사용후핵연료의 효율적인 관리를 위하여 원자력연구소에서 개발중인 사용후핵연료 차세대관리 종합공정(ACP)은 공정타당성연구 단계를 마치고 이의 실증을 위한 - type핫셀 건설 단계에 이르렀다. 핫셀의 설계에 앞서 사용후핵 연료를 취급하게 되는 과정에서 발생할 수 있는 방사능에 대한 환경영향평가를 정상운전 시와 사고발생 시로 나누어 수행하였다. 평가에 필요한 자료들은 공정의 개념설계 보고서와 최근 연구소부지 기상 테이터 및 부지특성 자료를 바탕으로 하였으며 기존의 유사한 시설에 대한 평가방법을 참조하였다. 각 핵종별 발생량과 방출량을 계산하여 피폭선량을 계산하였으며 평가결과 원자력법관련 규제기준과 핫셀이 위치하게 되는 IMEF 건물의 안전성분석 기준보다 매우 안전한 결과를 얻어 시설 운영에 대한 안전성을 확보하였다.

원전에서 발생된 중저준위 방사성 폐기물의 경우 처분장으로 이송되기 이전에 드럼에 대한 세부적인 정보 특히 핵종 재고량에 대한 평가가 수행되어야 한다. 그러나 드럼처리된 방사성폐기물의 경우 평가 대상 핵종 농도에 대한 예측이 어려운 것이 일반적이다. 따라서 이를 극복하고자 직접측정이 어려운 경우 척도인자 방법을 활용하고 있다. 국내의 경우 1996년부터 고리원전에서 척도인자 개념이 적용된 핵종분석장치를 운영해오고 있다. 그러나 고리원전에 적용된 척도인자의 경우 많은 개선의 여지가 남겨져 있다. 따라서 현재 척도인자의 향상을 위한 연구가 진행 중에 있다. 본 논문에서는 연구의 범위에 대한 개략적인 소개와 핵종 재고량 평가 방법 중 보다 신뢰할 수 있는 평가 방법을 찾고자 통계적인 척도인자 평가 방법을 비교 평가했으며 이를 통해 고리원전에 사용된 산술평균 방법을 기하평균 방법으로 바꾸는 것이 예측의 정확성을 향상시킬 수 있을 뿐만 아니라 드럼내 핵종 재고량의 과대평가를 막고 합리적인 보수성을 유지할 수 있음을 알수 있었다.

고리 1호기 원자로압력용기의 중성자속과 방사화생성물 재고량을 계산하기 위하여 DORT 코드와 ORIGEN2 코드를 사용하였다. DORT 코드를 이용해 중성자속을 계산하기 위하여 노심을 중앙부터 원자로압력용기까지 방위각 방향으로 94 mesh로 분할하였다. 원자로압력용기 영역의 중성자속을 이용하여 주요 핵종의 단면적을 재계산하였다. 원자로압력용기의 경우, Fe, Co, Ni 및 Ni의 핵종이 총 방사능의 약 95%를 차지하였으며, 해체 후 50년 이상 냉각후의 총 방사능은 정지시점과 비교하여 약 0.2% 이하로 감소하는 것으로 평가되었다. 총 중량이 210 ton인 원자로압력용기의 총 방사능은 5.25GBq이었다. ORIGEN2 계산 결과를 검증하기 위하여 고리 1호기 원자로압력용기의 계산값과 실측값에 대한 비교 검증을 수행하였으며, 그 결과는 서로 일치함을 확인할 수 있었다.

한국원자력연구소에서는 고온의 용융염 매질 하에서 사용 후 핵연료를 환원시키는 차세대관리종합공정 연구를 수행 중에 있다. 추후 본 기술개발을 실증시험 하기 위해서는 방사선 차폐능이 확보된 핫셀이 필수적이며, 핫셀은 최대 1,385TBq의 방사능량에 대한 차폐 안전성을 가져야 한다. 최대 방사선원에 대한 핫셀의 차폐능을 확보하기 위하여, 본 연구에서는 실증시험 시 사용후핵연료부터 발생하는 중성자 및 감마선에 의한 선량률이 법적 허용선량치보다 낮게 유지되도록 핫셀의 차폐 설계에 대한 안전성을 평가하였다. QAD-CGGP 및 MCNP-4C 코드를 이용하여 핫셀 차폐체의 설계치에 대한 차폐 계산을 수행하였다. 작업구역에 대한 감마선 차폐계산 결과 QAD-CGGP 코드는 2.10, 2.97 mSv/h, MCNP-4C 코드는 1.60, 2.99 mSv/h 이었으며, 서비스 구역은 1.01, 7.88 mSv/h 로 평가되었다. 그리고 MCNP-4C코드를 이용하여 중성자에 의한 선량률을 계산한 결과, 중성자에 의한 선량률은 감마에 의한 선량률의 약 20% 이하치를 나타내었다. 따라서 선량률 대부분은 감마선에 의한 영향임을 알 수 있었다. 본 연구를 통하여 핫셀의 차폐 설계치가 작업구역의 선량 제한치 0.01 mSv/h 와 서비스 구역에서의 선량 제한치 0.15 mSv/h를 만족시키는 것을 확인할 수 있었다.

This study was carried out to compare chromosomal characteristics between Atractylodes japonica and A macrocephala. Cytogenetic analysis was conducted based on karyotype analysis and physical mapping using fluorescence in situ hybridization. As a result of karyotype analysis by feulgen staining, somatic chromosome numbers of A. japonica and A. macrocephala were 2n=24. The length. of the mitotic metaphase chromosomes of A. japonica ranged from 0.70 to 1.60μm with a total length. of 12.11μm and the homologous chromosome complement comprised six metacentrics, five submetacentrics and one subtelocentrics. On the other hand, the length of the mitotic metaphase chromosomes of A. macrocephala ranged from 0.90 to 2.35μm with a total length of 16.58μm and the homologous chromosome complement comprised seven metacentrics and five submetacentrics. The total length of A. japonica chromosomes was shorter than that of A. macrocephala, but A. japonica had one subtelocentrics (chromosomes 4) different from A. macrocepha1a. chromosomes. The F1SH technique using 17S and 5S rDNA was applied to metaphase chromosomes. The signals for 17S rDNA were detected on the telomeric regions of chromosomes 4 and 5 in both A japonica and A. macrocephala. The 5S rDNA signal was found in the short arm of chromosome 1.

The study evaluated the effect of donor cell treatments for G0/Gl synchronization and the donor ceil type on development and incidence of apoptosis in cloned cattle embryos. Primary cultures were established from a female fetus on day 50 of gestation and

Mainly due to deficiencies in nuclear reprogramming, gene expression and DNA fragmentation, which result in early and late embryonic losses, the overall success rate achieved by cloning techniques to date is low. This present study compared the incidences of DNA fragmentation during development of IVF, parthenotes (PT), nuclear transfer (NT) and transgenic (TG) embryos. Terminal deoxynucleotidyl transferase (TdT) nick-end labelling (TUNEL) with propidium iodide counter staining was used for determination of DNA fragmentation and total number, respectively. TG and NT donor cells were fetal fibroblasts with or without transfection with EGFP, and cultured in DMEM+15% FCS until confluent, for 5 days. At 19 h post-maturation (hpm), enucleated oocytes were reconstructed with donor cells and activated at 24 hpm with the combinations of ionomycin (5 M, 5 min) and cyclo-heximide (10 g/ml, 5 h) after electric fusion by a single DC pulse (1.6 KV/cm, 60 sec). Parthenotes were produced by the same activation protocol at 24 hpm. (중략)

Recently, sperm has been used as a vector to carry exogenous genes for the production of transgenic animals. However, the success in cattle is low, due to deficiencies in oocyte activation and sperm decondensation caused by high disulphide bond (S=S) content in mature sperm. This study was carried out to develop an effective method for producing transgenic animals with round spermatids (RS). Two methods of embryo production - electric fusion (EC) or intracyto-plasmic injection (IC) and three activation treatments were compared. RS were isolated from bull testes by Percoll density gradients (20, 35, 40, 45 and 90%). Fusion between ooplast and RS was performed with a single DC electric pulse (1.0 KV/cm, 45 sec) in 0.28 M mannitol solution supplemented with 100 M CaCl2 and 100 M MgCl. (중략)

The successful development of embryos cloned by nuclear transfer (NT)have been dependent on a wide range of known factors including cell cycle of donor and recipient ooplast, oocyte quality, NT procedure and oocyte activation. The present study compared the development of cloned porcine embryos following different activation treatments. Cumulus-oocyte complexes (COCs) were aspirated from 26 mm follicles of slaughterhouse ovaries and cultured for 22 h in NCSU #23 medium supplemented with 10% porcine follicular fluid, 0.57 mM cysteine, 0.5 g/mL LH, 0.5 g/mL FSH and 10 ng/mL EGF. The COCs were further cultured for an additional 22 h in the same medium at in an atmosphere of 5% in air, without hormonal supplements. Primary cultures of fibroblasts isolated from a female fetus on day 40 of gestation were established in DMEM + 15% FCS. For nuclear donation, cells at the 5th-6th passage were cultured in DMEM +0.5% FCS for 5 days in order to arrest the cells in G0/Gl. After enucleation, oocytes were reconstructed by transfer of donor cells and fusion with three DC pulses (1.4 KV/cm, 30 sec) in 0.28 M mannitol containing 0.01 mM and 0.01 mM . Eggs were then divided into three treatment groups, control (without further treatment, Group 1), eggs cultured in 10 g/ml cycloheximide (CHX) for 5 h (Group 2), and eggs cultured in 1.9 mM 6-dimethylaminopurine (6-DMAP) for 5 h (Group 3). The eggs were then cultured in sets of 30 in 60 I drops of NCSU#23 supplemented with 4mg/ml BSA (essentially fatty acid free) until day 7 at in a humidified atmosphere of 5% . On day 4 the culture were fed by adding 20 I NCSU #23 supplemented with 10% FBS. Development rates into blastocysts were significantly higher (P<0.05) in Group 3 embryos compared to Group 1 controls (, respectively), but rates did not differ in Group 2 compared to control (). Total cell number in Group 3 blastocysts was however significantly higher (P<0.05) than in Groups 1 and 2 (, respectively). These results suggest that 6-DMAP is more efficient than cycloheximide in the activation of electrically fused NT oocytes during in vitro production of cloned porcine embryos.

Telomeres are the end of chromosomes and consist of a tandem repeat sequence of (TTAGGG)n and associated proteins. Telomerase is a ribonucleoprotein which act as a template for the synthesis of telomeric DNA. Telomeres are essential for chromosome stability and are related with cell senescence, apoptosis and cancer. Even though telomeres and telomerase have been studied extensively, very little is known about telomere dynamics in embryonic cells. This study was carried out to analyze the telomeres distribution and telomerase activity of chicken cells during embryonic and developmental stages. The target cells for analysing were sperms, ovulated ova, early embryonic cells and the cells from brain, heart, liver, kidney and germinal tissue in fetus. Telomeres distribution on target cells was analyzed by Q-FISH (Quantitation-Fluorescence in situ Hybridization) techniques using a chicken telomere repeat probe. Telomerase activity was performed by TRAP assay (Telomeric repeat Amplification Protocol) with target DNA. In results, the telomeres of chicken were found at the ends of all chromosomes. In addition, chicken had interstitial telomeres on chromosomes 1, 2 and 3. Telomerase activity was highly detectable in early embryonic cells, germinal tissues and kidney cells. Whereas telomerase activity was gradually down-regulated when the organs, including brain, heart, and liver, were developed from embryos. In the distribution of telomeric DNA on the embryonic and developmental stages, most of the cells was gradually decreased in telomere quantity during ontogenesis.

The birth of the clone animals is influencing the frontier of research of animal biotechnology. It has effects on research of animal biotechnology itself by necessitating setting of new research subjects, modifications of the strategy of ongoing research projects, and challenges to schemes formerly considered impossible. In my talk, such topics including mass production of fertile ova and oocyte maturation will be discussed. (1) Oocytes are needed for the production of a clone by nuclear transplantation. Mitochondrial DNA inherited via the oocyte are involved also in the morphogenesis. Therefore, oocytes from the same animal must be used as recipients to produce genuine clones by nuclear transplantation. Experimenting on the assumption that selective oogenesis can be avoided, and apoptosis of oocytes can be prevented, by using ovarian angiogenic factos will be introduced. (2) It is important to clarify the factors of oocytes involving in reprogramming of somatic cells. Such factors are thought to be expressed in oocytes during oogenesis and oocyte maturation. Therefore, molecular mechanisms of oogenesis and oocyte maturation must be clarified extensively. Topics in this field including our recent advances will be discussed. (중략)

Seeds of burcucumber were treated with accelerated aging, cold-stratification, and light quality illuminated during desiccation to enhance their germination and seedling emergence. The germination was increased by aging and cold-stratification although the latter treatment showed greater effectiveness than the former one. In the combined treatment of aging 6 days at 45~circC and cold-stratification, the germination was promoted under longer period of cold-stratification to reach nearly 100% in 3 week cold-stratification on the ninth day from sowing. In the sequentially combined treatment of aging, cold-stratification, and light quality during 24 hour desiccation at 35~circC , no-stratified seeds showed the highest rate in red light treatment but the lowest in far-red light. This implies that the phytochrome action run during the desiccation of imbibed seeds. The red light exposure during drying for the cold-stratified seeds after aging accelerated the germination even more than the dark treatment and germinated 100% on the next day of sowing. It is concluded that the sequential treatment of aging, cold-stratification, and red light illumination during desiccation can highly promote percentage and speed of burcucumber seed germination.

Genetic linkage maps of Alstroemeria Brazilian species were constructed using AFLP markers. Reciprocal backcross mapping population with 122 individuals was obtained between A. inodora and A. psittacina, Brazilian species that are commonly used in the com