주방세제의 진딧물 살충효과와 분국화 생육에 미치는 영향 을 알아보기 위해 실험을 수행하였다. 복숭아혹진딧물과 목화 진딧물을 대상으로 주방세제 100, 200, 400배액 단용처리와 주방세제 400배액 100mL에 소주 10mL 또는 20mL를 혼용 하여 분무 처리하였다. 그 결과 주방세제 400배 이하의 모든 농도에서 복숭아혹진딧물은 85%, 목화진딧물은 90%의 살충 률을 보였다. 주방세제와 소주 혼용처리에 의한 살충효과 상 승은 보이지 않았다. 하우스안에서 진딧물이 많이 발생한 분 국화 잎에 400배액 이하의 농도로 3일 간격으로 2회 처리함 으로써 90% 이상의 진딧물이 감소되는 효과를 얻을 수 있었 다. 또한 분국화를 재배하면서 3~4일 간격으로 5주간 지속적 으로 주방세제를 처리했을 때, 대조구에서는 90% 잎에서 진 딧물이 발생한데 비해, 모든 주방세제 단독 처리구에서는 발 생율이 15% 이하로 낮게 유지되었다. 또한 국화의 생체중, 초 장, 엽수는 주방세제 농도가 높아질수록 조금씩 낮아지는 경 향이었으나, 초폭이나 분지수에서는 차이가 없었다. 그러나 주방세제 200배 이하의 농도에서는 국화의 잎이 갈변되거나 꽃잎 끝이 백화되는 약해가 관찰되었다.

이끼의 분쇄번식 시, 가장 적합한 배양토, 광, 온도를 구명 하기 위해 날개양털이끼(Brachythecium plumosum)와 쥐꼬리이끼(Myuroclada maximowiczii)를 이용하여 실험을 수행하였다. 실험 개시 4주 후에 사진을 찍어 Photoshop에서 이끼 면적과 녹색 평균값을 구하여 이끼의 생육 정도를 나타내었다. 배양토의 경우, 두 이끼 모두 다스란 상토에서 생육이 가장 좋았고, 상토:마사토(50:50), 원예상토, 마사토:피트모스(50:50) 에서는 비슷한 수준이었다. 버미큘라이트 단용에서는 생육이 부진하였다. 광도실험에서는 날개양털이끼는 25umol･m-2･s-1 에서 100umol･m-2･s-1까지 광도가 높아질수록 생육이 조금씩 좋아지는 경향이었으나, 쥐꼬리이끼는 3개의 광환경에서 비슷한 수준이었다. 온도 실험에서는 두 이끼 모두 23℃에서 면적과 녹색값이 가장 높아 생육도 좋았다. 이러한 결과를 종합 하면, 건조한 이끼를 분쇄하여 번식할 때, 배양토로는 보습력이 좋은 다스란 상토나 원예용 상토가 무난하며, 광도는 25~100umol･m-2･s-1 범위, 온도는 20~23℃가 적당할 것으로 판단된다.

현재 농가에서 이용되고 있는 보광등과 난방등의 특성을 조사하고 하우스내 기상 환경과 절화장미의 개화와 품질에 미치는 영향을 알아보기 위해 실험을 수행하였다. 보광등으로는 LED등(light emitting diode lamp, LED), 메탈할라이드등(metal halide lamp, MH), 고압나트륨등(high pressure sodium lamp, HPS)을, 난방등으로는 나노탄소섬유 적외선등(nano-carbon fiber infrared lamp, NCFI)을 절화장미 재배상 위에 설치하였다. 그 결과 LED와 NCFI의 광도는 각각 6.8μmol·m-2·s-1과 0.4μmol·m-2·s-1으로 매우 낮은 반면, MH와 HPS는 79 ~ 100μmol·m-2·s-1 범위로 높은 편이었다. 또한 LED와 MH는 적외선역에 파장이 없어 발열량이 거의 없었으나, HPS와 NCFI는 적외선역에 파장이 많아 발열이 많은 것으로 나타났다. 동일한 공간에서 칸막이로 실험구간을 나누어 실험이 수행되었음에도 불구하고 MH, HPS, NCFI에 의해 온도는 2°C 정도 상승되는 결과를 얻었으나, 습도에서는 처리간 차이가 보이지 않았다. 광도에 상관없이 모든 전등들은 절화장미의 개화를 촉진시켜 무처리구에 비해 적게는 5 ~ 7일, 많게는 12 ~ 14일 개화가 촉진되는 것으로 나타났다. 광량이 충분한 봄철에는 전조처리에 의해 개화소요일수가 짧아지는 만큼 절화장도 대조구보다 짧아졌지만, 광량이 부족한 겨울철에는 전조처리에 의해 절화장이 길어져 품질이 향상되는 결과를 얻을 수 있었다.

Chrysanthemums (Dendranthema grandiflorum ‘Iwanohakusen’) were grown in a greenhouse with complete nutrient solution system to investigate the effect of silicon (Si) supplement on salt induced deleterious effects in chrysanthemum plants. The experiment was conducted in plastic pots supplemented with a mixture of upland soil : leaf mold : river sand (3:3:4, v:v:v). Si and salinity were treated in combination with two levels of NaCl (0 and 100 mM) and two sources of silicon (K2SiO3, KSi and silicate fertilizer, SiF) at the same concentration (1.8 mM Si) by weekly-drenching for 12 weeks. Chrysanthemum plants supplemented with Si increased in fresh and dry matter enhancing water content and salinity tolerance. The plants grown under salt stress produced less fresh and dry matter than control plant. However, Si supplement to plants under salt stress ameliorated negative effects of salt stress. In soil, EC and NaCl increased by salt stress were mitigated by Si supplement. Salt stress significantly decreased the contents of K and P in leaf, but Si supplement under salt stress significantly recovered the decreased contents with enormous desorption of K and P in soil. Added Si significantly increased content of available SiO2 with its adsorption by salt stress in soil, which was directly related to Si accumulation in leaf. However, Si uptake by roots was suppressed by salt stress irrespective of Si supplement. Si supplement did not ameliorated the negative effects of salt stress on chlorophyll content and membrane integrity in leaf of chrysanthemum plant although significantly increased Si content in leaf, but reversed pest (Liriomyza trifolii) resistance to above-control level.

Epigenetic status of the genome of a donor nucleus has an important effect on the developmental potential of cloned embryos produced by somatic cell nuclear transfer (SCNT). In our previous study has results showed that the donor cells treated with 5-aza-2’- deoxyctidine (5-aza-dC, DNA methylation inhibitors) and Trichostatin A (TSA, histone deacetylase inhibitors) could improve the development of porcine nuclear transfer embryos in vitro. In this study we want to investigate why these two drugs treatment with the donor cell can improve the cloning efficiency, whether they can alter the epigenetic status of the genome of the donor nucleus. This study included 6 groups: control group, the donor cell (porcine fetal fibroblast cell) with no treatment; 2.5 nM 5-aza-dC group, the donor cells treated with 2.5 nM 5-aza-dC for 1h; 5-aza-dC group, the donor cells treated with 5 nM 5-aza-dC for 1h; TSA group, the donor cells treated with 50 nM TSA for 1h; 2.5 nM 5-aza-dC+TSA group, the donor cells treated with 2.5 nM 5-aza-dC for 1h and subsequently treated with 50 nM TSA for another 1h; 5-aza-dC+TSA group, the donor cells treated with 5 nM 5-aza-dC and 50 nM TSA together for 1h. The first experiment detected the DNA methylation status in the different groups. After treatment with these two drugs, the DNA methylation level of the donor cells decreased, however there is no significant difference among the groups. This result indicated that the donor cell treatment with 5-aza-dC and TSA can partially alter the DNA methylation status of the donor cells. The second experiment checked the histone acetylation level of the donor cells treated with these two drugs by western blot. TSA, 2.5 nM 5-aza-dC+TSA, 5 nM 5-aza-aC+TSA, these three groups can significantly improve the hisone acetylation level compared with control and 5-aza-dC groups, there is no significant difference among these three groups. The results of this study suggest that the donor cells treated with 5-aza-dC and TSA can partially decrease DNA methylation and can significantly improve the histone acetylation level of the donor cells, these alterations of the epigenetic modification maybe can improve the clonging efficiency.

5‐aza‐2’‐deoxyctidine (5‐aza‐dC) is DNA methylation inhibitor and Trichostatin A (TSA) is histone deacytlase inhibitor, both of them can alter the level of the epigenetic modification of cells. The objective of this study was to investigate the effects of treatment with 5‐aza‐dC and TSA into fetal fibroblasts on the development of porcine nuclear transfer (NT) embryos. In this study, experiments were performed in order to modify epigenetic status in donor cells and evaluate developmental potential of NT embryos. 5‐ aza‐dC or TSA or combining treatment of TSA and 5‐aza‐dC was treated into growing donor cells for 1 h exposure and development of NT embryos was evaluated. Experiment was performed with 3 groups: control group (donor cells without treatment); TSA group (donor cell treated with 50 nM TSA for 1 h); TSA + 5‐aza‐dC group (donor cells were treated with 50 nM TSA and 5 nM 5‐aza‐dC for 1 h); TSA+1/2(5‐aza‐dC) group (donor cells were treated with 50 nM TSA for 1h and subsequently treated with 2.5 nM 5‐aza‐dC for another 1h). When donor cells were individually treated with 5 nM 5‐aza‐dC or 50 nM TSA for 1h, the blastocyst rate of NT embryos increased significantly compared with control group [18.8% vs 13.4% (5 nM 5‐aza‐dC group vs control group), and 26.2% vs 11.8% (50 nM TSA group vs control group), p<0.05]. However, the blastocyst rate in combining treatment group (50 nM TSA + 5 nM 5‐aza‐dC) did not increase compare with control group (12.3% vs 11.8%, p>0.05). When the donor cell were individually treated with 50nM TSA for 1 h firstly and then treated with 2.5 nM 5‐aza‐dC for another 1h, the blastocyst rate was significantly improved compared with control and TSA group (28% vs 10.2% and 23.7%, p<0.05). The present study suggested that donor cells treated with TSA or low concentration of TSA+5‐azadC in short time exposure may enhance the development of porcine NT embryo.

For rapid production of freesia ‘Shiny Gold’ shoots by using a bioreactor, several culture conditions were investigated. Young shoots (< 1 ㎝) obtained from freesia corm section in vitro were used as plant materials for this experiment. As a basic experimental environment, 20 young shoots were inoculated into a 5 L balloon type bubble reactor which contained 1 L 1/2 strength MS medium supplemented with 30 g sucrose (3%), and the aeration was 0.1 vvm (vessel volumes per minute). The bioreactors were placed in a growth room with 23℃ temperature, 60% relative humidity and 60 μmol·m-2·s-1 light condition (16 h/8 h, day/night). The concentrations of MS media were set with 1/4, 1/2, 1 strength, medium volume 10, 20, 40%, sucrose concentration 3, 6, 9%, and aeration 0.1, 0.2, 0.4 vvm. After 4 weeks of cultivation, the growth indexes including the fresh and dry weight, and plant height were evaluated. At the same time, the consumption, pH, and EC of medium were estimated 4 weeks after incubating. The best results were achieved when 40 young shoots were incubated in a bioreactor in which 1 L of 1/2 strength MS medium supplemented with 6% sucrose was used for the rapid production of freesia shoots. The shoots were 17 cm in plant height and 1.0 g in fresh weight only 4 weeks after incubation which could be a good plant material suitable for corm enlargement i

‘Seohong’ was bred within the potato breeding program of National Institute of Highland Agriculture (NIHA). It was originated from a cross made in 1997 between ‘Jashim’ as a female and 93K65-1 as a male parent. Seohong was evaluated as a seedling number 97S05-1 for tuber characteristics, growth and yielding ability from 2001 to 2002, and than this clone was renamed as Daegwan 1-82. This clone was evaluated in the regional yield trial and the disease resistance in the five locations for three years. Finally, this clone was named as ‘Seohong’ and registered a new recommended potato cultivar in 2006. This cultivar has a round, shallow eye depth, light red-skinned tuber characteristics and low to medium dry matter content. It showed high resistance to common scab (Streptomyces scabies) and potato leaf roll virus (PLRV), however it was susceptible to potato virus Y (PVY) and late blight (Phytophthora infestans). Its mean tuber yields from the regional yield trial and winter cropping trial were 12 and 49 percent higher than that of ‘Superior’, respectively.

“Haryeong” was bred through the potato breeding program at the National Institute of Highland Agriculture (NIHA). Itin1996. It has a round, smooth, light yelow-skined tuber characteristics and high dry mater content. It showed high resistance tolate bligh

두께가 서로 다른 C3 식물의 잎은 단위엽면적당 광합성 능력에 있어서도 차이가 나는 바 잎의 내부구조와 기체교환 사이의 관계를 바탕으로 그 원인을 구명하였다. 광합성의 2대 제한요인으로 기체확산과 생화학적 과정의 상대적인 중요도를 결정하기 위해 중엽세포의 표면은 기체확산 저항의, 그리고 세포의 체적은 탄소고정 능력의 지표로 가정하였다. 즉 세포의 표면적이 증가하면 이산화탄소의 액상확산 저항이 감소하며 체적이 증대되면 carboxylation, oxygenation, 그리고 dark respiration 반응속도가 증가한다고 간주하였다. 이러한 개념을 함축하는 광합성 모형을 작성하고 이 가설의 검증을 위해 대두 품종 Amsoy잎을 이용한 실험을 수행하였다. 생장조절실내에서 200, 400, 600u mol photons m2 s1 PAR을 공급하여 서로 다른 두께의 잎을 준비하였으며 제3 및 4본엽에 대해 1,000 u mol photons m2 s1 PAR 및 28 기온 환경하에서 이산화탄소 흡수속도를 측정한 결과 세포의 체적과 표면적의 영향을 동시에 고려한 광합성 모형이 세포 표면적만을 고려한 경우 보다 실측치에 가까운 예측치를 산출하였다. 이로 미루어 세포의 표면적과 체적은 잎의 두께 및 그에 따른 광합성 능력의 예측에 적절한 변수로 간주된다.