Animals of Instagram: Taxonomic Bias in Science Communication Online’
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Freshwater Fishes
WESTERN CAPE PROVINCE state oF BIODIVERSITY 2007 TABLE OF CONTENTS Chapter 1 Introduction 2 Chapter 2 Methods 17 Chapter 3 Freshwater fishes 18 Chapter 4 Amphibians 36 Chapter 5 Reptiles 55 Chapter 6 Mammals 75 Chapter 7 Avifauna 89 Chapter 8 Flora & Vegetation 112 Chapter 9 Land and Protected Areas 139 Chapter 10 Status of River Health 159 Cover page photographs by Andrew Turner (CapeNature), Roger Bills (SAIAB) & Wicus Leeuwner. ISBN 978-0-620-39289-1 SCIENTIFIC SERVICES 2 Western Cape Province State of Biodiversity 2007 CHAPTER 1 INTRODUCTION Andrew Turner [email protected] 1 “We live at a historic moment, a time in which the world’s biological diversity is being rapidly destroyed. The present geological period has more species than any other, yet the current rate of extinction of species is greater now than at any time in the past. Ecosystems and communities are being degraded and destroyed, and species are being driven to extinction. The species that persist are losing genetic variation as the number of individuals in populations shrinks, unique populations and subspecies are destroyed, and remaining populations become increasingly isolated from one another. The cause of this loss of biological diversity at all levels is the range of human activity that alters and destroys natural habitats to suit human needs.” (Primack, 2002). CapeNature launched its State of Biodiversity Programme (SoBP) to assess and monitor the state of biodiversity in the Western Cape in 1999. This programme delivered its first report in 2002 and these reports are updated every five years. The current report (2007) reports on the changes to the state of vertebrate biodiversity and land under conservation usage. -
Misgund Orchards
MISGUND ORCHARDS ENVIRONMENTAL AUDIT 2014 Grey Rhebok Pelea capreolus Prepared for Mr Wayne Baldie By Language of the Wilderness Foundation Trust In March 2002 a baseline environmental audit was completed by Conservation Management Services. This foundational document has served its purpose. The two (2) recommendations have been addressed namely; a ‘black wattle control plan’ in conjunction with Working for Water Alien Eradication Programme and a survey of the fish within the rivers was also addressed. Furthermore updated species lists have resulted (based on observations and studies undertaken within the region). The results of these efforts have highlighted the significance of the farm Misgund Orchards and the surrounds, within the context of very special and important biodiversity. Misgund Orchards prides itself with a long history of fruit farming excellence, and has strived to ensure a healthy balance between agricultural priorities and our environment. Misgund Orchards recognises the need for a more holistic and co-operative regional approach towards our environment and needs to adapt and design a more sustainable approach. The context of Misgund Orchards is significant, straddling the protected areas Formosa Forest Reserve (Niekerksberg) and the Baviaanskloof Mega Reserve. A formidable mountain wilderness with World Heritage Status and a Global Biodiversity Hotspot (See Map 1 overleaf). Rhombic egg eater Dasypeltis scabra MISGUND ORCHARDS Langkloof Catchment MAP 1 The regional context of Misgund Orchards becomes very apparent, where the obvious strategic opportunity exists towards creating a bridge of corridors linking the two mountain ranges Tsitsikamma and Kouga (south to north). The environmental significance of this cannot be overstated – essentially creating a protected area from the ocean into the desert of the Klein-karoo, a traverse of 8 biomes, a veritable ‘garden of Eden’. -
TNP SOK 2011 Internet
GARDEN ROUTE NATIONAL PARK : THE TSITSIKAMMA SANP ARKS SECTION STATE OF KNOWLEDGE Contributors: N. Hanekom 1, R.M. Randall 1, D. Bower, A. Riley 2 and N. Kruger 1 1 SANParks Scientific Services, Garden Route (Rondevlei Office), PO Box 176, Sedgefield, 6573 2 Knysna National Lakes Area, P.O. Box 314, Knysna, 6570 Most recent update: 10 May 2012 Disclaimer This report has been produced by SANParks to summarise information available on a specific conservation area. Production of the report, in either hard copy or electronic format, does not signify that: the referenced information necessarily reflect the views and policies of SANParks; the referenced information is either correct or accurate; SANParks retains copies of the referenced documents; SANParks will provide second parties with copies of the referenced documents. This standpoint has the premise that (i) reproduction of copywrited material is illegal, (ii) copying of unpublished reports and data produced by an external scientist without the author’s permission is unethical, and (iii) dissemination of unreviewed data or draft documentation is potentially misleading and hence illogical. This report should be cited as: Hanekom N., Randall R.M., Bower, D., Riley, A. & Kruger, N. 2012. Garden Route National Park: The Tsitsikamma Section – State of Knowledge. South African National Parks. TABLE OF CONTENTS 1. INTRODUCTION ...............................................................................................................2 2. ACCOUNT OF AREA........................................................................................................2 -
The Head of Xenopus Laevls. by Nellie F
The Head of Xenopus laevls. By Nellie F. Paterson, D.Se., Ph.D., Department of Zoology, University of the Witwatersrand, Johannesburg. With Plates 9 to 16. CONTENTS. PAGE INTRODUCTION 161 LATERAL LINE SENSORY ORGANS 163 MUSCULATURE 165 BLOOD-VESSELS ......... 172 THE CHONDROCRANIUM ........ 175 1. Metamorphosis ........ 183 2. Olfactory Eegion 188 3. Nasal Cavities 191 4. Auditory Eegion ........ 193 THE HYOBRANCHIAL SKELETON ....... 196 THE CRANIAL NERVES 198 Ganglion Pro-oticum ........ 199 Nervus Trigeminus ........ 200 1. Ramus Mandibularis 200 2. Ramus Ophthalmicus Profundus 203 NERVUS FACIALIS 209 1. Truncus Supra-orbitalis 210 2. Ramus Hyomandibularis . • - .211 3. Ramus Palatinus ........ 214 NERVI GLOSSOFHARYNGEtTS AND VAGUS . - .216 1. Nervus Glossopharyngeus . • • • .217 2. Nervus Vagus 220 SUMMARY OF COMPOSITION AND DISTRIBUTION OF NERVES . 226 SUMMARY 227 REFERENCES 228 INTRODUCTION. THE Aglossa, comprising only the genera Xenopus, Pipa, Propipa, Hymenochirus, and Pseudohymeno- chirus, are characterized among other things by the absence of a tongue and by a pectoral girdle that exhibits considerable deviation from that of typical Anura Phaneroglossa. NO. 322 M 162 NELLIE F. PATBESON The Aglossa are usually classified as the lowest of the A n u r a, but as Gadow in his account of the Amphibia in the ' Cambridge Natural History' (1909) indicates, their characteristic features are not necessarily primitive ones. A tongue is lacking in the majority of truly aquatic forms, and in the Aglossa the shoulder girdle and other parts of the body are doubtless specialized in response to their particular habits. It is therefore not surprising to find that the Aglossa present some striking morphological similarities with the aquatic Urodela on the one hand, and with certain genera of the Phaneroglossa on the other, but it is very doubtful if these resemblances are of any conse- quence. -
BOA5.1-2 Frog Biology, Taxonomy and Biodiversity
The Biology of Amphibians Agnes Scott College Mark Mandica Executive Director The Amphibian Foundation [email protected] 678 379 TOAD (8623) Phyllomedusidae: Agalychnis annae 5.1-2: Frog Biology, Taxonomy & Biodiversity Part 2, Neobatrachia Hylidae: Dendropsophus ebraccatus CLassification of Order: Anura † Triadobatrachus Ascaphidae Leiopelmatidae Bombinatoridae Alytidae (Discoglossidae) Pipidae Rhynophrynidae Scaphiopopidae Pelodytidae Megophryidae Pelobatidae Heleophrynidae Nasikabatrachidae Sooglossidae Calyptocephalellidae Myobatrachidae Alsodidae Batrachylidae Bufonidae Ceratophryidae Cycloramphidae Hemiphractidae Hylodidae Leptodactylidae Odontophrynidae Rhinodermatidae Telmatobiidae Allophrynidae Centrolenidae Hylidae Dendrobatidae Brachycephalidae Ceuthomantidae Craugastoridae Eleutherodactylidae Strabomantidae Arthroleptidae Hyperoliidae Breviceptidae Hemisotidae Microhylidae Ceratobatrachidae Conrauidae Micrixalidae Nyctibatrachidae Petropedetidae Phrynobatrachidae Ptychadenidae Ranidae Ranixalidae Dicroglossidae Pyxicephalidae Rhacophoridae Mantellidae A B † 3 † † † Actinopterygian Coelacanth, Tetrapodomorpha †Amniota *Gerobatrachus (Ray-fin Fishes) Lungfish (stem-tetrapods) (Reptiles, Mammals)Lepospondyls † (’frogomander’) Eocaecilia GymnophionaKaraurus Caudata Triadobatrachus 2 Anura Sub Orders Super Families (including Apoda Urodela Prosalirus †) 1 Archaeobatrachia A Hyloidea 2 Mesobatrachia B Ranoidea 1 Anura Salientia 3 Neobatrachia Batrachia Lissamphibia *Gerobatrachus may be the sister taxon Salientia Temnospondyls -
Mgr. Jiří Brůna
Přírodovědecká fakulta Masarykovy univerzity Ústav botaniky a zoologie Kotlářská 2 Brno CZ - 61137 MORFOLOGIE A MYOLOGIE POUŠTNÍCH FOREM ŽAB RODU BREVICEPS (ANURA, BREVICIPITIDAE) S OHLEDEM NA JEJICH FYLOGENETICKÉ VZTAHY RIGORÓZNÍ PRÁCE Mgr. Jiří Brůna BRNO 2007 Prohlašuji, že jsem uvedenou práci vypracoval samostatně, jen s použitím citované literatury. ........................................ V Brně dne 15.5. 2007 Jiří Brůna BRŮNA J. 2007. External morphology and myology of the desert forms of Breviceps (Anura, Brevicipitidae) with comments to their phylogenetic relationship. Rigorous thesis. Masaryk University, Brno: 82 pp. Anotace: The phylogenetic relationships of brevicipitid frogs are poorly understood. The first morphology phylogeny for genus Breviceps is presented, including representatives of 8 species (n= 84), and 1 hemisotid genus Hemisus (n=4) as outgroup. The total of 25 morphological characters (synapomorphies) were analysed using Maximum parsimony method - Paup 4.010b. Analysis of the data are consistent with the paraphyly of the Breviceps and forms two sister clades within the genus. Well supported is a monophyly of the clade B. namaquensis and B. macrops grouped with B. rosei as a sister taxon. This group forms a sister clade to the B. gibbosus, B. fuscus and B. verrucosus monophyletic group. Other two species B. adspersus and B. montanus forms a sister clade to this second group. Morphometric study (diameter of the eye) is also described. Breviceps namaquensis and B. macrops possess the biggest eye diameter of the genus and also their six morphological adaptations are presented in this study. Keywords: Anura, Brevicipitidae, Breviceps, morphology, myology, phylogeny, adaptations Touto cestou bych chtěl poděkovat prof. Channingovi (University of the Western Cape, JAR) za poskytnutí zázemí, materiálu a laboratorní techniky včetně cenných rad v průběhu dlouhodobých stáží v Jihoafrické republice (2002-2005). -
Some Aspects of the Anatomy of Anura (Amphibia)-A Review*
SOME ASPECTS OF THE ANATOMY OF ANURA (AMPHIBIA)-A REVIEW* BY L. S. RAMASWAMI (From the Department of Zoology, University of Mysore, Central College, Bangalore) Received July 15, 1939 (Communicated by Prof. A. Subba Rau, D.so., F.R.M.s.) CONTENTS PAGE I. Introduction .. .. .. .. 42 II. Literature Selected .. .. .. .. .. 45 III. Review :- (a) Narial Region .. •. .. .. .. 45 (b) Prechoanal Sac .. •. .. .. .. 47 (c) Septomaxilla .. .. .. .. .. 48 (d) Eminentia Olfactoria .. .. .. .. 49 (e) Sphenethmoid .. .. .. .. .. 50 (f) Subethmoidal Cartilage .. .. .. .. 50 (g) Maxillae .. .. .. .. .. 51 (h) Prevomer .. .. .. .. .. 52 (i) Palatine Bone .. .. .. .. .. 56 (j) The Nasal, Frontoparietal, Squamosal, Pterygoid, Quadratojugal and Parasphenoid Bones .. .. 58 IV. The Middle Far Region .. .. .. .. 60 V. The Pterygoquadrate and its Attachments, and the Arteria Carotis Interna .. .. .. .. .. 63 VI. Bursa Angularis Oris (Fuchs) or the Mundwinkeldruse .. 65 VII. The Lower Jaw .. .. .. .. .. 66 VIII. The Hyolaryngeal Apparatus of Microhylidee and Pelobatidae 66 IX. The Vertebral Column .. .. •. .. .. 68 X. Summary and Conclusions .. .. .. .. 71 XI. Acknowledgement .. .. .. .. .. 76 XII. Bibliography .. .. .. .. .. 77 XIII. Errata List .. .. .. .. .. 80 * Based on the published papers of the author and accepted for the Doctor of Science Degree of the University of Madras, March 1938. 41 B3 F 42 L. S. Ramaswami I. Introduction AT the outset, it must be pointed out that under the title of anatomical studies of Indian and some extrapeninsular Anura, I have examined the cranium and larynx by the method of sections and also by gross study, and the morphological features of the vertebral column of some Indian anuran species by the latter method. It may be remarked here, that the study of cranial morphology by the method of sections revived at the incentive, given by Dr. -
The Histology of Dermal Glands of Mating Breviceps with Comments on Their Possible Functional Value in Microhylids (Amphibia: Anura)
The histology of dermal glands of mating Breviceps with comments on their possible functional value in microhylids (Amphibia: Anura) J. Visser, J.M. Cei and L.S. Gutierrez Department of Zoology, University of Natal, Pietermaritzburg and Universidad Nacional de Cuyo, Mendoza During mating male and female Breviceps become ‘glued’ During mating the male and female Breviceps become together. The distribution of multicellular dermal glands varies ‘glued’ together before, during and for an unknown between the sexes. The male has a large number of holocrine period after oviposition. The animals cannot be glands on the ventrum, while the female has similar glands on the dorsum of the back. It thus appears that both sexes con separated without tearing the adhering skin. This tribute to the ‘glueing’ mechanism. New hypotheses to explain preliminary study reports on the histological sex dif the adhesion between the sexes are proposed, viz., that the ferences of the skin of the mating animals and discusses shift to terrestrial habits and subterranean laying in Breviceps the functional significance of mating adhesion to both have secondarily resulted in male size diminution. In other terrestrial and aquatic breeding microhylids. microhylids which adhere during aquatic oviposition, yet demonstrate a terrestrial morphology and habits, bouyancy is suggested to be of primary functional value. Materials and Methods S. Afr. J. Zool. 1982, 17: 24-27 Several Breviceps gibbosus, collected at Rondebosch, were sent by air from Cape Town to Mendoza in October Tydens paring raak die manlike en vroulike diere aan mekaar 1971. On arrival in Argentine, some pairs were found ‘vasgeplak’. Die verspreiding van multisellulere velkliere verskil ‘glued’ together. -
Reevolution of Lost Mandibular Teeth in Frogs
ORIGINAL ARTICLE doi:10.1111/j.1558-5646.2011.01221.x RE-EVOLUTION OF LOST MANDIBULAR TEETH IN FROGS AFTER MORE THAN 200 MILLION YEARS, AND RE-EVALUATING DOLLO’S LAW John J. Wiens Department of Ecology and Evolution, Stony Brook University, Stony Brook, NY 11794-5245 E-mail: [email protected] Received June 24, 2010 Accepted December 7, 2010 Dollo’s law states that structures that are evolutionarily lost will not be regained. Recent phylogenetic studies have revealed several potential examples in which Dollo’s law seems to be violated, where lost structures appear to have been regained over evolutionary time. However, these examples have recently been questioned and suggested to be methodological artifacts. In this article, I document a striking and incontrovertible phylogenetic example of the re-evolution of a lost, complex structure: mandibular teeth in the frog genus Gastrotheca. I use a time-calibrated phylogeny for 170 amphibian species to show that mandibular teeth were lost in the ancestor of modern frogs at least 230 million years ago (Mya) and have been regained in the last ∼5–17 My. I review recent studies on trait re-evolution and show that this long period of trait absence prior to re-acquisition is largely unprecedented. I also argue that there are several methodological issues that may cause trait re-evolution to be hardest to detect under those conditions when it is most likely to occur, leading to erroneous failures to reject Dollo’s law. Finally, I discuss a mechanism that may facilitate trait re-evolution, and the evolution of mandibular teeth in frogs as an example of developmental constraint. -
Southern African Frogs
AFRICAN SNAKEBITE INSTITUTE – Johan Marais Checklist: Southern African Frogs Scientific Name Common Name Afrikaans Common Name Afrixalus aureus Golden Leaf-folding Frog Goueblaarvoupadda Afrixalus crotalus Snoring Leaf-folding Frog Snorkblaarvoupadda Afrixalus delicatus Delicate Leaf-folding Frog Delikate Blaarvoupadda Afrixalus fornasinii Greater Leaf-folding Frog Grootblaarvoupadda Afrixalus knysnae Knysna Leaf-folding Frog Knysna-blaarvoupadda Afrixalus spinifrons Natal Leaf-folding Frog Natalse Blaarvoupadda Amietia fuscigula Cape River Frog Kaapse Rivierpadda Amietia inyangae Inyanga River Frog Inyanga-rivierpadda Amietia poyntoni Poynton’s River Frog Poynton se Rivierpadda Amietia quecketti Queckett’s River Frog Queckett se Rivierpadda Amietia umbraculata Maluti River Frog Maluti Rivierpadda Amietia vandijki Van Dijk's River Frog Van Dijk se Rivierpadda Amietia vertebralis Phofung River Frog Phofung Rivierpadda Amietophrynus garmani Eastern Olive Toad Olyfskurwepadda Amietophrynus gutturalis Guttural Toad Gorrelskurwepadda Amietophrynus lemairii Lemaire's Toad Lemaire se Skurwepadda Amietophrynus maculatus Flat-backed Toad Gestreepte Skurwepadda Amietophrynus pantherinus Western Leopard Toad Westelike Luiperdskurwepadda Amietophrynus pardalis Eastern Leopard Toad Oostelike Luiperdskurwepadda Amietophrynus poweri Western Olive Toad Power se Skurwepadda Amietophrynus rangeri Raucous Toad Lawaaiskurwepadda Anhydrophryne hewitti Natal Chirping Frog Natalse Kwetterpadda Anhydrophryne ngongoniensis Mistbelt Chirping Frog Misbeltkwetterpadda -
A Previously Unrecognized Radiation of Ranid Frogs in Southern Africa Revealed by Nuclear and Mitochondrial DNA Sequences
Molecular Phylogenetics and Evolution 37 (2005) 674–685 www.elsevier.com/locate/ympev A previously unrecognized radiation of ranid frogs in Southern Africa revealed by nuclear and mitochondrial DNA sequences Arie van der Meijden a, Miguel Vences b, Simone Hoegg a, Axel Meyer a,¤ a Lehrstuhl für Zoologie und Evolutionsbiologie, Department of Biology, University of Konstanz, 78457 Konstanz, Germany b Institute for Biodiversity and Ecosystem Dynamics, Zoological Museum, University of Amsterdam, Mauritskade 61, 1092 AD Amsterdam, The Netherlands Received 17 January 2005; revised 1 May 2005 Available online 21 June 2005 Abstract In sub-Saharan Africa, amphibians are represented by a large number of endemic frog genera and species of incompletely clari- Wed phylogenetic relationships. This applies especially to African frogs of the family Ranidae. We provide a molecular phylogenetic hypothesis for ranids, including 11 of the 12 African endemic genera. Analysis of nuclear (rag-1, rag-2, and rhodopsin genes) and mitochondrial markers (12S and 16S ribosomal RNA genes) provide evidence for an endemic clade of African genera of high mor- phological and ecological diversity thus far assigned to up to Wve diVerent subfamilies: Afrana, Cacosternum, Natalobatrachus, Pyxi- cephalus, Strongylopus, and Tomopterna. This clade has its highest species diversity in southern Africa, suggesting a possible biogeographic connection with the Cape Floral Region. Bayesian estimates of divergence times place the initial diversiWcation of the southern African ranid clade at »62–85 million years ago, concurrent with the onset of the radiation of Afrotherian mammals. These and other African ranids (Conraua, Petropedetes, Phrynobatrachus, and Ptychadena) are placed basally within the Ranoidae with respect to the Eurasian groups, which suggests an African origin for this whole epifamily. -
Raquel Garcia.Pdf
UNCERTAINTY IN PROJECTED IMPACTS OF CLIMATE CHANGE ON BIODIVERSITY A FOCUS ON AFRICAN VERTEBRATES RAQUEL A. GARCIA University of Copenhagen | 2014 Uncertainty in projected impacts of climate change on biodiversity A focus on African vertebrates Raquel A. Garcia PhD thesis | January 2014 University of Copenhagen | Faculty of Science ACADEMIC ADVISORS Prof Miguel B. Araújo CMEC, University of Copenhagen, Denmark Imperial College, Silwood Park, UK National Museum of Natural History–CSIC, Spain InBio/CIBIO, Évora University, Portugal Dr Mar Cabeza Metapopulation Research Group, University of Helsinki, Finland SUBMITTED TO The PhD School of The Faculty of Science, University of Copenhagen, Denmark January 2014 ASSESSMENT COMMITTEE Prof Jane Hill University of York, Department of Biology, UK Dr Richard Pearson University College London, Research Department of Genetics, Evolution and Environment, UK Dr David Nogués-Bravo CMEC, University of Copenhagen, Denmark COPYRIGHT © 2014 Raquel A. Garcia (Synopsis, Design) © 2012 Blackwell Publishing Ltd (Chapter I) © 2014 The Authors Journal of Biogeography Published by John Wiley & Sons Ltd (Chapter II) © 2014 The Authors (Chapter III) © 2014 The Authors (Chapter IV) © 2014 The Authors (Chapter V) Contents | iii Contents Preface v Summary / Resumé vii Acknowledgements x Synopsis 1 The uncertain nature of assessments under climate change 5 Variation in data and model decisions 9 Robustness to ecological assumptions 11 Broadening the scope of assessments 13 Embracing uncertainty 15 References 18 Chapter