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Korea’s domestic emissions trading scheme commenced in January 2015. It targeted mainly industrial and power sectors, and compelled companies to transform how they manage energy efficiency and mitigate GHGs. This study sets out to explore how Korean companies evaluated their allocation position and engaged in emissions trading in the first compliance period, and to identify their views on trading barriers and policy expectations at the start of emissions trading. Questionnaire surveys and on-site interviews targeting Korean companies under the Korean emissions trading scheme were conducted at the start of operations (February to March 2015) and after the first compliance year (May 2016), respectively. Actual operation results are observed and compared with the survey findings. This study extrapolates implications for policy and presents suggestions for the government and the target companies in terms of how to improve the current emissions trading scheme in order to further stimulate emissions trading.
POLICY RELEVANCE
This study attempts to bridge the gap between companies and government policy in operating the domestic emission trading scheme in Korea. Empirical results, based on analysis of company-level data, reveal how businesses perceive K-ETS and how this relates to the operating results, which saw only limited trading of surplus emissions taking place in the early phase. Key barriers to active trading identified in the study include supply–demand imbalance, policy uncertainty and lack of preparedness of companies over carbon pricing. These barriers could be addressed by improved transparency of allowance allocation methods, possibly restricting carry-over of surplus allowances, ending policy uncertainty and providing more information to companies that can support companies’ policy understanding of the carbon pricing based on the market mechanism. Targeted companies should proactively participate in emissions trading in the early phase, in order to learn from it and prepare for the future introduction of auctioning. 相似文献
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Krystle Catalli Sang-Heon Shim Vitali B. Prakapenka Jiyong Zhao Wolfgang Sturhahn Paul Chow Yuming Xiao Haozhe Liu Hyunchae Cynn William J. Evans 《Earth and Planetary Science Letters》2010,289(1-2):68-75
Recent studies have indicated that a significant amount of iron in MgSiO3 perovskite (Pv) is Fe3+ (Fe3+/ΣFe = 10–60%) due to crystal chemistry effects at high pressure (P) and that Fe3+ is more likely than Fe2+ to undergo a high-spin (HS) to low-spin (LS) transition in Pv in the mantle. We have measured synchrotron Mössbauer spectroscopy (SMS), X-ray emission spectroscopy (XES), and X-ray diffraction (XRD) of Pv with all iron in Fe3+ in the laser-heated diamond-anvil cell to over 100 GPa. Fe3+ increases the anisotropy of the Pv unit cell, whereas Fe2+ decreases it. In Pv synthesized above 50 GPa, Fe3+ enters into both the dodecahedral (A) and octahedral (B) sites approximately equally, suggesting charge coupled substitution. Combining SMS and XES, we found that the LS population in the B site gradually increases with pressure up to 50–60 GPa where all Fe3+ in the B site becomes LS, while Fe3+ in the A site remains HS to at least 136 GPa. Fe3+ makes Pv more compressible than Mg-endmember below 50 GPa because of the gradual spin transition in the B site together with lattice compression. The completion of the spin transition at 50–60 GPa increases bulk modulus with no associated change in density. This elasticity change can be a useful seismic probe for investigating compositional heterogeneities associated with Fe3+. 相似文献
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Toxicity identification in metal plating effluent: implications in establishing effluent discharge limits using bioassays in Korea 总被引：1，自引：0，他引：1
Because of complexity and diversity of toxicants in effluent, chemical analysis alone gives very limited information on identifying toxic chemicals to test organisms. Toxicity identification evaluation (TIE) techniques have been widely used to identify toxicants in various samples including industrial wastewater as well as natural waters. In response to new regulation for effluent discharge in Korea, which will be effective from 2011, a necessity of studies emerges that investigates toxicity levels in industrial effluents. This work was a preliminary study examining toxicity levels in effluent from one metal plating factory using Daphnia magna (48 h immobility) and identifying toxicity-causing substances. Toxicity tests showed variability on different sampling occasions and the results of TIE methods indicated that both organic compounds and metals contributed to the observed toxicity in metal plating effluent. Further studies are necessary to help reduce effluent toxicity especially from direct dischargers, who will have to comply with the new regulation. 相似文献
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Distribution of persistent organic pollutants in bivalves from the northeast coast of China 总被引：1，自引：0，他引：1
To assess the levels of organochlorine compounds (OCs) in the Chinese coastal environment, monitoring study using bivalves was conducted in 2005. A total of 21 bivalve samples covering the northeastern coast of China were collected and analyzed. Organochlorine compounds were widely distributed in the Chinese coastal environment, with dichlorodiphenyltrichloroethane (DDT) contamination being particularly prevalent. The overall concentrations of PCBs, DDTs, HCHs, chlordane compounds (CHLs), dieldrin, and endosulfans in bivalves were in the ranges of 3.27-25.4, 54.8-2680, 1.42-25.5, n.d. (not detected)-2.28, n.d.-4.02, and n.d.-9.55 ng g(-1) on a dry weight basis, respectively. The concentrations of DDT and HCH compounds are relatively higher than those from the coastal areas of other Asian countries. DDT metabolites were predominant, suggesting that the degradation of DDT is in progress in the Chinese coastal environment. Still, however, DDTs of high concentration exceeding 1000 ng g(-1) were observed at 19% of the stations surveyed. Among HCH compounds, beta-HCH, which is an isomer with strong persistency, was observed predominantly. Compositions of DDT and HCH compounds imply that fresh input of the two compounds into the Chinese coasts is possibly low. 相似文献
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Floodplain effects on the transport of dissolved and colloidal trace elements in the East Pearl River,Mississippi 
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下载免费PDF全文 Substantial work suggests that floodplain wetlands could play a role in modifying fluvial fluxes of dissolved and colloidal trace elements. Yet, few studies have directly addressed this issue. We examined trace elements in the East Pearl River (Mississippi or Louisiana, USA), which is surrounded by wetlands that are temporally more or less connected to the river depending on river stage. Dissolved and colloidal trace element samples, along with ancillary data, including dissolved organic carbon and nutrients, were collected during eight surveys of this system at different flow stages from November 2007 to September 2008. Hydrology of the system is complex due to seasonal changes in water sources as well as potential inputs from the floodplain wetlands and the hyporheic zone. We therefore considered effects including nonconservative mixing of water sources, saltwater intrusion, and floodplain wetland flux requirements needed to support observed downstream concentration changes. During moderately high discharge, fluxes of many elements (e.g., Cd, Fe, Mn, and Zn) increased downstream by 20% or more, with inputs from the floodplain wetlands as the apparent source. At the highest discharge, however, wetland inputs to the river may have been rate‐limited (i.e., the wetland source was flushed faster than biogeochemical processes could regenerate dissolved or colloidal material). At low discharge, other effects, including saltwater intrusion and hyporheic zone interactions, are important. Both redox processes and organic ligands (or dissolved organic carbon), along with the supply of wetland inputs (or removal) relative to river fluxes, appear to be key factors determining floodplain wetland effects. While the behavior of some elements suggests they were dominantly affected by redox processes (Mn and V) or by organic complexation (dissolved Fe and light rare earths), other elements were affected by more than one process in ways that remain obscure (Cu). Overall our results are broadly consistent with previous field, laboratory, and modeling studies and suggest that a better understanding of the sources and transformations of Fe is a key area for future research. 相似文献
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Lee Jong-Seok Baek Ji-Yeon Jung Dawoon Shim Jae-Seol Lim Hak-Soo Jo Young-Heon 《Ocean Science Journal》2019,54(3):349-362
Ocean Science Journal - Observing coastal water depths is very important to understand physical processes of the coastal environment and manage coastal resources. In this study, a low-altitude... 相似文献
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The Raman spectra of bixbyite, Mn2O3, were measured up to 40 GPa at room temperature. Mn2O3 undergoes a phase transition from the C-type rare earth structure to the CaIrO3-type (post-perovskite) structure at 16–25 GPa. The transition pressure measured in Raman spectroscopy is significantly lower
than the pressure reported previously by an X-ray diffraction study. This could be due to the greater polarizability in the
CaIrO3-type structure, consistent with high-pressure observation on the CaIrO3 type in MgGeO3, although it is still possible that experimental differences may cause the discrepancy. Unlike the change at the perovskite
to CaIrO3-type transition, the spectroscopic Grüneisen parameter does not decrease at the C-type to CaIrO3-type transition. The spectroscopic Grüneisen parameter of the low-pressure phase (C type) is significantly lower than thermodynamic
Grüneisen parameter, suggesting significant magnetic contributions to the thermodynamic property of this material. Our Raman
measurements on CaIrO3-type Mn2O3 contribute to building systematic knowledge about this structure, which has emerged as one of the common structures found
in geophysically important materials. 相似文献
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Jee-Hyun Jung Hyun-Joong Kang Moonkoo Kim Un Hyuk Yim Joon Geon An Won Joon Shim Jung-Hwan Kwon 《Ocean Science Journal》2015,50(4):763-773
The performance of a lab-scale flow-through exposure system designed for the evaluation of ecotoxicity due to oil spills was evaluated. The system simulates a spill event using an oil-coated gravel column through which filtered seawater is passed and flows into an aquarium containing fish embryos of olive flounder (Paralichthys olivaceus) and spotted sea bass (Lateolabrax maculates). The dissolved concentrations of individual polycyclic aromatic hydrocarbons (PAHs) in the column effluent were monitored and compared with theoretical solubilities predicted by Raoult’s law. The effluent concentrations after 24 and 48 h were close to the theoretical predictions for the higher molecular weight PAHs, whereas the measured values for the lower molecular weight PAHs were lower than predicted. The ratios of the concentration of PAHs in flounder embryos to that in seawater were close to the lipid-water partition coefficients for the less hydrophobic PAHs, showing that equilibrium was attained between embryos and water. On the other hand, 48 h were insufficient to attain phase equilibrium for the more hydrophobic PAHs, indicating that the concentration in fish embryos may be lower than expected by equilibrium assumption. The results indicate that the equilibrium approach may be suitable for less hydrophobic PAHs, whereas it might overestimate the effects of more hydrophobic PAHs after oil spills because phase equilibrium in an oil-seawater-biota system is unlikely to be achieved. The ecotoxicological endpoints that were affected within a few days are likely to be influenced mainly by moderately hydrophobic components such as 3-ring PAHs. 相似文献