Applying Critical Thinking to the Amphibian Decline Problem
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The New Age of Extinction
Wednesday, Apr. 01, 2009 The New Age of Extinction By Bryan Walsh / Madagascar There are at least 8 million unique species of life on the planet, if not far more, and you could be forgiven for believing that all of them can be found in Andasibe. Walking through this rain forest in Madagascar is like stepping into the library of life. Sunlight seeps through the silky fringes of the Ravenea louvelii, an endangered palm found, like so much else on this African island, nowhere else. Leaf-tailed geckos cling to the trees, cloaked in green. A fat Parson's chameleon lies lazily on a branch, beady eyes scanning for dinner. But the animal I most hoped to find, I don't see at first; I hear it, though — a sustained groan that electrifies the forest quiet. My Malagasy guide, Marie Razafindrasolo, finds the source of the sound perched on a branch. It is the black-and-white indri, largest of the lemurs — a type of small primate found only in Madagascar. The cry is known as a spacing call, a warning to other indris to keep their distance, to prevent competition for food. But there's not much risk of interlopers. The species — like many other lemurs, like many other animals in Madagascar, like so much of life on Earth — is endangered and dwindling fast. Madagascar — which separated from India 80 million to 100 million years ago before eventually settling off the southeastern coast of Africa — is in many ways an Earth apart. All that time in geographic isolation made Madagascar a Darwinian playground, its animals and plants evolving into forms utterly original. -
Newsletter V5-N2
V irg in ia Herpetological Society August 1995 Volume 5, Number 2 NEWSLETTER Catesheiana Co-editors President Paul W. Saltier Ron Southwick R. Terry Spohn Paul Sattler - Pres. Elect Newsletter Editor Sccrctarv/Trcasurcr Mike Finder Bob Hogan microdistribution patterns of Worldwide Amphibian Decline salamanders in terrestrial environments Is There a Virginia Connection? (Wyman and Hawksley-Lescault, 1987). Increased ultraviolet radiation, apparently due to the thinning of the Submitted by Joseph C. Mitchell, Department of Biology, ozone layer, has been shown to k ill University o f Richmond, Richmond, VA 23173 developing eggs of the Cascades frog (Rana cascadae) and western toad (Bufo boreas) (Blaustein et al., 1994a). Amphibians have received Congress of Herpetology held in The widespread fungus (Saprolegnia considerable media and scientific Canterbury, England in 1989. ferax) introduced into ponds and lakes attention over the past half dozen years Pin-pointing the causes of in the Pacific northwest by introduced because of species extinctions and these problems has been elusive. Early fish has caused egg mortality in the population declines worldwide. on, scientists were looking for one western toad (Blaustein et al., 1994b). Observations such as (1) the last global smoking gun, but the results of An unidentified virus carried by individual of the Australian gastric studies that have been published since introduced fish, such as tilapia, brooding frog (Rheobatrachus silus) the alarm surfaced indicate that the guppies, and carp, is suspected as was seen in 1979 (Tyler and Davies, causes are varied and often local. The causing frog decline in Australia 1985); (2) the golden toad (Bufo most common cause of local population (Anderson, 1995). -
Table 7: Species Changing IUCN Red List Status (2018-2019)
IUCN Red List version 2019-3: Table 7 Last Updated: 10 December 2019 Table 7: Species changing IUCN Red List Status (2018-2019) Published listings of a species' status may change for a variety of reasons (genuine improvement or deterioration in status; new information being available that was not known at the time of the previous assessment; taxonomic changes; corrections to mistakes made in previous assessments, etc. To help Red List users interpret the changes between the Red List updates, a summary of species that have changed category between 2018 (IUCN Red List version 2018-2) and 2019 (IUCN Red List version 2019-3) and the reasons for these changes is provided in the table below. IUCN Red List Categories: EX - Extinct, EW - Extinct in the Wild, CR - Critically Endangered [CR(PE) - Critically Endangered (Possibly Extinct), CR(PEW) - Critically Endangered (Possibly Extinct in the Wild)], EN - Endangered, VU - Vulnerable, LR/cd - Lower Risk/conservation dependent, NT - Near Threatened (includes LR/nt - Lower Risk/near threatened), DD - Data Deficient, LC - Least Concern (includes LR/lc - Lower Risk, least concern). Reasons for change: G - Genuine status change (genuine improvement or deterioration in the species' status); N - Non-genuine status change (i.e., status changes due to new information, improved knowledge of the criteria, incorrect data used previously, taxonomic revision, etc.); E - Previous listing was an Error. IUCN Red List IUCN Red Reason for Red List Scientific name Common name (2018) List (2019) change version Category -
The Puzzling Golden Toad Crack the Puzzle and Reveal the Secret Word Activity Guide
The Puzzling Golden Toad Crack the puzzle and reveal the secret word Activity Guide Did you know that the specific effects of climate change on animals are still unknown? Meet the golden toad and learn why scientists are still puzzled by his mysterious disappearance. Try This! Step 1: Set up the time line sheet. Step 2: Find the seven puzzle pieces and read the information on each. Step 3: Organize the time line to reveal the secret word. How do you think scientists study the effect of climate change on species such as the Golden Toad? Climate Connection The effect of climate change on species is still unknown and widely debated. Scientists believe that factors such as increased droughts and the spread of a fungus may have led to the demise of the Golden Toad. The number of Golden Toads people saw declined from 1,500 to zero in such a short period of time. Scientists suspect that conditions related to climate change was the reason for their extinction. Turn the page over to learn more! Sciencenter, Ithaca, NY Page 1 www.sciencenter.org The Puzzling Golden Toad Activity Guide What’s Happening? The Golden Toad (Bufo periglenes) was an amphibian only found in areas near the Monteverde Cloud Forest Preserve in Costa Rica. This species strangely disappeared in the late 1980’s, which led to extensive studies on what caused the extinction of this species. After studying the drastic manner in which this species declined, scientists started to suspect that climate change was the reason for their extinction. Scientists began to study how stress relating to moisture, temperature, diseases and contaminants in combination with climate change could have affected the Golden Toad. -
The IUCN Amphibians Initiative: a Record of the 2001-2008 Amphibian Assessment Efforts for the IUCN Red List
The IUCN Amphibians Initiative: A record of the 2001-2008 amphibian assessment efforts for the IUCN Red List Contents Introduction ..................................................................................................................................... 4 Amphibians on the IUCN Red List - Home Page ................................................................................ 5 Assessment process ......................................................................................................................... 6 Partners ................................................................................................................................................................. 6 The Central Coordinating Team ............................................................................................................................ 6 The IUCN/SSC – CI/CABS Biodiversity Assessment Unit........................................................................................ 6 An Introduction to Amphibians ................................................................................................................................. 7 Assessment methods ................................................................................................................................................ 7 1. Data Collection .................................................................................................................................................. 8 2. Data Review ................................................................................................................................................... -
Two New Harlequin Frogs (Anura: Atelopus) from the Andes of Northern Peru Pablo J
Southern Illinois University Carbondale OpenSIUC Publications Department of Zoology 2008 Two New Harlequin Frogs (Anura: Atelopus) from the Andes of Northern Peru Pablo J. Venegas Alessandro Catenazzi Southern Illinois University Carbondale, [email protected] Karen Siu Ting Jorge Carrillo Follow this and additional works at: http://opensiuc.lib.siu.edu/zool_pubs Published in Salamandra , Issue 44 (2008) at http://www.salamandra-journal.com/ index.php?option=com_docman&Itemid=66 Recommended Citation Venegas, Pablo J., Catenazzi, Alessandro, Siu Ting, Karen and Carrillo, Jorge. "Two New Harlequin Frogs (Anura: Atelopus) from the Andes of Northern Peru." (Jan 2008). This Article is brought to you for free and open access by the Department of Zoology at OpenSIUC. It has been accepted for inclusion in Publications by an authorized administrator of OpenSIUC. For more information, please contact [email protected]. Two new harlequin frogs from Peru SALAMANDRA 44 3 163-176 Rheinbach, 20 August 2008 ISSN 0036-3375 Two new harlequin frogs (Anura: Atelopus) from the Andes of northern Peru Pablo J. Venegas, Alessandro Catenazzi, Karen Siu-Ting & Jorge Carrillo Abstract. Two new species of Atelopus (harlequin frogs) are described from the Andes of northern Peru, one from the northern Cordillera de Huancabamba (Departamento de Piura), 2,950 m elevation, and the other from an inter-Andean valley of the upper Marañon basin, Cordillera Central (Departamento de La Libertad), 2,620 m elevation. We also suggest the possible link between infection by the chytrid fungus and mortality of harlequin frogs in the upper Marañon basin in 999. Key words. Bufonidae, Atelopus patazensis sp. -
Golden Toad Fact Sheet
Golden Toad Fact Sheet Common Name: Golden Toad Scientific Name: Incilius periglenes, formerly Bufo periglenes Wild Status: Extinct Habitat: Cloud Forest Country: Costa Rica Shelter: Underground Life Span: Estimated 10 Years Size: 3 inches approx Details The golden toad is one of the many victims of global decline in amphibians. The causes are not well understood for amphibians or for the golden toad. Because golden toads laid many eggs in shallow pools, some speculate a drought harmed the toad population. Others believe it may be a combination of climate change, air pollution, and disease. As amphibian populations continue to decline, biologists look to the case of the golden toad as a sign of what could happen not just to toads, but any cold blooded creature sensitive to its surroundings. Cool Facts • Like many other toads, this species spent much of its life underground, waiting for the rain. • Was found only in Costa Rica in what is called a "cloud forest" due to the constant, cloudy fog. • Females were bigger than males and came in a variety of colors. Males were usually golden in color. • Unlike cane toads, the golden toads did not have poison • The last golden toad was seen in 1989. In 2004, it was considered extinct. Taxonomic Breakdown Kingdom: Animalia Phylum: Chordata Class: Amphibia Order: Anura Family: Bufonidae Genus: Incilius Species: I. periglenes Conservation & Helping Although the toads were closely examined and counted each year, scientists were not able to stop the decline of the toad, and they are considered extinct. Their average lifespan are just over 10 years, and no golden toads have been seen in decades. -
Yosemite Toad Conservation Assessment
United States Department of Agriculture YOSEMITE TOAD CONSERVATION ASSESSMENT A Collaborative Inter-Agency Project Forest Pacific Southwest R5-TP-040 January Service Region 2015 YOSEMITE TOAD CONSERVATION ASSESSMENT A Collaborative Inter-Agency Project by: USDA Forest Service California Department of Fish and Wildlife National Park Service U.S. Fish and Wildlife Service Technical Coordinators: Cathy Brown USDA Forest Service Amphibian Monitoring Team Leader Stanislaus National Forest Sonora, CA [email protected] Marc P. Hayes Washington Department of Fish and Wildlife Research Scientist Science Division, Habitat Program Olympia, WA Gregory A. Green Principal Ecologist Owl Ridge National Resource Consultants, Inc. Bothel, WA Diane C. Macfarlane USDA Forest Service Pacific Southwest Region Threatened Endangered and Sensitive Species Program Leader Vallejo, CA Amy J. Lind USDA Forest Service Tahoe and Plumas National Forests Hydroelectric Coordinator Nevada City, CA Yosemite Toad Conservation Assessment Brown et al. R5-TP-040 January 2015 YOSEMITE TOAD WORKING GROUP MEMBERS The following may be the contact information at the time of team member involvement in the assessment. Becker, Dawne Davidson, Carlos Harvey, Jim Associate Biologist Director, Associate Professor Forest Fisheries Biologist California Department of Fish and Wildlife Environmental Studies Program Humboldt-Toiyabe National Forest 407 West Line St., Room 8 College of Behavioral and Social Sciences USDA Forest Service Bishop, CA 93514 San Francisco State University 1200 Franklin Way (760) 872-1110 1600 Holloway Avenue Sparks, NV 89431 [email protected] San Francisco, CA 94132 (775) 355-5343 (415) 405-2127 [email protected] Boiano, Daniel [email protected] Aquatic Ecologist Holdeman, Steven J. Sequoia/Kings Canyon National Parks Easton, Maureen A. -
Predator-Prey Interactions Between Hellbenders
PREDATOR-PREY INTERACTIONS BETWEEN HELLBENDERS (CRYPTOBRANCHUS ALLEGANIENSIS ALLEGANIENSIS AND C. A. BISHOPI) AND NATIVE AND NONNATIVE FISHES A Thesis Presented to The Graduate College of Missouri State University In Partial Fulfillment Of the Requirements for the Degree Master of Science, Biology By Brian G. Gall August 2008 PREDATOR-PREY INTERACTIONS BETWEEN HELLBENDERS (CRYPTOBRANCHUS ALLEGANIENSIS ALLEGANIENSIS AND C. A. BISHOPI) AND NATIVE AND NONNATIVE FISHES Department of Biology Missouri State University, August 2008 Masters of Science Brian G. Gall ABSTRACT The introduction of nonnative fishes often results in the local extinction of native amphibians due to a lack of evolutionary history and therefore, minimally-adapted antipredator behaviors toward the introduced fishes. Populations of hellbenders (Cryptobranchus alleganiensis) in Missouri have declined considerably since the 1980’s, coinciding with a rapid increase in trout introductions for recreational angling. I examined hellbender and fish predator-prey interactions by: (1) examining the foraging behavior of predatory fishes in response to a hellbender secretion; (2) comparing the number of secretion and control-soaked food pellets consumed by trout; and (3) comparing the response of larval hellbenders to chemical stimuli from introduced (trout) and native fish predators. Brown trout, walleye and large banded sculpin respond to hellbender secretions with increased activity while small banded sculpin responded by decreasing activity. In addition, brown trout ingested more hellbender secretion-soaked food pellets than control pellets, while rainbow trout expelled secretion-soaked food pellets. Finally, larval hellbenders exhibited weak fright behavior in response to chemical stimuli from nonnative trout relative to their responses to native predatory fish stimuli. These combinations of responses indicate that predation by nonnative fishes may be a plausible hypothesis for the decline of hellbender populations in Missouri. -
Research Article Assessing the Molecular Phylogeny of a Near Extinct Group of Vertebrates: the Neotropical Harlequin Frogs (Bufonidae; Atelopus)
Systematics and Biodiversity (2011), 9(1):45–57 Research Article Assessing the molecular phylogeny of a near extinct group of vertebrates: the Neotropical harlequin frogs (Bufonidae; Atelopus) STEFAN LOTTERS¨ 1,ARIEVANDERMEIJDEN2,LUISA.COLOMA3,RENAUDBOISTEL4,PETERCLOETENS4, RAFFAEL ERNST5,EDGARLEHR6 &MICHAELVEITH1 1Trier University, Department of Biogeography, Universitatsring¨ 15, 54286 Trier, Germany 2CIBIO, Centro de Investigac¸ao˜ em Biodiversidade e Recursos Geneticos,´ Campus Agrario´ de Vairao,˜ 4485-661, Vairao,˜ Portugal 3Centro de Investigacion´ y Conservacion´ de Anfibios, Giovanni Farina 566, San Rafael, Quito, Ecuador 4iPHEP-UMR CNRS 6046, UFR SFA Universite´ de Poitiers, 40 avenue du Recteur Pineau, 86022 Poitiers, France 5Museum of Zoology, Senckenberg Natural History Collections Dresden, A. B. Meyer Building, 01109 Dresden, Germany 6Illinois Wesleyan University, Department of Biology, PO BOX 2900, Bloomington, IL 61702-2900, USA (Received 4 May 2010; revised 17 January 2011; accepted 19 January 2011; printed 30 March 2011) Neotropical harlequin frogs, Atelopus,areaspecies-richbufonidgroup.Atelopus monophyly has been suggested but intergeneric, interspecific and intraspecific relationships are poorly understood. One reason is that morphological characters of harlequin frogs are often difficult to interpret, making species delimitations difficult. Molecular analyses (DNA barcoding, phylogeny) may be helpful but sampling is hampered as most of the more than 100 Atelopus species have undergone severe population declines and many are possibly extinct. We processed mitochondrial DNA (12S and 16S rRNA) of 28 available ingroup samples from a large portion of the genus’ geographic range (Bayesian Inference, Maximum Likelihood). Our samples constitute a monophyletic unit, which is sister to other bufonid genera studied including the Andean genus Osornophryne. In contrast to previous morphological studies, our results suggest that Osornophryne is neither sister to Atelopus nor nested within it. -
Global Amphibian Declines Houlahan Et Al
Amphibian Population Declines and Malformations Extinct, 1989 Bufo periglenes, CR Hyla regilla, OR Matthew J. Gray University of Tennessee Worldwide Amphibian Population Declines Global Amphibian Declines Houlahan et al. 2000, Nature 404:752–755 North America Western Europe 250 300 s 200 250 200 150 150 100 100 50 50 Number of Populations Number of Population 0 0 1960 1963 1966 1969 1972 1975 1978 1981 1984 1987 1990 1993 1996 1960 1963 1966 1969 1972 1975 1978 1981 1984 1987 1990 1993 1996 1 History of Amphibian Declines Prior 1970s: •Few extinctions; some localized die-offs Ohio Journal of Science 49:70-71 1970-mid-1980s: •Few extinctions •Localized die-offs in temperate areas associated with habitat destruction Alberta Naturalist 11:1-4 Late 80s-Now: •Increase in extinctions •Localized & regional die-offs in temperate and tropical areas; some in “pristine” areas Conservation Biology 7:355-362, 8:72-85, 10:406-413, 10:414-425, 12:106-117, 13:117-125; Biotropica 20:230-235; Nature 404:752-755 Status of Amphibian Populations United States: •1 Species Extinct (Rana fisheri) Western U.S. •10 Endangered; 7 Threatened; 8 Awaiting •CA = 6 Spp.; SE = 5 Spp.; Wyoming = 1 spp •SW = 6 Spp. (Chiracahua Leopard Frog, 80%) Puerto Rico: •3 Spp. Extinct (Golden, mottled, web-footed Coquis) 24 spp. (16 coquis) •1 Spp. of Toad; 2 Spp. Coquis 61% spp. in Caribbean Australia: •8 Spp. Extinct; 6 Spp. in Serious Decline Gastric-brooding Frogs Elevation (Discovered in ‘70s) Costa Rica: •1 Spp. Extinct (Golden toad) Pristine •Multiple in Decline Global Amphibian Distributions 2 Status of Amphibian Populations In Threat of 1/3 of amphibian species 43% in Extinction: 12% = birds, 23% = mammals decline Status of Amphibian Populations Greatest Percent (>80%) Largest number of species Status of Amphibian Populations Extinct Critically Endangered Data deficient Endangered Vulnerable Near Least Concern Threatened http://www.globalamphibians.org 3 Status of Amphibian Populations % Threaten Total EX EW CR EN VU NT LC DD ed or Order Table 1. -
Supporting Online Material For
www.sciencemag.org/cgi/content/full/science.1194442/DC1 Supporting Online Material for The Impact of Conservation on the Status of the World’s Vertebrates Michael Hoffmann,* Craig Hilton-Taylor, Ariadne Angulo, Monika Böhm, Thomas M. Brooks, Stuart H. M. Butchart, Kent E. Carpenter, Janice Chanson, Ben Collen, Neil A. Cox, William R. T. Darwall, Nicholas K. Dulvy, Lucy R. Harrison, Vineet Katariya, Caroline M. Pollock, Suhel Quader, Nadia I. Richman, Ana S. L. Rodrigues, Marcelo F. Tognelli, Jean-Christophe Vié, John M. Aguiar, David J. Allen, Gerald R. Allen, Giovanni Amori, Natalia B. Ananjeva, Franco Andreone, Paul Andrew, Aida Luz Aquino Ortiz, Jonathan E. M. Baillie, Ricardo Baldi, Ben D. Bell, S. D. Biju, Jeremy P. Bird, Patricia Black-Decima, J. Julian Blanc, Federico Bolaños, Wilmar Bolivar-G., Ian J. Burfield, James A. Burton, David R. Capper, Fernando Castro, Gianluca Catullo, Rachel D. Cavanagh, Alan Channing, Ning Labbish Chao, Anna M. Chenery, Federica Chiozza, Viola Clausnitzer, Nigel J. Collar, Leah C. Collett, Bruce B. Collette, Claudia F. Cortez Fernandez, Matthew T. Craig, Michael J. Crosby, Neil Cumberlidge, Annabelle Cuttelod, Andrew E. Derocher, Arvin C. Diesmos, John S. Donaldson, J. W. Duckworth, Guy Dutson, S. K. Dutta, Richard H. Emslie, Aljos Farjon, Sarah Fowler, Jörg Freyhof, David L. Garshelis, Justin Gerlach, David J. Gower, Tandora D. Grant, Geoffrey A. Hammerson, Richard B. Harris, Lawrence R. Heaney, S. Blair Hedges, Jean- Marc Hero, Baz Hughes, Syed Ainul Hussain, Javier Icochea M., Robert F. Inger, Nobuo Ishii, Djoko T. Iskandar, Richard K. B. Jenkins, Yoshio Kaneko, Maurice Kottelat, Kit M. Kovacs, Sergius L.