Search USGS⌕ Search

Geology topics

C. A. Johnson

Publications and source records attributed to C. A. Johnson.

30 records · Page 2Linked to original sources
USGS2001

Use of 17 O/ 16 O to trace atmospherically-deposited sulfate in surface waters: A case study in alpine watersheds in the Rocky Mountains

Building on the discovery of excess 17 O in atmospheric sulfate by Lee et al. (2001), we have carried out a case study to determine whether 17 O might provide a new tool for quantifying the impact of atmospheric deposition on surface-water sulfate loads. In Rocky Mountain alpine regions, excess 17 O was found to be characteristics of atmospheric sulfate deposited in snow. Excess 17 O was also evident in stream sulfate in one of two high-elevation watersheds where analyses were made. Isotope mass balance calculations gave surprizingly low atmospheric contributions to stream sulfate suggesting that (1) despite abundant outcrop and sparse soil in these areas, significant sulfate may be taken up and released by soil microbes before being exported in streams, and (2) surface waters can carry multiple non-atmospheric sulfate types, some possibly anthropogenic. Measurements of 17 O may prove very useful in studies of sulfate behavior in a variety of surficial environments.

Geophysical Research Letters↗
USGS2001

On-line sulfur isotope analysis of organic material by direct combustion: Preliminary results and potential applications

Sulfur isotopes have received little attention in ecology studies because plant and animal materials typically have low sulfur concentrations (< 1 wt.%) necessitating labor-intensive chemical extraction prior to analysis. To address the potential of direct combustion of organic material in an elemental analyzer coupled with a mass spectrometer, we compared results obtained by direct combustion to results obtained by sulfur extraction with Eschka's mixture. Direct combustion of peat and animal tissue gave reproducibility of better than 0.5??? and on average, values are 0.8??? higher than values obtained by Eschka extraction. Successful direct combustion of organic material appears to be a function of sample matrix and sulfur concentration. Initial results indicate that direct combustion provides fast, reliable results with minimal preparation. Pilot studies underway include defining bear diets and examining fluctuations between freshwater and brackish water in coastal environments.

Isotopes in Environmental and Health Studies↗
USGS2001

Sources of salinity near a coal mine spoil pile, north-central Colorado

A small (1 km 2 ) salt-affected stream drainage on the High Plains north of Denver, Colorado was sampled to determine the near-surface dispersion of soluble salts and metals from low-sulfur coal mining waste (spoil). Surface waters collected along the 0.8-km stream reach, and aqueous leachates of spoil and naturally saline local soil, were analyzed for chemical constituents and sulfur isotopes. In this semiarid setting with abundant carbonate-bearing surficial sediments, the limited, mildly acidic drainage from the spoil pile is quickly neutralized, restricting the mobility of many elements. However, some spoil-derived constituents were clearly traceable within the upper 0.4 km of the stream reach. Spoil leachates and surface water near the spoil pile have distinctive compositions of major anions and cations, and elevated levels of dissolved nitrate compared with downstream waters. Spoil-derived sulfate was traceable because it has generally positive values of δ 34 S that contrasted with generally negative values of δ 34 S in soil leachates and evaporite salts from the surrounding area. Spatial–chemical sampling of surface water showed an abrupt increase in dissolved U, Se, B, Li, and Mn in the lower 0.4 km of the stream reach where shallow ground water from surrounding irrigated fields contributed to surface flow. The downstream evolution of surface water chemistry and sulfur isotopic composition is consistent with mixing between spoil-affected upstream water and irrigation-return water. The methods described should be applicable at other sites in similar settings where the environmental effect of low-sulfur coal mining waste must be assessed and where access to samples of shallow ground water is limited.

Colorado↗
USGS1999

Syngenetic Au on the Carlin trend: Implications for Carlin-type deposits

A new type of gold occurrence recently discovered in the Carlin trend, north-central Nevada, is clearly distinct from classic Carlin-type gold ore. These occurrences are interpreted to be of sedimentary exhalative (sedex) origin because they are stratiform and predate compaction and lithification of their unaltered Devonian host rocks. They contain barite that exhibits δ 34 S and δ 18 0 values identical to sulfate in Late Devonian seawater and sedex-type barite deposits. Abrupt facies changes in the host rocks strongly suggest synsedimentary faulting and foundering of the carbonate shelf during mineralization, as is characteristic of sedex deposits. Gold occurs both as native inclusions in synsedimentary base-metal sulfides and barite, and as chemical enrichments in sulfide minerals. The absence of alteration and lack of δ 13 C and δ 18 0 isotopic shift of primary carbonates in these rocks is strong evidence that this gold was not introduced with classic Carlin-type mineralization. Collectively, these features show that the Devonian strata were significantly enriched in gold some 300 m.y. prior to generation of the mid-Tertiary Carlin-type deposits. These strata may have been an important, perhaps even vital, source of gold for the latter. Although gold is typically low in most Zn-Pb-rich sedex deposits, our evidence suggests that transport of gold in basinal fluids, and its subsequent deposition in the sedex environment, can be significant.

Geology↗
USGS1999

Guatemala jadeitites and albitites were formed by deuterium-rich serpentinizing fluids deep within a subduction zone

Jadeitites and albitites from the Motagua Valley, Guatemala, are high-pressure–low-temperature metasomatic rocks that occur as tectonic inclusions in serpentinite-matrix melange. Metasomatism was driven by a fluid with a δ 18 O H2O value of 6‰, and a δD H2O value that is high in comparison with metamorphic fluids at other high-pressure–low-temperature localities of similar grade. We infer that the fluid was originally seawater that was entrained during subduction either as mineral-bound H 2 O or as free pore waters. The fluid drove serpentinization reactions in ultramafic rocks, possibly leading to deuterium enrichment of H 2 O, prior to forming the jadeitites and albitites at a depth of 29 ± 11 km. There are isotopic and fluid-inclusion similarities to rodingites, which are Ca-rich metasomatites found at other serpentinite localities. Our results suggest that the serpentinization process, whether it occurs within subduction zones or on the flanks of oceanic spreading ridges, may produce residual fluids that are H 2 O rich, have 1–8 wt% equivalent NaCl, and have high, perhaps seawater-like, δD values.

Geology↗
USGS1998

Accounting for cyanide and its degradation products at three Nevada gold mines; constraints from stable C- and N-isotopes

An understanding of the fate of cyanide (CN-) in mine process waters is important for addressing environmental concerns and for taking steps to minimize reagent costs. The utility of stable isotope methods in identifying cyanide loss pathways has been investigated in case studies at three Nevada gold mines. Freshly prepared barren solutions at the mines have cyanide d15N and d13C values averaging -4 ? and -36 ?, respectively, reflecting the nitrogen and carbon sources used by commercial manufacturers, air and natural gas methane. Pregnant solutions returning from ore heaps display small isotopic shifts to lower d15N and d13C values. The shifts are similar to those observed in laboratory experiments where cyanide was progressively precipitated as a cyanometallic compound, and are opposite in sign and much smaller in magnitude than the shifts observed in experiments where HCN was offgassed. Offgassing is inferred to be a minor cyanide loss mechanism in the heap leach operations at the three mines, and precipitation as cyanometallic compounds, and possibly coprecipitation with ferric oxides, is inferred to be an important loss mechanism. Isotopic analysis of dissolved inorganic carbon (DIC) shows that uptake of high d13C air CO2 has been important in many barren and pregnant solutions. However, DIC in reclaim pond waters at all three mines has low d13C values of -28 to -34 ? indicating cyanide breakdown either by hydrolysis or by other chemical pathways that break the C-N bond. Isotope mass balance calculations indicate that about 40 % of the DIC load in the ponds, at a minimum, was derived from cyanide breakdown. This level of cyanide hydrolysis accounts for 14-100 % of the dissolved inorganic nitrogen species present in the ponds. Overall, isotope data provide quantitative evidence that only minor amounts of cyanide are lost via offgassing and that significant amounts are destroyed via hydrolysis and related pathways. The data also highlight the possibility that significant cyanide may be either retained in the ore heaps or destroyed via other chemical pathways.

Open-File Report↗
USGS1997

Natural or fertilizer-derived uranium in irrigation drainage: A case study in southeastern Colorado, U.S.A.

Drainage from heavily cultivated soils may be contaminated with U that is leached from the soil or added as a trace constituent of PO4-based commercial fertilizer. The effect of decades-long application of U-rich fertilizer on the U concentration of irrigation drainage was investigated in a small (14.2 km2) drainage basin in southeastern Colorado. The basin was chosen because previous reports indicated locally anomalous concentrations of dissolved NO3(6-36 mg l-1) and dissolved U (61 ??g l-1) at the mouth of the only stream. Results of this study indicated minimal impact of fertilizer-U compared to natural U leached from the local soils. Detailed sampling of the stream along a 6 mile (9.7 km) reach through heavily cultivated lands indicated marked decoupling of the buildup of dissolved NO3 and U. Dissolved U increased markedly in the upstream half of the reach and correlated positively with increases in Na, Mg, SO4, B and Li derived from leaching of surrounding shaley soils. In contrast, major increases in dissolved NO3 occurred farther downstream where stream water was heavily impacted by ground water return from extensively fertilized fields. Nitrogen isotopic measurements confirmed that dissolved NO3 originated from fertilizer and soil organic N (crop waste). Uranium isotopic measurements of variably uraniferous waters showed little evidence of contamination with fertilizer-derived U of isotopically distinct 234U/238U alpha activity ratio (A.R. = 1.0). Leaching experiments using local alkaline soil, irrigation water and U-rich fertilizer confirmed the ready leachability of soil-bound U and the comparative immobility of U added with liquid fertilizer. Relatively insoluble precipitates containing Ca-P-U were formed by mixing liquid fertilizer with water containing abundant dissolved Ca. In the local soils soluble Ca is provided by dissolution of abundant gypsum. Similar studies are needed elsewhere because the mobility of fertilizer-derived U is dependent on fertilizer type, porewater chemistry and soil properties (pH, moisture, mineralogy, texture).

Applied Geochemistry↗
USGS1996

Cierco Pb-Zn-Ag vein deposits: Isotopic and fluid inclusion evidence for formation during the mesozoic extension in the pyrenees of Spain

The Cierco Pb-Zn-Ag vein deposits, located in the central Pyrenees of Spain, crosscut Paleozoic metasedimentary rocks and are in close proximity to Hercynian granodiorite dikes and plutons. Galena and sphalerite in the deposits have average delta 34 S values of - 4.3 and - 0.8 per mil (CDT), respectively. Coexisting mineral pairs give an isotopic equilibration temperature range of 89 degrees to 163 degrees C which overlaps with the 112 degrees to 198 degrees C range obtained from primary fluid inclusions. Coexisting quartz has a delta 18 O value of 19 + or - 1 per mil (VSMOW). The fluid which deposited these minerals is inferred to have had delta 18 O (sub H 2 ) O and delta 34 S (sub H 2 ) S values of 5 + or - 1 and -1 + or - 1 per mil, respectively. Chemical and microthermometric analyses of fluid inclusions in quartz and sphalerite indicate salinities of 3 to 29 wt percent NaCl equiv with Na (super +) and Ca (super 2+) as the dominant cations in solution. The Br/Cl and I/Cl ratios differ from those characteristic of magmatic waters and pristine seawater, but show some similarity to those observed in deep ground waters in crystalline terranes, basinal brines, and evaporated seawater. Barite, which postdates the sulfides, spans isotopic ranges of 13 to 21 per mil, 10 to 15 per mil, and 0.7109 to 0.7123 for delta 34 S, delta 18 O, and 87 Sr/ 86 Sr, respectively. The three parameters are correlated providing strong evidence that the barites are products of fluid mixing.We propose that the Cierco deposits formed along an extensional fault system at the margin of a marine basin during the breakup of Pangea at some time between the Early Triassic and Early Cretaceous. Sulfide deposition corresponded to an upwelling of hydrothermal fluid from the Paleozoic basement and was limited by the amount of metals carried by the fluid. Barite deposition corresponded to the waning of upward flow and the collapse of sulfate-rich surface waters onto the retreating hydrothermal plume. Calcite precipitated late in the paragenesis as meteoric or marine waters descended into the fault system, possibly during a regression in the overlying basin.There are other deposits resembling Cierco elsewhere in the Iberian peninsula. Taken as a group, they are evidence that hydrothermal circulation systems were widespread during Mesozoic extension. Differences among the deposits can be related to the fact that H 2 S and other solutes had local and variable sources.

Economic Geology↗
USGS1994

Partitioning of zinc among common ferromagnesian minerals and implications for hydrothermal mobilization

In systems where metals are scavenging from crystalline rocks by through-flowing fluids, the important host minerals must be dissolved or must undergo cation-exchange reactions with the fluid. Whereas copper resides in sulfides, zinc resides in magnetic and, to a lesser extent, in biotite, clinopyroxene and olivine. Magnetite is known from petrographic studies to be more resistant to alteration than sulfides. For metals extracted from crystalline rocks, the Cu:Zn mass ratio may thus decrease with progressive alteration. In systems where metals are scavenged from cooling magmas by exsolving fluids, the metals are partitioned among melt, fluid and any crystals that have fractionated. For zinc, crystal fractionation may be an important sink if magnetite or biotite crystallize before fluid saturation. The zinc concentrations of magmatic fluids will thus be reduced. -from Author

Canadian Mineralogist↗