玉米螟赤眼蜂适宜生境的研究与利用:Ⅲ.夏玉米间作匍匐型绿豆对赤眼蜂的增诱作用及其在穗期玉米螟防治中的利用

本文就夏玉米间作匍匐型绿豆对玉米螟赤眼蜂增诱作用及其在穗期玉米螟防治中利用的可行性进行了研究。结果表明，夏玉米间作匍匐型绿豆结合接种式放蜂区，与平作夏玉米结合接种式放蜂区和不放蜂对照区相比，明显提高了玉米螟赤眼蜂对螟卵的寄生率，１９９２年三者人工挂卵的卵块总寄生率分别为２６．７％、３．６％和０；１９９３年分别为２８．０％、６．６％和１．０％，自然落卵的寄生率分别为６９．１％、２２．４％和４．６％。１９９４年用心叶期抗螟品种间作绿豆结合接种式放蜂区，人工挂卵的卵块总寄生率为３０．７％，而平作夏玉米不放蜂对照区仅为２．５％；自然落卵的卵块寄生率前者为５６．２％，后者为１２．３％。心叶期抗螟品种间作匍匐型绿豆结合接种式放蜂区、心叶期抗螟夏玉米平作不放蜂和感螟品种不放蜂对照区的平均百株蛀孔数分别为５４．８、１０２．６和２７７．２个，放蜂区与两个不放蜂对照区相比，对玉米螟的防效分别为４６．６％和８０．２％。试验结果显示采用心叶期玉米抗螟品种间作匍匐型绿豆，并接种释放少量赤眼蜂等综合措施对穗期玉米螟害有明显的控制作用     

白菜镉积累基因型差异研究

 采用87 个白菜品种, 于春夏和秋冬两生长季节在镉(Cd) 污染土壤中进行植株地上部Cd 积累差异研究。结果表明, 不同品种间镉含量存在极显著差异, 且春夏季高于秋冬季。     

黄瓜前中期染色体C - 分带及其制备方法研究

 以活体种子根为材料, 采用放线菌酮预处理, 直接获得了清晰的黄瓜前中期染色体C - 分带。黄瓜前中期染色体的长度介于3～8μm , 单套染色体组具有21 条稳定的C - 带, 包括12 条末端带、7 条着丝点带、1 条中间带和1 条随体带。还探讨了影响前中期C - 分带制备的关键因素, 提出了黄瓜前中期染色体C - 分带的实用制备方法。     

利用废菌糠提高覆土持水力和蘑菇产量的研究

本文利用平菇等食用菌的废菌糠 ,经适当无氧发酵等一系列处理后添加到普通泥土中 ,使其最大持水力提高至 5 1 3% ,单产提高 13 6 %     

三尖杉枝叶粉末防治花生根结线虫病

采用盆栽及大田小区试验,研究了三尖杉Cephalotaxus fortunei枝叶干粉末对花生根结线虫病的防治效果.盆栽试验结果表明,每盆(2kg土)施用三尖杉枝叶干粉末10、15及20 g三种处理,与对照组相比,初侵染相应推迟4、6、10天,并能减少侵染量,降低根结增长率,显著减轻花生根结线虫病病情.大田小区试验结果与盆栽试验结果相似,每小区(5m2)沟施三尖杉枝叶干粉末120、80、50 g,处理后34及53天的2次平均防治效果分别为89%、82%及50%,施药对照10%益舒宝颗粒剂25g处理(相当于45kg/hm2)为74%.综合使用剂量及花生生长情况,建议沟施150kg/hm2三尖杉枝叶干粉为宜.     

黄瓜花叶病毒丹参分离物的鉴定和外壳蛋白基因序列分析

 丹参(Salvia miltorrhiza Bge.)为唇形科鼠尾草属草本植物,以根入药,是我国一种常用大宗中草药。近年来河北安国中药材基地丹参上一种退化病十分严重,该病田间发病率高,有的田块高达60%~80%,表现为花叶、斑驳、卷叶、黄化、矮化等症状,严重影响了丹参的产量和品质。我们利用生物学、电镜观察、血清学方法和基因序列测定等方法对病原进行了初步研究,发现黄瓜花叶病毒(Cucumber mosaic virus,CMV)与该病害密切相关     

茭儿菜(野茭白)的生物学特性

茭儿菜 ,别名野茭白、野茭瓜 ,属禾本科菰属。须根系 ,茎分地上茎和地下茎 ,叶分叶鞘和叶片两部分 ,圆锥状花序 ;茭儿菜在春季发芽、生根 ,随温度升高生长加快 ,夏、秋季抽穗、开花、结实 ;以地下匍匐茎和地上茎作为繁殖材料 ,生长发育对环境条件的要求 :适温范围 10～ 2 8℃ ,生长期间不能缺水 ,需 2 5～ 5 0cm深厚土层 ,以粘壤土或壤土为宜 ,生长期间需要充足的阳光 ,不耐遮荫     

Regulation of MMP-2 and TIMP-3 expression by uPA signal transduction system in human bone giant cell tumor

AIM: To study effects of urokinase-type plasminogen activator (uPA) signal transduction on expression of matrix metalloproteinase-2 (MMP-2) and tissue inhibitor of matrix metalloproteinase-3 (TIMP-3) in giant cell tumor of bone (GCT). METHODS: Expression of uPAR, MMP-2 and TIMP-3 in GCT tissue was detected by immunohistochemistry. Phosphorylation level of mitogen-activated protein kinase (p44) in uPA/uPAR signal pathway in cultured GCT cells was detected by immunoprecipitation. The expression of MMP-2 and TIMP-3 in cultured cells after treatment with uPA-ATF or anti-uPAR antibody was also detected by Western blotting. RESULTS: 1) Urokinase-type plasminogen activator receptor (uPAR) was positive on the cell membrane and in cytoplasm of some mononuclear stromal cells (MSCs) and multinucleated giant cells (MGCs); 2) MMP-2 was positive in the cytoplasm and on the cell membrane of almost all of MSCs and some of MGCs. The polar distribution of MMP-2 in the cytoplasm of MGCs was especially obvious; 3) The expression of TIMP-3 of some MSCs and MGCs in GCT was much lower than MMP-2. The positive signal also showed a prominent polarity; 4) After treatment with uPA-ATF, the phosphorylation level of p44 in GCT cultured cells was much higher than the control. Addition of anti-uPAR antibody in the cells remarkably down-regulated the phosphorylation level of p44 as compared with the control group, suggesting that uPA-ATF participates cell signal transduction and this reaction can be inhibited by anti-uPAR antibody; 5) uPA-ATF cell signal pathway up-regulated expression of MMP-2 and TIMP-3, while anti-uPAR antibody down-regulated the expression of MMP-2 and TIMP-3. CONCLUSION: These results demonstrate for the first time that uPA-ATF directly regulates the expression of MMP-2 and TIMP-3 by signal transduction pathway, and the over-expression of MMP-2 and TIMP-3 may play an important role in local osteolysis of GCT.     

扫描昆虫雷达实时数据采集、分析系统

利用自行设计、制作的扫描昆虫雷达数据采集分析系统,对扫描雷达回波的VGA图像信号进行单帧采集和多幅序列采集,经过图像处理、参数自动识别和回波的自动分析、计算后可得到昆虫活动的方位、高度、距离、密度、飞行的方向和速度等一系列迁飞活动数据。对迁飞昆虫活动实时监测,实现该类害虫的准确预测和有效治理具有非常重要的作用。     

Effects of changing PKC activity on proliferation and telomerase expression in human hepatocellular carcinoma cells

AIM: To investigate whether protein kinase C (PKC) is involved in the proliferation and the telomerase expression in human hepatocellular carcinoma cells. METHODS: Human hepatocellular carcinoma cells (BEL-7402) were treated with exogenous phorbol-12-myristate-13-acetate (PMA, PKC activator) and staurosporine (SP, PKC inhibitor) for 48 hours. The techniques of cell culture and the telomeric repeat amplification protocol silver staining in combination with computer image scanning system in vitro were used to observe the variations of the growth and the telomerase expression. RESULTS: The proliferative potential of BEL-7402 cells was decreased by the action of PMA as well as SP, and the telomerase expression was also inhibited by PMA and SP. CONCLUSION: Our findings suggest that the proliferation of human hepatocellular carcinoma cells and the telomerase expression may be related to PKC.