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首页> 外文期刊>Scientia horticulturae >Effects of development, temperature, and calcium hypochlorite treatment on in vitro germinability of Phalaenopsis seeds.
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Effects of development, temperature, and calcium hypochlorite treatment on in vitro germinability of Phalaenopsis seeds.

机译:发育,温度和次氯酸钙处理对蝴蝶兰种子体外发芽能力的影响。

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There are no standardized procedures for sanitizing orchid seeds for propagation by tissue culture and there is insufficient information about the optimum stage of orchid seed development for best germination. Phalaenopsis amabilis flowers were hand-pollinated and fruits harvested 90, 105, and 120 d after pollination (DAP) for seed developmental analysis. Embryo cell number per seed was counted after staining with 4?-6-diamidino-2-phenylindole and viewing through a confocal microscope. Germination percentage and cell number per embryo increased from 14 to 61% and 41 to 66%, respectively, during fruit development from 90 to 120 DAP. Seeds from mature, browning (~140 DAP) Phalaenopsis Sogo Lit-Angel and Phalaenopsis spp. breeding line 9450 seed pods failed to germinate until frozen at -196, -80, or -18.C and thawed or chilled at 4.C for 10 d. Germinability in 140 DAP seeds was correlated with cracked testa after freezing and thawing. P. amabilis seeds were treated with 0, 5, 10, or 15% calcium hypochlorite (CH) for 5, 10, or 15 min. Ninety six percent of untreated seeds from 90 DAP fruit produced protocorms within 40 d after sowing (DAS). Exposing seeds to 5% CH for 10 or 15 min decreased germination to 85 and 73%, respectively. Exposure to 10 or 15% CH for 5, 10, or 15 min produced seed germination percentages of less than 40%. Protocorms developed root hairs and shoot primordia by 50 DAS and an average of one leaf and root by 85 DAS after treatment with either 0 or 5% CH. Higher concentrations delayed or inhibited protocorm development. Green fruits 120 DAP produced the highest percentage of protocorms, while ~140 DAP seeds from browning fruit were dormant but cold treatments increased germination.
机译:没有用于组织培养繁殖的兰花种子消毒的标准化程序,并且关于兰花种子发育的最佳阶段以获得最佳发芽的信息也不足。手工对蝴蝶兰花进行授粉,并在授粉后90、105和120天收获果实以进行种子发育分析。用4′-6-二dia基-2-苯基吲哚染色并通过共聚焦显微镜观察后,计数每个种子的胚细胞数。在果实发育从90到120 DAP期间,发芽率和每个胚的细胞数分别从14%增至61%和41%增至66%。成熟,褐变(〜140 DAP)蝴蝶兰Sogo亮天使和蝴蝶兰的种子。育种系9450的种子荚无法发芽,直到在-196,-80或-18.C冷冻并在4.C融化或冷藏10 d。冷冻和解冻后140份DAP种子的发芽性与破裂的睾丸相关。用0%,5%,10%或15%的次氯酸钙(CH)处理南美白对虾种子5分钟,10分钟或15分钟。 90个DAP果实中有96%的未处理种子在播种后40天内产生了原球茎(DAS)。将种子暴露于5%CH持续10或15分钟,其发芽率分别降至85%和73%。暴露于10%或15%CH中5、10或15分钟产生的种子发芽率小于40%。用0或5%CH处理后,原球茎通过50 DAS发育出根毛和茎原基,而通过85 DAS则平均形成了一片叶和根。较高的浓度会延迟或抑制原球茎的发育。绿色果实120 DAP产生的原球茎百分比最高,而褐变果实中约140 DAP种子处于休眠状态,但冷处理增加了发芽率。

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