NONLINEAR COMPLEX RESISTIVITY OF SOME NICKEL SULPHIDES FROM WESTERN AUSTRALIA*

The electrochemical transfer characteristics of nickel sulphides from six West Australian localities are examined by the nonlinear complex resistivity (nlcr ) method. Ores are classified on the basis of their state of oxidation (supergene, transition zone and primary ores) in an equivalent mine water electrolyte; evidence is found for a systematic change of electrical response with oxidation that is symptomatic of electrochemical reactions varying from diffusion to charge-transfer controlled processes. The analysis is based on the assumption that the Randies’ circuit is an effective model of a rock's electrical response in its natural electrolyte. Both complex impedance plane graphs and computer inversion are used to study the model. Harmonic distortion is a useful aid in this interpretation.     

Experimental diffusion of hydrogen into synthetic fluid inclusions in quartz

Abstract Quartz-hosted, synthetic CO₂-H₂O fluid inclusions behave as open systems with respect to diffusional transfer of hydrogen during laboratory-simulated metamorphic re-equilibration at 650, 750 and 825°C and 1.5 kbar total pressure with f_O2 defined by the C-CH₄ buffer. Microthermometry and Raman spectroscopy show that the initial CO₂-H₂O inclusions become CO₂-CH₄-H₂-H_2O
inclusions after diffusive influx of hydrogen from the reducing confining medium. Measurable changes are observed in inclusion compositions after only 15 days of re-equilibration, implying significant hydrogen mobility at still lower temperatures over geological time spans. Results of synthetic inclusion re-equilibrium experiments have profound implications for the interpretation of natural fluid-inclusion data; failure to account for potential hydrogen migration in inclusions from high-temperature geological environments may lead to erroneous estimates of P-T, and/or the compositions of metamorphic fluids.     

Geochemical Constraints on the Origin of Volcanic Rocks from the Andean Northern Volcanic Zone, Ecuador

Whole-rock geochemical data on basaltic to rhyolitic samplesfrom 12 volcanic centers are used to constrain the role of continentalcrust in the genesis of magmas formed beneath the anomalouslywide subduction-related volcanic arc in Ecuador. Relativelyhomogeneous, mantle-like, isotopic compositions across the arcimply that the parental magmas in Ecuador were produced largelywithin the mantle wedge above the subduction zone and not byextensive melting of crustal rocks similar to those upon whichthe volcanoes were built. Cross-arc changes in ¹⁴³Nd/¹⁴⁴Nd and7/4Pb are interpreted to result from assimilation of geochemicallymature continental crust, especially in the main arc area, 330–360km from the trench. Mixing calculations limit the quantity ofassimilated crust to less than 10%. Most andesites and dacitesin Ecuador have adakite-like trace element characteristics (e.g.Y <18 ppm, Yb <2 ppm, La/Yb >20, Sr/Y >40). Availablewhole-rock data do not provide a clear basis for distinguishingbetween slab-melting and deep crustal fractionation models forthe genesis of Ecuador adakites; published data highlightinggeochemical evolution within individual volcanoes, and in magmaticrocks produced throughout Ecuador since the Eocene, appear tosupport the deep fractionation model for the genesis of mostevolved Ecuadoran lavas. A subset of andesites, which displaya combination of high Sr (>900 ppm), Nd >4·1 and7/4Pb <6·0, appear to be the best candidates amongEcuador lavas for slab-melts associated with the subductionof the relatively young, over-thickened, oceanic crust of theCarnegie Ridge. KEY WORDS: andesite; Ecuador; trace elements; isotopes; adakite     

QUANTIFYING AND MITIGATING FLOOD RISK IN RAPIDLY AGGRADING FLUVIAL SYSTEMS

ILOWERGUADALUPERIVER,SANJOSECALIFORNIATheLowerGuadalupeRiverProjectAreadoesnothavetheabilitytoconveytheflowofthe100-yearfloodevent.LocatedbetweentheSanrranciscoBayandDowntownSanJose,theLowerGuadalupeRiverProjectareaissubjecttomanynaturalandman-inducedagentsandnaturalphysicalprocessesthataffectthehydraulicandsedimenttransportcharacteristicsoftheRiver.Themostsignificantagentsandprocessesincludethelocalgeology,regionalseismicity,tidalprocesses,pastsubsidenceintheregion,risings…     

Fuzzy information representation and processing in conventional GIS software: database design and application

Currently used methods for representing geographical information are inadequate because they do not tolerate imprecision. This leads to information loss and inaccuracy in analysis. Such expressive inadequacy is largely due to the underlying membership concept of classical set theory. To improve information processing in GIS research and application, an alternative membership concept is required. In this paper, we explore the inadequacy imposed upon geographical information representation by classical set theory and address the problems of information loss. A fuzzy relational data model is defined which is more representative for geographical information. A GIS database for agricultural land resource management is created by using the data model and a new technique for assessing land suitability is developed. The fuzzy representation largely facilitates data analysis in this GIS. The methods are tested with data from North Java, Indonesia using a vector-based GIS software package, Arc Info, and the analysis results are presented.     

Cenozoic temperate and sub‐tropical carbonate sedimentation on an oceanic volcano – Chatham Islands,New Zealand

The Chatham Islands, at the eastern end of the Chatham Rise in the South‐west Pacific, are the emergent part of a Late Cretaceous to Cenozoic stratovolcano complex that is variably covered with limestones and fossiliferous tuffs. Most of these deposits accumulated in relatively shallow, high‐energy, tide‐influenced palaeoenvironments with deposition punctuated by periods of deeper‐water pelagic accumulation. Carbonate components in these neritic deposits are biogenic and dominated by molluscs and bryozoans – a heterozoan assemblage. The widespread Middle to Late Eocene Matanginui Limestone contains local photozoan elements such as large benthonic foraminifera (especially Asterocyclina) and calcareous green algae, reflecting the general Palaeogene sub‐tropical oceanographic setting. More localized Late Eocene to Oligocene deposits (Te One Limestone) as well as Pliocene carbonates (Onoua Limestone) are, however, wholly heterozoan and confirm a generally cooler‐water oceanographic setting, similar to today. Early sea floor diagenesis is interpreted to have removed most aragonite components (infaunal bivalves and epifaunal gastropods). Lack of aragonite resulted in the absence of intergranular calcite cementation during subaerial exposure, such that most carbonates are friable or unlithified. Cementation is, however, present at nodular hardground–firmground caps to metre‐scale cycles. Such cements are microcrystalline or micrometre‐thick isopachous circumgranular rinds with insufficient definitive attributes to pinpoint their environment of formation. The overall palaeoenvironment of deposition is interpreted as mesotrophic, resulting in part from upwelling about the Chatham volcanic massif and in part from nutrient element delivery from the adjacent volcanic terrane and coeval volcanism. Biotic diversity in tuffs is two to three times that in limestones, supporting the notion of especially high nutrient availability during periods of volcanism. These mid‐latitude deposits are strikingly different from their low‐latitude, tropical, photozoan counterparts in the volcanic island–coral reef ecosystem. Ground water seepage and fluvial runoff attenuate coral growth and promote microbial carbonate precipitation in these warm‐water settings. In contrast, nutrients from the same sources feed the system in the Chatham Islands cool‐water setting, promoting active heterozoan carbonate sedimentation.     

Analysis of Standard Reference Materials for Zr,Nb, Hf and Ta by ICP-MS after Lithium Metaborate Fusion and Cupferron Separation*

Results are presented of the determination of Zr, Nb, Hf and Ta in 74 standard reference materials by inductively coupled plasma mass spectrometry (ICP-MS). Samples are decomposed by fusion with lithium metaborate and the analytes are separated prior to analysis by precipitation of their cupferrates. Calibration is made using synthetic solutions and internal standardization with Ru (for Zr and Nb) and Re (for Hf and Ta). Accuracy is assessed by comparison with recommended values and precision is evaluated by replicate analyses of five SRMs.