scholarly journals Evaluation of the DGT technique for selective measurement of aluminium and trace metal concentrations in an acid drainage-impacted coastal waterway

2017 ◽  
Vol 19 (5) ◽  
pp. 742-751 ◽  
Author(s):  
Amir Houshang Shiva ◽  
Peter R. Teasdale ◽  
David T. Welsh ◽  
William W. Bennett
Keyword(s):  
Trace Metals ◽  
Trace Metal ◽  
Natural Waters ◽  
Metal Concentrations ◽  
Acid Drainage

DGT samplers with different binding layers (Chelex, Metsorb and mixed Chelex–Metsorb) were evaluated for measurement of Al and trace metals in four natural waters with a range of pH.

scholarly journals Significance of building and plumbing specifics on trace metal concentrations in drinking water

1991 ◽  
Vol 18 (6) ◽  
pp. 893-903 ◽  
Author(s):  
Inderjit Singh ◽  
Donald S. Mavinic
Keyword(s):  
Drinking Water ◽  
Trace Metals ◽  
Trace Metal ◽  
Water Samples ◽  
First Flush ◽  
Single Family ◽  
Metal Concentrations ◽  
Building Height ◽  
High Rise ◽  
Family House

Samples were taken from 72 high-rise apartment suites (6 suites in 12 individual high-rise towers) and 60 single-family houses located within the Greater Vancouver Regional District. The influence of the following factors on trace metal concentrations in 1-L first-flush drinking water samples and “running” hot water samples was investigated: building height, location, plumbing age, type of plumbing, and type of building. Results of this survey show that with the exception of building height, all factors had a correlation with one or more of the trace metals investigated. The trace metals examined were lead, copper, iron, and zinc. Lead was influenced primarily by building type, copper by plumbing age and type of plumbing, and iron by location. Elevated lead levels were associated with high-rise samples. New copper plumbing systems resulted in high copper levels. Highest iron levels in the drinking water were measured in the East Vancouver location. Zinc did not show a distinct correlation with any of the factors investigated. Brass faucets were the primary source of zinc in tap water. They also contributed substantially to the lead detected in the 1-L first-flush sample. Metal concentrations measured in the high-rise and house samples were compared with the U.S. Environmental Protection Agency's (USEPA) maximum contaminant levels (MCLs) and the proposed “no-action” level for lead. In high-rise samples, the 0.01 mg/L “no-action” level proposed for lead was exceeded in 43% of the samples, and 62% of the samples exceeded the current 1.0 mg/L MCL standard for copper. In single-family house samples, these values were 47% and 73%, respectively. The average lead concentrations were 0.020 mg/L for all high-rise samples and 0.013 mg/L for house samples. Regulatory levels stated above would still be exceeded in 6% of the cases for lead and 9% of the cases for copper, even after prolonged flushing of the tap in a high-rise building. In all cases associated with single-family houses, flushing the cold water tap for 5 minutes was successful in achieving compliance levels. Key words: aggressive water, compliance, corrosive, drinking water, first-flush, GVRD, high-rise, single-family house, trace metals, USEPA.

scholarly journals Atmospheric trace metals measured at a regional background site (Welgegund) in South Africa

2017 ◽  
Vol 17 (6) ◽  
pp. 4251-4263 ◽  
Author(s):  
Andrew D. Venter ◽  
Pieter G. van Zyl ◽  
Johan P. Beukes ◽  
Micky Josipovic ◽  
Johan Hendriks ◽  
...  
Keyword(s):  
South Africa ◽  
Trace Metals ◽  
Trace Metal ◽  
Size Fraction ◽  
Abundant Species ◽  
Metal Species ◽  
Metal Concentrations ◽  
Igneous Complex ◽  
Size Fractions ◽  
Bushveld Igneous Complex

Abstract. Atmospheric trace metals can cause a variety of health-related and environmental problems. Only a few studies on atmospheric trace metal concentrations have been conducted in South Africa. Therefore the aim of this study was to determine trace metal concentrations in aerosols collected at a regional background site, i.e. Welgegund, South Africa. PM1, PM1–2. 5 and PM2. 5–10 samples were collected for 13 months, and 31 atmospheric trace metal species were detected. Atmospheric iron (Fe) had the highest concentrations in all three size fractions, while calcium (Ca) was the second-most-abundant species. Chromium (Cr) and sodium (Na) concentrations were the third- and fourth-most-abundant species, respectively. The concentrations of the trace metal species in all three size ranges were similar, with the exception of Fe, which had higher concentrations in the PM1 size fraction. With the exception of titanium (Ti), aluminium (Al) and manganese (Mg), 70 % or more of the trace metal species detected were in the smaller size fractions, which indicated the influence of industrial activities. However, the large influence of wind-blown dust was reflected by 30 % or more of trace metals being present in the PM2. 5–10 size fraction. Comparison of trace metals determined at Welgegund to those in the western Bushveld Igneous Complex indicated that at both locations similar species were observed, with Fe being the most abundant. However, concentrations of these trace metal species were significantly higher in the western Bushveld Igneous Complex. Fe concentrations at the Vaal Triangle were similar to levels thereof at Welgegund, while concentrations of species associated with pyrometallurgical smelting were lower. Annual average Ni was 4 times higher, and annual average As was marginally higher than their respective European standard values, which could be attributed to regional influence of pyrometallurgical industries in the western Bushveld Igneous Complex. All three size fractions indicated elevated trace metal concentrations coinciding with the end of the dry season, which could partially be attributed to decreased wet removal and increases in wind generation of particulates. Principal component factor analysis (PCFA) revealed four meaningful factors in the PM1 size fraction, i.e. crustal, pyrometallurgical-related and Au slimes dams. No meaningful factors were determined for the PM1–2. 5 and PM2. 5–10 size fractions, which was attributed to the large influence of wind-blown dust on atmospheric trace metals determined at Welgegund. Pollution roses confirmed the influence of wind-blown dust on trace metal concentrations measured at Welgegund, while the impact of industrial activities was also substantiated.

A 50-yr Record of Pollution by Nutrients, Trace Metals, and Organic Chemicals in the St Lawrence River

1994 ◽  
Vol 51 (5) ◽  
pp. 1088-1100 ◽  
Author(s):  
Richard Carignan ◽  
Stéphane Lorrain ◽  
Ken Lum
Keyword(s):  
Trace Metals ◽  
Trace Metal ◽  
Organic Contaminants ◽  
River Discharge ◽  
Organic Chemicals ◽  
Metal Concentrations ◽  
Organic C ◽  
Pcb Congeners ◽  
Anthropogenic Inputs ◽  
St Lawrence River

The deposition chronology of algal pigments, organic C, N, P, trace metals, and organic contaminants (PCB congeners, DDD, DDE, Mirex, hexachlorobenzene) is described for two sites in fluvial lakes (St. Francis and St. Louis) of the St. Lawrence River. Pigment concentrations rapidly decrease in the top 10 cm due to degradation, but show a broad secondary peak consistent with higher primary productivity between 1960 and 1975. In Lake St. Francis, deposition of organic C, N, and P peaked between 1950 and 1975. In both lakes, trace metal concentrations reached maximum values between 1960 and 1970 and decreased considerably between 1970 and 1980. At both sites, surficial trace metal concentrations are approaching (within a factor of 3) those observed in preindustrial sediments except Cd, which is still 5–6 times higher. Concentrations of Cr, Cu, Ni, and Zn are inversely related (p < 0.05) to river discharge whereas those of Pb are positively related to discharge. Concentrations of organic contaminants have declined by a factor of 5–10 between the mid-1960's and the early 1980's, except Mirex, which shows no obvious trend with time. Historic trends in pollution by organic chemicals appear to have been influenced not only by changing anthropogenic inputs, but also by river discharge.

Sampling techniques for reliable determination of trace metals in macrophytes and periphyton

1995 ◽  
Vol 46 (7) ◽  
pp. 1047
Author(s):  
TP McBride ◽  
BN Noller
Keyword(s):  
Trace Metals ◽  
Trace Metal ◽  
Submerged Macrophytes ◽  
Dry Weight ◽  
Total Sample ◽  
Flood Plain ◽  
Sampling Techniques ◽  
Metal Concentrations ◽  
Reliable Determination

Sampling techniques were developed to measure trace-metal concentrations reliably in the shoots of a submerged macrophyte, Najas tenuifolia, and its attached periphyton growing in the Magela Creek flood plain in monsoonal northern Australia. At each site, 30 samples were collected within an 8-m by 8-m quadrat in a pattern of five samples from each of six irregularly spaced points. Samples were collected underwater to include all periphyton present, and precautions were taken at all stages of processing to avoid contamination. Periphyton was dislodged for separate chemical analysis by sonication followed by vigorous shaking. A significant aspect was the large amount of periphyton, up to 35% of the total sample dry weight, associated with the Najas sp. Only a proportion, up to 43%, of this periphyton could be dislodged by the physical procedures used. Trace metals were generally not present in the same concentrations in both the Najas sp. and the periphyton. The average trace-metal concentrations (μg g-1 dry weight) and standard errors measured in the Najas sp. (and periphyton) were cadmium 0.24 � 0.013 (0.093 � 0.012), copper 5.2� 0.25 (12 � 0.74), lead 0.93 � 0.084 (6.5 � 0.43), manganese 2500 � 110 (1500 � 110), uranium 0.24 � 0.023 (0.27 � 0.030), and zinc 38 � 1.0 (23 � 1.5). The significant differences in Najas sp. and periphyton trace-metal concentrations show the need to consider the effect of periphyton when sampling and reporting trace-metal concentrations in submerged macrophytes.

scholarly journals Metal contamination and oxidative stress biomarkers in estuarine fish following a mine tailing disaster

2020 ◽  
Author(s):  
Fabrício Ângelo Gabriel ◽  
Rachel Ann Hauser-Davis ◽  
Lorena Oliveira Souza Soares ◽  
Ana Carolina de Azevedo Mazzuco ◽  
Rafael Christian Chávez Rocha ◽  
...  
Keyword(s):  
Trace Metals ◽  
Trace Metal ◽  
Muscle Tissue ◽  
Fish Species ◽  
Metal Contamination ◽  
Contaminated Sediments ◽  
Estuarine Sediments ◽  
Estuarine Fish ◽  
Human Consumption ◽  
Metal Concentrations

AbstractThe Rio Doce estuary in Brazil was impacted by the deposition of mine tailings caused by the collapse of a mining dam in 2015. Since the disaster, the estuary is experiencing chronic trace metal contamination effects, but potential trace metal accumulation in fishes has not been reported. Trace metals in aquatic ecosystems pose severe threats to the aquatic biota, so we hypothesized that the accumulation of trace metals in estuarine sediments nearly two years after the disaster would cause contaminant bioaccumulation, resulting in the biosynthesis of metal-responsive proteins in fishes. We determined trace metal concentrations in sediment samples, metal concentrations, and quantified stress protein concentrations in the liver and muscle tissue of five different fish species in the estuary. Our results revealed high concentrations of trace metals in estuarine sediments when compared to published baseline values for this estuary. The demersal fish species Cathorops spixii and Genidens genidens had the highest Hg, As, Se, Cr, and Mn concentrations in both hepatic and muscle tissues. Metal bioaccumulation in fish was statistically correlated with the biosynthesis of metallothionein and reduced glutathione in both fish liver and muscle tissue. The trace metals detected in fish tissues resemble those in the contaminated sediments present at the estuary at the time of this study and were also significantly correlated to protein levels. Trace metals in fish muscle were above the maximum permissible limits for human consumption, suggesting potential human health risks that require further determination. Our study supports the high biogeochemical mobility of trace metals between contaminated sediments and local biota in estuarine ecosystems.

scholarly journals Trace Metal Dynamics in Shallow Hydrothermal Plumes at the Kermadec Arc

2022 ◽  
Vol 8 ◽  
Author(s):  
Charlotte Kleint ◽  
Rebecca Zitoun ◽  
René Neuholz ◽  
Maren Walter ◽  
Bernhard Schnetger ◽  
...  
Keyword(s):  
Trace Metals ◽  
Trace Metal ◽  
Water Depth ◽  
Hydrothermal Vents ◽  
Fluid Composition ◽  
Data Set ◽  
Metal Concentrations ◽  
Hydrothermal Plumes ◽  
Particle Adsorption ◽  
Dissolved Trace Metals

Hydrothermal vents are a source of many trace metals to the oceans. Compared to mid-ocean ridges, hydrothermal vent systems at arcs occur in shallower water depth and are much more diverse in fluid composition, resulting in highly variable water column trace metal concentrations. However, only few studies have focused on trace metal dynamics in hydrothermal plumes at volcanic arcs. During R/V Sonne cruise SO253 in 2016/2017, hydrothermal plumes from two hydrothermally active submarine volcanoes along the Kermadec arc in the Southwest Pacific Ocean were sampled: (1) Macauley, a magmatic dominated vent site located in water depths between 300 and 680 m, and (2) Brothers, located between 1,200 and 1,600 m water depth, where hydrothermalism influenced by water rock interactions and magmatically influenced vent sites occur near each other. Surface currents estimated from satellite-altimeter derived currents and direct measurements at the sites using lowered acoustic Doppler current profilers indicate the oceanic regime is dominated by mesoscale eddies. At both volcanoes, results indicated strong plumes of dissolved trace metals, notably Mn, Fe, Co, Ni, Cu, Zn, Cd, La, and Pb, some of which are essential micronutrients. Dissolved metal concentrations commonly decreased with distance from the vents, as to be expected, however, certain element/Fe ratios increased, suggesting a higher solubility of these elements and/or their stronger stabilization (e.g., for Zn compared to Fe). Our data indicate that at the magmatically influenced Macauley and Brothers cone sites, the transport of trace metals is strongly controlled by sulfide nanoparticles, while at the Brothers NW caldera wall site iron oxyhydroxides seem to dominate the trace metal transport over sulfides. Solution stabilization of trace metals by organic complexation appears to compete with particle adsorption processes. As well as extending the generally sparse data set for hydrothermal plumes at volcanic arc systems, our study presents the first data on several dissolved trace metals in the Macauley system, and extends the existing plume dataset of Brothers volcano. Our data further indicate that chemical signatures and processes at arc volcanoes are highly diverse, even on small scales.

scholarly journals Contamination and oxidative stress biomarkers in estuarine fish following a mine tailing disaster

PeerJ ◽  
2020 ◽  
Vol 8 ◽  
pp. e10266 ◽  
Author(s):  
Fabrício Â. Gabriel ◽  
Rachel Ann Hauser-Davis ◽  
Lorena Soares ◽  
Ana Carolina A. Mazzuco ◽  
Rafael Christian Chavez Rocha ◽  
...  
Keyword(s):  
Trace Metals ◽  
Trace Metal ◽  
Human Health ◽  
Health Risks ◽  
Fish Species ◽  
Reduced Glutathione ◽  
Estuarine Sediments ◽  
Metal Concentrations ◽  
Human Health Risks ◽  
Muscle Tissues

Background The Rio Doce estuary, in Brazil, was impacted by the deposition of iron mine tailings, caused by the collapse of a dam in 2015. Based on published baseline datasets, the estuary has been experiencing chronic trace metal contamination effects since 2017, with potential bioaccumulation in fishes and human health risks. As metal and metalloid concentrations in aquatic ecosystems pose severe threats to the aquatic biota, we hypothesized that the trace metals in estuarine sediments nearly two years after the disaster would lead to bioaccumulation in demersal fishes and result in the biosynthesis of metal-responsive proteins. Methods We measured As, Cd, Cr, Cu, Fe, Mn, Pb, Se and Zn concentrations in sediment samples in August 2017 and compared to published baseline levels. Also, trace metals (As, Cd, Cr, Cu, Fe, Hg, Mn, Pb, Se and Zn) and protein (metallothionein and reduced glutathione) concentrations were quantified in the liver and muscle tissues of five fish species (Cathorops spixii, Genidens genidens, Eugerres brasilianus, Diapterus rhombeus and Mugil sp.) from the estuary, commonly used as food sources by local populations. Results Our results revealed high trace metal concentrations in estuarine sediments, when compared to published baseline values for the same estuary. The demersal fish species C. spixii and G. genidens had the highest concentrations of As, Cr, Mn, Hg, and Se in both, hepatic and muscle, tissues. Trace metal bioaccumulation in fish was correlated with the biosynthesis of metallothionein and reduced glutathione in both, liver and muscle, tissues, suggesting active physiological responses to contamination sources. The trace metal concentrations determined in fish tissues were also present in the estuarine sediments at the time of this study. Some elements had concentrations above the maximum permissible limits for human consumption in fish muscles (e.g., As, Cr, Mn, Se and Zn), suggesting potential human health risks that require further studies. Our study supports the high biogeochemical mobility of toxic elements between sediments and the bottom-dwelling biota in estuarine ecosystems.

A suitable model for the biomonitoring of trace metal bioavailabilities in estuarine sediments: the annelid polychaete Nereis diversicolor

2006 ◽  
Vol 86 (1) ◽  
pp. 71-82 ◽  
Author(s):  
Laurence Poirier ◽  
Brigitte Berthet ◽  
Jean-Claude Amiard ◽  
Anne-Yvonne Jeantet ◽  
Claude Amiard-Triquet
Keyword(s):  
Trace Metals ◽  
Trace Metal ◽  
Metal Contamination ◽  
Estuarine Sediments ◽  
Suitable Model ◽  
English Channel ◽  
Metal Concentrations ◽  
Trace Metal Contamination ◽  
Nereis Diversicolor ◽  
Total Sediment

The need to use biomonitors representative of the sedimentary compartment has been recognized, particularly in estuaries. Thus, trace metal contamination has been monitored in an infaunal polychaete worm Nereis diversicolor and sediments in the Seine estuary and comparatively in the relatively clean Authie estuary (French coast of the English Channel) over two years taking samples every three months at both sites. No correlations were shown between total metal (Ag, Cd, Cu, Pb, Zn) concentrations in raw sediments and ragworms. Because these worms are known to be good biomonitors of the bioavailabilities of sedimentary trace metals, it follows that total sediment metal concentrations have a poor predictive ecotoxicological value. Using a correction factor to minimize the influence of weight, it is possible to make a good estimation of the average metal concentrations in a population of worms at a given site, sampling only a limited number of specimens. Metallothioneins are often considered to be good biomarkers of the presence of significant availabilities of trace metals. Metallothionein-like proteins (MTLPs) are present in N. diversicolor, but there is no significant relationship between MTLPs and metal concentrations. This situation might result from the importance of metal-containing granules, both extra- and intracellular, in ragworms.

Complexation of Lead in Model Solutions of Humic Acid: Heterogeneity and Effects of Competition with Copper, Nickel, and Zinc

2006 ◽  
Vol 3 (4) ◽  
pp. 276 ◽  
Author(s):  
Ismail I. Fasfous ◽  
C. L. Chakrabarti ◽  
John Murimboh ◽  
Tahir Yapici
Keyword(s):  
Humic Acid ◽  
Trace Metals ◽  
Trace Metal ◽  
Humic Substances ◽  
Metal Concentration ◽  
Natural Waters ◽  
Metal Bioavailability ◽  
Copper Nickel ◽  
Model Solutions ◽  
Equilibrium Function

Environmental Context. Metal bioavailability and toxicity are often related to free metal concentration rather than total metal concentration. Humic substances are chemically and physically heterogeneous complexants for metals in natural waters, and play an important role in trace metal transport, fate, and bioavailability. Metal bioavailability, which depends on chemical speciation of metals, is greatly influenced by the presence of other trace metals and major cations in natural waters. In this work, the effects of heterogeneity of humic substances, and of competition of trace metals on lead speciation in model solutions have been studied to gain a better understanding of these effects on complexation of trace metal lead and its bioavailability. Abstract. Physicochemical heterogeneity of a well characterized humic acid (HA) in its complexation with a trace metal lead in model solutions was investigated using pseudo-polarography at a stationary mercury drop electrode, and the differential equilibrium function (DEF) of Pb(ii)–HA complexes was determined. The complexation of Pb(ii) by HA was determined by taking into account the dependence of the strength of the binding on the metal (Pb) loading. Also investigated were the effects of competition of the trace metals copper, nickel, and zinc on the DEF of Pb(ii)–HA complexes in model solutions. The results showed that these trace metals competed with trace metal lead for binding by HA even when present at the same concentrations as that of lead.

Trace metal speciation in the Yamaska and St. François Rivers (Quebec)

1980 ◽  
Vol 17 (1) ◽  
pp. 90-105 ◽  
Author(s):  
A. Tessier ◽  
P. G. C. Campbell ◽  
M. Bisson
Keyword(s):  
Organic Matter ◽  
Trace Metals ◽  
Trace Metal ◽  
Suspended Sediment ◽  
Extraction Procedure ◽  
Municipal Sewage ◽  
Residual Fraction ◽  
Metal Concentrations ◽  
Sediment Samples ◽  
Mn Oxides

Water and suspended sediment samples were collected at 12 stations on the Yamaska and St. François Rivers, located in southeastern Quebec, and were analyzed for the trace metals Cd, Co, Cu, Ni, Pb, Zn, Fe, and Mn. The suspended sediment samples were subjected to a sequential extraction procedure designed to partition the particulate trace metals into five fractions: (1) exchangeable; (2) bound to carbonates; (3) bound to Fe–Mn oxides; (4) bound to organic matter; and (5) residual.Although suspended sediment levels as well as total soluble and particulate trace metal concentrations were highly variable in time and space, speciation patterns for each metal proved reasonably constant. Very small proportions of all metals, except Cd and Mn, were found in the exchangeable fraction, whereas high levels of all metals were present in the residual fraction; Fe–Mn oxides and organic matter constituted important transport phases for most metals. Deviations from this general behaviour were occasioned by man-induced perturbations (e.g., inputs of municipal sewage or mine waste water). At stations influenced by such factors, total particulate metal concentrations increased and the relative contribution of the residual fraction decreased. The trace metal content of fraction 3 proved to be particularly sensitive to anthropogenic inputs; other phases acting as trace metal sinks included those liberated in fractions 1 (Cd, Cu, Ni, Zn), 2(Cu, Ni, Zn), and 4(Cu, Ni).

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