Northern Flying Squirrel, Galucomys Sabrinus
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Breeding Ecology of Barred Owls in the Central Appalachians
BREEDING ECOLOGY OF BARRED OWLS IN THE CENTRAL APPALACHIANS ABSTRACT- Eight pairs of breedingBarred Owls (Strix varia) in westernMaryland were studied. Nest site habitat was sampledand quantifiedusing a modificationof theJames and Shugart(1970) technique (see Titus and Mosher1981). Statisticalcomparison to 76 randomhabitat plots showed nest sites werb in moremature forest stands and closer to forest openings.There was no apparent association of nestsites with water. Cavity dimensions were compared statistically with 41 randomlyselected cavities. Except for cavityheight, there were no statistically significant differences between them. Smallmammals comprised 65.9% of the totalnumber of prey itemsrecorded, of which81.5% were members of the familiesCricetidae and Soricidae. Birds accounted for 14.6%of theprey items and crayfish and insects 19.5%. We also recordedan apparentinstance of juvenile cannibalism. Thirteennestlings were produced in 7 nests,averaging 1.9 young per nest.Only 2 of 5 nests,where the outcome was known,fledged young. The Barred Owl (Strix varia) is a common noc- STUDY AREA AND METHODS turnal raptor in forestsof the easternUnited States, The studywas conducted in Green Ridge State Forest (GRSF), though few detailedstudies of it havebeen pub- Allegany County, Maryland. It is within the Ridge and Valley lished.Most reportsare of singlenesting occurr- physiographicregion (Stoneand Matthews 1977), characterized by narrowmountain ridges oriented northeast to southwestsepa- encesand general observations(Bolles 1890; Carter rated by steepnarrow valleys(see Titus 1980). 1925; Henderson 1933; Robertson 1959; Brown About 74% of the countyand nearly all of GRSF is forested 1962; Caldwell 1972; Hamerstrom1973; Appel- Major foresttypes were describedby Brushet al. (1980).Predom- gate 1975; Soucy 1976; Bird and Wright 1977; inant tree speciesinclude white oak (Quercusalba), red oak (Q. -
Phylogenies of Flying Squirrels (Pteromyinae)
Journal of Mammalian Evolution, Vol. 9, No. 1/2, June 2002 (© 2002) Phylogenies of Flying Squirrels (Pteromyinae) Richard W. Thorington, Jr.,'''* Diane Pitassy,^ and Sharon A. Jansa^ The phylogeny of flying squirrels was assessed, based on analyses of 80 morphological characters. Three published hypotheses were tested with constraint trees and compared with trees based on heuristic searches, all using PAUP*. Analyses were conducted on unordered data, on ordered data (Wagner), and on ordered data using Dollo parsimony. Compared with trees based on heuristic searches, the McKenna (1962) constraint trees were consistently the longsst, requiring 8-11 more steps. The Mein (1970) constraint trees were shorter, requiring five to seven steps more than the unconstrained trees, and the Thorington and Darrow (20(X)) constraint trees were shorter yet, zero to one step longer than the corresponding unconstrained tree. In each of the constraint trees, some of the constrained nodes had poor character support. The heuristic trees provided best character support for three groups, but they did not resolve the basal trichotomy between a Glaucomys group of six genera, a Petaurista group of four genera, and a Trogopterus group of four genera. The inclusion of the small northern Eurasian flying squirrel, Pteminys, in the Peiaiiiisia group of giant South Asian flying squirrels is an unexpected hypothesis. Another novel hypothesis is the inclusion of the genus Aemmys, large animals from the Sunda Shelf, with the Trogopterus group of smaller "complex-toothed flying squirrels" from mainland Malaysia and southeast Asia. We explore the implications of this study for future analysis of molecular data and for past and future interpretations of the fossil record. -
Phylogenetic Relationships Among Six Flying Squirrel Gener,A Inferred from Mitochondrial Cytochrome B Gene Sequences
Phylogenetic Relationships among Six Flying Squirrel Gener,a Inferred from Mitochondrial Cytochrome b Gene Sequences 著者(英) Oshida Tatsuo, Lin Liang-Kong, Yanagisawa Hisashi, Endo Hideki, Masuda Ryuichi journal or Zoological Science publication title volume 17 number 4 page range 485-489 year 2000-05 URL http://id.nii.ac.jp/1588/00004215/ ZOOLOGICAL SCIENCE 17: 485–489 (2000) © 2000 Zoological Society of Japan Phylogenetic Relationships among Six Flying Squirrel Genera, Inferred from Mitochondrial Cytochrome b Gene Sequences Tatsuo Oshida1*, Liang-Kong Lin2, Hisashi Yanagawa3, Hideki Endo4 and Ryuichi Masuda1 1Chromosome Research Unit, Faculty of Science, Hokkaido University, Sapporo 060-0810, Japan 2Laboratory of Wildlife Ecology, Department of Biology, Tunghai University, Taichung 407, Taiwan 3Laboratory of Wildlife Ecology, Obihiro University and Veterinary Medicine, Obihiro 080-0843, Japan 4Department of Zoology, National Science Museum, Shinjuku-ku, Tokyo, 169-0073, Japan ABSTRACT—Petauristinae (flying squirrels) consists of 44 extant species in 14 recent genera, and their phylogenetic relationships and taxonomy are unsettled questions. We analyzed partial mitochondrial cyto- chrome b gene sequences (1,068 base pairs) to investigate the phylogenetic relationships among six flying squirrel genera (Belomys, Hylopetes, Petaurista, Petinomys, and Pteromys from Asia and Glaucomys from North America). Molecular phylogenetic trees, constructed by neighbor-joining and maximum likelihood methods, strongly indicated the closer relationship between Hylopetes and Petinomys with 100% bootstrap values. Belomys early split from other flying squirrels. Petaurista was closely related to Pteromys, and Glaucomys was most closely related to the cluster consisting of Hylopetes and Petinomys. The bootstrap values supporting branching at the deeper nodes were not always so high, suggesting the early radiation in the evolution of flying squirrels. -
Nest Box Utility for Arboreal Small Mammals in Vietnam's Tropical Forest Использование Дуплянок Для И
Russian J. Theriol. 10(2): 5964 © RUSSIAN JOURNAL OF THERIOLOGY, 2011 Nest box utility for arboreal small mammals in Vietnams tropical forest Ami Kato, Tatsuo Oshida, Son Truong Nguyen, Nghia Xuan Nguyen, Hao Van Luon, Tue Van Ha, Bich Quang Truong, Hideki Endo & Dang Xuan Nguyen ABSTRACT. To test nest box utility in a Southeast Asian tropical forest, we set 30 wooden nest boxes on trees in the Cuc Phuong National Park, Vietnam for a year. During the rainy season, we checked each nest box each month in the daytime. We expected that arboreal rodents might be more likely to use the nest boxes as shelter from the heavy rain. During dry season, we additionally checked each nest box every two months. We expected that nest boxes would be used as a shelter from the rain by small arboreal mammals, such as rats and flying squirrels in the rainy season more than in the dry season. During the rainy season, we found ants, bees, and birds mainly nested the nest boxes for reproduction: bees in April; ants from May to August; and birds from April to June. From the late rainy season to the dry season, arboreal small mammals mainly used nest boxes: rats from August to February and flying squirrel in December. Nest resource competition between birds and rodents may be minimal since they use cavities in different seasons. Also, unlike our expectation, it was preliminary suggested that arboreal small rodents would use more frequently nest box in the dry season than in the rainy season. KEY WORDS: flying squirrel, rat, rainy season, dry season, competition, nest resource, nest material. -
Tree Squirrels: Managing Habitat and Controlling Damage
■ ,VVXHG LQ IXUWKHUDQFH RI WKH &RRSHUDWLYH ([WHQVLRQ :RUN$FWV RI 0D\ DQG -XQH LQ FRRSHUDWLRQ ZLWK WKH 8QLWHG 6WDWHV 'HSDUWPHQWRI$JULFXOWXUH 'LUHFWRU&RRSHUDWLYH([WHQVLRQ8QLYHUVLW\RI0LVVRXUL&ROXPELD02 NATURAL ■ ■ ■ DQHTXDORSSRUWXQLW\$'$LQVWLWXWLRQ H[WHQVLRQPLVVRXULHGX RESOURCES Tree Squirrels: Managing Habitat and Controlling Damage issouri is home to three species of tree squirrels: the fox squirrel (Sciurus niger) and gray squirrel M(S. carolinensis), both popular game animals; and the southern flying squirrel Glaucomys( volans), the smallest of the tree squirrel species in the state. These squirrels provide relaxation and enjoyment for many Missourians who spend time observing or photo- graphing wildlife. They seldom pose problems in rural areas, but it is not unusual for them to become a nuisance in urban areas (Figure 1). Occasionally, fox or gray squirrels enter attics and chimneys and cause damage to electrical wiring, siding or insulation. Squirrels may cause damage to home gardens and ornamentals; sweet corn, tomatoes and other vegetables or flower bulbs; and newly planted seeds in urban gardens. Squirrels also can become a nuisance around bird feeders, frightening birds and scattering seeds. Figure 1. Squirrels can become a nuisance, especially in urban areas. Fox squirrels Gray squirrels normally prefer areas with more forest Fox squirrels are most common in urban areas and cover than fox squirrels. Forests dominated by oaks and open woodlots. They are the largest of the three species, hickories are prime habitats for gray squirrels. Gray averaging 19 to 29 inches from nose to tail and weighing 1 squirrels also prefer to spend more time in trees and do not to 3 pounds. -
Mammals of Vermont Vermont Natural Heritage Inventory Vermont Fish & Wildlife Department 22 March 2017
Mammals of Vermont Vermont Natural Heritage Inventory Vermont Fish & Wildlife Department 22 March 2017 The following is a list of mammal species known to regularly occur in Vermont. Historic species (not documented in Vermont in the last 25 years) are included if there is a reasonable expectation of their return. Not included are species that are extinct or extirpated from the state. The list is organized taxonomically to genus, then alphabetically within genus. Species not native to Vermont are indicated with an asterisk (*). Questions can be directed to the Vermont Natural Heritage Inventory, Vermont Fish & Wildlife Department, 1 National Life Drive, Montpelier, VT 05620-3702. (802) 241-3700. [email protected] State Global State Federal Scientific Name Common Name Rank Rank Status Status SGCN Didelphis virginiana Virginia Opossum S5 G5 Glaucomys sabrinus Northern Flying Squirrel S4 G5 SGCN Glaucomys volans Southern Flying Squirrel S5 G5 SGCN Marmota monax Woodchuck S5 G5 Sciurus carolinensis Eastern Gray Squirrel S5 G5 Tamias striatus Eastern Chipmunk S5 G5 Tamiasciurus hudsonicus Red Squirrel S5 G5 Castor canadensis American Beaver S5 G5 Napaeozapus insignis Woodland Jumping Mouse S5 G5 Zapus hudsonius Meadow Jumping Mouse S5 G5 Microtus chrotorrhinus Rock Vole S2 G4 SC SGCN Microtus pennsylvanicus Meadow Vole S5 G5 Microtus pinetorum Woodland Vole S3 G5 SGCN Myodes gapperi Southern Red-backed Vole S5 G5 Ondatra zibethicus Common Muskrat S5 G5 SGCN Peromyscus leucopus White-footed Deermouse S5 G5 Peromyscus maniculatus North -
Fifteen Years of Appalachian Northern Flying Squirrels
Herding Rats: Fifteen Years of Appalachian Northern Flying Squirrels Appalachian Northern VA-WV Northern Flying Squirrel Flying Squirrels Glaucomys sabrinus fuscus • Pleistocene relict Elkins, WV • G.s.coloratus inhabits high elevation forest islands in southern Appalachians; G.s.fuscus inhabits more connected landscape in Blacksburg, VA central Appalachians • Prefers red spruce or mixed red spruce-northern hardwood forests • Cavity nester Asheville, NC • Mycophagus Carolina Northern Flying Squirrel • Parasite-mediated Glaucomys sabrinus coloratus competition with G. volans Pre-exploitation forest structure similar to Pacific Northwest? Just 12 of us documented prior to 1980's in the Virginia’s The Blackwater Canyon: a private forest (forest management, surface mining, second-homes and wind energy) with public expectations. Snowshoe Resort Westvaco Research Forest Kumbrabow State Forest Canaan Valley NWR Kumbrabow SF and MeadWestvaco Ecosystem Research Forest Snowshoe Resort WV VA Glaucomys sabrinus fuscus captures through 2004 Ford, W.M., S.L. Stephenson, J.M. Menzel, D.R. Black and J.W. Edwards. 2004. Habitat characteristics of the endangered Virginia northern flying squirrel (Glaucomys sabrinus fuscus) in the Central Appalachian Mountains. American Midland Naturalist 152:430-438. Odom, R.H., W.M. Ford, J.W. Edwards, C. Stihler, and J.M. Menzel. 2001. Modeling Virginia northern flying squirrel habitat in the central Appalachians. Biological Conservation. 99:245-252. Menzel, J.M., W.M. Ford, J.W. Edwards and L.J. Ceperley. 2006. A habitat model for the Virginia northern flying squirrel (Glaucomys sabrinus fuscus) in the central Appalachian Mountains. USDA Forest Service Research Paper-NE-729. 10 p Den Tree Results •41 cavity and 18 drey nests •Yellow birch and Fraser’s magnolia chosen more than expected; Norway spruce, red spruce, American beech, black birch, red maple, sugar maple and black cherry used in proportion or less than expected. -
Carolina Northern Flying Squirrel Glaucomys Sabrinus
U.S. Fish & Wildlife Service Carolina northern flying squirrel Glaucomys sabrinus northern flying squirrels are relicts Range: Carolina northern flying of the last ice age. As the glaciers squirrels are found on high mountain retreated northward and temperatures peaks in southwest Virginia, western rose, remnant populations remained in North Carolina, and eastern Tennessee. the suitable habitat left behind on the Listing: Endangered, July 1, 1985. 50 high mountain tops along the ridges of FR 26999 27002 the Southern Appalachian Mountains. Critical habitat: None designated Northern flying squirrels principally feed on certain fungi and lichens, Threats: The limited and discontinuous though they do occasionally eat range of this sub-species in the some fruits and nuts. They’re active Southern Appalachians makes it year-round, but more so in the vulnerable to a number of natural warmer summer months. They nest and human-related impacts. Human in tree cavities in nests made almost impacts far outweigh natural threats exclusively of yellow birch bark, and include habitat destruction and where two to six young are born in fragmentation or other alterations early spring. Groups of squirrels associated with the clearing of forests, often occupy the same tree cavity, introduced exotic pests, recreational particularly in the colder winter and residential development, and months. pollution (heavy metals and acid rain). Habitat: Northern flying squirrels are Why should we be concerned about typically found in areas where northern the loss of species? Extinction is a hardwoods, such as yellow birch, are natural process that has been occurring Carolina northern flying squirrel, adjacent to the higher-elevation red since long before the appearance of Chris McGrath, NCWRC spruce-Fraser fir forest. -
Northern Flying Squirrel (Glaucomys Sabrinus) Species Guidance Family: Sciuridae – the Squirrels
Northern Flying Squirrel (Glaucomys sabrinus) Species Guidance Family: Sciuridae – the squirrels Species of Greatest Conservation Need (SGCN) State Status: SC/P (Special Concern/Fully Protected) State Rank: S3S4 Federal Status: None Global Rank: G5 Wildlife Action Plan Counties with documented locations Mean Risk Score: 3.2 of northern flying squirrels in Wildlife Action Plan Area of Wisconsin. Source: Natural Heritage Photo by Ryan Stephens Importance Score: 2 Inventory Database, April 2013. Species Information General Description: The northern flying squirrel and its sister species, the southern flying squirrel (Glaucomys volans), both occur in Wisconsin. The northern flying squirrel is slightly larger than the southern flying squirrel, but is small compared to other tree squirrels. Adult northern flying squirrels in the Great Lakes region weigh 70-130 g (2.5-4.6 oz) (Kurta 1995). Total length (including tail) ranges from 245-315 mm (10-12 in), tail length 110-150 mm (4.3-5.9 in), hindfoot length 35-40 mm (1.4-1.6 in), and ear height 18-26 mm (0.7-1.0 in) (Jackson 1961, Kurta 1995). Pelage (fur) is silky and usually cinnamon–colored, but can range from dark brown to red. Belly hair is white at the tips and gray at the base. The northern flying squirrel uses its patagium (loose flap of skin between the front and hind legs; Fig. 1) for gliding between trees. A cartilaginous projection called a styliform process extends from the wrist (Fig. 1) to widen the patagium and enhance its effect (Wells-Gosling and Heaney 1989). Similar Species: The flying squirrels can easily be distinguished from the other eight Wisconsin squirrels by the presence of a furry patagium (flap of skin) that runs from the wrist to the ankle, and also by a cartilaginous projection on the wrist called a styliform process. -
FLYING SQUIRRELS Southern Flying Squirrel: Glaucomys Volans Northern Flying Squirrel: Glaucomys Sabrinus
WILDLIFE IN CONNECTICUT INFORMATIONAL SERIES FLYING SQUIRRELS Southern flying squirrel: Glaucomys volans Northern flying squirrel: Glaucomys sabrinus Habitat: Mature deciduous or mixed deciduous/ Length: Southern flying squirrel, 8 to 10 inches. coniferous forests with an abundance of various nut- Northern flying squirrel, 9.8 to 11.5 inches. producing trees. Food: Acorns, nuts, seeds, berries, blossoms, mush- Weight: Southern flying squirrel, 1.8 to 2.5 ounces. rooms, moths, beetles, and small birds and their eggs. Northern flying squirrel, 2 to 4.4 ounces. Identification: Flying squirrels have soft, gray-brown fur summer. The young are born blind and helpless but on the back and sides, with white underparts, a flattened develop more quickly than other squirrels. By six weeks tail and large, dark eyes for night vision. The northern of age, they are able to forage on their own. Tree flying squirrel is slightly darker and redder than the cavities and even bird houses may be used as nesting southern flying squirrel. The loose folds of skin between sites. The nest may be lined with shredded bark, leaves, the front and hind legs of these squirrels enables them moss, feathers, and other materials. to “fly;” they actually glide through the air on the History in Connecticut: The southern squirrel is found stretched surface of this loose skin. throughout Connecticut, but the northern flying squirrel's Range: The southern flying squirrel is found from range includes only the higher elevations of the north- southern Canada south to southern Florida, west to western part of the state. Due to their nocturnal nature, Minnesota and eastern Texas. -
SAN BERNARDINO FLYING SQUIRREL (Glaucomys Sabrinus Californicus) AS THREATENED OR ENDANGERED UNDER the UNITED STATES ENDANGERED SPECIES ACT
BEFORE THE SECRETARY OF INTERIOR PETITION TO LIST THE SAN BERNARDINO FLYING SQUIRREL (Glaucomys sabrinus californicus) AS THREATENED OR ENDANGERED UNDER THE UNITED STATES ENDANGERED SPECIES ACT Northern flying squirrel, Dr. Lloyd Glenn Ingles © California Academy of Sciences CENTER FOR BIOLOGICAL DIVERSITY, PETITIONER AUGUST 24, 2010 NOTICE OF PETITION Ken Salazar, Secretary of the Interior Ren Lohoefener, Regional Director U.S. Department of the Interior U.S. Fish and Wildlife Service Region 8 1849 C Street, N.W. 2800 Cottage Way, W-2606 Washington, DC 20240 Sacramento, CA 95825 Phone: (202) 208-3100 Phone: (503) 231-6118 [email protected] [email protected] Rowan Gould, Acting Director U.S. Fish and Wildlife Service 1849 C Street, NW, Mail Stop 3012 Washington, D.C. 20240 Phone: (202) 208-4717 Fax: (202) 208-6965 [email protected] PETITIONER Shaye Wolf, Ph.D. Center for Biological Diversity 351 California Street, Suite 600 San Francisco, CA 94104 office: (415) 632-5301 cell: (415) 385-5746 fax: (415) 436-9683 [email protected] __________________________ Date this 24th day of August, 2010 Pursuant to Section 4(b) of the Endangered Species Act (“ESA”), 16 U.S.C. §1533(b), Section 553(3) of the Administrative Procedures Act, 5 U.S.C. § 553(e), and 50 C.F.R. § 424.14(a), the Center for Biological Diversity hereby petitions the Secretary of the Interior, through the United States Fish and Wildlife Service (“USFWS”), to list the San Bernardino flying squirrel (Glaucomys sabrinus californicus) as a threatened or endangered species and to designate critical habitat to ensure its survival and recovery. -
Barred Owl Presentation
A Tale of Two Owls: New Challenges in Spotted Owl Conservation Lowell Diller Green Diamond Resource Company, Korbel, CA At listing (1990), primary threat to Northern Spotted Owl was loss and fragmentation of habitat Northwest Forest Plan – 1994 18.5 million acres in various reserves Range-wide threat of habitat loss still exists, but it has been stabilized in the last two decades. ! Crescent City 1992 ! Crescent City 2002 ! Crescent City 2012 ! Crescent City 2022 On Green the Del Norte Co. Del Norte Co. Del Norte Co. Del Norte Co. Orick Orick Orick Orick amount of high ! ! ! ! quality habitat is projected to Willow Creek Willow Creek Willow Creek Willow Creek ! ! ! ! Korbel Korbel Korbel Korbel ! ! ! ! be increasing. Eureka Eureka Eureka Eureka ! ! ! ! ! ! Humboldt Co. ! Humboldt Co. ! Humboldt Co. Humboldt Co. Fortuna Fortuna Fortuna Fortuna Relative Distribution 0 10 20 Kilometers of Habitat Lambda High Medium Low © Do NSO numbers reflect habitat 2012: 83% decline trends? - Washington D. Herter: “hardly any left” Realized rate of population change - WA 2012: 3 pairs & 8 singles remain Forsman et al. 2011 Trends in NSO, Olympic National Park Location and occupancy status of 52 monitored spotted owl territories in Olympic National Park, 2013. Black circles are spotted owl pairs, half-filled circles are single owls and white circles are monitored sites with no response. Shaded area within the park boundary is high elevation non-habitat. (Gremel 2013) Oregon trends in NSO numbers – all areas with major declines since last meta-analysis California trends in NSO 2012: ~50% decline numbers based on demographic study areas 2012: >50% decline A new threat in the form of a distant cousin from the east • BO separated from NSO for millions for years • Closest relative to the BO are the Neotropical “Ciccaba” (now Strix) owls (G.