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Minor-element and Sr-isotope geochemistry of tertiary stocks, Colorado mineral belt

Rocks of the northeast portion of the Colorado mineral belt form two petrographically, chemically and geographically distinct rock suites: (1) a silica oversaturated granodiorite suite; and (2) a silica saturated, high alkali monzonite suite. Rocks of the granodiorite suite generally have Sr contents less than 1000 ppm, subparallel REE patterns and initial 87Sr/ 86Sr ratios greater than 0.707. Rocks of the monzonite suite are restricted to the northeast part of the mineral belt, where few rocks of the granodiorite suite occur, and generally have Sr contents greater than 1000 ppm, highly variable REE patterns and 87Sr/86Sr initial ratios less than 0.706. Despite forming simple, smooth trends on major element variation diagrams, trace element data for rocks of the granodiorite suite indicate that they were not derived from a single magma. These rocks were derived from magmas having similar REE patterns, but variable Rb and Sr contents, and Rb/Sr ratios. The preferred explanation for these rocks is that they were derived by partial melting of a mixed source, which yielded pyroxene granulite or pyroxenite residues. The monzonite suite is chemically and petrographically more complex than the granodiorite suite. It is subdivided here into alkalic and mafic monzonites, and quartz syenites, based on the textural relations of their ferromagnesian phases and quartz. The geochemistry of these three rock types require derivation from separate and chemically distinct magma types. The preferred explanation for the alkalic monzonites is derivation from a heterogeneous mafic source, leaving a residue dominated by garnet and clinopyroxene. Early crystallization of sphene from these magmas was responsible for the severe depletion of the REE observed in the residual magmas. The lower Sr content and higher Rb/Sr ratios of the mafic monzonites requires a plagioclase-bearing source. The Sr-isotope systematics of the majority of these rocks are interpreted to be largely primary, and not the result of crustal contamination. The positive correlation of Rb/Sr and 87Sr/86Sr ratios for the least fractionated samples indicate that the sources from which parent magmas of both the granodiorite and monzonite suites were derived are Precambrian in age. ?? 1978 Springer-Verlag.

Contributions to Mineralogy and Petrology

Trace elements and organochlorines in the shoalgrass community of the lower Laguna Madre Texas

Our objectives were to measure concentrations of seven trace elements and 14 organochlorine compounds in sediment and biota of the shoalgrass ( Halodule wrightii ) community of the lower Laguna Madre of south Texas and to determine whether chemicals associated with agriculture (e.g. mercury, arsenic, selenium, organochlorine pesticides) were highest near agricultural drainages. Arsenic, mercury, selenium, lead, cadmium, and organochlorines were generally at background concentrations throughout the lower Laguna Madre. Nickel and chromium concentrations were exceptionally high in shrimp and pinfish ( Lagodon rhomboides ), which is difficult to explain because of no known anthropogenic sources for these trace elements. For sediment and blue crabs ( Callinectes sapidus ), mercury was highest near agricultural drainages. Also, DDE was more frequently detected in blue crabs near agricultural drainages than farther away. In contrast, selenium concentrations did not differ among collecting sites and arsenic concentrations were lowest in shoalgrass, blue crabs, and brown shrimp ( Penaeus aztecus ) near agricultural drainages.

Texas

The effect of membrane filtration on dissolved trace element concentrations

The almost universally accepted operational definition for dissolved constituents is based on processing The almost universally accepted operational definition for dissolved constituents is based on processing whole-water samples through a 0.45-μm membrane filter. Results from field and laboratory experiments indicate that a number of factors associated with filtration, other than just pore size (e.g., diameter, manufacturer, volume of sample processed, amount of suspended sediment in the sample), can produce substantial variations in the ‘disolved’ concentrations of such elements as Fe, Al, Cu, Zn, Pb, Co, and Ni. These variations result from the inclusion/exclusion of colloidally-associated trace elements. Thus, 'dissolved' concentrations quantitated by analyzing filtrates generated by processing whole-water through similar pore-sized membrane filters may not be equal/comparable. As such, simple filtration through a 0.45-μm membrane filter may no longer represent an acceptable operational definition for dissolved chemical constituents. This conclusion may have important implications for environmental studies and regulatory agencies.

Water, Air, & Soil Pollution

Accumulation of trace elements, pesticides, and polychlorinated biphenyls in sediments and the clam Corbicula manilensis of the Apalachicola River, Florida

A survey of trace element and synthetic organic compound concentrations in bottom materials was conducted on the Apalachicola River in northwest Florida in 1979–80 as part of the Apalachicola River Quality Assessment. Substances analyzed included trace elements (predominantly heavy metals), organochlorine insecticides, organophosphorus insecticides, chlorinated phenoxy-acid herbicides, and poly chlorinated biphenyls (PCBs). Three kinds of materials were surveyed: finegrained sediments, whole-body tissue of the Asiatic clam Corbicula manilensis , and bottom-load organic detritus. No hazardous levels of any of the substances were found. Concentrations in the finegrained sediments and clams were generally at least ten times lower than maximum limits considered safe for biota of aquatic systems. A comparison of trace-substance data from the Apalachicola River with data from Lake Seminole (upstream) and Apalachicola Bay (downstream) showed lower concentrations in riverine clams. Sediment concentrations in all parts of the system were comparable. Most trace substances in the Apalachicola River enter the river from the upstream part of the basin (the Chattahoochee and Flint Rivers in Georgia and Alabama) and from nonpoint sources throughout the basin. There are no major point discharges along the Apalachicola. Trend analysis was limited by the scope of the study, but did not reveal any spatial or temporal trends in concentrations of any of the substances analyzed. Concentrations of organic compounds and most metals in Corbicula manilensis did not correlate with those in sediments.

Florida

Selenium and other elements in juvenile striped bass from the San Joaquin Valley and San Francisco Estuary, California

Concentrations of selenium and other trace elements were determined in 55 whole body samples of juvenile anadromous striped bass ( Morone saxatilis ) from the San Joaquin Valley and San Francisco Estuary, California. The fish (≤1 yr old—the predominant life stage in the San Joaquin Valley) were collected in September–December 1986 from 19 sites in the Valley and 3 sites in the Estuary, and analyzed for the following elements: aluminum (Al), arsenic (As), boron (B), barium (Ba), beryllium (Be), cadmium (Cd), chromium (Cr), copper (Cu), iron (Fe), mercury (Hg), magnesium (Mg), molybdenum (Mo), nickel (Ni), lead (Pb), selenium (Se), strontium (Sr), vanadium (V), and zinc (Zn). When compared to concentrations in whole freshwater fish measured by surveys from other waters, a few samples contained higher levels, of As, Cd, Cu, Pb, and Se. The median concentrations of Al, As, Cu, Fe, Mg, Se, and Sr also differed significantly ( P ⩽0.05) among sites. However, only Se concentrations were highest (up to 7.9 μg/g dry weight) in samples from Valley sites exposed to agricultural subsurface (tile) drainwater; concentrations were lower in samples collected elsewhere. Water quality variables—especially those strongly influenced by tile drainwater (conductivity, total dissolved solids, total alkalinity, and total hardness)—were also significantly correlated ( P ⩽0.05) with Se concentrations in fish. Selenium concentrations in striped bass from the Estuary were only one-fourth to one-half the concentrations measured in the most contaminated fish from the San Joaquin River.

California

Report of the IAU Working Group on Cartographic Coordinates and Rotational Elements of the Planets and Satellites

This paper is the entire report of the IAU Working Group on Cartographic Coordinates and Rotational Elements of the Planets and Satellites, including three annexes. Tables give the recemmended values for the directions of the north poles of rotation and the prime meridians of the planets and satellites. Reference surfaces for mapping these bodies are described. The annexes discuss the guiding principles, given in the body of the report, present explanatory notes, and provide a bibliography of the rotational elements and reference surfaces of the planets and satellites, definitions, and algebraic expressions of relevant parameters. ?? 1980 D. Reidel Publishing Co.

Celestial Mechanics

Survey of trace elements in coals and coal-related materials by neutron activation analysis

Utilizing primarily instrumental neutron activation analysis (INAA) and other analytical methods as many as 61 elements were quantitatively surveyed in 170 U.S. whole coals, 70 washed coals, and 40 bench samples. Data on areal and vertical distributions in various regions were obtained along with extensive information on the mode of occurrence of various elements in the coal matrix itself. ?? 1977 Akade??miai Kiado??.

Journal of Radioanalytical Chemistry

Magma mixing and the generation of isotopically juvenile silicic magma at Yellowstone caldera inferred from coupling 238 U– 230 Th ages with trace elements and Hf and O isotopes in zircon and Pb isotopes in sanidine

The nature of compositional heterogeneity within large silicic magma bodies has important implications for how silicic reservoirs are assembled and evolve through time. We examine compositional heterogeneity in the youngest (~170 to 70 ka) post-caldera volcanism at Yellowstone caldera, the Central Plateau Member (CPM) rhyolites, as a case study. We compare 238 U– 230 Th age, trace-element, and Hf isotopic data from zircons, and major-element, Ba, and Pb isotopic data from sanidines hosted in two CPM rhyolites (Hayden Valley and Solfatara Plateau flows) and one extracaldera rhyolite (Gibbon River flow), all of which erupted near the caldera margin ca. 100 ka. The Hayden Valley flow hosts two zircon populations and one sanidine population that are consistent with residence in the CPM reservoir. The Gibbon River flow hosts one zircon population that is compositionally distinct from Hayden Valley flow zircons. The Solfatara Plateau flow contains multiple sanidine populations and all three zircon populations found in the Hayden Valley and Gibbon River flows, demonstrating that the Solfatara Plateau flow formed by mixing extracaldera magma with the margin of the CPM reservoir. This process highlights the dynamic nature of magmatic interactions at the margins of large silicic reservoirs. More generally, Hf isotopic data from the CPM zircons provide the first direct evidence for isotopically juvenile magmas contributing mass to the youngest post-caldera magmatic system and demonstrate that the sources contributing magma to the CPM reservoir were heterogeneous in 176 Hf/ 177 Hf at ca. 100 ka. Thus, the limited compositional variability of CPM glasses reflects homogenization occurring within the CPM reservoir, not a homogeneous source.

Wyoming

Unravelling the complexity of magma plumbing at Mount St. Helens: A new trace element partitioning scheme for amphibole

Volcanoes at subduction zones reside above complex magma plumbing systems, where individual magmatic components may originate and interact at a range of pressures. Because whole-rock compositions of subduction zone magmas are the integrated result of processes operating throughout the entire plumbing system, processes such as mixing, homogenisation and magma assembly during shallow storage can overprint the chemical signatures of deeper crustal processes. Whereas melt inclusions provide an effective way to study the uppermost 10–15 km of the plumbing system, challenges remain in understanding magma intrusion, fractionation and hybridisation processes in the middle to lower crust (15–30 km depth), which commonly involves amphibole crystallisation. Here, we present new insights into the mid-crustal plumbing system at Mount St. Helens, USA, using multiple regression methods to calculate trace element partition coefficients for amphibole phenocrysts, and thus infer the trace element compositions of their equilibrium melts. The results indicate vertically distributed crystal fractionation, dominated by amphibole at higher pressures and in intermediate melts, and by plagioclase at lower pressures. Variations in Nb, Zr and REE concentrations at intermediate SiO 2 contents suggest repeated scavenging of partially remelted intrusive material in the mid-crust, and mixing with material from geochemically diverse sources. Amphibole is an effective probe for deep crustal magmatism worldwide, and this approach offers a new tool to explore the structure and chemistry of arc magmas, including those forming plutonic or cumulate materials that offer no other constraints on melt composition.

Contributions to Mineralogy and Petrology

Sphene and zircon in the Highland Range volcanic sequence (Miocene, southern Nevada, USA): Elemental partitioning, phase relations, and influence on evolution of silicic magma

Sphene is prominent in Miocene plutonic rocks ranging from diorite to granite in southern Nevada, USA, but it is restricted to rhyolites in coeval volcanic sequences. In the Highland Range volcanic sequence, sphene appears as a phenocryst only in the most evolved rocks (72–77 mass% SiO 2 ; matrix glass 77–78 mass% SiO 2 ). Zr-in-sphene temperatures of crystallization are mostly restricted to 715 and 755°C, in contrast to zircon (710–920°C, Ti-in-zircon thermometry). Sphene rim/glass Kds for rare earth elements are extremely high (La 120, Sm 1200, Gd 1300, Lu 240). Rare earth elements, especially the middle REE (MREE), decrease from centers to rims of sphene phenocrysts along with Zr, demonstrating the effect of progressive sphene fractionation. Whole rocks and glasses have MREE-depleted, U-shaped REE patterns as a consequence of sphene fractionation. Within the co-genetic, sphene-rich Searchlight pluton, only evolved leucogranites show comparable MREE depletion. These results indicate that sphene saturation in intruded and extruded magmas occurred only in highly evolved melts: abundant sphene in less silicic plutonic rocks represents a late-stage ‘bloom’ in fractionated interstitial melt.

Nevada

Nitrogen-bedrock interactions regulate multi-element nutrient limitation and sustainability in forests

Nutrient limitation of tree growth can intensify when nutrients are lost to forest harvest, creating challenges for forest growth and sustainability. Forest harvest accelerates nutrient loss by removing nutrient-containing biomass and by increasing nutrient leaching, shaping patterns of nutrient depletion that cause long-term shifts in nutrient limitation. Nitrogen most frequently limits tree growth, but where nitrogen is abundant, nutrient limitation often shifts to phosphorus and base cations, depending on soil mineralogy. We used the process-based biogeochemical model NutsFor to evaluate how multiple elements can limit long-term forest growth via interactions between soil nitrogen (low vs. high nitrogen) and soil mineralogy (sedimentary vs. basaltic bedrock). Simulations were run for 525 years with 40-year harvest intervals for managed Douglas-fir forests of the Oregon Coast Range. In low nitrogen sites, nutrient limitation switched after several centuries from nitrogen to phosphorus, as cycles of forest growth and harvest depleted soil organic phosphorus pools. In contrast, high nitrogen sites displayed severe base cation depletion and reduced tree growth within only one to two rotations, with sedimentary bedrock sites limited by calcium and basaltic sites by both calcium and potassium. Harvesting stimulated the largest fractional losses of nitrogen and potassium across all simulations, and additionally of calcium in high nitrogen sites. These multi-element simulations of interactions among harvesting, soil nitrogen, and bedrock type provide a set of testable predictions to guide monitoring and changes in management aimed at sustaining long-term forest productivity across a wide range of soil biogeochemical conditions.

Biogeochemistry

Radionuclides, trace elements, and radium residence in phosphogypsum of Jordan

Voluminous stockpiles of phosphogypsum (PG) generated during the wet process production of phosphoric acid are stored at many sites around the world and pose problems for their safe storage, disposal, or utilization. A major concern is the elevated concentration of long-lived 226Ra (half-life = 1,600 years) inherited from the processed phosphate rock. Knowledge of the abundance and mode-of-occurrence of radium (Ra) in PG is critical for accurate prediction of Ra leachability and radon (Rn) emanation, and for prediction of radiation-exposure pathways to workers and to the public. The mean (??SD) of 226Ra concentrations in ten samples of Jordan PG is 601 ?? 98 Bq/kg, which falls near the midrange of values reported for PG samples collected worldwide. Jordan PG generally shows no analytically significant enrichment (< 10%) of 226Ra in the finer (< 53 ??m) grain size fraction. Phosphogypsum samples collected from two industrial sites with different sources of phosphate rock feedstock show consistent differences in concentration of 226Ra and rare earth elements, and also consistent trends of enrichment in these elements with increasing age of PG. Water-insoluble residues from Jordan PG constitute <10% of PG mass but contain 30-65% of the 226Ra. 226Ra correlates closely with Ba in the water-insoluble residues. Uniformly tiny (< 10 ??m) grains of barite (barium sulfate) observed with scanning electron microscopy have crystal morphologies that indicate their formation during the wet process. Barite is a well-documented and efficient scavenger of Ra from solution and is also very insoluble in water and mineral acids. Radium-bearing barite in PG influences the environmental mobility of radium and the radiation-exposure pathways near PG stockpiles. ?? 2010 US Government.

Environmental Geochemistry and Health

Addressing foundational elements of regional land-use change forecasting

Regional land-use models must address several foundational elements, including understanding geographic setting, establishing regional land-use histories, modeling process and representing drivers of change, representing local land-use patterns, managing issues of scale and complexity, and development of scenarios. Key difficulties include managing an array of biophysical and socioeconomic processes across multiple spatial and temporal scales, and acquiring and utilizing empirical data to support the analysis of those processes. The Southeastern and Pacific Northwest regions of the United States, two heavily forested regions with significant forest industries, are examined in the context of these foundational elements. Geographic setting fundamentally affects both the primary land cover (forest) in the two regions, and the structure and form of land use (forestry). Land-use histories of the regions can be used to parameterize land-use models, validate model performance, and explore land-use scenarios. Drivers of change in the two regions are many and varied, with issues of scale and complexity posing significant challenges. Careful scenario development can be used to simplify process-based land-use models, and can improve our ability to address specific research questions. The successful modeling of land-use change in these two areas requires integration of both top-down and bottom-up drivers of change, using scenario frameworks to both guide and simplify the modeling process. Modular approaches, with utilization and integration of existing process models, allow regional land-use modelers the opportunity to better represent primary drivers of land-use change. However, availability of data to represent driving forces remains a primary obstacle.

Landscape Ecology

Assessment of trace element accumulation by earthworms in an orchard soil remediation study using soil amendments

This study assessed potential bioaccumulation of various trace elements in grasses and earthworms as a consequence of soil incorporation of organic amendments for in situ remediation of an orchard field soil contaminated with organochlorine and Pb pesticide residues. In this experiment, four organic amendments of differing total organic carbon content and quality (two types of composted manure, composted biosolids, and biochar) were added to a contaminated orchard field soil, planted with two types of grasses, and tested for their ability to reduce bioaccumulation of organochlorine pesticides and metals in earthworms. The experiment was carried out in 4-L soil microcosms in a controlled environment for 90 days. After 45 days of orchardgrass or perennial ryegrass growth, Lumbricus terrestris L. were introduced to the microcosms and exposed to the experimental soils for 45 days before the experiment was ended. Total trace element concentrations in the added organic amendments were below recommended safe levels and their phytoavailablity and earthworm availability remained low during a 90-day bioremediation study. At the end of the experiment, total tissue concentrations of Cu, Cd, Mn, Pb, and Zn in earthworms and grasses were below recommended safe levels. Total concentrations of Pb in test soil were similar to maximum background levels of Pb recorded in soils in the Eastern USA (100 mg kg −1 d.w.) because of previous application of orchard pesticides. Addition of aged dairy manure compost and presence of grasses was effective in reducing the accumulation of soil-derived Pb in earthworms, thus reducing the risk of soil Pb entry into wildlife food chains.

Maryland

Hydrologic compartmentalization and analytic-element groundwater-flow simulations for a draining mine tunnel

Draining mine tunnels contribute contaminants to groundwater and surface water, but remediation strategies may be hindered as hydrogeologic characterization and modeling of these heterogeneous features generally relies on sparse data sets. The Captain Jack mine site in Colorado, USA, presents a unique data set allowing for temporal evaluation of groundwater connectivity in the vicinity of an abandoned mine, where a hydraulic bulkhead is impounding water within the mine workings. This study applied statistical analysis of system pressure responses to bulkheading and used an analytic-element modeling approach to characterize heterogeneity and groundwater flow. Groundwater-level elevation data collected over a period of 4 years, both prior to and after bulkheading, indicate that the mine workings act as a sink to the local groundwater system. Despite groundwater flow being generally oriented towards the mine workings, there are also large vertical and horizontal hydraulic gradients which persist through time. Although the groundwater system is highly compartmentalized, statistical analysis using Kendall’s Tau indicates correlations between hydraulic head changes in the mine workings and several wells completed in crystalline bedrock, indicating the influence of fracture flow. An analytic-element model was parameterized to account for uncertainty in hydraulic conductivity, recharge, and discharge. Model results reproduced the range of observed hydraulic heads in the mine workings and adjacent igneous dikes but failed to closely simulate hydraulic heads in several wells located distal from the mine workings in granitic bedrock. The modeling approach shows potential promise, however, for conducting preliminary modeling to guide data collection at other similar mine sites.

Colorado

Volcanism in the Sumisu Rift, I. Major element, volatile, and stable isotope geochemistry

A bimodal volcanic suite with K Ar ages of 0.05–1.40 Ma was collected from the Sumisu Rift using alvin . These rocks are contemporaneous with island arc tholeiite lavas of the Izu-Ogasawara arc 20 km to the east, and provide a present day example of volcanism associated with arc rifting and back-arc basin initiation. Major element geochemistry of the basalts is most similar to that of basalts found in other, more mature back-arc basins, which indicates that back-arc basins need not begin their magmatic evolution with lavas bearing strong arc signatures. Volatile concentrations distinguish Sumisu Rift basalts from island arc basalts and MORB. H 2 O contents, which are at least four times greater than in MORB, suppress plagioclase crystallization. This suppression results in a more mafic fractionating assemblage, which prevents Al 2 O 3 depletion and delays the initiation of Fe 2 O 3 (tot) and TiO 2 enrichment. However, unlike arc basalts,Fe 3+/ ΣFe ratios are only slightly higher than in MORB and are insufficient to cause magnetite saturation early enough to suppress Fe 2 O 3 (tot) and TiO 2 enrichment. Thus, major element trends are more similar to those of MORB than arcs. H 2 O, CO 2 and S are undersaturated relative to pure phase solubility curves, indicating exsolution of an H 2 O-rich mixed gas phase. HighH 2 O/S, highδD, and low (MORB-like)δ 34 S ratios are considered primary and distinctive of the back-arc basin setting.

Earth and Planetary Science Letters

Trace element evaluation of a suite of rocks from Reunion Island, Indian Ocean

Reunion Island consists of an olivine-basalt shield capped by a series of flows and intrusives ranging from hawaiite through trachyte. Eleven rocks representing the total compositional sequence have been analyzed for U, Th and REE. Eight of the rocks (group 1) have positive-slope, parallel, chondrite-normalized REE fractionation patterns. Using a computer model, the major element compositions of group 1 whole rocks and observed phenocrysts were used to predict the crystallization histories of increasingly residual liquids, and allowed semi-quantitative verification of origin by fractional crystallization of the olivine-basalt parent magma. Results were combined with mineral-liquid distribution coefficient data to predict trace element abundances, and existing data on Cr, Ni, Sr and Ba were also successfully incorporated in the model. The remaining three rocks (group 2) have nonuniform positive-slope REE fractionation patterns not parallel to group 1 patterns. Rare earth fractionation in a syenite is explained by partial melting of a source rich in clinopyroxene and/or hornblende. The other two rocks of group 2 are explained as hybrids resulting from mixing of syenite and magmas of group 1.

Geochimica et Cosmochimica Acta

Volatilization, transport and sublimation of metallic and non-metallic elements in high temperature gases at Merapi Volcano, Indonesia

Condensates, silica tube sublimates and incrustations were sampled from 500–800°C fumaroles and lava samples were collected at Merapi Volcano, Indonesia in Jan.–Feb., 1984. With respect to the magma, Merapi gases are enriched by factors greater than 10 5 in Se, Re, Bi and Cd; 10 4 –10 5 in Au, Br, In, Pb and W; 10 3 –10 4 in Mo, Cl, Cs, S, Sn and Ag; 10 2 –10 3 in As, Zn, F and Rb; and 1–10 2 in Cu, K, Na, Sb, Ni, Ga, V, Fe, Mn and Li. The fumaroles are transporting more than 10 6 grams/day ( g d "> gd ) of S, Cl and F; 10 4 –10 6 g/d of Al, Br, Zn, Fe, K and Mg; 10 3 –10 4 g d "> gd of Pb, As, Mo, Mn, V, W and Sr; and less than 10 3 g d "> gd of Ni, Cu, Cr, Ga, Sb, Bi, Cd, Li, Co and U. With decreasing temperature (800-500°C) there were five sublimate zones found in silica tubes: 1) cristobalite and magnetite (first deposition of Si, Fe and Al); 2) K-Ca sulfate, acmite, halite, sylvite and pyrite (maximum deposition of Cl, Na, K, Si, S, Fe, Mo, Br, Al, Rb, Cs, Mn, W, P, Ca, Re, Ag, Au and Co); 3) aphthitalite (K-Na sulfate), sphalerite, galena and Cs-K. sulfate (maximum deposition of Zn, Bi, Cd, Se and In; higher deposition of Pb and Sn); 4) Pb-K chloride and Na-K-Fe sulfate (maximum deposition of Pb, Sn and Cu); and 5) Zn, Cu and K-Pb sulfates (maximum deposition of Pb, Sn, Ti, As and Sb). The incrustations surrounding the fumaroles are also chemically zoned. Bi, Cd, Pb, W, Mo, Zn, Cu, K, Na, V, Fe and Mn are concentrated most in or very close to the vent as expected with cooling, atmospheric contamination and dispersion. The highly volatile elements Br, Cl, As and Sb are transported primarily away from high temperature vents. Ba, Si, P, Al, Ca and Cr are derived from wall rock reactions. Incomplete degassing of shallow magma at 915°C is the origin of most of the elements in the Merapi volcanic gas, although it is partly contaminated by particles or wall rock reactions. The metals are transported predominantly as chloride species. As the gas cools in the fumarolic environment, it becomes saturated with sublimate phases that fractionate from the gas in the order of their equilibrium saturation temperatures. Devolatilization of a cooling batholith could transport enough acids and metals to a hydrothermal system to play a significant role in forming an ore deposit. However, sublimation from a high temperature, high velocity carrier gas is not efficient enough to form a large ore deposit. Re, Se, Cd and Bi could be used as supporting evidence for magmatic fluid transport in an ore deposit.

Geochimica et Cosmochimica Acta