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104 results for “California and Nevada”
Subspecies and Distribution. L. c. californicus Gray, 1837 — SW Oregon, and NW California (W USA). L. c. altamirae Nelson, 1904 — SE Tamaulipas (NE Mexico). L. c. asellus Miller, 1899 — SE Coahuila, NE, S Nuevo Leon, E & SE Zacatecas, San Luis Potosi, Aguascalientes, NE tip ofJalisco, N Guanajuato, and NW Querétaro (NC Mexico). L. c. bennettiz Gray, 1843 — SW California (SW USA), and NW Baja California (NW Mexico). L. c. curts Hall, 1951 — Is along the coast of Tamaulipas (NE Mexico). L. c. deserticola Mearns, 1896 — SE Oregon, S Idaho, SW Montana, NE & E California, Nevada, Utah except SE, and NW, W & SW Arizona (W & SW USA), and NW Sonora and NE Baja California (NW Mexico). The population in SW Montanais isolated. L. c. eremicus J. A. Allen, 1894 — S Arizona (SW USA), N Sonora except extreme NW, NW Chihuahua (N Mexico). L. c. festinus Nelson, 1904 — S Querétaro, Hidalgo, and N State of Mexico (C Mexico). L. c. magdalenae Nelson, 1907 — Magdalena I, Baja California Sur (NW Mexico). L. c. martirensis Stowell, 1895 —Baja California except NW & NE and NE Baja California Sur (NW Mexico). L. c. melanotis Mearns, 1890 — S South Dakota, SE Wyoming, Nebraska, E Colorado, Kansas, W Missouri, NE New Mexico, Oklahoma, W Arkansas, and N Texas (C USA). An isolated population exists in E Oklahoma. L. c. merriami Mearns, 1896 — S Texas (S USA), and NE Coahuila, N Tamaulipas, and N Nuevo Leon (NE Mexico). L. c. richardsonii Bachman, 1839 — C California (SW USA). L. c. sheldoni Burt, 1933 — Isla del Carmen, Baja California Sur (NW Mexico). L. c. texianus Waterhouse, 1848 — SE Utah, SW Colorado, NE Arizona, New Mexico except the NE, and W Texas (C USA), Chihuahua except the NW, W, & SW extremes, W Coahuila, E Durango, and NW Zacatecas (NC Mexico). L. c. wallawalla Merriam, 1904 — S Washington, C & W Oregon, NE California, and NW Nevada (NW USA). L. ¢. xanti Thomas, 1898 — Baja California Sur except the NE (NW Mexico). The Black-tailed Jackrabbit has been introduced into Massachusetts, NewJersey, Maryland, Virginia, and S Florida. in Leporidae
Subspecies and Distribution. L. c. californicus Gray, 1837 — SW Oregon, and NW California (W USA). L. c. altamirae Nelson, 1904 — SE Tamaulipas (NE Mexico). L. c. asellus Miller, 1899 — SE Coahuila, NE, S Nuevo Leon, E & SE Zacatecas, San Luis Potosi, Aguascalientes, NE tip ofJalisco, N Guanajuato, and NW Querétaro (NC Mexico). L. c. bennettiz Gray, 1843 — SW California (SW USA), and NW Baja California (NW Mexico). L. c. curts Hall, 1951 — Is along the coast of Tamaulipas (NE Mexico). L. c. deserticola Mearns, 1896 — SE Oregon, S Idaho, SW Montana, NE & E California, Nevada, Utah except SE, and NW, W & SW Arizona (W & SW USA), and NW Sonora and NE Baja California (NW Mexico). The population in SW Montanais isolated. L. c. eremicus J. A. Allen, 1894 — S Arizona (SW USA), N Sonora except extreme NW, NW Chihuahua (N Mexico). L. c. festinus Nelson, 1904 — S Querétaro, Hidalgo, and N State of Mexico (C Mexico). L. c. magdalenae Nelson, 1907 — Magdalena I, Baja California Sur (NW Mexico). L. c. martirensis Stowell, 1895 —Baja California except NW & NE and NE Baja California Sur (NW Mexico). L. c. melanotis Mearns, 1890 — S South Dakota, SE Wyoming, Nebraska, E Colorado, Kansas, W Missouri, NE New Mexico, Oklahoma, W Arkansas, and N Texas (C USA). An isolated population exists in E Oklahoma. L. c. merriami Mearns, 1896 — S Texas (S USA), and NE Coahuila, N Tamaulipas, and N Nuevo Leon (NE Mexico). L. c. richardsonii Bachman, 1839 — C California (SW USA). L. c. sheldoni Burt, 1933 — Isla del Carmen, Baja California Sur (NW Mexico). L. c. texianus Waterhouse, 1848 — SE Utah, SW Colorado, NE Arizona, New Mexico except the NE, and W Texas (C USA), Chihuahua except the NW, W, & SW extremes, W Coahuila, E Durango, and NW Zacatecas (NC Mexico). L. c. wallawalla Merriam, 1904 — S Washington, C & W Oregon, NE California, and NW Nevada (NW USA). L. ¢. xanti Thomas, 1898 — Baja California Sur except the NE (NW Mexico). The Black-tailed Jackrabbit has been introduced into Massachusetts, NewJersey, Maryland, Virginia, and S Florida.
Distribution. Most of the Great Basin and some of the adjacent intermountain areas of W USA,from SE Oregon and NE California through most of C & N Nevada to S Idaho, extreme SW Montana, extreme W Wyoming, and W Utah. An isolated reintroduced population exists in WC Washington. in Leporidae
Distribution. Most of the Great Basin and some of the adjacent intermountain areas of W USA,from SE Oregon and NE California through most of C & N Nevada to S Idaho, extreme SW Montana, extreme W Wyoming, and W Utah. An isolated reintroduced population exists in WC Washington.
Subspecies and Distribution. P.c.erinitusMerriam,1891—fromOregonandSIdahoStoCNevadaandasmallportionofCalifornia,USA. P.c.auripectusJ.A.Allen,1893—fromEUtahandWColoradoStoNEArizonaandNWNewMexico,USA. P.c.delgadilliBenson,1940—knownonlyfromthetypelocalityandsurroundingareasinNWSonora,Mexico. P.c.disparilisGoldman,1932—extremeSWArizona,USA,andasmallportionofNWSonora,Mexico. P.c.douttiGoin,1944—fromextremeSWWyomingSWtoSCUtah,USA. P.c.pallidissimusHuey,1931—knownonlyfromthetypelocalityonSanLuisGonzagaI,BajaCalifornia,Mexico. P.c.pergracilisGoldman,1939—NE&CENevadaandNW&CWUtah,USA. P. c. stephensi Mearns, 1897 — S Nevada, SW Utah, E & SE California, and W Arizona, USA, and NE Baja California, Mexico. in Cricetidae
Subspecies and Distribution. P.c.erinitusMerriam,1891—fromOregonandSIdahoStoCNevadaandasmallportionofCalifornia,USA. P.c.auripectusJ.A.Allen,1893—fromEUtahandWColoradoStoNEArizonaandNWNewMexico,USA. P.c.delgadilliBenson,1940—knownonlyfromthetypelocalityandsurroundingareasinNWSonora,Mexico. P.c.disparilisGoldman,1932—extremeSWArizona,USA,andasmallportionofNWSonora,Mexico. P.c.douttiGoin,1944—fromextremeSWWyomingSWtoSCUtah,USA. P.c.pallidissimusHuey,1931—knownonlyfromthetypelocalityonSanLuisGonzagaI,BajaCalifornia,Mexico. P.c.pergracilisGoldman,1939—NE&CENevadaandNW&CWUtah,USA. P. c. stephensi Mearns, 1897 — S Nevada, SW Utah, E & SE California, and W Arizona, USA, and NE Baja California, Mexico.
Subspecies and Distribution. N.a.albigulaHartley,1894—fromextremeSENevada,Arizona,andmostofNewMexico(SWUSA)SintoNESonoraandCChihuahuastates(NMexico). N.a.brevicaudaDurrant,1934—restrictedtosmallisolatedareaalongtheUtah—Coloradoborder(WUSA). N.a.laplataensisF.W.Miller,1933—SEUtah,SWColorado,NArizona,andNWNewMexico(SWUSA). N.a.mearnsiGoldman,1915—smallregioninextremeSWArizona(SWUSA). N.a.seriTownsend,1912—restrictedtoTiburonIintheSeaofCortez(NWMexico). N.a.sheldoniGoldman,1915—smallregioninextremeNESonoraState(NWMexico). N. a. venusta True, 1894 — SE Californa, extreme S Nevada, and W Arizona (SW USA) and extreme NE Baja California and NW Sonora states (NW Mexico). in Cricetidae
Subspecies and Distribution. N.a.albigulaHartley,1894—fromextremeSENevada,Arizona,andmostofNewMexico(SWUSA)SintoNESonoraandCChihuahuastates(NMexico). N.a.brevicaudaDurrant,1934—restrictedtosmallisolatedareaalongtheUtah—Coloradoborder(WUSA). N.a.laplataensisF.W.Miller,1933—SEUtah,SWColorado,NArizona,andNWNewMexico(SWUSA). N.a.mearnsiGoldman,1915—smallregioninextremeSWArizona(SWUSA). N.a.seriTownsend,1912—restrictedtoTiburonIintheSeaofCortez(NWMexico). N.a.sheldoniGoldman,1915—smallregioninextremeNESonoraState(NWMexico). N. a. venusta True, 1894 — SE Californa, extreme S Nevada, and W Arizona (SW USA) and extreme NE Baja California and NW Sonora states (NW Mexico).
Distribution. Great Basin in EC California and SW Nevada as well as an isolated record from WC Utah (SW USA). in Soricidae
Distribution. Great Basin in EC California and SW Nevada as well as an isolated record from WC Utah (SW USA).
Distribution. Known from scattered records in the Columbia Plateau and N Great Plains of SC British Columbia (SE Canada), N & SE Washington, Oregon, WC Idaho, Montana, NE California, N Nevada, W Wyoming, and N Utah, although these populations are probably connected and additional collecting efforts are needed. in Soricidae
Distribution. Known from scattered records in the Columbia Plateau and N Great Plains of SC British Columbia (SE Canada), N & SE Washington, Oregon, WC Idaho, Montana, NE California, N Nevada, W Wyoming, and N Utah, although these populations are probably connected and additional collecting efforts are needed.
Distribution. Extreme SW Canada (extreme S British Columbia) and W USA (E Washington, E Oregon, California, Idaho, Montana, Wyoming, SW North Dakota, W South Dakota, W Nebraska, Nevada, Colorado, Utah, Arizona, and New Mexico). in Soricidae
Distribution. Extreme SW Canada (extreme S British Columbia) and W USA (E Washington, E Oregon, California, Idaho, Montana, Wyoming, SW North Dakota, W South Dakota, W Nebraska, Nevada, Colorado, Utah, Arizona, and New Mexico).
FIGURES 67–71 in New Freshwater Gomphonemoid Diatoms from Streams in the Sierra Nevada Mountains, California, USA
FIGURES 67–71. Gomphoneis oreophila Stancheva & Kociolek, sp. nov. type material from Rice Creek, California, USA (site 518RCNAPC). SEM images. Internal valve view of the same specimen. Fig. 67 shows a large axial plate and narrow marginal lamina. Fig. 68 central nodule bears a slit-like stigma and recurved proximal raphe ends. Fig 69 detail of the marginal lamina near the central area. Figs 70 and 71 detail of the marginal lamina at the foot pole. Scale bars: Fig. 67 = 10 μm; Fig. 68 = 3 μm; Fig. 70 = 2 μm; Figs 69, 71 = 0.5 μm.
FIGURES 59–66 in New Freshwater Gomphonemoid Diatoms from Streams in the Sierra Nevada Mountains, California, USA
FIGURES 59–66. Gomphoneis oreophila Stancheva & Kociolek, sp. nov. type material from Rice Creek, California, USA (site 518RCNAPC). SEM images. Fig. 59 external valve view. Fig. 60 external valve view of initial cell. Fig. 61 external girdle view. Figs 62 and 63 detail of the head pole. Fig. 64 detail of foot pole with apical pore field. Fig. 65 central area with single circular stigma. Fig. 66 central area of initial cell with single stigma and several sigmoid areolae. Figs showing the same specimen are: 59, 62, 64, and 65; 60, 63, and 66. Scale bars: Figs 59–61 = 10 μm; Fig. 63 = 3 μm; Figs 62, 64, 65, 66 = 2 μm.
FIGURES 46–58 in New Freshwater Gomphonemoid Diatoms from Streams in the Sierra Nevada Mountains, California, USA
FIGURES 46–58. Gomphoneis oreophila Stancheva & Kociolek, sp. nov. type material from Rice Creek, California, USA (site 518RCNAPC). LM images. Figs 46–52, 55–57 valve view. Figs 53, 54 valve view of initial valves. Fig. 58 girdle view. Scale bar: 10 μm.
FIGURES 28–39 in New Freshwater Gomphonemoid Diatoms from Streams in the Sierra Nevada Mountains, California, USA
FIGURES 28–39. Gomphonema sierrianum Stancheva & Kociolek, sp. nov. type material from San Antonio Creek, California, USA (site 533SPILSA). LM images. Figs 28–33, 35–39 valve view. Fig. 34 girdle view. Scale bar: 10 μm.
FIGURES 22–27 in New Freshwater Gomphonemoid Diatoms from Streams in the Sierra Nevada Mountains, California, USA
FIGURES 22–27. Gomphonema californicum Stancheva & Kociolek, sp. nov. type material from Digger Creek, California, USA (site 507DCABSF). SEM images. Figs 22 and 23 show external valve view of the central area with isolated stigma and small depressions (white arrows), surrounded by short striae composed of areolae with variable shape. Figs 24–27 internal valve view. Figs 25 and 26 illustrate the interval view of the central nodule, bearing a slit-like stigma opening and dilated and recurved proximal raphe ends. Figs showing the same specimen are: 24 and 25; 26 and 27. Scale bars: Figs 24, 27 = 10 μm; Figs 22, 23, 25, 26 = 2 μm.
FIGURES 15–21 in New Freshwater Gomphonemoid Diatoms from Streams in the Sierra Nevada Mountains, California, USA
FIGURES 15–21. Gomphonema californicum Stancheva & Kociolek, sp. nov. type material from Digger Creek, California, USA (site 507DCABSF). SEM images. Figs 15, 16, 19, 20 external valve view. Figs 17, 18, 21 external girdle view. Figs 17, 18, 19, 21 show an apical spine at the head pole (white arrows). Fig. 20 illustrates narrow, unornamented area within the apical pore field at the foot pole (white arrowheads). Figs showing the same specimen are: 15 and 19; 16 and 20; 18 and 21. Scale bars: Figs 15–18 = 10 μm; Figs 19–21 = 2 μm.
FIGURES 40–45 in New Freshwater Gomphonemoid Diatoms from Streams in the Sierra Nevada Mountains, California, USA
FIGURES 40–45. Gomphonema sierrianum Stancheva & Kociolek, sp. nov. type material from San Antonio Creek, California, USA (site 533SPILSA). SEM images. Figs 40, 44 internal valve
FIGURES 1–14 in New Freshwater Gomphonemoid Diatoms from Streams in the Sierra Nevada Mountains, California, USA
FIGURES 1–14. Gomphonema californicum Stancheva & Kociolek, sp. nov., LM images. Figs 1, 4, 5, 6 (type material, site 507DCABSF). Figs 3, 10, 12, 13, 14 (site 518RCNAPC). Figs 2, 7, 8, 9, 11 (site 521BTC303). Figs 1–11 valve view. Figs 12 and 13 girdle view; note that the focus on Fig. 13 is on the apical spines. Fig. 14 initial valve. Scale bar: 10 μm.
Insect diversity over 36 years at a protected Sierra Nevada (California) site
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Drainage basins serve as multiple glacial refugia for alpine habitats in the Sierra Nevada Mountains, California
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Data from: From lidar waveforms to vegetation products: 7380 km2 of high-resolution airborne and simulated GEDI data over Sierra Nevada, California
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Climate drivers of summer warming in Emerald Lake, Sierra Nevada, California
Mountain lakes experience extreme inter-annual climate variation as well as rapidly warming air temperatures, making them ideal systems to understand lake-climate responses. Snowpack and water temperature are highly correlated in mountain lakes, but we lack a complete understanding of underlying mechanisms. Motivated by predicted declines in snowfall with future temperature increases, we investigated how surface heat fluxes and lake temperature responded to variation in snowpack, ice-duration, and weather in a typical high elevation lake in the Sierra Nevada, California. Ice duration determined the phenology of lake exposure to solar radiation, and was the dominant mechanism linking snowpack to lake temperature. The relative importance of heat loss fluxes (longwave radiation, latent and sensible heat exchange) varied among wet and dry years. Declines in snowpack and ice cover in mountain systems will reduce the scale of variation in lake thermal responses and increase the responsiveness of lake warming to atmospheric forcing.
FIGURE 7 in A new species of Okanagana from the Walker Lane region of Nevada and California (Hemiptera: Auchenorrhyncha: Cicadidae)
FIGURE 7. Phylogenetic hypothesis for Okanagana boweni sp. n. and relatives.
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