We derive the alternating arm exponents of the critical Ising model. We obtain six different patterns of alternating boundary arm exponents which correspond to the boundary conditions (⊖⊕), (⊖ free) and (free free), and the alternating interior arm exponents.

Wehrl used Glauber coherent states to define a map from quantum density matrices to classical phase space densities and conjectured that for Glauber coherent states the mininimum classical entropy would occur for density matrices equal to projectors onto coherent states. This was proved by Lieb in 1978 who also extended the conjecture to Bloch SU(2) spin-coherent states for every angular momentum$J$. This conjecture is proved here. We also recall our 1991 extension of the Wehrl map to a quantum channel from J to $${K=J+\frac{1}{2}, J+1, ... ,}$$ with $${K=\infty}$$ corresponding to the Wehrl map to classical densities. These channels were later recognized as the optimal quantum cloning channels. For each$J$and $${J < K \leqslant \infty}$$ we show that the minimal output entropy for the channels occurs for a J coherent state. We also show that coherent states both Glauber and Bloch minimize any concave functional, not just entropy.

We show that direct limit completions of vertex tensor categories inherit vertex and braided tensor category structures, under conditions that hold for example for all known Virasoro and affine Lie algebra tensor categories. A consequence is that the theory of vertex operator (super)algebra extensions also applies to infinite-order extensions. As an application, we relate rigid and non-degenerate vertex tensor categories of certain modules for both the affine vertex superalgebra of osp(1|2) and the N=1 super Virasoro algebra to categories of Virasoro algebra modules via certain cosets.

The stochasticity of gene expression is manifested in the fluctuations of mRNA and protein copy numbers within a cell lineage over time. While data of this type can be obtained for many generations, most mathematical models are unsuitable to interpret such data since they assume non-growing cells. Here we develop a theoretical approach that quantitatively links the frequency content of lineage data to subcellular dynamics. We elucidate how the position, height, and width of the peaks in the power spectrum provide a distinctive fingerprint that encodes a wealth of information about mechanisms controlling transcription, translation, replication, degradation, bursting, promoter switching, cell cycle duration, cell division, gene dosage compensation, and cell size homeostasis. Predictions are confirmed by analysis of single-cell Escherichia coli data obtained using fluorescence microscopy. Furthermore, by matching the experimental and theoretical power spectra, we infer the temperature-dependent gene expression parameters, without the need of measurements relating fluorescence intensities to molecule numbers.

A celebrated theorem of Kapranov states that the Atiyah class of the tangent bundle of a complex manifold X makes TX[−1] into a Lie algebra object in D+(X), the bounded below derived category of coherent sheaves on X. Furthermore, Kapranov proved that, for a Kähler manifold X, the Dolbeault resolution \Omega(T{1,0} X ) of TX[−1]is an L∞ algebra. In this paper, we prove that Kapranov’s theorem holds in much wider generality for vector bundles over Lie pairs. Given a Lie pair (L, A), i.e. a Lie algebroid L together with a Lie subalgebroid A, we define the Atiyah class αE of an A-module E as the obstruction to the existence of an A-compatible L-connection on E. We prove that the Atiyah classes αL/A and αE respectively make L/A[−1] and E[−1] into a Lie algebra and a Liealgebra module in the bounded below derived category D+(A), where A is the abelian category of left U(A)-modules and U(A) is the universal enveloping algebra of A. Moreover,we produce a homotopy Leibniz algebra and a homotopy Leibniz module stemming from the Atiyah classes of L/A and E, and inducing the afore said Lie structures in D+(A).