Effect of intertidal compared to subtidal exposure on the uptake,loss and oxidative toxicity of water-born benzo[a]pyrene in the mantle and whole tissues of the mussel,Mytilus edulis L

Blue mussels (Mytilus edulis, L.) were exposed to a single dose of 1 ppb benzo[a]pyrene (BaP) under subtidal (SC) or tidal conditions (TC; 6 h immersion, 6 h emersion) in order to follow its bioaccumulation in whole mussel and mantle tissue, and to compare BaP-mediated toxicity on lipids (malonaldehyde formation, MDA) in the mantle. Rapid uptake of BaP (70-80% of BaP initially introduced in tanks) was observed in both conditions after 12 h, but subsequent depuration in clean water was slower in TC mussels. BaP levels decreased in whole tissue in both conditions between 12 and 24 h, but increased in mantle. The mantle BaP levels were similar during the first 4 days in SC and TC, but whereas they decreased in SC after 7 days. BaP was retained at high levels in mantle in TC until the end of the study (14 days). In both conditions, significant increases (P < 0.05) in lipid peroxidation were observed after 4 days, but MDA levels were approximately 3 times higher in the mantle of TC than SC mussels, although BaP tissue concentrations were similar. These observations suggested that increased BaP-mediated toxicity in mantle lipid was due to the interactive effect of the tidal cycle of immersion/emersion on BaP-mediated oxidative damage.     

Nucleation and growth rates of homogeneously condensing water vapor in argon from shock tube experiments

A special shock tube process combining a reflected expansion wave with a weak shock wave is analyzed and calibrated. The process is employed to transfer water vapor carried in argon into a known supersaturated state for a short period of time (0.5 ms). During that period steady state homogeneous nucleation takes place followed by condensational growth. Nucleation and growth rates are measured by a 90° Mie-light scattering technique in the temperature range 200–260 K. The results are compared with existing theoretical models.     

Variations in population vulnerability to tectonic and landslide-related tsunami hazards in Alaska

Natural Hazards - Effective tsunami risk reduction requires an understanding of how at-risk populations are specifically vulnerable to tsunami threats. Vulnerability assessments primarily have been...     

Hydrothermalism in the Tyrrhenian Sea: Inorganic and microbial sulfur cycling as revealed by geochemical and multiple sulfur isotope data

The Palinuro volcanic complex and the Panarea hydrothermal field, both located in the Tyrrhenian Sea (Italy), are associated with island arc magmatism and characterized by polymetallic sulfide mineralization. Dissolved sulfide concentrations, pH, and Eh measured in porewaters at both sites reveal a variable hydrothermal influence on porewater chemistry.Multiple sulfur isotopic measurements for disseminated sulfides (CRS: chromium reducible sulfur) extracted from sediments at Palinuro yielded a broad range in δ³⁴S range between ?29.8 and + 10.2‰ and Δ³³S values between + 0.015 and + 0.134‰. In contrast, sediments at Panarea exhibit a much smaller range in δ³⁴S_CRS with less negative values between ?11.3 and ?1.8‰. The sulfur isotope signatures are interpreted to reflect a mixture between hydrothermal and biogenic sulfide, with a more substantial biogenic contribution at Panarea.Multiple sulfur isotope measurements were performed on sulfides and elemental sulfur from drill core material from the Palinuro massive sulfide complex. δ³⁴S and Δ³³S values for pyrite between ?32.8 and ?1.1‰ and between ?0.012 to + 0.042‰, respectively, as well as for elemental sulfur with δ³⁴S and Δ³³S values between ?26.7 and ?2.1‰ and between + 0.035 and + 0.109‰, respectively, point to a microbial origin for much of the sulfide and elemental sulfur studied. Moreover, data suggest a coupling of bacterial sulfate reduction, sulfide oxidation and sulfur disproportionation. In addition, δ³⁴S values for barite between + 25.0 and + 63.6‰ are also in agreement with high microbial turnover of sulfate at Palinuro.Although a magmatic SO₂ contribution towards the formation of the Palinuro massive sulfide complex is very likely, the activity of different sulfur utilizing microorganisms played a fundamental role during its formation. Thus, porewater and multiple sulfur isotope data reveal differences in the hydrothermal activity at Palinuro and Panarea drill sites and underline the importance of microbial communities for the origin of massive sulfide mineralizations in the hydrothermal subsurface.     

Macroscale friction of granular soils under monotonic and cyclic loading based upon micromechanical determination of dissipated energy

Macroscopic frictional behavior of granular materials is of great importance for studying several complex problems associated with fault slip and landslides. The main objective of this study is to model the macroscale frictional behavior of granular soils under monotonic and cyclic loadings based upon micromechanical determination of dissipated energy at particle contacts. This study is built on the general observation that the externally computed energy dissipation should be equal to the total internal energy dissipation derived from inter-particle sliding and rolling, energy losses from inter-particle collisions, and damping. For this purpose, the discrete element method is used to model a granular soil and determine the stored, dissipated, and damping energies associated with shear loading for applied monotonic and cyclic velocities. These energies are then related to the friction by an application of the Taylor-critical state power balance relationship. Also, the contributions of the different modes of energy dissipation (normal, shear, and rolling) to the total frictional resistance were studied. By changing the inter-particle friction, the simulations showed that the macroscopic friction was nearly constant, the slip friction increased almost linearly with increasing inter-particle friction, and the difference between the two was attributed to the non-energy dissipating dilatancy component. By providing a clear relationship between energy dissipated by micro-scale mechanisms versus the traditional engineering definition based on macro-scale (continuum) parameters, this study provides a means to develop a better understanding for the frictional behavior of granular media.

     

The atmospheric transport potential for water vapour and dust in the Sahel region

The transport of water vapour and dust in the Sahel can be assigned to identical atmospheric flow systems, the African Easterly Jet, the Easterly Waves and the Squall Lines. The yield of the rainy season in the Sahel depends on the conditions in the preceding rains of the season and is closely coupled to the surface heat budget both in the monsoonal air in the S and the trades in the N. The heat budget, in particular the evaporation after the passage of a Squall Line, is influenced not only by the total amount of preceding rains but also by the plant cover pumping the water to the surface and smoothing the magnitude of the evaporation in time. This feed-back mechanism may be made responsible for the persistence of the Sahel drought as experienced in recent years. The dust export from the African continent towards the Atlantic can only be so effective, because the Squall Lines and the African Easterly Jet are meshed in a way that produces large amounts of suspended material and lifts it to great heights where the transport velocity is very fast.     

High pressure single-crystal synthesis, structure and compressibility of the garnet Mn2+ 3Mn3+ 2[SiO4]3

Single crystals of the garnet Mn²⁺ ₃Mn³⁺ ₂[SiO₄]₃ and coesite were synthesised from MnO₂-SiO₂ oxide mixtures at 1000°C and 9 GPa in a multianvil press. The crystal structure of the garnet [space group Ia3¯d, a=11.801(2) Å] was refined at room temperature and 100 K from single-crystal X-ray data to R1=2.36% and R1=2.71%, respectively. In contrast to tetragonal Ca₃Mn³⁺ ₂[GeO₄]₃ (space group I4₁/a), the high-pressure garnet is cubic and does not display an ordered Jahn-Teller distortion of octahedral Mn³⁺. A disordered Jahn-Teller distortion either dynamic or static is evidenced by unusual high anisotropic displacement parameters. The room temperature structure is characterised by following bond lengths: Si-O=1.636(4) Å (tetrahedron), Mn³⁺-O=1.995 (4) Å (octahedron), Mn²⁺-O=2.280(5) and 2.409(4) Å (dodecahedron). The cubic structure was preserved upon cooling to 100 K [a=11.788(2) Å] and upon compressing up to 11.8 GPa in a diamond-anvil cell. Pressure variation of the unit cell parameter expressed by a third-order Birch-Murnaghan equation of state led to a bulk modulus K ₀=151.6(8) GPa and its pressure derivatives K′=6.38(19). The peak positions of the Raman spectrum recorded for Mn²⁺ ₃Mn³⁺ ₂[SiO₄]₃ were assigned based on a calderite Mn²⁺ ₃Fe³⁺ ₂[SiO₄]₃ model extrapolated from andradite and grossular literature data.     

Chemical Separation of Tungsten and Other Trace Elements for TIMS Isotope Ratio Measurements Using Organic Acids

One requirement for isotope ratio measurement results with small measurement uncertainties is that the element of interest is effectively separated from the sample matrix. Efficient chemical separation of W from matrix components, especially Ti, can be challenging, particularly for large test portion masses (> 1 g). We present a new W separation procedure that takes advantage of the distinct complexation behaviour of Ti and W with citrate ligand in a moderately low pH, oxidising solution. This preparation procedure can reduce the Ti/W ratio of large (4–10 g) basaltic (i.e., high‐matrix) test portions by a factor of 10⁵, relative to their original compositions, in a two‐step separation procedure. The procedure additionally provides a separate, well‐purified Mo fraction. We show that optimal separation requires precise selection of reagent concentrations and sample load. The procedure was employed to determine the μ¹⁸²W composition of BHVO‐2 as ?6.7 ± 4.2 (2 standard deviation, 2s). The principles derived from this method may prove useful for chemical separation of other elements used for geochemical and cosmochemical applications given an appropriate selection of organic acid. Future successful applications of this method may reveal that the use of organic acids as procedural reagents is a currently under‐utilised tool for efficient chemical separation protocols.     

Holocene records of eolian dust deposition from high-elevation lakes in the Uinta Mountains,Utah, USA

Radiocarbon-dated sediment cores from subalpine lakes were used to investigate post-glacial dust deposition in the Uinta Mountains (Utah, USA). Lake sediments were geochemically characterized with ICP-OES, ICP-MS and XRF core scanning. Collections from passive samplers constrain the properties of modern dust, and samples of regolith constrain properties of the local material within the watershed. Ca and Eu are more abundant in dust, whereas Ti and Zr are more abundant in local regolith. As a result, the Ca/Ti and Eu/Zr ratios are indices for the dust content of lake sediment. In all records, the dust index rises in the early Holocene as watersheds became stabilized with vegetation, reducing the influx of local material. After this point, values remained above average through the middle Holocene, consistent with an increased dust content in the sediment. Dust index values drop in the late Holocene in most lakes, suggesting a decrease in dust abundance. Generally synchronous shifts in dust index values in cores from lakes in different parts of this mountain range are evidence of enhanced dust deposition in this region during the middle Holocene, and are consistent with a variety of records for increased aridity in the south-western USA at this time.