Deposits of clastic carbonate-dominated (calciclastic) sedimentary slope systems in the rock record have been identified mostly as linearly-consistent carbonate apron deposits, even though most ancient clastic carbonate slope deposits fit the submarine fan systems better. Calciclastic submarine fans are consequently rarely described and are poorly understood. Subsequently, very little is known especially in mud-dominated calciclastic submarine fan systems. Presented in this study are a sedimentological core and petrographic characterisation of samples from eleven boreholes from the Lower Carboniferous of Bowland Basin (Northwest England) that reveals a >250 m thick calciturbidite complex deposited in a calciclastic submarine fan setting. Seven facies are recognised from core and thin section characterisation and are grouped into three carbonate turbidite sequences. They include: 1) Calciturbidites, comprising mostly of highto low-density, wavy-laminated bioclast-rich facies; 2) low-density densite mudstones which are characterised by planar laminated and unlaminated muddominated facies; and 3) Calcidebrites which are muddy or hyper-concentrated debrisflow deposits occurring as poorly-sorted, chaotic, mud-supported floatstones. These

Phd by thesis

This paper describes the contents of the 2016 edition of the HITRAN molecular spectroscopic compilation. The new edition replaces the previous HITRAN edition of 2012 and its updates during the intervening years. The HITRAN molecular absorption compilation is composed of five major components: the traditional line-by-line spectroscopic parameters required for high-resolution radiative-transfer codes, infrared absorption cross-sections for molecules not yet amenable to representation in a line-by-line form, collision-induced absorption data, aerosol indices of refraction, and general tables such as partition sums that apply globally to the data. The new HITRAN is greatly extended in terms of accuracy, spectral coverage, additional absorption phenomena, added line-shape formalisms, and validity. Moreover, molecules, isotopologues, and perturbing gases have been added that address the issues of atmospheres beyond the Earth. Of considerable note, experimental IR cross-sections for almost 300 additional molecules important in different areas of atmospheric science have been added to the database. The compilation can be accessed through www.hitran.org. Most of the HITRAN data have now been cast into an underlying relational database structure that offers many advantages over the long-standing sequential text-based structure. The new structure empowers the user in many ways. It enables the incorporation of an extended set of fundamental parameters per transition, sophisticated line-shape formalisms, easy user-defined output formats, and very convenient searching, filtering, and plotting of data. A powerful application programming interface making use of structured query language (SQL) features for higher-level applications of HITRAN is also provided.

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The HITRAN 2008 molecular spectroscopic database

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Table Of Integrals Series And Products

Tables of integrals

Climate Change 1995 is a scientific assessment that was generated by more than 1 000 contributors from over 50 nations. It was jointly co-ordinated through two international agencies; the World Meteorological Organization and the United Nations Environment Programme. The assessment was completed by the Intergovernmental Panel on Climate Change (IPCC) with a primary aim of reviewing the current state of knowledge concerning the impacts of climate change on physical and ecological systems, human health, and socioeconomic factors. The second aim was to review the available information on the technical and economic feasibility of the potential mitigation and adaptation strategies.

Climate Change 1995

Calculation of electron impact total and ionization cross sections for Sr, Y, Ru, Pd, and Ag atoms were performed using spherical complex optical potential and complex scattering potential-ionization contribution methods. The complex optical potential model is formulated from the target parameters and the atomic charge density. The spherical charge densities are in turn derived from the Roothaan–Hartree–Fock wavefunctions defining the atomic orbital of the target. In the present study cross sections are computed in the energy range from ionization threshold to 2000 eV. The results obtained are compared with other theories and measurements wherever available and were found to be quite consistent and uniform. In general, present data show an overall reasonable agreement with other results. Dependence of total cross sections on the number of target electrons and peak of ionization cross section on target parameters were also found to be consistent with previous observations.

Electron impact total and ionization cross sections for Sr, Y, Ru, Pd, and Ag atoms

The charge transport mechanisms of Hg contact on n-type silicon crystal having 〈1 0 0〉 orientation were investigated in the temperature range of 160–293 K by the thermionic emission theory. The temperature variation of barrier height and ideality factor illustrates an inhomogeneous interface with a Gaussian barrier height distribution. The plots of temperature dependent zero-bias barrier height, ideality factor, series resistance and reverse leakage current show a discontinuity below 240 K. The experimental barrier height and ideality factor versus 1/T plot gives two slopes, one in the 160–220 K region and the other in the 240–293 K region, thereby revealing a double Gaussian distribution of barrier heights. The observed discontinuity in the diode parameters and the existence of double Gaussian barrier heights are interpreted on the basis of phase transition of mercury from its liquid state to solid form.

Phase transition induced double-Gaussian barrier height distribution in Schottky diode

The present paper reports ionisation, elastic and total cross section for the first three members of dimethyl sulphide, dimethyl disulphide and dimethyl sulphoxide family of molecules. The multi-scattering centre spherical complex optical potential formalism is applied for integral elastic and inelastic cross section calculations. From the inelastic part, ionisation cross section is derived using complex scattering potential-ionisation contribution method. The total cross section is then obtained from the sum of elastic and inelastic contributions. A reasonably good agreement is obtained for elastic cross section, wherever comparison is available. The ionisation and total cross section calculation for the complete set of molecules has been performed for the first time.

Bobby Antony

Papers

Electron impact total and ionization cross sections for Sr, Y, Ru, Pd, and Ag atoms

Phase transition induced double-Gaussian barrier height distribution in Schottky diode

Electron scattering studies of DMS, DMDS and DMSO homologous series

Electron scattering from C2-C8 symmetric ether molecules

Electron impact total ionization cross section for C 4 and C 5 isomeric alcohols