Silica Springs,Tongariro National Park,New Zealand—analyses of the spring water and characterisation of the alumino-silicate deposit     

N. Wells  C.W. Childs  C.J. Downes 《Geochimica et cosmochimica acta》1977,41(10):1497-1506

The creamy-white deposit in the stream bed below Silica Springs outlet on Mount Ruapehu, Tongariro National Park, New Zealand, has been identified as a hydrous, X-ray-amorphous, aluminosilicate (allophane). The SiO₂/Al₂O₃ mole ratio varies from close to one, to close to two. The elements K, Ca, Mn and Fe are present in low concentrations relative to those in allophanic soil clays, and tend to increase in concentration downstream from where the deposit first occurs. The concentration of S decreases downstream from 0.5% to 0.1%. Surface areas of samples, measured by the ethylene glycol desorption method, are about 200–300 m²/g. The outlet water at Silica Springs contains low dissolved solids and is undersaturated with respect to amorphous silica, but is supersaturated with respect to several alumino-silicate minerals (of which allophane may be considered the precursor) and with respect to CO₂. Gas bubbling at the outlet contains about 10% CO₂ which has a δC¹³_PDB value of ?7.5%..Silica Springs water is derived from the addition of geothermal CO₂ (and possibly H₂S) to near-surface meteoric water from the lava flow above the outlet, and the chemical attack of this water on the andesitic rocks and soil through which it passes. The pH of water at Silica Springs increases from 5.45 at the outlet, to 5.90 where deposition first occurs, to 6.80 below the region of maximum deposition. This rise in pH correlates with loss of excess CO₂ in turbulent regions of the stream, and, through surface charge effects, is probably an important influence on the site of deposition, which begins approx. 100m downstream from the outlet.  相似文献   

Cleaning of lake sediment samples for diatom oxygen isotope analysis   总被引：1，自引：0，他引：1  

David W. Morley  Melanie J. Leng  Anson W. Mackay  Hilary J. Sloane  Patrick Rioual  Richard W. Battarbee 《Journal of Paleolimnology》2004,31(3):391-401

Detrital grain contamination in a diatom sample can considerably influence the δ¹⁸O_diatom signal. In order to obtain a meaningful signal, pure samples must be used. This can be achieved via a series of cleaning stages including organic and carbonate material removal, sieving, differential settling and heavy liquid separation. The method described here works best for sediments with >20% diatom content. Based on testing various clean-up methods, we propose a sequence of four clean-up stages to produce pure diatom samples from a range of lake sediments types starting with a few grams of sediment. The diatom content and the oxygen isotope composition of the samples at each stage were measured in order to assess the effect of differential amounts of contamination. Results show that a four stage clean-up is necessary to produce clean diatom samples and that contamination by silt and clay causes lower δ¹⁸O values.  相似文献   

Lower crustal granulite xenoliths from the Pannonian Basin,Hungary. Part 1: mineral chemistry,thermobarometry and petrology   总被引：1，自引：0，他引：1  

Antal Embey-Isztin  Hilary Downes  Pamela D. Kempton  Gábor Dobosi  Matthew Thirlwall 《Contributions to Mineralogy and Petrology》2003,144(6):652-670

  相似文献   

Small-scale variations of 87Sr/86Sr isotope composition of barite in the Madjarovo low-sulphidation epithermal system, SE Bulgaria: implications for sources of Sr, fluid fluxes and pathways of the ore-forming fluids     

Peter Marchev  Hillary Downes  Matthew F. Thirlwall  Robert Moritz 《Mineralium Deposita》2002,37(6-7):669-677

  相似文献   

Yerranderie a Late Devonian Silver–Gold–Lead Intermediate Sulfidation Epithermal District, Eastern Lachlan Orogen, New South Wales, Australia     

Peter M. Downes 《Resource Geology》2007,57(1):1-23

Felsic volcanic units of the Early Devonian Bindook Volcanic Complex host the Yerranderie epithermal silver–gold–lead district 94 km west–southwest of Sydney. Mineralization in the district forms part of a fault‐controlled, intermediate sulfidation, epithermal silver–gold–base metal vein system that has significant mineral and alteration zonation. Stage 1 of the mineral paragenesis in the veins developed quartz and carbonate with early pyrite, whereas stage 2 is a crustiform banded quartz–pyrite–arsenopyrite assemblage. Stage 3, the main stage of sulfide deposition, comprises early sphalerite, followed by a tetrahedrite–tennantite–gold assemblage, then a galena–chalcopyrite–native silver–pyrite assemblage, and finally a pyrargyrite–polybasite–pearceite assemblage. Stage 4 involves the deposition of quartz veins with minor (late) pyrite and stage 5 is characterized by siderite that infilled remaining voids. Mineral zonation occurs along the Yerranderie Fault, with bornite being restricted to the Colon Peaks–Silver Peak mine area, whereas arsenopyrite, which is present in both the Colon Peaks–Silver Peak and Wollondilly mine areas, is absent in other lodes along the Yerranderie Fault. The Yerranderie Fault, which hosts the major lodes, is surrounded by a zoned alteration system. With increasing proximity to the fault the intensity of alteration increases and the alteration assemblage changes from an outer quartz–muscovite–illite–(ankerite) assemblage to a quartz–illite–(pyrite–carbonate) assemblage within meters of the fault. ⁴⁰Ar/³⁹Ar dating of muscovite from the alteration zone gave a 372.1 ± 1.9 Ma (Late Devonian) age, which is interpreted to be the timing of the quartz–sulfide vein formation. Sulfur isotope values for sulfides range from 0.1 to 6.2‰ with one outlier of ?5.6 δ³⁴S‰. The results indicate that the initial ore‐forming fluids were reduced, and that sulfur was probably sourced from a magmatic reservoir, either as a direct magmatic contribution or indirectly through dissolution and recycling of sulfur from the host volcanic sequence. The sulfur isotope data suggest the system is isotopically zoned.  相似文献   

U-Th-Pb and Lu-Hf isotopic constraints on the evolution of sub-continental lithospheric mantle, French Massif Central     

Nadine Wittig  Joel A. Baker  Hilary Downes 《Geochimica et cosmochimica acta》2007,71(5):1290-1311

We have carried out a Pb double-spike and Lu-Hf isotope study of clinopyroxenes from spinel-facies mantle xenoliths entrained in Cenozoic intraplate continental volcanism of the French Massif Central (FMC). U-Th-Pb and Lu-Hf isotope systematics verify the existence of different lithospheric domains beneath the northern and southern FMC. Northern FMC clinopyroxenes have extreme Lu/Hf ratios and ultra-radiogenic Hf (ε_Hf = +39.6 to +2586) that reflect ∼15-25% partial melting in Variscan times (depleted mantle model ages ∼360 Ma). Zr, Hf and Th abundances in these clinopyroxenes are low and unaffected by hydrous/carbonatitic metasomatism that overprinted LILE and light REE abundances and caused decoupling of Lu/Hf-Sm/Nd ratios and Nd-Hf isotopes (ε_Nd = +2.1 to +91.2). Pb isotopes of northern FMC clinopyroxenes are radiogenic (²⁰⁶Pb/²⁰⁴Pb > 19), and typically more so than the host intraplate volcanic rocks. ²³⁸U/²⁰⁴Pb ratios range from 17 to 68, and most samples have distinctively low ²³²Th/²³⁸U (<1) and ²³²Th/²⁰⁴Pb (3-22). Clinopyroxenes from southern FMC lherzolites are generally marked by overall incompatible trace element enrichment including Zr, Hf and Th abundances, and have Pb isotopes that are similar to or less radiogenic than the host volcanic rocks. Hf isotope ratios are less radiogenic (ε_Hf = +5.4 to +41.5) than northern FMC mantle and have been overprinted by silicate-melt-dominated metasomatism that affected this part of FMC mantle. Major element and Lu concentrations of clinopyroxenes from southern FMC harzburgites are broadly similar to northern FMC clinopyroxenes and suggest they experienced similar degrees of melt extraction as northern FMC mantle. ²³⁸U/²⁰⁴Pb (53-111) and ²³²Th/²⁰⁴Pb ratios (157-355) of enriched clinopyroxenes from the southern FMC are extreme and significantly higher than the intraplate volcanic rocks. In summary, mantle peridotites from different parts of the FMC record depletion at ∼360 Ma during Variscan subduction, followed by differing styles of enrichment. Northern FMC mantle was overprinted by a fluid/carbonatitic metasomatic agent that carried elements like U, Pb, Sr and light REE. In contrast, much of the southern FMC mantle was metasomatised by a small-degree partial silicate melt resulting in enrichment of all incompatible trace elements. The extreme mantle ²³⁸U/²⁰⁴Pb (northern and southern FMC), ²³²Th/²³⁸U (northern FMC) and ²³²Th/²⁰⁴Pb ratios (southern FMC), coupled with unremarkable present-day Pb isotope ratios, constrain the timing of enrichment. Mantle metasomatism is a young feature related to melting of the upwelling mantle responsible for Cenozoic FMC volcanism, rather than subduction-related metasomatism intimately associated with mantle depletion during the Variscan orogeny. The varying metasomatic styles relate to pre-existing variations in the thickness of the continental lithospheric lid, which controlled the extent to which upwelling mantle could ascend and melt. In the northern FMC, a thicker and more refractory lithospheric lid (?80 km) only allowed incipient degrees of melting resulting in fluid/carbonatitic metasomatism of the overlying sub-continental lithospheric mantle. The thinner lithospheric lid of the southern FMC (?70 km) allowed larger degrees of melting and resulted in silicate-melt-dominated metasomatism, and also focused the location of the volcanic fields of the FMC above this region.  相似文献   

The late-glacial and early-Holocene palaeoecology of cladoceran microfossil assemblages at Kråkenes, western Norway, with a quantitative reconstruction of temperature changes   总被引：2，自引：0，他引：2  

Catherine A. Duigan  Hilary H. Birks 《Journal of Paleolimnology》2000,23(1):67-76

Cladoceran microfossil remains were analysed from a sediment core taken from a lake basin at Kråkenes, western Norway. The sequence included immediate post-glacial conditions (ca. 12,300 ¹⁴C BP), the Allerod, Younger Dryas, and early Holocene to approximately 8,500 ¹⁴C BP. The interpretation of changes in the cladoceran assemblages is based on the known ecology of the taxa, the documented environmental history of the study sequence, the variations in the organic content of the sediment, the radiocarbon dates, and the results of analyses of other biotic groups, including diatoms, macrophytes, and chironomids. In addition, a quantitative reconstruction of changes in air temperature is presented for the study period. This reconstruction is based on transfer functions developed from a separate Swiss surface-sediment cladoceran data set.The cladoceran assemblages throughout the sequence are dominated by littoral chydorid taxa. Bosmina, Daphnia, and Simocephalus represent the open-water component of the zooplankton. Chydorus piger and Daphnia were the only immediate post-glacial pioneer taxa. A rapid proliferation of the open-water and littoral cladoceran taxa began with the onset of the Allerod and persisted for approximately 1,000 yrs. At the start of the Younger Dryas a local glacier formed and drained into the lake, causing a sudden decline in chydorid diversity, with only Chydorus sphaericus and Acroperus harpae persisting throughout this period. Chydorid diversity started to recover in the upper Younger Dryas and continued in the early Holocene. Progressive acidification and oligotrophication are also discernible from the cladoceran assemblages present in the Holocene.The reconstructed mean summer air temperature was from 8-21 °C, with prediction errors of 1.8-2.5 °C. The Allerod was only slightly warmer than the Younger Dryas period, but a progressive increase in temperature is apparent during the early Holocene. In conclusion, the results of this study provide a further demonstration of the value of cladocera as indicators of a variety of palaeoenvironmental parameters, including temperature.  相似文献