从2015汉诺威国际农机展浅谈拖拉机发展趋势

结合2015汉诺威国际农机展上呈现出的拖拉机新技术,系统阐述国外拖拉机企业的发展特点,并给出国内拖拉机企业的发展建议。     

中国六省土地沙漠化敏感性时空格局与趋势分析

以我国新疆维吾尔自治区、青海省、内蒙古自治区、甘肃省、宁夏回族自治区和陕西省六省区为研究区,分析了1990年、2000年、2005年、2010年4个时期的土地沙漠化敏感性空间格局分布和时间动态变化特征,探讨变化成因并采用CA-Markov耦合模型对土地沙漠化敏感性格局变化趋势进行预测。结果表明:中国六省四期土地沙漠化敏感性格局相似,各级敏感区按分布面积大小排序为:轻度敏感区域 > 中度敏感区域 > 高度敏感区域 > 不敏感区域 > 极敏感区域。极敏感区域主要分布在土壤质地为流动沙地的沙漠区域,不敏感区域主要分布在高山、湖泊附近;人口增多、人为活动强度增加的区域敏感性程度增高;建立治沙工程的区域敏感性降低。对2020年土地沙漠化敏感性格局预测结果显示,相比2010年,极敏感区域在原有的基础上向外围扩张了7 120.04 km²,增幅为4.63%。本文通过分析中国六省土地沙漠化敏感性时空格局与趋势,为中国土地沙漠化防治分区策略制定和划分沙漠化扩展屏障区提供科学依据。     

罗布麻属和白麻属种子形态特征及生活力的测定方法

以采自新疆维吾尔自治区阿勒泰市阿拉哈克镇境内的罗布麻属(Apocynum)和白麻属(Poacynum) 8个基因型植物的种子为材料,进行了8个基因型植物种子形态特征、千粒重和生活力测定方法探究。研究结果显示,参试罗布麻种子的长为2.75 mm,宽为0.68 mm,厚为0.49 mm。白麻属7个基因型中以紫斑中花的种子最长,为4.51 mm;青杆白花最宽,为0.90 mm;青杆白花和大叶白麻最厚,为0.61 mm。8个基因型种子的长、宽、高的变化范围分别为2.75～4.51、0.68～0.90和0.48～0.61 mm。其中,紫斑中花为最大基因型,罗布麻为最小基因型。千粒重变化范围在0.38～1.32 g,所有参试种子颜色均为褐色,其中以大叶白麻颜色最深。参试种子均表现出非休眠性种子萌发的特征,萌发时间较短,可以用来快速测定参试种子的生活力。采用四唑染色测定生活力时,参试种子均表现出不透四唑的特征,应该纵切切破种皮,预湿时间为12～14 h,染色时间为12 h,鉴定标准为种子胚80%完全染色。此次针对罗布麻属和白麻属种子形态特征与生活力测定方法的研究,能够为罗布麻种子生活力鉴定、大规模种...     

基于SWOT分析的山东省农业旅游研究

采用SWOT分析法分析山东省农业旅游发展中的优势、劣势、机会和威胁,并提出了山东省发展农业旅游的对策和措施。     

核桃芽接育苗技术

研究分析了核桃播种方式，播种方法，播种量，接穗培养,家接时间，剪砧程度，嫁接方法等芽接育苗技术的关键，使田间大面积嫁接成活率可达93％左右。     

层次分次法在人工植被选择上的应用

将人工植被生长所需的条件用层次分析法进行比较和判断,最后做出选择种植何种植物的决策.运用层次分析法针对温度、水分和土壤3个要素建立层次结构模型,构造各项评价指标的判断矩阵,并计算权重.通过定性分析与定量分析相结合的方式来确定待种植物,可以实现植被种植的科学性和合理性.     

原料表面碱液处理对稻草碎料板力学性能的影响

在实验室条件下探索了稻草原料表面碱液处理对稻草碎料板力学性能的影响.试验表明,处理后的稻草碎料板的内结合强度比处理前有大幅度提高,弯曲弹性模量和静曲强度比处理前则有所下降,但都达到了相关的国家标准;2h吸水厚度膨胀率升高,超过国家标准.因此稻草表面碱液处理提高了稻草原料表面润湿性和胶合强度,但对稻草碎料板的力学性能有影响.     

松茸菌株对6种松树幼苗的感染及其菌根解剖学研究

利用我国滇产松茸9924菌株及日产松茸99606菌株，分别对云南松、华山松、马尾松、火炬松、湿地松及加勒比松6种松树幼苗实施人工菌根接种。研究结果表明，接种后90d的云南松和湿地松分别有75％和78．1％的幼苗受感染并形成菌根；接种后180d,6种松树幼苗分部都可形成菌根，菌根感染率分别达90．63％－100％，感染指数达50．00－84．68；菌根形态主要有棒状、二叉分枝状及多叉分枝状3种；随树种的不同，各类菌根形态所占比例也不同；不同树种根系上形成菌根的长度也有差异，以马尾松根系上的菌根最长，华山松的菌根最短；此外，各种组合之间在菌套厚度，哈蒂氏网结构上也略有差别。     

Role of PPARα/PGC-1α in doxorubicin induced mouse dilated cardio-myopathy

AIM: To investigate the changes of peroxisome proliferator-activated receptors (PPAR)α/peroxisome proliferator activated receptor coactivator 1 alpha (PGC-1α) in doxorubicin (DOX) induced dilated cardiomyopathy (DCM) and its effect on the energy metabolism and myocardial function in mice. METHODS: Forty mice were randomly divided into 4 groups: control group, DOX group, PPARα inhibitor group and PPARα agonist group. The DCM model was established by injection of DOX. The protein levels of PPARα/PGC-1α were detected. The PPARα inhibitor and PPARα agonist were used 2 weeks beforeinjection of DOX. The contents of adenine acid and phosphocreatine (Pcr) in the mitochondria were measured by high-performance liquid chromatography (HPLC). The ANT activity was analyzed by the atractyloside-inhibitor stop technique. The changes of the echocardiography and hemodynamics were also observed. RESULTS: DOX induced DCM model was successfully established. The protein levels of PPARα and PGC-1α in control group were significantly higher than those in DOX group (P<0.05). Both of the high-energy phosphate contents and the transport activity of ANT were decreased in DOX group (P<0.05), and the hemodynamic parameters were disordered (P<0.01). Compared with DOX group, PPARα inhibitor pre-treatment significantly reduced the PPARα/PGC-1α expression. Meanwhile, high-energy phosphate contents in the mitochondria and the ANT transport activity of the mitochondria decreased, as well as the left ventricular function (P<0.05). On the other hand, PPARα agonist significantly increased the expression of PPARα and PGC-1α, and improved the transport activity of ANT. In addition, the hemodynamic parameters were ameliorated, but the high-energy phosphate contents of the mitochondria did not significantly change. CONCLUSION: PPARα/PGC-1α plays an important role in the regulation of ANT transport activity in dilated cardiomyopathy induced by DOX, and the activation of PPARα/PGC-1α has protective effects on the DCM induced by DOX.     

Juglone inhibits epithelial-mesenchymal transition of prostate cancer cells by regulating Wnt/β-catenin/Snail signaling pathway

AIM: To investigate the mechanism of juglone on epithelial-mesenchymal transition in prostate cancer cells. METHODS: Human prostate cancer LNCaP cells were divided into control group (without juglone), 12.5 μmol/L juglone group and 25 μmol/L juglone group. LNCaP cells in the latter 2 groups were treated with juglone for 24 h. The invasion ability of the LNCaP cells was detected by Transwell assay. The protein expression of E-cadherin, vimentin, Snail and β-catenin was determined by Western blot. The LNCaP cells were treated with LiCl and juglone in combination for 24 h, and the protein expression of Snail and E-cadherin was detected by Western blot.RESULTS: The results of Trans-well invasion assay showed that the invasion ability in juglone groups was significantly decreased (P<0.01). The protein expression of E-cadherin in the LNCaP cells treated with juglone was increased, and the expression levels of vimentin and β-catenin were reduced (P<0.01). Treatment with LiCl significantly attenuated the inhibitory effect of juglone on Snail expression and subsequent down-regulation of E-cadherin expression. CONCLUSION: Juglone inhibits the epithelial-mesenchymal transition by inhibiting the Wnt/β-catenin/Snail signaling pathway in the LNCaP cells.