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C. A. Johnson

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

24 records · Page 2Linked to original sources
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↗
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↗