Hillegonds Darren

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Hillegonds
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Darren
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  • Article
    Basin architecture controls on the chemical evolution and 4He distribution of groundwater in the Paradox Basin
    (Elsevier, 2022-05-11) Tyne, Rebecca L. ; Barry, Peter H. ; Cheng, Anran ; Hillegonds, Darren ; Kim, Ji-Hyun ; McIntosh, Jennifer C. ; Ballentine, Christopher J.
    Fluids such as 4He, H2, CO2 and hydrocarbons accumulate within Earth's crust. Crustal reservoirs also have potential to store anthropogenic waste (e.g., CO2, spent nuclear fuel). Understanding fluid migration and how this is impacted by basin stratigraphy and evolution is key to exploiting fluid accumulations and identifying viable storage sites. Noble gases are powerful tracers of fluid migration and chemical evolution, as they are inert and only fractionate by physical processes. The distribution of 4He, in particular, is an important tool for understanding diffusion within basins and for groundwater dating. Here, we report noble gas isotope and abundance data from 36 wells across the Paradox Basin, Colorado Plateau, USA, which has abundant hydrocarbon, 4He and CO2 accumulations. Both groundwater and hydrocarbon samples were collected from 7 stratigraphic units, including within, above and below the Paradox Formation (P.Fm) evaporites. Air-corrected helium isotope ratios (0.0046 - 0.127 RA) are consistent with radiogenic overprinting of predominantly groundwater-derived noble gases. The highest radiogenic noble gas concentrations are found in formations below the P.Fm. Atmosphere-derived noble gas signatures are consistent with meteoric recharge and multi-phase interactions both above and below the P.Fm, with greater groundwater-gas interactions in the shallower formations. Vertical diffusion models, used to reconstruct observed groundwater helium concentrations, show the P.Fm evaporite layer to be effectively impermeable to helium diffusion and a regional barrier for mobile elements but, similar to other basins, a basement 4He flux is required to accumulate the 4He concentrations observed beneath the P.Fm. The verification that evaporites are regionally impermeable to diffusion, of even the most diffusive elements, is important for sub-salt helium and hydrogen exploration and storage, and a critical parameter in determining 4He-derived mean groundwater ages. This is critical to understanding the role of basin stratigraphy and deformation on fluid flow and gas accumulation.
  • Article
    Rapid microbial methanogenesis during CO2 storage in hydrocarbon reservoirs
    (Nature Research, 2021-12-22) Tyne, Rebecca L. ; Barry, Peter H. ; Lawson, Michael ; Byrne, David J. ; Warr, Oliver ; Xie, Hao ; Hillegonds, Darren ; Formolo, Michael ; Summers, Zara M. ; Skinner, Brandon ; Eiler, John M. ; Ballentine, Christopher J.
    Carbon capture and storage (CCS) is a key technology to mitigate the environmental impact of carbon dioxide (CO2) emissions. An understanding of the potential trapping and storage mechanisms is required to provide confidence in safe and secure CO2 geological sequestration1,2. Depleted hydrocarbon reservoirs have substantial CO2 storage potential1,3, and numerous hydrocarbon reservoirs have undergone CO2 injection as a means of enhanced oil recovery (CO2-EOR), providing an opportunity to evaluate the (bio)geochemical behaviour of injected carbon. Here we present noble gas, stable isotope, clumped isotope and gene-sequencing analyses from a CO2-EOR project in the Olla Field (Louisiana, USA). We show that microbial methanogenesis converted as much as 13–19% of the injected CO2 to methane (CH4) and up to an additional 74% of CO2 was dissolved in the groundwater. We calculate an in situ microbial methanogenesis rate from within a natural system of 73–109 millimoles of CH4 per cubic metre (standard temperature and pressure) per year for the Olla Field. Similar geochemical trends in both injected and natural CO2 fields suggest that microbial methanogenesis may be an important subsurface sink of CO2 globally. For CO2 sequestration sites within the environmental window for microbial methanogenesis, conversion to CH4 should be considered in site selection.
  • Article
    A novel method for the extraction, purification, and characterization of noble gases in produced fluids
    (Wiley, 2019-10-14) Tyne, Rebecca L. ; Barry, Peter H. ; Hillegonds, Darren ; Hunt, Andrew G. ; Kulongoski, Justin T. ; Stephens, Michael J. ; Byrne, David J. ; Ballentine, Christopher J.
    Hydrocarbon systems with declining or viscous oil production are often stimulated using enhanced oil recovery (EOR) techniques, such as the injection of water, steam, and CO2, in order to increase oil and gas production. As EOR and other methods of enhancing production such as hydraulic fracturing have become more prevalent, environmental concerns about the impact of both new and historical hydrocarbon production on overlying shallow aquifers have increased. Noble gas isotopes are powerful tracers of subsurface fluid provenance and can be used to understand the impact of EOR on hydrocarbon systems and potentially overlying aquifers. In oil systems, produced fluids can consist of a mixture of oil, water and gas. Noble gases are typically measured in the gas phase; however, it is not always possible to collect gases and therefore produced fluids (which are water, oil, and gas mixtures) must be analyzed. We outline a new technique to separate and analyze noble gases in multiphase hydrocarbon‐associated fluid samples. An offline double capillary method has been developed to quantitatively isolate noble gases into a transfer vessel, while effectively removing all water, oil, and less volatile hydrocarbons. The gases are then cleaned and analyzed using standard techniques. Air‐saturated water reference materials (n = 24) were analyzed and results show a method reproducibility of 2.9% for 4He, 3.8% for 20Ne, 4.5% for 36Ar, 5 .3% for 84Kr, and 5.7% for 132Xe. This new technique was used to measure the noble gas isotopic compositions in six produced fluid samples from the Fruitvale Oil Field, Bakersfield, California.
  • Article
    Gas emissions and subsurface architecture of fault‐controlled geothermal systems: a case study of the North Abaya Geothermal Area
    (American Geophysical Union, 2023-03-30) Hutchison, William ; Ogilvie, Euan R. D. ; Birhane, Yafet G. ; Barry, Peter H. ; Fischer, Tobias P. ; Ballentine, Chris J. ; Hillegonds, Darren J. ; Biggs, Juliet ; Albino, Fabien ; Cervantes, Chelsea ; Guðbrandsson, Snorri
    East Africa hosts significant reserves of untapped geothermal energy. Exploration has focused on geologically young (<1 Ma) silicic calderas, yet there are many sites of geothermal potential where there is no clear link to an active volcano. The origin and architecture of these systems are poorly understood. Here, we combine remote sensing and field observations to investigate a fault‐controlled geothermal play located north of Lake Abaya in the Main Ethiopian Rift. Soil gas CO2 and temperature surveys were used to examine permeable pathways and showed elevated values along a ∼110 m high fault, which marks the western edge of the Abaya graben. Ground temperatures are particularly elevated where multiple intersecting faults form a wedged horst structure. This illustrates that both deep penetrating graben bounding faults and near‐surface fault intersections control the ascent of hydrothermal fluids and gases. Total CO2 emissions along the graben fault are ∼300 t d−1; a value comparable to the total CO2 emission from silicic caldera volcanoes. Fumarole gases show δ13C of −6.4‰ to −3.8‰ and air‐corrected 3He/4He values of 3.84–4.11 RA, indicating a magmatic source originating from an admixture of upper mantle and crustal helium. Although our model of the North Abaya geothermal system requires a deep intrusive heat source, we find no ground deformation evidence for volcanic unrest or recent volcanism along the graben fault. This represents a key advantage over the active silicic calderas that typically host these resources and suggests that fault‐controlled geothermal systems offer viable prospects for geothermal exploration.
  • Article
    Investigating the effect of enhanced oil recovery on the noble gas signature of casing gases and produced waters from selected California oil fields
    (Elsevier, 2021-09-25) Tyne, Rebecca L. ; Barry, Peter H. ; Karolytė, Rūta ; Byrne, David J. ; Kulongoski, Justin T. ; Hillegonds, Darren ; Ballentine, Christopher J.
    In regions where water resources are scarce and in high demand, it is important to safeguard against contamination of groundwater aquifers by oil-field fluids (water, gas, oil). In this context, the geochemical characterisation of these fluids is critical so that anthropogenic contaminants can be readily identified. The first step is characterising pre-development geochemical fluid signatures (i.e., those unmodified by hydrocarbon resource development) and understanding how these signatures may have been perturbed by resource production, particularly in the context of enhanced oil recovery (EOR) techniques. Here, we present noble gas isotope data in fluids produced from oil wells in several water-stressed regions in California, USA, where EOR is prevalent. In oil-field systems, only casing gases are typically collected and measured for their noble gas compositions, even when oil and/or water phases are present, due to the relative ease of gas analyses. However, this approach relies on a number of assumptions (e.g., equilibrium between phases, water-to-oil ratio (WOR) and gas-to-oil ratio (GOR) in order to reconstruct the multiphase subsurface compositions. Here, we adopt a novel, more rigorous approach, and measure noble gases in both casing gas and produced fluid (oil-water-gas mixtures) samples from the Lost Hills, Fruitvale, North and South Belridge (San Joaquin Basin, SJB) and Orcutt (Santa Maria Basin) Oil Fields. Using this method, we are able to fully characterise the distribution of noble gases within a multiphase hydrocarbon system. We find that measured concentrations in the casing gases agree with those in the gas phase in the produced fluids and thus the two sample types can be used essentially interchangeably. EOR signatures can readily be identified by their distinct air-derived noble gas elemental ratios (e.g., 20Ne/36Ar), which are elevated compared to pre-development oil-field fluids, and conspicuously trend towards air values with respect to elemental ratios and overall concentrations. We reconstruct reservoir 20Ne/36Ar values using both casing gas and produced fluids and show that noble gas ratios in the reservoir are strongly correlated (r2 = 0.88–0.98) to the amount of water injected within ~500 m of a well. We suggest that the 20Ne/36Ar increase resulting from injection is sensitive to the volume of fluid interacting with the injectate, the effective water-to-oil ratio, and the composition of the injectate. Defining both the pre-development and injection-modified hydrocarbon reservoir compositions are crucial for distinguishing the sources of hydrocarbons observed in proximal groundwaters, and for quantifying the transport mechanisms controlling this occurrence.