R. Tyszka, A. Pietranik, Beata Marciniak-Maliszewska, Jakub Kierczak
Heavy mineral particles are widely used in Earth science studies to show sediment provenance and weathering conditions. Such particles are particularly useful in polluted soils surrounding mining and smelting facilities because heavy minerals are common by-products of these activities and may accumulate in the soils. As such, the particles are suitable indicators of metallic element carriers and their stability in the soil environment. In this study, we analyze heavy mineral particles in two soils surrounding the active copper smelter (Legnica, SW, Poland). We show that particles associated with different smelting activities dominate the heavy mineral fraction. We note the general absence of sulfides in the fraction indicating that these minerals might have been entirely dissolved, but timing of this dissolution is uncertain (before or after deposition within soils). Currently, the carriers of potentially toxic elements are mainly secondary Fe oxides. Studies aiming at better estimation of the proportion of metallic elements contained in heavy mineral particles are needed to fully use the potential of these phases in polluted soil studies. We estimate that Pb contained in Pb-rich silicate glass constitutes <0.5% of the total Pb budget and Pb contained in secondary Fe oxides is over 1% of the total budget, but these are minimal estimates.
{"title":"Pollution sources and metallic elements mobility recorded by heavy minerals in soils affected by Cu-smelting (Legnica, SW Poland)","authors":"R. Tyszka, A. Pietranik, Beata Marciniak-Maliszewska, Jakub Kierczak","doi":"10.2478/mipo-2024-0001","DOIUrl":"https://doi.org/10.2478/mipo-2024-0001","url":null,"abstract":"\u0000 Heavy mineral particles are widely used in Earth science studies to show sediment provenance and weathering conditions. Such particles are particularly useful in polluted soils surrounding mining and smelting facilities because heavy minerals are common by-products of these activities and may accumulate in the soils. As such, the particles are suitable indicators of metallic element carriers and their stability in the soil environment. In this study, we analyze heavy mineral particles in two soils surrounding the active copper smelter (Legnica, SW, Poland). We show that particles associated with different smelting activities dominate the heavy mineral fraction. We note the general absence of sulfides in the fraction indicating that these minerals might have been entirely dissolved, but timing of this dissolution is uncertain (before or after deposition within soils). Currently, the carriers of potentially toxic elements are mainly secondary Fe oxides. Studies aiming at better estimation of the proportion of metallic elements contained in heavy mineral particles are needed to fully use the potential of these phases in polluted soil studies. We estimate that Pb contained in Pb-rich silicate glass constitutes <0.5% of the total Pb budget and Pb contained in secondary Fe oxides is over 1% of the total budget, but these are minimal estimates.","PeriodicalId":18686,"journal":{"name":"Mineralogia","volume":"26 8","pages":""},"PeriodicalIF":0.0,"publicationDate":"2024-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"140526880","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Karol Faehnrich, Karolina Kośmińska, Jarosław Majka
Abstract Fluid-driven reactions are common in the upper crust, leading to mineral replacement and element redistribution on a kilometer to a micron scale. One common fluid-induced reaction is the chloritization of biotite. Chloritization can lead to the production of multiple phases, such as K-feldspar, titanite, and rutile, depending on local chemistry and fluid composition. Here, we compare different approaches to mass balance calculations using an altered garnet-bearing metapelite collected from Ny Friesland, Svalbard Archipelago, Norway. In the outcrop, amphibolite facies schists are cut by joints that acted as fluid pathways that led to the development of a narrow (~5 cm) alteration zone. Alteration involved the replacement of biotite by chlorite + K-feldspar ± rutile ± titanite. Mass balance calculations based on whole-rock composition and assuming immobile Zr indicate the addition of H 2 O, Si, Ti, Fe, or Mg and the removal of K or Ca. In contrast, mass balance calculated for the pseudomorphic replacement of Bt by Chl + Kfs ± Rt ± Ttn using X-Ray maps for three focused areas indicates the removal of Si or Ti rather than addition. Moles of product phase and elements gained or lost during this reaction varies between individual areas. This variation suggests that fluid heterogeneity and local chemistry governed the progression of the replacement reaction. All the product phases involved in the biotite breakdown are geochronometers and/or geothermometers, providing new opportunities for the petrochronology of fluid-induced reactions.
{"title":"Mass transfer and element redistribution during chloritization of metamorphic biotite in a metapelite: insights from compositional mapping","authors":"Karol Faehnrich, Karolina Kośmińska, Jarosław Majka","doi":"10.2478/mipo-2023-0005","DOIUrl":"https://doi.org/10.2478/mipo-2023-0005","url":null,"abstract":"Abstract Fluid-driven reactions are common in the upper crust, leading to mineral replacement and element redistribution on a kilometer to a micron scale. One common fluid-induced reaction is the chloritization of biotite. Chloritization can lead to the production of multiple phases, such as K-feldspar, titanite, and rutile, depending on local chemistry and fluid composition. Here, we compare different approaches to mass balance calculations using an altered garnet-bearing metapelite collected from Ny Friesland, Svalbard Archipelago, Norway. In the outcrop, amphibolite facies schists are cut by joints that acted as fluid pathways that led to the development of a narrow (~5 cm) alteration zone. Alteration involved the replacement of biotite by chlorite + K-feldspar ± rutile ± titanite. Mass balance calculations based on whole-rock composition and assuming immobile Zr indicate the addition of H 2 O, Si, Ti, Fe, or Mg and the removal of K or Ca. In contrast, mass balance calculated for the pseudomorphic replacement of Bt by Chl + Kfs ± Rt ± Ttn using X-Ray maps for three focused areas indicates the removal of Si or Ti rather than addition. Moles of product phase and elements gained or lost during this reaction varies between individual areas. This variation suggests that fluid heterogeneity and local chemistry governed the progression of the replacement reaction. All the product phases involved in the biotite breakdown are geochronometers and/or geothermometers, providing new opportunities for the petrochronology of fluid-induced reactions.","PeriodicalId":18686,"journal":{"name":"Mineralogia","volume":"222 1","pages":"0"},"PeriodicalIF":0.0,"publicationDate":"2023-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"135502061","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
M. Sachanbiński, Mirosław Kuleba, L. Natkaniec-Nowak
Abstract The authors present the history of chrysoprase discovery and the progress of knowledge about this material over the millennia, based on the extended review of world literature. Tracing the oldest archaeological artifacts from before 9,000 years, the lens of history turns on a stone that has not been properly identified mineralogically for centuries. In the 1830s, chrysoprase was finally included into the chalcedony group and its green color was associated, very correctly, with nickel compounds dispersed in its structure. After all, the most current mineralogy of chrysoprase is presented on the basis of the results of modern analytical studies. These data clearly indicate that chrysoprase is a mixture of several SiO2 polymorphs with varying degrees of structural order (opal, chalcedony, moganite, quartz). This radically changes the previous taxonomy of chrysoprase and its position in current mineralogical and petrographic systematics.
{"title":"Chrysoprase – history and present","authors":"M. Sachanbiński, Mirosław Kuleba, L. Natkaniec-Nowak","doi":"10.2478/mipo-2023-0001","DOIUrl":"https://doi.org/10.2478/mipo-2023-0001","url":null,"abstract":"Abstract The authors present the history of chrysoprase discovery and the progress of knowledge about this material over the millennia, based on the extended review of world literature. Tracing the oldest archaeological artifacts from before 9,000 years, the lens of history turns on a stone that has not been properly identified mineralogically for centuries. In the 1830s, chrysoprase was finally included into the chalcedony group and its green color was associated, very correctly, with nickel compounds dispersed in its structure. After all, the most current mineralogy of chrysoprase is presented on the basis of the results of modern analytical studies. These data clearly indicate that chrysoprase is a mixture of several SiO2 polymorphs with varying degrees of structural order (opal, chalcedony, moganite, quartz). This radically changes the previous taxonomy of chrysoprase and its position in current mineralogical and petrographic systematics.","PeriodicalId":18686,"journal":{"name":"Mineralogia","volume":"1 1","pages":"1 - 10"},"PeriodicalIF":0.0,"publicationDate":"2023-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"88768382","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Eugeniusz Swistun, Maciej Sobczyk, A. S. K. Kumar, W. Tseng, T. Bajda
Abstract Heavy metal toxicity is highly demanding and challenging to clean up the pollutants. To recover the issues mentioned above, we propose a hydrothermal synthesis of zeolite (NaX-UP). Further surface modification by poly-ethylenimine (PEI) could turn to be amine-modified zeolite nanosheets (zeolite NSs) possessed plenty of hydroxyl and amino groups (Al-O, Si-O-Si, Si-OH and NH2) on their surface, decorated with magnetic nanoparticles (Fe3O4 NPs), that are enabled to bridge with inter and intramolecular hydrogen bonding an additionally electrostatic interaction might be a significant role. Further, this can be converted into magnetic bead crosslinking with sodium alginate immersed in an excess calcium chloride solution. The-as formed Fe3O4 NPs decorated amine modified zeolite alginate bead denoted to be (Fe3O4 NPs decorated @PEI-zeolite NSs alginate bead) upholding a significant advantage would aim to clean up the anionic pollutants are [As(V) & V(V)] from an aqueous solution.
{"title":"Synthetic zeolite derived from coal fly ash decorated with magnetic alginate bead: Application to detoxification of arsenic and vanadium","authors":"Eugeniusz Swistun, Maciej Sobczyk, A. S. K. Kumar, W. Tseng, T. Bajda","doi":"10.2478/mipo-2023-0003","DOIUrl":"https://doi.org/10.2478/mipo-2023-0003","url":null,"abstract":"Abstract Heavy metal toxicity is highly demanding and challenging to clean up the pollutants. To recover the issues mentioned above, we propose a hydrothermal synthesis of zeolite (NaX-UP). Further surface modification by poly-ethylenimine (PEI) could turn to be amine-modified zeolite nanosheets (zeolite NSs) possessed plenty of hydroxyl and amino groups (Al-O, Si-O-Si, Si-OH and NH2) on their surface, decorated with magnetic nanoparticles (Fe3O4 NPs), that are enabled to bridge with inter and intramolecular hydrogen bonding an additionally electrostatic interaction might be a significant role. Further, this can be converted into magnetic bead crosslinking with sodium alginate immersed in an excess calcium chloride solution. The-as formed Fe3O4 NPs decorated amine modified zeolite alginate bead denoted to be (Fe3O4 NPs decorated @PEI-zeolite NSs alginate bead) upholding a significant advantage would aim to clean up the anionic pollutants are [As(V) & V(V)] from an aqueous solution.","PeriodicalId":18686,"journal":{"name":"Mineralogia","volume":"64 1","pages":"18 - 29"},"PeriodicalIF":0.0,"publicationDate":"2023-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"77511343","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Abstract Optical microscopy and scanning electron microscopy-energy dispersive X-ray spectroscopy (SEM-EDS) analyses were used to characterize britholite-(Ce) of the metaluminous granite (Proterozoic) intruded into the Nubian Formation in southwestern Egypt and having a relatively high content of radioactive elements (potassium = 4.4 wt%, thorium = 52 ppm, uranium = 10 ppm). The britholite-(Ce) studied here incorporates light rare earth elements (LREE) including lanthanum, cerium, praseodymium, and neodymium as well as thorium. The mineral forms as tabular crystals in a fine-grained quartz-K-feldspar-plagioclase matrix, coexisting with other accessory minerals including biotite, zircon, clinochlore, titanite, and magnetite. Primary britholite-(Ce) usually includes titanite, zircon, and magnetite and is occasionally included in biotite. The inclusion of britholite-(Ce) in biotite suggests that the two minerals crystallized approximately coevally. Petrographical and SEM-EDS data indicate breakdown of the primary magmatic britholite-(Ce) in the samples. This study constitutes the first report for a sole presence of britholite-(Ce) as LREE phase in metaluminous granite samples from Egypt.
{"title":"Britholite-(Ce) from the metaluminous granite of SW Egypt","authors":"K. Hassan","doi":"10.2478/mipo-2023-0002","DOIUrl":"https://doi.org/10.2478/mipo-2023-0002","url":null,"abstract":"Abstract Optical microscopy and scanning electron microscopy-energy dispersive X-ray spectroscopy (SEM-EDS) analyses were used to characterize britholite-(Ce) of the metaluminous granite (Proterozoic) intruded into the Nubian Formation in southwestern Egypt and having a relatively high content of radioactive elements (potassium = 4.4 wt%, thorium = 52 ppm, uranium = 10 ppm). The britholite-(Ce) studied here incorporates light rare earth elements (LREE) including lanthanum, cerium, praseodymium, and neodymium as well as thorium. The mineral forms as tabular crystals in a fine-grained quartz-K-feldspar-plagioclase matrix, coexisting with other accessory minerals including biotite, zircon, clinochlore, titanite, and magnetite. Primary britholite-(Ce) usually includes titanite, zircon, and magnetite and is occasionally included in biotite. The inclusion of britholite-(Ce) in biotite suggests that the two minerals crystallized approximately coevally. Petrographical and SEM-EDS data indicate breakdown of the primary magmatic britholite-(Ce) in the samples. This study constitutes the first report for a sole presence of britholite-(Ce) as LREE phase in metaluminous granite samples from Egypt.","PeriodicalId":18686,"journal":{"name":"Mineralogia","volume":"52 1","pages":"11 - 17"},"PeriodicalIF":0.0,"publicationDate":"2023-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"86701178","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Abstract Talc is crystallized in the metamorphic dolomitic rocks of the southwest Pamir mountains in the Mulvoj area, Tajikistan. Field studies show that talc is restricted to metamorphic dolomitic marble layers in the garnet-mica schist and gneiss. The layers are parallel to the original sedimentary bedding and schistosity of the metamorphic rocks. Petrography and whole rock geochemistry reveal calcite, tremolite, quartz and dolomite as the main mineral phases in the talc-bearing metamorphosed dolomitic rocks, while calcite is absent in the samples without talc. XRD studies show that talc samples are almost pure, and geochemistry indicates very low Fe and Cr and very high Mg contents. Geochemical features along with field observations clearly shows that Mulvoj talc is not originated from peridotite. Based on phase relations studies in the CaO-MgO-SiO2-H2O-CO2 system, the reaction between dolomite, quartz, and water at pressure greater than 2 kbar and temperature up to ~460°C and XCO2 up to 0.6 was the main talc forming reaction. Talc and calcite consuming reaction produced tremolite, dolomite and binary (CO2-H2O) fluid.
{"title":"Metamorphic dolomitic marble-hosted talc from the Mulvoj area in the Western Pamir Mountains, Tajikistan","authors":"M. Moazzen, Intizor Silmonov, S. Elnazarov","doi":"10.2478/mipo-2023-0004","DOIUrl":"https://doi.org/10.2478/mipo-2023-0004","url":null,"abstract":"Abstract Talc is crystallized in the metamorphic dolomitic rocks of the southwest Pamir mountains in the Mulvoj area, Tajikistan. Field studies show that talc is restricted to metamorphic dolomitic marble layers in the garnet-mica schist and gneiss. The layers are parallel to the original sedimentary bedding and schistosity of the metamorphic rocks. Petrography and whole rock geochemistry reveal calcite, tremolite, quartz and dolomite as the main mineral phases in the talc-bearing metamorphosed dolomitic rocks, while calcite is absent in the samples without talc. XRD studies show that talc samples are almost pure, and geochemistry indicates very low Fe and Cr and very high Mg contents. Geochemical features along with field observations clearly shows that Mulvoj talc is not originated from peridotite. Based on phase relations studies in the CaO-MgO-SiO2-H2O-CO2 system, the reaction between dolomite, quartz, and water at pressure greater than 2 kbar and temperature up to ~460°C and XCO2 up to 0.6 was the main talc forming reaction. Talc and calcite consuming reaction produced tremolite, dolomite and binary (CO2-H2O) fluid.","PeriodicalId":18686,"journal":{"name":"Mineralogia","volume":"45 1","pages":"30 - 41"},"PeriodicalIF":0.0,"publicationDate":"2023-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"86674793","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Abstract The lime plasters of the excavated monument of Salvankuppam, previously submerged and exposed by the Tsunami occurred in the Indian Ocean on 26th December 2004 was studied with different analytical techniques. The temple is dated 4-5th century CE. The XRF, XRD, FTIR, NMR, SEM-EDX analysis of the lime plasters evidenced particular occurrence of phosphatised bacterial remains in saline conditions. The formation of amorphous Ca-phosphate by bio mineralization was identified in the plasters by the analyses. The plasters are made of air-lime with coarse aggregates and seashells inclusion as confirmed by the thermal and chemical analysis. The microstructure and morphological investigations of mineralized microbial structures by SEM-EDX indicated the formation of amorphous Ca-phosphate. The unordered and fibrous spherulites have hardened and reduced porosity of the plaster by bio mineralization as observed through MIP analysis. The 16S rRNA sequencing has identified the Pseudomonas strains mainly responsible for the clustering of amorphous Ca-phosphate particles around the bacterial colony.
{"title":"Evidence of amorphous Ca-phosphate precipitate caused by bio mineralisation in 4-5th CE lime plasters of the previously submerged east coastal monument of Salvankuppam","authors":"M. Singh, S. V. Kumar, K. Ganaraj","doi":"10.2478/mipo-2021-0003","DOIUrl":"https://doi.org/10.2478/mipo-2021-0003","url":null,"abstract":"Abstract The lime plasters of the excavated monument of Salvankuppam, previously submerged and exposed by the Tsunami occurred in the Indian Ocean on 26th December 2004 was studied with different analytical techniques. The temple is dated 4-5th century CE. The XRF, XRD, FTIR, NMR, SEM-EDX analysis of the lime plasters evidenced particular occurrence of phosphatised bacterial remains in saline conditions. The formation of amorphous Ca-phosphate by bio mineralization was identified in the plasters by the analyses. The plasters are made of air-lime with coarse aggregates and seashells inclusion as confirmed by the thermal and chemical analysis. The microstructure and morphological investigations of mineralized microbial structures by SEM-EDX indicated the formation of amorphous Ca-phosphate. The unordered and fibrous spherulites have hardened and reduced porosity of the plaster by bio mineralization as observed through MIP analysis. The 16S rRNA sequencing has identified the Pseudomonas strains mainly responsible for the clustering of amorphous Ca-phosphate particles around the bacterial colony.","PeriodicalId":18686,"journal":{"name":"Mineralogia","volume":"11 1","pages":"19 - 30"},"PeriodicalIF":0.0,"publicationDate":"2022-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"81899602","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Abstract We used spider webs as a particulate matter (PM) sampler to assess the possible health risk to the inhabitants of Legnica city (Poland). We aimed to find out if it is a useful material and could provide reliable information. We selected two spider families (Agelenidae and Linyphiidae) whose webs structure enhances the PM accumulation. The collected particles were analysed using a Scanning Electron Microscope equipped with Energy Dispersive X-Ray (SEM-EDX) and Inductively Coupled Plasma Mass Spectrometry (ICP-MS) which provided morphological and chemical information and allowed to indicate possible sources of pollution. The results showed that PM10, the fraction of particles smaller than 10 µm, was dominated by the particles of natural origin, while fine fractions were composed of diverse anthropogenic particles, whose origin can be connected with the activity of the copper smelter and in smaller quantity with the road traffic. The carcinogenic and non-carcinogenic health risk was assessed for these pathways: inhalation, ingestion, and dermal, for children and adults. The non-carcinogenic risk was very high (Hazard Index: HI > 1) both for children (Cu, Ni, Pb, Cd) and adults (Cu, As, Pb, Cd). Moreover, high carcinogenic risk (>10-4) was found in most of the sampling points. The study shows that spider webs are useful in biomonitoring of PM and can also be used for health risk assessment. In the studied region, it was found that the possible negative impact of air pollution on human health exists.
{"title":"Health risk assessment in the vicinity of a copper smelter: particulate matter collected on a spider web","authors":"Agnieszka Trzyna, J. Rybak, W. Bartz, M. Górka","doi":"10.2478/mipo-2022-0004","DOIUrl":"https://doi.org/10.2478/mipo-2022-0004","url":null,"abstract":"Abstract We used spider webs as a particulate matter (PM) sampler to assess the possible health risk to the inhabitants of Legnica city (Poland). We aimed to find out if it is a useful material and could provide reliable information. We selected two spider families (Agelenidae and Linyphiidae) whose webs structure enhances the PM accumulation. The collected particles were analysed using a Scanning Electron Microscope equipped with Energy Dispersive X-Ray (SEM-EDX) and Inductively Coupled Plasma Mass Spectrometry (ICP-MS) which provided morphological and chemical information and allowed to indicate possible sources of pollution. The results showed that PM10, the fraction of particles smaller than 10 µm, was dominated by the particles of natural origin, while fine fractions were composed of diverse anthropogenic particles, whose origin can be connected with the activity of the copper smelter and in smaller quantity with the road traffic. The carcinogenic and non-carcinogenic health risk was assessed for these pathways: inhalation, ingestion, and dermal, for children and adults. The non-carcinogenic risk was very high (Hazard Index: HI > 1) both for children (Cu, Ni, Pb, Cd) and adults (Cu, As, Pb, Cd). Moreover, high carcinogenic risk (>10-4) was found in most of the sampling points. The study shows that spider webs are useful in biomonitoring of PM and can also be used for health risk assessment. In the studied region, it was found that the possible negative impact of air pollution on human health exists.","PeriodicalId":18686,"journal":{"name":"Mineralogia","volume":"37 1","pages":"36 - 50"},"PeriodicalIF":0.0,"publicationDate":"2022-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"86354526","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Abstract The present work reports the first anatectic melt inclusions found so far in the Mesoarchean basement in East Greenland. Using optical microscope observations and MicroRaman spectroscopy, we show that garnets in metasedimentary migmatite contain primary polycrystalline aggregates which can be confidently interpreted as former droplets of anatectic melt, i.e. nanogranitoids. In some cases, they coexist with coeval fluid inclusions under conditions of primary fluid-melt immiscibility. The re-evaluation of the metamorphic pressure and temperature conditions with up-to-date phase equilibria modelling, combined with the identification of nanogranitoids and fluid inclusions, suggests metamorphic peak equilibration and partial melting in presence of a COH-fluid at T ~1000°C and P > 7 kbar. To date, this is the oldest verified occurrence of nanogranitoids and fluid-melt immiscibility during garnet growth in a partially molten environment.
{"title":"Mesoarchean melt and fluid inclusions in garnet from the Kangerlussuaq basement, Southeast Greenland","authors":"G. Nicoli, Kerstin Gresky, S. Ferrero","doi":"10.2478/mipo-2022-0001","DOIUrl":"https://doi.org/10.2478/mipo-2022-0001","url":null,"abstract":"Abstract The present work reports the first anatectic melt inclusions found so far in the Mesoarchean basement in East Greenland. Using optical microscope observations and MicroRaman spectroscopy, we show that garnets in metasedimentary migmatite contain primary polycrystalline aggregates which can be confidently interpreted as former droplets of anatectic melt, i.e. nanogranitoids. In some cases, they coexist with coeval fluid inclusions under conditions of primary fluid-melt immiscibility. The re-evaluation of the metamorphic pressure and temperature conditions with up-to-date phase equilibria modelling, combined with the identification of nanogranitoids and fluid inclusions, suggests metamorphic peak equilibration and partial melting in presence of a COH-fluid at T ~1000°C and P > 7 kbar. To date, this is the oldest verified occurrence of nanogranitoids and fluid-melt immiscibility during garnet growth in a partially molten environment.","PeriodicalId":18686,"journal":{"name":"Mineralogia","volume":"28 1","pages":"1 - 9"},"PeriodicalIF":0.0,"publicationDate":"2022-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"78468935","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Abstract The high temperature decomposition of basalt from Lower Silesia (Poland) was followed by Mössbauer spectroscopy investigation. The Fe content of the sample was ~9.0 at.%. The X-ray diffraction analysis shows that augite (37%) and olivine (12%) are major Fe-bearing mineral components. The sample also contains significant amount of anorthite (22%) and nepheline (17%). The sample was heated at various temperatures between 200°C and 1100°C for three hours. Up to a temperature of 500°C changes in contribution of Fe-bearing minerals are insignificant. Heating in the temperature range from 500°C to 1100°C leads to a systematic increase in contribution of iron oxides at the cost of contribution of silicate minerals, like augite and olivine. Mössbauer spectrum obtained after heating at 1100°C showed hematite as the main iron oxide phase. The ratio of Fe3+/Fetot in the non-heated sample was equal to 0.51 and after heating at 1100°C this ratio amounted to 0.89.
{"title":"High temperature transformation of iron-bearing minerals in basalt: Mössbauer spectroscopy studies","authors":"M. Kądziołka-Gaweł, M. Wojtyniak, J. Klimontko","doi":"10.2478/mipo-2022-0002","DOIUrl":"https://doi.org/10.2478/mipo-2022-0002","url":null,"abstract":"Abstract The high temperature decomposition of basalt from Lower Silesia (Poland) was followed by Mössbauer spectroscopy investigation. The Fe content of the sample was ~9.0 at.%. The X-ray diffraction analysis shows that augite (37%) and olivine (12%) are major Fe-bearing mineral components. The sample also contains significant amount of anorthite (22%) and nepheline (17%). The sample was heated at various temperatures between 200°C and 1100°C for three hours. Up to a temperature of 500°C changes in contribution of Fe-bearing minerals are insignificant. Heating in the temperature range from 500°C to 1100°C leads to a systematic increase in contribution of iron oxides at the cost of contribution of silicate minerals, like augite and olivine. Mössbauer spectrum obtained after heating at 1100°C showed hematite as the main iron oxide phase. The ratio of Fe3+/Fetot in the non-heated sample was equal to 0.51 and after heating at 1100°C this ratio amounted to 0.89.","PeriodicalId":18686,"journal":{"name":"Mineralogia","volume":"73 1","pages":"10 - 19"},"PeriodicalIF":0.0,"publicationDate":"2022-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"80039601","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
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