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Geology topics

Brian W. Stewart

Publications and source records attributed to Brian W. Stewart.

3 recordsLinked to original sources

Unified 200 kyr paleohydrologic history of the Southern Great Basin: Death Valley, Searles Valley, Owens Valley and the Devils Hole cave

We present a hydroclimate synthesis of the southern Great Basin over the last two glacial-interglacial cycles focused on paleolakes in Death Valley (core DV93-1), Searles Valley (core SLAPP-SRLS17), Owens Valley (core OL92), and the Devils Hole cave. There is close agreement between the occurrence of lakes in Death Valley and the height of the water table in the Devils Hole (50 km east of Death Valley) during the last 200 kyr. Death Valley and Devils Hole have adjacent, partly overlapping, drainage areas and most likely did over the last 200 kyr. When the water table in the Devils Hole was above the threshold level of ∼5 m higher than the modern, permanent lakes existed in Death Valley. At water table elevations less than 5 m above the modern, ephemeral lakes, saline pans, and mudflats occurred in Death Valley. The close temporal agreement between inferred paleoenvironments from the sediments in the Death Valley core and the paleowater table elevation in Devils Hole suggests a common forcing and provides insight into climate variability in the southwestern United States over the last 200 kyr. Owens Valley and Searles Valley, which derived inflow waters from the Sierra Nevada via the Owens River, contain paleohydrologic records which match those from Death Valley and the Devils Hole in terms of timing and direction of water availability over the last 200 kyr, indicating a similar paleohydrologic history for the entire southern Great Basin region. Near the end of Marine Oxygen Isotope Stage 6 (MIS 6), 140 ka - 130 ka, Lake Manly in Death Valley became shallow and hypersaline, and ultimately dried up at 127.1 ka ±4.3 ka. The transition from glacial to interglacial vegetation, which involved the loss of Juniperus pollen and an increase in Quercus (oak) pollen, occurred in Death Valley core DV93-1 at 131.3 ka ±4.0 ka. Following the glacial to interglacial pollen shift, a large alkaline lake formed in Death Valley. Similar conditions (freshwater, high productivity, and a mixed, deeply oxygenated water column indicated by biomarkers) existed in Searles Lake between 135.3 +2.7 / -2.9 ka and 130.1 +2.7 / -2.6 ka, also following the juniper-oak pollen transition. Sr isotopes in calcite and sulfate minerals (gypsum, glauberite, thenardite), and the rare occurrence of the sodium carbonate mineral northupite with a low 87 Sr/ 86 Sr ratio in core DV93-1, together with organic geochemical proxies from Searles core SLAPP-SRLS17, all suggest that at this time, late MIS 6 Lake Manly in Death Valley received alkaline water via spillover from Searles Valley into Death Valley through Panamint Valley. The hydrologic connection between Searles Valley, Panamint Valley, and Death Valley at Termination II (130 ka) is documented here for this system of pluvial lakes for the first time. The Devils Hole water table decreased to +6.5 m at 140.8 ka ±3.2 ka, rose briefly to +8 m at 137.6 ka ±0.5 ka, and then dropped 8 m by 120.36 ka ±0.45 ka, when it reached an elevation similar to the modern. The pluvial lakes in Death Valley and Searles Valley may have coincided with the rise of the Devils Hole water table at ∼137.6 ka ±0.5 ka years ago, although the age models for core DV93-1 and core SLAPP-SLRS17 during the end of MIS 6 carry large uncertainties.

Quaternary Science Reviews

Utica/Point Pleasant brine isotopic compositions (δ7Li, δ11B, δ138Ba) elucidate mechanisms of lithium enrichment in the Appalachian Basin

Global Li production will require a ~500 % increase to meet 2050 projected energy storage demands. One potential source is oil and gas wastewater (i.e., produced water or brine), which naturally has high total dissolved solids (TDS) concentrations, that can also be enriched in Li (>100 mg/L). Understanding the sources and mechanisms responsible for high naturally-occurring Li concentrations can aid in efficient targeting of these brines. The isotopic composition (δ 7 Li, δ 11 B, δ 138 Ba) of produced water and core samples from the Utica Shale and Point Pleasant Formation (UPP) in the Appalachian Basin, USA indicates that depth-dependent thermal maturity and water-rock interaction, including diagenetic clay mineral transformations, likely control Li concentrations. A survey of Li content in produced waters throughout the USA indicates that Appalachian Basin brines from the Marcellus Shale to the UPP have the potential for economic resource recovery.

Maryland, Ohio, Pennsylvania, West Virginia

Factors controlling Li concentration and isotopic composition in formation waters and host rocks of Marcellus Shale, Appalachian Basin

In this study, water and whole rock samples from hydraulically fractured wells in the Marcellus Shale (Middle Devonian), and water from conventional wells producing from Upper Devonian sandstones were analyzed for lithium concentrations and isotope ratios (&delta; 7 Li). The distribution of lithium concentrations in different mineral groups was determined using sequential extraction. Structurally bound Li, predominantly in clays, accounted for 75-91 wt. % of total Li, whereas exchangeable sites and carbonate cement contain negligible Li (< 3%). Up to 20% of the Li is present in the oxidizable fraction (organic matter and sulfides). The &delta; 7 Li values for whole rock shale in Greene Co., Pennsylvania, and Tioga Co., New York, ranged from -2.3 to + 4.3&permil;, similar to values reported for other shales in the literature. The &delta; 7 Li values in shale rocks with stratigraphic depth record progressive weathering of the source region; the most weathered and clay-rich strata with isotopically light Li are found closest to the top of the stratigraphic section. Diagenetic illite-smectite transition could also have partially affected the bulk Li content and isotope ratios of the Marcellus Shale. In Greene Co., southwest Pennsylvania, the Upper Devonian sandstone formation waters have &delta; 7 Li values of + 14.6 &plusmn; 1.2 (2SD, n = 25), and are distinct from Marcellus Shale formation waters which have &delta; 7 Li of + 10.0 &plusmn; 0.8 (2SD, n = 12). These two formation waters also maintain distinctive 87 Sr/ 86 Sr ratios suggesting hydrologic separation between these units. Applying temperature-dependent illitilization model to Marcellus Shale, we found that Li concentration in clay minerals increased with Li concentration in pore fluid during diagenetic illite-smectite transition. Samples from north central PA show a much smaller range in both &delta; 7 Li and 87 Sr/ 86 Sr than in southwest Pennsylvania. Spatial variations in Li and &delta; 7 Li values show that Marcellus formation waters are not homogeneous across the Appalachian Basin. Marcellus formation waters in the northeastern Pennsylvania portion of the basin show a much smaller range in both &delta; 7 Li and 87 Sr/ 86 Sr, suggesting long term, cross-formational fluid migration in this region. Assessing the impact of potential mixing of fresh water with deep formation water requires establishment of a geochemical and isotopic baseline in the shallow, fresh water aquifers, and site specific characterization of formation water, followed by long-term monitoring, particularly in regions of future shale gas development.

New York, Pennsylvania