农业信息平台虚拟化存储性能研究

文章从磁盘阵列技术及网络存储角度,针对农业信息平台虚拟化迁移进行存储设计,通过对磁盘阵列的主要性能进行分析和测试,结合农业信息平台、运行环境、数据结构以及存储需求进行试验设计,设计农业信息平台虚拟化迁移方案,并加以验证。     

毛皮动物犬瘟热、细小病毒性肠炎和脑炎防治技术指南

为了预防、控制和消灭毛皮动物犬瘟热、细小病毒性肠炎和脑炎,依据《中华人民共和国动物防疫法》及有关法律法规,制定毛皮动物犬瘟热、细小病毒性肠炎和脑炎防治技术指南,指导毛皮动物犬瘟热、细小病毒性肠炎和脑炎防控。     

草地早熟禾的选育研究与利用

内蒙古畜牧科学院草原所自 1985年以来 ,对从荷兰、美国、瑞典等国家引进的草地早熟禾 11个品种和国内采集的野生种进行了引种驯化 ,筛选出了瓦巴斯、凯达布鲁克茅 2个品种适应内蒙古地区的气候特点 ,是适宜推广种植的优良品种。利用国内野生种采用单株选择方法培育出了大青山草地早熟禾品种 ,它较原始群体抗性增强 ,叶量增加。目前已有较大的推广利用面积     

肉鹅H5亚型禽流感疫苗免疫效果的研究

选用H 5亚型禽流感油乳剂灭活疫苗(H 5N 1,R e1株)对马岗鹅作首免日龄、免疫次数与免疫剂量的免疫试验。结果表明,雏鹅在7、14或21日龄作1次免疫均产生免疫应答,其中14与21日龄免疫组免疫后第5周抗体水平均达4 log2以上,抗体动态变化均值与峰值均高于7日龄免疫组2~3个滴度。用0.5、1和2 m l/只3个剂量对14日龄雏鹅的免疫试验中,0.5m l组抗体水平上升过程缓慢,免疫后4周抗体水平才达4 log2以上,1与2 m l组在免疫1周后上升速度较快,免疫后2周即达4 log2以上,抗体水平相近,但2 m l免疫组免疫后5~7周抗体水平均低于1 m l免疫组。说明接种剂量为1或2 m lH 5N 1油苗比接种0.5 m l的免疫效果好,尤以1 m l免疫剂量效果最好。雏鹅在7、14日龄或14、21日龄作2次免疫和7、14、21日龄作3次免疫,首免后抗体上升速度快,各检测点抗体水平均值相近,均在首免后3周达到4 log2以上,4~5周达6 log2以上,4~7周的抗体水平均高于14日龄1次免疫组,且提前2周达到4 log2以上,说明2次、3次免疫组的抗体水平高于1次免疫组,而2次与3次免疫组的抗体水平无明显差异。以上结果说明,在肉鹅生产的禽流感免疫中,选择以14日龄首免0.5 m l/只,21日龄2免接种1 m l/只可取得较为理想的免疫效果。     

杀菌剂啶菌噁唑的高效液相色谱分析

建立了一种用反相高效液相色谱测定啶菌噁唑的定量分析方法。采用C18ODS色谱柱,以甲醇-水(75∶25,体积比)作为流动相,流速1.0mL/m in,检测波长220nm。啶菌噁唑色谱图显示两个吸收峰,分别为两个同分异构体Z体和E体。在400700μg/mL浓度范围内,标准溶液浓度和吸收峰面积之间有良好的线性关系,回归方程为Y=4.846 7x+232.85,相关系数r为0.999 2;对原药溶液及其制剂溶液测定的重复性SR分别为0.004 0和0.004 7。该方法准确、精密,适用于啶菌噁唑的定量分析。     

高效毛细管电泳同时测定4种氟喹诺酮类抗菌药

建立同时测定4种氟喹诺酮类抗菌物(左氧氟沙星、培氟沙星、沙拉沙星和洛美沙星)的高效毛细管电泳(HPCE)法。考察了缓冲液离子浓度和pH、分离电压、运行温度等电泳参数,确立了最佳的电泳条件:缓冲液为10 mmol/L磷酸二氢钾-20 mmol/L硼砂(pH9.0,内含35mmol/L SDS),紫外检测波长278 nm,分离电压28 kV,运行温度25℃。结果表明,4种药物在8min内得到完全分离,分离度R为1.2以上。方法精密度(RSD)为0.22%~0.26%(迁移时间)和1.36%~2.39%(峰面积),回收率99.60%以上。该法快速、简便、准确。     

微量元素硒对成年皖西白鹅输卵管膨大部粘蛋白的影响

应用组织化学PA S-AB染色和定量图像分析法,研究了不同水平微量元素硒对成年皖西白鹅输卵管膨大部粘蛋白的影响,结果表明:日粮中添加0.2 m g/kg微量元素硒鹅输卵管膨大部粘蛋白与对照组(不加硒)差异显著(P<0.05);日粮中添加0.60 m g/kg与对照组差异极显著(P<0.01);当日粮中添加硒到1.1 m g/kg时,与对照组差异不显著(P>0.05);说明随着硒添加量的加大,皖西白鹅会发生慢性中毒。因此,微量元素硒对成年皖西白鹅输卵管膨大部粘蛋白的影响有显著差异。     

4味中药及其与抗菌药的复方制剂的MIC测定

用改进的试管两倍稀释法测定了黄连、鱼腥草、大青叶和苦参4味中药及其相互配伍（1：1）对标准大肠杆菌的最小抑菌浓度和4味中药与抗菌药配伍（1000：1）对临床分离鸡大肠杆菌的最小抑菌浓度。结果表明，4味中药及其相互配伍对大肠杆菌标准株有一定的抑制作用，其MIC值介于3．91—62．50mg／mL之间，其中大青叶和鱼腥草以1：l配伍对大肠杆菌抑菌效果最好，MIC为3．91mg／mL；对临床分离株，单方药中黄连抑菌效果最好，MIC为31．25mg／mL，24种复方药中，黄连和盐酸多西环素或加替沙星以1000：1配伍的抑菌效果最好，其MIC为3．91mg／mL。     

Prevention of isinglass on the chronic atrophic gastritis in rats and its mechanism

AIM: To evaluate the effect of isinglass on chronic atrophic gastritis(CAG) in rats and its mechanism. METHODS: An animal model of CAG in accordance with the previous experience of combined administration of 60% ethanol, 20 mmol/L sodium deoxycholate and 0.1% ammonia water was established in SD rats. Isinglass was used as preventive therapy while we were establishing CAG rat model. Finally all the rats were executed and pathologic changes of the gastric mucosa were studied by gross appearance and microscopy and serum epidermal growth factor (EFG) and growth hormone(GH) contents were tested. RESULTS: In each isinglass prevention group, inflammation grade of gastric antrum was less than that in model group (P<0.01) while the mean ratio of the thickness of gastric mucosal gland and muscularis mucosa (L1/L2), the number of gastric glands in 1 mm lengths of mucosal layer in longitudinal sections were much better than those in model group (P<0.01).They were very close to normal control group (P>0.05). The expression of proliferating cell nuclear antigen (PCNA) in gastric mucosa and serum EFG level were higher than those in model group (P<0.01, P<0.05), but serum GH content showed no different between isinglass prevention group and model group. CONCLUSION: Isinglass preventes the gastric mucosal atrophy in the CAG model. Its mechanism may be related to the effects of decreasing the gastric mucosal damage， promoting the cell proliferation and increasing of internal EFG secretion.     

Effect of rhEGF activating extracellular signal-regulated kinase on the expression of Bcl-2 and p53 protein in human amniotic cells

AIM: To explore the effect of recombinant human epidermal growth factor (rhEGF) on the ERK1/2 pathway and its safety in use when the proliferation of cultured FL cells (human amnion epithelial cells) were promoted by rhEGF.METHODS: FL cells were stimulated by rhEGF at various concentrations.The proliferation rate of FL cells was evaluated by MTT assay.Western blotting was used to detect phosphorylation of ERK1/2 (p-ERK1/2) and the change of Bcl-2 and P53 protein.RESULTS: The proliferation rate FL cells reached the maximum when the concentration of rhEGF was 10 μg/L (42.4％，P<0.01).Western blotting showed that the activity of p-ERK1/2 increased significantly when rhEGF ranged in 10 μg/L to 60 μg/L.Level of Bcl-2 was unchanged in each groups.Level of P53 decreased significantly when the concentration of rhEGF was 60 μg/L.CONCLUSION: It is safe when rhEGF presents in optimization concentration of 10 μg/L.The capability of apoptosis may be depressed when rhEGF is in larger dose.