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Zinc, copper, and lead geochemistry of oceanic igneous rocks - ridges, islands, and arcs

Variations in the abundances of Zn, Cu, and Pb are found to be useful in identifying tectonic regimes and separating oceanisland basalts into enriched- and depleted-source categories. The average Zn, Cu, and Pb contents of normal mid-ocean ridge basalts (N-MORB) are 84, 70, and 0.35 ppm, respectively. Differences in average Zn contents for various ridges reflect more the varying degrees of differentiation than variations of Zn content in the source rocks. At a Mg# of 70, or Mg# 70 , which is taken to represent primitive MORB, many MORB sequences converge at a Zn content of 58 ± 6 ppm, which is close to the value for primitive mantle (50 ppm) and ordinary chondrites (∼55 ppm). Values of 0.1 to 0.15 ppm Pb in MORB at Mg# 70 , best defined at the superfast-spreading Southern East Pacific Rise, are similar to estimates of Pb in the primitive mantle (0.12 to 0.18 ppm). They also are near the lower end of the range for ordinary chondrites. The very slow spreading Southwest Indian Ocean Ridge has a sequence with higher Pb contents, in addition to a more normal sequence, which has a visual best value of 0.4 ppm Pb at Mg# 70 . With the exception of the Walvis Ridge, Zn and Cu appear to be little affected by proximity to hotspots (i.e., E-MORB); however, Pb contents are higher and average about 0.6 ppm.

International Geology Review

Geochemistry of environmentally sensitive trace elements in Permian coals from the Huainan coalfield, Anhui, China

To study the geochemical characteristics of 11 environmentally sensitive trace elements in the coals of the Permian Period from the Huainan coalfield, Anhui province, China, borehole samples of 336 coals, two partings, and four roof and floor mudstones were collected from mineable coal seams. Major elements and selected trace elements were determined by inductively coupled plasma optical emission spectrometry (ICP-OES), inductively coupled plasma mass spectrometry (ICP-MS), and hydride generation atomic absorption spectrometry (HAAS). The depositional environment, abundances, distribution, and modes of occurrence of trace elements were investigated. Results show that clay and carbonate minerals are the principal inorganic constituents in the coals. A lower deltaic plain, where fluvial channel systems developed successively, was the likely depositional environment of the Permian coals in the Huainan coalfield. All major elements have wider variation ranges than those of Chinese coals except for Mg and Fe. The contents of Cr, Co, Ni, and Se are higher than their averages for Chinese coals and world coals. Vertical variations of trace elements in different formations are not significant except for B and Ba. Certain roof and partings are distinctly higher in trace elements than underlying coal bench samples. The modes of occurrence of trace elements vary in different coal seams as a result of different coal-forming environments. Vanadium, Cr, and Th are associated with aluminosilicate minerals, Ba with carbonate minerals, and Cu, Zn, As, Se, and Pb mainly with sulfide minerals.

Huainan coalfield

Geochemistry of Selected Coal Samples from Sumatra, Kalimantan, Sulawesi, and Papua, Indonesia

Introduction Indonesia is an archipelago of more than 17,000 islands that stretches astride the equator for about 5,200 km in southeast Asia (figure 1) and includes major Cenozoic volcano-plutonic arcs, active volcanoes, and various related onshore and offshore basins. These magmatic arcs have extensive Cu and Au mineralization that has generated much exploration and mining in the last 50 years. Although Au and Ag have been mined in Indonesia for over 1000 years (van Leeuwen, 1994), it was not until the middle of the nineteenth century that the Dutch explored and developed major Sn and minor Au, Ag, Ni, bauxite, and coal resources. The metallogeny of Indonesia includes Au-rich porphyry Cu, porphyry Mo, skarn Cu-Au, sedimentary-rock hosted Au, epithermal Au, laterite Ni, and diamond deposits. For example, the Grasberg deposit in Papua has the world's largest gold reserves and the third-largest copper reserves (Sillitoe, 1994). Coal mining in Indonesia also has had a long history beginning with the initial production in 1849 in the Mahakam coal field near Pengaron, East Kalimantan; in 1891 in the Ombilin area, Sumatra, (van Leeuwen, 1994); and in South Sumatra in 1919 at the Bukit Asam mine (Soehandojo, 1989). Total production from deposits in Sumatra and Kalimantan, from the 19thth century to World War II, amounted to 40 million metric tons (Mt). After World War II, production declined due to various factors including politics and a boom in the world-wide oil economy. Active exploration and increased mining began again in the 1980's mainly through a change in Indonesian government policy of collaboration with foreign companies and the global oil crises (Prijono, 1989). This recent coal revival (van Leeuwen, 1994) has lead Indonesia to become the largest exporter of thermal (steam) coal and the second largest combined thermal and metallurgical (coking) coal exporter in the world market (Fairhead and others, 2006). The exported coal is desirable as it is low sulfur and ash (generally <1 and < 10 wt.%, respectively). Coal mining for both local use and for export has a very strong future in Indonesia although, at present, there are concerns about the strong need for a major revision in mining laws and foreign investment policies (Wahju, 2004; United States Embassy Jakarta, 2004). The World Coal Quality Inventory (WoCQI) program of the U.S. Geological Survey (Tewalt and others, 2005) is a cooperative project with about 50 countries (out of 70 coal-producing countries world-wide). The WoCQI initiative has collected and published extensive coal quality data from the world's largest coal producers and consumers. The important aspects of the WoCQI program are; (1) samples from active mines are collected, (2) the data have a high degree of internal consistency with a broad array of coal quality parameters, and (3) the data are linked to GIS and available through the world-wide-web. The coal quality parameters include proximate and ultimate analysis, sulfur forms, major-, minor-, and trace-element concentrations and various technological tests. This report contains geochemical data from a selected group of Indonesian coal samples from a range of coal types, localities, and ages collected for the WoCQI program.

Open-File Report

Mega-depressions on the Cocos Ridge: Links between volcanism, faults, hydrothermal circulation, and dissolution

High-resolution bathymetry and 3D seismic data along the Cocos Ridge reveal a 245 km 2 field of ∼1 to 4 km in diameter seafloor depressions. The seafloor depressions are part of a two-tiered honeycomb pattern. The lower-tier depressions have steep faults that truncate strata with chaotic internal reflections consistent with sediment collapse into the depression. These extend into a lens shaped interval just above igneous basement. Overlying these depressions is a second broader set with rough seafloor morphology with gently dipping boundaries defined by pinch-out stratigraphic patterns. Drilling results indicate that the lens-shaped zones that host the deeper depressions represent anomalous regions of high porosity, low velocity, and low density within calcareous rich sediment. Analysis of nannofossils from IODP Site U1414 suggests the collapse structures formed during the late Miocene, whereas the younger shallower depressions likely formed between the early Pliocene and the Pliocene-Pleistocene boundary. Geochemical and petrological analysis at Site U1414 suggests that hydrothermal circulation during the late Miocene led to carbonate dissolution and collapse. Following collapse, focused fluid-flow and bottom current scouring resulted in formation of the overlying set of depressions and a honeycomb seafloor morphology. Similar sets of depressions along the Carnegie Ridge to the south support the hypothesis that two-tiered depressions formed in response to processes that occurred broadly across the Panama Basin between the late Miocene and the Pliocene-Pleistocene transition. Geochemical results at Site U1414, combined with geophysical data, suggest this two-tiered system of depressions currently guides ongoing fluid outflow.

Geochemistry, Geophysics, Geosystems

Protracted multipulse emplacement of a post-resurgent pluton: The case of Platoro caldera complex (Southern Rocky Mountain volcanic field, Colorado)

Many eroded calderas expose associated postcollapse plutons, but detailed fieldwork‐supported studies have rarely focused on the internal structure that can contribute to understanding of emplacement dynamics. The Alamosa River monzonite pluton is a postcollapse intrusion at the Platoro caldera complex that erupted six large ignimbrites between 30.2 and 28.8 Ma in the Southern Rocky Mountains volcanic field. Magnetic fabrics in this intrusion indicate the pulsed emplacement of a vertically extensive pluton. The magmatic pulses are documented by three concentric domains of magnetic foliations elongated in ~NE‐SW direction, corresponding to structural trends at the Platoro caldera complex and preexisting regional structures. As no evidence for deformation of wall rocks and the adjacent resurgent block has been identified, we interpret the Alamosa River pluton as a postresurgent intrusion. The space‐opening process involved magmatic stoping and small‐scale magma wedging. New SHRIMP‐RG U/Pb zircon dates (28.98 ±0.18, 27.42 ± 0.35, and 27.32 ± 0.38 Ma) suggest a magmatic lifespan of ~1.7 My for the Alamosa River pluton. Our results indicate that postcaldera magmatism includes pulsed and protracted activity from large intracaldera resurgent plutons to smaller postresurgent stocks and sheeted complexes. As demonstrated by the Alamosa River pluton, some intrusions are emplaced shortly after collapse and resurgence, but postcaldera volcano‐plutonic systems may remain active for several million years or more. We also suggest that subvolcanic magma bodies may be assembled incrementally and that the record of early composite magma lenses preserved as magma wedges are later obliterated by convective flowage and crystallization.

Colorado

Whole-coal versus ash basis in coal geochemistry: a mathematical approach to consistent interpretations

Several standard methods require coal to be ashed prior to geochemical analysis. Researchers, however, are commonly interested in the compositional nature of the whole-coal, not its ash. Coal geochemical data for any given sample can, therefore, be reported in the ash basis on which it is analyzed or the whole-coal basis to which the ash basis data are back calculated. Basic univariate (mean, variance, distribution, etc.) and bivariate (correlation coefficients, etc.) measures of the same suite of samples can be very different depending which reporting basis the researcher uses. These differences are not real, but an artifact resulting from the compositional nature of most geochemical data. The technical term for this artifact is subcompositional incoherence. Since compositional data are forced to a constant sum, such as 100% or 1,000,000 ppm, they possess curvilinear properties which make the Euclidean principles on which most statistical tests rely inappropriate, leading to erroneous results. Applying the isometric logratio (ilr) transformation to compositional data allows them to be represented in Euclidean space and evaluated using traditional tests without fear of producing mathematically inconsistent results. When applied to coal geochemical data, the issues related to differences between the two reporting bases are resolved as demonstrated in this paper using major oxide and trace metal data from the Pennsylvanian-age Pond Creek coal of eastern Kentucky, USA. Following ilr transformation, univariate statistics, such as mean and variance, still differ between the ash basis and whole-coal basis, but in predictable and calculated manners. Further, the stability between two different components, a bivariate measure, is identical, regardless of the reporting basis. The application of ilr transformations addresses both the erroneous results of Euclidean-based measurements on compositional data as well as the inconsistencies observed on coal geochemical data reported on different bases.

International Journal of Coal Geology

N-15 NMR spectra of naturally abundant nitrogen in soil and aquatic natural organic matter samples of the International Humic Substances Society

The naturally abundant nitrogen in soil and aquatic NOM samples from the International Humic Substances Society has been characterized by solid state CP/MAS 15 N NMR. Soil samples include humic and fulvic acids from the Elliot soil, Minnesota Waskish peat and Florida Pahokee peat, as well as the Summit Hill soil humic acid and the Leonardite humic acid. Aquatic samples include Suwannee River humic, fulvic and reverse osmosis isolates, Nordic humic and fulvic acids and Pony Lake fulvic acid. Additionally, Nordic and Suwannee River XAD-4 acids and Suwannee River hydrophobic neutral fractions were analyzed. Similar to literature reports, amide/aminoquinone nitrogens comprised the major peaks in the solid state spectra of the soil humic and fulvic acids, along with heterocyclic and amino sugar/terminal amino acid nitrogens. Spectra of aquatic samples, including the XAD-4 acids, contain resolved heterocyclic nitrogen peaks in addition to the amide nitrogens. The spectrum of the nitrogen enriched, microbially derived Pony Lake, Antarctica fulvic acid, appeared to contain resonances in the region of pyrazine, imine and/or pyridine nitrogens, which have not been observed previously in soil or aquatic humic substances by 15 N NMR. Liquid state 15 N NMR experiments were also recorded on the Elliot soil humic acid and Pony Lake fulvic acid, both to examine the feasibility of the techniques, and to determine whether improvements in resolution over the solid state could be realized. For both samples, polarization transfer (DEPT) and indirect detection ( 1 H- 15 N gHSQC) spectra revealed greater resolution among nitrogens directly bonded to protons. The amide/aminoquinone nitrogens could also be observed by direct detection experiments.

Organic Geochemistry

Geochemistry of trace elements in coals from the Zhuji Mine, Huainan Coalfield, Anhui, China

The abundances of nine major elements and thirty-eight trace elements in 520 samples of low sulfur coals from the Zhuji Mine, Huainan Coalfield, Anhui, China, were determined. Samples were mainly collected from 10 minable coal seams of 29 boreholes during exploration. The B content in coals shows that the influence of brackish water decreased toward the top of coal seams; marine transgression and regression occurred frequently in the Lower Shihezi Formation. A wide range of elemental abundances is found. Weighted means of Na, K, Fe, P, Be, B, Co, Ni, Cr, Se, Sb, Ba, and Bi abundances in Zhuji coals are higher, and the remainder elements are either lower or equal to the average values of elements in coals of northern China. Compared to the Chinese coals, the Zhuji coals are higher in Na, K, Be, B, Cr, Co, Se, Sn, Sb, and Bi, but lower in Ti, P, Li, V and Zn. The Zhuji coals are lower only in S, P, V and Zn than average U.S. and world coals. Potassium, Mg, Ca, Mn, Sr, As, Se, Sb and light rare earth elements (LREE) had a tendency to be enriched in thicker coal seams, whereas Fe, Ti, P, V, Co, Ni, Y, Mo, Pb and heavy rare earth elements (HREE) were inclined to concentrate in thinner coal seams. The enrichment of some elements in the Shanxi or Upper Shihezi Formations is related to their depositional environments. The elements are classified into three groups based on their stratigraphic distributions from coal seams 3 to 11-2, and the characteristics of each group are discussed. Lateral distributions of selected elements are also investigated. The correlation coefficients of elemental abundances with ash content show that the elements may be classified into four groups related to modes of occurrence of these elements. ?? 2009 Elsevier B.V. All rights reserved.

International Journal of Coal Geology

Paleomagnetism and 40Ar/39Ar ages from volcanics extruded during the Matuyama and Brunhes Chrons near McMurdo Sound, Antarctica

Maps of virtual geomagnetic poles derived from international geomagnetic reference field models show large lobes with significant departures from the spin axis. These lobes persist in field models for the last few millenia. The anomalous lobes are associated with observation sites at extreme southerly latitudes. To determine whether these features persist for millions of years, paleomagnetic vector data from the continent of Antarctica are essential. We present here new paleomagnetic vector data and 40 Ar/ 39 Ar ages from lava flows spanning the Brunhes and Matuyama Chrons from the vicinity of McMurdo Sound, Antarctica. Oriented paleomagnetic samples were collected from 50 lava flows by E. Mankinen and A. Cox in the 1965–1966 austral summer season. Preliminary data based largely on the natural remanent magnetization (NRM) directions were published by Mankinen and Cox [1988]. We have performed detailed paleomagnetic investigations of 37 sites with multiple fully oriented core samples to investigate the reliability of results from this unique sample collection. Of these, only one site fails to meet our acceptance criteria for directional data. Seven sites are reversely magnetized. The mean normal and reverse directions are antipodal. The combined mean direction has = 12, = −86, α = 4, κ = 37 and is indistinguishable from that expected from a GAD field. We obtained reproducible absolute paleointensity estimates from 15 lava flows with a mean dipole moment of 49 ZAm 2 and a standard deviation of 28 ZAm 2 . 40 Ar/ 39 Ar age determinations were successfully carried out on samples from 18 of the flows. Our new isotopic ages and paleomagnetic polarities are consistent with the currently accepted geomagnetic reversal timescales.

Geochemistry, Geophysics, Geosystems

Plant phenolics and absorption features in vegetation reflectance spectra near 1.66 μm

Past laboratory and field studies have quantified phenolic substances in vegetative matter from reflectance measurements for understanding plant response to herbivores and insect predation. Past remote sensing studies on phenolics have evaluated crop quality and vegetation patterns caused by bedrock geology and associated variations in soil geochemistry. We examined spectra of pure phenolic compounds, common plant biochemical constituents, dry leaves, fresh leaves, and plant canopies for direct evidence of absorption features attributable to plant phenolics. Using spectral feature analysis with continuum removal, we observed that a narrow feature at 1.66 &mu;m is persistent in spectra of manzanita, sumac, red maple, sugar maple, tea, and other species. This feature was consistent with absorption caused by aromatic C- H bonds in the chemical structure of phenolic compounds and non-hydroxylated aromatics. Because of overlapping absorption by water, the feature was weaker in fresh leaf and canopy spectra compared to dry leaf measurements. Simple linear regressions of feature depth and feature area with polyphenol concentration in tea resulted in high correlations and low errors (% phenol by dry weight) at the dry leaf ( r 2 = 0.95, RMSE = 1.0%, n = 56), fresh leaf ( r 2 = 0.79, RMSE = 2.1%, n = 56), and canopy ( r 2 = 0.78, RMSE = 1.0%, n = 13) levels of measurement. Spectra of leaves, needles, and canopies of big sagebrush and evergreens exhibited a weak absorption feature centered near 1.63 &mu;m, short ward of the phenolic compounds, possibly consistent with terpenes. This study demonstrates that subtle variation in vegetation spectra in the shortwave infrared can directly indicate biochemical constituents and be used to quantify them. Phenolics are of lesser abundance compared to the major plant constituents but, nonetheless, have important plant functions and ecological significance. Additional research is needed to advance our understanding of the spectral influences of plant phenolics and terpenes relative to dominant leaf biochemistry (water, chlorophyll, protein/nitrogen, cellulose, and lignin).

International Journal of Applied Earth Observation

Mineralogy and geochemistry of the No. 6 Coal (Pennsylvanian) in the Junger Coalfield, Ordos Basin, China

This paper discusses the mineralogy and geochemistry of the No. 6 Coal (Pennsylvanian) in the Junger Coalfield, Ordos Basin, China. The results show that the vitrinite reflectance (0.58%) is lowest and the proportions of inertinite and liptinite (37.4% and 7.1%, respectively) in the No. 6 Coal of the Junger Coalfield are highest among all of the Late Paleozoic coals in the Ordos Basin. The No. 6 Coal may be divided vertically into four sections based on their mineral compositions and elemental concentrations. A high boehmite content (mean 6.1%) was identified in the No. 6 Coal. The minerals associated with the boehmite in the coal include goyazite, rutile, zircon, and Pb-bearing minerals (galena, clausthalite, and selenio-galena). The boehmite is derived from weathered and oxidized bauxite in the weathered crust of the underlying Benxi Formation (Pennsylvanian). A high Pb-bearing mineral content of samples ZG6-2 and ZG6-3 is likely of hydrothermal origin. The No. 6 coal is enriched in Ga (44.8 ??g/g), Se (8.2 ??g/g), Sr (423 ??g/g), Zr (234 ??g/g), REEs (193.3 ??g/g), Hg (0.35 ??g/g), Pb (35.7 ??g/ g), and Th (17.8 ??g/g). Gallium and Th in the No. 6 Coal mainly occur in boehmite, and the Pb-bearing selenide and sulfide minerals contribute not only to Se and Pb contents in the coal, but also probably to Hg content. A high Zr content is attributed to the presence of zircon, and Sr is related to goyazite. The REEs in the coal are supplied from the sediment-source region, and the REEs leached from the adjacent partings by groundwater. ?? 2005 Elsevier B.V. All rights reserved.

International Journal of Coal Geology

Mineralogy and geochemistry of a Late Permian coal in the Dafang Coalfield, Guizhou, China: Influence from siliceous and iron-rich calcic hydrothermal fluids

This paper describes the influence of siliceous and iron-rich calcic low-temperature hydrothermal fluids (LTHF) on the mineralogy and geochemistry of the Late Permian No. 11 Coal (anthracitic, Rr =2.85%) in the Dafang Coalfield in northwestern Guizhou Province, China. The No. 11 Coal has high contents of vein ankerite (10.2 vol.%) and vein quartz (11.4 vol.%), with formation temperatures of 85 and 180 ??C, respectively, indicating that vein ankerite and vein quartz were derived from low-temperature calcic and siliceous hydrothermal fluids in two epigenetic episodes. The vein quartz appears to have formed earlier than vein ankerite did, and at least three distinct stages of ankerite formation with different Ca/Sr and Fe/Mn ratios were observed. The two types of mineral veins are sources of different suites of major and trace metals. Scanning electron microscope and sequential extraction studies show that, in addition to Fe, Mg, and Ca, vein ankerite is the dominant source of Mn, Cu, Ni, Pb, and Zn in the coal, and the contents of these five elements are as high as 0.09% and 74.0, 33.6, 185, and 289 ??g/g, respectively. In contrast, vein quartz is the main carrier mineral for platinum-group elements (PGEs) Pd, Pt, and Ir in the coal, and the contents of Pd, Pt, and Ir are 1.57, 0.15, and 0.007 ??g/g, respectively. Sequential extraction showed a high PGE content in the silicate fraction, up to 10.4 ??g/g Pd, 1.23 ??g/g Pt, and 0.05 ??g/g Ir, respectively. It is concluded that the formation of ankerite and quartz and the anomalous enrichment of trace elements in the No. 11 Coal in the Dafang Coalfield, Guizhou, result from the influx of calcic and siliceous low-temperature hydrothermal fluids. ?? 2004 Elsevier B.V. All rights reserved.

International Journal of Coal Geology

Hydrogeology, groundwater flow, and groundwater quality of an abandoned underground coal-mine aquifer, Elkhorn Area, West Virginia

The Pocahontas No. 3 coal seam in southern West Virginia has been extensively mined by underground methods since the 1880’s. An extensive network of abandoned mine entries in the Pocahontas No. 3 has since filled with good-quality water, which is pumped from wells or springs discharging from mine portals (adits), and used as a source of water for public supplies. This report presents results of a three-year investigation of the geology, hydrology, geochemistry, and groundwater flow processes within abandoned underground coal mines used as a source of water for public supply in the Elkhorn area, McDowell County, West Virginia. This study focused on large (> 500 gallon per minute) discharges from the abandoned mines used as public supplies near Elkhorn, West Virginia. Median recharge calculated from base-flow recession of streamflow at Johns Knob Branch and 12 other streamflow gaging stations in McDowell County was 9.1 inches per year. Using drainage area versus mean streamflow relationships from mined and unmined watersheds in McDowell County, the subsurface area along dip of the Pocahontas No. 3 coal-mine aquifer contributing flow to the Turkey Gap mine discharge was determined to be 7.62 square miles (mi2), almost 10 times larger than the 0.81 mi2 surface watershed. Results of this investigation indicate that groundwater flows down dip beneath surface drainage divides from areas up to six miles east in the adjacent Bluestone River watershed. A conceptual model was developed that consisted of a stacked sequence of perched aquifers, controlled by stress-relief and subsidence fractures, overlying a highly permeable abandoned underground coal-mine aquifer, capable of substantial interbasin transfer of water. Groundwater-flow directions are controlled by the dip of the Pocahontas No. 3 coal seam, the geometry of abandoned mine workings, and location of unmined barriers within that seam, rather than surface topography. Seven boreholes were drilled to intersect abandoned mine workings in the Pocahontas No. 3 coal seam and underlying strata in various structural settings of the Turkey Gap and adjacent down-dip mines. Geophysical logging and aquifer testing were conducted on the boreholes to locate the coal- mine aquifers, characterize fracture geometry, and define permeable zones within strata overlying and underlying the Pocahontas No. 3 coal-mine aquifer. Water levels were measured monthly in the wells and showed a relatively static phreatic zone within subsided strata a few feet above the top of or within the Pocahontas No. 3 coal-mine aquifer (PC3MA). A groundwater-flow model was developed to verify and refine the conceptual understanding of groundwater flow and to develop groundwater budgets for the study area. The model consisted of four layers to represent overburden strata, the Pocahontas No. 3 coal-mine aquifer, underlying fractured rock, and fractured rock below regional drainage. Simulation of flow in the flooded abandoned mine entries using highly conductive layers or zones within the model, was unable to realistically simulate interbasin transfer of water. Therefore it was necessary to represent the coal-mine aquifer as an internal boundary condition rather than a contrast in aquifer properties. By representing the coal-mine aquifer with a series of drain nodes and optimizing input parameters with parameter estimation software, model errors were reduced dramatically and discharges for Elkhorn Creek, Johns Knob Branch, and other tributaries were more accurately simulated. Flow in the Elkhorn Creek and Johns Knob Branch watersheds is dependent on interbasin transfer of water, primarily from up dip areas of abandoned mine workings in the Pocahontas No. 3 coal-mine aquifer within the Bluestone River watershed to the east. For the 38th, 70th, and 87th percentile flow duration of streams in the region, mean measured groundwater discharge was estimated to be 1.30, 0.47, and 0.39 cubic feet per square mile (ft3/s/mi2

West Virginia

Using simulated maps to interpret the geochemistry, formation and quality of the Blue Gem Coal Bed, Kentucky, USA

This study presents geostatistical simulations of coal-quality parameters, major oxides and trace metals for an area covering roughly 812 km 2 of the Blue Gem coal bed in southeastern Kentucky, USA. The Blue Gem, characterized by low ash yield and low sulfur content, is an important economic resource. Past studies have characterized the Blue Gem's geochemistry, palynology and petrography and inferred a depositional setting of a planar peat deposit that transitioned to slightly domed later in its development. These studies have focused primarily on vertical geochemical trends within the coal bed. Simulated maps of chemical elements derived from 45 measured sample locations across the study area provide an opportunity to observe changes in the horizontal direction within the coal bed. As the Blue Gem coal bed shows significant vertical chemical trends, care was taken in this study to try to select samples from a single, middle portion of the coal. By revealing spatial distribution patterns of elements across the middle of the bed, associations between different components of the coal can be seen. The maps therefore help to provide a picture of the coal-forming peat bog at an instant in geologic time and allow interpretation of a depositional setting in the horizontal direction. Results from this middle portion of the coal suggest an association of SiO 2 with both K 2 O and TiO 2 in different parts of the study area. Further, a pocket in the southeast of the study area shows elevated concentrations of elements attributable to observed carbonate-phase minerals (MgO, CaO, Ba and Sr) as well as elements commonly associated with sulfide-phase minerals (Cu, Mo and Ni). Areas of relatively high ash yield are observed in the north and south of the mapped area, in contrast to the low ash yields seen towards the east. Additionally, we present joint probability maps where multiple coal-quality parameters are plotted simultaneously on one figure. This application allows researchers to investigate associations of more than two components in a straight-forward manner useful in guiding resource exploration.

Kentucky

Metalliferous coals of the Westphalian A Joggins Formation, Cumberland basin, Nova Scotia, Canada: Petrology, geochemistry, and palynology

Five coals of Westphalian A (early Middle Pennsylvanian) age were sampled from the Joggins Formation section exposed along Chignecto Bay at Joggins, Nova Scotia. Coal beds along the bay were mined beginning in the early 17th century, yet there have been few detailed published investigation of the coal beds of this classic section. The lowermost coal, the Upper Coal 28 (Upper Fundy), is a high-vitrinite coal with a spore assemblage dominated by arboreous lycopsid spores with tree ferns subdominant. The upper portions of the coal bed have the highest ratio of well-preserved to poorly-preserved telinite of any of the coals investigated. Coal 19 ('clam coal') has 88% total vitrinite but, unlike the Fundy coal bed, the telinite has a poor preservation ratio and half the total vitrinite population comprises gelocollinite and vitrodetrinite. The latter coal bed is directly overlain by a basin-wide limestone bed. The Lower Kimberly coal shows good preservation of vitrinite with relatively abundant telinite among the total vitrinite. The Middle Kimberly coal, which underlies the tetrapod-bearing lycopsid trees found by Lyell and Dawson in 1852, exhibits an upward decrease in arboreous lycopod spores and an upward increase in the tree fern spore Punctatisporites minutus. Telinite preservation increases upwards in the Middle Kimberly but overall is well below the preservation ratio of the Upper Fundy coal bed. The coals all have high sulfur contents, yielding up to 13.7% total sulfur for the lower lithotype of the Upper Fundy coal bed. The Kimberly coals are not only high in total and pyritic sulfur, but also have high concentrations of chalcophile elements. Zinc, ranging up to 15,000 ppm (ash basis), is present as sphalerite in fusain lumens. Arsenic and lead each exceed 6000 ppm (ash basis) in separate lithotypes of the Kimberly coals. Together these data are consistent with elevated pH in planar mires. The source of the elemental enrichment in this presumed continental section is enigmatic. (C) 2000 Elsevier Science B.V. All rights reserved.Five coals of Westphalian A (early Middle Pennsylvanian) age were sampled from the Joggins Formation section exposed along Chigneto Bay at Joggins, Nova Scotia. All the coals were found to have high sulfur contents. Overall, the data obtained are consistent with elevated pH in planar mires.

International Journal of Coal Geology

A high-pyrite semianthracite of Late Permian age in the Songzao Coalfield, southwestern China: Mineralogical and geochemical relations with underlying mafic tuffs

The No. 12 Coal (Late Permian) in the Songzao Coalfield, Chongqing, southwestern China, is characteristically high in pyrite and some trace elements. It is uniquely deposited directly above mafic tuff beds. Samples of coal and tuffs have been studied for their mineralogy and geochemistry using inductively coupled plasma-mass spectrometry, X-ray fluorescence, plasma low-temperature ashing plus powder X-ray diffraction, and scanning electron microscopy equipped with energy-dispersive X-ray analysis.The results show that the minerals of the No. 12 Coal are mainly composed of pyrite, clay minerals (kaolinite, chamosite, and illite), ankerite, calcite, and trace amounts of quartz and boehmite. Kaolinite and boehmite were mainly derived from sediment source region of mafic tuffs. Chamosite was formed by the reaction of kaolinite with Fe-Mg-rich fluids during early diagenesis. The high pyrite (Sp,d=8.83%) in the coal was related to marine transgression over peat deposits and abundant Fe derived from the underlying mafic tuff bed. Ankerite and calcite were precipitated from epigenetic fluids.Chemical compositions of incompatible elements indicate that the tuffs were derived from enriched mantle and the source magmas had an alkali-basalt character. Compared to other coals from the Songzao Coalfield and common Chinese coals, the No. 12 Coal has a lower SiO2/Al2O3 (1.13) but a higher Al2O3/Na2O (80.1) value and is significantly enriched in trace elements including Sc (13.5??g/g), V (121??g/g), Cr (33.6??g/g), Co (27.2??g/g), Ni (83.5??g/g), Cu (48.5??g/g), Ga (17.3??g/g), Y (68.3??g/g), Zr (444??g/g), Nb (23.8??g/g), and REE (392??g/g on average). Above mineralogical compositions, as well as similar ratios of selected elements (e.g., SiO2/Al2O3 and Al2O3/Na2O) and similar distribution patterns of incompatible elements (e.g., the mantle-normalized diagram for incompatible elements and chondrite-normalized diagram for rare earth elements) of coal and tuff, indicated that enriched trace elements above were largely derived from mafic tuffs, in addition to a minor amount from the Kandian Oldland. ?? 2010 Elsevier B.V.

International Journal of Coal Geology

Petrography, geochemistry, and depositional setting of the San Pedro and Santo Tomas coal zones: Anomalous algae-rich coals in the middle part of the Claiborne Group (Eocene) of Webb County, Texas

Two coal zones, the San Pedro and the overlying Santo Tomas, are present for nearly 35 km in outcrop, surface and underground mines, and shallow drill holes along the strike of the middle part of the Claiborne Group (Eocene) in Webb County, Texas. A sandstone-dominated interval of 25 to 35 m separates the two coal zones, which range up to 3 m in thickness. Each coal zone contains carbonaceous shales, thin (<0.75 m) impure coal beds, and thin (<0.85 m) but commercially significant nonbanded coal beds. The nonbanded coals are different from other Tertiary coals of the Gulf of Mexico Coastal Plain: unlike lignites that are typical of the older Wilcox Group (Paleocene-Eocene) and younger Jackson Group (Eocene), nonbanded coals of the Claiborne Group have high vitrinite-reflectance values (0.53 R max ) and high calorific yields (average 6670 kcal/kg or 12,000 Btu, dry basis). The coals are weakly agglomerating (free-swelling index is 1.5–2.0) and have an apparent rank of high-volatile bituminous. The coal-bearing portion of the middle Claiborne Group in the Rio Grande area represents a fining-upward transition from sandstone-dominated, marine-influenced, lower delta plain depositional environments to more inland, mudstone-rich, predominantly freshwater deltaic settings. Discontinuities within the San Pedro coal zone are attributed mainly to the influence of contemporaneous deposition of distributary mouth-bar sand bodies. The less variable nature of the Santo Tomas coal zone reflects its origin in the upper part of an interlobe basin that received only minor clastic influx. Petrographic attributes of the nonbanded coals indicate that they formed subaqueously in fresh to possibly brackish waters. A highly degraded groundmass composed of eugelinite is the main petrographic component (approximately 71%, mineral-matter-free basis). An enriched liptinite fraction (approximately 23%) probably accounts for unusually high calorific values. There is negligible inertinite. Petrographic study of polished blocks indicates that approximately 10 percent of the nonbanded coal from both coal zones is composed of green algae fructifications, which also occur in clastic rocks of the coal-bearing interval. Such algal material cannot be identified or quantified by conventional coal petrographic techniques that utilize particle pellets or by palynological analyses that include acid preparation.

International Journal of Coal Geology

Density-stratified flow events in Great Salt Lake, Utah, USA: implications for mercury and salinity cycling

Density stratification in saline and hypersaline water bodies from throughout the world can have large impacts on the internal cycling and loading of salinity, nutrients, and trace elements. High temporal resolution hydroacoustic and physical/chemical data were collected at two sites in Great Salt Lake (GSL), a saline lake in the western USA, to understand how density stratification may influence salinity and mercury (Hg) distributions. The first study site was in a causeway breach where saline water from GSL exchanges with less saline water from a flow restricted bay. Near-surface-specific conductance values measured in water at the breach displayed a good relationship with both flow and wind direction. No diurnal variations in the concentration of dissolved (<0.45 μm) methylmercury (MeHg) were observed during the 24-h sampling period; however, the highest proportion of particulate Hg total and MeHg loadings was observed during periods of elevated salinity. The second study site was located on the bottom of GSL where movement of a high-salinity water layer, referred to as the deep brine layer (DBL), is restricted to a naturally occurring 1.5-km-wide “spillway” structure. During selected time periods in April/May, 2012, wind-induced flow reversals in a railroad causeway breach, separating Gunnison and Gilbert Bays, were coupled with high-velocity flow pulses (up to 55 cm/s) in the DBL at the spillway site. These flow pulses were likely driven by a pressure response of highly saline water from Gunnison Bay flowing into the north basin of Gilbert Bay. Short-term flow reversal events measured at the railroad causeway breach have the ability to move measurable amounts of salt and Hg from Gunnison Bay into the DBL. Future disturbance to the steady state conditions currently imposed by the railroad causeway infrastructure could result in changes to the existing chemical balance between Gunnison and Gilbert Bays. Monitoring instruments were installed at six additional sites in the DBL during October 2012 to assess impacts from any future modifications to the railroad causeway.

Utah