geochemical indicators
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2022 ◽  
Author(s):  
Jiří Mizera ◽  
Zdeněk Řanda

ABSTRACT Formation of the Central European tektites, known as moldavites, has been associated with a large meteorite impact in southern Germany 14.8 m.y. ago. The geochemical link between moldavites and their source materials, and the processes of their possible chemical differentiation still remain uncertain. Some differences in chemical composition between moldavites and sediments of corresponding age from the surroundings of the Ries crater could be explained by a hypothesis according to which biomass covering the pre-impact area contributed to the source materials. In a comparison of the geochemical compositions of a large representative set of moldavites and suitable Ries sediments, enrichment in elements K, Ca, Mg, and Mn and depletion of Na in moldavites, similar to redistribution of these elements during their transfer from soil to plants, could indicate the unconventional biogenic component in moldavite source materials. Simple mixing calculations of the most suitable Ries sediments and a model biogenic component represented by burned biomass residue are presented. The plausibility of the estimated biomass contribution considering reconstructions of the middle Miocene paleoenvironment in the pre-impact Ries area is discussed. No significant vapor fractionation is required to explain the observed variability of moldavite chemical composition.


Author(s):  
Teng Li ◽  
Hui Gao ◽  
Chen Wang ◽  
Zhilin Cheng ◽  
Yanning Yang ◽  
...  

AbstractShale gas reservoir is a fine-grained sedimentary rock with component of clastic particles and organic matters, and the accumulation of the organic matters would determine the effective development of shale gas. The paleoclimate, detrital influx, redox of the water and paleoproductivity are effective geochemical indicators that could help to find the favorable shale gas reservoir stratum. In this study, the shale samples collected from Niutitang Formation (Northern Guizhou, China) were launched the measurements of the content of major elements and trace elements, and the characteristics of geochemical indicators were analyzed, which can be used to discuss the accumulation model of organic matters. Besides, the pore structure of shale sample controlled by the enrichment of organic matters is also discussed. The paleoclimate is dominant cold and dry, and it changes to warm and humid at the later Niutitang period, and the detrital influx also increased at the later Niutitang period; the water environment of Niutitang Formation shale presents as reductive, and the paleoproductivity of the Niutitang Formation shale is commonly high. The enrichment of organic matters in the Niutitang Formation is dominantly controlled by the redox of the water, while the hydrothermal activity and the paleoproductivity lead to the difference enrichment of organic matters in the Niutitang Formation shale. The accumulation model of organic matters also influences the characteristics of pore structure from the Niutitang Formation shale, and the pore structure could be divided into two types. The shale with high content of organic matters also features high content of quartz and pyrite, and these minerals contribute to the preservation of pore space in the shale, while that of the clay minerals is contrary. The high content of organic matters and preferable pore characteristics indicate the Niutitang Formation favors the development of shale gas, especially that for the lower Niutitang Formation.


Author(s):  
Magdalena Szara-Bąk ◽  
Agnieszka Baran ◽  
Agnieszka Klimkowicz-Pawlas ◽  
Joanna Tkaczewska ◽  
Barbara Wojtasik

AbstractThe aim of the study was to use of geochemical, chemical, ecotoxicological and biological indicators for a comprehensive assessment of ecological risks related to the mobility, ecotoxicity and bioavailability of trace elements in the bottom sediment of the Rożnów reservoir. The study found three elements deserving attention in the sediments: cadmium, nickel and chromium. Cadmium proved to be the most mobile and bioavailable, although the total cadmium content and geochemical indicators did not reveal any risk to organisms. Geochemical indicators showed that the sediments are contaminated with nickel and chromium, but both elements had a low bioaccumulation factor. Fractional analysis also revealed relatively low mobility of Cr and Ni and a higher potential risk of bioavailability for nickel. Most of the tested sediment samples had low toxicity in relation to the tested organisms. For H. incongruens, 11% of the samples were non-toxic, 50% of the samples had low toxicity, and 39% of the samples were toxic. For A. fischeri, no toxicity was found in 7% of the samples, low toxicity in 76% of the samples and toxicity in 17% of the sediment samples. The As, Cd, Cu content in the F1 fraction correlated significantly positively with the content of these metals in mussel tissues. Both biotesting and chemical analysis can reveal a potential risk to aquatic organisms. For a real assessment of the ecological risks associated with trace elements, it is necessary to use bioindicators taken from the environment and exposed to trace elements in situ.


Author(s):  
M.Yu. Chudetsky

The paper analyzes the sources of occurrence in oil reservoirs of biomarkers related to tetracyclic and pentacyclic isoprenoids. These molecules are widely known and traditionally used as indicators of oil maturity; however, the concept of organisms that produce these molecules remains controversial. A look at these biomarkers in the light of modern advances in microbiology indicates that some of these molecules were synthesized by microorganisms of the underground biosphere directly in the deposits. This interpretation invites us to rethink and re-evaluate geochemical indicators that are considered non-informative and often ignored.


Author(s):  
Matthew J Valetich ◽  
Charles Le Losq ◽  
Richard J Arculus ◽  
Susumu Umino ◽  
John Mavrogenes

Abstract Much of the boninite magmatism in the Izu-Bonin-Mariana (IBM) arc is preserved as evolved boninite series compositions wherein extensive fractional crystallisation of pyroxene and spinel have obscured the diagnostic geochemical indicators of boninite parentage, such as high-Mg and low-Ti at intermediate silica contents. As a result, the usual geochemical discriminants used for the classification of the broad range of parental boninites are inapplicable to such highly fractionated melts. These issues are compounded by the mixing of demonstrably different whole-rock and glass analyses in classification schemes and petrological interpretations based thereon. Whole-rock compositions are compromised by entrainment of variable proportions of crystalline phases resulting in inconsistent differences with corresponding in-situ glass analyses, which arguably better reflect prior melt compositions. To circumvent such issues, we herein present a robust method for the classification of highly fractionated boninite series glasses. This new classification leverages the analysis of trace elements, much more sensitive to evolutionary processes than major elements, and benefits from the use of unsupervised machine learning as a classification tool. The results show the most fractionated boninite series melts preserve geochemical indicators of their parentage, and highlight the pitfalls of interpreting whole rock and glass analyses interchangeably.


2020 ◽  
pp. 22-31
Author(s):  
S. A. Milyaev ◽  
G. G. Samosorov ◽  
S. V. Yablokova ◽  
L. V. Shatilova ◽  
N. N. Pozdnyakova

The features of impurity element distribution in native gold of two ore formation gold deposit types are con- sidered. A typomorphic set of elements for gold-polysulfide-quartz and gold-quartz low-sulfide mineralization was determined. Geochemical indicators for estimating ore formation types of native gold are offered. The differences in gold composition due to metallogenic specialization of regions are established. Data on the distribution of rare-earth elements in native gold are obtained, which allows to predict igneous rocks composition during gold-polysulfide-quartz deposit formation.


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