Spectral Irradiance, Phytoplankton Community Composition and Primary Productivity in a Salt Marsh Estuary, North Inlet, South Carolina, USA

We investigated spatial and temporal changes in spectral irradiance, phytoplankton community composition, and primary productivity in North Inlet Estuary, South Carolina, USA. High concentrations of colored dissolved organic matter (CDOM) were responsible for up to 84 % of the attenuation of photosynthetically available radiation (PAR). Green-yellow wavelengths were the predominant colors of light available at the two sampling sites: Clam Bank Creek and Oyster Landing. Vertical attenuation coefficients of PAR were 0.7–2.1 m^?1 with corresponding euphotic zone depths of 1.5–6.7 m. Phytoplankton biomass (as chlorophyll a [chl a]) varied seasonally with a summer maximum of 16 μg chl a l^?1 and a winter minimum of 1.4 μg chl a l^?1. The phytoplankton community consisted mainly of diatoms, prasinophytes, cryptophytes and haptophytes, with diatoms and prasinophytes accounting for up to 67 % of total chl a. Changes in phytoplankton community composition showed strongest correlations with temperature. Light-saturated chl a-specific rates of photosynthesis and daily primary productivity varied with season and ranged from 1.6 to 14 mg C (mg chl a) ^?1?h^?1 (32–803 mg C m^?3?day^?1). Calculated daily rates added up to an annual carbon fixation rate of 84 g C m^?3?year^?1. Overall, changes in phytoplankton community composition and primary productivity in North Inlet showed a strong dependence on temperature, with PAR and spectral irradiance playing a relatively minor role due to short residence times, strong tidal forcing and vertical mixing.     

Carbon Dioxide Fluxes and Their Environmental Control in a Reclaimed Coastal Wetland in the Yangtze Estuary

Large areas of natural coastal wetlands have suffered severely from human-driven damages or conversions (e.g., land reclamations), but coastal carbon flux responses in reclaimed wetlands are largely unknown. The lack of knowledge of the environmental control mechanisms of carbon fluxes also limits the carbon budget management of reclaimed wetlands. The net ecosystem exchange (NEE) in a coastal wetland at Dongtan of Chongming Island in the Yangtze estuary was monitored throughout 2012 using the eddy covariance technique more than 14 years after this wetland was reclaimed using dykes to stop tidal flooding. The driving biophysical variables of NEE were also examined. The results showed that NEE displayed marked diurnal and seasonal variations. The monthly mean NEE showed that this ecosystem functioned as a CO₂ sink during 9 months of the year, with a maximum value in September (?101.2 g C m^?2) and a minimum value in November (?8.2 g C m^?2). The annual CO₂ balance of the reclaimed coastal wetland was ?558.4 g C m^?2 year^?1. The ratio of ecosystem respiration (ER) to gross primary production (GPP) was 0.57, which suggests that 57 % of the organic carbon assimilated by wetland plants was consumed by plant respiration and soil heterotrophic respiration. Stepwise multiple linear regressions suggested that temperature and photosynthetically active radiation (PAR) were the two dominant micrometeorological variables driving seasonal variations in NEE, while soil moisture (M _s) and soil salinity (PS_s) played minor roles. For the entire year, PAR and daytime NEE were significantly correlated, as well as temperature and nighttime NEE. These nonlinear relationships varied seasonally: the maximum ecosystem photosynthetic rate (A _max), apparent quantum yield (?), and Q ₁₀ reached their peak values during summer (17.09 μmol CO₂?m^?2 s^?1), autumn (0.13 μmol CO₂?μmol^?1 photon), and spring (2.16), respectively. Exceptionally high M _s or PS_s values indirectly restricted ecosystem CO₂ fixation capacity by reducing the PAR sensitivity of the NEE. The leaf area index (LAI) and live aboveground biomass (AGB_L) were significantly correlated with NEE during the growing season. Although the annual net CO₂ fixation rate of the coastal reclaimed wetland was distinctly lower than the unreclaimed coastal wetland in the same region, it was quite high relative to many inland freshwater wetlands and estuarine/coastal wetlands located at latitudes higher than this site. Thus, it is concluded that although the net CO₂ fixation capacity of the coastal wetland was reduced by land reclamation, it can still perform as an important CO₂ sink.     

The removal kinetics of dissolved organic matter and the optical clarity of groundwater

Concentrations of dissolved organic matter (DOM) and ultraviolet/visible light absorbance decrease systematically as groundwater moves through the unsaturated zones overlying aquifers and along flowpaths within aquifers. These changes occur over distances of tens of meters (m) implying rapid removal kinetics of the chromophoric DOM that imparts color to groundwater. A one-compartment input-output model was used to derive a differential equation describing the removal of DOM from the dissolved phase due to the combined effects of biodegradation and sorption. The general solution to the equation was parameterized using a 2-year record of dissolved organic carbon (DOC) concentration changes in groundwater at a long-term observation well. Estimated rates of DOC loss were rapid and ranged from 0.093 to 0.21 micromoles per liter per day (μM d^?1), and rate constants for DOC removal ranged from 0.0021 to 0.011 per day (d^?1). Applying these removal rate constants to an advective-dispersion model illustrates substantial depletion of DOC over flow-path distances of 200 m or less and in timeframes of 2 years or less. These results explain the low to moderate DOC concentrations (20–75 μM; 0.26–1 mg L^?1) and ultraviolet absorption coefficient values (a ₂₅₄?<?5 m^?1) observed in groundwater produced from 59 wells tapping eight different aquifer systems of the United States. The nearly uniform optical clarity of groundwater, therefore, results from similarly rapid DOM-removal kinetics exhibited by geologically and hydrologically dissimilar aquifers.     

Carbon dioxide fluxes over a temperate meadow in eastern Inner Mongolia,China

Understanding the carbon dynamics in grassland is essential to precisely estimate global atmospheric carbon budget in response to climatic change. Eddy flux measurements were carried out during 2011 and 2012 to characterize seasonal and annual variability of carbon exchanges above a temperate meadow in eastern Inner Mongolia, China. The CO₂ flux showed obvious diurnal variations and the monthly mean amplitudes of diurnal course followed June/July > August > May > September. The daily maximum NEE reached up to ?8.0 and ?7.7 g C m^?2 for 2011 and 2012, respectively. CO₂ uptake was mainly from May to August, with seasonal peaks of ?16.0 g C m^?2 day^?1 in both two years. Gross primary production (GPP) and ecosystem respiration (Re) were ?1,084.5, 987.1 g C m^?2 year^?1 in 2011, and ?1,123.3, 1,040.2 g C m^?2 year^?1 in 2012, respectively. The meadow acted as a stable carbon sink, with integrated net ecosystem exchange (NEE) of ?97.4 and ?83.1 g C m^?2 year^?1 for 2011 and 2012, respectively. Compared with 2011, the ecosystem assimilated more carbon and meanwhile respired even more, leading to a less carbon sequestration in 2012. PAR and leaf area index (LAI) dominated the seasonal variations in NEE, with PAR explaining 61–69 % of the variance in NEE as LAI maintaining the plateau during June to July. Harvest significantly decreased ecosystem carbon uptake. The interannual variability in GPP and Re resulted primarily from the variations in temperature and its effect on biomass growth.     

Anaerobic Carbon Mineralisation Through Sulphate Reduction in the Inner Shelf Sediments of Eastern Arabian Sea

Monsoon-induced coastal upwelling, land run-off, benthic and atmospheric inputs make the western Indian shelf waters biologically productive that is expected to lead to high rates of mineralisation of organic matter (OM) in the sediments. Dissimilatory sulphate reduction (SR) is a major pathway of OM mineralisation in near-shore marine sediments owing to depletion of other energetically more profitable electron acceptors (O₂, NO₃ ^?, Mn and Fe oxides) within few millimetres of the sediment-water interface. We carried out first ever study to quantify SR rates in the inner shelf sediments off Goa (central west coast of India) using the ³⁵S radiotracer technique. The highest rates were recorded in the upper 10 cm of the sediment cores and decreased gradually thereafter below detection. Despite significant SR activity in the upper ～12 to 21 cm at most of the sites, pore water sulphate concentrations generally did not show much variation with depth. The depth integrated SR rate (0.066–0.46 mol m^?2 year^?1) decreased with increasing water depth. Free sulphide was present in low concentrations (0–3 μM) in pore waters at shallow stations (depth <30 m). However, high build-up of sulphide (100–600 μM) in pore waters was observed at two deeper stations (depths 39 and 48 m), 7–11 cm below the sediment-water interface. The total iron content of the sediment decreased from ～7 to 5 % from the shallowest to the deepest station. The high pyrite content indicates that the shelf sediments act as a sink for sulphide accounting for the low free sulphide levels in pore water. In the moderately organic rich (2–3.5 %) sediments off Goa, the measured SR rates are much lower than those reported from other upwelling areas, especially off Namibia and Peru. The amount of organic carbon remineralised via sulphate reduction was ～0.52 mol m^?2 year^?1. With an estimated average organic carbon accumulation rate of ～5.6 (±0.5) mol m^?2 year^?1, it appears that the bulk of organic matter gets preserved in sediments in the study region.     

The Impact of Sediment and Carbon Fluxes on the Biogeochemistry of Methane and Sulfur in Littoral Baltic Sea Sediments (Himmerfjärden, Sweden)

Three sediment stations in Himmerfjärden estuary (Baltic Sea, Sweden) were sampled in May 2009 and June 2010 to test how low salinity (5–7 ‰), high primary productivity partially induced by nutrient input from an upstream waste water treatment plant, and high overall sedimentation rates impact the sedimentary cycling of methane and sulfur. Rates of sediment accumulation determined using ²¹⁰Pb_excess and ¹³⁷Cs were very high (0.65–0.95 cm?year^?1), as were the corresponding rates of organic matter accumulation (8.9–9.5 mol C?m^?2?year^?1) at all three sites. Dissolved sulfate penetrated <20 cm below the sediment surface. Although measured rates of bicarbonate methanogenesis integrated over 1 m depth were low (0.96–1.09 mol?m^?2?year^?1), methane concentrations increased to >2 mmol?L^?1 below the sulfate–methane transition. A steep gradient of methane through the entire sulfate zone led to upward (diffusive and bio-irrigative) fluxes of 0.32 to 0.78 mol?m^?2?year^?1 methane to the sediment–water interface. Areal rates of sulfate reduction (1.46–1.92 mol?m^?2?year^?1) integrated over the upper 0–14 cm of sediment appeared to be limited by the restricted diffusive supply of sulfate, low bio-irrigation (α?=?2.8–3.1 year^?1), and limited residence time of the sedimentary organic carbon in the sulfate zone. A large fraction of reduced sulfur as pyrite and organic-bound sulfur was buried and thus escaped reoxidation in the surface sediment. The presence of ferrous iron in the pore water (with concentrations up to 110 μM) suggests that iron reduction plays an important role in surface sediments, as well as in sediment layers deep below the sulfate–methane transition. We conclude that high rates of sediment accumulation and shallow sulfate penetration are the master variables for biogeochemistry of methane and sulfur cycling; in particular, they may significantly allow for release of methane into the water column in the Himmerfjärden estuary.     

Geological and isotopic evidence for magmatic-hydrothermal origin of the Ag–Pb–Zn deposits in the Lengshuikeng District,east-central China

The Lengshuikeng ore district in east-central China has an ore reserve of ～43 Mt with an average grade of 204.53 g/t Ag and 4.63 % Pb?+?Zn. Based on contrasting geological characteristics, the mineralization in the Lengshuikeng ore district can be divided into porphyry-hosted and stratabound types. The porphyry-hosted mineralization is distributed in and around the Lengshuikeng granite porphyry and shows a distinct alteration zoning including minor chloritization and sericitization in the proximal zone; sericitization, silicification, and carbonatization in the peripheral zone; and sericitization and carbonatization in the distal zone. The stratabound mineralization occurs in volcano-sedimentary rocks at ～100–400 m depth without obvious zoning of alterations and ore minerals. Porphyry-hosted and stratabound mineralization are both characterized by early-stage pyrite–chalcopyrite–sphalerite, middle-stage acanthite–native silver–galena–sphalerite, and late-stage pyrite–quartz–calcite. The δ³⁴S values of pyrite, sphalerite, and galena in the ores range from ?3.8 to +6.9‰ with an average of +2.0‰. The C–O isotope values of siderite, calcite, and dolomite range from ?7.2 to ?1.5‰ with an average of ?4.4‰ (V-PDB) and from +10.9 to +19.5‰ with an average of +14.8‰ (V-SMOW), respectively. Hydrogen, oxygen, and carbon isotopes indicate that the hydrothermal fluids were derived mainly from meteoric water, with addition of minor amounts of magmatic water. Geochronology employing LA–ICP–MS analyses of zircons from a quartz syenite porphyry yielded a weighted mean ²⁰⁶Pb/²³⁸U age of 136.3?±?0.8 Ma considered as the emplacement age of the porphyry. Rb–Sr dating of sphalerite from the main ore stage yielded an age of 126.9?±?7.1 Ma, marking the time of mineralization. The Lengshuikeng mineralization classifies as an epithermal Ag–Pb–Zn deposit.     

Genesis of wollastonite- and grandite-rich skarns in a suite of marble-calc-silicate rocks from Sittampundi, Tamil Nadu: constraints on the P–T–fluid regime in parts of the Pan-African mobile belt of South India

The Pan-African tectonothermal activities in areas near Sittampundi, south India, are characterized by metamorphic changes in an interlayered sequence of migmatitic metapelites, marble and calc-silicate rocks. This rock sequence underwent multiple episodes of folding, and was intruded by granite batholiths during and subsequent to these folding events. The marble and the calc-silicate rocks develop a variety of skarns, which on the basis of mineralogy; can be divided into the following types: Type I: wollastonite?+?clinopyroxene (mg#?=?71–73)?+?grandite (16–21 mol% Adr)?+?quartz?±?calcite, Type II: grandite (25–29 mol% Adr )?+?clinopyroxene (mg#?=?70)?+?calcite?+?quartz, and Type III: grandite (36–38 mol% Adr)?+?clinopyroxene (mg#?=?55–65)?+?epidote?+?scapolite?+?calcite?+?quartz. Type I skarn is 2–10 cm thick, and is dominated by wollastonite (>70 vol%) and commonly occurs as boudinaged layers parallel to the regional foliation Sn₁ related to the Fn₁ folds. Locally, thin discontinuous lenses and stringers of this skarn develop along the axial planes of Fn₂ folds. The Type II skarn, on the other hand, is devoid of wollastonite, rich in grandite garnet (40–70 vol%) and developed preferentially at the interface of clinopyroxene-rich calc-silicates layers and host marble during the later folding event. Reaction textures and the phase compositional data suggest the following reactions in the skarns: 1. calcite?+?SiO₂?→?wollastonite?+?V, 2. calcite?+?clinopyroxene?+?O₂?→?grandite?+?SiO₂?+?V, 3. scapolite?+?calcite?+?quartz?+?clinopyroxene?+?O₂?→?grandite?+?V and 4. epidote?+?calcite?+?quartz?+?clinopyroxene?+?O₂?→?grandite?+?V Textural relations and composition of phases demonstrate that (a) silica metasomatism of the host marble by infiltration of aqueous fluids (X_CO2?<?0.15) led to production of large volumes of wollastonite in the wollastonite-rich skarn whereas mobility of FeO, SiO₂ and CaO across the interface of marble and calc-silicate and infiltration of aqueous fluids (X_CO2?<?0.35) were instrumental for the formation of grandite skarns. Composition of minerals in type II skarn indicates that Al₂O₃ was introduced in the host marble by the infiltrating fluid. Interpretation of mineral assemblages observed in the interlayered metapelites and the calcareous rocks in pseudosections, isothermal P-X_CO2 and isobaric T-X_CO2 diagrams tightly bracket the “peak” metamorphic conditions at c.9?±?1 kbar and 750°?±?30°C. Subsequent to ‘peak’ metamorphic conditions, the rocks were exhumed on a steeply decompressive P–T path. The estimated ‘peak’ P–T estimates are inconsistent with the “extreme” metamorphic conditions (>11 kbar and >950°C) inferred for the Pan-African tectonothermal events from the neighboring areas. Field and petrological attributes of these skarn rocks are consistent with the infiltration of aqueous fluid predominantly during the Fn₁ folding event at or close to the ‘peak’ metamorphic conditions. Petrological features indicate that the buffering capacity of the rocks was lost during the formation of type I and II skarns. However, the host rock could buffer the composition of the permeated fluids during the formation of type III skarn. Aqueous fluids derived from prograde metamorphism of the metapelites seem to be the likely source for the metasomatic fluids that led to the formation of the skarn rocks.     

Nanoscale zero-valent iron flakes for groundwater treatment

Even today the remediation of organic contaminant source zones poses significant technical and economic challenges. Nanoscale zero-valent iron (NZVI) injections have proved to be a promising approach especially for source zone treatment. We present the development and the characterization of a new kind of NZVI with several advantages on the basis of laboratory experiments, model simulations and a field test. The developed NZVI particles are manufactured by milling, consist of 85 % Fe(0) and exhibit a flake-like shape with a thickness of <100 nm. The mass normalized perchloroethylene (PCE) dechlorination rate constant was 4.1 × 10^?3 L/g h compared to 4.0 × 10^?4 L/g h for a commercially available reference product. A transport distance of at least 190 cm in quartz sand with a grain size of 0.2–0.8 mm and Fe(0) concentrations between 6 and 160 g/kg (sand) were achieved without significant indications of clogging. The particles showed only a low acute toxicity and had no longterm inhibitory effects on dechlorinating microorganisms. During a field test 280 kg of the iron flakes was injected to a depth of 10–12 m into quaternary sand layers with hydraulic conductivities ranging between 10^?4 and 10^?5 m/s. Fe(0) concentrations of 1 g/kg (sand) or more [up to 100 g/kg (sand)] were achieved in 80 % of the targeted area. The iron flakes have so far remained reactive for more than 1 year and caused a PCE concentration decrease from 20.000–30.000 to 100–200 µg/L. Integration of particle transport processes into the OpenGeoSys model code proved suitable for site-specific 3D prediction and optimization of iron flake injections.     

Salt Crystallization Sequences of Nonmarine Brine and Their Application for the Formation of Potassium Deposits

The salt assemblages precipitated during evaporation of concentrated brine collected from Gasikule Salt Lake (GSL) were studied to better understand the formation of potassium deposits in the Qaidam Basin. The study included isothermal evaporation at 25 °C in the laboratory and solar evaporation in the ponds at GSL field. Brines increased in density and became moderately acidic (pH?≈?5.30) while major ion geochemistry and precipitate mineralogy all showed broad agreement between both systems. Four salt assemblages were identified in the isothermal evaporation experiment: halite?→?halite?+?hexahydrite?→?halite?+?bischofite?+?carnallite?→?bischofite. Alternately, three salt assemblages were recognized in the solar evaporation: halite?→?halite?+?epsomite?+?carnallite?→?halite?+?carnallite?+?bischofite. The key difference in salt assemblages between the two systems is attributed to differences in relative humidity and temperature conditions. Although the GSL has deep spring inflow recharge, the high abundance of MgSO₄ salts demonstrates that the salt assemblages are similar to normal seawater evaporation. Thus, different proportions of deep spring inflow and river water could form both MgSO₄-deficient potassium evaporite and normal seawater potassium evaporites. Therefore, nonmarine water may form diverse potassium evaporite deposits in continental basins when the geological structure as well as hydrogeological and climatic conditions is appropriate.     

Coupling thermodynamic modeling and high-resolution in situ LA-ICP-MS monazite geochronology: evidence for Barrovian metamorphism late in the Grenvillian history of southeastern Ontario

The Flinton Group is a greenschist to upper amphibolite facies package of metasediments in southeastern Ontario that was metamorphosed during the Ottawan Orogeny. Thermodynamic modeling of metapelitic mineral assemblages suggests an increase in peak conditions of metamorphism across the 40 km wide study area from 3.5 to 7.9 kbar and 540 to 715 °C. Garnet isopleth thermobarometry applied to the cores of compositionally zoned porphyroblasts reveals remarkably similar P-T conditions of initial crystallization at approximately 3.7–4.0 kbar and 512–520 °C, corresponding to a relatively high geothermal gradient of ca. 34–45 °C km^?1. It is inferred from modeling and reaction textures that metamorphism was along Barrovian P-T paths. Major and trace element zoning in garnet from one sample records a complex growth history as evidenced by major and trace element zoning and the distribution of xenotime, allanite and monazite inclusions. High-resolution (6 μm) LA-ICP-MS U-Pb geochronology performed on monazite in the rock matrix and included in the outer 150 μm of garnet rim-ward of a Y annulus revealed an age of 976?±?4 Ma. The age is interpreted to reflect monazite growth at the expense of allanite and apatite late in garnet’s growth history over the P-T interval 4.5–6.8 kbar and 540–640 °C. This new age estimate for near peak metamorphism fits well into the regional framework but is significantly younger than previously reported ages for Ottawan metamorphism. Based on microstructures this new age suggests that compressional tectonics were operating much later in the history of the Grenville of southeastern Ontario than previously thought.     

Temporal Changes in Seawater Carbonate Chemistry and Carbon Export from a Southern California Estuary

Estuaries are important subcomponents of the coastal ocean, but knowledge about the temporal and spatial variability of their carbonate chemistry, as well as their contribution to coastal and global carbon fluxes, are limited. In the present study, we measured the temporal and spatial variability of biogeochemical parameters in a saltmarsh estuary in Southern California, the San Dieguito Lagoon (SDL). We also estimated the flux of dissolved inorganic carbon (DIC) and total organic carbon (TOC) to the adjacent coastal ocean over diel and seasonal timescales. The combined net flux of DIC and TOC (F_DIC?+?TOC) to the ocean during outgoing tides ranged from ??1.8±0.5?×?10³ to 9.5±0.7?×?10³?mol C h^?1 during baseline conditions. Based on these fluxes, a rough estimate of the net annual export of DIC and TOC totaled 10±4?×?10⁶?mol C year^?1. Following a major rain event (36 mm rain in 3 days), F_DIC?+?TOC increased and reached values as high as 29.0 ±?0.7?×?10³?mol C h^?1. Assuming a hypothetical scenario of three similar storm events in a year, our annual net flux estimate more than doubled to 25 ±?4?×?10⁶?mol C year^?1. These findings highlight the importance of assessing coastal carbon fluxes on different timescales and incorporating event scale variations in these assessments. Furthermore, for most of the observations elevated levels of total alkalinity (TA) and pH were observed at the estuary mouth relative to the coastal ocean. This suggests that SDL partly buffers against acidification of adjacent coastal surface waters, although the spatial extent of this buffering is likely small.     

Hydraulic conductivity distribution in crystalline rocks, derived from inflows to tunnels and galleries in the Central Alps, Switzerland

Inflow data from 23 tunnels and galleries, 136 km in length and located in the Aar and Gotthard massifs of the Swiss Alps, have been analyzed with the objective (1) to understand the 3-dimensional spatial distribution of groundwater flow in crystalline basement rocks, (2) to assess the dependency of tunnel inflow rate on depth, tectonic overprint, and lithology, and (3) to derive the distribution of fracture transmissivity and effective hydraulic conductivity at the 100-m scale. Brittle tectonic overprint is shown to be the principal parameter regulating inflow rate and dominates over depth and lithology. The highest early time inflow rate is 1,300 l/s and has been reported from a shallow hydropower gallery intersecting a 200-m wide cataclastic fault zone. The derived lognormal transmissivity distribution is based on 1,361 tunnel intervals with a length of 100 m. Such interval transmissivities range between 10^?9 and 10^?1 m²/s within the first 200–400 m of depth and between 10^?9 and 10^?4 m²/s in the depth interval of 400–1,500 m below ground surface. Outside brittle fault zones, a trend of decreasing transmissivity/hydraulic conductivity with increasing depth is observed for some schistous and gneissic geological units, whereas no trend is identified for the granitic units.     

The stability of hydrous phases beyond antigorite breakdown for a magnetite-bearing natural serpentinite between 6.5 and 11 GPa

Phase relations for a natural serpentinite containing 5 wt% of magnetite have been investigated using a multi-anvil apparatus between 6.5 and 11 GPa and 400–850 °C. Post-antigorite hydrous phase assemblages comprise the dense hydrous magnesium silicates (DHMSs) phase A (11.3 wt% H₂O) and the aluminous phase E (Al-PhE, 11.9 wt% H₂O). In addition, a ferromagnesian hydrous silicate (11.1 wt% H₂O) identified as balangeroite (Mg,Fe)₄₂Si₁₆O₅₄(OH)₄₀, typically described in low pressure natural serpentinite, was found coexisting with Al-PhE between 650 and 700 °C at 8 GPa. In the natural antigorite system, phase E stability is extended to lower pressures (8 GPa) than previously reported in simple chemical systems. The reaction Al-phase E?=?garnet?+?olivine?+?H₂O is constrained between 750 and 800 °C between 8 and 11 GPa as the terminal boundary between hydrous mineral assemblages and nominally anhydrous assemblages, hence restricting water transfer into the deep mantle to the coldest slabs. The water storage capacity of the assemblage Al-PhE?+?enstatite (high-clinoenstatite)?+?olivine, relevant for realistic hydrated slab composition along a relatively cold temperature path is estimated to be ca. 2 wt% H₂O. Attempts to mass balance run products emphasizes the role of magnetite in phase equilibria, and suggests the importance of ferric iron in the stabilization of hydrous phases such as balangeroite and aluminous phase E.     

Lead in drinking water and human blood in Riyadh City, Saudi Arabia

Concentrations of lead (Pb) in domestic water and blood plasma in the Olya and Al-Batha regions of Riyadh City, Saudi Arabia were correlated (r ²?=?0.03, p?<?0.0072 and r ²?=?0.37, p?<?0.00092, respectively). Greater concentrations of Pb in domestic water of Olya and Al-Batha (0.0119 and 0.03 mg/l, respectively) were greater than concentrations of Pb in bottled water and was also greater than the concentration of 0.01 mg Pb/l recommended by both the World Health Organization US Environmental Protection Agency (USEPA). In Al-Batha, 52.2 % of the population had concentrations of Pb in blood that exceeded 10 μg Pb/dl, which is the concentration used by USEPA to classify people as being at risk from effects of Pb. In Al-Batha, 17.5 and 22.5 % of the population exceeded 20–40 and >40 μg Pb/dl, respectively. In Olya, 37 and 10 % of the population had concentrations of Pb in blood that exceeded 10 and 20–40 μg Pb/dl, respectively, while none of the concentrations of PB exceeded 40 μg Pb/dl.     

Particle-size effects on dissolved arsenic adsorption to an Australian laterite

In this study, arsenic adsorption to an Australian laterite has been examined for a particle-size range between 38 μm and 25 mm. The results show that particle size influences both kinetic and equilibrium characteristics of arsenic adsorption. The equilibrium adsorption capacity increases from around 100 mg kg^?1 for laterite particles coarser than 4 mm, to around 160 mg kg^?1 for laterite particles between 75 μm and 4 mm, and to over 200 mg kg^?1 for laterite particles finer than 75 μm. The kinetic adsorption data can be fitted with the pseudo-second-order reaction model, in particular for finer particles where the film diffusion and/or surface reaction are important processes. The model-fitted rate constant remains steady for laterite particles coarser than 2 mm, increases moderately with particle size in the range between 75 μm and 2 mm, and increases dramatically for laterite particles finer than 75 μm. These arsenic adsorption behaviours can be explained by the relative importance of two particle-size-dependent processes: quick external-surface adsorption (more important for fine particles) and slow intraparticle adsorption (more important for coarse particles). Most of the external-surface adsorption completes in the first hour of the experiment. To apply the studied laterite for dissolved arsenic removal, it is recommended that fine particles, in particular finer than 75 μm, should be used if the contact time is the limitation, and that coarse particles, in particular 2–4 mm, should be used if sufficient contact time is available.     

Contribution of Viral Lysis and Nanoflagellate Grazing to Bacterial Mortality at Surface Waters and Deeper Depths in the Coastal Ecosystem of Subtropical Western Pacific

Since nanoflagellate grazing and viral lysis differ in their impact on the microbial food web, it is important to assess their relative importance on bacterial mortality fractions. This study investigated the abundance of microbial assemblages and the loss of bacteria due to viral lysis and nanoflagellate grazing at two different depths (3 and 135 m) in the coastal waters of subtropical western Pacific during summer (July, August, and September 2012). The bacterial growth rates in the surface waters varied from 0.07 to 0.09 h^?1, a range higher than those found in the deep waters (0.013 to 0.016 h^?1). The grazing rates of nanoflagellates on bacteria ranged from 0.051 to 0.058 h^?1 and from 0 to 0.004 h^?1 in the surface and deep waters, respectively. During the study period, nanoflagellate grazing was responsible for most of bacterial mortality (81–87 %) relative to viral lysis in the surface waters, while viral lysis was responsible for 67–75 % of the total bacterial mortality in the deep waters.     

Defects in sodalite-group minerals determined from X-ray-induced luminescence

The luminescence spectra of a suite of natural sodium framework silicates including four different sodalite variants and tugtupite have been collected during X-ray irradiation as a function of temperature between 20 and 673 K. The origin of the emission bands observed in these samples is attributed to F-centres (360 nm), paramagnetic oxygen defects (400 and 450 nm), S₂ ^? ions (620 nm) and tetrahedral Fe³⁺ (730 nm). Luminescence in the yellow (550 nm) is tentatively attributed to Mn²⁺, and red luminescence in Cr-rich pink sodalite is possibly from Cr³⁺ activation. Sudden reduction in luminescence intensities of emission centres was observed for all minerals in the 60–120 K range. Since it is common to all the sodalite-group minerals, we infer it is a feature of the aluminosilicate framework. Sodalite luminescence has responses from substitutions on the framework (e.g. paramagnetic oxygen defects, Fe³⁺) which give sodalite properties akin to other framework silicates such as feldspar and quartz. However, the presence of the sodalite cage containing anions (such as F-centres, S₂ ^? ions) imparts additional properties akin to alkali halides. The possibility of coupling between Fe³⁺ and S₂ ^? is discussed. The overall luminescence behaviour of sodalite group can be understood in terms of competition between these centre types.     

Age and paragenesis of mineralisation at Coronation Hill uranium deposit,Northern Territory,Australia

Coronation Hill is a U?+?Au?+?platinum group elements deposit in the South Alligator Valley (SAV) field in northern Australia, south of the better known unconformity-style U East Alligator Rivers (EAR) field. The SAV field differs from the EAR by having a more complex basin-basement architecture. A volcanically active fault trough (Jawoyn Sub-basin) developed on older basement and then was disrupted by renewed faulting, before being buried beneath regional McArthur Basin sandstones that are also the main hanging wall to the EAR deposits. Primary mineralisation at Coronation Hill formed at 1607?±?26 Ma (rather than 600–900 Ma as previously thought), and so it is likely that the SAV was part of a single west McArthur Basin dilational event. Most ore is hosted in sub-vertical faults and breccias in the competent volcanic cover sequence. This favoured fluid mixing, acid buffering (forming illite) and oxidation of Fe²⁺ and reduced C-rich assemblages as important uranium depositional mechanisms. However, reduction of U in fractured older pyrite (Pb model age of 1833?±?67 Ma) is an important trap in diorite. Some primary ore was remobilised at 675?±?21 Ma to form coarse uraninite?+?Ni-Co pyrite networks containing radiogenic Pb. Coronation Hill is polymetallic, and in this respect resembles the ‘egress’-style U deposits in the Athabascan Basin (Canada). However, these are all cover-hosted. A hypothesis for further testing is that Coronation Hill is also egress-style, with ores formed by fluids rising through basement-hosted fault networks (U reduction by diorite pyrite and carbonaceous shale), and into veins and breccias in the overlying Jawoyn Sub-basin volcano-sedimentary succession.     

Calibration of a Bio-optical Model in the North River, North Carolina (Albemarle–Pamlico Sound): A Tool to Evaluate Water Quality Impacts on Seagrasses

Seagrasses are typically light limited in many turbid estuarine systems. Light attenuation is due to water and three optically active constituents (OACs): nonalgal particulates, phytoplankton, and colored dissolved organic matter (CDOM). Using radiative transfer modeling, the inherent optical properties (IOPs) of these three OACs were linked to the light attenuation coefficient, K _PAR, which was measured in North River, North Carolina, by profiles of photosynthetically active radiation (PAR). Seagrasses in the southern portion of Albemarle-Pamlico Estuarine System (APES), the second largest estuary in the USA, were found to be light limited at depths ranging from 0.87 to 2 m. This corresponds to a range of K _PAR from 0.54 to 2.76 m^?1 measured during a 24-month monitoring program. Turbidity ranged from 2.20 to 35.55 NTU, chlorophyll a from 1.56 to 15.35 mg m^?3, and CDOM absorption at 440 nm from 0.319 to 3.554 m^?1. The IOP and water quality data were used to calibrate an existing bio-optical model, which predicted a maximum depth for seagrasses of 1.7 m using annual mean water quality values and a minimum light requirement of 22% surface PAR. The utility of this modeling approach for the management of seagrasses in the APES lies in the identification of which water quality component is most important in driving light attenuation and limiting seagrass depth distribution. The calibrated bio-optical model now enables researchers and managers alike to set water quality targets to achieve desired water column light requirement goals that can be used to set criteria for seagrass habitat protection in North Carolina.