A laboratory study on the kinetics of the formation of oil-suspended particulate matter aggregates using the NIST-1941b sediment

The formation of oil-suspended particulate matter aggregates (OSAs) results from the heteroaggregation between dispersed oil droplets and suspended particulate matter present in coastal waters. This process has been recognized by the oil spill remediation community to enhance natural cleansing of oiled shorelines and oil dispersion in the water column. While several studies have been conducted on the formation and characteristics of OSAs, few studies have addressed the kinetics of OSA formation. Operationally, this has left decision-makers lacking information on the time scale of this process and its significance to oil dispersion in real spills. A laboratory study was conducted to investigate the kinetics of OSA formation as a function of mixing energy and the sediment-to-oil ratio using the standard reference material 1941b. Results showed that formation of OSAs increased exponentially with the mixing time and reached a maximum within 4 h. When the shaking rate increased from 2.0 to 2.3 Hz, the maximum oil trapping efficiency increased from 20% to 42% and the required shaking time decreased from 3.7 to 0.7 h.     

Field validation of antioxidant enzyme biomarkers in mussels (Perna viridis) and clams (Ruditapes philippinarum) transplanted in Hong Kong coastal waters

Green-lipped mussels, Perna viridis, and Manila clams, Ruditapes philippinarum were sourced from “clean” sites in the Hong Kong region, depurated in a laboratory using uncontaminated filtered seawater for 8 days, and transplanted to a suspected gradient of chemically polluted sites in Hong Kong. After 14- and 28-days of field exposure, several antioxidant parameters including glutathione S transferase (GST), catalase (CAT), glutathione peroxidase (GPx), and glutathione (GSH) were quantified in gill and hepatopancreas tissues. Whole body tissue concentrations of polycyclic aromatic hydrocarbons (PAHs), petroleum hydrocarbons (PHCs), polychlorinated biphenyls (PCBs) and organochlorine pesticides (OCs) were determined in pooled site samples. Chemical analyses indicated that: (a) clams had higher levels of PAHs, PHCs, DDTs and PCBs, whereas mussels had higher hexachlorocyclohexane (HCHs) and there was no difference between species for dieldrin and remaining OCs; (b) Kat O should not be continued as a “clean” reference site for Hong Kong, because of the levels of contaminants measured and (c) PAH concentrations in the current survey were similar to those previously measured. Toxicological conclusions were: (a) antioxidant responses were different between species; (b) CAT and GST have highest utility in clams for field use in Hong Kong, whereas CAT in both gill and hepatopancreas tissue showed most potential in mussels; (c) significant induction of antioxidant responses over day 0 (excluding GPx in both tissues, and GST in mussel hepatic tissue); (d) groups of contaminants do not consistently induce antioxidant responses and (e) organochlorines and PCBs correlated significantly with CAT and GST in clam hepatopancreas and with CAT in mussel gill and hepatic tissue. Multivariate statistical techniques indicated little relationship between the site patterns for antioxidant responses and the contaminant gradients identified in body burden analysis.     

The S-type Ladybird leucogranite suite of southeastern British Columbia: Geochemical and isotopic evidence for a genetic link with migmatite formation in the North American basement gneisses of the Monashee complex

The 62–52 Ma Ladybird granite (LBG) suite is a peraluminous, leucocratic, S-type, quartz monzonitic to granitic suite which occurs as batholiths, stocks, dikes, sills, and pegmatite veins predominantly in the high-grade rocks of the Shuswap complex, in southeastern British Columbia. The emplacement of the LBG was synchronous with the production of abundant migmatites within Thor–Odin dome of the Monashee complex, an exposure of North American basement, exhumed from depths of ca. 26–33 km by Eocene extensional faults. The LBG and the leucosome in migmatites from Thor–Odin dome have similar major and trace element patterns, and are both characterized by zircons which have inherited Precambrian cores. Whole rock Nd isotope compositions show a range of values for the LBG with εNd_{(55 Ma)} values from − 5.0 to − 17.2. The εNd_{(55 Ma)} for the leucosome samples range from − 9.5 to − 23.6, overlapping with those of the granitic suite. These data support the interpretation of a genetic link between formation of the LBG suite and melting of North American basement rocks, such as those exposed in the core of Thor–Odin dome. The leucosome samples have lower high field strength element (HFSE) concentrations and positive Eu anomalies, whereas the LBG samples have higher HFSE concentrations and negative Eu anomalies. The similar trace element characteristics suggest that the leucosome from the migmatites and the LBG are related, whereby most of the leucosome samples are cumulates and the LBG samples represent evolved or residual melts. The initial ⁸⁷Sr/⁸⁶Sr isotope values for both the LBG and leucosome samples have a large range. However, the initial Sr isotopic ratios for the LBG suite are lower than those of the leucosome samples, with ⁸⁷Sr/⁸⁶Sr_{(55 Ma)} ranging from 0.70603 to 0.73688 and 0.74256 to 0.76593, respectively. This isotopic discrepancy suggests either: a) isotopic disequilibrium during partial melting in the mid- to lower crust where the leucosome formed, b) the distribution of Sr during partial melting was controlled by different melt-producing reactions, and/or c) isotopic heterogeneity in the source rocks. At least part of the LBG suite likely formed via melting of North American basement rocks that were dominantly of sedimentary origin. Melting of the Proterozoic supracrustal metasedimentary rocks overlying North American basement may also have contributed to the formation of the different phases of the suite found at the regional scale. However, the abundant leucosomes in the basement rocks of Thor–Odin dome may mark the paths along which anatectic melt migrated in the structurally overlying Ladybird granites of the South Fosthall pluton.     

Thallium: A potential guide to mineral deposits

Several recent studies have suggested that rocks associated with mineral deposits of hydrothermal origin are generally enriched in Rb. TI is similar in its geochemical characteristics to Rb, but its use as a potential guide to ore deposits has not been suggested. Although TI has the same size and valency as Rb, it is concentrated more in residual melts than Rb and K because the TI-O bond is more covalent and weaker than either the Rb-O or K-O bonds.A new method which is rapid and precise has been developed by one of the authors for the determination of TI in geological materials at the ppb level. About 350 rocks from 4 mineralized areas in northeastern Washington and central Montana were analyzed for TI by this method. Most of these rocks were also analyzed for SiO₂, A1₂O₃,Fe₂O₃, MgO, CaO, Na₂O, K₂O, TiO₂, P₂O₅, MnO, Ag, As, Au, Ba, Co, Cu, F, Li, Mo, Ni, Pb, Sr, Sb, Sn, Sr, Te, U, W, and Zn. The ore deposits of the areas studied include the gold-silver deposits of the Republic district, the uranium deposit of the Midnite mine, the coppermolybdenum deposit of Mount Tolman, and the gold deposits of the North Moccasin mining district.In all the mineralized areas there is significantly more TI in hydrothermally altered rocks than in unaltered rocks. The very high abundance of TI in the altered rocks of the North Moccasin gold district, and the significant positive correlations of TI and K and TI and Rb in the mineralized rocks of the other three areas suggest that TI was concentrated in hydrothermal fluids. In altered rocks the average K/Rb and K/TI ratios are lower, and the Rb/Sr and TI/Sr ratios are higher.Often the abundance of TI and the K/TI and TI/Sr ratios are more useful in delineating mineralized areas than the abundance of Rb and the K/Rb and Rb/Sr ratios. The ternary relationships between TI and several other elements, especially Rb, K, Ba, and Sr, show mineralized rocks to fall near the TI apices or near the TI-Rb or TI-K boundaries.