장미 ‘Sahara’는 국립원예특작과학원에서 2022년에 육성한 분홍톤 아이보리 스프레이 장미 품종으로 2013년 빨간색 스프레 이 품종 ‘Fangfare’에 아이보리색 스프레이 품종 ‘Vivien’을 부본으로 인공 교배 하였다. 총 73개의 교배 실생을 얻었으며 2015년부터 1, 2, 3차 특성검정을 통해,화색과 화형이 안정적이 며 생산성 및 절화 특성이 우수한 ‘원교 D1-360’을 최종 선발하 여 2022년 ‘Sahara’로 명명하고 국립종자원에 품종보호 출원· 등록하였다(등록번호 제9771호). 장미 ‘Sahara’ 품종은 분홍톤 크림색(155D)의 꽃잎수는 71.5매인 겹꽃으로 화폭과 화고는 각각 4.9, 3.1cm이며 소화수가 7.4개/줄기인 스프레이 장미이 다. 장미 ‘Sahara’ 품종의 절화장은 평균 73.8cm로 대조 품종 ‘Pink shin’56.9cm 대비 길며, 절화 수명은 약 17.8일로 ‘Pink shin’ 15.6일 보다 2일 정도 길다. ‘Sahara’는 절화 생산량은 연간 168본/m2로 ‘Pink Shine’ 140본 대비 생산량이 많다. 전자코를 이용한 PCA분석결과 주성분1과 2는 각각 99.3%와 0.6%로 전체 변이량의 99.9%를 반영하고 있다. Rader plot 분석결과 P10/2,P40/1 및 T30/1 센서 반응이 높았으며 총 6개 센서에서 모두 ‘Sahara’는 대조품종 ‘Pink Shine’에 비해 반응이 낮았다. 절화용 스프레이 장미 ‘Sahara’ 품종은 파스텔톤 의 중형 소화로, 균일한 절화 품질 및 우수한 수량으로 재배농가 의 선호도가 높아 국내에서 많이 재배될 것으로 기대된다.

The balloon flower (Platycodon grandiflorum A. DC.) is a medicinal and perennial flowering plant. Jangback is an important white-flower type balloon flower cultivar registered in South Korea, but no molecular marker was available to differentiate it from other white-flower lines. Therefore, we evaluated five P. grandiflorum white-flower lines and identified a single nucleotide polymorphism (SNP) derived from the chloroplast TrnL-F genomic sequence that specifically differentiated Jangback from the other four genotypes. Cultivar identification was achieved by detecting allelic variations of the SNP using amplification refractory mutation system-polymerase chain reaction (ARMS-PCR) analysis and high resolution melting (HRM) curve analysis. The present study describes a rapid and reliable method to authenticate the medicinally and economically valuable white-flower Jangback cultivar. Our results indicate that the plastid TrnL-F region provides for marker assisted identification and selection in intraspecific polymorphism studies, thereby the identified SNP marker provides a robust tool along with ARMS-PCR and HRM curve analysis for rapid and efficient identification of the medicinally valuable Jangback cultivar.

We investigated the effects of fluctuating temperature on development and fertility of M. persicae at different temperature conditions, 10, 15, 20, 25, 28, and 30±5℃, respectively. In this study, we collected detailed data on development periods, and fertility of M. persicae at six different temperatures. We analyzed the life table parameters of M. persicae using age-stage, two-sex life table program. The intrinsic and finite rate of increase were the highest at 25±5℃. The fertiltiy was the highest at 20±5℃.

This study focused on the genomic analysis of Anopheles kleini and Anopheles pullus, both vectors of vivax malaria within the Anopheles Hyrcanus group. Using Illumina NovaSeq600 and Oxford Nanopore platforms, we identified 126 and 116 contigs, along with 40,420 and 32,749 genes from An. kleini and An. pullus, respectively. The assembled genome sizes were 282 Mb for An. kleini and 247 Mb for An. pullus, which are within a similar range to the sizes previously estimated by digital PCR (249 Mb and 226 Mb). We are currently also estimating the genome sizes of other Anopheles spp. and manually curating key genes determining vectorial capacity.

The Spectro-Photometer for the History of the Universe, Epoch of Reionization and Ices Explorer (SPHEREx) will provide all-sky spectral survey data covering optical to mid-infrared wavelengths with a spatial resolution of 6.′′2, which can be widely used to study galaxy formation and evolution. We investigate the galaxy-galaxy blending in SPHEREx datasets using the mock galaxy catalogs generated from cosmological simulations and observational data. Only ∼0.7% of the galaxies will be blended with other galaxies in all-sky survey data with a limiting magnitude of 19 AB mag. However, the fraction of blended galaxies dramatically increases to ∼7–9% in the deep survey area around the ecliptic poles, where the depth reaches ∼22 AB mag. We examine the impact of the blending in the number count and luminosity function analyses using the SPHEREx data. We find that the number count can be overestimated by up to 10–20% in the deep regions due to the flux boosting, suggesting that the impact of galaxy-galaxy blending on the number count is moderate. However, galaxy-galaxy blending can marginally change the luminosity function by up to 50% over a wide range of redshifts. As we only employ the magnitude limit at Ks-band for the source detection, the blending fractions determined in this study should be regarded as lower limits.

Fungal contaminant in the indoor air is one of risk factors that could damage valuable paper-based records preserved in libraries. In the process of monitoring airborne fungi at the Nara Repository, the National Archives, Seoul, Korea, three fungal strains, DUCC 16098, DUCC 17764, and DUCC17767 were isolated from the archive’s air samples. Fungal identification was performed based on the morphological characteristics and phylogenetic analysis of the internal transcribed spacer (ITS), the 28S LSU rDNA, and β-tubulin gene (BenA), and TEF1-α gene. These DUCC 16098, DUCC 17764 and DUCC17767 strains were identified as Clonostachys farinosa, Penicillium cosmopolitanum, and Cephalotrichum purpureofuscum. These species have not been recorded before in Korea. Information on these fungi will help the monitoring and management of airborne fungi in the archival facilities.

We investigated the functional response of aphid parasitoid, Aphidius colemani Viereck (Hymenoptera: Braconidae), on the green peach aphid, Myzus persicae (Sulzer) (Hemiptera: Aphididae) at four different constant temperatures (15, 20, 25 and 30℃). Seven host densities (2, 4, 8, 16, 32, 64, and 128) were used during a 24-h period. A type III functional response for A. colemani was fit separately at each constant temperature. The estimated handling times at 15, 20, 25, and 30℃ were 0.85, 0.61, 0.41 and 0.88 day, respectively. The proportion of aphids that were parasitized showed the similar characteristics curve at four different constant temperatures.

Expression changes of stress-induced peroxidase (swpa2 and swpa4) and storage root-specific sporamin (spo-A and spo-B) genes were examined using qRT-PCR after treatment with wounding and bacterial pathogens on leaves of sweetpotato (Ipomoea batatas) plants. As a result of examining the expression change in the wounding treatment condition for 48 hours after treatment, which is a representative physical stress, the expression of all genes increased after 12 hours of wounding treatment, but the expression pattern of each gene group showed distinct differences thereafter. Expression levels of swpa2 and swpa4 strongly increased up to 36 or 48 hours after wounding treatment, whereas spo-A and spo-B expression levels strongly decreased after 24 or 36 hours after wounding treatment. Peroxidase and sporamin genes are involved in the early response after wounding treatment and, in particular, the peroxidase swpa2 and swpa4 genes are also involved in the late response after wounding treatment. Gene expression analysis after infection with P. chrysanthemi, which causes softness in sweetpotato, showed that the swpa2 and swpa4 genes were weakly induced after 8 hours and then strongly induced after 20 hours during pathogen infection. Expression of the spo-A gene was weakly induced in the pathogen-treated group after 20 hours, whereas spo-B showed an expression pattern similar to that of the peroxidase genes. The above results indicate that expression of the stress-induced peroxidase gene used in this study is induced not only by abiotic stress but also by biological stress caused by bacterial pathogen invasion and that peroxidase plays an important function in the initial defense response.

A pregnancy diagnosis is an important standard for control of livestock’s reproduction in paricular dairy cattle. High reproductive performance in dairy animals is a essential condition to realize of high life-time production. Pregnancy diagnosis is crucial to shortening the calving interval by enabling the farmer to identify open animals so as to treat or re-breed them at the earliest opportunity. MicroRNAs are short RNA molecules which are critically involved in regulating gene expression during both health and disease. This study is sought to establish the feasible of circulating miRNAs as biomarkers of early pregnancy in cattle. We applied Illumina small-RNA sequencing to profile miRNAs in plasma samples collected from 12 non-pregnant cows (“open” cows: samples were collected before insemination (non-pregnant state) and after pregnancy check at the indicated time points) on weeks 0, 4, 8, 12 and 16. Using small RNA sequencing we identified a total of 115 miRNAs that were differentially expressed weeks 16 relative to non-pregnancy (“open” cows). Weeks 8, 12 and 16 of pregnancy commonly showed a distinct increase in circulating levels of miR-221 and miR-320a. Through genome-wide analyses we have successfully profiled plasma miRNA populations associated with pregnancy in cattle. Their application in the field of reproductive biology has opened up opportunities for research communities to look for pregnancy biomarker molecules in dairy cattle.

Cryopreservation is used for blastocyst preservation of most mammalian embryos and is an important technique for breeding. We aimed to compare the efficiency of the cryopreservation method using the standard Cryotop device and the ReproCarrier device, a domestic product manufactured in Korea. The efficacy of the two devices was analyzed based on the survival rate, intracellular levels of reactive oxygen species (ROS), and apoptosis of the vitrified bovine blastocysts. The survival rates of the vitrified-warmed blastocysts were similar between the ReproCarrier group (58.4 ± 17.7%) and Cryotop group (59.9 ± 14.1%). Intracellular ROS levels and apoptotic index were determined by DCFDA staining and TUNEL assay. Changes in intracellular ROS levels, number of total nuclei, and cellular apoptosis of vitrified blastocysts after cryopreservation were not significantly different between the two groups. These results indicate that the ReproCarrier device method is as effective as the standard Cryotop method for vitrification of bovine blastocysts in vitro.

Radioisotope ADME (RI-ADME) studies are enabling visualization of the biodistribution in molecular imaging. We applied RI-ADME to investigate the tumor targeting capacity and biodistribution of trastuzumab-monomethyl auristatin F (LCB14-0110) in JIMT-1 xenograft mice and healthy marmoset. The LCB14-0110 was labelled with 125I. 125I-LCB14-0110 was intravenously administered to the animals. The gamma-count and single-photon emission computed tomography/computed tomography (SPECT/CT) was conducted for biodistributioon and bioimaging of the biopharmaceutics. Tumor uptake in xenograft mice was highest at three-day after 125I-LCB14-0110 administration in both the biodistribution and SPECT/CT bioimaging. Alternatively, blood and organ tissues showed gradual decrease in radioactivity over time. In marmosets, radioactivity in all organ tissues rapidly reduced and no specific targeting of organs was observed in the biodistribution study and SPECT/CT imaging. Hence, 125ILCB14- 0110 demonstrated effective tumor targeting capacity and accumulated in JIMT-1 cell-bearing mice. However, accumulation did not occur in the organs of xenograft mice. Additionally, marmosets showed rapidly decrease in radioactivity throughout the entire body without accumulation in the normal organs. We also confirmed that the drug distribution was similar in normal organs between the two experimental animal species except spleen. Therefore, 125I is expected to be a useful tool in the study of RI-ADME in biopharmaceuticals through minimal antibody modification.