1.1. Model and Research Background
This paper is concerned with the spatial propagation of the nonlocal reaction-diffusion model in the cylinder domain
as follows
where
is a bounded domain in
with a smooth boundary
and
is the outward unit normal vector to
. This model can be used to study the internal competition among various phenotypes within a single population. Here
denotes the density of a population living in a continuous spatial variable
and displaying a continuous bounded phenotypical trait
, where
is the set of all possible traits. The traits represent variations within species, such as rate of food intake, average litter size, flowering time, or age at maturity. The birth rate is given by
, which takes into account the influence of natural selection on population survival. The nonlocal term
indicates that the intra-specific competition occurs among individuals with any trait
y at the location
x, and
is the competitive ability of the individual with trait
y. For more detailed biological background of (
1), we refer to [
1,
2]. Moreover, the results in ([
3] Theorem 2) showed that there is a unique solution of (
1) for any nonnegative bounded initial data
, which is uniformly bounded in time.
We assume that
is a bounded and measurable function. Let
be the eigenvalues of the operator
under homogeneous Neumann boundary condition on
, with
for
. Then first eigenvalue
is simple and real and corresponds to a positive eigenfunction
, which implies that
In this paper, we assume that
- (H1)
, .
Under the assumption (H1), Berestycki et al. [
4] obtained the existence and uniqueness of the cylinder front solution
of (
1) for
by applying spectral expansion and separation of variables, and showed that
must be in the form of
, where
satisfies
Under some additional assumptions on
, it was also proven in [
4] that the minimal speed
is the spreading speed of the solution with a compactly supported initial data. Recently, Li et al. [
3] obtained the locally exponential stability of the cylinder front solution in an exponentially weighted space. For the Cauchy problem (
1), it was shown in [
3] that the boundedness and the long time behavior of the solution are determined by that of
, and based on this conclusion, the author further investigated the global asymptotic stability of the cylinder waves and the asymptotic behavior of the solution in the
x direction as
for nonnegative initial data decaying exponentially or vanishing as
. Suppose that
, and denote
When
it was shown that
as
. Moreover, the global exponential stability of cylinder waves in exponentially weighted space was also obtained when
as
. When
is nonnegative and compactly supported in the cylinder, the global asymptotic stability of cylinder wave with critical speed was also studied in [
3].
Note that (
1) can be regarded as a simplified version of the nonlocal reaction-diffusion model studied in [
5] as follows
where
stands for the intensity of selection towards the optimal value
, and
implies that competitive ability depends not only on the spatial variable
x but also on the traits
of two competitive individuals. Note that (
2) is reduced by
,
and
in (
1). There are many works on the cylinder front solution and the spreading speed of (
2). We refer to [
6] for the existence of a cylinder front with
and
and [
7] for the existence of steady-state solutions and pulsating fronts with periodic
, as well as [
8] for the existence of cylinder waves and the spreading speed of (
2) in the moving environment with
. In addition, the spreading speed and the asymptotic behavior of the solution were studied in [
9] with a bounded
and a constant kernel
applying the Hamilton-Jacobi approach.
1.2. Main Assumptions and Results
In this paper, we consider the initial data decaying slower than any exponential function. Assume that there exists a function such that
- (H2)
for some constants .
Denote
which is equipped with the norm
. Throughout the paper, we assume that the initial function satisfies
We say
is a slowly decaying function, if there is a large constant
such that
Under (
3) and (
4),
decays more slowly than any exponentially decaying function as
, that is,
Two typical examples of (
3) and (
4) are given by
for large
x with
, or
for large
x with
. Note that when
satisfies (H2), (
3) and (
4), we have the following.
which indicates that the initial data considered in this paper are different from any of those studied in [
3].
Therefore, we study the accelerating propagation of (
1) with slowly decaying initial data, and the main theorem is stated as follows.
Theorem 1. Let g and K satisfy (H1), and suppose that satisfies (H2), (
3)
and (
4).
Then for any , , , and , there is such thatwhere , , and . Example 1. Under the same assumption in Theorem 1, we have that
(1)
if as , then (2)
if with as , then Next, we consider the spatial propagation of (
2) by applying the method in Theorem 1. The primary difficulty of this model stems from the complexity of the competition term
. For analytical convenience, we assume that
Description 1.
- (H3)
, and there exist and such that
Here
is the first eigenvalue of the operator
under homogeneous Neumann boundary condition on
, and we also denote the corresponding positive eigenfunction by
. Then it follows that
Our results for the acceleration propagation (
2) are stated as follows.
Corollary 1. Suppose that g and satisfy (H3), and let satisfy (H2), (
3)
and (
4).
Then the model (
2)
has the same propagation properties as in Theorem 1. Theorem 1 demonstrates that when the initial function exhibits slow decay characteristics (such as algebraic or sub-exponential decay), the solution of the nonlocal reaction-diffusion system (1) displays accelerating propagation. This means that for all subpopulations with distinct traits , their respective invasion fronts propagate at ever-increasing speeds as time tends to infinity. It is commonly said that the solution has infinite speeding speed when it satisfies the propagation property in Theorem 1. This result indicates that in nonlocal reaction-diffusion models, the propagation speed of a population depends not only on the diffusion coefficient and local growth rate but also, and more profoundly, on the decay rate of the initial distribution in the far-field spatial region. Slowly decaying initial conditions provide a sustained “spatial momentum” to the population, driving an acceleration process that surpasses the classic constant-speed traveling wave propagation mode.
From model (1) to the more general model (2), this conclusion remains valid under the assumption (H3) on the competition kernel. Model (2) incorporates selection intensity , an optimal trait , and a competition ability that depends on both space and traits, making it more general. Theorem 1 and Corollary 1 together illustrate that even with a more complex competition term, as long as the initial distribution decays slowly in the spatial direction and its trait structure can be separated from the spatial part via the eigenfunction , the essential feature of accelerating propagation—that level sets advance at an ever-increasing speed—persists. This reveals the profound dependence of propagation dynamics on the global geometric form of the initial condition (not merely its local support) in nonlocal models with spatial and trait structures.
From a mathematical perspective, “infinite spreading speed” means that the velocity of the propagation front grows without bound as time tends to infinity, rather than representing instantaneous transmission in the physical sense. In ecological contexts, this corresponds to species dispersing over very long distances in relatively short time scales—such as plant seeds being carried by wind, birds, or human activities that facilitate long-distance dispersal events. If we interpret the variable x differently—for example, by viewing it as the latitude on Earth—then the phenomenon of accelerating propagation in the model could be understood as the rapid expansion of a certain type of bird or insect, adapted to various latitudes, spreading from the equator (or a specific region) toward the North and South Poles.
Ecologically, this finding carries significant implications. It suggests that when a species (or a specific trait) exhibits a “long-tailed” distribution at the periphery of the introduced region—where density is very low but decays extremely slowly—its subsequent spatial expansion may far exceed predictions based on local diffusion or exponentially decaying initial conditions. For instance, in conservation biology and invasion ecology, assessing the potential expansion risk of a species solely by focusing on the density of its core distribution area or assuming rapid decay at its boundaries may severely underestimate its long-term dispersal capacity. This is particularly relevant for species capable of long-distance dispersal (e.g., via wind, water, or animal vectors), as their initial distributions are more likely to exhibit such slow decay characteristics, leading to unexpectedly rapid range expansion. Furthermore, in scenarios such as the intentional release of gene-drive organisms or genetically modified organisms, fine control over the spatial distribution of initially introduced individuals—especially avoiding the creation of low-density “pioneer” individuals at long distances—may be crucial for managing their propagation speed. This study provides a theoretical framework for quantitatively assessing propagation potential in such contexts.
1.3. Research Motivation for Slowly Decaying Initial Data and Its Induced Accelerating Propagation
The slowly decaying initial conditions—such as algebraic or sub-exponential decay—considered in this study are ecologically and biologically well-motivated. In many real-world scenarios of population dispersal and biological invasion, the initial spatial distribution of a species is often not compactly supported or exponentially bounded. Some examples are listed as follows.
Long-distance dispersal events: Seeds, insects, or microorganisms can be transported over long distances by wind, water currents, birds, or airplanes, resulting in sparse “pioneer individuals” far from the core population. Their density may be extremely low but decays slowly in space rather than abruptly vanishing.
Non-uniform introductions or historical remnants: In cases of intentional species release (e.g., biocontrol agents and genetically modified organisms) or residual populations after range contraction, the initial distribution may exhibit a “long-tail” pattern—very low density extending over a wide spatial domain.
Environmental heterogeneity and diverse dispersal strategies: In heterogeneous environments, populations may adopt multiple dispersal strategies, with some individuals moving to distant areas to explore new resources, thereby generating a slowly decaying spatial profile.
Therefore, studying propagation dynamics under slowly decaying initial data is crucial for accurately assessing the invasion risk of species that are capable of long-distance dispersal or that initially exhibit widespread but sparse distributions (e.g., invasive species, disease hosts, and genetically engineered organisms). The theoretical analysis presented here provides a mathematical foundation for understanding the phenomenon of accelerating propagation in such realistic contexts.
Slowly decaying initial data are not only pivotal in this study but also have extensive practical correspondence in numerous partial differential equations and ecological models, garnering sustained attention. In the classical reaction-diffusion equation
Hamel and Roques [
10] showed that the solution of (
5) has an infinite spreading speed under the Fisher-KPP assumption on
f, in the sense that, the level sets of the solutions move infinitely fast as time goes to infinity, and more accurate descriptions on the locations of level sets were also obtained. Subsequently, the accelerating propagation of (
5) with degenerated reaction function (namely
) was studied in [
11] and the exact separation between no acceleration and acceleration was provided. We refer to [
12] for the results about accelerating propagation in nonlocal dispersal equations. It is worth pointing out that the accelerating invasion was also studied in [
13] for the nonlocal reaction-diffusion model, where the optimal trait for survival depends linearly on the spatial variable, as follows
when the initial data satisfy the heavy-tailed condition in the direction
on the space-trait plane. Moreover, the accelerating propagation of the following reaction-diffusion equation in cylinder
was studied in [
14], when
is a slowly decaying function for some
.
The remainder of this paper is organized as follows.
Section 2 proves the main results (Theorem 1) on accelerating propagation for model (1).
Section 3 extends the key conclusions to the more general model (2) and prove the corresponding corollary (Corollary 1). Finally,
Section 4 provides a summary and discussion of the mathematical implications and ecological insights derived from the obtained results.