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Diversity Partitioning During the Cambrian Radiation
Diversity partitioning during the Cambrian radiation Lin Naa,1 and Wolfgang Kiesslinga,b aGeoZentrum Nordbayern, Paleobiology and Paleoenvironments, Friedrich-Alexander-Universität Erlangen-Nürnberg, 91054 Erlangen, Germany; and bMuseum für Naturkunde, Leibniz Institute for Research on Evolution and Biodiversity at the Humboldt University Berlin, 10115 Berlin, Germany Edited by Douglas H. Erwin, Smithsonian National Museum of Natural History, Washington, DC, and accepted by the Editorial Board March 10, 2015 (received for review January 2, 2015) The fossil record offers unique insights into the environmental and Results geographic partitioning of biodiversity during global diversifica- Raw gamma diversity exhibits a strong increase in the first three tions. We explored biodiversity patterns during the Cambrian Cambrian stages (informally referred to as early Cambrian in this radiation, the most dramatic radiation in Earth history. We as- work) (Fig. 1A). Gamma diversity dropped in Stage 4 and de- sessed how the overall increase in global diversity was partitioned clined further through the rest of the Cambrian. The pattern is between within-community (alpha) and between-community (beta) robust to sampling standardization (Fig. 1B) and insensitive to components and how beta diversity was partitioned among environ- including or excluding the archaeocyath sponges, which are po- ments and geographic regions. Changes in gamma diversity in the tentially oversplit (16). Alpha and beta diversity increased from Cambrian were chiefly driven by changes in beta diversity. The the Fortunian to Stage 3, and fluctuated erratically through the combined trajectories of alpha and beta diversity during the initial following stages (Fig. 2). Our estimate of alpha (and indirectly diversification suggest low competition and high predation within beta) diversity is based on the number of genera in published communities. -
Living Lakes Goals 2019 - 2024 Achievements 2012 - 2018
Living Lakes Goals 2019 - 2024 Achievements 2012 - 2018 We save the lakes of the world! 1 Living Lakes Goals 2019-2024 | Achievements 2012-2018 Global Nature Fund (GNF) International Foundation for Environment and Nature Fritz-Reichle-Ring 4 78315 Radolfzell, Germany Phone : +49 (0)7732 99 95-0 Editor in charge : Udo Gattenlöhner Fax : +49 (0)7732 99 95-88 Coordination : David Marchetti, Daniel Natzschka, Bettina Schmidt E-Mail : [email protected] Text : Living Lakes members, Thomas Schaefer Visit us : www.globalnature.org Graphic Design : Didem Senturk Photographs : GNF-Archive, Living Lakes members; Jose Carlo Quintos, SCPW (Page 56) Cover photo : Udo Gattenlöhner, Lake Tota-Colombia 2 Living Lakes Goals 2019-2024 | Achievements 2012-2018 AMERICAS AFRICA Living Lakes Canada; Canada ........................................12 Lake Nokoué, Benin .................................................... 38 Columbia River Wetlands; Canada .................................13 Lake Ossa, Cameroon ..................................................39 Lake Chapala; Mexico ..................................................14 Lake Victoria; Kenya, Tanzania, Uganda ........................40 Ignacio Allende Reservoir, Mexico ................................15 Bujagali Falls; Uganda .................................................41 Lake Zapotlán, Mexico .................................................16 I. Lake Kivu; Democratic Republic of the Congo, Rwanda 42 Laguna de Fúquene; Colombia .....................................17 II. Lake Kivu; Democratic -
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. -
Phylogeny and Biogeography of Iguanodontian Dinosaurs, with Implications from Ontogeny and an Examination of the Function of the Fused Carpal-Digit I Complex
Phylogeny and Biogeography of Iguanodontian Dinosaurs, with Implications from Ontogeny and an Examination of the Function of the Fused Carpal-Digit I Complex By Karen E. Poole B.A. in Geology, May 2004, University of Pennsylvania M.A. in Earth and Planetary Sciences, August 2008, Washington University in St. Louis A Dissertation submitted to The Faculty of The Columbian College of Arts and Sciences of The George Washington University in partial fulfillment of the requirements for the degree of Doctor of Philosophy August 31, 2015 Dissertation Directed by Catherine Forster Professor of Biology The Columbian College of Arts and Sciences of The George Washington University certifies that Karen Poole has passed the Final Examination for the degree of Doctor of Philosophy as of August 10th, 2015. This is the final and approved form of the dissertation. Phylogeny and Biogeography of Iguanodontian Dinosaurs, with Implications from Ontogeny and an Examination of the Function of the Fused Carpal-Digit I Complex Karen E. Poole Dissertation Research Committee: Catherine A. Forster, Professor of Biology, Dissertation Director James M. Clark, Ronald Weintraub Professor of Biology, Committee Member R. Alexander Pyron, Robert F. Griggs Assistant Professor of Biology, Committee Member ii © Copyright 2015 by Karen Poole All rights reserved iii Dedication To Joseph Theis, for his unending support, and for always reminding me what matters most in life. To my parents, who have always encouraged me to pursue my dreams, even those they didn’t understand. iv Acknowledgements First, a heartfelt thank you is due to my advisor, Cathy Forster, for giving me free reign in this dissertation, but always providing valuable commentary on any piece of writing I sent her, no matter how messy. -
Dating Dinosaurs
The PRINCETON FIELD GUIDE to DINOSAURS 2ND EDITION PRINCETON FIELD GUIDES Rooted in field experience and scientific study, Princeton’s guides to animals and plants are the authority for professional scientists and amateur naturalists alike. Princeton Field Guides present this information in a compact format carefully designed for easy use in the field. The guides illustrate every species in color and provide detailed information on identification, distribution, and biology. Albatrosses, Petrels, and Shearwaters of the World, by Derek Onley Birds of Southern Africa, Fourth Edition, by Ian Sinclair, Phil and Paul Scofield Hockey, Warwick Tarboton, and Peter Ryan Birds of Aruba, Curaçao, and Bonaire by Bart de Boer, Eric Birds of Thailand, by Craig Robson Newton, and Robin Restall Birds of the West Indies, by Herbert Raffaele, James Wiley, Birds of Australia, Eighth Edition, by Ken Simpson and Nicolas Orlando Garrido, Allan Keith, and Janis Raffaele Day Birds of Western Africa, by Nik Borrow and Ron Demey Birds of Borneo: Brunei, Sabah, Sarawak, and Kalimantan, by Carnivores of the World, by Luke Hunter Susan Myers Caterpillars of Eastern North America: A Guide to Identification Birds of Botswana, by Peter Hancock and Ingrid Weiersbye and Natural History, by David L. Wagner Birds of Central Asia, by Raffael Ayé, Manuel Schweizer, and Common Mosses of the Northeast and Appalachians, by Karl B. Tobias Roth McKnight, Joseph Rohrer, Kirsten McKnight Ward, and Birds of Chile, by Alvaro Jaramillo Warren Perdrizet Birds of the Dominican Republic and Haiti, by Steven Latta, Coral Reef Fishes, by Ewald Lieske and Robert Meyers Christopher Rimmer, Allan Keith, James Wiley, Herbert Dragonflies and Damselflies of the East, by Dennis Paulson Raffaele, Kent McFarland, and Eladio Fernandez Dragonflies and Damselflies of the West, by Dennis Paulson Birds of East Africa: Kenya, Tanzania, Uganda, Rwanda, and Mammals of Europe, by David W. -
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). -
Inferring Body Mass in Extinct Terrestrial Vertebrates and the Evolution of Body Size in a Model-Clade of Dinosaurs (Ornithopoda)
Inferring Body Mass in Extinct Terrestrial Vertebrates and the Evolution of Body Size in a Model-Clade of Dinosaurs (Ornithopoda) by Nicolás Ernesto José Campione Ruben A thesis submitted in conformity with the requirements for the degree of Doctor of Philosophy Ecology and Evolutionary Biology University of Toronto © Copyright by Nicolás Ernesto José Campione Ruben 2013 Inferring body mass in extinct terrestrial vertebrates and the evolution of body size in a model-clade of dinosaurs (Ornithopoda) Nicolás E. J. Campione Ruben Doctor of Philosophy Ecology and Evolutionary Biology University of Toronto 2013 Abstract Organismal body size correlates with almost all aspects of ecology and physiology. As a result, the ability to infer body size in the fossil record offers an opportunity to interpret extinct species within a biological, rather than simply a systematic, context. Various methods have been proposed by which to estimate body mass (the standard measure of body size) that center on two main approaches: volumetric reconstructions and extant scaling. The latter are particularly contentious when applied to extinct terrestrial vertebrates, particularly stem-based taxa for which living relatives are difficult to constrain, such as non-avian dinosaurs and non-therapsid synapsids, resulting in the use of volumetric models that are highly influenced by researcher bias. However, criticisms of scaling models have not been tested within a comprehensive extant dataset. Based on limb measurements of 200 mammals and 47 reptiles, linear models were generated between limb measurements (length and circumference) and body mass to test the hypotheses that phylogenetic history, limb posture, and gait drive the relationship between stylopodial circumference and body mass as critics suggest. -
Orbital Pacing and Secular Evolution of the Early Jurassic Carbon Cycle
Orbital pacing and secular evolution of the Early Jurassic carbon cycle Marisa S. Storma,b,1, Stephen P. Hesselboc,d, Hugh C. Jenkynsb, Micha Ruhlb,e, Clemens V. Ullmannc,d, Weimu Xub,f, Melanie J. Lengg,h, James B. Ridingg, and Olga Gorbanenkob aDepartment of Earth Sciences, Stellenbosch University, 7600 Stellenbosch, South Africa; bDepartment of Earth Sciences, University of Oxford, OX1 3AN Oxford, United Kingdom; cCamborne School of Mines, University of Exeter, TR10 9FE Penryn, United Kingdom; dEnvironment and Sustainability Institute, University of Exeter, TR10 9FE Penryn, United Kingdom; eDepartment of Geology, Trinity College Dublin, The University of Dublin, Dublin 2, Ireland; fDepartment of Botany, Trinity College Dublin, The University of Dublin, Dublin 2, Ireland; gEnvironmental Science Centre, British Geological Survey, NG12 5GG Nottingham, United Kingdom; and hSchool of Biosciences, University of Nottingham, LE12 5RD Loughborough, United Kingdom Edited by Lisa Tauxe, University of California San Diego, La Jolla, CA, and approved January 3, 2020 (received for review July 14, 2019) Global perturbations to the Early Jurassic environment (∼201 to where they are recorded as individual shifts or series of shifts ∼174 Ma), notably during the Triassic–Jurassic transition and Toar- within stratigraphically limited sections. Some of these short-term cian Oceanic Anoxic Event, are well studied and largely associated δ13C excursions have been shown to represent changes in the with volcanogenic greenhouse gas emissions released by large supraregional to global carbon cycle, marked by synchronous igneous provinces. The long-term secular evolution, timing, and changes in δ13C in marine and terrestrial organic and inorganic pacing of changes in the Early Jurassic carbon cycle that provide substrates and recorded on a wide geographic extent (e.g., refs. -
Fluid Escape Structures As Possible Indicators of Past Gas Hydrate
DOI: 10.1590/2317‑4889201720160090 ARTICLE Fluid escape structures as possible indicators of past gas hydrate dissociation during the deposition of the Barremian sediments in the Recôncavo Basin, NE, Brazil Estruturas de escape de fluidos como possíveis indicadoras de uma paleo‑dissociação de hidratos de gás durante a deposição de sedimentos do Barremiano na Bacia do Recôncavo, NE, Brasil Antonio Fernando Menezes Freire1*, Carlson de Matos Maia Leite2, Flávio Miranda de Oliveira2, Márcio Ferreira Guimarães2, Paulo da Silva Milhomem2, Raphael Pietzsch3, Roberto Salvador Francisco d’Ávila4 ABSTRACT: Empty elliptical vesicles are observed in outcrops RESUMO: Vesículas elípticas ocas são observadas em afloramentos de areni- of Barremian very fine clayey sandstone to siltstone lacustrine tos argilosos muito finos e siltitos lacustrinos do Membro Pitanga da Formação slurry deposits of the Pitanga Member (Maracangalha Forma‑ Maracangalha, expostos na Ilha de Maré, sudeste da Bacia do Recôncavo, Es- tion), exposed in the Maré Island, Southern Recôncavo Basin, tado da Bahia, Brasil. Essas rochas foram depositadas em condições subaquo- Brazil. These sedimentary features have been traditionally in‑ sas e são consideradas depósitos gravitacionais do tipo slurry. Essas feições têm terpreted as water escape structures triggered by the diapirism sido tradicionalmente interpretadas como sendo estruturas de escape de água, of the underlying shales of the Candeias Formation. This work resultado da ação do diapismo de folhelhos sotopostos da Formação Candeias. proposes that vesicles were generated during massive gas hydrate Este trabalho propõe que as vesículas foram geradas durante uma intensa dis- dissociation as a result of tectonic activity in a paleolake system. sociação de hidratos de gás em resposta à atividade tectônica existente naquele Tectonic uplift would have triggered both the reduction of the sistema lacustre. -
The Early Jurassic Ornithischian Dinosaurian Ichnogenus Anomoepus
19 The Early Jurassic Ornithischian Dinosaurian Ichnogenus Anomoepus Paul E. Olsen and Emma C. Rainforth nomoepus is an Early Jurassic footprint genus and 19.2). Because skeletons of dinosaur feet were not produced by a relatively small, gracile orni- known at the time, he naturally attributed the foot- A thischian dinosaur. It has a pentadactyl ma- prints to birds. By 1848, however, he recognized that nus and a tetradactyl pes, but only three pedal digits some of the birdlike tracks were associated with im- normally impressed while the animal was walking. The pressions of five-fingered manus, and he gave the name ichnogenus is diagnosed by having the metatarsal- Anomoepus, meaning “unlike foot,” to these birdlike phalangeal pad of digit IV of the pes lying nearly in line with the axis of pedal digit III in walking traces, in combination with a pentadactyl manus. It has a pro- portionally shorter digit III than grallatorid (theropod) tracks, but based on osteometric analysis, Anomoepus, like grallatorids, shows a relatively shorter digit III in larger specimens. Anomoepus is characteristically bi- pedal, but there are quadrupedal trackways and less common sitting traces. The ichnogenus is known from eastern and western North America, Europe, and southern Africa. On the basis of a detailed review of classic and new material, we recognize only the type ichnospecies Anomoepus scambus within eastern North America. Anomoepus is known from many hundreds of specimens, some with remarkable preservation, showing many hitherto unrecognized details of squa- mation and behavior. . Pangea at approximately 200 Ma, showing the In 1836, Edward Hitchcock described the first of what areas producing Anomoepus discussed in this chapter: 1, Newark we now recognize as dinosaur tracks from Early Juras- Supergroup, eastern North America; 2, Karoo basin; 3, Poland; sic Newark Supergroup rift strata of the Connecticut 4, Colorado Plateau. -
Lake Baikal Bibliography, 1989- 1999
UC San Diego Bibliography Title Lake Baikal Bibliography, 1989- 1999 Permalink https://escholarship.org/uc/item/7dc9945d Author Limnological Institute of RAS SB Publication Date 1999-12-31 eScholarship.org Powered by the California Digital Library University of California Lake Baikal Bibliography, 1989- 1999 This is a bibliography of 839 papers published in English in 1989- 1999 by members of Limnological Institute of RAS SB and by their partners within the framework of the Baikal International Center for Ecological Research. Some of the titles are accompanied by abstracts. Coverage is on different aspects of Lake Baikal. Adov F., Takhteev V., Ropstorf P. Mollusks of Baikal-Lena nature reserve (northern Baikal). // World Congress of Malacology: Abstracts; Washington, D.C.: Unitas Malacologica; 1998: 6. Afanasyeva E.L. Life cycle of Epischura baicalensis Sars (Copepoda, Calanoida) in Lake Baikal. // VI International Conference on Copepoda: Abstracts; July 29-August 3, 1996; Oldenburg/Bremerhaven, Germany. Konstanz; 1996: 33. Afanasyeva E.L. Life cycle of Epischura baicalensis Sars (Copepoda, Calanoida) in Lake Baikal. // J. Mar. Syst.; 1998; 15: 351-357. Epischura baicalensis Sars is a dominant pelagic species of Lake Baikal zooplankton. This is endemic to Lake Baikal and inhabits the entire water column. It produces two generations per year: the winter - spring and the summer. These copepods develop under different ecological conditions and vary in the duration of life stages, reproduction time, maturation of sex products and adult males and females lifespan. The total life period of the animals from each generation is one year. One female can produce 10 egg sacks every 10 - 20 days during its life time. -
Universal Studios Pass & Universal Express Pass
UNIVERSAL STUDIOS PASSTM & UNIVERSAL EXPRESSTM PASS UNIVERSAL STUDIOS JAPANTM Booking Period: Now – 31 Mar’18 Admission Date: By 17 May’18 Universal ExpressTM Pass 4 ~Standard~ or Universal ExpressTM Pass 4 ~The Flying Dinosaur~ Wish to maximize your time by skipping the queues at this fun-filled park? With this option, you can enjoy the priority queue at 4 selected rides! Universal ExpressTM Pass 4 Universal ExpressTM Pass 4 ~Standard~ ~The Flying Dinosaur~ Includes Timed Entry into The Wizarding World Includes Timed Entry into The Wizarding World of Harry PotterTM from 10.30am & Express of Harry PotterTM from 11.20am & Express queues for: queues for: **Timed Ride for Harry Potter & the Forbidden JourneyTM is during **Timed Ride for Harry Potter & the Forbidden JourneyTM is during 10.50 – 11.20am only & for Despicable Me Minion Mayhem is 11.40 – 12.10pm only & for Jurassic Park The Flying Dinosaur is during 14.10 – 14.40pm only. during 14.00 – 14.30pm only. **Ride(s) Closure: Terminator 2: 3D® – 10 to 11 Apr / The Amazing Adventures of Spider-Man – The Ride 4K2D – 7 to 13 May / BackdraftTM – 14 to 25 May 2018. Price per Person (in JPY) Adult & Child (4 years & Above) Fr. JPY 5,200 per person Terms and Conditions ① 7 Days advanced purchase (Based on departure date from Singapore). ② NON-REFUNDABALE / NO CHANGES ALLOWED ONCE CONFIRMED. ③ Prices will fluctuate according to demands and subjected to decisions by Universal Studios JapanTM. Price will only be confirmed at the point of booking. ④ Free admission for children from 0 – 3 years old. ⑤ Limited allotments only daily.