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At least 379 records · Page 21Linked to original sources

USGS1990

Mineralogy and geochemistry of altered rocks associated with Lemitar carbonatites, central New Mexico, U.S.A.

The intrusion of more than 100 Cambrian-Ordovician carbonatite dikes caused minor alteration of Proterozoic granitic and mafic rocks in the Lemitar Mountains, although hematization, carbonatization and fenitization caused extensive alteration locally. Ampibolites within 15-20 m of the carbonatite dike contacts were highly altered by carbonatization. Locally the Lemitar diorite/gabbro adjacent to some carbonatites were altered in a thin, discontinuous zone by sodic-potassic fenitization. The granite at Polvadera Peak was locally altered by potassic fenitization. Most of the altered rocks have been further altered by hematization and carbonatization. The altered rocks show increases in loss on ignition and in one or more the elements Ca, K, Na and Al. Only granitic fenites in the Lemitar Mountains lost silica and some diorite/gabbro fenites gained silica. Petrologic and geochemical studies clearly indicate that the types and degree of alteration differ notably in different rock types. The fenitizing fluids were oxidizing, slightly acidic, high in volatiles (especially CO2) and possibly fairly low in alkali elements. ?? 1990.

LITHOS↗

USGS1991

Shoreline deposits and diagenesis resulting from two Late Pleistocene highstands near +5 and +6 metres, Durban, South Africa

In exposures of Pleistocene rocks on the east coast of South Africa, eight sedimentary facies were distinguished on the basis of petrology, grain size, internal structures and field relationships. These are interpreted as deposits of surf zone, breaker zone, swash zone, backbeach, boulder beach and dune environments. Three phases of deposition and diagenesis are recognized. As a result of the stabilising effect of pre-existing coastal facies, the deposits from successive sea level stands are stacked vertically in a narrow coast-normal strip. Early cementation prevented erosion of the deposits during subsequent transgressions. Deposition of subsequent facies took place on an existing coastal dune (Facies 1). A terrace was cut into this dune at a sea level 4.5 to 5 m above present. At this sea level, clastic shoreline sediments were deposited which make up the main sedimentary sequence exposed (Facies 2–7). The steep swash zone, coarse grain size, and comparison with modern conditions in the study area indicate clastic deposition on a high-energy, wave-dominated, microtidal coastline. Vertical stacking of progressively shallower water facies indicates progradation associated with slightly regressive conditions, prior to stranding of the succession above sea level. During a subsequent transgression to 5.5 or 6 m above present sea level, a second terrace was cut across the existing facies, which by then were partly lithified. A boulder beach (Facies 8) deposited on this terrace is indicative of high wave energy and a rocky coastline, formed by existing cemented coastal facies. Comparison with dated deposits from other parts of the South African coast suggest a Late Pleistocene age for Facies 2–8. Deposition was terminated by subsequent regression and continuing low sea levels during the remainder of the Pleistocene. Cementation of the facies took place almost entirely by carbonate precipitation. The presence of isopachous fibrous cements suggests early cementation of Facies 1, 2, 3 and 4 under marine conditions, initially as aragonite which has since inverted to calcite. Facies 5, 6 and 7 are cemented only by equant calcite spar, evidence of cementation in the meteoric phreatic and vadose zones. Lowering of the water table during regression caused the remaining pore space in Facies 1, 2, 3 and 4 to be filled with equant calcite spar. Decementation in a 130 cm wide zone is attributed to water table shifts associated with the later transgression which deposited Facies 8. The vertical stacking of the two depositional sequences may be attributed to rapid cementation of Facies 2, 3, 4, 5, 6 and 7 under humid, subtropical conditions. This lithified sequence then acted as a focus for deposition of coarse-grained shoreline facies (Facies 8) during the subsequent transgression.

Marine Geology↗

USGS1991

Middle to late Cenozoic magmatism of the southeastern Colorado Plateau and central Rio Grande rift (New Mexico and Arizona, U.S.A.): A model for continental rifting

The region of the present Rio Grande rift and southeastern Colorado Plateau underwent lithospheric extension during middle to late Cenozoic deformation affecting the entire southwestern U.S. Lithospheric mantle was disrupted, and in many regions displaced or replaced by asthenospheric mantle at depths from which basaltic magmas were derived and erupted to the surface. Study of the igneous rocks erupted or intruded during this deformation yields insights into processes of magmatism associated with extension of continental lithosphere. Magmatic rocks associated with an early (late Oligocene-early Miocene) ductile phase of extension are dominantly basaltic andesites and related, calc-alkaline intermediate to silicic derivative rocks. Mafic magmas were probably derived from isotopically “enriched” lithospheric mantle. Igneous rocks associated with a later (middle Miocene-Holocene), more brittle phase of extension include widespread basaltic rocks and localized central volcanoes of intermediate to silicic composition. Isotopic compositions of mafic rocks, which include both tholeiitic and alkalic basalts, correlate strongly with tectonic setting and lithospheric structure. Basalts erupted in areas of greatest crustal extension, such as the central and southern rift and Basin and Range province, were derived from isotopically “depleted” (correlated with “asthenospheric”) mantle. Also, isotopic compositions of Pliocene to Holocene basalts are slightly more depleted than those of Miocene basalts, suggesting that subcrustal lithospheric mantle was thinned during late Miocene extension. Intermediate rocks of the central volcanoes formed by a complex combination of processes, probably dominated by fractional crystallization and by assimilation of upper and lower crust in isolated, small magma chambers. The petrologic, geochemical, and isotopic data are compatible with a model, derived first from geophysical data, whereby lithosphere is thinned beneath the central rift and southeastern Colorado Plateau, with greatest thinning centered beneath the axis of the rift. A lithospheric model involving uniform-sense simple shear does not appear compatible with the data as presently understood.

Arizona, New Mexico↗

USGS1994

40Ar/39Ar thermochronologic constraints on the tectonothermal evolution of the northern East Humboldt Range metamorphic core complex, Nevada

The northern East Humboldt Range (NEHR) of northeastern Nevada exposes a suite of complexly deformed migmatitic, upper amphibolite-facies rocks in the footwall of the Ruby Mountains-East Humboldt Range (RM-EHR) detachment fault. New 40 Ar/ 39 Ar data on hornblende, muscovite, biotite, and potassium feldspar help constrain the kinematic and thermal evolution of this terrain during Tertiary extensional exhumation. Hornblende samples from relatively high structural levels yield discordant age spectra that suggest initial cooling during early Tertiary time (63–49 Ma). When coupled with petrological constraints indicating a strongly decompressional P-T-t path above 550°C, the hornblende data suggest that exhumation of the RM-EHR may have initiated in early Tertiary time, approximately coincident with the initial phases of unroofing in the Wood Hills immediately to the east and with the end of thrusting in the late Mesozoic to early Tertiary Sevier orogenic belt of eastern Nevada and western Utah. This temporal coincidence suggests that gravitational collapse of tectonically thickened crust in the internal zone of the Sevier belt could have driven the initial phases of unroofing. Thermal history during the final stage of exhumation of the NEHR is constrained by discordant hornblende cooling ages of 36-29 Ma from deep structural levels and biotite, muscovite, and potassium feldspar cooling ages of 27-21 Ma from a range of structural levels. Comparison of muscovite, biotite, and potassium feldspar cooling ages with previously published fission-track cooling ages implies very rapid cooling rates at temperatures below the closure temperature for muscovite (270°–350°C), but time gaps of > 7 m.y. between hornblende and mica cooling ages suggest that cooling at higher temperatures was more gradual. In addition, comparison of 40 Ar 39 Ar mica cooling ages with previously published fission-track apatite cooling ages suggests pronounced thermal gradients between the NEHR and adjacent areas during latest Oligocene to earliest Miocene time. Such thermal gradients could be readily explained if the RM-EHR detachment fault dipped > 30° between the 300°C and 100°C isotherms. Finally, 40 Ar 39 Ar biotite cooling ages increase southward through the East Humboldt Range, compatible with northward extrapolation of a previously recognized pattern of WNW-younging biotite cooling ages from the Ruby Mountains. A simple model involving the propagation of footwall uplift in the direction of tectonic transport beneath an initially listric normal fault can explain the principle features of the Oligocène to Miocene thermochronologic data set for the RM-EHR.

Nevada↗

USGS1976

Q-mode factor analysis of compositional data

An extended form of the method of Q-mode factor analysis may be used if the rows of the data matrix sum to a constant. The constant row-sum provides a means for scaling the factor model to conform to the units of the original data in such forms as proportions, percentages, or parts per million. The scale factors for an m-factor model are used to derive composition scores and loadings, which lead to the same reproduced data regardless of the choice of reference axes (end-members). Factor-variance diagrams may be constructed to show the proportion of the variance that will be accounted for in each compositional variable by models containing various numbers of end-members. The method may be used to develop a petrologic mixing model by searching for end-members that are geologically plausible. ?? 1976.

Computers & Geosciences↗

USGS1977

The U.S. geological survey rass-statpac system for management and statistical reduction of geochemical data

RASS is an acronym for Rock Analysis Storage System and STATPAC, for Statistical Package. The RASS and STATPAC computer programs are integrated into the RASS-STATPAC system for the management and statistical reduction of geochemical data. The system, in its present form, has been in use for more than 9 yr by scores of U.S. Geological Survey geologists, geochemists, and other scientists engaged in a broad range of geologic and geochemical investigations. The principal advantage of the system is the flexibility afforded the user both in data searches and retrievals and in the manner of statistical treatment of data. The statistical programs provide for most types of statistical reduction normally used in geochemistry and petrology, but also contain bridges to other program systems for statistical processing and automatic plotting. ?? 1977.

Computers & Geosciences↗

USGS1982

Recommended procedures and techniques for the petrographic description of bituminous coals

Modern coal petrology requires rapid and precise description of great numbers of coal core or bench samples in order to acquire the information required to understand and predict vertical and lateral variation of coal quality for correlation with coal-bed thickness, depositional environment, suitability for technological uses, etc. Procedures for coal description vary in accordance with the objectives of the description. To achieve our aim of acquiring the maximum amount of quantitative information within the shortest period of time, we have adopted a combined megascopic-microscopic procedure. Megascopic analysis is used to identify the distinctive lithologies present, and microscopic analysis is required only to describe representative examples of the mixed lithologies observed. This procedure greatly decreases the number of microscopic analyses needed for adequate description of a sample. For quantitative megascopic description of coal microlithotypes, microlithotype assemblages, and lithotypes, we use (V) for vitrite or vitrain, (E) for liptite, (I) for inertite or fusain, (M) for mineral layers or lenses other than iron sulfide, (S) for iron sulfide, and (X 1 ), (X 2 ), etc. for mixed lithologies. Microscopic description is expressed in terms of V representing the vitrinite maceral group, E the exinite group, I the inertinite group, and M mineral components. volume percentages are expressed as subscripts. Thus (V) 20 (V 80 E 10 I 5 M 5 ) 80 indicates a lithotype or assemblage of microlithotypes consisting of 20 vol. % vitrite and 80% of a mixed lithology having a modal maceral composition V 80 E 10 I 5 M 5 . This bulk composition can alternatively be recalculated and described as V 84 E 8 I 4 M 4 . To generate these quantitative data rapidly and accurately, we utilize an automated image analysis system (AIAS). Plots of VEIM data on easily constructed ternary diagrams provide readily comprehended illustrations of the range of modal composition of the lithologic units making up a given coal bed. The use of bulk-specific-gravity determinations is alo recommended for identification and characterization of the distinctive lithologic units. The availability of an AIAS also enhances the capability to acquire textural information. Ranges of size of maceral and mineral grains can be quickly and precisely determined by use of an AIAS. We assume that shape characteristics of coal particles can also be readily evaluated by automated image analysis, although this evaluation has not yet been attempted in our laboratory. Definitive data on the particulate mineral content of coal constitute another important segment of petrographic description. Characterization of mineral content may be accomplished by optical identification, electron microprobe analysis, X-ray diffraction, and scanning and transmission electron microscopy. Individual mineral grains in place in polished blocks or polished this sections, or separated from the coal matrix by sink-float methods are studied by analytical techniques appropriate to the conditions of sampling.

International Journal of Coal Geology↗

USGS1993

Geologic and geomorphic controls of coal development in some Tertiary Rocky Mountain basins, USA

Previous investigations have not well defined the controls on the development of minable coals in fluvial environments. This study was undertaken to provide a clearer understanding of these controls, particularly in of the lower Tertiary coal-bearing deposits of the Raton and Powder River basins in the Rocky Mountain region of the United States. In this region, large amounts of coals accumulated in swamps formed in the flow-through fluvial systems that infilled these intermontane basins. Extrabasinal and intrabasinal tectonism partly controlled the stratigraphic and facies distributions of minable coal deposits. The regional accumulation of coals was favored by the rapid basin subsidence coupled with minimal uplift of the source area. During these events, coals developed in swamps associated with anastomosed and meandering fluvial systems and alluvial fans. The extensive and high rate of sediment input from these fluvial systems promoted the formation of ombrotrophic, raised swamps, which produced low ash and anomalously thick coals. The petrology and palynology of these coals, and the paleobotany of the associated sediments, suggest that ombrotrophic, raised swamps were common in the Powder River Basin, where the climate during the early Tertiary was paratropical. The paleoecology of these swamps is identical to that of the modern ombrotrophic, raised swamps of the Baram and Mahakam Rivers of Borneo.

International Journal of Coal Geology↗

USGS1994

Palynologic and petrographic intervals in the upper Pennsylvanian McLeansboro Group, Western Kentucky

The McLeansboro Group (formerly the Sturgis Formation) in the Western Kentucky coal field spans the upper Desmoinesian (Westphalian D) and the Missourian and Virgilian series (Stephanian). Extensive drilling has demonstrated the lateral continuity of major and minor beds in the group, making it possible to study vertical and lateral changes in palynology and petrology. Significant features of the McLeansboro Group are the marine zones over most of the coals and paleochannels, which are the only disruptions to the continuity of other lithologies. The Desmoinesian Baker (No. 13) and Wheatcroft (No. 13a) coal beds were included in the study but the primary emphasis is on the Missourian and Virgilian coals. Patoka Formation (lower Missourian) coals are dominated by tree fern spores with lesser amounts of sphenopsids, ferns and cordaites spores. This is in marked contrast to the arborescent lycopod-dominated Desmoinesian coals. Only the No. 15 coal bed exceeds 80% vitrinite: the vitrinite content of the No. 16 coal bed is less than 72%, the lowest of any Western Kentucky humic coal. The Bond Formation (upper Missourian) represents a distinct floristic interval, with a greater diversity of plant groups than in the Patoka Formation. Herbaceous lycopod spores, which are relatively minor contributors to the Patoka coals, are common in the Bond Formation. The coals generally exceed 80% vitrinite. The Mattoon Formation (Virgillian) coals have a variety of palynomorph assemblages. The low-sulfur Geiger Lake coal bed is dominated by tree fern spores, with important contributions from other ferns and sphenopsids. Similar to the underlying tree fern interval, vitrinite contents are less than 80%. The uppermost Mattoon coals are dominated by tree ferns and are notable in being the only coals more than 1 m thick in the Stephanian portion of the section, with the top coal being 4.3 m thick. The uppermost coals generally contain more than 80% vitrinite. The Permian Mauzy Formation overlies the McLeansboro Group. The palynologic/petrographic intervals appear to represent fluctuating dry (low vitrinite) and wet intervals within the Stephanian, which was itself drier than the Westphalian D.

International Journal of Coal Geology↗

USGS1975

The Pikes Peak batholith, Colorado front range, and a model for the origin of the gabbro-anorthosite-syenite-potassic granite suite

This study of the Pikes Peak batholith includes the mineralogy and petrology of quartz syenite at West Creek and of fayalite-bearing and fayalite-free biotite granite near Mount Rosa; major element chemistry of the batholith; comparisons with similar postorogenic, intracratonic, sodic to potassic intrusives; and genesis of the batholith. The batholith is elongate in plan, 50 by 100 km, composite, and generally subalkalic. It was emplaced at shallow depth 1,040 m. y. ago, sharply transects its walls and may have breached its roof. Biotite granite and biotite—hornblende granite are predominant; quartz syenite, fayalite granite and riebeckite granite are present in minor amounts. Fayalite-bearing and fayalite-free quartz syenite, fayalite-biotite granite and riebeckite granite show a well-defined sodic differentiation trend; the less sodic fayalite-free granites exhibit a broader compositional range and no sharp trends. Crystallization was largely at P H2O < P total ; P H2O approached P total only at late stages. Aplite residual to fayalite-free biotite granite in the north formed at about 1,500 bars, or 5 km depth. Feldspar assemblages indicate late stages of crystallization at about 720°C. In the south ilmenite and manganian fayalite indicate f O2 of 10 −17 or 10 −18 bars. Biotite and fayalite compositions and the ‘granite minimum’ imply completion of crystallization at about 700°C and 1,500 bars. Nearby fayalite-free biotite granite crystallized at higher water fugacity. All types of syenite and granite contain 5–6% K 2 O through a range of SiO 2 of 63–76%. Average Na 2 O percentages in quartz syenite are 6.2, fayalite granite 4.2, and fayalite-free granite 3.3 MgO contents are low, 0.03–0.4%; FeO averages 1.9–2.5%. FeO/Fe 2 O 3 ratios are high. Fluorine ranges from 0.3 to 0.6%. The Pikes Peak intrusives are similar in mode of emplacement, composition, and probably genesis to rapakivi intrusives of Finland, the Younger Granites of Nigeria, Cape Ann Granite and Beverly Syenite, Mass., and syenite of Kungnat, Greenland, among others — allowing for different levels of erosion. A suite that includes gabbro or basalt, anorthosite, quartz syenite, fayalite granite, riebeckite granite, and biotite and/or hornblende granites is of worldwide occurrence. A model is proposed in which mantle-derived, convecting alkali olivine basaltic magma first reacts with K 2 O-poor lower crust of granulite facies to produce magma of quartz syenitic composition. The syenitic liquid in turn reacts with granodioritic to granitic intermediate crust of amphibolite facies to produce the predominant fayalite-free biotite and biotite-hornblende granites of the batholith. This reaction of magma and roof involves both partial melting and the reconstitution and precipitation of refractory phases, as Bowen proposed. Intermediate liquids include MgO-depleted and Na 2 O-enriched gabbro, which precipitated anorthosite, and alkali diorite. The heat source is the basaltic magma; the heat required for partial melting of the roof is supplied largely by heats of crystallization of phases that settle out of the liquid — mostly olivine, clinopyroxene and plagioclase.

Colorado↗

USGS1985

Characterization of the Sukinda and Nausahi ultramafic complexes, Orissa, India by platinum-group element geochemistry

Samples of 20 chromitite, 14 ultramafic and mafic rock, and 9 laterite and soil samples from the Precambrian Sukinda and Nausahi ultramafic complexes, Orissa, India were analyzed for platinum-group elements (PGE). The maximum concentrations are: palladium, 13 parts per billion (ppb); platinum, 120 ppb; rhodium, 21 ppb; iridium, 210 ppb; and ruthenium, 630 ppb. Comparison of chondrite-normalized ratios of PGE for the chromitite samples of lower Proterozoic to Archean age with similar data from Paleozoic and Mesozoic ophiolite complexes strongly implies that these complexes represent Precambrian analogs of ophiolite complexes. This finding is consistent with the geology and petrology of the Indian complexes and suggests that plate-tectonic and ocean basin development models probably apply to some parts of Precambrian shield areas.

Precambrian Research↗

USGS1994

The 1989-1990 eruptions of Redoubt Volcano: an introduction

Redoubt Volcano, located on the west side of Cook Inlet in south-central Alaska, erupted explosively on over 20 separate occasions between December 14, 1989 and April 21, 1990. Fourteen lava domes were emplaced in the summit area, thirteen of which were subsequently destroyed. The eruption caused economic losses estimated at over $160,000,000 making this the second most costly eruption in U.S. history. This economic impact provided the impetus for a integrated comprehensive account of an erupting volcano using both modern and classical research and modern techniques which in turn led to advances in eruption monitoring and interpretation. Research on such topics as dome formation and collapse and the resulting pyroclastic flows, elutriated ash, lightning, tephra, and flooding was blended with the rapid communication of associated hazards to a large user group. The seismology successes in predicting and monitoring eruption dynamics were due in part to (1) the recognition of long-period seismic events as indicators of the readiness of the volcano to erupt, and (2) to the development of new tools that allowed the seismicity to be assessed instantaneously. Integrated studies of the petrology of erupted products and volatile content over time gave clues as to the progress of the eruption towards completion.

Alaska↗

USGS2020

The contributions and influence of two Americans, Henry S. Washington and Frank A. Perret, to the study of Italian volcanism with emphasis on volcanoes in the Naples area

A century ago, two Americans, Henry Stephens Washington and Frank Alvord Perret, made significant contributions to the geology, petrology, and volcanology of Italy, in particular to those volcanoes in the Naples area, Vesuvius, Campi Flegrei (Phlegraean Fields), and the Island of Ischia. Both were from the eastern United States, both were born in 1867, and both studied physics as undergraduates. However, each man followed a different scientific path and approach in his volcanological studies. Washington was classically trained and more interested in rock chemistry, mineralogy, and petrogenesis. Perret was a gifted inventor, worked in Edison's laboratory, established his own company, and was a keen observer of volcanic phenomena and processes; today he would be called a “physical volcanologist” Each man published classic works on Italian volcanoes, The Roman Comagmatic Region (Washington, 1906) and The Vesuvius Eruption of 1906 (Perret, 1924); both were published by the Carnegie Institution of Washington. However, both men had cosmopolitan tastes for other volcanoes, and they traveled widely and made significant contributions to the knowledge of other volcanic areas. The following two sections present, albeit briefly, their work, significance, and influence to Italian volcanism with emphasis on those volcanoes in the Naples area.

Naples↗

USGS2005

Statistical characterization of a large geochemical database and effect of sample size

The authors investigated statistical distributions for concentrations of chemical elements from the National Geochemical Survey (NGS) database of the U.S. Geological Survey. At the time of this study, the NGS data set encompasses 48,544 stream sediment and soil samples from the conterminous United States analyzed by ICP-AES following a 4-acid near-total digestion. This report includes 27 elements: Al, Ca, Fe, K, Mg, Na, P, Ti, Ba, Ce, Co, Cr, Cu, Ga, La, Li, Mn, Nb, Nd, Ni, Pb, Sc, Sr, Th, V, Y and Zn. The goal and challenge for the statistical overview was to delineate chemical distributions in a complex, heterogeneous data set spanning a large geographic range (the conterminous United States), and many different geological provinces and rock types. After declustering to create a uniform spatial sample distribution with 16,511 samples, histograms and quantile-quantile (Q-Q) plots were employed to delineate subpopulations that have coherent chemical and mineral affinities. Probability groupings are discerned by changes in slope (kinks) on the plots. Major rock-forming elements, e.g., Al, Ca, K and Na, tend to display linear segments on normal Q-Q plots. These segments can commonly be linked to petrologic or mineralogical associations. For example, linear segments on K and Na plots reflect dilution of clay minerals by quartz sand (low in K and Na). Minor and trace element relationships are best displayed on lognormal Q-Q plots. These sensitively reflect discrete relationships in subpopulations within the wide range of the data. For example, small but distinctly log-linear subpopulations for Pb, Cu, Zn and Ag are interpreted to represent ore-grade enrichment of naturally occurring minerals such as sulfides. None of the 27 chemical elements could pass the test for either normal or lognormal distribution on the declustered data set. Part of the reasons relate to the presence of mixtures of subpopulations and outliers. Random samples of the data set with successively smaller numbers of data points showed that few elements passed standard statistical tests for normality or log-normality until sample size decreased to a few hundred data points. Large sample size enhances the power of statistical tests, and leads to rejection of most statistical hypotheses for real data sets. For large sample sizes (e.g., n > 1000), graphical methods such as histogram, stem-and-leaf, and probability plots are recommended for rough judgement of probability distribution if needed. ?? 2005 Elsevier Ltd. All rights reserved.

Applied Geochemistry↗

USGS2011

Hydrogeochemical processes governing the origin, transport and fate of major and trace elements from mine wastes and mineralized rock to surface waters

The formation of acid mine drainage from metals extraction or natural acid rock drainage and its mixing with surface waters is a complex process that depends on petrology and mineralogy, structural geology, geomorphology, surface-water hydrology, hydrogeology, climatology, microbiology, chemistry, and mining and mineral processing history. The concentrations of metals, metalloids, acidity, alkalinity, Cl - , F - and SO 4 2- found in receiving streams, rivers, and lakes are affected by all of these factors and their interactions. Remediation of mine sites is an engineering concern but to design a remediation plan without understanding the hydrogeochemical processes of contaminant mobilization can lead to ineffective and excessively costly remediation. Furthermore, remediation needs a goal commensurate with natural background conditions rather than water-quality standards that might bear little relation to conditions of a highly mineralized terrain. This paper reviews hydrogeochemical generalizations, primarily from US Geological Survey research, that enhance our understanding of the origin, transport, and fate of contaminants released from mined and mineralized areas. Mobility of potential or actual contaminants from mining and mineral processing activities depends on (1) occurrence : is the mineral source of the contaminant actually present? (2) abundance : is the mineral present in sufficient quantity to make a difference? (3) reactivity : what are the energetics, rates, and mechanisms of sorption and mineral dissolution and precipitation relative to the flow rate of the water? and (4) hydrology : what are the main flow paths for contaminated water? Estimates of relative proportions of minerals dissolved and precipitated can be made with mass-balance calculations if minerals and water compositions along a flow path are known. Combined with discharge, these mass-balance estimates quantify the actual weathering rate of pyrite mineralization in the environment and compare reasonably well with laboratory rates of pyrite oxidation except when large quantities of soluble salts and evaporated mine waters have accumulated underground. Quantitative mineralogy with trace-element compositions can substantially improve the identification of source minerals for specific trace elements through mass balances. Post-dissolution sorption and precipitation (attenuation) reactions depend on the chemical behavior of each element, solution composition and pH, aqueous speciation, temperature, and contact-time with mineral surfaces. For example, little metal attenuation occurs in waters of low pH (<3.5) and metals tend to maintain element ratios indicative of the main mineral or group of minerals from which they dissolved, except Fe, SiO 2 , and redox-sensitive oxyanions (As, Sb, Se, Mo, Cr, V). Once dissolved, metal and metalloid concentrations are strongly affected by redox conditions and pH. Iron is the most reactive because it is rapidly oxidized by bacteria and archaea and Fe(III) hydrolyzes and precipitates at low pH (1–3) which is related directly to its first hydrolysis constant, pK 1 = 2.2. Several insoluble sulfate minerals precipitate at low pH including anglesite, barite, jarosite, alunite and basaluminite. Aluminum hydrolyzes near pH 5 (pK 1 = 5.0) and provides buffering and removal of Al by mineral precipitation from pH 4–5.5. Dissolved sulfate behaves conservatively because the amount removed from solution by precipitation is usually too small relative to the high concentrations in the water column and relative to the flow rate of the water.

Applied Geochemistry↗

USGS2026

Prolonged cooling of andesitic-dacitic lava flows produces optimal groundmass material for 40Ar/39Ar dating

Organizing the eruptive histories and petrogenetic models that underpin hazard assessments at active volcanoes typically requires high-precision ages for late Pleistocene to Holocene lava flows. In this study, features of an existing 40Ar/39Ar dataset for andesitic-dacitic rocks from Ruapehu volcano, Aotearoa New Zealand, were interrogated with new microanalytical data to identify the optimal groundmass material for age determination. To understand the behavior of K and Ar within the cooling melt of lavas during their emplacement, we examined and compared the petrological features of samples from the ice-chilled margin and interior of a lava flow. The groundmass of the rapidly cooled sample comprises non-vesicular rhyolitic glass and microlites of plagioclase, orthopyroxene, and magnetite. The sample from the flow interior has minimal amounts of groundmass glass, and interstices are instead occupied by sanidine and tridymite. Modelling supports the interpretation that sanidine crystallized as a stable groundmass phase during slow cooling of degassed melt in the interior zones of lavas that were insulated behind their glassy margins. Our evaluation of the age data shows that sanidine contributed high yields of radiogenic argon during step-heating experiments for samples collected from lava interiors, which enabled high-precision 40Ar/39Ar ages to be determined. Using Ruapehu as an example of an arc volcano affected by lava-ice interaction, we provide a basic field guide for identifying lava flows that contain groundmass sanidine at the expense of glass. Target outcrops also offer opportunities for reconstructing geomagnetic dynamics and volcano–climate relationships during the Pleistocene and Holocene.

Ruapehu volcano↗

USGS2006

Chemical evolution of Miocene wood: Example from the Belchatow brown coal deposit, central Poland

Miocene conifer wood samples from the Belchatow brown coal deposit in Poland were studied in order to discuss a range of chemical variations that occur as a result of biochemical coalification. Petrographic analysis, ultimate analysis, electron microprobe technique, and FTIR spectroscopy were used in this study. Our data show several progressive trends in functional groups distribution that take place during the wood transformation from group 1 to group 4, such as an overall increase in aromaticity, an increase in lignin/cellulose ratio, and an increase in oxygen functionalities. Other observations include an increase in aliphatic stretching and bending functionalities from groups 1 to 3; followed by a decrease in the wood of group 4; appearance of aliphatic out-of-plane bands in group 3 and increase in group 4; an increase in CH2/CH3 in group 4 compared to the other groups; and decrease in O-H groups in group 4 compared to other groups. These observations, together with other chemical and petrological observations, indicate that the progressive elimination of cellulose and modification of lignin are dominant processes of the wood transformation. ?? 2005 Elsevier B.V. All rights reserved.

International Journal of Coal Geology↗

USGS2006

Influence of particle and surface quality on the vitrinite reflectance of dispersed organic matter: Comparative exercise using data from the qualifying system for reflectance analysis working group of ICCP

The development of a qualifying system for reflectance analysis has been the scope of a working group within the International Committee for Coal and Organic Petrology (ICCP) since 1999, when J. Koch presented a system to qualify vitrinite particles according to their size, proximity to bright components and homogeneity of the surface. After some years of work aimed at improving the classification system using photomicrographs, it was decided to run a round robin exercise on microscopy samples. The classification system tested consists of three qualifiers ranging from excellent to low quality vitrinites with an additional option for unsuitable vitrinites. This paper reports on the results obtained by 22 analysts who were asked to measure random reflectance readings on vitrinite particles assigning to each reading a qualifier. Four samples containing different organic matter types and a variety of vitrinite occurrences have been analysed. Results indicated that the reflectance of particles classified as excellent, good or poor compared to the total average reflectance did not show trends to be systematically lower or higher for the four samples analysed. The differences in reflectance between the qualifiers for any given sample were lower than the scatter of vitrinite reflectance among participants. Overall, satisfactory results were obtained in determining the reflectance of vitrinite in the four samples analysed. This was so for samples having abundant and easy to identify vitrinites (higher plant-derived organic matter) as well as for samples with scarce and difficult to identify particles (samples with dominant marine-derived organic matter). The highest discrepancies were found for the organic-rich oil shales where the selection of the vitrinite population to measure proved to be particularly difficult. Special instructions should be provided for the analysis of this sort of samples. The certainty of identification of the vitrinite associated with the vitrinite reflectance values reported has been assessed through a reliability index which takes into account the number of readings and the coefficient of variation. The same statistical approach as that followed in the ICCP vitrinite reflectance accreditation program for single seam coals has been used for data evaluation. The results indicated low to medium dispersion for 17 out of 22 participants. This, combined with data from other sets of comparative analyses over a long period, is considered an encouraging result for the establishment of an accreditation program on vitrinite reflectance measurements in dispersed organic matter. ?? 2006 ICCP.

International Journal of Coal Geology↗