Comparative Phylogeography and a Mitochondrial DNA Barcode for Identifying Three Sympatric Lagomorphs in the Northeastern United States
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Learning About Mammals
Learning About Mammals The mammals (Class Mammalia) includes everything from mice to elephants, bats to whales and, of course, man. The amazing diversity of mammals is what has allowed them to live in any habitat from desert to arctic to the deep ocean. They live in trees, they live on the ground, they live underground, and in caves. Some are active during the day (diurnal), while some are active at night (nocturnal) and some are just active at dawn and dusk (crepuscular). They live alone (solitary) or in great herds (gregarious). They mate for life (monogamous) or form harems (polygamous). They eat meat (carnivores), they eat plants (herbivores) and they eat both (omnivores). They fill every niche imaginable. Mammals come in all shapes and sizes from the tiny pygmy shrew, weighing 1/10 of an ounce (2.8 grams), to the blue whale, weighing more than 300,000 pounds! They have a huge variation in life span from a small rodent living one year to an elephant living 70 years. Generally, the bigger the mammal, the longer the life span, except for bats, which are as small as rodents, but can live for up to 20 years. Though huge variation exists in mammals, there are a few physical traits that unite them. 1) Mammals are covered with body hair (fur). Though marine mammals, like dolphins and whales, have traded the benefits of body hair for better aerodynamics for traveling in water, they do still have some bristly hair on their faces (and embryonically - before birth). Hair is important for keeping mammals warm in cold climates, protecting them from sunburn and scratches, and used to warn off others, like when a dog raises the hair on its neck. -
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. -
Mammal Species Native to the USA and Canada for Which the MIL Has an Image (296) 31 July 2021
Mammal species native to the USA and Canada for which the MIL has an image (296) 31 July 2021 ARTIODACTYLA (includes CETACEA) (38) ANTILOCAPRIDAE - pronghorns Antilocapra americana - Pronghorn BALAENIDAE - bowheads and right whales 1. Balaena mysticetus – Bowhead Whale BALAENOPTERIDAE -rorqual whales 1. Balaenoptera acutorostrata – Common Minke Whale 2. Balaenoptera borealis - Sei Whale 3. Balaenoptera brydei - Bryde’s Whale 4. Balaenoptera musculus - Blue Whale 5. Balaenoptera physalus - Fin Whale 6. Eschrichtius robustus - Gray Whale 7. Megaptera novaeangliae - Humpback Whale BOVIDAE - cattle, sheep, goats, and antelopes 1. Bos bison - American Bison 2. Oreamnos americanus - Mountain Goat 3. Ovibos moschatus - Muskox 4. Ovis canadensis - Bighorn Sheep 5. Ovis dalli - Thinhorn Sheep CERVIDAE - deer 1. Alces alces - Moose 2. Cervus canadensis - Wapiti (Elk) 3. Odocoileus hemionus - Mule Deer 4. Odocoileus virginianus - White-tailed Deer 5. Rangifer tarandus -Caribou DELPHINIDAE - ocean dolphins 1. Delphinus delphis - Common Dolphin 2. Globicephala macrorhynchus - Short-finned Pilot Whale 3. Grampus griseus - Risso's Dolphin 4. Lagenorhynchus albirostris - White-beaked Dolphin 5. Lissodelphis borealis - Northern Right-whale Dolphin 6. Orcinus orca - Killer Whale 7. Peponocephala electra - Melon-headed Whale 8. Pseudorca crassidens - False Killer Whale 9. Sagmatias obliquidens - Pacific White-sided Dolphin 10. Stenella coeruleoalba - Striped Dolphin 11. Stenella frontalis – Atlantic Spotted Dolphin 12. Steno bredanensis - Rough-toothed Dolphin 13. Tursiops truncatus - Common Bottlenose Dolphin MONODONTIDAE - narwhals, belugas 1. Delphinapterus leucas - Beluga 2. Monodon monoceros - Narwhal PHOCOENIDAE - porpoises 1. Phocoena phocoena - Harbor Porpoise 2. Phocoenoides dalli - Dall’s Porpoise PHYSETERIDAE - sperm whales Physeter macrocephalus – Sperm Whale TAYASSUIDAE - peccaries Dicotyles tajacu - Collared Peccary CARNIVORA (48) CANIDAE - dogs 1. Canis latrans - Coyote 2. -
Colorado Field Ornithologists the Colorado Field Ornithologists' Quarterly
Journal of the Colorado Field Ornithologists The Colorado Field Ornithologists' Quarterly VOL. 36, NO. 1 Journal of the Colorado Field Ornithologists January 2002 Vol. 36, No. 1 Journal of the Colorado Field Ornithologists January 2002 TABLE OF C ONTENTS A LETTER FROM THE E DITOR..............................................................................................2 2002 CONVENTION IN DURANGO WITH KENN KAUFMANN...................................................3 CFO BOARD MEETING MINUTES: 1 DECEMBER 2001........................................................4 TREE-NESTING HABITAT OF PURPLE MARTINS IN COLORADO.................................................6 Richard T. Reynolds, David P. Kane, and Deborah M. Finch OLIN SEWALL PETTINGILL, JR.: AN APPRECIATION...........................................................14 Paul Baicich MAMMALS IN GREAT HORNED OWL PELLETS FROM BOULDER COUNTY, COLORADO............16 Rebecca E. Marvil and Alexander Cruz UPCOMING CFO FIELD TRIPS.........................................................................................23 THE SHRIKES OF DEARING ROAD, EL PASO COUNTY, COLORADO 1993-2001....................24 Susan H. Craig RING-BILLED GULLS FEEDING ON RUSSIAN-OLIVE FRUIT...................................................32 Nicholas Komar NEWS FROM THE C OLORADO BIRD R ECORDS COMMITTEE (JANUARY 2002).........................35 Tony Leukering NEWS FROM THE FIELD: THE SUMMER 2001 REPORT (JUNE - JULY)...................................36 Christopher L. Wood and Lawrence S. Semo COLORADO F IELD O -
World Distribution of the European Rabbit (Oryctolagus Cuniculus)
1 The Evolution, Domestication and World Distribution of the European Rabbit (Oryctolagus cuniculus) Luca Fontanesi1*, Valerio Joe Utzeri1 and Anisa Ribani1 1Department of Agricultural and Food Sciences, Division of Animal Sciences, University of Bologna, Italy 1.1 The Order Lagomorpha to assure essential vitamin uptake, the digestion of the vegetarian diet and water reintroduction The European rabbit (Oryctolagus cuniculus, (Hörnicke, 1981). Linnaeus 1758) is a mammal belonging to the The order Lagomorpha was recognized as a order Lagomorpha. distinct order within the class Mammalia in Lagomorphs are such a distinct group of 1912, separated from the order Rodentia within mammalian herbivores that the very word ‘lago- which lagomorphs were originally placed (Gidely, morph’ is a circular reference meaning ‘hare- 1912; Landry, 1999). Lagomorphs are, however, shaped’ (Chapman and Flux, 1990; Fontanesi considered to be closely related to the rodents et al., 2016). A unique anatomical feature that from which they diverged about 62–100 million characterizes lagomorphs is the presence of years ago (Mya), and together they constitute small peg-like teeth immediately behind the up- the clade Glires (Chuan-Kuei et al., 1987; Benton per-front incisors. For this feature, lagomorphs and Donoghue, 2007). Lagomorphs, rodents and are also known as Duplicidentata. Therefore, primates are placed in the major mammalian instead of four incisor teeth characteristic of clade of the Euarchontoglires (O’Leary et al., 2013). rodents (also known as Simplicidentata), lago- Modern lagomorphs might be evolved from morphs have six. The additional pair is reduced the ancestral lineage from which derived the in size. Another anatomical characteristic of the †Mimotonidae and †Eurymilydae sister taxa, animals of this order is the presence of an elong- following the Cretaceous-Paleogene (K-Pg) bound- ated rostrum of the skull, reinforced by a lattice- ary around 65 Mya (Averianov, 1994; Meng et al., work of bone, which is a fenestration to reduce 2003; Asher et al., 2005; López-Martínez, 2008). -
(Sylvilagus Transitionalis) and Cross‑Amplifcation in the Eastern Cottontail (S
King et al. BMC Res Notes (2017) 10:741 https://doi.org/10.1186/s13104-017-3062-2 BMC Research Notes RESEARCH NOTE Open Access Microsatellite marker development from next‑generation sequencing in the New England cottontail (Sylvilagus transitionalis) and cross‑amplifcation in the eastern cottontail (S. foridanus) Timothy L. King1, Michael Eackles1, Aaron Aunins2*, Thomas J. McGreevy Jr.3, Thomas P. Husband3, Anthony Tur4 and Adrienne I. Kovach5 Abstract Objective: The New England cottontail (Sylvilagus transitionalis) is a species of high conservation priority in the Northeastern United States, and was a candidate for federal listing under the Endangered Species Act until a recent decision determined that conservation actions were sufcient to preclude listing. The aim of this study was to develop a suite of microsatellite loci to guide future research eforts such as the analysis of population genetic struc- ture, genetic variation, dispersal, and genetic mark-recapture population estimation. Results: Thirty-fve microsatellite markers containing tri- and tetranucleotide sequences were developed from shotgun genomic sequencing of tissue from S. transitionalis, S. obscurus, and S. foridanus. These loci were screened in n 33 wild S. transitionalis sampled from a population in eastern Massachusetts, USA. Thirty-two of the 35 loci were polymorphic= with 2–6 alleles, and observed heterozygosities of 0.06–0.82. All loci conformed to Hardy–Weinberg Equilibrium proportions and there was no evidence of linkage disequilibrium or null alleles. Primers for 33 of the 35 loci amplifed DNA extracted from n 6 eastern cottontail (S. foridanus) samples, of which nine revealed putative species-diagnostic alleles. These loci =will provide a useful tool for conservation genetics investigations of S. -
Genomic Analysis Reveals Hidden Biodiversity Within Colugos, the Sister Group to Primates Victor C
Washington University School of Medicine Digital Commons@Becker Open Access Publications 2016 Genomic analysis reveals hidden biodiversity within colugos, the sister group to primates Victor C. Mason Texas A & M University - College Station Gang Li Texas A & M University - College Station Patrick Minx Washington University School of Medicine in St. Louis Jürgen Schmitz University of Münster Gennady Churakov University of Münster See next page for additional authors Follow this and additional works at: https://digitalcommons.wustl.edu/open_access_pubs Recommended Citation Mason, Victor C.; Li, Gang; Minx, Patrick; Schmitz, Jürgen; Churakov, Gennady; Doronina, Liliya; Melin, Amanda D.; Dominy, Nathaniel J.; Lim, Norman T-L; Springer, Mark S.; Wilson, Richard K.; Warren, Wesley C.; Helgen, Kristofer M.; and Murphy, William J., ,"Genomic analysis reveals hidden biodiversity within colugos, the sister group to primates." Science Advances.2,8. e1600633. (2016). https://digitalcommons.wustl.edu/open_access_pubs/5209 This Open Access Publication is brought to you for free and open access by Digital Commons@Becker. It has been accepted for inclusion in Open Access Publications by an authorized administrator of Digital Commons@Becker. For more information, please contact [email protected]. Authors Victor C. Mason, Gang Li, Patrick Minx, Jürgen Schmitz, Gennady Churakov, Liliya Doronina, Amanda D. Melin, Nathaniel J. Dominy, Norman T-L Lim, Mark S. Springer, Richard K. Wilson, Wesley C. Warren, Kristofer M. Helgen, and William J. Murphy This open access publication is available at Digital Commons@Becker: https://digitalcommons.wustl.edu/open_access_pubs/5209 RESEARCH ARTICLE ZOOLOGICAL POPULATION GENETICS 2016 © The Authors, some rights reserved; exclusive licensee American Association for the Advancement of Science. -
Best Management Practices for the New England Cottontail - New York
Best Management Practices For the New England Cottontail New York Specific challenges Invasive shrubs Heathlands Canopy Retention Eastern cottontails Statement of Purpose Populations of species residing at the edge of their range are exposed to novel environments and stressors that may affect their response to management. The impacts of eastern cottontails and the prevalence of invasive shrubs have been recognized as factors limiting New England cottontail populations at the edge of their range in New York State. Here, canopy closure, heathlands, and invasive shrubs may also play a large role in providing habitat and mitigating the negative impacts of competition with the eastern cottontail. This document is meant to serve as a technical guide for managers working to restore or create New England cottontail habitat in the face of these challenges. Recent work suggests current management practices may be ineffective or even harmful when the impacts of invasive shrubs and eastern cottontails are not considered in forest management decision- making. These guidelines provide background information and updated recommendations derived from recent and ongoing research on New England cottontails for use in developing site specific forest management plans. While we use New York specific examples, many of these challenges we discuss, such as management of New England cottontails in the presence of eastern cottontails, are rapidly becoming a range-wide concern. The guidance outlined herein is adaptable to similar habitat in New England. Prepared by: Amanda Cheeseman PhD. and Jonathan Cohen PhD from the State University of New York College of Environmental Science and Forestry in partnership with the New York State Department of Environmental Conservation. -
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. -
(Trematoda; Cestoda; Nematoda) Geographic Records from Three Species of Owls (Strigiformes) in Southeastern Oklahoma Chris T
92 New Ectoparasite (Diptera; Phthiraptera) and Helminth (Trematoda; Cestoda; Nematoda) Geographic Records from Three Species of Owls (Strigiformes) in Southeastern Oklahoma Chris T. McAllister Science and Mathematics Division, Eastern Oklahoma State College, Idabel, OK 74745 John M. Kinsella HelmWest Laboratory, 2108 Hilda Avenue, Missoula, MT 59801 Lance A. Durden Department of Biology, Georgia Southern University, Statesboro, GA 30458 Will K. Reeves Colorado State University, C. P. Gillette Museum of Arthropod Diversity, Fort Collins, CO 80521 Abstract: We are just now beginning to learn about the ectoparasites and helminth parasites of some owls of Oklahoma. Some recent contributions from our lab have attempted to help fill a previous void in that information. Here, we report, four taxa of ectoparasites and five helminth parasites from three species of owls in Oklahoma. They include two species of chewing lice (Strigiphilus syrnii and Kurodeia magna), two species of hippoboscid flies (Icosta americana and Ornithoica vicina), a trematode (Strigea elegans) and a cestode (Paruterina candelabraria) from barred owls (Strix varia), and three nematodes, Porrocaecum depressum from an eastern screech owl (Megascops asio), Capillaria sp. eggs from S. varia, and Capillaria tenuissima from a great horned owl (Bubo virginianus). With the exception of Capillaria sp. eggs and I. americana, all represent new state records for Oklahoma and extend our knowledge of the parasitic biota of owls of the state. to opportunistically examine raptors from the Introduction state and document new geographic records for their parasites in Oklahoma. Over 455 species of birds have been reported Methods from Oklahoma and several are species of raptors or birds of prey that make up an important Between January 2018 and September 2019, portion of the avian fauna of the state (Sutton three owls were found dead on the road in 1967; Baumgartner and Baumgartner 1992). -
Melo-Ferreira J, Lemos De Matos A, Areal H, Lissovski A, Carneiro M, Esteves PJ (2015) The
1 This is the Accepted version of the following article: 2 Melo-Ferreira J, Lemos de Matos A, Areal H, Lissovski A, Carneiro M, Esteves PJ (2015) The 3 phylogeny of pikas (Ochotona) inferred from a multilocus coalescent approach. Molecular 4 Phylogenetics and Evolution 84, 240-244. 5 The original publication can be found here: 6 https://www.sciencedirect.com/science/article/pii/S1055790315000081 7 8 The phylogeny of pikas (Ochotona) inferred from a multilocus coalescent approach 9 10 José Melo-Ferreiraa,*, Ana Lemos de Matosa,b, Helena Areala,b, Andrey A. Lissovskyc, Miguel 11 Carneiroa, Pedro J. Estevesa,d 12 13 aCIBIO, Centro de Investigação em Biodiversidade e Recursos Genéticos, Universidade do Porto, 14 InBIO, Laboratório Associado, Campus Agrário de Vairão, 4485-661 Vairão, Portugal 15 bDepartamento de Biologia, Faculdade de Ciências, Universidade do Porto, 4099-002 Porto, 16 Portugal 17 cZoological Museum of Moscow State University, B. Nikitskaya, 6, Moscow 125009, Russia 18 dCITS, Centro de Investigação em Tecnologias da Saúde, IPSN, CESPU, Gandra, Portugal 19 20 *Corresponding author: José Melo-Ferreira. CIBIO, Centro de Investigação em Biodiversidade e provided by Repositório Aberto da Universidade do Porto View metadata, citation and similar papers at core.ac.uk CORE brought to you by 21 Recursos Genéticos, Universidade do Porto, InBIO Laboratório Associado, Campus Agrário de 22 Vairão, 4485-661 Vairão. Phone: +351 252660411. E-mail: [email protected]. 23 1 1 Abstract 2 3 The clarification of the systematics of pikas (genus Ochotona) has been hindered by largely 4 overlapping morphological characters among species and the lack of a comprehensive molecular 5 phylogeny. -
Wildlife in Your Young Forest.Pdf
WILDLIFE IN YOUR Young Forest 1 More Wildlife in Your Woods CREATE YOUNG FOREST AND ENJOY THE WILDLIFE IT ATTRACTS WHEN TO EXPECT DIFFERENT ANIMALS his guide presents some of the wildlife you may used to describe this dense, food-rich habitat are thickets, T see using your young forest as it grows following a shrublands, and early successional habitat. timber harvest or other management practice. As development has covered many acres, and as young The following lists focus on areas inhabited by the woodlands have matured to become older forest, the New England cottontail (Sylvilagus transitionalis), a rare amount of young forest available to wildlife has dwindled. native rabbit that lives in parts of New York east of the Having diverse wildlife requires having diverse habitats on Hudson River, and in parts of Connecticut, Rhode Island, the land, including some young forest. Massachusetts, southern New Hampshire, and southern Maine. In this region, conservationists and landowners In nature, young forest is created by floods, wildfires, storms, are carrying out projects to create the young forest and and beavers’ dam-building and feeding. To protect lives and shrubland that New England cottontails need to survive. property, we suppress floods, fires, and beaver activities. Such projects also help many other kinds of wildlife that Fortunately, we can use habitat management practices, use the same habitat. such as timber harvests, to mimic natural disturbance events and grow young forest in places where it will do the most Young forest provides abundant food and cover for insects, good. These habitat projects boost the amount of food reptiles, amphibians, birds, and mammals.