Recovery of Injected Freshwater from a Brackish Aquifer with a Multiwell System

Herein we propose a multiple injection and recovery well system strategically operated for freshwater storage in a brackish aquifer. With the system we call aquifer storage transfer and recovery (ASTR) by using four injection and two production wells, we are capable of achieving both high recovery efficiency of injected freshwater and attenuation of contaminants through adequately long residence times and travel distances within the aquifer. The usual aquifer storage and recovery (ASR) scheme, in which a single well is used for injection and recovery, does not warrant consistent treatment of injected water due to the shorter minimum residence times and travel distances. We tested the design and operation of the system over 3 years in a layered heterogeneous limestone aquifer in Salisbury, South Australia. We demonstrate how a combination of detailed aquifer characterization and solute transport modeling can be used to maintain acceptable salinity of recovered water for its intended use along with natural treatment of recharge water. ASTR can be used to reduce treatment costs and take advantage of aquifers with impaired water quality that might locally not be otherwise beneficially used.     

Normative composition and classification of lunar igneous rocks and glasses,I. Lunar igneous rocks

678 major element analyses and all available trace element determinations of lunar rocks with igneous textures were collected from the literature. Rittmann norms were calculated by an ALGOL program. The norm values, grouped according to increasing clinopyroxene contents, were plotted into quartz-plagioclase-orthopyroxene and olivine-plagioclase-orthopyroxene triangles, respectively. The plots indicate that all lunar rocks form a compositional continuum that starts from rocks very high in plagioclase and continues, with increasing clinopyroxene, to plagioclase-poorer and orthopyroxene-richer rocks containing partly quartz, partly olivine.According to apparent clusters in the plots, and taking into account lunar rock types defined by previous authors, the continuum of normative compositions was subdivided into five major rock groups (I to V). The averages of these groups can be characterized by clinopyroxene contents and plagioclase/orthopyroxene ratios (I: 3% cpx, plag/opx = 30; II: 4% cpx, plag/opx = 7; III: 8% cpx, plag/opx = 2; IV: 26% cpx, plag/opx = 0.8; V: 34% cpx, plag/opx = 1.8). According to the contents in K-feldspar, from groups III and V K-rich subgroups were separated. Average contents of major elements and trace elements were calculated for main groups and subgroups.For the normative groups of lunar igneous rocks, names are proposed which conform to the nomenclature of terrestrial rocks.     

Sources and distribution of organic matter in northern Patagonia fjords,Chile (∼44–47°S): A multi-tracer approach for carbon cycling assessment

We investigated the provenance of organic matter in the inner fjord area of northern Patagonia, Chile (～44–47°S), by studying the elemental (organic carbon, total nitrogen), isotopic (δ¹³C, δ¹⁵N), and biomarker (n-alkanoic acids from vascular plant waxes) composition of surface sediments as well as local marine and terrestrial organic matter. Average end-member values of N/C, δ¹³C, and δ¹⁵N from organic matter were 0.127±0.010, ?19.8±0.3‰, and 9.9±0.5‰ for autochthonous (marine) sources and 0.040±0.018, ?29.3±2.1‰, and 0.2±3.0‰ for allochthonous (terrestrial) sources. Using a mixing equation based on these two end-members, we calculated the relative contribution of marine and terrestrial organic carbon from the open ocean to the heads of fjords close to river outlets. The input of marine-derived organic carbon varied widely and accounted for 13–96% (average 61%) of the organic carbon pool of surface sediments. Integrated regional calculations for the inner fjord system of northern Patagonia covered in this study, which encompasses an area of ～4280 km², suggest that carbon accumulation may account for between 2.3 and 7.8×10⁴ ton C yr^?1. This represents a storage capacity of marine-derived carbon between 1.8 and 6.2×10⁴ ton yr^?1, which corresponds to an assimilation rate of CO₂ by marine photosynthesis between 0.06 and 0.23×10⁶ ton yr^?1. This rate suggests that the entire fjord system of Patagonia, which covers an area of ～240,000 km², may represent a potentially important region for the global burial of marine organic matter and the sequestration of atmospheric CO₂.     

Estrogenic Activity and Volume Fraction of Waste Water Origin in Monitoring Wells Along the Santa Cruz River, Arizona

The fate of estrogenic activity in waste water effluent was examined during surface transport and incidental recharge along the Santa Cruz River in Pima County, Arizona. Based on measurement of boron isotopes, the fractional contribution of reclaimed water in surface waters and ground water wells proximate to the river was determined for a contemporary sample set. Estrogenic activity decreased by −60% over the 25 mi length of the river below effluent discharge points in Tucson. In ground water samples obtained from monitoring wells that are proximate to the Santa Cruz River, both dissolved organic carbon ( p = 0.0003) and estrogenic activity ( p = 3 × 10⁻⁶) were highly correlated to fractional waste water content. Results indicate that proximate ground water quality is sensitive to incidental recharge of reclaimed water in the Santa Cruz River bed. In a few locations, little attenuation of estrogenic activity was apparent during percolation of effluent in the river channel to well withdrawal points.     

Atmospherically-derived radionuclides as tracers of sediment mixing and accumulation in near-shore marine and lake sediments: Evidence from7Be,210Pb,and239,240Pu

Cosmogenic⁷Be(t_1/2 = 53.3days) has been used to estimate particle-mixing rates in the upper layers of lacustrine and near-shore marine sediments. Excess²¹⁰Pb and/or^239,240Pu have provided limits on rates of sediment accumulation in these environments and indices of the efficiency of the sediments as collectors of reactive nuclides over longer time scale.In sediment cores from Long Island Sound (marine) and Lake Whitney (fresh-water)⁷Be was measurable in the top 2–3 cm. Diffusion-analog particle-mixing coefficients calculated from these data are in the range of 10^?7 cm²/s. For Long Island Sound the coefficients are lower by factors of 3–6 than those estimated from the depth distributions of excess²³⁴Th at the same stations [14]. For Lake Whitney the calculated mixing coefficient is an upper limit because of the possibility of a sampling artifact.Measurements of total (wet + dry) atmospheric deposition of⁷Be in New Haven give an average flux of 0.07 dpm/cm² day during March-November, 1977; this is equivalent to a steady-state inventory of 5.4 dpm/cm² in a perfect collector. Sediment cores from Long Island Sound contain about half this⁷Be inventory, consistent with either a mean residence time for⁷Be in the water column of about one half-life or with post-depositional loss of⁷Be from Long Island Sound sediments. The Lake Whitney cores contain about 5 dpm/cm², much nearer the atmospheric delivery. A higher inventory of⁷Be in fresh-water, as compared to marine, sediments could be due either to a shorter mean residence time for⁷Be in fresh water or to lateral transport processes in the lake or its catchment. High inventories of excess²¹⁰Pb and^239,240Pu in Lake Whitney sediments demonstrate the importance of lateral transport on longer time scales at least.