Geothermal resource assessment of the United States

Geothermal resource assessment is the broadly based appraisal of the quantities of heat that might be extracted from the earth and used economically at some reasonable future time. In the United States, the Geological Survey is responsible for preparing geothermal assessments based on the best available data and interpretations. Updates are required every few years owing to increasing knowledge, enlarging data base, improving technology, and changing economics. Because geothermal understanding is incomplete and rapidly evolving, the USGS complements its assessments with a broad program of geothermal research that includes (1) study of geothermal processes on crustal and local scales, (2) regional evaluations, (3) intensive study of type systems before and during exploitation (4) improvement of exploration techniques, and (5) investigation of geoenvironmental constraints.     

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.     

A general mixing equation with applications to Icelandic basalts

The mixing equation applied by Vollmer [1] to Pb and Sr isotope ratios is shown to be a general equation applicable to consideration of element and isotope ratios. The mixing equation is hyperbolic and has the form:Ax + Bxy + Cy + D = 0where the coefficients are dependent on the type of plot considered: i.e. ratio-ratio, ratio-element, or element-element. Careful use of this equation permits testing whether mixing is a viable process, places constraints on end member compositions, allows distinction between mixing of sources and mixing of magmas, and should allow distinction between recent mixing and long-term evolution of sources.The available chemical data for postglacial basalts from Iceland and along the Reykjanes Ridge are not consistent with either mixing of magmas or simple mixing of an enriched ocean island source with a depleted ocean ridge source. If the available analyses for basalts are representative of the source regions, the data are consistent with at least two models neither of which can be properly tested with the available data.(1) There are two separate mixing trends: one beneath Iceland with the alkali basalt source and a depleted Iceland source as end members; the second along the Reykjanes Ridge with a heterogeneous ocean ridge basalt source and a source similar to that for intermediate basalts on Iceland as end members. The depleted Iceland source and the depleted ocean ridge source are not the same.(2) The chemistry of the basalts is not determined by mixing. Instead the basalts are derived from a multiplicity of sources with a similar history which have been isolated for hundreds of millions of years.     

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.     

In situ uptake of mercury by the intertidal mussel,Mytilus californianus

The in situ uptake of mercury in tissues of Mytilus californianus was studied by exposing control specimens to waters at four depths near a submarine wastewater discharge for a period of 24 weeks. The response patterns observed for digestive gland, adductor muscle and gonadal tissues were strikingly different. Digestive gland concentrations increased rapidly to the heightened levels found for indigenous specimens. On the other hand, changes in the mercury content of adductor muscle were not statistically significant, and gonadal tissues generally exhibited a low rate of increase. No correlation with depth was observed.     

Lead and copper in the waters of Raritan and Lower New York Bays

A survey of waters adjacent to this heavily urbanized and industrialized region showed concentrations of copper, 65 μg l.^?1 to be the highest reported to date for estuarine waters, and lead up to 13.9 μg l.^?1 Correlations between distributions of dissolved and total metal concentration in the water column, hydrography, and metal in the sediment were related to benthic studies in this area. Laboratory studies are cited which show the potential for adverse effects on marine animals at these metal concentrations.     

Petrogenesis of Archaean ultrabasic and basic volcanics: Evidence from rare earth elements

Rare earth element (REE) and major element data are presented on 44 Archaean samples which include spinifex textured ultramagnesian lavas (STPK) spinifex textured basalts (STB) and low MgO tholeiites. The samples come from the Yilgarn and Pilbara Blocks (W. Australia), Barberton (South Africa), Belingwe and Que Que (Rhodesia), Abitibi (Canada) and the 3.7 b.y. Isua Belt of Western Greenland. In addition REE data are given on three near primitive mid-ocean ridge basalts (MORB) and a glassy MORB-type basalt from Taiwan. We suggest that REE patterns, particularly the light REE and Eu, can be affected by metamorphism, but argue that the consistency of pattern from samples both within and between areas enables recognition of primary patterns. La/Sm ratios of 2.7 b.y. STPK are characterised by being lower than those of associated basalts. The 3.5 b.y. STPK Barberton material does not show this feature but instead displays significant heavy REE depletion. The separation of garnet from these liquids is suggested as a possible mechanism for the high CaO/Al₂O₃ ratios, (Al loss) and the heavy REE and Sc depletion. The REE data on Barberton material is equivocal on the derivation of the so-called basaltic komatiites from the peridotitic komatiites. However, REE analyses on STPK and high magnesian lavas from elsewhere suggests that crystal fractionation is not a viable mechanism to produce one from the other. We suggest instead, that varying amounts of partial melting of different sources is responsible for the spectrum of compositions. The STB appear to be an easily recognised rock type within the Archaean. They are characterised by quench (clinopyroxene) textures and a light REE enriched pattern. It is suggested that these are near primary melts and that their REE patterns mirror their mantle source. We propose a two stage model for the 2.7 b.y. mafic complexes, in which, prior to the generation of ultrabasic magmas, the source underwent a small amount of partial melting which resulted in the removal of a melt enriched in incompatible elements. The depletion process could be achieved either during mantle diapirism or by upward migration of interstitial melts into an Archaean low velocity zone. The spread of La/Sm ratios in STPK and STB is used as an argument that the Archaean mantle was chemically heterogeneous and that the degree of heterogeneity was similar to that observed in modern ocean volcanics. As a result, partial melting of the mantle under different P-T conditions produced a spectrum of magma types. The information presently available on Archaean mafic and silicic magmatism and the incompleteness of geochemical data on present day tectonic environments are two major obstacles in formulating Archaean tectonic models. In addition a comparison of present day and Archaean ultramafic and silicic rocks suggests that plate tectonic models as presently understood may not be suitable analogues for all Archaean tectonic environments.     

Resistance of quartz silt to isotopic exchange under burial and intense weathering conditions

Oxygen isotopic compositions of quartz from silty sediments buried to 5400 m depth from two wells in the Gulf of Mexico each showed δ5¹⁸O variations of less than 1.7%. Clay diagenesis has been reported within this depth. The observed variations in the quartz do not appear to be primarly diagenetic effects, but rather are mainly depositional features reflecting variations in the sources of the sediments. Sources may be influenced by the variation of distance from the shore at different depths in a given sampling location and by sediment production by continental glaciations. Stability of the oxygen isotopic composition of quartz in the 10–20 μm size range under long-time humid, temperate weathering conditions was studied by analysis of saprolites formed from Pennsylvanian to Precambrian crystalline rocks. In four of the five cases, the 10–20 μm fraction was found to have only 0.1–0.5%. greater δ¹⁸O than the corresponding 20–50 μm fraction. This increase may be attributable either to a slight oxygen isotopic exchange with ambient ground waters or original differences within the rock since the saprolites were sufficiently coherent to make an influx of extraneous detrital silt unlikely. The amount of oxygen isotopic exchange in silt size quartz over periods of many million years of shallow burial or weathering appears to be small enough to permit the use of the oxygen isotopic ratio of quartz in tracing the origin of eolian and fluvial additions of minerals to continental soils and pelagic sediments.