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Adolph, G., Römer, T., & Külls, C. Deriving complex groundwater age structure by combining age dating and analytic element modelling. In G-DAT 2008-Leipzig (12).
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Külls, C., Haering, M., Leistert, H., & Oster, H. Hydrological, physical and chemical constraints for groundwater age dating with CFC and SF6. In G-DAT 2008-Leipzig (29).
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Strandmann, P. A. E. P. von, Reynolds, B. C., Porcelli, D., James, R. H., Calsteren, P. van, Baskaran, M., et al. (2006). Assessing continental weathering rates and actinide transport in the Great Artesian Basin. Geochimica et Cosmochimica Acta, 70(18, Supplement), 497.
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Bonnetti, C., Zhou, L., Riegler, T., Brugger, J., & Fairclough, M. (2020). Large S isotope and trace element fractionations in pyrite of uranium roll front systems result from internally-driven biogeochemical cycle. Geochimica et Cosmochimica Acta, 282, 113–132.
Abstract: Complex pyrite textures associated with large changes in isotopic and trace element compositions are routinely assumed to be indicative of multi-faceted processes involving multiple fluid and sulfur sources. We propose that the features of ore-stage pyrite from roll front deposits across the world, revealed in exquisite detail via high-resolution trace element mapping by LA-ICP-MS, reflect the dynamic internal evolution of the biogeochemical processes responsible for sulfate reduction, rather than externally driven changes in fluid or sulfur sources through time. Upon percolation of oxidizing fluids into the reduced host-sandstones, roll front systems become self-organized, with a systematic reset of their activity cycle after each translation stage of the redox interface down dip of the aquifer. Dominantly reducing conditions at the redox interface favor the formation of biogenic framboidal pyrite (δ34S from −30.5 to −12.5‰) by bacterial sulfate reduction and the genesis of the U mineralization. As the oxidation front advances, oxidation of reduced sulfur minerals induces an increased supply of sulfate and metals in solution to the bacterial sulfate reduction zone that has similarly advanced down the flow gradient. Hence, this stage is marked by increased rates of the bacterial sulfate reduction associated with the crystallization of variably As-Co-Ni-Mo-enriched concentric pyrite (up to 10,000′s of ppm total trace contents) with moderately negative δ34S values (from −13.7 to −7.5‰). A final stage of pyrite cement with low trace element contents and heavier δ34S signature (from −6.9 to +18.8‰) marks the end of the roll front activity cycle and the transition from an open to a predominantly closed system behavior (negligible advection of fresh sulfate). Blocky pyrite cement is formed using the remaining sulfate, which now becomes quickly heavy according to a Rayleigh isotope fractionation process. This ends the cycle by depleting the nutrient supplies for the sulfate-reducing bacteria and cementing pore spaces within the host sandstone, effectively restricting fluid infiltration. This internally-driven roll front activity cycle results in systematic, large S isotope and trace element fractionation. Ultimately, the long-time evolution of the basin and fluid sources control the metal endowment and evolution of the system; these events, however, are unlikely to be preserved by the roll front, as a direct result of its hydrodynamic nature.
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Ingham, E. S., Cook, N. J., Cliff, J., Ciobanu, C. L., & Huddleston, A. (2014). A combined chemical, isotopic and microstructural study of pyrite from roll-front uranium deposits, Lake Eyre Basin, South Australia. Geochimica et Cosmochimica Acta, 125, 440–465.
Abstract: The common sulfide mineral pyrite is abundant throughout sedimentary uranium systems at Pepegoona, Pepegoona West and Pannikan, Lake Eyre Basin, South Australia. Combined chemical, isotopic and microstructural analysis of pyrite indicates variation in fluid composition, sulfur source and precipitation conditions during a protracted mineralization event. The results show the significant role played by pyrite as a metal scavenger and monitor of fluid changes in low-temperature hydrothermal systems. In-situ micrometer-scale sulfur isotope analyses of pyrite demonstrated broad-scale isotopic heterogeneity (δ34S=−43.9 to +32.4‰VCDT), indicative of complex, multi-faceted pyrite evolution, and sulfur derived from more than a single source. Preserved textures support this assertion and indicate a genetic model involving more than one phase of pyrite formation. Authigenic pyrite underwent prolonged evolution and recrystallization, evidenced by a genetic relationship between archetypal framboidal aggregates and pyrite euhedra. Secondary hydrothermal pyrite commonly displays hyper-enrichment of several trace elements (Mn, Co, Ni, As, Se, Mo, Sb, W and Tl) in ore-bearing horizons. Hydrothermal fluids of magmatic and meteoric origins supplied metals to the system but the geochemical signature of pyrite suggests a dominantly granitic source and also the influence of mafic rock types. Irregular variation in δ34S, coupled with oscillatory trace element zonation in secondary pyrite, is interpreted in terms of continuous variations in fluid composition and cycles of diagenetic recrystallization. A late-stage oxidizing fluid may have mobilized selenium from pre-existing pyrite. Subsequent restoration of reduced conditions within the aquifer caused ongoing pyrite re-crystallization and precipitation of selenium as native selenium. These results provide the first qualitative constraints on the formation mechanisms of the uranium deposits at Beverley North. Insights into depositional conditions and sources of both sulfide and uranium mineralization and an improved understanding of pyrite geochemistry can also underpin an effective vector for uranium exploration at Beverley North and other sedimentary systems of the Lake Eyre Basin, as well as in comparable geological environments elsewhere.
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Lightfoot, D. R. (1996). Moroccan khettara: Traditional irrigation and progressive desiccation. Geoforum, 27(2), 261–273.
Abstract: A 300 km network of khettara (qanat) subsurface irrigation channels was excavated in the Tafilalt basin beginning in the late 14th century. More than 75 of these chains provided perennial water following the breakup of the ancient city of Sijilmassa. Khettara continued to function for much of the northern oasis until the early 1970s, when new technologies and government policies forced changes. Data on origins, maintenance, and current use were collected from archival sources, aerial photographs, Landsat imagery, and from interviews. Insufficient water resources and unsustainable practices have dramatically lowered the water table, drying up khettara. This has resulted in a loss of local control over water resources, abandonment of a sustainable irrigation system, and progressive desiccation.
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Khaneiki, M. L., Al-Ghafri, A. S., Klöve, B., & Haghighi, A. T. (2022). Sustainability and virtual water: The lessons of history. Geography and Sustainability, 3(4), 358–365.
Abstract: This article aims to show that virtual water has historically been an adaptation strategy that enabled some arid regions to develop a prosperous economy without putting pressure on their scarce water resources. Virtual water is referred to as the total amount of water that is consumed to produce goods and services. As an example, in arid central Iran, the deficiency in agricultural revenues was offset by more investment in local industries that enjoyed a perennial capacity to employ more workers. The revenues of local industries weaned the population from irrigated agriculture, since most of their raw materials and also food stuff were imported from other regions, bringing a remarkable amount of virtual water. This virtual water not only sustained the region’s inhabitants, but also set the stage for a powerful polity in the face of a rapid population growth between the 13th and 15th centuries AD. The resultant surplus products entailed a vast and safe network of roads, provided by both entrepreneurs and government. Therefore, it became possible to import more feedstock such as cocoons from water-abundant regions and then export silk textiles with considerable value-added. This article concludes that a similar model of virtual water can remedy the ongoing water crisis in central Iran, where groundwater reserves are overexploited, and many rural and urban centers are teetering on the edge of socio-ecological collapse. History holds an urgent lesson on sustainability for our today’s policy that stubbornly peruses agriculture and other high-water-demand sectors in an arid region whose development has always been dependent on virtual water.
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Adolph, G., KÜlls, C., & Willscheid, A. (2007). Determination and validation of age structures as an improved measure of hydrological dynamics. In Geophysical Research Abstracts (Vol. 9).
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Lawrinenko, M., Kurwadkar, S., & Wilkin, R. T. (2023). Long-term performance evaluation of zero-valent iron amended permeable reactive barriers for groundwater remediation – A mechanistic approach. Geoscience Frontiers, 14(2), 101494.
Abstract: Permeable reactive barriers (PRBs) are used for groundwater remediation at contaminated sites worldwide. This technology has been efficient at appropriate sites for treating organic and inorganic contaminants using zero-valent iron (ZVI) as a reductant and as a reactive material. Continued development of the technology over the years suggests that a robust understanding of PRB performance and the mechanisms involved is still lacking. Conflicting information in the scientific literature downplays the critical role of ZVI corrosion in the remediation of various organic and inorganic pollutants. Additionally, there is a lack of information on how different mechanisms act in tandem to affect ZVI-groundwater systems through time. In this review paper, we describe the underlying mechanisms of PRB performance and remove isolated misconceptions. We discuss the primary mechanisms of ZVI transformation and aging in PRBs and the role of iron corrosion products. We review numerous sites to reinforce our understanding of the interactions between groundwater contaminants and ZVI and the authigenic minerals that form within PRBs. Our findings show that ZVI corrosion products and mineral precipitates play critical roles in the long-term performance of PRBs by influencing the reactivity of ZVI. Pore occlusion by mineral precipitates occurs at the influent side of PRBs and is enhanced by dissolved oxygen and groundwater rich in dissolved solids and high alkalinity, which negatively impacts hydraulic conductivity, allowing contaminants to potentially bypass the treatment zone. Further development of site characterization tools and models is needed to support effective PRB designs for groundwater remediation.
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Döll, P., Krol, M., Fuhr, D., Gaiser, T., Herfort, J., Höynck, S., et al. (2003). Integrated scenarios of regional development in Ceará and Piauí. In Global Change and Regional Impacts (pp. 19–41). Springer, Berlin, Heidelberg.
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