Organo-sulfur compounds in sediments of the Puget Sound basin     

Timothy S. Bates  Roy Carpenter 《Geochimica et cosmochimica acta》1979,43(8):1209-1221

Sediment samples from a variety of different environments were analyzed for organo-sulfur compounds (OSC) to provide the first characterization of the amounts and types of these compounds in sediments of the greater Puget Sound basin. A gas Chromatograph equipped with a sulfur specific flame photometric detector was used to quantify individual OSC. Compositions of OSC mixtures were essentially constant throughout the study area. Dibenzothiophene (DBT), its alkylated homologs, and an unknown compound were the predominant OSC in most samples. Concentrations of total OSC and DBT ranged from 4 to 60 and 0.4 to 2 μg/g organic carbon, respectively. The flux of OSC to the sediments at a station in central Puget Sound west of Seattle was approximately 140 ng/cm²/yr. The profile of total OSC concentration with depth showed three organic sulfur compounds that are apparently created in situ in the vicinity of where hydrogen sulfide production begins. The concentrations of the aromatic OSC were relatively constant with depth. Although several anthropogenic sources of OSC were identified, there was no evidence that OSC from these sources were accumulating in the sediments. The major source of the aromatic OSC in the sediments is apparently atmospheric input from natural sources such as forest fires.  相似文献   

Exploitation of the Gauribidanur array for seismic monitoring     

T.G. Varghese  F. Roy  B.S.S. Rao  M.P. Suryavanshi  R.N. Bharthur 《Physics of the Earth and Planetary Interiors》1979,18(2):87-94

The medium-aperture array at Gauribidanur is in continous operation since 1966. With the recent addition of a 12-bit 16-K computer its potential for the monitoring of underground explosions has improved considerably. The salient aspects of the monitoring system, the present and projected procedures for generation and dissemination of detection data and the long-term storage of data relevant to discrimination research are discussed. An attempt is also made to assess its detection efficiency in the light of the major features of site noise.  相似文献   

The early diagenesis of aliphatic hydrocarbons and organic matter in sedimentary particulates from Dabob Bay,Washington     

Fredrick G. Prahl  Joseph T Bennett  Roy Carpenter 《Geochimica et cosmochimica acta》1980,44(12):1967-1976

Aliphatic hydrocarbon compositions were quantitatively characterized in plankton, sediment trap-collected particulate materials and sediments from Dabob Bay using high resolution glass capillary gas chromatography. The average net accumulation of individual hydrocarbons measured in a 1-yr series of sediment traps was compared with the net accumulation of corresponding compounds measured in three depth intervals of ²¹⁰Pb-dated bottom sediments. Systematic and rapid decreases in the net accumulation of individual hydrocarbons were observed from the sediment traps to the sediments. Most pronounced decreases were measured for planktonically derived hydrocarbon constituents (e.g. pristane and two unsaturated compounds) which are rapidly remineralized at or near the sediment-water interface. Consequently, the amount of each compound measured in deposited sediments is not necessarily a quantitative indication of its initial flux to the sediments. The n-alkanes (C_25,27,29,31). characteristic of terrestrial plant waxes, are the predominant hydrocarbons measured by 4–6 cm depth in these sediments and show reasonably constant net accumulation below this interval.Significant diagenetic alteration of the bulk organic matter contained in the average sediment trap particulate material is also noted through comparison with bottom sediments on the basis of organic C/N and δ¹³C measurements. Organic matter elementally similar to marine plankton is preferentially remineralized upon deposition of the sedimentary particulates. The residual organic matter remaining and buried in the bottom sediments closely resembles terrestrial organic matter.  相似文献   

Measurements of Reaction Coefficients of NO2 and HONO on Aerosol Particles     

Roy M. Harrison  Gareth M. Collins 《Journal of Atmospheric Chemistry》1998,30(3):397-406

The reaction coefficients of nitrogen dioxide and nitrous acid with monodisperse sodium chloride and ammonium sulphate aerosols have been measured in a flow reactor at atmospheric pressure. These experiments were performed at relative humidities above and below the deliquescence points of both aerosols (r.h. 50 and 85%) at 279 K. The results for NO₂ afford a reaction coefficient in the range (2.8–10) × 10^-4 and for HONO, (2.8–4.6) × 10^-3. For both species, there appears to be an enhancement of the reaction coefficient on sodium chloride aerosol at 50% r.h. The results are compared with reaction coefficients determined by other experimental methods. A good agreement is found for both gases between this method and the coated denuder method previously developed in our research laboratories (Msibi et al., 1993) and with the majority of other published data for NO₂. In the case of HONO, our estimate of reaction coefficient is smaller than, or at the lower limits of the ranges reported by other published studies.  相似文献   

Problems in determining paleointensities from very old rocks     

J.L. Roy 《Physics of the Earth and Planetary Interiors》1977,13(4):319-324

Polyphase magnetizations are not uncommon in old rocks. To obtain reliable paleointensities, these magnetizations need to be recognized and separated so that the paleointensity determination can be derived from one of the phases of magnetization. Some of the techniques used to detect and separate (and sometimes isolate) the different phases are described by means of a few examples. Special attention is given to the chemical remanent magnetization which can be found in both sedimentary and igneous rocks. It appears that a sedimentary rock near an igneous contact is the preferferred specimen for reliable paleointensity determinations.  相似文献   

Distribution of gold and rhenium between nickel-iron and silicate melts: implications for the abundance of siderophile elements on the Earth and Moon     

Kan Kimura  Roy S Lewis  Edward Anders 《Geochimica et cosmochimica acta》1974,38(5):683-701

The distribution equilibrium of Au and Re between nickel-iron and basaltic melts was studied at 1400–1600°C, using radioactive tracers. Metal/silicate distribution coefficients were 1–3 orders of magnitude higher than earlier estimates, as follows. Mauna Loa basalt—Fe₁₀Ni₉₀: D_Au = 3.3 × 10⁴, D_Re = (2.4?89) × 10⁴. Gorda Ridge basalt—Fe₁₀Ni₉₀: D_Au = (18?75) × 10⁴. Synthetic lunar basalt—Fe₇₀ Ni₃₀: D_Au≥ 2 × 10⁴, D_Re ≥ 2 × 10³. The experimental ΔG₁₈₀₀^° for the distribution of Au between nickel-iron and Mauna Loa basalt is ?40 kcal/mole, compared to a calculated value of about ?110 kcal/mole for a reaction involving simple Au³⁺ ions. Presumably the difference represents stabilization of Au(III) by complex formation with ligands such as Cl^?, H₂O, etc.Gold abundances in lunar basalts are roughly consistent with the measured D_Au, but those in terrestrial basalts are two orders of magnitude too high. This discrepancy may reflect complexing by volatiles in the Earth's upper lithosphere, as well as oxidative destruction of metal in the final stages of accretion. In the absence of a metal phase, siderophile trace elements would remain trapped in the upper mantle and crust.  相似文献   

Oblique propagation of ion acoustic shock waves in weakly and highly relativistic plasmas with nonthermal electrons and positrons     

M. G. Hafez  N. C. Roy  M. R. Talukder  M. Hossain Ali 《Astrophysics and Space Science》2016,361(9):312

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Insights on the events surrounding the final drainage of Lake Ojibway based on James Bay stratigraphic sequences     

M. Roy  F. Dell’Oste  J.J. Veillette  A. de Vernal  J.-F. Hélie  M. Parent 《Quaternary Science Reviews》2011,30(5-6):682-692

Deglaciation of the James Bay region was highly dynamic, with the occurrence of ice (Cochrane) readvances into glacial Lake Ojibway around final deglaciation time, which culminated with the drainage of Ojibway waters into Hudson Bay and subsequent incursion of the Tyrrell Sea at ～8 ka. Renewed interest on these events comes from the possible link between the drainage of the ice-dammed Lake Agassiz-Ojibway and a major climate deterioration known as the 8.2-ka cooling event. Recent glaciological modeling suggests that this drainage may have occurred subglacially, a mechanism that can accommodate more than one lake discharge, as suggested by marine records. The exact number and timing of drainage events, as well as location of the lake discharge pathway(s) remain, however, largely unconstrained. Here we focus on the events that led to the drainage of Lake Ojibway by documenting late-glacial sedimentary sequences located east of James Bay. Our investigations indicate that the deglacial sequence consists of a readvance till, extensive Ojibway rhythmites, and thick marine sediments. The glaciolacustrine and marine units are separated by a 60 cm-thick horizon composed of laminated silt beds containing rounded clay balls and disseminated clasts resulting from the abrupt drainage of the lake. Radiocarbon dating of marine fossils lying above the drainage horizon indicates that the glaciolacustrine episode ended around 8128–8282 cal yr BP. Micropaleontological analyses reveal that freshwater ostracods (Candona sp.) and marine microfossils (foraminifers, dinocysts) occur together in the upper part of the Ojibway sediments. Analysis of oxygen isotopes (δ¹⁸O) of ostracods and foraminifers originating from the same stratigraphic position show highly contrasting values that suggest possible subglacial exchanges between Lake Ojibway and Tyrrell Sea waters prior to the final drainage event. The complexity of the deglacial events is further indicated by radiocarbon dating of marine shells retrieved from a Cochrane till that suggests that the last ice readvance occurred almost simultaneously with the final lake discharge. These results bring additional constraints on the drainage mechanism of the coalesced Lake Agassiz-Ojibway and indicate that the James Bay region formed an important drainage pathway for meltwaters at the end of the last deglaciation.  相似文献   

Diurnal timing of warmer air under climate change affects magnitude,timing and duration of stream temperature change     

Mousa Diabat  Roy Haggerty  Steven M. Wondzell 《水文研究》2013,27(16):2367-2378

Stream temperature will be subject to changes because of atmospheric warming in the future. We investigated the effects of the diurnal timing of air temperature changes – daytime warming versus nighttime warming – on stream temperature. Using the physically based model, Heat Source, we performed a sensitivity analysis of summer stream temperatures to three diurnal air temperature distributions of +4 °C mean air temperature: i) uniform increase over the whole day, ii) warmer daytime and iii) warmer nighttime. The stream temperature model was applied to a 37‐km section of the Middle Fork John Day River in northeastern Oregon, USA. The three diurnal air temperature distributions generated 7‐day average daily maximum stream temperatures increases of approximately +1.8 °C ± 0.1 °C at the downstream end of the study section. The three air temperature distributions, with the same daily mean, generated different ranges of stream temperatures, different 7‐day average daily maximum temperatures, different durations of stream temperature changes and different average daily temperatures in most parts of the reach. The stream temperature changes were out of phase with air temperature changes, and therefore in many places, the greatest daytime increase in stream temperature was caused by nighttime warming of air temperatures. Stream temperature changes tended to be more extreme and of longer duration when driven by air temperatures concentrated in either daytime or nighttime instead of uniformly distributed across the diurnal cycle. Copyright © 2012 John Wiley & Sons, Ltd.  相似文献   

Preliminary comparison of trace metals in coastal aerosols between Qingdao and Liverpool     

刘昌岭  张经 《中国海洋湖沼学报》2008,26(2):203-214

Aerosol samples were collected at two coastal suburban stations, Qingdao （China） in 1995-1996 and Liverpool （U.K.） in 1995, respectively. The samples were analyzed to determine the concentrations of trace metals （Cr, Zn, Cu, Co, Ni, Pb, V, and Cd） as well as A1, Fe and Mn. Data were examined to understand the difference of trace metals in aerosols between coastal zones downwind the developing area （near the Yellow Sea） and developed region （near the Irish Sea）. The results show that most elements at Qingdao have levels 4-5 times higher than those at Liverpool, particularly for the crust-dominated elements （e.g. Al, Fe and Mn）. Moreover, the aerosol composition at Qingdao is higher in spring than in summer, underlying the influence of westerlies and local emissions in combination, whereas seasonal change of aerosol composition is not significant at Liverpool. The enrichment factors for the crustal source elements （EFcrust） at Liverpool are much higher than those at Qingdao. The contributions from the pollutant source （Rp） for some trace metals like Cu, Pb, Zn and Cd are 〉90% at Qingdao and Liverpool, suggesting overwhelming anthropogenic contributions to these metals. The contributions from crustal source （Re） for trace metals tend to increase with higher aerosol levels and Al concentration at Qingdao, indicating a good correlation between the crust-dominated component and the air mass. At Liverpool, the Rc values for trace metals are positively correlated with Al concentrations instead of with aerosol mass, suggesting that Al in aerosols represents the crustal component even though the aerosols come from different sources.  相似文献