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At least 19 recordsLinked to original sources

Thermodynamic evaluation and restoration of volcanic gas analyses: An example based on modern collection and analytical methods

Thermodynamic evaluation and restoration procedures are applied to a set of 10 volcanic gas analyses obtained by modern collection and analytical methods. The samples were collected from a vigorously fuming fissure during episode 1 of the Puu Oo eruption of Kilauea Volcano in 1983. A variety of analytical techniques were used to determine the gas compositions. In most samples, the combined amounts of N2 + Ar + O2 are far less abundant than H2, CO, or H2S, suggesting little or no contamination or reaction with atmospheric gases. Thermodynamic evaluation shows that 6 of the 10 analyses are equilibrium compositions, and 4 analyses are disequilibrium compositions. Three of the disequilibrium analyses involve samples affected by minor spilling of NaOH solution from the sample bottles during collection. The deviation of these analyses from equilibrium is dominated by the effects of disequilibrium water-loss. The fourth disequilibrium analysis is contaminated with meteoric water. In all 4 cases, the restoration procedures retrieve the original equilibrium compositions. -from Author

Geochemical Journal↗

Scanning electron microscope observations of sublimates from Merapi Volcano, Indonesia

Sublimates were sampled from high-temperature (up to 800°C) fumaroles at Merapi volcano, Indonesia in January 1984. Sampling is accomplished by inserting silica tubes into high-temperature vents. Volcanic gas flows through the tubes and sublimates precipitate on the inner walls in response to the temperature gradient. With decreasing temperature (800–500°C) in the tubes, there are five sublimate zones: 1) cristobalite, magnetite, and halite; 2) halite, sylvite, K-Ca sulfate (K 2 Ca[SO 4 ] 2 ), acmite, wollastonite, and pyrite; 3) halite, sylvite, galena, Pb-Bi sulfide, aphthitalite, sphalerite, and Cs-K sulfate; 4) halite, sylvite, galena, PbKCl 3 , aphthitalite, and Na-K-Fe sulfate ([Na, K] 2 Fe[SO 4 ]Cl 2 ); and 5) halite, sylvite, galena, PbKCl 3 , and various sulfates of Pb, Cu, and Zn. Texturally, the sublimate phases grade from large, well-formed crystals at their highest-temperature occurrence to more numerous, smaller crystals that are less perfect at lower temperatures. These changes imply that the crystal nucleation and growth rates increase and decrease, respectively, as temperature decreases. Several of the sublimate phases also exhibit highly anisotropic morphologies (whiskers, platelets, spheres), especially below their highest temperature of deposition. Overall, the textural data suggest that the gas is saturated or slightly supersaturated with the phases at their hottest occurrence, but that the gas becomes increasingly supersaturated with the phases at lower temperatures. The anisotropic morphologies probably form because the crystals grow toward more supersaturated conditions in the center of the tube. The gas fails to maintain equilibrium with the precipitating sublimates because the high velocity of the carrier gas prevents complete mass transfer from the gas stream to the tube walls.

Merapi Volcano↗

Six years of change in Lake Nyos, Cameroon, yield clues to the past and cautions for the future

The catastrophic release of gas from Lake Nyos, Cameroon, in 1986 caused substantial but incomplete mixing of the stratified water column. The post-release evolution of water-column structure has been monitored through April 1992. Changes began immediately after the event as rainfall and inflow brought dilute fluid into the surface layer. Inflow and surface mixing have gradually deepened the chemocline. The Total Dissolved Solids (TDS) values in the upper 40 m of the water column have dropped from a few hundred mg/kg just after the release to <100 mg/kg. The chemocline is presently strongest at 50 m depth; 5 m below this, the TDS = 570 mg/kg. From 55 to 150 m depth is a gentle gradient in which TDS reaches 920 mg/kg. Little change in water-column chemistry has occurred in this depth interval since the release. Between 150 m depth and lake bottom at 210 m depth, a strong secondary chemocline has formed. Temperature, CO 2 concentration ([CO 2 ]), and TDS have all increased in the deepest layer in response to recharge by warm, mineralized water, reaching values of 25.0°C, 320 mmol/kg, and 1800 mg/kg, respectively, 1 m above lake bottom. Considering all these changes in part as a “recovery” process, it is possible to construct a model of the pre-release water column. The data indicate that the pre-release chemocline was at least 50 m deep. Above the chemocline was a dilute layer containing a seasonal thermocline; below the chemocline was probably a gradient zone(s) with correlated increases in TDS and [CO 2 ] and a secondary chemocline near lake bottom. Maximum values of TDS and [CO 2 ] calculated for pre-release bottom water are 2400 mg/kg and 430 mmol/kg, respectively, based on tritium data. From this pre-release structure, a model of the gas release is proposed that is consistent with available chemical and observational data. An important feature of the model is that disruption of the pre-existing stratification was much more extensive than previously proposed, and even the deepest water layers were involved in the event. This model is not intended to limit possible gas release mechanisms, and thus complete re-establishment of pre-1986 water-column conditions is not a prerequisite for a future release. Spontaneous instability could occur at lake bottom in <20 yr if dissolved gas pressures continue to increase in this zone by 0.5–1 bar/yr as they have for the last 6 yr.

Lake Nyos↗

Lead and strontium isotopes in volcanic rocks from northern Honshu, Japan

Isotopic compositions of lead and strontium and concentrations of lead, uranium, thorium, rubidium, and strontium were measured in a suite of volcanic rocks, ranging from basalt to rhyodacite in composition, and in granite and gabbro xenoliths from a traverse across northern Honshu. The observed 238 U/ 204 Pb (μ) ratio ranges from 2.4 in tholeiitic basalt at the east end of the traverse to 11.6 in alkalic basalt from the west end. The isotopic composition is slightly less radiogenic to the west. The 87 Sr/ 86 Sr ratios of most of the samples fall within the range observed in oceanic basalts, but the granite xenolith and the rhyodacite are slightly more radiogenic.

Honshu↗

Isotopic composition of lead in volcanic rocks from central Honshu — with regard to basalt genesis

The isotopic composition of lead and concentrations of lead, uranium, and thorium were determined in tholeiitic and high-alumina basalts, and their calc-alkali rock series, from central Japan. The isotopic composition of lead of high alumina basalts is similar to that of tholeiites from adjacent areas, whereas their silicic differentiates (calc-alkali rock series) are rich in 207 Pb and 208 Pb. This is interpreted as a result of crustal contamination. The isotopic composition of lead in the primary basalts gradually decreases in radiogenic character from the Pacific Ocean side to the Japan Sea side, whereas the observed 238 U/ 204 Pb and 232 Th/ 238 U ratios in the basalts increase in the same direction. This inverse correlation can be interpreted as resulting from differentiation of the upper mantle about 3.6b.y. ago, with tholeiite (Pacific side) generated from a shallower zone than the alkali basalt (Japan Sea side). The magma generation is associated with a process which extracts Pb preferentially to U and Th at shallower depth and U and Th preferentially to Pb at deeper depth in the past (multi differentiation for the source region) or at the magma generation stage. An alternative interpretation of this inverse correlation is that the ocean floor is being thrust under the Japanese Island arcs and the isotopic difference is produced by the degree of mixing of mantle material under the arcs with thrust material.

Honshu↗

Determination of lead, cadmium, indium, thallium and silver in ancient ices from Antarctica by isotope dilution-thermal ionization mass spectrometry

The concentrations of five chalcophile elements (Pb, Cd, In, Tl and Ag) and the lead isotope ratios in ancient ices from the Taylor Dome near coastal Antarctica, have been determined by the isotope dilution-thermal ionization mass spectrometry (ID-TIMS), with ultra-clean laboratory techniques. The samples were selected from segments of cores, one of which included a visible ash layer. Electric conductivity measurement (ECM) or dielectric properties (DEP) gave distinctive sharp peaks for some of the samples chosen. Exterior portions of the sample segments were trimmed away by methods described here. Samples were evaporated to dryness and later separated into fractions for the five elements using an HBr-HNO 3 anion exchange column method. The concentrations are in the range 2.62-36.7 pg Pb/g of ice, 0.413-2.83 pg Cd/g, 0.081-0.34 pg ln/g, 0.096-2.8 pg Tl/g and 0.15-0.84 pg Ag/g, respectively. The dispersions in duplicate analyses are about ±1% for lead and cadmium, ±2% for indium, ±4% for thallium and ±6% for silver, respectively. The concentrations of lead obtained are commonly higher than those in the present-day Antarctic surface snows, but the isotope ratios are distinctively higher than those of the present-day snows and close to those of the other ancient ice collected from a different Antarctic area.

Geochemical Journal↗

Evaluation on determination of iodine in coal by energy dispersive X-ray fluorescence

A quick and inexpensive method of relative high iodine determination from coal samples was evaluated. Energy dispersive X-ray fluorescence (EDXRF) provided a detection limit of about 14 ppm (3 times of standard deviations of the blank sample), without any complex sample preparation. An analytical relative standard deviation of 16% was readily attainable for coal samples. Under optimum conditions, coal samples with iodine concentrations higher than 5 ppm can be determined using this EDXRF method. For the time being, due to the general iodine concentrations of coal samples lower than 5 ppm, except for some high iodine content coal, this method can not effectively been used for iodine determination. More work needed to meet the requirement of determination of iodine from coal samples for this method. Copyright ?? 2005 by The Geochemical Society of Japan.

Geochemical Journal↗

A stream sediment geochemical survey of the Ganga River headwaters in the Garhwal Himalaya

This study models geochemical and adjunct geologic data to define provinces that are favorable for radioactive-mineral exploration. A multi-element bed-sediment geochemical survey of streams was carried out in the headwaters region of the Ganga River in northern India. Overall median values for uranium and thorium (3.6 and 13.8 ppm; maxima of 4.8 and 19.0 ppm and minima of 3.1 and 12.3 ppm respectively) exceed average upper crustal abundances (2.8 and 10.7 ppm) for these radioactive elements. Anomalously high values reach up to 8.3 and 30.1 ppm in thrust zone rocks, and 11.4 and 22.5 ppm in porphyroids. At their maxima, these abundances are nearly four- and three-fold (respectively) enriched in comparison to average crustal abundances for these rock types. Deformed, metamorphosed and sheared rocks are characteristic of the main central thrust zone (MCTZ). These intensively mylonitized rocks override and juxtapose porphyritic (PH) and proterozoic metasedimentary rock sequences (PMS) to the south. Granitoid rocks, the major protoliths for mylonites, as well as metamorphosed rocks in the MCT zone are naturally enriched in radioelements; high values associated with sheared and mylonitized zones are coincident with reports of radioelement mineralization and with anomalous radon concentrations in soils. The radioelement abundance as well as REE abundance shows a northward enrichment trend consistent with increasing grade of metamorphism indicating deformation-induced remobilization of these elements. U and Th illustrate good correlation with REEs but not with Zr. This implies that zircon is not a principal carrier of U and Th within the granitoid-dominant thrust zone and that other radioelement-rich secondary minerals are present in considerable amounts. Thus, the relatively flat, less fractionated, HREE trend is also not entirely controlled by zircon. The spatial correlation of geologic boundary zones (faults, sheared zones) with geochemical and with geophysical (Rn) anomalies infers ore mineralization by hydrothermal processes generated during multiple episodes of deformation and thrusting. The geologic setting of the anomalies also suggests that crystalline rocks (MCT Zone) along the nearly 2500 km length of the LesserHimalayan belt, where in the vicinity of thrust and fault zones, have potential for radioelement mineralization. Zones of higher concentrations of radioelements delineated by this study and locations of anomalous radon discharge determined by other investigations may indicate a potential health hazard over the long term. However, the low human population density precludes direct manifestation of health effects attributable to chronic exposure to these radioelements; however, the magnitude of natural concentrations suggests the need for more detailed studies and monitoring.

Geochemical Journal↗

Evolution of CO2 in Lakes Monoun and Nyos, Cameroon, before and during controlled degassing

Evolution of CO 2 in Lakes Monoun and Nyos (Cameroon) before and during controlled degassing is described using results of regular monitoring obtained during the last 21 years. The CO 2(aq) profiles soon after the limnic eruptions were estimated for Lakes Monoun and Nyos using the CTD data obtained in October and November 1986, respectively. Based on the CO 2(aq) profiles through time, the CO 2 content and its change over time were calculated for both lakes. The CO 2 accumulation rate calculated from the pre-degassing data, was constant after the limnic eruption at Lake Nyos (1986-2001), whereas the rate appeared initially high (1986-1996) but later slowed down (1996-2003) at Lake Monoun. The CO 2 concentration at 58 m depth in Lake Monoun in January 2003 was very close to saturation due to the CO 2 accumulation. This situation is suggestive of a mechanism for the limnic eruption , because it may take place spontaneously without receiving an external trigger. The CO 2 content of the lakes decreased significantly after controlled degassing started in March 2001 at Lake Nyos and in February 2003 at Lake Monoun. The current content is lower than the content estimated soon after the limnic eruption at both lakes. At Monoun the degassing rate increased greatly after February 2006 due to an increase of the number of degassing pipes and deepening of the pipe intake depth. The current CO 2 content is ∼40% of the maximum content attained just before the degassing started. At current degassing rates the lower chemocline will subside to the degassing pipe intake depth of 93 m in about one year. After this depth is reached, the gas removal rate will progressively decline because water of lower CO 2(aq) concentration will be tapped by the pipes. To keep the CO 2 content of Lake Monoun as small as possible, it is recommended to set up a new, simple device that sends deep water to the surface since natural recharge of CO 2 will continue. Controlled degassing at Lake Nyos since 2001 has also reduced the CO 2 content. It is currently slightly below the level estimated after the limnic eruption in 1986. However, the current CO 2 content still amounts to 80% of the maximum level of 14.8 giga moles observed in January 2001. The depth of the lower chemocline may reach the pipe intake depth of 203 m within a few years. After this situation is reached the degassing rate with the current system will progressively decline, and it would take decades to remove the majority of dissolved gases even if the degassing system keeps working continuously. Additional degassing pipes must be installed to speed up gas removal from Lake Nyos in order to make the area safer for local populations.

Lake Monoun, Lake Nyos↗

Use of partial dissolution techniques in geochemical exploration

Application of partial dissolution techniques to geochemical exploration has advanced from an early empirical approach to an approach based on sound geochemical principles. This advance assures a prominent future position for the use of these techniques in geochemical exploration for concealed mineral deposits. Partial dissolution techniques are classified as single dissolution or sequential multiple dissolution depending on the number of steps taken in the procedure, or as “nonselective” extraction and as “selective” extraction in terms of the relative specificity of the extraction. The choice of dissolution techniques for use in geochemical exploration is dictated by the geology of the area, the type and degree of weathering, and the expected chemical forms of the ore and of the pathfinding elements. Case histories have illustrated many instances where partial dissolution techniques exhibit advantages over conventional methods of chemical analysis used in geochemical exploration.

Journal of Geochemical Exploration↗

Response of douglas fir (Pseudotsuga menziesii) to uraniferous groundwater in a small glaciated drainage, Northeastern Washington State

Douglas fir trees and associated soils were sampled from the slopes of a small (∼4 km 2 ) drainage basin in northeastern Washington to investigate the biogeochemical response to locally uraniferous groundwater. Uranium is preferentially incorporated in needles and twigs compared to larger branches or the trunk. The U concentration in needle ash ranges from 0.2 to 5.8μg g −1 (ppm) and shows no correlation with the U concentration in associated soils. Rather, the distribution of anomalously uraniferous douglas fir (> 1.0 μ g g −1 U in needle ash) appears to be controlled by observed or readily inferred pathways of near-surface groundwater movement in the drainage. These pathways include: (1) general downslope movement of subsurface runoff; (2) increased flux of near-surface groundwater near the toe of an alluvial fan; and (3) emergence of uraniferous (100–150 ng ml −1 [ppb] groundwater in the vicinity of a slope spring. The data also indicate the presence of near-surface uraniferous groundwater along a structurally controlled zone that parallels the north-south strike of the valley, and that includes the slope spring. The results suggest that biogeochemical sampling may be used to supplement more direct, but more limited, measurements of groundwater quality and flow regime in areas of near-surface contaminated groundwater.

Journal of Geochemical Exploration↗

The role of atomic absorption spectrometry in geochemical exploration

In this paper we briefly describe the principles of atomic absorption spectrometry (AAS) and the basic hardware components necessary to make measurements of analyte concentrations. Then we discuss a variety of methods that have been developed for the introduction of analyte atoms into the light path of the spectrophotometer. This section deals with sample digestion, elimination of interferences, and optimum production of ground-state atoms, all critical considerations when choosing an AAS method. Other critical considerations are cost, speed, simplicity, precision, and applicability of the method to the wide range of materials sampled in geochemical exploration. We cannot attempt to review all of the AAS methods developed for geological materials but instead will restrict our discussion to some of those appropriate for geochemical exploration. Our background and familiarity are reflected in the methods we discuss, and we have no doubt overlooked many good methods. Our discussion should therefore be considered a starting point in finding the right method for the problem, rather than the end of the search. Finally, we discuss the future of AAS relative to other instrumental techniques and the promising new directions for AAS in geochemical exploration.

Journal of Geochemical Exploration↗

A procedure for estimating Bacillus cereus spores in soil and stream-sediment samples — A potential exploration technique

The presence of bacterial spores of the Bacillus cereus group in soils and stream sediments appears to be a sensitive indicator of several types of concealed mineral deposits, including vein-type gold deposits. The B. cereus assay is rapid, inexpensive, and inherently reproducible. The test, currently under investigation for its potential in mineral exploration, is recommended for use on a research basis. Among the aerobic spore-forming bacilli, only B. cereus and closely related strains produce an opaque zone in egg-yolk emulsion agar. This characteristic, also known as the Nagler of lecitho-vitellin reaction, has long been used to rapidly indentify and estimate presumptive B. cereus . The test is here adapted to permit rapid estimation of B. cereus spores in soil and stream-sediment samples. Relative standard deviation was 10.3% on counts obtained from two 40-replicate pour-plate determinations. As many as 40 samples per day can be processed. Enough procedural detail is included to permit investigation of the test in conventional geochemical laboratories using standard microbiological safety precautions.

Journal of Geochemical Exploration↗

Movement of elements into the atmosphere from coniferous trees in subalpine forests of Colorado and Idaho

Exudates from conifer trees, presumably consisting largely of volatile materials, were sampled at 19 subalpine localitites in Colorado and Idaho where anomalous amounts of several metals were determined in vegetation and mull during previous geochemical testing. The trees sampled were lodgepole pine ( Pinus contorta ), Engelmann spruce ( Picea engelmannii ) and Douglas fir ( Pseudotsuga menziesii ). The condensed exudates were passed through No. 40 Whatman filters, and through 5-micron, 0.45-micron, and 0.05-micron average-pore-diameter membrane filters, evaporated to dryness, and each residue was ashed and analyzed by a semiquantitative spectrographic method. The ashed residues of the exudates contain lithium, beryllium, boron, sodium, magnesium, titanium, vanadium, chromium, manganese, iron, cobalt, nickel, copper, zinc, gallium, arsenic, strontium, yttrium, zirconium, molybdenum, silver, lead, bismuth, cadmium, tin, antimony, barium, and lanthanum. The presence of these elements suggests that volatile exudates from vegetation are a medium for the transport of elements in the biogeochemical cycle in subalpine environments. Thus, air sampling and analysis of aerosols derived from volatile exudates may be a useful tool in geochemical exploration.

Colorado, Idaho↗

Adjustment of geochemical background by robust multivariate statistics

Conventional analyses of exploration geochemical data assume that the background is a constant or slowly changing value, equivalent to a plane or a smoothly curved surface. However, it is better to regard the geochemical background as a rugged surface, varying with changes in geology and environment. This rugged surface can be estimated from observed geological, geochemical and environmental properties by using multivariate statistics.

Journal of Geochemical Exploration↗

A geochemical sampling technique for use in areas of active alpine glaciation: an application from the central Alaska Range

In mountainous regions containing extensive glacier systems there is a lack of suitable material for conventional geochemical sampling. As a result, in most geochemical sampling programs a few stream-sediment samples collected at, or near, the terminus of valley glaciers are used to evaluate the mineral potential of the glaciated area. We have developed and tested a technique which utilizes the medial moraines of valley glaciers for systematic geochemical exploration of the glacial catchment area. Moraine sampling provides geochemical information that is site-specific in that geochemical anomalies can be traced directly up-ice to bedrock sources. Traverses were made across the Trident and Susitna glaciers in the central Alaska Range where fine-grained (clay to sand size) samples were collected from each medial moraine. These samples were prepared and chemically analyzed to determine the concentration of specific elements. Fifty pebbles were collected at each moraine for archival purposes and for subsequent lithologic identification. Additionally, fifty cobbles and fifty boulders were examined and described at each sample site to determine the nature and abundance of lithologies present in the catchment area, the extent and nature of visible mineralization, the presence and intensity of hydrothermal alteration and the existence of veins, dikes and other minor structural features. Results from the central Alaska Range have delineated four distinct multi-element anomalies which are a response to potential mineralization up-ice from the medial moraine traverse. By integrating the lithologic, mineralogical and geochemical data the probable geological setting of the geochemical anomalies is determined.

Journal of Geochemical Exploration↗

Multiple gas analyses using a mobile mass spectrometer

A truck-mounted mass-spectrometer gas analyzer is described and field examples of its use are given. This unit provides a gas analyzer that can be used in the field to rapidly analyze a large number of gases. It has enabled us to establish that gas anomalies occur over a variety of deposit types and in different environments. Gases may prove to be useful geochemical indicators in exploration for concealed mineral deposits.

Journal of Geochemical Exploration↗

Geochemical exploration for copper-nickel deposits in the cool-humid climate of northeastern Minnesota

Water was used as a medium for geochemical exploration to detect copper-nickel mineralization along the basal zone of the Duluth Complex. Ni 2+ is the most important pathfinder for the detection of the mineralized rocks, followed by Cu 2+ and SO 4 2− and to a lesser extent Mg 2+ and SiO 2 . A normalized sum plot using these species defines the mineralization more consistently than a single-element plot, mainly because the absence of one variable does not significantly influence the normalized sum value. A hydrogeochemical survey was conducted in an area of known copper-nickel mineralization in the cool-humid climate of northeastern Minnesota. The area is covered with glacial drift, and wetlands are abundant. Modeling of the chemistry of waters indicates that the waters are oxidizing and have a pH of 7 or less. The most important pathfinder species in the waters, Cu 2+ , Ni 2+ , and SO 4 2− , are derived from the simple weathering of sulfide minerals and are mobile in the waters in this environment. Plots of Cu and Ni concentrations in soils show that Cu followed by Ni are the most useful indicator elements for delineating copper-nickel mineralization. The ability of soils and water to delineate the mineralization supports the use of both media for geochemical exploration in this cool-humid environment. In the wetlands, abundant water is available and soils are scarce or absent; where soils are abundant, waters are generally scarce or absent. The use of both media is recommended for geochemical exploration in this environment.

Journal of Geochemical Exploration↗