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. 2017 Jul 1;168(4):794–825. doi: 10.1007/s10955-017-1827-6

Hydrodynamic Limit of Condensing Two-Species Zero Range Processes with Sub-critical Initial Profiles

Nicolas Dirr 1,, Marios G Stamatakis 2, Johannes Zimmer 2
PMCID: PMC6979527  PMID: 32025053

Abstract

Two-species condensing zero range processes (ZRPs) are interacting particle systems with two species of particles and zero range interaction exhibiting phase separation outside a domain of sub-critical densities. We prove the hydrodynamic limit of nearest neighbour mean zero two-species condensing ZRP with bounded local jump rate for sub-critical initial profiles, i.e., for initial profiles whose image is contained in the region of sub-critical densities. The proof is based on H.T. Yau’s relative entropy method, which relies on the existence of sufficiently regular solutions to the hydrodynamic equation. In the particular case of the species-blind ZRP, we prove that the solutions of the hydrodynamic equation exist globally in time and thus the hydrodynamic limit is valid for all times.

Keywords: Hydrodynamic limit, Zero range processes, Condensing zero range processes, Comparison principles for systems of PDEs

Introduction

In this article, we derive the hydrodynamic limit of a system of two interacting particle systems, specifically two-species zero range processes (ZRPs). The motivation for this study is that hydrodynamic limits provide effective descriptions of large scale interacting particle systems. There is a now good understanding of this limit passage for a range of particle processes leading to one hydrodynamic limit equation. In particular, Kipnis and Landim [19] establish the hydrodynamic behaviour for the one-species zero range process, using the entropy method of Guo, Papanicolaou and Varadhan [17]. For systems, however, this limit passage is less well studied, and several tools available for single equations are no longer available, as explained in more detail below. In particular, many systems where a hydrodynamic passage would be of interest both in its own right and as a tool to understand the limiting system of partial differential equations (PDEs) are currently inaccessible to the methods available; the full Patlak Keller-Segel system [18] modelling the evolution of cells or bacteria guided by the concentration of a chemical substance is an example. Yet, there are several recent studies focusing on different models of interacting particle systems. One avenue is to derive equations which incorporate aspects of underlying models, be it by considering the motion of cells only in a stationary, but random, environment mimicking the chemical [14], or by an equation with a singular potential related to a Green’s function describing the solution of a second equation [11]. The hydrodynamic limit system of an active exclusion process modelling active matter has been recently derived using a two-block estimate and non-gradient estimates [3].

Another approach is to study systems related to underlying zero-range processes (ZRPs) of several species to obtain a limiting system, and this is the approach we pursue here. The focus on ZRPs can be motivated by their nature as a toy model of an interacting particle system. We consider a system of two zero-range processes but the extension to n types is straightforward. Each ZRP is a process on a lattice where particles jump from one site to another according to a jump rate function depending on the number of the two species of particles on this site only (hence the name zero range).

The hydrodynamic limit in the Eulerian scaling ttN of asymmetric many-species ZRPs with product and translation invariant equilibrium states has been studied in [16]. The hydrodynamic limit in the parabolic scaling ttN2 for a class of processes not satisfying the assumptions of [16] has also recently been studied [26]; there one type of particles performs a random walk and influences the other type, which is a process of ZRP type. In general, establishing hydrodynamic limits for systems of equations rigorously is a hard problem, with few known results so far. To name a few, the hydrodynamic limit of a two-species simple-exclusion process was first studied in [21], the Leroux system has been derived as a hydrodynamic limit in [24], and hyperbolic systems have also been studied in [25].

Here we consider a system of two ZRPs. We show that the hydrodynamic equation is a quasilinear parabolic system of the form

tρ=ΔΦ(ρ),ρ=(ρ1,ρ2):[0,T)×TdAR+2, 1

where tρ:=(tρ1,tρ2), ΔΦ(ρ):=(ΔΦ1(ρ),ΔΦ2(ρ)) and Φ:AR+2 is the mean jump rate of the ZRP at a site xTNd under the product and translation invariant equilibrium state of background density ρAR+2. Two-species ZRPs, and the phase transition they exhibit, were first studied in [8]. In condensing ZRPs, the set A of admissible background densities ρ is a strict subset of R+2. We call such densities sub-critical.

One challenge of ZRPs is that they can exhibit condensation phenomena, where particles congregate at the same site [7, 9, 15]. Even for one-species systems, the hydrodynamic limit of ZRPs experiencing condensation is presently unknown. We consider parameter regimes of two-species systems where condensation can occur, but restrict to sub-critical initial profiles, i.e., initial data that take values in the set of sub-critical densities. For one-species ZRPs, the analogous result has been established recently [23] and we extend this argument to the two-species case. Specifically, we apply the relative entropy method of H. T. Yau [28], which requires only the one-block estimate proved in Theorem 3.1, not the full replacement lemma [19, Lemma 5.1.10]. Thus it does not require the equilibrium states of the ZRP to have full exponential moments, a property not satisfied by condensing ZRPs. This extension of [23] is non-trivial, for two reasons. The first difficulty is that the relative entropy method requires the existence of C2+θ solutions to (1) for some θ(0,1], and that the solution remains in the sub-critical region. By a result of Amann [1] it is know that, when starting from C2+θ initial data, C1,2+θ solutions of uniformly parabolic systems exist locally in time, i.e., for small time intervals, and are unique. Thus there exists a unique maximally defined classical solution of the parabolic system (1) taking values in the sub-critical region A. So our general result on the hydrodynamic limit is local in time, being valid for the largest time interval for which the unique maximal classical C1,2+θ solution with values in the sub-critical region exists. This result shows that at least for as long as the unique maximal classical solution to the parabolic system (1) is defined, condensation does not occur. The second difficulty to extend the results for one species [19, 23] is that the phase space R+2 is now more complicated, and the one-dimensional arguments used in [19, 23] do not extend directly. In particular, a novel argument is required to extend [19, Lemma 6.1.10]; see Lemma 4.5 and its proof. Specifically, we employ a characterisation of the domain of a convex function via the recession function of its Legendre transform. This characterisation of the domain of convex functions is of interest in its own right in the context of two-species ZRPs. For example, it immediately yields a parametrisation of the boundary of the domain of the partition function via the recession function of the thermodynamic entropy.

Intuitively, condensation means on the level of the governing hydrodynamic limit PDE the formation of singularities where the mass concentrates. For scalar equations, the formation of such singularities can be ruled out by a maximum principle. For systems, however, in general maximum principles do not hold. In this article, we mainly rely on an existence theory for local C1,2+θ classical solutions established by Amann and focus on proving the local in time hydrodynamic limit. However, for a particular example, the so-called species-blind process, we are able to establish a maximum principle and C1+θ,2+θ regularity for the hydrodynamic equation. This allows us to obtain that C1+θ,2+θ solutions exist and remain in the sub-critical region for all times. So in this particular case, the result on the hydrodynamic limit is global in time.

Maximum principles are more complicated for non-linear parabolic systems, since one has to determine the shape of the invariant region in which the solution will have to remain [6, 27], while in the scalar case the invariant region is just an interval. For the species-blind process we find that the invariant region of the hydrodynamic equation coincides with the sub-critical region of the ZRP. This is not surprising since the species-blind process is obtained from a one-species ZRP by colouring particles in two colours, say black and white. The dynamics is the usual ZRP dynamics but at each time of a jump from a site x, we choose the colour of particle to move with the probabilities given by the ratios of the number of black particles and white particles at x to the total number of particles at x, ignoring the colour. It would still be interesting to study the class of parabolic systems arising from two-species ZRPs in order to determine the largest class of ZRPs that their sub-critical region is an invariant region of the hydrodynamic limit. This would then provide a way to find the invariant region of the associated parabolic systems by calculating the phase diagram of the underlying ZRP. The study of the system of PDEs arising from the ZRP is a different topic and outside of the scope of this article, which mainly focuses on the passage from the microscopic to the macroscopic level by applying the relative entropy method.

Plan of the Paper

The paper is organised as follows. In Sect. 2 we collect some preliminary material on two-species ZRPs and describe the particular case of the species-blind ZRP. Section 3 contains the statements of the main results, and in Sect. 4 we give the proofs.

The Particle Model

We briefly give the definition of two-species ZRPs as Markov jump processes (Sect. A.1.2 in [19]) and their equilibrium states. Main references on this preliminary material are [12, 13]. We take the discrete d-dimensional N-torus TNd as underlying lattice. Each particle interacts only with particles in the same lattice site through a function g=(g1,g2):N02R+2. Here gi(k) is the jump rate of species of type i from any site that contains kN02 particles, i.e., ki particles of type i, for i=1,2. We impose the natural condition

gi(k)=0iffki=0,k=(k1,k2)N02 2

and require

igi:=supkN02|gi(k+ei)-gi(k)|<+, 3

where ei=(δij)j=1,2, i=1,2, are the unit vectors in R2. Note that setting g:=1g12g2<+, we have by (2) and (3) that

|g(k)|pg|k|p,for everykN02, 4

where |·|p denotes the p-norm in R2, p[1,+].

The state space of a two-species ZRP consists of all configurations η=(η1,η2):TNdN02, so that ηi(x) is the number of i-type particles at site x, for i=1,2. For any measurable space M we denote by P(M) the set of all probability measures on M. We write pP(Zd) for the nearest neighbour (n.n.) elementary step distribution given by

p(x):=12dj=1d1{-ej,ej}(x),xZd,

and by pNP(TNd) its projection on TNd given by pN(x):=p(x+NZd). Also, given a configuration ηMNd;2:=(N02)TNd, we will denote by ηi;x;y, i=1,2, the configuration resulting from η by moving a type-i particle from x to y. (If ηi(x)=0, then we set ηi;x;y=η.) The two-species n.n. symmetric ZRP with jump rate g on the discrete torus TNd:={0,1,,N-1}d is the unique Markov jump process on the Skorohod space D(R+;MNd;2) of càdlàg paths characterised by the formal generator

LNf(η)=i=1,2x,yTNd{f(ηi:x,y)-f(η)}gi(η(x))pN(y-x). 5

We will denote by (PtN)t0 the transition semigroup of the n.n. symmetric ZRP. The communication classes of the stochastic dynamics defined by the generator above are the hyperplanes

MN,Kd;2:={ηMNd;2|xTNdη(x)=K}

consisting of a fixed number of particles of each species. Since each set MN,Kd;2 is finite, for each (N,K)N×N02 there exists a unique equilibrium distribution νN,K supported on MN,Kd;2. The family {νN,K}(N,K)N×N02 is the so-called canonical ensemble. However, as proved in [12, Theorem 4.1], in order to have product and translation invariant equilibrium distributions, it is necessary and sufficient that the following compatibility relations for the component functions of two-species jump rates hold,

g1(k)g2(k-e1)=g1(k-e2)g2(k),for allkN02withk1,k21. 6

Note that due to the compatibility relations (6) any two-species local jump rate g is uniquely determined by g1 and the restriction of g2 to the set {0}×N0, since by induction for any kN02

g2(k)=g2(0,k2)i=0k1-1g1(k-ie1)g1(k-ie1-e2).

An increasing path γ (from 0) to kN02 is any path γ:{0,,k1+k2}N02 such that γ(0)=0, γ(k1+k2)=k and γ()=γ(-1)+ei for some i{1,2} for all =1,,k1+k2. For any increasing path γ to kN02, the factorial of g along γ is defined as

g!(k;γ)==1k1+k2gi(γ())

for k0; we set g!(·):=1 if k=0. A two-species local jump rate function g that satisfies (6) yields a well-defined function g!:N02(0,) by the formula

g!(k)=g!(k;γ)for some increasing pathγtok.

For instance

g!(k)=g1(1,0)··g1(k1,0)·g2(k1,1)··g2(k1,k2)=g2(0,1)··g2(0,k2)·g1(1,k2)··g1(k1,k2).

According to [12, Theorem 4.1], using the multi-index notation φk:=φ1k1φ2k2, with φ,kR+2, for two-species symmetric n.n. ZRP satisfying (6), the common one-site marginal ν¯φ1 of the product and translation invariant equilibrium states ν¯φN is given by the formula

ν¯φ1(k)=1Z(φ)φkg!(k),kN02,

for all φR+2 such that the series

Z(φ):=kN02φkg!(k) 7

converges. The function Z:R+2[1,+] defined in (7) is called the partition function. The main convexity property of Z is that the function Z:=Zexp:R2(1,+] is strictly logarithmically convex where exp(μ):=eμ:=(eμ1,eμ2). This can be seen by applying Hölder’s inequality to the functions keμ,k, keν,k with respect to the σ-finite measure λ on N02 given by λ(k):=1g!(k) and with the pair of conjugate exponents p=11-t, q=1t for t(0,1) and μ,νR2 such that μν, which yields

Z((1-t)μ+tν)=e(1-t)μ,ketν,kdλ(k)<Z(μ)(1-t)Z(ν)t.

Here and in what follows μ,k=μ1k1+μ2k2 denotes the Euclidean inner product of two vectors k,μR+2. We denote by DZ:={φR+2|Z(φ)<+} the proper domain of Z, which is a complete, i.e., [0,φ]:=[0,φ1]×[0,φ2]DZ for all φDZ, and logarithmically convex set, that, is the set DZ=log(DZ(0,)2):={logφ:=(logφ1,logφ2)|φDZ(0,)2} is convex. The partition function is C in DZo and continuous from below on DZ, i.e., for all φDZ, ε>0 there exists δ>0 such that |Z(φ)-Z(ψ)|<ε for all ψD(0,δ)[0,φ]. Here D(0,δ) denotes the Euclidean open ball of radius δ with centre 0 in R+2, i.e., D(0,δ)={φR+2||φ|2<δ}.

The family of the product and translation invariant equilibrium states is the family {ν¯φN}φDZ. This family is usually referred to as the grand canonical ensemble (GCE). In order to ensure that DZ is not trivial, i.e., that DZ contains a neighbourhood of zero in R+2, we must impose the following condition in the definition of two-species local jump rate functions:

φ;1:=lim inf|k|1+g!(k)1|k|1>0. 8

A two-species local jump rate g satisfies (8) iff DZ contains a neighbourhood of 0 in R+2. In what follows, we consider only two-species local jump rates that satisfy (6) and (8).

It is convenient to have a parametrisation of the GCE by the density. This is done via the density function R=(R1,R2):DZ[0,+]2 defined by

R(φ)=MNd;2η(0)dν¯φN=(k1dν¯φ1,k2dν¯φ1).

The proper domain of R is the set DR:=φDZ|R(φ)R+2 and by differentiation of bivariate power-series, we have that

R(φ)=φ·(logZ)(φ)on the setDRo=DZo, 9

where φ·ψ:=(φ1ψ1,φ2ψ2) denotes the pointwise product of two vectors φ,ψR+2. Furthermore, this formula extends to the set DZDZ if we interpret the directional derivatives i(logZ)[0,+] as derivatives from the left. With the conventions log0=- and e-=0 the densities ρR(DR) can also be parametrised via the chemical potential by the function R:=Rexp:DRR(DR), where DR=log(DR):={logφ[-,+)2|φDR}. For the parametrisation via the chemical potentials R(μ)=(logZ)(μ) for all μDRo(-,+)2, where Z=Zexp.

The density function R:R(DR)DR is invertible. Indeed, it is straightforward to check (e.g., see [13, (4.10)]) that for all φDRo(0,+)2,

DR(φ)=DR(logφ)1φ1001φ2=Cov(ν¯φ1)1φ1001φ2,

where Cov(ν¯φ1) denotes the covariance matrix

Cov(ν¯φ1)ij=kikjdν¯φ1-kiν¯φ1kjν¯φ1,i,j=1,2.

This implies that DR(φ) is diagonisable with strictly positive eigenvalues for all φDRo(0,+)2. Furthermore,

1R1(φ)2R2(φ)>0forallφDRo 10

and for φDRo such that φ1φ2=0, the matrix DR(φ) is triangular, and thus invertible. Therefore the density function R:DRoR(DRo) is invertible. The fact that R is invertible on all of its domain follows by [13, Proposition 2.3], according to which for every ρ(0,)2 there exists a unique maximiser Φ¯(ρ)DR(0,)2 for the thermodynamic entropy

S(ρ):=supφDZ(0,)2{ρ,logφ-logZ(φ)}=ρ,logΦ¯(ρ)-logZ(Φ¯(ρ)). 11

Obviously, for ρ=0 the supremum is attained at φ=0 (with the convention 0·(-)=0). Furthermore, since Z is non-decreasing with respect to each variable separately, for any ρR+2\{0} with ρ1ρ2=0, say ρ2=0, the maximisation problem (11) is reduced to the corresponding maximisation problem for one of the one-species jump rate g^1(k):=g1(k,0), kN0 and the supremum is attained at Φ¯(ρ1,0)=(Φ^1(ρ1ρ^c,1),0), where Φ^1, ρ^c,1 are the mean jump rate and critical density of the one-species jump rate g^1 (see [12, Sect. 5.2.1] for the one-species case). Thus for any ρR+2 there exists a unique maximiser Φ¯(ρ)DR for the thermodynamic entropy S(ρ). As in [13, Proposition 2.3] the function Φ:R+2DR is continuous, Φ:=Φ¯|R(DR)=R-1 is the inverse of R:DRR(DR) and

Φ¯(R+2\R(DR))=DRDR.

Furthermore R(DR) is closed in R+2 and R(DR)=R(DRDR). According to this result Φ¯:R+2DR is a left inverse for R, i.e., Φ¯R=ΦR=idDR and the function

Rc:=RΦ¯:R+2R(DR)

is a continuous projection on R(DR) with Rc|R(DR)=idR(DR), satisfying

Rc(R+2\R(DR))=R(DRDR)=R(DR).

In particular, R:DRR(DR) is a homeomorphism and R(DR)o=R(DRo).

Note that the thermodynamic entropy coincides with the Legendre transform of the convex thermodynamic pressure logZ:R2(0,+], that is,

S(ρ)=(logZ)(ρ)=supμR2{ρ,μ-logZ(μ)}. 12

Since (logZ)=R=Rexp, it follows by the formula for the derivative of the Legendre transforms that for all ρ(0,)2R(DRo) the supremum in (12) is attained at

S(ρ)=(logZ)-1(ρ)=R-1(ρ)=logΦ(ρ).

Since S is convex the matrix D2S(ρ)=D(logΦ)(ρ) is symmetric and strictly positive definite for all ρR(DRo)(0,+)2. The symmetry of D2S(ρ), ρR(DRo)(0,+)2, implies the relations

Φ2(ρ)2Φ1(ρ)=Φ1(ρ)1Φ2(ρ), 13

which extend to ρR(DRo) because Ri(φ)=0 if and only if φi=0, i=1,2 and DR(φ) is triangular for φDRo with φ1φ2=0. Equation (13) can be seen as the macroscopic analogue of the compatibility relations (6).

Using the inverse Φ of R on R(DR), we can parametrise the grand canonical measures ν¯φN, φDR, that have finite density via

νρN:=ν¯Φ(ρ)N,ρR(DR), 14

so that they are parametrised by their density. We will denote by νρ:=xZdνρ1, ρR(DR), the product measures on the configuration space Md;2:=(N02)Zd over the infinite lattice Zd. The logarithmic moment-generating function Λρ:=Λνρ1:R2(-,+] of the one-site marginal νρ1, ρDR, is defined by

Λρ1(λ):=logeλ,kdνρ1(k)=logZ(eλ·Φ(ρ))Z(Φ(ρ)). 15

Consequently, the product and translation invariant equilibrium states have some exponential moments for all ρR(DRo). They have full exponential moments iff DZ=R+2.

It is easy to verify that Φ(ρ) has a probabilistic interpretation as the one-site mean jump rate with respect to the product and translation invariant equilibrium state of density ρR(DR), that is

Φ(ρ)=g(η(0))dνρN,ρR(DR).

Since Φ¯=ΦRc, it follows by (4) that for all ρR+2

|Φ¯(ρ)|1|g(η(0))|1dνRc(ρ)Ng|η(0)|1dνRc(ρ)N=g|Rc(ρ)|1g|ρ|1. 16

One says that the 2-species ZRP is condensing when R(DR)R+2, in which case there exist densities ρR+2 for which there is no grand canonical equilibrium state of density ρ. Since R(DR) is non-empty and closed in R+2 it follows that R(DR)R+2 if and only if R(DR), and thus condensation occurs precisely when DRDR. By [13, Theorem 3.3] it follows that Rc(ρ)ρ, that is, Rc,i(ρ):=Ri(Φ¯(ρ))ρi, i=1,2, for all ρR2. One says that condensation of the i -th species, i=1,2, occurs at the density ρR+2 if Rc,i(ρ)<ρi. All cases are possible, that is, at a given density ρR+2 no condensation, condensation of exactly one species and condensation of both species simultaneously can occur. These cases induce an obvious partition of the phase space R+2.

As proved in [13], the extension Φ¯ is the correct one for the equivalence of ensembles in the sense that Rc gives the correct limiting background density in the thermodynamic limit. In the case of condensation, i.e., when R(DR)R+2, some additional assumption must be imposed on the jump rate g to ensure that for each φDRDR, the one-site marginal ν¯φ1 has heavy tails in the direction normal to the set log(DRDR):={logφ|φDRDR} at μ:=logφ. Denoting by nφ the normal to log(DRDR) at logφ (where n(φ1,0)=e1, n(0,φ2)=e2), this means that

lim|kn|2+kn/|kn|2nφ1|kn|2logν¯φ1(kn)=0. 17

In case DR is not differentiable at φ, (17) is required to hold for the two limiting normal vectors nφ+, nφ- at logφ. As has been proven in [13, Lemma 3.5], a condition on the jump rate g that guarantees the critical equilibrium states have heavy tails in the direction normal to the logarithm of the boundary is the regularity of its tails, in the sense that for any direction υS+1:=S1R+2,

φc;2(υ):=lim inf|k|2+k/|k|2υg!(k)1|k|2(0,) 18

exists as limit and φc;2:S+1(0,) is a continuous function of the direction υS+1. Note that instead of the exponent p=2, we could have used any p[1,+], replacing the Euclidean sphere S+1 with the sphere Sp,+1:={xR+2||x|p=1} with respect to the p-norm on R+2. According to the equivalence of ensembles [13, Theorem 3.1], if the jump rate has regular tails when R(DR)R+2, then for all ρR+2

limN,|K|+K/Ndρ1NdHνN,K|νRc(ρ)N=0. 19

Here H(μ|ν) denotes the relative entropy between two probability measures μ,ν,

H(μ|ν):=dμdνlogdμdνdνifμν+otherwise.

The translation invariance of canonical and grand canonical ensembles and the super-additivity of the relative entropy imply convergence for any finite set FZd, i.e.,

limN,|K|+K/NdρHνN,KF|νRc(ρ)N,F=0

where νN,KF:=pFνN,K, νRc(ρ)N,F:=pFνRc(ρ)N are the push-forwards via the natural projection pF:MNd;2(N02)F and TNd is considered embedded in Zd. In turn this implies that νN,K (considered embedded in the larger space Md;2) converges as K/Ndρ to νRc(ρ) weakly with respect to bounded cylinder functions f:Md;2R, that is, such that they depend on a finite number of coordinates.

Finally, we briefly recall the notions of local equilibrium and hydrodynamic limits and refer to [19] for more details. We say that a sequence of probability measures {μNP(MNd;2)} is an entropy-local equilibrium of profile ρC(Td;R(DR)) if

lim supN+1NdHμN|νρ(·)N=0. 20

Here νρ(·)N:=xTNdνρ(x/N)1 is the product measure with slowly varying parameter associated to the profile ρC(Td;R(DR)). Given any cylinder function f:MNd;2R, we set f~(ρ):=fdνRc(ρ)N, ρR+2. By a simple adaptation of [19, Corollary 6.1.3], if {μN} is an entropy-local equilibrium of profile ρC(Td;R(DR)), then

limN+EμN|1NdxTNdH(xN)τxf(η)-TdH(u)f~(ρ(u))du|=0 21

for all HC(Td) and all bounded cylinder functions f:MNd;2R, that is, μN is a weak local equilibrium of profile ρC(Td;R(DR)).

The hydrodynamic limit (in the diffusive timescale ttN2) of the n.n. two-species ZRP is an evolutionary PDE, such that entropy-local equilibria are conserved along its solutions (in the diffusive time-scale) in the following sense: If we start the process from an entropy local equilibrium μ0NP(MNd;2), NN, of some sufficiently regular initial profile ρ0:TdR+2 at time t=0 and if there exists a sufficiently regular solution ρ of the hydrodynamic equation on [0,T)×Td starting from ρ0, then μtN:=μ0NPtN2N is an entropy-local equilibrium of profile ρ(t,·) for each t[0,T).

The main goal of this article is to apply the relative entropy method of H.T. Yau in order to prove the hydrodynamic limit of condensing two-species ZRPs that start from an initial entropy-local equilibrium {μ0N} of sub-critical and strictly positive profile ρ0C(Td;R(DRo)(0,)2), which is stated as Theorem 3.2 below. A main ingredient in the proof of the hydrodynamic limit is the one-block estimate which is stated as Theorem 3.1. The relative entropy method also requires the existence of a Cloc1,2+θ classical solution ρ:[0,T)×TdR(DRo)(0,+)2 for the hydrodynamic limit and applies the Taylor expansion for C2+θ functions to the function Φ(ρt) of the solution ρt at each time t>0 (see (45)) in order to estimate the entropy production tH(μtN|νρt(·)N). The sub-criticality of the solution ρ, i.e., that ρ([0,T)×Td)R(DRo), is used in Lemma 4.2 and to obtain the bound (52), which is essential in the application of Lemma 4.5. The sub-criticality of the solution ρ is also required for the application of the large deviations Lemma 4.4. Together with the C2+θ regularity of ρt for each t0 it is the main assumption on the solution ρ. Furthermore, in the Taylor expansion the quantities Φi(ρt), i=1,2, appear in the denominator, so we have to assume that the solution ρ is coordinate-wise strictly positive.

As already mentioned in the introduction the expected hydrodynamic limit of the two-species ZRP with product measures is a quasilinear parabolic system of the form (1), which in divergence form is given by

tρ=divAΦ(ρ,ρ). 22

Here the divergence with respect to the spatial parameter is applied coordinate-wise, and ρ(t,u):=(ρ1(t,u),ρ2(t,u))R2×d is the gradient of ρ with respect to the spatial variable uTd. Furthermore, AΦ=(AΦ1,AΦ2):R(DRo)×R2×dR2×d is the function given by

AΦ(ρ,V)=DΦ(ρ)V,

that is,

tρi=divAΦi(ρ,ρ)=div(Φi(ρ)ρ)=ΔΦi(ρ),i=1,2.

Structural properties of the mobility matrix DΦ:R(DRo)R2×2 can be inferred by the properties of DR. For example, for all ρR(DRo)(0,+)2,

DΦ(ρ)=Φ1(ρ)00Φ2(ρ)D2S(ρ),

where D2S(ρ)=D(logΦ)(ρ) is a strictly positive definite matrix, the second derivative of the thermodynamic entropy, and for all ρR(DRo), the relations (13) hold and

1Φ1(ρ)2Φ2(ρ)>0.

In particular, DΦ(ρ) has positive eigenvalues for all ρR(DRo) and is diagonisable for all ρR(DRo)(0,+)2. For ρR(DRo) with ρ1ρ2=0, the matrix DΦ(ρ) is triangular. It follows that although DΦ(ρ) is not necessarily symmetric, it is uniformly parabolic away from the critical densities, that is, for any compact KR(DRo) the exists λK>0 such that

ξ,DΦ(ρ)ξλK|ξ|2,ρK,ξR2.

By the work [1] of Amann, it is known that for C2+θ initial data, uniformly parabolic systems in general form have unique maximal C1,2+θ solutions. Thus, since DΦ is uniformly parabolic in any compact subset of R(DRo), it follows that for initial data ρ0C2+θ(Td;R(DRo)(0,+)2) there exists a unique maximal classical Cloc1,2+θ solution ρ:[0,Tmax)×TdR(DRo) of the parabolic system (1) taking values in the sub-critical region R(DRo). Of course, since we also assume ρ0(Td)(0,+)2, by taking if necessary Tmax to be smaller we can assume that ρ takes values in R(DRo)(0,+)2. This establishes the local in time existence of C1,2+θ sub-critical solutions ρ. On the other hand, by the regularity theory of quasilinear uniformly parabolic systems of the form (22), see [5, Theorem 1.2] and the references therein, it is known that weak solutions to such systems exhibit singularities on a closed subset Q[0,T]×Td of zero measure. So we can not simply apply the C2+θ Taylor expansion on the function Φ(ρt) for all times t0. Furthermore we do not know whether the sub-critical region R(DR) is an invariant region for the zero range parabolic system (22). These are the two main reasons that force us to rely on Amann’s local in time existence of regular solutions, and prove a local in time version of the hydrodynamic limit. A further study of the PDE system arising as the hydrodynamic limit of a two-species ZRP, although interesting, is outside of the scope of this article, which is the passage from the microscopic to the macroscopic description.

However, in the example of the species-blind ZRP one can take into advantage its relation with a particular one-species ZRP to obtain the global in time existence of Cloc1+θ,2+θ solutions and a type of maximum principle, in which the sub-critical region plays the role of the invariant domain. We prove this in Theorem 3.3.

The Species-Blind ZRP

We now consider two-species local jump rate functions of the form

g1(k)=k1h(k1+k2),g2(k)=k2h(k1+k2) 23

for some function h:N0R+ satisfying the non-degeneracy condition h(k)>0 for all kN. Any jump rate g of this form satisfies (6) since

g1(k)g2(k-e1)=k1h(k1+k2)k2h(k1+k2-1)=g1(k-e2)g2(k)

for all kN2 and the factorial of such a jump rate is given by

g!(k)=1·h(1)··k1·h(k1)·1·h(k1+1)··k2·h(k1+k2)=k1!k2!h!(k1+k2).

The partition function associated to g is given for φN02 with φ2>0 by

Z(φ)=m=0φ2mh!(m)k1=0mφ1φ2k1k1!(m-k1)!=m=0φ2mm!h!(m)(1+φ1φ2)m=Z^(φ1+φ2),

where Z^ is the partition function associated to the one-species rate function g^(k):=kh(k). So, in what follows, we assume that h is of the form h(k)=g^(k)k, k1, for some one-species local jump rate function g^ with regular tails, i.e., such that the limit inferior φ^c:=lim infk+g^!(k)1k>0 exists as a limit. In this case the function g defined in (23) is a two-species local jump rate. Indeed, the non-degeneracy condition (2) and the Lipschitz condition (3) are easy to verify, as we have seen g satisfies the compatibility condition (6) and obviously DZ={φR+2|φ1+φ2DZ^} and DR={φR+2|φ1+φ2DR^}, where R^(φ)=φ(logZ^)(φ) is the density function associated to the one-species jump rate g^. In particular DZ and thus also (8) holds. We will refer to this nearest neighbour two-species ZRP as the species-blind ZRP corresponding to the 1-species jump rate g^. The density function corresponding to g is given by the formula

R(φ)=(φ1Z^(φ1+φ2)Z^(φ1+φ2),φ2Z^(φ1+φ2)Z^(φ1+φ2))=R^(|φ|1)|φ|1φ.

We set Φ^:=R^-1 and we will compute the inverse Φ of R:DRR+2 in its image R(DR). Let ρ=R(φ). We have to solve the system

ρ1=φ1Z^(φ1+φ2)Z^(φ1+φ2),ρ2=φ2Z^(φ1+φ2)Z^(φ1+φ2) 24

for (φ1,φ2). By adding the two equations we obtain that ρ1+ρ2=R^(φ1+φ2). In particular ρ1+ρ2R^(DR^) for all ρR(DR) and φ1+φ2=Φ^(ρ1+ρ2). Substituting φ1+φ2 with Φ^(ρ1+ρ2) in both equations in (24), we can solve for (φ1,φ2) to obtain

φi=ρiZ^(Φ^(ρ1+ρ2))Z^(Φ^(ρ1+ρ2))=ρi1(logZ^(Φ^(ρ1+ρ2))=ρiΦ^(ρ1+ρ2)ρ1+ρ2,

where the last equality above follows from the identity R^(φ)=φ(logZ)(φ) for the one-species density and partition functions, since by this identity we have for all ρ(0,ρ^c) that

1(logZ^)(Φ^(ρ))=Φ^(ρ)R^(Φ^(ρ))=Φ^(ρ)ρ,

where ρ^c is the corresponding critical density of the one-species jump rate g^. Consequently, the inverse Φ:=R-1:R(DR)DR is given by the formula

Φ(ρ)=(ρ1Φ^(ρ1+ρ2)ρ1+ρ2,ρ2Φ^(ρ1+ρ2)ρ1+ρ2)=Φ^(|ρ|1)|ρ|1ρ. 25

Thus the expected hydrodynamic equation of the species-blind ZRP is

tρi=Δ(ρiΦ^(ρ1+ρ2)ρ1+ρ2),i=1,2. 26

Since (26) is the expected hydrodynamic equation of the species-blind ZRP we will refer to it as the species-blind parabolic system. A classical solution to the species-blind parabolic system is a C1,2 function ρ=(ρ1,ρ2):[0,T)×TdR2 satisfying (26) with 0ρ1(t,u)+ρ2(t,u)<ρ^c for all (t,u)[0,T)×Td. Note that for any classical solution ρ=(ρ1,ρ2) of the species-blind parabolic system (26) the sum ρ1+ρ2 satisfies the parabolic equation tρ=Φ^(ρ) corresponding to the 1-species ZRP of jump rate g^(k)=kh(k). This remark will allows us to prove the global in time existence of solutions to the species-blind parabolic system. A similar argument was used for two-species simple exclusion processes in [21].

As an example of the nice properties of the species-blind process, we note that the extended mean jump rate Φ¯:R+2DR of the species-blind process can be computed explicitly and is given by

Φ¯(ρ)=Φ^¯(|ρ|1)|ρ|1ρ,

where Φ^¯(ρ)=Φ^(ρρ^c), ρ0, is the extended mean jump rate of the one-species ZRP with jump rate g^.

Main Results

A main probabilistic ingredient in the proof of the hydrodynamic limit of ZRPs is the so-called one-block estimate, which is well known under assumptions that exclude condensing ZRPs (e.g., [19, Sect. 5.4]). Our first result is a version of the one-block estimate for condensing ZRPs, i.e., R(DR)R+2, under the additional assumptions that the local jump rate g is bounded, has a continuous partition function Z, and has regular tails in the sense of (18). We note that these extra assumptions in the one-block estimate and the hydrodynamic limit below are not required in the non-condensing case, i.e., when R(DR)=R+2. In the case that R(DR)=R+2, but DZR+2, Theorems 3.1 and 3.2 still hold under the (weaker than boundedness) assumption that g has sub-linear growth at infinity in the sense that

lim sup|k|1+|g(k)|1|k|1=0. 27

In the case that R(DR)=DZ=R+2, no extra assumption is required on g. Given any (cylinder) function f:MNd;2R2 we set

f:=1(2+1)d|x|τxf,

where τxf(η):=f(τxη) and τxη(y):=η(x+y) for x,yTNd.

Theorem 3.1

(One-block estimate) Suppose that the ZRP is condensing and that the local jump rate g of the ZRP is bounded, has regular tails in the sense of (18) and its partition function Z is continuous on DZDZ. Then for any sequence of initial distributions μ0NP(MNd;2) satisfying the O(Nd)-entropy assumption, i.e.,

C(a):=lim supNN1NdHμ0N|νaN<+, 28

for some (and thus for any) aR(DRo)(0,)2, it holds that

limlim supNEN|0T1NdxTNdF(t,xN),g(ηt(x))-Φ¯(ηt(x))dt|=0 29

for all functions FC([0,T]×Td;R2), T>0; EN denotes the expectation with respect to the diffusively accelerated law of the ZRP starting from μ0NP(MNd;2) and Φ¯ is the extension of Φ given by (11).

We note that the extension Φ¯ of the mean jump rate is required in the statement of the one-block estimate, because ηt can be outside the domain of sub-critical densities. This is the correct extension due to the equivalence of ensembles. The proof of this result is given in Sect. 4.1 below.

Next is the general result regarding the hydrodynamic limit of two-species ZRPs. As noted in the introduction, in order to take into account condensing ZRPs, we apply the relative entropy method of H.T. Yau which requires only the one-block estimate and not the full replacement lemma. But this method relies on the existence of sufficiently regular classical solutions of parabolic systems which are known to exist only locally in time, and thus the result is local in time, valid for the time interval that the unique maximal classical solution of (1) established in [1] exists. We denote by C1+a,2+b([0,T]×Td), a,b[0,1), the space of all C1,2-functions f:[0,T]×TdR such that tfCa([0,T]×Td) is a-Hölder continuous and ij2fCb([0,T]×Td) is b-Hölder continuous, where [0,T]×Td is equipped with the parabolic metric d given by

d((t,x),(s,y))=(dTd(x,y)2+|t-s|)12.

As usual, if IR is an interval, then we write Cloc1+a,2+b(I×Td) for the space of all functions f such that fC1+a,2+b(J×Td) for any compact sub-interval JI. This is extended coordinate-wise to vector-valued functions; given a subset AR2, we denote by Cloc1+a,2+b(I×Td;A) the subset of Cloc1+a,2+b(I×Td;R2) consisting of functions taking values in A.

Theorem 3.2

(Hydrodynamic limit) Let (StN)t0 be the transition semigroup of the two-species symmetric n.n. ZRP on the torus TNd, NN, with condensing jump rate g satisfying the assumptions of the one-block estimate above, and let Φ be the mean jump rate associated to g. Let

ρCloc1,2+θ([0,Tmax)×Td;R(DRo)(0,)2)

be the unique maximal solution of the parabolic system (1) with values in the sub-critical region R(DRo)(0,+)2 of strictly positive densities. Then any initial entropy local equilibrium μ0NP(MNd;2) is conserved along the solution ρ. In other words, if {μ0N} is an entropy-local equilibrium of profile ρ0:=ρ(0,·)C2+θ(Td) then μtN:=StN2Nμ0N, with NN, is an entropy local equilibrium for all t[0,Tmax). In particular, {μtN} satisfies (21) for all t[0,Tmax).

This theorem is proved in Sect. 4.2. We should note that, although the proof of the hydrodynamic limit relies strongly on the assumption that the classical solution ρ takes values in the set R(DRo)(0,)2 for all times t0, and so in particular requires the sequence of initial distributions {μ0N} to be an entropy local equilibrium of some sub-critical and strictly positive profile ρ0ρ(0,·), the one-block estimate does not require this assumption. It only requires that {μ0N} satisfies the O(Nd)-entropy assumption, which can hold even for super-critical profiles, having a Dirac mass of order O(Nd) at some site xTd, e.g., μ0N(dη)=δ[aNd](dη[Nx])y[Nx]νρ(y/N)1(dηy) with a(0,)2, when R(DR)R+2.

We note also that the assumption that ρ([0,Tmax)×Td)(0,+)2 is a technical one, arising from the fact the Φ(ρt) appears in the denominator. If one knew that the region R+2 is strongly invariant for the parabolic system (1) in the sense that ρ1ρ2 becomes strictly positive (and sufficiently fast) for the solution ρ, then one can replace the assumption ρ([0,Tmax)×Td)(0,+)2 with the assumption ρ00 as in [23, Remark 3.3] for the one-species case. Secondly, if one knew that the region (0,+)2 is invariant for the parabolic system (1), then starting from C2+θ non-negative initial data ρ0:TdR(DRo) one could could choose small enough ε>0 such that ρ0ε(Td)R(DRo)(0,+)2 where ρ0,iε=ρ0,i+ε, i=1,2, use the result for strictly positive data and try to pass to the limit as ε0. Since we do not pursue the study of the quasilinear parabolic system (1) and its invariant regions at the macroscopic level in this article, we consider only local solutions which are strictly positive and sub-critical and whose existence is established by Amann [1].

The next result states that, when starting from sufficiently regular subcritical initial profiles, the species-blind system (26) has solutions defined globally in time.

Theorem 3.3

(Global existence for the species-blind parabolic system) Let ρ0C2+θ(Td;R(DRo)(0,)2), θ[0,1), be an initial profile. Then the species-blind parabolic system (26) has a unique classical solution ρ:R+×TdR2 starting from ρ0 and

ρCloc1+θ,2+θ([0,+)×Td;R(DRo)(0,)2).

The proof of this Theorem can be found in Subsect. 4.3 and it is obtained by taking into account the fact that the sum ρ1+ρ2 of the two variables of a solution ρ=(ρ1,ρ2) of the species-blind parabolic system is a solution of the scalar parabolic equation t(ρ)=ΔΦ^(ρ). Here, by using the strong maximum principle for scalar quasilinear parabolic equations and by proving that classical solutions ρ of the species-blind parabolic system do not become negative, we obtain that the the sub-critical region is an invariant region. We believe that R+2 will be an invariant region of the species-blind parabolic system in general. Yet, since we do not study this question in this article, in order to be rigorous we prove it in this particular case. We should add that the arguments used strongly rely on the relation to the PDE of the single species ZRP associated to the species-blind ZRP by “ignoring” the species, and thus do not easily extend to the general case.

As a corollary, we find that the hydrodynamic limit for the species-blind process holds globally in time; Subsect. 4.4 gives the proof.

Corollary 3.1

Let (StN)t0 be the transition semigroup of the diffusively rescaled species-blind symmetric n.n. ZRP on the torus TNd corresponding to a one-species jump rate g^ such that φ^c:=lim infk+g^!(k)1k(0,+] exists as a limit. Assume further that g^ is bounded if the critical density ρ^c of the one-species ZRP is finite. If μ0NP(MNd;2) is an entropy local equilibrium of profile ρ0C2+θ(Td;R(DRo)(0,)2), then μtN:=μ0NStN is an entropy local equilibrium of profile ρ(t,·) for all t0, where ρCloc1+θ,2+θ(R+×Td;R(DRo)(0,)2) is the unique solution to the species-blind parabolic system (26) starting from ρ0.

Proofs

Proof of Theorem 3.1

The proof of the one-block estimate follows closely the proof for the one-species case found in [19, Sect. 5.4]. The differences are twofold. In [19, Sect. 5.4], the one-species case is treated, and we extend this result to two species. However, the main difference is that in [19] the non-condensing case is treated, while we cover the condensing case as well. This is shown by applying the equivalence of ensembles (19) as in [23].

The first step in the proof of the one-block estimate is to replace the jump rate g(η(x)) at the site x with the spatial average g(η(x)) over a box of size N0. This is based on the following lemma which is also useful in the proof of Theorem 3.2. The proof is omitted as it is a simple adaptation of the proof for the one-species case [19, Lemma 6.4.1].

Lemma 4.1

If the sequence {μ0N} of initial distributions satisfies the O(Nd)-entropy assumption (28), then

|η|1dμ0NO(Nd),

where |η|1:=|η|N,1:=xTNd|η(x)|1.

This lemma, a change of variables and the conservation of the number of particles allow us to replace g(η(x)) with the spatial average g(η(x)) in the statement of the one-block estimate, and thus the one-block estimate is reduced to proving that

limlim supN1NdxTdτxVdμ¯TN=0, 30

where μ¯TN:=1T0TμtNdt and V is the cylinder function V:=|g(η(0))-Φ¯(η(0))|1.

We establish this identity in a sequence of steps. We first estimate the entropy and the Dirichlet form of the density f¯TN:=dμ¯TN/dνρN of μ¯TN with respect to an equilibrium state of density ρA. Note that f¯TN=1TftNdt, where ftN:=dμtN/dνρN is the density of the law μtN of the ZRP at time t with respect to the product equilibrium state of density ρA. By [19, Proposition A.9.1], for any initial probability measure μ the entropy H(μt|ν) of the law μt:=μPt of a Markov semigroup (Pt)t0 at time t with respect to an equilibrium state π of (Pt) is a non-increasing function of time. Here the equilibrium π need not be unique or approached by μt as t+. Therefore, since μ0N satisfies the O(Nd)-entropy assumption, we have for fixed ρA that H(μtN|νρN)C(ρ)Nd, which, by convexity of the entropy, implies that H(μ¯TN|νρN)C(ρ)Nd. Furthermore, if DN:L+1(νρN)[0,+] denotes the functional defined by DN(f)=DN(f) where DN:L2(νρ)[0,+] is the Dirichlet form associated to the generator LN,

DN(f):=-f,LNfνρ=-fLNfdνρ,

then by [19, Proposition A.9.2] and the convexity of the functional DN, it follows that DN(f¯TN)1T0TDN(ftN)dtC(ρ)2TNd-2. Therefore, if we set HN(f):=H(fdνρN|νρN), in order to prove the one-block estimate, it suffices to prove that for some ρA

lim suplim supNsupHN(f)C0NdDN(f)C0Nd-21NdxTNdτxVfdνρN0,C0>0, 31

where the supremum is taken among all densities fL+1(νρN).

In a second step, following the proof of the one-species case [19, Sect. 5.4] we cut off large densities. Since Lemma 4.1 requires only the O(Nd)-entropy assumption, it follows that

lim supN+supHN(f)CNd1Nd|η|1fdνρN<+,for everyC>0. 32

Similarly to the one-species case, under the assumption that g has sublinear growth at infinity in the sense of (27) (which always holds when g is bounded), inequality (32) allows us to cut off large densities, by restricting V to the set of configurations η which satisfy |η(0)|1C1 for some constant C1>0. This way the one-block estimate is reduced to proving that for all constants C0,C1>0

lim+lim supN+supDN(f)C0Nd-21NdxTNdτxV1{|η(x)|1C1}fdνρN0. 33

In a third step, by adapting the steps 2 to 4 of [19, Sect. 5.4.1] to the two-species case, the one-block-estimate is further reduced to showing that for all constants C1>0,

lim sup+maxK||K|1(2+1)dC1Vdν2+1,K=0, 34

where the canonical measure ν2+1,K is considered as a measure on Md by identifying the cube Λd:={xZd||x|}Zd with T2+1d.

The final step in the proof of the one-block estimate consists in applying the equivalence of ensembles to prove (34). Since the measure ν2+1,K is concentrated on configurations with K particles, the integral appearing in (34) is equal to

Vdν2+1,K=|1(2+1)d|x|g(ξ(x))-Φ¯(K(2+1)d)|1dν2+1,K.

As in the one-species case, by fixing a positive integer k which will tend to infinity after taking the limit as +, and decomposing the cube Λd in smaller cubes of side-length 2k+1, the one-block estimate is reduced to showing that

limklimmS(m,k)=0, 35

where S(mk) denotes the supremum

S(m,k):=supm|K|1(2+1)dC1|1(2k+1)d|x|kg(ξ(x))-Φ¯(K(2+1)d)|1dν2+1,K.

This is the part of the proof where we need the boundedness and the regularity of the tails (18) of the jump rate g as well as the continuity of the partition function Z on DZDZ. For each fixed (m,k)N×N, we pick a sequence {(nm,k,Knm,k)}nN such that nm,km and |Knm,k|1(2nm,k+1)dC1 for all nN that achieves the supremum, i.e., such that

S(m,k)=limn|1(2k+1)d|x|kg(ξ(x))-Φ¯(Knm,k(2nm,k+1)d)|1dν2nm,k+1,Knm,k.

Since the sequence {rnm,k}nN defined by

rnm,k:=Knm,k(2nm,k+1)d,nN,

is contained in the compact triangular region B|·|1(0,C1):={rR+2||r|1C1}, for each fixed (m,k)N×N, we can pick a sequence {nj}jN:={njm,k} such that rnjm,k converges to some rm,kB|·|1(0,C1) as j. Since we assume that g is bounded, it follows by the equivalence of ensembles that

S(m,k)=|1(2k+1)d|x|kg(ξ(x))-Φ¯(rm,k)|1dνRc(rm,k).

Furthermore, since |Rc(ρ)|1|ρ|1, for each fixed kN the sequence {ρm,k:=Rc(rm,k)}mN, is also contained in B|·|1(0,C1) and thus we can choose a sequence {mj}jN={mj(k)} such that {ρmj,k}mN converges to some ρkB|·|1(0,C1)R(DR). By the continuity assumption on Z, the grand canonical ensemble is weakly continuous. By this fact, the continuity of Rc and the identity Φ¯=ΦRc,

limmS(m,k)=|1(2k+1)d|x|kg(ξ(x))-Φ(ρk)|1dνρk.

Therefore

lim supk+limm+S(m,k)lim supksupρR(DR)|1(2k+1)d|x|kg(η(x))-Φ(ρ)|1dνρ.

The random variables g(η(x)), xZd, are uniformly bounded by g and i.i.d. with respect to νρ for all ρR(DR) and thus they satisfy the L2-weak law of large numbers uniformly over all parameters ρR(DR), which shows that the term in the right hand side above is equal to zero. This completes the proof of the one-block estimate and hence the proof of Theorem 3.1.

Proof of Theorem 3.2

Let A be the interior of the set of all strictly positive sub-critical densities, i.e.,

A:=R(DRo)(0,)2,

and let ρ:[0,Tmax)×TdA be the maximal classical solution established in [1] of the initial value problem (1) with ρ(0,·):=ρ0C2+θ(Td;A). We fix aA and denote by ψtN the Radon-Nikodym derivative of νρt(·)N with respect to νaN,

ψtN:=dνρt(·)NdνaN.

Let HN(t):=H(μtN|νρt(·)N) be the relative entropy of μtN with respect to νρt(·)N. We have the following upper bound on the entropy production, proved in [19, Lemma 6.1.4],

tHN(t)1ψtN{N2LNψtN-tψtN}dμtN 36

for every t[0,Tmax), where LN is the adjoint of LN in L2(νaN). Denoting by

H(t):=lim supN1NdHN(t),t[0,Tmax), 37

the limiting entropy density, the main step in the application of the relative entropy method is to use this upper bound on tHN(t) to get an inequality of the form

H(t)H(0)+1γ0tH(s)ds 38

for some constant γ>0. Since H(0)=0 by assumption, this implies by Gronwall’s inequality that H(t)=0 for all t[0,Tmax) as required. Of course, in order for Gronwall’s inequality to be applicable, H must belong at least in Lloc1([0,Tmax)]. This is the context of the next two lemmas. The first is Remark 6.1.2 in [19] for single-species ZRPs.

Lemma 4.2

If {μ0N} is an entropy local equilibrium of profile ρC(Td;R(DRo)), then {μ0N} satisfies the O(Nd)-entropy assumption (28).

Proof

Indeed, for fixed aA:=R(DRo)(0,)2, by the relative entropy inequality [19, Sect. A.1.8]

H(μ0N|νaN)(1+1γ)H(μ0N|νρ(·)N)+1γlogeγlogdνρ(·)NdνaNdνρ(·)N. 39

Since νρ(·)N, νaN are product measures, the Radon-Nikodym derivative dνρ(·)NdνaN can be computed explicitly. With the notation Φa:=(Φ1Φ1(a),Φ2Φ2(a)), Za:=ZΦZ(Φ(a))

(dνρ(·)NdνaN)γdνρ(·)N=xTNd1Za(ρ(x/N))γek,γlogΦa(ρ(x/N))dνρ(x/N)1(k).

Since Z1, we have that 1Za(ρ)=Z(Φ(a))Z(Φ(ρ))Z(Φ(a)) and therefore

1γNdlog(dνρ(·)NdνaN)γdνρ(·)NZ(Φ(a))+1γNdxTNdΛρ(x/N)(γlogΦa(ρ(x/N)))Z(Φ(a))+1γNdxTNdlogZ(Fa(x/N,γ)), 40

where here Fa:Td×[0,1](0,)2 is the function given by Fa(u,γ)=Φ(ρ(u))1+γΦ(a)γ and for aR+2, b(0,)2, γ>0, we have set aγ:=(a1γ,a2γ) and ab:=(a1b1,a2b2). Since ρ(Td)R(DRo) by assumption, it follows that Φ(ρ(Td))DZo. Since Fa is uniformly continuous on Td×[0,1] and satisfies limγ0Fa(u,γ)=Φ(ρ(u)) for all uTd, it follows that its image is contained in DZo, i.e., {Fa(u,γ)|uTd}DZo for sufficiently small γ>0. Then the function uZ(Fa(u,γ)) is well defined and continuous on the torus Td, so that its Riemannian sums converge. By (39), (40) and the fact that μ0N is an entropy local equilibrium, this yields that

C(a)Z(Φ(a))+1γTdlogZ(Fa(u,γ))du<+

for small γ>0, and the proof of Lemma 4.2 is complete.

Lemma 4.3

Let ρ:[0,T]×TdR(DRo)(0,)2 be a continuous function and let {μ0N} be an entropy local equilibrium with respect to ρ0:=ρ(0,·). Then the upper entropy H¯:[0,T][0,+] defined by

H¯(t):=supNN1NdHμtN|νρt(·)N

belongs to L([0,T]).

Proof

By the relative entropy inequality and [19, Proposition A.1.9.1], according to which the function tH(μtN|νaN) is non-increasing,

HN(t)(1+1γ)H(μ0N|νaN)+1γlog(dνaNdνρt(·)N)γdνaN 41

for all t0 and all γ>0. Since the proper domain of Za has interior DZao=R(DRo) and since ρ([0,T]×Td)R(DRo)(0,)2, the function Zaρ is a bounded continuous function on the torus, and therefore, by a computation similar to the one in the proof of Lemma 4.2, we obtain

1γNdlog(dνaNdνρt(·)N)γdνaN=ZaρL([0,T]×Td)+1γNdxTNdΛa(γlog1Φa(ρt(x/N))),

where ZaρL([0,T]×Td)<+. For the second term, we have for every uTd that

Λa(γlog1Φa(ρt(u)))=log{1Z(Φ(a))Z(Φ(a)1+γΦ(ρt(u))γ)}. 42

Since Φ(ρ)(Td)(0,)2 and Φ(ρ) is continuous, there exists φ0DZ such that φ0<Φ(ρ(t,u)) for all (t,u)[0,T]×Td. Then since Z is increasing,

Z(Φ(a)1+γΦ(ρt(u))γ)Z(Φ(a)1+γφ0γ),

and since Φ(a)DZo and Φ(a)1+γ/φ0γΦ(a) as γ0, we can choose γ0>0 sufficiently small so that Φ(a)1+γ/φ0γDZo and Z(Φ(a)1+γ/φ0γ)Z(Φ(a))+1 for all γ<γ0. Consequently, since by Lemma 4.2 {μ0N} satisfies the O(Nd)-entropy assumption, by (41) for some constant C0 for all γ<γ0

H¯L([0,T])(1+1γ)C+Za(ρ)L([0,T]×Td)+1γlogZ(Φ(a))+1Z(Φ(a))<+,

establishing the claim of Lemma 4.3.

The bound (36) on the entropy production can be estimated explicitly. Since νρt(·)N, νaN are product measures, ψt can be computed explicitly. Then by differentiating, using the chain rule, the fact that ρ is a solution of the hydrodynamic equation, the relations φiiZ(φ)Z(φ)=Ri(φ), i=1,2 and the relation (13) we obtain

tψtNψtN=xTNdΔΦ(ρt(x/N))Φ(ρt(x/N)),DΦ(ρt(x/N))[η(x)-ρt(x/N)]. 43

We note here that as in the asymmetric case treated in [16], at this point of the application of the relative entropy method for two-species ZRPs one has to use the macroscopic analogue (13) of the compatibility relations (6).

For the other term, by computations of the action of the generator on ψtN similar to the ones for the single-species case in [19],

LNψtNψtN=i=1,2x,yTNd[Φi(ρt(y/N))Φi(ρt(x/N))-1][gi(η(x))-Φi(ρt(x/N))]p(y-x). 44

Since Φ(ρt) is C2+θ for some θ>0 and the n.n. transition probability has mean zero, the Taylor expansion for C2+θ functions yields (with the renormalisation p(Zd)=2d) that

N2LNψtNψtN=xTNdΔ[Φ(ρt)]Φ(ρt)xN,g(η(x))-Φ(ρt(x/N))+rN(t). 45

Here, for any T[0,Tmax), the remainder rN(t) satisfies the bound

|rN(t)|CTgNθ|η|1+CTMTmTNd-θ

for all t[0,T], where g is the constant in (4), CT=C(d,p,Φ(ρ),T)0 is the constant

CT=dsup0tTD2[Φ1(ρt)]CθD2[Φ2(ρt)]CθyZdy2+θp(y)

with ·Cθ denoting the θ-Hölder seminorm and

mT:=inf(t,u)[0,T]×Tdmini=1,2Φi(ρt(u))>0,MT:=sup(t,u)[0,T]×Td|Φ(ρ(t,u))|1<+.

By this bound on the remainder and the conservation of the number of particles it follows that for all t[0,T][0,Tmax), T>0,

1Nd0trN(t)dμtNdtCTgtNd+θ|η|1dμ0N+CTMTtmT1Nθ,

which according to Lemma 4.1 shows that

0trN(s)dμsNdso(Nd). 46

Since the function Δ[Φ(ρt)]Φ(ρt) is in Cloc([0,Tmax)×Td), a change of variables shows that

0txTNdΔ[Φ(ρs)]Φ(ρs)xN,η(x)-η(x)dμsNds=o(Nd) 47

for all t[0,Tmax). Integrating (36) in time, using the explicit expressions (43), (45), taking into account (46) and the fact that {μ0N} is an entropy local equilibrium (i.e., (20) holds) and using (47) and the one-block estimate, one obtains that for all t(0,Tmax)

HN(t)0txTNdΔ[Φ(ρs)]Φ(ρs)xN,Ψ(ρs(x/N),η(x))dμsNds+o(Nd), 48

where Ψ:R(DRo)×R+2R2 is the quasi-potential

Ψ(ρ,λ)=Φ¯(λ)-Φ(ρ)-DΦ(ρ)(λ-ρ) 49

and the term o(Nd) satisfies o(Nd)/Nd0 as N and then tend to infinity. In the definition of the quasi-potential the second variable λ is in R+2 since it is to be substituted by the large microscopic averages η(x), xTNd. Thus the extension Φ¯ of Φ must be used in the quasi-potential. To simplify the notation, we set

Gt(u,λ):=Δ[Φ(ρt)]Φ(ρt)(u),Ψ(ρt(u),λ). 50

By the relative entropy inequality, we have for all γ>0 and all 0s<Tmax that

xTNdGs(x/N,η(x))dμsN1γHN(s)+1γlogeγxTNdGs(xN,η(x))dνρs(·)N.

By combining this inequality with the bound (48), dividing by Nd and taking the lim sup as N and then , we get

H(t)1γ0tH(s)ds+lim sup,N+1γNd0tlogeγxTNdGs(xN,η(x))dνρs(·)Nds, 51

where in order to obtain the term 0tH(s)ds we used Lemma 4.3 to pass the limit inside the integral and lim sup,N+ denotes the lim sup as N+ and then +.

To complete the proof of Theorem 3.2, it remains to show that for each t[0,Tmax) we can choose γ>0 small enough so that the rightmost term in (51) vanishes. We begin by noting that the function G:[0,Tmax)×Td×R+2R defined in (50) satisfies

|Gt(u,λ)||Δ[Φ(ρt)]Φ(ρt)(u)|{g(|λ|1+|(ρt(u))|1)+|DΦ(ρt(u))|(|λ|1+|ρt(u)|1)}

for all (t,u,λ)[0,Tmax)×Td×R+2, which for any t[0,Tmax) yields the inequality

sup(s,u)[0,t]×Td|Gs(u,λ)|Ct·(1+|λ|1)for allλR+2 52

for some constant Ct<+. Since for any t[0,Tmax) we have ρ([0,t]×Td)R(DRo) the set Φ(ρ)([0,T]×Td) is bounded away from the critical densities φcDZ, and thus there exists ε>0 such that

sup(t,u)[0,T]×TdΛρ(t,u)(λ)<+,λD(0,ε),

i.e., 0(Dsup(t,u)[0,T]×TdΛρ(t,u))o=((t,u)[0,T]×TdDΛρ(t,u))o. It follows that by choosing γt small enough so that γtCt<ε, we can pass the limit superior as N+ and then + inside the time integral in the rightmost term in (51). Thus in order to complete the proof it remains to show that for each t[0,Tmax) we can choose γt>0 small enough so that

lim sup,N+1γtNdlogeγtxTNdGt(xN,η(x))dνρt(·)N0. 53

The proof of (53) relies on a corollary of the Laplace-Varadhan lemma [4, Sect. 4.3] for the large deviations principle satisfied by the independent family of the occupation variables {η(x)}xZd with respect to the invariant measure νρ on the infinite lattice Zd for some ρA. Since the one-site marginal νρ1 has some exponential moments for ρA, by Cramér’s theorem, the large deviations functional of the family {η(x)}xZd is given by the Legendre transform Λρ of the logarithmic moment-generating functional Λρ. Note that (15) implies that modulo an affine function depending on ρ, the rate functional Λρ coincides with the thermodynamic entropy S, that is

Λρ(λ)=S(λ)-λ,logΦ(ρ)+logZ(Φ(ρ)). 54

Lemma 4.4

Let ρ:TdR(DRo) be a continuous profile and let G:Td×R+R be a continuous function such that

supuTd|G(u,λ)|C(1+|λ|1)for allλR+2 55

for some constant C>0 such that (2C,2C)(uTdDΛρ(u))o. Then

lim suplim supN1NdlogexTNdG(xN,η(x))dνρ(·)NTdsupλR+2{G(u,λ)-12Λρ(u)(λ)}du.

We omit the proof of this Lemma as it is a simple adaptation of the corresponding result in the one-species case, [19, Lemma 6.1.10]. By the bound (52) the function G:[0,Tmax)×Td×R+2R defined in (50) satisfies

supuTd|Gt(u,λ)|Ct(1+|λ|1)

for each fixed t[0,Tmax). Therefore, if we choose γt>0 small enough so that 2γtCt(e1+e2)(uTdΛρt(u))o, then for all γ(0,γt) the function γGt satisfies the assumptions of Lemma 4.4, and thus for γ(0,γt) the term in (51) is bounded above by

TdsupλR+2{γGt(u,λ)-12Λρt(u)(λ)}du. 56

To complete the application of the relative entropy method, it remains to show that by reducing γt>0, t[0,Tmax), if necessary, this last term is non-positive.

We note that this would follow if we had a bound of the form

Bt:=supρKtλR+2|Ψ(ρ,λ)|Λρ(λ)<+, 57

where KtA:=R(DRo)(0,)2 is a compact set containing the image ρt(Td). Indeed, since Λρ(λ)=0 iff λ=ρ, in which case Ψ(ρ,λ)=0, we would then have that

|Ψ(ρ,λ)|BtΛρ(λ)for all(ρ,λ)Kt×R+2,

and so for γ(0,γt) we would have

γ|Gt(u,λ)|γΔ[Φ(ρt)]Φ(ρt)L(Td;2)BtΛρt(u)(λ)

for all (u,λ)Td×R+2. Then by choosing γt>0 small enough so that in addition γtBtΔ[Φ(ρt)]/Φ(ρt)L(Td;2)<12, it would follow that (56) is non-positive, and the proof would be complete. The bound (57) is proved in Lemma 4.5. Before we proceed with the proof of Lemma 4.5, we recall some facts on recession functions of convex functions.

Given a lower semicontinuous proper convex function ψ:Rd(-,+] with 0Dψ, its recession function ψ:Rd(-,+] is defined by

ψ(y):=limt+ψ(ty)t=limt+ddt|+ψ(ty),

where ddt|+ denotes differentiation from the right. The recession function ψ is obviously positively 1-homogeneous, ψ(λy)=λψ(y) for all yRd, λ0.

It is well known [22, Theorem 8.5] that if ψ is a proper lower semi-continuous convex function, then so is its recession function. Using the equivalent definition of recession functions via the recession cone of their epigraphs [22, Sect. 8], one can express the recession function by the formula

ψ(y)=inf{lim infk+ψ(tkyk)tk|tk+,yky} 58

(see [10, (12.7.1)]). Particularly useful in the proof of the following lemma is the characterisation of the interior of the proper domain of a convex function ψ via the recession function of its Legendre transform, as stated in [10, (12.7.3)],

Dψo=y0{xRd|x,y<(ψ)(y)}. 59

Applying (59) to the thermodynamic pressure P:=logZ, Z:=Zexp, we get

log(DZo(0,)2)=DZo={μR2|S(λ)>λ,μ,λ0}. 60

In other words, DZo is the intersection of all hyperplanes {μR2|μ,υ<S(υ)} for υS1(0,)2. This implies that the function S1(0,)2υS(υ)υR2 is a parametrisation of the boundary DZ. This may be compared with [13, (2.14)]. Consequently, the part of the boundary DZ on the strictly positive quadrant is given by the parametrisation eS(υ)υ, υS1(0,)2. Along the two axes φ1=0 and φ2=0, there is only one-species of particles and the critical fugacities in these directions are fugacities of one species ZRPs.

Lemma 4.5

For any compact KA:=R(DRo)(0,)2,

sup(ρ,λ)K×R+2|Ψ(ρ,λ)|Λρ(λ)<+. 61

Proof

For all (ρ,λ)K×(0,)2 we have that Λ(ρ,λ):=Λρ(λ)0 and the functions |Ψ|:K×(0,)2R+ and Λ:K×(0,)2R+ are continuous. Therefore the fraction in the supremum can tend to infinity if the nominator goes to infinity or the denominator goes to zero. Since Ψ:K×(0,)2R2 is continuous and K is compact the nominator can tend to infinity only as |λ|1+. In this case Λρ also tends to + as a rate functional with compact level sets. Since Λρ is the rate functional of the i.i.d. occupation variables η(x), xZd, with common law νρ1 we have that Λ(ρ,λ)=0 iff ρ=λ for the denominator. But obviously for ρ=λ we have Ψ(ρ,λ)=0, so the nominator vanishes as well. So in order to prove the lemma we have to show that the nominator and the denominator are of the same order as |ρ-λ|0 and |ρ-λ|+.

Motivated by the previous sketch, we choose ε>0 such that Kε:=K(ε)¯A, where K(ε):=xKD(x,ε), and for any M>0 we separate the region K×(0,)2 as K×(0,)2=E0εEεMEM, where

E0ε:={(ρ,λ)K×(0,)2||ρ-λ|ε},EεM:={(ρ,λ)K×(0,)2|ε|ρ-λ|M},EM:={(ρ,λ)K×(0,)2||ρ-λ|M}.

We prove the claim on each region individually. Obviously the set EεM is compact and so since the functions Ψ and Λ are jointly continuous, the claim holds on the region EεM.

We turn to the region E0ε. By its definition, for any (ρ,λ)E0ε we have that λD(ρ,ε)KεA. So, since D(ρ,ε) is convex, for all (ρ,λ)E0ε the image of the constant speed line segment γρ,λ:[0,1]R2 from ρ to λ is contained in Kε, i.e.,

γρ,λ([0,1])Kεfor all(ρ,λ)E0ε. 62

By the first order Taylor expansion of Φi, i=1,2 around the point ρK,

Ψi(ρ,λ)=01(1-t)λ-ρ,D2Φi(γρ,λ(t))(λ-ρ)dtfor all(ρ,λ)E0ε.

Since Φ is smooth on the set A, the matrix D2Φi(ρ) is symmetric for all ρA. Denoting by λ±i(ρ) the real eigenvalues of D2Φi(ρ) we have

λ-i(γρ,λ(t))|λ-ρ|2λ-ρ,D2Φi(γρ,λ(t))(λ-ρ)λ+i(γρ,λ(t))|λ-ρ|2.

Furthermore, by the continuity of the eigenvalues λ±i as functions of ρA,

Ai:=supρKε|λ-i||λ+i|(ρ)<+.

So by (62), we have that |λ-i||λ+i|(γρ,λ(t))Ai for all (t,ρ,λ)[0,1]×E0ε and thus

|Ψi(ρ,λ)|Ai2|λ-ρ|2,i=1,2.

For the denominator in (61), we note that the rate functional Λρ is C1 on (0,)2 and C2 on A with

Λρ(λ)=logΦ¯(λ)Φ(ρ),λ(0,)2,
D2Λρ(λ)=DlogΦ(λ)=D2S(λ),λA,

where S is the thermodynamic entropy. Since Λρ and its derivative vanish at ρ, by Taylor expansion of Λρ around ρK

Λρ(λ)=01(1-t)λ-ρ,D2S(γρ,λ(t))(λ-ρ)dt,λA.

Denoting by λ-(ρ)>0 the minimal eigenvalue of the strictly positive definite matrix D2S(ρ), we have by continuity that

B:=infρKελ-(ρ)>0.

Then Λρ(λ)B2|λ-ρ|2 for all (ρ,λ)E0ε, which shows that

sup(ρ,λ)E0ε|Ψi(ρ,λ)|Λρ(λ)AiB<+,i=1,2

and yields the bound (61) in the region E0ε.

It remains to show that the supremum is finite in the region EM for some M>0. On one hand, it follows from (16) and the compactness of K that Ψ satisfies a bound of the form

|Ψ(ρ,λ)|1C0+C1|λ|1(ρ,λ)K×R+2

for some constants C0,C10. So, to complete the proof, it suffices to show that Λ has at least linear growth in EM as |λ|+, i.e.,

limM+inf(ρ,λ)EMΛρ(λ)|λ|>0,

where of course the limit as M+ exists as an increasing limit. We begin by noting that

limM+inf(ρ,λ)EMΛρ(λ)|λ|lim inf|λ|+infρKΛρ(λ)|λ|=:a.

We choose a sequence {λn}R+2 achieving the limit inferior,

|λn|+andlimn+infρKΛρ(λn)|λn|=a.

Since {λn|λn|} is contained in the compact space S+1:=S1R+2, by passing to a subsequence if necessary, we can assume that {λn|λn|} converges to some direction υS+1. Then obviously

lim infn+S(λn)|λn|lim inf|λ|+λ/|λ|υS(λ)|λ|=S(υ), 63

where the equality in the right-hand side holds by (58). Since Φ(K)DZo(0,)2, we have by (60) that S(υ)-υ,logΦ(ρ)>0 for all ρK. Thus, since Φ is continuous and K is compact,

θ:=infρK{S(υ)-υ,logΦ(ρ)}>0.

Then by (63) there exists n1N such that

nn1S(λn)|λn|S(υ)-θ3.

By (54) and taking into account the fact that Z1, we have that for all nn1 and all ρK,

Λρ(λn)|λn|S(υ)-λn|λn|,logΦ(ρ)+1|λn|logZ(Φ(ρ))-θ3S(υ)-λn|λn|,logΦ(ρ)-θ3.

But by the compactness of K, we have that logΦL(K):=supρK|logΦ(ρ)|2<+ and therefore the sequence {λn|λn|,logΦ(ρ)} converges to υ,logΦ(ρ) uniformly over all ρK,

supρK|λn|λn|,logΦ(ρ)-υ,logΦ(ρ)|logΦL(K)|λn|λn|-υ|20.

Therefore we can choose n2N such that

nn2supρK|λn|λn|,logΦ(ρ)-υ,logΦ(ρ)|<θ3,

and then for all nn1n2 and all ρK

Λρ(λn)|λn|S(υ)-υ,logΦ(ρ)-2θ3θ-2θ3=θ3>0.

This proves that

lim inf|λ|+infρKΛρ(λ)|λ|=limn+infρKΛρ(λn)|λn|>0,

which completes the proof of Lemma 4.5.

Since Lemma 4.5 establishes the missing bound (57), the proof of Theorem 3.2 is complete.

Proof of Theorem 3.3

By [1], it is known that quasilinear parabolic systems have unique maximal classical solutions when starting from initial profiles of class C2+θ, θ[0,1). To show that classical solutions of the species-blind parabolic system (26) are global in time, we prove first a maximum principle asserting that the region

A:=R(DRo)(0,)2={ρ(0,)2|ρ1+ρ2<ρ^c}

is invariant under the evolution of the species-blind parabolic system. Here ρ^c(0,+] is the critical density of the one-species ZRP associated with the species-blind ZRP. The proof of this version of the maximum principle for systems of the form (26) relies on the maximum principle for quasilinear PDEs in divergence form found in [2]. Since, as we will see, the solution ρ cannot lose regularity, we will obtain the existence of global in time classical solutions.

Lemma 4.6

(A maximum principle for the species-blind parabolic system) Let ρ=(ρ1,ρ2)C1,2([0,T)×Td;R2), T>0, be a classical solution of the species-blind parabolic system (26) starting from an initial condition ρ0C2(Td;R+2) satisfying

ρ0(Td)A={ρ(0,)2|ρ1+ρ2<ρ^c}, 64

where ρ^c is the critical density corresponding to the one-species density function R^. Then

0<inf(t,u)[0;T)×Tdρ1(t,u)ρ2(t,u)sup(t,u)[0,T)×Td(ρ1(t,u)+ρ2(t,u))supuTd(ρ1(0,u)+ρ2(0,u))<ρ^c. 65

Proof

By the continuity of ρ0 and the compactness of Td, there exists by assumption (64) an ε>0 such that

ρ0(Td){(ρ1,ρ2)R2|ρ1ρ2>ε,ρ1+ρ2<ρ^c-ε}, 66

where we replace ρ^c-ε by 1ε when ρ^c=+. Since ρ solves (26), by summing the two equations we see that the function ρ1+ρ2 solves the equation tρ=ΔΦ^(ρ). But since Φ^ is the mean jump rate of a single species ZRP,

0<c<Φ^(ρ)<C<+for allρ[0,ρ^c-ε/2] 67

for some constants c,C0 and therefore the equation tρ=ΔΦ^(ρ) is uniformly parabolic, when considered for sub-critical initial conditions ρ0C(Td,(0,ρ^c)). Therefore it follows by (66) and the maximum principle for scalar uniformly parabolic quasilinear equations that

2ε<inf(t,u)[0;T)×Td(ρ1+ρ2)(t,u)sup(t,u)[0;T)×Td(ρ1+ρ2)(t,u)<ρ^c-ε. 68

We consider now the family of the open domains

Bδ:={(ρ1,ρ2)R2|ε<ρ1+ρ2<ρ^c-ε,ρ1ρ2>-δ}

for δ[0,+] and set

Dδ:={(t,u,r)[0,T)×Td×R|(r,ρ2(t,u))Bδ}.

Let Ψ:DR denote the function given by the formula

Ψ(t,u,r)=rΦ^(r+ρ2(t,u))r+ρ2(t,u).

The sets Dδ are obviously open and the function Ψ is well defined on D. Since the sum ρ1+ρ2 satisfies (68), we have that

(t,u,ρ1(t,u))Dfor all(t,u)[0,T)×Td,

and since (ρ1,ρ2) is a solution of (26), we have that ρ1 solves

tρ1(t,u)=ΔΨ(t,u,ρ1(t,u)).

In divergence form, the problem above is written as

tρ1(t,u)=divAΨ(t,u,ρ1(t,u),ρ1(t,u)) 69

where AΨ:DRd is the function given by the formula

AΨ(t,u,r,υ)=uΨ(t,u,r)+rΨ(t,u,r)υ.

Since ρ2 is C1,2, it follows that the function AΨ is C1 and υAΨ(t,u,r,υ)=rΨ(t,u,r)I where IRd×d denotes the identity matrix. By a simple calculation, rΨ(t,u,r)=H(r,ρ2(t,u)), where H:BR is given by

H(ρ1,ρ2)=ρ2ρ1+ρ2Φ^(ρ1+ρ2)ρ1+ρ2+ρ1ρ1+ρ2Φ^(ρ1+ρ2).

We have that

infBδHinfDδrΨsupDδrΨsupBδH 70

for all δ[0,+] and it is obvious that

cinfB0HsupB0HC,

where c,C0 are the constants in (67). By continuity of H, we obtain the existence of δ0>0 such that

c2<infBδ0HsupBδ0H<2C, 71

which shows that the diagonal matrix υAΨ is positive definite on the set Dδ0×Rd. We set now

Ti:=sup{t[0,T]|inf(s,u)[0,t)×Tdρi(s,u)>0},i=1,2.

By the assumptions on the initial condition ρ0, the set over which we take the supremum is non-empty. By the continuity of the solution ρ, we have Ti>0 for i=1,2 and if Ti<T then there exists u0iTd such that ρi(Ti,u0i)=0. In order to prove the claim of the lemma, it suffices to show that T1=T2=T.

So we suppose that this is not true to obtain a contradiction. Without loss of generality it suffices to consider the cases T1<T2<T and T0:=T1=T2<T.

  1. T1<T2<T: Since ρ1(t,u)0 for all (t,u)[0,T1]×Td and ρ1 is continuous in [0,T)×Td, there exists t0>0 such that
    inf(t,u)[0,T1+t0]×Tdρ1(t,u)>-δ0.
    But then (t,u,ρ1(t;u))Dδ0 for all (t,u)[0,T1+t0]×Td and so, since ρ1 and 0 are solutions of problem (69) in [0,T1+t0]×Td, which is uniformly parabolic in this region by (70) and (71), and since ρ1(T1,u01)=0, we get from [2, Theorem 1] that ρ10 in [0,T1)×Td, which contradicts the definition of T1.
  2. T0:=T1=T2<T: Again, since ρ1(t,u)ρ2(t,u)>0 for all (t,u)[0,T0]×Td, there exists t0>0 such that
    inf(t,u)[0,T1+t0]×Td[ρ1(t,u)ρ2(t,u)]-δ0.
    But then again the problem (69) is uniformly parabolic in [0,T0+t0]×Td and ρ1 and 0 are solutions with ρ10 in [0,T0], which again by [2, Theorem 1] yields ρ10 in [0,T0)×Td and contradicts the definition of T0.

Using this maximum principle and the global existence of scalar uniformly parabolic equations, we obtain the global existence of solutions to the species-blind parabolic system as follows. To derive a contradiction, we assume that ρC1,2([0,Tmax)×Td;R2), Tmax<+, is the maximal classical solution of the species-blind parabolic system starting from ρ0C2+θ(Td). Here maximality of the solution means that ρ can not be extended to a C1,2-solution on [0,T)×Td for T>Tmax. Since ρ^0:=ρ01+ρ02C1+θ;2+θ(Td;(0,ρc)), there exists a unique solution ρ^C1+θ,2+θ(R+×Td;(0,ρc)) of the scalar quasilinear parabolic equation tρ=ΔΦ^(ρ) with initial data ρ^0. Then, ρ^(R+×Td)(ε,ρ^c-ε) for some ε>0 and the function ϕ(x):=Φ^(x)x is C in [ε,ρ^c-ε]. Thus the function a:R+×TdR+ defined by a(t,u):=Φ^(ρ^(t,u))ρ^(t,u) belongs to C1+θ,2+θ(R+×Td). Since Φ^ satisfies (67),

0<c<a(t,u)C<+for all(t,u)R+×Td 72

for some constants c,C0. Since the function ρ1+ρ2 is also a solution of the scalar equation tρ=ΔΦ^(ρ) with the same initial data ρ0, we have by the uniqueness of solutions that

aΦ^(ρ1+ρ2)ρ1+ρ2in[0,Tmax)×Td. 73

We consider the system

tρ1=Δ(a(t,u)ρ1(t,u))tρ2=Δ(a(t,u)ρ2(t,u)),ρ(0,·)=(ρ01,ρ02)inTd, 74

which is obviously decoupled and can be solved by solving the scalar linear second order parabolic equation

tρ=Δ(a(t,u)ρ(t,u)) 75

twice with initial conditions ρ01 and ρ02. This scalar equation is given in general form by

tρ=i,j=1daijij2ρ+i=1dbiiρ+cρ,

where aij=aδij, bi=ia and c=Δa. We note that since a satisfies (72) and aij=aδij, the matrix (aij) is uniformly elliptic. Also, since aC1+θ,2+θ(R+×Td), the coefficients aij,bi,c are θ-Hölder continuous and so by the interpretation of [20, Theorem 5.14] in the flat torus with periodic boundary conditions, we find that for any ρ0C2+θ(Td) there exists a unique solution ρCloc1+θ,2+θ(R+×Td) to the scalar problem (75) with initial condition ρ0, and thus there exists a unique solution ρ~Cloc1+θ,2+θ(R+×Td;R2) of system (74) starting from ρ0=(ρ01,ρ02). Since by (73), we have that the solution ρC1,2([0,Tmax)×Td;R2) of the system (26) also solves the system (74), it follows by the uniqueness of solutions that ρ~=ρ in [0,Tmax)×Td. This, taking also into account the maximum principle, shows that

ρC1+θ,2+θ([0,Tmax)×Td;A).

Now, we obviously have that ρ~TmaxC2+θ(Td), and since ρ~ solves (26) in [0,Tmax)×Td, we have by the maximum principle that

ρ~([0,Tmax)×Td){rA|d(r,A)>δ}

for some δ>0. Consequently, by continuity, we also have that ρ~Tmax(Td)A. We consider then a solution r:[0,ε)×TdA, ε>0, of the problem (26) starting from r0=ρ~Tmax and extend ρ on [0,Tmax+ε)×Td by defining ρ(t,·):=r(t-Tmax,·) for t[Tmax,Tmax+ε). This function is obviously of class C1+θ,2+θ and solves (26), which contradicts the maximality of Tmax.

Proof of Corollary 3.1

By the global existence in time of solutions to the species-blind parabolic system, it suffices to check that Theorem 3.2 applies. Since the the one-species partition function Z^ is continuous on DZ^, it follows by the formula Z(φ)=Z^(φ1+φ2) that the partition function is continuous. It remains to check that in the case where the associated one-species ZRP has finite critical density, g has regular tails, i.e., that for every υS1,+1

μc;1(υ):=logφc;1(υ):=lim inf|k|1+k/|k|1υ1|k|1logg!(k),υS1,+1 76

exists as a limit and is a continuous function of the direction υS1,+1. By the formula of g! we have that

1|k|1logg!(k)=1|k|1logk1!k2!|k|1!+1|k|1logg^!(|k|1). 77

The second term in the right hand side of (77) converges as |k|1+ to the critical chemical potential μ^c=logφ^c of the one-species jump rate g^. Since by Stirling’s approximation limk+k!2πk(k/e)k=1, we can replace the liminf of the first term in the right hand side of (77) by

lim inf|k|1+k/|k|1υ1|k|1log2πk1k1k1k2k2k2|k|1|k|1|k|1. 78

This limit inferior exists as a limit and defines a continuous function of υ. Indeed, for all kN2 we have that

1|k|1logk1k1k1k2k2k2|k|1|k|1|k|1=1|k|1logk1k2|k|1+log(k1|k|1)k1|k|1+log(k2|k|1)k2|k|1,

and it is easy to check that lim|k|+1|k|1logk1k2|k|1=0, so that

μc;1(υ)=lim|k|1+k/|k|1υk1,k2>0[log(k1|k|1)k1|k|1+log(k2|k|1)k2|k|1+logg!(|k|1)1|k|1]=υ,logυ+μc,

with the convention υilogυi=0 if υi=0 since xlogx0 as x0. Finally, points kN02 with ki=0 for some i=1,2 contribute to the limit only if υ=ei for some i=1,2. For such points kN02, we have k1!k2!=|k|1!, and so the first term in the right hand side of (77) vanishes, which agrees with the fact that υ,logυ=0 if υ=ei, i=1,2. This is to be expected, since in the directions υ=ei with i=1,2 in the phase space we have only one of the two species of particles, which when on their own perform the underlying one-species ZRP with critical chemical potential μ^c=logφ^c. This completes the proof that g has regular tails.

Acknowledgements

All authors thank the Leverhulme Trust for its support via Grant RPG-2013-261. JZ gratefully acknowledges funding by the EPSRC through project EP/K027743/1 and a Royal Society Wolfson Research Merit Award. ND gratefully acknowledges funding by the EPSRC through project EP/M028607/1. We also thank the anonymous reviewers for their very careful reading and numerous comments which improved the manuscript.

Contributor Information

Nicolas Dirr, Email: DirrNP@cardiff.ac.uk.

Marios G. Stamatakis, Email: zimmer@maths.bath.ac.uk

Johannes Zimmer, Email: M.G.Stamatakis@bath.ac.uk, Email: ma.ge.stams@gmail.com.

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