广西融水杆洞铜矿床地质特征初探

杆洞铜矿床赋存于广西桂北最老地层─—中元古界四堡群中，矿体呈脉状产于杆洞花岗斑岩体及其外接触带围岩中，受ＮＮＥ向断裂裂隙构造控制明显，矿石具细脉浸染状、块状构造，矿石平均品位Ｃｕ０．７８５—１．７４８％，矿石矿物主要为黄铜矿、斑铜矿、辉铜矿、黄铁矿，局部伴生方铅矿、闪锌矿，脉石矿物有石英、绢云母、绿泥石、黑云母，围岩蚀变主要为石英绢云母化与绿泥石化、黄铁矿化、硅化，据此认为属岩浆热液交代充填脉型矿床。     

A 3600 years paleoclimatic change inferred from organic δ13C and TOC/TN of the Gucheng Lake sediments, southeast China

A 6.2 m thick core of Gucheng Lake sediment provided a 3600 years record of climate change. The contents of the TOC in the core changed from 2.63% to 8.48%, and the δ¹³C values of organic matter were from −21.54% to −27.3%. The TOC/TN ratios indicated that the organic materials in sediments were from lake plankton and land-derived plants. The 2.9–22 m core interval with high TOC/TN ratios, low δ¹³C values and low contents of TOC indicated a cold climate stage. The 6.2–5.5 m and 0.4–0.1 m intervals were characterized by low TOC/TN ratios, high δ¹³C values and high contents of TOC, and reflected temperate climate stages. Project 49372129 supported by NSFC.     

Norwegian sea‐surface palaeoenvironments of marine oxygen‐isotope stage 3: the paradoxical response of dinoflagellate cysts

High‐resolution marine palynological data have been obtained from two very long sediment cores (MD952009 and MD952010) retrieved from the southern Norwegian Sea. The dinoflagellate cyst assemblages show pronounced fluctuations in composition, which correlate strongly with magnetic susceptibility records and also mimic the δ¹⁸O signal of the GISP2 Greenland ice‐core. If focusing on the period from 48 to 30 cal. kyr BP, this correlation suggests a paradoxical response of the sea‐surface environments to the atmospheric conditions over Greenland: when the Greenland δ¹⁸O signal reflects warm interstadial conditions, the Norwegian Sea depicts cold sea‐surface temperatures with quasi‐perennial sea‐ice cover (based on dinoflagellate cysts). In contrast, when the Greenland δ¹⁸O records cold stadial periods, the Norwegian Sea‐surface temperatures are warm (based on dinoflagellate cysts), probably linked to inflow of the North Atlantic Drift. These results, similar in both cores, are contrary to those of previous studies and shed light on a possible decoupling of Norwegian sea surface‐water conditions and atmospheric conditions over Greenland. This decoupling could be linked to an atmosphere–ocean system behaving similar to that which the Northern Hemisphere is experiencing at present, i.e. strongly variable owing to the North Atlantic Oscillation. Copyright © 2002 John Wiley & Sons, Ltd.     

A multivariate statistical study of copper mineralization in the central section of Mosaboni Mine, Eastern Singhbhum, India

A multivariate statistical analysis was carried out with log-transformed values of Cu, Ni, Co, Pb, Zn, Ag, Cr, Mn, Ca, and Sr in several sets of samples collected across the mineralized base metal zone in sheared soda granite, feldspathic schist, and chlorite schist from the central section of Mosaboni Mine of the famous Singhbhum Copper Belt of eastern India. Linear correlation coefficient matrices of two sets of ore samples (>0.5% Cu)—one from levels 18 and 21 and the other from levels 25 and 28—indicate two well-defined and distinct clusters comprising Cu, Ni, Co, Pb, and Zn on one hand and Ca, Sr, and Mn on the other. Varimax-rotatedR-mode factor analysis of two above-noted sample sets, taken along with available geologic information, indicates that over 80% of the variability in data matrices for 9–10 elements can be accounted for by four distinct processes: (a) an early phase of copper mineralization which apparently replaced Mn, Ca, and Sr in the host rock; (b) a silicate-cum-oxide phase of crystallization/recrystallization of host rock; (c) remobilization of sulfide-forming ore elements (Cu, Ni, Co, Pb, and Zn); and (d) a phase of mineralization of Ag which appears to have replaced Cr, Ca and Cu. Process (c) was quantitatively most important. Factor score studies are suggestive of preferred introduction of Ni, Co, Pb, and Zn along central parts of preexisting copper-mineralized zones.     

Continuous fluorescence assessment of organic matter variability on the Bournbrook River,Birmingham, UK

Continuous monitoring of dissolved organic matter (DOM) character and concentration at hourly resolution is rare, despite the importance of analysing organic matter variability at high‐temporal resolution to evaluate river carbon budgeting, river water health by detecting episodic pollution and to determine short‐term variations in chemical and ecological function. The authors report a 2‐week experiment performed on DOM sampled from Bournbrook, Birmingham, UK, an urban river for which spectrophotometric (fluorescence, absorbance), physiochemical (dissolved organic carbon [DOC], electrical conductivity, pH) and isotopic (D/H) parameters have been measured at hourly frequency. Our results show that the river had sub‐daily variations in both organic matter concentration and characteristics. In particular, after relatively high‐magnitude precipitation events, organic carbon concentration increased, with an associated increase in intensity of both humic‐like and tryptophan‐like fluorescence. D/H isotopic ratio demonstrates different hydrological responses to different rainfall events, and organic matter character reflects this difference. Events with precipitation < 2 mm typically yielded isotopically heavy water with relatively hydrophilic DOM and relatively low specific absorbance. Events with precipitation > 2 mm had isotopically lighter water with higher specific absorbance and a decrease in the proportion of microbially derived to humic‐like fluorescence. In our heavily urbanized catchment, we interpret these signals as one where riverine DOM is dominated by storm sewer‐derived ‘old’ organic matter at low‐rainfall amounts and a mixed signal at high‐precipitation amounts where ‘event’ surface runoff‐derived organic matter dominate during storm sewer and combined sewer overflow routed DOM. Copyright © 2009 John Wiley & Sons, Ltd.     

Microscale Simultaneous Measurement of Carbon and Nitrogen Isotopes on Natural Diamond

Simultaneous analysis of carbon and nitrogen isotope ratios by SIMS was applied for the first-time to a natural diamond from the Kelsey Lake kimberlite, State Line Distinct, Colorado (UWD-1). This in situ procedure is faster, reduces sample size for analysis, and measures both isotope ratios from a single ~ 10 μm diameter pit, a critical advantage for zoned diamonds. The carbon isotope ratio (expressed as δ¹³C_VPDB) of the bulk UWD-1 crystal, determined by the conventional combustion method in the present study, is -5.9‰ ± 0.2‰ (VPDB, 2s). Nitrogen mass fraction ([N]) and isotope ratio (expressed as δ¹⁵N_Air) were determined by stepwise combustion and gas-source mass-spectrometry, resulting in 553 ± 64 μg g^-1 and -6.7‰ ± 1.1‰ (Air, 2s), respectively. Secondary ions of ¹²C₂^-, ¹²C¹³C^-, ¹²C¹⁴N^-, and ¹²C¹⁵N^- were simultaneously measured by SIMS using three Faraday cups and one electron multiplier. The spot-to-spot reproducibility of δ¹³C and δ¹⁵N values for the UWD-1 (178 spots on sixteen chips, 10 μm spots), were 0.3‰ and 1.6‰, respectively (2s). While ¹²C¹⁴N^-/¹²C₂^- ratios, which are an indicator for [N], varied up to 12% among these sixteen chips, such variation did not correlate with either δ¹³C or δ¹⁵N values. We propose that UWD-1 is a suitable reference sample for microscale in situ analysis of δ¹³C and δ¹⁵N values in diamond samples.     

High-precision analysis of carbon isotopic composition for individual CO2 inclusions via Raman spectroscopy to reveal the multiple-stages evolution of CO2- bearing fluids and melts

The carbon isotopic composition of CO₂ inclusions trapped in minerals reflects the origin and evolution of CO₂-bearing fluids and melts, and records the multiple-stages carbon geodynamic cycle, as CO₂ took part in various geological processes widely. However, the practical method for determination isotope composition of individual CO₂ inclusion is still lacking. Developing a microanalytical technique with spatial resolution in micrometers to precisely determinate the δ¹³C value of individual CO₂ inclusion, will make it possible to analyze a tiny portion of a zoning mineral crystal, distinguish the differences in micro-scale, and possible to find many useful information that could not be obtained with the bulk extraction and analysis techniques. In this study, we systematically collected Raman spectra of CO₂ standards with different δ¹³C values (?34.9 ‰ to 3.58 ‰) at 32.0 °C and from ～7.0 MPa to 120.0 MPa, and developed a new procedure to precisely determinate the δ¹³C value of individual CO₂ inclusion. We investigated the relationship among the Raman peak intensity ratio, δ¹³C value, and CO₂ density, and established a calibration model with high accuracy (0.5 ‰?1.5 ‰), sufficient for geological application to distinguish different source of CO₂ with varying δ¹³CO₂. As a demonstration, we measured the δ¹³C values and the density of CO₂ inclusions in the growth zones of alkali basalt-hosted corundum megacrysts from Changle, Shandong Province. We found the significant differences of density and δ¹³C between the CO₂ inclusions in the core of corundum and those inclusions in the outer growth zones, the δ¹³C value decreases from core to rim with decreasing density: δ¹³C values are from ?7.5 ‰ to ?9.2 ‰ for the inclusions in the core, indicating the corundum core was crystallized from mantle-derived magmas; from ?13.5 ‰ to ?18.5 ‰ for CO₂ inclusions in zone 1 and from ?16.5 ‰ to –22.0 ‰ for inclusions in zone 2, indicating the outer zones of corundum grew in a low δ¹³C value environment, resulted from an infilling of low δ¹³C value fluid and/or degassing of the ascending basaltic magma.     

Mineralization of the Liwu large-scale stratiform copper deposits in Sichuan Province,China: Constraints from fluid inclusions

The Liwu stratiform copper deposit is located in the northwestern Jianglang dome, western China. Current studies mainly focus on the genetic type and mineralization of this deposit. Detailed fluid inclusion characteristics of metallogenic period quartz veins were studied to reveal the ore-forming fluid features. Laser Raman analysis indicates that the ore-forming fluids is a H₂O-NaCl-CH₄ (-CO₂) system. Fluid inclusions microthermometry shows a homogenization temperature of 181–375°C and a salinity of 5.26%–16.99% for the disseminated-banded Cu-Zn mineralization; but a homogenization temperature of 142–343°C and a salinity of 5.41%–21.19% for the massive-veined Cu-Zn mineralization. These features suggest a medium-high temperature and a medium salinity for the ore-forming fluids. H-O isotopic data indicates that the ore-forming fluids were mainly from the metamorphic and magmatic water, plus minor formation water. And sulfur isotopic data indicates that sulfur was mainly derived from the formation and magmatic rocks. Metallogenesis of the disseminated-banded mineralization was mainly correlated with fluid mixing and water-rock reaction; whereas that of the massive-veined mineralization was mainly correlated with fluid boiling. The genetic type of the deposit is a medium-high temperature hydrothermal deposit related to magmatism and controlled by shear zones. This study is beneficial to understand the stratiform copper deposit.©2023 China Geology Editorial Office.     

四川盆地东部地区早中三叠世蒸发岩的锶同位素特征及其地质意义

锶同位素已经成为全球海平面变化、造山运动、古气候和古环境等全球地质事件研究与对比的有效工具之一。本文以四川盆地东部地区早中三叠世蒸发岩的野外剖面和钻孔岩心为主要研究对象,测试了碳酸盐岩、硫酸盐岩和石盐岩的锶同位素组成,并建立了相应的锶同位素演化曲线。研究结果显示,碳酸盐岩的⁸⁷Sr/⁸⁶Sr值平均为0.707 895,硬石膏岩的⁸⁷Sr/⁸⁶Sr值平均为0.708 174,石盐岩的⁸⁷Sr/⁸⁶Sr值平均为0.708 177,同时碳酸盐岩的⁸⁷Sr/⁸⁶Sr值从早三叠世的0.707 413快速增加到中三叠世早期的0.708 515,而后呈现下降趋势。从总体上看,这些⁸⁷Sr/⁸⁶Sr值与全球早中三叠世同期的⁸⁷Sr/⁸⁶Sr值数据接近,说明四川盆地东部地区早中三叠世钾盐的物质来源大部分为海水,并沉积于海相沉积环境,同时由于火山...     

A Comparison Study on the δD Value of Polycyclic Aromatic Hydrocarbons in Hydrous Pyrolysate of Herbaceous Peat with Different Water Medium

To investigate the influence of diagenetic water media on the hydrogen isotopes of individual sedimentary aromatic compounds, a series of hydrous pyrolyses were conducted on herbaceous peat. Polycyclic aromatic hydrocarbons (PAHs) in hydrous pyrolysed samples and their hydrogen isotopic composition characteristics were studied. The aqueous medium demonstrated a significant influence on the hydrogen isotopic composition of the individual PAHs generated during pyrolysis. The results showed that the PAHs formed after pyrolysis in the presence of a saltwater medium with high δD value from a salt lake had a heavy hydrogen isotopic composition. The PAHs formed after pyrolysis in the presence of a fresh water medium with low δD value from a swamp had a light hydrogen isotopic composition. The difference in the average PAH δD value between the two hydrous experiments varied from –174‰ to –109‰, suggesting that the hydrogen isotopic composition of individual sedimentary PAHs can reflect the source of the diagenetic water medium. In addition, a comparative study found that the hydrogen isotopes of PAHs were superior to those of n-alkanes in the same sample for diagenetic water indications. The results indicated that the exchange of water-derived inorganic hydrogen and organic hydrogen was more intensive in freshwater experiments than in saltwater experiments. With an increase in the simulation temperature, the average δD value of PAHs generated in the hydrous simulation experiments showed an increasing trend, reflecting that the δD value of sedimentary PAHs formed with the participation of diagenetic water media was still closely related to the thermal maturity of organic matter. Comparative studies showed that the δD values of different types of organic compounds produced by hydrous pyrolysis of peat were in the order, PAHs > n-alkanes > methane.