UPb zircon and rutile chronology of Archean greenstone formation and gold mineralization in the Val d'Or region, Quebec

UPb geochronology provides an absolute time framework for the evolution of the Sigma gold deposit and surrounding rocks at Val d'Or, southern Abitibi subprovince. The Bourlamaque batholith, the largest pluton in the area, gives a 2699.8 ± 1.0 Ma UPb zircon age. This pluton cuts the Val d'Or Formation which hosts the mineralization. A UPb zircon age of 2704.9 ± 1.1 Ma on a felsic volcanic rock, the Colombière “rhyolite”, 13 km east of the mine dates that formation. The gold-bearing quartz vein system at Sigma is hosted by andesites and two generations of porphyry intrusions, all metamorphosed to the greenschist facies. The oldest porphyry (“porphyritic diorite”) shows the same deformation as the volcanic rocks, and has a 2703.7 ± 2.5 Ma UPb zircon age. The porphyritic diorite and volcanic rocks are cut by feldspar-porphyry dykes which post-date regional folding and have a 2694.0 ± 2.2 Ma UPb zircon age.Regional greenschist metamorphism has been dated directly, with a UPb date of 2684 ± 7 Ma on rutile in the Colombière “rhyolite”. The mineralization and hydrothermal alteration in the mine are superimposed on the metamorphic minerals. Hydrothermal rutile, from an alteration halo around the veins in andesite, has a 2599 ± 9 Ma UPb age. Textural evidence clearly indicates that the wall-rock alteration and vein filling are contemporaneous, and hence the vein system and gold mineralization appear to have developed at least 80 m.y. after the formation and metamorphism of host greenstones.     

Detecting Changes in Ground Water Quality at Regulated Facilities

The Resource Conservation and Recovery Act (PL 94–580) and related federal and state legislation have mandated routine monitoring of ground water quality at regulated facilities. The objective of the required monitoring activities is detection of adverse changes in ground water quality caused by the facilities.
Both failure to detect pollution and an incorrect determination of pollution can be very expensive. It is crucial, therefore, that monitoring programs be designed and operated to provide statistically sound information. It is equally important that users of ground water quality data understand the nature and limitations of information from monitoring.
To address the preceding issues, the authors present a general approach to analyzing ground water quality data in light of the stated monitoring objective. The suggested approach accounts for "natural" variation in background water quality through pairing of observations. The limitations of quarterly sampling for detecting small changes in quality over a short time frame are discussed.     

Aragonite dissolution on the Bermuda pedestal: Its depth and geochemical significance

The depth distribution of pteropod and planktonic foram tests, and fine-grained (<62 μm) aragonite, high-Mg calcite (12 mode mol.% MgCO₃), and low-Mg calcite has been determined for surface sediments of an area of the eastern slope of the Bermuda pedestal. Over the range 1800–3000 m, fine-grained aragonite and fine-grained high-Mg calcite gradually disappear relative to fine-grained low-Mg calcite, and pteropods gradually disappear relative to planktonic forams. This is interpreted as preferential dissolution of aragonite (and high-Mg calcite) relative to low-Mg calcite over this depth range. Coarse aragonitic debris derived from shallow-water organisms living on the Bermuda platform does not show consistent disappearance over the same depth zone. Chemical analyses of bottom water samples taken at the same time as some of the sediment samples indicate that the degree of saturation with respect to aragonite Ω_A over the zone of aragonite disappearance ranges from 0.55 to 0.85; i.e. major dissolution occurs only at Ω_A values distinctly less than one. These results lend credence to the hypothesis that CaCO₃ dissolution in the oceans, both as aragonite and as calcite, takes place mainly as a response to complex chemical kinetic phenomena and not as a result of the simple attainment of undersaturation (thermodynamic hypothesis) or the resuspension of bottom sediment (hydrodynamic hypothesis).     

Aspects of the cycle of inorganic nitrogen compounds in the tropical rain forest of the Ivory Coast

A partial balance of mineral N is given for the basins of two coastal rivers in a forest zone in the Ivory Coast. The dry and wet depositions on the basin surfaces is given for particulate matter (NO₃ ^–, NH₄ ⁺). The quantity of mineral N washed away in the rivers is evaluated. The losses from leaching of the soils by rainwater are about 0.33 to 1.0% of the atmospheric depositions for NH₄ ⁺–N and 2.2 to 5.8% for NO₃ ^––N. The yearly atmospheric input of N compounds to the ecosystem, about 1.4 g N m^–2 y^–1, is at least 14% of mineral N formed in the soils and is therefore quite significant.     

Relationship of atmospheric ozone profiles to solar magnetic activity

The observed relationship between atmospheric vorticity variations and solar magnetic sector boundary passages is examined for a possible connection via ionization changes affecting ozone distributions. A superposed epoch analysis was performed on Umkehr distributions for 18 years from Arosa, Switzerland, with use of more than 500 solar sector boundary passages as keyday zero. No significant responses are observed in any Umkehr level or in total observed ozone amounts. Further analyses on shorter records for Belsk, Poland, and Hohenpeissenberg, West Germany, corroborate these results. Another analysis for Arosa with about 100 type IV solar flares as keyday zero also shows no definitive trend. It is concluded that ozone distribution changes cannot be the primary causative mechanism for vorticity variations.Journal Paper No. J-8838 of the Iowa Agriculture and Home Economics Experiment Station, Ames, Iowa. Project No. 1852.     

Petrology and genetic significance of an ultramafic xenolith suite from Tahiti

A suite of ultramafic xenoliths 2–10 cm in size occurs in basanite near Papeete, Tahiti, and consists of spinel lherzolites with minor dunites and wehrlites. Petrographic examination of xenoliths reveals that they are typically coarse grained with well-developed annealed textures. Microprobe analyses of constituent minerals in 11 xenoliths indicate that bulk compositions of xenoliths are magnesian but with significant variability from xenolith to xenolith especially in Fe/Mg and Cr/Al ratios and in absolute amounts of Al₂O₃ and Cr₂O₃. Within any single xenolith, however, coexisting minerals are homogeneous and appear to be compositionally equilibrated. Geothermometry of coexisting orthopyroxene and augite indicates temperatures of equilibration of about 1100°C but there is considerable uncertainty in this estimate due to significant non-quadrilateral pyroxene substitutions. There is no accurate way to determine pressures, but the ubiquity of Cr-poor spinel and absence of garnet imply pressures less than about 15–20 kbar.The margins of most xenoliths show significant alteration through reaction with enclosing alkaline magma. Principal reaction features include zoning of spinels and olivines toward compositions in equilibrium with the magma, and reaction-melting of orthopyroxene to a symplectite of olivine plus silica-rich glass. Glass composition profiles across the symplectites indicate that alkalis, titanium and aluminum diffused into the symplectite from the magma and that silica diffused into the magma. All glass analyses show very low iron, magnesium and calcium.Xenolith mineral assemblages and chemistry indicate their origin in the upper mantle at relatively shallow depths. They are therefore not related genetically to the enclosing basanite magma which came from deeper in the mantle, but rather are accidental fragments of country rock picked up by magma on its way to the surface. The details of the reaction features strongly imply that the magma had partially crystallized by the time it reacted with xenoliths, possibly while still in the mantle.     

On the modelling of sand bedforms using the semivariogram

This study shows the usefulness of the semivariogram for modelling sand ripples created by water flows of varied flow intensity. A combination of two mathematical functions is fitted to each sample semivariogram, that is an exponential (or stochastic) component and a periodic component. The parameters of each of these components have direct physical meaning. A non-dimensional ratio combining the two parameters of the exponential model is interpreted as a regularity index (which increases with the degree of regularity of bedform arrangement). This regularity index is inversely related to the Froude number of the flow. The non-dimensional wavelength, estimated from the dominant periodic function, is also inversely and closely related to the Froude number. The wave height, accurately estimated from properties of the two fitted components, is a direct function of flow velocity and is also proportional to the standard deviation of bed elevations. The bedform shape introduces a considerable discrepancy between the generally assumed normal frequency distribution and the empirical distributions of bed height. The series of bed elevations are generally characterized by a mixture of normal distributions having the same variance but different means. The calculation of a covariance assuming a constant and single mean (as in spectral analysis) can therefore be misleading and the problem may be avoided by using the semivariogram.     

Estimation of aromatic hydrocarbons in seawater at proposed deepwater port (DWP) sites in the Gulf of Mexico

Approximately 100 water samples were collected from three different depths at the proposed deep water port sites in the Gulf of Mexico and analysed for aromatic hydrocarbons by fluorescence spectroscopy. Results indicated that the aromatic hydrocarbon concentrations in the water column decreased as one progresses from the surface water, through the water column, to the bottom sediments.