Pulsed Flow Effects on the Foothill Yellow-Legged Frog (Rana Boylii): Integration of Empirical, Experimental and Hydrodynamic Modeling
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Character Assessment, Genus Level Boundaries, and Phylogenetic Analyses of the Family Rhacophoridae: a Review and Present Day Status
Contemporary Herpetology ISSN 1094-2246 2000 Number 2 7 April 2000 CHARACTER ASSESSMENT, GENUS LEVEL BOUNDARIES, AND PHYLOGENETIC ANALYSES OF THE FAMILY RHACOPHORIDAE: A REVIEW AND PRESENT DAY STATUS Jeffery A. Wilkinson ([email protected]) and Robert C. Drewes ([email protected]) Department of Herpetology, California Academy of Sciences, Golden Gate Park, San Francisco, California 94118 Abstract. The first comprehensive phylogenetic analysis of the family Rhacophoridae was conducted by Liem (1970) scoring 81 species for 36 morphological characters. Channing (1989), in a reanalysis of Liem’s study, produced a phylogenetic hypothesis different from that of Liem. We compared the two studies and produced a third phylogenetic hypothesis based on the same characters. We also present the synapomorphic characters from Liem that define the major clades and each genus within the family. Finally, we summarize intergeneric relationships within the family as hypothesized by other studies, and the family’s current status as it relates to other ranoid families. The family Rhacophoridae is comprised of over 200 species of Asian and African tree frogs that have been categorized into 10 genera and two subfamilies (Buergerinae and Rhacophorinae; Duellman, 1993). Buergerinae is a monotypic category that accommodates the relatively small genus Buergeria. The remaining genera, Aglyptodactylus, Boophis, Chirixalus, Chiromantis, Nyctixalus, Philautus, Polyp edates, Rhacophorus, and Theloderma, comprise Rhacophorinae (Channing, 1989). The family is part of the neobatrachian clade Ranoidea, which also includes the families Ranidae, Hyperoliidae, Dendrobatidae, Arthroleptidae, the genus Hemisus, and possibly the family Microhylidae. The Ranoidea clade is distinguished from other neobatrachians by the synapomorphic characters of completely fused epicoracoid cartilages, the medial end of the coracoid being wider than the lateral end, and the insertion of the semitendinosus tendon being dorsal to the m. -
Buergeria Japonica) Tadpoles from Island Populations
Volume 26 (July 2016), 207–211 FULL PAPER Herpetological Journal Published by the British Salinity and thermal tolerance of Japanese stream tree Herpetological Society frog (Buergeria japonica) tadpoles from island populations Shohei Komaki1, 2, Takeshi Igawa1, 2, Si-Min Lin3 & Masayuki Sumida2 1Division of Developmental Science, Graduate School of International Development and Cooperation, Hiroshima University, Hiroshima, Japan 2Institute for Amphibian Biology, Graduate School of Science, Hiroshima University, Hiroshima, Japan 3Department of Life Science, National Taiwan Normal University, Taipei, Taiwan Physiological tolerance to variable environmental conditions is essential for species to disperse over habitat boundaries and sustain populations in new habitats. In particular, salinity and temperature are one of the major factors determining species’ distributions. The tree frog Buergeria japonica is the most widely distributed amphibian species found in the Ryukyu Archipelago in Japan and Taiwan, and uses a wide range of breeding sites. Such characteristics suggest a high salinity and thermal tolerance in B. japonica tadpoles. We measured the salinity and thermal tolerance of tadpoles from three islands to determine if physiological tolerance could have contributed to the wide dispersal and survival across different environments. The critical salinity of B. japonica was 10–11‰, a value markedly below seawater. We also observed a critical maximum temperature of approximately 40°C, a value which is higher than what is commonly observed -
336 Natural History Notes
336 NATURAL HISTORY NOTES in an introduced population in Florida, USA (Patrovic 1973. J. kuvangensis (Channing and Howell. 2003. Herpetol. Rev. 34:51– Herpetol. 7:49–51). The frog observed by Patrovic (1973, op. cit.) 52), Kassina lamottei (Rödel et al. 2000, op. cit.), and Kassina also had melanin on the dorsal skin between the eyes but its eyes maculata (Liedtke and Müller 2012. Herpetol. Notes. 5:309– were pink. 310). Here we report observations of death–feigning for two We thank the Environment Conservation Fund and the Hong additional Kassina species: K. maculosa and K. arboricola. On Kong Government for supporting this work. 23 May 2018, we observed death-feigning behavior exhibited by HO-NAM NG, FRANCO KA-WAH LEUNG and WING-HO LEE, K. maculosa, while surveying a small forest patch on the Batéké Department of Biology, Hong Kong Baptist University, Hong Kong SAR, Plateau in Lekety Village, Cuvette department, Republic of Congo China; YIK-HEI SUNG, Division of Ecology and Biodiversity, School of (1.59216°S, 14.95787°E; WGS 84; 381 m elev.). After hand capturing Biological Sciences, The University of Hong Kong (e-mail: heisyh@gmail. the individual, it curled into a ball and remained immobile (Fig. com). 1A); this was the only individual out of six who exhibited this response. This specimen is deposited at the Florida Museum of FEJERVARYA LIMNOCHARIS (Asian Rice Frog). DIET. Anurans Natural History (UF 185502). This is also the first country record are generalist feeders and in most cases gape-limited foragers. of K. maculosa for the Republic of Congo. -
Fundamental Experiments to Develop Eco-Friendly Techniques for Conserving Frog Habitat in Paddy Areas Escape Countermeasures for Frogs Falling Into Agricultural Concrete Canals
JARQ 44 (4), 405 – 413 (2010) http://www.jircas.affrc.go.jpFundamental Experiment of Eco-friendly Techniques for Frogs in Paddy Areas Fundamental Experiments to Develop Eco-friendly Techniques for Conserving Frog Habitat in Paddy Areas: Escape Countermeasures for Frogs Falling into Agricultural Concrete Canals Keiji WATABE*, Atsushi MORI, Noriyuki KOIZUMI and Takeshi TAKEMURA Department of Rural Environment, National Institute for Rural Engineering, National Agriculture and Food Research Organization (Tsukuba, Ibaraki 305–8609, Japan) Abstract Frogs often drown in agricultural canals with deep concrete walls that are installed commonly in paddy areas after land consolidation projects in Japan because they cannot escape after falling into the canal. We propose a partial concrete canal with gently sloped walls as a countermeasure for frogs to escape the canal and investigated the preferable angle of the sloped walls, water depth and flow ve- locity for Rana porosa porosa. Our experiments showed that only 13 individuals (2%) escaped by leaping out of the canal, indicating that climbing up is the main escape behavior of R. p. porosa. Walls with slopes of 30–45 degrees allowed 50–60% of frogs to escape from experimental canals, the frogs especially easily climbed up walls with a 30 degree slope. Adjusting water depth to 5 cm or more would assist the frogs in reaching the escape countermeasures because at such depths frogs are not able to stand on the canal bottom and to move freely about. Flow velocity should be slower around the countermeasures because R. p. porosa is not good at long-distance swimming and cannot remain under running water for a long time. -
Eastern Dwarf Treefrog (Litoria Fallax) 1 Native Range and Status in the United States
Eastern Dwarf Treefrog (Litoria fallax) Ecological Risk Screening Summary U.S. Fish & Wildlife Service, May 2012 Revised, March 2017 Web Version, 2/9/2018 Photo: Michael Jefferies. Licensed under CC BY-NC. Available: http://eol.org/data_objects/25762625. (March 2017). 1 Native Range and Status in the United States Native Range From Hero et al. (2009): “This Australian species occurs along the coast and in adjacent areas from Cairns in northern Queensland south to southern New South Wales, including Fraser Island.” Status in the United States From Hero et al. (2009): “Guam” 1 Means of Introductions in the United Status From Christy et al. (2007): “The initial specimen of the now-established species L. fallax was discovered in the central courtyard of Guam’s International Airport in 1968 (Falanruw, 1976), leading Eldredge (1988) to speculate that the species was brought to Guam on board an aircraft. Aircraft and maritime vessels entered Guam from Australia, the home range of the species (Cogger, 2000) during the late 1960s, although documentation with respect to the frequency of these arrivals and the types of commodities shipped is difficult to obtain. It is therefore unclear whether the Guam population is the result of released pets, stowaways onboard a transport vessel, or stowaways in suitable cargo such as fruit or vegetables.” Remarks From GBIF (2016): “BASIONYM Hylomantis fallax Peters, 1880” 2 Biology and Ecology Taxonomic Hierarchy and Taxonomic Standing From ITIS (2017): “Kingdom Animalia Subkingdom Bilateria Infrakingdom Deuterostomia Phylum Chordata Subphylum Vertebrata Infraphylum Gnathostomata Superclass Tetrapoda Class Amphibia Order Anura Family Hylidae Subfamily Pelodryadinae Genus Litoria Species Litoria fallax (Peters, 1880)” “Current Standing: valid” Size, Weight, and Age Range From Atlas of Living Australia (2017): “Up to less than 30mm” 2 Environment From Hero et al. -
3Systematics and Diversity of Extant Amphibians
Systematics and Diversity of 3 Extant Amphibians he three extant lissamphibian lineages (hereafter amples of classic systematics papers. We present widely referred to by the more common term amphibians) used common names of groups in addition to scientifi c Tare descendants of a common ancestor that lived names, noting also that herpetologists colloquially refer during (or soon after) the Late Carboniferous. Since the to most clades by their scientifi c name (e.g., ranids, am- three lineages diverged, each has evolved unique fea- bystomatids, typhlonectids). tures that defi ne the group; however, salamanders, frogs, A total of 7,303 species of amphibians are recognized and caecelians also share many traits that are evidence and new species—primarily tropical frogs and salaman- of their common ancestry. Two of the most defi nitive of ders—continue to be described. Frogs are far more di- these traits are: verse than salamanders and caecelians combined; more than 6,400 (~88%) of extant amphibian species are frogs, 1. Nearly all amphibians have complex life histories. almost 25% of which have been described in the past Most species undergo metamorphosis from an 15 years. Salamanders comprise more than 660 species, aquatic larva to a terrestrial adult, and even spe- and there are 200 species of caecilians. Amphibian diver- cies that lay terrestrial eggs require moist nest sity is not evenly distributed within families. For example, sites to prevent desiccation. Thus, regardless of more than 65% of extant salamanders are in the family the habitat of the adult, all species of amphibians Plethodontidae, and more than 50% of all frogs are in just are fundamentally tied to water. -
Wiens Et Al. Page: 1
Wiens et al. page: 1 1 Supporting Information 2 Appendix S1 3 Expanded Materials and Methods 4 Appendix S1.A. Local Sites. We obtained data on the local species composition 5 of 123 sites throughout the range of Hylidae (Tables S1–S3). Our major source of 6 data was published studies of the amphibian faunas of local sites. We focused on 7 well-studied site, typically of several km2 in size, that represent a single biome or 8 habitat (e.g. tropical lowland rainforest), but include multiple microhabitats (e.g. 9 forest, stream edge, pond). We generally excluded sites spanning multiple 10 biomes, and from poorly known regions in which the observed hylid richness 11 was much lower than for other sites in the same region (possibly reflecting poor 12 sampling or human impacts). In some cases, we also included species lists from 13 national parks or reserves, particularly for regions where we could corroborate 14 these lists with published range maps (e.g. U.S., Australia). For some areas 15 having few obvious sites, we picked localities where large numbers of hylid 16 species have been collected, based on literature or museum records. For areas 17 with very low hylid diversity (e.g., Europe, Asia, Western North America), we 18 used museum records. 19 For most analyses, we used a single, well-studied locality to represent 20 each major biogeographic region (Table 1), in order to reduce potential problems 21 of uneven numbers of sites among biogeographic regions, spatial 22 autocorrelation, and inadequately surveyed sites. For a given region, we used Wiens et al. -
Globally Important Agricultural Heritage Systems (GIAHS) Application
Globally Important Agricultural Heritage Systems (GIAHS) Application SUMMARY INFORMATION Name/Title of the Agricultural Heritage System: Osaki Kōdo‟s Traditional Water Management System for Sustainable Paddy Agriculture Requesting Agency: Osaki Region, Miyagi Prefecture (Osaki City, Shikama Town, Kami Town, Wakuya Town, Misato Town (one city, four towns) Requesting Organization: Osaki Region Committee for the Promotion of Globally Important Agricultural Heritage Systems Members of Organization: Osaki City, Shikama Town, Kami Town, Wakuya Town, Misato Town Miyagi Prefecture Furukawa Agricultural Cooperative Association, Kami Yotsuba Agricultural Cooperative Association, Iwadeyama Agricultural Cooperative Association, Midorino Agricultural Cooperative Association, Osaki Region Water Management Council NPO Ecopal Kejonuma, NPO Kabukuri Numakko Club, NPO Society for Shinaimotsugo Conservation , NPO Tambo, Japanese Association for Wild Geese Protection Tohoku University, Miyagi University of Education, Miyagi University, Chuo University Responsible Ministry (for the Government): Ministry of Agriculture, Forestry and Fisheries The geographical coordinates are: North latitude 38°26’18”~38°55’25” and east longitude 140°42’2”~141°7’43” Accessibility of the Site to Capital City of Major Cities ○Prefectural Capital: Sendai City (closest station: JR Sendai Station) ○Access to Prefectural Capital: ・by rail (Tokyo – Sendai) JR Tohoku Super Express (Shinkansen): approximately 2 hours ※Access to requesting area: ・by rail (closest station: JR Furukawa -
Mating Strategy and Breeding Patterns of the Foothill Yellow-Legged Frog (Rana Boylii)
Herpetological Conservation and Biology 3(2):128-142 Submitted: 15 October 2007; Accepted: 29 March 2008 MATING STRATEGY AND BREEDING PATTERNS OF THE FOOTHILL YELLOW-LEGGED FROG (RANA BOYLII) 1,2 2 CLARA A. WHEELER AND HARTWELL H. WELSH, JR. 1Department of Wildlife, Humboldt State University, Arcata, CA 95521, USA, e-mail: [email protected] 2USDA Pacific Southwest Research Station, 1700 Bayview Dr., Arcata, CA 95521, USA Abstract.—The Foothill Yellow-legged Frog (Rana boylii) has declined across much of its native range in California. Improper stream management may lower egg mass survival and reduce the availability of suitable breeding habitats. We collected data during six breeding-seasons (2002-2007) along an unregulated stream in northwestern California. We monitored temporal reproductive patterns at a breeding site and used mark-recapture and behavioral observations to spatially and temporally track individuals and investigate aspects of the mating strategy. The duration of breeding activity lasted three to seven and a half weeks. Day within the breeding-season and stream flow influenced breeding activity. Male frogs congregated at the breeding site during the reproductive season but females arrived asynchronously. Male frogs showed fidelity to individual sites within the breeding area. The daily operational sex ratio of adults was male- biased, while the overall breeding-season operational sex ratio was female-biased. Males in amplexus were larger than males never observed in amplexus, providing evidence of a non-random mating pattern. These frogs showed plasticity in temporal breeding patterns and were not exclusively prolonged or explosive breeders. Frog behaviors at the breeding site were more typical of prolonged breeding anurans. -
1704632114.Full.Pdf
Phylogenomics reveals rapid, simultaneous PNAS PLUS diversification of three major clades of Gondwanan frogs at the Cretaceous–Paleogene boundary Yan-Jie Fenga, David C. Blackburnb, Dan Lianga, David M. Hillisc, David B. Waked,1, David C. Cannatellac,1, and Peng Zhanga,1 aState Key Laboratory of Biocontrol, College of Ecology and Evolution, School of Life Sciences, Sun Yat-Sen University, Guangzhou 510006, China; bDepartment of Natural History, Florida Museum of Natural History, University of Florida, Gainesville, FL 32611; cDepartment of Integrative Biology and Biodiversity Collections, University of Texas, Austin, TX 78712; and dMuseum of Vertebrate Zoology and Department of Integrative Biology, University of California, Berkeley, CA 94720 Contributed by David B. Wake, June 2, 2017 (sent for review March 22, 2017; reviewed by S. Blair Hedges and Jonathan B. Losos) Frogs (Anura) are one of the most diverse groups of vertebrates The poor resolution for many nodes in anuran phylogeny is and comprise nearly 90% of living amphibian species. Their world- likely a result of the small number of molecular markers tra- wide distribution and diverse biology make them well-suited for ditionally used for these analyses. Previous large-scale studies assessing fundamental questions in evolution, ecology, and conser- used 6 genes (∼4,700 nt) (4), 5 genes (∼3,800 nt) (5), 12 genes vation. However, despite their scientific importance, the evolutionary (6) with ∼12,000 nt of GenBank data (but with ∼80% missing history and tempo of frog diversification remain poorly understood. data), and whole mitochondrial genomes (∼11,000 nt) (7). In By using a molecular dataset of unprecedented size, including 88-kb the larger datasets (e.g., ref. -
Phylogenetics, Classification, and Biogeography of the Treefrogs (Amphibia: Anura: Arboranae)
Zootaxa 4104 (1): 001–109 ISSN 1175-5326 (print edition) http://www.mapress.com/j/zt/ Monograph ZOOTAXA Copyright © 2016 Magnolia Press ISSN 1175-5334 (online edition) http://doi.org/10.11646/zootaxa.4104.1.1 http://zoobank.org/urn:lsid:zoobank.org:pub:D598E724-C9E4-4BBA-B25D-511300A47B1D ZOOTAXA 4104 Phylogenetics, classification, and biogeography of the treefrogs (Amphibia: Anura: Arboranae) WILLIAM E. DUELLMAN1,3, ANGELA B. MARION2 & S. BLAIR HEDGES2 1Biodiversity Institute, University of Kansas, 1345 Jayhawk Blvd., Lawrence, Kansas 66045-7593, USA 2Center for Biodiversity, Temple University, 1925 N 12th Street, Philadelphia, Pennsylvania 19122-1601, USA 3Corresponding author. E-mail: [email protected] Magnolia Press Auckland, New Zealand Accepted by M. Vences: 27 Oct. 2015; published: 19 Apr. 2016 WILLIAM E. DUELLMAN, ANGELA B. MARION & S. BLAIR HEDGES Phylogenetics, Classification, and Biogeography of the Treefrogs (Amphibia: Anura: Arboranae) (Zootaxa 4104) 109 pp.; 30 cm. 19 April 2016 ISBN 978-1-77557-937-3 (paperback) ISBN 978-1-77557-938-0 (Online edition) FIRST PUBLISHED IN 2016 BY Magnolia Press P.O. Box 41-383 Auckland 1346 New Zealand e-mail: [email protected] http://www.mapress.com/j/zt © 2016 Magnolia Press All rights reserved. No part of this publication may be reproduced, stored, transmitted or disseminated, in any form, or by any means, without prior written permission from the publisher, to whom all requests to reproduce copyright material should be directed in writing. This authorization does not extend to any other kind of copying, by any means, in any form, and for any purpose other than private research use. -
Distribution and Genetic Diversity of the Amphibian Chytrid in Japan
Journal of Fungi Article Distribution and Genetic Diversity of the Amphibian Chytrid in Japan Koichi Goka 1,*, Jun Yokoyama 2 and Atsushi Tominaga 3 1 National Institute for Environmental Studies, 16-2 Onogawa, Tsukuba 305-8506, Japan 2 Department of Biology, Faculty of Sciences, Yamagata University, 1-4-12 Kojirakawa, Yamagata-shi, Yamagata 990-8560, Japan; [email protected] 3 Department of Natural Sciences, Faculty of Education, University of the Ryukyus, 1 Senbaru, Nishihara, Okinawa 901-0213, Japan; [email protected] * Correspondence: [email protected]; Tel.: +81-29-850-2480; Fax: +81-29-850-2582 Abstract: While research on frog chytrid fungus Batrachochytrium dendrobatidis (Bd), an infectious disease that threatens amphibian diversity, continues to advance worldwide, little progress has been made in Japan since around 2010. The reason for this is, which we pointed out in 2009, that the origin of frog chytrid fungus may be in the East Asian region, including Japan based on the Bd ITS-DNA variation, and as few cases of mass mortality caused by this fungus have been observed in wild amphibian populations in Japan, the interest of the Japanese government and the general public in Bd has waned. However, we believe that organizing the data obtained so far in Japan and distributing the status of frog chytrid fungus in Japan to the world will provide useful insight for future risk management of this pathogen. We collected more than 5500 swab samples from wild amphibians throughout Japan from 2009 to 2010. Then, we investigated the infection status using the Nested-PCR method.