Pyrite Oxidation Controlled Siderophile Element Accumulation on the K-Pg Boundary at El Kef, Tunisia

Author(s):  
Munir Humayun ◽  
Steffanie Sillitoe-Kukas ◽  
Thierry Adatte ◽  
Gerta Keller

<p>In a transformative contribution, Alvarez et al. (1980) discovered the iridium anomaly at several K-Pg boundary locations that they attributed to an extraterrestrial impact that triggered the end-Cretaceous extinction. The absence of a suitable mechanism by which to concentrate siderophile elements in the boundary clay drove the argument for an extraterrestrial origin of the iridium. They made the observation that fallout from a fireball would be expected to create a uniform distribution of Ir in the clay layer and puzzled over the scale of lateral variation in Ir observed even then. A detailed global study of the siderophile element (Ru, Rh, Pd, Ir, Pt Au) distribution at the K-Pg boundary found non-chondritic patterns concluding that some post-depositional process(es) must have affected the elemental distribution (Goderis et al., 2015). Such processes would mobilize siderophile elements into the surrounding strata. Here, we applied laser ablation ICP-MS, a microanalytical technique, to investigate the distribution of 60 elements, with an emphasis on the siderophile elements, in a vertical transect at the K-Pg boundary at El Kef, Tunisia, to search for elemental transport in or out of the K-Pg clay layer. The K-Pg boundary at El Kef consists of irregular mixed layers of clay, goethite and gypsum with marls above and below. The siderophile elements are concentrated in the goethite-rich component with a distinctly terrestrial crust pattern, albeit super-enriched, with prominent negative Pt anomalies indicative of deposition from an oxidized solution. The Fe/Se ratio indicates an origin of the goethite by oxidation of sedimentary pyrite. Iron oxyhydroxides are effective substrates for the binding of trace metal oxyanions from solution. The extreme enrichment of siderophile elements reflects long-term concentration of siderophile elements from percolating oxidized groundwaters at El Kef. The sulfuric acid produced by pyrite oxidation was neutralized by calcium carbonate in the marls to form gypsum. Selenium (normally a sulfur analog) is undetectable in the El Kef gypsum endmember (Se/S~0), unlike marine gypsum, supporting a formation by pyrite oxidation. This observation potentially explains the ubiquitous non-chondritic siderophile patterns observed globally and the variable Ir enrichments that puzzled geochemists since Alvarez et al. (1980). In view of this observation, siderophile element enrichment in the K-Pg layer can no longer be taken as unambiguous evidence of an extraterrestrial impact.</p>

2010 ◽  
Vol 7 (8) ◽  
pp. 2339-2350 ◽  
Author(s):  
D. Munsel ◽  
U. Kramar ◽  
D. Dissard ◽  
G. Nehrke ◽  
Z. Berner ◽  
...  

Abstract. The incorporation of heavy metals into carbonate tests of the shallow water benthic foraminifer Ammonia tepida was investigated under controlled laboratory conditions. Temperature, salinity, and pH of the culture solutions were kept constant throughout the duration of this experiment, while trace metal concentrations were varied. Concentrations of Ni, Cu, and Mn were set 5-, 10-, and 20 times higher than levels found in natural North Sea water; for reference, a control experiment with pure filtered natural North Sea water was also analysed. The concentrations of Cu and Ni from newly grown chambers were determined by means of both μ-synchrotron XRF and Laser Ablation Inductively Coupled Plasma Mass Spectroscopy (LA-ICP-MS). The results of both independent analytical techniques agreed within the analytical uncertainty. In general, the concentration of the analysed elements in the tests increased in line with their concentration in the culture solutions. Potential toxic and/or chemical competition effects might have resulted in the decreased incorporation of Ni and Cu into the calcite of the specimens exposed to the highest elemental concentrations. Mn incorporation exhibited large variability in the experiment with the 20-fold increased element concentrations, potentially due to antagonistic effects with Cu. The partition coefficients of Cu and Ni were calculated to be 0.14 ± 0.02 and 1.0 ± 0.5, respectively, whereas the partition coefficient of Mn was estimated to be least 2.4. These partition coefficients now open the way for reconstructing past concentrations for these elements in sea water.


2018 ◽  
Vol 33 (2) ◽  
pp. 187-194 ◽  
Author(s):  
Georgina M. Thyssen ◽  
Claudia Keil ◽  
Melanie Wolff ◽  
Michael Sperling ◽  
Daniel Kadow ◽  
...  

The distribution of several nutritional and toxic elements in cocoa beans is visualized for the first time using LA-ICP-MS.


2001 ◽  
Vol 11 (03n04) ◽  
pp. 125-131 ◽  
Author(s):  
Y. WATANABE ◽  
S. HOMMA-TAKEDA ◽  
M. YUKAWA ◽  
Y. NISHIMURA ◽  
H. IMASEKI

Micro-PIXE and inductively coupled plasma mass spectrometry (ICP-MS) were applied to elemental distribution analyses in plant root apex which is composed of various types of tissues and cells in different developmental stages. ICP-MS was so sensitive that a large number of elements including Na, Mg, P, S, K, Ca, Mn, Fe, Cu, Zn, Se, Rb, Sr and Cs could be determined quantitatively. These fourteen elements included almost all the essential elements for plant growth. Only a rough estimation, however, could be obtained by ICP-MS for the elemental distribution at the tissue level, by analyzing sections from the root apex. On the other hand, micro-PIXE was effective for detailed mappings of elemental distributions. The images of elemental distributions were obtained for Na, Mg, P, S, K, Ca, Mn, Fe and Zn, corresponding to the microscopic images of the root structures. The localizations of P, K and Zn in some tissues were observed by the mappings. These results indicated that micro-PIXE and ICP-MS have different, but complementary abilities for the investigation of elemental distributions in plant tissues.


2015 ◽  
Vol 30 (8) ◽  
pp. 1809-1815 ◽  
Author(s):  
Maximilian Bonta ◽  
Andreas Limbeck ◽  
C. Derrick Quarles Jr ◽  
Dayana Oropeza ◽  
Richard E. Russo ◽  
...  

The quality of LA-ICP-MS images can be determined using a metric describing the accordance of measured and actual elemental distribution.


2017 ◽  
Vol 44 ◽  
pp. 26-31 ◽  
Author(s):  
Oliver Hachmöller ◽  
Andree Zibert ◽  
Hans Zischka ◽  
Michael Sperling ◽  
Sara Reinartz Groba ◽  
...  

Minerals ◽  
2020 ◽  
Vol 10 (9) ◽  
pp. 798
Author(s):  
Alvar Soesoo ◽  
Johannes Vind ◽  
Sigrid Hade

We provide a compilation of geology of uranium and thorium potential resources in the Ordovician black shale (graptolite argillite), Cambrian–Ordovician shelly phosphorite and in the secondary resources (tailings) of Estonia. Historical and new geological, XRF and ICP-MS geochemical data and ArcGIS modeling results of elemental distribution and tonnages are presented. The Estonian black shale contains 5.666 million tons of U, 16.533 Mt Zn, 12.762 Mt Mo, 47.754 Mt V and 0.213–0.254 Mt of Th. The Estonian phosphate resources, altogether about 3 billion metric tons of phosphate ore, contain about 147,000 to 175,000 tons of U. Rare earth element concentrations in the phosphorite ore average at 1200–1500 ppm of ΣREE. Thorium can also be a possible co-product. The mining waste dump at the Maardu contains at least 3650 tons of U and 730 tons of Th. The Sillamäe radioactive waste depository contains about 1200 tons of U and 800 tons of Th. Due to the neighboring geological positions, as well as environmental constraints and mining technologies, the black shale and phosphorite can be treated as a complex multi-resource, possibly at the continental scale, which needs to be extracted together.


2018 ◽  
Vol 2018 ◽  
pp. 1-9 ◽  
Author(s):  
Yun Jung Jang ◽  
Jihye Lee ◽  
Kang-Bong Lee ◽  
Donghwan Kim ◽  
Yeonhee Lee

Recently, Cu(InXGa(1−X))Se2 (CIGS) absorber layers have been extensively studied by many research groups for thin-film solar cell technology. CIGS material is particularly promising due to its exceptionally high absorption coefficient and large band gap range, which is adjustable as a function of alloy stoichiometry. To enhance the conversion performance of CIGS solar cells, understanding the CIGS structure and composition is a crucial challenge. We conducted a quantitative study to determine the bulk composition of the major elements such as Cu, In, Ga, and Se of four different CIGS photovoltaic cells. The compositional information was obtained by X-ray fluorescence (XRF), inductively coupled plasma atomic emission spectroscopy (ICP-AES), and femtosecond laser ablation inductively coupled plasma mass spectrometry (fs-LA-ICP-MS). Then, the XRF concentration ratio was compared with the intensity ratio of fs-LA-ICP-MS to investigate the potential of accurate and rapid analysis using the fs-LA-ICP-MS technique. In contrast to the bulk information, the surface techniques can supply detailed information about the chemical composition across the depth profile. Here, elemental depth distributions of CIGS thin films were investigated using magnetic sector secondary ion mass spectrometry (SIMS) and Auger electron spectroscopy (AES). The atomic distributions of four different CIGS absorber layers exhibited a good agreement although they were obtained using two different surface instruments, AES and SIMS. Comparative analysis results of different CIGS absorber layers using SIMS, AES, and fs-LA-ICP-MS provide us with the appropriate technique for the information of accurate composition in a rapid analysis time. Thanks to a simple approach using the Ga/(In + Ga) ratio, the optical band gap energy of the Cu(InXGa(1−X))Se2 quaternary layer was monitored in the entire CIGS layer. The elemental distribution and the band gap determination were then used to elucidate their relationship to the corresponding CIGS cell efficiency result.


RSC Advances ◽  
2017 ◽  
Vol 7 (33) ◽  
pp. 20510-20519 ◽  
Author(s):  
G. Bauer ◽  
B. Achleitner ◽  
M. Bonta ◽  
G. Friedbacher ◽  
A. Limbeck

Analysis of single particles (∼100 μm) with LA-ICP-MS achieving lateral resolved composition of trace elementsvia2D-imaging.


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