起始肥料对一品红生长的影响

 研究了生长介质中起始肥料对一品红生长的影响和一品红不同部位矿质养分含量。结果表明： 速效肥比缓效肥更有利于一品红生长并提高品质，速效肥中供试的两种NO₃^--N与NH₄⁺-N比例对一品红生长影响不大。绿色叶片矿质养分含量，除Fe和Mn较高外，与国外推荐的养分诊断指标相一致，说明目前国外推荐的一品红养分诊断部位适合于绿色叶片。     

不同培养条件对鲍鱼菇菌丝生长的影响

通过不同温度、pH值及培养基含水量处理 ,对鲍鱼菇菌丝生长状况进行了研究。结果表明鲍鱼菇菌丝生长适宜的温度范围为 2 0～ 31℃ ,最适温度为 2 5～2 8℃ ;pH值适宜的范围为 4 0～ 7 0 ,最适pH值为 5 5～6 0 ;培养基含水量适宜的范围为 6 0 %～ 80 % ,最适含水量为 80 %。     

氮素水平对单作和间套作小麦玉米叶片叶绿素含量及品质的影响

以间套作小麦玉米、单作小麦和单作玉米为研究对象,通过田间试验研究了氮素水平对单作和间套作小麦玉米叶片叶绿素及品质的影响。主要结果为:在同一施氮水平下,间套作小麦旗叶叶绿素含量大于相应单作;单作和间套作小麦开花期旗叶叶绿素含量和蛋白质含量、沉淀值之间都呈显著正相关(r分别为0.960*,0.948*,0.968*,0.957*)。在相同施氮水平下,单作玉米叶绿素含量高于相应间套作玉米;单作和间套作玉米孕穗期叶绿素含量与其蛋白质含量之间也呈显著正相关(r分别为0.861*和0.870*)。     

60%敌草隆·环嗪酮可湿性粉剂的高效液相色谱分析方法

反相高效液相色谱法测定60%敌草隆·环嗪酮可湿性粉剂有效成分含量,流动相为甲醇和水(57∶43),波长为254nm,环嗪酮和敌草隆的标准偏差分别为0.07和0.052;变异系数分别为0.53%和0.11%;平均回收率分别为98.9%和99.2%。线性相关系数分别为0.9999和0.9995。     

我国近年来水稻重大病虫害可持续控制技术重要研究进展——非化学控害技术研究

针对水稻病虫害防治中长期存在控害保产与生产无公害稻米矛盾比较突出的问题,研究提出了几种效果显著的非化学控害增产技术。其中,利用水稻遗传背景、对病虫抗感水平等差异显著的水稻品种多样性种植,控制稻瘟病的效果达42.12％～76.68％,抑制白背飞虱若虫数量增长效果明显,增产糯稻或优质稻600～1050 kg／hm²,平均增收约1 500元／hm²;稻鱼共育控制稻飞虱的效果为63.77％～86.89％,对纹枯病病株抑制率70.52％,控制稻田杂草效果为89.57％,平收获鲜鱼319.5～1 177.5 kg／hm²,水稻产量比对照区增产7.05％～10.11％;稻鸭共育控制稻飞虱效果63.73％～77.18％,控制稻螟效果30.11％,控制纹枯病效果19.33％～67.03％,对稻田杂草控制效果91.96％,减少施肥30.6％、农药59.3％,减少投入1 987.05元／hm²。     

兰州市SO_2污染控制区优化规划方案的探讨

根据《大气法》第二十七条关于划定酸雨控制区和SO2 污染控制区的规定 ,为使兰州市SO2 控制区达到环境质量目标的要求 ,本文以 98年的污染源资料和气象资料为模拟对象 ,利用大气扩散模式 ,通过各个污染源对每个控制点浓度分担率的计算 ,以污染源的总削减两最小 (总排放量最大 )或总削减率最小为优化目标 ,列出了几种优化方案并利用线性规划的方法对各种结果进行了对比分析。为了使最终的优化结果切实可行 ,将点源的上界乘一经济技术指标值 ,既可以使控制区达到环境质量目标值 ,又充分体现了公平合理的原则。     

内生拮抗枯草芽孢杆菌BS-2菌株的发酵条件

内生拮抗细菌BS 2菌株在以黄豆粉为原料的 3号培养基中生长速度快 ,发酵滤液对辣椒炭疽病菌的抑制作用强 ,菌液对辣椒果炭疽病的防效最好。培养基初始 pH值、培养时间、温度、通气量等对菌株生长及其抗菌物质的分泌有明显影响。结果表明 ,以黄豆粉培养基、初始 pH值 6 .7(灭菌后 )、2 8℃、培养 4 8h、并尽量增大培养通气量 ,为菌株的最佳发酵条件。     

Effect of EGFP gene transfection on the cell cycle distribution of primary cultured human chondrocytes

AIM: To investigate the effect of enhanced green fluorescence protein (EGFP) gene transfection on the cell cycle distribution of primary cultured human chondrocytes in order to establish a tracking method of cultured human nasoseptal chondrocytes. METHODS: pEGFP-N1 plasmid was amplified in E.coli, and purified by high purity kit. Primary cultured human chondrocytes,which were initially obtained from the nasoseptal cartilage, were cultured in vitro and transferred with pEGFP-N1 by means of electroporation with Amaxa nucleofector device. Transfering process and transient expression were evaluated by laser scanning confocal microscope (LSCM), the transfer efficiency and the cell cycle distribution were evaluated by flow cytometry. RESULTS: There was significant expression of EGFP at 24 h after transferring. The transfection efficiency of pEGFP-N1 into primary cultured human chondrocytes reached 35.37％ at 48 h. It didn't affect the process of cell adherance and had no effect on the cell cycle distribution. CONCLUSION: Primary cultured human chondrocytes, which were transfected with pEGFP, are alive in vitro, and the transferring process doesn't affect the cell cycle distribution. These results suggest that pEGFP-N1 is an ideal transient expression vector for primary cultured human chondrocytes and it might be a well tracer in construction tissue engineered cartilage.     

The ex vivo expansion characteristic of endothelial progenitor cells

AIM: To explore the ex vivo expansion characteristics of the endothelial progenitor cells (EPCs). METHODS: CD34⁺ cells were selected from umbilical cord blood mononuclear cells (MNC) by MiniMACS system, expanded at the same conditions as that for total MNC, coincubation of CD34⁺ and CD34^- from the same donation for EPCs. In addition, we tested the effect of vessel endothelial growth factor (VEGF) and passage on cell differentiation, expansion kinetics and apoptosis. EPCs were determined and quantified by immunocytochemistry and flow cytometry. RESULTS: Coculture of CD34⁺ and CD34^-,total MNC led to a significant increase in the expansion of CD34⁺ cells compared with CD34 enrichment (P＜0.05). There was a trend toward decreased apoptosis in cultures when early passage was performed once the linear cord like structures appeared. There was no significant effect on apoptosis between with VEGF and without VEGF group (P＞0.05). These differentiated EPCs were stained positive for CD34⁺, von Willebrand factor (vWF), KDR, CD31 and incorporate acetylated low-density lipoprotein (LDL). CD34⁺ and AC133⁺cells accounted for 68.2%±6.3% (n=6) and 57.2%±9.8% (n=6) of attaching (AT) cells at day 7 of culture, respectively. CONCLUSIONS: Coculture of CD34⁺ and CD34^- or culture of MNC enhances ex vivo expansion of EPCs. Early passage decreases apoptosis rate, VEGF has no significant effect on ex vivo expansion of EPCs.     

Effects of component of some Chinese herbs on proliferation of human umbilical vein endothelial cells in vitro

AIM: To observe the effects of some component of Chinese herbs for external use on proliferation of human umbilical vein endothelial cells (HUVEC) and investigate the mechanism of promoting tissue repair. METHODS: The method of MTT was used to examine the effects of Rg1, Rh1, perlolyrine, cinnamyl aldehyde, muscone, astragaluspolysaccharin (APS), velver antler polypeptide (VAP) and soluble extract of boswellia carterii birdw (BCB) on proliferation of HUVEC. RESULTS: APS did not promote proliferation of HUVEC at 9.75 mg/L-2.5 g/L; Rh1 promoted proliferation of HUVEC at 1.94 mg/L-0.5 g/L (P<0.05 or P＜0.01), and Rg1 inhibited proliferation of HUVEC at 31 mg/L (P<0.05); VAP promoted proliferation of HUVEC at 1 mg/L-0.5 g/L with optimal dose of 10 mg/L (P<0.01), Cinnamyl aldehyde promoted proliferation of HUVEC at 2 g/L(P＜0. 05); Muscone and soluble extract of BCB inhibited proliferation of HUVEC at 1 g/L, 0.5-2.5 kg/L(P＜0. 01), respectively; Perlolyrine inhibited proliferation of HUVEC at 0.125 g/L-0.5 g/L(P＜0. 01). CONCLUSION: The external herbs for supplementing Qi and warming Yang can promote HUVEC proliferation and improve angiogenesis during tissue repair. The external herbs for promoting blood circulation and accelerating capillary movement may have influence upon other stages of tissue repair.