259 resultados para 331.8


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本文以黄土高原丘陵区陕北延安燕沟流域为例,研究了退耕地土壤有机碳、全氮和酶活性对植被恢复过程的响应。结果表明,随植被恢复年限的增加,植被盖度、多度和物种数均呈现先增加后减少然后又增加的趋势。同当年对照农地相比,随着植被恢复年限的增加,表层(0~20 cm)土壤有机碳、全氮、蔗糖酶、脲酶和碱性磷酸酶活性均明显增加,过氧化氢酶活性随植被恢复年限的增加变化不明显。同对照农地相比,表层土壤有机碳、全氮、蔗糖酶、脲酶和碱性磷酸酶活性分别增加了35%~184.6%、5.7%~157.4%、89.6%~566%、32.9%~331.2%和0.18%~184.8%。表层土壤有机碳和脲酶活性对植被恢复的响应是在植被恢复初期(0~8年),随植被恢复年限的增加而增加,植被恢复8~29年期间,随植被恢复年限的增加而减少,而植被恢复29 a以后,又随植被恢复年限的增加而增加。而表层土壤全氮、蔗糖酶和碱性磷酸酶活性对植被恢复的响应是在植被恢复初期(0~16年),随植被恢复年限的增加而增加,植被恢复16~29年期间,随植被恢复年限的增加而减少,植被恢复29 a以后,又随植被恢复年限的增加而增加。表层土壤蔗糖酶、脲酶和碱性磷酸酶活性与有机碳...

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针对朱基总理 1 999年 8月 7日讲话精神和旱农技术在特殊的自然条件和社会条件下为了良化农田生态环境和持续增产所采取的一整套用地与养地相结合的技术体系。文章着重的分析了培肥地力、轮作倒茬、化学技术、选育品种、节水、立体种植、地膜覆盖、水土保持耕作法八种技术 ,充分利用光、热、水、气、土、肥资源而取得明显的社会效益、经济效益和生态效益 ,剖析了旱作技术在农业持续、稳定、健康发展中的作用和改善农业生态环境的显著地位 ,供同类地区的决策者和研究者借鉴

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选用硝酸和过氧化氢作为消解剂,采用微波技术消解蛹虫草样品,用电感耦合等离子体发射光谱(ICP-AES)法同时测定其中K、P、Ca、Mg、Cu、Fe、Zn、Mn共8种微量元素的含量。进行微波消解条件的优化选择及分析线性、精密度和回收率等实验,建立同时测定蛹虫草中多种微量元素的微波消解-ICP-AES方法。本方法所测元素的标准曲线均有良好的线性关系,以猪肉粉国家标准物质GBW08522为对照进行验证,其回收率为91%~106%,相对标准偏差(RSD)<3.0%;该法加标回收率为90%~108%,RSD<3.0%,具有较好的准确度和精密度,是一种快速、准确而高效的分析方法。测定结果表明,蛹虫草富含有K、P、Mg、Ca、Zn元素。

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本文对中国东北 8种藓类植物染色体数目进行了报道。其中赤茎藓Pleuroziumschreberi (Brid .)Mitt.,n =5 ;塔藓Hylocomiumsplendens (Hedw .)B .S .G .,n =11;粗肋羽藓Thuidiumrecognitum (Hedw .)Lindb .,n =11;绿羽藓T .assimile (Mitt.)Jaeg .,n =11;四齿藓TetraphispellucidaHedw .,n =8;侧枝匐灯藓Plagiomniummaximoviczii (Lindb .)Kop .,n =6 ;尖叶匐灯藓P .cuspidatum (Hedw .)Kop .,n =12 ;具缘提灯藓Mniummarginatum (With .)Beauv .,n =6。绿羽藓的染色体数目为首次报道 ,赤茎藓 ,塔藓 ,粗肋羽藓和四齿藓为国内首次报道

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掺杂的CeO2基固体电解质因其在中低温条件下(500 ̄700℃)具有高氧离子电导率而成为有希望的IT-SOFCs(intermediate temperature-solid oxide fuel

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The Mg-8.31Gd-1.12Dy-0.38Zr (mass%) alloy was prepared by casting technology, and the microstructure, age hardening behavior and mechanical property have been investigated. It is noted that the alpha-Mg and the different Mg-RE (RE = Gd/Dy) compounds are subsistent in the as-cast and annealed state samples. The age hardening behavior is observed during the investigated temperature range, and the alloy exhibits high Vickers hardness, excellent ultimate tensile strength and yield strength at peak hardness.

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By using the bifunctional ligand, 8-hydroxyquinoline-functionalized organosilane (Q-Si), the new mesoporous material Q-MCM-41 covalently bonded with 8-hydroxyquinoline was synthesized. Through the ligand exchange reaction, the new near-infrared (NIR) luminescent mesoporous LnQ(3)-MCM-41 (Ln = Er, Nd, Yb) materials were prepared by linking the lanthanide quinolinate complexes to the ordered mesoporous Q-MCM-41 material. The LnQ(3)-MCM-41 materials were characterized by powder X-ray diffraction and N-2 adsorption/desorption, and they all show the characteristic mesoporous structure of MCM-41 with highly uniform pore size distributions.

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A novel mesoporous material covalently bonded with 8-hydroxyquinoline (HQ) was synthesized (designated as Q-SBA-15). The 5-formyl-8-hydroxyquinoline grafted to.(3-aminopropyl)triethoxysilane, that is, alkoxysilane modified 8-hydroxyquinoline (Q-Si), was used as one of the precursors for the preparation of the Q-SBA-15 material. On the basis of the other function of the Q-Si of coordinating to lanthanide (Ln) ions, for the first time, the LnQ(3) complexes (Ln = Er, Nd, Yb) have been covalently bonded to the SBA-15 materials.

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A novel cemented carbides (W0.5Al0.5)C-0.8-Co with different cobalt contents were prepared by mechanical alloying and hot-pressing technique. Hot-pressing technique as a common technique was performed to fabricate the bulk bodies of the hard alloys. The novel cemented carbides have superior mechanical properties compared to WC-Co. The density, operating cost of the novel material were much lower than WC-Co. There is almost no eta-phase in the (W0.5Al0.5)C-0.8-Co cemented carbides system although the carbon deficient get the value of 20%, and successfully got the nanostructured rounded (W0.5Al0.5)C-0.8 particles.

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We developed a series of highly efficient blue electroluminescent polymers with dopant-host systems and molecular dispersion features by selecting 1,8-naphthalimide derivatives as the light blue emissive dopant units, choosing polyfluorene as the deep blue emissive polymer host and covalently attaching the dopant units to the side chain of the polymer host. The polymers' EL spectra exhibited both deep blue emission from the polymer host and light blue emission from the dopant units because of the energy transfer and charge trapping from the polymer host to the dopant units.