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Corey J. Meighan

Publications and source records attributed to Corey J. Meighan.

8 recordsLinked to original sources

Geochemistry and thermometry of magnetite veins and replacements in iron ore deposits from the Iron Springs district, SW Utah, USA: Relation to magmatic and hydrothermal processes

Ore-genesis, texture, chemical compositions, and thermometry of magnetite were used to better evaluate the origins of iron ore deposits across the Iron Spring district, Utah. Trace element compositions, determined by LA-ICP-MS, were used to calculate temperatures based on X Mg numbers and characterize the trace element signatures of magmatic and hydrothermal magnetite. Magnetite occurs as coarser crystalline grains within veins, breccias, and cavities along with finer crystalline replacements. Magnetite is most commonly intergrown with apatite, phlogopite, and carbonate in veins, breccias, and cavities where apatite occurs separately from the other gangue minerals. The results using empirical trace element discrimination diagrams generally suggest that the magnetite is overall of hydrothermal origin regardless of textural variations or field relationships. The X Mg numbers of the magnetite in the magnetite-apatite ores, however, are suggestive of high temperature magmatic conditions; whereas those of vein, breccia, and replacement occurrences containing other gangue minerals are suggestive of lower temperature hydrothermal processes.

Utah↗

Critical mineral inventory of select IOA-IOCG deposits, southwestern USA

Critical minerals are necessary for modern technology and strategic purposes. Their increasing importance requires finding new and nontraditional resources. Samples of ore, altered, and unaltered host rock were collected from 26 iron mines and prospects in California, Nevada, and Utah to assess the potential of these deposits to host economic quantities of different critical minerals. Geochemical analyses were conducted by 61 element ICP-OES-MS sodium peroxide fusion and major elements determined by WDXRF. These deposits concentrated many critical minerals beyond what is found in average upper crustal abundances, such as Sb, As, Bi, Co, Ga, Mg, Mn, Ni, Nb, Pd, REE, Sc, Te, Sn, Ti, W, V, and Zn. However, most of these are not concentrated enough in the ore to be considered as economic resources. Those critical minerals that are enriched enough in some of these deposits to possibly be considered as by-product commodities are Ni, REE, V, and potentially Co and Ga. These enrichments were not uniform, with REE more likely to be enriched in IOA deposits, whereas Co, Ga, Ni, and V could be found enriched in either IOA or IOCG deposits.

California, Nevada, Utah↗

Geochemistry of hematite veins in IOA-IOCG deposits of SE Missouri, USA: Relation to felsic magmatism and caldera lakes

The paragenesis, textures, and chemical compositions of secondary hematite in regional potassic altered rhyolites, four IOA deposits, the sedimentary iron deposit at Pilot Knob and the Boss IOCG deposit in SE Missouri were determined and compared to primary magnetite from the IOA and IOCG deposits. Magnetite is composed of elements characteristics of mafic to intermediate intrusions whereas hematite is enriched in elements characteristic of felsic igneous rocks. These results suggest that magnetite formed from fluids discharged from mafic to intermediate composition intrusions. Hematite precipitated from fluids discharged from felsic intrusions or fluids that evolved in caldera lakes. Hematite in the sedimentary iron deposit at Pilot Knob formed in an evaporative caldera lake with fluid inputs from felsic intrusions.

Missouri↗

Absence of magnetite microlites, geochemistry of magnetite veins and replacements in IOA deposits, SE Missouri, USA: Relations to intermediate intrusions

The paragenesis, textures, and chemical compositions of magnetite in two mafic to intermediate intrusions and four IOA deposits in SE Missouri were studied to discriminate between igneous and hydrothermal sources. In this study, we found that replacement magnetite with mineral inclusion-rich cores yields erroneously high Ti, Al, Si, Mg, and Mn contents as determined by EMP and LA-ICP-MS due to rutile and silicate inclusions. Thus, identification of high-Ti microlites on the basis of inclusion-rich cores with high Ti contents is an analytical artefact. Since the high-Ti magnetite microlite flotation model is critically dependent on this type of analysis, it may be invalid. The presence of coarse-grained high-Ti vein magnetite with ilmenite lamellae enveloped by replacement magnetite with inclusion-rich cores in ore zones suggests that the veins were high-temperature conduits for low-temperature replacement ores. The trace element compositions of vein and replacement magnetite suggest that iron was sourced from mafic to intermediate intrusions. These results support a magmatic-hydrothermal origin for IOA systems in SE Missouri.

Missouri↗

Compilation of new and previously published geochemical and modal data for Mesoproterozoic igneous rocks of the St. Francois Mountains, southeast Missouri

The purpose of this report is to present recently acquired as well as previously published geochemical and modal petrographic data for igneous rocks in the St. Francois Mountains, southeast Missouri, as part of an ongoing effort to understand the regional geology and ore deposits of the Mesoproterozoic basement rocks of southeast Missouri, USA. The report includes geochemical data that is (1) newly acquired by the U.S. Geological Survey and (2) compiled from numerous sources published during the last fifty-five years. These data are required for ongoing petrogenetic investigations of these rocks. Voluminous Mesoproterozoic igneous rocks in the St. Francois Mountains of southeast Missouri constitute the basement buried beneath Paleozoic sedimentary rock that is over 600 meters thick in places. The Mesoproterozoic rocks of southeast Missouri represent a significant component of approximately 1.4 billion-year-old (Ga) igneous rocks that crop out extensively in North America along the southeast margin of Laurentia and subsequent researchers suggested that iron oxide-copper deposits in the St. Francois Mountains are genetically associated with ca. 1.4 Ga magmatism in this region. The geochemical and modal data sets described herein were compiled to support investigations concerning the tectonic setting and petrologic processes responsible for the associated magmatism.

Missouri↗

Mineralogy, chemistry, and fluid-aided evolution of the Pea Ridge Fe oxide-(Y + REE) deposit, southeast Missouri, USA

The Kiruna-type Pea Ridge iron oxide-apatite (IOA) deposit is hosted by a sequence of 1.47 Ga rhyolite tuffs of the St. Francois Mountains, southeast Missouri, USA. It consists of a series of altered zones composed mainly of amphibole, magnetite, hematite, and quartz, together with the presence of several rare earth element (Y + REE)-rich breccia pipes. In many cases, the fluorapatite within these zones is rich in inclusions of monazite, iron oxide, and quartz inclusions, plus minor xenotime. Monazite and minor xenotime are also found intergrown as inclusions in the fluorapatite, as well as in surrounding recrystallized magnetite and hematite in the magnetite ore. Monazite and xenotime typically occur as inclusions within both oxides. Monazite-(Ce) and xenotime-(Y) are both relatively poor (<2 wt %) in ThO 2 and UO 2 . No significant compositional differences exist in the (Y + REE) chemistry between monazite and xenotime inclusions in fluorapatite compared to grains intergrown with magnetite and hematite, suggesting that these two REE-rich minerals are cogenetic. Monazite-xenotime geothermometry and geochronology of monazite inclusions in fluorapatite provide evidence that formation/remobilization of the (Y + REE) phosphates took place at ca. 50° to 400°C, approximately 5 to 10 m.y. after emplacement of the main iron oxide-phosphate orebody. Evidence from field relationships and fluid inclusion chemistry, together with the massive recrystallization and remobilization of fluorapatite, monazite, xenotime, and iron oxides at Pea Ridge, suggest a subvolcanic origin coupled with a strong metasomatic reworking of the IOA deposit.

Missouri↗

Mineral thermometry and fluid inclusion studies of the Pea Ridge iron oxide-apatite–rare earth element deposit, Mesoproterozoic St. Francois Mountains Terrane, southeast Missouri, USA

Mineral thermometry and fluid inclusion studies were conducted on variably altered and mineralized samples from the Mesoproterozoic Pea Ridge iron oxide-apatite (IOA)-rare earth element (REE) deposit in order to constrain P-T conditions, fluid chemistry, and the source of salt and volatiles during early magnetite and later REE mineralization. Scanning electron microscopy (SEM)-cathodoluminescence and SEM-backscatter electron images show that quartz and rutile precipitated before, during, and after magnetite and REE mineral growth. Ti-in-quartz and Zr-in-rutile equilibration temperatures range from ≤350° to 750°C in the amphibole, magnetite, hematite, and silicified zones where T increased during magnetite and quartz growth and dropped precipitously after fracturing and brecciation. Late drusy quartz cements within a REE-rich breccia pipe record the lowest T (≤315°–400°C). Liquid-, vapor-rich, and hypersaline (±hematite, calcite) fluid inclusions are common and liquid CO 2 is present locally. Salinities define three populations: saline (10–27 wt % NaCl equiv), hypersaline (34–>60 wt % NaCl equiv), and dilute (0–10 wt % NaCl equiv ). The wide range of eutectic melting temperatures (−67° to −19°C) suggests that saline inclusions trapped variable proportions of a CaCl-MgCl-FeCl-bearing fluid end member and an NaCl-KCl fluid end member. Homogenization temperatures and pressures of these saline inclusions suggest they were trapped when fluids unmixed into brine and vapor at T <350°C, P <15 MPa, and a depth of ~1.5 km. Hypersaline inclusions were trapped at low T and P (~200°C and ~1 MPa) along the V + L + H curve when the system vented to the paleosurface. Data for dilute inclusions in late drusy quartz from the REE-rich breccia pipe are indicative of a boiling epithermal environment. The Na/Cl, Na/K, and Cl/Br ratios of fluid inclusion extracts provide evidence for mixtures of magmatic hydrothermal fluids and evaporated seawater. Extracts from magnetite, hematite, and pyrite plot in the magmatic-hydrothermal field, indicating that Fe was derived from a magmatic source. Their enrichments in Mg and Ca are consistent with a mafic magmatic source. The positive correlation between Na/Mg and Na/Ca ratios may be due to halite saturation or albitization of igneous rocks. Extracts from barite in the REE-rich breccia pipes are enriched in Na and Br and plot near the seawater evaporation trend. He is highly enriched relative to Ne and Ar in fluid inclusion extracts, which precludes air as a source of He. Although the He is mostly of crustal origin, pyrite with a 3 He/ 4 He (R/R A ) of 0.1 contains up to 12% mantle He. Many extracts have low 20 Ne/ 22 Ne ratios due to nucleogenic production of 22 Ne in high F/O minerals such as fluorapatite or F biotite. The arrays of data for 3 He/ 4 He (R/R A ) and 22 Ne/ 20 Ne suggest that volatiles were derived from two sources, a moderate F mafic magma containing mantle He and a high F silicic magma with crustal He. Together with other evidence cited in this report, these data (1) support a magmatic hydrothermal origin for the Mesoproterozoic magnetite-apatite deposit with ore fluids derived from a concealed mafic to intermediate-composition intrusion, (2) suggest that the REE minerals in breccia pipes were either derived from apatite or precipitated in response to decompression and cooling during breccia pipe formation, (3) provide evidence for the influx of basinal brine, magmatic fluids from granitic intrusions, and meteoric water after breccia pipe formation, and (4) show that Pea Ridge was relatively unaffected by the late Paleozoic Mississippi Valley-type (MVT) Pb-Zn system in overlying Cambrian sedimentary rocks.

Missouri↗

Mineral deposits and metallogeny of Alaska

Alaska, the largest State within the United States, and mainly located north of latitude 60°, is an important part of the Circum-Arctic region. Alaska is a richly endowed region with a long and complex geologic history. The mining history is short by world standards but nevertheless there are a number of world-class deposits in Alaska, of which Red Dog and Pebble are among the largest of their respective types in the world. Alaska is a collection of geologic terranes or regions having distinct histories, most of which were tectonically assembled in the period from 400 million years to 50 million years ago (late Paleozoic through early Tertiary). They now occur as numerous fault-bounded blocks in the northernmost part of the North American Cordillera on the western margin of the Laurentian craton. These terranes are comprised of rocks ranging in age from Paleoproterozoic to Recent.

Alaska↗