Vol 68, No 11 (2023)

The paper presents authors’ original detailed data on rocks of the Archean Pon’goma-Navolok charnockite−enderbite complex in northern Karelia. The rocks practically have not been modified and are preserved within a rigid block among Paleoproterozoic zones of ductile deformations and metamorphism. The geochemistry of the rocks and their isotope−geochemical features indicate that the protolith from which the enderbite melts of the main phase of the massif were derived may have been amphibolites. The enderbite melts were derived from these amphibolites under the effect of K2O-, Na2O-, and SiO2-bearing fluids; and the enderbites were subsequently charnockitized with the involvement of fluids enriched in K2O and SiO2. Physicochemical modeling indicates that the enderbite melt was derived from the amphibolite protolith at a depth of about 45 km (P = 14.8 kbar, T = 1030−1080°C) under the effect of saline H2O−CO2 fluid. Comparison of the P−T parameters of the granulite-facies metamorphism of the metabasites and the parameters under which the enderbite melts were derived indicates that Archean granulite-facies metamorphism in the Belomorian belt in northern Karelia was of contact but not regional nature and was induced by the high-temperature field of an emplaced enderbite massif. The orthogneisses hosting the Pan’goma-Navolok massif inherit geochemical features of the unsheared, ungneissose, and unmetamorphosed enderbites. This means that enderbites analogous to those of the Pan’goma-Navolok massif may have served as the protolith of some of the orthogneisses, and that enderbites may have been spread more widely in the Archean than the currently preserved single enderbite massifs.

An experimental study of the main factors affecting the accuracy of oxygen and carbon isotopic analysis in carbonates dispersed in silicate matrix is carried out. Artificial 1, 2, 5, and 10% mixtures of quartz with carbonates with different isotopic parameters (KH-2, Ko, MCA-8) were analyzed by continuous flow isotope ratio mass spectrometry (CF IRMS). It is established that, in addition to the influence of the instrumental nonlinearity, the results are affected by two factors: trace amounts of CO2, constantly present in the system (the blank effect) and the presence of chemically neutral silicate particles (the matrix effect). The blank effect depends on the isotopic parameters of the sample and has very little influence on the estimated carbonate content in the rock. The matrix effect, on the contrary, strongly affects the estimated carbonate content, and produces the isotopic shift towards underestimated contents of heavy 13C and 18O isotopes. It is shown that this effect is related to the processes occurring near the CO2–acid–quartz interface, which are accompanied by kinetic fractionation of carbon and oxygen isotopes. Both effects are dependent on the amount of silicate matrix in the system and most clearly manifested during analysis of carbonate-poor rocks. When the carbonate content in the rock is about 1–2%, deviations from the true δ13C and δ18O values can reach the first ppm, while carbonate content obtained by chromatographic peak calibration can be underestimated by 20–40%.

The paper is devoted to the biogeochemical aspects of the treatment of iron-bearing groundwater, which are associated with the formation of biofouling in the pore space around wells after aeration of the aquifer and on technological equipment. Structure and activity characteristics of microbial complexes as a result of pumping groundwater from production and observation wells under changing redox conditions are presented. Scanning electron microscopy was used to study the microstructure and elemental composition of biofilm growths. It has been established that the accumulation of iron and manganese by microbial biomass occurs due to the encrustation of the surface of bacterial cells immersed in a polymer matrix represented by a constant base of three elements: Al, Si, and Ca. The survival of microbial complexes in biofouling is due to the high natural potential and ability to carry out biogeochemical processes in a wide range of oxygen concentrations (aerobic and anaerobic conditions).