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This is a correction to Theorems 7.3 and 8.12 in [1]. These statements claimed to deduce the spatial Plancherel formula (spatial biorthogonality) of the ASEP and XXZ eigenfunctions from the corresponding statements for the eigenfunctions of the q-Hahn system. Such a reduction is wrong. We are grateful to Yier Lin for pointing this out to us.
We have updated the arXiv version of the paper with the necessary corrections [2]. Below is the summary of the issue and the steps we made to correct the presentation of the ASEP and XXZ applications of our results about the q-Hahn eigenfunctions.
1 q-Hahn Spatial Biorthogonality
Recall that the q-Hahn left and right eigenfunctions are given by
where \(\vec n=(n_1\ge \cdots \ge n_k )\). (Here and below we bring only the essential notation from the original paper [1].) Their spatial biorthogonality written in the small contour form reads [1, Corollary 3.13]
with all integration contours being small positively oriented circles around 1, and where
Here, \({\vec w}=(w_1,\ldots ,w_{\ell (\lambda )})\in \mathbb {C}^{\ell (\lambda )}\), and \(m_j\) is the number of components of \(\lambda \) equal to j (so that \(\lambda =1^{m_1}2^{m_2}\ldots \)), and
2 ASEP Spatial Biorthogonality
To obtain the ASEP eigenfunctions from the q-Hahn ones, we set \(\nu =1/q=1/\tau \), where \(\tau \in (0,1)\) is the ASEP asymmetry parameter:
Here, \(x_1<\cdots <x_k \) are the ASEP spatial coordinates. The spatial biorthogonality of the ASEP eigenfunctions reads
where the integration is performed over sufficiently small positively oriented circles around \(-1\). This biorthogonality of the ASEP eigenfunctions follows from the paper by Tracy and Widom [4], as we explain in detail in [2, Proof of Theorem 7.3]. Next we discuss the gap in our original argument.
3 Why (2) Does Not Follow from (1) as Claimed
The “proof” of ASEP spatial biorthogonality given in [1] claimed to deduce (2) by plugging \(\nu =1/q\) into (1) before performing the integration. Indeed, identity (2) looks as if one takes the q-Hahn small contour formula (1), removes all terms corresponding to partitions \(\lambda \ne (1^k)\), and then plugs in \(\nu =1/q\), \(q=\tau \). Formula (2) (following from [4]) a posteriori implies that under this specialization, the contribution of all additional terms with \(\lambda \ne (1^k)\) vanishes.
First, observe that the substitution \(\nu =1/q\) before the integration might change the value of the integral because of the factors of the form \(\frac{1}{1-q \nu w_i}\) in the integrand for \(\lambda \ne (1^k)\). Before the substitution \(\nu =1/q\), the residue at \(w_i=(q \nu )^{-1}\) was not picked while after the substitution we have \(1-q \nu w_i=1-w_i\), so this factor adds an extra pole inside the integration contour.
With the agreement that the substitution \(\nu =1/q\) occurs after the integration, the “proof” of (2) presented in [1] asserted a stronger statement: For each individual \(\lambda \ne (1^k)\) and any two permutations \(\sigma , \omega \in S(k)\) (coming from \(\Psi _{\vec z}^\ell \) and \(\Psi _{\vec z}^{r}\), respectively), the corresponding term vanishes after setting \(\nu =1/q\). This assertion is wrong.
For example, take \(\vec x=(10,9,8,7,6,5)\) and \(\vec y=(5,4,3,2,1,0)\). The summand in the integrand in (1) corresponding to \(\lambda =(3,2,1)\), and permutations \(\sigma =321{,}546\) and \(\omega =645{,}123\) has the form (before setting \(q=1/\nu =\tau \)):
Here, \(f_1(w_1)\) is independent of \(w_2,w_3\) and has no zeroes or poles at \(w_1=1\) and \(w_1=1/(q\nu )\), and similarly for \(f_2(w_2)\) and \(f_3(w_3)\). One can check that the residue of this term at \(w_3=1\), \(w_2=1\), and \(w_1=1\) does not vanish when setting \(q=1/\nu \). (Note that the result of the integration depends on the order of taking the residues for individual summands due to the presence of the factors of the form \(w_i-w_j\) in the denominators. These factors cancel out after summing over all permutations \(\sigma ,\omega \), and each summand indexed by \(\lambda \) is independent of the order of integration because the result of the summation is a function symmetric in the \(w_i\)’s.)
Let us mention another (possibly related) subtlety in the spatial biorthogonality of the ASEP eigenfunctions as compared to the general q-Hahn case. Namely, in the q-Hahn situation the contribution of individual permutations coming from the eigenfunctions vanishes, while in the ASEP case this is not the case (see [2, Remark 7.6] for details). The proof of the ASEP statement in [4] employs nontrivial combinatorics to determine cancellations of specific combinations of permutations.
4 Corrections We Made in the New Version [2] Compared to the Published Version [1]
We have replaced the incorrect “proof” of Theorem 7.3 (spatial biorthogonality of the ASEP eigenfunctions) by its derivation from the earlier result of Tracy and Widom [4]. We have also removed Theorem 8.12 which claimed a spatial biorthogonality statement of the XXZ eigenfunctions based on a similar incorrect direct substitution \(\nu ={\varvec{\theta }}\).
5 The Same Gap in [3]
The claim similar to (1) but with more general \(\nu =q^{-I}\), where I is an arbitrary positive integer, is made in [3, Appendix A] (by a subset of the current authors). When \(I=1\), this identity is correct, but does not follow from the general \(\nu \in (0,1)\) formulas (as explained above). Moreover, for \(I\ge 2\) the claimed orthogonality does not seem to hold as stated. A separate erratum will be prepared to address the issues in the work [3].
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Borodin, A., Corwin, I., Petrov, L. et al. Correction to: Spectral Theory for Interacting Particle Systems Solvable by Coordinate Bethe Ansatz. Commun. Math. Phys. 370, 1069–1072 (2019). https://doi.org/10.1007/s00220-019-03528-y
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DOI: https://doi.org/10.1007/s00220-019-03528-y