28. Late Jurassic–Early Cretaceous
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Stratigraphy and Paleontology of Mid-Cretaceous Rocks in Minnesota and Contiguous Areas
Stratigraphy and Paleontology of Mid-Cretaceous Rocks in Minnesota and Contiguous Areas GEOLOGICAL SURVEY PROFESSIONAL PAPER 1253 Stratigraphy and Paleontology of Mid-Cretaceous Rocks in Minnesota and Contiguous Areas By WILLIAM A. COBBAN and E. A. MEREWETHER Molluscan Fossil Record from the Northeastern Part of the Upper Cretaceous Seaway, Western Interior By WILLIAM A. COBBAN Lower Upper Cretaceous Strata in Minnesota and Adjacent Areas-Time-Stratigraphic Correlations. and Structural Attitudes By E. A. M EREWETHER GEOLOGICAL SURVEY PROFESSIONAL PAPER 1 2 53 UNITED STATES GOVERNMENT PRINTING OFFICE, WASHINGTON 1983 UNITED STATES DEPARTMENT OF THE INTERIOR JAMES G. WATT, Secretary GEOLOGICAL SURVEY Dallas L. Peck, Director Library of Congress Cataloging in Publication Data Cobban, William Aubrey, 1916 Stratigraphy and paleontology of mid-Cretaceous rocks in Minnesota and contiguous areas. (Geological Survey Professional Paper 1253) Bibliography: 52 p. Supt. of Docs. no.: I 19.16 A. Molluscan fossil record from the northeastern part of the Upper Cretaceous seaway, Western Interior by William A. Cobban. B. Lower Upper Cretaceous strata in Minnesota and adjacent areas-time-stratigraphic correlations and structural attitudes by E. A. Merewether. I. Mollusks, Fossil-Middle West. 2. Geology, Stratigraphic-Cretaceous. 3. Geology-Middle West. 4. Paleontology-Cretaceous. 5. Paleontology-Middle West. I. Merewether, E. A. (Edward Allen), 1930. II. Title. III. Series. QE687.C6 551.7'7'09776 81--607803 AACR2 For sale by the Distribution Branch, U.S. -
Fossil Polychaetes from the Upper Cretaceous Rock Formations of South India—
FOSSIL POLYCHAETES FROM THE UPPER CRETACEOUS ROCK FORMATIONS OF SOUTH INDIA--PART II BY G. W. CHIPLONKAR AND P. M. TAPASWI (Maharashtra Association for the Cultivation of Science, Poona-4) Received October 29, 1972 (Communicated by Prof. T.S. Mahabale) ABSTRACT Eight polychaetan species are described here, three of which, viz., Burtinella concava (Sow.), Tubulostium eallosum Stol. T. discoidium Stol., described by Stoliczka as gastropod species, are now transferred to the Polyehaeta in the light of new information. Among the three species described here as new to science, one has for its proper placement, necessitated creation of the now genus, viz., Rotulispira falling under the subfamily Spirorbinae Chamborlin. Spirorbula Nielsen is repotted for the first time from South Indian Cretaceous. Family Terebellidae Grube represented by Terebellolites Desio, a heterogenous group, is also recorded for the first time from these deposits. INTRODUCTION IN the present communication eight more (Chiplonkar and Tapaswi, 1973, Pt. I) polychaetan species are described. As mentioned in Part I, we have followed, except where otherwise indicated, Regenhardt (1961) in his classification of the Serpulidae. CO-ORDINATES OF LOCALITIES CITED IN THE TEXT (1) Ariyalur 11 ° 07' 30" : 79 ° 04' 30", (2) Kallankurichchi 11° 09' : 79 ° 07' 30", (3) Mallur 11 ° 04' 30" : 79 ° 05', (4) Mettal 11 ° 05' 40" : 79 ° 00' 30", (5) Naicolum 11 ° 03' 30" : 78 ° 50' 30", (6) Odiyam 11 ° 13' : 78 ° 59"30", (7) Pondicherry 11 ° 56' : 79 ° 50', (8) Saradamangalam 11 ° 03' 30" : 78 ° 57', (9) Sillakkudi 11° 04' 30" : 79 ° 00' 30", (10) Uttattur 1! ° 04' : 78 ° 51', 202 The Upper Cretaceous Rock Formations of South IndiamH 203 ACKNOWLEDGEMENTS Dr. -
Triassic- Jurassic Stratigraphy Of
Triassic- Jurassic Stratigraphy of the <JF C7 JL / Culpfeper and B arbour sville Basins, VirginiaC7 and Maryland/ ll.S. PAPER Triassic-Jurassic Stratigraphy of the Culpeper and Barboursville Basins, Virginia and Maryland By K.Y. LEE and AJ. FROELICH U.S. GEOLOGICAL SURVEY PROFESSIONAL PAPER 1472 A clarification of the Triassic--Jurassic stratigraphic sequences, sedimentation, and depositional environments UNITED STATES GOVERNMENT PRINTING OFFICE, WASHINGTON: 1989 DEPARTMENT OF THE INTERIOR MANUEL LUJAN, Jr., Secretary U.S. GEOLOGICAL SURVEY Dallas L. Peck, Director Any use of trade, product, or firm names in this publication is for descriptive purposes only and does not imply endorsement by the U.S. Government Library of Congress Cataloging in Publication Data Lee, K.Y. Triassic-Jurassic stratigraphy of the Culpeper and Barboursville basins, Virginia and Maryland. (U.S. Geological Survey professional paper ; 1472) Bibliography: p. Supt. of Docs. no. : I 19.16:1472 1. Geology, Stratigraphic Triassic. 2. Geology, Stratigraphic Jurassic. 3. Geology Culpeper Basin (Va. and Md.) 4. Geology Virginia Barboursville Basin. I. Froelich, A.J. (Albert Joseph), 1929- II. Title. III. Series. QE676.L44 1989 551.7'62'09755 87-600318 For sale by the Books and Open-File Reports Section, U.S. Geological Survey, Federal Center, Box 25425, Denver, CO 80225 CONTENTS Page Page Abstract.......................................................................................................... 1 Stratigraphy Continued Introduction... .......................................................................................... -
Phylogenetic Relationships of Serpulidae (Annelida: Polychaeta) Based on 18S Rdna Sequence Data, and Implications for Opercular Evolution Janina Lehrkea,Ã, Harry A
ARTICLE IN PRESS Organisms, Diversity & Evolution 7 (2007) 195–206 www.elsevier.de/ode Phylogenetic relationships of Serpulidae (Annelida: Polychaeta) based on 18S rDNA sequence data, and implications for opercular evolution Janina Lehrkea,Ã, Harry A. ten Hoveb, Tara A. Macdonaldc, Thomas Bartolomaeusa, Christoph Bleidorna,1 aInstitute for Zoology, Animal Systematics and Evolution, Freie Universitaet Berlin, Koenigin-Luise-Street 1-3, 14195 Berlin, Germany bZoological Museum, University of Amsterdam, P.O. Box 94766, 1090 GT Amsterdam, The Netherlands cBamfield Marine Sciences Centre, Bamfield, British Columbia, Canada, V0R 1B0 Received 19 December 2005; accepted 2 June 2006 Abstract Phylogenetic relationships of (19) serpulid taxa (including Spirorbinae) were reconstructed based on 18S rRNA gene sequence data. Maximum likelihood, Bayesian inference, and maximum parsimony methods were used in phylogenetic reconstruction. Regardless of the method used, monophyly of Serpulidae is confirmed and four monophyletic, well- supported major clades are recovered: the Spirorbinae and three groups hitherto referred to as the Protula-, Serpula-, and Pomatoceros-group. Contrary to the taxonomic literature and the hypothesis of opercular evolution, the Protula- clade contains non-operculate (Protula, Salmacina) and operculate taxa both with pinnulate and non-pinnulate peduncle (Filograna vs. Vermiliopsis), and most likely is the sister group to Spirorbinae. Operculate Serpulinae and poorly or non-operculate Filograninae are paraphyletic. It is likely that lack of opercula in some serpulid genera is not a plesiomorphic character state, but reflects a special adaptation. r 2007 Gesellschaft fu¨r Biologische Systematik. Published by Elsevier GmbH. All rights reserved. Keywords: Serpulidae; Phylogeny; Operculum; 18S rRNA gene; Annelida; Polychaeta Introduction distinctive calcareous tubes and bilobed tentacular crowns, each with numerous radioles that bear shorter Serpulids are common members of marine hard- secondary branches (pinnules) on the inner side. -
Biomineralization of Polychaete Annelids in the Fossil Record
minerals Review Biomineralization of Polychaete Annelids in the Fossil Record Olev Vinn Department of Geology, University of Tartu, Ravila 14A, 50411 Tartu, Estonia; [email protected]; Tel.: +372-5067728 Received: 31 August 2020; Accepted: 25 September 2020; Published: 29 September 2020 Abstract: Ten distinct microstructures occur in fossil serpulids and serpulid tubes can contain several layers with different microstructures. Diversity and complexity of serpulid skeletal structures has greatly increased throughout their evolution. In general, Cenozoic serpulid skeletal structures are better preserved than Mesozoic ones. The first complex serpulid microstructures comparable to those of complex structures of molluscs appeared in the Eocene. The evolution of serpulid tube microstructures can be explained by the importance of calcareous tubes for serpulids as protection against predators and environmental disturbances. Both fossil cirratulids and sabellids are single layered and have only spherulitic prismatic tube microstructures. Microstructures of sabellids and cirratulids have not evolved since the appearance of calcareous species in the Jurassic and Oligocene, respectively. The lack of evolution in sabellids and cirratulids may result from the unimportance of biomineralization for these groups as only few species of sabellids and cirratulids have ever built calcareous tubes. Keywords: biominerals; calcite; aragonite; skeletal structures; serpulids; sabellids; cirratulids; evolution 1. Introduction Among polychaete annelids, calcareous tubes are known in serpulids, cirratulids and sabellids [1–3]. The earliest serpulids and sabellids are known from the Permian [4], and cirratulids from the Oligocene [5]. Only serpulids dwell exclusively within calcareous tubes. Polychaete annelids build their tubes from calcite, aragonite or a mixture of both polymorphs. Calcareous polychaete tubes possess a variety of ultrastructural fabrics, from simple to complex, some being unique to annelids [1]. -
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. -
The Late Jurassic Tithonian, a Greenhouse Phase in the Middle Jurassic–Early Cretaceous ‘Cool’ Mode: Evidence from the Cyclic Adriatic Platform, Croatia
Sedimentology (2007) 54, 317–337 doi: 10.1111/j.1365-3091.2006.00837.x The Late Jurassic Tithonian, a greenhouse phase in the Middle Jurassic–Early Cretaceous ‘cool’ mode: evidence from the cyclic Adriatic Platform, Croatia ANTUN HUSINEC* and J. FRED READ *Croatian Geological Survey, Sachsova 2, HR-10000 Zagreb, Croatia Department of Geosciences, Virginia Tech, 4044 Derring Hall, Blacksburg, VA 24061, USA (E-mail: [email protected]) ABSTRACT Well-exposed Mesozoic sections of the Bahama-like Adriatic Platform along the Dalmatian coast (southern Croatia) reveal the detailed stacking patterns of cyclic facies within the rapidly subsiding Late Jurassic (Tithonian) shallow platform-interior (over 750 m thick, ca 5–6 Myr duration). Facies within parasequences include dasyclad-oncoid mudstone-wackestone-floatstone and skeletal-peloid wackestone-packstone (shallow lagoon), intraclast-peloid packstone and grainstone (shoal), radial-ooid grainstone (hypersaline shallow subtidal/intertidal shoals and ponds), lime mudstone (restricted lagoon), fenestral carbonates and microbial laminites (tidal flat). Parasequences in the overall transgressive Lower Tithonian sections are 1– 4Æ5 m thick, and dominated by subtidal facies, some of which are capped by very shallow-water grainstone-packstone or restricted lime mudstone; laminated tidal caps become common only towards the interior of the platform. Parasequences in the regressive Upper Tithonian are dominated by peritidal facies with distinctive basal oolite units and well-developed laminate caps. Maximum water depths of facies within parasequences (estimated from stratigraphic distance of the facies to the base of the tidal flat units capping parasequences) were generally <4 m, and facies show strongly overlapping depth ranges suggesting facies mosaics. Parasequences were formed by precessional (20 kyr) orbital forcing and form parasequence sets of 100 and 400 kyr eccentricity bundles. -
Polychaeta, Annelida)
Carnets de Géologie / Notebooks on Geology - Letter CG2011/05 (CG2011_L05) Evolution of a dense outer protective tube layer in serpulids (Polychaeta, Annelida) 1 Olev VINN 2 Elena K. KUPRIYANOVA Abstract: Although the walls of most serpulid tubes are homogeneous, tubes of certain species may contain up to four ultrastructurally distinct layers. Some of these layers are made of densely packed large crystals and others are composed of sparsely packed fine crystals. In almost all (16 of 17) examined species having layered tubes, the dense layer is located in the outer wall part and the layer(s) composed of fine and relatively sparsely packed crystals are positioned in the inner wall part. Two species have transparent tube walls made entirely of densely packed crystals. Fossil serpulid tubes with dense outer layers (DOL) are known from the Late Cretaceous (Pentaditrupa subtorquata) and the Eocene (Pyrgopolon cf. mellevillei and Rotularia spirulaea). DOL gives a characteristic smooth shiny appearance to the tube surface and presumably evolved as an adaptation against drilling predation by gastropods and to delay shell dissolution in the waters of the deep-sea under-saturated with calcium carbonate. Key Words: Serpulidae; biomineralization; tube ultrastructure; evolution. Citation : VINN O. & KUPRIYANOVA E.K. (2011).- Evolution of a dense outer protective tube layer in serpulids (Polychaeta, Annelida).- Carnets de Géologie / Notebooks on Geology, Brest, Letter 2011/05 (CG2011_L05), p. 137-147. Résumé : Évolution de la couche externe, dense et protectrice, du tube de Serpulidés (Polychètes, Annélides).- Alors que les parois de la plupart des tubes de Serpulidés sont homogènes, les tubes de quelques espèces peuvent présenter jusqu'à quatre couches à ultrastructures variées. -
A Comparison of the Dinosaur Communities from the Middle
Preprints (www.preprints.org) | NOT PEER-REVIEWED | Posted: 31 July 2018 doi:10.20944/preprints201807.0610.v1 Peer-reviewed version available at Geosciences 2018, 8, 327; doi:10.3390/geosciences8090327 1 Review 2 A comparison of the dinosaur communities from 3 the Middle Jurassic of the Cleveland (Yorkshire) 4 and Hebrides (Skye) basins, based on their ichnites 5 6 Mike Romano 1*, Neil D. L. Clark 2 and Stephen L. Brusatte 3 7 1 Independent Researcher, 14 Green Lane, Dronfield, Sheffield S18 2LZ, England, United Kingdom; 8 [email protected] 9 2 Curator of Palaeontology, The Hunterian, University of Glasgow, University Avenue, Glasgow 10 G12 8QQ, Scotland, United Kingdom; [email protected] 11 3 Chancellor's Fellow in Vertebrate Palaeontology, School of Geosciences, University of Edinburgh, 12 Grant Institute, The King's Buildings, James Hutton Road, Edinburgh EH9 3FE, Scotland, United Kingdom; 13 [email protected] 14 * Correspondence: [email protected]; Tel.: 01246 417330 15 16 Abstract: 17 Despite the Hebrides and Cleveland basins being geographically close, research has not 18 previously been carried out to determine faunal similarities and assess the possibility of links 19 between the dinosaur populations. The palaeogeography of both areas during the Middle Jurassic 20 shows that there were no elevated landmasses being eroded to produce conglomeratic material in 21 the basins at that time. The low-lying landscape and connected shorelines may have provided 22 connectivity between the two dinosaur populations. 23 The dinosaur fauna of the Hebrides and Cleveland basins has been assessed based primarily 24 on the abundant ichnites found in both areas as well as their skeletal remains. -
The Marine Fauna of New Zealand : Spirorbinae (Polychaeta : Serpulidae)
ISSN 0083-7903, 68 (Print) ISSN 2538-1016; 68 (Online) The Marine Fauna of New Zealand : Spirorbinae (Polychaeta : Serpulidae) by PETER J. VINE ANOGlf -1,. �" ii 'i ,;.1, J . --=--� • ��b, S�• 1 • New Zealand Oceanographic Institute Memoir No. 68 1977 The Marine Fauna of New Zealand: Spirorbinae (Polychaeta: Serpulidae) This work is licensed under the Creative Commons Attribution-NonCommercial-NoDerivs 3.0 Unported License. To view a copy of this license, visit http://creativecommons.org/licenses/by-nc-nd/3.0/ Frontispiece Spirorbinae on a piece of alga washed up on the New Zealand seashore. This work is licensed under the Creative Commons Attribution-NonCommercial-NoDerivs 3.0 Unported License. To view a copy of this license, visit http://creativecommons.org/licenses/by-nc-nd/3.0/ NEW ZEALAND DEPARTMENT OF SCIENTIFIC AND INDUSTRIAL RESEARCH The Marine Fauna of New Zealand: Spirorbinae (Polychaeta: Serpulidae) by PETER J. VINE Department of Zoology, University College, Singleton Park, Swansea, Wales, UK and School of Biological Sciences, James Cook University of North Queensland, Townsville, Australia PERMANENT ADDRESS "Coe! na Mara", Faul, c/- Dr Casey, Clifden, County Galway, Ireland New Zealand Oceanographic Institute Memoir No. 68 1977 This work is licensed under the Creative Commons Attribution-NonCommercial-NoDerivs 3.0 Unported License. To view a copy of this license, visit http://creativecommons.org/licenses/by-nc-nd/3.0/ Citation according to World list of Scientific Periodicals (4th edition: Mem. N.Z. oceanogr. Inst. 68 ISSN 0083-7903 Received for publication at NZOI January 1973 Edited by T. K. Crosby, Science InformationDivision, DSIR and R. -
And Early Jurassic Sediments, and Patterns of the Triassic-Jurassic
and Early Jurassic sediments, and patterns of the Triassic-Jurassic PAUL E. OLSEN AND tetrapod transition HANS-DIETER SUES Introduction parent answer was that the supposed mass extinc- The Late Triassic-Early Jurassic boundary is fre- tions in the tetrapod record were largely an artifact quently cited as one of the thirteen or so episodes of incorrect or questionable biostratigraphic corre- of major extinctions that punctuate Phanerozoic his- lations. On reexamining the problem, we have come tory (Colbert 1958; Newell 1967; Hallam 1981; Raup to realize that the kinds of patterns revealed by look- and Sepkoski 1982, 1984). These times of apparent ing at the change in taxonomic composition through decimation stand out as one class of the great events time also profoundly depend on the taxonomic levels in the history of life. and the sampling intervals examined. We address Renewed interest in the pattern of mass ex- those problems in this chapter. We have now found tinctions through time has stimulated novel and com- that there does indeed appear to be some sort of prehensive attempts to relate these patterns to other extinction event, but it cannot be examined at the terrestrial and extraterrestrial phenomena (see usual coarse levels of resolution. It requires new fine- Chapter 24). The Triassic-Jurassic boundary takes scaled documentation of specific faunal and floral on special significance in this light. First, the faunal transitions. transitions have been cited as even greater in mag- Stratigraphic correlation of geographically dis- nitude than those of the Cretaceous or the Permian junct rocks and assemblages predetermines our per- (Colbert 1958; Hallam 1981; see also Chapter 24). -
Universidad Autónoma De Nuevo León Facultad De Ciencias De La Tierra
UNIVERSIDAD AUTÓNOMA DE NUEVO LEÓN FACULTAD DE CIENCIAS DE LA TIERRA "ANÁLISIS DE MICROFACIES Y PALEOICTIOLOGÍA DE LA FORMACIÓN AGUA NUEVA (CRETÁCICO SUPERIOR) EN LA SIERRA DE SAN CARLOS, TAMAULIPAS, MÉXICO" TESIS QUE COMO REQUISITO PARCIAL PARA OBTENER EL GRADO DE MAESTRO EN CIENCIAS GEOLÓGICAS PRESENTA: LAURA ALEJANDRA SANTANA SALAS LINARES, NUEVO LEÓN JUNIO 2012 UNIVERSIDAD AUTÓNOMA DE NUEVO LEÓN FACULTAD DE CIENCIAS DE LA TIERRA HDA. DE GUADALUPE, CARR. A CERRO PRIETO KM 8, A.P. 104 67700 LINARES, NUEVO LEÓN, MÉXICO TELS. Y FAX (821) 214 20 10, 214 20 20 Y 214 20 30 “ANÁLISIS DE MICROFACIES Y PALEOICTIOLOGÍA DE LA FORMACIÓN AGUA NUEVA (CRETÁCICO SUPERIOR) EN LA SIERRA DE SAN CARLOS, TAMAULIPAS, MÉXICO” PRESENTA: LAURA ALEJANDRA SANTANA SALAS HA SIDO ACEPTADA COMO REQUISITO PARCIAL PARA OBTENER EL GRADO DE: MAESTRO EN CIENCIAS GEOLÓGICAS Vo. Bo. DIRECTOR DE TESIS ___________________________________ Dr. José Guadalupe López Oliva LINARES, NUEVO LEÓN JUNIO 2012 UNIVERSIDAD AUTÓNOMA DE NUEVO LEÓN FACULTAD DE CIENCIAS DE LA TIERRA HDA. DE GUADALUPE, CARR. A CERRO PRIETO KM 8, A.P. 104 67700 LINARES, NUEVO LEÓN, MÉXICO TELS. Y FAX (821) 214 20 10, 214 20 20 Y 214 20 30 “ANÁLISIS DE MICROFACIES Y PALEOICTIOLOGÍA DE LA FORMACIÓN AGUA NUEVA (CRETÁCICO SUPERIOR) EN LA SIERRA DE SAN CARLOS, TAMAULIPAS, MÉXICO” PRESENTA: LAURA ALEJANDRA SANTANA SALAS HA SIDO ACEPTADA COMO REQUISITO PARCIAL PARA OBTENER EL GRADO DE: MAESTRO EN CIENCIAS GEOLÓGICAS COMITÉ DE REVISIÓN Vo. Bo. ___________________________________ Dr. José Guadalupe López Oliva Director de Tesis ____________________________ ________________________ Dr. Juan Alonso Ramírez Fernández M. C. Andres Ramos Ledezma Co-Director de Tesis Co-Director de Tesis ______________________________ Dra.