地中膜冬小麦田的水分平衡和节水效益

地中膜技术是在地下不适当深度铺上同强度、耐久性强的聚氯乙烯薄膜,再将土回填。审较为经济的、易于在沙漠地区大面积推广的新型农业技术。试验表明,在传统栽培措施下,利用地事膜种植的冬小麦与对照区冬小麦的相比;产量提高７３．３％,每年增加收益国２６５５．０２＄／ｈｍ＾２,水分利用效率提高８１．３％。     

N2O production in the organic and mineral horizons of soil had different responses to increasing temperature

Journal of Soils and Sediments - The responses of N2O emission to increasing temperature in different soil horizons are not clearly understood yet. Here, we investigated the effects of increasing...     

山西省冬小麦生产潜力时空分布与气象因子分析

估算一定区域内作物生产潜力,对于明确该区域作物生产力及其限制因子具有重要意义。采用农业生态区域法和生产潜力递减机制法估算山西省冬小麦生产潜力,并解析其与主要气象因子的关系。结果表明,2004-2013年山西省冬小麦平均光合、光温、气候和土地生产潜力分别介于63.63~74.81、10.86~12.97、3.68~5.65和2.71~4.73t/hm ²。山西冬小麦生产潜力分布特征为南部普遍低于中部地区,中部盆地地区普遍低于东西部高海拔地区。与2004-2008年相比,2009-2013年晋中西部地区和吕梁冬小麦光合和光温生产潜力有所增加,而晋中东部和长治东部的冬小麦气候和土地生产潜力有所降低。限制冬小麦气候和土地生产潜力的主要气象因子是生育期降水量和日平均温度。     

夏玉米田作物蒸腾与棵间土壤蒸发模拟计算方法研究

本文依据能量平衡原理和质量守恒定律，提出了作物蒸腾与棵间土壤蒸发的估算模式，并对参数的估算做了详细的分析和讨论。最后利用试验区实测资料，通过田间水热耦合运移的数值模拟，对夏玉米田作物蒸腾棵间土壤蒸发模型及其模拟计算方法进行了验证，结果表明，本文提出的模型和模拟计算方法是有效而实用的。     

纳豆激酶液体发酵条件的优化

利用单因素及正交试验,对纳豆枯草芽孢杆菌(Bacillus subtilis natto)液体发酵生产纳豆激酶(Nattokinase,NK)的培养基组成(碳氮比和离子组成)和培养条件(温度、pH值、发酵时间、接种量和装液量等)对产酶量的影响进行了研究。结果表明,最佳发酵培养基组成及发酵条件分别为:可溶性淀粉2.0%,大豆蛋白胨1.5%,Na2HPO4·12H2O0.4%,KH2PO40.2%,MgSO4·7H2O0.075%,CaCl20.01%,培养温度37℃,pH值7.0,发酵时间24h,转速180r/min,种龄16h,接种量3%,装液量25mL/250mL。在优化发酵条件基础上,进行了5,20L发酵工艺放大的初步研究,在此条件下,摇瓶,5L罐和20L罐发酵酶活最高分别达到915,1086,946IU/mL。     

基于TM遥感影像的森林类型分类方法比较

以吉林省汪清林业局为例,基于Landsat5-TM影像,充分利用遥感影像光谱信息,分别采用动态聚类法和组合监督分类法对该林区的森林类型进行分类,并对分类结果的精度进行比较分析.研究结果表明,利用组合监督分类的精度比动态聚类法分类的精度要高,总体分类精度高11％,其中针叶林、阔叶林、混交林和其他用地的分类精度分别高8％、11％、17％和10％.     

Adenosine A2A receptor agonists inhibit lipopolysaccharide-induced production of tumor necrosis factor-alpha by equine monocytes

Adenosine is an endogenous nucleoside that regulates many physiological processes by activating one or more adenosine receptor subtypes, namely A1, A2A, A2B and A3. The results of previous studies indicate that adenosine analogues inhibit lipopolysaccharide (LPS)-induced production of reactive oxygen species (ROS) by equine neutrophils primarily through activation of A2A receptors. Because peripheral blood monocytes produce cytokines that are responsible for many of the deleterious effects of LPS, the current study was performed to evaluate the effects of an array of novel adenosine receptor agonists on LPS-induced production of tumor necrosis factor-alpha (TNF-alpha), and to assess the selectively of these agonists for equine adenosine A2A over the A1 receptor. Radioligand binding studies performed with equine tissues expressing adenosine A1 and A2A receptor subtypes yielded a rank order of affinity for the equine A2A receptor of ATL307>ATL309 approximately ATL310 approximately ATL313>ATL202 approximately ATL361 approximately ATL376>ATL372>CGS21680>NECA. Co-incubation of equine peripheral blood monocytes with LPS and these agonists resulted in inhibition of TNF-alpha production with a rank order of potency that strongly correlated with their binding affinities for equine adenosine A2A receptors. Results of experiments performed with one of the adenosine receptor agonists (ATL313) and selective adenosine receptor antagonists confirmed that inhibition of LPS-induced production of TNF-alpha occurred via stimulation of A2A receptors. Although incubation of monocytes with IB-MECA, a compound purported to act as an adenosine A3 receptor agonist, reduced LPS-induced TNF-alpha production, this effect of IB-MECA was inhibited by the A2A selective antagonist ZM241385 but not by the A3 receptor antagonist MRS1220. These results indicate that the adenosine receptor subtype responsible for regulation of LPS-induced cytokine production by equine monocytes is the A2A receptor. To address the signal transduction mechanism responsible for the anti-inflammatory effects of ATL313 in equine monocytes, production of cAMP was compared in the presence and absence of either the adenosine A2A receptor antagonist ZM241385 or the adenosine A2B receptor antagonist MRS1706. In the absence of the antagonists, ATL313 increased production of cAMP; ZM241385 inhibited this effect of ATL313, whereas MRS1706 did not. Furthermore, incubation of monocytes with either the stable analogue of cAMP, dibutyryl cAMP, or forskolin, an activator of adenylyl cyclase, also inhibited LPS-induced production of TNF-alpha production by equine monocytes. Collectively, the results of the current study indicate that adenosine analogues inhibit LPS-induced production of TNF-alpha by equine monocytes primarily via activation of adenosine A2A receptors and do so in a cAMP-dependent manner. The results of this study indicate that stable adenosine analogues that are selective for adenosine A2A receptors may be suitable for development as anti-inflammatory drugs in horses.     

Physiological and immunological responses to weaning and transport in the young pig: modulation by administration of porcine somatotropin

To examine the effects of exogenous porcine (p) ST on measures of stress and immune function in weaned pigs with or without transport, pigs (20 +/- 1 d of age) received daily injections of pST (0.5 mg/kg; n = 16) or saline (n = 16) for 5 d. On d 5, a blood sample was collected immediately before injection. At 4 h postinjection, pigs were weighed, sampled for blood, injected with di-nitrophenyl-conjugated keyhole limpet hemocyanin, and weaned. One half of the pigs in each group were transported for 3 h before placement in the nursery. Pigs were weighed, and blood was collected on 1, 7, and 14 d postweaning. Statistical significance was set at P < 0.05. Serum IGF-I concentrations were increased by pST and decreased by weaning, but not affected by transport. The free cortisol index was elevated in all pigs 1 d postweaning, although less in transported versus nontransported pigs. By 7 d postweaning, the free cortisol index returned to prewean values. Serum concentrations of immunoglobulin (Ig) G increased in all pigs by 14 d postweaning, but were not affected by pST or transport. Serum IgM concentrations were elevated at 7 and 14 d postweaning. Before weaning and again 1 d postweaning, pigs treated with pST had greater concentrations of IgM than did control animals. Circulating neutrophils increased in pST-treated pigs 4 h after the final pST injection. Improved immune function in weaned pigs by pST may lead to greater health and growth in a commercial setting.     

蜂花粉抗化学性肝损伤研究进展

近年来研究发现蜂花粉具有显著的保肝功效,国内外学者已对此开展了广泛而深入的研究。本文就蜂花粉及活性成分对化学性肝损伤(四氯化碳肝损伤、酒精性肝损伤、氨基半乳糖诱导肝损伤)的作用效果和作用机理等方面的研究进展进行了综述,并对其研究方向和前景进行展望。     

Treatment of experimental ureteral strictures by endourological ureterotomy and implantation of stents in the porcine animal model

The objective of this study is to evaluate the dilation of the ureter using endoureterotomy and an expanding-sheath double pigtail ureteral stent in the treatment of experimentally induced ureteral strictures in the porcine animal model. This is a new treatment in the ureteral strictures resolution in Veterinary Urology, although it is not a common affection, it usually appears as a consequence of ureteritis and in the iatrogenic female genital surgery. The experimental study is design in three phases: induction of experimental stricture, diagnosis and treatment of the stricture and follow-up. We have used 10 healthy Large White female pigs. The internal ureteral diameter was measured prior to laparoscopic ligature stricture induction using retrograde ureteropyelography (RUPG). Experimental stricture was diagnosed 4 weeks after intervention, using RUPG and ultrasound, and treated by endoureterotomy and subsequent placement of a double pigtail ureteral stent, which was removed 6 weeks later. The study finished 4 weeks later with measurement of ureteral diameters using RPUG and ultrasound evaluation. Except in one case, all ureters displayed permanent dilation of the strictured area for 10 weeks after treatment (6 weeks with ureteral stent and 4 more weeks without stent). Finally, this technique proved to be effective in cases of short-length and short-living ureteral strictures, and represents a viable alternative to conventional surgery in animals.