Twenty‐year weathering remeasurements at St Paul's Cathedral,London

Microerosion meter (MEM) measurements of the surface height of the balustrade of St Paul's Cathedral, London, have been repeated in the year 2000 following earlier measurements in 1980, 1981, 1985 and 1990. Methodological sources of error mean that while the measurements were made to 0·0001 mm, the data are reliable to two decimal places. There was a reduction in the mean erosion rate on horizontal sites from 0·045 mm a^?1 in the period 1980–1990 to 0·025 mm a^?1 in 1990–2000. Decreases in atmospheric SO₂ levels from 20–25 ppb in 1980–1982 to around 10 ppb in 1990–2000, offer a causal explanation. The surface topography evolved more erratically in 1990–2000 than before, with much, but not all, of the more microelevated areas showing greater, and often more variable erosion. There are also indications of less erosion and more surface rises in low‐lying microareas on horizontal sites which is interpreted as possible deposition and/or microfloral growth in wetter depressions, the pattern being largely absent on a well drained vertical site. Copyright © 2001 John Wiley & Sons, Ltd.     

Proterozoic low-sulfidation epithermal Au-Ag mineralization in the Mallery Lake area, Nunavut, Canada

The Mallery Lake area contains pristine examples of ancient precious metal-bearing low-sulfidation epithermal deposits. The deposits are hosted by rhyolitic flows of the Early Proterozoic Pitz Formation, but are themselves apparently of Middle Proterozoic age. Gold mineralization occurs in stockwork quartz veins that cut the rhyolites, and highest gold grades (up to 24 g/t over 30 cm) occur in the Chalcedonic Stockwork Zone. Quartz veining occurs in two main types: barren A veins, characterized by fine- to coarse-grained comb quartz, with fluorite, calcite, and/or adularia; and mineralized B veins, characterized by banded chalcedonic silica and fine-grained quartz, locally intergrown with fine-grained gold or electrum. A third type of quartz vein (C), which crosscuts B veins at one locality, is characterized by microcrystalline quartz intergrown with fine-grained hematite and rare electrum. Fluid inclusions in the veins occur in two distinct assemblages. Assemblage 1 inclusions represent a moderate temperature (Th=150 to 220 °C), low salinity (~1 eq. wt% NaCl, with trace CO₂), locally boiling fluid; this fluid type is found in both A and B veins and is thought to have been responsible for Au-Ag transport and deposition. Assemblage 2 inclusions represent a lower temperature (Th=90 to 150 °C), high salinity calcic brine (23 to 31 wt% CaCl₂-NaCl), which occurs as primary inclusions only in the barren A veins. Assemblage 1 and 2 inclusions occur in alternating quartz growth bands in the A-type veins, where they appear to represent alternating fluxes of dilute fluid and local saline groundwater. No workable primary fluid inclusions were observed in the C veins. The A-vein quartz yields '¹⁸O values from 8.3 to 14.5‰ (average=10.9ǃ.7‰ [1C], n=30), whereas '¹⁸O values for B-vein quartz range from 11.2 to 14.0‰ (average=13.0ǂ.9‰, n=12). Calculated '¹⁸O_H2O values for the dilute mineralizing fluid from B veins range from -2.6 to 0.2‰ (average=-0.8ǂ.9‰, n=12) and are consistent with a dominantly meteoric origin. No values could be calculated for the brine, however, because all A-vein quartz samples contain mixed fluid inclusion populations. However, the fact that A-vein quartz samples extend to lower '¹⁸O values than the B veins suggests that the brine had a lighter isotopic signature relative to the dilute fluid. Hydrogen isotopic ratios of fluid inclusion waters extracted from eleven quartz samples of both vein types range from 'D_FI=-56 to -134‰, but show no particular correlation with vein type. In most respects, the mineralogical and fluid characteristics of the Mallery Lake system are comparable to those of Phanerozoic low-sulfidation deposits, and although the presence of high salinity brines is unusual in such deposits, it is not unknown (e.g., Creede, Colorado). In addition, one of the few other examples of well-preserved, Precambrian, low-sulfidation epithermal deposits, from the Central Pilbara tectonic zone, Australia, contains a similarly bimodal fluid assemblage. The significance of these saline brines is not clear, but from this study we infer that they were not directly involved with Au-Ag transport or deposition.     

Air Quality,Climate, and Policy: A Case Study of Ozone Pollution in Tucson,Arizona

This article addresses the need to better understand the complex interactions between climate, human activities, vegetation responses, and surface ozone so that more informed air‐quality policy recommendations can be made. The impacts of intraseasonal climate variations on ozone levels in Tucson, Arizona from April through September of 1995 to 1998 are determined by relating variations in ozone levels to variations in atmospheric conditions and emissions of ozone's precursor chemicals, volatile organic compounds (VOCs) and nitrogen oxides (NO_x), and by determining month‐specific atmospheric conditions that are conducive to elevated ozone levels. Results show that the transport of ozone and its precursor chemicals within the Tucson area causes the highest ozone levels to be measured at a downwind monitor. The highest ozone levels occur in August, due in part to the presence of the North American monsoon. Atmospheric conditions conducive to elevated ozone concentrations differ substantially between the arid foresummer (May and June) and the core monsoon months ( July and August). Transport of pollution from Phoenix may have a substantial impact on elevated ozone concentrations during April, May, and June, while El Paso/Ciudad Juarez –derived pollution may contribute significantly to elevated ozone concentrations in August and September. Two broad policy implications derive from this work. Regional pollutant transport, both within the U.S. and between the U.S. and Mexico, is a potential issue that needs to be examined more intensively in future studies. In addition, spatiotemporal variations in sensitivities of ozone production require the adoption of both NO_x and VOC control measures to reduce ozone levels in the Tucson area.     

Constraints on crustal hydration below the Colorado plateau from Vp measurements on crustal xenoliths

Seismic velocities have been measured as a function of confining pressure to 8 kbar for crustal xenoliths from the Moses Rock Dike and Mule Ear Diatreme, two kimberlite pipes on the Colorado Plateau. Rock types measured include rhyolite, granite, diorite, metasedimentary schists and gneisses, mafic amphibolites and granulites. Many of our samples have been hydrothermally altered to greenschist facies mineral assemblages during transport to the earth's surface. The velocity of compressional waves measured on altered amphibolites and granulites are too low by 0.1–0.3 km/s for such rock types to be characteristic of deep crustal levels. A direct correlation exists between progressive alteration and the presence of microcracks extending into the xenoliths from the kimberlitic host rock. Velocities of pristine samples are compatible with existing velocity profiles for the Colorado Plateau and we conclude that the crust at depths greater than 15 km has probably not undergone a greenschist facies metamorphic event. The xenolith suite reflects a crustal profile similar to that exposed in the Ivrea-Verbano and Strona-Ceneri zones in northern Italy.     

Proton and Cd adsorption onto natural bacterial consortia: Testing universal adsorption behavior

Bacterial surface adsorption can control metal distributions in some natural systems, yet it is unclear whether natural bacterial consortia differ in their adsorption behaviors. In this study, we conduct potentiometric titration and metal adsorption experiments to measure proton and Cd adsorption onto a range of bacterial consortia. We model the experimental data using a surface complexation approach to determine thermodynamic stability constants. Our results indicate that these consortia adsorb similar extents of protons and Cd and that the adsorption onto all of the consortia can be modeled using a single set of stability constants. Consortia of bacteria cultured from natural environments also adsorb metals to lesser extents than individual strains of laboratory-cultivated species. This study suggests that a wide range of bacterial species exhibit similar adsorption behaviors, potentially simplifying the task of modeling the distribution and speciation of metals in bacteria-bearing natural systems. Current models for bacteria-metal adsorption that rely on pure strains of laboratory-cultivated species likely overpredict the amount of bacteria-metal adsorption in natural systems.