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101.
Glucose-6-phosphate dehydrogenase (G6PDH, EC 1.1.1.49) is the first and main regulated enzyme of oxidative pentose phosphate pathway (OPPP), catalyzing the conversion of glucose-6-phosphate to 6-phospho-gluconolactone and playing important roles in the growth and development of plants. It is preciously reported that the enhancement of freezing resistance of Populus suaveolens cuttings is clear related to the distinct increase in cytosolic G6PDH activity. Here, a 1697 bp cDNA fragment (PsG6PDH) is amplified by RT-PCR from cold-induced total RNA of the freezing-tolerant P. suaveolens . A sequence analysis showed that PsG6PDH coding region had 1 530 bp and encoded 510 predicted amino acid residues. Genomic Southern analysis revealed that the isoform is encoded by a few copies of the gene in the poplar genome. The cloned gene PsG6PDH is cloned into binary vector pBI121 and used to transform tobacco. PCR and Southern blotting results verified integration of this gene into the genome of tobacco. Moreover, cold treatment experiments and membrane defense enzyme activity analysis confirmed that overexpression of the PsG6PDH gene could enhance the tolerance to cold or frigid stresses in transgenic plants.  相似文献   
102.
含钙铝铁水解聚合产物的矿物学研究Ⅱ:热分解特性   总被引:2,自引:2,他引:0  
分别以NaOH和Ca(OH)2作为碱化剂,合成了聚合氯化铝铁(PAFCNa,PAFCCa),比较样聚合氯化铝(PACNa,PACCa)、聚合氯化铁(PFCNa,PFCCa),制成低温干燥样进行热分解检测.热重分析证明,PAFCCa中的含水量高,主要是配位水与结晶水.当n(Al)/n(Fe)>5:5后,PAFCCa的含水量平均为42.3%.按Ca6Al2(SO4)3(OH)12·26H2O分子式计算,钙矾石的结构水(含OH水)含量为43.06%,两者含水量相当接近.TG-DTG热分析结果支持XRD对PAFCCa中存在含Ca3Al2(OH)12柱体的类钙矾石结构体的认定.PAFC-Ca根据其DTG曲线上的125℃和180℃两个脱水速率(肩)峰可以判别其中有无钙矾石结构体,以及相对量的多少.  相似文献   
103.
通过对鄂尔多斯盆地延长组长6期湖盆中部地区物源分析、沉积相特征等研究,分析了厚层砂体的形成机理和砂体类型。认为长6期物源主要来自东北、西南方向,发育三角洲前缘水下分流河道、河口坝、远端砂坝和浊流等砂体类型,湖盆演化从鼎盛转向萎缩的长6早期厚层砂体比较发育。白豹、合水地区砂层厚度大,储层条件良好,是石油勘探的有利地区。  相似文献   
104.
SF6气体的辐射强迫和全球增温潜能的研究   总被引:1,自引:0,他引:1  
吴金秀  肖稳安  张华 《大气科学》2009,33(4):825-834
IPCC(2007)指出, 六氟化硫(SF6) 作为臭氧消耗物质 (ODSs) 的部分替代物质, 近年来排放量大大增加。它作为控制排放的人造长寿命温室气体之一已经被列入《京都议定书》。但是, 目前在臭氧消耗物质替代品中, 对SF6的辐射强迫和全球增温潜能的研究较少, 而且所用的谱吸收资料陈旧。本文采用最新的分子吸收数据库HITRAN2004中的SF6的吸收截面数据, 利用Shi(1981) 的吸收系数重排法, 建立了SF6的相关k分布的辐射计算方案, 在此基础上研究了SF6在晴空大气下的辐射效率和全球增温潜能, 并首次计算了SF6的全球温变潜能, 与其全球增温潜能进行了比较。本文的研究表明: SF6的辐射效率为0.512 W/m2, 经过大气寿命调整之后的辐射效率为0.506 W/m2, 二者差别不大; 根据IPCC (2007) 给出的排放情景, 到2100年, SF6在大气中的体积分数将达到35×10-12~70×10-12, 引起的相应辐射强迫将在0.004~0.028 W/m2之间变化; 相对于二氧化碳的100年全球增温潜能为2.33×104, 比IPCC(2007)的结果大2.2%; 100年的持续排放的全球增温潜能为2.26×104, 与其他长寿命人造温室气体一道, 其对全球变暖的长期影响不容忽视。  相似文献   
105.
2008-11-10青海大柴旦地区发生了Mw6.3级地震,其发震断层位于青藏高原东北缘的大柴旦一宗务隆山断裂带。利用欧空局Envisat/ASAR卫星雷达影像数据,采用二通差分干涉技术获得了地震的同震地表形变场,基于1D协方差函数估计InSAR同震形变场的中误差为0.52cm,方差一协方差衰减距离为5.9km。在此基础上,采用弹性半空间矩形位错模型进行断层几何参数反演,并利用断层自动剖分技术确定了地震的最佳同震滑动分布模型。结果表明,该地震的震源机制解为走向107.19°,倾角56.57°,以逆冲为主兼具少量右旋走滑分量;滑动分布主要发生在10-20km深度范围内,最大滑动量为0.51m,释放的能量为4.3×10^18Nm。  相似文献   
106.
A new experimental calibration was undertaken in this study to get a more reliable sphalerite-galena sulfur isotope geothermometer. The experimental conditions selected in study were very similar to those of natural hydrothermal solution. The high-precision SF6 method was used in sulfur isotope analyses. The obtained calibration curve for sulfur isotope fractionation between sphalerite and galena can be expressed with the equation 10001nαSp-Gn= 0.74×106T-2+0.08.  相似文献   
107.
在碱性介质中,痕量Ag(Ⅰ)对新试剂6-(2-羟基-4-二乙基氨苯偶氮)-2,3-二氢-1,4-酞嗪二酮(简称HDEA)的电化学发光具有显著的催化作用。基于此,提出了HDEA-KCI-KOH体系测定矿样中痕量Ag的新方法。方法的检测限为2.0×10~(-8)mol/L Ag,线性范围为5.0×10~(-8)—3.0×10~(-6)mol/L Ag。采用巯基棉富集分离,应用本法测定一些矿样中的Ag,结果良好。  相似文献   
108.
Clinopyroxenes from pyroxenite, ijolite and nepheline syenite from the main intrusion of the Alnö complex define two sub-parallel compositional trends with respect to Na, Ca and FeTOT plotted against alkali-pyroxene fractionation index (Na–Mg). Both trends define a smooth fractionation of increasing Na and FeTOT and decreasing Ca with increasing Na–Mg, but one set of samples contain clinopyroxenes that constantly plot at higher Na and lower FeTOT and Ca (at similar Na–Mg) than the rest of the samples. Clinopyroxenes with higher Ca and FeTOT and lower Na (trend 1) co-exist with substantial amounts of Ti-andradite (up to 70 vol.%), while the sample set defining the more Na-rich trend (trend 2) lack co-existing Ti-andradite. Clinopyroxenes from both trends show fractionated REE patterns with a distinct difference in HREE content, reflecting the content of co-existing Ti-andradite. The rocks of the first Ti-andradite-bearing trend crystallized slightly prior to the rocks of the second trend, probably from a primitive, Ca- and Ti-rich nephelinitic magma. Crystallisation of pyroxenite and melteigite occurred under low aSiO2 and high aCaO and aTiO2 as evidenced by the presence of perovskite and sometimes substantial amounts of magnetite. Subsequent increase in aSiO2 is evidenced in the overgrowth of perovskite by titanite, which in turn is overgrown by Ti-andradite. Nepheline syenitic residuals crystallized under higher aSiO2 and aNa2O and lower aCaO and aTiO2, which reduced Ti-andradite into an accessory phase and produced more Si- and Na-rich clinopyroxenes. Some of these residuals probably also mixed with new primitive magma producing a hybrid magma that crystallised the more Na-rich and Ca- and FeTOT-poor clinopyroxenes of trend 2. The complete lack of Ti-andradite in these rocks indicates different crystallisation conditions and also a different magma composition.  相似文献   
109.
110.
The Mössbauer spectra of natural megacrystal clinopyroxene are usually fitted by 4 sets of symmetric doublets, A‐A', B‐B', C‐C' and D‐D', respectively, in terms of increasing Qs value in literature. But the assignments of those doublets are quite different, except the D‐D' doublet assigned to Fe3+at the lattice site M***1 in previous papers. Particularly, the assignment and interpretation of the C‐C' doublet are diverse. The oxidation experiments of natural megacrystal clinopyroxene collected from the Hannuoba basalt, North China, were performed under controlled conditions of temperature at 1000°C and oxygen fugacity of FMQ buffer in 1, 2, ***3 and 5 days respectively. The oxidized samples were then measured by X‐ray diffraction spectrometry and Mössbauer spectrometry. The oxidation of clinopyroxene is characterized by Fe2+ → Fe3+at M1 under the subsolidus conditions, which is consistent with the increase of the area of the D‐D' doublet when the heating time increases. Accordingly, the area of the A‐A' and B‐B' doublets decreases with the increasing heating time. However, the area of C‐C' keeps almost constant. Therefore, the 4 sets of doublets can be assigned correctly as follows: A‐A' doublet to Fe+2at M1, B‐B' Fe2+at M1, C‐C' Fe2+at M2, and D‐D' Fe3+at M1. The M1 site splitting is due to the NNN (Next Nearest Neighbour) effect of the M2 site. The amount of Fe3+at the tetrohedral site of megacrystal clinopyroxene is negligible according to this study.  相似文献   
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