Unisexual Ambystoma Ambystoma Laterale
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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? ............................................................................. -
Species of Greatest Conservation Need Species Accounts
2 0 1 5 – 2 0 2 5 Species of Greatest Conservation Need Species Accounts Appendix 1.4C-Amphibians Amphibian Species of Greatest Conservation Need Maps: Physiographic Provinces and HUC Watersheds Species Accounts (Click species name below or bookmark to navigate to species account) AMPHIBIANS Eastern Hellbender Northern Ravine Salamander Mountain Chorus Frog Mudpuppy Eastern Mud Salamander Upland Chorus Frog Jefferson Salamander Eastern Spadefoot New Jersey Chorus Frog Blue-spotted Salamander Fowler’s Toad Western Chorus Frog Marbled Salamander Northern Cricket Frog Northern Leopard Frog Green Salamander Cope’s Gray Treefrog Southern Leopard Frog The following Physiographic Province and HUC Watershed maps are presented here for reference with conservation actions identified in the species accounts. Species account authors identified appropriate Physiographic Provinces or HUC Watershed (Level 4, 6, 8, 10, or statewide) for specific conservation actions to address identified threats. HUC watersheds used in this document were developed from the Watershed Boundary Dataset, a joint project of the U.S. Dept. of Agriculture-Natural Resources Conservation Service, the U.S. Geological Survey, and the Environmental Protection Agency. Physiographic Provinces Central Lowlands Appalachian Plateaus New England Ridge and Valley Piedmont Atlantic Coastal Plain Appalachian Plateaus Central Lowlands Piedmont Atlantic Coastal Plain New England Ridge and Valley 675| Appendix 1.4 Amphibians Lake Erie Pennsylvania HUC4 and HUC6 Watersheds Eastern Lake Erie -
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. -
AMPHIBIANS of OHIO F I E L D G U I D E DIVISION of WILDLIFE INTRODUCTION
AMPHIBIANS OF OHIO f i e l d g u i d e DIVISION OF WILDLIFE INTRODUCTION Amphibians are typically shy, secre- Unlike reptiles, their skin is not scaly. Amphibian eggs must remain moist if tive animals. While a few amphibians Nor do they have claws on their toes. they are to hatch. The eggs do not have are relatively large, most are small, deli- Most amphibians prefer to come out at shells but rather are covered with a jelly- cately attractive, and brightly colored. night. like substance. Amphibians lay eggs sin- That some of these more vulnerable spe- gly, in masses, or in strings in the water The young undergo what is known cies survive at all is cause for wonder. or in some other moist place. as metamorphosis. They pass through Nearly 200 million years ago, amphib- a larval, usually aquatic, stage before As with all Ohio wildlife, the only ians were the first creatures to emerge drastically changing form and becoming real threat to their continued existence from the seas to begin life on land. The adults. is habitat degradation and destruction. term amphibian comes from the Greek Only by conserving suitable habitat to- Ohio is fortunate in having many spe- amphi, which means dual, and bios, day will we enable future generations to cies of amphibians. Although generally meaning life. While it is true that many study and enjoy Ohio’s amphibians. inconspicuous most of the year, during amphibians live a double life — spend- the breeding season, especially follow- ing part of their lives in water and the ing a warm, early spring rain, amphib- rest on land — some never go into the ians appear in great numbers seemingly water and others never leave it. -
Forestry Habitat Management Guidelines for Vernal Pool Wildlife
$8.00 Forestry Habitat Management Guidelines for Vernal Pool Wildlife Metropolitan Conservation Alliance a program of MCA Technical Paper Series: No. 6 Aram J. K. Calhoun, Ph.D. Department of Plant, Soil, and Environmental Sciences University of Maine, Orono, Maine 04469 Maine Audubon 20 Gilsland Farm Rd., Falmouth, Maine 04105 Phillip deMaynadier, Ph.D. Maine Department of Inland Fisheries and Wildlife Endangered Species Group, 650 State Street, Bangor, Maine 04401 A cooperative publication of the University of Maine, Maine Audubon, Maine Department of Inland Fisheries and Wildlife, Maine Department of Conservation, and the Wildlife Conservation Society. Cover illustration: Nancy J. Haver Suggested citation: Calhoun, A. J. K. and P. deMaynadier. 2004. Forestry habitat management guidelines for vernal pool wildlife. MCA Technical Paper No. 6, Metropolitan Conservation Alliance, Wildlife Conservation Society, Bronx, New York. Additional copies of this document can be obtained from: Maine Audubon 20 Gilsland Farm Road, Falmouth, ME 04105 (207) 781-2330 -------- Maine Department of Inland Fisheries and Wildlife 284 State Street, 41 SHS, Augusta, ME 04333 (207) 287-8000 -------- Metropolitan Conservation Alliance, Wildlife Conservation Society 68 Purchase Street, 3rd Floor, Rye, New York 10580 (914) 925-9175 ISBN 0-9724810-1-X ISSN 1542-8133 Printed on partially recycled paper. ACKNOWLEDGEMENTS THE PROCESS OF GUIDELINE DEVELOPMENT BENEFITED from active participation by Maine’s forest products industry (Georgia-Pacific Corp., Great Northern -
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. -
The Salamanders of Tennessee
Salamanders of Tennessee: modified from Lisa Powers tnwildlife.org Follow links to Nongame The Salamanders of Tennessee Photo by John White Salamanders are the group of tailed, vertebrate animals that along with frogs and caecilians make up the class Amphibia. Salamanders are ectothermic (cold-blooded), have smooth glandular skin, lack claws and must have a moist environment in which to live. 1 Amphibian Declines Worldwide, over 200 amphibian species have experienced recent population declines. Scientists have reports of 32 species First discovered in 1967, the golden extinctions, toad, Bufo periglenes, was last seen mainly species of in 1987. frogs. Much attention has been given to the Anurans (frogs) in recent years, however salamander populations have been poorly monitored. Photo by Henk Wallays Fire Salamander - Salamandra salamandra terrestris 2 Why The Concern For Salamanders in Tennessee? Their key role and high densities in many forests The stability in their counts and populations Their vulnerability to air and water pollution Their sensitivity as a measure of change The threatened and endangered status of several species Their inherent beauty and appeal as a creature to study and conserve. *Possible Factors Influencing Declines Around the World Climate Change Habitat Modification Habitat Fragmentation Introduced Species UV-B Radiation Chemical Contaminants Disease Trade in Amphibians as Pets *Often declines are caused by a combination of factors and do not have a single cause. Major Causes for Declines in Tennessee Habitat Modification -The destruction of natural habitats is undoubtedly the biggest threat facing amphibians in Tennessee. Housing, shopping center, industrial and highway construction are all increasing throughout the state and consequently decreasing the amount of available habitat for amphibians. -
Species Assessment for Jefferson Salamander
Species Status Assessment Class: Amphibia Family: Ambystomidae Scientific Name: Ambystoma jeffersonianum Common Name: Jefferson salamander Species synopsis: The distribution of the Jefferson salamander is restricted to the northeastern quarter of the United States extending as far to the southwest as Illinois and Kentucky; the species is represented in Canada only in a small area of southern Ontario. The habitat includes upland deciduous or mixed woodlands as well as bottomland forests adjacent to disturbed and agricultural lands. Breeding occurs in temporary ponds or semi-permanent wetlands (Gibbs et al. 2007). Hybridization occurs between the Jefferson salamander and the blue-spotted salamander (A. laterale). 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. 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 ____G4____________________________________________________________ ii. New York ____S4_____________________ Tracked by NYNHP? ___No____ Other Rank: Species of Northeast Regional Conservation Concern (Therres 1999) Species of Severe Concern and High Responsibility (NEPARC 2010) 1 Status Discussion: Jefferson salamander is considered to be locally abundant in suitable habitat across New York. It has been designated as a Species of Regional Conservation in the Northeast due to its unknown population status and taxonomic uncertainty (Therres 1999).