两阶抽样中比率型估计量的平均精度

本文给出了两阶抽样中总体均值的比率型估计量的平均精度,它当样本容量充分大时主项不劣于无偏估计量的平均精度．     

不同激素及其不同配比对绞股兰愈伤组织诱导的统计学分析

绞股兰的茎段和叶碎片外植体可在合适的激素调节诱导下形成愈伤组织．通过含有不同水平激素的MS培养基对绞股兰愈伤组织诱导试验,经统计学分析,可以找出对绞股兰脱分化形成愈伤组织细胞影响显著的激素及其适宜的激素水平．     

20-羟基蜕皮酮对蓖麻蚕蛹体液免疫的调节作用(英)

本研究指出20—羟基蜕皮酮(20-OHE)参加蓖麻蚕蛹对大肠杆菌的体液免疫反应。20-OHE的作用方式是多方面的,包括提高血淋巴蛋白质含量,产生抗菌蛋白,增加溶菌酶活性,和激活原酚氧化酶系统。这表明多个免疫控制系统参与蓖麻蚕蛹体液免疫反应的可能性。     

特种油料植物的种质资源研究

本文对特种油料植物的种质资源研究进行综述,这些植物包括含长链脂肪酸的Crambe,Limnanthes,Lunaria,短链脂肪酸的Cuphea,Lauraceae,羟基脂肪酸的Lesquerella,环氧脂肪酸的Vernonia,Stokesia,以及液体蜡酯的simmondsia等科、属的植物。     

新型气升式反应器在发酵培养中的应用研究

本文以Ｌ－苹果酸生产为例,采用新型的分段内循环气升式反应器分批培养产延胡索酸酶的产氨短杆菌ＭＡ－２,并与同等规模机械搅拌反应器中接着的结果相比较。数据表明,采用气升式发酵设备进行培养,该菌体的收率能提高近３％,且发酵周期能缩短一半左右,显著降低培养成本,该类型的反应器具有广阔的应用前景。     

生物制品检定动态管理系统的开发和应用

掌握生物制品的检定动态是质量管理的重要内容,由于检定周期随着制品种类、批数及检定条件的变化而变化,以往靠手工方式查阅繁杂的检定记录,难以随时快速、全面了解当时的检定状况。检定动态管理软件的开发可应用计算机自动跟踪显示检定进度和检定状态,及时反映制品质量和检定条件变化,明显提高了生产和质量管理部门的工作效率。     

马铃薯人工种子的研究

本研究以虎头（Ｈ）、克四（Ｋ）和Ｆａｖｏｒｉｔａ（Ｆ）三个品种的马铃薯不定芽在液体培养条件下诱导生成的微型薯为试材,经筛选后获得的大小一致的微型薯经过适度的低温处理后,用４％的海藻酸钠和２％的氯化钙溶液,在附加一定的植物激素条件下,进行人。种皮包埋形成人工种子。在无菌条件下,三个品种的人工种子萌发率均达９０％以上。在土壤中,人工种子萌发率可达６０％以上,萌发的人工种子中８０％能够形成生长发育正常的完整植株。     

REGULATORY ROLE OF 20-HYDROXYECDYSONE ON HUMORAL IMMUNITY IN THE PUPAE OF THE INDIAN SILKWORM,PHZLOSAMIA CYNTHIA RICINI*

Abstract The present study shows that 20-hydroxyecdysone(20-OHE) participates in the humoral immune responses of Philosamia Cynthia ricini, either normal or debrained pupae, to the E. coli. The mode of action of 20—-OHE is multiple. It raises hemolymph protein content, makes antibacterial proteins be produced, increases lysozyme activity, and activates prophenoloxidase system. It is possible that several immune control systems are involved.     

Cell cultures derived from early zebrafish embryos differentiate in vitro into neurons and astrocytes

The zebrafish is a polular nonmammalian model for studies of neural development. We have derived cell cultures, initiated from blastula-stage zebrafish embryos, that differentiate in vitro into neurons and astrocytes. Cultures were initiated in basal nutrient medium supplemented with bovine insulin, trout serum, trout embryo extract and fetal bovine serum. After two weeks in culture the cells exhibited extensive neurite outgrowth and possessed elevated levels of acetylcholinesterase enzyme activity. Ultrastructural analysis revealed that the neurites possessed microtubules, synaptic vessicles and areas exhibiting growth cone morphology. The cultures expressed proteins recognized by antibodies to the neuronal and astrocyte-specific markers, neurofilament and glial fibrillary acidic protein (GFAP). Poly-D-lysine substrate stimulated neurite outgrowth in the cultures and inhibited the growth of nonneuronal cells. Medium conditioned by the buffalo rat liver line, BRL, promoted the growth and survival of the cells in culture. Mitotically active cells were identified in cultures that had undergone extensive differentiation. The embryo cell cultures provide an in vitro system for investigations of biochemical parameters influencing zebrafish neuronal cell growth and differentiation.     

Spatial expression dynamics of Men-9 delineate the third floral whorl in male and female flowers of dioecious Silene latifolia

Sex determination in Silene latifolia is controlled by heteromorphic sex chromosomes. Female flowers have five fused carpels and ten arrested stamen primordia. The male-determining Y chromosome overrides female development to suppress carpel formation and promote stamen development. The isolation and characterization of two S. latifoliaM ale en hanced cDNAs, Men-9a and Men-9b, which probably represent different alleles of a novel gene are reported here. Men-9a and Men-9b share 91.8% coding sequence nucleotide identity, yet only 85.4% amino acid identity. The Men-9 cDNAs are related to the previously reported MROS3 cDNA from S. latifolia. However, MROS3 is not present in the S. latifolia population used in these studies and the expression dynamics of Men-9a and Men-9b contrast dramatically with those reported for MROS3. Men-9 cDNAs are expressed primarily in anthers of young male flowers, with highest expression in 1–2 mm buds. Men-9 expression is also observed at a low level in female flowers. In situ hybridization analysis reveals two phases of Men-9 expression. The first phase is during a common stage of early stamen development in male and female flowers prior to stamen arrest in female flowers. The second phase of Men-9 expression is maximal in the epidermis and endothecium of Y chromosome- and Ustilago violacea-induced stamens; expression in male and female flowers extends to the epidermis of the staminal nectaries with strict boundaries at the second and fourth whorls. Men-9 gene expression therefore delineates the boundaries of the third floral whorl in S. latifolia flowers.