Rare Earth Element Geochemistry Research Articles

Rare-earth elements geochemistry of the Palaeocene Ewekoro Formation, southwestern Nigeria: implications for terrigenous inputs, diagenetic alteration, palaeoredox and depositional conditions

Rare-earth elements geochemistry of the Palaeocene Ewekoro Formation, southwestern Nigeria: implications for terrigenous inputs, diagenetic alteration, palaeoredox and depositional conditions

Drivers of rare earth elements (REEs) and radionuclides in changing subarctic (Nunavik, Canada) surface waters near a mining project

The emergence of mining projects for rare earth elements (REEs) in response to rising global demand and geopolitical factors introduces environmental concerns, such as the suspected release of anthropogenic REEs to aquatic systems and the coexistence of radionuclides (U, Th). Northern regions confront heightened challenges from limited research and accelerated climate change. Drivers of REEs in surface waters (including George and Koroc rivers, their tributaries, and thermokarst lakes) were studied (2017–2023) in subarctic Canada within a climate transition zone, near a prospective REE mine. Dissolved REEs (<0.45 μm) correlated positively with Al, Fe, Th, U, Cl– and DOC. A novel relationship with water temperature demonstrated an approximate 10-fold decrease in REE concentrations over the environmental gradient (2–20 ℃), suggesting complex implications for REE speciation under climate pressures. Optical analyses further predicted REEs were mobilized by humic-rich, terrestrial DOC, with correlations presenting a possible co-transport with Al, Fe and Th. Relationships for redox-sensitive Ce anomalies (Ce/Ce* = 0.18–1.2) with multi-valent trace metals (Al, Fe, Ti) and DOC were suggestive of a preferential adsorption of Ce by inorganic colloids in low-DOC systems. Findings emphasized the potential for changes in REE geochemistry with ongoing northern surface warming and vegetation shifts.

Features of rare earth elements geochemistry in coals of Central Kazakhstan

AbstractThis research presents the results of a comprehensive study of mineralogical and geochemical features of REE distribution in coals of Central Kazakhstan deposits—Karaganda coal basin and Shubarkol deposit, which have large hard coal reserves and are industrially important for the coal industry of Kazakhstan; the research is based on 205 samples of clayey interlayers and coal seams. It shows basic patterns of distribution and features of concentration for impurity elements, gives an estimate of the impurity elements concentration, including REE, defines conditions and factors of their accumulation, and studies features of their forms in coal and coal-bearing rocks, which allows estimating the mechanisms of their migration and conditions of accumulation. According to the results of geochemical indicators, the article establishes the factors of REE dislocation, reveals the composition of margin rocks that have influenced REE concentration in coal seams, and the presented latest data on mineralogy allowed to establish the ways of their transportation to the paleobasin during the syn- and epigenetic periods of formation of the coal deposits of Central Kazakhstan being researched. It was found that the coals are insignificantly enriched with heavy lanthanides from Ho to Lu. The distribution curves of UCC normalized REE values in the coals are similar and coincide, but they are less than the average value for world coal, and amount to only one-third of the UCC. It was found that the highest concentrations of all REE are characteristic of clayey interlayers and oxidized coals. The La/Yb ratio in this case increases upwards along the section, indicating mainly clastogenic mechanism of REE delivery to the coals. In coal and clay samples, the predominant mineral form of REE is light lanthanide phosphates. Identified particles of REE from minerals and their composition peculiarities suppose autigene nature of their formation. The formation of the bulk of autigene minerals occurred during the maturation of brown coals and their transformation into hard ones.

Rare earth element geochemistry of reef carbonates in the South China Sea since the Miocene: Insights into paleoclimatic significance

Seawater chemistry critically affects the functioning of ocean ecosystems. However, the evolution of the seawater chemistry in the South China Sea (SCS) since the Miocene is not fully resolved, and its links to tectonic and climate changes remain unclear. In-situ, shallow marine carbonates can provide insights into long-term changes in seawater chemistry and associated environmental processes. In this study, we conducted the rare earth element (REE) analysis of the NK-1 core in the southern SCS since the Miocene. The results reveal poor relationships between siliciclastic/diagenetic indicators (mineralogical, isotopic, and elemental data) and REE proxies, which demonstrate that the REE compositions are insensitive to non-carbonate contaminations and diagenesis. The results exhibit seawater-like REE patterns with LREE depletion, positive La anomaly, superchondritic Y/Ho ratio, and negative Ce anomaly, which demonstrate that this core has preserved a signal of the primary seawater REE composition. The Y/Ho ratios range from 45 to 80 and La anomalies range from 1.0 to 2.3 during ∼23–13 Ma, and they then decrease after ∼13 Ma, with the Y/Ho ratios ranging from 30 to 52 and La anomalies ranging from 0.6 to 1.5. Considering that seawater REE components are mainly sourced from terrigenous sources which exhibit lower La anomalies and Y/Ho ratios, our results indicate an enhanced terrigenous input since ∼13 Ma. We consider that the climate cooling and aridity since ∼13 Ma might be responsible for the phenomenon.

Integrated photogrammetry, lava geochemistry and palynological re-evaluation of the early evolution of the topographically constrained Mull Lava Field, Scotland

ABSTRACT Photogrammetry was used to elucidate complex strata relationships between isolated outcrops of the Palaeocene lava fields of SW Mull, part of the North Atlantic Igneous Province. Subsequent sampling for lava geochemistry and palynology was undertaken based on interpretation of these photogrammetry models. Coherent units of Plateau- and Staffa-type lavas were identified using lava geochemistry, in particular using rare earth elements (REEs), divisions supported by multivariate statistics. Lavas with three different REE compositional clusters were identified within the Staffa magma type and four within the Plateau type of SW Mull. Understanding the distribution of these lava types was achieved using the interpreted photogrammetry models and analysis of prominent interbedded sedimentary rock units and their correlative unconformities. Probably the most renowned rocks of SW Mull are the thick columnar jointed lavas, including those of the Isle of Staffa. REE geochemistry reveals that lavas of both Staffa- and Plateau-type geochemistry occur as columnar jointed facies associated with what has previously been attributed to the Staffa Lava Formation. Instead, the SW Mull Lava Field was initiated by eruption of Plateau-type lava into a fault-controlled valley. Subsequent eruptions of Staffa-type lavas partially infilled this structure, which was finally overfilled by a thick succession of younger Plateau-type lavas. The geochemical characteristics of this Plateau–Staffa–Plateau lava succession indicate that magma reservoirs deep in the crust were succeeded by shallow melts during a period of crustal extension. This phase of shallow melting induced topographical instability and formation of sedimentary interbeds and correlative unconformities that characterise the Staffa-type lava succession. Subsequent compressive tectonics forced a return to deep crustal melts. Interbed palynofloral compositional data indicate that eruption of the later Plateau-type lavas likely took place within a period of ~2.5 million years during the Selandian to early Thanetian period.

Geochemistry of Rare Earth Elements in Pahang River Sediment, Malaysia

Rare earth elements (REE) are a set of 17 chemically similar metallic elements including 15 lanthanides, scandium and yttrium. The current status of REE as a global strategic commodity has encouraged the identification of REE ore deposits. This research is carried out to identify the mining feasibility of fluvial sediment REE and to understand the sediment's physical and chemical characteristics and effects on the geochemical behaviour of REE in the longest river of Peninsular Malaysia namely Pahang River. Surface sediment samples were collected along Pahang River (n=44) in approximately 10 km distance intervals. The sediment samples were analyzed using XRF to determine the major oxide content. Meanwhile, REE content in the sediment samples was extracted using the Total Digestion method and analysed using ICP-MS. The results show the average value of ΣREE at surface sediments of the Pahang River is 42.58 ppm and can be considered too low to be economically mined. Each area shows higher fractionation of light REE than heavy REE with negative europium anomalies, suggesting sediments in this area were derived from felsic rocks. The concentration of REE in Pahang River surface sediments was controlled by the porosity and organic matter as showed by the correlation of ΣREE with porosity (R2=0.65) and organic matter content (R2=0.71). In conclusion, this research's findings are generally useful for further REE mineral exploration and fluvial sediment environmental monitoring.

Rare earth element behaviors of groundwater in overlying aquifers under the influence of coal mining in northern Ordos Basin, China.

Rare earth elements (REEs) have been used as tracers to reveal the hydrochemical sources and processes in groundwater systems that are usually modified by anthropogenic inputs. However, the REE behaviors in groundwater affected by mining activities have yet to be fully understood. In combination of REE geochemistry with general hydrochemical and isotopic (δ2H and δ18O) methods, this study investigated the concentration and fractionation of REEs in alkaline groundwater from two coal mines with similar aquifer lithology but different mining histories in the Northern Ordos Basin. One of the coal mines started mining in March 2009 (Ningtiaota coal mine, NTT), while the other started mining in December 2018 (Caojiatan coal mine, CJT). Results show that the primary hydrochemical type is HCO3-Ca in NTT groundwater with pH value ranging between 7.68 and 8.60, while CJT groundwater was dominated by the HCO3-Na type with higher pH of 9.09-10.00. The average values of ΣREEs were lower, and the NASC-normalized pattern reflected more intense fractionation in NTT groundwater than those in CJT groundwater. The evident differences are caused by the distinctions in water-rock interaction, complexation of inorganic species, and adsorption of REEs in NTT and CJT groundwater. Furthermore, these processes were closely related to the pH of groundwater that was different in two coal mines, which is likely linked to the different durations of coal mining activities that led to differences in development of rock fractures and pyrite oxidation. It is expected that REEs, combined with other indicators such as pH, can be used to trace and help better understand the hydrochemical changes in groundwater caused by mining.

Geochemical evaluation of the genetic relationship of Kısacık (Ayvacık, Çanakkale/Türkiye) epithermal gold mineralization using trace and rare earth elements

The Kısacık gold deposit is situated in the Biga Peninsula, Northwest Anatolia, Türkiye. The aim of this study is to investigate the genetic relationship between the Kısacık gold deposit and the surrounding rocks using trace element and rare earth element (REE) geochemistry. The results show that the gold mineralizations in the Kısacık area have a compatible pattern with the Alakeçi-Kısacık Volcanics and the Kuşçayırı plutonic rocks in the near vicinity of the area. The gold mineralizations in the Kısacık area are consistent with the trace and rare earth element (REE) patterns of the upper continental and lower continental crust, as shown by comparison with spider diagrams normalized to different geological settings. The gold enrichments in the listvenites and ultramafic rocks in the area are also consistent with the trace and REE element patterns of these rock types. The results of this study support the conclusion that the gold mineralization in the Kısacık area is related to hydrothermal fluids that leached elements from the Alakeçi-Kısacık Volcanics. In addition, hydrothermal fluids from plutonic rocks were also effective in the mineralization process. These results suggest that the gold mineralization in the Kısacık area is related to hydrothermal fluids that leached elements from the Alakeçi-Kısacık Volcanics.

Geochemical and Isotopic Compositions of Fluorites from the Yama Fluorite Deposit in the Qilian Orogen in Northwest China, and Their Metallogenic Implications

The Yama area is characterized by numerous large-scale fluorite–quartz veins that are located along faults within the widespread Late Devonian–Late Silurian syenogranites in the Tataleng granitic batholith, Qilian Orogen, Northwest China. These fluorite–quartz veins contribute to an important fluorite reserve, but their ore genesis remains unresolved so far. In this study, trace elements, rare earth elements (REEs), and hydrogen, oxygen, and strontium isotopic compositions of fluorites are analyzed. The studied fluorite samples have similar chondrite-normalized REEs, including Y patterns, with relatively strong enrichment in heavy REEs, negative Eu anomalies, strongly positive Y anomalies, and comparably invariable Y/Ho ratios of 41.43–73.79, suggesting a unique hydrothermal genesis. The relatively variable values of δD and δ18O are −77.4‰ to −102.4‰ and −12.7‰ to −4.3‰, respectively, close to the meteoric water line. These fluorites yield relatively invariable analytical 87Sr/86Sr ratios of 0.749089−0.756628 (except for an anomalously high ratio), and their calculated initial 87Sr/86Sr ratios, based on the ore-forming ages provided, are apparently higher than the calculated initial 87Sr/86Sr ratios of syenogranite wall rocks. Collectively, the geochemistry of trace elements, REEs, and stable isotopes (H, O, and Sr) suggests that the ore-forming fluids were of meteoric origin and that the Sr sources were directly derived from the ore-forming fluids themselves rather than syenogranite wall rocks. Finally, it was considered that the Yama fluorite deposit is a fault-controlled hydrothermal vein-type deposit which was possibly related to the evolution of the Paleo-Tethys Ocean in the Permian–Triassic.

Геохимия редкоземельных элементов и цериевая аномалия в морских осадочных карбонатах: современные представления

The article review the geochemistry of rare earth elements (REE) in sedimentary marine carbonates (limestones and dolostones) with respect to using the cerium anomaly as a proxy for redox conditions in ancient seawater. The physicochemical properties of REE and Y, the problem of normalizing their contents in sediments, behavior in the World Ocean and in chemogenic deposits, the origin of La, Ce, Eu, Gd anomalies and their calculations, sample preparation techniques, contamination problem and the influence of non-carbonate REE+Y-hosting phases to whole rock and acidic leachate compositions, as well as criteria for determining seawater-like pattern are considered.

Provenance and depositional setting of the Late Miocene- Pleistocene clastic sediments in the eastern Arabian Peninsula and western Iraq using rare earth elements geochemistry

Provenance and depositional setting of the Late Miocene- Pleistocene clastic sediments in the eastern Arabian Peninsula and western Iraq using rare earth elements geochemistry

REE distribution and enrichment of drainage point sediments from Makran and Lasbela, Pakistan

Rare Earth Elements (REEs) are mobile during weathering and their distribution is susceptible to both natural and anthropogenic influences. Four major drainage points in the Makran and Lasbela areas were selected for sampling to examine their REE geochemistry. The mean values of ∑REE are highest in Dasht River (DR: 109.4) and lowest in Shadi River (SR: 84.4). The mean values of Eu/Eu* are highest in Rakhshan River (RR:0.95) and lowest in DR (0.70); these values are higher as compared to the Upper Continental Crust (UCC: 0.23) and Post-Archean Australian shale (PAAS: 0.21) in all drainage points. The mean values of (Gd/Yb)N are highest in RR (2.66) and lowest in DR (2.03), while the mean values of Ce/Ce*, (La/Sm)N, (La/Yb)N, and (La/Lu)N are highest in DR (1.01, 3.01, 9.86 and 9.66, respectively) and lowest in RR (0.93, 1.49, 5.75 and 5.93). DR and HR, covering the longest distances from headwater to mouth, pass through a variety of lithologies and convey a more diverse range of sediment compared to RR and SR. Noticeably depleted elemental concentrations relative to UCC (elemental ratios <1) are observed in the majority of sediments, implying the influence of weathered source rocks. Normalized chondrite distributions of the REEs exhibit consistent trends marked by an enrichment of LREEs and a depletion of HREEs, a characteristic pattern was found in upper crust materials exposed to weathering and erosion. The presence of a positive Eu anomaly in UCC and PAAS normalized patterns suggests the contribution of plagioclase minerals. However, leaching is insignificant for the studied sediments due to low average annual precipitation.

Determination of Rare Earth Element Isotopic Compositions Using Sample-Standard Bracketing and Double-Spike Approaches.

Rare earth elements (REEs) have been found to have numerous uses to trace geological and cosmochemical processes through analyses of elemental patterns, radioactive decay, nucleosynthetic anomalies, and cosmogenic effects. Stable isotopic fractionation is one aspect of REE geochemistry that has been seldom studied, with most publications focusing on the development of analytical methodologies for individual REEs, and most applications concerning terrestrial igneous rocks. In this study, we present a method to systematically analyze stable isotopic fractionations of 8 REEs, including Ce, Nd, Sm, Eu, Gd, Dy, Er, and Yb, using sample-standard bracketing (SSB) and double-spike (DS) approaches. All REEs are separated and purified using a fluoropolymer pneumatic liquid chromatography (FPLC) system. We introduce procedures for identifying and correcting some isobaric interferences in double-spike data reduction. Several geostandards, including igneous rocks and sediments, are analyzed using SSB and DS methods. The results indicate that REE isotopic fractionation in igneous processes is limited, except for Eu. Other REEs can still be isotopically fractionated by low-temperature processes and kinetic effects at a high temperature.

Geochemistry of rare earth and trace elements in springs and surface water in the Havza (Samsun) area, NE Turkey

Geochemistry of rare earth and trace elements in springs and surface water in the Havza (Samsun) area, NE Turkey

Persistent late Tonian shallow marine anoxia and euxinia

The increase in the complexity of eukaryotic life during the Tonian Period (ca. 1000 to 720 Ma) is commonly associated with the oxygenation of the Earth’s ocean–atmosphere system, yet the timing and duration of these redox changes remain uncertain. In particular, it is unclear how shallow marine environments, which were likely crucial habitats for early eukaryotic organisms, responded to Neoproterozoic oxygenation. This study uses trace and rare earth element geochemistry to determine shallow marine redox conditions during the deposition of the late Tonian (ca. 760 Ma) Devede Formation, northern Namibia. In this unit, although carbonate phases (microbialite, former aragonite and high Mg calcite marine cements, and primary dolomite marine cements) generally exhibit no Ce/Ce* anomaly, rare negative values (up to 0.55) are consistent with short-lived periods of oxygenation. In contrast, the dominantly positive Eu/Eu* anomalies of the same phases suggest that basinal conditions were anoxic. These phases also exhibit low concentrations of redox-sensitive (U, V, Mo) and chalcophile (Co, Cu, Cd, Zn, Pb) elements, suggesting that euxinic conditions were predominant during the deposition of the Devede Formation. Integration of this data (Ce/Ce* and Eu/Eu*) with that of analogous late Tonian (ca. 840 to 731 Ma) carbonate strata reveals that shallow marine settings were characterised by persistent anoxia and euxinia, suggesting that any potential increase in atmospheric O2 ca. 800 Ma (e.g. the Bitter Springs Anomaly) was insufficient to facilitate resilient ocean oxygenation. These findings suggest that the late Tonian oceans were likely challenging environments for complex (e.g. eukaryotic) life, and add to a growing body of evidence that the spatially variable redox conditions of late Proterozoic shallow marine settings likely reflect the complex nature of the Neoproterozoic Oxygenation Event.

Lead isotopes and rare earth elements geochemistry of global phosphate rocks: Insights into depositional conditions and environmental tracing

Phosphate rock bears both geologically and environmentally significant information. Rare earth elements and yttrium (i.e., REY) characteristics have been commonly used for reconstructing the redox conditions of depositional environments and the effects of post-depositional diagenetic alteration on phosphate rock. In addition, phosphate rock is typically enriched in a range of trace elements such as uranium (U) and cadium (Cd) that can be dispersed as contaminants into the environment with phosphate mining and phosphate fertilizer application. Here we report the lead (Pb) isotope compositions combined with Pb and REY concentrations of both global sedimentary and igneous phosphate rocks, aiming to evalute the geological origin of phosphate rocks over time and the potential of using them for environmental tracing. Phopshate rock samples analyzed in this study were sourced from major economic phosphate deposits in the world, including China, Southern Tethys (e.g., Morocco, Tunisia, Israel), the U.S., India, South Africa and Russia. Our results show a wide range of 208Pb/204Pb (35.70 to 60.58), 207Pb/204Pb (15.20 to 18.25), and 206Pb/204Pb (16.369 to 71.806) ratios in the phosphate rocks, with sedimentary phosphate rocks being significantly more radiogenic than igneous rocks. The majority of sedimentray phosphate rocks show a notable isotopic overprinting by non-radiogenic terrestrial Pb, except for those from Israel and Morocco that have the most radiogenic Pb isotope compositions. Correspondingly, phosphate rocks with more radiogenic Pb isotope ratios show relatively pristine seawater REY features, likely suggesting their preservation of the original oxic seawater conditions and/or minimal diagenetic alteration. In contrast, phosphate rocks with less radiogenic Pb isotope compositions show REY indications for more anoxic seawater redox conditions and/or greater diagenetic alteration. We further evaluate the potential utility of Pb isotopes for tracing the associated contamination with phosphate rock mining and fertilizer application in the environment. In most cases, the radiogenic Pb isotope composition of phosphate rocks and corresponding P-fertilizers is distinctive from both natural crustal Pb and major anthropogenic Pb sources (e.g., Pb ore deposits and pesticides), which provides a great advantage for applying Pb isotopes as an environmental tracer for metal(loid) contamination from phosphate sources. The combination of Pb isotope ratios and REY proxies could further constrain the Pb source discrimination. Overall, this study provides new Pb isotopic and REY geochemical data on global phosphate rocks and fertilizers, which lays the groundwork for future regional and local studies on both their geological and environmental implications.

Trace and Rare Earth Elements Geochemistry of the Mudstone Rocks from the Injana Formation: Implications for Provenance and Paleoclimate

Late Miocene-Pliocene mudstones of the Injana Formation were examined to provide insight into the nature of the source rocks and paleoclimate. For these purposes, 23 mudstone samples from three locations Mirawa and Degala in the Erbil, northern Iraq and Najaf from southern Iraq. These samples were analyzed by ICP-MS to measure the concentrations of the trace and rare-earth elements (REE). The chondrite-normalized REE of all samples are similar and shows slight enrichment with LREE relative to the HREE with negligible negative Eu anomaly. The discriminant plots of the trace elements and the enrichment factors suggest that the source was intermediate-mafic rocks, and the climate was warm and humid during the deposition of the mudstone of the Injana Formation.

The youngest lunar zircon reveals an extremely fractionated nature of Chang’e-5 basalt

The U(Pb)-Pb age of zircon is commonly used to represent the crystallization age for igneous rocks due to its high closure temperature and robust resistance to impact disturbance. However, no zircon crystallization age has yet been reported for Chang'e-5 (CE-5) basalt due to their limited occurrence in mare basalt. In this study, rare zircon grains from CE-5 lunar samples were investigated by the in-situ Pb isotopic analysis, and a precise zircon crystallization age of 2036 ± 19 Ma was determined from Pb-Pb isochron. This is hitherto the youngest reported crystallization age of lunar zircon, similar to the ages of CE-5 lunar basalts obtained by zirconium (Zr)-bearing minerals such as baddeleyite, tranquillityite, and zirconolite. Petrographic evidence and rare-earth element geochemistry indicate that zircon in the CE-5 lunar basalts were formed by the reaction of early-formed baddeleyite with SiO2 melt within the latest residue of extreme fractionation of a non-KREEP (an acronym for potassium, REE, and phosphorus) basaltic magma. In contrast to the prevailing view that lunar zircon have formed in late-stage enriched melts resulting from extensive fractional crystallization of the Lunar Magma Ocean, this study shows that zircon could be derived from extreme fractionation of non-KREEP basaltic magma unrelated to Lunar Magma Ocean.

Geology and Rare Earth Element Geochemistry of Magnesian Granitoids Within Proterozoic Schist Belt of Southwest Nigeria

Abstract The increased global demand for and price of rare earth elements (REEs) has led to intensive search for them in rocks of the upper continental crust all over the world. This study is aimed at characterising the granitoids at Okeho within Southwestern Nigeria using geochemical data and assessing their potential for REE enrichment. Ten representative rock samples of the Proterozoic intrusives, syenite and granodiorite, were studied for their mineralogical and elemental compositions. Elemental concentrations were analysed using Inductively Coupled Plasma Mass Spectrometry (ICP-MS). Average major oxide concentrations revealed SiO2 (57.53 wt. %), Al2O3 (13.25 wt. %), CaO (5.05 wt. %), and MgO (5.59 wt. %) for the syenite and SiO2 (62.39 wt. %), Al2O3 (14.98 wt. %), CaO (3.67 wt. %), and MgO (3.25 wt. %) for the granodiorite. Total Alkali–Silica (TAS), Aluminum Saturation Index (ASI), and La/10-Y/15-Nb/8 plots discriminated the granitoids as metaluminous monzonite-syenite and peraluminous diorite-granodiorite. Average total REE concentrations in the syenite (625.06 ppm) and porphyritic-granodiorite (364.51 ppm) were above values reported for the granites in some mines in Jiangxi Province, Southern China.

Geochemistry and Mineralogy of Rare-Earth Elements in Ferruginous Deposits and Bottom Sediments of the Laptev Sea

Abstract —The geochemical and mineralogical aspects of the distribution of rare-earth elements (REE) in ferruginous deposits (FD) and bottom sediments of the southeastern Laptev Sea are analyzed. The FD are dominated by biomorphs developed after polychaete tubes. The REE patterns depend on the proportion of ore and non-ore substances. The ore substance is represented mainly by iron hydroxides (limonite). It is a product of suboxic diagenesis enhanced by bioturbation and determines the slight enrichment of FD in MREE and cerium deficiency (Cean = 0.94). The non-ore substance comes from terrigenous sediments and has an (alumino)silicate composition. It controls the scandium content and is the source of REE mineral grains, among which monazite-(Ce) prevails. The sediments demonstrate a common similarity in REE patterns to shales and suspended material transported to the Laptev Sea by the Lena River, with elevated LREE and MREE contents and the value of Ce anomaly almost equal to unity (Cean = 1.06). In the sediments, REE minerals occur mostly in the silt fraction (&amp;lt;63 μm in size). The high content of organic matter (Corg of up to 2.15%) of predominantly terrigenous origin (OMter of up to 85%) in the sediments explains the oxygen deficiency and weak diagenetic mineral formation with low accumulation of trace elements, including REE, in the FD. The total REE content in the FD is lower than that in the sediments (on average, 173 ppm against 206 ppm).