Abstract 3,5,6-trichloropyridinol (TCPY) is a metabolite of chlorpyrifos and chlorpyrifos-methyl, whose presence in the environment is of potential toxicity to human. So, it is need to monitor and regualte TCPY levels to protect human health. However, it is not known whether TCPY is associated with all-cause and cancer mortality and to which degree its levels contributed to hazard risk. The study enrolled 3951 participants from the National Health and Nutrition Examination Surveys (NHANES). Ultra-high performance liquid chromatography coupled with electrospray ionization tandem mass spectrometry was used to measure urinary TCPY. Cox proportional hazards regression analysis was performed to explore the associations between TCPY and all-cause and cancer mortality. The study found that the average level of TCPY in the cohort was 1.79 μg/L and was higher in those who had passed away. Individuals in the highest quartile had a 1.56-fold independent increase in rate for all-cause mortality compared to those in the lowest quartile (hazard ratio [HR] 1.56, 95% confidence interval 1.09–2.24, p = 0.002). However, while the univariate model showed a hazard ratio of 2.37 (1.19–4.71) for the highest quartile in regards to cancer mortality, this association disappeared after adjusting for demographics, lifestyles, and comorbidities. Exposure to urinary 3,5,6-trichloropyridinol, as a result of insecticide exposure, increased the rate of all-cause mortality but was not independently associated with cancer mortality.
Forests can accumulate large quantities of SOC, but the trend in SOC accumulation with increasing stand age is inconclusive. In this study, we selected five plots in northwestern China: four stands of artificially planted Robinia pseudoacacia of different ages (5, 20, 40, and 56 years old), and a plot of wasteland as the control. The results showed that the SOC contents decreased, whereas δ13C values increased, with soil depth. The soil total nitrogen (TN) content and the carbon/phosphorus (C/P) ratio increased significantly with increasing stand age. The SOC storage in the 0–30 cm soil layer did not differ significantly among stands of different ages. However, SOC storage in the 0–100 and 30–100 cm soil layers was significantly higher in the 40- and 56-year-old stands than in 5-year-old stands. The SOC turnover rate decreased gradually over the 40 years after planting and then rapidly increased between 40 and 56 years after planting. The SOC stocks were most strongly correlated with TN and the C/P ratio, and SOC turnover was most closely related to soil porosity. Afforestation significantly improved soil properties to enhance SOC sequestration, but it took a long time for stored SOC to accumulate in this study area.
Abstract Microbial moribunds after microbial biomass turnover (microbial residues) contribute to the formation and stabilization of soil carbon pools; however, the factors influencing their accumulation on a global scale remain unclear. Here, we synthesized data for 268 amino sugar concentrations (biomarkers of microbial residues) in grassland and forest ecosystems for meta-analysis. We found that soil organic carbon, soil carbon-to-nitrogen ratio, and aridity index were key factors that predicted microbial residual carbon accumulation. Threshold aridity index and soil carbon-to-nitrogen ratios were identified (~0.768 and ~9.583, respectively), above which microbial residues decreased sharply. The aridity index threshold was associated with the humid climate range. We suggest that the soil carbon-to-nitrogen ratio threshold may coincide with a sharp decrease in fungal abundance. Although dominant factors vary between ecosystem and climate zone, with soil organic carbon and aridity index being important throughout, our findings suggest that climate and soil environment may govern microbial residue accumulation.
The “dolomite problem”, which has confused scientists for nearly two centuries, is an important fundamental geological problem. The mineralogical characteristics of carbonate minerals show that the dolomite structure consists of an ordered arrangement of alternating layers of Ca2+ and Mg2+ cations interspersed with CO32− anion layers normal to the c-axis. The dolomite structure violates the c glide plane in the calcite structure, which means that dolomite has R3¯ space group symmetry. The ordered dolomite has superlattice XRD reflections [e.g., (101), (015) and (021)], which distinguish it from calcite and high-Mg calcite. The calculation of thermodynamic parameters shows that modern seawater has a thermodynamic tendency of dolomite precipitation and the dolomitization reaction can be carried out in standard state. However, the latest thermodynamic study shows that modern seawater is not conducive to dolomitization, and that seawater is favorable for dolomitization in only a few regions, such as Abu Dhabi, the Mediterranean and the hypersaline lagoons in Brazil. The kinetic factors of dolomite formation mainly consist of the hydration of Mg2+, the presence of sulfate and the activity of carbonate. Current studies have shown that the presence of microorganisms, exopolymeric substances (EPS), organic molecules, carboxyl and hydroxyl functional groups associated with microorganisms and organic molecules, clay minerals with negative charges and dissolved silica facilitate magnesium ions to overcome hydration and thus promote Mg2+ incorporation into growing Ca-Mg carbonates. Similarly, the metabolic activity of microorganisms is conducive to the increase in alkalinity. However, the inhibitory effect of sulfate on dolomite formation seems to be overestimated, and sulfate may even be a catalyst for dolomite formation. Combining the carbonate crystallization mechanism with thermodynamic and kinetic factors suggests that the early stage of dolomite precipitation or the dolomitization reaction may be controlled by kinetics and dominated by unstable intermediate phases, while metastable intermediate phases later transform to ordered dolomite via an Ostwald’s step rule.