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Eastern Cottontail Rabbits (Sylvilagus Floridanus)
Publication WSFNR-20-58A July 2020 Managing Wildlife Damage: Eastern Cottontail Rabbits (Sylvilagus floridanus) Joseph Brown, UGA Warnell School of Forestry & Natural Resources Michael T. Mengak, UGA Warnell School of Forestry & Natural Resources INTRODUCTION Eastern cottontail rabbits (Sylvilagus floridanus) are found across the eastern United States, southern Canada, eastern Mexico, Central America and portions of South America (Figure 1). Cottontail rabbits are a sought-after game species by small game hunters. Many people enjoy seeing them around their yards and neighborhoods. Rabbits are well accepted by humans when their numbers are managed correctly. However, they can inflict damage across a range of habitats from rural farms to suburban lawns. They often damage flowers, vegetable gardens, and landscape trees and shrubs. TAXONOMY Class Mammalia Order Lagomorpha Family Leporidae Genus - Sylvilagus Species – floridanus Common Name - Eastern cottontail rabbit There are 11 genera and 54 species in Leporidae which includes hares and rabbits. Six species of cottontail rabbits are found in the genus Sylvilagus. The scientific name, Sylvilagus floridanus, means forest hare of Florida. Figure 1: Current eastern cottontail STATUS distribution across North and Central America. In Georgia, we have 4 native species of rabbits. The swamp rabbit (Sylvilagus aquaticus), Appalachian cottontail (S. obscurus), marsh rabbit (S. palustris), and eastern cottontail (S. floridanus). The eastern cottontail (Figure 2) is the most abundant and ranges across the entire state. The Appalachian cottontail is the rarest rabbit and inhabits the start of the Appalachian mountain chain in North Georgia. It is on the Georgia Protected Wildlife list. The swamp rabbit is the largest of the four and inhabits swamps in the Piedmont region of Georgia. -
Population Structure of the Lower Keys Marsh Rabbit As Determined by Mitochondrial DNA Analysis
Management and Conservation Note Population Structure of the Lower Keys Marsh Rabbit as Determined by Mitochondrial DNA Analysis AMANDA L. CROUSE, College of Veterinary Medicine, Texas A&M University, College Station, TX 77843-4461, USA RODNEY L. HONEYCUTT, Natural Science Division, Pepperdine University, Malibu, CA 90263-4321, USA ROBERT A. MCCLEERY,1 Department of Wildlife and Fisheries Sciences, Texas A&M University, College Station, TX 77843-2258, USA CRAIG A. FAULHABER, Department of Wildland Resources, Utah State University, Logan, UT 84322-5230, USA NEIL D. PERRY, Utah Division of Wildlife Resources, Cedar City, UT 84270-0606, USA ROEL R. LOPEZ, Department of Wildlife and Fisheries Sciences, Texas A&M University, College Station, TX 77843-2258, USA ABSTRACT We used nucleotide sequence data from a mitochondrial DNA fragment to characterize variation within the endangered Lower Keys marsh rabbit (Sylvilagus palustris hefneri). We observed 5 unique mitochondrial haplotypes across different sampling sites in the Lower Florida Keys, USA. Based on the frequency of these haplotypes at different geographic locations and relationships among haplotypes, we observed 2 distinct clades or groups of sampling sites (western and eastern clades). These 2 groups showed low levels of gene flow. Regardless of their origin, marsh rabbits from the Lower Florida Keys can be separated into 2 genetically distinct management units, which should be considered prior to implementation of translocations as a means of offsetting recent population declines. (JOURNAL OF WILDLIFE MANAGEMENT 73(3):362–367; 2009) DOI: 10.2193/2007-207 KEY WORDS Florida Keys, genetic, marsh rabbit, mitochondrial DNA, population structure, Sylvilagus palustris hefneri. The Lower Keys marsh rabbit (Sylvilagus palustris hefneri)is (Forys and Humphrey 1999b). -
Informes Individuales IUCN 2018.Indd
IUCN SSC Lagomorph Specialist Group 2018 Report Andrew Smith Hayley Lanier Co-Chairs Mission statement Targets for the 2017-2020 quadrennium Andrew Smith (1) To promote the conservation and effective Assess (2) Hayley Lanier sustainable management of all species of Red List: (1) improve knowledge and assess- lagomorph through science, education and ment of lagomorph systematics, (2) complete Red List Authority Coordinator advocacy. all Red List reassessments of all lagomorph Charlotte Johnston (1) species. Projected impact for the 2017-2020 Research activities: (1) improve knowledge of Location/Affiliation quadrennium Brachylagus idahoensis; (2) examine popula- (1) School of Life Sciences, Arizona State The Lagomorph Specialist Group (LSG) is tion trends of all lagomorphs in the western University, Tempe, Arizona, US “middle-sized” – not a single species, nor United States; (3) improve knowledge of Lepus (2) Sam Noble Museum, University of Oklahoma, composed of hundreds of species. We have callotis; (4) improve knowledge of Lepus fagani, Norman, Oklahoma, US slightly less than 100 species in our brief. L. habessinicus, and L. starcki in Ethiopia; However, these are distributed around the (5) improve knowledge of Lepus flavigularis; Number of members globe, and there are few similarities among (6) improve knowledge of all Chinese Lepus; 73 any of our many forms that are Red List clas- (7) improve knowledge of Nesolagus netscheri; sified as Threatened. Thus, we do not have a (8) improve knowledge of Nesolagus timminsi; Social networks single programme or a single thrust; there is no (9) improve knowledge of Ochotona iliensis; Website: one-size-fits-all to our approach. LSG members (10) improve surveys of poorly-studied www.lagomorphspecialistgroup.org largely work independently in their region, and Ochotona in China; (11) understand the role the Co-Chairs serve more as a nerve centre. -
Appendix Lagomorph Species: Geographical Distribution and Conservation Status
Appendix Lagomorph Species: Geographical Distribution and Conservation Status PAULO C. ALVES1* AND KLAUS HACKLÄNDER2 Lagomorph taxonomy is traditionally controversy, and as a consequence the number of species varies according to different publications. Although this can be due to the conservative characteristic of some morphological and genetic traits, like general shape and number of chromosomes, the scarce knowledge on several species is probably the main reason for this controversy. Also, some species have been discovered only recently, and from others we miss any information since they have been first described (mainly in pikas). We struggled with this difficulty during the work on this book, and decide to include a list of lagomorph species (Table 1). As a reference, we used the recent list published by Hoffmann and Smith (2005) in the “Mammals of the world” (Wilson and Reeder, 2005). However, to make an updated list, we include some significant published data (Friedmann and Daly 2004) and the contribu- tions and comments of some lagomorph specialist, namely Andrew Smith, John Litvaitis, Terrence Robinson, Andrew Smith, Franz Suchentrunk, and from the Mexican lagomorph association, AMCELA. We also include sum- mary information about the geographical range of all species and the current IUCN conservation status. Inevitably, this list still contains some incorrect information. However, a permanently updated lagomorph list will be pro- vided via the World Lagomorph Society (www.worldlagomorphsociety.org). 1 CIBIO, Centro de Investigaça˜o em Biodiversidade e Recursos Genéticos and Faculdade de Ciˆencias, Universidade do Porto, Campus Agrário de Vaira˜o 4485-661 – Vaira˜o, Portugal 2 Institute of Wildlife Biology and Game Management, University of Natural Resources and Applied Life Sciences, Gregor-Mendel-Str. -
Estimating Diet and Food Selectivity of the Lower Keys Marsh Rabbit Using Stable Isotope Analysis
ESTIMATING DIET AND FOOD SELECTIVITY OF THE LOWER KEYS MARSH RABBIT USING STABLE ISOTOPE ANALYSIS by MATTHEW JAMES GORDON B.S. Florida State University, 2008 A thesis submitted in partial fulfillment of the requirements for the degree of Master of Science in the Department of Biology in the College of Sciences at the University of Central Florida Orlando, Florida Fall Term 2010 Major Professor: Eric A. Hoffman © 2010 Matthew Gordon ii ABSTRACT Understanding the effect of food abundance on feeding behavior can benefit conservation efforts in many ways, such as to determine whether impacted environments need food supplementation, whether different locations of threatened species contain different food abundances, or whether reintroduction sites are missing key components of a species’ diet. I studied the relationship between feeding behavior and food abundance in the Lower Keys marsh rabbit (Sylvilagus palustris hefneri), an endangered subspecies endemic to the lower Florida Keys. Specifically, my study set out to measure the relative abundance of the primary plants within the natural habitat of the Lower Keys marsh rabbit and estimate the proportion of each of these plants within the rabbit’s diet. With this information, I tested the following hypotheses: first, the Lower Keys marsh rabbit selectively feeds on specific plants; second, that diet does not differ among sites; and third, that diet is not affected by food abundance. Using stable isotope analysis, I determined that two plants were prominent in the rabbit’s diet: a shrub, Borrichia frutescens, and a grass, Spartina spartinae. These two species were prominent in the rabbit’s diet in most patches, even where they were relatively rare, suggesting the rabbits are indeed selectively feeding on these species. -
A Brief Overview of Rabbit Survey Methodology
A Brief Overview of Rabbit Survey Methodology Prepared by: Robin Russell U.S. Geological Survey, National Wildlife Health Center, Madison, WI, ([email protected]);Todd Esque U.S. Geological Survey, Western Ecological Research Center, Henderson, NV, ([email protected]); Matthew Gompper Department of Fish, Wildlife and Conservation Ecology, New Mexico State University, Las Cruces, NM ([email protected]); Gary Roemer Department of Fish, Wildlife and Conservation Ecology, New Mexico State University, Las Cruces, NM, ([email protected]) Rabbit populations (including North American native or feral domestic species of the genera Brachylagus, Lepus, Oryctolagus and Sylvilagus) can be estimated from surveys using a variety of approaches. Below we provide a brief description of survey methods for rabbits, with additional details in the referenced literature. We cover survey methods that estimate presence/absence, relative abundance, abundance estimates from mark-recapture, and distance sampling. Choice of study design should depend on objectives and available resources. Please contact the authors for assistance with study designs that meet objectives within resource constraints. Consulting a statistician prior to beginning any surveillance program is recommended. Presence/Absence In general presence/absence estimates are used to elucidate patterns in how a species uses available habitat. Although not as sensitive to changes in abundance as other population-level metrics (see below), presence/absence can nonetheless be a useful tool for evaluating landscape-level changes in species distributions and resource use. Presence/absence data can be summarized within the framework of occupancy modeling (MacKenzie et al. 2006). Occupancy estimates are generated from repeat visits to the same location over a short period of time within which the population can assume to be demographically and geographically closed (i.e. -
Marsh Rabbit, Sylvilagus Palustris (Lagomorpha: Florida, USA
Sylvilagus palustris (Bachman, 1837) MARB Brian R. Chapman and Margaret K. Trani CONTENT AND TAXONOMIC COMMENTS Three subspecies of marsh rabbit (Sylvilagus palustris) are recognized: S. p. palustris, S. p. paludicola,andS. p. hefneri (Lazell 1984). Literature on the marsh rabbit is reviewed by Chapman and Willner (1981) and Chap- man et al. (1982). DISTINGUISHING CHARACTERISTICS The marsh rabbit is a moderate-sized cottontail. Mea- surements are: total length, 400–450 mm; tail, 30–40 mm; hind foot, 85–100 mm; ear, 45–55 mm; weight, 1.0–2.2 kg. The dorsal parts of head and body may vary from chestnut brown to rusty red, but all speci- mens have a dark cinnamon nape. The middle of abdomen is white and the remainder of belly is pale brown to buff. The feet are slender and reddish to buffy. The ventral surface of the tail, unlike other Sylvilagus, is dingy gray. The basilar length of the skull of S. palustris is usually less than 63 mm. The anterior portion of the supraorbital process is typically absent and the posterior portion of the supraorbital process is fused to the skull. The dental formula is: I 2/1, C 0/0, P 3/2, M 3/3 = 28 (Figure 1). Marsh rab- bits may be confused with swamp rabbits (S. aquaticus) and eastern cottontails (S. floridanus). Marsh rabbits usually are distinguishable from both species due to a larger body size and a gray tail. Marsh rabbits also possess a black spot between the ears, which is absent in the eastern cottontail. CONSERVATION STATUS The marsh rabbit has a global rank of Secure (NatureServe 2007). -
Lagomorphs: Pikas, Rabbits, and Hares of the World
LAGOMORPHS 1709048_int_cc2015.indd 1 15/9/2017 15:59 1709048_int_cc2015.indd 2 15/9/2017 15:59 Lagomorphs Pikas, Rabbits, and Hares of the World edited by Andrew T. Smith Charlotte H. Johnston Paulo C. Alves Klaus Hackländer JOHNS HOPKINS UNIVERSITY PRESS | baltimore 1709048_int_cc2015.indd 3 15/9/2017 15:59 © 2018 Johns Hopkins University Press All rights reserved. Published 2018 Printed in China on acid- free paper 9 8 7 6 5 4 3 2 1 Johns Hopkins University Press 2715 North Charles Street Baltimore, Maryland 21218-4363 www .press .jhu .edu Library of Congress Cataloging-in-Publication Data Names: Smith, Andrew T., 1946–, editor. Title: Lagomorphs : pikas, rabbits, and hares of the world / edited by Andrew T. Smith, Charlotte H. Johnston, Paulo C. Alves, Klaus Hackländer. Description: Baltimore : Johns Hopkins University Press, 2018. | Includes bibliographical references and index. Identifiers: LCCN 2017004268| ISBN 9781421423401 (hardcover) | ISBN 1421423405 (hardcover) | ISBN 9781421423418 (electronic) | ISBN 1421423413 (electronic) Subjects: LCSH: Lagomorpha. | BISAC: SCIENCE / Life Sciences / Biology / General. | SCIENCE / Life Sciences / Zoology / Mammals. | SCIENCE / Reference. Classification: LCC QL737.L3 L35 2018 | DDC 599.32—dc23 LC record available at https://lccn.loc.gov/2017004268 A catalog record for this book is available from the British Library. Frontispiece, top to bottom: courtesy Behzad Farahanchi, courtesy David E. Brown, and © Alessandro Calabrese. Special discounts are available for bulk purchases of this book. For more information, please contact Special Sales at 410-516-6936 or specialsales @press .jhu .edu. Johns Hopkins University Press uses environmentally friendly book materials, including recycled text paper that is composed of at least 30 percent post- consumer waste, whenever possible. -
Springer International Publishing AG, Part of Springer Nature 2018 J
L Lagomorpha Navigation to guide their movements in the landscape and the timing thereof. Anthony Caravaggi The order Lagomorpha is comprised of two School of Biological Earth and Environmental families, the hares and rabbits (Leporidae or Sciences, University College Cork, Cork, Ireland leporids) and the pikas (Ochotonidae). The navi- School of Biological Sciences, Medical Biology gational capabilities of lagomorphs are poorly Centre, Queen’s University Belfast, Belfast, UK understood, with the few movement studies to have been conducted focusing on dispersal, home range behavior, foraging, and habitat use. Synonyms Indeed, movement behavior has been entirely unstudied in most lagomorph species. Studying Behavior; Hare; Movement; Pika; Rabbit the navigational capabilities of small-to-medium- sized mammals can be challenging as the equip- ment required for fine-scale data collection (e.g., GPS collars) are often too heavy and/or have Definition limited battery life. For example, the maximum weight for GPS collars is defined by the size of the – Navigation the theory and practice of charting a subject. This is known as the “5% rule” (Cochran course to a remote goal (Schöne 1984). 1980); the weight of the collar should not exceed 5% of the focal animal’s mass. For a very large hare weighing 5 kg, that would equate to a GPS Introduction collar weighing 250 g. The typical battery life for such a collar is around 500 days, though that is The daily movements of animals are governed by based on the recording of only a handful of “fixes” many factors including the need to find food, (i.e., records of the individual’s location) per day – water, conspecifics, and favorable environmental not enough for nuanced analysis of movement conditions while trying to avoid predators, domi- behavior such as navigational strategies nant ecological competitors, and unfavorable hab- (Handcock et al. -
TCP Wildlife List
Wildlife Species List for Telegraph Creek Preserve Designated Status Scientific Name Common Name FWC FWS FNAI MAMMALS Family: Didelphidae (opossums) Didelphis virginiana Virginia opossum Family: Dasypodidae (armadillos) Dasypus novemcinctus nine-banded armadillo * Family: Sciuridae (squirrels and their allies) Sciurus carolinensis eastern gray squirrel Family: Muridae (mice and rats) Peromyscus gossypinus cotton mouse Sigmodon hispidus hispid cotton rat Family: Leporidae (rabbits and hares) Sylvilagus palustris marsh rabbit Sylvilagus floridanus eastern cottontail Family: Felidae (cats) Puma concolor coryi Florida panther E E G5T1/S1 Lynx rufus bobcat Family: Canidae (wolves and foxes) Canis latrans coyote Urocyon cinereoargenteus common gray fox Family: Procyonidae (raccoons) Procyon lotor raccoon Family: Mustelidae (weasels, otters and relatives) Lutra canadensis northern river otter Family: Suidae (old world swine) Sus scrofa feral hog * Family: Cervidae (deer) Odocoileus virginianus white-tailed deer BIRDS Family: Anatidae (swans, geese and ducks) Subfamily: Dendrocygninae Dendrocygna autumnalis black-bellied whistling duck Subfamily: Anatinae Cairina moschata muscovy duck * Anas fulvigula mottled duck Family: Odontophoridae (new world quails) Colinus virginianus northern bobwhite Family: Phasianidae (pheasant, grouse, turkeys and their allies) Subfamily: Meleagridinae (turkeys) Meleagris gallopavo wild turkey Family: Ciconiidae (storks) Mycteria americana wood stork E E G4/S2 Family: Phalacrocoracidae (cormorants) Phalacrocorax auritus -
Swamp Rabbit Sylvilagus Aquaticus Contributors: Mary Bunch, Steven G
Swamp Rabbit Sylvilagus aquaticus Contributors: Mary Bunch, Steven G. Platt and Stanlee Miller DESCRIPTION Taxonomy and Basic Description The swamp rabbit, Sylvilagus aquaticus, was first described by Bachman in 1837. Swamp rabbits, or cane-cutters, are the largest species of rabbit in the southeastern United States. These rabbits range in total length from 452 to 552 mm (17.8 to 21.7 inches) and range from 1900 to 2700 g (4.5 to 6 pounds) in weight (Chapman and Feldhamer 1981; Webster et al. 1985). Weights of South Carolina specimens in the Campbell Photo by Ted Borg Museum of Natural History at Clemson University range from 1700 to 2300 g (3.74 to 5.07 pounds). The fur of swamp rabbits is rusty-brown with black hairs, giving the animals a grizzled appearance. Similar to the eastern cottontail (Sylvilagus floridanus) and the Appalachian cottontail (Sylvilagus obscurus), the underside of the tail is white. This differs from the bluish gray tail of the marsh rabbit (Sylvilagus palustris). There are two recognized subspecies of swamp rabbit: Sylvilagus aquaticus aquaticus and Sylvilagus aquaticus littoralis. The former is the only subspecies found in South Carolina and the latter is restricted to the Gulf Coast (Hall and Kelson 1959; Chapman and Feldhamer 1981). Status In South Carolina, these rabbits are considered rare or imperiled (S2/S3) due to habitat loss and limited habitat availability. In Alabama and neighboring Georgia, the swamp rabbit is ranked as secure, while in Tennessee the species is apparently secure. The Global Heritage Rank is secure or G5 (NatureServe 2004), yet data from several states, including Arkansas, Missouri and Kentucky, indicate populations are imperiled due to loss of habitat (Platt and Bunch 2000) and range shrinkage (Sealander and Heidt 1990; Schwartz and Schwartz 1981; Sole 1994). -
Rabbits, Hares and Pikas Status Survey and Conservation Action Plan
-Rabbits, Hares and Pikas Status Survey and Conservation Action Plan Compiled and edited by Joseph A. Chapman and John E.C. Flux IUCN/SSC Lagomorph Specialist Group Rabbits, Hares and Pikas Status Survey and Action Plan Compiled and edited by Joseph A. Chapman and John E.C. Flux IUCN/SSC Lagomorph Specialist Group of Oman Foreword The IUCN/SSC Lagomorph Specialist Group was constituted The Lagomorph Group, building on its good start, soon as- in as part of a determined effort by the Species Survival sumed responsibility for providing the information necessary Commission to broaden the base of its activities by incorporat- for preparing and updating lagomorph entries in the Red Data ing a large number of new Groups into its membership. By the Book and for submissions to the Convention on International end of 1979, the Lagomorph Group had attracted from Europe, Trade in Endangered Species of Wild Fauna and Flora Asia, Africa, the Americas and the Pacific 19 highly motivated (CITES). It holds a strong position against the introduction of biologists with a concern for problems of conservation of the eastern cottontail to Europe, and has gomorphs in their respective lands, and a willingness to do willingly participated in discussions on the subject when re- something about them. quested. The Group also continues to take the lead in keeping In August 1979, the young Group held its inaugural meeting lagomorphs on conference agenda at international meetings, at the University of Guelph, Ontario, in conjunction with the and has widened its in recent years to look at the status first World Lagomorph Conference.