scispace - formally typeset
Search or ask a question

Showing papers by "Simon E. Jackson published in 2022"


Journal ArticleDOI
TL;DR: In this article , a laser ablation-inductively coupled plasma mass spectrometry (LA-ICP-MS) U-Pb dating of hydrothermal calcite associated with the waning stage of mineralization is used to constrain the age of Neoproterozoic-hosted Carlin-type gold deposits in central Yukon, Canada.
Abstract: Laser ablation-inductively coupled plasma-mass spectrometry (LA-ICP-MS) U-Pb dating of hydrothermal calcite associated with the waning stage of mineralization is used to constrain the age of Neoproterozoic-hosted Carlin-type gold deposits in central Yukon, Canada. Samples exhibiting minor textural complexity show low dispersion of individual spot analyses and define Tera-Wasserburg lower intercept ages between 75.1 ± 2.5 and 71.2 ± 4.3 Ma. Samples with U-rich microfractures and/or a second generation of calcite associated with vein reopening record the primary stage of calcite growth related to hydrothermal activity at ca. 74 Ma and a younger ca. 48 Ma event related to fluid-assisted U mobility. The minimum age for mineralization at ca. 74 Ma overlaps with a maximum age based on a zircon U-Pb date of 74.1 ± 1.0 Ma for a gabbro dike that is locally altered and mineralized. These time constraints indicate that mineralization is ca. 74 Ma and penecontemporaneous with dike emplacement. Furthermore, mineralization is contemporaneous with a regional gold-bearing, intrusion-related, metallogenic event in eastern Alaska and central Yukon. This temporal link between Carlin-type mineralization and other mineralization types bears similarities with world-class sedimentary rock-hosted gold deposits of Nevada. This study demonstrates the potential of using LA-ICP-MS U-Pb dating on calcite to constrain the age of mineral deposits lacking synmineralization minerals amenable to classic dating techniques.

8 citations


Journal ArticleDOI
01 Feb 2022-Lithos
TL;DR: In this article , the authors presented new electron microprobe and laser-ablation inductively coupledplasma mass-spectrometry results for a suite of mantle xenoliths (n = 12) and olivine xenocrysts from the Jericho, Muskox, and Voyageur kimberlites (northern Slave craton, Canada).

5 citations


Journal ArticleDOI
17 Mar 2022
TL;DR: The trace element composition of detrital magnetite grains recovered from six local streams around the Casino high-grade porphyry Cu-Au-Mo deposit, west-central Yukon, is compared with igneous and magmatic-hydrothermal magnetite recovered from mineralized and unmineralized host rocks at the deposit as discussed by the authors .
Abstract: The trace element composition of detrital magnetite grains recovered from six local streams around the Casino high-grade porphyry Cu–Au–Mo deposit, west-central Yukon, is compared with igneous and magmatic-hydrothermal magnetite recovered from mineralized and unmineralized host rocks at the deposit. Linear discriminant analysis of 12 elements (Mg, Al, Ti, V, Mn, Co, Cr, Ni, Cu, Zn, Ga and Ge) and plots of Ti v. Ni/Cr are used to discriminate between magmatic-hydrothermal magnetite from the potassic alteration zone and igneous magnetite from granodiorite and quartz monzonite hosting the deposit. Magmatic-hydrothermal magnetite with a trace element composition similar to that from the potassic alteration zone at Casino is identifiable in stream sediments draining the deposit. Copper in magmatic-hydrothermal magnetite, present as minute inclusions of sulfide minerals such as chalcopyrite or substituted within the magnetite crystal lattice, is a strong indicator of Cu mineralization. We show that the chemical compositions of magnetite recovered from stream sediments can be used to explore for porphyry systems. Thematic collection: This article is part of the Applications of Innovations in Geochemical Data Analysis collection available at: https://www.lyellcollection.org/cc/applications-of-innovations-in-geochemical-data-analysis Supplementary material: Laser ablation data for major, minor and trace elements in magnetite from bedrock and stream sediment samples from Casino are available at https://doi.org/10.6084/m9.figshare.c.5896900

3 citations


Journal ArticleDOI
TL;DR: In this paper , an unsupervised machine learning approach was used to distinguish primary and late features in element maps and produce feature maps that depict textural relationships for comparison with the element maps.

2 citations


ReportDOI
01 Jan 2022
TL;DR: In this paper , the trace element variations in pyrite (Py) from Mississippi Valley type (MVT) and fracture-controlled replacement (FCR) deposits in the Kootenay Arc, British Columbia were investigated.
Abstract: This paper combines petrography with in situ laser-ablation inductively coupled plasma mass spectrometry to document trace-element variations in pyrite (Py) from Mississippi Valley-type (MVT) and fracture-controlled replacement (FCR) deposits in the Kootenay Arc, British Columbia. Three generations of pyrite are Py 1, Py 2, and Py 3. Pyrite 1, the earliest (occurring in MVT deposits only), has higher Ag, Ba, Cu, Ge, Pb, Sb, Sr, Tl, and V than adjacent Py 3. It has higher Ag, Au, Ba, Cu, Ge, Pb, and Tl than Py 2. Pyrite 2 occurs in MVT and FCR deposits. Relative to FCR Py 2, MVT Py 2 is enriched in Co, Ni, Mo, Ba, Tl, and Pb and depleted in other elements. The FCR Py 2 has growth-related compositional banding, which is absent in MVT Py 2. The FCR Py 2 has Ag, Cu, Ga, Ge, In, Sn, and Zn enriched cores, intermediate Au- and As-rich bands, and Co- and Ni-rich rims. Pyrite 3, the latest occurring pyrite, present in MVT and FCR deposits, is enriched in Co and Ni near overgrowths or infillings of sphalerite. Variations in composition of Py reflect mineralogy, characteristics of ore-forming fluids, and differences in physicochemical conditions between MVT and FCR deposits at the time of ore deposition.

1 citations


Journal ArticleDOI
08 Jun 2022-Minerals
TL;DR: In this paper , a laser ablation-inductively coupled plasma-mass spectrometry (LA-ICP-MS) mapping of barren sandstone distal to mineralized areas was performed.
Abstract: The Proterozoic Athabasca Basin hosts a large number of high-grade, large-tonnage unconformity-related uranium (U) deposits, many of which are also enriched in rare earth elements (REE). The basin also contains hydrothermal REE mineralization unassociated with U. Previous studies postulated that U and REE were derived from either the basin or the basement; however, the exact source of the metals remains ambiguous. This study provides evidence of U- and REE-rich fluids throughout the Athabasca Basin through laser ablation-inductively coupled plasma-mass spectrometry (LA-ICP-MS) mapping of barren sandstone distal to mineralized areas. The results indicate that elevated U and REE concentrations mainly occur in the matrix; there are strong positive correlations between U and REE, Th, P and Sr, and moderate positive correlations between U and Zr, Ba, Fe, Al, K and Ca, but the few spots with the highest U are unrelated to these elements. Quantitative evaluation of the element correlations, together with scanning electron microscopy-energy dispersive spectroscopy (SEM-EDS) analysis, suggests that most of the elevated U and REE are hosted in aluminum phosphate sulfate (APS) minerals rather than apatite and monazite. As the APS minerals are of diagenetic-hydrothermal origin, the results testify to the presence of U- and REE-rich fluids within the Athabasca Basin. The elevated Th/U ratio (~10) and REE pattern (strong heavy rare earth element (HREE) depletion) are consistent with a model in which large amounts of U and REE (especially HREE) were leached from the sandstone within the Athabasca Basin and contributed to U and REE mineralization near the unconformity between the sedimentary rocks in the basin and underlying basement rocks. This study demonstrates that LA-ICP-MS mapping can be effectively used to evaluate microscale distribution of elements and their mobility in sedimentary rocks to address mineralization related problems.

1 citations


Journal ArticleDOI
TL;DR: In this article , the metal content of 12 metals in 20 legal and 21 illegal cannabis vape liquids was analyzed by scanning electron microscopy, and laser ablation inductively coupled plasma mass spectrometry confirmed the presence of copper-, zinc-, lead-, and manganese-bearing particles.
Abstract: Cannabis vaping involves the vaporization of a cannabis vaping liquid or solid via a vaping accessory such as a vape pen constructed of various metals or other parts. An increasing number of reports advocate for expansion of the testing and regulation of metal contaminants in cannabis vape liquids beyond the metals typically tested such as arsenic, cadmium, mercury, and lead to reflect the possibility of consumers’ exposure to other metal contaminants. Metal contaminants may originate not only from the cannabis itself but also from the vape devices in which the cannabis vape liquid is packaged. However, metal analyses of cannabis vape liquids sampled from cannabis vaping devices are challenged by poor precision and reproducibility. Herein, we present data on the metal content of 12 metals in 20 legal and 21 illegal cannabis vape liquids. The lead mass fraction in several illegal samples reached up to 50 μg g–1. High levels of nickel (max 677 μg g–1) and zinc (max 426 μg g–1) were found in illegal samples, whereas the highest copper content (485 μg g–1) was measured in legal samples. Significant differences in metal mass fractions were observed in the legal cannabis vape liquid taken from two identical devices, even though the liquid was from the same lot of the same cannabis product. Metal particles in the vape liquids were observed by scanning electron microscopy, and laser ablation inductively coupled plasma mass spectrometry confirmed the presence of copper-, zinc-, lead-, and manganese-bearing particles, metals that are in common alloys that may be used to make vape devices. Colocalized particles containing aluminum, silica, and sodium were also detected. These results suggest that metal particles could be a contributing factor to poor measurement precision and for the first time, to the best of our knowledge, provide evidence of metal particles in cannabis vape liquids contained in unused cannabis vape pens.

Journal ArticleDOI
TL;DR: The Archean Horne 5 deposit as mentioned in this paper contains a total resource of 172.4 mt Au (5.6 Moz) from 112.7 mt of ore grading at 1.53 g/t Au.
Abstract: The Archean Horne 5 deposit, located in the Rouyn-Noranda district in the southern Abitibi greenstone belt, Canada, contains a total resource of 172.4 t Au (5.6 Moz) from 112.7 Mt of ore grading at 1.53 g/t Au. The deposit is part of the Au-rich Horne volcanogenic massive sulfide (VMS) complex that also includes the past-producing Horne mine (i.e., the Upper and Lower H zones plus small subsidiary lenses) that yielded 325.4 t Au (10.5 Moz Au) from 53.7 Mt of ore grading at 6.06 g/t Au. Combined, the Horne mine and Horne 5 deposit contain ~500 t Au (16 Moz), making them the world’s single largest accumulation of VMS-related Au. The Horne 5 deposit consists of stacked lenses of massive to semimassive sulfides alternating with extensive zones of disseminated and stringer sulfides. The mineralization is hosted within thick accumulations of steeply dipping dacitic to rhyodacitic volcaniclastic units of transitional to calc-alkaline magmatic affinity. Dacitic-rhyodacitic synvolcanic units (lobes, sills, and/or domes) intrude the host succession, which is also crosscut by a series of post-ore mafic and younger intermediate to felsic feldspar ± quartz porphyry dikes. A broad and diffuse halo of distal sericite-chlorite-epidote alteration extends outboard of intensely sericite-altered zones proximal to the sulfide lenses. Gold is interpreted to be synvolcanic on the basis of Au-rich massive sulfide clasts in the volcaniclastic units, the presence of preserved Au-rich primary pyrite, Au zones limited to the sulfide envelope, crosscutting deformed but unaltered and barren dikes, and the absence of typical syndeformation, orogenic-style alteration and mineralization despite overprinting high-strain corridors and faults. Gold is spatially associated with pyrite, sphalerite, and chalcopyrite, and its distribution is largely controlled by the higher porosity and permeability of the volcaniclastic host rocks, which are interpreted to have facilitated hydrothermal fluid circulation in the subseafloor environment. Synvolcanic intrusions and fine-grained tuffs overlying auriferous zones also influenced the distribution of the mineralization by acting as cap rocks to ascending fluids. Evidence suggests that Au enrichment at the Horne 5 deposit is due to efficient transport and precipitation of Au in the subseafloor environment, a favorable geodynamic setting (transitional to calc-alkaline magmatism over thick crust), and possible input of magmatic fluids as suggested by high Te and Cu in the mineralization. Minor and very local remobilization of metals occurred in response to regional deformation and associated greenschist facies metamorphism. The detailed study of the Horne 5 deposit geology and a review of the available information on the Horne mine and recent 3-D modeling indicate that the Horne 5 deposit may have formed higher in the stratigraphy than the Upper and Lower H orebodies of the former Horne mine, which originally formed a single lens. Therefore, the Horne Au-rich VMS complex originally formed as a stacked system in which the Horne 5 deposit was deposited above the Upper and Lower H zones and not in a distal or lateral position as previously proposed, indicating that a robust hydrothermal system was responsible for the formation of the world’s largest Au-rich VMS complex.