The Middle-Upper Ordovician Simpson Group of the Permian Basin: Deposition, Diagenesis, and Reservoir Development
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Paleontological Contributions Number 18 Efficient Ornamentation in Ordovician Anthaspidellid Sponges Stephen B. Church August 9, 2017 Lawrence, Kansas, USA ISSN 1946-0279 (online) paleo.ku.edu/contributions Ridge-and-trough ornamented outer-wall fragment of the Ordovician anthaspidellid sponge Rugocoelia eganensis Johns, 1994. Paleontological Contributions August 9, 2017 Number 18 EFFICIENT ORNAMENTATION IN ORDOVICIAN ANTHASPIDELLID SPONGES Stephen B. Church Department of Geological Sciences, Brigham Young University, Provo, Utah 84602-3300, [email protected] ABSTRACT Lithistid orchoclad sponges within the family Anthaspidellidae Ulrich in Miller, 1889 include several genera that added ornate features to their outer-wall surfaces during Early Ordovician sponge radiation. Ornamented anthaspidellid sponges commonly constructed annulated or irregularly to regularly spaced transverse ridge-and-trough features on their outer-wall surfaces without proportionately increasing the size of their internal wall or gastral surfaces. This efficient technique of modi- fying only the sponge’s outer surface without enlarging its entire skeletal frame conserved the sponge’s constructional energy while increasing outer-wall surface-to-fluid exposure for greater intake of nutrient bearing currents. Sponges with widely spaced ridge-and-trough ornament dimensions predominated in high-energy settings. Widely spaced ridges and troughs may have given the sponge hydrodynamic benefits in high wave force settings. Ornamented sponges with narrowly spaced ridge-and- trough dimensions are found in high energy paleoenvironments but also occupied moderate to low-energy settings, where their surface-to-fluid exposure per unit area exceeded that of sponges with widely spaced surface ornamentations. Keywords: lithistid sponges, Ordovician radiation, morphological variation, theoretical morphology INTRODUCTION assumed by most anthaspidellids. -
Cambrian Ordovician
Open File Report LXXVI the shale is also variously colored. Glauconite is generally abundant in the formation. The Eau Claire A Summary of the Stratigraphy of the increases in thickness southward in the Southern Peninsula of Michigan where it becomes much more Southern Peninsula of Michigan * dolomitic. by: The Dresbach sandstone is a fine to medium grained E. J. Baltrusaites, C. K. Clark, G. V. Cohee, R. P. Grant sandstone with well rounded and angular quartz grains. W. A. Kelly, K. K. Landes, G. D. Lindberg and R. B. Thin beds of argillaceous dolomite may occur locally in Newcombe of the Michigan Geological Society * the sandstone. It is about 100 feet thick in the Southern Peninsula of Michigan but is absent in Northern Indiana. The Franconia sandstone is a fine to medium grained Cambrian glauconitic and dolomitic sandstone. It is from 10 to 20 Cambrian rocks in the Southern Peninsula of Michigan feet thick where present in the Southern Peninsula. consist of sandstone, dolomite, and some shale. These * See last page rocks, Lake Superior sandstone, which are of Upper Cambrian age overlie pre-Cambrian rocks and are The Trempealeau is predominantly a buff to light brown divided into the Jacobsville sandstone overlain by the dolomite with a minor amount of sandy, glauconitic Munising. The Munising sandstone at the north is dolomite and dolomitic shale in the basal part. Zones of divided southward into the following formations in sandy dolomite are in the Trempealeau in addition to the ascending order: Mount Simon, Eau Claire, Dresbach basal part. A small amount of chert may be found in and Franconia sandstones overlain by the Trampealeau various places in the formation. -
Chapter 2 Paleozoic Stratigraphy of the Grand Canyon
CHAPTER 2 PALEOZOIC STRATIGRAPHY OF THE GRAND CANYON PAIGE KERCHER INTRODUCTION The Paleozoic Era of the Phanerozoic Eon is defined as the time between 542 and 251 million years before the present (ICS 2010). The Paleozoic Era began with the evolution of most major animal phyla present today, sparked by the novel adaptation of skeletal hard parts. Organisms continued to diversify throughout the Paleozoic into increasingly adaptive and complex life forms, including the first vertebrates, terrestrial plants and animals, forests and seed plants, reptiles, and flying insects. Vast coal swamps covered much of mid- to low-latitude continental environments in the late Paleozoic as the supercontinent Pangaea began to amalgamate. The hardiest taxa survived the multiple global glaciations and mass extinctions that have come to define major time boundaries of this era. Paleozoic North America existed primarily at mid to low latitudes and experienced multiple major orogenies and continental collisions. For much of the Paleozoic, North America’s southwestern margin ran through Nevada and Arizona – California did not yet exist (Appendix B). The flat-lying Paleozoic rocks of the Grand Canyon, though incomplete, form a record of a continental margin repeatedly inundated and vacated by shallow seas (Appendix A). IMPORTANT STRATIGRAPHIC PRINCIPLES AND CONCEPTS • Principle of Original Horizontality – In most cases, depositional processes produce flat-lying sedimentary layers. Notable exceptions include blanketing ash sheets, and cross-stratification developed on sloped surfaces. • Principle of Superposition – In an undisturbed sequence, older strata lie below younger strata; a package of sedimentary layers youngs upward. • Principle of Lateral Continuity – A layer of sediment extends laterally in all directions until it naturally pinches out or abuts the walls of its confining basin. -
The Geologic Time Scale Is the Eon
Exploring Geologic Time Poster Illustrated Teacher's Guide #35-1145 Paper #35-1146 Laminated Background Geologic Time Scale Basics The history of the Earth covers a vast expanse of time, so scientists divide it into smaller sections that are associ- ated with particular events that have occurred in the past.The approximate time range of each time span is shown on the poster.The largest time span of the geologic time scale is the eon. It is an indefinitely long period of time that contains at least two eras. Geologic time is divided into two eons.The more ancient eon is called the Precambrian, and the more recent is the Phanerozoic. Each eon is subdivided into smaller spans called eras.The Precambrian eon is divided from most ancient into the Hadean era, Archean era, and Proterozoic era. See Figure 1. Precambrian Eon Proterozoic Era 2500 - 550 million years ago Archaean Era 3800 - 2500 million years ago Hadean Era 4600 - 3800 million years ago Figure 1. Eras of the Precambrian Eon Single-celled and simple multicelled organisms first developed during the Precambrian eon. There are many fos- sils from this time because the sea-dwelling creatures were trapped in sediments and preserved. The Phanerozoic eon is subdivided into three eras – the Paleozoic era, Mesozoic era, and Cenozoic era. An era is often divided into several smaller time spans called periods. For example, the Paleozoic era is divided into the Cambrian, Ordovician, Silurian, Devonian, Carboniferous,and Permian periods. Paleozoic Era Permian Period 300 - 250 million years ago Carboniferous Period 350 - 300 million years ago Devonian Period 400 - 350 million years ago Silurian Period 450 - 400 million years ago Ordovician Period 500 - 450 million years ago Cambrian Period 550 - 500 million years ago Figure 2. -
PUBLICATIONS by JAMES SPRINKLE 1965 -- Sprinkle, James
PUBLICATIONS BY JAMES SPRINKLE 1965 -- Sprinkle, James. 1965. Stratigraphy and sedimentary petrology of the lower Lodgepole Formation of southwestern Montana. M.I.T. Department of Geology and Geophysics, unpublished Senior Thesis, 29 p. (see #56 and 66 below) 1966 1. Sprinkle, James and Gutschick, R. C. 1966. Blastoids from the Sappington Formation of southwest Montana (Abst.). Geological Society of America Special Paper 87:163-164. 1967 2. Sprinkle, James and Gutschick, R. C. 1967. Costatoblastus, a channel fill blastoid from the Sappington Formation of Montana. Journal of Paleon- tology, 41(2):385-402. 1968 3. Sprinkle, James. 1968. The "arms" of Caryocrinites, a Silurian rhombiferan cystoid (Abst.). Geological Society of America Special Paper 115:210. 1969 4. Sprinkle, James. 1969. The early evolution of crinozoan and blastozoan echinoderms (Abst.). Geological Society of America Special Paper 121:287-288. 5. Robison, R. A. and Sprinkle, James. 1969. A new echinoderm from the Middle Cambrian of Utah (Abst.). Geological Society of America Abstracts with Programs, 1(5):69. 6. Robison, R. A. and Sprinkle, James. 1969. Ctenocystoidea: new class of primitive echinoderms. Science, 166(3912):1512-1514. 1970 -- Sprinkle, James. 1970. Morphology and Evolution of Blastozoan Echino- derms. Harvard University Department of Geological Sciences, unpublished Ph.D. Thesis, 433 p. (see #8 below) 1971 7. Sprinkle, James. 1971. Stratigraphic distribution of echinoderm plates in the Antelope Valley Limestone of Nevada and California. U.S. Geological Survey Professional Paper 750-D (Geological Survey Research 1971):D89-D98. 1973 8. Sprinkle, James. 1973. Morphology and Evolution of Blastozoan Echino- derms. Harvard University, Museum of Comparative Zoology Special Publication, 283 p. -
Chordates (Phylum Chordata)
A short story Leathem Mehaffey, III, Fall 201993 The First Chordates (Phylum Chordata) • Chordates (our phylum) first appeared in the Cambrian, 525MYA. 94 Invertebrates, Chordates and Vertebrates • Invertebrates are all animals not chordates • Generally invertebrates, if they have hearts, have dorsal hearts; if they have a nervous system it is usually ventral. • All vertebrates are chordates, but not all chordates are vertebrates. • Chordates: • Dorsal notochord • Dorsal nerve chord • Ventral heart • Post-anal tail • Vertebrates: Amphioxus: archetypal chordate • Dorsal spinal column (articulated) and skeleton 95 Origin of the Chordates 96 Haikouichthys Myllokunmingia Note the rounded extension to Possibly the oldest the head bearing sensory vertebrate: showed gill organs bars and primitive vertebral elements Early and primitive agnathan vertebrates of the Early Cambrian (530MYA) Pikaia Note: these organisms were less Primitive chordate, than an inch long. similar to Amphioxus 97 The Cambrian/Ordovician Extinction • Somewhere around 488 million years ago something happened to cause a change in the fauna of the earth, heralding the beginning of the Ordovician Period. • Rather than one catastrophe, the late-Cambrian extinction seems to be a series of smaller extinction events. • Historically the change in fauna (mostly trilobites as the index species) was thought to be due to excessive warmth and low oxygen. • But some current findings point to an oxygen spike due perhaps to continental drift into the tropics, driving rapid speciation and consequent replacement of old with new organisms. 98 Welcome to the Ordovician YOU ARE HERE 99 The Ordovician Sea, 488 million years 100 ago The Ordovician Period lasted almost 45 million years, from 489 to 444 MYA. -
Distribution of the Middle Ordovician Copenhagen Formation and Its Trilobites in Nevada
Distribution of the Middle Ordovician Copenhagen Formation and its Trilobites in Nevada GEOLOGICAL SURVEY PROFESSIONAL PAPER 749 Distribution of the Middle Ordovician Copenhagen Formation and its Trilobites in Nevada By REUBEN JAMES ROSS, JR., and FREDERICK C. SHAW GEOLOGICAL SURVEY PROFESSIONAL PAPER 749 Descriptions of Middle Ordovician trilobites belonging to 21 genera contribute to correlations between similar strata in Nevada) California) and 0 klahoma UNITED STATES GOVERNMENT PRINTING OFFICE, WASHINGTON 1972 UNITED STATES DEPARTMENT OF THE INTERIOR ROGERS C. B. lVIOR TON, Secretary GEOLOGICAL SURVEY V. E. McKelvey, Director Library of Congress catalog-card No. 78-190301 For sale by the Superintendent of Documents, U.S. Government Printing Office Washington, D.C. 20402 - Price 70 cents (paper cover) Stock Number 2401-2109 CONTENTS Page Page Abstract ______________________________ -------------------------------------------------- 1 Descriptions of trilobites __________________________________________________ _ 14 Introduction ________________________________________________________________________ _ 1 Genus T1·iarth1·us Green, 1832 .... ------------------------------ 14 Previous investigations _____________________________________________ _ 1 Genus Carrickia Tripp, 1965 ____________________________________ _ 14 Acknowledgments-------------------------------------------------------· 1 Genus Hypodicranotus Whittington, 1952 _____________ _ 15 Geographic occurrences of the Copenhagen Genus Robergia Wiman, 1905·---------------------------------- -
Reinterpretation of the Enigmatic Ordovician Genus Bolboporites (Echinodermata)
Reinterpretation of the enigmatic Ordovician genus Bolboporites (Echinodermata). Emeric Gillet, Bertrand Lefebvre, Véronique Gardien, Emilie Steimetz, Christophe Durlet, Frédéric Marin To cite this version: Emeric Gillet, Bertrand Lefebvre, Véronique Gardien, Emilie Steimetz, Christophe Durlet, et al.. Reinterpretation of the enigmatic Ordovician genus Bolboporites (Echinodermata).. Zoosymposia, Magnolia Press, 2019, 15 (1), pp.44-70. 10.11646/zoosymposia.15.1.7. hal-02333918 HAL Id: hal-02333918 https://hal.archives-ouvertes.fr/hal-02333918 Submitted on 13 Nov 2020 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. 1 Reinterpretation of the Enigmatic Ordovician Genus Bolboporites 2 (Echinodermata) 3 4 EMERIC GILLET1, BERTRAND LEFEBVRE1,3, VERONIQUE GARDIEN1, EMILIE 5 STEIMETZ2, CHRISTOPHE DURLET2 & FREDERIC MARIN2 6 7 1 Université de Lyon, UCBL, ENSL, CNRS, UMR 5276 LGL-TPE, 2 rue Raphaël Dubois, F- 8 69622 Villeurbanne, France 9 2 Université de Bourgogne - Franche Comté, CNRS, UMR 6282 Biogéosciences, 6 boulevard 10 Gabriel, F-2100 Dijon, France 11 3 Corresponding author, E-mail: [email protected] 12 13 Abstract 14 Bolboporites is an enigmatic Ordovician cone-shaped fossil, the precise nature and systematic affinities of 15 which have been controversial over almost two centuries. -
Proterozoic Paleozoic Cambrian Ordovician Silurian Devonian
Approximate location of Burley No. 1 well Seismic Stratigraphic Extensional and Thrust Age West Formation or Group Name East Lithology Packages Orogenic Events Sheets Perm. Lower Upper Post-Pottsville rocks, undivided Pottsville Group and Middle post-Pottsville rocks Alleghanian orogeny Penn. Lower Pottsville Group Upper Greenbrier Limestone and Mauch Chunk Group Greenbrier Limestone Miss. Lower Berea Sandstone, Sunbury Shale, and Price Formation Venango Group Venango Group (Formation) Hampshire Formation and Riceville Formation Chagrin Shale Bradford Group Bradford Group Huron Mbr. of Greenland Gap Group the Ohio Shale Upper Salina sheet Acadian orogeny Java Formation Angola Shale Member Devonian West Falls Elk Group Formation Rhinestreet Shale Member Brallier Formation Elk Group Sonyea Formation Genesee Formation Harrell Shale Middle Tully Limestone, Hamilton Group, Marcellus Shale, and Onondaga Limestone Hamilton Group Lower Oriskany Sandstone and Helderberg Group Upper Salina Group (includes salt beds) Salina Group, Tonoloway Limestone, and Wills Creek Formation and Wills Creek Formation Salina Group Paleozoic Lockport Dolomite and Keefer Sandstone McKenzie Limestone and Keefer Sandstone Silurian Rose Hill Formation Lower Reedsville- Tuscarora Sandstone Taconic orogeny Martinsburg Juniata Formation Juniata Formation sheet Oswego Sandstone Upper Reedsville Shale (Utica Shale at base) Reedsville Shale Trenton Limestone Trenton Limestone Black River Limestone Middle Ordovician Knox unconformity Beekmantown Group Beekmantown Group ? Passive continental Lower Rome- margin modified Waynesboro Upper sandstone member of the Copper Ridge Dolomite of the Knox Group by Rome trough sheet Upper extension Copper Ridge Dolomite of the Knox Group Knox Group and Middle pre-Knox rocks Conasauga Group and Rome Formation Cambrian Lower Autochthonous Grenvillian basement Grenvillian Grenvillian basement basement Proterozoic Figure 3.--Correlation chart of Paleozoic and Proterozoic rocks in the study area and associated thrust sheets. -
Estimating Dispersal and Evolutionary Dynamics in Diploporan Blastozoans (Echinodermata) Across the Great Ordovician Biodiversification Ve Ent
University of South Florida Scholar Commons School of Geosciences Faculty and Staff Publications School of Geosciences 2020 Estimating Dispersal and Evolutionary Dynamics in Diploporan Blastozoans (Echinodermata) Across the Great Ordovician Biodiversification vE ent Adriane R. Lam University of Massachusetts Sarah L. Sheffield University of South Florida, [email protected] Nicholas J. Matzke University of Auckland Follow this and additional works at: https://scholarcommons.usf.edu/geo_facpub Part of the Earth Sciences Commons Scholar Commons Citation Lam, Adriane R.; Sheffield, Sarah L.; and Matzke, Nicholas J., "Estimating Dispersal and Evolutionary Dynamics in Diploporan Blastozoans (Echinodermata) Across the Great Ordovician Biodiversification Event" (2020). School of Geosciences Faculty and Staff Publications. 2291. https://scholarcommons.usf.edu/geo_facpub/2291 This Article is brought to you for free and open access by the School of Geosciences at Scholar Commons. It has been accepted for inclusion in School of Geosciences Faculty and Staff Publications by an authorized administrator of Scholar Commons. For more information, please contact [email protected]. Paleobiology, 2020, pp. 1–23 DOI: 10.1017/pab.2020.24 Article Estimating dispersal and evolutionary dynamics in diploporan blastozoans (Echinodermata) across the great Ordovician biodiversification event Adriane R. Lam†, Sarah L. Sheffield† , and Nicholas J. Matzke Abstract.—Echinoderms make up a substantial component of Ordovician marine invertebrates, yet their speciation and dispersal history as inferred within a rigorous phylogenetic and statistical framework is lacking. We use biogeographic stochastic mapping (BSM; implemented in the R package BioGeoBEARS) to infer ancestral area relationships and the number and type of dispersal events through the Ordovician for diploporan blastozoans and related species. -
Thesis-2002-F832d.Pdf
THE DEPOSITIONAL HISTORY OF THE SYCAMOREL~STONE By KAREN ELIZABETH FRANKLIN Bachelor ofScience Oklahoma State University Stillwater, Oklahoma 1997 Submitted to the faculty ofthe Graduate College of Oklahoma State University in partial fulfillment of the requirements for the Degree of MASTER OF SCIENCE August, 2002 THE DEPOSITIONAL HISTORY OF THE SYCAMORE LIMESTONE Thesis Approved: Thesis Adviser 11 ACKNOWLEDGEMENTS I sincerely thank my advisers for all their help and patience with this thesis. Dr. Al Shaieb provided me with confidence and an unending supply of information. Dr. Boardman and Dr. Cemen provided helpful information from their disciplines. I thank my parents for all their help as well. They supported my family and I both mentally and financially. I especially thank Mom and Dad for watching my sons when I just had to get to school to work. I cannot express how thankful I am to my husband for all his support while I was working on my thesis. Without him, this wouldn't be possible. He and my sons provided support and love when things didn't seem to be going right. Finally I would like to thank the professors in the Geology Department and my fellow students for suffering through my constant questions. Many of them provided ideas and answers that helped me continue on those days where it seemed impossible to do so. III TABLE OF CONTENTS Chapter Page I. INTRODUCTION 1 Purpose ofStudy 1 Location 1 Method ofStudy 3 Formation History 3 Previous Investigations 6 II. GEOLOGICAL SETTING 13 Regional Structure 13 Regional Stratigraphy 16 Sequence Stratigraphy 20 III. -
A New Family of Trepostome Bryozoans from the Ordovician Simpson Group of Oklahoma
700 JOURNAL OF PALEONTOLOGY, V. 64, NO. 5, 1990 --, B. D. PRATI, AND A. J. ROWELL. 1989. Early Cambrian reefs, Holyoake Range, Antarctica. New Zealand Journal of Geology and reef complexes, and associated lithofacies of the Shackleton Lime Geophysics, 31:397-404. stone, Transantarctic Mountains. Sedimentology, 36:341-362. Sowv'Ev, I. A., AND G. E. GRIKUROV. 1979. Novie dannie o ras --, AND A. J. ROWELL. In press. The pre-Devonian Palaeozoic elas prostranenii Kembriyskikh trilobitov v khrebtakh Ardzhentina i She tics of the central Transantarctic Mountains: stratigraphy and depo klton [New data on the spread of Cambrian trilobites in the Argentina sitional setting. In M. R. A. Thomson, J. W. Crame, and J. W. Thom and Shackleton Mountains]. Antarktika, 18:54-73. son (eds.), Geologic Evolution of Antarctica. Cambridge University TATE, R. 1892. The Cambrian fossils ofSouth Australia. Transactions Press, Cambridge. and Proceedings of the Royal Society of South Australia, 15:183- ROWELL, A. J., K. R. EvANs, AND M. N. REES. 1989. Fauna of the 189. Shackleton Limestone. Antarctic Journal of the United States, 1988 WRONA, R. 1987. Cambrian microfossil Hadimopanel/a Gedik from Review, 23(5):13-14. glacial erratics in West Antarctica. Palaeontological Polonica, 49:37- --, AND M. N. REES. 1989. Early Palaeozoic history of the upper 48. Beardmore Glacier area: implications for a major Antarctic structural Y OCHELSON, E. L. AND E. STUMP. 1977. Discovery of Early Cambrian boundary within the Transantarctic Mountains. Antarctic Science, l: fossils at Taylor Nunatak, Antarctica. Journal of Paleontology, 81: 249-260. 872-875. --, --, R. A. COOPER, AND B. R.