Let $\mathcal {O}(\pi )$ denote the number of odd parts in an integer partition $\pi$. In 2005, Stanley introduced a new statistic $\operatorname {srank}(\pi )=\mathcal {O}(\pi )-\mathcal {O}(\pi ')$, where $\pi '$ is the conjugate of $\pi$. Let $p(r,\,m;n)$ denote the number of partitions of $n$ with srank congruent to $r$ modulo $m$. Generating function identities, congruences and inequalities for $p(0,\,4;n)$ and $p(2,\,4;n)$ were then established by a number of mathematicians, including Stanley, Andrews, Swisher, Berkovich and Garvan. Motivated by these works, we deduce some generating functions and inequalities for $p(r,\,m;n)$ with $m=16$ and $24$. These results are refinements of some inequalities due to Swisher.

Given groups $A$ and $B$, what is the minimal commutator length of the 2020th (for instance) power of an element $g\in A*B$ not conjugate to elements of the free factors? The exhaustive answer to this question is still unknown, but we can give an almost answer: this minimum is one of two numbers (simply depending on $A$ and $B$). Other similar problems are also considered.

Experimental results on the immune response to cancer indicate that activation of cytotoxic T lymphocytes (CTLs) through interactions with dendritic cells (DCs) can trigger a change in CTL migration patterns. In particular, while CTLs in the pre-activation state move in a non-local search pattern, the search pattern of activated CTLs is more localised. In this paper, we develop a kinetic model for such a switch in CTL migration modes. The model is formulated as a coupled system of balance equations for the one-particle distribution functions of CTLs in the pre-activation state, activated CTLs and DCs. CTL activation is modelled via binary interactions between CTLs in the pre-activation state and DCs. Moreover, cell motion is represented as a velocity-jump process, with the running time of CTLs in the pre-activation state following a long-tailed distribution, which is consistent with a Lévy walk, and the running time of activated CTLs following a Poisson distribution, which corresponds to Brownian motion. We formally show that the macroscopic limit of the model comprises a coupled system of balance equations for the cell densities, whereby activated CTL movement is described via a classical diffusion term, whilst a fractional diffusion term describes the movement of CTLs in the pre-activation state. The modelling approach presented here and its possible generalisations are expected to find applications in the study of the immune response to cancer and in other biological contexts in which switch from non-local to localised migration patterns occurs.

In this paper, we prove existence results of a one-dimensional periodic solution to equations with the fractional Laplacian of order $s\in (1/2,1)$, singular nonlinearity and gradient term under various situations, including nonlocal contra-part of classical Lienard vector equations, as well other nonlocal versions of classical results know only in the context of second-order ODE. Our proofs are based on degree theory and Perron's method, so before that we need to establish a variety of priori estimates under different assumptions on the nonlinearities appearing in the equations. Besides, we obtain also multiplicity results in a regime where a priori bounds are lost and bifurcation from infinity occurs.

It is proved that if $\varphi \colon A\to B$ is a local homomorphism of commutative noetherian local rings, a nonzero finitely generated B-module N whose flat dimension over A is at most $\operatorname {edim} A - \operatorname {edim} B$ is free over B and $\varphi $ is a special type of complete intersection. This result is motivated by a ‘patching method’ developed by Taylor and Wiles and a conjecture of de Smit, proved by the first author, dealing with the special case when N is flat over A.

In this paper, we establish an infinite series expansion of Leray–Trudinger inequality, which is closely related with Hardy inequality and Moser Trudinger inequality. Our result extends early results obtained by Mallick and Tintarev [A. Mallick and C. Tintarev. An improved Leray-Trudinger inequality. Commun. Contemp. Math. 20 (2018), 17501034. OP 21] to the case with many logs. It should be pointed out that our result is about series expansion of Hardy inequality under the case $p=n$, which case is not considered by Gkikas and Psaradakis in [K. T. Gkikas and G. Psaradakis. Optimal non-homogeneous improvements for the series expansion of Hardy's inequality. Commun. Contemp. Math. doi:10.1142/S0219199721500310]. However, we can't obtain the optimal form by our method.

In this paper we are interested in comparing the spectra of two elliptic operators acting on a closed minimal submanifold of the Euclidean unit sphere. Using an approach introduced by Savo in [A Savo. Index Bounds for Minimal Hypersurfaces of the Sphere. Indiana Univ. Math. J. 59 (2010), 823-837.], we are able to compare the eigenvalues of the stability operator acting on sections of the normal bundle and the Hodge Laplacian operator acting on $1$-forms. As a byproduct of the technique and under a suitable hypothesis on the Ricci curvature of the submanifold we obtain that its first Betti's number is bounded from above by a multiple of the Morse index, which provide evidence for a well-known conjecture of Schoen and Marques & Neves in the setting of higher codimension.

We construct new optimal $L^{p}$ Hardy-type inequalities for elliptic Schrödinger-type operators with a potential term.

We consider inverse nodal problems for the Sturm–Liouville operators on the tree graphs. Can only dense nodes distinguish the tree graphs? In this paper it is shown that the data of dense-nodes uniquely determines the potential (up to a constant) on the tree graphs. This provides interesting results for an open question implied in the paper.