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The environmental assessment and identification of sources of heavy metals in Zn-Pb ore deposits are important steps for the effective prevention of subsequent contamination and for the development of corrective measures. The concentrations of eight heavy metals (As, Cd, Cr, Cu, Hg, Ni, Pb, and Zn) in soils from 40 sampling points around the Jinding Zn-Pb mine in Yunnan, China, were analyzed. An environmental quality assessment of the obtained data was performed using five different contamination and pollution indexes. Statistical analyses were performed to identify the relations among the heavy metals and the pH in soils and possible sources of pollution. The concentrations of As, Cd, Pb, and Zn were extremely high, and 23, 95, 25, and 35% of the samples, respectively, exceeded the heavy metal limits set in the Chinese Environmental Quality Standard for Soils (GB15618-1995, grade III). According to the contamination and pollution indexes, environmental risks in the area are high or extremely high. The highest risk is represented by Cd contamination, the median concentration of which exceeds the GB15618-1995 limit. Based on the combination of statistical analyses and geostatistical mapping, we identified three groups of heavy metals that originate from different sources. The main sources of As, Cd, Pb, Zn, and Cu are mining activities, airborne particulates from smelters, and the weathering of tailings. The main sources of Hg are dust fallout and gaseous emissions from smelters and tailing dams. Cr and Ni originate from lithogenic sources.

Agricultural soils from Dongchuan copper mining area were sampled and analyzed to determine the concentrations of selected trace elements, namely As, Cd, Cr, Cu, Hg, Ni, Pb and Zn. The main objectives of this study were: (1) To determine the levels of trace elements and their spatial distribution in soils; (2) to evaluate the potential ecological risk; and (3) to identify the main sources of risk element pollution. The environmental risks were assessed using five different contamination and pollution indexes. Descriptive and exploratory statistical analyses were performed to identify the relations among the trace elements in soils and possible sources of pollution. Although the values of As, Cu and Zn in the soils were significantly higher than Yunnan background values and exceeded the limits of the Chinese national standards in several sampling points, the most serious threat for the ecosystem and human health was represented by Cd. The main sources of Cu and As were identified mining activities, airborne particulates from smelters and the weathering of tailings, and partly also agricultural fertilizers. The major source of Cd was agricultural fertilizers and partly sources associated with mining and smelting activities.

The Cenozoic Xihu Sag in the East China Sea Shelf Basin contains large reserves of coals together with liquid petroleum derived from coal‐associated sediments. However, the origin of the petroleum is not well understood. In this study, biomarker assemblages in a suite of recently discovered light oils and condensates from the Paleogene succession in the western margin of in the Xihu Sag were investigated using gas chromatography – mass spectrometry. The objectives were to investigate the samples' thermal maturity and the depositional environment of the precursor source rocks which generated the oils. The light oils are believed to have been derived from coaly source rocks in the Eocene Pinghu Formation. Assessment of thermal maturity based on CPI, pristane/n‐C17 ratio and isomerisation ratios of C29 steranes and C31 homohopanes suggest that the hydrocarbons have a relatively low maturity in the early to mid oil generation window. The distribution of isoprenoids relative to n‐alkanes, the high pristane/phytane ratios (5.1–10.7), the almost complete absence of gammacerane and C33+ homohopanes, and the low dibenzothiophene/phenanthrene ratios indicate that the source rocks of the hydrocarbons were deposited in a relatively oxic and sulphate‐poor fluvio‐deltaic environment which was favourable for coal measure development. Abnormally abundant gymnosperm‐derived diterpanes including labdane, 19‐norisopimarane, fichtelite, rimuane, pimarane, isopimarane, 17‐nortetracyclic diterpene, phyllocladanes and abietane were detected in the samples analysed. 16a(H)‐Phyllocladane was identified unambiguously and kauranes were confirmed to be absent. In addition, three 19‐norisopimarane isomers, 13β(H)‐atisane, and 20‐normethylatisane were tentatively identified in the studied samples. The distributions of n‐alkanes, isoprenoids and regular steranes, the presence of 4β(H)‐eudesmane and oleanane, high Pr/Ph ratios and the abundant diterpanes together suggest that the hydrocarbons were derived from a coaly source rock. Gymnosperms of the conifer families Cupressaceae (especially the former Taxodiaceae) and Pinaceae are interpreted to be the major source of the diterpanes and to have made a significant contribution to the coaly source rock. However, the low abundance of oleanane relative to diterpanes may underestimate the contribution from angiosperms relative to gymnosperms. This could be due to differential preservation and alteration of the di‐ and triterpenoid precursors during diagenesis and the occurrence of non‐specific precursors in higher land plants.