Observational studies have indicated that low-to-moderate exposure to cadmium (Cd), lead (Pb), and mercury (Hg) adversely affects birth anthropometry, but results are inconclusive. The aim of this study was to elucidate potential impact on birth anthropometry of exposure to Cd, Pb, and Hg in pregnant women, and to identify the main dietary sources. In the NICE (Nutritional impact on Immunological maturation during Childhood in relation to the Environment) birth-cohort in northern Sweden, blood and urine were collected from pregnant women in early third trimester. Cd, Pb and Hg were measured in erythrocytes (n = 584), and Cd also in urine (n = 581), by inductively coupled plasma mass spectrometry. Dietary data were collected through a semi-quantitative food frequency questionnaire administered in mid-third trimester. Birth anthropometry data were extracted from hospital records. In multivariable-adjusted spline regression models, a doubling of maternal erythrocyte Cd (median: 0.29 μg/kg) above the spline knot of 0.50 μg/kg was associated with reduced birth weight (B: −191 g; 95% CI: −315, −68) and length (−0.67 cm; −1.2, −0.14). The association with birth weight remained when the analysis was restricted to never-smokers. Likewise, a doubling of erythrocyte Hg (median 1.5 μg/kg, mainly MeHg) above 1.0 μg/kg, was associated with decreased birth weight (−59 g; −115, −3.0), and length (−0.29 cm; −0.54, −0.047). Maternal Pb (median 11 μg/kg) was unrelated to birth weight and length. Erythrocyte Cd was primarily associated with intake of plant derived foods, Pb with game meat, tea and coffee, and Hg with fish. The results indicated that low-level maternal Cd and Hg exposure were associated with poorer birth anthropometry. Further prospective studies in low-level exposed populations are warranted.

Particulate air pollution in cities comprises a variety of harmful compounds, including fine iron rich particles, which can persist in the air for long time, increasing the adverse exposure of humans and living things to them. We studied street tree (among other species, Cordyline australis, Fraxinus excelsior and F. pensylvanica) barks as biological collectors of these ubiquitous airborne particles in cities. Properties were determined by the environmental magnetism method, inductively coupled plasma optical emission spectrometry and scanning electron microscopy, and analyzed by geostatistical methods. Trapped particles are characterized as low-coercivity (mean ± s.d. value of remanent coercivity Hcᵣ = 37.0 ± 2.4 mT) magnetite-like minerals produced by a common pollution source identified as traffic derived emissions. Most of these Fe rich particles are inhalable (PM₂.₅), as determined by the anhysteretic ratio χARM/χ (0.1–1 μm) and scanning electron microscopy (<1 μm), and host a variety of potentially toxic elements (Cr, Mo, Ni, and V). Contents of magnetic particles vary in the study area as observed by magnetic proxies for pollution, such as mass specific magnetic susceptibility χ (18.4–218 × 10⁻⁸ m³ kg⁻¹) and in situ magnetic susceptibility κᵢₛ (0.2–20.2 × 10⁻⁵ SI). The last parameter allows us doing in situ magnetic biomonitoring, being convenient because of species preservation, measurement time, and fast data processing for producing prediction maps of magnetic particle pollution.

With the constant quest for new sources of superfoods to supplement the largely nutrient deficient diet of the modern society, sea cucumbers are gaining increasing popularity. Three species of sea cucumbers, Cucumaria frondosa, Apostichopus californicus and Apostichopusjaponicus were collected from three geographical regions, Atlantic and Pacific coast of Canada and Yellow sea/ East China sea in China, respectively. These organisms were sectioned into parts (body wall, tentacles, internal organ, skin and muscle) and analysed for total arsenic (As) by inductively coupled plasma mass spectrometry (ICP-MS) and As species by high-performance liquid chromatography (HPLC) coupled to ICP-MS. Normal and reversed sequential extractions were optimised to address As distribution between lipids (polar and non-polar) and water-extractable fractions. Two extraction methods for water-extractable As were compared in terms of the number and the amount of extracted species. The results revealed that total As concentration and As species distribution varies significantly between sea cucumbers species. Total As in studied body parts ranged between 2.8 ± 0.52 and 7.9 ± 1.2 mg kg⁻¹, with an exception of the muscle tissue of A. californicus, where it reached to 36 ± 3.5 mg kg⁻¹. Arsenobetaine (AsB) was the most abundant As species in A. californicus and A.japonicus, however, inorganic As represented over 70% of total recovered As in the body parts of C. frondosa. Arsenosugars-328 and 482 were found in all studied body parts whereas arsenosugar-408 was only found in the skin of A. californicus. This is the first time that such a variation in As species distribution between sea cucumber species has been shown.

The exposure risk of metal-based nanoparticles (NPs) to marine organisms and related food safety have attracted increasing attention, but the actual concentrations of these NPs in seawater and marine organisms are unknown. In this work, single particle inductively coupled plasma-mass spectrometry (spICP-MS) was used to quantify the concentrations and size distributions of NPs in different marine mollusks (oysters, mussels, scallops, clams, and ark shells) from an offshore aquaculture farm. Results showed that Ti, Cu, Zn, and Ag bearing NPs were detected in all the five mollusks with the mean sizes at 65.4–70.9, 72.2–89.6, 97.8–108.3, and 42.9–51.0 nm, respectively. The particle concentrations of Ti, Cu, Zn, and Ag bearing NPs in all mollusks (0.88–3.26 × 10⁷ particles/g fresh weight) were much higher than that in the seawater (0.46–0.79 × 10⁷ particles/mL), suggesting bio-accumulation of NPs. For all the five mollusks, Ag bearing NPs had the highest number-based bioconcentration factors (NBCFs) in all the tested NPs due to the smallest mean size of Ag bearing NPs in seawater (30.5 nm). In addition, the clams exhibited the lowest NBCFs of the four NPs than other mollusks. All four NPs were mainly accumulated in the gill and digestive gland, and could transfer to adductor muscle of all mollusks. Although all the four metals (Ti, Cu, Zn, Ag) in mollusks were safe for human consumption by the estimated daily intake (EDI) analysis, the risk of NPs remaining in the mollusks should be further considered when evaluating the toxicity of metals for human health. The findings could improve our understanding on the distribution and health risk of NPs in marine mollusks under offshore aquaculture.

Marine fishes are exposed to great human-induced alterations due to the indiscriminate discharges into the sea, increasing marine pollution. For this study, 324 specimens of Sardina pilchardus from the Canary Islands were analized during a period of 2 years (June 2016 to May 2018). The concentration of 11 metals and trace elements (Al, B, Cd, Cr, Cu, Fe, Li, Ni, Pb, V and Zn) was determined in each individual using the Inductively Coupled Plasma Optical Emission Spectrometry (ICP-OES) technique. Statistical analyses were carried out considering the following factors: oceanographic season, maturity of the gonads in the seasons, size of the specimens. Sardina pilchardus specimens captured in the hot season presented higher Ni, Li and Pb levels than the specimens caught in the cold season. Immature specimens had higher concentration in more metals than the mature specimens. This fact may be due to the fact that these specimens require a much higher metabolic rate due to their growth and do not detoxify like mature specimens. Significant differences were found in the concentration of metals in all the analyzes performed.

This work presents the results of a PM2.5 source apportionment study conducted in urban background sites from 16 European and Asian countries. For some Eastern Europe and Central Asia cities this was the first time that quantitative information on pollution source contributions to ambient particulate matter (PM) has been performed. More than 2200 filters were sampled and analyzed by X-Ray Fluorescence (XRF), Particle-Induced X-Ray Emission (PIXE), and Inductively Coupled Plasma Mass Spectrometry (ICP-MS) to measure the concentrations of chemical elements in fine particles. Samples were also analyzed for the contents of black carbon, elemental carbon, organic carbon, and water-soluble ions. The Positive Matrix Factorization receptor model (EPA PMF 5.0) was used to characterize similarities and heterogeneities in PM2.5 sources and respective contributions in the cities that the number of collected samples exceeded 75. At the end source apportionment was performed in 11 out of the 16 participating cities. Nine major sources were identified to have contributed to PM2.5: biomass burning, secondary sulfates, traffic, fuel oil combustion, industry, coal combustion, soil, salt and “other sources”. From the averages of sources contributions, considering 11 cities 16% of PM2.5 was attributed to biomass burning, 15% to secondary sulfates, 13% to traffic, 12% to soil, 8.0% to fuel oil combustion, 5.5% to coal combustion, 1.9% to salt, 0.8% to industry emissions, 5.1% to “other sources” and 23% to unaccounted mass. Characteristic seasonal patterns were identified for each PM2.5 source. Biomass burning in all cities, coal combustion in Krakow/POL, and oil combustion in Belgrade/SRB and Banja Luka/BIH increased in Winter due to the impact of domestic heating, whereas in most cities secondary sulfates reached higher levels in Summer as a consequence of the enhanced photochemical activity. During high pollution days the largest sources of fine particles were biomass burning, traffic and secondary sulfates.

Interaction between silver nanoparticles (AgNPs) and iron plaque, which forms at the root surface of wetland plants under waterlogging conditions, is a critical process that controls the bioavailability of AgNPs. In this study, we comparatively evaluated how and to what extent iron plaque affected silver uptake sourced from metallic (Ag⁰NPs) and sulfidized (Ag₂S-NPs) silver nanoparticles under hydroponic conditions. After the formation of iron plaque at the root surface upon exposure to Fe²⁺ at 0–100 μg mL⁻¹, rice (Oryza sativa L.) seedlings were transferred to AgNP suspensions. Silver uptake depended on the amount of iron plaque and AgNP species (Ag⁰NPs vs. Ag₂S-NPs): Ag₂S-NP exposure had lower or comparable Ag uptake to that of Ag⁰NP exposure at low levels of Fe²⁺ (0–80 μg mL⁻¹), but significantly higher Ag uptake at 100 μg Fe²⁺ mL⁻¹. Such contrasting effects of iron plaque on the bioavailability of Ag⁰NPs and Ag₂S-NPs were attributed to their influences on AgNP dissolution. However, the translocation factors (TFs) and particle size distribution of NPs in planta (as determined by single-particle inductively coupled plasma-mass spectrometry analysis) were not affected by the amount of iron plaque. These results reveal contrasting effects of iron plaque on the bioavailability of Ag⁰NPs and Ag₂S-NPs, and raise concerns about the exposure of wetland plants to Ag₂S-NPs in Fe-rich environments, where high Fe levels may facilitate Ag₂S-NP bioavailability.

Metal pollution in the Bohai Sea in China has posed a potential risk on marine organisms. In this work, crabs (Portunus trituberculatus) were sampled from four sites, namely a reference (site 3934) and three metal-polluted (sites 6151, 6351, and 3562) sites, located in the Bohai Sea. Metal concentrations in crab gill tissues were measured using inductively coupled plasma mass spectrometry. Cu, Zn, and Cd in crab samples from S3562 presented the highest concentrations. Particularly, Cu concentration exceeded the marine biological quality standard II. Cd contents in crab samples from all metal-polluted sites exceeded the marine biological quality standard I. Nuclear magnetic resonance-based metabolomics indicated metal pollution-induced immune stresses in crab samples from all metal-polluted sites. Metal pollution in S6151 and S6351 disturbed energy metabolism through differential pathways. For crab samples from S3562, the metabolic profile suggested that metal pollution mainly induced osmotic stress.

In this present paper, the distribution of toxic metals and sediment quality were evaluated in five sampling points of the Itapicuru-Mirim River located in the city of Jacobina, Bahia, Brazil. The concentration of the elements arsenic (As), cadmium (Cd), chromium (Cr), copper (Cu), iron (Fe), mercury (Hg), manganese (Mn), nickel (Ni), lead (Pb), and zinc (Zn) were determined from sediment samples collected from the superficial layer (0–10 cm) in November 2013. After the samples' total decomposition, the total concentration of metals was determined by inductively coupled plasma optical emission spectrometry (ICP OES), except for Hg, which was measured by inductively coupled plasma atomic emission spectrometry (ICP AES). A geochemical evaluation of sediment quality was performed using enrichment factor (EF), geoaccumulation index (Igₑₒ), and pollution load index (PLIThe results of the total concentrations in the analyzed sediment samples were compared with the threshold effect levels (TELs) and probable (PELs) effect levels (PELs) in sediment quality guidelines (SQGs). For the fraction <75 μm, the decreasing order for the metal concentrations was (ppm): Fe (10.86%) > Mn (120.8) > Cr (122) > Zn (76.5) > Pb (49.6) > Cu (32.6) > Ni (28.6) > Hg (0.31) > Cd (0.13). Igₑₒ suggested a moderate to seriously polluted category for Hg and moderately polluted for Cu. Generally, the results indicated probable risks to the biota caused by Cr, Ni, Pb, and Hg metals. However, only Hg, Cd, and Cu were of anthropogenic origin. Although the sediments are relatively preserved from pollution by these metals, there is a progressive deterioration of this compartment downstream of the Itapicuru-Mirim River in the city of Jacobina.

The distribution characteristics, correlation, and bioavailability of 14 trace elements in different fishes and corals collected from the coral-reef systems of the Xisha Islands, China were systematic studied for the first time. All detected elements were measured using inductively coupled plasma mass spectrometry after pretreatment by microwave digestion. The fishes had slight differences in element enrichment selectivity and bioavailability with average levels as follows: V, 0.100 mg·kg⁻¹; Cr, 0.683 mg·kg⁻¹; Mn, 1.178 mg·kg⁻¹; Fe, 51.806 mg·kg⁻¹; Co, 0.072 mg·kg⁻¹; Ni, 1.286 mg·kg⁻¹; Cu, 1.428 mg·kg⁻¹; Zn, 10.384 mg·kg⁻¹; As, 6.437 mg·kg⁻¹; Se, 0.830 mg·kg⁻¹; Mo, 0.101 mg·kg⁻¹; Cd, 0.051 mg·kg⁻¹; Pb, 0.308 mg·kg⁻¹; and U, 0.008 mg·kg⁻¹. Trace element contents in corals were higher than those in fishes. The distribution characteristics of trace elements in fishes and corals presented a significant correlation in North Reef and Yongle Atoll, thereby indicating an evident effect on living areas compared with trace elements in fishes from the Spratly Islands. Cluster analysis of fishes and corals based on trace elements showed that they had different selectivities and bioavailabilities to trace elements. The EDI and THQ ratios of Cu, As, Cd, Cr, and Pb demonstrated that fishes were unlikely to experience serious adverse effects, except for As in Chaetodon auriga, Myripristis kuntee, Gnathodentex aureolineatus, and Hemigymnus melapterus in Xisha Islands.