Magnetic activated carbon was prepared by adding a magnetic material to activated carbon that had been prepared from waste citrus peel in Jeju. The adsorption characteristics of an aqueous solution of the antibiotic trimethoprim (TMP) were investigated using the magnetic activated carbon, as an adsorbent, and response surface methodology (RSM). Batch experiments were carried out according to a four-factor Box-Behnken experimental design affecting TMP adsorption with their input parameters (TMP concentration: 50～150 mg/L; pH: 4～10; temperature: 293～323 K; adsorbent dose: 0.05～0.15 g). The significance of the independent variables and their interaction was assessed by ANOVA and t-test statistical techniques. Statistical results showed that TMP concentration was the most effective parameter, compared with others. The adsorption process can be well described by the pseudo-second-order kinetic model. The experimental isotherm data followed the Langmuir isotherm model. The maximum adsorption capacities of TMP, estimated with the Langmuir isotherm model were 115.9-130.5 mg/g at 293-323 K. Also, both the thermodynamic parameters, △H and △G, have both positive values, indicating that the adsorption of TMP by the magnetic activated carbon is an endothermic reaction and proceeds via an involuntary process.

Measurements on mass size distribution of roadside aerosols were obtained in downtown Jeju City from July 2018 to May 2020 using an 8-stage cascade impactor sampler and the compositions of aerosols were analyzed. The mass size distribution of total aerosols was bimodal with aerosols existing in both the fine and coarse modes. The mass size distributions of Na+, Mg2+, Ca2+, Cl-, NH4 + and SO4 2- were unimodal, whereas that of K+ was bimodal. For NO3 -, the size distribution in winter and spring was bimodal with the peaks in both fine and coarse modes, whereas for summer and autumn the distribution was unimodal with a peak in the coarse mode. NH4 + was found to co-exist with SO4 2- in the fine mode with an average molar ratio of [NH4 +]/[SO4 2-] equal to 2.05. Good correlation was observed between NO3 - and NH4 + in the fine mode particles in spring and winter. Based on the value of the marine enrichment factor for Cl-, Mg2+, K+, Ca2+ and SO4 2-, it may be inferred that a major part of the roadside aerosols in downtown Jeju City was largely contributed by terrigenous sources, although the influence of sea salt was normally present.

Jeju Special Self-Governing Province has implemented a self-governing environmental impact assessment system (Jeju-EIAS) in recognition of its autonomy. In this study, the institutional features of Jeju-EIAS were examined by analyzing the development projects whose consultation under Jeju-EIAS were completed from 1994 to 2019. The consultation procedure of Jeju-EIAS, such as the actual operation of Review Committee for Environmental Impact Assessment (EIA), the consent of the provincial council, and the regular follow-up activities for the implementation of EIA consultations, has been implemented differently from those of other metropolitan cities and provinces. Under Jeju-EIAS, types of development projects subject to consultation on EIA also take into account local conditions, and include the construction of aquarium basin and building. In addition, provisions concerning the scale of development projects is strengthened above the Korean Environmental Impact Assessment Act (EIA Act).

This study investigated the nitrate formation process, and mass closure of Particulate Matter (PM) were calculated over the urbanized area of Jeju Island. The data for eight water-soluble inorganic ions and nineteen elements in PM2.5 and PM10 were used. The results show that the nitrate concentration increased as excess ammonium increased in ammonium-rich samples. Furthermore, nitrate formation was not as important in ammonium-poor samples as it was in previous studies. According to the sum of the measured species, approximately 45~53% of gravimetric mass of PM remained unidentified. To calculate the mass closure for both PM2.5 and PM10, PM chemical components were categorized into secondary inorganic aerosol, crustal matter, sea salt, trace matter and unidentified matter. The results by the mass reconstruction of PM components show that the portion of unidentified matter was decreased from 52.7% to 44.0% in PM2.5 and from 45.1% to 29.1% in PM10, despite the exclusion of organic matter and elemental carbon.

To determine the size distributions of water-soluble inorganic ionic species (WSIS) in roadside aerosols, sampling experiments were carried out in the urban roadside area of Jeju City on August 2018 and January 2019 by using the eight-stage cascade impactor sampler. The mass of roadside aerosols were partitioned at 57% in fine fraction, 36-37% in coarse fraction, and 6-7% in giant fraction, regardless of summer and winter. The mass concentrations of WSIS except for Na+ and SO42- in roadside aerosols were higher in winter than in summer. The size distributions of Na+, Mg2+, Ca2+ and Cl- were characterized by bimodal types with coarse particle mode peaking around 3.3-4.7㎛ and 5.8-9.0㎛ . The size distributions of NO3 - and K+ shifted from a single fine mode peaking around 0.7-1.1㎛ in winter to bimodal and/or trimodal types with peaks around coarse mode in summer. SO4 2- and NH4 + showed a single fine mode peaking around 0.7-1.1㎛ . The MMAD of roadside aerosols was lower than that of Na+, Mg2+, Ca2+ and Cl-. Based on the marine enrichment factors and the ratio values of WSIS and the corresponding value for sea water, the composition of roadside aerosols in Jeju City may be practically affected by terrestrial sources rather than marine source.

This study observed particulate matter (PM2.5 and PM10) in the downtown area of Jeju City, South Korea, to understand the chemical composition of particulates based on an analysis of the water-soluble ionic species contained in the particles. The mass fraction of the ionic species in the sampled PM10 and PM2.5 was 44.3% and 42.2%, respectively. In contrast, in Daegu City and Suwon City, the mass fraction of the ionic species in PM2.5 was higher than that in PM10. The chloride depletion percentage of PM10 and PM2.5 in Jeju City was higher than 61% and 66%, respectively. The contribution of sea-salt to the mass of PM10 (5.9%) and PM2.5 (2.6%) in Jeju City was similar to that in several coastal regions of South Korea. The mass ratio of Cl- to Na+ in the downtown area of Jeju City was comparable to that in some coastal regions, such as the Gosan Area of Jeju Island, Deokjeok Island, and Taean City. The mass fraction of sea-salt in PM10 and PM2.5 was very low, and the concentration of sodium and chloride ions in PM10 was not correlated with those in PM2.5 (R2 < 0.2), suggesting that the effects of sea-salt on the formation of particulate matter in Jeju City might be insignificant. The relationship between NH4 + and several anions such as SO4 2-, NO3 -, and Cl-, as well as the relationship between the measurement and calculation of ammonium ion concentration, suggested that sea-salts may not react with H2SO4, and (NH4)2SO4 may be a major secondary inorganic aerosol component of PM2.5 and PM10 in Jeju City.

From November 2013 to December 2016, ambient fine particulate matter (PM2.5) was sampled in the downtown area of Jeju City, South Korea, which has seen rapid urbanization. The atmospheric concentrations of elements were measured in the PM2.5 samples. This study focused on Cd, Cr, Cu, Mn, Ni, Pb, As, Sb, Sn, V, and Zn. The concentrations of Al, Na, K, Fe, Ca, Mg, Sr, and La were also obtained for reference. The objectives of this study were to examine the contributions of these elements to PM2.5 concentrations in downtown Jeju City, and to investigate the inter-element relationships and the elemental sources by using enrichment factors and principal components analysis (PCA). A composition analysis showed that the 19 elements constituted 6.65 % of the PM2.5 mass, and Na, K, Al, Fe, Ca, Mg, and Zn constituted 98 % of the total ion mass. Seasonal trend analysis for the sampling period indicated that the concentrations of the elements increased from November to April. However, no substantial seasonal variations were found in the concentrations of the elements. The composition ratios of some elements (Cu/Zn, Cu/Cd, Cu/Pb, V/Ni, and V/La) were found to be out of range when compared to the literature from other urban areas. The ratios between the elements and the PCA results showed that local contaminant sources in Jeju City rarely influence the composition of PM2.5. This suggests that the major sources of PM2.5 in Jeju City may include long-range transport of fine particulate matter produced in other areas.

This study was carried out to elucidate the chemical compositions of water-soluble inorganic ions in PM10 and PM2.5 aerosols collected during summer and winter in downtown Jejusi city. The ratios of NO3 - to the total mass of ionic species in PM10 and PM2.5 aerosols largely increase in winter compared to summer, while SO4 2- ratios in both aerosols appear to follow the opposite trend. Moreover, concentrations of Na+, Mg2+, Ca2+ and Cl- in PM10 and PM2.5-10 aerosols are higher in winter than in summer. The nitrate concentrations in PM10 and PM2.5 aerosols increase with an identical increase in excess ammonium during winter, however, nitrate formation during summer is not important owing to ammonium-poor conditions.

Chemical properties of aerosols were investigated by analyzing the inorganic water-soluble content in PM2.5 collected in the downtown area of Jeju City in Jeju Island. Due to an increase in both the number of visiting tourists and the size of local population, the number of cars in this area is increasing, causing an increase in PM2.5. Eight PM2.5-bound major inorganic ions were analyzed during the summer and winter periods. The water-soluble inorganic component represents a significant fraction of PM2.5. In particular, secondary inorganic aerosols contribute 36.2% and 47.5% of PM2.5 mass in summer and winter, respectively. Nitrate concentrations increase for [NH4 +]/[SO4 2-]>1.5, and excess ammonium, which is necessary for ammonium nitrate formation, is linearly correlated with nitrate. These results are clearly observed during the winter because conditions are more conducive to the formation of ammonium nitrate. A significant negative correlation between Nitrogen Oxidation Ratio (NOR) and temperature was observed. The obtained results can be useful for a better understanding of the aerosol dynamics in the downtown area in Jeju City.

In this study, mass concentrations and chemical compositions of PM2.5, including water-soluble ions and elements were determined at the 1,100 m-highland of Mt. Hallasan in Jeju Island across four seasons from August 2013 to August 2014. The average mass concentration of PM2.5 was 12.5±8.41 /m3 with 45.8% of the contribution from eight water-soluble ionic species. Three ionic species (SO4 2-, NH4 +, and NO3 -) comprised 96.2% of the total concentration of ions contained in PM2.5 and were the dominant ions, accounting for 43.5% of the PM2.5 mass at Mt. Hallasan. On the basis of the mass concentration level, seasonal variation, enrichment factor, and relationship among elements, we can presume that Mg, K, Ca, Mn, Fe, Co, Sr, Ba, Nd, and Dy originated mainly from crust or soil and that V, Cr, Ni, Cu, Zn, As, Cd, and Pb were significantly enriched in PM2.5 owing to the effects of the anthropogenic emissions. These results and the local distribution of emission sources and topographic characteristics near this sampling site suggest that the compositions of PM2.5 collected at the 1100 m-highland of Mt. Hallasan were largely influenced by inflow from outside of Jeju Island.

The purpose of this study is to show the geographical distribution and the temporal variation of the emission amount of biogenic volatile organic compounds(BVOCs) emanated from forests at Jeju Island. The total emission amount of BVOCs calculated by using the CORINAIR Methodology is 3612 ton yr-1 at Jeju Island. More than half of BVOCs emissions is come from coniferous forest, and 45 per cent from broad leaved forest. The others is attributed to grassland. Of total emission of BVOCs, isoprene accounts for 28 per cent, monoterpene for 32 per cent, and other VOCs for about 40 percent, respectively. It can be shown that 3000~10000 kg yr-1 of BVOCs is emitted at the zone with dense forest from an altitude of 500 m to the top of Mt. Halla, and less than 1500 kg yr-1 at the zone an altitude of below 500 meters. The monoterpene emission is more than 1500 kg yr-1 due to the existence of a colony of Abies koreana at the place with more than 1500 meters and a community of Pinus thunbergii and Cryptomeria japonica at the elevation of 500~700 m. In the case of isoprene emission, there is 1500~3000 kg yr-1 at the zone of an elevation from 700 m to 1500 m due to dense broad leaved forest and very little of its emission at an elevation of more than 1500 meters because there is hardly broad leaved trees grown. In this study, emission of BVOCs according to the altitude above sea level is estimated under the situation of lack of the data for broad leaved tree. More detailed data and information for the distribution of broad leaved trees are needed in order to calculate more realistic BVOC emission.

This study was carried out to estimate the BVOCs emissions with the emission factors which reflected the native conditions of forests in Jeju Island. This study made effective use of the previous data for the weather data and the emission rate of each organic volatile component measured at 10 species of conifers and broad leaved trees. The CORINAIR method and the grid system of 1km×1km for whole area of Jeju Island were adopted in calculating the BVOCs emission emitted from forest. The vegetation information for Jeju Island was referred to GIS and a government report. By the results of BVOCs emission for Jeju Island, the 85% of monoterpene emission was emitted from conifers and the others was from broad leaved trees. Most of monoterpene emission was attributed to Pinus thunbergii and Cryptomeria japonica. The broad leaved trees greatly contributed to the isoprene emission and Quercus serrata played a dominant role in emission of isoprene. The total amount of BVOCs emission was estimated as 3612 ton yr-1 in Jeju Island. The 51.1% of total emission was contributed to conifers, the 44.9% to broad leaved trees, and the 4.0% to grassland. Of total emission of BVOCs, monoterpene accounted for 32.3%, isoprene for 28.0%, and OVOCs for 39.7%. The BVOCs emission estimated by this study was less than that estimated by other previous study. This means that it is important to survey the emission rate at native conditions and gather the detailed information for various species of vegetation on target region.

The number concentrations and the water soluble ionic concentrations of PM2.5 have measured at Gosan site in Jeju, Korea, from March 2010 to December 2010, to clarify their characteristics. PM2.5 number concentrations vary from 22.57 to 975.65 particles/㎝3 with an average value of 240.41 particles/㎝3, which have been recorded evidently high in spring season as compared with those in other season. And the concentrations in small size ranges are greatly higher than those in large size ranges, so the number concentration in the size range 0.25∼0.45 ㎛ has more than 94% of the total number concentration of PM2.5. The major ionic components in PM2.5 are SO4 2-, NH4 + and NO3 -, which are mainly originated from anthropogenic sources, on the other hand, the concentrations of Cl-, K+, Ca2+ and Mg2+ are recorded relatively lower levels. The concentrations of the major ionic components are very high in spring season, but the concentration levels of the other components are recorded significantly high in winter season. On the other hand, in summer season, the lowest concentration levels are observed for overall components as well as the sum of them. The concentration ratios of nss-SO4 2-/SO4 2- and nss-Ca2+/Ca2+ are 98.1% and 88.9%. And the concentration ratio of SO4 2-/NO3 -(3.64) is greatly higher than the value in urban area due to no large NOx emission sources in the measurement. In addition, the correlation and the factor analysis for the number and the ionic concentrations of PM2.5 are performed to identify their sources. From the Pearson correlation analysis and the factor analysis, it can be suggested that the smaller parts(<0.5 ㎛) of PM2.5 is contributed by anthropogenic sources, but the sources of the remaining larger parts of PM2.5 are not able to be specified sources in this study.

The number concentrations, the mass concentrations and the elemental concentrations of PM10 have measured at Gosan site in Jeju, Korea, from March 2010 to December 2010. And the correlation and the factor analysis for the number, the mass and the elemental concentrations of PM10 are performed to identify their relationships and sources. The average PM10 number concentration is observed 246 particles/㎝3(35.7∼1,017 particles/㎝3) and the average PM10 mass concentration is shown 50.1 ㎍/㎥(16.7∼441.4 ㎍/㎥) during this experimental period. The number concentrations are significantly decreased with increasing particle size, hence the concentrations for the smaller particles less than 2.5 ㎛(PM2.5) are contributed 99.6% to the total PM10 number concentrations. The highest concentration of the 20 elements in PM10 determined in this study is shown by S with a mean value of 1,497 ng/㎥ and the lowest concentration of them is found by Cd with a mean value of 0.57 ng/㎥. The elements in PM10 are evidently classified into two group based on their concentrations: In group 1, including S>Na> Al>Fe>Ca>Mg>K, the elemental mean concentrations are higher than several hundred ng/㎥, on the other hand, the concentrations are lower than several ten ng/㎥ in group 2, including Zn>Mn>Ni>Ti>Cr>Co>Cu>Mo>Sr>Ba>V >Cd. The size-separated number concentrations are shown positively correlated with the mass concentrations in overall size ranges, although their correlation coefficients, which are monotonously increased or decreased with size range, are not high. The concentrations of the elements in group 1 are shown highly correlated with the mass concentrations, but the concentrations in group 2 are shown hardly correlated with the mass concentrations. The elements originated from natural sources have been predominantly related to the mass concentrations while the elements from anthropogenic sources have mainly affected on the number concentrations of PM10.

Jeju Special Self-Governing Province has the natural assets resulting in UNESCO World Biosphere Reserve, World Heritage Listed and World Geopark Certification, so the principle of 'Conservation First Development Later' has been set up for the vision of environmental policy to preserve these assets. This case study has been carried out to investigate the realization of the principle of 'Conservation First Development Later' for the development projects performed environmental impact assessment from 1994 to 2012 in Jeju Province, using geographic information systems(GIS). The Jeju Province has its own ordinance to consult and operate an environmental impact assessment(EIA) system. In particular, the conservation area, such as, Absolute/Relative Conservation Area and Underground Water, Ecosystem and View Conservation Zone, has been assigned and managed specially to conserve the natural environment. The 179 projects has been performed EIA for last 18 years in Jeju Province, and then the Absolute Conservation Area has been included in 22 projects and the Relative Conservation Area has been included in 34 projects. However, the 2 projects only have included the Absolute Conservation Area for 7 years after 2005. This result suggests that the application of the principle for the Absolute Conservation Area is strengthened gradually. On the other hand, the 17 projects and the 24 projects have included the Underground Water Conservation Zone assigned grade 1 and 2, respectively, and the number has been increasing after 2004. The results show that it needs to strengthen the application of the principle for this Zone. And the Ecosystem Conservation Zone assigned grade 1 and 2 have been included in 1 project and 9 projects, respectively. It is considered from this result that the principle is realized successfully for the Ecosystem Conservation Zone. In addition, it could be known that the principle is applied well for the View Conservation Zone, in this study.

The aerosol number concentration have measured with an aerodynamic particle sizer spectrometer(APS) at Gosan in Jeju Island, which is known as background area in Korea, from March 2010 to February 2011. The obtained results of asian dust events and non-asian dust period have been compared. The results show that the entire averaged aerosol number concentration from APS measurement during asian dust events and non-asian dust period are about 341 particles/㎝3 and 240 particles/㎝3, respectively. During asian dust events, the number concentration in small size ranges(≤0.4 ㎛) are similar to non-asian dust period, however, those in large size ranges(≥0.7 ㎛) are very higher than non-asian dust period. The contributions of the size resolved number concentration(23 channel in 0.25∼10.0 ㎛) to total number concentration in that range are dramatically decreased with increased particle size. The contributions of smaller size ranges(≤0.4 ㎛) during asian dust events are very low compared with non-asian dust period, on the other hand, those of larger size ranges(≥0.4 ㎛) are higher than non-asian dust period. total aerosol number concentration are depended on the number concentration in range of smaller than 0.58 ㎛ during non-asian dust period and asian dust events. On the other hand, PM10 mass concentration has mainly affected with the number concentration in range of smaller than 1.0 ㎛ during non-asian dust period, however, during asian dust events, the mass concentration has mainly affected with the number concentration in range of 0.65∼3.0 ㎛.

The aerosol number concentration have measured with an aerodynamic particle sizer spectrometer(APS) at Gosan site, which is known as background area in Korea, from January to September 2011. The temporal variation and the size distribution of aerosol number concentration have been investigated. The entire averaged aerosol number concentration in the size range 0.25∼32.0 ㎛ is about 252 particles/㎝3. The number concentration in small size ranges(≤ 0.5 ㎛) are very higher than those in large size ranges, such as, the number concentration in range of larger than 6.5 ㎛ are almost zero particles/㎝3. The contributions of the number concentration to PM10 and/or PM2.5 are about 34%, 20.1% and 20.4% in the size range 0.25∼0.28 ㎛, 0.28∼0.30 ㎛ and 0.30∼0.35 ㎛, respectively, however, the contributions are below 1% in range of larger than 0.58 ㎛. The monthly variations in the number concentration in smaller size range(<1.0 ㎛) are evidently different from the variations in range of larger than 1.0 ㎛, but the variations are appeared similar patterns in smaller size range(<1.0 ㎛), also the variations in range of larger than 1.0 ㎛ are similar too. The diurnal variations in the number concentration for smaller particle(<1.0 ㎛) are not much, but the variations for larger particle are very evident. Size-fractioned aerosol number concentrations are dramatically decreased with increased particle size. The monthly differences in the size-fractioned number concentrations for smaller size range(<0.7 ㎛) are not observed, however, the remarkable monthly differences are observed for larger size than 0.7 ㎛.

The aerosol number concentration have measured with an aerodynamic particle sizer spectrometer(APS) at Gosan site in Jeju, Korea, from March 2010 to March 2011. And then the atmospheric aerosol number concentration, the temporal variation and the size distribution of aerosol number concentration have been investigated. The aerosol number concentration varies significantly from 748 particles/㎝3 to zero particles/㎝3. The average number concentration in small size ranges are very higher than those in large size ranges. The number concentrations in the size range 0.25∼0.28 ㎛, 0.40∼0.45 ㎛ and 2.0∼2.5 ㎛ are about 84 particles/㎝3, 2 particles/㎝3 and 0.4 particles/㎝3, respectively. The number concentrations in range of larger than 7.5 ㎛ are below 0.001 particles/㎝3. The seasonal variations in the number concentration for smaller particle(<1.0 ㎛) are not much, but the variations for larger particle are very evident. And strong amplitudes of diurnal variations of entire averaged aerosol number concentration are not observed. Size-fractioned aerosol number concentrations are dramatically decreased with increased particle size. The size-fractioned aerosol number concentrations in size range 0.8∼4.0 ㎛ during nighttime are evidently higher than during daytime, but similar levels are appeared in other size range. The seasonal differences in the size-fractioned number concentrations for smaller size range(<0.7 ㎛) are not observed, however, the remarkable seasonal differences are observed for larger size than 0.7 ㎛.

Contamination of butyltin compounds (BTs), namely tributyltin (TBT), dibutyltin (DBT) and monobutyltin (MBT), was evaluated in sediments collected inside Jeju Harbor in 2001. The concentrations of BTs in surface sediments were comparable to those in other sites of domestic and foreign countries. The high correlations between BTs in surface (r2 = 0.83～ 0.91) and core (r2 = 0.70～0.79) sediments and the significant correlations between BTs concentrations and the number of incoming and outgoing vessels indicated that DBT and MBT were mainly degraded from TBT based on antifouling paints of vessels etc. and other sources, such as DBT and MBT, could be ignored. The butyltin degradation indices ([DBT] + [MBT]/[TBT]) in surface sediments were in the range of 2.2～3.6 (mean 2.7), indicating that the parent compound, TBT, was inflowed into the surface sediments a long ago, degraded and deposited. The sedimentation age of BTs contaminated core sediments could not estimated because the content of 210Pb activity was nearly all the same and so the sedimentation rate could not obtained.

Ozone measurements made from 4 sites in Jeju Island have been analyzed, including those from two urban and two rural locales. The data were analyzed in terms of the seasonal and diurnal trends. It should be clear that the surface ozone levels in Jeju area would be relatively sensitive to the external ozone supply originated from the region of Northeast Asia. It seems to be that due to the reactions of ozone with NOx and CO, the average ozone level in Jeju City appears lower than that in Seogwipo City although Jeju City is the largest city in Jeju Island.