Residues of 14C-4n-nonylphenol in mosquitofish (Gambusia holbrooki) oocytes and embryos during dietary exposure of mature females to this xenohormone

In order to assess in fish the maternal transfer of alkylphenolic compounds to the progeny, the identification and quantification of the labelled compounds present in oocytes and embryos was conducted after dietary exposure of mature female mosquitofish to 14C-4n-nonylphenol during vitellogenesis and embryogenesis respectively. Radioactivity found in bile and liver extracts accounted for 0.9-0.6 and 0.2-0.1% of ingested radioactivity for females exposed during vitellogenesis and embryogenesis respectively. The amount of extractable radioactivity present in oocytes and embryos was 0.19 and 0.07% of the ingested dose respectively. The radio-HPLC profiles obtained from bile, liver, oocyte and embryo extracts were similar. They showed the presence of 4n-NP-glucuronide as the major metabolite and traces of unchanged 4n-NP. The other metabolites corresponded to 8-hydroxynonylphenol, 9-(4-hydroxyphenyl)-nonanoic acid and para-hydroxybenzoic acid which is the final product of the alkyl chain oxidation. Our results indicate that exposure of ovoviviparous female fish to 4-NP during vitellogenesis and embryogenesis leads to the contamination of the progeny by 4-NP and its metabolites.     

The influence of particle composition on thorium scavenging in the NE Atlantic ocean (POMME experiment)

²³⁰Th, ²³²Th and ²³⁴Th were analyzed in sinking particles collected by moored and drifting sediment traps in the NE Atlantic Ocean (POMME experiment) in order to constrain the phase(s) carrying Th isotopes in the water column. It reveals a contrasted behaviour between ²³⁴Th and ²³⁰Th. ²³⁴Th is correlated to the particulate organic carbon suggesting that it is primarily scavenged by organic compounds in the surface waters. ²³⁰Th_xs is correlated with Mn, Ba and the lithogenic fraction that are enriched in small suspended particles and incorporated in the sinking particulate flux throughout the water column. The lack of correlation between ²³⁰Th_xs and CaCO₃ or biogenic silica (bSi) indicates that CaCO₃ and bSi are not responsible for ²³⁰Th scavenging in the deep waters of this oceanic region. ²³⁰Th is generally correlated with the lithogenic content of the trapped material but this correlation disappears in winter during strong atmospheric dust inputs suggesting that lithogenic matter is not directly responsible for ²³⁰Th scavenging in the deep waters or that sufficient time is required to achieve particle–solution equilibration. MnO₂ could be the prevalent ²³⁰Th_xs-bearing phase. The narrow range of K_{d_MnO2}^Th obtained for very contrasted oceanic environments supports a global control of ²³⁰Th_xs scavenging by MnO₂ and raises the possibility that the ²³⁰Th–²³¹Pa fractionation is controlled by the amount of colloidal MnO₂ in seawater.     

An experimental study on active tendon control of cable-stayed bridges

Active tendon control of cable-stayed bridges subject to a vertical sinusoidal force is experimentally and analytically studied. Emphasis is placed on the effects of linear and non-linear internal resonances on the control (due to the presence of the cable vibration). A simple cable-supported cantilever beam is used as a model. It is found that active tendon control is very effective in vertical girder motion with small cable vibration (girder dominated motion), whereas it is not effective in vertical girder motion with large cable vibration (cable dominated motion). Analytical prediction is very satisfactory except for the latter case.     

Spectroscopic anatomy of a meteor trail cross section with the European Southern Observatory Very Large Telescope

Abstract— A meteor spectrum was recorded serendipitously at the European Southern Obrervatory (ESO) Very Large Telescope (VLT) during a long exposure in long‐slit spectroscopic mode with FORS1. The ?8 magnitude fireball crossed the narrow 1Î × 7î slit during the observation of a high z supernova in normal service mode operation on May 12, 2002. The spectrum covered the range of 637–1050 nm, where the meteor's air plasma emissions from N₂, N, and O dominate. Carbon atom emission was not detected in the relatively unexplored wavelength range above 900 nm, but the observed upper limit was only 3 sigma less than expected from the dissociation of atmospheric CO₂. The meteor trail was resolved along the slit, and the emission had a Gaussian distribution with a dimension of FWHM = 7.0 (±0.4) * sin(α) * H (km)/90 m, where α is the unknown angle between the orientation of the meteor path and slit and H the assumed altitude of the meteor in km. To our knowledge, this is the first observation of a spatially resolved spectrum across a meteor trail. Unlike model predictions, the plasma excitation temperature varied only from about 4,300 to 4,365 K across the trail, based on the ratio of atomic and molecular nitrogen emissions. Unfortunately, we conclude that this was because the meteor at 100 km altitude was out of focus.     

Pyroxenites from the Southwest Indian Ridge, 9-16{degrees}E: Cumulates from Incremental Melt Fractions Produced at the Top of a Cold Melting Regime

The Southwest Indian Ridge (SWIR) at 9–16°E and 52–53°Sis characterized by ultra-slow, oblique spreading and containsone of the few documented occurrences of pyroxenite veins associatedwith abyssal peridotites. The origin of these uncommon lithologiesis still debated. We present a detailed study (including electronmicroprobe and laser ablation inductively coupled plasma massspectrometry) of spinel websterites collected during Cruise162, Leg 9, of the R.V. Knorr. Rare earth element patterns inclinopyroxenes (Cpx) lead us to discard a possible origin ofthe pyroxenites as residues from partial melting of garnet pyroxenites(i.e. relics of a layered mantle protolith). Their compositionand cumulate texture (when not obscured by mylonitization relatedto emplacement on the seafloor) are better interpreted in termsof fractional crystallization from a basaltic melt at relativelyhigh pressure. Evidence for a high pressure of crystallizationincludes the lack of plagioclase in the cumulate assemblageand the high Al₂O₃ contents of the pyroxenes: up to 5 wt % inorthopyroxene (Opx) and up to 7 wt % in Cpx. These values areamong the highest reported for pyroxenes in a mid-ocean ridgesetting. Sub-solidus breakdown of spinel to plagioclase (nowaltered) is observed in one sample, providing a rough estimateof the final equilibration pressure of these cumulates, around0· 6–0· 7 GPa (plagioclase–spineltransition for a bulk pyroxenite composition). The inferredpyroxenite parent melts were close to equilibrium with the associatedresidual peridotites; some samples have a slightly evolved compositionin terms of the Mg-number [Mg/(Mg + total Fe)]. These parentalmelts had major and trace element compositions consistent witha mid-ocean ridge basalt (MORB) affinity, although they werenot rigorously identical to MORB. Among other characteristics,these melts were relatively depleted in highly incompatibleelements. We propose that they correspond to the latest, shallowest,incremental melt fractions produced during fractional decompressionmelting of a normal MORB (N-MORB) mantle source. These meltsexperienced fractional crystallization as soon as they segregatedfrom the peridotite matrix, moved upward, and crossed the lithosphere–asthenosphereboundary (defined here as the base of the conductive lid). Asa consequence, these shallow melt fractions produced beneathmid-ocean ridges did not fully mix with melt fractions producedand extracted at greater depths. Our study provides concreteevidence for the actuality of pyroxene crystallization in meltchannels beneath mid-ocean ridges at relatively high pressures,a process frequently invoked to account for the ‘pyroxeneparadox’ in MORB petrogenesis. KEY WORDS: abyssal pyroxenites; cumulates; lithospheric mantle; melt migration; Southwest Indian Ridge     

A New Interlaboratory Characterisation of Silicon,Rare Earth Elements and Twenty‐Two Other Trace Element Concentrations in the Natural River Water Certified Reference Material SLRS‐6 (NRC‐CNRC)

The natural river water reference material SLRS‐6 (NRC‐CNRC) is the newest batch of a quality control material routinely used in many international environmental laboratories. This work presents a nine‐laboratory compilation of measurements of major and trace element concentrations and their related uncertainties, unavailable in the NRC‐CNRC certificate (B, Cs, Li, Ga, Ge, Hf, Nb, P, Rb, Rh, Re, S, Sc, Se, Si, Sn, Th, Ti, Tl, W, Y, Y, Zr and REEs). Measurements were mostly made using inductively coupled plasma‐mass spectrometry. The results are compared with equivalent data for the last batch of the material, SLRS‐5, measured simultaneously with SLRS‐6 in this study. In general, very low concentrations, close to the quantification limits, were found in the new batch. The Sr isotopic ratio is also reported.     

Direct Determination of Lead Isotope Ratios by Laser Ablation-Inductively Coupled Plasma-Quadrupole Mass Spectrometry in Lake Sediment Samples

A direct method for the determination of lead isotopic ratios by laser ablation-inductively coupled plasma-quadrupole mass spectrometry (LA-ICP-QMS) is presented. Samples of lake sediments were ground and pressed as pellets before being analysed. Mass bias was corrected by analysing an external calibration sample manufactured with pure silica doped with NIST SRM 981 solution. The efficiency of the mass bias correction was checked by comparing the ICP-MS data with lead isotopic ratios determined by thermal ionisation mass spectrometry (TIMS). The average long term reproducibilities were 0.40%, 0.40%, 0.20% and 0.30% (RSD) respectively for the ²⁰⁶Pb/²⁰⁴Pb, ²⁰⁷Pb/²⁰⁴Pb, ²⁰⁶Pb/²⁰⁷Pb and ²⁰⁸Pb/²⁰⁶Pb ratios. The method was applied to the study of lake sediment samples, in order to determine the amount and origin of historical contamination by lead.