scholarly journals Geology, Mineralogy, Fluid Inclusion, and H–O–S–Pb Isotope Constraints on Ore Genesis of the Keyue Sb–Pb–Zn–Ag Deposit in Southern Tibet

Geofluids ◽  
2018 ◽  
Vol 2018 ◽  
pp. 1-32 ◽  
Author(s):  
Da Wang ◽  
Youye Zheng ◽  
Wantao Yang ◽  
Ngawang Gyatso

The Keyue deposit is a medium-sized deposit similar to the Zhaxikang deposit within the North Himalayan Metallogenic Belt (NHMB). The ore formation can be divided into Pb–Zn mineralization (stages 1 and 2), Sb–Ag mineralization (stages 3 and 4), and Sb–Hg mineralization (stages 5 and 6). The fluid inclusion data show that the first two pulses of mineralization have different characteristics, but both belong to the epithermal category (stage 2: 172.9~277.2°C, 7.4~17.0 wt% NaCl eq.; stages 3 and 4: 142.1~321.0°C, 2.7~17.96 wt% NaCl eq.). The H–O isotopic compositions of stages 3 and 4 quartz (δDV-SMOW: –174‰~−120‰, δ18OH2O: 1.59‰~11.34‰) are similar to those of stages 3 and 4 minerals (δDV-SMOW: –165‰~−150‰, δ18OH2O: 6.14‰~13.03‰), whereas they are different from stage 1 and 2 (δDV-SMOW: –108.3‰~−103.6‰, δ18OH2O: 1.92‰~3.82‰) and stage 5 and 6 (δDV-SMOW: –165‰~−138‰, δ18OH2O: −12.91‰~0.82‰) minerals from the Zhaxikang deposit. Additionally, stage 2 sulfides have δ34S values of 5.4‰~11.2‰ that are similar to stage 2 sulfides in the Zhaxikang deposit (7.8‰~12.2‰), and these δ34S values overlap those of many SEDEX-type deposits. The δ34S values also show a decreasing trend from stage 2 through stages 3 and 4 to stage 5 in Keyue and Zhaxikang deposits, which may relate to the overprint by later mineralization events. The Pb isotopic data (206Pb/204Pb: 18.530~19.780, 207Pb/204Pb: 15.674~15.939, and 208Pb/204Pb: 38.618~40.559) show a significant crustal contribution. However, the minerals from different pulses of mineralization also exhibit slightly different Pb isotopic characteristics. These inferences from fluid inclusions and isotope are also demonstrated by geological and mineralogical evidence. Overall, the Keyue deposit is an epithermal deposit and has mainly experienced three pulses of mineralization.

Minerals ◽  
2018 ◽  
Vol 8 (10) ◽  
pp. 448 ◽  
Author(s):  
Shun-Da Li ◽  
Zhi-Gao Wang ◽  
Ke-Yong Wang ◽  
Wen-Yan Cai ◽  
Da-Wei Peng ◽  
...  

The Jinchang gold deposit is located in the eastern Yanji–Dongning Metallogenic Belt in Northeast China. The orebodies of the deposit are hosted within granite, diorite, and granodiorite, and are associated with gold-mineralized breccia pipes, disseminated gold in ores, and fault-controlled gold-bearing veins. Three paragenetic stages were identified: (1) early quartz–pyrite–arsenopyrite (stage 1); (2) quartz–pyrite–chalcopyrite (stage 2); and (3) late quartz–pyrite–galena–sphalerite (stage 3). Gold is hosted predominantly within pyrite. Pyrite separated from quartz–pyrite–arsenopyrite cement within the breccia-hosted ores (Py1) yield a Re–Os isochron age of 102.9 ± 2.7 Ma (MSWD = 0.17). Pyrite crystals from the quartz–pyrite–chalcopyrite veinlets (Py2) yield a Re–Os isochron age of 102.0 ± 3.4 Ma (MSWD = 0.2). Pyrite separated from quartz–pyrite–galena–sphalerite veins (Py3) yield a Re–Os isochron age of 100.9 ± 3.1 Ma (MSWD = 0.019). Re–Os isotopic analyses of the three types of auriferous pyrite suggest that gold mineralization in the Jinchang Deposit occurred at 105.6–97.8 Ma (includes uncertainty). The initial 187Os/188Os values of the pyrites range between 0.04 and 0.60, suggesting that Os in the pyrite crystals was derived from both crust and mantle sources.


2021 ◽  
Vol 32 (1) ◽  
pp. 103-115
Author(s):  
Fan Yang ◽  
Xuejiao Pang ◽  
Bin Li ◽  
Jingsheng Chen ◽  
Jilong Han ◽  
...  

Atmosphere ◽  
2021 ◽  
Vol 12 (3) ◽  
pp. 388
Author(s):  
Andrea Bazzano ◽  
Stefano Bertinetti ◽  
Francisco Ardini ◽  
David Cappelletti ◽  
Marco Grotti

Lead content, enrichment factors, and isotopic composition (208Pb/206Pb and 207Pb/206Pb) measured in atmospheric particulate matter (PM10) samples collected for nine years at Ny-Ålesund (Svalbard islands, Norwegian Arctic) during spring and summer are presented and discussed. The possible source areas (PSA) for particulate inferred from Pb isotope ratio values were compared to cluster analysis of back-trajectories. Results show that anthropogenic Pb dominates over natural crustal Pb, with a recurring higher influence in spring, compared to summer. Crustal Pb accounted for 5–16% of the measured Pb concentration. Anthropogenic Pb was affected by (i) a Central Asian PSA with Pb isotope signature compatible with ores smelted in the Rudny Altai region, at the Russian and Kazakhstan border, which accounted for 85% of the anthropogenic Pb concentration, and (ii) a weaker North American PSA, contributing for the remaining 15%. Central Asian PSA exerted an influence on 71–86% of spring samples, without any significant interannual variation. On the contrary, 59–87% of summer samples were influenced by the North American PSA, with higher contributions during 2015 and 2018. Back-trajectory analysis agreed on the seasonal difference in PSA and highlighted a possible increased influence for North American air masses during summer 2010 and 2018, but not for summer 2015.


Minerals ◽  
2021 ◽  
Vol 11 (4) ◽  
pp. 354
Author(s):  
Anatoly M. Sazonov ◽  
Aleksei E. Romanovsky ◽  
Igor F. Gertner ◽  
Elena A. Zvyagina ◽  
Tatyana S. Krasnova ◽  
...  

The gold and platinum-group elements (PGE) mineralization of the Guli and Kresty intrusions was formed in the process of polyphase magmatism of the central type during the Permian and Triassic age. It is suggested that native osmium and iridium crystal nuclei were formed in the mantle at earlier high-temperature events of magma generation of the mantle substratum in the interval of 765–545 Ma and were brought by meimechite melts to the area of development of magmatic bodies. The pulsating magmatism of the later phases assisted in particle enlargement. Native gold was crystallized at a temperature of 415–200 °C at the hydrothermal-metasomatic stages of the meimechite, melilite, foidolite and carbonatite magmatism. The association of minerals of precious metals with oily, resinous and asphaltene bitumen testifies to the genetic relation of the mineralization to carbonaceous metasomatism. Identifying the carbonaceous gold and platinoid ore formation associated genetically with the parental formation of ultramafic, alkaline rocks and carbonatites is suggested.


Geofluids ◽  
2020 ◽  
Vol 2020 ◽  
pp. 1-21
Author(s):  
Xinglin Chen ◽  
Yongjun Shao ◽  
Chunkit Lai ◽  
Cheng Wang

The Longmendian Ag–Pb–Zn deposit is located in the southern margin of the North China Craton, and the mineralization occurs mainly in quartz veins, altered gneissic wallrocks, and minor fault breccias in the Taihua Group. Based on vein crosscutting relations, mineral assemblages, and paragenesis, the mineralization can be divided into three stages: (1) quartz–pyrite, (2) quartz–polymetallic sulfides, and (3) quartz–carbonate–polymetallic sulfides. Wallrock alteration can be divided into three zones, i.e., chlorite–sericite, quartz–carbonate–sericite, and silicate. Fluid inclusions in all Stage 1 to 3 quartz are dominated by vapor-liquid two-phase aqueous type (W-type). Petrographic and microthermometric analyses of the fluid inclusions indicate that the homogenization temperatures of Stages 1, 2, and 3 are 198–332°C, 132–260°C, and 97–166°C, with salinities of 4.0–13.3, 1.1–13.1, and 1.9–7.6 wt% NaCleqv, respectively. The vapor comprises primarily H2O, with some CO2, H2, CO, N2, and CH4. The liquid phase contains Ca2+, Na+, K+, SO42−, Cl−, and F−. The sulfides have δ34S=–1.42 to +2.35‰ and 208Pb/204Pb=37.771 to 38.795, 207Pb/204Pb=15.388 to 15.686, and 206Pb/204Pb=17.660 to 18.101. The H–C–O–S–Pb isotope compositions indicate that the ore-forming materials may have been derived from the Taihua Group and the granitic magma. The fluid boiling and cooling and mixing with meteoric water may have been critical for the Ag–Pb–Zn ore precipitation. Geological and geochemical characteristics of the Longmendian deposit indicate that the deposit is best classified as medium- to low-temperature intermediate-sulfidation (LS/IS) epithermal-type, related to Cretaceous crustal-extension-related granitic magmatism.


1984 ◽  
Vol 21 (1) ◽  
pp. 74-84 ◽  
Author(s):  
Hans Petter Sejrup ◽  
Eystein Jansen ◽  
Helmut Erlenkeuser ◽  
Hans Holtedahl

Downcore studies of planktonic and benthonic foraminifera and δ18O and δ13C in the planktonic foraminifer Neogloboquadrina pachyderma (sin.) in two piston cores from the southern part of the Norwegian Sea suggest large changes in the oceanic circulation pattern at the end of oxygenisotope stage 2 and in the early part of stage 1. Prior to oxygen-isotope Termination IA (16,000–13,000 yr B.P.), an isolated watermass with lower oxygen content and temperature warmer than today existed below a low salinity ice-covered surface layer in the Norwegian Sea. Close to Termination IA, well-oxygenated deep water, probably with positive temperatures, was introduced. This deep water, which must have had physical and/or chemical parameters different from those of present deep water in the Norwegian Sea, could have been introduced from the North Atlantic or been formed within the basin by another mechanism than that which forms the present deep water of the Norwegian Sea. A seasonal ice cover in the southern part of the Norwegian Sea is proposed for the period between Termination IA and the beginning of IB (close to 10,000 yr B.P.). The present situation, with strong influx of warm Atlantic surface-water and deep-water formation by surface cooling, was established at Termination IB.


Geofluids ◽  
2018 ◽  
Vol 2018 ◽  
pp. 1-25
Author(s):  
Lu Zhang ◽  
Shao-Yong Jiang ◽  
Suo-Fei Xiong ◽  
Deng-Fei Duan

The Fuzishan Cu-Mo deposit is located in the Edong district of the Middle-Lower Yangtze River Metallogenic Belt, China. The orebodies mainly occurred as lenticular and bedded shapes in the skarn zone between the Lower Permian Qixia Formation carbonate rocks and the quartz diorite. Four paragenetic stages have been recognized based on petrographic observations: (1) prograde skarn stage, (2) retrograde skarn stage, (3) quartz-sulfide stage, and (4) carbonate stage. Six fluid inclusion types were recognized: S1(vapor + liquid + halite ± other daughter minerals), S2(vapor + liquid + daughter minerals except halite), LV(rich liquid + vapor), VL(rich vapor + liquid), V (vapor), and L (liquid) types. Fluid inclusion studies show distinct variations in composition, final homogenization temperature, and salinity in four stages. Daughter minerals of the primary fluid inclusions include chalcopyrite, molybdenite, hematite, anhydrite, calcite, and halite in the prograde skarn stage and hematite, calcite, and sulfide (?) in the retrograde skarn stage. No daughter minerals occurred in the quartz-sulfide and carbonate stages. Final homogenization temperatures recorded in these stages are from 405 to >550°C, from 212 to 498°C, from 150 to 485°C, and from 89 to 223°C, respectively, while salinities are from 3.7 to 42.5, from 2.6 to 18.5, from 2.2 to 17.9, and from 0.2 to 11.5 wt.% NaCl equivalent, respectively. The coexisting VLand S1type fluid inclusions show similar homogenization temperature of 550 to about 650°C in the prograde skarn stage, indicating that immiscibility occurred at lithostatic pressure of 700 bars to perhaps 1000 bars, corresponding to a depth of 2.6 km to about 3.7 km. The coeval VLand LVtypes fluid inclusions with homogenization temperature of 350 to 400°C in the late retrograde skarn and quartz-sulfide stages suggest that boiling occurred under hydrostatic pressure of 150 to 280 bars, equivalent to a depth of 1.5 to 2.8 km. Mo mineralization in the retrograde stage predated Cu mineralization which mainly occurred in the quartz-sulfide stage. Fluid compositions indicate that ore-forming fluid has highfO2and rich Cu and Mo concentration in the early stage, while relatively lowerfO2and poor Cu and Mo concentration in the middle to late stages. Microthermometric data show a decreasing trend in temperature and salinity in the fluid evolution process. Decreasing temperature and boiling event may be the main factors that control the ore precipitation.


1981 ◽  
Vol 1 (1) ◽  
Author(s):  
A. H. G. Mitchell

Granitic rocks occupying eight distinct tectonic settings can be recognized in the Himalayas and   Transhimalayas.  In the Lower Himalayas geographical belt a few plutons of two-mica granite intrude the lowest unit of the Nawakot Complex or Midland Group. More extensive are sheet- like lies of augen gneiss intrusive within a possibly thrust bounded succession carbonates and graphitic schists beneath the Main Central Thrust to the north. The most abundant granites in the Lower Himalayas are the two- mica cordierite- bearing granite within klippen; minor tin and tungsten mineralization is associated with these plutons, which are of late Cambrian age. Within the Higher Himalayas above the Main Central Thrust, the ‘Central Crystallines’ or Central Gneisses include pegmatites and pegmatitic granites intrusive into gneisses of probable early Proterozoic age; these have same potential for ruby, sapphire, aquamarine and possibly spodumene. Further north within the Higher Himalayan succession a southern belt of anatectic two- mica granites and leucogranites of mid-Tertiary age is favorable for tin, tungsten and uranium mineralization; a northern belt of granites or gneisses is of uncertain age and origin. North of the Indus Suture in the Transhimalayas extensive batholiths of hornblende granodiorite representing the root zone of a late Mesozoic to early Eocene volcanic arc are associated with porphyry copper deposits. Further north in southern Tibet the tectonic, setting for reported granitic bodies of  Tertiary  age  is  uncertain; their location suggests that they could be favorable host rocks for tin, uranium and porphyry molybdenum mineralization.


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