春化温度对大白菜花芽分化和抽薹的影响

以冬性有明显差异的 6个大白菜品种为试材 ,研究了 4个春化温度对大白菜的花芽分化和抽薹的影响 .结果表明 ,弱冬性材料在 3～ 11℃范围内 ,花芽分化和抽薹均能在较短的时间完成 ;强冬性材料适宜的春化温度为 3～ 7℃ ,超过 7℃ ,花芽分化和抽薹急剧延迟 ;冬性中等材料适宜的春化温度为 3～ 9℃ .故一般采用 3～ 7℃的春化温度对不同冬性材料均适宜     

温度对叶用莴苣春化的影响

为了探讨温度对叶用莴苣春化的影响,进而明确其春化类型,本试验选用两个易抽薹叶用莴苣品种GB-30和GB-31为试材,分别进行20 d的4、20和25 ℃处理,然后均进行高温胁迫促进抽薹,采用石蜡切片观察茎尖花芽分化进程,并结合后期抽薹开花情况来判断是否进行春化,并确定其春化类型.结果表明:两个品种在前期经过3种温度处理后,在高温胁迫第8天时均有不同程度的抽薹.两个品种不同温度处理下花芽均进行了分化,前期4 ℃处理并没有使其花芽分化明显提前,后期的高温胁迫可以明显促进花芽分化进程.两品种间在不同温度处理下完成各发育阶段所需天数存在差异,两品种各处理从催芽到开花以及从高温到开花的有效积温也存在差异.前期未经低温处理的叶用莴苣也进入花芽分化、抽薹、现蕾及开花阶段,表明叶用莴苣为非低温春化型植物,后期高温处理能明显促进其抽薹开花,而且从催芽开始只有有效积温达到约2500 ℃·d才能开花.     

春化温度对大白菜花芽分化和抽薹的影响

以冬性有明显差异的6个大白菜品种为试材,研究了4个存化温度对大白菜的花芽分化和抽薹的影响。结果表明,弱冬性材料在3～11℃范围内,花芽分化和抽薹均能在较短的时间完成;强冬性材料适宜的春化温度为3～7℃．超过7℃,花芽分化和抽薹急剧延迟;冬性中等材料适宜的春化温度为3～9℃。故一般采用3～7℃的春化温度对不同冬性材料均适宜。     

低温锻炼后桑树幼苗光合作用和抗氧化酶对冷胁迫的响应

以桑树品种“秋雨”为试验材料,研究了桑树幼苗在低温锻炼、冷胁迫和常温恢复期间的光合作用和抗氧化酶活性的变化.结果表明: 12 ℃3 d低温锻炼明显提高了桑树幼苗的抗冷性.3 ℃3 d冷胁迫下,12 ℃3 d低温锻炼后的桑树幼苗叶片净光合速率(P_n)、气孔导度(G_s)和PSⅡ 最大光化学效率(F_v/F_m)明显高于对照(未经低温锻炼)处理的桑树幼苗,而且其在常温下的恢复也较对照桑树幼苗迅速.在12 ℃ 3 d低温锻炼和3 ℃ 3 d冷胁迫期间,桑树幼苗叶片脯氨酸和可溶性糖含量明显增加,而经低温锻炼的桑树幼苗叶片丙二醛(MDA)含量明显低于未经低温锻炼的桑树幼苗,经低温锻炼的桑树幼苗叶片抗坏血酸过氧化物酶(APX)活性则明显高于未经低温锻炼的桑树幼苗.说明渗透调节物质含量增加和APX活性提高在低温锻炼诱导桑树幼苗的抗冷性上发挥着重要的作用.     

外源一氧化氮对香蕉幼苗抗冷性的影响

以巴西香蕉(Musa AAA Group Cavendish cv.Brazil)幼苗为试验材料,采用外源一氧化氮(NO)供体硝普钠(SNP)15 μmol·L-1溶液进行冷胁迫(8℃)前处理,考察其冷胁迫和常温恢复过程中抗冷性指标的变化,以探讨外源NO对香蕉幼苗抗冷性的影响.结果表明,在8℃冷胁迫环境下,SNP预处理香蕉幼苗的萎蔫程度较轻,且在常温下恢复快而完全.SNP预处理可以显著降低冷胁迫下香蕉幼苗叶片的质膜相对透性及过氧化氢和丙二醛含量,并显著增加其可溶性蛋白含量.在冷胁迫的前2 d,SNP处理苗的过氧化物酶和抗坏血酸过氧化物酶的活性显著增加,而超氧化物歧化酶和过氧化氢酶的活性则在胁迫的第3天才显著上升,经3 d冷胁迫回温(28℃)后,4种酶的活性均显著提高.可见,适当浓度NO能够通过诱导香蕉幼苗体内的抗氧化酶活性来有效缓解其遭受的冷胁迫损伤.     

光周期和温度对草地螟滞育诱导的影响

草地螟Loxostege sticticalis以老熟幼虫滞育越冬。在室内通过人工诱导的方法对其滞育的光周期和温度诱导条件进行了研究。结果表明:草地螟是一种典型的长日照发育型种类。光周期、温度及其交互作用均对草地螟滞育诱导具有重要影响, 其中光周期起主导作用, 温度伴随着光周期起作用。对幼虫滞育诱导最有效的光周期是L12∶D12; 随着温度的升高, 临界光周期呈缩短趋势（18℃除外）。18, 22, 26和30℃条件下幼虫滞育的临界日长依次为13.97, 14.48, 13.92 和12.88 h。光敏感实验揭示:21℃时草地螟对光照反应最敏感时期为幼虫孵化后的11～17 d（约5龄幼虫）, 但孵化后7～11 d（约4龄幼虫）的短光照积累对提高滞育率也有重要作用, 可以将滞育率从40.0%提高到90.0%。     

冷胁迫诱导、咖啡因抑制的水稻根新基因片段的分离及表达分析

利用差异显示（Differential display）及H.Y-Yellow琼脂糖凝胶分离等方法,从冷胁迫和甘露醇共同处理的冷敏感水稻（Wase toitsu）根的总RNA中,分离出冷胁迫诱导的cDNA片段,经过测序和同源比较,发现它是一尚未报道的新基因片段。这一基因的表达对温度具有敏感的反应特性,4℃时表达水平明显增加,在正常温度（25℃）下,其表达水平又可快速降低。当幼苗根用0.5mol/L甘露醇预处理2h后,转入冷胁迫,其低温诱导的表达水平增加更为明显。在甘露醇预处理之前加入咖啡因处理根1h,其表达水平明显降低,几乎与正常温度下的对照相同。据此推测,这一基因可能参与了冷胁迫或水分胁迫诱导的耐冷过程中咖啡因敏感信号的传导。      

变温和恒温对沙葱萤叶甲发育速率的影响

沙葱萤叶甲为近年来在内蒙古草原猖獗成灾的新害虫,为明确温度对其发育速率的影响,分别设置5个变温组合(8/20℃,11/23℃,14/26℃,17/29℃和20/32℃)和6个恒温(13℃,17℃,21℃,25℃,29℃和33℃),比较了变温和恒温对沙葱萤叶甲幼虫和蛹发育速率的影响。结果表明,不同变温组合和恒温对沙葱萤叶甲幼虫和蛹的发育速率有显著的影响。发育历期随温度的升高而缩短,在变温条件下,1龄幼虫期、2龄幼虫期、3龄幼虫期、总幼虫期和蛹期分别从最低温度组合(8/20℃,平均15℃)的11.00,13.44,23.18,46.42和16.89 d,缩短至最高温度组合(20/32℃,平均27℃)的4.92,4.63,9.17,17.83和5.83 d;在恒温条件下,13℃下幼虫不能发育和存活,1龄幼虫期、2龄幼虫期、3龄幼虫期、总幼虫期和蛹期分别从17℃的14.50,10.75,20.63,45.50和11.00 d,缩短至33℃的6.10,5.47,10.60,22.17和5.33 d。在变温条件下,幼虫和蛹的发育起点温度分别为7.44℃和8.48℃,有效积温分别为344.82日度和113.52日度;在恒温条件下,幼虫和蛹的发育起点温度分别为0.64℃和5.11℃,有效积温分别为714.28日度和147.06日度。变温促进了沙葱萤叶甲幼虫和蛹的发育,本研究结果为沙葱萤叶甲的预测预报及综合防控提供了科学依据。     

低温弱光对辣椒幼苗光合特性与光合作用启动时间的影响

以辣椒(Capsicum annuumL.)幼苗为试材,研究了偏低温弱光(19℃/12℃昼/夜,90μmol?m-2?s-1)和临界低温弱光(15℃/8℃昼/夜,90μmol?m-2?s-1)胁迫10 d后的光合特性与光合作用启动时间的变化.结果表明:无论是在偏低温弱光还是在临界低温弱光下,辣椒幼苗的光补偿点(LCP)、光饱和点(LSP)、光饱和时的光合速率(Amax)和表观量子产额(AOY)下降;CO2补偿点(CCP)升高,而CO2饱和点(CSP)、CO2饱和时的光合速率(Amax)以及羧化效率(CE)下降;温度补偿点(TCP)降低;光合作用启动时间(STP)延长.在偏低温弱光下,辣椒幼苗有着更高的光与CO2利用能力和利用效率,光合作用启动时间较短,但温度补偿点较高.     

草地螟阿格姬蜂的滞育诱导和滞育茧的低温贮藏

为了阐明环境因子对草地螟阿格姬蜂Agrypon flexorium (Thunberg)滞育诱导作用, 测定了5个光周期和4个温度处理对阿格姬蜂的滞育诱导和该蜂感受光周期的敏感虫态以及不同时间段低温贮藏对滞育虫茧的影响。结果表明： 在17~23℃、 光照时间10~14 h范围内, 随着温度的降低和光照时间的缩短, 滞育率明显提高。高温能抵消短光照对滞育诱导的影响, 在26℃下, 短光照不能诱导滞育。因此, 低温和短光照是诱导草地螟阿格姬蜂滞育的主要因子。草地螟阿格姬蜂感受滞育信号的敏感虫态为卵和1龄幼虫。卵和1龄幼虫感受滞育信号以后, 需要在滞育环境中发育到老熟幼虫才能全部进入滞育。将室内诱导的滞育茧在4℃左右环境条件下冷藏80 d, 成蜂的羽化率和寄生能力与没有冷藏的非滞育茧差异不显著, 冷藏120 d, 滞育茧仍有71.7%可以正常羽化。结果说明,可在17℃,光周期8L∶16D条件下对寄生后3 d内的草地螟Loxostege sticticalis幼虫进行滞育诱导, 滞育后的虫茧最佳贮藏时间为80 d, 不宜超过120 d。本研究为室内扩繁、 防止蜂源退化、 控制寄生蜂发育时间以便适时释放提供了参考依据。     

六种藓类植物茎的比较解剖学研究

通过对6种藓类植物,即褶叶青藓(Brachythecium salebrosum(Web.et Mohr.)B.S.G.)、湿地匐灯藓(Plagiomnium acutum(Lindb.)Kop.)、侧枝匐灯藓(Plagiomnium maximoviczii(Lindb.)Kop.)、大凤尾藓(Fissidensnobilis Griff.)、大羽藓(Thuidium cymbifolium(Doz.et Molk.)B.S.G.)和大灰藓(Hypnum plumaeforme Wils.)嫩茎和老茎的石蜡切片和显微观察发现,同一藓类植株的嫩茎和老茎,茎结构稳定,不同种藓类植物茎横切面具有不同特征.植物体茎横切面形状、表层细胞的层数、细胞大小和细胞壁厚薄、皮层细胞大小和形状、中轴的有无以及比例等特征可以作为藓类植物的分科分类依据之一.     

Cause of Senescence of Nine Sorts of Flowers

The levels of endogenous phytohormones and respiratory rate in nine sorts of flowers such as Cymbidium faberi Rolfe, Nopalxochia ackermannii Kunth and others were investigated both at full bloom and senescence and meanwhile the effect of exogenous phytohormones on prolonging the blossoms and promoting ethylene production were tested. There is a high content of endogenous ethylene in all the long-lived flowere, about 3–16 folds higer than the short-lived ones. There is a high level of ABA at full blooming flowers of short-lived flowers, in which there is no or only some cytokinins in it, but the ratio of CTK (6BA+zeatin)/ABA is smaller(l.7). The endogenous ABA reached a much higher level at senescence in all nine sorts of flowers, so it is reasonable to consider that it is ABA which plays an important role of regulation in controlling flower's senescence. There is a much higher level of GA3 and zeatin in the long-lived flowers which is not demonstrated in the shortlived ones. The respiratory rate is one of the factors controtling the longevity of flowers, but it does not play a decided role. Application of 6BA and zeatin prolongs distinctly orchid’s longevity, however exogenous IAA through the promotive action on ethylene production, evidently extends the longevity of the flowers of the Nopalxochia ackermannii Kunth.     

Photoregulation of seed germination of wild-type and of an aurea-mutant of tomato

Seed germination of an aurea mutant of tomato ( Lycopersicon esculentum Mill.) is promoted by continuous irradiation with red, far-red or long-wavelength far-red (758 nm) light as well as by cyclic irradiations (5 min red or 5 min far-red/25 min darkness). Far-red light applied immediately after each red does not change the germination behaviour. Seed germination of the isogenic wild-type, cv. UC-105, is promoted by continuous and cyclic red light while it is inhibited by continuous and cyclic far-red light and by continious 758 nm irradiation. Far-red irradiation reverses almost completely the promoting effect of red light. The promoting effect (in the aurea mutant) and the inhibitory effect (in the wild-type) of continuous far-red light do not show photon fluence rate dependency above 20 nmol m⁻² s⁻¹. It is concluded that phytochrome controls tomato seed germination throgh low energy responses in both the wild type and the au mutant. The promoting effect of continuous and cyclic far-red light in the au mutant can be attributed to a greater sensitivity to P_fr.     

真菌类遗传学分析的知识结构教学

本文以认知结构理论为指导,讨论了真菌类遗传分析与高等动植物遗传分析的内在联系,认为利用这种内在联系进行教学可收到好的效果并说明了作者的具体教学过程。 Abstract:In the paper, the relationship between genetic analysis of Fungi and genetic analysis of high animal and plant was discussed.A good results were obtained when we adopted this method in the teaching.     

龙胆科药用植物化学成分的研究现状

龙胆科植物在我国的分布范围很广,且多数为药用植物,其多数种属的药用植物,至今其化学成分尚未被系统研究。综述了目前龙胆科药用植物的化学成分的研究现状及一般提取方法,对近年来发现的环烯醚萜及裂环烯醚萜类化合物进行了总结,为本科药用植物的更深入研究提供了参考。     

The effects of glutamine of the maintenance of embryogenic cultures of Cryptomeria japonica

Summary Embryogenic tissues of sugi (Cryptomeria japonica) were induced on a modified Campbell and Durzan (CD) medium containing 1 μM 2,4-dichlorophenoxyacetic acid (2,4-D) and 600 mg l⁻¹ glutamine, and subcultured in the medium of the same composition for over 1 yr. This resulted in a mixed culture of embryogenic and non-embryogenic cells. When embryogenic cells were isolated and cultured independently, their capacity to form embryogenic aggregates was lost. Thus, the non-embryogenic cells present within a mixed culture system were essential to the formation of embryogenic aggregates. When embryogenic tissues were isolated and cultured independently on a high glutamine-containing (2400 mg l⁻¹) medium, dry weights and endogenous levels of glutamine increased, and the tissue could generate a large number of embryogenic aggregates. Amino acid analysis of embryogenic and non-embryogenic cells from the maintenance culture indicated a higher level of glutamine was present in the latter. The high endogenous level of glutamine in the non-embryogenic portion of mixed cell masses may be the supplier of glutamine for maintaining the embryogenic property of the tissues.     

Specificity of action of piperidylcholine derivatives as substrates of cholinesterases of various origin

The review deals with study of enzymologic properties of a novel highly specific acetylcholinesterase substrate, N-(β-acetoxyethyl) piperidinium iodomethylate (“piperidylcholine”), and its 30 derivatives that were tested as effectors of cholinesterases of mammals and various species of Pacific squids. It was proven for the first time that responsible for specificity of action was structure of cyclic ammonium grouping of the alcohol part of molecule of the ester substrate. Analysis of specificity is performed based on enzymatic hydrolysis parameters—activity of catalytic center of cholinesterases and bimolecular constant of the reaction rate that are determined at optimal and low substrate concentrations. Among the specially synthesized group of thioester compounds there is revealed one more highly specific acetylcholinesterase substrate—N-(β-acetoxyethyl) piperidinium.     

Interconnection of parameters of regulation system of lipid peroxidation and of morphophysiological parameters of mouse liver

A complex analysis of seasonal fluctuations of the mean group parameters of the system of regulation of lipid peroxidation has been performed in liver of Balb/c mice. Association of lipid characteristics and morphophysiological parameters is studied in the Balb/c mouse liver. An inter-connection is revealed between the liver index and the amount of lysoforms of phospholipids, the scale and character of the interconnection differing essentially depending on proportion of phos-phatidylcholine in mouse liver phospholipids.