Crystal size distribution in Jurassic Ferrar flows and sills (Victoria Land,Antarctica): evidence for processes of cooling,nucleation, and crystallisation

 Jurassic Ferrar rocks in Victoria Land (Antarctica) occur predominantly as basaltic or andesitic flows and sills. Both show characteristic petrographical and chemical variations, which can be related to in-situ differentiation processes. Such characteristics have been investigated at one flow (“Colonnade flow”) and one sill (“Thumb Point sill”) in the Prince Albert Mountains (Central Victoria Land) based on a statistical grain size analysis and the application of the crystal size distribution theory. A third magma body (“HiTi-unit”), which in previous literature was described as a flow, does not show clear similarities to either the flow or sill. Sill and flow are in-situ differentiated with accumulation of silicic residual melt in the latest cooled parts. For the flow this part is located in the lower half and for the sill in the upper third of their thickness. Thumb Point sill additionally shows an accumulation zone of olivine in the lower third. The position of the residual melt accumulation zone is an indicator for an origin as flow or sill. The HiTi-unit, by contrast, exhibits, only moderate petrographical and chemical variations. Growth and nucleation rates have been determined using, with some modifications, the CSD theory introduced by Marsh (1988). Growth rates of plagioclase for the flow vary from 10⁻¹¹ to 10⁻¹⁰ cm/s and are comparable with literature values for basaltic lava lakes on Hawaii. Nucleation rates vary from 10⁻⁴ to 10⁻³ cm⁻³s⁻¹, which are generally smaller than for Hawaiian basalts. Growth and nucleation rates for the sill cover a large range from 10⁻¹³ to 10⁻¹¹ cm/s and 10⁻⁹ to 10⁻³ cm⁻³s⁻¹, respectively. Systematic variations of these parameters with vertical position were obtained for the sill with its extensive differentiation history. Nucleation and growth rates are dependant on the mode of cooling. Nevertheless, small but significant differences between the flow and sill exist. Growth and nucleation rates of HiTi-unit (10⁻¹² to 10⁻¹¹ cm/s and 10⁻⁶ to 10⁻⁵ cm⁻³s⁻¹) are intermediate between the flow and sill and thus do not allow a distinction of emplacement mode. Received: 6 December 1995 / Accepted: 3 May 1996     

Stand structure and productivity of the introducedRhizophora mangle in Hawaii

Since its introduction in the early part of this century,Rhizophora mangle L. has spread extensively through most of the main islands of the Hawaiian Archipelago. We investigated the structural properties and estimated productivity of aR. mangle population at Nuupia Ponds Wildlife Management Area (NPWMA), on windward Oahu, where the mangroves were being controlled due to their propensity to overgrow archaeological sites and the habitat of endangered Hawaiian waterbirds. Mangroves within NPWMA were very dense (>24,000 trees ha⁻¹) and most were relatively small (only 3.3% of the trees were ≥10 cm DBH). Mean basal area, aboveground biomass, and number of seedlings were all high, at 37.2 m² ha⁻¹, 279 t (dry wt) ha⁻¹, and 121 m⁻², respectively. The seedling, density may be particularly unusual and appears to be due to extremely high rates of propagule, production coupled with low rates of propagule predation. Stand productivity was estimated by stem growth (allometry), litterfall, and a light attenuation approach to determining net canopy photosynthetic production. All three methods yielded estimates that are higher than previously, reported forR. mangle and comparable with estimates of highly productiveRhizophora spp.-dominated stands in Australia and Asia. The high density, biomass, and productivity of this stand relative to stands within the species' native range may be due to a combination of favorable site conditions, lack of competition from other woody plants, and very low rates of herbivory and propagule predation.     

Os-Os systematics of Hawaiian picrites revisited: New insights into Os isotopic variations in ocean island basalts

Eighteen picrites (MgO > 13 wt.%) and three related basalts from six Hawaiian volcanoes were analyzed for ¹⁸⁷Os/¹⁸⁸Os and ¹⁸⁶Os/¹⁸⁸Os. Variations in these ratios reflect long-term Re/Os and Pt/Os differences in the mantle source regions of these volcanoes. ¹⁸⁷Os/¹⁸⁸Os ratios vary from ∼0.129 to 0.136, consistent with the range defined by previous studies of Hawaiian picrites and basalts. Samples with lower ¹⁸⁷Os/¹⁸⁸Os are mainly from Kea trend volcanoes (Mauna Kea and Kilauea), and the more radiogenic samples are mainly from Loa trend volcanoes (Mauna Loa, Hualalai, Koolau and Loihi). As previously suggested, differences in ¹⁸⁷Os/¹⁸⁸Os between volcanic centers are most consistent with the presence of variable proportions of recycled materials and/or pyroxenitic components in the Hawaiian source.¹⁸⁶Os/¹⁸⁸Os ratios vary from 0.1198332 ± 26 to 0.1198480 ± 20, with some samples having ratios that are significantly higher than current estimates for the ambient upper mantle. Although the range of ¹⁸⁶Os/¹⁸⁸Os for the Hawaiian suite is consistent with that reported by previous studies, the new data reveal significant heterogeneities among picrites from individual volcanoes. The linear correlation between ¹⁸⁷Os/¹⁸⁸Os and ¹⁸⁶Os/¹⁸⁸Os reported by a previous study is no longer apparent with the larger dataset. The postulated recycled materials and pyroxenites responsible for the dominant variations in ¹⁸⁷Os/¹⁸⁸Os are likely not responsible for the variations in ¹⁸⁶Os/¹⁸⁸Os. Such materials are typically characterized by both insufficiently high Os concentrations and Pt/Os to account for the ¹⁸⁶Os/¹⁸⁸Os heterogeneities. The lack of correspondence between ¹⁸⁶Os/¹⁸⁸Os variations and the Kea and Loa trends supports this conclusion.The primary cause of ¹⁸⁶Os/¹⁸⁸Os variations are evaluated within the framework of two mixing scenarios: (1) metasomatic transport of Pt and/or ¹⁸⁶Os-rich Os into some portions of the Hawaiian source, and (2) interaction between an isotopically complex plume source with a common, Os- and ¹⁸⁶Os-enriched reservoir (COs). Both scenarios require large scale, selective transport of Pt, Re and/or Os. Current estimates of HSE concentrations in the mantle source of these rocks, however, provide little evidence for either process, so the dominant cause of the ¹⁸⁶Os/¹⁸⁸Os variations remains uncertain.     

The Isotopic Composition of Noble Gases in Gold Deposits and the Source of Ore- Forming Materials in the Region of North Hebei, China

1IntroductionOnthenorthernmarginoftheNorthChinaplatformislocatedoneofthemostimportantAu Ag polymetallicore concentratedzones,wherethereareavarietyoforetypes .Soithasbeenat tractingeverincreasingattentionofmanygeologists (PeiRongfuetal.,1 998;ShenBaofengetal.,1 994 ;LuSongnianetal.,1 997;HuShouxietal.,1 994 ;ChenYuchuan ,1 999;ZhaiYushengetal.,1 999) .Manyscholarspresentedtheirresearchresultsinvariousaspects.How ever ,thesourceofore formingmaterialshaslongbeenafocusofdiscussion .Studieso…     

Dissolved fluoride in the Lower Ganges-Brahmaputra-Meghna River system in the Bengal Basin, Bangladesh

The dissolved fluoride (F⁻) in the Lower Ganges-Brahmaputra-Meghna (GBM) river system, Bengal basin, Bangladesh, was studied during 1991–1993 to determine its distribution and source in the basin, and its annual flux to the Bay of Bengal. The concentration of dissolved F⁻ varied between 2 and 11 μmol l⁻¹ with statistically significant variations both spatially and temporally in the basin. Such variations are attributable to the geology of the individual subbasins (Ganges, Brahmaputra and Meghna), dilution by rainwater during monsoon and groundwater contribution to the river systems during dry season. Correlation coefficients among F⁻ and major cations and anions suggest diverse inorganic processes responsible for regulating the concentration of F⁻ in these river systems. However, fluorite seems to be one of the major sources of dissolved F⁻. The concentration of F⁻ in the Lower GBM river system is low compared to the rivers draining Deccan Plateau and arid regions of the subcontinent, for example, Yamuna and its tributaries. However, it is within the range of most of the other Peninsular and Himalayan rivers. The GBM system contributes about 115×10³ tonnes year⁻¹ of dissolved F⁻ into the Bay of Bengal, and thus accounts for about 3% of the global F⁻ flux to the oceans annually. Received: 19 May 1999 · Accepted: 11 October 1999     

Helium isotopes in gases of Mineral Waters in the western Caucasus

The He isotope composition as an indicator of mantle-derived component was studied in gases from mineral springs, stratal waters, and mud volcanoes developed west of the Teberda River valley (10 objects) and two springs in the central segment of the Greater Caucasus orogen between the active El’brus and Kazbek volcanoes. In the western segment of the orogen, the values of ³He/⁴He = R_corr vary in the range of (46–114) × 10⁻⁸ = (0.33–0.81)R_atm, where R_atm =1.4 × 10⁻⁶ is the atmospheric ratio. They are substantially lower as compared with values in the vicinity of El’brus and Kazbek and close to those in samples from the central segment equal to (70–134) × 10⁻⁸ = (0.50–0.96)R_atm, as well as to the values previously recorded in the Caucasian Mineral Waters (CMW) area. Moreover, the content of ³He in them is notably higher as compared with its crustal radiogenic level characteristic of mud volcanoes in the Taman Peninsula, where R = (1.4–2.8) × 10⁻⁸ = (0.01–0.02)R_atm. Nitrogen-methane gas from northern piedmonts of the western Caucasus also contain nonatmogenic components, including the radiogenic ⁴⁰Ar (⁴⁰Ar/³⁶Ar = 900), “excess” nitrogen (∼87% of the total N₂ concentration in sample) and the mantle He. These data specify the distribution of mantle derivates along the orogen strike and age of intrusive magmatic activity in its different segments.     

Hydraulic properties of the crystalline basement

Hydraulic tests in boreholes, up to 4.5 km deep, drilled into continental crystalline basement revealed hydraulic conductivity (K) values that range over nine log-units from 10⁻¹³−10⁻⁴ m s⁻¹. However, K values for fractured basement to about 1 km depth are typically restricted to the range from 10⁻⁸ to 10⁻⁶ m s⁻¹. New data from an extended injection test at the KTB research site (part of the Continental Deep Drilling Program in Germany) at 4 km depth provide K=5 10⁻⁸ m s⁻¹. The summarized K-data show a very strong dependence on lithology and on the local deformation history of a particular area. In highly fractured regions, granite tends to be more pervious than gneiss. The fracture porosity is generally saturated with Na–Cl or Ca–Na–Cl type waters with salinities ranging from <1 to >100 g L⁻¹. The basement permeability is well within the conditions for advective fluid and heat transport. Consequently, fluid pressure is hydrostatic and a Darcy flow mechanism is possible to a great depth. Topography-related hydraulic gradients in moderately conductive basement may result in characteristic advective flow rates of up to 100 L a⁻¹ m⁻² and lead to significant advective heat and solute transfer in the upper brittle crust. An erratum to this article can be found at     

The impact of over 100 years of wildfires on mercury levels and accumulation rates in two lakes in southern California,USA

In southern California, USA, wildfires may be an important source of mercury (Hg) to local watersheds. Hg levels and Hg accumulation rates were investigated in dated sediment cores from two southern California lakes, Big Bear Lake and Crystal Lake, located approximately 40-km apart. Between 1895 and 2006, fires were routinely minimized or suppressed around Big Bear Lake, while fires regularly subsumed the forest surrounding Crystal Lake. Mean Hg concentrations and mean Hg accumulation rates were significantly higher in Crystal Lake sediments compared to Big Bear Lake sediments (Hg levels: Crystal Lake 220 ± 93 ng g⁻¹, Big Bear Lake 92 ± 26 ng g⁻¹; Hg accumulation: Crystal Lake 790 ± 1,200 μg m⁻² year⁻¹, Big Bear 240 ± 54 μg m⁻² year⁻¹). In Crystal Lake, the ratio between post-1965 and pre-1865 Hg concentrations was 1.1, and several spikes in Hg levels occurred between 1910 and 1985. Given the remote location of the lake, the proximity of fires, and the lack of point sources within the region, these results suggested wildfires (rather than industrial sources) were a continuous source of Hg to Crystal Lake over the last 150 years.     

Inorganic nitrogen dynamics in intertidal rocky biofilms and sediments of the Douro River estuary (Portugal)

In this study rates of oxygen, ammonium (NH₄ ⁺), nitrate (NO₃ ⁻), nitrite (NO₂ ⁻), and nitrous oxide (N₂O) fluxes, nitrogen (N) fixation, nitrification, and denitrification were compared between two intertidal sites for which there is an abundant global literature, muddy and sandy sediments, and two sites representing the rocky intertidal zone where biogeochemical processes have scarcely been investigated. In almost all sites oxygen production rates greatly exceeded oxygen consumption rates. During daylight, NH₄ ⁺ and NO₃ ⁻ uptake rates together with ammonification could supply the different N requirements of the primary producer communities at all four sites; N assimilation by benthic or epilithic primary producers was the major process of dissolved inorganic nitrogen (DIN) removal; N fixation, nitrification, and denitrification were minor processes in the overall light DIN cycle. At night, distinct DIN cycling processes took place in the four environments, denitrification rates ranged from 9 ± 2 to 360 ± 30 μmol N₂ m⁻² h⁻¹, accounting for 10–48% of the water column NO₃ ⁻ uptake; nitrification rates varied from 0 to 1712 ± 666 μmol NH₄ ⁺ m⁻² h⁻¹. A conceptual model of N cycle dynamics showed major differences between intertidal sediment and rocky sites in terms of the mean rates of DIN net fluxes and the processes involved, with rocky biofilm showing generally higher fluxes. Of particular significance, the intertidal rocky biofilms released 10 times the amount of N₂O produced in intertidal sediments (up to 17 ± 6 μmol N₂O m⁻² h⁻¹), representing the highest N₂O release rates ever recorded for marine systems. The biogeochemical contributions of intertidal rocky substrata to estuarine and coastal processes warrant future detailed investigation.     

Geochemistry characterization of groundwater in an agricultural area of Razan,Hamadan, Iran

This study was conducted to evaluate factors regulating groundwater quality in an area with agriculture as main use. Thirty groundwater samples have been collected from Razan area (Hamadan, Iran) for hydrochemical investigations to understand the sources of dissolved ions and assess the chemical quality of the groundwater. The chemical compositions of the groundwater are dominated by Na⁺, Ca²⁺, HCO₃ ⁻, Cl⁻ and SO₄ ²⁻, which have been derived largely from natural chemical weathering of carbonate, gypsum and anthropogenic activities of fertilizer’s source. The production of SO₄ ²⁻ has multiple origins, mainly from dissolution of sulphate minerals, oxidation of sulphide minerals and anthropogenic sources. The major anthropogenic components in the groundwater include Na⁺, Cl⁻, SO₄ ²⁻ and NO₃ ⁻, with Cl⁻ and NO₃ ⁻ being the main contributors to groundwater pollution in Razan area.     

Rare-earth elements as source indicators of Pan-African granites from Obudu Plateau,Southeastern Nigeria

The rare-earth element （REE） concentrations of representative granite samples from the southeast of the Obudu Plateau, Nigeria, were analyzed with an attempt to determine the signatures of their source, evolutionary history and tectonic setting. Results indicated that the granites have high absolute REE concentrations （190×10^-6-1191×10^-6; av.=549×10^-6） with the chondrite-normalized REE patterns characterized by steep negative slopes and prominent to slight or no negative Eu anomalies. All the samples are also characterized by high and variable concentrations of the LREE （151×10^-6-1169×10^-6; av.= 466×10^-6）, while the HREE show low abundance （4×10^-6-107×10^-6; av.=28×10^-6）. These are consistent with the variable levels of REE fractionation, and differentiation of the granites. This is further supported by the range of REE contents, the chondrite-normalized patterns and the ratios of LaN/YbN （2.30-343.37）, CeN/YbN （5.94-716.87）, LaN/SmN （3.14-11.68） and TbN/YbN （0.58-1.65）. The general parallelism of the REE patterns, suggest that all the granites were comagmatic in origin, while the high Eu/Eu＊ ratios （0.085-2.807; av.=0.9398） indicate high fo2 at the source. Similarly, irregular variations in LaN/YbN, CeN/YbN and Eu/Eu＊ ratios and REE abundances among the samples suggest behaviors that are related to mantle and crustal sources.     

Constraints on the Source Components of Lavas Forming the Hawaiian North Arch and Honolulu Volcanics

Hawaiian volcanoes, dominantly shields of tholeiitic basalt,form as the Pacific Plate migrates over a hotspot in the mantle.As these shields migrate away from the hotspot, highly alkaliclavas, forming the rejuvenated stage of volcanism, may eruptafter an interval of erosion lasting for 0·25–2·5Myr. Alkalic lavas with geochemical characteristics similarto rejuvenated- stage lavas erupted on the sea floor north ofOahu along the Hawaiian Arch. The variable Tb/Yb, Sr/Ce, K/Ce,Rb/La, Ba/La, Ti/Eu and Zr/Sm ratios in lavas forming the NorthArch and the rejuvenated-stage Honolulu Volcanics were controlledduring partial melting by residual garnet, clinopyroxene, Fe–Tioxides and phlogopite. However, the distinctively high Ba/Thand Sr/Nd ratios of lava forming the North Arch and HonoluluVolcanics reflect source characteristics. These characteristicsare also associated with shield tholeiitic basalt; hence theyarise from the Hawaiian hotspot, which is interpreted to bea mantle plume. Inversion of the batch melting equation usingabundances of highly incompatible elements, such as Th and La,requires enriched sources with 10–55% clinopyroxene and5–25% garnet for North Arch lavas. The ⁸⁷Sr/⁸⁶Sr and ¹⁴³Nd/¹⁴⁴Ndratios in lavas forming the North Arch and Honolulu Volcanicsare consistent with mixing between the Hawaiian plume and adepleted component related to mid-ocean ridge basalts. Specifically,the enrichment of incompatible elements coupled with low ⁸⁷Sr/⁸⁶Srand high ¹⁴³Nd/¹⁴⁴Nd relative to bulk Earth ratios is best explainedby derivation from depleted lithosphere recently metasomatizedby incipient melt (<2% melting) from the Hawaiian plume.In this metasomatized source, the incompatible element abundances,as well as Sr and Nd isotopic ratios, are controlled by incipientmelts. In contrast, the large range of published ¹⁸⁷Os/¹⁸⁸Osdata (0·134–0·176) reflects heterogeneitycaused by various proportions of pyroxenite veins residing ina depleted peridotite matrix. KEY WORDS: Hawaiian plume; Honolulu Volcanics; North Arch; plume–lithosphere interaction; rejuvenated stage; trace element geochemistry; alkalic lavas     

Saturated permeability measurements on pumice and welded-tuffaceous materials

Fluid flows in consolidated porous media of volcanic origin are being investigated to support such diverse efforts as the modeling of thermal/outgassing phenomena at Mount St. Helens and the hydrological modeling of tuffaceous rocks in support of the Department of Energy’s (DOE) Nevada Nuclear Waste Storage Investigations Project An experimental apparatus was designed and built to allow water-saturated permeabilities as low as 10⁻¹⁸ m² to be measured on cores of diameter 5 cm and length 10 cm under steady-state flow conditions. This same apparatus can also be utilized in a transient (pressure-decay) mode in order to measure permeabilities several orders of magnitude lower than the steady-state limit. Tests were conducted on samples of pumice, fractured welded tuff, and welded tuff, representing a permeability range of seven orders of magnitude Pumice was found to have a permeability of ∼3×10⁻¹² m², sufficiently high to allow the complete Darcy-to-Ergun regime to be investigated Welded (unfractured) tuff was tested in the transient mode, yielding a permeability of ∼5×10⁻¹⁹ m². Two, long-time-scale, steady-flow experiments were conducted on a core of welded tuff containing a single, through-going fracture. For the first experiment, the core was an integral cylinder containing a naturally occurring fracture. For the second experiment, the core was separated into two pieces along the existing fracture plane, then rejoined. Effects of essentially constant, as well as rapidly varied, circumferential stress were studied in both tests. Results showed core permeability to decay to 2×10⁻¹⁸ m² in both cases, independent of the initial fracture state (closed versus open). With a naturally occurring fracture, core permeability decreased by a factor of 2 over a 200-h test period. With an initially open fracture, core permeability decreased by a factor of 4 under the influence of a comparable 200-h load-time history, after 700 h of testing, core permeability was reduced by an order of magnitude from its initial level. Final effective hydraulic fracture aperture was calculated to be 10⁻⁶ m, corresponding to a calculated effective fracture permeability of 10⁻¹³ m² Fracture flow was thus estimated to account for 80% of the total flow rate through this core under final test conditions.     

Atmospheric aerosol formation and its growth during the cold season in India

The effects of molecular diffusivity of H₂SO₄ and NH₃ vapours on nucleated particles of SO₄²⁻ and NO₃⁻ species are reported. Condensation sink and source rate of H₂SO₄ and NH₃ vapours, growth rates and ratios of real to apparent nucleation rates are calculated for SO₄^– and NO₃⁻ aerosols using fractional contributions of them in total aerosol size-distribution during the measurement period at Pune, reported in Chate and Pranesha (2004). The percentage of nucleated SO₄²⁻ and NO₃⁻ aerosols of mid-point diameter 13 nm are 2% and 3% respectively of the total particles (13 nm ≤ D _p ≤ 750 nm) for both H₂SO₄ and NH₃ diffusion. In the diameter range 75 nm ≤ D _p ≤ 133 nm, it is 48% and 45% of SO₄²⁻ and NO₃⁻ aerosols, respectively for NH₃ diffusion and 43% and 36% of SO₄²⁻ and NO₃⁻ for H₂SO₄ diffusion. Increase in percentage of nucleated particles of these species corresponding to mid-point diameter 133 nm around 0900 h IST is significantly higher than that of mid-point diameter 13 nm and it is due to photo-chemical nucleation, coagulation and coalescence among nucleated clusters. The ratios of real to apparent formation rates for SO₄²⁻ and NO₃⁻ aerosols are 12% and 11% respectively, corresponding to mid-point diameter 13 nm, 17% and 13%, for midpoint diameter 133 nm and 12% and 9.5%, for mid-point diameter 750 nm. The results indicate that nucleation involving H₂SO₄ and acidic NH₃ diffusion on SO₄²⁻ and NO₃⁻ particles is the most relevant mechanism in this region.     

Estimation of methane emission from whole waste landfill site using correlation between flux and ground temperature

A methodology to estimate a methane emission in a waste landfill site was developed. The methane flux at a waste landfill site in summer, autumn, and winter was within the following ranges: from −1.3×10⁻² to 16, from −6.4×10⁻² to 7.5, and from −1.6×10⁻³ to 1.5×10⁻² g-CH₄ m⁻² h⁻¹, respectively. In those seasons, the mean methane emission rate and coefficient of variation were 1.1 g-CH₄ m⁻² h⁻¹ ±290%, 0.57 g-CH₄ m⁻² h⁻¹ ±347%, and 5.4×10⁻² g-CH₄ m⁻² h⁻¹ ±370%, respectively. These results simultaneously showed that fluctuations of methane emission from the landfill surface were both of spatial and temporal variability. In each season, an exponential relationship was observed between the methane flux density and the ground temperature. Total methane emissions were estimated to be 5.7×10⁻², 7.1×10⁻³, and 1.7×10⁻³ g-CH₄ m⁻² h⁻¹ in the summer, autumn, and winter surveys, respectively, using a temperature surrogated-kriging method. The results of this study would improve upon the labor-intensive closed-chamber method, and could be a more practical way to estimate methane emissions from waste landfills.     

Temporal variability in summertime bottom hypoxia in shallow areas of Mobile Bay,Alabama

This paper addresses temporal variability in bottom hypoxia in broad shallow areas of Mobile Bay, Alabama. Time-series data collected in the summer of 2004 from one station (mean depth of 4 m) exhibit bottom dissolved oxygen (DO) variations associated with various time scales of hours to days. Despite a large velocity shear, stratification was strong enough to suppress vertical mixing most of the time. Bottom DO was closely related to the vertical salinity gradient (ΔS). Hypoxia seldom occurred when ΔS (over 2.5 m) was <2 psu and occurred almost all the time when ΔS was >8 psu in the absence of extreme events like hurricanes. Oxygen balance between vertical mixing and total oxygen demand was considered for bottom water from which oxygen demand and diffusive oxygen flux were estimated. The estimated decay rates at 20°C ranging between 0.175–0.322 d⁻¹ and the corresponding oxygen consumption as large as 7.4 g O₂ m⁻² d⁻¹ fall at the upper limit of previously reported ranges. The diffusive oxygen flux and the corresponding vertical diffusivity estimated for well mixed conditions range between 8.6–9.5 g O₂ m⁻² d⁻¹ and 2.6–2.9 m² d⁻¹, respectively. Mobile Bay hypoxia is likely to be associated with a large oxygen demand, supported by both water column and sediment oxygen demands, so that oxygen supply from surface water during destratification events would be quickly exhausted to return to hypoxic conditions within a few hours to days after destratification events are terminated.     

Diffusion of tetravalent cations in zircon

Diffusion rates for the three tetravalent cations U, Th and Hf have been measured in synthetic zircon. Diffusant sources included oxide powders and ground pre-synthesized silicates. Rutherford backscattering spectrometry (RBS) was used to measure depth profiles. Over the temperature range 1400–1650 °C, the following Arrhenius relations were obtained (diffusion coefficients in m²sec⁻¹): log D _Th = (1.936 ± 0.9820) + (− 792 ± 34 kJ mol⁻¹ /2.303 RT) log D _U = (0.212 ± 2.440) + (− 726 ± 83 kJ mol⁻¹ /2.303 RT) log D _Hf = (3.206 ± 1.592) + (− 812 ± 54 kJ mol⁻¹ /2.303 RT) The data show a systematic increase in diffusivity with decreasing ionic radius (i.e., faster diffusion rates for Hf than for U or Th), a trend also observed in our earlier study of rare earth diffusion in zircon. Diffusive fractionation may be a factor in the Lu-Hf system given the much slower diffusion rates of tetravalent cations when compared with the trivalent rare earths. The very slow diffusion rates measured for these tetravalent cations suggest that they are essentially immobile under most geologic conditions, permitting the preservation of fine-scale chemical zoning and isotopic signatures of inherited cores. Received: 12 July 1996 / Accepted: 2 December 1996     

Geochemistry and environmental effect of cadmium in the super-large Jinding Pb-Zn deposit,Yunnan Province,China

The Jinding Pb-Zn deposit in Yunnan Province is the representative of a Cd-enriched area and mining activities lead to the release of Cd into the hypergenic ecosystem, resulting in Cd pollution. The concentrations of Cd vary greatly from one type to another type of rocks in the mining district. In the host rock, Cd concentrations range from 50×10^-6 to 650×10^-6 with an average of 310×10^-6. In primary ores, Cd concentrations range from 14×10^-6 to 2800×10^-6 with an average of 767×10^-6. However, in oxidized ores, Cd concentrations are highest, varying within the range of 110×10^-6 to 8200×10^-6 , averaging 1661×10^-6. It is shown that the oxidized ores are the main carder and environmental source of Cd. Leaching test showed that Pb/Zn ores are easy to oxidize and thereafter release Cd and other harmful elements. These leached elements in the leachate may be precipitated rapidly in the order of Zn〉Pb〉Cd. As for the concentration distribution of Cd in the Bijiang River, it is estimated to be 15.7 μg/L Cd in water, 49.3 mg/L in suspended substances, and 203.7 mg/L in sediments. The average value of Cd in soil from the polluted area is 83.0 mg/kg. Natural weathering of Cd-rich rocks and minerals imposes a potential environmental risk on the aquatic ecosystem of the Bijiang catchment.     

Reactions and reaction rates in the regional aquifer beneath the Pajarito Plateau,north-central New Mexico,USA

Reactions and reaction rates within aquifers are fundamental components of critical hydrological processes. However, reactions simulated in laboratory experiments typically demonstrate rates that are much faster than those observed in the field. Therefore, it is necessary to conduct more reaction rate analyses in natural settings. This study of geochemical reactions in the regional aquifer in the Pajarito Plateau near Los Alamos, New Mexico combines modeling with petrographic assessment to further knowledge and understanding of complex natural hydrologic systems. Groundwater geochemistry shows marked evolution along assumed flow paths. The flow path chosen for this study was evaluated using inverse mass balance modeling to calculate the mass transfer. X-ray diffraction and field emission gun scanning electron microscopy were used to identify possible reactants and products. Considering the mineralogy of the aquifer and saturation indices for the regional water refined initial interpretations. Calculations yielded dissolution rates for plagioclase on the order of 10⁻¹⁵ mol s⁻¹ m⁻² and for K-feldspar on the order of 10⁻¹⁷ mol s⁻¹ m⁻², orders of magnitude slower than laboratory rates. While these rates agree with other aquifer studies, they must be considered in the light of the uncertainty associated with geometric surface area estimates, ¹⁴C ages, and aquifer properties.     

Heterogeneous mantle source and magma differentiation of quaternary arc-like volcanic rocks from Tengchong,SE margin of the Tibetan Plateau

The Tengchong volcanic field north of the Burma arc comprises numerous Quaternary volcanoes in the southeastern margin of the Tibetan Plateau. The volcanic rocks are grouped into four units (1–4) from the oldest to youngest. Units 1, 3 and 4 are composed of olivine trachybasalt, basaltic trachyandesite and trachyandesite, and Unit 2 consists of hornblende dacite. The rocks of Units 1, 3, and 4 form a generally alkaline suite in which the rocks plot along generally linear trends on Harker diagrams with only slight offset from unit to unit. They contain olivine phenocrysts with Fo values ranging from 65 to 85 mol% and have Cr-spinel with Cr# ranging from 23 to 35. All the rocks have chondrite-normalized REE patterns enriched in LREE and primitive mantle-normalized trace element patterns depleted in Ti, Nb and Ta, but they are rich in Th, Ti and P relative to typical arc volcanics. Despite minor crustal contamination, ⁸⁷Sr/⁸⁶Sr ratios (0.706–0.709), εNd values (−3.2 to −8.7), and εHf values (+4.8 to −6.4) indicate a highly heterogeneous mantle source. The Pb isotopic ratios of the lavas (²⁰⁶Pb/²⁰⁴Pb = 18.02–18.30) clearly show an EMI-type mantle source. The underlying mantle source was previously modified by subduction of the Neo-Tethyan oceanic and Indian continental lithosphere. The present heterogeneous mantle source is interpreted to have formed by variable additions of fluids and sediments derived from the subducted Indian Oceanic lithosphere, probably the Ninety East Ridge. Magma generation and emplacement was facilitated by transtensional NS-trending strike-slip faulting.