566 research outputs found
lcfiplus/LCFIPlus: v00-10-01
No full textv00-10-01
2021-11-19 YONAMINE Ryo (PR#61)
add dummy primary-vertex to avoid accessing null pointer unless actual one is found.
2020-12-09 Tomohiko Tanabe (PR#54)
Fix typos in reading input values for the FlavorTag algorithm related to the number of VTX hits used for computing joint probabilitie
FIGURE. 2 in Reassessment of species delimitation using nuclear markers in three lentic-breeding salamanders from the Chugoku District of Japan (Amphibia: Caudata: Hynobiidae)
No full textFIGURE. 2. Bayesian tree based on the complete cyt-b gene for the Hynobius akiensis sensu lato and related species. Asterisks above branches indicate nodes with bootstrap supports for ML inference (bs)>70 % and Bayesian posterior probability (bpp)>95 %.Published as part of Tomimori, Yusuke, Matsui, Masafumi, Okawa, Hiroshi, Nishikawa, Kanto, Tanabe, Shingo & Kamasaka, Ryo, 2023, Reassessment of species delimitation using nuclear markers in three lentic-breeding salamanders from the Chugoku District of Japan (Amphibia: Caudata: Hynobiidae), pp. 145-160 in Zootaxa 5293 (1) on page 151, DOI: 10.11646/zootaxa.5293.1.6, http://zenodo.org/record/795983
山村での生活が子どものメラトニン反応に及ぼす影響
No full text掲載誌：Shingo Noi, Akiko Shikano, Naoko Yamada, Ryo Tanaka, Kosuke Tanabe and Hideyuki Tsuji (2021). Effects of change in residence to a mountain village on children’s melatonin responses, Biological Rhythm Research, 52(1): 60–69.研究紹介 : 国外学術誌掲載論文か
Effects of change in residence to a mountain village on children’s melatonin responses
No full text掲載誌：Shingo Noi, Akiko Shikano, Naoko Yamada, Ryo Tanaka, Kosuke Tanabe and Hideyuki Tsuji (2021). Effects of change in residence to a mountain village on children’s melatonin responses, Biological Rhythm Research, 52(1): 60–69.研究紹介 : 国外学術誌掲載論文からdepartmental bulletin pape
Measuring the top Yukawa coupling at the ILC at = 500 GeV
No full textWe report on the feasibility of the direct measurement of the top Yukawa coupling g_t at the International Linear Collider (ILC) during its first phase of operation with a center-of-mass energy of 500 GeV. The signal and background models incorporate the non-relativistic QCD corrections which enhance the production cross section near the t-tbar threshold. The e+e- -> t tbar H signal is reconstructed in the 6-jet + lepton and the 8-jet modes. The results from the two channels are combined. The background processes considered are e+e- -> t bbar W- / tbar b W+ (which includes e+e- -> t tbar), e+e- -> t tbar Z, and e+e- -> t tbar g* -> t tbar b bar. We use a realistic fast Monte-Carlo detector simulation. Signal events are selected using event shape variables, through jet clustering, and by identifying heavy flavor jets. Assuming a Higgs mass of 120 GeV, polarized electron and positron beams with (Pe-,Pe+) = (-0.8,+0.3), and an integrated luminosity of 1 ab-1, we estimate that the e+e- -> t tbar H events can be seen with a statistical significance of 5.2 sigma, corresponding to the relative top Yukawa coupling measurement accuracy of |Delta g_t / g_t| = 10%.We report on the feasibility of the direct measurement of the top Yukawa coupling g_t at the International Linear Collider (ILC) during its first phase of operation with a center-of-mass energy of 500 GeV. The signal and background models incorporate the non-relativistic QCD corrections which enhance the production cross section near the t-tbar threshold. The e+e- -> t tbar H signal is reconstructed in the 6-jet + lepton and the 8-jet modes. The results from the two channels are combined. The background processes considered are e+e- -> t bbar W- / tbar b W+ (which includes e+e- -> t tbar), e+e- -> t tbar Z, and e+e- -> t tbar g* -> t tbar b bar. We use a realistic fast Monte-Carlo detector simulation. Signal events are selected using event shape variables, through jet clustering, and by identifying heavy flavor jets. Assuming a Higgs mass of 120 GeV, polarized electron and positron beams with (Pe-,Pe+) = (-0.8,+0.3), and an integrated luminosity of 1 ab-1, we estimate that the e+e- -> t tbar H events can be seen with a statistical significance of 5.2 sigma, corresponding to the relative top Yukawa coupling measurement accuracy of |Delta g_t / g_t| = 10%
Rhopilema asamushi Uchida (Cnidaria, Scyphozoa, Rhizostomidae) newly occurred in Tanabe Bay, Wakayama Prefecture, Japan
No full textA blue jellyfish body fragment of Rhopilema asamushi Uchida, that is identifiable by mitochondrial gene analysis (COI gene sequences: 644 bps), is washed ashore at Hatakejima Island in Tanabe Bay, Wakayama Prefecture, Japan. This occurrence is the first record in the Pacific side of southern Japan
子どもと青年の睡眠習慣につながる経路 : 東京都世田谷区での悉皆調査
No full text掲載誌: Shingo Noi, Akiko Shikano, Ryo Tanaka, Kosuke Tanabe, Natsuko Enomoto, Tetsuhiro Kidokoro, Naoko Yamada and Mari Yoshinaga (2021). The pathways linking to sleep habits among children and adolescents: A complete survey at Setagaya-ku, Tokyo, International Journal of Environmental Research and Public Health, 18(12): 6309.
doi: https://doi.org/10.3390/ijerph18126309研究紹介 : 国外学術誌掲載論文か
The pathways linking to sleep habits among children and adolescents : a complete survey at Setagaya-ku, Tokyo
No full text掲載誌: Shingo Noi, Akiko Shikano, Ryo Tanaka, Kosuke Tanabe, Natsuko Enomoto, Tetsuhiro Kidokoro, Naoko Yamada and Mari Yoshinaga (2021). The pathways linking to sleep habits among children and adolescents: A complete survey at Setagaya-ku, Tokyo, International Journal of Environmental Research and Public Health, 18(12): 6309.
doi: https://doi.org/10.3390/ijerph18126309研究紹介 : 国外学術誌掲載論文からdepartmental bulletin pape
Ground Truth for DCASE 2021 Challenge Task 2 Evaluation Dataset
No full textDescription
This data is the ground truth for the "evaluation dataset" for the DCASE 2021 Challenge Task 2 "Unsupervised Anomalous Sound Detection for Machine Condition Monitoring under Domain Shifted Conditions".
In the task, three datasets have been released: "development dataset", "additional training dataset", and "evaluation dataset". The evaluation dataset was the last of the three released and includes around 200 samples for each machine type, section index, and domain, none of which have a condition label (i.e., normal or anomaly). This ground truth dataset contains the condition labels.
Data format
The CSV file for each machine type, section index, and domain includes the ground truth data like the following:
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section_03_source_test_0000.wav,1
section_03_source_test_0001.wav,1
...
section_03_source_test_0198.wav,0
section_03_source_test_0199.wav,1
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The first column shows the name of a wave file. The second column shows the condition label (i.e., 0: normal or 1: anomaly).
How to use
A script for calculating the AUC, pAUC, precision, recall, and F1 scores for the "evaluation dataset" is available on the Github repository [URL]. The ground truth data are used by this system. For more information, please see the Github repository.
Conditions of use
This dataset was created jointly by Hitachi, Ltd. and NTT Corporation and is available under a Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International (CC BY-NC-SA 4.0) license.
Publication
If you use this dataset, please cite all the following three papers:
Yohei Kawaguchi, Keisuke Imoto, Yuma Koizumi, Noboru Harada, Daisuke Niizumi, Kota Dohi, Ryo Tanabe, Harsh Purohit, and Takashi Endo, "Description and Discussion on DCASE 2021 Challenge Task 2: Unsupervised Anomalous Sound Detection for Machine Condition Monitoring under Domain Shifted Conditions," in arXiv e-prints: 2106.04492, 2021. [URL]
Noboru Harada, Daisuke Niizumi, Daiki Takeuchi, Yasunori Ohishi, Masahiro Yasuda, Shoichiro Saito, "ToyADMOS2: Another Dataset of Miniature-Machine Operating Sounds for Anomalous Sound Detection under Domain Shift Conditions," in arXiv e-prints: 2106.02369, 2021. [URL]
Ryo Tanabe, Harsh Purohit, Kota Dohi, Takashi Endo, Yuki Nikaido, Toshiki Nakamura, and Yohei Kawaguchi, "MIMII DUE: Sound Dataset for Malfunctioning Industrial Machine Investigation and Inspection with Domain Shifts due to Changes in Operational and Environmental Conditions," in arXiv e-prints: 2105.02702, 2021. [URL]
Feedback
If there is any problem, please contact us:
Yohei Kawaguchi, [email protected]
Daisuke Niizumi, [email protected]
Keisuke Imoto, [email protected]
Riukiaria mundyi Korsós, Nakamura & Tanabe, 2011, sp. n.
No full textRiukiaria mundyi sp. n. Figs 4 –6, 14– 19. Holotype male (NSMT-My 379)— Japan, Southern Ryukyus, Yaeyama Group, Yonaguni-jima Island, Mt. Dunandake, primary forest, N 24.4577 ° E 122.9711 °, 146 m alt., 31 August 2009, leg. Z. Korsós & Y. Nakamura. Paratypes: 3 males, 5 females, 2 juvs. (RUMF, HNHM)—Same locality and date. 1 male, 1 female (RUMF)— Japan, Southern Ryukyus, Yaeyama Group, Yonaguni-jima Island, Adigara Cave area, near construction place, N 24.4599 ° E 122.9594 °, 44 m alt., 2 September 2009, leg. Z. Korsós & Y. Nakamura 2 females (NSMT-My 380)— Japan, Southern Ryukyus, Yaeyama Group, Yonaguni-jima Island, Arakawabana forest trail, 134 m, primary forest, N 24.4441 ° E 123.0107 °, 1 September 2009, leg. Z. Korsós & Y. Nakamura 4 males, 5 females, 3 juvs. (RUMF, HNHM)— Japan, Southern Ryukyus, Yaeyama Group, Yonaguni-jima Island, Kubura-bari, N 24 ° 27.4 ’ E 122 ° 56.6 ’, 50 m alt., rocky grassland, 14 February 2010, leg. R. & Z. Korsós Diagnosis. A member of the genus Riukiaria as defined by Shinohara (1977) and Tanabe and Shinohara (1996) with the simple, forceps-like male gonopod conformation. It differs from congeners first of all by its coloration in life (almost uniformly pinkish-orange), by its exclusive occurrence on a single island (Yonaguni-jima), and in details of gonopod morphology. FIGURES 14–16. Riukiaria mundyi sp. n. 14 = Anterior body part paratype male, dorsal view; 15 = Epiproct of paratype male, dorsal view; 16 = Sternum, coxa, and prefemur of 2 nd legpair of paratype male, posterior view. Scales 1 mm (14,15) and 0.5 mm (16). Etymology. The specific epithet is a patronym in honor of Mr. Imre Mundy (Budapest), a Hungarian engineer, long time friend and supporter of the first author (genitive, masculine). Description. Measurements: Body size generally smaller than in most other Riukiaria species. Length of males 36–42 mm, midbody paranotal width 7.5–8 mm, metatergal length 1.8–2 mm, collum width 6–6.6 mm, length 2.4–3 mm (n= 4). Female body length 36–41 mm, midbody paranotal width 7.8–8.6 mm, metatergal length 1.8–2 mm, collum width 6.3–7.1 mm, length 2.8–3.3 mm (n= 8). Kubura-bari population (see Remarks): Male body length 25–26 mm, midbody paranotal width 5.1–5.3 mm, metatergal length 1.2–1.3 mm, collum width 4.4– 4.6 mm, length 1.9–2.1 mm (n= 4). Female body length 30–31 mm, midbody paranotal width 6.3–6.8 mm, metatergal length 1.3–1.4 mm, collum width 5.2–5.5 mm, length 2.5–2.6 mm (n= 5). Color in life (Fig. 4): Whole body is almost uniformly light orange, pinkish, occasionally tending toward reddish or dark yellowish. Head, prozona, legs, and underside paler, 6 th segment of antennae, tibiae and tarsi whitish. On collum and each metatergum a slightly darker, almost brownish median patch, pronounced towards paranota as oval spots. On preserved specimens (70 % ethanol) the vivid color quickly disappears, only shadows of the abovementioned pattern remains. Coloration of males and females does not differ. Fluorescence in UV light strong (Figs 5–6), especially on prozona and underside, metazona are slightly greyish. Head smooth, epicranial suture distinct, 2 + 2 frontal setae, several setae scattered above clypeus, with 2 dense rows at its margin and on labrum. Antennae straight, first article globose, 2 nd slightly clavate, subequal with articles 3 –5, 6th longest, about 1.2 x longer than 5 th, 7 th small, slender, slightly longer than wide. Gnathochilarial stipites and lamellae linguales covered densely with short hairs, large, triangular mentum with smaller, distinct, median hair-field. Collum convex, smooth, shiny, lateral and posterior margin with weak ridge, lateral corners triangular, slightly directed caudad. Pro- and metaterga smooth without any traces of tubercles or punctuation, not even wrinkles. Posteriolateral edge of paranota 2–3 triangular, on 4 th and onwards strongly pointed caudad (Fig. 14). Pore formula normal, pores on paranota 5,7,9,10,12,13,15,16, 17, and 18, in median excavation of paranota (in lateral view). Sides between segments 6–13 perfectly parallel, segments 14–19 gradually tapering, posteriolateral projections become more pointed. Epiproct in dorsal view subtriangular (Fig. 15), in lateral view protruding over paraprocts, parallel-sided, slightly curved ventrad, with 7 + 7 setae, 3 + 3 of them sitting on knobs. Paraprocts strongly marginate with 2 + 2 setae, hypoproct with 1 + 1 setae on knobs. Midbody legs well separated (by 1.8–1.9 mm in males, 2.4–2.8 mm in females), sterna wide and smooth. Postgonopodal legs with moderately developed ventral spine on prefemur, increasingly stronger towards body end, femur about twice as long as prefemur, straight, postfemur crassate, tibia straight, both subequal in length and about 1 / 3 rd of femur, tarsus slender, about twice as long as tibia, claw (ca. 0.5 mm long) curved. Sexual characters: Male 2 nd legpair (Fig. 16) coxa with strong median projections about half as long as length of coxa, apically with membraneous tubules surrounded by strong setae, 1 + 1 macrosetae sitting at joint of prefemur (1 anteriorly, and 1 posteriorly). No other sternal or leg modification could be observed. Male gonopodal aperture on segment 7 wide, elliptical, about twice as wide as long, gonopods in situ usually deeply embedded, with acropodites crossing each other. Coxa (Figs 17–18, c) long, slender, about twice as long as wide, without apophysis but with small apophyseal macroseta (cm). Cannula normal, hidden on mesal side. Telopodite consists of two simple processes (Figs 17–18) forming a simple, forceps-like appearance typical for Riukiaria (Tanabe & Shinohara 1996), the shorter branch being the prefemoral process (pfp), growing proximally from the base of prefemur, the latter being thick and short, and densely covered with long hairs. Prefemoral process about 3 / 4 th of length of acropodite, devoid of any seta, knob, or additional process, flattened, parallel-sided, spatula-shaped, almost transparent. Acropodite (as a continuation of prefemur) long, scythe-shaped, arched proximally towards prefemoral process, with its slightly broadened to triangular, pointed tip (s) almost bending back to that. Distinction between prefemur and acropodite indefinite, hairs becoming scarcier at about 1 / 3 rd of total length, but about half length still a strong macroseta (ms) on lateral side of acropodite. Prostatic groove runs straight medially along mesal side of acropodite, and ends indistinctly on its pointed tip. Female cyphopods (Fig. 19) closely packed behind 2 nd legpair, in large, ∞-shaped aperture, valves (v) are oval, nearly as high as wide, densely setose, operculum (op) on lateral side small, less than half as high as valves, with fewer and shorter but stronger setae, receptacles (r) embracing valves both anteriorly and posteriorly, subrectangular, with several series of short hairs only along ventral margin. Distribution. R. mundyi sp. n. is restricted to Yonaguni-jima Island, the southwesternmost member of the Yaeyama Island Group, southern Ryukyus, Okinawa Prefecture, Japan. Remarks. Yonaguni-jima island, the type locality of R. mundyi sp. n., is situated about 100 km east of Taiwan, and 80 km west of Iriomote-jima, another member of the Yaeyamas. On two of this latter island group, Iriomotejima and Ishigaki-jima islands, another species, R. chelifera, occurs. It is slightly larger (body length 45 mm), and its color pattern is different: head, antennae, proterga, large part of metaterga anteriorly dark brown or grey, posterior margin, paranota, tip of epiproct, and legs yellow. This is in strong contrast with the uniformly orange-yellow color of the new species. Male gonopods also differ, acropodite and prefemoral process being straight, slender, and almost equal in length, as opposed to the longer and curved acropodite with macroseta in R. mundyi sp. n. Comparison to the possible Taiwanese species, R. cohaesiva, R. contigua, and R. uraensis (from the region of Taipei, Wulai), all inadequately described and poorly illustrated by Wang (1956, 1957), is impossible without freshly collected material. Specimens of the new species in Yonaguni-jima were mostly collected along the edge of natural, deciduous forests, mostly in moist litter under the large leaves of Alocasia odora, but also close to human-disturbed areas like abandoned construction sites, ruined cave entrances etc. Adult specimens were collected at the locality Kuburabari, too, which is actually a pasture for the native, endemic race of horse (the Yonaguni pony), and these specimens were distinctly smaller than members of the other populations. This is perhaps due to that relatively harsh environment, the wind-swept rocky grassland on the western side of the island, generally poor in organic litter. The species was mentioned and illustrated as an undescribed Riukiaria from Yonaguni-jima island by Tanabe (2005). It was included into the Red Data Book of threatened wildlife of Okinawa and, though categorized as ’data deficient’ (DD), its habitat was proposed for preservation. According to our observations, the species is not confined to any characteristic or undisturbed biotope on Yonaguni-jima Island so perhaps habitat conservation is not the best approach, but considering that the total area of the island itself is only 28.8 square kilometers, the populations of the new and unique species are indeed worthy of legal protection.Published as part of Korsós, Zoltán, Nakamura, Yasuyuki & Tanabe, Tsutomu, 2011, Two new millipede species of the genus Riukiaria (Diplopoda, Polydesmida, Xystodesmidae) endemic to the Ryukyu Archipelago, Japan, pp. 55-68 in Zootaxa 2877 on pages 62-66, DOI: 10.5281/zenodo.27756
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