Scientific

For a number field $K$, the P\'olya group of $K$, denoted by $Po(K)$, is the subgroup of the ideal class group of $K$ generated by the classes of the products of maximal ideals of $K$ with the same norm. In this talk, after reviewing some results concerning $Po(K)$, I will generalize this notion to the relative P\'olya group $Po(K/F)$, for $K/F$ a finite extension of number fields. Accordingly, I will generalize some results in the literature about P\'olya groups to the relative case. Then, due to some essential observations, I will explain why we need to modify the notion of the relative P\'olya group to the Ostrowski quotient $Ost(K/F)$ to get a more 'accurate' generalization of $Po(K)$. The talk is based on a joint work with Ali Rajaei (Tarbiat Modares University) and Ehsan Shahoseini (Institute For Research In Fundamental Sciences).

In 1973, assuming the Riemann hypothesis (RH), Montgomery studied the vertical distribution of zeta zeros, and conjectured that they behave like the eigenvalues of some random matrices. We will discuss some models for zeta zeros starting from the random matrix model but going beyond it and related questions, conjectures and results on statistical information on the zeros. In particular, assuming RH and a conjecture of Chan for how often gaps between zeros can be close to a fixed non-zero value, we will discuss our proof of a conjecture of Berry (1988) for the number variance of zeta zeros, in a regime where random matrix models alone do not accurately predict the actual behavior (based on joint work with Meghann Moriah Lugar and Micah B. Milinovich).

Skeletal muscle is composed of cells collectively referred to as fibers, which themselves contain contractile proteins arranged longtitudinally into sarcomeres. These latter respond to signals from the nervous system, and contract; unlike cardiac muscle, skeletal muscles can respond to voluntary control. Muscles react to mechanical forces - they contain connective tissue and fluid, and are linked via tendons to the skeletal system - but they also are capable of activation via stimulation (and hence, contraction) of the sacromeres. The restorative along-fibre force introduce strong mechanical anisotropy, and depend on departures from a characteristic length of the sarcomeres; diseases such as cerebral palsy cause this characteristic length to change, thereby impacting muscle force. In the 1910s, A.V. Hill [1] posited a mathematical description of skeletal muscles which approximated muscle as a 1-dimensional nonlinear and massless spring. This has been a remarkably successful model, and remains in wide use. Yet skeletal muscle is three dimensional, has mass, and a fairly complicated structure. Are these features important? What insights are gained if we include some of this complexity in our models? Many mathematical questions of interest in skeletal muscle mechanics arise: how to model this system, how to discretize it, and what theoretical properties does it have? In this talk, we survey recent work on the modeling, parameter estimation, simulation and validation of a fully 3-D continuum elasticity approach for skeletal muscle dynamics. This is joint work based on a long-standing collaboration with James Wakeling (Dept. of Biomedical Physiology and Kinesiology, SFU).

The evolution and maintenance of cooperation is a fundamental problem in evolutionary biology. Because cooperative behaviors impose a cost, Cooperators are vulnerable to exploitation by Defectors that do not pay the cost to cooperate but still benefit from the cooperation of others. The bacteriophage $\Phi_6$ exhibits cooperative and defective phenotypes in infection: during replication, phages produce essential proteins in the host cell cytoplasm. Coinfection between multiple phages is possible. A given phage cannot guarantee exclusive access to its own proteins, so Cooperators contribute to the common pool of proteins while Defectors contribute less and instead appropriate proteins from Cooperators. Previous experimental work found that $\Phi_6$ was trapped in a prisoner's dilemma, predicting that the cooperative phenotype should disappear. Here we propose that environmental feedback, or interplay between phage and host densities, can maintain cooperation in $\Phi_6$ populations by modulating the rate of co-infection and shifting the advantages of cooperation vs. defection. We build and analyze an ODE model and find that for a wide range of parameter values, environmental feedback allows Cooperation to survive.

Subconvexity problems have maintained extreme interest in analytic number theory for decades. Critical barriers such as the convexity, Burgess, and Weyl bounds hold particular interest because one usually needs to drastically adjust the analytic techniques involved in order to break through them. It has recently come to light that shifted Dirichlet series can be used to obtain subconvexity results. While these Dirichlet series do not admit Euler products, they are amenable to study via spectral methods. In this talk, we construct a shifted multiple Dirichlet series (MDS) and leverage its analytic continuation via spectral decompositions to obtain the Weyl bound in the conductor-aspect for the L-function of a holomorphic cusp form twisted by an arbitrary Dirichlet character. This improves upon the corresponding bound for quadratic characters obtained by Iwaniec-Conrey in 2000. This work is joint with Jeff Hoffstein, Nikos Diamantis, and Min Lee.