Temporal expression of effects of varying nitrogen supply on canopy growth, photosynthesis and fruit production for Actinidia deliciosa vines in the field

The effects of varying nitrogen supply on canopy leaf area, response of leaf net photosynthesis (A_n) to quantum flux density (Q), and fruit yields of kiwifruit vines (Actinidia deliciosa var. deliciosa) were examined in a two-year field experiment. Vines were grown with 0, 250 or 750 kg N ha^?1 year^?1. The responses to nitrogen supply were compared with responses to shade, to examine the impact of reduced carbon assimilation on canopy leaf area and fruit yields. Nitrogen supply did not affect significantly any of the measured variables during the first season of the experiment. In the second season, canopy leaf area was reduced significantly where nitrogen supply was limited. The quantum efficiency of photosynthesis (φ_q) increased from 0. 03 mol CO₂ mol^?1 Q soon after leaf emergence to more than 0. 05 mol CO₂ mol^?1 Q during the middle of the growing season. The quantum saturated rate of A_n (A_sat) also increased during the season, from 7–10 μmol CO₂ m^?2 s^?1 soon after leaf emergence, to 15–20 (μmol CO₂ m^?2 s^?1 during the middle of the growing season. φ_q and A_sat increased significantly with nitrogen supply at all measurement times during the second season. For vines with high nitrogen, fruit yields in both seasons were similar, averaging 3. 05 kg m^?2. Fruit yields in the second season were reduced significantly where nitrogen supply was limited, due to reduced fruit numbers. The relative effects of reduced leaf area and reduced leaf photosynthesis for carbon assimilation by nitrogen deficient vines were examined using a mathematical model of canopy photosynthesis for kiwifruit vines. Simulations of canopy photosynthesis indicated that effects on leaf area and on leaf photosynthesis were of similar importance in the overall effects of nitrogen deficiency on carbon assimilation. The effects of nitrogen supply on fruit numbers (i. e. flower development) preceded the measured effects on carbon assimilation, indicating that the nitrogen supply affected carbon partitioning to reserves in the first season.     

Foliar maintenance respiration of subalpine and boreal trees and shrubs in relation to nitrogen content

A nitrogen-based model of maintenance respiration (R_m) would link R_m with nitrogen-based photosynthesis models and enable simpler estimation of dark respiration flux from forest canopies. To test whether an N-based model of R_m would apply generally to foliage of boreal and subalpine woody plants, I measured R_m (CO₂ efflux at night from fully expanded foliage) for foliage of seven species of trees and shrubs in the northern boreal forest (near Thompson, Manitoba, Canada) and seven species in the subalpine montane forest (near Fraser, Colorado, USA). At 10°C, average R_m for boreal foliage ranged from 0.94 to 6.8μmol kg^?1 s^?1 (0.18–0.58 μmol m^?2 s^?1) and for subalpine foliage it ranged from 0.99 to 7.6 μmol kg^?1 s^?1 (0.28–0.64μmol m^?2 s^?1). CO₂ efflux at 10°C for the samples was only weakly correlated with sample weight (r = 0.11) and leaf area (r = 0.58). However, CO₂ efflux per unit foliage weight was highly correlated with foliage N concentration [r = 0.83, CO₂ flux at 10°C (mol kg^?1 s^?1) = 2.62 × foliage N (mol kg^?1)J, and slopes were statistically similar for the boreal and subalpine sites (P=0.28). CO₂ efflux per unit of foliar N was 1.8 times that reported for a variety of crop and wildland species growing in warmer climates.     

Photosynthetic rates in relation to leaf phosphorus content in pioneer versus climax tropical rainforest trees

In Guyana dense rainforest occurs on intensely weathered acid soils, low in soil phosphorus. To investigate whether low P availability limits photosynthesis of trees growing on these soils more than N does, leaf P and N content, and their relationship with the photosynthetic capacity (A _sat, mol CO₂ m^-2 s^-1) were studied for nine pioneer and climax tree species in a range of light climates. Light environment was described using hemispherical photographs. For both pioneer and climax species, leaf P content (r ²=0.71 and 0.23, respectively) is a more important determinant of A _sat than leaf N content (r ²=0.54 and 0.12, respectively). Pioneer species have a higher leaf P and N content than climax species. At similar P or N content, pioneers have a higher A _sat than climax species. The saplings studied had a relatively high A _sat, considering their low P concentration (15–30 mol P g^-1). All species studied had a constant leaf P and N concentration and photosynthetic capacity across light climates, because specific leaf mass (g m^-2) increased similarly with light availability. This acclimation to a change in light environment makes a possible limitation of A _sat by P or N independent of light environment.     

Can chilling tolerance of C4 photosynthesis in Miscanthus be transferred to sugarcane?

The goal of this study was to investigate whether chilling tolerance of C₄ photosynthesis in Miscanthus can be transferred to sugarcane by hybridization. Net leaf CO₂ uptake (A_sat) and the maximum operating efficiency of photosystem II (Ф_PSII) were measured in warm conditions (25 °C/20 °C), and then during and following a chilling treatment of 10 °C/5 °C for 11 day in controlled environment chambers. Two of three hybrids (miscanes), ‘US 84‐1058’ and ‘US 87‐1019’, did not differ significantly from the chilling tolerant M. ×giganteus ‘Illinois’ (Mxg), for A_sat, and Φ_PSII measured during chilling. For Mxg grown at 10 °C/5 °C for 11 days, A_sat was 4.4 μmol m^?2 s^?1, while for miscane ‘US 84‐1058’ and ‘US 87‐1019’, A_sat was 5.7 and 3.5 μmol m^?2 s^?1, respectively. Miscanes ‘US 84‐1058’ and ‘US 87‐1019’ and Mxg had significantly higher rates of A_sat during chilling than three tested sugarcanes. A third miscane showed lower rates than Mxg during chilling, but recovered to higher rates than sugarcane upon return to warm conditions. Chilling tolerance of ‘US 84‐1058’ was further confirmed under autumn field conditions in southern Illinois. The selected chilling tolerant miscanes have particular value for biomass feedstock and biofuel production and at the same time they can be a starting point for extending sugarcane's range to colder climates.     

Catalogo delle Alghe Raccolte Lungo IL Litorale di Trani

Abstract

Canopy light interception (CPFD_Int), spectral irradiance, leaf water potential, gas- exchange and optical properties were measured in an irrigated vineyard (Vitis vinifera L. cv Montepulciano) trained to the so-called tendone system in which leaf area index (LAI) was varied by means of 50% (T50) or 75% (T75) cluster removal. The 20.5 t ha^?1 yield in the unthinned treatment (UT) decreased by only 36% in T50 and by 52% in T75. LAI and CPFD_Int similarly increased until summer pruning when LAI was 1.75 m² m^?2 in UT, and 25.6% or 62.2% higher in T50 and T75, respectively. The two thinned treatments had only 12.4% higher CPFD_Int than in UT (1167.1 μmol m^?2 s^?1) due to the increased leaf self-shading. The red-to-far red ratio (R: FR) was as low as 0.10 below the canopy. Light-saturated CO₂ assimilation (A _max) in June averaged 14.4 μmol m^?2 s^?1 in sun-exposed leaves, and 7.6 μmol m^?2 s^?1 in shade leaves. By contrast, the apparent quantum yield of CO₂ assimilation (φ_e) was not significantly affected by leaf position, averaging 0.029 and 0.070 mol mol^?1 in June and October, respectively. Middle and low canopy leaves had only 27 or 6%, respectively, of the top canopy leaves actual CO₂ assimilation rate.     

Adaptation of epiphytic bryophytes in the understorey attributing to the correlations and trade-offs between functional traits

This study explores adaptive strategies of epiphytic bryophytes in the understorey by investigating the photosynthetic characteristics, pigment concentrations and nutrient stoichiometry, as well as other functional traits of three trunk-dwelling bryophytes in a subtropical montane cloud forest in SW China. The results showed that their light-saturated net photosynthetic rate (A_nmax?L), light saturation point (I_sat), light compensation point (I_c) and dark respiration rate (R_d) were ca 0.55, 106.72, 4.17 and 0.25?μmol?m^?2?s^?1, respectively. Furthermore, the samples demonstrated photosynthetic down-regulation under high irradiance. These photosynthetic characteristics can be explained by higher total chlorophyll concentrations, specific leaf area, chlorophyll per unit leaf N (Chl/N), lower ratio of chlorophyll a to chlorophyll b (Chl a/b) and photosynthetic nitrogen-use efficiency. We suggest that the bryophytes adapted to the shaded understorey microhabitats through a series of correlations and trade-offs between functional traits.     

Growth potential of Lemna gibba: Effect of CO2 enrichment at high photon flux rate

Lemna gibba L. was cultivated in continuous light (800–1200 μmol quanta m^?2s^?1, 320–400 W m^?2) and normal or CO₂-enriched air (1500 μl CO₂ l^?1), with a continuous nutrient supply. Increased CO₂ concentration increased the unit leaf rate (ULR) or net assimilation rate and decreased the leaf area ratio (LAR) (photosynthetic area per unit dry weight), but the relative growth rate was unchanged (0.43 g g^?1 day^?1). The changes in ULR and LAR indicate that organic matter production can be increased with CO₂ enrichment at high photon flux rate (PFR).     

Photosynthetic characteristics of Amaranthus tricolor,a C4 tropical leafy vegetable

The gas exchange characteristics are reported for Amaranthus tricolor, a C₄ vegetable amaranth of southeastern Asia. Maximum photosynthetic capacity was 48.3±1.0μmol CO₂ m^?2s^?1 and the temperature optimum was 35°C. The calculated intercellular CO₂ concentration at this leaf temperature and an incident photon flux (400–700 mm) of 2 mmol m^?2s^?1 averaged 208±14 μl l^?1, abnormally high for a C₄ species. The photosynthetic rate, intercellular CO₂ concentration, and leaf conductance all decreased with an increase in water vapor pressure deficit. However, the decrease in leaf conductance which resulted in a decrease in intercellular CO₂ concentration accounted for only one fourth of the observed decrease in photosynthetic rate as water vapor pressure deficit was increased. Subsequent measurements indicated that the depence of net photosynthesis on intercellular CO₂ concetration changed with water vapor pressure deficit.     

Biomass and leaf‐level gas exchange characteristics of three African savanna C4 grass species under optimum growth conditions

C₄ savanna grass species, Digitaria eriantha, Eragrostis lehmanniana and Panicum repens, were grown under optimum growth conditions with the aim of characterizing their above‐ and below‐ground biomass allocation and the response of their gas exchange to changes in light intensity, CO₂ concentration and leaf‐to‐air vapour pressure deficit gradient (D_l). Digitaria eriantha showed the largest above‐ and below‐ground biomass, high efficiency in carbon gain under light‐limiting conditions, high water use efficiency (WUE) and strong stomatal sensitivity to D_l (P = 0.002; r² = 0.5). Panicum repens had a high aboveground biomass and attained high light saturated photosynthetic rates (A_sat, 47 μmol m^?2 s^?1), stomatal conductance, (g_sat, 0.25 mol m^?2 s^?1) at relatively high WUE. Eragrostis lehmanniana had almost half the biomass of other species, and had similar A_sat and g_sat but were attained at lower WUE than the other species. This species also showed the weakest stomatal response to D_l (P = 0.19, r² = 0. 1). The potential ecological significance of the contrasting patterns of biomass allocation and variations in gas exchange parameters among the species are discussed.     

Arundo donax L. (Poaceae) — a C3 Species with Unusually High Photosynthetic Capacity

Gas exchange characteristics, chlorophyll a fluorescence and leaf water potential were investigated in the giant reed, Arundo donax, under natural conditions in an estuarine mangrove swamp in Durban, South Africa. Maximum photosynthetic CO₂ uptake ranged between 19.8 and 36.7 μmol m^?2 s^?1, depending on irradiance, and appeared to be regulated by leaf conductance. There was no saturation of CO₂ uptake or electron transport through PSII (ETR) with increasing irradiance up to 2500 μmol photons m^?2 s^?1. A linear relationship between CO₂ uptake, corrected for respiration (A), and ETR has only been reported for C₄ species and C₃ species when photorespiration is eliminated. From this relationship, it was calculated that 8.5 electrons were transported through PSII for the fixation of one mole of CO₂. Predawn leaf water potential was about ?0.5 MPa and decreased to ?1.5 MPa on a cloudy day and to ?2.1 MPa on a clear day. Diurnal change in leaf water potential had little influence on leaf conductance and hence CO₂ uptake. The molar water use efficiency (WUE) ranged between 4.1 and 9.3 μmol mmol^?1. Percentage photorespiration was between 36 and 39%.     

Interaction of ozone pollution and light effects on photosynthesis in a forest canopy experiment

Ozone pollution may reduce net carbon gain in forests, yet data from mature trees are rare and the effects of irradiance on the response of photosynthesis to ozone remain untested. We used an open-air system to expose 10 branches within the upper canopy of an 18-m-tall stand of sugar maple (Acer saccharum Marsh.) to twice-ambient concentrations of ozone (95nmol mol^?1, 0900 to 1700, 1 h mean) relative to 10 paired, untreated controls (45nmol mol^?1) over 3 months. The branch pairs were selected along a gradient from relatively high irradiance (PPFD 14.5 mol m^?2 d^?1) to deep shade (0.7mol m^?2 d^?1). Ozone reduced light-saturated rates of net photosynthesis (A_sat) and increased dark respiration by as much as 56 and 40%, respectively. Compared to sun leaves, shade leaves exhibited greater proportional reductions in A_sat and had lower chlorophyll concentrations, quantum efficiencies, and leaf absorptances when treated with ozone relative to controls. With increasing ozone dose over time, A_sat became uncoupled from stomatal conductance as ratios of internal to external concentrations of carbon dioxide increased, reducing water-use efficiency. Ozone reduced net photosynthesis and impaired stomatal function, with these effects depending on the irradiance environment of the canopy leaves. Increased ozone sensitivity of shade leaves compared to sun leaves has consequences for net carbon gain in canopies.     

Estimation of the anatomical, stomatal and biochemical components of differences in photosynthesis and transpiration of wild-type and transgenic (expressing yeast-derived invertase targeted to the vacuole) tobacco leaves

Photosynthesis and transpiration rates of transgenic (expressing yeast-derived invertase targeted to the vacuole) tobacco (Nicotiana tabacum L.) leaves were, respectively, 50 and 70% of those of a wild type at 20°C, 350 cm³ m^?3 CO₂ concentration, 450 μmol (photons) m^?2 s^?1 of light intensity, and 70% relative air humidity. These differences could be attributed: (a) to changes in leaf anatomy and, consequently, to changes in gases diffusion between the cells' surfaces and the atmosphere; (b) to different stomatal apertures, and, for the photosynthesis rate, (c) to the altered CO₂ assimilation rate. Our objective was to estimate the relative contributions of these three sources of difference. Measurements on the wild-type and the transgenic leaf cross-sections gave values for the cell area index (CAI, cell area surface per unit of leaf area surface) of 15.91 and 13.97, respectively. The two-dimensional model 2DLEAF for leaf gas exchange was used to estimate quantitatively anatomical, stomatal and biochemical components of these differences. Transpiration rate was equal to 0.9 for the wild-type and to 0.63 mmol m^?2 s^?1 for the transgenic leaf: 24.0% of the difference (0.066 mmol m^?2 s^?1 was caused by the greater cell area surface in the wild-type leaf, and 66.0% was caused by a smaller stomatal aperture in the transgenic leaf. Photosynthetic rate was 3.10 and 1.55 μmol m^?2 s^?1 for the wild-type and transgenic leaves, respectively. Only 10.3% of this difference (0.16 μmol m^?2 s^?1) was caused by the difference in CAI, and the remaining 89.7% was caused by altered CO₂ assimilation rate.     

Fluxes of carbon dioxide and water vapour over an undisturbed tropical forest in south-west Amazonia

• 1 Carbon dioxide and water vapour fluxes were measured for 55 days by eddy covariance over an undisturbed tropical rain forest in Rondonia, Brazil. Profiles of CO₂ inside the canopy were also measured.
• 2 During the night, CO₂ concentration frequently built up to 500 ppm throughout the canopy as a result of low rates of exchange with the atmosphere. In the early morning hours, ventilation of the canopy occurred.
• 3 Ecosystem gas exchange was calculated from a knowledge of fluxes above the canopy and changes of CO₂ stored inside the canopy. Typically, uptake by the canopy was 15 μmol m^?2 s^?1 in bright sunlight and dark respiration was 6-7 μmol m^?2 s^?1 The quantum requirement at low irradiance was: 40 mol photons per mol of CO₂.
• 4 Bulk stomatal conductance of the ecosystem was maximal in the early morning (0.4-1.0 mol m^?2 s^?1) and declined over the course of the day as leaf-to-air vapour pressure difference increased.

     

High-light effects on CO2 fixation gradients across leaves

Chlorophyll fluorescence and internal patterns of ¹⁴CO₂ fixation were measured in sun and shade leaves of spinach after treatment with various light intensities. When sun leaves were irradiated with 2000μmol m^?2 s^?1 for 2h, F_V/F_M decreased by about 15%, but ¹⁴CO₂ fixation was unaffected, whereas shade leaves exhibited a 21% decrease in F_v/F_M and a 25% decrease in ¹⁴CO₂ fixation. Irradiation of sun and shade leaves with 4000μmol m^?1 for 4 h decreased F_V/F_M by 30% in sun leaves and 40% in shade leaves, while total ¹⁴CO₂ fixation decreased by 41% in sun leaves and 55% in shade leaves. After light treatment, gradients of CO₂ fixation across leaves were determined by measuring ¹⁴CO₂ fixed in paradermal leaf sections after a 10s pulse of ¹⁴CO₂. Gradients of ¹⁴CO₂ fixation in control sun and shade leaves were identified when expressed on a relative basis and normalized for leaf depth. Treatment of leaves with 2000 μmol PAR m^?2 s^?1 for 2h did not after patterns of carbon fixation across sun leaves, but slightly altered the pattern in shade leaves. In contrast, treatment of sun and shade leaves with 4000μmol m^?2 s^?1 for 4h decreased carbon fixation more in the palisade mesophyll cells than in the spongy mesophyll cells of sun and shade leaves, and fixation in medial tissue of shade leaves was dramatically decreased compared to the adaxial and abaxial tissue. The interaction between leaf anatomy and biochemical parameters involved in tolerance to photoinhibition in spinach is discussed.     

Interactive effects of nitrogen and phosphorus on the acclimation potential of foliage photosynthetic properties of cork oak,Quercus suber,to elevated atmospheric CO2 concentrations

Leaf gas-exchange and chemical composition were investigated in seedlings of Quercus suber L. grown for 21 months either at elevated (700 μmol mol^–1) or normal (350 μmol mol^–1) ambient atmospheric CO₂ concentrations, [CO₂], in a sandy nutrient-poor soil with either ‘high’ N (0.3 mol N m^–3 in the irrigation solution) or with ‘low’ N (0.05 mol N m^–3) and with a constant suboptimal concentration of the other macro- and micronutrients. Although elevated [CO₂] yielded the greatest total plant biomass in ‘high’ nitrogen treatment, it resulted in lower leaf nutrient concentrations in all cases, independent of the nutrient addition regime, and in greater nonstructural carbohydrate concentrations. By contrast, nitrogen treatment did not affect foliar N concentrations, but resulted in lower phosphorus concentrations, suggesting that under lower N, P use-efficiency in foliar biomass production was lower. Phosphorus deficiency was evident in all treatments, as photosynthesis became CO₂ insensitive at intercellular CO₂ concentrations larger than ≈ 300 μmol mol^–1, and net assimilation rates measured at an ambient [CO₂] of 350 μmol mol^–1 or at 700 μmol mol^–1 were not significantly different. Moreover, there was a positive correlation of foliar P with maximum Rubisco (Ribulose-1,5-bisphosphate carboxylase/oxygenase) carboxylase activity (V_cmax), which potentially limits photosynthesis at low [CO₂], and the capacities of photosynthetic electron transport (J_max) and phosphate utilization (P_max), which are potentially limiting at high [CO₂]. None of these potential limits was correlated with foliar nitrogen concentration, indicating that photosynthetic N use-efficiency was directly dependent on foliar P availability. Though the tendencies were towards lower capacities of potential limitations of photosynthesis in high [CO₂] grown specimens, the effects were statistically insignificant, because of (i) large within-treatment variability related to foliar P, and (ii) small decreases in P/N ratio with increasing [CO₂], resulting in balanced changes in other foliar compounds potentially limiting carbon acquisition. The results of the current study indicate that under P-deficiency, the down-regulation of excess biochemical capacities proceeds in a similar manner in leaves grown under normal and elevated [CO₂], and also that foliar P/N ratios for optimum photosynthesis are likely to increase with increasing growth CO₂ concentrations. Symbols: A, net assimilation rate (μmol m^–2 s^–1); A_max, light-saturated A (μmol m^–2 s^–1); α, initial quantum yield at saturating [CO₂] and for an incident Q (mol mol^–1); [CO₂], atmospheric CO₂ concentration (μmol mol^–1); C_i, intercellular CO₂ concentration (μmol mol^–1); C_a, CO₂ concentration in the gas-exchange cuvette (μmol mol^–1); F_B, fraction of leaf N in ‘photoenergetics’; F_L, fraction of leaf N in light harvesting; F_R, fraction of leaf N in Rubisco; Γ*, CO₂ compensation concentration in the absence of R_d (μmol mol^–1); J_max*, capacity for photosynthetic electron transport; J_mc, capacity for photosynthetic electron transport per unit cytochrome f (mol e^–[mol cyt f]^–1 s^–1); K_c, Michaelis-Menten constant for carboxylation (μmol mol^–1); K_o, Michaelis-Menten constant for oxygenation (mmol mol^–1); M_A, leaf dry mass per area (g m^–2); O, intercellular oxygen concentration (mmol mol^–1); [P_i], concentration of inorganic phosphate (mM); P_max*, capacity for phosphate utilization; Q, photosynthetically active quantum flux density (μmol m^–2 s^–1); R_d*, day respiration (CO₂ evolution from nonphotorespiratory processes continuing in the light); Rubisco, ribulose-1,5-bisphosphate carboxylase/oxygenase; RUBP, ribulose-1,5-bisphosphate; T_l, leaf temperature (°C); U_TPU*, rate of triose phosphate utilization; V_cmax*, maximum Rubisco carboxylase activity; V_cr, specific activity of Rubisco (μmol CO₂[g Rubisco]^–1 s^–1] *given in either μmol m^–2 s^–1 or in μmol g^–1 s^–1 as described in the text.     

Seasonal trends of light-saturated net photosynthesis and stomatal conductance of loblolly pine trees grown in contrasting environments of nutrition, water and carbon dioxide

Repeated measures analysis was used to evaluate the effect of long-term CO₂ enhancement on seasonal trends of light-saturated rates of net photosynthesis (A_sat) and stomatal conductance to water vapour (g_sat) of 9-year-old loblolly pine (Pinus taeda L.) trees grown in a 2 × 2 factorial experimental design of nutrition and water. A significant interaction effect of CO₂ and nutrition on mean A_sat was observed for juvenile foliage. Also, juvenile foliage exposed to +350 μmol mol^?1 CO₂ had a higher rate of increase of A_sat between late summer and early autumn. This would lead to a greater potential for recharging carbohydrate reserves for winter. Mature foliage was affected by CO_sat, water and nutrient treatments in two ways. First, A_sat was significantly increased as a result of elevated CO₂ in January, a period when stomatal conductance was only 47% of the maximum observed rate. Secondly, the rate of increase of A_sat from winter to early spring was accelerated as a result of both nutrient + water and + 350 μmol mol^?1 CO₂ treatments. This accelerated response resulted in a greater potential for photosynthate production during the period when growth initiation occurred. Nutrient, water or carbon dioxide treatments did not significantly alter trends in g_sat for mature or juvenile foliage. A significant nutrition × CO₂ interaction was observed for the mature foliage, suggesting that g_sat increased with increasing CO₂ and nutrition. These results may have important consequences for the determination of the water use efficiency of loblolly pine. In spite of low g_sat in the winter to early spring period, there was a substantial gain in A_sat attributable to elevated CO₂ concentrations.     

Gas exchange,carbon balance and stomatal traits in wild and cultivated rice (<Emphasis Type="Italic">Oryza sativa</Emphasis> L.) genotypes

Carbon balancing within the plant species is an important feature for climatic adaptability. Photosynthesis and respiration traits are directly linked with carbon balance. These features were studied in 20 wild rice accessions Oryza spp., and cultivars. Wide variation was observed within the wild rice accessions for photosynthetic oxygen evolution or photosynthetic rate (A), dark (R _d), and light induced respiration (LIR) rates, as well as stomatal density and number. The mean rate of A varied from 10.49 μmol O₂ m^?2 s^?1 in cultivated species and 13.09 μmol O₂ m^?2 s^?1 in wild spp., The mean R _d is 2.09 μmol O₂ m^?2 s^?1 and 2.31 μmol O₂ m^?2 s^?1 in cultivated and wild spp., respectively. Light induced Respiration (LIR) was found to be almost twice in wild rice spp., (16.75 μmol O₂ m^?2 s^?1) compared to cultivated Oryza spp., Among the various parameters, this study reveals LIR and A as the key factors for positive carbon balance. Stomatal contribution towards carbon balance appears to be more dependent on abaxial surface where several number of stomata are situated. Correlation analysis indicates that R _d and LIR increase with the increase in A. In this study, O. nivara (CR 100100, CR 100097), O. rufipogon (IR 103404) and O. glumaepatula (IR104387) were identified as potential donors which could be used in rice breeding program. Co-ordination between gas exchange and patchiness in stomatal behaviour appears to be important for carbon balance and environmental adaptation of wild rice accessions, therefore, survival under harsh environment.     

Can light-saturated photosynthesis in lowland tropical forests be estimated by one light level?

Leaf-level net photosynthesis (A_n) estimates and associated photosynthetic parameters are crucial for accurately parameterizing photosynthesis models. For tropical forests, such data are poorly available and collected at variable light conditions. To avoid over- or underestimation of modeled photosynthesis, it is critical to know at which photosynthetic photon flux density (PPFD) photosynthesis becomes light-saturated. We studied the dependence of A_n on PPFD in two tropical forests in French Guiana. We estimated the light saturation range, including the lowest PPFD level at which A_sat (A_n at light saturation) is reached, as well as the PPFD range at which A_sat remained unaltered. The light saturation range was derived from photosynthetic light-response curves, and within-canopy and interspecific differences were studied. We observed wide light saturation ranges of A_n. Light saturation ranges differed among canopy heights, but a PPFD level of 1,000 µmol m⁻² s⁻¹ was common across all heights, except for pioneer trees species that did not reach light saturation below 2,000 µmol m⁻² s⁻¹. A light intensity of 1,000 µmol m⁻² s⁻¹ sufficed for measuring A_sat of climax species at our study sites, independent of the species or the canopy height. Because of the wide light saturation ranges, results from studies measuring A_sat at higher PPFD levels (for upper canopy leaves up to 1,600 µmol m⁻² s⁻¹) are comparable with studies measuring at 1,000 µmol m⁻² s⁻¹.     

The onset of photosynthetic acclimation to elevated CO2 partial pressure in field-grown Pinus radiata D. Don. after 4 years

The effects of CO₂ enrichment on photosynthesis and ribulose‐1,5‐bisphosphate carboxylase/oxygenase (rubisco) were studied in current year and 1‐year‐old needles of the same branch of field‐grown Pinus radiata D. Don trees. All measurements were made in the fourth year of growth in large, open‐top chambers continuously maintained at ambient (36 Pa) or elevated (65 Pa) CO₂ partial pressures. Photosynthetic rates of the 1‐year‐old needles made at the growth CO₂ partial pressure averaged 10·5 ± 0·5 μmol m^?2 s^?1 in the 36 Pa grown trees and 11·8 ± 0·4 μmol m^?2 s^?1 in the 65 Pa grown trees, and were not significantly different from each other. The photosynthetic capacity of 1‐year‐old needles was reduced by 25% from 23·0 ± 1·8 μmol m^?2 s^?1 in the 36 Pa CO₂ grown trees to 17·3 ± 0·7 μmol m^?2 s^?1 in the 65 Pa grown trees. Growth in elevated CO₂ also resulted in a 25% reduction in V_cmax (maximum carboxylation rate), a 23% reduction in J_max (RuBP regeneration capacity mediated by maximum electron transport rate) and a 30% reduction in Rubisco activity and content. Total non‐structural carbohydrates (TNC) as a fraction of total dry mass increased from 12·8 ± 0·4% in 1‐year‐old needles from the 36 Pa grown trees to 14·2 ± 0·7% in 1‐year‐old needles from the 65 Pa grown trees and leaf nitrogen content decreased from 1·30 ± 0·02 to 1·09 ± 0·10 g m^?2. The current‐year needles were not of sufficient size for gas exchange measurements, but none of the biochemical parameters measured (Rubisco, leaf chlorophyll, TNC and N), were effected by growth in elevated CO₂. These results demonstrate that photosynthetic acclimation, which was not found in the first 2 years of this experiment, can develop over time in field‐grown trees and may be regulated by source‐sink balance, sugar feedback mechanisms and nitrogen allocation.     

Seasonal variation in energy fluxes and carbon dioxide exchange for a broad-leaved semi-arid savanna (Mopane woodland) in Southern Africa

We studied the seasonal variation in carbon dioxide, water vapour and energy fluxes in a broad‐leafed semi‐arid savanna in Southern Africa using the eddy covariance technique. The open woodland studied consisted of an overstorey dominated by Colophospermum mopane with a sparse understorey of grasses and herbs. Measurements presented here cover a 19‐month period from the end of the rainy season in March 1999 to the end of the dry season September 2000. During the wet season, sensible and latent heat fluxes showed a linear dependence on incoming solar radiation (I) with a Bowen ratio (β) typically just below unity. Although β was typically around 1 at low incoming solar radiation (150 W m^?2) during the dry season, it increased dramatically with I, typically being as high as 4 or 5 around solar noon. Thus, under these water‐limited conditions, almost all available energy was dissipated as sensible, rather than latent heat. Marked spikes of CO₂ release occurred at the onset of the rainfall season after isolated rainfall events and respiration dominated the balance well into the rainfall season. During this time, the ecosystem was a constant source of CO₂ with an average flux of 3–5 μmol m^?2 s^?1 to the atmosphere during both day and night. But later in the wet season, for example, in March 2000 under optimal soil moisture conditions, with maximum leaf canopy development (leaf area index 0.9–1.3), the peak ecosystem CO₂ influx was as much as 10 μmol m^?2 s^?1. The net ecosystem maximum photosynthesis at this time was estimated at 14 μmol m^?2 s^?1, with the woodland ecosystem a significant sink for CO₂. During the dry season, just before leaf fall in August, maximum day‐ and night‐time net ecosystem fluxes were typically ?3 μmol m^?2 s^?1 and 1–2 μmol m^?2 s^?1, respectively, with the ecosystem still being a marginal sink. Over the course of 12 months (March 1999–March 2000), the woodland was more or less carbon neutral, with a net uptake estimated at only about 1 mol C m^?2 yr^?1. The annual net photosynthesis (gross primary production) was estimated at 32.2 mol m^?2 yr^?1.