본 연구에서는 TCM-199, mSOF, NCSU-23 세 종류의 배지의 자연 단위 발생 유도로 형성된 돼지 배아의 초기 발육에 대한 효과를 조사하였다. 실험 1에서는 세 종류의 배지에서 체외 성숙된 도축장 유래 돼지 난자의 성숙율을 성숙 48 시간째 핵상 관찰로 조사하였다. 각 배지에서의 핵 성숙율은 mSOF군에서 83.12%, NCSU-23 군에서 78.03%, TCM-199군에서 83.52%로 세 배지의 난자 성숙율에 대한 유의적 차이는 없었다(P

An analysis of Lysiphlebus Foerster species reared from various field-collected aphid species determined the presence of probably trans-palearctic L. fabarum (Marsh.), L. testaceipes (Cress.) which is an accidentally introduced and established immigrant from North America, and L. koraiensis Stary sp. n., a native species of presumably broader distribution. Both parthenogenetic and biparental populations of L. fabarum were identified in Korea.

The suitable electric stimulation is essential for activation and fusion of oocytes before or after nuclear transplantation The present study was undertaken to determine the optirnal condition for the parthenogenetic activation of in vitro rnatured(IVM) bovine oocytes by electric stimulation. Different direct current(DC) electric voltage of 1.0, 1.5 and 2.0 kV/cm and pulse duration of 30, 60 and 120 sec were applied to the JVM nocytes in 0.3 M mannitol solution containing each 100 M CaCl and MgCl. IVM occytes at 24, 28 and 32 hours Post-maturation(hpm) were also electrically stimulated at 1.5 kV /cm, for 60 sec. The stimulated nocytes were then co-cultured in TCM-199 solution containing 10% fetal calf serum with bovine oviductal epithelial cells for 7~9 days in a 5% incubator at 39 ~ Their activation and in vitro development to morula and blastocyst were assessed under an inverted microscope. The higher activation rates 62.8 and 63.4% and in vitro de- velopment rates to morula and blastocyst 5.1 and 10.9% were shown in the oocytes stimulated at the voltage of 1.0 and 1.5 kV/cm than 2.0 kV/cm, respectively. No signifi- cantly(P<0.05) different activation rate was shown in JVM oocytes stimulated for 30, 60 and 120 sec, but developmental rates to morula and blastocyst was significantly(P<0.05) higher in the oocytes stimulated for 30 sec(6~3%) and 60 sec(10~0%) than 120 sec(0~ 0%). The aged oocytes at 28 and 30 hpm showed significantly(P<0.05) higher activation rates(72~7 and 79.7%) than the oocytes at 24 hpm(50~9%)~ Also, their developmental rates to morula and blastocyst were significantly(P<0.05) higher in the nocytes at 28(14.3%) and 32 hpm(15.9%) than 24 hpm(3.6%). From these results, it can be suggested that the optimal electric stimulation for IVM bovine occytes is a DC voltage between 1.0 and 1.5 kV/cm, pulse duration of 30 or 60 sec, and the optimal age of IVM oocytes for electric activation is at 32 hpm.