Tidal river sediments in the Washington,D.C. area. III. Biological effects associated with sediment contamination     

Christian E. Schlekat  Beth L. McGee  Eli Reinharz  David J. Velinsky  Terry L. Wade 《Estuaries and Coasts》1994,17(2):334-344

Sediment toxicity and benthic macroinvertebrate community structure were measured as one component of a study cohceived to determine the distribution and effect of sediment contamination in tidal freshwater portions of the Potomac and Anacostia rivers in the Washington, D.C., area. Samples were collected at 15 sites. Analyses included a partial life cycle (28 d) whole sediment test using the amphipod Hyalella azteca (Talitridae) and an assessment of benthic community structure. Survival and growth (as estimated by amphipod length) were experimental endopoints for the toxicity test. Significant mortality was observed in 5 of 10 sites in the lower Anacostia River basin and at the main channel Potomac River site. Sublethal toxicity, as measured by inhibition of amphipod growth, was not observed. Toxicity test results were in general agreement with synoptically measured sediment contaminant concentrations. Porewater total ammonia (NH₃+NH₄ ⁺) appears to be responsible for the toxicity of sediments from the Potomac River, while correlation analysis and simultaneously extracted metals: acid volatile sulfide (SEM∶AVS) results suggest that the toxicity associated with Anacostia River sediments was due to organic compounds. Twenty-eight macroinvertebrate taxa were identified among all sites, with richness varying from 5 to 17 taxa per site. Groups of benthic assemblages identified by group-average cluster analysis exhibited variable agreement with sediment chemical and sediment toxicity results. Integration of toxicological, chemical, and ecological components suggests that adverse environmental effects manifest in the lower Anacostia River benthos result from chemical contamination of sediment.  相似文献   

Climatic change and the Mediterranean: edited by L. Jeftic, J.D. Milliman and G. Stetini Edward Arnold, London, 1993, 672 pp, £89.50     

Paula A. Harrison 《Global Environmental Change》1993,3(4)

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Focal mechanisms of large earthquakes in the South Island of New Zealand: implications for the accommodation of Pacific-Australia plate motion     

Helen Anderson  Terry Webb  James Jackson 《Geophysical Journal International》1993,115(3):1032-1054

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Assessing Pesticide Contamination to Ground Water: A Rapid Approach   总被引：1，自引：0，他引：1  

Majid Ehteshami  Richard C. Peralta  Hubert Eisele  Howard Deer  Terry Tindall 《Ground water》1991,29(6):862-868

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The structure, mass and interactions of the hydrothermal plumes at 26°N on the Mid-Atlantic Ridge     

Terry A. Nelsen  Evan B. Forde 《Earth and Planetary Science Letters》1991,106(1-4)

Water-column surveys by combined nephelometer/CTD (NCTD) tows contributed to the 1985 discovery of the first black smokers on the Mid-Atlantic Ridge. Subsequent regional water-column mapping has helped define the extent, mass and interactions of the suspended particulate matter phase (SPM) of the hydrothermal plumes emanating from the known and other nearby sources. The results of 29 NCTD cast/tows, covering 25–30 km² of ridge segment, indicate the presence of as many as two additional sources based on SPM concentration gradients and plume-top doming over source areas. Plume doming, documented here for the first time from field observations, conforms strikingly with laboratory experiments and can serve as a marker for source field location. A comparison of the plumes' SPM with potential temperature and salinity distributions indicates close correlation in water-column anomaly patterns for each, confirming modification of the regional potential temperature and salinity structure by hydrothermal plumes, which is expressed by wide separation and sloping of isotherms and isohalines.  相似文献   

The role of salt in fold-and-thrust belts     

Dan M. Davis  Terry Engelder 《Tectonophysics》1985,119(1-4)

The style of deformation in thin-skinned fold-and-thrust belts is critically dependent upon the resistance to sliding along the detachment between the mass of deforming sediments and the underlying rocks. Evaporites can provide an extremely weak horizon within which a basal detachment can form and along which only a relatively small shear traction can be supported. Fold-and-thrust belts that form atop a salt layer, such as the Appalachian Plateau, the Franklin Mountains in northwestern Canada, and the Jura of the Alps, among others, share several readily observable characteristics. As predicted by a simple mechanical model for fold-and-thrust belts, a detachment in salt permits a thrust belt to have an extremely narrow cross-sectional taper. In addition, predicted orientations of the principal stress axes over a salt décollement are consistent with the commonly observed lack of a consistently dominant vergence direction of structures within the thrust belt. Other common attributes of salt-basal thin-skinned deformation include the presence of several widely but regularly spaced folds and abrupt changes in deformational style at the edge of the salt basin.  相似文献   

The behavior of apatite during crustal anatexis: Equilibrium and kinetic considerations   总被引：5，自引：0，他引：5  

T.Mark Harrison  E.Bruce Watson 《Geochimica et cosmochimica acta》1984,48(7):1467-1477

The solubility and dissolution kinetics of apatite in felsic melts at 850°–1500°C have been examined experimentally by allowing apatite crystals to partially dissolve into apatite-undersaturated melts containing 0–10 wt% water. Analysis of P and Ca gradients in the crystal/melt interfacial region enables determination of both the diffusivities and the saturation levels of these components in the melt. Phosphorus diffusion was identified as the rate-limiting factor in apatite dissolution. Results of four experiments at 8 kbar run in the virtual absence of water yield an activation energy (E) for P diffusion of 143.6 ± 2.8 kcal-mol^?1 and frequency factor (D₀) of 2.23^+2.88_?1.26 × 10⁹cm²-sec^?1. The addition of water causes dramatic and systematic reduction of both E and D₀ such that at 6 wt% H₂O the values are ~25 kcal-mol^?1 and 10^?5 cm²-sec^?1, respectively. At 1300°C, the diffusivity of P increases by a factor of 50 over the first 2% of water added to the melt, but rises by a factor of only two between 2 and 6%, perhaps reflecting the effect of a concentration-dependent mechanism of H₂O solution. Calcium diffusion gradients do not conform well to simple diffusion theory because the release of calcium at the dissolving crystal surface is linked to the transport rate of phosphorus in the melt, which is typically two orders of magnitude slower than Ca. Calcium chemical diffusion rates calculated from the observed gradients are about 50 times slower than calcium tracer diffusion.Apatite solubilities obtained from these experiments, together with previous results, can be described as a function of absolute temperature (T) and melt composition by the expression: In D^apatite/melt_P = [(8400 + ((SiO₂ ? 0.5)2.64 × 10⁴))/T] ? [3.1 + (12.4(SiO₂ ? 0.5))] where SiO₂ is the weight fraction of silica in the melt. This model appears to be valid between 45% and 75% SiO₂, 0 and 10% water, and for the range of pressures expected in the crust.The diffusivity information extracted from the experiments can be directly applied to several problems of geochemical interest, including I) dissolution times for apatite during crustal anatexis, and 2) pileup of P, and consequent local saturation in apatite, at the surfaces of growing major-mineral phases.  相似文献   

The stability and behavior of a frictional system with a two state variable constitutive law     

Michael L. Blanpied  Terry E. Tullis 《Pure and Applied Geophysics》1986,124(3):415-444

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Zircon saturation revisited: temperature and composition effects in a variety of crustal magma types   总被引：38，自引：0，他引：38  

E. Bruce Watson  T. Mark Harrison 《Earth and Planetary Science Letters》1983,64(2):295-304

Hydrothermal experiments in the temperature range 750–1020°C have defined the saturation behavior of zircon in crustal anatectic melts as a function of both temperature and composition. The results provide a model of zircon solubility given by: In D_Zr^zircon/melt= ?3.80?[0.85(M?1)]+12900/T where D_Zr^zircon/melt is the concentration ratio of Zr in the stoichiometric zircon to that in the melt, T is the absolute temperature, and M is the cation ratio (Na + K + 2Ca)/(Al · Si). This solubility model is based principally upon experiments at 860°, 930°, and 1020°C, but has also been confirmed at temperatures up to 1500°C for M = 1.3. The lowest temperature experiments (750° and 800°C) yielded relatively imprecise, low solubilities, but the measured values (with assigned errors) are nevertheless in agreement with the predictions of the model.For M = 1.3 (a normal peraluminous granite), these results predict zircon solubilities ranging from ～ 100 ppm dissolved Zr at 750°C to 1330 ppm at 1020°C. Thus, in view of the substantial range of bulk Zr concentrations observed in crustal granitoids (～ 50–350 ppm), it is clear that anatectic magmas can show contrasting behavior toward zircon in the source rock. Those melts containing insufficient Zr for saturation in zircon during melting can have achieved that condition only by consuming all zircon in the source. On the other hand, melts with higher Zr contents (appropriate to saturation in zircon) must be regarded as incapable of dissolving additional zircon, whether it be located in the residual rocks or as crystals entrained in the departing melt fraction. This latter possibility is particularly interesting, inasmuch as the inability of a melt to consume zircon means that critical geochemical “indicators” contained in the undissolved zircon (e.g. heavy rare earths, Hf, U, Th, and radiogenic Pb) can equilibrate with the contacting melt only by solid-state diffusion, which may be slow relative to the time scale of the melting event.  相似文献   

Selective concentration of cesium in analcime during hydrothermal alteration,Yellowstone National Park,Wyoming     

Terry E.C Keith  J.M Thompson  Robert E Mays 《Geochimica et cosmochimica acta》1983,47(4):795-804

Chemical and mineralogical studies of fresh and hydrothermally altered rhyolitic material in Upper and Lower Geyser Basins, Yellowstone National Park, show that all the altered rocks are enriched in Cs and that Cs is selectively concentrated in analcime. The Cs content of unaltered rhyolite lava flows, including those from which the altered sediments are derived, ranges from 2.5 to 7.6 ppm. The Cs content of analcime-bearing altered sedimentary rocks is as high as 3000 ppm, and in clinoptilolite-bearing altered sedimentary rocks Cs content is as high as 180 ppm. Altered rhyolite lava flows which were initially vitrophyres, now contain up to 250 ppm Cs, and those which were crystallized prior to hydrothermal alteration contain up to 14 ppm. Mineral concentrates of analcime contain as much as 4700 ppm Cs. The Cs must have been incorporated into the analcime structure during crystallization, rather than by later cation substitution, because analcime does not readily exchange Cs. The $\text{Cs}\text{Cl}$ of the fluids circulating through the hydrothermal system varies, suggesting that Cs is not always a conservative ion and that Cs is lost from upflowing thermal waters due to water-rock interaction resulting in crystallization of Cs-bearing analcime.The source of Cs for Cs enrichment of the altered rocks is from leaching of rhyolitic rocks underlying the geyser basins, and from the top of the silicic magma chamber that underlies the area.Analcime is an important natural Cs sink, and the high Cs concentrations reported here may prove to be an important indicator of the environment of analcime crystallization.  相似文献