The Extending of Cotton Rat Range in California - Their Life History and Control
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California's Freshwater Fishes: Status and Management
California’s freshwater fishes: status and management Rebecca M. Quiñones* and Peter B. Moyle Center for Watershed Sciences, University of California at Davis, One Shields Ave, Davis, 95616, USA * correspondence to [email protected] SUMMARY Fishes in Mediterranean climates are adapted to thrive in streams with dy- namic environmental conditions such as strong seasonality in flows. Howev- er, anthropogenic threats to species viability, in combination with climate change, can alter habitats beyond native species’ environmental tolerances and may result in extirpation. Although the effects of a Mediterranean cli- mate on aquatic habitats in California have resulted in a diverse fish fauna, freshwater fishes are significantly threatened by alien species invasions, the presence of dams, and water withdrawals associated with agricultural and urban use. A long history of habitat degradation and dependence of salmonid taxa on hatchery supplementation are also contributing to the decline of fish- es in the state. These threats are exacerbated by climate change, which is also reducing suitable habitats through increases in temperatures and chang- es to flow regimes. Approximately 80% of freshwater fishes are now facing extinction in the next 100 years, unless current trends are reversed by active conservation. Here, we review threats to California freshwater fishes and update a five-tiered approach to preserve aquatic biodiversity in California, with emphasis on fish species diversity. Central to the approach are man- agement actions that address conservation at different scales, from single taxon and species assemblages to Aquatic Diversity Management Areas, wa- tersheds, and bioregions. Keywords: alien fishes, climate change, conservation strategy, dams Citation: Quiñones RM, Moyle PB (2015) California’s freshwater fishes: status and man- agement. -
CATALINA CALIFORNIA QUAIL (Callipepla Californica Catalinensis) Paul W
II SPECIES ACCOUNTS Andy Birch PDF of Catalina California Quail account from: Shuford, W. D., and Gardali, T., editors. 2008. California Bird Species of Special Concern: A ranked assessment of species, subspecies, and distinct populations of birds of immediate conservation concern in California. Studies of Western Birds 1. Western Field Ornithologists, Camarillo, California, and California Department of Fish and Game, Sacramento. California Bird Species of Special Concern CATALINA CALIFORNIA QUAIL (Callipepla californica catalinensis) Paul W. Collins Criteria Scores Population Trend 0 Santa Range Trend 0 Barbara County Population Size 7.5 Range Size 10 Ventura Endemism 10 County Population Concentration 10 Threats 0 Los San Miguel Is. Santa Cruz Is. Angeles County Anacapa Is. Santa Rosa Is. Santa Barbara Is. Santa Catalina Is. San Nicolas Is. San Clemente Is. Current Year-round Range Historic Year-round Range County Boundaries Kilometers 20 10 0 20 Current and historic (ca. 1944) year-round range of the Catalina California Quail. Birds from Santa Catalina Island (perhaps brought by Native Americans) later introduced successfully to Santa Rosa (1935–1940) and Santa Cruz (late 1940s) islands, but unsuccessfully to San Nicolas Island (1962); quail from mainland populations of C. c. californica introduced unsuccessfully to Santa Cruz (prior to 1875) and San Clemente (late 19th century, 1913) islands. Catalina California Quail Studies of Western Birds 1:107–111, 2008 107 Studies of Western Birds No. 1 SPECIAL CONCERN PRIORITY HISTORIC RANGE AND ABUNDANCE Currently considered a Bird Species of Special IN CALIFORNIA Concern (year round), priority 3. This subspecies Grinnell and Miller (1944) described the Catalina was not included on prior special concern lists California Quail as a “common to abundant” (Remsen 1978, CDFG 1992). -
Godbois-222-227.Pdf
222 Author’s name Bobcat Diet on an Area Managed for Northern Bobwhite Ivy A. Godbois, Joseph W. Jones Ecological Research Center, Newton, GA 39870 L. Mike Conner, Joseph W. Jones Ecological Research Center, Newton, GA 39870 Robert J. Warren, Warnell School of Forest Resources, University of Georgia, Athens, GA 30602 Abstract: We quantified bobcat (Lynx rufus) diet on a longleaf pine (Pinus palustris) dominated area managed for northern bobwhite (Colinus virginianus), hereafter quail. We sorted prey items to species when possible, but for analysis we categorized them into 1 of 5 classes: rodent, bird, deer, rabbit, and other species. Bobcat diet did not dif- fer seasonally (X2 = 17.82, P = 0.1213). Most scats (91%) contained rodent, 14% con- tained bird, 9% contained deer (Odocoileus virginianus), 6% contained rabbit (Sylvila- gus sp.), and 12% contained other. Quail remains were detected in only 2 of 135 bobcat scats examined. Because of low occurrence of quail (approximately 1.4%) in bobcat scats we suggest that bobcats are not a serious predator of quail. Key Words: bobcat, diet, Georgia, Lynx rufus Proc. Annu. Conf. Southeast. Assoc. Fish and Wildl. Agencies 57:222–227 Bobcats are opportunistic in their feeding habits, and their diet often reflects prey availability (Latham 1951). In the Southeast, bobcats prey most heavily on small mammals such as rabbits and cotton rats (Davis 1955, Beasom and Moore 1977, Miller and Speake 1978, Maehr and Brady 1986, Baker et al. 2001). In some regions, bobcats also consume deer. Deer consumption is often highest during fall- winter when there is the possibility for hunter-wounded deer to be consumed and during spring-summer when fawns are available as prey (Buttrey 1979, Story et al. -
Riqueza De Espécies E Relevância Para a Conservação
O Brasil é reconhecidamente um dos países de megadiversidade de mamíferos do mundo, abrigando cerca de 12% de todas as espécies desse grupo existentes no nosso planeta, distribuídas em 12 Ordens e 50 Famílias. Dentre as espécies que ocorrem no País, 210 (30% do total) são exclusivas do território brasileiro. Esses números não só indicam a importância do País para a conservação mundial desses animais como também trazem para a mastozoologia brasileira a responsabilidade de produzir e disseminar conhecimento científico de qualidade sobre um grupo carismático, bastante ameaçado pela ação antrópica e importante componente dos ecossistemas naturais. O próprio aumento no número de espécies reconhecidas para o Brasil nos últimos 15 anos já é um indicativo da resposta que vem sendo dada pelos pesquisadores do País a esse desafio de gerar conhecimento científico de qualidade sobre os mamíferos. Na publicação pioneira de Fonseca e colaboradores (Lista Anotada dos Mamíferos do Brasil, 1996), houve a indicação de 524 espécies brasileiras de mamíferos. Na compilação mais recente, de 2012, esse número passou para 701, o que representa um aumento de quase 34% em 16 anos (Paglia et al., Lista Anotada dos Mamíferos do Brasil , 2a ed., 2012). Visando contribuir para essa produção de conhecimento científico de qualidade sobre mamíferos, há alguns anos atrás nós organizamos uma publicação que reunia estudos científicos inéditos sobre vários aspectos da biologia do grupo, intitulada Mamíferos do Brasil: Genética, Sistemática, Ecologia e Conservação. Esse livro, publicado em 2006, contou com a participação de vários mastozoólogos brasileiros de destaque. A nossa intenção, com o mesmo, era contribuir para a produção e divulgação da informação científica para um público mais amplo, incluindo alunos de graduação e não-acadêmicos interessados em mastozoologia, além é claro dos pesquisadores especialistas na área. -
Genus/Species Skull Ht Lt Wt Stage Range Abalosia U.Pliocene S America Abelmoschomys U.Miocene E USA A
Genus/Species Skull Ht Lt Wt Stage Range Abalosia U.Pliocene S America Abelmoschomys U.Miocene E USA A. simpsoni U.Miocene Florida(US) Abra see Ochotona Abrana see Ochotona Abrocoma U.Miocene-Recent Peru A. oblativa 60 cm? U.Holocene Peru Abromys see Perognathus Abrosomys L.Eocene Asia Abrothrix U.Pleistocene-Recent Argentina A. illuteus living Mouse Lujanian-Recent Tucuman(ARG) Abudhabia U.Miocene Asia Acanthion see Hystrix A. brachyura see Hystrix brachyura Acanthomys see Acomys or Tokudaia or Rattus Acarechimys L-M.Miocene Argentina A. minutissimus Miocene Argentina Acaremys U.Oligocene-L.Miocene Argentina A. cf. Murinus Colhuehuapian Chubut(ARG) A. karaikensis Miocene? Argentina A. messor Miocene? Argentina A. minutissimus see Acarechimys minutissimus Argentina A. minutus Miocene? Argentina A. murinus Miocene? Argentina A. sp. L.Miocene Argentina A. tricarinatus Miocene? Argentina Acodon see Akodon A. angustidens see Akodon angustidens Pleistocene Brazil A. clivigenis see Akodon clivigenis Pleistocene Brazil A. internus see Akodon internus Pleistocene Argentina Acomys L.Pliocene-Recent Africa,Europe,W Asia,Crete A. cahirinus living Spiny Mouse U.Pleistocene-Recent Israel A. gaudryi U.Miocene? Greece Aconaemys see Pithanotomys A. fuscus Pliocene-Recent Argentina A. f. fossilis see Aconaemys fuscus Pliocene Argentina Acondemys see Pithanotomys Acritoparamys U.Paleocene-M.Eocene W USA,Asia A. atavus see Paramys atavus A. atwateri Wasatchian W USA A. cf. Francesi Clarkforkian Wyoming(US) A. francesi(francesci) Wasatchian-Bridgerian Wyoming(US) A. wyomingensis Bridgerian Wyoming(US) Acrorhizomys see Clethrionomys Actenomys L.Pliocene-L.Pleistocene Argentina A. maximus Pliocene Argentina Adelomyarion U.Oligocene France A. vireti U.Oligocene France Adelomys U.Eocene France A. -
Section 5 References
Section 5 References 5.0 REFERENCES Akçakaya, H. R. and J. L. Atwood. 1997. A habitat-based metapopulation model of the California Gnatcatcher. Conservation Biology 11:422-434. Akçakaya, H.R. 1998. RAMAS GIS: Linking landscape data with population viability analysis (version 3.0). Applied Biomathematics, Setaauket, New York. Anderson, D.W. and J.W. Hickey. 1970. Eggshell changes in certain North American birds. Ed. K. H. Voous. Proc. (XVth) Inter. Ornith. Congress, pp 514-540. E.J. Brill, Leiden, Netherlands. Anderson, D.W., J.R. Jehl, Jr., R.W. Risebrough, L.A. Woods, Jr., L.R. Deweese, and W.G. Edgecomb. 1975. Brown pelicans: improved reproduction of the southern California coast. Science 190:806-808. Atwood, J.L. 1980. The United States distribution of the California black-tailed gnatcatcher. Western Birds 11: 65-78. Atwood, J.L. 1990. Status review of the California gnatcatcher (Polioptila californica). Unpublished Technical Report, Manomet Bird Observatory, Manomet, Massachusetts. Atwood, J.L. 1992. A maximum estimate of the California gnatcatcher’s population size in the United States. Western Birds. 23:1-9. Atwood, J.L. and J.S. Bolsinger. 1992. Elevational distribution of California gnatcatchers in the United States. Journal of Field Ornithology 63:159-168. Atwood, J.L., S.H. Tsai, C.H. Reynolds, M.R. Fugagli. 1998. Factors affecting estimates of California gnatcatcher territory size. Western Birds 29: 269-279. Baharav, D. 1975. Movement of the horned lizard Phrynosoma solare. Copeia 1975: 649-657. Barry, W.J. 1988. Management of sensitive plants in California state parks. Fremontia 16(2):16-20. Beauchamp, R.M. -
Birds on San Clemente Island, As Part of Our Work Toward the Recovery of the Island’S Endangered Species
WESTERN BIRDS Volume 36, Number 3, 2005 THE BIRDS OF SAN CLEMENTE ISLAND BRIAN L. SULLIVAN, PRBO Conservation Science, 4990 Shoreline Hwy., Stinson Beach, California 94970-9701 (current address: Cornell Laboratory of Ornithology, 159 Sapsucker Woods Rd., Ithaca, New York 14850) ERIC L. KERSHNER, Institute for Wildlife Studies, 2515 Camino del Rio South, Suite 334, San Diego, California 92108 With contributing authors JONATHAN J. DUNN, ROBB S. A. KALER, SUELLEN LYNN, NICOLE M. MUNKWITZ, and JONATHAN H. PLISSNER ABSTRACT: From 1992 to 2004, we observed birds on San Clemente Island, as part of our work toward the recovery of the island’s endangered species. We increased the island’s bird list to 317 species, by recording many additional vagrants and seabirds. The list includes 20 regular extant breeding species, 6 species extirpated as breeders, 5 nonnative introduced species, and 9 sporadic or newly colonizing breeding species. For decades San Clemente Island had been ravaged by overgrazing, especially by goats, which were removed completely in 1993. Since then, the island’s vegetation has begun recovering, and the island’s avifauna will likely change again as a result. We document here the status of that avifauna during this transitional period of re- growth, between the island’s being largely denuded of vegetation and a more natural state. It is still too early to evaluate the effects of the vegetation’s still partial recovery on birds, but the beginnings of recovery may have enabled the recent colonization of small numbers of Grasshopper Sparrows and Lazuli Buntings. Sponsored by the U. S. Navy, efforts to restore the island’s endangered species continue—among birds these are the Loggerhead Shrike and Sage Sparrow. -
Genetic Diversity Between and Within the Arenavirus Species Indigenous to Western Venezuela ☆
View metadata, citation and similar papers at core.ac.uk brought to you by CORE provided by Elsevier - Publisher Connector Virology 378 (2008) 205–213 Contents lists available at ScienceDirect Virology journal homepage: www.elsevier.com/locate/yviro Genetic diversity between and within the arenavirus species indigenous to western Venezuela ☆ Charles F. Fulhorst a,⁎, Maria N.B. Cajimat b, Mary Louise Milazzo a, Hector Paredes c, Nuris M.C. de Manzione c, Rosa A. Salas d,1, Pierre E. Rollin e, Thomas G. Ksiazek e a University of Texas Medical Branch, Department of Pathology, 301 University Boulevard, Galveston, Texas 77555-0609, USA b University of Texas Medical Branch, Graduate School of Biomedical Sciences, Microbiology and Immunology Graduate Program, 301 University Boulevard, Galveston, Texas 77555-1019, USA c Centro de Investigaciones de Virosis Hemorrágicas y Enfermedades Transmisibles, Sector La Colonia Parte Alta, Via Escuela Granja, Quinta CIVIHET, Guanare, Estado Portuguesa, Venezuela d Instituto Nacional de Higiene “Rafael Rangel”, Ciudad Universitaria, Los Chaguaramos, Caracas, Venezuela e Centers for Disease Control and Prevention, Special Pathogens Branch, Atlanta, Georgia 30333, USA article info abstract Article history: The results of analyses of Z, RNA-dependent RNA polymerase, glycoprotein precursor, and nucleocapsid protein Received 4 October 2007 gene sequence data suggested that Guanarito virus was the most common cause of Venezuelan hemorrhagic Returned to author for revision fever in a 7-year period in the 1990s and that the evolution of Pirital virus in association with Sigmodon 27 March 2008 alstoni (Alston's cotton rat) has occurred at a significantly higher rate than the evolution of Guanarito virus in Accepted 13 May 2008 association with Zygodontomys brevicauda (short-tailed cane mouse) on the plains of western Venezuela. -
Life History Account for Hispid Cotton
California Wildlife Habitat Relationships System California Department of Fish and Wildlife California Interagency Wildlife Task Group HISPID COTTON RAT Sigmodon hispidus Family: MURIDAE Order: RODENTIA Class: MAMMALIA M123 Written by: P. Brylski Reviewed by: H. Shellhammer Edited by: R. Duke DISTRIBUTION, ABUNDANCE, AND SEASONALITY In California, occurs only along the Colorado River and in the Imperial Valley. Establishment of cotton rats in the Imperial Valley apparently was in response to agricultural irrigation practices (Dixon 1922). Most common in grassland and cropland habitats near water (Fleharty and Mares 1973, Kaufman and Fleharty 1974), including grass-forb understories in early successional stages of other habitats (McClenaghan and Gaines 1978). Also occurs in overgrown clearings, and herbaceous borders of fields and brushy areas (Hall and Dalquest 1963). SPECIFIC HABITAT REQUIREMENTS Feeding: Feeds mainly on grasses, eating insects seasonally. Food is not stored. Runways are made through dense herbaceous growth, and are similar in appearance to vole runways but much larger. Sometimes feeds on sugar beets, citrus, and other crops. Cover: Tall, dense grass is preferred. Reproduction: Nests of woven grass are constructed either in burrows or on the surface (Baar et al. 1974). Water: No data found, but probably requires free water. Pattern: Grasslands, overgrown clearings and herbaceous borders of fields, and brushy areas are preferred. SPECIES LIFE HISTORY Activity Patterns: Both nocturnal and diurnal, with bimodal nocturnal activity pattern (Kilduff and Dube 1979). Active yearlong. Seasonal Movements/Migration: None. Home Range: Home range averaged 0.35 to 0.39 ha (0.86 to 0.96 ac) for males, and 0.22 ha (0.54 ac) for females (Fleharty and Mares 1973, Layne 1974). -
General Biology of Major Prey Species of the California Spotted Owl
Chapter 10 General Biology of Major Prey Species of the California Spotted Owl Daniel F. Williams, Jared Verner, Howard F. Sakai, and Jeffrey R. Waters Full understanding of the habitat relations of California geographic range (see color photo 5-29). They are most numer- spotted owls depends, in part, on knowledge of the habitat ous where shrub cover is dense, and least abundant in open areas relations of their primary prey species. For example, the north- (Fitch 1947). They are one of few small mammal species of ern flying squirrel is the primary prey of the owl in conifer chaparral habitats that flourish in old, dense stands (Quinn 1990). forests of the Sierra Nevada, comprising as much as 61 to 77 Habitats that are unsuited or poorly suited for dusky-footed percent of the total biomass eaten in some localities and seasons woodrats include open grasslands or fallow, weedy ground; (table 4A). The dusky-footed woodrat is the primary prey in sparsely wooded forests; woodlands solely of conifers or with lower-elevation forests and woodlands of the Sierra Nevada and little shrub understory; and pure stands of chamise, manzanita, throughout all habitats in southern California, making up 74-94 or ceanothus (Linsdale and Tevis 1951). percent of the diet, by weight, in various areas. Current evidence In the Sierra Nevada, this woodrat occurs generally below indicates that suitable nest sites and the most common foods of 5,000 feet in elevation (lower in the north-about 3,300 feet at northern flying squirrels are usually found together in mature Mt. -
Guide to the Coastal Marine Fishes of California
STATE OF CALIFORNIA THE RESOURCES AGENCY DEPARTMENT OF FISH AND GAME FISH BULLETIN 157 GUIDE TO THE COASTAL MARINE FISHES OF CALIFORNIA by DANIEL J. MILLER and ROBERT N. LEA Marine Resources Region 1972 ABSTRACT This is a comprehensive identification guide encompassing all shallow marine fishes within California waters. Geographic range limits, maximum size, depth range, a brief color description, and some meristic counts including, if available: fin ray counts, lateral line pores, lateral line scales, gill rakers, and vertebrae are given. Body proportions and shapes are used in the keys and a state- ment concerning the rarity or commonness in California is given for each species. In all, 554 species are described. Three of these have not been re- corded or confirmed as occurring in California waters but are included since they are apt to appear. The remainder have been recorded as occurring in an area between the Mexican and Oregon borders and offshore to at least 50 miles. Five of California species as yet have not been named or described, and ichthyologists studying these new forms have given information on identification to enable inclusion here. A dichotomous key to 144 families includes an outline figure of a repre- sentative for all but two families. Keys are presented for all larger families, and diagnostic features are pointed out on most of the figures. Illustrations are presented for all but eight species. Of the 554 species, 439 are found primarily in depths less than 400 ft., 48 are meso- or bathypelagic species, and 67 are deepwater bottom dwelling forms rarely taken in less than 400 ft. -
Wildlife in Drought Conditions
SOUTH TEXAS WILDLIFE J. R. THOMASSON A publication of the Caesar Kleberg Wildlife Research Institute Fall 2006 at Texas A&M University-Kingsville Volume 0, No. 3 reduced search and handling times for the bobcat. The former Director of the CKWRI, Dr. Sam Beasom, headed research in the early 970s that stud- ied bobcat diets in southern Texas. He examined 5 bobcat stomachs during a dry year (97), and com- pared the findings to 74 stomachs from a wet year (972). During the dry year, bobcats consumed 2 prey species. Although cotton rats and rabbits were not commonly observed in the wild in 97, they still were the dominant prey accounting for 38% and 8% by volume in bobcat stomachs, respectively. In 972, fol- lowing rainfall that enhanced habitat conditions, over 00 cotton rats per mile were observed several times. Because of the abundance of cotton © Tom Urban rats and rabbits following rainfall, bobcat diet contained these 2 species Bobcats and Drought enough, then cascading effects almost exclusively. This was appar- eventually impact bobcats through ent when comparisons by percent by Michael Tewes and reduction of their prey base as fewer occurrence in the bobcat diet were Lon Grassman, Jr. rodents and rabbits occur. In Texas, the hispid cotton rat This Issue Drought conditions can have and eastern cottontail are important severe consequences on wildlife in bobcat diets. They are large-size South Texas Bobcats page 1 in Texas. We often hear of dismal prey, relative to the other potential By The Numbers page 2 harvest predictions for deer and prey, with rabbits weighing 2–4 quail following extended dry peri- lbs and cotton rats about 9 oz.