Effect of bioemulsificant exopolysaccharide (EPS2003) on microbial community dynamics during assays of oil spill bioremediation: A microcosm study

Microcosms experiments were carried out to evaluate the effect of bioemulsificant exopolysaccharide (EPS₂₀₀₃) on microbial community dynamics. An experimental seawater microcosm, supplemented with crude oil and EPS₂₀₀₃ (SW + OIL + EPS₂₀₀₃), was monitored for 15 days and compared to control microcosm (only oil-polluted seawater, SW + OIL). Determination of bacterial abundance, heterotrophic cultivable and hydrocarbon-degrading bacteria were carried out during all experimentation period. The microbial community dynamic was monitored by isolation of total RNA, RT-PCR amplification of 16S rRNA, cloning and sequencing. Oil degradation was monitored by GC–MS analysis. Bioemulsificant addition stimulated an increase of the total bacterial abundance, change in the community structure and activity. The bioemulsificant also increased of 5 times the oil biodegradation rate.The data obtained from microcosm experiment indicated that EPS₂₀₀₃ could be used for the dispersion of oil slicks and could stimulate the selection of marine hydrocarbon degraders thus increasing bioremediation process.     

Strong climate and tectonic control on plagioclase weathering in granitic terrain

Investigations to understand linkages among climate, erosion and weathering are central to quantifying landscape evolution. We approach these linkages through synthesis of regolith data for granitic terrain compiled with respect to climate, geochemistry, and denudation rates for low sloping upland profiles. Focusing on Na as a proxy for plagioclase weathering, we quantified regolith Na depletion, Na mass loss, and the relative partitioning of denudation to physical and chemical contributions. The depth and magnitude of regolith Na depletion increased continuously with increasing water availability, except for locations with mean annual temperature < 5 °C that exhibited little Na depletion, and locations with physical erosion rates < 20 g m^? 2 yr^? 1 that exhibited deep and complete regolith Na depletion. Surface Na depletion also tended to decrease with increasing physical erosion. Depth-integrated Na mass loss and regolith depth were both three orders of magnitude greater in the fully depleted, low erosion rate sites relative to other locations. These locations exhibited strong erosion-limitation of Na chemical weathering rates based on correlation of Na chemical weathering rate to total Na denudation. Sodium weathering rates in cool locations with positive annual water balance were strongly correlated to total Na denudation and precipitation, and exhibited an average apparent activation energy (Ea) of 69 kJ mol^? 1 Na. The remaining water-limited locations exhibited kinetic limitation of Na weathering rates with an Ea of 136 kJ mol^? 1 Na, roughly equivalent to the sum of laboratory measures of Ea and dissolution reaction enthalpy for albite. Water availability is suggested as the dominant factor limiting rate kinetics in the water-limited systems. Together, these data demonstrate marked transitions and nonlinearity in how climate and tectonics correlate to plagioclase chemical weathering and Na mass loss.     

Forsterite to wadsleyite phase transformation under shear stress and consequences for the Earth's mantle transition zone

We have studied the phase transformation of forsterite to wadsleyite under shear stress at the Earth's transition zone pressure and temperature conditions. Two-step experiments were performed using a multi-anvil press. First, we hot pressed iron-free forsterite at 6 or 11 GPa and 1100 °C. Then we deformed a slab of this starting material using a direct simple shear assembly at 16 GPa and 1400 °C for 1, 15, 35, 40, or 60 min. Both the starting material and the deformed samples were characterized using optical and scanning electron microscopy including measurements of crystal preferred orientations (CPO) by electron back scattered diffraction (EBSD), transmission electron microscopy (TEM), and Fourier transform infrared spectroscopy (FTIR). The phase transformation occurs very rapidly, in less than 1 min, and metastable forsterite relics are not observed after deformation. The grain size of wadsleyite is slightly smaller than the forsterite starting material. The water contents obtained from FTIR analyses in forsterite and wadsleyite are 65–124 wt ppm H₂O and 114–736 wt ppm H₂O, respectively, which are well below water solubility at similar conditions in the presence of free water. Wadsleyite aggregates display weak CPO patterns with [1 0 0] axes concentrated at low angle to the shear direction, [0 1 0] axes perpendicular to the shear plane and nearly random [0 0 1] axes. Only a few dislocations were observed in wadsleyite with TEM. This observation is consistent with the assumption that most dislocations formed during the initial high-stress stages of these stress-relaxation experiments, were consumed in the phase transformation, probably enhancing the transformation rate. CPO patterns vary as a function of the water content: with increasing water content the density of [1 0 0] axes parallel to the shear direction decreases, and the density of [0 0 1] axes increases. Viscoplastic self-consistent modeling of CPO evolution using previously reported glide systems for wadsleyite, i.e., [1 0 0]{0 k l} and 1/2 〈1 1 1〉{1 0 1}, cannot reproduce the measured CPO, unless the [0 0 1](0 1 0) system, for which dislocations have not been observed by TEM, is also activated. In addition, wadsleyite grain growth suggests the participation of diffusion-assisted processes in deformation. Calculated anisotropies for P and S-waves using measured CPO are always below 1%. This very low anisotropy is due to both the low finite strain achieved in the experiments, which leads to weak wadsleyite CPO, and to the diluting effect of added majorite. The present experiments emphasize the importance of stress, grain size evolution and water content in the forsterite to wadsleyite phase transformation and subsequent deformation in the transition zone.     

Molybdenum isotope signatures in continental margin marine sediments

We present molybdenum isotope data for four sediment profiles from continental margin settings. Each profile has a distinctive average isotope composition ranging from δ^98 / 95Mo − 0.5‰ to 1.3‰ (relative to J and M laboratory standard). This range lies between the modern ocean water value (2.3‰) and the values typical of Mo adsorbed onto Mn oxides (− 0.7‰ ± 0.1‰). An important finding of this study is the apparent co-variation between the Mo isotope composition and the accumulation rate of authigenic Mo under reducing conditions. This relationship suggests that the chemical processes responsible for Mo accumulation under reducing conditions produce an isotope signature in marine sediments. In addition to the relationship between Mo accumulation and the Mo isotope signature there is also a relationship between these parameters and the rate of organic carbon oxidation and burial. These relationships suggest that the Mo isotope signature of reducing sediments may serve as a tracer for the cycling of organic carbon in continental margin sediments; however, additional data will be required to refine any such relationships.     

Isotopic fractionation of zinc in tektites

Tektites are terrestrial natural glasses produced during a hypervelocity impact of an extraterrestrial projectile onto the Earth's surface. The similarity between the chemical and isotopic compositions of tektites and terrestrial upper continental crust implies that the tektites formed by fusion of such target rock. Tektites are among the driest rocks on Earth. Although volatilization at high temperature may have caused this extreme dryness, the exact mechanism of the water loss and the behavior of other volatile species during tektite formation are still debated. Volatilization can fractionate isotopes, therefore, comparing the isotope composition of volatile elements in tektites with that of their source rocks may help to understand the physical conditions during tektite formation.For this study, we have measured the Zn isotopic composition of 20 tektites from four different strewn fields. Almost all samples are enriched in heavy isotopes of Zn compared to the upper continental crust. On average, the different groups of tektites are isotopically distinct (listed from the isotopically lightest to the heaviest): Muong-Nong type indochinites (δ^66/64Zn = 0.61 ± 0.30‰); North American bediasites (δ^66/64Zn = 1.61 ± 0.49‰); Ivory Coast tektites (δ^66/64Zn = 1.66 ± 0.18‰); the Australasian tektites (others than the Muong Nong-type indochinites) (δ^66/64Zn = 1.84 ± 0.42‰); and Central European moldavites (δ^66/64Zn = 2.04 ± 0.19‰). These results are contrasted with a narrow range of δ^66/64Zn = 0–0.7‰ for a diverse spectrum of upper continental crust materials.The elemental abundance of Zn is negatively correlated with δ^66/64Zn, which may reflect that isotopic fractionation occurred by evaporation during the heating event upon tektite formation. Simple Rayleigh distillation predicts isotopic fractionations much larger than what is actually observed, therefore, such a model cannot account for the observed Zn isotope fractionation in tektites. We have developed a more realistic model of evaporation of Zn from a molten sphere: during its hypervelocity trajectory, the molten surface of the tektite will be entrained by viscous coupling with air that will then induce a velocity field inside the molten sphere. This velocity field induces significant radial chemical mixing within the tektite that accelerates the evaporation process. Our model, albeit parameter dependent, shows that both the isotopic composition and the chemical abundances measured in tektites can be produced by evaporation in a diffusion-limited regime.     

Does heavy oil pollution induce bacterial diseases in Japanese flounder Paralichthys olivaceus?

As basic research for the effect of heavy oil on the fish immune system, in this study, the number of leukocyte was counted in Japanese flounder Paralichthys olivaceus, after exposure to heavy oil at a concentration of 30 g/8 L for 3 days. To compare the numbers of bacteria in the skin mucus between oil-exposed and control fish, viable bacteria were enumerated by counting colony forming unit (CFU). Compared with 5.79 ± 1.88 × 10⁷ leukocytes/mL in the controls, the exposed fish demonstrated higher counts, averaging 1.45 ± 0.45 × 10⁸ cells/mL. The bacterial numbers of control fish were 4.27 ± 3.68 × 10⁴ CFU/g, whereas they were 4.58 ± 1.63 × 10⁵ CFU/g in the exposed fish. The results suggest that immune suppression of the fish occurred due to heavy oil stressor, and bacteria could invade in the mucus, resulting in the increasing leukocyte number to prevent infectious disease.     

Characteristics and role of groundwater dissolved organic matter on arsenic mobilization and poisoning in Bangladesh

The fluorescence and molecular weight characteristics of dissolved organic matter (DOM) in groundwater of Bangladesh were investigated to evaluate its multiple roles on arsenic (As) mobilization and poisoning. Fluorescence properties of DOM were measured in groundwater samples collected from two As contaminated areas of Bangladesh (Faridpur at the Ganges floodplain and Sonargaon at the Meghna floodplain) from different locations and depths. The three dimensional excitation–emission matrix (3DEEM) fluorescence spectra of groundwater samples showed two characteristic peaks around Ex/Em = 335–365 nm/435–480 nm for fulvic-like peaks and peak at around Ex/Em = 275–290 nm/310–335 nm for the protein-like materials. The similarity of fluorescence spectra of groundwater and surface water of both the study areas with high intensity of fluorescence and its strong correlation with DOC reflect the in situ generation of fluorescent DOM from sedimentary organic matter (SOM) and recent recharge of terrestrial labile organic carbon into shallow aquifer. High performance size-exclusion chromatography (HPSEC) analysis of DOM shows positive correlations between fluorescence intensities (FI) of small molecular fractions (0.65 kDa) and As concentrations, with the signatures of protein-like peaks of DOM in groundwater. This result provides new evidence that small molecular weight fraction of DOM in groundwater of Bangladesh can play an important role on As mobilization and toxicity. In addition, high concentration of fluorescence materials in DOM of As contaminated groundwater of Bangladesh may pose a threat to public health.     

PAHs contamination and bacterial communities in mangrove surface sediments of the Jiulong River Estuary,China

Sixteen sediment samples collected from eight transects in a mangrove swamp of the Jiulong River Estuary, Fujian, China were investigated for their content of polycyclic aromatic hydrocarbons (PAHs) and the biodegradation potential of the indigenous microorganisms. The bacterial community structures in the mangrove sediments and in enrichment cultures were also investigated. The results showed that the total PAHs concentration of mangrove sediments ranged from 280 to 1074 ng g⁻¹ dry weight, that the PAHs composition pattern in the mangrove sediments was dominated by high molecular weight PAH components (4–6 rings), and that Benzo[ghi]perylene and Indeno[1,2,3-cd]pyrene were the most dominant at different stations. Abundant PAH-degrading bacteria were found in all the stations, the values of phenanthrene-degrading bacteria ranged from 5.85 × 10⁴ to 7.80 × 10⁵ CFU g⁻¹ dry weight, fluoranthene-degrading bacteria ranged from 5.25 × 10⁴ to 5.79 × 10⁵ CFU g⁻¹ dry weight, pyrene-degrading bacteria ranged from 3.10 × 10⁴ to 6.97 × 10⁵ CFU g⁻¹ dry weight and the benzo(a)pyrene-degrading bacteria ranged from 5.25 × 10⁴ to 7.26 × 10⁵ CFU g⁻¹ dry weight. DGGE analysis of PCR-amplified 16S rDNA gene fragments confirmed that there was a remarkable shift in the composition of the bacterial community due to the addition of the different model PAH compound phenanthrene (three ring PAH), fluoranthene(four ring PAH), pyrene(four ring PAH) and benzo(a)pyrene(five ring PAH) during enrichment batch culture. Eleven strains were obtained with different morphology and different degradation ability. The presence of common bands for microbial species in the cultures and in the native mangrove sediment DNA indicated that these strains could be potential in situ PAH-degraders.     

Cenozoic changes in atmospheric lead recorded in central Pacific ferromanganese crusts

The possible sources of pre-anthropogenic Pb contributed to the world's oceans have been the focus of considerable study. The role of eolian dust versus riverine inputs has been of particular interest. With better calibration of isotopic records from central Pacific ferromanganese crusts using Os isotope stratigraphy it now appears that deep water Pb isotopic compositions were effectively homogeneous over a distance of 5000 km for the past 80 Myr. The composition shifted slightly from high ²⁰⁶Pb/²⁰⁴Pb ratios in the range of 18.87 ± 0.02 before 65 Ma to lower values of 18.62 ± 0.02 by 45 Ma and then gradually increased again very slightly to the present day ratio of 18.67 ± 0.02. The regional homogeneity provides evidence of a dominant well-mixed atmospheric source the most likely candidate for which is volcanic aerosols contributed either directly or as soluble condensates on eolian dust. The slight shift in Pb isotope composition of deep waters in the central Pacific between 65 and 45 Ma may be the result of a regional- or perhaps global-scale change in the sources of volcanic exhalations and volcanic activity caused by an increase in the importance of melting and assimilation of older continental crustal components over the Cenozoic.     

Tracking the lithium isotopic evolution of the mantle using carbonatites

Carbonatites are mantle-derived, intraplate magmas that provide a means of documenting isotopic variations of the Earth's mantle through time. To investigate the secular Li isotopic evolution of the mantle and to test whether Li isotopes document systematic recycling of material processed at or near the Earth's surface into the mantle, we analyzed the Li isotopic compositions of carbonatites and spatially associated mafic silicate rocks. The Li isotopic compositions of Archean (2.7 Ga) to Recent carbonatites (δ⁷Li = 4.1 ± 1.3 (n = 23, 1σ)) overlap the range typical for modern mantle-derived rocks, and do not change with time, despite ongoing crustal recycling. Thus, the average Li isotopic composition of recycled crustal components has not deviated greatly from the mantle value (~ + 4) and/or Li diffusion is sufficiently fast to attenuate significant heterogeneities over timescales of 10⁸ years. Modeling of Li diffusion at mantle temperatures suggests that limited δ⁷Li variation in the mantle through time reflects the more effective homogenization of Li in the mantle compared to radiogenic isotope systems. The real (but limited) variations in δ⁷Li that exist in modern mantle-derived magmas as well as carbonatites studied here may reflect isotopic fractionation associated with shallow-level processes, such as crustal assimilation and diffusive isotopic fractionation in magmatic systems, with some of the scatter possibly related to low-temperature alteration.     

Thermal history and origin of the Tanzanian Craton from Pb isotope thermochronology of feldspars from lower crustal xenoliths

Common and radiogenic Pb isotopic compositions of plagioclase and anti-perthitic feldspars from granulite-facies lower crustal xenoliths from the Labait Volcano on the eastern margin of the Tanzanian Craton have been measured via laser ablation MC-ICP-MS. Common Pb in plagioclase and a single stage Pb evolution model indicate that the lower crust of the Tanzanian Craton was extracted from mantle having a ²³⁸U/²⁰⁴Pb of 8.1 ± 0.3 and a ²³²Th/²³⁸U of 4.3 ± 0.1 at 2.71 ± 0.09 Ga (all uncertainties are 2σ). Since 2.4 Ga, some orthoclase domains within anti-perthites have evolved with a maximum ²³⁸U/²⁰⁴Pb of 6 and ²³²Th/²³⁸U of 4.3. The spread in Pb isotopic composition in the anti-perthitic feldspars yields single crystal Pb–Pb isochrons of ～ 2.4 Ga, within uncertainty of U–Pb zircon ages from the same sample suite. The Pb isotopic heterogeneities imply that these granulites resided at temperatures < 600 °C in the lower crust of the Tanzanian Craton from ca. 2.4 Ga to the present. In concert with the chemistry of surface samples, mantle xenoliths, and lower crustal xenoliths, our data imply that the cratonic lithosphere in Tanzania formed ca. ～ 2.7 Ga, in a convergent margin setting, and has remained undisturbed since 2.7 Ga.     

Optical signatures of dissolved organic matter in the watershed of a globally large river (Yangtze River,China)

Parallel factor analysis of fluorescence excitation emission matrices of surface water samples of a globally large river (Yangtze River, China) watershed identified three classes of fluorescent dissolved organic matter (FDOM) that had ex/em = 280/330 nm, 305/385 nm and 350/450 nm respectively, resembling “peak T”, “peak M” and “peak C” commonly identified in natural water, respectively. Peak T (a tyrosine/tryptophan-like FDOM) did not show correlations to peak M or C which were humic-like substances, while a positive correlation (r = 0.935, p < 0.001) was present between the natural log-transformed maximum fluorescence intensity (F_max) of peaks T and M indicating a tight link during their production and processing. F_max values (in Raman unit nm^?1) normalized to dissolved organic carbon (DOC) concentration were low, varying in ranges 15.93–85.95, 29.83–83.54 and 19.73–51.05 × 10^?5 nm^?1 (μmol/L)^?1 for peaks T, M and C, respectively, in line with the history of strong photobleaching of the water samples as indicated by fairly high absorption spectral slope ratios (0.75–1.53 with a mean 1.03). Intermediate fluorescence index (FI) (1.46–1.83 with a mean 1.61) and small specific absorption at 254 nm (0.64–1.93 with a mean 1.15 m^?1 mg^?1 L) of the water samples, indicated the presence of both aquatic microbial DOM (e.g. peak T) and soil DOM (e.g. peak C). Peak C could be substantially removed by UV-A (320–400 nm) irradiation, while peak M was slightly increased when a microbe-containing water was exposed to the same UV-A irradiation. Taken together, peak C was attributed to diffuse soil source while peak M was likely attributed to joint effects of microbial activities and solar irradiation on the chromophores in the sample.     

Hf and Nd isotopes in marine sediments: Constraints on global silicate weathering

The combined use of Lu–Hf and Sm–Nd isotope systems potentially offers a unique perspective for investigating continental erosion, but little is known about whether, and to what extent, the Hf–Nd isotope composition of sediments is related to silicate weathering intensity. In this study, Hf and Nd elemental and isotope data are reported for marine muds, leached Fe-oxide fractions and zircon-rich turbidite sands collected off the Congo River mouth, and from other parts of the SE Atlantic Ocean. All studied samples from the Congo fan (muds, Fe-hydroxides, sands) exhibit indistinguishable Nd isotopic composition (ε_Nd ~ ? 16), indicating that Fe-hydroxides leached from these sediments correspond to continental oxides precipitated within the Congo basin. In marked contrast, Hf isotope compositions for the same samples exhibit significant variations. Leached Fe-hydroxide fractions are characterized by ε_Hf values (from ? 1.1 to + 1.3) far more radiogenic than associated sediments (from ? 7.1 to ? 12.0) and turbidite sands (from ? 27.2 to ? 31.6). ε_Hf values for Congo fan sediments correlate very well with Al/K (i.e. a well-known index for the intensity of chemical weathering in Central Africa). Taken together, these results indicate that (1) silicate weathering on continents leads to erosion products having very distinctive Hf isotope signatures, and (2) a direct relationship exists between ε_Hf of secondary clay minerals and chemical weathering intensity.These results combined with data from the literature have global implications for understanding the Hf–Nd isotope variability in marine precipitates and sediments. Leached Fe-hydroxides from Congo fan sediments plot remarkably well on an extension of the ‘seawater array’ (i.e. the correlation defined by deep-sea Fe–Mn precipitates), providing additional support to the suggestion that the ocean Hf budget is dominated by continental inputs. Fine-grained sediments define a diffuse trend, between that for igneous rocks and the ‘seawater array’, which we refer to as the ‘zircon-free sediment array’ (ε_Hf = 0.91 ε_Nd + 3.10). Finally, we show that the Hf–Nd arrays for seawater, unweathered igneous rocks, zircon-free and zircon-bearing sediments (ε_Hf = 1.80 ε_Nd + 2.35) can all be reconciled, using Monte Carlo simulations, with a simple weathering model of the continental crust.     

Geologic evolution of the Donguinyó-Huichapan caldera complex,central Mexican Volcanic Belt,Mexico

The Donguinyó-Huichapan caldera complex is located 110 km to the NNW of Mexico City, in the central sector of the Mexican Volcanic Belt. It is a 10 km in diameter complex apparently with two overlapping calderas, each one related to an ignimbrite sequence that contrasts in composition, mineralogy, welding, distribution, and physical aspect. The geologic evolution of this complex includes the following phases, 1) A first caldera formed at 5.0 ± 0.3 Ma, with the eruption of several discrete pulses of andesitic to trachydacitic pyroclastic flows that produced a series of densely welded ignimbrites; 2) At 4.6 ± 0.3 Ma, several small shield volcanoes and cinder cones built the rim of this caldera and erupted basaltic-andesite and andesitic lava flows; 3) At 4.2 ± 0.2 Ma, a second caldera was formed associated to the eruption of the Huichapan Tuff, which is a rhyolitic pyroclastic sequence consisting of minor unwelded ignimbrites, pumice fall and surge deposits, and a voluminous welded ignimbrite; 4) Also yielding an age of 4.2 ± 0.2 Ma, several trachydacitic lava domes were extruded along the new ring fracture and formed the rim of the Huichapan caldera, as well as five intra-caldera domes of dacitic and trachydacitic composition. Peripheral volcanism includes a large 2.5 ± 0.1 Ma shield volcano that was emplaced on the Huichapan caldera rim.The two calderas that form the Donguinyó-Huichapan complex have contrasting differences in volcanic styles that were apparently due to their differences in composition. Products erupted by the Donguinyó caldera are basaltic-andesite to trachydacitic in composition, whereas Huichapan caldera products are all high-silica rhyolites.     

Formation of the Late Permian Panzhihua plutonic-hypabyssal-volcanic igneous complex: Implications for the genesis of Fe–Ti oxide deposits and A-type granites of SW China

The Late Permian (260 Ma) Emeishan large igneous province of SW China contains numerous magmatic Fe–Ti oxide deposits. The Fe–Ti oxide deposits occur in the lower parts of evolved layered gabbroic intrusions which are spatially and temporally associated with A-type granitic rocks. The 260 Ma Panzhihua layered gabbroic intrusion hosts one of the largest magmatic Fe–Ti oxide deposits in China and is coeval with a peralkaline A-type granitic pluton. The granite has intruded the overlying Emeishan flood basalts and fed at least one dyke which erupted onto the surface producing columnar jointed trachytes. The presence of syenodiorite between the layered gabbro and granite is evidence for compositional evolution from mafic to intermediate to felsic rocks. The syenodiorites have intermediate to felsic composition with SiO₂ = 61 to 65 wt.%, MgO = 0.27 to 0.6 wt.% and CaO = 1.0 to 2.5 wt.% as compared to the granite SiO₂ = 65 to 72 wt.%, MgO = 0.1 to 0.4 wt.%, CaO = < 1.0 wt.%. Primitive-mantle-normalized incompatible element plots show corresponding reciprocal patterns between the mafic and felsic rocks. The chondrite-normalized REE patterns show Eu anomalies changing from > 1(Eu/Eu? = 1.1 to 2.6) in the gabbroic intrusion, to < 1 in the syenodiorite (Eu/Eu? = 0.75 to 0.83), granites and trachytes (Eu/Eu? = 0.55–0.87). Previously published εNd_(T) values from clinopyroxenes (εNd_(T) = + 1.1 to + 3.2) of the gabbroic intrusion match the whole-rock values of the syenodiorite (εNd_(T) = + 2.1 to + 2.5), granite and trachyte (εNd_(T) = + 2.2 to + 2.9), suggesting that all rock types originated from the same mantle source. MELTS and trace element modeling confirm that all rock types can be generated by fractional crystallization of high-Ti Emeishan basalt. The jump in SiO₂ from the gabbro to the syenodiorite is attributed to the en masse crystallization of the Fe–Ti oxides. The geological and geochemical data indicate that fractional crystallization of a common parental magma produced the layered gabbroic intrusion and Fe–Ti oxide deposit, the syenodiorite, granites and trachyte of the Panzhihua region, which thus form a genetically related plutonic-hypabyssal-volcanic complex. Other granite–gabbro complexes in the region likely formed in a similar manner.     

Source heterogeneity for the major components of ∼ 3.7 Ga Banded Iron Formations (Isua Greenstone Belt,Western Greenland): Tracing the nature of interacting water masses in BIF formation

We report trace element, samarium (Sm)–neodymium (Nd) and lead (Pb) isotopic data for individual micro-and mesobands of the Earth's oldest Banded Iron Formation (BIF) from the ∼ 3.7–3.8 Ga Isua Greenstone Belt (IGB, West Greenland) in an attempt to contribute to the characterization of the depositional environment and to the understanding of depositional mechanisms of these earliest chemical sediments. Rare earth element (REE)-yttrium (Y) patterns of the individual mesobands show features of modern seawater with diagnostic cerium (Ce/Ce^⁎), presodymium (Pr/Pr^⁎) and Y/holmium (Ho) anomalies. Very low high field strength elements (HFSE) concentrations indicate essentially detritus-free precipitation. Uranogenic Pb isotope data define a correlation line with a slope of 3691 ± 41 Ma, indicating that the uranium (U)–lead (Pb) system remained closed after the formation of this BIF. High ²⁰⁷Pb/²⁰⁴Pb relative to ²⁰⁶Pb/²⁰⁴Pb ratios compared to average mantle growth evolution models are a feature shared by BIF, penecontemporaneous basalts and clastic volcanogenic metasediments and are indicative of the ultimate high-μ (²³⁸U/²⁰⁴Pb) character of the source region, an essentially mafic Hadean protocrust. Sm–Nd isotopic relations on a layer-by-layer basis point to two REE sources controlling the back-arc basin depositional environment of the BIF, one being seafloor-vented hydrothermal fluids (εNd (3.7 Ga) ∼ + 3.1), the other being ambient surface seawater which reached its composition by erosion of parts of the protocrustal landmass (εNd(3.7 Ga) ∼ + 1.6). The validity of two different and periodically interacting water masses (an essentially two-component mixing system) in the deposition of alternating iron- and silica-rich layers is also reflected by systematic trends in germanium (Ge)/silicon (Si) ratios. These suggest that significant amounts of silica were derived from unexposed and/or destroyed mafic Hadean landmass, unlike iron which probably originated from oceanic crust following hydrothermal alteration by deep percolating seawater. Ge/Si distributional patterns in the early Archean Isua BIF are similar to those reported from the Paleoproterozoic Hamersley (Western Australia) BIF, but overall Ge concentrations are about one order of magnitude higher in the Archean BIF. This seems consistent with other lines of evidence that the ambient Archean seawater was enriched with iron relative to Proterozoic and recent seawater.     

Two extraterrestrial dust horizons found in the Dome Fuji ice core,East Antarctica

Two silicate-rich dust layers were found in the Dome Fuji ice core in East Antarctica, at Marine Isotope Stages 12 and 13. Morphologies, textures, and chemical compositions of constituent particles reveal that they are high-temperature melting products and are of extraterrestrial origin. Because similar layers were found ～ 2000 km east of Dome Fuji, at EPICA (European Project for Ice Coring in Antarctica)-Dome C, particles must have rained down over a wide area 434 and 481 ka. The strewn fields occurred over an area of at least 3 × 10⁶ km². Chemical compositions of constituent phases and oxygen isotopic composition of olivines suggest that the upper dust layer was produced by a high-temperature interaction between silicate-rich melt and water vapor due to an impact explosion or an aerial burst of a chondritic meteoroid on the inland East Antarctic ice sheet. An estimated total mass of the impactor, on the basis of particle flux and distribution area, is at least 3 × 10⁹ kg. A possible parent material of the lower dust layer is a fragment of friable primitive asteroid or comet. A hypervelocity impact of asteroidal/cometary material on the upper atmosphere and an explosion might have produced aggregates of sub-μm to μm-sized spherules. Total mass of the parent material of the lower layer must exceed 1 × 10⁹ kg. The two extraterrestrial horizons, each a few millimeters in thickness, represent regional or global meteoritic events not identified previously in the Southern Hemisphere.     

Determining the dispersibility of South Louisiana crude oil by eight oil dispersant products listed on the NCP Product Schedule

We recently conducted a laboratory study to measure the dispersion effectiveness of eight dispersants currently listed on the National Contingency Plan Product Schedule. Results are useful in determining how many commercial dispersant products would have been effective for use on South Louisiana crude oil in the Deepwater Horizon oil spill. The test used was a modification of the Baffled Flask Test (BFT), which is being proposed to replace the current Swirling Flask Test (SFT). The modifications of the BFT in this study included use of one oil rather than two, increasing replication from 4 runs to 6, and testing at two temperatures, 5 °C and 25 °C. Results indicated that temperature was not as critical a variable as the literature suggested, likely because of the low viscosity and light weight of the SLC. Of the eight dispersants tested, only three gave satisfactory results in the laboratory flasks at both temperatures.     

Re–Os geochronology of a Mesoproterozoic sedimentary succession,Taoudeni basin,Mauritania: Implications for basin-wide correlations and Re–Os organic-rich sediments systematics

The exceptionally well-preserved sedimentary rocks of the Taoudeni basin, NW Africa represent one of the world's most widespread (> 1 M km²) Proterozoic successions. Hitherto, the sedimentary rocks were considered to be Mid Tonian based on Rb–Sr illite and glauconite geochronology of the Atar Group. However, new Re–Os organic-rich sediment (ORS) geochronology from two drill cores indicates that the Proterozoic Atar Group is ～ 200 Ma older (1107 ± 12 Ma, 1109 ± 22 Ma and 1105 ± 37 Ma). The Re–Os geochronology suggests that the Rb–Sr geochronology records the age of diagenetic events possibly associated with the Pan African collision.The new Re–Os geochronology data provide absolute age constraints for recent carbon isotope chemostratigraphy which suggests that the Atar Group is Mesoproterozoic and not Neoproterozoic.The new Re–Os ORS geochronology supports previous studies that suggest that rapid hydrocarbon generation (flash pyrolysis) from contact metamorphism of a dolerite sill does not significantly disturb the Re–Os ORS systematics. Modelled contact conditions suggest that the Re–Os ORS systematics remain undisturbed at ～ 650 °C at the sill/shale contact and ≥ 280 °C 20 m from the sill/shale contact.Moreover, the Re–Os geochronology indicates that the West African craton has a depositional history that predates 1100 Ma and that ORS can be correlated on a basin-wide scale. In addition, the Re–Os depositional ages for the ORS of the Taoudeni basin are comparable to those of ORS from the São Francisco craton, suggesting that these cratons are correlatable. This postulate is further supported by identical Os_i values for the Atar Group and the Vazante Group of the São Francisco craton.     

Optical properties and light penetration in a deep,naturally acidic,iron rich lake: Lago Caviahue (Patagonia,Argentina)

The optical properties and light climate in the deep and extremely acid Lake Caviahue have been studied in order to better understand its characteristics and the possible influence upon the phytoplankton community. The absorption coefficients for the dissolved fraction were maximal in the ultraviolet (UV) region and the water absorption spectra showed a shoulder around 300 nm, which was attributed to the concentration of Fe(III). No radiation was detected in the water column below 360 nm. The depth of the 1% incident radiation was dependent of wavelength, showing its maximum of 13.3 m at 565 nm, compared to 1.7 m and 4.8 m at 400 nm and 700 nm, respectively. Phytoplankton biomass was low and showed an almost constant profile with depth despite the relative darkness of the water column. Optical climate of Lake Caviahue is not typical of high elevation lakes but is more similar to low elevation shallow lakes of the Andean region. The chemical composition of the water, mainly Fe oxidation state and concentration, is the responsible for the high attenuation of the UV radiation (UVR). Living organisms are protected of UVR because Lake Caviahue waters are a shield against UV-B.