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Suppose that we have $$n$$ agents and $$n$$ items which lie in a shared metric space. We would like to match the agents to items such that the total distance from agents to their matched items is as small as possible. However, instead of having direct access to distances in the metric, we only have each agent's ranking of the items in order of distance. Given this limited information, what is the minimum possible worst-case approximation ratio (known as the \emph{distortion}) that a matching mechanism can guarantee? Previous work by \citet{CFRF+16} proved that the (deterministic) Serial Dictatorship mechanism has distortion at most $$2^n - 1$. We improve this by providing a simple deterministic mechanism that has distortion $O(n^2)$. We also provide the first nontrivial lower bound on this problem, showing that any matching mechanism (deterministic or randomized) must have worst-case distortion $$\Omega(\log n)$$. In addition to these new bounds, we show that a large class of truthful mechanisms derived from Deferred Acceptance all have worst-case distortion at least $2^n - 1$, and we find an intriguing connection between \emph{thin matchings} (analogous to the well-known thin trees conjecture) and the distortion gap between deterministic and randomized mechanisms. 

Colonies of the arboreal turtle ant create networks of trails that link nests and food sources on the graph formed by branches and vines in the canopy of the tropical forest. Ants put down a volatile pheromone on the edges as they traverse them. At each vertex, the next edge to traverse is chosen using a decision rule based on the current pheromone level. There is a bidirectional flow of ants around the network. In a previous field study, it was observed that the trail networks approximately minimize the number of vertices, thus solving a variant of the popular shortest path problem without any central control and with minimal computational resources. We propose a biologically plausible model, based on a variant of the reinforced random walk on a graph, which explains this observation and suggests surprising algorithms for the shortest path problem and its variants. Through simulations and analysis, we show that when the rate of flow of ants does not change, the dynamics converges to the path with the minimum number of vertices, as observed in the field. The dynamics converges to the shortest path when the rate of flow increases with time, so the colony can solve the shortest path problem merely by increasing the flow rate. We also show that to guarantee convergence to the shortest path, bidirectional flow and a decision rule dividing the flow in proportion to the pheromone level are necessary, but convergence to approximately short paths is possible with other decision rules. 

Given n points in 𝓁_p^d, we consider the problem of partitioning points into k clusters with associated centers. The cost of a clustering is the sum of p-th powers of distances of points to their cluster centers. For p ∈ [1,2], we design sketches of size poly(log(nd),k,1/ε) such that the cost of the optimal clustering can be estimated to within factor 1+ε, despite the fact that the compressed representation does not contain enough information to recover the cluster centers or the partition into clusters. This leads to a streaming algorithm for estimating the clustering cost with space poly(log(nd),k,1/ε). We also obtain a distributed memory algorithm, where the n points are arbitrarily partitioned amongst m machines, each of which sends information to a central party who then computes an approximation of the clustering cost. Prior to this work, no such streaming or distributed-memory algorithm was known with sublinear dependence on d for p ∈ [1,2).