The definition of quasi-local mass for a bounded space-like region in space-time is essential in several major unsettled roblems in general relativity. The quasi-local mass is expected to be a type of flux integral on the boundary two-surface $ \sum = \partial \Omega $ and should be independent of whichever space-like region $\sum $ bounds. An important idea which is related to the Hamiltonian formulation of general relativity is to consider a reference surface in a flat ambient space with the same first fundamental form and derive the quasi-local mass from the difference of the extrinsic geometries. This approach has be taken by Brown-York [4][5] and Liu-Yau [16][17] (see also related works [12], [15], [6], [14], [3], [9], [28], [32]) to define such notions using the isometric embedding theorem into the Euclidean three space. However, there exist surfaces in the Minkowski space whose quasilocal mass is strictly positive [19]. It appears that the momentum information needs to accounted for to reconcile the difference. In order to fully capture this information, we use isometric embeddings into the Minkowski space as references. In this article, we first prove an existence and uniqueness theorem for such isometric embeddings. We then solve the boundary value problem for Jang’s [13] equation as a procedure to recognize such a surface in the Minkowski space. In doing so, we discover new expression of quasi-local mass for a large class of “admissible” surfaces (see Theorem A and Remark 1.1). The new mass is positive when the ambient space-time satisfies the dominant energy condition and vanishes on surfaces in the Minkowski space. It also has the nice asymptotic behavior at spatial infinity and null infinity. Some of these results were announced in [29].

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Adult stem cells, which exist throughout the body, multiply by cell division to replenish dying cells or to promote regeneration to repair damaged tissues. To perform these functions during the lifetime of organs or tissues, stem cells need to maintain their populations in a faithful distribution of their epigenetic states, which are suscepti- ble to stochastic fluctuations during each cell division, unexpected injury, and potential genetic mutations that occur during many cell divisions. However, it remains unclear how the three processes of differentiation, proliferation, and apoptosis in regulating stem cells collectively manage these challenging tasks. Here, without consid- ering molecular details, we propose a genetic optimal control model for adult stem cell regeneration that includes the three fundamental processes, along with cell division and adaptation based on differ- ential fitnesses of phenotypes. In the model, stem cells with a distri- bution of epigenetic states are required to maximize expected performance after each cell division. We show that heteroge- neous proliferation that depends on the epigenetic states of stem cells can improve the maintenance of stem cell distributions to create balanced populations. A control strategy during each cell division leads to a feedback mechanism involving heterogeneous proliferation that can accelerate regeneration with less fluctuation in the stem cell population. When mutation is allowed, apoptosis evolves to maximize the performance during homeostasis after multiple cell divisions. The overall results highlight the importance of cross-talk between genetic and epigenetic regulation and the performance objectives during homeostasis in shaping a desirable heterogeneous distribution of stem cells in epigenetic states.