290 research outputs found

    Bis(μ-quinoline-2-carboxyl­ato)-κ3 N,O:O;κ3 O:N,O-bis­[(acetato-κ2 O,O′)(methanol-κO)lead(II)]

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    The dinuclear title compound, [Pb2(C10H6NO2)2(CH3COO)2(CH3OH)2], lies across an inversion center. The methanol-coordinated PbII atom is chelated by the acetate anion as well as by the quinoline-2-carboxyl­ate anion. One O atom of the quinoline-2-carboxyl­ate anion bridges two symmetry-related PbII atoms, forming the dinuclear compound. Aside from the six atoms connected to the PbII atom by regular coordination bonds, the structure features a long Pb⋯O inter­action [3.145 (3) Å] that gives rise to a distorted Ψ-square-anti­prismatic geometry at the metal center. The H atom of the methanol is hydrogen bonded to an O atom of the acetate

    8-Hydr­oxy-2-methyl­quinolinium tetra­chlorido(quinolin-8-olato-κ2 N,O)stannate(IV) acetonitrile monosolvate

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    In the title solvated salt, (C10H10NO)[SnCl4(C9H6NO)]·CH3CN, the SnIV atom is chelated by the N,O-bidentate 8-hydroxy­quinolinate ligand and four chloride ions, generating a distorted SnONCl4 octa­hedral coordination geometry for the metal. In the crystal, the cations are linked to the anions and the solvent mol­ecules by O—H⋯O and N—H⋯N hydrogen bonds, respectively

    Numerical modeling of sedimentation in the Sefid-Rood Reservoir, Iran

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    River morphodynamics and sediment transportSedimentation in reservoir

    Super-simple (v,5,2)(v,5,2) directed designs and their smallest defining sets with its application in LDPC codes

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    In this paper, we show that for all v0,1v\equiv 0,1 (mod 5) and v15v\geq 15, there exists a super-simple (v,5,2)(v,5,2) directed design, also for these parameters there exists a super-simple (v,5,2)(v,5,2) directed design such that its smallest defining sets contain at least half of its blocks. Also, we show that these designs are useful in constructing parity-check matrices of LDPC codes.Comment: arXiv admin note: substantial text overlap with arXiv:1508.0009

    First report of simultaneous assessment of hepatitis A virus and hepatitis E virus seroprevalence among soldiers in Iran

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    Hepatitis E virus (HEV) and Hepatitis A virus (HAV) have been considered as common causes of viral hepatitis to military service members since their discovery. Although Iran has been recognized as an endemic country for HAV and HEV there is no study about HAV and HEV simultaneous prevalence among Iranian soldiers. The purpose of this study was to assess anti-HAV and anti-HEV antibodies in Iranian soldiers concurrently. In this cross-sectional study, a total of 400 serum samples were collected by simple random sampling for detection of anti-HAV and anti-HEV IgG by commercial HEV enzyme-linked immunosorbent assay (ELISA) kit. Out of 400 individuals, all participants were male with ages ranging from 18 to 26 years. Totally, 12% and 0.5% of the tested specimens were positive for anti-HAV and anti-HEV respectively. There were no significant differences between the subjects grouped according to age groups. Our finding presented a dramatic decrease in seropositivity against HAV. Therefore, vaccination for HAV should be reevaluated for military services in Iran

    Bis(acetato-κO)bis­(μ3-quinolin-8-olato-κ4 N,O:O:O)tetra­kis(μ2-quinolin-8-olato-κ3 N,O:O)tetra­zinc(II) dihydrate

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    In the centrosymmetric title compound, [Zn4(C9H6NO)6(C2H3O2)2]·2H2O, the ZnII atom that is bonded to one O atom of the acetate group is chelated by a quinolin-8-olate anion. This Zn atom is also bonded to the oxide O atoms of two other quinolin-8-olate anions, which themselves engage in chelation to the other ZnII atoms. The ZnII atom is five-coordinate in a square-pyramidal coordination geometry. The second ZnII atom is six-coordinate as it is linked to two oxide O atoms of the anions that chelate to the acetate-bound metal atom, and is chelated by two quinolin-8-olate ligands. The uncoordinated water mol­ecule is disordered over two positions in a 4:1 ratio. O—H⋯O hydrogen bonds between the water molecules and the free O atoms of the carboxylate groups consolidate the crystal packing

    Seasonal Variation of Earthworm Abundances and Biomass in Natural Forests and Plantations (North of Iran)

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    Soil productivity and plant growth are usually affected by biological activities of earthworms. The objective of this study was a comparative evaluation of earthworm abundances in 20-year-old plantations of Alder, Oak, Maple and Cypress with the adjacent natural mixed broad-leaved deciduous forest in the Caspian region of Iran. In this research one sample plot, each 1 ha; was selected in every plantation as well as in the natural stand, more over, in each plot, 10 microsample plots 10?10m were selected random systematically. To determine the seasonal variation of density and biomass with two methods, twenty samples were taken from each microsample plot. In the first method, 10 assigned soil pits of 100?100 cm and 30 cm depth were located among each treatment and adult earthworms were collected by hand counting. In the second method, 10 circular soil samples of 81cm2 to depth of 30 cm were taken in each treatment. The larves of earthworm extracted by using Berlese funnel and were counted by binocular. Finally in four seasons a total of 400 specimens were taken from 50 microsamples in different treatments. Moreover, some site and treatment parameters were measured in each plot. The abundance and biomass of earthworms in the Cypress plantation with 148.4 (n/m2) and 4.74 (g/m2) was significantly lower than other treatments, while the differences between other treatments were not statistically significant. The two important factors were extracted from eight variables in Factore analysis. The analysis of FA showed that some treatment parameters and nutritional values of litter take an important role in seasonal variation of earthworm abundance at all the treatments
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