Scalar inferences (SIs) are upper-bounding inferences associated with the use of semantically lower-bounded scalar expressions. One of the current debates regarding these inferences concerns their inferential pattern, specifically whether SIs are uniform or diverse across scales. This study follows the work on scalar diversity yet introduces two changes: First, we reexamine, from a different perspective, two structural properties of scales identified as accounting for SI diversity (boundedness and distance). Second, we analyze our data using both traditional regression analysis and complementary cluster analysis. The regression analysis demonstrates that our reexamination of the structural properties provides a more effective model, which also emphasizes the relationship between boundedness and distance. Specifically, we propose that boundedness fixes distance. The cluster analysis demonstrates two scale types: given-scales, which have an entrenched scalar construal, trigger SIs robustly; and volatile-scales, which have a fluctuant scalar construal, trigger SIs inconsistently. Building on these two scale types, we propose a necessary distinction between the conceptualization of a scale, which is diverse across different scales, and the actual derivation of the SI, which is uniform for all scales, once a scale has been construed. This distinction, we propose, explains how diversity can coexist alongside uniformity.

Using the technique of Gabor analysis, we characterize the boundedness of $e^{i\Delta }: W^{p_1,q_1}_m\rightarrow W^{p_2,q_2}$ with modulation and translation operators, where and m is a v-moderate weight. The sharp exponents for the boundedness are also characterized in the case of power weight.

This paper deals with the following quasilinear chemotaxis system with consumption of chemoattractant

\[ \left\{\begin{array}{@{}ll} u_t=\Delta u^{m}-\nabla\cdot(u\nabla v),\quad & x\in \Omega,\quad t>0,\\ v_t=\Delta v-uv,\quad & x\in \Omega,\quad t>0\\ \end{array}\right. \]

$\Omega \subset \mathbb {R}^N(N=3,\,4,\,5)$

$\partial \Omega$

$m>\max \{1,\,\frac {3N-2}{2N+2}\}$

$(\bar {u}_0,\,0)$

$t\rightarrow \infty$

$\bar {u}_0=\frac {1}{|\Omega |}\int _\Omega u_0$

$m>\frac {3N-2}{2N}$

$N\geq 3$

$m>\frac {3N}{2N+2}$

$N\geq 2$

For a real number $0<\epsilon <1/3$, we show that the anti-canonical volume of an $\epsilon $-klt Fano $3$-fold is at most $3,200/\epsilon ^4$, and the order $O(1/\epsilon ^4)$ is sharp.

In this note, we start on the study of the sufficient conditions for the boundedness of Hausdorff operators

$$ \begin{align*}(\mathcal{H}_{K,\mu}f)(z):=\int_{\mathbb{D}}K(w)f(\sigma_w(z))d\mu(w)\end{align*} $$

$\mu $

$\mu $

$\mathbb {D}$

$\sigma _w(z)$

$\mathbb {D}$

Conventional preytaxis systems assume that prey-tactic velocity is proportional to the prey density gradient. However, many experiments exploring the predator–prey interactions show that it is the predator’s acceleration instead of velocity that is proportional to the prey density gradient in the prey-tactic movement, which we call preytaxis with prey-induced acceleration. Mathematical models of preytaxis with prey-induced acceleration were proposed by Arditi et al. ((2001) Theor. Popul. Biol. 59(3), 207–221) and Sapoukhina et al. ((2003) Am. Nat. 162(1), 61–76) to interpret the spatial heterogeneity of predators and prey observed in experiments. This paper is devoted to exploring the qualitative behaviour of such preytaxis systems with prey-induced acceleration and establishing the global existence of classical solutions with uniform-in-time bounds in all spatial dimensions. Moreover, we prove the global stability of spatially homogeneous prey-only and coexistence steady states with decay rates under certain conditions on system parameters. For the parameters outside the stability regime, we perform linear stability analysis to find the possible patterning regimes and use numerical simulations to demonstrate that spatially inhomogeneous time-periodic patterns will typically arise from the preytaxis system with prey-induced acceleration. Noticing that conventional preytaxis systems are unable to produce spatial patterns, our results imply that the preytaxis with prey-induced acceleration is indeed more appropriate than conventional preytaxis to interpret the spatial heterogeneity resulting from predator–prey interactions.

We study the boundedness and compactness of weighted composition operators acting on weighted Bergman spaces and weighted Dirichlet spaces by using the corresponding Carleson measures. We give an estimate for the norm and the essential norm of weighted composition operators between weighted Bergman spaces as well as the composition operators between weighted Hilbert spaces.

This study considers a model for oncolytic virotherapy, as given by the reaction–diffusion–taxis system

\[\begin{eqnarray*} \left\{ \begin{array}{l} u_t = \Delta u - \nabla (u\nabla v)-\rho uz, \\ v_t = - (u+w)v, \\ w_t = D_w \Delta w - w + uz, \\ z_t = D_z \Delta z - z - uz + \beta w, \end{array} \right. \end{eqnarray*}\]

Previous analysis has asserted that for all reasonably regular initial data, an associated no-flux type initial-boundary value problem admits a global classical solution, and that this solution is bounded if β < 1, whereas whenever β > 1 and $({1}/{|\Omega |})\int _\Omega u(\cdot ,0) > 1/(\beta -1)$, infinite-time blow-up occurs at least in the particular case when ρ = 0.

In order to provide an appropriate complement to this, the current study reveals that for any ρ ⩾ 0 and arbitrary β > 0, at each prescribed level γ ∈ (0, 1/(β − 1)+) one can identify an L∞-neighbourhood of the homogeneous distribution (u, v, w, z) ≡ (γ, 0, 0, 0) within which all initial data lead to globally bounded solutions that stabilize towards the constant equilibrium (u∞, 0, 0, 0) with some u∞ > 0.

In this paper, we investigate the global boundedness, asymptotic stability and pattern formation of predator–prey systems with density-dependent prey-taxis in a two-dimensional bounded domain with Neumann boundary conditions, where the coefficients of motility (diffusiq‘dfdon) and mobility (prey-taxis) of the predator are correlated through a prey density-dependent motility function. We establish the existence of classical solutions with uniform-in time bound and the global stability of the spatially homogeneous prey-only steady states and coexistence steady states under certain conditions on parameters by constructing Lyapunov functionals. With numerical simulations, we further demonstrate that spatially homogeneous time-periodic patterns, stationary spatially inhomogeneous patterns and chaotic spatio-temporal patterns are all possible for the parameters outside the stability regime. We also find from numerical simulations that the temporal dynamics between linearised system and nonlinear systems are quite different, and the prey density-dependent motility function can trigger the pattern formation.

This paper deals with the global existence for a class of Keller–Segel model with signal-dependent motility and general logistic term under homogeneous Neumann boundary conditions in a higher-dimensional smoothly bounded domain, which can be written as

$$\eqalign{& u_t = \Delta (\gamma (v)u) + \rho u-\mu u^l,\quad x\in \Omega ,\;t > 0, \cr & v_t = \Delta v-v + u,\quad x\in \Omega ,\;t > 0.} $$

$$l > \max \left\{ {\displaystyle{{n + 2} \over 2},2} \right\},$$

$$\left( {{\left( {\displaystyle{{\rho _ + } \over \mu }} \right)}^{1/(l-1)},{\left( {\displaystyle{{\rho _ + } \over \mu }} \right)}^{1/(l-1)}} \right)$$

We study the boundedness of Toeplitz operators with locally integrable symbols on Bergman spaces Ap(Ω), 1 < p < ∞, where Ω ⊂ ℂ is a bounded simply connected domain with polygonal boundary. We give sufficient conditions for the boundedness of generalized Toeplitz operators in terms of ‘averages’ of symbol over certain Cartesian squares. We use the Whitney decomposition of Ω in the proof. We also give examples of bounded Toeplitz operators on Ap(Ω) in the case where polygon Ω has such a large corner that the Bergman projection is unbounded.

This paper investigates the global well-posedness of a class of reaction–advection–diffusion models with nonlinear diffusion and Lotka–Volterra dynamics. We prove the existence and uniform boundedness of the global-in-time solutions to the fully parabolic systems under certain growth conditions on the diffusion and sensitivity functions. Global existence and uniform boundedness of the corresponding parabolic–elliptic system are also obtained. Our results suggest that attraction (positive taxis) inhibits blowups in Lotka–Volterra competition systems.

We derive a stage-structured model for an insect population in which a larva matures on reaching a certain size, and in which there is intra-specific competition among larvae that hinders their development, thereby prolonging the larval phase. The model, a system of delay differential equations for the total numbers of adults and larvae, assumes two forms. One of these is a system with a variable state-dependent time delay determined by a threshold condition, the other has constant and distributed delays, a size-like independent variable replacing time t, and no threshold condition. We prove theorems on boundedness and on the linear stability of equilibria.

The purpose of this paper is to characterize positive measure $\mu$ on the unit disk such that the analytic Morrey space $\mathcal{A}{{\mathcal{L}}_{p,\eta }}$ is boundedly and compactly embedded to the tent space

$$\mathcal{J}_{q,1-\frac{q}{p}\left( 1-\eta \right)}^{\infty }\left( \mu \right)$$

for the case $1\,\le \,q\,\le \,p\,<\,\infty$ respectively. As an application, these results are used to establish the boundedness and compactness of integral operators and multipliers between analytic Morrey spaces.