Let G=(V,E) be a locally finite graph. Firstly, using calculus of variations, including a direct method of variation and the mountain-pass theory, we get sequences of solutions to several local equations on G (the Schrödinger equation, the mean field equation, and the Yamabe equation). Secondly, we derive uniform estimates for those local solution sequences. Finally, we obtain global solutions by extracting convergent sequence of solutions. Our method can be described as a variational method from local to global.

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We develop the affine sieve in the context of orbits of congruence subgroups of semisimple groups acting linearly on affine space. In particular, we give effective bounds for the saturation numbers for points on such orbits at which the value of a given polynomial has few prime factors. In many cases these bounds are of the same quality as what is known in the classical case of a polynomial in one variable where the orbit consists of the integers. When the orbit is the set of integral matrices of a fixed determinant, we obtain a sharp result for the saturation number, and thus establish the Zariski density of matrices all of whose entries are prime numbers. Among the key tools used are explicit approximations to the generalized Ramanujan conjectures for such groups, and sharp and uniform counting of points on such orbits when ordered by various norms.

In this paper, we show that any compact K\"ahler manifold homotopic to a compact Riemannian manifold with negative sectional curvature admits a K\"ahler-Einstein metric of general type. Moreover, we prove that, on a compact symplectic manifold $X$ homotopic to a compact Riemannian manifold with negative sectional curvature, for any almost complex structure $J$ compatible with the symplectic form, there is no non-constant $J$-holomorphic entire curve $f:\C\> X$.

This paper studies a two-strain SIS epidemic model with a competing mechanism and a saturating incidence rate on complex networks. This type of incidence rate could be used to reflect the crowding effect of the infective individuals. We first obtain the associated reproduction numbers for each of the two strains which determine the existence of the boundary equilibria. Stability of the disease-free and boundary equilibria are further examined. Besides, we also show that the two competing strains can coexist under certain conditions. Interestingly, the saturating incidence rate can have specific effects on not only the stability of the boundary equilibria, but also the existence of the coexistence equilibrium. Numerical simulations are presented to support the theoretical results.