Ken W. Leonhardt
Erika Szendrák, Paul E. Read, Eszter R. Eszéki, Elizabeth Jámbor-Benczúi, and Aniko Csillag
Cultures of several orchid species [Barlia robertiana (Loisel.), Dactylorhiza fúchsii Soó, D. incarnata (L.) Soó, D. maculata (L.) Soó, D. majalis (Rchb.), D. saccifera (Brong) Soó, D. sambucina (L.) Soó, Gymnadenia conopsea (L.) R.Br., Himantoglossurn hircinum (L.) Spreng., Ophris sphegodes Mill., Orchis coriophora ssp. fragrans L., Orchis laxiflora ssp. palustris Lam., Orchis mascula L., Orchis morio L., Platanthera bifolia (L.) Rich., Spiranthes aestivalis (Poir.) Rich.] were initiated with fresh ripe seeds from desiccated fruit and 4-month-old in vitro seedlings. The medium used for both germination and seedling culture was a modified FAST medium. Samples for the scanning electron microscope (SEM) surveys were taken from the in vitro cultures and some plant materials were collected from their native habit. Samples were observed with a Tesla BS 300 SEM. Seeds ranged from 300 to 450 μm in length and were flask-shaped. The first germination step is opening of the seedcoat, when the first few white cells will be visible. After a few weeks, the apical meristem appears. The young protocorm is covered with numerous translucent rhizoids. In the last stage of germination, the first root and the first true leaf start to develop. After 2 years, they are suitable for transfer ex vitro. Structure of the mature organs and tissues can be examined at this stage.
Roberto G. Lopez and Erik S. Runkle
The vegetatively propagated `Fire Kiss' clone of the hybrid Zygopetalum Redvale orchid has appealing potted-plant characteristics, including fragrant flowers that are waxy lime-green and dark maroon with a broad, three-lobed, magenta and white labellum. We performed experiments to quantify how temperature influenced leaf unfolding and expansion, time from visible inflorescence to flower, and longevity of individual flowers and inflorescences. Plants were grown in controlled-environment chambers with constant temperature set points of 14, 17, 20, 23, 26, and 29 °C and an irradiance of 150 μmol·m-2·s-1 for 9 h·d-1. As actual temperature increased from 14 to 25 °C, the time to produce one leaf decreased from 46 to 19 days. Individual plants were also transferred from a greenhouse to the chambers on the date that an inflorescence was first visible or the first flower of an inflorescence opened. Time from visible inflorescence to open flower decreased from 73 days at 14 °C to 30 days at 26 °C. As temperature increased from 14 to 29 °C, flower and inflorescence longevity decreased from 37 and 38 days to 13 and 15 days, respectively. Data were converted to rates, and thermal time models were developed to predict time to flower and senescence at different temperatures. The base temperature was estimated at 6.2 °C for leaf unfolding, 3.5 °C for time to flower, and 3.7 °C for flower longevity. These models could be used by greenhouse growers to more accurately schedule Zygopetalum flowering crops for particular market dates.
Christine Yung-Ting Yen, Terri W. Starman, Yin-Tung Wang, Andreas Holzenburg, and Genhua Niu
Orchids have long been attractive plants to many people because of their wide variety of shapes and patterns, exotic colors, long-lasting flowers, and fragrance. The U.S. Department of Agriculture (USDA) reported that in the United States, the
Rebecca G. Bichsel, Terri W. Starman, and Yin-Tung Wang
The production of potted orchids has increased since the early 1990s because of advances in propagation and cultivation techniques and consumer demand. Orchids are recognized as a profitable crop by commercial growers ( Britt, 2000 ). In 2006, the
Elise A. Konow and Yin-Tung Wang
Presently, there are no standards for producing Phalaenopsis Blume (the moth orchids) as a flowering, potted crop. Determining optimal irradiance for in vitro and greenhouse production will help optimize growth and flowering. Four-month-old, aseptically propagated Phalaenopsis Atien Kaala seedlings with 1.0 cm leaf spread were transferred to a sterile agar medium in November 1995. They were placed under 10, 20, 40, or 80 μmol·m-2·s-1 photosynthetic photon flux (PPF) from cool-white fluorescent lamps. In June 1996, plants grown under 40 or 80 μmol·m-2·s-1 in vitro PPF had 38% greater fresh weight (FW), wider leaves, and more roots than those under the two lower PPF levels. Plants from each in vitro PPF were then transplanted and grown ex vitro in a greenhouse (GH) under high, medium, or low PPF, representing 12.0%, 5.4%, or 2.6% of full sunlight, respectively. Full sunlight at this location was 2300 and 1700 μmol·m-2·s-1 in August 1996 and January 1997, respectively. In November 1996 and June 1997, plants that had received 40 μmol·m-2·s-1 in vitro PPF and then grown under the high or medium GH PPF had the greatest FWs. Overall, plants under the high, medium, or low GH PPF had average FWs of 61, 36, or 17 g, respectively, in June 1997. By mid-September 1997, plants had increasingly larger leaves and higher concentrations of malic acid, sucrose, and starch as GH PPF increased. Leaf glucose and fructose concentrations remained constant as GH PPF increased; however, sucrose level doubled and malic acid concentration increased by nearly 50% from the low to high GH PPF. Each doubling in GH PPF more than doubled plant FW. Plants grown under the high, medium, or low GH PPF had 98%, 77%, or 2% flowering, respectively, in Spring 1998. Anthesis occurred 2 weeks earlier under the high GH PPF. Plants grown under the high GH PPF had twice as many flowers and larger flowers than those grown under the medium PPF.
V. P. E. Phang, U. Charanasri, and H. Kamemoto
The intersectional hybrids, Oncidium altissimum × O. sarcodes and O. floridanum × maculatum, and the intergeneric hybrid, Odontoglossum stenoglossum × O. macuiatum (all with 2n = 56), showed near normal meiosis with 27 or 28 bivalents per pollen mother cell indicating strong homology of parental genomes. Trichocentrum albopurpureum (2n = 24) × O. lanceanum (2n = 26) exhibited fair homology of parental genomes with the formation of 6 to 10 bivalents out of the possible 12. The other intersectional hybrids, O. pulvinatum (2n = 42) × O. floridanum (2n = 56), O. triquetrum (2n = 42) × O. floridanum (2n = 56), O. microchilum (2n = 36) × O. floridanum (2n = 56) and O. microchilum (2n = 36) × O. onustum (2n = 56) and the intergeneric hybrid, Comparettia falcata (2n = 42) × O. onustum (2n = 56) showed highly irregular meiotic behavior with poor chromosome pairing. The number of bivalents in these hybrids ranged from 1.4 to 9.5, indicating poor genome relationships of the parental species.
Ing-Jiun Tom Wu, G.L. Wheeler, and F.H. Huang
Scarification treatments (a control, a 10-minute vacuum, or a 1.5-minute ultrasound), different media (modified Norstog and Van Waes) and growth regulators [benzyladenine (BA) at 0, 1, 1.5, or 2 mg·L-1 and 6-(r,r-dimethylallylamino)-purine riboside (2iPR) at 0, 1, 1.5 or 2 mg·L-1] were used in combination to increase seed germination of Cypripedium calceolus var. parviflorum. Seeds treated with ultrasound had higher germination (58.0%) than those treated with vacuum (27.4%) or controls (19.2%). Germination rates increased with 2iPR level and reached a maximum between 1.5 and 2 mg·L-1. Seeds on Van Waes medium, which were not transferred to fresh medium after germination, had a severe browning problem causing many protocorms to die. Those on Norstog medium continued to grow into seedlings with less browning. Germination rates of Calopogon tuberosus × Calopogon `Adventure' and Liparis liliifolia were determined on the different media and growth regulator treatments. Multiple shoots of Calopogon developed from single seeds on media containing growth regulators. Flower buds formed in vitro on Calopogon in media containing 1 mg·L-1 or higher BA 5 months after germination. L. Iiliifolia seeds in Norstog medium had a higher proportion of germination than those in Van Waes medium.