72 research outputs found

    The Great Acceleration of fragrances and PAHs archived in an ice core from Elbrus, Caucasus

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    The Great Acceleration of the anthropogenic impact on the Earth system is marked by the ubiquitous distribution of anthropogenic materials throughout the global environment, including technofossils, radionuclides and the exponential increases of methane and carbon dioxide concentrations. However, personal care products as direct tracers of human domestic habits are often overlooked. Here, we present the first research combining fragrances, as novel personal care products, and polycyclic aromatic hydrocarbons (PAHs) as combustion and industrial markers, across the onset of the Great Acceleration in the Elbrus, Caucasus, ice core. This archive extends from the 1930s to 2005, spanning the profound changes in the relationship between humans and the environment during the twentieth century. Concentrations of both fragrances and PAHs rose throughout the considered period, reflecting the development of the Anthropocene. However, within this rising trend, remarkable decreases of the tracers track the major socioeconomic crises that occurred in Eastern Europe during the second half of the twentieth century

    An extraction method for nitrogen isotope measurement of ammonium in a low-concentration environment

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    Ammonia (NH3) participates in the nucleation and growth of aerosols and thus plays a major role in atmospheric transparency, pollution, health, and climate-related issues. Understanding its emission sources through nitrogen stable isotopes is therefore a major focus of current work to mitigate the adverse effects of aerosol formation. Since ice cores can preserve the past chemical composition of the atmosphere for centuries, they are a top tool of choice for understanding past NH3 emissions through ammonium (NH4+), the form of NH3 archived in ice. However, the remote or high-altitude sites where glaciers and ice sheets are typically localized have relatively low fluxes of atmospheric NH4+ deposition, which makes ice core samples very sensitive to laboratory NH3 contamination. As a result, accurate techniques for identifying and tracking NH3 emissions through concentration and isotopic measurements are highly sought to constrain uncertainties in NH3 emission inventories and atmospheric reactivity unknowns. Here, we describe a solid-phase extraction method for NH4+ samples of low concentration that limits external contamination and produces precise isotopic results. By limiting NH3atm exposure with a scavenging fume hood and concentrating the targeted NH4+ through ion exchange resin, we successfully achieve isotopic analysis of 50 nmol NH4+ samples with a 0.6 ‰ standard deviation. This extraction method is applied to an alpine glacier ice core from Col du Dôme, Mont Blanc, where we successfully demonstrate the analytical approach through the analysis of two replicate 8 m water equivalent ice cores representing 4 years of accumulation with a reproducibility of ±2.1 ‰. Applying this methodology to other ice cores in alpine and polar environments will open new opportunities for understanding past changes in NH3 emissions and atmospheric chemistry.</p

    Pressure is not a state function for generic active fluids

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    Pressure is the mechanical force per unit area that a confined system exerts on its container. In thermal equilibrium, it depends only on bulk properties (density, temperature, etc.) through an equation of state. Here we show that in a wide class of active systems the pressure depends on the precise interactions between the active particles and the confining walls. In general, therefore, active fluids have no equation of state, their mechanical pressures exhibit anomalous properties that defy the familiar thermodynamic reasoning that holds in equilibrium. The pressure remains a function of state, however, in some specific and well-studied active models that tacitly restrict the character of the particle-wall and/or particle-particle interactions.Comment: 8 pages + 9 SI pages, Nature Physics (2015

    Пути дальнего переноса пыли на ледники Кавказа и химический состав снега на Западном плато Эльбруса

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    We present and discuss the chronology of dust deposition events documented by the shallow firn and ice cores extracted on the Western Plateau, Mt. Elbrus (5150 m a.s.l.) in 2009, 2012 and 2013. Snow and ice samples were analysed for major ions and minor element concentrations including heavy metals. Dust layers are formed on the surface of the glaciers as a result of atmospheric transport of mineral dust and aerosol particles to the Caucasus region. Satellite imagery (SEVIRI), trajectory models, and meteorological data were used for accurate dating of each the dust layers revealed in the ice cores. Then we tried to determine origins of the dust clouds and to investigate their transport pathways with high resolution (50–100 km). It was found that the desert dust is deposited on Caucasus glaciers 3–7 times in a year and it comes mainly from deserts of the Middle East and more rarely from the Northern Sahara desert. For the first time average annual dust flux (264 µg/cm2 per a year) and average mass concentration (1.7 mg/kg) over the period 2007–2013 were calculated for this region. The deposition of dust resulted in elevated concentrations consists of mostly ions, especially Ca2+, Mg2+, K+, and sulphates. Dust originated from various sources in the Middle East, including Mesopotamia, or similar dust clouds passing over the Middle East are characterised by high concentrations of nitrates and ammonia that may be related to atmospheric transport of ammonium from agricultural lands that may explain high concentrations of ammonium in the dust originating from this region. Mean values of crustal enrichment factors (EF) for the measured minor elements including heavy metals were calculated. We believe that high content of Cu, Zn and Cd can be a result of possible contribution from anthropogenic sources. Studies of the Caucasus ice cores may allow obtaining new independent data on the atmosphere circulation and high-altitude environment of this region.Исследованы образцы из снежных шурфов и керна из неглубоких скважин, пробуренных на Западном плато Эльбруса на высоте 5100 м в 2009, 2012 и 2013 гг. Образцы снега и льда проанализированы на содержание основных соединений и микроэлементов, включая тяжёлые металлы. В результате переноса минеральных частиц на ледники Кавказа в снежно-фирновой толще формируются отчётливо различимые горизонты загрязнения. Анализ космических снимков SEVIRI, полей оптической толщины атмосферы, траекторий движения воздушных масс и метеорологических данных позволил определить первичные источники минеральных частиц для переноса пыли с высокой точностью (50–100 км). Cоставлена хронология событий переноса пыли. Установлено, что такие явления происходят на Кавказе 3–7 раз в год. Пыль принесена на ледники Эльбруса с Ближнего Востока и из Северной Африки. Выполнено первое для Кавказа прямое определение количества твёрдого вещества, выпадающего из атмосферы на поверхность на больших высотах – 264 мкг/см2 в год. Химический анализ образцов снега из горизонтов загрязнения, образовавшихся в 2009 г., показал высокое содержание нитратов, аммония и сульфатов, что связано с поступлением пыли из сельскохозяйственных районов в Месопотамии. Обнаружено повышенное содержание Cu, Zn и Cd по сравнению с естественным фоном, что может указывать на повышенный региональный фон этих элементов в Северной Африке и на Ближнем Востоке, а также на вероятный вклад антропогенных аэрозолей.

    Source apportionment study on particulate air pollution in two high-altitude Bolivian cities: La Paz and El Alto

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    La Paz and El Alto are two fast-growing, high-altitude Bolivian cities forming the second-largest metropolitan area in the country. Located between 3200 and 4050 m a.s.l. (above sea level), these cities are home to a burgeoning population of approximately 1.8 million residents. The air quality in this conurbation is heavily influenced by urbanization; however, there are no comprehensive studies evaluating the sources of air pollution and their health impacts. Despite their proximity, the substantial variation in altitude, topography, and socioeconomic activities between La Paz and El Alto result in distinct sources, dynamics, and transport of particulate matter (PM). In this investigation, PM10 samples were collected at two urban background stations located in La Paz and El Alto between April 2016 and June 2017. The samples were later analyzed for a wide range of chemical species including numerous source tracers (OC, EC, water-soluble ions, sugar anhydrides, sugar alcohols, trace metals, and molecular organic species). The United States Environmental Protection Agency (U.S. EPA) Positive Matrix Factorization (PMF v.5.0) receptor model was employed for the source apportionment of PM10. This is one of the first source apportionment studies in South America that incorporates an extensive suite of organic markers, including levoglucosan, polycyclic aromatic hydrocarbons (PAHs), hopanes, and alkanes, alongside inorganic species. The multisite PMF resolved 11 main sources of PM. The largest annual contribution to PM10 came from the following two major sources: the ensemble of the four vehicular emissions sources (exhaust and non-exhaust), accountable for 35 % and 25 % of the measured PM in La Paz and El Alto, respectively; and dust, which contributed 20 % and 32 % to the total PM mass. Secondary aerosols accounted for 22 % (24 %) in La Paz (El Alto). Agricultural smoke resulting from biomass burning in the Bolivian lowlands and neighboring countries contributed to 9 % (8 %) of the total PM10 mass annually, increasing to 17 % (13 %) between August–October. Primary biogenic emissions were responsible for 13 % (7 %) of the measured PM10 mass. Additionally, a profile associated with open waste burning occurring from May to August was identified. Although this source contributed only to 2 % (5 %) of the total PM10 mass, it constitutes the second largest source of PAHs, which are compounds potentially hazardous to human health. Our analysis additionally resolved two different traffic-related factors, a lubricant source (not frequently identified), and a non-exhaust emissions source. Overall, this study demonstrates that PM10 concentrations in La Paz and El Alto region are predominantly influenced by a limited number of local sources. In conclusion, to improve air quality in both cities, efforts should primarily focus on addressing dust, traffic emissions, open waste burning, and biomass burning.</p

    Application of independent component analysis on raman images of a pharmaceutical drug product: pure spectra determination and spatial distribution of constituents

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    Independent component analysis (ICA) was used as a blind source separation method on a Raman image of a pharmaceutical tablet. Calculations were performed without a priori knowledge concerning the formulation. The aim was to extract the pure signals from the initial data set in order to examine the distribution of actives and major excipients within the tablet. As a method based on the decomposition of a matrix of mixtures of several components, the number of independent component to choose is a critical step of the analysis. The ICA_by_blocks method, based on the calculation of several models using an increasing number of independent components on initial matrix blocks, was used. The calculated ICA signals were compared with the pure spectra of the formulation compounds. High correlations between the two active principal ingredient spectra and their corresponding calculated signals were observed giving a good overview of the distributions of these compounds within the tablet. Information from the major excipients (lactose and avicel) was found in several independent components but the ICA approach provides high level of information concerning their distribution within the tablet. However, the results could vary considerably by changing the number of independent components or the preprocessing method. Indeed, it was shown that under-decomposition of the matrix could lead to better signal quality (compared to the pure spectra) but in that case the contributions due to minor components or effects were not correctly identified and extracted. On the contrary, over-decomposition of the original dataset could provide information about low concentration compounds at the expense of some loss of signal interpretability for the other compounds

    Amazonian biomass burning enhances tropical Andean glaciers melting

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    The melting of tropical glaciers provides water resources to millions of people, involving social, ecological and economic demands. At present, these water reservoirs are threatened by the accelerating rates of mass loss associated with modern climate changes related to greenhouse gas emissions and ultimately land use/cover change. Until now, the effects of land use/cover change on the tropical Andean glaciers of South America through biomass burning activities have not been investigated. In this study, we quantitatively examine the hypothesis that regional land use/cover change is a contributor to the observed glacier mass loss, taking into account the role of Amazonian biomass burning. We demonstrated here, for the first time, that for tropical Andean glaciers, a massive contribution of black carbon emitted from biomass burning in the Amazon Basin does exist. This is favorable due to its positioning with respect to Amazon Basin fire hot spots and the predominant wind direction during the transition from the dry to wet seasons (Aug-Sep-Oct), when most fire events occur. We investigated changes in Bolivian Zongo Glacier albedo due to impurities on snow, including black carbon surface deposition and its potential for increasing annual glacier melting. We showed that the magnitude of the impact of Amazonian biomass burning depends on the dust content in snow. When high concentration of dust is present (e.g. 100 ppm of dust), the dust absorbs most of the radiation that otherwise would be absorbed by the BC. Our estimations point to a melting factor of 3.3 +/- 0.8% for black carbon, and 5.0 +/- 1.0% for black carbon in the presence of low dust content (e.g. 10 ppm of dust). For the 2010 hydrological year, we reported an increase in runoff corresponding to 4.5% of the annual discharge during the seasonal peak fire season, which is consistent with our predictions
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