Tail Bifurcation in Plestiodon Skiltonianus
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REPTILIA: SQUAMATA: SCINCIDAE Eumeces Lagunensis Van Denburgh
792.1 REPTILIA: SQUAMATA: SCINCIDAE EUMECES LAGUNENSIS Catalogue of American Amphibians and Reptiles. Beaman, K.R., J.Q. Richmond, and L.L. Grismer. 2004. Eumeces lagunensis. Eumeces lagunensis Van Denburgh San Lucan Skink Eumeces skiltonianus: Yarrow 1882:41 (part). Eumeces lagunensis Van Denburgh 1895:134. Type locality, “San Francisquito, Sierra Laguna, [Baja California Sur, México].” Holotype, California Academy of Sciences (CAS) 400, collected by Gustav Eisen on 28 March 1892 (examined by LLG). See Remarks. Plestiodon lagunensis: Van Denburgh and Slevin 1921:52. Plestiodon skiltonianus lagunensis: Nelson 1921:114–115. Eumeces skiltonianus lagunensis: Linsdale 1932:374. • CONTENT. The species is monotypic. • DEFINITION. Eumeces lagunensis is a small skink with a maximum total length of 147 mm. The scutellation is as fol- lows: 24 scale rows at midbody; 57–60 dorsal scale rows; 40– 46 ventral scale rows; 102 subcaudals; 4 supraoculars (three touching frontal); frontonasal in contact with frontal or not; large interparietal enclosed posteriorly by medial contact of large parietals; 7–8 supralabials; upper secondary temporal in broad 0 100 200 km contact ventrally with last supralabial; 2 postmentals; 6 infralabials; 2 postlabials (not superimposed); 2–2 nuchals, oc- casionally 1–1, 1–2, or 3–3, blending posteriorly with wide, MAP. Range of Eumeces lagunensis, the white circle marks the type cycloid, imbricate, dorsal scales of body and tail; 16 scales locality, the gray circle marks the neotype locality, and dots indicate around base of tail; and vent bordered by two large scales ante- other records. riorly. Granular axillary scales are not prominent and only 0–2 short rows are present and situated posterior to the medial mar- gin of the forelimb insertion. -
Checklist Reptile and Amphibian
To report sightings, contact: Natural Resources Coordinator 980-314-1119 www.parkandrec.com REPTILE AND AMPHIBIAN CHECKLIST Mecklenburg County, NC: 66 species Mole Salamanders ☐ Pickerel Frog ☐ Ground Skink (Scincella lateralis) ☐ Spotted Salamander (Rana (Lithobates) palustris) Whiptails (Ambystoma maculatum) ☐ Southern Leopard Frog ☐ Six-lined Racerunner ☐ Marbled Salamander (Rana (Lithobates) sphenocephala (Aspidoscelis sexlineata) (Ambystoma opacum) (sphenocephalus)) Nonvenomous Snakes Lungless Salamanders Snapping Turtles ☐ Eastern Worm Snake ☐ Dusky Salamander (Desmognathus fuscus) ☐ Common Snapping Turtle (Carphophis amoenus) ☐ Southern Two-lined Salamander (Chelydra serpentina) ☐ Scarlet Snake1 (Cemophora coccinea) (Eurycea cirrigera) Box and Water Turtles ☐ Black Racer (Coluber constrictor) ☐ Three-lined Salamander ☐ Northern Painted Turtle ☐ Ring-necked Snake (Eurycea guttolineata) (Chrysemys picta) (Diadophis punctatus) ☐ Spring Salamander ☐ Spotted Turtle2, 6 (Clemmys guttata) ☐ Corn Snake (Pantherophis guttatus) (Gyrinophilus porphyriticus) ☐ River Cooter (Pseudemys concinna) ☐ Rat Snake (Pantherophis alleghaniensis) ☐ Slimy Salamander (Plethodon glutinosus) ☐ Eastern Box Turtle (Terrapene carolina) ☐ Eastern Hognose Snake ☐ Mud Salamander (Pseudotriton montanus) ☐ Yellow-bellied Slider (Trachemys scripta) (Heterodon platirhinos) ☐ Red Salamander (Pseudotriton ruber) ☐ Red-eared Slider3 ☐ Mole Kingsnake Newts (Trachemys scripta elegans) (Lampropeltis calligaster) ☐ Red-spotted Newt Mud and Musk Turtles ☐ Eastern Kingsnake -
Eumeces Gilberti Van Denburgh Gilbert's Skink
372.1 REPTILIA: SQUAMATA: SAURIA: SCINCIDAE EUMECES GILBERTI Catalogue of American Amphibians and Reptiles. Rodgers (1944) describes E. g. placerensis, and Lowe and Shannon (1954) E. g. arizonensis. Stebbins (1966) and Behler and King JONES,K. BRUCE. 1985. Eumeces gilberti. (1979) provide brief descriptions of the species. Eumeces gilberti Van Denburgh • ILLUSTRATIONS.Stebbins (1966) and Behler and King (1979) Gilbert's Skink provide color illustrations and color photographs of juveniles and adults, respectively. Black and white photographs appear in Van Denburgh (1922), Taylor (1935), and Smith (1946). Rodgers (1944) Eumeces gilberti: Van Denburgh, 1896:350. Type.locality, "Yo· provides a photograph of the type.specimen E. g. placerensis. Van semite Valley, Mariposa County, California." Holotype, Cali• Denburgh (1922), Taylor (1935), Smith (1946), and Rodgers and fornia Acad. Sci.-Stanford Univ. 4139, collected by Charles Fitch (1947) provide black and white illustrations with the latter H. Gilbert and James M. Hyde on 10-15 June 1896 (not the most detailed. examined by author). Eumeces skiltonianus: Cope, 1900:643 (part, by inference). • DISTRIBUTION.The species is distributed through central Cal• Eumeces skiltonianus: Camp, 1916:72-73 (part). ifornia, north approximately to the Yuba River, east through the Plestiodon skiltonianum: Grinnell and Camp, 1917:175, 176 (part). San Joaquin Valley to the Sierra Nevada, and west to the San Eumeces gilberti: Taylor, 1935:438. Resurrected name. Francisco Bay area. Its range extends southward along the Califor· nia coast (but at least 20 km inland) to San Diego, and into the • CONTENT.Five subspecies are recognized: gilberti, cancel• chaparral vegetation association of the San Pedro Martir of Baja losus, placerensis, rubricaudatus, and arizonensis. -
Literature Cited in Lizards Natural History Database
Literature Cited in Lizards Natural History database Abdala, C. S., A. S. Quinteros, and R. E. Espinoza. 2008. Two new species of Liolaemus (Iguania: Liolaemidae) from the puna of northwestern Argentina. Herpetologica 64:458-471. Abdala, C. S., D. Baldo, R. A. Juárez, and R. E. Espinoza. 2016. The first parthenogenetic pleurodont Iguanian: a new all-female Liolaemus (Squamata: Liolaemidae) from western Argentina. Copeia 104:487-497. Abdala, C. S., J. C. Acosta, M. R. Cabrera, H. J. Villaviciencio, and J. Marinero. 2009. A new Andean Liolaemus of the L. montanus series (Squamata: Iguania: Liolaemidae) from western Argentina. South American Journal of Herpetology 4:91-102. Abdala, C. S., J. L. Acosta, J. C. Acosta, B. B. Alvarez, F. Arias, L. J. Avila, . S. M. Zalba. 2012. Categorización del estado de conservación de las lagartijas y anfisbenas de la República Argentina. Cuadernos de Herpetologia 26 (Suppl. 1):215-248. Abell, A. J. 1999. Male-female spacing patterns in the lizard, Sceloporus virgatus. Amphibia-Reptilia 20:185-194. Abts, M. L. 1987. Environment and variation in life history traits of the Chuckwalla, Sauromalus obesus. Ecological Monographs 57:215-232. Achaval, F., and A. Olmos. 2003. Anfibios y reptiles del Uruguay. Montevideo, Uruguay: Facultad de Ciencias. Achaval, F., and A. Olmos. 2007. Anfibio y reptiles del Uruguay, 3rd edn. Montevideo, Uruguay: Serie Fauna 1. Ackermann, T. 2006. Schreibers Glatkopfleguan Leiocephalus schreibersii. Munich, Germany: Natur und Tier. Ackley, J. W., P. J. Muelleman, R. E. Carter, R. W. Henderson, and R. Powell. 2009. A rapid assessment of herpetofaunal diversity in variously altered habitats on Dominica. -
Bulletin 67 & 68 Lizards of VA
VIRGINIA HEnPnrnOGICAL SOCIETY SPECIAL IIULLETUY ” ® ( ? "A" SCALE TYPES: SMOOTH (L) SPINY (C) GRANULAR (R) HEAD PLATES OF THE SKINKS (Eumeces) VIRGINIA HERPETOLOGICAL SOCIETY BULLETIN No. 67 DESCRIPTION OF THE LIZARDS OF VIRGINIA Identification of the lizards de following pages include a specially- pends, prim arily, upon the sca les on prepared "key to the lizards of Vir the side and top o f the head, and be gin ia " and diagrams recommended fo r neath the tail, as veil as the color. use with that "key" by its author. It w ill be necessary to have, or to It is hoped that the total assembled gain, some familiarity with the large VHS sp ecia l b u lletin (VHS-B Nos. 67 scales or plates on the head and the and 68) w ill a s s is t you in making an belly, as well as the overall appear accurate identification in the field. ance of the collected specimens. The Locality records are badly needed. STANDARD COMMON NAMES (l.) Green Anole (2.) Six-lined Racerunner (3») Northern Coal Skink (4.) Five-lined Skink • (5 .) Southeastern Five-lined Skink (6.) Broad-headed Skink ( 7 •) Ground Skink (8.) Eastern Slender Glass Lizard ( 9») Eastern Glass Lizard ' ' ( 10.) Northern Fence Lizard SCIENTIFIC NAMES FOR VA. LIZARDS 1. Anolis c_. carolinens is 2* Cnemidophorus s . sexlineatus 3. Eumeces a. anthracinus 4. Eumeces fasciatu s • 5. Eumeces inexpectatus 6. Eumeces la ticep s 7. Lygosoma la tera le 8. Ophisaurus attenuatus longicaudus 9. Ophisaurus ventralis 10. Sceloporus undulatus hyacinthinus - 1 - 2 VHS BULLETIN No. -
Summer Movements of the Common Five-Lined Skink (Plestiodon Fasciatus) in the Northern Portion of Its Range
Herpetological Conservation and Biology 13(3):743–752. Submitted: 3 July 2018; Accepted: 25 November 2018; Published: 16 December 2018. SUMMER MOVEMENTS OF THE COMMON FIVE-LINED SKINK (PLESTIODON FASCIATUS) IN THE NORTHERN PORTION OF ITS RANGE DANIEL J. BRAZEAU1 AND STEPHEN J. HECNAR1,2 1Department of Biology, Lakehead University, 955 Oliver Road, Thunder Bay, Ontario, P7B 5E1, Canada 2Corresponding author, e-mail: [email protected] Abstract.—Common Five-lined Skinks (Plestiodon [formerly Eumeces] fasciatus) are difficult to study due to their small size, secretive habits, and semi-fossorial natural history. Habitat selection and dispersal have been studied at several locations across the range of the species, but few details of movements are known. Our objectives were to use radio-telemetry to gain more insight into skink movements and to test the efficacy of small, lightweight transmitters that we externally attached. We fitted 31 skinks with transmitters that provided up to 16 consecutive days of dispersal information. Movements varied greatly among individuals with some staying close to initial capture sites while most moved tens to hundreds of meters over a short period of observation. We located most of the tracked individuals under cover of woody debris but found they were much more mobile than previous mark- recapture studies suggested. Our tracking supported the idea that traditional home ranges were not occupied, but instead most individuals made regular linear movements while returning to the same locations occasionally. Individuals spent on average just over 30% of their time underground, in grass tussocks, and inside standing trees near the end of the active season. -
Lizard ID Guide
Lizards of Anderson County, TN Lizards are extraordinary gifts of nature. World-wide there are close to 6,000 species. The United States is home to more than100 native species, along with many exotic species that have become established, especially in Florida. Tennessee has 9 species, 6 of which are listed for Anderson County. Some are fairly widespread and easy to observe, such as the Common Five-lined Skink below. Unfortunately, the liberal use of pesticides, combined with predation by free roaming house cats have taken a heavy toll on our lizard populations. Most lizards are insect eating machines and their ecological services should be promoted through backyard and schoolyard wildlife habitat projects. Lizard watching is great fun, and over time, observers can gain interesting insights into lizard behavior. Your backyard may be a good place to start your lizarding career. This guide will be helpful for identifying our local lizards and will also provide you with examples of lizard behaviors to observe. Some species must be captured—this can be challenging—to insure accurate identification. Please see the back page for more resources. Lizarding Lizard watching, often referred to as lizarding, will likely never be as popular as bird watching (birding), but there is an advantage to being a “lizarder.” Unlike birders, you don’t need to be an early riser. Bright sunny days with warm temperatures are the keys for successful lizarding, but like birding, close-up binoculars are helpful. A lizard’s life centers around three performance activities: 1) avoiding predators, 2) feeding, and 3) reproduction. Lizard performance is all about optimal body temperature. -
Jnah Issn 2333-0694
ISSN 2333-0694 JNAHThe Journal of North American Herpetology Volume 2020, Number 1 2 July 2020 journals.ku.edu/jnah DO LATITUDE, ELEVATION, TEMPERATURE, AND PRECIPITATION INFLUENCE BODY AND CLUTCH SIZES OF FEMALE COMMON FIVE-LINED SKINKS, PLESTIODON FASCIATUS (LINNAEUS, 1758)? JAKE S. MORRISSEY1, BRANDON BARR1, ANDREW E. AUSTIN1, LAUREN R. BABCOCK1, AND ROBERT POWELL1,2 1Department of Biology, Avila University, Kansas City, Missouri 64145, USA 2Corresponding author. E-mail: [email protected] ABSTRACT: Common Five-lined Skinks (Plestiodon fasciatus) have an extensive distribution that in- cludes much of eastern North America. We examined 490 female specimens (274 with putative clutch sizes) from throughout the range to see if latitude, elevation, mean annual temperature, and/or mean annual precipitation affected body or clutch sizes. We predicted that larger females would produce larger clutches, latitude and elevation would negatively affect both body and clutch sizes, and that temperature and precipitation would exert a positive effect. Our results did not consistently support those predictions. Body size was positively associated with latitude, negatively associated with tem- perature, and not associated with elevation or precipitation. Clutch size was not related to female body size, but in most instances was positively associated with temperature and precipitation but negatively associated with elevation and latitude. EffectivelyK -selected in the North and r-selected in the South, body and clutch sizes in this species appear to be responding to different selective pressures. We eval- uated probable causes for the opposite trends in these two life-history traits. Key Words: Bergmann’s rule; r- and K-selection; Resource rule; Temperature-size rule. -
Response of Reptile and Amphibian Communities to the Reintroduction of Fire T in an Oak/Hickory Forest ⁎ Steven J
Forest Ecology and Management 428 (2018) 1–13 Contents lists available at ScienceDirect Forest Ecology and Management journal homepage: www.elsevier.com/locate/foreco Response of reptile and amphibian communities to the reintroduction of fire T in an oak/hickory forest ⁎ Steven J. Hromadaa, , Christopher A.F. Howeyb,c, Matthew B. Dickinsond, Roger W. Perrye, Willem M. Roosenburgc, C.M. Giengera a Department of Biology and Center of Excellence for Field Biology, Austin Peay State University, Clarksville, TN 37040, United States b Biology Department, University of Scranton, Scranton, PA 18510, United States c Ohio Center for Ecology and Evolutionary Studies, Department of Biological Sciences, Ohio University, Athens, OH 45701, United States d Northern Research Station, U.S. Forest Service, Delaware, OH 43015, United States e Southern Research Station, U.S. Forest Service, Hot Springs, AR 71902, United States ABSTRACT Fire can have diverse effects on ecosystems, including direct effects through injury and mortality and indirect effects through changes to available resources within the environment. Changes in vegetation structure suchasa decrease in canopy cover or an increase in herbaceous cover from prescribed fire can increase availability of preferred microhabitats for some species while simultaneously reducing preferred conditions for others. We examined the responses of herpetofaunal communities to prescribed fires in an oak/hickory forest in western Kentucky. Prescribed fires were applied twice to a 1000-ha area one and four years prior to sampling, causing changes in vegetation structure. Herpetofaunal communities were sampled using drift fences, and vegetation attributes were sampled via transects in four burned and four unburned plots. Differences in reptile community structure correlated with variation in vegetation structure largely created by fires. -
Ctenosaura Similis) on the on 5 May 2013 at 1406 H, We Observed an Adult Female Southwestern Coast of Florida
WWW.IRCF.ORG/REPTILESANDAMPHIBIANSJOURNALTABLE OF CONTENTS IRCF REPTILES & AMPHIBIANSIRCF REPTILES • VOL15, N&O AMPHIBIANS4 • DEC 2008 189 • 21(2):69–70 • JUN 2014 IRCF REPTILES & AMPHIBIANS CONSERVATION AND NATURAL HISTORY TABLE OF CONTENTS FEATURE ARTICLES The . NonnativeChasing Bullsnakes (Pituophis catenifer sayi ) inBlack Wisconsin: Spiny-tailed Iguana, On the Road to Understanding the Ecology and Conservation of the Midwest’s Giant Serpent ...................... Joshua M. Kapfer 190 . The Shared History of Treeboas (Corallus grenadensis) and Humans on Grenada: CtenosauraA Hypothetical Excursion ............................................................................................................................similis Gray 1831 (Squamata:Robert W. Henderson 198 RESEARCHIguanidae), ARTICLES Preying upon the . The Texas Horned Lizard in Central and Western Texas ....................... Emily Henry, Jason Brewer, Krista Mougey, and Gad Perry 204 . The Knight Anole (Anolis equestris) in Florida Native ............................................. SoutheasternBrian J. Camposano, Kenneth L. Krysko, Kevin Five-lined M. Enge, Ellen M. Donlan, and Michael GranatoskySkink, 212 CONSERVATION ALERT Plestiodon. World’s Mammals in Crisis ............................................................................................................................................................. inexpectatus Taylor 1932 220 . More Than Mammals ..................................................................................................................................................................... -
1 Sequencing and Comparative Analysis of The
SEQUENCING AND COMPARATIVE ANALYSIS OF THE MITOCHONDRIAL CYTOCHROME B GENE IN THE MARION UPLANDS FLORIDA SAND SKINK (PLESTIODON REYNOLDSI) by Taylor Locklear A Senior Honors Project Presented to the Honors College East Carolina University In Partial Fulfillment of the Requirements for Graduation with Honors by Taylor Locklear Greenville, NC May 2016 Approved by: Trip Lamb Department of Biology, Thomas Harriot College of Arts and Sciences 1 Abstract The Florida sand skink (Plestiodon reynoldsi)—a small (~10 cm) lizard endemic to the peninsula—is a ‘sand-swimming’ specialist restricted to Florida scrub habitat on the state’s central highland ridges. Florida scrub has been severely fragmented through urban growth and citrus farming, and less than 10% of this ecosystem remains. Given the skink’s limited geographic range and extensive population fragmentation, P. reynoldsi was listed as a federally threatened species in 1987. I surveyed skink populations from the Marion Uplands, where suitable lizard habitat is naturally (and has been historically) isolated from scrub on nearby Mt. Dora and Lake Wales ridges. I wanted to determine genetic relatedness of Marion Uplands skinks to those inhabiting these two ridges and hypothesized that Marion populations should be more similar genetically to those on the Mt. Dora ridge, given their geographic proximity. Mitochondrial DNA sequence analysis confirmed this hypothesis but also revealed unexpectedly high levels of genetic divergence between the Marion and Mt. Dora populations. Indeed, observed genetic divergence was comparable to that detected between Marion and Lake Wales populations. 2 Acknowledgments I thank Paul Moler of the Florida Fish and Wildlife Commission for providing the tail tip samples utilized in this project. -
Inventory of Amphibians and Reptiles at Death Valley National Park
Inventory of Amphibians and Reptiles at Death Valley National Park Final Report Permit # DEVA-2003-SCI-0010 (amphibians) and DEVA-2002-SCI-0010 (reptiles) Accession # DEVA- 2493 (amphibians) and DEVA-2453 (reptiles) Trevor B. Persons and Erika M. Nowak Common Chuckwalla in Greenwater Canyon, Death Valley National Park (TBP photo). USGS Southwest Biological Science Center Colorado Plateau Research Station Box 5614, Northern Arizona University Flagstaff, Arizona 86011 May 2006 Death Valley Amphibians and Reptiles_____________________________________________________ ABSTRACT As part of the National Park Service Inventory and Monitoring Program in the Mojave Network, we conducted an inventory of amphibians and reptiles at Death Valley National Park in 2002- 2004. Objectives for this inventory were to: 1) Inventory and document the occurrence of reptile and amphibian species occurring at DEVA, primarily within priority sampling areas, with the goal of documenting at least 90% of the species present; 2) document (through collection or museum specimen and literature review) one voucher specimen for each species identified; 3) provide a GIS-referenced list of sensitive species that are federally or state listed, rare, or worthy of special consideration that occur within priority sampling locations; 4) describe park-wide distribution of federally- or state-listed, rare, or special concern species; 5) enter all species data into the National Park Service NPSpecies database; and 6) provide all deliverables as outlined in the Mojave Network Biological Inventory Study Plan. Methods included daytime and nighttime visual encounter surveys, road driving, and pitfall trapping. Survey effort was concentrated in predetermined priority sampling areas, as well as in areas with a high potential for detecting undocumented species.