A reassessment of the economic effects of global climate change on U.S. agriculture     

Richard M. Adams  Ronald A. Fleming  Ching-Chang Chang  Bruce A. McCarl  Cynthia Rosenzweig 《Climatic change》1995,30(2):147-167

This study uses recent GCM forecasts, improved plant science and water supply data and refined economic modeling capabilities to reassess the economic consequences of long-term climate change on U.S. agriculture. Changes in crop yields, crop water demand and irrigation water arising from climate change result in changes in economic welfare. Economic consequences of the three GCM scenarios are mixed; GISS and GFDL-QFlux result in aggregate economic gains, UKMO implies losses. As in previous studies, the yield enhancing effects of atmospheric CO₂ are an important determinant of potential economic consequences. Inclusion of changes in world food production and associated export changes generally have a positive affect on U.S. agriculture. As with previous studies, the magnitude of economic effects estimated here are a small percentage of U.S. agricultural value.  相似文献   

Use of Electric Logs to Estimate Water Quality of Pre-Tertiary Aquifers     

J. B. Lindner-Lunsford  Breton W. Bruce 《Ground water》1995,33(4):547-555

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Developing A National Drinking Water Regulation for Disinfection of Ground Water     

Bruce A. Macler 《Ground Water Monitoring & Remediation》1995,15(4):77-84

The Safe Drinking Water Act directs EPA to promulgate requirements for disinfection of ground water-based drinking water systems. The Ground- water Disinfection Rule regulatory workgroup, made up of representatives from EPA, the states, and other interested parties, is actively considering the issues for the wide range of elements necessary to ensure a regulation that will protect public health and can be feasibly implemented. This regulation is likely to require disinfection of ground water sources and systems found to be contaminated or vulnerable to contamination.  相似文献   

Book reviews     

Robert Maples  Bruce W. Nelson  Peter G. Verity 《Estuaries and Coasts》1987,10(2):177-179

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SPECTROPHOTOMETRIC DETERMINATION OF FERROUS IRON IN EIGHTEEN UNITED STATES GEOCHEMICAL REFERENCE STANDARDS     

Charles B. Bruce  Jr.  Nathan W. Bower 《Geostandards and Geoanalytical Research》1987,11(1):41-42

Iron (II) oxide in 50 mg samples of silicate rocks, deposits, and soils is measured after digestion with HF and HCl in the presence of ICl. The iodine produced is measured spectrophotometrically. Results are presented for the eighteen available USGS geochemical reference standards including the GXR series.  相似文献   

Diffusion of dissolved carbonate in magmas: Experimental results and applications     

E. Bruce Watson  Mark A. Sneeringer  Alan Ross 《Earth and Planetary Science Letters》1982,61(2):346-358

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Nd isotopic characteristics of S- and I-type granites   总被引：1，自引：0，他引：1  

Malcolm T. McCulloch  Bruce W. Chappell 《Earth and Planetary Science Letters》1982,58(1):51-64

The initial Nd and Sr isotopic composition has been determined in S- and I-type granites from the Paleozoic Berridale and Kosciusko Batholiths of southeast Australia. The Nd and Sr isotopic variations form a strongly covariant array with S-types granites having a relatively restricted range inε_Nd values from ?6.1 to ?9.8 but a large range in initial⁸⁷Sr⁸⁶Sr of from 0.7094 to 0.7184. These characteristics are indicative of an～1400-m.y. sedimentary or metasedimentary source for S-types. I-types have variable initial Nd ranging from +0.4 to ?8.9, and a more limited range in initial⁸⁷Sr⁸⁶Sr of from 0.70453 to 0.7119. These isotopic characteristics are consistent with a two-component mixing model whereby a depleted mantle-like component (DMC) withε_Nd = +6 and⁸⁷Sr⁸⁶Sr= 0.703, is mixed with a crustal component (CC) havingε_Nd = ?9 and⁸⁷Sr⁸⁶Sr= 0.720. Although this two-component mixing model satisfies the isotopic constraints the source rock chemistry of the I-types is not compatible with the large proportion (up to 50%) of sedimentary material implied by the isotopic data. This indicates that more than two components are required to account for both the isotopic and chemical data. Both the chemical and isotopic data are consistent with I-type granites having been formed from source rocks of predominantly mantle derivation and obtained progressively from the mantle over a period of 1000 m.y. prior to granite formation.  相似文献   

Assessment of OCSEAP     

Herb Bruce 《Marine pollution bulletin》1982,13(6):213-214

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Long-term effects of crude oil on microbial processes in subarctic marine sediments: Studies on sediments amended with organic nutrients     

Robert P. Griffiths  Bruce A. Caldwell  William A. Broich  Richard Y. Morita 《Marine pollution bulletin》1982,13(8):273-278

Subarctic marine sediments amended with various organic compounds were exposed to fresh Cook Inlet crude oil at a concentration of 50 ppt for either 6 or 8 months. After the sediments were initially treated, they were returned to the approximate location where they were collected and left to be exposed to natural environmental conditions until they were retrieved for analysis. As a result of crude oil treatment, the activities of the enzymes that hydrolyse structural polysaccharides were reduced and the activities of the enzymes that hydrolyse storage polysaccharides were stimulated. In addition to these changes, we observed changes in phosphatase activity, nitrogen fixation rates, potential denitrification rates, methane concentrations, CO₂ production rates, and the glucose uptake and mineralization rates. The effect of the crude oil perturbation was different depending on the organic compound used in the amended sediments. Many of these differences could be explained by the effect of crude oil on the hydrolases which were responsible for degrading the compound in question. The results of this study suggest the effect of crude oil on microbial processes may be affected by the type of organic material present in the impacted marine sediment. This study also illustrates the value of measuring hydrolase activity in studies designed to determine the effects of this or any other pollutant on microbial processes in marine sediments.  相似文献   

Basalt contamination by continental crust: Some experiments and models   总被引：1，自引：1，他引：1  

E. Bruce Watson 《Contributions to Mineralogy and Petrology》1982,80(1):73-87

Chemical interaction between molten basalt and felsic minerals of the continental crust (quartz, K-feldspar, and oligoclase) was examined in static and dynamic experiments at 1,200°–1,400° C. Under circumstances of continuous stirring at 1,400°, -quartz dissolves in tholeiite melt at a rate of 3.3×10^–6 g/s per cm² of contact area; at 1,300°, the solution rate is 1.5×10^–6 g/cm{cm2}s. The feldspars are molten at the experimental conditions, and interact with contacting basalt melt by diffusion in the liquid state. This is a complex process characterized by rapid initial diffusion of alkalies to establish a distribution between felsic melt and basalt similar to that observed in cases of actual two-liquid equilibrium (both alkalies reach concentrations in the felsic melt 1.5–3 times those in the basalt). Alkali diffusion may be uphill or downhill, depending on which direction of net flux is required to produce a two-liquid type distribution. Once this distribution is attained, subsequent diffusion of all melt species is slow and apparently limited by the diffusivity of SiO₂, which is 10^–9-l0^–10 cm²/s at 1,200° C. Interdiffusion experiments involving molten basalt and synthetic granite confirm the behavior illustrated by the feldspar/basalt results, and give similar SiO₂ diffusivities.The solution rates and interdiffusion data can be used to model basalt contamination processes likely to occur in the continental crust. For the restricted case of solid quartzitic xenoliths, the uptake of SiO₂ in a well-mixed basalt magma is quite fast: appreciable SiO₂ contamination may occur over exposure times of only days to years. If basalt magma induces local melting of crustal rocks, the assimilation process becomes one of liquid-state interdiffusion. In this case, the varying diffusivities of ions and their differing preferences for silicic relative to basaltic melts can produce marked selective contamination effects. Selective contamination of ascending basaltic magmas is particularly likely in the case of K₂O, which may be introduced in substantial amounts even when other elements remain unaffected. The Na₂O content of mantle-derived magmas is buffered against contamination by crustal materials, and K₂O is buffered against further increases once it reaches a level of 1–1.5 wt.%.  相似文献