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498 results for “Columbia”
SELFE sediment model benchmark in the Columbia River estuary.
<p>SELFE sediment model benchmark in the Columbia River estuary.</p> <p>This is an archive of the set of SELFE simulations used to benchmark a sediment module against idealized test cases and a realistic scenario in the Columbia River estuary.<br /> Each test is contained in a directory and includes model input files, the binary used, and scripts used for post-processing.<br /> The simulations, data, and analysis were used for the manuscript "Benchmarking an unstructured-grid sediment model in an energetic estuary" by JE Lopez and AM Baptista.</p> <p>The archive consists of data collected from CMOP research cruises and we would like to acknowledge the contributions of Jim Carlson, John Dunlap, Avery Snyder, Keaton Snyder, and Nate Lauffenburger (University of Washington) and Daryl Swensen and Byron Crump (Oregon State University) in the collection of this data.</p>
FIGURE 7 in New Cimbrophlebiidae (Insecta: Mecoptera) from the Early Eocene at McAbee, British Columbia, Canada and Republic, Washington, USA
FIGURE 7. Cimbrophlebia sp. A, UCCIPR L-18 F-998. A, photograph (part); B, drawing (part, no additional information on counterpart); C, reconstruction of the hypothesized complete size and shape of C. sp. A wing (top) based on that of C. flabelliformis (bottom). A, B to scale = 1 cm; C to scale = 1 cm.
FIGURE 6. Cimbrophlebia westae, holotype wing SRUI 099600. A in New Cimbrophlebiidae (Insecta: Mecoptera) from the Early Eocene at McAbee, British Columbia, Canada and Republic, Washington, USA
FIGURE 6. Cimbrophlebia westae, holotype wing SRUI 099600. A, photograph; B, drawing; C, colouration (simplified to two shades) of C. westae wing, note basal portion obscured by staining, rendered blank. A, B to scale = 1 cm; C scale = 1 cm.
FIGURE 4. A, B in New Cimbrophlebiidae (Insecta: Mecoptera) from the Early Eocene at McAbee, British Columbia, Canada and Republic, Washington, USA
FIGURE 4. A, B, Cimbrophlebia brooksi, holotype wing SR062005: A, photograph (part); B, drawing from part and counterpart. C, D, C. brooksi, paratype wing SR990405: C, photograph (part); D, drawing from part and counterpart. A– D to scale = 1 cm.
FIGURE 5 in New Cimbrophlebiidae (Insecta: Mecoptera) from the Early Eocene at McAbee, British Columbia, Canada and Republic, Washington, USA
FIGURE 5. Close-up of mid-anterior portion of C. brooksi paratype wing showing rugose membrane. Scale = 2 mm.
FIGURE 2. Cimbrophlebia leahyi, holotype. A in New Cimbrophlebiidae (Insecta: Mecoptera) from the Early Eocene at McAbee, British Columbia, Canada and Republic, Washington, USA
FIGURE 2. Cimbrophlebia leahyi, holotype. A, photograph of the counterpart TRUIPR L-018 F-1161; B, photograph of the part TRUIPR L-018 F-1160; C, drawing from both the part and counterpart. A–C to scale = 1 cm.
FIGURE 3. Cimbrophlebia leahyi, holotype. A in New Cimbrophlebiidae (Insecta: Mecoptera) from the Early Eocene at McAbee, British Columbia, Canada and Republic, Washington, USA
FIGURE 3. Cimbrophlebia leahyi, holotype. A, drawing of top wing from part and counterpart; B, C, drawings of apical portions of two bottom wings from part and counterpart. A–C to scale = 1 cm.
FIGURE 1. Cimbrophlebia flabelliformis, holotype wing UCCIPR L-18 F-763. A in New Cimbrophlebiidae (Insecta: Mecoptera) from the Early Eocene at McAbee, British Columbia, Canada and Republic, Washington, USA
FIGURE 1. Cimbrophlebia flabelliformis, holotype wing UCCIPR L-18 F-763. A, photograph (part); B, drawing from part and counterpart. A, B to scale = 1 cm.
FIGURE 4 in Zyzzyzus rubusidaeus (Cnidaria, Hydrozoa, Tubulariidae), a new species of anthoathecate hydroid from the coast of British Columbia, Canada
FIGURE 4. Zyzzyzus rubusidaeus, section of hydrocaulus showing longitudinal canals. Scale equals 0.1 mm.
FIGURE 5 in Zyzzyzus rubusidaeus (Cnidaria, Hydrozoa, Tubulariidae), a new species of anthoathecate hydroid from the coast of British Columbia, Canada
FIGURE 5. Cnidocysts of Zyzzyzus rubusidaeus. A, stenotele, small, from oral tentacle. B, stenotele, large, from aboral tentacle. C, microbasic eurytele, from aboral tentacle. D, desmoneme, from oral tentacle. E, desmoneme, from oral tentacle (differential interference contrast). F, isorhiza, large, from hydranth. G, isorhizas, slender, from gonophore. H, basitrich, from gonophore. I, basitrich, discharged, from gonophore.
FIGURE 1 in Zyzzyzus rubusidaeus (Cnidaria, Hydrozoa, Tubulariidae), a new species of anthoathecate hydroid from the coast of British Columbia, Canada
FIGURE 1. Zyzzyzus rubusidaeus, live aggregation of polyps, from nature. A, entire aggregation (collected 30 March 2012). B, closer view of an aggregation, showing polyps and gonophores (collected 28 February 2012). Photo by Neil McDaniel.
FIGURE 3 in Zyzzyzus rubusidaeus (Cnidaria, Hydrozoa, Tubulariidae), a new species of anthoathecate hydroid from the coast of British Columbia, Canada
FIGURE 3. Zyzzyzus rubusidaeus. Diagrams of polyps. a, gonophores on blastosyle, scale 1 mm. b, female gonophores, scale 0.4 mm. c, base of hydrocaulus with two tubers and young polyp, scale 1 mm. d, smaller polyp showing neck (x) and tubers on lower part of hydrocaulus, scale 1 mm.
FIGURE 2 in Zyzzyzus rubusidaeus (Cnidaria, Hydrozoa, Tubulariidae), a new species of anthoathecate hydroid from the coast of British Columbia, Canada
FIGURE 2. Zyzzyzus rubusidaeus, adult and juvenile polyps. Scale for adult equals 0.5 mm; scale for juvenile equals 0.125 mm.
FIGURE 2 in Cottus schitsuumsh, a new species of sculpin (Scorpaeniformes: Cottidae) in the Columbia River basin, Idaho-Montana, USA
FIGURE 2. Outgroup-rooted neighbor-joining tree of Cottus from all available haplotypes based on uncorrected p-distances for cytochrome c subunit 1 sequences. State and province abbreviations are given for North American samples, and river basins are noted for C. beldingii, C. confusus, and C. schitsuumsh in Idaho and Montana. Cottus poecilopus, C. reinii, those in the Cottopsis clade (Kinziger et al. 2005), and the outgroup Leptocottus armatus are not shown.
FIGURE 3 in Cottus schitsuumsh, a new species of sculpin (Scorpaeniformes: Cottidae) in the Columbia River basin, Idaho-Montana, USA
FIGURE 3. Plot of the first two principal coordinates based on 11 microsatellite loci for Cottus schitsuumsh (triangles) and potentially sympatric C. cognatus (diamonds) and C. rhotheus (squares).
FIGURE 1 in Cottus schitsuumsh, a new species of sculpin (Scorpaeniformes: Cottidae) in the Columbia River basin, Idaho-Montana, USA
FIGURE 1. Distribution of specimens of Cottus schitsuumsh (filled circles; type location, unfilled star) examined within the upper Spokane River (the Couer d'Alene and St. Joe rivers) in Idaho and the Clark Fork River in Montana. Locations of specimens of other Cottus species examined from adjacent basins are depicted (unfilled squares); others beyond this area are noted in the text. Inset: Columbia River basin in the United States.
FIGURE 7 in Cottus schitsuumsh, a new species of sculpin (Scorpaeniformes: Cottidae) in the Columbia River basin, Idaho-Montana, USA
FIGURE 7. Lateral pores absent on the caudal peduncle on Cottus schitsuumsh (left) and present on Cottus confusus (right).
Aerial photos and colony counts of nesting colonial waterbirds in the Columbia River Basin, 2023
<p>In many situations, colonial waterbird colony size is best evaluated from aerial photographs taken during the breeding season. This is typically the case where colonies are not accessible or when it is not feasible to count all birds or nests from ground locations or by boat. This dataset presents high resolution aerial imagery and corresponding nest counts of Caspian terns (<em>Hydroprogne caspia</em>), double-crested cormorants (<em>Nannopterum auritum</em>), Brandt's cormorants (<em>Urile penicillatus</em>), California gulls (<em>Larus californicus</em>), ring-billed gulls (<em>Larus delawarensis</em>), and American white pelicans (<em>Pelecanus erythrorhynchos</em>) nesting in the Columbia River Basin, during the 2023 breeding season. Photos were taken from a fixed-wing aircraft during peak nesting, and colony size was estimated by digitizing photos and enumerating visible birds using ArcGIS and DotDotGoose. Colony size was reported as the number of birds on colony, and, in the case of terns and cormorants, the number of active breeding pairs. These data are part of a wider project to evaluate the efficacy of management actions to reduce the impacts of predation by piscivorous colonial waterbirds on Endangered Species Act (ESA)- listed juvenile salmonids (smolts; <em>Oncorhynchus spp.</em>) in the Columbia River Basin.</p>
Subspecies and Distribution. V. v. vulpes Linnaeus, 1758 — N Europe (Scandinavia). V. v. abietorum Merriam, 1900 — SW Canada (Alberta & British Columbia). V. v. aegyptiacus Sonnini, 1816 — Egypt, Israel, and Lybia. V. v. alascensis Merriam, 1900 — Alaska and NW Canada (NW Territories & Yukon). V. v. alpheraky: Satunin, 1906 — Kazakhstan. V. v. anatolica Thomas, 1920 — Turkey. V. v. arabica Thomas, 1902 — Arabian peninsula. V. v. atlantica Wagner, 1841 — Algeria (forested Atlas Mts). V. v. bangsi Merriam, 1900 — NE Canada (Labrador). V. v. barbara Shaw, 1800 — NW Africa (Barbary Coast). V. v. beringiana Middendorff, 1875 — NE Siberia (shore of Bering Strait). V. v. cascadensis Merriam, 1900 — NW USA (Cascade Mountains, Oregon & Washington). V. v. caucasica Dinnik, 1914 — SW Russia (Caucasus). V. v. crucigera Bechstein, 1789 — Europe through N & C Russia. V. v. daurica Ognev, 1931 — E Russia (Amur, Siberia & Transbaikalia). V.v. deletrix Bangs, 1898 — NE Canada (Newfoundland). V. v. dolichocrania Ognev, 1926 — SE Siberia (S Ussuri). V. v. flavescens Gray, 1843 — N Iran. V. v. fulva Desmarest, 1820 — E USA. V. v. griffith: Blyth, 1854 — Afghanistan and N Pakistan. V.v. harrimani Merriam, 1900 — Alaska (Kodiak I). V. v. hoole Swinhoe, 1870 — S China (Fujian to Sichuan). V. v. ichnusae G. S. Miller, 1907 — Corsica and Sardinia. V. v. induta G. S. Miller, 1907 — Cyprus. V. v. jakutensis Ognev, 1923 — E Siberia (S of Yakutsk). V. v. japonica Gray, 1868 — Japan. V. v. karagan Erxleben, 1777 — Mongolia, Kazakhstan, and Kirgizstan. V. v. kenaiensis Merriam, 1900 — Alaska (Kenai Peninsula). V. v. kurdistanica Satunin, 1906 — Armenia and NE Turkey. V. v. macroura Baird, 1852 — USA (Mountain States). V. v. montana Pearson, 1836 — Himalayas form China (Yunnan) to C Pakistan. V. v. mecator Merriam, 1900 — SW USA (California & Nevada). V_ v. ochroxantha Ognev, 1926 — E Russian Turkestan, Aksai, Kirgizstan, Semirechie. V. v. palaestina Thomas, 1920 —Jordan and Lebanon. V.v. peculiosa Kishida, 1924 — Korea. V. v. pusilla Blyth, 1854 — NW India to Irak. V.v. regalis Merriam, 1900 — N Great Plains of Canada and USA. V. v. rubricosa Bangs, 1898 — E Canada. V.v. schrencki Kishida, 1924 — N Japan (Hokkaido) and NE Russia (Sakhalin). V. v. silacea G. S. Miller, 1907 — Iberian Peninsula. V.v. splendidissima Kishida, 1924 — E Russia (N & C Kurile Is). V. v. stepensis Brauner, 1914 — steppes of S Russia. V. v. tobolica Ognev, 1926 — Russia (lower basin of Ob River) V. v. tschiliensis Matschie, 1907 — NE China. Foxes of European origin were introduced into E USA and Canada in the 17" century, subsequently mixed with local subspecies. Also introduced to Australia in 1800s, and the Falkland Islands (Malvinas). in Canidae
Subspecies and Distribution. V. v. vulpes Linnaeus, 1758 — N Europe (Scandinavia). V. v. abietorum Merriam, 1900 — SW Canada (Alberta & British Columbia). V. v. aegyptiacus Sonnini, 1816 — Egypt, Israel, and Lybia. V. v. alascensis Merriam, 1900 — Alaska and NW Canada (NW Territories & Yukon). V. v. alpheraky: Satunin, 1906 — Kazakhstan. V. v. anatolica Thomas, 1920 — Turkey. V. v. arabica Thomas, 1902 — Arabian peninsula. V. v. atlantica Wagner, 1841 — Algeria (forested Atlas Mts). V. v. bangsi Merriam, 1900 — NE Canada (Labrador). V. v. barbara Shaw, 1800 — NW Africa (Barbary Coast). V. v. beringiana Middendorff, 1875 — NE Siberia (shore of Bering Strait). V. v. cascadensis Merriam, 1900 — NW USA (Cascade Mountains, Oregon & Washington). V. v. caucasica Dinnik, 1914 — SW Russia (Caucasus). V. v. crucigera Bechstein, 1789 — Europe through N & C Russia. V. v. daurica Ognev, 1931 — E Russia (Amur, Siberia & Transbaikalia). V.v. deletrix Bangs, 1898 — NE Canada (Newfoundland). V. v. dolichocrania Ognev, 1926 — SE Siberia (S Ussuri). V. v. flavescens Gray, 1843 — N Iran. V. v. fulva Desmarest, 1820 — E USA. V. v. griffith: Blyth, 1854 — Afghanistan and N Pakistan. V.v. harrimani Merriam, 1900 — Alaska (Kodiak I). V. v. hoole Swinhoe, 1870 — S China (Fujian to Sichuan). V. v. ichnusae G. S. Miller, 1907 — Corsica and Sardinia. V. v. induta G. S. Miller, 1907 — Cyprus. V. v. jakutensis Ognev, 1923 — E Siberia (S of Yakutsk). V. v. japonica Gray, 1868 — Japan. V. v. karagan Erxleben, 1777 — Mongolia, Kazakhstan, and Kirgizstan. V. v. kenaiensis Merriam, 1900 — Alaska (Kenai Peninsula). V. v. kurdistanica Satunin, 1906 — Armenia and NE Turkey. V. v. macroura Baird, 1852 — USA (Mountain States). V. v. montana Pearson, 1836 — Himalayas form China (Yunnan) to C Pakistan. V. v. mecator Merriam, 1900 — SW USA (California & Nevada). V_ v. ochroxantha Ognev, 1926 — E Russian Turkestan, Aksai, Kirgizstan, Semirechie. V. v. palaestina Thomas, 1920 —Jordan and Lebanon. V.v. peculiosa Kishida, 1924 — Korea. V. v. pusilla Blyth, 1854 — NW India to Irak. V.v. regalis Merriam, 1900 — N Great Plains of Canada and USA. V. v. rubricosa Bangs, 1898 — E Canada. V.v. schrencki Kishida, 1924 — N Japan (Hokkaido) and NE Russia (Sakhalin). V. v. silacea G. S. Miller, 1907 — Iberian Peninsula. V.v. splendidissima Kishida, 1924 — E Russia (N & C Kurile Is). V. v. stepensis Brauner, 1914 — steppes of S Russia. V. v. tobolica Ognev, 1926 — Russia (lower basin of Ob River) V. v. tschiliensis Matschie, 1907 — NE China. Foxes of European origin were introduced into E USA and Canada in the 17" century, subsequently mixed with local subspecies. Also introduced to Australia in 1800s, and the Falkland Islands (Malvinas).
Subspecies and Distribution. S. g. gracilis Merriam, 1890 — W USA (from E Washington & E Oregon to NE California, and then E to W Montana & E Wyoming to C Colorado, and possibly the Black Hills, South Dakota. Then S to N New Mexico, N Arizona, C Nevada and E & C California). S. g. amphialus Dickey, 1929 — SW USA (occurs only on Santa Rosa I and Santa Cruz I in Santa Barbara County, California). S. g. latifrons Merriam, 1890 — SW Canada (SW British Columbia) S and W to NW USA (Washington and Oregon). The distribution follows the crest of the Cascade Mts. S. g. leucoparia Merriam, 1890 — S USA (found from C Arizona, C New Mexico, and W & C central Texas) S to N Mexico (Coahuila & C Durango). S. g lucasana Merriam, 1890 — NW Mexico (S Baja California N to Santo Domingo on the W coast and La Paz on the E coast). S. g. martirensis Elliot, 1903 — NW Mexico (N & C Baja California). S. g. phenax Merriam, 1890 — SW USA (From California west to crest of Sierra Nevada). in Mephitidae
Subspecies and Distribution. S. g. gracilis Merriam, 1890 — W USA (from E Washington & E Oregon to NE California, and then E to W Montana & E Wyoming to C Colorado, and possibly the Black Hills, South Dakota. Then S to N New Mexico, N Arizona, C Nevada and E & C California). S. g. amphialus Dickey, 1929 — SW USA (occurs only on Santa Rosa I and Santa Cruz I in Santa Barbara County, California). S. g. latifrons Merriam, 1890 — SW Canada (SW British Columbia) S and W to NW USA (Washington and Oregon). The distribution follows the crest of the Cascade Mts. S. g. leucoparia Merriam, 1890 — S USA (found from C Arizona, C New Mexico, and W & C central Texas) S to N Mexico (Coahuila & C Durango). S. g lucasana Merriam, 1890 — NW Mexico (S Baja California N to Santo Domingo on the W coast and La Paz on the E coast). S. g. martirensis Elliot, 1903 — NW Mexico (N & C Baja California). S. g. phenax Merriam, 1890 — SW USA (From California west to crest of Sierra Nevada).
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