S3307浸种对黄瓜幼苗生理的影响

用S3307粉剂不同浓度对“夏丰一号”黄瓜浸种,研究S3307对幼苗生长的生理效应,目的是得到培育黄瓜壮苗适宜的处理浓度。结果表明：与对照相比,经10,20,50μg/L的S3307浸种后,均不同程度地增加了黄瓜幼苗叶片中叶绿素和可溶性糖含量,提高了叶片光合速率和SOD活性,降低了MDA含量,其中,以２０μｇ／Ｌ浸种处理16h的效果最佳。     

镧浸种对盐胁迫下小麦幼苗生长及其生理特征的影响

通过水培方式研究了0、25、50和100 mg/L硝酸镧浸种对盐胁迫条件下小麦品种临抗11和临优2069根系及幼苗生长的影响.结果表明:(1)与对照组相比,盐胁迫处理小麦幼苗植株矮,根系短,叶片叶绿素含量、根系活性吸收面积以及SOD和CAT活性明显降低,叶片MDA与Pro含量水平显著上升;在钠离子浓度相同的情况下,Na2CO3对小麦生长的影响大于NaCl.(2)适当浓度硝酸镧浸种处理增加了盐胁迫下小麦幼苗的株高、总根长、根系活性吸收面积及SOD和CAT活性,且各指标在盐胁迫下增加幅度高于正常水分处理.(3)2个小麦品种对镧处理的敏感程度存在差异,不同小麦品种及不同盐胁迫下最适的镧浸种浓度不同.研究发现,适当浓度镧浸种能有效缓解盐胁迫对小麦幼苗的伤害,具有显著促进小麦根系生长、培育壮苗的作用.     

S3307浸种对番茄幼苗生长和一些生理指标的影响

以不同浓度S3307浸种后,番茄幼苗株高降低,茎粗度增加,根冠比值、叶绿素、光合速率、可溶性糖、脯氨酸、Vc含量、超氧化物歧化酶(SOD)和过氧化物酶(POD)活性均提高,丙二醛(MDA)含量和外渗电导率降低。说明S3307有助于培育壮苗,并提高番茄幼苗的抗逆性。5mg·L~(-1) S3307浸种的效果明显。     

硅提高黄瓜幼苗抗盐能力的生理机制研究

为了明确硅提高黄瓜幼苗抗盐能力的机制,该试验采用水培方法,以黄瓜品种‘津优一号’为材料,对幼苗进行中度盐胁迫,研究在盐胁迫下硅对黄瓜幼苗生长、光合特性、渗透调节物质和离子吸收的影响。结果显示:(1)正常条件下,硅对黄瓜幼苗生长及相关生理指标无明显影响;单独盐处理降低了幼苗叶片叶绿素含量、光合速率、气孔导度、蒸腾速率和叶片含水量,导致幼苗生长受抑。(2)盐胁迫下加硅显著提高了幼苗光合速率和叶片含水量,增加了生物量的积累;在盐胁迫初期,硅加盐处理黄瓜叶片渗透势略低于单独盐处理,此后均高于单独盐处理;硅加盐处理显著提高了叶片可溶性糖含量,尤其是蔗糖含量,而降低了其脯氨酸含量,但对可溶性蛋白含量无显著影响。(3)盐胁迫下黄瓜植株Na+含量大幅上升,K+含量下降,K+/Na+比大幅降低;硅加盐处理降低了黄瓜叶片中Na+含量,提高了K+含量和K+/Na+比。研究表明,盐胁迫条件下,硅能通过减轻叶片离子毒害和增加水分吸收,改善叶片水分状况,从而维持较高的光合能力,提高其抗盐能力;而渗透调节只在盐胁迫初期有轻微缓解作用,不是硅提高黄瓜幼苗抗盐性的主要途径。     

叶面喷施烯效唑对盐胁迫下大豆幼苗生理及解剖结构的影响

以大豆栽培品种‘中黄13’为试验材料,在筛选合适的盐胁迫及烯效唑(S3307)浓度基础上,采用大豆幼苗期盐胁迫以及叶面喷施S3307的方法,分析比较相关生理指标及营养器官(根、茎和叶)解剖结构的差异,从组织结构形态和生理两方面探讨叶面喷施S3307对大豆苗期盐胁迫的缓解效应及其作用机制。结果显示:(1)与正常生长的对照相比,盐胁迫下大豆根和叶中硫代巴比妥酸反应物的含量均显著增加,叶绿素含量显著降低;而且叶片较薄,海绵组织和栅栏组织细胞排列混乱;根部中柱所占比例较对照明显变小,但皮层所占比例变大,外表皮细胞向内凹陷,次生导管平均孔径较小且含有侵填体;茎部解剖结构的变化与根部相类似。(2)叶面喷施80mg/L S3307后,盐胁迫大豆植株根和叶中硫代巴比妥酸反应物和叶绿素含量均恢复到接近对照的水平,且根、茎和叶解剖结构变化介于正常对照与盐胁迫处理之间。研究表明,叶面喷施80mg/L S3307能够有效缓解盐胁迫对大豆的伤害,且这种缓解作用与叶片细胞膜伤害、光合色素含量以及根、茎和叶内部组织结构改变有关,叶面喷施S3307可能是生产上提高大豆耐盐性的一种有效措施。     

多效唑浸种对NaCl胁迫麻疯树幼苗的生长调节效应

以'南油1号'麻风树幼苗为材料,通过盆栽试验研究了200 mmol·L-1 NaCl胁迫处理对不同浓度(0～1 000 mg·L-1)多效唑(PP333)浸种麻疯树幼苗生长和光合作用的影响.结果显示:在盐胁迫下,不同浓度的PP333浸种处理均显著降低麻疯树植株株高,但是均显著提高了盐胁迫下株高相对生长速率,同时提高了其干物质积累速率、根含水量、根冠比、叶绿素含量和净光合速率;并提高了幼苗根、叶的K+含量,降低根、叶的Na+和Cl-含量,从而提高根、叶的K+/Na+比率.研究表明,PP333浸种能缓解盐胁迫下麻疯树幼苗的失水程度和光合色素的下降幅度,有效改善其光合作用效率,同时维持体内的离子平衡,从而减轻盐胁迫伤害,促进植株生长,并以600 mg·L-1 PP333浸种效果最好.     

La（NO3）3浸种对NaCl胁迫下红小豆幼苗生长的影响

采用向1／2Hoagland营养液中按一定比例添加中性盐（NaCl）模拟盐胁迫的方式,研究了h（NO3）,浸种对盐胁迫下红小豆（Phaseolus angularis）幼苗生长的影响。结果表明：（1）与对照组相比,盐胁迫不同程度地降低了红小豆幼苗的株高、叶面积、地上部分鲜重、总根数及根系活力、根苗SOD、POD、CAT活性等,明显增加了根苗MDA含量水平。（2）使用适当浓度的La（NO3）3浸种可以提高对照组和盐处理组红小豆的株高、叶面积、总根长、总根数、叶绿素、根活力及SOD、POD和CAT活性,也可以显著降低根苗MDA含量水平,且大多表现出在盐胁迫下变化幅度高于正常处理。La（NO3）3浸种有利于缓解盐胁迫带来的不良影响。（3）低浓度的La（NO3）3浸种处理能够提高红小豆幼苗的耐盐性,缓解盐胁迫伤害,而高浓度处理则加剧了盐胁迫伤害。30mg／L La（NO3）3浸种对提高红小豆幼苗耐盐性的效果最好。     

腐植酸浸种对盐碱胁迫下小麦幼苗抗氧化系统的影响

对龙麦26和克旱16两种不同基因型春小麦品种进行腐植酸浸种处理,研究了腐植酸对盐(NaCl)、碱(Na CO3)两种胁迫下小麦幼苗抗氧化系统的影响.结果表明:盐碱胁迫下小麦幼苗叶片脯氨酸含量增加,膜透性增强,地上部鲜质量降低;盐胁迫下,过氧化氢酶(CAT)活性升高,过氧化物酶(POD)活性降低,超氧化物歧化酶(SOD)活性先升后降,而碱胁迫下CAT和POD活性均升高,SOD活性降低;碱胁迫处理的小麦幼苗叶片抗氧化酶系统活性高于同浓度的盐胁迫处理;腐植酸浸种提高了小麦叶片谷胱甘肽含量,提高了SOD和CAT活性,有效缓解了盐碱胁迫对幼苗生长的影响.不同基因型小麦品种在抵御盐碱胁迫的能力和机制上存在一定差异,且与盐离子组成、浓度间存在一定互作,并受浸种方式调控.     

La(NO3)3浸种对NaCl胁迫下红小豆幼苗生长的影响

采用向1/2Hoagland营养液中按一定比例添加中性盐(NaCl)模拟盐胁迫的方式,研究了La(NO3)3浸种对盐胁迫下红小豆(Phaseolus angularis)幼苗生长的影响.结果表明:(1)与对照组相比,盐胁迫不同程度地降低了红小豆幼苗的株高、叶面积、地上部分鲜重、总根数及根系活力、根苗SOD、POD、CAT活性等,明显增加了根苗MDA含量水平.(2)使用适当浓度的La(NO3)3浸种可以提高对照组和盐处理组红小豆的株高、叶面积、总根长、总根数、叶绿素、根活力及SOD、POD和CAT活性,也可以显著降低根苗MDA含量水平,且大多表现出在盐胁迫下变化幅度高于正常处理.La(NO3)3浸种有利于缓解盐胁迫带来的不良影响.(3)低浓度的La(NO3)3浸种处理能够提高红小豆幼苗的耐盐性,缓解盐胁迫伤害,而高浓度处理则加剧了盐胁迫伤害.30 mg/L La(NO3)3浸种对提高红小豆幼苗耐盐性的效果最好.     

NaCl胁迫下SA浸种绿豆幼苗的生长及生理特征

以'中绿一号'绿豆品种为材料,对不同浓度水杨酸(SA)浸种绿豆种子在NaCl胁迫条件下的萌发、幼苗生长及相关生理指标变化进行分析.结果显示:(1)与未胁迫对照相比,未浸种对照绿豆在100～500 mmol·L-1 NaCl处理下的发芽率、芽长、根长和叶片叶绿素含量显著降低,而幼苗叶片丙二醛(MDA)与脯氨酸(Pro)含量水平显著上升(P＜0.05),且其升降幅度随NaCl胁迫浓度提高而增加;(2)与未浸种对照相比,未胁迫对照种子的萌发和幼苗的生长在20 mg·L-1 SA处理中受到抑制,而在40～80 mg·L-1 SA处理条件下得到促进,至100 mg·L-1 SA时又受到显著抑制.(3)适当浓度的SA浸种能够显著提高盐胁迫下绿豆幼苗的芽长、根长、叶绿素的含量,降低了MDA和Pro含量;在NaCl胁迫浓度为100～300 mmol·L-1时的SA适宜浓度浸种为60 mg·L-1,而500 mmol·L-1 NaCl时为80 mg·L-1.研究表明,适当浓度的SA浸种能有效缓解盐胁迫对绿豆幼苗的伤害,提高其耐盐性.     

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.