(1) n(θ) = cos2(θ) ,
where θ is the angle between the two polarizers and n(θ) the relative coincidence count rate.(2) E(x,y,t) = Ex(t).ex + Ey(t).ey
where ex and ey are the unit vectors in the x and y direction respectively. Ex(t) and Ey(t) are the electric field fluctuations along these axes. These are in general not sinusoidal but, due to the superposition of the emissions of many (uncorrelated) atoms, stochastic functions of time which can only technically be described as a coherent wave on time scales shorter than the coherence length of the atomic emissions (see https://www.plasmaphysics.org.uk/research/coherence.htm for a corresponding numerical simulation); the exact form of the time dependence is however irrelevant as even for separated 'single photons' the 'global' time dependence over the time required to emit the photoelectron will be different for different polarisation directions due to the different amplitudes (the only requirement for this is the condition that the coherence time of the radiation field is shorter than the time required for photoionization, which is easily the case considering typical single detector count rates of about 104/sec)). Projecting now E(x,y,t) on a given direction of polarization(3) P(x,y,θ) = cos(θ).ex + sin(θ).ey
yields(4) Ep(t) = E(x,y,t).P(x,y,θ) = Ex(t).cos(θ) + Ey(t).sin(θ) .
If one defines the coordinate system such that the x-axis coincides with the direction of the polarizer of detector 1 (i.e. θ=0) , the projection of the radiation field onto the orbital plane of an atomic electron i (with inclination αi) in detector 1 is therefore(5) E1,i(0,t) = Ex(t).cos(αi) .
and the projection onto the orbital plane of an atomic electron j in detector 2 (with the polarizer rotated by a relative angle θ) is(6) E2,j(θ,t) = [ Ex(t).cos(θ) + Ey(t).sin(θ) ].cos(αj-θ) ,
which using the addition theorem for trigonometric functions yields
(7) E2,j(θ,t) = Ex(t). [cos2(θ).cos(αj) + cos(θ).sin(θ).sin(αj)]
+ Ey(t).[sin2(θ).sin(αj) + cos(θ).sin(θ) .cos(αj)] .
(8) <f(t).g(t)> := 1/T . 0∫Tdt f(t).g(t) ,
where T is a sufficiently long integration time.
(9) <E1,i(0,t).E2,j(θ,t)> = cos(αi).[ cos2(θ).cos(αj) + cos(θ).sin(θ).sin(αj)] .<Ex(t). Ex(t)>
+ cos(αi).[sin2(θ).sin(αj) + cos(θ) .sin(θ).cos(αj)] .<Ex(t). Ey(t)> .
(10) Ex(t) = E(t).cos(φ(t))
(11) Ey(t) = E(t).sin(φ(t)) ,
(12) <Ex(t).Ey(t)>= 1/T . 0∫Tdt E2(t).cos(φ(t)).sin(φ(t)) = 0 for T→∞
as the integrand oscillates between positive and negative values (unless the radiation is linearly polarized i.e. φ(t)=const.) and can thus at best grow proportional to √T (if φ(t) is a stochastic function) i.e. the normalized integral will tend to zero for growing T in case of overall unpolarized radiation. If we now furthermore normalize Eq.(9) to the cross correlation for parallel polarizers(13) <E1,i(0,t).E2,j(0,t)> = cos(αi).cos(αj). <Ex(t). Ex(t)> ,
we obtain thus(14) nj(θ) := <E1,i(0,t). E2,j(θ,t)>/<E1,i(0,t). E2,j(0,t)> = cos2(θ) + cos(θ).sin(θ).tan(αj) .
If we now perform an ensemble average over all atomic electrons j, the second term vanishes for an isotropic distribution of αj and hence we have(15) n(θ) = cos2(θ)
i.e. the relative cross-correlation (and thus the coincidence probability) is distributed according to Malus' law Note: The assumption of identical functions Ex(t) and Ey(t) at both detectors would strictly speaking imply that both the frequencies and decay times of the two correlated radiative emissions are identical, which is in general not the case. On the other hand, we are of course not actually interested in exact correlations (as implied by Eq.(8)) but only ones that occur within a certain 'coincidence window'. With a correspondingly generalized treatment one should thus expect an identical result to the present one as long as there is some correlation at all, because only the components of the two beams which are polarized along the same direction have maximum correlation as all atomic emissions are reduced by exactly the same amount by both polarizers. If the polarizers point into different directions however, this is not the case anymore and the correlation is lost. As the Bell test experiments can in this way be explained on a classical basis, they do therefore not introduce any new aspects into physics and in particular do not invalidate the objective physical reality of the polarization of radiation (and consequently neither lead to the conclusion of the existence of a non-local entanglement). Even with the present interpretation, some people may be tempted to again interprete the Malus law as an instantaneous non-local interaction occuring, but it should be obvious from the above treatment that the Malus law is actually only a consequence of the fact that a) the radiation field is a continuous stochastic function of time producing photoionization events in the detectors at certain times and b) that this function is completely uncorrelated for orthogonal directions of polarization. This means that in the latter case no coincidences (apart from accidental ones) are detected. However, this reflects only the nature of the original radiation fields, but does not imply any causal connection between the polarization- or detection processes.