Haemaphysalis longicornis는 사람과 동물에게 여러 심각한 병원체를 전달하는 주요 매개체로, 한반도에 널리 분포하고 있다. H. longicornis는 Rickettsia spp., Borrelia spp., Francisella spp., Coxiella spp., 그리고 중증열성혈소판 감소증후군 바이러스 (SFTS virus) 등을 매개하는 것으로 알려져 있다. 국내에 서식하는 H. longicornis의 미생물 군집과 관련된 연구는 많이 진행되지 않은 것으로 확인되었다. 이 연구는 한반도 내 다양한 지역에서 채집된 H. longicornis의 미생물군집 다양성을 지역별, 성장 단계 및 성별에 따라 분석하였다. 2019년 6월부터 7월까지 질병관리청 권역별기후변화매개체감시거점센터 16개 지역에서 채집한 H. longicornis의 16S rRNA 유전자 V3-V4 영역을 PCR로 증폭 후 Illumina MiSeq 플랫폼으로 시퀀싱하였다. Qiime2를 활용한 미생물 다양성 분석을 통해 총 46개의 샘플에서 1,754,418개의 non-chimeric reads를 얻었으며, 평균 126개 의 operating taxonmic unit (OTU) 을 식별하여 총 1,398개의 OTU를 확인하였다. 대부분의 지역에서 Coxiella spp.가 우점종으로 나타났으며, 특히 Coxiella endosymbiont는 가장 높은 우점도를 보이며, Coxiella burnetii와 계통 발생 학적으로 유사한 것으로 확인되었다. 이 연구를 통해 분석된 결과는 각 지역의 H. longicornis 미생물군집 데이터 베이스 구축에 활용되었으며, 이를 통해 지역별 미생물군집의 특이성을 식별할 수 있게 하였다. 이는 한반도의 H. longicornis에 의한 질병 전파 연구와 이를 통한 공중보건 개선에 기여할 것으로 기대된다.

농촌진흥청 국립원예특작과학원에서는 2021년 분홍색계 소 형 호접란 ‘Arihong’을 육성하였다. 2014년 밝은 분홍색 소형 품종 Phalaenopsis ‘Wedding’와 백색 바탕에 분홍빛을 가지는 소형종 P. ‘[{KT1398-1×(KM-6)-4}×Chiangbeauty-88]-23’ 를 모본과 부본으로 교배하였다. 2018년 실생 120개체 중 잎자세, 화색, 화형, 꽃대수 등 특성이 우수한 ‘14104-1’ 개체를 선발하여 기내 화경배양을 통해 증식하였다. 2018년부터 2021년에까지 1차, 2차특성검정을 통해 품종의 안정성과 균일성을 확인한 후 ‘Arihong’로 명명하였다. 이 품종은 백색(WG155B) 바탕에 중앙 에는 보라빛 분홍색(PVG80B)을 띄며, 진한 자주색(PG78A) 순판 을 가지는 것이 특징이다. 꽃대가 2대씩 발생하고 꽃대 길이는 평균 42.1cm 소형 분화로 적절한 크기를 가지고 있다. 평피기 형태의 꽃은 길이와 폭이 각각 5.1, 5.7cm이며, 분지가 발생하여 1개의 꽃대에 13.0개의 소화가 착생한다. ‘Arihong’의 잎은 수평으로 자라며 길이와 폭이 각각 13.0cm, 4.9cm였다. 또한 초세가 우수하고 생육 속도가 빨라 엽수 확보가 용이한 특성을 보였다.

This study evaluated a potential sterilization process that uses calcium hypochlorite (Ca(ClO)2) as a disinfectant and hydrogen peroxide (H2O2) as a neutralizing agent for monoculture processes of microalgae (Nannochloropsis oculata). The results showed that no contaminants (prokaryote) were present when the Ca(ClO)2 concentration was greater than 0.010%. The use of an equivalent amount of H2O2 completely neutralized Ca(ClO)2 and had an additional bactericidal effect because of the formation of singlet oxygen. No substantial difference was observed in the biomass accumulation and chlorophyll contents compared to those in cultures sterilized using conventional physical methods such as autoclaving. Therefore, chemical sterilization using Ca(ClO)2 and H2O2 has an excellent economic advantage, and we expect the proposed ecofriendly chemical sterilization method to become a critical culture technology for microalgae-related industrialization.

Bentonite has been considered as a buffer material in a deep geological repository for high-level radioactive waste (HLW). Bentonite may come into contacted with various chemical solutions during the long-term storage. In particular, solutions containing K+ can affect stability of bentonite (e.g., illitization). The bentonite can be gradually saturated with the inflow of groundwater, and the temperature can rise simultaneously due to the decay of HLW. This study aimed to evaluate the bentonite stability in contacted with very highly concentrated K+ solutions with different pHs at 150°C. Batch reaction tests using KJ-II bentonite were performed for 30–150 days in teflon-stainless steel reactors. De-ionized (DI) water (pH = 6.0) and 1 M KCl (pH = 6.0), and 1 M KOH (pH = 12.5) solutions were used as reaction solutions. After completing batch reaction tests, the reacted samples were analyzed using various analytical techniques. For DI water, chemical, mineralogical, and physicochemical properties of reacted samples were similar to those of unreacted samples. For 1 M KCl solutions, cation exchage for Ca by K and slight changes in mineralogical properties of reacted samples were observed, but there are no significant changes in the physicochemical properties. In contrast, for 1 M KOH solutions, changes in chemical, mineralogical, and physicochemical properties of reacted samples were observed. Results of X-ray diffraction (XRD) analysis indicated dissolution of montmorillonite and formation of zeolite minerals, which were confirmed by thermogravimetricdifferential thermal analysis (TGA-DTA) and fourier transform infrared (FTIR) analysis. These results suggest that highly concentrated K+ (1 M) solution combined with high pH (12.5) and high temperate (150°C) may affect bentonite alteration. These prelimiary experiments were intended to qualitatively evaluate the mechanism and influncing factors of the buffer material alteration under extreme experimental conditions, and it is revealed that the conditions do not reflect the actual repository environment.

This study aimed to analyze a high-performance liquid chromatography (HPLC) separation using a pentafluorophenyl column of parent drug hydroxychloroquine (HCQ) and its active metabolite, desethylhydroxchloroquine (DHCQ) applying to determine bioequivalence of two different formulations administered to patients. A rapid, simple, sensitive and specific liquid chromatography-tandem mass spectrometry (LC-MS/MS) method has been developed and validated for bioanalysis of HCQ and its metabolite DHCQ in human whole blood using deuterium derivative hydroxychloroquine-D4 as an internal standard (IS). A triple-quadrupole mass spectrometer was operated using electrospray ionization in multiple reaction monitoring (MRM) mode. Sample preparation involves a two-step precipitation of protein techniques. The removed protein blood samples were chromatographed on a pentafluorophenyl (PFP) column (50 mm × 4.6 mm, 2.6 μm) with a mobile phase (ammonium formate solution containing dilute formic acid) in an isocratic mode at a flow rate of 0.45 mL/min. The standard curves were found to be linear in the range of 2 – 500 ng/mL for HCQ; 2 – 2,000 ng/mL for DHCQ in spite of lacking a highly sensitive MS spectrometry system. Results of intra- and inter-day precision and accuracy were within acceptable limits. A run time of 2.2 min for HCQ and 2.03 min for DHCQ in blood sample facilitated the analysis of more than 300 human whole blood samples per day. Taken together, we concluded that the assay developed herein represents a highly qualified technology for the quantification of HCQ in human whole blood for a parallel design bioequivalence study in a healthy male.

The Asian corn borer, O. furnacalis (Crambidae) and the old world bollworm, H. armigera (Noctuidae) simultaneously cause ear damage in corn in Suwon area. It has been assumed that the second generation of larvae of both insects is responsible for the damage. We, therefore, studied proper spray timing of insecticide in order to reduce the damage. A waxy corn hybrid cultivar, Ilmichal, was sown directly on four plots of a field at April 10, April 20, May 4, and May 18, 2018, respectively. A sodium channel blocker, indoxacarb, was sprayed eight times at 3- or 4-day intervals around the silking stage of corn in each sowing plot. At ear harvest time of each plot, we investigated damaged ratio and length of ear, and the numbers of both insect species. The significantly effective spray timings on reduction of ear damage were the sprays at June 29 and July 2 in the plot sown at April 10, the sprays from July 2 to 13 in the April 20-sown plot, the sprays from July 2 to 19 in the May 4-sown plot, and the sprays at July 19 in the May 18-sown plot, respectively. The damage level was positively related to the insect number. The result indicated that the spray at the silking stage of corn was effective on reduction of ear damage. It was assumed that occurrence time of neonate larvae of the insects at silking stage cause the damage, based on the experimental results using screened pots inoculated with the two species.

This study was conducted to evaluate the the efficacy of mulberry cake mixed diet on larval growth of Protaetia brevitarsis. As a result of adding 3, 5, and 10% mulberry cake to the fermented mulberry sawdust, the development period of the Protaetia brevitarsis larvae was 44.9days, 44.6days, and 41.8days, and the highest weight of larvae was 2.76g, 2.80g, and 2.89g, respectively. As a result of adding 3, 5, and 10% mulberry cake to the fermented oak sawdust, the development period of the Protaetia brevitarsis larvae was 46.7days, 41.6days, and 41.7days, and the highest weight of larvae was 2.65g, 2.65g, and 2.56g, respectively.