Search USGS⌕ Search

Geology topics

J. T. Nash

Publications and source records attributed to J. T. Nash.

At least 37 records · Page 2Linked to original sources
USGS1987

Interpretation of the regional geochemistry of the Tonopah 1 degree by 2 degrees Quadrangle, Nevada, based on analytical results from stream-sediment and nonmagnetic heavy-mineral-concentrate samples

Results of more than 2,400 analyses of <0.25-mm fraction of stream sediments and nonmagnetic heavy-mineral concentrates from stream sediments from 1,217 sites in the Tonopah quadrangle demonstrate the existence of anomalous concentrations of many metals of economic interest in many areas. Single-element anomalies of As, Pb, or Sb in stream sediment provide general guides to possible mineralization, but multi-element suites are more reliable to characterize types of mineralization. Various combinations of Ag, As, Bi, Cu, Mo, Pb, Sb, and W in stream sediments and concentrates provide guides to five general types of deposits and their geologic environments. Multi-element suites that recur in stream-sediment media resemble those observed in mineralized rock samples, and the distribution of the suites corresponds to the distribution of known types of deposits and to the general geology of the region. Multi-element geochemical anomalies are prominent in the Pilot Mountains, Monte Cristo Range, Paradise Range, Lone Mountain, northeastern Toiyabe Range, Cedar Mountains, and Toquima Range. Strongest multi-element anomalies are associated with plutonic rocks in the western part of the quadrangle. Two base-metal suites are enriched in and around plutons: (1) Bi + W + Pb + Mo ± As, Cu, Sb, a suite that resembles metals enriched in rocks samples from skarn deposits; and (2) Pb + Mo ± As,Cu,Sb, which resembles base-metal enrichments in sulfide vein and replacement deposits, generally associated with intrusions. A third variety of base-metal enrichment that contains Ag is distinguished for its possible economic importance. This Ag-Pb-rich suite occurs both near plutons and in volcanic terrane and generally is near areas of known Ag-rich polymetallic deposits. Many sites are characterized by modest enrichments of two to five elements in the suite As-Mo-Sb-Zn-Ag that resemble enrichments in epithermal ore deposits. Many anomalies of this type are from drainages underlain by Tertiary welded tuff, commonly lacking alteration and mineral prospects. Some of these anomalous sites correlate with areas of known epithermal deposits or siliceous alteration of calcareous rocks, thus this suite may be a guide to precious-metal deposits if there is supporting geologic evidence. The results from regional sampling of stream sediments, utilizing the <0.25-mm fraction and nonmagnetic heavy-mineral-concentrate media, effectively outline most areas of known deposits or alteration in the Tonopah quadrangle. Some clusters of anomalies are larger than the area of known mineral prospects, suggesting that other deposits remain to be discovered. This regional geochemical information is most effective for exploration and resource analysis when integrated with other geologic information, especially rock alteration.

Nevada↗
USGS1986

Geochemistry of altered and mineralized rocks from the Morey and Fandango Wilderness Study Areas, northern Hot Creek Range, Nye County, Nevada

The U.S. Geological Survey and the St. Johns River Water Management District are investigating the hydrogeology of the Floridan aquifer system. An essential element of this investigation is the design and construction of a monitor well network in the lower saline water-bearing zone which occurs at about 2,000 ft below land surface. During 1985, a well near Ponte Vedra in northeast St. Johns County was completed into the lower saline water-bearing zone at a depth of 1,980 to 2,035 ft below land surface. This well and other wells drilled under this or other programs will be used to monitor water levels and water chemistry of the lower saline zone. Chloride concentrations in water above the lower saline zone ranged from 14 to 270 mg/L and specific conductance ranged from 450 to 1,440 micromhos/cm c. In the lower zone, chloride concentrations were as much as 16,210 mg/L and specific conductance as much as 46,000 micromhos per centimeter. Aquifer head and artesian flow from the well generally increased with depth. Water temperatures also increased from 23 C in the upper part of the aquifer to more than 28 C in the lower saline zone. (USGS)

Open-File Report↗
USGS1982

Progress report on geologic studies of the Ranger orebodies, Northern Territory, Australia

The Ranger No. 1 and No. 3 orebodies contain about 124,000 tonnes U3O8 in highly chloritized metasediments of the lower Proterozoic Cahill Formation within about 500 m of the projected sub-Kombolgie Formation unconformity. In both orebodies, oxidized and reduced uranium minerals occur chiefly in quartzose schists that have highly variable amounts of muscovite, sericite, and chlorite. The effects of several periods of alteration are pervasive in the vicinity of orebodies where biotite and garnet are altered to chlorite, and feldspars to white mica or chlorite. Oxidized uranium minerals, associated with earthy iron oxides, occur from the surface to a depth of about 60 m. Below the oxidized zone, uranium occurs chiefly as uraninite and pitchblende disseminated through thick sections of quartz-chlorite-muscovite schist and has no apparent association with graphite or sulfides. In fact, graphite is rare and sulfides are generally low in abundance (<0.5 percent). Higher ore grades occur in disrupted zones a few centimeters thick and in some quartz-chlorite vein-like zones of uncertain origin. Uranium correlates strongly with chlorite, but not all of the many ages of chlorite have associated uranium. At least five textural varieties of chlorite are present and represent at least 3 ages. Preliminary microprobe analyses suggest that Mg-Fe-Al contents are relatively uniform. Apatite commonly occurs with chlorite. Uranium is not common in carbonate rocks and seems to occur only in disrupted zones that have chlorite alteration. Chloritization and silicification are more widespread and intense in the No. 1 orebody than in the No. 3. In both orebodies, hematite occurs tens to hundreds of meters below the weathered zone, in both altered and largely unaltered rocks, with and without uranium. The structure of the orebodies is outwardly simple, particularly in No. 3; dips are less than 40? on most lithologic contacts. The No. 1 orebody is in a basin-like structure about 400 m wide that probably formed in part by progressive removal of carbonate rocks that are as much as 200 m thick adjacent to the No. 1 orebody and below the No. 3 orebody. Quartz-chlorite breccias have formed in the zone of carbonate thinning; uranium is spotty and low grade in these breccias. Chloritized and uraniferous broken and sheared zones, a few centimeters to a few meters thick, have an unknown attitude but must have small displacement. Blocks of altered Kombolgie sandstone are downfaulted into the No. 3 orebody and locally contain reduced uranium minerals. One or more shear zones 5-30 m thick of crushed and smeared fine to coarse rock fragments occur below the orebodies, and other low-angle shears probably occur in the orebodies. The shear zone dips about 40 o and displacement on it is not known. The footwall rocks generally are less retrograded than those in the hanging wall (orebody) and consist of quartz-biotite-feldspar schists and gneisses flanking the Nanambu Complex. A few scattered fractures in the footwall sequence contain pitchblende of unknown age and origin. Major element chemical analyses confirm the lithologic observations of large changes in composition during multiple stages of alteration. Granitic dikes and pelitic schists have gained Fe and Mg and lost Si, Ca, Na, and K during chloritization. Marbles have gained Si, Al, Fe, and P, and lost Mg, Ca, and K during jasperoid-chlorite alteration. Total net chemical gains and losses in the Ranger No. 1 orebody were huge: equal to about 37 percent of the mass of the ore-bearing rock that will be mined. There were net gains in Si and P and net losses in Al, Fe, Mg, Ca, K, and Na. The geologic age(s) of uranium emplacement are obscure because there are few age criteria. Reduced uranium minerals are younger than 1.8-b.y.-old granite dikes, and some occur locally in 1.65-b.y.-old Kombolgie Formation. Diabase dikes (age not known) are thoroughly chloritized and contain sparse ore minerals. Oxidized ura

Open-File Report↗
USGS1981

U-Pb isotope systematics and age of uranium mineralization, Midnite mine, Washington.

Uranium ores at the Midnite mine, near Spokane, Washington, occur in phyllites and calcsilicates of the Proterozoic Togo Formation, near the margins of an anomalously uraniferous, porphyritic quartz monzonite of Late Cretaceous age. The present geometry of the ore zones is tabular, with the thickest zones above depressions in the pluton-country rock contact. Analyses of high-grade ores from the mine define a 207 Pb/ 204 Pb- 235 U/ 204 Pb isochron indicating an age of mineralization of 51.0 + or - 0.5 m.y. This age coincides with a time of regional volcanic activity (Sanpoil Volcanics), shallow intrusive activity, erosion, and faulting. U-Th-Pb isotopic ages of zircons from the porphyritic quartz monzonite in the mine indicate an age of about 75 m.y., hence the present orebodies were formed about 24 m.y. after its intrusion. The 51-m.y. time of mineralization probably represents a period of mobilization and redeposition of uranium by supergene ground waters, perhaps aided by mild heating and ground preparation and preserved by a capping of newly accumulated, impermeable volcanic rocks. It seems most likely that the initial concentration of uranium occurred about 75 m.y. ago, probably from relatively mild hydrothermal fluids in the contact-metamorphic aureole of the U-rich porphyritic quartz monzonite.Pitchblende, coffinitc, pyrite, marcasite, and hisingerite are the most common minerals in the uranium-bearing veinlets, with minor sphalerite and chalcopyrite. Coffinitc with associated marcasite is paragenetically later than pitchblende, though textural and isotopic evidence suggests no large difference in the times of pitchblende and colfinite formation.The U-Pb isotope systematics of total ores and of pitchblende-coffinite and pyrite-marcasite separates show that whereas open system behavior for U and Pb is essentially negligible for large (200-500 g) ore samples, Pb migration has occurred on a scale of 1 to 10 mm (out of pitchblende and coffinite and into pyrite and marcasite). Also, long-term continuous leakage of radioactive daughters of 238 U (probably 222 Rn) has occurred on scales of from approximately 100 mu m approximately 10 cm. The isotopic composition of unsupported radiogenic Pb in pyrite-marcasite seems to depend on the mineralogical microenvironment of the grains, so that the radiogenic Pb in pyrite-marcasite intimately intermixed with pitchblende-coffinite tends to be deficient in 206 Pb, and the radiogenic Pb in pyrite-marcasite in gangue tends to have excess 206 Pb. These systematics probably reflect differences between the average distances of Pb and 222 Rn diffusion since the formation of the ores.

Washington↗