Changes in Lumbriculus variegatus metabolites under hypoxic exposure to benzo(a)pyrene,chlorpyrifos and pentachlorophenol: Consequences on biotransformation

The regulation of endogenous metabolites is still not fully understood in aquatic invertebrates exposed concurrently to toxicants and hypoxia. Despite the prevalence of hypoxia in the aquatic environment, toxicity estimations seldom account for multiple stressors thereby differing from natural conditions. In this study, we examined the influence of hypoxia (<30% O₂) on contaminant uptake and the composition of intracellular metabolites in Lumbriculus variegatus exposed to benzo(a)pyrene (B(a)P, 3 μg L⁻¹), chlorpyrifos (CPF, 100 μg L⁻¹) or pentachlorophenol (PCP, 100 μg L⁻¹). Tissue extracts of worms were analyzed for 123 metabolites by gas chromatography–mass spectrometry and metabolite levels were then related to treatments and exposure time. Hypoxia markedly increased the accumulation of B(a)P and CPF, which underlines the significance of oxygen in chemical uptake. The oxygen effect on PCP uptake was less pronounced. Succinate and glycerol-3-phosphate increased significantly (p < 0.0001) following hypoxic treatment, whereas sugars, cysteine, and cholesterol were effectively repressed. The buildup of succinate coupled with the corresponding decline in intracellular 2-oxo- and 2-hydroxy glutaric acid is indicative of an active hypoxia inducible factor mechanism. Glutamate, and TCA cycle intermediates (fumarate, and malate) were disturbed and evident in their marked suppression in worms exposed concurrently to hypoxia and PCP. Clearly, hypoxia was the dominant stressor for individuals exposed to B(a)P or CPF, but to a lesser extent upon PCP treatment. And since oxygen deprivation promotes the accumulation of different toxicants, there may be consequences on species composition of metabolites in natural conditions.     

Temporal change estimation of mercury concentrations in northern pike (Esox lucius L.) in Swedish lakes

Adequate temporal trend analysis of mercury (Hg) in freshwater ecosystems is critical to evaluate if actions from the human society have affected Hg concentrations ([Hg]) in fresh water biota. This study examined temporal change in [Hg] in Northern pike (Esox lucius L.) in Swedish freshwater lakes between 1994 and 2006. To achieve this were lake-specific, multiple-linear-regression models used to estimate pike [Hg], including indicator variables representing time and fish weight and their interactions. This approach permitted estimation of the direction and magnitude of temporal changes in 25 lakes selected from the Swedish national database on Hg in freshwater biota. A significant increase was found in 36% of the studied lakes with an average increase in pike [Hg] of 3.7 ± 6.7% per year that was found to be positively correlated with total organic carbon. For lakes with a significant temporal change the dataset was based on a mean of 30 fish, while for lakes with no temporal change it was based on a mean of 13 fish.     

Quantifying Metal Contributions from Multiple Sources to the Clark Fork River,Montana, U.S.A.

Identifying and quantifying the contributions of multiple sources of trace elements to stream sediments in a basin containing several possible inputs presents a unique problem related to the investigation of rivers impacted by industrial activity. A multi-source dilution-mixing model was developed and applied to determine the relative contributions to As, Cu and Pb burdens in the Clark Fork River, Montana, a recipient of historical mine wastes as a result of over a century of mining and milling operations. The results identified the Flint Creek drainage as a major source of anthropogenic As (47%) and Pb (35%) to sediments of the Clark Fork River and the Milltown Reservoir, in addition to the major sources associated with mining operations in Butte, MT. The Little Blackfoot River also contributes anthropogenic As (3%) and Pb (4%) to the Clark Fork River, while minor inputs of Cu (1%) and Pb (2%) emanate from the Blackfoot River. The model allows source quantification, and an understanding of the fate and transport of mine wastes in a basin, allowing identification and eventual prioritization of sites destined for remediation.     

Biodegradation of PAHs in soil: Influence of chemical structure, concentration and multiple amendment

The influence of PAH chemical structure and concentration, added in either single (75 or 300 mg kg⁻¹) or multiple (2 × 75, 2 × 150 or 4 × 75 mg kg⁻¹) applications as single- or multiple-contaminant systems, on the development of PAH biodegradation in a pristine soil was investigated. Development in microbial catabolic ability was assessed at 0, 28, 56 and 84 d by monitoring ¹⁴C-naphthalene, ¹⁴C-phenanthrene and ¹⁴C-pyrene mineralisation over 14 d in respirometric assays. The presence of other contaminants influenced the ability of the indigenous microflora to mineralise structurally different contaminants over time. ¹⁴C-Naphthalene mineralisation was inhibited by the presence of other contaminants; whereas the presence of naphthalene significantly enhanced rates of mineralisation in multiple-contaminant systems containing ¹⁴C-phenanthrene and ¹⁴C-pyrene. Generally, increasing the number of contaminant applications has implications for catabolic activity of soil microbes. It is suggested the toxic nature of PAHs retarded mineralisation at increased contaminant concentrations.     

History of mercury use and environmental contamination at the Oak Ridge Y-12 Plant

Between 1950 and 1963 approximately 11 million kilograms of mercury (Hg) were used at the Oak Ridge Y-12 National Security Complex (Y-12 NSC) for lithium isotope separation processes. About 3% of the Hg was lost to the air, soil and rock under facilities, and East Fork Poplar Creek (EFPC) which originates in the plant site. Smaller amounts of Hg were used at other Oak Ridge facilities with similar results. Although the primary Hg discharges from Y-12 NSC stopped in 1963, small amounts of Hg continue to be released into the creek from point sources and diffuse contaminated soil and groundwater sources within Y-12 NSC. Mercury concentration in EFPC has decreased 85% from ∼2000 ng/L in the 1980s. In general, methylmercury concentrations in water and in fish have not declined in response to improvements in water quality and exhibit trends of increasing concentration in some cases.     

Assessing the nature of the combined effects of copper and zinc on estuarine infaunal communities

Elevated levels of copper and zinc in sediment have been shown to adversely affect estuarine infauna. We investigated the additivity of the combined effects of copper and zinc on infaunal recolonisation through a manipulative field experiment in Orewa estuary, New Zealand, using defaunated sediment discs treated with these metals. The nature of their combined effects varied among infaunal taxa and the particular variables being examined. Additive effects were detected for species richness, for the mean log abundances of the polychaetes Prionospio sp. and Scoloplos cylindrifer and for the multivariate response of the community as a whole. Antagonistic effects were detected for the mean log abundances of total infauna and the polychaete Heteromastus sp. Characterising the potentially interactive nature of the combined effects of multiple heavy metals is essential in order to build predictive models of future environmental impacts of metal accumulation in estuarine sediments.     

火灾自动探测的复合特定趋势算法

本文提出了二输入信号的复合特定趋势检测算法，它能够根据信号的稳定值识别复合信号位于稳定值上方的正向变化和稳定值下方的负向变化趋势，在趋势判断函数中引入判别门限，有效地克服了随机噪声干扰；在火灾信号确认中使用了“趋势持续”方法，通过标准试验火和不同环境下非火灾信号的模拟测试表明，该算法探测火灾信号及时、可靠且具有极低的误报警率。     

双火源条件下的XPS火蔓延速率研究

为研究挤塑聚苯乙烯泡沫板(XPS)双火源火焰迁移规律,在不同间距(0.5cm~8cm)的情况下,进行了竖直和水平方向的系列实验。研究发现:火蔓延速率和质量损失速率均随间距先上升后缓慢下降;在竖直方向实验中,火蔓延速率极值点右偏移于质量损失极值点。基于双火源条件下所得到的热解区传热系数,计算出火蔓延速率,进而分析火蔓延速率计算式中对流项和辐射项,得出火蔓延速率随间距的变化主要受控于传热系数。依据此结论解释了火蔓延速率和质量损失趋势相似但两者极值点偏移不同的原因。