3,581 research outputs found
Letter from Ohashi to Jack Noda, March 18, 1942
No full textLetter from Mr. Ohashi of the Stockton chapter of the Japanese American Citizens League to Jack Noda, president of the Stanislaus Merced chapter of the Japanese American Citizens League regarding the Stockton chapter's constitution.The Nisaburo Aibara Collection features materials from the Turlock Social Club, a local Japanese-American community group active between 1939 and 1970. It contains documents regarding the Stockton, Turlock and Merced Assembly Centers and Japanese American Citizens League chapters. The Collection also features correspondences with reactions, responses, and preparations for the forced evacuation. Additionally, the Collection has records on the Central California Cantaloupe Company, Turlock Farm Corporation, Turlock Japanese Society, and family records and funeral service programs of Japanese-American residents of Turlock
Letter from Ohashi to Jack Noda, March 20, 1942
No full textFollow-up letter from Mr. Ohashi of the Stockton chapter of the Japanese American Citizens League to Jack Noda, president of the Stanislaus Merced chapter of the Japanese American Citizens League regarding the Stockton chapter's constitution and the mass removal preparation.The Nisaburo Aibara Collection features materials from the Turlock Social Club, a local Japanese-American community group active between 1939 and 1970. It contains documents regarding the Stockton, Turlock and Merced Assembly Centers and Japanese American Citizens League chapters. The Collection also features correspondences with reactions, responses, and preparations for the forced evacuation. Additionally, the Collection has records on the Central California Cantaloupe Company, Turlock Farm Corporation, Turlock Japanese Society, and family records and funeral service programs of Japanese-American residents of Turlock
Pleurolobus flexuosus H. Ohashi & K. Ohashi 2018
No full text1. <i>Pleurolobus flexuosus</i> (Wallich 1831: 195 ex Bentham 1852: 224) H.Ohashi & K. Ohashi (2018c: 386). <p> <i>≡</i> <i>Desmodium flexuosum</i> Wall. ex Benth.</p> <p> Type:— MYANMAR. Montes Prome, 1826, <i>Wallich 5691</i> (lectotype K-W! K001121777, designated here, isolectotypes G!-2 sheets, BM!, K! K000858866, CAL, <i>n.v.</i>).</p> <p> <i>≡</i> <i>Meibomia flexuosa</i> (Wall. ex Benth.) Kuntze (1891: 198).</p> <p> Creeping herb; stems and twigs angular or subterete, brown pubescent. <i>Leaves</i> subalternately or spirally arranged; stipules, narrowly triangular, 5–10 × 1–1.5 mm, apex acuminate, surface long pubescent; petioles (0.3–) 1.5–3.5 cm long, densely erect pubescent. <i>Leaflet</i> coriaceous; stipels narrowly triangular to filiform, 2–5 mm long, apex pointed, surface glabrescent to pubescent; petiolules 1–3 mm, densely pubescent; leaf blade cordate, broadly obovate to broadly elliptic, 1.5–6.5 × 1.5–6 cm, apex ±acute to rounded or shallowly emarginate, base ±cordate, margin entire, upper surface glabrescent, lower surface appressed pubescent, denser than upper surface; lateral veins 7–9 per side. <i>Inflorescences</i> pseudoracemose or paniculate, with a few branches, 5–15 cm long; rachis and rachilla densely pubescent and minutely uncinate. <i>Primary bract</i> 3–7 × 0.5 mm, apex pointed, surface long pubescent, enclosing 2-immature flowers and secondary bract. <i>Secondary bract</i> persistent, narrowly triangular, ca. 1 × 0.3 mm, pubescent. <i>Flowers</i> 2–2.5 mm long, 2-flowered fascicles; pedicels 2–2.5 mm long, with uncinate hairs. <i>Calyx</i> 1.5–2 mm long, base obtuse; outside white pubescent, tube ca. 1 mm long; teeth 4, 0.8–1 mm long, ±equal to tube length, upper tooth shallowly divided, less than 0.2 mm long. <i>Corolla</i>: standard broadly obovate, ca. 3 × 3 mm, apex shallowly emarginate, base attenuate, entire or slightly auriculate at base, claw very short; wings ca. 3 × 1.2 mm, ±equal to the keel petals, apex obtuse, base not auriculate, claw ca. 0.5 mm long; keels curved, ca. 3.2 × 1.5 mm, the broadest part near the apex, apex obtuse, base not auriculate, claw ca. 1.5 mm long. <i>Stamens</i> ca. 3 mm long. <i>Gynoecium</i> ca. 3.5 mm long; ovary appressed pubescent; style ca. 1.5 mm long, glabrescent; stigma minutely capitate. <i>Pods</i> dark brown to black, 3–4-articulate, straight, 7–10 × 2–2.5 mm, surface sparsely uncinate, inconspicuously reticulate-patterned, upper suture undulate, lower suture more constricted than upper suture, ca. 1 mm deep; isthmus 2/5 as broad as the pod; articles obliquely ovate or subcircular, ca. 3 mm long; pod usually sessile or shortly stipitate, ca. 0.5 mm long; fruiting pedicels 2.5–3 mm long, with uncinate hairs. <i>Seeds</i> transversely elliptic.</p> <p> <b>Distribution</b>:— Myanmar, Thailand, and Cambodia.</p> <p> <b>Ecology</b>:—In teak plantation, with bamboo and deciduous forests; 30–400 m elev.</p> <p> <b>Phenology</b>:—Flowering in November. Fruiting in November–February.</p> <p> <b>Notes</b>:— Two specimens, <i>Maxwell 06-874</i> (CMUB) and <i>Pierre 1006</i> (P) are newly recorded for Cambodia. <i>Desmodium flexuosum</i> Wall. ex Benth. was validly published. Five original specimens were examined at BM, G, K, and K-W by authors and one duplicate was recorded by Ohashi (1973). All specimens are from the same gathering and in a perfect condition. A specimen kept at K-W (K001121777) is selected here as the lectotype because it is well preserved in Wallich’s collection at Kew.</p> <p> <b>Specimens examined</b>:— <b>THAILAND.</b> Chiang Mai: Doi Suthep, 1100 m, 17 Oct. 1910, <i>Kerr 1480</i> (ABD, BM, C, K-2 sheets, L, P), Doi Suthep, 1200 m, 28 Nov. 1911, <i>Kerr 1480B</i> (BM, E, K, L, P) & Doi Suthep-Pui National Park, 350 m, 19 Dec. 1989, <i>Maxwell 89-1568</i> (CMU, E, L); Lampang: Chae Son, Ban Sa, 400 m, 7 Nov. 2008, <i>Maxwell 08-198</i> (CMUB); <b>CAMBODIA.</b> Kratie: Sambour, Mekong River, 30 m, 15 Nov. 2006, <i>Maxwell 06-874</i> (CMUB) & May 1870, <i>Pierre 1006</i> (G, P).</p>Published as part of <i>Saisorn, Witsanu & Chantaranothai, Pranom, 2022, A taxonomic revision of two genera, Pleurolobus and Sohmaea (Leguminosae) in Thailand and Indo-China, pp. 231-246 in Phytotaxa 573 (2)</i> on pages 232-233, DOI: 10.11646/phytotaxa.573.2.4, <a href="http://zenodo.org/record/7349951">http://zenodo.org/record/7349951</a>
Non-Abelian vortices with product moduli
No full textVortices of a new type, carrying non-Abelian flux moduli CP(n-1)xCP(r-1), are found in the context of softly broken N=2 supersymmetric quantum chromodynamics. By tuning the bare quark masses appropriately, we identify the vacuum in which the underlying SU(N) gauge group is partially broken to SU(n)xSU(r)xU(1)/Z(K), where K is the least common multiple of (n,r), and with N(f)(su(n))=n and N(f)(su(r))=r flavors of light quark multiplets. At much lower energies, the gauge group is broken completely by the squark vacuum expectation values, and vortices develop which carry non-Abelian flux moduli CP(n-1)xCP(r-1). For n > r, at the length scale at which the SU(n) fluctuations become strongly coupled and Abelianize, the vortex still carries weakly fluctuating SU(r) flux moduli. We discuss the possibility that these vortices are related to the light non-Abelian monopoles found earlier in the fully quantum-mechanical treatment of 4D supersymmetric quantum chromodynamics
Schizotetranychus gilvus Ehara & Ohashi 2005, sp. nov.
No full textSchizotetranychus gilvus sp. nov. (Japanese name: Kotomatahadani) (Figs. 1–16) Diagnosis — This species is distinct from any other known members of the genus in having tibiae I and II with 9 and 8 tactile setae, respectively, and the aedeagus with somewhat triangular shaft and conspicuous pickshaped terminal knob. It resembles S. zhangi Wang & Cui, 1992 which is known only from females collected in Yunnan, China, on Quercus gilliana Rehder & E.H. Wilson. However, the female of S. gilvus sp. nov. differs from that of S. zhangi in the following points: 1) Tibia II with 8 tactile setae (7 tactile setae in zhangi). 2) Each empodium with 2 dorsal appendant hairs on each of clawlike parts (1 dorsal appendant hair in zhangi). 3) Area immediately anterior to genital flap with longitudinal to curved striae (transverse striae in zhan g i). Female — Body greenish yellow in color, with 2 dark lateral spots on each side. Rostrum reaching middle to distal end of genu I (Fig. 1). Palpus with spinneret about twice as long as broad; dorsal sensillum (solenidion) rodlike, with subparallel sides (Fig. 2). Peritreme L or Ushaped distally (Fig. 5). Dorsolateral opisthosomal setae (c2 to f2) much longer than dorsocentral opisthosomals (c1 to h1); humeral seta (c3) very long, approximately 3 times the length of c1; each of c1 to f1 shorter than distance to base of seta next behind (Fig. 1). Opisthosomal striae on dorsocentral region transverse, with lobes approximately semicircular. Genital flap with transverse striae; area immediately anterior to flap with longitudinal to curved striae. Numbers of setae and solenidia (in parentheses) on leg segments: coxae 2–2–1–1, trochanters 1–1–1–1, femora 9–7–4–4, genua 5–5–3–3, tibiae 9(1)–8–6–7, tarsi 14(1)+ 2 dupl.–12(1)+ 1 dupl.–9(1)–9(1). Tarsus I with 5 tactile setae proximal to proximal set of duplex setae, and 1 solenidion near level of proximal duplex set (Fig. 9); tarsus II with 2 tactile setae and 1 solenidion proximal to duplex setae (Fig. 10). Empodia with 2 dorsal appendant hairs on each clawlike part; the upper dorsal appendant much shorter than the lower (Figs. 13–14). Measurements (mean, n=10): length of body (including rostrum) 526, width of body 284; lengths of setae (mean±SE): v2 53.6±0.7, sc1 52.0±0.5, sc2 67.4±1.0, c1 40.5±0.3, c2 55.7±0.7, c3 97.3±1.4, d1 39.3±0.3, d2 55.1±0.6, e1 39.6 ±0.5, e2 62.2±0.9, f1 40.4±1.1, f2 57.6±0.8, h1 53.8±1.2. Male — Color similar to female. Palpus with spinneret subconical, variable in shape; doral sensillum very slender, subparallelsided (Figs. 3–4). Aedeagus with shaft somewhat triangular, the dorsal and ventral margins nearly straight; terminal knob pickshaped, about 4.0 long; anterior projection of knob very small, acute; the posterior projection elongate, gently tapering; axis of knob forming slight angle with dorsal margin of shaft (Figs. 6–8). Numbers of setae and solenidia (in parentheses) on leg podomeres: coxae 2–2–1–1, trochanters 1–1–1–1, femora 9–7–4–4, genua 5–5–3–3, tibiae 9(3)–8[rarely 7]–6–7, tarsi 13(3)+2 dupl.–12(1)+1 dupl.–9(1)–9(1). Tarsus I with 4 tactile setae and 2 solenidia proximal to proximal set of duplex setae, and 1 solenidion near level of proximal duplex set (Fig. 11); tarsus II with 2 tactile setae and 1 solenidion proximal to duplex setae (Fig. 12). Empodium I with 1 or 2 dorsal and 1 ventral appendant hairs on each clawlike part (Figs. 15–16). Empodia II–IV similar to those of female. Measurements (mean, n=10): length of body (including rostrum) 437 (425); lengths of setae (mean±SE): v2 40.1±0.6 (37.9), sc1 38.7±0.8 (37.3), sc2 49.2±0.7 (48.0), c1 31.3±0.6 (28.0), c2 44.5±1.5 (38.7), c3 73.2±1.2 (74.3), d1 32.1±0.7 (30.6), d2 43.9±1.1 (38.7), e1 30.7 ±0.6 (27.7), e2 39.7 ±1.3 (33.8), f1 30.0±0.7 (28.4), f2 32.8±0.7 (31.6), h1 27.8±0.7 (26.5). Type series — Holotype: male (NSMTAc 11888), Botanical Garden of Kyoto University, Sakyoku, Kyoto, Honshu, Japan, 7X2004 (K. Ohashi leg.), on Quercus gilva Blume (Fagaceae). Paratypes: 4 males (NSMTAc 11889–11892), data same as for holotype; 1 male (NSMTAc 11893) and 3 females (NSMTAc 11894), 14IX2004, other data same as for holotype; 4 females (NSMTAc 11895–11896), Kitauoyanishimachi, Nara, Honshu, 18IX2004, other data same as for holotype; 2 males and 2 females (KUM), Takabatakecho, Nara, 18IX2004, other data same as for holotype. Other specimens — Six males and 6 females (Ehara’s private collection), Matsugasakihashikamicho, Sakyoku, Kyoto, 27III2004 (K. Ohashi leg.), on Q. gilva. Etymology — The specific name is taken from the Latin adjective gilvus meaning “pale yellow” or “yellowish”, referring to the body color.Published as part of Ehara, Shôzô & Ohashi, Kazunori, 2005, A new spider mite species of Schizotetranychus (Acari: Prostigmata: Tetranychidae) from Quercus gilva in Japan, pp. 1-5 in Zootaxa 884 (1) on pages 2-5, DOI: 10.11646/zootaxa.884.1.1, http://zenodo.org/record/504430
Sohmaea diffusa H. Ohashi & K. Ohashi 2018
No full text1. <i>Sohmaea diffusa</i> (DC. 1825a: 100) H.Ohashi & K.Ohashi (2018b: 161). <p> <i>≡</i> <i>Desmodium diffusum</i> DC.</p> <p> Type:— India orient, <i>Lambert s.n.</i> (lectotype G-DC! G00317409, designated by Ohashi & Xiang-Yun, 2005).</p> <p> <i>≡</i> <i>Hedysarum diffusum</i> [Roxburgh (1814: 57), <i>nom. nud.</i>] Roxburgh (1832: 357), <i>non</i> Willdenow (1802: 1180), <i>nom. illeg.</i> Type:— India orient, <i>Roxburgh s.n.</i> (syntypes BM, n.v. & BR! BR0000009894365 [digital image]).</p> <p> <i>=</i> <i>Desmodium laxiflorum</i> DC. var. <i>formosense</i> Ohwi (1951: 235). Type:— TAIWAN (Formosa). Fujieda in Kizangun, <i>Okamoto s.n.</i> (holotype KYO, n.v.), <i>fide</i> Ohashi & Zhu (2005).</p> <p> <i>=</i> <i>Desmodium laxiflorum</i> subsp. <i>parvifolium</i> H.Ohashi & T.T.Chen (1983: 268). Type:— TAIWAN. Pingtung Co., Mutan, 350–400 m, 26 Oct. 1982, <i>Ohashi et al. 13486</i> (holotype TUS, n.v., isotypes TAI, n.v., TI, n.v., TUS, n.v.), <i>fide</i> Ohashi & Zhu (2005).</p> <p> <i>=</i> <i>Desmodium unibotryosum</i> C.Chen & X.J. Cui (1987: 307), <i>nom. illeg.</i></p> <p> Herb, 10–70 cm high; stems and twigs terete, glabrescent or appressed pubescent. <i>Leaves</i> trifoliolate, rarely unifoliolate on lower part of plant, spirally arranged; stipules triangular, 3–10 × 2–3.5 mm, apex long acuminate, curved or straight, surface glabrescent to puberulous; petioles (0.3–) 1.5–2.5 cm long, appressed pubescent and uncinate; rachis 3–10 mm, appressed pubescent and uncinate. <i>Leaflets</i>: stipels filiform, 1.5–3 mm long, apex pointed, glabrescent; petiolules 1.5–2 mm long, pubescent. <i>Terminal leaflet</i> ±elliptic to obovate, 1.5–6.5 × 1–3.5 cm, apex acute to attenuate, base cuneate to obtuse, margin entire, upper surface sparsely straight and uncinate hairy, lower surface densely pubescent; lateral veins 5–7 per side, prominent. <i>Lateral leaflets</i> ±elliptic to ovate, 1–3.5 × 0.5–2 cm, apex acute, base obtuse, margin entire, both upper and lower surfaces like terminal leaflet; lateral veins 5–7 per side, prominent. <i>Inflorescences</i> 10–20 cm long, terminal at both terminal and lateral shoots; rachis straight and uncinate hairy. <i>Primary bract</i> narrowly ovate, ca. 3 × 0.7 mm, apex long acuminate, margin fimbriate, surface pubescent, distinctly veined, enclosing 4-immature flowers and secondary bract. <i>Secondary bract</i> narrowly ovate, 2–2.8 × 0.3–0.5 mm, margin fimbriate, surface pubescent. <i>Flowers</i> ca. 5 mm long, 4-flowered fascicles; bracteoles absent; pedicels 3–4 mm long, with straight hairs on lower most and densely uncinate hairs toward the upper part of pedicel. <i>Calyx</i> dark brownish red, 2.5–3 mm long, base obtuse; outside pubescent, inside glabrous, tube ca. 1.2 mm long; teeth 1–1.2 mm long, ±equal to tube length, upper tooth shallowly divided, ca. 0.3 mm deep. <i>Corolla</i>: standard light blue, wings and keels white; standard broadly ovate, 5.5–6 × 4–4.5 mm, apex emarginate, base attenuate to cuneate, entire at base, claw 1–1.7 mm long; wings slightly oblong to obovate, 4.5–5 × 1.5–2 mm, apex obtuse to rounded, base auriculate, 0.2–0.4 mm long, claw 0.5–0.8 mm long; keels narrowly curved, 4.5–5 × 1.3–1.5 mm, apex acute to obtuse, base auriculate, ca. 0.2 mm long, claw 1–1.8 mm long. <i>Stamens</i> 4.5–5 mm long; anthers ellipsoid, ca. 0.3 × 0.2 mm. <i>Gynoecium</i> 4.5–5 mm long; ovary oblong, sessile, laterally compressed, with minutely hairs, 6–8-ovulate; style 1.5–2 mm long, glabrescent; stigma minutely capitate. <i>Pods</i> indehiscent, 6–8-articulate, oblong, 3–3.5 × 0.2 cm, surface densely uncinate, smooth, upper and lower sutures repand, equally constricted, less than 0.5 mm deep; isthmus ca. 3/5 as broad as the pod; articles linear-oblong, 4–6 mm long, prominently longer than broad; pod stipe ca. 1.5 mm long, glabrescent; fruiting pedicels 3–4 mm long, pubescent, with straight hairs on lower most and densely uncinate hairs toward the apex. <i>Seeds</i> transversely oblong.</p> <p> <b>Distribution</b>:— India, Nepal, Bhutan, Myanmar, China, Taiwan, Thailand, Indonesia, Philippines, and Papua New Guinea.</p> <p> <b>Ecology</b>:—Open areas of deciduous and bamboo forests; ca. 635 m elev.</p> <p> <b>Phenology</b>:—Flowering in September–October. Fruiting in October–November.</p> <p> <b>Specimens examined:—</b> <b>THAILAND.</b> Chiang Mai: Mae Rim, Doi Suthep, 1 Oct. 1988, <i>Maxwell 88-1161</i> (CMU, L), Samoeng, Karen village, 11 Oct. 2001, <i>Maxwell 01-522</i> (CMUB) & Mae Rim, Mae Sa Botanical Garden, 5 Oct. 1989, <i>Pooma 372</i> (BKF); Nan: Doi Phu Kha, 31 Oct. 2013, <i>Clark et al. 303</i> (K); <b>LAOS.</b> Houa Phan: Na Ham, Sam Neua, 14 Sept. 1920, <i>Poilane 1851</i> (AAU, BKF, L, P-2 sheets); Entre N. Dlet et M. Seng Traminh, 800–1000 m, 13 Sept. 1929, <i>Poilane 16940</i> (P); 240 Km de la route de Vinh au Tanninh, 1500–1600 m, 30 Aug. 1929, <i>Poilane 16790</i> (P-2 sheets); <b>VIETNAM.</b> Tonkin: Moc Ha, 10 Oct. 1891, <i>Balansa 4493</i> (P), without locality, Oct. 1887, <i>Balansa 2205</i> (P), Tonkin Occidental, <i>Bon 6070</i> (P-2 sheets), Tonkin Occidental, <i>Bon 6071</i> (P-2 sheets) & Tonkin Occidental, <i>Bon s.n.</i> (G); Hanoi: Nam Cong, 18 Nov. 1891, <i>Bon 4923</i> (P-4 sheets); Lao Cai: route de Lao Kay à Chapa, 200–1400 m, 25 Sept. 1943, <i>Petelot B. 390</i> (P-2 sheets) & entre Bao Nhai et Pakha, 500–600 m, 10 Dec. 1935, <i>Poilane 25021</i> (P-3 sheets); Yen Bai: Bao Ha, 21 Feb. 1936, <i>Poilane 25248</i> (BKF, P); Hoa Binh: Cho Bo, 15 Nov. 1887, <i>Balansa 2194</i> (P); Nghe An: Pu Mat, Khe Bu, 17 July 1998, <i>Khoi C 556</i> (HNU) & Pu Mat, Khe Bu, 17 July 1998, <i>Khoi C 557</i> (HNU); Ba Ria-Vung Tau: Long Son, Quan Ho, 20 Oct. 1911, <i>Lecomte & Finet 11</i> (P).</p>Published as part of <i>Saisorn, Witsanu & Chantaranothai, Pranom, 2022, A taxonomic revision of two genera, Pleurolobus and Sohmaea (Leguminosae) in Thailand and Indo-China, pp. 231-246 in Phytotaxa 573 (2)</i> on pages 237-238, DOI: 10.11646/phytotaxa.573.2.4, <a href="http://zenodo.org/record/7349951">http://zenodo.org/record/7349951</a>
Sohmaea H. Ohashi & K. Ohashi 2018
No full text2. Sohmaea H.Ohashi & K.Ohashi (2018b: 159). Type: Sohmaea laxiflora (DC. 1825a: 100) H.Ohashi & K.Ohashi (2018b: 162). Uraria subgen. Desmodiastrum Schindler (1925: 15). Type: Uraria henryi Schindl. (1925: 15). Desmodium subgen. Desmodium sect. Angustistipulosa H. Ohashi (1973: 97). Type: Desmodium laxiflorum DC. (1825a: 100). Herbs to shrubs. Leaves uni- or trifoliolate, petiolate, stipulate; leaflet coriaceous, petiolulate, stipellate, lateral veins reaching the margin. Inflorescences pseudoracemose, simple or occasionally paniculate, terminal or axillary; primary bract 1, caducous; secondary bract 1, caducous. Flowers papilionaceous, pedicellate; bracteole 1 or absent; calyx connate with 4 teeth; corolla 5, with 1 standard, 2 wings and 2 connate keels; stamens 10, diadelphous; ovary unicarpellate. Pods leguminous, with a terete, oblong article; seeds rim-arillate. Seven species distribute in Africa (Senegal and Burkina Faso), India eastward toward China, Myanmar through mainland southeast Asia, and Malesia. Five species are indigenous to Thailand, Laos, Cambodia, and Vietnam. Key to the species 1. Primary bracts bearing 2-fascicled flowers. Immature pods plicate............................................................................... 2. S. hispida 1. Primary bracts bearing 3–5-fascicled flowers. Immature pods straight 2. The length of terminal leaflets 2.2–3.6 times longer than width 3. Petioles less than 1 cm long. Pod articles less than 0.7 cm long....................................................................4. S. teres 3. Petioles more than 1 cm long. Pod articles more than 0.7 cm long............................................................5. S. zonata 2. The length of terminal leaflets less than 2 times of width 4. Flowers ca. 5 mm long. Pod articles 4–6 mm long...................................................................................1. S. diffusa 4. Flowers 4–4.5 mm long. Pod articles 3–4.5 mm long............................................................................ 3. S. laxifloraPublished as part of Saisorn, Witsanu & Chantaranothai, Pranom, 2022, A taxonomic revision of two genera, Pleurolobus and Sohmaea (Leguminosae) in Thailand and Indo-China, pp. 231-246 in Phytotaxa 573 (2) on pages 236-237, DOI: 10.11646/phytotaxa.573.2.4, http://zenodo.org/record/734995
Monopole-vortex complex in a theta vacuum
No full textWe discuss aspects of the monopole-vortex complex soliton arising in a
hierarchically broken gauge system, G to H to 1, in a theta vacuum of the
underlying G theory. Here we focus our attention mainly on the simplest such
system with G=SU(2) and H=U(1). A consistent picture of the effect of the theta
parameter is found both in a macroscopic, dual picture and in a microscopic
description of the monopole-vortex complex soliton
Vortices which do not Abelianize dynamically: Semi-classical origin of non-Abelian monopoles
No full textTalk given at the Fine Theoretical Physics Institute (FTPI) workshop, Continuous Advances in QCD (CAQCD-08), held May 15-18, 2008.Konishi, K.; Ohashi, Keisuke; Dorigoni, Daniele. (2008). Vortices which do not Abelianize dynamically: Semi-classical origin of non-Abelian monopoles. Retrieved from the University Digital Conservancy, https://hdl.handle.net/11299/42199
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