A 20 cm2 CCD mosaic camera for a dark matter search part I : Mechanics,optics and cryogeny

A 20cm ² CCD mosaic camera has been especially built to search for dark galactic halo objects by the gravitational microlensing effect. The sensitive area is made of 16 edge-buttable CCDs developped by Thomson-CTS, with 23×23 µm ² pixels. The 35 kg camera housing and mechanical equipment is presented. The associated electronics and data acquisition system are described in a separate paper. The camera resides at the focal plane of a 40 cm, f/10, Ferson reflector. The instrument has been in operation since December 1991 at the La Silla Observatory (ESO).     

Experimental investigation of the effects of temperature and ionic strength on Mo isotope fractionation during adsorption to manganese oxides

The Mo stable isotope system is being applied to study changes in ocean redox. Such applications implicitly assume that Mo isotope fractionation in aqueous systems is relatively insensitive to frequently changing environmental variables such as temperature (T) and ionic strength (I). A major driver of fractionation is the adsorption of Mo to Mn oxyhydroxide surfaces [Barling J. and Anbar A. D. (2004) Molybdenum isotope fractionation during adsorption by manganese oxides. Earth Planet. Sci. Lett.217(3-4), 315-329]. Here, we report the results of experiments that determine the extent to which Mo isotope fractionation during adsorption of Mo to the Mn oxyhydroxide mineral birnessite is sensitive to T and I. The results are compared to new predictions from quantum chemical computations. We measured fractionation from 1 to 50 °C at I = 0.1 m and found that Δ^97/95Mo_{dissolved-adsorbed} varies from 1.9‰ to 1.6‰ over this temperature range. Experiments were also performed at 25 °C in synthetic seawater (I = 0.7); fractionation at this condition was the same within analytical error as in low ionic strength experiments. These findings confirm that the Mo isotope fractionation during adsorption to Mn oxyhydroxides is relatively insensitive to variations and T and I over environmentally relevant ranges. To relate these findings to potential mechanisms of Mo isotope fractionation, we also report results for density functional theory computations of the fractionation between and various possible structures of molybdic acid as a function of temperature. Because no plausible species fractionates from with a magnitude matching the experiments, we are left with three possibilities to explain the fractionation: (1) solvation effects on the vibrational frequencies of aqueous species considered thus far are significant, such that our calculations in vacuo yield inaccurate fractionations; (2) a trace aqueous species not yet considered fractionates from and then adsorbs to birnessite; or (3) a surface complex not present in solution forms on birnessite in which Mo is not tetrahedrally coordinated. Our findings help validate assumptions underlying paleoceanographic applications of the Mo isotope system and also lead us closer to understanding the mechanism of isotope fractionation during adsorption of Mo to Mn oxyhydroxides.     

The hydrochemistry of a semi-arid pan basin case study: Sua Pan,Makgadikgadi, Botswana

This study presents results on the fluid and salt chemistry for the Makgadikgadi, a substantial continental basin in the semi-arid Kalahari. The aims of the study are to improve understanding of the hydrology of such a system and to identify the sources of the solutes and the controls on their cycling within pans. Sampling took place against the backdrop of unusually severe flooding as well as significant anthropogenic extraction of subsurface brines. This paper examines in particular the relationship between the chemistry of soil leachates, fresh stream water, salty lake water, surface salts and subsurface brines at Sua Pan, Botswana with the aim of improving the understanding of the system’s hydrology. Occasionally during the short wet season (December–March) surface water enters the saline environment and precipitates mostly calcite and halite, as well as dolomite and traces of other salts associated with the desiccation of the lake. The hypersaline subsurface brine (up to TDS 190,000 mg/L) is homogenous with minor variations due to pumping by BotAsh mine (Botswana Ash (Pty) Ltd.), which extracts 2400 m³ of brine/h from a depth of 38 m. Notable is the decrease in TDS as the pumping rate increases which may be indicative of subsurface recharge by less saline water. Isotope chemistry for Sr (⁸⁷Sr/⁸⁶Sr average 0.722087) and S (δ³⁴S average 34.35) suggests subsurface brines have been subject to a lithological contribution of undetermined origin. Recharge of the subsurface brine from surface water including the Nata River appears to be negligible.     

Stable isotope study of antimony deposits in the Muratdagi region,western Turkey

The Muratdagi region is rich in antimony deposits having the following common characteristics: post Miocene age, location on the down-thrown blocks next to normal faults, in the vicinity of active or fossil thermal springs, and in contact with carbonate rocks. The isotopic composition of — 7. SMOW of the mineralizing fluid calculated from the measured ° ¹⁸O of quartz and the fluid inclusion microthermometry, is indicative of meteoric water origin. The ° ¹³C of the inclusion CO₂ of — 19.1 to — 25.4 PDB is indicative of interaction with organic material-graphite. The ° ³⁴S of stibnite — 3.6 to — 0.7 is, in view of the mineral assemblage, indicative of magmatic origin of the sulphur. A tightly confined set of structural, lithological, hydrological and geochemical features define a sequence of geochemical processes; formation of acid and reducing fluid, leaching and transport of antimony complexes and precipitation of stibnite within defined lithological units. The set of processes seems to have taken place within a space of 5000 m lateral and 1000 m vertical extension.     

A 20cm 2 CCD mosaic camera for a dark matter search part II : Electronics,data acquisition and performance

Conclusion To summarize, the readout and the control system of the CCD mosaic camera are running since December 1991 at the La Silla Observatory (ESO). The overall performance of the camera has been good. About 12000 pictures (data and flat-fields) have been successfully registered up to now. We will report in the near future preliminary scientific results of the EROS experiment.     

Electron spin resonance of stabilized free radicals in sedimentary organic matter

Electron spin resonance (ESR) is evaluated as a method to study the thermal degradation of sedimentary organic matter which consists mainly of kerogen. Whole rock and separated kerogen samples were pyrolysed stepwise (ambient to 700°C at 50°C increments), extracted and analysed for elemental composition and ESR spectra at each step. Whole rock samples give rise to complex spectra which include those of paramagnetic metals and are therefore unsuitable in most cases for this purpose.The ESR parameters g value, ΔH and N_g differ for different types of immature organic matter. An increase in N_g,shift of g value to 2.0026–2.0028 and reduction in h are the main trends during pyrolysis and in natural heating of sedimentary organic matter.The peak generations of liquid and gaseous hydrocarbons coincide with maxima of free radical density. ESR spectroscopy in combination with complementary geochemical characterization of the sedimentary organic matter can serve to indicate maturity with respect to peak oil-gas generation.     

Sulphur, carbon and oxygen isotope studies of early Variscan mineralisation and Pb-Sb vein deposits in the Cornubian orefield: implications for the scale of fluid movements during Variscan deformation

The strongly deformed Middle Devonian-Lower Carboniferous metasedimentary-volcanic successions of the Trevone Basin (SW England) contain stratiform and Pb-Sb vein deposits that reveal a wide variation in δ³⁴S and δ¹³C, reflecting mineral deposition during diagenesis, regional metamorphism and basin inversion. Pre-Variscan metasedimentary sulphide (δ³⁴S=−33.7 to −26.7‰) and metabasite sulphide (δ³⁴S=+4.0 to +10.8‰) suggest two accessible source reservoirs for sulphur which were available for Sb-As-(Au) and Pb-Zn-(Ag) mineralisation (δ³⁴S=−3.3 to −15.0‰) during late Variscan semiductile-brittle shear. On the basis of pressure-corrected fluid inclusion temperatures, the calculated composition of fluid sulphur reveals an enrichment in δ³⁴S_H2S in the individual vein parageneses and depletion of the fluid sulphur reservoir during evolution of the vein systems. Carbonates in the same veins are partly contemporaneous with Pb-Sb mineralisation and late tensional deformation; their isotopic composition (δ¹³C=−3.2 and −13.4‰) appears strongly influenced by the host formation. Fluid inclusions in post-tensional quartz show a marked reduction in CO₂, suggesting that episodes of CO₂ degassing in response to punctuated reductions in pressure during uplift and brittle deformation was an important mechanism for vein carbonation. An origin for the Pb-Sb mineralisation involving local remobilisation of sulphur from the mixed metasedimentary-volcanic succession is probably inseparable from processes connected with Variscan metamorphism and deformation. Although the N Cornish Variscan deformation is part of a spatially large-scale event, the isotopic evidence suggests compartmentalisation of sulphur and carbon isotope features and short distances between sources and sinks. Received: 15 August 1998 / Accepted: 8 October 1999     

SHRIMP zircon U-Pb ages from coal beds across the Permian-Triassic boundary,eastern Yunnan,southwestern China

The first SHRIMP zircon U e Pb ages from coal beds close to the end-Permian mass extinction are reported from the C_1 coal seam in the Yantang Mine in Laibin Town, Xuanwei County, eastern Yunnan Province.Zircons were extracted from kaolinite claystone layers, defined as tonsteins(volcanic ash deposits), in the subseam B_1 and B_3 of the coal seam C_1.The U-Pb ages are 252.0 ± 2.3 Ma and 250.3 ± 2.1 Ma for the sub-seam B_1 and B_3, respectively. Within analytical uncertainties, these U-Pb ages include the time period of the onset of the mass extinction at 251.941 ± 0.037 Ma, which was obtained from the marine Meishan section in Zhejiang Province, ~1600 km away from the Yantang Mine. These new ages represent not only the first and closest ages to the PTB mass extinction in terrestrial coal beds, but also ages from the nearest site to the Emeishan volcanoes investigated so far. Therefore these new data provide the most accurate stratigraphic horizon of terrestrial facies of the end-Permian extinction in South China. The Emeishan volcanoes were likely the source of volcanic ash in the coal seams at the Xuanwei County and broader areas in South China. Furthermore, the minerals and geochemistry characteristics of the C_1 coal seam also implied the influences of contemporaneous volcanic activities.     

Sulfur isotope study of source and deposits of stibnite in the Turhal Area,Turkey

The Turhal antimony sulfide ore deposits are hosted by a Permian-Jurassic sequence which consists of black phyllites at the base followed by interbedded phyllites and calcareous quartzites with metabasite interlayers and then by brown-gray phyllites with marble blocks. Four different styles and three distinct episodes of mineralization were distinguished according to deposition features of the ores and kinkbands in the stibnite crystals. Stibnite from stratiform, disseminated and vein occurrences as well as pyrite from black phyllites showed the following sulfur isotope composition (³⁴S): +2.8 and +3.0 for stratiform stibnite (n = 2), +3.6 and +5.5 for disseminated stibnite (n = 2), +2.5 to +7.8 for vein stibnite (n = 11) and -6.1 to +0.1 for pyrite (n = 3). The ³⁴S compositions of stibnite are interpreted as suggesting an ultimately single source for sulfur in the various styles of mineralization, i.e. synsedimentary volcanic exhalations for the stratiform and disseminated together with ores and hydrothermal mobilisation of these as well as leaching of volcanic rocks to form the vein ores. Deep basinal fluids probably under normal geothermal gradient conditions caused the leaching of the primary sulfides as suggested by the oxygen isotope composition of vein quartz associated with the ores. By contrast sulfur in pyrite is essentially a derivation of seawater sulfate through bacterial and/or chemical reduction.     

Lacustrine sediments and lichen transplants: two contrasting and complimentary environmental archives of natural and anthropogenic lead in the South Urals, Russia

Lead (Pb) concentrations and isotope ratios of two different geochemical archives are compared; lake sediment cores and lichens (Hypogymnia physodes, naturally growing and transplanted) from a ca. 80 km-long transect centred on the Cu smelter and former mining town of Karabash, Ural Mountains, Russia. Lead concentrations in sediment cores from 10 lakes were generally low near their base and show an abrupt increase in their upper portions interpreted to coincide with the onset of large-scale smelting operations in 1910. Lead isotope ratios derived from ²⁰⁴Pb, ²⁰⁶Pb, ²⁰⁷Pb, ²⁰⁸Pb of the bottom layers differed significantly from those of the top. The top sediments have isotope ratios that show distinct end members, one of which was the stack dust from the Karabash smelter, which is similar to the Pb derived from ores from Sibay, a major mine in the Urals. The composition of the bottom sediment layers generally fall slightly off a mixing line between the top sediments and average Earth’s upper crust. Lichens transplanted from a reference site, as well as naturally growing lichens, sampled from southwest of the smelter have isotope ratios similar to those of the stack dust. Lichens to the northeast contained Pb from the smelter, but are increasingly influenced by other sources probably leaded petrol and local soils, and a signature derived from a source enriched in ²⁰⁷Pb. Vegetables collected from local kitchen gardens contained Pb from an additional atmospheric source, possibly coal. Our work confirms that: (1) Pb isotopes in lake sediments provide a long-term record of inputs and allows the characterisation of natural and anthropogenic sources; (2) Pb isotopes in lichens provide a short-term record of local and long-range atmospheric deposition at high spatial resolution and short time scales as they replace their Pb content within a few months; (3) determination of all four stable Pb isotopes is necessary for the identification of the sources of Pb and is extremely sensitive for discerning minor source signatures, even in an area with a dominant source such as a smelter. Particularly significant for the Karabash area is that ore-smelter-derived airborne Pb is a major component in the lake sediments and lichens but its contribution reaches insignificant levels ca. 40 km from the smelter.