Quantitative trait loci controlling flowering time and related traits in a Solanum lycopersicum × S. pimpinellifolium cross

Flowering time is an important factor determining early yield in tomato. However, the quantitative trait loci (QTLs) controlling flowering time and their relation to other QTLs for morphological and physiological traits have not been well studied. The aim of this study was to map the chromosomal regions controlling days to flowering (DTF) concurrently with other traits, such as the number of leaves preceding the first inflorescence (LN), length of the largest leaf (LL), number of lateral shoots (LS), fresh weight (FRW) and plant height (PH). This was undertaken using an inbred backcross population derived from a cross between the commercial cultivar Solanum lycopersicum cv. ‘M570018’ and its close wild relative S. pimpinellifolium (PI124039). S. pimpinellifolium flowers earlier than the cultivated tomato. Plants were grown in spring and summer. Composite interval mapping detected 16 QTLs for the six traits evaluated. These QTLs explained 10–42% of the individual phenotypic variation. QTLs detected in spring generally did not differ from those detected in summer. In chromosome 1, the DTF QTL was co-located with the QTLs for LL, LS and FRW, while in chromosome 3 it was co-located with the QTLs for LN, FRW (summer) and PH. One DTF QTL that was detected in chromosome 3 and conferred by the S. pimpinellifolium allele hastens flowering. The co-location of the DTF QTL with the LN QTL suggested that the DTF QTL in chromosome 3 controls the period from the vegetative to reproductive phase. Co-locations of DTF QTLs with the other traits might be pleiotropic effects of a single gene or cluster of genes via physiological relationships among traits because they were found to be highly significantly correlated.     

Quantitative trait analysis of transplanting time and other root-growth-related traits in tomato

Transplanting time is determined by factors such as the field conditions, the age of the seedlings, and the size of the container, but little information is available on the effect of the genetic background on transplanting time. Here, we examined root dry weight (RDW), shoot dry weight, root/shoot ratio (RSR), time at which 50% of the germinated seedlings have expanded cotyledons (CE50), root ball formation (RBW), the length of time from the cotyledon expansion from the first to the last germinated seedling (ES) and transplanting time (TRD) in a BC₁F₆ population derived from Solanum lycopersicum and Solanum pimpinellifolium. All traits exhibited significant correlation with each other, except for RSR, which was only significantly correlated to RDW. A total of eight additive quantitative trait loci (QTLs) were detected for the five traits, i.e., RSR, RBW, CE50, ES, and TRD. One epistatic (QTL × QTL) interaction each was identified for RSR and TRD. QTLs for RSR, RBW, CE50, ES and TRD clustered near marker LEOH37 on chromosome 4. Clustering of ce50-4, rsr4, rbw4, and es4 with trd4 reflected the dependence of transplanting time on root ball formation, growth uniformity and early seedling growth, especially root growth. In addition, several QTLs in this study were mapped to regions where QTLs for days to flowering or number of leaves before the first inflorescence had been identified previously. This suggests that the roots may exert some influence on the flowering time in tomato.     

Responses of Alstroemeria ‘Regina’ to temperature treatments prior to flower-inducing temperatures

Days to flower (DTF) were inversely related to the number of weeks (0–8) that Alstroemeria ‘Regina’ plants remained at 5°C, a vernalizing temperature, before being moved to 13°C, a vernalizing as well as a forcing temperature. However, when the number of weeks at 5°C was added to the DTF, no difference in the total time to flower was observed between plants treated at 5°C or those grown continuously at 13°C, as they both induced flowering. One-year-old plants maintained at 21°C, a non-inductive temperature, and not divided prior to the 5°C treatments, showed an increase in total shoot production, and delayed DTF, compared to plants which were divided. When divided plants were maintained for 16 weeks at 21°C prior to 5°C treatments, total shoot production was reduced but flowering was accelerated compared to plants maintained for 8 weeks at 21°C after dividing. Total shoot and flowering-shoot production was not affected by increasing the durations of time at 5°C when plants were grown at 21°C and divided prior to this treatment. Thus, the pre-treatment of dividing or maintaining plants at 21°C prior to a 5°C treatment affected subsequent shoot production and DTF.     

Plant growth regulators and flowering of Brunonia and Calandrinia sp.

Brunonia australis R. Br (Goodeniaceae) and Calandrinia (Portulacaceae), native to Australia, are potential new flowering potted plants. This research investigated the role of daylength and growth regulators, Gibberellic acid (GA₃) and paclobutrazol (Pac), to control vegetative growth, peduncle elongation and flowering of Brunonia and Calandrinia. Plants were grown under long days (16 h), short days (11 h) and 8 weeks under short day then transferred to long day (SDLDs). Plants in each daylength were treated with GA₃, Pac, and GA₃+ Pac. GA₃ was applied as 10 μL drop of 500 mg L⁻¹ concentration to the newest mature leaf. A single application of Pac was applied as a soil drench at 0.25 mg a.i. dose per plant. Both Brunonia and Calandrinia flowered earlier in long days but still flowered in short days, so both can be classified as facultative LD plants. Brunonia under SDLDs were more vigorous and attractive than plants under LDs while still being more compact than plants under SDs. In Brunonia, GA₃ promoted earlier flowering and increased the number of inflorescences under SDs. Pac at 0.25 mg a.i. per plant applied alone or in combination with GA₃ had extended flower development in Brunonia, and resulted in a reduced number of inflorescences per plant compared to the control plants. Vegetative growth of Calandrinia was similar under LDs, SDs and SDLDs, whereas GA₃ application increased plant size. Pac-treated Calandrinia looked compact and attractive, and Pac application did not affect time to flower and flower number.     

Deferring flowering of nobile dendrobium hybrids by holding plants under low temperature after vernalization

Orchids are currently the most valuable potted crop in the United States. To date, no studies focused on making possible the year-round greenhouse production of flowering nobile dendrobium orchids. This experiment was aimed at developing a strategy to defer flowering of nobile dendrobium orchids by holding them under low temperature. Mature Den. Red Emperor ‘Prince’ and Den. Sea Mary ‘Snow King’ were held at 10 °C for various durations (0, 4, 8, 12 or 16 weeks) after vernalization (4 weeks at 10 °C). Plants were forced in a greenhouse after holding. Time to flower, flower differentiation (flowering node percentage, number of aerial shoot and aborted bud) and flower quality (total flower number, flower diameter, flower number per flowering node and flower longevity) were determined. Increase of low temperature holding duration from 0 to 16 weeks extended time to flower up to 3 months and did not affect parameters of flower except producing larger flowers and reducing flower number per flowering node for Den. Red Emperor ‘Prince’. Notably, the flower longevity was not adversely affected. Defoliation was aggravated in Den. Red Emperor ‘Prince’ by longer duration of cooling and was considered a detrimental effect of low temperature holding.     

KClO3 applications affect Phalaenopsis orchid flowering

Potassium chlorate (KClO₃) treatments are known to promote flowering in longan plants. Potential effects of KClO₃ on Phalaenopsis orchid flowering were investigated in the present study. However, increasing application concentrations of 2, 4, 8 and 16 mmol/L KClO₃ delayed spike emergence by 5, 6, 18 and 26 days, respectively. Moreover, they reduced final spike length by 2.1%, 4.0%, 16.2% and 46.1%, respectively. Nonetheless, application of KClO₃ at 4 and 8 mmol/L advanced the time to appearance of the first open flower by 13 and 24 days, respectively. Use of 8 mmol/L KClO₃ also increased the number of floral buds by 16%. Treatments with KClO₃ tended to reduce flower size. Overall, the data suggest that application of KClO₃ at an appropriate concentration (e.g. 8 mmol/L) can increase the number of floral buds and advance the time to Phalaenopsis orchid flowering, but may reduce flower size.     

Effect of photoperiod and light integral on flowering and growth of Eustoma grandiflorum (Raf.) Shinn.

The aim of the study was to examine the effects of different photoperiod and light integral on floral initiation, development and subsequent growth of Eustoma grandiflorum (Raf.) Shinn. Six-weeks-old seedlings of ‘Echo Blue’ and ‘Fuji Deep Blue’ were placed under short day (SD, 10 h) and were transferred to long days (LD, 20 h) at 2-week intervals from 6 to 14 weeks after seeding. Plants initiated flower buds regardless of light regimes. Flower bud initiation was delayed by SD compared to LD; plants transferred after 6 weeks from seeding initiated flower buds at least 21 and 10 days earlier at LD at high (HL) and low (LL) daily light integral, respectively, compared to those at SD. Light regimes had little or no effect on time to flower bud development after initiation. Thus, it seems likely that LD and HL affected the initiation rather than development. Both the photoperiod and light integral strongly influenced the subsequent growth after initiation. SD delayed the time to visible bud (VB), increased the number of nodes to first open flower, number of branches, stem diameter and shoot dry weight compared to LD. HL promoted flowering and increased several shoot characteristics and flowering compared to LL.The results indicate that Eustoma is a quantitative long-day plant. LD, and more specifically HL, enhanced flower bud initiation, development and subsequent growth. An initial SD period is preferred to increase the number of branches, number of flowering buds and flowers, stem diameter and shoot dry weight.     

Flowering induction of Guzmania by ethylene

Ethylene exposure time required to induce flowering of Guzmania lingulata Mez. ‘Anita’ was investigated by exposing plants to ethylene at 100 μl l⁻¹ for 4, 6, 8, 10, 12, 16, or 24 h. Plants were also exposed to ethylene-free air for the same lengths of time. Plants exposed to ethylene for 4 h did not flower, but exposure for 6 h or longer resulted in 100% flowering. Suppression of endogenous ethylene synthesis by aminoethoxyvinylglycine (AVG) resulted in a longer exposure time of 20 h being required to obtain 100% flowering. This result suggests that endogenous ethylene production contributes substantially to floral induction. Ethylene treatment on a single young leaf induced flowering as well. Application of a protein synthesis inhibitor, cycloheximide, prevented flowering induced by ethylene, indicating that activation of ethylene responsive genes is followed by synthesis of new proteins involved in flowering.     

Growth and flowering of black iris (Iris nigricans Dinsm.) following treatment with plant growth regulators

The effects of application method and concentration of gibberellic acid (GA₃), paclobutrazol and chlormequat on black iris performance were assessed. Plants (10 cm high, 4 ± 1 leaves) were sprayed with 125, 250, 375 or 500 mg L⁻¹ or drenched with 0.25, 0.5, 1 or 2 mg L⁻¹ GA₃. In a second experiment, the plants were sprayed with 100, 250, 500 or 1000 mg L⁻¹ or drenched with 0.25, 0.5, 1 or 2 mg L⁻¹ paclobutrazol. Other plants were sprayed with 250, 500, 1000 or 1500 mg L⁻¹ or drenched with 100, 250, 375 or 550 mg L⁻¹ chlormequat. In each experiment, the control treatment consisted of untreated plants. Results indicated that the tallest plants (37.3 cm) in the GA₃ experiment were those sprayed with 250 mg L⁻¹. The most rapid flowering (160 days after planting) occurred when a 375 mg L⁻¹ GA₃ spray was used, whereas flowering was delayed to 200 days using 1 mg L⁻¹ GA₃ drench. Drenching with 1 mg L⁻¹ GA₃ increased height of the flower stalk by 7 cm compared to the control. Though relatively slow to flower, plants drenched with 1 mg L⁻¹ GA₃ had long and rigid stalks, which were suitable as cut flowers. Number and characteristics of the sprouts were not affected by GA₃. All paclobutrazol sprays resulted in leaf falcation. A 500 or 1000 mg L⁻¹ paclobutrazol spray resulted in severe and undesirable control of plant height, drastic reduction in stalk height and weight, and delayed flowering. Plants drenched with 0.25 or 1 mg L⁻¹ paclobutrazol were suitable as pot plants. Chlormequat reduced plant height only at the highest drench concentration, which also reduced flowering to 70%. No leaf falcation was observed with GA₃ or chlormequat. Chemical names: ( ± )-(R*,R*)-beta-((4-chlorophenyl)methyl)-alpha-(1,1,-dimethylethyl)-1H-1,2,4,-triazol-1-ethanol (paclobutrazol); (2-chloroethyl) trimethylammonium chloride (chlormequat).     

Cultivation of cut flower and bulb species with saline water

The long-term effect of saline water irrigation on flower yield and quality was investigated in three herbaceous cut flower crops of commercial importance, the Emily cultivars of Japanese limonium, Trachelium caeruleum and Eustoma grandiflorum (lisianthus), and in two bulb species, Hippeastrum hybridum and Ornithogalum arabicum. Among the tested crops, limonium showed the highest resistance to salinity. Irrigation water with an electrical conductivity of up to 11.5 dS m⁻¹ had little or no effect on stem yield and length of limonium flowering stems. In Trachelium, salinity had no effect on the yield of flowering stems or the size of the inflorescence, but it markedly reduced stem weight and length. The concomitant reduction in the number of nodes to flowering was reflected in earlier flower initiation. Since delayed flower differentiation and over-elongation of Trachelium stems is a serious problem during the winter months, application of mildly saline irrigation for winter production could be used to induce earlier flower initiation and to control stem height. In lisianthus subjected to salinity from bud appearance onwards, a salinity level of 6.0 dS m⁻¹ increased stem weight and the number of flowers per stem without affecting other quality parameters. The work carried out with Trachelium and lisianthus, although limited, indicates that salinity may be used for improving the quality of some cut flowers. In contrast to its beneficial effect on the herbaceous species, salinity led to a significant reduction of bulb, leaf, and root weight of the two bulbous species, H. hybridum and O. arabicum.     

Diversity in environmental controls of flowering in Australian plants

In adapting their flowering to a particular season of the year, plants utilize a number of environmental inputs. Knowledge of these environmental controls of flowering is important for production in commercial horticulture. Such information is also relevant for assessing whether or not a species is threatened by global warming. Here, for five Australian plant species, we document ways in which the environment regulates their flowering. Spring flowering of Croweaexalata ‘Bindelong Compact’ reflects a response to increased daily light integral, these plants showing no hint of a true long day photoperiodic response. Higher temperatures not only cause earlier flowering of this Crowea cultivar but also depress flower production (5% loss per 1 °C increase). By contrast, another Crowea, ‘White Star’, flowers only if exposed to cool temperatures (15 °C) at the time of the increase in daily light integral. Thus, in commercial horticulture, synchronous and rapid flowering of Crowea will be possible by shifting plants from shade to high light conditions. In nature, light intensity will also have a major impact on flowering. By contrast, best flowering of Lechenaultia formosa in spring is a response to short photoperiods at high temperature while L. biloba prefers long days and has potentially spring to summer flowering. Whereas rising summer temperatures could have a deleterious effect on flowering of C.exalata, global warming may have little impact on L. formosa and L. biloba which flower more profusely in warmer conditions. Another spring flowering species, Verticordia chrysantha, responds both to short days and to exposure to cool temperatures so its survival could be threatened by global warming. For Calytrix fraseri its late summer flowering in nature is explained by its requirement for an exposure to long days. When combined with information previously published for Australian plants, it is clear that there are no simple generalizations to explain why a plant species flowers when it does.     

Gibberellin-mediated suppression of floral initiation in the long-day plant Rhododendron cv. Hatsugiri

In a number of woody perennial species a decrease in gibberellins concentrations in the apical meristems is required for floral initiation to occur. In Rhododendron, applied gibberellins inhibit flowering and gibberellin biosynthesis inhibitors promote flowering. However, unlike previous reports on other Rhododendron cultivars, Rhododendron cv. Hatsugiri is a faculatitive LDP. It was therefore unknown how gibberellins regulate flowering in this cultivar and if non-inductive short daylengths stimulate the productions of endogenous gibberellins to suppress flowering. By inhibiting floral initiation while not stimulating vegetative growth we found applications of GA₅ to best match the natural response of Rhododendron cv. Hatsugiri under short-day regimes. GA₅-mediated effects on flowering have previously been reported to be due to conversion to GA₆, however, GA₅ was found to be present in tissue samples at up to 0.57 ng g⁻¹ FW, while GA₆ was never found. In addition, foliar applications of [¹⁴C] GA₅ were not found to have metabolised to GA₆. In line with the hypothesis that gibberellins inhibit floral initiation in short days in Rhododendron cv. Hatsugiri, the concentration of GA₂₀, a precursor to many bioactive gibberellins, was higher in leaf tissues from plants in short days, compared to those in permissive long days when analysed using GC–MS.     

Combining ability among male sterile two-type and restorer lines of Zinnia elegans and implications for the breeding of this ornamental species

Nineteen parental lines including five male sterile A-lines (AH002A, AH003A, AH209A, S5001A, J16A) and fourteen restorers (A1-GH, A3, S5, J6, J7N, J7J, J8, J9, J10, J11, J12, J13, J14, J17) were crossed using the North Carolina II statistical method. Studies of combining ability and heritability were conducted on selected parents along with their seventy F₁ hybrids for main ornamental traits. Plant height, crown size and length of node had obvious additive genetic effects, high (>0.50) broad sense heritability and high narrow sense heritability (length of node was medium). Pedicel length showed approximately equivalent maternal and paternal additive genetic effects, high broad sense heritability and medium (0.30–0.50) narrow sense heritability. Number of whorls of ray florets across capitulum and number of branches were able to take advantage of heterosis. The relationship between general combining ability and specific combining ability in Zinnia elegans depended on materials and traits. Male sterile two-type line was pivotal in the hybridization breeding of Z. elegans. S5001A, AH002A and A1-GH, A3, J14 which performed high negative GCA effects in PH, PL, LN and type I in PH, PL, NW, LN were ideal female and male parents of potted flowering plants; AH209A, J16A and S5, J10, J17 which displayed positive GCA effects and almost type I in PH, PL, LN were ideal female and male parents of cut flowers, respectively. For potted flowering plants, AH002A × J17, AH209A × A1-GH and S5001A × J6 with high negative SCA effects in PH, PL and LN were the most promising combinations, AH002A × S5, AH003A × A3 and J16A × J6 were the subprime combinations; for cut flowers, AH209A × S5, AH209A × J17 and J16A × J17 with high positive SCA effects in PH, PL and LN were the primary combinations, AH209A × J9 and S5001A × J10 were the secondary combinations.     

Effects of day length on flowering and yield production of Salicornia and Sarcocornia species

Salicornia is a new vegetable crop that can be irrigated with highly saline water, even at salt concentrations equivalent to full-strength seawater. During leafy vegetable cultivation, the onset of the reproductive phase is an undesired phenomenon that reduces yield and quality and prevents year-round cultivation. Knowledge about the regulation of floral induction in the members of the tribe Salicornieae, however, is lacking. To establish year-round cultivation, we studied the flower induction of five Salicornia and two Sarcocornia varieties. Plants were grown under two day lengths, 13.5 h and 18 h, and harvested by a repetitive harvest regime. A 13.5-h day length prevented flower induction in the Israeli Salicornia varieties, but a longer day length was required to prevent flower induction in two species originating from more northern latitudes. The onset of the reproductive phase under suboptimal short day length conditions severely reduced vegetative growth and yields in Salicornia. In Sarcocornia, the repetitive harvest regime prevented flowering, making it a promising candidate for year-round cultivation. Irrigating the plants with full-strength seawater (electrical conductivity 48 dS m⁻¹) vs. water with moderate salinity (electrical conductivity 10 dS m⁻¹) did not change the general flowering pattern of the studied Salicornieae members.     

观赏海棠花色时序动态分布格局研究

 采用X-Rite 色差计对97 个观赏海棠品种大蕾期（S₁）、盛开期（S₂）、末花期（S₃）3 个阶 段的花色进行了测定,开展了品种群间的花色关系及时空分布规律研究,旨在为挖掘和创制海棠特异种 质和花色育种提供参考。采用Origin7.0 软件构建了观赏海棠品种群花色在CIELCH 色空间中的三维动态 分布图,结果表明：在开花进程中,各品种花色在L*（亮度）、C*（饱和度）和h*（色调角）三个维度皆 呈规律性空间分布特点和阶段性变化趋势,所有品种的L*值持续上升而C*值持续下降,L *值高而C *值低 的品种权重显著增加;在h *维度方向,h * 值呈增大趋势,分布在红色区域（h *值0 ~ 20°）的品种权重由大 蕾期的85.6%下降至末花期的52.6%,而分布在黄色区域（h *值90° ~ 110°）的品种权重由大蕾期的2.1% 上升到末花期的28.9%。采用SAS6.12 软件构建了花色聚类分析树状图,结果表明：在遗传距离2.17 和 1.69 处,97 个海棠品种可以划分为3 大色系和6 个子色系类群,即紫红色系（含紫红、暗紫红和灰紫红 3 个子色系）、粉色系（粉红和白粉2 个子色系）和白色系类群,色系/子色系类群之间具有明显不同的色 彩参数特征。3 大色系品种花色淡化程度及淡化快慢节律差异显著,在大蕾期-盛开期-末花期的开花进 程中,白色系品种呈现由紫红-白（或稍带粉）-白色先快后慢的节律快速淡化为白色,粉色系品种由 紫红-粉-淡粉（或近白色）匀速淡化,紫红色系品种（A3 除外）呈现由紫红-紫红-淡紫红先慢后快 的节律淡化,总淡化程度显著低于粉花色系。在6 个子色系中,色彩稳定性最强的是暗紫红子色系（A2） 和紫红子色系（A1-1）,始终保持较高的饱和度,而粉花子色系色彩稳定性则逊色得多。     

Flowering and changes in respiration in Asiatic hybrid lilies as influenced by bulb vernalization

Asiatic hybrid lilies, Lilium × elegans Thunb., ‘Red Carpet’ and ‘Sunray’ were used to investigate the effect of bulb vernalization at 2.5 °C on plant growth, flowering, and CO₂ production (respiration), and to use the CO₂ production pattern to monitor the time of flower bud initiation and development. Lily shoot emergence and flowering were accelerated when bulbs received 2.5 °C bulb vernalization; however, flowering was delayed when bulbs were stored at 20 °C before treatment at 2.5 °C; this indicated that bulbs were de-vernalized. The maximum CO₂ level, and the minimum level, reached in 78 h in non-vernalized bulbs and in 110 h in 6 weeks of 2.5 °C (6 weeks/2.5 °C) treated bulbs, was increased as the 2.5 °C duration was increased; this indicated that CO₂ level can be an useful parameter to measure the cold stimulus (i) accumulated in bulbs following bulb vernalization. The respiration rate higher than the predicted values of the best-fit curves derived from the quadratic equations was designated as Blip A and this was correlated to the time of flower bud initiation and development. Shoot elongation may follow the rise in carbon dioxide levels after reaching the minimum level. It is proposed that increased carbon dioxide levels higher than the predicted levels (Blip A), was correlated to the time of flower bud initiation and development. Measurement of carbon dioxide production upon receipt of bulbs may be a useful technique to provide important information for optimum vernalization treatments for bulbs that have accumulated different levels of low temperature stimulus after bulb vernalization.     

Flowering of Primula malacoides in response to photoperiod and temperature

Primula malacoides Franch. ‘Prima Lilac’ was grown at 16 or 20 °C in combination with short days (SD, 8 h) or long days (LD, 16 h). In addition to uninterrupted growing conditions, plants within each temperature were moved at weekly intervals to the other photoperiod and left until termination. Temperature, but not photoperiod, significantly affected the rate of development from start of treatments (51 days from seeding) to 2 mm visible flower bud (VB). At 16 °C, VB averaged 30 days and at 20 °C, 48 days. Time to flower (first horizontal petals) at 16 °C increased from 56 to 64 days as SD increased from 1 week to continuous conditions while LD decreased time to flower from 64 to 56 days. Time to flower at 20 °C varied from 73 to 87 days with additional SD exposure resulting in slower and LD in faster flowering. These observations of the flowering response in ‘Prima’ are contrary to the photoperiodic classification of P. malacoides as a SD plant.     

Vernalization promotes flowering of a heat tolerant Calandrinia while long days replace vernalization for early flowering of Brunonia

The flowering responses of Brunonia australis (blue pincushion) and Calandrinia sp. to vernalization, photoperiod, temperature and plant age were investigated to provide a foundation for manipulating flowering in these potential potted plants. Plants were vernalized at 4.8 °C for 0, 3 or 6 weeks at the plant age of 1–4 or 8–14 leaves. Following vernalization, plants were grown at 25/10 or 35/20 °C (day/night) under short days (11 h, ambient daylight averaged 380 ± 44 μmol m⁻² s⁻¹) or long days (16 h) provided by an additional 5 h night break (21:00–2:00 h at <4.5 μmol m⁻² s⁻¹ from incandescent lamps), for 85 days. This is the first work to investigate flowering of these ornamental species. Both species showed enhanced flowering following vernalization and a quantitative requirement for long days. The reduction of the time until the first visible inflorescence (Brunonia) or flower (Calandrinia) buds by 8–13 days was affected by vernalization for 3 or 6 weeks, respectively. Long days were effective for reducing the time to first visible floral bud and increasing the number of inflorescence or flowers per plant for both species. For Brunonia, LDs replaced vernalization when applied to plants with 1–4 leaves. Raising temperature from 25/10 to 35/20 °C increased the number of flowers per plant of Calandrinia by 2–2.5-fold for plants with 1–4 or 8–14 leaves respectively.