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471 results for “Soares”
FIGURE 5 in Three new species of Thrasychiroides Soares & Soares, 1947 from Brazilian Mountains (Opiliones, Eupnoi, Neopilionidae)
FIGURE 5. Penes of Thrasychiroides species. A–C. T. brasilicus, A. dorsal view; B. lateral view; C. ventral view. D–F. T. moporanga sp. nov., D. dorsal view; E. lateral view; F. ventral view. G–I. T. toryba sp. nov., G. dorsal view; H. lateral view; I. ventral view. J–L. T. ybytyra sp. nov., J. dorsal view; K. lateral view; L. ventral view. Scale bars = 0.05 mm. Labels. 1= stylus; 2= glans; 3= arms; 4= shaft; 5= spine on shoulder.
FIGURE 7 in Three new species of Thrasychiroides Soares & Soares, 1947 from Brazilian Mountains (Opiliones, Eupnoi, Neopilionidae)
FIGURE 7. Penis of the holotype of Thrasychirus gulosus (MZSP 56030) A. dorsal view; B. ventral view. C. lateral view. Scale bars = 0.1 mm.
FIGURE 8 in Three new species of Thrasychiroides Soares & Soares, 1947 from Brazilian Mountains (Opiliones, Eupnoi, Neopilionidae)
FIGURE 8. Strict consensus cladogram (338 steps, consistence index 0.28, retention index 0.64) showing the relationships among Enantiobuninae genera. For character description see Taylor (2011). For characters changed or added for Thrasychirus gulosus, Thrasychiroides brasilicus and the three new species of Thrasychiroides see Appendix 1.
FIGURE 1 in Three new species of Thrasychiroides Soares & Soares, 1947 from Brazilian Mountains (Opiliones, Eupnoi, Neopilionidae)
FIGURE 1. Dorsal and lateral views of the holotypes of the new Thrasychiroides species. A–B. T. moporanga sp. nov., dorsal and lateral view, respectively; C–D. T. toryba sp. nov., dorsal and lateral view, respectively; E–F. T. ybytyra sp. nov., dorsal and lateral view, respectively. Scale bars = 0.5 mm.
FIGURE 4 in Three new species of Thrasychiroides Soares & Soares, 1947 from Brazilian Mountains (Opiliones, Eupnoi, Neopilionidae)
FIGURE 4. Photographs of the male holotype of Thrasychiroides ybytyra sp. nov. A. dorsal view; B. lateral view; C. chelicera and pedipalp details. Scale bars = 1 mm.
FIGURE 3 in Three new species of Thrasychiroides Soares & Soares, 1947 from Brazilian Mountains (Opiliones, Eupnoi, Neopilionidae)
FIGURE 3. Photographs of the male holotype of Thrasychiroides toryba sp. nov. A. dorsal view; B. lateral view; C. chelicera and pedipalp details. Scale bars = 1 mm.
FIGURE 6 in Three new species of Thrasychiroides Soares & Soares, 1947 from Brazilian Mountains (Opiliones, Eupnoi, Neopilionidae)
FIGURE 6. Tips of penial glans of the holotypes of Thrasychiroides species. A–B. T. brasilicus.. C–D. T. moporanga sp. nov. E–F. T. toryba sp. nov. G–H. T. ybytyra sp. nov. Upper row: ventral view; Bottom row: dorsal view. Scale bars = 0.05 mm.
FIGURE 2 in Three new species of Thrasychiroides Soares & Soares, 1947 from Brazilian Mountains (Opiliones, Eupnoi, Neopilionidae)
FIGURE 2. Photographs of the male holotype of Thrasychiroides moporanga sp. nov. A. dorsal view; B. lateral view; C. chelicera details; D. pedipalp tibia details. Scale bars = 1 mm.
Groping in the fog: Soaring migrants exhibit wider scatter in flight directions and respond differently to wind under low visibility conditions
<p>Atmospheric conditions are known to affect flight propensity, behaviour during flight, and migration route in birds. Yet, the effects of fog have only rarely been studied although they could disrupt orientation and hamper flight. Fog could limit the visibility of migrating birds such that they might not be able to detect landmarks that guide them during their journey. Soaring migrants modulate their flight speed and direction in relation to the wind vector to optimise the cost of transport. Consequently, landmark-based orientation, as well as adjustments of flight speed and direction in relation to wind conditions, could be jeopardised when flying in fog. Using a radar system operated in a migration bottleneck (Strait of Messina, Italy), we studied the behaviour of soaring birds under variable wind and fog conditions over two consecutive springs (2016 and 2017), discovering that migrating birds exhibited a wider scatter of flight directions and responded differently to wind under fog conditions. Birds flying through fog deviated more from the mean migration direction and increased their speed with increasing crosswinds. In addition, airspeed and groundspeed increased in the direction of the crosswind, causing the individuals to drift laterally. Our findings represent the first quantitative empirical evidence of flight behaviour changes when birds migrate through fog and explain why low visibility conditions could risk their migration journey.</p>
FIGURES 21–26 in Soares testudinarius gen. et sp. nov. (Hemiptera: Fulgoromorpha: Flatidae), a new representative of the tribe Phantiini from Madagascar
FIGURES 21–26. Soares testudinarius gen. et sp. n., female. (21) anterior part of body, lateral view; (22) frons, anterior view; (23) same, latero-ventral view; (24) habitus, ventral view; (25) frons, ventral view; (26) rostrum, ventral view. (21–23 holotype, 24–26 paratype).
FIGURES 39–44 in Soares testudinarius gen. et sp. nov. (Hemiptera: Fulgoromorpha: Flatidae), a new representative of the tribe Phantiini from Madagascar
FIGURES 39–44. Soares testudinarius gen. et sp. n., female. (39) anal tube, lateral view; (40) same, dorso-lateral view; (41) same, dorsal view; (42) genital capsule, ventral view; (43) gonoplac, ventral view; (44) surface of gonoplac. (39–41 holotype, 42–44 paratype).
FIGURES 9–14 in Soares testudinarius gen. et sp. nov. (Hemiptera: Fulgoromorpha: Flatidae), a new representative of the tribe Phantiini from Madagascar
FIGURES 9–14. Soares testudinarius gen. et sp. n., female, holotype. (9) habitus, dorsal view; (10) anterior part of body, dorsal view, (11) habitus, lateral view; (12–13) anterior part of body, dorso-lateral view; (14) vertex and pronotum, dorso-lateral view.
FIGURES 15–20 in Soares testudinarius gen. et sp. nov. (Hemiptera: Fulgoromorpha: Flatidae), a new representative of the tribe Phantiini from Madagascar
FIGURES 15–20. Soares testudinarius gen. et sp. n., female. (15) anterior part of body, dorso- anterior view; (16–17) sensory and wax pores on vertex, dorsal view; (18) antenna, ventral view; (19) same, dorsal view; (20) top of antenna with antennal plate organs. (15, 18–20 holotype, 16–17 paratype).
FIGURES 33–38 in Soares testudinarius gen. et sp. nov. (Hemiptera: Fulgoromorpha: Flatidae), a new representative of the tribe Phantiini from Madagascar
FIGURES 33–38. Soares testudinarius gen. et sp. n., female. (33) habitus, lateral view; (34) hind wing, lateral view; (35) hind leg; (36) hind tibia and tarsomeres, ventral view; (37) lateral spine of tibia, ventral view; (38) distal part of tibia and tarsomeres, ventral view. (33–34 holotype, 35–38 paratype).
FIGURES 27–32 in Soares testudinarius gen. et sp. nov. (Hemiptera: Fulgoromorpha: Flatidae), a new representative of the tribe Phantiini from Madagascar
FIGURES 27–32. Soares testudinarius gen. et sp. n., female. (27) tegmen, dorsal view with focus on median part; (28) same, focus on anterior part; (29) same, focus on clavus; (30) anterior part of tegmina; (31) dorsal part of tegmina; (32) wax glandplates on tegmen. (27–28, 30, 32 holotype, 29, 31 paratype).
The interplay of wind and uplift facilitates over-water flight in facultative soaring birds
<p class="western"><span>Flying over the open sea is energetically costly for terrestrial birds. Despite this, over-water journeys of many birds, sometimes hundreds of kilometers long, are uncovered by bio-logging technology. To understand how these birds afford their flights over the open sea, we investigated the role of atmospheric conditions, specifically wind and uplift, in subsidizing over-water flight at the global scale. We first established that ∆<i>T</i>, the temperature difference between sea surface and air, is a meaningful proxy for uplift over<span> water</span>. Using this proxy, we showed that the spatio-temporal patterns of sea-crossing in terrestrial migratory birds is associated with favorable uplift conditions. We then analyzed route selection over the open sea for <span>five</span> facultative soaring species, representing all major migratory flyways. The birds maximized wind support when selecting their sea-crossing routes and selected higher uplift when suitable wind support<span> was</span> available.<span> They also preferred routes with low long-term uncertainty in wind conditions. </span>Our findings suggest that, in addition to wind, uplift may play a key role in the energy seascape for bird migration that in turn determines strategies and associated costs for birds crossing ecological barriers such as the open sea.</span></p>
High-resolution modelling of uplift landscapes can inform micro-siting of wind turbines for soaring raptors
<p>Collision risk of soaring birds is partly associated with updrafts to which they are attracted. To identify risk-enhancing landscape features, a micro-siting tool was developed to model orographic and thermal updraft velocities from high-resolution remote sensing data. The tool was applied to the island of Hitra, and validated using GPS-tracked white-tailed eagles (<i>Haliaeetus albicilla</i>). Resource selection functions predicted that eagles preferred ridges with high orographic uplift, especially at flight altitudes within the rotor-swept zone (40-110 m). Flight activity was negatively associated with the widely distributed areas with high thermal uplift at lower flight altitudes (<110 m). Both the existing wind-power plant and planned extension are placed at locations rendering maximum orographic updraft velocities around the minimum sink rate for white-tailed eagles (0.75 m/s) but slightly higher thermal updraft velocities. The tool can contribute to improved micro-siting of wind turbines to reduce environmental impacts, especially for soaring raptors.</p>
CDMF Pesquisa - Leandro Luiz Soares
<p>Leandro Luiz Soares, doutorando no Programa de Pós-Graduação em Química da Universidade Federal de São Carlos (PPGQ - UFSCar) e integrante do Centro de Desenvolvimento de Materiais Funcionais (CDMF), fala de sua pesquisa com materiais a base de perovskita para aplicação em dispositivos fotovoltaicos.</p> <p>CDMF Pesquisa - Leandro Luiz Soares de <a href="https://youtu.be/RBQUtVyUEAY">https://youtu.be/RBQUtVyUEAY</a> está licenciado com uma Licença <a href="http://creativecommons.org/licenses/by-nc-nd/4.0/">Creative Commons - Atribuição-NãoComercial-SemDerivações 4.0 Internacional</a>. Podem estar disponíveis autorizações adicionais às concedidas no âmbito desta licença em <a href="https://www.labi.ufscar.br/">https://www.labi.ufscar.br/</a>.</p>
CDMF Pesquisa - Jussara Soares da Silva
<p> </p> <p>Jussara Soares da Silva, doutoranda no Programa de Pós Graduação em Química da Universidade Federal de São Carlos (PPGQ - UFSCar) e pesquisadora do Centro de Desenvolvimento de Materiais Funcionais da Universidade Federal de São Carlos (CDMF -UFSCar), fala de suas pesquisas voltadas ao estudo das propriedades bactericidas e luminescentes dos decorados de hidroxiapatita com vanadato de prata.</p> <p>CDMF Pesquisa - Jussara Soares da Silva de <a href="https://youtu.be/-QBntt_tpwE">https://youtu.be/-QBntt_tpwE</a> está licenciado com uma Licença <a href="http://creativecommons.org/licenses/by-nc-nd/4.0/">Creative Commons - Atribuição-NãoComercial-SemDerivações 4.0 Internacional</a>. Podem estar disponíveis autorizações adicionais às concedidas no âmbito desta licença em <a href="https://www.labi.ufscar.br/">https://www.labi.ufscar.br/</a>.</p>
CDMF Pesquisa - Marianna Soares de Jesus Godoi
<p>Marianna Soares de Jesus Godoi, aluna de Iniciação Científica no Centro de Tecnologia da Informação Renato Archer (CTI) e integrante do Centro de Desenvolvimento de Materiais Funcionais (CDMF), fala de sua pesquisa sobre o desenvolvimento de imunossensor para diagnóstico da Dengue.</p> <p>CDMF Pesquisa - Marianna Soares de Jesus Godoi de <a href="https://youtu.be/78EQe1hMCYM">https://youtu.be/78EQe1hMCYM</a> está licenciado com uma Licença <a href="http://creativecommons.org/licenses/by-nc-nd/4.0/">Creative Commons - Atribuição-NãoComercial-SemDerivações 4.0 Internacional</a>. Podem estar disponíveis autorizações adicionais às concedidas no âmbito desta licença em <a href="https://www.labi.ufscar.br/">https://www.labi.ufscar.br/</a>.</p>
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