Geology ReportsSearch

USGS · 70207998

Zircon-hosted melt inclusion record of silicic magmatism in the Mesoproterozoic St. Francois Mountains terrane, Missouri: Origin of the Pea Ridge iron oxide-apatite rare earth element deposit and implications for regional crustal pathways of mineralization

Abstract

Voluminous silicic magmatism was coeval with iron ore mineralization in the St. Francois Mountains terrane in southeast Missouri, part of the broader Mesoproterozoic Granite-Rhyolite province along the eastern margin of Laurentia. Some of the iron deposits contain extraordinary endowments of critical elements, such as the Pea Ridge iron oxide-apatite (IOA) deposit, which has an average grade of ~12 wt% rare earth oxides in breccia pipes that flank the ore body. To assess the role of silicic magmatism in the genesis of the Pea Ridge deposit, we present a high-spatial resolution study of zirconhosted melt inclusions from rhyolitic ash-flow tuffs. Melt inclusion data are combined with textural, geochemical, and geochronological analyses of zircon hosts to elucidate the magmatic-hydrothermal evolution of the Pea Ridge system. Two contemporaneous silicic igneous centers in the St. Francois Mountains terrane, Bourbon and Eminence, were studied for comparison. Pea Ridge melt inclusions are trachydacitic to rhyolitic (~63-79 wt% SiO2, ~5.6-11.7 wt% Na2O+K2O) with very high Cl in the least-evolved and most alkaline melt inclusions (~2,000-5,000 ppm Cl). Rare earth elements (REE) in melt inclusions have identical chondrite-normalized patterns to the mineralized breccia pipes, but with systematically lower absolute concentrations. Haplogranite ternary pressures range from ~0.5-10 kbar, with an average of ~2-3 kbar (7-12 km depth), and liquidus temperatures are ~850-950 °C, with an average of ~920 °C. Silicate and phosphate mineral inclusions have compositions that overlap minerals from the iron ore body and breccia pipes, recording a transition from igneous to hydrothermal zircon growth. Igneous iron oxide inclusions have compositions that indicate Pea Ridge magmas were reduced to moderately oxidized (log fO2 of -0.8 to -1.84 NNO). Zircons from two Pea Ridge samples have 207Pb/206Pb concordia ages of 1456 ± 9 Ma and 1467 ± 13 Ma that overlap published ages for the breccia pipes and iron ore zones of the Pea Ridge deposit. A population of texturally and chemically disrupted zircons have discordant domains that correspond to high Fe, U, and REE concentrations, consistent with the unique geochemical attributes of the IOA-REE ore body. Inherited cores in Pea Ridge and Bourbon zircons have concordant 207Pb/206Pb dates of 1550-1618 Ma, providing direct evidence of cratonic basement beneath these centers. Oxygen isotope data for inherited and autocrystic igneous zircons span from mantle to crustal values (18Ozircon=5.5-7.9‰). Our data are consistent with a model in which metasomatized mantle components were mixed with cratonic and accreted crustal material in a back-arc or rifted segment of a volcanic arc, with ore fluids derived from Cl-rich melts to transport Fe and REE in a long-lived (tens of Myr), pulsed, magmatic-hydrothermal system. Bourbon, which also possesses IOA mineralization, shares key petrologic similarities with the Pea Ridge system, whereas Eminence, which is not mineralized, has disparate geochemical and isotopic signatures that indicate it formed in a different crustal setting. The location of Pea Ridge and Bourbon along a cratonic margin may have been important in focusing silicic melts and mineralization in the upper crust, serving as a guide for future exploration efforts.

Explore related subjects

90° N90° S · 180° W ← longitude → 180° E
Source-reported bounding extent: 36.58024660149866° to 38.34165619279595° latitude; -92.2412109375° to -89.967041015625° longitude. This indicates report coverage, not an exact sampling location. View area on OpenStreetMap.

Keep this discovery

Explore connections, maps & timelines

BibTeXRIS

Kathryn E. Watts, Celestine N. Mercer. 2020. Zircon-hosted melt inclusion record of silicic magmatism in the Mesoproterozoic St. Francois Mountains terrane, Missouri: Origin of the Pea Ridge iron oxide-apatite rare earth element deposit and implications for regional crustal pathways of mineralization. https://doi.org/10.1016/j.gca.2019.12.032

Cite the original work for its findings. Save a collection to share your selection of sources.

KEEP EXPLORING

Related USGS reports

Organic and isotopic indicators for sorting of sedimentary organic matter along a marginal submarine canyon

Submarine canyons are incised features of many continental margins that can have significant influence on the hydrodynamic distribution of sediments and organic matter eroded and deposited from the continents. Baltimore Canyon, on the mid-Atlantic margin of the United States, contains a complex set of sedimentary processes that simultaneously create unique benthic habitats and control the deposition of organic matter. Along the canyon axis, loci of net erosion, net deposition, and intense winnowing each host diverse faunal assemblages and varying mixtures of sedimentary organic matter derived both from production in the overlying water column and from mobilized sediments. Bioavailable components of this deposited organic matter sustain benthic communities, while recalcitrant components can contribute to long-term carbon burial in the deep sea. However, commonly employed bulk geochemical analyses provide little information about the relative bioavailability or depositional history of sedimentary organic matter. Here we employ a range of organic and isotopic analyses to explore in more detail how canyon-specific sediment dynamics determine the sorting of organic matter from shelf to open ocean. In combination with bulk geochemical characteristics, we subjected surface sediments from water depths of ∼200–1200 m in Baltimore Canyon to a sequential extraction procedure, isolating nonpolar and polar lipid classes, an acid-soluble fraction, and an acid-insoluble fraction. Each class was analyzed for carbon and nitrogen quantities and stable isotope ratios, and radiocarbon content where possible, along with compound-specific carbon and nitrogen isotope analysis of individual amino acids in the acid-hydrolysed fraction. We find different organic matter sources and depositional history recorded in the properties of younger, bioavailable organic matter components (polar lipids, amino acids) in comparison to the older, more recalcitrant components (nonpolar lipids, acid-insoluble fraction). These differences in source and bioavailability of organic matter vary along the canyon, correlating with grain size and erosion/deposition dynamics, and may help shape the benthic faunal assemblages. Additionally, our results suggest that determining the relative concentrations of acid-soluble and acid-insoluble organic matter may provide an easily accessible method to improve our understanding of the nutritional quality of sediments for benthic fauna than more commonly used bulk carbon or nitrogen concentrations.

Delaware, New Jersey

Bayesian calibration of the 40K decay scheme with implications for 40K-based geochronology

The K/Ar and 40 Ar/ 39 Ar geochronometers are based on the naturally occurring radionuclide 40 K. Their precision and accuracy are limited by uncertainties on the 40 K decay constants and, in the case of the 40 Ar/ 39 Ar geochronometer, the isotopic composition of neutron fluence monitors. To address these limitations, we introduce a Bayesian calibration of the 40 K decay scheme. We formulate robust priors for all model parameters including partial 40 K decay constants, 238 U and 235 U decay constants, and age offset parameters to account for phenomena that can perturb apparent U-Pb and 40 Ar/ 39 Ar ages. We then harness a set of complementary 40 Ar/ 39 Ar, 238 U/ 206 Pb, and 235 U/ 207 Pb data from well- characterized geological samples with ages from 1.919 ka to 2000 Ma to derive Bayesian estimates of the 40 K decay constants. Posterior values for the partial 40 K decay constants are λ β - "> λ β - = (4.9252 ± "> ± 0.0054) × "> × 10 −10 yr −1 , λ β + "> λ β + = (5.6658 ± "> ± 0.1543) × "> × 10 −15 yr −1 , λ EC ∗ "> λ EC0 = (5.7404 ± "> ± 0.0053) × "> × 10 −11 yr −1 , and λ EC 0 "> λ EC0 = (4.9060 ± "> ± 0.2942) × "> × 10 −13 yr −1 (uncertainties reported at the 68 % (1 σ "> σ ) credible interval). These combine to a total 40 K decay constant λ tot "> λ tot = (5.5042 ± "> ± 0.0054) × "> × 10 −10 yr −1 . Model estimates of the 238 U and 235 U decay constants are statistically indistinguishable from those reported by Jaffey et al. (1971) . Posterior values of the 40 K decay constants and the 40 Ar*/ 40 K isotopic composition of Fish Canyon sanidine (FCs) define a K/Ar FCs age of 28.183 ± "> ± 0.017 Ma (1 σ "> σ ). Significantly, Bayesian calibrated 40 Ar/ 39 Ar ages align with astronomically tuned ages throughout the Cenozoic and with 238 U/ 206 Pb and 235 U/ 207 Pb ages in the Mesozoic, Paleozoic, and Proterozoic, as well as having comparable precision to the 238 U/ 206 Pb method. Thus, Bayesian calibration of the 40 K decay scheme and the K/Ar age of FCs reconciles the 40 Ar/ 39 Ar, U-Pb, and astronomical chronometers.

Geochimica et Cosmochimica Acta

Characterizing sulfur redox state and geochemical implications in deep-time using mineral chemistry network analysis

Sulfur (S) is a central element in global biogeochemical cycling and Earth’s redox evolution. Minerals that contain S are an important record of local environmental conditions at the time of their formation based on chemical speciation and redox. However, the oxidation state of S for hundreds of different S-containing minerals and thousands of S-containing mineral localities is unknown, largely sulfides and sulfosalts, and the redox state alone does not fully capture mineral chemistry diversity, thus limiting understanding of S redox evolution. Here, we use mineral chemistry network analysis and the weighted Mineral Element Electronegativity Coefficient of Variation (wMEE CV ) metric to investigate the element interactions and localities of S-containing minerals from the Mineral Evolution Database (MED) to infer the redox state of S in minerals where the redox state is unknown (S U ). Louvain community detection of the S mineral chemistry redox network reveals that there are three main network communities that are separated by redox state. The S 6+ community includes minerals that contain the S 6+ redox state and a small number of S 4+ and S 2+ minerals, the S 2− community includes S 2− -containing minerals, and the S U community includes minerals in which the redox state of S is unknown. The wMEE CV values of the S U community closely overlap with the wMEE CV values of the S 2− community, and do not overlap with the wMEE CV values of the S 6+ community, indicating the S U community minerals contain predominately reduced S. Assuming that S U community minerals contain reduced S, as supported by their network chemical associations and wMEE CV values, then reduced S-containing minerals make up approximately 81 % of S-containing mineral localities in the S mineral chemistry network, even though the majority of all mineral localities (S-containing and non-S-containing) are oxygen (O)-containing minerals. Additionally, reduced S-containing minerals make up the majority (∼75 %) of all non-O containing mineral localities in the MED, representing the importance of reduced S as an electron source and substrate in the evolution of microbial metabolic networks. The range wMEE CV values of S 6+ community minerals expands through time due primarily to formation of chemically diverse sulfate minerals, coinciding with crustal oxidation from the late Proterozoic to Phanerozoic and the expansion of the marine sulfate reservoir. The intersection of shared constituent elements among reduced and oxidized S in the mineral chemistry network represents redox convergence of weathered S in the geosphere that was crucial in the formation of natural resource deposits and the evolution of biogeochemical cycles.

Geochimica et Cosmochimica Acta