• 한국산림과학회지
• /
• 제50권1호
• /
• pp.5-9
• /
• 1980

Polyacrylamide gel 전기영동법(電気泳動法)을 이용(利用)하여, 슬래쉬 소나무 (접목묘(接木苗), 20년생(年生))의 화아원기형성기간(花芽原基形成期間) 동안에 자화다량(雌花多量) 개화개체(開花個体)와 소량(少量) 개화개체간(開花個体間)에 정아(頂芽)의 peroxidase 동위효소(同位酵素)의 변화(変化)를 비교(比較)하였다. 정아(頂芽)에서 모두 9개의 band를 관측(観察)할 수 있었으며, 두 개체간(個体間)에 동위효소(同位酵素)의 양적(量的)인 차이(差異)는 미세(溦細)하였으나, 제오(第五) band는 다량(多量) 개화개체(開花個体)에서 대부분(大部分) 발견(発見)되었다. 제오(第五) band의 동위효소(同位酵素)는 자화원기형성(雌花原基形成)에 직접(直接) 관병(関聠)되는 것 같이 생각된다.

• 한국잡초학회지
• /
• 제17권2호
• /
• pp.207-213
• /
• 1997

단일식물인 수수의 개화에 지베렐린이 관여하는지를 조사하기 위하여 지베렐린 생합성 억제제인 ancymidol을 처리한후 내생 지베렐린의 함량과 개화 및 생육에 미치는 영향을 조사한 결과는 다음과 같다. 1. 지베렐린 생합성 억제제 ancymidol은 공시한 두 품종 모두의 생육을 억제함과 동시에 개화를 지연시켰다. 2. $GA_3$를 Ancymidol과 동시에 처리할 경우 생육억제와 개화지연이 모두 회복되어 지베렐린이 수수의 개화에 관여함을 보였다. 3. Ancymidol 10ppm은 수수의 모든 지베렐린 ($GA_{12}$, $GA_{53}$, $GA_{44}$, $GA_{19}$, $GA_{20}$, $GA_1$ 합성을 현저히 억제하였다.

• 원예과학기술지
• /
• 제31권6호
• /
• pp.726-731
• /
• 2013

저온암흑처리가 국내 육성 신품종 딸기의 화아분화에 미치는 영향을 구명하고자 실험을 수행하였다. 3월 29일에 모주를 정식하여 8월 2일에 런너를 절단하여 육성시킨 자묘를 7일간, 14일간, 그리고 21일간 $13^{\circ}C$ 저온저장고에서 저온암흑처리를 하였는데, 정식일인 2010년 9월 20일을 기준으로 역산하여 8월 21일에 3주간 처리, 9월 5일에 14일간 처리, 9월 12일에 7일간 처리를 각각 개시하였다. 처리 후에는 각각의 처리구별로 실체 현미경을 사용하여 형태적인 화아분화를 확인하였다. 또한, 저온암흑 처리한 딸기묘를 9월 20일에 고설수경재배 시스템에 일제히 정식하고 야마자키 조성딸기배양액을 EC $0.8dS{\cdot}m^{-1}$로 공급하여 재배하면서 처리별로 출뢰 및 개화를 조사하였다. 현미경으로 화아분화를 검경한 결과, 7일간의 저온암흑처리에서 '싼타'와 '매향'이 현저하게 빠른 화아분화를 나타내었다. 14일간의 처리구에서는 '설향'을 제외한 '싼타', '대왕', 그리고 '매향'은 현저하게 화아분화가 촉진되었다. 21일간의 처리구에서는 품종간에 유의성 있는 차이가 없었으며 다른 처리구에 비하여 화아분화의 진행이 늦었다. 정식 후의 개화율은 '설향'과 '매향'은 대조구인 무처리구와 큰 차이를 나타내지 않았다. 그러나, '싼타'와 '대왕'은 대조구에 비하여 현저하게 빠른 개화와 높은 개화율을 나타내어서 저온암흑처리 방법이 이들 두 품종에서는 조기수확 및 수량증대에 기여할 수 있는 기술로 기대된다.

• 한국작물학회지
• /
• 제46권6호
• /
• pp.478-482
• /
• 2001

콩의 생육단계별 야간조명 처리가 생리적 특성에 미치는 영을 분석하여 생육단계별 피해정도를 알아보고자 유한신육형인 신팔달콩 2호와 검정콩 1호, 무한신육형인 무한콩을 공시하여 유묘기, 화아분화 전기, 화아분화 후기, 개화기, 협 신장기 및 종실비대기의 6 시기의 야간에 각각 15일간씩 20~30 Lux(0.05~0.08W m$^{-2}$ , 0.24~0.36 $\mu$㏖ S$^{-1}$ m$^{-2}$ )의 조도에서 시험을 수행한 결과 요약하면 다음과 같다. 1. 개화기는 야간조명처리시 대조구에 비하여 2~8일 지연되었으며, 생육단계별로는 화아분화 전기에 야간조명시 7~9일이 지연되어 개화지연정도가 가장 컸다. 2. 경장은 대조구에 비하여 협신장기 이후 처리를 제외한 모든 처리에서 증가되었으며, 절수는 신팔달콩 2호 및 검정콩 1는 화아분화 추기 이전에 야간조명 처리시 증가되었으나, 무한콩은 화아분화 후기 이후 처리시 증가되었다. 3. 유한형 품종의 협수는 유묘기의 처리를 제외한 모든 처리에서 대조구에 비하여 감소되는 경향이었다. 4. 수량은 모든 생육단계의 야간조명 처리에서 감소되었으며, 감소 정도는 대조구에 비하여 화아분화 전기는 7~11%, 화아분화 후기에는 6~8%, 유묘기에는 5~8%, 개화기에는 3~8%이었다.

• 한국작물학회지
• /
• 제40권5호
• /
• pp.543-547
• /
• 1995

들깨잎의 주년생산을 위한 일장이 짧은 겨울동안 개화를 억제하기 위하여 들깨품종 엽실들깨, 옥동들깨에 대한 광조도별 0.5∼1 Lux, 3∼10 Lux, 30∼100 Lux, 야간조명시간별 10, 30, 60분간 처리로 실험을 수행한 결과를 요약하면 다음과 같다. 1. 엽실들깨는 옥동들깨보다 처리에 따라 정식후 개화소요일수는 1∼4일 정도 더 소요되었으며 광조도 0.5∼1Lux/야간조명시간 10분간 처리구 에서 개화소요일수가 가장 짧았으며 광조도 3∼10 Lux/야간조명시간 60분간 처리구와 광조도 30∼100Lux/야간조명시간 10, 30, 60분간 처리구 모두 개화가 되지 않았다. 2. 경장은 광조도 0.5∼1 Lux/야간조명시간 10분 처리구가 53∼56cm로 가장 작았고, 광조도 30∼100 Lux/야간조명시간 10분 처리구가 87∼91cm로 가장 컸다. 3.엽면적은 광조도 0.5∼1 Lux, 3∼10 Lux의 처리구에서는 야간조명시간이 길수록 광조도가 강할수록 엽면적은 증가되었으며 광조도 30∼100 Lux 처리구에서는 야간조명시간에 관계없이 엽면적은 큰 차이를 보이지 않았다. 4. 건물량은 광조도 30∼100 Lux/야간조명시간 10, 30, 60분간 처리구에서 주당 25∼29g으로 가장 무거웠고, 광조도 0.5∼1 Lux/야간조명시간 10분간 처리구에서 주당 16g으로 가장 낮았다. 5. 따라서 일장이 짧은 겨울동안의 개화억제 정도는 광조도 30∼100 Lux/ 야간조명시간 10분 정도 처리하면 효과가 커 그 이상 광조도와 야간조명시간은 엽생산을 위해 필요 없을 것으로 사료되었다.

• 한국자원식물학회지
• /
• 제7권1호
• /
• pp.63-66
• /
• 1994

The experiment was carried out to study the bothanical characteristics of Aconitum charmichaeli Sieb. et Zucc in Korea.The results obtained are summarized as follows ; maximum flowering date was 15 Sep. and plantheight was 65cm, stem diameter was 8.7mm, No. of node was 25 and node of flowering initiation was15th.In flowering, No. of anothers were 52 and No. of flowers were 49.In leaf, length and width was same size, lower leaf size was 2-3 times than upper leaf, lower leafarea was 8.4 times than upper leaf.In tuber, No. of tuber per plant was 8, fresh weight per tuber was 25.4g, total fresh weight per plantwas about 200g.

• 한국작물학회지
• /
• 제43권2호
• /
• pp.71-76
• /
• 1998

To define the relations between endogenous GA levels and growth and flowering in short-day plant sorghum, growth retardant BX-112 was applied to two sorghum genotypes, wild-type and phytochrome B mutant (phyB-1), which grows faster and flowers earlier than the wild-type. BX-112 and $GA_3$ were applied as a soil drench, and plant height, culm length, and date to floral initiation were investigated. Endogenous GAs contents were measured with GC-MS-SIM. BX-112 treatments inhibited shoot growth in both genotypes and drastically reduced $GA_1$ and $GA_8$ levels. With increasing BX-112 concentrations, $GA_1$ concentrations declined linearly, but caused the accumulation of intermediates from $GA_12$ to $GA_20$. This result implies that $GA_1$ is the major active endogenous GA in shoot elongation in a short day plant sorghum. The inhibition of plant growth in both of wild type and phyB-1 by BX-112 was very similar, while BX-112 effects on floral initiation in two types of plants differed significantly. Floral initiation of phyB-1 was not affected by BX-1l2, but that of wild-type was delayed as BX-1l2 concentration increased. Because BX-112 treatment causes accumulation of biosynthetic intermediates between synthetic pathway from $GA_12$ to $GA_20$ and because phyB-1 is altered in GA metabolism in this same region of the early C13-hydroxylation pathway, BX-112 may fail to block flowering of phyB-1.

• 한국자원식물학회지
• /
• 제31권6호
• /
• pp.591-596
• /
• 2018

This study was conducted to develop gibberellin treatment technique to enhance flower initiation in Aquilegia japonica Nakai & H. Hara. Seedlings were planted in 12cm-diameter pots on October 2016 and grown in green house. Ambient temperature in the green house was set at minimum $15^{\circ}C$ during day and night to suppress flower initiation at cold temperature condition. Two different types of gibberellin, $GA_3$ and $GA_{4+7}$, at 4 different concentration levels 100, 200, 400 and 600 mg/L, were tested in this study. Gibberellin was sprayed first at planting and secondly at 1-week after planting. Ten to fifteen ml of gibberellin was sprayed for each pot. Plant height and petiole length were elongated by both gibberellin types, flowering was more enhanced by $GA_3$ (91.7~100%) compared to of $GA_{4+7}$. However, abnormal flower was less observed in $GA_3$ treatment (0~16.7%) than $GA_{4+7}$. Number of flower stalks per plant ranged from 1.9 to 2.5. Number of flowers per plant ranged from 6.8 to 10.3. Differences in flowering characteristics between treatments were statistically significant. Optimal gibberellin treatment to enhance flower initiation in A. japonica Nakai & H. Hara substituting cold treatment was $GA_3$ at the concentration between 400 mg/L to 600 mg/L.

• 농업과학연구
• /
• 제40권4호
• /
• pp.297-303
• /
• 2013

This study was carried out to examine the effect of Red LED (660 nm) and fluorescent lamp for night break (NB) treatments of each 3 hours (22:30-01:30), 4 hours (22:00-02:00) and 5 hours (21:30-:02:30) per day for 53 days on flower bud initiation and growth in Chrysanthemum cv. 'Baekma' and cv. 'Jinba'. The days to flower budding after short-day treatment in 'Baekma' was longer at fluorescent lamp 4 hr (21.0 days) and 5 hr (20.5 days) NB, and it was shorter at Red LED 3 hr (14.2 days). The days to flowering after short-day treatment in 'Baekma' was longer at fluorescent lamp 4 hr (54.0 days), 5 hr (53.5 days) NB, and Red LED 5 hr (53.3 days), and it was shortest at Red LED 3 hr (50.2 days) NB treatment among all treatments. The days to flower budding after short-day treatment of 'Jinba' was longer at fluorescent lamp 4 hr (20.6 days) and was shorter at Red LED 3 hr (14.1 days) among all treatments. Similarly, the days to flowering after short-day treatment of 'Jinba' was longer at fluorescent lamp 4 hr (55.3 days) and was shortest at Red LED 3 hr (50.2 days) among all treatments. Therefore, inhibition of flower bud initiation was the most effective under fluorescent lamp 4 hr treatment. The length of cut flower of 'Baekma' was increased by fluorescent lamp 4 hr, 5 hr, and Red LED 5 hr, but of 'Jinba' was longer at LED 4 hr and 5 hr treatment. The weight of cut flower of 'Baekma' was heaviest at fluorescent lamp 5 hr treatment and was at Red LED 5hr treatment for 'Jinba' even though there was not statistically significant difference between 'Baekma' and 'Jinba'. Consequently, under fluorescent lamp 4 hr for night break was the most effective on flower bud initiation, flowering inhibition and cut-flower characteristics in 'Baekma' and 'Jinba'.

• 원예과학기술지
• /
• 제30권3호
• /
• pp.236-242
• /
• 2012

We investigated the influences of night interruption (NI) and night temperature on flowering and flower coloration in Cymbidium. Cymbidium 'Red Fire' and 'Yokihi' were grown under a 9 hours photoperiod (control), a 9 hours photoperiod with NI at a low light intensity (LNI) of 3-7 ${\mu}mol{\cdot}m^{-2}{\cdot}s^{-1}$, or a 9 hours photoperiod with NI at a high light intensity (HNI) of 120 ${\mu}mol{\cdot}m^{-2}{\cdot}s^{-1}$ for four hours (22:00-02:00 HR) for 16 weeks during the reproductive growth stage (Experiment 1). Thirty month-old Cymbidium 'Red Fire' plants with initiated flowering buds were placed in four different growth chamber with night temperature set points of 6, 9, 12, or $15^{\circ}C$ for 16 hours (18:00 to 09:00 HR) and a daytime temperature of $25^{\circ}C$ (Experiment 2). In Experiment 1, the numbers of visible buds and flowers increased, and time to flowering decreased in both the LNI and HNI treatments, as compared to the control in both cultivars. Red color in Cymbidium 'Red Fire' increased by both LNI and HNI, as evidenced by an increased $a^*$ in plants grown under these conditions, relative to those grown under the control condition. Number of days to visible buds at 9-$15^{\circ}C$ ranged from 31-34 days, as compared to 39 days at $6^{\circ}C$ in Experiment 2. Although as the temperature increased days to flowering decreased when the plant was grown at $15^{\circ}C$ as compared to 6, 9, or $12^{\circ}C$, the red color ($a^*$) also decreased. The number of flowers and percent flowering increased when the night temperature was maintained higher than $9^{\circ}C$. Therefore, NI treatment and maintaining the night temperature at approximately 9-$12^{\circ}C$ during the winter season after flower spike initiation in the reproductive developmental growth stage improve flower quality and controls flowering time.