British Herpetological Society Bulletin
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Other Contributions
Other Contributions NATURE NOTES Amphibia: Caudata Ambystoma ordinarium. Predation by a Black-necked Gartersnake (Thamnophis cyrtopsis). The Michoacán Stream Salamander (Ambystoma ordinarium) is a facultatively paedomorphic ambystomatid species. Paedomorphic adults and larvae are found in montane streams, while metamorphic adults are terrestrial, remaining near natal streams (Ruiz-Martínez et al., 2014). Streams inhabited by this species are immersed in pine, pine-oak, and fir for- ests in the central part of the Trans-Mexican Volcanic Belt (Luna-Vega et al., 2007). All known localities where A. ordinarium has been recorded are situated between the vicinity of Lake Patzcuaro in the north-central portion of the state of Michoacan and Tianguistenco in the western part of the state of México (Ruiz-Martínez et al., 2014). This species is considered Endangered by the IUCN (IUCN, 2015), is protected by the government of Mexico, under the category Pr (special protection) (AmphibiaWeb; accessed 1April 2016), and Wilson et al. (2013) scored it at the upper end of the medium vulnerability level. Data available on the life history and biology of A. ordinarium is restricted to the species description (Taylor, 1940), distribution (Shaffer, 1984; Anderson and Worthington, 1971), diet composition (Alvarado-Díaz et al., 2002), phylogeny (Weisrock et al., 2006) and the effect of habitat quality on diet diversity (Ruiz-Martínez et al., 2014). We did not find predation records on this species in the literature, and in this note we present information on a predation attack on an adult neotenic A. ordinarium by a Thamnophis cyrtopsis. On 13 July 2010 at 1300 h, while conducting an ecological study of A. -
Approved Plant List 10/04/12
FLORIDA The best time to plant a tree is 20 years ago, the second best time to plant a tree is today. City of Sunrise Approved Plant List 10/04/12 Appendix A 10/4/12 APPROVED PLANT LIST FOR SINGLE FAMILY HOMES SG xx Slow Growing “xx” = minimum height in Small Mature tree height of less than 20 feet at time of planting feet OH Trees adjacent to overhead power lines Medium Mature tree height of between 21 – 40 feet U Trees within Utility Easements Large Mature tree height greater than 41 N Not acceptable for use as a replacement feet * Native Florida Species Varies Mature tree height depends on variety Mature size information based on Betrock’s Florida Landscape Plants Published 2001 GROUP “A” TREES Common Name Botanical Name Uses Mature Tree Size Avocado Persea Americana L Bahama Strongbark Bourreria orata * U, SG 6 S Bald Cypress Taxodium distichum * L Black Olive Shady Bucida buceras ‘Shady Lady’ L Lady Black Olive Bucida buceras L Brazil Beautyleaf Calophyllum brasiliense L Blolly Guapira discolor* M Bridalveil Tree Caesalpinia granadillo M Bulnesia Bulnesia arboria M Cinnecord Acacia choriophylla * U, SG 6 S Group ‘A’ Plant List for Single Family Homes Common Name Botanical Name Uses Mature Tree Size Citrus: Lemon, Citrus spp. OH S (except orange, Lime ect. Grapefruit) Citrus: Grapefruit Citrus paradisi M Trees Copperpod Peltophorum pterocarpum L Fiddlewood Citharexylum fruticosum * U, SG 8 S Floss Silk Tree Chorisia speciosa L Golden – Shower Cassia fistula L Green Buttonwood Conocarpus erectus * L Gumbo Limbo Bursera simaruba * L -
Xenosaurus Tzacualtipantecus. the Zacualtipán Knob-Scaled Lizard Is Endemic to the Sierra Madre Oriental of Eastern Mexico
Xenosaurus tzacualtipantecus. The Zacualtipán knob-scaled lizard is endemic to the Sierra Madre Oriental of eastern Mexico. This medium-large lizard (female holotype measures 188 mm in total length) is known only from the vicinity of the type locality in eastern Hidalgo, at an elevation of 1,900 m in pine-oak forest, and a nearby locality at 2,000 m in northern Veracruz (Woolrich- Piña and Smith 2012). Xenosaurus tzacualtipantecus is thought to belong to the northern clade of the genus, which also contains X. newmanorum and X. platyceps (Bhullar 2011). As with its congeners, X. tzacualtipantecus is an inhabitant of crevices in limestone rocks. This species consumes beetles and lepidopteran larvae and gives birth to living young. The habitat of this lizard in the vicinity of the type locality is being deforested, and people in nearby towns have created an open garbage dump in this area. We determined its EVS as 17, in the middle of the high vulnerability category (see text for explanation), and its status by the IUCN and SEMAR- NAT presently are undetermined. This newly described endemic species is one of nine known species in the monogeneric family Xenosauridae, which is endemic to northern Mesoamerica (Mexico from Tamaulipas to Chiapas and into the montane portions of Alta Verapaz, Guatemala). All but one of these nine species is endemic to Mexico. Photo by Christian Berriozabal-Islas. amphibian-reptile-conservation.org 01 June 2013 | Volume 7 | Number 1 | e61 Copyright: © 2013 Wilson et al. This is an open-access article distributed under the terms of the Creative Com- mons Attribution–NonCommercial–NoDerivs 3.0 Unported License, which permits unrestricted use for non-com- Amphibian & Reptile Conservation 7(1): 1–47. -
A Conservation Framework for the Critically Endangered Endemic Species of the Caribbean Palm Coccothrinax
A conservation framework for the Critically Endangered endemic species of the Caribbean palm Coccothrinax B RETT J ESTROW,BRÍGIDO P EGUERO,FRANCISCO J IMÉNEZ,RAÚL V ERDECIA L ISBET G ONZÁLEZ-OLIVA,CELIO E. MOYA,WILLIAM C INEA,M.PATRICK G RIFFITH A LAN W. MEEROW,MIKE M AUNDER and J AVIER F RANCISCO-ORTEGA Abstract With threatened species ( categorized as plant exploration initiatives, taxonomic revisions, outreach, Critically Endangered and as Endangered, sensu IUCN), and fundraising. The ultimate aim of this review is to provide Coccothrinax (c. species) is the flagship palm genus for baseline information that will develop conservation synergy conservation in the Caribbean Island Biodiversity Hotspot. among relevant parties working on Coccothrinax conserva- Coccothrinax has its centre of taxonomic diversity in these tion in Cuba, Haiti and the Dominican Republic. Such colla- islands, with c. endemic species. We present a conservation borations could also benefit through partnerships with framework for the Critically Endangered species, found botanists working in other countries. in Cuba, Haiti or the Dominican Republic. Only two species Keywords Antilles, Arecaceae, IUCN, plant biodiversity, (C. jimenezii, C. montana) occur in more than one country red lists, taxonomy, tropical islands (Haiti and the Dominican Republic). Immediate threats include oil drilling and nickel mining, intrusion of saline water into soil, urban and agricultural development, low population recruitment, uncontrolled fires, interspecific hy- Introduction bridization, and unsustainable ethnobotanical practices. Coccothrinax bermudezii, C. borhidiana, C. crinita ssp. crini- alms are an iconic feature of the Caribbean landscape ta, C. leonis and C. spissa are not conserved in protected areas. Pand are associated with strong folk and ethnobotani- Coccothrinax bermudezii, C. -
Belize), and Distribution in Yucatan
University of Neuchâtel, Switzerland Institut of Zoology Ecology of the Black Catbird, Melanoptila glabrirostris, at Shipstern Nature Reserve (Belize), and distribution in Yucatan. J.Laesser Annick Morgenthaler May 2003 Master thesis supervised by Prof. Claude Mermod and Dr. Louis-Félix Bersier CONTENTS INTRODUCTION 1. Aim and description of the study 2. Geographic setting 2.1. Yucatan peninsula 2.2. Belize 2.3. Shipstern Nature Reserve 2.3.1. History and previous studies 2.3.2. Climate 2.3.3. Geology and soils 2.3.4. Vegetation 2.3.5. Fauna 3. The Black Catbird 3.1. Taxonomy 3.2. Description 3.3. Breeding 3.4. Ecology and biology 3.5. Distribution and threats 3.6. Current protection measures FIRST PART: BIOLOGY, HABITAT AND DENSITY AT SHIPSTERN 4. Materials and methods 4.1. Census 4.1.1. Territory mapping 4.1.2. Transect point-count 4.2. Sizing and ringing 4.3. Nest survey (from hide) 5. Results 5.1. Biology 5.1.1. Morphometry 5.1.2. Nesting 5.1.3. Diet 5.1.4. Competition and predation 5.2. Habitat use and population density 5.2.1. Population density 5.2.2. Habitat use 5.2.3. Banded individuals monitoring 5.2.4. Distribution through the Reserve 6. Discussion 6.1. Biology 6.2. Habitat use and population density SECOND PART: DISTRIBUTION AND HABITATS THROUGHOUT THE RANGE 7. Materials and methods 7.1. Data collection 7.2. Visit to others sites 8. Results 8.1. Data compilation 8.2. Visited places 8.2.1. Corozalito (south of Shipstern lagoon) 8.2.2. -
Thrinax Radiata Family: Arecaceae Florida Thatch Palm, Jamaican Thatch, Thatch Palm, Chit
Stephen H. Brown, Horticulture Agent Donna Cressman, Master Gardener Lee County Extension, Fort Myers, Florida (239) 533-7513 [email protected] http://lee.ifas.ufl.edu/hort/GardenHome.shtml Thrinax radiata Family: Arecaceae Florida thatch palm, Jamaican thatch, thatch palm, chit Florida Thatch Palm Synonyms (Discarded names): Cocothrinax martii, C. radiate, Thrinax floridana, T. martii, T. multiflora; T. wendlandiana Origin: Extreme southern mainland coast of Florida, Florida Keys, Bahamas, western Cuba, Cayman Islands, Jamaica, Hispaniola, Puerto Rico, Yucatan Peninsula, Honduras, Nicaragua U.S.D.A. Zone: 10A-12B (28°F leaf damage) Growth Rate: Slow Typical Height: 20’ Habit: Solitary; canopy of 12-20 leaves Crownshaft: None Leaf: Palmate, induplicate, circular, slightly folded; divided about halfway into segments that are split at the tips; pointed hastula Leaf Size: 4-5’ wide; segments 2.5’ long, 2” wide Salt Tolerance: High Drought Tolerance: High Wind Tolerance: High Light Requirements: Moderate, high Soil: Widely adaptable Nutritional Requirements: Low Potential Insect Pests: Aphids; scales Propagation: Seeds Human hazards: None Uses: Small gardens; containers; outdoors patios; roadways; parking lots; seasides; specimen Left: The infructescence (fruited stems) hang in a circle around the trunk, sometimes extending beyond the leaf. Natural Geographic Distribution The Florida Thatch Palm, Thrinax radiata, is indigenous to the extreme southern mainland coast of Florida, the Florida Keys, Bahamas, western Cuba, The Cayman Islands, Jamaica, Hispaniola, Puerto Rico, Honduras, Nicaragua, and the eastern coast of the Yucatan Peninsula in Mexico and Belize. In na- ture, this palm almost always grows within the range of salt-laden winds near coastal areas. It grows naturally in sandy or calcareous soils. -
Native Trees of Mexico: Diversity, Distribution, Uses and Conservation
Native trees of Mexico: diversity, distribution, uses and conservation Oswaldo Tellez1,*, Efisio Mattana2,*, Mauricio Diazgranados2, Nicola Kühn2, Elena Castillo-Lorenzo2, Rafael Lira1, Leobardo Montes-Leyva1, Isela Rodriguez1, Cesar Mateo Flores Ortiz1, Michael Way2, Patricia Dávila1 and Tiziana Ulian2 1 Facultad de Estudios Superiores Iztacala, Av. De los Barrios 1, Los Reyes Iztacala Tlalnepantla, Universidad Nacional Autónoma de México, Estado de México, Mexico 2 Wellcome Trust Millennium Building, RH17 6TN, Royal Botanic Gardens, Kew, Ardingly, West Sussex, United Kingdom * These authors contributed equally to this work. ABSTRACT Background. Mexico is one of the most floristically rich countries in the world. Despite significant contributions made on the understanding of its unique flora, the knowledge on its diversity, geographic distribution and human uses, is still largely fragmented. Unfortunately, deforestation is heavily impacting this country and native tree species are under threat. The loss of trees has a direct impact on vital ecosystem services, affecting the natural capital of Mexico and people's livelihoods. Given the importance of trees in Mexico for many aspects of human well-being, it is critical to have a more complete understanding of their diversity, distribution, traditional uses and conservation status. We aimed to produce the most comprehensive database and catalogue on native trees of Mexico by filling those gaps, to support their in situ and ex situ conservation, promote their sustainable use, and inform reforestation and livelihoods programmes. Methods. A database with all the tree species reported for Mexico was prepared by compiling information from herbaria and reviewing the available floras. Species names were reconciled and various specialised sources were used to extract additional species information, i.e. -
A New Subspecies of Anolis Porcatus (Sauna: Polychrotidae) from Western Cuba
Rev. Biol. Trop., 44(3)/45(1): 295-299, 1996-1997 A new subspecies of Anolis porcatus (Sauna: Polychrotidae) from Western Cuba O. Pérez-Beato 6780 W 2nd Ct. Apt. 212, Hialeah, Florida 33012, U.S.A. (Rec. l-IX-1995. Rev. ll-IX-1995. Acep. 22-11-1996) Abstract: A new subspecies of Anolis porcatus Gray, is described fromwestem Cuba. The main characters differenti ating Anolis porcattis aracelyae are a Iight blúe tint dorsum and an elongated ear opening. The distribution of the new taxon may be explained on the basis of allopatry in the Guaniguanico mountain range. Key words: Anolis porcatus, Cuba, Polychrotidae , subspecies Since the original description of Anolis por examined 325 additional specimens from popu catus (Gray 1840), this species was twice con lations throughout Cuba; unfortunately, sorne sidered a subspecies of Anolis carolinensis of tbis have been lost. Duméril and Bibron (Barbour 1937, Oliver The presence of a peculiar phenotype with a 1948), although Gray's allocation generally has light blue color in adult males and with an prevailed. The most complete systematic treat elongated ear opening in both sexes became ment was by Ruibal and Williams (1961). They evident in samples from western Cuba. This described the variability observed among and variation in ear shape had been noted by Ruibal between populations of A. porcatus across and Williams (1961) for Pinar de Río popula Cuba and proposed not fewer than four tions. The distribution of this phenotype hypotheses to explain the possible existence of ineludes almost the entire province of Pinar del several species and subspecies. -
Cfreptiles & Amphibians
HTTPS://JOURNALS.KU.EDU/REPTILESANDAMPHIBIANSTABLE OF CONTENTS IRCF REPTILES & AMPHIBIANSREPTILES • VOL15, & N AMPHIBIANSO 4 • DEC 2008 •189 28(1):44–46 • APR 2021 IRCF REPTILES & AMPHIBIANS CONSERVATION AND NATURAL HISTORY TABLE OF CONTENTS CubanFEATURE ARTICLES Green Anoles (Anolis porcatus): . Chasing Bullsnakes (Pituophis catenifer sayi) in Wisconsin: CommunalOn the Road to Understanding the Ecology Nestingand Conservation of the Midwest’s in Giant SerpentBromeliads ...................... Joshua M. Kapfer 190 . The Shared History of Treeboas (Corallus grenadensis) and Humans on Grenada: A Hypothetical Excursion ............................................................................................................................Robert W. Henderson 198 L. Yusnaviel García-Padrón RESEARCH ARTICLES Sociedad Espeleológica de Cuba, La Habana, Cuba; Sociedad Cubana de Zoología, La Habana 12000, Cuba ([email protected]) . The Texas Horned Lizard in Central and Western TexasPhotographs ....................... by the Emily author. Henry, Jason Brewer, Krista Mougey, and Gad Perry 204 . The Knight Anole (Anolis equestris) in Florida .............................................Brian J. Camposano, Kenneth L. Krysko, Kevin M. Enge, Ellen M. Donlan, and Michael Granatosky 212 CONSERVATION ALERT noles (Anolis spp.) lay single eggs buried in soil, under (22º32'20"N, 83º50'04"W; WGS 84; elev. 230 m asl). All of . World’s Mammals in Crisis ............................................................................................................................................................ -
The Development of Complex Tooth Shape in Reptiles
ORIGINAL RESEARCH ARTICLE published: 25 February 2014 doi: 10.3389/fphys.2014.00074 The development of complex tooth shape in reptiles Oldrich Zahradnicek 1,MarcelaBuchtova2,3, Hana Dosedelova 2,3 and Abigail S. Tucker 4* 1 Department of Teratology, Institute of Experimental Medicine, v.v.i., Academy of Sciences of the Czech Republic, Prague, Czech Republic 2 Laboratory of Animal Embryology, Institute of Animal Physiology and Genetics, v.v.i., Academy of Sciences of the Czech Republic, Brno, Czech Republic 3 Department of Anatomy, Histology and Embryology, Faculty of Veterinary Medicine, University of Veterinary and Pharmaceutical Sciences, Brno, Czech Republic 4 Department of Craniofacial Development and Stem Cell Biology, and Department of Orthodontics, King’s College London, Guy’s Hospital, London, UK Edited by: Reptiles have a diverse array of tooth shapes, from simple unicuspid to complex Cyril Charles, Ecole Normale multicuspid teeth, reflecting functional adaptation to a variety of diets and eating styles. Supérieure de Lyon, France In addition to cusps, often complex longitudinal labial and lingual enamel crests are Reviewed by: widespread and contribute to the final shape of reptile teeth. The simplest shaped Amel Gritli-Linde, University of Gothenburg, Sweden unicuspid teeth have been found in piscivorous or carnivorous ancestors of recent diapsid Daniel Graf, University of Zurich, reptiles and they are also present in some extant carnivores such as crocodiles and snakes. Switzerland However, the ancestral tooth shape for squamate reptiles is thought to be bicuspid, *Correspondence: indicating an insectivorous diet. The development of bicuspid teeth in lizards has recently Abigail S. Tucker, Department of been published, indicating that the mechanisms used to create cusps and crests are very Craniofacial Development and Stem Cell Biology, and Department of distinct from those that shape cusps in mammals. -
The Impact of Climate Change Measured at Relevant Spatial Scales: New Hope for Tropical Lizards
Global Change Biology (2013) 19, 3093–3102, doi: 10.1111/gcb.12253 The impact of climate change measured at relevant spatial scales: new hope for tropical lizards MICHAEL L. LOGAN*, RYAN K. HUYNH† ,RACHELA.PRECIOUS‡ and RYAN G. CALSBEEK* *Department of Biology, Dartmouth College, 78 College St., Hanover, NH 03755, USA, †Department of Ecology and Evolutionary Biology, Princeton University, 106 Guyot Hall, Princeton, NJ 08544, USA, ‡Department of Natural Resource Conservation, University of Massachusetts-Amherst, 160 Holdsworth Way, Amherst, MA 01003, USA Abstract Much attention has been given to recent predictions that widespread extinctions of tropical ectotherms, and tropical forest lizards in particular, will result from anthropogenic climate change. Most of these predictions, however, are based on environmental temperature data measured at a maximum resolution of 1 km2, whereas individuals of most species experience thermal variation on a much finer scale. To address this disconnect, we combined thermal perfor- mance curves for five populations of Anolis lizard from the Bay Islands of Honduras with high-resolution tempera- ture distributions generated from physical models. Previous research has suggested that open-habitat species are likely to invade forest habitat and drive forest species to extinction. We test this hypothesis, and compare the vulnera- bilities of closely related, but allopatric, forest species. Our data suggest that the open-habitat populations we studied will not invade forest habitat and may actually benefit from predicted warming for many decades. Conversely, one of the forest species we studied should experience reduced activity time as a result of warming, while two others are unlikely to experience a significant decline in performance. -
Xenosaurus Tzacualtipantecus. the Zacualtipán Knob-Scaled Lizard Is Endemic to the Sierra Madre Oriental of Eastern Mexico
Xenosaurus tzacualtipantecus. The Zacualtipán knob-scaled lizard is endemic to the Sierra Madre Oriental of eastern Mexico. This medium-large lizard (female holotype measures 188 mm in total length) is known only from the vicinity of the type locality in eastern Hidalgo, at an elevation of 1,900 m in pine-oak forest, and a nearby locality at 2,000 m in northern Veracruz (Woolrich- Piña and Smith 2012). Xenosaurus tzacualtipantecus is thought to belong to the northern clade of the genus, which also contains X. newmanorum and X. platyceps (Bhullar 2011). As with its congeners, X. tzacualtipantecus is an inhabitant of crevices in limestone rocks. This species consumes beetles and lepidopteran larvae and gives birth to living young. The habitat of this lizard in the vicinity of the type locality is being deforested, and people in nearby towns have created an open garbage dump in this area. We determined its EVS as 17, in the middle of the high vulnerability category (see text for explanation), and its status by the IUCN and SEMAR- NAT presently are undetermined. This newly described endemic species is one of nine known species in the monogeneric family Xenosauridae, which is endemic to northern Mesoamerica (Mexico from Tamaulipas to Chiapas and into the montane portions of Alta Verapaz, Guatemala). All but one of these nine species is endemic to Mexico. Photo by Christian Berriozabal-Islas. Amphib. Reptile Conserv. | http://redlist-ARC.org 01 June 2013 | Volume 7 | Number 1 | e61 Copyright: © 2013 Wilson et al. This is an open-access article distributed under the terms of the Creative Com- mons Attribution–NonCommercial–NoDerivs 3.0 Unported License, which permits unrestricted use for non-com- Amphibian & Reptile Conservation 7(1): 1–47.