Golden apple snails(GAS) are native to warm regions such as Central and South America and Southeast Asia, and were first introduced as a high-protein food. GAS are omnivorous and have a habit of eating plants submerged in water, so they have been used for eco-friendly weed control in rice fields since 1992. When the GAS was first introduced, it was thought that it would be impossible to overwinter in Korea. However after 2000, overwintering individuals were founded and damage to rice occurred and the development of means to control GAS has been required. In this study, we tested the effectiveness of an eco-friendly pest control agent using Styrax japonicus that grow naturally in Korea. As a result of exposing GAS to S. japonicus fruit powder, a 100% molluscicidal effect was confirmed at 66.7ppm. To investigate the duration of effect, treatment was performed at the same concentration and molluscicidal effect of more than 90% was up to 3 days after treatment. The killing effect of each part of the S. japonicus was compared, and the seed extracts showed no killing effect at all concentrations, while the sarcocarp extracts showed a 100% killing effect up to 33.3ppm, and the fruit extracts showed a 100% killing effect up to 200ppm.

The fall armyworm (FAW), Spodoptera frugiperda (Lepidoptera: Noctuidae), which is native to tropical and subtropical regions of the Western Hemisphere is now annually arrives in Korea. In this study, we developed loop-mediated isothermal amplification (LAMP) assay, one of the main merits of which is a rapid identification of target species. Five among 11 FAW-specific loci tested successfully provided a consistent reaction when ten FAWs, which were collected from eight localities in four countries were tested, whereas the 13 non-target species were not amplified. To increase in-field applicability of the method all life stages, reaction time, and different periods after death was tested using the quick extracted DNA. Our FAW diagnostic protocol can be completed within 30 min, from the process of extracting genomic DNA from an egg or a 1st instar larva to species determination.

지난 2022년 제주도 애월읍 일대에서 콩 해충으로 알려진 콩은무늬밤나방(Ctenoplusia agnata) 성충이 검거세 미밤나방(Agrotis ipsilon)의 성페로몬 트랩에 대량으로 포획되었다. 검거세미밤나방 트랩은 목적 해충에 대한 포획 효율을 조사하기 위해 세 구성 성분, (Z)-7-dodecenyl acetate, (Z)-9-tetradecenyl acetate를 3:1 비율로 고정하고 (Z)-11-hexadecenyl acetate를 0, 1, 6, 10, 15로 각각 비율을 달리한 미끼를 사용하였다. 각 조성별 콩은무늬밤나방 성충 포획수를 비교한 결과, (Z)-11-hexadecenyl acetate가 첨가되지 않은 트랩에서 주당 평균 약 17.96마리로, 가장 많은 수의 개체가 포획된 것으로 확인되었다. 반면, (Z)-11-hexadecenyl acetate가 가장 많이 함유된 트랩에서 주당 평균 약 2.5마리로 가장 적은 개체가 포획된 것으로 파악되었다. 이에 (Z)-11-hexadecenyl acetate의 비율이 증가할 수록, 포획되는 콩은무늬밤나방의 개체 수가 감소되는 것을 확인할 수 있었다. 검거세미밤나방 미끼의 주성분인 Z)-7-dodecenyl acetate는 기존의 콩은무늬밤나방 유인 성분 중 하나이기도 하여 해당 성분의 구성비가 유인에 영향을 미쳤다는 것을 예측할 수 있다. 추후에 해당 트랩들과 시판 중인 콩은무늬밤나방 성페로몬 트랩을 설치하 여 포획 양상을 비교할 필요성이 요구된다.

Pesticides are indispensable in contemporary agriculture but are mainly attributed to honey bee population decline. In order to understand the approximate physiological response to pesticides, honey bees were exposed to seven pesticides (Acetamiprid, Imidacloprid, Flupyradifurone, Carbaryl, Fenitrothion, Amitraz, and Bifenthrin), and expression changes of the genes categorized into four physiological functions (insecticide targets, immune-, detoxification-, and reactive oxygen species response-related gene) were analyzed in the head and abdomen of honey bee exposed to pesticides using quantitative PCR. Based on the heat map analysis, immune-related genes seem to be more up-regulated by pesticide exposure in head than abdomen. Among detoxification genes, only cytochrome P450 families were up-regulated in head. Interestingly, regardless of the insecticide target, expressions of Nicotinic acetylcholine receptor beta 1 and Acetylcholinesterase 1 were notably induced by pesticide exposure in head. Heat map analysis expressing the transcription profiles of various genes in the head and abdomen of the honey bee exposed to various pesticides can be used to diagnose pesticide damage in honey bees in the future.

The adult of honey bee, Apis mellifera, performs an age-dependent division of labor with nurse bees and foragers. Foragers fly outside the hive to collect pollen and nectar, while nurses feed and care for the larvae and queen inside the hive. Foragers are considered to be frequently exposed to agrochemicals, although nurses, stayed inside the hive, are potentially exposed to pesticides through application of miticides and pesticidecontaminated food provided by forager. Therefore, physiological effects of pesticides to nurses should be elucidated to understand the adverse effects of the chemicals on entire honey bee colony. In this study, we investigated the expression changes of the genes associated with labor division (task genes) and the nursing behavior of nurse bees fed four pesticides: acetamiprid (ACE), carbaryl (CB), imidacloprid (IMI), and fenitrothion (FEN). When nurses were exposed to ACE, IMI, and FEN, expression levels of task genes were up- and down-regulated, and their nursing behaviors were also suppressed and enhanced, respectively. CB did not alter the gene expression levels, however increased nursing behavior. These suggest the potential of pesticide that breaks the balance of labor distribution in honey bee colony.

The utilization of methyl bromide (MB) for quarantine purposes has been hampered by its designation as an ozone-depleting substance under the Montreal Protocol. The International Plant Protection Convention's (IPPC) call for alternatives to MB and a reduction in its usage. There is an urgent need to explore and implement substitutes. Despite some substitute agents like EDN being developed for wood, EDN has been limited due to various factors such as occupational risks. This study focuses on evaluating the efficacy of Sulfuryl Fluoride (SF) as a viable alternative fumigant against Reticulitermes speratus, one of major wood destroying pests. Experimental trials conducted at ambient temperature (23°C) revealed promising results, with SF demonstrating LCT50 and LCT99 values of 30.87 mg·h/L and 42.53 mg·h/L, respectively. Under low-temperature conditions (5°C), SF remained effective but with slightly higher LCT50 and LCT99 values of 151.62 mg·h/L and 401.90 mg·h/L, respectively. The penetration test, conducted using R. speratus-infested pine wood cubes, further highlighted SF's efficacy, with LCT50 and LCT99 values of 31.59 mg·h/L and 53.34mg·h/L at 23°C, indicating powerful penetration capabilities. When tested at a loading ratio of 90% (v/v) at 5.0mg/L for 24 hours in a 500L chamber as a middle-scale trial, SF achieved a 100% mortality, showing its potential as a suitable replacement for MB. These findings suggest that SF could open new markets as an MB substitute and enhance safety at quarantine sites when applied to imported and exported timber.

Immune priming is an increased immunity after prior exposure to a specific pathogen as a kind of adaptive immunity and occurs in insects. However, its underlying mechanism is elusive in insects. Immune priming was detected in a lepidopteran insect, Spodoptera exigua. Prior infection with a heat-killed pathogenic bacterium, Xenorhabdus hominickii, increased survival upon the second infection of the live bacteria compared to larvae without pre-exposure. Plasma collected from larvae with the prior infection significantly up-regulated cellular and humoral immune responses compared to the similar treatment without prior exposure. However, when the active plasma exhibiting immune priming was heat-treated, it lost the priming activity, suggesting a presence of protein factor(s) in the immune priming. Lipocalin is a lipid carrier protein and is well known in vertebrates for diverse physiological functions including immunity. An apolipoprotein D3 (ApoD3) is known to be a lipocalin functioning in immune priming in a mosquito, Anopheles gambiae. A homologous ApoD3 (Se-ApoD3) was identified in S. exigua. Se-ApoD3 was expressed in all developmental stages and larvae, it was highly expressed in hemocytes. RNA interference (RNAi) of Se-ApoD3 expression was performed by injecting its specific dsRNA. The larvae treated with the RNAi were impaired in cellular and humoral immune responses. Furthermore, the plasma collected from RNAi-treated larvae lost the immune priming even at the prior exposure. These suggest that Se-ApoD3 mediates the immune priming in S. exigua.

Silene fissipetala Turcz., which is native to Continental China and Taiwan, was newly found in Chungcheongnam-do, Korea. S. fissipetala is similar to the related taxa S. antirrhina L., S. armeria L., and S. koreana Kom. in that it has glutinous zones. However, S. fissipetala is distinguished from the congeneric species by the presence of laciniate at the petals. The species grows on slopes and roadsides, suggesting that it is likely to have been introduced through the installation of green sites and road construction. A precise description, photographs, voucher specimens and a key to related taxa are provided.

This study was aimed to isolate bacterial inoculants producing chitinase and evaluate their application effects on corn silage. Four corn silages were collected from four beef cattle farms to serve as the sources of bacterial inoculants. All isolates were tested against Fusarium graminearum head blight fungus MHGNU F132 to confirm their antifungal effects. The enzyme activities (carboxylesterase and chitinase) were also measured to isolate the bacterial inoculant. Based on the activities of anti-head blight fungus, carboxylesterase, and chitinase, L. buchneri L11-1 and L. paracasei L9-3 were subjected to silage production. Corn forage (cv. Gwangpyeongok) was ensiled into a 10 L mini silo (5 kg) in quadruplication for 90 days. A 2 × 2 factorial design consists of F. graminearum contamination at 1.0104 cfu/g (UCT (no contamination) vs. CT (contamination)) and inoculant application at 2.1 × 105 cfu/g (CON (no inoculant) vs. INO (inoculant)) used in this study. After 90 days of ensiling, the contents of CP, NDF, and ADF increased (p<0.05) by F. graminearum contamination, while IVDMD, acetate, and aerobic stability decreased (p<0.05). Meanwhile, aerobic stability decreased (p<0.05) by inoculant application. There were interaction effects (p<0.05) on IVNDFD, NH3-N, LAB, and yeast, which were highest in UCT-INO, UCT-CON, CT-INO, and CT-CON & INO, respectively. In conclusion, this study found that mold contamination could negatively impact silage quality, but isolated inoculants had limited effects on IVNDFD and yeast.

본 연구는 금속 인공물을 감소시키기 위한 VAT(view angle tilting)와 SEMAC(slice encoding for metal correction) 기법 적용에 따른 온도 변화 범위를 관찰하고자 하였다. 제작된 인체 모방 팬텀을 활용하였고, 검사방법으로는 임상에서 실제로 사용하고 있는 고속스핀에코(fast spin echo, FSE) 기법의 영상 파라미터들을 그대로 이용하였다. VAT 와 SEMAC 기법은 FSE와 같은 파라미터로 설정한 다음 VAT 파라미터는 100%와 SEMAC 파라미터는 25로 설정하였다. 온도 측정 방법으로는 수소원자 공명주파수전이법(proton resonance frequency shift, PRFS)기법을 활용하였으며, 광 섬유 온도계(fiber-optic sensor, FOS)로 절대 온도를 측정한 후 비교 분석하였다. 온도 변화는 SEMAC 기법에서 기존 FSE 기법 (0.28℃±0.10℃)에 비해 1.63℃±0.12℃로 약 6배 상승하였고(SEMAC-FOS = 1.59℃), VAT 기법은 약 2배 증가(VAT-FOS = 0.51℃)가 확인되었다. 특히, SEMAC 기법은 VAT 기법(VAT-FOS = 0.51℃, VAT-PRFS = 0.54℃ ±0.02℃)과 비교하여 약 3배가 증가하여 가장 높은 온도 상승이 관찰되었다. 이는 SEMAC 기법 적용 시 자기공명영상 전자파 인체 영양에 대한 안전기준을 충족하기 위해 영상 파라미터 최적화 작업의 필요성을 시사한다.

In the realm of dental prosthesis fabrication, obtaining accurate impressions has historically been a challenging and inefficient process, often hindered by hygiene concerns and patient discomfort. Addressing these limitations, Company D recently introduced a cutting-edge solution by harnessing the potential of intraoral scan images to create 3D dental models. However, the complexity of these scan images, encompassing not only teeth and gums but also the palate, tongue, and other structures, posed a new set of challenges. In response, we propose a sophisticated real-time image segmentation algorithm that selectively extracts pertinent data, specifically focusing on teeth and gums, from oral scan images obtained through Company D's oral scanner for 3D model generation. A key challenge we tackled was the detection of the intricate molar regions, common in dental imaging, which we effectively addressed through intelligent data augmentation for enhanced training. By placing significant emphasis on both accuracy and speed, critical factors for real-time intraoral scanning, our proposed algorithm demonstrated exceptional performance, boasting an impressive accuracy rate of 0.91 and an unrivaled FPS of 92.4. Compared to existing algorithms, our solution exhibited superior outcomes when integrated into Company D's oral scanner. This algorithm is scheduled for deployment and commercialization within Company D's intraoral scanner.