玫瑰切花保鲜剂配方研究

以蔗糖(S)、8-羟基喹啉(8-HQ)、柠檬酸(CA)为保鲜液的基本配方,分别加入CaCl2 、NaCl、Al2(SO4)3、CaCl2+KAl(SO4)2 组成四种保鲜液,进行玫瑰切花保鲜实验。对切花瓶插寿命、花径、水分平衡值、可溶性蛋白含量和还原糖含量进行分析。结果表明,各种配方保鲜液均能延长玫瑰切花的瓶插寿命、增大花径、改善切花水分代谢状况、降低切花蛋白质和还原糖的分解速度。其中,保鲜液2% S + 280 mg/L CA + 200 mg/L 8-HQ + 1% CaCl2的保鲜效果最好。     

表面活性剂对香石竹切花保鲜效果的研究

目的:解决香石竹采后运输和瓶插过程中花朵衰老问题.方法:研究表面活性剂对香石竹切花保鲜效果,测定瓶插期间的花枝鲜重、花朵直径、SOD活性.结果:由蔗糖25mg/L+柠檬酸200mg/L+8-HQ 200mg/L+吐温0.01%组成的保鲜剂配方,比对照能延长切花瓶插寿命11.4d.结论:在保鲜剂配方中可以使用表面活性剂(如吐温)等物质,其浓度控制在0.01%范围内.     

保鲜剂对晚香玉切花的保鲜效应

以晚香玉切花为材料,用蔗糖、6-BA、8-HQC和酒石酸按四因素三水平的正交设计配制保鲜液,通过测定瓶插寿命、小花开放率、鲜重、可溶性糖和电导率,研究不同保鲜剂的保鲜效果。结果表明：与对照相比,各处理均能不同程度地延缓切花衰老,其中处理9即12g.L^-1蔗糖＋60mg·L^-16-BA＋400mg·L^-18-HQC＋100mg·L^-1酒石酸效果最好,花枝瓶插寿命比对照长6d,70％的小花开放,其他指标均明显优于对照,是晚香玉切花较好的保鲜配方。     

不同保鲜剂对非洲菊切花的保鲜效应

探讨不同保鲜剂对非洲菊切花的瓶插寿命、观赏品质以及生理生化指标的影响。结果表明,在供试7组保鲜剂中,以处理7(T₇):20g/L Suc+200mg/L 8-HQC+150mg/L CA+75 mg/L KH₂PO₄·3H₂O+1g/L CaCl₂的保鲜效果最佳,可显著延长非洲菊切花瓶插寿命;T₇处理有利于减缓花瓣组织pH上升、花青素含量下降及花瓣细胞膜相对透性的上升,从而延长瓶插寿命。     

四种鲜切花保鲜剂的筛选

本文研究了四种鲜切花(唐菖蒲、月季、康乃馨和鹤望兰)的保鲜剂配方,观测各种保鲜剂对切花外观品质和瓶插寿命的影响,从中筛选出各种鲜切花的较佳保鲜剂,并讨论了组成保鲜剂配方的各种成分(糖、杀菌剂、有机酸、无机盐、乙烯抑制剂和拮抗剂以及植物生长调节剂)的作用。     

不同保鲜剂对月季切花的保鲜效应

本试验研究不同保鲜剂对月季切花瓶插寿命、观赏品质的影响。正交试验表明,在供试保鲜剂的9个组合中,配方7(P₇)[0.2% Ca(NO₃)₂+0 Suc+400mg/L B₉+1mmol/L STS]保鲜效果最好,可明显延长月季切花瓶插寿命;以P₇保鲜剂喷洒花瓣可促进花朵生长发育;月季切花在瓶插过程中,其花瓣组织的pH值随切花的衰老而上升。     

不同保鲜剂对香石竹切花的保鲜效果

3种保鲜剂均能不同程度地增加切花鲜重,增大花径,改善切花体内的水分状况,降低过氧化物酶(POD)活性,延长瓶插寿命,其中以保鲜剂3(40mg·L~(-1)苯甲酸+50mg·L~(-1)AgNO_3+3％蔗糖+200mg·L~(-1)8-HQ)的保鲜效果最好。     

小苍兰切花不完全开放的原因探讨及防止措施

本文探明了小苍兰切花瓶插过程中小花不完全开放的原因,是由于采收时切花体内自身糖分积累不足所致。用高浓度(10%,20%,30%)蔗糖液处理,可增加切花各主、侧花序含糖量,提高开放率并延长瓶插寿命。同时还研究了几种含糖、化学药剂及激素的瓶插液对小花开放、花色和瓶插寿命的效应,以S+8-HQC+KT(蔗糖+8-羟基喹啉柠檬酸盐+激动素)效果较佳。此外,还比较了糖液处理和化学药剂保鲜两种方法的利弊和应用范围。     

保鲜剂及冷藏对鹤望兰切花瓶插品质的影响

本文探讨不同保鲜剂、预处理液及冷藏时间对鹤望兰切花瓶插寿命和观赏品质的影响。结果表明,供试的8组瓶插保鲜液中,以配方5% S+300 mg/L 8-HQC+100 mg/L CA+150 mg/L STS+100 mg/L CoCl₂+25 mg/L EDTA-Na保鲜效果最佳,切花瓶插寿命(23.5 d)比CK延长15.2 d,小花开放率(56.1%)比CK提高1.19倍。供试的5组冷藏预处理液中,以10% S+300 mg/L 8-HQC+75 mg/L KH₂PO₄·3H₂O效果最佳,切花经过2~3周8~10℃冷藏后,瓶插寿命(13.7 d)比CK延长7.9 d,小花开放率(43.6%)比CK提高98.2%;该处理组鹤望兰切花的适宜冷藏时间可延长为3周。     

满天星切花保鲜技术研究

本实验对化学药剂处理后满天星切花在瓶插期间的寿命、品质、PH值等进行了研究.结果表明,本实验所用的保鲜剂对满天星切花具有较好的保鲜效果.可生长其瓶插寿命3—5天,且能提高观赏品质和开花率;经保鲜剂处理后,切花显著增重;随着瓶插时间的延长,PH值有增大的趋;结合包装、致冷剂等其它处理,可使满天星切花保鲜10天左右.     

烯效唑（S-3307）对非洲菊切花保鲜的影响

以非洲菊(GerberajamesoniiBolus)切花为材料,以保鲜基本液(BP,20gL-1蔗糖 200mgL-1柠檬酸 150mgL-18-羟基喹啉柠檬酸盐)和添加30mgL-1烯效唑(S-3307)的基本液(BP S-3307)作对比实验,通过对切花外部形态观察和切花衰老过程中一些生理生化指标测定,探讨了S-3307对非洲菊切花的保鲜效果。结果表明,S-3307处理使切花的瓶插寿命比对照(蒸馏水)延长了4.3d,比BP处理延长了2.3d,而弯颈率分别仅为对照和BP处理的9.6%和28.8%。说明S-3307可增强切花的吸水能力,增加花枝的鲜重,延缓了切花花瓣中蛋白质的降解和抗氧化酶SOD和CAT活性的下降,并减少了游离脯氨酸和MDA的积累,维持膜结构的相对稳定性,从而延缓了非洲菊切花的衰老和提高了切花瓶插期间的观赏品质。     

保鲜剂对夏季香石竹切花衰老的延缓作用

香石竹切花瓶插期间花瓣中ＳＯＤ和蛋白质在前期上升,然后比处理组提前３天呈下降趋势。采后花瓣中ＣＡＴ、可溶性总糖和蔗糖均为下降。经由蔗糖、８－羟基喹啉和植物生长调节剂或钴镍盐组成的保鲜剂能延缓切花花瓣中ＳＯＤ、ＣＡＴ活性的下降,阻碍蛋白质、可溶性总糖和蔗糖的降解速度,同时使切花的瓶插寿命延长、含水量增加。     

植酸对月季切花瓶插寿命的影响

用0.13％和0.013％植酸对月季切花进行处理,探讨了植酸对月季切花瓶插寿命及衰老过程中一些生理生化指标的影响.结果表明,013％和0.013％植酸处理的切花,瓶插寿命分别延长了2.3 d和1.4d.植酸处理抑制了O-2含量的增加和POD活性的提高,从而减轻了O-2对植物细胞的伤害即抑制丙二醛含量增加,同时抑制了可溶...     

Evaluation of several holding solutions for prolonging vase-life and keeping quality of cut sweet pea flowers (Lathyrus odoratus L.)

Cut spikes of sweet pea (Lathyrus odoratus L.) were kept in 2% sucrose, 200 ppm 8-hydroxyquinoline sulfate (8-HQS), pulsing treatment with 200 ppm 8-HQS in combination with 2% sucrose for 12 h, pulsing the spikes with 0.2 mM silver thiosulfate (STS) for 1 h and pulsing with 0.2 mM STS for 1 h followed by 2% sucrose solution. Therefore, this study aimed to see their effects on keeping quality and vase-life of the cut flowers. A control (deionized water) and a standard preservative were also included in the experiment. The results showed that all treatments had improved the keeping quality and vase-life of the cut flowers comparing to control ones. Among all these treatments, the 8-HQS combined with 2% sucrose showed the best water uptake, water balance, percentage of maximum increase in fresh weight of the cut flower stems and vase-life which was extended up to 17 days. Moreover, this keeping solution retarded the chlorophyll as well as carbohydrate degradation. However, anthocyanin concentrations were increased by treatments with sucrose alone or STS followed by sucrose during the postharvest life. It has been concluded that 200 ppm 8-HQS combined with 2% sucrose solution has the potential to be used as a commercial cut flower preservative solution to delay flower senescence, enhance post harvest quality and prolong the vase-life of sweet pea cut flowers.     

Effects of postharvest pretreatments and preservative solutions on vase life longevity and flower quality of sweet pea (Lathyrus odoratus L.)

The effects of postharvest pretreatments on vase life, keeping quality and carbohydrate concentrations in cut sweet pea (Lathyrus odoratus L.) flowers were investigated. Compared to the control, all treatments promoted floret quality and extended longevity. The cut flowers held in the solution containing sucrose + 8-hydroxyquinoline (Suc+HQS) was more effective in promoting absorption rate, achieved greater maximum fresh mass, had better water balance for a longer period, extended the vase life (up to 17 d), and delayed degradation of chlorophylls. The same treatment also enhanced the concentration of soluble carbohydrates in the petals and stems and leaf chlorophyll (Chl) content, whereas it was lowest in silver thiosulphate (STS) treatment. However, concentrations of anthocyanin in the petals were higher for treatment with sucrose or STS plus sucrose than in control or STS alone treatments. Our results suggest that pulse treatment with HQS plus sucrose for 12 h is the most effective for improving pigmentation and use as a commercial cut flower preservative solution to delay flower senescence, enhance quality, and prolong the vase life of sweet pea. The results also showed that soluble carbohydrate concentration in petals and stems is an important factor in determining the vase life of sweet pea flowers.     

Translocation of 14C-sucrose in Relation to Changes in Carbohydrate Content in Rose Corollas Cut at Different Stages of Development

The dry matter and carbohydrate contents of intact growing ‘Sonia’rose corollas were measured from an immature bud to full expansionof the petals. Reducing sugars and starch, but not sucrose,accumulated throughout most of the corolla development. Thesefindings were compared with the carbohydrate changes in thecorollas of flowers cut at different stages and allowed to agewith their stems either in water or in a sucrose-containingsolution. For a few days after cutting the carbohydrate metabolismof the cut flower roughly paralleled that of the intact floweruntil starch hydrolysed to maintain the soluble carbohydratepool. Feeding with the sucrose solution maintained the solublecarbohydrate levels and retarded the hydrolysis of starch. The cut flowers were fed with ¹⁴C-sucrose and the labelled metabolitesin the leaves and flowers were analysed. Active incorporationof ¹⁴C into ethanol-soluble carbohydrates, starch and ethanol-insolublematerial was found indicating that an active anabolic phaseprecedes the catabolic phase during the senescence of the cutflower. The findings are discussed in relation to the source-sinkhypothesis of flower development, with regard to the senescenceand growth of the corollas of cut and intact flowers respectively.     

Invertase and sucrose synthase in flowers

Sucrose and reducing sugar concentrations in petals of cut carnation flowers, whose life was prolonged up to 7 days by bathing stalks in sucrose solutions, were respectively 3-fold and 2-fold higher than those bathed in water. Reducing sugar concentrations were about 7-fold higher than sucrose concentrations. A study of invertase and sucrose synthase activities in flower petals of carnation and four other species of flowers revealed that both enzymes may be involved in hydrolysis of translocated sucrose. Invertase activity, while being up to 20-fold higher than sucrose synthase activity in some species was approximately comparable in others. More detailed studies on invertase from petals of 3 flower species demonstrated the presence of only the acid form of the enzyme with a K_m value for sucrose of about 2.5 mM.     

表油菜素内酯对月季切花保鲜作用的研究

本文初步探讨了表油菜素内酯（epiBR）对瓶插月季切花的保鲜作用。与对照（蒸馏水）和基本液（2％蔗糖＋500mgL-1柠檬酸＋250mgL-8-羟基喹啉＋25mgAgNO3）相比,经epiBR处理（基本液＋0．1mgL-1epiBR）的月季切花花枝坚挺,蓝变延迟,瓶插寿命延长1-1.5倍。测定有关生理指标表明,epiBR处理对月季切花瓶插花枝前期鲜重的增加及后期的保持有明显作用。并显著延缓花瓣和叶片质膜相对透性的增加,还能使瓶插前期花瓣还原糖含量增加。epiBR处理对花瓣蛋白质和叶片叶绿素含量变化无明显影响,而对花瓣花青素水平下降有轻微的促进作用。     

Effects of Sucrose on Water Relations of Cut, Senescing, Carnation Flowers

Carnation flower stems were stood in water or sucrose solutionand changes in water content, water and osmotic potential, turgorpressure and solutes (sugars, nitrogen, phosphorus, potassium)of petals were measured throughout the flower life. In bothtreatments the petals had a higher specific water content atincipient wilting than when the flowers were first cut. In water,turgor pressure decreased rapidly after the seventh day becauseof a decrease in tissue solute content. In sucrose solution,loss, of solutes was delayed probably because the sugar provideda respiratory substrate to maintain cell membrane integrity.In these cells, sugars and water accumulated causing decreasesin water potential and osmotic potential. Solutes and waterwere lost at about day 15 and turgor pressure decreased. Therewas some evidence that from about day 11 cells were so gorgedwith sugars that they burst when they were placed in water duringthe adjustment of water content prior to water potential measurements. Most of the initial petal osmotic energy content could be accountedfor by sugar, potassium, and anions associated with potassium,but in water, as the petals aged and sugar content decreased,so the potassium ions contributed a larger proportion of theosmotic energy; with stems in sucrose, the endogenous sugarcontent (reducing sugars plus sucrose) contributed an increasingproportion of the total osmotic energy. Dianthus caryophyllus, carnation, flowers, water relations, senescence     

Production of essential oils by flowers of Hyacinthus orientalis L. regenerated in vitro

Essential oils were produced by flowers of Hyacinthus orientalis L. that had been regenerated in vitro. The production of these oils was affected by the concentration of gibberellic acid and sucrose in the medium and by temperature. The highest concentration of essential oils was obtained when regenerated flowers were cultured in vitro for 3 weeks at 20 °C on Murashige and Skoog's medium that contained 30 g/l sucrose plus 1 mg/l gibberellic acid, whereas the highest amount of essential oils was obtained after a culture period of 3 weeks at 25 °C. The composition of essential oils from flowers that had been regenerated in vitro was compared with that from flowers grown in the field. Essential oils detected by gas-liquid chromatography included nine components in the case of the regenerated flowers and six and ten components in the case of stage 3 and stage 4 flowers grown in the field, respectively. There were four common components, namely, 1-hepten-3-ol, benzyl alcohol, phenethyl alcohol and cinnamyl alcohol. In the regenerated flowers, a single component, phenethyl alcohol, was a major constituent (75%), whereas two compounds, phenethyl alcohol (stage 3, 55%; stage 4, 48%) and cinnamyl alcohol (stage 3, 23%; stage 4, 29%) were the major constituents in the case of flowers grown in the field. Four and five other components were specific to flowers regenerated in vitro and field-grown flowers, respectively.Abbreviations BA 6-benzylaminopurine - 2,4-D 2,4-dichlorophenoxyacetic acid - IAA indole-3-acetic acid - NAA 1-naphthaleneacetic acid - ABA abscisic acid - GA₃ gibberellic acid - ACC 1-aminocyclopropane-1-carboxylic acid - ethephon (2-chloroethyl)phosphonic acid - MS medium Murashige and Skoog's medium - GLC gas-liquid chromatography - GC-MS gas chromatography-mass spectrometry - FW fresh weight