Spotted Salamander (Ambystoma Maculafum)
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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. -
The Natural History, Distribution, and Phenotypic Variation of Cave-Dwelling Spring Salamanders, Gyrinophilus Spp
Marshall University Marshall Digital Scholar Theses, Dissertations and Capstones 2005 The aN tural History, Distribution, and Phenotypic Variation of Cave-dwelling Spring Salamanders, Gyrinophilus spp. Cope (Plethodontidae), in West Virginia Michael Steven Osbourn Follow this and additional works at: http://mds.marshall.edu/etd Part of the Aquaculture and Fisheries Commons, and the Ecology and Evolutionary Biology Commons Recommended Citation Osbourn, Michael Steven, "The aN tural History, Distribution, and Phenotypic Variation of Cave-dwelling Spring Salamanders, Gyrinophilus spp. Cope (Plethodontidae), in West Virginia" (2005). Theses, Dissertations and Capstones. Paper 735. This Thesis is brought to you for free and open access by Marshall Digital Scholar. It has been accepted for inclusion in Theses, Dissertations and Capstones by an authorized administrator of Marshall Digital Scholar. For more information, please contact [email protected]. The Natural History, Distribution, and Phenotypic Variation of Cave-dwelling Spring Salamanders, Gyrinophilus spp. Cope (Plethodontidae), in West Virginia. Thesis submitted to The Graduate College of Marshall University In partial fulfillment of the Requirements for the degree of Master of Science Biological Sciences By Michael Steven Osbourn Thomas K. Pauley, Committee Chairperson Daniel K. Evans, PhD Thomas G. Jones, PhD Marshall University May 2005 Abstract The Natural History, Distribution, and Phenotypic Variation of Cave-dwelling Spring Salamanders, Gyrinophilus spp. Cope (Plethodontidae), in West Virginia. Michael S. Osbourn There are over 4000 documented caves in West Virginia, potentially providing refuge and habitat for a diversity of amphibians and reptiles. Spring Salamanders, Gyrinophilus porphyriticus, are among the most frequently encountered amphibians in caves. Surveys of 25 caves provided expanded distribution records and insight into ecology and diet of G. -
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? ............................................................................. -
Subterranean Reproduction of the Southern Two-Lined Salamander (Eurycea Cirrigera) from Short Mountain, Tennessee
Herpetological Conservation and Biology 2(2):106-112. Submitted: 15 April 2007; Accepted: 7 July 2007 SUBTERRANEAN REPRODUCTION OF THE SOUTHERN TWO-LINED SALAMANDER (EURYCEA CIRRIGERA) FROM SHORT MOUNTAIN, TENNESSEE 1,2 1 MATTHEW L. NIEMILLER AND BRIAN T. MILLER 1Department of Biology, Middle Tennessee State University, Murfreesboro, Tennessee 37132, USA 2Corresponding author/Present Address: Department of Ecology and Evolutionary Biology, University of Tennessee, Knoxville, Tennessee 37996, USA, e-mail: [email protected] Abstract.—The Southern Two-lined Salamander, Eurycea cirrigera, typically inhabits the margins of small, rocky streams, springs, and seeps in forested areas. The species is found only occasionally in subterranean habitats and, consequently, is considered a cave visitor (accidental or trogloxene). However, we discovered egg clutches in the deep cave zone of a subterranean stream during January and February 2005, indicating that some individuals are adapted to reproduce in caves. Eggs were attached singly to form monolayer masses on the undersurfaces of submerged rocks; females were found attending three of nine clutches. We determined the total number of eggs/clutch, mass surface area, egg and embryo size, and stage of development using digital images of each clutch. Embryo length correlated positively with developmental stage. Duration of embryonic period ranged from 35-42 days; consequently, eggs were laid from early to mid-January and larvae hatched from late February to early March. Adult males and females migrated into the cave to breed during late autumn. Males exited the cave after mating; whereas, females brooded their eggs and exited the cave only after eggs hatched. Larvae drifted downstream and out of the cave following heavy winter and early spring rains. -
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. -
Northern Spring Salamander Fact Sheet
WILDLIFE IN CONNECTICUT STATE THREATENED SPECIES © COURTESY D. QUINN © COURTESY Northern Spring Salamander Gyrinophilus p. porphyriticus Background and Range The northern spring salamander is a brightly-colored member of the lungless salamander family (Plethodontidae). True to its name, it resides in cool water springs and streams, making it an excellent indicator of a clean, well- oxygenated water source. Due to its strict habitat and clean water requirements, it is only found in a handful of locations within Connecticut. The Central Connecticut Lowlands divide this amphibian's range into distinct populations. Litchfield and Hartford Counties support the greatest populations of spring salamanders. This salamander is listed as a threatened species in Connecticut. In North America, the spring salamander occurs from extreme southeastern Canada south through New England, west to Ohio, and south down the Appalachians as far as northern Georgia and Alabama. Description This large, robust salamander ranges in color from salmon to reddish-brown to purplish-brown, with a translucent white underbelly. The snout appears “square” when viewed from above and the salamander has well-defined grooves near its eyes to its snout. The tail is laterally flattened with a fin-like tip. Young spring salamanders are lighter in color and have small gills. Their coloration does not have deeper reddish tints until adulthood. Total length ranges from 5 to 7.5 inches. Habitat and Diet Spring salamanders require very clean, cool, and well-oxygenated water. They can be found in streams, brooks, and seepage areas. Preferred habitat lies within steep, rocky hemlock forests. This species is intolerant to disturbances. -
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. -
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. -
The Symbiotic Green Algae, Oophila (Chlamydomonadales
University of Connecticut OpenCommons@UConn Master's Theses University of Connecticut Graduate School 12-16-2016 The yS mbiotic Green Algae, Oophila (Chlamydomonadales, Chlorophyceae): A Heterotrophic Growth Study and Taxonomic History Nikolaus Schultz University of Connecticut - Storrs, [email protected] Recommended Citation Schultz, Nikolaus, "The yS mbiotic Green Algae, Oophila (Chlamydomonadales, Chlorophyceae): A Heterotrophic Growth Study and Taxonomic History" (2016). Master's Theses. 1035. https://opencommons.uconn.edu/gs_theses/1035 This work is brought to you for free and open access by the University of Connecticut Graduate School at OpenCommons@UConn. It has been accepted for inclusion in Master's Theses by an authorized administrator of OpenCommons@UConn. For more information, please contact [email protected]. The Symbiotic Green Algae, Oophila (Chlamydomonadales, Chlorophyceae): A Heterotrophic Growth Study and Taxonomic History Nikolaus Eduard Schultz B.A., Trinity College, 2014 A Thesis Submitted in Partial Fulfillment of the Requirements for the Degree of Master of Science at the University of Connecticut 2016 Copyright by Nikolaus Eduard Schultz 2016 ii ACKNOWLEDGEMENTS This thesis was made possible through the guidance, teachings and support of numerous individuals in my life. First and foremost, Louise Lewis deserves recognition for her tremendous efforts in making this work possible. She has performed pioneering work on this algal system and is one of the preeminent phycologists of our time. She has spent hundreds of hours of her time mentoring and teaching me invaluable skills. For this and so much more, I am very appreciative and humbled to have worked with her. Thank you Louise! To my committee members, Kurt Schwenk and David Wagner, thank you for your mentorship and guidance.