Harnessing the climate commons: an agent-based modelling approach to making reducing emission from deforestation and degradation (REDD)+work

Humans have created a worldwide tragedy through free access to the global common atmosphere. The Conference of the Parties (COP) on climate change increased political commitment to reduce emission from deforestation and degradation and to enhance carbon stocks (REDD+). However, government sectors, political actors, business groups, civil societies, tree growers and other interest groups at different levels may support or reject REDD+. The paper used Arena-Actor-Institution concept to understand REDD+and provides agent-based modeling approach to harnessing its processes. The model explores: (a) how providers are likely to decrease or increase carbon stocks on their landscapes under ‘business as usual’ institutions; (b) how they are likely to negotiate with potential buyers with regards to the involvement of brokers (governments or nongovernmental organizations); and (c) how altruism and collaboration can affect the affectivity of REDD+. The model was developed as a spatially explicit model to consider the complexity of REDD+target landscapes. The simulation results are examined against the 3E+criteria, i.e. effectiveness in carbon emission reduction, cost efficiency and equity among involved stakeholders and co-benefit of other activities. This study took the Jambi landscape in Indonesia as a case. The results explain how REDD+agreement areas increase with higher carbon prices, e.g. US$25 or US$35. However, the simulation also shows that even with low carbon prices GHG emissions will decrease if the altruism degree and collective actions of the actors increases. The paper describes institutional arrangements which would help to harness the global commons of climate change.     

Leaching behavior of polychlorinated dibenzo-p-dioxins and furans from the fly ash and bottom ash of a municipal solid waste incinerator

The leaching behavior of dioxins from landfill containing bottom ash and fly ash from municipal solid waste incineration has been investigated by leaching tests with pure water, non-ionic surfactant solutions, ethanol solutions, or acetic acid solutions as elution solvents for a large-scale cylindrical column packed with ash. Larger amounts of dioxins were eluted from both bottom ash and fly ash with ethanol solution and acetic acid solution than with pure water. Large quantities of dioxins were leached from fly ash but not bottom ash by non-ionic surfactant solutions. The patterns of distribution of the dioxin congeners in the leachates were very similar to those in the bottom ash or fly ash from which they were derived.     

Climate change impacts on a large-scale erosion coast of Hai Hau district,Vietnam and the adaptation

Among the effects of global warming, sea level rise (SLR) and severe typhoons pose the greatest threat to the stability of human settlements along coastlines. Therefore, countermeasures must be developed to mitigate the influences of strong typhoons and persistent SLR for coastal protection. This study assesses climate change impacts on coastal erosion, especially in two projected SLR scenarios of RCP2.6 and RCP8.5. The results show that SLR and severe typhoons lead to the increase of coastal erosion, beach lowering and scour. Moreover, as in projected SLR scenarios, average waves in high tide can cause severe soil erosion at inner slopes and lead to dyke failure by 2060. The paper highlights the need for additional countermeasures to protect the coast of Hai Hau district against SLR and severe typhoons. Among the alternatives available for countering these threats, applying soil stabilization and soil improvement combined with geosynthetics are promising strategies for coastal structures. Hybrid structures can be used with earth reinforcement and soil improvement. Additionally, the paper emphasizes the importance of multiple protective adaptations, including geosynthetics and ecological engineering measures against climate change-induced severe erosion on the coast of Hai Hau district.     

Photodegradation of tetraphenyltin contained in polychlorinated biphenyl-based transformer oil simulants in alkaline 2-propanol solution

The photodegradation of tetraphenyltin (TePT) contained in polychlorinated biphenyl (PCB)-based transformer oil simulants by ultraviolet (UV) irradiation in alkaline 2-propanol solutions was examined. In the absence of PCBs, the TePT level fell to below 1% of the initial concentration within 30 min. In the absence of both PCBs and an alkali, the concentrations of tri-, di-, and monophenyltins initially increased to a few milligrams per liter, and then reduced to below the detection limits within 90 min. The addition of an alkali to the reaction solution slightly accelerated the photodecomposition of TePT. The decomposition of other phenyltins (PTs) was also accelerated. When PCBs with concentrations of approximately 80 times the initial TePT concentration were added, only a small fraction of the TePT decomposed within 100 min. Moreover, the levels of PTs did not change during irradiation. TePT and other PTs did decompose when the level of PCBs was reduced to the same concentration as that of TePT; however, the decomposition rates were slower than those in the absence of PCBs. In the actual treatment process, TePT and other PTs in PCB-based transformer oil are decomposed by catalytic reduction, which is used after UV irradiation. Therefore, in the actual treatment of PCB-based transformer oil wastes, pollution due to PTs can be prevented.     

Formation of dioxins from combustion of polyvinylidene chloride in a well-controlled incinerator

Polyvinylidene chloride (PVDC; polymer of 1,1-dichloroethylene) was combusted with paper in a well-controlled, small-scale incinerator at an average grate temperature of 700 °C, and then dioxins (PCDDs, PCDFs, and coplanar-PCBs) formed in the exhaust gases were analyzed by gas chromatography/mass spectrometry. PVDC lowered the combustion temperature due to its less flammable character. The amount of total dioxins (PCDDs + PCDFs + coplanar-PCBs) formed in the exhaust gas was 58.0 ng/g of a combustion sample and its toxicity equivalency quantity (TEQ) value was 0.64 ng-TEQ/g. The amount of PCDDs formed in the sample ranged from 2.33 ng/g (Cl₈-isomer) to 0.048 ng/g (Cl₁-isomer). The lower the number of chloride, the less production of PCDDs. On the other hand, there was no relation between the number of chloride and PCDF formation. The amount of PCDFs formed in the sample ranged from 8.02 ng/g (Cl₂-isomer) to 4.46 ng/g (Cl₈-isomer). A polyvinylchloride (PVC) sample produced 207 ng/g of total dioxins and a PVDC sample produced 57.4 ng/g of total dioxins when they were combusted under the same conditions. An approximately equal composition of dioxin isomers was formed from PVDC and PVC samples. Paper was found to contribute to PCDF formation when it was combusted with plastics.     

Removal of organic polyelectrolytes and their metal complexes by adsorption onto xonotlite

Natural organic polyelectrolytes (humic and fulvic acids) and their metal complexes were removed by adsorption onto xonotlite. The removal percentages of humic and fulvic acids by xonotlite were approximately 80% and 30%, respectively. Humic acid removal from solution by adsorption onto xonotlite took place more readily than fulvic acid removal. The molecular weight distributions of the humic substances remaining in solution after adsorption with the xonotlite were measured with size exclusion chromatography. A comparison of molecular weight distributions demonstrated conclusively that large molecular weight components were adsorbed preferentially, indicating that adsorption efficiency depends on the number of functional groups of humic substances. Furthermore, the surface topography of the adsorbent was observed before and after adsorption by scanning electron microscopy. The calculated heat of adsorption was of 330 kJ mol(-1) which was evaluated from the Clapeyron-Clausius equation. Therefore, the adsorption type can be considered chemical. Since xonotlite can be easily synthesized and obtained at low cost, the adsorption method of humic and fulvic acids is superior to their precipitation.     

Damage from the Great East Japan Earthquake and Tsunami - A quick report

The Tohoku region, Northeast Japan, was hit by a gigantic earthquake which occurred in the Pacific close to Tohoku, and subsequently by a giant tsunami. These hazards have caused huge damage on the eastern coast Japan. The earthquake’s magnitude was 9.0, the strongest ever recorded in Japan. The tsunami was also historical as its run-up height reached over 39 m. As of early May, 2011, over 24 thousand people were reported as dead or missing. Moreover, serious accidents at the Fukushima Nuclear Power Plants No.1 were caused by the effects of the tsunami. Therefore, the damage faced by Japanese people can be seen as a giant composite disaster. Although Japan, and the northeast of Japan in particular, has over a long time period increased its preparedness against earthquakes and tsunamis, huge damage still occurred. This paper considers why this tragedy occurred, and what unrecognized factors contributed to the high vulnerability of the area. To assist in answering such questions, this paper presents a timely report of the features of the earthquake and tsunami, the damage they caused, and the early efforts for recovery and reconstruction.