The destruction of mangroves

Coastal developments in Venezuela are leading to the rapid destruction of the mangrove forests. Population pressure leads to an overcrowding of public recreational beaches and the wealthy are increasingly seeking out previously deserted coasts. A rash of summer houses built on stilts over the shallow water is now extending around the mangrove areas, causing pollution, erosion and a progressive deterioration of the coastal environment.     

Robustness of pattern scaled climate change scenarios for adaptation decision support

Pattern scaling offers the promise of exploring spatial details of the climate system response to anthropogenic climate forcings without their full simulation by state-of-the-art Global Climate Models. The circumstances in which pattern scaling methods are capable of delivering on this promise are explored by quantifying its performance in an idealized setting. Given a large ensemble that is assumed to sample the full range of variability and provide quantitative decision-relevant information, the soundness of applying the pattern scaling methodology to generate decision relevant climate scenarios is explored. Pattern scaling is not expected to reproduce its target exactly, of course, and its generic limitations have been well documented since it was first proposed. In this work, using as a particular example the quantification of the risk of heat waves in Southern Europe, it is shown that the magnitude of the error in the pattern scaled estimates can be significant enough to disqualify the use of this approach in quantitative decision-support. This suggests that future application of pattern scaling in climate science should provide decision makers not just a restatement of the assumptions made, but also evidence that the methodology is adequate for purpose in practice for the case under consideration.     

Understanding carbon trading: Effects of delegating CO2 responsibility on organizations’ trading behaviour

The establishment of a carbon market assumes that there is an effective means of transforming price information into technical carbon reduction measures. However, empirical evidence reveals that the links between price information and carbon management strategies are far from obvious. To understand how delegating CO₂ responsibility affects CO₂ trading behaviour, this article proposes a neo-institutionalist approach to answering the question of why companies became sellers, buyers or a combination of both during phase I of the European Emissions Trading Scheme (EU ETS). Original data from a survey on companies that participated in this scheme were collected and analysed. It was assumed that the trading scheme offered two ways to delegate decisions regarding emissions trading: decoupling from technical knowledge and financialization (i.e. delegating to financial departments) or coupling using technicalization (i.e. delegating to manufacturing departments). The results support the hypothesis that a company that adopts a decoupling strategy is more likely to buy certificates to fulfil their emissions targets. Adopting a coupling strategy indicates that a company is more likely to become a seller, all else equal. Professional identity is the theoretical basis for this relationship. Delegating carbon management to different departments represents either a stronger coupling or a stronger decoupling from core technological processes.

Policy relevance

The transaction data from phase I of the EU ETS open new questions and possibilities regarding the reasons that drive selling and buying in companies. It is important to look not only at the traditional sources of transaction costs, but rather also at the reasons for these tensions. One important source is the professional education of the people in charge of the EU ETS. Tailored information that directly addresses the different professional backgrounds of managers working in both financial departments and more technical departments might help to lower these types of transaction costs. In today's context, important emitter countries, such as China and Korea, have launched their own emissions markets, copying many aspects of the EU ETS. For the positive development of these markets and as a way of establishing a global emissions market, these new schemes should learn from the EU ETS experience.     

On-site treatment of textile yarn dyeing effluents using an integrated biological–chemical oxidation process

This paper reports the results of the treatment of a yarn dyeing effluent using an integrated biological–chemical oxidation process. In particular, the biological unit was based on a sequencing batch biofilter granular sludge reactor (SBBGR), while the chemical treatment consisted of an ozonation step. Biological treatment alone was first performed as a reference for comparison. While biological treatment did not produce an effluent for direct discharge, the integrated process assured good treatment results, with satisfactory removal of chemical oxygen demand (up to 89.8 %), total nitrogen (up to 88.2 %), surfactants (up to 90.7 %) and colour (up to 99 %), with an ozone dose of 110 mg of ozone per litre of wastewater. Biomass characterization by fluorescence in situ hybridization has revealed that filamentous bacteria represented about 20 % of biomass (coherently with high sludge volume index values); thanks to its special design, SBBGR guaranteed, however, stable treatment performances and low effluent suspended solids concentrations, while conventional activated sludge systems suffer from sludge bulking and even treatment failure in such a condition. Furthermore, biomass characterization has evidenced the presence of a shortcut nitrification–denitrification process.     

Alteration kinetics of natural stones due to sodium sulfate crystallization: can reality match experimental simulations?

Salt decay is a very destructive mechanism that affects frequently the porous building materials of our architectural heritage. Sodium sulfate is one of the salts found in this context. It usually demonstrates high destructive power in salt crystallization tests because it can crystallize not only during evaporative processes but also when the temperature drops or when the salt solution comes into contact with pre-existing crystals. However, the use of extreme temperatures or successive wet/dry cycles also makes these tests unrepresentative of reality. To verify whether sodium sulfate can also be so destructive in field conditions, we have performed crystallization tests consisting of a single isothermal drying event. Three natural stones, relevant for the architectural heritage, were used for the purpose: Bentheimer sandstone, Ançã limestone, and a current Portuguese limestone of low porosity. The stones gave rise to distinct salt decay patterns: efflorescence, multilayer delamination and unilayer delamination, respectively. These morphological alterations were characterized at the micrometer scale by a new method based on what we have called the alteration kinetics curve. Such curve is calculated from topographic profiles obtained by a non-contact optical technique. The multilayer and unilayer delamination decay were also monitored by time-lapse photography. The work led us to conclude that sodium sulfate can indeed be also very destructive in field-representative conditions. Moreover, it showed that the optical method can be a valuable aid in the development of more realistic salt crystallization tests.     

Hydrogeochemistry and isotope techniques to determine water interactions in groundwater-dependent shallow lakes,Wet Pampa Plain,Argentina

This paper gives an account of the implementation of hydrochemical and isotopic techniques to identify and explain the processes that govern solute exchange in two groundwater-dependent shallow lakes in the Southeastern Pampa Plain of Argentina. Water samples (lakes, streams, spring water and groundwater) for hydrochemical and stable isotopic determination were collected and the main physical–chemical parameters were measured. The combination of stable isotope data with hydrogeochemical techniques was used for the identification of sources and preferential recharge areas to these aquatic ecosystems which allowed the explanation of the lake water origin. The hydrochemical processes which explain Los Padres Lake water chemistry are evaporation from groundwater, CO₂ input, calcite dissolution, Na⁺ release by Ca²⁺ and Mg²⁺ exchange, and sulfate reduction. The model that best aligns with La Brava Lake hydrochemical constraints includes: mixing, CO₂ and calcite dissolution, cationic exchange with Na⁺ release and Mg²⁺ adsorption, and to a lesser extent, Ca/Na exchange. This model suggests that the fractured aquifer contribution to this water body is greater than 50 %. An isotopic-specific fingerprint for each lake was identified, finding a higher evaporation rate for La Brava Lake compared to Los Padres Lake. Isotopic data demonstrate the importance of these shallow lakes as recharge areas to the regional aquifer, becoming areas of high groundwater vulnerability. The Tandilia Range System, considered in many hydrogeological studies as the impermeable bedrock of the Pampean aquifer, acts as a fissured aquifer in this area, contributing to low salinity waters and with a fingerprint similar to groundwater isotopic composition.     

Application of Laser‐Induced Breakdown Spectroscopy and Hyperspectral Images for Direct Evaluation of Chemical Elemental Profiles of Coprolites

This study demonstrates the application of laser‐induced breakdown spectroscopy (LIBS) and hyperspectral imaging to the investigation of coprolite and fossil samples. Solid samples from the Permian (seven coprolites and one fossil), Cretaceous (one coprolite) and Oligo‐Miocene (two coprolites) periods were directly analysed, and emission spectra from 186 to 1042 nm were obtained in several areas covering coprolite/fossil and rock material. Initial exploratory analyses were performed using principal component analysis with the data set normalised by the norm (Euclidean norm = 1). After identification and selection of emission lines of eleven elements (Al, Ca, Cr, Fe, K, Mg, Mn, Na, Ni, P and Si), the signals were normalised again by the relative intensity of the selected element. Phosphorus was identified mainly in the coprolites, while K and Na were primarily found in the rock material. In several cases, there was a positive correlation between Ca and P. A sample from the Oligo‐Miocene series was also analysed using inductively coupled plasma‐optical emission spectrometry (ICP‐OES) (rock and coprolites were analysed separately). Based on the quantitative results from ICP‐OES, it was confirmed that the tendency was the same as that observed with the results obtained from LIBS directly in the solid sample.