Geology topics

E. Dewitt

Publications and source records attributed to E. Dewitt.

4 recordsLinked to original sources

USGS2001

Major brazilian gold deposits - 1982 to 1999

Brazil has been a major but intermittent producer of gold since its discovery in 1500. Brazil led the world in gold production during the 18th and early 19th centuries. From the late 19th century to the late 20th century, total mining company and garimpeiro production was small and relatively constant at about 5 to 8 t/year. The discovery of alluvial deposits in the Amazon by garimpeiros in the 1970s and the opening of eight mines by mining companies from 1983 to 1990 fueled a major boom in Brazil's gold production, exceeding 100 t/year in 1988 and 1989. However, garimpeiro alluvial production decreased 'rapidly in the 1990s, to about 10 t/year by 1999. Company production increased about tenfold from about 4 t/year in 1982 to 40 t in 1992. Production from 1992 to the present remained relatively stable, even though several mines were closed or were in the process of closing and no new major mines were put into production during that period. Based on their production history from 1982-1999, 17 gold mines are ranked as major (> 20 t) and minor (3-8 t) mines. From 1982-1999, deposits hosted in Archean rocks produced 66% of the gold in Brazil, whereas deposits in Paleoproterozoic and Neoproterozoic rocks accounted for 19% and 15%, respectively. Deposits in metamorphosed sedimentary rocks, especially carbonate-rich rocks and carbonate iron-formation, yielded the great bulk of the gold. Deposits in igneous rocks were of much less importance. The Archean and Paleoproterozoic terranes of Brazil largely lack base-metal-rich volcanogenic massive sulfide deposits, porphyry deposits, and polymetallic veins and sedimentary exhalative deposits. An exception to this is in the Caraja??s Mineral Province.

Mineralium Deposita↗

USGS2001

Evidence and characteristics of hydrolytic disproportionation of organic matter during metasomatic processes

Petroleum-geochemical analyses of carbonaceous regionally metamorphosed rocks, carbonaceous rocks from ore deposits, and alkalic plutonic rocks from diverse settings, demonstrated the presence of very low to moderately low concentrations of solvent-extractable organic matter, this observation in spite of the fact that some of these rocks were exposed to extremely high metamorphic temperatures. Biomarker and ??13C analyses established that the extractable organic matter originated as sedimentary-derived hydrocarbons. However, the chemistry of the extractable bitumen has been fundamentally transformed from that found in sediment bitumen and oils. Asphaltenes and resins, as defined in the normal petroleum-geochemical sense, are completely missing. The principal aromatic hydrocarbons present in oils and sediment bitumens (especially the methylated naphthalenes) are either in highly reduced concentrations or are missing altogether, Instead, aromatic hydrocarbons typical of sediment bitumens and oils are very minor, and a number of unidentified compounds and oxygen-bearing compounds are dominant. Relatively high concentrations of alkylated benzenes are typical. The polar "resin" fraction, eluted during column chromatography, is the principal compound group, by weight, being composed of six to eight dominant peaks present in all samples, despite the great geologic diversity of the samples. These, and other, observations suggest that a strong drive towards equilibrium exists in the "bitumen." Gas chromatograms of the saturated hydrocarbons commonly have a pronounced hump in both the n-paraffins and naphthenes, centered near the C19 to C26 carbon numbers, and a ubiquitos minimum in the n-paraffin distribution near n-C12 to n-C14. Multiple considerations dictate that the bitumen in the samples is indigenous and did not originate from either surficial field contamination or from laboratory procedures. Our observations are consistent with the hydrolytic disproportion of organic matter (HDOM), in which water and organic matter, including hydrocarbons, easily exchange hydrogen or oxygen with one another under certain conditions (Helgeson et al., 1993). The process appears to take place via well-known organic-chemical redox reaction pathways and is most evident in open-fluid systems. The conclusion that HDOM took place in the analyzed samples, thus producing the chemistry of the extractable bitumen, is supported by numerous previously published organic-geochemical studies of metamorphic, volcanic, plutonic, and ore-deposit-related rocks by other investigators. HDOM is suggested as an unrecognized geologic agent of fundamental importance. The process appears to control major chemical reactions in diverse geologic environments including, but not limited to, petroleum geology and geochemistry, regional metamorphism, and base- and precious-metal ore deposition. Copyright ?? 2001 Elsevier Science Ltd.

Geochimica et Cosmochimica Acta↗

USGS1993

The Mount Evans batholith in the Colorado Front Range: Revision of its age and reinterpretation of its structure

The Mount Evans batholith, in the central Front Range of Colorado, is composed of a main phase of massive to conspicuously foliated monzogranite and granodiorite and undeformed aplite and pegmatite. The Mount Evans batholith was previously considered to be part of the 1.7 Ga Routt Plutonic Suite. New U-Pb zircon ages on four samples (granodiorite, monzogranite, and granite), however, indicate that the batholith was emplaced at 1,442 ± 2 Ma and belongs to the Berthoud Plutonic Suite. Most of the batholith has igneous textures and structures, except in the vicinity of the Idaho Springs-Ralston shear zone where those features are tectonically recrystallized and foliated. Foliation elsewhere in the batholith is a flow structure. Zircons in two granodiorite samples, collected near the shear zone (just south of the Colorado Mineral Belt), are reversely discordant by about 0.8%-2.1%, with a considerable spread in 207 Pb/ 206 Pb ages. Many of the zircons from these samples contain apatite, K-feldspar, and quartz inclusions that appear to replace zircon along cracks and imperfections from rim to core. We suggest that these inclusions formed during a Laramide ore-forming event and incorporated Early and Middle Proterozoic radiogenic lead scavenged from the country rock. The excess radiogenic lead caused the scatter and reverse discordance in the data. The Mount Evans batholith is anomalous in composition and structure compared to most other 1.4 Ga plutons of the southwestern United States. The differences probably reflect different sources of partial melting; the specific tectonic setting where rocks of such disparate origin are temporally and spatially juxtaposed is not understood.

Colorado↗

USGS1986

Late Cretaceous stratigraphy, deformation and intrusion in the Madison Range of southwestern Montana ( USA).

Dating of orogenic rock units in the central part of the Madison Range shows that Laramide deformation was virtually completed by the end of the Cretaceous. Early Campanian K-Ar dates of about 79 m.y. were obtained from welded tuffs in the basal part of the Livingston Formation, a volcanic and volcaniclastic assemblage that is conformable with underlying Cretaceous clastic rocks and with the overlying Sphinx Conglomerate. The Sphinx and the Livingston were deformed by the Hilgard fault system which extends along the western side of the southern two-thirds of the range. This north-trending fault system represents the culmination of Laramide shortening within the range. Dating of hornblende indicates an approximate date of 68-69 m.y. B.P. for emplacement of the igneous suite. The dacite postdates movement along faults of the Hilgard fault system, and postdates the synorogenic Sphinx Conglomerate. -from Authors

Geological Society of America Bulletin↗