The Magazine for Terrarists No 101
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Index INDEX Note: page numbers in italics refer to fi gures, those in bold refer to tables and boxes. abducens nerve 55 activity cycles 499–522 inhibition 485 absorption effi ciency 72 annual patterns 515, 516, 517–22 interactions 485–6 abyssal zone 393 circadian rhythms 505 prey 445 Acanthaster planci (Crown-of-Thorns Starfi sh) diel patterns 499, 500, 501–2, 503–4, reduction 484 579 504–7 aggressive mimicry 428, 432–3 Acanthocybium (Wahoo) 15 light-induced 499, 500, 501–2, 503–4, aggressive resemblance 425–6 Acanthodii 178, 179 505 aglomerular 52 Acanthomorpha 284–8, 289 lunar patterns 507–9 agnathans Acanthopterygii 291–325 seasonal 509–15 gills 59, 60 Atherinomorpha 293–6 semilunar patterns 507–9 osmoregulation 101, 102 characteristics 291–2 supra-annual patterns 515, 516, 517–22 phylogeny 202 distribution 349, 350 tidal patterns 506–7 ventilation 59, 60 jaws 291 see also migration see also hagfi shes; lampreys Mugilomorpha 292–3, 294 adaptive response 106 agnathous fi shes see jawless fi shes pelagic 405 adaptive zones 534 agonistic interactions 83–4, 485–8 Percomorpha 296–325 adenohypophysis 91, 92 chemically mediated 484 pharyngeal jaws 291 adenosine triphosphate (ATP) 57 sound production 461–2 phylogeny 292, 293, 294 adipose fi n 35 visual 479 spines 449, 450 adrenocorticotropic hormone (ACTH) 92 agricultural chemicals 605 Acanthothoraciformes 177 adrianichthyids 295 air breathing 60, 61–2, 62–4 acanthurids 318–19 adult fi shes 153, 154, 155–7 ammonia production 64, 100–1 Acanthuroidei 12, 318–19 death 156–7 amphibious 60 Acanthurus bahianus -
Occasional Papers of the Museum of Zoology University of Michigan Ann Arbor, Michigan University of Michigan Press Vanishing
OCCASIONAL PAPERS OF THE MUSEUM OF ZOOLOGY UNIVERSITY OF MICHIGAN ANN ARBOR,MICHIGAN UNIVERSITYOF MICHIGANPRESS VANISHING AND EXTINCT COLONIES OF TREE SNAILS, LIGUUS PASCIATUX, IN THE VICINITY OF MIAMT, FLORIDA1 BY FRANKN. YOUNG Szib~nittedfor publicatio?~drine 15, 1950 TI-IE once numerous tropical hardwood hamrnocks in the region of Miami, Florida, are rapidly being enveloped or destroyed by the grow- ing mctropolitan and suburban area. With the destruction of these hammocks the colonies of tree snails, Liguus fasciatus, characteristic of this type of vegetational association are doomed to extinction. Many colonies are complctely lost; others are on the verge of extinc- tion and mnst surely disappear in a few more years. In view of this prospect, I believe that the followiilg notes on the location of the ham- mocBs and thcir associated colonies of Ligzcus will be of value to future workers studying the distribution, ecology, or genetics of this group of snails. Thc tree snails of the genus Liguus are colonial only because they are strictly limited to the subtropical jungle-hammocli associes and to subtropical hammock associes with the corresponding clirnax associa- tions of the Florida Keys and the souther11 mainland (see Davis, 1943). Clench and Fairchild (1939) have reviewed the taxonomy of the Florida forms, and the names used in the present paper are largely based 011 their worlr. I11 some instaiiccs I have retained names of variants placed by them ill synonymy. These names express nzore clearly the 1 Colltributioli No. 463 from the Dcpartme~itof Zoology, Indiana University. Prank N. Young Occ. Papers concept of color patterns which I wish to discuss. -
Cleto Sánchez Falcón” Y “M
34 NOVITATES CARIBAEA 4: 34-44, 2011 MATERIAL TIPO DEPOSITADO EN LAS COLECCIONES MALACOLÓGICAS HISTÓRICAS “CLETO SÁNCHEZ FALCÓN” Y “M. L. JAUME” EN SANTIAGO DE CUBA, CUBA Beatriz Lauranzón Meléndez1, David Maceira Filgueira1 y Margarita Moran Zambrano2. 1Centro Oriental de Ecosistemas y Biodiversidad. BIOECO. Santiago de Cuba, Cuba [email protected] 2Museo “Jorge Ramón Cuevas”, Reserva de Biosfera Baconao. Santiago de Cuba, Cuba RESUMEN Fueron revisadas las colecciones malacológicas históricas “Cleto Sánchez Falcón” y “M. L. Jaume”, depositadas en el Museo de Historia Natural “Tomás Romay” y el Museo “Jorge Ramón Cuevas”. De ambas colecciones se copiaron los datos de etiqueta del material tipo. La validez de la información de etiqueta para cada lote fue revisada con las descripciones originales correspondientes a cada especie, revisiones taxonómicas de familias y catálogos actualizados. Se registraron 434 ejemplares, incluidos en 56 subespecies, 34 especies y seis (6) familias; estos se corresponden con 85 localidades y 16 colectores. La colección “Cleto Sánchez Falcón” posee 368 ejemplares de las familias Annulariidae, Cerionidae, Megalomastomidae, Helicinidae, Orthalicidae y Urocoptidae, siendo esta última la más representada. La colección “M. L. Jaume” tiene 66 ejemplares de 36 subespecies de Liguus fasciatus (Müller), Orthalicidae. Palabras clave: moluscos terrestres, material tipo, colección histórica, Cuba. ABSTRACT The historic malacological collections “Cleto Sánchez Falcón” and “M. L. Jaume” housed in the Museo de Historia Natural “Tomás Romay” and Museo “Jorge Ramón Cuevas” were revised, and the label data of type material was copied. The validity of the information on labels for each lot was revised with the original descriptions for all species, taxonomic revisions of families and updated catalogues. -
New Mexico Geological Society 2019 Spring Meeting Abstracts
New Mexico Geological Society 2019 Spring Meeting Abstracts TOWARDS UNDERSTANDING THE have led to a stratigraphic nomenclature that by university and museum geologists is confirma- EFFECTS OF ATMOSPHERIC PRESSURE appears to be applicable over a large area of the tion of the ready recognition and utility of these VARIATIONS ON LONG-PERIOD state, from the Sierra Oscura of Socorro County subdivisions in regional stratigraphy, mapping HORIZONTAL SEISMIC DATA: northward to the Sandia Mountains of Bernalillo and economic geology. A CASE STUDY County, a transect of about 150 km. Thus, Mid- Alexis C. B. Alejandro, Adam T. Ringler, David dle and Upper Pennsylvanian (Atokan-Virgilian) C. Wilson, Robert E. Anthony, marine and marginal-marine strata are assigned AN OVERVIEW OF THE ALBUQUERQUE and Sabrina V. Moore to the Sandia Formation (containing a relative SEISMOLOGICAL LABORATORY AND abundance of siliciclastic deposits), the overlying RECENT ADVANCES IN SEISMIC Incoherent noise generated by seismometer tilt Gray Mesa Formation (dominantly carbonate INSTRUMENTATION caused by atmospheric pressure variations often facies), and the Atrasado Formation (alternating Robert E. Anthony, Adam T. Ringler, limits seismological studies utilizing long-period siliciclastic- and carbonate-dominated intervals). and David C. Wilson (>10 s period), horizontal-component seismic A number of intraformational units (members) records. Several case studies have suggested have been identified, with eight members in the The Albuquerque Seismological Laboratory methodologies for correcting these unwanted Middle-Upper Pennsylvanian Atrasado For- (ASL) was established in 1961 in one of the signals using collocated pressure records. However, mation presently recognized. An uninterrupted seismically quietest regions in the country in it is unclear if these corrections are applicable section of the Pennsylvanian System is exposed in order to test seismometers for what is now the to a variety of different geologic settings and Tijeras Canyon east of Albuquerque, NM, along U.S. -
Florida Tree Snail Species Conservation Measures and Permitting
SPECIES CONSERVATION MEASURES AND PERMITTING GUIDELINES Effective December, 2020 Florida Tree Snail Liguus fasciatus Species Overview Status: Removed from Florida’s Endangered and Threatened Species List. Current Protections • 68A-4.001, F.A.C., General Prohibitions and Photograph by Randy Grau, FWC. Requirement – Prohibits the take, transport, sale, and possession of wildlife. • 68A-1.004, F.A.C., Take – The term take shall include taking, attempting to take, pursuing, hunting, molesting, capturing, or killing any wildlife or freshwater fish, or their nests or eggs by any means whether or not such actions result in obtaining possession of such wildlife or freshwater fish or their nests or eggs. Biological Background This section describes the biological background for this species and provides context for the following sections. It focuses on the habitats that support the Florida tree snail, and the threats faced by the species. Florida tree snails (Liguus fasciatus) have historically been found in Collier, Palm Beach, Broward, Miami-Dade, and Monroe counties (Deisler-Seno 1994). Currently the species is primarily known from Miami-Dade, Monroe, and Collier counties (Emmel and Cotter 1995; see range map). The Florida tree snail has a conical shell 40 to 70 mm (1.6 to 2.7 in) in length. The shell color is extremely variable and can be matte or glossy (Pilsbry 1946). There are 58 named color morphs of the Florida tree snail (Jones et al. 1981, Roth and Bogan 1984, Emmel and Cotter 1995; Figure 1). Research shows very low genetic variation and suggests that all color morphs belong to a single species, Liguus fasciatus (Hillis 1995). -
Vol. 25 No. 1 March, 2000 H a M a D R Y a D V O L 25
NO.1 25 M M A A H D A H O V D A Y C R R L 0 0 0 2 VOL. 25NO.1 MARCH, 2000 2% 3% 2% 3% 2% 3% 2% 3% 2% 3% 2% 3% 2% 3% 2% 3% 2% 3% 4% 5% 4% 5% 4% 5% 4% 5% 4% 5% 4% 5% 4% 5% 4% 5% 4% 5% HAMADRYAD Vol. 25. No. 1. March 2000 Date of issue: 31 March 2000 ISSN 0972-205X Contents A. E. GREER & D. G. BROADLEY. Six characters of systematic importance in the scincid lizard genus Mabuya .............................. 1–12 U. MANTHEY & W. DENZER. Description of a new genus, Hypsicalotes gen. nov. (Sauria: Agamidae) from Mt. Kinabalu, North Borneo, with remarks on the generic identity of Gonocephalus schultzewestrumi Urban, 1999 ................13–20 K. VASUDEVAN & S. K. DUTTA. A new species of Rhacophorus (Anura: Rhacophoridae) from the Western Ghats, India .................21–28 O. S. G. PAUWELS, V. WALLACH, O.-A. LAOHAWAT, C. CHIMSUNCHART, P. DAVID & M. J. COX. Ethnozoology of the “ngoo-how-pak-pet” (Serpentes: Typhlopidae) in southern peninsular Thailand ................29–37 S. K. DUTTA & P. RAY. Microhyla sholigari, a new species of microhylid frog (Anura: Microhylidae) from Karnataka, India ....................38–44 Notes R. VYAS. Notes on distribution and breeding ecology of Geckoella collegalensis (Beddome, 1870) ..................................... 45–46 A. M. BAUER. On the identity of Lacerta tjitja Ljungh 1804, a gecko from Java .....46–49 M. F. AHMED & S. K. DUTTA. First record of Polypedates taeniatus (Boulenger, 1906) from Assam, north-eastern India ...................49–50 N. M. ISHWAR. Melanobatrachus indicus Beddome, 1878, resighted at the Anaimalai Hills, southern India ............................. -
Achatina Fulica Background
Giant African Land Snail, Achatina fulica Background • Originally from coastal East Africa and its islands • Has spread to other parts of Africa, Asia, some Pacific islands, Australia, New Zealand, South America, the Caribbean, and the United States • Can be found in agricultural areas, natural forests, planted forests, riparian zones, wetlands, disturbed areas, and even urban areas in warm tropical climates with high humidity • Also known scientifically as Lissachatina fulica • Common names include giant African land snail and giant African snail Hosts Image citation: Cotton - Charles T. Bryson, USDA Agricultural Research Service, www.bugwood.org, #1116132 Banana - Charles T. Bryson, USDA Agricultural Research Service, www.bugwood.org, #1197011 Papaya - Forest & Kim Starr, Starr Environmental, www.bugwood.org, #5420178 Pumpkin - Howard F. Schwartz, Colorado State University, www.bugwood.org, #5365883 Cucumber - Howard F. Schwartz, Colorado State University, www.bugwood.org., #5363704 Carrots - M.E. Bartolo, www.bugwood.org, #5359190 Environmental Impacts • Consumes large quantities and numbers of species of native plants – May cause indirect damage to plants due to the sheer numbers of snails being so heavy that the plants beak under their weight – May also be a vector of several plant pathogens • Outcompetes and may even eat native snails • It eats so much it can alter the nutrient cycling • Their shells can neutralize acid soils and therefore damage plants that prefer acidic soils • Indirectly, the biocontrol and chemical control that is used on this species can affect native snail species as well. Structural Concerns and Nuisance Issues Image citation: Florida Department of Agriculture and Consumer Services, Division of Plant Industry Public Health Concerns • Intermediate host that vectors: – rat lungworm, Angiostrongylus cantonensis (roundworm) – A. -
MAHS Care Sheet Master List *By Eric Roscoe Care Sheets Are Often An
MAHS Care Sheet Master List *By Eric Roscoe Care sheets are often an excellent starting point for learning more about the biology and husbandry of a given species, including their housing/enclosure requirements, temperament and handling, diet , and other aspects of care. MAHS itself has created many such care sheets for a wide range of reptiles, amphibians, and invertebrates we believe to have straightforward care requirements, and thus make suitable family and beginner’s to intermediate level pets. Some species with much more complex, difficult to meet, or impracticable care requirements than what can be adequately explained in a one page care sheet may be multiple pages. We can also provide additional links, resources, and information on these species we feel are reliable and trustworthy if requested. If you would like to request a copy of a care sheet for any of the species listed below, or have a suggestion for an animal you don’t see on our list, contact us to let us know! Unfortunately, for liability reasons, MAHS is unable to create or publish care sheets for medically significant venomous species. This includes species in the families Crotilidae, Viperidae, and Elapidae, as well as the Helodermatidae (the Gila Monsters and Mexican Beaded Lizards) and some medically significant rear fanged Colubridae. Those that are serious about wishing to learn more about venomous reptile husbandry that cannot be adequately covered in one to three page care sheets should take the time to utilize all available resources by reading books and literature, consulting with, and working with an experienced and knowledgeable mentor in order to learn the ropes hands on. -
How Is the COVID-19 Outbreak Affecting Wildlife Around the World?
Open Journal of Ecology, 2020, 10, 497-517 https://www.scirp.org/journal/oje ISSN Online: 2162-1993 ISSN Print: 2162-1985 How Is the COVID-19 Outbreak Affecting Wildlife around the World? Abdel Fattah N. Abd Rabou Department of Biology, Faculty of Science, Islamic University of Gaza, Gaza Strip, Palestine How to cite this paper: Abd Rabou, A.N. Abstract (2020) How Is the COVID-19 Outbreak Affecting Wildlife around the World? Open The COVID-19 is the infectious disease caused by the most recently discov- Journal of Ecology, 10, 497-517. ered coronavirus at an animal market in Wuhan, China. Many wildlife spe- https://doi.org/10.4236/oje.2020.108032 cies have been suggested as possible intermediate sources for the transmission Received: June 2, 2020 of COVID-19 virus from bats to humans. The quick transmission of COVID-19 Accepted: August 1, 2020 outbreak has imposed quarantine measures across the world, and as a result, Published: August 4, 2020 most of the world’s towns and cities fell silent under lockdowns. The current Copyright © 2020 by author(s) and study comes to investigate the ways by which the COVID-19 outbreak affects Scientific Research Publishing Inc. wildlife globally. Hundreds of internet sites and scientific reports have been This work is licensed under the Creative reviewed to satisfy the needs of the study. Stories of seeing wild animals Commons Attribution International roaming the quiet, deserted streets and cities during the COVID-19 outbreak License (CC BY 4.0). http://creativecommons.org/licenses/by/4.0/ have been posted in the media and social media. -
LITERATURE CITED 90-Day and 12-Month
LITERATURE CITED 90-Day and 12-Month Findings on a Petition to List the Miami Tiger Beetle as an Endangered or Threatened Species; Proposed Endangered Species Status for the Miami Tiger Beetle Docket no.: FWS-R4-ES-2015-0164 Alexander, T.R. 1953. Plant succession of Key Largo, Florida involving Pinus caribaea and Quercus virginiana. Quarterly Journal of Florida Academy of Sciences 16:133–138. Alexander, T.R. 1967. A tropical hammock on the Miami (Florida) limestone—a twenty-five- year study. Ecology 48(5):863-867. Bargar, T.A. 2012. FL – Cholinesterase inhibition in butterflies following aerial broadcast of naled on the National Key Deer Refuge. Interim report to submitted to U.S. Fish and Wildlife Service, Big Pine Key, Florida. Southeast Ecological Science Center, United States Geological Service, Gainesville, Florida. Bartlett, S.N., M.M. McDonough, L.K. Ammerman. 2013. Molecular systematics of bonneted bats (Molossidae: Eumops) based on mitochondrial and nuclear DNA sequences. Journal of Mammalogy 94(4):867–880. Beaumont, L., A. Pitman, S. Perkins, N. Zimmermann, N. Yoccoz, and W. Thuiller. 2011. Impacts of climate change on the world’s most exceptional ecoregions. PNAS 108(6): 2306–2311. Berg, M., E. Kiers, G. Driessen, M. van der Heijden, B. Kooi, F. Kuenen, M. Liefting, H. Verhoef, and J. Ellers. 2009. Adapt or disperse: understanding species persistence in a changing world. Glob. Chg. Biol. doi: 10.1111/j.1365–2486.2009.02014x. Bousquet, Y. 2012. Catalogue of Geadephaga (Coleoptera, Adephaga) of America, north of Mexico. ZooKeys 245:1-1722. Bradley, K.A. and G.D. Gann. -
Integrating Climate Change Vulnerability Assessments Into Adaptation Planning
Integrating climate change vulnerability assessments into adaptation planning A case study using the NatureServe Climate Change Vulnerability Index to inform conservation planning for species in Florida A Report Prepared for the Florida Fish and Wildlife Conservation Commission Natalie Dubois, Astrid Caldas, Judy Boshoven & Aimee Delach Defenders of Wildlife is a national, nonprofit, membership organization dedicated to the protection of all native wild animals and plants in their natural communities. Jamie Rappaport Clark, President Donald Barry, Executive Vice President This report was made possible with the generous support of the Doris Duke Charitable Foundation, the Kresge Foundation and the Educational Foundation of America AUTHORS Natalie Dubois Astrid Caldas Judy Boshoven Aimee Delach With additional input from Amielle DeWan and Kathleen Theoharides PRODUCTION Claire Colegrove © 2011 Defenders of Wildlife, 1130 17th St NW, Washington D.C. 20036 http:/www.defenders.org Disclaimer: This document represents the work and views of the authors and does not necessarily imply endorsement by the Florida Fish and Wildlife Conservation Commission. Suggested citation: Dubois, N., A. Caldas, J. Boshoven, and A. Delach. 2011. Integrating Climate Change Vulnerability Assessments into Adaptation Planning: A Case Study Using the NatureServe Climate Change Vulnerability Index to Inform Conservation Planning for Species in Florida [Final Report]. Defenders of Wildlife, Washington D.C. CONTENTS Executive Summary ................................................................................... -
Downloaded from NCBI Genbank (Benson Et Al
THE UNIVERSITY OF CHICAGO EVOLUTION IN FRESH WATERS DURING THE GREAT AMERICAN INTERCHANGE A DISSERTATION SUBMITTED TO THE FACULTY OF THE DIVISION OF THE BIOLOGICAL SCIENCES AND THE PRITZKER SCHOOL OF MEDICINE IN CANDIDACY FOR THE DEGREE OF DOCTOR OF PHILOSOPHY COMMITTEE ON EVOLUTIONARY BIOLOGY BY TIMOTHY SOSA CHICAGO, ILLINOIS DECEMBER 2017 Table of Contents List of Tables . iii List of Figures . iv Acknowledgments . vi Chapter 1: Introduction . 1 Chapter 2: Broadly sampled phylogeny of Characiformes reveals repeated colonization of North America and paraphyly of Characiformes sensu stricto . 8 Chapter 3: No evidence for filtering of eco-morphology in characiform lineages during the Great American Interchange . 17 Chapter 4: Both elevation and species identity strongly predict body shape in Astyanax tetras . 27 Chapter 5: Diet may mediate potential range expansions of Neotropical fishes under climate change . 39 Chapter 6: Discussion . 52 References . 57 Appendix: List of specimens newly sequenced for this study . 67 ii List of Tables 1.1 Recognized families in the order Characiformes . 5 2.1 Fossil occurrences used for time-calibration . 11 4.1 Distances in morphospace among tetra populations . 32 5.1 Variables determining the range limits of Astyanax . 45 5.2 Variables determining the range limits of Brycon . 47 5.3 Variables determining the range limits of Roeboides . 49 iii List of Figures 1.1 Hypothetical relationships among ostariophysan groups . 4 2.1 Phylogeny of Characiformes as inferred from myh6 locus . 13 3.1 Landmark configuration for geometric morphometrics . 19 3.2 Morphospace occupation in North and South American characins . 21 3.3 Deformation grids showing axes of shape variation among characins .