Bioconcentration of selected endocrine disrupting compounds in the Mediterranean mussel, Mytilus galloprovincialis

The occurrence of three endocrine disrupting compounds, 4-n-nonylphenol, triclosan and bisphenol A, was investigated in different bivalves originating from the Aegean Sea (Greece). The bioconcentration potential of these compounds was studied using the Mediterranean mussel (Mytilus galloprovincialis). Tissue samples were extracted by sonication. Analysis was performed by gas chromatography-mass spectrometry. According to the field survey results, the average concentrations of 4-n-nonylphenol, triclosan and bisphenol A, were 158, 461 and 404 ng g⁻¹ (dry weight), respectively. During 28 days of exposure at 300 ng L⁻¹, the tissue concentrations of compounds were constantly increased. Steady state was not observed up to the end of the experiment. Kinetic bioconcentration factors varied from 1.7 (4-n-nonylphenol and triclosan) to 4.5 L g⁻¹ (bisphenol A). Following exposure, mussels were relocated to clean water for 28 days. This experiment revealed that depuration rates for all of the target compounds were lower than uptake rates. The biological half-lives of each compound ranged between 12 days (triclosan) and 26 days (bisphenol A).     

Swimming upstream: addressing fossil fuel supply under the UNFCCC

Reducing fossil fuel supply is necessary to meet the Paris Agreement goal to keep warming ‘well below 2°C’, yet the Agreement is silent on the topic of fossil fuels. This article outlines reasons why it is important that Parties to the Agreement find ways to more explicitly address the phasing out of fossil fuel production under the UNFCCC. It describes how countries aiming to keep fossil fuel supply in line with Paris goals could articulate and report their actions within the current architecture of the Agreement. It also outlines specific mechanisms of the Paris Agreement through which issues related to the curtailment of fossil fuel supply can be addressed. Mapping out a transition away from fossil fuels – and facilitating this transition under the auspices of the UNFCCC process – can enhance the ambition and effectiveness of national and international climate mitigation efforts.

Key policy insights

• The international commitment to limit global average temperature increases to ‘well below 2°C’ provides a strong rationale for Parties to the Paris Agreement and the UNFCCC to pursue a phase-down in fossil fuel production, not just consumption.

• Several countries have already made commitments to address fossil fuel supply, by agreeing to phase down coal or oil exploration and production.

• Integrating these commitments into the UNFCCC process would link them to global climate goals, and ensure they form part of a broader global effort to transition away from fossil fuels.

• The Paris Agreement provides a number of new opportunities for Parties to address fossil fuel production.

     

Oxyanion Concentrations in Eastern Sierra Nevada Rivers – 2. Arsenic and Phosphate

Water samples were collected from the Truckee River-Pyramid Lake system, the Walker River-Walker Lake system, and the Carson River, all located in eastern California and western Nevada, U.S.A., at three different times (i.e., summer 1991, spring 1992, and autumn 1992) over a two year period. The concentrations of As, Na, Cl, PO4, and pH were measured in these river samples and the associated terminal lakes. Arsenic values ranged from below 13 nmol/kg near Truckee, California to 160 nmol/kg at Nixon, Nevada in the Truckee River, from 40 nmol/kg in the headwaters of both West and East Walker Rivers to 270 nmol/kg below Weber Reservoir on the main branch of the Walker River, and from <27 nmol/kg to 234 nmol/kg for the lower Carson River system. Arsenic concentrations in Steamboat Creek (0.91 mol/kg–1.80 mol/kg) in the Truckee River catchment are above the U.S. EPA drinking water maximum contaminant level of 0.67 mol/kg, as are the As concentrations in both Pyramid Lake (1.33 mol/kg–1.57 mol/kg ) and Walker Lake (13.7 mol/kg–18.7 mol/kg). Sources of As for all three rivers include weathering of As-rich rocks and/or regolith and input of high-As geothermal spring waters, both processes primarily, although not exclusively, adding As to the headwater regions of these rivers. Steamboat Hot Springs (29 mol/kg As 54.5 mol/kg), for example, is identified as a source of As to the Truckee River via Steamboat Creek. The high As concentrations in Pyramid and Walker Lakes are likely due to (1) desorption of arsenate from aquatic particulate matter in these high pH waters (9.0 pH 9.5), (2) limited biologic uptake of arsenate, and (3) evaporative concentration of the lake waters. Evaluation of molar PO4}/As ratios of river waters and geothermal spring waters (e.g., Steamboat Hot Springs), indicates that phosphate is substantially enriched in Steamboat Creek as well as the mid to lower reaches of the Walker and Carson Rivers. These regions of each river are dominated by agricultural interests and, additionally, in the case of Steamboat Creek, residential areas and golf courses. Our data strongly imply that phosphate-rich agricultural return flow has likely added P to these streams and, consequently, increased their respective P:As ratios.     

Controls on regional variability in marine pore-water diagenesis below the seafloor in Upper Jurassic–Lower Cretaceous prodeltaic sandstone and shales,Scotian Basin,Eastern Canada

Diagenesis in the uppermost Jurassic to Lower Cretaceous deltaic sandstones and shales of the Scotian Basin is an important control on reservoir quality. Ferruginous zone (sub-oxic) marine pore-water diagenesis controls the initial formation of Fe²⁺-silicates that are the precursors of grain-rimming chlorite that preserves porosity. This study assesses the regional controls on the type of marine pore-water diagenesis by studying the sedimentology, mineralogy, and geochemistry of the retrogradational units and underlying progradational units in parasequences from conventional cores in two wells in different parts of the basin. Coated grains preserve a record of whether marine pore-water diagenesis below the seafloor was dominantly in the ferruginous or sulphidic geochemical zone. Four types of coated grain were distinguished, each with a different mineral paragenesis. Mineralogical and chemical evidence of ferruginous zone diagenesis includes the presence of diagenetic chlorite and siderite, and the correlation of P with Fe or Ti. Pyrite and Fe-calcite are found where the sulphidic zone is more significant than the ferruginous zone. Ferruginous zone diagenesis was common in low-sedimentation rate retrogradational sediments with low organic carbon, and in delta-front turbidites and river-mouth sandstones. Estuarine, tidal flat and prodeltaic facies that are directly supplied by riverine sediments have a lower Fe:Ti ratio than do fully marine shoreface and open shelf facies as a result of input of detrital ilmenite and its alteration products. The relative contribution of colloidal iron (hydr)-oxides appears greater in distal low-sedimentation rate environments. Where large changes in sedimentation rate occurred at ravinement surfaces, the underlying progradational rocks have evidence of ferruginous zone diagenesis, whatever their facies. Rapid upward migration of the pore-water profile resulting from the change in sedimentation rate reduced the time available for mineral products to form in the deeper pore-water zones. This study has shown that the availability of Fe and organic carbon varying in a complex manner in marine deltaic sediments, but that the resulting diagenesis by marine pore-water can be predicted from facies and paleogeographic setting.     

Geochemistry, tectonic setting and metamorphism of mid-triassic volcanic rocks of Greece

Mid-Triassic volcanic rocks are preserved in about eight localities in the nappes of the external Hellenides, and are also widespread in the Pelagonian zone of central Greece. Most have suffered low-grade metamorphism. Immobile trace elements from 35 samples, 80 major element analyses, and pyroxene analyses show that these rocks are the product of an eastward dipping subduction zone. The subducted ocean was perhaps analogous to the Pennine zone of the Alps. The Othris and Pindos ophiolites are probably contemporaneous products of related back-arc extension.Metamorphic mineral assemblages in volcanic rocks of the Phyllite Series of the external Hellenides indicate high-pressure, low-temperature conditions, probably related to a second subduction that occurred prior to the main phase of Hellenide nappe emplacement in the Miocene.     

Multiply exsolved clinopyroxene megacrysts from the Frank Smith Mine,Cape Province,South Africa

Two clinopyroxene megacrysts from the Frank Smith kimberlite show multiple exsolution of garnet, orthopyroxene and oxide phases. In one of the megacrysts the lamellar texture has partly recrystallized to a granular one. The chemical compositions of the exsolved phases are similar to those of discrete nodules and of granular pyroxenites found in the same kimberlite. Conditions of formation of the original homogeneous clinopyroxene solid solution are estimated to be ～1500°C and 37 kb, whereas the re-equilibration conditions are closer to 900°C and 35 kb. The megacrysts may have belonged to the Karroo age magnetism which predated kimberlite activity and have been brought to the surface as accidental xenocrysts by the Frank Smith kimberlite.     

The relationship between length and width of plutons within the crustal-scale Cobequid Shear Zone, northern Appalachians, Canada

The lengths and widths have been measured for 69 component bodies of composite plutons along the Cobequid Shear Zone. Plutons on major fault strands, those with mylonite zones >0.1 km wide, exhibit evidence of multiple intrusion of magma batches. Small plutons along short faults in stepover zones appear related to rapid emplacement of magma in bodies 1.5–4 km long by 0.1–2 km wide. Such small plutons show low enrichment in incompatible elements in older component bodies, but increasing amounts in younger bodies as a result of progressive magma expulsion from crystal mush during crystallization and shear-enhanced compaction in fault zones. Wider plutons generally occur along longer fault strands accommodating more strain and penetrating deeper into the crust and show enrichment in incompatible elements. The width of the mylonitic fault zone is about 15% of the width of these plutons. The length-to-width ratio of component bodies and composite plutons varies between 2 and 11. The best-fit line describing these data has a slope of 1.056, which implies scaling behavior between plutonism and tectonic processes. Scalar properties of plutonic bodies are similar to those of faults, but scalar relationships observed in component bodies do not apply to composite plutons.     

Probing the Quiet Solar Atmosphere from the Photosphere to the Corona

We investigate the morphology and temporal variability of a quiet-Sun network region in different solar layers. The emission in several extreme ultraviolet (EUV) spectral lines through both raster and slot time-series, recorded by the EUV Imaging Spectrometer (EIS) on board the Hinode spacecraft is studied along with \(\mbox{H}\upalpha\) observations and high-resolution spectropolarimetric observations of the photospheric magnetic field. The photospheric magnetic field is extrapolated up to the corona, showing a multitude of large- and small-scale structures. We show for the first time that the smallest magnetic structures at both the network and internetwork contribute significantly to the emission in EUV lines, with temperatures ranging from \(8\times 10^{4}~\mbox{K}\) to \(6\times 10^{5}~\mbox{K}\). Two components of transition region emission are present, one associated with small-scale loops that do not reach coronal temperatures, and another component that acts as an interface between coronal and chromospheric plasma. Both components are associated with persistent chromospheric structures. The temporal variability of the EUV intensity at the network region is also associated with chromospheric motions, pointing to a connection between transition region and chromospheric features. Intensity enhancements in the EUV transition region lines are preferentially produced by \(\mbox{H}\upalpha\) upflows. Examination of two individual chromospheric jets shows that their evolution is associated with intensity variations in transition region and coronal temperatures.     

Distinguishing active and legacy source contributions to stream water quality: Comparative quantification for chloride and metals

Hydrochemical constituents in streams may originate from currently active sources at the surface and/or legacy sources from earlier surface inputs, waste deposits and land contamination. Distinction and quantification of these source contributions are needed for improved interpretation of tracer data and effective reduction of waterborne environmental pollutants. This article develops a methodology that recognizes and quantifies some general mechanistic differences in stream concentration and load behavior versus discharge between such source contributions. The methodology is applied to comparative analysis of stream concentration data for chloride (Cl⁻), copper (Cu), lead (Pb), and zinc (Zn), and corresponding data for water discharge, measured over the period 1990–2018 in multiple hydrological catchments (19 for Cl⁻, 11 for Cu and Zn, 10 for Pb) around the major Lake Mälaren in Sweden. For Cl⁻, the average load fraction of active sources is quantified to be 19%, and the average active and legacy concentration contributions as 2.9 and 11 mg/L, respectively. For the metals, the average active load fractions at outlets are 1%–3% over all catchments and 9%–14% in the relatively few catchments with mixed metal sources. Average active and legacy concentration contributions are 0.14 and 3.2 μg/L for Cu, 0.05 and 1.5 μg/L for Pb, and 1.4 and 12 μg/L for Zn, respectively. This multi-catchment analysis thus indicates a widespread prevalence of legacy sources, with greater legacy than active concentration contributions for both Cl⁻ and the metals, and active contributions playing a greater role for chloride than for the metals. The relatively simple first-order methodology developed and applied in the study can be used to screen commonly available stream monitoring data for possible distinction of active and legacy contributions of any hydrochemical constituent in and across various hydrological catchment settings.     

Nutrient source attribution: Quantitative typology distinction of active and legacy source contributions to waterborne loads

Distinction between active and legacy sources of nutrients is needed for effective reduction of waterborne nutrient loads and associated eutrophication. This study quantifies main typological differences in nutrient load behaviour versus water discharge for active and legacy sources. This quantitative typology is used for source attribution based on monitoring data for water discharge and concentrations of total nitrogen (TN) and total phosphorous (TP) from 37 catchments draining into the Baltic Sea along the coastline of Sweden over the period 2003–2013. Results indicate dominant legacy source contributions to the monitored loads of TN and TP in most (33 of the total 37) study catchments. Dominant active sources are indicated in 1 catchment for TN, and mixed sources are indicated in 3 catchments for TN, and 4 catchments for TP. The TN and TP concentration contributions are quantified to be overall higher from the legacy than the active sources. Legacy concentrations also correlate well with key indicators of human activity in the catchments, agricultural land share for TN (R² = 0.65) and population density for TP (R² = 0.56). Legacy-dominated nutrient concentrations also change more slowly than in catchments with dominant active or mixed sources. Various data-based results and indications converge in indicating legacy source contributions as largely dominant, mainly anthropogenic, and with near-zero average change trends in the present study of catchments draining into the Baltic Sea along the coastline of Sweden, as in other parts of the world. These convergent indications emphasize needs to identify and map the different types of sources in each catchment, and differentiate strategies and measures to target each source type for possible achievement of shorter- and longer-term goals of water quality improvement.