An Australian View     

M. L. Benson    W. G. Sims  G. Hildebrandt  H. Kenneweg 《The Photogrammetric Record》1970,6(35):446-451

There appears to be some confusion as to the behaviour of false colour film when used for photo-interpretation in forestry studies. The authors, working in Australia, call for a critical examination of the value of this film type. Their plea has prompted a statement, based on European experience, which forms the second section of the paper.  相似文献   

AUSTRALIS: A new tool for the study of isotopic systems and geochronology in mineral systems     

S. H. Sie  T. R. Niklaus  D. A. Sims  F. Bruhn  G. Suter  G. Cripps 《Australian Journal of Earth Sciences》2013,60(4):601-611

AUSTRALIS (AMS for Ultra Sensitive TRAce eLement and Isotopic Studies) is a microbeam accelerator mass spectrometry (AMS) system designed for in situ microanalysis of geological samples for trace elements and radiogenic and stable isotope data. The AMS method eliminates molecular and isobaric interferences in in situ mass spectrometric measurements, opening up new opportunities in geochronology and tracer applications. Tests have been carried out for measurements of Pb, S and Os isotopes, conducted mainly at 1.5 MV accelerating voltage. In Pb and S tests, precision as high as 0.3‰ has been obtained, made possible by a fast isotope switching system to counter the effect of instabilities in the ion source and beam transport system. In trace‐element analysis, a detection limit for Au at the sub‐ppb level was obtained.  相似文献   

What makes technological transfer successful?     

Kelly Sims Gallagher 《Climate Policy》2015,15(1):180-182

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Area Calculation by Electronic Printer     

W. G. Sims. 《The Photogrammetric Record》1958,2(12):453-454

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Correlation of Alaskan varve thickness with climatic parameters, and use in paleoclimatic reconstruction     

James A. Perkins  John D. Sims 《Quaternary Research》1983,20(3):308-321

The thickness of varves in the sediments of Skilak Lake, Alaska, are correlated with the mean annual temperature (r = 0.574), inversely correlated with the mean annual cumulative snowfall (r = −0.794), and not correlated with the mean annual precipitation (r = 0.202) of the southern Alaska climatological division for the years 1907–1934 A.D. Varve thickness in Skilak Lake is sensitive to annual temperature and snowfall because Skilak Glacier, the dominant source of sediment for Skilak Lake, is sensitive to these climatic parameters. Trends of varve thickness are well correlated with trends of mean annual cumulative snowfall ( ) of the southern Alaska climatological division and with trends of mean annual temperature of the southern ( ) and northern ( ) Alaska climatological divisions. Trends of varve thickness also correlate with trends of annual temperature in Seattle and North Head, Washington ( , respectively). Comparisons of trends of varve thickness with trends of annual temperature in California, Oregon, and Washington suggest no widespread regional correlation. Trends of annual snowfall in the southern Alaska climatological division and trends of annual temperature in the southern and northern Alaska climatological divisions are reconstructed for the years 1700–1906 A.D. Climatic reconstructions on the basis of varve thickness in Skilak Lake utilize equations derived from the regression of series of smoothed climatological data on series of smoothed varve thickness. Reconstruction of trends of mean annual cunulative snowfall in the southern Alaska climatological division suggests that snowfall during the 1700s and 1800s was much greater than that during the early and mid-1900s. The periods 1770–1790 and 1890–1906 show marked decreases in the mean annual snowfall. Reconstructed trends of the annual temperature of the northern and southern Alaska climatological divisions suggest that annual temperatures during the 1700s and 1800s were lower than those of the early and mid-1900s. Two periods of relatively high annual temperatures coincide with the periods of low annual snowfall thus determined.  相似文献   

Solid-state astrochemistry in star-forming regions     

Helen Fraser  David Williams  Ian Sims  Anita Richards  Jeremy Yates 《Astronomy& Geophysics》2003,44(4):4.29-4.33

Surface-catalysed chemical reactions, the molecules they form, and the implications for star formation were key themes in an international workshop on "Solid-state chemistry in star-forming regions" at the Lorentz Centre, Leiden University, the Netherlands from 14–17 April 2003. Helen Fraser, David Williams, Ian Sims, Anita Richards and Jeremy Yates report.  相似文献   

Chemical and isotopic constraints on the generation and transport of magma beneath the East Pacific Rise   总被引：2，自引：0，他引：2  

K.W.W Sims  S.J Goldstein  J Blichert-toftM.R Perfit  P KelemenD.J Fornari  P MichaelM.T Murrell  S.R HartD.J DePaolo  G LayneL Ball  M JullJ Bender 《Geochimica et cosmochimica acta》2002,66(19):3481-3504

Interpretation of U-series disequilibria in midocean ridge basalts is highly dependent on the bulk partition coefficients for U and Th and therefore the mineralogy of the mantle source. Distinguishing between the effect of melting processes and variable source compositions on measured disequilibria (²³⁸U-²³⁰Th-²²⁶Ra and ²³⁵U-²³¹Pa) requires measurement of the radiogenic isotopes Hf, Nd, Sr, and Pb. Here, we report measurements of ²³⁸U-²³⁰Th-²²⁶Ra and ²³⁵U-²³¹Pa disequilibria; Hf, Nd, Sr, and Pb isotopic; and major and trace element compositions for a suite of 20 young midocean ridge basalts from the East Pacific Rise axis between 9°28′ and 9°52′N. All of the samples were collected within the axial summit trough using the submersible Alvin. The geological setting and observational data collected during sampling operations indicate that all the rocks are likely to have been erupted from 1991 to 1992 or within a few decades of that time. In these samples, ²³⁰Th excesses and ²²⁶Ra excesses are variable and inversely correlated. Because the eruption ages of the samples are much less than the half-life of ²²⁶Ra, this inverse correlation between ²³⁰Th and ²²⁶Ra excesses can be considered a primary feature of these lavas. For the lava suite analyzed in this study, ²²⁶Ra and ²³⁰Th excesses also vary with lava composition: ²²⁶Ra excesses are negatively correlated with Na₈ and La/Yb and positively correlated with Mg#. Conversely, ²³⁰Th excesses are positively correlated with Na₈ and La/Yb and negatively correlated with Mg#. Th/U, ²³⁰Th/²³²Th, and ²³⁰Th excesses are also variable and correlated to one another. ²³¹Pa excesses are large but relatively constant and independent of Mg#, La/Yb, Th/U, and Na₈. The isotope ratios ¹⁴³Nd/¹⁴⁴Nd, ¹⁷⁶Hf/¹⁷⁷Hf, ⁸⁷Sr/⁸⁶Sr, and ²⁰⁸Pb/²⁰⁶Pb are constant within analytical uncertainty, indicating that they were derived from a common source. The source is homogeneous with respect to parent/daughter ratios Lu/Hf, Sm/Nd, Rb/Sr, and Th/U; therefore, the measured variations of Th/U, ²³⁰Th, and ²²⁶Ra excesses and major and trace element compositions in these samples are best explained by polybaric melting of a homogeneous source, not by mixing of compositionally distinct sources.  相似文献   

An Inter-Laboratory Assessment of the Thorium Isotopic Composition of Synthetic and Rock Reference Materials   总被引：2，自引：0，他引：2  

Kenneth W.W. Sims  James B. Gill  Anthony Dosseto  Dirk L. Hoffmann  Craig C. Lundstrom  Ross W. Williams  Lary Ball  Darren Tollstrup  Simon Turner  Julie Prytulak  Justin J.G. Glessner  J.J. Standish  Tim Elliott 《Geostandards and Geoanalytical Research》2008,32(1):65-91

We present a concerted international effort to cross-calibrate five synthetic Th isotope reference materials (UCSC Th "A", OU Th "U", WUN, IRMM-35 and IRMM-36), and six rock reference materials (UCSC TML, Icelandic ATHO, USGS BCR-2, USGS W-2, USGS BHVO-2, LV18) using multi-collector inductively coupled plasma-mass spectrometry (MC-ICP-MS). We then compare our new values with a compilation of literature mass spectrometric data for these reference materials and derive recommended "consensus"²³⁰Th/²³²Th values for each. We also present isotope dilution U and Th concentration data for four rock reference materials (UCSC TML, Icelandic ATHO, USGS BCR-2, USGS W-2).  相似文献   

Sequential Separation of Uranium,Hafnium and Neodymium from Natural Waters Concentrated by Iron Coprecipitation          下载免费PDF全文

Carli A. Arendt  Sarah M. Aciego  Kenneth W.W. Sims  Mark Robbins 《Geostandards and Geoanalytical Research》2015,39(3):293-303

A new ion exchange chromatography method is presented for the isolation of high field‐strength elements (HFSE) from freshwater and seawater samples that have undergone iron coprecipitation. Large volumes of water can be condensed through the application of iron coprecipitation, but clean separation of elements from the precipitate proves difficult. The technique described is a five‐column process designed to separate the HFSE, including rare earth elements such as neodymium and hafnium, before removing the iron and isolating uranium. Subsequent isolation of Nd and Hf was achieved using established ion exchange chromatography methods. The efficacy of our chemistry was verified by measurements of analytical reference materials – both reference solutions and seawater samples – subjected to the chemical separation methods described. Elution results indicate high yields (> 90%) determined by concentration measurements of a known reference material added to each column. Measurement results for isotopic compositions of seawater (U, Nd) and reference solutions (NIST SRM 960, U) were identical within uncertainty to previously published values. Compositions were identical between solutions (Spex CLMS3, Spex PLND2) that underwent different iron coprecipitation procedures. Isotopic determinations for reference materials JNdi‐1 and NIST SRM 960 measured with the mass spectrometers used in this study were in agreement with universally accepted values for these materials, and indicate high precision.  相似文献   

The effect of unevenly distributed catches on stock-size estimates using Virtual Population Analysis (Cohort Analysis)   总被引：1，自引：0，他引：1  

Sims  S. E. 《ICES Journal of Marine Science》1982,40(1):47-52

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