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Early Cretaceous (Albian) Decapods from the Glen Rose and Walnut Formations of Texas, USA
Bulletin of the Mizunami Fossil Museum, no. 42 (2016), p. 1–22, 11 fi gs., 3 tables. © 2016, Mizunami Fossil Museum Early Cretaceous (Albian) decapods from the Glen Rose and Walnut formations of Texas, USA Carrie E. Schweitzer*, Rodney M. Feldmann**, William L. Rader***, and Ovidiu Fran㶥escu**** *Department of Geology, Kent State University at Stark, 6000 Frank Ave. NW, North Canton, OH 44720 USA <[email protected]> **Department of Geology, Kent State University, Kent, OH 44242 USA ***8210 Bent Tree Road, #219, Austin, TX 78759 USA ****Division of Physical and Computational Sciences, University of Pittsburgh Bradford, Bradford, PA 16701 USA Abstract Early Cretaceous (Albian) decapod crustaceans from the Glen Rose Limestone and the Walnut Formation include the new taxa Palaeodromites xestos new species, Rosadromites texensis new genus, new species, Karyosia apicava new genus new species, Aetocarcinus new genus, Aetocarcinus muricatus new species, and the new combinations Aetocarcinus roddai (Bishop, 1983), Necrocarcinus pawpawensis (Rathbun, 1935) and Necrocarcinus hodgesi (Bishop, 1983). These two formations have yielded a much less diverse decapod fauna than the nearly coeval and proximally deposited Pawpaw Formation. Paleoenvironment is suggested as a controlling factor in the decapod diversity of these units. Key words: Brachyura, Nephropidae, Dromiacea, Raninoida, Etyioidea, North America Introduction deposited in the shallow waters of a broad carbonate platform. Deposition occurred on the southeastern flank of Late Early Cretaceous decapod faunas from the Gulf the Llano Uplift and, on the seaward margin to the Coastal Plain of North America have been well reported northwest, behind the Stuart City Reef Trend. Coral and and described since the early part of the twentieth century rudist reefs, algal beds, extensive ripple marks, evaporites, (Rathbun, 1935; Stenzel, 1945). -
Papers in Press
Papers in Press “Papers in Press” includes peer-reviewed, accepted manuscripts of research articles, reviews, and short notes to be published in Paleontological Research. They have not yet been copy edited and/or formatted in the publication style of Paleontological Research. As soon as they are printed, they will be removed from this website. Please note they can be cited using the year of online publication and the DOI, as follows: Humblet, M. and Iryu, Y. 2014: Pleistocene coral assemblages on Irabu-jima, South Ryukyu Islands, Japan. Paleontological Research, doi: 10.2517/2014PR020. doi:10.2517/2018PR013 Features and paleoecological significance of the shark fauna from the Upper Cretaceous Hinoshima Formation, Himenoura Group, Southwest Japan Accepted Naoshi Kitamura 4-8-7 Motoyama, Chuo-ku Kumamoto, Kumamoto 860-0821, Japan (e-mail: [email protected]) Abstract. The shark fauna of the Upper Cretaceous Hinoshima Formation (Santonian: 86.3–83.6 Ma) of the manuscriptHimenoura Group (Kamiamakusa, Kumamoto Prefecture, Kyushu, Japan) was investigated based on fossil shark teeth found at five localities: Himedo Park, Kugushima, Wadanohana, Higashiura, and Kotorigoe. A detailed geological survey and taxonomic analysis was undertaken, and the habitat, depositional environment, and associated mollusks of each locality were considered in the context of previous studies. Twenty-one species, 15 genera, 11 families, and 6 orders of fossil sharks are recognized from the localities. This assemblage is more diverse than has previously been reported for Japan, and Lamniformes and Hexanchiformes were abundant. Three categories of shark fauna are recognized: a coastal region (Himedo Park; probably a breeding site), the coast to the open sea (Kugushima and Wadanohana), and bottom-dwelling or near-seafloor fauna (Kugushima, Wadanohana, Higashiura, and Kotorigoe). -
A New Assemblage of Plant Mesofossils (Late Turonian– Middle Santonian; Upper Cretaceous) from the Tamagawa Formation, Kuji Group, in Northeastern Japan
120Paleontological Research, vol. 25, no. 2, pp. 120–126, MasamichiApril 1, 2021 Takahashi et al. © by the Palaeontological Society of Japan doi:10.2517/2020PR015 A new assemblage of plant mesofossils (late Turonian– middle Santonian; Upper Cretaceous) from the Tamagawa Formation, Kuji Group, in northeastern Japan MASAMICHI TAKAHASHI1, PATRICK S. HERENDEEN2, FABIANY HERRERA2, REN HIRAYAMA3, HISAO ANDO4, KAZUHISA SASAKI5 and PETER R. CRANE6,7 1Department of Environmental Sciences, Niigata University, 8050, 2-cho, Ikarashi, Nishi-ku, Niigata 950-2181, Japan (e-mail: [email protected]) 2Chicago Botanic Garden, 1000 Lake Cook Road, Glencoe, Illinois 60022, USA 3School of International Liberal Studies, Waseda University, 1-7-14, Nishiwaseda, Shinjuku-ku, Tokyo 169-0051, Japan 4Department of Earth Sciences, Faculty of Science, Ibaraki University, 2-1-1, Bunkyo, Mito 310-8512, Japan 5Kuji Amber Museum, 19-156-133, Kokujicho, Kuji, Iwate 028-0071, Japan 6Yale School of the Environment, Yale University, 195, Prospect Street, New Haven, Connecticut 06511, USA 7Oak Spring Garden Foundation, 1776, Loughborough Lane, Upperville, Virginia 20184, USA Received November 14, 2019; Revised manuscript accepted March 4, 2020 Abstract. A preliminary description is provided of a new assemblage of small, three-dimensional and char- coalified mesofossils from the Tamagawa Formation (late Turonian–middle Santonian; Upper Cretaceous) of the Kuji Group in northeastern Japan. The new mesofossils yield excellent structural details and include well- preserved circinate shoots of ferns together with conifer leafy-shoots, seeds and probable pollen cones, and vari- ety of angiosperm fruits and seeds, including fruits of Cornales and seeds of Nymphaeales. The new mesofossil assemblage is complementary to the previously published macrofossil flora from the Kuji Group. -
Botany (Effective from 2018 Admissions)
C. M. S. COLLEGE KOTTAYAM KERALA SYLLABUS FOR UNDERGRADUATE PROGRAMME IN BOTANY (EFFECTIVE FROM 2018 ADMISSIONS) RECOMMENDED BY: BOARD OF STUDIES, BOTANY C. M. S. COLLEGE, KOTTAYAM B Sc BotanySyllabus 2018 Admissiononwards B. Sc. BOTANY PROGRAMME PROGRAMME DESIGN The UG programme in Botany must include (a) Common Courses*, (b) Core Courses (c) Complementary Courses (d) Open Course (e) Choice based Course and (f) Projectwork. No course shall carry more than 5 credits. The student shall select one Open course in Semester V offered by different departments in the same institution. The number of courses for the programme should contain 12 compulsory core courses,1 open course,1 elective course from the frontier area of the core courses, 6 core practical courses, 1project work, 8 complementary courses and 2 complementary practical courses. There should be 10 common courses,or otherwise specified, which includes the first and second language of study. PROGRAMME STRUCTURE: SUMMARY OF COURSES AND CREDITS No.of Total Sl. No. Coursetype courses credits 1 Common course I-English 6 22 2 Common course II– Additionallanguage 4 16 3 Core + Practical 12 + 6 46 4 ComplementaryI+ Practical 4 + 2 14 5 ComplementaryII+ Practical 4 + 2 14 6 Opencourse 1 3 7 Programme elective 1 3 8 Project work 1 2 Total 43 120 Totalcredits 120 Programme duration 6 Semesters Minimum attendance required 75% *Course: a segment of subject matter to be covered in a semester. Each course is designed variously under lectures /tutorials /laboratory or fieldwork /seminar /project /practical training /assignments /evalution etc., to meet effective teaching and learning needs. -
Titanosauriform Teeth from the Cretaceous of Japan
“main” — 2011/2/10 — 15:59 — page 247 — #1 Anais da Academia Brasileira de Ciências (2011) 83(1): 247-265 (Annals of the Brazilian Academy of Sciences) Printed version ISSN 0001-3765 / Online version ISSN 1678-2690 www.scielo.br/aabc Titanosauriform teeth from the Cretaceous of Japan HARUO SAEGUSA1 and YUKIMITSU TOMIDA2 1Museum of Nature and Human Activities, Hyogo, Yayoigaoka 6, Sanda, 669-1546, Japan 2National Museum of Nature and Science, 3-23-1 Hyakunin-cho, Shinjuku-ku, Tokyo 169-0073, Japan Manuscript received on October 25, 2010; accepted for publication on January 7, 2011 ABSTRACT Sauropod teeth from six localities in Japan were reexamined. Basal titanosauriforms were present in Japan during the Early Cretaceous before Aptian, and there is the possibility that the Brachiosauridae may have been included. Basal titanosauriforms with peg-like teeth were present during the “mid” Cretaceous, while the Titanosauria with peg-like teeth was present during the middle of Late Cretaceous. Recent excavations of Cretaceous sauropods in Asia showed that multiple lineages of sauropods lived throughout the Cretaceous in Asia. Japanese fossil records of sauropods are conformable with this hypothesis. Key words: Sauropod, Titanosauriforms, tooth, Cretaceous, Japan. INTRODUCTION humerus from the Upper Cretaceous Miyako Group at Moshi, Iwaizumi Town, Iwate Pref. (Hasegawa et al. Although more than twenty four dinosaur fossil local- 1991), all other localities provided fossil teeth (Tomida ities have been known in Japan (Azuma and Tomida et al. 2001, Tomida and Tsumura 2006, Saegusa et al. 1998, Kobayashi et al. 2006, Saegusa et al. 2008, Ohara 2008, Azuma and Shibata 2010). -
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. -
Life and Time of Indian Williamsonia
Life and time of Indian Williamsonia )ayasri Banerji Banerji, J 1992. Life and time of Indian Williamsonia. Palaeobotanist 40 : 245-259. The Williamsonia plant, belonging to the order Bennettitales, consists of stem-Bucklandia Presl, leaf Ptilophyllum Morris, male flower- Weltrichia Braun and female flower- Williamsonia Carruthers. This plant was perhaps a small, much branched woody tree of xerophytic environment. It co-existed alongwith extremely variable and rich flora including highly diversified plant groups from algae to gymnosperms. In India, it appeared during the marine Jurassic, proliferated and widely distributed in the Lower Cretaceous and disappeared from the vegetational scenario of Upper Cretaceous Period with the advent of angiosperms. Key-words-Bennettitales, Williamsonia, Jurassic-Cretaceous (India). jayasri Baner}i, Birbal Sahni Institute of Palaeobotany, 53 University Road, Lucknow 226007, India. ri~T ~ 'lfmftq- fili'<1QQ«lf.:lQi "" om~~ "l?li'O'$i'OI<1fl \f>'f it ~ filf<1QQ«lf.:lQi qtfr if ~ ~ 3!<'flT-3!<'flT 'lTIif it ~ "lTif t W'I'T CAT-~ m, ~ ~ ~it ~fu;m;;mrr~1 ~qtm~~ <ffir ll~<'ilf4>~<'1'i"li'tfGr, "''!'''l ~~?l~Ti:t>Qi <ilf.1 'I"lT filf<1QQ«lf.:lQi ~ ~ ~ f;;ru-if.~ ~ 61'1'~dOl'h\'i if m <'IT<'1T ~ Wc:r, 3!fuq,iffiliOlT3if it ~ ¥i "IT' ~ it il'1f4ff1"1ld, it if qtfr ~ 'it, q;r tt ~ ~tl W'I'T~~'-I'<"1if~~3lT, 3Tahmm'-l'<"1if~~~-~'d"f~<f"lT'3'1f'<mm~ ~ ~ ~ ~ if qtm if if t1T"f -flT"f lIT lfllT' LIFE OF WILLIAMSONIA PLANT B. dichotoma Sharma. In B. indica Seward, the secondary wood is more compact than recent cycads In the Upper Mesozoic Era, a new group of and cycadeoids. -
JUDD W.S. Et. Al. (2002) Plant Systematics: a Phylogenetic Approach. Chapter 7. an Overview of Green
UNCORRECTED PAGE PROOFS An Overview of Green Plant Phylogeny he word plant is commonly used to refer to any auto- trophic eukaryotic organism capable of converting light energy into chemical energy via the process of photosynthe- sis. More specifically, these organisms produce carbohydrates from carbon dioxide and water in the presence of chlorophyll inside of organelles called chloroplasts. Sometimes the term plant is extended to include autotrophic prokaryotic forms, especially the (eu)bacterial lineage known as the cyanobacteria (or blue- green algae). Many traditional botany textbooks even include the fungi, which differ dramatically in being heterotrophic eukaryotic organisms that enzymatically break down living or dead organic material and then absorb the simpler products. Fungi appear to be more closely related to animals, another lineage of heterotrophs characterized by eating other organisms and digesting them inter- nally. In this chapter we first briefly discuss the origin and evolution of several separately evolved plant lineages, both to acquaint you with these important branches of the tree of life and to help put the green plant lineage in broad phylogenetic perspective. We then focus attention on the evolution of green plants, emphasizing sev- eral critical transitions. Specifically, we concentrate on the origins of land plants (embryophytes), of vascular plants (tracheophytes), of 1 UNCORRECTED PAGE PROOFS 2 CHAPTER SEVEN seed plants (spermatophytes), and of flowering plants dons.” In some cases it is possible to abandon such (angiosperms). names entirely, but in others it is tempting to retain Although knowledge of fossil plants is critical to a them, either as common names for certain forms of orga- deep understanding of each of these shifts and some key nization (e.g., the “bryophytic” life cycle), or to refer to a fossils are mentioned, much of our discussion focuses on clade (e.g., applying “gymnosperms” to a hypothesized extant groups. -
Geologica Acta, Vol.4, N°4, 2006, 409-438 |415| Ce
'geológica FOmS^Y ACTA GEOLÓGICA HISPAfilCA Geológica acta: an international earth science journal Universidad de Barcelona [email protected] ISSN (Versión impresa): 1695-6133 ESPAÑA 2006 C.C. Labandeira THE FOUR PHASES OF PLANT-ARTHROPOD ASSOCIATIONS IN DEEP TIME Geológica acta: an international earth science journal, december, año/vol. 4, número 004 Universidad de Barcelona Barcelona, España pp. 409-438 Red de Revistas Científicas de América Latina y el Caribe, España y Portugal ®re¿!alyc^ Universidad Autónoma del Estado de México http://redalyc.uaemex.mx Geológica Acta, Vol.4, N° 4, 2006, 409-438 Appendix l-IX geología acta Available online at www.geologica-acta.com The Four Phases of Plant-Arthropod Associations in Deep Time C.C. LABANDEIRA |1||2| 111 Smithsonian Institution, National Museum of Natural History P.O. Box 37012, MRC-121 Department of Paleobiology, Washington, D.C., USA 200137012. E-mail: [email protected] 121 University of Maryland, Department of Entomology College Park, Maryland, USA 20742 1 ABSTRACT I Vascular-plant hosts, their arthropod herbivores, and associated functional feeding groups are distributed spa- tiotemporally into four major herbivore expansions during the past 420 m.y. They are: (1) a Late Silurian to Late Devonian (60 m.y.) phase of myriapod and apterygote, hexapod (perhaps pterygote) herbivores on several clades of primitive vascular-plant hosts and a prototaxalean fungus; (2) a Late Mississippian to end-Permian (85 m.y.) phase of mites and apterygote and basal pterygote herbivores on pteridophyte and basal gymnospermous plant hosts; (3) a Middle Triassic to Recent (245 m.y.) phase of mites, orthopteroids (in the broadest sense) and hemipteroid and basal holometabolan herbivores on pteridophyte and gymnospermous plant hosts; and (4) a mid Early Cretaceous to Recent (115 m.y.) phase of modern-aspect orthopteroids and derived hemipteroid and holometabolous herbivores on angiospermous plant hosts. -
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). -
Reconstructions of the Continents Around the North Atlantic at About the 60Th Parallel
CORE Metadata, citation and similar papers at core.ac.uk Provided by RERO DOC Digital Library 1 Published in Earth and Planetary Science Letters 187: 55-69, 2001 Reconstructions of the continents around the North Atlantic at about the 60th parallel Trond H. Torsvik a;d, Rob Van der Voo b;*, Joseph G. Meert a;e, Jon Mosar a, Harald J. Walderhaug c a VISTA, c/o Geological Survey of Norway, Leiv Eiriksonsvei 39, N-7491 Trondheim, Norway b Department of Geological Sciences, University of Michigan, Ann Arbor, MI 48109-1063, USA c University of Bergen, Institute of Solid Earth Physics, Allegt. 41, N-5007Bergen, Norway d Institute for Petroleum Technology and Applied Geophysics, S.P. Andersens v. 15a, N-7491 Trondheim, NTNU, Norway e Department of Geography and Geology, Indiana State University, Terre Haute, IN 47809, USA Received 12 September 2000; received in revised form 16 February 2001; accepted 21 February 2001 Abstract Late Carboniferous^Early Tertiary apparent polar wander (APW) paths (300^40 Ma) for North America and Europe have been tested in various reconstructions. These paths demonstrate that the 500 fathom Bullard et al. fit is excellent from Late Carboniferous to Late Triassic times, but the continental configuration in northern Pangea changed systematically between the Late Triassic (ca. 214 Ma) and the Mid-Jurassic (ca. 170 Ma) due to pre-drift extension. Best fit North Atlantic reconstructions minimize differences in the Late Carboniferous^Early Jurassic and Late Cretaceous^ Tertiary segments of the APW paths, but an enigmatic difference exists in the paths for most of the Jurassic, whereas for the Early Cretaceous the data from Europe are nearly non-existent. -
Deep Sea Drilling Project Initial Reports Volume 6
39. PLANKTONIC MICROFOSSIL BIOSTRATIGRAPHY OF THE NORTHWESTERN PACIFIC OCEAN David Bukry1, U.S. Geological Survey, La Jolla, California, Robert G. Douglas, Case Western Reserve University, Cleveland, Ohio, Stanley A. Kling, Cities Service Oil Company, Tulsa, Oklahoma, and Valeri Krasheninnikov, Academy of Sciences of the U.S.S.R., Moscow CONTENTS Page Page Introduction 1253 Regional Correlation 1281 Zonal Comparison 1254 Calcareous Nannoplankton 1281 Planktonic Foraminifera, Mesozoic 1281 Upper Cretaceous-Paleocene Boundary 1255 California 1281 Paleocene-Eocene Boundary 1259 Japan 1285 Eocene-Oligocene Boundary 1259 West Pacific 1286 Oligocene-Miocene Boundary 1259 Australia 1287 Miocene-Pliocene Boundary 1260 Planktonic Foraminifera, Cenozoic 1288 Pliocene-Pleistocene Boundary 1261 Solomon Islands 1288 Zonal Summary 1261 Mariana Islands 1288 The Philippines 1288 Paleoecology 1261 Taiwan 1289 Calcareous Nannoplankton 1261 Japan 1289 Radiolaria 1267 Kamchatka Penisula 1290 California 1290 Preservation 1267 Radiolaria 1291 Calcareous Nannoplankton 1267 Sedimentation Rates 1291 Foraminifera 1269 Relationship to Acoustostratigraphy 1294 Radiolaria 1279 References 1296 INTRODUCTION A comparison of zonal units of calcareous nannoplank- ton, foraminifera, and radiolarians in the same strata Biostratigraphic evidence obtained from the north- shows only few cases of exact coincidence of zonal western Pacific Ocean as a result of coring carried out limits, especially if coincidences at the top or bottom by the Glomar Challenger during Leg 6 of the Deep of the standard 9-meter coring runs are dismissed as Sea Drilling Project from Hawaii to Guam is considered artificially induced owing to gaps in sediment recovery. here mainly from the standpoint of three dominant Exact coincidence of zonal limits within coring runs marine planktonic microfossil groups—calcareous nan- are most notable for the Upper Paleocene sediment of noplankton, foraminifers, and radiolarians.