Spontaneously propagating cracks in solids emit both pressure and shear waves. When a shear crack propagates faster than the shear wave speed of the material, the coalescence of the shear wavelets emitted by the near-crack-tip region forms a shock front that significantly concentrates particle motion. Such a shock front should not be possible for pressure waves, because cracks should not be able to exceed the pressure wave speed in isotropic linear-elastic solids. In this study, we present full-field experimental measurements of dynamic shear cracks in viscoelastic polymers that result in the formation of a pressure shock front, in addition to the shear one. The apparent violation of classic theories is explained by the strain-rate-dependent material behavior of polymers, where the crack speed remains below the highest pressure wave speed prevailing locally around the crack tip. These findings have important implications for the physics and dynamics of shear cracks such as earthquakes.

Fluids are known to trigger a broad range of slip events, from slow, creeping transients to dynamic earthquake ruptures. Yet, the detailed mechanics underlying these processes and the conditions leading to different rupture behaviors are not well understood. Here, we use a laboratory earthquake setup, capable of injecting pressurized fluids, to compare the rupture behavior for different rates of fluid injection, slow (megapascals per hour) versus fast (megapascals per second). We find that for the fast injection rates, dynamic ruptures are triggered at lower pressure levels and over spatial scales much smaller than the quasistatic theoretical estimates of nucleation sizes, suggesting that such fast injection rates constitute dynamic loading. In contrast, the relatively slow injection rates result in gradual nucleation processes, with the fluid spreading along the interface and causing stress changes consistent with gradually accelerating slow slip. The resulting dynamic ruptures propagating over wetted interfaces exhibit dynamic stress drops almost twice as large as those over the dry interfaces. These results suggest the need to take into account the rate of the pore-pressure increase when considering nucleation processes and motivate further investigation on how friction properties depend on the presence of fluids.

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