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P.P. Hearn

Publications and source records attributed to P.P. Hearn.

30 records · Page 2Linked to original sources
USGS1993

Do ages of authigenic K-feldspar date the formation of Mississippi valley-type Pb-Zn deposits, central and southeastern United States?: Pb isotopic evidence

Pb concentrations and isotopic compositions have been determined for authigenic over-growths and detrital cores of K-feldspar from Cambrian sedimentary rocks in Texas, Tennessee, and Pennsylvania (referred to as group 1) and southeastern Missouri (referred to as group 2). Overgrowths and cores were separated by abrasion and analyzed separately. In three group 1 samples, cores have Pb isotopic ratios similar to initial ratios in K-feldspar from nearby Middle Proterozoic basement rocks ( 206 Pb/ 204 Pb =16.7-17.0). Pb ratios in overgrowths are radiogenic ( 206 Pb/ 204 Pb up to 19.3) and mostly are distinct from those in ore deposits in the southern Appalachians. Pb isotopic data for two samples of K-feldspar from southeastern Missouri are scattered; in one sample, cores and overgrowths contain radiogenic Pb, suggesting at least two periods of authigenic replacement, in agreement with petrographic evidence. Proterozoic material must still be present because 40 Ar/ 39 Ar stepwise analysis of a total (cores plus overgrowths) sample yields incremental ages ranging from about 500 to 750 Ma. The disparity in Pb isotopic ratios of group 1 overgrowths and Pb in nearby Mississippi Valley-type deposits implies that the regional authigenic K-feldspar event was not synchronous with ore deposition in the southeastern United States. In contrast, Pb isotopic ratios from group 2 authigenic K-feldspar are similar to ratios in ores of southeastern Missouri, suggesting a genetic relation in late Paleozoic time.

Geology↗
USGS1990

Intragranular diffusion: An important mechanism influencing solute transport in clastic aquifers?

Quantification of intragranular porosity in sand-size material from an aquifer on Cape Cod, Massachusetts, by scanning electron microscopy, mercury injection, and epifluorescence techniques shows that there are more reaction sites and that porosity is greater that indicated by standard short-term laboratory tests and measurement techniques. Results from laboratory and field tracer tests show solute nonequilibrium for a reacting ion consistent with a model of diffusion into, and exchange within, grain interiors. These data indicate that a diffusion expression needs to be included in transport codes, particularly for simulation of the transport of radioactive and toxic wastes.

Massachusetts↗
USGS1989

Oxygen-isotope composition of ground water and secondary minerals in Columbia Plateau basalts: Implications for the paleohydrology of the Pasco Basin

Concentrations of 18 O and deuterium in ground waters beneath the Hanford Reservation, Washington State, suggest that the meteoric waters recharging the basalt aquifers have been progressively depleted in these isotopes since at least Pleistocene time. This conclusion is supported by oxygen-isotope analyses of low-temperature secondary minerals filling vugs and fractures in the basalts, which are used to approximate the 18 O content of ground water at the time the mineral assemblage formed. A fossil profile of δ 18 O values projected for ground water in a 1500 m vertical section beneath the reservation suggests that the vertical mixing of shallow and deep ground water indicated by present-day hydrochemical data was also occurring during Neogene time. These data also suggest that a unidirectional depletion of 18 O and deuterium recorded in Pleistocene ground waters may have extended considerably further back in time. This shift is tentatively attributed to the orographic depletion of 18 O associated with the progressive uplift of the Cascade Range since the middle Miocene.

Geology↗
USGS1987

Evidence for Late-Paleozoic brine migration in Cambrian carbonate rocks of the central and southern Appalachians: Implications for Mississippi Valley-type sulfide mineralization

Many Lower Paleozoic limestones and dolostones in the Valley and Ridge province of the central and southern Appalachians contain 10 to 25 weight percent authigenic potassium feldspar. This was considered to be a product of early diagenesis, however, 40 Ar 39 Ar "> 40 Ar 39 Ar analyses of overgrowths on detrital K-feldspar in Cambrian carbonate rocks from Pennsylvania, Maryland, Virginia, and Tennessee yield Late Carboniferous-Early Permian ages (278–322 Ma). Simple mass balance calculations suggest that the feldspar could not have formed isochemically, but required the flux of multiple pore volumes of fluid through the rocks, reflecting regional fluid migration events during the Late-Paleozoic Alleghanian orogeny. Microthermometric measurements of fluid inclusions in overgrowths on detrital K-feldspar and quartz grains from unmineralized rocks throughout the study area indicate homogenization temperatures from 100° to 200°C and freezing point depressions of −14° to −18.5°C (18–21 wt.% NaCl equiv). The apparent similarity of these fluids to fluid inclusions in ore and gangue minerals of nearby Mississippi Valley-type (MVT) deposits suggests that the regional occurrences of authigenic K-feldspar and MVT mineralization may be genetically related. This hypothesis is supported by the discovery of authigenic K-feldspar intergrown with sphalerite in several mines of the Mascot-Jefferson City District, E. Tennessee. Regional potassic alteration in unmineralized carbonate rocks and localized occurrences of MVT mineralization are both explainable by a gravity-driven flow model, in which deep brines migrate towards the basin margin under a hydraulic gradient established during the Alleghanian orogeny. The authigenic K-feldspar may reflect the loss of K during disequilibrium cooling of the ascending brines. MVT deposits are probably localized manifestations of the same migrating fluids, occurring where the necessary physical and chemical traps are present.

Geochimica et Cosmochimica Acta↗
USGS1985

Geochemical controls on dissolved sodium in basalt aquifers of the Columbia Plateau, Washington

Miocene basaltic aquifers of the Columbia Plateau are the principal source of water for agricultural, domestic, and municipal use in Washington State. Irrigation with groundwaters with relatively high sodium concentrations has been cause for concern in recent years, because of the tendency of such waters to reduce soil permeability. Chemical reactions involving groundwater and the basalts are the primary mechanisms responsible for the input of sodium to groundwater in the plateau. This conclusion is supported by the sequence of secondary alteration products found and by progressive changes in groundwater chemistry with depth and position along regional flow paths. Upgradient and shallow groundwaters have low sodium concentrations and sodium-adsorption ratios (SAR's), and are predominantly calcium sodium bicarbonate waters. Groundwaters from deeper and downgradient locations have higher sodium concentrations and SAR 's and are predominantly sodium bicarbonate water. Volcanic glass and cryptocrystalline matrix are the major sources of groundwater sodium, and are dissolved by a combination of silicate hydrolysis and dissolution by carbonic acid. Magnesium, iron, and calcium are removed from solution by the formation of an iron magnesium smectite, calcite , and amorphous iron oxyhydroxide. The addition of sodium, silicon, and potassium by dissolution of basalt exceeds their removal by the precipitation of secondary minerals, and their concentrations increase in the initial stages of this process. In later stages, these continued increases produce a water saturated with clinoptilolite and silica phases, and these begin to precipitate. While the timing of these processes is unclear, the mineralogy of secondary alteration and estimated cooling rates of the basalt flows suggest that observed alteration products formed primarily at low temperature, under conditions similar to those existing at the present time. (USGS)

Water-Resources Investigations Report↗
USGS1984

CHARACTERIZATION OF SECONDARY ALTERATION IN THE COLUMBIA RIVER BASALT BY BACKSCATTERED ELECTRON IMAGING AND ENERGY-DISPERSIVE X-RAY SPECTROSCOPY.

The thick sequences of flood basalts which underlie the Columbia River basin are important aquifiers, providing water for both agricultural and domestic use. Secondary alteration in these rocks occurs primarily as coatings or fillings in fractures and vesicles; alteration is generally believed to have occurred at low temperatures ( less than 100 C) by reaction with meteroic waters. The distribution and compositional variation of secondary minerals are therefore of major interest. This paper focuses on the compositional variation of the major alteration products and on present formulas based on the mean composition of these phases, and suggests possible reactions for the observed sequence of alteration.

Conference Paper↗
USGS1983

Authigenic vivianite in Potomac River sediments: control by ferric oxy-hydroxides

Sand-size particles of vivianite (Fe 3 (PO 4 ) 2 .8H 2 O) have been identified in surficial sediments of the tidal Potomac River near a major sewage treatment plant. Vivianite is concentrated in a surface layer of coarse-sand dredge spoil, which overlies much finer sediment. Although saturation indices indicate that the pore waters of virtually all the sediments in the study area are supersaturated with respect to vivianite, it is found only in association with dredge spoil. Pore-water profiles of Fe, P, and Eh, and the size and morphology of individual grains, indicate that the vivianite is authigenic. The major control on the occurrence of the mineral is the presence or absence of amorphous ferric oxy-hydroxides, which react with pore-water phosphorus to form stable ferric hydroxy-phosphates preferentially to the formation of vivianite.--Modified journal abstract.

Journal of Sedimentary Petrology↗