Urinary concentrations of organophosphorus insecticide metabolites in Japanese workers

A recent development in analytical chemistry has enabled us to monitor systemic organophosphorus insecticide (OP) exposure at individual levels. At present, however, limited data are currently available on urinary OP metabolite levels worldwide. The purpose of this study was to assess urinary dialkylphosphate (DAP) concentrations in Japanese workers. Urine samples were collected in both summer and winter from 339 Japanese adults who worked as food distributors (FDs, n = 164), apple farmers (AFs, n = 147) and pest control operators (PCOs, n = 28). DAPs were measured by gas chromatography-mass spectrometry after derivatization with pentafluorobenzylbromide. Dimethylphosphate (DMP), diethylphosphate (DEP), dimethylthiophosphate (DMTP) and diethylthiophosphate (DETP) were detected in the urine of over 87% of the studied populations in both seasons. The geometric mean values of total DAPs (nmol g⁻¹ creatinine), DMP, DMTP, DEP and DETP (μg g⁻¹ creatinine) in summer and winter were 106.7 and 98.3, 7.0 and 3.8, 3.4 and 4.5, 0.8 and 1.5, and 0.3 and 0.2 for the FDs, 440.8 and 197.7, 33.1 and 10.8, 10.1 and 5.8, 4.2 and 4.7 and 1.6 and 0.8 for the AFs, and 473.4 and 284.6, 28.9 and 22.2, 17.6 and 4.6, 3.5 and 4.4, and 0.5 and 0.6 for the PCOs, respectively, thereby revealing significantly higher concentrations in AFs and PCOs groups than in the FDs in both seasons except for winter DMTP. These DAP concentrations were approximately the same or at lower levels compared with those reported in the previous literature. This is one of the first studies to demonstrate urinary DAP concentrations in Japanese adults.     

The sensitivity of carbon sequestration to harvesting and climate conditions in a temperate cypress forest: Observations and modeling

The role of disturbance and climate factors in determining the forest carbon balance was investigated at a Japanese cypress forest in central Japan with eddy flux measurements, tree-ring analyses, and a terrestrial biosphere model. The forest was established as a plantation after intermittent harvesting and replanting between 1959 and 1977, and acted as a strong carbon sink of approximately 500 g C m⁻² year⁻¹ for the measurement years between 2001 and 2007. A terrestrial biosphere model, BIOME-BGC, was validated using the eddy flux data at daily to interannual timescales, and the tree-ring width data at interannual to decadal timescales. According to the model simulation, during the observation period 270 ± 55 g C m⁻² year⁻¹ was additionally sequestered due to the indirect effects of the harvesting and planting, whereas the increase of CO₂ concentration and the change in climate increased the sink of 110 ± 40 and 30 ± 80 g C m⁻² year⁻¹, respectively. The model simulation shows that the forest is now recovering from harvesting, and that harvesting is a more important determinant of the current carbon sink than either interannual climate anomalies or increased atmospheric CO₂ concentration. We found that harvesting with long rotation length could be effective management activity in order to increase carbon sequestration, if the harvested timber is converted into products with long lifecycles.     

Application of crosswell seismic tomography using difference analysis with data normalization to monitor CO2 flooding in an aquifer

A pilot-scale experiment for carbon dioxide (CO₂) sequestration was undertaken at the Nagaoka test field in Japan. Time-lapse crosswell seismic tomography was conducted to detect and monitor the movement of CO₂ injected into an aquifer. We applied difference analysis with data normalization (DADN) to the time-lapse data to eliminate false images that were apparent in a conventionally processed difference section. Conventional difference analysis calculates travel-time delays after inversion, whereas the DADN method calculates them from raw travel-time records before inversion. Thus, fewer errors are generated with the DADN method compared to a conventional inversion analysis. We applied the DADN method to time-lapse tomography data recorded before and after the injection of CO₂ and computed the velocity variation in a subsurface section, which clearly showed the distribution of CO₂ flooding within a high permeability zone in the aquifer and showed no CO₂ leakage into the caprock. Our results also show the maximum velocity decrease as a result of CO₂ injection was about 9%, which is close to the results obtained in laboratory experiments. Finally, numerical simulations were inverted to test the effectiveness of the conventional and DADN methods in dealing with noise. These tests showed that the DADN method effectively reduces unique coherent noise for particular receiver and source combinations. We concluded that the DADN method provides useful data for monitoring the flow of CO₂ sequestered in underground aquifers.     

Ethyl mercury induces Ca2+ uptake through the P2×7 receptor in a mouse cerebellar microglia cell line

Many observations are reported that organic mercury compounds are involved in increasing intracellular Ca²⁺ levels. However, the issue of which substances on the cell membrane participate in the Ca²⁺ uptake that is induced by ethyl mercury is unclear. The findings of this study suggest that the P2X receptor participates in this process. The uptake of Ca²⁺ by C8-B4 cells was induced in the presence of ethyl mercury. Ca channels in the cell membrane were not affected in this process. In contrast, pretreatment with suramin, an antagonist of the P2X receptor, inhibited the Ca²⁺ uptake induced by ethyl mercury, and also brilliant blue G, a nonselective antagonist of P2×4, P2×5, and P2×7 receptors. In addition, A438079 and A740003, selective antagonists of P2×7 receptor, reduced Ca²⁺ uptake, while 5-BDBD, a selective antagonist of P2×4 receptor, did not. Furthermore, the mRNAs of both the P2×4 and P2×7 receptors were expressed in the presence of ethyl mercury, but the P2×5 receptor mRNA was not. These findings suggest that ethyl mercury may induce Ca²⁺ uptake through the P2×7 receptor of the cell membrane.