338 resultados para Mg absorption
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本文综述了草原群落土壤呼吸研究的理论、方法、最新进展和主要成果。从2001年6月5日到10月15日,在内蒙古锡林河流域的一个典型草原群落放牧地段用气相色谱法对土壤呼吸进行了测定,并同期观测相应的环境因子,分析了它们之间的相互关系,并根据根系生物量和土壤呼吸的相关性外推出根系呼吸占土壤总呼吸的比例。同时,采用碱液吸收法对该草原群落和一个沼泽化草甸群落的土壤呼吸进行了比对测定,比较在不同生境下土壤呼吸速率的差异。另外,重点比较了两种常用的土壤呼吸测量方法——碱液吸收法和气相色谱法对典型草原群落土壤呼吸的测量效果。主要研究成果如下: 1.在草原群落,生物量(包括地上和地下生物量)、温度(包括气温和土壤温度)和水分及土壤呼吸的季节变化均呈不规则的波动曲线;土壤呼吸与土壤湿度高度相关,与温度尤其是土壤温度以及地下生物量之间存在着一定的相关性,但和地上生物量及绿色生物量之间几乎没有关系。 2.草原群落和草甸群落土壤呼吸的季节动态基本一致,均出现了两个峰值,分别出现在6月底和7月底,它们的变化范围分别为312.8~1738.9 mg C﹒m-2﹒d-1 和 354.6 ~2235.6 mg C﹒m-2﹒d-1,日平均土壤呼吸速率分别为785.9 mg C﹒m-2﹒d-1 和1349.6 mg C﹒m-2﹒d-1,草甸群落的土壤呼吸速率明显高于草原群落; 3.土壤水分是草原群落土壤呼吸的主要限制因子,但对草甸群落的土壤呼吸变化却基本没有影响;草甸群落中,地上总生物量与土壤呼吸速率间没有显著的相关关系,但地上部分绿色生物量与土壤呼吸间存在着显著的幂函数关系,而在草原群落中,土壤呼吸速率与地上活生物量或地上总生物量的相关关系均很弱。 4.在草原群落,根系呼吸占土壤总呼吸的比例为60.7% - 93.3%,平均为82%; 5.碱液吸收法和气相色谱法的测定结果具有很高的相关性(R2=0.7563),它们的季节动态基本一致,变化范围分别为从249.3~1795.1 mg C﹒m-2﹒d-1和从312.8~1738.9 mg C﹒m-2﹒d-1,平均值分别为634.2 mg C﹒m-2﹒d-1和802.7 mg C﹒m-2﹒d-1,碱液吸收法的测量值是气相色谱法的约1.4倍。
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本论文对草地群落地上/地下生物量构成、根冠比特征及其影响因子以及土壤呼吸测定方法比较等的国内外研究进展和主要成果进行了综述,在此基础之上对地处我国北方农牧交错带中段的内蒙古多伦县境内的18种草地群落(包括天然草地和人工草地群落)进行了相关内容的研究工作。 在2002年生长季期间,对这18个植物群落中选取的16个进行了群落学调查,测定了其地上、地下生物量,同时测定了土壤含水量、土壤容重、土壤全氮含量和土壤有机质含量。分别分析了地上、地下生物量以及根冠比(root to shoot ratio)与这些立地因子间的相关关系。同期,从18个群落中选定10个代表性群落测定其土壤呼吸速率,测定方法选用了动态红外气体分析法 (Infra red gas analysis, abbreviated as IRGA)和碱液吸收法(Alkali absorption, abbreviated as AA)。对这两种方法的测定结果进行了比较分析,同时分析了不同群落间土壤呼吸变化与土壤水分和养分状况等的相关关系。主要结论如下: ①16种植物群落的地上和地下生物量差异明显,地上生物量变化范围在80~500 g•m-2之间;相比之下,地下生物量的变化范围要大得多,16个群落中地下生物量最小的为猪毛菜群落,最大的为拂子茅群落,分别为533 g•m-2和2590 g•m-2。群落的根冠比在1.5~11.21之间,平均根冠比为 5.69。 ②土壤含水量对地上和地下生物量有着重要的影响,土壤含水量高的样地(羊草样地)较含水量低(小米蒿样地)的样地地上生物量高,反之亦然。但含水量与地下生物量之间的这种关系却不明显,即土壤含水量高的样地其地下生物量并不一定比含水量低的样地地下生物量高;根冠比与土壤含水量之间基本上呈负相关。土壤全氮含量和有机质含量与地上、地下生物量也存在着一定的正相关关系,而土壤容重却与生物量存有负相关关系;根冠比与土壤全氮、有机质和容重的关系正好与此相反,即根冠比与全氮和有机质含量呈负相关,与容重为正相关。 ③10种植物群落土壤呼吸的昼夜变化比较明显,均为单峰型曲线,主要受土壤温度的驱动,但同时也受到当日降水情况和云量、风速等气象因子的较大影响。因此,影响到这些群落土壤呼吸日动态的一致性,使得规律性并不明显。 ④用碱液吸收法和动态密闭气室法测定的10个群落的土壤呼吸速率变化范围分别为394~894mg C•m-2•d-1和313~2043 mg C•m-2•d-1,其中碱液吸收法测定结果平均为动态气室法的67.5%,明显低于动态密闭气室法。 ⑤两种测定方法具有很好的相关性,R2为0.8739。本研究中发现,在土壤呼吸速率低的情况下,两种方法的测定结果十分接近,甚至碱液吸收法的测定结果稍大于动态密闭气室法;而在土壤呼吸速率较高的情况下,动态密闭气室法测定结果则显著高于碱液吸收法。上述结果与国内外同类研究的结果高度一致,从而为校正我们以往采用碱液吸收法在该区域的测定结果提供了可靠依据。 ⑥各个群落间的土壤呼吸变化与立地土壤水分和土壤养分之间存有一定的相关关系,但并不显著,可能与这些群落土壤呼吸测定不是在同一天进行有关。
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The use of malachite green (MG) in fish farming is prohibited in China due to its potentially toxicological and carcinogenic nature, but it is still illegally used in some places. Uptake, accumulation and deputation of MG in various tissues were studied under laboratory conditions in three common freshwater fish, Parabramis pekinensis (plant-eating fish), Carassius auratus (omnivorous fish) and Ophiocephalus argus (carnivorous fish). The concentrations of MG and its primary metabolite, the reduced and colorless leucomalachite green (LMG), were analyzed by liquid chromatography-mass spectrometry (LC-MS2). Absorption of MG occurred during the waterborne exposure and the MG concentrations in gills of the three fish species all showed a maximum at 0 h after an acute water exposure (6 mg l(-1) MG for 20 min). Afterwards, both MG and LMG declined very rapidly in the blood of the fish. Levels of MG and LMG were still above 0.002 mu g g(-1) in fresh weight muscle at 240 h and may persist for as long as 10 days. Most MG was converted rapidly to LMG in the fish and deputation of LMG was very slow in fat tissue. skin and gonads of the fish. Distribution of LMG was strongly dependent on the fat content in the tissues of the fish, but not related to their different feeding habits. Therefore, it appears that fat tissue, skin and gonads of the fish contaminated by MG and LMG pose the greatest risk for human consumption. (C) 2008 Published by Elsevier B.V.
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A rapid and sensitive method for separation and determination of Cr(VI) and Cr(III) in bottom mud of lake by flow injection on-line preconcentrtion system and GFAAS was developed. The available Cr(VI) and Cr(III) were extracted by HOAc or EDTA + NH4 NO3 and adsorbed simultaneously by an anion and a cation resin microclummn and then eluted simultaneously by 2 mol/L NH4 NO3 + 0.05 mol/L ascorbate and 2 mol/L H2SO4, respectively. The elution was performed for 50 s after adsorption for 2 min, and the efficiencies of elution were 85.4% - 94.8% and 96.7% - 106% for Cr(VI) and Cr(M) respectively. The detection limits of the method were 0.9 mu g/L and 2.7 mu g/L with relative standard deviations of 3.5% and 6.4% for the determination of Cr(VI) and Cr(III) in sample, respectively.
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In this work, the photodegradation of the carcinogenic pollutant 2-naphthol in aqueous solution containing Aldrich humic acid (HA) and ferric ions (Fe(III)) under 125 W and 250 W high pressure mercury lamp (HPML, lambda >= 365 nm) irradiation was investigated. The photooxidation efficiencies were dependent on the pH values, light intensities and Fe(III)/HA concentration in the water, with higher efficiency at pHs 3-4, and 50 mu mol l(-1) Fe(III) with 20 mg l(-1) HA under 250 W HPML. The initial rate of photooxidation increases with increasing, the initial concentration of 2-naphthol from 10 mu mol l(-1) to 100 mu mol l(-1), while do not change at 50 and 100 mu mol l(-1). However, higher removal efficiency of 2-naphthol is achieved at its lower initial concentration of 10 mu mol l(-1), and initial rate of photooxidation is 0.193 mu mol l(-1) min(-1). Dissolved oxygen (DO) plays an important role in the system containing Fe(III)-HA complexes in which Fenton and photo-Fenton reactions were enhanced in the environment. Hydroxyl radicals produced in HA solution with or without ferric ions were determined by using benzene as free radical scavenger and phenol as scavenging products proportional to hydroxyl radicals. By using UV-Vis and excited fluorescence spectrum techniques, the main photooxidation products, which have higher absorption in the region of 240-340 nm, were found, and the mechanisms for the oxidative degradation is proposed.
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Using the density function theory within the generalized gradient approximation, the band structures of wurtzite ZnO, BeO and MgO have been calculated. The effective-mass parameters are fitted using the calculated eigenvalues. The Dresselhaus spin-orbit effect appears in the k[1 00] direction, and is zero in the high symmetry direction k[00 1]. The orderings of valence band split by the crystal-field and spin-orbit coupling in wurtzite ZnO, BeO and MgO are identified by analyzing the wave function characters calculated by projecting the wave functions onto p-state in the spherical harmonics. For wurtzite ZnO, the ordering of valence band is Still Gamma(7) > Gamma(9) > Gamma(7) due to the negative spin-orbit coupling splitting energy and the positive crystal-field splitting energy. Thus, the Thomas' conclusion is confirmed. For wurtzite BeO and MgO, although their orderings of valence bands are Gamma(7) > Gamma(9) > Gamma(7) too, the origins of their orderings are different from that of wurtzite ZnO. Zn1-x,YxO (Y = Mg, Be) doped with N and P atoms have been studied using first-principles method. The calculated results show that N atom doped in Zn1-x BexO has more shallow acceptor energy level with increasing the concentration of Be atom. (C) 2008 Elsevier B.V. All rights reserved.
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InGaN/GaN multi-quantum-well blue (461 +/- 4 nm) light emitting diodes with higher electroluminescence intensity are obtained by postgrowth thermal annealing at 720 C in O-2-ambient. Based on our first-principle total-energy calculations, we conclude that besides dissociating the Mg-H complex by forming H2O, annealing in O-2 has another positive effect on the activation of acceptor Mg in GaN. Mg can be further activated by the formation of an impurity band above the valence band maximum of host GaN from the passivated Mg-Ga-O-N complex. Our calculated ionization energy for acceptor Mg in the passivated system is about 30 meV shallower than that in pure GaN, in good agreement with previous experimental measurement. Our model can explain that the enhanced electroluminescence intensity of InGaN/GaN MQWs based on Mg-doped p-type GaN is due to a decrease in the ionization energy of Mg acceptor with the presence of oxygen. (C) 2008 American Institute of Physics.
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The hole subband structures and effective masses of tensile strained Si/Si1-yGey quantum wells are calculated by using the 6x6 k.p method. The results show that when the tensile strain is induced in the quantum well, the light-hole state becomes the ground state, and the light hole effective masses in the growth direction are strongly reduced while the in-plane effective masses are considerable. Quantitative calculation of the valence intersubband transition between two light hole states in a 7nm tensile strained Si/Si0.55Ge0.45 quantum well grown on a relaxed Si0.5Ge0.5 (100) substrates shows a large absorption coefficient of 8400 cm(-1).