Effect of monochloramine on isolated fulvic acid

Monochloramine is interesting both as a selective oxidant of fulvic acid and as a drinking water disinfectant. In this study, the controlled reaction of aquatic fulvic acid with monochloramine did not result in products detectable by ether extraction-gas chromatography-flame ionization detection techniques. Evidence of a reaction was shown by bleaching of the fulvic acid solution (decreased absorbance at 465 nm) and chlorine substitution. Chlorine-containing products were quantified by the total carbon adsorbable organic halide (TOX) parameter. Bleaching and organic chlorine formation were much less extensive than in the reaction of free chlorine with fulvic acid. Monochloramine was shown to produce an organic chlorine fraction more hydrophilic and with higher molecular size than that produced by chlorine and fulvic acid. Results suggest that monochloramine may be useful tool for the investigation of certain humic functionalities because it reacts rather selectively and to a small extent with aquatic fulvic acid.     

Geochemistry of phonolites and trachytes from the summit region of Mt. Kenya

Two suites of felsic eruptives and intrusives are represented in a set of samples from the summit region of the Plio-Pleistocene volcano, Mt. Kenya. Most of the samples are moderately or strongly undersaturated and have ⁸⁷Sr/⁸⁶Sr initial ratios in the range 0.70360–0.70368 (mean=0.70362). Members of this phonolitic suite are phonolites, nepheline syenites or kenytes and as a group they show a wide variation in TiO₂, FeO, P₂O₅, Sr, Ba, Zr and Nb. The minor and trace element geochemistry reflect variation in the nature of the parental basaltic magmas from which the phonolitic rocks evolved and variation in the crystal fractionation process in individual cases. Crystal fractionation involving plagioclase, alkali feldspar, clinopyroxene, olivine and magnetite is the process by which most of the phonolitic rocks evolved and variation in the relative proportions of these phases in individual cases has led to a broad spectrum of trace and minor element behaviour. The second suite of felsic samples is critically saturated and consists of trachytes showing either slight oversaturation or slight undersaturation with respect to SiO₂. This trachyte suite has lower initial ⁸⁷Sr/⁸⁶Sr ratios (mean=0.70355) and is derived from transitional alkalic basalts by low pressure (crustal) crystal fractionation involving feldspar, clinopyroxene, magnetite and olivine. The range in minor and trace element chemistry observed among the felsic rocks is a consequence of variation in the parental basalts which is related to mantle source variation and to the specific nature of the crystal fractionation process.     

An equivalent layer magnetization model for Australia based on Magsat data

An equivalent layer magnetization model for Australia and adjacent oceanic areas is presented. The model is obtained by linear inversion of Magsat anomaly data measured in the altitude range 325–550 km. The anomaly data set has been isolated from the raw data set by use of models of the core field and very long wavelength external fields, and is internally consistent. Certain major structural features of the Australian continent are geographically associated with magnetization anomalies. A first-order difference is seen between the Tasman Zone and the Precambrian cratonic areas: magnetization anomalies are much more subdued in the former, possibly reflecting a shallowing of the Curie isotherm within the crust. A profile of the vertical integral of magnetization is presented for a crustal section extending from the Gawler Block to the southeast coast. It is shown that the magnetization variations are probably due partly, but not wholly, to depth to Curie isotherm variations; gross magnetization variations among at least three distinct crustal units must be involved.     

Origin of epigenetic calcite in coal from Antarctica and Ohio based on isotope compositions of oxygen,carbon and strontium

Isotopic compositions of oxygen, carbon and strontium of calcite cleats in coal seams of southern Victoria Land, Antarctica, and Tuscarawas County, Ohio, contain a record of the conditions a the time of their formation. The Antarctic calcites (δ ¹⁸O(SMOW) = +9.14 to +11.82%₀) were deposited from waters enriched in ¹⁶O whose isotopic composition was consistent with that of meteoric precipitation at low temperature and high latitude. The carbon of the calcite cleats (δ ¹³C(PDB) = ?15.6 to ?16.9%₀) was derived in part from the coal (δ ¹³C(PDB) = ?23.5 to ?26.7%₀) as carbon dioxide and by oxidation of methane or other hydrocarbon gases. The strontium (${}^{87}\text{Sr}{}^{86}\text{Sr}\text{= 0.71318–0.72392)}$ originated primarily from altered feldspar grains in the sandstones of the Beacon Supergroup.Calcite cleats in the Kittaning No. 6 coal seam of Ohio (δ ¹⁸O(SMOW) = +26.04 to +27.79%₀) were deposited from waters that had previously exchanged oxygen, possibly with marine carbonate at depth. The carbon (δ ¹³C(PDB) = 0.9 to +2.4%₀) is enriched in ¹³C even though that cleats were deposited in coal that is highly enriched in ¹²C and apparently originated from marine carbonates. Strontium in the cleats ($\text{Sr}\text{87}$ 0.71182–0.71260) is not of marine origin but contains varying amounts of radiogenic ⁸⁷Sr presumably derived from detrital Rb-bearing minerals in the adjacent sedimentary rocks. The results of this study suggest that calcite cleats in coal of southern Victoria Land, Antarctica, were deposited after the start of glaciation in Cenozoic time and that those in Ohio precipitated from formation waters derived from the underlying marine carbonate rocks, probably in the recent geologic past.     

Paleohydrologic regimes in the southwestern Great Basin, 0–3.2 my ago,compared with other long records of “gobal” climate

The oxygen-isotope record from fossil foraminifera in deep-sea sediments is commonly used as a proxy for global ice volume. The linkage between δ¹⁸O and ice volume, however, is probably nonlinear. We have developed a simple numerical model of the isotopic response of the oceans to ice-volume change. The major features it simulates are (1) the changing mean isotopic composition of snow as a function of ice volume (colder snow temperatures forced by climate change and higher-elevation accumulation areas imply more negative mean δ¹⁸O); (2) the nonequilibrium isotopic composition of ice sheets (the past history of an ice sheet is integrated into its mean isotopic composition, which introduces a lag of isotopic “ice volume,” i.e., the measured δ¹⁸O record, scaled to ice-volume units, behind true ice volume); (3) selective preservation of isotopically more negative (colder, higher-latitude) ice (this geographic effect can selectively amplify or dampen the isotopic response to the ice-volume signal). We illustrate the response of our model to simple hypothetical ice-volume transitions of ice growth and ice decay. Sensitivity tests are illustrated for all model parameters. The results suggest that oxygen-isotope records reproduce the general patterns of ice-volume change fairly accurately. The foraminiferal isotope record, however, may misrepresent the true amplitude of the ice-volume signal and lag true ice volume by 1000 to 3000 yr.     

The last interglacial ocean

The final effort of the CLIMAP project was a study of the last interglaciation, a time of minimum ice volume some 122,000 yr ago coincident with the Substage 5e oxygen isotopic minimum. Based on detailed oxygen isotope analyses and biotic census counts in 52 cores across the world ocean, last interglacial sea-surface temperatures (SST) were compared with those today. There are small SST departures in the mid-latitude North Atlantic (warmer) and the Gulf of Mexico (cooler). The eastern boundary currents of the South Atlantic and Pacific oceans are marked by large SST anomalies in individual cores, but their interpretations are precluded by no-analog problems and by discordancies among estimates from different biotic groups. In general, the last interglacial ocean was not significantly different from the modern ocean. The relative sequencing of ice decay versus oceanic warming on the Stage 6/5 oxygen isotopic transition and of ice growth versus oceanic cooling on the Stage 5e/5d transition was also studied. In most of the Southern Hemisphere, the oceanic response marked by the biotic census counts preceded (led) the global ice-volume response marked by the oxygen-isotope signal by several thousand years. The reverse pattern is evident in the North Atlantic Ocean and the Gulf of Mexico, where the oceanic response lagged that of global ice volume by several thousand years. As a result, the very warm temperatures associated with the last interglaciation were regionally diachronous by several thousand years. These regional lead-lag relationships agree with those observed on other transitions and in long-term phase relationships; they cannot be explained simply as artifacts of bioturbational translations of the original signals.     

Chemical beneficiation of zircon concentrates in Western Australia

Western Australian zircons are typically brown-strained and inherently tinged with colour so that production of premium grade zircon has required special attention. The brown coating interferes with the separation of zircon from other minerals and adds to the level of impurities, particularly iron, in the product. Even when the stain is removed the zircon's pink-purple hue detracts from its market appeal. Two separate processes for the beneficiation of zircon to premium grade have been evaluated for three typical Western Australian zircon concentrates. One of the processes has been successfully implemented on a commercial scale.     

Early Paleozoic Magmatism and Gold Mineralization in the Northern Aitun, NW China

Abstract This paper discusses the relationships between granitic magmatism and gold mineralization and the exhumation history of the Dapinggou gold deposit in northern Altun, NW China based on the geochronological data, including zircon U‐Pb ages, Rb‐Sr isochron age and ⁴⁰Ar‐³⁹Ar dating and MDD modeling data. The main granitic magmatism age in this area is attained from the ID TIMS U‐Pb geochronology of zircons from the Kuoshibulak granite, the biggest granite in the northern Altun area, which gives a concordant age of 443±5 Ma in the Late Ordovician. Zircon ID TIMS U‐Pb geochronology of the West Dapinggou biotite granite west of the Dapinggou gold deposit gives concordant ages around 485±10 Ma, representing the early stage of Ordovician magmatism. The Rb‐Sr isochron age (487±21 Ma) of 6 quartz inclusion samples from quartz veins in this gold deposit is very close to that of the West Dapinggou granite. MDD modeling of step heating ⁴⁰Ar‐³⁹Ar data of K‐feldspar from the same West Dapinggou biotite granite gives a rapid cooling history from 300°C to 150°C during 200–185 Ma. According to the age data and the geological setting of this area, we conclude that the Dapinggou gold deposit was formed at the early stage of the Early Paleozoic granitic magmatism in northern Altun, and exhumed in the Early Jurassic due to the normal faulting of the Lapeiquan detachment. The Early Paleozoic magmatism may provide heat source and produce geological fluids, which are very important for gold mineralization. Exhumation in the Mesozoic caused the uplift of the deposit towards the ground surface.