Complete traversal

Secretory proteins and proteins destined for membranes distal to the ER completely traverse the membrane bilayer and are discharged into the lumen of the ER. 7V-Glycan chains, if present, are added (Chapter 47) as these proteins traverse the irmer part of the ER membrane—a process called cotranslational glycosyla-tion. Subsequently, the proteins are found in the... 

Figure 1. Biogeochemical C cycle, showing principal C reservoirs (boxes) in the mantle, crast, oceans and atmosphere, and showing the processes (arrows) that imite these reservoirs. The range of each of these reservoir boxes along the horizontal axis gives a visual estimate of values most typical of each reservoir. The vertical bars at right indicate the timeframes within which C typically completely traverses each of the four C sub-cycles (the HAB, SED, MET and MAN sub-cycles, see text). For example, C can traverse the hydrosphere-atmosphere-biosphere (HAB) sub-cycle typically in the time scale between 0 to 1000 years.

Circuit One complete traverse of the fiber feed mechanism of a filament winding machine. 

Single-circuit pattern Filament path makes a complete traverse of the chamber/mandrel, after which the following traverse lies immediately adjacent to the previous one. 

Circular linkage Pointers permitting more than one complete traversal of a data structure. 

In Table 2 we report the CPU time required by the various phases of the traversal procedure to complete traversal on the same set of circuit of Table 1. 

Circuit n. In filament winding, one complete traverse of the fiber-feed mechanism of the winding machine or a complete traverse of a winding band from one arbitrary point along the winding path to another point on a plane through the starting point and perpendicular to the axis. 

It is furthermore assumed that the release coefficient, (a), is a non-zero constant for the cell which has been completely traversed by the fluid (fresh water) and is zero for the remaining cells. Expressing it mathematically, for... 

Optical waveguide methods (188,196-198) are based on the phase shift associated with multiple interfacial reflections when either the s- orp-wave undergoes a total phase shift equal to an integral multiple of 2jt upon one complete traversal of a planar, dielectric waveguide sandwiched between media of lower refractive index, a standing wave is excited in the waveguiding film. Because of their dependence on reflection, the phase shifts are sensitive to interfacial heterogeneity—and the thickness, refractive index, and density of an adsorbed biomolecular layer can be readily determined. 

The full description of all the possible objects and their mutual relationships is complete once the tree has been completely traversed in an upward direction. The structure is now fully mapped onto hierarchically ordered computer data records containing complete information on nameable structural fragments present in the structure. The data records are related to one another by a system of pointers organised as an easily manageable ordered binary tree. 

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