cold temperatures as necessary for vernalization in biennial vegetables like cabbage or kale; however, few realize that many cultivars of broccoli have a quantitative cold requirement needed to induce flowering ( Fontes et al., 1967 ). Whereas cabbage
Mark W. Farnham and Thomas Bjorkman
J. Ryan Stewart, William R. Graves and Reid D. Landes
Carolina buckthorn [Rhamnus caroliniana Walt. or Frangula caroliniana (Walt.) Gray] is an attractive and water-stress-resistant shrub or small tree distributed extensively in the southeastern United States that merits use in managed landscapes. Due to substantial climatic differences within its distribution (30-year normal midwinter minima range from 13 to -8 °C), selection among provenances based on differences in cold hardiness is warranted. Before selections are marketed, the potential of carolina buckthorn to be invasive also merits investigation. Ecological problems resulting from the introduction of Rhamnus L. species in the United States, most notably the dominance of R. cathartica L. (common buckthorn) over neighboring taxa, are due in part to early budbreak. Consequently, we investigated depth of cold hardiness and vernal budbreak of carolina buckthorn and common buckthorn. Stem samples of carolina buckthorn and common buckthorn collected in midwinter survived temperatures as low as -21 and -24 °C, respectively. Although the cold hardiness of carolina buckthorns from Missouri was greater than that of carolina buckthorns from Ohio and Texas on 2 Apr. 2003, there were no differences in cold hardiness of stems from Missouri and Texas on all three assessment dates in the second experiment. All plants survived at both field locations except for the carolina buckthorns from southern Texas planted in Iowa, which showed 0% and 17% survival in 2003 and 2004, respectively. Budbreak of both species with and without mulch in Ames, Iowa, was recorded from 9 Apr. to 10 May 2002. Mean budbreak of common buckthorn was 5.7 days earlier than budbreak of carolina buckthorn, and buds of mulched carolina buckthorns broke 4.2 days earlier than did buds of unmulched carolina buckthorns. We conclude that the cold hardiness of carolina buckthorn is sufficient to permit the species to be planted outside of its natural distribution. Populations of carolina buckthorn in Ohio and Missouri should be the focus of efforts to select genotypes for use in regions with harsh winters. Phenology of its budbreak suggests carolina buckthorn will not be as invasive as common buckthorn, but evaluation of additional determinants of invasiveness is warranted.
Yuan-Tsung Chang, Der-Ming Yeh and Wen-Ju Yang
Statice [ Limonium sinuatum (L.) Mill.] is commercially grown as a cut-flower crop and used for both fresh and dry flower arrangements. Exposure to low temperatures at 11 ± 2 °C at the seedling stage promotes flowering. Vernalization requirements
John Erwin, Rene O’Connell and Ken Altman
were moved to a lighting treatment greenhouse (22/18 °C day/night temperature) for 6 weeks. A 5 °C cooling treatment temperature is in the optimal range (4–6 °C) for vernalization and overcoming dormancy, and 12 weeks is the maximum time many species
Grete Waaseth, Roar Moe, Royal D. Heins and Svein O. Grimstad
Varying photothermal ratios (PTR) were supplied to Salvia ×superba Stapf `Blaukönigin' during pre-inductive vegetative development with the exception of a short germination period under uniform conditions. In addition, both unvernalized plants and plants receiving a saturating vernalization treatment of 6 weeks at 5 °C were given two photosynthetic photon flux (PPF) levels (50 or 200 μmol·m-2·s-1) during subsequent inductive 16-hour long days. There were no effects of PTR treatments during vegetative development on subsequent flowering. However, the higher PPF level during inductive long days significantly accelerated floral evocation in unvernalized plants, lowering the leaf number at flowering. The effect was practically negligent after the vernalization requirement was saturated. In a second experiment, varying periods (4, 7, 10, and 14 days or until anthesis) at a PPF of 200 μmol·m-2·s-1 during 20-hour days were given at the beginning of a long-day treatment, either with or without preceding vernalization treatment. Flowering percentage increased considerably as the period at 200 μmol·m-2·s-1 was extended compared with plants grown at a lower PPF of 50 μmol·m-2·s-1. However, the leaf number on flowering plants was not affected, except in unvernalized plants receiving the highest PPF continuously until anthesis, where leaf number was reduced by almost 50%. We propose that the PPF-dependent flowering is facilitated either by the rate of ongoing assimilation or rapid mobilization of stored carbohydrates at the time of evocation. Abortion of floral primordia under the lower PPF (50 μmol·m-2·s-1) irrespective of vernalization treatment indicates that the assimilate requirement for flower bud development is independent of the mechanism for floral evocation.
Timothy A. Prince and Maria S. Cunningham
Lining of shipping cases with low-density polyethylene (PE) greatly reduced moisture loss from packing media and bulbs of Lilium longjlorum Thunb. `Nellie White' during shipping, handling, and case vernalization (CV). Three years of studies showed that use of PE liners accelerated floral sprout emergence above the growing medium, floral bud initiation, and flowering date. Effects of case lining became more pronounced as the initial water content of the spagnum peat packing was lowered. Case lining sometimes increased apical meristem diameters measured immediately after vernalization, or 2 or 4 weeks after bulb planting, but flower bud number was never significantly increased. Root growth during the first 4 weeks after planting was not affected by case lining. Bulb scale and basal plate water contents at planting were greater in lined than nonlined cases and when packed in peat of relatively high moisture content. Handling and vernalization of bulbs in PE-lined cases without a packing medium resulted in similar bulb forcing characteristics as in bulbs held in PE-lined cases packed with sphagnum peat.
M.W. Farnham and J.T. Garrett
Winter production of collard and kale (Brassica oleracea L. Acephala Group) in the southeastern United States is limited by the tendency of these leafy green vegetables to bolt following vernalization. Collard and kale cultivars, landraces, and breeding lines were tested in four winter environments from 1992 to 1995 to determine differences among all included entries for winter production and tendency to bolt in a cold season environment. Essentially all entries survived the conditions of four winter environments. However, whether an entry reached harvest size depended on its date of 50% bolting. Collard typically bolted earlier than kale. Most kale entries reached a marketable size before bolting, while only the collard cultivars `Blue Max' and `Champion' and landraces G. Summersett and Mesic Zero consistently did the same. Several entries, for example, `Squire' kale and G. Summersett collard, usually did not bolt. Results of this research indicate that significant genetic control of the long-standing (delayed bolting) phenotype is present in collard and kale. Successful winter production of these cole crops can be better ensured by using a long-standing genotype.
John E. Erwin and Gerard Engelen-Eigles
Interaction between simulated shipping and rooting temperature and harvest year was studied on Lilium longiflorum. Bulb dormancy and maturity appear to be separate phenomenon and are affected by temperature differently. Shoot emergence (an indicator of release from dormancy) was hastened by 10 °C shipping and 10 to 20 °C rooting temperatures in both years. Flower induction was affected differently by simulated shipping and rooting temperatures during 1992 and 1993, indicating that bulb maturity differed between the 2 years. Final leaf and flower number decreased because of shipping or rooting temperature, but only when bulbs were mature and received cool temperatures (<16 °C) before a 6-week vernalization treatment. Immature bulbs (at harvest) are unresponsive to vernalizing shipping and rooting temperatures. Prevernalization handling temperature and vernalization treatment length should vary with year based on degree of bulb maturity to achieve consistency in final morphology. Internode length is associated more with the time elongation is suppressed after dormancy is broken than with flower induction (where internode length increases as the length of time elongation is suppressed after breaking of dormancy increases).
Kil Sun Yoo and Leonard M. Pike
Catherine M. Whitman, Royal D. Heins, Arthur C. Cameron and William H. Carlson
The influence of cold treatments and photoperiod on flowering of 8- to 11-node and 18- to 23-node Lavandula angustifolia Mill. `Munstead' plants from 128-cell (10-mL cell volume; P1) and 50-cell (85-mL cell volume; P2) trays, respectively, was determined. Plants were stored at 5 °C for 0, 5, 10, or 15 weeks, then forced under a 9-h photoperiod (SD), or under a 4-h night-interruption (NI) (2200 to 0200 hr) photoperiod at 20 °C. Percentage of plants flowering, time to flower, and plant appearance were evaluated. Increasing duration of cold treatment was associated with an increase in flowering percentage in plants from both cell sizes. More plants flowered under NI than SD except in P2 cooled for 15 weeks, where all plants flowered. Average time to visible bud (VB) and to opening of the first flower (FLW) generally decreased with increasing duration of cold treatment. Inflorescence count in P2 plants increased with increasing duration of cold treatment. To determine the relationship between forcing temperature and time to flower in L. angustifolia `Munstead', three sizes of plants were exposed to 5 °C for 13 weeks and then forced under a 4-h NI (2200 to 0200 hr) at 15, 18, 21, 24, or 27 °C. Plants generally flowered more quickly at higher temperatures, time to FLW decreasing from 77, 71, and 60 days at ≈15.6 °C to 46, 40, and 36 days at ≈26 °C for P1, P2, and 5.5-cm (190-mL pot volume) (P3) plants, respectively. Generally, P1 plants flowered 5 to 10 days later than P2, and P2 flowered 5 to 10 days later than P3.