Doing the Right Thing: Relief Agencies, Moral Dilemmas and Moral Responsibility in Political Emergemcies and War

In recent years a new generation of relief workers and relief agencies has become embroiled in the heat of civil wars and political emergencies, and the humanitarian community has had to revisit its fundamental principles and address the ethics of what it does. This paper sets out to continue this important debate by emphasising that ethical analysis should always be an essential part of humanitarian practice. The paper seeks to recognise the difficult moral choices relief agencies are facing today and gives some practical guidelines to relief agency staff when confronting the ethics of a given situation. In particular, it hopes to introduce some ethical principles into the debate about humanitarianism and contribute to the moral vocabulary which is being developed to improve relief agencies' ethical analysis. The paper starts by looking at the essential characteristics of a moral dilemma, and the way in which other types of tough choice can masquerade as moral dilemmas. It then introduces some basic moral principles surrounding the key ethical notions of action, consequences and moral responsibility in an effort to show how relief agencies might begin to develop a process of ethical analysis in their work. Finally, it explores how relief agencies might develop a more intuitive form of ethical analysis based on an organisational conscience and moral role models.     

Secondary organic aerosol formation from ozone-initiated reactions with nicotine and secondhand tobacco smoke

We used controlled laboratory experiments to evaluate the aerosol-forming potential of ozone reactions with nicotine and secondhand smoke. Special attention was devoted to real-time monitoring of the particle size distribution and chemical composition of SOA as they are believed to be key factors determining the toxicity of SOA. The experimental approach was based on using a vacuum ultraviolet photon ionization time-of-flight aerosol mass spectrometer (VUV-AMS), a scanning mobility particle sizer (SMPS) and off-line thermal desorption coupled to mass spectrometry (TD-GC-MS) for gas-phase byproducts analysis. Results showed that exposure of SHS to ozone induced the formation of ultrafine particles (<100 nm) that contained high molecular weight nitrogenated species (m/z 400–500), which can be due to accretion/acid–base reactions and formation of oligomers. In addition, nicotine was found to contribute significantly (with yields 4–9%) to the formation of secondary organic aerosol through reaction with ozone. The main constituents of the resulting SOA were tentatively identified and a reaction mechanism was proposed to elucidate their formation. These findings identify a new component of thirdhand smoke that is associated with the formation of ultrafine particles (UFP) through oxidative aging of secondhand smoke. The significance of this chemistry for indoor exposure and health effects is highlighted.     

Ionic species associated with PM2.5 in the City of Guadalajara, México during 2007

Atmospheric aerosol particles were collected from January to December 2007 at two sites in the City of Guadalajara. The first site (Centro) is located in the downtown, which is characterized by high vehicular traffic, and the second site (Miravalle) is in the southern part of the city, characterized by emissions from high industrial and vehicular activity. Sulfates, nitrates, and ammonium were the most abundant ions at both sites. Similar concentrations of sulfates, nitrates, and ammonium were observed throughout the year at Centro while only sulfates and nitrates were similar at Miravalle. From the balance of anions and cations at the two sites, Centro was determined to have acidic particles, while at Miravalle, the particles were alkaline. Based on the analysis of the ammonium/sulfate molar ratios, it was determined that in Centro, there was not enough ammonium to neutralize the sulfate, while at Miravalle, ammonium practically neutralized all sulfate.     

Inputs of heavy metals due to agrochemical use in tobacco fields in Brazil’s Southern Region

Only a few studies have assessed the joint incorporation of heavy metals into agricultural systems based on the range of agrochemicals used on a specific agricultural crop. This study was conducted to assess the heavy metals input through application of the main agrochemicals used in Brazilian tobacco fields. A total of 56 samples of different batches of 5 fertilizers, 3 substrates, 8 insecticides, 3 fungicides, 2 herbicides, and 1 growth regulator commonly used in the cultivation of tobacco in Brazil’s Southern Region were collected from 3 warehouses located in the States of Rio Grande do Sul, Santa Catarina, and Paraná. The total As, Cd, Co, Cr, Cu, Hg, Fe, Mn, Ni, Pb, and Zn content of the samples was then determined and compared with the regulations of different countries and information found in the available literature. The fertilizers were identified as the primary source of heavy metals among the agrochemicals used. Application of pesticides directly to the shoots of tobacco plants contributed very little to the supply of heavy metals. The agrochemicals used in Brazilian tobacco fields provide lower inputs of the main heavy metals that are nonessential for plants than those registered in the international literature for the majority of crop fields in different regions of the world.     

Environmental water demand assessment under climate change conditions

Measures taken to cope with the possible effects of climate change on water resources management are key for the successful adaptation to such change. This work assesses the environmental water demand of the Karkheh river in the reach comprising Karkheh dam to the Hoor-al-Azim wetland, Iran, under climate change during the period 2010–2059. The assessment of the environmental demand applies (1) representative concentration pathways (RCPs) and (2) downscaling methods. The first phase of this work projects temperature and rainfall in the period 2010–2059 under three RCPs and with two downscaling methods. Thus, six climatic scenarios are generated. The results showed that temperature and rainfall average would increase in the range of 1.7–5.2 and 1.9–9.2%, respectively. Subsequently, flows corresponding to the six different climatic scenarios are simulated with the unit hydrographs and component flows from rainfall, evaporation, and stream flow data (IHACRES) rainfall-runoff model and are input to the Karkheh reservoir. The simulation results indicated increases of 0.9–7.7% in the average flow under the six simulation scenarios during the period of analysis. The second phase of this paper’s methodology determines the monthly minimum environmental water demands of the Karkheh river associated with the six simulation scenarios using a hydrological method. The determined environmental demands are compared with historical ones. The results show that the temporal variation of monthly environmental demand would change under climate change conditions. Furthermore, some climatic scenarios project environmental water demand larger than and some of them project less than the baseline one.     

Dry Deposition of Ammonia at Environmental Concentrations on Selected Plant Species

The deposition velocity of NH₃ on six plant species at environmental concentrations has been studied in a dynamic plant gas exchange reactor. The total resistance to the transport of NH₃ was studied. The aerodynamic resistance was determined directly by NH₃ gas absorption in aqueous solutions at environmental concentrations in a two-phase gradientless reactor modeling the transfer processes through the stomata in a leaf. The concentration of NH₃ in the gas phase ranged from 50 to 1000 ppb and the temperature varied from 25 to 30°C. The results for the deposition velocity for NH₃, during the day, varied from 0.3 to 1.3 cm/s. The deposition velocities at night were about one order of magnitude smaller. These results are compared with estimates from the Frdssling equation which consistently yields higher values of the same order of magnitude. To determine accurate atmospheric transport models or global budget models, a variable deposition velocity should be used to account for the diurnal and seasonal variations in the surface resistance.     

Distribution of bisphenol-A, triclosan and n-nonylphenol in human adipose tissue, liver and brain

In this study, an analytical method was optimized for the determination of bisphenol-A (BPA), triclosan (TCS) and 4-n-nonylphenol (4n-NP), environmental contaminants with potential endocrine disruptive activities, in human tissues. The method consisted of a liquid extraction step, derivatization with pentafluorobenzoylchloride followed by a clean-up on acidified silica and detection with gas chromatography coupled with mass spectrometry (GC-ECNI/MS). Recoveries ranged between 92% and 102% with a precision below 5%. Limits of quantification ranged between 0.3-0.4 ng g⁻¹, 0.045-0.06 ng g⁻¹ and 0.003-0.004 ng g⁻¹ for BPA, TCS and 4n-NP in different tissues, respectively. The method was applied for the determination of BPA, TCS and 4n-NP in paired adipose tissue, liver and brain samples from 11 individuals. BPA could be detected in almost all tissues, with the highest concentrations found in adipose tissue (mean 3.78 ng g⁻¹), followed by liver (1.48 ng g⁻¹) and brain (0.91 ng g⁻¹). TCS showed the highest concentrations in liver (3.14 ng g⁻¹), followed by adipose tissue (0.61 ng g⁻¹), while it could be detected in only one brain sample. Levels of 4n-NP were much lower, mostly undetected, and therefore 4n-NP is considered of minor importance for human exposure. Despite the measurable concentrations in adipose tissue, these compounds seem to have a low bioaccumulation potential. The reported concentrations of free BPA in the various tissues are slight disagreement with pharmacokinetic models in humans and rats and therefore the possibility of external contamination with BPA during sample collection/storage cannot be ruled out.