等值线制图工具 Surfer在病虫测报上的应用研究

Surfer系统是美国金软公司开发的专门制作等值线的工具。1997年以来,笔者对其运用于稻飞虱等农作物病虫害的监测方面作了探讨和开发。阐述了病虫分布图的绘制和遮盖图编制的过程和方法。     

特种脱水蔬菜研究进展

综述了国内外特种脱水蔬菜的生产状况和趋势，特种脱水蔬菜的加工技术，特种脱水蔬菜生产成果及展望。     

羊肚菌研究进展

综述了近年来羊肚菌营养成分、有效成分，培养技术，以及细胞学、生物化学和分子生物学等方面的研究进展。     

姬松茸与双孢蘑菇不同菌株的RAPD扩增研究

以4个姬松茸菌株和2个双孢蘑菇菌株为材料，用20个随机引物对它们进行RAPD扩增，通过对供试菌株遗传相似系数的估算和系统聚类分析，构建姬松茸和双孢蘑菇遗传相关树状聚类图谱，结果表明，进行RAPD扩增的20个随机引物中，有12个能产生三种带型，当遗传相似系数升至0.8713时，这6个菌株被分为3类，第一类为菌株18和26，第二类为菌株13和12，第三类为菌株33和45。     

大豆疫病的种子处理技术研究

本试验用不同浓度的瑞毒锰锌、杀毒矾和克露进行大豆种子处理试验，结果表明，５００ｐｐｍ瑞毒锰锌对大豆疫病具有很好的治疗作用，而用杀毒矾以种子重量０．４—０．５％的剂量闷种，能显著地抑制大豆疫霉菌的侵入     

补铬对热应激蛋鸡肾上腺组织结构的影响

试验选择处于热应激条件下的192只35周龄新罗曼褐壳蛋鸡,随机分为6组,分别饲喂添加0.10,20,30,40,50 g/t含铬量为7.410mg/kg的葡萄糖耐量因子(GTF)的玉米—豆粕型基础日粮52d。试验结束时随机抽取试验鸡36只(每组6只),取肾上腺称重并制作切片,研究有机铬对热应激蛋鸡肾上腺组织结构的影响。结果试验组肾上腺重量较对照组略有增加;热应激时蛋鸡肾上腺的肾间组织比例增大,肾间组织和嗜铬组织的细胞均有结构受损的现象;补铬使肾间组织比例减小,嗜铬细胞增多,细胞结构完好。     

君子兰转化酶基因片段(CMCW1)的克隆和序列分析

 分析植物酸性转化酶基因的保守区序列，设计一对PCR引物，以君子兰基因组DNA为模板，采用PCR方法扩增出长约500 bp的DNA片段，克隆入pGEM-TEasy载体，测序结果表明获得君子兰酸性转化酶基因家族的一个成员CMCW1，该基因片段长518 bp，不含内含子，编码172个氨基酸。其序列已在GenBank中登记(登记号为AY151269)。在GenBank中进行同源性检索的结果表明，该成员编码的氨基酸与其它植物细胞壁酸性转化酶编码的氨基酸同源性较高。     

棉花调亏灌溉的生理基础研究

以盆栽棉花为材料,通过苗期和现蕾期不同程度的亏水处理(低、中、高三个水平),对调亏灌溉节水效应及生理机制进行了研究。结果表明:适时适度的水分亏缺可使植株旺盛的营养生长得以有效控制,株型和根冠比都更为理想。调亏期间,蒸腾速率和气孔导度都明显下降,而光合速率下降不明显,复水后光合速率和气孔导度明显恢复且接近或高于对照;此外,水分亏缺不仅影响棉桃的数量,而且影响单果重。表明适度的亏水处理可使水分利用效率明显提高,而经济产量接近或高于对照,同时节水20%以上。     

Model establishment and biological behaviour observation of mouse blastocyst co-cultured with hepatocarcinoma cell lines with differently invasive and metastatic potential in vitro

AIM: To explore interaction and biological behaviour changes of two kinds of cells-blastocysts and hepatocarcinoma cells in the same microenvironment. METHODS:The models of mouse blastocysts co-cultured with human hepatocarcinoma cell lines were established, then biological behaviours and mutual effects of the two kinds of cells in co-culture system were observed. RESULTS: Compared with control group, hepatocarcinoma cells with differently invasive and metastatic potential significantly enhanced the rates of blastocyst hatchment , attachment and outgrowth(P＜0.05). There was no significant difference in those among hepatocarcinoma cells co-cultured groups (P＞0.05). The blastocyst hatched and attached to hepatocarcinoma cells with differently invasive and metastatic potential. Then, differential trophoblasts invaded hepatocarcinoma cells. The clear-cut interfaces were gradually formed between both sides. Hepatocarcinoma cells on interface showed changes of growth direction and cell shapes and did not invade blastocysts. CONCLUSIONS: Hepatocarcinoma cells promoted blastocyst development. Blastocysts implanted and invaded hepatocarcinoma cells with differently invasive and metastatic potential in vitro, which indicate that blastocyst implantation in vitro does not relate with the kinds and differential level of interactional cells and the low selectivity maybe relate with high adaptability of early life.