不同叶色矢竹叶绿体结构和光系统特性差异

以矢竹(Pseudosasa japonica)、花叶矢竹(P. japonica f. akebonosuji)和曙筋矢竹(P. japonica f. akebono)为研究对象, 借助叶绿体超微结构和荧光动力学曲线的变化揭示不同叶色矢竹的光系统活性及光合特性差异。结果表明: 3个竹种的光合色素含量差异明显, 除花叶矢竹条纹叶白色部分叶绿体内无完整类囊体片层结构外, 花叶矢竹绿条纹和曙筋矢竹的基粒数明显少于矢竹, 叶绿体发育成熟度不一致; OJIP曲线及参数表明, 花叶矢竹条纹绿叶和曙筋矢竹光系统II (PSII)反应中心开放降低程度低于矢竹, 捕获能量用于电子传递的份额变小, PSII活性变弱; 而曙筋矢竹叶片P700至初级电子受体(Q_A)的电子传递链氧化还原平衡偏向于还原侧, 推测其光系统I (PSI)反应中心P700至PSII Q_A电子传递链受损。因此, PSII活性变化导致叶绿体发育不成熟, 可能是引起矢竹类叶色差异的直接原因。     

光响应曲线的指数改进模型与常用模型比较

光响应曲线的参数是研究植物生理状态的重要指标, 常用的光响应曲线模型无法准确地计算出光饱和点和最大净光合速率。该文利用光响应曲线新模型——指数改进模型、直角双曲线模型、直角双曲线修正模型、非直角双曲线模型和指数模型, 拟合高粱(Sorghum bicolor)、苋(Amaranthus tricolor)、大麦(Hordeum vulgare)和半夏(Pinellia ternata)的光响应曲线, 并随机选取部分数据进行检验, 得到了各模型计算出的主要生理参数, 并对这些数据进行了比较分析, 讨论了各模型之间的优缺点和准确性, 描述了C₃、C₄植物光响应的适宜性。结果表明, 基于C₃植物得到的指数改进模型和直角双曲线修正模型能较准确地计算出C₃、C₄植物饱和光强和最大净光合速率, 并在描述光响应曲线时比另外3个模型具有更高的精确性和适宜性。实验结果可为光响应曲线模型在C₃和C₄光合途径植物中的应用提供参考。     

土壤水、氮供应对麻疯树幼苗光合特性的影响

在盆栽半控制试验中, 采用两因素的随机区组设计, 在3个土壤水分梯度(分别为80%、50%和30%的田间持水量(FC))下研究了施氮肥和不施氮肥处理麻疯树(Jatropha curcas)幼苗的光合特性。比较了不同水分和氮素供应条件下麻疯树幼苗的光合-光响应和CO₂响应曲线、PSII的最大光化学效率(F_v/F_m)、氮含量和光合色素含量之间的差异。结果表明: 1)施氮肥处理中, 随着土壤水分含量的增加, 叶片表观量子效率(AQY)、光补偿点、最大净光合速率、羧化效率、光呼吸速率、暗呼吸速率和叶片氮含量均呈现增加的趋势, 而且均在80% FC下最高。2)不施氮肥处理中, 随着土壤水分含量的增加, 麻疯树各光合参数均与施氮肥处理呈现相反的变化趋势。3)在30% FC下, 施氮肥处理和不施氮肥处理相比, 氮含量显著增加, AQY、F_v/F_m、光合色素含量无显著的变化, 其他各项指标均显著降低。这些结果表明, 水氮耦合效应对麻疯树光合特性有显著影响, 尤其是在80% FC下增施氮肥的效果最为明显。因此, 在土壤氮素含量不高的情况下, 麻疯树更适宜在较低的土壤水分下生长, 土壤水分较高反而不利于麻疯树的光合作用; 而如果增施氮肥, 麻疯树在土壤水分含量较高时生长更好。     

指数改进模型在大麦光合-CO2响应曲线中的适用性

光合-CO₂响应曲线是研究植物对CO₂响应的重要工具。常用的光合-CO₂响应曲线模型, 除直角双曲线修正模型外, 均无法准确地计算出CO₂饱和点和光合能力。该文利用新的指数改进模型拟合大麦(Hordeum vulgare)光合-CO₂响应曲线, 与直角双曲线修正模型、直角双曲线模型、指数模型、非直角双曲线模型进行比较, 并随机选取部分数据进行检验, 同时得到了各个光合-CO₂响应曲线模型的主要生理参数, 对这些数据进行了比较分析, 讨论了各模型之间的优缺点和准确合理性。结果表明, 指数改进模型在5个模型中具有最好的精确度和合理性, 能准确地描述出大麦的光合-CO₂响应曲线, 计算出CO₂饱和点为484 μmol∙mol^-1, 光合能力为25.9 μmol CO₂∙m^-2∙s^-1。     

民勤沙生植物园4种云杉属植物光化学特性的趋同适应

采用叶绿素荧光图像分析手段,结合叶绿素含量和主枝生长量测定,研究了沙地云杉、青海云杉、蓝云杉、白扦PSⅡ光化学效率和非光化学能量耗散的光响应特性及对稳态光强的适应性。结果表明:在相同生境和管理条件下,15a苗龄的4种云杉属植物生长势态良好,均能适应民勤荒漠气候环境;蓝云杉针叶的叶绿素含量较高,而青海云杉的叶绿素a、b比值(Chl a/b)较低;4种植物PSⅡ光化学效率的光响应曲线相似,但蓝云杉PSⅡ非光化学猝灭系数(NPQ)的光响应明显有别于其余3种;150μmol m~(-2)s~(-1)低光强下4种植物间NPQ的差异与PSⅡ最大光化学量子效率(Fv/Fm)一致,是内禀光合特性的反映;1500μmol m~(-2)s~(-1)高光强下的NPQ和PSⅡ最大效率(Fv'/Fm')在4云杉属植物间没有差异,呈现光合生理的趋同适应。综合比较分析可知,蓝云杉和白扦在低光强具有略低的PSⅡ非光化学猝灭能力,在高光强具有相对高的PSⅡ运行效率(Fq'/Fm'),光驯化适应能力较大;沙地云杉和青海云杉具有几乎一致的PSⅡ光化学和非光化学猝灭特性,其耐荫性和喜光性相近;4种云杉属植物光合机构对干旱荒漠生境的驯化适应具有趋同性,可作为我国北方防护林建设和城市绿化的重要树种。     

落叶松幼苗光合特性对氮和磷缺乏的响应

为探讨落叶松幼苗光合特性对氮、磷营养缺乏的响应规律,在温室内用砂培方法培养和处理落叶树幼苗,测定了净光合速率和叶绿素荧光等反映其光合能力的参数,分析了落叶松幼苗的光合特性对氮、磷营养缺乏的响应规律.结果表明,氮素供应不足(1mmol·L^-1)时,落叶松幼苗针叶的全氮含量、叶绿素含量和净光合速率与对照相比都显著降低,分别下降了37%、31%和59%,同时,F_v/F_m(反映光系统II最大光能转换效率)和F_v/F_o(反映光系统II潜在活性)也分别下降了22%和57%,而叶片可溶性蛋白含量只有微弱下降.磷素供应不足(1/8mmol·L^-1)时,叶片全氮和全磷含量、叶绿素含量、叶片可溶性蛋白含量和F_v/F_m与对照相比差异均不显著,净光合速率和F_v/F_o下降13%.氮、磷同时缺乏时,上述各项指标的变化与单独缺氮处理的相似,这意味着本实验中缺磷处理(1/8mmol·L^-1)对落叶松幼苗光合特性影响相对较小.     

淹水胁迫对星花玉兰及其品种光合特性的影响

为探究星花玉兰（Yulania stellata）光合生理特性对淹水胁迫的响应规律,采用双套盆法对星花玉兰及其4个品种进行淹水处理,测定不同淹水时间叶绿素含量、比叶面积、光合参数和叶绿素荧光参数的变化。结果表明：①在淹水胁迫下,各品种叶绿素a、叶绿素b和总叶绿素变化趋势基本一致,‘皮鲁埃特’和‘菊花’未出现显著性变化,星花玉兰、‘贝蒂’和‘朱迪’呈下降趋势。②各品种的净光合速率（P_n）呈下降趋势,处理组最大净光合速率（P_nmax）与光饱和点（L_SP）均显著低于对照组;‘菊花’和‘皮鲁埃特’的暗呼吸速率（R_d）为处理组高于对照组,而‘贝蒂’、‘朱迪’和星花玉兰的Rd在淹水处理后显著降低,光合产物消耗减少。③各品种星花玉兰的最大光化学量子产量（F_v/F_m）均为下降趋势。‘皮鲁埃特’与‘朱迪’有效光化学量子产量（Φ_PSⅡ）在淹水胁迫下整体下降幅度较小,分别为8.4%和24.7%;‘菊花’、‘贝蒂’和星花玉兰则下降幅度较大,分别为76.7%、85.7%和64.6%。淹水胁迫影响星花玉兰及其品种光合特性,不同品种有差异,除‘贝蒂’外其余4个星花玉兰品种在处理前7 d时光合作用正常进行,‘皮鲁埃特’具有较强的光合能力和涝害适应能力。研究结果可为筛选适应南方湿涝地区或易积水地区栽植的星花玉兰品种提供理论依据。     

青藏高原东缘林线交错带糙皮桦幼苗光合特性对模拟增温的短期响应

采用开顶式生长室(OTC)模拟增温对植被影响的研究方法, 研究了青藏高原东缘林线交错带糙皮桦(Betula utilis)光合特性对模拟增温的响应。结果表明: 与对照样地相比, OTC内日平均气温(1.2 m)在植物生长季中增加2.9 ℃, 5 cm土壤温度增加0.4 ℃。增温使糙皮桦幼苗叶片的净光合速率(P_n)、蒸腾速率(T_r)和气孔导度(G_s)分别增加17.4%、21.4%和33.9%, 但对糙皮桦幼苗叶片的水分利用率(WUE)却没有明显影响, 而对糙皮桦的叶氮浓度却表现为显著的负效应。同时, 增温能显著增加糙皮桦幼苗的最大同化速率(P_nmax) (+19.6%)、暗呼吸速率(R_d) (+14.3%)、表观量子效率(AQY) (+7.9%), 但对其光补偿点(LCP)和光饱和点(LSP)却没有明显的影响。此外, 增温使糙皮桦幼苗叶片的最大羧化速率(V_cmax)和电子传递速率(J)分别增加了12.3%和11.7%, 而磷酸丙糖利用率(TPU)和CO₂补偿点(CCP)对增温却并不敏感。该研究表明, 模拟增温对林线糙皮桦光合生理总体上表现为正效应, 这有可能帮助该物种对未来气候变化更快更好地适应。     

田间条件下棉花幼叶光合特性及光保护机制

通过比较棉花(Gossypium hirsutum)幼叶和完全展开叶气体交换参数及叶绿素荧光特性的差异, 探讨高光强下幼叶的光抑制程度及明确光保护机制间的协调机理。在田间自然条件下, 以棉花刚展平的幼嫩叶片(幼叶)和面积已达到最大的完全展开叶片为研究对象, 通过测定不同发育阶段叶片气体交换参数及叶绿素a荧光参数的变化, 并运用Dual-PAM100对不同发育阶段的叶片进行快速光响应曲线的拟合。结果表明: 幼叶和完全展开叶片在光合、荧光特性方面表现出明显的差异。与完全展开叶相比, 较低的叶绿素(Chl)含量和气孔导度(G_s)是幼叶较低净光合速率(P_n)的限制因素, 从而直接导致其光系统II (PSII)实际光化学效率(Φ_PSII)和光化学猝灭系数(q_P)的降低。在1800 μmol·m^-2·s^-1光强以下, 完全展开叶具有较强的围绕PSI循环的电子流(CEF), 有利于合成ATP, 是其具有较高光合能力的原因之一。相同光强下, 幼叶较低的光饱和点(LSP)更易受光抑制, 但其PSII原初光化学效率(F_v/F_m)的日变化幅度显著小于完全展开叶, 说明强光下幼叶通过类胡萝卜素(Car)猝灭单线态氧、光呼吸(P_r)、热耗散(NPQ)以及PSI-CEF等光保护机制能有效地耗散过剩的光能, 从而避免其光合机构发生光抑制。     

胡杨异形叶光合作用对光强与CO2浓度的响应

胡杨(Populus euphratica)叶形多变, 随个体生长发育, 植株出现条形、卵形和锯齿阔卵形叶。在新疆塔里木河上游人工胡杨林内选择具有此3种叶形的成年标准株, 将枝条拉至同一高度, 通过活体测定, 比较其光合作用-光与CO₂响应及叶绿素荧光响应特征。结果表明: 胡杨异形叶光合速率对光强/CO₂浓度与电子传递速率对光强的响应曲线均可用直角双曲线修正模型来拟合, 得出的主要光合参数与实测值较吻合。胡杨卵形叶、锯齿阔卵形叶光合速率-光响应参数与生化参数及快速光响应参数与条形叶差异显著, 而光合速率-CO₂响应参数则无显著差异。胡杨异形叶CO₂饱和浓度下的最大净光合速率(P_nmax)较饱和光强下的P_nmax高, 表明胡杨强光下光合速率在很大程度上受CO₂供应和1,5-二磷酸核酮糖(RuBP)再生能力的限制。卵形叶、锯齿阔卵形叶的初始量子效率(α)、初始羧化效率(CE)、P_nmax、光合能力(A_max)与最大羧化速率(V_cmax)均显著高于条形叶; 锯齿叶光饱和点(LSP)、最大电子传递速率(ETR_max)与光呼吸速率(R_p)高于卵形叶, 条形叶光补偿点(LCP)与LSP、α、CE最低。表明荒漠干旱环境下胡杨锯齿叶最耐强光, 高R_p可能是其耗散过剩光能、保护光合机构免于强光破坏的重要途径; 卵形叶高的α、CE、磷酸丙糖利用效率(TPU)、PSII实际光化学效率(Φ_PSII)与低LCP及叶氮分配策略是其保持高光合速率的原因; 条形叶Φ_PSII、ETR、P_n低, 因其制造光合产物不足而难以满足树体生长逐渐减少并处于树冠下部。可见, 胡杨条形叶光合效率低、抗逆性差, 主要以维持生长为主; 随着树体长大, 条形叶难以适应荒漠环境来维系其生长, 出现了卵形叶; 卵形叶光合效率高, 易于快速积累光合产物而加快树体生长, 但其LSP低和耐光抑制能力弱, 逐渐被更耐强光、高温与大气干旱的锯齿叶所取代, 从而使胡杨在极端逆境下得以生存, 这是胡杨从幼苗到成年叶形变化及异形叶着生在树冠不同高度的原因。     

Further research on chemotaxonomy of paeonol and analogs in Paeonia (Ranunculaceae)

In this paper, the paeonol, paeoniflorin and their analogs were analyzed in the roots of 14 species and 2 subspecies of Paeonia L. The existence and content of these compounds were discussed in three sections, sect. Moutan, sect. Paeonia and sect. Onaepia. In sect. Moutan, paeonol and its analogs were high in content in all species. In sect. Paeonia, low content of paeonol and its analogs were found in plants of four taxa, P. lactiflora, P. anomala ssp. veitchii, P. mairei and P. intermedia. None of these compounds was found in sect. Onaepia. Paeonol has a simple structure and is distributed widely in plant; its decrease and loss may be the result of evolution. Therefore, it is deduced that the relationship among the three sections of Paeonia might be that woody sect. Moutan is the more primitive and derived from the ancestor of Paeonia first. For the herbaceous sections, sect. Paeonia is more closely related to sect. Moutan than to sect. Onaepia. In sect. Moutan, there are less paeonol and its analogs in the species of subsect. Vaginata than in those of subsect. Delavayanae. Thus, the former may be considered more advanced. In sect. Paeonia, the taxa with minor content of paeonol and its analogs are diploid except P. mairei. Among them, P. lactiflora and P. anomala ssp. veitchii are relatively primitive by morphology. None of paeonol and its analogs was detected in the species with specialized form.     

Photosynthetic characteristics of leaves of male-sterile and hermaphrodite sex types of Plantago lanceolata grown under conditions of contrasting nitrogen and light availabilities

Plantago lanceolata is a gynodioecious species: In natural populations male steriles (MS) coexist with hermaphrodites (H). Since male steriles have a reproductive disadvantage, without any compensation for their loss in male function by an increase in female function, they are expected to disappear from the population. In this study we investigated the possibility that differences in ecologically important photosynthetic characteristics, between MS and H lines of P. lanceolata. play a role in maintaining gynodioecy. One MS line and two H lines were grown under conditions of high N and light availability, as well as under either N limitation or light limitation, to investigate whether the sex types respond differently to environmental constraints. Photosynthetic light-response and CO₂-response curves were made, together with leaf organic N and chlorophyll determinations. There were only few small differences between the lines and since the MS line did not differ in any of the determined photosynthetic characteristics from either H line, it is unlikely that these differences are involved in maintaining male sterility in populations of P. lanceolata. The low-light-grown plants showed a high degree of acclimation as shown by a two-fold higher leaf area to leaf weight ratio (SLA), a two-fold higher investment of N in light harvesting, and higher net photosynthetic rates under low-light conditions, as compared to the high-light-grown plants. The low-N-grown plants used their organic N more efficiently in photosynthesis compared to plants grown at an optimal N supply. This was mainly due to the N-limited plants having leaves with a lower organic N content and thus lower photosynthetic capacities. To a lesser extent it was due to the higher value for the curvature factor of the light-response curves of the N-limited plants, to their decreased rates of photorespiration and possibly to their relatively higher allocation of organic N to photosynthetic functions.     

白芍传统品种原植物遗传多样性及亲缘关系分析

为探讨白芍原植物各居群间的遗传多样性及亲缘关系,本实验应用RAPD技术,使用40条随机引物对10个白芍原植物居群的叶片总DNA进行PCR扩增。结果表明：白芍10个原植物居群间具有较丰富的遗传多样性,多态率达63．以％。由结合线L＝0．7975可将10个居群划分为6组,原植物为芍药(Paeonia lactiflora Pall.)的6个居群中有4个居群集中在第3组,显示了种内遗传关系的相似性,其中川白芍(芍药)花色有变,同时雄蕊有部分辨化的现象,与野生种(韩城芍药)有较远的遗传关系;山东荷泽居群雄蕊全部瓣化,种质可能来自于观赏芍药突变体,在遗传关系上与芍药的其他居群有一定的距离。原植物为毛果芍药[P.lactiflora var.trichocarpa (Bunge) Stern]的4个居群中,杭白芍粉红花居群和白花居群独立成一组,与形态分类的结果一致。芍药及其变种毛果芍药的遗传关系非常近,但是有交叉。因此形态分类和遗传关系应综合考虑,作为种下分类单位的确定也应慎重。     

Paeonia in Xinjiang,China

The present paper deals with the genus Paeonia in Xinjiang, whose taxonomy has been confused. Based on the field observation, population sampling and the examination of herbarium specimens, a taxonomical revision is made in this paper. Two species are recognized, i. e. Paeonia anomala L. and P. sinjiangensis K. Y. Pan. P. altaica K. M. Dai et T. H. Ying is reduced to P. sinjiangensis and P. hybrida (= P. anomala var. intermedia) is reduced to P. anomala. The diagnostic characters of the two species are described and illustrated, and a map of their distribution in Xinjiang is presented. A key to these two species is provided here. 1. Roots straight, not thickened; sepals all caudate, less frequently one or very rarely two non-caudate ................................................ 1. P. sinjiangensis K. Y. Pan. 2. Roots fusiform or tuberous; inner three sepals non-caudate, less frequently one of them caudate .............................................................. 2. P. anomala L. key words Xinjiang; Paeonia; P. anomala; P. sinjiangensis; revision     

传统中药白芍原植物分类鉴定及根形态解剖研究

对我国主产地的白芍(Radix Paeonia alba)原植物10个居群进行调查及标本采集,植物鉴定结果为：川白芍原植物粉红花居群为原变种芍药Paeonia lactiflora Pall,白花居群为芍药变种毛果芍药P.lactiflora var.trichocarpa(Bunge)Stern;毫白芍原植物线条居群和蒲棒居群均为芍药;杭白芍原植物红花、白花、粉红花居群均为毛果芍药;陕西韩城、江苏东海、山东荷泽白芍均为芍药,各居群在花色及形态上有明显而稳定的变异。根横切面解剖结构显示,按木质部的排列方式可将白芍原植物10个居群分为两大类：第一类为有呈两个不相连的扇形中央导管群,并且有狭长、具分枝的从形成层到根中央部分连续排列的木质部,基本上是原植物芍药的植物特征,其中毫白芍线条居群兼有毛果芍药和芍药的特征;第二类为具有不明显的根中央扇形导管束,导管束呈环状围绕中央排列,并且有粗短不分枝的靠近形成层处成群的导管,与原植物毛果芍药的特征基本一致,其中杭白芍红花居群与川白芍白花居群根中央导管群呈现较明显的2个分离扇形排列,类似芍药。白芍原植物的种分类定位与花色无密切关联,但由于性状的稳定,可以考虑作为变种或变型定位。     

Photosynthetic light-response curves

The shapes of photosynthetic light-response curves for leaves of Eucalyptus maculata (Hook) and E. pauciflora (Sieber ex Sprengel) were examined. Three different methods were used to measure photosynthesis: CO₂ and H₂O-vapour exchange, O₂ evolution at a 5-kPa CO₂ partial pressure, and chlorophyll fluorescence. The three methods were compared and gave good agreement when measured under equivalent conditions. However, O₂ evolution was inhibited by high CO₂ partial pressures. A non-rectangular hyperbolic curve has been used widely to describe photosynthetic light-response curves. It has three variables which define the maximum quantum yield (photosynthetic rate divided by absorbed irradiance at very low irradiances), the maximum capacity and the curvature (Θ). We found that Θ was affected by the CO₂ partial pressure, declining to a minimum of about 0.6 as CO₂ partial pressure increased to 100 Pa. Further increases in the CO₂ partial pressure began to inhibit the rate of O₂ evolution at 2000 μmol quanta · m^?2·^?1 and Θ increased back to 0.95 by 5 kPa CO₂ partial pressure. At low irradiances, photosynthesis is limited by the rate of electron transport while at high irradiances, photosynthesis is frequently limited by the activity of ribulose-1,5-bisphosphate carboxylase-oxygenase (Rubisco). The dependence of Θ on CO₂ partial pressure arises because the transition between limitations changes as a function of the CO₂ partial pressure. The light-response curve is truncated by the transition to a Rubisco limitation and the lower the irradiance at the transition, the higher the value of Θ. There is a gradient in light absorption through the leaf which influences the photosynthetic capacity of different layers within the leaf. The gradient in photosynthetic capacity can be demonstrated by the fact that the shape of the light-response curve changes when the leaf is illuminated unilaterally onto either the adaxial or abaxial surface. We compared two Eucalyptus species which had either isolateral or dorsiventral leaf anatomy. Leaves were able to reverse completely the gradients in photosynthetic capacity following inversion of the leaves for a week, irrespective of their anatomy.     

Molecular phylogenetic evidence for the origin of a diploid hybrid of Paeonia (Paeoniaceae)

There is growing evidence that hybridization not only by means of allopolyploidy but also at the homoploidy level was a major driving force of plant diversification. While allopolyploidy is known to be a common mode of speciation in Paeonia (Paeoniaceae), hybrid speciation at the diploid level needs further evaluation. Paeonia anomala was previously considered to be an interspecific hybrid but with an unknown ploidy level. In this study P. anomala is identified as a diploid (2n = 10). With increased sampling of populations and molecular markers, we showed that P. anomala is a homoploid hybrid that originated from a cross between P. veitchii and P. lactiflora. Five populations of P. anomala were sequenced for the following molecular markers: the matK gene and two intergenic spacers, psbA-trnH and rps16-trnQ, of the chloroplast genome; the internal transcribed spacers (ITS) of nuclear ribosomal DNA; and three low-copy nuclear genes, Adh1, Adh2, and Gpat. The populations of P. anomala were grouped together with P. veitchii on the ITS and Gpat phylogenies but with P. lactiflora on the chloroplast phylogeny. Sequence polymorphism was found at the Adh1 and Adh2 loci within individuals of P. anomala. These polymorphic sequences were grouped with P. veitchii and P. lactiflora, respectively. Phenetic analysis indicated that P. anomala is morphologically similar to P. veitchii. Phenotypic evolution resulting from the combination of two diverged genomes might have occurred primarily at the physiological level and allowed P. anomala to adapt to geographic regions different from those of its parents.     

Cd2+胁迫对银芽柳PSⅡ叶绿素荧光光响应曲线的影响

以盆栽银芽柳为材料,利用MINI-IMAGING-PAM荧光成像测定系统,研究了Cd²⁺胁迫下叶片叶绿素荧光参数的变化及其光响应曲线。结果表明,初始荧光Fo与最大荧光Fm随着Cd²⁺浓度的增大而呈现先升后降的趋势,Fo与Fm在200 mg/LCd²⁺处理4周时达到最高值,400 mg/LCd²⁺处理则显著下降;PSⅡ最大光化学效率(Fv/Fm)与PSⅡ潜在光化学效率(Fv/Fo)显著受 Cd²⁺胁迫抑制,但随Cd²⁺浓度的增加呈先降后升的变化趋势。Cd²⁺胁迫下各叶绿素荧光参数的光响应结果表明,PSⅡ实际光量子效率Y(Ⅱ)、荧光淬灭系数(qP)随光化光强度的增加呈下降趋势,而同光强下高浓度Cd²⁺ 使Y(Ⅱ)与(qP) 显著降低;PSⅡ调节性能量耗散的量子产额Y(NPQ)、非光化学淬灭系数(qN)与表观电子传递速率(ETR)则随着光强增加呈上升趋势,同光强下高浓度Cd²⁺处理显著提高Y(NPQ)、qN 与ETR。Cd²⁺胁迫下,PSⅡ非调节性能量耗散的量子产额Y(NO)稳定在较低水平,同光强下Y(NO)随Cd²⁺浓度增加略有提高。说明,银芽柳通过调节PSⅡ反应中心开放程度与活性,对Cd²⁺胁迫表现出较强的耐性,高浓度Cd²⁺胁迫导致PSⅡ反应中心关闭或不可逆失活,表现出光抑制。     

The Early Development of Embryo and Endosperm of Paeonia lactifiora

The present paper reports the early development of embryo and endosperm of Paeonia lactiflora. The main conclusions are as follows: 1 The zygote nucleus divides directly to form a coenocytic proembryo with different number of free nuclei. The result confirms the conclusion of Yakovlev[6] as well as Yakovlev and Yoffe[7] On the occurnce of coenocytic proembryo in Paeonia suffruticosa Andr. (P. moutan Sims), P. albiflora Pall. (P. lactiflora Pall), P. officinalis L., P. tenuifolia L., P. anomala L., P. veitchii Lynch (P. beresowskii Komarov), P. wittmanniana, also it agrees with the report of Cave et al.[4] on the occurence of the coenocytie proembryo in Paeonia californica and P. brownii. From the result of our investigation, there is no basis to support Murgai's conclusion obtained in certain species of Paeonia, i.e., the first division of zygote nucleus is accompanied by wall formation and the coenocyte is a suspensor. The primary endosperm nucleus of P. lactiflora divides often earlier than zygote nucleus, or almost at the same time or later in a few cases; 2 Both mitosis and amitosis occur in the free nuclei in the coenocytic proembryo, and mitosis is dominant. In the later stage of development the amitosis occurs at the micropylar region of the coenocytic proembryo, in the free nuclear endosperm at the chalazal region and the appressed part of the chalazal end of the coenocytic proembryo. In addition, in the region of conenocytic proembryo and endosperm polyploid nuclei, irregular nuclei are also frequently met with; 3 Cell wall formation in the coenocyte and the endosperm initiates by means of both cell plate and freely growthing walls, but in the coenocyte wall formation is earlier than in the free nuclear endosperm. At first, wall formation of the coenocytic proembryo begins at the chalazal end, and then extends toward the micropylar region, and in endosperm it begins at the part appressed to the part of the chalazal end of coenocytic proembryo, and then extends toward the chalazal end. We support Cave’s suggestion of the parallel evolution for Paeonia possessed the coenocytic proembryo has no relation to the coenocytic proembryo of the gymnosperms. Further we consider the evolution tendency of the coenocytic proembryo of Paeonia toward a functional specialization.