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For many long-day plants (LDP), adding far red light (FR, 700 to 800 nm) to red light (R, 600 to 700 nm) to extend the day or interrupt the night promotes extension growth and flowering. Blue light (B, 400 to 500 nm) independently inhibits extension growth, but its effect on flowering is not well described. Here, we determined how R-, FR-, or B-deficient (Rd, FRd, or Bd, respectively) photoperiods influenced stem extension and flowering in five LDP species: Campanula carpatica Jacq., Coreopsi ×grandiflora Hogg ex Sweet, Lobelia ×speciosa Sweet, Pisum sativum L., and Viola ×wittrockiana Gams. Plants were exposed to Rd, FRd, Bd, or normal (control) 16-hour photoperiods, each of which had a similar photosynthetic (400 to 700 nm) photon flux. Compared with that of the control, the Rd environment promoted extension growth in C. carpatica (by 65%), C. ×grandiflora (by 26%), P. sativum (by 23%), and V. ×wittrockiana (by 31%). The FRd environment suppressed extension growth in C. ×grandiflora (by 21%), P. sativum (by 17%), and V. ×wittrockiana (by 14%). Independent of the R: FR ratio, the Bd environment promoted stem extension (by 10% to 100%) in all species, but there was little or no effect on flowering percentage and time to flower. Extension growth was generally linearly related to the incident wide band (100 nm) R: FR ratio or estimated phytochrome photoequilibrium except when B light was specifically reduced. A high R: FR ratio (i.e., under the FRd filter) delayed flower initiation (but not development) in C. carpatica and C.×grandiflora and inhibited flower development (but not initiation) in V.×wittrockiana. Therefore, B light and the R: FR ratio independently regulate extension growth by varying magnitudes in LDP, and in some species, an FRd environment can suppress flower initiation or development.

The effectiveness of cool-white fluorescent, high-pressure sodium, incandescent, and metal halide lamps for inducing flowering through daylength extensions in Campanula carpatica Jacq. `Blue Clips', Coreopsis grandiflora Hogg ex Sweet `Early Sunrise', and Coreopsis verticillata L. `Moonbeam' was compared. Lighting was delivered as a 7-hour day extension with photosynthetic photon flux (PPF) ranging from 0.05 to 2.0 μmol·m-2·s-1 following a 9-hour natural daylength. Threshold irradiance values for flowering ranged from -2·s-1, depending on species. Saturation irradiance values for Campanula carpatica `Blue Clips' and C. grandiflora `Early Sunrise' were between 0.2 ± 0.2 and 0.7 ± 0.5 μmol·m-2·s-1, and did not differ between lamps. An irradiance of 1.0 μmol·m-2·s-1 from any lamp was adequate for flowering in Coreopsis verticillata `Moonbeam'. Time to flower at irradiances above the saturation points did not differ significantly between lamp types for all species tested. Campanula carpatica `Blue Clips' and Coreopsis grandiflora `Early Sunrise' plants had significantly longer stems under incandescent lamps than in any other treatment. Coreopsis verticillata `Moonbeam' plants grown under cool-white fluorescent lamps had stems ≈10% longer than those grown under high-pressure sodium or incandescent lamps.

To examine the effects of chilling and a limited inductive photoperiod (LIP) on flowering of Chrysanthemum superbum Bergmans ex J. Ingram `G. Marconi' and `Snow Lady', Coreopsis grandiflora Hogg `Sunray', and Coreopsis lanceolata L. `Early Sunrise', seeds were sown and plants were maintained in the greenhouse in short days (SDs) for 7 weeks, followed by 4 months of natural outdoor chilling for all plants except 10 of each cultivar, which remained in the greenhouse under SDs for the duration of the experiment. Upon return to greenhouse conditions, 10 plants of each cultivar were placed in SDs, all other chilled plants were placed in long-days (LDs) and subsequently transferred to SDs after receiving 6, 8, 10, 12, 14, 16, 18, 20, or 22 LD cycles. Ten chilled plants of each cultivar remained in LDs for the duration of the experiment. Continuous SDs without chilling resulted in 70%, 40%, 20%, and 10% flowering in `Snow Lady', `Early Sunrise', `Sunray,' and `G. Marconi', respectively. Chilling, followed by a return to continuous SDs, improved flowering in all cultivars compared to SDs without chilling. The number of LD cycles required for 100% flowering varied with cultivar. Ninety percent of the chilled `Early Sunrise' plants flowered with no LD cycles, and 100% flowering was produced by as few as six LD cycles. In `Snow Lady', 100% flowering occurred in chilled plants with no LD cycles and those receiving at least 10 LD cycles. With only six or eight LD cycles, 90% and 80% of these plants, respectively, still flowered. The percentage of `G. Marconi' and `Sunray' plants flowering ranged from 40% to 100% in the chilled treatments, with a general trend for more flowering with an increase in the number of LD inductive cycles. Continuous LDs following chilling resulted in as high or higher percent flowering than any other treatments (100% for `G. Marconi' and 90% for `Sunray'). The effects of LIP were evident in both Coreopsis cultivars but in neither Chrysanthemum superbum cultivar. There was a linear relationship between the number of LDs received and stem length at first flower in `Sunray' and `Early Sunrise'. In both cultivars, a reduction in stem elongation of about 10 cm occurred when plants received only 6 LDs compared to 22 LDs. The number of days from the start of LDs to first flower increased linearly as the number of LD cycles before the transfer back to SDs increased.

Juvenility and flowering requirements of Coreopsis grandiflora Hogg ex Sweet. `Sunray' and C. lanceolata L. `Early Sunrise' were examined by growing plants under short days (SD) and transferring them to long days (LD) upon reaching the designated true leaf stages. Neither cultivar flowered in continuous SD, and `Sunray' remained vegetative in LD. However, LD induced flowering in `Early Sunrise' plants in each leaf count treatment and the loss of juvenility was gradual, with most rapid flowering occurring when plants were transferred to LD at the 16 leaf stage. The limited inductive photoperiod (LIP) inhibited stem elongation of `Early Sunrise' plants in all LD treatments and selectively inhibited axillary flower bud development compared to plants grown in continuous LD. LIP did not affect scape length at first flower even though plant height was significantly diminished if given relatively few LD before transfer to SD. Height reduction was attributed to LIP inhibition of stem elongation with no significant loss of axillary flower bud potential.