scholarly journals Rare Earth Elements Enrichment in the Upper Eocene Tošići-Dujići Bauxite Deposit, Croatia, and Relation to REE Mineralogy, Parent Material and Weathering Pattern

Minerals ◽  
2021 ◽  
Vol 11 (11) ◽  
pp. 1260
Author(s):  
Nenad Tomašić ◽  
Andrea Čobić ◽  
Matija Bedeković ◽  
Slobodan Miko ◽  
Nikolina Ilijanić ◽  
...  

Tošići-Dujići bauxite deposit, situated in Dalmatian inlands, Croatia, contains minor remaining bauxite reserves. The deposit lies on Lower Eocene foraminiferal limestone and is covered by Upper Eocene Promina sediments. Bauxite samples were analyzed for textural, mineralogical, and geochemical features in order to determine absolute REE abundances and their relation to mineralogy, as well as to devise the origin of REE enrichment and to trace weathering and bauxitization paths of the parent material. The samples show total REE abundances up to 3500 mg/kg with significant HREE enrichment in some cases. All samples are gibbsitic with hematite and anatase as major phases. Kaolinite occurs in most of the samples, and goethite, böhmite, and nordstrandite are minor phases. Monazite-(Ce) and xenotime-(Y) were identified as detrital REE minerals as well as authigenic florencite-(Ce). In the REE most abundant sample, REE are most likely bound to Fe- and Ti-oxide phases as suggested by correlation analysis. Chemical weathering proxies show intensive weathering. Geochemical and textural data imply that the REE enrichment is influenced by intensive weathering (CIA 97.87–99.26) of detrital material, and also by possible deposition/redeposition of residual material potentially derived and mobilized from various sedimentary rocks of the area.

2021 ◽  
Vol 16 (2) ◽  
pp. 123-145
Author(s):  
Vincent Laurent Onana ◽  
Estelle Ndome Effoudou ◽  
Sylvia Desirée Noa Tang ◽  
Véronique Kamgang Kabeyene ◽  
Georges Emmanuel Ekodeck

RésuméUn profil d’altération développé sur chloritoschistes de la zone de Bengbis (Sud Cameroun) a été choisi pour quantifier l’intensité de l’altération et comprendre le comportement des terres rares. Les valeurs de l’indice d’altération mafique combinées aux diagrammes ternaires du système Al – Fe – Mg – Ca – Na – K montrent que l’hydrolyse des feldspaths est proportionnelle à celle des minéraux mafiques (pertes en Mg), bien que l’hydrolyse des plagioclases (Ca, Na) soit plus intense que celle des minéraux ferromagnésiens. Les matériaux d’altération étudiés sont localisés dans le domaine de la kaolinitisation, à l’exception des matériaux nodulaires qui sont légèrement latritiss. La modification du comportement du Mg dans le milieu d’altération s’exprime par les faibles valeurs du rapport Ca/Mg. Le potassium et Be sont lessivés dans le sol en association avec Mg. L’ordre de mobilité des éléments dans l’environnement d’altération étudié est : Ca ≈ Na > Fe2+ ≈ Sr > Mg ≈ Co > Mn > Li > Ba > Rb > P > Cd > Ni > Si > Be > K > Sn. Les enrichissements en K, Cs et Be dans les saprolites sont liés à la présence d’illite. L’accumulation en Cs dans le sol est due à la présence de kaolinite. Le système le plus stable dans le milieu d’altération étudié est : Hf – Nb – W – U. Les saprolites, les matériaux nodulaires et les matériaux argileux meubles superficiels sont appauvris en terres rares par rapport à la roche mère. Les terres rares présentent trois types de comportement le long du profil d’altération, comme l’indiquent les valeurs du rapport (La/Yb)N ((La/Yb)N < 1, (La/Yb)N ~ 1 et (La/Yb)N > 1). Les terres rares légères et les terres rares moyennes s’accumulent dans les matériaux d’altération pour des valeurs de pH comprises entre 5,5 et 5,6 et pour celles de Eh variant entre +60 et +70mV. L’ordre de mobilité de ces éléments dans ces matériaux est le suivant : terres rares moyennes > terres rares lourdes terres rares légères. Ce fait est contre-intuitif, car les terres lourdes sont plus mobiles dans les environnemenst supergènes que les terres rares légères. L’adsorption ou la co-précipitation de ces terres rares sur les oxydes de fer peut principalement contrôler la concentration de ces éléments dans le profil d’altération. Les faibles anomalies en Ce dans les matériaux d’altération de la zone de Bengbis, dues au changement de Ce3+ en Ce4+, sont probablement dues à la présence de faibles quantités de rhabdophane. Les matériaux d’altération étudiés présentent un fractionnement en Gd (Gd/Gd* ~0.70 – 0.84) dues à une intense lixiviation. Ce fait a rarement été signalé dans un environnement d’altération latéritique. Il semble qu’une partie de la distribution et de la remobilisation du gadolinium soit contrôlée par des minéraux mafiques dans les matériaux d’altération étudiés. La distribution et la mobilisation des terres rares sont donc contrôlées par (1) l’adsorption ou la coprécipitation dans les minéraux mafiques et Fe, (2) et légèrement par les minéraux contenant des terres rares tels que le rhabdophane, rencontrés dans les matériaux d’altération étudiés. Abstract An in situ weathering profile overlying chlorite schists in southern Cameroon was chosen to quantify chemical weathering intensity and to study the behaviour of rare earth elements (REE). Mafic index alteration values combined with the ternary diagrams of the Al – Fe – Mg – Ca – Na – K system show that the hydrolysis of feldspars is proportional to that of mafic minerals (losses in Mg), although the hydrolysis of the plagioclases (Ca, Na) is more intense than that of ferromagnesian minerals. The studied materials are localised in the domain of kaolinitisation, except for nodular materials which are slightly lateritised. The change in the behaviour of Mg in the weathering environment is expressed by the low values in Ca/Mg ratio. Potassium and Be are leached in the soil in association with Mg. The order of mobility of the elements in the weathering environment is: Ca ≈  Na > Fe2+ ≈ Sr > Mg ≈ Co > Mn > Li > Ba > Rb > P > Cd > Ni > Si > Be > K > Sn. The enrichments in K, Cs and Be in saprolites are linked to the presence of illite. Cesium accumulation in the soil is due to the presence of kaolinite. The most stable system is: Hf – Nb – W – U. Saprolites, nodular and loose clayey materials are depleted in REE relative to the parent rock. REE exhibit three types of behaviour along the Bengbis profile like indicated by (La/Yb)N ratio values ((La/Yb)N < 1, (La/Yb)N ~ 1 and (La/Yb)N > 1). Light REE and Middle REE accumulate in the weathering materials for pH values ranging between 5.5 and 5.6 and for those of Eh varying between +60 and +70mV. The order of mobility of REE in these horizons is: Middle REE > Heavy REE ≈ Light REE. This fact is counter-intuitive, because Heavy REE are more mobile in supergene environment than Light REE. Adsorption or co-precipitation of LREE onto Fe oxides mainly may control the concentration of these elements in the profile. Weak Ce anomalies in the weathering materials of Bengbis area, due to the change in Ce3+ to Ce4+, are probably due to the presence of low amounts in rhabdophane. The studied weathering materials show a fractionation in Gd (Gd/Gd* ~0.70 – 0.84) due to intense chemical leaching. This fact has been rarely reported in lateritic weathering environment. It appears that, a part of Gd distribution and remobilization is controlled by mafic minerals in the studied weathered materials. REE distribution and mobilization are thus controlled by (1) adsorption or co-precipitation in mafic and Fe minerals, (2) and slightly by REE-bearing minerals such as rhabdophane found in the studied weathering profile.  


Author(s):  
Jan Zalasiewicz

The Earth has the greatest abundance and variety of sedimentary strata in our star system, dating back some 3.8 billion years. ‘Sedimentary rocks’ describes the processes that create different types of sedimentary rocks, which form a key guideline in reconstructing Earth’s history. Particles are created by both physical and chemical weathering. These particles are then moved by different modes of transport and sorted by size, which affect the resulting sedimentary rock. Sedimentary layers can remain as soft muds or loose sands for millions of years, but most buried sedimentary layers harden and turn into rock, under the combined effects of increasing heat and pressure, and of changes in chemical environment.


2020 ◽  
Vol 10 (3) ◽  
pp. 858 ◽  
Author(s):  
Zhang Liankai ◽  
Ji Hongbing ◽  
Wang Shijie ◽  
Luo Gang ◽  
Liu Xiuming ◽  
...  

Research on weathered crusts on carbonate rock is essential for paleoenvironmental studies in karst areas. Terra rossa, widely distributed in tropical karst areas, has not been studied in terms of its material sources and geochemistry. Two typical terra rossa profiles on dolomite (SC profile located at Sang Cai, Hoa Binh province) and limestone (TG profile located at Tong Gia, Lao Cai province) in Northern Vietnam were selected to examine the geochemical characteristics and the evolutionary processes of rare earth elements (REEs). Chondrite and bedrock normalized patterns indicated that these two profiles are in situ weathering crusts, meaning they are the residual material remaining after chemical weathering of the lower carbonate rocks. The average value of total REE in the SC profile is 381.19 ppm, which is 30 times higher than the bedrock. In the TG profile, the value is 386.26 ppm, 13 times higher than the bedrock. Compared with the profiles in nearby subtropical areas in Southeast China, the REE enrichment coefficients of terra rossa in Northern Vietnam are much higher. The REE depletion was also different between the SC and TG profiles. The light and heavy REE fractionations in the SC profile are higher than in the TG profile. Paleoclimate inversion analysis shows that the SC profile experienced a stable oxidation condition, whereas the TG profile was subjected to several reducing environments since a weathering crust formed.


2020 ◽  
Vol 115 (5) ◽  
pp. 1097-1118 ◽  
Author(s):  
Martin Yan Hei Li ◽  
Mei-Fu Zhou ◽  
Anthony E. Williams-Jones

Abstract Subtropical weathering of granitic catchments in South China has led to the formation of numerous giant regolith-hosted rare earth element (REE) deposits that currently account for more than 15% of global REE production and more than 95% of global heavy REE (HREE) production. Understanding the controls on mobilization and redistribution of the REEs during subtropical weathering in these granitic catchments is crucial for efficient exploration for this type of deposit in the world. As exemplified by the Bankeng light REE (LREE) deposit in South China, the key factors controlling the mobilization and redistribution of the REEs, especially the easily exchangeable REEs, are soil pH and primary REE mineralogy. The nature of the primary REE minerals, apatite, monazite-(Ce), and subordinate bastnäsite-(Ce), parisite-(Ce), and xenotime-(Y) places an important control on the behavior of the REEs during incipient weathering. Dissolution of these minerals is slow during incipient weathering, and, therefore, enrichment in REEs in this stage results largely from the removal of major elements during the decomposition of albite, K-feldspar, and biotite. Dissolution of the primary REE minerals higher in the profile liberates the REEs, which are then transported to locations where the soil pH abruptly increases due to water-regolith interaction, such as the pedolith-saprolite interface, and adsorption on kaolinite-group minerals efficiently fixes the REEs in regolith. Geomorphologically, the Bankeng deposit, like most of the other regolith-hosted REE deposits in South China, is located on concave-convex hillslopes, where erosion is prevalent at the ridgetop and decreases in intensity downslope. Results of this study show that strong erosion, coupled with intense chemical weathering at the ridgetop, is responsible for the enrichment in REEs by releasing the REEs, especially the LREEs, from their primary sources and supplying kaolinite and halloysite needed for the REE adsorption by decomposing albite, K-feldspar, and biotite. Decomposition of these major rock-forming minerals also leads to an enrichment of the REEs through the removal of components. The HREEs are lost preferentially to the groundwater and transported downslope, resulting in the enrichment of these elements in the lower part of the weathering crust at the footslope. Significant lateral Ce transport is also probable. A series of oxic fronts were developed at the footslope, with the most persistent one along the saprolite-saprock interface, due to seasonal fluctuations of the groundwater table. Cerium was immobilized there, predominantly through adsorption on Fe-Mn oxyhydroxides, causing enormous accumulation. Therefore, hillslope processes and groundwater flow could redistribute the REEs across the entire catchment, preferentially enriching the LREEs at the ridgetop and the HREEs at the footslope. Also, intense erosion facilitates chemical weathering and the accumulation of REEs, but the development of a thick weathering crust is favored by weak erosion. Repeated periods of high and low erosion rates in South China have enabled the gradual development of thick weathering crusts at the ridgetops that are sufficiently enriched in REEs to now constitute a major resource of these economically important elements.


1963 ◽  
Vol S7-V (5) ◽  
pp. 782-789 ◽  
Author(s):  
Jean Paul Rampnoux

Abstract The NE-SW trending Stivo-Cornetto anticline (Trento province) forms a line of crests separating the Sarca valley from the Adige river valley. The entirely marine sequence includes Liassic and Dogger subreefal limestones succeeded by Malm, Cretaceous and lower Eocene deep water deposits. Emergence or regression resulted in the deposition of neritic facies during the middle and upper Eocene and the Oligocene and Miocene. The deposits are representative of the Tridentine zone.


2019 ◽  
Vol 520 ◽  
pp. 33-51 ◽  
Author(s):  
Wei Fu ◽  
Xiaoting Li ◽  
Yangyang Feng ◽  
Meng Feng ◽  
Zhao Peng ◽  
...  

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