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If you created a user account during the preceding installation and left Automatic Login selected when you created that account, openSUSE should automatically log you in as that user and present you with the KDE desktop. (If you are presented with a graphical login screen instead, log in as that user now.) Here are a few things to help you get started using openSUSE: Desktop applications The default openSUSE install is configured as a desktop system that includes a set of easily accessible desktop applications. On the desktop, try the Office icon to open OpenOffice.org to work with documents, spreadsheets, presentations, drawings, Web pages, or a variety of other content types. From the openSUSE icon on the panel, select from among dozens of applications to try them out. My Computer A My Computer icon on the desktop enables you to see removable media and mounted partitions, and also gives you access to your Desktop, Documents, and public_html folders in a Konqueror window. Reconfigure your computer Get to the YaST administration tool by selecting Applications System Administrator Settings from the openSUSE menu. You can reconfigure your system hardware and software from the YaST Control Center that appears. If you want to configure your desktop (change backgrounds, screen savers, or themes), use the KDE control center as you would with any modern KDE desktop. You can launch the control center from the openSUSE menu (select My Favorites Configure Desktop).

Each of the 21 markets in the CRB Index carries equal weight in the preceding formula, which means that each market contributes 1/21 (4.7%) to the Index's value. However, although each individual commodity market has equal weight in the CRB Index, this does not mean that each commodity group carries equal weight. Some commodity groups carry more weight than others. The following breakdown divides the CRB Index by groups to give a better idea how the weightings are distributed: MEATS: METALS: IMPORTED: ENERGY: GRAINS: INDUSTRIALS: Cattle, hogs, porkbellies (14.3%) Gold, platinum, silver (14.3%) Cocoa, coffee, sugar (14.3%) Crude oil, heating oil (9.5%) Corn, oats, wheat, soybeans, soybean meal, soybean oil (28.6%) Copper, cotton, lumber (14.3%)

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The .TS macro starts the table, and the next line indicates that the table should be centered on the page (center) and surrounded by a line box and that a colon will be used to separate the data into cells (tab(:)). The third line shows that the heading should be centered in the box (c) and should span across the next two cells (s s). The fourth line says that the heading of each cell should be centered (c | c | c) and the fifth line indicates that the data cells that follow should be left justified (l | l | l).

in which p and u stand for the particles (ions or molecules), 1 and m are the coordinates of these particles, and is the unit cell, located at a distance rg from the reference unit cell. The wave vector k is a measure of the phase shift between two neighboring unit cells (Sec. 4.5). With a modulus of 2n/X (A is the wavelength), k is practically zero in infrared and Raman spectra. Accordingly, the exponential term equals one, i.e., only motions in which the primitive unit cells vibrate in phase are observed. This was recognized early by Shimanouchi, who proposed an extension of the GF matrix method in order to calculate diamond, CaF2, and perovskite fluorides (Shimanouchi et al., 1961; Nakagawa et al., 1967). In the case of molecular crystals the problem may be simplified by treating the molecules as entities, since intermolecular and intramolecular potentials usually differ by several orders of magnitude. There are thus two possibilities. The first option, known as rigid-body approximation, operates only on the so-called lattice modes which are usually observed between 0 and 250 cm-' and which consist of translations and/or rotations (librations) of molecules around their equilibrium positions. Coupling of these degrees of freedom with internal motion is neglected. The second possibility is based on the assumption that molecules in a crystal remain unchanged. This option, on the one hand, utilizes the normal modes of the isolated molecule, on the other hand it employs the translations and vibrations as a basis for a complete treatment of the unit cell. This alternative allows coupling between internal and external degrees of freedom. The corresponding formalism has been developed by Caljfano, who also reviews some examples (Califano, 1976).

{={1,2,3,4;5,6,7,8;9,10,11,12}*2}

Reactive absorption is usually carried out in apparata providing a continuous flow of both contacting phases. Reactive absorption units can be best classified if one considers which of the phases is in a continuous form, and which is in a disperse form. Using this criterion, the classification of the reactive absorption equipment is represented in Tab. 9.2 (see Ref. [1]). Most often, reactive absorption is carried out in packed or plate columns. The structure of such columns and different internals are shown schematically in Fig. 9.2. Packed columns are commonly used in reactive absorption operations [10, 11]. They represent cylindrical or rectangular columns up to several meters in diameter

if(( errors == null) || (errors.isEmpty()) ) { if(actionMapping.getAttribute() != null) { if ( request .equals(actionMapping.getScope())) request.removeAttribute(actionMapping.getAttribute()); else session.removeAttribute(actionMapping.getAttribute()); } return actionMapping.findForward( success ); } else { saveErrors(request, errors); return new ActionForward(actionMapping.getInput()); } } }

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