内蒙古典型草原地区常见植物光合、蒸腾速率和水分利用效率的比较研究

在所测78种植物中，光合(Ph)、蒸腾速率(Tr)和水分利用效率(WUE)的平均值，分别以反枝苋、藜和西伯利亚滨藜最高。在不同分类系统中，Ph、Tr和WUE个指标，C4植物大于C3植物；双子叶植物通常大于单子叶植物；藜科植物高于其他科植物；1—2年生草本高于其他生活型植物；撂荒地植物一般高于其他植被类型的植物。方差分析表明，光合速率的差异显著性水平在各分类系统中均高于蒸腾速率和水分利用效率。     

福建峨嵋峰自然保护区资源现状与评价

通过对福建峨嵋峰自然保护区资源的综合调查，对该保护区的资源种类，分布特点等进行全面阐述，并进行了分析评价。     

黄土高原水土保持世行贷款项目区局地气候变化初步分析

对黄土高原水土保持世界银行贷款项目实施前后的监测数据和有关气象资料进行分析表明 ,大规模林草、梯田等坡面措施和沟道坝库工程的实施 ,影响了当地小气候特性 ,较好地起到了调节温度、提高湿度、增加降水和雾日、减少冰雹等作用 ,项目区与参照站比较 ,相对湿度提高了 5～ 10个百分点 ,平均每年有雾日相对增加了 6 7d ,年降水量相对增加 5 %～ 10 %。     

桑椹红色素稳定性的研究

研究了光和热等物理因素、常用食品添加剂、金属离子、氧化剂及还原剂对桑椹红色素稳定性的影响。结果表明 :pH值对桑椹色素的影响显著 ,在酸性条件下色素稳定 ;长时间高温和光照对色素有明显的破坏作用 ;金属离子Na+ 、Ca2 + 、Cu2 + 、Fe2 + 、Mg2 + 、Zn2 + 和Mn2 + 对桑椹色素色泽有一定的增色效果 ,但Fe3 + 则有明显的不良影响 ;食品中常用的葡萄糖、蔗糖、苯甲酸钠和山梨酸钾对桑椹色素无明显的不良影响 ;VC对桑椹色素有双重作用 ,而H2 O2 和Na2 SO3 对色素有严重的破坏作用。     

毛竹林丰产技术标准推广应用成效的评析

介绍尤溪县实施《毛竹丰产林标准化示范县》所取得的成效及采取的主要措施,并提出今后竹业发展的工作思路。     

家蚕血液、消化液中酸性核糖核酸酶和天冬酰胺酶活性的初步研究

测定了家蚕夏芳、长灰A和大造各品种血液、消化液中酸性核糖核酸酶及家蚕秋白、夏芳、长灰A和大造各品种天冬酰胺酶性变化。结果表明：各品种血液、消化液中酸性核糖核酸酶、天冬酰胺酶活性变化随发育呈现较强的规律性，血液中，4龄第3d、5龄第3d这两种酶均出现峰值，4龄眠前活性较低，消化液中，5龄第3d这两种酶活性均较高，不同品种这两种酶活性峰值出现时间有差异；各品种血液中酸性核糖核酸酶、天冬酰胺酶性均明显高于相应品种消化液中这两种酶活性；各品种之间血液、消化液中这两种酶活性有明显差异。     

多年生黑麦草顶峰的引种适应性研究

国外引进优良草坪草种———多年生黑麦草顶峰 (Pinnacle) ,在国内的 3个气候带 :北京 (北过渡带 )、兰州 (寒冷半干旱带 )和成都 (南过渡带 )等地 ,进行了品种评定和适应性的研究 ,结果表明 :多年生黑麦草顶峰适宜在中国北方过渡带和南方夏季不甚高温高湿的地区推广 ,在兰州以西越冬不理想。     

交播技术在园林草坪养护中的应用研究

在过渡气候带的园林绿地，进行了暖季型草坪秋季交播多年生黑麦草籽的应用试验，结果表明：交播技术可用于马尼拉、狗牙根和矮生百慕大等暖季型草坪上，交播时间宜在10月底前进行，交播种子用量多年生黑麦草以20－30g/m^2为宜。     

Comparison of a new gold-immunochromatographic assay for the detection of antibodies against avian influenza virus with hemagglutination inhibition and agar gel immunodiffusion assays

A gold-immunochromatographic test-strip kit is used for the detection of IgG antibodies against the nucleocapsid protein of Avian Influenza Virus (AIV). Compared with the "gold standard", i.e. hemagglutination inhibition (HI) and agar gel immunodiffusion (AGID) assays, the gold-immunochromatographic test strip has many advantages, such as high specificity, high sensitivity, convenience, is rapid and has low cost. The gold-immunochromatographic test strip provides a unique tool for the on-site surveillance and diagnosis of Avian Influenza.     

Comparative development of mouse tooth germs transplanted in subrenal capsule and oral submucosa

AIM: To compare 2 environments, the subrenal capsule and oral submucosa, for producing well-formed teeth from mouse tooth germs and for exploring the ideal environment for tooth regeneration. METHODS: Two groups were set up. Group A was transplanted with the mouse embronic day (ED) 14.5 first mandibular molar tooth germs into the subrenal capsule, while group B was transplanted with the ED14.5 first mandibular molar tooth germs into the oral submucosa. After 3 weeks and 4 weeks, the host mice were sacrificed, and the transplanted explants were evaluated with morphologic observation, histological structures, hardness and elastictic modulus tests, and chemical compositions. RESULTS: (1) The explants isolated from both environments showed the tooth-like structures, but as to the group B, the crown was smaller, and the shape of the cusps was not significant. (2) HE staining showed that the dentin and enamel in group A were thicker than those in group B in which the ameloblasts and odontoblasts were differentiated not very well. (3) In the test of enamel hardness, only the hardness of 4 weeks in group B was lower than normal mouse tooth. In the test of enamel modulus, the elastic modulus of enamel in 3 weeks of group A was slightly lower than normal mouse tooth, but the difference was not significant.The elastic modulus of enamel in 4 weeks of group A and group B was significantly lower than normal mouse tooth and 3 weeks of group B. The hardness and elastic modulus of dentin in 3 groups was not significant. (4) Raman spectroscopy showed 2 groups grew in harmony in general, they all had the largest peak in the point of 961 cm^-1, but the 3 weeks of group B had an obvious peak in the point of 2 947 cm^-1. CONCLUSION: For the development of ED14.5 tooth germs, we obtain almost the whole tooth in subrenal capsule transplantation after 3 or 4 weeks. The buccal submucosa environment still has a certain influence on the tooth germ development, although there are some differences about the tooth development between this environment and subrenal capsule environment.