1,566 research outputs found
Osmylus (Osmylus) hyalinatus McLachlan 1875
No full text<i>Osmylus</i> (<i>Osmylus</i>) <i>hyalinatus</i> McLachlan, 1875 <p>(Figs 15, 18–19, 24, 27, 30–31, 36, 39–40)</p> <p> <i>Osmylus hyalinatus</i> McLachlan, 1875, 181.</p> <p>Other synonyms see Sekimoto & Yoshizawa (2011).</p> <p> <b>Description of 3rd instar larva.</b> BL 10.8–18.0 (13.3, n = 16) mm.</p> <p>Coloration. Head light brown, except for black colored stemmata and its surrounding parts; legs light yellow; dorsal side of thorax and abdomen basically light gray to gray; surrounding parts of DPa2 and DPm2 on meso- and metathoraces light brown; ventral side of thorax light yellow; surrounding parts of tubercles from metathorax to 8th abdominal segment yellow; sclerites brown; 9th and 10th abdominal segments and its sclerites light brown, subhyaline.</p> <p>Head (Fig. 15). Mandiblomaxillary stylets rather short, about 2.0 times as long as head capsule length; ML/ CW 2.3–2.4 (2.3, n = 16). Frontal edge of cranium with 15–20 short setae (n = 6), without pores. Antennae 39 or 40 segmented (n = 2).</p> <p>Prothorax (Fig. 18): DPc trapezoidal, separated with DM, its setae in middle part long, 1st to 3rd setae from within in posterior margin long. Mesothorax (Figs 18–19): DPm1 present; two short seta bearing on DPm2; DPm2 somewhat wide, its seta on anterior margin long; a seta on DPp1and DPp2 long. Metathorax (Figs 18–19): DAa expanded; DAm2 and DAm3 separated.</p> <p>First abdominal segment (Fig. 24): DM1 absent; DM2, DPp1, and DPp4 roughly the size of DPp2; a seta on DM2, DPp1, and DPp4 long; DPa present; a seta in dorso-anterior part of LP long. Second to 5th abdominal segment (Fig. 24): DM3 absent; a seta on LA long. Sixth abdominal segment (Fig. 24): VM3 absent; other character states same to 2nd to 5th abdominal segments. Seventh abdominal segment (Fig. 27): VM3 absent. Eighth abdominal segment (Fig. 24): DPp1+DPp2 with a pore on anterior margin. Ninth abdominal segment (Figs 30–31): Dc bearing 7 pairs of long setae in posterior half margin; outer setal row on VPc composed of 2 setae and a pore in exterior margin.</p> <p> <b>Material examined.</b> 2 exs., Takao-san, Takao-machi, Hachiôji-shi, Tokyo, 23.ii.2011 (collected in 3IL), 2.iv.2011 / 26.iii.2011 (PP), 15.iv.2011 / 7.iv.2011 (EM), S. Matsuno leg.; 2exs., Morito-gawa, Hayama-machi, Miura-gun, Kanagawa Pref., 24.ii.2011 (collected in 3IL), 15.iv.2011 / 15.iv.2011 (PP), 26.iv.2011 / 27.iv.2011 (EM), S. Matsuno leg.; 1 ex., (3IL), Kunigami, Bunsui-cho, Niigata Pref., 13.iii.2007, M. Hayashi leg.; 2 exs., (2 3IL), Shinjô, Daitô-cho, Unnan-shi, Shimane Pref., 8.viii.2007, M. Hayashi leg.; 2 exs., Hijiri-ko campsite, Kitahiroshima-chô, Yamagata-gun, Hiroshima Pref., 30.iv.2011 (collected in 3IL), 15.v.2011 / 17.v.2011 (PP), 24.v.2011 / 26.v.2011 (EM), S. Matsuno leg.; 5 exs. (1 2IL & 4 3IL), Kanmuri-kôgen, Yoshiwa, Hatsukaichi-shi, Hiroshima Pref., 25.ix.2010, M. Sakamoto leg.; 1 ex., Saragamine, Tôon-shi, Ehime Pref., 12.vi.2009 (collected in 3IL), 7.vii.2009 (PP), 21.vii.2009 (EM), R. Ogawa leg.; 1 ex. (3IL), same locality, 6.iii.2009, H. Yoshitomi leg.; 2 exs. (3IL), same locality, 26.iii.2009, S. Matsuno leg.; 7 exs. (5 1IL & 2 3IL), same locality, 11.x.2010, S. Matsuno leg.; 1 ex. (3IL), same locality, 26.x.2010, S. Matsuno leg.; 1 ex. (2IL), Omogokei, Kumakôgen-chô, Ehime Pref., 19.viii.2010, S. Matsuno leg.; 3 exs. (2IL), same locality and collector, 14.ix.2010; 2 exs. (3IL), same locality and collector, 23.xi.2010; 1ex., Omogo-kei, same locality, 7.iii.2011 (collected in 3IL), 8.iv.2011 (PP), 21.iv.2011 (EM), S. Matsuno leg.; 3 exs. (1 2IL & 2 3IL), same locality, 13.xi.2011, S. Matsuno leg.; 2 exs., Komeno-machi, Matsuyama-shi, Ehime Pref., 12.iv.2009 (collected in 3IL), 20.iv.2009 / 21.iv.2009 (PP), 30.iv.2009 / 1.v.2009 (EM), S. Matsuno leg.; 3 exs. (3IL), Sugesawa-machi, Matsuyama-shi, Ehime Pref., 7.xii.2011, S. Matsuno leg. 3 exs. (2IL), Higashino, Matsuyama-shi, Ehime Pref., 3.xi.2011, S. Matsuno leg.</p> <p> <b>Remarks.</b> This species is similar to the sympatric species, <i>O.</i> (<i>O.</i>) <i>pryeri</i>, in general appearance (e.g., coloration of body), but clearly differs from it in the shorter mandiblomaxillary stylets (Fig. 36).</p> <p> <b>Biological notes.</b> This is the most common species in Japan, and collected from ca. 100–1,000 m in altitude. They frequently hide in pockets under waterlogged decayed wood lying in small and shallow streams (Figs 39–40). In some cases, they were collected from under stones or in moss in a stream.</p> <p>The pupal periods are 10–12 days (10.7 days in average) in a rearing condition of under 22? (n = 3), 9 days under 20? (n = 2), and 11–13 days (12.2 days in average) under 18? (n = 5).</p> <p> <b>Distribution.</b> Japan (Hokkaidô, Rishiri, Kunashir, Honshû, Shikoku, Kyûshû, Yakushima).</p>Published as part of <i>Matsuno, Shigetomi & Yoshitomi, Hiroyuki, 2016, Descriptions of three larvae of Osmylus species from Japan (Neuroptera: Osmylidae), with a proposed naming system for the larval sclerites, pp. 348-366 in Zootaxa 4189 (2)</i> on pages 356-358, DOI: 10.11646/zootaxa.4189.2.9, <a href="http://zenodo.org/record/165942">http://zenodo.org/record/165942</a>
Periprosthetic acetabular bone loss using a constrained acetabular component
No full textThis is the author-created version of Springer, Ito, Hiroshi ; Matsuno, Takeo,Archives of Orthopaedic and Trauma Surgery, 124(2), 2004, 137-139. The original publication is available at www.springerlink.com.
authorWe describe two patients with a constrained acetabular component who required treatment for recurrent dislocation showing postoperative periprosthetic acetabular bone loss. These hips required revision surgery and demonstrated considerable bone loss caused by the migrated acetabular component. Impingement may have occurred with increased stress at the bone-prosthesis interface, and the sharp ends of screws with a metal shell may have gradually plowed up the acetabular bone. These failures illustrate the potential risk of using a constrained acetabular component
Discrimination of wine using taste and smell sensors
No full textThe taste-smell sensory fusion was conducted by combining a taste sensor array using lipid/polymer membranes and a smell sensor array using conducting polymer elements. Responses to different brands of wine were investigated and a clear discrimination among different samples was obtained by processing the data from either type of sensors. The effect of the aging process on the quality of wine was also studied. It was found that the system can discriminate among differently aged samples of the same red wine. The information provided by one type of array is independent of that provided by the other and their combination enhances the overall information available concerning the sample being measured. This suggests that the sensory fusion can be a powerful way to improve the performance of sensor technologies currently available
International Consensus Guidelines for Management of Intraductal Papillary Mucinous Neoplasms and Mucinous Cystic Neoplasms of the Pancreas.
No full textTriatoma matsunoi Fernandez-Loayza
No full textSpecies. T. matsunoi Fernández-Loayza Synonym of Hermalentia matsunoi (Fernández-Loayza) Etymology. The species name matsunoi has been assigned to honor Dr. Alejandro Yoshio Matsuno Matsuno (May 14, 1931, to January 2, 1982), a physician and epidemiologist within the Ministry of Health’s Malaria Eradication and Chagas Disease Control Program (PEMCC), because of his selfless work and the teachings given to this author (Fernández-Loayza 1989: 24). Original citation. “Se há asignado el nombre específico matsunoi en honor al Dr. Alejandro Yoshio Matsuno Matsuno (14.V. 31 - 2 I. 82) médico epidemiólogo del Programa de Erradicación de la Malaria Y Control de Chagas (PEMCC) del Ministério de Salud por su abnegada labor y lãs enseñanzas brindadas al autor” (Fernández-Loayza 1989: 24).Published as part of Gonçalves, Teresa Cristina Monte, Novo, Shênia Patrícia Corrêa, Lopes, Catarina Macedo & Santos-Mallet, Jacenir Reis Dos, 2009, Etymology of Triatomine Species (Hemiptera: Reduviidae: Triatominae), pp. 1-26 in Zootaxa 2148 on page 17, DOI: 10.5281/zenodo.18869
Improved mixing time for k-subgraph sampling*
No full text| openaire: EC/H2020/654024/EU//SoBigDataUnderstanding the local structure of a graph provides valuable insights about the underlying phenomena from which the graph has originated. Sampling and examining k-subgraphs is a widely used approach to understand the local structure of a graph. In this paper, we study the problem of sampling uniformly k-subgraphs from a given graph. We analyse a few different Markov chain Monte Carlo (MCMC) approaches, and obtain analytical results on their mixing times, which improve significantly the state of the art. In particular, we improve the bound on the mixing times of the standard MCMC approach, and the state-of-the-art MCMC sampling method PSRW, using the canonical-paths argument. In addition, we propose a novel sampling method, which we call recursive subgraph sampling RSS, and its optimized variant RSS+. The proposed methods, RSS and RSS+, are provably faster than the existing approaches. We conduct experiments and verify the uniformity of samples and the efficiency of RSS and RSS+.Peer reviewe
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