The Striped Skunk Mephitis Mephitis Is About the Size of a Cat, but Has a Stout Body, a Rather Small Head, Short Legs, and a Bushy Tail
Total Page:16
File Type:pdf, Size:1020Kb
Load more
Recommended publications
-
Striped Skunk Mephitis Mephitis
Striped Skunk Mephitis mephitis Other common names None Introduction Striped skunks are highly recognizable for their distinctive coloring and their ability to spray an extremely foul smelling substance when they feel threatened. Some folks may also recognize them as the inspiration for the Looney Tunes character Pepé le Pew. There are 11 different species in the skunk family, with 5 species residing throughout the United States, but only the striped skunk can be found in New York. Physical Description and Anatomy Striped skunks are about the size of an average domestic cat. Adults can Pepé le Pew weigh anywhere between 2 – 12 lbs (0.9 – 5.4 kg), and are 18 – 32 inches (45.7 – 81.3 cm) long, with the tail making up 7 – 11 inches (17.8 – 27.9 cm) of that length. They have a stout body, short legs, and a long, bushy tail. Each foot is equipped with five strong claws that are used for digging. The bold striping pattern of the glossy black and white fur is highly variable. This coloration is designed to serve as a warning to other species not to bother it, or they will suffer the consequences. Generally, the top of the head is white, which splits into two stripes of white down the back, divided by a stripe of black. The lower parts are black as well. Variations may result in individuals that are all white above and all black below, some other combination of stripes and patches, or almost solid white or black. Skunks have such bold coloration because they Picture showing variation in color patterns of striped skunk. -
2021 Fur Harvester Digest 3 SEASON DATES and BAG LIMITS
2021 Michigan Fur Harvester Digest RAP (Report All Poaching): Call or Text (800) 292-7800 Michigan.gov/Trapping Table of Contents Furbearer Management ...................................................................3 Season Dates and Bag Limits ..........................................................4 License Types and Fees ....................................................................6 License Types and Fees by Age .......................................................6 Purchasing a License .......................................................................6 Apprentice & Youth Hunting .............................................................9 Fur Harvester License .....................................................................10 Kill Tags, Registration, and Incidental Catch .................................11 When and Where to Hunt/Trap ...................................................... 14 Hunting Hours and Zone Boundaries .............................................14 Hunting and Trapping on Public Land ............................................18 Safety Zones, Right-of-Ways, Waterways .......................................20 Hunting and Trapping on Private Land ...........................................20 Equipment and Fur Harvester Rules ............................................. 21 Use of Bait When Hunting and Trapping ........................................21 Hunting with Dogs ...........................................................................21 Equipment Regulations ...................................................................22 -
Placental Haemophagous Organs in the Procyonidae and Mustelidae
PLACENTAL HAEMOPHAGOUS ORGANS IN THE PROCYONIDAE AND MUSTELIDAE R. F. S. CREED and J. D. BIGGERS Royal Veterinary College, London, N.W. 1, and the King Ranch Laboratory oj Reproductive Physiology, School of Veterinary Medicine, University of Pennsylvania, Philadelphia, U.S.A. {Received 9th January 1964) Summary. A description is given of some of the gross anatomical characteristics of the placenta of representatives of five carnivore species of the families Procyonidae and Mustelidae. Emphasis is laid on the occurrence of well-defined haemophagocytic structures in these placen- tae, which have not, hitherto, been investigated. INTRODUCTION Recently, the name haemophagous organ was proposed for a particular structure found in the raccoon {Procyon lotor lotor L.) placenta (Biggers & Creed, 1962). This highly vascular sac-like structure, which hangs into the allantoic cavity, is of macroscopic dimensions and emerges from a central antimesometrial region of the placental annulus in this procyonid carnivore (Pi. 1, Fig. 1). It increases in size and complexity until about two-thirds to three-quarters of the gestation period has elapsed, after which it regresses. Morphologically it is quite distinct from the rest of the placenta which is labyrinthine, and histo¬ logical examination shows it to be made up of a series of branching and anasto¬ mosing lamellae which consist of a thin core of foetal mesenchyme, containing foetal capillaries, lined on either side by tall foetal columnar epithelial cells. Interlamellar spaces are filled with maternal blood which gains access from the maternal side at the base of the haemophagous organ, and bathes the foetal columnar epithelium. The cells of this epithelium bear every indication of being phagocytic and appear to be concerned essentially with the ingestion of maternal blood corpuscles (Biggers & Creed, 1962; Creed & Biggers, 1963a, b). -
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. -
Black Bears in New York State
eavy-set, formidable-looking animals, wild black bears are one of New York State’s largest land mammals. Though frequently thought of as aggressive and menacing, they are ordinarily very shy, elusive, secretive creatures. In fact, although common in most of the state, black bears try to avoid people and so are seldom seen by many. DESCRIPTION FOOD AND FAMILY LIFE Native to North America, black bears (Ursus americanus) New York’s largest carnivore, black bears are primarily occur in Alaska, Canada, northern Mexico and most of the vegetarians, eating an amazing amount of small items such lower forty-eight states. They prefer wooded areas, occurring as succulent plants (like skunk cabbage), grasses, sedges, in and around mature forests. Black bears also do well in clover, insects (especially ants and bees), berries, fruits, somewhat open and developed areas as long as adequate nuts, mast (acorns and beechnuts), and plant roots. cover and an abundance of food are available. They are However, bears are opportunists and will eat whatever is intelligent and curious and spend a great deal of time readily available, including amphibians, reptiles, small exploring for food. Solitary animals, they usually live alone, mammals, fish, carrion and garbage. In addition, they will except for females with cubs and in feeding areas with an also avail themselves of human foods (almost everything abundance of food. Adult bears have large home ranges, from barbecued chicken to freeze dried meals and trail with males traveling up to 100 square miles, and females mix), bird seed (especially sunflower seeds), suet, pet food, traveling 25 to 50 square miles. -
First Documentation of Scent-Marking Behaviors in Striped Skunks (Mephitis Mephitis)
Mammal Research (2021) 66:399–404 https://doi.org/10.1007/s13364-021-00565-8 ORIGINAL PAPER First documentation of scent-marking behaviors in striped skunks (Mephitis mephitis) Kathrina Jackson1 & Christopher C. Wilmers 2 & Heiko U. Wittmer 3 & Maximilian L. Allen4 Received: 9 October 2020 /Accepted: 16 March 2021 / Published online: 11 April 2021 # Mammal Research Institute, Polish Academy of Sciences, Bialowieza, Poland 2021 Abstract Communication behaviors play a critical role in both an individual’s fitness as well as the viability of populations. Solitary animals use chemical communication (i.e., scent marking) to locate mates and defend their territory to increase their own fitness. Previous research has suggested that striped skunks (Mephitis mephitis) do not perform scent-marking behaviors, despite being best known for using odor as chemical defense. We used video camera traps to document behaviors exhibited by striped skunks at a remote site in coastal California between January 2012 and April 2015. Our camera traps captured a total of 71 visits by striped skunks, the majority of which (73%) included a striped skunk exhibiting scent-marking behaviors. Overall, we documented 8 different scent-marking behaviors. The most frequent behaviors we documented were cheek rubbing (45.1%), investigating (40.8%), and claw marking (35.2%). The behaviors exhibited for the longest durations on average were grooming (x =34.4s) and investigating (x = 21.2 s). Although previous research suggested that striped skunks do not scent mark, we documented that at least some populations do and our findings suggest that certain sites are used for communication via scent marking. -
Brown Bear (Ursus Arctos) John Schoen and Scott Gende Images by John Schoen
Brown Bear (Ursus arctos) John Schoen and Scott Gende images by John Schoen Two hundred years ago, brown (also known as grizzly) bears were abundant and widely distributed across western North America from the Mississippi River to the Pacific and from northern Mexico to the Arctic (Trevino and Jonkel 1986). Following settlement of the west, brown bear populations south of Canada declined significantly and now occupy only a fraction of their original range, where the brown bear has been listed as threatened since 1975 (Servheen 1989, 1990). Today, Alaska remains the last stronghold in North America for this adaptable, large omnivore (Miller and Schoen 1999) (Fig 1). Brown bears are indigenous to Southeastern Alaska (Southeast), and on the northern islands they occur in some of the highest-density FIG 1. Brown bears occur throughout much of southern populations on earth (Schoen and Beier 1990, Miller et coastal Alaska where they are closely associated with salmon spawning streams. Although brown bears and grizzly bears al. 1997). are the same species, northern and interior populations are The brown bear in Southeast is highly valued by commonly called grizzlies while southern coastal populations big game hunters, bear viewers, and general wildlife are referred to as brown bears. Because of the availability of abundant, high-quality food (e.g. salmon), brown bears enthusiasts. Hiking up a fish stream on the northern are generally much larger, occur at high densities, and have islands of Admiralty, Baranof, or Chichagof during late smaller home ranges than grizzly bears. summer reveals a network of deeply rutted bear trails winding through tunnels of devil’s club (Oplopanx (Klein 1965, MacDonald and Cook 1999) (Fig 2). -
Controlled Animals
Environment and Sustainable Resource Development Fish and Wildlife Policy Division Controlled Animals Wildlife Regulation, Schedule 5, Part 1-4: Controlled Animals Subject to the Wildlife Act, a person must not be in possession of a wildlife or controlled animal unless authorized by a permit to do so, the animal was lawfully acquired, was lawfully exported from a jurisdiction outside of Alberta and was lawfully imported into Alberta. NOTES: 1 Animals listed in this Schedule, as a general rule, are described in the left hand column by reference to common or descriptive names and in the right hand column by reference to scientific names. But, in the event of any conflict as to the kind of animals that are listed, a scientific name in the right hand column prevails over the corresponding common or descriptive name in the left hand column. 2 Also included in this Schedule is any animal that is the hybrid offspring resulting from the crossing, whether before or after the commencement of this Schedule, of 2 animals at least one of which is or was an animal of a kind that is a controlled animal by virtue of this Schedule. 3 This Schedule excludes all wildlife animals, and therefore if a wildlife animal would, but for this Note, be included in this Schedule, it is hereby excluded from being a controlled animal. Part 1 Mammals (Class Mammalia) 1. AMERICAN OPOSSUMS (Family Didelphidae) Virginia Opossum Didelphis virginiana 2. SHREWS (Family Soricidae) Long-tailed Shrews Genus Sorex Arboreal Brown-toothed Shrew Episoriculus macrurus North American Least Shrew Cryptotis parva Old World Water Shrews Genus Neomys Ussuri White-toothed Shrew Crocidura lasiura Greater White-toothed Shrew Crocidura russula Siberian Shrew Crocidura sibirica Piebald Shrew Diplomesodon pulchellum 3. -
Museum of Natural History
p m r- r-' ME FYF-11 - - T r r.- 1. 4,6*. of the FLORIDA MUSEUM OF NATURAL HISTORY THE COMPARATIVE ECOLOGY OF BOBCAT, BLACK BEAR, AND FLORIDA PANTHER IN SOUTH FLORIDA David Steffen Maehr Volume 40, No. 1, pf 1-176 1997 == 46 1ms 34 i " 4 '· 0?1~ I. Al' Ai: *'%, R' I.' I / Em/-.Ail-%- .1/9" . -_____- UNIVERSITY OF FLORIDA GAINESVILLE Numbers of the BULLETIN OF THE FLORIDA MUSEUM OF NATURAL HISTORY am published at irregular intervals Volumes contain about 300 pages and are not necessarily completed in any one calendar year. JOHN F. EISENBERG, EDITOR RICHARD FRANZ CO-EDIWR RHODA J. BRYANT, A£ANAGING EMOR Communications concerning purchase or exchange of the publications and all manuscripts should be addressed to: Managing Editor. Bulletin; Florida Museum of Natural Histoty, University of Florida P. O. Box 117800, Gainesville FL 32611-7800; US.A This journal is printed on recycled paper. ISSN: 0071-6154 CODEN: BF 5BAS Publication date: October 1, 1997 Price: $ 10.00 Frontispiece: Female Florida panther #32 treed by hounds in a laurel oak at the site of her first capture on the Florida Panther National Wildlife Refuge in central Collier County, 3 February 1989. Photograph by David S. Maehr. THE COMPARATIVE ECOLOGY OF BOBCAT, BLACK BEAR, AND FLORIDA PANTHER IN SOUTH FLORIDA David Steffen Maehri ABSTRACT Comparisons of food habits, habitat use, and movements revealed a low probability for competitive interactions among bobcat (Lynx ndia). Florida panther (Puma concotor cooi 1 and black bear (Urns amencanus) in South Florida. All three species preferred upland forests but ©onsumed different foods and utilized the landscape in ways that resulted in ecological separation. -
The 2008 IUCN Red Listings of the World's Small Carnivores
The 2008 IUCN red listings of the world’s small carnivores Jan SCHIPPER¹*, Michael HOFFMANN¹, J. W. DUCKWORTH² and James CONROY³ Abstract The global conservation status of all the world’s mammals was assessed for the 2008 IUCN Red List. Of the 165 species of small carni- vores recognised during the process, two are Extinct (EX), one is Critically Endangered (CR), ten are Endangered (EN), 22 Vulnerable (VU), ten Near Threatened (NT), 15 Data Deficient (DD) and 105 Least Concern. Thus, 22% of the species for which a category was assigned other than DD were assessed as threatened (i.e. CR, EN or VU), as against 25% for mammals as a whole. Among otters, seven (58%) of the 12 species for which a category was assigned were identified as threatened. This reflects their attachment to rivers and other waterbodies, and heavy trade-driven hunting. The IUCN Red List species accounts are living documents to be updated annually, and further information to refine listings is welcome. Keywords: conservation status, Critically Endangered, Data Deficient, Endangered, Extinct, global threat listing, Least Concern, Near Threatened, Vulnerable Introduction dae (skunks and stink-badgers; 12), Mustelidae (weasels, martens, otters, badgers and allies; 59), Nandiniidae (African Palm-civet The IUCN Red List of Threatened Species is the most authorita- Nandinia binotata; one), Prionodontidae ([Asian] linsangs; two), tive resource currently available on the conservation status of the Procyonidae (raccoons, coatis and allies; 14), and Viverridae (civ- world’s biodiversity. In recent years, the overall number of spe- ets, including oyans [= ‘African linsangs’]; 33). The data reported cies included on the IUCN Red List has grown rapidly, largely as on herein are freely and publicly available via the 2008 IUCN Red a result of ongoing global assessment initiatives that have helped List website (www.iucnredlist.org/mammals). -
PDF File Containing Table of Lengths and Thicknesses of Turtle Shells And
Source Species Common name length (cm) thickness (cm) L t TURTLES AMNH 1 Sternotherus odoratus common musk turtle 2.30 0.089 AMNH 2 Clemmys muhlenbergi bug turtle 3.80 0.069 AMNH 3 Chersina angulata Angulate tortoise 3.90 0.050 AMNH 4 Testudo carbonera 6.97 0.130 AMNH 5 Sternotherus oderatus 6.99 0.160 AMNH 6 Sternotherus oderatus 7.00 0.165 AMNH 7 Sternotherus oderatus 7.00 0.165 AMNH 8 Homopus areolatus Common padloper 7.95 0.100 AMNH 9 Homopus signatus Speckled tortoise 7.98 0.231 AMNH 10 Kinosternon subrabum steinochneri Florida mud turtle 8.90 0.178 AMNH 11 Sternotherus oderatus Common musk turtle 8.98 0.290 AMNH 12 Chelydra serpentina Snapping turtle 8.98 0.076 AMNH 13 Sternotherus oderatus 9.00 0.168 AMNH 14 Hardella thurgi Crowned River Turtle 9.04 0.263 AMNH 15 Clemmys muhlenbergii Bog turtle 9.09 0.231 AMNH 16 Kinosternon subrubrum The Eastern Mud Turtle 9.10 0.253 AMNH 17 Kinixys crosa hinged-back tortoise 9.34 0.160 AMNH 18 Peamobates oculifers 10.17 0.140 AMNH 19 Peammobates oculifera 10.27 0.140 AMNH 20 Kinixys spekii Speke's hinged tortoise 10.30 0.201 AMNH 21 Terrapene ornata ornate box turtle 10.30 0.406 AMNH 22 Terrapene ornata North American box turtle 10.76 0.257 AMNH 23 Geochelone radiata radiated tortoise (Madagascar) 10.80 0.155 AMNH 24 Malaclemys terrapin diamondback terrapin 11.40 0.295 AMNH 25 Malaclemys terrapin Diamondback terrapin 11.58 0.264 AMNH 26 Terrapene carolina eastern box turtle 11.80 0.259 AMNH 27 Chrysemys picta Painted turtle 12.21 0.267 AMNH 28 Chrysemys picta painted turtle 12.70 0.168 AMNH 29 -
A New Kinkajou from Mexico and a New Hooded Skunk from Central America by GEORGE G
PUBLISHED BY THE AMERICAN MUSEUM OF NATURAL HISTORY CENTRAL PARK WEST AT 79TH STREET, NEW YORK 24, N.Y. NUMBER 1830 MAY 3, 1957 A New Kinkajou from Mexico and a New Hooded Skunk from Central America BY GEORGE G. GOODWIN In a collection of mammals from northwestern Chiapas, Mexico, re- cently made by students of Walla Walla College under the supervision of Dr. Ernest S. Booth, there is a specimen of an unusually small kinkajou. The small size and long, thick, soft pelage of this specimen seem to warrant recognition by name of a geographical form inhabiting the highlands of northwestern Chiapas. A review of the Central American hooded skunks in the American Museum of Natural History collection shows that the specimens listed by J. A. Allen, 1908, 1910, from Nicaragua as Mephitis macroufa vittata differ sufficiently in cranial characters from named forms to be recognized as a distinct subspecies. At the time, Allen apparently based his diagnosis on measurements alone, without actually seeing typical specimens of. M. mn. vittata from southern Oaxaca. This new hooded skunk and the new kinkajou mentioned above are described below. Potos flavus boothi, new subspecies CHIAPAS KINKAJOU TYPE: A.M.N.H. No. 172183, skin and skull, adult female; Pueblo Nuevo, Solistahuacan, about 60 miles north of Tuxtla Gutierrez, Chiapas, Mexico. Altitude approximately 7000 feet; collectors, Percy Clifton and Brian S. Bull; February 8, 1956. The type skin is in first-class condition, and the skull is complete except for a break in the supraoccipital. GENERAL CHARACTERS: A small, golden brown kinkajou with rela- 2 AMERICAN MUSEUM NOVITATES NO.