Genesis of Late Miocene-Pliocene lacustrine palygorskite and calcretes from Kırşehir, central Anatolia, Turkey

Clay Minerals ◽  
2014 ◽  
Vol 49 (3) ◽  
pp. 473-494 ◽  
Author(s):  
S. Kadİr ◽  
M. Eren ◽  
T. Külah ◽  
N. Önalgİl ◽  
M. Cesur ◽  
...  

AbstractThis paper addresses the mineralogy, geochemistry, and genesis of palygorskite and associated calcretes in the Kırşehir region. In this area, the Quaternary calcretes are present within and/or on lacustrine mudstones of the Kızılırmak Formation (Late Miocene-Pliocene). The calcretes occur in the form of nodules, tubes, fracture-infills, and hard laminated crusts (hardpans). Calcrete samples are predominantly composed of calcite associated with smectite, quartz, feldspar, and minor palygorskite. The lacustrine mudstone samples consist mainly of smectite and palygorskite with minor calcite, quartz, feldspar, illite, kaolinite and amorphous material. Petrographic studies revealed that the calcrete samples are predominantly micrites that were partially converted to microsparites by recrystallization. Scanning and transmission electron microscopy images indicate that palygorskite fibres formed authigenically on and between calcite rhombs in the calcrete samples and at the edges of smectite flakes of host rocks adjacent to the calcretes. The oxygen and hydrogen stable isotope values of the calcite suggest that it precipitated from meteoric water under arid or seasonally arid climatic conditions. Calcite precipitation occurred in the vadose zone, as evidenced by desiccation cracks and vadose pisolites. The enrichment of Rb+Ba±Sr and Light Rare Earth Elements (LREE) relative to Heavy Rare Earth Elements (HREE)with a distinct negative Eu anomaly are responses to the fractionation of volcanogenic feldspar and hornblende under the influence of meteoric water. The palygorskite associated with calcretes was precipitated from alkaline water rich in Si, Al and Fe and low in Mg. The palygorskite precipitation occurred at increased temperatures, characterising the advanced stage of calcrete formation which lowers the Ca content in the soil water. The required chemical elements for palygorskite and calcite were most likely derived from the dissolution of smectitic clays, ignimbrites and carbonate minerals.

2021 ◽  
Vol 59 (5) ◽  
pp. 985-1019
Author(s):  
Nicholas Joyce ◽  
Daniel Layton-Matthews ◽  
Kurt Kyser ◽  
Matthew Leybourne ◽  
Kevin Ansdell ◽  
...  

ABSTRACT Pathfinder elements associated with the exploration footprint of the McArthur River unconformity-related U deposit include U, radiogenic Pb, V, Ni, Co, Cu, Mo, As, Zn, and rare earth elements. In this study, the mineralogical and paragenetic context for their occurrence was established by integrating in situ mineral chemistry and laser ablation mass spectrometry chemical mapping of interstitial assemblages, detrital grains, and cements with whole-rock analyses of drill core samples from the diagenetically altered background and the hydrothermally altered sandstone host rocks. Diagenetically altered background sandstones contain a matrix assemblage of illite and dickite, with trace to minor aluminum-phosphate-sulfate (APS) minerals, apatite, and Fe-Ti oxide minerals. Aluminum-phosphate-sulfate minerals account for the majority of the Sr and light rare earth element concentrations, whereas early diagenetic apatite, monazite, and apatite inclusions in detrital quartz and detrital zircon contribute significant U and heavy rare earth elements to samples analyzed with an aggressive leach (partial digestion) such as aqua regia. Hydrothermally altered sandstone host rocks also contain variable assemblages of Al-Mg chlorite (sudoite), alkali-deficient tourmaline, APS minerals, kaolinite, illite, Fe-oxide, and sulfide minerals. Late pre-mineralization chlorite accounts for a significant portion of the observed Ni concentrations, whereas Co, Cu, Mo, and Zn occur predominantly in cryptic sub-micron sulfide and sulfarsenide inclusions within clay mineral aggregates and in association with Fe-Ti oxides. Elevated concentrations of U were observed in cryptic micro-inclusions associated with sulfides in quartz overgrowths, with Fe-Ti oxide micro-inclusions in kaolinite, and in post-mineralization Fe-oxide veins. The distribution of pathfinder elements throughout the deposit footprint appears to be less related to the primary dispersion of alteration minerals from the hydrothermal system than to the secondary dispersion of elements post-mineralization. Their occurrence throughout pre-, syn-, and post-mineralization assemblages further demonstrates the limitations to defining geochemical footprints from pathfinder element concentrations expressed in lithogeochemical data sets without structural, lithological, and mineralogical context.


Minerals ◽  
2021 ◽  
Vol 11 (8) ◽  
pp. 802
Author(s):  
Lorena Hernández-Filiberto ◽  
Encarnación Roda-Robles ◽  
William B. Simmons ◽  
Karen L. Webber

Almandine-spessartine garnets, from the Oxford County pegmatites and the Palermo No. 1 pegmatite, record significant compositional variations according to the degree of evolution of their hosting rock. Garnets from the most fractionated pegmatites (Mt. Mica, Berry-Havey, and Emmons) show the highest Mn, Nb, Ta, Zr, and Hf values, followed by those from the intermediate grade pegmatites (Palermo No. 1) and, finally, garnets from the barren pegmatites show the lowest values (Perham and Stop-35). Iron, Ca, and Mg contents follow an inverse order, with the highest contents in the latter pegmatites. Major element zoning shows increasing Mn values from core to rim in most garnet samples, while trace element zoning is not systematic except for some crystals which show a core to rim depletion for most of these elements. Chondrite normalized HREE (Heavy Rare Earth Elements) spectra show positive slopes for garnets from barren pegmatites, both positive and negative slopes for those associated with the intermediate pegmatite, and negative or flat slopes in garnets from the highly fractionated pegmatites. Ion exchange mechanisms, including Fe2+−1Mn2+1, (Fe2+, Mn2+)−1Si−1Li1P1; and, (Y, Ho3+)2(vac)1(Fe2+, Mn2+)−3, could explain most of the compositional variations observed in these garnets. These compositional variations are the reflection of the composition of the pegmatitic magma (barren pegmatites originate from a more ferromagnesian magma than fractionated pegmatites); and of the coexisting mineral phases competing with garnets to host certain chemical elements, such as biotite, schorl, plagioclase, apatite, Fe-Mn phosphates, Nb-Ta oxides, zircon, xenotime, and monazite.


2021 ◽  
Vol 6 (1) ◽  
Author(s):  
Anna Galler ◽  
Semih Ener ◽  
Fernando Maccari ◽  
Imants Dirba ◽  
Konstantin P. Skokov ◽  
...  

AbstractCerium-based intermetallics are currently attracting much interest as a possible alternative to existing high-performance magnets containing scarce heavy rare-earth elements. However, the intrinsic magnetic properties of Ce in these systems are poorly understood due to the difficulty of a quantitative description of the Kondo effect, a many-body phenomenon where conduction electrons screen out the Ce-4f moment. Here, we show that the Ce-4f shell in Ce–Fe intermetallics is partially Kondo screened. The Kondo scale is dramatically enhanced by nitrogen interstitials suppressing the Ce-4f contribution to the magnetic anisotropy, in striking contrast to the effect of nitrogenation in isostructural intermetallics containing other rare-earth elements. We determine the full temperature dependence of the Ce-4f single-ion anisotropy and show that even unscreened Ce-4f moments contribute little to the room-temperature intrinsic magnetic hardness. Our study thus establishes fundamental constraints on the potential of cerium-based permanent magnet intermetallics.


2016 ◽  
Vol 159 ◽  
pp. 157-160 ◽  
Author(s):  
Takeshi Ogata ◽  
Hirokazu Narita ◽  
Mikiya Tanaka ◽  
Mihoko Hoshino ◽  
Yoshiaki Kon ◽  
...  

2021 ◽  
pp. 1-41
Author(s):  
Lianfu Hai ◽  
Qinghai Xu ◽  
Caixia Mu ◽  
Rui Tao ◽  
Lei Wang ◽  
...  

In the Tanshan area, which is at the Liupanshui Basin, abundant oil shale resources are associated with coals. We analyzed the cores, geochemistry of rare earth elements (REE) and trace element of oil shale with ICP-MS technology to define the palaeo-sedimentary environment, material source and geological significance of oil shale in this area. The results of the summed compositions of REE, and the total REE contents (SREE), in the Yan'an Formation oil shale are slightly higher than the global average of the composition of the upper continental crustal (UCC) and are lower than that of North American shales. The REE distribution pattern is characterized by right-inclined enrichment of light rare earth elements (LREE) and relative loss of heavy rare earth elements (HREE), which reflects the characteristics of crustal source deposition. There is a moderate degree of differentiation among LREE, while the differences among HREE are not obvious. The dEu values show a weak negative anomaly and the dCe values show no anomaly, which are generally consistent with the distribution of REE in the upper crust. The characteristics of REE and trace elements indicate that the oil shale formed in an oxygen-poor reducing environment and that the paleoclimatic conditions were relatively warm and humid. The degree of differentiation of REE indicates that the sedimentation rate in the study area was low, which reflected the characteristics of relatively deep sedimentary water bodies and distant source areas. The results also proved that the source rock mainly consisted of calcareous mudstone, and a small amount of granite was also mixed in.


2012 ◽  
Vol 43 (3) ◽  
pp. 262-274 ◽  
Author(s):  
J. Borrego ◽  
B. Carro ◽  
N. López-González ◽  
J. de la Rosa ◽  
J. A. Grande ◽  
...  

The concentration of rare earth elements together with Sc, Y, and U, as well as rare earth elements fractionation patterns, in the water of an affected acid mine drainage system were investigated. Significant dissolved concentrations of the studied elements were observed in the fluvial sector of this estuary system (Sc ∼ 31 μg L−1, Y ∼ 187 μg L−1, U ∼ 41 μg L−1, Σ rare earth elements ∼621 μg L−1), with pH values below 2.7. In the mixing zone of the estuary, concentrations are lower (Sc ∼ 2.1 μg L−1; Y ∼ 16.7 μg L−1; U ∼ 4.8 μg L−1; Σ rare earth elements ∼65.3 μg L−1) and show a strong longitudinal gradient. The largest rare earth elements removal occurs in the medium-chlorinity zone and it becomes extreme for heavy rare earth elements, as observed for Sc. Samples of the mixing zone show a North American Shale normalized pattern similar to the fluvial zone water, while the samples located in the zone with pH between 6.5 and 7.7 show a depletion of light rare earth elements relative to middle rare earth elements and heavy rare earth elements, similar to that observed in samples of the marine estuary.


2016 ◽  
Vol 25 (4) ◽  
pp. 60-67
Author(s):  
Sungeun Lee ◽  
Joung Woon Kim ◽  
Jong Hyuk Jeon ◽  
Hong Myeong Jun ◽  
Jin Young Lee ◽  
...  

2021 ◽  
Author(s):  
Bin Wang ◽  
Yuzhe Zhang ◽  
Wen Sun ◽  
Xudong Zheng ◽  
Zhongyu Li

The recovery of rare earth elements, especially heavy rare earth elements, from rare earth waste products has a high economic and environmental beneficial result. In this paper, cellulose nanocrystals used...


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