The Vuoriyarvi Devonian carbonatite–ijolite–pyroxenite–olivinite complex comprises several carbonatite fields: Neske Vara, Tukhta-Vara, and Petyayan-Vara. The most common carbonatites in the Tukhta-Vara and Neske-Vara fields are calciocarbonatites, which host several P, Fe, Nb, and Ta deposits. This paper focuses on the Petyayan-Vara field, in which the primary magmatic carbonatites are magnesian. The least altered magnesiocarbonatites are composed of dolomite with burbankite and are rich in REE (up to 2.0 wt. %), Sr (up to 1.2 wt. %), and Ba (up to 0.8 wt. %). These carbonatites underwent several stages of metasomatism. Each metasomatic event produced a new rock type with specific mineralization. The introduction of K, Si, Al, Fe, Ti, and Nb by a F-rich fluid (or fluid-saturated melt) resulted in the formation of high-Ti magnesiocarbonatites and silicocarbonatites, composed of dolomite, microcline, Ti-rich phlogopite, and Fe–Ti oxides. Alteration by a phosphate–fluoride fluid caused the crystallization of apatite in the carbonatites. A sulfate-rich Ba–Sr–rare-earth elements (REE) fluid (probably brine-melt) promoted the massive precipitation of ancylite and baryte and, to a lesser extent, strontianite, bastnäsite, and synchysite. Varieties of carbonatite that contain the highest concentrations of REE are ancylite-dominant. The influence of sulfate-rich Ba-Sr-REE fluid on the apatite-bearing rocks resulted in the dissolution and reprecipitation of apatite in situ. The newly formed apatite generation is rich in HREE, Sr, and S. During late-stage transformations, breccias of magnesiocarbonatites with quartz-bastnäsite matrixes were formed. Simultaneously, strontianite, quartz, calcite, monazite, HREE-rich thorite, and Fe-hydroxides were deposited. Breccias with quartz-bastnäsite matrix are poorer in REE (up to 4.5 wt. % total REE) than the ancylite-dominant rocks (up to 11 wt. % total REE).

The NE Fennoscandian Shield comprises the Northern Belt in Finland and the Southern Belt in Karelia. They host mafic-ultramafic layered Cu-Ni-Cr and Pt-Pd-bearing intrusions. Precise U-Pb and Sm-Nd analyses indicate the 130-Ma evolution of these intrusions, with major events at 2.53, 2.50, 2.45, and 2.40 Ga. Barren phases were dated at 2.53 Ga for orthopyroxenites and olivine gabbro in the Fedorovo-Pansky massif. PGE-bearing phases of gabbronorites (Pechenga, Fedorovo-Pansky, Monchetundra massifs) and norites (Monchepluton) are 2.50 Ga old. Anorthosites of Mt. Generalskaya (Pechenga), the Fedorovo-Pansky, and Monchetundra massifs occurred at 2.45 Ga. This event produced layered PGE-bearing intrusions in Finland (Penikat, Kemi, Koitelainen) and mafic intrusions in Karelia. The Imandra lopolith dikes occurred at the final phase (2.40 Ga). Slightly negative εNd and ISr values (0.703–0.704) suggest that intrusions originated from an enriched mantle reservoir. Low 3He/4He ratios in accessory minerals (ilmenite and magnetite) indicate an upper mantle source. Large-scale correlations link the Fennoscandian Shield with the Superior and Wyoming cratons.

The current laboratory adsorption study aimed at determination of the values of adsorption distribution coefficient (Kd) of bentazone in the profiles of Arenosols, Luvisols, and Cambisols, which are the most common arable mineral soils in Poland. The study attempted to identify the soil components that bind bentazone and the principal adsorption mechanisms of this compound as well as create a model capable of predicting its adsorption in soils. The Kd values determined in batch experiments after 24 h of shaking were very low, and ranged from 0.05 to 0.30 mL/g for the Ap horizon and 0 to 0.07 mL/g for subsoils. The results indicated that the anionic form of bentazone was adsorbed on organic matter, while in acidic soils the neutral form of bentazone was adsorbed on organic matter and sand. The detailed analyses of mineralogical composition revealed that the principal mineral that was responsible for the adsorption of bentazone was quartz, which content was strongly positively correlated with the sand fraction. In soils with pH < 5 and an organic carbon content of < 0.35%, quartz exhibited much greater affinity for the neutral bentazone form than organic matter. Fourier transform infrared photoacoustic spectroscopy analyses supported by computational methods have shown the most probable mechanisms behind the adsorption of bentazone on quartz. The created model, assuming the adsorption of bentazone on organic matter and on sand and using the spectrophotometrically determined dissociation constant of bentazone, very well explained the Kd variance in the 81 examined soils, while correctly predicting the adsorption based on soil properties described in the published data.

Thirty-eight samples of minerals from Paleoproterozoic Layered PGE Intrusion Monchepluton, located in NE Fennoscandia, were tested. An automated computational technique was used which involved counting the sides superimposed on vectorized graphics using separated crystal boundaries. The results were obtained for olivine, orthopyroxene, clinopyroxene, and plagioclase. On this basis, an interpretation of the mineral box fractal dimension was made, along with an interpretation of its nature in the rock in which it was found. The performed calculations were applied to the sampling positions, and maps of changes in fractal dimensions were prepared. The nature of the minerals studied was correlated with the type of rocks present in Monchepluton. Then, the fractal dimensions were scaled to a percentage scale determining the mean value for the euhedral crystal as 100%, and a map was obtained representing the advancement of secondary processes after summing these data for all four investigated minerals. This method was analyzed and its advantages and limitations shown.

No abstract