Abstract: The paradigm for compartment models in epidemiology assumes exponentially distributed incubation and removal times, which is not realistic in actual populations. Commonly used variations with multiple exponentially distributed variables are more flexible, yet do not allow for arbitrary distributions. We present a new formulation, focussing on the SEIR concept that allows to include general distributions of incubation and removal times. We compare the solution to two types of agent-based model simulations, a spatially homogeneous one where infection occurs by proximity, and a model on a scale-free network with varying clustering properties, where the infection between any two agents occurs via their link if it exists. We find good agreement in both cases. Furthermore a family of asymptotic solutions of the equations is found in terms of a logistic curve, which after a non-universal time shift, fits extremely well all the microdynamical simulations. The formulation allows for a simple numerical approach; software in Julia and Python is provided.

Abstract: In this paper we explore a finite volume renormalization scheme that combines three main ingredients: a coupling based on the gradient flow, the use of twisted boundary conditions and a particular asymmetric geometry, that for SU (N) gauge theories consists on a hypercubic box of size l(2) x (Nl)(2), a choice motivated by the study of volume independence in large N gauge theories. We argue that this scheme has several advantages that make it particularly suited for precision determinations of the strong coupling, among them translational invariance, an analytic expansion in the coupling and a reduced memory footprint with respect to standard simulations on symmetric lattices, allowing for a more efficient use of current GPU clusters. We test this scheme numerically with a determination of the A parameter in the SU (3) pure gauge theory. We show that the use of an asymmetric geometry has no significant impact in the size of scaling violations, obtaining a value Lambda((MS) over bar)root 8t(0) = 0.603(17) in good agreement with the existing literature. The role of topology freezing, that is relevant for the determination of the coupling in this particular scheme and for large N applications, is discussed in detail.

Abstract: We present the details and first results of a new strategy for the determination of alpha s(mZ) (ALPHA Collaboration et al. in Phys. Lett. B 807:135571, 2020). By simultaneously decoupling 3 fictitious heavy quarks we establish a relation between the A-parameters of three-flavor QCD and pure gauge theory. Very precise recent results in the pure gauge theory (Dalla Brida and Ramos in Eur. Phys. J. C 79(8):720, 2019; Nada and Ramos in Eur Phys J C 81(1):1, 2021) can thus be leveraged to obtain the three flavour A-parameter in units of a common decoupling scale. Connecting this scale to hadronic physics in 3-flavour QCD leads to our result in physical units, A(3)/MS = 336(12) MeV, which translates to alpha s(m(Z)) = 0.11823(84). This is compatible with both the FLAG average (Aoki et al. in FLAG review 2021. arXiv:2111.09849 [hep-lat]) and the previous ALPHA result (ALPHA Collaboration et al., Phys. Rev. Lett. 119(10):102001, 2017), with a comparable, yet still statistics dominated, error. This constitutes a highly non-trivial check, as the decoupling strategy is conceptually very different from the 3-flavour QCD step-scaling method, and so are their systematic errors. These include the uncertainties of the combined decoupling and continuum limits, which we discuss in some detail. We also quantify the correlation between both results, due to some common elements, such as the scale determination in physical units and the definition of the energy scale where we apply decoupling.