陕北水蚀风蚀交错区两种生物结皮对土壤饱和导水率的影响

该文以陕北水蚀风蚀交错区普遍发育的地表和地上两种生物结皮为研究对象,分别以3种非生物结皮(无结皮、物理结皮、去除生物结皮)为对照,使用盘式入渗仪测定其饱和导水率。结果表明:与无结皮土壤相比,两种类型生物结皮均可极显著降低土壤饱和导水率;与去除生物结皮土壤相比,两种类型生物结皮对土壤饱和导水率的降低均不显著;与有物理结皮发育的土壤相比,地表生物结皮对土壤饱和导水率的降低不显著,而地上生物结皮对土壤饱和导水率的降低显著。一方面,两种生物结皮对土壤饱和导水率均有明显降低作用,预示生物结皮在降雨活动中可能会增加径流、降低入渗,阻碍研究区水分亏缺条件下的植被恢复和生态与环境建设。另一方面,与不同的对照相比,生物结皮对土壤饱和导水率的影响截然不同,该结论可在一定程度上解释当前有关生物结皮影响土壤水分入渗方面所存在的分歧。

植被恢复过程中土壤养分的变化

在纸坊沟流域不同退耕年限的区域采集表层0~20 cm土样274个,分析了不同植被及其退耕年限下的土壤养分变化规律。结果表明,退耕后林草覆盖下的土壤有机质和全氮含量有所增加,特别是刺槐林地增加幅度较大,全磷含量变化不显著,草地覆盖下土壤的速效氮含量低于农田速效氮含量;土壤有机质、全氮、全磷、硝态氮和铵态氮随退耕年限增加呈现出先减少后增加的趋势;退耕年限与土壤有机质和全氮存在显著的正相关性。

大巴山北坡垂直带土壤特性及系统分类

通过野外考察与室内分析相结合 ,对大巴山北坡不同海拔高度的土壤特性进行研究 ,确定了各剖面的诊断层和诊断特性及其在系统分类中的位置。结果表明大巴山北坡各垂直带土壤在系统分类中可划归 2个土纲的 6个土类 ,系统分类中土壤的分类位置与发生分类位置并不具有简单的一一对应的关系。

原子吸收光谱法测定膜荚黄芪不同器官矿质元素含量

应用混合酸HNO3-HClO4(4∶1)在常压微沸条件下对膜荚黄芪根系及茎叶样品进行消解,采用原子吸收光谱法测定了膜荚黄芪不同器官即根及茎叶中五种人体必需矿质元素K,Fe,Zn,Mn和Cu含量,并对结果进行了统计分析与比较。该方法标准曲线相关系数为0.997 3~0.999 9,加标回收率为92.88%~109.25%,相对标准偏差(RSD,n=5)为0.393 5%~3.175 2%。方法简单,结果可靠。结果显示,膜荚黄芪根及茎叶中5种矿质元素含量顺序均为K>Fe>Zn>Mn>Cu。膜荚黄芪不同器官矿质元素含量不同,根中富含Fe,Zn,Cu元素,根内Fe含量是茎叶的1.54倍。茎叶中也含有丰富的矿质元素,特别是K和Mn元素。茎叶中K含量是根的1.63倍,这与黄芪的药效相符合。试验结果将为研究矿质元素在黄芪植株中的分布以及矿质元素含量与黄芪药效相关性提供理论依据。

沃特和PAM保水剂对土壤水分及马铃薯生长的影响研究

在陕北黄土丘陵沟壑区以不施为对照,开展了浸种、穴施保水剂沃特和PAM对土壤水分和马铃薯生长影响研究。结果表明:沃特、PAM不同处理10~20cm、30~40cm土层土壤含水率在盛花前略高于对照,茎叶衰老后略低于对照。不同处理0~100cm土层土壤水含量苗期略高于对照;花期沃特、PAM穴施用量15和30kg/hm2处理极显著高于对照,沃特、PAM穴施用量60kg/hm2和1.0%浸种处理显著低于对照;收获期不同处理均低于对照。不同处理花期、收获期均表现为沃特、PAM施用量越大,生物量、块茎产量越高,块茎个数越少,最大块茎越大。从播种到花期沃特、PAM穴施用量15和30kg/hm2处理的耗水量显著低于对照,从播种到收获期不同处理的耗水量与对照无显著差异,但花期、收获期不同处理的水分利用率和水分产出率均极显著高于对照。沃特和PAM在马铃薯生产应用中,穴施应以30kg/hm2到45kg/hm2为宜。用1.0%的浓度浸种,可成为沃特和PAM在马铃薯生产中利用的主要方式。

延安黄土丘陵沟壑区山坡防蚀道路技术体系及指标

陕北黄土丘陵沟壑区 ,生态环境脆弱 ,水土流失严重 ,作为环境脆弱带的山坡生产型道路 ,对加剧土壤侵蚀起着重要的作用 ,属等外路。人们并不很重视的山坡生产型道路却与农村生产运输、经济交流密切相关 ,其建设与维护具有重要意义。通过对延安黄土丘陵沟壑区山坡生产型道路侵蚀状况调查及对道路防蚀建设的经验 ,总结了现有山坡道路侵蚀现状、方式、影响因素 ,并从生物、工程两方面初步阐述防蚀措施的配置与设计

土石混合介质饱和导水率的研究

采用恒定水头法对土石混合介质的饱和导水率进行测定,分析不同碎石含量及碎石直径对饱和导水率的影响,同时利用实测值对Peck-W atson及Bouw er-R ice两个传统估算方程的估测精度进行比较。结果表明:(1)饱和导水率随碎石含量先增大后减小,且两者呈二项式关系;(2)饱和导水率随碎石直径增大而减小,两者呈幂函数关系;(3)碎石直径介于1.0~5.0 cm时,Bouw er-R ice和Peck-W atson方程对饱和导水率的估算结果均大于实测值。

Nitrogen-15 signals of leaf-litter-soil continuum as a possible indicator of ecosystem nitrogen saturation by forest succession and N loads

National Key Research and Development Program [2010CB833502]; National Natural Science Foundation of China [30600071, 40601097, 30590381]; Chinese Academy of Sciences [KZCX2-YW-432, O7V70080SZ, LENOM07LS-01]; GUCAS [O85101PM03]

Effects of multiple environmental factors on CO2 emission and CH4 uptake from old-growth forest soils

National Key Research and Development Program [2010CB833502]; National Natural Science Foundation of China [30600071, 40601097, 30590381, 30721140307]; Knowledge Innovation Project of the Chinese Academy of Sciences [KZCX2-YW-432, O7V70080SZ, LENOM07LS-01

电化学方法检测DNA碳纳米管修饰电极

在碳纳米管(CNTs)修饰玻碳(GC)后得到CNTs/GC电极的基础上,分别用吸附法和共价键合法制备了脱氧核糖核酸(DNA)修饰的CNTs/GC电极。以硫堇(Th)为电化学指示剂,用循环伏安、示差脉冲伏安、交流阻抗法等测试技术对制备的修饰电极进行了电化学表征。结果表明,用共价键合法制备的DNA修饰的CNTs电极上DNA的固定量多、稳定性好。制备的DNA修饰电极可用于电化学基因传感器等领域。

Carbon-supported Pd–Ir catalyst as anodic catalyst in direct formic acid fuel cell

It was reported for the first time that the electrocatalytic activity of the Carbon-supported Pd-Ir (Pd-Ir/C) catalyst with the suitable atomic ratio of Pd and Ir for the oxidation of formic acid in the direct formic acid fuel cell (DFAFC) is better than that of the Carbon-supported Pd (Pd/C) catalyst, although Ir has no electrocatalytic activity for the oxidation of formic acid. The potential of the anodic peak of formic acid at the Pd-Ir/C catalyst electrode with the atomic ratio of Pd and Ir = 5:1 is 50 mV more negative than that and the peak current density is 13% higher than that at the Pd/C catalyst electrode.

类肝素化合物的傅立叶变换离子回旋共振-电喷雾质谱研究

采用负离子模式的电喷雾傅立叶变换离子回旋共振质谱(ESI-FTICR-MS)对3个合成的肝素类化合物DHα、THα和THβ进行了全扫描一级谱和持续非共振辐照碰撞诱导解离(SORI-CID)串联质谱分析。样品浓度10μmol/L,流动泵注射直接进样。化合物中的磺酸胺和磺酸酯结构容易在一般电喷雾条件下发生分解,失去一个或者多个SO3,一级全扫描谱图中得到的谱峰均是带有单电荷或者双电荷的准分子离子峰。

Platinum-macrocycle co-catalysts for electro-oxidation of formic acid

In this paper, it was found that the electrocatalytic activity of a Pt electrode for the electro-oxidation of formic acid could be dramatically enhanced with the modification of macrocycle compounds, such as iron-tetrasulfophthalocyanine (FeTSPc). The electro-oxidation of formic acid on a modified Pt electrode with FeTSPc occurs mainly through a direct pathway. A series of macrocycle compounds were also investigated as modifiers and exhibited a promotion effect similar to the Pt electrode.

Preparation of Pd/C catalyst for formic acid oxidation using a novel colloid method

A novel colloid method using (WO3)(n)center dot xH(2)O as colloidal source was developed to prepare Pd/C catalyst for formic acid oxidation. Transmission electron microscopy image shows that the Pd/C nanoparticles have an average size of 3.3 nm and a narrow size distribution. Electrochemical measurements indicate that the Pd/C catalyst exhibits significantly high electrochemical active surface area and high catalytic activity with good stability for formic acid oxidation compared with that prepared by common method.