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Adaptation, transient

A. J. Beumont, A. D. Noble, and A. Scariobrick, "Adaptive Transient Ah Euel Ratio Control to Minimise Gasoline Engine Emissions," Fisita Congress, London, 1992. [Pg.497]

The low MW power levels conuuonly employed in TREPR spectroscopy do not require any precautions to avoid detector overload and, therefore, the fiill time development of the transient magnetization is obtained undiminished by any MW detection deadtime. (3) Standard CW EPR equipment can be used for TREPR requiring only moderate efforts to adapt the MW detection part of the spectrometer for the observation of the transient response to a pulsed light excitation with high time resolution. (4) TREPR spectroscopy proved to be a suitable teclmique for observing a variety of spin coherence phenomena, such as transient nutations [16], quantum beats [17] and nuclear modulations [18], that have been usefi.il to interpret EPR data on light-mduced spm-correlated radical pairs. [Pg.1566]

The methods diseussed so far, fluoreseenee upeonversion, the various pump-probe speetroseopies, and the polarized variations for the measurement of anisotropy, are essentially eonventional speetroseopies adapted to the femtoseeond regime. At the simplest level of interpretation, the infonnation eontent of these eonventional time-resolved methods pertains to populations in resonantly prepared or probed states. As applied to ehemieal kineties, for most slow reaetions (on the ten pieoseeond and longer time seales), populations adequately speeify the position of the reaetion eoordinate intemiediates and produets show up as time-delayed speetral entities, and assignment of the transient speetra to ehemieal stnietures follows, in most oases, the same prinoiples used in speotrosoopio experiments perfomied with oontinuous wave or nanoseoond pulsed lasers. [Pg.1984]

Figure C3.1.3. Schematic diagram of Jouie heating T -jump apparatus for transient spectroscopy. (Adapted from French T C and Hammes G G i969 hdethods Enzymol. 16 3.)... Figure C3.1.3. Schematic diagram of Jouie heating T -jump apparatus for transient spectroscopy. (Adapted from French T C and Hammes G G i969 hdethods Enzymol. 16 3.)...
Table 6. -4 List of BWR Transient Initiating Events (adapted from NUREG-230Qj ... Table 6. -4 List of BWR Transient Initiating Events (adapted from NUREG-230Qj ...
Both the heat and cold shock response are universal and have been studied extensively. The major heat shock proteins (HSPs) are highly conserved. They are involved in the homeostatic adaptation of cells to harsh environmental conditions. Some act as molecular chaperones for protein folding, while others are involved in the processing of denatured polypeptides whose accumulation would be deleterious. The cold shock results in the transient induction of cold shock proteins (CSPs), which include a family of small acidic proteins carrying the cold shock domain. The CSPs appear to be involved in various cellular functions such as transcription, translation and DNA recombination. [Pg.3]

Figure 2.4 Noradrenergic inhibition of Ca " currents and transmitter release in sympathetic neurons and their processes, (a) Inhibition of currents through N-type Ca " channels by external application of noradrenaline (NA) or by over-expression of G-protein P y2 subunits, recorded from the soma and dendrite of a dissociated rat superior cervical sympathetic neuron. Currents were evoked by two successive 10 ms steps from —70 mV to OmV, separated by a prepulse to -1-90 mV. Note that the transient inhibition produced by NA (mediated by the G-protein Go) and the tonic inhibition produced by the G-protein Piy2 subunits were temporarily reversed by the -1-90 mV depolarisation. (Adapted from Fig. 4 in Delmas, P et al. (2000) Nat. Neurosci. 3 670-678. Reproduced with permission), (b) Inhibition of noradrenaline release from neurites of rat superior cervical sympathetic neurons by the 2-adrenoceptor stimulant UK-14,304, recorded amperometrically. Note that pretreatment with Pertussis toxin (PTX), which prevents coupling of the adrenoceptor to Gq, abolished inhibition. (Adapted from Fig. 3 in Koh, D-S and Hille, B (1997) Proc. Natl. Acad. Sci. USA 1506-1511. Reproduced with permission)... Figure 2.4 Noradrenergic inhibition of Ca " currents and transmitter release in sympathetic neurons and their processes, (a) Inhibition of currents through N-type Ca " channels by external application of noradrenaline (NA) or by over-expression of G-protein P y2 subunits, recorded from the soma and dendrite of a dissociated rat superior cervical sympathetic neuron. Currents were evoked by two successive 10 ms steps from —70 mV to OmV, separated by a prepulse to -1-90 mV. Note that the transient inhibition produced by NA (mediated by the G-protein Go) and the tonic inhibition produced by the G-protein Piy2 subunits were temporarily reversed by the -1-90 mV depolarisation. (Adapted from Fig. 4 in Delmas, P et al. (2000) Nat. Neurosci. 3 670-678. Reproduced with permission), (b) Inhibition of noradrenaline release from neurites of rat superior cervical sympathetic neurons by the 2-adrenoceptor stimulant UK-14,304, recorded amperometrically. Note that pretreatment with Pertussis toxin (PTX), which prevents coupling of the adrenoceptor to Gq, abolished inhibition. (Adapted from Fig. 3 in Koh, D-S and Hille, B (1997) Proc. Natl. Acad. Sci. USA 1506-1511. Reproduced with permission)...
Later steps after the adaptation output involve transient changes of cAMP levels and a mutant with a defect in the madD gene turned out to have an altered phosphodiesterase. This madD mutant is the first behavioral mutant of Phycomyces whose biochemical nature is known. [Pg.109]

Fig. 19. Sampled-current voltammogram constructed from the current-time transients that resulted from a series of potential-step experiments at a stationary Pt electrode in a 35.0 x 10 3 mol L-1 solution of Ni(II) in the 66.7 m/o AlCl3-EtMeImCl melt ( ) total current, ( ) partial current for the electrodeposition of Ni, (O) partial current for the electrodeposition of Al. The total current was sampled at 3 s after the application of each potential pulse. Adapted from Pitner et al. [47] by permission of The Electrochemical Society. [Pg.307]

The first laser Raman spectra were inherently time-resolved (although no dynamical processes were actually studied) by virtue of the pulsed excitation source (ruby laser) and the simultaneous detection of all Raman frequencies by photographic spectroscopy. The advent of the scanning double monochromator, while a great advance for c.w. spectroscopy, spelled the temporary end of time resolution in Raman spectroscopy. The time-resolved techniques began to be revitalized in 1968 when Bridoux and Delhaye (16) adapted television detectors (analogous to, but faster, more convenient, and more sensitive than, photographic film) to Raman spectroscopy. The advent of the resonance Raman effect provided the sensitivity required to detect the Raman spectra of intrinsically dilute, short-lived chemical species. The development of time-resolved resonance Raman (TR ) techniques (17) in our laboratories and by others (18) has led to the routine TR observation of nanosecond-lived transients (19) and isolated observations of picosecond-timescale events by TR (20-22). A specific example of a TR study will be discussed in a later section. [Pg.466]

Fig. 2.12. Left transient anisotropic reflectivity change of the (001) surface of single crystal type Ha diamond. Inset shows the FT spectrum of the oscillation, demonstrating a narrow peak of the optical phonon at 40THz. Right pump and probe polarizations to detect the optical phonon. Adapted from [50]... Fig. 2.12. Left transient anisotropic reflectivity change of the (001) surface of single crystal type Ha diamond. Inset shows the FT spectrum of the oscillation, demonstrating a narrow peak of the optical phonon at 40THz. Right pump and probe polarizations to detect the optical phonon. Adapted from [50]...
Fig. 3.14. Left transient reflectivity change of Te obtained with transform limited, negatively chirped, and positively chirped pulses. Right coherent phonon amplitude as a function of the pulse chirp. Adapted from [42]... Fig. 3.14. Left transient reflectivity change of Te obtained with transform limited, negatively chirped, and positively chirped pulses. Right coherent phonon amplitude as a function of the pulse chirp. Adapted from [42]...
Figure 5.17 Superoxo transient formed in oxygenation reactions of [Cu (N4)]2+. (Adapted from Scheme 2 of Karlin, K. D. Kaderli, S. Zuberbiihler, A. D. Acc. Chem. Res., 1997, 30, 139-147. Copyright 1997, American Chemical Society.)... Figure 5.17 Superoxo transient formed in oxygenation reactions of [Cu (N4)]2+. (Adapted from Scheme 2 of Karlin, K. D. Kaderli, S. Zuberbiihler, A. D. Acc. Chem. Res., 1997, 30, 139-147. Copyright 1997, American Chemical Society.)...
Although separate determination of the kinetic and thermodynamic parameters of electron transfer to transient radicals is certainly important from a fundamental point of view, the cyclic voltammetric determination of the reduction potentials and dimerization parameters may be useful to devise preparative-scale strategies. In preparative-scale electrolysis (Section 2.3) these parameters are the same as in cyclic voltammetry after replacement in equations (2.39) and (2.40) of Fv/IZT by D/52. For example, a diffusion layer thickness S = 5 x 10-2 cm is equivalent to v = 0.01 V/s. The parameters thus adapted, with no necessity of separating the kinetic and thermodynamic parameters of electron transfer, may thus be used to defined optimized preparative-scale strategies according to the principles defined and illustrated in Section 2.4. [Pg.171]

Voluntary muscles contain a variety of fibre types which are specialized for particular tasks. Most muscles contain a mixture of fibre types although one type may predominate. All human skeletal muscles are composed of several different muscle fibre types. Up to seven different fibre types have been identified histochemically based on the pH stability of myofibrillar adenosine triphosphatase and on the myosin heavy chain profile. Innumerable fibre type transients exist due to continuing adaptation processes. However, three main... [Pg.7]


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See also in sourсe #XX -- [ Pg.68 ]




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