A Relationship between Length of Basis and Adventitious Root Formation in Pea Cuttings

A positive correlation between the length of the basis and the ability of the cuttings to form adventitious roots was observed in pea cuttings. Plants with a different basis length (the third internode) were obtained in different ways: Regulation by the level of irradiance, dark treatment or gibberellic acid. The length of the basis was also regulated by excision of the cuttings at different places on the stock plants. With increasing basis length an increase was found in the number of roots subsequently formed. The results were similar in cuttings from plants grown at different levels of irradiance or from dark treated plants. Optimal rooting was obtained by cutting the plants just above the second scale leaf. Cuttings from plants treated with 10^?3M GA₃ showed the same correlation between the length of the third internode and root formation as found in the other experiments, but the number of roots were at a lower level.     

Effects of auxin and irradiance on the rooting of cuttings of Pinus sylvestris

Abstract Seedlings of Pinus sylvestris L. were grown under controlled conditions (temperature 20°C, photoperiod 17 h) at two irradiances, 8 or 40 W m^-2. Hypocotyl cuttings were excised and rooted at different irradiances in tap water solutions of indolebutyric acid (IBA). The fastest rooting and highest rooting percentage were obtained with cuttings from stock plants grown at 8 W m^-2 and treated with 10^-5M IBA for 21 days. The concentration of 10^-4M IBA inhibited root formation. In comparable treatments rooting was always better in cuttings from stock plants grown at 8 W m^-2 than in cuttings from stock plants grown at 40 W m^-2. The irradiance during the rooting period had only a minor influence on rooting. When cuttings from plants irradiated with 40 W m^-2 were treated with 10^-5M IBA for 21 days the rooting percentage almost reached the same level as in untreated cuttings from stock plants given 8 W m^-2. In cuttings treated with IBA during the whole rooting period, rooting was depressed in comparison to untreated cuttings. Aeration of the 10^-4M IBA solution increased the rooting percentage, but aeration had no effect on untreated cuttings and on cuttings treated with lower IBA concentrations.     

Root Formation of Pea Cuttings in Relation to the Irradiance of the Stock Plants

Pea plants were grown at different irradiances for eleven days. At this stage they were used for cuttings. The irradiance during the rooting period (155 mW · dm^?2) was the same in all the experiments, Cuttings from stock plants cultivated at the weakest irradiance obtained the highest number of roots, and the poorest rooting appeared in cuttings from stock plants grown at the highest irradiance. The results indicate that the nutritional status of the stock plant is an important factor for root formation in the cutting. Light may influence the production of inhibitors which directly or indirectly affect root formation. The possible role of carbohydrates and growth promoters in the process of root formation is discussed.     

Influence of Cotyledon Excision and Sucrose on Root Formation in Pea Cuttings

Sucrose was supplied to stock plants of Pisum sativum L. cv. Alaska grown at different levels of irradiance. There was no significant effect on the rooting of the cuttings by sucrose supply to intact plants regardless of the irradiance. However, an increase in the number of roots per cutting was obtained at increasing concentrations of sucrose when the stock plants had been grown at 4 W m^?2 and their cotyledons had been removed two days before the cuttings were excised. Cotyledons were removed from stock plants at different times before the excision of cuttings with the intent to regulate the endogenous supply of carbohydrate. The number of roots per cutting was reduced by removal of the cotyledons and this reduction was correlated to the number of days the stock plants had grown without cotyledons as well as to the irradiance pre-treatment. A greater reduction occurred in cuttings from plants grown under 4 W m^?2 than from those grown under 38 W m^?2. The growth of the stock plants and the subsequent stem growth of the cuttings was determined by the irradiance to the stock plants and by the time of removal of the cotyledons. Exogenous supply of sucrose had no effect on the stem growth of the cuttings.     

Water stress and root formation in pea cuttings

The stock plants of pea (Pistum sativium L. cv. Alaska) grown for 11 days at 16 W m^?2 38 W m^?2 were subjected to different degrees of moisture stress, simulated with polyethyleneglycol (PEG, 6000) for different periods. The cuttings were made at the end of stress treatments, planted in perlite and allowed to root in a mist propagation chamber. The number of adventitious roots formed on the cuttings from non-stressed plants was significantly higher under low (16 W m^?2) than under high (38 W ^m?2) irradiance. However, under the influence of short duration stress the number of roots increased significantly under high but not under low irradiance. There was significantly poor rooting after prolonged stress under both irradiances. The leaf osmotic potential ψ_π showed a greater reduction with increasing degree and duration of stress at 38 W m^?2 than at 16 W m^?2. The differential rooting behaviour as a result of stress levels and irradiances is discussed in the light of available literature on adventitious root formation.     

Influence of the Irradiance on Carbohydrate Content and Rooting of Cuttings of Pine Seedlings (Pinus sylvestris L.)

Seedlings of Pinus sylvestris L. were grown for 6 weeks at an irradiance of either 8 or 40 watts per square meter in a controlled environment room. Cuttings from these plants were rooted in tap water for 75 days at either 8 or 40 watts per square meter. The photoperiod was 17 hours.

During the first 30 days of the rooting period quantitative changes in carbohydrates were recorded in cuttings from the different treatments. The carbohydrate contents of the cuttings were mainly regulated by the irradiance during the stock plant stage and generally a higher carbohydrate level was found in cuttings from stock plants grown at 40 watts per square meter.

The irradiance during the rooting period had only minor effects on the time course of root formation, whereas the irradiance during the stock plant stage did influence the subsequent root formation. Cuttings from stock plants grown at 8 watts per square meter rooted faster and with higher frequency than those from stock plants grown at 40 watts per square meter. These results are discussed in relation to the mentioned irradiance effects on carbohydrate content.

     

Morphactin and Adventitious Root Formation in Pea Cuttings

Stock plants of pea (Pisum sativum L. cv. Alaska) were grown at different controlled levels of irradiance (4, 16 or 38 W m^?2) for 11 days from sowing. Morphactin (CFM, methyl-2-chloro-9-hydroxy-fluorene-9-carboxylate) was applied to the apex of the stock plants 3 days before cuttings were excised. The cuttings were rooted at 16 W m^?2. High levels of morphactin (>5 × 10^?3 mg l^?1) inhibited root formation in the cuttings. Low concentrations of CFM (5 × 10^?5 mg l^?1) promoted the formation of adventitious roots in cuttings from plants grown at all three levels of irradiance, with the most pronounced effect in cuttings from 4 W m^?2. Measurements of ethylene evolution by CFM-treated plants 3 days after application, revealed a stimulatory effect on ethylene production by high CFM concentrations.     

Propagation of Hedera helix: Influence of irradiance to stock plants, length of internode and topophysis of cutting

Abstract Stock plants of Hedera helix cv. Pittsburgh were grown in controlled environment rooms at four different irradiances (light intensities) 10, 22, 37 or 46 W m^-2 PAR (photosynthetically active radiation). The root formation on single internode cuttings from these stock plants was observed in relation to length of the internodes and the position on the vine (topophysis). The analysis indicated that the root number was primarily dependent on internode length which in turn was dependent on irradiance to stock plants and topophysis. The irradiance of 37 W m^-2 PAR was optimal for internode length and root number and the basal internode was the one which produced the greatest number of roots.     

Quantification of IAA Metabolites in the Early Stages of Adventitious Rooting Might Be Predictive for Subsequent Differences in Rooting Response

Stock mother plants have gained importance in the process of adventitious rooting of woody plants in recent years. The present study reveals the role of the cutting position from a stock mother plant for subsequent rooting. Cuttings of Prunus subhirtella Miq. var. Autumnalis which originated from suckers at the bottom of a tree developed a rooting system of better quality (rooted cutting without callus formation, more main roots) compared to cuttings which originated from shoots at the top of a tree. The latter accumulated significantly more indole-3-acetic acid (IAA) with the highest value of 25.37 μg g^?1 FW on the severance date. These cuttings also contained more indole-3-acetyl-aspartate (IAA-Asp) on the second day after severance with the highest value of 4875.95 μg g^?1 FW compared to cuttings from the bottom-deriving suckers. The latter metabolised IAA primarily via 2-oxindole-3-acetic acid (oxIAA) and indole-3-methanol because the concentrations of these compounds increased at the base of these cuttings. The highest concentration of oxIAA, 8.3 mg ekv. IAA g^?1 FW, was measured 1 h after severance in cuttings from the bottom-derived suckers. With 590.5 ng ekv IAAg^?1 FW, the indole-3-methanol values were also significantly higher in the cuttings from the bottom shoots compared with cuttings from the top of the tree.     

Influence of the irradiance on phenols content and rooting of Ilex paraguariensis cuttings collected from adult plants

The influence of irradiance on phenolics contents and rooting of Ilex paraguariensis cuttings was studied. Results of the first experiment with stock plants under controlled-irradiance conditions show that when the irradiance level increased from 1.5 to 100 % PPFD, the oxidation of cuttings raised from 19 ± 11 to 88 ± 4 % (r ² = 0.64). At the same time, a strong correlation was observed between total phenolics content and irradiance (r ² = 0.7). In consequence, adventitious rooting diminished from 67 ± 5 to 3 ± 3 % under full radiation (r ² = 0.7). In the second experiment with stock plants subjected to field conditions, the results showed that the rooting process is strongly affected by the genotype (P < 0.0001), while the statistical analysis did not show a correlation between rooting and age of the donor plant. Season had a variable effect and depends on genotype. Although we did not find correlations between the rooting ability and the canopy structure of the stock plants, the position of the branches in the mother plant affected rooting and depended on season in addition to genotype. Concomitantly, the levels of soluble phenolics compounds were higher from leaves subjected to high-irradiance conditions than samples collected from inner canopy; which was coincident with the pattern of cuttings oxidation. In conclusion, our results provide evidences which support the hypothesis that the physiological status of the stock plant at the time that cuttings are excised is of utmost importance for the subsequent rooting of I. paraguariensis cuttings. The influence on soluble phenolics content of different irradiances given to the stock plants negatively affect the rooting process since the product of its oxidation cause the browning and death of the cuttings.     

Seasonal changes in adventitious root formation in hypocotyl cuttings of Pinus sylvestris: Influence of Photoperiod during stock plant growth and of indolebutyric acid treatment of cuttings

Seedlings of Pinus sylvestris were grown for 6 weeks under natural light conditions in a temperature controlled environment room. Cuttings from these plants were rooted in tap water or in indolebutyric acid (IBA) solutions for 60 days at an irradiance of 16 W m^-2. Experiments were performed at 3-week intervals during two growth seasons. — Seasonal changes in root formation were found in control cuttings as well as in IBA treated cuttings. The number of roots and the percentage of cuttings that rooted were high during early spring and autumn. During the summer period hardly any roots were formed. Stimulation of root formation by IBA occurred manily during spring and autumn when cuttings already possessed the ability to form roots. — The influence of photoperiod during stock plant growth was also investigated. Shorter photoperiod resulted in an increase in the number of roots and rooting percentage. The period during summer where rooting was inhibited under natural light conditions was considerably shortened when stock plants were grown at a photoperiod of only 4 h. The results demonstrate the importance of the growing conditions for stock plants for subsequent root formation. The results are discussed with special reference to the role of irradiance.     

Gibberellin A3 stimulates adventitious rooting of cuttings from cherry (Prunus avium)

We have examined the effect of exogenous gibberellin A₃(GA₃) on adventitious rooting of Prunus avium(cherry) cultivars Stella, F12/1 and Charger. We show that GA₃pre-treatment of P. avium stock plants causes an increasein shoot growth rate and also improves the rooting of cuttings subsequentlytaken from the treated plants. Approximately 37% of cuttings from controlshootsrooted, whereas the percentage rooting could be increased to 80% or more withGA₃ pre-treatment. The number of roots per rooted cutting was alsoincreased by GA₃ pre-treatment. The stimulation of adventitiousrooting could be partially explained by the increase in shoot growth rate.Cultivar Charger responded better than the other cultivars to the lowest levelof GA₃ treatment. In vitro cultures of cultivarCharger were also treated with GA₃. However, the stimulation ofadventitious rooting was less marked than in the GA₃-treated stockplants: percentage rooting increased from 70% to 85%. The results are discussedin the context of 'rejuvenation' effects of GA₃.     

Growth Performance of Cuttings Raised from in vitro and in vivo Propagated Stock Plants of Rosa damascena Mill.

Comparative studies on rooting and growth performance of cuttings raised from in vitro and in vivo grown plants of Rosa damascena are described. Cuttings were treated with different auxins and upon transfer to soil their growth performance was recorded. Overall, the auxin treated cuttings of in vitro raised plants responded better than the cuttings of in vivo raised plants. Optimal response for percentage of rooting, root number, root length and bottom breaks was observed at 100 mg dm^–3 IBA. The cuttings derived from in vitro raised plants showed a significantly better response for percent rooting, root number, root length and bottom buds in control treatments.     

Activity of Various Growth Substances in the Avena First Internode Test

The elongation growth of the Avena first internode segments was studied in the presence of one or several of the following growth substances: indoleacetic acid (IAA), 6-fur-furylamino purine (FAP, kinetin), 6-benzylamino purine (BAP), gibberellin A₃ (GA₃) and A₄₊₇ (GA₄₊₇), and abscisic acid (ABA). The cytokinins at concentrations of 10^?7 to 10^?6M stimulated growth with 4 to 6 per cent but this effect was not statistically significant. Concentrations higher than 5 × 10^?6M inhibited growth. FAP and BAP (from 10^?8M to 10^?6M) had no significant interaction with any other growth substance used. The two-factor interactions of IAA × ABA, IAA × GA₃, and GA₃× ABA, as well as the three-factor interaction IAA × ABA × GA₃ were significant. However, the IAA × ABA interaction was significant only when high concentration (10^?6M) of ABA was used. The growth inhibition produced by 10^?7 and 10^?6M ABA was overcome by about equimolar concentrations of IAA. The stimulation of growth by GA₃ and GA₄₊₇ (10^?9 to 10^?7M) was prevented by simultaneous application of ABA, and it was reduced significantly by application of IAA (10^?7 to 10^?8M). GA3 at 10^?8M combined with different concentrations of IAA gave slightly higher elongation than IAA alone but the observed values were significantly lower than expected assuming independent additive action.     

Conditions for rooting of leafy cuttings of Alnus incana

The rooting of softwood cuttings of Alnus incana (L.) Moench in nutrient solution was studied under controlled conditions. Cuttings consisting of one internode with the leaf and axillary bud attached rooted easily and more rapidly than shoot tip cuttings. Light was necessary for rooting but good rooting was obtained in photon flux densities of both 40 and 190 μmol m^-2s^-1. Root number and root length was reduced when light reached the base of the cuttings. Treatment with indolebutyric acid (10^-6–10^-4M) increased the number of roots but 10^-4M delayed rooting and decreased the root length. Debudded internode cuttings rooted as well as intact cuttings, and detached leaves also contained sufficient substances for rooting.     

Stock plant etiolation and stem banding effect on the auxin dose-response of rooting in stem cuttings of Carpinus betulus L. ‘Fastigiata’

Experiments were undertaken to determine the effect of stock plant etiolation and stem banding, prior to cutting propagation, on the auxin dose-response of rooting in Carpinus betulus L. Fastigiata stem cuttings. Stock plants were forced in a greenhouse, etiolated for 10 days and banded with black, light-tight Velcro for 8 weeks. Indole-3-butyric acid was applied to cuttings at concentrations ranging from 0 to 79 mM. Rooting percentages and numbers increased to a peak reponse at 20 mM in light-grown and 40 mM in etiolated shoots, followed by an inhibition at higher concentrations for all except etiolated and banded shoots. Cuttings prepared from shoots which had been etiolated or banded rooted better than controls at low and optimal IBA concentrations. Cuttings from shoots receiving both etiolation and banding also yielded higher rooting percentages and more roots per rooted cutting. Furthermore, etiolation and banding reduced the sensitivity of cuttings to supra-optimal auxin-induced inhibition of adventitious root initiation.     

Effects of Nutrients and Light on Growth and Root Formation in Pisum sativum Cuttings

Cuttings obtained from seedlings of Pisum sativum L. were rooted in water solution. Shoot growth continued after excision and shoot length increased considerably before roots emerged. Increase in dry weight was strongly dependent on light supply. Continued growth was dependent on supply of mineral nutrients to the rooting solution. Mineral nutrients had no or slight influence on the number of roots formed on cuttings from stock plants grown in fertilized soil, but the growth in length of the roots was dependent on the presence of calcium in the solution. Root formation was dependent on photosynthetic products formed after excision. No roots were formed on cuttings kept in the dark. The number of roots increased with increasing irradiance given to the leafy part of the cutting. At a low level of irradiance sucrose supply through the rooting medium increased the number of roots. Light given to the basal part of the cuttings had a strongly inhibitory effect on the number of roots formed. It is concluded that the carbohydrate level easily becomes a limiting factor for root formation in growing pea cuttings. Availability of mineral nutrients influences in the first place the growth of the shoots.     

Light effects on root formation in aspen and willow cuttings

The effect of light on rooting of leafy cuttings of aspen (Populus tremula × tremuloides) and a willow hybrid (Salix caprea × viminalis) was investigated under controlled conditions in water culture. Two levels of irradiance were used, 40 and 8 W m^?2. The lower level gave the best rooting of aspen cuttings, both when applied to the stock plants before the cuttings were taken and when given to the cuttings during the rooting period. Irradiation of the cutting base during the rooting period inhibited rooting almost completely in aspen and decreased the number of roots formed in the Salix hybrid. Net photosynthesis in the cuttings of Salix decreased considerably after excision and increased again after formation of roots. Indirect evidence indicated that photosynthesis was even more affected in aspen cuttings. The possible roles of carbohydrates and inhibitors in the light effects are discussed.     

Stimulation of putrescine biosynthesis via the ornithine decarboxylase pathway by gibberellic acid in the in vitro rooting of globe artichoke (Cynara scolymus)

Rooting and growth of globe artichoke (Cynarascolymus) cuttings were improved by supplementing the rooting mediumwith 10 M gibberellic acid(GA₃). Exogenous putrescine (Put) (0.5mM) raised the percentage of rooting to thesame level as GA₃, but decreased the number of roots per plant.Addition of Put to GA₃ produced the same effects on growthparametersand rooting percentage as Put alone. Changes in endogenous contents of freepolyamines (PAs) were determined in plants cultured 4 weeks in a rootingmedium.Whatever the treatments, rooting caused a large decrease in Put, the largelypredominant PA, in the leaves. GA₃ increased the free Put content ofthe leaves and roots. DL--difluoromethylarginine (DFMA), which inhibitsarginine decarboxylase (ADC), did not affect rooting while Put content wasdecreased by 12–15%. DFMA changed neither GA₃ effectsnor those from DFMO when used in combination. An inhibitor of ornithinedecarboxylase (ODC), DL--difluoromethylornithine (DFMO), inhibited leafgrowth as well as rooting and decreased the Put content; these effects werepartially reversed by addition of Put. GA₃ combined with DFMO didnotalleviate the inhibitory effects of DFMO. The GA₃ treatment caused aclear stimulation of ODC activity in the leaves; it also stimulated¹⁴C-putrescine uptake (2.8-fold) by leaves and its translocationtowards roots. These results indicate that the ODC pathway mediates thehormone-induced rooting response in globe artichoke. Moreover, a release of Putfrom its conjugates could contribute to the increase of free-Put levels in theroots under GA₃ treatment. Thus, Put can be considered to be a goodmarker of rhizogenesis.     

Non-Reversibility of Gibberellin-Induced Inhibition of Regeneration in Begonia Leaves

With applied to the petioles of detached Begonia x cheimantha leaves before planting, Gibberellic acid (GA₃) inhibited the formation of adventitious buds and roots ill an apparently irreversible manner. Bud formation was entirely suppressed by 10^?6M and higher concentrations and a significant inhibition was still present at 10^?9M the lowest concentration tested. Root formation was not affected by GA₃ below 10^?7M and was possible even at 10^?4 M GA₃. Petiole elongation was stimulated by GA₃ with an optimum at 10^?5M. GA₃ also blocked the action of 6-benzyiamino-purine (BAP) and 1-naphthaleneacetic acid (NAA), compounds which are potent stimulators of bud and root formation, respectively. When applied simultaneously with GA₃ they were, at their optimal concentrations, devoid of any effect in counteracting or reversing the gibberellin-induced inhibitions. Abscisic acid and the growth retardants CCC and Phosfon also were unable to restore bud and root formation. In leaves initially treated with water or 10^?5M BAP, endogenous bud and root formation as well as BAP-induced bud formation were entirety suppressed when 10^?5M GA₃ was applied 8 days after the initial treatments. Even when delayed for 14 days GA₃ treatment inhibited BAP-induced bud formation, while treatment after 21 days bad little effect on bud and root formation. Development of pre-existing, visible bud primordia was not inhibited by GA₃. BAP and NAA competitively inhibited the action of GA₃ in petiole extension growth. The results are discussed in relation to results obtained in other plant systems. It is suggested that GA₃ acts by blocking of the organized cell divisions initiating the formation of bud and root primordia.