Patterns of sediment deposition in subsiding coastal salt marshes,Terrebonne Bay,Louisiana: The role of winter storms

High rates of wetland loss in the Mississippi deltaic plain have been attributed to a combination of insufficient marsh sedimentation and relative sea-level rise rates of over 1.2 cm yr^?1. This study examines contemporary patterns of sediment delivery to the marsh surface by evaluating the contribution of individual marsh flooding events. Strong meteorological effects on water level in Terrebonne Bay often mask the usual microtidal fluctuations in water level and cause flood events to be of unpredictable frequency and duration. Sediment deposited on the marsh surface was collected weekly at two sites. Preliminary results allow the relative contributions of tidal and storm inundations to be calculated. Maximum sedimentation is associated with strong southerly winds both causing increased flooding and mobilizing sediment from open bay areas. Sediment deposition is limited by the availability of suspended sediment and the opportunity for its transport onto the marsh surface.     

Quantifying the effects of subsurface heterogeneity on hillslope runoff using a stochastic approach

The role of heterogeneity and uncertainty in hydraulic conductivity on hillslope runoff production was evaluated using the fully integrated hydrologic model ParFlow. Simulations were generated using idealized high-resolution hillslopes configured both with a deep water table and a water table equal to the outlet to isolate surface and subsurface flow, respectively. Heterogeneous, correlated random fields were used to create spatial variability in the hydraulic conductivity. Ensembles, generated by multiple realizations of hydraulic conductivity, were used to evaluate how this uncertainty propagates to runoff. Ensemble averages were used to determine the effective runoff for a given hillslope as a function of rainfall rate and degree of subsurface heterogeneity. Cases where the water table is initialized at the outlet show runoff behavior with little sensitivity to variance in hydraulic conductivity. A technique is presented that explicitly interrogates individual realizations at every simulation timestep to partition overland and subsurface flow contributions. This hydrograph separation technique shows that the degree of heterogeneity can play a role in determining proportions of surface and subsurface flow, even when effective hillslope outflow is seen. This method is also used to evaluate current hydrograph separation techniques and demonstrates that recursive filters can accurately proportion overland and base-flow for certain cases.     

The response of coastal marshes to sea-level rise: Survival or submergence?

In order to maintain an elevation in the intertidal zone at which marsh vegetation can survive, vertical accretion of the marsh surface must take place at a rate at least equal to the rate of relative sea-level rise. Net vertical accretion of coastal marshes is a result of interactions between tidal imports, vegetation and depositional processes. All of these factors are affected, directly or indirectly, by alterations in marsh hydrology which might occur as a result of sea-level rise. The overall response of coastal marshes to relative sea-level rise depends upon the relative importance of the inorganic and organic components of the marsh soil and the impact of increased hydroperiod on net accumulation. The varied combination of factors contributing to sediment supply, and their complexity at the scale of individual marshes, means that predicting the response of suspended sediment concentration in marsh floodwater to any changes which may occur as a result of sea-level rise, at anything other than the local scale is unlikely to be accurate. The impact of sea-level rise on net below-ground production is also complex. The sensitivity of certain species to waterlogging and soil chemical changes could result in a change in species composition or the migration of vegetation zones. Consequently, predicting the net impact of sea-level rise on organic matter accumulation is fraught with difficulties and requires improved understanding of interactions between vegetation, soil and hydrologic processes.     

Time-resolved spectroscopy of the sdBV V338 Serpentis

We obtained 1955 high-resolution spectra of the high-amplitude pulsating subdwarf B star V338 Ser with the FIES spectrograph at the 2.5 m Nordic Optical Telescope covering 4 full nights in May–June 2009. Here we present the first results from phase-folding the data on the main pulsation mode, as revealed by simultaneous B-band photometry obtained with the Mercator 1.25 m and Baker 0.4 m telescopes. We compare the results with a sample line-profile model produced with LTE atmospheres and bruce+kylie.     

Lithium tracer-diffusion in an alkali-basaltic melt — An ion-microprobe determination

An ion-microprobe-based technique has been used to measure lithium tracer-diffusion coefficients (D_Li) in an alkali-basaltic melt at 1300, 1350 and 1400°C. The results can be expressed in the form:D_Li=7.5 ×10^?2exp(?27,600/RT)cm²S^?1The results show significantly faster diffusion rates than those previously recorded for other monovalent, divalent and trivalent cations in a tholeiitic melt. Consequently, diffusive transport of ions acting over a given time in a basaltic melt can produce a wider range of transport distance values than hitherto supposed. Hence, it is concluded that great care should be exercised when applying diffusion data to petrological problems.     

Calculation of multicomponent chemical equilibria and reaction processes in systems involving minerals,gases and an aqueous phase

The compositional characteristics of many geochemical systems which involve the interaction of natural aqueous solutions with minerals and gases are conveniently described using the following thermodynamic components: Cl^?, SO₄⁼, HS^?, CO₃⁼, H⁺, Na⁺, K⁺, Ca⁺⁺, Mg⁺⁺, Fe⁺⁺, Zn⁺⁺, Cu⁺, Al⁺⁺⁺, SiO₂ and H₂O. A set of mass balance and mass action equations equal in number to the number of components plus the number of saturated minerals (and gases) is defined for a specified temperature, pressure and bulk composition. The mass balance equations include terms for minerals, gases and the molalities of aqueous complexes and dissociated species. This set of non-linear equations can be solved with the aid of a computer using'a Newton-Raphson technique. The calculation takes account of aqueous ion complexing, oxidation-reduction equilibria, activity coefficients, non-unit water activity and solid solutions. The use of H⁺, SO₄⁼, HS^? and H₂O as components allows straightforward treatment of processes involving oxidation-reduction, evaporation, boiling and changes of total aqueous H⁺ due to hydrolysis, mineral reaction or temperature change. One product of this approach is a technique for calculating pH at high temperature from measurement of pH at room temperature.By linking a series of discrete overall heterogeneous equilibrium calculations in which incremental changes of bulk composition, temperature or pressure are made, dynamic geochemical processes can be modeled. Example calculations for two such processes are given. These are the heating of seawater from 25° to 300°C and the isothermal irreversible reaction of rhyolite with an aqueous solution at 250°C.