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Robert J. Bodnar

Robert J. Bodnar

· University Distinguished Professor and C.C. Garvin Professor of GeochemistryVerified

Virginia Tech · Geosciences

Active 1978–2026

h-index69
Citations20.9k
Papers50458 last 5y
Funding$2.2M
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About

Robert J. Bodnar is a University Distinguished Professor and the C. C. Garvin Professor of Geochemistry at Virginia Tech in the Department of Geosciences. He holds a Ph.D. in Geochemistry and Mineralogy from Penn State University, obtained in 1985, and has a background in geology and chemistry from the University of Arizona and the University of Pittsburgh. His research focuses on fluid inclusion studies, experimental geochemistry, and mineralogy, contributing significantly to understanding hydrothermal fluid characteristics, fluid inclusion techniques, and water-rock interactions. Bodnar has authored numerous publications in these fields and has been recognized with various honors and awards for his contributions to geosciences.

Research topics

  • Geochemistry
  • Geology
  • Chemistry
  • Mineralogy
  • Petrology
  • Seismology
  • Paleontology
  • Astrobiology
  • Oceanography
  • Physics
  • Geotechnical engineering
  • Soil science
  • Earth science

Selected publications

  • Rainwater accumulation model related to tectono-stratigraphic assessment for bradyseism at Campi Flegrei, Italy

    Geoscience Frontiers · 2026-01-18

    article
  • Synthetic fluid inclusions: A novel technique for experimental water-rock studies

    2026-02-20 · 1 citations

    article1st authorCorresponding

    Synthetic fluid inclusions have been used to determine volumetric and phase equilibrium properties of fluids over a wide range of pressure-temperature-composition conditions. The technique is particularly useful in the study of immiscible fluid systems and for systems which become saturated in one or more solid or fluid phases during cooling and decompression from experimental to ambient conditions. When used in conjunction with conventional experimental techniques, synthetic fluid inclusions permit determination and quantification of physical properties of fluid systems over the complete range of PTX conditions of interest to geochemists studying crustal geochemical processes.

  • Leveraging Fine-Tuned Large Language Models (LLM) and Retrieval-Augmented Generation (RAG) for Modeling Complex Geological Fluid Systems (Geofluids) at Crustal and Mantle Conditions

    2025-01-01

    article1st authorCorresponding
  • FLUID PULSES DURING SUBDUCTION AND THEIR IMPACTS ON FLUID COMPOSITION, ROCK VOLUME, AND METASOMATISM

    Abstracts with programs - Geological Society of America · 2025-01-01

    articleSenior author
  • Meeting Future U.S. Mineral Resource Needs: The Role of the U.S. Geological Survey Mineral Resources Program

    Abstracts with programs - Geological Society of America · 2025-01-01

    article
  • New insights into the evolution of boron isotope composition of seawater from evaporites

    2025-01-01

    article
  • Review: The hydrogeology of critical mineral resources relevant to the energy transition

    Hydrogeology Journal · 2025-05-31 · 3 citations

    articleOpen access

    Abstract Attaining the goals of the international treaty on climate change (the Paris Agreement) will greatly increase the demand for the critical minerals required to implement clean-energy technologies. This poses both challenges and opportunities to the hydrogeologic community from several perspectives. Here, important insights that the hydrogeological sciences have to offer for mineral exploration, mineral production, and addressing environmental issues related to mining and mine decommissioning are summarized. This study focuses on copper, cobalt, lithium, and rare earths to represent the broad spectrum of critical minerals and illustrate their relevance by referring to projected demands and production rates. The current understanding of the hydrogeologic processes that form major deposits of these minerals are then summarized. Ore is defined as the naturally occurring material from which minerals of economic value can be extracted, where most ore deposits are the products of complex hydrogeologic couplings between fluid flow, heat transport, solute transport, chemical reactions, and mechanical deformation. Exploration models for the discovery of deeper, hidden deposits are potentially informed by hydrogeologic theory and hydrogeochemical processes. Hydrogeologic understanding and methods are also essential to production and recovery. Longstanding challenges are mine dewatering and (conversely) mine water supply, as well as mineral-extraction practices such as spoil heap leaching and in situ mining. New challenges arise from element extraction from subsurface brines. Finally, the quantity of water use and potential environmental impacts of mining on water quality are at the core of ‘social license’: the approval and acceptance of society to mining activities.

  • The role of magma differentiation in optimizing the fluid-assisted extraction of copper to generate large porphyry-type deposits

    Science Advances · 2025-06-25 · 17 citations

    articleOpen access

    Porphyry copper deposits (PCDs) are the main source of copper globally, with the metals transported in and deposited from aqueous magmatic fluids. Processes that define the volume of magma and concentration of copper in the magma required to form PCDs, however, are not well understood. Here, we present the results of quantitative modeling of the behavior of Cu and Cl during magma evolution in the upper crust. We show that fractional crystallization is the most important process promoting efficient Cu extraction, and that high concentrations of Cu in the ore-forming hydrothermal fluids can be reached with moderate Cl concentrations. Unusually high concentrations of Cl and Cu in the magma and large magma volumes are not required. Arc magmas of modest volume (<10 3 km 3 ) and modest initial Cu and Cl concentrations can generate large PCDs, if a sufficient mass of magmatic fluid is exsolved at an advanced stage of crystallization.

  • Magma sources, crustal storage depths, and degassing of alkalic, CO2-rich magmas at Nyiragongo and Nyamulagira Volcanoes, Democratic Republic of the Congo

    Earth and Planetary Science Letters · 2025-06-05 · 2 citations

    articleOpen accessSenior author

    • Melt inclusions contain up to 1.3 wt% CO₂, and primary melts are estimated to have contained 4.4–6.0 wt% CO₂. • Primitive melts crystallized over a range of depths, with maximum values of 10–18 km, whereas more evolved melts crystallized at depths <5 km. • Sources of alkalic magmas are lithospheric mantle metasomes containing amphibole, clinopyroxene, phlogopite, and carbonate. • Degassing models predict CO₂-rich gas compositions that match surficial plume measurements from summit lava lakes. Nyiragongo and Nyamulagira are two of the most active volcanoes in the East African Rift System, producing some of the highest fluxes of volcanic CO₂ and SO₂ on Earth, yet pre-eruptive volatile constraints at these volcanoes remain sparse. Here, we report the geochemistry of melt inclusions (MI) from Mg-rich tephra erupted from flank cones of Nyamulagira and Nyiragongo. In our sample suite, CO₂ concentrations in bubble-corrected melt inclusions reach ∼1.3 and 0.9 wt% for Nyiragongo and Nyamulagira, respectively. Water concentrations are 0.8–1.6 wt% for primitive compositions and 0.2–0.4 wt% for more evolved compositions. Sulfur concentrations reach up to 3100 ppm at Nyiragongo and 2500 ppm at Nyamulagira. Major element ‘fingerprinting’ of MI shows that some tephra samples have MI with both Nyamulagira and Nyiragongo-type compositions, requiring mixing of olivine originally crystallized from multiple distinct magma types. Volatile solubility modeling yields a wide range of crystallization depths for more primitive magmas, with maximum values of ∼10–18 km, compared to <5 km for more evolved magmas erupted at the Nyamulagira summit. Estimated CO₂ concentrations for primary melts based on final equilibration with a lherzolite residue at mantle depths are 6.0 ± 2.5 wt% for Nyiragongo and 4.4 ± 2.5 wt% for Nyamulagira. Major element and volatile data are consistent with magma generation in metasomatized lithospheric mantle domains (metasomes) of amphibole+clinopyroxene+lesser phlogopite, with high initial CO₂ sourced from carbonate phase(s). Degassing models of CO₂, H₂O, and S show that gas compositions at the two volcanoes can be explained by evolved magmas feeding summit lava lakes by a process of conduit convection and degassing.

  • Insights into magma storage depths and eruption controls at Kīlauea Volcano during explosive and effusive periods based on melt and fluid inclusions

    2024-01-01

    articleOpen access

Recent grants

Frequent coauthors

  • Matthew Steele‐MacInnis

    University of Alberta

    37 shared
  • M. E. Zolensky

    33 shared
  • Mantu K. Hudait

    Virginia Tech

    28 shared
  • H. Y. McSween

    University of Tennessee at Knoxville

    25 shared
  • J. Donald Rimstidt

    Virginia Tech

    24 shared
  • L. A. Taylor

    22 shared
  • Hector Lamadrid

    University of Oklahoma

    22 shared
  • Benedetto De Vivo

    Nanjing University

    21 shared

Labs

  • Department of Geosciences, Virginia TechPI

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