都市餐饮企业的净菜需求影响因素分析——以北京市为例

净菜的广泛使用能提高餐饮企业的出餐率,减少其后厨面积、劳动用工和厨余垃圾。基于北京地区708份餐饮企业净菜需求的问卷调查样本,运用垄断竞争市场理论和二元选择模型分析了影响餐饮企业净菜使用行为的具体因素。研究发现,对净菜了解程度不够和净菜价格偏高是制约餐饮企业使用净菜的主要因素,具有不同个体特征和环境特征的餐饮企业选择净菜的倾向性不同。建议在餐饮业大力开展净菜宣传科普工作;大力扶持净菜加工企业和发展相关技术支撑体系以降低净菜价格。     

乡镇图书馆(室)要加强对农村读者的服务

本文通过对农村读者的调研 ,提出了农村读者读书难 ,以及他们对具体书刊的需求。着重要求乡镇图书馆加强对农村读者的服务 ,提高农村读者的文化素质。并针对实际提出解决问题的服务对策。     

土壤养分位与广义氧化还原电极电势

 根据广义氧化还原理论,给出了土壤溶液中NH₄⁺,P,Ca等养料成份的广义氧化还原电极电势。与养分位比较,用广义氧化还原电极电势来量度土壤养分有效度具有较多的优越性。     

岭西电网经济分析

本文对岭西电网的经济运行调整进行了分析、总结。并应用《岭西电网经济运行计算》系统的计算结果，提出了岭西电网的经济运行调整办法。     

浊度法测定维生素C注射液细菌内毒素含量

应用BET-32型细菌内毒素测定仪定量测定维生素C注射液的细菌内毒素含量，干扰试验表明，维生素C注射液在400倍稀释时，测定内毒素的干扰最小。7个不同批号的维生素C注射液测定结果显示，7批的回收率均符合测定要求，其中4个批号的人用维生素C注射液内毒素含量符合药典标准，兽用3个批号产品的内毒素含量偏高。     

黄麻（新、引进）品种在闽南地区的产量（鉴定）试验

通过对中国农科院麻类所新选育的3个黄麻圆果种和12个国外引进的黄麻优异品种进行2002-2005年品种比较试验，结果表明：C90-2、C90-6、C89-6比对照种粤圆五号增产14．97％-19．34％，均达极显著水平。O-3、O-1、O-3（红茎）比对照种宽叶长果增产32．02％-34．21％，均达极显著水平。O-4（Ⅱ）比对照种增产12．28％达显著水平。C-1、C-5比对照种粤圆五号增产11．90％和7．82％。且主要经济性状优良，抗病力强。黄麻品种C90-2、C90-6、C89-6、O-3、O-1、O-3（红茎）、0-4（Ⅱ）、C-1和C-5适合于福建闽南麻区推广种植。     

‘三棱榄''橄榄果实香气成分分析

1 材料与方法选取广东优良鲜食橄榄品种‘三棱榄’,2001年12月6日采样,采用固相微萃取法(SPME)富集香气成分(鲜橄榄果肉于15℃下捣碎后取样1.0 g放入4 mL聚四氟乙烯硅橡胶垫密封螺口玻璃瓶中,插入100μm聚二甲基硅氧烷纤维头于室温25-30℃顶空取样2 h),用美国Finnigan TRACE GC-MS气相色谱-质谱联用仪进行分析。气相色谱柱为DB-1弹性毛细管柱30 m×0.25 mm,载气为He(99.99％),流速1.0mL/min。程序升温从40℃开始先保持10 min,后以2℃/min的升温速率升至150℃保持10 min。质谱条件:电子能量70 eV,离子源温度250℃,质量范围35-450 aum,不分流进样。2002年12月18日采样重复分析。     

Influences of chronic hypoxia on the gene expression of Kv1.3,Kv2.1 and Kv3.1 induced by acute hypoxia in PASMC of rats

AIM and METHODS: Total RNA was extracted from 6th rat subcultured pulmonary artery smooth muscle cells(PASMC) exposed to continual chronic hypoxia or normoxia and the effects of chronic hypoxia on the changes of Kv1.3,Kv2.1,Kv3.1 mRNA in cultured PASMC induced by acute hypoxia were studied by semiquantitative RT-PCR in vitro. RESULTS:①Kv1.3,Kv2.1,Kv3.1 genes were found to be expressed in PASMC of rats exposed either to hypoxia or normxia.②The expression of Kv2.1 and Kv3.1 in 6th subcultured of PASMC in normaxia group could be upregulated by exposure to acute hypoxia,the levels of Kv2.1 and Kv3.1 mRNA were significantly increased from 0.646±0.092, 0.782±0.104 to 1.059±0.134, 0.985±0.116,respectively (P<0.01,n=5). ③PASMC cultured continuously in chronic hypoxia for 6 subcultures and then exposed to normoxia for 12 h,thereafter the expression of Kv2.1 and Kv3.1 were downregulated by acute hypoxia for 6 hours.The level of Kv2.1 mRNA was significantly decreased from 1.008±0.117 to 0.649±0.097 (P<0.01,n=5). CONCLUSION:Kv2.1,Kv3.1 genes might be oxygen sensitive genes.Chronic hypoxia might change the response of these Kv genes of PASMC to acute hypoxia and down-regulate its expression,which might probably decrease the role of Kv in HPV.     

Roles of the Kv1.2, Kv1.5, Kv2.1 potassium channels in hypoxia pulmonary vasoconstriction

AIM: To determine the role of Kv1.2, Kv1.5, Kv2.1 in the hypoxia pulmonary vasoconstriction (HPV). METHODS: Male Wistar rats were divided into two groups: normoxic group and hypoxic group. The single smooth muscle cell was obtained from pulmonary artery of Wistar rats with acute enzymatic digestion method. The conventional whole-cell patch clamp technique was used to record the resting membrane potential (Em) and the potassium currents of voltage-gated potassium channel (IKv) in rat pulmonary arterial smooth muscle cells (PASMC). Intracellular application of Kv1.2/Kv1.5/Kv2.1 antibodies (1∶125) was conducted through the whole-cell patch clamp system. RESULTS: ① Em of PASMC was depolarized after 24 h hypoxia compared with that of control cells . IKv of PASMC was decreased after 24 h hypoxia, . ② The mixture of Kv1.2/Kv1.5/Kv2.1 antibodies depolarized Em and inhibited IKv in PASMC from normoxic rat, whereas the mixture of Kir2.1/Kir2.3/Kir4.1 antibodies had no effects on them. ③ The mixture of Kv1.2/Kv1.5/Kv2.1 antibodies and the mixture of Kir2.1/Kir2.3/Kir4.1 antibodies had no effects on IKv and Em from rats hypoxic for 24 h. CONCLUSION: Kv1.2, Kv1.5, Kv2.1 might be oxygen sensitive potassium channels which mediated HPV.