Overland Movement by an Eastern Musk Turtle (Sternotherus Odoratus)

Total Page:16

File Type:pdf, Size:1020Kb

Overland Movement by an Eastern Musk Turtle (Sternotherus Odoratus) Herpetology Notes, volume 14: 775-776 (2021) (published online on 16 May 2021) Overland movement by an eastern musk turtle (Sternotherus odoratus) David C. Seburn1,* and Mackenzie Burns1 The eastern musk turtle (Sternotherus odoratus were approximately 280 m to the east of the turtle Latreille in Sonnini & Latreille, 1801) is a freshwater (Fig. 1). The intervening habitat between the turtle and turtle native to eastern North America that is rarely found the waterbodies was a mixture of old field and open far from water (Ernst and Lovich, 2009). In one radio- woods. tracking study, none of the 17 eastern musk turtles were It is uncertain why the eastern musk turtle was on found on land (Wilhelm and Plummer, 2012). Home the road. It could have been moving from the river to ranges of eastern musk turtles are typically confined to the wetland (or vice versa). Such an inter-waterbody one body of water (Ernst and Lovich, 2009). Eastern movement would be at least 460 m. The use of multiple musk turtles are commonly described as “a highly aquatic wetlands by eastern musk turtles has been reported, turtle that seldom wanders far from water” (Mitchell, but such wetlands are typically less than 100 m apart 1994). They experience high evaporative water loss (Attum et al., 2013). The seasonal drying of wetlands rates compared to many other turtle species (Ernst, can cause turtles to move to other wetlands, however, 1968; Murphy et al., 2016) and this likely explains at eastern musk turtles are more likely to remain in drying least part of the lack of terrestrial movements. Given wetlands than other turtle species (Gibbons et al., 1983) their highly aquatic nature, observations of eastern and the maximum observed terrestrial movement from musk turtles away from water are of interest to better a seasonal wetland was only 48.7 m (Buhlman and understand the spatial ecology of this species. Here we Gibbons, 2001). It is unknown if the wetland to the report an observation of an eastern musk turtle on land west was drying up in early June, however, the total away from any waterbody. precipitation was above average in April and May On 15 June 2018, while conducting a survey of (165.0 mm vs. 154.8 mm) at the Ottawa International turtle road mortality, we encountered a dead eastern Airport, 65 km away (Environment Canada, 2021). It musk turtle along a paved, two-lane road in Lanark County, Ontario, Canada. The location of the turtle (45.0342°N, -76.3895°W ± 6 m) was determined with a handheld Garmin eTrex GPS. The body of the turtle was in poor condition and could not be sexed, but it was approximately 9 cm plastron length indicating it was an adult (Ernst and Lovich, 2009). There were no waterbodies within view of the road, but subsequent mapping of the observation using QGIS version 3.4 (QGIS Development Team 2021) indicated the turtle was between two waterbodies. An approximately 3 ha wetland was roughly 180 m to the west of the turtle, while the Clyde River and associated riparian wetlands Figure 1. Location of eastern musk turtle (red point) found 1 Canadian Wildlife Federation, 350 Michael Cowpland Drive, dead on a road in Lanark County, Ontario, Canada, on 15 June Ottawa, Ontario K2M 2W1 Canada. 2018. Wetland edges highlighted in blue. The eastern musk * Corresponding author. E-mail: [email protected] turtle was ~180 m from the wetland to the west, and ~280 m to © 2021 by Herpetology Notes. Open Access by CC BY-NC-ND 4.0. the wetland and river to the east. 776 David C. Seburn & Mackenzie Burns seems unlikely that an eastern musk turtle from the river Buhlmann, K.A., Gibbons, J.W. (2001): Terrestrial habitat use would trek overland 460 m to a small wetland. A shorter by aquatic turtles from a seasonally fluctuating wetland: path would have been from the western branch of the implications for wetland conservation boundaries. Chelonian Conservation and Biology 4(1): 115–127. river and south to the wetland (Fig. 1). The shorter path Cagle, F.R. (1937): Egg laying habits of the slider turtle (Pseudemys would also have avoided a small hill between the road troostii), the painted turtle (Chrysemys picta), and the musk turtle and the small wetland. The habitat in the small wetland (Sternotherus odoratus). Journal of the Tennessee Academy of is also unlikely to have been superior to the diverse Science 12(1): 87–95. aquatic habitats available along the river. Clark, W.S. (1982): Turtles as a food source of nesting Bald Eagles The turtle could have been making a limited terrestrial in the Chesapeake Bay region. Journal of Field Ornithology movement from the wetland or the river. Such a 53(1): 49–51. Edmonds, J.H. (1998): Population ecology of the Stinkpot Turtle movement could have been for nesting purposes (if the (Stenotherus odoratus) in Georgian Bay, Ontario. Unpublished turtle was a gravid female), because the turtle was found MSc, University of Guelph, Guelph, Canada. in June, the typical nesting season for turtles in this area. Environment Canada (2021): Canadian Climate Normals 1981– While this is theoretically possible, eastern musk turtles 2010. Government of Canada. https://climate.weather.gc.ca/ typically nest within 20 m of water (Cagle, 1937; Ernst, climate_normals/results_1981_2010_e.html 1986; Edmonds, 1998) with a maximum known distance Ernst, C.H. (1968): Evaporative water-loss relationships of turtles. of 45 m from water (Ernst and Lovich, 2009). Journal of Herpetology 2(3/4): 159–161. Ernst, C.H. (1986): Ecology of the turtle, Sternotherus odoratus, We cannot rule out the possibility that the eastern musk in southeastern Pennsylvania. Journal of Herpetology 20(3): turtle did not get to the road on its own. Shells of eastern 341–352. musk turtles have been found in a number of Bald Eagle Ernst, C.H., Lovich, J.E. (2009): Turtles of the United States and (Haliaeetus lucocephalus) nests (Bendell, 1959; Clark, Canada. Second edition. Baltimore, Maryland, USA, Johns 1982), so it is possible that a predator dropped the Hopkins University Press. eastern musk turtle on the road or a scavenger left the Gibbons, J.W., Greene, J.L., Congdon, J.D. (1983): Drought-related dead turtle on the road. responses of aquatic turtle populations. Journal of Herpetology 17(3): 242–246. Eastern musk turtles have been documented to move Laverty, J.F., Korol, B., Litzgus, J.D. (2016): Measuring the effects more than 1.5 km along waterways (Laverty et al., of water-based recreation on the spatial ecology of Eastern Musk 2016), but overland movements appear to be quite rare. Turtles (Sternotherus odoratus) in a provincial park in Ontario, The longest documented overland movement we have Canada. Copeia 104(2): 440–447. found is an adult eastern musk turtle “found abroad in Mitchell, J.C. (1994): The Reptiles of Virginia. Washington, USA, a hardwood forest about 396 m from the nearest known Smithsonian Institution Press. body of water” in North Carolina (Palmer and Braswell, Murphy, C.M., Tuberville, T.D., Maerz, J.C., Andrews, K.M. (2016): Evaporative water loss rates of four species of aquatic 1995). Unfortunately, no other details are available on turtles from the Coastal Plain of the southeastern United States. this observation. It remains unclear why and how often Journal of Herpetology 50(3): 457–463. lengthy overland forays are made but we encourage Palmer, W.M., Braswell, A.L. (1995): Reptiles of North Carolina. researchers to report terrestrial observations away from Chapel Hill, North Carolina, USA, University of North Carolina water to better understand the spatial ecology of eastern Press. musk turtles. QGIS Development Team (2021): QGIS Geographic Information System, version 3.4. Open Source Geospatial Foundation Project. Acknowledgements. We acknowledge the support of the Wilhelm, C.E., Plummer, M.V. (2012): Diet of radiotracked Rogers Foundation for funding our turtle conservation work. Musk Turtles, Sternotherus odoratus, in a small urban stream. We are grateful to Damien Mullin for providing a difficult to Herpetological Conservation and Biology 7(2): 258–264. locate reference and to Jolene Laverty and Brian Butterfield for providing comments on the manuscript. References Attum, O., Cutshall, C.D., Eberly, K., Day, H., Tietjen, B. (2013): Is there really no place like home? Movement, site fidelity, and survival probability of translocated and resident turtles. Biodiversity and Conservation 22(13/14): 3185–3195. Bendell, J.F. (1959): Bony shells of musk turtles in nest of Bald Accepted by Eric Munscher Eagle. Canadian Field-Naturalist 73: 131–132..
Recommended publications
  • The Ecology and Evolutionary History of Two Musk Turtles in the Southeastern United States
    The University of Southern Mississippi The Aquila Digital Community Dissertations Spring 2020 The Ecology and Evolutionary History of Two Musk Turtles in the Southeastern United States Grover Brown Follow this and additional works at: https://aquila.usm.edu/dissertations Part of the Genetics Commons Recommended Citation Brown, Grover, "The Ecology and Evolutionary History of Two Musk Turtles in the Southeastern United States" (2020). Dissertations. 1762. https://aquila.usm.edu/dissertations/1762 This Dissertation is brought to you for free and open access by The Aquila Digital Community. It has been accepted for inclusion in Dissertations by an authorized administrator of The Aquila Digital Community. For more information, please contact [email protected]. THE ECOLOGY AND EVOLUTIONARY HISTORY OF TWO MUSK TURTLES IN THE SOUTHEASTERN UNITED STATES by Grover James Brown III A Dissertation Submitted to the Graduate School, the College of Arts and Sciences and the School of Biological, Environmental, and Earth Sciences at The University of Southern Mississippi in Partial Fulfillment of the Requirements for the Degree of Doctor of Philosophy Approved by: Brian R. Kreiser, Committee Co-Chair Carl P. Qualls, Committee Co-Chair Jacob F. Schaefer Micheal A. Davis Willian W. Selman II ____________________ ____________________ ____________________ Dr. Brian R. Kreiser Dr. Jacob Schaefer Dr. Karen S. Coats Committee Chair Director of School Dean of the Graduate School May 2020 COPYRIGHT BY Grover James Brown III 2020 Published by the Graduate School ABSTRACT Turtles are among one of the most imperiled vertebrate groups on the planet with more than half of all species worldwide listed as threatened, endangered or extinct by the International Union of the Conservation of Nature.
    [Show full text]
  • Diets of Freshwater Turtles Often Reflect the Availability of Food Resources in the Environment
    Herpetological Conservation and Biology 8(3):561−570. HerpetologicalSubmitted: 26 March Conservation 2013; Accepted: and Biology 21 October 2013; Published: 31 December 2013. RazoR-Backed Musk TuRTle (SternotheruS carinatuS) dieT acRoss a GRadienT of invasion carla l. atkinSon1,2, 3 1Oklahoma Biological Survey, 111 E. Chesapeake St., Norman, OK 73019 2Department of Biology and Ecology and Evolutionary Biology Graduate Program, University of Oklahoma, Norman, Ok 73019 3Present Address: Dept. of Ecology and Evolutionary Biology, Corson Hall, Cornell University, Ithaca, NY 14853 e-mail: [email protected] abstract.—diets of freshwater turtles often reflect the availability of food resources in the environment. accordingly, bottom- feeding turtles’ diets are typically composed of benthic macroinvertebrate fauna (e.g., insects and mollusks). However, the composition of benthic systems has changed because many freshwater ecosystems have been invaded by non-native species, including bivalve species such as the asian clam, corbicula fluminea. i studied the diet of Sternotherus carinatus, the Razor- backed Musk Turtle, in southeastern oklahoma across three zones of corbicula abundances: no corbicula, moderate corbicula densities, and high corbicula densities. i hypothesized that the composition of corbicula in the diet would increase with increased abundance of corbicula in the riverine environment. Turtles were caught by snorkel surveys in the little and Mountain fork rivers and kept overnight for the collection of fecal samples. The diet was similar to that found in previous studies on S. carinatus except that corbicula is a new component of the diet and composed the majority of the diet in high-density corbicula areas. an index of Relative importance (iRi) showed that corbicula was the most important prey item in the areas with high corbicula density, was equally as important as gastropods in the areas with moderate corbicula density, and was absent from the diet in areas without corbicula.
    [Show full text]
  • In AR, FL, GA, IA, KY, LA, MO, OH, OK, SC, TN, and TX): Species in Red = Depleted to the Point They May Warrant Federal Endangered Species Act Listing
    Southern and Midwestern Turtle Species Affected by Commercial Harvest (in AR, FL, GA, IA, KY, LA, MO, OH, OK, SC, TN, and TX): species in red = depleted to the point they may warrant federal Endangered Species Act listing Common snapping turtle (Chelydra serpentina) – AR, GA, IA, KY, MO, OH, OK, SC, TX Florida common snapping turtle (Chelydra serpentina osceola) - FL Southern painted turtle (Chrysemys dorsalis) – AR Western painted turtle (Chrysemys picta) – IA, MO, OH, OK Spotted turtle (Clemmys gutatta) - FL, GA, OH Florida chicken turtle (Deirochelys reticularia chrysea) – FL Western chicken turtle (Deirochelys reticularia miaria) – AR, FL, GA, KY, MO, OK, TN, TX Barbour’s map turtle (Graptemys barbouri) - FL, GA Cagle’s map turtle (Graptemys caglei) - TX Escambia map turtle (Graptemys ernsti) – FL Common map turtle (Graptemys geographica) – AR, GA, OH, OK Ouachita map turtle (Graptemys ouachitensis) – AR, GA, OH, OK, TX Sabine map turtle (Graptemys ouachitensis sabinensis) – TX False map turtle (Graptemys pseudogeographica) – MO, OK, TX Mississippi map turtle (Graptemys pseuogeographica kohnii) – AR, TX Alabama map turtle (Graptemys pulchra) – GA Texas map turtle (Graptemys versa) - TX Striped mud turtle (Kinosternon baurii) – FL, GA, SC Yellow mud turtle (Kinosternon flavescens) – OK, TX Common mud turtle (Kinosternon subrubrum) – AR, FL, GA, OK, TX Alligator snapping turtle (Macrochelys temminckii) – AR, FL, GA, LA, MO, TX Diamond-back terrapin (Malaclemys terrapin) – FL, GA, LA, SC, TX River cooter (Pseudemys concinna) – AR, FL,
    [Show full text]
  • Common Musk Turtle
    Common Musk Turtle Common Musk Turtle [Stinkpot] - Pl. 1 (Sternotherus odoratus) Identification: 2" - 5 3/8". The Common Musk Turtle has an olive-brown to black carapace, sometimes marked with dark spots or streaks. The carapace is smooth and domed, and may have green algae growing on its surface. The plastron is yellow to brown. Two key identifying features on the relatively small plastron are: (1) a single hinge, and (2) squarish pectoral scutes (just in front of the hinge). Other key features are two light stripes on the head (these may be hidden by dark pigment), and barbels (small fleshy projections) on the chin and throat. Where to find them: The Common Musk Turtle can be found in still or slow-moving bodies of water, where it prefers to walk slowly along the bottom. It basks just at or below the surface, but can also be seen basking on fallen trees and branches overhanging the water. When to find them: Active April through October. Range: Entire state. Note: In New Jersey, the turtle most similar to this is the Eastern Mud Turtle, which lacks the stripes and the barbels, and has two hinges instead of one. Common Musk Turtle (Sternotherus odoratus) - text pg. 10 Key Features - Carapace: smooth & domed. - Plastron: small with single hinge. - Barbels on chin, two light stripes on head. New Jersey Division of Fish and Wildlife ~ 2003 Excerpt from: Schwartz, V. & D. Golden, “Field Guide to Reptiles and Amphibians of New Jersey”. New Jersey Division of Fish and Wildlife 2002. Order the complete guide at - http://www.state.nj.us/dep/fgw/products.htm.
    [Show full text]
  • Species Assessment for Eastern Musk Turtle
    Species Status Assessment Class: Reptilia Family: Kinosternidae Scientific Name: Sternotherus odoratus Common Name: Eastern musk turtle (stinkpot) Species synopsis: Also known as the stinkpot, the eastern musk turtle emits a distinctive musky odor when threatened. It is highly aquatic, leaving the water infrequently, and moving awkwardly on land when it must. Occupied habitats include lakes, ponds, and rivers that have a muddy bottom substrate and little or no current. The musk turtle has a large distribution that extends across most of the eastern United States and into southern Canada, with a noticeable gap around higher elevation areas. New York is near the northern edge of the range. Musk turtles are common and apparently secure across the range with the exception of populations on the northern edge in Ontario and Quebec. Threats include shoreline development and the removal of submerged aquatic vegetation for recreational activities. I. Status a. Current and Legal Protected Status i. Federal ____Not Listed_______________________ Candidate? ___No_____ ii. New York ____SGCN_________________________________________________________ b. Natural Heritage Program Rank i. Global ____G5____________________________________________________________ ii. New York ____S5_____________________ Tracked by NYNHP? ___No____ Other Rank: IUCN – Least Concern COSEWIC – Special Concern Species of Low Priority (NEPARC 2010) 1 Status Discussion: Van Dijk (2011) refers to common musk turtle as a “very widespread, common, and adaptable species” that is “in no way threatened” despite some marginal populations of local conservation interest, including occurrences in Ontario and Quebec. Musk turtles are listed as Threatened in Canada where declines have been attributed to wetland destruction and shoreline alteration. It is also protected in Canada under the federal Species at Risk Act and is listed as a Specially Protected Reptile under the Ontario Fish and Wildlife Conservation Act.
    [Show full text]
  • Genus: Sternotherus (Musk Turtles) - Darrell Senneke Copyright © 2003 World Chelonian Trust
    Genus: Sternotherus (Musk Turtles) - Darrell Senneke Copyright © 2003 World Chelonian Trust. All rights reserved Sternotherus carinatus - Razor-backed Musk Turtle Sternotherus depressus - Flattened Musk Turtle Sternotherus minor - Loggerhead Musk Turtle Sternotherus minor peltifer - Stripe-neck Musk Turtle Sternotherus odoratus - Common Musk Turtle This care sheet is intended only to cover the general care of these species. Further research to best develop a maintenance plan for whichever species you are caring for is essential.. Many taxonomists often combine genus Sternotherus with Kinosternon as sub- genera of the Family Kinosternidae. While these animals share many of the same habitats, features and care requirements, for the purpose of this care sheet they will be treated as a full Genus. Musk turtles can be found from the Canadian Southern border to Florida and West to the Rocky Mountains. These species are more carnivorous than most turtles with a natural diet that relies heavily on fish, snails, crustaceans and insects. While the Razor-back Musk turtle can attain a size of 15 cm. (6 inches), the much more commonly seen Stinkpot only attains 8 - 10 cm (3 - 4 inches) maximum. Present knowledge and technology make Musk turtles easily maintained animals as long as a person is willing to provide some basic requirements. Thanks to the success that breeders are having with these species it is now possible to purchase many of these species as hatchlings from captive born stock. Some of the species are threatened or endangered in nature, do not remove these animals from the wild. HOUSING MUSK TURTLES INDOORS - The most useful form of indoor accommodation for Sternotherus consists of an aquarium.
    [Show full text]
  • Kinosternon Subrubrum (Bonnaterre 1789) – Eastern Mud Turtle
    Conservation Biology of Freshwater Turtles and Tortoises: A Compilation ProjectKinosternidae of the IUCN SSC — KinosternonTortoise and Freshwater subrubrum Turtle Specialist Group 101.1 A.G.J. Rhodin, J.B. Iverson, P.P. van Dijk, K.A. Buhlmann, P.C.H. Pritchard, and R.A. Mittermeier, Eds. Chelonian Research Monographs (ISSN 1088-7105) No. 5, doi:10.3854/crm.5.101.subrubrum.v1.2017 © 2017 by Chelonian Research Foundation and Turtle Conservancy • Published 17 September 2017 Kinosternon subrubrum (Bonnaterre 1789) – Eastern Mud Turtle WALTER E. MESHAKA, JR.1, J. WHITFIELD GIBBONS2, DANIEL F. HUGHES3, MICHAEL W. KLEMENS4, AND JOHN B. IVERSON5 1State Museum of Pennsylvania, 300 North Street, Harrisburg, Pennsylvania 17120 USA [[email protected]]; 2Savannah River Ecology Lab, Drawer E, Aiken, South Carolina 29802 USA [[email protected]]; 3University of Texas at El Paso, El Paso, Texas 79968 USA [[email protected]]; 4Department of Herpetology, American Museum of Natural History, Central Park West at 79th Street, New York, New York 10024 USA [[email protected]]; 5Department of Biology, Earlham College, Richmond, Indiana 47374 USA [[email protected]] SUMMARY. — The Eastern Mud Turtle, Kinosternon subrubrum (Family Kinosternidae), is a small (carapace length 85 to 120 mm) polytypic species of the eastern and central United States. All three historically recognized subspecies (K. s. subrubrum, K. s. steindachneri, and K. s. hippocrepis) are semi-aquatic turtles that inhabit much of the U.S. Atlantic and Gulf Coastal Plains. The Florida taxon (K. s. steindachneri) appears to represent a distinct species, but we continue to treat it as a subspecies for the purposes of this account.
    [Show full text]
  • Taxonomy and Phylogeny of the Higher Categories of Cryptodiran Turtles Based on a Cladistic Analysis of Chromosomal Data
    Copein, 1983(4), pp. 918-932 Taxonomy and Phylogeny of the Higher Categories of Cryptodiran Turtles Based on a Cladistic Analysis of Chromosomal Data John W. Bickham and John L. Carr Karyological data are available for 55% of all cryptodiran turtle species including members of all but one family. Cladistic analysis of these data, as well as con sideration of other taxonomic studies, lead us to propose a formal classification and phylogeny not greatly different from that suggested by other workers. We recognize 11 families and three superfamilies. The platysternid and staurotypid turtles are recognized at the familial level. Patterns and models of karyotypic evolution in turtles are reviewed and discussed. OVER the past 10 years knowledge of turtle and the relationship between the shell and pel karyology has grown to such an extent vic girdle. In the cryptodires ("hidden-necked" that the order Testudines is one of the better turtles), the neck is withdrawn into the body in known groups of lower vertebrates (Bickham, a vertical plane and the pelvis is not fused to 1983). Nondifferentially stained karyotypes are either the plastron or carapace, whereas in the known for 55% of cryptodiran turtle species pleurodires ("side-necked" turtles) the pelvic and banded karyotypes for approximately 25% girdle is fused to both the plastron and carapace (Bickham, 1981). From this body of knowledge, and the neck is folded back against the body in as well as a consideration of the morphological a horizontal plane. Cope's suborder Athecae variation in the order, we herein present a gen includes only the Dermochelyidae and is no eral review of the cryptodiran karyological lit longer recognized.
    [Show full text]
  • Sternotherus Odoratus (Latreille) Edgren (1960A), Albrecht (1967), Haines (1969), Zug (1971A)
    287.1 REPTILIA: TESTUDINES: KINOSTERNIDAE STERNOTHERUSODORATUS Catalogue of American Amphibians and Reptiles. of tuberculate scales on the inner surface of each crus and thigh, extensive exposed skin between the interplastral seams, and the REYNOLDS,SAMUELL. ANDSEIDEL, MICHAELE. 1982. Ster• anal vent extended beyond the posterior edge of the carapace. notherus odoratus. • DESCRIPTIONS. General descriptions: Carr (1952), Ernst and Barbour (1972), Conant (1975). Osteology: Williams (1950), Sternotherus odoratus (Latreille) Edgren (1960a), Albrecht (1967), Haines (1969), Zug (1971a). Stinkpot Shell: Adler (1960), Shah (1960), Tinkle (1962). Myology: Poglay• en-Neuwall (1953), Shah (1962), Schumacher (1973). Urogenital Testudo odorata Latreille, in Sonnini and Latreille, 1802:122. system: Risley (1933), Fox (1977). Sexual dimorphism: Risley Type-locality, "les eaux dorm antes de la Caroline"; restrict• (1930). Egg: Thing (1918), Edgren (1949), Ewert (1979). Cranial ed to "vicinity of Charleston [Charleston County], South arteries: McDowell (1961), Albrecht (1967). Penial morphology: Carolina" by Schmidt (1953:87). Type specimen undesignat• Zug (1966). Coelomic epithelium: Risley (1934). Pharynx: Sieben• ed. rock (1899). Choanal structure: Parsons and Stephens (1968). Ear: Testudo glutinata Daudin, 1802:194. Type-locality, "Etats-Unis Baird (1970). Retina: Ernst et a!. (1970). Cloacal bursa: Smith and d' Amerique"; restricted to "vicinity of Lancaster [Lancaster James (1958). Glands: Hebard and Charipper (1955), Cowan County], Pennsylvania" by Schmidt (1953:87). Type speci• (1973), Ehrenfeld and Ehrenfeld (1973), Winokur and Legler men deposited in the Mus. Natur. Hist. Nat. Paris (not ex• (1974), Manton (1979). amined by authors). Emys odorata: Schweigger, 1812:313. • ILLUSTRATIONS.Color or black and white photographs of Emys glutinata: Merrem, 1820:24. adults or hatchlings are in Ernst and Barbour (1972), Conant Terrapene boscii Merrem, 1820:27.
    [Show full text]
  • J"::X),, 200 400 Soo KM
    397.1 REPTILIA: TESTUDINES: KINOSTERNIDAE STERNOTHERUS Catalogue of American Amphibians and Reptiles. ZUG,GEORGER. 1986. Sternotherus. Sternotherus Gray Musk turtles Sternotherus Gray, 1825:211. Type species, S. odoratus by sub• sequent designation (Stejneger, 1902:236) . Sternothaerus Bell, 1825:305. Type species, S. odoratus by sub• .-.'-I sequent designation (Stejneger, 1902:236). I Sternoteirus Gravenhorst, 1829:17. Type species, none given; ap• I parently an orthographic emendation. I I Sternotheros Gray, 1831:13. A lapsus calami in the synonymy of -.ir:-··.t'·:~·-·7 Emys odoratum. I •• Armochelys Gray, 1855:46. Type species, A. odoratum by sub• sequent designation (Stejneger, 1902:237). Goniochelys Agassiz, 1857:423. Type species, G. triquetra (=S. carinatus) by subsequent designation (Zug, 1971 :448). j"::X),, 200 400 sOO KM. j'" t.("_. ~ ) .. Ozotheca Agassiz, 1857:424. Type species, O. odorata and O. tristycha (=S. odoratus) thus S. odoratus by monotypy. MAP. Present distribution of the genus Sternotherus. • CONTENT.Four species are currently recognized: Sternothe• rus carinatus, S. depressus, S. minor, and S. odoratus. ern Florida. This large range is occupied by a single species Ster• • DEFINITION.Sternotherus are small turtles; adults range in notherus odoratus. A single Mexican record (Chihuahua, Rio Sauz) carapace length from 75-160 mm. There is no apparent sexual of S. odoratus, although unconfirmed, may be valid (Conant and dimorphism in shell size, although the largest individuals are com• Berry, 1978; Smith and Smith, 1980). The remaining three monly females. The carapace outline is oblong or ovate in adults; species-the S. carinatus complex-are largely confined to the height of shell is species-specific from flattened to strongly peaked.
    [Show full text]
  • The Diet of the Eastern Musk Turtle (Sternotherus Odoratus) As It Pertains to Invasive Snail Consumption in a Freshwater Spring Habitat in Texas
    Herpetology Notes, volume 12: 1133-1139 (2019) (published online on 04 November 2019) The diet of the Eastern Musk Turtle (Sternotherus odoratus) as it pertains to invasive snail consumption in a freshwater spring habitat in Texas Madeleine Morrison1,2,*, Brian P. Butterfield3, Stephen G. Ross4, Chris Collins5, Andrew Walde1, Jordan Gray1, J. Brian Hauge6, and Eric C. Munscher1,7 Abstract. In this study we investigated the diet of the Eastern Musk Turtle (Sternotherus odoratus) in Comal Springs, a spring-fed lake system located in the Texas Hill Country. Due to high numbers of invasive snails in this system, we focused on consumption of invasive snails. The most abundant taxa present in the faecal samples were gastropods. In particular, three species of invasive snails, the Red-rimmed Melania (Melanoides tuberculata), the Quilted Melania (Tarebia granifera), and the Giant Ramshorn Snail (Marisa cornuarietis) were the most abundant items identified. We found fragments of M. tuberculata shells in the majority of the samples (77% male samples; 80% female samples; 78% total), opercula from M. cornuarietis in a smaller number of samples (20% male samples; 10% female samples; 16% total samples), and fragments of T. granifera shells in half of the faecal samples (50% male samples; 50% female samples; 50% total). No sexual difference in diet was apparent. Total consumption of molluscs was high relative to most other reports of S. odoratus diet. Our results suggest that the diet of S. odoratus in Comal Springs may have shifted towards focusing on the invasive snails as the result of a probable three-decade presence of these invasive species.
    [Show full text]
  • Journal of Vertebrate Paleontology Supplementary
    JOURNAL OF VERTEBRATE PALEONTOLOGY SUPPLEMENTARY DATA Fossil musk turtles (Kinosternidae, Sternotherus) from the late Miocene–early Pliocene (Hemphillian) of Tennessee and Florida JASON R. BOURQUE*, 1 and BLAINE W. SCHUBERT2 1Division of Vertebrate Paleontology, Florida Museum of Natural History, University of Florida, Gainesville, Florida 32611, U.S.A., [email protected]; 2Don Sundquist Center of Excellence in Paleontology and Department of Geosciences, East Tennessee State University, Johnson City, Tennessee 37614, U.S.A., [email protected] *Corresponding author TABLES TABLE S1. Updated vertebrate fauna from the Gray Fossil Site. Compiled from Wallace and Wang (2004), Bentley et al. (2008), Hulbert et al. (2009), Boardman and Schubert (2011), Schubert and Mead (2011), Mead et al. (2012). Additional unpublished identifications by S. C. Wallace, J. I. Mead, B.W.S., and J.R.B.. Osteichthyes Centrarchidae Amphibia Anura Ranidae Rana sp. Bufonidae Hylidae Caudata Ambystomatidae Ambystoma sp. Plethodontidae Plethodon sp. Desmognathus sp. Salamandridae Notophthalmus sp. Reptilia Testudines Chelydridae Chelydra sp. Kinosternidae Sternotherus palaeodorus, n. sp. Emydidae Chrysemys sp. Trachemys sp. aff. Emydoidea or Emys sp. Terrapene sp. Testudinidae Hesperotestudo sp. Crocodylia Alligatoridae Alligator sp. Squamata Anguidae Ophisaurinae Scincidae Helodermatidae TABLE 1S. (Continued) Heloderma sp. Colubridae Natricinae Colubrinae Viperidae Aves Anatidae Aix sp. Anas spp. Odontophoridae Rallidae Scolopacidae Scolopax sp. Tytonidae Mammalia Xenarthra Megalonychidae Insectivora Soricidae minimum 3 spp. present Talpidae minimum 2 spp. present Chiroptera Lagomorpha Leporidae Rodentia minimum 6 spp. present Proboscidea Gomphotheriidae Perissodactyla Equidae Cormohipparion emsliei Tapiridae Tapirus polkensis Rhinocerotidae Teleoceras sp. Artiodactyla Tayassuidae Prosthennops sp. sp. indet. Camelidae cf. Megatylopus sp. Carnivora TABLE S1. (Continued) Felidae cf. Machairodus sp.
    [Show full text]