Parallel capture

The default test protocol inferred by TC has four phases Scan Shift, Parallel Measure, Parallel Capture, and Scan-Out Strobe. Each test pattern has all these phases. The length of the scan shift phase is equal to the length of the longest scan chain in the design. The remaining three phases are of one cycle with the test clock being pulsed in only during scan shift and the parallel capture cycle. Shown below are the values of the bi-directionals in the different phases ... 

Use a strobe before the clock protocol. This protocol is automatically inferred by TC when the test default.strobe is set before the active clock edge. In this protocol file the parallel measure and the parallel capture cycles are combined into one. 

Use the TC variable, test no three state conflicts after capture to hold the values of the bi-directional ports in the parallel capture cycle from the parallel measure cycle. 

Eveiy test pattern consists of the following phases scan-shift, parallel measure, parallel capture, and scan-out strobe. You can add initialization vectors at the start of the test program using the read init protocol command. Shown below is the default protocol inferred by TC for a design after scan-insertion. 

In the default test protocol inferred by TC, the last scan cell in the scan chain is strobed in the scan-out strobe cycle after the parallel capture cycle. If this is not the case, the next scan-shift cycle will overwrite the captured response in the last scan cell before it is strobed. Hence in the last cycle of the scan shift there is no expected response, that is an X. 

In the default test protocol inferred by TC there is a separate scan-out strobe cycle after the parallel-capture cycle. Why is this cycle not merged with the parallel-capture cycle ... 

In 1974, Vogtle and Weber disclosed the preparation of a class of molecules which they reported showed remarkable phenomenological parallelisms to the mode of food capture by an octopus using its suction pads . Such molecules have also been referred to as hexa-hosts (see below). 

Illustrated in Figure 6, this engine incorporates a flat three-sided rotor captured between parallel end walls. The rotor orbits and rotates around the central shaft axis, and within a stationaiy housing that is specially... 

In terms of evolutionary biology, the complex mitotic process of higher animals and plants has evolved through a progression of steps from simple prokaryotic fission sequences. In prokaryotic cells, the two copies of replicated chromosomes become attached to specialized regions of the cell membrane and are separated by the slow intrusion of the membrane between them. In many primitive eukaryotes, the nuclear membrane participates in a similar process and remains intact the spindle microtubules are extranuclear but may indent the nuclear membrane to form parallel channels. In yeasts and diatoms, the nuclear membrane also remains intact, an intranuclear polar spindle forms and attaches at each pole to the nuclear envelope, and a single kinetochore microtubule moves each chromosome to a pole. In the cells of higher animals and plants, the mitotic spindle starts to form outside of the nucleus, the nuclear envelope breaks down, and the spindle microtubules are captured by chromosomes (Kubai, 1975 Heath, 1980 Alberts et al., 1989). 

The collision process can be captured by a high speed video camera as shown in Fig. 6 [14]. The slurry is about 50 mm apart away from the solid surface at 0 s (Fig. 6(a)), and reaches the surface at 0.018 s (Fig. 6(b)). Then the slurry reflects at an angle as same as the incidence angle (Fig. 6(c)). As time goes, the reflected liquid beam is divided into two beams, one is in the reflected direction and another is parallel to the solid surface as shown in Fig. 6(d). When time reaches 0.068 s, most of the reflected slurry moves along the solid surface. 

When compared to standard (open cavity) cone-plate or parallel disks rheometers, closed cavity torsional rheometers such as the RPA or the PPA have unique high-strain capabilities, which prompted us to modify the instmment in order to investigate the promises of FT rheometry, as outlined a few years ago by the pioneering works of Wilhelm. The technique consists of capturing strain and torque signals and in using FT calculation algorithms to resolve it into their harmonic components, as detailed below. 

The anatomical separation achieved by reptiles parallels the divergence of the main/accessory receptor categories. AOS chemoreception is assumed to elaborate its semiochemical responses by selective gains in ligand-capture efficiency and by alterations of threshold values. Once... 

These setups have been chosen to measure abundances of iron peak, a-elements and neutron-capture elements. In parallel, a subset of 14 stars has been observed with the high resolution spectrograph UVES (R=48000) to serve as calibrators for the GIRAFFE sample. 

The most striking feature observed in Sgr dSph is the presence of a metal rich ([Fe/H] between -1 and 0) and young population, showing the a-elements underabundance now recognized as typical of dSph (see [12]). Besides that, we observe a strong (up to 0.8 dex) overabundance of n-capture elements (La, Ce, Nd) with respect to iron, a significant Na and A1 under abundance, and an intriguing Ni deficiency. All these chemical features appear to be typical of Sgr dSph and of its associated systems like Terzan 7 and Pal 12 (e.g. [4]). Moreover, we observed an important underabundance of Zn ([Zn/Fe] -0.4). This may undermine the parallelism between dSph and the DLAs, where Zn is used as a proxy for Fe. 

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