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How to Identify Rocks and Minerals
How to Identify Rocks and Minerals fluorite calcite epidote quartz gypsum pyrite copper fluorite galena By Jan C. Rasmussen (Revised from a booklet by Susan Celestian) 2012 Donations for reproduction from: Freeport McMoRan Copper & Gold Foundation Friends of the Arizona Mining & Mineral Museum Wickenburg Gem & Mineral Society www.janrasmussen.com ii NUMERICAL LIST OF ROCKS & MINERALS IN KIT See final pages of book for color photographs of rocks and minerals. MINERALS: IGNEOUS ROCKS: 1 Talc 2 Gypsum 50 Apache Tear 3 Calcite 51 Basalt 4 Fluorite 52 Pumice 5 Apatite* 53 Perlite 6 Orthoclase (feldspar group) 54 Obsidian 7 Quartz 55 Tuff 8 Topaz* 56 Rhyolite 9 Corundum* 57 Granite 10 Diamond* 11 Chrysocolla (blue) 12 Azurite (dark blue) METAMORPHIC ROCKS: 13 Quartz, var. chalcedony 14 Chalcopyrite (brassy) 60 Quartzite* 15 Barite 61 Schist 16 Galena (metallic) 62 Marble 17 Hematite 63 Slate* 18 Garnet 64 Gneiss 19 Magnetite 65 Metaconglomerate* 20 Serpentine 66 Phyllite 21 Malachite (green) (20) (Serpentinite)* 22 Muscovite (mica group) 23 Bornite (peacock tarnish) 24 Halite (table salt) SEDIMENTARY ROCKS: 25 Cuprite 26 Limonite (Goethite) 70 Sandstone 27 Pyrite (brassy) 71 Limestone 28 Peridot 72 Travertine (onyx) 29 Gold* 73 Conglomerate 30 Copper (refined) 74 Breccia 31 Glauberite pseudomorph 75 Shale 32 Sulfur 76 Silicified Wood 33 Quartz, var. rose (Quartz, var. chert) 34 Quartz, var. amethyst 77 Coal 35 Hornblende* 78 Diatomite 36 Tourmaline* 37 Graphite* 38 Sphalerite* *= not generally in kits. Minerals numbered 39 Biotite* 8-10, 25, 29, 35-40 are listed for information 40 Dolomite* only. www.janrasmussen.com iii ALPHABETICAL LIST OF ROCKS & MINERALS IN KIT See final pages of book for color photographs of rocks and minerals. -
Impacts of Sedimentation and Drivers of Variability in the Boulder Patch
Environmental Studies Program: Ongoing Study Title Impacts of Sedimentation and Drivers of Variability in the Boulder Patch Community, Beaufort Sea (AK-19-01) Administered by Anchorage, Alaska Office BOEM Contact(s) Rick Raymond [email protected] Conducting Organizations(s) University of Texas at Austin and UAF Total BOEM Cost $750,000 Performance Period FY 2019–2024 Final Report Due June 2024 Date Revised October 4, 2019 PICOC Summary Problem The Boulder Patch provides complex and unique habitat and supports high biodiversity in an area of considerable oil and gas interest, which includes the proposed construction of Liberty Island (less than half a mile away). Impacts of industry activity may smother/bury/kill productive biological area, but mitigation measures may be possible. Intervention This study will conduct a monitoring program to examine long-term drivers of community variability during Liberty development activities. In addition, it will test possible mitigation measures using common industry materials to “reseed” or replace habitat lost due to Liberty Island development activities. Comparison The post-development community structure will be compared against historic data to assess impacts of O&G activity. Further, artificial substrate will be compared to buried boulders to test efficacy of using industry materials to mitigate development impacts. Outcome Results will include defined spatial gradients and temporal trends in environmental conditions, benthic community structure, and kelp production in the Boulder Patch community; evaluation of the effect of sediments on Boulder Patch community; and assessment of test artificial substrates as possible habitat mitigation. Context Impacts of Sedimentation and Drivers of Variability in the Boulder Patch Community, Beaufort Sea (AK-19-01) BOEM Information Need(s): Impacts to the Boulder Patch from proposed gravel island construction were identified by local communities as a concern during scoping for Liberty Island. -
17. Clay Mineralogy of Deep-Sea Sediments in the Northwestern Pacific, Dsdp, Leg 20
17. CLAY MINERALOGY OF DEEP-SEA SEDIMENTS IN THE NORTHWESTERN PACIFIC, DSDP, LEG 20 Hakuyu Okada and Katsutoshi Tomita, Department of Geology, Kagoshima University, Kagoshima 890, Japan INTRODUCTION intensity of montmorillonite can be obtained by sub- tracting the (001) reflection intensity of chlorite from the Clay mineral study of samples collected during Leg 20 of preheating or pretreating reflection intensity at 15 Å. the Deep Sea Drilling Project in the western north Pacific In a specimen with coexisting kaolinite and chlorite, was carried out mainly by means of X-ray diffraction their overlapping reflections make it difficult to determine analyses. Emphasis was placed on determining vertical quantitatively these mineral compositions. For such speci- changes in mineral composition of sediments at each site. mens Wada's method (Wada, 1961) and heat treatment Results of the semiquantitative and quantitative deter- were adopted. minations of mineral compositions of analyzed samples are The following shows examples of the determination of shown in Tables 1, 2, 3, 5, and 7. The mineral suites some intensity ratios of reflections of clay minerals. presented here show some unusual characters as discussed below. The influence of burial diagenesis is also evidenced Case 1 in the vertical distribution of some authigenic minerals. Montmorillonite (two layers of water molecules between These results may contribute to a better understanding silicate layers)—kaolinite mixture. of deep-sea sedimentation on the northwestern Pacific This is the situation in which samples contain both plate. montmorillonite and kaolinite. The first-order basal reflec- tions of these minerals do not overlap. When the (002) ANALYTICAL PROCEDURES reflection of montmorillonite, which appears at about 7 Å, Each sample was dried in air, and X-ray diffraction is absent or negligible, the intensity ratio is easily obtained. -
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. -
The Lithostratigraphy and Biostratigraphy of the Chalk Group (Upper Coniacian 1 to Upper Campanian) at Scratchell’S Bay and Alum Bay, Isle of Wight, UK
Manuscript Click here to view linked References The lithostratigraphy and biostratigraphy of the Chalk Group (Upper Coniacian 1 to Upper Campanian) at Scratchell’s Bay and Alum Bay, Isle of Wight, UK. 2 3 Peter Hopson1*, Andrew Farrant1, Ian Wilkinson1, Mark Woods1 , Sev Kender1 4 2 5 and Sofie Jehle , 6 7 1 British Geological Survey, Sir Kingsley Dunham Centre, Nottingham, NG12 8 5GG. 9 2 10 University of Tübingen, Sigwartstraße 10, 72074 Tübingen, Germany 11 12 * corresponding author [email protected] 13 14 Keywords: Cretaceous, Isle of Wight, Chalk, lithostratigraphy, biostratigraphy, 15 16 17 Abstract 18 19 The Scratchell‟s Bay and southern Alum Bay sections, in the extreme west of the Isle 20 21 of Wight on the Needles promontory, cover the stratigraphically highest Chalk Group 22 formations available in southern England. They are relatively inaccessible, other than 23 by boat, and despite being a virtually unbroken succession they have not received the 24 attention afforded to the Whitecliff GCR (Geological Conservation Review series) 25 site at the eastern extremity of the island. A detailed account of the lithostratigraphy 26 27 of the strata in Scratchell‟s Bay is presented and integrated with macro and micro 28 biostratigraphical results for each formation present. Comparisons are made with 29 earlier work to provide a comprehensive description of the Seaford Chalk, Newhaven 30 Chalk, Culver Chalk and Portsdown Chalk formations for the Needles promontory. 31 32 33 The strata described are correlated with those seen in the Culver Down Cliffs – 34 Whitecliff Bay at the eastern end of the island that form the Whitecliff GCR site. -
Mineral Quantification with Simultaneous Refinement of Ca-Mg Carbonates Non-Stoichiometry by X-Ray Diffraction, Rietveld Method
Article Mineral Quantification with Simultaneous Refinement of Ca-Mg Carbonates Non-Stoichiometry by X-ray Diffraction, Rietveld Method Hélisson Nascimento dos Santos 1,*, Reiner Neumann 1,2 and Ciro Alexandre Ávila 2 1 CETEM—Centre for Mineral Technology, Division for Technological Characterisation, 22461-908 Rio de Janeiro, Brazil; [email protected] 2 Museu Nacional, Universidade Federal do Rio de Janeiro, 20940-040 Rio de Janeiro, Brazil; [email protected] * Correspondence: [email protected]; Tel.: +51-21-3865-7263 Received: 3. July 2017; Accepted: 4 September 2017; Published: 8 September 2017 Abstract: Quantitative phase analyses of carbonate rocks containing Mg-rich calcite and non- stoichiometric dolomite by the Rietveld method yielded improved results when the substitutions are refined for either minerals. The refinement is constrained by the c-axis of the lattice for both minerals using the formula c = −1.8603 nMg + 17.061 for calcite, where nMg is the molar fraction of Mg replacing Ca, and c = 16.0032 + 0.8632ΔnCa for dolomite, with ΔnCa being the excess Ca in its B site. The one-step procedure was implemented into the Topas software and tested on twenty-two carbonate rock samples from diverse geological settings, considered analogues to petroleum system lithotypes of the pre-evaporite deposits of Southeastern Brazil. The case study spans over a wide range of calcite and dolomite compositions: up to 0.287 apfu Mg in magnesian calcite, and Ca in excess of up to 0.25 apfu in non-stoichiometric dolomite, which are maximum substitutions the formulas support. The method overcomes the limitations for the quantification of minerals by stoichiometry based on whole-rock chemical analysis for complex mineralogy and can be employed for multiple generations of either carbonate. -
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. -
Definition of Chalk
1.1: Introduction: 1.1.1: Definition of chalk: Chalk is a soft, white, porous sedimentary carbonate rock, a form of limestone composed of the mineral calcite. Calcite is calcium carbonate or CaCO3. It forms under reasonably deep marine conditions from the gradual accumulation of minute calcite shells (coccoliths) shed from micro-organisms called coccolithophores. Flint (a type of chert unique to chalk) is very common as bands parallel to the bedding or as nodules embedded in chalk. It is probably derived from sponge spicules or other siliceous organisms as water is expelled upwards during compaction. Flint is often deposited around larger fossils such as Echinoidea which may be silicified (i.e. replaced molecule by molecule by flint). Chalk as seen in Cretaceous deposits of Western Europe is unusual among sedimentary limestone in the thickness of the beds. Most cliffs of chalk have very few obvious bedding planes unlike most thick sequences of limestone such as the Carboniferous Limestone or the Jurassic oolitic limestones. This presumably indicates very stable conditions over tens of millions of years. Figure (1-1): Calcium sulphate 1 "Nitzana Chalk curves" situated at Western Negev, Israel are chalk deposits formed at the Mesozoic era's Tethys Ocean Chalk has greater resistance to weathering and slumping than the clays with which it is usually associated, thus forming tall steep cliffs where chalk ridges meet the sea. Chalk hills, known as chalk downland, usually form where bands of chalk reach the surface at an angle, so forming a scarp slope. Because chalk is well jointed it can hold a large volume of ground water, providing a natural reservoir that releases water slowly through dry seasons. -
Influence of Boulder Concentration on Turbulence and Sediment
PUBLICATIONS Journal of Geophysical Research: Earth Surface RESEARCH ARTICLE Influence of Boulder Concentration on Turbulence 10.1002/2017JF004221 and Sediment Transport in Open-Channel Flow Key Points: Over Submerged Boulders • The presence of large immobile boulders significantly influences the H. W. Fang1, Y. Liu1, and T. Stoesser2 flow and turbulence field in the vicinity of submerged boulders 1Department of Hydraulic Engineering, Tsinghua University, Beijing, China, 2School of Civil Engineering, Cardiff University, • The boulder concentration plays an important role in forming skimming to Cardiff, UK isolated roughness flows and predicting bed load transport rates • The bed load transport rate will be Abstract In this paper the effects of boulder concentration on hydrodynamics and local and underestimated when using the reach-averaged sediment transport properties with a flow over submerged boulder arrays are investigated. reach-averaged shear stress, ’ compared with that based on local Four numerical simulations are performed in which the boulders streamwise spacings are varied. Statistics shear stress of near-bed velocity, Reynolds shear stresses, and turbulent events are collected and used to predict bed load transport rates. The results demonstrate that the presence of boulders at various interboulder spacings fl fi fl Supporting Information: altered the ow eld in their vicinity causing (1) ow deceleration, wake formation, and vortex shedding; • Supporting Information S1 (2) enhanced outward and inward interaction turbulence events downstream of the boulders; and (3) a • Movie S1 redistribution of the local bed shear stress around the boulder consisting of pockets of high and low bed shear stresses. The spatial variety of the predicted bed load transport rate qs based on local bed shear stress is Correspondence to: Y. -
Oregon Department of Human Services HEALTH EFFECTS INFORMATION
Oregon Department of Human Services Office of Environmental Public Health (503) 731-4030 Emergency 800 NE Oregon Street #604 (971) 673-0405 Portland, OR 97232-2162 (971) 673-0457 FAX (971) 673-0372 TTY-Nonvoice TECHNICAL BULLETIN HEALTH EFFECTS INFORMATION Prepared by: Department of Human Services ENVIRONMENTAL TOXICOLOGY SECTION Office of Environmental Public Health OCTOBER, 1998 CALCIUM CARBONATE "lime, limewater” For More Information Contact: Environmental Toxicology Section (971) 673-0440 Drinking Water Section (971) 673-0405 Technical Bulletin - Health Effects Information CALCIUM CARBONATE, "lime, limewater@ Page 2 SYNONYMS: Lime, ground limestone, dolomite, sugar lime, oyster shell, coral shell, marble dust, calcite, whiting, marl dust, putty dust CHEMICAL AND PHYSICAL PROPERTIES: - Molecular Formula: CaCO3 - White solid, crystals or powder, may draw moisture from the air and become damp on exposure - Odorless, chalky, flat, sweetish flavor (Do not confuse with "anhydrous lime" which is a special form of calcium hydroxide, an extremely caustic, dangerous product. Direct contact with it is immediately injurious to skin, eyes, intestinal tract and respiratory system.) WHERE DOES CALCIUM CARBONATE COME FROM? Calcium carbonate can be mined from the earth in solid form or it may be extracted from seawater or other brines by industrial processes. Natural shells, bones and chalk are composed predominantly of calcium carbonate. WHAT ARE THE PRINCIPLE USES OF CALCIUM CARBONATE? Calcium carbonate is an important ingredient of many household products. It is used as a whitening agent in paints, soaps, art products, paper, polishes, putty products and cement. It is used as a filler and whitener in many cosmetic products including mouth washes, creams, pastes, powders and lotions. -
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. -
Source to Surface Model of Monogenetic Volcanism: a Critical Review
Downloaded from http://sp.lyellcollection.org/ by guest on September 28, 2021 Source to surface model of monogenetic volcanism: a critical review I. E. M. SMITH1 &K.NE´ METH2* 1School of Environment, University of Auckland, Auckland, New Zealand 2Volcanic Risk Solutions, Massey University, Palmerston North 4442, New Zealand *Correspondence: [email protected] Abstract: Small-scale volcanic systems are the most widespread type of volcanism on Earth and occur in all of the main tectonic settings. Most commonly, these systems erupt basaltic magmas within a wide compositional range from strongly silica undersaturated to saturated and oversatu- rated; less commonly, the spectrum includes more siliceous compositions. Small-scale volcanic systems are commonly monogenetic in the sense that they are represented at the Earth’s surface by fields of small volcanoes, each the product of a temporally restricted eruption of a composition- ally distinct batch of magma, and this is in contrast to polygenetic systems characterized by rela- tively large edifices built by multiple eruptions over longer periods of time involving magmas with diverse origins. Eruption styles of small-scale volcanoes range from pyroclastic to effusive, and are strongly controlled by the relative influence of the characteristics of the magmatic system and the surface environment. Gold Open Access: This article is published under the terms of the CC-BY 3.0 license. Small-scale basaltic magmatic systems characteris- hazards associated with eruptions, and this is tically occur at the Earth’s surface as fields of small particularly true where volcanic fields are in close monogenetic volcanoes. These volcanoes are the proximity to population centres.