2,375 research outputs found

    Vekunta extima Yang et Wu

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    Vekunta extima Yang et Wu Vekunta extima Yang et Wu, 1993: 111, fig. 52. Distribution: Taiwan. Vekunta fera Yang et Wu Vekunta fera Yang et Wu, 1993: 128, fig. 61. Distribution: Taiwan. Vekunta flavipes Muir Vekunta flavipes Muir, 1922: 336. Distribution: India (Assam). Vekunta fuscolineata sp. nov. Distribution: Korea. Vekunta gracilenta Ya ng et Wu Vekunta gracilenta Yang et Wu, 1993: 119, fig. 56. Distribution: Taiwan. Vekunta hyalina Muir Vekunta hyalina Muir, 1913: 37, pl. 1, fig. 7. Distribution: Indonesia (Java). Vekunta intermedia Yang et Wu Vekunta intermedia Yang et Wu, 1993: 121, fig. 57. Distribution: Taiwan. Vekunta jahini sp. nov. Distribution: Korea. Vekunta kotoshonis Matsumura Vekunta kotoshonis Matsumura, 1940: 47; Yang et Wu, 1993: 100, fig. 46. Distribution: Taiwan. Vekunta lineata Melichar Vekunta lineata Melichar, 1914: 270; Melichar, 1915: 117. Distribution: Philippines. Vekunta lyricen Fennah Vekunta lyricen Fennah, 1956: 484, fig. 12 (female); Yang et Wu, 1993: 100, fig. 45 (male). Distribution: Taiwan. Vekunta maculata Matsumura Vekunta maculata Matsumura, 1914: 288; Schumacher, 1915 a: 121; Schumacher, 1915 b: 134; Liang et Wu, 1993: 109, fig. 50. Vekunta albipennis Muir, 1914: 44. Distribution: Taiwan. Vekunta makii Muir Vekunta makii Muir, 1914: 45; Schumacher, 1915 a: 121; Yang et Wu, 1993: 111, fig. 51. Distribution: Taiwan. Vekunta malloti Matsumura Vekunta malloti Matsumura, 1914: 288; Muir, 1915: 117; Schumacher, 1915 a: 120; Liang et Wu, 1993: 132, fig. 63. Vekunta okadae Muir, 1914: 45. Distribution: Japan (Honshu, Kyushu, Shikoku), Taiwan. Vekunta memoranda Ya n g et Wu Vekunta memoranda Yang et Wu, 1993: 104, fig. 48. Distribution: Taiwan. Vekunta nigra Ya n g et Wu Vekunta nigra Yang et Wu, 1993: 115, fig. 54. Distribution: Taiwan. Vekunta nigrolineata Muir Vekunta nigrolineata Muir, 1914: 44; Schumacher, 1915 a: 120; Matsumura, 1940: 47; Yang et Wu, 1993: 134, fig. 64. Distribution: Taiwan. Vekunta nitida (Bierman) Temesa nitida Bierman, 1910: 18, pl. 1, fig. 7. Vekunta nitida: Muir, 1926: 400. Distribution: Indonesia (Sumatra). Vekunta nivea Fennah Vekunta nivea Fennah, 1956: 482, fig. 12. Distribution: China (Zhejiang). Vekunta nutabunda Ya n g et Wu Vekunta nutabunda Yang et Wu, 1993: 117, fig. 55. Distribution: Taiwan. Vekunta obaerata Ya n g et Wu Vekunta obaerata Yang et Wu, 1993: 121, fig. 58. Distribution: Taiwan. Vekunta obliqua Ya ng et Wu Vekunta obliqua Yang et Wu, 1993: 124, fig. 59. Distribution: Taiwan. Vekunta palawanensis Muir Vekunta palawanensis Muir, 1917: 60. Distribution: Philippines (Palawan). Vekunta parca Yang et Wu Vekunta parca Yang et Wu, 1993: 113, fig. 53. Distribution: Taiwan. Vekunta pseudobadia Muir Vekunta pseudobadia Muir, 1915: 116. Distribution: Indonesia (Java, Sumatra). Vekunta punctula (Melichar) Temesa punctula Melichar, 1903: 41. Vekunta punctula: Distant, 1906 b: 288; Matsumura, 1914: 288; Schumacher, 1915 a: 120; Muir, 1923: 174. Distribution: Sri Lanka, Indonesia (Sumatra). Vekunta shirakii Matsumura Vekunta shirakii Matsumura, 1914: 289; Schumacher, 1915 a: 121; Yang et Wu, 1993: 134. Distribution: Taiwan. Vekunta stigmata Matsumura Vekunta stigmata Matsumura, 1914: 290; Schumacher, 1915 a: 121; Yang et Wu, 1993: 102, fig. 47. Vekunta ishidae Muir, 1914: 45. Distribution: Taiwan. Vekunta sublucida (Walker, 1870) Brixia sublucida Walker, 1870: 107. Vekunta sublucida: Liang, 2000: 235. Distribution: New Guinea. Vekunta tenella (Melichar) Temesa tenella Melichar, 1903: 41, pl. 3, fig. 11. Vekunta tenella: Distant, 1906 b, fig. 136. Distribution: Sri Lanka. Vekunta triprotrusa Wu et Liang Vekunta triprotrusa Wu et Liang, 2001: 515, figs. 20−31. Distribution: China (Yunnan). Vekunta umbripennis Muir Vekunta umbripennis Muir, 1914: 46; Schumacher, 1915 a: 121; Yang et Wu, 1993: 106, fig. 49. Distribution: Taiwan.Published as part of Rahman, Mohammad Atikur, Kwon, Yong Jung & Suh, Sang Jae, 2012, Two new species of the genus Vekunta Distant (Hemiptera: Fulgoromorpha: Derbidae) from Korea, pp. 23-33 in Zootaxa 3313 on pages 25-26, DOI: 10.5281/zenodo.21530

    Tomato Suspension Agreements and the Effects on Market Prices and Farm Revenue

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    The production capacity of the US tomato industry has decreased significantly in the past decade. The US Department of Commerce and the Mexican tomato industry negotiated and signed several Suspension Agreements that set floor prices for imported Mexican fresh tomatoes to protect the US domestic industry. This 4-page article written by Zhengfei Guan, Dong Hee Suh, and Feng Wu and published by the UF/IFAS Food and Resource Economics Department provides a review of the history of the suspension agreements and an analysis of their effects on the US tomato industry. http://edis.ifas.ufl.edu/fe102

    Tomato Suspension Agreements and the Effects on Market Prices and Farm Revenue

    No full text
    The production capacity of the US tomato industry has decreased significantly in the past decade. The US Department of Commerce and the Mexican tomato industry negotiated and signed several Suspension Agreements that set floor prices for imported Mexican fresh tomatoes to protect the US domestic industry. This 4-page article written by Zhengfei Guan, Dong Hee Suh, and Feng Wu and published by the UF/IFAS Food and Resource Economics Department provides a review of the history of the suspension agreements and an analysis of their effects on the US tomato industry. http://edis.ifas.ufl.edu/fe102

    Tomato Suspension Agreements and the Effects on Market Prices and Farm Revenue

    No full text
    The production capacity of the US tomato industry has decreased significantly in the past decade. The US Department of Commerce and the Mexican tomato industry negotiated and signed several Suspension Agreements that set floor prices for imported Mexican fresh tomatoes to protect the US domestic industry. This 4-page article written by Zhengfei Guan, Dong Hee Suh, and Feng Wu and published by the UF/IFAS Food and Resource Economics Department provides a review of the history of the suspension agreements and an analysis of their effects on the US tomato industry. http://edis.ifas.ufl.edu/fe102

    Endogonales in Taiwan: a new genus with unizygosporic sporocarps and a hyphal mantle

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    A new genus, Peridiospora, in the Endogonaceae was first extracted from the mountain area of National Yu-shan Park Central Taiwan mostly associated with Pieris taiwanensis. Peridiospora is characterized by producing only one zygospore in a zygosporocarp which is enclosed in a hyphal mantle. The genus accomodates two species, namely, P. tatachia, and P. reticulata. This is the first record of Endogonales in Taiwan. Keys to the genera in Endogonaceae and to the species of Peridiospora are provided

    Ultra-long, free-standing, single-crystalline vanadium dioxide micro/nanowires grown by simple thermal evaporation

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    Recently, it was discovered that single-crystalline VO2 nanostructures exhibit unique, single-domain metal-insulator phase transition. They enable a wide range of device applications as well as discoveries of oxide physics beyond those can be achieved with VO2 bulk or thin films. Previous syntheses of these nanostructures are limited in density, aspect ratio, single-crystallinity, or by substrate clamping. Here we break these limitations and synthesize ultra-long, ultra-dense, and free-standing VO2 micro/nanowires using a simple vapor transport method. These are achieved by enhancing the VO2 nucleation and growth rates using rough-surface quartz as the substrate and V2O5 powder as the evaporation source

    Vekunta albipennis Matsumura

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    Vekunta albipennis Matsumura Vekunta albipennis Matsumura, 1914: 289. Distribution: Taiwan. Vekunta angusta Wu et Liang Vekunta angusta Wu et Liang, 2001: 512, figs. 1−9. Distribution: India (S. Coorg). Vekunta asymmetrica Liang et Wu Vekunta asymmetrica Liang et Wu, 2001: 513, figs. 10−19. Distribution: China (Xizang). Vekunta atripennis Matsumura Vekunta atripennis Matsumura, 1940: 46. Distribution: Taiwan. Vekunta badia Muir Vekunta badia Muir, 1913: 38. Distribution: Borneo. Vekunta botelensis Matsumura Vekunta botelensis Matsumura, 1940: 46. Distribution: Taiwan. Vekunta bri Löcker, Löcker et Holzinger Vekunta bri Löcker, Löcker et Holzinger, 2009: 15, fig. 8. Distribution: Seychelles (Mahé, Silhouette). Vekunta commendata Ya n g et Wu Vekunta commendata Yang & Wu, 1993: 126, fig. 60. Distribution: Taiwan. Vekunta deducta (Walker) Cixius deductus Walker, 1857: 149. Vekunta deducta: Liang, 2000: 235. Distribution: Borneo. Vekunta despecta (Walker) Cixius despectus Walker, 1857: 148. Vekunta despecta: Liang, 2000: 235. Distribution: Borneo. Vekunta diluta Yang et Wu Vekunta diluta Yang et Wu, 1993: 130, fig. 62. Distribution: Taiwan.Published as part of Rahman, Mohammad Atikur, Kwon, Yong Jung & Suh, Sang Jae, 2012, Two new species of the genus Vekunta Distant (Hemiptera: Fulgoromorpha: Derbidae) from Korea, pp. 23-33 in Zootaxa 3313 on page 24, DOI: 10.5281/zenodo.21530

    Two-dimensional semiconductor alloys: Monolayer Mo1-xWxSe2

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    Monolayer Mo1-xWxSe2 (x = 0, 0.14, 0.75, and 1) alloys were experimentally realized from synthesized crystals. Mo1-xWxSe2 monolayers are direct bandgap semiconductors displaying high luminescence and are stable in ambient. The bandgap values can be tuned by varying the W composition. Interestingly, the bandgap values do not scale linearly with composition. Such non-linearity is attributed to localization of conduction band minimum states around Mo d orbitals, whereas the valence band maximum states are uniformly distributed among W and Mo d orbitals. Results introduce monolayer Mo1-xWxSe2 alloys with different gap values, and open a venue for broadening the materials library and applications of two-dimensional semiconductors

    Formation and stability of point defects in monolayer rhenium disulfide

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    Abstract: Recently, rhenium disulfide (ReS2) monolayers were experimentally extracted by conventional mechanical exfoliation technique from as-grown ReS2 crystals. Unlike the well-known members of transition metal dichalcogenides (TMDs), ReS2 crystallizes in a stable distorted-1T structure and lacks an indirect to direct gap crossover. Here we present an experimental and theoretical study of the formation, energetics, and stability of the most prominent lattice defects in monolayer ReS2. Experimentally, irradiation with 3-MeV He+2 ions was used to break the strong covalent bonds in ReS2 flakes. Photoluminescence measurements showed that the luminescence from monolayers is mostly unchanged after highly energetic a particle irradiation. In order to understand the energetics of possible vacancies in ReS2 we performed systematic first-principles calculations. Our calculations revealed that the formation of a single sulfur vacancy has the lowest formation energy in both Re and S rich conditions and a random distribution of such defects are energetically more preferable. Sulfur point defects do not result in any spin polarization whereas the creation of Re-containing point defects induce magnetization with a net magnetic moment of 1-3 mu B. Experimentally observed easy formation of sulfur vacancies is in good agreement with first-principles calculations
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