外源胆固醇对水稻幼苗膜脂组成及抗冷力的影响

分析了水稻幼苗低温胁迫前后膜脂和膜脂脂肪酸含量变化。结果表明,经胆固醇处理的幼苗叶和根细胞膜脂中ＬＰＣ、ＰＳ和ＰＧ含量比对照下降,ＰＡ含量增加也较少。胆固醇处理的幼苗叶和根棕榈酸（１６：０）增加量和亚麻酸（１８：３）与ＩＵＦＡ减少量均明显比对照少。试验结果证明,水稻幼苗叶片和根系的抗冷力与ＰＡ含量和脂肪酸不饱和程度变化有密切关系。外源胆固醇处理水稻幼苗能阻止低温对膜脂的破坏作用,提高幼苗抗低温胁迫     

ABA对毛白杨抗冻性影响的研究

采用正交试验的方法设计了以ABA水溶液对毛白杨枝条进行水培的处理条件,并让每个处理接受两种低温条件,用电导法测定其伤害程度,得出冰冻1h和3h条件下的最佳水培条件为：ABA浓度30umol／L,无光照条件下水培2h。分别研究了脱落酸浓度、水培时间、水培光照条件对植物抗冻性的影响。     

桂花品种分类及木犀属种质资源的利用

在总结桂花栽培品种分类的基础上,根据桂花的开花季节、花色、花期、子房发育状况（能否结实）及营养器官等性状,既考虑品种进化关系和传统分类方法,又密切结合生产实际的需要,提出了桂花品种分类的五级标准。并对木犀属的地理分布和种质资源的利用进行了讨论。     

抗冻糖蛋白溶液中冰晶生长速率的研究

在分析了溶液中抗冻糖蛋白与冰晶表面的相互作用的基础上,提出了在抗冻糖蛋白溶液中冰晶沿c轴方向生长的理论。给出了冰晶在抗冻糖蛋白溶液中生长速率的定量计算,而且理论值与实验结果有较好的符合,解释了冰晶在抗冻糖蛋白溶液中生长速度和生长习性的各向异性。     

基于AFLP分子标记的桂花品种核心种质的构建

用100个桂花品种荧光AFLP分子标记信息构建核心种质。利用获得的指纹信息,运用UPGMA聚类取样法,采用Kimura 2-parameter遗传距离,多次聚类随机抽样。结果表明:(1)8对引物共获得514条带,平均每对引物获得64条带。(2)从100个桂花品种中筛选了30个样本的核心种质。(3)比较核心种质和全部种质的Shan-non-Wiener指数(H′)和Simpson指数(D),t检验值均说明核心种质的遗传多样性指数与全部种质遗传多样性没有明显差异,表明所构建的核心样品能够很好地保留原始100个桂花品种的遗传多样性。     

植物抗冻机理研究新进展：抗冻基因表达及其功能

综述了迄今业已分离和鉴定的低温诱导表达的抗冻基因,以及通过染色体基因制图方法揭示和证实的抗冻性基因。并着重地介绍了这些抗冻基因在提高植物抗冻能力上的功能。这些抗冻基因表达合成的新多肽具有高度的亲水性,起着保护和稳定细胞膜结构的作用,从而防止冰冻伤害、提高植物的抗冻能力。同时还介绍了抗冻基因表达中的某些调节因子,其中尤其值得注意的是,CBF基因似乎有可能作为抗冻基因表达的“主开关”,以及Ca2+作为植物细胞的第二信使在传递低温信号、启动和调节抗冻基因表达中可能的重要作用。这些研究结果,不仅为阐明植物的抗冻机理提供了新的证据,而且为改良农作物的抗寒性提供了新的启示。     

ABA诱致叶绿体膜脂变化和脂褐素类似物积累

酰脂是叶绿体膜结构的主要组分,它们的种类和在膜上的分布与膜的功能有关(Rawyler和Siegenthaler 1980)。Henry等(1982)曾证明,叶绿体在体外老化时膜的半乳糖脂和磷脂的相对含量发生变化。ABA一般能加速叶片的衰老反应,它在叶片衰老时积累(Wright和 Hiron 1970)。在气孔开启状态下,激动素有防止衰老的效应(Thimann和Satler 1979)。在衰老的菜豆(Pha-     

厦门市桂花病虫害种类及防治

1998~2004年对厦门市桂花病虫害进行系统调查,查明桂花病虫害10种,其中病害6种,虫害4种;文中提出这些病虫害的防治方案。     

抗冻蛋白特征、作用机理与预测新进展

抗冻蛋白（antifreezeproteins,AFPs）可以通过抑制冰晶生长保护生物体免受低温冻害,具有重要的生物学意义和应用价值。现在在鱼类、节肢动物、植物及微生物中均发现有AFPs的存在。基于对已有研究文献和相关网络数据的系统调查统计,详细描述了AFPs数据的类别特征,并对其作用机理的研究历史和最新取得的突破性进展作了较为系统的阐述,并对AFPs预测所取得的成果作了介绍,还对AFPs研究的现状和未来研究方向作了讨论和展望。     

丹桂和籽银桂花芽分化的研究

采用石蜡切片技术,对不育的丹桂（Osmanthus fragrans ‘Dangui’）和可育的籽银桂（Osmanthus fragrans ‘Ziyingui’）花芽分化的过程进行了研究。结果表明,桂花（Osmanthus fragrans Lour.）花芽形态分化可分为花芽分化初始期、总苞分化期、花原基分化期、顶花花被分化期、雄蕊分化期和雌蕊分化期6个阶段。雄蕊的发育在丹桂和籽银桂之间基本没有区别,都能形成完整的花粉囊和成熟的花粉粒。但是,雌蕊的发育在可育的籽银桂与不育的丹桂之间存在明显差异。根据花芽分化的过程证明,丹桂的不育是由于雌蕊发育不正常导致的。     

中国桂花的研究历史、现状与桂花品种国际登录

简要回顾了中国桂花(Osmanthus fragrans Lour．)的研究历史,对桂花品种研究的现状和存在的问题进行了评述,介绍了申报桂花品种国际登录工作的意义和目前的工作进展。桂花品种的现代分类始于20世纪80年代,除了传统的形态分类以外,同工酶、分子标记等技术已用于桂花品种亲缘关系的研究中,但目前仍缺乏合理的品种分类原则和分类系统,品种调查、记载和命名比较混乱,因此应加强桂花品种形态学的基础研究。     

江西全南古桂和野生桂花资源调查

桂花[ Osmanthus fragrans(Thunb.)Lour.]为木犀科(Oleaceae)木犀属(Osmanthus Lour.)植物,是中国传统十大名花之一,已有2 500余年的栽培历史.桂花是一个长寿树种,在中国很多地方都有树龄上百年甚至上千年的古桂存在[1]18,[2].中国是世界上桂花古树保存最多、分布最广、最集中的国家[1]20.古桂不仅具有文物价值和旅游价值,还具有重要的科研价值,是研究古气候、古环境、古树种质资源以及新品种培育的绝好材料[3].     

福建长汀石峰寨景区桂花次生林群落物种数量特征

对福建省长汀县石峰寨风景区桂花[Osmanthus fragrans (Thunb.)Lour.]次生林群落的上坡位、中坡位、下坡位和整个坡面的群落种类组成、重要值和物种多样性等研究表明,该桂花次生林群落各坡位的物种特征有一定差别;群落立地单元不同,其优势度和均匀度也不同;中坡位的立地条件最优,群落优势度最小;桂花在上坡位的重要值最大;桂花对严酪自然环境的适应能力较强。     

Comparison of exportation and metabolism of xylem-delivered ABA in maize leaves at different water status and xylem sap pH

³H-ABA was introduced into the xylem stream of maize ( Zea mays}) leaves on intact plants by incubation of a semi-attached flap of the sheath in solutions. The relative contribution of exportation and metabolism to the fate of xylem-delivered ABA was assessed in leaves which were either kept at different water potentials through soil drying treatments or subjected to different xylem pHs (pH 7.4 vs. pH 5.5) through a phosphate buffer in the feeding solutions. Xylem-delivered ABA was rapidly metabolised in well-watered leaves with a half-life of 2.19 h in the relatively mature leaves used in this study. Re-exportation of xylem-delivered ABA from leaves was much slower than metabolism. It took 24 h for half of the fed radioactivity to disappear from the well-watered leaves, and very possibly this radioactivity was in the form of metabolites of fed ³H-ABA. Although soil drying usually increases the output of ABA through phloem as reported in previous studies, it greatly reduced the re-exportation of xylem-fed ABA and/or its metabolites. Metabolism was also significantly reduced by the treatment of soil drying (half-life extended from 2.19 to 3.63 h), although the magnitude of change was much less than that of exportation. Manipulation of the pH in the feeding solution also had its effect on the re-exportation. A shift of pH from 5.5 to 7.4 reduced the rate of disappearance of the total radioactivity fed into the attached leaves, but showed no significant effect on the rate of ABA metabolism. It was concluded that it was the ABA metabolism, rather than a re-exportation from leaves, which was mainly responsible for the disposal of the ABA signal from the xylem and therefore preventing an accumulation in leaves. Water stress and pH increase of xylem sap would increase the time of such ABA's presence in the leaves. Since xylem-imported ABA is unlikely to be re-exported from leaves in its intact form, we believe a recycling of ABA from xylem to phloem through leaves plays only a minor role.     

Cell biological mechanism for triggering of ABA accumulation under water stress in Vicia faba leaves

Water stress-induced ABA accumulation is a cellular signaling process from water stress perception to activation of genes encoding key enzymes of ABA biosynthesis, of which the water stress-signal perception by cells or triggering mechanism of the ABA accumulation is the center in the whole process of ABA related-stress signaling in plants. The cell biological mechanism for triggering of ABA accumulation under water stress was studied in leaves of Vicia faba. Mannitol at 890 mmol · kg-1 osmotic concentration induced an increase of more than 5 times in ABA concentration in detached leaf tissues, but the same concentration of mannitol only induced an increase of less than 40 % in ABA concentration in protoplasts. Like in detached leaf tissues, ABA concentration in isolated cells increased more than 10 times under the treatment of mannitol at 890 mmol · kg-1 concentration, suggesting that the interaction between plasmalemma and cell wall was essential to triggering of the water stress-induced ABA accumula     

Novel approaches for examining the effects of differential soil compaction on xylem sap abscisic acid concentration, stomatal conductance and growth in barley (Hordeum vulgare L.)

Novel techniques were devised to explore the mechanisms mediating the adverse effects of compacted soil on plants. These included growing plants in: (i) profiles containing horizons differing in their degree of compaction and; (ii) split-pots in which the roots were divided between compartments containing moderately (1·4 g cm ^{? 3}) and severely compacted (1·7 g cm ^{? 3}) soil. Wild-type and ABA-deficient genotypes of barley were used to examine the role of abscisic acid (ABA) as a root-to-shoot signal. Shoot dry weight and leaf area were reduced and root : shoot ratio was increased relative to 1·4 g cm ^{? 3} control plants whenever plants of both genotypes encountered severely compacted horizons. In bartey cultivar Steptoe, stomatal conductance decreased within 4 d of the first roots encountering 1·7 g cm ^{? 3} soil and increased over a similar period when roots penetrated from 1·7 g cm ^{? 3} into 1·4 g cm ^{? 3} soil. Conductance was again reduced by a second 1·7 g cm ^{? 3} horizon. These responses were inversely correlated with xylem sap ABA concentration. No equivalent stomatal responses occurred in Az34 (ABA deficient genotype), in which the changes in xylem sap ABA were much smaller. When plants were grown in 1·7 : 1·4 g cm ^{? 3} split-pots, shoot growth was unaffected relative to 1·4 g cm ^{? 3} control plants in Steptoe, but was significantly reduced in Az34. Excision of the roots in compacted soil restored growth to the 1·4 g cm ^{? 3} control level in Az34. Stomatal conductance was reduced in the split-pot treatment of Steptoe, but returned to the 1·4 g cm ^{? 3} control level when the roots in compacted soil were excised. Xylem sap ABA concentration was initially higher than in 1·4 g cm ^{? 3} control plants but subsequently returned to the control level; no recovery occurred if the roots in compacted soil were left intact. Xylem sap ABA concentration in the split-pot treatment of Az34 was initially similar to plants grown in uniform 1·7 g cm ^{? 3} soil, but returned to the 1·4 g cm ^{? 3} control level when the roots in the compacted compartment were excised. These results clearly demonstrate the involvement of a root-sourced signal in mediating responses to compacted soil; the role of ABA in providing this signal and future applications of the compaction procedures reported here are discussed.     

蔓三七叶中分离绿原酸和异绿原酸及其抗氧化活性研究

以蔓三七叶为原料,制备其中的绿原酸和异绿原酸A、B和C,并对它们进行结构鉴定;同时,采用DPPH法、水杨酸比色法、邻苯三酚自氧化法来对其进行体外抗氧化活性研究。结果表明,分离制备的绿原酸和异绿原酸A、B和C质量分数分别为96. 8%、98. 2%、97. 6%和98. 7%。在0. 5～10μg/mL范围内,绿原酸和异绿原酸A、B和C对DPPH和羟基自由基表现出了较好的清除作用,随浓度升高而逐渐增大;但它们对超氧自由基的清除作用时,浓度从5μg/mL升高到100μg/mL时,清除作用都未出现明显的剂量依赖性,各样品与阳性对照组(VC)相比较而言,其清除超氧自由基的作用明显较弱。本文揭示了蔓三七叶中的绿原酸和异绿原酸A、B和C具有不同的抗氧化效果。     

Induction of freezing tolerance in potato (Solanum commersonü) suspension cultured cells

The induction of freezing tolerance by abscisic acid (ABA) or cold treatment in suspension cultured cells of Solanum commersonii was studied. Both ABA (50–100 μ M ) at 23°C and low temperature (4°C) increased freezing tolerance in cultured Solanum commersonii cells from a LT₅₀ (freezing temperature at which 50% cells were killed) of —5°C (control) to —11.5°C in 2 days. Cold-induced freezing tolerance reached its maximum at 2 days and remained constant throughout the cold acclimation period of 11 days. The freezing tolerance induced by ABA, however, showed a rapid decline 2 to 5 days after initiation of ABA treatments. Addition of ABA (100 μ M ) to the culture medium at the inception of low temperature treatment did not enhance freezing tolerance of the cells beyond the level attainable by either treatment singly. Poly(A⁺)-RNA was isolated from the respective treatments, translated in a rabbit reticulocyte lysate cell free system, and the translation products were resolved by two dimensional polyacrylamide gel electrophoresis (ID-PAGE). Analysis of the in vitro translated products revealed changes in the abundance of approximately 26 products (encoding for polypeptides with M, of 14 to 69 kDa and pl of 4.90 to 6.60) in ABA-treated cells 12 h after treatment, and 20 (encoding for polypeptides with M_r of 12 to 69 kDa, with pl of 4.80 to 6.42) in cells exposed to 4°C for 12 h. There were only 5 novel translation products observed when the ABA-treated cells reached the highest level of freezing tolerance (2 days after the initiation of ABA treatment). Changes in translatable RNA populations during the induction of freezing tolerance in cells treated with either ABA or low temperature are discussed.