Nocturnal Rodents
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Cross-Transmission Studies with Eimeria Arizonensis-Like Oocysts
University of Nebraska - Lincoln DigitalCommons@University of Nebraska - Lincoln Faculty Publications from the Harold W. Manter Laboratory of Parasitology Parasitology, Harold W. Manter Laboratory of 6-1992 Cross-Transmission Studies with Eimeria arizonensis-like Oocysts (Apicomplexa) in New World Rodents of the Genera Baiomys, Neotoma, Onychomys, Peromyscus, and Reithrodontomys (Muridae) Steve J. Upton Kansas State University Chris T. McAllister Department of Veterans Affairs Medical Cente Dianne B. Brillhart Kansas State University Donald W. Duszynski University of New Mexico, [email protected] Constance D. Wash University of New Mexico Follow this and additional works at: https://digitalcommons.unl.edu/parasitologyfacpubs Part of the Parasitology Commons Upton, Steve J.; McAllister, Chris T.; Brillhart, Dianne B.; Duszynski, Donald W.; and Wash, Constance D., "Cross-Transmission Studies with Eimeria arizonensis-like Oocysts (Apicomplexa) in New World Rodents of the Genera Baiomys, Neotoma, Onychomys, Peromyscus, and Reithrodontomys (Muridae)" (1992). Faculty Publications from the Harold W. Manter Laboratory of Parasitology. 184. https://digitalcommons.unl.edu/parasitologyfacpubs/184 This Article is brought to you for free and open access by the Parasitology, Harold W. Manter Laboratory of at DigitalCommons@University of Nebraska - Lincoln. It has been accepted for inclusion in Faculty Publications from the Harold W. Manter Laboratory of Parasitology by an authorized administrator of DigitalCommons@University of Nebraska - Lincoln. J. Parasitol., 78(3), 1992, p. 406-413 ? American Society of Parasitologists 1992 CROSS-TRANSMISSIONSTUDIES WITH EIMERIAARIZONENSIS-LIKE OOCYSTS (APICOMPLEXA) IN NEWWORLD RODENTS OF THEGENERA BAIOMYS, NEOTOMA, ONYCHOMYS,PEROMYSCUS, AND REITHRODONTOMYS(MURIDAE) Steve J. Upton, Chris T. McAllister*,Dianne B. Brillhart,Donald W. Duszynskit, and Constance D. -
Socioeconomic and Ecological Aspects of Field Rat Control in Tropical and Subtropical Countries Bans Kurylas
SOCIOECONOMIC AND ECOLOGICAL ASPECTS OF FIELD RAT CONTROL IN TROPICAL AND SUBTROPICAL COUNTRIES BANS KURYLAS. Thai-German Rodent Control Project. German Agency for Technical Cooperation (GTZ), P.O. Box 9-34, Bangkok. Thailand. ABSTRACT: The vital question. as to the cause of the pennanent increase in field rat populations throughout most tropical and subtropical areas. has been the subject of researchers and fielcM!en during the past years, in the hope of finding an answer to this problem. Man has made his way through history wherein he was gradually able to renounce nature and establish his own man-made cultural frame. Unlike other marrmals. man has no natural instincts to guide him through life. Brain and spirit have to compensate for lack of. physical capabilities and instincts. Man was forced to change his natural surroundings in order to serve his special and ever-growing needs . Survival meant not only using nature but more so changing it in order to develop his culture. The field rat has become man's "cultural treader"! Myomorpha is the largest suborder of the Order Rodentia. Of the 1700 rodents known to man. more than 1100 belong to this group. The greater part of the Myomorpha species are found within two families, which are Cricetidae with about 567 species and Muridae with about 475 species. Most of these rodents live either in trees or under the ground. They rarely collide with man's interest. Only a few rodent species have become "field rats" and seem to dwell in and utilize man's cultural steppe. Some species have even become cosmopolitan and are found in Europe. -
Body Size and Biomass Distributions of Carrion Visiting Beetles: Do Cities Host Smaller Species?
Ecol Res (2008) 23: 241–248 DOI 10.1007/s11284-007-0369-9 ORIGINAL ARTICLE Werner Ulrich Æ Karol Komosin´ski Æ Marcin Zalewski Body size and biomass distributions of carrion visiting beetles: do cities host smaller species? Received: 15 November 2006 / Accepted: 14 February 2007 / Published online: 28 March 2007 Ó The Ecological Society of Japan 2007 Abstract The question how animal body size changes Introduction along urban–rural gradients has received much attention from carabidologists, who noticed that cities harbour Animal and plant body size is correlated with many smaller species than natural sites. For Carabidae this aspects of life history traits and species interactions pattern is frequently connected with increasing distur- (dispersal, reproduction, energy intake, competition; bance regimes towards cities, which favour smaller Brown et al. 2004; Brose et al. 2006). Therefore, species winged species of higher dispersal ability. However, body size distributions (here understood as the fre- whether changes in body size distributions can be gen- quency distribution of log body size classes, SSDs) are eralised and whether common patterns exist are largely often used to infer patterns of species assembly and unknown. Here we report on body size distributions of energy use (Peters 1983; Calder 1984; Holling 1992; carcass-visiting beetles along an urban–rural gradient in Gotelli and Graves 1996; Etienne and Olff 2004; Ulrich northern Poland. Based on samplings of 58 necrophages 2005a, 2006). and 43 predatory beetle species, mainly of the families Many of the studies on local SSDs focused on the Catopidae, Silphidae, and Staphylinidae, we found number of modes and the shape. -
Classification of Mammals 61
© Jones & Bartlett Learning, LLC © Jones & Bartlett Learning, LLC NOT FORCHAPTER SALE OR DISTRIBUTION NOT FOR SALE OR DISTRIBUTION Classification © Jones & Bartlett Learning, LLC © Jones & Bartlett Learning, LLC 4 NOT FORof SALE MammalsOR DISTRIBUTION NOT FOR SALE OR DISTRIBUTION © Jones & Bartlett Learning, LLC © Jones & Bartlett Learning, LLC NOT FOR SALE OR DISTRIBUTION NOT FOR SALE OR DISTRIBUTION © Jones & Bartlett Learning, LLC © Jones & Bartlett Learning, LLC NOT FOR SALE OR DISTRIBUTION NOT FOR SALE OR DISTRIBUTION © Jones & Bartlett Learning, LLC © Jones & Bartlett Learning, LLC NOT FOR SALE OR DISTRIBUTION NOT FOR SALE OR DISTRIBUTION © Jones & Bartlett Learning, LLC © Jones & Bartlett Learning, LLC NOT FOR SALE OR DISTRIBUTION NOT FOR SALE OR DISTRIBUTION © Jones & Bartlett Learning, LLC © Jones & Bartlett Learning, LLC NOT FOR SALE OR DISTRIBUTION NOT FOR SALE OR DISTRIBUTION © Jones & Bartlett Learning, LLC © Jones & Bartlett Learning, LLC NOT FOR SALE OR DISTRIBUTION NOT FOR SALE OR DISTRIBUTION © Jones & Bartlett Learning, LLC © Jones & Bartlett Learning, LLC NOT FOR SALE OR DISTRIBUTION NOT FOR SALE OR DISTRIBUTION © Jones & Bartlett Learning, LLC © Jones & Bartlett Learning, LLC NOT FOR SALE OR DISTRIBUTION NOT FOR SALE OR DISTRIBUTION © Jones & Bartlett Learning, LLC. NOT FOR SALE OR DISTRIBUTION. 2ND PAGES 9781284032093_CH04_0060.indd 60 8/28/13 12:08 PM CHAPTER 4: Classification of Mammals 61 © Jones Despite& Bartlett their Learning,remarkable success, LLC mammals are much less© Jones stress & onBartlett the taxonomic Learning, aspect LLCof mammalogy, but rather as diverse than are most invertebrate groups. This is probably an attempt to provide students with sufficient information NOT FOR SALE OR DISTRIBUTION NOT FORattributable SALE OR to theirDISTRIBUTION far greater individual size, to the high on the various kinds of mammals to make the subsequent energy requirements of endothermy, and thus to the inabil- discussions of mammalian biology meaningful. -
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. -
Body Size, Not Phylogenetic Relationship Or Residency, Drives Interspecific Dominance in a Little Pocket Mouse Community
Animal Behaviour 137 (2018) 197e204 Contents lists available at ScienceDirect Animal Behaviour journal homepage: www.elsevier.com/locate/anbehav Body size, not phylogenetic relationship or residency, drives interspecific dominance in a little pocket mouse community * Rachel Y. Chock a, , Debra M. Shier a, b, Gregory F. Grether a a Department of Ecology & Evolutionary Biology, University of California, Los Angeles, CA, U.S.A. b Recovery Ecology, San Diego Zoo Institute for Conservation Research, Escondido, CA, U.S.A. article info The role of interspecific aggression in structuring ecological communities can be important to consider Article history: when reintroducing endangered species to areas of their historic range that are occupied by competitors. Received 6 September 2017 We sought to determine which species is the most serious interference competitor of the endangered Initial acceptance 6 November 2017 Pacific pocket mouse, Perognathus longimembris pacificus, and more generally, whether interspecific Final acceptance 1 December 2017 aggression in rodents is predicted by body size, residency status or phylogenetic relatedness. We carried out simulated territory intrusion experiments between P. longimembris and four sympatric species of MS. number: A17-00719 rodents (Chaetodipus fallax, Dipodomys simulans, Peromyscus maniculatus, Reithrodontomys megalotis)ina field enclosure in southern California sage scrub habitat. We found that body size asymmetries strongly Keywords: predicted dominance, regardless of phylogenetic relatedness or the residency status of the individuals. aggression The largest species, D. simulans, was the most dominant while the smallest species, R. megalotis, was the dominance least dominant to P. longimembris. Furthermore, P. longimembris actively avoided encounters with all interference competition Perognathus longimembris species, except R. -
Plant and Rodent Communities of Organ Pipe Cactus National Monument
Plant and rodent communities of Organ Pipe Cactus National Monument Item Type text; Thesis-Reproduction (electronic) Authors Warren, Peter Lynd Publisher The University of Arizona. Rights Copyright © is held by the author. Digital access to this material is made possible by the University Libraries, University of Arizona. Further transmission, reproduction or presentation (such as public display or performance) of protected items is prohibited except with permission of the author. Download date 29/09/2021 16:51:51 Link to Item http://hdl.handle.net/10150/566520 PLANT AND RODENT COMMUNITIES OF ORGAN PIPE CACTUS NATIONAL.MONUMENT by Peter Lynd Warren A Thesis Submitted to the Faculty of the DEPARTMENT OF ECOLOGY AND EVOLUTIONARY BIOLOGY In Partial Fulfillment of the Requirements For the Degree of MASTER OF SCIENCE In the Graduate College THE UNIVERSITY OF ARIZONA 1 9 7 9 STATEMENT BY AUTHOR This thesis has been submitted in partial fulfillment of re quirements for an advanced degree at The University of Arizona and is deposited in the University Library to be made available to borrowers under rules of the Library. Brief quotations from this thesis are allowable without special permission, provided that accurate acknowledgment of source is made. Requests for permission for extended quotation from or reproduction of this manuscript in whole or in part may be granted by the head of the major department or the Dean of the Graduate College when in his judg ment the proposed use of the material is in the interests of scholar ship. In all other instances, however, permission must be obtained from the author. -
Fisheries in Large Marine Ecosystems: Descriptions and Diagnoses
Fisheries in Large Marine Ecosystems: Descriptions and Diagnoses D. Pauly, J. Alder, S. Booth, W.W.L. Cheung, V. Christensen, C. Close, U.R. Sumaila, W. Swartz, A. Tavakolie, R. Watson, L. Wood and D. Zeller Abstract We present a rationale for the description and diagnosis of fisheries at the level of Large Marine Ecosystems (LMEs), which is relatively new, and encompasses a series of concepts and indicators different from those typically used to describe fisheries at the stock level. We then document how catch data, which are usually available on a smaller scale, are mapped by the Sea Around Us Project (see www.seaaroundus.org) on a worldwide grid of half-degree lat.-long. cells. The time series of catches thus obtained for over 180,000 half-degree cells can be regrouped on any larger scale, here that of LMEs. This yields catch time series by species (groups) and LME, which began in 1950 when the FAO started collecting global fisheries statistics, and ends in 2004 with the last update of these datasets. The catch data by species, multiplied by ex-vessel price data and then summed, yield the value of the fishery for each LME, here presented as time series by higher (i.e., commercial) groups. Also, these catch data can be used to evaluate the primary production required (PPR) to sustain fisheries catches. PPR, when related to observed primary production, provides another index for assessing the impact of the countries fishing in LMEs. The mean trophic level of species caught by fisheries (or ‘Marine Trophic Index’) is also used, in conjunction with a related indicator, the Fishing-in-Balance Index (FiB), to assess changes in the species composition of the fisheries in LMEs. -
91 Table F-10 Golden Eagle REA Mitigation
91 Table F-10 Golden Eagle REA Mitigation: Extrapolation of the Relative Productivity of Electric Pole Retrofitting in 2011 Over the 30 Years Associated with the Average Life Cycle of Wind Energy Projects Table F-11 Golden Eagle REA Scaling: Mitigation Owed for a 5-Year Permitted Take of 25 Golden Eagles (5 Eagles Annually) (REA Step 16) Total Debit 485.74 PV bird-years for 5 years of Golden Eagle take ÷ Relative Productivity of Electric Pole Retrofitting ÷4.20 Avoided loss of PV bird-years per retrofitted pole = Mitigation owed =115.61 Poles to be retrofitted to achieve no net loss PV=Present Value 92 APPENDIX G COMPENSATORY MITIGATION CASE STUDY7: POWER POLE RETROFITTING TO COMPENSATE FOR TAKE OF GOLDEN EAGLES To offset projected and permitted take, retrofitting of non- Avian Power Line Interaction Committee (APLIC) compliant power poles has been selected by the Service as the initial focus of compensatory mitigation projects. Raptor electrocution is a known source of eagle mortality in the United States (Franson et al. 1995, Millsap et al. 2004, APLIC 2006, Lehman et al. 2007, Lehman et al. 2010). In particular, Golden Eagles are electrocuted more than any other raptor in North America; Lehman et al. (2007) noted Golden Eagles accounted for 50 – 93% of all reported mortalities of raptor electrocutions. Eagles often come into contact with non-APLIC compliant electric transmission poles. These poles are often responsible for the high incidence of eagle mortality, especially in open habitat devoid of natural perches. Specific utility poles and line spans in need of retrofit due to known mortalities of eagles and other large raptors will be reviewed by the Service and selected for retrofit based on criteria specified below. -
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. -
Dipodomys Ingens)
Species Status Assessment Report for the Giant Kangaroo Rat (Dipodomys ingens) Photo by Elizabeth Bainbridge Version 1.0 August 2020 Prepared by the U.S. Fish and Wildlife Service August 2020 GKR SSA Report – August 2020 EXECUTIVE SUMMARY The U.S. Fish and Wildlife Service listed the giant kangaroo rat (Dipodomys ingens) as endangered under the Endangered Species Act in 1987 due to the threats of habitat loss and widespread rodenticide use (Service 1987, entire). The giant kangaroo rat is the largest species in the genus that contains all kangaroo rats. The giant kangaroo rat is found only in south-central California, on the western slopes of the San Joaquin Valley, the Carrizo and Elkhorn Plains, and the Cuyama Valley. The preferred habitat of the giant kangaroo rat is native, sloping annual grasslands with sparse vegetation (Grinnell, 1932; Williams, 1980). This report summarizes the results of a species status assessment (SSA) that the U. S. Fish and Wildlife Service (Service) completed for the giant kangaroo rat. To assess the species’ viability, we used the three conservation biology principles of resiliency, redundancy, and representation (together, the 3Rs). These principles rely on assessing the species at an individual, population, and species level to determine whether the species can persist into the future and avoid extinction by having multiple resilient populations distributed widely across its range. Giant kangaroo rats remain in fragmented habitat patches throughout their historical range. However, some areas where giant kangaroo rats once existed have not had documented occurrences for 30 years or more. The giant kangaroo rat is found in six geographic areas (units), representing the northern, middle, and southern portions of the range. -
Plants Are Producers! Draw the Different Producers Below
Name: ______________________________ The Unique Producer Every food chain begins with a producer. Plants are producers. They make their own food, which creates energy for them to grow, reproduce and survive. Being able to make their own food makes them unique; they are the only living things on Earth that can make their own source of food energy. Of course, they require sun, water and air to thrive. Given these three essential ingredients, you will have a healthy plant to begin the food chain. All plants are producers! Draw the different producers below. Apple Tree Rose Bushes Watermelon Grasses Plant Blueberry Flower Fern Daisy Bush List the three essential needs that every producer must have in order to live. © 2009 by Heather Motley Name: ______________________________ Producers can make their own food and energy, but consumers are different. Living things that have to hunt, gather and eat their food are called consumers. Consumers have to eat to gain energy or they will die. There are four types of consumers: omnivores, carnivores, herbivores and decomposers. Herbivores are living things that only eat plants to get the food and energy they need. Animals like whales, elephants, cows, pigs, rabbits, and horses are herbivores. Carnivores are living things that only eat meat. Animals like owls, tigers, sharks and cougars are carnivores. You would not catch a plant in these animals’ mouths. Then, we have the omnivores. Omnivores will eat both plants and animals to get energy. Whichever food source is abundant or available is what they will eat. Animals like the brown bear, dogs, turtles, raccoons and even some people are omnivores.