Water-water cycle involved in dissipation of excess photon energy in phosphorus deficient rice leaves

The water-water cycle which may be helpful for dissipating the excitation pressure over electron transport chain and minimizing the risk of photoinhibition and photodamage was investigated in rice after 10-d P-deficient treatment. Net photosynthetic rate decreased under P-deficiency, thus the absorption of photon energy exceeded the energy required for CO₂ assimilation. A more sensitive response of effective quantum yield of photosystem 2 (Φ_PS2) to O₂ concentration was observed in plants that suffered P starvation, indicating that more electrons were transported to O₂ in the P-deficient leaves. The electron transport rate through photosystem 2 (PS 2) (J_f) was stable, and the fraction of electron transport rate required to sustain CO₂ assimilation and photorespiration (J_g/J_f) was significantly decreased accompanied by an increase in the alternative electron transport (J_a/J_f), indicating that a considerable electron amount had been transported to O₂ during the water-water cycle in the P-deficient leaves. However, the fraction of electron transport to photorespiration (J_o/J_f) was also increased in the P-deficient leaves and it was less sensitive than that of water-water cycle. Therefore, water-water cycle could serve as an efficient electron sink. The higher non-photochemical fluorescence quenching (q_N) in the P-deficient leaves depended on O₂ concentration, suggesting that the water-water cycle might also contribute to non-radiative energy dissipation. Hence, the enhanced activity of the water-water cycle is important for protecting photosynthetic apparatus under P-deficiency in rice.     

A role for brassinosteroids in the regulation of photosynthesis in Cucumis sativus

The effects of 24-epibrassinolide (EBR) spray application on gas-exchange, chlorophyll fluorescence characteristics, Rubisco activity, and carbohydrate metabolism were investigated in cucumber (Cucumis sativus L. cv. Jinchun No. 3) plants grown in a greenhouse. EBR significantly increased the light-saturated net CO(2) assimilation rate (A(sat)) from 3 h to 7d after spraying, with 0.1 mg l(-1) EBR proving most effective. Increased A(sat) in EBR-treated leaves was accompanied by increases in the maximum carboxylation rate of Rubisco (V(c,max)) and in the maximum rate of RuBP regeneration (J(max)). EBR-treated leaves also had a higher quantum yield of PSII electron transport (phi(PSII)) than the controls, which was mainly due to a significant increase in the photochemical quenching (q(P)), with no change in the efficiency of energy capture by open PSII reaction centres (F'(v)/F'(m)). EBR did not influence photorespiration. In addition, significant increases in the initial activity of Rubisco and in the sucrose, soluble sugars, and starch contents were observed followed by substantial increases in sucrose phosphate synthase (SPS), sucrose synthase (SS), and acid invertase (AI) activities after EBR treatment. It was concluded that EBR increases the capacity of CO(2) assimilation in the Calvin cycle, which was mainly attributed to an increase in the initial activity of Rubisco.     

青藏高原药用植物唐古特山莨菪和唐古特大黄光合作用对强光的响应

与唐古特大黄相比,唐古特山莨菪的表观光合量子效率(AQY)较高,但最大净光合速率(Pmax)较低。在光强小于1200μmolm-2s-1时,后者用于碳同化的电子传递占总光合电子传递的比例(JC/JF)比前者高,而分配于光呼吸的电子传递(JO/JF)及Rubisco氧化和羧化速率的比值(VO/VC)则相反;光强大于1200μmolm-2s-1以后两种植物的这些参数都趋向稳定。随光强增加,后者叶片吸收光能分配于热耗散(D)的增加斜率较前者高,表明两高山植物对强辐射的适应方式略有不同。加强光呼吸途径的耗能代谢和PSII天线热耗散份额是唐古特山莨菪适应高原强辐射的主要方式,而提高叶片光合能力则是唐古特大黄的一种适应方式。     

The lack of mitochondrial complex I in a CMSII mutant of Nicotiana sylvestris increases photorespiration through an increased internal resistance to CO2 diffusion

The cytoplasmic male sterile II (CMSII) mutant lacking complex I of the mitochondrial electron transport chain has a lower photosynthetic activity but exhibits higher rates of excess electron transport than the wild type (WT) when grown at high light intensity. In order to examine the cause of the lower photosynthetic activity and to determine whether excess electrons are consumed by photorespiration, light, and intercellular CO(2), molar fraction (c(i)) response curves of carbon assimilation were measured at varying oxygen molar fractions. While oxygen is the major acceptor for excess electrons in CMSII and WT leaves, electron flux to photorespiration is favoured in the mutant as compared with the WT leaves. Isotopic mass spectrometry measurements showed that leaf internal conductance to CO(2) diffusion (g(m)) in mutant leaves was half that of WT leaves, thus decreasing the c(c) and favouring photorespiration in the mutant. The specificity factor of Rubisco did not differ significantly between both types of leaves. Furthermore, carbon assimilation as a function of electrons used for carboxylation processes/electrons used for oxygenation processes (J(C)/J(O)) and as a function of the calculated chloroplastic CO(2) molar fraction (c(c)) values was similar in WT and mutant leaves. Enhanced rates of photorespiration also explain the consumption of excess electrons in CMSII plants and agreed with potential ATP consumption. Furthermore, the lower initial Rubisco activity in CMSII as compared with WT leaves resulted from the lower c(c) in ambient air, since initial Rubisco activity on the basis of equal c(c) values was similar in WT and mutant leaves. The retarded growth and the lower photosynthetic activity of the mutant were largely overcome when plants were grown in high CO(2) concentrations, showing that limiting CO(2) supply for photosynthesis was a major cause of the lower growth rate and photosynthetic activity in CMSII.     

施氮和大气CO2浓度升高对小麦旗叶光合电子传递和分配的影响

采用开顶式气室盆栽培养小麦,设计2个大气CO2浓度(正常:400 μmol.mol-1;高:760 μmol·mol-1)、2个氮素水平(0和200 mg·kg-1土)的组合处理,通过测定小麦抽穗期旗叶氮素和叶绿素浓度、光合速率(Pn)-胞间CO2浓度(C1)响应曲线及荧光动力学参数,来测算小麦叶片光合电子传递速率等,研究了高大气CO2浓度下施氮对小麦旗叶光合能量分配的影响.结果表明:与正常大气CO2浓度相比,高大气CO2浓度下小麦叶片氮浓度和叶绿素浓度降低,高氮处理的小麦叶片叶绿素a/b升高.施氮后小麦叶片PSⅡ最大光化学效率(Fv/Fm)、PSⅡ反应中心最大量子产额(Fv'/Fm')、PSⅡ反应中心的开放比例(qr)和PSⅡ反应中心实际光化学效率(φPSⅡ)在大气CO2浓度升高后无明显变化,虽然叶片非光化学猝灭系数(NPQ)显著降低,但PSⅡ总电子传递速率(JF)无明显增加;不施氮处理的Fv'/Fm'、φPSⅡ和NPQ在高大气CO2浓度下显著降低,尽管Fv/Fm和qp无明显变化,JF仍显著下降.施氮后小麦叶片JF增加,参与光化学反应的非环式电子流传递速率(Jc)明显升高.大气CO2浓度升高使参与光呼吸的非环式电子流传递速率(J0)、Rubisco氧化速率(V0)、光合电子的光呼吸/光化学传递速率比(J0/Jc)和Rubisco氧化/羧化比(V0/Vc)降低,但使Jc和Rubisco羧化速率(Vc)增加.因此,高大气CO2浓度下小麦叶片氮浓度和叶绿素浓度降低,而增施氮素使通过PSⅡ反应中心的电子流速率显著增加,促进了光合电子流向光化学方向的传递,使更多的电子进入Rubisco羧化过程,Pn显著升高.     

Processes contributing to photoprotection of grapevine leaves illuminated at low temperature

Photoinactivation of photosystem II (PSII) and energy dissipation at low leaf temperatures were investigated in leaves of glasshouse-grown grapevine ( Vitis vinifera L. cv. Riesling). At low temperatures (< 15°C), photosynthetic rates of CO₂ assimilation were reduced. However, despite a significant increase in the amount of light excessive to that required by photosynthesis, grapevine leaves maintained high intrinsic quantum efficiencies of PSII ( F _v/ F _m) and were highly resistant to photoinactivation compared to other species. Non-photochemical energy dissipation involving xanthophylls and fast D1 repair were the main protective processes reducing the 'gross' rate of photoinactivation and the 'net' rate of photoinactivation, respectively. We developed an improved method of energy dissipation analysis that revealed up to 75% of absorbed light is dissipated thermally via pH- and xanthophyll-mediated non-photochemical quenching at low temperatures (5–15°C) and moderate (800 µmol quanta m⁻² s⁻¹) light. Up to 20% of the energy flux contributing to electron transport was dissipated via photorespiration when taking into account temperature-dependent mesophyll conductance; however, this flux used in photorespiration was only a relatively small amount of the total absorbed light energy. Photoreduction of O₂ at photosystem I (PSI) and subsequent superoxide detoxification (water-water cycle) was more sensitive to inhibition by low temperature than photorespiration. Therefore the water-water cycle represents a negligibly small energy sink below 15°C, irrespective of mesophyll conductance.     

The water-water cycle in leaves is not a major alternative electron sink for dissipation of excess excitation energy when CO(2) assimilation is restricted

Electron flux from water via photosystem II (PSII) and PSI to oxygen (water-water cycle) may provide a mechanism for dissipation of excess excitation energy in leaves when CO(2) assimilation is restricted. Mass spectrometry was used to measure O(2) uptake and evolution together with CO(2) uptake in leaves of French bean and maize at CO(2) concentrations saturating for photosynthesis and the CO(2) compensation point. In French bean at high CO(2) and low O(2) concentrations no significant water-water cycle activity was observed. At the CO(2) compensation point and 3% O(2) a low rate of water-water cycle activity was observed, which accounted for 30% of the linear electron flux from water. In maize leaves negligible water-water cycle activity was detected at the compensation point. During induction of photosynthesis in maize linear electron flux was considerably greater than CO(2) assimilation, but no significant water-water cycle activity was detected. Miscanthus × giganteus grown at chilling temperature also exhibited rates of linear electron transport considerably in excess of CO(2) assimilation; however, no significant water-water cycle activity was detected. Clearly the water-water cycle can operate in leaves under some conditions, but it does not act as a major sink for excess excitation energy when CO(2) assimilation is restricted.     

In memory of Thomas Turpin Bannister (1930–2018)

Plants grown in the field experience sharp changes in irradiation due to shading effects caused by clouds, other leaves, etc. The excess of absorbed light energy is dissipated by a number of mechanisms including cyclic electron transport, photorespiration, and Mehler-type reactions. This protection is essential for survival but decreases photosynthetic efficiency. All phototrophs except angiosperms harbor flavodiiron proteins (Flvs) which relieve the excess of excitation energy on the photosynthetic electron transport chain by reducing oxygen directly to water. Introduction of cyanobacterial Flv1/Flv3 in tobacco chloroplasts resulted in transgenic plants that showed similar photosynthetic performance under steady-state illumination, but displayed faster recovery of various photosynthetic parameters, including electron transport and non-photochemical quenching during dark–light transitions. They also kept the electron transport chain in a more oxidized state and enhanced the proton motive force of dark-adapted leaves. The results indicate that, by acting as electron sinks during light transitions, Flvs contribute to increase photosynthesis protection and efficiency under changing environmental conditions as those found by plants in the field.     

End product feedback effects on photosynthetic electron transport

The inhibition of photosynthetic electron transport when starch and sucrose synthesis limit the overall rate of photosynthesis was studied inPhaseolus vulgaris L. andXanthium strumarium L. The starch and sucrose limitation was established by reducing photorespiration by manipulation of the partial pressure of O₂ and CO₂. Chlorophylla fluorescence quenching, the redox state of Photosystem I (estimated by the redox status of NADP-dependent malate dehydrogenase), and the intermediates of the xanthophyll cycle were investigated. Non-photochemical fluorescence quenching increased, NADP-dependent malate dehydrogenase remained at 100% activity, and the amount of violaxanthin decreased when starch and sucrose synthesis limited photosynthesis. In addition, O₂-induced feedback caused a decrease in photochemical quenching. These results are consistent with a downward regulation of photosynthetic electron transport during end product feedback on photosynthesis. When leaves were held in high CO₂ for 4 hours, the efficiency of Photosystem II was reduced when subsequently measured under low light. The results indicate that the quantum efficiency of open Photosystem II centers was reduced by the 4 hour treatment. We interpret the results to indicate that feedback from starch and sucrose synthesis on photosynthetic electron transport stimulates mechanisms for dissipating excess light energy but that these mechanisms do not completely protect leaves from long-term inhibition of photosynthetic electron transport capacity.     

Non-photochemical loss in PSII in high- and low-light-grown leaves of Vicia faba quantified by several fluorescence parameters including L(NP), F0/F'm, a novel parameter

Using the expression of fluorescence originated from the PSII open reaction center in the light by Oxborough and Baker (1997), we obtained a formula that expresses relationships between the quantum efficiency of PSII photochemistry in the dark (Phi(m)= F(v)/F(m)) and in the light Phi'(m)=F'(v)/F'(m):Phi'(m)=Phi(m)+L(NP), where L(NP)(=F(0)/F'(m)) denotes the quantum yield of light induced non-photochemical losses (heat dissipation and fluorescence de-excitation) in PSII. Using L(NP) and other conventional fluorescence parameters, we conducted quenching analyses with leaves of broad bean plants (Vicia faba L.) grown at 700 (high light; HL) and 80 mumol photons m(-2) s(-1) (low light; LL). We also examined whether behavior of q(0) quenching (q(0)=1-F'(0)/F(0)) is related to the reaction center quenching. When the actinic light (AL) was strong, Stern-Volmer quenching [NPQ=(F(m)-F'(m))/F'(m)] and L(NP) increased rapidly and then decreased slowly in HL leaves, while, in LL leaves, they increased slowly. It is probable that rapid formation of a large proton gradient was responsible for sharp rises in both parameters in HL leaves. The steady-state 'excess' parameter [Phi(Ex)= (1 - qP) Phi(m)/(Phi(m)+ L(NP))], fraction of energy migrating to closed PSII centers, increased with the photon flux density of AL in LL leaves. In contrast, in HL leaves, Phi(Ex) did not increase markedly. The examination of the relationship between Phi(Ex) and L(NP) obtained at various AL revealed that in LL leaves the increase in (1 - qP) with the increase in AL prevailed, while, in HL leaves, the increase in L(NP) suppressed the increase in (1 - qP). Using the difference between L(NP) and L(D) (Phi(ND)= L(NP)- L(D), where L(D)= F(0)/F(m)), q(0) and qN (=1-F'(v)/F(v)) were calculated without using measured F'(0). The relationships between q(0) and qN thus obtained for various AL levels were almost identical for both HL and LL leaves, implying no difference in the fluorescence origin between the HL and LL leaves. Usefulness of these equations expressing non-photochemical loss is discussed.     

田间条件下海岛棉和陆地棉花铃期叶片光保护的机制

研究海岛棉(Gossypium barbadense)和陆地棉(G. hirsutum)两个棉花栽培种的光合作用特性, 探讨两个栽培种光合机构的光抑制以及防御保护机制, 以期为新疆棉花高光效品种选育和高产高效栽培实践提供理论基础。在新疆生态气候条件下, 系统测定了海岛棉和陆地棉的叶片运动、叶片接受光量子通量密度(PFD)、叶片温度、叶绿素荧光参数、气体交换参数和光呼吸速率的日变化。研究结果表明: 陆地棉叶片的“横向日性”较强而海岛棉较弱, 导致海岛棉叶片接受PFD较低, 但其叶片温度较高。海岛棉叶片的光合速率和气孔导度均显著低于陆地棉。在8:00-10:00 (北京时间, 下同)海岛棉叶片的光呼吸速率略低于陆地棉, 其余时间段海岛棉和陆地棉叶片的光呼吸速率相似。不同栽培种间, 叶片的最大光化学效率和实际光化学效率的日变化均无明显差异。除14:00-16:00以外, 海岛棉叶片的表观电子传递速率和光化学猝灭系数均显著低于陆地棉。8:00以后, 海岛棉叶片的非光化学猝灭显著高于陆地棉。因此, 在新疆生态气候条件下, 海岛棉和陆地棉叶片“横向日性”运动能力和气孔导度的差异导致叶片所处的光温环境不同, 同时造成海岛棉叶片的碳同化能力较低。为阻止光合电子传递链的过度还原, 减轻光合机构的光抑制, 陆地棉叶片主要通过光合机构的电子流途径耗散激发能, 而海岛棉叶片通过热耗散途径和相对较高的光呼吸能力来耗散激发能。     

不同施氮量对杂交酸模叶片光合电子流分配的影响

研究了不同施氮量对高蛋白含量植物杂交酸模(Rumex patientiaxR.tianschanicus)叶片中总光合电子流和分配在碳同化、光呼吸、Mehler反应以及氮代谢上的光合电子流的影响,并研究了不同施氮量对硝酸还原酶(NR)和谷氨酰胺合成酶(GS)的活性、叶片的蛋白质含量及叶绿素含量的影响。结果表明随着施氮量的增加,硝酸还原酶和谷氨酰胺合成酶的活性都显著提高,同时更多的光合电子流分配到氮代谢和光呼吸。氮代谢所需光合电子流约占总光合电子流的15%～21%。缺氮并没有造成光合电子流向Mehler反应分配的增加。     

Influence of Potassium Deficiency on Photosynthesis,Chlorophyll Content,and Chloroplast Ultrastructure of Cotton Plants

In cotton (Gossypium hirsutum L.) grown in controlled-environment growth chamber the effects of K deficiency during floral bud development on leaf photosynthesis, contents of chlorophyll (Chl) and nonstructural saccharides, leaf anatomy, chloroplast ultrastructure, and plant dry matter accumulation were studied. After cotton plants received 35-d K-free nutrient solution at the early square stage, net photosynthetic rate (P _N) of the uppermost fully expanded main-stem leaves was only 23 % of the control plants receiving a full K supply. Decreased leaf P _N of K-deficient cotton was mainly associated with dramatically low Chl content, poor chloroplast ultrastructure, and restricted saccharide translocation, rather than limited stomata conductance in K-deficient leaves. Accumulation of sucrose in leaves of K-deficient plants might be associated with reduced entry of sucrose into the transport pool or decreased phloem loading. K deficiency during squaring also dramatically reduced leaf area and dry matter accumulation, and affected assimilate partitioning among plant tissues.     

Oxygen reduction in the Mehler reaction is insufficient to protect photosystems I and II of leaves against photoinactivation

The relative roles of assimilatory and photorespiratory electron flows on one side and of the Mehler‐peroxidase pathway on the other side in sustaining electron transport and providing protection against photoinhibition were investigated in leaves of spinach ( Spinacia oleracea L.) and sunflower ( Helianthus annuus L.). After inhibiting photosynthesis and photorespiration of intact leaves by either HCN or glycolaldehyde, light‐dependent linear electron transport was decreased by more than 90% at a photon flux density of 800 µmol m⁻² s⁻¹. Remaining electron transport exhibited characteristics of the Mehler reaction. Nonphotochemical quenching of chlorophyll fluorescence increased after inhibition of CO₂ assimilation and photorespiration indicating effective dissipation of excess excitation energy. Nevertheless, appreciable photoinactivation was observed under these conditions not only of photosystem II but also of photosystem I. This damage was oxygen‐dependent. It was much reduced or absent when the oxygen concentration of the atmosphere was reduced from 21 to 1%.     

Photorespiration is Essential for the Protection of the Photosynthetic Apparatus of C3 Plants Against Photoinactivation Under Sunlight

CO₂ assimilation, transpiration and modulated chlorophyll fluorescence of leaves of Chenopodium bonus-henricus (L.) were measured in the laboratory and, at a high altitude location, in the field. Direct calibration of chlorophyll fluorescence parameters against carbon assimilation in the presence of 1 or 0.5% oxygen (plus CO₂) proved necessary to calculate electron transport under photorespiratory conditions in individual experiments. Even when stomata were open in the field, total electron transport was two to three times higher in sunlight than indicated by net carbon gain. It decreased when stomata were blocked by submerging leaves under water or by forcing them to close in air by cutting the petiole. Even under these conditions, electron transport behind closed stomata approached 10 nmol electrons m^?2 leaf area s^?1 at temperatures between 25 and 30 °C. No photoinactivation of photosystem II was indicated by fluorescence analysis after a day's exposure to full sunlight. Only when leaves were submerged in ice was appreciable photoinactivation noticeable after 4 h exposure to sunlight. Even then almost full recovery occurred overnight. Electron transport behind blocked stomata was much decreased when leaves were darkened for 70 min (in order to deactivate light-regulated enzymes of the Calvin cycle) before exposure to full sunlight. Brief exposure of leaves to HCN (to inhibit photoassimilation and photorespiration) also decreased electron transport drastically compared to electron transport in unpoisoned leaves with blocked stomata. Non-photochemical fluorescence quenching and reduction of Q_A, the primary electron acceptor of photosystem II was increased by HCN-poisoning. Very similar observations were made when glyceraldehyde was used instead of HCN to inhibit photosynthesis and photorespiration. In HCN-poisoned leaves, residual electron transport increased linearly with temperature and showed early light saturation revealing characteristics of the Mehler reaction. During short exposure of these leaves to photon flux densities equivalent to 25% of sunlight, no or only little photoinactivation of photosystem II was observed. However, prolonged exposure to sunlight caused inactivation even though non-photochemical quenching of chlorophyll fluorescence was extensive. Simultaneously, oxidation of cellular ascorbate and glutathione increased. Inactivation of photosystem II was reversible in dim light and in the dark only after short times of exposure to sunlight. Glyceraldehyde was very similar to HCN in increasing the sensitivity of photosystem II in leaves to sunlight. We conclude from the observations that the electron transport permitted by the interplay of photoassimilatory and photorespiratory electron transport is essential to prevent the photoinactivation of photosynthetic electron transport. The Mehler and Asada reactions, which give rise to strong nonphotochemical fluorescence quenching, are insufficient to protect the chloroplast electron transport chain against photoinactivation.     

Leaf chloroplast ultrastructure and photosynthetic properties of a chlorophyll-deficient mutant of rice

Leaf chloroplast ultrastructure and photosynthetic properties of a natural, yellow-green leaf mutant (ygl1) of rice were characterized. Our results showed that chloroplast development was significantly delayed in the mutant leaves compared with the wild-type rice (WT). As leaves matured, more grana stacks formed concurrently with increasing leaf chlorophyll (Chl) content. Except for the lower intercellular CO₂ concentration, the ygl1 plants had a higher leaf net photosynthetic rate, stomatal conductance, and transpiration rate than those of the WT plants. Under equal amounts of Chl, the excitation energy of PSI and PSII was much stronger in the mutant than that in the WT. The ygl1 plants showed higher nonphotochemical quenching and lower photochemical quenching. They also exhibited higher actual photochemical efficiency of PSII with a higher electron transport rate. Under the light of 200 μmol(photon) m^?2 s^?1, the ygl1 mutant showed lesser deepoxidation of violaxanthin in the xanthophyll cycle than WT, but it increased substantially under strong light conditions. In conclusion, the photosynthetic machinery of the ygl1 remained stable during leaf development. The plants were less sensitive to photoinhibition compared with WT due to the active xanthophyll cycle. The ygl1 plants were efficient in both light harvesting and conversion of solar energy.     

Characteristics of Photosynthetic Apparatus in Mn-Starved Maize Leaves

The effects of Mn-deficiency on CO₂ assimilation and excitation energy distribution were studied using Mn-starved maize leaves. Mn-deficiency caused about 70 % loss in the photon-saturated net photosynthetic rate (P _N) compared to control leaves. The loss of P _N was associated with a strong decrease in the activity of oxygen evolution complex (OEC) and the linear electron transport driven by photosystem 2 (PS2) in Mn-deficienct leaves. The photochemical quenching of PS2 (q_P) and the maximum efficiency of PS2 photochemistry (F_v/F_m) decreased significantly in Mn-starved leaves under high irradiance, implicating that serious photoinhibition took place. However, the high-energy fluorescence quenching (q_E) decreased, which was associated with xanthophyll cycle. The results showed that the pool of de-epoxidation components of the xanthophyll cycle was lowered markedly owing to Mn deficiency. Linear electron transport driven by PS2 de-creased significantly and was approximately 70 % lower in Mn-deficient leaves than that in control, indicating less trans-thylakoid pH gradient was built in Mn deficient leaves. We suggest that the decrease of non-radiative dissipation depending on xanthophyll cycle in Mn-starved leaves is a result of the deficiency of trans-thylakoid pH gradient.     

Variations in light energy dissipation in <Emphasis Type="Italic">Woodfordia fruticosa</Emphasis> leaves during expansion

Young leaves of tropical trees frequently appear red in color, with the redness disappearing as the leaves mature. During leaf expansion, plants may employ photoprotective mechanisms to cope with high light intensities; however, the variations in anthocyanin contents, nonphotochemical quenching (NPQ), and photorespiration during leaf expansion are poorly understood. Here, we investigated pigment contents, gas exchange, and chlorophyll (Chl) fluorescence in Woodfordia fruticosa leaves during their expansion. Young red leaves had significantly lower Chl content than that of expanding or mature leaves, but they accumulated significantly higher anthocyanins and dissipated more excited light energy through NPQ. As the leaves matured, net photosynthetic rate, total electron flow through PSII, and electron flow for ribulose-1,5-bisphosphate oxygenation gradually increased. Our results provided evidence that photorespiration is of fundamental importance in regulating the photosynthetic electron flow and CO₂ assimilation during leaf expansion.     

超高产杂交稻‘华安3号’冠层不同衰老程度叶片的光合功能

 较系统地研究了抽穗期超高产杂交稻‘华安3号’（`X075’×`紫恢100’）冠层顶部5片叶片的光合功能。结果表明,‘华安3号’剑叶的光系统Ⅱ（PSＩＩ）光化学最大效率(Fv/Fm)、开放的PSⅡ反应中心捕获激发能效率（Fv′/Fm′）、PSⅡ电子传递量子效率（ΦPSⅡ）、光化学猝灭系数（qP）、表观电子传递效率（ETR）、光合色素尤其是叶绿素（Chl）和类胡萝卜素（Car）中的新黄素、黄体素和β-胡萝卜素（β-Car）的含量等均优于其下的各叶,而PSⅡ的激发压力（1-qP）低于其它叶片。经对叶片低温（77K）荧光发射光谱的Gaussian解析,与其它各叶片相比,剑叶PSⅡ核心天线复合物CP47和光系统Ⅰ（PSⅠ）的含量较高,而非活性的PSⅡ捕光色素蛋白复合体（LHCⅡ）聚集态含量较少。研究证明：1）水稻在决定籽粒产量的生育后期,其干物质的积累主要是由冠层最上面的3片叶的光合作用所提供;2）在叶片衰老过程中,光合反应中心的衰老早于天线系统;3）杂交稻的光保护途径之一,可能在于光抑制条件下通过增加PSⅠ含量及其对光能的吸收并刺激环式电子传递高速运转,从而对光合器起保护作用;4）水稻叶片在衰老过程中,可能通过部分Chl b还原为Chl a,以降低LHCⅡ的含量,从而减少对光能的捕获,达到降低光抑制的伤害。