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Wood Frog (Rana Sylvatica): a Technical Conservation Assessment
Wood Frog (Rana sylvatica): A Technical Conservation Assessment Prepared for the USDA Forest Service, Rocky Mountain Region, Species Conservation Project March 24, 2005 Erin Muths1, Suzanne Rittmann1, Jason Irwin2, Doug Keinath3, Rick Scherer4 1 U.S. Geological Survey, Fort Collins Science Center, 2150 Centre Ave. Bldg C, Fort Collins, CO 80526 2 Department of Biology, Bucknell University, Lewisburg, PA 17837 3 Wyoming Natural Diversity Database, University of Wyoming, P.O. Box 3381, Laramie, WY 82072 4 Colorado State University, GDPE, Fort Collins, CO 80524 Peer Review Administered by Society for Conservation Biology Muths, E., S. Rittman, J. Irwin, D. Keinath, and R. Scherer. (2005, March 24). Wood Frog (Rana sylvatica): a technical conservation assessment. [Online]. USDA Forest Service, Rocky Mountain Region. Available: http://www.fs.fed.us/r2/projects/scp/assessments/woodfrog.pdf [date of access]. ACKNOWLEDGMENTS The authors would like to acknowledge the help of the many people who contributed time and answered questions during our review of the literature. AUTHORS’ BIOGRAPHIES Dr. Erin Muths is a Zoologist with the U.S. Geological Survey – Fort Collins Science Center. She has been studying amphibians in Colorado and the Rocky Mountain Region for the last 10 years. Her research focuses on demographics of boreal toads, wood frogs and chorus frogs and methods research. She is a principle investigator for the USDOI Amphibian Research and Monitoring Initiative and is an Associate Editor for the Northwestern Naturalist. Dr. Muths earned a B.S. in Wildlife Ecology from the University of Wisconsin, Madison (1986); a M.S. in Biology (Systematics and Ecology) from Kansas State University (1990) and a Ph.D. -
This Article Appeared in a Journal Published by Elsevier. the Attached
(This is a sample cover image for this issue. The actual cover is not yet available at this time.) This article appeared in a journal published by Elsevier. The attached copy is furnished to the author for internal non-commercial research and education use, including for instruction at the authors institution and sharing with colleagues. Other uses, including reproduction and distribution, or selling or licensing copies, or posting to personal, institutional or third party websites are prohibited. In most cases authors are permitted to post their version of the article (e.g. in Word or Tex form) to their personal website or institutional repository. Authors requiring further information regarding Elsevier’s archiving and manuscript policies are encouraged to visit: http://www.elsevier.com/copyright Author's personal copy Toxicon 60 (2012) 967–981 Contents lists available at SciVerse ScienceDirect Toxicon journal homepage: www.elsevier.com/locate/toxicon Antimicrobial peptides and alytesin are co-secreted from the venom of the Midwife toad, Alytes maurus (Alytidae, Anura): Implications for the evolution of frog skin defensive secretions Enrico König a,*, Mei Zhou b, Lei Wang b, Tianbao Chen b, Olaf R.P. Bininda-Emonds a, Chris Shaw b a AG Systematik und Evolutionsbiologie, IBU – Fakultät V, Carl von Ossietzky Universität Oldenburg, Carl von Ossietzky Strasse 9-11, 26129 Oldenburg, Germany b Natural Drug Discovery Group, School of Pharmacy, Medical Biology Center, Queen’s University, 97 Lisburn Road, Belfast BT9 7BL, Northern Ireland, UK article info abstract Article history: The skin secretions of frogs and toads (Anura) have long been a known source of a vast Received 23 March 2012 abundance of bioactive substances. -
Riparian Management and the Tailed Frog in Northern Coastal Forests
Forest Ecology and Management 124 (1999) 35±43 Riparian management and the tailed frog in northern coastal forests Linda Dupuis*,1, Doug Steventon Centre for Applied Conservation Biology, Department of Forest Sciences, University of British Columbia, Vancouver, BC, Canada V6T 1Z4 Ministry of Forests, Prince Rupert Region, Bag 5000, Smithers, BC, Canada V0J 2N0 Received 28 July 1998; accepted 19 January 1999 Abstract Although the importance of aquatic environments and adjacent riparian habitats for ®sh have been recognized by forest managers, headwater creeks have received little attention. The tailed frog, Ascaphus truei, inhabits permanent headwaters, and several US studies suggest that its populations decline following clear-cut logging practices. In British Columbia, this species is considered to be at risk because little is known of its abundance, distribution patterns in the landscape, and habitat needs. We characterized nine logged, buffered and old-growth creeks in each of six watersheds (n 54). Tadpole densities were obtained by area-constrained searches. Despite large natural variation in population size, densities decreased with increasing levels of ®ne sediment (<64 mm diameter), rubble, detritus and wood, and increased with bank width. The parameters that were correlated with lower tadpole densities were found at higher levels in clear-cut creeks than in creeks of other stand types. Tadpole densities were signi®cantly lower in logged streams than in buffered and old-growth creeks; thus, forested buffers along streams appear to maintain natural channel conditions. To prevent direct physical damage and sedimentation of channel beds, we suggest that buffers be retained along permanent headwater creeks. Creeks that display characteristics favoring higher tadpole densities, such as those that have coarse, stable substrates, should have management priority over less favorable creeks. -
A.11 Western Spadefoot Toad (Spea Hammondii) A.11.1 Legal and Other Status the Western Spadefoot Toad Is a California Designated Species of Special Concern
Appendix A. Species Account Butte County Association of Governments Western Spadefoot Toad A.11 Western Spadefoot Toad (Spea hammondii) A.11.1 Legal and Other Status The western spadefoot toad is a California designated Species of Special Concern. This species currently does not have any federal listing status. Although this species is not federally listed, it is addressed in the Recovery Plan for Vernal Pool Ecosystems of California and Southern Oregon (USFWS 2005). A.11.2 Species Distribution and Status A.11.2.1 Range and Status The western spadefoot toad historically ranged from Redding in Shasta County, California, to northwestern Baja California, Mexico (Stebbins 1985). This species was known to occur throughout the Central Valley and the Coast Ranges and along the coastal lowlands from San Francisco Bay to Mexico (Jennings and Hayes 1994). The western spadefoot toad has been extirpated throughout most southern California lowlands (Stebbins 1985) and from many historical locations within the Central Valley (Jennings and Hayes 1994, Fisher and Shaffer 1996). It has severely declined in the Sacramento Valley, and their density has been reduced in eastern San Joaquin Valley (Fisher and Shaffer 1996). While the species has declined in the Coast Range, they appear healthier and more resilient than those in the valleys. The population status and trends of the western spadefoot toad outside of California (i.e., Baja California, Mexico) are not well known. This species occurs mostly below 900 meters (3,000 feet) in elevation (Stebbins 1985). The average elevation of sites where the species still occurs is significantly higher than the average elevation for historical sites, suggesting that declines have been more pronounced in lowlands (USFWS 2005). -
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. -
Anura: Pelobatidae) MCZ by LIBRARY
Scientific Papers Natural History Museum The University of Kansas 18 July 2003 Number 30:1-13 Skeletal Development of Pelobates cultripes and a Comparison of the Osteogenesis of Pelobatid Frogs (Anura: Pelobatidae) MCZ By LIBRARY Z008 Anne M. Magl.a' JUL 2 3 Division of Hcrpetologi/, Natural History Museiiui and Biodiversity Researcli Center, and Department ojEonbgi^gMSpY Evolutionary Biology, The University of Kansas, Laivreuce, Kansas 66045, USA CONTENTS ABSTRACT 1 RESUMEN 2 INTRODUCTION 2 Acknowledgments 2 MATERIALS AND METHODS 2 RESULTS 3 Cranial Development 3 Hyobranchial Development 6 PosTCRANiAL Development 6 DISCUSSION 8 LITERATURE CITED 13 ABSTRACT The larval skeleton and osteogenesis of Pelobates cultripjes is described and compared to that of several pelobatoid and non-pelobatoid taxa. Several features of the larval skeleton are of inter- est, including: absence of a cartilaginous strip between the cornua trabeculae, type of articulation of cornua and suprarostrals, presence of adrostral tissues, and the condition of the otic process. By com- paring sequence of ossification events across taxa, several patterns of skeletal development for Pelobates cultripes emerge, including: conserved timing of prootic ossification, delayed onset of mentomeckelian ossification, and early formation of vomerine teeth. Several other developmental features, including the absence of a palatine (= neopalatine) bone and the formation of the frontoparietal, also are discussed. Key Words: Anura, Pelobatoidea, Pelobatidae, desarollo, osteologia, Pelobates, -
I Found a Frog…
I Found a Frog…What Do I Do With It? Finding a frog or toad in your backyard is a great discovery, especially if you live in an urban setting where these creatures are rarely found. Unless you have a large pond, most frogs and toads we find are transients taking up temporary residence where food and habitat seem good. But when autumn rolls around, starts to cool off, and the frog has not left, what do you do with your little friend? Here is some advice: Does this mean I have a new pet frog or toad? No! Please do not take in the animal. Not only is this illegal, but this is a wild animal that will not do well in a captive environment. Also, the proper artificial habitat is expensive, combined with the cost of food for the winter. And if you get attached to the animal (which is difficult not to do), it will be more difficult to release it in the spring. Many of the animal’s special survival skills will be lost in captivity over the winter. Frogs and toads hibernate in the winter, and rest their bodies for the following summer season. Frogs will want to slow down as daytime temperatures and lengths decrease, but it is not cool enough in our homes to lower metabolic rates. As a result, the frog remains active, will not eat, and will slowly starve. Some frogs with specialized care and live food will change their natural cycles and begin to feed, but if yours does not, it will die unnecessarily. -
Fish, Amphibians, and Reptiles)
6-3.1 Compare the characteristic structures of invertebrate animals... and vertebrate animals (fish, amphibians, and reptiles). Also covers: 6-1.1, 6-1.2, 6-1.5, 6-3.2, 6-3.3 Fish, Amphibians, and Reptiles sections Can I find one? If you want to find a frog or salamander— 1 Chordates and Vertebrates two types of amphibians—visit a nearby Lab Endotherms and Exotherms pond or stream. By studying fish, amphib- 2 Fish ians, and reptiles, scientists can learn about a 3 Amphibians variety of vertebrate characteristics, includ- 4 Reptiles ing how these animals reproduce, develop, Lab Water Temperature and the and are classified. Respiration Rate of Fish Science Journal List two unique characteristics for Virtual Lab How are fish adapted each animal group you will be studying. to their environment? 220 Robert Lubeck/Animals Animals Start-Up Activities Fish, Amphibians, and Reptiles Make the following Foldable to help you organize Snake Hearing information about the animals you will be studying. How much do you know about reptiles? For example, do snakes have eyelids? Why do STEP 1 Fold one piece of paper lengthwise snakes flick their tongues in and out? How into thirds. can some snakes swallow animals that are larger than their own heads? Snakes don’t have ears, so how do they hear? In this lab, you will discover the answer to one of these questions. STEP 2 Fold the paper widthwise into fourths. 1. Hold a tuning fork by the stem and tap it on a hard piece of rubber, such as the sole of a shoe. -
A Study of the Genus Scaphiopus: the Spade-Foot Toads
Great Basin Naturalist Volume 1 Number 1 Article 4 7-25-1939 A study of the genus Scaphiopus: the spade-foot toads Vasco M. Tanner Brigham Young University, Provo, UT Follow this and additional works at: https://scholarsarchive.byu.edu/gbn Recommended Citation Tanner, Vasco M. (1939) "A study of the genus Scaphiopus: the spade-foot toads," Great Basin Naturalist: Vol. 1 : No. 1 , Article 4. Available at: https://scholarsarchive.byu.edu/gbn/vol1/iss1/4 This Article is brought to you for free and open access by the Western North American Naturalist Publications at BYU ScholarsArchive. It has been accepted for inclusion in Great Basin Naturalist by an authorized editor of BYU ScholarsArchive. For more information, please contact [email protected], [email protected]. A STUI)^' ( )F THE CiI':NUS SCAIMIIOPUS^^) Thk Spade-foot Toads AWSCO M. TANNER Professor of Zoology and Entomolog\- Brigham Young University INTRODUCTION It is a little more than a Inindred years since Holbrook, 1836, erected the t;enus Scaplilopits descril)in,ij solifariiis, a species found along the Atlantic Coast, as the type of the genus. This species, how- ever, was described the year prevousl}-, 1835, by Harlan as Rana Jiolhrookii : thus holhrookii becomes the accepted name of the genotype. Many species and sub-species have been named since this time, the great majority of them, however, have been considered as synonyms. In this study I liave recognized the following species: holhrookii, hitrtcrii, couchii, homhifrons, haminondii, and interttiontamis. A vari- ety of holhrookii, described by Garman as alhiis, from Key West. Florida, may be a vaUd form ; but since I have had only a specimen or two for study. -
Frogs and Toads Defined
by Christopher A. Urban Chief, Natural Diversity Section Frogs and toads defined Frogs and toads are in the class Two of Pennsylvania’s most common toad and “Amphibia.” Amphibians have frog species are the eastern American toad backbones like mammals, but unlike mammals they cannot internally (Bufo americanus americanus) and the pickerel regulate their body temperature and frog (Rana palustris). These two species exemplify are therefore called “cold-blooded” (ectothermic) animals. This means the physical, behavioral, that the animal has to move ecological and habitat to warm or cool places to change its body tempera- similarities and ture to the appropriate differences in the comfort level. Another major difference frogs and toads of between amphibians and Pennsylvania. other animals is that amphibians can breathe through the skin on photo-Andrew L. Shiels L. photo-Andrew www.fish.state.pa.us Pennsylvania Angler & Boater • March-April 2005 15 land and absorb oxygen through the weeks in some species to 60 days in (plant-eating) beginning, they have skin while underwater. Unlike reptiles, others. Frogs can become fully now developed into insectivores amphibians lack claws and nails on their developed in 60 days, but many (insect-eaters). Then they leave the toes and fingers, and they have moist, species like the green frog and bullfrog water in search of food such as small permeable and glandular skin. Their can “overwinter” as tadpoles in the insects, spiders and other inverte- skin lacks scales or feathers. bottom of ponds and take up to two brates. Frogs and toads belong to the years to transform fully into adult Where they go in search of this amphibian order Anura. -
Recovery Strategy for the Great Basin Spadefoot (Spea Intermontana) in Canada
Species at Risk Act Recovery Strategy Series Adopted under Section 44 of SARA Recovery Strategy for the Great Basin Spadefoot (Spea intermontana) in Canada Great Basin Spadefoot 2017 1 Recommended citation: Environment and Climate Change Canada. 2017. Recovery Strategy for the Great Basin Spadefoot (Spea intermontana) in Canada. Species at Risk Act Recovery Strategy Series. Environment and Climate Change Canada, Ottawa. 2 parts, 31 pp. + 40 pp. For copies of the recovery strategy, or for additional information on species at risk, including the Committee on the Status of Endangered Wildlife in Canada (COSEWIC) Status Reports, residence descriptions, action plans, and other related recovery documents, please visit the Species at Risk (SAR) Public Registry1. Cover illustration: © Karl Larsen Également disponible en français sous le titre « Programme de rétablissement du crapaud du Grand Bassin (Spea intermontana) au Canada » © Her Majesty the Queen in Right of Canada, represented by the Minister of Environment and Climate Change, 2017. All rights reserved. ISBN 978-0-660-24364-1 Catalogue no. En3-4/279-2017E-PDF Content (excluding the illustrations) may be used without permission, with appropriate credit to the source. 1 http://sararegistry.gc.ca/default.asp?lang=En&n=24F7211B-1 RECOVERY STRATEGY FOR THE GREAT BASIN SPADEFOOT (Spea intermontana) IN CANADA 2017 Under the Accord for the Protection of Species at Risk (1996), the federal, provincial, and territorial governments agreed to work together on legislation, programs, and policies to protect wildlife species at risk throughout Canada. In the spirit of cooperation of the Accord, the Government of British Columbia has given permission to the Government of Canada to adopt the Recovery Plan for the Great Basin Spadefoot (Spea intermontana) in British Columbia (Part 2) under Section 44 of the Species at Risk Act (SARA). -
How Ecology and Evolution Shape Species Distributions and Ecological Interactions Across Time and Space
HOW ECOLOGY AND EVOLUTION SHAPE SPECIES DISTRIBUTIONS AND ECOLOGICAL INTERACTIONS ACROSS TIME AND SPACE by IULIAN GHERGHEL Submitted in partial fulfillment of the requirements for the degree of Doctor of Philosophy Advisor: Ryan A. Martin Department of Biology CASE WESTERN RESERVE UNIVERSITY January, 2021 CASE WESTERN RESERVE UNIVERSITY SCHOOL OF GRADUATE STUDIES We hereby approve the dissertation of Iulian Gherghel Candidate for the degree of Doctor of Philosophy* Committee Chair Dr. Ryan A. Martin Committee Member Dr. Sarah E. Diamond Committee Member Dr. Jean H. Burns Committee Member Dr. Darin A. Croft Committee Member Dr. Viorel D. Popescu Date of Defense November 17, 2020 * We also certify that written approval has been obtained for any proprietary material contained therein TABLE OF CONTENTS List of tables ........................................................................................................................ v List of figures ..................................................................................................................... vi Acknowledgements .......................................................................................................... viii Abstract ............................................................................................................................. iix INTRODUCTION............................................................................................................. 1 CHAPTER 1. POSTGLACIAL RECOLONIZATION OF NORTH AMERICA BY SPADEFOOT TOADS: INTEGRATING