A numerical model of beach morphological evolution due to waves and currents in the vicinity of coastal structures

A numerical model was developed of beach morphological evolution in the vicinity of coastal structures. The model includes five sub-models for random wave transformation, surface roller development, nearshore wave-induced currents, sediment transport, and morphological evolution. The model was validated using high-quality data sets obtained during experiments with a T-head groin and a detached breakwater in the basin of the Large-scale Sediment Transport Facility at the Coastal and Hydraulics Laboratory in Vicksburg, Miss, USA. The simulations showed that the model reproduced well the wave conditions, wave-induced currents, and beach morphological evolution in the vicinity of coastal structures. Both salient and tombolo formation behind a T-head groin and a detached breakwater were simulated with good agreement compared to the measurements.     

Coupling Between Seismic Activity and Hydrogeochemistry at the Shillong Plateau, Northeastern India

Transient hydrogeochemical anomalies were detected in a granite-hosted aquifer, which is located at a depth of 110 m, north of the Shillong Plateau, Assam, India, where groundwater chemistry is mainly buffered by feldspar alteration to kaolinite. Their onsets preceded moderate earthquakes on December 9, 2004 (M_W = 5.3) and February 15, 2005 (M_W = 5.0), respectively, 206 and 213 km from the aquifer. The ratios [Na+K]/Si, Na/K and [Na+K]/Ca, conductivity, alkalinity and chloride concentration began increasing 3–5 weeks before the M_W = 5.3 earthquake. By comparison with field, experimental and theoretical studies, we interpret a transient switchover between source aquifers, which induced an influx of groundwater from a second aquifer, where groundwater chemistry was dominantly buffered by the alteration of feldspar to smectite. This could have occurred in response to fracturing of a hydrological barrier. The ratio Ba/Sr began decreasing 3–6 days before the M_W = 5.0 earthquake. We interpret a transient switchover to anorthite dissolution caused by exposure of fresh plagioclase to groundwater interaction. This could have been induced by microfracturing, locally within the main aquifer. By comparison with experimental studies of feldspar dissolution, we interpret that hydrogeochemical recovery was facilitated by groundwater interaction and clay mineralization, which could have been coupled with fracture sealing. The coincidence in timing of these two hydrogeochemical events with the only two M_W ≥ 5 earthquakes in the study area argues in favor of cause-and-effect seismic-hydrogeochemical coupling. However, reasons for ambiguity include the lack of similar hydrogeochemical anomalies coupled with smaller seismic events near the monitoring station, the >200 km length scale of inferred seismic-hydrogeochemical coupling, and the potential for far-field effects related to the Great Sumatra–Andaman Islands Earthquake of December 26, 2004.     

Discussion of “Measurements of sheet flow transport in acceleration-skewed oscillatory flow and comparison with practical formulations” by D.A. van der A,T. O'Donoghue and J.S. Ribberink

The authors present a very interesting data set on the acceleration effects on sheet flow transport and compare their experimental results with different transport practical formulas. However, they omit some previous work by Camenen and Larson (2007) that we would like to bring to the authors' attention. A more extensive discussion on some aspects of the acceleration effects is also lacking in their paper and, thus, additional material is provided here.     

A new formula for the total longshore sediment transport rate

A new predictive formula for the total longshore sediment transport (LST) rate was developed from principles of sediment transport physics assuming that breaking waves mobilize the sediment, which is subsequently moved by a mean current. Six high-quality data sets on hydrodynamics and sediment transport collected during both field and laboratory conditions were employed to evaluate the predictive capability of the new formula. The main parameter of the formula (a transport coefficient), which represents the efficiency of the waves in keeping sand grains in suspension, was expressed through a Dean number based on dimensional analysis. The new formula yields predictions that lie within a factor of 0.5 to 2 of the measured values for 62% of the data points, which is higher than other commonly employed formulas for the LST rate such as the CERC equation or the formulas developed by Inman–Bagnold and Kamphuis, respectively. The new formula is well suited for practical applications in coastal areas, as well as for numerical modeling of sediment transport and shoreline change in the nearshore.     

Metop-GRAS in-orbit instrument performance

The GRAS instrument on the Metop-A satellite provides more than 600 radio occultation measurement profiles per day. The instrument is characterized by its wide antenna coverage, high signal-to-noise ratio and an ultra-stable clock reference. The conventional dual-frequency tracking of GPS signals is under dynamic atmosphere conditions complemented by open loop tracking with sampling of the signal at a 1 kHz rate, providing an unprecedented view of the signal spectral environment. This paper presents the instrument performance as derived from analysis of in-orbit measurement data. We show that the noise figure is low enough to enable mapping of external radio noise variations over the earth’s surface. An error propagation model is presented to relate instrument characteristics to bending angle performance. This model is also used to illustrate the relation between filter bandwidth, resolution and measurement noise. The Doppler model, guiding open loop measurements, is found to be accurate to better than 20 Hz with a possibility for improvement to 10 Hz. The high performance at low altitudes enables the presence of surface reflections at the −20-dB level to be identified in more than 50% of the occultations. The potential performance improvements for next generation receivers are discussed.     

Surface Charge Concentrations on Silica in Different 1.0 M Metal-Chloride Background Electrolytes and Implications for Dissolution Rates

The empirical rate laws formulated to describe the dissolution rates of oxide minerals include the surface charge concentration that results from the protonation and deprotonation of surface functional groups. Previous experiments on quartz and silica have shown that dissolution rates vary as a function of different background electrolyte solutions, however, such experiments are often conducted at elevated temperatures where it is difficult to estimate surface charge along with the dissolution rates. In the present study we measuresurface charge concentrations for silica in different electrolyte solutions at 298 K in order to quantify the extent to which the different counterions could affect the dissolution rates through their influence on the surface charge concentrations. The experimental solutions in the electrolyte series: LiCl, NaCl, KCl, RbCl, CaCl₂, SrCl₂ and BaCl₂ were prepared to maintain a constant metal concentration of 1.0 M. For the alkali-metal chlorides, the surface charge concentrations correlate with the size of the hydrated alkali metal, consistent with the idea that these counterions affect charge via outer-sphere coordination that shield proton surface complexes from one another. The reactivity trend for alkaline-earth cations is less clear, but the data demonstrate distinct differences in the acid-base propertiesof the silica surface in these different electrolytes. We then discuss how these trends are manifested in the rate equations used to interpret dissolution experiments.     

Chemical Weathering Rates, Erosion Rates and Mobility of Major and Trace Elements in a Boreal Granitic Till

Chemical weathering rates and erosionrates of granitic till in northern Sweden have beenestimated. The present-day chemical weathering rate iscompared with the long-term average weathering ratesince the last deglaciation approximately 8,700 yearsago. Also, the present-day release rates of major andtrace elements due to chemical weathering are comparedwith the mobility of these elements in a spodosolprofile as shown by soil water samples from the vadozezone. The estimation of the past weathering rate isbased on elemental depletion trends in a soil profile(typic haplocryod), whereas the present weatheringrate is based on elemental input/output budgets in asmall catchment (9.4 km²). The long-term averagechemical erosion rate, expressed as the sum of majorelement oxides (SiO₂, Al₂O₃, CaO,Fe₂O₃, K₂O, MgO, MnO, Na₂O,P₂O₅, TiO₂), was estimated to be4.9 gm^-2 yr^-1. The long-term base cation(Ca²⁺, Mg²⁺, Na⁺, K⁺) depletionwas 0.325 keq ha^-1 yr^-1. The currentchemical erosion rate was estimated to be2.43.0 g ^-2 yr^-1, which is at least an order ofmagnitude higher than the rate of physical erosion,and the base cation flux due to chemical weathering is0.356–0.553~keq ha^-1 yr^-1. However,0.074 keq ha^-1 yr^-1 of this flux may be related tocation exchange processes induced by atmospheric inputof acid rain. There is no evidence for any recentlyincreased weathering rate of silicates in this area.The inputs of Cd, Cu, Ni and Zn exceed the outputs,and hence, these elements are currently accumulatingin the soil.There is a distinct seasonal variation in thechemical composition of the soil water. Results fromthe soil water samples show that Na, followed by Siand S (Cl was not measured), are the most mobileelements in the spodosol profile between the E-horizonand the C-horizon, and that Al and Fe were the leastmobile elements. However, there is no simplerelationship between the mobility of an element in thespodosol profile and the current release rate due toweathering of that element. This fact may haveimplications for the validity of the comparisonbetween the past and present weathering rates asperformed in this study.