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  • Author or Editor: Jianjun Chen x
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Chlorophytum amaniense Engl. ‘Fire Flash’ is a popular exotic ornamental foliage plant as a result of its unique coral-colored midribs and petioles and tolerance to interior low light levels. Currently, demand for propagative materials exceeds the availability of seeds. This study was intended to develop an in vitro culture method for rapid propagation of this cultivar. Leaf and sprouted seed explants were cultured on a Murashige and Skoog basal medium supplemented with different cytokinins with 1.1 μM α-naphthalene acetic acid (NAA) or 2.3 μM 2,4-dichlorophenoxyacetic acid (2,4-D). Leaf explants showed poor responses in callus production and no adventitious shoots were obtained. Callus formation frequencies from sprouted seeds were 71% and 85% when induced by 9.8 μM N6-(2-isopentyl) adenine (2iP) with 1.1 μM NAA and 9.1 μM N-phenyl-N′-1,2,3-thiadiazol-5-ylurea (TDZ) with 1.1 μM NAA, respectively. Adventitious shoots occurred after the induced calluses were subcultured on the same concentrations of TDZ or 2iP with NAA. Shoot formation frequencies from calluses cultured on TDZ with NAA and 2iP with NAA were 92% and 85%, and the corresponding mean shoot numbers were 37 and 31 per piece of callus (1 cm3), respectively. Adventitious shoots rooted at 100% after transferring to the basal medium containing 4.4 μM 6-benzylaminopurine (BA) with 2.7 μM NAA. Plantlets, after transplanting to a soilless substrate were easily acclimatized in a shaded greenhouse under a photosynthetic photon flux (PPF) density of 200 μmol·m−2·s−1. Regenerated plants grew vigorously without undesirable basal branching or distorted leaves. This newly established regeneration method can provide the foliage plant industry with a means for rapidly propagating ‘Fire Flash’ liners in a year-round fashion.

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This study established a method of regenerating Dracaena surculosa Lindl. ‘Florida Beauty’ through indirect shoot organogenesis. Bud, leaf, and stem explants were cultured on a Murashige and Skoog basal medium supplemented with N6-(2-isopentyl) adenine (2iP) at 12.3 and 24.6 μM with 3-indoleacetic acid (IAA) at 0, 1.1, and 2.3 μM, respectively, and 2iP at 36.9, 49.2, 61.5, and 73.8 μM with IAA at 1.1 and 2.3 μM, respectively. Calluses were induced from leaf explants but failed to produce adventitious shoots. Calluses were also induced from stem and bud explants cultured on the basal medium containing 12.3 μM 2iP and 2.3 μM IAA, 24.6 μM 2iP or higher with either 1.1 or 2.3 μM IAA. The highest callus induction frequency was 63.2% from stem explants and 69.6% from bud explants when they were cultured on the basal medium supplemented with 49.2 μM 2iP and 2.3 μM IAA. The highest shoot formation frequency was 65.7% from stem-derived callus cultured on the basal medium containing 61.5 μM 2iP and 1.1 μM IAA and 88% from bud-derived callus cultured with 49.2 μM 2iP and 1.1 μM IAA. The highest number of shoots per piece of stem- and bud-derived calluses was 3.8 and 6.7, respectively. Adventitious shoots developed better root systems in the basal medium supplemented with 2.0 μM IAA. Plantlets after transplantation into a soilless substrate grew vigorously in a shaded greenhouse under a maximum photosynthetic photon flux density of 300 μmol·m−2·s−1. Neither disease incidence nor somaclonal variants were observed in the regenerated population. This established method could be used for efficient micropropagation of D. surculosa, and the availability of tissue-cultured liners could reduce the dependency on imported cuttings, which often bring new or invasive pests into the United States.

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Gynura aurantiaca is a colorful foliage plant with creeping stems and velvety purple hairs that cover the green leaves. It grows rapidly, but is cultivated primarily for those attractive purple leaves. Annually during the spring, this plant produces prominent flowers both in appearance and smell, gaudy and malodorous. Flowering coupled with acquiring an over-grown leggy appearance have been key limitations in its production and use in interiorscaping. This study was undertaken to determine if an available commercial plant growth regulator could inhibit flowering. A-Rest (ancymidol), B-Nine (daminozide), Bonzi (paclobutrazol), cycocel (chlormequat chloride) and florel (ethephon) each diluted to three different concentrations were sprayed in two applications in early spring at 2-week intervals. Flowering and bud numbers and plant growth (number of lateral shoots, vine lengths and internode lengths) were recorded. Results indicated that applications of A-Rest, B-Nine, Bonzi and Cycocel, regardless of treatment concentrations, were ineffective in suppressing the flowering of this plant; whereas, florel completely suppressed flowering at the three concentrations used. The florel-treated plants also grew more lateral shoots, which produced a compact and dense bush-look, indicating that appropriate concentrations of florel application not only will stop flowering of purple passion but can also improve and prolong its aesthetic value as a potted or hanging-basket interior plant.

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Silicon (Si) is the second most-abundant element in soils, and its concentration in soil solution ranges from 0.1 to 0.6 mm, which is the same concentration range as some of the major nutrient elements such as calcium, magnesium, phosphorus, and sulfur. Increasing evidence has recently suggested that Si plays important roles in improving plant growth. However, little information is available on Si effects on container-grown ornamental plants, particularly since most are grown in soilless media where Si sources are greatly limited. The objectives of this research were to evaluate Si absorption and translocation in diverse container-grown ornamental plants and to determine whether Si absorption could improve plant growth. Liners from 39 plant species were potted in peat and pine bark-based soilless media and grown in a shaded greenhouse. Plants were fertigated with a Peter's 24–8–16 water-soluble fertilizer containing 0, 50, and 100 mg·L–1 of Si. Once marketable sizes were reached, plants were harvested and fresh and dry weights determined; Si and other nutrient elements in roots and shoots were measured. Results indicated that 32 of the 39 evaluated species were able to absorb Si, with large quantities further transported to shoots. Of the 32 Si-responsive species, 17 showed significant dry weight increases, whereas the other 15 only exhibited Si absorption and translocation with no apparent growth responses. The seven non-responsive plant species showed no significant increases in neither Si absorption and translocation, nor dry weight.

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Calathea, the largest genus in the family Marantaceae, is composed of 100 species native to tropical America in moist or swampy forest habitats. Because of their brilliant patterns of leaf color and different textures plus ability to tolerate low light levels, calatheas have been widely produced as ornamental foliage plants for interiorscaping. Thus far, genetic relationships among its species and cultivars have not been documented. This study analyzed the relationships of 34 cultivars across 14 species using amplified fragment length polymorphism (AFLP) markers. Six EcoR I + 2/Mse I + 3 primer set combinations were used in this investigation. Each selected primer set generated 105 to 136 scorable fragments. A total of 733 AFLP fragments were detected of which 497 were polymorphic (68%). A dendrogram was constructed using the unweighted pair-group method of arithmetic averages (UP-GMA) technique and a principal coordinated analysis (PCOA) was used to analyze the relationships. The 34 cultivars were divided into four clusters. Cluster I had 19 cultivars derived from C. roseo-picta and C. loesnerii with Jaccard's similarity coefficients from 0.74 to 0.97, of which six are somaclonal variants or sports and two cultivars are genetic identical. Only C. kennedeae `Helen' is positioned in cluster II. Cluster III had 10 cultivars across seven species; Jaccard's similarity coefficients among them varied from 0.41 to 0.63. Four species were situated in cluster IV with Jaccard's similarity between 0.27 to 0.41. Results from this study indicate that broadening of genetic diversity is needed for cultivars in cluster I as they are the most commonly grown calatheas but genetically are very close.

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The irritant effect of Dieffenbachia sap is attributed to protelytic enxymes but calcium oxalate crystals are considered to puncture cells and allow enzyme entrance. To date, no detailed study of the location, type, or frequency of calcium oxalate crystals in Dieffenbachia species or cultivars has been undertaken. To do so, three uniform tissue culture plantlets of Dieffenbachia `Carina',`Rebecca' or `Star Bright' were transpanted into 15 cm pots, grown in a shaded greenhouse under 385 μmol·m-2·s-1 and fertigated with 20 N-8.7 P-16.6 K water-soluble fertilizer at N concentrations of 200 mg·L-1 twice weekly. Ten weeks later, samples of stem, root, and leaves were taken from 4 pots of each cultivar to determine the distribution and type of calcuium oxalate crystals in each plant organ via polarized light microscopy. Two types of calcium oxlate crystals, raphides and druses, were found in the stem, leaves and roots. Druse density increased as leaves andd stems matured while the number of raphide idioblasts remained relatively constant. Crystal density was highest at lateral initation sites of buds and roots. Significant differences were found in crystal density among cultivars even though `Carina' and `Star Bright' are sports selected from `Camille'. This suggests that reduction of calcium oxalate density of Dieffenbachia cultivars is possible through breeding.

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Plant tissue culture can induce a variety of genetic and epigenetic changes in regenerated plantlets, a phenomenon known as somaclonal variation. Such variation has been widely used in the ornamental foliage plant industry as a source for selection of new cultivars. In ornamental aroids alone, at least 63 somaclonal-derived cultivars have been released. In addition to morphological differences, many somaclonal aroid cultivars can be distinguished by amplified fragment length polymorphism (AFLP) analysis. However, a few cultivars have no detectable polymorphisms with their parents or close relatives by AFLP fingerprints. It is postulated that DNA methylation may be involved in the morphological changes of these cultivars. In this study, methylation-sensitive amplification polymorphism (MSAP) technique was used to study DNA methylation in selected somaclonal cultivars of Alocasia, Aglaonema, Anthurium, Dieffenbachia, Philodendron, and Syngonium. Results showed that polymorphisms were detected in the somaclonal cultivars, suggesting that DNA methylation polymorphisms may associate with tissue culture-induced mutation in ornamental aroids. This is the first study of methylation variation in somaclonal variants of ornamental foliage plants. The results clearly demonstrate that the MSAP technique is highly efficient in detecting DNA methylation events in somaclonal-derived cultivars.

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Syngonium podophyllum ‘White Butterfly’, one of the most popular ornamental foliage plants, is propagated almost exclusively through in vitro shoot culture. Ex vitro rooting, however, has been associated with severe Myrothecium leaf spot (Myrothecium roridum Tode ex Fr.). The objective of this study was to establish a method for regenerating well-rooted plantlets before ex vitro transplanting. Leaf and petiole explants were cultured on a Murashige and Skoog (MS) basal medium supplemented with N-(2-chloro-4-pyridyl)-N′-phenylurea (CPPU), N-phenyl-N′-1,2,3-thiadiazol-5-ylurea (TDZ), 6-benzyladenine (BA), or N-isopentenylaminopurine (2iP) with α-naphthalene acetic acid (NAA) and 2,4-dichlorophenoxyacetic acid (2,4-D), respectively. Calli formed from leaf explants cultured on the basal medium supplemented with CPPU or TDZ with 2,4-D or with NAA as well as from petiole explants cultured on the medium supplemented with BA, CPPU, or TDZ with 2,4-D or NAA. The calli, however, failed to differentiate, and shoot organogenesis did not occur. Culture of nodal explants on the MS basal medium supplemented with 9.84 μm 2iP, 8.88 μm BA, 8.07 μm CPPU, or 9.08 μm TDZ with 2.26 μm 2,4-D resulted in the formation of protocorm-like bodies, adventitious shoots, and subsequently well-rooted plantlets. MS basal medium supplemented with 19.68 μm 2iP and 1.07 μm NAA resulted in the highest percentage (92.9%) of nodal explants producing protocorm-like bodies and an average of 16.9 well-rooted plantlets per nodal explant. Adventitious shoots were able to root in the initial induction medium, but better root development occurred after shoots with protocorm-like bodies were transferred onto MS basal medium supplemented with 9.84 μm 2iP and 2.69 μm NAA. Regenerated plantlets were stable and grew vigorously with 100% survival rates after ex vitro transplanting to a container substrate in a shaded greenhouse.

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Colchicine application successfully induced tetraploids from in vitro-cultured diploid Dieffenbachia × ‘Star Bright M-1’. Shoot clumps, each with six to eight small, undifferentiated shoot primordia, were cultured in liquid Murashige and Skoog (MS) medium and treated with colchicine at rates of 0, 250, 500, or 1000 mg·L−1 for 24 h. In vitro survival of shoot clumps significantly decreased as colchicine concentrations increased. Shoot clumps that survived were transferred to colchicine-free MS medium containing 2.0 mg·L−1 N6-isopentenyl) adenine and 0.10 mg·L−1 indole-3-acetic acid. Shoots were harvested during four subsequent subcultures and planted in a soilless substrate in a shaded greenhouse. The number of plants that survived 6 months after ex vitro planting was 690, 204, 59, and 69 for colchicine treatments at 0, 250, 500, and 1000 mg·L−1, respectively. The 332 plants from colchicine treatments along with 90 control plants (selected from 690 in the control treatment) were evaluated morphologically in a shaded greenhouse. Overall plant growth, including crown height, plant canopy, and leaf size, of colchicine-treated plants was significantly less than controls. Based on the growth data, 10, 32, 15, and 16 plants from the 0, 250, 500, and 1000 mg·L−1 colchicine rates, respectively, were selected and analyzed by flow cytometry. Flow cytometry confirmed the presence of 13 tetraploids and 29 mixoploids among the 63 colchicine-treated selections; all 10 plants from the control were diploid. A colchicine rate of 500 mg·L−1 produced a higher percentage of tetraploids (10.2%) than did the 250 (2.9%) or 1000 mg·L−1 (1.4%) rates. Subsequent comparisons showed tetraploids had significantly smaller and thicker leaves, greater specific leaf weights, and longer stomata than diploids. Tetraploids also showed increased net photosynthetic rate, decreased g S, decreased intercellular CO2 concentration, decreased transpiration rate, and increased water use efficiency. Tetraploids appeared robust and their smaller size could make them potentially more durable plants used as living specimens for interior decoration.

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‘Jincuilei’ is a mutant selected from Lonicera macranthoides Hand.-Mazz. It produces abundant flowers that never open with a chlorogenic acid (CGA) content up to 6.0%. Propagation through rooting or grafting has only a 30% survival rate. This study was undertaken to establish an efficient protocol for rapidly regenerating this mutant. Leaf explants were inoculated on Gamborg's B5 medium supplemented with different concentrations of 6-benzyladenine (BA) and 2,4-dichlorophenozyacetic acid (2,4-D). The optimal combination for callus induction was 4.4 μm BA with 2.26 μm 2,4-D, which resulted in 86.7% of leaf explants producing calluses in 4 weeks. Calluses produced from this optimal medium were cultured on B5 medium containing different concentrations of kinetin (KT) and α-naphthalene acetic acid (NAA). The best formulation for shoot induction was B5 medium containing 0.9 μm KT and 5.4 μm NAA in which 73.4% of cultured calluses produced shoots in 8 weeks, and shoot numbers ranged from three to six per callus piece (1 cm3). Adventitious shoots were cut and rooted in half-strength Murashige and Skoog medium supplemented with 14.8 μm 3-indolebutyric acid. Roots initiated 10 d after culture, and rooting percentages ranged from 98% to 100%. Plantlets grown in a container substrate in a shaded greenhouse had over a 95% survival rate. During the last 6 years, over four million plantlets were regenerated using this established procedure, and there was no somaclonal variation. Fresh and dry weights of 1000 flowers, CGA contents, and dry flower yields of the regenerated plants were not significantly different from those of the stock ‘Jincuilei’ propagated by cutting, indicating that plants regenerated from this established procedure were stable. This established in vitro culture method has led to rapid commercial production of this medicinal plant on more than 1500 ha of production field.

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