Geology topics

Andrew G. Hunt

Publications and source records attributed to Andrew G. Hunt.

At least 55 records · Page 3Linked to original sources

USGS2016

Helium as a tracer for fluids released from Juan de Fuca lithosphere beneath the Cascadia forearc

The ratio between helium isotopes (3He/4He) provides an excellent geochemical tracer for investigating the sources of fluids sampled at the Earth's surface. 3He/4He values observed in 25 mineral springs and wells above the Cascadia forearc document a significant component of mantle-derived helium above Juan de Fuca lithosphere, as well as variability in 3He enrichment across the forearc. Sample sites arcward of the forearc mantle corner (FMC) generally yield significantly higher ratios (1.2-4.0 RA) than those seaward of the corner (0.03-0.7 RA). The highest ratios in the Cascadia forearc coincide with slab depths (40-45 km) where metamorphic dehydration of young oceanic lithosphere is expected to release significant fluid and where tectonic tremor occurs, whereas little fluid is expected to be released from the slab depths (25-30 km) beneath sites seaward of the corner.Tremor (considered a marker for high fluid pressure) and high RA values in the forearc are spatially correlated. The Cascadia tremor band is centered on its FMC, and we tentatively postulate that hydrated forearc mantle beneath Cascadia deflects a significant portion of slab-derived fluids updip along the subduction interface, to vent in the vicinity of its corner. Furthermore, high RA values within the tremor band just arcward of the FMC, suggest that the innermost mantle wedge is relatively permeable.Conceptual models require: (1) a deep fluid source as a medium to transport primordial 3He; (2) conduits through the lithosphere which serve to speed fluid ascent to the surface before significant dilution from radiogenic 4He can occur; and (3) near lithostatic fluid pressure to keep conduits open. Our spatial correlation between high RA values and tectonic tremor provides independent evidence that tremor is associated with deep fluids, and it further suggests that high pore pressures associated with tremor may serve to keep fractures open for 3He migration through ductile upper mantle and lower crust.

Geochemistry International↗

USGS2016

Groundwater ages from the freshwater zone of the Edwards aquifer, Uvalde County, Texas—Insights into groundwater flow and recharge

Tritium–helium-3 groundwater ages of the Edwards aquifer in south-central Texas were determined as part of a long-term study of groundwater flow and recharge in the Edwards and Trinity aquifers. These ages help to define groundwater residence times and to provide constraints for calibration of groundwater flow models. A suite of 17 samples from public and private supply wells within Uvalde County were collected for active and noble gases, and for tritium–helium-3 analyses from the confined and unconfined parts of the Edwards aquifer. Samples were collected from monitoring wells at discrete depths in open boreholes as well as from integrated pumped well-head samples. The data indicate a fairly uniform groundwater flow system within an otherwise structurally complex geologic environment comprised of regionally and locally faulted rock units, igneous intrusions, and karst features within carbonate rocks. Apparent ages show moderate, downward average, linear velocities in the Uvalde area with increasing age to the east along a regional groundwater flow path. Though the apparent age data show a fairly consistent distribution across the study area, many apparent ages indicate mixing of both modern (less than 60 years) and premodern (greater than 60 years) waters. This mixing is most evident along the “bad water” line, an arbitrary delineation of 1,000 milligrams per liter dissolved solids that separates the freshwater zone of the Edwards aquifer from the downdip saline water zone. Mixing of modern and premodern waters also is indicated within the unconfined zone of the aquifer by high excess helium concentrations in young waters. Excess helium anomalies in the unconfined aquifer are consistent with possible subsurface discharge of premodern groundwater from the underlying Trinity aquifer into the younger groundwater of the Edwards aquifer.

Texas↗

USGS2016

Dissolved gases in hydrothermal (phreatic) and geyser eruptions at Yellowstone National Park, USA

Multiphase and multicomponent fluid flow in the shallow continental crust plays a significant role in a variety of processes over a broad range of temperatures and pressures. The presence of dissolved gases in aqueous fluids reduces the liquid stability field toward lower temperatures and enhances the explosivity potential with respect to pure water. Therefore, in areas where magma is actively degassing into a hydrothermal system, gas-rich aqueous fluids can exert a major control on geothermal energy production, can be propellants in hazardous hydrothermal (phreatic) eruptions, and can modulate the dynamics of geyser eruptions. We collected pressurized samples of thermal water that preserved dissolved gases in conjunction with precise temperature measurements with depth in research well Y-7 (maximum depth of 70.1 m; casing to 31 m) and five thermal pools (maximum depth of 11.3 m) in the Upper Geyser Basin of Yellowstone National Park, USA. Based on the dissolved gas concentrations, we demonstrate that CO 2 mainly derived from magma and N 2 from air-saturated meteoric water reduce the near-surface saturation temperature, consistent with some previous observations in geyser conduits. Thermodynamic calculations suggest that the dissolved CO 2 and N 2 modulate the dynamics of geyser eruptions and are likely triggers of hydrothermal eruptions when recharged into shallow reservoirs at high concentrations. Therefore, monitoring changes in gas emission rate and composition in areas with neutral and alkaline chlorine thermal features could provide important information on the natural resources (geysers) and hazards (eruptions) in these areas.

Idaho, Montana, Wyoming↗

USGS2016

Determining CO 2 storage potential during miscible CO 2 enhanced oil recovery: Noble gas and stable isotope tracers

Rising atmospheric carbon dioxide (CO 2 ) concentrations are fueling anthropogenic climate change. Geologic sequestration of anthropogenic CO 2 in depleted oil reservoirs is one option for reducing CO 2 emissions to the atmosphere while enhancing oil recovery. In order to evaluate the feasibility of using enhanced oil recovery (EOR) sites in the United States for permanent CO 2 storage, an active multi-stage miscible CO 2 flooding project in the Permian Basin (North Ward Estes Field, near Wickett, Texas) was investigated. In addition, two major natural CO 2 reservoirs in the southeastern Paradox Basin (McElmo Dome and Doe Canyon) were also investigated as they provide CO 2 for EOR operations in the Permian Basin. Produced gas and water were collected from three different CO 2 flooding phases (with different start dates) within the North Ward Estes Field to evaluate possible CO 2 storage mechanisms and amounts of total CO 2 retention. McElmo Dome and Doe Canyon were sampled for produced gas to determine the noble gas and stable isotope signature of the original injected EOR gas and to confirm the source of this naturally-occurring CO 2 . As expected, the natural CO 2 produced from McElmo Dome and Doe Canyon is a mix of mantle and crustal sources. When comparing CO 2 injection and production rates for the CO 2 floods in the North Ward Estes Field, it appears that CO 2 retention in the reservoir decreased over the course of the three injections, retaining 39%, 49% and 61% of the injected CO 2 for the 2008, 2010, and 2013 projects, respectively, characteristic of maturing CO 2 miscible flood projects. Noble gas isotopic composition of the injected and produced gas for the flood projects suggest no active fractionation, while δ 13 C CO 2 values suggest no active CO 2 dissolution into formation water, or mineralization. CO 2 volumes capable of dissolving in residual formation fluids were also estimated along with the potential to store pure-phase supercritical CO 2 . Using a combination of dissolution trapping and residual trapping, both volumes of CO 2 currently retained in the 2008 and 2013 projects could be justified, suggesting no major leakage is occurring. These subsurface reservoirs, jointly considered, have the capacity to store up to 9 years of CO 2 emissions from an average US powerplant.

International Journal of Greenhouse Gas Control↗

USGS2015

U.S. Geological Survey Noble Gas Laboratory’s standard operating procedures for the measurement of dissolved gas in water samples

This report addresses the standard operating procedures used by the U.S. Geological Survey’s Noble Gas Laboratory in Denver, Colorado, U.S.A., for the measurement of dissolved gases (methane, nitrogen, oxygen, and carbon dioxide) and noble gas isotopes (helium-3, helium-4, neon-20, neon-21, neon-22, argon-36, argon-38, argon-40, kryton-84, krypton-86, xenon-103, and xenon-132) dissolved in water. A synopsis of the instrumentation used, procedures followed, calibration practices, standards used, and a quality assurance and quality control program is presented. The report outlines the day-to-day operation of the Residual Gas Analyzer Model 200, Mass Analyzer Products Model 215–50, and ultralow vacuum extraction line along with the sample handling procedures, noble gas extraction and purification, instrument measurement procedures, instrumental data acquisition, and calculations for the conversion of raw data from the mass spectrometer into noble gas concentrations per unit mass of water analyzed. Techniques for the preparation of artificial dissolved gas standards are detailed and coupled to a quality assurance and quality control program to present the accuracy of the procedures used in the laboratory.

Techniques and Methods↗

USGS2015

High influx of carbon in walls of agglutinated foraminifers during the Permian-Triassic transition in global oceans

The Permian – Triassic mass extinction is postulated to be related to the rapid volcanism that produced the Siberian flood basalt (Traps). Unrelated volcanic eruptions producing several episodes of ash falls synchronous with the Siberian Traps are found in South China and Australia. Such regional eruptions could have caused wildfires, burning of coal deposits, and the dispersion of coal fly ash. These eruptions introduced a major influx of carbon into the atmosphere and oceans that can be recognized in the wall structure of foraminiferal tests present in survival populations in the boundary interval strata. Analysis of free specimens of foraminifers recovered from residues of conodont samples taken at a Permian – Triassic boundary section at Lung Cam in northern Vietnam has revealed the presence of a significant amount of elemental carbon , along with oxygen and silica, in their test wall structure, but an absence of calcium carbonate . These foraminifers , identified as Rectocornuspira kalhori , Cornuspira mahajeri , and Earlandia spp. and whose tests previously were considered to be calcareous, are confirmed to be agglutinated , and are now referred to as Ammodiscus kalhori and Hyperammina deformis . Measurement of the 207 Pb/ 204 Pb ratios in pyrite clusters attached to the foraminiferal tests confirmed that these tests inherited the Pb in their outer layer from carbon -contaminated seawater. We conclude that the source of the carbon could have been either global coal fly ash or forest fire-dispersed carbon , or a combination of both, that was dispersed into the Palaeo-Tethys Ocean immediately after the end- Permian extinction event.

Ha Giang Province↗

USGS2015

Magmatic gas emissions at Holocene volcanic features near Mono Lake, California, and their relation to regional magmatism

Silicic lavas have erupted repeatedly in the Mono Basin over the past few thousand years, forming the massive domes and coulees of the Mono Craters chain and the smaller island vents in Mono Lake. We report here on the first systematic study of magmatic CO 2 emissions from these features, conducted during 2007–2010. Most notably, a known locus of weak steam venting on the summit of North Coulee is actually enclosed in a large area (~ 0.25 km 2 ) of diffuse gas discharge that emits 10–14 t/d of CO 2 , mostly at ambient temperature. Subsurface gases sampled here are heavily air-contaminated, but after standard corrections are applied, show average δ 13 C-CO 2 of − 4.72&permil;, 3 He/ 4 He of 5.89R A , and CO 2 / 3 He of 0.77 × 10 10 , very similar to the values in fumarolic gas from Mammoth Mountain and the Long Valley Caldera immediately to the south of the basin. If these values also characterize the magmatic gas source at Mono Lake, where CO 2 is captured by the alkaline lake water, a magmatic CO 2 upflow beneath the lake of ~ 4 t/d can be inferred. Groundwater discharge from the Mono Craters area transports ~ 13 t/d of 14 C-dead CO 2 as free gas and dissolved carbonate species, and adding in this component brings the estimated total magmatic CO 2 output to 29 t/d for the two silicic systems in the Mono Basin. If these emissions reflect intrusion and degassing of underlying basalt with 0.5 wt.% CO 2 , a modest intrusion rate of 0.00075 km 3 /yr is indicated. Much higher intrusion rates are required to account for CO 2 emissions from Mammoth Mountain and the West Moat of the Long Valley Caldera.

California↗

USGS2015

Origins of geothermal gases at Yellowstone

Gas emissions at the Yellowstone Plateau Volcanic Field (YPVF) reflect open-system mixing of gas species originating from diverse rock types, magmas, and crustal fluids, all combined in varying proportions at different thermal areas. Gases are not necessarily in chemical equilibrium with the waters through which they vent, especially in acid sulfate terrain where bubbles stream through stagnant acid water. Gases in adjacent thermal areas often can be differentiated by isotopic and gas ratios, and cannot be tied to one another solely by shallow processes such as boiling-induced fractionation of a parent liquid. Instead, they inherit unique gas ratios (e.g., CH 4 /He) from the dominant rock reservoirs where they originate, some of which underlie the Quaternary volcanic rocks. Steam/gas ratios (essentially H 2 O/CO 2 ) of Yellowstone fumaroles correlate with Ar/He and N 2 /CO 2 , strongly suggesting that H 2 O/CO 2 is controlled by addition of steam boiled from water rich in atmospheric gases. Moreover, H 2 O/CO 2 varies systematically with geographic location, such that boiling is more enhanced in some areas than others. The δ 13 C and 3 He/CO 2 of gases reflect a dominant mantle origin for CO 2 in Yellowstone gas. The mantle signature is most evident at Mud Volcano, which hosts gases with the lowest H 2 O/CO 2 , lowest CH 4 concentrations and highest He isotope ratios (~16Ra), consistent with either a young subsurface intrusion or less input of crustal and meteoric gas than any other location at Yellowstone. Across the YPVF, He isotope ratios ( 3 He/ 4 He) inversely vary with He concentrations, and reflect varied amounts of long- stored, radiogenic He added to the magmatic endmember within the crust. Similarly, addition of CH4 from organic-rich sediments is common in the eastern thermal areas at Yellowstone. Overall, Yellowstone gases reflect addition of deep, high-temperature magmatic gas (CO 2 -rich), lower-temperatures crustal gases ( 4 He- and CH 4 -bearing), and those gases (N 2 , Ne, Ar) added principally through boiling of the meteoric-water-derived geothermal liquid found in the upper few kilometers. We also briefly explore the pathways by which Cl, F, and S, move through the crust.

Montana, Wyoming↗

USGS2014

Quality and age of shallow groundwater in the Bakken Formation production area, Williston Basin, Montana and North Dakota

The quality and age of shallow groundwater in the Bakken Formation production area were characterized using data from 30 randomly distributed domestic wells screened in the upper Fort Union Formation. Comparison of inorganic and organic chemical concentrations to health based drinking-water standards, correlation analysis of concentrations with oil and gas well locations, and isotopic data give no indication that energy-development activities affected groundwater quality. It is important, however, to consider these results in the context of groundwater age. Most samples were recharged before the early 1950s and had 14C ages ranging from 30,000 years. Thus, domestic wells may not be as well suited for detecting contamination associated with recent surface spills as shallower wells screened near the water table. Old groundwater could be contaminated directly by recent subsurface leaks from imperfectly cemented oil and gas wells, but horizontal groundwater velocities calculated from 14C ages imply that the contaminants would still be less than 0.5 km from their source. For the wells sampled in this study, the median distance to the nearest oil and gas well was 4.6 km. Because of the slow velocities, a long-term commitment to groundwater monitoring in the upper Fort Union Formation is needed to assess the effects of energy development on groundwater quality. In conjunction with that effort, monitoring could be done closer to energy-development activities to increase the likelihood of early detection of groundwater contamination if it did occur.

Montana, North Dakota↗

USGS2014

Prodigious degassing of a billion years of accumulated radiogenic helium at Yellowstone

Helium is used as a critical tracer throughout the Earth sciences, where its relatively simple isotopic systematics is used to trace degassing from the mantle, to date groundwater and to time the rise of continents 1 . The hydrothermal system at Yellowstone National Park is famous for its high helium-3/helium-4 isotope ratio, commonly cited as evidence for a deep mantle source for the Yellowstone hotspot 2 . However, much of the helium emitted from this region is actually radiogenic helium-4 produced within the crust by α-decay of uranium and thorium. Here we show, by combining gas emission rates with chemistry and isotopic analyses, that crustal helium-4 emission rates from Yellowstone exceed (by orders of magnitude) any conceivable rate of generation within the crust. It seems that helium has accumulated for (at least) many hundreds of millions of years in Archaean (more than 2.5 billion years old) cratonic rocks beneath Yellowstone, only to be liberated over the past two million years by intense crustal metamorphism induced by the Yellowstone hotspot. Our results demonstrate the extremes in variability of crustal helium efflux on geologic timescales and imply crustal-scale open-system behaviour of helium in tectonically and magmatically active regions.

Wyoming↗

USGS2014

Noble gas geochemistry investigation of high CO2 natural gas at the LaBarge Platform, Wyoming, USA

A regional sampling of gases from thermal springs near the LaBarge Field, Wyoming, USA to determine the extent of the total carbon dioxide system (TCDS) indicates that the system may extend up to 70 km to the northwest of the field. Geochemical evidence from noble gas isotopes, stable element isotopes, and gas composition provide the foundation for these conclusions. Samples from Soda Springs to the west and Grand Teton National Park to the north do not exhibit the potentially diagnostic LaBarge gas chemistry and represent an absolute maximum potential extent of the system. Additional sampling to the south and east as well as in-fill sampling in regions previously sampled are necessary to refine these preliminary TCDS boundaries.

Wyoming↗

USGS2014

Noble gas isotopes in mineral springs within the Cascadia Forearc, Washington and Oregon

This U.S. Geological Survey report presents laboratory analyses along with field notes for a pilot study to document the relative abundance of noble gases in mineral springs within the Cascadia forearc of Washington and Oregon. Estimates of the depth to the underlying Juan de Fuca oceanic plate beneath the sample sites are derived from the McCrory and others (2012) slab model. Some of these springs have been previously sampled for chemical analyses (Mariner and others, 2006), but none currently have publicly available noble gas data. Helium isotope values as well as the noble gas values and ratios presented below will be used to determine the sources and mixing history of these mineral waters.

Oregon;Washington↗

USGS2014

Geochemical investigation of the hydrothermal system on Akutan Island, Alaska, July 2012

We have studied the geochemistry of the hot springs on Akutan Island in detail for the first time since the early 1980s. Springs in four discrete groups (A-D) along Hot Springs Creek showed generally higher temperatures and substantially higher Na, Ca, and Cl concentrations than previously reported, and total hot-spring discharge has also increased markedly. The springs now account for a heat output of ~29 MW, about an order of magnitude more than in 1981. Gas samples from the hot springs and from a fumarolic area on the flank of Akutan Volcano show high 3 He/ 4 He ratios (>6.4 RA) after correction for air contamination and reveal a common magmatic heat source. Hot-spring gases are unusually rich in N 2 , Ar, and CH 4 , suggesting that the water has boiled and lost CO 2 during upflow beneath the flank fumarole field. Gas geothermometry calculations applied to the flank fumarole field implies temperatures of 200–240 °C for the reservoir, and Na-K-Ca geothermometry implies temperatures near 180 °C for the outflow waters that feed the hot springs. The results of our study confirm the existence of a substantial geothermal resource on the island.

Alaska↗

USGS2013

Groundwater ages and mixing in the Piceance Basin natural gas province, Colorado

Reliably identifying the effects of energy development on groundwater quality can be difficult because baseline assessments of water quality completed before the onset of energy development are rare and because interactions between hydrocarbon reservoirs and aquifers can be complex, involving both natural and human processes. Groundwater age and mixing data can strengthen interpretations of monitoring data from those areas by providing better understanding of the groundwater flow systems. Chemical, isotopic, and age tracers were used to characterize groundwater ages and mixing with deeper saline water in three areas of the Piceance Basin natural gas province. The data revealed a complex array of groundwater ages (<10 to >50,000 years) and mixing patterns in the basin that helped explain concentrations and sources of methane in groundwater. Age and mixing data also can strengthen the design of monitoring programs by providing information on time scales at which water quality changes in aquifers might be expected to occur. This information could be used to establish maximum allowable distances of monitoring wells from energy development activity and the appropriate duration of monitoring.

Colorado↗

USGS2013

Evidence for high salinity of Early Cretaceous sea water from the Chesapeake Bay crater

High salinity groundwater more than 1000 metres deep in the Atlantic Coastal Plain of the United States has been documented in several locations1,2, most recently within the 35 million-year-old Chesapeake Bay impact crater3,4,5. Suggestions for the origin of increased salinity in the crater have included evaporite dissolution6, osmosis6, and evaporation from heating7 associated with the bolide impact. Here we present chemical, isotopic and physical evidence that together indicate that groundwater in the Chesapeake crater is remnant Early Cretaceous North Atlantic (ECNA) seawater. We find that the seawater is likely 100-145 million years old and that it has an average salinity of about 70 per mil, which is twice that of modern seawater and consistent with the nearly closed ECNA basin8. Previous evidence for temperature and salinity levels of ancient oceans have been estimated indirectly from geochemical, isotopic and paleontological analyses of solid materials in deep sediment cores. In contrast, our study identifies ancient seawater in situ and provides a direct estimate of its age and salinity. Moreover, we suggest that it is likely that remnants of ECNA seawater persist in deep sediments at many locations along the Atlantic margin.

Maryl;Virginia↗

USGS2013

Tracing groundwater with low-level detections of halogenated VOCs in a fractured carbonate-rock aquifer, Leetown Science Center, West Virginia, USA

Measurements of low-level concentrations of halogenated volatile organic compounds (VOCs) and estimates of groundwater age interpreted from 3 H/ 3 He and SF 6 data have led to an improved understanding of groundwater flow, water sources, and transit times in a karstic, fractured, carbonate-rock aquifer at the Leetown Science Center (LSC), West Virginia. The sum of the concentrations of a set of 16 predominant halogenated VOCs (TDVOC) determined by gas chromatography with electron-capture detector (GC–ECD) exceeded that possible for air–water equilibrium in 34 of the 47 samples (median TDVOC of 24,800 pg kg −1 ), indicating that nearly all the water sampled in the vicinity of the LSC has been affected by addition of halogenated VOCs from non-atmospheric source(s). Leakage from a landfill that was closed and sealed nearly 20 a prior to sampling was recognized and traced to areas east of the LSC using low-level detection of tetrachloroethene (PCE), methyl chloride (MeCl), methyl chloroform (MC), dichlorodifluoromethane (CFC-12), and cis-1,2-dichloroethene (cis-1,2-DCE). Chloroform (CHLF) was the predominant VOC in water from domestic wells surrounding the LSC, and was elevated in groundwater in and near the Fish Health Laboratory at the LSC, where a leak of chlorinated water occurred prior to 2006. The low-level concentrations of halogenated VOCs did not exceed human or aquatic-life health criteria, and were useful in providing an awareness of the intrinsic susceptibility of the fractured karstic groundwater system at the LSC to non-atmospheric anthropogenic inputs. The 3 H/ 3 He groundwater ages of spring discharge from the carbonate rocks showed transient behavior, with ages averaging about 2 a in 2004 following a wet climatic period (2003–2004), and ages in the range of 4–7 a in periods of more average precipitation (2008–2009). The SF 6 and CFC-12 data indicate older water (model ages of 10s of years or more) in the low-permeability shale of the Martinsburg Formation located to the west of the LSC. A two-a record of specific conductance, water temperature, and discharge recorded at 30-min intervals demonstrated an approximately 3-month lag in discharge at Gray Spring. The low groundwater ages of waters from the carbonate rocks support rapid advective transport of contaminants from the LSC vicinity, yet the nearly ubiquitous occurrence of low-level concentrations of halogenated VOCs at the LSC suggests the presence of long-term persistent sources, such as seepage from the closed and sealed landfill, infiltration of VOCs that may persist locally in the epikarst, exchange with low-permeability zones in fractured rock, and upward leakage of older water that may contain elevated concentrations of halogenated VOCs from earlier land use activities.

West Virginia↗

USGS2013

Mass fractionation of noble gases in synthetic methane hydrate: Implications for naturally occurring gas hydrate dissociation

As a consequence of contemporary or longer term (since 15 ka) climate warming, gas hydrates in some settings may presently be dissociating and releasing methane and other gases to the ocean-atmosphere system. A key challenge in assessing the impact of dissociating gas hydrates on global atmospheric methane is the lack of a technique able to distinguish between methane recently released from gas hydrates and methane emitted from leaky thermogenic reservoirs, shallow sediments (some newly thawed), coal beds, and other sources. Carbon and deuterium stable isotopic fractionation during methane formation provides a first-order constraint on the processes (microbial or thermogenic) of methane generation. However, because gas hydrate formation and dissociation do not cause significant isotopic fractionation, a stable isotope-based hydrate-source determination is not possible. Here, we investigate patterns of mass-dependent noble gas fractionation within the gas hydrate lattice to fingerprint methane released from gas hydrates. Starting with synthetic gas hydrate formed under laboratory conditions, we document complex noble gas fractionation patterns in the gases liberated during dissociation and explore the effects of aging and storage (e.g., in liquid nitrogen), as well as sampling and preservation procedures. The laboratory results confirm a unique noble gas fractionation pattern for gas hydrates, one that shows promise in evaluating modern natural gas seeps for a signature associated with gas hydrate dissociation.

Chemical Geology↗

USGS2013

Chemistry and age of groundwater in the Piceance structural basin, Rio Blanco County, Colorado, 2010-12

Fourteen monitoring wells were sampled by the U.S. Geological Survey, in cooperation with the Bureau of Land Management, to better understand the chemistry and age of groundwater in the Piceance structural basin in Rio Blanco County, Colorado, and how they may relate to the development of underlying natural-gas reservoirs. Natural gas extraction in the area has been ongoing since at least the 1950s, and the area contains about 960 producing, shut-in, and abandoned natural-gas wells.

Colorado↗