NaCl Equiv Research Articles

Overlapping events in the Acoculco geothermal system, Puebla, Mexico

The Acoculco geothermal system records two major hydrothermal events (prograde skarn overlapped by retrograde/”epithermal” to geothermal stages) in association with pre-calderic to calderic events in the eponymous complex, which belongs to the Trans-Mexican Volcanic Belt. The prograde skarn is associated with a hornblende granite (hereby dated at 1.01 ± 0.01 Ma; U-Pb zircon age), whose apex is found at a ∼1600 m depth, and later andesite dykes and sills. Mineralizing fluids in this stage have salinities of fluid inclusions that range between 9.5 wt.% NaCl equiv. and 33 wt.% NaCl and temperatures of homogenization (Th) up to 470 °C that record various process of mineral formation, such as boiling, depressurization, conductive cooling, isothermal mixing, and dilution. The retrograde stage is represented by early “fossil” brines with salinities 1.4 and 7.3 wt.% NaCl equiv. and Th up to 303 °C, and present-day gasothermal fluids that attain stabilized temperatures up to ∼300 °C at a depth of almost 2000 m. Th of early brines are consistently higher than stabilized temperatures at most of the depths that were surveyed, the isotherms that correspond to 250° and 200 °C dropped ca. 500 m from the early retrograde to the gasothermal stage. These features support the hypothesis that the Acoculco geothermal system has entered its senile stage. Despite that, upon a calculated geothermal gradient at ∼150 °C/km for both Th of the early retrograde stage and stabilized temperatures in the EAC-1 well, it is not foreseen a rapid waning of the thermal anomaly and its ultimate cause.Besides the early Ca-silicate assemblages that constitute the skarn, the architecture of alteration assemblages also records the overlapping of shallow on deep hypogene assemblages. The deep hypogene assemblages respond to alkaline to moderately acidic fluids that correspond to the early retrograde (or “epithermal”) stage: propylitic, phyllic and argillic (kaolinite + nontronite + montmorillonite), from bottom to top. Contrastingly, the shallow hypogene assemblages respond to dominantly acidic fluids, and consist of advanced argillic assemblages that may grade upwards into argillic (kaolinite + illite-smectite) or silicic (vuggy or massive to brecciated silica). The shallow hypogene character of advanced argillic assemblages, as due to steam-heated ground environments (as opposed to deep hypogene or magmatic-hydrothermal assemblages), is deduced from (1) the overall tabular shape of their distribution, (2) the mineralogical association and characteristics of rhombohedral alunite within it, and (3) its relationship with overlying silicic alteration that, in turn, do not possess likely characteristics of sinters. Shallow hypogene advanced argillic assemblages are associated with the present-day gasothermal activity due to sealing that was possibly promoted during the early retrograde/”epithermal” activity.

Separation of Au and Sb mineralization in the Qukulekedong intrusion-related deposit, East Kunlun Orogen (NW China): Evidence from fluid inclusions, H–O isotopes, and quartz geochemistry

Separation of Au and Sb mineralization from different hydrothermal stages is a common phenomenon in many Au–Sb deposits, but its cause remains enigmatic. The Qukulekedong intrusion-related Au–Sb deposit in the East Kunlun Orogen has undergone four hydrothermal stages: (1) barren quartz vein, (2) quartz vein with disseminated arsenopyrite–pyrite alteration halo, (3) stibnite–quartz ± native gold vein, and (4) calcite–quartz vein. Stages 2 and 3 formed disseminated Au and vein-type Sb ± Au ore, respectively. Here, internal texture and trace elements in quartz, fluid inclusions (Fls) microthermometry, and H–O isotopes were analyzed to unravel the separation mechanism of the Au and Sb ± Au mineralization at Qukulekedong. Stage 2 quartz has euhedral growth zones with elevated Ti-Al-Li-K-Sb and varying As contents. Stage 2 FIs have medium homogenization temperature (203–307 °C) and salinity (12.2–17.8 wt% NaCl equiv.), and are CH4-rich. They have δ18OH2O = 9.5–10.8 ‰ and δDH2O = −93.4 to −80.8 ‰. In contrast, stage 3 quartz has lower Ti-Al-Li-K and varying Sb contents. Stage 3 FIs show phase separation (coexistence of V-, L- and V-L-type FIs), and are of lower temperature (141–164 °C) and salinity (2.1–10.7 wt% NaCl equiv.), and CO2– and CH4-bearing. They have δ18OH2O = 3.3–5.2 ‰ and δDH2O = − 95.4 to − 89.6 ‰. Considering that the disseminated Au ore is Sb-rich and its pyrite has fine stibnite inclusions, we suggest that the disseminated Au and vein-type Sb ± Au mineralization shared a common Au- and Sb-rich initial magmatic fluids. The disseminated Au mineralization may have formed by fluid–rock interactions. Meanwhile, the vein-type Sb ± Au mineralization was likely caused by the phase separation and cooling led by dilational activities and meteoric water injection.

Sulfur and Carbon–Oxygen Isotopic Geochemistry and Fluid Inclusion Characteristics of the Yolindi Cu-Fe Skarn Mineralization, Biga Peninsula, NW Turkey: Implications for the Source and Evolution of Hydrothermal Fluids

The current study sought to investigate the physiochemical conditions and fluid evolution within the Yolindi Cu-Fe skarn mineralization located in the Biga Peninsula, NW Turkey. This was accomplished through a comprehensive investigation of geological and mineralogical data, along with isotopic analyses of sulfur (δ34S), carbon (δ13C), and oxygen (δ18O) of sulfide and calcite minerals, respectively, as well as fluid inclusion data pertaining to various minerals (e.g., andradite, quartz, and calcite). The Yolindi area features a complex geological framework, including the Paleozoic Kalabak Group (which includes the Torasan, Yolindi, and Sazak formations) and the Triassic Karakaya Complex. These formations were subsequently intruded via Early Miocene Şaroluk granitoids and Hallaçlar volcanics. Skarn formation is zoned into endoskarn and exoskarn types (being categorized into proximal, intermediate, and distal zones), with distinct mineral assemblages indicating concentric and contact metamorphic alteration patterns around the western part of Şaroluk granitoid intrusion in contact with the Torasan formation. The ore mineralogy and paragenesis suggest three distinct stages of evolution: an initial phase of prograde metasomatism characterized by the formation of magnetite and pyrite alongside anhydrous calc-silicate minerals; a subsequent phase of retrograde alteration marked by the formation of epidote, actinolite, and scapolite, accompanied by the occurrence of chalcopyrite and specular hematite; and finally, a post-metasomatic stage involving oxidation processes that led to the development of secondary mineral assemblages containing cerussite, covellite, and malachite. Sulfur isotopes (δ34S) of sulfides from endoskarn (from +0.27 to +0.57‰VCDT) to intermediate exoskarn (from −9.44 to −5.46‰VCDT) zones indicate a diverse sulfur source, including magmatic, sedimentary, and possibly organic matter. δ34S values in hydrothermal fluids suggest a magmatic–hydrothermal origin, with endoskarn and proximal zone fluids showing a slight negative signature and intermediate zone fluids indicating a strong influence from organic-rich or metamorphic sulfur reservoirs. Carbon and oxygen isotopic compositions (δ13C and δ18O) of calcite revealed a progression from marine carbonate signatures in marble samples (from +1.89 to +2.23‰VPDB; from +21.61 to +21.73‰VSMOW) to depleted values in prograde (from −6.0 to +0.09‰VPDB; from +6.22 to +18.14‰VSMOW) and retrograde skarns (from −3.8 to −2.25‰VPDB; from +0.94 to +3.62‰VSMOW), reflecting interactions with high-temperature magmatic fluids and meteoric water mixing. The fluid inclusions in prograde minerals generated under the conditions of fluid boiling exhibited high temperatures, reaching up to 412 °C, and salinities up to 26 wt.% NaCl equivalent. Conversely, the fluid inclusions in retrograde minerals, which were generated due to fluid mixing, exhibited lower temperatures (with an average of 318 °C) and salinities with an average of 4.9 wt.% NaCl equivalent. This indicated that the cooler and more diluted fluids mix with meteoric waters and interact with organic materials in the host rocks. This suggests a multifaceted origin involving various sources and processes. Therefore, this study concluded that the skarn mineralization in the Yolindi area resulted from complex interactions between magmatic, metamorphic, and meteoric fluids, reflecting a dynamic ore-forming environment with implications for the regional metallogeny of Cu-Fe skarn deposits.

Algama Gold Ore Cluster (Aldan–Stanovoi Shield): Mineralogy, Formation Conditions, Sources of Ore Matter, and Age of Mineralization

Abstract —The paper presents results of research into the conditions of formation of ores in the poorly studied Algama ore cluster (Bodorono deposit and Dyvok ore occurrence) located at the junction of the Aldan Shield and the Stanovoi area. We have established that Bi and Se minerals (bismuthinite, lillianite, native bismuth, tellurobismuthite, tetradymite, hedleyite, pilsenite, and laitakarite) are present in the ores of the Bodorono deposit. Two successive productive stages of mineral formation have been distinguished: Au–polymetallic and Au–Bi–Te. The corresponding minerals are products of the evolution of a hydrothermal system, during which a gradual decrease in fluid temperature (from 300 to 145 °C) and salinity (from 5 to 1.9 wt.% NaCl equiv.) took place. The fineness of native gold gradually increases from early (~840‰) to late (~940‰) stages and changes in passing from simple sulfides to sulfosalts. The evolution of the ore system is accompanied by a change in the composition of the vapor phase of fluid inclusions from CH4–CO2 to CO2 with an impurity of N2 and CH4. The results of 40Ar/39Ar dating of pre-ore metasomatites point to ore-forming processes at the Bodorono deposit ca. 150 ± 1.8 Ma. Analysis of the isotopic composition of lead in galena shows the leading role of the ancient crustal source of ore matter. The calculated isotopic composition of oxygen (δ18OH2O) in ore-bearing quartz varies from 1.0 to 7.3‰, which corresponds to an aqueous fluid of a mixed source. The Dyvok ore occurrence differs from the Bodorono deposit in the mineral composition of ores and the physicochemical parameters of ore formation. Four mineral stages have been established within the ore occurrence: gold–arsenopyrite–pyrite–quartz, pyrite–chalcopyrite–sphalerite, quartz–boulangerite, and telluride. The telluride stage is represented by hessite, altaite, volynskite, merenskyite, melonite, and rucklidgeite. Gold-bearing mineralization formed from a fluid of medium salinity (0.9–9.2 wt.% NaCl equiv.) with a predominance of CO2 and an impurity of CH4 in the vapor phase at moderate temperatures (310–360 °C). The calculated values of δ34S and δ18O varied from 2.2 to 3.0‰ and from 0.6 to 12.0‰, respectively. The 40Ar/39Ar age of gold mineralization is 124.0 ± 1.5 Ma, which corresponds to the stage of tectonomagmatic activity in the Aldan Shield.

Evolution of Ore-Forming Fluids at Azegour Mo-Cu-W Skarn Deposit, Western High Atlas, Morocco: Evidence from Mineral Chemistry and Fluid Inclusions

The Azegour Mo-Cu-W skarn deposit, located on the northern side of the Western High Atlas, occurs in lower Cambrian volcanic and sedimentary rocks. The mineralizations are linked to the hydrothermal alterations that affected carbonated layers of the lower Cambrian age during the intrusion of the calc-alkaline hyperaluminous Azegour granite. Four stages of the skarn and ore mineral deposition have been identified as follows. Firstly, (i) the early prograde stage and (ii) the late prograde stage. These prograde stages are characterized by anhydrous minerals (wollastonite, garnets, and pyroxenes) associated with scheelite mineralization. Based on mineral chemistry studies, the early prograde stage is dominated by andradite (Ad72.81–97.07) and diopside (Di61.80–50.08) indicating an oxidized skarn; on the other hand, the late prograde stage is characterized by a high portion of grossular (Gr66.88–93.72) and hedenbergite (Hd50.49–86.73) with a small ratio of almandine (Alm2.84–34.99), indicating “strongly reduced” or “moderately reduced” conditions with low f(O2). The next two stages are (iii) the early retrograde stage and (iv) the late retrograde stage, which contain hydrous minerals (vesuvianite, epidote, chlorite, muscovite, and amphibole) associated with sulfide. Fluid inclusions from pyroxene and quartz (prograde skarn stage) display high homogenization temperatures and high to low salinities (468.3 to >600 °C; 2.1 to >73.9 wt% NaCl equiv.). The boiling process formed major scheelite mineralization during prograde skarn development from dominated hydrothermal magmatic fluid solutions. By contrast, fluid inclusions associated with calcite–quartz–sulfide (retrograde skarn stage) record lower homogenization temperatures and low salinities (160 to 358 °C; 2.0 to 11.9 wt% NaCl equiv.). The distribution of the major inclusions types from the two paragenetic stages are along the trend line of fluids mixing in the salinity–homogenization temperature (magmatic water), illustrating the genesis of ore-forming fluid by mixing with fluids of low temperatures and salinities (metamorphic and meteoric waters).

A transition from porphyry Mo to vein-style Zn-Pb mineralization: Insights from hydrothermal fluid evolution of the Chalukou deposit, NE China

To reveal the hydrothermal evolution from porphyry Mo to vein-style Zn-Pb mineralization, the Chalukou deposit in NE China with these two typical mineralization overprinted is selected for detailed research. From early to late hydrothermal veins, the quartz cathodoluminescence intensities change from bright to dark and the textures also evolve. The Ti concentrations of quartz in these veins change from high to moderate and then to low values. The fluid inclusion petrography, microthermometry and stable isotope analyses indicate intermediate-density magma-derived fluids (δ18Owater = +4.7 to + 6.2‰, δD = −132 to −136‰) exsolved at high temperatures (560° to 600 °C) with low to moderate salinity (2.4 to 8.0 wt% NaCl equiv) containing minor CO2 (<5.7 mol %). Early minor molybdenite occurred under lithostatic conditions at high temperatures (540° to 580 °C) during fluids pH change and early magnetite precipitation. Later main molybdenite precipitation at moderate temperatures (350° to 430 °C), result from fluid cooling and involving of meteoric water under the transition from lithostatic to hydrostatic conditions. The precipitation of pyrite in transitional veins at moderate temperatures (330° to 420 °C), and the late sphalerite-galena from a lower-temperature fluid (180° to 300 °C) is consistent with the cooling of magmatic fluid, and gradually dilution with meteoric water under hydrostatic conditions. It is deduced the transition from porphyry Mo to vein-style Zn-Pb mineralization is likely driven by progressive decrease in temperature of the magmatic fluids and the increasing influx of meteoric water.

Tracing metal source of copper-rich tungsten mineralization: Evidence from individual fluid inclusion analysis of the Huangsha Cu-rich W deposit in South China

The Huangsha Cu-rich W deposit, located in the northeast part of the Nanling region, is a typical large-size wolframite-quartz vein-type W deposit with considerable reserves of copper. Wolframite and chalcopyrite usually distribute in the same quartz veins, while field and petrographic observation show that wolframite commonly precipitates earlier than coexisting quartz and sulfides. Veined quartz can be divided into three successive generations (Q1, Q2, and Q3) based on SEM-CL imaging, and only Q2 is strictly coeval with chalcopyrite and other sulfides. Primary two-phase aqueous (type Lw) fluid inclusions are identified from wolframite with homogenization temperatures of 292 to 327 ℃ and salinities of 6.9 to 9.9 wt% NaCl equiv. Pseudosecondary two-phase aqueous (type Lq) and vapor-rich (type Vq) fluid inclusions are recognized from Q2, supporting the occurrence of fluid immiscibility. Homogenization temperatures of type Lq inclusions in Q2 range from 200 to 258 ℃ with salinities of 4.3 to 7.7 wt% NaCl equiv. LA-ICP-MS analysis shows that all inclusions contain Na and K as the major cations. For all the detected elements, type Lw inclusions in wolframite have higher concentration ratios X/Na than type Lq inclusions to varying degrees. The ore-forming fluid in both W and Cu mineralization stages share the same characteristics of high B concentrations, consistent Rb/Cs ratios and evolving nature of ore metals, indicating that W and Cu were sourced from the same magmatic fluid but precipitated in different mineralization stages. The variation of fluid Sr concentration likely indicates fluid-rock interaction during precipitation of wolframite, whereas the deposition of chalcopyrite is possibly influenced by fluid cooling and immiscibility. Compared with typical porphyry Cu systems and W/Sn mineralized systems worldwide, the ore-forming fluid in the W mineralization stage at Huangsha shows considerably higher mineralization potential of Cu, which is consistent with the geological fact. The Cu contents in initial W ore-forming fluids may serve as an indicator in identifying Cu-rich W deposits.

Hydrothermal lead-zinc-copper mineralizations in sedimentary rocks of Northern Apennines (Italy)

Lead and zinc hydrothermal mineralizations associated with late Oligocene-early Miocene sedimentary rocks (sandstones and marls) were found and investigated for the first time in the Northern Apennines (Northern Italy, province of Reggio Emilia). The mineralizations are located in a structurally complex area involved in the tectonic events forming the Northern Apennines chain. They are stratabound mineralizations mainly in the form of sub-vertical veins, suggesting a strong structural control. The ore minerals are sphalerite and galena (rare chalcopyrite), the gangue minerals are carbonates, barite and quartz, in different proportions in the three investigated sites (Busana, Casalino, Casenove). On the basis of microthermometric data on fluid inclusions in ore and gangue minerals, the ore-forming fluids belonged to an aqueous system containing Na-, Mg-, Ca-chlorides and/or carbonate and had a relatively high salinity, mainly in the range 11–17 wt% NaCl equivalent. The trapping temperatures were relatively high (142–231 °C range), suggesting basins characterized by anomalous geothermal gradients. The sphalerite composition reveals different FeS contents and different Zn/Cd ratios in the three sites. The δ34S values of the ore minerals vary from −7.98/−10.98 ‰ in Busana to 4.38/6.85 ‰ in the other two sites. The barite in Casalino has values of δ34S = 25.56 ‰ and δ18O = 13.81 ‰. The sphalerite composition and the isotopic data suggest complex interactions of the basin fluids involving crossed sediments, evaporite rocks, organic matter, as well as mixing between fluids and Jurassic marine waters. On the basis of their geological, petrographic-mineralogical and geochemical features, these mineralizations can be considered Alpine- or Irish-type MVT mineralizations.

Magma-related origin for Pb–Zn–Ag vein formation at the Aerhada deposit, Inner Mongolia, NE China: Constraints from fluid inclusion, C–H–O–S–Pb isotopic compositions, and geochronological studies

The Aerhada Pb–Zn–Ag deposit is on the western margin of the Great Xing’an Range in NE China. Prior studies on this deposit lack information regarding precise mineralization age and convincing genetic interpretation, which limits both the prospecting at Aerhada and the reconstruction of the regional metallogenic evolution. Based on a detailed field investigation and microscopic observation, in this study, our aim was to determine the origin and evolution of the hydrothermal system and the timing of magmatism and mineralization, as well as to develop a possible metallogenic model, by revealing information regarding the mineralization paragenetic relationship, fluid inclusions, H–O–C–S–Pb isotopes, and sphalerite Rb–Sr and zircon U–Pb ages. Three successive mineralization stages were recognized: stage I quartz-arsenopyrite-pyrite, stage II quartz-sphalerite-galena, and stage III fluorite-calcite-pyrite. Four types of fluid inclusions were also identified in host minerals: CH4-rich two-phase, halite-bearing, vapor-rich two-phase, and liquid-rich two-phase. Fluid inclusion and microthermometric results showed that the homogenization temperatures were 287–341 °C for stage I, 237–291 °C for stage II, and 162–230 °C for stage III, with respective salinities of 1.7–40.2 wt%, 6.7–10.9 wt%, and 4.2–8.8 wt% NaCl equivalent. The δ18Ofluid and δDfluid values of quartz in stage I (δ18Ofluid = 8.6–10.3 ‰, δDfluid = -126.6 to −124.3 ‰) indicated that initial magmatic water interacted with organic strata, while decreasing the values of quartz in stage II (δ18Ofluid = 3.9–6.8 ‰, δDfluid = -129.1 to −127.6 ‰) and calcite in stage III (δ18Ofluid = -3.5 to −1.0 ‰, δDfluid = -115.5 to −113.4 ‰), showing a trend of dilution and cooling by meteoric water. The negative δCfluid values (δCfluid = -15.9 to −12.6 ‰) of quartz fluid inclusions from stages I and II emphasize that organic carbon was added to the hydrothermal system through water–rock interactions. The δ34S values (δ34Ssulfides = 1.2–7.5 ‰) and lead isotope data of sulfides (206Pb/204Pb = 18.153–18.684, 207Pb/204Pb = 15.370–15.750, 208Pb/204Pb = 37.653–39.301), coupled with those of the hidden biotite granite and Devonian strata, indicate that the ore-forming material was primarily derived from magma and wall rocks. The sphalerite samples produced a Rb–Sr isochron age of 154.1 ± 3.5 Ma (2σ, MSWD = 0.82, n = 8), which was like the zircon U–Pb age of biotite granite (156.3 ± 1.4 Ma, 2σ, MSWD = 0.89, n = 14). Combining the alteration pattern, fluid inclusions, and isotopic and geochronological studies, it was concluded that Aerhada is a magma-related hydrothermal Pb–Zn deposit formed under the post-collision extension setting following the Mongol–Okhotsk Ocean closure during the Late Jurassic period. The proposed metallogenic model is expected to assist in the exploration and development of polymetallic mineralization in the Great Xing’an Range.

Ore-Forming Fluids of Orogenic Gold Deposit In Tamilouw-Haya, Seram Island, Indonesia

The Tamilouw-Haya orogenic gold deposit is located in the southern arm of Seram Island, Indonesia, occupying Tehoru Metamorphic Complex. Gold mineralization is predominantly in the form of veins, stockwork, and breccia, although minor dissemination is slightly appeared in the rock float samples. Ore-mineral assemblages are dominated by native gold, pyrite, chalcopyrite, sphalerite, tetrahedrite-tennantite (sulfosalt), galena, pyrrhotite, marcasite, realgar, kalininite, and arsenopyrite. Covellite, hematite, goethite, and malachite appear as supergene minerals. High-grade gold ores in this area are generally found in quartz-carbonate veins with the main alteration processes involving silicification, carbonatization, and sericitic. The P-T history of the mineralization was revealed by fluid inclusions, and this study implies the depth of ore deposit and its evolution during mineralization. The primary fluid inclusions from three different types of quartz/quartz-carbonate veins in Tamilouw-Haya crystallized at the homogenization temperature (Th) of 240 °C to 340 °C, with a fluid salinity from 3.87 to 0.70 wt. % NaCl equivalent, and melting temperature (Tm) of -0.4 to -2.3 oC. The ore-forming fluids consist mainly of two-phase (VCO2+LH2O) liquid-rich aqueous inclusions, characterized by low to rich CO2, low salinity, and moderate temperature. There are three vein types as the ore-bearing fluids with precious metals and anomalous high basemetal contents. Quartz type 1- veins (V1); concordant veins, formed at a temperature of 240-307 oC with an average salinity of 1.8 wt. % NaCl equivalent. Quartz type 2- veins (V2) tend to cut the rock foliation which are formed at temperature range from 293-336 oC with the average salinity that shows a value of 2.4 wt. % NaCl equivalent. Meanwhile, type 3 quartz-carbonate veins (V3) are formed at the temperature range of 240-340 oC and the average salinity of 2.72 wt. % NaCl equivalent. These quartz-carbonate veins cut the wall-rock foliation, which is identified as the late stage and associated with ore deposition in Tamilouw-Haya. The gold deposit in Tamilouw-Haya is formed at a depth of about 5.5-9 km of paleosurface, and the pressure between 1.7-2.4 Kbar in epizonal to mesozonal zones. Keywords: Tamilouw-Haya, orogenic gold, fluid inclusion, microthermometry, ore-forming fluids

Metallogenic model of the Eocene Santa María and Antares Zn-Pb(-Ag) skarn deposits, Velardeña Mining District, Durango, Mexico

The Santa María and Antares Zn-Pb(-Ag) skarn deposits in the Velardeña Mining District are located in central–NW Mexico. They lie 470 m apart along the contact between Oligocene felsic intrusions and Cretaceous limestones, and were developed during prograde, retrograde, post-ore (Santa María), and late stages. Firstly, the prograde stage was formed by fluids at ~ 600 °C and 15 wt% NaCl equiv., and consists of garnet + wollastonite ± clinopyroxene and biotite ± K-feldspar assemblages. Secondly, the retrograde/ore stage was formed by fluids at 300–500 °C with salinities of 20–30 wt% CaCl2 (Santa María) and > 40 wt% NaCl equiv. (Antares). It comprises assemblages of chlorite, amphibole, epidote, calcite, scapolite, quartz, sericite, adularia, fluorite, and muscovite associated with sphalerite, pyrite, galena, pyrrhotite, arsenopyrite, chalcopyrite, and Pb-Bi-Sb sulfosalts. Thirdly, the post-ore stage was formed by fluids at ~ 400 °C and 20–30 wt.% CaCl2 and comprises poorly mineralized calcite veins. Fourthly, the late stage was formed by fluids at < 300 °C and 20–30 wt.% CaCl2 (Santa María) and ~ 15 wt% NaCl equiv. (Antares), and crystallized tetrahedrite-group minerals and pyrite + marcasite. δ18Ofluid between ~ 14‰ and 23‰ at Santa María and between ~ 12‰ and 17‰ at Antares show a less-modified magmatic affinity for mineralizing fluids at Antares; δ13Cfluid between 0‰ and –6‰ register recycling of sedimentary C. Moreover, sulfides with δ34SVCDT between –3‰ and 2‰ reveal a magmatic source for S. Altogether, these data suggest that, at Santa María, magmatic-derived fluids actively interacted with the wall rocks, whereas at Antares the fluid-rock interaction was milder. In both deposits, metal deposition was triggered by the cooling and neutralization of ore-bearing fluids with carbonate rocks. Our 40Ar/39Ar dates for adularia of ca. 37.5 Ma place the deposits within the Eocene–early Miocene metallogenetic epoch of central–NW Mexico, during which other world-class skarn-epithermal systems were emplaced (e.g., Concepción del Oro and Mazapil-Peñasquito).

Myauchan Ore Field (Northeastern Asia), an Example of Weakly Eroded Ag–Pb–Zn Volcanoplutonic Mineralization

Abstract —The Myauchan ore field located in the Omsukchan zone of the Okhotsk–Chukotka Volcanic Belt is described. The Korennoe and Malyutka Ag–Pb–Zn ore occurrences forming this field are localized at the center of anticlinal fold of NW strike made up of Upper Triassic carbonate-terrigenous deposits intruded by stock-like bodies and dikes of Upper Cretaceous andesite, monzodiorite, granite-porphyry, and rhyolite-porphyry. Sulfide–carbonate–fluorite–quartz veins and vein–veinlet zones with arsenopyrite, pyrite, sphalerite, galena, chalcopyrite, and Ag-tetrahedrite are localized both in intrusions and in terrigenous strata. The field bears As–Sb–Ag–Pb–Au–Bi–Cu–Zn–W mineralization. Study of fluid inclusions and REE and ore element patterns show that the field ores formed from chloride solutions with the participation of surface waters in hydrothermal-magmatic system under epithermal conditions. The ores were deposited from solutions with TDS = 0.5–9.0 wt.% NaCl equiv. in the temperature range 106–287 ºC. The ores containing ca. 70 ppm Ag and up to 1.2% Pb formed through boiling-off of solutions enriched in iron salts. The ores with Ag &amp;lt; 7 ppm and Pb ≤ 25 ppm were generated from diluted hydrothermal solutions with predominant sodium salts and potassium admixture. Mineralization of the Myauchan ore field marks the upper level of the Ag–Pb–Zn ore system similar to the Gol’tsovoe deposit.

Multi-stage magmatic fluid recharge and fluid mixing developed the Gongdongchong intermediate-sulfidation type epithermal Pb-Zn deposit, North Huaiyang, China: Constraints from petrography, fluid inclusion and in situ geochemistry studies of sphalerite

The Gongdongchong (GDC) lead and zinc deposit is located in the North Huaiyang (NHY) metallogenic belt, northern part of the Dabie orogen. Its Pb-Zn orebodies are predominately in the breccia pipe hosted by the Early Paleozic Foziling Group. Three stages of mineralization could be divided according to replacement relationships and petrography, and the ore and gangue mineral assemblages at the main base metal stage were recognized as combination of Fe-poor sphalerite + galena + pyrite + chalcopyrite + tetrahedrite with quartz and calcite. Three successive generations of sphalerite were distinguished through detailed petrographic observation on crystal-scale, namely Spc (core), Spm (mantle), and Spr (rim). Fluid inclusion petrography result shows that two-phase liquid-rich fluid inclusions are the dominant type in sphalerite. Microthermometric results show the homogenization temperatures and salinities of Spc ranged from 233 °C to 268 °C and 6.6 to 10.4 wt% NaCl equiv. While fluid inclusions in the Spm display homogenization temperatures of 241 °C to 284 °C, with salinities of 8.7 to 11.3 wt% NaCl equiv. This increasing trend may imply a magmatic fluid recharging from core to mantle. However, fluid inclusions in the Spr have homogenization temperatures of 231–254 °C, with salinities of 6.3–9.1 wt% NaCl equiv. A trend of mixing with meteoric water is manifested by the decrease of temperatures with decreasing salinities from mantle to rim. It suggests the combination of the magmatic fluid recharging and mixing of meteoric water should be the key mechanism responsible for the sphalerite precipitation at the GDC deposit. Meanwhile, the GDC deposit shows a similar range of homogenization temperatures and salinities with typical intermediate-sulfidation epithermal deposits, and these homogenization temperatures also correspond well with the geological thermometer results acquired by trace element concentrations of sphalerite. In addition, the sphalerite geochemical results obtained from trace elements as Mn, Co, In and Ge illustrate that the GDC Pb-Zn deposit shares a good consistence with epithermal Pb-Zn deposit.Based on the evidences presented above, combined with the geological and geochemical features, the GDC deposit can be classified as an intermediate-sulfidation epithermal deposit. Intermediate-sulfidation epithermal deposits usually share spatial and genetic relationships with porphyry deposits. This may provide new implication for the mineral exploration of porphyry deposits at depth in the NHY metallogenic belt.

Origin of Ag-Pb-Zn mineralization at Huanaote, Inner Mongolia, NE China: Evidence from fluid inclusion, H-O-S-Pb and noble gas isotope studies

The newly-discovered Huanaote Ag-Pb-Zn deposit, containing 1173 tons Ag with a grade of 154 g/t, is situated in the western part of the Great Xing’an Range metallogenic belt. The source of metals and the fluid evolution for this large metallogenic system are still ambiguous. Mineralized Ag-Pb-Zn veins are primarily hosted in Late Carboniferous monzogranite and Devonian slate. Three paragenetic stages of mineralization were recognized at Huanaote, including (stage I) early pyrite + arsenopyrite + quartz ± K-feldspar; (stage II) the main ore stage sulfide (sphalerite, galena, chalcopyrite and pyrite) + sulfosalt (freibergite, bournonite, wittichenite and tetrahedrite) + quartz + sericite + chlorite ± epidote ± fluorite; and (stage III) late pyrite + quartz + calcite. The homogenization temperatures of fluid inclusion assemblage for stages I and II range from 254 to 337 ℃ and 143 to 270 ℃, respectively, while the fluid salinity varied from 2.3 to 14.2 and 0.9 to 11.8 wt% NaCl equiv. for stages I and II, respectively. The fluid δ18OH2O and δDH2O values range from −0.4 to +6.2‰ and −116.8 to −104.8‰, respectively, indicating that the source of the fluids was primarily derived from a magma with less contribution from meteoric waters. Sulfur isotope analyses of sulfides exhibit δ34S values from −4.3 to +8.0‰, consistent with those observed in other Ag-Pb-Zn deposits in this region, suggesting the sulfur was mainly magmatic origin with minor sedimentary sulfur addition. Similarly, the Pb isotope compositions of sulfides resemble those of local Mesozoic magmatism, implying a Mesozoic magmatic source for the metals. Additionally, the noble gas isotope compositions, specifically the 3He/4He ratios (ranging from 4.41 to 7.18 Ra, mean of 5.56 Ra) for fluid inclusions,strongly support a deep magmatic fluid responsible for the formation of Huanaote deposit. Fluid cooling, mixing with meteoric waters and dilution are suggested to be important processes for Ag-Pb-Zn deposition at Huanaote.

Geology, fluid inclusions, and isotope signatures reveal hydrothermal evolution and genesis of the Aqishan Pb-Zn deposit in Eastern Tianshan and implications for exploration of skarn mineralization

The Aqishan deposit (1.97 Mt at 1.05 % Pb + Zn) is located in the Aqishan-Yamansu arc, on the southwest section of the Eastern Tianshan, Northwest China. Pb-Zn mineralization is mainly hosted by garnet skarn and the volcaniclastic rocks of the Yamansu Formation. To decipher the evolution of ore fluids and source(s) of ore-forming components, and constrain the ore genesis, a combination of geological work, fluid inclusions, and C-O-S-Pb isotope systematics is presented. Detailed field and microscopic observations reveal that the skarn alteration and ore formation at Aqishan could be divided into four hydrothermal stages, consisting of prograde skarn (I), retrograde skarn (II), quartz–sulfides (III), and carbonate stage (IV). Sphalerite and galena are the dominant ore minerals generally occurring as disseminations and veins with locally laminated ores in stage III. Fluid inclusion data show that the fluids responsible for prograde skarn are high-temperature (342–518 °C) and high-salinity (7.3–44.2 wt% NaCl equiv.), and recorded fluid phase separation from an intermediate-salinity supercritical fluid, which was exsolved from crystallizing granitic magma. Microthermobarometry results limit the retrograde alteration within the temperature range of 313 to 388 °C and trapping pressures of 98 to 241 bars (1.0–2.5 km), with pressure dropping from lithostatic to hydrostatic regimes associated with a phase separation event. The boiling fluid inclusions in ore stage quartz show that the Pb-Zn mineralization formed at 205–357 °C, with a decrease in temperature facilitating the precipitation of ore-forming metals from hydrothermal system. Carbon and oxygen isotope compositions of calcite indicate a predominantly magmatic source for ore fluids at Aqishan with later meteoric water involved. Bulk and in situ sulfur values of sulfides range from −6.4 to −0.7 ‰, consistent with a dominantly magmatic origin. Sulfides together with the granite porphyry and tuff, show relatively homogeneous Pb isotope compositions, indicating that abundant ore-forming metals were sourced from a magmatic reservoir with contribution from country rocks. Fluid inclusion study and available calcite C-O isotopes suggest that significant decrease in temperature and fluid-rock interactions remarkably contributed to the metal deposition at Aqishan. The skarn alteration with typical alteration assemblages of garnet–diopside is proposed as an effective mineral exploration target of skarn(–like) ores in Eastern Tianshan.

Mineralization process of the Mazhala Au–Sb deposit, South Tibet: Constraints from fluid inclusions, H-O-S isotopes, and trace elements

The Mazhala deposit is a typical Au-Sb deposit in the northern Himalayan orogenic belt that has increasingly attracted worldwide attentions. However, debates remain regarding the source of ore–forming fluid and its evolutionary process. Herein, we investigate the genetic and compositional evolutionary characteristics of different types of pyrite grains in order to better constrain the ore–forming fluid source and ore–forming processes by means of Using in-situ trace and sulfur isotope data of pyrite and inclusion temperature and H-O isotope data of quartz. Based on the occurrence and morphological features of pyrite, four types of pyrite (Py0, Py1, Py2, and Py3) have been identified. The framboids of pyrite Py0 have high contents of Au, Ag, Cu, Pb, and Sb, with Co/Ni < l, and their δ34S values range from −34.0‰ to −19.3‰, indicating a sedimentary-diagenetic origin. Py1 pyrite exhibits stark core-rim structure. The contents of Sn, Ti, Be and W in Py1c are higher, with Co/Ni > 1. The δ34S of Py1c ranges from 0.30 to 3.9‰ (mean = 1.7‰), indicating a magmatic hydrothermal transformation origin. Py1r, Py2, and Py3 differ greatly in pyrite morphology and trace element contents, with Co/Ni < 1, indicating as hydrothermal sedimentary transformation origin. The δ34S values of Py1r, Py2, and Py3 vary from 1.4 to 6.50‰, interpreted as the presence of metamorphic sulfur sources. The δ34S values of Py1-Py2-Py3 firstly increases and then decreases, indicatinga fluid mixing process. The Mazhala ore–forming fluid is typical of low temperature (270–291 °C), low salinity (1.1–5.0 wt%NaCl equiv) and CO2-enrichment, with H-O isotopic compositions of quartz resembling magmatic and/or metamorphic water, which makes us to infer a mixture of magmatic and/or metamorphic water source for the Mazhala ore-forming fluid. The early pyrite grains were dissolved and reprecipitated under the action of fluid. In the process of multistage hydrothermal interaction, Au and other trace elements were released from the primary pyrite lattice into the fluid, forming the gold–bearing ore–forming fluid. Separation of fluid phase coupled with significant change in the pH value of fluid prompted the co-precipitation of Au and Sb to form the Mazhala Au-Sb deposit.

Petrogenesis of the Weiling beryl-bearing granitic pegmatite – A giant LCT-type pegmatite in the Northern Wuyi area, South China

The Weiling granitic pegmatite is a super-large (ca. 9.20 million tons) LCT-type pegmatite body in the Northern Wuyi area of South China, with the typical mineral assemblage quartz, plagioclase, K-feldspar and muscovite as well as tourmaline (schorl-dravite), garnet (almandine-spessartine) and beryl. This overall unzoned pegmatite with locally layered texture has economic amounts of the rare metal mineral beryl and ultrapure quartz, and porcelain clay in its uppermost weathering parts. The 40Ar/39Ar dating of pegmatitic muscovite yielded a precise age of 405.33 ± 3.38 Ma, indicating this beryl-bearing pegmatite body was formed in the Early Devonian rather than in the Jurassic-Cretaceous as previously thought. Boron and Nd isotope data demonstrate that the pegmatitic melts have solely crustal sources and are most likely derived from partial melting of the ambient metasedimentary rocks from the Zhoutan Formation. Geochemical characteristics of pegmatitic minerals muscovite, beryl, tourmaline, garnet and K-feldspar and the absence of coeval fertile granites around this pegmatite suggest that the Weiling pegmatite most likely evolved from anatectic melts that did not experience significant fractionation. The pegmatitic melts were generated by low degrees of muscovite dehydration partial melting of local metasedimentary rocks rich in fluxing elements and rare metals. These melts experienced limited differentiation during ascent in the crust. The beryl mineralization formed in the medium-temperature (222–357 ℃), low-salinity (3.3–10.9 wt% NaCl equiv.) and high-density (0.62–0.86 g/cm3) H2O-NaCl-KCl-CO2-N2 system. These temperatures are much lower than typical granitic pegmatites, possibly reflecting late fluids derived from the pegmatitic magma and experienced post-crystallization alteration. The Weiling pegmatite represents a Be-bearing pegmatite that formed by partial melting of local metasedimentary rocks.

40Ar-39Ar dating, fluid inclusion, and isotopic constraints on the timing, fluid evolution, and deposition of the polymetallic Nuocang Pb–Zn deposit in the western Nyainqêntanglha belt

The Nyainqêntanglha polymetallic belt (NPB) is western China's foremost skarn Pb–Zn metallogenic belt. Significant progress has been made in determining these ore deposits' age and origin. However, the precipitation mechanisms and mineralization controls for these deposits remain unresolved. 40Ar/39Ar dating, fluid inclusion (FI), and H-O-S-Pb isotopic data are presented for the Nuocang deposit, a newly discovered polymetallic Pb-Zn skarn deposit in the western NPB, with the goal to trace age and, especially, the major fluid processes associated with hydrothermal evolution leading to the precipitation of ore. The muscovite yields an 40Ar-39Ar plateau age of 59.68 ± 0.60 Ma, which closely resembles typical skarn deposits within the NPB, indicating that it formed during the main collisional stage of the India–Eurasia continent. In the Nuocang base-metal skarn deposit, three ore-related stages can be discerned and subdivided: 1) the pre-ore stage, containing the prograde and early retrograde metasomatic skarn minerals, 2) the syn-ore stage, including the late retrograde metasomatic minerals and sulfides, and 3) the post-ore stage of quartz, calcite, and chlorite alteration. Correspondingly, three types of FI (L, V, and S type) have been identified. The ore-forming fluids evolved from moderate to high temperature between 340 and 440 °C primarily, but up to 571 °C, and moderate to high salinity (concentrated ∼8–18 wt% NaCl-equiv., but up to 48.1 wt% NaCl equiv.) in the pre-ore stage. During the syn-ore stage, the fluids were at low to moderate temperature (between 200 and 320 °C) and low salinity (∼2 to 12 wt% NaCl-equiv.) and developed in low temperature (∼120–200 °C) and low salinity (∼2–8 wt% NaCl equiv.) in the post-ore stage. The calculated δDH2O values of the transparent minerals were −180 to −106 ‰ during the pre-ore stage, −141 to −59 ‰ during the syn-ore stage, and −152 to −105 ‰ during the post-ore stage. The δ18OH2O values were −1.2 to 3.8 ‰ during the pre-ore stage, −4.7 to −2.3 ‰ during the syn-ore stage, and −10.9 to −5.0 ‰ during the post-ore stage, respectively.Based on these results, the magmatic fluids appeared to have gradually evolved into meteoric. Meteoric water is believed to play a significant role in metal deposition within magmatic-hydrothermal systems. Locally, boiling is also considered another key mechanism for ore precipitation. The S-Pb isotope values of the sulfide metals indicate that the metallogenic materials were predominantly derived from an upper crustal source mixing with minor amounts of mantle–derived components. This study suggests that the fluid mixing is related to geostatic pressure variations and infiltration of meteoric waters into the hydrothermal system and are key mechanisms triggering Pb-Zn ore deposition in the NPB.

Genesis of the Mengxing Pb-Zn deposit in Baoshan block, SW China: Constraints from geology, fluid inclusion and isotopes

The Mengxing Pb-Zn deposit is located in the central-southern Baoshan block, SW China, which contains over 1.02 Mt metals with the average Pb + Zn grade of 12.12 %. In this deposit, the orebodies are mainly stratabound and developed in the Silurian limestone of the Shangrenheqiao Formation. The mineral assemblage is mainly consisted of sulfides, quartz, calcite and barite. Based on petrographic observation, three mineralization stages have been recognized, including the pre-ore, syn-ore (including stage I and II) and post-ore stages. Fluid inclusion study shows that the ore-forming fluid in Mengxing deposit belongs to a NaCl-H2O-(CO2) system with medium–high temperature (187.3–320.1 °C) and medium–low salinity (2.1–17.9 wt% NaCl equiv.). H-O-S-Pb isotopic studies reveal that the ore-forming fluid dominantly originated from magmatic water, and reacted with organic matter preserved in sedimentary strata at stage I and mixed with metamorphic/meteoric water at stage II. The sulfur for mineralization was mainly contributed by magmatic sulfur. Marine sulfates preserved in Silurian sedimentary strata also contributed some ore-forming sulfur in stage II. The ore-forming metals in Mengxing deposit were jointly contributed by sedimentary strata and deeply concealed granitic magmatism. Based on these geological and geochemical characteristics, we suggest that the Mengxing Pb-Zn mineralization is Epithermal type and formed in multiple stages.

Genesis of the Fenghuangshan gold deposit, eastern Hebei, China: Insights from ore geology, fluid inclusion and H–O–S isotopes

The Jidong area is a vital gold province in North China, including plenty of metamorphic rock-hosted gold deposits. Whether ore-forming fluids are magmatic or metamorphic remains controversial. The genesis for gold mineralization in this gold province is ambiguous. The Fenghuangshan gold deposit lies on the eastern fragment of the Jidong gold province. In this paper, we present a detailed study on ore geology, fluid inclusions, and stable isotopes for the deposit to illustrate the characteristics of ore-forming fluids and ore genesis.The deposit occurs as gold-bearing quartz vein and disseminated- and veinlet-type mineralization. The main orebody named 7# is hosted in migmatitic granite, controlled by NE trending secondary fracture system. Four hydrothermal mineralization stages were identified, including: (Ⅰ) white quartz, (II) pyrite-quartz, (III) quartz-polymetallic sulfide, and (IV) calcite-chlorite-quartz. The Stage II and III belong to main gold mineralization stage. Fluid inclusions from different stages show that a lowering trend of fluid inclusion homogenization temperature was observed. They ranged from 222 °C to 407 °C (early-stage), 144 °C to 375 °C (main-stage), and 86 °C to 174 °C (late-stage), respectively. The salinities of the ore-forming fluids were typically low, ranging from 0.83 to 15.47 wt% NaCl equivalent. On the basis of Laser Raman analysis and fluid inclusion microthermometry, the ore-forming fluids belonged to a low- to moderate-temperature, low-salinity H2O-NaCl-CO2 system. Fluid immiscibility gave rise to rapid gold deposition. The early-stage δD and δ18OH2O values from quartzs ranged from –96.4‰ to –92.5‰ and from 1.74‰ to 2.44‰, whereas main-stage fluids had δ18OH2O values of –4.10‰ to –3.50‰ and δD values of –91.5‰ to –89.5‰. The early- and main-stage sulfide δ34S values varied from –2.0‰ to + 2.2‰, with average values of + 0.4‰. H-O-S-isotope data indicated that the primary ore-forming fluids were magmatic water mixing meteoric water during mineralization, and ore-forming materials were derived from a homogeneous magmatic source. Ore geology, fluid inclusions, and stable isotopes illustrate that the Fenghuangshan gold deposit is a low- to moderate-temperature magmatic-hydrothermal gold deposit. Future deep-seated and surrounding gold exploration should center on this area.