Irradiance influences tea leaf (<Emphasis Type="Italic">Camellia sinensis</Emphasis> L.) photosynthesis and transpiration

Rates of net photosynthesis (P _N) and transpiration (E), and leaf temperature (T_L) of maintenance leaves of tea under plucking were affected by photosynthetic photon flux densities (PPFD) of 200–2 200 μmol m⁻² s⁻¹. P _N gradually increased with the increase of PPFD from 200 to 1 200 μmol m⁻² s⁻¹ and thereafter sharply declined. Maximum P _N was 13.95 μmol m⁻² s⁻¹ at 1 200 μmol m⁻² s⁻¹ PPFD. There was no significant variation of P _N among PPFD at 1 400–1 800 μmol m⁻² s⁻¹. Significant drop of P _N occurred at 2 000 μmol m⁻² s⁻¹. PPFD at 2 200 μmol m⁻² s⁻¹ reduced photosynthesis to 6.92 μmol m⁻² s⁻¹. PPFD had a strong correlation with T_L and E. Both T_L and E linearly increased from 200 to 2 200 μmol m⁻² s⁻¹ PPFD. T_L and E were highly correlated. The optimum T_L for maximum P _N was 26.0 °C after which P _N declined significantly. E had a positive correlation with P _N.     

Stomatal and non-stomatal limitations to photosynthesis in field-grown grapevine cultivars

Diurnal changes of photosynthesis in the leaves of grapevine (Vitis vinifera × V. labrusca) cultivars Campbell Early and Kyoho grown in the field were compared with respect to gas exchanges and actual quantum yield of photosystem 2 (Φ_PS2) in late May. Net photosynthetic rate (P_N) of the two cultivars rapidly increased in the morning, saturated at photosynthetic photon flux density (PPFD) from 1200 to 1500 μmol m⁻² s⁻¹ between 10:00 and 12:00 and slowly decreased after midday. Maximum P_N was 13.7 and 12.5 μmol m⁻² s⁻¹ in Campbell Early and Kyoho, respectively. The stomatal conductance (g_s) and transpiration rate changed in parallel with P_N, indicating that P_N was greatly affected by g_s. However, the decrease in P_N after midday under saturating PPFD was also associated with the observed depression of Φ_PS2 at high PPFD. The substantial increase in the leaf to air vapour pressure deficit after midday might also contribute to decline of g_s and P_N.     

Diurnal and seasonal trends in photosynthetic performance of <Emphasis Type="Italic">Dalbergia sissoo</Emphasis> Roxb. and <Emphasis Type="Italic">Hardwickia binata</Emphasis> Roxb. from a semi-arid ecosystem

Diurnal and seasonal trends in net photosynthetic rate (P _N), stomatal conductance (g), transpiration rate (E), vapour pressure deficit, temperature, photosynthetic photon flux density, and water use efficiency (WUE) were compared in a two-year-old Dalbergia sissoo and Hardwickia binata plantation. Mean daily maximum P _N in D. sissoo ranged from 21.40±2.60 μmol m⁻² s⁻¹ in rainy season I to 13.21±2.64 μmol m⁻² s⁻¹ in summer whereas in H. binata it was 20.04±1.20 μmol m⁻² s⁻¹ in summer and 13.64±0.16 μmol m⁻² s⁻¹ in winter. There was a linear relationship between daily maximum P _N and g _s in D. sissoo but there was no strong linear relationship between P _N and g _s in H. binata. In D. sissoo, the reduction in g _s led to a reduction in both P _N and E enabling the maintenance of WUE during dry season thereby managing unfavourable environmental conditions efficiently whereas in H. binata, an increase in g _s causes an increase of P _N and E with a significant moderate WUE.     

Changes of leaf water potential and gas exchange during and after drought in triticale and maize genotypes differing in drought tolerance

Influence of drought (D) on changes of leaf water potential (Ψ) and parameters of gas exchange in D-resistant and D-sensitive genotypes of triticale and maize was compared. Soil D (from −0.01 to −2.45 MPa) was simulated by mannitol solutions. At −0.013 MPa significant differences in Ψ, net photosynthetic rate (P _N), transpiration rate (E), stomatal conductance (g _s), and internal CO₂ concentration (C _i) of D-resistant and D-sensitive triticale and maize genotypes were not found. Together with the increase in concentration of the mannitol solution the impact of D on E and g _s for D-sensitive genotypes (CHD-12, Ankora) became lower than for the D-resistant ones (CHD-247, Tina). Inversely, impact of D on Ψ was higher in D-sensitive than D-resistant genotypes. From 1 to 3 d of D, a higher decrease in P _N was observed in D-resistant genotypes than in the D-sensitive ones. Under prolonged D (5–14 d) and simultaneous more severe D the decrease in P _N was lower in D-resistant than in D-sensitive genotypes. Changes in Ψ, P _N, E, and g _s caused by D in genotypes differing in the drought susceptibility were similar for triticale and maize. Compared to control plants, increase of C _i was different for triticale and maize genotypes. Hence one of the physiological reasons of different susceptibility to D between sensitive and resistant genotypes is more efficient protection of tissue water status in resistant genotypes reflected in higher decrease in g _s and limiting E compared to the sensitive ones. Other reason, observed in D-resistant genotypes during the recovery from D-stress, was more efficient removal of detrimental effects of D.     

Photosynthetic responses of apricot (<Emphasis Type="Italic">Prunus armeniaca</Emphasis> L.) to photosynthetic photon flux density,leaf temperature,and CO<Subscript>2</Subscript> concentration

Two cultivars (Katy and Erhuacao) of apricot (Prunus armeniaca L.) were evaluated under open-field and solar-heated greenhouse conditions in northwest China, to determine the effect of photosynthetic photon flux density (PPFD), leaf temperature, and CO₂ concentration on the net photosynthetic rate (P _N). In greenhouse, Katy registered 28.3 μmol m⁻² s⁻¹ for compensation irradiance and 823 μmol m⁻² s⁻¹ for saturation irradiance, which were 73 and 117 % of those required by Erhuacao, respectively. The optimum temperatures for cvs. Katy and Erhuacao were 25 and 35 °C in open-field and 22 and 30 °C in greenhouse, respectively. At optimal temperatures, P _N of the field-grown Katy was 16.5 μmol m⁻² s⁻¹, 21 % less than for a greenhouse-grown apricot. Both cultivars responded positively to CO₂ concentrations below the CO₂ saturation concentration, whereas Katy exhibited greater P _N (18 %) and higher carboxylation efficiency (91 %) than Erhuacao at optimal CO₂ concentration. Both cultivars exhibited greater photosynthesis in solar-heated greenhouses than in open-field, but Katy performed better than Erhuacao under greenhouse conditions.     

A coupled model of stomatal conductance and photosynthesis for winter wheat

The model couples stomatal conductance (g _s) and net photosynthetic rate (P _N) describing not only part of the curve up to and including saturation irradiance (I _max), but also the range above the saturation irradiance. Maximum stomatal conductance (g _smax) and I _max can be calculated by the coupled model. For winter wheat (Triticum aestivum) the fitted results showed that maximum P _N (P _max) at 600 μmol mol⁻¹ was more than at 350 μmol mol⁻¹ under the same leaf temperature, which can not be explained by the stomatal closure at high CO₂ concentration because g _smax at 600 μmol mol⁻¹ was less than at 350 μmol mol⁻¹. The irradiance-response curves for winter wheat had similar tendency, e.g. at 25 °C and 350 μmol mol⁻¹ both P _N and g _s almost synchronously reached the maximum values at about 1 600 μmol m⁻² s⁻¹. At 25 °C and 600 μmol mol⁻¹ the I _max corresponding to P _max and g _smax was 2 080 and 1 575 μmol m⁻² s⁻¹, respectively.     

Genotypic variation in photosynthesis in cacao is correlated with stomatal conductance and leaf nitrogen

Variation in photosynthetic parameters was observed between eight contrasting cacao (Theobroma cacao) genotypes. Net photosynthetic rate (P_N) ranged from 3.4 to 5.7 μmol(CO₂) m⁻² s⁻¹ for the genotypes IMC 47 and SCA 6, respectively. Furthermore, genotypic differences were detected in quantum efficiency ranging from 0.020 to 0.043 μmol(CO₂) μmol⁻¹(photon) for UF 676 and AMAZ 15/15, respectively. Differences in PN were correlated with both stomatal conductance (g_s) and leaf nitrogen per unit area. Some variation in water use efficiency was observed between genotypes, both intrinsic (P_N/g_s) and instantaneous (P_N/transpiration rate). Both measures of water use efficiency were a negative function of specific leaf area. Evidence was found for a trade-off mechanism between cacao genotypes in photosynthesis and leaf structure. High photosynthetic rate, expressed on a mass basis was associated with smaller leaves. Furthermore, thinner leaves were compensated for by a higher nitrogen content per unit mass.     

Compensatory effects of elevated CO<Subscript>2</Subscript> concentration on the inhibitory effects of high temperature and irradiance on photosynthetic gas exchange in carrots

We determined the interactive effects of irradiance, elevated CO₂ concentration (EC), and temperature in carrot (Daucus carota var. sativus). Plants of the cv. Red Core Chantenay (RCC) were grown in a controlled environmental plant growth room and exposed to 3 levels of photosynthetically active radiation (PAR) (400, 800, 1 200 μmol m⁻² s⁻¹), 3 leaf chamber temperatures (15, 20, 30 °C), and 2 external CO₂ concentrations (C _a), AC and EC (350 and 750 μmol mol⁻¹, respectively). Rates of net photosynthesis (P _N) and transpiration (E) and stomatal conductance (g _s ) were measured, along with water use efficiency (WUE) and ratio of internal and external CO₂ concentrations (C _i/C _a). P _N revealed an interactive effect between PAR and C _a. As PAR increased so did P _N under both C _a regimes. The g _s showed no interactive effects between the three parameters but had singular effects of temperature and PAR. E was strongly influenced by the combination of PAR and temperature. WUE was interactively affected by all three parameters. Maximum WUE occurred at 15 °C and 1 200 μmol m⁻² s^{− 1} PAR under EC. The C _i /C _a was influenced independently by temperature and C _a. Hence photosynthetic responses are interactively affected by changes in irradiance, external CO₂ concentration, and temperature. EC significantly compensates the inhibitory effects of high temperature and irradiance on P _N and WUE.     

Gas Exchange of Spring Barley and Wheat Grown under Mild Water Shortage

During mild water stress (decrease of full water capacity from 60 to 35 %) net photosynthetic rate (P _N) of four spring barley and wheat genotypes was about twice lower than that for unstressed plants and was mainly limited by non-stomatal factors. Availability of CO₂ from intercellular spaces did not change significantly when stomatal conductance (g _s) decreased from 0.25-0.35 to 0.15-0.20 mol(H₂O) m⁻² s⁻¹. There may be two main processes leading to similar intercellular CO₂ concentration (c _i) in stressed and unstressed seedlings despite of twice lower P _N under mild water stress: (a) lower diffusion of CO₂ through stomata represented by lower g _s, (b) lower consumption of CO₂ by photosynthetic apparatus of stressed plants. Last factor is partially pronounced by lower response of P _N to c _i observed for stressed than for control plants. This revised version was published online in August 2006 with corrections to the Cover Date.     

Differences in Field Gas Exchange and Water Relations Between a C3 Dicot (Plantago Asiatica) and a C4 Monocot (Eleusine Indica)

Field gas exchange and water potential in the leaves of a C₃ dicot, Plantago asiatica L., and a C₄ monocot, Eleusine indica Gaertn., which dominate in trampled vegetation in eastern Japan were surveyed during the growing periods for two consecutive years. Net photosynthetic rate (P _N) of E. indica increased with photosynthetic photon flux density (PPFD) and leaf temperature (T_L). P _N was not saturated at PPFDs above 1500 μmol m⁻² s⁻¹ and at T_L above 30 °C. On a sunny day in mid summer, maximum P _N was two times higher in E. indica than in P. asiatica [42 vs. 20 μmol(CO₂) m⁻² s⁻¹], but their transpiration rate (E) and the leaf water potential (Ψ_L) were similar. Soil-to-leaf hydraulic conductance, which probably plays a role in water absorption from the trampled compact soil, was higher in E. indica than in P. asiatica. The differences in photosynthetic traits between E. indica explain why E. indica communities more commonly develop at heavily trampled sites in summer than the P. asiatica communities. This revised version was published online in June 2006 with corrections to the Cover Date.     

Effects of different irradiances on the photosynthetic process during ex-vitro acclimation of Anoectochilus plantlets

Six months old in vitro-grown Anoectochilus formosanus plantlets were transferred to ex-vitro acclimation under low irradiance, LI [60 μmol(photon) m⁻² s⁻¹], intermediate irradiance, II [180 μmol(photon) m⁻² s⁻¹], and high irradiance, HI [300 μmol(photon) m⁻² s⁻¹] for 30 d. Imposition of II led to a significant increase of chlorophyll (Chl) b content, rates of net photosynthesis (P _N) and transpiration (E), stomatal conductance (g _s), electron transfer rate (ETR), quantum yield of electron transport from water through photosystem 2 (Φ_PS2), and activity of ribulose-1,5-bisphosphate carboxylase/ oxygenase (RuBPCO, EC 4.1.1.39). This indicates that Anoectochilus was better acclimated at II compared to LI treatment. On the other hand, HI acclimation led to a significant reduction of Chl a and b, P _N, E, g _s, photochemical quenching, dark-adapted quantum efficiency of open PS2 centres (F_v/F_m), probability of an absorbed photon reaching an open PS2 reaction centre (F_v′/F_m′), ETR, Φ_PS2, and energy efficiency of CO₂ fixation (Φ_CO2/Φ_PS2). This indicates that HI treatment considerably exceeded the photo-protective capacity and Anoectochilus suffered HI induced damage to the photosynthetic apparatus. Imposition of HI significantly increased the contents of antheraxanthin and zeaxanthin (ZEA), non-photochemical quenching, and conversion of violaxanthin to ZEA. Thus Anoectochilus modifies its system to dissipate excess excitation energy and to protect the photosynthetic machinery.     

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.     

Partitioning of photosynthetic electron flow between CO<Subscript>2</Subscript> assimilation and O<Subscript>2</Subscript> reduction in sunflower plants under water deficit

In sunflower (Helianthus annuus L.) grown under controlled conditions and subjected to drought by withholding watering, net photosynthetic rate (P _N) and stomatal conductance (g _s) of attached leaves decreased as leaf water potential (Ψ_w) declined from −0.3 to −2.9 MPa. Although g _s decreased over the whole range of Ψ_w, nearly constant values in the intercellular CO₂ concentrations (C _i) were observed as Ψ_w decreased to −1.8 MPa, but C _i increased as Ψ_w decreased further. Relative quantum yield, photochemical quenching, and the apparent quantum yield of photosynthesis decreased with water deficit, whereas non-photochemical quenching (q_NP) increased progressively. A highly significant negative relationship between q_NP and ATP content was observed. Water deficit did not alter the pyridine nucleotide concentration but decreased ATP content suggesting metabolic impairment. At a photon flux density of 550 μmol m⁻² s⁻¹, the allocation of electrons from photosystem (PS) 2 to O₂ reduction was increased by 51 %, while the allocation to CO₂ assimilation was diminished by 32 %, as Ψ_w declined from −0.3 to −2.9 MPa. A significant linear relationship between mean P _N and the rate of total linear electron transport was observed in well watered plants, the correlation becoming curvilinear when water deficit increased. The maximum quantum yield of PS2 was not affected by water deficit, whereas q_P declined only at very severe stress and the excess photon energy was dissipated by increasing q_NP indicating that a greater proportion of the energy was thermally dissipated. This accounted for the apparent down-regulation of PS2 and supported the protective role of q_NP against photoinhibition in sunflower.     

Relationship between allocation of absorbed light energy in PSII and photosynthetic rates of C3 and C4 plants

Two C₃ dicotyledonous crops and five C₄ monocotyledons treated with three levels of nitrogen were used to evaluate quantitatively the relationship between the allocation of absorbed light energy in PSII and photosynthetic rates (P _N) in a warm condition (25–26°C) at four to five levels [200, 400, 800, 1,200 (both C₃ and C₄) and 2,000 (C₄ only) μmol m⁻² s⁻¹] of photosynthetic photon flux density (PPFD). For plants of the same type (C₃ or C₄), there was a linear positive correlation between the fraction of absorbed light energy that was utilized in PSII photochemistry (P) and P _N, regardless of the broad range of their photosynthetic rates due to species-specific effect and/or nitrogen application; meanwhile, the fraction of absorbed light energy that was dissipated through non-photochemical quenching (D) showed a negative linear regression with P _N for each level of PPFD. The intercept of regression lines between P and P _N of C₃ and C₄ plants decreased, and that between D and P _N increased with increasing PPFD. With P and D as the main components of energy dissipation and complementary to each other, the fraction of excess absorbed light energy (E) was unchanged by P _N under the same level of PPFD. At the same level of P _N, C₄ plants had lower P and higher D than C₃ plants, due to the fact that C₄ plants with little or no photorespiration is considered a limited energy sink for electrons. Nevertheless there was a significant negative linear correlation between D and P when data from both C₃ and C₄ plants at varied PPFD levels was merged. The slope of regression lines between P and D was 0.85, indicating that in plants of both types, most of the unnecessary absorbed energy (ca. 85%) could dissipate through non-photochemical quenching, when P was inhibited by low P _N due to species-specific effect and nitrogen limitation at all levels of illumination used in the experiment.     

Intrinsic changes in photosynthetic parameters of carrot leaves under increasing CO<Subscript>2</Subscript> concentrations and soil moisture regimes

A controlled growth chamber experiment was conducted to investigate the short-term water use and photosynthetic responses of 30-d-old carrot seedlings to the combined effects of CO₂ concentration (50–1 050 μmol mol⁻¹) and moisture deficits (−5, −30, −55, and −70 kPa). The photosynthetic response data was fitted to a non-rectangular hyperbola model. The estimated parameters were compared for effects of moisture deficit and elevated CO₂ concentration (EC). The carboxylation efficiency (α) increased in response to mild moisture stress (−30 kPa) under EC when compared to the unstressed control. However, moderate (−55 kPa) and extreme (−70 kPa) moisture deficits reduced α under EC. Maximum net photosynthetic rate (P _Nmax) did not differ between mild water deficit and unstressed controls under EC. Moderate and extreme moisture deficits reduced P _Nmax by nearly 85 % compared to controls. Dark respiration rate (R _D) showed no consistent response to moisture deficit. The CO₂ compensation concentration (Γ) was 324 μmol mol⁻¹ for −75 kPa and ranged 63–93 μmol mol⁻¹ for other moisture regimes. Interaction between moisture deficit and EC was noticed for P _N, ratio of intercellular and ambient CO₂ concentration (C _i/C _a), stomatal conductance (g _s ), and transpiration rate (E). P _N was maximum and C _i/C _a was minimum at −30 kPa moisture deficit and at C _a of 350 μmol mol⁻¹. The g _s and E showed an inverse relationship at all moisture deficit regimes and EC. Water use efficiency (WUE) increased with moisture deficit up to −55 kPa and declined thereafter. EC showed a positive influence towards sustaining P _N and increasing WUE only under mild moisture stress, and no beneficial effects of EC were noticed at moderate or extreme moisture deficits.     

Effect of high temperature on photosynthesis and transpiration of sweet corn (<Emphasis Type="Italic">Zea mays</Emphasis> L. var. <Emphasis Type="Italic">rugosa</Emphasis>)

Four temperature treatments were studied in the climate controlled growth chambers of the Georgia Envirotron: 25/20, 30/25, 35/30, and 40/35 °C during 14/10 h light/dark cycle. For the first growth stage (V3-5), the highest net photosynthetic rate (P _N) of sweet corn was found for the lowest temperature of 28–34 μmol m⁻² s⁻¹ while the P _N for the highest temperature treatment was 50–60 % lower. We detected a gradual decline of about 1 P _N unit per 1 °C increase in temperature. Maximum transpiration rate (E) fluctuated between 0.36 and 0.54 mm h⁻¹ (≈5.0–6.5 mm d⁻¹) for the high temperature treatment and the minimum E fluctuated between 0.25 and 0.36 mm h⁻¹ (≈3.5–5.0 mm d⁻¹) for the low temperature treatment. Cumulative CO₂ fixation of the 40/35 °C treatment was 33.7 g m⁻² d⁻¹ and it increased by about 50 % as temperature declined. The corresponding water use efficiency (WUE) decreased from 14 to 5 g(CO₂) kg⁻¹(H₂O) for the lowest and highest temperature treatments, respectively. Three main factors affected WUE, P _N, and E of Zea: the high temperature which reduced P _N, vapor pressure deficit (VPD) that was directly related to E but did not affect P _N, and quasi stem conductance (QC) that was directly related to P _N but did not affect E. As a result, WUE of the 25/20 °C temperature treatment was almost three times larger than that of 40/35 °C temperature treatment.     

Variable responses of mesophyll conductance to substomatal carbon dioxide concentration in common bean and soybean

Some reports indicate that mesophyll conductance (g _m) to carbon dioxide varies greatly with the substomatal carbon dioxide concentration (C _i) during the measurement, while other reports indicate little or no change in g _m with C _i. I used the oxygen sensitivity of photosynthesis to determine the response of g _m to C _i over the range of about 100 to 300 μmol mol⁻¹ C _i at constant temperature in common bean (Phaseolus vulgaris) and soybean (Glycine max) grown over a range of temperatures and photosynthetic photon flux densities (PPFD). In soybean grown and measured at high PPFD there was only a slight, approximately 15% decrease in g _m with C _i over the range of 100 to 300 μmol mol⁻¹. With lower PPFD during the measurement of g _m, and especially with low PPFD during plant growth, there was a larger decrease in g _m with C _i in soybean. In common bean, the same range in C _i resulted in about a 60% decrease in g _m for plants grown and measured at high PPFD, with an even larger decrease for plants at low growth or measurement PPFD. Growth temperatures of 20 to 30°C had little influence on the response of g _m to C _i or its absolute value in either species. It is concluded that these two species differed substantially in the sensitivity of g _m to C _i, and that PPFD but not temperature during leaf development strongly affected the response of g _m to C _i.     

Carbon Dioxide Assimilation,Transpiration, and Leaf Conductance of Bean (Phaseolus Vulgaris L.) Under Blue and Red Radiation

In bean (Phaseolus vulgaris L.) seedlings well supplied with water, rates of transpiration (E) and CO₂ assimilation (P _N) of the primary leaves were measured under blue (BR) or red (RR) irradiance of 150 µmol(photon) m^–2 s^–1. The leaf conductance to H₂O vapour transfer (g _H2O), as well as the intercellular concentrations of H₂O vapour (e _i) and of CO₂ (C _i) were calculated. Under BR, g _H2O was significantly greater, but P _N was lower, and E similar as compared with corresponding values found under RR. The increase of stomata aperture under BR was evident although C _i was higher and e _i was lower than under RR. Results agree with the suggestion that BR directly activates guard cell metabolism and in well watered plants determines mainly the stomata aperture.     

Photosynthetic characteristics of dipterocarp species planted on degraded sandy soils in southern Thailand

To elucidate whether dipterocarp species, dominant late-successional species of tropical forests in Southeast Asia, actually have a disadvantage when planted on open site in terms of their photosynthetic characteristics, we investigated photosynthesis in dipterocarp seedlings planted in the open on degraded sandy soils in southern Thailand. These species were compared with seedlings of Acacia mangium Willd., a fast-growing tropical leguminous tree, which is often planted on degraded open site in Southeast Asia. The dipterocarp seedlings had an irradiance-saturated net photosynthetic rate (P _N), stomatal conductance (g _s), carboxylation efficiency, and photosynthetic capacity comparable to or superior to those of A. mangium. In particular, seedlings of Dipterocarpus obtusifolius Teijsm. ex Miq. showed an irradian-ce-saturated P _N of 21 μmol m⁻² s⁻¹, a value higher than any previously reported for a dipterocarp species, accompanied by high g _s (0.7 mol m⁻² s⁻¹) and high photosynthetic capacity. Thus dipterocarp species do not necessarily have a disadvantage in terms of their photosynthetic characteristics on open sites with degraded sandy soils.     

What is the usual internal carbon dioxide concentration in C<Subscript>4</Subscript> species under midday field conditions?

The carbon dioxide concentrating system in C₄ photosynthesis allows high net photosynthetic rates (P _N) at low internal carbon dioxide concentrations (C _i), permitting higher P _N relative to stomatal conductance (g _s) than in C₃ plants. This relation would be reflected in the ratio of C _i to external ambient (C _a) carbon dioxide concentration, which is often given as 0.3 or 0.4 for C₄ plants. For a C _a of 360 μmol mol⁻¹ that would mean a C _i about 110–140 μmol mol⁻¹. Our field observations made near midday on three weedy C₄ species, Amaranthus retroflexus, Echinochloa crus-galli, and Setaria faberi, and the C₄ crop Sorghum bicolor indicated mean values of C _i of 183–212 μ mol mol⁻¹ at C _a = 360 μmol mol⁻¹. Measurements in two other C₄ crop species grown with three levels of N fertilizer indicated that while midday values of C _i at high photon flux were higher at limiting N, even at high nitrogen C _i averaged 212 and 196 μmol mol⁻¹ for Amaranthus hypochondriacus and Zea mays, respectively. In these two crops midday C _i decreased with increasing leaf to air water vapor pressure difference. Averaged over all measurement days, the mean C _i across all C₄ species was 198 μmol mol⁻¹, for a C _i/C _a ratio of 0.55. Prior measurements on four herbaceous C₃ species using the same instrument indicated an average C _i/C _a ratio of 0.69. Hence midday C _i values in C ₄ species under field conditions may often be considerably higher and more similar to those of C₃ species than expected from measurements made on plants in controlled environments. Reducing g _s in C₄ crops at low water vapor pressure differences could potentially improve their water use efficiency without decreasing P _N.