Overlap properties of geometric expanders

The {\em overlap number} of a finite $(d+1)$-uniform hypergraph $H$ is defined as the largest constant $c(H)\in (0,1]$ such that no matter how we map the vertices of $H$ into $\R^d$, there is a point covered by at least a $c(H)$-fraction of the simplices induced by the images of its hyperedges. In~\cite{Gro2}, motivated by the search for an analogue of the notion of graph expansion for higher dimensional simplicial complexes, it was asked whether or not there exists a sequence $\{H_n\}_{n=1}^\infty$ of arbitrarily large $(d+1)$-uniform hypergraphs with bounded degree, for which $\inf_{n\ge 1} c(H_n)>0$. Using both random methods and explicit constructions, we answer this question positively by constructing infinite families of $(d+1)$-uniform hypergraphs with bounded degree such that their overlap numbers are bounded from below by a positive constant $c=c(d)$. We also show that, for every $d$, the best value of the constant $c=c(d)$ that can be achieved by such a construction is asymptotically equal to the limit of the overlap numbers of the complete $(d+1)$-uniform hypergraphs with $n$ vertices, as $n\rightarrow\infty$. For the proof of the latter statement, we establish the following geometric partitioning result of independent interest. For any $d$ and any $\epsilon>0$, there exists $K=K(\epsilon,d)\ge d+1$ satisfying the following condition. For any $k\ge K$, for any point $q \in \mathbb{R}^d$ and for any finite Borel measure $\mu$ on $\mathbb{R}^d$ with respect to which every hyperplane has measure $0$, there is a partition $\mathbb{R}^d=A_1 \cup \ldots \cup A_{k}$ into $k$ measurable parts of equal measure such that all but at most an $\epsilon$-fraction of the $(d+1)$-tuples $A_{i_1},\ldots,A_{i_{d+1}}$ have the property that either all simplices with one vertex in each $A_{i_j}$ contain $q$ or none of these simplices contain $q$

Uniformizing the Stacks of Abelian Sheaves

Elliptic sheaves (which are related to Drinfeld modules) were introduced by Drinfeld and further studied by Laumon--Rapoport--Stuhler and others. They can be viewed as function field analogues of elliptic curves and hence are objects "of dimension 1". Their higher dimensional generalisations are called abelian sheaves. In the analogy between function fields and number fields, abelian sheaves are counterparts of abelian varieties. In this article we study the moduli spaces of abelian sheaves and prove that they are algebraic stacks. We further transfer results of Cerednik--Drinfeld and Rapoport--Zink on the uniformization of Shimura varieties to the setting of abelian sheaves. Actually the analogy of the Cerednik--Drinfeld uniformization is nothing but the uniformization of the moduli schemes of Drinfeld modules by the Drinfeld upper half space. Our results generalise this uniformization. The proof closely follows the ideas of Rapoport--Zink. In particular, analogies of $p$-divisible groups play an important role. As a crucial intermediate step we prove that in a family of abelian sheaves with good reduction at infinity, the set of points where the abelian sheaf is uniformizable in the sense of Anderson, is formally closed.Comment: Final version, appears in "Number Fields and Function Fields - Two Parallel Worlds", Papers from the 4th Conference held on Texel Island, April 2004, edited by G. van der Geer, B. Moonen, R. Schoo

Quantum Symmetries and Strong Haagerup Inequalities

In this paper, we consider families of operators $\{x_r\}_{r \in \Lambda}$ in a tracial C$^\ast$-probability space $(\mathcal A, \phi)$, whose joint $\ast$-distribution is invariant under free complexification and the action of the hyperoctahedral quantum groups $\{H_n^+\}_{n \in \N}$. We prove a strong form of Haagerup's inequality for the non-self-adjoint operator algebra $\mathcal B$ generated by $\{x_r\}_{r \in \Lambda}$, which generalizes the strong Haagerup inequalities for $\ast$-free R-diagonal families obtained by Kemp-Speicher \cite{KeSp}. As an application of our result, we show that $\mathcal B$ always has the metric approximation property (MAP). We also apply our techniques to study the reduced C$^\ast$-algebra of the free unitary quantum group $U_n^+$. We show that the non-self-adjoint subalgebra $\mathcal B_n$ generated by the matrix elements of the fundamental corepresentation of $U_n^+$ has the MAP. Additionally, we prove a strong Haagerup inequality for $\mathcal B_n$, which improves on the estimates given by Vergnioux's property RD \cite{Ve}

Nonlinear spectral calculus and super-expanders

Nonlinear spectral gaps with respect to uniformly convex normed spaces are shown to satisfy a spectral calculus inequality that establishes their decay along Cesaro averages. Nonlinear spectral gaps of graphs are also shown to behave sub-multiplicatively under zigzag products. These results yield a combinatorial construction of super-expanders, i.e., a sequence of 3-regular graphs that does not admit a coarse embedding into any uniformly convex normed space.Comment: Typos fixed based on referee comments. Some of the results of this paper were announced in arXiv:0910.2041. The corresponding parts of arXiv:0910.2041 are subsumed by the current pape

Multihost experimental evolution of a plant RNA virus reveals local adaptation and host specific mutations

[EN] For multihost pathogens, adaptation to multiple hosts has important implications for both applied and basic research. At the applied level, it is one of the main factors determining the probability and the severity of emerging disease outbreaks. At the basic level, it is thought to be a key mechanism for the maintenance of genetic diversity both in host and pathogen species. Using Tobacco etch potyvirus (TEV) and four natural hosts, we have designed an evolution experiment whose strength and novelty are the use of complex multicellular host organism as hosts and a high level of replication of different evolutionary histories and lineages. A pattern of local adaptation, characterized by a higher infectivity and virulence on host(s) encountered during the experimental evolution was found. Local adaptation only had a cost in terms of performance on other hosts in some cases. We could not verify the existence of a cost for generalists, as expected to arise from antagonistic pleiotropy and other genetic mechanisms generating a fitness trade-off between hosts. This observation confirms that this classical theoretical prediction lacks empirical support. We discuss the reasons for this discrepancy between theory and experiment in the light of our results. The analysis of full genome consensus sequences of the evolved lineages established that all mutations shared between lineages were host specific. A low degree of parallel evolution was observed, possibly reflecting the various adaptive pathways available for TEV in each host. Altogether, these results reveal a strong adaptive potential of TEV to new hosts without severe evolutionary constraints.We thank Francisca de la Iglesia and Angels Prosper for excellent technical assistance and Mark Zwart and two anonymous reviewers for their helpful comments on a previous version of the manuscript. This research was supported by the Spanish Ministry of Science and Innovation grant BFU2009-06993 to S. F. E. S. B. was supported by the JAE-doc program from Consejo Superior de Investigaciones Cientificas and G. L. was supported by the Human Frontier Science Program, grant RGP0012/2008.Bedhomme, S.; Lafforgue, G.; Elena Fito, SF. (2012). Multihost experimental evolution of a plant RNA virus reveals local adaptation and host specific mutations. Molecular Biology and Evolution. 29(5):1481-1492. https://doi.org/10.1093/molbev/msr314S1481149229

Red Queen Coevolution on Fitness Landscapes

Species do not merely evolve, they also coevolve with other organisms. Coevolution is a major force driving interacting species to continuously evolve ex- ploring their fitness landscapes. Coevolution involves the coupling of species fit- ness landscapes, linking species genetic changes with their inter-specific ecological interactions. Here we first introduce the Red Queen hypothesis of evolution com- menting on some theoretical aspects and empirical evidences. As an introduction to the fitness landscape concept, we review key issues on evolution on simple and rugged fitness landscapes. Then we present key modeling examples of coevolution on different fitness landscapes at different scales, from RNA viruses to complex ecosystems and macroevolution.Comment: 40 pages, 12 figures. To appear in "Recent Advances in the Theory and Application of Fitness Landscapes" (H. Richter and A. Engelbrecht, eds.). Springer Series in Emergence, Complexity, and Computation, 201