Fluorescence Decay Studies of Chlorophyll a in Vivo

The study of the fluorescence of chlorophyll a offers a useful approach toward better understanding of the primary act of photosynthesis. This paper describes new measurements of the decay of chlorophyll a fluorescence in vivo, made with a considerably improved oscilloscopic-display technique. The main result is the identification of two decay periods both of the order of a few nanoseconds. Possible interpretations of this phenomenon are discussed.     

用体内叶绿素a荧光诱导动力学鉴定番茄的抗冷性

研究了冷害温度对具有不同抗冷性品种的番茄叶片的体内叶绿素a荧光诱导动力曲线的影响。实验结果指出,在低温处理(8℃,5℃,2℃下,暗中24小时)后,番茄叶片的体内叶绿素a荧光诱导动力学曲线有了明显的改变,Fv／Fo值、Rfd值降低了,光系统II原初光能转换效率和潜在的光合活力均受到抑制。我们在苗期和开花期得到的实验结果均表明,在番茄叶片的叶绿素a荧光诱导动力学曲线和这些荧光参数改变的程度与该品种的已知抗冷性之间呈现较好的相关性。我们认为,体内叶绿素a荧光诱导动力学方法是鉴定番茄抗冷性的一个快速、灵敏和可靠的方法,并可用于其他绿色植物的抗冷性鉴定中。     

Stimulation of Photophosphorylation by Ascorbate as a Function of Light Intensity

When isolated, stroma-free thylakoids are illuminated in the presence of ADP and orthophosphate in the absence of any electron acceptor except O2, the addition of ascorbate stimulates electron transport through the formation of the radical monodehydroascorbate and the coupled synthesis of ATP (G. Forti and G. Elli [1995] Plant Physiol 109: 1207-1211). The stimulation is shown here to be higher at low light intensity. These observations are explained in terms of the increase of the electron transport rate by ascorbate, which established a higher value of the steady-state pH gradient, causing activation of ATP synthase, which is known to be dependent on the level of the H+-electrochemical potential difference, and a higher rate of proton flux across the membranes available for utilization by ATP synthesis.     

文心兰浅绿条纹突变体的生理生化及叶绿素荧光特性研究

以文心兰浅绿条纹突变体为材料,分析叶片光合色素含量和组成、叶绿素合成前体物质含量以及叶绿素荧光参数的变化,观察突变体叶绿体超微结构的改变,以探寻其叶色变异的生理基础。结果表明:(1)突变体叶绿素a(Chl a)、叶绿素b(Chl b)、类胡萝卜素(Car)和总叶绿素(Chl)含量分别比叶色正常植株显著降低了37.1%、34.0%、30.8%和36.3%。(2)突变体叶绿素生物合成受阻于胆色素原(PBG)到尿卟啉原Ⅲ(UrogenⅢ)的反应步骤。(3)突变体叶绿体发育存在明显的缺陷,基粒数目及基粒片层的垛叠层数明显减少,嗜锇颗粒及囊泡较多。(4)突变体初始荧光(Fo)比正常植株高39%,最大荧光(Fm)、最大光化学效率(Fv/Fm)、PSⅡ有效光化学效率(Fv′/Fm′)和PSⅡ实际光化学效率(ΦPSⅡ)均显著低于正常植株,但光化学淬灭系数(qP)和非光化学淬灭系数(NPQ)与正常植株无显著差异。研究结果说明,文心兰叶绿素生物合成受阻和叶绿体结构发育不良,导致叶绿素的含量下降,致使突变体叶片呈现浅绿条纹,光能利用率降低。     

Growth and Ultrastructure of Rhodomicrobium vannielii as a Function of Light Intensity

Cells of Rhodomicrobium vannielii were grown in a controlled environment at several different light intensities. Differential rates of bacteriochlorophyll (BChl) synthesis and specific BChl contents were inversely related to the light intensity. On the other hand, the specific rate of growth-before reaching a maximal value-was directly related to the intensity of the light. Thin sections of cells grown at moderately low light showed the typical peripherally located, symmetrically distributed lamellate system, whereas an asymmetrical distribution of a less extensive lamellate system occurred in cells grown at high light intensities. It is proposed that a limited number of individual units of the lamellate system are originally derived from inward folds of the cytoplasmic membrane, and that subsequent lamellae arise by proliferation, including possible forking and definite folding back, of the few original lamellar membranes.     

Characteristics of Slow Induction Curve of Chlorophyll Fluorescence and CO2 Exchange for the Assessment of Plant Heat Tolerance at Various Levels of Light Intensity

The heat tolerance of wheat (Triticum aestivum L.) and radish (Raphanus sativus L. var. minor) cenoses exposed to elevated and damaging air temperatures (35°C for 20 h, 45°C for 7 h) under photoculture conditions at various levels of photosynthetically active radiation (PAR) was assessed by measuring characteristics of the slow induction curve of chlorophyll fluorescence at 682 and 734 nm and the CO₂ exchange rate. Irrespective of the illumination level, the exposure of the cenoses to 35°C did not induce irreversible changes in the plant photosynthetic apparatus. The lowest extent of damage to wheat and radish cenoses exposed to 45°C was observed at 150 W/m² of PAR, whereas the highest damage of the plants was observed at an illumination level that was close to the compensation point of the cenose photosynthesis (50–70 W/m² of PAR at air temperature of 24°C). Viability index proved to be the most sensitive characteristic, compared to other characteristics, which were determined by measuring the slow phase of fluorescence induction at 682 and 734 nm. In the cenoses studied, the pattern of changes in the viability index in response to a stress factor was close to the changes in the photosynthetic rate.     

蒙古栎和紫椴幼苗对光环境转变的光合作用响应

比较研究了从温室5%光强转到10%、30%和100%光强处理下,蒙古栎（Quercus mongolica）和紫椴（Tilia amurensis）幼苗的光合能力和叶绿素荧光的响应,揭示了两个树种对光环境变化的不同适应情况及其光保护机制。结果表明,光强转换后两种幼苗都发生了严重光抑制,蒙古栎幼苗的最大光化学效率（F_v/F_m）在光强转变后第3天降到最低（0.52）,紫椴幼苗在光强转变后第1天就降到了最低（0.67）,蒙古栎降低幅度明显高于紫椴。之后随着光适应时间的延长逐渐恢复到原有水平,说明短时期的光抑制没有对两种幼苗的光合机构造成光损伤;从不同光照条件来看,无论是最大净光合速率（P_max）,还是实际光化学效率（ФPSⅡ）,2种幼苗均为30%光强下的值高于10%和100%光强,说明过低或过高的光强都不利于幼苗的生长发育,只有适当的中光才利于幼苗的生长发育;与30%光强相比,蒙古栎幼苗100%光强下P_max、F_v/F_m、ФPSⅡ、NPQ的变化幅度远大于紫椴幼苗,表明高光强对蒙古栎幼苗的影响要大于紫椴;100%光强下,2种幼苗均通过大量增加非光化学淬灭（NPQ）、类胡萝卜素和叶绿素之比（Car/Chl）耗散过剩光能,降低单位鲜重叶绿素含量（Chl）以减少光能吸收,避免了光合机构光破坏。     

毛白杜鹃(Rhododendron mucronatum) 适生光强的生理生化研究

研究了毛白杜鹃最适生境的相对光强和其在不同相对光强生境中抗性变化的规律。结果表明：当生境的相对光强处于65％以上时,毛白杜鹃叶子内过氧化物酶和过氧化氢酶活性达到较低值,而还原型Vc,单宁酸,多酚类的含量达到了较高值。同时,在相对光强为65％以上的生境中,毛白杜鹃类不仅生长发育健壮,抗逆性强,而且,开花指数和观赏价值达到了较高值。因此,推断毛白杜鹃类适生生境的相对光强为65％以上。而且过氧化物酶和过氧化氢酶活性及还原型Vc、单宁酸、多酚类的含量可以作为衡量植物是否处于适生生境的指标。     

Predicting Light Acclimation in Cyanobacteria from Nonphotochemical Quenching of Photosystem II Fluorescence,Which Reflects State Transitions in These Organisms

An important factor in photosynthetic ecophysiology is the light regime that a photobiont is acclimated to exploit. In a wide range of cyanobacteria and cyano-lichens, the easily measured fluorescence parameters, coefficient of nonphotochemical quenching of photosystem II variable fluorescence (qN) and nonphotochemical quenching, decline to a minimum near the acclimated growth light intensity. This characteristic pattern predicts the integrated light regime to which populations are acclimated, information that is particularly useful for cyanobacteria or cyano-lichens from habitats with highly variable light intensities. qN reflects processes that compete with photosystem II photochemistry for absorbed excitation energy. In cyanobacteria, we find no evidence for energy-dependent quenching mechanisms, which are the predominant components of qN in higher plants. Instead, in cyanobacteria, qN correlates closely with the excitation flow from the phycobilisome to photosystem I, indicating that qN reflects the state transition mechanism for equilibration of excitation from the phycobilisome to the two photosystems.     

Evaluation of the Effect of Light Intensity on the Measurement of the Photosynthetic Rate in Plankton Microalgae by the Chlorophyll Fluorescence Method

The use of relative variable fluorescence (RVF) of chlorophyll, as measured in the presence of Diuron, an inhibitor of electron transfer, for the estimation of the photosynthetic activity of plankton microalgae was analyzed under a wide range of light intensities in the PAR region. Oxygen evolution rates (estimated by the method of light and dark bottles and the amperometric method), RVF, and chlorophyll a concentration were measured in parallel in natural algal cenoses and microecosystems. When the previously used regression equation, in the form A = b(F/F _d)C _chl I, where A is O₂ evolution rate (g/(m³ h), F/F _d is RVF (relative units), C _chl is chlorophyll a concentration (mg/m³), and I is light intensity (W/m²), was verified in the PAR region, we observed a nonlinear dependence of the correction coefficient b on I, which can be described by the formula b = 6.227 × 10³I. This result agrees with the hypothesis that chlorophyll a fluorescence quenching comprises photochemical (qQ) and energy (qE) components. On the basis of the energy model, we determined the upper limit b _max = 0.003 for light intensity range I< 4.4 W/m² and the lower limit b _min = 0.0003 for I = 400 W/m².     

Light-Induced Changes in the Fluorescence Yield of Chlorophyll a In Vivo: I. Anacystis nidulans

he fluorescence yield of chlorophyll a in dark adapted Anacystis nidulans undergoes a slow change with continuous illumination. After the completion of the initial fast transient, the fluorescence yield rises from the level S to a plateau M within a minute, declining only after prolonged illumination. Both normal and 1,1-dimethyl-3(3'4'-dichloro)-phenylurea (DCMU)-poisoned Anacystis are capable of these changes. In normal Anacystis, the slow increase in the fluorescence yield (S --> M) requires light absorbed in system II while light absorbed in system I is ineffective. In DCMU-poisoned Anacystis, however, these changes are also promoted by light absorbed in system I. Addition of carbonyl cyanide p-trifluoromethoxy phenylhydrazone (FCCP), a photophosphorylation uncoupler acting near the photosynthetic electron transport chain, abolishes the rise from S to M in normal but has no effect in the DCMU-poisoned system. Phlorizin, a phosphorylase inhibitor, has very little effect. These results suggest that the light-induced variation in the fluorescence yield is related to the conformational changes which accompany photophosphorylation. The fluorescence yield of the auxiliary pigment phycocyanin remains constant throughout the interval of the light-induced changes in the fluorescence yield of chlorophyll a. Consequently, the fluorescence spectrum of the alga is variable on continuous illumination.     

Light-Induced Changes in the Fluorescence Yield of Chlorophyll a In Vivo: II. Chlorella pyrenoidosa

The long-term fluorescence induction in Chlorella pyrenoidosa consists of a fast rise of the fluorescence yield from the level S (of the first wave transient) to a maximum M, followed by slower decay to a terminal stationary level T. The maximum M is attained within 40 seconds from the onset of illumination while the decay to the terminal level T lasts for several minutes. The fluorescence rise (S → M) coincides with an increase in the rate of oxygen evolution, which, however, remains constant during the fluorescence decay (M → T). Poisons of photosynthesis 3, (3,4-dichlorophenyl)-1,1 dimethylurea (DCMU, o-phenathroline) inhibit the fluorescence induction, while uncouplers of photophosphorylation affect the fluorescence time course only when they function at an early stage of the coupling sequence e.g., carbonyl cyanide p-trifluoremethoxy phenylhydrazone, (FCCP, atabrin). Phosphorylation inhibitors affecting only the terminal esterification step (phlorizin) have little effect on the fluorescence kinetics. These results suggest that the fluorescence induction requires the operation of a phosphorylating electron transport and that it is possibly related to the light-induced structural changes which accompany photophosphorylation.     

Light Gradients and the Transverse Distribution of Chlorophyll Fluorescence in Mangrove andCamelliaLeaves

The light gradient and transverse distribution of chlorophyllfluorescence in mangrove andCamellialeaves, which have differentmorphological characteristics, were examined using a micro-fluorescenceimaging system reported previously (Takahashiet al., Plant,Cell and Environment17: 105–110, 1994). Epidermal cellsscattered light strongly, resulting in an increase in the fluencerate in epidermal cells. For theCamellialeaf, a light gradientwas formed by absorption of light by photosynthetic pigmentsassociated with the induction of chlorophyll fluorescence. Forthe mangrove leaf, a light gradient was formed by backward scatteredlight within a thick layer of non-assimilatory cells. Lightwith a low absorption coefficient (515 nm) penetrated deeperthan that with a higher absorption coefficient (477 nm and 488nm) in theCamellialeaf, while light of both wavelengths showedsimilar profiles in the mangrove leaf. In the mangrove leaves,scattered light declined significantly in the non-assimilatorycell layer which is in front of the assimilatory cells. Light,the intensity of which was reduced to approx. 10% of the maximum,was well scattered and induced a considerable amount of chlorophyllfluorescence in the assimilatory cells, which appear to be wellorganized to capture weak light.Copyright 1998 Annals of BotanyCompany fluorescence, intact leaf, light gradient, mangrove (Rhizophora mucronataLamk.),Camellia japonicaL.     

Photoinhibition of Photosynthesis and in Vivo Chlorophyll Fluorescence in the Green Alga Ankistrodesmus braunii

The unicellular, green alga Ankistrodesmus braunii is subjectto a rapid photoinhibition of photosynthesis when exposed toa photon fluence rate in excess of that required to saturatephotosynthesis. Photoinhibition is manifested as a time-dependentdecrease in the capacity for either ¹⁴CO₂ fixation or CO₂-dependentO₂ evolution. Room temperature chlorophyll fluorescence inductionin intact cells, has been used to probe the primary site(s)of light damage during photoinhibition. Initially, at least,photoinhibition is due to a block in Photosystem II of photosyntheticelectron transport, at a site on the water-splitting side. (Received September 19, 1983; Accepted February 7, 1984)     

Light-Induced Changes in the Fluorescence Yield of Chlorophyll a In Vivo: III. The Dip and the Peak in the Fluorescence Transient of Chlorella pyrenoidosa

The fluorescence transient of Chlorella pyrenoidosa, excited by saturating light absorbed mainly by system II, has a dip D between the peak I at 75 msec and the large peak P at 400 msec (the times depend on light intensity). This dip is observed in aerobic cells and in anaerobic cells where it is prominent. In anaerobic cells, the I-D decline is hastened almost equally by absorption of either 705 or 650 nm background light. In anaerobic cells, supplementary 700 and 710 nm light given during the transient slightly hastens and heightens P. Methyl viologen, an exogenous system I electron acceptor, eliminates P. Results suggest that system I action causes D, and that P is due to reduction of Q (fluorescence quencher) and intersystem intermediates caused by development of a block in oxidation of XH (X being the primary electron acceptor of light reaction I). Mathematical analysis suggests that if only two forms of Q participate beyond I, then system I action is required for D. If three forms participate, then the system Q → QH → Q′ (see text) may explain D. The Malkin model (14), in its present form, does not allow D.     

Light-Induced Changes in the Fluorescence Yield of Chlorophyll a In Vivo: IV. The Effect of Preillumination on the Fluorescence Transient of Chlorella pyrenoidosa

The fluorescence transient of Chlorella pyrenoidosa, excited by saturating blue light, has a base level O, hump I, dip D, peak P, and at 1.5 sec a quasi-steady level S (12). With 2 sec exciting exposures and 4 min dark periods, preillumination-1 (lambda >/= 690 nm, intensities 1-750 ergs/sec-cm(2) incident), replacing the dark periods, lowers I more effectively than preillumination-2 (650 nm 相似文献   

强光胁迫对濒危植物金花茶幼苗生长和叶绿素荧光参数的影响

以当年生盆栽金花茶实生苗为材料,研究不同程度的强光胁迫（25％、50％和100％自然光强,以8%自然光强为对照）对其生长、生物量、叶片光合色素含量、叶绿素荧光参数的影响。结果表明：在不同程度的强光胁迫下,金花茶幼苗的生长均受到抑制,随着胁迫程度的增强,金花茶叶片颜色由深绿变为浅绿、黄绿色,叶片灼伤愈来愈严重;植株抽稍时间推迟,抽稍后长出的新叶长势较差;幼苗死亡率越来越高。幼苗根生物量、茎生物量、叶生物量和总生物量均随胁迫程度的升高而显著降低,强光胁迫对叶生物量的影响最大,根生物量次之,对茎生物量的影响最小。随着胁迫程度的增强,叶片叶绿素总量（Chl）、叶绿素a（Chla）、叶绿素b（Chlb）含量均显著降低,Chla/Chlb和Car/Chl显著升高。叶绿素荧光参数F_o、F_m、F_v、F_v/F_m、F_v/F_o均随胁迫程度的升高降低,强光胁迫使PSⅡ受到了伤害,光合作用原初反应过程受抑制,光合电子传递受到影响,从而抑制植株的正常生长。