Three-Dimensional Experimental Testing of a Two-Phase Flow-Modeling Approach for Air Sparging

Air sparging has been used for several years as an in situ technique for removing volatile compounds from contaminated ground water, but few studies have been completed to quantify the extent of remediation. To gain knowledge of the air flow and water behavior around air injection wells, laboratory tests and model simulations were completed at three injection flow rates (62, 187, and 283 lpm) in a cylindrical reactor (diameter - 1.2 m, depth = 0.65 m). Measurements of the air flux distribution were made across the surface of the reactor at 24 monitoring locations, six radial positions equally spaced along two orthogonal transects. Simulations using a multiphase flow model called T2VOC were completed for a homogeneous, axisymmetric configuration. Input parameters were independently measured soil properties. In all the experiments, about 75 percent of the flow injected exited the water table within 30 cm of the sparge well. Predictions with T2VOC showed the same. The averages of four flux measurements at a particular distance from the sparge well compare satisfactorily with T2VOC predictions. Measured flux values at a given radius varied by more than a factor of two, but the averages were consistent between experiments and agreed well with T2VOC simulations. The T2VOC prediction of the radial extent of sparging coincided with the distance out to which air flow from the sparge well could not be detected in the reactor. The sparging pattern was relatively unaffected by the air injection rate over the range of conditions studied. Changes in the injection rate resulted in nearly proportional changes in flux rates.     

A combined IR and XRD study of natural well crystalline goethites (α-FeOOH)

Acta Geochimica - Goethite (α-FeOOH) is one of the most abundant minerals on the Earth surface, occurring in temperate, tropical and equatorial climates. Fe in goethite can be substituted by...     

Chemical fractionation of zinc versus cadmium among other metals nickel, copper and lead in the northern North Sea

Concentrations of dissolved Ni, Cu, Zn, Cd and Pb were measured in water samples collected during a cruise with R.V Pelagia (29-6/14-7-1993) in the northern North Sea and N.E. Atlantic Ocean. At least six depths (0–90 m) were sampled with modified Go-Flo samplers from a rubber zodiac. In the study area, the first 25 m were well mixed and stratification occurred below this depth. The local bloom of Emiliania huxleyi hardly affected the trace metals concentration, except for some removal of Cd as seen from its correlation with nitrate. The mean dissolved concentrations were for Ni (3.66 nM), Cu (1.61 nM), Zn (4.5 nM), Cd (48 pM) and Pb (108 pM). These concentrations are among the lowest reported for the North Sea and are of similar magnitude to those found in the eastern North Atlantic at the same latitude. Zn was the only exception with values 10 times higher compared to those in the Atlantic Ocean, suggesting external inputs, mainly atmospheric and possibly from surrounding land masses. The observed ratio Zn:Cd in the North Sea and estuaries is in between the high ratio 600–900 for continental sources and the low ratio 5–10 for oceanic waters. Latter low ratio is consistent with the 21-fold stronger inorganic complexation of Cd in seawater which, in combination with the preferential biological uptake of Zn, may lead to the observed about hundredfold fractionation of Zn versus Cd in the marine system. Other processes may play a role but would need further investigation. The dissolved Pb values tend to be lower than found before in the North Sea, indicating decreasing inventories due to reduced anthropogenic emissions.     

Gold mineralization in the Mazowe area, Harare-Bindura-Shamva greenstone belt, Zimbabwe: II. Genetic relationships deduced from mineralogical, fluid inclusion and stable isotope studies, and the Sm-Nd isotopic composition of scheelites

In the Mazowe area some 40 km NW of Harare in Zimbabwe, gold mineralization is hosted in a variety of lithologies of the Archean Harare-Bindura-Shamva greenstone belt, in structures related to the late Archean regional D2/3 event. Conspicuous mineralzogical differences exist between the mines; the mainly granodiorite-hosted workings at Mazowe mine are on pyrite-rich reefs, mines of the Bernheim group have metabasalt host rocks and are characterized by arsenopyrite-rich ores, and Stori's Golden Shaft and Alice mine, both in metabasalts, work sulfide-poor quartz veins. In contrast to the mineralogical diversity, near-identical fluid inventories were found at the different mines. Both H₂O-CO₂-CH₄ fluids of low salinity, and highly saline fluids are present and are regarded to indicate fluid mixing during the formation of the deposits. Notably, these fluid compositions in the Mazowe gold field markedly contrast to ore fluids “typical” of Archean mesothermal gold deposits on other cratons. Stable isotope compositions of quartz from the various deposits (δ¹⁸O=10.8 to 13.2‰ SMOW), calcite (δ¹⁸O=9.5 to 11.9‰ SMOW and δ¹³C=−3.2 to −8.0‰ PDB), inclusion water (δD=−28 to −40‰ SMOW) and sulfides (δ³⁴S=1.3 to 3.2‰ CDT) are uniform within the range typical for Archean lode gold deposits worldwide. The fluid and stable isotope compositions support the statement that the mineralization in the Mazowe gold field formed from relatively reduced fluids with a “metamorphic” signature during a single event of gold mineralization. Microthermometric data further indicate that the deposits formed in the PT range of 1.65–2.3 kbar and 250–380 °C. Ages obtained by using the Sm/Nd and Rb/Sr isotope systems on scheelites are 2604 ± 84 Ma for the mineralization at Stori's Golden Shaft mine, and 2.40 ± 0.20 Ga for Mazowe mine. The Archean age at Stori's is regarded as close to the true age of gold mineralization in the area, whereas the Proterozoic age at Mazowe mine probably reflects later resetting. Received: 30 September 1998 / Accepted: 17 August 1999     

Platinum group elements and gold in ferromanganese crusts from Afanasiy-Nikitin seamount,equatorial Indian Ocean: Sources and fractionation

The major element relationships in ferromanganese (Fe-Mn) crusts from Afanasiy-Nikitin seamount (ANS), eastern equatorial Indian Ocean, appear to be atypical. High positive correlations (r = 0.99) between Mn/Co and Fe/Co ratios, and lack of correlation of those ratios with Co, Ce, and Ce/Co, indicate that the ANS Fe-Mn crusts are distinct from Pacific seamount Fe-Mn crusts, and reflect region-specific chemical characteristics. The platinum group elements (PGE: Ir, Ru, Rh, Pt, and Pd) and Au in ANS Fe-Mn crusts are derived from seawater and are mainly of terrestrial origin, with a minor cosmogenic component. The Ru/Rh (0.5–2) and Pt/Ru ratios (7–28) are closely comparable to ratios in continental basalts, whereas Pd/Ir ratios exhibit values (<2) similar to CI-chondrite (∼1). The chondrite-normalized PGE patterns are similar to those of igneous rocks, except that Pd is relatively depleted. The water depth of Fe-Mn crust formation appears to have a first-order control on both major element and PGE enrichments. These relationships are defined statistically by significant (r > 0.75) correlations between water depth and Mn/Co, Fe/Co, Ce/Co, Co, and the PGEs. Fractionation of the PGE-Au from seawater during colloidal precipitation of the major-oxide phases is indicated by well-defined linear positive correlations (r > 0.8) of Co and Ce with Ir, Ru, Rh, and Pt; Au/Co with Mn/Co; and by weak or no correlations of Pd with water depth, Co-normalized major-element ratios, and with the other PGE (r < 0.5). The strong enrichment of Pt (up to 1 ppm) relative to the other PGE and its positive correlations with Ce and Co demonstrate a common link for the high concentrations of all three elements, which likely involves an oxidation reaction on the Mn-oxide and Fe-oxyhydroxide surfaces. The documented fractionation of PGE-Au and their positive association with redox sensitive Co and Ce may have applications in reconstructing past-ocean redox conditions and water masses.     

The local impacts of climate change in the Ferlo, Western Sahel

Recent increases in the accuracy of climate models have enhanced the possibilities for analyzing the impacts of climate change on society. This paper explores how the local, economic impacts of climate change can be modeled for a specific eco-region, the Western Sahel. The people in the Sahel are highly dependent on their natural resource base, and these resources are highly vulnerable to climate change, in particular to changes in rainfall. Climate models project substantial changes in rainfall in the Sahel in the coming 50 years, with most models predicting a reduction in rainfall. To connect climate change to changes in ecosystem productivity and local income, we construct an ecological–economic model that incorporates rangeland dynamics, grazing and livestock prices. The model shows that decreased rainfall in the Sahel will considerably reduce local incomes, in particular if combined with increases in rainfall variability. Adaptation to these climate change projections is possible if reductions in rainfall are followed by destocking to reach efficient grazing levels. However, while such a strategy is optimal from the perspective of society, the stocking rate is determined by individual pastoralists that face few incentives to destock.     

The molecular mechanism of Mo isotope fractionation during adsorption to birnessite

Fractionation of Mo isotopes during adsorption to manganese oxides is a primary control on the global ocean Mo isotope budget. Previous attempts to explain what drives the surprisingly large isotope effect δ^97/95Mo_dissolved-δ^97/95Mo_adsorbed=1.8‰ have not successfully resolved the fractionation mechanism. New evidence from extended X-ray absorption fine structure analysis and density functional theory suggests that Mo forms a polymolybdate complex on the surfaces of experimental and natural samples. Mo in this polynuclear structure is in distorted octahedral coordination, while Mo remaining in solution is predominantly in tetrahedral coordination as . Our results indicate that the difference in coordination environment between dissolved Mo and adsorbed Mo is the cause of isotope fractionation. The molecular mechanism of metal isotope fractionation in this system should enable us to explain and possibly predict metal isotope effects in other systems where transition metals adsorb to mineral surfaces.     

The geology and genesis of the Tarcoola gold deposits,South Australia

The Tarcoola goldfield is located in the Gawler Craton in northwestern Eyre Peninsula, South Australia. The gold deposits are hosted in the Middle Proterozoic Tarcoola Formation, comprised of the fluviatile Peela Coglomerate Member, the shallow marine Fabian Quartzite Member, and the marine Sullivan Shale Member. Mineralization in the goldfield consists of north-northeast to north-northwest trending gold-bearing quartz veins with associated hematite, pyrite, arsenopyrite, sphalerite, chalcopyrite, galena, electrum and gold. Adamellite in contact with the Tarcoola Formation has previously been included in the Middle Proterozoic Hiltaba Suite granitoids, on the basis of an apparent intrusive relationship with the Tarcoola Formation, and the gold-quartz veins were interpreted as being genetically related to the cooling pluton. However, detailed field and petrographic studies have demonstrated that the contact between the Tarcoola Formation and adamellite is a nonconformity. Hence, there is no genetic relationship between the mineralization and the adamellite. Oxygen isotope data indicate that an oreforming fluid, derived from convective circulation of meteoric or seawater, or from formation water, underwent isotope exchange with sediments of the Tarcoola Formation. A magmatic heat source for the hydrothermal system is suggested by the presence of intrusive igneous rocks, including dykes of aplite, quartz monzonite and microdiorite. Sulphur isotope characteristics of the mineralization can be explained by reduction of seawater sulphate or dissolution of disseminated sulphides in the sedimentary sequence. Metals were probably derived from rocks of the Tarcoola Formation. A complex paragenetic sequence involved deposition of minerals in several stages separated by episodes of fracturing. Fluid inclusions in quartz and fluorite show that deposition took place over a temperature range of about 340° to 110°C from a low salinity fluid. Analyses of chlorite coexisting with sulphide minerals suggest deposition of sulphides from about 300° to 170°C. Gold was transported as Au(HS) ₂ ^– and deposition appears to have coincided with a sudden decrease in fO₂ at around 260° to 250 °C.     

Pliocene clays from Aegina (Greece): Reference material for chemical provenance studies on bronze age pottery from the Island

Normally, the use of clays as reference materials in chemical provenance studies of ancient ceramics is complicated due to the original clay paste processing. The primary mixing and/or refining of raw materials during pottery production makes a straightforward comparison of archaeological ceramics with extant geological materials difficult if not impossible in many cases. However, in the case of Pliocene clays from Aegina (Greece), which were examined chemically and mineralogically and compared with Bronze Age pottery produced on the island, a successful exception can be presented. The chemical composition of a large group of Aeginetan pottery resembles the chemical composition of clays from a deposit in close vicinity to the main Bronze Age settlement of the island. Clays from specific outcrops exhibit considerable chemical and mineralogical homogeneity, and the suitability of those clays for pottery production apparently made substantial clay paste processing unnecessary. © 2004 Wiley Periodicals, Inc.