维生素K3的合成及应用

本文概述了维生素K3的各种合成技术路线，对维生素K3生产技术的发展进行了展望，介绍了其应用和市场供求现状。     

优质籼型不育系Q2A的选育

Q2A是重庆市农业科学研究所和重庆市种子公司用金23B×中九B的F2代与58B×Ⅱ-32B的F2代杂交,再用复交F2代与珍汕97A杂交引入野败型胞质育成的一个优质籼型三系不育系,2003年7月通过重庆市科学技术委员会组织的技术鉴定.该不育系异交习性好;可恢性好,配合力强;米质优(12项测试指标中有7项达部颁一级优质米标准,5项达二级标准);苗瘟3级,叶瘟3级,颈瘟7级,对苗瘟和叶瘟表现为中抗,颈瘟感病.其与成恢047配组育成的优质杂交中籼新组合Q优5号米质优,产量高,抗稻瘟病,2003年12月通过重庆市农作物品种审定.     

硼浓度对毛木耳菌丝生长的影响试验

试验通过不同浓度的Na2B4O7在改变PDA培养基及棉子壳一木屑培养基的试验,测定了其对毛木耳菌丝生长的影响。结果表明:在200mg／kg浓度下促进作用最为显著,而其浓度超过400 mg／kg时对菌丝有强烈的抑制作用。     

维生素A水平对生长猪生产性能、肝脏维生素A含量和血清免疫参数的影响

试验研究饲粮添加不同水平维生素A(VA) (0、1300、2600、5000、10000、15000IU/kg)对22 -50kg生长猪生产性能、胴体品质、胴体无脂瘦肉增重、肝脏和血浆中VA含量、血清免疫参数的影响。结果表明 ,添加VA1300 -10000IU/kg 提高了日增重 (P>0.05)、极显著地降低料重比 (P<0.01) ;但VA添加水平从1300IU/kg增加至10000IU/kg,料重比显著提高 (P<0.05) ,采食量也极显著提高 (P<0.01)。各组屠宰率、瘦肉率、脂肪率、背膘厚、胴体瘦肉成分都无显著差异 (P>0.05) ,眼肌面积则随VA水平的升高而趋于增大(P>0.05)。胴体瘦肉和无脂瘦肉日增重在添加VA1300IU/kg 和10000IU/kg两组间很接近 ,而且优于其它组 (P<0.05)。随着VA水平的提高 ,肝脏中VA含量极显著提高 (P<0.01) ,至添加VA10000IU/kg组最高 ,之后略下降 ;添加VA有使血浆中VA含量升高的趋势 (P>0.05)。各组血清中IgG、IgA、IgM含量都无显著差异 (P>0.05) ,添加VA使T淋巴细胞中CD3+ 和CD8+ 亚群比例趋于升高 (P>0.05),随着添加VA水平提高 ,血清T淋巴细胞中CD4+/CD8+比值趋于下降 ,至添加VA10000IU/kg 组最低 ,在VA15000IU/kg 组又明显上升 (P>0.05)。以肝脏中VA含量为指标 ,生长猪VA适宜水平为在基础饲料上添加10000IU/kg ,但根据生产性能等其它指标 ,添加1300IU     

黑杨无性系日CO2固定总量的测定及与苗木生产潜势的相关性研究

通过对不同基因型黑杨无性系植株净光合速率日变化曲线与光合主体叶面积在时间和光强上进行累计积分来计算植株日CO2固定总量P。由于净光合速率日变化曲线不易准确测得，故以光响应曲线和光强的日变化来推测净光合速率日变化。对P值和生物量的相关性研究表明，二者的相关性很高。且认为可以用计算出的P值作为评估苗木生产潜势的指标之一，这为育种中生产力的早期选择提供了有力的证据。     

2型猪链球菌的血清学鉴定

本试验首次证实了２型猪链球菌在我国的存在，采用玻片凝集、琼脂扩散及毛细管沉淀等３项试验，对１９９０年以来广东某猪场断奶仔猪暴发流行的败血症、脑膜炎及关节炎病猪中分离的１５株链球菌进行了血清学鉴定。结果表明：１５株链球菌均为２型猪链球菌；用高压法提取抗原进行沉淀反应，其结果比酸热法提取抗原具有简便、敏感、特异性强的特点。     

In vitro expression and inhibition of procoagulant activity produced by bovine alveolar macrophages and peripheral blood cells

Local and systemic activation of coagulation is frequently associated with bacterial sepsis. The coagulopathy is due, at least in part, to expression of tissue factor (TF) by monocytes and macrophages. The purpose of this study was to evaluate the expression of procoagulant activity by bovine alveolar macrophages, leukocytes and platelets, and to determine the relative potency of three chemical inhibitors of TF expression (pentoxifylline, retinoic acid, and cyclosporin A). Bovine alveolar macrophages were stimulated with lipopolysaccharide (LPS) derived from Pasteurella haemolytica or recombinant bovine tumour nervous factor (TNF) and dose- and time-dependent effects on TF expression were studied. LPS and TNF induced TF expression in alveolar macrophages and LPS treatment of whole blood induced TF expression in mononuclear cells. Neutrophils and platelets also expressed procoagulant activity, but this activity was not inhibited by anti-bovine TF monoclonal antibody. Pentoxifylline (40 mol/L), retinoic acid (0.01 mmol/L) and cyclosporin A (0.08 mol/L) inhibited TF expression when added concurrently with LPS or TNF, but not when added 4 h after stimulation. TF mRNA was not detected in unstimulated alveolar macrophages by Northern blot analysis. In contrast, exposure to LPS or TNF for 6 h induced marked expression of TF mRNA, which was inhibited by treatment with pentoxifylline, retinoic acid and cyclosporin A. Expression of TNF by alveolar macrophages stimulated with LPS was also inhibited by these compounds. Our results indicate that procoagulant activity expressed by alveolar macrophages and monocytes is associated with expression of TF, whereas procoagulant activity expressed by neutrophils and platelets is not. The concentrations of pentoxifylline and retinoic acid necessary for inhibition of TF expression in vitro may not be achievable in vivo owing to their toxic effects. However, the in vitro concentration of cyclosporin A that inhibited TF expression did not exceed the plasma concentration observed in humans, and therefore may be useful for inhibition of TF expression in vivo.Abbreviations BAL bronchoalveolar lavage - LPS lipopolysaccharide - cDNA cloned deoxyribonucleic acid - cAMP cyclic adenosine monophosphate - GAPDH glyceraldehyde phosphate dehydrogenase - mRNA messenger ribonucleic acid - TF tissue factor - TNF tumour necrosis factor - DPBS Dulbecco's phosphate-buffered saline     

THE CLIMATE CHANGE AND FORESTRY OF HEILONGJI ANG PROVINCE IN 1990''''S

INTRODUCTIONIntheworldoftoday,theglobalclimatechangeanditsinfluenceonecologyhavebe-comeaveryimportantproblem,towhichmanyscientists,governnentleadersandordinarypcoplepaycloseattentionI1-'].Inl979,theWorldClimateResearchProgram(WCP)waslaiddowninthefirstworldclimatemeeting.lnl99(),thesecondworldclimatemeetingwasconvcl1edinGencva,andalltl1eexpertsagreedthattheglobalwarmlngwillbeextremelyseriousdisasterthananynatUralcalamityever.Attl1eMectingof"WorldEnvironmentandDevelopment,"holdinBrazil…     

Dynamics ofRhizoctonia solani (black scurf) in successive potato crops

The position of plants withRhizoctonia solani sclerotia (black scurf) on progeny tubers was mapped for an experimental field at Haren where potatoes were grown continuously and in rotation with other crops for five successive years, and for another field at Borgercompagnie with a 12 frequency of potatoes during three potato crops. Initially, the distribution of plants with black scurf on both fields was rather dense and homogeneous. In the following years the distribution became heterogeneous and patchy. The local decline ofR. solani AG 3 (the common potato pathogen) in Haren was apparently caused by an unknown factor selectively suppressingR. solani AG 3, while simultaneouslyR. solani AG 5 increased in mass. This AG 5 type proved to be an inferior competitor of AG 3 on the potato plant in a laboratory experiment. The specificR. solani antagonistVerticillium biguttatum did not play a role. A similar factor could have reduced the formation of black scurf in the experimental field at Borgercompagnie, whereV. biguttatum was also too infrequent to account for the decline.R. solani AG 5 was not present here and could not indicate the presence of a selective factor against AG 3.     

外源Ca2+ 和ABA 对高温下黄瓜花药中Ca2 + 、ABA及蛋白质合成的影响

 外源Ca^{2 +}能降低高温下黄瓜单核期花药的胞内Ca^{2 +}水平并提高花粉萌发率, 而ABA的作用与此相反。外源Ca^{2 +}和ABA处理能显著提高高温下黄瓜花药内源ABA的水平, 并产生新的蛋白质。以上结果表明, 高温下外源Ca^{2 +}可影响黄瓜花药内ABA信号系统, 继而可能改变基因表达, 并获得耐热性;外源ABA亦能影响黄瓜花药内Ca^{2 +}信号系统。