The fate of anthropogenic Pb in soils; years after Pb terminated as a fuel additive; Northern Israel.

The source for Lead (Pb) pollution in soils from the heavily industrialized area located along the coast of the Eastern Mediterranean, Haifa Bay, Northern Israel, is studied using the lead isotopic composition. The uniqueness of the studied data set is that it includes samples of soils, road-wash, and storm-dust sampled for nearly three decades (1988-2017). Road-wash sediments are similar in both elemental and Pb isotopic composition to soils sampled in the same year (2010), indicating re-suspension of local soil, as its origin. Soils sampled during and before 1993 show no evidence for Pb contamination (bulk soil values), although Pb as an additive was already in use. Furthermore, soil overturns hinder the possibility to trace changes in the Pb isotopic composition with time in soils of the same location. Soils sampled from 1995-8 to 2013 were significantly dominated by Post-1992 Pb additive, pointing to Pb's peak as an additive. Soils Pb and Zn Enrichment factors for most samples are below 5, and their anthropogenic source is likely common. Forest fire enriched Pb and Zn in the soil, and their Pb isotope compositions reflect this enrichment. Lead from the Hod Assaf recycling plant detected up to some 2.5 km away, and although not analyzed in the current study, dioxin-like compounds possibly accompanied Pb.

Is mercury in Tibetan Medicine toxic? Clinical, neurocognitive and biochemical results of an initial cross-sectional study.

Mercury an important therapeutic substance in Tibetan Medicine undergoes complex "detoxification" prior to inclusion in multi-ingredient formulas. In an initial cross-sectional study, patients taking Tibetan Medicine for various conditions were evaluated for mercury toxicity. Two groups were identified: Group 1, patients taking " Tsothel" the most important detoxified mercury preparation and Group 2, patients taking other mercury preparations or mercury free Tibetan Medicine. Atomic fluorescence spectrometry of Tibetan Medicine showed mercury consumption 130 µg/kg/day (Group 1) and 30 µg/kg/day (Group 2) ( P ≤ 0.001), levels above EPA (RfDs) suggested threshold (0.3 µg/kg /day) for oral chronic exposure. Mean duration of Tibetan Medicine treatment was 9 ± 17 months (range 3-116) (Group 1) and 5 ± 1.96 months (range 1-114) (Group 2) (NS) with cumulative days of mercury containing Tibetan Medicine, 764 days ± 1214 (range 135-7330) vs. 103 days ± 111 (range 0-426), respectively ( P ≤ 0.001). Comparison of treatment groups with healthy referents (Group 3) not taking Tibetan Medicine showed no significant differences in prevalence of 23 non-specific symptoms of mercury toxicity, abnormal neurological, cardiovascular and dental findings and no correlation with mercury exposure variables; consumption, cumulative treatment days, blood/ urine Hg. Liver and renal function tests in treatment groups were not significantly increased compared to referents, with mean urine Beta2 Microglobulin within the normal range and not significantly associated with Hg exposure variables after correcting for confounding variables. Neurocognitive testing showed no significant intergroup differences for Wechsler Memory Scale, Grooved Pegboard, Visual Retention, but Group1 scores were better for Mini-Mental, Brief Word Learning, Verbal Fluency after correcting for confounding variables. These results suggest mercury containing Tibetan Medicine does not have appreciable adverse effects and may exert a possible beneficial effect on neurocognitive function. Since evidence of mercury as a toxic heavy metal, however, is well known, further analysis of literature on mercury use in other Asian traditional systems is highly suggested prior to further studies.

Trace elements in striped dolphins (Stenella coeruleoalba) from the Eastern Mediterranean: A 10-years perspective.

Concentrations of Hg, Se, Cd, Cu, Zn, Fe, Mn and As, in kidney, liver, muscle and blubber from 7 specimens of Stenella coeruleoalba, stranded along the Israeli Mediterranean coast (IMC) from 2006 to 2011 (2011-series) were determined and compared to previous data on S. coeruleoalba from the IMC (2001-series). No differences were observed in essential and toxic elements concentrations, between the two series, except for hepatic Mn which was higher in the latter. Hg/Se molar ratios in blubber, kidney and liver increased linearly with log Hg concentrations, while muscle was more heterogenic in this respect. Means (±SD) of hepatic Hg concentrations (134±89 and 181±200mgkg(-1), from the 2011 and 2001 series, respectively) were similar to that found in 2007-2009 specimens from Spain, possibly reflecting the relatively high natural background levels of mercury in the Mediterranean Sea.

Tracing natural and anthropogenic Pb in sediments along the Mediterranean Coast of Israel using Pb isotopes.

The natural and anthropogenic sources of Pb in surface sediments offshore the Israeli Mediterranean coast were studied using the isotopic composition of Pb in diluted acid sediment extracts. Surface sediments were collected at the lower reaches of coastal streams, along a south-north offshore transect and at selected monitoring stations of the Dan Region Wastewater Plant (DRWP) outfall pipe. The background values of the Pb isotopic composition were determined from the deepest part of two representative cores collected offshore and were found to have a narrow range dominated mainly by clays derived from both inland soils and the Nilotic cell and to a lesser extent from the Saharan dust. The impact of the DRWP activated sludge can be traced to a distance of ca. 2 km from the outfall pipe. Enrichment factors of Zn, Cu, and Pb were up to 25 and are strongly correlated with each other and with the Pb isotopic composition, thus demonstrating the sludge to be their common source. The isotopic compositions of Pb in stream sediments have the widest range of values and indicate a strong anthropogenic contribution, probably from both post-1992 aerosols and point sources. However the impact of stream sediments on marine sediments could not be clearly detected.