Coal mining along the Warfield Fault, Mingo County, West Virginia: a tale of ups and downs

Mine development along a 15-mile (24 km) section of the Warfield Fault in Mingo County, West Virginia has broadened the geological understanding of the fault and its related structures. The fault has been exposed in two new road cuts, one in the northeast-trending segment at Neely Branch and one in the eastern east-trending segment at the head of Marrowbone Creek. Both exposures show a well-defined normal fault with a 45° to 55° N dip, juxtaposing sandstone/shale packages from the roof and the floor of the Coalburg seam. The fault is associated with a thin gouge zone, some drag folding, and parallel jointing. Its trace tends to run parallel to the crest of the adjacent Warfield Anticline. Based on underground mine development and detailed core drilling, the vertical offset along the fault plane ranges from a maximum of 240 ft (73 m) in the central part of the area near the structural bend to less than 100 ft (30 m) in western and eastern directions. The fault is located along the relatively steeply dipping (locally in excess of 25%) southern limb of the Warfield Anticline, and appears related to a late phase of extension involving folded Pennsylvanian strata. On a regional scale, the lithological variations across the fault do not suggest any appreciable strike-slip component.Underground room and pillar mines in the Coalburg seam north and south of the fault have been greatly impacted by the Warfield structures. Due to the combined (and opposite) effects of the folding and faulting, the northern mines are located up to 400 ft (125 m) higher in elevation than the southern ones. Overland conveyor belts connect mining blocks separated by the fault. The practical mining limit along the steep slopes toward the fault is around 15%. Subsidiary normal faults with offsets in the 5- to 15-ft (1.5–4.5 m) range are fairly common and form major roof control and production hurdles. Overall, the Warfield structures pose an extra challenge to mine development in this part of the Appalachian Coalfields.     

The identifiability of parameters in a water quality model of the Biebrza River, Poland

The identifiability of model parameters of a steady state water quality model of the Biebrza River and the resulting variation in model results was examined by applying the Monte Carlo method which combines calibration, identifiability analysis, uncertainty analysis, and sensitivity analysis. The water quality model simulates the steady state concentration profiles of chloride, phosphate, ammonium, and nitrate as a function of distance along a river. The water quality model with the best combination of parameter values simulates the observed concentrations very well. However, the range of possible modelled concentrations obtained for other more or less equally eligible combinations of parameter values is rather wide. This range in model outcomes reflects possible errors in the model parameters. Discrepancies between the range in model outcomes and the validation data set are only caused by errors in model structure, or (measurement) errors in boundary conditions or input variables. In this sense the validation procedure is a test of model capability, where the effects of calibration errors are filtered out. It is concluded that, despite some slight deviations between model outcome and observations, the model is successful in simulating the spatial pattern of nutrient concentrations in the Biebrza River.     

Rhenium and chalcophile elements in basaltic glasses from Ko’olau and Moloka’i volcanoes: Magmatic outgassing and composition of the Hawaiian plume

The behavior of chalcophile metals in volcanic environments is important for a variety of economic and environmental applications, and for understanding large-scale processes such as crustal recycling into the mantle. In order to better define the behavior of chalcophile metals in ocean island volcanoes, we measured the concentrations of Re, Cd, Bi, Cu, Pb, Zn, Pt, S, and a suite of major elements and lithophile trace elements in moderately evolved (6-7% MgO) tholeiitic glasses from Ko’olau and Moloka’i volcanoes. Correlated variations in the Re, Cd, and S contents of these glasses are consistent with loss of these elements as volatile species during magmatic outgassing. Bismuth also shows a good correlation with S in the Ko’olau glasses, but undegassed glasses from Moloka’i have unexpectedly low Bi contents. Rhenium appears to have been more volatile than either Cd or Bi in these magmas.Undegassed glasses with 880-1400 ppm S have 1.2-1.5 ppb Re and 130-145 ppb Cd. In contrast, outgassed melts with low S (<200 ppm) are depleted in these elements by factors of 2-5. Key ratios such as Re/Yb and Cu/Re are fractionated significantly from mantle values. Copper, Pb, and Pt contents of these glasses show no correlation with S, ruling out segregation of an immiscible magmatic sulfide phase as the cause of these variations. Undegassed Hawaiian tholeiites have Re/Yb ratios significantly higher than those of MORB, and extend to values greater than that of the primitive mantle. Loss of Re during outgassing of ocean island volcanoes, may help resolve the apparent paradox of low Re/Os ratios in ocean island basalts with radiogenic Os isotopic compositions. Plume source regions with Re/Yb ratios greater than that of the primitive mantle may provide at least a partial solution to the “missing Re” problem in which one or more reservoirs with high Re/Yb are required to balance the low Re/Yb of MORB.Lithophile trace element compositions of most Ko’olau and Moloka’i tholeiites are consistent with variable degrees of melting of fertile mantle peridotite. However, light rare earth element (LREE)-enriched glasses have trace element compositions more consistent with a garnet-rich source having a distinctive trace element composition. This provides additional evidence for a unique source component possibly related to recycled oceanic crust contributing to Ko’olau tholeiites.     

Equilibrium interface segregation in the diopside-forsterite system II: Applications of interface enrichment to mantle geochemistry

Segregation of incompatible elements at grain interfaces may have considerable influence on the physical and chemical properties of mantle rocks. Using a recently developed predictive model to estimate the interface enrichment of elements based on their mineral/melt partitioning (Hiraga and Kohlstedt, companion paper), we consider interface enrichment for a simplified model peridotite consisting of olivine, orthopyroxene, and clinopyroxene. Our calculated results reveal the following: (1) Significant amounts of heavy alkali elements and rare gases likely reside at grain-grain interfaces, whereas interface concentrations of less incompatible are less pronounced. (2) The contribution of the chemical components stored at interfaces to whole-rock chemistry strongly depends on mineral mode and, most importantly, on grain size. (3) Grain size reduction resulting from dynamic recrystallization can increase the total storage of highly incompatible elements on grain interfaces and thereby will diminish their concentration in mineral grains. (4) Analysis of Cs concentrations in mantle clinopyroxenes potentially provides estimates of the grain size of mantle rocks. (5) Transport through peridotite will be dominated by diffusion along interfaces rather than through grain interiors for elements less compatible than Lu.     

Chromite crystallization in a multicellular magma flow: Evidence from a chromitite dike in the Oman ophiolite

The investigated chromitite dike is located at the top of an upwelling mantle structure of the Oman ophiolite (Maqsad diapir), in undeformed dunites displaying evidence for magma impregnation and circulation, just below the paleo-ridge axis. The chromitite dike is undeformed, its shape is that of an upward widening tube. It exhibits an internal layering which is roughly perpendicular to the cavity axis and comprises a vertical succession of four main layers showing a graded-bedding. Chromitite magmatic structures are beautifully preserved and result from a progressive crystallization from small euhedral crystals to wide octahedron-shaped nodules; dissolution textures provide evidence for late magmatic desequilibrium; sedimentation structures include flattening of the largest nodules. The silicate matrix comprises poikilitic forsterite and a locally abundant association of primary pargasite and plagioclase and alteration minerals (vesuvianite-chlorite-dolomite); pargasite inclusions are very abundant in the chromite. Chromite composition changes from one layer to the other and from core to rim in the chromite nodules (chromium decreases and titanium increases); Ti contents are generally high (0.4 to 0.8 wt.% TiO₂) with respect to podiform chromites. Platinum-group elements are not abundant but they show a strong fractionation at the scale of the orebody and of the main graded-bedded layers (Pd/Ir ratio varies from 0.5 to 11.5). REE patterns of chromitite parallel to those of gabbros and furthermore display a sea water related hydrothermal alteration (Ce negative anomaly).

The chromitite dike of Maqsad provides evidence for the crystallization of chromitite bodies in subvertical magma conduits below oceanic ridges; it corroborates the model of Cassard et al. (1981) and Lago et al. (1982) concerning the formation of chromitite pods in ophiolites which were later deformed and transposed into the horizontal plane due to the plastic flow prevailing away from the paleo-axial zone. Layering and chromite compositional variations are ascribed to a multicellular convective system segregating various stocks of chromite particles either in the upwelling flow of fresh magma or in the convective cells of fractionated residual magma in the confined part of the cavity. The estimated life-time for the magma influx is very short (<2 months). The parent-magma was probably of MORB-type and already fractionated (Ti-rich and PGE-poor), which is consistent with the strong evidence of magma-peridotite interactions in the core of the Maqsad diapir. Hydrous fluids were present during chromite crystallization (pargasite inclusions) suggesting that fluid-rich melts occur in the upper mantle.     

Atmospheric boundary-layer structure observed during a haze event due to forest-fire smoke

During a haze event in Baltimore, U.S.A. from July 6 to 8, 2002, smoke from forest fires in the Québec region (Canada), degraded air quality and impacted upon local climate, decreasing solar radiation and air temperature. The smoke particles in and above the atmospheric boundary layer (ABL) served as a tracer and provided a unique opportunity to investigate the ABL structure, especially entrainment. Elastic backscatter lidar measurements taken during the haze event distinctly reveal the downward sweeps (or wisps) of smoke-laden air from the free atmosphere into the ABL. Visualisations of mechanisms such as dry convection, the entrainment process, detrainment, coherent entrainment structures, and mixing inside the ABL, are presented. Thermals overshooting at the ABL top are shown to create disturbances in the form of gravity waves in the free atmosphere aloft, as evidenced by a corresponding ripple structure at the bottom of the smoke layer. Lidar data, aerosol ground-based measurements and supporting meteorological data are used to link free atmosphere, mixed-layer and ground-level aerosols. During the peak period of the haze event (July 7, 2002), the correlation between time series of elastic backscatter lidar data within the mixed layer and the scattering coefficient from a nephelometer at ground level was found to be high (R=0.96 for z =324 m, and R=0.89 for z=504 m). Ground-level aerosol concentration was at a maximum about 2 h after the smoke layer intersected with the growing ABL, confirming that the wisps do not initially reach the ground.     

Concentration profiles of particles settling in the neutral and stratified atmospheric boundary layer

An expression for the vertical equilibrium concentration profile of heavy particles, including the effects of canopy on the eddy diffusivity as well as corrections for atmospheric stability, is proposed. This expression is validated against measurements of vertical concentration profiles of corn pollen above a corn field. The fitted theoretical profiles show that particle settling is correctly accounted for. The sensitivity to variations in the turbulent Schmidt number, settling velocity and stability corrections are explicitly characterized. The importance of independent measurements of the surface flux of pollen in future experiments is noted.     

What is the source of baseflow in agriculturally fragmented catchments? Complex groundwater/surface‐water interactions in three tributary catchments of the Wabash River,Indiana, USA

Some conceptual models suggest that baseflow in agriculturally fragmented watersheds may contain little, if any, groundwater. This has critical implications for stream quality and ecosystem functioning. Here, we (a) identify the sources and flowpaths contributing to baseflow using ²²²Rn and ⁸⁷Sr/⁸⁶Sr and (b) quantify mean apparent ages of groundwater and baseflow using multiple isotopic tracers (CFC, SF₆, ³⁶Cl, and ³H) in 4 small (0.08 to 0.64 km²) tributary catchments to the Wabash River in Indiana, USA. ²²²Rn activities and ⁸⁷Sr/⁸⁶Sr ratios indicate that baseflow in 3 catchments is sourced primarily from groundwater; baseflow in the fourth is dominated by a source similar to agricultural run‐off. CFC‐12 data indicate that springs in 1 catchment are discharging significant proportions of water that recharged between 1974 (42 ± 2 years) and 1961 (55 ± 2 years). Those same springs have ³⁶Cl/Cl ratios between 1,381.08 ± 29.37 (×10^?15) and 1,530.64 ± 27.65 (×10^?15) indicating that a substantial proportion of the discharge likely recharged between 1975 (41 years) and 1950 (66 years). Groundwater samples collected from streambed mini‐piezometers in a separate catchment have CFC‐12 concentrations indicating that a large proportion of the recharge occurred between 1948 (68 ± 2 years) and 1950 (66 ± 2 years). Repeat sampling conducted in September 2015 after above‐average summer rainfall did not show significant decreases in mean apparent age. The relatively old ages observed in 3 of the catchments can be explained by geological complexities that are likely present in all 4 catchments, but overwhelmed by flow from the shallow phreatic aquifer in the fourth catchment.     

Lateral extrusion along the Altyn Tagh Fault,Qilian Shan (NE Tibet): insight from a 3D crustal budget

The lithospheric strike‐slip Altyn Tagh Fault has accommodated hundreds of kilometres of displacement between the Qaidam and Tarim blocks since its Eocene reactivation. However, the way the deformation is accommodated in the Qilian Shan and further east remains uncertain. Based on 360 km of north‐eastward migration of the relatively rigid Qaidam block along the Altyn Tagh Fault and 3D isovolumetric balancing of the crustal deformation within the Altyn Tagh Fault–Qilian Shan system, we demonstrate that 250 ± 28 km (43.8–49.4%) of N20E directed crustal shortening and an additional ~250–370 km of eastward motion of the Qilian Shan crust must be accounted for by strike‐slip faulting in the Qilian Shan and crustal thickening in the Qinling area, as well as by extension in the adjoining North China block graben systems.