64,020 research outputs found
A 2 h periodic variation in the low-mass X-ray binary Ser X-1
No full textSpectroscopy 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
Evidence for the decay B0→J/ψω and measurement of the relative branching fractions of meson decays to J/ψη and J/ψη′
Get PDFFirst evidence of the B 0 → J / ψ ω decay is found and the B s 0 → J / ψ η and B s 0 → J / ψ η ′ decays are studied using a dataset corresponding to an integrated luminosity of 1.0 fb -1 collected by the LHCb experiment in proton-proton collisions at a centre-of-mass energy of sqrt(s) = 7 TeV. The branching fractions of these decays are measured relative to that of the B 0 → J / ψ ρ 0 decay:frac(B (B 0 → J / ψ ω), B (B 0 → J / ψ ρ 0)) = 0.89 ± 0.19 (stat) - 0.13 + 0.07 (syst),frac(B (B s 0 → J / ψ η), B (B 0 → J / ψ ρ 0)) = 14.0 ± 1.2 (stat) - 1.5 + 1.1 (syst) - 1.0 + 1.1 (frac(f d, f s)),frac(B (B s 0 → J / ψ η ′), B (B 0 → J / ψ ρ 0)) = 12.7 ± 1.1 (stat) - 1.3 + 0.5 (syst) - 0.9 + 1.0 (frac(f d, f s)), where the last uncertainty is due to the knowledge of f d / f s, the ratio of b-quark hadronization factors that accounts for the different production rate of B 0 and B s 0 mesons. The ratio of the branching fractions of B s 0 → J / ψ η ′ and B s 0 → J / ψ η decays is measured to befrac(B (B s 0 → J / ψ η ′), B (B s 0 → J / ψ η)) = 0.90 ± 0.09 (stat) - 0.02 + 0.06 (syst)
Catalytic P-H activation by Ti and Zr catalysts
No full textCatalytic dehydrocoupling of phosphines was investigated using the anionic zirconocene trihydride salts [Cp*Zr-2(mu-H)(3)Li](3) (1a) or [Cp*Zr-2(mu-H)(3)K(thf)(4)] (1b), and the metallocycles [CpTi(NPtBu3)(CH2)(4)] (6) and [Cp*M(NPtBu3)(CH2)(4)] (M = Ti 20, Zr 21) as catalyst precursors. Dehydrocoupling of primary phosphines RPH2 (R = Ph, C6H2Me3, Cy, C10H7) gave both dehydrocoupled dimers RP(H)P(H)R or cyclic oligophosphines (RP)(n) (n = 4, 5) while reaction of tBu(3)C(6)H(2)PH(2) gave the phosphaindoline tBu(2)(Me2CCH2)C6H2PH (9). Stoichiometric reactions of these catalyst precursors with primary phosphines afforded [Cp*Zr-2((PR)(2))H][K(thf)(4)] (R = Ph 2, Cy 3, C6H2Me3 4), [Cp*Zr-2((PPh)(3))H] [K(thf)(4)] (5), [CpTi(NPtBu3)(PPh)(3)] (7) and [CpTi(NPtBu3)(mu-PHPh)](2) (8), while reaction of 6 with (C(6)H(2)tBu3)PH2 in the presence of PMe3 afforded [CpTi(NPtBu3)(PMe3)(p(C(6)H(2)tBu(3))] (10). The secondary phosphines Ph2PH and (PhHPCH2)(2)CH2 also undergo dehydrocoupling affording (Ph2P)(2) and (PhPCH2)(2)CH2. The bisphosphines (CH2PH2)(2) and C6H4(PH2)(2) are dehydrocoupled to give (PCH2CH2PH)(2) (12) and (C6H4P(PH))(2) (13) while prolonged reaction of 13 gave (C6H4P2)(8) (14). The analogous bisphosphine Me2C6H4(PH)(2) (17) was prepared and dehydrocoupling catalysis afforded (Me2C6H2P(PH))(2) (18) and subsequently [(Me2C6H2P2)(2)(mu-Me2C6H2P2)](2) (19). Stoichiometric reactions with these bisphosphines gave [Cp*Zr-2(H)(PH)(2)C6H4] [Li(thf)(4)] (22), [Cp*Ti(NPtBu3)(PH)(2)C6H4](2) (23) and [Cp*Ti(NPtBu3)(PH)(2)C6H4] (24). 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Salix diazii M. Idrees & J. M. H. Shaw 1015, nom. nov.
No full textSalix × diazii M. Idrees & J.M.H. Shaw, nom. nov. Replaced name:— Salix × longissima T.E.Díaz & J.Andrés (1987: 132), nom. illeg., non S. longissima P.Wessel (1855: 140). Type:— SPAIN. Léon Province: La Martina, 490 m, 29TPH91, 16 June 1985, T.E. Díaz et al. s.n. (holotype, LEB29538!, isotypes LEB29539!, LEB30605!). Etymology:— The specific epithet honours Prof. Dr. Tomás Emilio Díaz González (University of Oviedo, Oviedo, Spain), author of the replaced name, for his tremendous contributions to the taxonomy of the genus Salix. Distribution:— Spain, Léon Province (La Martina).Published as part of Idrees, Muhammad & Shaw, Julian M. H., 2022, A new name for extant Salix × longissima T. E. Díaz & J. Andrés (Salicaceae), pp. 213-214 in Phytotaxa 550 (2) on page 213, DOI: 10.11646/phytotaxa.550.2.11, http://zenodo.org/record/664103
Christian nonconformity by J. H. Yoder and M. L. King
Get PDFThis Bachelor thesis with the title Christian nonconformity by J. H. Yoder and M. L. King, deals with the specific status of Christian in society. The first part of the thesis is dedicated to the ethical concept of J. H. Yoder and the second part is dedicated to the ethical concept of M. L. King. The final part is attempting to compare both approaches with a focus on nonconformity. In the comparison is persuaded the social aspect in particular and shows the relationship between the society and the Christians according both concepts. The author of the work uses as literal sources particularly the essays and speeches from M. L. King and from the book of J. H. Yodera: The politics of Jesus. Powered by TCPDF (www.tcpdf.org
Transformation of the endostyle of the anadromous sea lamprey, Petromyzon-marinus L, during metamorphosis .2. Electron-microscopy
No full textPT: J; CR: BARRINGTON EJW, 1956, Q J MICROSC SCI, V97, P393 BARRINGTON EJW, 1975, INTRO GENERAL COMP E BEAMISH FWH, 1975, J ZOOL, V177, P57 BENCOSME SA, 1959, J BIOPHYS BIOCHEM CY, V5, P508 CHENG H, 1974, AM J ANAT, V141, P537 CLEMENTSMERLINI M, 1960, J MORPHOL, V106, P337 COLEMAN R, 1968, GEN COMP ENDOCR, V10, P34 CORDIER AC, 1976, AM J ANAT, V146, P339 DAEMS WT, 1969, LYSOSOMES, V1, P64 EGEBERG J, 1965, Z ZELLFORSCH MIKROSK, V68, P102 ETKIN W, 1968, METAMORPHOSIS PROBLE, P313 FINSTAD J, 1964, J EXP MED, V120, P1151 FOX H, 1970, J EMBRYOL EXP MORPH, V24, P139 FOX H, 1973, Z ZELLFORSCH, V130, P371 FUJITA H, 1966, Z ZELLFORSCH MIKROSK, V73, P559 FUJITA H, 1968, GEN COMP ENDOCR, V11, P111 FUJITA H, 1969, Z ZELLFORSCH, V98, P525 FUJITA H, 1972, ARCH HISTOL JAPON, V34, P109 FUJITA H, 1975, ARCH HISTOL JPN, V37, P277 FUJITA H, 1975, INT REV CYTOL, V40, P197 GOOD RA, 1972, BIOL LAMPREYS, V2, P405 GORBMAN A, 1962, TXB COMP ENDOCRINOLO HELMINEN HJ, 1971, J ULTRASTRUCT RES, V36, P708 HENDERSON NE, 1971, GEN COMP ENDOCR, V16, P409 HILFER SR, 1964, J MORPHOL, V115, P135 HILFER SR, 1977, J CELL BIOL, V75, P446 HOHEISEL G, 1969, GEGENBAURS MORPHOL J, V114, P204 HOHEISEL G, 1970, MORPHOL JB, V114, P337 HOURDRY J, 1969, Z ZELLFORSCH MIKR AN, V101, P527 JAMIESON JD, 1977, INT CELL BIOL, P308 KLINCK GH, 1970, LAB INVEST, V22, P2 KRAENVZEL F, 1933, ARCH BIOL LIEGE, V44, P469 KRUPP PP, 1977, ANAT REC, V187, P495 LANZING WJR, 1959, STUDIES RIVER LAMPRE LEACH JW, 1939, J MORPHOL, V65, P549 LUFT JH, 1961, J BIOPHYS BIOCH CYTO, V9, P409 MANASEK FJ, 1969, J EMBRYOL EXP MORPH, V21, P271 MARINE D, 1913, J EXP MED, V17, P379 MILLONIG G, 1961, J APPL PHYS, V32, P1637 MOLLENHAUER HH, 1964, STAIN TECHNOL, V39, P111 MORRIS GP, 1979, CELL TISSUE RES, V196, P449 NEUENSCHWANDER P, 1972, Z ZELLFORSCH MIKROSK, V130, P553 NEVE P, 1965, J MICROSC-PARIS, V4, P811 NICKERSON PA, 1970, J CELL BIOL, V47, P277 NOVIKOFF AB, 1976, CELLS ORGANELLES NUNEZ EA, 1967, J CELL BIOL, V2, P404 NUNEZ EA, 1976, ANAT REC, V184, P133 OLIN P, 1970, ENDOCRINOLOGY, V87, P1000 OLIVEREAU M, 1952, ARCH ANAT MICROSC EX, V41, P1 OOI EC, 1976, CAN J ZOOL, V54, P1449 OOI EC, 1979, AM J ANAT, V154, P57 PEEK WD, 1979, J MORPHOL, V160, P143 PIPAN N, 1976, CYTOBIOLOGIE, V13, P435 POLLARD B, 1966, PHYLOGENY IMMUNITY, P88 REMY L, 1977, J ULTRASTRUCT RES, V61, P243 REYNOLDS ES, 1963, J CELL BIOL, V17, P208 ROITT IM, 1971, ESSENTIAL IMMUNOLOGY, P211 ROMERT P, 1973, Z ANAT ENTWICKLUNGS, V139, P319 SELJELID R, 1967, J ULTRASTRUCT RES, V17, P195 SELJELID R, 1967, J ULTRASTRUCT RES, V17, P401 SETOGUTI T, 1973, Z ZELLFORSCH MIKROSK, V137, P195 SHEPARD TH, 1967, J CLIN ENDOCR METAB, V27, P945 SHIVELY JN, 1969, AM J VET RES, V30, P219 STERBA G, 1953, WISS Z F SCHILLER MN, V3, P1 STERBA G, 1953, WISS Z F SCHILLER MN, V3, P239 STERBA G, 1961, INT REV GES HYDROBIO, V46, P105 STERBA G, 1962, HDB BINNENFISCHEREI, V3, P263 THIELE J, 1976, CELL TISSUE RES, V168, P133 WATSON ML, 1958, J BIOPHYS BIOCHEM CY, V4, P475 WESSELLS NK, 1971, SCIENCE, V171, P135 WETZEL BK, 1969, ENDOCRINOLOGY, V84, P563 WISSIG SL, 1960, J BIOPHYS BIOCHEM CY, V7, P419 WOLLMAN SH, 1969, LYSOSOMES BIOLOGY PA, V2, P483 WRIGHT G, 1978, AM J ANAT, V152, P263 WRIGHT GM, 1976, GEN COMP ENDOCR, V30, P243 WRIGHT GM, 1977, J EXP ZOOL, V202, P27 WRIGHT GM, 1978, THESIS U TORONTO, P70 YOUSON JH, 1977, CAN J ZOOL, V55, P469 YOUSON JH, 1979, CAN J ZOOL, V57, P1808 YOUSON JH, 1980, CAN J FISH AQUAT SCI, V37; NR: 80; TC: 21; J9: J MORPHOL; PG: 27; GA: KT943Source type: Electronic(1
Analysis & development of automated system for on-wafer channel thermal measurement of RF power devices using ordinary lab instruments
Get PDFAccurate and precise measurement of channel temperature for RF devices and especially for high power density devices such as MESFETs and GaAs High Electron Mobility Transistors (HEMTs) is essential for understanding the physics behind device degradation. In high power density devices, self-heating effects (SHEs) and channel to base plate temperature gradients are very high. This paper proposes an automated experimental setup using ordinary lab instruments for the measurement of channel temperature of MESFETs and HEMTs in terms of thermal resistance (θth) and thermal capacitance (Cth). The automated experimental setups utilize ordinary lab equipment instead of using specialized high-end tools. With ambient temperature, DC bias conditions, and RF power levels, channel temperature is calculated using θth and Cth parameters. The proposed technique is applied on three different HEMTs and the results were similar for all of them which reflect accuracy of the technique
Mesophilic-hydrothermal-thermophilic (M-H-T) digestion of green corn straw
No full textMesophilic-hydrothermal (80-160 degrees C, 30 min)-thermophilic (M-H-T) digestion and control tests of mesophilic (M), thermophilic (T), hydrothermal-mesophilic (H-M), and mesophilic-thermophilic digestion (M-T) of green corn straw were conducted for a 20-day fermentation period. The results indicate that M-H-T is an efficient method to improve methane production. A maximum methane yield of 371.74 mL/g volatile solid was obtained by the M (3 days)-H (140 degrees C)-T (17 days) process, which was 20.44%, 16.55%, 31.44%, and 14.31% higher than the yields of the M, T, 140-M, and M-T processes. The enhanced methane production was attributed to (1) the improved hemicellulose degradation and lignin disorganization; (2) prevention of the degradation of soluble sugar, easily hydrolyzed hemicellulose and cellulose into furfural and methylfurfural; and (3) lack of formation of Maillard reaction products during initial hydrothermal treatment. (C) 2015 Elsevier Ltd. All rights reserved
Measurement of the time-dependent CP asymmetry in B0 -> J/ψ KS0 decays
Get PDFThis Letter reports a measurement of the CP violation observables SJ/ψK0S and CJ/ψK0S in the decay channel B0→J/ψK0S performed with 1.0 fb−1 of pp collisions at s√=7 TeV collected by the LHCb experiment. The fit to the data yields SJ/ψK0S=0.73±0.07(stat)±0.04(syst) and CJ/ψK0S=0.03±0.09(stat)±0.01(syst). Both values are consistent with the current world averages and within
expectations from the Standard Model
Addition of arylchlorocarbenes to .alpha.,.beta.-unsaturated esters. Absolute rates, substituent effects, and variable reactivities
No full textPT: J; CR: BALASUBRAMANIYA.V, 1983, TETRAHEDRON, V39, P1475 BEENS H, 1967, J CHEM PHYS, V47, P1183 BERSON JA, 1974, J AM CHEM SOC, V96, P6175 BERSON JA, 1974, J AM CHEM SOC, V96, P6177 BOWMAN RM, 1974, J AM CHEM SOC, V96, P692 BROWN WG, 1966, J AM CHEM SOC, V88, P233 CALDWELL RA, 1978, J AM CHEM SOC, V100, P2905 COX DP, 1983, TETRAHEDRON LETT, V24, P5313 CREED D, 1976, J AM CHEM SOC, V98, P621 DEHMLOW EV, 1984, ANGEW CHEM INT EDIT, V23, P706 DOYLE MP, 1984, TETRAHEDRON LETT, V25, P901 DOYLE MP, 1986, TETRAHEDRON LETT, V27, P4395 DOYLE MP, 1987, CHEM DIAZIRINES, CH8 GILBERT WI, 1939, J ORG CHEM, V3, P611 GORDON M, 1975, EXCIPLEX GRAHAM WH, 1965, J AM CHEM SOC, V87, P4396 HOUK KN, 1984, J AM CHEM SOC, V106, P4293 HOUK KN, 1985, TETRAHEDRON, V41, P1555 HUISGEN R, 1963, ANGEW CHEM INT EDIT, V2, P633 KNIBBE H, 1967, J CHEM PHYS, V47, P184 KWIE WW, 1963, TETRAHEDRON LETT, P405 LAMBERT JB, 1983, TETRAHEDRON LETT, V24, P3799 LEONHARDT H, 1963, BER BUNSEN PHYS CHEM, V63, P791 LIU MTH, 1987, CHEM DIAZIRINES, CH5 LIU MTH, 1987, J ORG CHEM, V52, P323 LIU MTH, 1987, J ORG CHEM, V52, P4223 LIU MTH, 1987, TETRAHEDRON LETT, V28, P1011 LOUTFY RO, 1969, J AM CHEM SOC, V91, P3984 MOSS RA, 1967, TETRAHEDRON LETT, P4905 MOSS RA, 1969, J ORG CHEM, V34, P2220 MOSS RA, 1970, J AM CHEM SOC, V92, P6951 MOSS RA, 1977, J AM CHEM SOC, V99, P4105 MOSS RA, 1979, J AM CHEM SOC, V101, P5088 MOSS RA, 1979, TETRAHEDRON LETT, P4721 MOSS RA, 1980, ACCOUNTS CHEM RES, V13, P58 MOSS RA, 1985, REACTIVE INTERMEDIAT, V3, CH3 MOSS RA, 1986, J AM CHEM SOC, V108, P7028 MOSS RA, 1987, TETRAHEDRON LETT, V28, P4779 NAZAKI K, 1941, J AM CHEM SOC, V63, P2585 OKADA T, 1968, J CHEM PHYS, V49, P4717 RONDAN NG, 1980, J AM CHEM SOC, V102, P1770 SAKAI M, 1977, B CHEM SOC JP, V50, P1232 SAUER J, 1967, ANGEW CHEM INT EDIT, V6, P16 SCHOELLER WW, 1982, ANGEW CHEM INT ED EN, V12, P932 SKELL PS, 1969, J AM CHEM SOC, V91, P7131 TANIGUCHI Y, 1972, CHEM PHYS LETT, V13, P596 TURRO NJ, 1980, J AM CHEM SOC, V102, P7578 TURRO NJ, 1982, J AM CHEM SOC, V104, P1754 TURRO NJ, 1987, J AM CHEM SOC, V109, P4973 VAN SP, 1978, J AM CHEM SOC, V100, P3895 YANG NC, 1968, J AM CHEM SOC, V90, P5654; NR: 51; TC: 66; J9: J AMER CHEM SOC; PG: 10; GA: Q6555Source type: Electronic(1
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