A crucial component in sustainable freshwater management is the reliable and cost-effective characterization of ground-water aquifers. A technique that allows noninvasive characterization of shallow (<100 m) aquifers is surface nuclear magnetic resonance (surface NMR). The measured parameter longitudinal relaxation time T-1 provides a link to pore-scale properties and can be used to estimate the hydraulic conductivity of the sampled region. The recent development of an optimized acquisition scheme, phase-cycled pseudosaturation recovery (pcPSR), has significantly advanced our ability to acquire surface-NMR T-1 data. Building on these findings, we developed an inversion scheme that can reconstruct the depth-distribution of T-1 from pcPSR data. To stabilize the inversion, we took a staggered approach: We first determined the distribution of water content and effective transverse relaxation time T-2*, and then we resolved the T-1 structure. We tested the capability of the inversion in a synthetic study using models containing an unconfined and confined aquifer under conditions of low and high levels of ambient electromagnetic noise. The results allowed us to optimize the design of pcPSR experiments, finding that acquiring pcPSR data at three interpulse delay times is the best choice when acquiring surface-NMR data in an area with no prior information. We have verified our inversion approach in a field study in Nebraska, USA, where we had access to borehole lithologic information and logging-NMR T-1 measurements. Although the structural details (<1 m) detected in logging NMR were not resolved in surface NMR - highlighting the general resolution limitation of surface NMR - the two methods consistently revealed a zone of elevated T-1 corresponding to a sand and gravel unit, overlying a zone of lower T-1 corresponding to a sand/sandstone unit. Our developed inversion scheme is an important step toward the reliable interpretation of surface-NMR T-1 data for aquifer characterization.
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Kings Coll London, Div Imaging Sci & Biomed Engn, London, England
Beth Israel Deaconess Med Ctr, Dept Med, Boston, MA 02215 USA
Harvard Med Sch, Boston, MA 02115 USAKings Coll London, Div Imaging Sci & Biomed Engn, London, England
Nezafat, Maryam
Ramos, Isabel T.
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Kings Coll London, Div Imaging Sci & Biomed Engn, London, EnglandKings Coll London, Div Imaging Sci & Biomed Engn, London, England
Ramos, Isabel T.
Henningsson, Markus
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Kings Coll London, Div Imaging Sci & Biomed Engn, London, EnglandKings Coll London, Div Imaging Sci & Biomed Engn, London, England
Henningsson, Markus
Pratti, Andrea
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Kings Coll London, Div Imaging Sci & Biomed Engn, London, EnglandKings Coll London, Div Imaging Sci & Biomed Engn, London, England
Pratti, Andrea
Basha, Tamer
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Cairo Univ, Biomed Engn Dept, Giza, EgyptKings Coll London, Div Imaging Sci & Biomed Engn, London, England
Basha, Tamer
Botnar, Rene M.
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Kings Coll London, Div Imaging Sci & Biomed Engn, London, England
Pontificia Univ Catolica Chile, Escuela Ingn, Santiago, ChileKings Coll London, Div Imaging Sci & Biomed Engn, London, England