Geology topics

T. K. Hinkley

Publications and source records attributed to T. K. Hinkley.

9 recordsLinked to original sources

USGS2009

Investigation of thallium fluxes from subaerial volcanism-Implications for the present and past mass balance of thallium in the oceans

A suite of 34 volcanic gas condensates and particulates from Kilauea (Hawaii), Mt. Etna and Vulcano (Italy), Mt. Merapi (Indonesia), White Island and Mt. Nguaruhoe (New Zealand) were analysed for both Tl isotope compositions and Tl/Pb ratios. When considered together with published Tl–Pb abundance data, the measurements provide globally representative best estimates of Tl/Pb = 0.46 ± 0.25 and ε 205 Tl = −1.7 ± 2.0 for the emissions of subaerial volcanism to the atmosphere and oceans (ε 205 Tl is the deviation of the 205 Tl/ 203 Tl isotope ratio from NIST SRM 997 isotope standard in parts per 10,000). Compared to igneous rocks of the crust and mantle, volcanic gases were found to have (i) Tl/Pb ratios that are typically about an order of magnitude higher, and (ii) significantly more variable Tl isotope compositions but a mean ε 205 Tl value that is indistinguishable from estimates for the Earth’s mantle and continental crust. The first observation can be explained by the more volatile nature of Tl compared to Pb during the production of volcanic gases, whilst the second reflects the contrasting and approximately balanced isotope fractionation effects that are generated by partial evaporation of Tl during magma degassing and partial Tl condensation as a result of the cooling and differentiation of volcanic gases.

Geochimica et Cosmochimica Acta↗

USGS2001

Trace metal suites in Antarctic pre-industrial ice are consistent with emissions from quiescent degassing of volcanoes worldwide

Trace metals are more abundant in atmospheric load and deposition material than can be due to rock and soil dusts and ocean salt. In pre-industrial ice from coastal west Antarctica, dust and salt account for only a few percent of the lead, cadmium, and indium that is present in most samples, less than half in any sample. For these trace metals, the deposition rate to the pre-industrial ice is approximately matched by the output rate to the atmosphere by quiescent (non-explosive) degassing of volcanoes worldwide, according to a new estimate. The basis of the match is the masses and proportions of the metals, and the proportions of Pb isotopes, in ice and in volcano emissions. The isotopic compositions of Pb in ice are similar to those of a suite of ocean island volcanoes, mostly in the southern hemisphere. The natural baseline values for pre-industrial atmospheric deposition fluxes of trace metal suites at Taylor Dome, and the worldwide quiescent volcano emissions fluxes to which they are linked, constitute a reasonably well-constrained baseline component for deposition fluxes of metals in modern times. ?? 2001 Elsevier Science B.V. All rights reserved.

Earth and Planetary Science Letters↗

USGS2001

Atmospheric regime of dust and salt through 75,000 years of Taylor Dome ice core: Refinement by measurement of major, minor, and trace metal suites

Measurement of absolute and relative amounts of dust and salt deposited in the polar ice record is central to several fields of study, including nutrient delivery, atmospheric deposition of trace elements, past wind strengths, dust provenance, and other aspects of climate and geochemical history. We present a method intended to give a more accurate picture than has been possible before of the total amounts and relative proportions of the dust and salt deposited by the atmosphere into polar ice. It also permits us to distinguish different compositional types of dust in the ice. The method is based on precise measurement of a suite of several metals whose proportions contrast strongly between dust and salt and vary substantially between dust types. We apply the method to a small suite of ice samples from the Taylor Dome core in coastal West Antarctica. In full glacial times, when total impurities were high and dust dominated over salt, wind strength in the West Antarctic region was apparently high, and extensive sea-ice cover prevented incorporation of salt into the atmospheric load. At the termination of the glacial period, increased salt in the dust-salt mixture indicates that sea ice diminished, but wind strength continued high, and unchanged dust composition indicates unchanged source areas. At about 10,000-11,000 y.B.P., sea-ice cover appears to have briefly returned to glacial conditions, but wind conditions remained in the milder postglacial condition. Soon after, sea ice retreated, and an abrupt change in dust composition indicates changed source materials or terranes. If extended by analysis of more samples from more sites, such information on salt and dust could provide firm constraints on past wind strengths, extent of sea-ice cover, deposition fluxes of salt and dust, and changing continental source areas of dust, for both polar regions of the Earth.

Journal of Geophysical Research D: Atmospheres↗

USGS1999

Metal emissions from Kilauea, and a suggested revision of the estimated worldwide metal output by quiescent degassing of volcanoes

Measurements of a large suite of metals (Pb, Cd, Cu, Zn and several others) and sulfur at Kilauea volcano over an extended period of time has yielded a detailed record of the atmospheric injection of ordinarily-rare metals from this quiescently degassing volcano, representative of an important type. We have combined the Kilauea data with data of recent studies by others (emissions from volcanoes in the Indonesian arc; the large Laki eruption of two centuries ago; Etna: estimates of total volcanic emissions of sulfur) to form the basis for a new working estimate of the rate of worldwide injection of metals to the atmosphere by volcanoes. The new estimate is that volcanoes inject a substantially smaller mass of ordinarily-rare metals into the atmosphere than was stated in a widely cited previous estimate [J.O. Nriagu, A global assessment of natural sources of atmospheric trace metals, Nature 338 (1989) 47-49]. Our estimate, which is an upper limit, is an annual injection mass of about 10,000 tons of the metals considered, versus the earlier estimate of about 23,000 tons. Also, the proportions of the metals are substantially different in our new estimate.

Earth and Planetary Science Letters↗

USGS1994

Composition and sources of atmospheric dusts in snow at 3200 meters in the St. Elias Range, southeastern Alaska, USA

Dusts in snow from the accumulation zone in the St. Elias Range appear from their chemical compositions to have come from terranes of rocks of ferromagnesian composition. These dusts, with respect to their composition and to the moderate degree of variation that occurs through a depositional year, are similar those deposited in Greenland. The high portion of the St. Elias Range is isolated from dominance by any local dust source terranes, because of altitude and the extent of the surrounding glacierized and snow-covered region. In Greenland the altitude is typically lower, but local sources are even less likely to dominate the character of the dusts deposited into the ice record there. The similar compositions and moderate compositional variations of dusts from these two places bear on the question of whether the dusts that are transported over long distances by the atmosphere under modern and glacial-period conditions are uniform and representative of a broad regional or even hemispheric background dust. The dusts in the snow were measured by means of a suite of major, minor, and trace rock-forming metals chosen to give information about rock types, their constituent minerals, degree of degradation (weathering), and energies of atmospheric uptake from source. The variations in amounts of rock dust through the year in the St. Elias Range snowpack have no time-stratigraphic correspondence to the also large variations in concentrations of other species that are not constituents of rock-derived dusts, such the anions chloride, sulfate, and nitrate; the highs and lows of the two types of materials are apparently completely independent. The structure revealed by the moderately fine-scale sampling of the present study (≈ 10 increments/y) serves as a background for the interpretation of analysis of ice core samples, in which annual layers may be too compressed to permit analysis of sub-annual samples.

Alaska↗

USGS1994

Fractionation of families of major, minor, and trace metals across the melt-vapor interface in volcanic exhalations

Chemical families of metals fractionate systematically as they pass from a silicate melt across the interface with the vapor phase and on into a cooled volcanic plume. We measured three groups of metals in a small suite of samples collected on filters from the plumes of Kilauea (Hawaii, USA), Etna (Sicily), and Merapi (Java) volcanoes. These were the major, minor, and trace metals of the alkali and alkaline earth families (K, Rb, Cs, Ca, Sr, Ba), a group of ordinarily rare metals (Cd, Cu, In, Pb, Tl) that are related by their chalcophile affinities, and the radon daughter nuclides 210Po, 210Bi, and 210Pb. The measurements show the range and some details of systematic melt-vapor fractionation within and between these groups of metals. In the plumes of all three volcanoes, the alkali metals are much more abundant than the alkaline earth metals. In the Kilauea plume, the alkali metals are at least six times more abundant than the alkaline earth metals, relative to abundances in the melt; at Etna, the factor is at least 300. Fractionations within each family are, commonly, also distinctive; in the Kilauea plume, in addition to the whole alkaline earth family being depleted, the heaviest metals of the family (Sr, Ba) are progressively more depleted than the light metal Ca. In plumes of fumaroles at Merapi, K/Cs ratios were approximately three orders of magnitude smaller than found in other earth materials. This may represent the largest observed enrichment of the "light ion lithophile" (LIL) metals. Changes in metal ratios were seen through the time of eruption in the plumes of Kilauea and Etna. This may reflect degree of degassing of volatiles, with which metals complex, from the magma bodies. At Kilauea, the changes in fractionation were seen over about three years; fractionation within the alkaline earth family increased, and that between the two families decreased, over that time. All of the ordinarily rare chalcophile metals measured are extremely abundant in volcanic plumes, and Cd and Tl are enriched relative to the others. Indium is much more abundant in the plume of the hotspot volcano Kilauea than in the Etna plume (probably non-hotspot in character). It may be a useful indicator of the tapping of deep mantle zones, or could aid in the interpretation of reports of Pt group metals in exhalations from hot spot volcanoes. Indium in old glacial ice strata could help assess magnitude and variability of exhalations from hotspot volcanoes in past time. Strong melt-vapor fractionation of the alkali and alkaline earth metals may only be observed in plumes during quiescent degassing of volcanoes; when large amounts of ash or spatter (undifferentiated lava) enter the plume, its alkali and alkaline earth metal composition may approach that of the melt. Ratios among the chalcophile metals may not be much changed by addition of ash, because their concentrations in melt are so small, and masses of them in any plume may remain dominated by transfer across the melt-vapor interface. Radon daughter nuclides give information about state of volcanic activity at time of sampling. The precisely known origins, ultratrace detectability, decay systematics, and wide variations in volatility of these species provide information about residence times, degassing and travel histories, and identities of melt bodies in volcanic systems. ?? 1994.

Geochimica et Cosmochimica Acta↗

USGS1991

Tritium concentrations in the active Pu'u O'o crater, Kilauea volcano, Hawaii: implications for cold fusion in the Earth's interior

The assertion that deuterium-deuterium fusion may occur at low temperature suggests a potential new source of geothermal heat. If a cold-fusion-like process occurs within the Earth, then a test for its existence would be a search for anomalous tritium in volcanic emissions. The Pu'u O'o crater is the first point at which large amounts of water are degassed from the magma that feeds the Kilauea system. The magma is probably not contaminated by meteoric-source ground water prior to degassing at Pu'u O'o, although mixing of meteoric and magmatic H2O occurs within the crater. Tritium contents of samples from within the crater are lower than in samples taken simultaneously from the nearby upwind crater rim. These results provide no evidence in support of a cold-fusion-like process in the Earth's interior. ?? 1991.

Physics of the Earth and Planetary Interiors↗

USGS1988

Major- and minor-metal composition of three distinct solid material fractions associated with Juan de Fuca hydrothermal fluids (northeast Pacific), and calculation of dilution fluid samples

Three distinct types of solid material are associated with each sample of the hydrothermal fluid that was collected from the vents of the Southern Juan de Fuca Ridge. The solid materials appear to be representative of deposits on ocean floors near mid-ocean ridges, and interpretation of the chemistry of the hydrothermal solutions requires understanding of them. Sr isotopic evidence indicates that at least two and probably all three of these solid materials were removed from the solution with which they are associated, by precipitation or adsorption. This occurred after the "pure" hydrothermal fluid was diluted and thoroughly mixed with ambient seawater. The three types of solid materials, are, respectively, a coarse Zn- and Fe-rich material with small amounts of Na and Ca; a finer material also rich in Zn and Fe, but with alkali and alkaline-earth metals; and a scum composed of Ba or Zn, with either considerable Fe or Si, and Sr. Mineral identification is uncertain because of uncertain anion composition. Only in the cases of Ba and Zn were metal masses greater in solid materials than in the associated fluids. For all other metals measured, masses in fluids dwarf those in solids. The fluids themselves contain greater concentrations of all metals measured, except Mg, than seawater. We discuss in detail the relative merits of two methods of determining the mixing proportions of "pure" hydrothermal solution and seawater in the fluids, one based on Sr isotopes, and another previously used method based on Mg concentrations. Comparison of solute concentrations in the several samples shows that degree of dilution of "pure" hydrothermal solutions by seawater, and amounts of original solutes that were removed from it as solid materials, are not related. There is no clear evidence that appreciable amounts of solid materials were not conserved (lost) either during or prior to sample collection. ?? 1988.

Chemical Geology↗

USGS1979

Effect on sediment yield and water quality of a nonrehabilitated surface mine in north-central Wyoming

Sediment and chemical quality of water data were collected from two adjacent drainage basins in northern Wyoming to compare hydrologic differences between an undisturbed basin and a surface-mined, virtually unrehabilitated basin. Rate of sediment accumulation in a pond in the basin that was surface mined for coal and left unrehabilitated was over 11 times greater than in a pond in the adjacent unmined basin. The additional sediment came primarily from barren high walls and roughly graded spoils. No sediment was yielded from ungraded spoil rows that drained to closed depressions. Most sediment yielded from the two basins was trapped in the two ponds. The chemical composition of materials from slopes, channels, and pond bottoms of the two basins were similar; however, concentrations of dissolved and suspended matter in waters of the two ponds were different. Low concentrations of dissolved chemical constituents in the pond water below the unmined basin suggest surface runoff as the source. Higher concentrations of dissolved chemical constituents , notably calcium, magnesium, and sulfate, in pond water below the mined area suggest ground-water discharge as the source. Sediment yield was a better indicator of the effects of disturbance on mined areas than chemical quality of water. (Woodard-USGS)

Water-Resources Investigations Report↗