We performed temperature dependent current-voltage (I-V) measurements to characterize the electrical properties of Au/Al2O3/n-Ge metal-insulator-semiconductor (MIS) diodes prepared with and without H2O prepulse treatment by atomic layer deposition (ALD). By considering the thickness of the Al2O3 interlayer, the barrier height for the treated sample was found to be 0.61 eV, similar to those of Au/n-Ge Schottky diodes. The thermionic emission (TE) model with barrier inhomogeneity explained the final state of the treated sample well. Compared to the untreated sample, the treated sample was found to have improved diode characteristics for both forward and reverse bias conditions. These results were associated with the reduction of charge trapping and interface states near the Ge/Al2O3 interface.

암반생물막의 군집구조와 생물량의 시, 공간적인 변화를 확인하기 위하여, 파도에 대한 노출이 다른 고사포와 격포에 서 11월부터 2011년 9월까지 격월로 암반조각을 채집하였다. 군집구조는 채집된 암반조각을 칫솔로 긁어 광학현미경 하에서 미세조류의 분류군별 개체수를 계수하여 분석하였고, 생물량은 NDVI, VI, 엽록소 a 농도를 측정하여 확인하였 다. 고사포와 격포의 조간대 암반생물막에서 가장 우점하는 분류군은 Aphanotece spp., Lyngbya spp.를 포함하는 남조류 였으며, 환경스트레스가 적은 조간대 하부에서는 규조류의 출현율이 높게 나타났다. 암반생물막에서 우점하는 규조류는 Navicula spp., Achnanthes spp.와 Licmophora spp.로 확인되었다. 식생지수와 엽록소 a 농도는 격포에 비해 고사포 생물막에서 높게 나타났다. 식생지수인 NDVI와 VI는 고사포에서 각각 0.49-0.40(평균 0.43), 2.64-3.22(평균 2.90)였으 며, 격포의 암반생물막은 NDVI와 VI가 각각 0.32-0.41(평균 0.38), 2.03-2.86(평균 2.48)으로 확인되었다. 엽록소 a의 농도는 고사포에서 12.79-32.87 ㎍/㎠(평균 22.84 ㎍/㎠)였고, 격포에서는 11.14-18.25 ㎍/㎠(평균 15.48 ㎍/㎠)로 식생지수와 마찬가지로 1월(겨울)에 최대, 3월(봄)에 최소인 계절 변화를 보였다. 엽록소 a 농도는 NDVI, VI와 양의 상관관계를 보여 비파괴적인 식생지수 측정방법이 파괴적인 엽록소 a 추출 방법을 대체할 수 있음을 알려준다. 결론적으 로 암반생물막은 여름보다 겨울에, 조간대 상부보다 중부와 하부에서, 파도에 보호된 해안보다 노출된 해안에서 높은 값을 보였다.

Even though plant protections using chemical pesticides have several advantages, non-specific toxicities to other beneficial insects and humans and rapid development of tolerance and/or resistance of target pests to chemicals are major disadvantages. Recent researches suggested that using double stranded RNA (dsRNA) could be species specific and environmental friendly pest management protocols. However, efficiency of dsRNA treatments are known to be variable according to its application methods. For example, injections of dsRNAs to pests were known to be effective in all species. However, efficiencies of oral application of dsRNAs were known to be dependent on species. Thus, development of tools that could enhance the efficacy of orally treated dsRNAs are utmost important for widening usages of dsRNAs in plant protection. Recently, we found that the efficacy of oral treated dsRNAs to target pests could be enhanced by nano-technologies. I will show how applying nano-technology to dsRNAs enhance the efficiency of dsRNAs. (This work was carried out with the support of the Cooperative Research Program for Agriculture Science & Technology Development (Project title: Studies for biological characteristics of and control methods against the migratory locust, Locusta migratoria, Project No: PJ011630042016), Rural Development Administration).

Freesia is one of the most popular flowers over the world including Korea, due to the fragrance and beauty of the plant flower. The first domestic freesia cultivar ‘Shiny Gold’ was developed by NIHHS, RDA, in 2003, which has yellow double and large petals and strong fragrance. Ten years have passed since ‘Shiny Gold’ was cultivated at floral farms, and the deterioration of cut flower quality and yield are reported from the farms. Virus infection causes a reduction in the quantity and quality of the cut freesia flowers and is one of the most serious problems in Korea. Virus detection was carried by reverse transcription polymer chain reaction (RT-PCR) for FreMV, FreSV, BYMV, CMV, and TRV, as known to infect freesia. FreMV, FreSV, BYMV, and TRV were detected single or multiply, and CMV was not found in the freesia leaves collected from the farms. To produce virus-free freesia, meristem culture of ‘Shiny Gold’ was conducted in MS medium added ribavirin at different concentration. As the increased of ribavirin concentration, the growth of ‘Shiny Gold’ plantlets was inhibited in freesia’Shiny Gold’. The plantlets produced by meristem culture in ‘Shiny Gold’ were virus free at the enzyme-linked immunosorbent assay (ELISA) level.