要受到树干淀粉含量的影响。研究结果表明,在生长季,毛白杨树干呼吸的在日变化主要受到温度的影响,而在季节尺度上Q_(10)的变异则与树干呼吸中维持呼吸所占比例及树干中非结构性碳水化合物(可溶性糖和淀粉)的含量及类型紧密相关。     

Cyclic carbon dioxide release in the dampwood termite, Zootermopsis nevadensis (Hagen)

Real-time traces of CO₂ release of pseudergates of the dampwood termite, Zootermopsis nevadensis (Hagen) were obtained using flow-through respirometry. Traces were made at each of six temperatures, between 10 and 35°C. Termites released CO₂ in a cyclic pattern at each of the six temperatures. CO₂ release rate (as in ml h⁻¹) increased significantly with temperature and body mass. Rate of change in with temperature (or Q₁₀) was 2.11. Degree of cycling in CO₂ traces was estimable using the coefficient of variability. Coefficient of variability for both acyclic and cyclic traces declined exponentially with increasing temperature.     

Respiration for maintenance and growth inReynoutria japonica ecotypes from different altitudes on Mt Fuji

Respiration for maintenance and growth ofReynoutria japonica ecotypes from altitudes of 700 and 2420 m on Mt Fuji were measured in two controlled thermal conditions. The maintenance respiration of the high-altitude ecotype at both 15 and 25°C was significantly (1.7-fold) higher than that of the low-altitude ecotype, whereas growth respiration was independent of both ecotype and temperature. The temperature coefficient (Q₁₀) of the maintenance respiration was about 1.9 in both ecotypes. The results show that there is ecotypic differentiation in the performance of maintenance respiration. It is suggested that the high maintenance respiration of the high-altitudeR. japonica ecotype is advantageous in severe upland environments but disadvantageous in a warm lowland climate in terms of carbon economy.     

Long-Term Effects of Elevated CO2 on Woody Tissues Respiration of Norway Spruce Studied in Open-Top Chambers

In an open-top chamber experiment located in a mountain stand of 14-years-old Norway spruce (Picea abies [L.] Karst.), trees were continuously exposed to either ambient CO₂ concentration (A), or ambient + 350 µmol mol^–1 (E) over four growing seasons. Respiration rates of different woody parts (stem, branches, coarse roots) were measured during the last growing season. The calculated increase in the respiration rate related to a 10 °C temperature change (Q₁₀) was different in stem compared to branches and roots. Differences between the E and A variants were statistically significant only for roots in the autumn. Stem maintenance respiration (R_Ms) measured in April and November (periods of no growth activity) were not different. The stem respiration values (R_s) were recalculated to a standard temperature of 15 °C to estimate the seasonal course. The obtained R_s differed significantly between used variants during July and August. At the end of the season, R_s in E decreased slower than in A, indicating some prolongation of the physiological activity under the elevated CO₂ concentration. The total stem respiration carbon losses for the investigated growing season (May – September) were higher for A (2.32 kg(C) m^–2 season^–1) compared to E (2.12 kg(C) m^–2 season^–1). The respiration rates of the whorl branches (R_b) were lower compared with the stem respiration but not significantly different between the used variants. The root respiration rate was increased in E variant.     

Whole plant respiration and photosynthesis of wheat under increased CO2 concentration and temperature: long-term vs. short-term distinctions for modelling

Short- and long-term effects of elevated CO₂ concentration and temperature on whole plant respiratory relationships are examined for wheat grown at four constant temperatures and at two CO₂ concentrations. Whole plant CO₂ exchange was measured on a 24 h basis and measurement conditions varied both to observe short-term effects and to determine the growth respiration coefficient (r_g), dry weight maintenance coefficient (r_m), basal (i.e. dark acclimated) respiration coefficient (r_g), and 24 h respiration:photosynthesis ratio (R:P). There was no response of r_g to short-term variation in CO2 concentration. For plants with adequate N supply, r_g was unaffected by the growth-CO₂ despite a 10% reduction in the plant's N concentration (%N). However, r_m was decreased 13%, and r_b was decreased 20% by growth in elevated CO₂ concentration relative to ambient. Nevertheless, R:P was not affected by growth in elevated CO₂. Whole plant respiration responded to short-term variation of ± 5 °C around the growth temperature with low sensitivity (Q₁₀= 1.8 at 15 °C, 1.3 at 30 °C). The shape of the response of whole plant respiration to growth temperature was different from that of the short term response, being a slanted S-shape declining between 25 and 30 °C. While r_m, increased, r_g decreased when growth temperature increased between 15 and 20 °C. Above 20 °C r_m became temperature insensitive while r_g increased with growth temperature. Despite these complex component responses, R:P increased only from 0.40 to 0.43 between 15° and 30 °C growth temperatures. Giving the plants a step increase in temperature caused a transient increase in R:P which recovered to the pre-transient value in 3 days. It is concluded that use of a constant R:P with respect to average temperature and CO₂ concentration may be a more simple and accurate way to model the responses of wheat crop respiration to ‘climate change’ than the more complex and mechanistically dubious functional analysis into growth and maintenance components.     

Stomatal conductance and not stomatal density determines the long-term reduction in leaf transpiration of poplar in elevated CO<Subscript>2</Subscript>

Using a free-air CO₂ enrichment (FACE) experiment, poplar trees (Populus × euramericana clone I214) were exposed to either ambient or elevated [CO₂] from planting, for a 5-year period during canopy development, closure, coppice and re-growth. In each year, measurements were taken of stomatal density (SD, number mm⁻²) and stomatal index (SI, the proportion of epidermal cells forming stomata). In year 5, measurements were also taken of leaf stomatal conductance (g _s, μmol m⁻² s⁻¹), photosynthetic CO₂ fixation (A, mmol m⁻² s⁻¹), instantaneous water-use efficiency (A/E) and the ratio of intercellular to atmospheric CO₂ (C_i:C_a). Elevated [CO₂] caused reductions in SI in the first year, and in SD in the first 2 years, when the canopy was largely open. In following years, when the canopy had closed, elevated [CO₂] had no detectable effects on stomatal numbers or index. In contrast, even after 5 years of exposure to elevated [CO₂], g _s was reduced, A/E was stimulated, and C_i:C_a was reduced relative to ambient [CO₂]. These outcomes from the long-term realistic field conditions of this forest FACE experiment suggest that stomatal numbers (SD and SI) had no role in determining the improved instantaneous leaf-level efficiency of water use under elevated [CO₂]. We propose that altered cuticular development during canopy closure may partially explain the changing response of stomata to elevated [CO₂], although the mechanism for this remains obscure.