A prototype earthquake warning system for strike-slip earthquakes

A prototype expert system has been developed to provide rapid warning of earthquakes while they are occurring. Warning times of up to 100 seconds will be possible. In the complete system, several accelerometers are distributed at intervals within a few kilometers of a known fault; data are telemetered to a central computer which implements the expert system. The expert system incorporates specific information about the type of fault to be monitored, and includes simple rules for estimating the fault slip, rupture length, and seismic moment, all in real time. If the seismic moment exceeds a preset value, an alarm may be issued. The prototype is designed for deployment on near-surface strike-slip faults such as the San Andreas and has been successfully tested with data from the 1979 Imperial Valley and 1984 Morgan Hill earthquakes. Crucial concepts have also been tested using synthetic data calculated for a model of the 1857 Fort Tejon earthquake. Parkfield, California, could be used as a test site.     

A model for the estimation of water filtration and nutrient regeneration by exposed sandy beaches

Exposed sandy beaches filter huge volumes of sea water daily as a result of wave and tide action. A regression model is developed which predicts the volume of water filtered daily by a beach as a function of tide range, beach slope and sand particle size. From these parameters estimates are also made of intertidal distance, the degree of expansion of the intertidal above the still water tide range by wave action and the average path length through the sand interstices percolated by filtered sea water. An equation is derived relating the degree of mineralisation of organic matter in the filtered sea water to the distance filtered through the sand and the sand particle size. Employing all this information, a simple model is used to estimate the volumes of sea water filtered and the amounts of inorganic nitrogen regenerated by intertidal sandy beaches over a range of physical conditions. The implications of this nutrient generation for the inshore zone are discussed.     

Spectroscopic characterisation and crystal field calculations of varicoloured kyanites from Loliondo, Tanzania

Orange, ochre-coloured, light green and dark blue varieties of kyanite, ideally Al₂SiO₅, from Loliondo, Tanzania, have been characterised by electron microprobe analysis and polarised infrared and optical absorption spectroscopy. All colour varieties show elevated Fe contents of 0.39 to 1.31 wt.% FeO, but Ti contents only in the range of the EMP detection limit. Orange and ochre-coloured crystals have Mn contents of 0.23 and 0.06 wt.% MnO, respectively, the dark blue kyanite contains 0.28 wt.% Cr₂O₃, while the light green sample is nearly free from transition metal cations other than Fe. Polarised infrared spectra reveal OH defect concentrations of 3 to 17 wt.ppm H₂O with structural OH defects partially replacing the O_B (O2) oxygen atoms. Polarised optical absorption spectra show that the colour of all four varieties is governed by crystal field d-d transitions of trivalent cations, i.e. Fe³⁺ (all samples), Mn³⁺ (orange and ochre) and Cr³⁺ (blue kyanite), replacing Al in sixfold coordinated triclinic sites of the kyanite structure. Intervalence charge transfer, the prevalent colour-inducing mechanism in ‘usual’ (Cr-poor) blue kyanites, seems to play a very minor, if any, role in the present samples. Crystal field calculations in both a ‘classic’ tetragonal and in the semiempirical Superposition Model approach, accompanied by distance- and angle-least-squares refinements, indicate that Fe³⁺ preferably occupies the Al4 site, Cr³⁺ prefers the Al1 and Al2 sites, and Mn³⁺ predominantly enters the Al1 site. In each case specific local relaxation effects were observed according to the crystal chemical preferences of these transition metal cations. Furthermore, the high values obtained in the calculations for the interelectronic repulsion parameter Racah B correspond to a high ionic contribution to Me³⁺–O bonding in the kyanite structure. In the particular case of the blue sample, band positions specifically related to the high Racah B value enable this ‘unusual’ type of blue colouration of kyanite solely due to Cr³⁺ cations.     

Design of sediment detention basins: Scaled model experiments and application

Sediment detention basins are implemented on mountain rivers to trap solid material that may aggravate the flooding of downstream settlements.However,retention structures built in the past may unnecessarily retain sediment during non-hazardous flood events,resulting in high maintenance costs and sediment deficit downstream.In addition,the so-called spontaneous self-flushing of previously retained sediment during floods has occasionally been observed.Recent research suggests to design sediment detention basins for controlling sediment passage with a guiding channel across the deposition area upstream of a hybrid barrier.Such barriers consist of a check dam with a slot orifice and an upstream bar screen with a bottom clearance in order to benefit from a combined mechanical-hydraulic retention control.The present paper enhances this pioneering research with the help of new experimental data,including a wide range of sediment mixtures and large wood,as well as variable barrier heights.Improved design criteria are provided regarding the bar screen and the basin storage capacity.The functionality of the enhanced concept for sediment detention is illustrated by a case study on a physical model:the protection of the Villard-Bonnot village(France)against torrential hazards.     

OH defects in forsterite

Polarized FTIR spectra of near endmember forsterite single crystals from Pamir, Tadzikistan show the existence of sharp strongly pleochroic absorption bands in the region of the OH stretching fundamental. Bands centered at 3674/3624, 3647/3598 and 3640/ 3592 cm^-1 are attributed to OH dipoles oriented parallel to [100]. An OH band doublet at 3570/3535 cm^-1 shows both, a strong absorption parallel to [100] and a strong component parallel to [001]. On the basis of the pleochroic scheme and under the assumption of vacancies on Si- and M-sites it is proposed that O1 is partially replaced by OH defects pointing to the vacant Si-site. O3 is donator oxygen of OH dipoles lying near the O3-O1 tetrahedral edge or roughly pointing to a vacant M2-site. Also O2 can act as donator oxygen of an OH group oriented along the O2-O3 edge of a vacant M1 octahedron. The splitting of the bands is explained by the presence of Fe²⁺ in cation sites surrounding the OH defects.