不同贮藏年限老芒麦种胚线粒体抗氧化功能的变化规律

种子在自然贮藏过程中常常伴随着内部生理机能的恶化，线粒体作为种子内活性氧（reactive oxide species，ROS）产生的主要位点是最先遭到破坏的细胞器。为探讨不同贮藏年限对老芒麦种胚线粒体抗氧化功能的影响，本试验以室温贮藏0～4年的老芒麦种子为材料，分析比较其老化规律及种胚线粒体抗氧化特性的变化规律。结果表明：随着贮藏年限的延长，老芒麦种子发芽势、发芽率和种苗鲜重逐渐下降，死种子逐渐增多，种胚线粒体苹果酸脱氢酶（mitochondria malate dehydrogenase，MDH）、谷胱甘肽还原酶（glutathione reductase，GR）、单脱氢抗坏血酸还原酶（monodehydroascorbate reductase，MDHAR）活性逐渐下降，但在死种子中超氧化物歧化酶（superoxide dismutase，SOD）活性显著升高。此外，在贮藏过程中老芒麦种胚线粒体O₂^·-产生速率不断上升，而H₂O₂含量则呈现逐渐降低的趋势，表明线粒体中O₂^·-的积累与细胞氧化损伤密切相关。     

枣品种选择试验研究

1997～1999年对收集引进的22个枣品种进行生长和结果情况调查及物候期定点预测，以大荔圆枣为对照，从丰产性、品质、抗性（抗裂果）、单果重、结果整齐度5个方面进行综合评比，筛选出适宜我省发展的不同用途的枣树优良品种12个，为黄土高原红枣产业化发展提供了品种依据。     

关于我国海水网箱养鱼发展现状与危机分析及可持续发展的探讨

我国海水网箱养鱼发展现状是以个体联合体生产经营为主体的低技术水平的数量规模化，众多传统港湾已形成了大范围的严重超负荷养殖状态，其对环境巨大的污染力引发鱼病猖獗和频受赤潮侵袭，已面临严峻的养殖环境危机。本文综合分析了我国海水网箱养鱼的发展现状与负面效应及其现状危机，并初步进行了危机根源和可持续发展的讨论分析。     

High frequency embryogenic callus induction and plant regeneration from mature caryposis of big bluestem and little bluestem

Big bluestem (Andropogon gerardii Vitman) and little bluestem [Schizachyrium scoparium (Michaux) Nash.] are native to the North America and are important forage grasses and ornamental grasses. Both grasses are proposed as ideal biomass producers for cellulosic ethanol production. To apply genetic transformation, which is an important tool for incorporating desirable agronomic traits into plants to both species, however requires an efficient and reproducible regeneration protocol. We used mature caryopses from big and little bluestem as explants and tested the effect of various combinations of 2, 4-dichlorophenoxyacetic acid (2, 4-D) (1, 2, 3, 4 or 5 mg l⁻¹) and kinetin (KT) (0, 0.1 or 0.2 mg l⁻¹) on embryogenic callus induction with LS as the basal medium. The highest percentage of embryogenic calli induction occurred on medium containing 2, 4-D alone at 2 mg l⁻¹ for ‘Bison’ and on medium containing 4 mg l⁻¹ 2, 4-D alone for ‘Bonilla’ big bluestem. For little bluestem, the highest percentage of embryogenic callus induction occurred on medium containing 3 mg l⁻¹ 2, 4-D plus 0.1 mg l⁻¹ kinetin, suggesting that addition of KT is beneficial. Shoot regeneration took place on LS basal medium without any plant growth regulator for both species, although the addition of KT increased both regeneration frequency and the number of shoots produced per callus. Rooting of shoots reaching about 2 cm long occurred readily with or without α-naphthaleneacetic acid (NAA). Rooted plantlets were all successfully established in the soil.     

落叶松人工林地位指数级导向曲线模型的研究

本文用约1000块样地资抖,系统地研究了黑龙江省落叶松人工林的地位指数级导向曲线模型。通过林业统计分析软件Statistica6.0对各落叶松人工林数据进行拟合、分析比较,结果为：从拟合精度、曲线走向与散点分布趋势、残差分布等综合考虑,舒马切尔曲线函数比较适合落叶松人工林地位指数级导向曲线模型的拟合。     

欧盟共同农业政策面临的挑战及最新改革措施

共同农业政策作为联系欧盟成员国农业的纽带,在经历2003年的改革后,虽然在价格补贴、农村发展等方面取得一定的成效,但仍然面临财政负担、食品安全、新成员国加入等来自内外部的挑战和压力.为应对这些挑战和压力,欧盟进行了降低政策价格、微调配额等一系列的最新改革.     

分散松香施胶剂性能影响因素的探讨

对逆转法制备分散松香施胶剂过程中的主要因素如乳化剂的种类及用量、马来松香加合物含量、搅拌转速、加料速度和乳化温度等系统地进行了探讨，提出了合理的工艺条件，并对实际生产中可能出现的问题及解决办法进行了阐述。     

马传贫驴白细胞弱毒疫苗株跨膜蛋白主要免疫决定区基因的克隆与表达

从感染驴白细胞的马传贫驴白细胞弱毒疫苗株前病毒DNA中克隆了编码跨膜蛋白主要免疫决定区(TMIR)的基因，并在大肠杆菌中进行了表达。所表达的融合蛋白有一部分是可溶的，其氨基端带有6个组氨酸的标签，因此可以用固定化金属离子亲和层析法在非变性条件下进行纯化。在间接酶联免疫吸附试验(ELISA)和免疫印迹试验中，重组的TMIR蛋白可与马传贫阳性血清样品发生反应，而与健康马血清无任何反应。这表明该重组蛋白具有良好的抗原性和特异性，可用于马传贫弱毒疫苗株在体内外复制、接种马体内免疫应答及马传贫诊断的研究。     

羔羊全营养代乳粉对羔羊增重影响的试验

为了研究羔羊出生后采取人工饲喂代乳粉溶液的效果，对10日龄羔羊称重，以平均日增重与母乳组比较，用t检验方法检验差异显著性。研究结果显示羔羊平均日增重试验组为0.097-0.126kg，母乳组为0.071-0.113kg，二者没有显著差异。在生产中，代乳粉能替代绵羊母乳饲喂羔羊，对多胎品系羊的推广应用以及解决绵羊缺乳、少乳或无乳问题具有重要意义。     

Influence of all-trans retinoic acid on proliferation and differentiation of neural stem cells from new born rat striatum

AIM: To study the effect and mechanism of all-trans retinoic acid (atRA) on neural stem cell (NSCs) proliferation and differentiation from new born Sprague-Dawley rat striatum. METHODS: NSCs were isolated from the brains of new born Sprague-Dawley rat striatum, and the features of cells were characterized by immunofluorescence staining. The effects of different culture medium on cell cycle distribution and proliferation of NSCs were determined by flow cytometry (FCM). The effects of atRA on differentiation of NSCs were determined by immunofluorescence staining and classified count of differentiated cells. RESULTS: FCM assay indicated that atRA inhibited the proliferation of NSCs. The percentage of cells in G0/G1 phase in atRA treatment group was significantly higher than that in control, and the proliferation index (PI) was significantly low. The percentage of neurons differentiated from NSCs in atRA group was 2.5 times of the control group after induced by adding 10% FCS in culture medium. CONCLUSION: atRA counteracts the effects of bFGF on the promotion of mitosis and inhibition of differentiation of NSCs. atRA also promotes NSCs to differentiate into neurons in vitro.