Abstract
Assume that each species l has its own jump rate in the multi-species totally asymmetric simple exclusion process. We show that this model is integrable in the sense that the Bethe ansatz method is applicable to obtain the transition probabilities for all possible N-particle systems with up to N different species.
1. Introduction
The multi-species asymmetric simple exclusion process on is a generalization of the asymmetric simple exclusion process (ASEP) on in the sense that each particle may belong to a different species labelled by an integer . Each particle jumps to the right by one step with the probability p or to the left by one step with the probability after a waiting time that is exponentially distributed with rate 1. If a particle belonging to l attempts to jump to the site occupied by a particle belonging to , the jump is prohibited; however, if a particle belonging to attempts to jump to the site occupied by a particle belonging to , then the jump occurs by interchanging positions.
The transition probabilities and some determinantal formulas for the multi-species ASEP and its special cases were found in [,,,,]. For certain special initial conditions with a single second class particle, some distributions and their asymptotics were studied in [,]. More recently, asymptotic behaviors of the second class particles were studied using the color-position symmetry, see []. In fact, the multi-species asymmetric simple exclusion process can be considered in a more general context—that is, the coloured six vertex model [].
Another direction of generalizing the ASEP and other models studied in the integrable probability is to make the jump rates inhomogeneous. It is known that the Bethe ansatz method is still applicable to some single-species model with inhomogeneous jump rates. The basic idea of using the Bethe ansatz in the ASEP is that the generator of the ASEP is a similarity transformation of the XXZ quantum spin system. Considering that the Bethe ansatz is a method to find eigenvalues and eigenvectors of a certain class of quantum spin systems, we use the Bethe ansatz to find the solution of the forward equation of a certain class of Markov processes, that is, the transition probabilities of the processes.
Of course, for some particle models, the Bethe ansatz method cannot be used. For the background of Bethe ansatz, see [,]. It is known that the Bethe ansatz is applicable to some generalization of the ASEP. For example, the transition probability and the current distribution of the totally asymmetric simple exclusion process (TASEP) with particle-dependent rates were studied in [], and the transition probabilities and some asymptotic results for the q-deformed totally asymmetric zero range process with site-dependent rates were studied in [,].
In this paper, we consider the multi-species totally asymmetric simple exclusion processes with N particles in which particles move to the right and each species l is allowed to have its own rate . Following the notations used in [], let with represent the positions of particles, and let be a permutation of a multi-set with elements taken from and representing the species of the leftmost particle. Then, the state of an N-particle system is denoted by
Let us write for the transition probability from at to at a later time t. For fixed X and Y, is regarded as a matrix element of an matrix denoted by whose columns and rows are labelled by , respectively. Throughout this paper, given an matrix, we assume that its rows () and columns () are labelled by and that these labels are listed lexicographically, unless stated otherwise. The main result of this paper is that the multi-species TASEP with species-dependent rates is an integrable model, and we provide a formula analogous to (2.12) in [] using the Bethe ansatz method.
Statement of the Results
We first introduce a few objects to state the main theorem. Define an matrix with
where
Remark 1.
The form of the matrix (1) was obtained by induction via similar arguments to Sections 2.1 and 2.2 in [], which treats a special case, and the motivation of (2) is given in Section 2.1. Finding the form of (1) with (2) is the key idea of this paper.
Let be the simple transposition that interchanges the number at the th slot and the number at the st slot. If maps a permutation to , we write when necessary. Corresponding to a simple transposition , we define matrix by the tensor product of matrices,
where is the identity matrix. For a permutation in the symmetric group written
for some , we define
Here, is well defined, that is, is unique regardless of the representation of by simple transpositions. This well-definedness is due to the following lemma.
Lemma 1.
The following consistency relations are satisfied.
- (a)
- (b)
- (c)
The relations in Lemma 1 with for all l are already known for the multi-species ASEP.
Remark 2.
The definitions of and are motivated by the arguments for in Sections 2.1 and 2.2 in [], which treats a special case.
Let be the diagonal matrix whose -element is given by where
let be the diagonal matrix whose -element is given by , and let be the diagonal matrix whose -element is given by where s are the initial positions. In the next theorem, the integral of a matrix implies that the integral is taken element-wise, and ⨍ implies .
Theorem 1.
Let be given as in (5) and c be a positively oriented circle centred at the origin with a radius less than bl for all l in the complex plane . Then, the matrix of the transition probabilities of the multi-species TASEP with species-dependent rates is
Remark 3.
If , in other words, all N particles belong to different species, and the species are initially arranged in ascending order, then the system is the same as the TASEP with particle-dependent rates studied in []. Hence, the transition probability can be expressed as a determinant (see Theorem 1 in []).
Remark 4.
Theorem 1 partially extends (2.12) in []. In other words, (6) with is equal to (2.12) in [] with .
The proofs of Lemma 1 and Theorem 1 are given in the next section.
2. Proof of Theorem 1
In order to prove that the -element of the right-hand side of (6) is , we should show that the -element satisfies its forward equation and the initial condition .
2.1. Forward Equations
We first study the two-particle systems, which will be building-blocks for the formulas for N-particle systems. When , the forward equations of are straightforward because two particles act as free particles. Hence, the forward equations of are expressed as
where the derivative of the matrix on the left-hand side implies the matrix of the derivatives of elements of . The matrices and account for the probability current in the states by a particle’s jump to the right next site, which is empty. On the other hand, when , if two particles belong to different species, two particles may swap their positions. For example, if the initial state is , the system cannot be at at any later time t. Hence, the forward equation of is
On the other hand, for all t, because the model is totally asymmetric. If the initial state is , the forward equation of is
and the forward equation of is
Hence, the forward equations of are expressed as
Here, the matrix accounts for probability current going in the states by the species-2 particle’s jump from the state . Similarly, the matrix accounts for probability current going out of the states by species-2 particle’s jump to the state . Equations (7) and (8) imply that, if is a matrix whose elements are functions on , then the forward equation of for any is in the form of the -element of
subject to the -element of
Now, we extend the argument for two-particle systems to N-particle systems. The matrices and in (7) for two-particle systems are generalized to
where is the diagonal matrix,
The matrix in (8) is generalized to an matrix with
and let
The matrix in (8) is generalized to matrix with
and let
All forward equations of may be expressed as a matrix equation. For example, if for all i, then the forward equation of is the -element of
and if and for all ,
For other configurations of , the form of the matrix of the forward equations may be different from (9) and (10). However, as in other Bethe ansatz applicable models, if is an matrix whose elements are functions on , then the forward equation of for any is in the form of the -element of
subject to the -element of
for all .
2.2. Solutions of the Forward Equations via Bethe Ansatz
The -element of (11) is
Assume the separation of variables to write . Then, the equation of the spatial variables is
for some constant with respect to . Then, we observe that, for any ,
solves (13) if and only if
Based on the observation in the above, assume that the matrix is invertible and that it is decomposed as
where is an diagonal matrix where are functions of time only. Hence, from (11), we obtain
Both sides of (15) must be a diagonal matrix whose elements are some constants with respect to . Thus, we obtain the matrix equation for spatial variables
and the matrix equation for the time variable
Lemma 2.
Let be an diagonal matrix with
Then, for any ,
where is an arbitrary invertible matrix whose elements are constants with respect to is a solution of (16) if and only if is given by
Proof.
First, we observe that
because is a diagonal matrix whose -element is . We observe that
and
Now, we prove the statement. Suppose that (17) is a solution of (16). Substituting (17) into (16) and then dividing both sides by , then
Multiplying by on both sides, we obtain
and thus, the -element of is given by (18). The second part of the proof can be done via the reverse way of the first part of the proof. □
The previous lemma implies that the general solution of (16) is given by
2.3. Boundary Conditions
Now, (19) should satisfy the spatial part of the boundary condition (12), that is,
for . Extending the technique used in [], we will find the formulas of in (19), which satisfy (20). Define an diagonal matrix,
and recall the definition of in (1). Then, we observe that
Lemma 3.
If
for all even permutations σ and , then (20) is satisfied.
Proof.
First, we note that
and
Substituting (19) into (20), we obtain
If we express (22) as a sum over the alternating group
However, (23) is satisfied if
for each even permutation , which is equivalent to (21). □
In fact, (3) and (5) implies that the assumption of Lemma 3 is satisfied, hence (19) with in (5) satisfies (20).
2.4. Consistency Relations—Proof of Lemma 1
Lemma 1 confirms that the multi-species TASEP is integrable even when the rates are species-dependent.
2.4.1. Proof of Lemma 1 (a)
It suffices to show that
This equality clearly holds because both sides are equal to . □
2.4.2. Proof of Lemma 1 (b)—Yang-Baxter Equation
It suffices to show
If we re-arrange the columns and the rows of the matrices in (24) so that all their labels from the same multi-set are grouped together, then the matrices in (24) become block-diagonal (See Figure 1).
Figure 1.
Form of the matrices in (24) after re-ordering the rows and columns.
Let be the sub-matrix of whose rows and columns are labelled by the permutations of the multi-set , and similarly, we define . Then, in order to show (24), it suffices to show
for each multi-set whose elements are from because all matrices are block-diagonal matrices in the same form. If , (25) is equivalent to
which is trivially true. If , then (25) is equivalent to
which can be easily verified by direct computation. Similarly, the other two cases of (25) for and for the case that all are distinct can be verified by direct computation. □
2.4.3. Proof of Lemma 1 (c)
It suffices to show that . Let us re-arrange the rows and the columns in the same way as in the proof of Lemma 1 (b) to make and block-diagonal. Then, each block on the diagonal of is either a matrix or a matrix. The sub-matrix of consisting of the row and the column is . The sub-matrix of consisting of the rows and the columns with is
Similarly, the sub-matrix of consisting of the row and the column is , and the sub-matrix of consisting of the rows and the columns with is
It is trivial that , and this can be verified,
by the direct computation. □
2.5. Initial Condition
The contour integral of (19) multiplied by from the left and by from the right, that is, the right-hand side of (6) still satisfies (11) and (12). (The contour is the one introduced in Theorem 1). Hence, it remains to show that all transition probabilities satisfy the initial condition
where is the -element of . We will show that the integral with the identity permutation in the sum satisfies (26), and other integral terms with non-identity permutations are zero.
Proof.
If is the identity permutation, then is the identity matrix. Hence, if , then the integral is zero. It is easy to see that if and for all i, then the integral is 1. If and for some i (recall that our model is totally asymmetric), then the integral becomes zero when integrating with respect to . Now, suppose that is not the identity permutation. Note that the factors in are from (1), all poles arising from , if any, are outside the contours. There exists an i such that because each and is not the identity permutation. Hence, integrating with respect to i, the integral is 0. □
3. Conclusions
In this paper, we have shown that the Bethe ansatz method is still applicable to the multi-species TASEP with species-dependent rates. Theorem 1 provides the transition probabilities for all possible compositions of species, which is expected to be used to study further objects, such as the current distribution for certain special initial configurations. The methods used in this paper have limitations in extending to the ASEP () for now, but it would be interesting to see if the methods can be used to study the species-inhomogeneity of other multi-species models.
Funding
This research was funded by Nazarbayev University (Faculty Development Competitive Grant grant number 090118FD5341 and 021220FD4251.
Institutional Review Board Statement
Not applicable.
Informed Consent Statement
Not applicable.
Data Availability Statement
Not applicable.
Acknowledgments
The author is grateful to anonymous referees for providing valuable comments.
Conflicts of Interest
The author declares no conflict of interest.
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