Correlation theorem

According to the correlation theorem (Press et ah, 1987, p. 383), the inverse Fourier transform of the product of spectrum of one function and the complex conjugate spectrum of another function is equal to correlation of these functions. Therefore, we can write the numerator in formula (15.38) as a cross correlation of the time derivatives of the back-propagated scattered field and the incident wavefield ... 

Equation (4.3.5) is the Fourier transform of the linear correlation (4.3.1). This relationship is referred to as the correlation theorem. If x(t) is white noise, then ensemble averages have to be incorporated into equations (4.3.5)-(4.3.7), because the power spectrum of white noise is again white noise, but with a variance as large as its mean value [Beni]. When the linear correlation theorem (4.3.5) is applied to the same functions, then Ci((o) is the power spectrum of Y((o) = X co). Conversely, Ci(w) is then the Fourier transform of the auto-correlation function of y(f) = x(t) (cf. eqn 4.3.1). 

Numerical execution of cross-correlations on a conventional computer is demanding in time. The processing time could be significantly reduced by use of dedicated processors for parallel computing, but computation in the time domain can be avoided altogether if time-invariant field gradients are employed. Projections of the spin density are obtained by Fourier transformation of the ID (4.3.2) and 3D (eqn (4.3.3) with n—y) cross-correlation functions. With the correlation theorem (cf. Section 4.3.3),... 

Correlation theorem, 121 Correspondence theorem, Bohr, 8 Cosets, 87, 123. 350... 

The Correlation Theorem. A remarkable theorem can be proved concerning the number of times, a given species y will occur in the reduction of the representation generated by a complete equivalent set of coordinates. Si, Si,. . . , Si,. . . . The operations of the complete point group g which are such that... 

The convolution and correlation theorems allow us to determine those functions using Fourier methods instead of direct integration. Before we discuss the two topics further, we choose to write all the key formulas here - in one place - so we can compare them easily. 

Correlation using Fourier Methods - The Correlation Theorem... 

This process applies to all convolution problems, including the effect of a lens when imaging a target, and the effect of an electrical circuit on an input waveform. Remember that we do not do any reversals when doing the integration directly - it is only when applying the Correlation Theorem that we must create a reversed-x ... 

The response fiinction H, which is defined in equation (A3.3.4), is related to the corresponding correlation fiinction, kliroiigh the fluctuation dissipation theorem ... 

The fluctuation dissipation theorem relates the dissipative part of the response fiinction (x") to the correlation of fluctuations (A, for any system in themial equilibrium. The left-hand side describes the dissipative behaviour of a many-body system all or part of the work done by the external forces is irreversibly distributed mto the infinitely many degrees of freedom of the themial system. The correlation fiinction on the right-hand side describes the maimer m which a fluctuation arising spontaneously in a system in themial equilibrium, even in the absence of external forces, may dissipate in time. In the classical limit, the fluctuation dissipation theorem becomes / /., w) = w). 

A Hbasis functions provides K molecular orbitals, but lUJiW of these will not be occupied by smy electrons they are the virtual spin orbitals. If u c were to add an electron to one of these virtual orbitals then this should provide a means of calculating the electron affinity of the system. Electron affinities predicted by Konpman s theorem are always positive when Hartree-Fock calculations are used, because fhe irtucil orbitals always have a positive energy. However, it is observed experimentally that many neutral molecules will accept an electron to form a stable anion and so have negative electron affinities. This can be understood if one realises that electron correlation uDiild be expected to add to the error due to the frozen orbital approximation, rather ihan to counteract it as for ionisation potentials. 

The volumetric properties of fluids are represented not only by equations of state but also by generalized correlations. The most popular generalized correlations are based on a three-parameter theorem of corresponding states which asserts that the compressibiHty factor is a universal function of reduced temperature, reduced pressure, and a parameter CO, called the acentric factor ... 

In spite of its simplicity and the visual similarity of this equation to Eq. (7), we would like to note that Eq. (11) leads to a nontrivial thermodynamics of a partially quenched system in terms of correlation functions, see, e.g.. Ref. 25 for detailed discussion. Evidently, the principal route for and to the virial theorem is to exploit the thermodynamics of the replicated system. However, special care must be taken then, because the V and s derivatives do not commute. Moreover, the presence of two different temperatures, Pq and P, requires attention in taking temperature derivatives, setting those temperatures equal, if appropriate, only at the end of the calculations. 

In standard quantum-mechanical molecular structure calculations, we normally work with a set of nuclear-centred atomic orbitals Xi< Xi CTOs are a good choice for the if only because of the ease of integral evaluation. Procedures such as HF-LCAO then express the molecular electronic wavefunction in terms of these basis functions and at first sight the resulting HF-LCAO orbitals are delocalized over regions of molecules. It is often thought desirable to have a simple ab initio method that can correlate with chemical concepts such as bonds, lone pairs and inner shells. A theorem due to Fock (1930) enables one to transform the HF-LCAOs into localized orbitals that often have the desired spatial properties. 

It is a well known fact, called the Wiener-Khintchine Theorem [gardi85], that the correlation function and power spectrum are Fourier Transforms of one another ... 

The second axiom, which is reminiscent of Mach s principle, also contains the seeds of Leibniz s Monads [reschQl]. All is process. That is to say, there is no thing in the universe. Things, objects, entities, are abstractions of what is relatively constant from a process of movement and transformation. They are like the shapes that children like to see in the clouds. The Einstein-Podolsky-Rosen correlations (see section 12.7.1) remind us that what we empirically accept as fundamental particles - electrons, atoms, molecules, etc. - actually never exist in total isolation. Moreover, recalling von Neumann s uniqueness theorem for canonical commutation relations (which asserts that for locally compact phase spaces all Hilbert-space representations of the canonical commutation relations are physically equivalent), we note that for systems with non-locally-compact phase spaces, the uniqueness theorem fails, and therefore there must be infinitely many physically inequivalent and... 

Any changes in the potential energy because of the Coulomb correlation must therefore also influence the kinetic energy. The virial theorem will be further discussed below. 

We note that the virial theorem is automatically fulfilled in the Hartree-Fock approximation. This result follows from the fact that the single Slater determinant (Eq. 11.38) built up from the Hartree-Fock functions pk x) satisfying Eq. 11.46 is the optimum wave function of this particular form, and, since this wave function cannot be further improved by scaling, the virial theorem must be fulfilled from the very beginning. If we consider a stationary state with the nuclei in their equilibrium positions, we have particularly Thf = — Fhf, and for the correlation terms follows consequently that... 

The results show that it is possible to improve the Hartree-Fock energy —2.86167 at.u. considerably by means of a simple correlation factor, but also that it is essential to scale the total function W properly to fulfil the virial theorem. The parameters in the best function u of the form of Eq. III. 121 are further given below ... 

Using the summation theorem for spherical harmonics, these correlation functions may be represented as scalar products... 

Using the impact approximation presented in Chapter 6, they may easily be found for any rotational band even if rotational-vibrational interaction is nonlinear in J. In 1954 R W. Anderson proved as a theorem [104] that expansion of the spectral wings in inverse powers of frequency is controlled by successive odd derivatives of the correlation function at the origin. In impact approximation the lowest non-zero derivative of this type is the third and therefore asymptotics G/(co) is described by the power expansion [20]... 

We are now ready to derive an expression for the intensity pattern observed with the Young s interferometer. The correlation term is replaced by the complex coherence factor transported to the interferometer from the source, and which contains the baseline B = xi — X2. Exactly this term quantifies the contrast of the interference fringes. Upon closer inspection it becomes apparent that the complex coherence factor contains the two-dimensional Fourier transform of the apparent source distribution I(1 ) taken at a spatial frequency s = B/A (with units line pairs per radian ). The notion that the fringe contrast in an interferometer is determined by the Fourier transform of the source intensity distribution is the essence of the theorem of van Cittert - Zemike. 

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