During the dismantling of nuclear facilities, a large quantity of radioactive concrete is generated and chelating agents are required for the decontamination process. However, disposing of environmentally persistent chelated wastes without eliminating the chelating agents might increase the rate of radionuclide migration. This paper reports a rapid and straightforward ion chromatography method for the quantification of citric acid (CA), a commonly used chelating agent. The findings demonstrate acceptable recovery yields, linearities, and reproducibilities of the simulated samples, confirming the validity of the proposed method. The selectivity of the proposed method was confirmed by effectively separating CA from gluconic acid, a common constituent in concretes. The limits of detection and quantification of the method were 0.679 and 2.059 mg·L−1, respectively, while the recovery yield, indicative of the consistency between theoretical and experimental concentrations, was 85%. The method was also employed for the quantification of CA in a real concrete sample. These results highlight the potential of this approach for CA detection in radioactive concrete waste, as well as in other types of nuclear wastes.

전 세계적으로 급격하게 성장하는 스마트농업의 중요 요소 중 하나인 자동 관개시스템은 토양수분 센서에서 계측한 데이터를 기반으로 관개시점과 관개량을 판단하기 때문에 토양수분 센서의 설치가 필수적이다. 하지만 국내의 경우 토양을 고려하지 않고 단순히 포장의 가운데에 센서를 설치하는 등 토양수분 센서의 설치 위치에 대한 기준이 마련되어 있지 않아 토양수분 계측 위치에 관한 기준 검토가 필요하다. 본 연구에서 통계학적 방법을 이용하여 토양수분의 대표 계측지점을 선정 연구를 수행하였다. 토양은 수직적 또는 수평적으로 불균일성을 갖기에 구명이 쉽지 않다. 따라서 포장 전체에 걸쳐 지속해서 편향이 발생하지만 특정 위치에서의 평균 토양수분이 시간에 따라 유지한다는 시간 안정성 개념을 기반으로, 평균 토양수분을 나타내는 대표지점 선정 연구를 수행하였다. 토양수분을 측정하기 위한 시스템을 제작하였고, TDR (Time Domain Reflectometry) 센서를 이용하여 총 30개 지점을 측정하였다. 2023년 5월부터 8월까지 측정한 날짜·지점별 데이터를 이용하여, 지점의 편향을 정량화하여 식별할 수 있는 MRD (Mean Relative Difference, 평균상대차이)와 측정의 정밀도를 나타내는 RD (Relative Difference, 상대차이)의 SDRD (Standard Deviation of Relative Difference, 표준편차)를 산출하고, MRD와 SDRD를 통합한 지표로써 RMSE (Root Mean Square Error, 평균제곱근오차) 를 구하여, 시간 안정성이 가장 높은 지점인 RMSE의 수치가 최소인 지점을 대표지점으로 선정하였다. 토양수분 센서로 측정한 데이터를 사용하여 지점별 RMSE를 산출하고 비교하여, 평균적인 토양수분을 나타내는 대표지점을 선정할 수 있음을 확인하였다.

A glassy carbon electrode modified with a composite consisting of electrodeposited chitosan and carboxylated multi-walled carbon nanotubes (e-CS/MWCNTs/GCE) was used as a working electrode for simultaneous determination of dopamine (DA), serotonin (5-HT) and melatonin (MT), which were related to circadian rhythms. The electrochemical characterizations of the working electrode were carried out via electrochemical impedance spectroscopy and chronocoulometry. It was found that electrochemical modification method, that was cyclic voltammetry, may can cause continuous CS polymerization on MWCNTs surface to form a dense membrane with more active sites on the electrode, and the electrochemically active surface area of e-CS/MWCNTs/GCE obtained was about 7 times that of GCE. The electrochemical behaviour of DA, 5-HT and MT on working electrode were carried out via differential pulse voltammetry and cyclic voltammetry. The results showed that e-CS/MWCNTs/GCE solved the problem that the bare electrode could not detect three substances simultaneously, and can catalyze oxidation potential difference as low as 0.17 V of two substances reaction at the same time, indicating very good electrocatalytic activity. By optimizing the detection conditions, the sensor showed a good linear response to DA, 5-HT and MT in the range of 20-1000 μmol/L, 9-1000 μmol/L and 20-1000 μmol/L, and the detection limits were 12 μmol/L, 10 μmol/L and 22 μmol/L (S/N = 3), respectively. In addition, the proposed sensor was successfully applied to the simultaneous detection of DA, 5-HT and MT in human saliva samples.

A simple and one-pot synthetic procedure using two different sources has been demonstrated to prepare heteroatoms doped reduced graphene oxide such as nitrogen-doped reduced graphene oxide (N-RGO) and sulfur-doped reduced graphene oxide (S-RGO). The N-RGO has been hydrothermally synthesized using urea as nitrogen precursor, wherein the S-RGO has been synthesized using dimethyl sulfoxide (DMSO) as sulfur precursor. The successful N-doping, S-doping and other physicochemical properties of N-RGO and S-RGO have been confirmed with different spectroscopic and electrochemical techniques. The results indicated that doping into the graphene structure exhibits a high conductivity and a better transfer of charge. Moreover, heteroatoms doped graphene (N-RGO and S-RGO) and graphene-related materials (RGO) have been applied for the individual detection of uric acid (UA). Interestingly, the N-RGO exhibited a lower limit of detection (LOD, S/N = 3) of 2.7 10– 5 M for UA (10–1000 μM) compared with undoped RGO and S-RGO. Furthermore, the simultaneous detection of UA in the presence of Xanthine (XA) has been demonstrated a wide linear range of detection for UA: 10–1000 μM, with unchanged concentration of XA to be 200 μM, and exhibited a low limit of detection of 8.7 10− 5 M ( S∕N = 3) for UA. This modified sensor based on N-RGO has revealed a high selectivity and reproducibility thanks to its large surface area, high catalytic properties, and chemical structure. Indeed, the practical applicability of the proposed sensor has been evaluated in milk samples even in the presence of high concentrations of UA with satisfactory results.

제충국(Tanacetum cineariaiaefolium), 데리스(Derris elliptica), 고삼(Sophora flavescens) 추출물은 다양한 해충을 방제하는데 사용되고 있다. 하지만, 국내에서 판매되고 있는 식물추춞물 자재는 유효성분의 표기가 없고, 살충농도와 살충시간에 대한 자료가 전무한 상황이다. 본 연구에서는 상 용화된 주요 식물추출물의 살충유효성분의 농도를 결정하고 복숭아혹진딧물에 대해 살충농도와 살충시간을 측정하였다. 식물추출물의 살충활성성분 인 pyrethrins, rotenone, matrine과 oxymatrine의 농도는 액체 크로마토그래피에서 표준물질을 활용하여 질량분석을 통해 측정하였다. 식물추출 물을 농도별로 희석하여 복숭아혹진딧물에 살포하여 살충력을 측정하였다. 표준화합물과 비교한 후 질량분석 및 결정했습니다. Myzus persicae에 대 한 lethal concentation과 lethal time을 조사했다. 살포 후 48시간 후 치사 농도(LC50)는 pyrethrins (20.4 ppm), roteone (34.1 ppm), matrine (29.6 ppm)였고, 100 ppm 살포한 LT50은 pyrethrins (13.4시간), rotenone (15.1시간), matrine (14.4시간)로 측정되었다. Kaplan-Meier 생존분 석 결과, 100 ppm에서 세 가지 식물 추출물의 LT50은 대조구인 화학 살충제인 Sulfoxaflor를 살포 처리구보다 유의하게 빨랐습니다. 본 결과는 복숭 아혹진딧물 방제를 위해 식물추출물의 제형화에 단일 또는 혼합 제제를 개발하는데 기준 살충농도와 살충시간을 제고하는데 의미가 있다.

Chelating agents in low and intermediate radioactive wastes can form complexes with radionuclides and increase the mobility of the radionuclides. According to the Korea Radioactive Waste Agency (Acceptance criteria for low and intermediate radioactive waste, WAC-SIL-2022-1), if the amount of residual chelating agents in the waste are greater than 0.1%, the chemical names and residual amounts should be specified; if greater than 1%, the waste must be solidified and contain no more than 8%. The existing method for analyzing chelates in radioactive waste was based on UV–Visible spectrophotometry (UV-Vis), but the new method is based on liquid chromatography/mass spectrometry (LC-MS). The analysis was performed in aqueous solution before applying to real samples. Since the real sample may contain several heavy metals, it is expected that the chelates will exist as complexes. Therefore, 1.0×10-4 mol L-1 of EDTA (Ethylenediaminetetraacetic acid), DTPA (Diethylenetriaminepentaacetic acid), NTA (Nitrilotriacetic acid), and excess metals in aqueous solution were analyzed using HPLC using RP (Reverse Phase) column and HILIC (Hydrophilic interaction) column. When the RP column was used, each substance eluted without separation at the beginning of the analysis. However, when analyzed using a HILIC column, the peaks of each substance were separated. LC-MS measurements using HILIC conditions resulted in separations with better sensitivity.

This study demonstrated a rapid and simple method for the determination of seven anions including halides and oxyhalides from the KURT underground water sample by capillary electrophoresis with UV detection. In nuclear waste disposal, some anions such as iodine, selenium, and technetium have been of great concern due to its high mobility and toxicity with a long half-life. It has been needed for a reliable analysis of anionic speciation because the high mobility of anions is easily affected by environmental conditions especially pH and salinity of underground water. Here this project is to develop a fast separation of seven anions including iodide, iodate, and selenite using capillary electrophoresis. The electroosmotic flow (EOF) was suppressed using a poly (ethyleneglycol) -coated capillary (DB-WAX capillary). As a result, anions migrated depending on their mobility under a reverse polarity condition (-15 kV) and the analysis time was within 15 min. UV detection was used at 200 nm. The RSDs for migration time were between 0.7% and 1.3% except for selenite of 5.1%. The RSDs for peak area were obtained between 2.9% and 7.4%. The calibration curves were linear from 10 to 200 mg/L with correlation coefficients greater than 0.9952. The LODs were 7.3, 10.9, 11.3, 12.9, 13.0, 13.9, and 17.4 mg/L for iodide, nitrate, bromide, selenite, bromate, tungstate and iodate. The KURT underground water sample spiked with seven anions at 50 mg/L were analyzed. The recoveries of spiked KURT sample ranged from 93.4% to 99.3%. The proposed method was successfully applied to determine seven anions in underground water sample.

Radiation from spent nuclear fuel (SNF) is one of key factors affecting the dissolution process of SNF and the source term from repository. The dissolution rate of uranium dioxide (UO2) matrix of SNF is expected to control the release of radionuclides from SNF in contact with water under geological disposal conditions. Based on the oxidative dissolution mechanism, the solubility of UO2 can increase significantly if the reducing environment near the fuel surface is altered by water radiolysis caused by radiation from SNF. Therefore, the analysis of water radiolysis products such as radicals (·OH, ·OH2, eaq, ·H) and molecules (H3O+, H2, H2O2) is perquisite for studies on the rate of such dissolution process to determine oxidation/dissolution mechanism and related rate constants. In this study we examined the two-known spectroscopic methods developed for H2O2 determination; one is the luminol-based chemiluminescence (luminol-CL) method and the other is the spectrophotometry using ferrous oxidation-xylenol orange complexation (FOX). Their applicability for quantitative analysis of H2O2 in potential aqueous samples from SNF dissolution studies was evaluated in terms of the analytical dynamic range (ADR), the limit of detection (LOD) and the interfering effects of various metal ions possibly present in real samples. The luminol-CL method exploits the chemiluminescence reaction caused by luminol; when in the presence of a metallic catalyst (e.g., Cu2+, Co2+), luminol emits a blue light (425 nm) at pH 10- 11 in response to oxidizing agents such as hydrogen peroxide. Although a flow-through reaction system is routinely employed to enhance the analytical sensitivity we achieved the ADR up to ~200 μM and LOD < 1 μM by a batch-wise CL detection using conventional cuvette cells and an intensified charge-coupled device (ICCD). Interestingly, it turned out that the interfering effects of other metal ions (e.g., UO2 2+, U4+, Fe2+ and Fe3+) is minimal, which should be advantageous for the luminol-CL method to be employed for samples potentially containing other metal ions. On the other hand, the FOX method spectrophotometrically analyzes H2O2 based on the difference in color (or absorption spectra) of Fe-xylenol orange (XO) complexes. Initially, the Fe2+-XO complex was provided in working solutions at pH 3, which was subsequently mixed with samples having H2O2 and allowed for quantitative oxidation of Fe2+ to Fe3+. Typically, by monitoring the absorbance of Fe3+-XO complex at 560-580 nm (λmax) the ADR up to ~100 μM and LOD ~1.6 μM were achieved. However, it is found that interfering effects from M3+ and M4+ ions are significant; these interfering metal ions can form XO complexes so as to directly contribute the measured absorbance. In contrast, the influence from M2+ ions was found to be negligible. To summarize we conclude that both methods can be applied for H2O2 determination for aqueous samples taken from SNF dissolution tests. However, prior to applying the FOX method the metal ion composition in those samples should be thoroughly identified not to overestimate the H2O2 concentration of samples. More details of underlying chemical reactions in both methods will be discussed in the presentation.

In the high-level waste disposal systems, colloids generated through the chemical erosion of bentonite buffers can serve as critical mediators for the transport of radionuclides from the disposal environment to the biosphere. The stability of these colloids is influenced by the chemical composition of the groundwater. According to DLVO theory, the Critical Coagulation Concentration (CCC) is the ionic strength at which the total repulsive force between colloids is either less than or equal to the total attractive force. At ionic strengths lower than the CCC, electrostatic double-layer repulsion outweighs van der Waals attraction, forming a repulsive barrier between particles. Conversely, at ionic strengths higher than the CCC, attractive forces dominate, leading to particle aggregation. To investigate the CCC of bentonite colloids, this study focused on Ca-type WRK bentonite. Colloids separated from a ten g/L bentonite suspension underwent centrifugation (1,200 g for 30 minutes) and dialysis (3,500 MWCO) to produce colloid samples. After adjusting the ionic strength from 0.1 mM to 10 mM, the particle size distribution was monitored as a function of aggregation time for approximately 20 days. Rate constants, calculated based on variations in ionic strength, were used to interpret the observed results. The experimental outcomes revealed that the CCC value for WRK bentonite colloids was an order of magnitude lower with CaCl2 than with NaCl. This suggests that Ca ions have a more significant impact on colloid stability, which has implications for the longterm safety of high-level waste disposal systems.

The demand for high-strength steel is rising due to its economic efficiency. Low-cycle fatigue (LCF) tests have been conducted to investigate the nonlinear behaviors of high-strength steel. Accurate material models must be used to obtain reliable results on seismic performance evaluation using numerical analyses. This study uses the combined hardening model to simulate the LCF behavior of high-strength steel. However, it is challenging and complex to determine material model parameters for specific high-strength steel because a highly nonlinear equation is used in the model, and several parameters need to be resolved. This study used the particle swarm algorithm (PSO) to determine the model parameters based on the LCF test data of HSA 650 steel. It is shown that the model with parameter values selected from the PSO accurately simulates the measured LCF curves.

지각판의 움직임은 오일러 극(Euler pole)을 중심으로 하는 회전운동으로 나타낼 수 있다. 우리는 먼저 지역적 지각판의 속도자료로부터 해당 판운동의 오일러 벡터를 근사적으로 결정하는 알고리즘을 다음과 같이 개발하였다; 1) 관측된 판속도자료로부터 평균 가상 오일러 극을 먼저 구하고, 2) 평균가상극과 관측지역의 중심을 통과하는 대원 위의 점들을 각각 극으로 설정하여, 3) 얻어지는 각 임시적 가상 모델의 판운동속도와 관측속도와의 차이의 제곱들의 합을 반복하여 구한 다음, 그 값이 최소가 되도록 보간법(interpolation)으로써 오일러 벡터를 결정함. 그런데 최근 우리는 이 와 근본적 개념은 같으나(최소제곱법), 제곱오차의 합의 편미분계수가 0이 되는 조건으로부터 곧바로 오일러 벡터를 결 정하는 알고리즘을 추가적으로 개발하였으며, 이 개선된 방법으로 판운동의 오일러 벡터를 보다 더 정확하게 산출하게 되었다. 한편 이 두 가지 방법을 최근 수년간의 한반도의 GPS 지각속도자료에 각각 적용하여 한반도 지각판의 오일러 벡터를 구하였으며, 얻어진 두 결과를 비교하였다.

This study was aimed to determine the changes in CO2 concentration according to the temperatures of daytime and nighttime in the CO2 supplemental greenhouse, and to compare calculated supplementary CO2 concentration during winter and spring cultivation seasons. CO2 concentrations in experimental greenhouses were analyzed by selecting representative days with different average temperatures due to differences in integrated solar radiation at the growth stage of leaf area index (LAI) 2.0 during the winter season of 2022 and 2023 years. The CO2 concentration was 459, 299, 275, and 239 μmol·mol-1, respectively at 1, 2, 3, and 4 p.m. after the CO2 supplementary time (10:00-13:00) under the higher temperature (HT, > 18°C daytime temp. avg. 31.7, 26.8, 23.8, and 22.4°C, respectively), while it was 500, 368, 366, 364 μmol·mol-1, respectively under the lower temperature (LT, < 18°C daytime temp. avg. 22.0, 18.9, 15.0, and 13.7°C, respectively), indicating the CO2 reduction was significantly higher in the HT than that of LT. During the nighttime, the concentration of CO2 gradually increased from 6 p.m. (346 μmol·mol-1) to 3 a.m. (454 μmol·mol-1) in the HT with a rate of 11 μmol·mol-1 per hour (240 tomatoes, leaf area 330m2), while the increase was very lesser under the LT. During the spring season, the CO2 concentration measured just before the start of CO2 fertilization (7:30 a.m.) in the CO2 enrichment greenhouse was 3-4 times higher in the HT (>15°C nighttime temperature avg.) than that of LT (< 15°C nighttime temperature avg.), and the calculated amount of CO2 fertilization on the day was also lower in HT. All the integrated results indicate that CO2 concentrations during the nighttime varies depending on the temperature, and the increased CO2 is a major source of CO2 for photosynthesis after sunrise, and it is necessary to develop a model formula for CO2 supplement considering the nighttime CO2 concentration.

본 연구에서는 기존 식품첨가물 분석법에서 합으로써 분 석되는 락색소를 laccaic acid A, B, C, E 4가지 성분으로 분류하고 개별적으로 정량 할 수 있는 분석법을 확립하였 다. Natural red 25를 사용하여 구조적으로 비슷한 laccaic acid A와 B를 1차적으로 분취한 후 2차로 A와 B를 분리 했다. 같은 방식으로 C와 D를 1차, 2차에 걸쳐 각각의 개 별 표준품으로 사용하였다. 락색소 불검출 시료 3가지 시료 (햄, 토마토 주스, 고추장)를 확보하여 0.05-107.2 μg/mL 범 위에서 결정계수(r2) 0.995 이상의 직선성을 확인하였다. 3 가지 시료에서 정밀도와 정확성을 측정한 결과, 일내 정 밀도는 0.2-12.3%, 정확도는 90.6-112.7% 범위 내에서 확인 되었으며 일간 정밀도는 0.3-13.3%, 정확도는 90.3-113.0% 범위내로 확인 되었다. 락색소를 사용하는 식품과 사용 금 지 식품에 대해 회수율을 측정한 결과, 사용 가능 식품에서 는 91.6-114.9% 범위의 회수율을 보였으며, 사용 불가 식품 의 경우 92.5-113.5% 범위의 회수율을 보였다. 락색소의 검 출 한계는 3가지 시료에서 검출한계 0.01-0.15 μg/mL, 정량 한계 0.02-0.47 μg/mL로 확인되었다. 락색소의 4가지 성분중 laccaic acid A와 C에 대한 측정 불확도를 산출한 결과, laccaic acid A의 측정 불확도는 13.65±0.39 mg/kg(신뢰수준 95%, K=2), laccaic acid C의 측정 불확도는 4.19±0.39 mg/kg(신뢰 수준 95%, K=2)로 비교적 낮은 측정불확도 값을 산출하 였다. 따라서 본 연구에서는 식품 중 락색소의 개별 분석 과 정성 및 정량분석을 위해 유효성이 검증된 분석법을 확립으로 식품 중 잔류물질 기준규격 설정 및 관리에 참 고 자료가 될 수 있고, 향후 매트릭스 효과에 따른 laccaic acid 개별 분석과 개별 활성 및 독성시험 연구의 근거 지 표가 될 수 있다고 판단된다.

본 연구는 국내 유통 조미건어포 27건 중 프로피온산, 안 식향산, 소브산 함량을 분석하였다. 식품의약품안전처 식 품공전의 분석 방법으로 GC-FID를 이용하여 프로피온산 을 분석하였고 HPLC-DAD를 이용하여 안식향산과 소브 산을 분석하였다. 그 결과 총 27건 중 프로피온산은 16건 (검출률 59%), 안식향산은 불검출, 소브산은 7건(검출률 26%)이 검출되었다. 조미건어포에서 프로피온산은 ND- 125.10 mg/kg의 농도로 검출이 되었으며 이는 미생물 최 소저해농도 이하의 수치로 보존 효과를 나타낼 수 없는 농도로 보여 의도적으로 첨가되지는 않았을 것으로 사료 된다. 또한, 소브산의 경우 소르빈산 칼륨이 표기된 시료 에서만 검출되었으며 표기된 시료 8건 중 7건에서만 검출 이 되었다. 소브산 검출 시료의 경우 658.18 mg/kg의 농도 까지 검출이 되었으며, 이는 그 사용 기준에 적합한 수치 였다. 본 연구는 향후 조미건어포에 대한 안전 관리를 위 한 기초자료로 사용될 수 있을 것으로 사료된다.

본 연구는 패류 독소 중 기억상실성 독성을 유발하는 domoic acid의 분석법 개선, 검증 및 분석적용성을 살펴보 았다. SAX 카트리지 정제, 검체 및 추출용매 양의 변경 과 더불어 이동상을 용매구매 조건으로 변경시킨 분석법 은 지중해담치, 홍게 그리고 멸치의 세 가지 매트릭스를 대상으로 세 농도에 대하여 식품공전법과 비교하여 유효 성을 검증하였다. 그 결과 변경된 분석법은 LOD 0.02-0.03 mg/kg, LOQ 0.05-0.09 mg/kg, 일내 및 일간 정확도 86.2- 100.4%와 일내 및 일간 정밀도 0.2-4.0%로 CODEX가이 드라인을 만족하는 우수한 분석능을 나타내었다. 특히 변 경된 시험법에서는 domoic acid와 유사한 머무름 시간을 갖는 방해물질이 검출되지 않아 위양성 결과를 방지할 수 있을 것으로 생각된다. 더 나아가 본 분석법이 국내 유통 중인 수산물을 대상으로 적용될 수 있는지 확인하고자 식 품공전의 기억상실성 패독 분석법과 함께 수산물에 적용 하여 분석하였다. 그 결과 5종의 수산물 87건 중 공전시 험법으로 분석했을 때 domoic acid가 검출된 시료는 없었 으나 변경된 분석법을 통하여 멸치 1건에 대하여 0.14 mg/ kg의 domoic acid이 미량 검출되었다. 따라서 본 연구에 서 확립된 분석법은 수산물 중 domoic acid 분석에 활용 이 가능할 것으로 보인다.

Botanical extracts are employed in management of aphids. Extracts from Tanacetum cineariaiaefolium, Derris elliptica, and Sophora flavescens are widely used to control various insects. In this study, we determined concentrations of active insecticidal compounds (Ais) in commercial botanical extracts of these plants, and we investigated the time and concentration for lethal results with the green peach aphid, Myzus persicae. The concentrations of Ais, pyrethrins from T. cineariaiaefolium, rotenone from D. elliptica, and matrine and oxymatrine from S. flavescens, were determined after their fractionation by liquid chromatography followed by mass analysis and comparison with standard compounds. The extracts were tested for lethality in a bioassay with green peach aphids. Sprays at defined doses were applied to tobacco leaves infested with aphid nymphs. The lethal concentrations (LC50) were 20.4 ppm for pyrethrins, 34.1 ppm for rotenone, and 29.6 ppm for matrine at 48 h after treatments. At 100 ppm application levels, the lethal time LT50 was 13.4 h for pyrethrin, 15.1 h for rotenone, and 14.4 h for matrine. Kaplan - Meier analysis indicated the lethal times for the three botanical extracts at 100 ppm were significantly faster than application of a chemical insecticide, Sulfoxaflor, applied at the recommended level. These results provide baselines to develop and formulate single or mixed preparations containing botanical extracts to control green peach aphids on commercial crops.

The honey bee, Apis mellifera, has a defense system, including detoxification, antioxidation, and immunity pathways, against external stimulation such as chemicals, stress, and pathogens. However, pesticides, particularly neonicotinoids and butenolids, have been recently reported to alter physiological changes in honey bee. In this study, we investigated the expression levels of eight genes categorized into detoxification (CYPQ3), antioxidation (CAT and SOD2), and immune system (Abaecin, Apidaecin, Defensin1, Defensin2, and Hymenoptaecin), in five tissues (Head, Thorax, Gut, Fat body, and Carcass) of honey bee treated with three pesticides (Acetamiprid, Imidacloprid, and Flupyradifurone) using quantitative real-time PCR. Gene expression patterns was varied depending on the type of pesticides and tissues. However, among eight genes, the expression levels of CYPQ3 was notably induced, but those of AMPs were generally reduced by all pesticides tested in this study in five tissues. These suggest that CYPQ3-mediated detoxification pathway is induced, but AMP-mediated immune system might be disrupted when honey bee is exposed to neonicotinoids and butenolid.

본 연구에서는 영종도에 위치한 인천과학고등학교 주변에 서식하는 개미와 개미집 근권토양을 두 차례에 걸쳐 채취한 것을 활용하여 토양미생물 순수분리 및 동정을 진행하였다. 채취된 개미의 더듬이의 모양, 털의 위치 및 분포 등의 형태학적 동정 및 DNA extraction을 통한 분자생물학적 동정을 통하여 채취한 개미를 Camponotus japonicus으로 결론하였다. 토양미생물을 연속희석법을 이용하여 확인한 결과 채취한 개미집 세 곳에서 각각 12, 18, 10개의 종이 동정되었다. 개미집 근권토양의 비옥도가 상대적으로 높다는 선행연구를 바탕 으로 ‘분리한 토양미생물이 다양한 유기물 분해 효소활성을 보일 것’이라는 가설을 세웠고, 이를 확인하기 위해 분별배지를 제작하여 디스크 확산법을 진행하였다. 실험 결과 개미집 근권 토양에서 분리된 균주가 일반 토양에 서 분리된 균주에 비해 높은 효소활성을 보임을 확인하였으며 개미집 근권 토양 미생물의 불용성인산 가용화능 이 우수함을 확인하였다. 이후 위 실험들을 바탕으로 개미집 근권 토양 미생물이 식물 생장을 촉진시켜 미생물을 접종한 토양에서의 식물의 건조 질량이 증가하였음을 확인하였다.