Pentobarbital Found in Ground Water     

William P. Eckel  Benjamin Ross  Robert K. Isensee 《Ground water》1993,31(5):801-804

  相似文献   

Equilibrium coexistence of three amphiboles     

Peter Robinson  Howard W. Jaffe  Cornelis Klein Jr.  Malcolm Ross 《Contributions to Mineralogy and Petrology》1969,22(3):248-258

Electron probe and wet chemical analyses of amphibole pairs from the sillimanite zone of central Massachusetts and adjacent New Hampshire indicated that for a particular metamorphic grade there should be a restricted composition range in which three amphiboles can coexist stably. An unequivocal example of such an equilibrium three amphibole rock has been found in the sillimanite-orthoclase zone. It contains a colorless primitive clinoamphibole, space group P2₁/m, optically and chemically like cummingtonite with blue-green hornblende exsolution lamellae on (100) and (¯101) of the host; blue-green hornblende, space group C2/m, with primitive cummingtonite exsolution lamellae on (100) and (¯101) of the host; and pale pinkish tan anthophyllite, space group Pnma, that is free of visible exsolution lamellae but is a submicroscopic intergrowth of two orthorhombic amphiboles. Mutual contacts and coarse, oriented intergrowths of two and three host amphiboles indicate the three grew as an equilibrium assemblage prior to exsolution. Electron probe analyses at mutual three-amphibole contacts showed little variation in the composition of each amphibole. Analyses believed to represent most closely the primary amphibole compositions gave atomic proportions on the basis of 23 oxygens per formula unit as follows: for primitive cummingtonite (Na_0.02Ca_0.21 ^– Mn_0.06Fe²⁺ _2.28Mg_4.12Al_0.28) (Al_0.17Si_7.83), for hornblende (Na_0.35Ca_1.56Mn_0.02Fe_1.71Mg_2.85Al_0.92) (Al_1.37Si_6.63), and for anthophyllite (Na_0.10Ca_0.06Mn_0.06Fe_2.25Mg_4.11Al_0.47) (Al_0.47Si_7.53). The reflections violating C-symmetry, on X-ray single crystal photographs of the primitive cummingtonite, are weak and diffuse, and suggest a partial inversion from a C-centered to a primitive clinoamphibole. Single crystal photographs of the anthophyllite show split reflections indicating it is an intergrowth of about 80% anthophyllite and about 20% gedrite which differ in their b crystallographic dimensions. Split reflections are characteristic of all analyzed orthorhombic amphiboles so far examined from Massachusetts and New Hampshire except the most aluminous gedrites, and the relative intensity of the gedrite reflections is roughly proportional to the degree of Na and Al substitution. Thin sections of a few of these anthophyllite specimens show lamellae parallel to (010) that are just resolved with a high power objective.Publication approved by the Director, U.S. Geological Survey.  相似文献   

Tektites: A post-Apollo view     

Stuart Ross Taylor 《Earth》1973,9(2):101-123

Prior to the receipt of the lunar samples, it was the scientific consensus that tektites were melted and splashed material formed during large cometary or meteorite impact events. Whether the impact took place on the Earth or the Moon was the topic of a long-standing scientific debate, which raged with particular intensity during the decade previous to the lunar landings.Four definite and separate tektite-strewn fields are known: bediasites (North America, 34 m.y.); moldavites (Czechoslovakia, 14 m.y.); Ivory Coast (1.3 m.y.); and Southeast Asian and Australian fields (0.7 m.y.). A fifth possible occurrence, of high-Na australites, possibly 3–4 m.y. old, remains to be substantiated. The age of infall of the australites is not agreed upon. Radiometric and fission track dates agree with the magnetic stratigraphy for deep-sea core microtektite occurrences at about 0.7 m.y. Terrestrial stratigraphic evidence favours a recent (30,000 years) date.The chemistry of tektites appears to reflect that of the parent material, and losses during fusion appear to be restricted to elements and compounds more volatile than cesium. Terrestrial impact glasses provide small-scale analogues of tektite-forming events, and indicate that only the most volatile components are lost during fusion.The Apollo lunar missions provide critical evidence which refutes the hypothesis of lunar origin of tektites. Tektite chemistry is totally distinct from that observed in lunar maria basalts. These possess Cr contents which are two orders of magnitude higher than tektites, distinctive REE patterns with large Eu depletions, high Fe and low SiO₂ contents, low K/U ratios and many other diagnostic features, none of which are observed in the chemistry of tektites. The lunar uplands compositions, as shown by Apollo 14, 15 and 16 samples and the μ-ray and XRF orbiter data, are high-Al, low-SiO₂ compositions totally dissimilar to those of tektites. The composition of lunar rock 12013 shows typical lunar features and is distinct from that of tektites. The small amounts of lunar K-rich granitic material found in the soils have K/Mg and K/Na ratios 10–50 times those of tektites.The ages of the lunar maria (3.2–3.8 aeons) and uplands (> 4.0 aeons) are an order of magnitude older than the parent material of the Southeast Asian and Australian tektites, which yield Rb-Sr isochrons indicating ages of the order of 100–300 m.y. The lunar lead isotopic compositions are highly radiogenic whereas tektites have terrestrial Pb isotopic ratios. Lunar δ¹⁸ O values are low (< 7 per mil) compared with values of +9.6 to +11.5 per mil for tektites. In summary, a lunar impact origin for tektites is not compatible with the chemistry, age or isotopic composition of the lunar samples. A lunar volcanic origin, recently revived by O'Keefe (1970) encounters most of the same problems. Recent lunar volcanism (< 50 m.y.), if the source of tektites, should contribute tektite glass to the upper layers of the regolith. None has been found. The presence of meteoritic components in tektites, and the high pressure phase coesite, are more readily interpreted as evidence of impact.The element abundances and inter-element variations in tektites do not resemble those in terrestrial igneous rocks, but show a close similarity to terrestrial sandstones. The composition of the Southeast Asian tektites, australites and moldavites resembles that of micaceous sandstones or subgreywackes, the Ivory Coast tektite composition is similar to that of greywacke, and the bediasite chemistry is analogous to that of arkose.No suitable terrestrial impact site has been identified for the bediasites, Southeast Asian tektites and australites. It is suggested that a search for the source of these latter strewnfields be made using satellite photographs to look for wide shallow craters produced by super-Tunguska type events on areas of Mesozoic sandstones. The moldavites were possibly formed during the Ries Crater event but, if so, the precise source of the material remains to be identified. The Ivory Coast tektites are linked by chemistry, isotope and age evidence to the Bosumtwi Crater, Ghana. The overall evidence now supports the origin of tektites by cometary (or meteorite) impact on terrestrial sedimentary rocks.  相似文献   

Observations from space of the solar corona/inner zodical light     

R.M. Macqueen  C.L. Ross  T. Matingly 《Planetary and Space Science》1973,21(12):2173-2176

Observations, from the Apollo 16 Spacecraft, in lunar orbit, of the total radiance of the K + F corona, from 3 R to 55 R are presented and discussed.

The logarithmic slope of the K + F coronal radiance, in the region r > 20 R, is found to be n = 1.93, slightly less steep than previous determinations. The photometric axis of the radiance is found to be displaced 3 ± 1° north of the ecliptic, for the region r > 20 R, and this displacement is interpreted as an annual variation due to non-coincidence of the ecliptic and the symmetry axis of the zodiacal cloud.  相似文献   

Geochemistry and magmatic properties of eruption episodes from Haroharo linear vent zone, Okataina Volcanic Centre, New Zealand during the last 10 kyr     

Victoria C. Smith  Phil Shane  Ian A. Nairn  Catherine M. Williams 《Bulletin of Volcanology》2006,69(1):57-88

Post-10 ka rhyolitic eruptions from the Haroharo linear vent zone, Okataina Volcanic Centre, have occurred from several simultaneously active vents spread over 12 km. Two of the three eruption episodes have tapped multiple compositionally distinct homogeneous magma batches. Three magmas totalling ~8 km³ were erupted during the 9.5 ka Rotoma episode. The most evolved Rotoma magma (SiO₂=76.5–77.9 wt%, Sr=96–112 ppm) erupted from a southeastern vent, and is characterised by a cummingtonite-dominant mineralogy, a temperature of 739±14°C, and fO₂ of NNO+0.52±0.11. The least evolved (SiO₂=75.0–76.4 wt%, Sr=128–138 ppm, orthopyroxene+ hornblende-dominant) Rotoma magma erupted from several vents, and was hotter (764±18°C) and more reduced (NNO+0.40±0.13). The ~11 km³ Whakatane episode occurred at 5.6 ka and also erupted three magmas, each from a separate vent. The most evolved (SiO₂=73.3–76.2 wt%, Sr=88–100 ppm) Whakatane magma erupted from the southwestern (Makatiti) vent and is cummingtonite-dominant, cool (745±11°C), and reduced (NNO+0.34±0.08). The least evolved (SiO₂=72.8–74.1 wt%, Sr=132–134 ppm) magma was erupted from the northeastern (Pararoa) vent and is characterised by an orthopyroxene+ hornblende-dominant mineralogy, temperature of 764±18°C, and fO₂ of NNO+0.40±0.13. Compositionally intermediate magmas were erupted during the Rotoma and Whakatane episodes are likely to be hybrids. A single ~13 km³ magma erupted during the intervening 8.1 ka Mamaku episode was relatively homogeneous in composition (SiO₂=76.1–76.8 wt%, Sr=104–112 ppm), temperature (736±18°C), and oxygen fugacity (NNO+0.19±0.12). Some of the vents tapped a single magma while others tapped several. Deposit stratigraphy suggests that the eruptions alternated between magmas, which were often simultaneously erupted from separate vents. Both effusive and explosive activity alternated, but was predominantly effusive (>75% erupted as lava domes and flows). The plumbing systems which fed the vents are inferred to be complex, with magma experiencing different conditions in the conduits. As the eruption of several magmas was essentially concurrent, the episodes were likely triggered by a common event such as magmatic intrusion or seismic disturbance.  相似文献   

Site Response in Las Vegas Valley, Nevada from NTS Explosions and Earthquake Data     

Arthur Rodgers  Hrvoje Tkalcic  David McCallen  Shawn Larsen  Catherine Snelson 《Pure and Applied Geophysics》2006,163(1):55-80

We report site response in Las Vegas Valley (LVV) from historical recordings of Nevada Test Site (NTS) nuclear explosions and earthquake recordings from permanent and temporary seismic stations. Our data set significantly improves the spatial coverage of LVV over previous studies, especially in the northern, deeper parts of the basin. Site response at stations in LVV was measured for frequencies in the range 0.2–5.0 Hz using Standard Spectral Ratios (SSR) and Horizontal-Vertical Spectral Ratios (HVR). For the SSR measurements we used a reference site (approximately NEHRP B ``rock' classification) located on Frenchman Mountain outside the basin. Site response at sedimentary sites is variable in LVV with average amplifications approaching a factor of 10 at some frequencies. We observed peaks in the site response curves at frequencies clustered near 0.6, 1.2 and 2.0 Hz, with some sites showing additional lower amplitude peaks at higher frequencies. The spatial pattern of site response is strongly correlated with the reported depth to basement for frequencies between 0.2 and 3.0 Hz, although the frequency of peak amplification does not show a similar correlation. For a few sites where we have geotechnical shear velocities, the amplification shows a correlation with the average upper 30-meter shear velocities, V₃₀. We performed two-dimensional finite difference simulations and reproduced the observed peak site amplifications at 0.6 and 1.2 Hz with a low velocity near-surface layer with shear velocities 600–750 m/s and a thickness of 100–200 m. These modeling results indicate that the amplitude and frequencies of site response peaks in LVV are strongly controlled by shallow velocity structure.  相似文献   

Past and future polar amplification of climate change: climate model intercomparisons and ice-core constraints   总被引：1，自引：0，他引：1  

V. Masson-Delmotte  M. Kageyama  P. Braconnot  S. Charbit  G. Krinner  C. Ritz  E. Guilyardi  J. Jouzel  A. Abe-Ouchi  M. Crucifix  R. M. Gladstone  C. D. Hewitt  A. Kitoh  A. N. LeGrande  O. Marti  U. Merkel  T. Motoi  R. Ohgaito  B. Otto-Bliesner  W. R. Peltier  I. Ross  P. J. Valdes  G. Vettoretti  S. L. Weber  F. Wolk  Y. Yu 《Climate Dynamics》2006,27(4):437-440

  相似文献   

Decoupling of arsenic and iron release from ferrihydrite suspension under reducing conditions: a biogeochemical model     

André Burnol  Francis Garrido  Philippe Baranger  Catherine Joulian  Marie-Christine Dictor  Françoise Bodénan  Guillaume Morin  Laurent Charlet 《Geochemical transactions》2007,8(1):12

High levels of arsenic in groundwater and drinking water are a major health problem. Although the processes controlling the release of As are still not well known, the reductive dissolution of As-rich Fe oxyhydroxides has so far been a favorite hypothesis. Decoupling between arsenic and iron redox transformations has been experimentally demonstrated, but not quantitatively interpreted. Here, we report on incubation batch experiments run with As(V) sorbed on, or co-precipitated with, 2-line ferrihydrite. The biotic and abiotic processes of As release were investigated by using wet chemistry, X-ray diffraction, X-ray absorption and genomic techniques. The incubation experiments were carried out with a phosphate-rich growth medium and a community of Fe(III)-reducing bacteria under strict anoxic conditions for two months. During the first month, the release of Fe(II) in the aqueous phase amounted to only 3% to 10% of the total initial solid Fe concentration, whilst the total aqueous As remained almost constant after an initial exchange with phosphate ions. During the second month, the aqueous Fe(II) concentration remained constant, or even decreased, whereas the total quantity of As released to the solution accounted for 14% to 45% of the total initial solid As concentration. At the end of the incubation, the aqueous-phase arsenic was present predominately as As(III) whilst X-ray absorption spectroscopy indicated that more than 70% of the solid-phase arsenic was present as As(V). X-ray diffraction revealed vivianite Fe(II)₃(PO₄)₂.8H₂O in some of the experiments. A biogeochemical model was then developed to simulate these aqueous- and solid-phase results. The two main conclusions drawn from the model are that (1) As(V) is not reduced during the first incubation month with high Eh values, but rather re-adsorbed onto the ferrihydrite surface, and this state remains until arsenic reduction is energetically more favorable than iron reduction, and (2) the release of As during the second month is due to its reduction to the more weakly adsorbed As(III) which cannot compete against carbonate ions for sorption onto ferrihydrite. The model was also successfully applied to recent experimental results on the release of arsenic from Bengal delta sediments.  相似文献   

Platinum-group elements (Ir,Pd, Pt and Rh) in road-deposited sediments in two urban watersheds,Hawaii     

Ross A. Sutherland  D. Graham Pearson  Chris J. Ottley 《Applied Geochemistry》2007

This study represents the first detailed investigation of platinum-group elements (PGEs) in road-deposited sediment (RDS) in Hawaii, USA. Thirty-three sample locations, in two urban watersheds in Honolulu, Oahu, Hawaii were sampled. The <63 μm fraction of RDS was digested with aqua regia, followed by matrix separation with Dowex AG50-X8 cation exchange resin. PGEs were analyzed with inductively coupled plasma-mass spectrometry (ICP-MS) equipped with a desolvating nebulizer. Concentrations of Rh, Pd and Pt in residential streets reached 64, 105 and 506 ng/g, respectively. Maximum enrichment ratios, computed as RDS concentrations relative to baseline values, exceeded 400, indicating a significant anthropogenic signal with the sequence Rh > Pt > Pd. Iridium concentrations were uniformly low <1 ng/g, and enrichment ratios support a geogenic source. Significant interelement PGE correlations (Pd–Pt–Rh), combined with the magnitude of PGE pair-wise ratios (Pt/Pd, Pt/Rh and Pd/Rh), and relative percentages comparable to European RDS and roadside soil in Indiana, USA all suggest an automobile source. Attrition of PGE-loaded automobile catalytic converters and subsequent loss to the environment by exhaust emissions explains the significant environmental signal of PGEs in road environments of Hawaii. Further PGE work is required to quantify urban transport paths as PGEs are known to bioaccumulate, cause cellular damage and may have detrimental human health effects.  相似文献   

Improved seasonal climate forecasts for the Caribbean region using the Florida State University Synthetic Superensemble     

R. S. Ross  A. Chakraborty  A. Chen  L. Stefanova  S. Sirdas  T. N. Krishnamurti 《Meteorology and Atmospheric Physics》2007,98(3-4):137-174

Summary Climate variations in the Caribbean, largely manifest in rainfall activity, have important consequences for the large-scale water budget, natural vegetation, and land use in the region. The wet and dry seasons will be defined, and the important roles played by the El Ni?o-Southern Oscillation (ENSO) and the North Atlantic Oscillation (NAO) in modulating the rainfall during these seasons will be discussed. The seasonal climate forecasts in this paper are made by 13 state of the art coupled atmosphere-ocean general circulation models (CGCMs) and by the Florida State University Synthetic Superensemble (FSUSSE), whose forecasts are obtained by a weighted combination of the individual CGCM forecasts based on a training period. The success of the models in simulating the observed 1989–2001 climatology of the various forecast parameters will be examined and linked to the models’ success in predicting the seasonal climate for individual years. Seasonal forecasts will be examined for precipitation, sea-surface temperature (SST), 2-meter air temperature, and 850 hPa u- and v-wind components during the period 1989–2001. Evaluation metrics include root mean square (RMS) error and Brier skill score. It will be shown that the FSUSSE is superior to the individual CGCMs and their ensemble mean both in simulating the 1989–2001 climatology for the various parameters and in predicting the seasonal climate of the various parameters for individual years. The seasonal climate forecasts of the FSUSSE and of the ensemble mean of the 13 state of the art CGCMs will be evaluated for years (during the period 1989–2001) that have particular ENSO and NAO signals that are known to influence Caribbean weather, particularly the rainfall. It will be shown that the FSUSSE provides superior forecasts of rainfall, SST, 2-meter air temperature, and 850 hPa u- and v-wind components during dry summers that are modulated by negative SOI and/or positive NAO indices. Such summers have become a feature of a twenty-year pattern of drought in the Caribbean region. The results presented in this paper will show that the FSUSSE is a valuable tool for forecasting rainfall and other atmospheric and oceanic variables during such periods of drought.  相似文献