Geochemistry International最新文献

{"title":"Humification of the Organic Matter in the Surface Bottom Sediments of the East Siberian Sea","authors":"A. A. Mariash,&nbsp;K. I. Aksentov,&nbsp;M. V. Ivanov","doi":"10.1134/S0016702924601864","DOIUrl":"10.1134/S0016702924601864","url":null,"abstract":"<p>New data on the content of humic substances (HS) in the East Siberian Sea are presented. The results of the studies showed that the degree of humification of organic matter (OM) in the studied samples of the upper layer of bottom sediments of the sea varies from 21 to 9% and averages 15%, which is typical of the low-productivity Arctic seas. It was found that the average HS values (for the considered profiles) were 0.16 and 0.20%, which is typical of oxidized marine sediments. The concentration of organic carbon (C_org) varied from 0.34 to 1.89% depending on the granulometric type of sediment. It is shown that the total C_org consists of 10–40% HS, and the HS themselves consist of 12–30% humic acids (HA) and 70–88% fulvic acids (FA), which indicates the early humification of sediments. НAs were determined only in the sediments of the coastal part of the sea. FAs were determined in all studied bottom sediments.</p>","PeriodicalId":12781,"journal":{"name":"Geochemistry International","volume":"63 4","pages":"321 - 331"},"PeriodicalIF":0.7,"publicationDate":"2025-05-23","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"144117600","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"地球科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}

{"title":"A New Reaction Controlling the Composition of Oils: Hydrogenation of Aromatic Hydrocarbons","authors":"M. B. Smirnov,&nbsp;N. A. Vanyukova","doi":"10.1134/S0016702924601268","DOIUrl":"10.1134/S0016702924601268","url":null,"abstract":"<p>Analysis of the composition of <i>n</i>-alkyl-substituted monocyclic compounds (<i>n</i>-alkylcyclohexanes, <i>n</i>-alkylcyclopentanes, and <i>n</i>-alkylbenzenes) of Tatarstan oils made it possible to prove that the composition of the oils was controlled by still another reaction, whose evidence has never before been identified in rocks: the hydrogenation reaction of aromatic hydrocarbons. It has been directly proven that <i>n</i>-alkylcyclohexanes of the oils were partially formed from <i>n</i>-alkylbenzenes of these oils. Therewith catalysts for the hydrogenation of aromatic hydrocarbons known in organic chemistry either are not present in any noticeable quantities in oils (as are platinum-group metals in the Earth’s crust) or are inactive in natural environments, and hence, it is not possible to indicate any natural catalyst for this reaction. Thus, the discovery of this reaction demonstrates the incompleteness of our understanding of the catalysts involved in the formation of the composition of oils. Literature data indicate that Tatarstan is not the only region in whose oils this reaction occurs. It is demonstrated that the oils should have occurred during their hydrogenation under conditions radically different from those that occurred during the formation of their main components (acid catalysts occurring during the first stage and absent during the second one). It follows that the hydrogenation reaction of aromatic hydrocarbons in Tatarstan oils operated during the later stages of their evolution, when the main composition of the oils had already been formed. It seems to be reasonable to assume that hydrogenation took place after the migration of oil from the source rock, i.e., this reaction operated either during oil migration routes or in the reservoir.</p>","PeriodicalId":12781,"journal":{"name":"Geochemistry International","volume":"63 4","pages":"332 - 340"},"PeriodicalIF":0.7,"publicationDate":"2025-05-23","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"144117601","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"地球科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}

{"title":"Distribution of Hydrocarbon Biomarkers with Depth in Marine Sediments in the Area of the Linear Depression of the West Kara Stage","authors":"V. S. Sevastyanov,&nbsp;V. S. Fedulov,&nbsp;V. Yu. Fedulova,&nbsp;R. H. Dzhenloda,&nbsp;N. V. Dushenko,&nbsp;S. A. Voropaev","doi":"10.1134/S0016702924601050","DOIUrl":"10.1134/S0016702924601050","url":null,"abstract":"<p>Studies of molecular and hydrocarbon composition of marine sediments provide important information on sedimentary organic matter (OM). In this work, the distribution of hydrocarbons and molecular markers with depth in the sedimentary cover of the linear depression of the West Kara stage was studied. To do this, two sediment cores were sampled during 89^th cruise of the R/V Akademik Mstislav Keldysh at site 7444 and at background site 7441. The distribution of n-alkanes was measured by GC-MS analysis, and the distribution patterns of the biomarker indices of sedimentary OM in the marine sediments with depth were determined. It was shown that higher terrestrial vegetation was the dominant source to the sedimentary OM of marine sediments at sites 7444 and 7441. The OM is of low maturity, as follows from its Ts/(Ts + Tm) ratio. According to the values of H31-S/H31-(S + R) and NAR indices, a small constant inflow of oil hydrocarbons occurs in the study area, and a much lower inflow takes place at background site 7441. The distribution of the CPI25–33, TAR, and NAR suggest that hydrocarbons of anthropogenic origin occur in the near-surface layers of 0–15 cm sediment at background site 7441.</p>","PeriodicalId":12781,"journal":{"name":"Geochemistry International","volume":"63 4","pages":"307 - 320"},"PeriodicalIF":0.7,"publicationDate":"2025-05-23","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"144117737","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"地球科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}

{"title":"Elemental Composition and Sources of Urban Dust of a Large Industrial City (Krasnoyarsk, Russia)","authors":"A. I. Ivaneev,&nbsp;A. S. Brzhezinskiy,&nbsp;V. K. Karandashev,&nbsp;M. S. Ermolin,&nbsp;P. S. Fedotov","doi":"10.1134/S0016702924601566","DOIUrl":"10.1134/S0016702924601566","url":null,"abstract":"<p>This paper reports the first comprehensive study of urban dust from Krasnoyarsk. The elemental composition of the dust was determined, and several natural and anthropogenic sources of its formation were distinguished. Dust samples (<i>n</i> = 68) were collected in different functional regions of the city. The contents of 70 elements were measured in the dust samples. The (CaO + Na₂O)–Al₂O₃–K₂O and (CaO + Na₂O + K₂O)–Al₂O₃–(Fe₂O₃ + MgO) diagrams showed that the mineral component of most of the Krasnoyarsk dust samples is dominated by plagioclases. The calculation of enrichment factors and geoaccumulation indices showed that the Krasnoyarsk dust is enriched by Co, Sn, Ni, Pb, Mo, Cu, As, Zn, Cd, W, Ag, and Sb. The characteristics of trace element accumulation depending on sampling locality were evaluated. Antimony is accumulated mainly in samples from major highways of Krasnoyarsk, whereas elevated As, Cu, W, and Zn contents were usually found in samples collected in industrial zones of the city. Using principal component analysis and the Pearson correlation matrix, six groups of elements were distinguished in the dust samples, and their natural and anthropogenic sources were determined: Al, Ti, Cr, Fe, and Ni were supplied by soil and rock weathering; Fe, Co, Ni, Cu, and As, emissions from metallurgical plants and coal-burning thermal power plants; W, Bi, Zn, and Mo, heavy metallurgical and mechanical engineering industries; Cu, Cd, Sn, and Pb, emissions of motor and rail transport, as well as wear of metal parts and structures; Sn and Sb, wear of brake pads and tires and industrial emissions; and Hg, soil and rock weathering.</p>","PeriodicalId":12781,"journal":{"name":"Geochemistry International","volume":"63 4","pages":"341 - 360"},"PeriodicalIF":0.7,"publicationDate":"2025-05-23","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"144117623","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"地球科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}

{"title":"Physico-Chemical Mechanisms of Formation of Concentrically Banded Agates in Basalts: Hypotheses and Experiments","authors":"V. A. Alekseyev,&nbsp;D. V. Korost,&nbsp;N. V. Stepanov,&nbsp;A. V. Mokhov,&nbsp;I. N. Gromyak","doi":"10.1134/S0016702924601165","DOIUrl":"10.1134/S0016702924601165","url":null,"abstract":"<p>Based on literature data, the main properties of agates and the conditions of their formation are summarized, and a critical analysis of the hypotheses of agate formation is performed. The hypothesis of layerwise precipitation and crystallization of silica extracted from the host rock (in particular, basalt) turned out to be the most adequate. However, difficulties remained in explaining the SiO₂ movement from the host basalt to the agate cavities, the causes of SiO₂ precipitation, the role of phase transformations, and the mechanism of banding formation. To clarify these questions, experiments were performed on the dissolution of basalt samples in water for 4 months at 300°C. The formation of silica was noticeable only in experiments where the basalt sample was half-submerged in water. In particular, amorphous silica (opal-A) was precipitated in the pores and on the sample surface above the water level, which formed agate-like layered textures and was replaced in places by chalcedony. The experimental results are explained within the framework of the distillation hypothesis, which may be suitable for the formation of agates. The hypothesis combines the possibilities of SiO₂ transfer in low-concentration regions and its precipitation in high-concentration regions, and also explains the agate banding by fluctuations in supply and consumption of dissolved silica in precipitation and phase transformation reactions.</p>","PeriodicalId":12781,"journal":{"name":"Geochemistry International","volume":"63 3","pages":"259 - 273"},"PeriodicalIF":0.7,"publicationDate":"2025-04-14","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143826597","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"地球科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}

{"title":"Reconstructed Characteristics of the Initial Melt of the Kaalamo Multiphase Clinopyroxenite–Gabbronorite–Diorite Intrusion, Northern Ladoga Area, Southern Karelia","authors":"R. L. Anisimov,&nbsp;Sh. K. Baltybaev,&nbsp;A. A. Ariskin,&nbsp;M. E. Petrakova,&nbsp;E. S. Bogomolov","doi":"10.1134/S0016702924601554","DOIUrl":"10.1134/S0016702924601554","url":null,"abstract":"<p>The Kaalamo early orogenic Paleoproterozoic massif is located in the southeastern part of the Raahe–Ladoga zone, a junction zone between the Archean Karelian craton and the Proterozoic Svecofennian orogen. The massif consists of three intrusive phases: the first phase is peridotites, olivine clinopyroxenites, and gabbro; the second one is gabbro-norites and gabbro-diorites; and the third phase is diorites, tonalites, and plagiogranites. The paper presents newly obtained data on the petrochemistry and geochemistry of metaperidotites, metapyroxenites, and gabbroids from the Kaalamo complex and on the compositions of their rock-forming minerals. These data were used in the COMAGMAT-3.75 program for thermodynamic calculations of the equilibrium crystallization trajectories of representative rocks and average compositions of the first and second intrusive phases. The calculation results were processed using the geochemical thermometry method, which made it possible to estimate the temperature (∼1220°C) and the probable composition of the initial high-Mg melt (∼9.5 wt % MgO, olivine with 84 mol % forsterite). Comparison of this primitive melt with the model compositions of derivatives and petro- and geochemical characteristics confirms that the rocks of the first and second intrusive phases were derived from a single source, which is consistent with the REE patterns of these rocks and data on their Sm–Nd isotope system and indicate that the rocks have a common mantle source. It was found out that the calculated crystallization sequences of the rocks are in good agreement with the abundance of peridotites and olivine pyroxenites, indicating that the primitive melt was in equilibrium with clinopyroxene and orthopyroxene, which are in peritectic relationships with the olivine. The most differentiated rocks of the first phase are characterized by the crystallization of cotectic plagioclase containing about 80 mol % anorthite. The rocks of the second phase are more differentiated material, corresponding to the gabbronorite association of cumulus phases without olivine and with the late crystallization of titanomagnetite. Comparison of the model and real mineral compositions shows a systematic shift of the natural compositions of the olivine and pyroxenes toward the iron richer from early to late phases, which is a consequence of the interaction of the early cumulus minerals with residual intercumulus melt. The rocks are similar to intrusions of the nickel-bearing belt of Finland, which opens prospects for correlations of magmatic events on an interregional scale.</p>","PeriodicalId":12781,"journal":{"name":"Geochemistry International","volume":"63 3","pages":"209 - 230"},"PeriodicalIF":0.7,"publicationDate":"2025-04-14","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143826615","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"地球科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}

{"title":"Kinetics of Hydrocarbon Formation in the Sedimentary Cover of a Subducting Plate","authors":"D. A. Bushnev","doi":"10.1134/S0016702924601190","DOIUrl":"10.1134/S0016702924601190","url":null,"abstract":"<p>The kinetics of hydrocarbon formation in the sedimentary cover of a subducting plate was numerically simulated using published estimates for the temperature of the subducting plate surface, subsidence rate, and the kinetic spectrum of aquatic organic matter. It was shown that the peak oil window occurs in a subduction environment at depths of 12.6–23.3 km and temperatures of 147.6–179.4°C and requires 0.1–6.4 million years. The scatter in the estimates of depth, temperature, and time required to reach the peak oil window is related to variations in subduction angle and velocity and temperature gradient in the published models. The estimates of depths and temperatures for the formation of hydrocarbons in the sedimentary cover of a subducting plate are higher than those for Cenozoic, Mesozoic, and Paleozoic sedimentary basins, whereas the time required for oil formation is shorter. It can be suggested that accumulations of liquid hydrocarbons could hardly be produced by the organic matter of the sedimentary cover of a subduction plate, but there are prospects for the formation of dry gas fields.</p>","PeriodicalId":12781,"journal":{"name":"Geochemistry International","volume":"63 3","pages":"251 - 258"},"PeriodicalIF":0.7,"publicationDate":"2025-04-14","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143826611","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"地球科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}

{"title":"Thermodynamic Analysis of NixFe1 – x Alloy Oxidation","authors":"V. N. Devyatova,&nbsp;A. G. Simakin,&nbsp;A. N. Nekrasov","doi":"10.1134/S0016702924601621","DOIUrl":"10.1134/S0016702924601621","url":null,"abstract":"<p>This paper reports the thermodynamic analysis of Ni_<i>x</i>Fe_1-<i>x</i> oxidation for awaruite, Ni₃Fe, which is widespread in serpentinized ultrabasic rocks, and other Ni–Fe phases over a wide range of temperatures (400–1873 K) and crustal pressures up to 2 kbar. It was found that the equilibrium γ(Ni_<i>x</i>Fe_{1 –} _<i>x</i>)–Fe oxides constrains oxygen fugacity (<i>f</i>O₂) at the NNO–IW range. For γ(Ni_<i>x</i>Fe_{1 –} _<i>x</i>) with an iron mole fraction <i>x</i> ≥ 0.5, <i>f</i>O₂ approaches the IW buffer. The reaction of kamacite, α(Ni_0.05Fe_0.95), with oxygen is close to the IW–IM buffer reactions. The <i>f</i>O₂ values of awaruite preservation are no higher than ∆QFM = –(7.8–5.2) at <i>T</i> = 400–600 K and increase to ∆QFM = –(2.7–2.0) at <i>T</i> &gt; 1000–1200 K. The obtained approximations of the temperature dependence of <i>f</i>O₂ can be used to estimate the redox conditions in low-sulfide systems containing Ni_<i>x</i>Fe_{1 –} _<i>x</i> under the conditions of the Earth’s crust.</p>","PeriodicalId":12781,"journal":{"name":"Geochemistry International","volume":"63 3","pages":"231 - 241"},"PeriodicalIF":0.7,"publicationDate":"2025-04-14","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143826595","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"地球科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}

{"title":"Compositional Evolution of Calzirtite and Perovskite in Phoscorites and Carbonatites of the Guli Alkaline–Ultramafic Complex, Polar Siberia","authors":"L. N. Kogarko,&nbsp;N. V. Sorokhtina,&nbsp;N. N. Kononkova","doi":"10.1134/S0016702924700885","DOIUrl":"10.1134/S0016702924700885","url":null,"abstract":"<p>The paper presents data on the composition and phase heterogeneity of calzirtite Ca₂Zr₅Ti₂O₁₆ and perovskite CaTiO₃, which are HFSE oxides that crystallized during the early stages of formation of the carbonatite rock series of the Guli alkaline–ultramafic complex in Polar Siberia. The composition of HFSE minerals systematically changed during the evolution of the carbonatite melt from phoscorites to carbonatites. The calzirtite enriched up to 6 wt % Nb₂O₅, and the perovskite enriched up to 15 wt % Nb₂O₅, 7.7 wt % ZrO₂, and 6 wt % LREE₂O₃ in the phoscorites and early calcite carbonatites. Perovskite with low concentrations of admixtures crystallized in the late calcite carbonatites in association with U-, Th-, Ta-rich fluorcalciopyrochlore, thorianite, zirconolite, and baddeleyite. The composition of perovskite-group minerals evolved according to the following of isomorphic exchange schemes: Nb⁵⁺ + Fe³⁺ ↔ Ti⁴⁺ + Zr⁴⁺ and 2Ca²⁺ ↔ Na⁺ + REE³⁺. The enrichment of the early calzirtite and perovskite generations in HFSE is explained by the high Nb, Zr, and LREE partition coefficients in carbonatite melt–mineral equilibria. During the crystallization of the carbonatite melt, the activity of alkaline elements decreased, which is confirmed by a decrease in sodium content in the perovskite and a change in the composition of the solid inclusions. The early generations of perovskite and calzirtite from the phoscorites commonly host numerous polyphase inclusions of Ca, Na, K, Ba, and Sr carbonates, halides, and alkali metal sulfides, whereas calcite, fluorapatite, pyrophanite, and barite are found in the late generations of these minerals. It is shown that the crystallization of the phoscorites have crystallized from anhydrous melt that contained no water, and this was favorable for the preservation of alkaline carbonates as solid inclusions in minerals.</p>","PeriodicalId":12781,"journal":{"name":"Geochemistry International","volume":"63 2","pages":"153 - 171"},"PeriodicalIF":0.7,"publicationDate":"2025-04-04","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143778021","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"地球科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}

{"title":"Standard Thermodynamic Properties of Ag3Sn (Shosanbetsuite): EMF Data","authors":"M. V. Voronin,&nbsp;E. G. Osadchii","doi":"10.1134/S0016702924700861","DOIUrl":"10.1134/S0016702924700861","url":null,"abstract":"<p>Thermodynamic properties of shosanbetsuite (Ag₃Sn) are first determined in the Ag–Sn system in a galvanic cell (–) Pt|Gr|Ag|RbAg₄I₅|Ag₃Sn, Sn|Gr|Pt (+) within the temperature range of 327–427 K in vacuum. Analysis of the data makes it possible to calculate the standard (298.15 K, 10⁵ Pa) Δ_<i>f</i><i>G</i>°, Δ_<i>f</i><i>H</i>°, and <i>S</i>° of Ag₃Sn: –21238, –18763 J mol^–1, and 187.5 J K^–1 mol^–1, respectively.</p>","PeriodicalId":12781,"journal":{"name":"Geochemistry International","volume":"63 2","pages":"183 - 189"},"PeriodicalIF":0.7,"publicationDate":"2025-04-04","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143778057","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"地球科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}