scholarly journals Trace elements geochemistry in high-incidence areas of liver-related diseases, northwestern Ethiopia

2019 ◽  
Vol 42 (5) ◽  
pp. 1235-1254
Author(s):  
Jemal Ahmed
Keyword(s):  
Trace Elements ◽  
Trace Element ◽  
Selenium Deficiency ◽  
Stream Sediments ◽  
Low Grade ◽  
Geochemical Background ◽  
Water Stream ◽  
Icp Ms ◽  
History Of ◽  
Trace Element Contents

Abstract This paper reports the results of trace elements geochemistry from Tigray national state, northwestern Ethiopia. The area is part of the Arabian-Nubian Shield, where the dominant exposure is low-grade metamorphic rocks and has a long history of liver-related diseases. The increase in the number of liver-related disease patients of the area has been an environmental health issue of national concern. The aim of the study is to determine the level of trace element concentrations and distributions in water and stream sediments of the area and identify the possible sources in relation to human health. Water, stream sediment and rocks samples (20 water, 20 stream sediments, and 6 rock samples) were collected in March 2011 and analyzed for major and trace element contents using ICP-MS, ICP-OES, ion Chromatography, and XRF methods. Bromine, aluminum, fluorine, arsenic, and nitrate values exceed the WHO maximum acceptable concentration (MAC) for drinking purpose. Bromine ranges from 0.11 to 1.48 mg/l show higher values in all samples, and fluorine ranges from 0.21 to 16.49 mg/l show higher values in 20% of the samples. Other trace elements are aluminum—30%, arsenic—10%, and nitrate (NO3)—10%, and they are examples of elements which have above MAC for drinking water. Selenium deficiency may be the other problematic element in the area for which its deficiency is associated with liver damage and heart muscle disorder. The concentration of cobalt and chromium exceeded world geochemical background value in average shale at most sample stations indicated that these stations were in potential risk.

Laser ablation ICP MS trace element composition of native gold from the Abitibi Greenstone belt, Timmins Ontario.

2021 ◽  
Author(s):  
John D. Greenough ◽  
Alejandro Velasquez ◽  
Mohamed Shaheen ◽  
Joel Gagnon ◽  
Brian J. Fryer ◽  
...  
Keyword(s):  
Trace Elements ◽  
Laser Ablation ◽  
Trace Element ◽  
Greenstone Belt ◽  
Native Gold ◽  
Internal Standard ◽  
Gold Deposits ◽  
Ore Deposits ◽  
Abitibi Greenstone Belt ◽  
Icp Ms

Trace elements in native gold provide a “fingerprint” that tends to be unique to individual gold deposits. Fingerprinting can distinguish gold sources and potentially yield insights into geochemical processes operating during gold deposit formation. Native gold grains come from three historical gold ore deposits; Hollinger, McIntyre (quartz-vein ore), and Aunor near Timmins, Ontario, at the western end of the Porcupine gold camp and the south-western part of the Abitibi greenstone belt. Laser-ablation, inductively-coupled plasma mass spectrometry (LA ICP MS) trace element concentrations were determined on 20 to 25 µm wide, 300 µm long rastor trails in ~ 60 native gold grains. Analyses used Ag as an internal standard with Ag and Au determined by a scanning electron microscope with an energy dispersive spectrometer. The London Bullion Market AuRM2 reference material served as the external standard for 21 trace element analytes (Al, As, Bi, Ca, Cr, Cu, Fe, Mg, Mn, Ni, Pb, Pd, Pt, Rh, Sb, Se, Si, Sn, Te, Ti, Zn; Se generally below detection in samples). Trace elements in native gold associate according to Goldschmidt’s classification of elements strongly suggesting that element behavior in native Au is not random. Such element behavior suggests that samples from each Timmins deposit formed under similar but slightly variable geochemical conditions. Chalcophile and siderophile elements provide the most compelling fingerprints of the three ore deposits and appear to be mostly in solid solution in Au. Lithophile elements are not very useful for distinguishing these deposits and element ABSTRACT CUT OFF BY SOFTWARE

Dating polymetamorphism using titanite: Linking trace elements, textures, and ages

2021 ◽  
Author(s):  
Jesse Walters ◽  
Alicia Cruz-Uribe ◽  
Won Joon Song ◽  
Joshua Stone ◽  
Hanna Brooks ◽  
...  
Keyword(s):  
Trace Elements ◽  
Trace Element ◽  
Bulk Composition ◽  
Granulite Facies ◽  
Compositional Variation ◽  
Excimer Laser Ablation ◽  
Eu Anomaly ◽  
Fluid Infiltration ◽  
Icp Ms ◽  
The University

<p>Here we present titanite U-Pb dates from two banded calc silicate gneisses (SSP18-1A and 1B) from western Maine. Mineral textures and compositions display multiple phases of metamorphism. The peak lower granulite facies assemblage is Di + Kfs + Pl + Ttn, with little to no calcite present. Late Czo + Tr replaces Di + Pl, suggesting an influx of X<sub>H2O</sub> > 0.90 fluids. Nearby metapelites show the transition from sillimanite-bearing to muscovite-bearing assemblages, indicating that fluid infiltration may be widespread. Compositional maps of clinopyroxene in SSP18-1B show fracturing and rehealing of early Fe-rich diopside with late Mg-rich diopside. Both samples exhibit overprinting of An-rich plagioclase by increasingly Ab-rich plagioclase. Titanite grains in both samples exhibit BSE textures and compositional variation consistent with multiple phases of growth and dissolution-reprecipitation reactions.</p><p>Titanite trace element and U-Pb data were collected by LA-ICP-MS at the University of Maine using an ESI NWR193<sup>UC</sup> excimer laser ablation system coupled to an Agilent 8900 ICP-MS. Single spot ages range from 280 to 400 Ma with 12-20 Ma propagated 2SE. Four composition-date domains are identified in SSP18-1B: A. 400 ± 8 Ma (dark BSE cores), B. 372 ± 4 Ma (bright BSE cores), C. 342 ± 6 Ma (bright BSE cores, no Eu anomaly), and D. 302 ± 3 Ma (dark BSE rims, low LREE). Titanite Fe and Y concentrations increase with decreasing date, whereas Sr concentrations decrease. In clinopyroxene, Fe and Y decrease between high Fe-diopside and late Mg-diopside, placing the fracturing and rehealing events between 400 and 372 Ma. Strontium concentrations in titanite decrease between subsequent generations of plagioclase, diopside, and titanite, suggesting a continual fractionation of Sr from the reactive bulk composition. Low LREE in ca. 300 Ma titanite domains in both samples are consistent with the formation of texturally late allanite and clinozoisite, thus constraining the timing of the high X<sub>H2O</sub> fluid infiltration event. Zr-in-titanite temperatures for rims in the quartz-bearing SSP18-1B give a weighted mean T of 764 °C at 4.5 GPa, consistent with the muscovite-absent sillimanite-bearing assemblage in garnet cores from metapelite samples. However, the 100-150 °C lower Grt-Bt temperatures for metapelites are not consistent with peak metamorphic phase equilibria. Our data demonstrate the utility of linking titanite textures and trace element concentrations with those of other minerals to reveal past metamorphic and deformational events. Additionally, we show that titanite may reliably preserve U and Pb isotopic ratios, trace elements, and textures over subsequent high-T metamorphic events.</p>

Deconvolution of the composition of fine-grained pyrite in sedimentary matrix by regression of time-resolved LA-ICP-MS data

2020 ◽  
Vol 105 (6) ◽  
pp. 820-832 ◽  
Author(s):  
Aleksandr S. Stepanov ◽  
Leonid V. Danyushevsky ◽  
Ross R. Large ◽  
Indrani Mukherjee ◽  
Irina A. Zhukova
Keyword(s):  
Trace Elements ◽  
Regression Analysis ◽  
Trace Element ◽  
Sedimentary Rocks ◽  
Trace Element Composition ◽  
Element Composition ◽  
Silicate Matrix ◽  
Time Resolved ◽  
Icp Ms ◽  
Wide Range

Abstract Pyrite is a common mineral in sedimentary rocks and is the major host for many chalcophile trace elements utilized as important tracers of the evolution of the ancient hydrosphere. Measurement of trace element composition of pyrite in sedimentary rocks is challenging due to fine-grain size and intergrowth with silicate matrix and other sulfide minerals. In this contribution, we describe a method for calculation of trace element composition of sedimentary pyrite from time-resolved LA-ICP-MS data. The method involves an analysis of both pyrite and pyrite-free sediment matrix, segmentation of LA-ICP-MS spectra, normalization to total, regression analysis of dependencies between the elements, and calculation of normalized composition of the mineral. Sulfur is chosen as an explanatory variable, relative to which all regressions are calculated. The S content value used for calculation of element concentrations from the regressions is calculated from the total, eliminating the need for independent constraints. The algorithm allows efficient measurement of concentrations of multiple chalcophile trace elements in pyrite in a wide range of samples, including quantification of detection limits and uncertainties while excluding operator bias. The data suggest that the main sources of uncertainties in pyrite composition are sample heterogeneity and counting statistics for elements of low abundance. The analysis of regression data of time-resolved LA-ICP-MS measurements could provide new insights into the geochemistry of the sedimentary rocks and minerals. It allows quantification of ratios of elements that do not have reference material available (such as Hg) and provides estimates on the content of non-sulfidic Fe in the silicate matrix. Regression analysis of the mixed LA-ICP-MS signal could be a powerful technique for deconvolution of phase compositions in complex multicomponent samples.

scholarly journals Serum Levels of Selenium, Zinc, Copper, Manganese, and Iron in Prostate Cancer Patients

2020 ◽  
Vol 14 (1) ◽  
pp. 44-49 ◽  
Author(s):  
Saleh A.K. Saleh ◽  
Heba M. Adly ◽  
Altaf A. Abdelkhaliq ◽  
Anmar M. Nassir
Keyword(s):  
Prostate Cancer ◽  
Trace Elements ◽  
Cancer Patients ◽  
Serum Levels ◽  
Cellular Growth ◽  
Control Groups ◽  
Icp Ms ◽  
Copper Manganese ◽  
Trace Element Contents ◽  
Serum Trace Elements

Backgrounds: Variations of trace element contents may be associated with several diseases including metabolic disorders, cellular growth disturbance, mutation and tumorigenesis. Prostate cancer is the second most common male cancer worldwide and stand fifth most common male cancer in Saudi Arabia. Objective: In the present study, Serum levels of selenium, zinc, copper, manganese, and iron were measured in patients with BPH and prostate cancer aiming to explore the association between these elements and prostate cancer. Patients and Methods: The study included 40 newly diagnosed prostate cancer patients, 22 patients with BPH and 30 healthy male subjects. All participant groups had similar socio-economic levels. Fasting blood samples were collected from all subjects and before any intervention for the patients. Serum PSA concentrations were analyzed by ELIZA and trace elements Se, Zn, Cu, Mn and Fe were measured by ICP-MS. Results: Serum Se, Zn, and Mn levels of prostate cancer patients were significantly decreased compared to control groups. The levels of serum Cu and Fe were significantly higher in prostate cancer patients than in control groups. Conclusion: In the present study, an association was noticed between serum trace elements disturbance and prostate cancer. The decreased levels of Se, Zn, and Mn, and increased Cu and Fe levels may play significant roles in the initiation of prostate cancer. However, future prospective studies on the causes of trace elements alteration in prostate cancer patients are needed as well as to illustrate the relation between different prostate cancer stages and trace elements concentrations.

Pyrite trace-element and sulfur isotope geochemistry of paleo-mesoproterozoic McArthur Basin: Proxy for oxidative weathering

2019 ◽  
Vol 104 (9) ◽  
pp. 1256-1272 ◽  
Author(s):  
Indrani Mukherjee ◽  
Ross R. Large ◽  
Stuart Bull ◽  
Daniel G. Gregory ◽  
Aleksandr S. Stepanov ◽  
...  
Keyword(s):  
Trace Elements ◽  
Trace Element ◽  
Sulfur Isotope ◽  
Gradual Increase ◽  
Isotope Geochemistry ◽  
Atmospheric Oxygen ◽  
Black Shales ◽  
Elemental Ratios ◽  
System A ◽  
Icp Ms

Abstract Redox-sensitive trace elements and sulfur isotope compositions obtained via in situ analyses of sedimentary pyrites from marine black shales are used to track atmosphere-ocean redox conditions between ∼1730 and ∼1360 Ma in the McArthur Basin, northern Australia. Three black shale formations within the basin (Wollogorang Formation 1730 ± 3 Ma, Barney Creek Formation 1640 ± 3 Ma, and Upper Velkerri Formation 1361 ± 21 Ma) display systematic stratigraphic variations in pyrite trace-element compositions obtained using LA-ICP-MS. The concentrations of several trace elements and their ratios, such as Se, Zn, Se/Co, Ni/Co, Zn/Co, Mo/Co, Se/Bi, Zn/Bi, Ni/Bi, increase from the stratigraphically lower Wollogorang Formation to the Upper Velkerri Formation. Cobalt, Bi, Mo, Cu, and Tl show a consistent decrease in abundance while Ni, As, and Pb show no obvious trends. We interpret these trace element trends as a response to the gradual increase of oxygen in the atmosphere-ocean system from ∼1730 to 1360 Ma. Elements more mobile during erosion under rising atmospheric oxygen show an increase up stratigraphy (e.g., Zn, Se), whereas elements that are less mobile show a decrease (e.g., Co, Bi). We also propose the increase of elemental ratios (Se/Co, Ni/Co, Zn/Co, Mo/Co, Ni/Bi, and Zn/Bi) up stratigraphy are strong indicators of atmospheric oxygenation. Sulfur isotopic compositions of marine pyrite (δ34Spyrite) from these formations, obtained using SHRIMP-SI, are highly variable, with the Wollogorang Formation exhibiting less variation (δ34S = –29.4 to +9.5‰; mean –5.03‰) in comparison to the Barney Creek (δ34S = –13.8 to +41.8‰; mean +19.88‰) and Velkerri Formations (δ34S = –14.2 to +52.8‰; mean +26.9‰). We propose that the shift in mean δ34S to heavier values up-section corresponds to increasing deep water oxygenation from ∼1730 to 1360 Ma. Incursion of oxygenated waters possibly caused a decrease in the areal extent of anoxic areas, at the same time, creating a possibly efficient reducing system. A stronger reducing system caused the δ34S of the sedimentary pyrites to become progressively heavier. Interestingly, heavy δ34S in pyrites overlaps with the increase in the concentration of certain trace elements (and their ratios) in sedimentary pyrites (Se, Zn, Se/Co, Ni/Co, Zn/Co, Mo/Co, Ni/Bi, and Zn/Bi). This study concludes that there was a gradual increase of atmospheric oxygen accompanied by ocean oxygenation through the first ∼400 million years of the Boring Billion (1800–1400 Ma) in the McArthur Basin.

scholarly journals Trace Elements in Magnetite from the Pagoni Rachi Porphyry Prospect, NE Greece: Implications for Ore Genesis and Exploration

Minerals ◽  
2019 ◽  
Vol 9 (12) ◽  
pp. 725 ◽  
Author(s):  
Constantinos Mavrogonatos ◽  
Panagiotis Voudouris ◽  
Jasper Berndt ◽  
Stephan Klemme ◽  
Federica Zaccarini ◽  
...  
Keyword(s):  
Trace Elements ◽  
Laser Ablation ◽  
Trace Element ◽  
Inductively Coupled Plasma ◽  
Ore Deposits ◽  
Hydrothermal Conditions ◽  
Northern Greece ◽  
Icp Ms ◽  
Accessory Phase ◽  
Granodiorite Porphyry

Magnetite is a common accessory phase in various types of ore deposits. Its trace element content has proven to have critical implications regarding petrogenesis and as guides in the exploration for ore deposits in general. In this study we use LA-ICP-MS (laser ablation-inductively coupled plasma-mass spectrometry) analyses of trace elements to chemically characterize magnetite from the Pagoni Rachi Cu–Mo–Re–Au porphyry-style prospect, Thrace, northern Greece. Igneous magnetite mostly occurs as euhedral grains, which are commonly replaced by hematite in fresh to propylitic-altered granodiorite porphyry, whereas, hydrothermal magnetite forms narrow veinlets or is disseminated in sodic/potassic-calcic altered (albite + K-feldspar + actinolite + biotite + chlorite) granodiorite porphyry. Magnetite is commonly associated with chalcopyrite and pyrite and locally exhibits martitization. Laser ablation ICP-MS analyses of hydrothermal magnetite yielded elevated concentrations in several trace elements (e.g., V, Pb, W, Mo, Ta, Zn, Cu, and Nb) whereas Ti, Cr, Ni, and Sn display higher concentration in its magmatic counterpart. A noteworthy enrichment in Mo, Pb, and Zn is an unusual feature of hydrothermal magnetite from Pagoni Rachi. High Si, Al, and Ca values in a few analyses of hydrothermal magnetite imply the presence of submicroscopic or nano-inclusions (e.g., chlorite, and titanite). The trace element patterns of the hydrothermal magnetite and especially the decrease in its Ti content reflect an evolution from the magmatic towards the hydrothermal conditions under decreasing temperatures, which is consistent with findings from analogous porphyry-style deposits elsewhere.

scholarly journals Effect of cobalt supplementation on lamb growth rates in the face of cobalt deficiency

2020 ◽  
Vol 8 (2) ◽  
pp. e001099
Author(s):  
Kim Hamer ◽  
Hannah Mylin ◽  
Donald Barrie ◽  
Valentina Busin ◽  
Katharine Denholm
Keyword(s):  
Trace Elements ◽  
Trace Element ◽  
Blood Sample ◽  
Growth Rates ◽  
Selenium Deficiency ◽  
Blood Samples ◽  
The Face ◽  
Cobalt Deficiency ◽  
Lamb Growth

A hill farm in eastern Scotland had noted poor lamb growth rates since 2014. Cobalt, selenium and copper deficiencies were reported from historical blood sample results, and trace element supplementation had been administered to the ewes, but not the lambs. A supplementation trial was undertaken in 2018 to compare the daily liveweight gain (DLWG) between lambs supplemented with trace elements and unsupplemented lambs. The trace element supplements used were intraruminal boluses containing 51-mg cobalt, 10-mg selenium and 60-mg iodine (Downland Essential Lamb bolus, Downland). Blood samples taken two months postsupplementation showed that unsupplemented lambs had cobalt-deficient status, but not selenium deficiency. Lambs supplemented with the trace element boluses had an increase in DLWG of 49 g/day compared with unsupplemented lambs. This case confirms that cobalt supplementation on deficient farms can be associated with a significant improvement in growth rates of growing lambs on Scottish hill farms.

Insights into chemical mobility in titanite driven by low-temperature crystal-plastic deformation

2021 ◽  
Author(s):  
Nicholas Udy ◽  
Michael Stearns
Keyword(s):  
Plastic Deformation ◽  
High Temperature ◽  
Low Temperature ◽  
Crystal Lattice ◽  
Trace Element ◽  
Fault Zone ◽  
Temperature Deformation ◽  
Icp Ms ◽  
Trace Element Contents ◽  
Element Contents

<p>The U-Pb system in titanite has been shown to be reset during a variety of high-temperature processes including high-temperature deformation, but post-deformation modification and recovery of crystal-lattice strain have so far made U-Pb equilibration mechanism from deformed titanites equivocal. Microstructures, including mechanical twinning and subgrain rotation recrystallization are more likely to be preserved at low-temperatures, but the systematics of chemical equilibration have not been established for these conditions. This study identifies progressive crystallographic misorientation and deformation twins in titanite porphyroclasts from the Wasatch Fault Zone, Utah, USA. The microstructures, mapped using electron backscatter diffraction (EBSD), developed at ~11 km depth during 300–400 ºC crystal-plastic deformation within the ductile fault zone. These microstructural maps were used to guide laser ablation-split stream ICP-MS analysis: U-Pb isotopes measured in tandem with major and trace element contents. Despite the low temperature, U-Pb and trace element contents in titanite equilibrated, at least partially, during deformation. Both major and trace elements in titanite also likely partitioned with a fluid and in response to the (re)crystallization of other mineral phases in the fault zone. Chemical zoning and crystal lattice recovery suggestive of fluid-aided recrystallization are absent, and the main mechanism for this resetting may instead be an enhancement of element mobility along microstructure dislocations. These processes are interpreted to record complex open-system behavior of titanite caused by crystal-plastic deformation during the initiation of the WFZ. This presentation will summarize the comparative analysis of microstructure by EBSD and titanite chemistry by LASS-ICP-MS, and how it bears on the understanding of elemental mobility in titanite during low-temperature crystal-plastic deformation.</p>

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