We construct a hereditarily indecomposable Banach space with dual space isomorphic to$ℓ$_{1}. Every bounded linear operator on this space is expressible as λ$I$+$K$, with λ a scalar and$K$compact.

We provide a refinement of the Poincaré inequality on the torus $\mathbb{T}^{d}$ : there exists a set $\mathcal{B} \subset \mathbb{T} ^{d}$ of directions such that for every $\alpha \in \mathcal{B}$ there is a $c_{\alpha } > 0$ with $$\begin{aligned} \|\nabla f\|_{L^{2}(\mathbb{T}^{d})}^{d-1} \| \langle \nabla f, \alpha \rangle \|_{L^{2}(\mathbb{T}^{d})} \geq c_{\alpha }\|f\| _{L^{2}(\mathbb{T}^{d})}^{d} \quad \mbox{for all}~f\in H^{1}\bigl( \mathbb{T}^{d}\bigr)~ \mbox{with mean 0.} \end{aligned}$$ The derivative $\langle \nabla f, \alpha \rangle $ does not detect any oscillation in directions orthogonal to $\alpha $ , however, for certain $\alpha $ the geodesic flow in direction $\alpha $ is sufficiently mixing to compensate for that defect. On the two-dimensional torus $\mathbb{T}^{2}$ the inequality holds for $\alpha = (1, \sqrt{2})$ but is not true for $\alpha = (1,e)$ . Similar results should hold at a great level of generality on very general domains.

Over time, a population acquires neutral genetic substitutions as a consequence of random drift. A famous result in population genetics asserts that the rate, K, at which these substitutions accumulate in the population coincides with the mutation rate, u, at which they arise in individuals: K = u. This identity enables genetic sequence data to be used as a “molecular clock” to estimate the timing of evolutionary events. While the molecular clock is known to be perturbed by selection, it is thought that K = u holds very generally for neutral evolution. Here we show that asymmetric spatial population structure can alter the molecular clock rate for neutral mutations, leading to either K<u or K>u. Our results apply to a general class of haploid, asexually reproducing, spatially structured populations. Deviations from K = u occur because mutations arise unequally at different sites and have different probabilities of fixation depending on where they arise. If birth rates are uniform across sites, then K
u. In general, K can take any value between 0 and Nu. Our model can be applied to a variety of population structures. In one example, we investigate the accumulation of genetic mutations in the small intestine. In another application, we analyze over 900 Twitter networks to study the effect of network topology on the fixation of neutral innovations in social evolution.

No abstract uploaded!

No abstract uploaded!