遮荫处理及恢复光照对白菜生长及活性氧代谢的影响

 以白菜耐弱光品种‘矮王’和不耐弱光品种‘绿优’为材料,研究遮荫处理及恢复光照过程中植株生长、活性氧代谢和抗氧化酶活性的变化。结果表明,遮荫处理后‘矮王’品种生长减缓, ‘绿优’品种生长停滞;2品种的MDA含量、O₂-. 产生速率和H₂O₂含量呈现先下降后上升的趋势, POD活性呈上升趋势,而SOD、CAT、APX等酶活呈先下降后上升的趋势;恢复生长光照后,2品种的 MDA含量、O₂-. 产生速率和H₂O₂含量均迅速上升,几种酶活也呈加速上升趋势。遮荫处理后期与恢复光照后‘绿优’的膜脂过氧化现象较‘矮王’严重,‘矮王’通过增加抗氧化酶活性,有效地减轻了膜脂过氧化程度。     

甲氧基丙烯酸酯类杀菌剂在我国的登记用量分析

为探究嘧菌酯与硒代蛋氨酸复合暴露后对水体生物早期发育的影响,采用半静态试验法,测定了等毒性配比的嘧菌酯和硒代蛋氨酸二元混合体系复合暴露对水生模式生物斑马鱼胚胎及仔鱼的发育毒性及对相关酶活性的影响。结果表明：经不同质量浓度的嘧菌酯和硒代蛋氨酸(0.1 + 0.2、0.25 + 0.5、0.5 + 1.0和1.0 + 2.0 mg/L) (其中硒代蛋氨酸按硒元素的质量计,下同)复合暴露后,胚胎出现自主运动次数减少、孵化率降低、死亡率增加及心率下降现象,同时仔鱼体长受到显著抑制,且呈现明显的时间-剂量-效应关系;与对照组相比,在嘧菌酯和硒代蛋氨酸不同质量浓度(0.0005 + 0.001、0.005 + 0.01和0.05 + 0.1 mg/L)复合暴露下,斑马鱼仔鱼体内过氧化氢酶(CAT)活性显著降低,且高浓度复合暴露组(0.05 + 0.1 mg/L)的抑制作用最显著(P < 0.01),而对超氧化物歧化酶(SOD)活性则无显著影响;与对照组相比,高浓度复合暴露组显著抑制了线粒体呼吸链复合体Ⅲ的活性(P < 0.05),而其余浓度复合暴露组差异不显著。研究结果表明,经嘧菌酯与硒代蛋氨酸不同质量浓度复合暴露(0.1 + 0.2、0.25 + 0.5、0.5 + 1.0和1.0 + 2.0 mg/L)后,会对斑马鱼胚胎及仔鱼发育产生毒性效应,但在目前自然水体环境实际浓度水平下,除了抑制CAT活性外,尚不会产生其他毒性效应。以上研究结果可以为水体环境中嘧菌酯和硒代蛋氨酸浓度监测及复合暴露的生态风险评估提供数据支撑。     

Effects of xylanase supplementation on growth performance,nutrient digestibility,blood parameters,fecal microbiota,fecal score and fecal noxious gas emission of weaning pigs fed corn‐soybean meal‐based diet

This study was conducted to evaluate the effects of xylanase supplementation on nutrient digestibility, growth performance, blood parameters, fecal microflora shedding, fecal score and fecal noxious gas emission of weaning pigs fed corn‐soybean meal based diet. A total of 150 weaning pigs with an average initial body weight (BW) of 7.85 ± 0.93 kg were randomly allocated to three treatments based on BW and sex (10 replicate pens with five pigs, two gilts and three barrows) were used in this 42‐day trial. Dietary treatments were: (1) CON, basal diet; (2) X1, basal diet +0.005% xylanase; (2) X2, basal diet +0.01% xylanase. The xylanase supplementation linearly increased (P < 0.05) average daily gain (ADG), and gain : feed ratio (G:F) from days 29 to 42 and the in overall period, dry matter, nitrogen and energy digestibility, and fecal Lactobacilli counts, and linearly decreased (P < 0.05) blood urea nitrogen (BUN) concentration, fecal NH₃ and H₂S emission. Additionally, at weeks 5 and 6, there was a linear decrease in fecal score with xylanase supplementation. In conclusion, dietary supplementation of xylanase improved growth performance, nutrient digestibility, shifted microbiota by increasing fecal Lactobacillus counts, decreased BUN concentration, fecal score, and fecal NH₃ and H₂S emission in weaning pigs.     

杨桃果实生长发育过程中营养品质的变化

杨桃（Averrhoa arambola L．）为华南地区重要的热带水果。本试材为华南农业大学园艺分场种植的3年生盆栽马来西亚甜杨桃，砧木为酸杨桃。在杨桃的开花期，选择生长势、开花数量和时间较一致45株为试材，再选择受精时间一致的果实做标记。采样时问从开花后（2003年7月15日）至杨桃充分成熟（2003年10月25）。测定杨桃果实中的糖（蒽酮比色法）、有机酸（HPLC法）、维生素C（2，6-二氯靛酚钠滴定法）和单宁（高锰酸钾滴定法）的含量。     

不同向日葵品种对黄萎病的抗性*

采用浸根接种法鉴定不同向日葵种质资源对黄萎病的抗性差异。结果表明：40份供试向日葵品种依据抗性划分标准共分为3类,其中中抗品种有5份如：‘118’、‘新葵杂5号’等;低抗品种有8份如‘767’、‘KJ003’等;其余27份供试材料均呈现感病;没有鉴定出免疫和高抗的向日葵品种。     

抗旱保水袋性能及其在容器苗中的试验研究

为探讨抗旱保水袋在废弃采石场造林中的应用效果,通过室内试验和室外盆栽试验研究了抗旱保水袋性能及对容器苗生长的影响。结果表明:大袋保水袋的吸水速率和吸水倍数比小袋保水袋分别增加1.4倍、1.9倍,在蒸馏水溶液下的吸水速率和吸水倍数比自来水分别增加0.6倍、0.1倍;大袋保水袋的保水率大于小袋保水袋;保水袋能显著增加渣土土壤体积含水量,比对照高1.29倍,苗高平均比对照增加2.36cm,成活率平均比对照增加69.5%,出现死亡天数平均比对照推迟12d。结论得出,抗旱保水袋是干旱、半干旱及半湿润地区废弃采石场困难立地提高造林成活率并促进植被恢复的一种有效方法。     

湖北省福寿螺分布调查

对湖北省福寿螺(Pomacea canaliculata)分布地区进行了调查,并确认福寿螺在湖北省的北缘分布地区为宜昌市夷陵区黄柏河—远安县洋坪镇(凤凰村)—荆州市沙市区八岭山镇(童桥村)—潜江市渔洋镇(排湾村)—孝感市孝南区三汊河镇(龙岗村)—武汉市黄陂区前川街(下石村)—英山县红山镇(东汤河村)一线,纬度30°~31°,其中最北端分布地区为远安县洋坪镇,东经111°34′57.97″,北纬31°11′3.36″。湖北省福寿螺分布地区的立地条件均同时具备一定深度水体(深10 cm以上)和一定深度的淤泥(深10 cm以上),且可能覆盖度较高的水生植被更有利于福寿螺越冬。讨论了福寿螺对环境的适应能力和福寿螺北缘分布地区继续北移扩展的可能性问题。长江上游地区及湖南省福寿螺资源不仅增加湖北省福寿螺为害风险,而且增加湖北省福寿螺的防控压力。     

苹果实时荧光定量PCR分析中内参基因的筛选

【目的】为筛选苹果实时荧光定量PCR实验中最适内参基因,【方法】应用实时荧光定量PCR技术,分析5个传统内参基因18SrRNA、ACTB、GAPDH、UBQ、TUB在苹果不同基因型、不同组织、果实不同发育时期的mRNA表达差异情况。供试的6个不同基因型苹果分别为:新疆野生苹果、八棱海棠、丽江山荆子、‘津轻’、‘国庆’、‘金冠’;6种不同组织为果皮、果肉、叶片、愈伤组织、花瓣、种子;5个果实发育不同时期为花后28、50、74、95、115 d。【结果】经geNorm程序分析发现5种内参基因的表达稳定性各异,UBQ在果实不同基因型和不同发育时期的基因表达分析中最稳定;ACTB和UBQ在6种不同组织中表达均稳定。【结论】UBQ在参试样品中表达均比较稳定,是研究苹果基因表达分析中理想的内参基因。     

Expression of Mitochondria‐Associated Genes (PPARGC1A,NRF‐1, BCL‐2 and BAX) in Follicular Development and Atresia of Goat Ovaries

Most follicles undergo atresia during the developmental process. Follicular atresia is predominantly regulated by apoptosis of granulosa cells, but the mechanism underlying apoptosis via the mitochondria‐dependent apoptotic pathway is unclear. We aimed to investigate whether the mitochondria‐associated genes peroxisome proliferator‐activated receptor‐gamma, coactivator1‐alpha (PPARGC1A), nuclear respiratory factor‐1 (NRF‐1), B‐cell CLL/lymphoma 2 (BCL‐2) and BCL2‐associated X protein (BAX) played a role in follicular atresia through this pathway. The four mitochondria‐associated proteins (PGC‐1α, which are encoded by the PPARGC1A gene, NRF‐1, BCL‐2 and BAX) mainly expressed in granulosa cells. The mRNA and protein levels of PPARGC1A/PGC‐1α and NRF‐1 in granulosa cells increased with the follicular development. These results showed that these genes may play a role in the regulation of the follicular development. In addition, compared with healthy follicles, the granulosa cell in atretic follicles had a reduced expression of NRF‐1, increased BAX expression and increased ratio of BAX to BCL‐2 expression. These results suggested that changes of the mitochondria‐associated gene expression patterns in granulosa cells may lead to follicular atresia during goat follicle development.     

Effects of glucose and Mg2+ in the neurons damaged by glutamate

AIM and METHODS: To observe the effects of glucose-free and Mg²⁺-free in the extracellular fluid on the changes of [Ca ²⁺]_i in the cerebro-cortical neurons damaged by 1mmol/L glutamate using laser confocal scanning microscope. RESULTS: Both frequency and amplitude of neuronal calcium oscillation induced by glutamate were lowered in glucose-free and Mg²⁺-free buffers. The basic [Ca²⁺]_i concentration was lowered in the former case , but it was elevated in the latter case. CONCLUSION: Mg²⁺-free aggravates [Ca²⁺]_i overload induced by 1mmol/L glutamate ,under certain conditions the glucose-free might resist damage role of glutamate and Mg²⁺-free.