Subduction and back-arc activity at the Hikurangi convergent Margin,New Zealand

The Hikurangi Margin is a region of oblique subduction with northwest-dipping intermediate depth seismicity extending southwest from the Kermadec system to about 42°S. The current episode of subduction is at least 16–20 Ma old. The plate convergence rate varies along the margin from about 60 mm/a at the south end of the Kermadec Trench to about 45 mm/a at 42°S. The age of the Pacific lithosphere adjacent to the Hikurangi Trench is not known.The margin divides at about latitude 39°S into two quite dissimilar parts. The northern part has experienced andesitic volcanism for about 18 Ma, and back-arc extension in the last 4 Ma that has produced a back-arc basin onshore with high heaflow, thin crust and low upper-mantle seismic velocities. The extension appears to have arisen from a seawards migration of the Hikurangi Trench north of 39°S. Here the plate interface is thought to be currently uncoupled, as geodetic data indicate extension of the fore-arc basin, and historic earthquakes have not exceededM _s=7.South of 39°S there is no volcanism and a back-arc basin has been produced by downward flexure of the lithosphere due to strong coupling with the subducting plate. Heatflow in the basin is normal. Evidence for strong coupling comes from historic earthquakes of up to aboutM _s=8 and high rates of uplift on the southeast coast of the North Island.The reason for this division of the margin is not known but may be related to an inferred increase, from northeast to southwest, in the buoyancy of the Pacific lithosphere.     

Fractals in Karst

The analysis of cave survey data is used to establish that cave length exhibits fractal (self-similar) behaviour, with dimensions in the range 1–1·5, over a range of measurement resolutions from 1 to 100 m. It is suggested that fractal dimensions, together with their range of applicability, will prove to be useful parameters for the study of caves.     

On the Integrability of Limited-Area Numerical Weather Prediction Model ALADIN over Extended Time Periods

This note summarizes results of the first integration of regional numerical weather prediction model ALADIN in a climate mode. The ALADIN model, developed in an international cooperation led by Météo France, is operationally used for weather prediction. The grid step of the model is 12 km; the integration domain covers a major part of Europe. A one-month-long run has been performed with this model on observed boundary conditions (represented by assimilations by the global model ARPEGE). It is demonstrated that no excessive error is generated and accumulated in the model during the integration; hence the model is integrable for extended time periods and may serve a basis for a development towards a regional climate model.     

Two Experimental Methods to Determine the Speciation of Cadmium in Sediment from the River Neckar

The binding forms of Cd to an anaerobic sediment of low sulfide content from Lauffen reservoir (River Neckar, Germany) were studied using two different approaches, i. e. sequential extraction (modified from published protocols) and titrimetric study of the pH-dependent Cd release. Thermodynamic equilibrium calculations were applied to calculate both the release pattern of Cd during the titrations and the speciation of Cd within the single fractions of the extraction protocol. The calculations were based on measured sediment parameters such as hydrous ferric oxide (HFO), acid volatile sulfide, carbonate content and total Cd content, and the extractants (oxalate, acid etc.) used. The results of the two independent approaches coincided well in that they both assigned more than two thirds of the total Cd content to be adsorbed to organic matter. Cd bound as CdS is of little importance. Sequential extraction after a 3-month oxidation period at pH 7 revealed a shift of Cd from being mainly bound in stronger surface complexes with organic matter to being mainly bound in weaker surface complexes with organic matter and HFO, and thus becoming more bioavailable. This study suggests that the use of sequential extraction although being frequently criticized due to its operational character can be used to determine binding forms of metal ions if they are accompanied by 1) careful supporting experiments, 2) analysis of important sediment parameters, and 3) the use of thermodynamic equlibrium models which can help to understand Cd speciation within the extraction fractions.     

Major element chemistry of Galapagos Rift Zone magmas and their phenocrysts

Basalts dredged from the Galapagos Rift Zone between 85°W and 100°W were analyzed by electron microprobe to determine the chemistry of the glass exteriors and included phenocrysts, microphenocrysts and quench minerals. The basalts come from both “normal” mid-ocean ridge segments and from ridge segments that cross the Galapagos Platform. The basalts fall into two chemical and geographical groups. Group A basalts come from outside the central region of the Galapagos Platform (i.e., outside 89–92.5°W) and are chemically similar to basalts from “normal” ocean ridge segments. Group B basalts come from the center of the Galapagos Platform (89–92.5°W) and are enriched in incompatible elements like “plume-influenced” basalts from the Mid-Atlantic Ridge. The spinel, olivine, plagioclase and clinopyroxene phenocrysts in both groups of basalts are low-pressure, equilibrium phases, but the chemical difference among basalts from within each group indicates high-pressure fractional crystallization is also responsible for the chemical evolution of some of these basalts. Presently, no crystallization or partial melting model can relate the chemistry of the two groups of basalts and the compositional influence of a large-ion-lithophile elements and water-rich mantle beneath the Galapagos Platform is a viable alternate hypothesis. The eruption temperature of magmas from the “normal” ridge segments, as determined by olivine-liquid thermometry is 1217±10°C, suggesting steady-state conditions but on the Galapagos Platform the eruption temperatures are lower and more variable than on the “normal” ridge (1186°C±30°C) suggesting a more complex plumbing system and the absence of a steady-state magma chamber beneath the platform.     

Automatic sampling of stream water during storm events in small remote catchments

In order to study the relationship between water composition and stream flow rate, it is desirable to sample at a frequency related to flow rate, especially during storm events. In a rural catchment of 18 ha near Oxford, the rate of rainfall was found to be linearly related to discharge on the rising limb of the stream hydrograph. A sampling system was therefore designed in which electrical pulses from a tipping-bucket raingauge were used to initiate and control the action of an automatic water sampler. A threshold rainfall intensity is set above which sampling commences. Sampling then continues at regular increments of rainfall until the intensity drops below the threshold, after which sampling occurs at regular intervals during the period that the stream flow reverts to normal. The CMOS electrical circuits which control the sampling also operate a cassette tape recorder which records the time of each tip of the raingauge and operation of the sampler. Since the sytem is designed to impose very little additional load on the battery which powers the water sampler, and can operate unattended for at least a fortnight, it is ideal for use in small, remote catchments. The system has been extended to include measurements of water temperature and could provide other measurements as well.     

Mass and flux distributions from DNAPL zones in sandy aquifers

At three industrial sites in Ontario, New Hampshire, and Florida, tetrachloroethylene (PCE) and trichloroethylene (TCE), released decades ago as dense nonaqueous phase liquids (DNAPLs), now form persistent source zones for dissolved contaminant plumes. These zones are suspended below the water table and above the bottoms of their respective, moderately homogeneous, unconfined sandy aquifers. Exceptionally detailed, depth-discrete, ground water sampling was performed using a direct-push sampler along cross sections of the dissolved-phase plumes, immediately downgradient of these DNAPL source zones. The total plume PCE or TCE mass-discharge through each cross section ranged between 15 and 31 kg/year. Vertical ground water sample spacing as small as 15 cm and lateral spacing typically between 1 and 3 m revealed small zones where maximum concentrations were between 1% and 61% of solubility. These local maxima are surrounded by much lower concentration zones. A spacing no larger than 15 to 30 cm was needed at some locations to identify high concentration zones, and aqueous VOC concentrations varied as much as four orders of magnitude across 30 cm vertical intervals. High-resolution sampling at these sites showed that three-quarters of the mass-discharge occurs within 5% to 10% of the plume cross sectional areas. The extreme spatial variability of the mass-discharge occurs even though the sand aquifers are nearly hydraulically homogeneous. Depth-discrete field techniques such as those used in this study are essential for finding the small zones producing most of the mass-discharge, which is important for assessing natural attenuation and designing remedial options.