Organohalogen contaminants in finless porpoises (Neophocaena phocaenoides) from Korean coastal waters: Contamination status, maternal transfer and ecotoxicological implications

Information on the occurrence of organochlorine compounds (OCs) and polybrominated diphenyl ethers (PBDEs) in marine mammals from Korea is scarce. In this study, OCs and PBDEs were determined in the blubber of 52 finless porpoises (Neophocaena phocaenoides) from Korean coastal waters. The highest contamination was found for DDTs, followed by PCBs, PBDEs, HCHs, CHLs and HCB. Concentrations of OCs in finless porpoises were lower than those reported worldwide, but PBDE contamination was comparable to other studies, due to ongoing use of PBDE products in Korea. Significant gender-specific differences were found for concentrations and accumulation profiles of OCs and PBDEs, due to maternal transfer and lactation of mature females. The BDEs 49 and 66 comprised 4-16% of total PBDEs in finless porpoises, which seems to be associated with debromination of higher BDEs. The DDT levels in Korean finless porpoises have almost reached the levels associated with immunosuppression in marine mammals.     

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新疆北部地区的大地化学背景

大地化学背景是一种区域地球化学背景。计算深度为地壳最上部的沉积构造层。根据现有的地质学、地球物理学、地球化学和地理学资料,新疆北部地区的面积857000km²,沉积构造层平均厚度为13.9km,其质量为3.13×10¹⁶t.在沉积构造层模型和岩石化学资料基础上,计算和研究了新疆北部地区沉积构造层的平均化学成分和元素丰度。大地化学背景比地壳和岩石圈的化学背景具有更高肯定性。其背景值对区域成矿分析和矿产资源总量评价以及环境质量分析和评估等工作,具有更大的实用价值。本文给出新疆北部地区各大地构造单元的大地化学背景。     

The Air-Sea Exchange of CO2 in the East Sea (Japan Sea)

During CREAMS expeditions, fCO₂ for surface waters was measured continuously along the cruise tracks. The fCO₂ in surface waters in summer varied in the range 320–440 μatm, showing moderate supersaturation with respect to atmospheric CO₂. In winter, however, fCO₂ showed under-saturation of CO₂ in most of the area, while varying in a much wider range from 180 to 520 μatm. Some very high fCO₂ values observed in the northern East Sea (Japan Sea) appeared to be associated with the intensive convection system developed in the area. A gas-exchange model was developed for describing the annual variation of fCO₂ and for estimating the annual flux of CO₂ at the air-sea interface. The model incorporated annual variations in SST, the thickness of the mixed layer, gas exchange associated with wind velocity, biological activity and atmospheric concentration of CO₂. The model shows that the East Sea releases CO₂ into the atmosphere from June to September, and absorbs CO₂ during the rest of the year, from October through May. The net annual CO₂ flux at the air-sea interface was estimated to be 0.032 (±0.012) Gt-C per year from the atmosphere into the East Sea. Water column chemistry shows penetration of CO₂ into the whole water column, supporting a short turnover time for deep waters in the East Sea. This revised version was published online in August 2006 with corrections to the Cover Date.     

Mantle heterogeneity beneath the Antarctic–Phoenix Ridge off Antarctic Peninsula

Abstract   We determined the Sr, Nd and Pb isotopic compositions of basalts recovered from the Antarctic–Phoenix Ridge (APR), a fossil spreading center in the Drake Passage, Antarctic Ocean, in order to understand the nature of the subridge mantle source. There are no known hotspots in close proximity to the site. We observe that small-scale isotopic heterogeneity exists at a shallow level in the subaxial mantle of the APR. Enriched (E-type) mid-ocean ridge basalts (MORB) coexist with normal (N-type) MORB in this region. The E-type basalts are: (i) relatively young compared to the N-type samples; (ii) were erupted after the extinction of the APR; and (iii) have been generated by low-degree partial melting of an enriched mantle source. Extinction of the APR likely caused the extent of partial melting in this region to decrease. We interpret that the geochemically enriched materials dispersed in the ambient depleted mantle were the first fraction to melt to form the E-type MORB.     

Thermally induced brittle deformation in oceanic lithosphere and the spacing of fracture zones

Brittle deformation of oceanic lithosphere due to thermal stress is explored with a numerical model, with an emphasis on the spacing of fracture zones. Brittle deformation is represented by localized plastic strain within a material having an elasto-visco-plastic rheology with strain softening. We show that crustal thickness, creep strength, and the rule governing plastic flow control the formation of cracks. The spacing of primary crack decreases with crustal thickness as long as it is smaller than a threshold value. Creep strength shifts the threshold such that crust with strong creep strength develops primary cracks regardless of crustal thicknesses, while only a thin crust can have primary cracks if its creep strength is low. For a thin crust, the spacing of primary cracks is inversely proportional to the creep strength, suggesting that creep strength might independently contribute to the degree of brittle deformation. Through finite versus zero dilatation in plastic strain, associated and non-associated flow rule results in nearly vertical and V-shaped cracks, respectively. Changes in the tectonic environment of a ridge system can be reflected in variation in crustal thickness, and thus related to brittle deformation. The fracture zone-free Reykjanes ridge is known to have a uniformly thick crust. The Australian-Antarctic Discordance has multiple fracture zones and thin crust. These syntheses are consistent with enhanced brittle deformation of oceanic lithosphere when the crust is thin and vice versa.     

Preliminary health risk assessment for polybrominated diphenyl ethers and polybrominated dibenzo-p-dioxins/furans in seafood from Guangzhou and Zhoushan, China

Dietary intake is one of the important routes of human exposure to brominated flame retardants (BFRs) such as polybrominated diphenyl ethers (PBDEs). The use of PBDEs may also result in exposure to polybrominated dibenzo-p-dioxins and dibenzofurans (PBDDs/DFs), as these compounds are impurities in technical mixtures of BFRs and can also be formed unintentionally by the same processes that generate chlorinated dioxins. This study determined the concentrations of polybrominated compounds in common seafood in Guangzhou and Zhoushan, and assessed the health risks of these chemicals via consumption of contaminated seafood. Seafood samples (fish, bivalves, shrimp, crab, and cephalopods) purchased from local markets in 2003 and 2004 were analyzed for PBDEs and PBDDs/DFs. The highest concentration of total PBDEs (46.3 ng g⁻¹ lipid wt.) was detected in fish from Guangzhou, in which BDEs 47 and 209 were the two predominant congeners. The total daily intakes of PBDEs, PBDDs, and PBDFs were, 946, 6.39, and 6.54 pg kg⁻¹ body weight (bw) in Guangzhou, and 489, 4.99, and 7.65 pg kg⁻¹ bw in Zhoushan, respectively. The hazard ratios for PBDDs and PBDFs were both greater than unity, indicating that these compounds may pose some health risks to the local population.     

Origin and evolution of two contrasting thermal groundwaters (CO2-rich and alkaline) in the Jungwon area,South Korea: Hydrochemical and isotopic evidence

In the Jungwon area, South Korea, two contrasting types of deep thermal groundwater (around 20–33 °C) occur together in granite. Compared to shallow groundwater and surface water, thermal groundwaters have significantly lower δ¹⁸O and δD values (> 1‰ lower in δ¹⁸O) and negligible tritium content (mostly < 2 TU), suggesting a relatively high age of these waters (at least pre-thermonuclear period) and relatively long subsurface circulation. However, the hydrochemical evolution yielded two distinct water types. CO₂-rich water (P_CO2 = 0.1 to 2 atm) is characterized by lower pH (5.7–6.4) and higher TDS content (up to 3300 mg/L), whereas alkaline water (P_CO2 = 10^− 4.1–10^− 4.6 atm) has higher pH (9.1–9.5) and lower TDS (< 254 mg/L). Carbon isotope data indicate that the CO₂-rich water is influenced by a local supply of deep CO₂ (potentially, magmatic), which enhanced dissolution of silicate minerals in surrounding rocks and resulted in elevated concentrations of Ca²⁺, Na⁺, Mg²⁺, K⁺, HCO₃⁻ and silica under lower pH conditions. In contrast, the evolution of the alkaline water was characterized by a lesser degree of water–rock (granite) interaction under the negligible inflow of CO₂. The application of chemical thermometers indicates that the alkaline water represents partially equilibrated waters coming from a geothermal reservoir with a temperature of about 40 °C, while the immature characteristics of the CO₂-rich water resulted from the input of CO₂ in Na–HCO₃ waters and subsequent rock leaching.