首页 > 最新文献

Ore Geology Reviews最新文献

英文 中文
Geology and genesis of gold deposits in the daduhe belt: A Case study of the Lianhua gold deposit on the Western margin of the Yangtze Craton, China
IF 3.2 2区 地球科学 Q1 GEOLOGY Pub Date : 2025-02-15 DOI: 10.1016/j.oregeorev.2025.106500
Hongbin Li, Guochen Dong, Zhuolin Xie, Shuai Wang, Yuting Fan
The Daduhe gold belt (DGB) is an essential gold mineralization belts discovered in southwestern China. However, there are still some controversies on the material source, fluid origin and properties. The Lianhua gold deposit, as one of the typical gold deposits in the DGB, is suitable to understand the mineralization. Based on field investigation, and analysis on mineralogy, fluid inclusions, and S-H-O isotope geochemistry, a possible metallogenic model is proposed. According to field observations, the Lianhua deposit has experienced at least two phases of hydrothermal activity, namely, the ore-forming and post-ore periods. Three types of fluid inclusions are identified: 1) VCO2–LH2O (C1 type), 2) VCO2±CH4–LH2O (C2 type), and 3) VH2O–LH2O (W type). The inclusions in ore-forming periods are mainly C1 and C2 type, while the post-ore period is W type predominately. Microthermometric analyses show that ore-forming quartz veins formed in a low to medium temperature (201.6℃–315.2℃), low to medium salinity (3.05–13.20 wt% NaCl eqv.) H2O–NaCl–CO2 ± CH4 system. The H-O isotope of ore-forming quartz shows, the δ18OV-SMOW ranged from 7.29 ‰–10.81 ‰, whereas the δDV-SMOW ranged from − 63.5 ‰–−68.3 ‰, implying that the ore-forming fluids are formed by a mixture of metamorphic fluids and meteoric water. Fluid immiscibility caused by the separation of CO2 ± CH4–H2O system and H2O–NaCl system may be the main mechanism of gold precipitation. The δ34S values of pyrite ranged from − 3.12 ‰–5.92 ‰, indicating that the Kangding complex provided ore-forming materials.
The post-ore tourmaline quartz veins formed in a medium to high temperature (286.6℃–460.1℃), medium to high salinity (9.98–20.26 wt% NaCl eqv.) H2O–NaCl system. The δ18OV-SMOW is 9.16 ‰, whereas the δDV-SMOW is − 85.5 ‰, implying that the post-ore fluids are predominantly primary magmatic water or at least vast magmatic water injection. Tourmaline, as a characteristic mineral of post-ore hydrothermal event, is formed by crustal magmatic fluids reacted with the Kangding complex. However, the post-ore magmatic-hydrothermal fluids did not contribute to the enrichment of gold in the Lianhua deposit.
{"title":"Geology and genesis of gold deposits in the daduhe belt: A Case study of the Lianhua gold deposit on the Western margin of the Yangtze Craton, China","authors":"Hongbin Li,&nbsp;Guochen Dong,&nbsp;Zhuolin Xie,&nbsp;Shuai Wang,&nbsp;Yuting Fan","doi":"10.1016/j.oregeorev.2025.106500","DOIUrl":"10.1016/j.oregeorev.2025.106500","url":null,"abstract":"<div><div>The Daduhe gold belt (DGB) is an essential gold mineralization belts discovered in southwestern China. However, there are still some controversies on the material source, fluid origin and properties. The Lianhua gold deposit, as one of the typical gold deposits in the DGB, is suitable to understand the mineralization. Based on field investigation, and analysis on mineralogy, fluid inclusions, and S-H-O isotope geochemistry, a possible metallogenic model is proposed. According to field observations, the Lianhua deposit has experienced at least two phases of hydrothermal activity, namely, the ore-forming and post-ore periods. Three types of fluid inclusions are identified: 1) V<sub>CO2</sub>–L<sub>H2O</sub> (C1 type), 2) V<sub>CO2±CH4</sub>–L<sub>H2O</sub> (C2 type), and 3) V<sub>H2O</sub>–L<sub>H2O</sub> (W type). The inclusions in ore-forming periods are mainly C1 and C2 type, while the post-ore period is W type predominately. Microthermometric analyses show that ore-forming quartz veins formed in a low to medium temperature (201.6℃–315.2℃), low to medium salinity (3.05–13.20 wt% NaCl eqv.) H<sub>2</sub>O–NaCl–CO<sub>2</sub> ± CH<sub>4</sub> system. The H-O isotope of ore-forming quartz shows, the δ<sup>18</sup>O<sub>V-SMOW</sub> ranged from 7.29 ‰–10.81 ‰, whereas the δD<sub>V-SMOW</sub> ranged from − 63.5 ‰–−68.3 ‰, implying that the ore-forming fluids are formed by a mixture of metamorphic fluids and meteoric water. Fluid immiscibility caused by the separation of CO<sub>2</sub> ± CH<sub>4</sub>–H<sub>2</sub>O system and H<sub>2</sub>O–NaCl system may be the main mechanism of gold precipitation. The δ<sup>34</sup>S values of pyrite ranged from − 3.12 ‰–5.92 ‰, indicating that the Kangding complex provided ore-forming materials.</div><div>The post-ore tourmaline quartz veins formed in a medium to high temperature (286.6℃–460.1℃), medium to high salinity (9.98–20.26 wt% NaCl eqv.) H<sub>2</sub>O–NaCl system. The δ<sup>18</sup>O<sub>V-SMOW</sub> is 9.16 ‰, whereas the δD<sub>V-SMOW</sub> is − 85.5 ‰, implying that the post-ore fluids are predominantly primary magmatic water or at least vast magmatic water injection. Tourmaline, as a characteristic mineral of post-ore hydrothermal event, is formed by crustal magmatic fluids reacted with the Kangding complex. However, the post-ore magmatic-hydrothermal fluids did not contribute to the enrichment of gold in the Lianhua deposit.</div></div>","PeriodicalId":19644,"journal":{"name":"Ore Geology Reviews","volume":"178 ","pages":"Article 106500"},"PeriodicalIF":3.2,"publicationDate":"2025-02-15","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143445347","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":2,"RegionCategory":"地球科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Bonanza-type epithermal Ag-Au mineralisation in Nová Baňa (Western Carpathians, Slovakia)
IF 3.2 2区 地球科学 Q1 GEOLOGY Pub Date : 2025-02-15 DOI: 10.1016/j.oregeorev.2025.106493
Jozef Vlasáč , Tomáš Mikuš , Juraj Majzlan , Martin Števko , Peter Tuček
The Miocene bonanza-type epithermal mineralisation Šibeničný vrch is located in the western part of the historic Nová Baňa deposit on the western slope of the Štiavnica stratovolcano. In the near-surface primary samples, bonanza accumulations contain up to 1700 ppm Ag and 283 ppm Au, while the Cu content does not exceed 59 ppm. This unusual geochemical signature, where Au exceeds Cu, Pb, or Zn, led to formation of unique mineral association in the studied samples. In this work, we focus on this mineral assemblage and its formation. The bonanza ores are banded, with rhythmically alternating chalcedony, quartz with enclosed adularia, and irregular accumulations of precious-metal minerals. The mineral assemblage hosted in the near-surface samples comprises pyrite, rozhdestvenskayaite-(Zn), zvěstovite-(Zn), zvěstovite-(Fe), argentopolybasite, argentopearceite, auropolybasite, auropearceite, Au-Ag alloys, stephanite, selenostephanite, pyrargyrite, proustite, naumannite, uytenbogaardtite, iodargyrite, and bromargyrite. These minerals document high concentration of Au, Ag, Sb, As, Se, and S in the fluid, simultaneously with lack of Cu, Pb, and Zn. Some of these sulfides incorporated Au in their structure, even though under usual geochemical conditions, they would not do so. The deeper parts of the same vein (163–166 m below the current surface) are characterised by lower Au and Ag contents (<84 ppm Ag, <6.95 ppm Au) and the mineral assemblage of chalcopyrite, galena, sphalerite, Au-Ag alloys, polybasite, and pearceite. Ore-bearing colloform bands of chalcedony consist of various textures, predominantly mosaic, acicular/pseudoacicular, flamboyant, or moss textures. We assume that the genesis of these chalcedony forms is related to the fluid boiling. Crustiform quartz in the deeper parts of the vein is most likely related to fluid mixing. Two possible metal transport mechanisms were cooperating in the ore-forming processes, either in bisulfide complexes or in the form of colloids (nanoparticles). Precious-metal enrichment and gangue in studied bonanza-type mineralisation links to the combination of vigorous boiling of the fluid and fluid mixing with meteoric water in the sub-surface environment. Hydrothermal breccias range from small enclaves within veinlets in the deeper parts of the studied mineralisation, but extend vertically to form pipelike body in the uppermost parts. The widespread hydrothermal breccias show that boiling was more intensive in the near-surface zone. In contrast, fluid mixing likely triggered metal precipitation in the deeper parts of the deposit.
{"title":"Bonanza-type epithermal Ag-Au mineralisation in Nová Baňa (Western Carpathians, Slovakia)","authors":"Jozef Vlasáč ,&nbsp;Tomáš Mikuš ,&nbsp;Juraj Majzlan ,&nbsp;Martin Števko ,&nbsp;Peter Tuček","doi":"10.1016/j.oregeorev.2025.106493","DOIUrl":"10.1016/j.oregeorev.2025.106493","url":null,"abstract":"<div><div>The Miocene bonanza-type epithermal mineralisation Šibeničný vrch is located in the western part of the historic Nová Baňa deposit on the western slope of the Štiavnica stratovolcano. In the near-surface primary samples, bonanza accumulations contain up to 1700 ppm Ag and 283 ppm Au, while the Cu content does not exceed 59 ppm. This unusual geochemical signature, where Au exceeds Cu, Pb, or Zn, led to formation of unique mineral association in the studied samples. In this work, we focus on this mineral assemblage and its formation. The bonanza ores are banded, with rhythmically alternating chalcedony, quartz with enclosed adularia, and irregular accumulations of precious-metal minerals. The mineral assemblage hosted in the near-surface samples comprises pyrite, rozhdestvenskayaite-(Zn), zvěstovite-(Zn), zvěstovite-(Fe), argentopolybasite, argentopearceite, auropolybasite, auropearceite, Au-Ag alloys, stephanite, selenostephanite, pyrargyrite, proustite, naumannite, uytenbogaardtite, iodargyrite, and bromargyrite. These minerals document high concentration of Au, Ag, Sb, As, Se, and S in the fluid, simultaneously with lack of Cu, Pb, and Zn. Some of these sulfides incorporated Au in their structure, even though under usual geochemical conditions, they would not do so. The deeper parts of the same vein (163–166 m below the current surface) are characterised by lower Au and Ag contents (&lt;84 ppm Ag, &lt;6.95 ppm Au) and the mineral assemblage of chalcopyrite, galena, sphalerite, Au-Ag alloys, polybasite, and pearceite. Ore-bearing colloform bands of chalcedony consist of various textures, predominantly mosaic, acicular/pseudoacicular, flamboyant, or moss textures. We assume that the genesis of these chalcedony forms is related to the fluid boiling. Crustiform quartz in the deeper parts of the vein is most likely related to fluid mixing. Two possible metal transport mechanisms were cooperating in the ore-forming processes, either in bisulfide complexes or in the form of colloids (nanoparticles). Precious-metal enrichment and gangue in studied bonanza-type mineralisation links to the combination of vigorous boiling of the fluid and fluid mixing with meteoric water in the sub-surface environment. Hydrothermal breccias range from small enclaves within veinlets in the deeper parts of the studied mineralisation, but extend vertically to form pipelike body in the uppermost parts. The widespread hydrothermal breccias show that boiling was more intensive in the near-surface zone. In contrast, fluid mixing likely triggered metal precipitation in the deeper parts of the deposit.</div></div>","PeriodicalId":19644,"journal":{"name":"Ore Geology Reviews","volume":"178 ","pages":"Article 106493"},"PeriodicalIF":3.2,"publicationDate":"2025-02-15","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143445350","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":2,"RegionCategory":"地球科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Petrological and geochemical studies of the Xiamaidi mafic–ultramafic intrusion in the Baoshan block, with implications for Ni exploration
IF 3.2 2区 地球科学 Q1 GEOLOGY Pub Date : 2025-02-15 DOI: 10.1016/j.oregeorev.2025.106490
Jinyu Liu , Shengchao Xue , Yuguang Zhang , Qingfei Wang , Luyang Wang , Chusi Li , Jun Deng
Many major magmatic Ni-Cu-Co sulfide deposits worldwide occur in the magma plumbing systems of continental flood basalt. The Xiamaidi mafic–ultramafic intrusion (∼291 Ma) is associated with the Baoshan Late Paleozoic continental flood basalts in southwestern China and hosts important information about the role of magma differentiation in sulfide mineralization in the magma plumbing systems. We address this question by comparing the petrological and geochemical features between the Xiamaidi intrusion and the Daxueshan magmatic Ni-Cu-Co sulfide deposit. The Daxueshan deposit is hosted by a mafic–ultramafic intrusion (∼301 Ma) that is also associated with the Baoshan basalts. The olivine Fo contents of in both intrusions overlap (72–83 mol%), but the Xiamaidi intrusion tends to have slightly lower olivine Fo contents. The olivine of the Xiamaidi intrusive rocks is relatively depleted in Ni (∼600–1300 ppm) and shows no correlation with Fo contents, indicating that multiple pulses of parental magma were involved in the formation of this intrusion. The contents of platinum group elements (PGE) in the Xiamaidi intrusive rocks are about one order of magnitude lower than in the reported Baoshan basalts. The Cu/Pd ratios of the Xiamaidi intrusive rocks and the Daxueshan deposit are similar and are all significantly higher than the ratios of the Baoshan basalts (0.77 × 104 to 4.0 × 104), indicating that the parental magmas for both intrusions had experienced early sulfide segregation at greater depths. Compared to the Baoshan basalts, the Xiamaidi and Daxueshan intrusive rocks have larger negative Nb-Ta anomalies, lower εNd(t) values (–5.7 to –7.9) and higher (87Sr/86Sr)i ratios (0.7111 to 0.7135) than the average compositions of the basalts [εNd(t) = –1.9; (87Sr/86Sr)i = 0.7073]. The differences can be explained by different mantle sources plus variable crustal contamination, with the parental magmas for the intrusive rocks derived predominantly from a subcontinental lithospheric mantle whereas the flood basalts derived mainly from the underlying mantle plume. The estimated amounts of crustal contamination in the parental magmas for the Xiamaidi and Daxueshan intrusions vary from 15 to 30 wt%. The whole-rock Sr-Nd isotopic and trace elemental data support the view that sulfide saturation in the parental magmas was mainly induced by crustal contamination. The most important implications for Ni exploration from this study are (1) at an intrusion scale, future exploration should focus on the feeders of the Xiamaidi and Daxueshan intrusive systems, and (2) at a regional scale, the ultramafic intrusions containing olivine with higher Fo contents than that in the Xiamaidi ultramafic rocks are the most favorable exploration targets in the Baoshan block.
世界上许多主要的岩浆型镍铜钴硫化物矿床都出现在大陆洪积玄武岩的岩浆管道系统中。下马垅黑云母-超黑云母侵入体(∼291 Ma)与中国西南部的保山晚古生代大陆洪积玄武岩有关,蕴藏着岩浆分异在岩浆垂管系统中硫化物成矿作用的重要信息。我们通过比较夏麦地侵入体和大雪山岩浆镍铜钴硫化物矿床的岩石学和地球化学特征来解决这个问题。大雪山矿床的岩浆岩-超基性侵入体(∼301 Ma)也与宝山玄武岩有关。两个侵入体的橄榄石Fo含量相重叠(72-83 mol%),但下马垅侵入体的橄榄石Fo含量略低。霞麦地侵入岩橄榄石的镍含量相对较低(∼600-1300 ppm),且与萤石含量无相关性,表明该侵入体的形成涉及多个母岩浆脉冲。下马垅侵入岩中的铂族元素含量比已报道的宝山玄武岩中的铂族元素含量低约一个数量级。下马垅侵入岩和大雪山矿床的铜/钯比值相近,均明显高于宝山玄武岩(0.77×104~4.0×104),表明这两个侵入体的母岩在更深的地方经历了早期硫化物偏析。与宝山玄武岩相比,夏麦地和大雪山侵入岩的Nb-Ta负异常较大,εNd(t)值(-5.7至-7.9)较低,(87Sr/86Sr)i比(0.7111至0.7135)高于玄武岩的平均成分[εNd(t)=-1.9;(87Sr/86Sr)i=0.7073]。侵入岩的母岩主要来自次大陆岩石圈地幔,而洪积玄武岩则主要来自下伏地幔羽流。据估计,夏麦地和大雪山侵入岩的母岩浆中地壳污染的含量从15%到30%不等。全岩Sr-Nd同位素和痕量元素数据支持母岩浆中硫化物饱和主要由地壳污染引起的观点。本研究对镍矿勘探最重要的启示是:(1)在侵入体尺度上,未来勘探的重点应放在下马垅和大雪山侵入系统的赋存体上;(2)在区域尺度上,含萤石含量高于下马垅超基性岩的橄榄岩的超基性侵入体是宝山区块最有利的勘探目标。
{"title":"Petrological and geochemical studies of the Xiamaidi mafic–ultramafic intrusion in the Baoshan block, with implications for Ni exploration","authors":"Jinyu Liu ,&nbsp;Shengchao Xue ,&nbsp;Yuguang Zhang ,&nbsp;Qingfei Wang ,&nbsp;Luyang Wang ,&nbsp;Chusi Li ,&nbsp;Jun Deng","doi":"10.1016/j.oregeorev.2025.106490","DOIUrl":"10.1016/j.oregeorev.2025.106490","url":null,"abstract":"<div><div>Many major magmatic Ni-Cu-Co sulfide deposits worldwide occur in the magma plumbing systems of continental flood basalt. The Xiamaidi mafic–ultramafic intrusion (∼291 Ma) is associated with the Baoshan Late Paleozoic continental flood basalts in southwestern China and hosts important information about the role of magma differentiation in sulfide mineralization in the magma plumbing systems. We address this question by comparing the petrological and geochemical features between the Xiamaidi intrusion and the Daxueshan magmatic Ni-Cu-Co sulfide deposit. The Daxueshan deposit is hosted by a mafic–ultramafic intrusion (∼301 Ma) that is also associated with the Baoshan basalts. The olivine Fo contents of in both intrusions overlap (72–83 mol%), but the Xiamaidi intrusion tends to have slightly lower olivine Fo contents. The olivine of the Xiamaidi intrusive rocks is relatively depleted in Ni (∼600–1300 ppm) and shows no correlation with Fo contents, indicating that multiple pulses of parental magma were involved in the formation of this intrusion. The contents of platinum group elements (PGE) in the Xiamaidi intrusive rocks are about one order of magnitude lower than in the reported Baoshan basalts. The Cu/Pd ratios of the Xiamaidi intrusive rocks and the Daxueshan deposit are similar and are all significantly higher than the ratios of the Baoshan basalts (0.77 × 10<sup>4</sup> to 4.0 × 10<sup>4</sup>), indicating that the parental magmas for both intrusions had experienced early sulfide segregation at greater depths. Compared to the Baoshan basalts, the Xiamaidi and Daxueshan intrusive rocks have larger negative Nb-Ta anomalies, lower ε<sub>Nd</sub>(t) values (–5.7 to –7.9) and higher (<sup>87</sup>Sr/<sup>86</sup>Sr)<sub>i</sub> ratios (0.7111 to 0.7135) than the average compositions of the basalts [ε<sub>Nd</sub>(t) = –1.9; (<sup>87</sup>Sr/<sup>86</sup>Sr)<sub>i</sub> = 0.7073]. The differences can be explained by different mantle sources plus variable crustal contamination, with the parental magmas for the intrusive rocks derived predominantly from a subcontinental lithospheric mantle whereas the flood basalts derived mainly from the underlying mantle plume. The estimated amounts of crustal contamination in the parental magmas for the Xiamaidi and Daxueshan intrusions vary from 15 to 30 wt%. The whole-rock Sr-Nd isotopic and trace elemental data support the view that sulfide saturation in the parental magmas was mainly induced by crustal contamination. The most important implications for Ni exploration from this study are (1) at an intrusion scale, future exploration should focus on the feeders of the Xiamaidi and Daxueshan intrusive systems, and (2) at a regional scale, the ultramafic intrusions containing olivine with higher Fo contents than that in the Xiamaidi ultramafic rocks are the most favorable exploration targets in the Baoshan block.</div></div>","PeriodicalId":19644,"journal":{"name":"Ore Geology Reviews","volume":"178 ","pages":"Article 106490"},"PeriodicalIF":3.2,"publicationDate":"2025-02-15","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143445346","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":2,"RegionCategory":"地球科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Metallogeny of the Jinming gold deposit in northeast Hunan, Jiangnan Orogen: Constraints from in situ sericite Rb-Sr dating, pyrite trace elements and S isotope geochemistry
IF 3.2 2区 地球科学 Q1 GEOLOGY Pub Date : 2025-02-15 DOI: 10.1016/j.oregeorev.2025.106499
Zhaohua Chen , Yongjun Shao , Qingquan Liu , Xiong Zhang , Yuce Zhang , Hongtao Zhao , Jie Chen , Lijun Hu
The newly discovered Jinming gold deposit in northeastern Hunan province (Eastern China) is tectonically located in the Jiangnan Orogen. The fault-controlled auriferous quartz ore veins are primarily developed in the low-grade metamorphosed Neoproterozoic Lengjiaxi Group. The alteration/mineralization comprises stage I quartz-pyrite mineralization, stage II quartz-native gold-polymetallic sulfide mineralization, and stage Ⅲ quartz-carbonate veining. Our in situ sericite Rb-Sr dating on stage II ore yielded an Early Devonian age of 412.4 ± 8.4 Ma (MSWD = 1.1). Five types of pyrite were identified, i.e., Py1 (Py1a and Py1b) in stage Ⅰ, and Py2 (Py2a, Py2b, and Py2c) in stage Ⅱ. Py1 has relatively low trace element contents and narrow δ34S range (Py1a: −5.53 to −4.82 ‰, Py1b: −5.29 to −4.72 ‰), whereas Py2 is Au-As-Co-Ni rich with a broader δ34S range (Py2a: −6.00 to −4.94 ‰, Py2b: −13.80 to −7.99 ‰, Py2c: –23.45 to −18.70 ‰). The distinct trace element and sulfur isotope features in Py1 and Py2 imply major physicochemical changes in the ore-forming fluids from stage I to II. At Jinming, gold occurs as native gold and refractory gold (Au+) in pyrite and arsenopyrite from stage II, and the invisible gold is primarily found as solid solution gold (Au+) within the lattice structure of pyrite. A marked positive correlation between the concentrations of Au and arsenic (As) in pyrite suggests a strong relationship between Au enrichment and As content. The pyrite’s element and sulfur isotope features imply a deep metamorphosed strata source for the ore material at Jinming. Geological and geochemical evidence suggests that the Jinming gold deposit is best classified as an orogenic type, associated with the Caledonian intracontinental orogeny.
新发现的金明金矿床位于湖南省东北部(中国东部)的江南造山带。受断层控制的含金石英矿脉主要发育于低品位变质的新新生代冷家溪组。蚀变/矿化包括Ⅰ期石英-黄铁矿化、Ⅱ期石英-原生金-多金属硫化物矿化和Ⅲ期石英-碳酸盐脉。我们对Ⅱ期矿石进行了绢云母Rb-Sr原位定年,得出的早泥盆世年龄为412.4 ± 8.4 Ma(MSWD = 1.1)。鉴定出五种类型的黄铁矿,即Ⅰ期的Py1(Py1a和Py1b)和Ⅱ期的Py2(Py2a、Py2b和Py2c)。Py1的微量元素含量相对较低,δ34S范围较窄(Py1a:-5.53~-4.82‰,Py1b:-5.29~-4.72‰),而Py2富含Au-As-Co-Ni,δ34S范围较宽(Py2a:-6.00~-4.94‰,Py2b:-13.80~-7.99‰,Py2c:-23.45~-18.70‰)。Py1和Py2的微量元素和硫同位素特征明显,这意味着成矿流体从第一阶段到第二阶段发生了重大的物理化学变化。在金明,从第二阶段开始,金以原生金和难熔金(Au+)的形式出现在黄铁矿和砷黄铁矿中,而隐形金主要以固溶金(Au+)的形式出现在黄铁矿的晶格结构中。黄铁矿中金(Au)和砷(As)的浓度呈明显的正相关,表明金富集与砷含量之间存在密切关系。黄铁矿的元素和硫同位素特征意味着金明矿石材料来源于深变质地层。地质和地球化学证据表明,金明金矿床最好归类为造山类型,与加里东大陆内造山运动有关。
{"title":"Metallogeny of the Jinming gold deposit in northeast Hunan, Jiangnan Orogen: Constraints from in situ sericite Rb-Sr dating, pyrite trace elements and S isotope geochemistry","authors":"Zhaohua Chen ,&nbsp;Yongjun Shao ,&nbsp;Qingquan Liu ,&nbsp;Xiong Zhang ,&nbsp;Yuce Zhang ,&nbsp;Hongtao Zhao ,&nbsp;Jie Chen ,&nbsp;Lijun Hu","doi":"10.1016/j.oregeorev.2025.106499","DOIUrl":"10.1016/j.oregeorev.2025.106499","url":null,"abstract":"<div><div>The newly discovered Jinming gold deposit in northeastern Hunan province (Eastern China) is tectonically located in the Jiangnan Orogen. The fault-controlled auriferous quartz ore veins are primarily developed in the low-grade metamorphosed Neoproterozoic Lengjiaxi Group. The alteration/mineralization comprises stage I quartz-pyrite mineralization, stage II quartz-native gold-polymetallic sulfide mineralization, and stage Ⅲ quartz-carbonate veining. Our in situ sericite Rb-Sr dating on stage II ore yielded an Early Devonian age of 412.4 ± 8.4 Ma (MSWD = 1.1). Five types of pyrite were identified, i.e., Py1 (Py1a and Py1b) in stage Ⅰ, and Py2 (Py2a, Py2b, and Py2c) in stage Ⅱ. Py1 has relatively low trace element contents and narrow δ<sup>34</sup>S range (Py1a: −5.53 to −4.82 ‰, Py1b: −5.29 to −4.72 ‰), whereas Py2 is Au-As-Co-Ni rich with a broader δ<sup>34</sup>S range (Py2a: −6.00 to −4.94 ‰, Py2b: −13.80 to −7.99 ‰, Py2c: –23.45 to −18.70 ‰). The distinct trace element and sulfur isotope features in Py1 and Py2 imply major physicochemical changes in the ore-forming fluids from stage I to II. At Jinming, gold occurs as native gold and refractory gold (Au<sup>+</sup>) in pyrite and arsenopyrite from stage II, and the invisible gold is primarily found as solid solution gold (Au<sup>+</sup>) within the lattice structure of pyrite. A marked positive correlation between the concentrations of Au and arsenic (As) in pyrite suggests a strong relationship between Au enrichment and As content. The pyrite’s element and sulfur isotope features imply a deep metamorphosed strata source for the ore material at Jinming. Geological and geochemical evidence suggests that the Jinming gold deposit is best classified as an orogenic type, associated with the Caledonian intracontinental orogeny.</div></div>","PeriodicalId":19644,"journal":{"name":"Ore Geology Reviews","volume":"178 ","pages":"Article 106499"},"PeriodicalIF":3.2,"publicationDate":"2025-02-15","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143445349","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":2,"RegionCategory":"地球科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Mineral prospectivity mapping of orogenic gold mineralization in the Malartic-Val-d’Or Transect area, Metal Earth project, Canada
IF 3.2 2区 地球科学 Q1 GEOLOGY Pub Date : 2025-02-13 DOI: 10.1016/j.oregeorev.2025.106498
Ahmad Reza Mokhtari, Pouran Behnia, Bruno Lafrance, Mostafa Naghizadeh, Jack M. Simmons, Jeff R. Harris
Mineral Prospectivity Mapping has been applied to define exploration targets for orogenic gold mineralization in the world-class Malartic-Val-d’Or area (Quebec) of the Abitibi greenstone belt, a region that contributes significantly to Canada’s annual gold production. This research utilizes lithological, geophysical, and structural data from the Malartic transect, collected as part of the Metal Earth project, to investigate factors controlling gold distribution in the region. Stepwise logistic regression and random forest algorithms were employed to map mineral prospectivity for gold potential. The overall accuracy indicates that the random forest method has outperformed logistic regression, although the latter produced an acceptable model. This conclusion is supported by the classification accuracy validated using an independent Au occurrence database and the performance metrics generated by the random forest and logistic regression models. Crustal density, shear zones, and faults are strong predictors for distinguishing mineralized and non-mineralized locations, as identified by both Random Forest and Logistic Regression models. In the Malartic-Val-d’Or region, subvertical conductive anomalies revealed by magnetotelluric data align closely with major shear zones and crustal-scale structures, such as the Cadillac-Larder Lake deformation zone, which hosts significant gold deposits. These anomalies suggest a paleo-hydrothermal footprint of mineralizing fluids and highlight their critical role in the formation of orogenic gold deposits, a pattern also observed in other mining camps across the Superior craton. These results and associated mineral prospectivity maps are integral for greenfields exploration in the Malartic region and may offer valuable insights for mineral exploration in other greenstone belts of the Superior craton.
{"title":"Mineral prospectivity mapping of orogenic gold mineralization in the Malartic-Val-d’Or Transect area, Metal Earth project, Canada","authors":"Ahmad Reza Mokhtari,&nbsp;Pouran Behnia,&nbsp;Bruno Lafrance,&nbsp;Mostafa Naghizadeh,&nbsp;Jack M. Simmons,&nbsp;Jeff R. Harris","doi":"10.1016/j.oregeorev.2025.106498","DOIUrl":"10.1016/j.oregeorev.2025.106498","url":null,"abstract":"<div><div>Mineral Prospectivity Mapping has been applied to define exploration targets for orogenic gold mineralization in the world-class Malartic-Val-d’Or area (Quebec) of the Abitibi greenstone belt, a region that contributes significantly to Canada’s annual gold production. This research utilizes lithological, geophysical, and structural data from the Malartic transect, collected as part of the Metal Earth project, to investigate factors controlling gold distribution in the region. Stepwise logistic regression and random forest algorithms were employed to map mineral prospectivity for gold potential. The overall accuracy indicates that the random forest method has outperformed logistic regression, although the latter produced an acceptable model. This conclusion is supported by the classification accuracy validated using an independent Au occurrence database and the performance metrics generated by the random forest and logistic regression models. Crustal density, shear zones, and faults are strong predictors for distinguishing mineralized and non-mineralized locations, as identified by both Random Forest and Logistic Regression models. In the Malartic-Val-d’Or region, subvertical conductive anomalies revealed by magnetotelluric data align closely with major shear zones and crustal-scale structures, such as the Cadillac-Larder Lake deformation zone, which hosts significant gold deposits. These anomalies suggest a paleo-hydrothermal footprint of mineralizing fluids and highlight their critical role in the formation of orogenic gold deposits, a pattern also observed in other mining camps across the Superior craton. These results and associated mineral prospectivity maps are integral for greenfields exploration in the Malartic region and may offer valuable insights for mineral exploration in other greenstone belts of the Superior craton.</div></div>","PeriodicalId":19644,"journal":{"name":"Ore Geology Reviews","volume":"178 ","pages":"Article 106498"},"PeriodicalIF":3.2,"publicationDate":"2025-02-13","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143428122","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":2,"RegionCategory":"地球科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Assessment of pyrite and arsenopyrite compositions, in situ S isotopes, and bulk Pb isotopes from the Cape Spencer gold deposit, New Brunswick, Canada 加拿大新不伦瑞克斯潘塞角金矿床黄铁矿和砷黄铁矿成分、原位 S 同位素和大块铅同位素评估
IF 3.2 2区 地球科学 Q1 GEOLOGY Pub Date : 2025-02-12 DOI: 10.1016/j.oregeorev.2025.106492
Alan Cardenas-Vera , David R. Lentz , Christopher R.M. McFarlane , Kathleen G. Thorne
The Cape Spencer gold deposit is situated proximal to the boundary between two major lithotectonic zones of the Canadian Appalachians, the Caledonia and Meguma terranes, within a fold-thrust belt in southern New Brunswick along the Minas Fault Zone. Gold mineralization occurs in quartz-dominant veins with 2–5 % sulphides hosted by the highly deformed and sheared rocks of the Millican Lake Granite and the Cape Spencer Formation. In this research, in situ S isotope and trace-element concentrations of pyrite in combination with bulk pyrite Pb isotope analyses are presented to better understand the metal sources, fluid channels, and mechanisms of ore deposition. Based on textural characteristics and trace element concentrations, five generations of pyrite from the hydrothermal stage were identified in the ore bodies: Py1a, Py1b, Py2a, Py2b, and Py3. The first pyrite generations, Py1a and Py1b (substage I), contain higher concentrations of Co and Ni than pyrite from substages II and III and have positive δ34S values ranging from +6.8 to +18.7 ‰. Economic concentrations of gold are associated with Py2a and Py2b (substage II), which occur as spongy and porous pyrite; Py2a pyrites contain visible gold along fractures and margins. Py1a to Py2b display an Au-Ag-Pb-Bi-Te association, also supported by the presence of hessite, petzite, sylvanite, and native bismuth in the gold ores. Pyrites from substage II display slightly less positive values of δ34S of +1.0 to +12.3 ‰. The last identified pyrite generation, Py3 (substage III), contains no gold and is characterized by high concentrations of As and Cu compared with pyrites from the previous generations and negative δ34S values of −9.8 to −3.8 ‰. This sequential shift towards more negative values from Py1 to Py2 may be induced by phase separation and wall-rock sulphidation processes, in addition to interaction with rocks of the Lancaster Formation for Py3. The generally low gold contents (<0.3 ppm) in pyrite and visible gold within fractures and along pyrite grain margins suggest post-depositional dissolution of pyrite. The influx of ore fluids, consistent with cyclic decompression, induced the removal of iron from Fe-bearing minerals, mainly specular hematite that led to an increase of the Fe in the fluid, destabilizing the Au(HS)2- complexes and promoted the depletion of S and subsequent gold precipitation. The ore-forming fluids were transported along major structures and derived from a mixed source that includes intrusive and metasedimentary rocks from the Avalonia and Meguma terranes, sharing similar characteristics to those values from the Meguma gold deposits, as indicated by both the S and Pb isotope signatures.
{"title":"Assessment of pyrite and arsenopyrite compositions, in situ S isotopes, and bulk Pb isotopes from the Cape Spencer gold deposit, New Brunswick, Canada","authors":"Alan Cardenas-Vera ,&nbsp;David R. Lentz ,&nbsp;Christopher R.M. McFarlane ,&nbsp;Kathleen G. Thorne","doi":"10.1016/j.oregeorev.2025.106492","DOIUrl":"10.1016/j.oregeorev.2025.106492","url":null,"abstract":"<div><div>The Cape Spencer gold deposit is situated proximal to the boundary between two major lithotectonic zones of the Canadian Appalachians, the Caledonia and Meguma terranes, within a fold-thrust belt in southern New Brunswick along the Minas Fault Zone. Gold mineralization occurs in quartz-dominant veins with 2–5 % sulphides hosted by the highly deformed and sheared rocks of the Millican Lake Granite and the Cape Spencer Formation. In this research, <em>in situ</em> S isotope and trace-element concentrations of pyrite in combination with bulk pyrite Pb isotope analyses are presented to better understand the metal sources, fluid channels, and mechanisms of ore deposition. Based on textural characteristics and trace element concentrations, five generations of pyrite from the hydrothermal stage were identified in the ore bodies: Py1a, Py1b, Py2a, Py2b, and Py3. The first pyrite generations, Py1a and Py1b (substage I), contain higher concentrations of Co and Ni than pyrite from substages II and III and have positive δ<sup>34</sup>S values ranging from +6.8 to +18.7 ‰. Economic concentrations of gold are associated with Py2a and Py2b (substage II), which occur as spongy and porous pyrite; Py2a pyrites contain visible gold along fractures and margins. Py1a to Py2b display an Au-Ag-Pb-Bi-Te association, also supported by the presence of hessite, petzite, sylvanite, and native bismuth in the gold ores. Pyrites from substage II display slightly less positive values of δ<sup>34</sup>S of +1.0 to +12.3 ‰. The last identified pyrite generation, Py3 (substage III), contains no gold and is characterized by high concentrations of As and Cu compared with pyrites from the previous generations and negative δ<sup>34</sup>S values of −9.8 to −3.8 ‰. This sequential shift towards more negative values from Py1 to Py2 may be induced by phase separation and wall-rock sulphidation processes, in addition to interaction with rocks of the Lancaster Formation for Py3. The generally low gold contents (&lt;0.3 ppm) in pyrite and visible gold within fractures and along pyrite grain margins suggest post-depositional dissolution of pyrite. The influx of ore fluids, consistent with cyclic decompression, induced the removal of iron from Fe-bearing minerals, mainly specular hematite that led to an increase of the Fe in the fluid, destabilizing the <span><math><msubsup><mrow><mi>A</mi><mi>u</mi><mo>(</mo><mi>H</mi><mi>S</mi><mo>)</mo></mrow><mrow><mn>2</mn></mrow><mo>-</mo></msubsup></math></span> complexes and promoted the depletion of S and subsequent gold precipitation. The ore-forming fluids were transported along major structures and derived from a mixed source that includes intrusive and metasedimentary rocks from the Avalonia and Meguma terranes, sharing similar characteristics to those values from the Meguma gold deposits, as indicated by both the S and Pb isotope signatures.</div></div>","PeriodicalId":19644,"journal":{"name":"Ore Geology Reviews","volume":"178 ","pages":"Article 106492"},"PeriodicalIF":3.2,"publicationDate":"2025-02-12","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143422208","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":2,"RegionCategory":"地球科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Biogenic mineralization controls exceptional REY enrichment in Early Cambrian phosphorites from South China
IF 3.2 2区 地球科学 Q1 GEOLOGY Pub Date : 2025-02-11 DOI: 10.1016/j.oregeorev.2025.106497
Rou Peng , Ruidong Yang , Jiyan Chen , Junbo Gao , Lei Gao , Chuanqian Gao
The Early Cambrian represents a globally significant phosphorus-formation period, particularly noted for producing REY-rich phosphorites in South China. However, substantial differences exist in the REY enrichment levels among these phosphorites. Particularly, the REY contents of the Early Cambrian Meishucun Stage phosphorites from Guizhou and Yunnan exhibit pronounced disparities, with the controlling factors behind these variations remaining a subject of debate. To address this issue, this study conducted comparative analyses of representative REY-bearing phosphorites from Cambrian Meishucun Stage in Bailongtan, Yunnan province, and Zhijin, Guizhou province, China. Advanced analytic techniques, including XRF, ICP-MS, and ICP-OES, were employed to determine major, trace elements and REY concentrations in different phosphorite types. And complementary methodologies including OM, SM, SEM-EDS, and EPMA were utilized to examine the mineralogical and textural features. The results indicated that biofossils preserved in the phosphorites of both regions are small shelly fossils (SSFs), with carbonate fluorapatite as the principal component. Zhijin phosphorites exhibit significantly higher REY enrichment compared with Bailongtan phosphorites, and REY contents positively correlate with the abundance of SSFs. In-situ analyses revealed that REYs are primarily concentrated within SSFs, which were better preserved in oxic and open environments with relatively slow sedimentation rates. The multilayered nested structures of SSFs facilitate the absorption of REYs from seawater and porewater, which corresponding to the biogenic structures of bioapatite observed in modern deep-sea REY-rich sediments. These findings suggested that SSFs play a crucial role in REY enrichment, with Zhijinites potentially serving as the optimal host phase for REY enrichment. Conclusively, biota play an important part in the REY-rich mineralization of phosphorites, offering new insights into the genesis of global sedimentary REY-bearing phosphorites. This understanding also opens new considerations for optimizing REY extraction processes from such phosphorites.
{"title":"Biogenic mineralization controls exceptional REY enrichment in Early Cambrian phosphorites from South China","authors":"Rou Peng ,&nbsp;Ruidong Yang ,&nbsp;Jiyan Chen ,&nbsp;Junbo Gao ,&nbsp;Lei Gao ,&nbsp;Chuanqian Gao","doi":"10.1016/j.oregeorev.2025.106497","DOIUrl":"10.1016/j.oregeorev.2025.106497","url":null,"abstract":"<div><div>The Early Cambrian represents a globally significant phosphorus-formation period, particularly noted for producing REY-rich phosphorites in South China. However, substantial differences exist in the REY enrichment levels among these phosphorites. Particularly, the REY contents of the Early Cambrian Meishucun Stage phosphorites from Guizhou and Yunnan exhibit pronounced disparities, with the controlling factors behind these variations remaining a subject of debate. To address this issue, this study conducted comparative analyses of representative REY-bearing phosphorites from Cambrian Meishucun Stage in Bailongtan, Yunnan province, and Zhijin, Guizhou province, China. Advanced analytic techniques, including XRF, ICP-MS, and ICP-OES, were employed to determine major, trace elements and REY concentrations in different phosphorite types. And complementary methodologies including OM, SM, SEM-EDS, and EPMA were utilized to examine the mineralogical and textural features. The results indicated that biofossils preserved in the phosphorites of both regions are small shelly fossils (SSFs), with carbonate fluorapatite as the principal component. Zhijin phosphorites exhibit significantly higher REY enrichment compared with Bailongtan phosphorites, and REY contents positively correlate with the abundance of SSFs. In-situ analyses revealed that REYs are primarily concentrated within SSFs, which were better preserved in oxic and open environments with relatively slow sedimentation rates. The multilayered nested structures of SSFs facilitate the absorption of REYs from seawater and porewater, which corresponding to the biogenic structures of bioapatite observed in modern deep-sea REY-rich sediments. These findings suggested that SSFs play a crucial role in REY enrichment, with <em>Zhijinites</em> potentially serving as the optimal host phase for REY enrichment. Conclusively, biota play an important part in the REY-rich mineralization of phosphorites, offering new insights into the genesis of global sedimentary REY-bearing phosphorites. This understanding also opens new considerations for optimizing REY extraction processes from such phosphorites.</div></div>","PeriodicalId":19644,"journal":{"name":"Ore Geology Reviews","volume":"178 ","pages":"Article 106497"},"PeriodicalIF":3.2,"publicationDate":"2025-02-11","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143422210","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":2,"RegionCategory":"地球科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
The role of fluid exsolution in the Li enrichment in granitic pegmatites: A case study from the Dahongliutan Li ore field in West Kunlun
IF 3.2 2区 地球科学 Q1 GEOLOGY Pub Date : 2025-02-10 DOI: 10.1016/j.oregeorev.2025.106491
Zhong-Cheng Zeng , Jing-Jing Fan , Zi-Long Wang , Biao Du , Peng Wang , Zeng-Lin Hong
Pegmatite-host Li deposits provide substantial Li resource in the globe. However, the mechanism of Li enrichment in granitic pegmatites remain enigmatic. Here, we report age and whole-rock geochemical data for the garnet-tourmaline-bearing granites (GTGs) and tourmaline-bearing granites (TGs) from the Dahongliutan rare-metal pegmatite ore field located in the Western Kunlun orogen, NW China. The formation of Li-rich pegmatites in this ore field was proposed to have an intimate temporal-spatial association to the two-mica granites (TMGs). Zircon U–Pb dating for the GTGs and TGs yielded ages of 203.2 ± 2.3 and 203.4 ± 2.7 Ma, respectively. These ages are slightly younger than those of the TMGs (ca. 220–208 Ma), but overlapping with or older than those of the Li-rich pegmatites (ca. 214–190 Ma) reported in this area. The GTGs and TGs have middle to upper crust-like Sr–Nd isotope compositions ((87Sr/86Sr)i = 0.7159–0.7227; εNd(t) =   10.7 to  9.67), similar to those of the TMGs and Li-rich pegmatites. The decreasing CaO, MgO, TFe2O3, Sr, Ba and rare earth element contents, and increasing Na2O, K2O contents and Na2O/K2O ratios from the TMGs to GTGs, and to TGs, suggests fractionation of biotite, plagioclase and K-feldspar, monazite, muscovite, and garnet from the TMG magma. These evidence together with the field observations indicate that these granites and pegmatites in the Dahongliutan ore field represent a cogenetic evolutionary sequence. However, the contents of the incompatible element of Li decrease sharply from the TMGs to GTGs and TGs, which is likely resulted from magmatic fluid exsolution. Geochemical modeling for Li show that fluid saturation occurred at the early stage of magma evolution. In the following, the exsoluted fluids accumulation accompany by extraction of large amounts of fluid-soluble elements such as Li and Cs from the residual melts, and their removal and migration away from the granite system, may be pivotal in the generation of the Li-rich pegmatites.
{"title":"The role of fluid exsolution in the Li enrichment in granitic pegmatites: A case study from the Dahongliutan Li ore field in West Kunlun","authors":"Zhong-Cheng Zeng ,&nbsp;Jing-Jing Fan ,&nbsp;Zi-Long Wang ,&nbsp;Biao Du ,&nbsp;Peng Wang ,&nbsp;Zeng-Lin Hong","doi":"10.1016/j.oregeorev.2025.106491","DOIUrl":"10.1016/j.oregeorev.2025.106491","url":null,"abstract":"<div><div>Pegmatite-host Li deposits provide substantial Li resource in the globe. However, the mechanism of Li enrichment in granitic pegmatites remain enigmatic. Here, we report age and whole-rock geochemical data for the garnet-tourmaline-bearing granites (GTGs) and tourmaline-bearing granites (TGs) from the Dahongliutan rare-metal pegmatite ore field located in the Western Kunlun orogen, NW China. The formation of Li-rich pegmatites in this ore field was proposed to have an intimate temporal-spatial association to the two-mica granites (TMGs). Zircon U–Pb dating for the GTGs and TGs yielded ages of 203.2 ± 2.3 and 203.4 ± 2.7 Ma, respectively. These ages are slightly younger than those of the TMGs (ca. 220–208 Ma), but overlapping with or older than those of the Li-rich pegmatites (ca. 214–190 Ma) reported in this area. The GTGs and TGs have middle to upper crust-like Sr–Nd isotope compositions ((<sup>87</sup>Sr/<sup>86</sup>Sr)<sub>i</sub> = 0.7159–0.7227; ε<sub>Nd</sub>(<em>t</em>) =  <strong>−</strong> 10.7 to <strong>−</strong> 9.67), similar to those of the TMGs and Li-rich pegmatites. The decreasing CaO, MgO, TFe<sub>2</sub>O<sub>3</sub>, Sr, Ba and rare earth element contents, and increasing Na<sub>2</sub>O, K<sub>2</sub>O contents and Na<sub>2</sub>O/K<sub>2</sub>O ratios from the TMGs to GTGs, and to TGs, suggests fractionation of biotite, plagioclase and K-feldspar, monazite, muscovite, and garnet from the TMG magma. These evidence together with the field observations indicate that these granites and pegmatites in the Dahongliutan ore field represent a cogenetic evolutionary sequence. However, the contents of the incompatible element of Li decrease sharply from the TMGs to GTGs and TGs, which is likely resulted from magmatic fluid exsolution. Geochemical modeling for Li show that fluid saturation occurred at the early stage of magma evolution. In the following, the exsoluted fluids accumulation accompany by extraction of large amounts of fluid-soluble elements such as Li and Cs from the residual melts, and their removal and migration away from the granite system, may be pivotal in the generation of the Li-rich pegmatites.</div></div>","PeriodicalId":19644,"journal":{"name":"Ore Geology Reviews","volume":"178 ","pages":"Article 106491"},"PeriodicalIF":3.2,"publicationDate":"2025-02-10","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143422416","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":2,"RegionCategory":"地球科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Records of high temperature ore fluids through magmatic vapor contraction from the Dongji gold deposit, SE China
IF 3.2 2区 地球科学 Q1 GEOLOGY Pub Date : 2025-02-10 DOI: 10.1016/j.oregeorev.2025.106495
Ming-Sen Fan , Pei Ni , Jun-Yi Pan , Jun-Ying Ding , Zhe Chi , Jian-Ming Cui , Zhi-Lin Cheng , Fei-Peng Fan , Guang-Shi Zheng
The Dongji Au deposit represents the largest gold deposit in the Zhenghe region of South China with a proven reserve of 12.5 t gold and 136 t Silver. The deposit occurs mostly in Upper Jurassic rhyolite porphyry and partly in volcaniclastic rocks and is controlled by NE trending breccia zone. Our investigations suggest that two distinct stages of gold mineralization occur at Dongji: the stage 1 is dominated by quartz, pyrite, and arsenopyrite, with visible Au − Ag minerals, and occurs as a wide variety of structural styles that include individual veins, fracture stockworks and breccias; and the late stage 2 is characterized by gold-bearing pyrite, illite, chalcedony, and apatite, mainly distributed in cement of breccia style ores. The host rocks near orebodies develop pronounced illitization, silicification, weak chloritization. Microthermometric results from fluid inclusions within multi-generation growth zones of quartz in stage 1 and secondary fractures associated with later stage yielded homogenization temperatures (320 ∼ 411℃ and 218 ∼ 332 ℃, respectively) and salinities (0.4 ∼ 4.2 wt% NaCl equivalents and 0.7 ∼ 3.9 wt% NaCl equivalents, respectively). Combined with quartz titanium thermometer results, the high temperature and low salinity ranges of liquid-rich two-phase fluid inclusion in quartz of stage 1 indicate that the ore-forming fluid originated from magmatic vapor, which contracted into an aqueous liquid by cooling at elevated lithostatic pressure above the critical curve of the salt-water fluid system. The δDV-SMOW values of stage1 quartz range from − 69.9 ‰ to − 60.9 ‰, with δ18OH2O‰ values between − 0.9 ‰ and 1.4 ‰, implying the auriferous fluids derive from a magmatic with minor meteoric mixed source. The δ34SV–CDT values of pyrite of stage 1 and 2 range from –0.3 to 8.0 ‰, revealing that sulfur mainly originates from the magma. The microthermometric data and quartz composition evolution suggest a fluid mixing contribution to metal precipitation. Combined with the geology, gangue and ore mineral assemblage, alteration, fluid inclusion, and H–O–S isotopic characteristics, we propose that the auriferous ore-forming fluids of the Dongji deposit may be the product of magma vapor contraction and migration in a porphyry–epithermal transitional gold system. These findings also indicate a great prospecting potential for the porphyry type mineralization at depth.
{"title":"Records of high temperature ore fluids through magmatic vapor contraction from the Dongji gold deposit, SE China","authors":"Ming-Sen Fan ,&nbsp;Pei Ni ,&nbsp;Jun-Yi Pan ,&nbsp;Jun-Ying Ding ,&nbsp;Zhe Chi ,&nbsp;Jian-Ming Cui ,&nbsp;Zhi-Lin Cheng ,&nbsp;Fei-Peng Fan ,&nbsp;Guang-Shi Zheng","doi":"10.1016/j.oregeorev.2025.106495","DOIUrl":"10.1016/j.oregeorev.2025.106495","url":null,"abstract":"<div><div>The Dongji Au deposit represents the largest gold deposit in the Zhenghe region of South China with a proven reserve of 12.5 t gold and 136 t Silver. The deposit occurs mostly in Upper Jurassic rhyolite porphyry and partly in volcaniclastic rocks and is controlled by NE trending breccia zone. Our investigations suggest that two distinct stages of gold mineralization occur at Dongji: the stage 1 is dominated by quartz, pyrite, and arsenopyrite, with visible Au − Ag minerals, and occurs as a wide variety of structural styles that include individual veins, fracture stockworks and breccias; and the late stage 2 is characterized by gold-bearing pyrite, illite, chalcedony, and apatite, mainly distributed in cement of breccia style ores. The host rocks near orebodies develop pronounced illitization, silicification, weak chloritization. Microthermometric results from fluid inclusions within multi-generation growth zones of quartz in stage 1 and secondary fractures associated with later stage yielded homogenization temperatures (320 ∼ 411℃ and 218 ∼ 332 ℃, respectively) and salinities (0.4 ∼ 4.2 wt% NaCl equivalents and 0.7 ∼ 3.9 wt% NaCl equivalents, respectively). Combined with quartz titanium thermometer results, the high temperature and low salinity ranges of liquid-rich two-phase fluid inclusion in quartz of stage 1 indicate that the ore-forming fluid originated from magmatic vapor, which contracted into an aqueous liquid by cooling at elevated lithostatic pressure above the critical curve of the salt-water fluid system. The δD<sub>V-SMOW</sub> values of stage1 quartz range from − 69.9 ‰ to − 60.9 ‰, with δ<sup>18</sup>O<sub>H2O</sub>‰ values between − 0.9 ‰ and 1.4 ‰, implying the auriferous fluids derive from a magmatic with minor meteoric mixed source. The δ<sup>34</sup>S<sub>V–CDT</sub> values of pyrite of stage 1 and 2 range from –0.3 to 8.0 ‰, revealing that sulfur mainly originates from the magma. The microthermometric data and quartz composition evolution suggest a fluid mixing contribution to metal precipitation. Combined with the geology, gangue and ore mineral assemblage, alteration, fluid inclusion, and H–O–S isotopic characteristics, we propose that the auriferous ore-forming fluids of the Dongji deposit may be the product of magma vapor contraction and migration in a porphyry–epithermal transitional gold system. These findings also indicate a great prospecting potential for the porphyry type mineralization at depth.</div></div>","PeriodicalId":19644,"journal":{"name":"Ore Geology Reviews","volume":"178 ","pages":"Article 106495"},"PeriodicalIF":3.2,"publicationDate":"2025-02-10","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143402839","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":2,"RegionCategory":"地球科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Stratigraphy, facies, and chemostratigraphy at the Palaeoproterozoic Rävliden North Zn-Pb-Ag-Cu VMS deposit, Skellefte district, Sweden
IF 3.2 2区 地球科学 Q1 GEOLOGY Pub Date : 2025-02-06 DOI: 10.1016/j.oregeorev.2025.106489
Filip Simán , Nils Jansson , Foteini Simistira Liwicki , Erik Nordfeldt , Mac Fjellerad Persson , Lena Albrecht , Christian Günther , Paul McDonnell , Tobias Hermansson
Many base and precious metals are sourced from volcanic massive sulphide (VMS) deposits and understanding the geological characteristics of such deposits is crucial for new discoveries of this deposit type. Although key geological characteristics of modern VMS systems are relatively well understood, a remaining challenge is resolving the same geological characteristics in ancient, complex, altered and metamorphosed VMS deposits. One such deposit is the Palaeoproterozoic Rävliden North deposit, an 8.7 Mt (combined resources and reserves of 3.42 % Zn, 0.90 % Cu, 0.54 % Pb, 81 g/t Ag, and 0.24 g/t Au) replacement-style volcanic massive sulphide deposit in the felsic-bimodal western Skellefte district, northern Sweden. The VMS deposits in the Skellefte district are hosted in rocks subjected to greenschist to amphibolite facies metamorphism and occur at the lithostratigraphic contact between the metavolcanic 1.89 – 1.88 Ga Skellefte group (SG) and stratigraphically overlying metasiliciclastic 1.89 – 1.87 Ga Vargfors group (VG). Intense hydrothermal alteration commonly eradicates original rock textures, and polyphase deformation and metamorphism make geological interpretation and stratigraphic reconstruction difficult. Hence, to complement lithofacies analysis, immobile element chemostratigraphy is used in this study.
Rävliden North is predominantly hosted by felsic volcanic rocks of the herein defined Rävliden formation in the upper part of the SG that were deposited in half grabens related to rifting of a continental arc. Based on immobile elements and their ratios the felsic rocks fall into three groups, Rhy I, II and III. The chemostratigraphy and lithostratigraphy roughly coincide, where Rhy II (Zr/Al2O3 = 12.86, Al2O3/TiO2 = 36.07, Zr/TiO2 = 0.05) defines the rhyolites beneath the Rävliden formation that predominantly comprises Rhy I (Zr/Al2O3 = 17.23, Al2O3/TiO2 = 32.33, Zr/TiO2 = 0.06) and Rhy III (Zr/Al2O3 = 17.95, Al2O3/TiO2 = 36.53, Zr/TiO2 = 0.07), where Rhy I is the chief host to mineralisation. Mineralisation is partially hosted by graphitic phyllite that overlies the Rävliden formation and represents the base of the VG that indicates paused volcanism important for the build-up of massive sulphides beneath the seafloor. Facies analysis of rhyolites suggest that these were unconsolidated pumice rich rocks permeable for the upwelling hydrothermal fluids. Additionally, graphitic phyllite functioned as a permeability barrier inducing lateral fluid flow resulting in more effective sulphide precipitation.
This study demonstrates the effectiveness of combining stratigraphic, facies and chemostratigraphic analysis for targeting VMS deposits in complex, altered and metamorphosed rocks.
{"title":"Stratigraphy, facies, and chemostratigraphy at the Palaeoproterozoic Rävliden North Zn-Pb-Ag-Cu VMS deposit, Skellefte district, Sweden","authors":"Filip Simán ,&nbsp;Nils Jansson ,&nbsp;Foteini Simistira Liwicki ,&nbsp;Erik Nordfeldt ,&nbsp;Mac Fjellerad Persson ,&nbsp;Lena Albrecht ,&nbsp;Christian Günther ,&nbsp;Paul McDonnell ,&nbsp;Tobias Hermansson","doi":"10.1016/j.oregeorev.2025.106489","DOIUrl":"10.1016/j.oregeorev.2025.106489","url":null,"abstract":"<div><div>Many base and precious metals are sourced from volcanic massive sulphide (VMS) deposits and understanding the geological characteristics of such deposits is crucial for new discoveries of this deposit type. Although key geological characteristics of modern VMS systems are relatively well understood, a remaining challenge is resolving the same geological characteristics in ancient, complex, altered and metamorphosed VMS deposits. One such deposit is the Palaeoproterozoic Rävliden North deposit, an 8.7 Mt (combined resources and reserves of 3.42 % Zn, 0.90 % Cu, 0.54 % Pb, 81 g/t Ag, and 0.24 g/t Au) replacement-style volcanic massive sulphide deposit in the felsic-bimodal western Skellefte district, northern Sweden. The VMS deposits in the Skellefte district are hosted in rocks subjected to greenschist to amphibolite facies metamorphism and occur at the lithostratigraphic contact between the metavolcanic 1.89 – 1.88 Ga Skellefte group (SG) and stratigraphically overlying metasiliciclastic 1.89 – 1.87 Ga Vargfors group (VG). Intense hydrothermal alteration commonly eradicates original rock textures, and polyphase deformation and metamorphism make geological interpretation and stratigraphic reconstruction difficult. Hence, to complement lithofacies analysis, immobile element chemostratigraphy is used in this study.</div><div>Rävliden North is predominantly hosted by felsic volcanic rocks of the herein defined Rävliden formation in the upper part of the SG that were deposited in half grabens related to rifting of a continental arc. Based on immobile elements and their ratios the felsic rocks fall into three groups, Rhy I, II and III. The chemostratigraphy and lithostratigraphy roughly coincide, where Rhy II (Zr/Al<sub>2</sub>O<sub>3</sub> = 12.86, Al<sub>2</sub>O<sub>3</sub>/TiO<sub>2</sub> = 36.07, Zr/TiO<sub>2</sub> = 0.05) defines the rhyolites beneath the Rävliden formation that predominantly comprises Rhy I (Zr/Al<sub>2</sub>O<sub>3</sub> = 17.23, Al<sub>2</sub>O<sub>3</sub>/TiO<sub>2</sub> = 32.33, Zr/TiO<sub>2</sub> = 0.06) and Rhy III (Zr/Al<sub>2</sub>O<sub>3</sub> = 17.95, Al<sub>2</sub>O<sub>3</sub>/TiO<sub>2</sub> = 36.53, Zr/TiO<sub>2</sub> = 0.07), where Rhy I is the chief host to mineralisation. Mineralisation is partially hosted by graphitic phyllite that overlies the Rävliden formation and represents the base of the VG that indicates paused volcanism important for the build-up of massive sulphides beneath the seafloor. Facies analysis of rhyolites suggest that these were unconsolidated pumice rich rocks permeable for the upwelling hydrothermal fluids. Additionally, graphitic phyllite functioned as a permeability barrier inducing lateral fluid flow resulting in more effective sulphide precipitation.</div><div>This study demonstrates the effectiveness of combining stratigraphic, facies and chemostratigraphic analysis for targeting VMS deposits in complex, altered and metamorphosed rocks.</div></div>","PeriodicalId":19644,"journal":{"name":"Ore Geology Reviews","volume":"178 ","pages":"Article 106489"},"PeriodicalIF":3.2,"publicationDate":"2025-02-06","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143395168","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":2,"RegionCategory":"地球科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
期刊
Ore Geology Reviews
全部 Acc. Chem. Res. ACS Applied Bio Materials ACS Appl. Electron. Mater. ACS Appl. Energy Mater. ACS Appl. Mater. Interfaces ACS Appl. Nano Mater. ACS Appl. Polym. Mater. ACS BIOMATER-SCI ENG ACS Catal. ACS Cent. Sci. ACS Chem. Biol. ACS Chemical Health & Safety ACS Chem. Neurosci. ACS Comb. Sci. ACS Earth Space Chem. ACS Energy Lett. ACS Infect. Dis. ACS Macro Lett. ACS Mater. Lett. ACS Med. Chem. Lett. ACS Nano ACS Omega ACS Photonics ACS Sens. ACS Sustainable Chem. Eng. ACS Synth. Biol. Anal. Chem. BIOCHEMISTRY-US Bioconjugate Chem. BIOMACROMOLECULES Chem. Res. Toxicol. Chem. Rev. Chem. Mater. CRYST GROWTH DES ENERG FUEL Environ. Sci. Technol. Environ. Sci. Technol. Lett. Eur. J. Inorg. Chem. IND ENG CHEM RES Inorg. Chem. J. Agric. Food. Chem. J. Chem. Eng. Data J. Chem. Educ. J. Chem. Inf. Model. J. Chem. Theory Comput. J. Med. Chem. J. Nat. Prod. J PROTEOME RES J. Am. Chem. Soc. LANGMUIR MACROMOLECULES Mol. Pharmaceutics Nano Lett. Org. Lett. ORG PROCESS RES DEV ORGANOMETALLICS J. Org. Chem. J. Phys. Chem. J. Phys. Chem. A J. Phys. Chem. B J. Phys. Chem. C J. Phys. Chem. Lett. Analyst Anal. Methods Biomater. Sci. Catal. Sci. Technol. Chem. Commun. Chem. Soc. Rev. CHEM EDUC RES PRACT CRYSTENGCOMM Dalton Trans. Energy Environ. Sci. ENVIRON SCI-NANO ENVIRON SCI-PROC IMP ENVIRON SCI-WAT RES Faraday Discuss. Food Funct. Green Chem. Inorg. Chem. Front. Integr. Biol. J. Anal. At. Spectrom. J. Mater. Chem. A J. Mater. Chem. B J. Mater. Chem. C Lab Chip Mater. Chem. Front. Mater. Horiz. MEDCHEMCOMM Metallomics Mol. Biosyst. Mol. Syst. Des. Eng. Nanoscale Nanoscale Horiz. Nat. Prod. Rep. New J. Chem. Org. Biomol. Chem. Org. Chem. Front. PHOTOCH PHOTOBIO SCI PCCP Polym. Chem.
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
0
微信
客服QQ
Book学术公众号 扫码关注我们
反馈
×
意见反馈
请填写您的意见或建议
请填写您的手机或邮箱
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
现在去查看 取消
×
提示
确定
Book学术官方微信
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术
文献互助 智能选刊 最新文献 互助须知 联系我们:info@booksci.cn
Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。
Copyright © 2023 Book学术 All rights reserved.
ghs 京公网安备 11010802042870号 京ICP备2023020795号-1