麦后移栽棉生育及生理特性对水分亏缺的响应

在防雨棚测坑试验条件下,研究了不同生育阶段水分亏缺对麦后移栽棉生长发育及生理特性的影响。结果表明,蕾期水分亏缺抑制了植株的正常生长发育,棉花株高、茎粗和叶面积指数等生长发育指标均随水分亏缺程度的增大而减小,而花铃期水分亏缺对其影响较小;在植株快速生长阶段,蕾铃数和叶面积指数呈现良好的对数正相关关系,决定系数达到0.90以上;不论蕾期还是花铃期,与对照处理相比,水分亏缺均显著提高了叶片可溶性糖和丙二醛(MDA)的质量分数,且随水分亏缺程度的增大而增大,进而限制了蕾铃的正常生长发育,复水后可溶性糖与MDA均降低至与对照无明显差异的程度。     

Stimulation of ROS-scavenging systems in squash (Cucurbita pepo L.) plants by compost supplementation under normal and low temperature conditions

The beneficial effect of compost, the final product of aerobic biodegradation of organic matter, on growth, lipid peroxidation [as malondialdehyde (MDA], hydrogen peroxide (H₂O₂) and superoxide anion (O₂^•−), activities of superoxide dismutase (SOD), catalase (CAT), ascorbate peroxidase (APX) and glutathione reductase (GR), as well as reduced ascorbate (ASC) and glutathione (GSH) and their oxidized forms was investigated in squash (Cucurbita pepo L. cv. Eskandarany) plants exposed to normal and low temperature (LT) conditions. LT stress of 8 °C significantly reduced the plant growth of untreated plants, but compost alleviated the adverse effect of stress and significantly increased the fresh and dry weights under normal and stress conditions. LT also induced accumulation of H₂O₂ and O₂^•− and resulted in increased lipid peroxidation, pointing out to cellular oxidative stress. Under compost application, such reactive oxygen species (ROS) and peroxidized lipids were markedly reduced, but SOD, CAT, APX and GR activities, key enzymes of ROS-scavenging systems, were significantly increased. Data also indicated that there were general reductions in total ascorbate and glutathione pool in LT control plants, but compost-treated ones considerably have maintained higher levels of such redox metabolites. Significantly higher ratios of ASC/DHA (dehydroascorbate) and GSH/GSSG (glutathione disulfide) were generally found in compost-treated plants than in untreated-ones. It is evident that compost induced enhancement of LT tolerance was related to up-regulation of enzymatic and non-enzymatic antioxidant systems. Such enhancement would eventually protect plant cells from LT-induced oxidative stress reactions via scavenging ROS.     

与水稻耐逆性相关的叶片丙二醛含量的QTL分析

丙二醛（MDA)是膜脂过氧化的终产物,其含量可用来反映植物对逆境条件的反应强弱。利用由247个株系组成的珍汕97B/密阳46重组自交系（RIL）群体及其分子标记连锁图谱,检测了控制水稻丙二醛（MDA）含量的数量性状基因座位（QTL）。所测性状在RIL群体中出现超亲分离。在第1染色体的RG532-RG811和RG381-RG236标记区间,共检测到2个控制水稻叶片MDA含量的QTL,加性效应分别来自母本珍汕97B和父本密阳46,贡献率分别为4.33%和462%。     

BDE3胁迫对翡翠贻贝（Perna viridis）SOD、MDA和GSH的影响

采用半静态试验方法,研究不同质量浓度的一溴联苯醚（BDE3）（1 μg·L-1、10 μg·L-1和100 μg·L-1）胁迫1 d、3 d、7d和15 d且清洁海水释放3 d和7 d后,翡翠贻贝（Perna viridis）外套膜和内脏团超氧化物歧化酶（SOD）活性、丙二醛（MDA）质量摩尔浓度和谷胱甘肽（GSH）质量分数的变化规律。结果表明,BDE3胁迫后低浓度组翡翠贻贝两组织SOD活性均受到诱导（P〈0.01）,诱导率随胁迫时间延长而下降,中、高浓度组外套膜对BDE3响应比内脏团灵敏;BDE3对翡翠贻贝外套膜b（MDA）的影响总体呈诱导后抑制趋势,对内脏团b（MDA）的影响表现抑制-诱导反复变化,其中低浓度组第3天时诱导率最高（26.04%）,高浓度组第7天时抑制率最高（14.92%）;翡翠贻贝外套膜w（GSH）在（BDE3）迫下,低浓度组一直被诱导（P〈0.01）,中、高浓度组总体呈诱导后抑制作用,内脏团中高浓度组w（GSH）胁迫第1天受到显著抑制（P〈0.05）,随暴露时间的延长,低浓度组w（GSH）显著增加（P〈0.01）,中、高浓度组出现诱导抑制的不规律变化。释放阶段结束后仅个别浓度组恢复至对照组水平。     

茶多酚对高酒糟日粮肉鸡生产性能和抗氧化特性的影响

本研究旨在评估添加茶多酚对高酒糟(distillers dried grain with solubles DDGS)日粮肉鸡生产性能和抗氧化特性的影响。将400只21日龄肉鸡随机分为5个处理,每个处理4个重复,每个重复20只。正对照组为玉米-豆粕型日粮,负对照组为玉米-豆粕-DDGS型日粮(15%DDGS),处理组分别在负对照日粮中添加100、300、500 mg/kg茶多酚。结果表明,与正对照组相比,后期日粮中添加15%DDGS对肉鸡生产性能无显著影响(P>0.05),但血液的GSH-Px降低8.31%(P<0.01),胸腿肉T-AOC含量降低,腿肉MDA值显著升高(P<0.05)。添加茶多酚提高了血液的T-AOC和GSH-Px活性(P<0.05)。随着茶多酚添加剂量的升高,T-AOC和GSH-Px有升高的趋势,但各水平组之间差异不显著;茶多酚添加300 mg/kg以上能显著降低胸腿肌MDA值(P<0.05),提高T-AOC含量,改善肉质的抗氧化特性。本研究结果表明,在肉鸡高DDGS日粮中添加茶多酚可以改善肉鸡机体及肉质的抗氧化特性。     

BHT对苹果采后灰霉病的防效及防御酶活性和丙二醛含量的影响

为探究2,6-二叔丁基-4-甲基苯酚(2,6-di-tert-butyl-4-methylphenol,BHT)对苹果采后灰霉病的防效和防病机制,采用平板法和刺伤接种法测定了BHT对灰霉病菌Botrytis cinerea的抑制作用及果实内防御酶活性和丙二醛含量的影响。结果表明,0.1 mmol/L BHT对苹果灰霉病的防效最佳,处理苹果后间隔48～96 h接种灰霉病菌,其防效可达68.59%～73.55%,其次为0.2、1.0 mmol/L BHT处理,但防效均低于52.94%。0.1 mmol/L BHT处理对灰霉病菌菌丝生长和分生孢子萌发无显著抑制作用,但可显著增强果实内超氧化物歧化酶、过氧化物酶和过氧化氢酶的活性以及总抗氧化能力,其峰值是对照的1.82～5.28倍,且均显著高于单独接种灰霉病菌的处理。此外,单独接种灰霉病菌的苹果果实内丙二醛含量快速升高,最大增幅达251.49%,而BHT处理后丙二醛含量变幅较小,最大增幅仅为83.95%。表明BHT可通过增强苹果果实内防御酶活性水平和总抗氧化能力来降低丙二醛的积累,从而提高果实对灰霉病的抗性。     

高温胁迫对棘胸蛙蝌蚪抗氧化酶活力的影响

实验利用水温从18~30℃骤升和缓升两种模式,高温胁迫处理棘胸蛙(Quasipaa spinosa)蝌蚪后,提取其尾部肌肉和内脏团的组织液,进行乳酸脱氢酶(LDH)、谷胱甘肽过氧化物酶(GSH-Px)、超氧化物歧化酶(SOD)、过氧化氢酶(CAT)、碱性磷酸酶(AKP)等酶活力和丙二醛(MDA)含量测定。结果表明,棘胸蛙蝌蚪尾部肌肉提取液的LDH活力显著高于内脏团(P0.01);高温胁迫下棘胸蛙蝌蚪尾部肌肉和内脏团提取液的LDH活力显著提高(P0.01)。高温胁迫下棘胸蛙蝌蚪尾部肌肉和内脏团的GSH-Px活力均显著降低(P0.01,P0.05),且水温骤升模式下的内脏团GSH-Px活力显著高于缓升模式(P0.01)。在30℃高温胁迫时,棘胸蛙蝌蚪尾部肌肉和内脏团SOD活力均显著降低(P0.05,P0.01),且水温骤升模式的棘胸蛙蝌蚪尾部肌肉和内脏团SOD活力均高于缓升模式(P0.05,P0.01)。高温胁迫下CAT活力均显著下降(P0.01),且缓升模式下的棘胸蛙蝌蚪CAT活力显著高于骤升模式(P0.05,P0.01)。在两种升温模式下,高温胁迫对尾部肌肉的AKP活力均无显著影响;而在骤升模式下,高温胁迫的棘胸蛙蝌蚪内脏团的AKP活力显著提高(P0.05)。高温胁迫下的棘胸蛙蝌蚪尾部肌肉和内脏团MDA含量均显著升高(P0.01),骤升模式下高温胁迫的棘胸蛙蝌蚪内脏团的MDA含量显著高于尾部肌肉(P0.01)。     

广西花生品种（系）苗期生长耐旱性及相关生理特性研究

花生苗期生长受干旱影响最大,且干旱是广西花生生产上重要的限制因素。选择广西主推及新育成的花生品种（系）共11个,在人工防雨棚下进行土培盆栽试验,以正常淋水（2d供水1次）为对照,以人工控水（10d供水1次）作为干旱胁迫处理,反复干旱胁迫30d时,测定花生苗期的主茎高尧侧枝长、生物量以及叶绿素、可溶性糖、丙二醛尧脯氨酸含量,计算花生苗期生长生理受抑制程度及生长耐旱隶属函数值。结果表明,在干旱胁迫下,各参试花生品种的主茎高、侧枝长和生物量均受到不同程度的抑制,其中桂花819的生长受抑制程度最轻。从各参试品种苗期耐旱隶属函数值排名可知,桂花819的苗期生长耐旱性最强,其次是桂花红166、桂花21和桂花26;大多数品种的叶绿素、可溶性糖、丙二醛尧脯氨酸含量在干旱胁迫下增加,少数花生品种表现出降低趋势,且苗期耐旱品种桂花819的叶绿素和脯氨酸含量比对照的增加量最大,丙二醛和可溶性糖含量增加量也较大。     

Changes in antioxidative system and membrane damage of lettuce in response to salinity and boron toxicity

Individual and combined effects of salinity and B toxicity on growth, the major antioxidant enzymes (superoxide dismutase, SOD; catalase, CAT; ascorbate peroxidase, APX) activities, ascorbic acid, proline, and H₂O₂ accumulation, and stomatal resistance (SR), malondialdehyde (MDA), membrane permeability (MP) and the concentrations of sodium (Na), chloride (Cl) and boron (B) of lettuce were investigated. Boron toxicity and salinity reduced growth of lettuce plants. Under B toxicity, B concentration of the plants was increased, but in the presence of NaCl, the concentration of B was significantly reduced. Sodium and Cl concentrations were increased in B + NaCl and NaCl treatments. Membrane damage was more pronounced in NaCl and B + NaCl treatments. Stomatal resistance of the plants was significantly increased by salinity treatments. The accumulation of proline and ascorbic acid was the highest in the B + NaCl treatment. In general, stress conditions significantly increased H₂O₂ and antioxidant enzyme (SOD, CAT and APX) activities. The present results indicate that stomatal closure is an important response of lettuce against NaCl and B + NaCl stress. Furthermore NaCl and B + NaCl toxicity-induced oxidative stress in lettuce resulting in lipid peroxidation and membrane damage. Increased antioxidant enzyme activities and also accumulation of ascorbic acid and proline are involved in order to overcome B- and NaCl-induced oxidative stress.     

Antioxidant role of propolis extract against oxidative damage of testicular tissue induced by insecticide chlorpyrifos in rats

Pesticides induce oxidative stress leading to generate free radicals and alternate the antioxidant or oxygen free radical scavenging enzyme system. This study was conducted to investigate the oral toxicity of chlorpyrifos toward male rat and the oxidative stress of the sub-lethal dose (9 mg/kg; 1/25 LD₅₀) on the lipid peroxidation level (LPO), reduced glutathione content (GSH) and antioxidant enzymes; catalase (CAT), superoxide dismutase (SOD), glutathione peroxidase (GPx) and glutathione-S-transferase (GST) activities of testicular tissue. Also, the protective effects of propolis extract (50 mg/kg b.w.) alone or in combination with chlorpyrifos were investigated. The oral administration of chlorpyrifos significantly caused elevation in LPO level by 1.79-fold as compared to control. The activities of antioxidant enzymes including CAT, SOD, GPx and GST were decreased significantly (23.66%, 27.75%, 29.13% and 11.52%) as well as the level of GSH decreased by 21.97% in testicular tissue as compared to control animals. Co-administration of propolis extract with chlorpyrifos or alone in male rats decreased LPO level, normalized CAT, SOD GPx and GST activities, while GSH content was increased in testicular tissue. We conclude that propolis extract significantly reduces chlorpyrifos-induced oxidative stress in rat testis and the protective effect of the pre-treatment with propolis extract as attenuating agent could be due to its antioxidant properties.