The dynamical evolution of spatial patterns in a complex system can reveal the underlying structure and stability of stationary states. As a model system we employ a two-component Bose-Einstein condensate at the transition from miscible to immiscible with the additional control of linear interconversion. Excellent agreement is found between the detailed experimental time evolution and the corre...

We characterize the immiscibility-miscibility transition (IMT) of a two-component Bose-Einstein condensate (BEC) with dipole-dipole interactions. In particular, we consider the quasi-two-dimensional geometry, where a strong trapping potential admits only zero-point motion in the trap direction, while the atoms are more free to move in the transverse directions. We employ the Bogoliubov treatmen...

Two occurrences of platinum-group elements (PGEs) along the northern margin of the Skaergaard intrusion include a sulfide-bearing gabbro with slightly less than 1 ppm PGE + Au and a clinopyroxene-actinolite-plagioclase-biotiteilmenite schist with 16 vol% sulfide and 1.8 ppm PGE + Au. Both have assemblages of pyrrhotite, pentlandite, and chalcopyrite typical for orthomagmatic sulfides. Matching ...

We report Monte Carlo simulations that show both vapor-liquid and closed-loop liquid-liquid equilibrium in a pure substance, for a model fluid that forms orientation-dependent intermolecular bonds. This is the first time that direct evidence of liquid-liquid immiscibility in a pure fluid has been found using exact methods. Because the model is formulated in terms of a tetrahedrally coordinated ...

Cell membranes contain a variety of lipid species that differ in their physico-chemical properties. Lipid-lipid immiscibility gives rise to lateral heterogeneities in the membrane plane, a subset of which are termed lipid rafts (Simons and Vaz, 2004). Originally defined biochemically as detergentresistant membrane (DRM) fractions, lipid rafts are proposed to be highly dynamic, submicroscopic as...