37,449 research outputs found

    Sphenanthias whiteheadi Talwar 1973

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    Sphenanthias whiteheadi Talwar, 1973 (Figs. 2–3) Diagnosis. Dorsal fin rays IV, 22–23; Anal fin rays 1, 16; Pectoral fin rays 19–20; Pelvic fin rays I, 5; Lateral Line scales 39–41. Gill rakers 18–21+ 35–39. Vertebrae 28. Pelvic fins long in males reaching on to anal, black pigmentation between membrane of maxilla and premaxilla (Talwar, 1973). Description. Measurements are given in Table.1. Values of type specimens in Talwar, 1973 follows in parenthesis. Body compressed, elongated with tapering tails. Males larger than females. Head large, head length 26.1–31.8 % SL (25.7–30 % SL) 3.1–3.8 in SL (3.3–3.9 in SL), body depth at dorsal origin 22.8–28.5% SL (25.1–30.9% SL), eyes large, eye length (bony orbit) 6.1–11.6 % SL (8–9.4% SL), interorbital 5.5–6.8% SL (6–6.9 % SL), mouth large, lower jaw projecting, maxilla broad. Lower margin of preopercle serrated with 6–9 spines. Opercle with small scales. Lateral line runs close to dorsal fin base and ends at dorsal fin last rays mostly at 22 nd and 23 rd rays. LL scales (pored) 36–38. Teeth in upper jaw uniserial, teeth absent in symphysis of both jaws. Pelvic fins in males elongate (Fig.2) 43–48% SL (43.3–55.6% SL) females (Fig.3) 24.7–30 % SL (28.8–35.7 % SL). Pelvic fin proximal ray attached to body. Dorsal fin base 64–68.5% SL. The first two dorsal fin spines placed closer than other spines. Caudal fin elongate and lanceolate. Sphenanthias whiteheadi cannot be mistaken with Sphenanthias simoterus Smith 1968. S. simoterus having peculiar characters; D III, 21; A I, 14; GR 13+ 24, LL 46–48 (Smith, 1968). DNA analysis. A 652 bp of mitochondrial COI region was amplified bidirectionaly for one specimen. Utilization. The species is primarily used for consumption. Common name. Indian bandfish Remarks. The specimens of Sphenanthias whiteheadi were collected off the coast of Tuticorin in the Gulf of Mannar at a depth of 220–350m by deep-sea shrimp trawler. The holotype and three paratypes were collected at Quilon, north of Tuticorin, along the southeast coast of India. This species may prove to be more widespread along the Indian coast. (n=8)Published as part of Bineesh, K. K., Sajeela, K. A., Akhilesh, K. V., Pillai, N. G. K. & Abdussamad, E. M., 2011, Redescription of Sphenanthias whiteheadi Talwar (Perciformes: Cepolidae) with DNA barcodes from the southern coasts of India, pp. 64-68 in Zootaxa 3098 (1) on pages 66-67, DOI: 10.11646/zootaxa.3098.1.7, http://zenodo.org/record/524527

    EPHA2 Polymorphisms and Age-Related Cataract in India

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    Objective: We investigated whether previously reported single nucleotide polymorphisms (SNPs) of EPHA2 in European studies are associated with cataract in India. Methods: We carried out a population-based genetic association study. We enumerated randomly sampled villages in two areas of north and south India to identify people aged 40 and over. Participants attended a clinical examination including lens photography and provided a blood sample for genotyping. Lens images were graded by the Lens Opacification Classification System (LOCS III). Cataract was defined as a LOCS III grade of nuclear >= 4, cortical >= 3, posterior sub-capsular (PSC) >= 2, or dense opacities or aphakia/pseudophakia in either eye. We genotyped SNPs rs3754334, rs7543472 and rs11260867 on genomic DNA extracted from peripheral blood leukocytes using TaqMan assays in an ABI 7900 real-time PCR. We used logistic regression with robust standard errors to examine the association between cataract and the EPHA2 SNPs, adjusting for age, sex and location. Results: 7418 participants had data on at least one of the SNPs investigated. Genotype frequencies of controls were in Hardy-Weinberg Equilibrium (p > 0.05). There was no association of rs3754334 with cataract or type of cataract. Minor allele homozygous genotypes of rs7543472 and rs11260867 compared to the major homozygote genotype were associated with cortical cataract, Odds ratio (OR) = 1.8, 95% Confidence Interval (CI) (1.1, 3.1) p = 0.03 and 2.9 (1.2, 7.1) p = 0.01 respectively, and with PSC cataract, OR = 1.5 (1.1, 2.2) p = 0.02 and 1.8 (0.9, 3.6) p = 0.07 respectively. There was no consistent association of SNPs with nuclear cataract or a combined variable of any type of cataract including operated cataract. Conclusions: Our results in the Indian population agree with previous studies of the association of EPHA2 variants with cortical cataracts. We report new findings for the association with PSC which is particularly prevalent in Indians

    1ST MEASUREMENT OF GAMMA(D(S)(+)-]MU+NU)/GAMMA(D(S)(+)-]PHI-PI+)

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    Complete Author List: ACOSTA D, ATHANAS M, MASEK G, PAAR H, BEAN A, GRONBERG J, KUTSCHKE R, MENARY S, MORRISON RJ, NAKANISHI S, NELSON HN, NELSON TK, RICHMAN JD, RYD A, TAJIMA H, SCHMIDT D, SPERKA D, WITHERELL MS, PROCARIO M, YANG S, BALEST R, CHO K, DAOUDI M, FORD WT, JOHNSON DR, LINGEL K, LOHNER M, RANKIN P, SMITH JG, ALEXANDER JP, BEBEK C, BERKELMAN K, BESSON D, BROWDER TE, CASSEL DG, CHO HA, COFFMAN DM, DRELL PS, EHRLICH R, GALIK RS, GARCIASCIVERES M, GEISER B, GITTELMAN B, GRAY SW, HARTILL DL, HELTSLEY BK, JONES CD, JONES SL, KANDASWAMY J, KATAYAMA N, KIM PC, KREINICK DL, LUDWIG GS, MASUI J, MEVISSEN J, MISTRY NB, NG CR, NORDBERG E, OGG M, PATTERSON JR, PETERSON D, RILEY D, SALMAN S, SAPPER M, WORDEN H, WURTHWEIN F, AVERY P, FREYBERGER A, RODRIGUEZ J, STEPHENS R, YELTON J, CINABRO D, HENDERSON S, KINOSHITA K, LIU T, SAULNIER M, SHEN F, WILSON R, YAMAMOTO H, ONG B, SELEN M, SADOFF AJ, AMMAR R, BALL S, BARINGER P, COPPAGE D, COPTY N, DAVIS R, HANCOCK N, KELLY M, KWAK N, LAM H, KUBOTA Y, LATTERY M, NELSON JK, PATTON S, PERTICONE D, POLING R, SAVINOV V, SCHRENK S, WANG R, ALAM MS, KIM IJ, NEMATI B, ONEILL JJ, SEVERINI H, SUN CR, ZOELLER MM, CRAWFORD G, DAUBENMIER CM, FULTON R, FUJINO D, GAN KK, HONSCHEID K, KAGAN H, KASS R, LEE J, MALCHOW R, MORROW F, SKOVPEN Y, SUNG M, WHITE C, WHITMORE J, WILSON P, BUTLER F, FU X, KALBFLEISCH G, LAMBRECHT M, ROSS WR, SKUBIC P, SNOW J, WANG PL, WOOD M, BORTOLETTO D, BROWN DN, FAST J, MCILWAIN RL, MIAO T, MILLER DH, MODESITT M, SCHAFFNER SF, SHIBATA EI, SHIPSEY IPJ, WANG PN, BATTLE M, ERNST J, KROHA H, ROBERTS S, SPARKS K, THORNDIKE EH, WANG CH, DOMINICK J, SANGHERA S, SHELKOV V, SKWARNICKI T, STROYNOWSKI R, VOLOBOUEV I, ZADOROZHNY P, ARTUSO M, HE D, GOLDBERG M, HORWITZ N, KENNETT R, MONETI GC, MUHEIM F, MUKHIN Y, PLAYFER S, ROZEN Y, STONE S, THULASIDAS M, VASSEUR G, ZHU G, BARTELT J, CSORNA SE, EGYED Z, JAIN V, SHELDON P, AKERIB DS, BARISH B, CHADHA M, CHAN S, COWEN DF, EIGEN G, MILLER JS, OGRADY C, URHEIM J, WEINSTEIN A

    "Closing the R&D Gap, Evaluating the Sources of R&D Spending"

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    Both spending and tax policies have been implemented in the United States with the goal of stimulating private sector research and development (R&D). Karier questions whether current R&D policy, especially the research and experimentation tax credit, can contribute to closing the gap between nondefense expenditures on R&D in the United States and such expenditures in other countries, such as Japan and Germany. He also explores possible changes to our current R&D policy to make it more effective.

    Vertex sparsifiers : new results from old techniques

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    Given a capacitated graph G=(V,E)G = (V,E) and a set of terminals KVK \subseteq V, how should we produce a graph HH only on the terminals KK so that every (multicommodity) flow between the terminals in GG could be supported in HH with low congestion, and vice versa? (Such a graph HH is called a flow sparsifier for GG.) What if we want HH to be a “simple” graph? What if we allow HH to be a convex combination of simple graphs? Improving on results of Moitra [Proceedings of the 50th IEEE Symposium on Foundations of Computer Science, IEEE Computer Society, Los Alamitos, CA, 2009, pp. 3--12] and Leighton and Moitra [Proceedings of the 42nd ACM Symposium on Theory of Computing, ACM, New York, 2010, pp. 47--56], we give efficient algorithms for constructing (a) a flow sparsifier HH that maintains congestion up to a factor of O(logkloglogk)O(\frac{\log k}{\log \log k}), where k=Kk = |K|; (b) a convex combination of trees over the terminals KK that maintains congestion up to a factor of O(logk)O(\log k); (c) for a planar graph GG, a convex combination of planar graphs that maintains congestion up to a constant factor. This requires us to give a new algorithm for the 0-extension problem, the first one in which the preimages of each terminal are connected in GG. Moreover, this result extends to minor-closed families of graphs. Our bounds immediately imply improved approximation guarantees for several terminal-based cut and ordering problems

    Gaps in intervals of N-expansions

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    For N ∈ N≥2 and α ∈ R such that 0 < α ≤ N − 1, the continued fraction map Tα: [α, α+1] → [α, α+1) is defined as Tα (x):= N/x−d(x), where d: [α, α+1] → N is defined by d(x):= ⌊N/x − α⌋. A maximal open interval (a, b) ⊂ Iα is called a gap of Iα if for almost every x ∈ Iα there is an n0 (x) ∈ N such that xn /∈ (a, b) for all n ≥ n0 . In this paper, all conditions are given in which Iα is gapless. For α =√N − 1 it is shown that the number of gaps is a finite, monotonically non-decreasing and unbounded function of N.Green Open Access added to TU Delft Institutional Repository ‘You share, we take care!’ – Taverne project https://www.openaccess.nl/en/you-share-we-take-care Otherwise as indicated in the copyright section: the publisher is the copyright holder of this work and the author uses the Dutch legislation to make this work public.Applied Probabilit

    Challenge in R&D Management : Tata Steel A Case Study

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    The purpose of R&D management is to promote innovation as well as wealth creation. The paper traces the history of R&D managementhow it has changed from the first generation when only innovation was the main objective to the fifth generation where IT plays an important role. It is now necessary to understand the needs of market for conducting worthwhile research. The author shares his experience of R&D management at Tata Steel. The experience shows that by adopting judicious R&D strategy it is possible to face the challenges of reconciling innovation with wealth creation is possible by a judicious R&D strategy

    A 2 h periodic variation in the low-mass X-ray binary Ser X-1

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    Spectroscopy of the low-mass X-ray binary Ser X-1 using the Gran Telescopio Canarias have revealed a ?2 h periodic variability that is present in the three strongest emission lines. We tentatively interpret this variability as due to orbital motion, making it the first indication of the orbital period of Ser X-1. Together with the fact that the emission lines are remarkably narrow, but still resolved, we show that a main-sequence K dwarf together with a canonical 1.4 M? neutron star gives a good description of the system. In this scenario, the most likely place for the emission lines to arise is the accretion disc, instead of a localized region in the binary (such as the irradiated surface or the stream-impact point), and their narrowness is due instead to the low inclination (?10°) of Ser X-1
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