Blue-Spotted Salamander Fact Sheet
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Western Tiger Salamander,Ambystoma Mavortium
COSEWIC Assessment and Status Report on the Western Tiger Salamander Ambystoma mavortium Southern Mountain population Prairie / Boreal population in Canada Southern Mountain population – ENDANGERED Prairie / Boreal population – SPECIAL CONCERN 2012 COSEWIC status reports are working documents used in assigning the status of wildlife species suspected of being at risk. This report may be cited as follows: COSEWIC. 2012. COSEWIC assessment and status report on the Western Tiger Salamander Ambystoma mavortium in Canada. Committee on the Status of Endangered Wildlife in Canada. Ottawa. xv + 63 pp. (www.registrelep-sararegistry.gc.ca/default_e.cfm). Previous report(s): COSEWIC. 2001. COSEWIC assessment and status report on the tiger salamander Ambystoma tigrinum in Canada. Committee on the Status of Endangered Wildlife in Canada. Ottawa. vi + 33 pp. (www.sararegistry.gc.ca/status/status_e.cfm). Schock, D.M. 2001. COSEWIC assessment and status report on the tiger salamander Ambystoma tigrinum in Canada, in COSEWIC assessment and status report on the tiger salamander Ambystoma tigrinum in Canada. Committee on the Status of Endangered Wildlife in Canada. Ottawa. 1-33 pp. Production note: COSEWIC would like to acknowledge Arthur Whiting for writing the status report on the Western Tiger Salamander, Ambystoma mavortium, in Canada, prepared under contract with Environment Canada. This report was overseen and edited by Kristiina Ovaska, Co-chair of the COSEWIC Amphibians and Reptiles Specialist Subcommittee. For additional copies contact: COSEWIC Secretariat c/o Canadian Wildlife Service Environment Canada Ottawa, ON K1A 0H3 Tel.: 819-953-3215 Fax: 819-994-3684 E-mail: COSEWIC/[email protected] http://www.cosewic.gc.ca Également disponible en français sous le titre Ếvaluation et Rapport de situation du COSEPAC sur la Salamandre tigrée de l’Ouest (Ambystoma mavortium) au Canada. -
Blue–Spotted Salamander Ambystoma Laterale Status: Wisconsin – Common Minnesota – Common Iowa – Endangered
Species Descriptions Blue–spotted Salamander Ambystoma laterale Status: Wisconsin – Common Minnesota – Common Iowa – Endangered 1 cm Size at hatching, 8 – 10 mm total length; at metamorphosis, ~ 34 mm snout–vent length The Blue-spotted Salamander is one of four mole salamanders in our region. Other mole salamanders include the Spotted, Small-mouthed, and Tiger Salamanders. As adults, mole salamanders live under cover objects such as rotting logs or in burrows in the forest floor (Parmelee 1993). In early spring (March and April), adults migrate to temporary ponds to breed. Larvae develop during spring and summer and usually metamorphose in the fall. The Blue-spotted Salamander is a woodland species of northern North America. The eggs are laid in small clumps (7–40 eggs) attached to vegetation or debris at the bottom of ponds. The larvae are similar to Spotted Salamanders but are more darkly colored with the fins mottled with black, and dark blotches on the dorsum. Blue-spotted Salamanders metamorphose at about the same size as Spotted Salamanders but are darker, sometimes with flecks of blue. 14 15 Spotted Salamander Ambystoma maculatum Status: Wisconsin – Locally abundant Minnesota – Status to be determined 1 cm Size at hatching, 12 – 17 mm; at metamorphosis, 49 – 60 mm total length The Spotted Salamander is present only in the northeastern part of our range (where it is sympatric with up to two other mole salamanders). Females deposit eggs in a firm oval mass (60–100 mm in diameter) attached to vegetation near the surface of the water. The eggs (1–250 per mass) are black, but the egg mass may be clear or milky, with a greenish hue because of symbiotic algae. -
Spotted Salamander (Ambystoma Maculafum)
Spotted Salamander (Ambystoma maculafum) RANGE: Nova Scotia and the Gaspe Peninsula to s. On- BREEDINGPERIOD: March to mid-April. Mass breeding tario, s. through Wisconsin, s. Illinois excluding prairie migrations occur in this species: individuals enter and regions, toe. Kansas andTexas, and through the Eastern leave breeding ponds using the same track each year, United States, except Florida, the Delmarva Peninsula, and exhibit fidelity to breeding ponds (Shoop 1956, and s. New Jersey. 1974). Individuals may not breed in consecutive years (Husting 1965). Breeding migrations occur during RELATIVE ABUNDANCEIN NEW ENGLAND:Common steady evening rainstorms. though populations declining, probably due to acid pre- cipitation. EGG DEPOSITION:1 to 6 days after first appearance of adults at ponds (Bishop 1941 : 114). HABITAT:Fossorial; found in moist woods, steambanks, beneath stones, logs, boards. Prefers deciduous or NO. EGGS/MASS:100 to 200 eggs, average of 125, laid in mixed woods on rocky hillsides and shallow woodland large masses of jelly, sometimes milky, attached to stems ponds or marshy pools that hold water through the sum- about 15 cm (6 inches) under water. Each female lays 1 to mer for breeding. Usually does not inhabit ponds con- 10 masses (average of 2 to 3) of eggs (Wright and Allen taining fish (Anderson 1967a). Terrestrial hibernator. In 1909).Woodward (1982)reported that females breeding summer often wanders far from water source. Found in in permanent ponds produced smaller, more numerous low oak-hickory forests with creeks and nearby swamps eggs than females using temporary ponds. in Illinois (Cagle 1942, cited in Smith 1961 :30). -
Heterotrophic Carbon Fixation in a Salamander-Alga Symbiosis
bioRxiv preprint doi: https://doi.org/10.1101/2020.02.14.948299; this version posted February 18, 2020. The copyright holder for this preprint (which was not certified by peer review) is the author/funder, who has granted bioRxiv a license to display the preprint in perpetuity. It is made available under aCC-BY 4.0 International license. Heterotrophic Carbon Fixation in a Salamander-Alga Symbiosis. John A. Burns1,2, Ryan Kerney3, Solange Duhamel1,4 1Lamont-Doherty Earth Observatory of Columbia University, Division of Biology and Paleo Environment, Palisades, NY 2Bigelow Laboratory for Ocean Sciences, East Boothbay, ME 3Gettysburg College, Biology, Gettysburg, PA 4University of Arizona, Department of Molecular and Cellular Biology, Tucson, AZ Abstract The unique symbiosis between a vertebrate salamander, Ambystoma maculatum, and unicellular green alga, Oophila amblystomatis, involves multiple modes of interaction. These include an ectosymbiotic interaction where the alga colonizes the egg capsule, and an intracellular interaction where the alga enters tissues and cells of the salamander. One common interaction in mutualist photosymbioses is the transfer of photosynthate from the algal symbiont to the host animal. In the A. maculatum-O. amblystomatis interaction, there is conflicting evidence regarding whether the algae in the egg capsule transfer chemical energy captured during photosynthesis to the developing salamander embryo. In experiments where we took care to separate the carbon fixation contributions of the salamander embryo and algal symbionts, we show that inorganic carbon fixed by A. maculatum embryos reaches 2% of the inorganic carbon fixed by O. amblystomatis algae within an egg capsule after 2 hours in the light. -
The Origins of Chordate Larvae Donald I Williamson* Marine Biology, University of Liverpool, Liverpool L69 7ZB, United Kingdom
lopmen ve ta e l B Williamson, Cell Dev Biol 2012, 1:1 D io & l l o l g DOI: 10.4172/2168-9296.1000101 e y C Cell & Developmental Biology ISSN: 2168-9296 Research Article Open Access The Origins of Chordate Larvae Donald I Williamson* Marine Biology, University of Liverpool, Liverpool L69 7ZB, United Kingdom Abstract The larval transfer hypothesis states that larvae originated as adults in other taxa and their genomes were transferred by hybridization. It contests the view that larvae and corresponding adults evolved from common ancestors. The present paper reviews the life histories of chordates, and it interprets them in terms of the larval transfer hypothesis. It is the first paper to apply the hypothesis to craniates. I claim that the larvae of tunicates were acquired from adult larvaceans, the larvae of lampreys from adult cephalochordates, the larvae of lungfishes from adult craniate tadpoles, and the larvae of ray-finned fishes from other ray-finned fishes in different families. The occurrence of larvae in some fishes and their absence in others is correlated with reproductive behavior. Adult amphibians evolved from adult fishes, but larval amphibians did not evolve from either adult or larval fishes. I submit that [1] early amphibians had no larvae and that several families of urodeles and one subfamily of anurans have retained direct development, [2] the tadpole larvae of anurans and urodeles were acquired separately from different Mesozoic adult tadpoles, and [3] the post-tadpole larvae of salamanders were acquired from adults of other urodeles. Reptiles, birds and mammals probably evolved from amphibians that never acquired larvae. -
Amphibiaweb's Illustrated Amphibians of the Earth
AmphibiaWeb's Illustrated Amphibians of the Earth Created and Illustrated by the 2020-2021 AmphibiaWeb URAP Team: Alice Drozd, Arjun Mehta, Ash Reining, Kira Wiesinger, and Ann T. Chang This introduction to amphibians was written by University of California, Berkeley AmphibiaWeb Undergraduate Research Apprentices for people who love amphibians. Thank you to the many AmphibiaWeb apprentices over the last 21 years for their efforts. Edited by members of the AmphibiaWeb Steering Committee CC BY-NC-SA 2 Dedicated in loving memory of David B. Wake Founding Director of AmphibiaWeb (8 June 1936 - 29 April 2021) Dave Wake was a dedicated amphibian biologist who mentored and educated countless people. With the launch of AmphibiaWeb in 2000, Dave sought to bring the conservation science and basic fact-based biology of all amphibians to a single place where everyone could access the information freely. Until his last day, David remained a tirelessly dedicated scientist and ally of the amphibians of the world. 3 Table of Contents What are Amphibians? Their Characteristics ...................................................................................... 7 Orders of Amphibians.................................................................................... 7 Where are Amphibians? Where are Amphibians? ............................................................................... 9 What are Bioregions? ..................................................................................10 Conservation of Amphibians Why Save Amphibians? ............................................................................. -
Massachusetts Animals – Spotted Salamander
Massachusetts Animals – Spotted Salamander Facts at a Glance TYPE OF ANIMAL Amphibian SCIENTIFIC NAME Ambystoma maculatum FOUND WHERE Eastern United States from Maine to South Carolina HEIGHT/LENGTH 6 – 10 in. long (15 – 25 cm) WEIGHT Average about 120 – 200 g, Females often bigger than males CONSERVATION STATUS Least Concern Easily characterized by their deep brown or black skin dotted with trademark yellow and orange toned spots along the back and sides. As amphibians, they have smooth and glossy skin, not scales, and live in damp areas close to ponds and vernal pools. Their appearance varies through their life cycles, starting at a dull greenish color with external, frilly gills as a hatchling and eventually growing into their classic spots. Despite the fact that these salamanders are quite widespread, they are often elusive and hard to find. They like to hide underground or beneath rocks, logs, and fallen root systems. HABITAT LIFE & BEHAVIOUR Spotted Salamanders are commonly found Spotted salamanders start their lives in water as small across Massachusetts and all along the eastern nymphs with external gills. Mothers lay their eggs in coast of the United States, even into parts of early spring, often at the same time and location year eastern Canada. They live in forested areas, after year. After a few weeks, more than 200 eggs will typically found close to water sources like hatch and grow into juveniles. Juvenile salamanders ponds, wetlands, and seasonal, vernal pools. live in water until they grow into adult size, then move They enjoy damp and hidden environments. onto land, where they can live for about 20 years. -
Successful Reproduction of the Mole Salamander Ambystoma Talpoideum in Captivity, with an Emphasis on Stimuli Environmental Determinants
SHORT NOTE The Herpetological Bulletin 141, 2017: 28-31 Successful reproduction of the mole salamander Ambystoma talpoideum in captivity, with an emphasis on stimuli environmental determinants AXEL HERNANDEZ Department of Environmental Sciences, Faculty of Sciences and Technics, University Pasquale Paoli of Corsica, Corte, 20250, France Author Email: [email protected] ABSTRACT - Generating and promoting evidence-based husbandry protocols for urodeles, commonly known as newts and salamanders, is urgently needed because most of the up-to-date ex situ programs are focused on frogs and toads than Urodela. Data on biology, life history, ecology and environmental parameters are lacking for many species and are needed to establish suitable husbandry and breeding conditions in captive environments. Two adult females and two adult males, of the mole salamander Ambystoma talpoideum successfully reproduced in captivity. It was found that reproduction of this species depends on various complex stimuli: including natural photoperiod 12:12, rainwater (acidic to neutral pH) and an aquarium full of various debris. Additionally high temperature variations ranging from 2 °C to 17 °C (a decrease followed by an increase) between November and February showed that it is possible to breed adults in aquariums provided the right stimuli are applied at the right moment of time in winter. A. talpoideum shows an explosive breeding mode as previously reported for the whole genus Ambystoma. INTRODUCTION with an emphasis on the environmental determinant stimuli involved. These data may assist in improving breeding these ince the 1980s, the current global amphibian extinction salamanders under artificial conditions. crisis has been discussed and acknowledged (Wake, A. -
EARTH Ltd PME Threatened Habitats Handout
501-C-3 at Southwick’s Zoo, 2 Southwick Street, Mendon, MA 01756 PROTECTING MY EARTH: LOCALLY THREATENED HABITATS (MA) FACTS & FIGURES “Protecting My EARTH” is an environmental education program offered by EARTH Ltd. to help students learn how to take better care of their community and their planet. KEY TERMS AND DEFINITIONS • Conservation: a careful preservation and protection of something; especially planned management of a natural resource to prevent exploitation, destruction, or neglect • Habitat: the place or environment where a plant or animal naturally or normally lives and grows • Ecosystem: everything that exists in a particular environment • Endangered: a species in danger of becoming extinct • Extinct: no longer existing • Threatened: having an uncertain chance of continued survival; likely to become an endangered species • Vulnerable: easily damaged; likely to become an endangered species • CITES - Convention on International Trade of Endangered Species of Wild Fauna and Flora: an international agreement between governments effective since 1975. Its aim is to ensure that international trade in specimens of wild animals and plants does not threaten their survival. Roughly 5,600 species of animals and 30,000 species of plants are protected by CITES as of 2013. There are currently 181 countries (of about 196) that are contracting parties. • IUCN - International Union for the Conservation of Nature: world’s oldest and largest global environmental organization, with almost 1,300 government and NGO Members and more than 15,000 volunteer experts in 185 countries. Their work focuses on valuing and conserving nature, ensuring effective and equitable governance of its use, and deploying nature-based solutions to global challenges in climate, food and development. -
Blue-Spotted Salamander
Species Status Assessment Class: Amphibia Family: Ambystomatidae Scientific Name: Ambystoma laterale Common Name: Blue-spotted salamander Species synopsis: The blue-spotted salamander has the northernmost distribution of any Ambystoma species, occurring in east-central North America as far north as Labrador, with its distribution dipping southward into the northeastern United States only as far as northern New Jersey. In New York, this salamander occurs in a patchy distribution outside of high elevation areas; its occurrence on Long Island is only in the farthest eastern reaches. Blue-spotted salamander habitat is the moist forest floor of deciduous or mixed woodlands near ephemeral bodies of water. Reliable population trends are not available for this salamander. Hybridization occurs between blue-spotted salamander and Jefferson salamander (A. jeffersonianum). Broadly referred to as the Jefferson complex, the variety of hybrids includes up to five different chromosomal combinations. Some of the hybrids have been called Tremblay’s salamander or silvery salamander, but most references are to “Jefferson complex.” This unusual situation has lead to difficulty in defining the distribution of blue-spotted salamander and Jefferson salamander, the hybrids of which are very difficult to distinguish, typically, without genetic testing in conjunction with their appearance. In Connecticut, the blue-spotted diploid and the blue-spotted complex have been listed individually, as Threatened and Special Concern respectively but no other state or province has made this distinction in listing status. 1 I. Status a. Current and Legal Protected Status i. Federal ___Not Listed_______________________ Candidate? ___No____ ii. New York ___Special Concern; SGCN_____________________________________ b. Natural Heritage Program Rank i. Global _____G5__________________________________________________________ ii. -
Abundance, Distribution, Population Structure, and Substrate Use of Ambystoma Altamirani Along the Arroyo Los Axolotes, State of Mexico, Mexico
Herpetological Conservation and Biology 15(1):188–197. Submitted: 16 August 2019; Accepted: 23 February 2020; Published: 30 April 2020. ABUNDANCE, DISTRIBUTION, POPULATION STRUCTURE, AND SUBSTRATE USE OF AMBYSTOMA ALTAMIRANI ALONG THE ARROYO LOS AXOLOTES, STATE OF MEXICO, MEXICO VIRIDIANA VILLARREAL HERNÁNDEZ1, GEOFFREY R. SMITH2, RAYMUNDO MONTOYA AYALA3, AND JULIO A. LEMOS-ESPINAL1,4 1Laboratorio de Ecología - Unidad de Biotecnología y Prototipos, Facultad de Estudios Superiores Iztacala, Avendina Los Barrios 1, Los Reyes Iztacala, Tlalnepantla, Estado de México, 54090, México 2Department of Biology, Denison University, Granville, Ohio 43023, USA 3Laboratorio de Cómputo - Unidad de Biotecnología y Prototipos, Facultad de Estudios Superiores Iztacala, Avenida Los Barrios 1, Los Reyes Iztacala, Tlalnepantla, Estado de México, 54090, México 4Corresponding author: e-mail: [email protected] Abstract.—Ambystomatid salamanders in central Mexico are confronted by anthropogenic threats that can limit their distribution and abundance. Ambystoma altamirani (Mountain Stream Siredon) is listed as Endangered by the International Union for Conservation of Nature (IUCN) Red List and as Threatened by the Mexican government. We report on the distribution, abundance, occupancy, population structure, and substrate use of A. altamirani, a stream dwelling salamander, along the Arroyo los Axolotes, Sierra de las Cruces, Mexico. We observed A. altamirani at least once during repeated surveys between February 2018 to December 2018 in 24 of 25 permanent 5-m long reaches separated by 40 m. The best model for occupancy had constant occupancy, detection, extinction, and colonization probabilities. Sites that dried at some time during the study had fewer observed individuals than those that did not dry. Size structure was relatively constant throughout the year, except for the appearance of small larvae in May, June, and July. -
AMPHIBIA: CAUDATA: AMBYSTOMATIDAE Catalogue Of
75.1 AMPHIBIA: CAUDATA: AMBYSTOMATIDAE AMBYSTOMA Catalogue of American Amphibians and Reptiles. Acholotes: Cope, 1867:184. An incorrect subsequent spelling ofAxolotes Owen, 1844; without nomenclatural status. TIHEN,JOSEPHA. 1969. Ambystoma. Pectoglossa Mivart, 1867:698. Type-species Plethodon persimi· lis Gray, 1859 (= Salamandra jeffersoniana Green, 1827), by monotypy. A.mbystoma Salamandroides: Boulenger, 1882:38. An incorrect subsequent Mole salamanders spelling of Salamandroidis Fitzinger, 1843; without no· menclatural status. Axolotus Jarocki, 1822:179. Type-species Siren pisciformis Linguaelapsus Cope, 1887:88. Type-species Amblystoma annu• Shaw, 1802 (= Gyrinus mexicanus Shaw, 1789), by sub• latum Cope, 1886, by subsequent designation (Dunn and sequent designation (Smith and Tihen, 1961b). See No• Dunn, 1940). menclatural History. Plioambystoma Adams and Martin, 1929:17. Type-species Philhydrus Brookes, 1828:16. Type-species Siren pisciformis Plioambystoma kansense Adams and Martin, 1929, by Shaw, 1802 (= Gyrinus mexicanus Shaw, 1789), by mono• monotypy. typy. See Nomenclatural History. Bathysiredon Dunn, 1939:1. Type-species Siredon dumerilii Siredon Wagler, 1830:209, 210. Type-species Siredon axolotl Duges, 1870, by original designation. Wagler, 1830 (= Gyrinus mexicanus Shaw, 1789), by Lanebatrachus Taylor, 1941:180. Type-species Lanebatrachus monotypy. See Nomenclatural History. martini Taylor, 1941 (= Plioambystoma kansense Adams Phyllhydrus Gray, 1831:108. Type-species Siren pisciformis and Martin, 1929), by original designation. Shaw,1802 (= Gyrinus mexicanus Shaw, 1789), by mono• Ogallalabatrachus Taylor, 1941 :181. Type-species Ogallala• typy (although Gray suggested other species as possibly batrachus horarium Taylor, 1941 (= Plioambystoma kan• referable to this genus). See Nomenclatural History. sense Adams and Martin, 1929), by original designation. Axolot Bonaparte, 1831:77. Type-species Siren pisciformis Shaw, 1802 (= Gyrinus mexicanus Shaw, 1789), by im• • CONTENT.