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The Laird Lake property, southwest Red Lake greenstone belt, straddles the contact between the Balmer (2.99–2.96 Ga) and the Confederation (2.74–2.73 Ga) assemblages. The property is 10 km along strike from the Madsen and Starrat–Olsen Au mines that are hosted near the contact. The Balmer assemblage consists of fine-grained, aphyric, locally pillowed mafic volcanic rocks, ultramafic intrusive and volcanic rocks with flow breccia textures hosting local spinifex-bearing clasts, and banded-iron formations. In contrast, the Confederation assemblage comprises porphyritic mafic volcanic rocks intercalated with intermediate to felsic volcanic rocks that include crystal lapilli tuffs, crystal tuffs, and tuffs. The Balmer assemblage is composed of tholeiitic mafic volcanic rocks with minor Al-undepleted komatiites, whereas the Confederation assemblage is calc–alkalic. Neodymium isotopes, in conjunction with trace element geochemistry, suggests that parts of the Balmer assemblage were weakly contaminated by an older intermediate basement. Both arc and back-arc volcanism occurs in the Confederation assemblage, with the arc rocks showing a stronger crustal component than the back-arc rocks. A maximum U–Pb age of 2741 ± 19 Ma for a crystal tuff and an age of 2737.68 ± 0.79 Ma for a diorite are consistent with a Confederation assemblage affinity for the intermediate calc–alkaline rocks south of the Au-bearing horizon. The Balmer assemblage represents an oceanic plateau formed by plume magmatism on the margins of the North Caribou Terrane, whereas the Confederation assemblage at Laird Lake formed in an oceanic arc setting where both arc and back-arc volcanism occurred simultaneously. [ABSTRACT FROM AUTHOR]

The St. Ignace Island complex in Northern Ontario is a package of dominantly felsic rocks emplaced within the upper portions of the Osler Volcanic rocks of the ~1.1 Ga Midcontinent Rift System. The Osler volcanic rocks are predominantly tholeiitic basalts intercalated with rare interflow sediments and rhyolites. The St. Ignace Island complex is an ~26-km2 stock with a felsic core of quartz–feldspar–phyric rhyolites and dacites and an outer ring of anorthosite and gabbro. Textures at a variety of scales within the rocks of the complex show clear evidence of the mingling and mixing of partially crystallized mafic and felsic liquids. Two multigrain (zircon/baddeleyite) fractions from a sample of the gabbro define a Discordia line with an upper intercept date of 1107 ± 8.9 Ma. The core of the complex consists of dacites and rhyolites with similar REE abundances with negative Nb anomalies, whereas the surrounding mafic rocks are gabbros to monzogabbros that are less LREE-enriched than the felsic rocks but with similar HREE. Felsic units have a narrow range of 87Sr/86Sri (0.7032–0.7045) and 143Nd/144Ndi (0.51051–0.51057), whereas the mafic end members have similar 87Sr/86Sri (0.7040–0.7061) but more radiogenic 143Nd/144Ndi (0.51067–0.51085). Very well-preserved silicate melt inclusions (MI), many completely glassy, were observed in quartz, clinopyroxene, and some plagioclase phenocrysts from the complex. These represent some of the oldest unrecrystallized silicate melt inclusions described to date. Melt inclusions within quartz from the felsic volcanics are broadly rhyolitic in composition, whereas MI from plagioclase in the mafic volcanics range from basalt to basaltic andesite; these felsic and mafic melt compositions are interpreted to represent the end-member liquids in the system and bulk rock analyses affirm mixtures of the two. Concentrations of Cu and Ag (in both mafic and felsic MI), and Mo (in felsic MI), are up to an order of magnitude higher in the mafic and felsic MI than in continental crust. Bulk rock metal concentrations are also significantly lower than in the MI, suggesting that the melt inclusions may preserve pre-eruptive metal tenors that were subsequently modified by sulfide saturation, degassing, or post-solidus hydrothermal alteration. The whole rock and MI geochemistry of the St. Ignace complex are broadly similar to the Central Osler Group and, given the broad similar ages, suggests they may have been derived from a similar mantle source, but distinct from the source of rhyolites in the Black Bay Peninsula. The negative Nb anomalies and negative εNd values for the St. Ignace complex are consistent with mixing with older continental crust during ascent and emplacement. The rocks of the St. Ignace Island complex likely formed as the result of emplacement of a large mafic magma chamber at the base of the Osler volcanic pile that triggered partial melting to generate the rhyolite end members. The felsic melts ascended to shallower levels in the crust where they mixed with mafic magmas derived directly from the deeper chamber. Generally, melt inclusions in the complex have very high Cu and Ag contents, similar to those observed in arc-related and extremely oxidized early rift-related rocks and may account for the world-class volcano-sediment-hosted Cu–(Ag) deposits within the rift and the presence of small porphyry-style deposits. [ABSTRACT FROM AUTHOR]

Stratabound ore has been recognized as an end-member of porphyry copper systems, but pyrite chemistry has not been widely applied to linking stratabound ore with the related porphyry and skarn system. Stratabound ore is commonly developed around porphyry-skarn systems in eastern China, and is characterized by abundant colloform pyrite; however the origin of the colloform pyrite has been contentious. Xinqiao deposit is ideal for study of pyrite geology and geochemistry with the aim of elucidating formation of the stratabound ore and to decipher the evolution of pyrite compositions in a porphyry-skarn environment. The colloform pyrite paragenesis and S isotopes indicate that it formed during early skarn mineralization, based on its occurrence in stockwork veins cutting skarn minerals, and that it is replaced by later hypogene sulfides; the δ34S of colloform pyrite (average 6.12‰) is close to the δ34S value of both porphyry- (average 5.06‰) and skarn-type pyrite (average 4.65‰). The colloform texture formed as an aggregate of nanometer- or micrometer-sized (<0.2 μm) pyrite cubes produced by rapid crystallization from a high-fS2, low-temperature, and supersaturated fluid. Supersaturation of the fluid was probably produced by rapid decompression that triggered fluid boiling and cooling when the magmatic-hydrothermal fluid (derived from Cretaceous magma) flowed along the Devonian-Carboniferous unconformity. Subsequently, the colloform pyrite was replaced by later stage pyrite with distinctive trace elements (Co, Ni, and Se), indicating that the stratabound ore at Xinqiao formed from multiple pulses of magmatic-hydrothermal fluids derived from an Early Cretaceous stock. Co, Ni, and Se enrichment in porphyry- and proximal skarn-type pyrite suggests they formed at relatively high temperature, whereas the colloform pyrite shows trace element contents (Cu, Pb, Zn, Ag, and Bi) similar to those in distal skarn pyrite, suggesting that they may have formed in the same fluid environment. The trace element variations in pyrite from stratabound, skarn and porphyry ore probably resulted from decreasing fluid temperature and increasing pH away from the source. Our data, combined with previous studies, show that Co and Ni in pyrite increase toward porphyry and skarn ore, whereas As, Sb, Pb, Ag, and Bi are enriched in pyrite in distal stratabound ore, which extends for 1–2 km away from the intrusion. A plot of As/Se vs. Co discriminates the three ore types that occur associated with porphyry-skarn Cu systems in the Middle and Lower Yangtze belt (MLYB). These results indicate pyrite chemistry can be effective in discriminating the genesis of different deposit types related to porphyry-skarn systems and can potentially be used as a vectoring tool during exploration in the MLYB and elsewhere. [ABSTRACT FROM AUTHOR]

Scheelite from the Tongshankou porphyry-skarn Cu-Mo(-W) deposit occurs mainly as disseminated grains in the altered granodiorite porphyries at depth (Sch A), in the skarn coeval with retrograde al- teration (Sch B) and in distal quartz veins crosscutting marbles (Sch C). Cathodoluminescence (CL) responses within a single Sch A grain reveal two subtypes: CL-clear Sch A-I and CL-turbid, densely veined Sch A-II. The CL contrast, coupled with geochemical data, suggest Sch A-I was metasomatized to form Sch A-II. CL images reveal that Sch A-I, Sch B and Sch C are all homogenous, with blue luminescence and are depleted in heavy rare earth elements (HREE), indicating a primary origin. However, Sch A-II is characterized by higher contents of light REE and heavy REE as well as higher Sr isotopes (0.7080-0.7100) than the primary scheelite (<0.7080). These differences indicate that Sch A-II formed through dissolution-reprecipitation. The Sr isotopes of the primary scheelite (0.7073-0.7078) are generally consistent with those of the mineralized granodiorite porphyries (0.7061-0.7063) and mafic enclaves (0.7058-0.7073). The granodiorite porphyries contain low tungsten contents (3-11 ppm), whereas high tungsten contents were detected in mafic enclaves (48-75 ppm). The coexistence of mafic enclaves and tungsten mineralization at depth, and their consistent Sr isotopes, indicates that the interaction of mafic enclaves and exsolved magmatic fluids from the granodiorite porphyries may have played an important role in the extraction of tungsten from the mafic enclaves and formation of scheelite mineralization. Our work shows that scheelite geochemistry can be used to trace the mineralizing conditions but the compositions may be significantly modified during the ore-forming process. Thus, detailed textural relationships should be investigated before using scheelite geochemistry to constrain the hydrothermal fluids and ore genesis. [ABSTRACT FROM AUTHOR]

Copyright of Canadian Journal of Earth Sciences is the property of Canadian Science Publishing and its content may not be copied or emailed to multiple sites or posted to a listserv without the copyright holder's express written permission. However, users may print, download, or email articles for individual use. This abstract may be abridged. No warranty is given about the accuracy of the copy. Users should refer to the original published version of the material for the full abstract. (Copyright applies to all Abstracts.)

The Lake Nipigon Region Geoscience Initiative (LNRGI) was a 3-year collaborative geoscience data acquisition and compilation project that focussed on Lake Nipigon in Ontario and involved partnerships between mineral industry, university, and provincial and federal government geoscientists. A major objective of the initiative was to collect new geoscience information to better understand the geological history of the Nipigon region to inform land-use planning, identify areas of high mineral potential, and attract mineral exploration. The Special Issue on the LNRGI highlights the scientific successes of the Initiative in the fields of geology, petrology, geochemistry, geochronology, stratigraphy and basin analysis, mineral deposits, and surficial geology and geochemistry. [ABSTRACT FROM AUTHOR]

Copyright of Canadian Journal of Earth Sciences is the property of Canadian Science Publishing and its content may not be copied or emailed to multiple sites or posted to a listserv without the copyright holder's express written permission. However, users may print, download, or email articles for individual use. This abstract may be abridged. No warranty is given about the accuracy of the copy. Users should refer to the original published version of the material for the full abstract. (Copyright applies to all Abstracts.)

The Mesoproterozoic 1108–1105 Ma Osler Group, a 3 km thick succession of basaltic flows and sedimentary units on the north shore of Lake Superior, is among the oldest expressions of the Midcontinent Rift. Basal sediments of the Simpson Island Formation (new name) deposited by braided fluvial systems record westward transport of debris eroded from local Archean and Proterozoic rock units. Strata deposited by this fluvial system are intercalated with, and overlain by, ocean-island basalt (OIB)-like basalts, which become increasingly contaminated up section (εNd(1100Ma) = +0.3 to –5.3). The light rare-earth element (LREE) enriched (La/Smn = 1.5–3.9) and heavy REE (HREE) fractionated (Gd/Ybn = 1.5–3.7) subaerial flows are divisible into two units that correlate with other sections of the Osler Group to the east, but simple correlations with more distant sequences are difficult. The volcanic rock dominated portion of the succession is overlain by a thin (25 m thick) conglomerate–sandstone assemblage representing southeast progradation of an alluvial fan in a semi-arid climatic setting. Clast lithologies and geochemistry indicate no extra-rift detritus was delivered from the hinterland of the fan. Various lines of evidence in both volcanic and sedimentary rocks support a scenario where early, pre-1108 Ma, subsidence along a north–south axis from the western arm of the rift to the Nipigon Embayment was replaced by subsidence along the east–west rift axis between 1108 and 1105 Ma. [ABSTRACT FROM AUTHOR]

The Mesoproterozoic English Bay Complex consists of a granite-rhyolite assemblage outcropping on the shores of Lake Nipigon in western Superior Province, Canada. It intrudes Neoarchean rocks and is disconformably overlain by a rift–infracratonic basin sedimentary succession recording subsidence following a heating event. The granites and rhyolites are characterized by light rare-earth element (LREE) enrichment (La/Smn = 2.8–5.1) and only weakly fractionated heavy REE (HREE; Gd/Ybn = 1.1–1.6). The felsic igneous rocks are high-K, enriched in Zr, Nb, Y, and REE satisfying all the criteria for an A-type suite. Trace element geochemistry, particularly the absence of any negative Nb anomalies, indicates this melt did not originate in a suprasubduction zone setting, unlike the St. Francois Mountain Complex to the south. The English Bay Complex may record the northern portion of a Mesoproterozoic plume track— a plume that possibly led to earlier igneous activity and infracratonic basin formation to the north and would later interact with a suprasubduction zone margin to the south. [ABSTRACT FROM AUTHOR]

The origin of stratabound deposits in the Middle-Lower Yangtze River Valley Metallogenic Belt (MLYRB), Eastern China, is the subject of considerable debate. The Xinqiao Cu-Fe-Au deposit in the Tongling ore district is a typical stratabound ore body characterized by multi-stage magnetite. A total of six generations of magnetite have been identified. Mt1 is commonly replaced by porous Mt2, and both are commonly trapped in the core of Mt3, which is characterized by both core-rim textures and oscillatory zoning. Porous Mt4 commonly truncates the oscillatory zoning of Mt3, and Mt5 is characterized by 120° triple junction texture. Mt1 to Mt5 are commonly replaced by pyrite that coexists with quartz, whereas Mt6, with a fine-grained foliated and needle-like texture, commonly cuts the early pyrite as veins and is replaced by pyrite that coexists with calcite. The geochemistry of the magnetite suggests that they are hydrothermal in origin. The microporosity of Mt2 and Mt4 magnetite, their sharp contacts with Mt1 and Mt3, and lower trace-element contents (e.g., Si, Ca, Mg, and Ti) than Mt1 and Mt3 suggest that they formed via coupled dissolution and reprecipitation of the precursor Mt1 and Mt3 magnetite, respectively. This was likely caused by high-salinity fluids derived from intensive waterrock interaction between the magmatic-hydrothermal fluids associated with the Jitou stock and Late Permian metalliferous black shales. The 120° triple junction texture of Mt5 suggests it is the result of fluid-assisted recrystallization, whereas Mt6 formed by replacement of hematite as a result of fracturing. The geochemistry of the magnetite suggests that the temperature increased from Mt2 to Mt3 and implies that there were multiple pulses of fluids from a magmatic-hydrothermal system. Therefore, we propose that the Xinqiao stratiform mineralization was genetically associated with multiple influxes of magmatic hydrothermal fluids derived from the Early Cretaceous Jitou stock. This study demonstrates that detailed texture examination and in situ trace-elements analysis under robust geological and petrographic frameworks can effectively constrain the mineralization processes and ore genesis. [ABSTRACT FROM AUTHOR]

[Display omitted] • Six types of pyrite formed in two overprinting gold-mineralizing events. • Monazite U-Pb dating constrains the age of early mineralization to ca. 429 Ma. • Distinct δ34S values suggest early metasedimentary and late magmatic origin of sulfur. The Tanjianshan goldfield is the most important gold producer in the North Qaidam, NW China. Genesis of gold deposits in Tanjianshan is enigmatic, primarily because of uncertainties as to timing, mineralization processes and fluid sources. We investigate these uncertainties through a comprehensive study of the texture and geochemistry (LA-MC-ICPMS trace elements and sulfur isotopes) of pyrite and in-situ U-Pb dating of monazite from the Qinglonggou gold deposit. Six types of pyrite with distinct textures, trace element contents and sulfur isotopes have been identified, and provide constraints on two overprinting gold-related hydrothermal events. Stage I consists of Py1, occurring as veinlets parallel to S1 deformation in a schist, is characterized by extremely low Co/Ni ratios with high contents of Ni, and high δ34S values (+14.9 ‰ to +16.1 ‰), and were likely derived from metamorphism of the sedimentary strata in the Tanjianshan and Wandonggou Group. In stage II, Py2 occurs in the pyrite-quartz veins that cut Py1 veinlets. They have similar δ34S (+13.1 ‰ to +17.8 ‰) to Py1, indicating that sulfur was likely derived from the dissolution of Py1. The stage I and II veins formed during an early gold pre-concentration event, which is constrained at 429.1 ± 5.9 Ma by in-situ U-Pb dating of monazite that coexists with Py1. Stage III includes Py3 and Py4 which occur in the altered carbonaceous schist and accompanying quartz veins. Trace metals are highest in Py3 (Ag, Au, Sb, and Bi) which represent the most economic ore stage in the deposit, whereas the following Py4 shows low concentrations of most trace elements due to abundant Py3 precipitation. In contrast, trace elements contents increase in Py5 to similar levels as those seen in Py3, suggesting a new pulse of fluid in stage IV. Minor Py6 grains precipitated in the youngest quartz-calcite veins associated with stage V, and contain low concentrations of trace elements. The δ34S values of Py3 (+5.2 ‰ to +6.0 ‰) and Py4 (+4.2 ‰ to +6.1 ‰) are within the range of magmatic sulfur, suggesting a dominantly magmatic source. The δ34S values increase from Py3-4 to Py5 (+6.3 ‰ to +7.4 ‰), and to Py6 (+8.7 ‰ to +9.6 ‰), probably due to increasing contribution from the host rocks, as well as decreasing f O 2 , through incremental fluid-rock interaction. Stages III and IV represent a late gold-mineralizing event during Late Paleozoic to Early Mesozoic, while stage V is post-mineralization. The overprinting gold pre-concentration and mineralization events in the Tanjianshan goldfield correspond to orogenic evolution of the Proto-Tethys Ocean and Paleo-Tethys Ocean, respectively. [ABSTRACT FROM AUTHOR]