白蛾黑基啮小蜂种群数量变化规律的初步研究

选择徐州市林果场、云龙区和新沂市等受杨小舟蛾危害较重的不同类型杨树林分的未放蜂区(CK)和放蜂区,分别测定白蛾黑基啮小蜂在自然和人工释放2种状态下的种群数量变化。结果表明,该蜂林间自然种群数量以越冬代最高,对杨小舟蛾越冬蛹的寄生率高达(22.2±5.8)%,极显著高于第1~4代蛹(3.4%~6.4%);于越冬代和第2代害虫蛹期人工释放该蜂,释放后当代小蜂种群数量明显上升,可显著提高释放当代(越冬代和第2代)害虫蛹的寄生率,并对释放后各代害虫蛹具有一定的持续寄生效果;各代小蜂室温下的羽化进度均与相应世代寄主蛹发育进度相吻合。     

读者需求驱动的“五位一体”高校图书馆文献资源建设模式研究

为使图书馆文献资源建设更好的满足读者,提高读者使用资源的效率与满意度,通过文献调研法和问卷调查法对高校图书馆文献资源建设现状和读者需求情况进行调研分析,在此基础上构建出读者需求驱动的以OPAC查询、多渠道荐购、实体书店和电子资源4种渠道为主、文献传递和学科服务团队服务为辅的“五位一体”高校图书馆文献资源建设模式。总结模式的特点并辅以模式执行一段时间的数据统计。该模式五个环节应读者需求而生、为读者需求而动,互为补充,相互协调,系统地、全方位地满足了读者需求,并从该模式出发进一步探究高校图书馆文献资源建设未来发展方向。     

豫北山区“粮—草—羊”高效平衡养羊模式现状

从粮食作物、经济作物及饲草的种植,饲草料的加工调制与利用,全舍饲肉羊的养殖及杂交繁育,以及羊粪尿的资源化利用等方面介绍了豫北山区“粮—草—羊”高效平衡养羊模式发展现状,以期为促进豫北山区资源可持续利用、山区生态环境良性循环和社会经济可持续发展提供思路。     

光电开关在葡萄酒灌装系统中的应用

简述了光电开关的概念、工作原理、分类,总结了光电开关在全自动葡萄酒灌装系统中主要组成部分的实际应用效果,指出光电开关是保证葡萄酒灌装生产安全、顺畅、高效运转的有效手段。     

千岛湖国家重要湿地非生物资源及其利用调查

2009年10月～2011年10月,对千岛湖国家重要湿地非生物资源及其利用状况进行了调查.千岛湖湿地非生物资源有水资源、旅游资源、湿地岛屿和土地资源等,湿地蓄水总量178.4×108 m3,整体水质良好,全湖富营养化程度较稳定；旅游资源有8主类23亚类181种基本类型238个旅游资源单体,其中优良级旅游资源单体29个；湿地岛屿总面积5 954.53 hm2,其中林地面积5 913.80 hm2,非林地面积40.73 hm2;库尾和库湾季节性可耕地面积随水位变化在192.1 ～1 013.8 hm2间变化,千岛湖湿地非生物资源利用主要是水资源和旅游资源,湿地旅游已发展成为淳安县的经济支柱产业.     

基于MaxEnt模型的可可潜在适宜分布研究

根据野外采样和文献查阅,系统整理了可可的地理分布记录,并利用MaxEnt生态位模型和ArcGIS软件对可可的潜在适宜分布范围进行预测。结果表明:北美洲南部、中南美洲北部、非洲西部、亚洲东南部以及太平洋美拉尼西亚群岛地区均是可可的潜在适宜分布区域。其中,中国海南、台湾南部、云南西双版纳、广东雷州半岛也属于可可的适生范围。经ROC(Receiver operating characteristic)曲线分析法验证,MaxEnt模型的AUC(Area under curve)值为0.977,表明预测结果具有较高的可信度。各环境变量重要性的Jacknife检验表明,极端最低温度、年降雨量、年温度变化范围、最暖季降雨量对可可的潜在分布影响最大。     

HMGCR基因多态性与肉牛屠宰性状相关性分析

MHGCR是胆固醇生物合成过程中的限速酶,在内源胆固醇生物合成过程中起着重要的作用。研究以牛HMGCR基因为候选基因,采用PCR-SSCP和测序技术在利杂牛、利西杂牛、秦川牛、西杂牛和夏西杂牛五个群体共123个个体中检测遗传变异情况。结果表明,检测到AA和AB共2种基因型,没有发现BB基因型,测序分析发现一处SNP多态位点(GenBank:BC153262.1 11137TC)。不同基因型与屠宰性状的相关性分析显示,在利西杂群体中AA基因型个体与AB基因型个体相比,AA基因型个体的屠宰率和牛柳指标达到了极显著水平(P0.01),而AA基因型的上脑重显著高于AB基因型(P0.05),其余各项指标基因型间差异不显著(P0.05)。因此,HMGCR基因单核苷酸多态性对利西杂牛脂肪沉积有一定的影响,可作为影响屠宰性状的候选基因,指导肉牛的育种工作。     

Study on Expression and Preliminary Immunocompetence of CIC Protein Containing Molecular Adjuvants

To express CTB-IsdBid-Clfais(CIC) protein and evaluate its immunogenicity, CTB (as a molecular adjuvant) could be tandem linked with IsdBid-Clfais gene by the overlapping PCR method, then CTB-IsdBid-Clfais(CIC) was inserted into pET-32a(+) vector to construct recombinant plasmids pET-32a(+)-CTB-IsdBid-Clfais. The recombinant plasmids pET-32a(+)-CTB-IsdBid-Clfais were transformed into Escherichia coli (E.coli) BL21 to express the CTB-IsdBid-Clfa(CIC) protein, the CIC expression protein and its immune activity were detected by Western blotting and ELISA,respectively. The results showed that the length of CIC gene were 2 072 bp, and CIC was correctly inserted into the pET-32a(+) plasmids, the pET-32a(+)-CTB-IsdBid-Clfais recombinant plasmids were successfully constructed. Western blotting result confirmed that the molecular weight of CIC proteins was 95.9 ku, which were correctly expressed by E.coli BL21 with pET-32a (+)-CTB-IsdBid-Clfais plasmids. ELISA results showed that there was no significant difference among the CIC, IsdBid and Clfais protein groups (P>0.05), and there was extremely significant difference between CIC and BSA protein groups (P<0.01). In conclusion, the pET-32a(+)-CTB-IsdBid-Clfais recombinant plasmids were successfully constructed, CIC proteins were correctly expressed, and were able to react with serum from mice immunized with IsdBid and Clfais,respectively,therefore, CIC proteins had strong immune activity.     

红松无性系种子园与实生种子园种实性状观测

建立红松无性系种子园和实生种子园的实践证明:嫁接母树的结实株数、结实率、公顷产种量、种子千粒重等9项种实性状均优于实生母树,关键种实性状指标结实率、公顷产种量、出种率、种子千粒重、出仁率分别是实生母树的3.67倍、2.74倍、1.16倍、1.02倍和1.12倍.     

Effects of Smo gene silencing on cell activity and apoptosis of human cervical carcinoma HeLa cells

AIM: To investigate the effect of Hedgehog (Hh) signaling pathway on the viability and apoptosis of cervical carcinoma cells by shRNA technique to knock down Smoothened (Smo) gene. METHODS: Smo shRNA was used to transfect the cervical carcinoma HeLa cells. The expression of Smo and Gli1 at mRNA and protein levels in the HeLa cells was determined by RT-PCR and Western blot, respectively. The effect of Smo gene silencing on the growth of the cells was measured by MTT assay. The apoptosis and cell cycle were determined by flow cytometry. RESULTS: Compared with control group, the mRNA and protein expression of Smo and Gli1 were evenly reduced obviously after transfected with Smo shRNA for 72 h (P<0.05). The viability of HeLa cells transfected with Smo shRNA was significantly inhibited. The percentages of the cells in G₀/G₁ phase and early apoptosis rate were obviously higher in Smo shRNA transfection group than those in control group. CONCLUSION: Smo gene silencing effectively inhibits the cell growth and induces the apoptosis of human cervical carcinoma cells.