scholarly journals Rare Earth Elements Variations in a Hyperacid Crater Lake and Their Relations With Changes in Phreatic Activity, Physico-Chemical Parameters, and Chemical Composition: The Case of Poás Volcano (Costa Rica)

2022 ◽  
Vol 9 ◽  
Author(s):  
Sabrina Pappaterra ◽  
Claudio Inguaggiato ◽  
Dmitri Rouwet ◽  
Raúl Mora-Amador ◽  
Carlos Ramírez-Umaña ◽  
...  

Decades of geochemical monitoring at active crater lakes worldwide have confirmed that variations in major elements and physico-chemical parameters are useful to detect changes in volcanic activity. However, it is still arduous to identify precursors of single phreatic eruptions. During the unrest phase of 2009–2016, at least 679 phreatic eruptions occurred at the hyperacid and hypersaline crater lake Laguna Caliente of Poás volcano (Costa Rica). In this study, we investigate the temporal variations of Rare Earth Elements (REE) dissolved in Laguna Caliente in order to 1) scrutinize if they can be used as a new geochemical tool to monitor changes of phreatic activity at hyperacid crater lakes and 2) identify the geochemical processes responsible for the variations of REE concentrations in the lake. The total concentration of REE varies from 950 to 2,773 μg kg−1. (La/Pr)N-local rock ratios range from 0.93 to 1.35, and Light REE over Heavy REE (LREE/HREE)N-local rock ratios vary from 0.71 to 0.95. These same parameters vary in relation to significant changes in phreatic activity; in particular, the (La/Pr)N-local rock ratio increases as phreatic activity increases, while that of (LREE/HREE)N-local rock decreases when phreatic activity increases. REE concentrations and their ratios were compared with the variations of major elements and physico-chemical parameters of the lake. Calcium versus (La/Pr)N-local rock and versus (LREE/HREE)N-local rock ratios show different trends compared to the other major elements (Na, K, Mg, Al, Fe, SO4, and Cl). Moreover, a higher loss of Ca (up to 2,835 ppm) in lake water was found with respect to the loss of Al, K, and Na. This loss of Ca is argued to be due to gypsum precipitation, a process corroborated by the mass balance calculation simulating the precipitation of gypsum and the contemporaneous removal of REE from the lake water. The observed relations between REE, changes in phreatic activity, and the parameters commonly used for the monitoring of hyperacid volcanic lakes encourage investigating more on the temporal and cause-effect relationship between REE dynamics and changes in phreatic activity at crater lake-bearing volcanoes.

2020 ◽  
Vol 34 (2) ◽  
pp. 183-194
Author(s):  
Alexandre Chaves ◽  
Luiz Knauer

The hematitic phyllite is a rock that occurs in the São João da Chapada and Sopa-Brumadinho formations of the southern Espinhaço range. Its origin is widely discussed in papers on Espinhaço, but there is no consensus on its protolith due to certain characteristics of the lithotype, such as its chemical composition and textural features. The pattern of rare earth elements strongly enriched [(La/Yb)N 6.80-17.68], with light rare earth elements [(La/Sm)N 2.54-4.83] richer than heavy ones [(Gd/Yb)N 1.28-3,32], suggests that the protolith was an alkaline volcanic rock formed during the rift that generated the Espinhaço basin. The major elements indicate that the alkaline rock met weathering processes, becoming a regolith. During the Brasiliano metamorphism, it finally became hematitic phyllite. Other characteristics of the lithotype, such as the presence of sericite-bearing rounded parts (possibly formed by alteration and deformation of leucite crystals) and the preservation of igneous layering, suggest a potassic volcanic origin for hematitic phyllite. In diagram that allows identifying altered and metamorphic volcanic rocks, the investigated samples have composition similar to a feldspathoid-rich alkali-basalt, probably a leucite tephrite, a leucitite or even a lamproite, rocks from mantle source.


1992 ◽  
Vol 54 (6) ◽  
pp. 494-503 ◽  
Author(s):  
Gary L Rowe ◽  
Shinji Ohsawa ◽  
Bokuichiro Takano ◽  
Susan L Brantley ◽  
Jose F Fernandez ◽  
...  

1992 ◽  
Vol 49 (1-2) ◽  
pp. 23-51 ◽  
Author(s):  
Gary L. Rowe ◽  
Susan L. Brantley ◽  
Mario Fernandez ◽  
Jose F. Fernandez ◽  
Andrea Borgia ◽  
...  

2019 ◽  
Vol 486 (5) ◽  
pp. 583-587
Author(s):  
A. M. Agashev

The paper presents the results of major and trace elements composition study of garnet megacrysts from Mir kimberlite pipe. On the major elements composition those garnets classified as low Cr and high Ti pyropes. Concentrations of TiO2 show a negative correlation with MgO и Cr2O3 contents in megacrysts composition. Fractional crystallization modeling indicates that the most appropriate melt to reproduce the garnet trace elements signatures is the melt of picritic composition. Composition of garnets crystallized from kimberlite melt do not correspond to observed natural garnets composition. Kimberlites contain less of Ti, Zr, Y and heavy REE (rare earth elements) but more of very incompatible elements such as light REE, Th, U, Nb, Ba then the model melt composition that necessary for garnet crystallization.


2016 ◽  
Author(s):  
Dabhade D. S. and Tandale M. R Dabhade D. S. and Tandale M. R ◽  

2001 ◽  
Vol 34 (3) ◽  
pp. 1255
Author(s):  
S. PANILAS ◽  
G. HATZIYANNIS

Multivariate statistical analysis was used on existing geochemical data of the Drama lignite deposit, eastern Macedonia, Greece. Factor analysis with varimax rotation technique was applied to study the distribution of major, trace and rare earth elements in the lignite and 850°C lignitic ash, to find a small set of factors that could explain most of the geochemical variability. The study showed that major elements AI, Na, Κ, contained in the lignite samples, presented high correlation with most of the trace and rare earth elements. In 850°C lignitic ashes major and trace elements present different redistribution. Only Al remained correlated with the trace elements Co, Cr, Rb, Ta, Th, Ti, Sc and rare earths related with inorganic matter in the lignite beds. Trace elements Fe, Mo, U, V, W, and Lu were associated with organic matter of lignite and had also been affected by the depositional environment.


1991 ◽  
Vol 28 (9) ◽  
pp. 1429-1443 ◽  
Author(s):  
Luc Harnois ◽  
John M. Moore

Samples of two subalkaline metavolcanic suites, the Tudor formation (ca. 1.28 Ga) and the overlying Kashwakamak formation, have been analysed for major elements and 27 trace elements (including rare-earth elements). The Tudor formation is tholeiitic and contains mainly basaltic flows, whereas the Kashwakamak formation is calc-alkaline and contains mainly andesitic rocks with minor felsic rocks. The succession has been regionally metamorphosed to upper greenschist – lower amphibolite facies. Trace-element abundances and ratios indicate that rocks of the Tudor and Kashwakamak formations are island-arc type. Geochemical modelling using rare-earth elements, Zr, Ti, and Y indicates that the Tudor volcanic rocks are not derived from a single parental magma through simple fractional crystallization. Equilibrium partial melting of a heterogeneous Proterozoic upper mantle can explain the trace-element abundances and ratios of Tudor formation volcanic rocks. The intermediate to felsic rocks of the Kashwakamak formation appear to have been derived from a separate partial melting event. The data are consistent with an origin of the arc either on oceanic crust or on thinned continental crust, and with accretion of the arc to a continental margin between the time of extrusion of Tudor volcanic rocks and that of Kashwakamak volcanic rocks.


2006 ◽  
Vol 985 ◽  
Author(s):  
Timothy E Payne ◽  
Reto Giere ◽  
Kaye P Hart ◽  
Gregory R Lumpkin ◽  
Peter J McGlinn

AbstractChemical extraction techniques and scanning electron microscopy were used to study the distribution and behavior of actinides and rare earth elements (REE) in hydrothermal veins at Adamello, (Italy). The six samples discussed in this paper were from the phlogopite zone, which is one of the major vein zones. The samples were similar in their bulk chemical composition, mineralogy, and leaching behavior of major elements (determined by extraction with 9M HCl). However, there were major differences in the extractability of REE and actinides. The most significant influence on the leaching characteristics appears to be the amounts of U, Th and REE incorporated in resistant host phases. Uranium and Th are very highly enriched in zirconolite grains. Actinides were more readily leached from samples with a higher content of U and Th, relative to the amount of zirconolite. The results show that REE and actinides present in chemically resistant minerals can be retained under aggressive leaching conditions.


Sign in / Sign up

Export Citation Format

Share Document