Knowledge of the flow patterns within distributary systems is key for understanding deltaic hydro- and morpho-dynamics, yet synoptic measurements of flow fields remain virtually nonexistent. As a means of overcoming this problem, a small number of studies have used biogenic surface films as synoptic flow tracers, under the assumption that biofilm streaklines are tangent to the local flow direction. Here we rigorously test this assumption and show that, despite flow patterns that change severely in space and time (over a range >270°), streaklines are relatively accurate synoptic flow tracers for the Wax Lake Delta, in Louisiana. When the incoming discharge was greater than 2400 m3/s with stable or falling tides, the streakline-derived flow direction departed from near bed flow direction measurements of 22.8° (root mean square). When the discharge was greater than 2400 m3/s and the tides were rising greater than 0.03 m/hr, they were accurate within 28.0°. Under conditions of discharge less than 2400 m3/s and tidal change less than a positive 0.03 m/hr, they were accurate within 33.3°, while during low discharge and rising tides they were accurate within 58.9°. Accuracy varied with distance from the delta, with proximal sites having greater precision. Our results demonstrate that a streakline-derived flow direction can characterize the spatiotemporal variability in the flow directions, but that the accuracy is significantly influenced by the hydrodynamic conditions and location within the network.

We propose an exploratory model to describe the morphodynamics of distributary channel network growth on river deltas. The interface between deep channels and the shallow, unchannelized delta front deposits is modeled as a moving boundary. Steady flow over the unchannelized delta front is friction dominated and modeled by Laplace's equation. Shear stress along the network boundary produces nonlinear erosion rates at the interface, causing the boundary to move and network elements (channels and branches) to form. The model was run for boundary conditions resembling the Wax Lake Delta in coastal Louisiana, 20 parameterizations of sediment transport, and 3 parameterizations of discharge. In each case, the model produced a complex channel network with channel number, width, bifurcation angle, and channel shape depending on the sediment transport formula. For reasonable sediment transport parameters and gradually increasing water discharge, the model produced network characteristics and progradation rates similar to the Wax Lake Delta. This suggests that the model contains the processes responsible for network growth, despite its abstract formulation. Key Points:• Prograding distributary channel networks of varying morphology can be modeled as a simple moving boundary • Nonlinearities in the sediment transport formula dictate channel width, number of branches, bifurcation angle, and channel shape • Evolution is dictated by network morphology, sediment transport, and water discharge Supporting Information:• Supporting Information S1

We have reported that extracts prepared from many human and mouse cell lines show little or no Sp2 DNA-binding activity and that Sp2 has little or no capacity to stimulate transcription of promoters that are activated by Sp1, Sp3, and Sp4. Using an array of chimeric Sp1/Sp2 proteins we showed further that Sp2 DNA-binding activity and trans-activation are each negatively regulated in mammalian cells. As part of an ongoing effort to study Sp2 function and regulation we characterized its subcellular localization in comparison with other Sp-family members in fixed and live cells. We report that 1) Sp2 localizes largely within subnuclear foci associated with the nuclear matrix, and 2) these foci are distinct from promyelocytic oncogenic domains and appear to be stable during an 18-h time course of observation. Deletion analyses identified a 37 amino acid sequence spanning the first zinc-"finger" that is sufficient to direct nuclear matrix association, and this region also encodes a bipartite nuclear localization sequence. A second nuclear matrix targeting sequence is encoded within the Sp2 trans-activation domain. We conclude that Sp2 preferentially associates with the nuclear matrix and speculate that this subcellular localization plays an important role in the regulation of Sp2 function.