DOCSLIB.ORG

Checklist Reptile and Amphibian

Total Page：16

File Type：pdf, Size：1020Kb

Download full-text PDF Read full-text
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 (Notophthalmus viridescens viridescens) (Lampropeltis getula getula) ☐ Eastern Mud Turtle ☐ Scarlet Kingsnake1 Toads (Kinosternon subrubrum) (Lampropeltis elapsoides) ☐ American Toad ☐ Eastern Musk Turtle ☐ Red-bellied Water Snake2 (Bufo (Anaxyrus) americanus) (Sternotherus odoratus) (Nerodia erythrogaster) ☐ Fowler’s Toad (Bufo (Anaxyrus) fowleri) Softshell Turtles ☐ Northern Water Snake (Nerodia sipedon) Tree Frogs ☐ Gulf Coast Spiny Softshell1 ☐ Brown Water Snake (Nerodia taxispilota) ☐ Northern Cricket Frog (Acris crepitans) (Apalone spinifera aspera) ☐ Rough Green Snake (Opheodrys aestivus) ☐ Cope’s Gray Treefrog (Hyla chrysoscelis) Alligators ☐ Queen Snake (Regina septemvittata) ☐ Green Treefrog5 (Hyla cinerea) ☐ Brown Snake (Storeria dekayi) ☐ American Alligator3, 6 ☐ Squirrel Treefrog5 (Hyla squirella) ☐ Red-bellied Snake (Alligator mississippiensis) ☐ Spring Peeper (Pseudacris crucifer) (Storeria occipitomaculata) ☐ Upland Chorus Frog (Pseudacris feriarum) Anoles ☐ Southeastern Crowned Snake Narrowmouth Toads ☐ Green Anole (Anolis carolinensis) (Tantilla coronata) ☐ Eastern Ribbon Snake ☐ Eastern Narrowmouth Toad Spiny Lizards (Thamnophis sauritus) (Gastrophryne carolinensis) ☐ Eastern Fence Lizard ☐ Eastern Garter Snake (Sceloporus undulatus) American Spadefoot Toads (Thamnophis sirtalis) ☐ Eastern Spadefoot (Scaphiopus holbrookii) Skinks ☐ Rough Earth Snake (Virginia striatula) 1 True Frogs ☐ Common Five-lined Skink ☐ Smooth Earth Snake (Virginia valeriae) (Plestiodon fasciatus) ☐ Bullfrog Venomous Snakes ☐ Southeastern Five-lined Skink (Rana (Lithobates) catesbeiana ☐ Copperhead (Agkistrodon contortrix) (Plestiodon inexpectatus) (catesbeianus)) ☐ Timber Rattlesnake4 ☐ Broad-headed Skink ☐ Green Frog (Rana (Lithobates) clamitans) (Crotalus horridus) (Plestiodon laticeps) 1NC Watch List, 2Historic or obscure record, 3Not native, 4NC Species of Special Concern, 5Recently established, 6Does not breed in region Taxonomic nomenclature follows: Amphibians and Reptiles of North Carolina Version 2. Checklist Publication Series: No. 04 © 2018 Mecklenburg County — All Rights Reserved. Photo: Bullfrog © Leigh Anne Carter..
Load more

Recommended publications
  • Xenosaurus Tzacualtipantecus. the Zacualtipán Knob-Scaled Lizard Is Endemic to the Sierra Madre Oriental of Eastern Mexico
    Xenosaurus tzacualtipantecus. The Zacualtipán knob-scaled lizard is endemic to the Sierra Madre Oriental of eastern Mexico. This medium-large lizard (female holotype measures 188 mm in total length) is known only from the vicinity of the type locality in eastern Hidalgo, at an elevation of 1,900 m in pine-oak forest, and a nearby locality at 2,000 m in northern Veracruz (Woolrich- Piña and Smith 2012). Xenosaurus tzacualtipantecus is thought to belong to the northern clade of the genus, which also contains X. newmanorum and X. platyceps (Bhullar 2011). As with its congeners, X. tzacualtipantecus is an inhabitant of crevices in limestone rocks. This species consumes beetles and lepidopteran larvae and gives birth to living young. The habitat of this lizard in the vicinity of the type locality is being deforested, and people in nearby towns have created an open garbage dump in this area. We determined its EVS as 17, in the middle of the high vulnerability category (see text for explanation), and its status by the IUCN and SEMAR- NAT presently are undetermined. This newly described endemic species is one of nine known species in the monogeneric family Xenosauridae, which is endemic to northern Mesoamerica (Mexico from Tamaulipas to Chiapas and into the montane portions of Alta Verapaz, Guatemala). All but one of these nine species is endemic to Mexico. Photo by Christian Berriozabal-Islas. amphibian-reptile-conservation.org 01 June 2013 | Volume 7 | Number 1 | e61 Copyright: © 2013 Wilson et al. This is an open-access article distributed under the terms of the Creative Com- mons Attribution–NonCommercial–NoDerivs 3.0 Unported License, which permits unrestricted use for non-com- Amphibian & Reptile Conservation 7(1): 1–47.
    [Show full text]
  • Queen Snake, Regina Septemvittata
    Queen Snake, Regina septemvittata Status: State: Endangered Federal: Not listed Identification This slender snake can reach lengths of 16-24 in. (41-61 cm) when fully grown. The dorsal (or upper) surface of a queen snake is a solid, grayish-brown color. A yellow band is present on the lower half of the body and extends from the snake’s chin to its tail. The belly of the snake is a white to yellow color with four characteristic stripes that make for easy identification. Of these four stripes, the two outer stripes are visibly thicker than the inner pair. Queen snakes have keeled scales and an © Rudolf G. Arndt anal plate that is divided. Habitat This species is highly aquatic and a very adept swimmer. Authorities report that swiftly flowing creeks, brooks and streams are the preferred habitat for queen snakes (Wright and Wright 1957). But finding them along the edges of more slowly flowing rivers and streams, and sometimes lakes, is not uncommon in some states. The queen snake’s diet (see below) always keeps it close to water, where it can sometimes be seen with just its head above the surface of the water. On occasion, a lucky observer might find these snakes basking in high numbers along the banks of streams and even hanging from streamside vegetation (Golden, personal observation). Such aggregations are probably unlikely in New Jersey, however. The best strategy for finding this species in the state would be to look under flat rocks and other debris along the banks of the Delaware River and its tributaries.
    [Show full text]
  • 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.
    [Show full text]
  • Veterans Park Herpetological Report Manning 2015
    To Whom It May Concern, The information in this document is the summary of a series of volunteer reptile and amphibian observations conducted in Hamilton Veteran’s Park in Mercer County, NJ. The document has been prepared for the Township of Hamilton. The results presented are from field observations and data collected in 2012, 2013, 2014, and 2015. The data from the first three years was taken informally during morning and evening walks with family. The data from 2015 was taken for a volunteer reptile and amphibian survey performed upon the request of the Township of Hamilton, Mercer County, NJ. This information is presented voluntarily for use in conservation endeavors. General Profile: Hamilton Veteran’s Park is a 350‐acre park managed by the Township of Hamilton in Mercer County, New Jersey. The park features a diversity of habitats within its boundaries, including a field which was the site of a former farm, a wetlands meadow, a smaller upland meadow, several patches of deciduous forest, a man‐made lake, temporary and permanent wetlands, an intermittent stream, and several permanent streams. The park is located on the physiographic province known as the inner coastal plain. Comments on General Fauna: The Veteran’s Park property provides a variety of habitats for native fauna to flourish. Healthy numbers of invertebrates have been observed during the survey. Checking under logs and other cover debris reveals a multitude of native decomposers, such as ants, earthworms, slugs, centipedes, harvestmen, and others. Ticks are occasionally seen in the fields, however most of those observed were dog ticks.
    [Show full text]
  • Mitochondrial Discordance and Gene Flow in a Recent Radiation of Toads
    Molecular Phylogenetics and Evolution 59 (2011) 66–80 Contents lists available at ScienceDirect Molecular Phylogenetics and Evolution journal homepage: www.elsevier.com/locate/ympev Nuclear–mitochondrial discordance and gene flow in a recent radiation of toads ⇑ Brian E. Fontenot , Robert Makowsky 1, Paul T. Chippindale Department of Biology, University of Texas at Arlington, Arlington, TX 76019, United States article info abstract Article history: Natural hybridization among recently diverged species has traditionally been viewed as a homogenizing Received 28 April 2010 force, but recent research has revealed a possible role for interspecific gene flow in facilitating species Revised 12 December 2010 radiations. Natural hybridization can actually contribute to radiations by introducing novel genes or Accepted 23 December 2010 reshuffling existing genetic variation among diverging species. Species that have been affected by natural Available online 19 January 2011 hybridization often demonstrate patterns of discordance between phylogenies generated using nuclear and mitochondrial markers. We used Amplified Fragment Length Polymorphism (AFLP) data in conjunc- Keywords: tion with mitochondrial DNA in order to examine patterns of gene flow and nuclear–mitochondrial dis- Toads cordance in the Anaxyrus americanus group, a recent radiation of North American toads. We found high Hybridization Gene flow levels of gene flow between putative species, particularly in species pairs sharing similar male advertise- Speciation ment calls that occur in close geographic proximity, suggesting that prezygotic reproductive isolating AFLPs mechanisms and isolation by distance are the primary determinants of gene flow and genetic differenti- Nuclear–mitochondrial discordance ation among these species. Additionally, phylogenies generated using AFLP and mitochondrial data were markedly discordant, likely due to recent and/or ongoing natural hybridization events between sympatric populations.
    [Show full text]
  • Distribution of the Queen Snake (Regina Septemvittata) in Arkansas Johnathan W
    Journal of the Arkansas Academy of Science Volume 61 Article 17 2007 Distribution of the Queen Snake (Regina septemvittata) in Arkansas Johnathan W. Stanley Arkansas State University, [email protected] Stanley E. Trauth Arkansas State University Follow this and additional works at: http://scholarworks.uark.edu/jaas Part of the Zoology Commons Recommended Citation Stanley, Johnathan W. and Trauth, Stanley E. (2007) "Distribution of the Queen Snake (Regina septemvittata) in Arkansas," Journal of the Arkansas Academy of Science: Vol. 61 , Article 17. Available at: http://scholarworks.uark.edu/jaas/vol61/iss1/17 This article is available for use under the Creative Commons license: Attribution-NoDerivatives 4.0 International (CC BY-ND 4.0). Users are able to read, download, copy, print, distribute, search, link to the full texts of these articles, or use them for any other lawful purpose, without asking prior permission from the publisher or the author. This Article is brought to you for free and open access by ScholarWorks@UARK. It has been accepted for inclusion in Journal of the Arkansas Academy of Science by an authorized editor of ScholarWorks@UARK. For more information, please contact [email protected], [email protected]. Journal of the Arkansas Academy of Science, Vol. 61 [2007], Art. 17 -I Distribution of the Queen Snake (Regina septemvittata) in Arkansas llinOiS./ JONATHAN W. STANLEyl,2 AND STANLEY E. TRAUTH1 ~orgia. lDepartment ofBiological Sciences, Arkansas State University, PO Box 599, State University, AR 72467-0599 rabbi! NOods /. torrespondence: [email protected] I [MS , i ~rslty. I Abstract.-We documented the distribution ofthe queen snake, Regina septemvittata, in northern Arkansas during the 2005 and 2006 activity seasons.
    [Show full text]
  • 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.
    [Show full text]
  • American Toad (Anaxyrus Americanus) Fowler's Toad (Anaxyrus Fowleri
    Vermont has eleven known breeding species of frogs. Their exact distributions are still being determined. In order for these species to survive and flourish, they need our help. One way you can help is to report the frogs that you come across in the state. Include in your report as much detail as you can on the appearance and location of the animal; also include the date of the sighting, your name, and how to contact you. Photographs are ideal, but not necessary. When attempting to identify a particular species, check at least three different field markings so that you can be sure of what it is. To contribute a report, you may use our website (www.vtherpatlas.org) or contact Jim Andrews directly at [email protected]. American Bullfrog (Lithobates catesbeianus) American Toad (Anaxyrus americanus) The American Bullfrog is our largest frog and can reach 7 inches long. The Bullfrog is one of the three The American Toad is one of Vermont’s two toad species. Toads can be distinguished from other green-faced frogs in Vermont. It has a green and brown mottled body with dark stripes across its legs. frogs in Vermont by their dry and bumpy skin, and the long oval parotoid glands on each side of their The Bullfrog does not have dorsolateral ridges, but it does have a ridge that starts at the eye and goes necks. The American Toad has at least one large wart in each of the large black spots found along its around the eardrum (tympana) and down. The Bullfrog’s call is a deep low jum-a-rum.
    [Show full text]
  • Tail Bifurcation in Plestiodon Skiltonianus
    Herpetology Notes, volume 13: 343-345 (2020) (published online on 23 April 2020) Tail bifurcation in Plestiodon skiltonianus Danielle C. Miles1,*, Chasey L. Danser1, and Kevin T. Shoemaker1 Plestiodon skiltonianus (Smith, 2005), commonly The majority of tail bifurcations in other lizard species known as the Western Skink, is a smooth-scaled species are likely the result of abnormal tail regeneration after with a range from southern Idaho to northern Arizona in a lizard sheds its tail in response to a threat and are the Western United States (Tanner, 1957). The Western common across several lizard families (Clause et al. Skink is a part of the evolutionarily related skiltonianus 2006; Conzendey et al. 2013; Dudek & Ekner-Grzyb, group of lizards, of which none have previous records of 2014; Pelegrin & Leão, 2016; Tamar et al. 2013). Caudal tail bifurcation that we could find (Richmond & Reeder, 2002). Tail bifurcation is found in all of the major lizard groups and the most closely related species with this recorded observation is Plestiodon inexpectatus (Brandley et al, 2012; Koleska et al, 2017; Mitchell et al, 2012). On July 13 2019, one P. skiltonianus with a bifurcated tail was captured in a medium Sherman aluminium box trap designed for the live capture of small mammals that had been baited with bird seed and filled with biodegradable batting. As the traps were being collected at 17:00 PST, the malformed individual was found in the back of a trap, though the trap had not been triggered by its weight. The field site is at 39.4993°N, -117.0053°E on United States Forest Service land in Lander County northeast of Austin, Nevada, USA at an elevation of 1920 meters.
    [Show full text]
  • 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.
    [Show full text]
  • Snakes of the Everglades Agricultural Area1 Michelle L
    CIR1462 Snakes of the Everglades Agricultural Area1 Michelle L. Casler, Elise V. Pearlstine, Frank J. Mazzotti, and Kenneth L. Krysko2 Background snakes are often escapees or are released deliberately and illegally by owners who can no longer care for them. Snakes are members of the vertebrate order Squamata However, there has been no documentation of these snakes (suborder Serpentes) and are most closely related to lizards breeding in the EAA (Tennant 1997). (suborder Sauria). All snakes are legless and have elongated trunks. They can be found in a variety of habitats and are able to climb trees; swim through streams, lakes, or oceans; Benefits of Snakes and move across sand or through leaf litter in a forest. Snakes are an important part of the environment and play Often secretive, they rely on scent rather than vision for a role in keeping the balance of nature. They aid in the social and predatory behaviors. A snake’s skull is highly control of rodents and invertebrates. Also, some snakes modified and has a great degree of flexibility, called cranial prey on other snakes. The Florida kingsnake (Lampropeltis kinesis, that allows it to swallow prey much larger than its getula floridana), for example, prefers snakes as prey and head. will even eat venomous species. Snakes also provide a food source for other animals such as birds and alligators. Of the 45 snake species (70 subspecies) that occur through- out Florida, 23 may be found in the Everglades Agricultural Snake Conservation Area (EAA). Of the 23, only four are venomous. The venomous species that may occur in the EAA are the coral Loss of habitat is the most significant problem facing many snake (Micrurus fulvius fulvius), Florida cottonmouth wildlife species in Florida, snakes included.
    [Show full text]
  • Common Species
    Common Species on District Lands The Southwest Florida Water Management District (District) manages water resources in the west- central portion of Florida according to legislative mandates. The District uses public land acquisition funds to protect key lands for water resources. The natural communities, plants and animals on these lands also benefi t from a level of protection that can be experienced and enjoyed through recreational opportunities made available on District lands. Every year, approximately 2.5 million people visit the more than 436,000 acres of public conservation lands acquired by the District and its partners. The lands are open to the public for activities such as hiking, bicycling, hunting, horseback riding, fi shing, camping, picnicking and studying nature. The District provides these recreational opportunities so that residents may experience healthy natural communities. An array of natural landscapes is available from the meandering Outstanding Florida Southwest Florida Water Management District Waters riverine systems, the cypress domes and strands, swamps and hammocks, to the scrub, sandhill, and pine fl atwoods. The Common Species on District Lands brochure provides insight to what you may experience while recreating on public lands managed by the District. CONSERVATION LANDS Southwest Florida Water Management District Mammals Southwest Florida Water Management District iStock W Barbour - Smithsonian Institute Roger Virginia Brazilian Opossum Free-Tailed Bat Didelphis virginiana Tadarida brasiliensis iStock Ivy
    [Show full text]