vanesch
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I only skimmed through the article, but I think Kirkpatrick is somehow wrong when attacking Hughes' argument (with which I think I'm familiar) on top of p 2, because I think this argument is correct.Bertrand said:Hi,
Being new to this forum, I'm not sure this is the right place to ask my question. I had no time to read all the posts of this very interesting debate, and maybe this subject was already addressed somewhere...
My question is :
B. D'Espagnat states that the reduced density matrix of a subsystem A of a composite system "A+B", obtained through the partial trace operation on B, doesn't necessarily represent a mixture, but what he calls an "improper mixture".
in the following article :
http://arxiv.org/PS_cache/quant-ph/pdf/0109/0109146.pdf
the author, K.A. Kirkpatrick shows that D'Espagnat is wrong somewhere in his reasoning, and that, therefore, this reduced matrix may indeed be considered as representing a "true mixture".
Kirkpatrick's argument is based on indistinguishability, but I don't really get it.
Could someone explain it ? My last question is, finally, who is right and who is wrong ?
Thanks for help,
Bertrand
There's a difference between having independent statistics for the systems S and M, given by the two reduced density matrices, and the correlated statistics that will result when applied to the pure state. However, this correlation will not show, of course, if all measurements are of the form A_S x 1 or 1 x B_M (in other words, when we do not measure correlations between S and M, but do independent measurements on S alone, or on M alone), at least, in the case when the systems S and M are entangled (that means, that the pure state is not a product state). If the systems S and M are not entangled, then the individual reduced density matrices will also give rise to individual pure states. The only case in which the reduced density matrix is not pure, while the "master" state is pure, is when the system is entangled.
So the point of Hughes (which I think is correct), is that he physical state of a global system (S + M) in a pure state is not correctly described by only the mixtures given by the reduced density matrices. These only give the correct result for measurements who do not try to establish correlations between the systems S and M. Only the pure state gives the right correlations, while the local density matrices assume statistical independence and hence erroneous results for these correlations.Kirkpatrick might be right, however, that in absense of explicit projection, there's no such thing as a proper mixture if we didn't start with one. But that's known: it is the entire issue of the measurement problem: how to produce a genuine mixture, by unitary evolution, from a pure state (which doesn't work).
Simple example:
|psi> = a |+> |-> + b |->|+>
This gives, for the first system, a reduced density matrix as mixture:
a^2 |+><+| + b^2 |-><-|
and for the second system:
b^2 |+><+| + a^2 |-><-|
But an overall operator measuring the state:
a |+>|-> + b|->|+> ==> outcome 1
all other orthogonal states ==> outcome 0
would give expectation value = 1 when applied to the pure state,
and an expectation value below 1 when applied assuming statistical
independence.
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