Rare earth element mobilization from marine atmospheric dust into seawater

1994 ◽  
Vol 46 (3) ◽  
pp. 255-260 ◽  
Author(s):  
M.J. Greaves ◽  
P.J. Statham ◽  
H. Elderfield
2018 ◽  
Vol 2 (5) ◽  
pp. 506-520 ◽  
Author(s):  
Michael C. Cheshire ◽  
David L. Bish ◽  
John F. Cahill ◽  
Vilmos Kertesz ◽  
Andrew G. Stack

2021 ◽  
Vol 11 (30) ◽  
Author(s):  
Tesleem O. Kolawole ◽  
Omowunmi S. Olatunji ◽  
Olumuyiwa M. Ajibade ◽  
Charles A. Oyelami

Background. Rare earth element (REE) composition of atmospheric dust has recently been used to trace potential sources of dust pollution. Objective. The present study aimed to determine the sources of atmospheric pollution in the study area using REE patterns and determine their level of pollution. Methods. Twenty-five (25) atmospheric dust samples were collected in the study area, with five samples each from an industrial area, traffic area, dumpsite area, residential area and remote area in Ibadan, southwestern Nigeria. In addition, five (5) topsoil and two (2) rock samples (granite gneiss) were collected for comparison. Concentrations of REE were determined by inductively coupled plasma mass spectrometry (ICP-MS). Results. The ratio of lanthanum/cerium (La/Ce), especially in some locations in industrial area (1.5), traffic area (1.5) and to some extent dumpsite area (1.1) was higher than in soil (0.2), upper continental crust (0.5) and the minimum value of fluid catalytic crackers (1.0). Generally, the respective average values of the ratios of La/praseodymium (Pr), La/neodymium (Nd) and La/samarium (Sm) in industrial area (32.1, 7.8 and 52.6) and traffic area (14.9, 4.4 and 26.8) were higher than their respective averages in soil (4.4, 1.1 and 6.2), rock (5.7, 1.9 and 14.1), upper continental crust (4.4, 1.1 and 6.6) and the minimum value in fluid catalytic crackers (5.8, 3.7 and 37.0). Meanwhile, their corresponding value in the dumpsite area, residential area and remote area were lower or similar to the geological background levels. Discussion. The contamination factors of REEs in the atmospheric dust of the industrial area and traffic area were classified as heavily contaminated, especially with light lanthanoid elements in REE. The degree of contamination of REEs in the atmospheric dust of industrial area (30.9) and traffic area (18.8) fell within the considerable contamination category. The high values of the light lanthanoid ratio and the contamination indices were attributed to their emission from the fired-power plant and vehicular exhaust. Conclusions. Most of the composition of the atmospheric dust was sourced from the local geology of the study area as observed in the residential area and remote area, while the contamination in the industrial area and traffic area was attributed to human activities. Competing Interests. The authors declare no competing financial interests.


Geosphere ◽  
2019 ◽  
Vol 15 (6) ◽  
pp. 1958-1972
Author(s):  
Gavin Piccione ◽  
E. Troy Rasbury ◽  
Brent A. Elliott ◽  
J. Richard Kyle ◽  
Steven J. Jaret ◽  
...  

Abstract Numerous studies have documented rare-earth element (REE) mobility in hydrothermal and metamorphic fluids, but the processes and timing of REE mobility are rarely well constrained. The Round Top laccolith in the Trans-Pecos magmatic province of west Texas, a REE ore prospect, has crosscutting fractures filled with fluorite and calcite along with a variety of unusual minerals. Most notably among these is an yttrium and heavy rare-earth element (YHREE) carbonate mineral, which is hypothesized to be lokkaite based on elemental analyses. While the Round Top laccolith is dated to 36.2 ± 0.6 Ma based on K/Ar in biotite, U-Pb fluorite and nacrite ages presented here clearly show the mineralization in these veins is younger than 6.2 ± 0.4 Ma (the age of the oldest fluorite). This discrepancy in dates suggests that fluids interacted with the laccolith to mobilize REE more than 30 m.y. after igneous emplacement. The timing of observed REE mobilization overlaps with Rio Grande rift extension, and we suggest that F-bearing fluids associated with extension may be responsible for initial mobilization. A later generation of fluids was able to dissolve fluorite, and we hypothesize this later history involved sulfuric acid. Synchrotron spectroscopy and laser ablation–inductively coupled plasma–mass spectrometry (LA-ICP-MS) U-Pb dating of minerals that record these fluids offer tremendous potential for a more fundamental understanding of processes that are important not only for REE but other ore deposits as well.


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