The Cenozoic Era - Nýlífsöld 65 MY-Present Jarðsaga 2 Ólafur Ingólfsson Origin of the Term: the Tertiary Tertiary System
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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. -
Crustacea: Thalassinidea, Brachyura) from Puerto Rico, United States Territory
Bulletin of the Mizunami Fossil Museum, no. 34 (2008), p. 1–15, 6 figs., 1 table. © 2008, Mizunami Fossil Museum New Cretaceous and Cenozoic Decapoda (Crustacea: Thalassinidea, Brachyura) from Puerto Rico, United States Territory Carrie E. Schweitzer1, Jorge Velez-Juarbe2, Michael Martinez3, Angela Collmar Hull1, 4, Rodney M. Feldmann4, and Hernan Santos2 1)Department of Geology, Kent State University Stark Campus, 6000 Frank Ave. NW, North Canton, Ohio, 44720, USA <[email protected]> 2)Department of Geology, University of Puerto Rico, Mayagüez Campus, P. O. Box 9017, Mayagüez, Puerto Rico, 00681 United States Territory <[email protected]> 3)College of Marine Science, University of South Florida, 140 7th Ave. South, St. Petersburg, Florida 33701, USA <[email protected]> 4)Department of Geology, Kent State University, Kent, Ohio 44242, USA <[email protected]> Abstract A large number of recently collected specimens from Puerto Rico has yielded two new species including Palaeoxanthopsis tylotus and Eurytium granulosum, the oldest known occurrence of the latter genus. Cretaceous decapods are reported from Puerto Rico for the first time, and the Cretaceous fauna is similar to that of southern Mexico. Herein is included the first report of Pleistocene decapods from Puerto Rico, which were previously known from other Caribbean localities. The Pleistocene Cardisoma guanhumi is a freshwater crab of the family Gecarcinidae. The freshwater crab families have a poor fossil record; thus, the occurrence is noteworthy and may document dispersal of the crab by humans. Key words: Decapoda, Thalassinidea, Brachyura, Puerto Rico, Cretaceous, Paleogene, Neogene. Introduction than Eocene are not separated by these fault zones and even overlie parts of the fault zones in some areas (Jolly et al., 1998). -
New Paleocene Skeletons and the Relationship of Plesiadapiforms to Crown-Clade Primates
New Paleocene skeletons and the relationship of plesiadapiforms to crown-clade primates Jonathan I. Bloch*†, Mary T. Silcox‡, Doug M. Boyer§, and Eric J. Sargis¶ʈ *Florida Museum of Natural History, University of Florida, P. O. Box 117800, Gainesville, FL 32611; ‡Department of Anthropology, University of Winnipeg, 515 Portage Avenue, Winnipeg, MB, Canada, R3B 2E9; §Department of Anatomical Science, Stony Brook University, Stony Brook, NY 11794-8081; ¶Department of Anthropology, Yale University, P. O. Box 208277, New Haven, CT 06520; and ʈDivision of Vertebrate Zoology, Peabody Museum of Natural History, Yale University, New Haven, CT 06520 Communicated by Alan Walker, Pennsylvania State University, University Park, PA, November 30, 2006 (received for review December 6, 2005) Plesiadapiforms are central to studies of the origin and evolution preserved cranium of a paromomyid (10) seemed to independently of primates and other euarchontan mammals (tree shrews and support a plesiadapiform–dermopteran link, leading to the wide- flying lemurs). We report results from a comprehensive cladistic spread acceptance of this phylogenetic hypothesis. The evidence analysis using cranial, postcranial, and dental evidence including supporting this interpretation has been questioned (7, 9, 13, 15, 16, data from recently discovered Paleocene plesiadapiform skeletons 19, 20), but no previous study has evaluated the plesiadapiform– (Ignacius clarkforkensis sp. nov.; Dryomomys szalayi, gen. et sp. dermopteran link by using cranial, postcranial, and dental evidence, -
8. Primate Evolution
8. Primate Evolution Jonathan M. G. Perry, Ph.D., The Johns Hopkins University School of Medicine Stephanie L. Canington, B.A., The Johns Hopkins University School of Medicine Learning Objectives • Understand the major trends in primate evolution from the origin of primates to the origin of our own species • Learn about primate adaptations and how they characterize major primate groups • Discuss the kinds of evidence that anthropologists use to find out how extinct primates are related to each other and to living primates • Recognize how the changing geography and climate of Earth have influenced where and when primates have thrived or gone extinct The first fifty million years of primate evolution was a series of adaptive radiations leading to the diversification of the earliest lemurs, monkeys, and apes. The primate story begins in the canopy and understory of conifer-dominated forests, with our small, furtive ancestors subsisting at night, beneath the notice of day-active dinosaurs. From the archaic plesiadapiforms (archaic primates) to the earliest groups of true primates (euprimates), the origin of our own order is characterized by the struggle for new food sources and microhabitats in the arboreal setting. Climate change forced major extinctions as the northern continents became increasingly dry, cold, and seasonal and as tropical rainforests gave way to deciduous forests, woodlands, and eventually grasslands. Lemurs, lorises, and tarsiers—once diverse groups containing many species—became rare, except for lemurs in Madagascar where there were no anthropoid competitors and perhaps few predators. Meanwhile, anthropoids (monkeys and apes) emerged in the Old World, then dispersed across parts of the northern hemisphere, Africa, and ultimately South America. -
GEOLOGIC TIME SCALE V
GSA GEOLOGIC TIME SCALE v. 4.0 CENOZOIC MESOZOIC PALEOZOIC PRECAMBRIAN MAGNETIC MAGNETIC BDY. AGE POLARITY PICKS AGE POLARITY PICKS AGE PICKS AGE . N PERIOD EPOCH AGE PERIOD EPOCH AGE PERIOD EPOCH AGE EON ERA PERIOD AGES (Ma) (Ma) (Ma) (Ma) (Ma) (Ma) (Ma) HIST HIST. ANOM. (Ma) ANOM. CHRON. CHRO HOLOCENE 1 C1 QUATER- 0.01 30 C30 66.0 541 CALABRIAN NARY PLEISTOCENE* 1.8 31 C31 MAASTRICHTIAN 252 2 C2 GELASIAN 70 CHANGHSINGIAN EDIACARAN 2.6 Lopin- 254 32 C32 72.1 635 2A C2A PIACENZIAN WUCHIAPINGIAN PLIOCENE 3.6 gian 33 260 260 3 ZANCLEAN CAPITANIAN NEOPRO- 5 C3 CAMPANIAN Guada- 265 750 CRYOGENIAN 5.3 80 C33 WORDIAN TEROZOIC 3A MESSINIAN LATE lupian 269 C3A 83.6 ROADIAN 272 850 7.2 SANTONIAN 4 KUNGURIAN C4 86.3 279 TONIAN CONIACIAN 280 4A Cisura- C4A TORTONIAN 90 89.8 1000 1000 PERMIAN ARTINSKIAN 10 5 TURONIAN lian C5 93.9 290 SAKMARIAN STENIAN 11.6 CENOMANIAN 296 SERRAVALLIAN 34 C34 ASSELIAN 299 5A 100 100 300 GZHELIAN 1200 C5A 13.8 LATE 304 KASIMOVIAN 307 1250 MESOPRO- 15 LANGHIAN ECTASIAN 5B C5B ALBIAN MIDDLE MOSCOVIAN 16.0 TEROZOIC 5C C5C 110 VANIAN 315 PENNSYL- 1400 EARLY 5D C5D MIOCENE 113 320 BASHKIRIAN 323 5E C5E NEOGENE BURDIGALIAN SERPUKHOVIAN 1500 CALYMMIAN 6 C6 APTIAN LATE 20 120 331 6A C6A 20.4 EARLY 1600 M0r 126 6B C6B AQUITANIAN M1 340 MIDDLE VISEAN MISSIS- M3 BARREMIAN SIPPIAN STATHERIAN C6C 23.0 6C 130 M5 CRETACEOUS 131 347 1750 HAUTERIVIAN 7 C7 CARBONIFEROUS EARLY TOURNAISIAN 1800 M10 134 25 7A C7A 359 8 C8 CHATTIAN VALANGINIAN M12 360 140 M14 139 FAMENNIAN OROSIRIAN 9 C9 M16 28.1 M18 BERRIASIAN 2000 PROTEROZOIC 10 C10 LATE -
An Anachronistic Clarkforkian Mammal Fauna from the Paleocene Fort Union Formation (Great Divide Basin, Wyoming, USA)
Geologica Acta, Vol.7, Nos 1-2, March-June 2009, 113-124 DOI: 10.1344/105.000000274 Available online at www.geologica-acta.com An anachronistic Clarkforkian mammal fauna from the Paleocene Fort Union Formation (Great Divide Basin, Wyoming, USA) 1 2 ROBERT L. ANEMONE and WENDY DIRKS 1 Department of Anthropology. Western Michigan University Kalamazoo, MI 49008-5306, USA. E-mail: [email protected] 2 Oral Biology, School of Dental Sciences. Newcastle University Framlington Place. Newcastle-upon-Tyne, NE2 4BW, United Kingdom. E-mail: [email protected] ABSTRACT The Clarkforkian (latest Paleocene) North American Land Mammal Age (NALMA) remains a relatively poorly sampled biostratigraphic interval at the close of the Paleocene epoch that is best known from the Bighorn Basin of northwestern Wyoming. A period of global warming between the cooler early and middle Paleocene and the extreme warming of the early Eocene, the Clarkforkian witnessed significant floral and faunal turnover with important ramifications for the development of Cenozoic biotas. The combination of warming global climates with mammalian turnover (including likely intercontinental dispersals) marks the Clarkforkian and the succeeding Wasatchian (Earliest Eocene) NALMAs as periods of intense interest to paleobiologists and other earth scientists concerned with aspects of biostratigraphy and with the biotic effects of climate change in the past. In this paper we describe a new Clarkforkian mammalian fauna from the Great Divide Basin of southwestern Wyoming with some surprising faunal elements that differ from the typical suite of taxic associations found in Clarkforkian assemblages of the Bighorn Basin. Several different scenarios are explored to explain this “anachronistic” assem- blage of mammals from southern Wyoming in relation to the typical patterns found in northern Wyoming, includ- ing the concepts of basin-margin faunas, latitudinal and climatic gradients, and a chronologically transitional fau- na. -
Body Size, Extinction Events, and the Early Cenozoic Record of Veneroid Bivalves: a New Role for Recoveries?
Paleobiology, 31(4), 2005, pp. 578±590 Body size, extinction events, and the early Cenozoic record of veneroid bivalves: a new role for recoveries? Rowan Lockwood Abstract.ÐMass extinctions can play a role in shaping macroevolutionary trends through time, but the contribution of recoveries to this process has yet to be examined in detail. This study focuses on the effects of three extinction events, the end-Cretaceous (K/T), mid-Eocene (mid-E), and end- Eocene (E/O), on long-term patterns of body size in veneroid bivalves. Systematic data were col- lected for 719 species and 140 subgenera of veneroids from the Late Cretaceous through Oligocene of North America and Europe. Centroid size measures were calculated for 101 subgenera and glob- al stratigraphic ranges were used to assess extinction selectivity and preferential recovery. Vene- roids underwent a substantial extinction at the K/T boundary, although diversity recovered to pre- extinction levels by the early Eocene. The mid-E and E/O events were considerably smaller and their recovery intervals much shorter. None of these events were characterized by signi®cant ex- tinction selectivity according to body size at the subgenus level; however, all three recoveries were strongly size biased. The K/T recovery was biased toward smaller veneroids, whereas both the mid-E and E/O recoveries were biased toward larger ones. The decrease in veneroid size across the K/T recovery actually reinforced a Late Cretaceous trend toward smaller sizes, whereas the increase in size resulting from the Eocene recoveries was relatively short-lived. Early Cenozoic changes in predation, temperature, and/or productivity may explain these shifts. -
Foraging Behaviour of the Slender Loris (Loris Lydekkerianus Lydekkerianus): Implications for Theories of Primate Origins
Journal of Human Evolution 49 (2005) 289e300 Foraging behaviour of the slender loris (Loris lydekkerianus lydekkerianus): implications for theories of primate origins K.A.I. Nekaris* Department of Anthropology, Washington University, Campus Box 1114, One Brookings Drive, St. Louis, MO 63110, USA Received 3 May 2004; accepted 18 April 2005 Abstract Members of the Order Primates are characterised by a wide overlap of visual fields or optic convergence. It has been proposed that exploitation of either insects or angiosperm products in the terminal branches of trees, and the corresponding complex, three-dimensional environment associated with these foraging strategies, account for visual convergence. Although slender lorises (Loris sp.) are the most visually convergent of all the primates, very little is known about their feeding ecology. This study, carried out over 10 ½ months in South India, examines the feeding behaviour of L. lydekkerianus lydekkerianus in relation to hypotheses regarding visual predation of insects. Of 1238 feeding observations, 96% were of animal prey. Lorises showed an equal and overwhelming preference for terminal and middle branch feeding, using the undergrowth and trunk rarely. The type of prey caught on terminal branches (Lepidoptera, Odonata, Homoptera) differed significantly from those caught on middle branches (Hymenoptera, Coleoptera). A two-handed catch accompanied by bipedal postures was used almost exclusively on terminal branches where mobile prey was caught, whereas the more common capture technique of one-handed grab was used more often on sturdy middle branches to obtain slow moving prey. Although prey was detected with senses other than vision, vision was the key sense used upon the final strike. -
Geologic Time 8Th Grade .Pptx
3/24/15 Geologic Geologic Time Scale Time Scale • Division of Eon Earth’s history The longest of all based on the subdivision based types of life on the abundance forms that lived of certain fossils only during certain periods. Eras Era | Period • 2nd longest subdivision • Marked by worldwide changes in types of fossils. Periods • Units of geologic Ime marked by the types of life exisIng worldwide at the Ime. Trilobites are seen in many epochs different geological periods - Smallest of geologic divisions as different species. - Characterized by different life forms. - Some differences vary from conInent to content. Different species in different Ime period can be used as index fossils. 1 3/24/15 FOUR Eras… Precambrian Era • The earliest and longest geologic era • PRE-CAMBRIAN – 88% of earth’s history lasIng about 4.5 billion years. • LiXle is known of organisms of this era. • Paleozoic (ancient life) *due to rock having been destroyed. – 544 million years ago…lasted 300 million yrs • Mesozoic (middle life) – 245 million years ago…lasted 180 million yrs • Cenozoic (recent life) – 65 million years ago…conInues through present day Ediacarans Cyanobacteria in the Precambrian Era Ancient jellyfish like creature appeared are the earliest life forms known to man. near the end of the Precambrian Ear. The Appalachian Mountain were formed The Paleozoic Era in the Paleozoic era. • Large shallow seas covered much of the conInents. • Many of the fossils found have been marine (ocean) creatures and plants. 2 3/24/15 The Devonian Period Carboniferous Period 419-359 million years ago 359 – 299 million years ago (age of the fishes) Saw the emergence of early Saw the development of early sharks. -
Volume 26C-Nogrid
Priscum Volume 26 | Issue 1 May 2021 The Newsletter of the Paleontological Society Inside this issue Diversity, Equity, and Inclusion Matter in Diversity, Equity, & Inclusion matter in Paleontology Paleontology PS Development Developments Building an inclusive and equitable Where are we now? PaleoConnect Paleontological Society (see Section 12 of the Member Code of Conduct for definitions) is Since the Paleontological Society (PS) was Journal Corner essential to realizing our core purpose — founded in 1908, its membership has been advancing the field of paleontology (see Article dominated by white men from the United PS-AGI Summer 2020 Interns II of the Articles of Incorporation). However, like States. Racial and ethnic diversity in the PS many other scientific societies, ours has remain extremely low. More than 88% of Tribute to William Clemens, Jr. historically only fostered a sense of belonging respondents to PS membership surveys Educational Materials for a subset of individuals. conducted in 2013 and 2019 self-identified as White (Stigall, 2013; unpublished data, 2019). PS Ethics Committee Report Consider your outreach experiences. Imagine These surveys revealed that, unlike the visiting a series of first grade classrooms — proportion of women, which has increased in Research and Grant Awardees overwhelmingly, the children are fascinated by younger age cohorts (Stigall, 2013), racial and PS Annual meeting at GSA Connects dinosaur bones, scale trees, and trilobites — ethnic diversity varied little among age groups, 2021 regardless of their identities. Now, reflect on suggesting that substantial barriers to the your experiences in paleontological settings as inclusion of most racial and ethnic groups have Upcoming Opportunities an adult; do they include as much diversity as persisted across generations of PS members. -
Paleontology 9: Cenozoic
PALEONTOLOGY 9: CENOZOIC VOLUME 9, ISSUE 9, SEPTEMBER 2020 AGE OF MAMMALS THIS MONTH This issue on the Cenozoic Era • Cenozoic Dioramas page 2 is the last in the Paleontology series. The Cenozoic Era • Complete Your Timeline! page 9 covers the time from the end of dinosaurs to present day. • DNA Mutations • Build Models page 19 Over the course of this series, • Bit of Wobble page 26 we have included information • Meiosis page 33 and activities on DNA. DNA, the • Lethal Gene page 35 blueprint for all life, is the • Mutations page 43 foundation of biology. A fundamental understanding of Megatherium americanum is the POWER WORDS DNA helps us to understand largest ground sloth. It was 30 feet, • Cenozoic Era: current how species originate, have a and lived from 400,000 to 8,000 years and most recent of the 3 range of existence, and go ago in Argentina, Bolivia, and Uruguay. geological eras of the extinct. This issue will complete Phanerozoic Eon; it the DNA activities with are still here and doing well in follows the Mesozoic explorations of how DNA the tropics of South and Central Era 66 MYA to present mutates, and the consequences America! • Eocene: an Epoch in of mutations. the Cenozoic Era from The Cenozoic Era is the Age of 56 to 34 MYA My scientific research is on the Mammals. North America was • Epoch: geologic time mammal group xenarthrans home to many species of saber- within a Period (ground and tree sloths, toothed cats, dire wolves, short- anteaters, armadillos, faced bears, terror birds, CAREER CONNECTION glyptodonts, and pampatheres). -
The Geologic Time Scale Shows Earth's Past
KEY CONCEPT The geologic time scale shows Earth’s past. BEFORE, you learned NOW, you will learn • Rocks and fossils give clues • That Earth is always changing about life on Earth and has always changed in • Layers of sedimentary rocks the past show relative ages • How the geologic time scale • Radioactive dating of igneous describes Earth’s history rocks gives absolute ages VOCABULARY EXPLORE Time Scales uniformitarianism p. 732 How do you make a time scale of your year? geologic time scale p. 733 PROCEDURE MATERIALS • pen 1 Divide your paper into three columns. •sheet of paper 2 In the last column, list six to ten events in the school year in the order they will happen. For example, you may include a particular soccer game or a play. 3 In the middle column, organize those events into larger time periods, such as soccer season, rehearsal week, or whatever you choose. 4 In the first column, organize those time periods into even larger ones. WHAT DO YOU THINK? How does putting events into categories help you to see the relationship among events? Earth is constantly changing. OUTLINE In the late 1700s a Scottish geologist named James Hutton began to Remember to start an question some of the ideas that were then common about Earth and outline in your notebook for this section. how Earth changes. He found fossils and saw them as evidence of life forms that no longer existed. He also noticed that different types of I. Main idea A. Supporting idea fossilized creatures were found in different layers of rocks.