Dissolved metals and associated constituents in abandoned coal-mine discharges,Pennsylvania, USA. Part 1: Constituent quantities and correlations

Complete hydrochemical data are rarely reported for coal-mine discharges (CMD). This report summarizes major and trace-element concentrations and loadings for CMD at 140 abandoned mines in the Anthracite and Bituminous Coalfields of Pennsylvania. Clean-sampling and low-level analytical methods were used in 1999 to collect data that could be useful to determine potential environmental effects, remediation strategies, and quantities of valuable constituents. A subset of 10 sites was resampled in 2003 to analyze both the CMD and associated ochreous precipitates; the hydrochemical data were similar in 2003 and 1999. In 1999, the flow at the 140 CMD sites ranged from 0.028 to 2210 L s⁻¹, with a median of 18.4 L s⁻¹. The pH ranged from 2.7 to 7.3; concentrations (range in mg/L) of dissolved (0.45-μm pore-size filter) SO₄ (34–2000), Fe (0.046–512), Mn (0.019–74), and Al (0.007–108) varied widely. Predominant metalloid elements were Si (2.7–31.3 mg L⁻¹), B (<1–260 μg L⁻¹), Ge (<0.01–0.57 μg L⁻¹), and As (<0.03–64 μg L⁻¹). The most abundant trace metals, in order of median concentrations (range in μg/L), were Zn (0.6–10,000), Ni (2.6–3200), Co (0.27–3100), Ti (0.65–28), Cu (0.4–190), Cr (<0.5–72), Pb (<0.05–11) and Cd (<0.01–16). Gold was detected at concentrations greater than 0.0005 μg L⁻¹ in 97% of the samples, with a maximum of 0.0175 μg L⁻¹. No samples had detectable concentrations of Hg, Os or Pt, and less than half of the samples had detectable Pd, Ag, Ru, Ta, Nb, Re or Sn. Predominant rare-earth elements, in order of median concentrations (range in μg/L), were Y (0.11–530), Ce (0.01–370), Sc (1.0–36), Nd (0.006–260), La (0.005–140), Gd (0.005–110), Dy (0.002–99) and Sm (<0.005–79). Although dissolved Fe was not correlated with pH, concentrations of Al, Mn, most trace metals, and rare earths were negatively correlated with pH, consistent with solubility or sorption controls. In contrast, As was positively correlated with pH.     

Geochemical controls on lead concentrations in stream water and sediments

The equilibrium distribution of lead in solution and adsorbed on cation exchange sites in sediment theoretically may be calculated from equations representing selectivities of substrate for lead over H⁺, Ca²⁺ and Na⁺, and the stabilities of lead solute species. Such calculations include consideration of total concentrations of major ions, cation exchange capacity (CEC) of substrate, and pH, at values expected in various natural systems. Measurements of CEC and selectivity coefficients were made for synthetic halloysite, a finely divided amorphous 1:1 clay prepared by precipitation from a mixture of solutions of aluminum and silica. Where suspended sediment having the same properties is present in concentrations of 10-1,000 mg/1 at pH 6–8, more than 90% of the lead present can be adsorbed on sediment surfaces. The cation exchange behavior of lead and other minor cationic species in natural systems could be predicted by this type of model if enough other supporting information were available. Information of the type needed describing natural stream sediments, however, is presently inadequate for accurate predictions.     

Dissolved and particulate organic carbon in the North Inlet estuary,South Carolina: What controls their concentrations?

Water samples have been taken daily at 1030 EST from three locations within North Inlet (South Carolina) since June of 1980 in order to evaluate the tidal, seasonal, and eventually annual variability in carbon concentrations within this system and generate hypotheses explaining the observed trends. Dissolved organic carbon (DOC) concentrations within North Inlet (South Carolina) vary inversely with salinity (r²=0.65), suggesting the main source of DOC in North Inlet is freshwater entering from the adjacent forested watershed. This assertion is supported by an observed decrease of tidal water salinity with the onset of streamflow. DOC variability is also associated with (1) groundwater advection and/or runoff and seepage from the marsh surface; (2) removal from tidal water via either physical sorption or biological uptake; (3) sampling location; and (4) origin of water mass. Particulate organic carbon (POC) concentrations vary seasonally, higher values found during the summer. POC variability is controlled by a series of physical and biological factors. Evidence suggests that in the smaller tidal creeks, POC concentrations are associated with (1) rain events scouring the marsh surface, (2) phytoplankton concentrations varying as a function of tidal stage, and (3) removal of particulate material from the marsh surface on the ebb tide. In the larger tidal creeks tidal water velocity appears to be the main factor influencing POC values.     

Sulfide oxidation and distribution of metals near abandoned copper mines in coastal environments,Prince William Sound,Alaska, USA

The oxidation of sulfide-rich rocks, mostly leftover debris from Cu mining in the early 20th century, is contributing to metal contamination of local coastal environments in Prince William Sound, Alaska. Analyses of sulfide, water, sediment, precipitate and biological samples from the Beatson, Ellamar, and Threeman mine sites show that acidic surface waters generated from sulfide weathering are pathways for redistribution of environmentally important elements into and beyond the intertidal zone at each site. Volcanogenic massive sulfide deposits composed of pyrrhotite and (or) pyrite + chalcopyrite + sphalerite with subordinate galena, arsenopyrite, and cobaltite represent potent sources of Cu, Zn, Pb, As, Co, Cd, and Hg. The resistance to oxidation among the major sulfides increases in the order pyrrhotite ? sphalerite < chalcopyrite ? pyrite; thus, pyrrhotite-rich rocks are typically more oxidized than those dominated by pyrite. The pervasive alteration of pyrrhotite begins with rim replacement by marcasite followed by replacement of the core by sulfur, Fe sulfate, and Fe–Al sulfate. The oxi dation of chalcopyrite and pyrite involves an encroachment by colloform Fe oxyhydroxides at grain margins and along crosscutting cracks that gradually consumes the entire grain. The complete oxidation of sulfide-rich samples results in a porous aggregate of goethite, lepidocrocite and amorphous Fe-oxyhydroxide enclosing hydrothermal and sedimentary silicates. An inverse correlation between pH and metal concentrations is evident in water data from all three sites. Among all waters sampled, pore waters from Ellamar beach gravels have the lowest pH (∼3) and highest concentrations of base metals (to ∼25,000 μg/L), which result from oxidation of abundant sulfide-rich debris in the sediment. High levels of dissolved Hg (to 4100 ng/L) in the pore waters probably result from oxidation of sphalerite-rich rocks. The low-pH and high concentrations of dissolved Fe, Al, and SO₄ are conducive to precipitation of interstitial jarosite in the intertidal gravels. Although pore waters from the intertidal zone at the Threeman mine site have circumneutral pH values, small amounts of dissolved Fe²⁺ in the pore waters are oxidized during mixing with seawater, resulting in precipitation of Fe-oxyhydroxide flocs along the beach–seawater interface. At the Beatson site, surface waters funneled through the underground mine workings and discharged across the waste dumps have near-neutral pH (6.7–7.3) and a relatively small base-metal load; however, these streams probably play a role in the physical transport of metalliferous particulates into intertidal and offshore areas during storm events. Somewhat more acidic fluids, to pH 5.3, occur in stagnant seeps and small streams emerging from the Beatson waste dumps. Amorphous Fe precipitates in stagnant waters at Beatson have high Cu (5.2 wt%) and Zn (2.3 wt%) concentrations that probably reflect adsorption onto the extremely high surface area of colloidal particles. Conversely, crystalline precipitates composed of ferrihydrite and schwertmannite that formed in the active flow of small streams have lower metal contents, which are attributed to their smaller surface area and, therefore, fewer reactive sorption sites. Seeps containing precipitates with high metal contents may contribute contaminants to the marine environment during storm-induced periods of high runoff. Preliminary chemical data for mussels (Mytilus edulis) collected from Beatson, Ellamar, and Threeman indicate that bioaccumulation of base metals is occurring in the marine environment at all three sites.     

Geochemistry and stable isotope investigation of acid mine drainage associated with abandoned coal mines in central Montana,USA

The Great Falls-Lewistown Coal Field (GFLCF) in central Montana contains over 400 abandoned underground coal mines, many of which are discharging acidic water with serious environmental consequences. Areas of the mines that are completely submerged by groundwater have circum-neutral pH and relatively low concentrations of metals, whereas areas that are only partially flooded or freely draining have acidic pH (< 3) and high concentrations of metals. The pH of the mine drains either decreases or increases after discharging to the surface, depending on the initial ratio of acidity (mainly Al and Fe²⁺) to alkalinity (mainly HCO₃^?). In acidic, Fe-rich waters, oxidation of Fe²⁺ after exposure to air is microbially catalyzed and follows zero-order kinetics, with computed rate constants falling in the range of 0.97 to 1.25 mmol L^? 1 h^? 1. In contrast, Fe²⁺ oxidation in near-neutral pH waters appears to be first-order with respect to Fe²⁺ concentration, although insufficient data were collected to constrain the rate law expression. Rates of Fe²⁺ oxidation in the field are dependent on temperature such that lower Fe²⁺ concentrations were measured in down-gradient waters during the day, and higher concentrations at night. Diel cycles in dissolved concentrations of Zn and other trace metals (Mn, Ni) were also noted for down-gradient waters that were net alkaline, but not in the acidic drains.The coal seams of the GFLCF and overlying Cretaceous sandstones form a perched aquifer that lies ~ 50 m above the regional water table situated in the underlying Madison Limestone. The δD and δ¹⁸O values of flooded mine waters suggest local derivation from meteoric water that has been partially evaporated in agricultural soils overlying the coal mines. The S and O isotopic composition of dissolved sulfate in the low pH mine drains is consistent with oxidation of biogenic pyrite in coal under aerated conditions. A clear distinction exists between the isotopic composition of sulfate in the acid mine waters and sulfate in the adjacent sedimentary aquifers, making it theoretically possible to determine if acid drainage from the coal mines has leaked into the underlying Madison aquifer.     

Diurnal variations in,and influences on,concentrations of particulate and dissolved arsenic and metals in the mildly alkaline Wallkill River,New Jersey,USA

Diurnal variations in particulate and dissolved As and metal concentrations were observed in mildly alkaline water from a wetlands site on the Wallkill River in northwestern New Jersey. The site, underlain by glacial sediments over dolomite bedrock, is 10 km downstream from a mined area of the Franklin Marble, host to Zn ores, also As and Mn minerals. In mid-September 2005, maxima and minima in dissolved-oxygen-concentration and pH, typically caused by photosynthesis and respiration, occurred at 2000 and 0800 hours. Concentrations of dissolved As (1.52–1.95 μg/L) peaked at dusk (2000 hours), whereas dissolved Mn and Zn concentrations (76.5–96.9 and 8.55–12.8 μg/L, respectively) were lowest at dusk and peaked at 1000 hours. These opposing cycles probably reflect sorption and desorption of As (an anion), and Mn and Zn (cations) as pH varied throughout the 24-h period. Doubly-peaked cycles of B, Cl, SO₄, and nutrients also were observed; these may result from upstream discharges of septic-system effluent. Both recoverable amd particulate Al, Fe, Mn, and Zn concentrations peaked between 0200 and 0600 hours. The particulate metals cycle, with perturbations at 0400 hours, may be influenced by biological activity.     

Stratigraphic and geochemical controls on naturally occurring arsenic in groundwater,eastern Wisconsin,USA

High arsenic concentrations (up to 12,000 7g/L) have been measured in groundwater from a confined sandstone aquifer in eastern Wisconsin. The main arsenic source is a sulfide-bearing secondary cement horizon (SCH) that has variable thickness, morphology, and arsenic concentrations. Arsenic occurs in pyrite and marcasite as well as in iron oxyhydroxides but not as a separate arsenopyrite phase. Nearly identical sulfur isotopic signatures in pyrite and dissolved sulfate and the correlation between dissolved sulfate, iron, and arsenic concentrations suggest that sulfide oxidation is the dominant process controlling arsenic release to groundwater. However, arsenic-bearing oxyhydroxides can potentially provide another arsenic source if reducing conditions develop or if they are transported as colloids in the aquifer. Analysis of well data indicates that the intersection of the SCH with static water levels measured in residential wells is strongly correlated with high concentrations of arsenic in groundwater. Field and laboratory data suggest that the most severe arsenic contamination is caused by localized borehole interactions of air, water, and sulfides. Although arsenic contamination is caused by oxidation of naturally occurring sulfides, it is influenced by water-level fluctuations caused by municipal well pumping or climate changes, which can shift geographic areas in which contamination occurs. Résumé De fortes concentrations en arsenic, jusqu'à 12000 7g/L, ont été mesurées dans l'eau souterraine d'un aquifère gréseux captif, dans l'est du Wisconsin. La principale source d'arsenic est un horizon à cimentation secondaire (SCH) comportant des sulfures, dont l'épaisseur, la morphologie et les concentrations en arsenic sont variables. L'arsenic est présent dans la pyrite et dans la marcassite, de même que dans des oxy-hydroxydes de fer, mais non pas dans une phase séparée d'arsénopyrite. Les signatures isotopiques du soufre presque identiques dans la pyrite et dans les sulfates dissous et la corrélation entre les concentrations en sulfates, en fer et en arsenic dissous laissent penser que l'oxydation des sulfures est le processus dominant contrôlant la libération de l'arsenic dans les eaux souterraines. Cependant, les oxy-hydroxydes contenant de l'arsenic sont susceptibles d'être une autre source d'arsenic si des conditions réductrices apparaissent ou s'ils sont transportés dans l'aquifère sous forme de colloïdes. L'analyse des données provenant de puits montre que l'intersection entre le SCH et les niveaux statiques des puits domestiques est fortement corrélée à de fortes concentrations en arsenic dans les eaux souterraines. Des données de terrain et de laboratoire conduisent à penser que la contamination en arsenic la plus forte est causée par l'interaction localisée aux forages entre l'air, l'eau et les sulfures. Bien que la contamination en arsenic soit causée par l'oxydation de sulfures présents naturellement, elle est influencée par les fluctuations du niveau piézométrique causées par les pompages du captage municipal ou par les variations climatiques, ce qui peut conduire au déplacement des zones géographiques où se produisent les contaminations. Resumen Se han medido concentraciones de arsénico muy altas (de hasta 12000 7g/L) en las aguas subterráneas de un acuífero confinado, en areniscas, localizado en la parte oriental de Wisconsin (EEUU). La fuente principal de arsénico es un horizonte de cementación secundaria (SCH) con un alto contenido en sulfuros, y con una gran variabilidad en espesor, morfología y concentraciones de As. El arsénico aparece en piritas y marcasitas, además de en oxihidróxidos de hierro, pero no como una fase independiente de arsenopiritas. El hecho que la marca isotópica de piritas y sulfatos disueltos sea muy similar, y que exista una gran correlación entre las concentraciones de sulfato disuelto, hierro y arsénico sugiere que la oxidación de sulfuros es el proceso que controla la aportación de arsénico al agua subterránea. Sin embargo, los oxihidróxidos con alto contenido en arsénico podrían suponer otra fuente de arsénico si se llegaran a desarrollar condiciones reductoras o si se transportaran como coloides por el acuífero. De los datos procedentes de pozos, se ve una fuerte correlación entre la presencia de altas concentraciones de As en el agua y que el nivel freático intersecte el SCH. Los datos de campo y de laboratorio indican que los puntos con mayor contaminación de arsénico son debidos a interacciones de carácter local y en los propios pozos entre aire, agua y sulfuros. Aunque la contaminación por As está causada por la oxidación de sulfuros presentes de manera natural, también está muy influenciada por las fluctuaciones en los niveles freáticos causadas por bombeos o cambios climáticos.     

Temperature–time paths from phosphate accessory phase paragenesis in the Honey Brook Upland and associated cover sequence, SE Pennsylvania, USA

Analysis of monazite-bearing lithologies from the Precambrian Honey Brook Upland (HBU) and overlying metasedimentary Paleozoic Chester Valley Sequence (CVS) (SE PA, USA) reveals overprinting of primary major and accessory phase parageneses by texturally and compositionally disparate secondary accessory phase parageneses. Two-pyroxene temperatures of 915–945 °C for reconstituted pyroxene reflect emplacement temperatures of felsic plutonic rocks (opdalite, charnockite) prior to Mesoproterozoic metamorphism. Monazite in metavolcanic felsic gneiss yields three age domains at 1009 ± 4 Ma (2 s.e.), 965 ± 6, and 876 ± 10 Ma. The first two domains record metamorphism of the HBU after anorthosite intrusion; peak monazite–xenotime temperatures for the monazite core domain are 700 °C, and high Th/U values in the second (overgrowth) age domain likely reflect a second high-T monazite growth episode. Formation of cummingtonite coronas on orthopyroxene in opdalite constrains maximum 1010 Ma metamorphic temperatures in the “granulite-facies” terrane to 730–740 °C. Evidence of increased Cl fluid activity in the 965 Ma metamorphism includes higher Cl content of matrix apatite relative to garnet-included apatite (metavolcanics), and Cl-bearing K-hornblende succeeding cummingtonite in coronal overgrowths (opdalite). Extreme monazite Th/U values (75–250) in the rim domain suggest growth during low-T hydrothermal alteration. In the opdalite, secondary singe-grain monazite and monazite + xenotime metasomites in apatite yield ages of 714 ± 24 and 586 ± 88 Ma, temperatures of 325–425 °C, and are interpreted to reflect thermal disturbances associated with late Proterozoic plutonic and volcanic activity in the Upland. This thermal disturbance may be recorded by Rb–Sr age of 567 Ma for biotite from a HBU gneiss. Monazite age domains in metaquartzite (378 ± 28, 272 ± 44 Ma) suggest that low-grade metamorphism (260–320 °C, Mnz–Xno thermometry) of the CVS is not a result of Taconian orogenesis.     

美国内华达卡林金矿之含金FeS2微晶中不可见金的TEM研究和地球化学模型

透射电子显微术的研究表明,美国内华达州卡林金矿中环绕黄铁矿大 晶体的Fe的硫 化物微晶乃是白铁矿。该白铁矿含Au和As,并在其中有纳米尺度的似带状区。相对于邻区 而言,似带状区相对富As。因而提出：似带状区还相对富晶格金。根据所得出的方解石中三 价阳离子的分配系数方程认为,Au3＋阳离子是在白铁矿的非平衡(快速)结晶 作用期间,从白铁矿－溶液界面上被结合到细粒白铁矿中去的。Au3＋在白铁矿中的 配分是由非平衡分布系数(Kd')所控制的。然而,由于Au 3＋的平衡分 配系数(Kd)小,故通过平衡(缓慢)结晶作用形成的黄铁矿并不将Au 3 ＋结合到晶体中去。早期形成的细粒晶体的再结晶作用则将把REE和Au从晶体中迁移走。 相对于正常的白铁矿结构而言,较大的Au3＋和Au＋阳离子结合进入到白铁矿晶格 中,可引起局部的结构畸变,从而表现为似带状的特征。     

Mercury dynamics in sulfide-rich sediments: Geochemical influence on contaminant mobilization within the Penobscot River estuary, Maine, USA

Research concerning the fate and biogeochemical cycling of mercury (Hg) within coastal ecosystems has suggested that microbially mediated diagenetic processes control Hg mobilization and that ligands with strong affinity for Hg, such as dissolved inorganic sulfide (S(-II)) and dissolved organic matter (DOM), control Hg partitioning between the dissolved and particulate phases. We have studied total Hg cycling in the sediments of the Penobscot River estuary using a combination of equilibrium porewater samplers and kinetic modeling. The Penobscot estuary has been subject to Hg contamination from multiple industries including a recently closed chlor-alkali production facility. The Hg concentration within the estuary surface sediments ranges from 1.25 to 27.5 nmol Hg g⁻¹ sediment and displays an association with sediment organic matter and a concentration maximum within 3 cm of the sediment-water interface (SWI). Porewater profiles for the Penobscot estuary are divisible into three kinetically discrete intervals with respect to Hg dynamics. Beginning at depth in the sediment and moving upward toward the SWI we have defined: (1) a zone of net Hg solubilization at depth, with a zero-order net Hg production rate , (2) a zone of net Hg consumption within the zone dominated by FeS_(s) precipitation with , and (3) a zone of net diffusive transfer within the vicinity of the SWI. Zone 1 is characterized by dissolved S(-II) concentrations ranging from 400 to 500 μM. Equilibrium modeling in this zone suggests that inorganic S(-II) plays the dominant role in both mobilization of sediment-bound Hg and complexation of dissolved Hg. In zone 2, FeS_(s) precipitation occurs concomitant with Hg consumption. Net transfer within zone 3 is consistent with the potential for ligand-mediated Hg efflux across the SWI. S(-II)-mediated Hg mobilization at depth in Penobscot estuary sediments suggests a broadening of the depth interval over which biogeochemical Hg cycling must be examined. Our results also show that, while estuary sediments act as a net sink for particulate Hg inputs, they may also function for a considerable time interval as a source of dissolved Hg.     

Critical shallow and deep hydrologic conditions associated with widespread landslides during a series of storms between February and April 2018 in Pittsburgh and vicinity,western Pennsylvania,USA

The potential for widespread landslides is generally increased when extraordinary wet periods occur during times of elevated subsurface hydrologic conditions. A series of storms in early 2018 in Pittsburgh, Pennsylvania, overlapped with a period of increased shallow soil moisture and rising bedrock groundwater levels resulting from seasonally diminished evapotranspiration and induced widespread landslides in the region. Most of the landslides were shallow slope failures in colluvium, landslide deposits, and/or fill. However, deep-seated landslide activity also occurred and corresponded with record cumulative precipitation from late February to April and bedrock groundwater levels rising to an annual high. Landslides blocked or damaged roads, adversely affected multiple houses, disrupted electrical service, crushed vehicles, and resulted in considerable economic losses. The initial landslides occurred during or immediately after a rare period of three successive days of heavy rain that began on February 14. Subsequent landslides between late February and April were induced by multiday storms with smaller rainfall totals. As shallow soil moisture at a monitoring site rose above a volumetric water content of 32%, the mean rainfall intensities necessary to induce slope failure in colluvium and other surficial deposits decreased. Deep-seated landslide movement occurred in the region mostly when the groundwater level in a bedrock observation well was shallower than 1.7 m. The availability of hydrologic and landslide movement monitoring data during this extraordinary series of storms highlighted the evolution of the landslide hazard with changing moisture conditions and yielded insights into potential hydrologic criteria for anticipating future widespread landslides in the region.

     

Hydrogeologic controls on groundwater recharge and salinization: a geochemical analysis of the northern Hueco Bolson aquifer, Texas, USA

Identification of hydrogeologic controls on groundwater flowpaths, recharge, and salinization is often critical to the management of limited arid groundwater resources. One approach to identifying these mechanisms is a combined analysis of hydrogeologic and hydrochemical data to develop a comprehensive conceptual model of a groundwater basin. To demonstrate this technique, water samples were collected from 33 discrete vertical zone test holes in the Hueco Bolson aquifer, located within the Trans-Pecos Texas region and the primary water resource for El Paso, Texas, USA and Juárez, Mexico. These samples were analyzed for a suite of geochemical tracers and the data evaluated in light of basin hydrogeology. On the basis of δ²H and δ¹⁸O data, two regional recharge sources were recognized, one originating from western mountain-fronts and one from through-flow of the adjacent Tularosa aquifer. Chloride concentrations were strongly correlated with lithologic formations and both Cl/Br and ³⁶Cl ratios suggested the primary chloride source is halite dissolution within a specific lithologic unit. In contrast, sulfur isotopes indicated that most sulfate originates from Tularosa basin Permian gypsum sources. These results yielded a more comprehensive conceptual model of the basin, which suggested that chloride salinization of wells is the result of upconing of waters from the Fort Hancock formation.     

Depositional framework and controls on mixed carbonate-siliciclastic gravity flows: Pennsylvanian-Permian shelf to basin transect, south-western Great Basin, USA

Mixed carbonate-siliciclastic sediment gravity flow deposits of Late Pennsylvanian to Early Permian age are exposed in the Death Valley - Owens Valley region of east-central California. The Mexican Spring unit constitutes the upper part of the Keeler Canyon Formation and is characterized by turbidites, debris flow deposits and megabreccias, all of mixed carbonate-siliciclastic composition. The mixed composition of the Keeler Canyon Formation provides an opportunity to link facies architecture to controls on depositional system development. Depositional relationships indicate that the deposits represent a non-channellized base of slope carbonate apron system with inner, outer and basinal facies associations. These gravity flow deposits are characterized by repeated stacked, small scale (<15 m) coarsening and thickening upward cycles with superimposed medium scale (>100 m) coarsening and thickening upward cycles. Contemporaneous outer shelf and upper slope deposits of the Tippipah Limestone are exposed at Syncline Ridge on the Nevada Test Site. The deposits consist of carbonate buildups directly overlain by cross bedded, quartz-rich sandstone and conglomerate which filled channels that traversed across the previously existing carbonate shelf. Detritus was transported to the west, down the upper slope by gully systems that fed the temporally persistent base of slope apron of the upper part of the Keeler Canyon Formation. This style of deposition differs from point-sourced siliciclastic submarine fan depositional systems. However, the Keeler Canyon system has lithofacies similar to some sandy siliciclastic turbidite systems, such as the delta-fed submarine ramp facies model, which is a line-sourced, shelf-fed system that is not supply limited. The mixed clastic apron systems of the Keeler Canyon Formation differ from classical carbonate aprons in that the former is characterized by an abundance of sedimentary cycles. Controls on the development of these cycles and of the facies distribution may have resulted from changes in type and rate of sediment supply, relative sea level changes and/or tectonic events. Interpretation of the data is focused on relative changes in sea level as the most significant control on development of the depositional system. Relative sea level changes serve two important functions: (1) they provide a mechanism for bringing coarse siliciclastic and bioclastic grains together on the outer shelf, and (2) shelf margin collapse may be initiated during relative lowstands allowing for transport of the sediment to the deep basin and development of deep basinal cycles. Therefore, an abundance of mixed clastic gravity flow deposits such as these in the rock record may be an indicator of periods of high frequency changes in relative sea level, which is a characteristic of Late Palaeozoic sea level history.     

Critical metals in the critical zone: controls,resources and future prospectivity of regolith-hosted rare earth elements

The rare earth elements (REE) are a group of 17 metals that include the lanthanides, Sc and Y, which are critical for many modern technologies including consumer electronics, medicine and communication. One of the major controls on the concentrations of the REE in regolith material (including soils) is the abundance of these elements in the parent material. It is known that REE concentrations are largely inherited from the protolith rather than acquired during pedogenic processes but our understanding of how pedogenesis affects fractionation and accumulation of REE to produce potentially economic deposits of these critical metals is limited. This study provides a review of (1) the biogeochemical controls on REE distribution and mobility during pedogenesis and (2) the potential for REE extraction from regolith material. Factors that control mobilisation of REE during weathering include (1) the initial distribution of the REE in protolith minerals and the resistivity of these phases to weathering, (2) adsorption and absorption of REE to Fe- and Mn oxides, clay minerals and organic matter and (3) variations in pH and Eh conditions. We also discuss the relative importance of biogeochemical controls on REE mobility in soils in southern Australia, where REE concentrations are demonstrated to be largely a function of weathering of REE-enriched protoliths, the sorption of REE to weathering products and the accumulation of resistant minerals in soils.     

Stratigraphic and structural controls on groundwater salinity variations in the Poso Creek Oil Field,Kern County,California, USA

Hydrogeology Journal - Groundwater total dissolved solids (TDS) distribution was mapped with a three-dimensional (3D) model, and it was found that TDS variability is largely controlled by...