In this note we propose a generalization of heterotic/F-theory duality. We introduce a set of non-compact building blocks which we glue together to reach compact examples of generalized duality pairs. The F-theory building blocks consist of non-compact elliptically fibered Calabi-Yau fourfolds which also admit a K3 fibration. The compact elliptic model obtained by gluing need not have a globally defined K3 fibration. By replacing the K3 fiber of each F-theory building block with a T2, we reach building blocks in a heterotic dual vacuum which includes a position dependent dilaton and three-form flux. These building blocks are glued together to reach a heterotic flux background. We argue that in these vacua, the gauge fields of the heterotic string become localized, and remain dynamical even when gravity decouples. This enables a heterotic dual for the hyperflux GUT breaking mechanism which has recently figured prominently in F-theory GUT models. We illustrate our general proposal with some explicit examples.

We consider a discrete, non-Hermitian random matrix model, which can be expressed as a shift of a rank-one perturbation of an anti-symmetric matrix. We show that, asymptotically almost surely, the real parts of the eigenvalues of the non-Hermitian matrix around any fixed index are interlaced with those of the anti-symmetric matrix. Along the way, we show that some tools recently developed to study the eigenvalue distributions of Hermitian matrices extend to the anti-symmetric setting.

Although random cell complexes occur throughout the physical sciences, there does not appear to be a standard way to quantify their statistical similarities and differences. The various proposals in the literature are usually motivated by the analysis of particular physical systems and do not necessarily apply to general situations. The central concepts in this paper—the swatch and the cloth—provide a description of the local topology of a cell complex that is general (any physical system that can be represented as a cell complex is admissible) and complete (any statistical question about the local topology can be answered from the cloth). Furthermore, this approach allows a distance to be defined that measures the similarity of the local topology of two cell complexes. The distance is used to identify a steady state of a model grain boundary network, quantify the approach to this steady state, and show that the steady state is independent of the initial conditions. The same distance is then employed to show that the long-term properties in simulations of a specific model of a dislocation network do not depend on the implementation of dislocation intersections.

We revisit the “state-dependence” of the map that we proposed recently between bulk operators in the interior of a large AdS black hole and operators in the boundary CFT. By refining recent versions of the information paradox, we show that this feature is necessary for the CFT to successfully describe local physics behind the horizon — not only for single-sided black holes but even in the eternal black hole. We show that state-dependence is invisible to an infalling observer who cannot differentiate these operators from those of ordinary quantum effective field theory. Therefore the infalling observer does not observe any violations of quantum mechanics. We successfully resolve a large class of potential ambiguities in our construction. We analyze states where the CFT is entangled with another system and show that the ER=EPR conjecture emerges from our construction in a natural and precise form. We comment on the possible semi-classical origins of state-dependence.

Most of classical theoretical ecology is based on the assumption that organisms in a community can be naturally partitioned into groups of individuals that can be treated as identical. At the same time, mounting experimental evidence from studies of microbial communities raises the intriguing question whether this intuition is an accurate description of the microbial world. This work builds on Mac Arthur’s model of competitive coexistence on multiple resources to construct a framework that does not rely on postulated existence of species as fundamental ecological variables. In one parameter regime, effective “species” with a core and accessory genome naturally appear in this model as emergent concepts. However, the same model allows a smooth transition to a highly diverse regime where the species formalism becomes inadequate. An alternative description is proposed based on the dynamical modes of population fluctuations. This approach provides a naturally hierarchical description of community dynamics which is well-defined even when the species description breaks down. The relevance of this framework for understanding the complexity of naturally observed microbial communities is discussed.