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J. M. Motooka

Publications and source records attributed to J. M. Motooka.

At least 55 records · Page 3Linked to original sources

Map showing distribution of gold in stream-sediment samples, Richfield 1° x 2° quadrangle, Utah

This map of the Richfield 1° x 2° quadrangle, Utah, shows the regional distribution of gold in the less-than-0.180-mm (minus-80-mesh) fraction of stream sediments. It is part of a folio of maps of the Richfield 1° x 2° quadrangle, Utah, prepared under the Conterminuous United States Mineral Assessment Program. Other published geochemical maps in this folio are listed in the Selected References of this report. The Richfield quadrangle is located in west-central Utah and includes the eastern part of the Pioche-Marysvale igneous and mineral belt, which extends from the vicinity of Pioche in southeastern Nevada, east-northeastward for 155 miles into central Utah. The western two-thirds of the Richfield quadrangle is part of the Basin and Range province, whereas the eastern third is part of the High Plateaus of Utah, a subprovince of the Colorado Plateau. Bedrock in the northern part of the Richfield quadrangle consists predominantly of Late Proterozoic and Paleozoic sedimentary strata that were thrust eastward during the Sevier orogeny in Cretaceous time onto an autochthon of Mesozoic sedimentary rocks located in the eastern part of the quadrangle. The southern part of the quadrangle is largely underlain by Oligocene and younger volcanic rocks and related intrusions. Extensional tectonism in late Cenozoic time broke the bedrock terrain into a series of north-trending fault blocks; the uplifted mountain areas were eroded to various degrees and the resulting debris was deposited in adjacent basins. Most of the mineral deposits in the Pioche-Marysvale mineral belt were formed as a result of igneous activity in the middle and late Cenozoic time. A more complete description of the geology and a mineral-resource appraisal of the Richfield quadrangle appears in Steven and Morris (1984 and 1987). The regional sampling program was designed to define broad geochemical patterns and trends that can be utilized along with geological and geophysical data to assess the mineral-resource potential for this quadrangle. Reconnaissance geochemical surveys are valuable tools in mineral exploration, especially when used in conjunction with data obtained from other earth science disciplines. Identifying specific exploration targets generally involves additional, more detailed investigations.

Utah

An exploration geochemical technique for the determination of preconcentrated organometallic halides by ICP-AES

An atomic absorption extraction technique which is widely used in geochemical exploration for the determination of Ag, As, Au, Bi, Cd, Cu, Mo, Pb, Sb, and Zn has been modified and adapted to a simultaneous inductively coupled plasma-atomic emission instrument. The experimental and operating parameters are described for the preconcentration of the metals into their organometallic halides and for the determination of these metals. Lower limits of determination are equal to or improved over those for flame atomic absorption (except Au), and ICP results are very similar to the accepted AA values, with precision for the ICP data in excess of that necessary for exploration purposes.

Applied Spectroscopy

Mineralogical basis for the interpretation of multi-element (ICP-AES), oxalic acid, and aqua regia partial digestions of stream sediments for reconnaissance exploration geochemistry

We have applied partial digestion procedures, primarily oxalic acid and aqua regia leaches, to several regional geochemical reconnaissance studies carried out using Inductively Coupled Plasma-Atomic Emission Spectroscopy (ICP-AES) analytical methods. We have chosen to use these two acids because the oxalic acid primarily attacks those compounds formed during secondary geochemical processes, whereas aqua regia will digest the primary sulfide phases as well as secondary phases. Application of the partial digestion technique has proven superior to total digestion because the concentration of metals in hydromorphic compounds and the sulfides is enhanced relative to the metals bound in the unattacked silicate phases. The aqua regia digestion attacks and leaches metals from the mafic chain silicates and the phyllosilicates (coordination number of VI or more), yielding a characteristic geochemical signature, but does not leach appreciable metal from many other silicates. In order to interpret the results from these leach studies, we have initiated an investigation of a large suite of hand-picked mineral separates. The study includes analyses of about two hundred minerals representing the common rock-forming minerals as well as end-member compositions of various silicates, oxides, sulfides, carbonates, sulfates, and some vanadates, molybdates, tungstates, and phosphates. The objective of this study is to evaluate the effect of leaching by acids of particular lattice sites in specific mineral structures.

Journal of Geochemical Exploration