Macrosiphini is the most largest group in aphids, comprising near half of the described aphid species. The existence of Macrosiphini could be related to host alternation and various life cycle. Since the phylogenetic relationship of the tribe Macrosiphini has been still controversial, we analyzed Bayesian phylogeny (BP) and Maximum-likelihood (ML) based on molecular data (cytochrome oxidase I, tRNA-leucine+cytochrome oxidase II, 16S ribosomal RNA and elongation factor-1 alpha gene), and compared with the Shaposhnikov (1998) 's subtribal division: Macrosiphina, Myzian, Anuraphidina and Liosomatinae. Analyses for host range association with the morphological characters (e.g. Siphunculus and antennal tubercle on head) correspond to the tendency of host range radiation in the tribe Macrosiphini.

Acquisition of a reference Tetranychusstrains that are completely susceptible to acaricides and retain identical genetic backgrounds to acaricide-resistant strains is an essential step in elucidating mechanisms of resistance. To establish both completely susceptible and acaricide-resistant strains for this purpose, I collected Tetranychus mite populations from various regions in South Korea including both heavily cultivated and remote regions. Suitability as a susceptible or resistant reference strain was tested by determining species identity as Tetranychus urticae along with baseline susceptibility to common acaricides. The majority of mite populations collected from cultivated areas belonged to a monophyletic group of the previously reported green-type T. urticae as determined by mtCOI- and ITS2-based phylogenetic analysis. These strains showed relatively reduced levels of susceptibility to the acaricides tested, suggestive of the development of resistance. Among them, the AbaR strain was classified as a minor group in the T. urticae complex. The UD strain, originally collected from a remote island region, was found to be susceptible to the acaricides tested and generated an independent phylogenetic branch. The UD strain was also considered a minor group in the T. urticae complex. Phenotypic analysis based on morphological characters confirmed that both the AbaR and UD strains were statistically undistinguishable from the major green-type T. urticae. Taken together, I propose that the UD strain be used as a susceptible reference strain as it provides baseline susceptibility to acaricides and a wild-type genetic background for the resistance studies.

A new species of Adoxophyes unique from other closely resembling species was discovered based on molecular characters. Larvae of this species were collected from sweet cherry (Prunus avium) imported from China and intercepted under plant quarantine inspection at Korean sea and airport in 2008. They were reared to adult in the laboratory for accurate identification. We also collected two specimens from China for this study. In addition, we conducted a comparative study of three related Korean species (A. orana, A. honmai, and A. paraorana (= orana-like)) to confirm the identity of new species. We compared DNA barcoding sequences (~658 bp) of the mitochondrial cytochrome c oxidase subunit I (COI) gene from 13 specimens of four Adoxophyes species. We also compared variable internal transcribed space region 1 (ITS 1) nuclear rDNA sequence for further identification. As a result of this study, we confirmed the identity of Adoxophyes a new species. We also provided pairwise p-distances among the species and their neighbor-joining tree.

Background : Medicinal crop has been used in the traditional Asian medicinal methods. From ancient times, various kinds of medicinal crop are being cultivated in East Aisa including Korea, China and Japan. In Korea, they used a variety of medicinal plants in folk medicine and oriental medicine since ancient times. Molecular markers can be widely used in a variety of settings such as effective-loci estimation, genetic-diversity characterization, allelic-effect studies, gene-flow studies, quantitative-trait locus (QTL) mapping, and evolutionary studies. The genetic analyses of crops require large numbers of useful molecular markers for genetic or QTL identification, comparative mapping and breeding. Studying the genetic diversity and genetic relationship of crops can assist breeders. Crop genetics within a breeding program enable the economic and effective cultivar development. We tried to develop a variety of molecular markers from Angelica gigas genomic sequences for genetic studies and breeding. Methods and Results : A. gigas resources cultivated in Republic of Korea were collected. Fresh leaves were ground with liquid nitrogen and gDNA was extracted using a DNeasy Plant Mini kit (Qiagen, Valencia, CA, USA). We sequenced the whole genomes of five A. gigas accessions using Illumina HiSeq 2500 platform and identified genomic Simple Sequence Repeat (SSR) and InDel markers. DNA amplification was conducted using the PCR system (Bio-Rad T-100 Thermal Cycler). PCR products were separated by capillary electrophoresis on the ABI 3730 DNA analyzer (Applied Biosystems) and Fragment analyzer automated CE system (Advanced Analytical Technologies, Ankeny, IA, USA). Conclusion : We developed novel SSR and InDel markers from A. gigas genomic sequences for further genetic studies and breeding.