Induced stresses and fault potential in eastern Canada due to a realistic load: a preliminary analysis   总被引：1，自引：0，他引：1  

Patrick Wu  Henry S. Hasegawa 《Geophysical Journal International》1996,127(1):215-229

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The replacement of anthophyllite by jimthompsonite: a model for hydration reactions in biopyriboles     

Bernard Henry Grobéty 《Contributions to Mineralogy and Petrology》1997,127(3):237-247

Anthophyllite crystals found in ultramafic lenses of the Lepontine Alps (Switzerland) contain coherent, submicroscopic intergrowths of ordered and disordered biopyribole polysomes. The chain width distributions of disordered polysomes were analyzed using high resolution transmission electron microscopy (HRTEM). Chains wider than triple were interpreted as intermediate products in the transformation of anthophyllite to the triple chain silicate jimthompsonite. The concentration of individual chain types is strongly correlated with the reaction progress. Based on observed zipper terminations and the transformation rules given by Veblen and Buseck (1980) a scheme of possible reaction paths leading from anthophyllite to jimthomp sonite is proposed. The reaction scheme and a simple kinetic model for elementary reactions allow modeling of the observed chain width distributions. The model suggests that the complex reaction paths involving steps with increasing and decreasing chain width are more important in the formation of jimthompsonite than the direct transformation from anthophyllite. The wide chains (>triple) occurring as intermediate products of the multi-step paths are structurally closer to talc than jimthompsonite. The back-transformation of these wide chains to triple chains is, therefore, a strong argument that jimthompsonite is a stable phase and not only a metastable intermediate product in the transformation of anthophyllite to talc. Received: 8 July 1996 / Accepted: 13 December 1996  相似文献   

Submarine Ground Water Discharge and Salt Penetration Across the Sea Floor   总被引：1，自引：0，他引：1  

Henry Bokuniewicz  Meagen Pollock  John Blum  Robert Wilson 《Ground water》2004,42(7):983-989

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‘Committing to Place’ at the Local Scale: the potential of youth education programs for promoting community participation in regional natural resource management     

Ruth Lane  Damian Lucas  Frank Vanclay  Sophie Henry  Ian Coates 《The Australian geographer》2005,36(3):351-367

Emerging approaches to environmental governance require a greater level of community participation than did previous approaches in which these responsibilities largely rested with government agencies. There is consequently a need for increased engagement with NRM among a broad community sector. This paper examines initiatives by two prominent government agencies, the Murray–Darling Basin Commission (MDBC) and the National Museum of Australia (NMA), to engage school children from regional communities using education programs that focus on place and environmental health. We focus on the MDBC's International Riverhealth Conference held in Mildura in 2003 and the associated Murray–Darling Basin TalkBack Classroom sponsored by the NMA and the Parliamentary Education Office (PEO). We explore how key themes of local scale, place-based identities, youth voice and critical engagement are developed in these programs and consider how they relate to the environmental agency of children. We then reflect on the potential for the kinds of environmental agency promoted through these programs to help build the capacity of local communities to progress larger goals of environmental restoration and sustainability in the Murray–Darling Basin. The evaluation research reported here forms part of the Committing to Place research project, an Australian Research Council Linkage grant involving the University of Tasmania, the National Museum of Australia and the Murray–Darling Basin Commission.  相似文献   

Variations of U and Sr isotope ratios in Alsace and Luxembourg rain waters: origin and hydrogeochemical implications     

Franois Chabaux  Jean Riotte  Anne-Dsire Schmitt  Jean Carignan  Pierre Herckes  Marie-Claire Pierret  Henry Wortham 《Comptes Rendus Geoscience》2005,337(16):4612

Major and trace element concentrations, as well as Sr and U isotope ratios, were measured in rainwater samples collected in three different locations in Alsace (East of France) and Luxembourg: a mid-altitude mountain site (Aubure Environment HydroGeochemical Observatory), an urban site (Strasbourg) and a peri-urban site located in an area of well developed industrial activity (Esch-sur-Alzette in Luxembourg). Results highlight the quite high spatial and temporal variability of the chemical and isotopic characteristics of rainwater at the regional scale. They also suggest a quite systematic contribution of a local component in the chemical composition of rainwater. In urban and peri-urban sites, the local component is certainly linked to human activities, as it is well illustrated in this study with the Esch-sur-Alzette samples. On the other hand, for the Aubure site, i.e. a small forested watershed of mid-altitude mountain, data presented in this study demonstrate the influence of the vegetation on the chemical composition of rainwater for alkali and calc-alkali elements, as well as for the Sr isotope ratios. Such a result questions the reliability of the method classically used to estimate the rainwater contribution on the river chemical budget. In addition, data of the present study confirm the very low content of uranium in rainwater and demonstrate, especially through the U isotope analysis of Aubure rainwater, the negligible effect of rainwater on U budget of river waters. This work thus outlines the property of U to be a geochemical tracer specific of weathering fluxes carried by rivers. To cite this article: F. Chabaux et al., C. R. Geoscience 337 (2005).  相似文献   

How to increase earthquake and home fire preparedness: the fix-it intervention     

Helene Joffe  Gabriela Perez-Fuentes  Henry W. W. Potts  Tiziana Rossetto 《Natural Hazards》2016,84(3):1943-1965

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The St. Gallen Fault Zone: a long-lived,multiphase structure in the North Alpine Foreland Basin revealed by 3D seismic data     

Stefan Heuberger  Philippe Roth  Olivier Zingg  Henry Naef  Beat P. Meier 《Swiss Journal of Geoscience》2016,109(1):83-102

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The multiple chronological techniques applied to the Lake Suigetsu SG06 sediment core,central Japan     

Richard A. Staff  Takeshi Nakagawa  Gordon Schlolaut  Michael H. Marshall  Achim Brauer  Henry F. Lamb  Christopher Bronk Ramsey  Charlotte L. Bryant  Fiona Brock  Hiroyuki Kitagawa  Johannes van der Plicht  Rebecca L. Payne  Victoria C. Smith  Darren F. Mark  Alison Macleod  Simon P. E. Blockley  Jean‐Luc Schwenninger  Pavel E. Tarasov  Tsuyoshi Haraguchi  Katsuya Gotanda  Hitoshi Yonenobu  Yusuke Yokoyama  Suigetsu Project Members 《Boreas: An International Journal of Quaternary Research》2013,42(2):259-266

The varved sediment of Lake Suigetsu (central Japan) provides a valuable opportunity to obtain high‐resolution, multi‐proxy palaeoenvironmental data across the last glacial/interglacial cycle. In order to maximize the potential of this archive, a well‐constrained chronology is required. This paper outlines the multiple geochronological techniques being applied – namely varve counting, radiocarbon dating, tephrochronology (including argon–argon dating) and optically stimulated luminescence (OSL) – and the approaches by which these techniques are being integrated to form a single, coherent, robust chronology. Importantly, we also describe here the linkage of the floating Lake Suigetsu (SG06) varve chronology and the absolute (IntCal09 tree‐ring) time scale, as derived using radiocarbon data from the uppermost (non‐varved) portion of the core. This tie‐point, defined as a distinct (flood) marker horizon in SG06 (event layer B‐07–08 at 1397.4 cm composite depth), is thus derived to be 11 255 to 11 222 IntCal09 cal. years BP (68.2% probability range).  相似文献   

Acidic deposition impacts mediated by sulfur cycling in a coastal plain forest ecosystem     

Mark D. Morgan  Ralph E. Good  Henry G. Spratt Jr. Dr. 《GeoJournal》1988,17(2):183-187

Deposition in the New Jersey Pinelands was very acidic (pH=4.17) and contained high levels of SO₂ ⁻² based on bulk deposition measurementsfrom July 1984–July 1986. Streamwater over the same interval in undisturbed watersheds was less acidic (pH =4.52) and had proportionately less SO₄ ⁻². A preliminary alkalinity budget for undisturbed watersheds suggested that SO₄ ⁻² retention within Pinelands watersheds accounted for a large portion of the total alkalinity generated and thereby lessened the impact of acidic deposition on surface waters. The only process capable of explaining the retention of SO₄ ⁻² was microbial sulfate reduction in the extensive wetlands surrounding Pinelands streams which occurred at high rates.  相似文献   

The surface of labradorite feldspar after acid hydrolysis     

William H. Casey  Henry R. Westrich  Thomas Massis  Jillian F. Banfield  George W. Arnold 《Chemical Geology》1989,78(3-4):205-218

After reaction with a pH < 4, the surface of labradorite is extensively enriched in Si and H, and depleted in Al, Ca and Na relative to an unreacted crystal. However, the amount of hydrogen measured in the reacted surface is less than that predicted on the basis of exchange of hydrogen (or hydronium) ions for cations in the feldspar. By analogy with studies of silicate glass, this low concentration of hydrogen suggests that some silanol groups in the reacted surface repolymerize subsequent to ion-exchange and depolymerization reactions. The net result is a relatively porous, Si-rich leached layer which is amorphous to electron diffraction, and which allows rapid diffusion of unreactive solutes.

Both the surface area of the reacted feldspar and the porosity increase with acid hydrolysis. Modeling of nitrogen sorption onto the surface suggests that the pores have a nominal radius of 20–80 Å or less. This distribution of pore sizes resembles other acid-reacted silicate materials, such as glass, chrysotile and kaolinite. Although the mineral surface clearly becomes more porous during acid hydrolysis, the increase in powder area also does not coincide with an increase in the flux of dissolved Si from the powder. We thus attribute most of this increase in area to spallation of the silica-rich surface from the feldspar upon drying.  相似文献