Contact process on a dynamical long range percolation M. SeilerA. Sturm

2025-05-02 0 0 868.89KB 31 页 10玖币
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Contact process on a dynamical long
range percolation
M. SeilerA. Sturm
November 27, 2023
In this paper we introduce a contact process on a dynamical long range percolation
(CPDLP) defined on a complete graph (
V, E
). A dynamical long range percolation is a
Feller process defined on the edge set
E
, which assigns to each edge the state of being
open or closed independently. The state of an edge
e
is updated at rate
ve
and is open
after the update with probability
pe
and closed otherwise. The contact process is then
defined on top of this evolving random environment using only open edges for infection
while recovery is independent of the background. First, we conclude that an upper
invariant law exists and that the phase transitions of survival and non-triviality of the
upper invariant coincide. We then formulate a comparison with a contact process with
a specific infection kernel which acts as a lower bound. Thus, we obtain an upper bound
for the critical infection rate. We also show that if the probability that an edge is open is
low for all edges then the CPDLP enters an immunization phase, i.e. it will not survive
regardless of the value of the infection rate. Furthermore, we show that on
V
=
Z
and under suitable conditions on the rates of the dynamical long range percolation the
CPDLP will almost surely die out if the update speed converges to zero for any given
infection rate λ.
Keywords Contact process, evolving random environment, dynamical random graphs, interacting
particle systems, long range percolation
1 Introduction
The classical contact process on a fixed graph describes the spread of an infection over time and
space. It has been studied intensively and many variations have been considered, see Section 3.1 for
more background. In this article we study a contact processes on a dynamical long range percolation
(CPDLP), in which infections over any distance are possible depending on whether the corresponding
edge is present, which also changes dynamically.
We assume that the underlying graph
G
= (
V, E
) is a connected and transitive graph with
bounded degree. The graph distance of
G
is denoted by
d
(
·,·
) and the set of all possible edges by
E
:=
{e
=
{x, y}
:
x, y V, x ̸
=
y}
. From now on we consider the complete graph (
V, E
) which we
also equip with the original graph distance d(·,·).
There are several notions of transitivity for graphs in the literature. Thus, we specify the notion
briefly. Here a graph
G
is called transitive if for any pair of vertices
x1, x2V
and respectively for
any pair of edges
e1, e2E
, there exists a graph automorphism
ϕ
which maps
x1
to
x2
and
e1
to
e2
.
A graph automorphism is a permutation on
V
which preserves the graph structure, i.e.
{x, y} ∈ E
iff {ϕ(x), ϕ(y)} ∈ E. In the literature this is sometimes called vertex and edge transitivity.
The CPDLP (C
,
B) = (C
t,
B
t
)
t0
is a Markov process on
P
(
V
)
× P
(
E
), where
P
(
V
) and
P
(
E
)
denote the power sets of
V
and
E
. We equip the space
P
(
V
)
× P
(
E
) with the topology induced
Frankfurt Institute for Advanced Studies, Ruth-Moufang-Straße 1, 60438 Frankfurt am Main, Germany
E-mail: seiler@fias.uni-frankfurt.de
Institute for Mathematical Stochastics, Georg-August-Universit¨at G¨ottingen, Goldschmidtstr. 7, 37077
ottingen, Germany E-mail: anja.sturm@mathematik.uni-goettingen.de
1
arXiv:2210.08907v2 [math.PR] 23 Nov 2023
by pointwise convergence, i.e. (
Cn, Bn
)
∈ P
(
V
)
× P
(
E
) converges to (
C, B
) if
1{(x,e)(Cn,Bn)}
1{(x,e)(C,B)}
for all (
x, e
)
∈ P
(
V
)
×P
(
E
)
.
Note that
P
(
V
)
×P
(
E
) is a partially ordered space with
respect to “
”. Furthermore, we denote by “
” weak convergence of probability measures on
P(V)× P(E). As usual we denote by |A|the cardinality of a set A.
We call Cthe infection process, which takes values in
P
(
V
). If
x
C
t
then we call
x
infected at
time
t
. The process Bdescribes an evolving edge random environment and takes values in
P
(
E
).
Thus, we call Bthe background process. If
e
B
t
we call
e
open at time
t
and closed otherwise.
Furthermore, we assume that Bevolves autonomously of C. Given that Bis currently in state
B
the transitions of the infection process Ccurrently in state Care for all xV,
CC∪ {x}at rate λ· |{yC:{x, y} ∈ B}| and
CC\{x}at rate r, (1)
where
λ >
0 denotes the infection rate and
r >
0 the recovery rate. We write C=C
C
when C
0
=
C.
For the background dynamics we consider a dynamical long range percolation. Let (
ˆpe
)
e∈E
[0
,
1]
and (
ˆve
)
e∈E
(0
,
) be sequences of real numbers such that
ˆp{x,y}
=
ˆp{x,y}
and
ˆv{x,y}
=
ˆv{x,y}
if
d
(
x, y
) =
d
(
x, y
). We exclude the trivial case that
ˆpe
= 0 for all
e∈ E.
Now the dynamical long
range percolation Bcurrently in state Bhas transitions
BB∪ {e}at rate ˆveˆpeand
BB\{e}at rate ˆve(1 ˆpe)(2)
for all
e∈ E
. As initial distribution we choose B
0π
, where
π
is the invariant law of Bwhich
means that the events ({eBt})e∈E are independent and P(eBt) = ˆpefor all e∈ E and t0.
We will in particular be interested in the behavior of our process when we scale the percolation
and speed kernels. For this we will assume that they are of the form
ˆpe= ˆpe(q) := qpeand ˆve= ˆve(γ) := γve(3)
for all
e∈ E
for some
γ >
0 and
q
(0
,
1] and fixed kernels (
pe
)
e∈E
[0
,
1] and (
ve
)
e∈E
(0
,
).
A long range percolation model assigns to every edge
e∈ E
independently the state of being open
with probability
ˆpe
and otherwise closed. The term ”dynamical” means that we update the state
of every edge
e
as time evolves. This is done independently for every edge
e
=
{x, y}
at update
speed ˆvewhich depends only on the length d(x, y) of that edge. This yields a translation invariant
background dynamic, where we use that the graph Gis transitive.
Since we are in a long range setting we need some assumptions regarding the flip rates of the
background process to ensure that the CPDLP is well-defined.
In order to ensure that the transition rates of the infection process are not infinite we need that
at any given time
t
the neighborhood of any vertex
x
remains finite. Therefore, we assume that the
sequence (ˆpe)e∈E and (ˆve)e∈E satisfy
X
yV\{x}
ˆv{x,y}ˆp{x,y}<and X
yV\{x}
ˆv1
{x,y}<for all xV. (4)
Note that if the kernels are of the form (3) then (
pe
)
e∈E
[0
,
1] and (
ve
)
e∈E
(0
,
) satisfy these
assumptions iff (ˆpe)e∈E [0,1] and (ˆve)e∈E (0,) do.
Remark 1.1. The assumptions in (4) imply that
ˆv{x,y}ˆp{x,y}
0 and
ˆv{x,y}→ ∞
as
d
(
x, y
)
→ ∞
.
Since we also have that
ˆve>
0 for all
e∈ E
it follows that
C
:=
infy:y̸=xˆv{x,y}>
0, where
C
does
not depend on the choice of
xV
due to translation invariance. This implies together with
(4)
that
0< C X
yV\{x}
ˆp{x,y}X
yV\{x}
ˆv{x,y}ˆp{x,y}<,
i.e. that the sequence (ˆp{x,y})yV\{x}is summable.
Thus, as a consequence of the assumptions in (4) the probability that a long edge is open, i.e. an
edge connecting two vertices over a long distance, becomes exceedingly small. Broadly speaking
this means that a successful infection over a long distance is getting more and more unlikely as
the distance increases. The second part of the assumption can be seen as assuming that all edges
attached to an arbitrary vertex are updated after a finite time. This might seem a bit unintuitive,
2
but we need this assumption for technical reasons. We discuss the necessity of this rate assumption
briefly in Section 3 right after Problem 3.
In Section 5 we will explicitly construct the CPDLP via a graphical representation and then
show that under these assumptions the resulting process is in fact a well-defined Feller process (see
Proposition 5.7) with state space
P
(
V
)
× P
(
E
) and that
|
C
t|<
almost surely for all
t
0 if
|C0|<, even if the background is started in E(see Proposition 5.6).
We are interested in the survival behavior of the CPDLP as the parameter
λ
varies, and later on
also as
γ >
0 and
q
(0
,
1) vary for percolation and speed kernels of the form (3). In the general
setting, we denote by
θ(λ, C) := P(CC
t̸=∅ ∀t0)
the survival probability of a CPDLP with infection parameter
λ
and initial state C
0
=
C
and B
0π
(and all other parameters fixed).
We denote the critical infection rate for survival by
λc:= inf{λ0 : θ(λ, {x})>0},
where
xV
is chosen arbitrary. Note that by translation invariance it follows that
θ
(
λ, {x}
) =
θ
(
λ, {y}
) for all
x, y V
. Furthermore, this together with the additivity of the infection process C
implies that
θ
(
λ, C
)
>
0 for some
CV
with 0
<|C|<
then this is true for all such sets. Thus,
the definition of the critical rate
λc
does not depend on the choice of the set of initially infected
vertices as long as it is finite and non-empty.
Furthermore, by standard methods and using the monotonicity of the system, see also Remark 5.3,
we get the existence of the upper invariant law
ν
, which is the weak limit of the process started
with (C
0,
B
0
) = (
V, E
). (Whenever relevant we will indicate the dependence of
ν
on the parameters
of the model with subscripts.) The upper invariant law is the largest invariant law according to
the stochastic order, i.e. if
ν
is an invariant law of the CPDLP, then
νν
, where ”
” denotes the
stochastic order. Of course, there exists the trivial invariant law
δπ
. This poses the question for
which parameters it holds that
ν
=
δπ
. Since it is not difficult to see that
δπ
is the smallest
invariant law possible,
ν
=
δπ
is equivalent to ergodicity of the system, i.e. that there exists a
unique invariant law which is the weak limit of the process. We define the critical infection rate for
non-triviality of the upper invariant law by
λ
c:= inf{λ > 0 : νλ̸=δπ}.
2 Main results
Our first result is that the critical infection rate of survival and the critical infection rate for a
non-trivial upper invariant law are the same.
Theorem 2.1. The two critical infection rates coincide, i.e. λ
c=λc.
The next result provides a coupling of the CPDLP with a contact process that has a general
infection kernel. As a consequence we obtain that if this contact process survives then this implies
survival of the CPDLP, and thus this leads to a sufficient criterion for a positive survival probability
of the CPLDP. We first define the contact process Xwith an infection kernel (
ae
)
e∈E
[0
,
) and
recovery rate
r >
0 on the complete graph (
V, E
). We additionally assume that
a{x,y}
=
a{x,y}
if
d(x, y) = d(x, y) and X
yV\{x}
a{x,y}<(5)
for all xV. If Xis currently in the state Cit has the transitions
CC∪ {x}at rate X
yC
a{x,y}and
CC\{x}at rate r.
(6)
This process can again be constructed via a graphical representation and it is a well known fact that
if
(5)
is satisfied then Xis a well-defined Feller process on the state space
P
(
V
), see for example
[
Lig12
, Propostion I.3.2] and [
Swa09
]. As usual we indicate the initial configuration
CV
by
adding a superscript XC, i.e. XC
0=C.
3
Theorem 2.2. Let
CV
and (C
C
t,
B
t
)
t0
be a CPDLP with parameter
λ, q
and
γ
. Then there
exists a contact process (XC
t)t0with XC
0=Cand with infection kernel
ae(λ) := 1
2λ+ ˆvep(λ+ ˆve)24λˆveˆpe0
for all e∈ E such that XC
tCC
tfor all t0. Thus, in particular
λcλc,
where
λc
:=
inf{λ >
0 :
P
(
X{x}
t̸
=
∅ ∀t
0)
>
0
}
is the critical infection rate for survival of
X
(which is again independent of xV).
The following results are concerned with the behavior of survival as we scale percolation probability
and speed with the parameters
q
and
γ
. Thus, we assume that the percolation and speed kernels are
as in (3) and consider the survival probability
θ
and the critical infection parameter
λc
as functions
of γand q.
Remark 2.3. Note that in this setting a CPDLP with rates
λ, r, γ, q
has the same dynamics as a
CPDLP with rates
λ/r,
1
, γ/r, q
when time is sped up by a factor of
r
, and the survival probabilities
are the same. Thus, the survival behavior of a CPDLP with rates
λ, r, γ, q
can be deduced from the
survival behavior of a CPDLP with rates
λ,
1
, γ, q
. In other words, it is not necessary to explicitly
study the dependence on r.
As a consequence of Theorem 2.2 we obtain the following result for fast update speed.
Corollary 2.4. Let X
be a contact process with infection kernel (
λqpe
)
e∈E
and denote the
corresponding critical infection rate by
λ
c(q) = inf{λ > 0 : Pλ,q (X{x},̸=∅ ∀t0) >0}.
Then we have
lim sup
γ→∞
λc(γ, q)lim
γ→∞ λc(γ, q) = λ
c(q)<.
The next result shows that for any fixed speed if we have overall a low probability that an edge of
any length is open, i.e. for
q
small enough, we are in the immunization region for the CPDLP. This
means that the critical infection rate is infinite and so no matter how large the infection rate is the
CPDLP will die out almost surely
Theorem 2.5. For any fixed
γ >
0there exists
q0
=
q0
(
γ
)
(0
,
1] such that Cdies out almost
surely for all
q < q0
, regardless of the choice of
λ >
0, i.e.
λc
(
γ, q
) =
for all
q < q0
, and such
that
λc
(
γ, q
)
<
for all
q > q0
. Moreover, the function
γ7→ q0
(
γ
)is monotone non-increasing on
(0,).
As a corollary we can also get more insight into the behavior of the critical infection rate
λc
(
γ, q
)
as a function of
γ
and in particular into its asymptotic behavior as
γ
0. Note that while it is clear
due to monotonicity that q7→ λc(γ, q) is a monotone non-increasing function, see also Remark 5.3,
this is not so clear for the function
γ7→ λc
(
γ, q
). Nonetheless, it can be shown (see Proposition 5.4)
that
λc
(
γ, q
) can at most increase linearly in
γ
which implies that there exists a
γ0
(
q
) such that
λc
(
γ, q
) =
for all
γ < γ0
(
q
) and
λc
(
γ, q
)
<
for all
γ > γ0
(
q
). Note that
γ0
(
q
) must be finite for
any
q >
0 due to Corollary 2.4 but that it may be 0. However, the following corollary states that for
small enough
q
we have
γ0
(
q
)
>
0 such that a nontrivial immunization phase exists. For this we now
set
q1:= sup
γ(0,)
q0(γ) = lim
γ0q0(γ),(7)
where we have used the monotonicity of
γ7→ q0
(
γ
) stated in Theorem 2.5. This means that
by Theorem 2.5 for every
q < q1
there exists a
γ >
0 such that
q < q0
(
γ
)
< q1
which implies
λc(γ, q) = and thus also γ0(q)>0. In summary, we have the following statement:
Corollary 2.6. For every
q
(0
,
1] there exists a
γ0
=
γ0
(
q
)
[0
,
)such that
λc
(
γ, q
) =
for all
γ < γ0
and
λc
(
γ, q
)
<
for all
γ > γ0
. Furthermore, there exists a
q1
(0
,
1], see
(7)
, so that for
every
q < q1
we have
γ0
(
q
)
>
0while for every
q > q1
we have
γ0
(
q
)=0
.
This implies in particular
for every q < q1that limγ0λc(γ, q) = .
4
For general countable vertex sets
V
we can only determine that
λc
(
γ, q
)
→ ∞
when
γ
0 if
q < q1
is small enough. But in the special case
V
=
Z
and
E
=
{{x, y} ⊂ Z
:
|xy|
= 1
}
, i.e. when
G
= (
V, E
) is the 1-dimensional integer lattice we can conclude that this is the case for all
q <
1
,
under some further assumptions. In fact, these assumptions even guarantee that for any fixed
λ
we
cannot have survival if the update speed γis small enough.
Theorem 2.7. Consider
G
to be the 1-dimensional integer lattice. Let
q <
1be fixed and
CV
be
non-empty and finite. Furthermore, assume that the sequences (pe)e∈E and (ve)e∈E satisfy
X
yN
yv{0,y}p{0,y}<and X
yN
yv1
{0,y}<.(8)
Then, for every
λ >
0there exists
γ
=
γ
(
λ, q
)
>
0such that C
C
dies out almost surely for all
γγ, i.e. θ(λ, γ, q, C) = 0 for all γγ. Thus, in particular limγ0λc(γ, q) = .
Note that
(8)
is a stronger assumption than
(4)
, and thus already implies the latter assumption.
2.1 Outline
The rest of this paper is organized as follows. In Section 3 we discuss some related literature in
order to put our results into context with the current state of research. Then, we state and discuss
some open problems and possible directions for future research.
Since we will use on several occasions a comparison with an independent long range percolation
model we introduce this type of model in Section 4 and state some conditions which imply the
absence of an infinite connected component.
In Section 5 we construct the CPDLP via a graphical representation. Furthermore, in Subsection 5.1
we show that this construction yields a well-defined Feller process. In Subsection 5.2 we describe the
construction of a dual infection process, which yields a self-duality relation. We then use this relation
to prove Theorem 2.1. In Subsection 5.3 we use the graphical representation to show Theorem 2.2
and Corollary 2.4.
In Section 6 we compare the dynamical long range percolation blockwise with an independent long
range percolation model and define a new infection process, which dominates the original one. We
use this newly defined process to show Theorem 2.5 in Subsection 6.1. Lastly, we show Theorem 2.7
in Subsection 6.2.
3 Discussion
3.1 Related literature
The contact process was first introduced almost half a century ago by Harris [
Har74
] on
Zd
. Since
then this process and many variations of it have been studied intensively, mostly on bounded
degree graphs. To the best of our knowledge the first to introduce a long range variation of the
contact process, where there is no intrinsic bound on the distance between two vertices for which
a transmission of an infection can take place, was Spitzer [
Spi77
]. He studied so-called nearest
particles systems. Bramson and Gray [
BG81
] studied in particular the phase transition of similar
systems. See also [Lig12, Chapter VII] for more results on nearest particles systems.
Swart [
Swa09
] studied a contact process with general infection kernel (
ae
)
e∈E
as in
(5)
and
(6)
,
see also [
AS10
], [
SS14
] and [
Swa18
] for more results on this process. For applications in certain areas
of physics, see for example [Gin+06].
Another long range variation of the model is a contact process defined on a random graph with
unbounded degree. To be precise, the considered graph has almost surely finite degree but there
exists no uniform bound for the degree of a vertex. For example, Can [
Can15
] studied a contact
process on an open cluster generated by a long range percolation, and M´enard and Singh [
MS16
]
considered the phase transition of contact processes on more general graphs of unbounded degree.
In this paper we study the spread of an infection in a dynamical random environment. To the best
of our knowledge the first to study such a model explicitly was Broman [
Bro07
] followed by Steif
and Warfheimer [
SW08
], who considered a contact process with varying recovery rates. Remenik
[
Rem08
] studied a related model and made connections to multi-type contact processes, which had
been studied earlier, see for example Durrett and Møller [DM91].
5
摘要:

ContactprocessonadynamicallongrangepercolationM.Seiler∗A.Sturm†November27,2023Inthispaperweintroduceacontactprocessonadynamicallongrangepercolation(CPDLP)definedonacompletegraph(V,E).AdynamicallongrangepercolationisaFellerprocessdefinedontheedgesetE,whichassignstoeachedgethestateofbeingopenorclosedi...

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