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1.
Most skarn deposits are closely related to granitoids that intruded into carbonate rocks. The Cihai (>100 Mt at 45% Fe) is a deposit with mineral assemblages and hydrothermal features similar to many other typical skarn deposits of the world. However, the iron orebodies of Cihai are mainly hosted within the diabase and not in contact with carbonate rocks. In addition, some magnetite grains exhibit unusual relatively high TiO2 content. These features are not consistent with the typical skarn iron deposit. Different hydrothermal and/or magmatic processes are being actively investigated for its origin. Because of a lack of systematic studies of geology, mineral compositions, fluid inclusions, and isotopes, the genetic type, ore genesis, and hydrothermal evolution of this deposit are still poorly understood and remain controversial.The skarn mineral assemblages are the alteration products of diabase. Three main paragenetic stages of skarn formation and ore deposition have been recognized based on petrographic observations, which show a prograde skarn stage (garnet-clinopyroxene-disseminated magnetite), a retrograde skarn stage (main iron ore stage, massive magnetite-amphibole-epidote ± ilvaite), and a quartz-sulfide stage (quartz-calcite-pyrite-pyrrhotite-cobaltite).Overall, the compositions of garnet, clinpyroxene, and amphibole are consistent with those of typical skarn Fe deposits worldwide. In the disseminated ores, some magnetite grains exhibit relatively high TiO2 content (>1 wt.%), which may be inherited from the diabase protoliths. Some distinct chemical zoning in magnetite grains were observed in this study, wherein cores are enriched in Ti, and magnetite rims show a pronounced depletion in Ti. The textural and compositional data of magnetite confirm that the Cihai Fe deposit is of hydrothermal origin, rather than associated with iron rich melts as previously suggested.Fluid inclusions study reveal that, the prograde skarn (garnet and pyroxene) formed from high temperature (520–600 °C), moderate- to high-salinity (8.1–23.1 wt.% NaCl equiv, and >46 wt.% NaCl equiv) fluids. Massive iron ore and retrograde skarn assemblages (amphibole-epidote ± ilvaite) formed under hydrostatic condition after the fracturing of early skarn. Fluids in this stage had lower temperature (220°–456 °C) and salinity (8.4–16.3 wt.% NaCl equiv). Fluid inclusions in quartz-sulfide stage quartz and calcite also record similar conditions, with temperature range from 128° to 367 °C and salinity range from 0.2 to 22.9 wt.% NaCl equiv. Oxygen and hydrogen isotopic data of garnet and quartz suggest that mixing and dilution of early magmatic fluids with external fluids (e.g., meteoric waters) caused a decrease in fluid temperature and salinity in the later stages of the skarn formation and massive iron precipitation. The δ18O values of magnetite from iron ores vary between 4.1 and 8.5‰, which are similar to values reported in other skarn Fe deposits. Such values are distinct from those of other iron ore deposits such as Kiruna-type and magmatic Fe-Ti-V deposits worldwide. Taken together, these geologic, geochemical, and isotopic data confirm that Cihai is a diabase-hosted skarn deposit related to the granitoids at depth. 相似文献
2.
The Prominent Hill deposit is a world-class iron oxide copper–gold (IOCG) deposit in South Australia, characterized by a high Cu/S ratio of the dominant Cu-(Fe) sulfides hosted by hematite breccias. It contains a total resource of 278 Mt of ore at 0.98% Cu and 0.75 g/t Au. Prominent Hill is one of several IOCG deposits and numerous prospects in the Olympic IOCG province that are temporally associated with the 1603–1575 Ma Gawler Range Volcanics, a large igneous province including co-magmatic granitoid intrusions of the Hiltaba Suite. Globally, IOCG deposits share many similar features in terms of their geological environment and mineral association. However, it is not yet clear whether sulfur and copper originate from the same source rocks and which hydrothermal redox processes created the characteristic iron oxide enrichment. Highly variable sulfur isotope compositions of sulfides and sulfates in IOCG deposits have previously been interpreted in terms of diverse sulfur sources that may include contributions from magmatic, sedimentary, seawater or evaporitic sulfur. In order to test these alternatives, we performed a detailed sulfur isotope study of Cu-(Fe) sulfides from Prominent Hill and IOCG prospects nearby. The Prominent Hill deposit shows a wide range in δ34SV-CDT between − 33.5‰ and 29.9‰ for Cu-(Fe) sulfides, and a narrower range of 4.3‰ to 15.8‰ for barite. Iron sulfides (pyrite, pyrrhotite) show a narrow range in sulfur isotope composition, whereas Cu-bearing sulfides show a much wider range, and more negative δ34SV-CDT values on average. We propose a two-stage sulfide mineralization model for the IOCG system in the Prominent Hill area, in which all hydrothermal sulfur is ultimately derived from a magmatic source that had a composition of 4.4 ± 2‰. The diversity in sulfur isotope composition can be produced by different fluid evolution pathways along reducing or oxidizing trajectories. A reduced sulfur evolution pathway is responsible for stage I mineralization, when intrusion-derived magmatic-hydrothermal fluids produced early pyrite and minor chalcopyrite at Prominent Hill, and iron ± copper sulfides in regional magnetite skarns and in some pervasively altered volcanic rocks of the Gawler Range Volcanics. Shallow-venting magmatic-hydrothermal fluids and subaerial volcanic gases that became completely oxidized by reaction with atmospheric oxygen produced sulfate and sulfuric acid with a sulfur isotope composition equal to their magmatic source. This highly oxidized ore fluid probably consisted dominantly of water from the hydrosphere, but contained magmatic solute components, notably sulfate, acidity and Cu. Sulfate reduction produced hydrothermal Cu sulfides with a wide range in sulfur isotope compositions from very negative to moderately positive values. Partial reaction of the Cu-rich stage II fluid with earlier stage I sulfides resulted in mixing of sulfur derived from sulfate reduction and from sulfides deposited during stage I. Modeling of the sulfur isotope fractionation processes in response to reducing and oxidizing pathways demonstrates that the entire spectrum of sulfur isotope data from stage I and stage II mineralization can be explained with a single, ultimately magmatic sulfur source. Such a magmatic sulfur source is also adequate to explain the complete spectrum of sulfur isotope data of other IOCG prospects and deposits in the Olympic province, including Olympic Dam. The results of our study challenge the conventional model that suggests the requirement of multiple and compositionally diverse sulfur sources in hematite-breccia hosted IOCG style mineralization. 相似文献
3.
The Aitik Cu–Au–Ag deposit in the Gällivare area in northern Sweden is Sweden's largest sulphide mine with an annual production of 35 Mt of ore, and the biggest open pit operation in northern Europe. It is proposed in the present study that the Aitik deposit represents a Palaeoproterozoic, strongly metamorphosed porphyry copper deposit that was affected ca. 100 Ma later by a regional IOCG-type hydrothermal event. Consequently, the Aitik deposit might represent a mixed ore system where an early copper mineralisation of porphyry type has been overprinted by later regional IOCG mineralisation.Several attempts have previously been made to genetically classify the Aitik Cu–Au–Ag deposit as a distinct ore type. New geochemical, petrographic, structural, and fluid inclusion results combined with published data have provided the opportunity to present new ideas on the genesis and evolution of the Aitik Cu–Au–Ag deposit. The emplacement of a ca. 1.9 Ga quartz monzodiorite that host the ore at Aitik was related to subduction processes and volcanic arc formation, and synchronous with quartz vein stockwork formation and porphyry copper mineralisation. Highly saline aqueous (38 wt.% NaCl) fluid inclusions in the stockwork veins suggest entrapment at 300 °C and a pressure of nearly 3 kbar, a high pressure for a typical porphyry copper ore, but consistent with conditions at associated deep root zones of intrusion-related magmatic–hydrothermal systems. The highly saline fluid formed disseminated and vein-type ore of mainly chalcopyrite and pyrite within comagmatic volcaniclastic rocks, and caused potassic alteration (biotite, microcline) of the host rocks. The early porphyry copper mineralising event was followed, and largely overprinted, by CO2 and aqueous medium- to high-salinity (16–57 wt.% salts) fluids related to a ca. 1.8 Ga tectonic and metamorphic event (peak conditions 500–600 °C and 4–5 kbar). Extensive deformation of rocks and redistribution of metals occurred. Magnetite enrichment locally found within late veins, and late amphibole–scapolite and K feldspar alterations within the deposit, are some of the features at Aitik implying that aqueous fluids responsible for IOCG-mineralisation (200–500 °C and ~ 1 kbar) and extensive Na–Ca alteration in the region during the 1.8 Ga tectonic event also affected the Aitik rocks, possibly leading to addition of copper ± gold. 相似文献
4.
The Ediacaran BISF at Hormuz Island is a newly identified glaciogenic iron-salt deposit in the Tethyan margin of Gondwana. The BISF was formed by synchronous riftogenic A-type submarine felsic volcanism and evaporate deposition. The mineralization occurs in a proximal felsic tuff cone and jaspilitic distal zones and contains 1 million tonne of hematite-rich ore with an average grade of 58% Fe. The ore structure shows cyclicity of macrobandings, mesobandings and microbandings of anhydrite, halite, hematite and chert, which marks a new record in BIFs geohistory. The alteration minerals in the proximal and distal zones are actinolite, ripidolite, epidote, sericite, tourmaline, clinochlore, anhydrite and clay minerals. The occurrence of metamorphosed polygenetic bullet-shape dropstones in BISF attests that there was probably a continuous process of ice melting, episodic submarine volcanism and exhalative hydrothermal banded iron salt formation during the Late Ediacaran time. The non-metamorphosed Neoproterozoic stratigraphy, the presence of genus Collenia, U-Pb dating (558 ± 7 Ma) and the marked negative δ13C excursion in cap carbonates are representative of Late Ediacaran glaciation, which has been identified worldwide. The REE+Y display light REE enrichment, unusually strong Tb-Tm anomaly, a weak positive Y anomaly, but no distinguished Eu and Ce anomalies, reflecting the glaciogenic nature of the BISF. The contents of Zr, Hf, Nb, Ta, Th, La, Ce and Y in BISF, dropstones, halite and cap carbonates are similar to those of the Neoproterozoic glaciogenic BIFs. Also, the Ni/Fe, P/Fe ratios and Fe/Ti – Al/Al + Fe + Mn + Ca + Na + K diagram suggest an exhalative hydrothermal Ediacaran-type BISF. The absence of brecciated magnetite in the ore association and the low contents of copper (9–493 ppm) and gold (<5–8 ppb) are not in favor of the IOCG – Kiruna-type iron oxide ores. The co-paragenesis of hematite with several alteration minerals, in particular actinolite, tourmaline and anhydrite, indicates that the exhalative hydrothermal fluids were generated by the interaction of seawater with the felsic rocks and sediments at about 200–500 °C. The interaction of seawater with felsic magma and sediments led to the formation of Mg-rich alteration minerals, leaching Si, Fe, Mn and other elements and forming the potential ore fluids. It is highlighted that the A-type alkaline submarine felsic volcanism could be considered as an exploration target for BISF. 相似文献
5.
The Guelb Moghrein copper–gold deposit in the Islamic Republic of Mauritania reopened in 2006 and has produced copper concentrate and gold since then. The deposit is hosted in Neoarchaean–Palaeoproterozoic Fe–Mg carbonate-dominated metamorphic rocks interpreted as carbonate-facies iron formation. It forms tabular orebodies controlled by shear zones in the hanging wall and footwall of this meta-iron formation. Copper and gold are hosted in a complex sulfide ore in tectonic breccia replacing Fe–Mg carbonate and magnetite. Hydrothermal monazite dates the mineralization at 2492 ± 9 Ma. Two types of aqueous fluid inclusions suggest fluid mixing at 0.75–1.80 kbar and ~ 410 °C as the mineralization and precipitation mechanism, which is temporally coincident with regional retrograde metamorphism at 410 ± 30 °C (garnet-biotite). Distal alteration zones are enriched in K, Rb and Cu, whereas orebodies are depleted in K, Rb, Sr and Ba. The copper–gold mineralization at Guelb Moghrein formed during retrograde shearing in metamorphic rocks and contemporaneous hydrothermal alteration. The stable isotope signature of alteration and ore minerals suggest an external crustal fluid source. Fluids were focused in the reactive and competent meta-iron formation. Potassium alteration, magnetite and copper–gold mineralization suggest an IOCG mineral system akin similar deposits in Australia and Brazil. 相似文献
6.
This paper contributes to the understanding of the genesis of epigenetic, hypogene BIF-hosted iron deposits situated in the eastern part of Ukrainian Shield. It presents new data from the Krivoy Rog iron mining district (Skelevatske–Magnetitove deposit, Frunze underground mine and Balka Severnaya Krasnaya outcrop) and focuses on the investigation of ore genesis through application of fluid inclusion petrography, microthermometry, Raman spectroscopy and baro-acoustic decrepitation of fluid inclusions. The study investigates inclusions preserved in quartz and magnetite associated with the low-grade iron ores (31–37% Fe) and iron-rich quartzites (38–45% Fe) of the Saksaganskaya Suite, as well as magnetite from the locally named high-grade iron ores (52–56% Fe). These high-grade ores resulted from alteration of iron quartzites in the Saksaganskiy thrust footwall (Saksaganskiy tectonic block) and were a precursor to supergene martite, high-grade ores (60–70% Fe). Based on the new data two stages of iron ore formation (metamorphic and metasomatic) are proposed.The metamorphic stage, resulting in formation of quartz veins within the low-grade iron ore and iron-rich quartzites, involved fluids of four different compositions: CO2-rich, H2O, H2O–CO2(± N2–CH4)–NaCl(± NaHCO3) and H2O–CO2(± N2–CH4)–NaCl. The salinities of these fluids were relatively low (up to 7 mass% NaCl equiv.) as these fluids were derived from dehydration and decarbonation of the BIF rocks, however the origin of the nahcolite (NaHCO3) remains unresolved. The minimum P–T conditions for the formation of these veins, inferred from microthermometry are Tmin = 219–246 °C and Pmin = 130–158 MPa. The baro-acoustic decrepitation analyses of magnetite bands indicated that the low-grade iron ore from the Skelevatske–Magnetitove deposit was metamorphosed at T = ~ 530 °C.The metasomatic stage post-dated and partially overlapped the metamorphic stage and led to the upgrade of iron quartzites to the high-grade iron ores. The genesis of these ores, which are located in the Saksaganskiy tectonic block (Saksaganskiy ore field), and the factors controlling iron ore-forming processes are highly controversial. According to the study of quartz-hosted fluid inclusions from the thrust zone the metasomatic stage involved at least three different episodes of the fluid flow, simultaneous with thrusting and deformation. During the 1st episode three types of fluids were introduced: CO2–CH4–N2(± C), CO2(± N2–CH4) and low salinity H2O–N2–CH4–NaCl (6.38–7.1 mass% NaCl equiv.). The 2nd episode included expulsion of the aqueous fluids H2O–N2–CH4–NaCl(± CO2, ± C) of moderate salinities (15.22–16.76 mass% NaCl equiv.), whereas the 3rd event involved high salinity fluids H2O–NaCl(± C) (20–35 mass% NaCl equiv.). The fluids most probably interacted with country rocks (e.g. schists) supplying them with CH4 and N2. The high salinity fluids were most likely either magmatic–hydrothermal fluids derived from the Saksaganskiy igneous body or heated basinal brines, and they may have caused pervasive leaching of Fe from metavolcanic and/or the BIF rocks. The baro-acoustic decrepitation analyses of magnetite comprising the high-grade iron ore showed formation T = ~ 430–500 °C. The fluid inclusion data suggest that the upgrade to high-grade Fe ores might be a result of the Krivoy Rog BIF alteration by multiple flows of structurally controlled, metamorphic and magmatic–hydrothermal fluids or heated basinal brines. 相似文献
7.
Tabular–type uranium ore deposits (the Hangjinqi and Daying deposits) have recently been found in the Middle Jurassic Zhiluo Formation, north of the Ordos Basin, China. Petrographic observations, the chemical composition of U minerals determined by EMPA and fs–LA–ICP–MS, whole rock geochemistry and the microthermometric study of fluid inclusions have been integrated to characterize the genetic conditions of the U mineralization in the Hangjinqi sandstone–hosted deposit. Two different groups of U minerals have been identified. One group includes coffinite(I) associated with vanadium–rich micas. Coffinite(I) is enriched in vanadium (V) and devoid of iron (Fe) and yttrium (Y) and has a LREE–enriched chondrite–normalized REE pattern. The U minerals of this group are similar to meteoric fluid infiltration related deposits. The second group has coeval coffinite(II) and coarsely crystalline calcite cement. Coffinite(II) is enriched in Y and Fe and depleted in V and is marked by a flat chondrite–normalized REE pattern, which is compatible with typical hydrothermal genetic deposits with high–salinity mineralizing fluids. The temperature and salinity of the primary aqueous inclusions in the ore–stage calcite are 120–180 °C and 8.00–16.34% (eq. wt% NaCl), respectively. These mineral assemblages, temperatures and salinities indicate that the Hangjinqi deposit was affected by two distinct types of ore–bearing fluids: low–salinity meteoric waters and high–salinity hydrothermal fluids. The meteoric fluids event began at 97 ± 5 Ma with the titling of the northern Ordos Basin and the uplift of the Hetao region to the north. Hydrothermal U mineralization occurred since 39 ± 2 Ma with the rifting of the Hetao graben. Thus, the previous biogenic model for the U mineralization should be modified in the uraniferous region of the north Ordos Basin. 相似文献
8.
Formation of the Urals Volcanic-Hosted Massive Sulphide (VHMS) deposits is considered to be related with the intra-oceanic stage of the island arc(s) development in Late Ordovician – Middle Devonian time (ca. 460–385 Ma) based on the biostratigraphic record of ore-hosting sedimentary rocks. However, the known radiometric ages of ore hosting volcanics are very limited. Here we present direct dating results of sulphide mineralisation from the Yaman-Kasy and Kul-Yurt-Tau VHMS deposits using Re-Os isotope systematics showing similar mineralisation ages of 362 ± 9 Ma and 363 ± 1 Ma. These ages coincide with the previous Re-Os dating of the Alexandrinskoe (355 ± 15 Ma) and Dergamysh (366 ± 2 Ma) VHMS deposits. This Late Devonian (Famennian) age corresponds to the late stage of the ‘Magnitogorsk arc – Laurussia continent’ collision event and coincides with a beginning of large scale subduction-related granitoid magmatism. The younger mineralisation age relative to the biostratigraphic ages of host rocks is interpreted as one of the latest episodes of the multi-stage history of VHMS deposits development. Ar-Ar ages of sericites from metasomatic rocks of Barsuchi Log and Babaryk deposits show even younger ages clustering around 345 Ma, and testify another late hydrothermal event in the history of the Urals VHMS deposits. 相似文献
9.
The Tasiast gold deposits are hosted within Mesoarchean rocks of the Aouéouat greenstone belt, Mauritania. The Tasiast Mine consists of two deposits hosted within distinctly different rock types, both situated within the hanging wall of the west-vergent Tasiast thrust. The Piment deposits are hosted within metasedimentary rocks including metaturbidites and banded iron formation where the main mineral association consists of magnetite-quartz-pyrrhotite ± actinolite ± garnet ± biotite. Gold is associated with silica flooding and sulphide replacement of magnetite in the turbidites and in the banded iron formation units. The West Branch deposit is hosted within meta-igneous rocks, mainly diorites and quartz diorites that lie stratigraphically below host rocks of the Piment deposits. Most of the gold mineralisation at West Branch is hosted by quartz–carbonate veins within the sheared and hydrothermally altered meta-diorites that constitute the Greenschist Zone. At Tasiast, gold mineralisation has been defined over a strike length > 10 km and to vertical depths of 740 m. All of the significant mineralised bodies defined to date dip moderately to steeply (45° to 70°) to the east and have a south–southeasterly plunge. Gold deposits on the Tasiast trend are associated with second order shear zones that are splays cutting the hanging wall block of the Tasiast thrust. An age of 2839 ± 36 Ma obtained from the hydrothermal overgrowth on zircons from a quartz vein is interpreted to represent the age of mineralisation. 相似文献
10.
Numerous Fe-Cu deposits with mineralization styles similar to iron oxide-copper gold (IOCG) deposits form the Kangdian Fe-Cu metallogenic province, southwestern (SW) China. As one of the largest deposits in the region, the ~ 1.0 Ga Lala Fe-Cu deposit is hosted in a Paleoproterozoic volcanic-sedimentary succession named the Hekou Group which is alternately intruded by ~ 1.0 Ga doleritic plutons. This deposit has a paragenetic sequence evolving from Stage I of Na-alteration to Stage II of Fe mineralization, and finally to Stage III of Cu-(Mo, REE) mineralization, coeval with mafic-felsic intra-plate magmatism in the region. This study conducted in-situ Sr isotopic analyses on apatite and carbonate, aiming to resolve the long controversial issue regarding the origin of the Fe and Cu mineralizing fluids in the deposit. Apatite of Stage II has 87Sr/86Sr ratios varying from 0.71380 to 0.72733, much higher than those of synchronous igneous rocks in the region (0.7074 to 0.7091), but similar to the Paleoproterozoic host rocks (0.71368 to 0.71837 at ~ 1.0 Ga). This similarity indicates that radiogenic Sr of the Fe mineralizing fluid was dominantly sourced from the host rocks. Apatite and calcites of Stage III have 87Sr/86Sr ratios (0.75758–0.79293) much higher than apatite of Stage II and the host rocks but similar to the Archean basement rocks (as high as 0.80 at ~ 1.0 Ga) beneath the cover of the Yangtze Block, suggesting that the highly radiogenic Sr isotopic composition of the Cu mineralizing fluid was mainly inherited from the old basement rocks. In combination with previous C-O-S isotopic data indicating a magma-hydrothermal origin, it was suggested that the Fe mineralizing fluid was exsolved from a mafic magma that generated the ~ 1.0 Ga doleritic plutons, and inherited radiogenic Sr from the host rocks during fluid-rock interaction. By contrast, the Cu mineralizing fluid might have been sourced from another pulse of magmatic, Cu-Mo-REE- and CO2-rich fluid which have once interacted with Archean basement rocks prior to mineralization. The source of such a Cu-Mo-REE-rich fluid was not well constrained in current study but was inferred to be exsolved from a hidden felsic magma. We propose that intrusions of the bimodal magmas in Kangdian are responsible for regional hydrothermal circulation which led to Fe-Cu-(Mo, REE) mineralization in the Kangdian province. 相似文献
11.
The Chadormalu is one of the largest known iron deposits in the Bafq metallogenic province in the Kashmar-Kerman belt, Central Iran. The deposit is hosted in Precambrian-Cambrian igneous rocks, represented by rhyolite, rhyodacite, granite, diorite, and diabasic dikes, as well as metamorphic rocks consisting of various schists. The host rocks experienced Na (albite), calcic (actinolite), and potassic (K-feldspar and biotite) hydrothermal alteration associated with the formation of magnetite–(apatite) bodies, which are characteristic of iron oxide copper-gold (IOCG) and iron oxide-apatite (IOA) systems. Iron ores, occurring as massive-type and vein-type bodies, consist of three main generations of magnetite, including primary, secondary, and recrystallized, which are chemically different. Apatite occurs as scattered irregular veinlets in various parts of the main massive ore-body, as well as apatite-magnetite veins and disseminated apatite grains in marginal parts of the deposit and in the immediate wall rocks. Minor pyrite occurs as a late phase in the iron ores. Chemical composition of magnetite is representative of an IOA or Kiruna-type deposit, which is consistent with other evidence.Whole rock geochemical data from various host rocks confirm the occurrence of Na, Ca, and K alteration consistent with the formation of albite, actinolite, and K-feldspar, respectively. The geochemical investigation also includes the nature of calc-alkaline igneous rocks, and helps elaborating on the spatial and temporal association, and possible contribution of mafic to felsic magmas to the evolution of ore-bearing hydrothermal fluids.Fluid inclusion studies on apatites from massive- and vein-type ores show a range of homogenization temperatures from 266 to 580 °C and 208–406 °C, and salinities from 0.5 to 10.7 wt.% and 0.3–24.4 wt.% NaCl equiv., respectively. The fluid inclusion data suggest the involvement of evolving fluids, from low salinity-high temperature, to high salinity-low temperature, in the formation of the massive- and vein-type ores, respectively. The δ34S values obtained for pyrite from various parts of the deposit range between +8.9 and +14.4‰ for massive ore and +18.7 to +21.5‰ for vein-type ore. A possible source of sulfur for the 34S-enriched pyrite would be originated from late Precambrian-early Cambrian marine sulfate, or fluids equilibrated with evaporitic sulfates.Field observations, ore mineral and alteration assemblages, coupled with lithogeochemical, fluid inclusion, and sulfur isotopic data suggest that an evolving fluid from magmatic dominated to surficial brine-rich fluid has contributed to the formation of the Chadormalu deposit. In the first stages of mineralization, magmatic derived fluids had a dominant role in the formation of the massive-type ores, whereas a later brine with higher δ34S contributed to the formation of the vein-type ores. 相似文献
12.
The age and origin of the past-producing Nanisivik carbonate-hosted ZnPb deposit in Nunavut, Canada, have been controversial for decades. Various direct and indirect dating methods have produced results ranging from Mesoproterozoic to Ordovician in age, and previous studies of the mineralising fluids have suggested that the fluids were anomalously hot (> 150 °C). This study combines ReOs (pyrite) geochronology, in-situ sulphur isotope analysis, and fluid inclusion analysis to refine both the timing of mineralisation and the nature of mineralising fluids. ReOs pyrite analysis shows that the Nanisivik deposit formed ca. 1.1 Ga, broadly similar to the depositional age of the host rock and with the Grenville orogeny, making it one of few known Precambrian carbonate-hosted ZnPb deposits. In-situ sulphur isotope measurements from Nanisivik show a narrow δ34S range of 27.54 ± 0.72, very similar to what has been reported before in bulk sample analyses. New fluid inclusion data show that the mineralising fluids were ~ 100 °C, which is not anomalous in the context of carbonate-hosted base-metal deposits. The fluids exhibit no significant spatial variation in homogenisation temperature in the 2-km-long ‘upper lens’ of the ore deposit, but recrystallisation and modification of fluid inclusions took place in the immediate vicinity of the cross-cutting ~ 720 Ma “mine dyke”. The deposit is broadly inferred to have formed during late Mesoproterozoic assembly of supercontinent Rodinia, when regional hydrostatic head developed under the influence of far-field stresses originating in the developing Grenville orogen. The Nanisivik deposit remains anomalous only in its age; most other aspects of this ore deposit are now shown to be quite typical for carbonate-hosted ore deposits. 相似文献
13.
The North China craton hosts numerous iron skarn deposits containing more than 2600 Mt of iron ores, mostly with an average grade of >45 wt% Fe, which have been among the most important source of high-grade iron ores for the last three decades in China. These deposits typically form clusters and can be roughly divided into the western and eastern belts, which are located in the middle of Trans-North China orogen and to the west of the Tan-Lu fault zone in the eastern part of North China craton, respectively. The western belt mainly consists of the southern Taihang district, as well as the Linfen and Taiyuan ore fields, whereas the eastern belt comprises the Luxi and Xu-Huai districts. The Zhangjiawa deposit in the Luxi district has proven reserves of 290 Mt at an average of 46% Fe (up to >65%). The iron mineralization occurs mainly along contact zones between the Kuangshan dioritic intrusion and middle Ordovician marine carbonate rocks that host numerous evaporite intercalations. Titanite grains from the mineralized skarn are closely intergrown with magnetite and retrograde skarn minerals including chlorite, phlogopite and minor epidote, indicating a hydrothermal origin. The titanite grains have extremely low REE contents and low Th/U ratios, consistent with their precipitation directly from hydrothermal fluids responsible for the iron mineralization. Ten hydrothermal titanite grains yield a weighted mean 206Pb/238U age of 131.0 ± 3.9 Ma (MSWD = 0.1, 1σ), which is in excellent agreement with a zircon U-Pb age (130 ± 1 Ma) of the ore-related diorite. This age consistency confirms that the iron skarn mineralization is temporally and likely genetically related to the Kuangshan intrusion. Results from this study, when combined with existing isotopic age data, suggest that iron skarn mineralization and associated magmatism throughout both the eastern and western belts took place coevally between 135 and 125 Ma, with a peak at ca. 130 Ma. As such, those deposits may represent the world's only major Phanerozoic iron skarn concentration hosted in Precambrian cratons. The magmatism and associated iron skarn mineralization coincide temporally with the culmination of lithospheric thinning and destruction of the North China craton, implying a causal link between the two. 相似文献
14.
The Bayan Obo Fe–REE–Nb deposit is the world's largest rare earth element (REE) resource and with the increasing focus on critical metal resources has become a focus of global interest. The deposit is hosted in the Palaeoproterozoic Bayan Obo Group, mainly concentrated in the H8 dolomite marble. The ores consist of light REE enriched monazite and bastnäsite, with a wide array of other REE minerals. Niobium mineralisation is hosted primarily in aeschynite and pyrochlore, although there are a wide range of other Nb-minerals. The origin of the host dolomite and ore bodies has been a subject of intense debate. The host dolomite has been proposed to be both of sedimentary origin and an igneous carbonatite. Carbonatite dykes do occur widely in the area, and consideration of the textural, geochemical and isotopic composition of the dolomite suggests an origin via intrusion of magmatic carbonatite into meta-sedimentary marble, accompanied by metasomatism. The origin of the ore bodies is complex, indicated most strongly by an ~ 1 Ga range in radiometric age determinations. Compilation of available data suggests that the ores were originally formed around 1.3 Ga (Sm–Nd isochron ages; Th–Pb ages of zircon), close in time to the intrusion of the carbonatite dykes. The ores were subsequently subjected to several stages of deformation and hydrothermal overprint, culminating in deformation, metamorphism and fluid flow related to the Caledonian subduction of the Mongolian Plate under the North China Craton from ~ 450 to 420 Ma (Th–Pb ages of monazite). This stage resulted in the formation of the strong foliation (‘banding’) of the ore. The presence of undeformed veins with alkali mineral fills, and the overprinting of the foliation by Nb minerals suggest that secondary fluid flow events may also have contributed to the metal endowment of the deposits, as well as remobilising the original Fe and REE mineralisation. The alteration mineralogy and geochemistry of the ores are comparable to those of many REE mineralised carbonatites. Initial Nd isotope ratios at 450 Ma, however, suggest crustal sources for the metals. These conflicting lines of evidence can be reconciled if a (at least) two stage isotopic evolution is accepted for the deposits, with an original mantle-sourced, carbonatite-related metal accumulation forming around 1.3 Ga with εNd close to 0. The ore was remobilised, with associated re-equilibration of Th–Pb isotope systematics during deformation at ~ 450 Ma. A further stage of alkaline hydrothermal fluid was responsible for Nb mineralisation at this stage. The complex geological history, with multiple stages of alkaline, high field strength element-rich, metasomatic fluid flow, is probably the main reason for the exceptional metal endowment of the Bayan Obo area. 相似文献
15.
Numerous magnetite–apatite deposits occur in the Ningwu and Luzong sedimentary basins along the Middle and Lower Yangtze River, China. These deposits are located in the contact zone of (gabbro)-dioritic porphyries with surrounding volcanic or sedimentary rocks and are characterized by massive, vein and disseminated magnetite–apatite ± anhydrite mineralization associated with voluminous sodic–calcic alteration. Petrologic and microthermometric studies on multiphase inclusions in pre- to syn-mineralization pyroxene and garnet from the deposits at Meishan (Ningwu basin), Luohe and Nihe (both in Luzong basin) demonstrate that they represent extremely saline brines (~ 90 wt.% NaClequiv) that were trapped at temperatures of about 780 °C. Laser ablation ICP-MS analyses and Raman spectroscopic studies on the natural fluid inclusions and synthetic fluid inclusions manufactured at similar P–T conditions reveal that the brines are composed mainly of Na (13–24 wt.%), K (7–11 wt.%), Ca (~ 7 wt.%), Fe (~ 2 wt.%), Cl (19–47 wt.%) and variable amounts of SO4 (3–39 wt.%). Their Cl/Br, Na/K and Na/B ratios are markedly different from those of seawater evaporation brines and lie between those of magmatic fluids and sedimentary halite, suggesting a significant contribution from halite-bearing evaporites. High S/B and Ca/Na ratios in the fluid inclusions and heavy sulfur isotopic signatures of syn- to post-mineralization anhydrite (δ34SAnh = + 15.2 to + 16.9‰) and pyrite (δ34SPy = + 4.6‰ to + 12.1‰) further suggest a significant contribution from sedimentary anhydrite. These interpretations are in line with the presence of evaporite sequences in the lower parts of the sedimentary basins.The combined evidence thus suggests that the magnetite–apatite deposits along the Middle and Lower Yangtze River formed by fluids that exsolved from magmas that assimilated substantial amounts of Triassic evaporites during their ascent. Due to their Fe-oxide dominated mineralogy, their association with large-scale sodic–calcic alteration and their spatial and temporal associations with subvolcanic intrusions we interpret them as a special type of IOCG deposits that is characterized by unusually high contents of Na, Ca, Cl and SO4 in the ore-forming fluids. Evaporite assimilation apparently led to the production of large amounts of high-salinity brine and thus to an enhanced capacity to extract iron from the (gabbro)-dioritic intrusions and to concentrate it in the form of ore bodies. Hence, we believe that evaporite-bearing sedimentary basins are more prospective for magnetite–apatite deposits than evaporite-free basins. 相似文献
16.
The magnetite deposits of the Turgai belt (Kachar, Sarbai and Sokolov), in the Valerianovskoe zone of the southern Urals, Kazakhstan, contain a combined resource of over 3 Gt of iron oxide ore. The deposits are hosted by carbonate sediments and volcaniclastic rocks of the Carboniferous Valerianovka Supergroup, and are spatially related to the gabbroic to granitoid composition intrusive rocks of the Sarbai–Sokolov intrusive series. The magnetite deposits are developed dominantly as metasomatic replacement of limestone, but also, to a lesser extent, of volcanic rocks. Pre-mineralisation metamorphism and alteration resulted in the formation of wollastonite and the silicification of limestone. Magnetite mineralisation is associated with the development of a high temperature skarn assemblage of diopside, grossular–andradite garnet, actinolite, epidote and apatite. Sub-economic copper-bearing sulphide mineralisation overprints the magnetite mineralisation and is associated with deposition of hydrothermal calcite and the formation of an extensive sodium alteration halo dominated by albite and scapolite. Chlorite formation accompanies this stage and further later stage hydrothermal overprints. The replacement has in places resulted in preservation of primary features of the limestone, including fossils and sedimentary structures in magnetite, skarn calc-silicates and sulphides.Analysis of Re–Os isotopes in molybdenite indicates formation of the sulphide mineral assemblage at 336.2 ± 1.3 Ma, whilst U–Pb analyses of titanite from the skarn alteration assemblage suggests skarn alteration at 326.6 ± 4.5 Ma with re-equilibration of isotope systematics down to ~ 270 Ma. Analyses of mineral assemblages, fluid inclusion microthermometry, O and S isotopes suggest initial mineralisation temperatures in excess of 600 °C from hypersaline brines (45–50 wt.% NaCl eq.), with subsequent cooling and dilution of fluids to around 150 °C and 20 wt.% NaCl eq. by the time of calcite deposition in late stage sulphide-bearing veins. δ18O in magnetite (− 1.5 to + 3.5‰) and skarn forming silicates (+ 5 to + 9‰), δ18O and δ13C in limestone and skarn calcite (δ18O + 5.4 to + 26.2‰; δ13C − 12.1 to + 0.9‰) and δ34S in sulphides (− 3.3 to + 6.6‰) and sulphates (+ 4.9 to + 12.9‰) are all consistent with the interaction of a magmatic-equilibrated fluid with limestone, and a dominantly magmatic source for S. All these data imply skarn formation and mineralisation in a magmatic–hydrothermal system that maintained high salinity to relatively late stages resulting in the formation of the large Na-alteration halo. Despite the reported presence of evaporites in the area there is no evidence for evaporitic sulphur in the mineralising system.These skarns show similarities to some members of the iron oxide–apatite and iron oxide–copper gold deposit classes and the model presented here may have implications for their genesis. The similarity in age between the Turgai deposits and the deposits of the Magnitogorsk zone in the western Urals suggests that they may be linked to similar magmatism, developed during post-orogenic collapse and extension following the continent–continent collision, which has resulted in the assembly of Laurussian terranes with the Uralide orogen and the Kazakh collage of the Altaids or Central Asian Orogenic Belt. This model is preferred to the model of simultaneous formation of very similar deposits in arc settings at either side of an open tract of oceanic crust forming part of the Uralian ocean. 相似文献
17.
South China Block (SCB) is the broad area including the Yangtze Craton in the northwest and Huanan Orogen in the southeast. It is an important epithermal metallogenic province in China, containing at least 1 high-sulfidation (HS) and 42 low-sulfidation (LS) Au-Ag ± Cu ± Pb-Zn ± Sb epithermal deposits. Porphyry-type mineralization was recognized in four of the LS deposits, and thus they were regarded as LS–P type. These 43 deposits are mainly located in: (1) the Lower Yangtze River Belt and (2) the Northeastern Jiangnan Orogenic Belt in the Yangtze Craton, (3) the Wuyi-Yunkai Orogenic Belt and (4) the Southeast Coastal Volcanic Belt in the Huanan Orogen. They are mostly located in Mesozoic volcanic basins, especially where the regional faults and their subsidiaries occurred. The host rocks include Jurassic–Cretaceous volcanic-sedimentary rocks, coeval or slightly older subvolcanic, granitoids and breccias, and metamorphic basement rocks. The alteration of the HS epithermal deposit (Zijinshan Cu-Au) zoned from silicic (vuggy quartz), through alunite, to dickite and phyllic alteration zones, from the ore veins outwards. The alteration of the LS deposits is zoned from adularia-chalcedony-bladed calcite (or quartz pseudomorphs after bladed calcite) in ore veins to distal illite-sericite-chlorite-kaolinite assemblages. For those LS–P systems, besides the dominated LS alteration assemblages, phyllic and potassium silicate alteration related to porphyry mineralization were identified. Acid leaching textures and vein, stockwork and breccia structures are common in HS deposit, while the LS epithermal deposits are characterized by open-space filling, crustifications, colloform banding and comb structures. The ore-forming fluids are low-temperature, low-salinity meteoric water-dominated in most epithermal deposits in SCB, with variable input of magmatic water. The ore components were derived from both the deep magma and host rocks, and transported upwards or laterally and precipitated in the fracture systems by fluid boiling, mixing and cooling. Most of the epithermal deposits are formed at depth of < 1.5 km and < 300 °C, with few exceptions containing porphyry-type mineralization, such as the Zhilingtou, Yinshan and Longtoushan deposits. Deep drilling is suggested in these deposits as more epithermal and/or porphyry mineralization could be expected. The mineral systems were formed in Early Yanshanian (180–130 Ma) and Late Yanshanian (120–90 Ma) periods. The Early Yanshanian epithermal ore systems are mainly located in a series of E–W-trending metallogenic belts to the west of the Lishui–Haifeng Fault, which were formed in a syn- or post-collision tectonic setting by the collision between the SCB and its surrounding plates. The Late Yanshanian epithermal deposits are mainly located in Southeast Coastal Volcanic Belt, genetically related to the westward subduction of the paleo-Pacific plate. 相似文献
18.
A fundamentally distinct, sulfide-poor variant of intense acid (advanced argillic) alteration occurs at the highest structural levels in iron oxide-rich hydrothermal systems. Understanding the mineralogy, and geochemical conditions of formation in these sulfide-poor mineral assemblages have both genetic and environmental implications. New field observations and compilation of global occurrences of low-sulfur advanced argillic alteration demonstrates that in common with the sulfide-rich variants of advanced argillic alteration, sulfide-poor examples exhibit nearly complete removal of alkalis, leaving a residuum of aluminum-silicate + quartz. In contrast, the sulfur-poor variants lack the abundant pyrite ± other sulfides, hypogene alunite, Al-leached rocks (residual “vuggy” quartz) as well as the Au-Cu-Ag ± As-rich mineralization of some sulfur-rich occurrences. Associated mineralization is dominated by magnetite and/or hematite with accessory elements such as Cu, Au, REE, and P. These observations presented here indicate there must be distinct geologic processes that result in the formation of low-sulfur advanced argillic styles of alteration.Hydrolysis of magmatic SO2 to sulfuric acid is the most commonly recognized mechanism for generating hypogene advanced argillic alteration, but is not requisite for its formation. Low sulfur iron-oxide copper-gold systems are known to contain abundant acid-styles of alteration (e.g. sericitic, chloritic), which locally reaches advanced argillic assemblages. A compilation of mapping in four districts in northern Chile and reconnaissance observations elsewhere show systematic zoning from near surface low-sulfide advanced argillic alteration through chlorite-sericite-albite and locally potassic alteration. The latter is commonly associated with specular hematite-chalcopyrite mineralization. Present at deeper structural levels are higher-temperature styles of sodic-calcic (oligoclase/scapolite – actinolite) alteration associated with magnetite ± chalcopyrite mineralization. These patterns are in contrast to the more sulfur-rich examples which generally zone to higher pyrite and locally alunite-bearing alteration.Fluid inclusion evidence from the systems in northern Chile shows that many fluids contain 25 to >50 wt% NaCleq with appreciable Ca, Fe, and K contents with trapping temperatures >300 °C. These geological and geochemical observations are consistent with the origin of the low-sulfur advanced argillic assemblages from HCl generated by precipitation of iron oxides from iron chloride complexes from a high-salinity fluid by reactions such as 3FeCl2 + 4H2O = Fe3O4 + 6HCl + H2. Such HCl-rich (and relatively HSO4=-poor) fluids can then account for the intense acid, Al-silicate-rich styles of alteration observed at high levels in some iron-oxide-coppe-gold (IOCG) systems. The geochemical differences between the presence of sulfide-rich and sulfur-poor examples of advanced argillic alteration are important to distinguishing between system types and the acid-producing capacity of the system, including in the modern weathering environment. They have fundamental implications for effective mineral exploration in low-sulfur systems and provide yet another vector of exposed alteration in the enigmatic IOCG clan of mineral deposits. Furthermore, understanding the geochemistry and mineralogy of this distinct geologic environment has applications to understanding the acid generating capacity and deleterious heavy metals associated with advanced argillic alteration. 相似文献
19.
Stratabound massive sulfide deposits are widespread along the Middle-Lower Yangtze Metallogenic Belt (MLYMB) and serve as an important copper producer in China. Two contrasting genetic models have been proposed, interpreting the stratabound massive sulfide deposits as a Carboniferous SEDEX protore overprinted by Cretaceous magmatic-hydrothermal system or an Early Cretaceous carbonate replacement deposit. These two contrasting models have been applied to the Xinqiao stratabound Cu-Au sulfide deposit, which is dominated by massive sulfide ores hosted in marine carbonates of the Carboniferous Chuanshan and Huanglong Formations, with minor Cu-Au skarn ores localized in the contact zone between the Cretaceous diorite Jitou stock and the Carboniferous carbonate rocks. New SIMS zircon U-Pb dating suggests that the Jitou stock formed at 138.5 ± 1.1 Ma (2σ, MSWD = 0.6). Pyrite Re-Os dating yields an imprecise date of 142 ± 47 Ma (2σ, MSWD = 7.8). The geochronological data thus constrain the mineralization of the Xinqiao deposit at Early Cretaceous.Fluid inclusions in prograde skarn diopside have homogenization temperatures of 450–600 °C and calculated salinities of 13–58 wt.% NaCl equiv. Quartz from the stratabound ores and pyrite-quartz vein networks beneath the stratabound ores have homogenization temperatures of 290–360 and 200–300 °C, with calculated salinities of 5–12 and 2–10 wt.% NaCl equiv., respectively. Quartz from the skarn ores and veins beneath the stratabound ores have δ18O values of 12.32 ± 0.55 (2 SD, n = 22) and 15.57 ± 1.92‰ (2 SD, n = 60), respectively, corresponding to calculated δ18O values of 6.22 ± 1.59 (2σ) and 6.81 ± 2.76‰ (2σ) for the equilibrated ore-forming fluids. The fluid inclusion and oxygen isotope data thus support a magmatic-hydrothermal origin rather than a SEDEX system for the stratabound ores, with the hydrothermal fluids most likely being derived from the Jitou stock or associated concealed intrusion. Results from this study have broad implications for the genesis and exploration of other stratabound massive sulfide deposits along the MLYMB. 相似文献
20.
The Monakoff iron oxide–Cu–Au (IOCG) deposit, located to the north east of Cloncurry within the Eastern Succession of the Mount Isa Inlier, Queensland, Australia, is characterised by high concentrations of F and Ba, with a host of other enriched elements including Co, Ag, Mn, REE, U, Pb, Zn and Sr. This gives the deposit a characteristic gangue assemblage dominated by fluorite, barite and calcite. The nearby E1 deposit, located 25 km to the NNE of Monakoff, and the large Ernest Henry deposit, 3 km to the west of E1, also contain abundant fluorite, barite and calcite in late stage assemblages. The three deposits, therefore, constitute a distinct group of IOCG deposits within the district, based on their F-rich geochemical and mineralogical affinities.The Monakoff ore zone is hosted in dilational openings along a shear zone developed within metasediments and metavolcanic rocks at the boundary between competent hangingwall rocks of the Toole Creek Volcanics and footwall rocks of the Mount Norna Quartzites. Four stages of alteration and mineralisation are recognised: Stage 1 garnet–biotite alteration; Stage 2 biotite–magnetite alteration; Stage 3 main F–Ba-ore mineralisation; and a Stage 4 pyrite–alloclasite Au–Co–As overprint. The E1 deposit has a more complex history, but Stage 5 has veins of fluorite–barite–carbonate that are comparable to Monakoff's main stage. The Stage 3 assemblage at Monakoff comprises a sheared groundmass of fluorite, barite, manganoan calcite, magnetite, chalcopyrite, pyrite, galena and sphalerite, with coarser grained pods of the same mineralogy interpreted to be dilational structures infilled during syn-ore deformation. Accessory minerals include U–Pb-oxides, REE–F-carbonates and Ag–Pb–Bi-sulfosalts, with no discrete Au minerals. The sulfosalts are interpreted to have formed from an immiscible Bi-melt within the mineralising fluid at temperatures higher than the melting point of Bi. The Stage 4 overprint at Monakoff contains pyrite and alloclasite. Laser ablation analyses of the sulphide minerals at Monakoff reveal that Stage 3 sulphides contain only trace amounts of Au (0.04 ppm in pyrite), although galena and chalcopyrite contain significant concentrations of Ag. Stage 4 pyrite and alloclasite, however, contain ~ 1 ppm Au in solid solution and mass balance calculations indicate the majority of bulk rock Au to be present in these minerals, although the majority of bulk Ag is present in Stage 3 sulphides. The Stage 5 veins at E1 have an identical gangue and accessory mineralogy to Stage 3 at Monakoff and differ in the sulphide mineralogy only in the lack of galena and sphalerite.Four fluid inclusion populations are identified within the fluorite at Monakoff: Group 1 is CO2 rich; Group 2 is complex solid–liquid–vapour inclusions, with two groups based on homogenisation temperature (> 450 °C and 300–375 °C). Laser ablation-ICP-MS analyses indicate that these inclusions contain Cu, Pb, Zn, Fe, Mn, Mg, Ag, REE, U and Ba, but significantly no S, Se or Au; Group 3 are solid–liquid–vapour inclusions with a Th of 200–275 °C, and contain Ba, Na, Mg, K and Br; and Group 4 are low salinity liquid–vapour inclusions. Group 1, 2 and 4 inclusions are also present in fluorite at E1. The REE geochemistry of fluorite from Monakoff and E1 is comparable and is characterised by a distinct positive Eu anomalies in all analyses, interpreted to indicate oxidising conditions at the time of high temperature ore deposition. The presence of abundant fluorite and barite is indicative of fluid mixing due to the insolubility of barite and fluorite and thus Ba and S, and Ca and F must have been introduced via different fluids. We propose that the oxidised fluid represented by the Group 2 inclusions and containing F, Ba, REE, U and base metals, mixed with a reduced, S-bearing fluid in a zone of dilation in the host shear zone that acted as a conduit for fluid flow during D3 deformation. The source of the metal and F-rich fluid is likely to be the nearby granitic intrusions of the Williams–Naraku batholith, probably the Malakoff granite. This granite is also likely to be the source of the CO2 represented by Group 1 fluid inclusions, and the REE, U, base metals and possibly Au, although the high Pb and Zn content of Monakoff and not E1 may suggest a local input of those elements at Monakoff. Stage 4 mineralisation overprints the F–Ba stage and is characterised by a Co–As–Au signature. At present it is unclear if this is a late stage, more reduced, evolution of the main ore fluid, or a separate mineralising event entirely.The presence of this F–Ba-metal-rich fluid has produced a distinctive style of IOCG mineralisation in the area to the north of Cloncurry. The probable link to the Malakoff granite implies that similar deposits may be present within several kilometres of the granite in suitable structural traps. Monakoff illustrates that although structurally controlled, the presence of Na–Ca alteration and ‘red rock’ K-alteration and brecciation are not key exploration criteria for these deposits. In addition, the presence of the overprinting As–Co–Au assemblage may indicate that this is a separate mineralising episode that may be present at other localities in the district. This study has also shown that fluorite can provide a powerful tool for determining ore forming conditions in F-rich IOCG systems. 相似文献