水淹对水芹叶片结构和光系统Ⅱ光抑制的影响

通过探讨在水淹条件下水芹（Oenanthe javanica）叶片结构的变化以及出水对其光系统II功能和光抑制的影响,阐明水芹光合机构在水淹条件下及出水后死亡的可能原因。结果表明：水淹条件下新生沉水功能叶光系统Ⅱ（PSⅡ）最大光化学效率（Fv/Fm）、电子传递活性与对照叶片差异很小,但水淹使气生功能叶的Fv/Fm显著降低;植株总生物量呈负增长趋势;活体弱光条件下,沉水叶出水后2小时叶片相对含水量（RWC）和Fv/Fm无显著变化;中等光强和强光条件下其RWC和Fv/Fm迅速降低;离体条件下,5小时的中等光强对沉水叶的Fv/Fm影响不显著,在随后的弱光下能恢复到出水时的初始状态;强光能使沉水叶的Fv/Fm大幅降低,且弱光下不能恢复到出水时的初始水平;在解剖结构上,水芹沉水叶的叶片总厚度、上下表皮厚度和气孔大小都显著低于气生叶,而且沉水叶没有明显的栅栏组织分化,但是沉水叶上表皮的气孔密度显著高于气生叶。研究结果表明,水淹使水芹原气生叶PSⅡ功能迅速衰退,但对新生沉水叶片影响很小。水芹植株出水后,沉水叶片结构变化使其在光下保水能力下降,而强光导致了光合机构的光抑制和反应中心失活。田间条件下两者共同作用则加剧了对叶片光合机构的破坏,进而致使其死亡。     

水淹导致皇冠草光合机构发生变化并加剧其出水后光抑制

通过气体交换和叶绿素荧光等方法研究了水淹及胁迫解除后皇冠草不同功能叶的光合特性及光抑制的变化.结果表明:与对照相比,气生叶(全淹组淹水前形成的功能叶)在水淹条件下叶片大小和气孔没有明显变化,但沉水叶(全淹组淹水后新生的功能叶)的叶面积增加,气孔变小,上表皮气孔密度增加.水淹导致气生叶碳同化能力、光化学效率和叶绿素含量下降.沉水叶在发育过程中碳同化能力、光化学效率和叶绿素逐渐升高.气生叶和沉水叶出水后其活体叶片在强光下的相对含水量急剧下降,发生明显的光抑制;而弱光下无明显光抑制发生.出水后离体叶片强光照射下6h后两种功能叶均发生严重光抑制,且弱光下不能恢复.因此,可以认为淹水条件下,沉水叶上表皮气孔密度的增加使其蒸腾速率提高;沉水叶较强的碳同化能力和增加的叶面积是确保其植株水下生存的重要因素;强光使气生叶和沉水叶出水后均发生严重光抑制,导度和蒸腾速率提高导致的叶片失水则加剧了这一过程,两者共同作用导致自然条件下两种功能叶的出水死亡.     

叶黄素循环和D1蛋白周转在毛竹叶片光保护中的作用

利用叶绿素荧光技术,对强光胁迫下以及叶黄素循环抑制剂-二硫苏糖醇(DTT)和D1蛋白合成抑制剂-硫酸链霉素(SM)处理后毛竹(Phyllostachys edulis (Carr.) Lehaie)的光抑制特征进行研究。结果显示:在夏季中午强光或人为强光胁迫下,毛竹叶片最大光化学效率Fv/Fm均显著降低;在下午光强减弱或黑暗、弱光条件下,Fv/Fm可有效恢复。DTT和SM均可抑制毛竹叶片非光化学淬灭(NPQ),且DTT效果明显优于SM。另外,在强光下,DTT和SM处理均能使毛竹叶片Fv/Fm、实际光化学效率Y(Ⅱ)和光化学淬灭qP等荧光参数下降幅度增大。研究结果表明毛竹叶片具有完善的光破坏防御机制,NPQ与叶黄素循环和D1蛋白周转紧密关联,在叶片光保护机制中具有重要作用。     

光强对砂仁叶片光合作用光抑制及热耗散的影响

通过测定不同光照条件下砂仁 (AmomumvillosumLour.)叶片气体交换和叶绿素荧光参数 ,探讨了光对其光合机构及其光破坏防御的影响。试验期间 ,上午 11:0 0之前有雾 ,光强较弱。上午砂仁阳生叶净光合速率 (Pn)与下午 (6 .5 3μmol·m-2 ·s-1)相似 ,高于阴生叶 (5 .94μmol·m-2 ·s-1) ,下午阴生叶Pn 高于上午 ,与阳生叶相似。下午砂仁叶片表观量子效率低于上午。其初始荧光 (Fo)、最大荧光 (Fm)、光系统Ⅱ (PSⅡ )最大光能转换效率 (Fv/Fm)、Fm/Fo 及PSⅡ的潜在效率 (Fv/Fo)随日光增强而降低 ,15 :0 0降至最低 ,表明光抑制逐渐加剧。之后随光强减弱这些叶绿素荧光参数升高 ,光抑制得到缓解。与此相反 ,非光化学猝灭系数 (qN)随光强的增加而升高 ,并一直维持在较高水平 ,表明依赖叶黄素循环的保护性反应逐渐增强。阳生叶的光抑制比阴生叶强烈 ,当日遮荫处理使光抑制缓解 ,但各处理间qN 差异不大 ,表明热耗散未受显著影响。结论 :弱光下砂仁叶片即发生光抑制 ,在不同光照下其光抑制的普遍发生 ,是依赖叶黄素循环的保护性反应 ,而非光破坏的结果 ;砂仁叶片叶黄素循环的启动不需过剩光能 ,不同光处理对其影响不大 ;砂仁对光的适应能力较强。     

热带雨林冠层树种绒毛番龙眼两种发育阶段叶片的光抑制

 通过测定西双版纳热带雨林冠层树种绒毛番龙眼(Pometia tomentosa)完全伸展嫩叶和成熟叶的叶片解剖、生理特征和雨季晴天自然条件下叶绿素a荧光以及午间强光对部分保护酶活性和膜脂过氧化作用的影响,探讨了两种不同发育阶段叶片光合作用的光抑制与强光和温度的关系。结果表明：绒毛番龙眼全展嫩叶和成熟叶表现出明显的解剖和生理特征差异。与全展嫩叶相比,成熟叶的叶片较厚、叶绿素含量高、气孔导度大、羧化效率高、最大净光合速率和光饱和点高,而气孔密度和保卫细胞长度没有显著差别。在雨季晴天自然条件下,午间最高光强可达2 200 μmol·m-2·s-1以上,最高叶温比气温高7～8 ℃,而成熟叶片的最高温度比全展嫩叶高1.5～2 ℃。上午随光强的增大,两种叶片的非光化学猝灭系数（NPQ）增大,PSⅡ原初光化学效率(Fv/Fm)、实际光化学效率［(Fm′_Fs)/Fm′］逐渐减小,在15∶30左右达最小。下午随着光强的减弱,Fv/Fm逐渐恢复,在傍晚基本恢复到清晨值。初始荧光(F0)在一天中变化很小。这表明绒毛番龙眼叶片光抑制是非辐射能量耗散增加引起的保护光合机构免受光破坏的保护性反应,而非光破坏。全展嫩叶比成熟叶有较低的光化学效率和非辐射耗散能力,对强光和高温处理的敏感性也较强,但在自然条件下一天中的光抑制程度与成熟叶没有显著差别。田间午间强光导致两种叶片的保护酶活性(超氧化物歧化酶,SOD;抗坏血酸过氧化物酶,APX)升高,而H2O2含量变化较小。其中,全展嫩叶的保护酶活性高,丙二醛(MDA)含量低。这表明自然条件下,与成熟叶相比,绒毛番龙眼全展嫩叶通过较低的光能利用效率、较低的叶温和高的保护酶活性减轻了强光高温的光抑制程度。     

高浓度CO2培养条件下极大螺旋藻光抑制研究

以极大螺旋藻作为实验材料,研究了不同CO2浓度培养对螺旋藻光抑制和恢复的影响,结果表明由光抑制导致的光合速率下降,高浓度CO2比低浓度CO2培养程度小,在高浓度CO2条件下培养的极大螺旋藻,虽然在强光下也表现出光抑制,但与低浓度CO2相比,光合速率下降得较慢。这种现象在强光与弱光培养均存在,但强光培养时更明显。光抑制后的恢复实验表明,不同CO2浓度培养的极大螺旋藻,光系统光化学活性(Fv/Fm)在弱光下恢复较好,高光强、高浓度CO2培养的藻,恢复速度稍快;而在黑暗中,几乎没有恢复;在弱光和含氯霉素的条件下Fv/Fm均下降。由此可见,高CO2浓度可减轻极大螺旋藻的光抑制,但对其光抑制后的恢复影响不大。       

短暂低温对佛手光合生理的影响

佛手(Citrus medica var. sarcodactylis Swingle)是一种对冷胁迫较为敏感的观果植物,在生产中普遍存在着冷害影响植物生长的现象.通过模拟浙中地区冬季设施种植中常见的短暂低温弱光条件,研究了佛手叶片的光合生理变化.研究表明,15℃低温即显著降低佛手光合速率、气孔导度,显著提高胞间CO2浓度;引起Fv/Fm显著性下降及初始荧光Fo显著上升的拐点温度为10℃,但延长处理时间至72h情况下,15℃亦显著降低Fv/Fm;低温处理还降低佛手光合羧化效率、最大光合速率,并导致光抑制现象发生时对应光强降低;低温条件下佛手叶片质膜透性及MDA含量高于对照,SOD、POD、CAT等抗氧化酶的活性则呈下降趋势;由此可见,短暂低温弱光胁迫首先是降低核酮糖1, 5-二磷酸羧化酶(Rubisco)等碳固定关键酶活性,引起氧自由基积聚,进而引发光抑制及光合速率的下降.     

高浓度CO_2培养条件下极大螺旋藻光抑制研究

以极大螺旋藻作为实验材料 ,研究了不同 CO2 浓度培养对螺旋藻光抑制和恢复的影响 ,结果表明由光抑制导致的光合速率下降 ,高浓度 CO2 比低浓度 CO2 培养程度小 ,在高浓度 CO2 条件下培养的极大螺旋藻 ,虽然在强光下也表现出光抑制 ,但与低浓度 CO2 相比 ,光合速率下降得较慢。这种现象在强光与弱光培养均存在 ,但强光培养时更明显。光抑制后的恢复实验表明 ,不同 CO2 浓度培养的极大螺旋藻 ,光系统 光化学活性 (Fv/Fm)在弱光下恢复较好 ,高光强、高浓度 CO2 培养的藻 ,恢复速度稍快 ;而在黑暗中 ,几乎没有恢复 ;在弱光和含氯霉素的条件下 Fv/Fm均下降。由此可见 ,高 CO2 浓度可减轻极大螺旋藻的光抑制 ,但对其光抑制后的恢复影响不大。     

早熟桃夏季叶色转红过程中的光化学响应特征

比较研究了‘早美’和‘春蕾’2个早熟桃品种夏季叶色转红对太阳光能的利用和光系统Ⅱ的叶绿素荧光特征的影响。结果表明：早熟桃叶片色素组成的变化会显著影响其光合和叶绿素荧光特性。叶色转红后,早熟桃净光合速率（Pn）日均值、PSII最大光化学效率（Fv/Fm）、PSII实际光化学效率（ФPSII）均上升,无显著光抑制,而绿叶对照‘红花碧桃’的电子传递速率（ETR）、Fv／Fm和ФPSII值均显著下降,7月光合明显受抑制。叶色转红程度较深的‘早美’在夏季高温强光下表现优于‘春蕾’和对照。淬灭分析表明：叶片花色素苷的积累能在短时间内增加PSII天线色素吸收的光能用于光化学反应的份额（P）与用于反应中心热耗散的相对份额（D）。转红后的叶片光化学淬灭系数（qp）显著高于绿叶,PSII光化学效率较高,但耗散过剩激发能的能力显著低于绿叶对照。     

苗期遮荫对花生（Arachis hypogaea L.）光合生理特性的影响

大田条件下,以花生品种"花育22号"为材料,齐苗期设置遮荫50%和85%两个遮荫强度分别处理40d,研究了遮荫对花生光合特性的影响及遮荫解除后的光合恢复规律.结果表明:(1)与正常光照条件相比,遮荫花生叶片净光合速率(Pn)、RuBP羧化效率降低,叶绿素含量、表观量子效率及光系统Ⅱ的最大光化学效率(Fv/Fm)增加,表明花生对弱光胁迫有一定的自我调节和适应能力.(2)遮荫和自然光下生长的花生中午强光下的Fv/Fm值均明显下降,表明发生了光抑制,遮荫程度越大,光抑制愈严重.(3)Fv/Fm值和净光合速率Pn遮荫解除后5d之内持续下降,之后逐步恢复.遮荫50%处理的叶片Fv/Fm值和Pn分别于遮荫解除后8d和10d左右恢复到对照水平;遮荫85%的处理分别于遮荫解除后15d和20d左右才恢复到最大,但Pn不能恢复到对照水平,显著低于对照.     

Xanthophyll Cycle and Inactivation of Photosystem Ⅱ Reaction Centers Alleviating Reducing Pressure to Photosystem Ⅰ in Morning Glory Leaves under Short-term High Irradiance

investigated through chlorophyll fluorescence parameters in morning glory (Ipomoea setosa) leaves, which were dipped into water, dithiothreitol (DTT) and lincomycin (LM), respectively. During the stress, both the xanthophyll cycle and D1 protein turnover could protect PSI from photoinhibition. In DTT leaves, non-photochemical quenching (NPQ) was inhibited greatly and the oxidation level of P700 (P700+) was the lowest one. However, the maximal photochemical efficiency of PSII (Fv/Fm) in DTT leaves was higher than that of LM leaves and was lower than that of control leaves. These results suggested that PSI was more sensitive to the loss of the xanthophyll cycle than PSII under high irradiance. In LM leaves, NPQ was partly inhibited, Fv/Fm was the lowest one among three treatments under high irradiance and P700+ was at a similar level as that of control leaves. These results implied that inactivation of PSII reaction centers could protect PSI from further photoinhibition. Additionally, the lowest of the number of active reaction centers to one inactive reaction center for a PSII cross-section (RC/CSo), maximal trapping rate in a PSII cross-section (TRo/CSo), electron transport in a PSII cross-section (ETo/CSo) and the highest of 1-qP in LM leaves further indicated that severe photoinhibition of PSII in LM leaves was mainly induced by inactivation of PSII reaction centers, which limited electrons transporting to PSI. However, relative to the LM leaves the higher level of RC/CSo, TRo/CSo, Fv/Fm and the lower level of 1-qP in DTT leaves indicated that PSI photoinhibition was mainly induced by the electron accumulation at the PSI acceptor side, which induced the decrease of P700+ under high irradiance.     

ABA对水稻幼苗叶片光抑制的光保护作用

经ABA处理的水稻幼苗叶片和对照相比 ,PSII光化学效率 (Fv/Fm)和非光化学猝灭系数 (qN)显著受抑制。经高光处理 1h后 ,ABA处理的水稻幼苗叶片光抑制程度比对照小 ,这暗示ABA对高光光抑制具有一定的光保护作用 ,且间接表明ABA提高水稻幼苗抗光抑制的能力与叶黄素循环密切相关。     

Increased photoinhibition in dehydrated leaves of hot pepper (Capsicum annuum L.) is not accompanied by an incremental loss of functional PSII

We examined the photosynthetic responses to photoinhibition in dehydrated leaves of hot pepper (Capsicum annuum L.). Stress was induced by immersing the roots of whole plants in Hoaglands solution containing polyethylene glycol (PEG) under high light (900 μmol photons m^-2 · s^-1). This PEG-treatment lowered the leaf water potential and the maximal rate of photosynthetic O₂ evolution (Pmax) linearly, in a time-dependent manner, to about 50% inhibition after 6 h. Pmax also decreased linearly as the period of high-light treatment lengthened. That inhibitory response was not as extreme, showing about 30% inhibition after 6 h. However, when the treatments of dehydration and high light were simultaneously administered, Pmax decreased more rapidly, in a synergistic fashion, showing about 90% inhibition within 2 h. Dehydration, in contrast to the light treatment, did not lower the maximal photochemical efficiency (Fv/Fm). Furthermore, this decline in Fv/Fm for light-treated, dehydrated leaves was almost identical to the response of photoinhibited leaves that were not dehydrated. Similar changes were observed in the number of functional PSII complexes. The decrease in Pmax and the amount of functional PSII was linearly correlated in photoinhibited leaves, but not in dehydrated leaves, regardless of light treatment. Therefore, we have demonstrated that exacerbated photoinhibition in dehydrated leaves occurs without an incremental loss of functional PSII.     

Effects of Strong Light and Active Oxygen on Photosynthesis in Soybean

With the use of chlorophyll fluorescence technique, it was found that the net photosynthetic oxygen evolution rate decreased after strong light (2 000 μmol· m-2·2-1 ) treatment for two hours in soybean ( Glycine max L. ) leaves. The chlorophyll fluorescence parameters, Fm/Fo, Fv/Fm, ФPSII, qp and qN decreased along with the increase of light intensity. In strong light, exogenous active oxygen H202、·OH and 'O2 were harmful to soybean leaves. The destruction of 'O2 and·OH to leaves was most evident, as was shown that Fv/Fm and PS H decreased significantly. The antioxidants DABCO, mannitol, ascorbate and histidine protected the leaves, but weakly, from strong light. In darkness, the SOD inhibitor sodium diethyldithiocar- bamate (DDC) had no significant effect on Fm/Fo and Fv/Fm, but NAN,, the ascorbate peroxidase (APX)inhibitor, significantly decreased Fm/Fo, Fv/Fm and ФPS II. In strong light, however, beth DDC and NaN3 reduced the above-mentioned fluorescence parameters, but NaN3 was more effective than DDC. The results suggested that photoinhibition did take place in soybean leaves under strong light, and it was related to active oxygen in vivo.     

Xanthophyll Cycle and Inactivation of Photosystem Ⅱ Reaction Centers Alleviating Reducing Pressure to Photosystem Ⅰ in Morning Glory Leaves under Short-term High Irradiance

Under 30-min high irradiance （1500μmol m^-2 s^-1）, the roles of the xanthophyll cycle and D1 protein turnover were investigated through chlorophyll fluorescence parameters in morning glory （Ipomoea setosa） leaves, which were dipped into water, dithiothreitol （DTT） and lincomycin （LM）, respectively. During the stress, both the xanthophyll cycle and D1 protein turnover could protect PSI from photoinhibition. In DTT leaves, non-photochemical quenching （NPQ） was inhibited greatly and the oxidation level of P700 （P700^＋） was the lowest one. However, the maximal photochemical efficiency of PSII （Fv/Fm） in DTT leaves was higher than that of LM leaves and was lower than that of control leaves. These results suggested that PSI was more sensitive to the loss of the xanthophyll cycle than PSII under high irradiance. In LM leaves, NPQ was partly inhibited, Fv/Fm was the lowest one among three treatments under high irradiance and P700^＋ was at a similar level as that of control leaves. These results implied that inactivation of PSII reaction centers could protect PSI from further photoinhibition. Additionally, the lowest of the number of active reaction centers to one inactive reaction center for a PSII cross-section （RC/CSo）, maximal trapping rate in a PSll cross-section （TRo/CSo）, electron transport in a PSll cross-section （ETo/CSo） and the highest of 1-qP in LM leaves further indicated that severe photoinhibition of PSII in LM leaves was mainly induced by inactivation of PSII reaction centers, which limited electrons transporting to PSh However, relative to the LM leaves the higher level of RC/CSo, TRo/CSo, Fv/Fm and the lower level of 1-qP in DTT leaves indicated that PSI photoinhibition was mainly induced by the electron accumulation at the PSI acceptor side, which induced the decrease of P700^＋ under high irradiance.     

Photoinhibition in cork-oak leaves under stress: influence of the bark-stripping on the chlorophyll fluorescence emission inQuercus suber L.

Quercus suber is the primary source for industrial cork and becomes bark-stripped every 9–10 years. Recurring cork extraction is a major stress factor and the large water loss from the stripped trunk surface may affect the water balance and tree productivity. To evaluate the effect of bark-stripping, fluorescence emission and stomatal conductance of leaves were determined in groups of bark-stripped and control trees. Fv/Fm ratio was found to be significantly lower in bark-stripped trees indicating a reduced photosynthetic efficiency of PSII. Photosynthesis was not found to be stomata limited. The reduction in Fv/Fm resulted from a decline in maximum and variable fluorescence while the initial fluorescence of the dark-adapted state (Fo) remained constant. A general decline in photosynthetic efficiency of PSII was found in all trees during the summer, probably reflecting the prolonged environmental stresses during a hot and dry season. Additional stress caused by the bark-stripping seems to enhance the susceptibility to photoinhibition of the trees.     

Post-illumination-related loss of photochemical efficiency of Photosystem II and degradation of the D1 protein are temperature-dependent

Photosystem II (PSII) photochemical efficiency (chlorophyll fluorescence ratio Fv/Fm) was recorded in vivo in Synechocystis 6803 during high light illumination and during a subsequent shift of the cells to darkness. A continuing decrease in the Fv/Fm ratio was observed even after the cells were transferred to darkness, provided the temperature was high enough. The decrease in the PSII efficiency after the shifting of the cells to darkness correlated directly with the loss of the D1 protein under different temperatures, suggesting that temperature-dependent proteolysis of the D1 protein in darkness induces the loss of PSII photochemical efficiency under these conditions. Furthermore, the amount of FtsH protease was found to increase during the high light treatment. This observation suggests that the synthesis of the FtsH protein is a light-regulated process and that this protease most probably has a key role in an efficient degradation of the D1 protein even under post-illuminative conditions, provided the temperature is high enough to prevent the initial reversible steps of photoinhibition.