scholarly journals Geochemical Fractions of Heavy Metals in Bottom Sediments of the Pobeda Hydrothermal Cluster in the Mid-Atlantic Ridge (17°07′–17°08′ N)

Minerals ◽  
2021 ◽  
Vol 11 (6) ◽  
pp. 591
Author(s):  
Liudmila Demina ◽  
Irina Gablina ◽  
Dmitry Budko ◽  
Olga Dara ◽  
Aleksandra Solomatina ◽  
...  

In this study, to better understand the influence of hydrothermal processes on ore metal accumulation in bottom sediments, we examined distribution of Fe, Mn, Cu, Zn, As, and Pb in core of metalliferous sediments from the Pobeda hydrothermal cluster, and in core of non-mineralized (background) carbonate sediments (located 69 km northwards). Mechanisms of Fe, Mn, Cu, and Zn accumulation in sediments (12 samples) were evaluated based on sequential extraction of geochemical fractions, including a conditional mobile (F-1, exchangeable complex; F-2, authigenic Fe-Mn oxyhydroxides and associated metals; F-3, metals bound to organic matter/sulfides), and residual (F-4), fixed in crystalline lattices ones. The element contents were determined by the XRF and AAS methods, total carbon (TC) and total organic carbon (TOC) were determined using a Shimadzu TOC-L-CPN. Mineral composition and maps of element distribution in sediment components were obtained using the XRD and SEM-micro-X-ray spectrometry methods, respectively. In metalliferous sediments, according to our data, the major Fe mineral phase was goethite FeOOH (37–44% on a carbonate-free basis, cfb). In the metalliferous core, average contents (cfb), of Fe and Mn were 32.1% and 0.29%, whereas those of Cu, Zn, Pb, and As, were 0.74%, 0.27%, 0.03%, and 0.02%, respectively. Metalliferous sediments are enriched in Fe, Cu, Zn, Pb, and As, relatively to background ones. The exception was Mn, for which no increased accumulation in metalliferous core was recorded. Essential mass of Fe (up to 70% of total content) was represented by the residual fraction composed of crystallized goethite, aluminosilicates, the minerals derived from bedrock destruction processes mineral debris. Among geochemically mobile fractions, to 80% Fe of the (F-1 + F-2 + F-3) sum was determined in the form of F-2, authigenic oxyhydroxides. The same fraction was a predominant host for Mn in both metalliferous and background sediments (to 85%). With these Fe and Mn fractions, a major portion of Cu, Zn, and Pb was associated, while a less their amount was found in sulfide/organic fraction. In the metalliferous sediment core, maximal concentrations of metals and their geochemically mobile fractions were recorded in the deeper core sediment layers, an observation that might be attributed to influence of hydrothermal diffused fluids. Our data suggested that ore metals are mostly accumulated in sediment cores in their contact zone with the underlying serpentinized peridotites.

2021 ◽  
Vol 6 (1) ◽  
pp. 14
Author(s):  
Liudmila Demina ◽  
Irina Gablina ◽  
Olga Dara ◽  
Dmitry Budko ◽  
Nina Gorkova ◽  
...  

We examined the distribution of Fe, Mn, Cu, Zn, and Pb in one core of metalliferous, and one core of non-mineralized (background) carbonate sediments (located 69 km northwards), from the Pobeda hydrothermal field. Mechanisms of metal accumulation in sediments (12 samples) were evaluated based on sequential extraction of geochemical fractions, including mobile (exchangeable complex, authigenic Fe-Mn hydroxides, and sulfides), and lithogenic (fixed in crystalline lattices) forms. Maps of element distribution in sediment components were obtained using a scanning electron microscope equipped with an energy-dispersive spectrometry detector. In metalliferous sediments, according to X-ray diffraction data, the main Fe mineral phase was goethite FeOOH (37–44% on a carbonate-free basis). The contents of Fe and Mn reached 31.6 and 0.18%, respectively, whereas concentrations of Cu, Zn and Pb were 0.98, 0.36, and 0.059%. The coefficient of metal enrichment relative to background values varied from 16 to 125 times. The exception was Mn, for which no increased accumulation was recorded. Essential mass of Fe (up to 70% of total content) was represented by the residual fraction composed of crystallized goethite, aluminosilicates, the minerals derived from bedrock destruction processes. Among geochemically mobile fractions, 90–97% of total Fe was found in the form of authigenic oxyhydroxides. The same fraction was the predominant host for Mn in both metalliferous and background sediments (55–85%). A total of 40–96 % of Cd, Cu, Zn, and Pb were associated with these Fe and Mn fractions. The sulfide fraction amounted to roughly 10% of each metal. In metalliferous sediment core, the maximum concentrations of metals and their geochemically mobile fractions were recorded in deeper core intercepts, an observation that might be attributed to influence of hydrothermal diffused fluids. Our data suggested that metals are mostly accumulated in carbonate sediments in their contact zone with the underlying serpentinized basalts.


2021 ◽  
pp. 431-444
Author(s):  
L.L. Demina ◽  
◽  
D.F. Budko ◽  
N.V. Politova ◽  
T.N. Alexeeva ◽  
...  

Research results of geochemical fractions and distribution pattern of the major and trace elements in the sediment cores of the Barents Sea are presented. In the sediment core AMK- 5193, located in the central part of the sea, Al, Cr and Ni were detected predominantly in the lithogenic form (75−97% of the total content) throughout the core. A large or a noticeable portion (from 65% to 30% from total contents) of Pb, Cd, Cu, Ni, Co, Mn, and As was found to be accumulated due to hydrogenous processes, such as adsorption on amorphous Fe-Mn oxyhydroxides and clay particles. In the uppermost oxidized layer (0−6 cm) of St. AMK-5193, where the most intensive exchange processes between the solid and liquid phases of bottom sediments happen, a significant increase in the proportion of geochemically mobile fraction of most metals was found. In this part of the core, the maximum content of Fe and Mn in the form of authigenic oxy-hydroxides which serve an effective sorbent of most trace elements, including heavy metals, was recorded. At st. 5194, the downcore rythmic covariation of the Si/Al, Ti/Al and Fe/Al ratios reflecting contribution of terrigenous matrix, as well as Al/Ca ratio (indicator of physical and chemical weathering) was revealed. Moreover, the Al/Ca ratio exhibited an asynchronous change with the Si/Al and Fe/Al ratios. Also, the downcore variation in the Ti/Al ratio was opposite to that of Mn/Fe (an indicator of geochemically mobile fraction). Variation of the Ti/Zr ratio, reflecting the range of aerosol transport of clastic material, is weakly expressed in the AMK-5194 core, which supports the proximity of the terrigenous source.


2015 ◽  
Vol 1088 ◽  
pp. 200-205
Author(s):  
Lin Yu ◽  
Dong Wei Li

In this paper analysed the forms of heavy metals (Zn Pb Cd and As) of the Smelting Slag for Lead and Zinc,using BCR sequential extraction. Different chemical morphological of heavy metals have different activity and harmfulness. Migration and Utilization of heavy metals were decided by the existent form of heavy metals in the soil,which influenced Bioactivity and Toxicity. The results show that the main forms of Zn and Cd are Oxidizable and Residual fraction, and Pb mainly occurred in Oxidizable and Reducible fraction. however, As mainly occurred in Residual fraction, which the percentage of reachs 99.56%. According to the percentage of fractions extracted in total content (As is 0.44%, Zn is 14.7%, Pb is 85.98%, Cd is 48.86%),the latent ecological risk of heavy metals varied in the descending order of,Pb Cd Zn and As.


2011 ◽  
Vol 356-360 ◽  
pp. 1733-1738
Author(s):  
Fang He ◽  
Aya Obara ◽  
Shi Long Wang ◽  
Li Guo Wang

The vertical and horizontal distribution of NPEOn and their metabolites of NP and NPEnC in the Upper Nansi Lake, North China were investigated using LC-MS and LC-MS/MS methods, sampling at three sites (St.1, St.2 and St.3) along the water flow direction. The total content of NPEOn (n=1–15) bound onto the sediment of this lake changed in the range of 60.7–631.5 μg/kg-dry with the horizontal flow direction and the vertical direction of the sediment cores with sediment thickness up to 35 cm. Compared to the presence levels of all detected NPEOn species, the content of NP was much higher, falling in 26.5–1,998.4 μg/kg-dry. A general increasing trend of the NP content along the water flow direction of this lake was revealed. NPEnC showed a roughly increasing trend from the upstream to the downstream, with the total concentrations being obviously lower than NPEOn and NP and falling in 2.13–23.1 μg/kg-dry. The short chain NPEOn dominant in NPEO mixtures in these sedimentary cores indicated that this lake received some effluents from STPs, and the sewage treatment ratio is relatively low in this area. Furthermore, the computed magnitudes of NPEO 1-2/NPEO1-15, NP/NPEO 1-15 and NPEC 1-10/NPEO 1-15 suggested that the non-oxidative hydrolytic transformation seemed to be a major process occurring within the sediment phase of Nansi Lake, while the oxidative hydrolytic transformation pathway was probably less involved.


Agronomy ◽  
2020 ◽  
Vol 10 (10) ◽  
pp. 1550
Author(s):  
Elżbieta Malinowska ◽  
Kazimierz Jankowski

The aim of this paper is to evaluate the effect of liming and various doses of municipal sewage sludge (5, 10, and 15% of the weight of the soil) on cobalt total content and its speciation. The incubation experiment lasted 420 days and was conducted in controlled laboratory conditions. Soil was sampled after 30, 60, 90, and 120 days and then, with a break of 180 days, after 360 and 420 days. In all samples, cobalt total content was determined by means of ICP-AES (emission spectrophotometer), and fractions of this metal were measured with the seven-step Zeien and Brümmer method, with seven of them separated: F1–easily soluble, F2–exchangeable, F3–bound to MnOx, F4–bound to organic matter, F5–bound to amorphous FeOx, F6–bound to crystalline FeOx, and F7–residual. Compared to the control, the average content of total cobalt in the soil increased more than two times in experimental units with higher doses of sewage sludge (10% and 15% of the weight of the soil). The metal was mainly bound to the residual fraction, where it constituted 40% of its total content, while in the organic fraction, its share was 20%. In the soil incubated with sludge, cobalt in mobile fractions constituted a small percentage of its total content. Liming limited the release of this metal.


2007 ◽  
Vol 61 (3) ◽  
Author(s):  
T. Frentiu ◽  
S. Vlad ◽  
M. Ponta ◽  
C. Baciu ◽  
I. Kasler ◽  
...  

AbstractThe profile distribution of arsenic(III) and arsenic(V) species in soil and groundwater was investigated in the samples collected in 2005 from a hand-drilled well, in the Bozanta area, Baia Mare region, Romania. The total content of arsenic in the soil was in the range of 525–672 mg kg−1 exceeding 21–27 times the action trigger level for sensitive soil. 0.9–11.3 % of the total content was soluble in water, 83.0–92.6 % in 10 mol dm−3 HCl and 2.6–13.3 % was the residual fraction. Arsenic(V) was the dominant arsenic species in the soil in the range of 405–580 mg kg−1. The distribution and mobility of arsenic species was governed by soil pH and contents of Al, Fe, and Mn. The mobility of arsenic(V) decreased with depth, while that of arsenic(III) was high at the surface and in the proximity of groundwater. The total concentration of arsenic in groundwater was (43.40 ± 1.70) µg dm−3, which exceeded the maximum contaminant level of 10 µg dm−3.


1985 ◽  
Vol 42 (1) ◽  
pp. 23-32 ◽  
Author(s):  
Peter G. C. Campbell ◽  
André Tessier ◽  
Marc Bisson ◽  
René Bougie

Relationships between the partitioning of Cu and Zn in lake sediments and their availability to the yellow water lily, Nuphar variegatum, were examined downstream from a major Cu/Zn mining and smelting complex in Northwestern Quebec, Canada. At each of 13 sampling sites, five N. variegatum individuals were collected, separated into stem and rhizome portions, and analyzed for total Cu and Zn. At the same sites, sediment cores were collected at the base of each plant; the 0- to 2-cm stratum was extruded, wet sieved (850 μm), and subjected to a sequential leaching procedure to determine the partitioning of Cu and Zn among various operationally defined geochemical fractions. Statistical analysis suggested that a significant portion of the Cu burden in N. variegatum was probably derived from the sediments, whereas the Zn content of the plant originated largely in the water column. The concentrations of Cu in the fractions most readily extracted from the sediment were the best indicators of Cu bioavailability in the sediment; normalization of these concentrations with respect to the Fe content of the sediment improved the relationship with [Curhizome], suggesting that Fe may play a protective role in regulating Cu bioavailability.


2019 ◽  
Vol 46 (2) ◽  
pp. 172-177
Author(s):  
D. M. Polyakov ◽  
A. A. Maryash ◽  
A. V. Mozherovsky

The average content of the elements Fe, Mn, Zn, Pb, Cu, Cr, V, Co, Cd, Ni, As, and Mo in the subcolloidal fraction of bottom sediments in the northern and central parts of the Amur Bay (in Russia) was determined. An increase of 5–17% in the content of the metals Pb, Co, Ni, Zn, Cr, V, and As in bottom sediments affected directly by the Razdolnaya River was determined and was found to be associated with sorption on Fe and Mn oxyhydroxides. An increase of 21–55% in the content of the metals Cu and Mo and of the metalloid As compared to their average content in the bottom sediments of the bay was found to be associated with the accumulation by humic substances.


2021 ◽  
Author(s):  
Polina Enchilik ◽  
Ivan Semenkov ◽  
Nikolay Kasimov

Abstract. This study presents a dataset on seasonal soils sampling from September 2016 to May 2018 in the southern part of the Central Forest Reserve (SE Valdai Hills) within a catena with Endocalcaric Albic Glossic Stagnic Profondic Retisols (Cutanic, Loamic) and Albic Gleyic Histic Retisols (Cutanic, Loamic) under coniferous-deciduous forest (Tília cordáta, Pícea ábies, Ácer platanoídes) on loess-like loams underlain by carbonate moraine deposits. 152 soil samples were taken to define total concentration of 67 chemical elements (ChEs), content of three mobile fractions (exchangeable, bound within organo-mineral complexes, bound with Fe and Mn hydroxides) of 69 ChEs and content of residual fraction, including macro elements (Al, Ca, Fe, K, Mg, Mn, Na, P, Ti, S, Si), heavy metals (Ba, Co, Cr, Cu, Ni, Pb, Rb, Sr, Th, U, V, Zn), trace elements (Ag, As, B, Be, Bi, Br, Cd, Cs, Ge, Hf, Li, Mo, Nb, Pd, Sb, Sc, Se, Sn, Ta, Te, Tl,W, Zr) and rare earth elements (Ce, Er, Eu, Gd, La, Lu, Nd, Pr, Sm, Tb, Tm, Dy, Ho, Y, Yb). We measured pH-value, total organic carbon content (TOC), seven particle-size classes (


Land ◽  
2021 ◽  
Vol 11 (1) ◽  
pp. 29
Author(s):  
Alexei Konoplev ◽  
Gennady Laptev ◽  
Yasunori Igarashi ◽  
Hrigoryi Derkach ◽  
Valentin Protsak ◽  
...  

Given the importance of understanding long-term dynamics of radionuclides in the environment in general, and major gaps in the knowledge of 137Cs particulate forms in Chernobyl exclusion zone water bodies, three heavily contaminated water bodies (Lakes Glubokoe, Azbuchin, and Chernobyl NPP Cooling Pond) were studied to reconstruct time changes in particulate concentrations of 137Cs and its apparent distribution coefficient Kd, based on 137Cs depth distributions in bottom sediments. Bottom sediment cores collected from deep-water sites of the above water bodies were sliced into 2 cm layers to obtain 137Cs vertical profile. Assuming negligible sediment mixing and allowing for 137Cs strong binding to sediment, each layer of the core was attributed to a specific year of profile formation. Using this method, temporal trends for particulate 137Cs concentrations in the studied water bodies were derived for the first time and they were generally consistent with the semiempirical diffusional model. Based on the back-calculated particulate 137Cs concentrations, and the available long-term monitoring data for dissolved 137Cs, the dynamics of 137Cs solid–liquid distribution were reconstructed. Importantly, just a single sediment core collected from a lake or pond many years after a nuclear accident seems to be sufficient to retrieve long-term dynamics of contamination.


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