103,399 research outputs found
Brief von Toshio Ogata an Josef Steindl
No full textBRIEF VON TOSHIO OGATA AN JOSEF STEINDL
Brief von Toshio Ogata an Josef Steindl ([1])
Letter ([1])
Risk, staganation and control in modern capitlism (provisional): The selected essays of Josef Steindl. Ed. by. A. S. Eichner & T. Ogata. ([2])
Envelope (-
Crematogaster vieti Hosoishi & Ogata 2016, SP. NOV.
No full textCREMATOGASTER VIETI SP. NOV. (FIGS 122, 123) Holotype worker. Y Linh Ho, Sa Pa, Lao Cai, VIETNAM, Small fragment of forest (c. 1100 m alt.), 1.v.2002 (Eg 02- VN-225) (K. Eguchi) (IEBR). Paratypes. Two workers, same data as holotype (ACEG, KUEC); three workers, Y Linh Ho, Sa Pa, Lao Cai, VIETNAM, Small fragment of forest (c. 1100 m alt.), 1.v.2002 (Eg 02-VN-215) (K. Eguchi) (BMNH, CASC, THNHM). Worker measurements ( n = 9): HW 0.42–0.70; HL 0.45– 0.64; CI 92–113; SL 0.37–0.51; SI 72–88; EL 0.10– 0.16; PW 0.26–0.39; WL 0.54–0.75; PSL 0.07–0.14; PtL 0.17–0.24; PtW 0.13–0.20; PtH 0.12–0.18; PpL 0.11– 0.16; PpW 0.15–0.21; PtHI 74–86; PtWI 77–88; PpWI 120–154; WI 95–111. General description of woker: Workers weakly polymorphic in size. Head subquadratic in full-face view. Mandibles with four teeth arranged at an equal distance, apical and subapical teeth large, basal two teeth smaller. Anterior clypeal margin weakly convex in medial portion. Compound eyes distinctly projecting beyond lateral margins of head in full-face view. Scapes reaching posterolateral corners of head. Pronotal collar with almost straight anterior margin in dorsal view, distinctly lower than pronotum in lateral view. Pronotal dorsum with distinct ridges laterally. Mesonotal dorsum with lateral ridges that irregularly extend posteriad to tips of propodeal spines. Pronotum and mesonotum in lateral view not clearly forming continuous dorsal outline. Metanotal groove in dorsal view transverse, almost straight in median portion, forming deep concavity that is laterally margined by lamellate ridges. Propodeal spiracles oval, situated at posterolateral corners of propodeum, apart from or touching metapleural gland bullae. Propodeal spines developed, longer than diameter of propodeal spiracles, in dorsal view directed posteriad. Petiole in dorsal view with parallel sides and angulate shoulders anteriorly, longer than wide. Posterior portion of petiole with short process that is slightly higher than posterior margin of petiole disc in lateral view. Subpetiolar process developed as acute process. Postpetiole in lateral view with weakly convex dorsum, as high as petiole, in dorsal view as wide as petiole, globular, not bilobed. Subpostpetiolar process developed as acute process. Integument essentially smooth and shining. Dorsal surface of head generally smooth and shining, but weakly with rugulae on surrounding region of antennal sockets. Mandibles with feeble rugulae and smooth interspaces. Clypeus generally smooth and shining, but with two distinct pairs of longitudinal rugulae; rugulae not extending to posterior clypeal margin. Anterolateral shoulders of pronotum with rugulae. Dorsal surface of pronotum with longitudinal rugulae. Lateral surface of pronotum smooth and shining. Mesopleura weakly sculptured, but relatively smooth on central areas. Rugula on higher portion of mesopleura extending to small pit of mesothoracic spiracles. Dorsal surface of propodeum with rugulae. Dorsal surface of petiole smooth and shining. Lateral surface of petiole weakly sculptured. Dorsal and lateral surfaces of postpetiole smooth and shining. Standing pilosity sparse. Dorsal face of head with two to three pairs of erect and stout long setae, and short and decumbent setae sparsely. Clypeus with two pairs of long setae in anterior portion, one directed upward and the other downward. Anterior clypeal margin with one pair of long setae medially and some pairs of short setae laterally. Scapes with suberect to decumbent setae. Mesosoma with four pairs of long erect and stout setae (ps1PN, psaMN, pspMN, and ps1PS) that are much longer than other erect setae. Posterolateral tubercles of petiole posteriorly with one pair of stout long setae. Postpetiole with four pairs of stout long setae on disc anterodorsally, anterolaterally and posteriorly. Fourth abdominal tergite with erect and stout setae sparsely, and short decumbent setae sparsely. Body yellow. All flagellar segments yellow. Intermediate worker measurements ( n = 1): HW 0.68; HL 0.70; CI 97; SL 0.54; SI 79; EL 0.19; PW 0.47; WL 0.95; PSL 0.19; PtL 0.32; PtW 0.25; PtH 0.24; PpL 0.20; PpW 0.28; PtHI 75; PtWI 78; PpWI 140; WI 112. Description of intermediate worker: With worker character conditions, except as follows. Vestigial lateral ocelli present. Mesonotum highly convex in lateral view. Mesonotal dorsum without lateral ridges. Pronotum not clearly forming same dorsal outline with mesonotum in lateral view, but posterior face forming oblique slope to metanotal groove. Propodeal spiracles touching metapleural gland bulla. Petiole wth subparallel sides in dorsal view, tapering anteriorly. Subpetiolar process developed as blunt process. Dorsal surface of pronotum smooth and shining. Dorsal surface of mesonotum with rugulae anteriorly and laterally. Mesopleura generally smooth, but oblique sulcus running from anterior areas. Anterodorsal surface of propodeum with rugulae reticulately. Anterior clypeal margin with one single and one pair of long setae on median portion and some pairs of short setae laterally. Mesosoma with several pairs of long setae on promesonotum, one ps1PS. Posterolateral tubercles of petiole with two to three pairs of stout long setae posteriorly. Fourth abdominal tergite with suberect to decumbent setae abundantly. Comments: In the worker this species can be distinguished from all other members of the C. biroi group by the distinct compound eyes, generally smooth dorsal surface of head, petiole with subparallel sides in dorsal view, and erect setae on body tapering distally. This species is very similar to C. osakensis, but distinguished from it by the thick propodeal spines and petiole with subparallel sides. This species corresponds to sp. 36 of SKY (Eguchi et al., 2005) and sp. eg-1, sp. eg-4 by Eguchi et al. (2011). Distribution: This species is known from Vietnam (Fig. 51). Etymology: The species name is dedicated to Dr. Bui T. Viet, who helped with field surveys in Vietnam. Material examined: VIETNAM: one worker, Tam Dao 1000 m alt., Vinh Phuc Prov., N. Vietnam, 8.viii.1998 (Sk. Yamane); one worker, Tam Dao 1000 m alt., Vinh Phuc Prov., N. Vietnam, 9.viii.1998 (Sk. Yamane); two workers, Tam Dao 1000 m alt., Tam Duong Dist., Vinh Prov., 6.xi.2001 (K. Ogata); four workers, Ba Vi 460 m alt., Ba Vi Dist., Ha Tay Prov., 11.xi.2001 (K. Ogata); two workers, Ba Vi 670 m alt., Ba Vi Dist., Ha Tay Prov., 12.xi.2001 (K. Ogata); four workers, Tu Lung, Mai Chau Dist., Hoa Binh Prov., 27.xi.1999 (K. Ogata); three workers, Small fragment of forest (c. 1100 m alt.), Y Linh Ho, Sa Pa, Lao Cai, 1.v.2002 (Eg 02-VN-215) (K. Eguchi); three workers, Small fragment of forest (c. 1100 m alt.), Y Linh Ho, Sa Pa, Lao Cai, 1.v.2002 (Eg 02-VN-225) (K. Eguchi); four workers, M. Nghe An, Pu Hoat, Lung Khung (640 m alt.), 5.xi.1999 (code- 011) (T. V. Bui); one worker, Chua Yen Tu (720– 845 m alt.), Quang Ninh, 19.v.2004 (K. Eguchi); two workers and one intermediate worker, near Forestry Station (253 m alt.), Khe Kem, Pu Mat N. P., Nghe An, 15.iii.2006 (Eg 15iii06-03) (K. Eguchi). Species excluded from the subgenus Orthocrema in Asia.Published as part of Hosoishi, Shingo & Ogata, Kazuo, 2016, Systematics and biogeography of the ant genus Crematogaster Lund subgenus Orthocrema Santschi in Asia (Hymenoptera: Formicidae), pp. 547-606 in Zoological Journal of the Linnean Society 176 (3) on pages 601-602, DOI: 10.1111/zoj.12330, http://zenodo.org/record/535818
Data for: Formal Analysis of a Security Protocol for e-Passports based on Rewrite Theory Specifications
No full textnpw.maude --- Maude specification of the naive login protocol, including model checking codeotpw.maude --- Maude specification of the one-time login protocol, including model cgecking codepace6-1.maude --- Maude speicification of the original PACE protocol, inclusindg model cgecking code for T-Corrpace6-2.maude --- Maude speicification of the original PACE protocol, inclusindg model cgecking code for C-Corrrevpace0-1.maude --- Maude speicification of the revised PACE protocol, inclusindg model cgecking code for T-Corrrevpace1-1.maude --- Maude speicification of the revised PACE protocol, inclusindg model cgecking code for C-Cor
Probolomyrmex okinawensis Terayama et Ogata
No full textProbolomyrmex okinawensis Terayama et Ogata (Figs. 6A-F, 9F, 10F) Probolomyrmex okinawensis Terayama et Ogata, 1988: 591-592, figs. 1-5. Holotype: worker, Chibana, Okinawa-hontou Is. [Okinawa-jima], Ryukyus, Japan, 19/iii/1983, T. Mizutani (Faculty of Agriculture, Kyushu Univ., Japan) [examined].Paratypes: 4 workers from the same nest as the holotype [one paratype examined (loaned from the Institute of Tropical Agriculture, Kyushu Univ.)];1 dealate queen and 1 worker, Nakasone, Okinawa-hontou Is., 20/xi/1975, T. Abe [not examined];1 dealate queen from Nakijin-joushi, Okinawa-hontou Is., 7/iii/1984, K. Onoyama [examined (loaned from the Institute of Tropical Agriculture, Kyushu Univ.)]. Recognition. This species is similar to P. maryatiae sp. nov. and P. vieti sp. nov., but distinguished from the latter two by the posteroventral portion of subpetiolar process forming only an obtuse angle in the worker and queen. Distribution. Known only from Okinawa-jima (C. Ryukyus).Published as part of Eguchi, K., Yoshimura, M. & Yamane, S., 2006, The Oriental species of the ant genus Probolomyrmex (Insecta: Hymenoptera: Formicidae: Proceratiinae)., pp. 1-35 in Zootaxa 1376 on page 2
Kagami-Ogata syndrome in a patient with 46,XX,t(2;14)(q11.2;q32.2)mat disrupting MEG3
No full textKagami-Ogata syndrome (KOS14) is a rare imprinting disorder characterized by a unique constellation of phenotypes including bell-shaped small thorax with coat-hanger appearance of the ribs. We encountered an African American female infant with KOS14 phenotype and 46,XX,t(2;14)(q11.2;q32.2)mat. After excluding upd(14)pat and an epimutation (hypermethylation) and a deletion affecting the maternally derived 14q32.2 imprinted region, we performed whole-genome sequencing, revealing that the translocation was generated between noncoding region at 2q11.2 and intron 6 of MEG3 at 14q32.2. Subsequent Sanger sequencing for the fusion points showed that the chromosomal fusion on the der(2) chromosome occurred between Chr2:102,193,994 (bp) and Chr14:101,314,628 (bp) in association with an insertion of 5-bp segment of unknown origin and that on the der(14) chromosome took place between Chr14:101,314,627 (bp) and Chr2:102,193,995 (bp) in association with an insertion of 1-bp segment of unknown origin (according to GRCh37/hg19). The results, together with the previous data in patients with KOS14, imply that the MEG3 disruption by 46,XX,t(2;14)(q11.2;q32.2)mat caused silencing of all MEGs including RTL1as and resultant excessive RTL1 expression, leading to the development of KOS14. To our knowledge, while Robertsonian translocations involving chromosome 14 have been reported in KOS14, this is the first case of KOS14 caused by a chromosomal translocation involving the 14q32.2 imprinted region
Phase diagram of the 1-dimensional t--J mode
No full textThe phase diagram of the one-dimensional t-J model is investigated by analyzing the results of exact diagonalization and the exact solutions at J/t=0 and 2. Phase separation takes place above a critical value of J around Jc/t=2.5 3.5 depending on the electron density. In the small-J region, Tomonaga-Luttinger liquid theory holds and its correlation exponents are calculated as a function of J/t and the electron density. Superconducting correlations become dominant in a region between the solvable case (J/t=2) and phase separation. A spin-gap region is also found at low density. © 1991 The American Physical Society
Letter, [Author unclear] to Paulina T. Merritt
No full textHandwritten letter to Paulina Merritt from an unknown author, October 1, 1876.
Gravestone for Toshiro Ogata, "Manzanar, a photograph essay: Manzanar today"
No full textA photograph of gravestone in cemetery. Engraved name reads: Ogata Toshiro, Baby Jerry Ogata. The caption reads, "Some would remain forever. Manzanar. Chris Uyemura Collection." A page from: Manzanar, a photograph essay (csudh_uye_0001).The Chris S. Uyemura Manzanar Photograph Collection consists of a pictorial essay, “Manzanar, a photographic essay,” and additional loose photos, which were compiled and collected by Chris S. Uyemura. The essay contains photographs, texts, and newspaper clippings, and was submitted to Professor Donald T. Hata of the Department of History at CSU Dominguez Hills. The collection depicts the incarceration of people of Japanese ancestry in the Manzanar camp during World War II as well as reflects the events, contrasting with photographs of the Manznar National Historic Site, which illustrates what is left of the camp today. The collection was originally named as “Asian Pacific Studies Collection Box 14.
Phylogenetic analyses of severe acute respiratory syndrome coronavirus 2 reveals multiple routes of introduction into Taiwan, the United States, Japan, and other countries
No full textSupplemental Table 1. Genome sequences used in this study.
Supplemental Figure 1. Variable sites found from SARS-CoV-2 ORF sequences
After alignment, the SARS-CoV-2 sequences had 112 variable sites from 29,148 bps aligned ORF sequences from 76 samples isolated from humans. Dots indicate the identical bases with the reference bases on the top of the alignment. A, C, G or T indicate the differences in the sequences. Nucleotide position numbers in the reference genome are shown above the alignment. All sites containing gaps were removed from the analysis.
Supplemental Figure 2. Topological phylogeny of SARS-CoV-2
Maximum-likelihood phylogenetic analyses under each condition below. Blue, green, and yellow branches indicate group TCT, TCC, and CTC respectively. Bootstrap values (≧30%) based on 1,000 replications are indicated at nodes. Branch length was meaningless. (A) No separate condition. Final log-likelihood was −59284.685031. BIC score was 120234.752998. (B) Separating 1st/2nd and 3rd codon position condition. Final log-likelihood was − 56877.337100. BIC score was 115522.858552. (C) Separating each ORF condition. Final log-likelihood was −59849.040154. BIC score was 121764.388766. (D) Separating each ORF and also 1st/2nd and 3rd codon position condition. Final log-likelihood was − 56521.449588. BIC score was 115530.693437. (E) Separating each ORF and each codon position condition. Final log-likelihood was −56149.612346. BIC score was 115074.862919.
Supplemental File 1. Parsimony informative sites found in SARS-CoV genomes.
Supplemental File 2. Parsimony informative sites found in Ebola virus genomes.
Supplemental File 3. Parsimony informative sites found in Zika virus genomes
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