普朗斑岩铜矿包裹体、同位素研究及成矿时代

普朗斑岩铜矿产于印支-燕山早期普朗复式斑岩体中。成矿流体来源广、盐度高,成矿温度从高温440℃到低温120℃,集中在160℃-240℃、280℃-320℃、340℃-380℃三阶段,多期次、多阶段性,与斑岩成矿作用特征一致。硫同位素3δ4SCDT‰T为（-2.23-3.75）‰,显示单一深源岩浆硫。岩体黑云母等40Ar-39Ar和矿石石英-辉钼矿Re-Os同位素年龄为206.4M a-213±3.8M a,属岛孤斑岩型铜矿床。     

Origin of high H2S concentrations in the Upper Permian Changxing reservoirs of the Northeast Sichuan Basin,China

Intense thermochemical sulfate reduction (TSR) and up to 18% H₂S are found in the Upper Permian Changxing Formation (P₃ch) in the northeast (NE) Sichuan Basin, China, despite that rare gypsum or anhydrite was found in this formation. Here, we present new concentration data of carbonate-associated sulfate (CAS) from carbonate host rocks, C, O, and Sr isotope data for TSR-related calcites, and S isotope data for sulfur compounds obtained during this study. These data along with spatial-temporal changes in palaeogeopressure conditions, hydraulic conductivity and the physical capacity indicate that the H₂S was generated locally from TSR within the P₃ch reservoirs. We propose that the reactive sulfates were derived from CAS released during dolomitization and recrystallization of earlier dolomite within the P₃ch Fm. and from the cross-formational migration of evaporative brines from the Lower Triassic Feixianguan Formation (T₁f) to P₃ch Fm. Our calculation shows that the two sources could provide enough SO₄²⁻ for the generation of H₂S within the P₃ch reservoirs. Early downward migration of sulfate-rich evaporative brines from the T₁f formation occurred in near-surface and shallow burial diagenetic settings (mainly <1000 m). The evaporative brines seeped into porous grainstones and displaced preexisting seawater, causing pervasive dolomitization within the P₃ch Fm. Subsequently, TSR calcites precipitated from the pore water have high Sr concentrations (up to 7767 ppm), close to the T₁f TSR calcites, and ⁸⁷Sr/⁸⁶Sr ratios mainly from 0.7074 to 0.7078, which are significantly higher than those of Late Permian seawater but within the range of early Triassic seawater.     

An analysis and comparison of observed Pleistocene South Carolina (USA) shoreline elevations with predicted elevations derived from Marine Oxygen Isotope Stages

Geological maps of South Carolina, covering > 6800 km², confirm the existence of eight preserved Pleistocene shorelines above current sea level: Marietta (+ 42.6 m), Wicomico (+ 27.4 m), Penholoway (+ 21.3 m), Ladson (+ 17.4 m), Ten Mile Hill (+ 10.7 m), Pamlico (+ 6.7 m), Princess Anne (+ 5.2 m), and Silver Bluff (+ 3 m). Current geochronologic data suggest that these eight shorelines correlate with Marine Oxygen Isotope Stages (MIS) as follows: Marietta—older than MIS 77; Wicomico—MIS 55–45; Penholoway—MIS 19 or 17; Ladson—MIS 11; Ten Mile Hill—MIS 7; Pamlico—MIS 5; Princess Anne—MIS 5; and Silver Bluff—MIS 5 or 3. Except for the MIS 5e Pamlico, and possibly the MIS 11 Ladson, the South Carolina elevations are higher than predicted by isotope proxy-based reconstructions. The < 4 m of total relief from the Pamlico to the Silver Bluff shoreline in South Carolina, for which other reconstructions suggest an expected relief of ~ 80 m, illustrates the lack of match. Our results suggest that processes affecting either post-depositional changes in shoreline elevations or the creation of proxy sea-level estimates must be considered before using paleo sea-level position on continental margins.     

应用单体碳同位素分析技术探析农田土壤中多环芳烃的植物降解过程

长期以来,研究者在探讨土壤中多环芳烃(PAHs)的降解及修复过程中,缺乏简便有效的手段对化合物的降解动态进行定量研究。前人尝试用投加实验、对比采用降解措施前后污染物的浓度变化、模型计算等方法研究PAHs的降解过程,其结果常互相矛盾,或不能真实反映复杂的实际环境。本文应用单体碳同位素技术对农田土壤中多环芳烃的植物降解过程进行定量表征,采集了某地农田表土作为供试土壤,选择玉米作为供试作物,开展了作物对土壤中PAHs降解及消除过程的研究。气相色谱-质谱分析结果表明,培养所用的玉米原始土及分4批收集的空白土、根际土、非根际土样品中16种PAHs的浓度总和(∑PAHs)平均分别为380.8 ng/g、(281.5±34.7) ng/g、(272.2±11.6) ng/g和(299.8±37.9) ng/g;玉米生长期间,各土壤样品 的∑PAHs均比原始土壤有所下降,但除3环化合物(苊烯、苊、芴、菲、蒽)外,其他化合物并未随玉米的生长表现出显著趋势。与玉米根、叶倾向于富集低环PAHs化合物相对应,可以判断植物对土壤中的低环化合物去除作用最为显著。各采样时期玉米根际土、非根际土和空白土壤样品中多环芳烃单体化合物的碳同位素分馏值(δ¹³C)在-34.31‰~-23.95‰之间,且除芘外的其他化合物的δ¹³C值随时间呈现逐步变轻的趋势,波动值位于-0.6‰~-9.0‰之间;本文对于PAHs单体化合物,尤其是4、5环化合物,在玉米降解过程中的碳同位素分馏与浓度变化之间未发现明显关系。考虑3环以下的PAHs化合物更倾向于被降解和清除,且其碳、氢同位素分馏情况更容易被观察到,因此稳定同位素分析更有助于探明该类单体多环芳烃污染物在环境中的迁移、转化规律。     

11颗行星际尘粒中的锂,硼同位素丰度分析

我们首次测量了4颗行星际尘粒(IDPs)中的~6Li/~7Li,~(10)B/~(11)B。它们的平均值分别是(8.40±0.37)×10~(-2)和(2.40±0.18)×10~(-2),随后又精确测量了7颗IDPs~6Li/Li的同位素丰度。     

Lu–Hf constraints on pre-, syn,and post-collision associations of the Gurupi Belt,Brazil: Insights on the Rhyacian crustal evolution

The Gurupi Belt (together with the São Luís cratonic fragment), in north-northeastern Brazil, has been described in previous studies that used extensive field geology, structural analysis, airborne geophysics, zircon U–Pb dating, and whole-rock Sm–Nd isotope and geochemical data as a polyphase orogenic belt, with the Rhyacian being the main period of crust formation. This was related to a 2240 Ma to 2140 Ma accretionary processes that produced juvenile crust, which has subsequently been reworked during a collisional event at 2100 ± 20 Ma, with little evidence of Archean crust. In this study, we use Lu–Hf isotopic data in zircon from granitoids (including gneiss) of variable magmatic series, and amphibolite to improve the knowledge of this scenario, and investigate additional evidence of recycling of Archean basement. Pre-collisional high Ba-Sr and ferroan granitoids and amphibolite formed in island arc (2180–2145 Ma), show only zircons with suprachondritic εHf values (ca. +1 to +8) indicating the large predominance of juvenile magmas. Only 10% of the data show slightly negative εHf values (0 to ?4), which have been observed in granodiorite-gneiss formed in continental arc (2170–2140 Ma), and in strongly peraluminous collisional granites (2125–2070 Ma), indicating the rework of older Paleoproterozoic to Archean components (Hf_TDM = 2.11–3.69 Ga). A two-component mixing model using both Hf and published Nd isotope data are in line with this interpretation and indicate more than 90% of juvenile material, and less influence of Archean materials. Comparing with other Rhyacian terranes that are interpreted to have been close to Gurupi in a pre-Columbia configuration (ca. 2.0 Ga), our results differ from those of SE-Guiana Shield, which show strong influence of Archean protoliths, and are very similar to those of the central-eastern portion of the Baoulé-Mossi Domain of the West African Craton, which has also been formed largely by juvenile magmas in an accretionary-collisional orogen.     

Genesis of the Maoling gold deposit in the Liaodong Peninsula: Constraints from a combined fluid inclusion,C-H-O-S-Pb-He-Ar isotopic and geochronological studies

The large tonnage Maoling gold deposit (25 t @ 3.2 g/t) is located in the southwest Liaodong Peninsula, North China Craton. The deposit is hosted in the Paleoproterozoic metamorphic rocks. Four stages of mineralization were identified in the deposit: (stage I) quartz-arsenopyrite ± pyrite, (stage II) quartz-gold- arsenopyrite-pyrrhotite, (stage III) quartz-gold- polymetallic sulfide, and (stage IV) quartz-calcite-pyrrhotite. In this paper, we present fluid inclusion, C-H-O-S-Pb-He-Ar isotope data, zircon U-Pb, and gold-bearing sulfide (i.e. arsenopyrite and pyrrhotite) Rb-Sr age of the Maoling gold deposit to constrain its genesis and ore-forming mechanism. Three types of fluid inclusions were distinguished in quartz-bearing veins, including liquid-rich two-phase (WL type), gas-rich two-phase (GL type), and daughter mineral-bearing fluid inclusions (S type). Fluid inclusions data show that the homogenization at temperatures 197 to 372 °C for stage I, 126 to 319 °C for stage II, 119 to 189 °C for stage III, and 115 to 183 °C for stage IV, with corresponding salinities of 3.7 to 22.6 wt.%, 4.7 to 23.2 wt.%, 5.3 to 23.2 wt.%, and 1.7 to 14.9 wt.% NaCl equiv., respectively. Fluid boiling was the critical factor controlling the gold and associated sulfide precipitation at Maoling. Hydrogen and oxygen stable isotopic analyses for quartz yielded δ¹⁸O = ?5.0‰ to 9.8‰ and δ D = ?133.5‰ to ?77.0‰. Carbon stable isotopic analyses for calcite and ankerite yielded δ¹³C = ?2.3‰ to ?1.2‰ and O = 7.9‰ to 14.1‰. The C-H-O isotope data show that the ore-forming fluids were originated from magmatic water with meteoric water input during mineralization. Hydrothermal inclusions in arsenopyrite have ³He/⁴He ratios of 0.002 Ra to 0.054 Ra, and ⁴⁰Ar/³⁶Ar rations of 1225 to 3930, indicating that the ore-forming fluids were dominantly derived from crustal sources almost no mantle input. Sulfur isotopic values of Maoling fine-grained granite range from 6.‰1 to 9.8‰, with a mean of 7.7‰, δ³⁴S values of arsenopyrite from the mineralized phyllite (host rock) range from 8.9‰ to 10.6‰, with a mean of 10.0‰, by contrast, δ³⁴S values of sulfides from ore vary between 4.3‰ and 10.6‰, with a mean of 6.8‰, suggesting that sulfur was mainly originated from both the host rock and magma. Lead radioactive isotopic analyses for sulfides yielded ²⁰⁶Pb/²⁰⁴Pb = 15.830–17.103, ²⁰⁷Pb/²⁰⁴Pb = 13.397–15.548, ²⁰⁸Pb/²⁰⁴Pb = 35.478–36.683, and for Maoling fine-grained granite yielded ²⁰⁶Pb/²⁰⁴Pb = 18.757–19.053, ²⁰⁷Pb/²⁰⁴Pb = 15.596–15.612, and ²⁰⁸Pb/²⁰⁴Pb = 38.184–39.309, also suggesting that the ore-forming materials were mainly originated from the host rocks and magma. Zircon U-Pb dating demonstrates that the Maoling fine-grained granite was emplaced at 192.7 ± 1.8 Ma, and the host rock (mineralized phyllite) was emplaced at some time after 2065.0 ± 27.0 Ma. Arsenopyrite and pyrrhotite give Rb–Sr isochron age of 188.7 ± 4.5 Ma, indicating that both magmatism and mineralization occurred during the Early Jurassic. Geochronological and geochemical data, together with the regional geological history, indicate that Early Jurassic magmatism and mineralization of the Maoling gold deposit occurred during the subducting Paleo-Pacific Plate beneath Eurasia, and the Maoling gold deposit is of the intrusion-related gold deposit type.     

δ34S isotope values of dissolved sulfate (SO4 2−) as a tracer for battery acid (H2SO4) contamination in groundwater

The application of sulfur isotope (³⁴S) values of sulfate in groundwater provided the information necessary to evaluate the source, transport and fate of battery acid and associated contaminants at the Gulf Coast Recycling (GCR) facility. The chemical and isotopic composition of groundwater beneath the (GCR) property, a battery recycling facility in east Tampa, Florida, varies more than expected for an area of comparable size. Sulfate (SO₄^2–) values, for example, range from 1.2 to 11,500 mg/L and oxygen and hydrogen isotopes do not attenuate towards the weighted annual mean. Those samples that are high in sulfate generally have a low pH, which immediately indicates battery acid (H₂SO₄) contamination as a potential source for the sulfate. The low pH and high reactivity of the sulfuric acid groundwater cause the formation of hydrogeological microenvironments due to preferential dissolution of carbonate minerals, which in turn causes enhanced recharge and groundwater flow in certain areas; thus, the extreme scatter in the data set. Because of the difficult hydrogeology it is not straightforward to delineate the point-sources of contamination and up to five potential scenarios have to be evaluated: (1) seawater intrusion, (2) upwelling of high-sulfate groundwater, (3) local dissolution of gypsum, (4) an up-gradient contaminant source to the northeast of the GCR property and (5) battery acid contamination.     

青海东昆仑造山型金（锑）矿床成矿流体地球化学研究

青海东昆仑是我国重要的、极富潜力的金属成矿带,其中产出的金矿床不仅具有相似的地质特征,而且与本区晚华力西-印支期造山过程有密切的成因联系,并在产出构造背景、矿体特征、控矿构造、围岩蚀变、矿物组成和元素组合等方面与一般造山型金矿床极为相似,因此应属典型的造山型金矿床.矿床流体包裹体十分发育,包括富CO2、CO2-H2O和H2O-NaCl三种类型,显微测温结果显示,成矿流体为一套中低温(120～380℃)、低盐度(0.35～9.54wt%NaCl)的H2O-CO2-NaCl-CH4±N2流体体系.氢、氧、碳同位素及水-岩交换反应研究表明,成矿流体早期主要为变质水和地层建造水,成矿期以来以大气降水为主.流体不混溶、大气降水的不断加入以及水-岩交换作用是导致本区成矿流体中金、锑淀积成矿的主要因素.