Age and paleoclimatic significance of the Stansbury shoreline of Lake Bonneville, Northeastern Great Basin     

Charles G. Oviatt  Donald R. Currey  David M. Miller 《Quaternary Research》1990,33(3)

The Stansbury shoreline, one of the conspicuous late Pleistocene shorelines of Lake Bonneville, consists of tufa-cemented gravel and barrier beaches within a vertical zone of about 45 m, the lower limit of which is 70 m above the modern average level of Great Salt Lake. Stratigraphic evidence at a number of localities, including new evidence from Crater Island on the west side of the Great Salt Lake Desert, shows that the Stansbury shoreline formed during the transgressive phase of late Pleistocene Lake bonneville (sometime between about 22,000 and 20,000 yr B.P.). Tufa-cemented gravel and barrier beaches were deposited in the Stansbury shorezone during one or more fluctuations in water level with a maximum total amplitude of 45 m. We refer to the fluctuations as the Stansbury oscillation. The Stansbury oscillation cannot have been caused by basin-hypsometric factors, such as stabilization of lake level at an external overflow threshold or by expansion into an interior subbasin, or by changes in drainage basin size. Therefore, changes in climate must have caused the lake level to reverse its general rise, to drop about 45 m in altitude (reducing its surface area by about 18%, 5000 km²), and later to resume its rise. If the sizes of Great Basin lakes are controlled by the mean position of storm tracks and the jetstream, which as recently postulated may be controlled by the size of the continental ice sheets, the Stansbury oscillation may have been caused by a shift in the jetstream during a major interstade of the Laurentide ice sheet.  相似文献   

Pahoehoe and aa in Hawaii: volumetric flow rate controls the lava structure     

Scott K Rowland  George PL Walker 《Bulletin of Volcanology》1990,52(8):615-628

The historical records of Kilauea and Mauna Loa volcanoes reveal that the rough-surfaced variety of basalt lava called aa forms when lava flows at a high volumetric rate (>5–10 m³/s), and the smooth-surfaced variety called pahoehoe forms at a low volumetric rate (<5–10 m³/s). This relationship is well illustrated by the 1983–1990 and 1969–1974 eruptions of Kilauea and the recent eruptions of Mauna Loa. It is also illustrated by the eruptions that produced the remarkable paired flows of Mauna Loa, in which aa formed during an initial short period of high discharge rate (associated with high fountaining) and was followed by the eruption of pahoehoe over a sustained period at a low discharge rate (with little or no fountaining). The finest examples of paired lava flows are those of 1859 and 1880–1881. We attribute aa formation to rapid and concentrated flow in open channels. There, rapid heat loss causes an increase in viscosity to a threshold value (that varies depending on the actual flow velocity) at which, when surface crust is torn by differential flow, the underlying lava is unable to move sufficiently fast to heal the tear. We attribute pahoehoe formation to the flowage of lava at a low volumetric rate, commonly in tubes that minimize heat loss. Flow units of pahoehoe are small (usually <1 m thick), move slowly, develop a chilled skin, and become virtually static before the viscosity has risen, to the threshold value. We infer that the high-discharge-rate eruptions that generate aa flows result from the rapid emptying of major or subsidiary magma chambers. Rapid near-surface vesiculation of gas-rich magma leads to eruptions with high discharge rates, high lava fountains, and fast-moving channelized flows. We also infer that long periods of sustained flow at a low discharge rate, which favor pahoehoe, result from the development of a free and unimpeded pathway from the deep plumbing system of the volcano and the separation of gases from the magma before eruption. Achievement of this condition requires one or more episodes of rapid magma excursion through the rift zone to establish a stable magma pathway.  相似文献   

Erratum     

F. David  L. Walker 《Contributions to Mineralogy and Petrology》1991,107(1):135-135

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Estimating Geohydrologic Properties from Borehole-Geophysical Logs     

Donald G. Jorgensen 《Ground Water Monitoring & Remediation》1991,11(3):123-129

Borehole-geophysical logs can be used to estimate geohydrologic properties based on in situ measurement of rock and water properties. Estimates of properties of both formation and water, such as coefficient of diffusion, formation factor, cementation exponent, hydraulic conductivity, irreducible water content and specific yield can be assessed from borehole-geophysical data and selected algorithms and graphs.
Water properties, such as resistivity, sodium chloride concentration, viscosity and density, can also be estimated using data from borehole-geophysical logs. Water resistivity using the spontaneous-potential method can be estimated if an empirical correction for fresh water is applied.
Estimates of formation properties, such as porosity and permeability, can also be made using borehole-geophysical data.  相似文献   

Partitioning of siderophile elements in the FeNiS system: 1 bar to 80 kbar     

J.H. Jones  D. Walker 《Earth and Planetary Science Letters》1991,105(1-3)

Partition coefficients for Au, Ni, P and Ge between solid FeNi metal and sulfur-bearing metallic liquids have been measured at 7,27 and 80 kbar. To our knowledge, these are the only such data for Au, P and Ge at high pressure. Comparison of our partitioning results to those obtained at 1 bar indicate that only the 80 kbar Ge data differ significantly from the 1-bar experiments. Thus, many low-pressure partitioning experiments in the FeNiSP system may have applicability to the greater portion of the Earth's upper mantle or, alternatively, the entire mantle of Mars.  相似文献   

THE NEW DECADE: DIGITS AND DIVERSITY     

I. Newton  J. D. Leatherdale    J.-P. Muller  M. Sowton  A. S. Walker 《The Photogrammetric Record》1991,13(78):877-888

The President of the Photogrammetric Society, Mr. I Newton, chaired a panel discussion concerned with those developments in photogrammetry which may take place during the 1990s.  相似文献   

Genesis and solvus relations of submicroscopically intergrown paragonite and phengite in a blueschist from northern California     

Yen-Hong Shau  Melanie E. Feather  Eric J. Essene  Donald R. Peacor 《Contributions to Mineralogy and Petrology》1991,106(3):367-378

Electron microbeam techniques have been used to examine submicroscopically intergrown paragonite, phengite and chlorite from the South Fork Mountain Schist of the Franciscan Terrane of northern California, which was subjected to blueschist facies metamorphism. The sample also contains quartz, albite, lawsonite, and rutile. The subassemblage albite-lawsonite-rutile requires metamorphic conditions on the low-temperature side of the equilibrium albite+lawsonite+rutile=paragonite+sphene+quartz+H₂O (T<200° C and P<7.4 kbars based on thermodynamic data of Holland and Powell 1990). The white micas appear to be optically homogeneous, but back-scattered electron images can distinguish two different micas by their slight difference in contrast. Electron microprobe analyses (EMPA) of micas show Na/(Na+K) ranging from 0.2 to 0.8. The two micas are resolved by transmission electron microscopy (TEM) as packets of phengite and paragonite that range from 20 to several hundred nm in thickness. The compositions, determined by analytical electron microscopy (AEM), constrain the limbs of the phengite-paragonite solvus to values of Na/(Na+K)=<0.02 and 0.97, representing less mutual solid solution than ever reported by EMPA. The textural relations imply that the sheet silicates were derived from reactions between fluids and detrital clays and that they are in an intermediate stage of textural development. We caution that microprobe analyses of apparently homogeneous sheet silicates may yield erroneous data and lead to faulty conclusions using phengite barometry and paragonite-muscovite thermometry, especially in fine-grained rocks that formed at relatively low temperatures. Contribution no. 473 from the Mineralogical Laboratory, Department of Geological Sciences, The University of Michigan, Ann Arbor, Michigan, USA  相似文献   

The Batu Hijau porphyry copper-gold deposit, Sumbawa Island, Indonesia   总被引：4，自引：0，他引：4  

Simon J. Meldrum  Romeo S. Aquino  Rene I. Gonzales  Robert J. Burke  Artha Suyadi  Bambang Irianto  Donald S. Clarke 《Journal of Geochemical Exploration》1994,50(1-3)

The Batu Hijau porphyry Cu---Au deposit lies in southwest Sumbawa Island, Indonesia. It is a world-class porphyry Cu deposit in an island are setting, and is typical of this deposit type in most features, including igneous association, morphology, hydrothermal alteration and mineralisation style.The region was not previously recognised as a porphyry Cu province; disseminated Cu sulphides were first recognised in float samples in southwest Sumbawa in 1987. Associated stream sediment sampling identified a broad area of anomalous Au and Cu in an area of greater than 5 km² around Batu Hijau, including 169 ppb Au in BLEG samples and 580 ppm Cu in stream silts 1 km from the deposit. Mineralisation in bedrock at surface contains > 0.1 wt % Cu and > 0.1 ppm Au over an area of 0.6 km × 1.2 km, including a zone 300 m × 900 m containing > 0.3 wt % Cu. Areas with elevated Mo (> 30 ppm) form a distinctive annulus around this Cu-rich zone.Batu Hijau mineralisation is hosted in a tonalite intrusive complex, and diorite and metavolcanic wallrocks. There are no post-mineralisation igneous intrusions or breccia pipes within the deposit. The main tonalite intrusion forms a stock in the centre of the deposit, where it generally displays intensely pervasive potassic (biotite with magnetite-quartz) alteration and hosts most of the higher grade mineralisation. Younger tonalite dykes intruding the centre of this stock are generally less altered and mineralised than the older tonalite.The core zone of potassic alteration grades outward into extensive propylitic alteration (chlorite-epidote), with both variably overprinted by widespread fracture controlled intermediate argillic alteration (sericite-chlorite), and minor phyllic (sericite-pyrite) and sodic (albite) alteration. Argillic (sericite-kaolinite) and advanced argillic (kaolinite-alunite-pyrophyllite) assemblages occur near surface.Copper and Au grades within the orebody show a positive correlation with quartz stockwork intensity, although disseminated Cu sulphides are also common. Chalcopyrite and bornite are the principle hypogenal minerals, with minor chalcocite. Oxidation extends to a depth of 5 m to 85 m below surface across the deposit, and is underlain by weak supergene mineralisation. Drill testing of the deposit down to 650 m below surface reveals a single cylindrical to conical orebody of 334 million tonnes grading 0.8 wt % Cu and 0.69 gm per tonne Au; the depth extent of mineralisation is unknown.  相似文献   

PHOTOGRAMMETRIC SOCIETY COUNCIL ACTIVITIES     

S. Walker 《The Photogrammetric Record》1985,11(66):755-758

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The geochemistry of Ca,Sr, Ba and Ra sulfates in some deep brines from the Palo Duro Basin,Texas     

Donald Langmuir  Daniel Melchior 《Geochimica et cosmochimica acta》1985,49(11):2423-2432

The geochemistry of Ca, Sr, Ba and Ra sulfates in some deep brines from the Palo Duro Basin of north Texas, was studied to define geochemical controls on radionuclides such as ⁹⁰Sr and ²²⁶Ra. Published solubility data for gypsum, anhydrite, celestite, barite and RaSO₄ were first reevaluated, in most cases using the ion interaction approach of Pitzer, to determine solubility products of the sulfates as a function of temperature and pressure. Ionic strengths of the brines were from 2.9 to 4.8 m, their temperatures and pressures up to 40°C and 130 bars. Saturation indices of the sulfates were computed with the ion-interaction approach in one brine from the arkosic granite wash fades and four from the carbonate Wolfcamp Formation. All five brines are saturated with respect to gypsum, anhydrite and celestite, and three of the five with respect to barite. All are undersaturated by from 5 to 6 orders of magnitude with respect to pure RaSO₄. ²²⁶Ra concentrations in the brines, which ranged from 10^?11.3 to 10^?12.7 m, are not controlled by RaSO₄ solubility or adsorption, but possibly by the solubility of trace Ra solid solutions in sulfates including celestite and barite.  相似文献