Jusa and Barsuchi Log Volcanogenic Massive Sulfide Deposits from the Southern Urals of Russia: Tectonic Setting, Structure and Mode of Formation

The Jusa and Barsuchi Log volcanogenic massive sulfide (VMS) deposits formed along a paleo island arc in the east Magnitogrosk zone of the Southern Urals between ca 398 and 390 Ma. By analogy with the VMS deposits of the west Magnitogrosk zone, they are considered to be Baimak type deposits, which are Zn‐Cu‐Ba deposits containing Au, Ag and minor Pb. Detailed mapping and textural analysis of the two deposits shows that they formed as submarine hydrothermal mounds which were subsequently destroyed on the sea floor under the influence of ocean bottom currents and slumping. Both deposits display a ratio of the length to the maximum width of the deposit >15 and are characterized by ribbon‐like layers composed mainly of bedded ore and consisting principally of altered fine clastic ore facies. The Jusa deposit appears to have formed in two stages: deposition of colloform pyrite followed by deposition of copper–zinc–lead sulfides characterized by the close association of pyrite, chalcopyrite, sphalerite, galena, tennantite, arsenopyrite, marcasite, pyrrhotite, bornite, native gold and electrum and high concentrations of gold and silver. The low metamorphic grade of the east Magnitogorsk zone accounts for the exceptional degree of preservation of these deposits.     

Chemical Composition of Ores from the Takara Volcanogenic Massive Sulfide Deposit, Central Japan

Abstract. The Takara volcanogenic massive sulfide (VMS) deposit occurs in Miocene formation of the Misaka Mountain, the South Fossa Magna region, central Japan. The tectonic setting of the Misaka Mountain is reconstructed to be a part of the paleo Izu-Ogasawara arc which collided with the Honshu arc and to form accreted body in the present position. The Takara deposit, therefore, is considered to have formed in the paleo Izu-Ogasawara arc.
The ores from the Takara deposit are classified into pyrite-type ore, chalcopyrite-type ore, and sphalerite-type ore on the basis of chemical composition and their mineral assemblages. Some pyrite-type ores are characterized by their high Au content. The Au content is hardly recognized in the chalcopyrite-type and sphalerite-type ores.
The ores from the Takara deposit have intermediate bulk chemical composition between those from the Besshi-type deposits and the Kuroko-type deposits that are two representative VMS deposits. However, the bulk chemical composition is closer to that from the Kuroko-type deposits. And moreover, chemical composition of tetrahedrite-tennantite series minerals (tetrahedrite) is similar to that from the Kuroko-type deposits. The bulk chemical composition (Cu, Zn, Co, Pb, and As contents) of ores is affected by the chemical composition of volcanic rocks associated with VMS deposits.     

Metallogenic Province and Large Scale Mineralization of Volcanogenic Massive Sulfide Deposits in China

Volcanogenic massive sulfide (VMS) deposits are one of the most important base–metal deposit types in China, are major sources of Zn, Cu, Pb, Ag, and Au, and significant sources for Co, Sn, Se, Mn, Cd, In, Bi, Te, Ga, and Ge. They typically occur at or near the seafloor in submarine volcanic environments, and are classified according to base metal content, gold content, or host-rock lithology. The spatial distribution of the deposits is determined by the different geological settings, with VMS deposits concentrated in the Sanjiang, Qilian and Altai metallogenic provinces. VMS deposits in China range in age from Archaean to Mesozoic, and have three epochs of large scale mineralization of Proterozoic, Palaeozoic and Mesozoic. Only Hongtoushan Cu–Zn deposit has been recognized so far in an Archaean greenstone belt, at the north margin of the North China Platform. The Proterozoic era was one of the important metallogenic periods for the formation of VMS mineralization, mainly in the Early and Late Proterozoic periods. VMS-type Cu–Fe and Cu–Zn deposits related to submarine volcanic-sedimentary rocks, were formed in the Aulacogens and rifts in the interior and along both sides of the North China Platform, and the southern margin of the Yangtze Platform. More than half of the VMS deposits formed in the Palaeozoic, and three important VMS–metallogenic provinces have been recognized, they are Altai–Junggar (i.e. Ashele Cu–Pb–Zn deposit), Sanjiang (i.e. Laochang Zn–Pb–Cu deposit) and Qilian (i.e. Baiyinchang Cu–Zn deposit). The Triassic is a significant tectonic and metallogenic period for China. In the Sanjiang Palaeo–Tethys, the Late Triassic Yidun arc is the latest arc–basin system, in which the Gacun-style VMS Pb–Zn–Cu–Ag deposits developed in the intra-arc rift basins, with bimodal volcanic suites at the northern segment of the arc.     

Stratigraphic Correlation of the Malusok Volcanogenic Massive Sulfide Deposits, Southern Mindanao, Philippines

Abstract: Two adjacent volcanogenic massive sulfide (VMS) deposits, the Main Malusok and the Malusok Southeast, are delineated within Barangay Tabayo, Siocon, Zamboanga del Norte, Mindanao, Philippines. These deposits comprise massive to semi-massive sulfide lenses representing the down-dip equivalent of oxidized gossans. The massive sulfides have a primary mineral assemblage of pyrite-chalcopyrite-sphalerite with significant amounts of supergene copper in the form of chal-cocite. Owing to structural and metamorphic overprinting combined with intense alteration, primary textures are generally obliterated. Rock types are classified according to dominant mineral assemblages whereas the main lithologic units comprising the Malusok volcanic package are divided based on the position of each unit relative to the mineralized zone. The main lithologic units are designated as the hanging wall, the host, and the footwall sequences. In correlating the stratigraphy of the Main Malusok zone with that of the Malusok Southeast zone, a chlorite/epidote-rich interval located at the base of the hanging wall sequence serves as a distinct stratigraphic marker from which all lithologies are referred to. Comparisons between the stratigraphy of the two areas show that massive to semi-massive sulfide lenses are confined within a single stratigraphic interval representing the favorable horizon for the entire Malusok area. However, differences exist relative to style of mineralization and configuration of the altered interval between the Main Malusok and the Malusok Southeast VMS deposits. Based on characteristics exhibited by each individual deposit, it is inferred that the Main Malusok VMS deposit overlies a feeder zone whereas the Malusok Southeast sulfide lenses represent satellite deposits and transported blocks.     

Mineralogical and Genetical Aspects of the Doyashiki Kuroko Deposits, Hokuroku Basin, Japan

Abstract. A detail investigation of ore and gangue minerals was performed on the Doyashiki Kuroko deposits, Hokuroku basin, Japan for the first time. Main ore minerals are sphalerite, galena, pyrite, chalcopyrite, tetrahedrite-tennantite and digen-ite. Small amounts of enargite, wittichenite, electrum, covellite, bornite, marcasite and hematite are also observed. Quartz, barite and gypsum are common gangue minerals. Homogenization temperatures and salinities of fluid inclusions in quartz, sphalerite and barite range from 190 to 240C and 3.0 to 5.5 wt% NaCl equivalent, respectively. The FeS contents of sphalerite and Ag contents of electrum were 0.12 to 0.18 mol %, 39.0 to 39.6 atom %, respectively. The chemical composition of digenite as a primary mineral shows high sulfur contents.
These data indicate that ore fluid responsible for digenite and associated ore minerals was characterized by a range of high sulfur fugacity with a moderate formation temperature. This is concordant with the mineral assemblage of bornite-pyrite and chalcopyrite, which shows high sulfur fugacity conditions. It seems that the mineralization closely associated with acidic volcanism has occurred around 13 Ma of Middle Miocene on the seafloor at the depth of about 1500 m.     

Re-Os Dating of Sulfides from the Volcanogenic Massive Sulfide Deposit at Gacun, Southwestern China

Abstract. The Re-Os isotopic compositions of sulfide ores were analyzed for the Gacun, a volcanogenic massive sulfide deposit in southwestern China, to constrain the timing of mineralization. Sulfide ores from the deposit have a wide range of Re and Os concentrations, varying from 80.2 to 1543.2 ppb and from 0.307 to 8.83 ppb, respectively, and yielded a limited field of high ¹⁸⁷Re/¹⁸⁸Os and high ¹⁸⁷Os/188Os ratios, ranging from 1452 to 3309 and from 5.77 to 13.24, respectively. All sulfide samples yielded an isochron with an age of 217±28 Ma and an initial ¹⁸⁷Os/¹⁸⁸Os ratio of around 0.52±0.73. The Re-Os isochron age agrees with ages previously constrained by the other isotopic dating of the host rocks and fossil strata for the deposit. The rhythmic variation in ¹⁸⁷Os/¹⁸⁸Os and ¹⁸⁷Re/¹⁸⁸Os ratios within massive sulfide zone records a complicated process for ore-forming fluids episodically vented into the brine pool on the Mesozoic seafloor.     

Exploration Indices and Mineral Potential Map of the Kuroko Deposits in Northeast Japan

Abstract. Recent discoveries of seafloor hydrothermal mineralization in submarine volcanic centers of felsic magma in western Pacific island arcs are regarded as modern analogues of Kuroko type deposits. Studies of these deposits and their surrounding geology raised question whether the exploration activity for the Kuroko deposits on land which peaked in the 1960's was adequate or not. However, such an evaluation is not easy because the exploration data are about to be lost as a result of the closure of all the Kuroko mines in the area since 1994.
The Metal Mining Agency of Japan (MMAJ), therefore, decided to compile existing data on about 180 Kuroko deposits and related mineral occurrences in northeast Japan as a new Kuroko database.
This study extends a concept called "exploration indices" which was developed based on a case study of the thoroughly surveyed Hokuroku district to draw a potential map of the Kuroko occurrences for the entire northeast Japan quantitatively with a Geographical Information System (GIS). Effective exploration indices include: 1) distribution of dacitic-rhy-olitic submarine volcanic rocks of the Nishikurosawa and Onnagawa stages, 2) distribution of intrusive rocks of pre- and post-Kuroko horizon, 3) low aeromagnetic anomaly caused by hydrothermal alteration of magnetite, 4) low gravity anomaly which suggests depressions in the basement rocks such as a tectonic basin and/or caldera, and 5) nearby existence of vein type deposits. It is concluded that about 33 % of known Kuroko deposits fall within the high potential zone (score=4 and 5) that occupies only 4 % of the entire northeast Japan arc. The Kuroko potential map is, therefore, useful for limiting the target area for Kuroko type deposits in an island arc setting.     

"Brown Ore" from the Fukasawa Kuroko Deposits, Northeast Japan: Its Characteristics and Formation Process

Abstract: Brown–colored sulfide ore (brown ore) occurs in the easternmost part of the Tsunokakezawa No. 1 orebody of the Fukasawa kuroko-type deposits, northern Honshu, Japan. As this type of ores also occur in the marginal or uppermost part of several other kuroko deposits in Japan, the formation of brown ore appears to be repeated in the process of kuroko formation. The brown ore is characterized by its higher Ag concentration (up to around 2000 g/t) than ordinary black ore (Zn–Pb ore) of volcanogenic massive sulfide deposits. The brown ore from the Fukasawa deposits can be divided into following three ore types based on its texture and mineral composition: pyritic brown ore, principal brown ore and “diseased” brown ore. Primary precipitation textures such as framboidal– and colloform-textures and compositional zoning within sulfide grains are significant in the brown ores. This seems to be due to lack of overprinting high temperature mineralization resulting in preservation of primary features. The Ag-Au mineralization is widely observed within the brown ores. Silver and gold are especially concentrated in the barite veinlets in the principal brown ore, which are supposed to be fillings of conduit of hydrothermal solution precipitated in the latest stage of hydrothermal activity. This mineralization seems to occur at waning stage of brown ore formation by ore solution at a lower temperature (around 250°C) than that of main part of brown ore (around 270°C). Relatively low fluid temperature and contribution of oxic ambient seawater may be responsible for the development of the Ag-Au mineralization in the brown ore. The occurrence of framboidal-rich pyritic brown ore having negative δ³⁴S values (less than –10%) and filamentous texture of sphalerite, seeming remnant of bacteria, indicate the presence of intensive microbial activity in the hydrothermal area for brown ore formation. Formation environment of each ore type of the brown ore is supposed to be as follows: Pyritic brown ore is likely to have formed on the sea-floor around redox boundary at temperature (around 240°C) lower than ordinary black ore. Principal brown ore seems to have been formed beneath the shell of the pyritic brown ore at temperature around 270°C. Footwall of the brown ore is disseminated tuff breccia corresponding to feeder zone of hydrothermal fluid. Overprinting chalcopyrite mineralization is not observed in the brown ore except in limited part of “diseased” ore, which occurs just above the disseminated tuff breccia. Based on the features distinct from the ordinary black ore, the brown ore can be regarded as a product in the marginal part of submarine hydrothermal system, where temperature and flow rate of hydrothermal solution was relatively low and microbial activity was intensive. The brown ore seems to well preserve its primary features after its deposition and might show the initial feature of some part of the ordinary stratiform black ore.     

Kuroko and Hydrocarbon Deposits from Northern Honshu,Japan: A Possible Common Hydrothermal/Magmatic Origin?

Abstract. Northern Honshu is the most important area for mineral and oil resources in Japan. Many kuroko deposits and oil and gas fields are distributed in two belts along the northeast Japan arc, the kuroko metal‐belt on the Pacific side and the oil‐belt on the Sea of Japan side. The kuroko deposits are located mainly in the Green Tuff strata which formed as a result of submarine vol‐canism during the late Miocene and Pliocene. Most of the source rocks of the oil and gas deposits formed at the same time as the kuroko deposits and some of them are located in reservoirs of hydrothermally‐altered volcanic rocks in the Green Tuff region. There is general agreement that the kuroko deposits formed as a result of submarine hydrothermal and magmatic activity whereas almost all petroleum geologists and geochemists consider that hydrocarbon deposits were generated independently of such activity. Since the discovery of hydrothermally‐generated petroleum in the Guaymas Basin, Gulf of California, however, it is clear that petroleum can be formed almost instantaneously in terrestrial and submarine hydrothermal areas. The paleo‐northeastern Sea of Japan is therefore considered to be a potential area for hydrothermal petroleum generation because thick organic‐rich sediments overlie an active submarine volcanic area. Several lines of geological and geochemical evidence suggest the possibility of hydrothermally‐enhanced maturation of organic matter and the contribution of magmatic activity to the formation of these deposits. Although most of the oil and gas in northern Honshu has been generated conventionally as a consequence of the high geothermal gradients there, it appears that some of the oil and gas fields may have formed as a result of extensive hydrothermal and magmatic activity during the late Miocene to Pliocene. Because of the much steeper angle of the faults in the vicinity of the Hokuroku basin than in the Akita basin, the magmatic contribution to the kuroko mineralization would have been far greater than to the oil and gas deposits of the Niigata and Akita basins. We therefore propose a strong relationship between metal and oil and gas generation in northern Honshu based on the structure and tectonics of the northern Honshu arc‐backarc system.     

Mineralogy and composition of Kuroko deposits from northeastern Honshu and their possible modern analogues from the Izu-Ogasawara (Bonin) Arc south of Japan: Implications for mode of formation

The Kuroko deposits of NE Honshu are a key type deposit for the study of volcanogenic massive sulfide deposits. However, these deposits have not been studied in detail since the early 1980's and knowledge of their mode of formation is now dated. In this study, we present the analysis of 12 samples of the Kuroko deposits, 12 samples of submarine hydrothermal minerals from the Sunrise deposit and 6 samples from Suiyo Seamount, both of which are located on the Izu-Ogasawara (Bonin) Arc, for 27 elements. For the Kuroko deposit, Cd>Sb>Ag>Pb>Hg>As>Zn>Cu are highly enriched, Au>Te>Bi>Ba>Mo are moderately enriched, In>Tl are somewhat enriched and Fe is not significantly enriched relative to the average continental crust. Within each of these deposits, a similar pattern of element associations is apparent: Zn–Pb with As, Sb, Cd, Ag, Hg, Tl and Au; Fe–Cu–Ba with As, Sb, Ag, Tl, Mo, Te and Au; Si–Ba with Ag and Au; CaSO₄. The enrichment of the chalcophilic elements in these deposits is consistent with hydrothermal leaching of these elements from the host rocks which are dominantly rhyolite–dacite in the case of the Kuroko deposits, rhyolite in the case of the Sunrise deposit and dacite–rhyolite in the case of the Suiyo Seamount deposit. However, this pattern of element enrichment is also similar to that observed in fumarolic gas condensates from andesitic volcanoes. This suggests that there may be a significant magmatic contribution to the composition of the hydrothermal fluids responsible for the formation of the Kuroko deposits, although it is not yet possible to quantify the relative contributions of these two sources of elements.The compositional data show that Sunrise and Suiyo Seamount deposits are much closer compositionally to the Kuroko deposits from NE Honshu than are the submarine hydrothermal deposits from the JADE site in the Okinawa Trough which contain, on average, significantly higher concentrations of Pb, Zn, Sb, As and Ag than each of these deposits. In spite of the greater similarity in tectonic setting of the Hokuroku Basin in which the Kuroko deposits formed to the Okinawa Trough (intracontinental rifted back-arc basin) compared to Myojin Knoll and Suiyo Seamount (active arc volcanoes), it appears that submarine hydrothermal deposits from Myojin Knoll and Suiyo Seamount are closer analogues of the Kuroko deposit than are those from the Okinawa Trough. The present data are consistent with the magmatic hydrothermal model for the formation of Kuroko-type deposits as formulated by Urabe and Marumo [Urabe, T., Marumo, K., 1991. A new model for Kuroko-type deposits of Japan. Episodes 14, 246–251].     

黑矿型矿床成矿物质来源：日本上向黑矿铼—锇和氦同位素证据

上向黑矿（Uwamuki Kuroko)是日本最典型的黑矿型矿床，它形成于日本岛弧中新世矢折岛弧裂谷环境，产于双峰式岩石组合的长英质火山岩系中。矿床由下部筒状硅矿带和上部块状黑矿带构成，后者显示典型的上黑（黑矿）下黄（黄矿）金属分带。为探索研究长期争议的成矿物质来源，系统测定了矿石和主岩的Os,He同位素组成。含矿流纹岩系的R／RA值介于0．93－1．14间，证实该岩浆可能主要来源于陆壳重熔。上向黑矿的上部块状黑矿矿石具较高的^187Os/^188Os值（2．246－7．608），反映矿石Os主体来源于壳源沉积物或矿区基底岩系；下部脉状－网脉状硅矿、块状黄矿和少量黑矿则具低^187Os/^188Os值（0．423－0．793），证实矿石Os具两源性，估计幔源物质贡献约57％－89％，壳源物质贡献约11％－43％。此外，在上部块状黑矿带内部，矿石 ^187Os/^188O显示清楚的垂向韵律性变化，揭示了成矿流体及成矿物质的周期性混合，据此，本文提出了一个新的两阶段成矿模式。     

Trace Fossils and Sulfur Isotopes in Mudstones around the Kuroko Deposits in the Hokuroku Basin, Northeast Japan: An Attempt to Delineate the Depositional Environment

Abstract. A comprehensive investigation was carried out on the distribution of both trace fossils and sulfur isotopes in mud-stones in the Hokuroku district, northeast Japan, in the hope of delineating the depositional environment of the mudstones in which the Kuroko deposits are embedded. The mudstones are generally massive in structure and usually contain large trace fossils, being indicative of an aerobic biofacies. On the other hand, some mudstones in and above the Kuroko ore horizon are partly laminated and usually contain smaller trace fossils, being assignable to an anaerobic or dysaerobic biofacies. The δ³⁴S values of sulfides in the mudstones above and below the ore horizon range from -40 to -12 %o, indicating mostly oxic depositional conditions in equilibrium with the inferred aerobic biofacies. In the mudstones in the ore horizon, the δ³⁴S values exhibit regionally discriminated variations: -44 to -12 %o in areas far (>1 km) from the known Kuroko deposits and -24 to +6 %o in areas closer to them. The latter high δ³⁴S group implies the temporal occurrence of local anoxic basins in the vicinity of the known Kuroko deposits. At the time of late Nishikurosawa Stage (i.e. the currently assumed Kuroko metallogenic epoch), an intense oceanic stagnation is suggested to have taken place to form the local anoxic basins responsible for the formation and preservation of Kuroko deposits. This oceanic environmental event is considered to be most likely due to increasing biological productivity primarily triggered and enhanced by upwelling of NADW in the paleo-Sea of Japan at that time.     

阿尔金山喀腊达坂一带火山成因块状硫化物型铅锌矿床地质特征及找矿前景

阿尔金山北缘喀腊达坂地区位于红柳沟-拉配泉弧后盆地(裂谷)内,中酸性火山岩及近东西向断裂构造十分发育,在喀腊达坂断裂分布的褐铁矿化、黄钾铁矾蚀变带内已发现多处地质特征相似的铅锌矿床;通过分析喀腊达坂铅锌矿床地质特征,认为该区铅锌矿床均属火山成因块状硫化物型;。分析了该区的控矿因素,总结了找矿标志,认为该区硫化物型铅锌矿具有优越的成矿条件和巨大的找矿前景。     

Petrochemical Investigation of the Antique Ophiolite (Philippines): Implications on Volcanogenic Massive Sulfide and Podiform Chromitite Deposits

Abstract: The Antique ophiolite, located in Panay island (west‐central Philippines), corresponds to several tectonic slices within the suture zone between the Philippine Mobile Belt (PMB) and the North Palawan Block (NPB). It includes dismembered fragments of a basaltic sequence, dominantly pillow‐lavas with minor sheet flows, rare exposures of sheeted dikes, isotropic gabbros, subordinate layered mafic and ultramafic rock sequences and serpentinites. Most of the ophiolite units commonly occur as clasts and blocks within the serpentinites, which intrude the whole ophiolitic body, as well as, the basal conglomerate of the overlying Middle Miocene sedimentary formation. The volcanic rock sequence is characterized by chemical compositions ranging from transitional (T)‐MORB, normal (N)‐MORB and to chemistry intermediate between those of MORB and island arc basalt (IAB). The residual upper mantle sequence is harzburgitic and generally more depleted than the upper mantle underlying modern mid‐oceanic ridges. Calculations using whole‐rock and mineral compositions show that they can represent the residue of a fertile mantle source, which have undergone degrees of partial melting ranging from 9‐22.5 %. Some of the mantle samples display chondrite‐nor‐malized REE and extended multi‐element patterns suggesting enrichments in LREE, Rb, Sr and Zr, which are comparable to those found in fore‐arc peridotites from the Izu‐Bonin‐Mariana (IBM) arc system. The Antique ultramafic rocks also record relatively oxidizing mantle conditions (Δlog f_O2 (FMQ)=0.9‐3.5). As a whole, the ophiolite probably represents an agglomeration of oceanic ridge and fore‐arc crust fragments, which were juxtaposed during the Miocene collision of the PMB and the NPB. The intrusion of the serpentinites might be either coeval or subsequent to the accretion of the oceanic crust onto the fore‐arc. Volcanogenic massive sulfide (VMS) deposits occur either in or near the contact between the pillow basalts and the overlying sediments or interbedded with the sediments. The morphology of the deposits, type of metals, ore texture and the nature of the host rocks suggest that the formation of the VMS bodies was similar to the accumulation of metals around and in the subsurface of hydrothermal vents observed in modern mid‐oceanic ridge and back‐arc basin rift settings. The podiform chromitites occur as pods and subordinate layers within totally serpentinized dunite in the residual upper mantle sequence. No large coherent chromitite deposit was found since the host dunitic rocks often occur as blocks within the serpentinites. It is difficult to evaluate the original geodynamic setting of the mineralized bodies since the chemistry of the host rocks were considerably modified by alteration during their tectonic emplacement. A preliminary conclusion for Antique is that the VMS is apparently associated with a primitive tholeiitic intermediate MORB‐IAB volcanic suite, the chemistry of which is close to the calculated composition of the liquid that coexisted with the podiform chromitites.     

Geochemical behavior of rare earth elements in hydrothermally altered rocks of the Kuroko mining area,Japan

In this study we analyzed the chemical composition of hydrothermally altered dacite and basalt from the Kuroko mining area, northeastern Honshu, Japan, by REE (rare earth element). Features of rare earth element analyses include: (1) altered footwall dacite exhibits a negative Eu anomaly compared with fresh dacite, suggesting preferential removal of Eu²⁺ from the altered dacite via hydrothermal solutions, (2) altered hangingwall dacite and basalt and dacite and basalt adjacent to ore deposits exhibit positive Eu anomalies compared with fresh dacite and basalt, suggesting addition of Eu²⁺ from hydrothermal solutions, (3) LREE ratio (∑LREE/∑REE) from altered dacite of chlorite–sericite zone and K-feldspar zone show a negative relationship with δ¹⁸O, and La/Sm ratios show a positive correlation with the K₂O index. These trends indicate the addition of light rare earth elements such as La to the altered dacite from hydrothermal solution and/or leaching of heavy rare earth elements such as Sm and Yb, (4) Principal component analysis (PCA) indicates that light rare earth elements enrichment is related to the formation of sericite zone near the Kuroko deposits but not to the formations of chlorite and K-feldspar zones, and (5) The correlations among REE features (LREE ratio, MREE ratio, HREE ratio, Eu/Eu?), δ¹⁸O and K₂O index are not found for montmorillonite zone, mixed layer clay mineral zone and mordenite zone. Therefore, it is inferred that sericite, chlorite and K-feldspar alterations are related to the Kuroko and vein-type mineralization, but montmorillonite and mordenite alterations are not related to the mineralizations, and probably they formed at the post-mineralization stage.     

Mechanisms for anhydrite and gypsum formation in the Kuroko massive sulfide–sulfate deposits,north Japan

The Sr, Ba, and rare earth elements (REEs) concentrations and Sr isotopic composition of anhydrite and gypsum have been determined for samples from the Matsumine, Shakanai, and Hanaoka Kuroko-type massive sulfide–sulfate deposits of northern Japan to evaluate the mechanisms of sekko (anhydrite and gypsum) ore formation. The Sr isotopic compositions of the samples fall in the range of 0.7077–0.7087, intermediate between that for middle Miocene (13–15 Ma) seawater (0.7088) (Peterman et al., Geochim Cosmochim Acta, 34:105–120, 1970) and that for country rocks (e.g., 0.7030–0.7050) (Shuto, Assn Geol Collab Japan Monograph 18:91–105, 1974). The Kuroko anhydrite samples exhibit two types of chondrite-normalized REE patterns: one with a decrease from light REEs (LREEs) to heavy REEs (HREEs) (type I), and another with a LREE-depleted pattern (type II). Based on the Sr content and isotopic ratio (assuming an Sr/Ca (mM/M) of 8.7 for seawater), anhydrite is considered to have formed by mixing of preheated seawater with a hydrothermal solution of Sr/Ca (mM/M) = ca. 0.59–1.36 under the condition in which the partition coefficient (Kd) ranges between ca. 0.5 and 0.7. This results in the formation of anhydrite with higher Sr content with an Sr isotopic value close to that of seawater under seawater-dominant conditions. Larger crystals of type II anhydrite are partly replaced by smaller ones, indicating that anhydrite dissolution and recrystallization occurred after or during the formation of sekko ore. Gypsum, which partially replaces anhydrite in the Kuroko deposits, also exhibits two distinct chondrite-normalized REE patterns. Because LREEs are likely to be more readily mobilized during dissolution and recrystallization, it is hypothesized that LREEs are leached from type I anhydrite, resulting in the formation of type II anhydrite with LREE-depleted profiles.     

Platinum group elements zoning and mineralogy of chromitites from the cumulate sequence of the Nurali massif (Southern Urals, Russia)

The Nurali lherzolite massif is one of the dismembered ophiolite bodies associated with the Main Uralian Fault (Southern Urals, Russia). It comprises a mainly lherzolitic mantle section, an ultramafic clinopyroxene-rich cumulate sequence (Transition Zone), and an amphibole gabbro unit.The cumulate section hosts small chromitite bodies at different stratigraphic heights within the sequence. Chromitite bodies from three different levels along a full section of the cumulate sequence and two from other localities were investigated. They differ in the host lithology, chromitite texture and composition, and PGE content and mineralogy. Chromitites at the lowest level, which are hosted by clinopyroxenite, form cm-scale flattened lenses. They have high Cr# and low Mg# chromites and are enriched in Pt and Pd relative to Os and Ir. At a higher, intermediate level, the chromitites are hosted by dunite. They form meter thick lenses, contain low Cr# and high Mg# chromites, have high PGE contents (up to 26,700 ppb), and are enriched in Os, Ir and Ru relative to Pt and Pd, reflecting a mineralogy dominated by laurite–erlichmanite and PGE–Fe alloys. At the highest level are chromitites hosted by olivine–enstatite rocks. These chromitites have high Cr# and relatively low Mg# chromites and very low PGE content, with laurite as the dominant PGE mineral.The platinum group minerals (PGMs) show extreme zoning, with compositions ranging from erlichmanite to almost pure laurite and from Os-rich to Ru-rich alloys, with variable and irregular zoning patterns.Two chromitite bodies up to 6 km from the main sequence can be correlated with the latter based on geochemistry and mineralogy, implying that the variations in chromitite geochemistry are due to processes that operated on the scale of the massif rather than those that operated on the scale of the outcrop.Pertsev et al. [Pertsev, A.N., Spadea, P., Savelieva, G.N., Gaggero, L., 1997. Nature of the transition zone in the Nurali ophiolite, Southern Urals. Tectonophysics 276, 163–180.] propose that the Transition Zone formed by solidification of a series of small magma bodies that partially overlapped in time and space. The magmas formed by successive partial melting of the underlying mantle. We suggest that this process determined the changing PGE geochemistry of the successive batches of magma. The PGE distribution fits a model of selected extraction from the mantle, where monosulphide solid solution–sulphide liquid equilibrium was attained until complete melting of the monosulphide solid solution. Later and localized variations in fS₂ resulted in the formation of different PGMs with complex zoning patterns.     

An experimental study on felsic rock–artificial seawater interaction: implications for hydrothermal alteration and sulfate formation in the Kuroko mining area of Japan

Experimental studies on the interactions between artificial seawater (ASW) and fresh rhyolite, perlite and weakly altered dacitic tuff containing a small amount of smectite suggest changing cation transfer during smectite-forming processes. Initially, dissolution of K from the rocks accompanies incorporation of Mg and Ca from ASW during both earlier (devitrification stage) and later smectite formation, whereas Ca incorporated with early smectite formation redissolves with progressive reaction. Barium mobility increases toward the later smectite-forming reactions. Therefore, the large amounts of barite, anhydrite and gypsum in Kuroko ore deposits are considered to have precipitated from hydrothermal solutions derived from the interaction with previously altered felsic rocks during late smectite formation, rather than by the reaction with fresh felsic rocks.Editorial handling: D. Lentz     

Pb-Pb age of sedimentary phosphorite reworking in Lower Riphean carbonate sediments,the Satka Formation of Southern Urals

The mineral composition and U-Pb and Rb-Sr systematics of phosphorites from the Satka Formation of Lower Riphean carbonates, the Burzyan Group of Southern Urals, are studied. Phosphorites occurring as small lenses between stromatolite layers are composed largely of fluorapatite with admixture of detrital quartz, feldspars, illite, and chlorite. Phosphorite samples have been subjected to stepwise dissolution in 1 N (fraction L-1) and 2 N (fraction L-2) HCl. As is established, the maximum apatite content is characteristic of fraction L-1, while fraction L-2 is enriched in products of dolomite and sulfide dissolution and in elements leached from siliciclastic components. The Sr content in the Satka apatites (280–560 ppm) is substantially lower as compared with that in unaltered marine apatite. The ⁸⁷Sr/⁸⁶Sr “initial ratio in the phosphorites studied (0.71705–0.72484) and host dolomites from the lower part of the Satka Formation is significantly higher than in the Early Riphean seawater that indicates a reset of the Rb-Sr original systems in sediments. The Pb-Pb age of 1340 ± 30 Ma (MSWD = 6.4) estimated based on 7 data points characterizing fractions L-1 and L-2 is younger than the formation time of overlying Burzyan sediments, being consistent, within the error range, with date of the Mashak rifting event recorded at the Early-Middle Riphean boundary. The comparative U-Pb characteristics of two soluble fractions (L-1 and L-2) and silicate residue of phosphorites show that epigenetic redistribution of Pb and U was characteristic of the phosphorite horizon only. The initial Pb isotope composition and μ (²³⁸U/²⁰⁴Pb) estimated according to model by Stacey and Kramers for the early diagenetic fluids in carbonate and phosphate sediments of the Satka Formation suggest that they were in isotopic equilibrium with erosion products of the Taratash crystalline complex.     

南秦岭东河地区金矿床特征及成因分析

南秦岭东河金矿位于南秦岭西段,属南秦岭成矿带西成金铅锌多金属成矿带的东延部分,为陕甘川金成矿三角地带.区内出露地层为中上志留统舟曲岩组、志留系—泥盆系大河店组,其中,中上志留统舟曲岩组上岩段(S2+3z3)是金矿化产出的主要层位;区内断裂构造十分发育,主要表现为平行分布的近东西的层间挤压破碎带,为区内主要的控矿构造;区内构造破碎带内及旁侧发育的石英脉与金矿化关系密切.工作区内共圈定金矿体8条,矿体均近东西走向,其中主要矿体Au-8长度390m,平均厚度2.54m,Au平均品位为2.41×10-6.东河地区金矿床主要受断裂构造的控制;其次岩性、岩浆岩对金矿的形成也起一定的作用.通过对本区成矿地质背景、矿床地质特征、控矿因素等方面的研究,认为研究区金矿床为沉积-叠加改造型中-低温热液金矿床.