We investigate the Chern–Ricci flow, an evolution equation of Hermitian metrics generalizing the Kähler–Ricci flow, on elliptic bundles over a Riemann surface of genus greater than one. We show that, starting at any Gauduchon metric, the flow collapses the elliptic fibers and the metrics converge to the pullback of a Kähler–Einstein metric from the base. Some of our estimates are new even for the Kähler–Ricci flow. A consequence of our result is that, on every minimal non-Kähler surface of Kodaira dimension one, the Chern–Ricci flow converges in the sense of Gromov–Hausdorff to an orbifold Kähler–Einstein metric on a Riemann surface.

We quantized the full Einstein equations in a globally hyperbolic spacetime $N=N^{n+1}$, $n\ge 3$, and found solutions of the resulting hyperbolic equation in a fiber bundle $E$ which can be expressed as a product of spatial eigenfunctions (eigendistributions) and temporal eigenfunctions. The spatial eigenfunctions form a basis in an appropriate Hilbert space while the temporal eigenfunctions are solutions to a second order ordinary differential equation in $\R[]_+$. In case $n\ge 17$ and provided the cosmological constant $\Lam$ is negative the temporal eigenfunctions are eigenfunctions of a self-adjoint operator $\hat H_0$ such that the eigenvalues are countable and the eigenfunctions form an orthonormal basis of a Hilbert space.

The free-living SAR11 clade is a globally abundant group of oceanic Alphaproteobacteria, with small genome sizes and rich genomic A+T content. However, the taxonomy of SAR11 has become controversial recently. Some researchers argue that the position of SAR11 is a sister group to Rickettsiales. Other researchers advocate that SAR11 is located within free-living lineages of Alphaproteobacteria. Here, we use the natural vector representation method to identify the evolutionary origin of the SAR11 clade. This alignment-free method does not depend on any model assumptions. With this approach, the correspondence between proteome sequences and their natural vectors is one-to-one. After fixing a set of proteins, each bacterium is represented by a set of vectors. The Hausdorff distance is then used to compute the dissimilarity distance between two bacteria. The phylogenetic tree can be reconstructed based on these distances. Using our method, we systematically analyze four data sets of alphaproteobacterial proteomes in order to reconstruct the phylogeny of Alphaproteobacteria. From this we can see that the phylogenetic position of the SAR11 group is within a group of other free-living lineages of Alphaproteobacteria.

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