Petrography and Engineering Properties of Igneous Rocks
Total Page:16
File Type:pdf, Size:1020Kb
Load more
Recommended publications
-
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. -
Geologic Storage Formation Classification: Understanding Its Importance and Impacts on CCS Opportunities in the United States
BEST PRACTICES for: Geologic Storage Formation Classification: Understanding Its Importance and Impacts on CCS Opportunities in the United States First Edition Disclaimer This report was prepared as an account of work sponsored by an agency of the United States Government. Neither the United States Government nor any agency thereof, nor any of their employees, makes any warranty, express or implied, or assumes any legal liability or responsibility for the accuracy, completeness, or usefulness of any information, apparatus, product, or process disclosed, or represents that its use would not infringe privately owned rights. Reference therein to any specific commercial product, process, or service by trade name, trademark, manufacturer, or otherwise does not necessarily constitute or imply its endorsement, recommendation, or favoring by the United States Government or any agency thereof. The views and opinions of authors expressed therein do not necessarily state or reflect those of the United States Government or any agency thereof. Cover Photos—Credits for images shown on the cover are noted with the corresponding figures within this document. Geologic Storage Formation Classification: Understanding Its Importance and Impacts on CCS Opportunities in the United States September 2010 National Energy Technology Laboratory www.netl.doe.gov DOE/NETL-2010/1420 Table of Contents Table of Contents 5 Table of Contents Executive Summary ____________________________________________________________________________ 10 1.0 Introduction and Background -
Geochemistry of Granitic Aplite-Pegmatite Veins and Sills and Their Minerals from the Sabugal Area, Central Portugal
N. Jb. Miner. Abh. 188/3, 297 – 316 Fast Track Article PublishedStuttgart, Augustonline November2011 2011 Geochemistry of granitic aplite-pegmatite veins and sills and their minerals from the Sabugal area, central Portugal Ana M. R. Neiva, Paulo B. Silva and João M. F. Ramos With 19 fi gures and 12 tables Abstract: Granitic beryl-columbite-phosphate subtype aplite-pegmatite veins and sills from the Sabugal area intruded a biotite > muscovite granite which is related to another two-mica granite. Variation diagrams of major and trace elements of whole rocks δ18 show fractionation trends. REE patterns and O of whole rocks, BaO and P2O5 contents of K-feldspar, anorthite and P2O5 contents of plagioclase, major element and Li contents of muscovite and lithian muscovite support this series. Least squares analysis of ma- jor elements indicate that the biotite > muscovite granite and aplite-pegmatite veins and sills are derived from the earlier two-mica granite magma by fractional crystallization of quartz, plagioclase, K-feldspar, biotite and ilmenite. Modelling of trace elements shows that magmatic fl uxes and fl uids controlled the Rb, Sr and Ba contents of aplite-pegmatites,Paper probably also lithium micas (zin- nwaldite, polylithionite and rare lepidolite), cassiterite, columbite-tantalite, fl uorapatite and triplite. In aplite-pegmatites, lithian muscovite replaces primary muscovite and late lithium micas replace lithian muscovite. Complexely zoned columbite crystals are chemically characterized and attributed to disequilibrium conditions. Relations of granites and aplite-pegmatites and pegmatites from other Portuguese and Spanish areas are compared. The granitic aplite-pegmatites from Sabugal are moderately fractionated and the granitic complex type aplite-pegmatites from Gonçalo are the richest in Li and Sn, derived from a higher degree of frac- tional crystallization and fl uxes and fl uids control the Ba and Rb behaviours and Li, Sn, F and Ta concentrations. -
The Forsterite-Anorthite-Albite System at 5 Kb Pressure Kristen Rahilly
The Forsterite-Anorthite-Albite System at 5 kb Pressure Kristen Rahilly Submitted to the Department of Geosciences of Smith College in partial fulfillment of the requirements for the degree of Bachelor of Arts John B. Brady, Honors Project Advisor Acknowledgements First I would like to thank my advisor John Brady, who patiently taught me all of the experimental techniques for this project. His dedication to advising me through this thesis and throughout my years at Smith has made me strive to be a better geologist. I would like to thank Tony Morse at the University of Massachusetts at Amherst for providing all of the feldspar samples and for his advice on this project. Thank you also to Michael Jercinovic over at UMass for his help with last-minute carbon coating. This project had a number of facets and I got assistance from many different departments at Smith. A big thank you to Greg Young and Dale Renfrow in the Center for Design and Fabrication for patiently helping me prepare and repair the materials needed for experiments. I’m also grateful to Dick Briggs and Judith Wopereis in the Biology Department for all of their help with the SEM and carbon coater. Also, the Engineering Department kindly lent their copy of LabView software for this project. I appreciated the advice from Mike Vollinger within the Geosciences Department as well as his dedication to driving my last three samples over to UMass to be carbon coated. The Smith Tomlinson Fund provided financial support. Finally, I need to thank my family for their support and encouragement as well as my friends here at Smith for keeping this year fun and for keeping me balanced. -
Decrepitation Characteristics of Igneous
DECREPITATIONCHARACTERISTICS OF IGNEOUSROCKS F. G. SMITH Unfuersi,tyof Toronto, Toronto, Canada Ansrnect ._lecrepitation during heating of igneous intrusive rocks is complex, but one stage (D2) appears to be due to misfit of solid inclusions. This stage begins at 6rb + g0'-b in simple granite pegmatite and aplite, Z0S * 80" C in ganiie, Z6E + 50" C in granodiorite and quartz norite, and 1010 + 60o C in gabbro and related rocks. The p2-sQS! of pegmatite and aplite in an area of migmatitic gneiss, with no exposed batholiths, starts at a lower temperature than the corresponding stage of decrepitation of the country gneiss. Introd,wction The rationale of decrepitation due to misfit of solid inclusions in minerals, when heated above the temperature of crystallization, was outlined previously (smith, L952a).A stage of decrepitation of several types of garnet was interpreted to be due to solid inclusions, becausethe frequency of decrepitation was found to be directly related to the abundanceof solid inclusions (smith, lg52b). A similar stage of decrepi- tation of high grade metamorphic rocks was found (Smith, lgb8). The measuredtemperatures of the beginning of this stage of decrepitation of metamorphic minerals are internally consistent, and are not at variance with the small amount of synthetic data. As a further test of the rationale. a few rocks representing several igneous rock clans were heated in the decrepitation apparatus. The results can be interpreted in an analogous manner to give the temperature of crystallization of the constituent minerals. These data, which should be considered as only tentative becauseof the small number in each clan tested, are given below, uncor- rected for the effect of pressiure. -
Summary of the Mineral Information Package for the Khanneshin Carbonatite Area of Interest
Chapter 21A. Summary of the Mineral Information Package for the Khanneshin Carbonatite Area of Interest Contribution by Robert D. Tucker, Harvey E. Belkin, Klaus J. Schulz, Stephen G. Peters, and Kim P. Buttleman Abstract The Khanneshin carbonatite is a deeply dissected igneous complex of Quaternary age that rises approximately 700 meters above the flat-lying Neogene sediments of the Registan Desert, Helmand Province, Afghanistan. The complex consists almost exclusively of carbonate-rich intrusive and extrusive igneous rocks, crudely circular in outline, with only three small hypabyssal plugs of leucite phonolite and leucitite outcropping in the southeastern part of the complex. The complex is broadly divisible into a central intrusive vent (or massif), approximately 4 kilometers in diameter, consisting of coarse-grained sövite and brecciated and agglomeratic barite-ankerite alvikite; a thin marginal zone (less than 1 kilometer wide) of outwardly dipping (5°–45°). Neogene sedimentary strata; and a peripheral apron of volcanic and volcaniclastic strata extending another 3–5 kilometers away from the central intrusive massif. Small satellitic intrusions of biotite-calcite carbonatite, no larger than 400 meters in diameter, crop out on the southern and southeastern margin of the central intrusive massif. In the 1970s several teams of Soviet geologists identified prospective areas of interest for uranium, phosphorus, and light rare earth element (LREE) mineralization in four regions of the carbonatite complex. High uranium concentrations are reported in two regions; the greatest concentrations are confined to silicified shear zones in sandy clay approximately 1.1 kilometers southwest of the peripheral part of the central vent. An area of phosphorus enrichment, primarily occurring in apatite, is present in coarse-grained agglomeratic alvikite, with abundant fenite xenoliths, approximately 750 meters south of the periphery of the central vent. -
Geology of the Nairobi Region, Kenya
% % % % % % % % %% %% %% %% %% %% %% % GEOLOGIC HISTORY % %% %% % % Legend %% %% %% %% %% %% %% % % % % % % HOLOCENE: %% % Pl-mv Pka %%% Sediments Mt Margaret U. Kerichwa Tuffs % % % % %% %% % Longonot (0.2 - 400 ka): trachyte stratovolcano and associated deposits. Materials exposed in this map % %% %% %% %% %% %% % section are comprised of the Longonot Ash Member (3.3 ka) and Lower Trachyte (5.6-3.3 ka). The % Pka' % % % % % % L. Kerichwa Tuff % % % % % % Alluvial fan Pleistocene: Calabrian % % % % % % % Geo% lo% gy of the Nairobi Region, Kenya % trachyte lavas were related to cone building, and the airfall tuffs were produced by summit crater formation % % % % % % % % % % % % % % % % % Pna % % % % %% % (Clarke et al. 1990). % % % % % % Pl-tb % % Narok Agglomerate % % % % % Kedong Lake Sediments Tepesi Basalt % % % % % % % % % % % % % % % % %% % % % 37.0 °E % % % % 36.5 °E % % % % For area to North see: Geology of the Kijabe Area, KGS Report 67 %% % % % Pnt %% % PLEISTOCENE: % % %% % % % Pl-kl %% % % Nairobi Trachyte % %% % -1.0 ° % % % % -1.0 ° Lacustrine Sediments % % % % % % % % Pleistocene: Gelasian % % % % % Kedong Valley Tuff (20-40 ka): trachytic ignimbrites and associated fall deposits created by caldera % 0 % 1800 % % ? % % % 0 0 % % % 0 % % % % % 0 % 0 8 % % % % % 4 % 4 Pkt % formation at Longonot. There are at least 5 ignimbrite units, each with a red-brown weathered top. In 1 % % % % 2 % 2 % % Kiambu Trachyte % Pl-lv % % % % % % % % % % %% % % Limuru Pantellerite % % % % some regions the pyroclastic glass and pumice has been -
The Surface Reactions of Silicate Minerals
RESEARCH BULLETIN 614 SEPTEMBER, 1956 UNIVERSITY OF MISSOURI COLLEGE OF AGRICULTURE AGRICULTURAL EXPERIMENT STATION J. H. Longwell, Director The Surface Reactions Of Silicate Minerals PART II. REACTIONS OF FELDSPAR SURFACES WITH SALT SOLUTIONS. V. E. NASH AND C. E. MARSHALL (Publication authorized September 5, 1956) COLUMBIA, MISSOURI TABLE OF CONTENTS Introduction .......... .. 3 The Interaction of Albite with Salt Solutions . .. 4 The Interaction of Anorthite with Salt Solutions ........ .. 7 Relative Effectiveness of Ammonium Chloride and Magnesium Chloride on the Release of Sodium from Albite . .. 9 Surface Interaction of Albite with Salt Solutions in Methanol . .. 13 Experiments on Cationic Fixation ............................... 16 Detailed Exchange and Activity Studies with Individual Feldspars .......... .. 19 Procedure .. .. 20 Microcline . .. 21 Albite .................................................... 22 Oligoclase . .. 23 Andesine . .. 24 Labradori te . .. 25 Bytownite ................................................. 25 Anorthite . .. 27 Discussion ........ .. 28 Summary ..................................................... 35 References .. .. 36 Most of the experimental material of this and the preceding Research Bulletin is taken from the Ph.D. Thesis of Victor Nash, University of Missouri, June 1955. The experiments on cation fixation were carried our with the aid of a research grant from the Potash Rock Company of America, Lithonia, Georgia, for which the authors wish to record their appreciation. The work was part of Department of Soils Research Project No.6, entitled, "Heavy Clays." The Surface Reactions of Silicate Minerals PART II. REACTIONS OF FELDSPAR SURFACES WITH SALT SOLUTIONS. v. E. NASH AND C. E. MARSHALL INTRODUCTION The review of literature cited in Part I of this series indicates that little is known of the interaction of feldspar surfaces with salt solutions. The work of Breazeale and Magistad (1) clearly demonstrated that ex change reactions between potassium and calcium occur in the case of or thoclase surfaces. -
Noritic Anorthosite Bodies in the Sierra Nevada Batholith
MINERALOGICAL SOCIETY OF AMERICA, SPECIAL PAPER 1, 1963 INTERNATIONALMINERALOGICAL ASSOCIATION,PAPERS, THIRD GENERAL MEETING NORITIC ANORTHOSITE BODIES IN THE SIERRA NEVADA BATHOLITH ALDEN A. LOOMISl Department of Geology, Stanford University, Stanford, California ABSTRACT A group of small noritic plutons were intruded prior to the immediately surrounding granitic rocks in a part of the composite Sierra Nevada batholith near Lake Tahoe. Iron was more strongly concentrated in the late fluids of individual bodies than during the intrusive sequence as a whole. Pyroxenes are more ferrous in rocks late in the sequence, although most of the iron is in late magnetite which replaces pyroxenes. Both Willow Lake type and normal cumulative layering are present. Cumulative layering is rare; Willi ow Lake layering is common and was formed early in individual bodies. Willow Lake layers require a compositional uniqueness providing high ionic mobility to explain observed relations. The Sierran norites differ from those in large stratiform plutons in that (1) the average bulk composition is neritic anorthosite in which typical rocks contain over 20% AbO" and (2) differentiation of both orthopyroxene and plagioclase produced a smooth progressive sequence of mineral compositions. A plot of modal An vs. En for all the rocks in the sequence from early Willow Lake-type layers to late no rite dikes defines a smooth non-linear trend from Anss-En76 to An,,-En54. TLe ratio An/ Ab decreased faster than En/Of until the assemblage Anso-En65 was reached and En/Of began to decrease more rapidly. Similar plots for large stratiform bodies show too much scatter to define single curves. -
Module 7 Igneous Rocks IGNEOUS ROCKS
Module 7 Igneous Rocks IGNEOUS ROCKS ▪ Igneous Rocks form by crystallization of molten rock material IGNEOUS ROCKS ▪ Igneous Rocks form by crystallization of molten rock material ▪ Molten rock material below Earth’s surface is called magma ▪ Molten rock material erupted above Earth’s surface is called lava ▪ The name changes because the composition of the molten material changes as it is erupted due to escape of volatile gases Rocks Cycle Consolidation Crystallization Rock Forming Minerals 1200ºC Olivine High Ca-rich Pyroxene Ca-Na-rich Amphibole Intermediate Na-Ca-rich Continuous branch Continuous Discontinuous branch Discontinuous Biotite Na-rich Plagioclase feldspar of liquid increases liquid of 2 Temperature decreases Temperature SiO Low K-feldspar Muscovite Quartz 700ºC BOWEN’S REACTION SERIES Rock Forming Minerals Olivine Ca-rich Pyroxene Ca-Na-rich Amphibole Na-Ca-rich Continuous branch Continuous Discontinuous branch Discontinuous Biotite Na-rich Plagioclase feldspar K-feldspar Muscovite Quartz BOWEN’S REACTION SERIES Rock Forming Minerals High Temperature Mineral Suite Olivine • Isolated Tetrahedra Structure • Iron, magnesium, silicon, oxygen • Bowen’s Discontinuous Series Augite • Single Chain Structure (Pyroxene) • Iron, magnesium, calcium, silicon, aluminium, oxygen • Bowen’s Discontinuos Series Calcium Feldspar • Framework Silicate Structure (Plagioclase) • Calcium, silicon, aluminium, oxygen • Bowen’s Continuous Series Rock Forming Minerals Intermediate Temperature Mineral Suite Hornblende • Double Chain Structure (Amphibole) -
Siluro-Devonian Igneous Rocks of the Easternmost Three Terranes in Southeastern New England: Examples from Ne Massachusetts and Se New Hampshire
SILURO-DEVONIAN IGNEOUS ROCKS OF THE EASTERNMOST THREE TERRANES IN SOUTHEASTERN NEW ENGLAND: EXAMPLES FROM NE MASSACHUSETTS AND SE NEW HAMPSHIRE by Rudolph Hon, Department of Geology and Geophysics, Boston College, Chestnut Hill, MA 02467 J. Christopher Hepburn, Dept. of Geology and Geophysics, Boston College, Chestnut Hill, MA 02467 Jo Laird, Dept. of Earth Sciences, University of New Hampshire, Durham, NH 03824 INTRODUCTION Siluro-Devonian igneous rocks in northeastern Massachusetts and adjacent southern New Hampshire have been the subject of mineralogical, petrological and geological studies for over 150 years (Rodgers et al., 1989; Brady and Cheney, 2004), but only in recent times has it been recognized that these rocks lie in three distinct geological terranes. These rocks include a diverse variety of plutonic and volcanic rocks ranging in chemistry from peralkaline to calc-alkaline. Of particular note are the widely known mid-Paleozoic alkaline plutons that include the type localities of both the rock “essexite,” nepheline monzogabbro to nepheline monzodiorite (Sears, 1891), and the mineral “annite,” iron biotite (Dana, 1868). This field excursion is designed to demonstrate the diversity of the igneous rocks in the area and to visit (weather permitting) some of the classic localities. Throughout the excursion, the relationship of the timing and petrogenesis of the magmatism to the tectonics will be considered. It is impossible to exhaustibly discuss or credit all the work that has led to our current understanding of the igneous rocks in this region. The list includes many petrologists such as H.S. Washington, N. S. Shaler, C. H. Clapp, N. L. Bowen, J. -
Mid-Infrared Optical Constants of Clinopyroxene and Orthoclase Derived from Oriented Single-Crystal Reflectance Spectra
American Mineralogist, Volume 99, pages 1942–1955, 2014 Mid-infrared optical constants of clinopyroxene and orthoclase derived from oriented single-crystal reflectance spectra JESSICA A. ARNOLD1,*, TIMOTHY D. GLOTCH1 AND ANNA M. PLONKA1 1Department of Geosciences, Stony Brook University, Stony Brook, New York 11794, U.S.A. ABSTRACT We have determined the mid-IR optical constants of one alkali feldspar and four pyroxene compo- sitions in the range of 250–4000 cm–1. Measured reflectance spectra of oriented single crystals were iteratively fit to modeled spectra derived from classical dispersion analysis. We present the real and imaginary indices of refraction (n and k) along with the oscillator parameters with which they were modeled. While materials of orthorhombic symmetry and higher are well covered by the current literature, optical constants have been derived for only a handful of geologically relevant monoclinic materials, including gypsum and orthoclase. Two input parameters that go into radiative transfer models, the scattering phase function and the single scattering albedo, are functions of a material’s optical constants. Pyroxene is a common rock-forming mineral group in terrestrial bodies as well as meteorites and is also detected in cosmic dust. Hence, having a set of pyroxene optical constants will provide additional details about the composition of Solar System bodies and circumstellar materials. We follow the method of Mayerhöfer et al. (2010), which is based on the Berreman 4 × 4 matrix formulation. This approach provides a consistent way to calculate the reflectance coefficients in low- symmetry cases. Additionally, while many models assume normal incidence to simplify the dispersion relations, this more general model applies to reflectance spectra collected at non-normal incidence.