Bell violations with alternative transformations
Classical particles and classical waves display the same non-linear patterns of energy redistribution. However, these transformations are governed by system-level interactions, with an interesting caveat. In the case of billiard ball collisions, a single ball represents a full macroscopic system. It is able to transfer kinetic energy according to non-linear rules, but we cannot meaningfully “quantize” the motion of a billiard ball into detectable increments. In contrast, optical projections have a natural correspondence between macroscopic energy redistribution and microscopic single-event distributions. After all, wave energy is proportional to the amplitude squared, which is also proportional to the number of quanta in the same projection:
At the quantum level, we use system-level predictions, captured by wave-functions, to predict the probability of detecting single events, also by squaring relevant amplitudes with Born’s rule:
Hence, there is a natural way to convert system-level energy redistribution into expectation values for various patterns of coincidence at the individual level. For a CHSH experiment, the task is simply to identify a rotationally invariant pattern of energy redistribution, which can be achieved with depolarized optical projections. Yet, this phenomenon is already associated with non-physical interpretations that hinder the analysis of quantum correlations. Is it possible to find a classical system that can better elucidate the local nature of Bell violations?
Consider a flexible fluid-splitter, as shown in
Figure 3A. The vertical pipe feeds some kind of fluid into a flexible T-junction with two output pipes leading in opposite directions. The input pipe is rigid in the
z-direction, while the output axis can be rotated at will in the
x-y plane. Fluid is pumped into this system under pressure and is split 50-50. For example, half of the fluid could be directed into the “plus”
y-direction and the other half into the “minus”
y-direction. Though, imagine that we freeze the process, and ask a counterfactual question. How much fluid from the “plus” output would have been in the same pipe, if the axis of the splitter was rotated in the
x-y plane by an arbitrary angle? To answer this question, we need to assume that fluid splitting is a fundamentally deterministic process. It is not an accident that the molecules from the “plus” output are found in this channel. Ergo, if the same exact process were to be replayed again, the same exact molecules of fluid would be found in the same output. That being said, we are not dealing with independent ballistic particle trajectories. The motion of fluid molecules is inseparable from the motion of the fluid as a whole. The question is: how does the fluid, as a macroscopic system, interact with the walls of the flexible fluid splitter?
A plausible assumption in this scenario is that a reference output direction “
a+” is associated with a conserved amount of kinetic energy carried by the fluid. Furthermore, transverse redistribution of kinetic energy into some new orientation “
b+” is known to follow a cosine squared law:
If a given sliver of fluid has a fixed amount of kinetic energy in the
a+ direction, then it can only impart a fraction in the
b+ direction, determined by the cosine squared of half the angle between the two orientations. The other amount of kinetic energy, to maintain rotational invariance, must come from the opposite (
a-) direction. Yet, notice that the magnitude of fluid velocity does not change under transverse redirection in the fluid splitter. The fluid pressure inside the pipes remains constant. Therefore, the cosine squared law must be physically satisfied by a non-linear redistribution of
fluid mass between alternative directions. The mass of the fluid in any new direction
b+ must be composed of cosine-squared of half the angle from the mass that was emitted in the
a+ direction, plus a supplementary amount from the
a- direction:
Assuming uniform fluid density, it follows that the probability of any fluid molecule to display correlated behavior between two alternative orientations is also non-linear:
In other words, the proportion of fluid molecules that can also emerge in the “plus” channel for direction b given that they emerged in the “plus” channel for direction a, is determined by the cosine squared of half the angle between the two directions. This translates into corresponding probabilities at the level of single molecules. For example, if the output axis was shifted by 45˚ relative to the y-axis, then 85% of the water molecules would have been the same in the “plus” channel, while 15% would have traded places with the “minus” channel. On the one hand, we have a system-level effect that is observable as fluid motion. On the other hand, we have molecular behavior expressing the non-linear features of this macroscopic process.
The offshoot of this description is that we have rotationally invariant correlations between any two output settings for the fluid-splitter. It does not matter which axis is chosen for reference and which transformation is added for correlation analysis. One way or another, 50% of the input fluid would end up in the “plus” channel. For any other output orientation, the proportion of the molecules that would have been in the same channel (and the supplementary proportion that trade places) are determined by the cosine squared of half the angle between the two settings. This means that we can choose several adjacent orientations, separated by 45˚ angles, as shown in
Figure 3B. To keep the analogy with a CHSH quantum experiment [
26], we can label these directions as
a1,
b1,
a2 and
b2. Just as described above, we can ask: what proportion of molecules would have been correlated for any of the possible pairwise combinations? The answer is that three combinations are separated by 45˚, with a final coefficient of correlation of:
In contrast, the last combination spans an angle of 135˚. Therefore,
We can plug these four expectation values into the CHSH expression for a Bell test with four variables [
26]:
As a result, we obtained a Tsirelson violation of the CHSH inequality [
27], just as predicted for quantum correlations between two entangled electron beams. However, we derived this behavior for alternative orientations of a
single classical fluid splitter. This was done deliberately, to clarify the local nature of these correlations. All the settings of a Bell experiment with photon polarization or electron spin correspond to various incompatible transformations that can happen in one and the same system, locally. They just happen to obey nonlinear rules.
Of course, it is not possible to observe the same exact molecules in two different scenarios in one step. This was an exercise in counterfactual analysis, as if we had the ability to replay the same physical process in different alternative ways. However, it is possible to simulate the behavior of a fluid with molecular level precision in a modern computer. Furthermore, it is possible for two different computers to play back the same simulation from the source to the flexible neck of the fluid splitter. In this case, one computer named Alice can choose between two output settings (such as 0˚or 90˚, relative to the y-axis), while another computer named Bob can choose between two other settings (such 45˚ and 135˚, relative to the y-axis). The settings for both Alice and Bob can be chosen at random, or supplied by a third party, or even pre-arranged in advance. It does not matter how the settings are chosen, since – in the end – only four combinations are possible, as explained above. (This is an important conclusion, given that “freedom of choice” is an essential requirement for loophole-free Bell experiments). The correlations between these settings are rotationally invariant and obey the cosine squared law. Yet, this law does not describe non-local effects between the measurements of Alice and Bob. As shown above, these are natural types of behavior that can happen locally in each system, during binary energy redistribution. Similarly, Alice and Bob could be making coincidence studies with identically stacked decks of playing cards. In both cases, the correlations would be local. The difference is that the properties of playing cards are jointly distributed and cannot violate Bell-type inequalities.
This thought experiment can even be extended to “single event” detection schemes. For example, it is possible to inject die molecules into the fluid, one at a time, and to observe their fate at the output: do they emerge in the “plus” or “minus” output pipe for any chosen setting? The behavior of die molecules would also be inseparable from the behavior of the fluid as a whole. Therefore, their output statistics, and the corresponding correlations between Alice-Bob simulations, are expected to display the same patterns as described above. Upon closer inspection, this is not very different from quantum behavior, where individual-level statistics are governed by system-level (quasi-macroscopic) effects, as captured formally by quantum wave-functions. By implication, quantum behavior is also local.