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554 results for “Wilson”
On following pages: 26. Common Dwarf Bonneted Bat (Eumops bonariensis); 27. Chimera's Bonneted Bat (Eumops 30. Delta Bonneted Bat (Eumops delticus); 31. Fierce Bonneted Bat (Eumops ferox); 32. Florida Bonneted Bat (Eumops hansae); 35. Guianan Bonneted Bat (Eumops maurus); 36. Northern Dwarf Bonneted Bat (Eumops nanus); 37. Patagonian 39. Trumbull's Bonneted Bat (Eumops trumbull)); 40. Underwood's Bonneted Bat (Eumops underwoodi); 41. Wilson's chimaera); 28. Chiribaya's Bonneted Bat (Eumops chiribaya); 29. Big Bonneted Bat (Eumops dabbenei); floridanus); 33. Wagner's Bonneted Bat (Eumops glaucinus); 34. Sanborn's Bonneted Bat (Eumops Dwarf Bonneted Bat (Eumops patagonicus); 38. Western Bonneted Bat (Eumops perotis), Bonneted Bat (Eumops wilsoni). in Molossidae
On following pages: 26. Common Dwarf Bonneted Bat (Eumops bonariensis); 27. Chimera's Bonneted Bat (Eumops 30. Delta Bonneted Bat (Eumops delticus); 31. Fierce Bonneted Bat (Eumops ferox); 32. Florida Bonneted Bat (Eumops hansae); 35. Guianan Bonneted Bat (Eumops maurus); 36. Northern Dwarf Bonneted Bat (Eumops nanus); 37. Patagonian 39. Trumbull's Bonneted Bat (Eumops trumbull)); 40. Underwood's Bonneted Bat (Eumops underwoodi); 41. Wilson's chimaera); 28. Chiribaya's Bonneted Bat (Eumops chiribaya); 29. Big Bonneted Bat (Eumops dabbenei); floridanus); 33. Wagner's Bonneted Bat (Eumops glaucinus); 34. Sanborn's Bonneted Bat (Eumops Dwarf Bonneted Bat (Eumops patagonicus); 38. Western Bonneted Bat (Eumops perotis), Bonneted Bat (Eumops wilsoni).
Subspecies and Distribution. A.m.minimusE.GeoffroySaint-Hilaire,1803—TasmaniaandtheBassStraitIs. A. m. maritimus Finlayson, 1958 — SE Australia, in S Victoria (W from S Gippsland and Wilson's Promontory and nearby Sunday, Kanowna, and Great Glennie Is) W to SE South Australia (to Robe). in Dasyuridae
Subspecies and Distribution. A.m.minimusE.GeoffroySaint-Hilaire,1803—TasmaniaandtheBassStraitIs. A. m. maritimus Finlayson, 1958 — SE Australia, in S Victoria (W from S Gippsland and Wilson's Promontory and nearby Sunday, Kanowna, and Great Glennie Is) W to SE South Australia (to Robe).
Subspecies and Distribution. S.f.floridanusJ.A.Allen,1890—FloridaPeninsulaexceptSEtip(SEUSA). S.f.alacerBangs,1896—CSUSA,inSEKansas,C&SMissouri,EOklahoma,Arkansas,extremeWTennessee,ETexas,mostofMississippi,extremeWCAlabama,andLouisiana.S.fammophilusHowell,1939—EtipoftheFloridaPeninsula(SEUSA).S.faviusOsgood,1910—ConejoI(LosTestigos),offNEVenezuela.S.faztecus].A.Allen,1890—S&EOaxaca,andSWtipofChiapas(SWMexico). S.f.chapmani].A.Allen,1899—W&STexas(SUSA),ECoahuila,N&ENuevoLeon,andmostofTamaulipas(NEMexico). S.f.chiapensisNelson,1904—NEtipofOaxacaandC&SChiapas(Mexico),andWGuatemala. S.f.connectensNelson,1904—STamaulipas,VeracruzexcepttheS,SanLuisPotosi,NEQuerétaro,NEHidalgo,NPuebla,andNOaxaca(EMexico). S.f.continentisOsgood,1912—NWVenezuela. S.f.costaricensisHarris1933—NWCostaRica. S.f.cumanicusThomas,1897—N&CVenezuela. S.f.hesperiusHoffmeister&Lee,1963—NW&CArizona(SWUSA). S.f.hitchensiMearns,1911—SmithandFishermanIsinNorthamptonCounty,EVirginia(EUSA). S.f.holzneriMearns,1896—SEArizona,andSWtipofNewMexico(SWUSA),ESonora,Chihuahua,WDurango,WZacatecas,andESinaloa(NWMexico). S.f.hondurensisGoldman,1932—SEGuatemala,SW&SHonduras,ElSalvador,andNW&CNicaragua. S.fllanensisBlair,1938—SWKansas,SEtipofColorado,WOklahoma,andNCTexas(CUSA). S.f.macrocorpusDiersing&Wilson,1980—Nayarit,SWJalisco,andSWMichoacan(WMexico). S.f.mallurusThomas,1898—EUSA,fromMaineSWtoE&SPennsylvania,andEWestVirginia,WthroughSKentuckytomostofTennessee(excepttheextremeW),andStomostofAlabama(excepttheextremeW)andNFlorida. S.f.margaritaeMiller,1898—MargaritaI,offNVenezuela. S.f.mearnsii].A.Allen,1894—NC&NEUSA,fromMinnesotaEtoMichigan,andStoENebraska,NEKansas,NMissouri,Kentucky,NWtipofVirginia,WWestVirginia,Ohio,N&WPennsylvania,NW&NNewYork,andWVermont,alsoSC&SECanada,inSEOntario,andSEQuebec. S.f.nigronuchalisHartert,1894—ArubaandCuracaoIs(NetherlandsAntilles),offNVenezuela. S.f.orinociThomas,1900—VichadaDepartment(EColombia)andVenezuelaSoftheOrinocoRiver. S.f.orizabaeMerriam,1893—SECoahuila,SWNuevoLeon,SEZacatecas,SanLuisPotosi,Guanajuato,Querétaro,Hidalgo,NWVeracruz,México,andPuebla(CMexico).S.fpaulsoniSchwartz,1956—SEtipoftheFloridaPeninsula(SEUSA). S.f.purgatusThomas,1920—CundinamarcaandTolimaDepartments(CColombia). S.f.restrictusNelson,1907—SWNayarit,C&SJalisco,EColima,andSWMichoacan(Mexico). S.f.russatusJ.A.Allen,1904—SEtipofVeracruz(Mexico). S.f.similisNelson,1907—NCUSA,fromNorthDakota,SWMontana,andNWMinnesotaStoNE&SEWyoming,NEColorado,andNKansas,alsoinSCCanada,SManitoba,andSESaskatchewan(Canada). S.f.subcinctusMiller,1899—Aguascalientes,C&NEJalisco,SWGuanajuato,andNMichoacan(Mexico). S. f. superciliarisJ. A. Allen, 1899 — La Guajira, Magdalena, Atlantico and Bolivar departments (N Colombia). S. [> yucatanicus Miller, 1899 — NW Yucatan Peninsula (SE Mexico). The subspecies mearnsii has been introduced into Vancouver I (SW Canada) and into Washington and Oregon states (NW USA). Also introduced into Italy and the Alps. in Leporidae
Subspecies and Distribution. S.f.floridanusJ.A.Allen,1890—FloridaPeninsulaexceptSEtip(SEUSA). S.f.alacerBangs,1896—CSUSA,inSEKansas,C&SMissouri,EOklahoma,Arkansas,extremeWTennessee,ETexas,mostofMississippi,extremeWCAlabama,andLouisiana.S.fammophilusHowell,1939—EtipoftheFloridaPeninsula(SEUSA).S.faviusOsgood,1910—ConejoI(LosTestigos),offNEVenezuela.S.faztecus].A.Allen,1890—S&EOaxaca,andSWtipofChiapas(SWMexico). S.f.chapmani].A.Allen,1899—W&STexas(SUSA),ECoahuila,N&ENuevoLeon,andmostofTamaulipas(NEMexico). S.f.chiapensisNelson,1904—NEtipofOaxacaandC&SChiapas(Mexico),andWGuatemala. S.f.connectensNelson,1904—STamaulipas,VeracruzexcepttheS,SanLuisPotosi,NEQuerétaro,NEHidalgo,NPuebla,andNOaxaca(EMexico). S.f.continentisOsgood,1912—NWVenezuela. S.f.costaricensisHarris1933—NWCostaRica. S.f.cumanicusThomas,1897—N&CVenezuela. S.f.hesperiusHoffmeister&Lee,1963—NW&CArizona(SWUSA). S.f.hitchensiMearns,1911—SmithandFishermanIsinNorthamptonCounty,EVirginia(EUSA). S.f.holzneriMearns,1896—SEArizona,andSWtipofNewMexico(SWUSA),ESonora,Chihuahua,WDurango,WZacatecas,andESinaloa(NWMexico). S.f.hondurensisGoldman,1932—SEGuatemala,SW&SHonduras,ElSalvador,andNW&CNicaragua. S.fllanensisBlair,1938—SWKansas,SEtipofColorado,WOklahoma,andNCTexas(CUSA). S.f.macrocorpusDiersing&Wilson,1980—Nayarit,SWJalisco,andSWMichoacan(WMexico). S.f.mallurusThomas,1898—EUSA,fromMaineSWtoE&SPennsylvania,andEWestVirginia,WthroughSKentuckytomostofTennessee(excepttheextremeW),andStomostofAlabama(excepttheextremeW)andNFlorida. S.f.margaritaeMiller,1898—MargaritaI,offNVenezuela. S.f.mearnsii].A.Allen,1894—NC&NEUSA,fromMinnesotaEtoMichigan,andStoENebraska,NEKansas,NMissouri,Kentucky,NWtipofVirginia,WWestVirginia,Ohio,N&WPennsylvania,NW&NNewYork,andWVermont,alsoSC&SECanada,inSEOntario,andSEQuebec. S.f.nigronuchalisHartert,1894—ArubaandCuracaoIs(NetherlandsAntilles),offNVenezuela. S.f.orinociThomas,1900—VichadaDepartment(EColombia)andVenezuelaSoftheOrinocoRiver. S.f.orizabaeMerriam,1893—SECoahuila,SWNuevoLeon,SEZacatecas,SanLuisPotosi,Guanajuato,Querétaro,Hidalgo,NWVeracruz,México,andPuebla(CMexico).S.fpaulsoniSchwartz,1956—SEtipoftheFloridaPeninsula(SEUSA). S.f.purgatusThomas,1920—CundinamarcaandTolimaDepartments(CColombia). S.f.restrictusNelson,1907—SWNayarit,C&SJalisco,EColima,andSWMichoacan(Mexico). S.f.russatusJ.A.Allen,1904—SEtipofVeracruz(Mexico). S.f.similisNelson,1907—NCUSA,fromNorthDakota,SWMontana,andNWMinnesotaStoNE&SEWyoming,NEColorado,andNKansas,alsoinSCCanada,SManitoba,andSESaskatchewan(Canada). S.f.subcinctusMiller,1899—Aguascalientes,C&NEJalisco,SWGuanajuato,andNMichoacan(Mexico). S. f. superciliarisJ. A. Allen, 1899 — La Guajira, Magdalena, Atlantico and Bolivar departments (N Colombia). S. [> yucatanicus Miller, 1899 — NW Yucatan Peninsula (SE Mexico). The subspecies mearnsii has been introduced into Vancouver I (SW Canada) and into Washington and Oregon states (NW USA). Also introduced into Italy and the Alps.
On following pages: 4. Golden Spiny Mouse (Acomys russatus); 5. Arabian Spiny Mouse (Acomys dimidiatus); 6. Seurat's Spiny Mouse (Acomys seurati); 7. Northeast African Spiny Mouse (Acomys cahirinus); 8. Louise's Spiny Mouse (Acomys louisae); 9. Mullah Spiny Mouse (Acomys mullah); 10. Chudeau''s Spiny Mouse (Acomys chudeaui); 11. John's Spiny Mouse (Acomys johannis); 12. Gray Spiny Mouse (Acomys cineraceus); 13. Percival's Spiny Mouse (Acomys percivali); 14. Wilson's Spiny Mouse (Acomys wilsoni); 15. Kemp's Spiny Mouse (Acomys kempi); 16. Fiery Spiny Mouse (Acomys ignitus); 17. Muze Spiny Mouse (Acomys muzel); 18. Nguru Spiny Mouse (Acomys ngurui); 19. Southern African Spiny Mouse (Acomys spinosissimus); 20. Selous's Spiny Mouse (Acomys selousi); 21. Cape Spiny Mouse (Acomys subspinosus); 22. Congo Forest Rat (Deomys ferrugineus). in Muridae
On following pages: 4. Golden Spiny Mouse (Acomys russatus); 5. Arabian Spiny Mouse (Acomys dimidiatus); 6. Seurat's Spiny Mouse (Acomys seurati); 7. Northeast African Spiny Mouse (Acomys cahirinus); 8. Louise's Spiny Mouse (Acomys louisae); 9. Mullah Spiny Mouse (Acomys mullah); 10. Chudeau''s Spiny Mouse (Acomys chudeaui); 11. John's Spiny Mouse (Acomys johannis); 12. Gray Spiny Mouse (Acomys cineraceus); 13. Percival's Spiny Mouse (Acomys percivali); 14. Wilson's Spiny Mouse (Acomys wilsoni); 15. Kemp's Spiny Mouse (Acomys kempi); 16. Fiery Spiny Mouse (Acomys ignitus); 17. Muze Spiny Mouse (Acomys muzel); 18. Nguru Spiny Mouse (Acomys ngurui); 19. Southern African Spiny Mouse (Acomys spinosissimus); 20. Selous's Spiny Mouse (Acomys selousi); 21. Cape Spiny Mouse (Acomys subspinosus); 22. Congo Forest Rat (Deomys ferrugineus).
FIGURE. Photos showing the broader stamens in Tulipa toktogulica compared to T. talassica. A. Tulipa toktogulica. B. Tulipa talassica. Photos by Brett Wilson and Georgy Lazkov in Tulipa toktogulica (Liliaceae), a cryptic, endangered new species from the western Tien-Shan, Kyrgyzstan
FIGURE. Photos showing the broader stamens in Tulipa toktogulica compared to T. talassica. A. Tulipa toktogulica. B. Tulipa talassica. Photos by Brett Wilson and Georgy Lazkov
Supplementary material 1 from: Wilson CE, Castro KL, Thurston GB, Sissons A (2016) Pathway risk analysis of weed seeds in imported grain: A Canadian perspective. In: Daehler CC, van Kleunen M, Pyšek P, Richardson DM (Eds) Proceedings of 13th International EMAPi conference, Waikoloa, Hawaii. NeoBiota 30: 49–74. https://doi.org/10.3897/neobiota.30.7502
Weed seed contaminant species reported in imported grain in a Canadian sampling program 2007–2015 : Explanation note: Complete list of weed seed contaminant species reported in 947 samples of 10 imported grain crops in a Canadian sampling program 2007–2015, cross-listed to number of times reported and crops reported in.
Supplementary material 4 from: Novoa A, Kumschick S, Richardson DM, Rouget M, Wilson JRU (2016) Native range size and growth form in Cactaceae predict invasiveness and impact. In: Daehler CC, van Kleunen M, Pyšek P, Richardson DM (Eds) Proceedings of 13th International EMAPi conference, Waikoloa, Hawaii. NeoBiota 30: 75–90. https://doi.org/10.3897/neobiota.30.7253
Results of the General Impact Scoring System applied to 70 cactus species (35 invasive and 35 non-invasive cactus species with a long history of introduction in South Africa) : Explanation note: The impact scores are expressed as the maximum impact over all the environmental and socioeconomic categories considered in this study.
Supplementary material 3 from: Novoa A, Kumschick S, Richardson DM, Rouget M, Wilson JRU (2016) Native range size and growth form in Cactaceae predict invasiveness and impact. In: Daehler CC, van Kleunen M, Pyšek P, Richardson DM (Eds) Proceedings of 13th International EMAPi conference, Waikoloa, Hawaii. NeoBiota 30: 75–90. https://doi.org/10.3897/neobiota.30.7253
Generic Impact Scoring System (GISS) : Explanation note: Detailed description of impact categories. An updated Excel version is available from the authors on request.
Supplementary material 2 from: Wilson CE, Castro KL, Thurston GB, Sissons A (2016) Pathway risk analysis of weed seeds in imported grain: A Canadian perspective. In: Daehler CC, van Kleunen M, Pyšek P, Richardson DM (Eds) Proceedings of 13th International EMAPi conference, Waikoloa, Hawaii. NeoBiota 30: 49–74. https://doi.org/10.3897/neobiota.30.7502
Frequency distributions showing percentage samples with number of contaminant species reported per sample for 10 imported grain crops examined in a Canadian sampling program 2007–2015 : Explanation note: Ten frequency distribution graphs (one per crop) shown in a multi-panel.
Supplementary material 5 from: Williamson TE, Brusatte SL, Wilson GP (2014) The origin and early evolution of metatherian mammals: the Cretaceous record. ZooKeys 465: 1-76. https://doi.org/10.3897/zookeys.465.8178
Data used to calculate taxonomic richness for Metatherian shown in Figure 15.: Explanation note: Data used to calculate taxonomic richness for Metatheria shown in Figure 15.
Supplementary material 4 from: Williamson TE, Brusatte SL, Wilson GP (2014) The origin and early evolution of metatherian mammals: the Cretaceous record. ZooKeys 465: 1-76. https://doi.org/10.3897/zookeys.465.8178
Temporal ranges of Cretaceous metatherian taxa used to calculate taxonomic richness of Metatheria.: Explanation note: Temporal ranges of Cretaceous metatherian taxa used to calculate taxonomic richness of Metatheria (Suppl. material 5). Data were compiled from the Paleobiology Database (PBDB; http: //fossilworks.org/?a=home), Kielan-Jaworowska et al. (2004), Woodburne et al. (2004), Williamson et al. (2012), Tables 3–4, and based on the timescale of Ogg et al. (2004).
Supplementary material 3 from: Williamson TE, Brusatte SL, Wilson GP (2014) The origin and early evolution of metatherian mammals: the Cretaceous record. ZooKeys 465: 1-76. https://doi.org/10.3897/zookeys.465.8178
Characters in common on the most parsimonious trees diagnosing the nodes on the strict consensus tree in Figure 6.: Explanation note: Characters in common on the most parsimonious trees diagnosing the selected nodes on the strict consensus tree resulting from the analysis run with characters ordered.
The beginning of a Wilson cycle in an accretionary orogen
<p>suporting data</p>
How stable are solar-type cycles over half a century? Chromospheric S-indices Mt. Wilson vs. TIGRE
<p> <br>by Klaus-Peter Schröder (1); Jürgen Schmitt (2); Marco Mittag (2)<br>Departamento de Astronomia, Universidad de Guanajuato, Mexico; Hamburger<br>Sternwarte, University of Hamburg, Germany</p> <p>Since autumn 2013, the robotic 1.2m telescope TIGRE (formerly the Hamburg Robotic<br>Telescope) is operating in Guanajuato (Mexico, and see poster by Gonzalez et al.). Regularly<br>using the same calibration stars for S-indices as did the Mount Wilson project (see Baliunas et<br>al. 1995), our R=20,000 HEROS echelle spectra have provided a decade of chromospheric<br>activity monitoring of the same ca. 100 solar-type stars, including a smaller number with<br>pronounced cycles (see Schröder et al. 2013) of periods of o(10yrs), which were already<br>observed at Mount Wilson since the 1970ies. Hence, on a timescale of half a century, we can<br>now use those same stars, first shown by Olin C. Wilson and his group to perform solar-type<br>activity cycles, to probe the stability of these cycles. This is motivated by the solar cycle<br>variability, which is evident, when comparing the last two, relatively weak maxima monitored by<br>TIGRE, with the Mount Wilson data from the 1970ies and 1980ies. Hence, we here show that<br>this is not a singular behavior. Strong cycles seem to be less variable, while weaker cycles like<br>the solar are natural to change between stronger and weaker performance. In the case of the<br>Sun this behavior is consistent with an o(century)-period as of the semi-regular Gleissberg<br>cycle, as well as with the occurrence of grand-minima.</p> <p><br>Theme(s): The Sun and Cool Stars in the Time Domain, Cool Stars as Stellar Systems</p>
FIGURE 21. Caligus bonito Wilson, 1905, female. A in The sea lice (Copepoda: Caligidae) of Moreton Bay (Queensland, Australia), with descriptions of thirteen new species
FIGURE 21. Caligus bonito Wilson, 1905, female. A, habitus, dorsal; B, antenna, post-antennal process and maxillule drawn in situ; C, brachium of maxilla; D, maxilliped; E, sternal furca; F, leg 1; G, endopod of leg 2, showing denticulate ornamentation on lateral margin of first and second segments; H, outer spines on exopod of leg 2. Scale bars: 1.0 mm on A, 200 µm on B–D, 100 µm on E–H.
FIGURE 15. Caligus aesopus Wilson, 1921, female. A in The sea lice (Copepoda: Caligidae) of Moreton Bay (Queensland, Australia), with descriptions of thirteen new species
FIGURE 15. Caligus aesopus Wilson, 1921, female. A, habitus, dorsal; B, antenna and post-antennal process, drawn in situ; C, maxilliped; D, sympod of leg 1, showing anterior process on ventral surface; E, leg 3; F, exopod of leg 4. Scale bars: 1.0 mm on A, 100 µm on B, D, 200 µm on C, E, F.
FIGURE 2. Alebion maculatus Wilson, 1932, male. A in The sea lice (Copepoda: Caligidae) of Moreton Bay (Queensland, Australia), with descriptions of thirteen new species
FIGURE 2. Alebion maculatus Wilson, 1932, male. A, habitus, dorsal; B, antenna, post-antennal process, maxillule and postoral process, drawn in situ; C, setal elements on distal margin of exopod of leg 1, showing modified spatulate spine 2; D, outer margin of exopod of leg 2 showing sexually dimorphic modified spines on segments 2 and 3; E, exopod of leg 3, showing modified spatulate outer spines on segments 2 and 3; F, endopod of leg 3; G, leg 5, ventral. Scale bars: 1.0 mm on A, 200 µm on B, E, F, 100 µm on D, 50 µm on C, G.
FIGURE 22. Caligus bonito Wilson, 1905, female. A in The sea lice (Copepoda: Caligidae) of Moreton Bay (Queensland, Australia), with descriptions of thirteen new species
FIGURE 22. Caligus bonito Wilson, 1905, female. A, exopod of leg 3; B, leg 4. Male, C, habitus, dorsal; D, post-antennal process; E, maxilliped. Scale bars: 100 µm on A, 200 µm on B, 1.0 mm on C, 250 µm on D–E.
FIGURE 18. Caligus ariicolus Wilson, 1928, female. A in The sea lice (Copepoda: Caligidae) of Moreton Bay (Queensland, Australia), with descriptions of thirteen new species
FIGURE 18. Caligus ariicolus Wilson, 1928, female. A, habitus, dorsal; B, antenna, post-antennal process and maxillule drawn in situ; C, maxilliped; D, sternal furca, showing adjacent accessory processes; E, leg 1; F, outer margin spines on exopod of leg 2; G, ornamentation on lateral margin of endopodal segments 1 and 2 of leg 2; H, leg 4. Scale bars: 1.0 mm on A, 200 µm on B, C, E, H, 100 µm on D, 50 µm on F, G.
Supplementary material 4 from: Magona N, Richardson DM, Le Roux JJ, Kritzinger-Klopper S, Wilson JRU (2018) Even well-studied groups of alien species might be poorly inventoried: Australian Acacia species in South Africa as a case study. NeoBiota 39: 1-29. https://doi.org/10.3897/neobiota.39.23135
Details of the forestry trial at Damara Farm, South Africa, that included many species of wattles not previously recorded from South Africa :
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