阿尔金大平沟金矿床地质特征及成因初探

大平沟金矿处于阿尔金山北坡太古界托格拉格布拉克岩群的NWW向强应变构造带中，矿体主要为石英脉型和含金蚀变岩型，其形态，产状，规模严格受韧脆性剪切带控制，含矿围岩主要为韧脆性变形的闪长质碎粒岩，糜梭岩，与金矿化有关的围岩变主要有黄铁矿化，硅化，钾化等，且随蚀变强度的增强，金含量增高，属中低温变质，岩浆热液复合因型金矿床。     

Manganese and ferromanganese ores from different tectonic settings in the NW Himalayas,Pakistan

In Pakistan manganese and ferromanganese ores have been reported from the Hazara area of North West Frontier Province, Waziristan agencies in the Federally Administered Tribal Areas and the Lasbela-Khuzdar regions of Baluchistan. This study is focused on comparison of mineralogy and geochemistry of the continental ferromanganese ores of Hazara and the ophiolitic manganese ores of the Waziristan area of Pakistan. In the Hazara area, ferromanganese ores occur at Kakul, Galdanian and Chura Gali, near Abbottabad, within the Hazira Formation of the Kalachitta-Margala thrust belt of the NW Himalayas of the Indo-Pakistan Plate. The Cambrian Hazira Formation is composed of reddish-brown ferruginous siltstone, with variable amounts of clay, shale, ferromanganese ores, phosphorite and barite. In Waziristan, manganese ores occur at Shuidar, Mohammad Khel and Saidgi, within the Waziristan ophiolite complex, on the western margin of the Indo-Pakistan Plate in NW Pakistan. These banded and massive ores are hosted by metachert and overlie metavolcanics.The ferromanganese ores of the Hazara area contain variable amount of bixbyite, partridgeite, hollandite, pyrolusite and braunite. Bixbyite and partridgeite are the dominant Mn-bearing phases. Hematite dominates in Fe-rich ores. Gangue minerals are iron-rich clay, alumino-phosphate minerals, apatite, barite and glauconite are present in variable amounts, in both Fe-rich and Mn-rich varieties. The texture of the ore phases indicates greenschist facies metamorphism. The Waziristan ores are composed of braunite, with minor pyrolusite and hollandite. Hematite occurs as an additional minor phase in the Fe-rich ores of the Shuidar area. The only silicate phase in these ores is cryptocrystalline quartz.The chemical composition of the ferromanganese ores in Hazara suggests that the Mn–Fe was contributed by both hydrogenous and hydrothermal sources, while the manganese ores of Waziristan originated only from a hydrothermal source. It is suggested that the Fe–Mn ores of the Hazara area originated from a mixed hydrothermal–hydrogenetic source in shallow water in a ontinental shelf environment due to the transgression and regression of the sea, while the Mn ores of Waziristan were formed at sea-floor spreading centers within the Neo-Tethys Ocean, and were later obducted as part of the Waziristan ophiolite complex.     

Implication of Apatite and Anhydrite for Formation of an Iron‐Oxide‐Apatite (IOA) Rare Earth Element Prospect,Benjamin River,Canada

The Benjamin River apatite prospect in northern New Brunswick, Canada, is hosted by the Late Silurian Dickie Brook plutonic complex, which is made up of intrusive units represented by monzogranite, diorite and gabbro. The IOA ores, composed mainly of apatite, augite, and magnetite at Benjamin River form pegmatitic pods and lenses in the host igneous rocks, the largest of which is 100 m long and 10–20 m wide in the diorite and gabbro units. In this study, 28 IOA ore and rock samples were collected from the diorite and gabbro units. Mineralogical observations show that the apatite–augite–magnetite ores are variable in the amounts of apatite, augite, and magnetite and are associated with minor amounts of epidote‐group minerals (allanite, REE‐rich epidote and epidte) and trace amounts of albite, titanite, ilmenite, titanomagnetite, pyrite, chlorite, calcite, and quartz. Apatite and augite grains contain small anhydrite inclusions. This suggests that the magma that crystallized apatite and augite had high oxygen fugacity. In back scattered electron (BSE) images, apatite grains in the ores have two zones of different appearance: (i) primary REE‐rich zone; and (ii) porous REE‐poor zone. The porous REE‐poor zones mainly appear in rims and/or inside of the apatite grains, in addition to the presence of apatite grains which totally consist of a porous REE‐poor apatite. This porous REE‐poor apatite is characterized by low REE (<0.84 wt%), Si (<0.28 wt%), and Cl (<0.17 wt%) contents. Epidote‐group minerals mainly occur in grain boundary between the porous REE‐poor apatite and augite. These indicate that REE leached from primary REE‐rich apatite crystallized as allanite and REE‐rich epidote. Magnetite in the ores often occurs as veinlets that cut apatite grains or as anhedral grains that replace a part of augite. These textures suggest that magnetite crystallized in the late stage. Pyrite veins occur in the ores, including a large amount of quartz and calcite veins. Pyrite veins mainly occur with quartz veins in augite. These textures indicate pyrite veins are the latest phase. Apatite–augite–magnetite ore, gabbro–quartz diorite and feldspar dike collected from the Benjamin River prospect contain dirty pure albite (Ab₉₈Or₂–Ab₁₀₀) under the microscope. The feldspar dikes mainly consist of dirty pure albite. Occurrences of the dirty pure albite suggest remarkable albitization (sodic alteration) of original plagioclase (An_25.3–An₆₀ in Pilote et al., 2012) associating with intrusion of monzogranite into gabbro and diorite. SO₄^2? bearing magma crystallized primary REE‐rich apatite, augite and anhydrite reacted with Fe in the sodic fluids, which result in oxidation of Fe²⁺ and release of S^2? into the sodic fluids. REE, Ca and Fe from primary REE‐rich apatite, augite and plagioclase altered by the sodic fluids were released into the fluids. Then Fe³⁺ in the sodic fluids precipitated as Fe oxides and epidote‐group minerals in apatite–augite–magnetite ores. Finally, residual S^2? in sodic fluids crystallized as latest pyrite veins. In conclusion, mineralization in Benjamin River IOA prospect are divided into four stages: (1) oxidized magmatic stage that crystallized apatite, augite and anhydrite; (2) sodic metasomatic stage accompanying alteration of magmatic minerals; (3) oxidized fluid stage (magnetite–epidote group minerals mineralization); and (4) reduced fluid stage (pyrite mineralization).     

贵州天柱大河边铅锌矿床的发现及其意义

大河边重晶石矿床是一个世界级的超大型重晶石矿床。最近在该区重晶石矿床下部的震旦系陡山沱组碳酸盐岩(白云岩)和碎屑岩中,新发现一套规模较大、层位产出稳定的铅锌矿化。铅锌矿体和重晶石矿床具有"上部为重晶矿,下部为铅锌硫化物矿床"的矿化特征。铅锌矿段矿石矿物主要为闪锌矿、黄铁矿及方铅矿,含少量白铁矿、黄铜矿及磁黄铁矿;脉石矿物主要为石英和重晶石,少量白云石、热液磷灰石、炭沥青及钡冰长石。成矿流体特征类似于形成沉积喷流型铅锌矿床的流体特征。铅锌矿化中的硫源自局限海盆内早寒武世海水经硫酸盐还原作用提供。此种类似于喷流沉积型铅锌矿床在南华裂谷盆地一带矿化层位稳定、分布范围较广泛,体现早寒武世时在裂谷盆地内存在一次大规模的热液事件。天柱大河边铅锌矿床的发现具有重要的资源意义及区内该种矿床的勘查意义。     

Phosphorites of the Chiatura manganese deposit and specific features of their formation

The paper presents results of the detailed study of phosphorites from manganiferous beds of the Chiatura deposit. The relatively high-grade (P₂O₅ 20–28%) phosphorites are represented by various rocks ranging from the variety dominated by massive phosphates with a rare aleuritic admixture of quartz and feldspar grains to rocks mainly composed of terrigenous material with phosphates in the matrix. Phosphates make up the matrix of various organic remains: differently preserved diatom algae and microbial species. Some relatively large organic remains (in particular, sponge spicules) are typically composed of iron minerals (with manganese admixture) rather than phosphates. Manganese ores comprise phosphorite fragments composed of phosphatized cyanobacterial mat. Phosphorites of the Chiatura deposit were likely formed in a shallow-water zone away from the continental land.     

大平沟金矿床矿石特征与金的赋存状态

大平沟金矿床是受韧性剪切带控制的中温动力变质热液矿床，金矿石主要为蚀变糜棱岩型，夹少量钾长石石英脉型，矿石结构有变晶结构、交代－充填结晶结构两主要类型，矿石构造以块状构造、团块状构造、细脉状构造和浸染状构造为主。金呈独立金矿物（主要为自然金）出现，以包体金、裂隙金、连生金和粒间金等形式嵌布于黄铁矿、黄铜矿、石英、钾长石及方解石等主要载金矿和中，金矿物形态多样，粒度以中细粒为主。上述特点与我国东部地区产于太古变质岩（绿岩带）中的金矿床具有可对比性，也与矿床成因研究的认识相吻合。     

湖南沃溪钨-锑-金矿床的矿石组构学特征及其成因意义

通过对湖南沃溪矿床的宏观至微观尺度上的矿石组构学研究，揭示出矿床系同生热水沉积成因。层状矿体、细脉状矿化以及围岩蚀变之间的空间关系，指示了矿石与其所赋存的围岩同时形成。矿床形成后的变质—变形作用，主要使矿物发生重结晶、碎裂、位错以及小范围的再活化等。     

Geological and geochemical constraints on the genesis of the Xiangquan Tl-only deposit,eastern China

The Xiangquan Tl deposit, located in the northern part of the Middle–Lower Yangtze Valley metallogenic belt, eastern China, is the only known Tl-only deposit. It is hosted in micritic limestone, marl and mudstone of the Lower Ordovician Lunshan Formation. The orebodies are controlled by the Xiao–Xiaolongwang–Dalongwang anticline and two reverse faults, and are generally stratabound and lenticular. Tl is only ore metal contained in disseminated, massive, brecciated and banded ores. The ore is composed of Tl-bearing pyrite, and gangue minerals quartz, fluorite, barite and carbonate. Alteration minerals include fluorite, barite, fine grained quartz and carbonate. Tl occurs isomorphously replacing iron in the lattice of pyrite, and less commonly as tiny independent Tl-bearing minerals which may be lafossaite (TlAsS₂) or lorandite (TlCl) appearing as 0.1–1 μm-sized cubic crystals. Xiangquan is a submarine sedimentary deposit and demonstrates that Tl, as a normally dispersed element, can form not only part of poly-metallic deposits but also as independent Tl deposits.     

The Chailag-Khem fluorite-barium-strontium rare earth carbonatite occurrence, the Western Sayan Range, Russia

The geological and mineralogical data on the Chailag-Khem F-Ba-Sr-REE occurrence in the Western Sayan Range, Russia, are discussed. The chemical compositions of rocks, ores, and minerals (ICP-MS, Link) are reported. The occurrence is localized in a tectonic crush zone composed of Cambrian quartz-sericite slates intruded by quartz syenite porphyry. Ore mineralization occurs as veins, cement of tectonic breccia, and metasomatic disseminations in host rocks. Massive ore consists of calcite, strontianite, and quartz; impregnations of euhedral fluorite, ankerite, and bastnaesite crystals; and fine-grained barite aggregate. Accessory minerals include parisite, synchysite, barytocelestine, sulfides, rutile, and uraninite. Late metasomatic calcite and strontianite segregations and veinlets are abundant. In genetic, mineralogical, and geochemical features, the Chailag-Khem occurrence is similar to the Late Mesozoic carbonatite deposits of Central Tuva, of which the Karasug Fe-F-Ba-Sr-REE deposit is the largest and best known. All carbonatite deposits and occurrences are located within a longitudinal zone transverse to the major tectonic elements of the region.     

An unusual manganese silicate occurrence at the Hoskins mine,Grenfell district,New South Wales

Stratiform manganese silicate rocks overlie jasper and metabasah in the ?Middle Silurian Hoskins Formation at the Hoskins manganese mine near Grenfell, NSW. Two dominant mineral assemblages occur in the Mn silicate rocks: (1) a “reduced’ assemblage, probably gradational into underlying jasper, containing abundant rhodonite and/or tephroite, plus subordinate carbonates, quartz, hausmannite, spessartine and Ba minerals, and (2) a well‐laminated ‘oxidized’ assemblage rich in red Mn‐rich alkali pyroxene and amphibole, braunite, manganoan pectolite and minor Mn‐rich mica, alkali feldspars, carbonates, quartz and barite. Several Mn silicates implicitly contain trivalent Mn. The Mn silicate rocks are rich in Mn, Ba and Sr, and also contain anomalously high Co, Cu, As and W; oxidized assemblages are alkali‐rich. Bulk compositions and geological setting suggest a submarine volcanic exhalative origin for the precursors of the Mn silicate rocks and jasper. Metamorphism has occurred at upper greenschist facies with original high oxygen fugacity conditions in the exhalative sediments being largely reflected in the resulting assemblages. Although analogues of the reduced Mn silicate rocks are widespread in metamorphosed Mn deposits, equivalents of the oxidized assemblages appear to be particularly uncommon.     

Mineralogy of metamorphosed manganese deposits of the South Urals

A mineralogical investigation of metamorphosed manganese rocks was carried out at ore deposits related to the Devonian volcanic complexes of the Magnitogorsk paleovolcanic belt of the South Urals. The mineralogical appearance of these rocks is determined by three consecutively formed groups of mineral assemblages: (1) assemblages occupying the main volume of orebodies and formed during low-grade regional metamorphism (T = 200−250°C, P = 2–3 kbar); (2) assemblages of segregated and metasomatic veinlets that fill the systems of late tectonic fractures; and (3) assemblages of near-surface supergene minerals. Sixty-one minerals have been identified in orebodies and crosscutting hydrothermal veinlets. The major minerals are quartz, hematite, hausmannite, braunite, tephroite, andradite, epidote, rhodonite, caryopilite, calcite, and rhodochrosite. The mineral assemblages of metamorphosed manganese rocks (metamanganolites) are characterized. Chemical compositions of braunite, epidote-group minerals, piemontite, pyroxenes, rhodonite, pyroxmangite, and winchite are considered. The bibliography on geology and mineralogy of the South Ural manganese deposits is given.     

Mineralogy, chemistry and genesis of Nishikhal manganese ores of South Orissa, India

Manganese ores of Nishikhal occur as distinctly conformable bands in the khondalite suite of rocks belonging to the Precambrian Eastern Ghats complex of south Orissa, India. Manganese minerals recorded are cryptomelane, romanechite, pyrolusite, with minor amounts of jacobsite, hausmannite, braunite, lithiophorite, birnessite and pyrophanite. Goethite, graphite, hematite and magnetite are the other opaque minerals and quartz, orthoclase, garnet, kaolinite, apatite, collophane, fibrolite, zircon, biotite and muscovite are the gangue minerals associated with these ores. The mineral chemistry of some of the phases, as well as the modes of association of phosphorous in these ores have been established. The occurrence of well-defined bands of manganese ore; co-folding of manganese ore bands and associated metasedimentary country rocks; the min-eral assemblage of spessartite-sillimanite-braunite-jacobsite-hausmannite; the geochemical association of Mn-Ba-Co-Ni-Zn together with the Si versus Al and Na versus Mg plots of the manganese ores suggest that the Nishikhal deposit is a metamorphosed Precambrian lacustrine deposit. Continental weathering appears to be the source for manganese and iron. After deposition and probable diagenesis, the manganese-rich sediments were metamorphosed along with conformable psammitic and pelitic sediments under granulite facies conditions, and subsequently underwent supergene enrichment to produce the present deposit. Received: 14 March 1995 / Accepted: 11 April 1996     

Mineralogy of the Boroo Gold Deposit in the North Khentei Gold Belt,Central Northern Mongolia

Mineral assemblages and chemical compositions of ore minerals from the Boroo gold deposit in the North Khentei gold belt of Mongolia were studied to characterize the gold mineralization, and to clarify crystallization processes of the ore minerals. The gold deposit consists of low‐grade disseminated and stockwork ores in granite, metasedimentary rocks and diorite dikes. Moderate to high‐grade auriferous quartz vein ores are present in the above lithological units. The ore grades of the former range from about 1 to 3 g/t, and those of the latter from 5 to 10 g/t, or more than 10 g/t Au. The main sulfide minerals in the ores are pyrite and arsenopyrite, both of which are divisible into two different stages (pyrite‐I and pyrite‐II; arsenopyrite‐I and arsenopyrite‐II). Sphalerite, galena, chalcopyrite, and tetrahedrite are minor associated minerals, with trace amounts of bournonite, boulangerite, geerite, alloclasite, native gold, and electrum. The ore minerals in the both types of ores are variable in distribution, abundance and grain size. Four modes of gold occurrence are recognized: (i) “invisible” gold in pyrite and arsenopyrite in the disseminated and stockwork ores, and in auriferous quartz vein ores; (ii) microscopic native gold, 3 to 100 µm in diameter, that occurs as fine grains or as an interstitial phase in sulfides in the disseminated and stockwork ores, and in auriferous quartz vein ores; (iii) visible native gold, up to 1 cm in diameter, in the auriferous quartz vein ores; and (iv) electrum in the auriferous quartz vein ores. The gold mineralization of the disseminated and stockwork ores consists of four stages characterized by the mineral assemblages of: (i) pyrite‐I + arsenopyrite‐I; (ii) pyrite‐II + arsenopyrite‐II; (iii) sphalerite + galena + chalcopyrite + tetrahedrite + bournonite + boulangerite + alloclasite + native gold; and (iv) native gold. In the auriferous quartz vein ores, five mineralization stages are defined by the following mineral assemblages: (i) pyrite‐I; (ii) pyrite‐II + arsenopyrite; (iii) sphalerite + galena + chalcopyrite; (iv) Ag‐rich tetrahedrite‐tennantite + bournonite + geerite + native gold; and (v) electrum. The As–Au relations in pyrite‐II and arsenopyrite suggest that gold detected as invisible gold is mostly attributed to Au⁺¹ in those minerals. By applying the arsenopyrite geothermometer to arsenopyrite‐II in the disseminated and stockwork ores, crystallization temperature and logfs₂ are estimated to be 365 to 300 °C and –7.5 to –10.1, respectively.     

Accessory mineralogy of orangeite from Swartruggens, South Africa

Summary ?Orangeite occurring as a complex series of dikes at Swartruggens (South Africa), is host to a diversity of accessory minerals, the most common of which are apatite, barite and calcite. Less common, but important phases are perovskite, wadeite, an unidentified Ca–Ti–Fe-silicate, strontianite, unidentified Ca-REE phosphate, zircon, rutile, titaniferous magnetite, quartz and diverse sulphides. The accessory minerals show wide variations in their mode in different segments of the dike suite as a consequence of crystal sorting during flow differentiation. Compositional data are given for apatite, barite, calcite, perovskite, wadeite and the unidentified Ca–Ti–Fe-silicate. The accessory mineral suite is similar to that found in lamproites but is sufficiently distinct in composition and paragenesis to preclude inclusion with that clan. Differences include the common presence of groundmass calcite, barite and serpentine in the orangeite and the absence of typomorphic minerals (leucite, sanidine, richterite) of the lamproite clan. Received January 15, 2001; revised version accepted October 15, 2001     

Gold Mineralization of the Gatsuurt Deposit in the North Khentei Gold Belt,Central Northern Mongolia

Mineral assemblages, chemical compositions of ore minerals, wall rock alteration and fluid inclusions of the Gatsuurt gold deposit in the North Khentei gold belt of Mongolia were investigated to characterize the gold mineralization, and to clarify the genetic processes of the ore minerals. The gold mineralization of the deposit occurs in separate Central and Main zones, and is characterized by three ore types: (i) low‐grade disseminated and stockwork ores; (ii) moderate‐grade quartz vein ores; and (iii) high‐grade silicified ores, with average Au contents of approximately 1, 3 and 5 g t^?1 Au, respectively. The Au‐rich quartz vein and silicified ore mineralization is surrounded by, or is included within, the disseminated and stockwork Au‐mineralization region. The main ore minerals are pyrite (pyrite‐I and pyrite‐II) and arsenopyrite (arsenopyrite‐I and arsenopyrite‐II). Moderate amounts of galena, tetrahedrite‐tennantite, sphalerite and chalcopyrite, and minor jamesonite, bournonite, boulangerite, geocronite, scheelite, geerite, native gold and zircon are associated. Abundances and grain sizes of the ore minerals are variable in ores with different host rocks. Small grains of native gold occur as fillings or at grain boundaries of pyrite, arsenopyrite, sphalerite, galena and tetrahedrite in the disseminated and stockwork ores and silicified ores, whereas visible native gold of variable size occurs in the quartz vein ores. The ore mineralization is associated with sericitic and siliceous alteration. The disseminated and stockwork mineralization is composed of four distinct stages characterized by crystallization of (i) pyrite‐I + arsenopyrite‐I, (ii) pyrite‐II + arsenopyrite‐II, (iii) galena + tetrahedrite + sphalerite + chalcopyrite + jamesonite + bournonite + scheelite, and iv) boulangerite + native gold, respectively. In the quartz vein ores, four crystallization stages are also recognized: (i) pyrite‐I, (ii) pyrite‐II + arsenopyrite + galena + Ag‐rich tetrahedrite‐tennantite + sphalerite + chalcopyrite + bournonite, (iii) geocronite + geerite + native gold, and (iv) native gold. Two mineralization stages in the silicified ores are characterized by (i) pyrite + arsenopyrite + tetrahedrite + chalcopyrite, and (ii) galena + sphalerite + native gold. Quartz in the disseminated and stockwork ores of the Main zone contains CO₂‐rich, halite‐bearing aqueous fluid inclusions with homogenization temperatures ranging from 194 to 327°C, whereas quartz in the disseminated and stockwork ores of the Central zone contains CO₂‐rich and aqueous fluid inclusions with homogenization temperatures ranging from 254 to 355°C. The textures of the ores, the mineral assemblages present, the mineralization sequences and the fluid inclusion data are consistent with orogenic classification for the Gatsuurt deposit.     

Sorkhe‐Dizaj Iron Oxide–Apatite Ore Deposit in the Cenozoic Alborz‐Azarbaijan Magmatic Belt,NW Iran

The Sorkhe‐Dizaj iron oxide–apatite deposit in the Cenozoic Alborz‐Azarbaijan magmatic belt, NW Iran, is hosted mainly by a Late Eocene to Oligocene quartz‐monzonitic body, and subordinately in the Eocene volcanic and volcanoclastic sequences. The Sorkhe‐Dizaj intrusive body is an I‐type granitoid of the calc‐alkaline series. Mineralization is associated with actinolization, K‐feldspar, sericitic, propylitic, and tourmaline alteration types. The orebodies are massive, banded, stockwork, and breccia in shape and occur mainly along the fault zones within the quartz‐monzonitic intrusion, volcanic, and volcanoclastic rocks. Ore minerals dominantly comprise magnetite, apatite, and monazite, as well as minor amounts of chalcopyrite, bornite, and pyrite. Four major paragenetic stages are discriminated in the mineralization including early, oxide, sulfide, and late stage. The Sorkhe‐Dizaj deposit is similar in the aspects of host rock lithology, alteration, and mineralogy to the Kiruna‐type deposits associated with minor Cu sulfide minerals. Spatial and temporal association of the mineralization with the Late Eocene–Early Oligocene quartz‐monzonite intrusive body suggests that the ore fluid was probably related to magmatic activity.     

Mineralogy and genesis of the metamorphosed manganese silicate rocks (gondite) of Gowari Wadhona,Madhya Pradesh,India

Manganese silicate rocks, interbanded with manganese oxide orebodies, constitute an important stratigraphic horizon in the Mansar formation of the Sausar Group of Precambrian age in India. The manganese silicate rocks of Gowari Wadhona occupy the westernmost flank of the manganese belt of the Sausar Group. These rocks are constituted of spessartite, calcium-rich rhodonite, quartz, manganoan diopside, blanfordite (manganese bearing member of diopside-acmite series), brown manganese pyroxene (manganese bearing aegirine-augite), winchite (manganese bearing richterite-tremolite), juddite (manganese bearing amphibole with richterite, tremolite, magnesioriebeckite and glaucophane molecules), tirodite (manganese bearing amphibole with richterite, cummingtonite and glaucophane molecules), manganophyllite, alurgite, piedmontite, braunite, hollandite (and other lower oxides of manganese) with minor apatite, plagioclase, calcite, dolomite and microcline. A complete mineralogical account of the manganese-bearing phases has been given in the text. It has been shown that the juxtaposition of manganese silicate rocks with dolomitic marble, regional metamorphism to almandine-amphibolite facies and assimilation of pegmatite veins cutting across the manganese formation, were responsible for the development of these manganese silicate rocks and the unusual chemical composition of some of the constituent minerals. It has been concluded that the manganese silicate rocks of Gowari Wadhona were originally laid down as sediments comprising manganese oxides admixed with clay, silica etc. and were later regionally metamorphosed to almandine-amphibolite facies. All evidences indicate that rhodochrosite was not present in the original sediment and the bulk composition of the sediments was rich in manganese. These rocks agree entirely to the detailed nomenclature of the gondites enunciated by Fermor (1909) and amplified by Roy and Mitra (1964) and Roy (1966).     

Syngenetic origin for the sediment-hosted disseminated gold deposits in NW Sichuan,China: ore fabric evidence

Sediment-hosted disseminated gold deposits in NW Sichuan China have many features in common with the well-known Carlin-type deposits in the western United States. They are hosted by Middle–Upper Triassic turbidites composed of 1300–4300 m of rhythmically interbedded, slightly metamorphosed calcareous sandstone, siltstone, and slate. The ore bodies are typically layer- or lens-like in shape and generally extend parallel to the stratification of the host sedimentary rocks, with a strike length of tens to several hundreds of meters. The immediate host rocks consist mainly of calcareous slate and siltstone characterized by high contents of organic matter and diagenetic pyrite. The main primary ore minerals associated with gold mineralization include pyrite, arsenopyrite, realgar, and stibnite. Gangue minerals comprise mostly quartz, calcite and dolomite. Gold is extremely fine-grained, usually less than 1 μm, and cannot be seen with an electron microscope.Two types of ore mineralization have been recognized in the deposits. The stratiform ores are composed of rhythmical interbeds of sulfides (e.g., pyrite, arsenopyrite, realgar, stibnite) interpreted to be authigenic and detrital quartz, quartzite, sericite, and graphite of allogenic origin. They were folded and deformed concordantly with host rocks, and grade both vertically and laterally into normal country rocks. Another type of ore forms a network of numerous gold-bearing veins and veinlets of quartz–calcite–sulfides of millimeter-, centimeter-, decimeter-, and even meter-scale in width. The network ore randomly fills fissures, microfissures, and cleavages, but still is stratabound in character. Detailed studies on ore fabrics show abundant evidence for synsedimentary origins, although subsequent diagenesis, metamorphism, tectonic deformation, and epigenetic hydrothermal activity have significantly remolded the primary fabrics. Primary fabrics are shown either by rhythmical interbeds of different mineral components parallel to the bedding, or by the change of grain size of the same minerals such as pyrite, realgar, and stibnite. The layer inhomogeneity of the stratiform ore is clarified by parallel overprints of later schistosity planes, resulting in distinct grain orientation and elongation, aggregate polarization, and undulating extinction of ore minerals, especially of mechanically and chemically extremely mobile ones, such as realgar and stibnite.It is proposed that the stratiform ores in these Chinese deposits were most probably formed concurrently with their host Middle–Upper Triassic turbidites in submarine, hot spring environments, while the network mineralization was formed as a result of complicated processes such as diagenesis, weak metamorphism, tectonic deformation, and epigenetic hydrothermal activity, responsible for the remobilization or reworking of the pre-existing stratiform ores. Geochemical data also support this genetic model.