西藏林周县江多乡发现吐蕃王朝墓葬群

2001年,中国地质科学院地质力学研究所西藏项目组在开展青藏高原空白区1:25万当雄幅区域地质调查过程中,在拉萨市属林周县旁多区江多乡发现唐代吐蕃王朝墓葬1处.吐蕃王朝存在于公元前2世纪～公元9世纪,当时时兴墓葬.……     

丝绸之路青海道吐蕃时期墓葬出土木材记载的森林干扰史

森林动态与气候变化及人类活动有着紧密的联系,了解森林干扰的发生历史对准确预测全球变暖背景下的森林动态具有重要意义,也可为理解历史时期的气候变化和人地关系演变提供线索.文章利用丝绸之路青海道沿线吐蕃时期3个墓葬中出土的78棵祁连圆柏(Juniperus przewalskii Komarov)原木作为研究对象,利用树木年...     

雅鲁藏布江中游及昌果沟遗址古环境分析

西藏拉萨昌果沟遗址位于雅鲁藏布江中游支流的阶地上,是重要的新石器时代遗址.为探讨昌果沟遗址附近的古环境,对遗址附近开展地貌调查,在遗址北面约1 km处选取1个全新世风成沉积剖面进行光释光测年和环境指标分析,在雅鲁藏布江中游选2个阶地剖面进行光释光测年分析;此外,还总结了雅鲁藏布江中游23个全新世古土壤/泥炭的测年数据,进行概率密度分析,试图揭示区域的环境演化特征.研究表明:全新世古土壤/泥炭年代的概率密度可以较好地反映区域气候变化,9.0~6.0 ka古土壤/泥炭发育在波动中增强,气候由冷干向暖湿转换;6.0~2.9 ka古土壤/泥炭发育最强,气候相对温干;2.9 ka后鲜有古土壤/泥炭发育,气候变得冷干,史前人类活动受限.4.5 ka之后雅鲁藏布江中游及其支流一级阶地的形成为新石器时期先民提供农业耕作的场所,古土壤的发育为农作物提供了丰富的营养.1.4~1.1 ka期间(吐蕃王朝时期)局部地区有古土壤发育,气候好转.     

高密度电法应用于考古工作的实验初探

试验主要研究高密度电阻率法应用于考古工作中的可行性与可靠性.试验采用了水槽和田野模型实验的形式,根据物理"相似性"原则,通过模型模拟古代墓葬中的各种建筑材料在视电阻率反演等值线图上的反映,讨论了电极距、电极总数、装置类型、古墓葬埋藏环境、墓葬建筑结构等因素对反演等值线图的影响,得出一些结论.     

新疆吐鲁番胜金店墓地小麦遗存加工处理方式初探

脱粒是谷物加工处理的重要环节之一.本文选择新疆吐鲁番胜金店墓地M9墓葬出土大量保存完好的小麦遗存进行原始脱粒方式分析,并尝试结合现代小麦原始脱粒方式模拟实验,将现代模拟实验结果与古代材料进行对比分析,从而初步探讨新疆吐鲁番地区先民的小麦脱粒方式.本文首先对胜金店墓地M9墓葬出土的小麦遗存进行初步分类,将不同的小麦脱粒产品与副产品(麦秆、花序轴、小穗轴等)进行分析和统计;其次设计并完成现代小麦脱粒模拟实验,包括手搓、徒手摔打、木棍击打等3种相对原始的小麦脱粒方式,统计不同脱粒方式所产生的小麦加工产品与副产品的组合比例;将现代模拟实验所得结果与M9墓葬出土小麦遗存进行进一步对比分析.研究结果表明,在距今约2000多年前,新疆吐鲁番胜金店先民可能使用木棍击打方式对小麦进行脱粒.     

乌鲁木齐河源1号冰川不同时期雪层剖面及成冰带对比研究

对20世纪60年代、80年代和21世纪初天山乌鲁木齐河源1号冰川(以下简称1号冰川)雪层剖面特征、成冰带的对比分析研究,发现自20世纪60年代以来,1号冰川雪层剖面厚度明显减薄,结构变得简单,各层界限变得模糊.成冰带类型及其分布发生了明显变化,60年代存在于冷气候条件下的冷渗浸带,80年代被渗浸带所替代.21世纪初,1号冰川成冰带变化更为显著,尤其是东支,顶部已具有消融带特征.研究表明,20世纪80年代以来河源区气候变暖是导致上述变化的主要原因.     

桂林甑皮岩遗址岩溶地下水水害成因及防治对策

桂林甑皮岩遗址自1973年试掘以来,出土了古人类骨架、火塘、墓葬、石器、蚌器、陶器、动植物化石等大量的较为珍贵的实物资料,成为我国南方的一个重要的新石器人类遗址.2001年被列入国家级重点文物保护单位.然遗址在1994年汛期遭受洪水浸泡,致使多个探方隔梁崩塌,探方文化土层先后出现不同程度的崩塌或下沉现象.为了暂时性抢救...     

全球气候变化研究的新认识——IPCC第三次气候评价报告第一工作组报告概要

政府间气候变化专门委员会 (IPCC)在前两次气候变化评价报告的基础上 ,结合最近 5年气候变化研究新成果 ,进行了 IPCC第三次全球气候的评价工作。IPCC第一工作组于 2 0 0 1年 1月 1 7- 2 0日在上海召开了第八次工作组会议 ,通过了供决策者参考的报告概要。下面是该报告的摘要性结论。1日益增多的大量观测结果表明 :地球正在变暖并伴随气候系统的其它变化1 .1　 2 0世纪全球平均地表温度增加了 0 .6℃左右(1 )全球平均地表温度自 1 861年以来一直在增高 ,2 0世纪增加了 0 .6± 0 .2℃。这个数据比 1 994年的 IPCC第二次气候评价报告高…     

地球物理方法勘探古墓实例

一九七八年三月,河南省固始县城东南两公里处的侯古堆北侧在取土时发现一个古墓的陪葬坑。然而,主墓葬的具体位置究竟在什么地方？是考古发掘中急待解决的难题。     

丝绸之路东端大都会粮仓中的谷物:大同操场城北魏太官粮储遗址炭化粟的C、N稳定同位素分析

施肥等农田管理手段是提高粮食产量的重要途径,直接关乎先民的温饱乃至社会的安定.目前,施肥等农田管理手段的应用及对特定时空范围的影响程度等,依然缺乏深入的研究.作为丝绸之路东端的大都会,北魏王朝的都城平城在其建立之初及其后的近百年,人口数量剧增且稳定在百万左右,稳定、优质的粮食供给日益成为帝国稳定和发展的根基.本文对大同...     

Isotopic systematics of He,Ar, S,Cu, Ni,Re, Os,Pb, U,Sm, Nd,Rb, Sr,Lu, and Hf in the rocks and ores of the Norilsk deposits

This paper reports the first results of a study of 11 isotope systems (³He/⁴He, ⁴⁰Ar/³⁶Ar, ³⁴S/³²S, ⁶⁵Cu/⁶³Cu, ⁶²Ni/⁶⁰Ni, ⁸⁷Sr/⁸⁶Sr, ¹⁴³Nd/¹⁴⁴Nd, ^206–208Pb/²⁰⁴Pb, Hf–Nd, U–Pb, and Re–Os) in the rocks and ores of the Cu–Ni–PGE deposits of the Norilsk ore district. Almost all the results were obtained at the Center of Isotopic Research of the Karpinskii All-Russia Research Institute of Geology. The use of a number of independent genetic isotopic signatures and comprehensive isotopic knowledge provided a methodic basis for the interpretation of approximately 5000 isotopic analyses of various elements. The presence of materials from two sources, crust and mantle, was detected in the composition of the rocks and ores. The contribution of the crustal source is especially significant in the paleofluids (gas–liquid microinclusions) of the ore-forming medium. Crustal solutions were probably a transport medium during ore formation. Air argon is dominant in the ores, which indicates a connection between the paleofluids and the atmosphere. This suggests intense groundwater circulation during the crystallization of ore minerals. The age of the rocks and ores of the Norilsk deposits was determined. The stage of orebody formation is restricted to a narrow age interval of 250 ± 10 Ma. An isotopic criterion was proposed for the ore-bearing potential of mafic intrusions in the Norilsk–Taimyr region. It includes several interrelated isotopic ratios of various elements: He, Ar, S, and others.     

高压微波消解法测定醋酸纤维过滤器采集的微尘粒子中的砷镉钴铬铜铁锰镍铅钒锌

最新的流行病学研究表明,空气中较高浓度的悬浮细颗粒可能对人类的健康有不利的影响。根据该项研究显示,由于心脏病、慢性呼吸问题和肺功能指标恶化而导致死亡率的升高与细尘粒子有关。这些研究结果已经促使欧盟于1999年4月出台了限制空气中二氧化硫、二氧化氮、氧化氮、铅和颗粒物含量的法案(1999/30/EC),对各项指标包括对可吸入PM10颗粒的浓度提出了新的限制性指标。PM10颗粒是指可以通过预分级器分离采集的气体动力学直径小于10μm的细颗粒。目前研究的兴趣重点逐步偏向PM2.5这些更细微颗粒物,PM2.5这种颗粒物对健康有明显的不利影响。在欧盟指令2008/50/EC中,对PM10和PM2.5都提     

Wavelength-dispersive X-ray fluorescence spectrometric determination of Sc, V, Cr, Co, Ni, Cu, Zn, Rb, Sr, Y, Zr, Nb, Ba, Pb, and Th in komatiites

Komatiites are mantle-derived ultramafic volcanic rocks. Komatiites have been discovered in several States of India, notably in Karnataka. Studies on the distribution of trace-elements in the komatiites of India are very few. This paper proposes a simple, accurate, precise, rapid, and non-destructive wavelength-dispersive x-ray fluorescence (WDXRF) spectrometric technique for determining Sc, V, Cr, Co, Ni, Cu, Zn, Rb, Sr, Y, Zr, Nb, Ba, Pb, and Th in komatiites, and discusses the accuracy, precision, limits of detection, x-ray spectral-line interferences, inter-element effects, speed, advantages, and limitations of the technique. The accuracy of the technique is excellent (within 3%) for Sc, V, Cr, Co, Ni, Cu, Zn, Rb, Sr, Zr, Nb, Ba, Pb, and Th and very good (within 4%) for Y. The precision is also excellent (within 3%) for Sc, V, Cr, Co, Ni, Cu, Zn, Rb, Sr, Y, Zr, Nb, Ba, Pb, and Th. The limits of detection are: 1 ppm for Sc and V; 2 ppm for Cr, Co, and Ni; 3 ppm for Cu, Zn, Rb, and Sr; 4 ppm for Y and Zr; 6 ppm for Nb; 10 ppm for Ba; 13 ppm for Pb; and 14 ppm for Th. The time taken for determining Sc, V, Cr, Co, Ni, Cu, Zn, Rb, Sr, Y, Zr, Nb, Ba, Pb, and Th in a batch of 24 samples of komatiites, for a replication of four analyses per sample, by one operator, using a manual WDXRF spectrometer, is only 60 hours.     

Regional distribution of Al,B, Ba,Ca, K,La, Mg,Mn, Na,P, Rb,Si, Sr,Th, U and Y in terrestrial moss within a 188,000 km2 area of the central Barents region: influence of geology,seaspray and human activity

Five hundred and ninety-eight samples of terrestrial moss (Hylocomium splendens and Pleurozium schreberi) collected from a 188,000 km² area of the central Barents region (NE Norway, N Finland, NW Russia) were analysed by ICP-AES and ICP-MS. Analytical results for Al, B, Ba, Ca, K, La, Mg, Mn, Na, P, Rb, Si, Sr, Th, U and Y concentrations are reported here. Graphical methods of data analysis, such as geochemical maps, cumulative frequency diagrams, boxplots and scatterplots, are used to interpret the origin of the patterns for these elements. None of the elements reported here are emitted in significant amounts from the smelting industry on the Kola Peninsula. Despite the conventional view that moss chemistry reflects atmospheric element input, the nature of the underlying mineral substrate (regolith or bedrock) is found to have a considerable influence on moss composition for several elements. This influence of the chemistry of the mineral substrate can take place in a variety of ways. (1) It can be completely natural, reflecting the ability of higher plants to take up elements from deep soil horizons and shed them with litterfall onto the surface. (2) It can result from naturally increased soil dust input where vegetation is scarce due to harsh climatic conditions for instance. Alternatively, substrate influence can be enhanced by human activity, such as open-cast mining, creation of ‘technogenic deserts’, or handling, transport and storage of ore and ore products, all of which magnify the natural elemental flux from bedrock to ground vegetation. Seaspray is another natural process affecting moss composition in the area (Mg, Na), and this is most visible in the Norwegian part of the study area. Presence or absence of some plant species, e.g., lichens, seems to influence moss chemistry. This is shown by the low concentrations of B or K in moss on the Finnish and Norwegian side of the (fenced) border with Russia, contrasting with high concentrations on the other side (intensive reindeer husbandry west of the border has selectively depleted the lichen population).     

Petrographic, mineralogy, and geochemistry of coals of Pabedana, Kerman Province, Central Iran

This paper discusses the result of the detailed investigations carried out on the coal characteristics, including coal petrography and its geochemistry of the Pabedana region. A total of 16 samples were collected from four coal seams d2, d4, d5, and d6 of the Pabedana underground mine which is located in the central part of the Central-East Iranian Microcontinent. These samples were reduced to four samples through composite sampling of each seam and were analyzed for their petrographic, mineralogical, and geochemical compositions. Proximate analysis data of the Pabedana coals indicate no major variations in the moisture, ash, volatile matter, and fixed carbon contents in the coals of different seams. Based on sulfur content, the Pabedana coals may be classified as low-sulfur coals. The low-sulfur contents in the Pabedana coal and relatively low proportion of pyritic sulfur suggest a possible fresh water environment during the deposition of the peat of the Pabedana coal. X-ray diffraction and petrographic analyses indicate the presence of pyrite in coal samples. The Pabedana coals have been classified as a high volatile, bituminous coal in accordance with the vitrinite reflectance values (58.75–74.32 %) and other rank parameters (carbon, calorific value, and volatile matter content). The maceral analysis and reflectance study suggest that the coals in all the four seams are of good quality with low maceral matter association. Mineralogical investigations indicate that the inorganic fraction in the Pabedana coal samples is dominated by carbonates; thus, constituting the major inorganic fraction of the coal samples. Illite, kaolinite, muscovite, quartz, feldspar, apatite, and hematite occur as minor or trace phases. The variation in major elements content is relatively narrow between different coal seams. Elements Sc,, Zr, Ga, Ge, La, As, W, Ce, Sb, Nb, Th, Pb, Se, Tl, Bi, Hg, Re, Li, Zn, Mo, and Ba show varying negative correlation with ash yield. These elements possibly have an organic affinity and may be present as primary biological concentrations either with tissues in living condition and/or through sorption and formation of organometallic compounds.     

Mercury,arsenic, antimony,and selenium contents of sediment from the Kuskokwim River,Bethel, Alaska,USA

The Kuskokwim River at Bethel, Alaska, drains a major mercury-antimony metallogenic province in its upper reaches and tributaries. Bethel (population 4000) is situated on the Kuskokwim floodplain and also draws its water supply from wells located in river-deposited sediment. A boring through overbank and floodplain sediment has provided material to establish a baseline datum for sediment-hosted heavy metals. Mercury (total), arsenic, antimony, and selenium contents were determined; aluminum was also determined and used as normalizing factor. The contents of the heavy metals were relatively constant with depth and do not reflect any potential enrichment from upstream contaminant sources.     

Coprecipitation of Ti,Mo, Sn and Sb with fluorides and application to determination of B,Ti, Zr,Nb, Mo,Sn, Sb,Hf and Ta by ICP-MS

We examined the coprecipitation behavior of Ti, Mo, Sn and Sb in Ca–Al–Mg fluorides under two different fluoride forming conditions: at < 70 °C in an ultrasonic bath (denoted as the ultrasonic method) and at 245 °C using a Teflon bomb (denoted as the bomb method). In the ultrasonic method, small amounts of Ti, Mo and Sn coprecipitation were observed with 100% Ca and 100% Mg fluorides. No coprecipitation of Ti, Mo, Sn and Sb in Ca–Al–Mg fluorides occurred when the sample was decomposed by the bomb method except for 100% Ca fluoride. Based on our coprecipitation observations, we have developed a simultaneous determination method for B, Ti, Zr, Nb, Mo, Sn, Sb, Hf and Ta by Q-pole type ICP-MS (ICP-QMS) and sector field type ICP-MS (ICP-SFMS). 9–50 mg of samples with Zr–Mo–Sn–Sb–Hf spikes were decomposed by HF using the bomb method and the ultrasonic method with B spike. The sample was then evaporated and re-dissolved into 0.5 mol l^− 1 HF, followed by the removal of fluorides by centrifuging. B, Zr, Mo, Sn, Sb and Hf were measured by ID method. Nb and Ta were measured by the ID-internal standardization method, based on Nb/Mo and Ta/Mo ratios using ICP-QMS, for which pseudo-FI was developed and applied. When 100% recovery yields of Zr and Hf are expected, Nb/Zr and Ta/Hf ratios may also be used. Ti was determined by the ID-internal standardization method, based on the Ti/Nb ratio from ICP-SFMS. Only 0.053 ml sample solution was required for measurement of all 9 elements. Dilution factors of ≤ 340 were aspirated without matrix effects. To demonstrate the applicability of our method, 4 carbonaceous chondrites (Ivuna, Orgueil, Cold Bokkeveld and Allende) as well as GSJ and USGS silicate reference materials of basalts, andesites and peridotites were analyzed. Our analytical results are consistent with previous studies, and the mean reproducibility of each element is 1.0–4.6% for basalts and andesites, and 6.7–11% for peridotites except for TiO₂.