青海海北高寒湿地近地层大气CO_2浓度的变化特征

采用快速响应红外气体分析仪对青海海北高寒湿地大气CO_2浓度进行连续监测,分析2004年CO_2浓度变化特征表明,CO_2浓度存在明显的日、季变化,日、年内均表现"U"型变化特征.这些变化与植被生理活动、土壤呼吸、大气逆温层、及湍流交换强度等有关.自1月到7月CO_2浓度的日变化过程中,日最高值出现时间在日出前后的5:00到9:00,并随7月的到来逐渐提早,日出后下降,约在下午15:00左右为最低,日落后又逐步升高.7月以后日最高值出现时间随时间推移又滞后,最低提早.一年中,月平均浓度最低值出现在7月份,最高值则在10月.观测表明,2004年海北高寒湿地CO_2年平均浓度为315.3μmol/mol,月平均最高为335.0μmol/mol(10月),月平均最低值为270.1μmol/mol(7月).统计海北高寒湿地旬平均CO2浓度与气象因素线性相关关系表明,海北高寒湿地CO_2浓度与大多数气象因子有显著的负相关关系,但与土壤温度、气压、相对湿度等的相关关系不明显.

青海野生抱茎獐牙菜中矿物质元素含量特征

为了对比分析青海不同地区野生抱茎獐牙菜中微量元素含量，采集花期抱茎獐牙菜全植株，采用原子吸收光谱仪分析了其铜、锌、铁、锰、钴、镍等元素含量。结果表明。不同地区野生抱茎獐牙菜中微量元素含量的变化可能与采样时间有关。

高寒草甸植物地上生物量生长过程的某些特征

分析了高寒草甸植物地上生物量对积温变化的响应。结果表明, 生物量干物质积累(GW ) 与积温(ΣT ) 成明显的正相关关系, 可用逻辑斯谛(Logistic) 曲线方程: GW = 428.5061/〔1+ exp (2. 6076- 0. 0038ΣT ) 〕来描述。通过模拟方程可知, 在日平均气温稳定通过≥0℃积温达678℃·d 左右时地上生物量增长速率最高; 积温在335～ 1020℃·d 之间为生物量平均增长率积累最快的时段。在降水条件适宜的状况下, 未来牧草生长期内气温升高1℃, 高寒草甸植物年产量将有所提高。

Analysis of primary aromatic amines using precolumn derivatization by HPLC fluorescence detection and online MS identification

2-(2-Phenyl-1H-phenanthro-[9,10-d]imidazole-1-yl)-acetic acid (PPIA) and 2-(9-acridone)-acetic acid (AAA), two novel precolumn fluorescent derivatization reagents, have been developed and compared for analysis of primary aromatic amines by high performance liquid chromatographic fluorescence detection coupled with online mass spectrometric identification. PPIA and AAA react rapidly and smoothly with the aromatic amines on the basis of a condensation reaction using 1-ethyl-3-(3dimethylaminopropyl)-carbodiimide (EDC) as dehydrating catalyst to form stable derivatives with emission wavelengths at 380 and 440 nm, respectively. Taking six primary aromatic amines (aniline, 2-methylaniline, 2-methoxyaniline, 4-methylaniline, 4-chloroaniline, and 4-bromoaniline) as testing compounds, derivatization conditions such as coupling reagent, basic catalyst, reaction temperature and time, reaction solvent, and fluorescent labeling reagent concentration have also been investigated. With the better PPIA method, chromatographic separation of derivatized aromatic amines exhibited a good baseline resolution on an RP column. At the same time, by online mass spectrometric identification with atmospheric pressure chemical ionization (APCI) source in positive ion mode, the PPIA-labeled derivatives were characterized by easy-to-interpret mass spectra due to the prominent protonated molecular ion m/z [M + H](+) and specific fragment ions (MS/MS) m/z 335 and 295. The linear range is 24.41 fmol-200.0 pmol with correlation coefficients in the range of 0.9996-0.9999, and detection limits of PPIA-labeled aromatic amines are 0.12-0.21 nmol/L (S/N = 3). Method repeatability, precision, and recovery were evaluated and the results were excellent for the efficient HPLC analysis. The most important argument, however, was the high sensitivity and ease-of-handling of the PPIA method. Preliminary experiments with wastewater samples collected from the waterspout of a paper mill and its nearby soil where pollution with aromatic amines may be expected show that the method is highly validated with little interference in the chromatogram.

新疆萨吾尔金矿带构造-流体地球化学及成矿作用

The Sawuer gold belt is located in the transition belt between Siberian plate and Kazakhstan-Junggar plate. Based on the geological and geochemical studies on the Kuoerzhenkuola and Buerkesidai gold deposits, in Sawuer gold mineralization belt, the time-space structure of mineralization and mineralizing factor are studied, the metallogenic regularity is concluded in thistheses. The ore bodies have the regularity that orebody are of the extensive and compressive in the sallow and depth of volcanic apparatue, respectively, and the vertical extension of orebody is more intensive than the horizontal extension. The gold deposits were controlled by the fractures of volcanic apparatus and regional faults, and featured by the hydrothermal alteration and metasomatism type disseminated mineralization and filling type vein mineralization. By virtue of the geological and geochemical studies on the two deposits that the formation of the two deposits are significantly related to the volcanic activity, we propose new ideas about their origin: (1) the two deposits are located in the same strata, and share the same genesis. (2) both of two deposits are volcanogenic late-stage hydrothermal gold deposits. Based on mapping of volcanic lithofacies and structure for the first time, it is discovered that a volcanic apparatus existed in the study area. Volcanic-intrusive activity can be divided into three cycles and nine lithofacies. where the two deposits are hosted in the same volcanic cycle, in this case, the wall-rock should belong to the same strata. The 40Ar-39Ar age method is employed in this work to analyze the fluid inclusions of quartz in the ore bodies from Kuoerzhenkuola and Buerkesidai gold deposits. The results show that the main mineralization occurred in 332.05 + 2.02-332.59 + 0.5IMa and 335.53 + 0.32Ma~336.78 + 0.50Ma for Kuoerzhenkuola and Buerkesidai gold deposits respectively, indicating that the two deposits are formed almost at the same time, and the metallogenic epoch of the tow deposits are close to those of the hosting rocks formed by volcanic activity of Sawuer gold belt. This geochronological study supplies new evidence for determining the timing of gold mineralization, the geneses of gold deposits? and identifies that in Hercynian period, the Altai developed tectonic-magmatic-hydrothermal mineralization of Early Carboniferous period, except known two metallogenic mineralization periods including tectonic-magmatic-hydrothermal mineralization of Devonian period and Late Carboniferous-Permian period respectively. The study of fluid inclusions indicates that the ore-forming fluid is a type of NaCl-HbO fluid with medium-low temperature and low salinity, Au is transported by the type of auric-sulfur complex (Au (HS)2-), the ore is formed in reduction condition. Hydrogen and oxygen isotopes of fluid inclusions in the major mineralizating stage show that the solutions mainly originated from magmatic water and meteoric water. The fluid mixing and water-rock reaction cause the deposition of Au. The helium and argon isotope compositions of fluid inclusions hosted in pyrite have been measured from Kuoerzhenkuola and Buerkesidai gold deposits in Sawuer gold belt. The results show that the ore-forming fluids of two deposits possessed the same source and is a mixture of mantle- and partial meteoric water-derived fluid, and the reliability of He and Ar isotopic compositions in Hercynian period is discussed. Isotopic studies including H, O, He, C, S, Pb and Sr reveal the same result that the ore-forming fluids of two deposits possessed the same source: the water derived mainly from magmatic water, partially from meteoric water; the mineralizers and ore materials derived mainly from mantle beneath the island arc, and partially from crust. The ore-forming fluids of two deposits are a mixture of mantle-derived fluids being incorporated by crust-derived fluid, and shallow partial meteoric water. Based on these results, it is proposed that the geneses of the two gold deposits are the same, being volcanogenic late-stage hydrothermal gold deposits that the ore-forming fluids filled in fractures of volcanic apparatus and metasomatized the host rocks in the volcanic apparatus. It is the first time we carried out the geophysical exploration, that is, the EH-4 continuous electrical conductivity image system measurement, the results show that relative large-size mineralizing anomalies in underground have been discovered.lt can confirm the law and genesis of the deposits mentioned above, and change the two abandoned mines to current large-size potenial exploration target.

菲在土壤／沉积物上的吸附-解吸过程及滞后现象的研究

实验研究了菲在土壤／沉积物上的吸附一解吸过程。CHL土壤和HFH沉积物中有机质的固相^13C CP MAS NMR谱图很相似，表明样品中有机质的组成差异不大；菲在土壤／沉积物上的吸附过程表现出明显的非线性；线性模型不适合拟合菲的吸附等温线，Freundlich模型和双区位反应模型(DRDM)较好地拟合了菲的吸附等温线，其中DRDM模型还清楚地反映菲在低浓度和高浓度下不同的吸附方式；另外，研究表明菲在土壤／沉积物上的解吸过程中存在明显的滞后现象，这可能和土壤／沉积物有机质的异质性和土壤胶团微小孔隙的存在有关。实验研究了菲在土壤／沉积物上的吸附一解吸过程。CHL土壤和HFH沉积物中有机质的固相^13C CP MAS NMR谱图很相似，表明样品中有机质的组成差异不大；菲在土壤／沉积物上的吸附过程表现出明显的非线性；线性模型不适合拟合菲的吸附等温线，Freundlich模型和双区位反应模型(DRDM)较好地拟合了菲的吸附等温线，其中DRDM模型还清楚地反映菲在低浓度和高浓度下不同的吸附方式；另外，研究表明菲在土壤／沉积物上的解吸过程中存在明显的滞后现象，这可能和土壤／沉积物有机质的异质性和土壤胶团微小孔隙的存在有关。

秦岭造山带泥盆纪三级构造热水沉积成矿盆地主控因素－－大型－－超大型矿床集中区研究（I）

从系统学和协同学角度研究分析了秦岭造山带泥盆纪三级构造热水沉积成矿盆地的主控因素。认为三级构造热水沉积成矿盆地是受诸多因素控制的一个构造--热水成岩成矿系统（一种非线性、自组织系统）。秦岭深部岩石圈地幔近南北向收缩与佛坪大陆热点构造（hotspot）的耦合，引发陆壳浅部发生近东西向伸展，触发热水（能）从深部向陆壳浅部大规模运移。近东西向高序次同生断裂控制一级沉积盆地的形成与演化。不同级次的同生断裂是控盆-成盆的主控因素，低序次NE向、NW向和SN向同生断裂是秦岭造山带泥盆纪三级构造热水沉积成矿盆地的主控因素，也是热水喷流进入盆地的构造通道。三级构造沉积盆地为热水成岩成矿系统发生大规模聚集成矿提供了构造空间。

Simple derivatization method for sensitive determination of fatty acids with fluorescence detection by high-performance liquid chromatography using 9-(2-hydroxyethyl)-carbazole as derivatization reagent

A simple and sensitive method for the determination of short and long-chain fatty acids using high-performance liquid chromatography with fluorimetric detection has been developed. The fatty acids were derivatized to their corresponding esters with 9-(2-hydroxyethyl)-carbazole (HEC) in acetonitrile at 60 degreesC with 1-ethyl-3-(3-dimethylaminopropyl)carbodiimide hydrochloride as a coupling agent in the presence of 4-dimethylaminopyridine (DMAP). A mixture of esters of C-1-C-20 fatty acids was completely separated within 38 min in conjunction with a gradient elution on a reversed-phase C-18 column. The maximum fluorescence emission for the derivatized fatty acids is at 365 nm (lambda (ex) 335 nm). Studies on derivatization conditions indicate that fatty acids react proceeded rapidly and smoothly with HEC in the presence of EDC and DMAP in acetonitrile to give the corresponding sensitively fluorescent derivatives. The application of this method to the analysis of long chain fatty acids in plasma is also investigated. The LC separation shows good selectivity and reproducibility for fatty acids derivatives. The R.S.D. (n = 6) for each fatty acid derivative are <4%. The detection limits are at 45-68 fmol levels for C-14-C-20 fatty acids and even lower levels for

Determination of alcohols by high-performance liquid chromatography with fluorimetric detection after pre-column derivatisation with carbazole-9-N-acetic acid and chromatographic behaviour of alcoholic derivatives

Alcohols were derivatised to their carbazole-9-N-acetic acid (CRA) esters with 1-ethyl-3-(3-dimethylaminopropyl)carbodiimide hydrochloride (EDC . HCl) as the dehydrating agent. Studies on derivatisation conditions indicated that the coupling reaction proceeded rapidly and smoothly in the presence of a base catalyst in acetonitrile to give the corresponding sensitively fluorescent derivatives. The retention behaviour of alcohol derivatives was investigated by varying mobile phase compositions (ACN-water and MeOH-water). The parameters from the equation log k'=A-BX were evaluated by retention data of derivatives using an isocratic elution with different mobile phases. The results indicated that the parameters derived allowed computation of retention factors in good agreement with experiments. At the same time, a general equation was derived that makes possible predictions of partition coefficient in binary mobile phases with different proportions of organic solvent to water based on some simple regression analysis. The LC separation for the derivatised alcohols containing higher carbon alcohols showed good reproducibility on a reversed-phase C-18 column with gradient elution. The detection limits (excitation at 335 nm, emission at 360 nm) for derivatised alcohols (signal-to-noise ratio=3:1) were in the range of 0.1-0.4 pg per injection. (C) 2001 Elsevier Science B.V. All rights reserved.