carbonate material
Recently Published Documents


TOTAL DOCUMENTS

48
(FIVE YEARS 22)

H-INDEX

6
(FIVE YEARS 1)

2022 ◽  
Author(s):  
Katarzyna Stanienda-Pilecki

Abstract The results of researches of the stable isotopes, carbon 13C and oxygen 18O, measured in Triassic limestones of Opole Silesia in Poland were presented in this article. The study was carried out to obtain data for interpretation of the environment of these rocks formation. Moreover, it was possible to form the theory about diagenetic processes which influenced on the mineral composition of limestone and some of their carbonte phases. The results of study show a general differentiation of δ13C and δ18O contents in carbonate minerals. All δ18O values are less than 0 ‰. It indicates that the origin oxygen isotope composition could be probably reset by diagenesis. The crystallization temperatures of low-Mg calcite and high-Mg, calculated on the basis of δ18O values are greater than 25 oC. They are higher than typical for sea basin and are also not be related to the presence of hydrothermal solutions. The increased temperatures of calcites crystallization are related to diagenetic processes that took place after the deposition and burial of carbonate material. The preservation of high-Mg calcite, an ustable carbonate phase, which is usually trasformed into low-Mg calcite during diagenesis, is probably connected with the increased salinity of the sea basin in which studied limestones were formed.


10.5219/1591 ◽  
2021 ◽  
Vol 15 ◽  
pp. 877-890
Author(s):  
Tatiana Kos ◽  
Inha Kuznietsova ◽  
Tamila Sheiko ◽  
Liubomyr Khomichak ◽  
Yuliia Kambulova ◽  
...  

In the article it is offered to enter in the technological audit of the lime department of sugar factory the adjusted technique of the definition of the maintenance of calcium carbonate in carbonate breed. For this purpose, a complete chemical analysis of limestone was performed, which includes determination of moisture content, impurities insoluble in hydrochloric acid, the amount of one and a half oxides of aluminum and iron, calcium carbonate (advanced method), and magnesium carbonate, calcium sulfate, alkali metal oxides, potassium, and sodium. The obtained experimental data are summarized in one table and the material balance of all components of carbonate bedrock is summarized. The proposed method made it possible to obtain objective data on the component composition of the carbonate material. This, in turn, avoids many technological problems, namely to reduce the formation of melts in the lime kiln, improve the filtration of juices, increase the ability of lime to chemically interact with water, reduce the volume of water on the juicer etc. Thus, the use of the recommended method for determining calcium carbonate (CaCO3), as part of the technological audit, will allow early adjustment of the process, which will give maximum energy and resource savings, as well as increase the level of environmental friendliness of the enterprise.


Geosciences ◽  
2021 ◽  
Vol 11 (9) ◽  
pp. 360
Author(s):  
Cannata Chiara Benedetta ◽  
De Rosa Rosanna ◽  
Donato Paola ◽  
Morrone Consuele ◽  
Muto Francesco

Evidence of volcaniclastic sedimentation occurs in the first depositional sequence of the sedimentary succession of the Amantea Basin. Volcaniclastic deposits are intercalated in the upper part of a sandstone formation and these show a maximum thickness of about 8 m. The Amantea Basin is a Neogene depozone located along the Tyrrhenian margin of Calabria whose onset started during the Upper Serravallian. The source volcano to these materials had to have been located within or near to the marine basin in order to supply it with significant amounts of pyroclastic fragments emplaced by either pyroclastic fall/or flows during one or more explosive eruptions. The marine environment of volcaniclastic flows made up of pyroclastic fragments mixed with minor siliciclastic and carbonate material. The textural and structural features of the deposits and the composition of the volcanic glass fragments indicate an origin from a sub-aerial coeval explosive eruption, with initial sedimentation in a shallow marine environment, mixing with non-volcanic materials, reworking and final re-sedimentation into the basin. The age of the volcaniclastic/sedimentary sequence makes these deposits a marker for the geodynamic evolution of the area, and the lack of such horizons in the other coeval peri-Tyrrhenian basins allows us to consider the Amantea Basin as a confined elongated coastal basin area, whose tectonostratigraphic architecture denotes a structural partitioning of the eastern nascent Tyrrhenian Basin.


2021 ◽  
Vol 18 (16) ◽  
pp. 4733-4753
Author(s):  
Nicolai Schleinkofer ◽  
David Evans ◽  
Max Wisshak ◽  
Janina Vanessa Büscher ◽  
Jens Fiebig ◽  
...  

Abstract. Hyrrokkin sarcophaga is a parasitic foraminifera that is commonly found in cold-water coral reefs where it infests the file clam Acesta excavata and the scleractinian coral Desmophyllum pertusum (formerly known as Lophelia pertusa). Here, we present measurements of the trace element and isotopic composition of these parasitic foraminifera, analyzed by inductively coupled optical emission spectrometry (ICP-OES), electron probe microanalysis (EPMA) and mass spectrometry (gas-source MS and inductively-coupled-plasma MS). Our results reveal that the geochemical signature of H. sarcophaga depends on the host organism it infests. Sr / Ca ratios are 1.1 mmol mol−1 higher in H. sarcophaga that infest D. pertusum, which could be an indication that dissolved host carbonate material is utilized in shell calcification, given that the aragonite of D. pertusum has a naturally higher Sr concentration compared to the calcite of A. excavata. Similarly, we measure 3.1 ‰ lower δ13C and 0.25 ‰ lower δ18O values in H. sarcophaga that lived on D. pertusum, which might be caused by the direct uptake of the host's carbonate material with a more negative isotopic composition or different pH regimes in these foraminifera (pH can exert a control on the extent of CO2 hydration/hydroxylation) due to the uptake of body fluids of the host. We also observe higher Mn / Ca ratios in foraminifera that lived on A. excavata but did not penetrate the host shell compared to specimen that penetrated the shell, which could be interpreted as a change in food source, changes in the calcification rate, Rayleigh fractionation or changing oxygen conditions. While our measurements provide an interesting insight into the calcification process of this unusual foraminifera, these data also indicate that the geochemistry of this parasitic foraminifera is unlikely to be a reliable indicator of paleoenvironmental conditions using Sr / Ca, Mn / Ca, δ18O or δ13C unless the host organism is known and its geochemical composition can be accounted for.


2021 ◽  
Vol 17 (4) ◽  
pp. 1607-1625
Author(s):  
Dustin T. Harper ◽  
Marina B. Suarez ◽  
Jessica Uglesich ◽  
Hailu You ◽  
Daqing Li ◽  
...  

Abstract. The Early Cretaceous is characterized by warm background temperatures (i.e., greenhouse climate) and carbon cycle perturbations that are often marked by ocean anoxic events (OAEs) and associated shifts in the hydrologic cycle. Higher-resolution records of terrestrial and marine δ13C and δ18O (both carbonates and organics) suggest climate shifts during the Aptian–Albian, including a warm period associated with OAE 1a in the early Aptian and a subsequent “cold snap” near the Aptian–Albian boundary prior to the Kilian and OAE 1b. Understanding the continental system is an important factor in determining the triggers and feedbacks to these events. Here, we present new paleosol carbonate stable isotopic (δ13C, δ18O and Δ47) and CALMAG weathering parameter results from the Xiagou and Zhonggou formations (part of the Xinminpu Group in the Yujingzi Basin of NW China) spanning the Aptian–Albian. Published mean annual air temperature (MAAT) records of the Barremian–Albian from Asia are relatively cool with respect to the Early Cretaceous. However, these records are largely based on coupled δ18O measurements of dinosaur apatite phosphate (δ18Op) and carbonate (δ18Ocarb) and therefore rely on estimates of meteoric water δ18O (δ18Omw) from δ18Op. Significant shifts in the hydrologic cycle likely influenced δ18Omw in the region, complicating these MAAT estimates. Thus, temperature records independent of δ18Omw (e.g., clumped isotopes or Δ47) are desirable and required to confirm temperatures estimated with δ18Op and δ18Oc and to reliably determine regional shifts in δ18Omw. Primary carbonate material was identified using traditional petrography, cathodoluminescence inspection, and δ13C and δ18O subsampling. Our preliminary Δ47-based temperature reconstructions (record mean of 14.9 ∘C), which we interpret as likely being representative of MAAT, match prior estimates from similar paleolatitudes of Asian MAAT (average ∼ 15 ∘C) across the Aptian–Albian. This, supported by our estimated mean atmospheric paleo-pCO2 concentration of 396 ppmv, indicates relatively cooler midlatitude terrestrial climate. Additionally, our coupled δ18O and Δ47 records suggest shifts in the regional hydrologic cycle (i.e., ΔMAP, mean annual precipitation, and Δδ18Omw) that may track Aptian–Albian climate perturbations (i.e., a drying of Asian continental climate associated with the cool interval).


Minerals ◽  
2021 ◽  
Vol 11 (7) ◽  
pp. 666
Author(s):  
Anatoly V. Nikiforov ◽  
Elena O. Dubinina ◽  
Nikolay A. Polyakov ◽  
Amina M. Sugorakova ◽  
Aylan K. Khertek

The study of the O and C isotope composition of calcite from nepheline syenites, ijolites and carbonatites of the Chik intrusion and the intrusions of the Erzin–Tarbagatay group of Sangilen (Eastern Siberia, Russia) showed derivation from alkaline melts enriched with a carbonate component from the host marbleized sedimentary rocks. The calculations showed that about 40% of the initial mass of carbonates involved in the interaction with silicate melts have remained after decarbonation. During the assimilation of the carbonate, an oxygen isotope exchange took place between the residual carbonate material and the silicate phase. Crystallization products of such hybrid magmas are carbonatite veins, calcite-rich nepheline rocks and their pegmatites with a calcite core.


Minerals ◽  
2021 ◽  
Vol 11 (6) ◽  
pp. 654
Author(s):  
Eugene V. Sklyarov ◽  
Andrey V. Lavrenchuk ◽  
Anna G. Doroshkevich ◽  
Anastasia E. Starikova ◽  
Sergei V. Kanakin

Pyroxenite and nepheline-pyroxene rocks coexist with dolomite-bearing calcite marbles in Tazheran Massif in the area of Lake Baikal, Siberia, Russia. Pyroxenites occur in a continuous elongate zone between marbles and beerbachites (metamorphosed gabbro dolerites) and in 5 cm to 20 m fragments among the marbles. Pyroxene in pyroxenite is rich in calcium and alumina (5–12 wt% Al2O3) and has a fassaite composition. The Tazheran pyroxenite may originate from a mafic subvolcanic source indicated by the presence of remnant dolerite found in one pyroxenite body. This origin can be explained in terms of interaction between mafic and crust-derived carbonatitic melts, judging by the mineralogy of pyroxenite bodies and their geological relations with marbles. According to this model, the intrusion of mantle mafic melts into thick lower crust saturated with fluids caused partial melting of silicate-carbonate material and produced carbonate and carbonate-silicate melts. The fassaite-bearing pyroxenite crystallized from a silicate-carbonate melt mixture which was produced by roughly synchronous injections of mafic, pyroxenitic, and carbonate melt batches. The ascending hydrous carbonate melts entrained fragments of pyroxenite that crystallized previously at a temperature exceeding the crystallization point of carbonates. Subsequently, while the whole magmatic system was cooling down, pyroxenite became metasomatized by circulating fluids, which led to the formation of assemblages with garnet, melilite, and scapolite.


2021 ◽  
Author(s):  
Katarzyna Jadwiga Stanienda-Pilecki

Abstract The results of researches of the selected trace elements: Ti, Sr, Ba, Zn, and also Cr, Ni, Cu, Zr, Mo, Pb, Rb, Mn, Na, K, P, Y and REE (REY) content were presented in this article. The elements were measured in the carbonate minerals of Muschelkalk (Middle Triassic) limestones of the Opole Silesia in Poland, using two methods: ICP MS spectrometry and X-ray fluorescence. These methods are characterized by very high precision and sensitivity of measurements. The results of researches show that the content of analyzed trace elements varies in from value below 1 ppm up to some hundreds ppm. However, the highest contents were measured for strontium and barium, elements characteristic for aragonite carbonate phase which is transformed such as high-Mg calcite into low magnesium calcite during diagenesis. So as Sr and Ba indicate the presence of aragonite in the primary carbonate material. The other trace elements probably form substitutions in clay or carbonate minerals. Some of trace elements such as Zn, Pb, Cu, Mo, Ni may also be associated with sulfide minerals and Ti, Cr, Mn, with oxides. Some measured REY elements- Ce, Nd, Sm, Gd, Dy, Er and Y are found in the rocks in very small quantities. So their content is really very low. It varies in from value below 1 ppm up to 6 ppm. REY usually substitute Ca ions in calcite.


MRS Advances ◽  
2021 ◽  
Author(s):  
Jonathan B. Junio ◽  
Prae Chirawatkul ◽  
Marlon T. Conato ◽  
Candy C. Mercado

AbstractTin (Sn2+) and strontium (Sr2+), two potential alternatives to lead (Pb2+) in perovskite formation, were explored in transforming calcium carbonate (CaCO3) into a leaving group in a cation exchange reaction. This is the first part of a sequential ion exchange process in transforming calcite into a Pb-free perovskite material for perovskite solar cell applications. Calcite, a polymorph of CaCO3, was successfully transformed into strontianite (SrCO3) through a cation exchange reaction. In the Sn substitution reaction on the other hand, no SnCO3 formation was noted. Instead, oxides of Sn were formed. The wider spaces in between Ca2+ cations in (100) orientation account for the higher atomic Sn2+ and Sr2+ concentrations as compared to (001) orientation, where the cation movement is restricted. X-ray absorption and photoelectron spectroscopies were used to investigate the ion-exchange transformation of calcite towards the formation of an intermediate carbonate material. Graphic abstract


2021 ◽  
Author(s):  
Nicolai Schleinkofer ◽  
David Evans ◽  
Max Wisshak ◽  
Janina Vanessa Büscher ◽  
Jens Fiebig ◽  
...  

Abstract. Hyrrokkin sarcophaga is a parasitic foraminifer that is commonly found in cold-water coral reefs where it infests the file clam Acesta excavata and the scleractinian coral Lophelia pertusa. Here, we present measurements of the elemental and isotopic composition of this parasitic foraminifer for the first time, analyzed by inductively coupled optical emission spectrometry (ICP-OES), electron probe micro analysis (EPMA) and mass spectrometry (MS).Our results reveal that the geochemical signature of H. sarcophaga depends on the host organism it infests. Sr/Ca ratios are 1.1 mmol mol−1 higher in H. sarcophaga that infest L. pertusa, which could be an indication that dissolved host carbonate material is utilised in shell calcification, given that the aragonite of L. pertusa has a naturally higher Sr concentration compared to the calcite of A. excavata. Similarly, we measure 3.1 ‰ lower δ13C and 0.25 ‰ lower δ18O values in H. sarcophaga that lived on L. pertusa, which might be caused by the direct uptake of the host's carbonate material with a more negative isotopic composition or different pH regimes in these foraminifera (pH can exert a control on the extent of CO2 hydration/hydroxylation) due to the uptake of body fluids of the host. We also observe higher Mn/Ca ratios in foraminifers that lived on A. excavata but did not penetrate the host shell compared to specimen that penetrated the shell, which could be interpreted as a change in food source, changes in the calcification rate, Rayleigh fractionation or changing oxygen conditions.While our measurements provide an interesting insight into the calcification process of this unusual foraminifer, these data also indicate that the geochemistry of this parasitic foraminifer is unlikely to be a reliable indicator of paleoenvironmental conditions using Sr/Ca, Mn/Ca, δ18O or δ13C unless the host organism is known and its geochemical composition can be accounted for.


Sign in / Sign up

Export Citation Format

Share Document