
In 1805 Thomas Young derived the relationship between the static forces of a liquid droplet at rest on a solid substrate. As shown in the schematic, the droplet’s contact angle, θ, can be determined by balancing the horizontal solid–liquid and solid–vapor forces and the horizontal component of the liquid–vapor force, determined by the surface tension, γ/v (see Physics Today, February 2007, page 84). However, for more than two centuries, theories yielded unrealistic singularities for stress and strain at the three-phase contact line. That’s because Young’s equation does not account for the vertical, out-of-plane force pulling on the solid substrate, which naturally should be balanced by the substrate’s elastic response. Now, researchers at Yale University and at consumer products manufacturer Unilever have experimentally and theoretically resolved the out-of-plane contributions. Using a confocal fluorescence microscope, the researchers, led by Yale’s Eric Dufresne, laced a 20-micron-thick film of silicone gel with fluorescent beads and measured the deformation due to a water droplet. At equilibrium, a one-micron-high ridge, illustrated in the inset, formed in the gel at the contact line. When the researchers factored the gel’s surface tension and thickness into a linear elastic model, they arrived at a nonsingular theoretical solution for stress that closely fit their experimental data. Their model, however, underestimates the deformations in the solid-liquid contact plane, which they believe are caused by pinning or viscous drag. (E. Jerison et al., Phys. Rev. Lett., in press.)—Jermey N. A. Matthews







Synchronized oscillatory processes in populations of living cells can arise in two ways. In one type of transition, individual cells oscillate out of synchrony at low number density and gradually synchronize as their density is increased. In another type, cells exhibit no oscillations at low density, but above a threshold density they suddenly begin oscillating in synchrony. Biological systems' complexity makes understanding the transition mechanisms a challenge. But now, researchers led by
Soft biological tissue is often subjected to forces that affect the tissue’s geometry, and finite elasticity provides a robust theoretical framework for analyzing the mechanical behavior of those tissues. Although the theory can accommodate anisotropic, nonlinear, and inhomogeneous processes subjected to large stresses and strains, its complexity makes many problems intractable. For growing tissue, though, the slow addition of cells generates shape- or size-changing stresses that are small enough to model successfully (see PHYSICS TODAY, April 2007,
Theorists have long predicted that scattering materials, such as milk and white paint, contain transparent channels that light can pass right through. Ordinarily, very little of the light in an incident beam enters those so-called open channels, and the materials appear opaque. But it should be possible to create a shaped wave that couples more light into the open channels. In fact, Ivo Vellekoop and Allard Mosk of the University of Twente in the Netherlands have done just that. Last year, they demonstrated a method for shaping a light wave, by tuning the relative phases of segments of their beam, so that much of the light transmitted through their scattering sample would be focused to a point. (See PHYSICS TODAY, October 2007,