Iron isotope fractionation in subterranean estuaries

Dissolved Fe concentrations in subterranean estuaries, like their river-seawater counterparts, are strongly controlled by non-conservative behavior during mixing of groundwater and seawater in coastal aquifers. Previous studies at a subterranean estuary of Waquoit Bay on Cape Cod, USA demonstrate extensive precipitation of groundwater-borne dissolved ferrous iron and subsequent accumulation of iron oxides onto subsurface sands. Waquoit Bay is thus an excellent natural laboratory to assess the mechanisms of Fe-isotope fractionation in redox-stratified environments and determine potential Fe-isotope signatures of groundwater sources to coastal seawater. Here, we report Fe isotope compositions of iron-coated sands and porewaters beneath the intertidal zone of Waquoit Bay. The distribution of pore water Fe shows two distinct sources of Fe: one residing in the upward rising plume of Fe-rich groundwater and the second in the salt-wedge zone of pore water. The groundwater source has high Fe(II) concentration consistent with anoxic conditions and yield δ⁵⁶Fe values between 0.3 and −1.3‰. In contrast, sediment porewaters occurring in the mixing zone of the subterranean estuary have very low δ⁵⁶Fe values down to −5‰. These low δ⁵⁶Fe values reflect Fe-redox cycling and result from the preferential retention of heavy Fe-isotopes onto newly formed Fe-oxyhydroxides. Analysis of Fe-oxides precipitated onto subsurface sands in two cores from the subterranean estuary revealed strong δ⁵⁶Fe and Fe concentration gradients over less than 2m, yielding an overall range of δ⁵⁶Fe values between −2 and 1.5‰. The relationship between Fe concentration and δ⁵⁶Fe of Fe-rich sands can be modeled by the progressive precipitation of Fe-oxides along fluid flow through the subterranean estuary. These results demonstrate that large-scale Fe isotope fractionation (up to 5‰) can occur in subterranean estuaries, which could lead to coastal seawater characterized by very low δ⁵⁶Fe values relative to river values.     

Regulation of Tilapia metallothionein gene expression by heavy metal ions

Tilapia is a common fish species inhabiting inland waters and estuarine regions in Hong Kong and Southeast Asia, and useful for bio-monitoring of metal pollution. Metallothionein (MT) gene expression in fish tissues has been useful to sub-lethal risk assessment as biomarker of exposure to metal ions in fishes inhabiting metal contaminated area. To investigate metal inductions of Tilapia MT gene expression in vivo, Tilapias were injected with different concentrations of heavy metals and tissues were then removed for quantitative PCR assay using mimic PCR methods. All of the metal ions tested (Cu(2+), Cd(2+), Hg(2+), Ni(2+), Pb(2+) and Zn(2+)) were able to induce hepatic MT mRNA levels. Renal MT mRNA levels of Cd(2+) and Zn(2+) treated fish was not induced with significant fold induction, however MT mRNA levels in gills were sensitive to the administrations of these metal ions. These data indicated that Tilapia MT mRNA levels in gills and liver are sensitive biomarker of exposure to various metal ions.     

Relationships between tissue concentrations of chlorinated hydrocarbons (polychlorinated biphenyls and chlorinated pesticides) and antioxidative responses of marine mussels, Perna viridis

Marine mussels, Perna viridis, were transplanted from a reference site to various polluted sites around Hong Kong. After 30 d of exposure, antioxidative responses in the gills and hepatopancreas and tissue concentrations of chlorinated hydrocarbons [polychlorinated biphenyls (PCBs) and chlorinated pesticides (CPs)] were determined for individual mussels. Glutathione S transferase (GST) and glutathione (GSH) were positively correlated with tissue PCB concentrations. Only one of the enzymatic antioxidants, glutathione peroxidase (GPx), showed significant response to tissue PCB. No significant correlation was found between tissue concentrations of chlorinated hydrocarbons and other enzymatic antioxidants (superoxide dismutase (SOD), catalase (CAT), glutathione reductase (GR) and NADPH DT-diaphorase (DT-d). Oxidative stress, measured as thiobarbituric acid reactive substances, was correlated with chlorinated pesticide concentrations in tissues. This study demonstrated a correlation between GST/GSH and chlorinated hydrocarbons. The apparent lack of correlation between trace organic pollutants and some of the enzymatic antioxidants may be due to the inhibitory effects caused by these chemicals. The above results suggest that more investigations are needed before these enzymes can be used as biomarkers.     

Mathematical modeling of PCB bioaccumulation in Perna viridis

In the present work, we built a mathematical model of polychlorinated biphenyl (PCB) bioaccumulation in Perna viridis, namely, a one-compartment model with a time dependent incorporation rate R (μg g⁻¹ lipid per ppb water per day), with positive substrate cooperativity as the underlying physical mechanism. The temporal change of the PCB concentration Q (μg g⁻¹ lipid) in the soft tissues of the mussel depends on the competition of the input rate RW and the output rate kQ, where W is the concentration of PCB in water (ppb water) and k is the elimination rate (per day). From our experimental data, k=0.181±0.017 d⁻¹. The critical concentration in water W_c for positive substrate cooperativity was found to be 2.4 ppb. Below W_c, R is a constant. For a water concentration of 0.5 ppb Aroclor 1254, R=24.0±2.4 μg g⁻¹ lipid ppb⁻¹ d⁻¹. Above W_c, positive substrate cooperativity comes into effect and R becomes a function of time and dependent on the concentration Q in a form R=γQ/(Q+δ). This is the case for a water concentration of 5 ppb Aroclor 1254, where γ=15.1 μg g⁻¹ lipid ppb⁻¹ d¹ and δ≈200 μg g⁻¹ lipid. From this model, the uptake is exponentially increasing when the PCB concentration in the mussel is small compared to 200 μg g⁻¹ lipid, and hyperbolically increasing when the concentration is large compared to 200 μg g⁻¹ lipid, which are consistent with the experimental data. The model is useful for understanding the true processes taking place during the bioaccumulation and for risk assessment with higher confidence. Future experimental data which challenge the present model are anticipated and in fact desirable for improvement and perfection of the model.     

Relationships between natural terrain landslide magnitudes and triggering rainfall based on a large landslide inventory in Hong Kong

Rain-induced landslides are recognized as one of the most catastrophic hazards on hilly terrains. To develop strategies for landslide risk assessment and management, it is necessary to estimate not only the rainfall threshold for the initiation of landslides, but also the likely magnitudes of landslides triggered by a storm of a given intensity. In this study, the frequency distributions of both open hillside landslides and channelized debris flows in Hong Kong are established on the basis of the Enhanced Natural Terrain Landslide Inventory (ENTLI) with 19,763 records in Hong Kong up to 2013. The landslide magnitudes are measured in terms of the number, scar area, volume, or density of landslides. The mean values of the scar areas and volumes are 55.2 m² and 102.0 m³, respectively, for the open hillside landslides and 91.3 m² and 166.5 m³, respectively, for the channelized debris flows. Empirical correlations between the numbers, scar areas, and volumes of hillside landslides or channelized debris flows and the maximum rolling rainfall intensities of different periods have been derived. The maximum rolling 4- to 24-h rainfall amounts provide better predictions compared with those with the maximum rolling 1-h rainfall. Maximum rolling rainfall intensity-duration thresholds identifying the likely rainfall conditions that yield natural terrain landslides or debris flows of different magnitudes are also proposed. The initiation rainfall thresholds are identified as 75, 90, 100, 120, 150, 180, and 200 mm for the maximum rolling 1-, 2-, 4-, 6-, 8-, 12-, and 24-h rainfall, respectively.     

Early-Holocene geochemical evolution of saline Medicine Lake,South Dakota

Medicine Lake is a highly saline, meromictic, magnesium sulfate, closed-basin lake in northeastern South Dakota. The geochemical, mineralogical, and magnetic stratigraphies of sediments deposited from about 10.8 to 4.5 ka B.P. document the evolution of the saline brine in response to climatic change in the early to mid-Holocene. During the spruce occupation of the Medicine Lake catchment (10.8–10.0 ka B.P.), dark-grey massive basal sediments with low total-sulfur and carbonate content, upwardly increasing organic-carbon content, and high magnetic susceptibility were deposited in a deep freshwater lake. As the vegetation in the area changed from spruce to birch to oak and elm and finally to prairie between 10.0 and 9.2 ka B.P., and as the lake became shallow and salinity increased from <2 to >10%, light-and dark-grey calcareous and organic-carbon-rich banded sediments with low total-sulfur content and low magnetic susceptibility were deposited. Previous studies have shown that during the forest/prairie transition the lake then changed abruptly from fresh to saline as it lost a substantial portion of its volume. During the early prairie period (9.2–5.5 ka B.P.), alternating sections of aragonite-rich laminae and grey massive sediments with high total-sulfur content and multiple gypsum layers were deposited in a meromictic environment under conditions of fluctuating lake levels and salinity. Continued aridity during the mid-Holocene (5.5–4.5 ka B.P.) probably maintained the lake at relatively low levels and high salinity as dark-grey generally massive sediments with moderate total-sulfur, carbonate, and organic-carbon content and no measurable magnetic susceptibility were deposited.     

A new interpretation of measured ionic diffusion coefficient in compacted bentonite-based materials

Previous model based on free-water properties to interpret the measured diffusion coefficient in compacted bentonite-based materials is demonstrated to be inadequate. A model considering ionic diffusion in clay surface (bound) and interstitial (free) water is presented to interpret the measured diffusion coefficients and to explain the possible reasons for the discrepancies in the data. The measured diffusion coefficient is determined by the predominant diffusion pathway, which depends on the charge of diffusing species, soil fabric, diffusion time and by the starting concentration condition of the method used.     

用超速CT机检测99例无症状香港中国人降低钙指数

回顾分析Ｍａｔｉｌｄａ医院超速ＣＴ室筛选首批病人中９９例中国人资料，很明显从通常采用１３０－１００Ｈｏｕｎｓｆｉｅｌｄ单位作为检出冠状血管钙化的基数应用至中国人身上其阈值数目需要降低，同时，我们也发现如果病人年龄按每１０年范围分组（２１－３０，３０－４０，４１－５０，５１－６０）而计算其超速ＣＴ的钙化指数会较随机男女一起按平均计算更易区分其差异．进一步分析显示，男性中年时候超速ＣＴ指数已达最高值，而女性则晚１０年方达最高值，因此，为了更易探测冠脉循环内钙化倾向应作出超速ＣＴ检出钙化的指数数目．这些实践经验对动脉粥样硬化过程的预测或预防有实际意义．