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Research about Yellowstone Plateau Volcanic Field

Source-linked reports with geographic coverage including Yellowstone Plateau Volcanic Field.

4 recordsLinked to original sources

Radiogenic strontium- and uranium-isotope tracers of water-rock interactions and hydrothermal flow in the Upper Geyser Basin, Yellowstone Plateau Volcanic Field, USA

Natural radiogenic isotopes (primarily 87 Sr/ 86 Sr) from hot springs in the Upper Geyser Basin of the Yellowstone Plateau volcanic field and associated rocks were used to evaluate groundwater flow patterns, water-rock reactions, and the extent of mixing between various groundwater sources. Thermal waters have very low uranium concentrations and 234 U/ 238 U activity ratios near 1.0, which limit their utility as tracers in this reducing setting. Thermal waters have higher Sr concentrations (<22 ng/g) and a wide range of 87 Sr/ 86 Sr values that vary both temporally at individual discharge sites and between adjacent springs, indicating that conduits tap different subsurface reservoirs to varying degrees. Sr from local rhyolites have 87 Sr/ 86 Sr compositions that bound the range of values observed in groundwater throughout the basin. Non-boiling springs on the west flank of the basin discharge water with low 87 Sr/ 86 Sr consistent with flow through young volcanic rocks exposed at the surface. Boiling springs in the central basin have higher 87 Sr/ 86 Sr values reflecting interactions with older, more radiogenic volcanic rocks. Variability in upwelling thermal waters requires mixing with a low 87 Sr/ 86 Sr component derived from young lava or glacial sediments, or more likely, from deeper sources of hot groundwater circulating through buried Lava Creek Tuff having intermediate 87 Sr/ 86 Sr. Isotope data constrain basin-wide output of thermal water to 110–140 kg·s −1 . Results underscore the utility of radiogenic Sr isotopes as valuable tracers of hydrothermal flow patterns and improve the understanding of temperature-dependent water-rock reactions in one of the largest continental hydrothermal systems on Earth.

Wyoming↗

The source, fate, and transport of arsenic in the Yellowstone hydrothermal system - An overview

The Yellowstone Plateau Volcanic Field (YPVF) contains >10,000 thermal features including hot springs, pools, geysers, mud pots, and fumaroles with diverse chemical compositions. Arsenic (As) concentrations in YPVF thermal waters typically range from 0.005 to 4 mg/L, but an As concentration of 17 mg/L has been reported. Arsenic data from thermal springs, outflow drainages, rivers, and from volcanic rocks and silica sinter were used to identify the sources, characterize geochemical and microbial processes affecting As, and quantify As fluvial transport. Arsenic in YPVF thermal waters is mainly derived from high temperature leaching of rhyolites. Arsenic concentrations in thermal waters primarily depend on water type, which is controlled by boiling, evaporation, mixing, and mineral precipitation and dissolution. Springs with low As concentrations include acid-SO 4 (0.1 ± 0.1 mg/L), NH 4 -SO 4 rich (0.003 ± 0.007 mg/L), and dilute thermal waters (0.1 ± 0.1 mg/L); travertine-forming waters have moderate As concentrations (0.4 ± 0.2 mg/L); and neutral- Cl waters (1.2 ± 0.8 mg/L) common in the western portion of the Yellowstone Caldera and Cl-rich waters (1.9 ± 1.2 mg/L) primarily from Basins near the Caldera boundary have elevated As concentrations. Reduced As species (arsenite and thiolated-As species) are most prevalent near the orifice of hot springs, and then As rapidly oxidizes to arsenate along drainages. Previously published cultivation-based studies and metagenomic data from microbial communities inhabiting a variety of hot springs indicate a widespread distribution of arsenite oxidation and arsenate reduction capabilities among the hot springs. Widespread use and transformation of As by thermophilic microorganisms promotes more soluble and toxic forms. Most of the water discharged from thermal springs eventually ends up in a nearby river where As remains soluble and exhibits little attenuation during downstream transport. Since 2010, 183 ± 10 metric tons/year of As were transported from Yellowstone National Park (YNP) via rivers. The discharge from YPVF thermal features impairs river water quality whereby As concentrations exceed 10 μg/L for many rivers reaches within and downstream from YNP.

Idaho, Montana, Wyoming↗

Quantifying non-thermal silicate weathering using Ge/Si and Si isotopes in rivers draining the Yellowstone Plateau Volcanic Field, USA

In active volcanic regions, high-temperature chemical reactions in the hydrothermal system consume CO 2 sourced from magma or from the deep crust, whereas reactions with silicates at shallow depths mainly consume atmospheric CO 2 . Numerous studies have quantified the load of dissolved solids in rivers that drain volcanic regions to determine chemical weathering rates and atmospheric CO 2 consumption rates. However, the balance between thermal and non-thermal components to riverine fluxes in these areas remains poorly constrained, hindering accurate estimates of atmospheric CO 2 consumption rates. Here we use the Ge/Si ratio and the stable silicon isotopes (δ 30 Si) as tracers for quantifying non-thermal silicon contributions in rivers draining the Yellowstone Plateau Volcanic Field, USA. The Ge/Si ratio (µmol.mol −1 ) was determined for seven thermal water samples (183 ± 22), eight rivers (35 ± 23) and six creeks flowing into Yellowstone Lake (5 ± 3) during base flow and during peak water discharge following snowmelt. The δ 30 Si value (‰) was determined for thermal waters (−0.09 ± 0.04), Yellowstone River at Yellowstone Lake outlet (1.91 ± 0.23) and creek samples (0.82 ± 0.29). The calculated atmospheric CO 2 consumption associated with non-thermal waters flowing through Yellowstone's rivers during peak discharge is ∼3.03 ton.km −2 .yr −1 , which is ∼2% of the annual mean atmospheric CO 2 consumption in other volcanic regions. This study highlights the significance of quantifying seasonal variations in chemical weathering rates for improving estimates of atmospheric CO 2 consumption rates in active volcanic regions.

Wyoming↗

The systematics of chlorine, lithium, and boron and δ37Cl, δ7Li, and δ11B in the hydrothermal system of the Yellowstone Plateau Volcanic Field

Chlorine, lithium, and boron are trace elements in rhyolite but are enriched in groundwater flowing through rhyolite because they tend to partition into the fluid phase during high‐temperature fluid‐rock reactions. We present a large data set of major element and δ 37 Cl, δ 7 Li, and δ 11 B compositions of thermal water and rhyolite from Yellowstone Plateau Volcanic Field (YPVF). The Cl/B, Cl/Li, δ 37 Cl (−0.2‰ to +0.7‰), and δ 11 B (−6.2‰ to −5.9‰) values of alkaline‐chloride thermal waters reflect high‐temperature leaching of chlorine, lithium, and boron from rhyolite that has δ 37 Cl and δ 11 B values of +0.1‰ to +0.9‰ and −6.3‰ to −6.2‰, respectively. Chlorine and boron are not reactive, but lithium incorporation into hydrothermal alteration minerals result​s in a large range of Cl/Li, B/Li, and δ 7 Li (−1.2‰ to +3.8‰) values in thermal waters. The relatively large range in δ 7 Li values of thermal waters reflects a large range of values in rhyolite. Large volumes of rhyolite must be leached to account for the chloride, lithium and boron fluxes, implying deep groundwater flow through rhyolite flows and tuffs representing Yellowstone's three eruptive cycles (∼2.1 Ma). Lower Cl/B values in acid‐sulfate waters result from preferential partitioning of boron into the vapor phase and enrichment in the near‐surface water condensate. The Cl/B, Cl/Li, δ 7 Li (−0.3‰ to +2.1‰), and δ 11 B (−8.0‰ to −8.1‰) values of travertine depositing calcium‐carbonate thermal waters which discharge in the northern and southern YPVF suggest that chlorine, lithium, and boron are derived from Mesozoic siliciclastic sediments which contain detrital material from the underlying metamorphic basement.

Wyoming↗