Long-term effects of crude oil on microbial processes in subarctic marine sediments: Studies on sediments amended with organic nutrients

Subarctic marine sediments amended with various organic compounds were exposed to fresh Cook Inlet crude oil at a concentration of 50 ppt for either 6 or 8 months. After the sediments were initially treated, they were returned to the approximate location where they were collected and left to be exposed to natural environmental conditions until they were retrieved for analysis. As a result of crude oil treatment, the activities of the enzymes that hydrolyse structural polysaccharides were reduced and the activities of the enzymes that hydrolyse storage polysaccharides were stimulated. In addition to these changes, we observed changes in phosphatase activity, nitrogen fixation rates, potential denitrification rates, methane concentrations, CO₂ production rates, and the glucose uptake and mineralization rates. The effect of the crude oil perturbation was different depending on the organic compound used in the amended sediments. Many of these differences could be explained by the effect of crude oil on the hydrolases which were responsible for degrading the compound in question. The results of this study suggest the effect of crude oil on microbial processes may be affected by the type of organic material present in the impacted marine sediment. This study also illustrates the value of measuring hydrolase activity in studies designed to determine the effects of this or any other pollutant on microbial processes in marine sediments.     

Regional and interannual variability in sea level over 2002–2009 based on satellite altimetry, Argo float data and GRACE ocean mass

In this study, we have estimated the different sea level components (observed sea level from satellite altimetry, steric sea level from in situ hydrography—including Argo profiling floats, and ocean mass from Gravity Recovery and Climate Experiment; GRACE), in terms of regional and interannual variability, over 2002–2009. We compute the steric sea level using different temperature (and salinity) data sets processed by different groups (SCRIPPS, CLS, IPRC, and NOAA) and first focus on the regional variability in steric and altimetry-based sea level. In addition to El Nino–La Nina signatures, the observed and steric sea level data show clear impact of three successive Indian Ocean Dipoles in 2006, 2007, and 2008 in the Indian Ocean. We next study the spatial trend patterns in ocean mass signal by comparing GRACE observations over the oceans with observed minus steric sea level. While in some regions, reasonably good agreement is observed, discrepancy is noticed in some others due to still large regional trend errors in Argo and GRACE data, as well as to a possible (unknown) deep ocean contribution. In terms of global mean, interannual variability in altimetry-based minus steric sea level and GRACE-based ocean mass appear significantly correlated. However, large differences are reported when short-term trends are estimated (using both GRACE and Argo data). This prevents us to draw any clear conclusion on the sea level budget over the recent years from the comparison between altimetry-based, steric sea level, and GRACE-based ocean mass trends, nor does it not allow us to constrain the Glacial Isostatic Adjustment correction to apply to GRACE-based ocean mass term using this observational approach.     

Natural Attenuation of Perchlorate in Denitrified Groundwater

Monitoring of a well‐defined septic system groundwater plume and groundwater discharging to two urban streams located in southern Ontario, Canada, provided evidence of natural attenuation of background low level (ng/L) perchlorate (ClO₄^?) under denitrifying conditions in the field. The septic system site at Long Point contains ClO₄^? from a mix of waste water, atmospheric deposition, and periodic use of fireworks, while the nitrate plume indicates active denitrification. Plume nitrate (NO₃^?‐N) concentrations of up to 103 mg/L declined with depth and downgradient of the tile bed due to denitrification and anammox activity, and the plume was almost completely denitrified beyond 35 m from the tile bed. The ClO₄^? natural attenuation occurs at the site only when NO₃^?‐N concentrations are <0.3 mg/L, after which ClO₄^? concentrations decline abruptly from 187 ± 202 to 11 ± 15 ng/L. A similar pattern between NO₃^?‐N and ClO₄^? was found in groundwater discharging to the two urban streams. These findings suggest that natural attenuation (i.e., biodegradation) of ClO₄^? may be commonplace in denitrified aquifers with appropriate electron donors present, and thus, should be considered as a remediation option for ClO₄^? contaminated groundwater.     

临界转换的早期预警信号

从生态系统到金融市场和气候在内的很多复杂动力系统,都会有临界点,在这样的点上系统可能会发生突变,从而演变到一个对立的动力模式上。在这样的临界点到达之前对其进行预测极为困难,但是现在,不同科学领域的研究工作表明,普遍性的早期预警信号有迹可循。对一系列不同类型的系统来说,这些信号会指示是否正在趋近一个临界阈值。     

Pore Water Characteristics Following a Release of Neat Ethanol onto Pre-existing NAPL

Neat ethanol (75.7 L) was released into the upper capillary zone in a continuous-flow, sand-packed aquifer tank (8.2 m³) with an average seepage velocity of 0.75 m/day. This model aquifer system contained a residual nonaqueous phase liquid (NAPL) that extended from the capillary zone to 10 cm below the water table. Maximum aqueous concentrations of ethanol were 20% v/v in the capillary zone and 0.08% in the saturated zone at 25 and 30 cm downgradient from the emplaced NAPL source, respectively. A bench-scale release experiment was also conducted for a similar size spill (scaled to the plan area). The concentrations of ethanol in ground water for both the bench- and pilot-scale experiments were consistent with advective–dispersive limited mass transfer from the capillary to the saturated zone. Concentrations of monoaromatic hydrocarbons and isooctane increased in the pore water of the capillary zone as a result of both redistribution of residual NAPL (confirmed by visualization) and enhanced hydrocarbon dissolution due to the cosolvent effect exerted by ethanol. In the tank experiment, higher hydrocarbon concentrations in ground water were also attributed to decreased hydrocarbon biodegradation activity caused by preferential microbial utilization of ethanol and the resulting depletion of oxygen. These results infer that spills of highly concentrated ethanol will be largely confined to the capillary zone due to its buoyancy, and ethanol concentrations in near-source zone ground water will be controlled by mass transfer limitations and hydrologic conditions. Furthermore, highly concentrated ethanol releases onto pre-existing NAPL will likely exacerbate impacts to ground water, due to NAPL mobilization and dissolution, and decreased bioattenuation of hydrocarbons.     

Soluble iron sulfide species in natural waters: Reappraisal of their stoichiometry and stability constants

A wide range of stoichiometries has been previously proposed for soluble iron sulfide species and there is no general agreement on their importance in natural waters. The solubility of Fe(II) in 0.1 M NaClO₄ equilibrated at 20 - 0.1°C with various partial pressures of H₂S (0.1, 0.001, 0.0001, 0.00001 MPa) was measured in the pH range 3.1-7.9. Equilibrium was established within 1-6 h when amorphous FeS was the solid phase. The results could all be fitted using values for the solubility product constant (I = 0) of p*K_s = 3.00 - 0.12 and of the stability constant for a soluble Fe(HS) ₂ species (I = 0) of p#₂ = -6.45 - 0.12 where *K_s = aFe²⁺ · aHS-/aH⁺ and #₂ = aFe(HS) ₂/aFe²⁺ · (aHS^-)². Any soluble species of the form Fe_x (HS) _2x where x = &gif1; would fit the data equally well. Measurements at different partial pressures are inconsistent with labile species of the form Fe_xS_x. There was no evidence for a Fe(HS) ⁺ species. When a solution is saturated with respect to amorphous FeS, Fe(HS) ₂ will only be a significant proportion of Fe(II) when S(-II) is higher than 0.2mmoll^-1. The constants for Fe(HS) ₂ or Fe_x (HS) _2x (x S 2) are consistent with all freshwater data where constant values of measured ion activity products provide no evidence for soluble complex formation. For marine waters with high sulfide concentrations (S 6mmol l^-1), measured concentrations of Fe(II) are consistent with there being negligible soluble iron sulfide. The data are better fitted if the dissolved species are polymeric as predicted concentrations of the monomer Fe(HS) ₂ are significant. These findings suggest that rather than the dissolved species being Fe(HS) ₂, it is probably polymeric, that is Fe_x (HS) _2x (x S 2).     

Sediment deposition from flow at low gradients into a buffer strip—a critical test of re-entrainment theory

The spatial and size distribution of sediment deposited from short periods of overland flow due to the effect of a simulated grass buffer strip was measured for low slopes of 1.6, 3.4 and 5.1%. These data were analysed so as to critically evaluate two alternative models of the process of re-entrainment of recently deposited sediment. A model of re-entrainment, previously thought to be appropriate only for a steady-state or equilibrium situation, was found to give better agreement with experiments than did a model previously used in the literature on this subject.