Search Results (5)

The Mesoproterozoic (~1470 Ma) Wolf River batholith (WRB) is exposed over 6500 km², encompassing 11 plutons that crosscut the Archean Marshfield and Proterozoic Penokean terranes. As the WRB is the classically defined anorogenic batholith, to test this hypothesis, seven igneous phases were analyzed using anisotropy of magnetic susceptibility (AMS), as a proxy for magmatic flow during intrusion, and the samples recorded a sub-horizontal emplacement in six different orientations. Paleopoles from six of eight igneous samples preserve a wide variety of sub-vertical orientations with two reversed and four normal polarities. The synorogenic Baldwin Conglomerate is the youngest rock (<1460 Ga) associated with WRB. Magnetic fabrics are horizontal, but multidomain and paleopole signatures, where interpretable, are sub-vertical. The North American APWP places middle Laurentia at low-latitude during Geon 14, and all our paleopoles are sub-vertical, not sub-horizontal, again suggesting post-intrusion deformation. Moreover, the McCauley gneiss (1886 Ma; U-Pb zircon), Rib Mountain Quartzite (1750 Ma MDA; U-Pb zircon, n = 150), Dells of the Eau Claire rhyolite (1483 Ma; U-Pb zircon, 1469 Ma; monazites-in-garnet), and Baldwin conglomerate (1460 Ma MDA; U-Pb zircons, n = 150) are sub-vertical inliers (xenoliths) in the igneous suite; the Proterozoic Wausau turbidite (1850 Ma MDA; U-Pb zircon, n = 150) was intruded by the WRB and dips 25°W. Here, we present a reinterpretation of the WRB as a deformed synorogenic rather than an anorogenic intrusion. Full article

Gold occurrence Maljavr is the first Archean conglomerate-hosted gold mineralization found in the Fennoscandian Shield. Gold-mineralized metasomatic rocks form a set of lenses within a 10 m thick linear zone, conformable to the bedding of host conglomerates. The lenses are up to 10 m long and up to 1 m thick and they clearly exhibit three alteration envelopes: the rock in the central part consists of garnet and quartz or garnet-only; biotite, garnet, and quartz make the intermediate biotite–garnet envelope; hornblende, hedenbergite, and quartz are the principal rock-forming minerals in the outer zone of the lenses. All metasomatic rocks contain sulfide mineralization up to 15–20 vol.% and up to 0.6 g/t Au. The main ore mineral is pyrrhotite, and the minor minerals are arsenopyrite, chalcopyrite, pentlandite, löllingite, and troilite. The age of zircon from biotite gneiss in the zone of alteration is 2664 ± 18 Ma, this is considered as the time of formation of lenses of metasomatic rocks. Biotite gneiss-conglomerate and metasomatic rocks were later intruded by tourmaline granite pegmatite 2508 ± 7 Ma. The injection of pegmatite caused re-crystallization of sulfides (mainly arsenopyrite and löllingite) and redistribution of gold. Visible gold in association with Bi minerals native bismuth, ehrigite, maldonite, bismuthinite, joseite-B, and hedleyite was found in inclusions in recrystallized arsenopyrite and löllingite. Au content in the rocks with recrystallized arsenopyrite and löllingite is >1 g/t, up to 30 g/t in hand samples. The 2508 Ma pegmatite is interpreted as synchronous with formation of gold mineralization in its present form. The linkage of gold mineralization with pegmatite and geochemical association Au-As-Se-Te-Bi in the mineralized rocks agree with characteristics of intrusion-related gold deposits worldwide. Biotite gneiss–metaconglomerate, hosting the mineralized altered rocks, was the probable primary source of arsenic and gold for mineralization. Full article

Possible young analogues for regionally extensive unconformities (100 to 400 km²) in the gold-bearing Witwatersrand Supergroup (Archean, South Africa) occur in the South Island of New Zealand. Extensive marine unconformities in New Zealand show progression from an unconformity surface to conglomerate to clean well-sorted sandstone to marine mudstone, as is also found in the major Witwatersrand auriferous reef horizons. The hosting young sedimentary basins of the South Island rest on thin or thick crust on inboard and outboard foreland settings, with variable alluvial gold budgets. They expose the Cretaceous–Oligocene Waipounamu Erosion Surface unconformity that formed when most of New Zealand was subsiding, and Pleistocene–Holocene unconformities related to global sea level changes. The Witwatersrand gold-bearing reef sediments are a good match for such marine transgressions, but not alluvial fans or braided streams. Most Witwatersrand gold is immediately above planar unconformity surfaces and not restricted to, or concentrated in, erosion channels that are incised through the reefs. However, in modern alluvial fans or braided streams, gold is almost entirely in erosion channels on a smaller scale than the Witwatersrand gold reef packages and not spread across the planar unconformities. Alluvial fans and braid plains in New Zealand dilute gold with large volumes of gravel. Full article

In China, pre-Quaternary solid potash deposit has only been discovered in the Simao Basin, and the Lower Cretaceous Mengyejing (MYJ) Formation (Fm.) is the productive layer of potash deposit. In this study, we investigated the clay conglomerates which are distributed in upper and lower members of the potash-bearing salt rock layer. We analyzed the relative contents of major elements (Al₂O₃, Fe₂${\mathrm{O}}_3^{\mathrm{T}}$, MgO, CaO, Na₂O, K₂O) and trace elements (B, Ba, Co, Cr, Cu, Ga, Mn, Ni, Rb, Sr, V, Zn, Zr) in the samples. The results show that MgO and CaO in the major elements are rich relative to Post Archean Australian Shale (PAAS), whose average enrichment factor values of the MgO (EF_MgO) is 2.61 and CaO (EF_CaO) is 4.57, and the others major elements are relatively minor; trace elements (B, Ga, Mn, Zr) are rich relative to PAAS, and the others trace elements are minor relative to PAAS. The study of paleogeographic conditions using various parameters shows that the paleoclimate is generally dry and hot during the period of clay conglomerate deposition, but it was warm and humid in certain periods; the main sedimentary environment is weak oxidation condition with strong oxidation conditions in individual periods; the average value of paleosalinity is ~21‰, and the highest is no more than ~92‰. The significance of the paleogeographic characteristics of MYJ Fm. to potash mineralization are as follows: (1) they indicates that the clay conglomerates of MYJ Fm. are not clastic sediments in brine formed by seawater, because the paleosalinity of clay conglomerates deposition period is obviously lower than that of seawater; (2) MYJ potassic salt ore is not formed by evaporation and concentration of seawater in clay conglomerates in the sedimentary basin, because there is no carbonate rock and sulfate rock of corresponding scale after the deposition of clay conglomerates in the basin; (3) clay conglomerates of MYJ Fm. were deposited in continental shallow water basin; (4) the matter source of potash minerals is deep marine strata; (5) in the MYJ Fm. sedimentation period, deep source salt moved to the surface under the background of extensional structure, and the subsequent sedimentary clastic rock formed a protective layer of potash-bearing rock, thus completing the “deep source and shallow mineralization” metallogenic process. Full article

With new advances in rapid-acquisition geochemical and hyperspectral techniques, exploration companies are now able to detect subtle halos surrounding orebodies at minimal expense. The Nimbus Ag-Zn-(Au) deposit is unique in the Archean Yilgarn Craton of Western Australia. Due to its mineralogy, alteration assemblages, geochemical affinity, and tectonic setting, it is interpreted to represent a shallow water (~650 mbsl) and low-temperature (<250 °C) volcanogenic massive sulfide (VMS) deposit with epithermal characteristics (i.e., a hybrid bimodal felsic deposit). We present a detailed paragenetic account of the Nimbus deposit, and establish lithogeochemical and hyperspectral halos to mineralization to aid exploration. Mineralization at Nimbus is characterized by early units of barren massive pyrite that replace glassy dacitic lavas, and underlying zones of polymetallic sulfides that replace autoclastic monomict dacite breccias. The latter are dominated by pyrite-sphalerite-galena, a diverse suite of Ag-Sb ± Pb ± As ± (Cu)-bearing sulfosalts, minor pyrrhotite, arsenopyrite, and rare chalcopyrite. The main sulfosalt suite is characterized by pyrargyrite, and Ag-rich varieties of boulangerite, tetrahedrite, and bournonite. Zones of sulfide mineralization in quartz-sericite(±carbonate)-altered dacite are marked by significant mass gains in Fe, S, Zn, Pb, Sb, Ag, As, Cd, Ni, Cu, Ba, Co, Cr, Tl, Bi, and Au. Basaltic rocks show reduced mass gains in most elements, with zones of intense quartz-chlorite-carbonate±fuchsite alteration restricted to thick sequences of hyaloclastite, and near contacts with dacitic rocks. Broad zones of intense silica-sericite alteration surround mineralization in dacite, and are marked by high Alteration Index and Chlorite-Carbonate-Pyrite Index (CCPI) values, strong Na-Ca depletion, and an absence of feldspar (albite) in thermal infrared (TIR) data. White mica compositions are predominantly muscovitic in weakly altered sections of the dacitic footwall sequence. More paragonitic compositions are associated with zones of increased sericitization and high-grade polymetallic sulfide mineralization. Chlorite in dacitic rocks often occurs adjacent to zones of sulfide mineralization and is restricted to narrow intervals. Carbonate abundance is sporadic in dacite, but is most abundant outside the main zones of Na-Ca depletion. Basaltic rocks are characterized by strongly paragonitic white mica compositions, and abundant chlorite and carbonate. Shifts from Ca carbonates and Fe-rich chlorites to more Mg-rich compositions of both minerals occur in more intensely hydrothermally altered basaltic hyaloclastite, and near contacts with dacitic rocks. Hanging-wall polymict conglomerates are characterized by minor amounts of muscovitic to phengitic white mica (2205–2220 nm), and an absence of chlorite and carbonate alteration. Full article