Chlorinated hydrocarbons in seawater: Analytical method and levels in the northeastern Pacific     

Edward D. Scura  Vance E. McClure   《Marine Chemistry》1975,3(4):337-346

A method is described for analyzing nanogram quantities of chlorinated hydrocarbons from 1-1 samples of seawater. Seawater samples are pumped through a copper column containing a mixture by weight of 5% activated carbon powder, 10% MgO and 85% refined diatomaceous earth. The chlorinated hydrocarbons in the seawater are adsorbed or trapped on the column and subsequently eluted with 30% benzene in acetone (v/v) for analysis by gas-liquid chromatography.This procedure was used to analyze chlorinated hydrocarbon levels in samples collected off the southern California coast. We suggest that anthropogenic chlorinated hydrocarbons can be used for the investigation of large-scale ocean currents and mixing processes.  相似文献   

Multi-AUV Control and Adaptive Sampling in Monterey Bay   总被引：3，自引：0，他引：3  

Edward Fiorelli Naomi Ehrich Leonard Pradeep Bhatta Derek A. Paley Ralf Bachmayer David M. Fratantoni 《Oceanic Engineering, IEEE Journal of》2006,31(4):935-948

Operations with multiple autonomous underwater vehicles (AUVs) have a variety of underwater applications. For example, a coordinated group of vehicles with environmental sensors can perform adaptive ocean sampling at the appropriate spatial and temporal scales. We describe a methodology for cooperative control of multiple vehicles based on virtual bodies and artificial potentials (VBAP). This methodology allows for adaptable formation control and can be used for missions such as gradient climbing and feature tracking in an uncertain environment. We discuss our implementation on a fleet of autonomous underwater gliders and present results from sea trials in Monterey Bay in August, 2003. These at-sea demonstrations were performed as part of the Autonomous Ocean Sampling Network (AOSN) II project  相似文献   

A new titanium-bearing calcium aluminosilicate phase: II. Crystallography and crystal chemistry of grains formed in slowly cooled melts with bulk compositions of calcium- aluminum-rich inclusions     

David J. Barber  John R. Beckett  Julie M. Paque  Edward Stolper 《Meteoritics & planetary science》1994,29(5):682-690

Abstract The crystallography and crystal chemistry of a new calcium-titanium-aluminosilicate mineral (UNK) observed in synthetic analogs to calcium-aluminum-rich inclusions (CAIs) from carbonaceous chondrites was studied by electron diffraction techniques. The unit cell is primitive hexagonal or trigonal, with a = 0.790 ± 0.002 nm and c = 0.492 ± 0.002 nm, similar to the lattice parameters of melilite and consistent with cell dimensions for crystals in a mixer furnace slag described by Barber and Agrell (1994). The phase frequently displays an epitactic relationship in which melilite acts as the host, with (0001)_UNK | (001)_mel and <10T0>_UNK | <100>_mel. If one of the two space groups determined by Barber and Agrell (1994) for their sample of UNK is applicable (P3ml or P31m), then the structure is probably characterized by puckered sheets of octahedra and tetrahedra perpendicular to the c-axis with successive sheets coordinated by planar arrays of Ca. In this likely structure, each unit cell contains three Ca sites located in mirror planes, one octahedrally coordinated cation located along a three-fold axis and five tetrahedrally coordinated cations, three in mirrors and two along triads. The octahedron contains Ti but, because there are 1.3–1.9 cations of Ti/formula unit, some of the Ti must also be in tetrahedral coordination, an unusual but not unprecedented situation for a silicate. Tetrahedral sites in mirror planes would contain mostly Si, with lesser amounts of Al while those along the triads correspondingly contain mostly Al with subordinate Ti. The structural formula, therefore, can be expressed as with Si + Ti = 4. Compositions of meteoritic and synthetic Ti-bearing samples of the phase can be described in terms of a binary solid solution between the end-members Ca₃TiAl₂Si₃O₁₄ and Ca₃Ti(AlTi)(AlSi₂)O₁₄. A Ti-free analog with a formula of Ca₃Al₂Si₄O₁₄ synthesized by Paque et al. (1994) is thought to be related structurally but with the octahedral site being occupied by Al, that is   相似文献   

Water ice polymorphs and their significance on planetary surfaces     

Edward S. Gaffney  Dennis L. Matson 《Icarus》1980,44(2):511-519

Impacts into an icy surface could produce significant amounts of high pressure forms of water ice. Due to the relatively low ambient surface temperatures on satellites in the outer solar system and the modest temperature rises accompanying the impact pressures required for water ice metamorphism, high-pressure polymorphs will be created by and may remain after large cratering events. If so, those high-pressure ices should be ubiquitous. Low-pressure cubic ice may be abundant as well. Impacts into an icy regolith may both produce high-pressure polymorphs from ice I and destroy high-pressure polymorphs already present. The result will be an (unknown) equilibrium concentration of high pressure polymorphs in the regolith. Polymorphs may be detectable and mappable by reflection spectroscopy at vacuum ultraviolet and mid-infrared wavelengths.  相似文献   

Atmospheric water vapor flux,bifurcation of the thermohaline circulation,and climate change     

Huaxiao Wang  G Edward Birchfield 《Climate Dynamics》1992,8(1):49-53

Latitudinal heat transport in the ocean and atmosphere represents a fundamental process of the Earth's climate system. The ocean component of heat transport is effected by the thermohaline circulation. Changes in this circulation, and hence latitudinal heat transport, would have a significant effect on global climate. Paleoclimate evidence from the Greenland ice cores and deep sea sediment cores suggests that during much of glacial time the climate system oscillated between two different states. Bimodal equilibrium states of the thermohaline circulation have been demonstrated in climate models. We address the question of the role of the atmospheric hydrological cycle on the global thermohaline circulation and the feedback to the climate system through changes in the ocean's latitudinal heat transport, with a simple coupled ocean-atmosphere energy-salt balance model. Two components of the atmospheric hydrological cycle, i.e., latitudinal water vapor transport and the net flux of water vapor from the Atlantic to the Pacific Ocean appear to play separate roles. If the inter-basin transport is sufficiently large, small changes in water vapor transport over the North Atlantic can effect bifurcation or a rapid transition between two different equilibria in the global thermohaline circulation; maximum difference between the modes occurs in the North Atlantic. If the inter-basin transport is from the Pacific to the Atlantic and sufficiently large, latitudinal vapor transport in the North Pacific controls the bifurcations, with maximum changes occurring in the North Pacific. For intermediate values of inter-basin transport, no rapid transitions occur in either basin. In the regime with vapor flux from the Atlantic to the Pacific, the on mode has strong production of deep water in the North Atlantic and a large flux of heat to the atmosphere from the high latitude North Atlantic. The off mode has strong deep water production in the Southern Ocean and weak production in the North Pacific. Heat transport into the high latitude North Atlantic by the ocean is reduced to about 20% of the on mode value. For estimated values of water vapor transport for the present climate the model asserts that while water vapor transport from the Atlantic to the Pacific Ocean is sufficiently large to make the North Atlantic the dominant region for deep water production, latitudinal water vapor transport is sufficiently low that the thermohaline circulation appears stable, i.e., far from a bifurcation point. This conclusion is supported to some extent by the fact that the high latitude temperature of the atmosphere as recorded in the Greenland ice cores has changed little over the last 9000 years.  相似文献   

Spectral-compositional variations in the constituent minerals of mafic and ultramafic assemblages and remote sensing implications     

Edward A. Cloutis  Michael J. Gaffey 《Earth, Moon, and Planets》1991,53(1):11-53

The 0.3–2.6 m reflectance spectra of most mafic and ultramafic assemblages can best be interpreted by considering the spectra as being composed of mafic silicate spectra modified by the presence of opaques, such as ilmenite or magnetite, and plagioclase feldspar. The systematic spectral-compositional relationships for olivine, orthopyroxene, and clinopyroxene have been examined and it has been determined that absorption band wavelength positions are correlated with ferrous iron content. Binary mafic silicate mixtures are generally less well understood, but certain spectral features such as reflectance maxima and minima wavelength positions and absorption band areas can be used to quantify or at least constrain end member abundances and compositions. The addition of opaques to a mafic silicate assemblage lowers overall reflectance and band depths. This differs from the effects of increasing grain size which are to lower overall reflectance but increase band depths. Plagioclase is relatively transparent compared to mafic silicates and must be present in appreciable amounts (tens of percent) to be spectrally detectable. The reflectance spectra of most mafic and ultramafic assemblages are dominated by mafic silicate absorption features and analysis of their spectra on this basis allows constraints to be placed on properties such as end member abundances and compositions.  相似文献   

Noble gases in the Allende and Abee meteorites and a gas-rich mineral fraction: investigation by stepwise heating     

B. Srinivasan  Roy S. Lewis  Edward Anders 《Geochimica et cosmochimica acta》1978,42(2):183-198

Noble gases in three meteoritic samples were examined by stepwise heating, in an attempt to relate peaks in the outgassing curves to specific minerals: NeKrXe in Allende (C3V) and an Allende residue insoluble in HF-HCl, and Xe in Abee (E4). In Allende, chromite and carbon contain most of the trapped Ne (²⁰Ne/²²Ne ≈ 8.7) and anomalous Xe enriched in light and heavy isotopes, and release it at ~850°C (bulk meteorite) or 1000°C (residue). Mineral Q, containing most of the trapped Ar, Kr, Xe as well as some Ne (²⁰Ne/²²Ne ≈ 10.4), releases its gases mainly between 1200 and 1600°C, well above the release temperatures of organic polymers (300–500°) or amorphous carbon (800–1000°). The high noble-gas release temperature, ready solubility in oxidizing acids, and correlation with acid-soluble Fe and Cr all point to an inorganic rather than carbonaceous nature of Q.All the radiogenic ¹²⁹Xe is contained in HCl, HF-soluble minerals, and is distributed as follows over the peaks in the release curve: Attend 1000° (75%), 1300° (25%); Abee (data of Hohenberg and Reynolds, 1969) ~850° (15%), 1100° (60%), 1300° (25%). No conclusive identifications of host phases can yet be given; possible candidates are troilite and silicates for Allende, and djerfisherite, troilite and silicates for Abee.Mineral Q strongly absorbs air xenon, and releases some of it only at 800–1000°C. Dilution by air Xe from Q and other minerals may explain why temperature fractions from bulk meteorites often contain less ^124–130Xe for a given enrichment in heavy isotopes than does xenon from etched chromitecarbon samples, although chromite-carbon is the source of the anomalous xenon in either case. Air xenon contamination thus is an important source of error in the derivation of fission xenon spectra.  相似文献   

Primary fractionation of elements among iron meteorites     

Edward R.D. Scott 《Geochimica et cosmochimica acta》1978,42(9):1447-1458

The primary fractionation process in iron meteorites is that responsible for the distribution of elements between the groups, most notably Ga and Ge, which show concentration ranges of 10³ and 10⁴ respectively. To investigate the cause of the primary fractionation, concentrations of 16 elements were converted to relative abundances by dividing the element/Ni ratio by the CI chondrite ratio. These abundances were plotted on logarithmic graphs with data for each group (except IB and IIICD) and each cluster of closely related anomalous irons averaged.Co, P, Au, As, Cu, Sb, Ge and Zn are positively correlated with Ga. For most groups (except IA, IC and IIAB) relative abundances of these elements tend to decrease from about 1 in approximately the order listed above. This is the expected order in which these elements will condense into Fe, Ni during equilibrium nebular condensation. Mean relative abundances of refractory elements in groups generally lie within a narrow range of 0.5–2, and are uncorrelated with Ga. Although the equilibrium model may be only a gross approximation, it suggests that most primary fractionation did occur during nebular condensation.The anomalous irons are essential for defining many of the primary fractionation trends. On several element-Ga graphs the displacements of the anomalous irons from the primary curves indicate that these irons experienced the same secondary fractionation process (probably fractional crystallization) that produced the trends within most groups. The anomalous irons appear to be samples from over 50 minor groups, which have similar histories to the 12 major groups.  相似文献   

Evidence for the depletion of ammonia in the Uranus atmosphere     

Samuel Gulkis  Michael A. Janssen  Edward T. Olsen 《Icarus》1978,34(1):10-19

The theoretical disk brightness temperature spectra for Uranus are computed and compared with the observed microwave spectrum. It is shown that the emission observed at short centimeter wavelengths originates deep below the region where ammonia would ordinarily begin to condense. We demonstrate that this result is inconsistent with a wide range of atmospheric models in which the partial pressure of NH₃ is given by the vapor-pressure equation in the upper atmosphere. It is estimated that the ammonia mixing ratio must be less than 10^?6 in the 150 to 200°K temperature range. This is two orders of magnitude less than the expected mixing ratio based on solar abundances. The evidence for this depletion and a possible explanation are discussed.  相似文献   

The prominence-corona interface compared with the chromosphere-corona transition region     

Frank Q. Orrall  Edward J. Schmahl 《Solar physics》1976,50(2):365-381

The intensities of 52 EUV emission lines from each of 9 hedgerow prominences observed at the limb with the Harvard experiment on ATM-Skylab have been compared with intensities from the interior of network cells at the center of the disk, in order to compare the prominence-corona (P-C) interface with the chromosphere-corona (C-C) transition region. The intensity ratio I _cell/I _prominence for each line varies systematically (in all of the prominences observed), with the temperature of formation of the line as T ^–0.6. The density sensitive C iii (formed at T 9 × 10⁴ K) line ratio I ₁₁₇₅/I ₉₇₇ implies an average density 1.3 × 10⁹ electrons cm^–3 in the P-C interface and 4 times this value in the C-C transition of the cells. The total optical thickness at the head of the Lyman continuum is 10 in most of the prominences studied; in two of the prominences, however, we cannot reject the possibility that _o is large. Methods of analysis of these EUV data are developed assuming both a resolved and an unresolved internal prominence structure. Although the systematic differences between the P-C interface and the C-C transition are stressed, the similarities are probably more remarkable and may be a result of fine structure in the C-C transition.Currently on leave from the Institute of Astronomy, Hawaii; at the Laboratory for Atmospheric and Space Physics, University of Colorado, Boulder, Colorado, 80309.  相似文献