Comparison of the levels of organic, elemental and inorganic carbon in particulate matter in six urban environments in Europe

International audienceA series of 7-week sampling campaigns were conducted in urban background sites in the six European cities as follows: Duisburg 4 October?21 November 2002 (autumn), Prague 29 November 2002?16 January 2003 (winter), Amsterdam 24 January?13 March 2003 (winter), Helsinki 21 March?12 May 2003 (spring), Barcelona 28 March?19 May 2003 (spring) and Athens 2 June?21 July 2003 (summer). The campaigns were scheduled to include seasons of local public health concern due to high PM concentrations or findings in previously conducted epidemiological studies. Aerosol samples were collected in parallel with two identical virtual impactors (VI), which divide air PM into two size fractions, PM2.5 and PM2.5-10. The filter samples were analysed with a microbalance, an energy dispersive X-ray fluorescence (ED-XRF), an ion chromatograph (IC) and a thermo-optical carbon analyser (TOA). The PM2.5 and PM2.5-10 campaign means ranged 8.3?29.6 µg m-3 and 5.4?28.7 µg m-3, respectively. The ''wet and cool'' seasons favoured low coarse PM concentration and high fine PM concentration, whereas the spring and summer led to low fine and high coarse PM concentrations. The contribution of particulate organic matter (POM) to PM2.5-10 was highest (27%) in Prague and the lowest (10%) in Barcelona, while those to PM2.5 were generally higher, ranging from 21% in Barcelona to 54% in Prague. The contribution of elemental carbon (EC) to PM2.5-10 were relatively low (1?6%) in all the six European cities but it contributed somewhat higher (5?9%) to PM2.5. The differences are most likely due to variable contributions of local emission sources and seasonal factors such as domestic heating, vehicle exhausts and photochemical reactions. Carbonate, which interferes with carbon analysis by evolving stage at 900°C, was detected in the coarse particles of Athens and Barcelona and it could be separated reliably from OC by a simple integrating method. The calcium carbonate in Athens and Barcelona accounted for 56% and 11% of coarse PM masses, respectively. Carbonate was not found in other cities or in PM2.5. The mean PM2.5 mass portions of five OC thermal fractions (OC1, OC2, OC3, OC4 and OCP) varied in the range 26?33%, 6?10%, 7?10%, 9?22% and 29?50%, respectively, in six cities. The differences in the mass portion profiles were relatively small between the cities

Organic, elemental and inorganic carbon in particulate matter of six urban environments in Europe

International audienceA series of 7-week sampling campaigns were conducted in urban background sites of six European cities as follows: Duisburg (autumn), Prague (winter), Amsterdam (winter), Helsinki (spring), Barcelona (spring) and Athens (summer). The campaigns were scheduled to include seasons of local public health concern due to high particulate concentrations or findings in previously conducted epidemiological studies. Aerosol samples were collected in parallel with two identical virtual impactors that divide air particles into fine (PM2.5) and coarse (PM2.5-10) size ranges. From the collected filter samples, elemental (EC) and organic (OC) carbon contents were analysed with a thermal-optical carbon analyser (TOA); total Ca, Ti, Fe, Si, Al and K by energy dispersive X-ray fluorescence (ED-XRF); As, Cu, Ni, V, and Zn by inductively coupled plasma mass spectrometry (ICP/MS); Ca2+, succinate, malonate and oxalate by ion chromatography (IC); and the sum of levoglucosan+galactosan+mannosan (?MA) by liquid chromatography mass spectrometry (LC/MS). The campaign means of PM2.5 and PM2.5-10 were 8.3-29.6 µg m-3 and 5.4-28.7 µg m-3, respectively. The contribution of particulate organic matter (POM) to PM2.5 ranged from 21% in Barcelona to 54% in Prague, while that to PM2.5-10 ranged from 10% in Barcelona to 27% in Prague. The contribution of EC was higher to PM2.5 (5-9%) than to PM2.5-10 (1-6%) in all the six campaigns. Carbonate (C(CO3), that interferes with the TOA analysis, was detected in PM2.5-10 of Athens and Barcelona but not elsewhere. It was subtracted from the OC by a simple integration method that was validated. The CaCO3 accounted for 55% and 11% of PM2.5-10 in Athens and Barcelona, respectively. It was anticipated that combustion emissions from vehicle engines affected the POM content in PM2.5 of all the six sampling campaigns, but a comparison of mass concentration ratios of the selected inorganic and organic tracers of common sources of organic material to POM suggested also interesting differences in source dominance during the campaign periods: Prague (biomass and coal combustion), Barcelona (fuel oil combustion, secondary photochemical organics) and Athens (secondary photochemical organics). The on-going toxicological studies will clarify the health significance of these findings

Adsorption of marine phycotoxin okadaic acid on a covalent organic framework

Phycotoxins, compounds produced by some marine microalgal species, can reach high concentrations in the sea when a massive proliferation occurs, the so-called harmful algal bloom. These compounds are especially dangerous to human health when concentrated in the digestive glands of seafood. In order to generate an early warning system to alert for approaching toxic outbreaks, it is very important to improve monitoring methods of phycotoxins in aquatic ecosystems. Solid-phase adsorption toxin tracking devices reported thus far based on polymeric resins have not been able to provide an efficient harmful algal bloom prediction system due to their low adsorption capabilities. In this work, a water-stable covalent organic framework (COF) was evaluated as adsorbent for the hydrophobic toxin okadaic acid, one of the most relevant marine toxins and the parental compound of the most common group of toxins responsible for the diarrhetic shellfish poisoning. Adsorption kinetics of okadaic acid onto the COF in seawater showed that equilibrium concentration was reached in only 60 min, with a maximum experimental adsorption of 61 mg g1. Desorption of okadaic acid from the COF was successful with both 70% ethanol and acetonitrile as solvent, and the COF material could be reused with minor losses in adsorption capacity for three cycles. The results demonstrate that COF materials are promising candidates for solid-phase adsorption in water monitoring devices.This article is a result of the project Nanotechnology Based Functional Solutions (NORTE-01-0145-FEDER-000019), supported by Norte Portugal Regional Operational Programme (NORTE2020) under the PORTUGAL 2020 Partnership Agreement through the European Regional Development Fund (ERDF). This project has received funding from the European Union’s Seventh Framework Programme for research, technological development and demonstration under grant agreement no. 600375.info:eu-repo/semantics/publishedVersio

Bundling up carbon nanotubes through Wigner defects

We show, using ab initio total energy density functional theory, that the so-called Wigner defects, an interstitial carbon atom right besides a vacancy, which are present in irradiated graphite can also exist in bundles of carbon nanotubes. Due to the geometrical structure of a nanotube, however, this defect has a rather low formation energy, lower than the vacancy itself, suggesting that it may be one of the most important defects that are created after electron or ion irradiation. Moreover, they form a strong link between the nanotubes in bundles, increasing their shear modulus by a sizeable amount, clearly indicating its importance for the mechanical properties of nanotube bundles.Comment: 5 pages and 4 figure

Considerations for the design and conduct of human gut microbiota intervention studies relating to foods

With the growing appreciation for the influence of the intestinal microbiota on human health, there is increasing motivation to design and refine interventions to promote favorable shifts in the microbiota and their interactions with the host. Technological advances have improved our understanding and ability to measure this indigenous population and the impact of such interventions. However, the rapid growth and evolution of the field, as well as the diversity of methods used, parameters measured and populations studied, make it difficult to interpret the significance of the findings and translate their outcomes to the wider population. This can prevent comparisons across studies and hinder the drawing of appropriate conclusions. This review outlines considerations to facilitate the design, implementation and interpretation of human gut microbiota intervention studies relating to foods based upon our current understanding of the intestinal microbiota, its functionality and interactions with the human host. This includes parameters associated with study design, eligibility criteria, statistical considerations, characterization of products and the measurement of compliance. Methodologies and markers to assess compositional and functional changes in the microbiota, following interventions are discussed in addition to approaches to assess changes in microbiota–host interactions and host responses. Last, EU legislative aspects in relation to foods and health claims are presented. While it is appreciated that the field of gastrointestinal microbiology is rapidly evolving, such guidance will assist in the design and interpretation of human gut microbiota interventional studies relating to foods

Friend or foe? The current epidemiologic evidence on selenium and human cancer risk.

Scientific opinion on the relationship between selenium and the risk of cancer has undergone radical change over the years, with selenium first viewed as a possible carcinogen in the 1940s then as a possible cancer preventive agent in the 1960s-2000s. More recently, randomized controlled trials have found no effect on cancer risk but suggest possible low-dose dermatologic and endocrine toxicity, and animal studies indicate both carcinogenic and cancer-preventive effects. A growing body of evidence from human and laboratory studies indicates dramatically different biological effects of the various inorganic and organic chemical forms of selenium, which may explain apparent inconsistencies across studies. These chemical form-specific effects also have important implications for exposure and health risk assessment. Overall, available epidemiologic evidence suggests no cancer preventive effect of increased selenium intake in healthy individuals and possible increased risk of other diseases and disorders