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Mammals of the California Desert
MAMMALS OF THE CALIFORNIA DESERT William F. Laudenslayer, Jr. Karen Boyer Buckingham Theodore A. Rado INTRODUCTION I ,+! The desert lands of southern California (Figure 1) support a rich variety of wildlife, of which mammals comprise an important element. Of the 19 living orders of mammals known in the world i- *- loday, nine are represented in the California desert15. Ninety-seven mammal species are known to t ':i he in this area. The southwestern United States has a larger number of mammal subspecies than my other continental area of comparable size (Hall 1981). This high degree of subspeciation, which f I;, ; leads to the development of new species, seems to be due to the great variation in topography, , , elevation, temperature, soils, and isolation caused by natural barriers. The order Rodentia may be k., 2:' , considered the most successful of the mammalian taxa in the desert; it is represented by 48 species Lc - occupying a wide variety of habitats. Bats comprise the second largest contingent of species. Of the 97 mammal species, 48 are found throughout the desert; the remaining 49 occur peripherally, with many restricted to the bordering mountain ranges or the Colorado River Valley. Four of the 97 I ?$ are non-native, having been introduced into the California desert. These are the Virginia opossum, ' >% Rocky Mountain mule deer, horse, and burro. Table 1 lists the desert mammals and their range 1 ;>?-axurrence as well as their current status of endangerment as determined by the U.S. fish and $' Wildlife Service (USWS 1989, 1990) and the California Department of Fish and Game (Calif. -
Fleas, Hosts and Habitat: What Can We Predict About the Spread of Vector-Borne Zoonotic Diseases?
2010 Fleas, Hosts and Habitat: What can we predict about the spread of vector-borne zoonotic diseases? Ph.D. Dissertation Megan M. Friggens School of Forestry I I I \, l " FLEAS, HOSTS AND HABITAT: WHAT CAN WE PREDICT ABOUT THE SPREAD OF VECTOR-BORNE ZOONOTIC DISEASES? by Megan M. Friggens A Dissertation Submitted in Partial Fulfillment of the Requirements for the Degree of Doctor of Philosophy in Forest Science Northern Arizona University May 2010 ?Jii@~-~-u-_- Robert R. Parmenter, Ph. D. ~",l(*~ l.~ Paulette L. Ford, Ph. D. --=z:r-J'l1jU~ David M. Wagner, Ph. D. ABSTRACT FLEAS, HOSTS AND HABITAT: WHAT CAN WE PREDICT ABOUT THE SPREAD OF VECTOR-BORNE ZOONOTIC DISEASES? MEGAN M. FRIGGENS Vector-borne diseases of humans and wildlife are experiencing resurgence across the globe. I examine the dynamics of flea borne diseases through a comparative analysis of flea literature and analyses of field data collected from three sites in New Mexico: The Sevilleta National Wildlife Refuge, the Sandia Mountains and the Valles Caldera National Preserve (VCNP). My objectives were to use these analyses to better predict and manage for the spread of diseases such as plague (Yersinia pestis). To assess the impact of anthropogenic disturbance on flea communities, I compiled and analyzed data from 63 published empirical studies. Anthropogenic disturbance is associated with conditions conducive to increased transmission of flea-borne diseases. Most measures of flea infestation increased with increasing disturbance or peaked at intermediate levels of disturbance. Future trends of habitat and climate change will probably favor the spread of flea-borne disease. -
Complement Fixation Tests for Murine Typhus
ice under glass seal. The animals' brains were Complement Fixation Tests removed for tissue infectivity tests and were also stored on dry ice. Tests of the tissues of For Murine Typhus serologically reactive animals and pools of their fleas aided in evaluating the significance of low On Small Mammals titers. Blood samples were obtained by cardiac By RUTH KEATON, B.S. puncture soon after capture of the animals. BILLIE JO NASH, B.A. Serums were separated aseptically and were J. N. MURPHY, JR., M.A., M.S.P.H. kept at ice-box temperature until examination. J. V. IRONS, Sc.D. Serums were inactivated 30 minutes immedi- ately before testing at 56° C. Each serum was subjected to a quantitative complement tT HE IMPORTANCE of commensal rats fixation test employing endemic typhus rick- and their fleas in the epidemiology of en- ettsiae. A slight modification of the pro- demic typhus was well establislhed in 1931 (1,2). cedure described by Brigham and Bensgton Following Dyer's report (3) on the experi- (11) was used. The result was recorded as mental infection of the woodchuck, meadow reactive when a 3 + or greater reaction was ob- mouse, and whitefooted mouse with endemic tained with satisfactory controls at a 1: 20 or tvphus, Brigham (4, 5) indicated that many greater dilution of serum. species of rodents and other mammals were ap- When a serum was reactive, the correspond- parently susceptible to endemic typhus. Spar- ing brain suspension was emulsified and inocu- row (6) recovered a strain of endemic typhus lated individually into hamsters for evidence of rickettsiae in the house mouse (.Mus musodus), typhus. -
Paleontological Resources of the Upper and Middle San Pedro Valley
Paleontological Resources of the Upper and Middle San Pedro Valley Robert D. McCord Arizona Museum of Natural History Geological setting Regional extension causing block faulting – creation of the Basin and Range ~15Ma Poorly developed drainage results in lakes in valley bottom ?-3.4 Ma Drainage develops with flow to north, marshes, ponds and lakes significant from time to time Early Pleistocene Saint David Formation ? – 3.4 million lakes, few fossils Well developed paleomagnetic timeframe – a first for terrestrial sediments! Succession of faunas from ~3 to 1.5 Ma Blancan to ? Irvingtonian NALMA Plants diatoms charophytes Equisetum (scouring rush) Ostracoda (aquatic crustaceans) Cypridopsis cf. vidua Limnocythere cf. staplini Limnocythere sp. Candona cf. renoensis Candona sp. A Candona sp. B ?Candonlella sp. ?Heterocypris sp. ?Cycloypris sp. Potamocypris sp. Cyprideis sp. Darwinula sp. Snails and a Clam Pisidium casertanum (clam) Fossaria dalli (aquatic snail) Lymnaea caperata (aquatic snail) Lymnaea cf. elodes (aquatic snail) Bakerilymnaea bulimoides (aquatic snail) Gyraulus parvus (aquatic snail) Promenetus exacuous (aquatic snail) Promenetus umbilicatellus (aquatic snail) Physa virgata (aquatic snail) Gastrocopta cristata (terrestrial snail) Gastrocopta tappaniana (terrestrial snail) Pupoides albilabris (terrestrial snail) Vertigo milium (terrestrial snail) Vertigo ovata (terrestrial snail) cf. Succinea (terrestrial snail) Deroceras aenigma (slug) Hawaila minuscula (terrestrial snail) Fish and Amphibians indeterminate small fish Ambystoma tigrinum (tiger salamander) Scaphiopus hammondi (spadefoot toad) Bufo alvarius (toad) Hyla eximia (tree frog) Rana sp. (leopard frog) Turtles and Lizards Kinosternon arizonense (mud turtle) Terrapene cf. ornata (box turtle) Gopherus sp. (tortoise) Hesperotestudo sp. (giant tortoise) Eumeces sp. (skink) “Cnemidophorus” sp. (whiptail lizard) Crotaphytus sp. (collared lizard) Phrynosoma sp. (horned lizard) Sceloporus sp. -
Hastings Slide Collection3
HASTINGS NATURAL HISTORY RESERVATION SLIDE COLLECTION 1 ORDER FAMILY GENUS SPECIES SUBSPECIES AUTHOR DATE # SLIDES COMMENTS/CORRECTIONS Siphonaptera Ceratophyllidae Diamanus montanus Baker 1895 221 currently Oropsylla (Diamanus) montana Siphonaptera Ceratophyllidae Diamanus spp. 1 currently Oropsylla (Diamanus) spp. Siphonaptera Ceratophyllidae Foxella ignota acuta Stewart 1940 402 syn. of F. ignota franciscana (Roths.) Siphonaptera Ceratophyllidae Foxella ignota (Baker) 1895 2 Siphonaptera Ceratophyllidae Foxella spp. 15 Siphonaptera Ceratophyllidae Malaraeus spp. 1 Siphonaptera Ceratophyllidae Malaraeus telchinum Rothschild 1905 491 M. telchinus Siphonaptera Ceratophyllidae Monopsyllus fornacis Jordan 1937 57 currently Eumolpianus fornacis Siphonaptera Ceratophyllidae Monopsyllus wagneri (Baker) 1904 131 currently Aetheca wagneri Siphonaptera Ceratophyllidae Monopsyllus wagneri ophidius Jordan 1929 2 syn. of Aetheca wagneri Siphonaptera Ceratophyllidae Opisodasys nesiotus Augustson 1941 2 Siphonaptera Ceratophyllidae Orchopeas sexdentatus (Baker) 1904 134 Siphonaptera Ceratophyllidae Orchopeas sexdentatus nevadensis (Jordan) 1929 15 syn. of Orchopeas agilis (Baker) Siphonaptera Ceratophyllidae Orchopeas spp. 8 Siphonaptera Ceratophyllidae Orchopeas latens (Jordan) 1925 2 Siphonaptera Ceratophyllidae Orchopeas leucopus (Baker) 1904 2 Siphonaptera Ctenophthalmidae Anomiopsyllus falsicalifornicus C. Fox 1919 3 Siphonaptera Ctenophthalmidae Anomiopsyllus congruens Stewart 1940 96 incl. 38 Paratypes; syn. of A. falsicalifornicus Siphonaptera -
Reconstruction of Mid Wisconsin Environments in Southern New Mexico
Articles Arthur H. Harris Reconstruction of Mid Wisconsin Environments in Southern New Mexico Abundant vertebrate remains from two mid-Wisconsin cave deposits in New Mexico allow reconstruction of paleoenvironments. Dry Cave lies in southeastern New Mexico, U-Bar Cave in the extreme southwest (Figure 1). Both sites are in the ecotone between woodland and Chihuahuan Desert vegetations. During the mid Wisconsin, both had vertebrate species indicative of woodland, but otherwise differed greatly. Dry Cave had winter temperatures milder than those at the site today, but otherwise the climate was similar to that now found some 450 km to the north. Except for taxa allowed into the area by mild winters, extralimital forms occur in nearby highland woodlands or in northeastern New Mexico. U-Bar Cave probably lacked winter freezes, had cool summers, and had precipitation more evenly distributed than now. Taxa now as distant as the Great Basin occurred together with species from the nearer highlands. Relatively warm summers and retention of seasonal patterns of precipitation at Dry Cave in contrast to cool summers and decreased seasonality of precipitation at U-Bar Cave produced more extreme biotic differences between the sites than is the case now. Whether this was due to different contemporaneous climatic regimes or to chronological differences between the faunas is uncertain. The last major subdivision of the Pleistocene Epoch is the Wisconsin Age. Between ice advances in the early Wisconsin, terminating around 60 000 B.P., and a major renewal of glacial activity in the late Wisconsin, commencing around 32 000 to 27 000 B. P., there was a long span of less severe climatic conditions, the mid Wisconsin (see Bradley 1985 for age estimates). -
Pack Rats (Neotoma Spp.): Keystone Ecological Engineers?
Journal of Arid Environments 74 (2010) 1450e1455 Contents lists available at ScienceDirect Journal of Arid Environments journal homepage: www.elsevier.com/locate/jaridenv Pack rats (Neotoma spp.): Keystone ecological engineers? Walter G. Whitford a, Yosef Steinberger b,* a USDA-ARS Jornada Experimental Range, MSC 3JER, New Mexico State University, Las Cruces, NM 88003, USA b The Mina & Everard Goodman, The Mina & Everard Goodman Faculty of Life Sciences, Bar-Ilan University, Ramat-Gan 52900, Israel article info abstract Article history: The potential role of two species of pack rats (Neotoma albigula and Neotoma micropus) as keystone Received 8 December 2009 ecological engineers was examined by estimating the species diversity of invertebrates living in the nest Received in revised form middens, and nitrogen mineralization rates in soils associated with the middens. Although pack-rat 15 April 2010 middens in tarbush (Flourensia cernua) shrublands were smaller than those in creostebush (Larrea tri- Accepted 21 May 2010 dentata) shrublands, they housed a higher abundance and diversity of arthropods. The Neotoma spp. Available online 15 June 2010 middens were an important microhabitat for crickets (Gryllus sp.), wolf spiders (Lycosa spp.), and lycid beetle larvae (Lycidae) in all of the shrub habitats. There were five arthropod taxa that occupied all Keywords: Habitat middens in the creosote-bush shrubland, and 12 arthropod taxa that occupied all middens in the tarbush fi Mineralization shrubland. Soils associated with pack-rat middens had signi cantly higher soil organic-matter content Species diversity than reference soils. Nitrogen mineralization was significantly higher in soils associated with pack-rat Stick nest middens than in reference soils. -
ARTHROPODA Subphylum Hexapoda Protura, Springtails, Diplura, and Insects
NINE Phylum ARTHROPODA SUBPHYLUM HEXAPODA Protura, springtails, Diplura, and insects ROD P. MACFARLANE, PETER A. MADDISON, IAN G. ANDREW, JOCELYN A. BERRY, PETER M. JOHNS, ROBERT J. B. HOARE, MARIE-CLAUDE LARIVIÈRE, PENELOPE GREENSLADE, ROSA C. HENDERSON, COURTenaY N. SMITHERS, RicarDO L. PALMA, JOHN B. WARD, ROBERT L. C. PILGRIM, DaVID R. TOWNS, IAN McLELLAN, DAVID A. J. TEULON, TERRY R. HITCHINGS, VICTOR F. EASTOP, NICHOLAS A. MARTIN, MURRAY J. FLETCHER, MARLON A. W. STUFKENS, PAMELA J. DALE, Daniel BURCKHARDT, THOMAS R. BUCKLEY, STEVEN A. TREWICK defining feature of the Hexapoda, as the name suggests, is six legs. Also, the body comprises a head, thorax, and abdomen. The number A of abdominal segments varies, however; there are only six in the Collembola (springtails), 9–12 in the Protura, and 10 in the Diplura, whereas in all other hexapods there are strictly 11. Insects are now regarded as comprising only those hexapods with 11 abdominal segments. Whereas crustaceans are the dominant group of arthropods in the sea, hexapods prevail on land, in numbers and biomass. Altogether, the Hexapoda constitutes the most diverse group of animals – the estimated number of described species worldwide is just over 900,000, with the beetles (order Coleoptera) comprising more than a third of these. Today, the Hexapoda is considered to contain four classes – the Insecta, and the Protura, Collembola, and Diplura. The latter three classes were formerly allied with the insect orders Archaeognatha (jumping bristletails) and Thysanura (silverfish) as the insect subclass Apterygota (‘wingless’). The Apterygota is now regarded as an artificial assemblage (Bitsch & Bitsch 2000). -
Fleas (Siphonaptera) Are Cretaceous, and Evolved with Theria
bioRxiv preprint doi: https://doi.org/10.1101/014308; this version posted January 24, 2015. The copyright holder for this preprint (which was not certified by peer review) is the author/funder, who has granted bioRxiv a license to display the preprint in perpetuity. It is made available under aCC-BY-NC-ND 4.0 International license. Fleas (Siphonaptera) are Cretaceous, and Evolved with Theria Qiyun Zhu1, Michael Hastriter2, Michael Whiting2, 3, Katharina Dittmar1, 4* Jan. 23, 2015 Abstract: Fleas (order Siphonaptera) are highly-specialized, diverse blood-feeding ectoparasites of mammals and birds with an enigmatic evolutionary history and obscure origin. We here present a molecular phylogenetic study based on a compre- hensive taxon sampling of 259 flea taxa, representing 16 of the 18 extant families of this order. A Bayesian phylogenetic tree with strong nodal support was recovered, consisting of seven sequentially derived lineages with Macropsyllidae at the base and Stephanocircidae as the second basal group. Divergence times of flea lineages were estimated based on fossil records and host specific associations to bats (Chiroptera), showing that the common ancestor of extant Siphonaptera split from its clos- est mecopteran sister group in the Early Cretaceous and basal lineages diversified during the Late Cretaceous. However, most of the intraordinal divergence into families took place after the K-Pg boundary. Ancestral states of host association and bioge- ographical distribution were reconstructed, suggesting with high likelihood that fleas originated in the southern continents (Gondwana) and migrated from South America to their extant distributions in a relatively short time frame. Theria (placental mammals and marsupials) represent the most likely ancestral host group of extant Siphonaptera, with marsupials occupying a more important role than previously assumed. -
Kenai National Wildlife Refuge Species List, Version 2018-07-24
Kenai National Wildlife Refuge Species List, version 2018-07-24 Kenai National Wildlife Refuge biology staff July 24, 2018 2 Cover image: map of 16,213 georeferenced occurrence records included in the checklist. Contents Contents 3 Introduction 5 Purpose............................................................ 5 About the list......................................................... 5 Acknowledgments....................................................... 5 Native species 7 Vertebrates .......................................................... 7 Invertebrates ......................................................... 55 Vascular Plants........................................................ 91 Bryophytes ..........................................................164 Other Plants .........................................................171 Chromista...........................................................171 Fungi .............................................................173 Protozoans ..........................................................186 Non-native species 187 Vertebrates ..........................................................187 Invertebrates .........................................................187 Vascular Plants........................................................190 Extirpated species 207 Vertebrates ..........................................................207 Vascular Plants........................................................207 Change log 211 References 213 Index 215 3 Introduction Purpose to avoid implying -
Effects of Pleistocene Environmental Changes on the Distribution and Community Structure of the Mammalian Fauna of Mexico
See discussions, stats, and author profiles for this publication at: https://www.researchgate.net/publication/220048614 Effects of Pleistocene environmental changes on the distribution and community structure of the mammalian fauna of Mexico Article in Quaternary Research · May 2010 DOI: 10.1016/j.yqres.2010.02.006 CITATIONS READS 51 350 3 authors: Gerardo Ceballos Joaquin Arroyo-Cabrales Universidad Nacional Autónoma de México Instituto Nacional de Antropología e Historia 285 PUBLICATIONS 9,624 CITATIONS 252 PUBLICATIONS 1,903 CITATIONS SEE PROFILE SEE PROFILE Eduardo Ponce Universidad Nacional Autónoma de México 15 PUBLICATIONS 146 CITATIONS SEE PROFILE Some of the authors of this publication are also working on these related projects: Peces del Estado de México View project Placement of Myotis planiceps within the Myotis phylogeny View project All content following this page was uploaded by Gerardo Ceballos on 01 May 2019. The user has requested enhancement of the downloaded file. Quaternary Research 73 (2010) 464–473 Contents lists available at ScienceDirect Quaternary Research journal homepage: www.elsevier.com/locate/yqres Effects of Pleistocene environmental changes on the distribution and community structure of the mammalian fauna of Mexico Gerardo Ceballos a, Joaquín Arroyo-Cabrales b,⁎, Eduardo Ponce a a Instituto de Ecología, UNAM, Apdo. Postal 70-275; México D.F. 04510, Mexico b Subdirección de Laboratorios y Apoyo Académico, INAH, Moneda # 16, Col. Centro, 06060 México, D.F, Mexico article info abstract Article history: Biological communities in Mexico experienced profound changes in species composition and structure as a Received 22 June 2008 consequence of the environmental fluctuations during the Pleistocene. Based on the recent and fossil Available online 7 April 2010 Mexican mammal checklists, we determine the distribution, composition, diversity, and community structure of late Pleistocene mammalian faunas, and analyze extinction patterns and response of individual Keywords: species to environmental changes. -
Biodiversity from Caves and Other Subterranean Habitats of Georgia, USA
Kirk S. Zigler, Matthew L. Niemiller, Charles D.R. Stephen, Breanne N. Ayala, Marc A. Milne, Nicholas S. Gladstone, Annette S. Engel, John B. Jensen, Carlos D. Camp, James C. Ozier, and Alan Cressler. Biodiversity from caves and other subterranean habitats of Georgia, USA. Journal of Cave and Karst Studies, v. 82, no. 2, p. 125-167. DOI:10.4311/2019LSC0125 BIODIVERSITY FROM CAVES AND OTHER SUBTERRANEAN HABITATS OF GEORGIA, USA Kirk S. Zigler1C, Matthew L. Niemiller2, Charles D.R. Stephen3, Breanne N. Ayala1, Marc A. Milne4, Nicholas S. Gladstone5, Annette S. Engel6, John B. Jensen7, Carlos D. Camp8, James C. Ozier9, and Alan Cressler10 Abstract We provide an annotated checklist of species recorded from caves and other subterranean habitats in the state of Georgia, USA. We report 281 species (228 invertebrates and 53 vertebrates), including 51 troglobionts (cave-obligate species), from more than 150 sites (caves, springs, and wells). Endemism is high; of the troglobionts, 17 (33 % of those known from the state) are endemic to Georgia and seven (14 %) are known from a single cave. We identified three biogeographic clusters of troglobionts. Two clusters are located in the northwestern part of the state, west of Lookout Mountain in Lookout Valley and east of Lookout Mountain in the Valley and Ridge. In addition, there is a group of tro- globionts found only in the southwestern corner of the state and associated with the Upper Floridan Aquifer. At least two dozen potentially undescribed species have been collected from caves; clarifying the taxonomic status of these organisms would improve our understanding of cave biodiversity in the state.