Pb–Pb Age of Carbonate Rocks of the Kamo Group,Baikit Anteclise of the Siberian Platform

Doklady Earth Sciences - The first direct Pb–Pb dating of carbonate rocks of the Kamo Group has been carried out. The Pb–Pb age of carbonates of the lower units (the Madra, Jurubchen,...     

S,Pb, and Sr isotope geochemistry and genesis of Pb–Zn mineralization in the Huangshaping polymetallic ore deposit of southern Hunan Province,China

The Huangshaping Pb–Zn–W–Mo polymetallic deposit, located in southern Hunan Province, China, is one of the largest deposits in the region and is unique for its metals combination of Pb–Zn–W–Mo and the occurrence of significant reserves of all these metals. The deposit contains disseminated scheelite and molybdenite within a skarn zone located between Jurassic granitoids and Carboniferous sedimentary carbonate, and sulfide ores located within distal carbonate-hosted stratiform orebodies. The metals and fluids that formed the W–Mo mineralization were derived from granitoids, as indicated by their close spatial and temporal relationships. However, the source of the Pb–Zn mineralization in this deposit remains controversial.Here, we present new sulfur, lead, and strontium isotope data of sulfide minerals (pyrrhotite, sphalerite, galena, and pyrite) from the Pb–Zn mineralization within the deposit, and these data are compared with those of granitoids and sedimentary carbonate in the Huangshaping deposit, thereby providing insights into the genesis of the Pb–Zn mineralization. These data indicate that the sulfide ores from deep levels in the Huangshaping deposit have lower and more consistent δ³⁴S values (− 96 m level: + 4.4‰ to + 6.6‰, n = 13) than sulfides within the shallow part of the deposit (20 m level: + 8.3‰ to + 16.3‰, n = 19). The δ³⁴S values of deep sulfides are compositionally similar to those of magmatic sulfur within southern Hunan Province, whereas the shallower sulfides most likely contain reduced sulfur derived from evaporite sediments. The sulfide ores in the Huangshaping deposit have initial ⁸⁷Sr/⁸⁶Sr ratios (0.707662–0.709846) that lie between the values of granitoids (0.709654–0.718271) and sedimentary carbonate (0.707484–0.708034) in the Huangshaping deposit, but the ratios decreased with time, indicating that the ore-forming fluids were a combination of magmatic and formation-derived fluids, with the influence of the latter increasing over time. The lead isotopic compositions of sulfide ores do not correlate with sulfide type and define a linear trend in a ²⁰⁷Pb/²⁰⁴Pb vs. ²⁰⁶Pb/²⁰⁴Pb diagram that is distinct from the composition of the disseminated pyrite within sedimentary carbonates and granitoids in the Huangshaping deposit, but is similar to the lead isotopic composition of sulfides within coeval skarn Pb–Zn deposits in southern Hunan Province. In addition, the sulfide ores have old signatures with relative high ²⁰⁷Pb/²⁰⁶Pb ratios, suggesting that the underlying Paleoproterozoic basement within southern Hunan Province may be the source of metals within the Huangshaping deposit.The isotope geochemistry of sulfide ores in the Huangshaping deposit shows a remarkable mixed source of sulfur and ore-forming fluids, and the metals were derived from the basement. These features are not found in representative skarn-type Pb–Zn mineralization located elsewhere. The ore-forming elements (S, Pb, and Zn) from the granitoids made an insignificant contribution to sulfide precipitation in this deposit. However, the emplacement of granitoids did provide large amounts of heat and fluids to the hydrothermal system in this area and extracted metals from the basement rocks, indicating that the Jurassic magmatism associated with the Huangshaping deposit was crucial to the Pb–Zn mineralization.     

Metallogenic Mechanism of the Tianbaoshan Pb—Zn Deposit,Sichuan

The Tianbaoshan Pb-Zn deposit in Sichuan Province,exhibiting open-space-filling and /or replacement textures,occurs as being of vine style in the Sinian(Late Proterozoic) carbonate rocks,and is simple in ore composition.A systematic study of lead isotope and rareearth elements reveals that the ore-forming materials were derived from multiple sources.The ultimate source of the sulfur in all stages in seawater sulfate but the reducing mechanisms are different,The carbon was derved from marine carbonate and organic matter,The ore-forming fluid,meteoric in origin,belongs to a Ca^2 -Mg^2 -Cl^--Hco3^- type of weak acidic to alkalic solutions with a salinity of about 5wt% NaCl.The ore was formed at the depth of about 1 km from 150 to 250℃ during the main stage of ore deposition.The heated meteoric water,after extracting ore materials from wall rocks,evolved into ore-forming solution with a low salinity, in which metals were trasported as chloride complexes such as PbCl,ZnCl and ZnCl.The metal-bearing solution moved upward along deep faults to low-pressure zones,where the metal ions reacted with reduced sulfur and were precipitated as sulfied minerals.The textures of the minerals were controlled by the rate at which the reduced sulfur was supplied.     

SHRIMP U–Pb zircon dating of the host rocks of the Cannington Ag–Pb–Zn deposit,southeastern Mt Isa Block,Australia

SHRIMP U–Pb zircon ages are reported from a paragneiss, a pegmatite, a metasomatised metasediment and an amphibolite taken from the upper amphibolite facies host sequence of the Cannington Ag–Pb–Zn deposit at the southeastern margin of the Proterozoic Mt Isa Block. Also reported are ages from a middle amphibolite‐facies metasediment from the Soldiers Cap Group approximately 90 km north of Cannington. The predominantly metasedimentary host rocks of the Cannington deposit were eroded from a terrane containing latest Archaean to earliest Palaeoproterozoic (ca 2600–2300 Ma) and Palaeoproterozoic (ca 1750–1700 Ma) zircon. The ca 1750–1700 Ma group of zircons are consistent with sedimentary provenance from rocks of Cover Sequence 2 age that are now exposed to the north and west of the Cannington deposit. The metasedimentary samples also include a group of zircon grains at ca 1675 Ma, which we interpret as the maximum depositional age of the sedimentary protolith. This is comparable to the maximum depositional age of the metasediment from the Maronan area (ca 1665 Ma) and to previously published data from the Soldiers Cap Group. Metamorphic zircon rims and new zircon grains grew at 1600–1580 Ma during upper amphibolite‐facies metamorphism in metasedimentary and mafic magmatic rocks. Zircon inheritance patterns suggest that sheet‐like pegmatitic intrusions were most likely derived from partial melting of the surrounding metasediments during this period of metamorphism. Some zircon grains from the amphibolite have a morphology consistent with partially recrystallised igneous grains and have apparent ages close to the metamorphic age, although it is not clear whether these represent metamorphic resetting or crystallisation of the magmatic protolith. Pb‐loss during syn‐ to post‐metamorphic metasomatism resulted in partial resetting of zircons from the metasomatised metasediment.     

U–Pb geochronology and Pb isotope characteristics of the Chahgaz volcanogenic massive sulphide deposit,southern Iran

The Chahgaz Zn–Pb–Cu volcanogenic massive sulphide (VMS) deposit occurs within a metamorphosed bimodal volcano–sedimentary sequence in the south Sanandaj–Sirjan Zone (SSZ) of southern Iran. This deposit is hosted by rhyodacitic volcaniclastics and is underlain and overlain by rhyodacitic flows, volcaniclastics, and pelites. Peperitic textures between rhyodacite flows and contact pelites indicate that emplacement of the rhyodacite occurred prior to the lithification of the pelites. The rhyodacitic flows are calc-alkaline, and show rare earth and trace elements features characteristic of arc magmatism. Zircons extracted from stratigraphic footwall and hanging-wall rhyodacitic flows of the Chahgaz deposit yield concordant U–Pb ages of 175.7 ± 1.7 and 172.9 ± 1.4 Ma, respectively, and a mean age of 174 ± 1.2 Ma. This time period is interpreted to represent the age of mineralization of the Chahgaz deposit. This Middle Jurassic age is suggested as a major time of VMS mineralization within pull-apart basins formed during Neo-Tethyan oblique subduction-related arc volcano-plutonism in the SSZ. Galena mineral separates from the layered massive sulphide have uniform lead isotope ratios of ²⁰⁶Pb/²⁰⁴Pb?=?18.604–18.617, ²⁰⁷Pb/²⁰⁴Pb?=?15.654–15.667, and ²⁰⁸Pb/²⁰⁴Pb?=?38.736–38.769; they show a model age of 200 Ma, consistent with the derivation of Pb from a Late Triassic, homogeneous upper crustal source.     

The geological significance of Pb–Bi- and Pb–Sb-sulphosalts in the Damajianshan tungsten polymetallic deposit,Yunnan Province,China

The Sanjiang Tethyan domain in SE Asia is one of the most important mineral belts in China. Cu, Pb–Zn, Ag, Au and Sn are the most important resources in this domain, while the tungsten mineralization is poorly reported. In this study, we report on mineralogy in recent discovered Damajianshan (DMJS) tungsten (–Cu–As–Mo–Bi) polymetallic deposit in the southern part of Sanjiang Tethyan domain related to Triassic quartz porphyry. Studies have shown that besides common ore minerals, such as native bismuth, bismuthinite, ikunolite, some specific minerals of Pb–Bi- and Pb–Sb-sulphosalts (e.g. izoklakeite, bournonite, cosalite, and boulangerite) have also been found. Based on paragenetic mineral assemblages, fluid inclusions, and thermodynamic studies, the physicochemical conditions were evaluated for the entire metallogenic process. The sulfur fugacity (logf_S2) ranges from − 9.7 to − 37 with ore-forming temperatures between 190 °C and 330 °C, and the oxygen fugacity (logf_O2) ranges from − 37.5 to − 38.5 when the temperature is 250 °C. The sulfur fugacity and oxygen fugacity show strong fluctuations with broadly negative correlation, indicating that these variations in physicochemical conditions should be responsible for mineral assemblages, and are one of the most significant factors leading to the formation of the DMJS deposit. Our mineralogical studies provide new information for tungsten mineralization and further exploration of tungsten resources in the Sanjiang Tethyan mineralization domain.     

Pb—Pb Age of the Bakal Ore Field Riphean Magnesite

For the first time, the age of magnesite in the Lower Riphean Bakal Formation of the Southern Urals is determined by the U—Pb (Pb—Pb) method: it is equal to 1366 ± 47 Ma (MSWD = 18). The stage of magnesite formation of the Bakal ore field was associated with the Mashak rifting pulse and took place prior to the formation of industrial deposits of the Bakal siderite.     

Early Archean crustal evolution of the Jack Hills Zircon source terrane inferred from Lu-Hf, Pb/Pb, and δO systematics of Jack Hills zircons

Several lines of isotopic evidence - the most direct of which is from Hadean Jack Hills zircons - suggest a very early history of crust formation on Earth that began by about 4.5 Ga. To constrain both the fate of the reservoir for this crust and the nature of crustal evolution in the sediment source region of the Jack Hills, Western Australia, during the early Archean, we report here initial ¹⁷⁶Hf/¹⁷⁷Hf ratios and δ¹⁸O systematics for <4 Ga Jack Hills zircons. In contrast to the significant number of Hadean zircons which contain highly unradiogenic ¹⁷⁶Hf/¹⁷⁷Hf requiring a near-zero Lu/Hf reservoir to have separated from the Earth’s mantle by 4.5 Ga, Jack Hills zircons younger than ca. 3.6 Ga are more radiogenic than -13ε (CHUR) at 3.4 Ga in contrast to projected values at 3.4 Ga of -20ε for the unradiogenic Hadean reservoir indicating that some later juvenile addition to the crust is required to explain the more radiogenic younger zircons. The shift in the Lu-Hf systematics together with a narrow range of mostly mantle-like δ¹⁸O values among the <3.6 Ga zircons (in contrast to the spread towards sedimentary δ¹⁸O among Hadean samples) suggests a period of transition between 3.6 and 4 Ga in which the magmatic setting of zircon formation changed and the highly unradiogenic low Lu/Hf Hadean crust ceased to be available for intracrustal reworking. Constraining the nature of this transition provides important insights into the processes of crustal reworking and recycling of the Earth’s Hadean crust as well as early Archean crustal evolution.     

Trace element signature and U–Pb geochronology of eclogite-facies zircon,Bergen Arcs,Caledonides of W Norway

Secondary-ion mass spectrometry (SIMS) U–Pb and trace element data are reported for zircon to address the controversial geochronology of eclogite-facies metamorphism in the Lindås nappe, Bergen Arcs, Caledonides of W Norway. Caledonian eclogite-facies overprint in the nappe was controlled by fracturing and introduction of fluid in the Proterozoic—Sveconorwegian—granulite-facies meta-anorthosite-norite protolith. Zircon grains in one massive eclogite display a core–rim structure. Sveconorwegian cores have trace element signatures identical with those of zircon in the granulite protolith, i.e. 0.31Th/U0.89, heavy rare earth element (HREE) enrichment, and negative Eu anomaly. Weakly-zoned to euhedral oscillatory-zoned Caledonian rims are characterized by Th/U0.13, low LREE content (minimum normalized abundance for Pr or Nd), variable enrichment in HREE, and no Eu anomaly. A decrease of REE towards the outermost rim, especially HREE, is documented. This signature reflects co-precipitation of zircon with garnet and clinozoisite in a feldspar-absent assemblage, and consequently links zircon to the eclogite-facies overprint. The rims provide a mean ²⁰⁶Pb/²³⁸U crystallization age of 423±4 Ma. This age reflects eclogite-forming reactions and fluid–rock interaction. This age indicates that eclogite-facies overprint in the Lindås nappe took place at the onset of the Scandian (Silurian) collision between Laurentia and Baltica.     

Isotopic (Sr, Nd, Pb) characteristics of the archean metasomatized mantle—source of the Panozero massif, Karelia

This work addresses the isotopic heterogeneity of the Archean lithospheric mantle by the example of high-Mg, moderate-alkali, LILE and LREE-enriched Panozero sanukitoid massif, which is located in the Central Karelia, southeastern Baltic Shield. Initial Nd and Sr isotope characteristics were determined for mantle source of the massif. ?_Nd(T) in the source are plotted below DM line, varying from + 0.7 to + 1.4 (+1.1, on average). The ⁸⁷Sr/⁸⁶Sr(T) ～ 0.7017 significantly exceeds that of depleted mantle and reflects change of Rb/Sr ratio in the source due to metasomatic reworking of mantle. Data on Pb isotope composition of potassium feldspars indicate that source of monzonites of the Panozero Massif had lower μ (²³⁸U/²⁰⁴Pb) = 8 and higher (²³⁸Th/²³²U) = 4.05 relative to primitive mantle.     

U–Pb and Th–Pb dating of apatite by LA-ICPMS

Apatite is a common U- and Th-bearing accessory mineral in igneous and metamorphic rocks, and a minor but widespread detrital component in clastic sedimentary rocks. U–Pb and Th–Pb dating of apatite has potential application in sedimentary provenance studies, as it likely represents first cycle detritus compared to the polycyclic behavior of zircon. However, low U, Th and radiogenic Pb concentrations, elevated common Pb and the lack of a U–Th–Pb apatite standard remain significant challenges in dating apatite by LA-ICPMS, and consequently in developing the chronometer as a provenance tool.This study has determined U–Pb and Th–Pb ages for seven well known apatite occurrences (Durango, Emerald Lake, Kovdor, Mineville, Mud Tank, Otter Lake and Slyudyanka) by LA-ICPMS. Analytical procedures involved rastering a 10 μm spot over a 40 × 40 μm square to a depth of 10 μm using a Geolas 193 nm ArF excimer laser coupled to a Thermo ElementXR single-collector ICPMS. These raster conditions minimized laser-induced inter-element fractionation, which was corrected for using the back-calculated intercept of the time-resolved signal. A Tl–U–Bi–Np tracer solution was aspirated with the sample into the plasma to correct for instrument mass bias. External standards (Ple?ovice and 91500 zircon, NIST SRM 610 and 612 silicate glasses and STDP5 phosphate glass) along with Kovdor apatite were analyzed to monitor U–Pb, Th–Pb, U–Th and Pb–Pb ratiosCommon Pb correction employed the ²⁰⁷Pb method, and also a ²⁰⁸Pb correction method for samples with low Th/U. The ²⁰⁷Pb and ²⁰⁸Pb corrections employed either the initial Pb isotopic composition or the Stacey and Kramers model and propagated conservative uncertainties in the initial Pb isotopic composition. Common Pb correction using the Stacey and Kramers (1975) model employed an initial Pb isotopic composition calculated from either the estimated U–Pb age of the sample or an iterative approach. The age difference between these two methods is typically less than 2%, suggesting that the iterative approach works well for samples where there are no constraints on the initial Pb composition, such as a detrital sample. No ²⁰⁴Pb correction was undertaken because of low ²⁰⁴Pb counts on single collector instruments and ²⁰⁴Pb interference by ²⁰⁴Hg in the argon gas supply.Age calculations employed between 11 and 33 analyses per sample and used a weighted average of the common Pb-corrected ages, a Tera–Wasserburg Concordia intercept age and a Tera–Wasserburg Concordia intercept age anchored through common Pb. The samples in general yield ages consistent (at the 2σ level) with independent estimates of the U–Pb apatite age, which demonstrates the suitability of the analytical protocol employed. Weighted mean age uncertainties are as low as 1–2% for U- and/or Th-rich Palaeozoic–Neoproterozoic samples; the uncertainty on the youngest sample, the Cenozoic (31.44 Ma) Durango apatite, ranges from 3.7–7.6% according to the common Pb correction method employed. The accurate and relatively precise common Pb-corrected ages demonstrate the U–Pb and Th–Pb apatite chronometers are suitable as sedimentary provenance tools. The Kovdor carbonatite apatite is recommended as a potential U–Pb and Th–Pb apatite standard as it yields precise and reproducible ²⁰⁷Pb-corrected, ²³²Th–²⁰⁸Pb, and common Pb-anchored Tera–Wasserburg Concordia intercept ages.     

Sources of pollution and distribution of Pb,Cd and Hg in Wrocław soils: Insight from chemical and Pb isotope composition

Human activities in cities affect properties of urban soils. In particular, urban soils often contain high contents of harmful metals even in deeper horizons added to them from diverse sources over centuries of the city development. This is reflected in complex distribution of metals in bulk soils with depth and the complex metal fractionation, but the exact sources of the metals are difficult to identify. This is also the situation in soils from Wroclaw, one of the largest cities in Poland. Potentially harmful elements Pb, Cd and Hg were examined in six profiles located along the major communication route and compared to two non-urban soils profiles located close to the same route. In all of the urban profiles, Pb and Cd exceeded the element contents observed in non-urban profiles and showed an erratic distribution compared to the more predictable one in non-urban soils. The differences between urban and non-urban profiles were explained as the result of contamination coming from more pollution sources in the case of urban soils, the conclusion supported by Pb isotope analyses. In fact, Pb isotopes showed that the contamination sources in urban soils included leaded petrol, coal combustion, smelting and possibly old pre-industrial ore processing, whereas leaded petrol and pre-industrial lead were the only possible anthropogenic sources in non-urban soils. The comparison of Wrocöaw soils with those from cities of comparable size Kraków and Poznań show similar ranges of metal contents with implication that urban pollution oversteps diverse geogenic chemical background. On the other hand, the comparison with other European cities show large variability in metal contents and suggest that urban soils contamination is time integrated and reflects long-term industrial evolution of each country.     

U—Pb Dating of Anatectic Migmatites in the Yunkai Block,Gaozhou,Western Guangdong

The regional migmatites in the Yunkai Block were formed under low-pressure metamorphism.The majority of their protolith are biotite-rich peraluminous gneisses.Detailed field observations,and studies of petrology,spatial distribution of minerals and geochemistry suggest that the leucosomes were derived from anatexis.The single grain zircon U-Pb dating data indicate that a pulse of migmatization occurred at 394-449 Ma and may have resulted from the large-scale Caledonian magmatism in the Yunkai Block.     

Geochemistry and zircon U–Pb geochronology of the Pulang complex,Yunnan province,China

The Pulang complex is located tectonically at the southern margin of the Yidun–Zhongdian island arc belt in Yunnan province, China, and is closely related to formation of the Pulang copper deposit, which is the largest copper deposit in Asia. The Pulang complex can be divided into three intrusion stages based on contact relationships and petrological characteristics: (1) a first stage of quartz dioritic porphyry; (2) a second stage of quartz monzonitic porphyry; and (3) a third stage of granodioritic porphyry. The crystallization ages of these intrusion stages were determined by single-zircon U–Pb dating, yielding ages of 221.0 ± 1.0, 211.8 ± 0.5, and 206.3 ± 0.7 Ma for the first, second, and third stages, respectively. These dates, integrated with previous geochronological data and field investigations, indicate that the second-stage quartz monzonitic porphyry has a close spatial and temporal relationship with the large Pulang porphyry copper deposit. These age data, geochemical and Sr–Nd isotopic results suggest that the Pulang complex formed in the Indo-Chinese epoch (257 ～ 205 Ma) by multiphase intrusion of a mixture of mantle- and crust-derived magmas.     

Sr,Nd,Pb Isotope Geochemistry and Magma Evolution of the Potassic Volcanic Rocks,Wudalianchi,Northeast China

Wudalianchi volcanic rocks are the most typical Cenozoic potassic volcanic rocks in easten China.Compositional comparisons between whole rocks and glasses of various occurrences indicate that the magma tends to become rich in silica and alkalis as a result of crystal differentiation in the course of evolu-tion.They are unique in isotopic composition with more radiogenic Sr but less radiogenic Pb.^87Sr/^86Sr is higher and ^143Nd/^144Nd is lower than the undifferentiated global values.In comparison to continental pot-ash volcanic rocks,Pb isotopes are apparently lower.These various threads of evidence indicate that the rocks were derived from a primary enriched mantle which had not been subjected to reworking and shows no sign of incorporation of crustal material.The correlation between Pb and Sr suggests the regional heterogeneity in the upper mantle in terms of chemical composition.     

Zircon U–Pb dating of Pubei granite and strontium isotope from sphalerite of the Xinhua Pb–Zn–(Ag) deposit,Yunkai Area of Guangxi Province,South China

The Yunkai Area is located at the southern South China Block and is part of the Qinzhou Bay-Hangzhou Bay Metallogenic Belt, which is a famous polymetallic mineralization belt. The Xinhua Pb–Zn–(Ag) deposit is located in the western part of Yunkai Area, with an abundance of Pubei batholiths. Zircon U–Pb geochronology of Pubei batholiths shows that crystallization age ranges from 251.9 ± 2.2 to 244.3 ± 1.8 Ma, thus belonging to Indosinian orogeny. Geochemistry and Sr isotopic compositions of the Pubei batholiths show that it is derived from the partial melting of large scale crustal melting during the stage of exhumation and uplifting of the lower-middle crust. In addition, strontium isotope of sphalerite from the Xinhua Pb–Zn–(Ag) deposit, has limited ranges in ⁸⁷Rb/⁸⁶Sr and ⁸⁷Sr/⁸⁶Sr, ranging from 0.4077 to 1.0449, and 0.718720 to 0.725245, respectively. The initial ⁸⁷Sr/⁸⁶Sr ratios of sphalerite ranges between 0.718720 and 0.725245, which is higher than that of upper continental crust and lower than that of the Pubei batholiths, illustrating the fluid might be derived from the mixing of Pubei pluton and upper continental crust.     

Metallogeny of precious and base metal mineralization in the Murchison Greenstone Belt, South Africa: indications from U–Pb and Pb–Pb geochronology

The 3.09 to 2.97 Ga Murchison Greenstone Belt is an important metallotect in the northern Kaapvaal Craton (South Africa), hosting several precious and base metal deposits. Central to the metallotect is the Antimony Line, striking ENE for over 35?km, which hosts a series of structurally controlled Sb–Au deposits. To the north of the Antimony Line, hosted within felsic volcanic rocks, is the Copper–Zinc Line where a series of small, ca. 2.97 Ga Cu–Zn volcanogenic massive sulfide (VMS)-type deposits occur. New data are provided for the Malati Pump gold mine, located at the eastern end of the Antimony Line. Crystallizations of a granodiorite in the Malati Pump Mine and of the Baderoukwe granodiorite are dated at 2,964?±?7 and 2,970?±?7?Ma, respectively (zircon U–Pb), while pyrite associated with gold mineralization yielded a Pb–Pb age of 2,967?±?48?Ma. Therefore, granodiorite emplacement, sulfide mineral deposition and gold mineralization all happened at ca. 2.97?Ga. It is, thus, suggested that the major styles of orogenic Au–Sb and the Cu–Zn VMS mineralization in the Murchison Greenstone Belt are contemporaneous and that the formation of meso- to epithermal Au–Sb mineralization at fairly shallow levels was accompanied by submarine extrusion of felsic volcanic rocks to form associated Cu–Zn VMS mineralization.