http://www.sciencedirect.com/science/article/pii/S1674987110000125

<正>Carbonatites are commonly related to the accumulation of economically valuable substances such as REE.Cu,and P.The debate over the origin of carbonatites and their relationship to associated silicate rocks has been ongoing for about 45 years.Worldwide,the rocks characteristically display more geochemical enrichments in Ba,Sr and REE than sedimentary carbonate rocks.However,carbonatite's geochemical features are disputed because of secondary mineral effects.Rock-forming carbonates from carbonatites at Qinling.Panxi region,and Bayan Obo in China show REE distribution patterns ranging from LREE enrichment to flat patterns.They are characterized by a Sr content more than 10 times higher than that of secondary carbonates.The coarse- and fine-grained dolomites from Bayan Obo H8 dolomite marbles also show similar high Sr abundance,indicating that they are of igneous origin.Some carbonates in Chinese carbonatites show REE(especially HREE) contents and distribution patterns similar to those of the whole rocks.These intrusive carbonatites display lower platinum group elements and stronger fractionation between Pt and Ir relative to high-Si extrusive carbonatite.This indicates that most intrusive carbonatites may be carbonate cumulates.Maoniuping and Daluxiang in Panxi region are large REE deposits.Hydrothermal fluorite ore veins occur outside of the carbonatite bodies and are emplaced in wallrock syenite.The fiuorite in Maoniuping has Sr and Nd isotopes similar to carbonatite.The Daluxiang fiuorite shows Sr and REE compositions different from those in Maoniuping.The difference is reflected by both the carbonatites and rock-forming carbonates,indicating that REE mineralization is related to carbonatites.The cumulate processes of carbonate minerals make fractionated fluids rich in volatiles and LREE as a result of low partition coefficients for REE between carbonate and carbonatite melt and an increase from LREE to HREE.The carbonatite-derived fluid has interacted with wallrock to form REE ore veins.The amount of carbonatite dykes occurring near the Bayan Obo orebodies may support the same mineralization model,i.e.that fluids evolved from the carbonatite dykes reacted with H8 dolomite marble,and thus the different REE and isotope compositions of coarse- and fine-grained dolomite may be related to reaction processes.     

Thermodynamic Modelling of Ore-Forming Mechanism of the Changkeng Gold-Silver Deposits in Guangdong Province

The Changkeng gold-silver deposits consist of a sediment-hosted, disseminated gold deposit and a replacement-type silver deposit. The mineralizations of gold and silver are zoned and closely related to the silicification of carbonate and clastic rocks, so that siliceous ores dominate in the deposit. The mineralizing temperature ranges mainly from 300 to 170℃, and K+, Na+, Ca2+, Mg2+, and Cl- are the major ions in the ore-forming fluid. Calculations of distribution of metal complexes show that gold is mainly transported by hydrosulphide complexes, but chloride complexes of silver, iron, lead, and zinc, which are transformed into hydroxyl and hydrosulphide complexes under neutral to weak-alkaline circumstances in the late stage, predominate in the ore-forming solutions. Water-rock interaction is confirmed to be the effective mechanism for the formation of silver ores by computer modelling of reaction of hydrothermal solution with carbonate rocks. The solubility analyses demonstrate that the precipitation     

Petrology and Petrogenesis of the Eclogite in Mt.Dabie Area,Central China

The occurrence,mineralogy and geochemistry of eclogites in the Mt.Dabie area show that they were subjected to a high-pressure metamorphism together with the country rocks,but their petrochemistry and REE geochemistry show some difference from those of the country rocks.The geochemical characteristics of the eclogites are similar to those of bot continental tholeiitic basalt and oceanic tholeiitic basalt.The rocks probably subducted to the upper mantle with the Dabie metamorphic complex.When elevated to the surface,they were subjected to different staes of retrogressive metamorphism.     

A comparison between heavy metals released from soil and its efficient speciation extracted by sequential extraction procedure

A simulating experiment was carried out on the interaction between natural precipitation and soil. The results demonstrated that the contents of heavy metals （V, Co, Cr, and Ni） released from soil into the solution under Earth＇s surface conditions are higher than the contents of those metals bonded to exchangeable species, which were extracted by sequential extraction procedure recommended by Tessier and others in 1979. It is demonstrated that the metals bonded to other 3 species （carbonate, Fe-Mn oxide, and organic matter） except those bonded to the exchangeable species in efficient speciation can be released under the Earth＇s surface conditions, when pH=4 in the reaction system, and the higher correlation coefficient indicated that the concentrations of heavy metals released from soil into the solution vary approximately with reaction time in terms of index regulations.     

REE Geochemistry of Sulfides from the Huize Zn-Pb Ore Field, Yunnan Province： Implication for the Sources of Ore-forming Metals

REE abundances in sulfides from the Huize Zn-Pb ore field were determined with the ICPMS after preconcentration. The REE abundances in 26 sulfide samples （including pyrite, galena and sphalerite） are very low, with the ~REE ranging from 1.6×10^-9 to 166.8×10^-9. Their LREE/HREE ratios range from 7.6 to 98, showing LREE enrichment relatively. The JEu values are below 1, indicating that they were deposited from an Eu-depleted and reducing fluid-system. Similar to the ore-hosting carbonate strata, calcite separates from carbonate veinlets filling in the fractures or faults crosscutting the carbonate strata also show clear Eu-depletion. This indicates that the carbonate veinlets and their parent fluid was possibly sourced from the strata and inherited the REE geochemical features of the strata. Therefore, REE-geochemical characteristics of both the sulfides and calcites, which were deposited from an ore-forming hydrothermal system, are similar to those of carbonate strata, and strongly suggest that the ore metals were mainly sourced from carbonate strata.     

REE Abundaces in Megacrysts and Host Basalts：REE Behavior of Magma at High Pressures

Based on REE abundances in megacrysts and host basalts and their equilibrium conditions,it has proved that megacrysts may have been produced from the magma derived from the host rocks or of more basic composition.The REE ratios of megacrysts to host rocks may be taken as partition coefficients when both are equilibrium with each other.The crystal fractionation of megacrysts has caused the evolution of REE in the magma.It is obvious that some host basalts are the product of magma evolution after crystal fractionation.According to REE abundances in the host rocks and the partition coefficients between crystal and liquid,the history of crystal fractionation of magma can be traced.     

Geochemistry of the Rare Earth Elements in Natural Terrestrial Waters：A Review of What Is Currently Knows

The range of observed chemical compositions of natural terrestrial waters varies greatly especially when compared to the essentially constant global composition of the oceans.The concentrations of the REEs in natural terrestrial waters also exhibit more variation than what was reported in seawater,In terrestrial waters ,pH values span the range from acid up to alkaline,In addition,terrestrial waters can range from very dilute waters through to highly concentrated brines.The REE concentrations and their behavior in natural terrestrial waters reflect these compositional ranges,Chemical weathering of rocks represents the source of the REEs to natural terrestrial waters and ,consequently,the REE signature of rocks can impart their REE signature to associated waters,In addition,Because of the typical low solubilities of the REEs both surface and solution complexation can be important in fractionating REEs in aqueous solution.Both of these processes are important in all natural terrestrial waters,however,their relative importance varies as a function of the overall solution composition,In alkaline waters,for example,Solution complexation of the REEs with carbonate ions appears to control their aqueous distributions whereas in acid waters,the REE signature of the labile fraction of the REEs is readily leached from the rocks.In circumneutral pH waters,both processes appear to be important and their relative significance has not yet been determined.     

The Mobility of Rare—Earth Elements During Hydrothermal Activity：A Review

The mobility of the rare-earth elements(REE)during hydrothermal activities is increasingly documented.Geological and experimental evidence suggests that REE may be mobile in solutions rich in F^-,Cl^-,HCO3^-,CO^2- 3,HPO4^2-,PO4^3-,or in combinations of the above ligands,even though little has been known about which ligand or which combination is most effective in mobilizing REE. The fractionation of REE resulting from hydrothermal activities is inconsistent.One set of field data implies the prererential mobility of the light rare-earth elements(LREE).whereas another set of field observations indicates the dominant mobilization of the heavy rare earth elements(HREE),and some theoretical prediction is comtradictory to the field evidence.The Eu anomalies due to hydrothermal activities are complex and plausible explanation is not available.The existing experimental approaches dealing with REE are not adequate for explanation ofREE behaviour in aqueous solutions.Systematic experimental approaches are suggested.     

The role of carbonate-fluoride melt immiscibility in shallow REE deposit evolution

The Lugiin Gol nepheline syenite intrusion, Mongolia, hosts a range of carbonatite dikes mineralized in rare-earth elements(REE). Both carbonatites and nepheline syenite-fluorite-calcite veinlets are host to a previously unreported macroscale texture involving pseudo-graphic intergrowths of fluorite and calcite. The inclusions within calcite occur as either pure fluorite, with associated REE minerals within the surrounding calcite, or as mixed calcite-fluorite inclusions, with associated zirconosilicate minerals. Consideration of the nature of the texture, and the proportions of fluorite and calcite present(～29 and 71 mol%,respectively), indicates that these textures most likely formed either through the immiscible separation of carbonate and fluoride melts, or from cotectic crystallization of a carbonatefluoride melt. Laser ablation ICP-MS analyses show the pure fluorite inclusions to be depleted in REE relative to the calcite. A model is proposed, in which a carbonate-fluoride melt phase enriched in Zr and the REE, separated from a phonolitic melt, and then either unmixed or underwent cotectic crystallization to generate an REE-rich carbonate melt and an REE-poor fluoride phase. The separation of the fluoride phase(either solid or melt) may have contributed to the enrichment of the carbonate melt in REE, and ultimately its saturation with REE minerals. Previous data have suggested that carbonate melts separated from silicate melts are relatively depleted in the REE, and thus melt immiscibility cannot result in the formation of REE-enriched carbonatites. The observations presented here provide a mechanism by which this could occur, as under either model the textures imply initial separation of a mixed carbonate-fluoride melt from a silicate magma. The separation of an REEenriched carbonate-fluoride melt from phonolitic magma is a hitherto unrecognized mechanism for REE-enrichment in carbonatites, and may play an important role in the formation of shallow magmatic REE deposits.     

Characteristics of rare-earth elements （REE）, strontium and neodymium isotopes in hydrothermal fluorites from the Bailashui tin deposit in the Furong ore field,southern Hunan Province,China

In this paper the authors present the REE concentrations and Sr and Nd isotopic compositions of fluorites from the Bailashui tin deposit of the Furong ore field, southern Hunan Province. The results showed that the total amount of REE in fluorites is usually low, ranging from 0.705 to 8.785 μg/g with the chondrite-normalized REE distribution patterns similar to those of the Qitianling granites in the study area, characterized by LREE-enrichment patterns with pronounced negative Eu anomalies. The fluorites vary in Sr isotopic composition within the range of 0.7083-0.7091, the values are lower than those of the granites and higher than those of the host carbonate rocks in this area. The εNd（t） values of fluorites vary between -9.4 and ＋10.3, revealing that both the crust- and mantle-source materials were involved in the ore-forming hydrothermal fluids. Combined with previous studies on this ore deposit, the Bailashui tin deposit is temporally and spatially closely related with granitic magmatism in this area. The hydrothermal fluorites are the product of fluid/rock interactions between granitic magmatic hydrothermal fluid and marine carbonate rocks. The REE and F in the ore-forming fluid were derived from the granites, whereas Sr in the ore-forming fluid came mainly from the granitic magmatic hydrothermal fluid and marine carbonate rocks, although variations in Sr isotopic composition cannot be explained by a simple mixture of these two end-members. Evidence demonstrated that the ore-forming fluids are of crustal-mantle mixing origin, but that the fluids were probably incompletely homogenized and this may be caused by inhomogeneous mixing of the fluids of different sources.     

The geochemical characteristics of aqueous rare-earth elements in shallow karst groundwater in Guiyang City,China

Fifty-seven shallow groundwater samples were collected from Guiyang karst basin, China, to analyze the aqueous rare-earth elements in low-water seasons and it is shown that the total amount of rare-earth elements (ΣREE) in karst groundwater is exceedingly low compared with that in carbonate rocks or weathering crusts of carbonate rocks, and ranges from 0.01 to 0.43, from 0.03 to 0.27, from 0.03 to 0.19 and from 0.05 to 1.38 μg·L-1 for dolomite, dolomitic & limestone, limestone and clastic rock aquifer, respectively. Both distributions and contents of rare-earth elements (REE) in karst groundwater reflect the lithology of host rocks or weathering crusts of carbonate rocks through which groundwater flows. The chondrite-normalized patterns show a non-flat profile with higher enrichment of slightly light rare-earth elements (LREE) than heavy rare-earth elements (HREE), prominent fractionation between LREE and HREE, negative Ce anomalies and negative or positive Eu anomalies. There is more obvious fractionation between LREE and HREE in groundwater than that in carbonate rocks and their weathering crusts due to high contents of HCO3? and PH in groundwater. In shallow karst groundwater, REE(CO3)n2n-3 (n=1 and 2) is the main inorganic species of REE. But for a clastic rock aquifer, both REESO4+ and REECO3+ are the main inorganic species of REE. Species of REE in groundwater is closely associated with the hydrochemical type of groundwater which is predominated by the lithology of host rocks, groundwater-rock interaction and weathering-pedogenesis of carbonate rocks.     

Raman and infrared spectroscopic quantification of the carbonate concentration in K2CO3 aqueous solutions with water as an internal standard

Carbonate-bearing fluids widely exist in different geological settings,and play important roles in transporting some elements such as the rare earth elements.They may be trapped as large or small fluid inclusions(with the size down to<1μm sometimes),and record critical physical-chemical signals for the formations of their host minerals.Spectroscopic methods like Raman spectroscopy and infrared spectroscopy have been proposed as effective methods to quantify the carbonate concentrations of these fluid inclusions.Although they have some great technical advantages over the conventional microthermometry method,there are still some technical difficulties to overcome before they can be routinely used to solve relevant geological problems.The typical limitations include their interlaboratory difference and poor performance on micro fluid inclusions.This study prepared standard ion-distilled water and K₂CO₃aqueous solutions at different molarities(from 0.5 to 5.5 mol/L),measured densities,collected Raman and infrared spectra,and explored correlations between the K₂CO₃molarity and the spectroscopic features at ambient P-T conditions.The result confirms that the Raman O-H stretching mode can be used as an internal standard to determine the carbonate concentrations despite some significant differences among the correlations,established in different laboratories,between the relative Raman intensity of the C-O symmetric stretching mode and that of the O-H stretching mode.It further reveals that the interlaboratory difference can be readily removed by performing one high-quality calibration experiment,provided that later quantifying analyses are conducted using the same Raman spectrometer with the same analytical conditions.Our infrared absorption data were collected from thin fluid films(thickness less than~2μm)formed by pressing the prepared solutions in a Microcompression Cell with two diamond-II plates.The data show that both the O-H stretching mode and the O-H bending mode can be used as internal standards to determine the carbonate concentrations.Since the IR signals of the C-O antisymmetric stretching vibration of the CO32
ion,and the O-H stretching and bending vibrations from our thin films are very strong,their relative IR absorbance intensity,if well calibrated,can be used to investigate the micron-sized carbonate-bearing aqueous fluid inclusions.This study establishes the first calibration of this kind,which may have some applications.Additionally,our spectroscopic data suggest that as the K₂CO₃concentration increases the aqueous solution forms more large water molecule clusters via more intense hydrogen-bonding.This process may significantly alter the physical and chemical behavior of the fluids.     

碳酸盐矿物的包裹有机质及其生油意义

Fluorescent slice observations have revealed a considerable amount of organic matter enclosed in carbonate minerals, most of it giving off yellow-brown fluorescence and being zonally distributed in calcite and dolomite. The amount of enclosed organic matter released from the enclosure when treated with HCl is two times higher than that of extractable organic mattes in the same rock sample. In comparison to the extractable organic matter, the enclosed organic matter is possessed of some compositional characters of its own. In terms of the distribution of biological markess, it is suggested that the enclosed organic matter may be low in maturity relative to the extractable organic matter in the same source rock.Results of the simulating experiments under high temperatures and pressures show that this kind of organic matter enclosed in carbonate minerals can be converted into oil-generating substances. Therefore, detailed studies of the enclosed organic matter are of much help to the evaluation of oil-generating potentiality of carbonate source rocks.     

Geochemical characteristics and geological significance of the Neoproterozoic carbonates from northern Anhui Province,China

Petrographical and geochemical studies were carried out of the Neoproterozoic carbonates from northern Anhui Province, China. These carbonates can be subdivided into two types, including purified limestone (PL) and mixed limestone and siliclastic rocks (MLS). PLs are low in Si, Al, Zr and total REE but high in CaO compared with MLSs. Correlations between Zr, Fe2O3, P2O5 and total REE are also less remarkable, indicating that they were not obviously contaminated by continental materials but directly precipitated from seawater. So they can be used for the inversion of paleo-seawater REE patterns. The inversed results indicated that the REE pattern of Neoproterozoic seawater was similar to that of the modern seawater except for the lack of Ce depletion, which was probably affected by the reduced hydrothermal solution. In combination with previous studies, the geochemical trending of these carbonatic samples towards the continental arc in the La- Th-Sc and Th-Sc-Zr/10 diagrams is interpreted as the contamination of arc volcanism. The tectonic background of the southern margin of the North China Craton in the Neoproterozoic was probably related to the Grenville orogeny during the convergence of the Rodinia supercontinent, rather than an intra-plate environment.     

An experimental study on the effects of microbes on the migration and accumulation of REE in the weathering crust of granite

Microbes were cultured and identified from the saples collected at various depths in 4 weathering profiles of REE-bearing granites in Gonghe,Guangdong,The microbes were found existing at the depth of 0-5m in all the profiles.The main microbes include coccus (Staphylococcus,Streptococcus),bacillus(Bacillus,Clostridium and Escherichia Coli),actinmyces and fungi(Saccharomycete,Penicillium,Fusarium,Aspergillus Aiger and Mucor),The number of colonies decreases downwards in the profiles.Experimental studies show that all the microbes used in the experiment can accelerate downward migation of REE in the experimental tubes.,The ability to accelerate the migration of REE decreases in a sequence of fungi→actinomyces→acillus→coccus.The microbes can change the modes of occurrence of REE in the weathering crust.The coccus,bacillus and actinomyces can increase the amounts of REE in ion state,whereas the fungi have a stronger ability to from organic compounding REE and accumulate REE than the bacteria do.     

Geology and Genesis of the Superlarge Jinchang Gold Deposit, NE China

The superlarge Jinchang gold deposit is located in the joint area between the Taipingling uplift and the Laoheishan depression of the Xingkai Block in both eastern Jilin and eastern Heilongjiang Province. Wall rocks of the gold deposits are the Neoproterozoic Huangsong Group of metamorphic rocks. Yanshanian magmatism in this region can be divided into 5 phases, the diorite, the graphic granite, the granite, the granite porphyry and the diorite porphyrite, which resulted in the magmatic domes and cryptoexplosive breecia chimney followed by large-scale hydrothermal alteration. Gold mineralization is closely related to the fourth and fifth phase of magmatism. According to the occurrences, gold ores can be subdivided into auriferous pyritized quartz vein, auriferous quartz-pyrite vein, auriferous polymetailic sulfide quartz vein and auriferous pyritized calcite vein. The ages of the gold deposit are ranging from 122.53 to 119.40 Ma. The ore bodies were controlled by a uniform tectono-magmatic hydrothermal alteration system that the ore-forming materials were deep derived from and the ore-forming fluids were dominated by magmatic waters with addition of some atmospheric water in the later phase of mineralization. Gold mineralization took place in an environment of medium to high temperatures and medium pressures. Ore-forming fluids were the K^＋-Na^＋-Ca^2＋-Cl^--SO4^2- type and characterized by medium salinity or a slightly higher, weak alkaline and weak reductive. Au in the ore-forming fluids was transported as complexes of [Au （HS）2]^-, [AuCl2]^-, [Au（CO2）]^- and [Au（HCO3）2]^-. Along with the decline of temperatures and pressures, the ore-forming fluids varied from acidic to weak acidic and then to weak alkaline, which resulted in the dissociation of the complex and finally the precipitation of the gold.     

Radioactive Genesis of Hydrogen Gas under Geological Conditions: an Experimental Study

The coexistence of hydrogen-containing materials and radioactive substances in source rocks is universal. Few documents have researched whether the latter can radiate the former to generate hydrogen gas (H2) as well as the factors controlling this process. This work conducted a series of radiation experiments to address this issue. Samples were placed in sealed Pyrex glass containers and subject to cobalt (60Co) γ irradiation and components and contents of resultant gases were analyzed using gas-chromatography. The results show that all the samples released variable amounts of H2 after irradiation and that the yield (H2) of decane is lower than that of 3-tetradecylthiophene but higher than that of distilled water, which implies that a weaker H-X bond energy (X indicates O, C or other element) in homogeneous materials corresponds with increased yield (H2). The yields (H2) of samples decreased with the decreasing solutions concentrations in sequence from mixed salts solution, KCl solution, Yellow Sea water, oil field water, gypsum solution to distilled water. The experimental results also show that the yield (H2) of distilled water with montmorillonite is higher than that of distilled water with kaolinite, because due to the larger specific surface area, ion exchange capacity and more effective energy transfer effect of montmorillonite. Meanwhile, the irradiation of oxygen- and carbon-containing materials also releases O2 and CH4. The production of H2 via the irradiation of hydrogen-containing materials makes the involvement of exogenous H2 into hydrocarbon generation possible, which can enhance the hydrocarbon volume and optimize crude oil.     

Morphology, Chemistry and U-Pb Geochronology of Zircon Grains In Quartz Monzodiorite from the Sunzhuang Area, Fanshi County, Shanxi Province

The morphology, REE geochemistry and U-Pb geochronology of zircons from quartz monzodiorite in the Sunzhuang area, Fanshi County, Shanxi Province are presented in this study. The zircon crystals can be classified into four main types as: AB, L, S and P, and 24 subtypes such as AB4, AB5, L5, and S3. The maximum crystallization temperature of zircon was estimated as 850°C, with the minimum of 550°C. The peak temperatures of the zircon crystallization range from 650°C to 700°C. The abundances of Th and U in the zircon grains show large variation with the Th/U values 0.4. The Th and U values also show a positive correlation in most zircons. The REE abundance of zircon in the quartz monzodiorite ranges from 280.4 ppm to 2143 ppm with an average of 856.4 ppm. The chondrite normalized zircon REE patterns show two types, one is characterized by HREE enrichment and LREE depletion with positive Ce-anomaly and negative Eu-anomaly whereas the other is HREE enriched and LREE depleted with negative Eu-anomaly but without positive Ce-anomaly, and relatively flat patterns. The LA-ICP-MS U-Pb geochronology on the zircons yields a mean age of 133±0.87 Ma. Our data on zircon morphology, composition and U-Pb geochronology reveal that the parent magma of the quartz monzodiorite which was emplaced during late Yanshanian had a mixed crust-mantle source, with crustal components dominating. The magma is inferred to have been water rich and alkaline with initial high oxygen fugacity. Post-magmatic hydrothermal activity occurred under relatively reducing conditions which was conductive for gold precipitation in the Yixingzhai gold deposit.     

Organic Carbon Isotopic Evolution during the Ediacaran-Cambrian Transition Interval in Eastern Guizhou, South China： Paleoenvironmental and Stratigraphic Implications

Secular variations of carbon isotopic composition of organic carbon can be used in the study of global environmental variation, the carbon cycle, stratigraphic delimitation, and biological evolution, etc. Organic carbon isotopic analysis of the Nangao and Zhalagou sections in eastern Guizhou reveals a negative excursion near the Precambrian-Cambrian boundary that correlates with a distinct carbonate carbon isotopic negative excursion at this boundary globally. Our results also demonstrate that several alternating positive and negative shifts occur in the Meishucunian, and an obvious negative anomaly appears at the boundary between the Meishucunian and Qiongzhusian. The isotope values are stable in the middle and lower parts but became more positive in the upper part of the Qiongzhusian. Evolution of organic carbon isotopes from the two sections in the deepwater facies can be well correlated with that of the carbonate carbon isotopes from the section in the shallow water facies. Integrated with other stratigraphic tools, we can precisely establish a lower Cambrian stratigraphic framework from shallow shelf to deep basin of the Yangtze Platform.     

Experimental Study on the Leaching of Gold from Greenstone

Experiments were conducted on the leaching of gold from greenstone by chloride solution under the temperature of 200—550℃ and the pressure of 60 MPa. During part of the experiments, the oxygen fugacity was controlled. The results show that the leaching rate of gold is related to temperature, composition of the solution, pH and oxygen fugacity. In the experiment with oxidative acidic solution, the leaching rate was up to 50％ or more. It is known that the leaching of gold is restricted by the reaction in which the gold is dissolved from the rock to form gold chloride complex. Therefore, the authors hold that the acidic chloride solution derived from granite magma has caused the remobilization-migration of gold from greenstone and its enrichment into ore.