Cultural Studies in Ornamental Ginger

Similar documents
Response Of Blueberry To Day Length During Propagation

Evaluation of Chlormequat and Daminozide Products on Greenhouse Crops

Cytokinin treatment and flower quality in Phalaenopsis orchids: Comparing N-6-benzyladenine, kinetin and 2- isopentenyl adenine

Propagation and Production of Zamioculcas zamiifolia

Alert. Flowering of Begonias Sponsors

prgperly cooled lily bulbs from potting to flowering was a 70 F. day temp (DT)/

Effect of Temperature and Pseudobulb Maturity on Flowering of the Orchid Miltoniopsis Augres Trinity

Garden Mum Crop Scheduling October 3, 2018 Mark Smith

Tuberous root development and flower induction of. Manipulating DAHLIAS. By Garry Legnani and William B. Miller. crop cultivation

The Problem ADVANCED TECHNIQUES IN CUT FLOWER PRODUCTION: INCREASING STEM LENGTH AND STRENGTH. Where Are You Growing It? What Can I Do About It?

INFLUENCE OF PHOTOPERIOD ON IMPROVED 'WHITE SIM' CARNATION (DIANTHUS C A R Y O P H Y L L U S L.) BRANCHING AND FLOWERING

Let light motivate your flowers

Shock Wave Petunia. P. x hybrida Seed Count (Pelleted): 33,000 S./oz. (1,200 S./g)

DIFFERENTIATION OF AVOCADO BLOSSOM BUDS IN FLORIDA

CONTROLLING CHRYSANTHEMUM FLOWERING BY ALTERING DAYLENGTH

Using Gibberellic Acid and Ethephon to Induce Flowers on Tropical Foliage Plants1

Reprinted from Vol. 107(2), March 1982 Journal of the American Society for Horticultural Science Alexandria, Virginia 22314, USA

Effects of Fertilizer Formulations on Flowering of Doritaenopsis I-Hsin Madame in Gradational Nutrition Management

Effect of Ethephon on Easy Pot Freesia

Growth and development of plants influenced by: Genetic factors External environmental factors Chemicals Plants respond to chemicals that are

FIGURE 15 1 The structure of a tulip bulb an example of a tunicate laminate bulb. Longitudinal section representing stage of development shortly

232 J. Amer. Soc. Hort. Sci. 116(2):

MY BACKGROUND. Saeid since 1998

Photoperiodic Control of Growth and Development in Nonstop Cultivar Series of Begonia x Tuberhybrida

This article is the third

EVALUATION OF AVOCADO COLD HARDINESS

By the time you read this article, Easter lilies will have been planted, Easter Lilies: Easter Lilies: A Challenge You Can Master

Papaver Alboroseum Portage Poppy. Katie Shields Hort 5051 May 4, 2005

Effect of gibberellic acid treatments on flowering of avocado

Kabloom and Crave Calibrachoa. Plug and Finish Culture

in Ginger (Zingiber officinale

IPC 24th Session, Dehradun Nov 2012

MNLA Certification Manual Learning Objectives

PRACTICE EXAM HORT 201 2nd EXAM from Fall 1999

UNIVERSITY OF CALIFORNIA, RIVERSIDE. Botany. Department of. and. Plant Sciences.

Structures and Functions of Living Organisms

3 Plant Development and Responses

Lanthanum Effects on Gravitropic Response of Cut Tulip Flowers

HORTSCIENCE 39(1):

Center for Applied Horticultural Research (CfAHR) Research Report. Lucia Villavicencio 1. Prepared for: Fine Americas, Inc.

HORTSCIENCE 43(2):

THE STEMS. Botany nomenclature cards #24 - #34. 3 x 5 cards, blank labels, black pen. 2. Refer to 'The Plant' wall chart and point out the stem.

PP71DR EXPERIMENTAL SUMMARY Spring Comparison of PGRs for Drench Applications on Sensitive Perennials

Research Newsletter no. 31. by Bill Miller Cornell University, Ithaca NY

The first calibrachoas

Controlling Sedges in Landscape Plantings. Joseph C. Neal, Extension Specialist, Weed Management Department of Horticultural Science

Unit C: Plant Physiology. Lesson 2: Understanding Light, Temperature, Air, and Water Effects on Plant Growth

ORNAMENTALS NORTHWEST ARCHIVES

CAMBIUM, meristem, heartwood, and lenticel are

Commercial Greenhouse and Nursery Production

Plant Profiles: HORT 2242 Landscape Plants II

Plant Growth and Development Part I. Levels of Organization

APPLICABILITY OF THE USE OF AEROPONIC SYSTEM AND SILICON SUPPLEMENTATION ON GROWTH AND THE FLORICULTURAL QUALITY TRAITS OF Dendrobium sp.

Learning objectives: Gross morphology - terms you will be required to know and be able to use. shoot petiole compound leaf.

Light. Bedding Plants

Horticulture 201H Spring, 2002 Exam 2 Name:

FINAL REPORT TO MICHIGAN DEPARTMENT OF AGRICULTURE AND RURAL DEVELOPMENT HORT FUND PROJECT FY 2015

Botany Physiology. Due Date Code Period Earned Points

PLSC 210-Horticulture Science Examination II October 23, is a plant hormone responsible for apical dominance.

Snapdragon Lighting. Harrison Flint. Cornell University. ing mid-winter. Several good approaches to this problem

Flowering of the Orchid Miltoniopsis Augres Trinity is Influenced by Photoperiod and Temperature

Breeding and Genetics

Propagation by Specialized Stems and Roots

Levels of Organization

EFFECTS OF CROP LOAD ON VEGETATIVE GROWTH OF CITRUS

Ch 25 - Plant Hormones and Plant Growth

INFLUENCE OF TEMPERATURE, RADIATION AND PHOTOPERIOD ON DEVELOPMENT AND YIELD

Improving Product Quality and Timing of Kalanchoe: Model Development and Validation

Objectives of presentation Advanced PGR Use Annuals Dr. Royal D. Heins Poor rooting check the following

Trees are: woody complex, large, long-lived self-feeding shedding generating systems compartmented, self optimizing

Chapter 15 PLANT STRUCTURES AND TAXONOMY

How Plants Grow HOME GARDENING OSHER LIFELONG LEARNING SPRING 2015

Chemical Approach to Branching. Branching Agents on Herbaceous Perennial Plugs. Echinacea Doubledecker. Application Timing (Margaret Tackett)

Studies on the Light Controlling Flower Initiation of Pharbitis Nil. VI. Effect of Natural Twilight. by Atsushi TAKIMOTO* and Katsuhiko IKEVA*

Developing Off-season Production Technique for Rambutan

Identifying Wheat Growth Stages

Catasetum and Cycnoches Part 5 Growth Cycle

Structures and Functions of Living Organisms

Invasive Species Management Plans for Florida

IR-4 Ornamental Horticulture Program Trial Report

Effects of photoperiod and temperature on growth and flowering in the annual (primocane) fruiting raspberry (Rubus idaeus L.

Study on Purple Nutsedge (Cyperus rotundus) Tuber Dormancy and its Control Through Combined Application of Growth Regulator and Herbicides

Plant Juvenility Text Pages: 15 18,

E#ect of Daylength on the Flower Bud Di#erentiation and Development in Coriander (Coriandrum sativum L.)

ACCURACY OF MODELS FOR PREDICTING PHENOLOGY OF BLACKHEADED FIREWORM AND IMPLICATIONS FOR IMPROVED PEST MANAGEMENT

THE ECOLOGY AND CULTIVATION OF TERRESTRIAL ORCHIDS OF ARGENTINA

PHOTOPERIOD CONTROL OF CONTAINER SEEDLINGS. James T. Arnott

A Review of Winter Chilling Requirements in Pecan. Eric T. Stafne Associate Extension and Research Professor Mississippi State University

Understanding Light, Temperature, Air, and Water Effects on Plant Growth

CONTROL SYSTEMS IN PLANTS

HRI s Mission: Copyright, All Rights Reserved

of days to flower becomes the rate of progress toward flowering. Developmental rate is zero at or below a species-specific base temperature (T b

Basic Principles of Plant Science EXAMINING PLANT STRUCTURES AND FUNCTIONS

Plant Organization. Learning Objectives. Angiosperm Tissues. Angiosperm Body Plan

Parasitic Diseases. Plants killing plants

Critical photoperiod for short-day induction of flowering in black currant (Ribes nigrum L.)

Effects of bulb temperature on development of Hippeastrum

Reproduction, Seeds and Propagation

Cryotherapy: A New Method to Eliminate Pathogens from Sweetpotato Propagation Materials

Desert Plant Adaptations

Transcription:

Reprinted from: Trends in new crops and new uses. 2002. J. Janick and A. Whipkey (eds.). ASHS Press, Alexandria, VA. Cultural Studies in Ornamental Ginger Jeff S. Kuehny, Mauricio J. Sarmiento, and Patricia C. Branch INTRODUCTION Hedychium species (butterfly ginger) and Alpinia erumbet (shell ginger) have been grown in the Southern United States since at least the turn of the century (Burch 1998). Curcuma and Kaempferia are two other genera in the Zingiberaceae family that have recently gained much notoriety. Kaempferia species have unique foliage and Curcuma species colorful, long-lasting inflorescences, both with a 90- to 100-day production cycle and few pest problems. These gingers have great potential for use as flowering pot plants, both indoors and as patio and landscape plants. They are herbaceous perennials with short fleshy rhiomes and tuberous roots, often with a dormancy period (Burch et al. 1987). Inflorescence stalks arise either from a short pseudostem or independently from buds on the rhiome. The inflorescence of Curcuma species are a compressed spike of colorful long lasting bracts subtending 2 to 7 true flowers (Luc-Cayo and Fereol 1997). Kaempferia species, however, have short lived flowers with attractive, colored/patterned leaves that vary in sie and shape. Burch (1998) reported that between 150,000 to 250,000 rhiomes of ginger would be sold in 1998. Because of the new genera of ginger continuing to enter the market, the value of ornamental ginger has not been well documented. The number of rhiomes sold has probably doubled (E. Welch, pers. commun.) since 1998 and this does not account for number of plants sold from tissue culture. There is little information on the optimum production environment, postproduction longevity, and landscape survivability of commercially available gingers. The objectives of this research were to determine the effects of light intensity, photoperiod, and plant growth regulator application on various cultures of Curcuma and Kaempferia species (Fig. 1 5). METHODOLOGY All plants were grown in the greenhouse using a medium consisting of 1/2 peat moss, 1/3 pine bark, and 1/6 perlite, amended with dolomite limestone (5.1 kg/m 3 ) and superphosphate 0 18 0 (2.7 kg/m 3 ). Immediately after planting containers were drenched with a tank mix of metalaxyl (Subdue 2E, Novartis, Greensboro, North Carolina) at 15.6 ml/ 100 L and PCNB quintoene (Terraclor 75% WP, Uniroyal Chemical, Middlebury, Connecticut). Plants were spaced on 21 21 cm centers and fertigated with 24N 3.5P 13.3K (Peters 24 8 16 Tropical Foliage, Scotts-Sierra, Marysville, Ohio) at Fig. 4. petiolata. Curcuma Fig. 1. Curcuma alismatifolia Chiang Mai Pink Fig. 2. Curcuma spp. Precious Petuma Fig. 3. Curcuma cordata. Fig. 5. Kaempferia spp. Grande. 477

Trends in New Crops and New Uses 150 ppm N as needed. Data was analyed using PROC GLM. Comparisons between means was conducted by Tukey s studentied range test. Light Levels and Plant Growth Retardants Curcuma spp. Precious Petuma, C. parviflora White Angel, and C. alismatifolia Chiang Mai Pink rhiomes were planted one per 14 cm container on 4 April 2000. Plants were grown in a greenhouse at temperature setpoints of 27 /21 C day/night. When shoot height was 10 cm, the plants were drenched with 118 ml of paclobutraol or uniconaole at 0, 10 or 20 mg a.i. per container and grown under a 0% (1,860 µmol/s/ m 2 ), 30% (922 µmol/s/m 2 ) or 60% (352 µmol/s/m 2 ) shade. Average daily temperatures for the three light levels were 30 C. Days to emergence, days to bloom, number of flowers, height of the flowering stalk, and days to anthesis (postproduction longevity) were determined for all plants. There was no significant effect of shade level on days to emergence or days from emergence to first flower for Curcuma spp. Precious Petuma. Flower height was 22% taller for those plants grown under both shade levels. Application of paclobutraol and uniconaole at 20 mg a.i./pot reduced the flower height of Precious Petuma by 27% and 54% respectively. Because flower height was acceptable (approximately 25 cm) at all shade levels, the use of a growth retardant is not recommended. Shade level had no affect on flower longevity, with an average 29 day postproduction longevity. The number of days from first flower to second flower were extended by approximately 12 days when plants were grown under 60% shade. Days from emergence to first flower of C. parviflora White Angel was significantly extended by approximately 13 days when grown under 60% shade. Flower height was 23% taller at 30% shade; however, due to the short stem of this flower, this height was still acceptable (less than 25 cm). Thus, the use of a growth retardant is unnecessary. Shade level did not affect flower longevity or days to second flower. Flower longevity was favorable at approximately 30 days and days to second flower was approximately 40 days for all treatments. Days from planting to emergence and emergence to first flower of C. alismatifolia Chiang Mai Pink were unaffected by shade level or rate of growth retardant. Days from first flower to second flower was significantly extended by both shade levels with no second flower produced at 60% shade. Thus, these plants must be grown under full sun for best quality. When grown at 30% or 60% shade, flower height was significantly taller by 9 and 13 cm respectively. The flower height of these plants, regardless of shade treatment, was not of marketable quality. The results from this study indicate that for production of a marketable flowering Chiang Mai Pink ginger, application of uniconaole at 10 mg a.i./pot and a rate greater than 20 mg a.i./ pot of paclobutraol is recommended. Postproduction longevity of this ginger is approximately 40 days. Gibberellic Acid Curcuma alismatifolia Chiang Mai Pink, C. gracillima Violet, and C. thorelii one cm rhiomes were planted one per 14 cm container on 17 April 1999. Prior to planting, rhiomes were soaked for 10 min in a solution containing 2% GA 4+7 (Provide, Abbot Labs, North Chicago, Illinois) at 0, 200, 400, or 600 mg/l, 10% Physan 20 (10% dimethyl benyl ammonium chloride, 10% dimethyl ethyl ammonium chloride, 80% inert, Maril Products, Tustin, California) and distilled water. Rhiomes were dried and planted in a greenhouse with average minimum and maximum temperatures of 23 and 30 C night/day. Treatments were arranged in a complete randomied design. Plants were harvested once a week when they reached a stage characteried by the opening of the last bract and one flower (marketable stage). Days to bloom, number of flowers, and height of the flowering stalk were recorded for all plants. GA at 200, 400, and 600 ppm delayed shoot emergence of C. alismatifolia Chiang Mai Pink (Table 1). GA at 400 ppm delayed flowering but did not increase the number of inflorescences. All plants had one inflorescence per container. Application of GA at 600 ppm reduced flower height (data not shown). GA concentrations of 600 ppm delayed shoot emergence of C. gracillima Violet and C. thorelii (Table 1). Days to bloom and flower height was unaffected for either Curcuma, and plants developed no more than one flowering stem. 478

Ornamentals Table 1. Effect of gibberellic acid (GA) on days to emergence and days to bloom of Curcuma alismatifolia Chiang Mai Pink, C. gracillima Violet, and C. thorelii. Days to emergence Days to bloom Curcuma Curcuma Curcuma Curcuma Curcuma Curcuma GA (ppm) alismatifolia gracillima thorelii alismatifolia gracillima thorelii 0 43.5 a 40.5 a 40.2 a 113 a 108 a 113 a 200 53.1 b 44.6 ab 43.7 ab 115 ab 114 a 115 a 400 57.1 b 44.6 ab 45.0 ab 128 b 109 a 113 a 600 55.4 b 47.9 b 51.2 b 126 ab 121 a 131 a Mean separation of GA rates by HSD test, P=0.05. Means within columns with different letters are significantly different. Photoperiod Tissue culture plants of Curcuma petiolata Emperor, C. thorelii, and Kaempferia sp. Grande were planted one per 15 cm container in the greenhouse on 16 Aug. 1999. Tissue culture plants of C. cordata were planted two per 15 cm container on 9 Sept. 1999. Rhiomes of C. alismatifolia Siam Tulip White were planted one per 12.5 cm container on 27 Aug. 1999. All ginger species were arranged in a complete randomied design under each photoperiod treatment. Photoperiod treatments were initiated 17 d after transplanting for C. alismatifolia C. petiolata, C. thorelii, and Kaempferia sp. Grande and 18 d after transplanting for C. cordata. On 2 Sept. 1999 photoperiod treatments of 8, 12, 16, and 20 hr were initiated. Plants received 8 hr of natural light from 0900 to 1700 hr. Zero, four, eight, and twelve hours of supplemental light were provided for the 8, 12, 16, and 20 hr photoperiod, respectively. Light source was 100 watt incandescent light bulbs at an irradiance of 11 µmol/s/m 2 (14 to 50 foot candles). Average minimum and maximum temperatures were 18 and 26.5 C. Curcuma petiolata, C. thorelii, Emperor, and Kaempferia sp. Grande completed 21 weeks in the photoperiod treatment, C. cordata was 19 weeks and C. alismatifolia 18 weeks. Each week, the number of newly unfolded leaves was counted as a measurement of plant growth. On 1 Dec. 1999, the height of the plants was measured from the medium surface to the tip of the longest leaf. On 1 Feb. 2000, the photoperiod treatment ended. Plants which did not go dormant during the course of the experiment were forced to dormancy by terminating irrigation. After all plants were dormant, the number of rhiomes and t-roots was counted for each treatment. Dormancy was induced on all ginger grown under an 8 hr photoperiod. The number of weeks required for plants to go dormant under an 8 hr photoperiod was 9.0±0.17 weeks for C. cordata, 15±0 weeks for C. petiolata, 11.6±1.2 weeks for C. thorelii, and 12±0 weeks for Kaempferia. Plant height of C. alismatifolia increased as length of photoperiod increased to 20 h (Table 2). Curcuma cordata plants grown at 20 and 16 hr were significantly taller than plants grown at 12 hr. Plants grown at 8 hr became dormant. Curcuma petiolata plants grown under 8 and 12 hr were significantly shorter than plants under 20 and 16 hr. Curcuma thorelii plants grown under 16 and 20 hr were significantly taller than plants at 12 hr. There were no significant differences in height between 12, 16, and 20 hr treatments for Kaempferia. The number of leaves unfolded increased during the 16 and 20 hr photoperiod for C. alismatifolia (Table 3). Curcuma cordata plants under 16 and 20 hr photoperiods produced more new leaves than 8 and 12 hr photoperiods. Curcuma petiolata Emperor plants grown at 16 and 20 hr produced more new leaves than plants grown at 8 and 12 hr (Table 3). Photoperiod did not significantly affect the number of new leaves C. thorelii produced. Kaempferia sp. Grande plants in the 16 and 20 hr photoperiod produced more new leaves than those in 8 hr. Curcuma alismatifolia, C. cordata, and C. petiolata plants grown under 16 and 20 hr produced a greater number of rhiomes than those plants grown under 8 and 12 hr (Table 4). Photoperiod did not affect the number of rhiomes produced by C. thorelii or Kaempferia. Curcuma alismatifolia grown under a photoperiod of 16 hr or less produced approximately two t-roots per plant and approximately one t-root at 20 hr (Table 5). 479

Trends in New Crops and New Uses Table 2. Effect of photoperiod on plant height for Curcuma alismatifolia Chiang Mai White, C. cordata, C. petiolata Emperor, C. thorelii, and Kaempferia sp. Grande. Plant height (cm) 8 20.7 a dormant y 35.6 a dormant dormant 12 30.0 b 42.7 a 41.6 a 32.0 a 31.6 a 16 38.8 c 50.2 b 65.3 b 37.3 b 46.6 a 20 35.6 bc 49.0 b 70.3 b 38.0 b 46.6 a y Plants were dormant prior to measurement. Table 3. Effect of photoperiod on total number of new leaves unfolded Curcuma alismatifolia Chiang Mai White, C. cordata, C. petiolata Emperor, C. thorelii, and Kaempferia sp. Grande. Number of leaves unfolded 8 1.6 a 0.5 a 2.6 a 2.0 a 2.0 a 12 2.1 a 2.8 a 3.3 a 4.6 a 3.3 ab 16 6.8 b 10.0 b 17.3 b 4.3 a 10.0 c 20 8.6 c 9.1 b 21.0 b 5.3 a 8.6 bc Table 4. Effect of photoperiod on number of rhiomes of underground organs for Curcuma alismatifolia Chaing Mia White, C. cordata, C. petiolata Emperor, C. thorelii, and Kaempferia sp. Grande. Number of rhiomes 8 1.0 a 1.0 a 1.0 a 1.0 a 1.0 a 12 1.0 a 1.0 a 1.0 a 1.0 a 1.0 a 16 1.9 b 1.9 b 1.6 ab 1.0 a 1.0 a 20 2.3 c 2.1 b 3.0 b 1.0 a 1.3 a Curcuma cordata, C. petiolata, and Kaempferia produced approximately 5 t-roots or more when grown at a photoperiod of 12 and 8 hr, and almost no t-roots at 16 and 20 hr. Curcuma thorelii responded to changes in photoperiod by producing a large number of t-roots for all treatments, producing the greatest number of t- roots at 16 hr. 480

Ornamentals Table 5. Effect of photoperiod on number of t-roots of underground organs for Curcuma alismatifolia Chaing Mia White, C. cordata, C. petiolata Emperor, C. thorelii, and Kaempferia sp. Grande. Number of t-roots 8 2.1 b 5.9 a 6.3 b 6.0 a 8.3 b 12 2.1 b 5.3 a 6.3 b 8.3 ab 4.6 b 16 1.9 b 0.0 b 0.3 a 11.6 b 0.0 a 20 0.6 a 0.0 b 0.6 a 10.6 ab 0.0 a CONCLUSIONS Curcuma spp. Precious Petuma, C. parviflora White Angel, and C. alismatifolia Chiang Mai Pink produce marketable flowering pot plants requiring no application of shade. Precious Petuma and White Angel can be grown under shade levels of up to 60% without use of growth retardant and no deleterious affect on plant quality. Chiang Mai Pink should be grown in full sun and an application of either 10 mg a.i./ pot of uniconaole or over 20 mg a.i./pot of paclobutraol for production of a quality flowering pot plant. These ornamental gingers have an excellent postproduction longevity of up to 40 days. GA did not increase the number of inflorescences of Curcuma alismatifolia but did delay shoot emergence and flowering. GA applied (as a spray) at concentrations of 1.44 and 2.88 mm suppressed shoot emergence of field grown edible ginger (Zingiber officinale Roscoe) (Furutani and Nagao 1986). GA usually stimulates stem lengthening however, GA at 600 ppm significantly reduced flower height of C. alismatifolia. Soaking rhiomes in GA at 200, 300, 400, and 600 ppm did not inhibit shoot sprouting but delayed it. GA has been recommended for extending dormancy, thereby inhibiting sprouting in storage of yams (Dioscorea cayenensis rotundata Lam. and D. alata L.), an edible tuber (Girardin et al. 1998). Thus, GA could be used to prolong storage of ornamental ginger rhiomes prior to planting. It should not be used to promote or increase flowering. Photoperiod affected height of all species of ginger evaluated. The plants grown under 20 or 16 hr photoperiods were taller than those grown under 12 or 8 hr photoperiods. Photoperiod affected the number of unfolded leaves of all plants except for C. thorelii. The 16 and 20 hr photoperiods increased number of leaves unfolded compared to 12 and 8 hr. Effect of photoperiod on number of rhiomes and number of t-roots was dependent upon the species of ginger. Kaempferia sp. Grande, C. petiolata, C. cordata, and C. alismatifolia Siam Tulip White produced more t-roots when grown under 8 or 12 hr than 20 or 16 hr photoperiods. The exception was C. thorelii, where more t-roots where produced on the plants growing at 20 or 16 hr photoperiod than in 12 or 8 hr. Siphonichilus decora did not produce t-roots under any of the 4 photoperiods. Curcuma petiolata, C. cordata, and C. alismatifolia Siam Tulip White produced more rhiomes under the long day photoperiods (20 and 16 hr) than under 12 or 8 hr. Ginger shoot and rhiome growth were optimied when plants were grown under 16 or 20 hr photoperiods, whereas an 8 hr photoperiod promoted dormancy. The best production strategy for growers of gingers as flowering potted plants is to plant in the spring (April) and grow the plants throughout the summer, finishing production in the fall. If production in the winter is desired, 16 hr photoperiod must be used. REFERENCES Burch, D. 1998. The commercial market for gingers in the U.S. Heliconia Soc. Int. Bul. 9(3):1 4. Burch, D., E.W. Demmy, and H. Donselman. 1987. Gingers for Florida gardens. Proc. Fla. State Hort. Soc. 100:153 155. 481

Trends in New Crops and New Uses Fereol, L., S. Louis, and L. Luce. 1996. Effects of gamma radiation on in vitro plantlets of Alpinia purpurata. J. Hort. Sci. 71:243 247. Furutani, S.C. and M.A. Nagao. 1986. Influence of daminoide, gibberellic acid and ethephon on flowering, shoot growth and yield of ginger. HortScience 21:428 429. Girardin, O., C. Nindjin, Z. Farah, F. Escher, P Stamp, and D. Otokore. 1998. Use of gibberellic acid to prolong dormancy and reduce losses during traditional storage of yams. J. Sci. Food Agr. 77:172 178. Luc-Cayo F. and L. Fereol. 1997. Alpingera martinica (Zingiberaceae): An intergeneric hybrid between Alpinia purpurata and Etlingera elatior. HortScience. 32(5):914 915. 482