Effect of long-term drought stress on leaf gas exchange and fluorescence parameters in C<Subscript>3</Subscript> and C<Subscript>4</Subscript> plants

A field study was performed on triticale, field bean, maize and amaranth, to find differences between studied species in physiological alterations resulting from progressive response as injuries and/or acclimation to long-term soil drought during various stages of plant development. The measurements of leaf water potential, electrolyte leakage, chlorophyll a fluorescence, leaf gas exchange and yield analysis were done. A special emphasis was given to the measurements of the blue, green, red and far-red fluorescence. Beside, different ratios of the four fluorescence bands (red/far-red: F ₆₉₀/F ₇₄₀, blue/red: F ₄₄₀/F ₆₉₀, blue/far-red: F ₄₄₀/F ₇₄₀ and blue/green: F ₄₄₀/F ₅₂₀) were calculated. Based on both yield analysis and measurements of physiological processes it can be suggested that field bean and maize responded with better tolerance to the water deficit in soil due to the activation of photoprotective mechanism probably connected with synthesis of the phenolic compounds, which can play a role of photoprotectors in different stages of plant development. The photosynthetic apparatus of those two species scattered the excess of excitation energy more effectively, partially through its transfer to PS I. In this way, plants avoided irreversible and/or deep injuries to PS II. The observed changes in the red fluorescence emission and in the F _v/F _m for triticale and amaranth could have occurred due to serious and irreversible photoinhibitory injuries. Probably, field bean and maize acclimatized more effectively to soil drought through the development of effective mechanisms for utilising excitation energy in the photosynthetic conversion of light accompanied by the mechanism protecting the photosynthetic apparatus against the excess of this energy.     

Photosynthetic activity of homoiochlorophyllous desiccation tolerant plant <Emphasis Type="Italic">Haberlea rhodopensis</Emphasis> during dehydration and rehydration

The functional state of the photosynthetic apparatus of flowering homoiochlorophyllous desiccation tolerant plant Haberlea rhodopensis during dehydration and subsequent rehydration was investigated in order to characterize some of the mechanisms by which resurrection plants survive drought stress. The changes in the CO₂ assimilation rate, chlorophyll fluorescence parameters, thermoluminescence, fluorescence imaging and electrophoretic characteristics of the chloroplast proteins were measured in control, moderately dehydrated (50% water content), desiccated (5% water content) and rehydrated plants. During the first phase of desiccation the net CO₂ assimilation decline was influenced by stomatal closure. Further lowering of net CO₂ assimilation was caused by both the decrease in stomatal conductance and in the photochemical activity of photosystem II. Severe dehydration caused inhibition of quantum yield of PSII electron transport, disappearance of thermoluminescence B band and mainly charge recombination related to S₂Q_A⁻ takes place. The blue and green fluorescence emission in desiccated leaves strongly increased. It could be suggested that unchanged chlorophyll content and amounts of chlorophyll–proteins, reversible modifications in PSII electron transport and enhanced probability for non-radiative energy dissipation as well as increased polyphenolic synthesis during desiccation of Haberlea contribute to drought resistance and fast recovery after rehydration.     

Effects of light quality on chlorophyll-forms Ca 684, Ca 690 and Ca 699 of the diatom Phaeodactylum tricornutum

Colored light modifies the relative concentration of chlorophyll-forms of the diatom Phaeodactylum tricornutum compared to white-light control. No change in the ratio carotenoids/chlorophylls was observed after 4 days exposure to green light (max: 530 nm), blue light (max: 470 nm) or red light ( > 650 nm) of same intensity.However, the absorption spectra were modified, the content in Ca 684, Ca 690, Ca 699 forms increased in red and green light cultures and photosynthetic unit size of PS II decreased by 30% in green and blue light cultures.Fluorescence emission and fluorescence excitation spectra according to the Butler and Kitajima method (1975) were carried out for each culture. Ca 669 form was predominant in the two photosystems. The newly appeared far red forms fluoresce at 715 nm like PS I forms.We conclude that these new forms originated in a rearrangement of PS II forms. They do not transmit excitation energy to reaction center of PS I and are disconnected from the other chlorophyll-forms of the photosynthetic antennae.Abbreviations ABS absorption - Ca chlorophyll-complex - chla chlorophyll a - chl c chlorophyll c - chl t total chlorophylls - D.C.M.U. 3-(3, 4 dichlorophenyl) 1-diméthyl-urea - d^v division - F fluorescence - PS I and PS II photosystem I and photosystem II     

Mycorrhizal impact on drought stress tolerance of rose plants probed by chlorophyll a fluorescence, proline content and visual scoring

Micropropagated rose plants (Rosa hybrida L., cv. New Dawn) were inoculated with the arbuscular mycorrhizal (AM) fungus Glomus intraradices (Schenk and Smith) and subjected to different drought regimens. The dual objectives of these experiments were to investigate the mechanism and the extent to which AM can prevent drought damages and whether physiological analyses reveal enhanced drought tolerance of an economically important plant such as the rose. In a long-term drought experiment with four different water regimens, visual scoring of wilt symptoms affirmed that AM in a selected host–symbiont combination increased plant performance. This effect was mostly expressed if moderate drought stress was constantly applied over a long period. In a short-term experiment in which severe drought stress was implemented and plants were allowed to recover after 4 or 9 days, no visual differences between mycorrhizal and non-mycorrhizal roses were observed. Therefore, the early physiological steps conferring drought tolerance were prone to investigation. Proline content in leaves proved to be an unsuitable marker for AM-induced drought tolerance, whereas analysis of chlorophyll a fluorescence using the JIP test (collecting stress-induced changes of the polyphasic O-J-I-P fluorescence kinetics in a non-destructive tissue screening) was more explanatory. Parameters derived from this test could describe the extent of foliar stress response and help to differentiate physiological mechanisms of stress tolerance. AM led to a more intense electron flow and a higher productive photosynthetic activity at several sites of the photosynthetic electron transport chain. A K step, known as a stress indicator of general character, appeared in the fluorescence transient only in drought-stressed non-mycorrhizal plants; conversely, the data elucidate a stabilising effect of AM on the oxygen-evolving complex at the donor site of photosystem (PS) II and at the electron-transport chain between PS II and PS I. If drought stress intensity was reduced by a prolonged and milder drying phase, these significant tolerance features were less pronounced or missing, indicating a possible threshold level for mycorrhizal tolerance induction.     

Comparison of light induced and cell cycle dependent changes in the photosynthetic apparatus: A fluorescence induction study on the green alga Scenedesmus obliquus

Changes in the photosynthetic apparatus occurring during the synchronous cell cycle of the green alga Scenedesmus obliquus are compared to the adaptational response induced by light intensity variations. To investigate and compare these two phenomena, we analyze the polyphasic rise of the chlorophyll fluorescence yield exhibited by plants and cyanobacteria when exposed to high intensity actinic light. Four fluorescence parameters are calculated which are closely related to Photosystem II (PS II) structure and function: ABS/RC, the antenna size of PS II; _PO, the quantum yield for reduction of the primary PS II quinone acceptor; q_PQ, related to the size of the plastoquinone pool; q_Emax, the capacity for pH dependent non-photochemical quenching. The capacity for non-photochemical quenching changes in response to light intensity variations, but it is not affected by the developmental changes occurring during the cell cycle. In contras t, for ABS/RC, _PO and q_PQ, we observe light induced as well as cell cycle dependent variations. We discuss the relations of the four fluorescence parameters to the molecular organization of the photosynthetic apparatus and its cell cycle and light dependent changes.     

干旱和复水对入侵植物三裂叶蟛蜞菊叶片叶绿素荧光特性的影响

选取入侵植物三裂叶蟛蜞菊(Wedelia trilobata)及其本地近缘种蟛蜞菊(W. chinensis)为实验材料,比较干旱和复水后二者叶片的叶绿素荧光特性和抗氧化酶活性等生理指标的变化规律,探讨入侵种三裂叶蟛蜞菊对干旱的响应和生态适应性.结果发现,在自然干旱处理过程中,入侵种三裂叶蟛蜞菊与本地种蟛蜞菊相比土壤含水量下降较快,对它们叶片气孔形态的比较发现,干旱胁迫11d后三裂叶蟛蜞菊叶片气孔开度明显大于蟛蜞菊,这可能是导致其失水较快的原因之一.干旱胁迫11d后三裂叶蟛蜞菊的PSⅡ最大光能转化效率(Fv/Fm)降低了43.8%,而蟛蜞菊只降低了3.7%;同时,与蟛蜞菊相比,三裂叶蟛蜞菊的PSⅡ实际光化学量子产量(Yield)、表观光合电子传递速率(ETR)和光化学猝灭系数(qP)也表现出较大幅度的降低,说明三裂叶蟛蜞菊对干旱胁迫较敏感;但复水后,三裂叶蟛蜞菊能够较快地恢复到正常水平,且与本地种不存在显著差异.这主要是由于入侵种在遭受干旱胁迫时提高了对其过量激发能的热耗散能力以及超氧化物歧化酶(SOD)和抗坏血酸还原酶(APX)的活性,保护光合机构少受不可逆的损伤,使其在干旱胁迫解除后光合功能得以迅速恢复.研究结果初步表明三裂叶蟛蜞菊容易受到水分条件的限制,它向干旱地区扩散的可能性较小.     

Weak red light plays an important role in awakening the photosynthetic machinery following desiccation in the subaerial cyanobacterium Nostoc flagelliforme

The subaerial cyanobacterium Nostoc flagelliforme can survive for years in the desiccated state and light exposure may stimulate photosynthetic recovery during rehydration. However, the influence of light quality on photosynthetic recovery and the underlying mechanism remain unresolved. Exposure of field collected N. flagelliforme to light intensity ≥2 μmol photons m⁻² s⁻¹ showed that the speed of photosystem II (PSII) recovery was in the following order: red > green > blue ≈ violet light. Decreasing the light intensity showed that weak red light stimulated PSII recovery during rehydration. The chlorophyll fluorescence transient and oxygen evolution activity indicated that the oxygen evolution complex (OEC) was the activated site triggered by weak red light. The damaged D1 protein accumulated in the thylakoid membrane during dehydration and is degraded and resynthesized during dark rehydration. PsbO interaction with the thylakoid membrane was induced by weak red light. Thus, weak red light plays an important role in triggering OEC photoactivation and the formation of functional PSII during rehydration. In its arid habitats, weak red light could stimulate the awakening of dormant N. flagelliforme after absorbing water from nighttime dew or rain to maximize growth during the early daylight hours of the dry season.     

Photosynthetic activity of poikilochlorophyllous desiccation tolerant plant <Emphasis Type="Italic">Reaumuria soongorica</Emphasis> during dehydration and re-hydration

Diurnal patterns of gas exchange and chlorophyll (Chl) fluorescence parameters of photosystem 2 (PS2) as well as Chl content were analyzed in Reaumuria soongorica (Pall.) Maxim., a perennial semi-shrub during dehydration and rehydration. The net photosynthetic rate (P _N), maximum photochemical efficiency of PS2 (variable to maximum fluorescence ratio, F_v/F_m), quantum efficiency of non-cyclic electron transport of PS2, and Chl content decreased, but non-photochemical quenching of fluorescence and carotenoid content increased in stems with the increasing of drought stress. 6 d after re-hydration, new leaves budded from stems. In the re-watered plants, the chloroplast function was restored and Chl a fluorescence returned to a similar level as in the control plants. This improved hydraulic adjustment in plant triggered a positive effect on ion flow in the tissues and increased shoot electrical admittance. Thus R. soongorica plants are able to sustain drought stress through leaf abscission and keep part of Chl content in stems.     

Physiological and biochemical tools useful in drought-tolerance detection in genotypes of winter triticale: accumulation of ferulic acid correlates with drought tolerance

BACKGROUND AND AIMS: The objectives of this study were to investigate whether a classification of triticale genotypes into drought-tolerant and drought-sensitive types based on field performance trials correlates with a classification based on measurements of some physiological and biochemical parameters in greenhouse conditions. In addition, an examination was carried out of whether ferulic acid, as the main origin of the blue fluorescence produced, contributes to drought tolerance. METHODS: Ten winter triticale genotypes were examined, five known to be drought tolerant and five drought sensitive. Measurements of the osmotic potential, leaf gas exchange, chlorophyll fluorescence, and blue and red fluorescence were performed. In addition, analysis of the total pool of phenolic compounds and ferulic acid as well as the measurements of PAL (l-phenylalanine ammonia-lyase) activity were carried out. KEY RESULTS: In agreement with field trials, three out of five cultivars ('Lamberto', 'Timbo' and 'Piano') were classified as drought tolerant. However, in the case of cultivar 'Babor', included in the group of drought-sensitive cultivars, the values obtained for some measured parameters were close to (F(v)(')/F(m)('), phenolics content, osmotic potential) or even better than (non-photochemical quenching, red and blue fluorescence, ferulic acid content) those for drought-tolerant genotypes. Cultivars 'Imperial', 'Ticino', 'Trimaran' and 'Boreas' were included in the drought-sensitive group, whereas cultivars 'Focus' and 'Kitaro' were included in the moderately sensitive group. CONCLUSIONS: The experiments confirmed that the period of flowering, the critical phase for plants as far as water demand is concerned, is suitable for plant screening and differentiation due to their tolerance to drought. The most important criteria which enabled creation of the ranking list of plants, from those sensitive to drought to those tolerant to drought, were the ability to perform the process of osmoregulation, the efficiency of the utilization of excitation energy by the photosynthetic apparatus and the functioning of protective mechanisms involving the level of ferulic acid in leaf tissues.     

干旱和复水对草莓叶片叶绿素荧光特性的影响

采用日本丰香草莓(Fragaria×ananassa Duch.cv.Toyonoka)品种进行实验,研究干旱和复水对其叶片叶绿素荧光特性的影响。结果表明,随着干旱胁迫程度的加剧,草莓叶片的最大荧光(Fm)、PSⅡ原初光能转化效率(Fv/Fm)、PSⅡ实际光化学效率(Yield)、光化学猝灭系数(qP)都随干旱胁迫的加剧而下降。干旱胁迫14d后,不同处理组草莓叶片的叶绿素荧光参数存在着显著的差异(P0.05)。复水后,低度胁迫和中度胁迫处理组能较快地恢复到正常水平,但重度胁迫组与对照组存在着显著的差异(P0.05)。     

Responses of the resurrection plant <Emphasis Type="Italic">Haberlea rhodopensis</Emphasis> to high irradiance

The effect of high irradiance (HI) during desiccation and subsequent rehydration of the homoiochlorophyllous desiccation-tolerant shade plant Haberlea rhodopensis was investigated. Plants were irradiated with a high quantum fluence rate (HI; 350 μmol m⁻² s⁻¹ compared to ca. 30 μmol m⁻² s⁻¹ at the natural rock habitat below trees) and subjected either to fast desiccation (tufts dehydrated with naturally occurring thin soil layers) or slow desiccation (tufts planted in pots in peat-soil dehydrated by withholding irrigation). Leaf water content was 5 % of the control after 4 d of fast and 19 d of slow desiccation. Haberlea was very sensitive to HI under all conditions. After 19 d at HI, even in well-watered plants there was a strong reduction of rates of net photosynthesis and transpiration, contents of chlorophyll (Chl) and carotenoids, as well as photosystem 2 activity (detected by the Chl fluorescence ratio R_Fd). Simultaneously, the blue/red and green/red fluorescence ratios increased considerably suggesting increased synthesis of polyphenolic compounds. Desiccation of plants in HI induced irreversible changes in the photosynthetic apparatus and leaves did not recover after rehydration regardless of fast or slow desiccation. Only young leaves survived desiccation.     

水分胁迫与复水对地枫皮生理生态特性的影响

以岩溶特有药用植物地枫皮为材料,研究土壤水分胁迫及复水条件下,其叶片光合参数、叶绿素荧光参数及光合色素含量的变化特性,进而探讨其对水分胁迫的生理生态适应性。结果表明:停止供水10 d,水分胁迫地枫皮叶片的P_n(净光合速率)、C_i(胞间CO_2浓度)、G_s(气孔导度)和L_s(气孔限制值)均下降,气孔限制是P_n降低的主要原因;停止供水15 d,水分胁迫地枫皮叶片的P_n日变化呈逐渐下降趋势,上午9:30以后全天的P_n值均接近零,非气孔限制成为P_n下降的主要因素;而对照地枫皮叶片的P_n日变化呈"双峰型",中午P_n下降的主要原因依然是气孔限制。水分胁迫下,地枫皮叶片叶绿素含量降低和Chl_(a/b)升高,减少了叶片对光能的捕获,减轻了光合机构遭受光氧化的破坏,而Car/Chl_(a+b)升高增强了光保护能力。水分胁迫下,地枫皮叶片的初始荧光(F_o)显著增大,最大荧光(F_m)、光系统Ⅱ(PSⅡ)潜在活性(F_v/F_o)和最大光化学效率(F_v/F_m)均显著降低,表明水分胁迫对地枫皮叶片的PSⅡ反应中心和电子传递造成了一定的破坏,从而使其PSⅡ的潜在活性和最大光化学效率降低。复水5 d后,地枫皮的上述生理生态参数均能恢复到对照水平,表明其复水后的生理修复能力很强。     

叶绿素延迟荧光的发生及其在光合作用研究中的应用

叶绿素延迟荧光主要由绿色植物中光系统Ⅱ的天线色素产生,光系统Ⅱ反应中心色素P680接受天线色素吸收的光能后转变为激发态的P680,P680回到基态时释放出一个电子传给原初电子受体,随后电子沿光合电子传递链向PSI传递。当进入电子传递链的电子发生电荷重组时会使P680再次激发形成P680,P680将激发能传递给天线色素后,激发能以荧光的形式释放出来,即为延迟荧光。延迟荧光的检测和分析技术为无损测定植物光合机构的结构与功能变化提供了新的方法。利用该方法可以获得丰富的光合机构信息,如光系统Ⅱ受体侧及供体侧的伤害程度、跨类囊体膜质子梯度的大小等。本文介绍了延迟荧光的产生原理和测定方法,并且举例说明了延迟荧光测定技术在光合作用研究中的应用。     

超表达拟南芥2-烯醛还原酶基因对烟草抗旱性的作用机理分析

为研究是否可以利用2-烯醛还原酶(AER)来清除活性氧下游的醛自由基达到提高植物的抗旱性,以超表达拟南芥AER基因烟草和野生型烟草(SR)为研究材料,利用干旱胁迫处理进行抗旱性分析,测定了干旱胁迫及复水后各个烟草株系的生物量、光合速率、叶绿素荧光参数、叶绿素含量、MDA和H2O2含量等指标。结果显示:(1)干旱胁迫下,转基因烟草株系的生物量、叶绿素含量、净光合速率、PSⅡ最大光化学效率及H2O2的清除能力均显著高于对照;(2)复水之后,烟草植株的各项生理指标都得到一定程度的恢复,而转基因株系相比于野生型恢复迅速,恢复能力更强。研究认为,超表达AER基因可以通过清除活性氧及其下游醛自由基来提高烟草的抗旱能力。     

Response of the photosynthetic apparatus of cotton (Gossypium hirsutum) to the onset of drought stress under field conditions studied by gas-exchange analysis and chlorophyll fluorescence imaging.

The functioning of the photosynthetic apparatus of cotton (Gossypium hirsutum) grown during the onset of water limitation was studied by gas-exchange and chlorophyll fluorescence to better understand the adaptation mechanisms of the photosynthetic apparatus to drought conditions. For this, cotton was grown in the field in Central Asia under well-irrigated and moderately drought-stressed conditions. The light and CO(2) responses of photosynthesis (A(G)), stomatal conductance (g(s)) and various chlorophyll fluorescence parameters were determined simultaneously. Furthermore, chlorophyll fluorescence images were taken from leaves to study the spatial pattern of photosystem II (PSII) efficiency and non-photochemical quenching parameters. Under low and moderate light intensity, the onset of drought stress caused an increase in the operating quantum efficiency of PSII photochemistry (varphi(PSII)) which indicated increased photorespiration since photosynthesis was hardly affected by water limitation. The increase in varphi(PSII) was caused by an increase of the efficiency of open PSII reaction centers (F(v)'/F(m)') and by a decrease of the basal non-photochemical quenching (varphi(NO)). Using a chlorophyll fluorescence imaging system a low spatial heterogeneity of varphi(PSII) was revealed under both irrigation treatments. The increased rate of photorespiration in plants during the onset of drought stress can be seen as an acclimation process to avoid an over-excitation of PSII under more severe drought conditions.     

Photoinhibition induced alterations in energy transfer process in phycobilisomes of PS II in the cyanobacterium, Spirulina platensis

Exposure of algae or plants to irradiance from above the light saturation point of photosynthesis is known as high light stress. This high light stress induces various responses including photoinhibition of the photosynthetic apparatus. The degree of photoinhibition could be clearly determined by measuring the parameters such as absorption and fluorescence of chromoproteins. In cyanobacteria and red algae, most of the photosystem (PS) II associated light harvesting is performed by a membrane attached complex called the phycobilisome (PBS). The effects of high intensity light (1000-4000 micromol photons m(-2) s(-1)) on excitation energy transfer from PBSs to PS II in a cyanobacterium Spirulina platensis were studied by measuring room temperature PC fluorescence emission spectra. High light (3000 micromol photons m(-2) s(-1)) stress had a significant effect on PC fluorescence emission spectra. On the other hand, light stress induced an increase in the ratio of PC fluorescence intensity of PBS indicating that light stress inhibits excitation energy transfer from PBS to PS II. The high light treatment to 3000 micromol photons m(-2) s(-1) caused disappearance of 31.5 kDa linker polypeptide which is known to link PC discs together. In addition we observed the similar decrease in the other polypeptide contents. Our data concludes that the Spirulina cells upon light treatment causes alterations in the phycobiliproteins (PBPs) and affects the energy transfer process within the PBSs.     

杨品种‘84K’光合生理的不同过程对干旱和复水的响应

以杨品种‘84K’（Populus alba×P.glandulosa）为材料,对其干旱胁迫及复水后光合生理特性的变化进行了研究。结果显示,在干旱胁迫及复水过程中,杨品种‘84K’光合作用相关的主要反应对此过程响应不同步。在干旱胁迫过程中,‘84K’的羧化反应速度、气孔导度（G_s）、叶肉导度（G_m）均显著下降,但前者下降幅度小于后两者,此时的光合作用主要受G_s和G_m制约。复水之后,G_m很快得到恢复,而光化学淬灭过程、羧化反应速度均没有恢复到对照水平,此时是光化学淬灭和（或）羧化反应制约了‘84K’的碳固定及光合作用。     

Physiological and biochemical parameters for identification of QTLs controlling the winter triticale drought tolerance at the seedling stage

The genetic map of the triticale is created on the basis of double-haploid (DH) lines, derived from F1 hybrids of a cross between the parental line Saka3006 and Modus. In order to localise drought resistance genes, it is necessary to find a phenotype feature which clearly differentiates between parental lines under drought stress conditions. With the future in mind, the aim of the presented studies was to analyse differences in the response to drought stress, between Saka3006 and Modus. Analyses of the water status of leaves, and the activity of the photosynthetic apparatus and protective mechanisms relating to the accumulation of phenolic compounds, were carried out. The studies were completed during the tillering phase.Statistically significant changes, between genotypes experiencing the drought period, were noticed for the osmotic potential, leaf water content, some parameters of chlorophyll fluorescence, and for phenolics and the ferulic acid content. On the basis of the studies, the Saka genotype can be considered drought resistant due to higher leaf water content caused, probably, by smaller hydraulic resistance relative to Modus. The activity of its photosynthetic apparatus during drought was higher than that for the Modus genotype. The high level of phenolic compounds, which can act as photoprotectors and free radical scavengers, was also maintained. All the mentioned parameters can represent the potential phenotype features, which allow the identification of resistance genes on the genetic map of the triticale, which is currently being created.     

Coupled cyclic electron transport in intact chloroplasts and leaves of C3 plants: Does it exist? if so,what is its function?

Transthylakoid proton transport based on Photosystem I-dependent cyclic electron transport has been demonstrated in isolated intact spinach chloroplasts already at very low photon flux densities when the acceptor side of Photosystem I (PS I) was largely closed. It was under strict redox control. In spinach leaves, high intensity flashes given every 50 s on top of far-red, but not on top of red background light decreased the activity of Photosystem II (PS II) in the absence of appreciable linear electron transport even when excitation of PS II by the background light was extremely weak. Downregulation of PS II was a consequence of cyclic electron transport as shown by differences in the redox state of P700 in the absence and the presence of CO₂ which drained electrons from the cyclic pathway eliminating control of PS II. In the presence of CO₂, cyclic electron transport comes into play only at higher photon flux densities. At H⁺/e=3 in linear electron transport, it does not appear to contribute much ATP for carbon reduction in C3 plants. Rather, its function is to control the activity of PS II. Control is necessary to prevent excessive reduction of the electron transport chain. This helps to protect the photosynthetic apparatus of leaves against photoinactivation under light stress.     

Three-stage Transformation of Chlorophyll Transient Fluorescence Pattern Under Sustained Dehydration and the Discovery of Critical Water Content in Seaweeds (in English)

The chlorophyll fluorescence kinetics of marine red alga Grateloupia turuturu Yamada, green alga Ulva pertusa Kjellm and brown alga Laminaria japonica Aresch during natural sustained dehydration were monitored and investigated. The pulse amplified modulation (PAM) system was used to analyze the distinct fluorescence parameters during thallus dehydration. Results proved that the fluorescence kinetics of different seaweed all showed three patterns of transformation with sustained water loss. These were: 1) peak kinetic pattern (at the early stage of dehydration fluorescence enhanced and quenched subsequently, representing a normal physiological state). 2) plateau kinetic pattern (with sustained water loss fluorescence enhanced continuously but quenching became slower, finally reaching its maximum). 3) Platform kinetic pattern (fluorescence fell and the shape of kinetic curve was similar to plateau kinetic pattern). A critical water content (CWC) could be found and defined as the percentage of water content just prior to the fluorescence drop and to be a significant physiological index for evaluation of plant drought tolerance. Once thallus water content became lower than this value the normal peak pattern can not be recovered even through rehydration, indicating an irreversible damage to the thylakoid membrane. The CWC value corresponding to different marine species were varied and negatively correlated with their desiccation tolerance, for example. Laminaria japonica had the highest CWC value (around 90%) and the lowest dehydration tolerance of the three. In addition, a fluorescence “burst” was found only in red algae during rehydration. The different fluorescence parameters Fo , Fv and Fv/ Fm were measured and compared during water loss. Both Fo and Fv increased in the first stage of dehydration but Fv / Fm kept almost constant. So the immediate response of in vivo chlorophyll fluorescence to dehydration was an enhancement. Later with sustained dehydration Fo increased continuously while Fv decreased and tended to become smaller and smaller. The major changes in fluorescence (including fluorescence drop during dehydration and the burst during rehydration) were all attributed to the change in Fo instead of Fv . This significance of Fo indicates that it is necessary to do more research on Fo as well as on its relationship with the state of thylakoid membrane.