Duration of cycle and injuries due to heat and chilling in gladiolus as a function of planting dates

Duração do ciclo e danos por altas e baixas temperaturas em gladíolo em função da época de plantio

ABSTRACT

The planting date is an important factor affecting the developmental cycle and quality of final product. Indications from the literature are that gladiolus is a species that can be cultivated throughout the year, but in some periods, adverse conditions may occur, reducing the quality of the flower. Two field experiments (Experiment 1: August 2011 to July 2012 and Experiment 2: August 2012 to July 2013) were conducted in Santa Maria, RS, Brazil, to quantify the influence of planting dates on the duration of the developmental cycle and on the quality of flower stems in gladiolus, identifying possible damages by high and low temperatures in the final product. It is concluded that it is possible to cultivate gladiolus throughout the year, but the duration of gladiolus cycle is higher when planting is carried out in periods of low temperatures, and this is important for scheduling the planting date, mainly for meeting specific market demand (commemorative dates). Extreme temperatures (above 35 °C and below 0 °C) reduce the commercial flowers quality and even cause the death of plants.

Keywords:
Gladiolus x grandiflorus Hort.; development cycle; extreme temperatures; frost

RESUMO

A época de plantio escolhida para cultivar uma espécie é fator determinante na duração do ciclo de desenvolvimento e na qualidade do produto colhido. O gladíolo é uma espécie que pode ser cultivada ao longo do ano, porém, em alguns períodos poderão ocorrer condições adversas ao cultivo, reduzindo sua qualidade. Foram conduzidos dois experimentos de campo em Santa Maria, RS, (Experimento 1: de agosto de 2011 a julho de 2012 e Experimento 2: de agosto de 2012 a julho de 2013) a fim de quantificar a influência da época de plantio na duração do ciclo e na qualidade das hastes de gladíolo, identificando possíveis danos por altas e baixas temperaturas no produto final. Conclui-se que é possível cultivar gladíolo ao longo do ano, porém a duração do ciclo de desenvolvimento do gladíolo é maior quando o plantio é realizado em períodos de baixas temperaturas, sendo esse dado importante para a programação da data de plantio, especialmente quando se desejar colher em datas pontuais (datas comemorativas). Temperaturas extremas (acima de 35 °C e abaixo de 0 °C) reduzem a qualidade comercial das hastes e até mesmo causam a morte da planta.

Palavras-chave:
Gladiolus x grandiflorus Hort.; ciclo de desenvolvimento; temperaturas extremas; geada

1. INTRODUCTION

Gladiolus (Gladiolus x grandiflorus Hort.) is an important cut flower in several countries worldwide (CHOUDHARY et al., 2011; AHMAD et al., 2011). In Brazil its commercial importance is mainly for All Soul's day holiday (SCHWAB et al. 2014), but its demand is starting to expand for other commemorative dates such as Mother's Day and Christmas, as well as for the ornamentation of social events. In 1976, a series of published articles on gladiolus indicated that environmental factors, such as light intensity, day length, air temperature and soil moisture, affect the growth and development of gladiolus (SHILLO and HALEVY 1976 a,b,c,d) and therefore the planting date would play an important role in regulating the crop developmental cycle (ZUBAIR et al. 2006; AHMAD et al. 2011; AKPINAR and BULUT, 2011).

Planting date is a determining factor in the duration of the developmental cycle and the quality of cut flowers, which consequently affects the scheduling of the harvest (SCHWAB et al., 2017). The scheduling of harvest is especially important for flower crops, which have a marketing calendar concentrated mainly on commemorative dates. For chrysanthemum, Nardi et al. (2000) reported that the development of plants differs according to the growing season; for “mal-me-quer-do-campo” (Aspilia montevidensis Spreng.), Fagundes et al. (2010) demonstrated that the duration of the developmental phases varies according to the growing season.

According to Barbosa et al. (2011), gladiolus can be cultivated throughout the year. However, in some periods adverse conditions may occur, mainly if there is a reduction in light and temperature, causing, according to Severino (2007), delay in harvesting, small plants, dry stems or stems with low number of buttons and decrease of the quality of floral stems.

Therefore, the objectives of this study were to quantify the influence of planting date on the duration of developmental cycle and on the quality of the gladiolus stems, identifying possible damages by high and low temperatures.

2. MATERIAL AND METHODS

Two field experiments (Experiment 1: August 2011 to July 2012 and Experiment 2: August 2012 to July 2013) were conducted with gladiolus in Santa Maria, Rio Grande do Sul State, Brazil. The experimental design was a complete block randomized with four replications, and each replication is a plot of 10 plants. Factor A was composed of three gladiolus cultivars (Peter Pears, Rose Friendship and Jester for Experiment 1, and cultivars Amsterdam, Rose Friendship and Jester for Experiment 2). During the experiment, the cultivar Peter Pears was replaced by the cultivar Amsterdam because the supply of the corms by the company was interrupted. Factor B was composed by 12 planting dates (dd/mm/yy): planting dates in Experiment 1 were 05/08/11, 02/09/11, 03/10/11, 01/11/11, 01/12/11, 04/01/12, 01/02/12, 07/03/12, 02/04/12, 02/05/12, 01/06/12, and 02/07/12, and planting dates in Experiment 2 were 02/08/12, 03/09/12, 04/10/12, 01/11/12, 03/12/12, 04/01/13, 01/02/13, 01/03/13, 01/04/13, 01/05/13, 03/06/13 and 02/07/13.

In each planting date, vernalized gladiolus corms were used, ranging in size from 0.14 to 0.16 m in circumference, which was planted in beds with 1.0 m wide, 17.0 m long and 0.1 m high, containing two paired lines, spaced 0.40 m, and plants spaced 0.20 m in the line. The blocks were set in the beds and spaced 1.0 m apart. The gladiolus water demand was supplied through drip irrigation installed on the beds. Each planting date constituted a bed.

Six plants in each block were evaluated. On these plants, the developmental stages (VE, Vn, R1.0, R1.1, R1.2, R2, R3, R3.4, R3.5, R3.6, R4, and R5), based on Schwab et al. (2015a) phenological scale, were observed daily. Data were averaged for the 24 plants of each cultivar, in each of the planting dates. Minimum and maximum daily air temperatures were measured in the automatic meteorological station of the Brazilian National Institute of Meteorology (INMET) located approximately 150.0 m from the experimental site.

In addition to phenology, daily evaluations were made about the visual aspects of stem quality (VEILING HOLAMBRA, 2018), such as sunburn stains (high temperatures) or chilling (low temperatures). The occurrence of these visual defects was correlated with air temperature, in order to indicate suitable temperatures for the gladiolus cultivation, without aesthetic damages on the stems.

3. RESULTS AND DISCUSSION

The gladiolus plants were exposed throughout Experiments 1 and 2 to a wide variation of the air temperature (Table 1). The absolute minimum air temperature was −2 °C for Experiment 1, and −0.8 °C for Experiment 2. The absolute maximum temperature was 39 °C and 39.2 °C for Experiments 1 and 2, respectively.

Table 1
Minimum and Maximum air temperature during the experimental period, in °C, (absolute, mean and standard deviation - SD) for two field experiments with gladiolus in Santa Maria, RS, Brazil.

Experiment	Planting Date		Minimum air temperature (Tmin)			Maximum air temperature (Tmax)
			Absolute	Mean	SD	Absolute	Mean	SD
1	1	05/08/2011	1.00	10.50	3.83	31.80	19.89	4.71
	2	02/09/2011	3.20	11.06	3.55	36.00	23.49	3.63
	3	03/10/2011	9.00	14.37	2.26	34.20	25.17	2.87
	4	01/11/2011	10.80	16.43	2.25	36.40	28.98	3.21
	5	01/12/2011	9.00	17.37	2.00	39.00	30.29	2.65
	6	04/01/2012	15.60	19.40	1.92	38.20	32.99	2.86
	7	01/02/2012	13.20	21.20	2.38	39.00	33.09	2.51
	8	07/03/2012	6.40	17.02	3.48	37.60	30.32	3.91
	9	02/04/2012	6.40	13.67	3.22	35.60	25.47	4.72
	10	02/05/2012	4.00	11.89	2.66	30.60	24.86	2.83
	11	01/06/2012	-2.00	9.83	4.75	31.00	19.81	5.01
	12	02/07/2012	-0.40	7.59	4.34	30.20	18.18	4.11
2	1	02/08/2012	7.00	14.95	3.52	32.20	25.41	3.97
	2	03/09/2012	3.60	13.07	3.48	33.60	23.54	3.39
	3	04/10/2012	11.80	16.74	2.41	32.20	25.70	2.40
	4	01/11/2012	12.80	17.48	2.30	35.60	30.39	2.60
	5	03/12/2012	14.60	19.90	2.15	38.20	31.14	3.32
	6	04/01/2013	11.60	18.16	2.24	37.00	30.27	2.20
	7	01/02/2013	10.20	19.09	2.63	39.20	29.87	2.09
	8	01/03/2013	11.20	16.41	2.21	32.60	26.62	2.57
	9	01/04/2013	7.00	14.43	3.26	31.40	26.39	2.01
	10	01/05/2013	1.20	10.99	3.56	31.00	21.37	3.84
	11	03/06/2013	3.80	9.49	2.34	25.00	18.90	2.37
	12	02/07/2013	-0.80	8.74	4.73	29.00	20.01	4.86

The number of days after planting (DAP) to complete each developmental stage, according to the phenological scale of Schwab et al. (2015a), pooling all cultivars and planting dates in Experiments 1 and 2, is presented in Figure 1. The lowest amplitude of variation in the duration of the stages was found for the VE stage (emergency), with a difference of 33 days between the minimum and maximum values of DAP for the occurrence of this stage. The largest amplitude was 66 days for the R4 (corolla of the last floret with visible anthers) and R5 (complete senescence of the floral stem) stages. One possible explanation for this results is that during the VE stage, development is less dependent on the variation of above ground environmental conditions, mainly air temperature, because its development occurs below ground where daily temperature variation is lower than in air temperature and, therefore, the time interval for the occurrence of this stage becomes less variable between the different planting dates than when compared to the reproductive stages of the plant, when the plant organs (leaves, stem, and florets) are directly exposed to air temperature and solar radiation. Muttoni et al. (2017) when studying the influence of air temperature on the emergence of gladiolus corms, determined the basal temperature for this phase is 5 °C. Observing Table 1, in neither of the planting dates the minimum air temperature average was below 5 °C, which, therefore, justifies the lower variation of the values found in the VE stage between the planting dates tested.

Figure 1
Variation in days after planting (DAP) to complete several developmental stages of gladiolus cultivars Jester, Peter Pears, Rose Friendship, and Amsterdam. Data of different planting dates in Experiment 1 and Experiment 2 are polled. Santa Maria, RS, Brazil.

The duration of the developmental phase (in days) from planting date (PL) to the R2 stage (when the first three florets at the bottom of the spike show the color of the corolla), considered as the harvest point of gladiolus, is presented in Table 2. For the PL-R2, there was an increase in the length of the crop developmental cycle when agrown in the coldest periods of the year (May, June, July and August plantings), compared to those cultivated in the warmer months (Table 2). These results agree with Uhlmann et al. (2017), who found a shortening of the gladiolus development cycle with the delay of the planting date from July to September for the conditions of three locations in the state of Rio Grande do Sul and with the results of Shillo and Halevy (1976c) which state that when grown in summer, the gladiolus flowers in a shorter time interval than when grown in the winter.

Table 2
The duration (in days) of the PL (planting) to the R2 (first three florets at the bottom of the spike show the color of the corolla) stage for gladiolus cultivars in Experiments 1 and 2 in Santa Maria, RS, Brazil.

Experiment	Planting date		Duration of PL-R2 (in days)
			Peter Pears	Jester	Rose Friendship
1	1	05/08/2011	95 Ab	96 Ab	95 Aab
	2	02/09/2011	77 Bc	78 Bcd	82 Acd
	3	03/10/2011	68 Cd	72 Bde	76 Ad
	4	01/11/2011	69 Bd	72 Bde	80 Ad
	5	01/12/2011	62 Bd	65 Be	73 Ad
	6	04/01/2012	66 Bd	74 Ad	77 Ad
	7	01/02/2012	69 Ad	73 Ade	*
	8	07/03/2012	*	83 Ac	76 Bd
	9	02/04/2012	**	**	**
	10	02/05/2012	*	112 Aa	102 Ba
	11	01/06/2012	103 Aa	112 Aa	98 Aab
	12	02/07/2012	99 Aab	105 Aa	90 Abc
2			Amsterdam	Jester	Rose Friendship
	1	02/08/2012	84 Abc	88Ade	87Abc
	2	03/09/2012	76 Bc	85Aefg	85Ac
	3	04/10/2012	87 Abc	79Afg	84Acd
	4	01/11/2012	75 Bc	96Ac	84ABbc
	5	03/12/2012	84Abc	92Acd	*
	6	04/01/2013	70Bc	87Adef	82Acd
	7	01/02/2013	69Bc	79Ag	76Ade
	8	01/03/2013	72Bc	89Ade	70Be
	9	01/04/2013	88Babc	98Ac	80Ccd
	10	01/05/2013	99Bab	112Ab	94Bab
	11	03/06/2013	104Ba	123Aa	99Ca
	12	02/07/2013	99Bab	109Ab	95Ca

• ^*
  Plots lost due to diseases in corms.
• ^**
  Development stopped by frost.
  Means followed by the same capital letter in the row and means followed by the same lowercase letter in the column do not differ statistically by the Tukey Test at 5%.

For Experiment 1, the increase in the length of the PL-R2 phase was 42, 48 and 28 days in the colder months for the cultivars Peter Pears, Jester and, Rose Friendship, respectively (Table 2); in Experiment 2 the increase was 35, 45 and 28 days for the cultivars Amsterdam, Jester and Rose Friendship (Table 2). The duration of the PL-R2 phase is an important indicator for farmers, since planting date planning should consider the harvest date, which is usually timely and intended for a specific event (commemorative dates) (SCHWAB et al., 2017), as the All Souls’ Day holiday.

Figures 2 and 3 show the duration of the different developmental phases of gladiolus: PL-VE (from planting to emergence); VE-R1.0 (from emergence to the beginning of the heading, which represents the vegetative phase); R1.0-R3 (from the beginning of the heading to the beginning of the anthesis); and R3-R5 (from the beginning of the anthesis to the complete senescence of the floral stem). Variations in the duration of developmental phase among cultivars in the same planting date are due to genotype characteristics, such as that found by Uhlmann et al. (2017), who classified the cultivars White Friendship, Purple Flora, Rose Friendship and Amsterdam as the earliest cultivars, and the cultivar Gold Field as the latest. The variations observed for the same cultivar during the different planting dates are the result of different meteorological conditions (Table 1) to which they were exposed, as discussed previously.

Figure 2
Duration of developmental phases (in days) for three gladiolus cultivars (Rose Friendship, Jester, and Peter Pears) in 12 planting dates (Experiment 1): PL-VE (planting - emergence); VE-R1.0 (emergency - beginning of heading); R1.0-R3 (beginning of heading - beginning of anthesis) and R3-R5 (beginning of anthesis - senescence of floral stem). Santa Maria, RS, Brazil.

Figure 3
Duration of developmental phases (in days) for three gladiolus cultivars (Rose Friendship, Jester, and Amsterdam) in different planting dates (Experiment 2): PL-VE (planting - emergence); VE-R1.0 (emergency - beginning of heading); R1.0-R3 (beginning of heading - beginning of anthesis) and R3-R5 (beginning of anthesis - senescence of floral stem). Santa Maria, RS, Brazil.

In Experiment 1 (Figure 2), it was verified that the cultivar Peter Pears had the shortest duration of all developmental phases in the 01/12/11 planting date, totaling 6 days for PL-VE; 48 days for VE-R1.0 and 10 days for R3-R5. An exception occurred for the R1.0-R3 phase, which was shorter in planting date on 04/01/12, totaling 7 days for R1.0-R3. The highest duration of the developmental phases was in the 01/06/12 planting date, except for the PL-VE phase, which occurred in the 02/07/12 planting date, totaling 28 days for PL-VE; 72 days for VE-R1.0; 13 days for R1.0-R3 and 18 days for R3-R5. Thus, it is evident that planting in high air temperatures dates (December and January) results in the shortening of the phenological phases when compared to plantings at dates with lower air temperatures (June and July) (UHLMANN et al., 2017).

For the cultivar Jester, in Experiment 1 (Figure 2), the lowest duration for the developmental phases was obtained at the 01/12/11 planting date, totaling 8 days for PL-VE; 50 days for VE-R1.0; 10 days for R1.0-R3 and 11 days for R3-R5. Duration of PL-VE of 8 days was also observed in the planting dates in January and February (planting dates 6 and 7, respectively). The lengthening of the phases occurred in the 02/05/12 and 01/06/12 planting dates, (planting dates 10 and 11, respectively), was 39 days for PL-VE (planting date 11), 67 days for VE-R1.0 (planting date 10), and 17 days for R1.0-R3 and R3-R5.

For Rose Friendship, also in Experiment 1 (Figure 2), the lowest duration of the PL-VE phase was 8 days (planting dates 5 and 6); for VE-R1.0 it was 50 days (planting date 8); for R1.0-R3 it was 9 days (planting date 6) and for R3-R5 it was 10 days (planting date 5). The longest duration of the PL-VE phase was in planting date 11 (01/06/12), totaling 25 days; for VE-R1.0, was found in planting date 10 (02/05/12), totaling 72 days; for R1.0-R3 was in planting date 8, totaling 16 days; for R3-R5 was in planting dates 2 and 3 (02/09/11 and 03/10/11, respectively), totaling 19 days. In the case of Rose Friendship, in Experiment 1, the influence of planting dates on the duration of the developmental phases is not as clear as for the cultivars Peter Pears and Jester, as presented above, probably because Rose Friendship is as an early-cycle cultivar, different from Peter Pears and Jester, which have a longer cycle.

Figure 3 shows the duration of the developmental phases in Experiment 2 for cultivars Jester, Rose Friendship, and Amsterdam. The lowest duration of PL-VE was 7 days (for Rose Friendship, planted on 04/01/2013), for VE-R1.0 it was 45 days (for Jester, planted on 04/10/2012, and Amsterdam planted on 04/01/2013); for R1.0-R3 it was 5 days (for Rose Friendship, planted on 03/06/2013); and for R3-R5 it was 10 days (for Jester, planted on 01/11/2012). The longest duration for PL-VE was 31 days (for Jester, planted on 03/12/2012); for VE-R1.0 it was 81 days (for Jester, planted on 03/06/2013); for R1.0-R3 was 24 days (for Jester, planted on 01/05/2013); and for R3-R5 it was 26 days (for Rose Friendship, planted on 03/06/2013, and Amsterdam planted on 04/10/2012).

On 09 November 2011, the first strong heat wave was recorded during the Experiment 1 (Figure 4) and injuries due to high air temperatures (36.2 °C) on the gladiolus plants were observed. Injuries due high temperatures inlcuded temporary wilting of floral stems (Figure 5A) and burns in the sepals of the florets, mainly in the Jester cultivar (Figure 5B). Importantly, there was no visual effect caused by the high air temperature in plants that were in the vegetative phase. As the damage was observed in the reproductive organs of gladiolus (from R1), it is suggested to use artificial shading on the plants during the hottest months of the year starting at R1.

Figure 4
Minimum and maximum air temperatures during August, September, October and November 2011 (Experiment 1) in Santa Maria, RS, Brazil. Date (dd/mm/yy).

Figure 5
Injuries in gladiolus spikes caused by high air temperatures on 09 November 2011 in Santa Maria, RS, Brazil: (A) wilted floral stem, (B) burned sepals and (C) normal floral stem for comparative purposes.

The negative effects caused by high air temperature happened again during the two experiments, when daily maximum temperatures were above 35 °C, demonstrating that high air temperatures cause visual damages in gladiolus and risk of the 3-4 florets of the tip of the stem do not open (UHLMANN et al., 2017), even when kept under irrigation. These damages, depending on the degree of severity, may disqualify the floral stem for commercialization (SCHWAB et al., 2005b; VEILING HOLAMBRA, 2018). Although Shillo and Halevy (1976c) have stated that the gladiolus is extremely tolerant to high air temperatures, surviving at temperatures close to 50 °C, these authors did not present in their results a detail on visual damages in leaves and floral stems resulting from these conditions.

During the period from 07/06/2012 to 09/06/2012, a frost event occurred in Experiment 1, with a minimum air temperature of −2 °C (Figure 6). During this period, plants planted on 07/03/2012 were at stages between R1.2 to R3.6, plants planted on 02/04/2012 were at stages between VF and R1.2, plants planted on 02/05/2012 were at stages between VE to V3, and plants planted on 01/06/2012 were at stage S0 (not emerged), according to phenological scale of Schwab et al. (2015a). The damages by cold became visible from 08/06/2012, when it was possible to observe that, in all the beds (except the one planted on 01/06/2012), there were burns in the leaves of some plants, but not all leaves of these plants were reached (Figures 7A and 7B).

Figure 6
Minimum and maximum air temperatures in June 2012 (Experiment 1) in Santa Maria, RS, Brazil. Date (dd/mm/yy).

Figure 7
Damage in gladiolus caused by low air temperatures: (A) and (B) Leaves; (C) Floral stems of Jester; (D) Floral button of Rose Friendship; (E) Heading (picture registered on 18 June 2012 - ten days after a frost); (F) Heading (picture registered on 04 July 2012, twenty six days after frost). Santa Maria, RS, Brazil.

Injuries caused by frost were also observed on the flower stems of the plants planted on 07/03/2012. In Experiment 2, there was a darkening of the sepals of the cultivar Jester (Figure 7C) and, for the Rose Friendship (Figure 7D) there was discoloring of the petals, resulting in a pale pink tone, different from the natural color of the cultivar. For both cultivars, after the frost event, there was an early senescence of the open buttons and the no opening of those buttons that were closed on the date of the event, which senesced before opening. Uhlmann et al. (2017), in their model for simulating development in gladiolus, alert the possibility of the death of floral stems due to the occurrence of low air temperature (frost). Nowak et al. (1992) state that flowers of subtropical and tropical origin should not be exposed to temperatures lower than 4 °C and 7 °C, respectively, because below these temperatures chilling may occur, presenting symptoms such as flower discoloration, necrotic lesions on the petals and on the leaves, and delay in opening the floral button. Thus, the occurrence of intense frost between the stages R1.2 to R3.6 makes it impossible to commercialize gladiolus stems because of visual damage (VEILING HOLAMBRA, 2018).

The plants planted on 02/04/2012 (Experiment 1), which were between the VF (visible flag leaf) and R1.2 stages (emergence of spike completed), presented chilling on the stems. The damage started as small spots (Figure 7E) and, over the days, became more pronounced due to tissue necrosis, especially in the uppermost portion (Figure 7F), the region most exposed to frost. The damages resulted in no flowering of the stems and stop in the development of the plant. In Experiment 2 there were no intense frosts and no damage was observed, corroborating with Schwab et al. (2017), who state that the gladiolus tolerates low air temperatures, which gives the crop a good adaptation to subtropical regions (such as Southern Brazil), where the species can easily be grown during Spring and Fall (SCHWAB et al., 2015b).

4. CONCLUSIONS

The gladiolus developmental cycle is shorter when planting occurs during periods of high air temperatures (summer) and higher when planting occurs in periods of low air temperatures (winter). It is possible to grow gladiolus throughout the year, but it is limited by the high temperatures in the Summer (cause visual damages in the stems), and the low temperatures in the Winter (frosts), which in addition to causing visual damage, stop the progress of plant development, resulting in lower commercial quality. During the summer months, a practical recommendation to avoid damage to the gladiolus stems is to use artificial shading on plants.

ACKNOWLEDGMENTS

The authors are thankful to “Conselho Nacional de Desenvolvimento Científico e Tecnológico” (CNPq), “Coordenação de Aperfeiçoamento de Pessoal de Nível Superior” (Capes) and “Fundação de Amparo à Pesquisa do Estado do Rio Grande do Sul” for the scholarships.

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Publication Dates

• Publication in this collection
  Apr-Jun 2018

History

• Received
  28 Mar 2018
• Accepted
  21 June 2018