Oceanic Minerals: Their Origin, Nature of Their Environment, and Significance
Total Page:16
File Type:pdf, Size:1020Kb
Load more
Recommended publications
-
THE GEOCHEMICAL NEWS Quarterly Newsletter of the Geochemical Society
THE GEOCHEMICAL NEWS Quarterly Newsletter of The Geochemical Society NUMBER 101 ISSN 0016-7010 OCTOBER 1999 Life Keeps Getting Better - page 19 In this issue: Of Knights and Barons.....................................6 ISSOL ‘99 Meeting Report..............................7 Minutes of the Annual GS Board Meeting.......8 A Portrait of Sir Keith O’Nions A Portrait of Professor Sir Keith O’Nions.....10 Life Keeps Getting Better...............................19 - page 10 Astrobiology: A New Science........................22 Meetings Calendar .........................................23 Goldschmidt 2000 GS Special Publications..................................26 Oxford, U. K. GS Membership Application .........................27 September 3-8, 2000 http://www.campublic.co.uk/science/conference/Gold2000 2 The Geochemical News #101, October 1999 THE GEOCHEMICAL SOCIETY The Geochemical Society is a nonprofit scientific society founded to encourage the application of chemistry to the solution of geologi- cal and cosmological problems. Membership is international and diverse in background, encompassing such fields as organic geochem- istry, high and low-temperature geochemistry, petrology, meteorit- ics, fluid-rock interaction, and isotope geochemistry. The Society produces a Special Publications Series, The Geochemical News OFFICERS - 1999 (this quarterly newsletter), the Reviews in Mineralogy and Geochem- istry Series (jointly with the Mineralogical Association of America), PRESIDENT Michael J. Drake, University of Arizona and the journal Geochimica -
Download PDF About Minerals Sorted by Mineral Name
MINERALS SORTED BY NAME Here is an alphabetical list of minerals discussed on this site. More information on and photographs of these minerals in Kentucky is available in the book “Rocks and Minerals of Kentucky” (Anderson, 1994). APATITE Crystal system: hexagonal. Fracture: conchoidal. Color: red, brown, white. Hardness: 5.0. Luster: opaque or semitransparent. Specific gravity: 3.1. Apatite, also called cellophane, occurs in peridotites in eastern and western Kentucky. A microcrystalline variety of collophane found in northern Woodford County is dark reddish brown, porous, and occurs in phosphatic beds, lenses, and nodules in the Tanglewood Member of the Lexington Limestone. Some fossils in the Tanglewood Member are coated with phosphate. Beds are generally very thin, but occasionally several feet thick. The Woodford County phosphate beds were mined during the early 1900s near Wallace, Ky. BARITE Crystal system: orthorhombic. Cleavage: often in groups of platy or tabular crystals. Color: usually white, but may be light shades of blue, brown, yellow, or red. Hardness: 3.0 to 3.5. Streak: white. Luster: vitreous to pearly. Specific gravity: 4.5. Tenacity: brittle. Uses: in heavy muds in oil-well drilling, to increase brilliance in the glass-making industry, as filler for paper, cosmetics, textiles, linoleum, rubber goods, paints. Barite generally occurs in a white massive variety (often appearing earthy when weathered), although some clear to bluish, bladed barite crystals have been observed in several vein deposits in central Kentucky, and commonly occurs as a solid solution series with celestite where barium and strontium can substitute for each other. Various nodular zones have been observed in Silurian–Devonian rocks in east-central Kentucky. -
Washington State Minerals Checklist
Division of Geology and Earth Resources MS 47007; Olympia, WA 98504-7007 Washington State 360-902-1450; 360-902-1785 fax E-mail: [email protected] Website: http://www.dnr.wa.gov/geology Minerals Checklist Note: Mineral names in parentheses are the preferred species names. Compiled by Raymond Lasmanis o Acanthite o Arsenopalladinite o Bustamite o Clinohumite o Enstatite o Harmotome o Actinolite o Arsenopyrite o Bytownite o Clinoptilolite o Epidesmine (Stilbite) o Hastingsite o Adularia o Arsenosulvanite (Plagioclase) o Clinozoisite o Epidote o Hausmannite (Orthoclase) o Arsenpolybasite o Cairngorm (Quartz) o Cobaltite o Epistilbite o Hedenbergite o Aegirine o Astrophyllite o Calamine o Cochromite o Epsomite o Hedleyite o Aenigmatite o Atacamite (Hemimorphite) o Coffinite o Erionite o Hematite o Aeschynite o Atokite o Calaverite o Columbite o Erythrite o Hemimorphite o Agardite-Y o Augite o Calciohilairite (Ferrocolumbite) o Euchroite o Hercynite o Agate (Quartz) o Aurostibite o Calcite, see also o Conichalcite o Euxenite o Hessite o Aguilarite o Austinite Manganocalcite o Connellite o Euxenite-Y o Heulandite o Aktashite o Onyx o Copiapite o o Autunite o Fairchildite Hexahydrite o Alabandite o Caledonite o Copper o o Awaruite o Famatinite Hibschite o Albite o Cancrinite o Copper-zinc o o Axinite group o Fayalite Hillebrandite o Algodonite o Carnelian (Quartz) o Coquandite o o Azurite o Feldspar group Hisingerite o Allanite o Cassiterite o Cordierite o o Barite o Ferberite Hongshiite o Allanite-Ce o Catapleiite o Corrensite o o Bastnäsite -
Mineral Processing
Mineral Processing Foundations of theory and practice of minerallurgy 1st English edition JAN DRZYMALA, C. Eng., Ph.D., D.Sc. Member of the Polish Mineral Processing Society Wroclaw University of Technology 2007 Translation: J. Drzymala, A. Swatek Reviewer: A. Luszczkiewicz Published as supplied by the author ©Copyright by Jan Drzymala, Wroclaw 2007 Computer typesetting: Danuta Szyszka Cover design: Danuta Szyszka Cover photo: Sebastian Bożek Oficyna Wydawnicza Politechniki Wrocławskiej Wybrzeze Wyspianskiego 27 50-370 Wroclaw Any part of this publication can be used in any form by any means provided that the usage is acknowledged by the citation: Drzymala, J., Mineral Processing, Foundations of theory and practice of minerallurgy, Oficyna Wydawnicza PWr., 2007, www.ig.pwr.wroc.pl/minproc ISBN 978-83-7493-362-9 Contents Introduction ....................................................................................................................9 Part I Introduction to mineral processing .....................................................................13 1. From the Big Bang to mineral processing................................................................14 1.1. The formation of matter ...................................................................................14 1.2. Elementary particles.........................................................................................16 1.3. Molecules .........................................................................................................18 1.4. Solids................................................................................................................19 -
Role of Regional Ocean Dynamics in Dynamic Sea Level Projections by the End of the 21St Century Over Southeast Asia
EGU21-8618, updated on 25 Sep 2021 https://doi.org/10.5194/egusphere-egu21-8618 EGU General Assembly 2021 © Author(s) 2021. This work is distributed under the Creative Commons Attribution 4.0 License. Role of Regional Ocean Dynamics in Dynamic Sea Level Projections by the end of the 21st Century over Southeast Asia Dhrubajyoti Samanta1, Svetlana Jevrejeva2, Hindumathi K. Palanisamy2, Kristopher B. Karnauskas3, Nathalie F. Goodkin1,4, and Benjamin P. Horton1 1Nanyang Technological University, Singapore ([email protected]) 2Centre for Climate Research Singapore, Singapore 3University of Colorado Boulder, USA 4American Museum of Natural History, USA Southeast Asia is especially vulnerable to the impacts of sea-level rise due to the presence of many low-lying small islands and highly populated coastal cities. However, our current understanding of sea-level projections and changes in upper-ocean dynamics over this region currently rely on relatively coarse resolution (~100 km) global climate model (GCM) simulations and is therefore limited over the coastal regions. Here using GCM simulations from the High-Resolution Model Intercomparison Project (HighResMIP) of the Coupled Model Intercomparison Project Phase 6 (CMIP6) to (1) examine the improvement of mean-state biases in the tropical Pacific and dynamic sea-level (DSL) over Southeast Asia; (2) generate projection on DSL over Southeast Asia under shared socioeconomic pathways phase-5 (SSP5-585); and (3) diagnose the role of changes in regional ocean dynamics under SSP5-585. We select HighResMIP models that included a historical period and shared socioeconomic pathways (SSP) 5-8.5 future scenario for the same ensemble and estimate the projected changes relative to the 1993-2014 period. -
Depositional Setting of Algoma-Type Banded Iron Formation Blandine Gourcerol, P Thurston, D Kontak, O Côté-Mantha, J Biczok
Depositional Setting of Algoma-type Banded Iron Formation Blandine Gourcerol, P Thurston, D Kontak, O Côté-Mantha, J Biczok To cite this version: Blandine Gourcerol, P Thurston, D Kontak, O Côté-Mantha, J Biczok. Depositional Setting of Algoma-type Banded Iron Formation. Precambrian Research, Elsevier, 2016. hal-02283951 HAL Id: hal-02283951 https://hal-brgm.archives-ouvertes.fr/hal-02283951 Submitted on 11 Sep 2019 HAL is a multi-disciplinary open access L’archive ouverte pluridisciplinaire HAL, est archive for the deposit and dissemination of sci- destinée au dépôt et à la diffusion de documents entific research documents, whether they are pub- scientifiques de niveau recherche, publiés ou non, lished or not. The documents may come from émanant des établissements d’enseignement et de teaching and research institutions in France or recherche français ou étrangers, des laboratoires abroad, or from public or private research centers. publics ou privés. Accepted Manuscript Depositional Setting of Algoma-type Banded Iron Formation B. Gourcerol, P.C. Thurston, D.J. Kontak, O. Côté-Mantha, J. Biczok PII: S0301-9268(16)30108-5 DOI: http://dx.doi.org/10.1016/j.precamres.2016.04.019 Reference: PRECAM 4501 To appear in: Precambrian Research Received Date: 26 September 2015 Revised Date: 21 January 2016 Accepted Date: 30 April 2016 Please cite this article as: B. Gourcerol, P.C. Thurston, D.J. Kontak, O. Côté-Mantha, J. Biczok, Depositional Setting of Algoma-type Banded Iron Formation, Precambrian Research (2016), doi: http://dx.doi.org/10.1016/j.precamres. 2016.04.019 This is a PDF file of an unedited manuscript that has been accepted for publication. -
Download Service
Vol. 62 Bollettino Vol. 62 - SUPPLEMENT 1 pp. 327 di Geofisica An International teorica ed applicata Journal of Earth Sciences IMDIS 2021 International Conference on Marine Data and Information Systems 12-14 April, 2021 Online Book of Abstracts SUPPLEMENT 1 Guest Editors: Michèle Fichaut, Vanessa Tosello, Alessandra Giorgetti BOLLETTINO DI GEOFISICA teorica ed applicata 210109 - OGS.Supp.Vol62.cover_08dorso19.indd 3 03/05/21 10:54 EDITOR-IN-CHIEF D. Slejko; Trieste, Italy EDITORIAL COUNCIL SUBSCRIPTIONS 2021 A. Camerlenghi, N. Casagli, F. Coren, P. Del Negro, F. Ferraccioli, S. Parolai, G. Rossi, C. Solidoro; Trieste, Italy ASSOCIATE EDITORS A. SOLID EaRTH GeOPHYsICs N. Abu-Zeid; Ferrara, Italy J. Ba; Nanjing, China R. Barzaghi; Milano, Italy J. Boaga; Padova, Italy C. Braitenberg; Trieste, Italy A. Casas; Barcelona, Spain G. Cassiani; Padova, Italy F. Cavallini; Trieste, Italy A. Del Ben; Trieste, Italy P. dell’Aversana; San Donato Milanese, Italy C. Doglioni; Roma, Italy F. Ferrucci, Vibo Valentia, Italy E. Forte; Trieste, Italy M.-J. Jimenez; Madrid, Spain C. Layland-Bachmann, Berkeley, U.S.A. Bollettino di Geofisica Teorica ed Applicata G. Li; Zhoushan, China c/o Istituto Nazionale di Oceanografia P. Paganini; Trieste, Italy e di Geofisica Sperimentale V. Paoletti, Naples, Italy Borgo Grotta Gigante, 42/c E. Papadimitriou; Thessaloniki, Greece 34010 Sgonico, Trieste, Italy R. Petrini; Pisa, Italy e-mail: [email protected] M. Pipan; Trieste, Italy G. Seriani; Trieste, Italy http-server: bgta.eu A. Shogenova; Tallin, Estonia E. Stucchi; Milano, Italy S. Trevisani; Venezia, Italy M. Vellico; Trieste, Italy A. Vesnaver; Trieste, Italy V. Volpi; Trieste, Italy A. -
Arsenian Sphalerite from Mina Ai,Caran, Pampa Larga
MINERALOGICAL NOTES AMERICAN MINERALOGIST, \IOL. 55, SEPTEMBER.OCTOBER, 1970 ARSENIANSPHALERITE FROM MINA AI,CARAN, PAMPALARGA, COPIAPO, CHILE Arew H. Cr-anr, Department oJ GeologicalSciences, Queen's Uniaersity, Kingston, Ontario, Canado. ABSTRACT Bright pink sphalerite from the arsenic-rich Alacr6n deposit, with a:5.4110 +0.0003 A, is shown by electron-probe microanalysis to contain only traces of iron but 17 +0.3 weight percent As INrnooucrroN The literature containsnumerous reports of appreciablesolid solution of arsenicin sphalerite(e.g. Schroll, 1953; Fleischer,1955), but the an- alytical evidenceremains largeiy unconvincing.Moss (1955;and in Hey, 1955,Frondel, 1967)proposed that the mineral voltzite has the general composition (Zn,As)S or Zn(As,S), but Frondel (1967) subsequently found no evidenceto support this suggestion.Most recent electron- probe microanalysesof sphaleritedo not record even traces of arsentc. Ilowever, Herzenberg(1932,1933) found 0.64 weight percentarsenic by chemical analysisof a raspberry-redsphalerite-like mineral from Llall- agua, Bolivia, which he named gumuc'ionite.Later workers (e.g.Hey, 1955)have assumedthat this material representsa mixture of sphalerite and realgarbut no further work appearsto have been carried out on the original or similar specimens.The presentnote describesthe occurrence of an apparently similar, and demonstrably arsenic-bearingsphalerite. Spner-Bnrrr rN rHE Ar,acnAN DBposrr Sphalerite is a minor constituent of the mineralogically complex, polymetallic Alacr6n vein deposit (Parker, Salas and P6rez, 1963),in the Pampa Larga mining district of northern Chile (Lat. 27"36'5.;Long. 70'11'W.). It occurs, however, in at least three parageneticcontexts: (1) in associationwith early arsenopyrite, pyrite, stibnite, smithite, aAsS (Clark, 1970a)and arsenolamprite(Clark, 1970b), among other minerals; (2) with late-stagegreigite, pyrite, native arsenic,realgar, and orpiment;and (3) rarely, as free-standingcrystals in vugs, in association with realgar and orpiment. -
Shallow Water Waves and Solitary Waves Article Outline Glossary
Shallow Water Waves and Solitary Waves Willy Hereman Department of Mathematical and Computer Sciences, Colorado School of Mines, Golden, Colorado, USA Article Outline Glossary I. Definition of the Subject II. Introduction{Historical Perspective III. Completely Integrable Shallow Water Wave Equations IV. Shallow Water Wave Equations of Geophysical Fluid Dynamics V. Computation of Solitary Wave Solutions VI. Water Wave Experiments and Observations VII. Future Directions VIII. Bibliography Glossary Deep water A surface wave is said to be in deep water if its wavelength is much shorter than the local water depth. Internal wave A internal wave travels within the interior of a fluid. The maximum velocity and maximum amplitude occur within the fluid or at an internal boundary (interface). Internal waves depend on the density-stratification of the fluid. Shallow water A surface wave is said to be in shallow water if its wavelength is much larger than the local water depth. Shallow water waves Shallow water waves correspond to the flow at the free surface of a body of shallow water under the force of gravity, or to the flow below a horizontal pressure surface in a fluid. Shallow water wave equations Shallow water wave equations are a set of partial differential equations that describe shallow water waves. 1 Solitary wave A solitary wave is a localized gravity wave that maintains its coherence and, hence, its visi- bility through properties of nonlinear hydrodynamics. Solitary waves have finite amplitude and propagate with constant speed and constant shape. Soliton Solitons are solitary waves that have an elastic scattering property: they retain their shape and speed after colliding with each other. -
Using the High-Temperature Phase Transition of Iron Sulfide Minerals As
www.nature.com/scientificreports OPEN Using the high-temperature phase transition of iron sulfde minerals as an indicator of fault Received: 9 November 2018 Accepted: 15 May 2019 slip temperature Published: xx xx xxxx Yan-Hong Chen1, Yen-Hua Chen1, Wen-Dung Hsu2, Yin-Chia Chang2, Hwo-Shuenn Sheu3, Jey-Jau Lee3 & Shih-Kang Lin2 The transformation of pyrite into pyrrhotite above 500 °C was observed in the Chelungpu fault zone, which formed as a result of the 1999 Chi-Chi earthquake in Taiwan. Similarly, pyrite transformation to pyrrhotite at approximately 640 °C was observed during the Tohoku earthquake in Japan. In this study, we investigated the high-temperature phase-transition of iron sulfde minerals (greigite) under anaerobic conditions. We simulated mineral phase transformations during fault movement with the aim of determining the temperature of fault slip. The techniques used in this study included thermogravimetry and diferential thermal analysis (TG/DTA) and in situ X-ray difraction (XRD). We found diversifcation between 520 °C and 630 °C in the TG/DTA curves that signifes the transformation of pyrite into pyrrhotite. Furthermore, the in situ XRD results confrmed the sequence in which greigite underwent phase transitions to gradually transform into pyrite and pyrrhotite at approximately 320 °C. Greigite completely changed into pyrite and pyrrhotite at 450 °C. Finally, pyrite was completely transformed into pyrrhotite at 580 °C. Our results reveal the temperature and sequence in which the phase transitions of greigite occur, and indicate that this may be used to constrain the temperature of fault-slip. This conclusion is supported by feld observations made following the Tohoku and Chi-Chi earthquakes. -
FREE MACKINAWITE FREE SULFIDATED IRON When and Where You Want It
FREE MACKINAWITE FREE SULFIDATED IRON when and where you want it REACTIVE IRON SULFIDES As reviewed by Fan et al., (2017), multiple studies have shown that various reactive iron sulfide species can aid in the biogeochemical transformation of organic constituents of interest (COIs) such as halogenated organic solvents, and that they can be useful in precipitating inorganic COIs such as arsenic, chromium and mercury. This is most apparent with nanoscale or fine (e.g., < 10 micron) zero valent iron (ZVI) particles because they have more surface area which can be quickly passivated, hence within a short period of time, they typically exhibit lower efficiency for dechlorination. In an effort to mitigate this phenomenon various formulations of sulfidated iron (S-ZVI) and other reactive iron sulfide species such as mackinawite per se have become available commercially as remedial amendments designed to be injected or otherwise applied directly to an impacted environment. The reactive properties of S-ZVI adhere to classic corrosion chemistry principles governing the conditions under which sulfur attacks iron. Recognizing the potential distinctions between chemical sulfidation and natural sulfidation, an alternative means of harnessing the activity of reactive iron sulfides - instead of buying mackinawite alone (for example) - is to generate multiple iron sulfide species, in place, and for free as part of an engineered remedial amendment that integrates multiple synergistic biogeochemical reactions (see Mangayayam et al, 2019 for emerging insights into the actual value of buying and applying sulfidated iron products directly). In so doing the remedial actions occur where they are needed and not simply where the insoluble precipitates are directly emplaced. -
Infrare D Transmission Spectra of Carbonate Minerals
Infrare d Transmission Spectra of Carbonate Mineral s THE NATURAL HISTORY MUSEUM Infrare d Transmission Spectra of Carbonate Mineral s G. C. Jones Department of Mineralogy The Natural History Museum London, UK and B. Jackson Department of Geology Royal Museum of Scotland Edinburgh, UK A collaborative project of The Natural History Museum and National Museums of Scotland E3 SPRINGER-SCIENCE+BUSINESS MEDIA, B.V. Firs t editio n 1 993 © 1993 Springer Science+Business Media Dordrecht Originally published by Chapman & Hall in 1993 Softcover reprint of the hardcover 1st edition 1993 Typese t at the Natura l Histor y Museu m ISBN 978-94-010-4940-5 ISBN 978-94-011-2120-0 (eBook) DOI 10.1007/978-94-011-2120-0 Apar t fro m any fair dealin g for the purpose s of researc h or privat e study , or criticis m or review , as permitte d unde r the UK Copyrigh t Design s and Patent s Act , 1988, thi s publicatio n may not be reproduced , stored , or transmitted , in any for m or by any means , withou t the prio r permissio n in writin g of the publishers , or in the case of reprographi c reproductio n onl y in accordanc e wit h the term s of the licence s issue d by the Copyrigh t Licensin g Agenc y in the UK, or in accordanc e wit h the term s of licence s issue d by the appropriat e Reproductio n Right s Organizatio n outsid e the UK. Enquirie s concernin g reproductio n outsid e the term s state d here shoul d be sent to the publisher s at the Londo n addres s printe d on thi s page.