Let$E$ç$S$^{1}be a set with Minkowski dimension$d(E)1$. We consider the Hardy-Littlewood maximal function, the Hilbert transform and the maximal Hilbert transform along the directions of$E$. The main result of this paper shows that these operators are bounded on$L$_{$rad$}^{$p$}(R^{2}) for$p>1+d(E)$and unbounded when$p<1+d(E)$. We also give some end-point results.

This paper studies the dynamics of a network-based SIS epidemic model with nonmonotone incidence rate. This type of nonlinear incidence can be used to describe the psychological effect of certain diseases spread in a contact network at high infective levels. We first find a threshold value for the transmission rate. This value completely determines the dynamics of the model and interestingly, the threshold is not dependent on the functional form of the nonlinear incidence rate. Furthermore, if the transmission rate is less than or equal to the threshold value, the disease will die out. Otherwise, it will be permanent. Numerical experiments are given to illustrate the theoretical results. We also consider the effect of the nonlinear incidence on the epidemic dynamics.

In this article, we continue the work in Guan-Li and study a normalized hypersurface flow in the more general ambient setting of warped product spaces. This flow preserves the volume of the bounded domain enclosed by a graphical hypersurface, and monotonically decreases the hypersurface area. As an application, the isoperimetric problem in warped product spaces is solved for such domains.

Comparing DNA and protein sequence groups plays an important role in biological evolutionary relationship research. Despite many methods available for sequence comparison, only a few can be used for group comparison. In this study, we propose a novel approach using convex hulls. We use statistical information contained within the sequences to represent each sequence as a point in high dimensional space. We find that the points belonging to one biological group are located in a different region of space than points belonging to other biological groups. To be more precise, the convex hull of the points from one group are disjoint from the convex hulls of points from other groups. This finding allows us to do phylogenetic analysis for groups in an efficient way. Five different theorems are presented for checking whether two convex hulls intersect or are disjoint. Test results for datasets related to HRV, HPV, Ebolavirus, PKC and protein phosphatase domains demonstrate that our method performs well and provides a new tool for studying group phylogeny. More significantly, the convex analysis presents a new way to search for sequences belonging to a biological group by examining points within the group’s convex hull.

We undertake a systematic study of the infinitesimal geometry of the Thurston metric, showing that the topology, convex geometry and metric geometry of the tangent and cotangent spheres based at any marked hyperbolic surface representing a point in Teichmüller space can recover the marking and geometry of this marked surface. We then translate the results concerning the infinitesimal structures to global geometric statements for the Thurston metric, most notably deriving rigidity statements for the Thurston metric analogous to the celebrated Royden theorem.