Agrociencia Uruguay

ISSN-e: 2730-5066

vol. 26, no. 2, e898, 2022

DOI: https://doi.org/10.31285/AGRO.26.898

agrociencia@fagro.edu.uy

 

Plant production

Olive reproductive phenology in a warm and humid region of Santa Catarina, Brazil

Fenología reproductiva de olivos en una región cálida y húmeda de Santa Catarina, Brasil

Fenologia reprodutiva de oliveiras em uma região quente e úmida de Santa Catarina, Brasil

Eduardo Cesar Brugnara

Empresa de Pesquisa Agropecuária e Extensão Rural de Santa Catarina (Epagri), Centro de Pesquisa para Agricultura Familiar, Chapecó, Santa Catarina, Brazil

https://orcid.org/0000-0001-9894-2714

 

Rafael Roveri Sabião

Empresa de Pesquisa Agropecuária e Extensão Rural de Santa Catarina (Epagri), Centro de Pesquisa para Agricultura Familiar, Chapecó, Santa Catarina, Brazil

https://orcid.org/0000-0003-1910-4064

 

Received: 02 July 2021

Accepted: 30 August 2022

Published: 28 September 2022

 

Corresponding author: eduardobrugnara@epagri.sc.gov.br

Abstract: Olive cultivation has been spread across Brazil subtropical regions, but yields have been variable through years and locations. The objectives of this work were to characterize the reproductive phenology and quantify some productive indexes of three olive cultivars (Arbequina, Arbosana and Koroneiki) in the warm, humid subtropical climate of western Santa Catarina, Brazil. Shoots of the three cultivars were marked and the quantitative indices of flowering and fruiting were observed periodically. At the same time, the reproductive phenology was evaluated following the BBCH scale, during three seasons, in Chapecó. Reproductive budburst varied from 0 to 32%, which resulted in a relatively low number of flowers per meter of shoot if compared to traditional growing regions, unlike fruit set rates (3.69 to 11.39%), which were similar. Compared to other regions, flowering time was early: inflorescences started to grow from end of June to mid-July, depending on the year. Then maturation was precocious as well, from the end of December to mid-March, and it was later in Koroneiki. The low flowering intensity with risk of frost damages discourages the production initiative in the region.

Keywords: Arbequina, Arbosana, flowering, fruit set, Koroneiki.

Resumen: El cultivo del olivo se ha extendido por las regiones subtropicales de Brasil, pero los rendimientos han sido variables entre años y ubicaciones. Los objetivos de este trabajo fueron caracterizar la fenología reproductiva y cuantificar algunos índices productivos de tres cultivares de olivo (Arbequina, Arbosana y Koroneiki) en el clima subtropical cálido y húmedo del oeste de Santa Catarina, Brasil. Se marcaron ramas de los tres cultivares y se observaron periódicamente los índices cuantitativos de floración y fructificación. Paralelamente, se evaluó la fenología reproductiva siguiendo la escala BBCH, durante tres temporadas en Chapecó. La brotación de yemas reproductivas varió de 0 a 32%, lo que resultó en un número relativamente bajo de flores por metro de rama en comparación con las regiones tradicionales de cultivo, a diferencia de las tasas de cuajado de frutos (3,69 a 11,39%), que fueron similares. En comparación con otras regiones, el momento de floración fue temprano: las inflorescencias comenzaron a crecer desde fines de junio hasta mediados de julio, según el año. Entonces, la maduración del fruto también fue precoz, desde fines de diciembre hasta mediados de marzo, y más tarde en Koroneiki. La baja intensidad de floración con riesgo de daños por heladas desalienta la iniciativa productiva en la región.

Palabras clave: Arbequina, Arbosana, floración, cuajado, Koroneiki.

Resumo: O cultivo da oliveira se espalhou pelas regiões subtropicais do Brasil, mas os rendimentos têm sido variáveis ao longo dos anos e locais. Os objetivos deste trabalho foram caracterizar a fenologia reprodutiva e quantificar alguns índices produtivos de três cultivares de oliveira (Arbequina, Arbosana e Koroneiki) no clima subtropical quente e úmido do oeste de Santa Catarina, Brasil. Ramos das três cultivares foram marcadas e índices quantitativos de floração e frutificação foram observados periodicamente. Paralelamente, foi avaliada a fenologia reprodutiva segundo a escala BBCH, durante três safras, em Chapecó. A brotação de gemas reprodutivas variou de zero a 32%, o que resultou em um número relativamente baixo de flores por metro de ramo se comparado às regiões tradicionais de cultivo, ao contrário das taxas de frutificação (3,69 to 11,39%) que foram semelhantes. Em comparação a outras regiões, a época de floração foi precoce: as inflorescências começaram a crescer do final de junho a meados de julho, dependendo do ano. A maturação também foi precoce, do final de dezembro a meados de março, e mais tardia em Koroneiki. A baixa intensidade de floração com risco de danos por geadas desestimula a iniciativa de produção na região.

Palavras-chave: Arbequina, Arbosana, floração, frutificação efetiva, Koroneiki.

1. Introduction

The olive tree (Olea europaea L.) has been grown in the Mediterranean region for centuries. Its cultivation has been expanded to other regions of the world, mainly between latitude 30° and 45°; regions with hot and dry summer and cold and wet winter. In lower latitudes the cold necessary for bud differentiation is conferred by altitude, allowing its cultivation(1). The species was introduced in Brazil by the Portuguese around 1800, arousing great interest in Rio Grande do Sul and Minas Gerais states. Experimental works and small plantations prior to 1979 are reported in Santa Catarina state. However, even demonstrating a high productive potential, the old plantations, maintained without adequate management techniques or the support of agricultural research in this field, were eliminated due to phytosanitary problems and gradually abandoned(2).

Olive trees grow at relatively low temperatures. In Maria da , Minas Gerais, it was estimated that the basal temperature is 10.5 to 11 ºC(3). Differences are observed between varieties in the heat requirement for growth(4), which affects their adaptation. The duration of the phenological stages depends on heat accumulation, measured in degree-days. The amount of heat (temperatures above 10 ºC) required since flowering to reach maturity is variable between varieties. For a high production of olive oil, it is ideal to accumulate 4,100 degree-days, despite in some regions maturation is reached with 1,300 degree-days(5).

The process of flower induction in olive is not well known. The initial stimulus for bud floral differentiation has been believed to occur even in the summer, during its formation in the shoot tips, a six-week long process. Some factors can affect the induction: the presence of fruits with seeds in the shoot, bud and shoot position, radiation, nutritional status and water balance(6)(7)(8). However, recent evidences of induction-related gene expression contest the summer induction theory, suggesting that it happens when trees are exposed to at least 75 days with temperatures reaching levels below 15 °C(9).

The morphological changes in the buds until the winter rest are very subtle, practically imperceptible(10). Winter temperature should ideally reach 2 to 18 ºC to promote the floral differentiation of the induced buds(11). Yet, the need for chilling hours for good floral differentiation varies across cultivars. Without a minimum chilling flowering can even occur, but in low intensity(12). In northwestern Argentina, Catamarca, La Rioja and Sumalao, at 28º latitude, similar to Santa Catarina, the occurrence of chilling is much lower than that observed in the Mediterranean region, and considered insufficient for most of the varieties(13).

The State of Santa Catarina (southern Brazil) is a favorable place for olive cultivation when considering the maximum and minimum air temperature, but marginal in terms of rainfall, which is excessive(14). Another mapping of the state with macro regional average bioclimatic indexes points out that the western region is unsuitable(15). More recently, the western Santa Catarina region was classified as risky due to insufficient chilling and frost frequency(16).

From 2008 to 2014, Koroneiki olive cultivar produced more than a thousand liters of oil per hectare per year in a trial in Santa Catarina (Caçador municipality, 1,033 m of elevation), but in Chapecó (638 m of elevation) the flowering and yield have been fickle through years(17)(18). The causes of variation have not been established, but based on the literature(16), we hypothesize insufficient chilling, and high air temperature and humidity at flowering are the most likely.

The objectives of this work were to characterize the reproductive phenology and quantify some productive indexes of 3 olive cultivars (Arbequina, Arbosana and Koroneiki) in western Santa Catarina warm, humid subtropical climate.

2. Materials and methods

The study was performed in Chapecó, Santa Catarina, Brazil, at 650 m elevation and -27.1° of latitude. The climate is subtropical with warm summers (Cfa, Köppen), and the soil is a dystrophic Red Latosol. In March, 2018, 5-year-old trees (3 ‘Arbequina’, 4 ‘Arbosana’ and 4 ‘Koroneiki’, from a collection planted in field in November, 2013) were selected, all finishing an off year (avoiding low floral intensity due to inhibition by previous season fruit), but having already flowered in previous seasons. They were spaced 6×5 m and managed with regular pesticide sprayings and fertilization, including spraying of boron previously to flowering, and pruned in an open vase shape. Tree sizes are presented in Table 1. Trees evaluated here were less than 40 m far from each other, and in this range other varieties flowered only in 2020, but in low intensity. Another olive varieties collection was sited 500 m away.

Evaluations were performed in the seasons 2018/19, 2019/20 and 2020/21. Prior to buds leaving autumn/winter rest (May to June), in each season, 120 shoots of each variety, divided equally among the plants, were selected and marked. The shoots were terminal, formed in the same growing season, with an inclination of less than 45º in relation to the horizontal, measured from 5 to 35 cm in length (Table 1), and located in the middle height of the crown. For each shoot, the length and the number of buds were registered (Table 1). The shoots were observed weekly since the last week of June to identify the beginning of inflorescence development.

Meteorological observations from automatic weather station 1041 – Epagri (Chapecó, 27,09°S/ 52,64°W, 687 m of elevation)(19) are presented in Figures 1, 2 and 3 in Supplementary material.

2.1 Flower and fruit quantity

Each shoot was observed for the number of inflorescences, flowers or fruits from beginning of inflorescence growth until harvest. Field data were used to calculate the following indexes: percentage of flowering shoots, inflorescence number per meter of shoot, percentage of reproductive budburst, number of flowers per inflorescence, and fruit set. Fruit set was calculated taking the fruit counts when the fruit drop curve stabilized (December 5, 2018; November 11, 2019; November 13, 2020), and dividing by the maximum number of flowers registered.

Table 1

Variation in tree canopy volume number of axillary buds and length of the sampled shoots measured from May to June and mass of fruit picked in ‘Arbequina’ ‘Arbosana’ and ‘Koroneiki’ olive trees in 3 seasons Chapecó Brazil

Feature

2018/19

2019/20

2020/21

- - - - - - - - - - - - - - ‘Arbequina’ - - - - - - - - - - -

Volume (m³)

8.8-11

26.3-31.2

of buds

12-50

10-46

11-47

Length (cm)

10-35

5.5-34

7.0-33

Fruit picked (kg)

<0.1

≤0.1

13.2-15.5

- - - - - - - - - - - - - - -’Arbosana’ - - - - - - - - - - -

Volume (m³)

10.2-15.0

14.7-40.9

of buds

14-52

6-48

7-44

Length (cm)

6.5-35

3.5-30

4.0-35

Fruit picked (kg)

<0.1

<0.1

1.5-12.2

- - - - - - - - - - - - - - - ‘Koroneiki’ - - - - - - - - - - -

Volume (m³)

13.1-22.4

18.5-41.2

of buds

12-40

8-46

10-34

Length (cm)

6.5-35

2.5-33

5.5-33

Fruit picked (kg)

0.3-5.0

0.02-0.4

5.8-23.9

2.2 BBCH phenological stages

Assessment of phenology was made based on the BBCH phenological scale(20), on a weekly basis at flowering and maturation phase and every two weeks at fruit growing, whenever possible. For each shoot, inflorescences were observed individually, and the predominant, the most advanced, and the most delayed stages were written down. The evaluation was completed in the harvest phase (stage 80 or more advanced).

2.3 Data analysis

Data on percentage of reproductive budburst, inflorescences per meter of shoot, fruit per inflorescence and fruit set were averaged in each tree. In each season, all parameters were submitted to analysis of variance (ANOVA, α=0.05) having cultivars as factor, in a completely random design, where the experimental unit was each individual tree (3 repetitions of ‘Arbequina’, and 4 of ‘Arbosana’ and ‘Koroneiki’). When significant, the ANOVA was complemented by a Tukey test.

3. Results

3.1 Flowering and fruiting indexes

The percentage of flowering shoots varied throughout years and cultivars (Table 2). In ‘Arbequina’ and ‘Arbosana’ it grew over the years, while in ‘Koroneiki’ it was more stable, but still reaching from 13.33 to 72.57%. In 2020/2021 94% of ‘Arbequina’ shoots flowered, while the lowest flowering shoots percentage was observed in ‘Arbosana’ in 2018/2019. Flowering shoots percentage in ‘Arbosana’ was significantly lower than in ‘Arbequina’ the last two seasons.

The percentage of reproductive budburst and inflorescence density, given as the number by meter of shoot, followed the same trend seen in the percentage of flowering shoots. The lowest values were found in ‘Arbosana’ (2018/2019) and the highest in ‘Arbequina’ (2020/2021) (Table 2). In 2018/2019 ‘Arbosana’ emitted just one inflorescence in all 120 shoots evaluated, so those data will be ignored in the rest of section 3.

Table 2

Percentage of flowering shoots and reproductive budburst, number of inflorescences per meter of shoot, number of flowers per inflorescence (FPI), and fruit set in 3 olive cultivars and growth seasons (Chapecó, Brazil)

Season

Flowering shoots

Reproductive budburst

Inflorescences per meter

FPI

Fruit set

- - - - - - - - (%) - - - - - - - -

- - - - - - - - () - - - - - - - -

(%)

2018/2019

Arbequina

14.17 nsI

0.97 ns

1.56 ns

13.81 b

4.40

Arbosana

0.83

0.03

0.30

ndIII

ndIII

Koroneiki

21.01

4.27

6.09

17.88 a

ndiv

2019/2020

Arbequina

43.33 aII

3.35 ns

5.50 ns

14.67 ns

6.28 ns

Arbosana

9.17 b

0.63

1.22

13.11

7.75

Koroneiki

15.33 ab

2.19

3.60

17.44

ndIV

2020/2021

Arbequina

94.12 a

32.54 a

53.48 a

13.36 ns

3.69 ns

Arbosana

49.17 b

6.28 b

10.25 b

13.80

11.39

Koroneiki

72.57 ab

26.14 a

38.80 ab

13.67

8.08

I Differences inside the harvest season are not significant (ANOVA, α=0.05).II Means followed by the same letter inside each harvest season are not significantly different (Tukey, α=0.05).III Not determined – absence of fruit in the tagged twigs.IV It was not feasible to determine a time to calculate it because fruit drop occurred continuously until ripening.

. Differences inside the harvest season are not significant (ANOVA, α=0.05).

II Means followed by the same letter inside each harvest season are not significantly different (Tukey, α=0.05).

III Not determined – absence of fruit in the tagged twigs.

IV It was not feasible to determine a time to calculate it because fruit drop occurred continuously until ripening.

3.2 Reproductive phenological stages

The phenological stages observed for each evaluation date and cultivar are presented in Figures 1 and 2. The earliest flower opening (BBCH 60) occurred between July 30 and August 8, 2020, in ‘Arbequina’ and ‘Koroneiki’, and between August 14 and 20, 2020, in ‘Arbosana’, which was the latest in all evaluated years (Figure 2). Opening flowers continued to be observed for a long period: in 2020, ‘Arbequina’ emitted new inflorescences from June 24 to September 25, a 93-day period. The shortest period was with ‘Koroneiki’ in 2019: 53 days. Therefore, the open-flower period (stages 60 to 68) lasted 41 to 68 days (excepting ‘Arbosana’ in 2018).

The stage 80 (deep green fruit getting light green or yellowish) was observed first in ‘Arbequina’. ‘Koroneiki’ had the last evaluated inflorescence to reach stage 80 in two seasons (Figure 1). The dates when all ‘Arbequina’ and ‘Koroneiki’ fruits reached 80 or a more advanced maturation stage were February 5, in 2019, and in 2020, January 9, 16 and 23, for ‘Arbequina’, ‘Arbosana’ and ‘Koroneiki’, respectively. In the 2020/2021 season, Arbosana's fruits were all in stage 80 still in December 23, 2020, while ‘Arbequina’ and ‘Koroneiki’ needed more time (January 8 and 15, 2021, respectively).

Occurrence of reproductive phenological stages of BBCH scale (left axis), and
percentage of flowers or fruits persistent in the shoots (right axis),
evaluated along 3 reproductive seasons in ‘Arbequina’ and ‘Koroneiki’, and 2
seasons in ‘Arbosana’ olive trees, in Chapecó, Brazil
Figure 1
Occurrence of reproductive phenological stages of BBCH scale (left axis), and percentage of flowers or fruits persistent in the shoots (right axis), evaluated along 3 reproductive seasons in ‘Arbequina’ and ‘Koroneiki’, and 2 seasons in ‘Arbosana’ olive trees, in Chapecó, Brazil

Time of flower opening light yellow and predominance of inflorescences in BBCH 65 dark yellow in ‘Arbequina’ ‘Arbosana’ and ‘Koroneiki’ olive trees in 3 years in Chapecó Brazil
Figure 2
Time of flower opening light yellow and predominance of inflorescences in BBCH 65 dark yellow in ‘Arbequina’ ‘Arbosana’ and ‘Koroneiki’ olive trees in 3 years in Chapecó Brazil

4. Discussion

Flowering shoots varied in quantity throughout years and cultivars. As the percentage of flowering shoots increased, the percentage of reproductive budburst and inflorescences by meter of shoot increased too, i. e., the floral intensity incremented. The result is a higher number of flowers emitted in a canopy volume unit, leading to bigger fruit yield (Table 1). The variation among years in the same cultivar was higher than the variation among cultivars in the same year, which suggests that climate conditions and tree age may be the main factors influencing flowering intensity.

In Chapecó and other close, similar sites, the 3 cultivars were capable of flowering(18) and fructify(17) in the third season (less than 3 years it the field). Furthermore, in the Mediterranean temperate climate of Cyprus, tree yield increases until the fourth year. From then on the yield decreases or is maintained(21). Those evidences suggest that the 5-year-old trees in Chapecó had already overcome juvenility in the start of the study. So, the inter-year variation observed in flower density is probably due to climatic conditions. This thesis is supported also by the higher counting of days with minimum temperature under 16 ºC (75, 63 and 94 in 2018, 2019, and 2020, respectively). In Greece, under Mediterranean temperate climate, a reduction in the number of flowers per ‘Koroneiki’ tree happens when chilling is reduced from 1,835 to 1,214 hours under 16 °C(22). It has been demonstrated that when ‘Arbequina’ and ‘Koroneiki’ are exposed to high temperatures (23.9 to 26.6 °C) during the chilling period the intensity of flowering is lower(23)(24). This may explain in part the low flowering intensity in Chapecó, since along May and June of 2018, 2019 and 2020 (chilling period), temperatures reached more than 23.9 °C in 25, 26 and 19 days, respectively. Using a chilling units model which discounts units as high temperatures occur, the chilling necessity of 234 units for ‘Arbequina(25) was not reached in any year. So, it can be hypothesized that insufficiency of chilling, even in the best year (2020), caused poor reproductive budburst, which is supported by the asynchrony in flower and fruit phenological stages(26) (Figure 1).

Arbosana’ flowered scarcely, irrespective of the year, which suggests it needs more chilling than ‘Arbequina’ and ‘Koroneiki’. However, there is a lack of precise information on chilling requirements of olive cultivars in general. Irrespective of the cultivar, the number of inflorescences can be considered low to intermediate if compared to other regions: in the arid Egypt the cultivars Tofahi and Aggizi average in 2 years 66 inflorescences per meter of shoot(27), which is more than all observations in Chapecó, except ‘Arbequina’ in 2020/2021; in Greece, ‘Koroneiki’ emits 60 to 80 inflorescences per meter of shoot along 3 years(28).

The cultivars, in general, had a similar number of flowers per inflorescence, compatible with the observations in another humid, subtropical region — Barra do Ribeiro, Rio Grande do Sul(29). In Spain, inflorescences of olive varieties including ‘Arbequina’ and ‘Koroneiki’ were evaluated in different environments with Mediterranean climate, showing a great variability in flower number. The environmental influence is bigger than the genetic effect(30). ‘Koroneiki’ has inflorescences with more flowers than ‘Arbequina’ in some locations of Spain. However, ‘Arbequina’ showed more than 75% of perfect flowers irrespective of the environment(31), agreeing with the superiority of ‘Arbequina’ over ‘Koroneiki’ in Barra do Ribeiro(29).

All the varieties started the sprout from June to beginning of August, depending on the season. In Uruguay, a region with humid, temperate climate, across 10 years of observation in ‘Arbequina’, the earliest sprout happened in mid-August(32). The implication of early sprouting is the risk of low, positive temperature and frost damage to inflorescences, since in Chapecó and adjacent areas frosts are expected until September(33). In addition, in Uruguay, ‘Arbequina’ flowers in a window of 52 days, shorter than in Chapecó.

The flowering time of ‘Arbequina’ and ‘Koroneiki’ was also earlier than the observed in the subtropical climate of Bagé, Brazil, (31°19’53'' S, 212 m elevation)(34), probably because in Chapecó temperatures tended to be higher during the winter, which started up inflorescence growth more precociously(35). As an example, July average temperature in the 3 years varied from 15 to 17 ºC in Chapecó, and from 10 to 12 ºC in Bagé, despite different years.

While in Chapecó full flowering occurred around the 50th day of the second semester, in colder places of Europe it takes 130(23) to 150(26) days in the equivalent semester (the first).

Flowering duration varied from 50 to 68 days (excepting ‘Arbosana’ in 2018), agreeing with observations in a subtropical climate (Canary Islands), but longer than in a typical Mediterranean climate (Andalucía)(26), and cooler places, such as Salto and Las Brujas (Uruguay), where ‘Arbequina’ flowering time lasts 6-18 and 7-28 days, respectively(32). In Canary Islands, the trees show high amplitude of phenological stages at the same date(26), similar to the observed in Chapecó (Figure 4 in Supplementary material).

Figure 2 illustrates how flowering time varied between years and cultivars. During the 3 years, the 3 cultivars flowering time overlapped in their majority, but the time when flower opening concentrated was not the same, except for ‘Arbequina’ and ‘Koroneiki’ in 2020.

Differences in full flowering date are common even in colder climates, as in Ubeda, Andalucía, where full flowering date varies even 26 days in ‘Arbequina’ between years(26). In southern Spain, ‘Arbequina’, ‘Arbosana’ and ‘Koroneiki’ under several Mediterranean environments show small differences in full flowering date. Even though it is later in ‘Arbosana’ than in ‘Arbequina’, partial coincidence of full flowering period and overall flowering period is observed among them(30). So, maybe those long and different flowering periods in Chapecó could be due to the warmer climate.

The poor synchrony among varieties can result in low pollen amounts suspended in the air the time most flowers are open, making cross-pollination less likely. This can be crucial for ‘Arbequina’, which is considered not self-compatible(36)(37). In Rio Grande do Sul, bagged ‘Arbequina’ shoots set fruits, but less than no bagged ones(29), which means it benefits from cross pollination.

In the years when fruit set was higher, tree yield was lower, and the opposite relation was observed with flowering intensity and yield (Table 1). In years with intense olive flowering, only 1 to 4% of the flowers become fruit, due to the high competition for assimilates(7). This index can reach 10%(8). In the arid Chaco, Córdoba, Argentina, 3.6% of fruit set results in more than 80 kg tree-1 of fruit (70-year-old ‘Arbequina’ trees, 10×10 m spacing)(38). In Barra do Ribeiro, fruit set is not determinant for fruiting(29). Further, during the pollination period in Chapecó, days with average air relative humidity above 80% or lower than 60% were slightly predominant (Table 3 and Figure 5 in Supplementary material), which probably did not harm pollination in a way to avoid a good fruit set. Therefore, based on the present observations, it is not possible to state that the fruit set limits the yield in Chapecó.

Table 3

Number of days with maximum air temperature higher than 25 ºC with average air relative humidity higher than 80% or lower than 60% and with pluvial precipitation in Chapecó along the olive pollination period in 3 years

Air relative humidity

Pluvial precipitation

Year

Pollination duration

>80%

<60%

- - - - - - - - - - - - - - - - - - - - - - - - - - - (days) - - - - - - - - - - - - - - - - - - - - - - - - - - -

2018

64

33

3

36

2019

65

15

21

19

2020

74

17

22

17

Olives can be picked when fruits turn deep green to yellowish green, which is equivalent to the BBCH stage 80(20). In Chapecó, the latest cultivar to reach harvest time was ‘Koroneiki’, contrasting ‘Arbequina’, in accordance with results in Croatia(39), a colder site. In Minas Gerais, in a higher altitude (1,276 m) compared to Chapecó, ‘Arbequina’ harvesting time starts on January 20 to 25(40), later than in Chapecó. The precocity in fruit maturation can be explained by the early flowering, low fruit load (which accelerates the maturation(41)), and quicker accumulation of degree-days(42) compared to colder regions.

Early harvest helps to avoid higher air humidity times in the end of summer and autumn(33), which can ease losses by anthracnose caused by Colletotrichum sp.(43). Nevertheless, a long flowering period leads to variability in fruit ripening stage in a same tree. Growers will have to wait to harvest an entire tree when almost all fruits reach a minimum maturity, when others could have reached advanced stages, which is a risk of high acidity and low polyphenol content in the oil, especially in trees with low fruit load(41). In addition, higher temperatures and solar radiation during oil synthesis and accumulation could cause an undesirable balance in oleic versus linoleic acids, and lower oil accumulation(44)(45).

5. Conclusions

When the olive cultivars Arbequina, Arbosana and Koroneiki are grown in the conditions of Chapecó, Santa Catarina, Brazil, inflorescence budburst occurs early, from end of June to end of July, flowering from early August to early November, and maturation starts from end of December until early February. In comparison to traditional olive growing regions, flowering intensity is low in some years as a direct effect of climatic conditions; nevertheless, fruit set is similar.

Although the evaluated cultivars produce fruits under Chapecó conditions, the lack or low intensity of flowering associated to sprouting in a time with risk of frosts will probably make growers to experience unstable olive harvests, sometimes null, which discourages their initiative in this region.

Acknowledgments

We thank the Fundação de Amparo à Pesquisa e Inovação do Estado de Santa Catarina for funds granted.

References

1. Villa F, Oliveira AF. Origem e expansão da oliveira na América Latina. In: Oliveira AF, editor. Oliveira no Brasil: tecnologias de produção. Belo Horizonte: EPAMIG; 2012. p. 21-38.

2. Gomes RP. A olivicultura no Brasil. 2a ed. rev. São Paulo: Nobel; 1979. 237p.

3. Martins FB, Reis DF, Pinheiro MVM. Temperatura base e filocrono em duas cultivares de oliveira. Cienc Rural. 2012;42(11):1975-81. doi:10.1590/S0103-84782012001100011.

4. Aybar VE, Abreu PM, Searles SPS, Matias AC, Río C, Caballero JM, Rousseaux MC. Evaluation of olive flowering at low latitude sites in Argentina using a chilling requirement model. Span J Agric Res. 2015;13(1):e0901. doi:10.5424/sjar/2015131-6375.

5. Tapia F, Ibacache A, Astorga M. Requerimientos de clima y suelo. In: Tapia F, Astorga A, Ibacache A, Martínez L, Siera C, Quiroz C, Larraín P, Riveros F. Manual del cultivo del olivo. La Serena: Instituto de Investigaciones Agropecuarias; 2003. p. 11-20.

6. Fabbri A, Benelli C. Flower bud induction and differentiation in olive. J Hortic Sci Biotech. 2000;75(2):131-41. doi:10.1080/14620316.2000.11511212.

7. Rallo L, Cuevas J. Fructificación y producción. In: Barranco D, Fernández-Escobar R, Rallo L. El Cultivo del Olivo. 6a ed. Madrid: Mundi-Prensa; 2008. p. 127-62.

8. Fiorino P, Marone E, Rosati A, Caporali S, Paoletti A. Il fiore e la biologia fiorale [Internet]. Spoleto: Accademia Nazionale dell’Olivo e dell’Olio; 2011 [cited 2022 Aug 31]. 17p. Available from: http://dspace.unitus.it/bitstream/2067/2597/1/au1_fiorino_etal_fiore_biologia_fiorale.pdf.

9. Haberman A, Bakhshian O, Cerezo-Medina S, Paltiel J, Adler C, Ben-Ari G, Mercado JA, Pliego-Alfaro F, Lavee S, Samach A. A possible role for flowering locus T-encoding genes in interpreting environmental and internal cues affecting olive (Olea europaea L.) flower induction. Plant Cell Environ. 2017;40(8):1263-80. doi:10.1111/pce.12922.

10. Fabbri A, Alerci L. Reproductive and vegetative bud differentiation in Olea europaea L. J Hortic Sci Biotech. 1999;74(4):522-7. doi:10.1080/14620316.1999.11511146.

11. Sibbet GS, Osgood J. Site selection and preparation, tree spacing and design, planting, and initial training. In: Sibbett GS, Ferguson L, Lindstrand M, editors. Olive production manual. 2a ed. Davis: UCANR; 2005. p. 27-34.

12. Malik SAN, Bradford JM. Is chilling a prerequisite for flowering and fruiting in ‘Arbequina’ Olives?. Int J Fruit Sci. 2005;5(3):29-39. doi:10.1300/J492v05n03_04.

13. Ayerza R, Sibbett GS. Thermal adaptability of olive (Olea europaea L.) to the Arid Chaco of Argentina. Agric Ecosyst Environ. 2001;84:277-85. doi:10.1016/S0167-8809(00)00260-7.

14. Wrege MS, Coutinho EF, Pantano AP, Jorge RO. Distribuição potencial de oliveiras no Brasil e no mundo. Rev Bras Frutic. 2015;37(3):656-66. doi:10.1590/0100-2945-174/14.

15. Thomé VMR, Zampieri S, Braga HJ, Pandolfo C, Silva Júnior VP, Bacic I, Laus Neto J, Soldateli D, Gebler E, Ore JD, Echeverria L, Mattos M, Suski PP. Zoneamento Agroecológico e Socioeconômico de Santa Catarina. Florianópolis: Epagri; 1999. CD­ROOM.

16. Pandolfo C, Brugnara EC, Ricce WS, Vianna LFN, Leite GB. Risco climático para oliveira em Santa Catarina. Agrometeoros. 2021;29(1):1-14. doi:10.31062/agrom.v29.e026930.

17. Da Croce DM, Brugnara EC, Oliveira VP, Dias CR. Avaliação da produção e do rendimento de azeite das oliveiras ‘Arbequina’, ‘Arbosana’ e ‘Koroneiki’ em Santa Catarina. RAC. 2016;29(1):54-57.

18. Bugnara EC. Crescimento, floração e frutificação de oliveiras jovens em altitude intermediária do Oeste de Santa Catarina, Brasil. RAC. 2019;32(2): 46-48.

19. Empresa de Pesquisa Agropecuária e Extensão Rural de Santa Catarina. Banco de dados de variáveis ambientais de Santa Catarina. Florianópolis: Epagri; 2020. 20p.

20. Sanz-Cortés F, Martinez-Calvo J, Badenes ML, Bleiholder H, Hack H, Yacer G, Meier V. Phenological growth stages of olive trees (Olea europaea). Ann App Biol. 2002;140(2):151-7. doi:10.1111/j.1744-7348.2002.tb00167.x.

21. Usanmaz S, Kahramanoğlu İ, Alas T, Okatan V. Performance and oil quality of seven olive cultivars under high density planting system in northern cyprus. Pak J Bot. 2019;51(5):1775-81. doi:10.30848/PJB2019-5.

22. Koubouris G, Limperaki I, Darioti M, Sergntan C. Effects of various winter chilling regimes on flowering quality indicators of Greek olive cultivars. Biol Plant. 2019;63:504-10. doi:10.32615/bp.2019.065.

23. Malik NAS, Bradford JM. The effect of high daytime temperatures on inhibition of flowering in ‘Koroneiki’ olives (Olea europaea L.) under chilling and non-chilling nighttime temperatures. J Appl Hortic. 2009;11(2):90-4. doi:10.37855/jah.2009.v11i02.18.

24. Malik NSA, Perez JL. The effect of high temperature interruptions during inductive period on the extent of flowering and on metabolic responses in olives (Olea europaea L.). Sci Hortic. 2011;129(2):207-12. doi:10.1016/j.scienta.2011.03.028.

25. De Melo-Abreu JP, Barranco D, Cordeiro AM, Tous J, Rogado BM, Villalobos FJ. Modelling olive flowering date using chilling for dormancy release and thermal time. Agric For Meteorol. 2004;125(1-2):117-27. doi:10.1016/j.agrformet.2004.02.009.

26. Medina-Alonso MG, Navas JF, Cabezas JM, Weiland CM, Ríos-Mesa D, Lorite I, León L, De la Rosa R. Differences on flowering phenology under Mediterranean and Subtropical environments for two representative olive cultivars. Environ Exp Bot. 2020;180:104239. doi:10.1016/j.envexpbot.2020.104239.

27. Ahmed ZFR. Flowering, fruiting of two table olive cultivars “Olea europaea L.” grown in Southern Egypt. Egypt J Hort. 2019;46(1):145-53. doi:10.21608/EJOH.2019.10065.1102.

28. Koubouris GC, Metzidakis IT, Vasilakakis MD. Phenological, morphological and functional indicators of genetic variability and their implication in the sexual reproductive system of Olea europaea L. (Oleaceae). Sci Hortic. 2010;123(4):547-50. doi:10.1016/j.scienta.2009.11.012.

29. Witter S, Tonietto A, Efrom CFS, Oliveira AMR, Wolff VRS, Varone F. Aspectos fitotécnicos do cultivo da oliveira no Rio Grande do Sul I: biologia reprodutiva. Pesq Agrop Gaúcha. 2019;25(3):133-45. doi:10.36812/pag.2019253133-145.

30. Navas-Lopez JF, León L, Rapoport HF, Moreno-Alías I, Lorite IJ, de la Rosa R. Genotype, environment and their interaction effects on olive tree flowering phenology and flower quality. Euphytica. 2019;215(11):1-13. doi:10.1007/s10681-019-2503-5.

31. Navas-Lopez JF, León L, Rapoport HF, Moreno-Alías I, Medina MG, Santos C, Porras R, Lorite IJ, de la Rosa R. Flowering phenology and flower quality of cultivars ‘Arbequina’, ‘Koroneiki’ and ‘Picual’ in different environments of southern Spain. Acta Hortic. 2018;(1229):257-62. doi:10.17660/ActaHortic.2018.1229.39.

32. Conde-Innamorato P, Arias-Sibillotte M, Villamil JJ, Bruzzone J, Bernaschina Y, Ferrari V, Zoppolo R, Villamil J, Leoni C. It is feasible to produce olive oil in temperate humid climate regions. Front Plant Sci. 2019;10:1544. doi:10.3389/fpls.2019.01544/full.

33. Pandolfo C, Braga HJ, Silva Júnior VP, Massignan AM, Pereira ES, Thomé VMR, Valci FV. Atlas climatológico do Estado de Santa Catarina [Internet]. Florianópolis: Epagri; 2002 [cited 2022 Aug 31]. Available from: https://ciram.epagri.sc.gov.br/index.php/solucoes/climatologia/

34. Cappellaro TH. Período de floração e viabilidade do pólen das cultivares de oliveira Arbequina e Koroneiki, em Bagé/RS [master’s thesis on Internet]. Pelotas (BR): Universidade Federal de Pelotas; 2010 [cited 2022 Aug 31]. 45p. Available from: http://guaiaca.ufpel.edu.br:8080/bitstream/123456789/2140/1/Dissertacao_Thais_Cappellaro.pdf.

35. Elloumia O, Ghraba M, Chattia A, Chaaria A, Ben Mimounb M. Phenological performance of olive tree in a warm production area of central Tunisia. Sci Hortic. 2020;259:108759. doi:10.1016/j.scienta.2019.108759.

36. Marchese A, Marra FP, Costa F, Quartararo A, Fretto S, Caruso T. An investigation of the self- and inter-incompatibility of the olive cultivars “Arbequina” and “Koroneiki” in the Mediterranean climate of Sicily. Aust J Crop Sci [Internet]. 2016 [cited 2022 Aug 31];10(1):88-93. Available from: https://www.cropj.com/marchese_10_1_2016_88_93.pdf.

37. Sánchez-Estrada A, Cuevas J. ‘Arbequina’ olive is self-incompatible. Sci Hortic. 2018;230(7):50-5. doi:10.1016/j.scienta.2017.11.018.

38. Pierantozzi P, Torres M, Bodoira R, Maestri D. Water relations, biochemical – physiological and yield responses of olive trees (Olea europaea L. cvs. Arbequina and Manzanilla) under drought stress during the pre-flowering and flowering period. Agric Water Manag. 2013;125:13-25. doi:10.1016/j.agwat.​2013.04.003.

39. Biško A, Milinović B, Vujević P, Ivanović A, Halapija Kazija D, Jelačić T, Čiček D. First results with super-high-density olive growing in the Republic of Croatia. Acta Hortic. 2018;(1199):391­6. doi:10.17660/actahortic.2018.1199.62.

40. Oliveira MC, Ramos JD, Pio R, Cardoso MG. Características fenológicas e físicas e perfil de ácidos graxos em oliveiras no sul de Minas Gerais. Pesq Agropec Bras. 2012;47(1):30-5.

41. Bustan A, Kerem Z, Yermiyahu U, Ben-Gal A, Lichter A, Droby S, Zchori-Fein E, Orbach D, Zipori I, Dag A. Preharvest circumstances leading to elevated oil acidity in ‘Barnea’ olives. Sci Hortic. 2014;176: 11-21. doi:10.1016/j.scienta.2014.06.028.45.

42. Martins FB, Ferreira MC, Silva LFO, Ramalho VRM, Gonçalves ED. Temperatura do ar no desenvolvimento reprodutivo de cultivares de oliveira. Rev Bras Meteorol. 2019;34(2):179-90. doi:10.1590/0102-77863340022.

43. Talhinhas P, Mota-Capitão C, Martins S, Ramos AP, Neves-Martins J, Guerra-Guimarães L, Várzea V, Silva MC, Sreenivasaprasad S, Oliveira H. Epidemiology, histopathology and aetiology of olive anthracnose caused by Colletotrichum acutatum and C. gloeosporioides in Portugal. Plant Pathol. 2011;60(3):483-95. doi:10.1111/j.1365-3059.2010.02397.x.

44. Rondanini DP, Castro DN, Searles PS, Rousseaux MC. Contrasting patterns of fatty acid composition and oil accumulation during fruit growth in several olive varieties and locations in a non-Mediterranean region. Eur J Agr. 2014;52(B):237-46. doi:10.1016/j.eja.2013.09.002.

45. Trentacoste ER, Puertas CM, Sadras VO. Modelling the intraspecific variation in the dynamics of fruit growth, oil and water concentration in olive (Olea europaea L.). Eur J Agr. 2012;38:83-93. doi:10.1016/j.eja.2012.01.001.

46. Ometto JC. Bioclimatologia vegetal. São Paulo: Editora Agronômica Ceres; 1981. 425p.

Supplementary material

Pluvial precipitation and mean air relative humidity from August 1 to November
15 in 3 crop seasons, Chapecó, Brazil. Data from the automatic weather station 1041 – Epagri (Chapecó, 27,09°S/52,64°W, 687 m of
elevation)(16)
Figure 1
Pluvial precipitation and mean air relative humidity from August 1 to November 15 in 3 crop seasons, Chapecó, Brazil. Data from the automatic weather station 1041 – Epagri (Chapecó, 27,09°S/52,64°W, 687 m of elevation)(16)

Daily occurrence of degree-days from May to July in 3 years, Chapecó, Brazil.
Data calculated using weather observation from the automatic weather station 1041 – Epagri (Chapecó, 27,09°S/52,64°W, 687 m of
elevation)(16), using a model from Ometto(46), minimum basal temperature = 9.1(25)
and maximum basal temperature = 40. Arrows indicate when the first
inflorescence was observed in stage 53
Figure 2
Daily occurrence of degree-days from May to July in 3 years, Chapecó, Brazil. Data calculated using weather observation from the automatic weather station 1041 – Epagri (Chapecó, 27,09°S/52,64°W, 687 m of elevation)(16), using a model from Ometto(46), minimum basal temperature = 9.1(25) and maximum basal temperature = 40. Arrows indicate when the first inflorescence was observed in stage 53

In
the upper chart, chilling units accumulated from May to July in 3 years,
Chapecó, Brazil. Arrows indicate when the first inflorescence was observed in
stage 53. In the bottom, accumulated number of days with minimum temperature
under 16 °C. Data calculated using weather observation from the automatic
weather station 1041 – Epagri (Chapecó,
27,09°S/52,64°W, 687 m of elevation)(16).
Chilling units calculated using the Model 1 of De Melo-Abreu(25) and modifying the starting date for May 1
Figure 3
In the upper chart, chilling units accumulated from May to July in 3 years, Chapecó, Brazil. Arrows indicate when the first inflorescence was observed in stage 53. In the bottom, accumulated number of days with minimum temperature under 16 °C. Data calculated using weather observation from the automatic weather station 1041 – Epagri (Chapecó, 27,09°S/52,64°W, 687 m of elevation)(16). Chilling units calculated using the Model 1 of De Melo-Abreu(25) and modifying the starting date for May 1

Asynchrony
in flower/fruit development. Chapecó, Brazil, September 2020
Figure 4
Asynchrony in flower/fruit development. Chapecó, Brazil, September 2020

Daily average air temperature (black line) and air temperature range (gray
area) observed in Chapecó, in 3 growth seasons. Data from the automatic weather
station 1041 – Epagri (Chapecó, 27,09°S/52,64°W, 687 m
of elevation)(16)
Figure 5
Daily average air temperature (black line) and air temperature range (gray area) observed in Chapecó, in 3 growth seasons. Data from the automatic weather station 1041 – Epagri (Chapecó, 27,09°S/52,64°W, 687 m of elevation)(16)

 

Additional information

Editor: Andrés Coniberti (https://orcid.org/0000-0002-5739-9628) Instituto Nacional de Investigación Agropecuaria (INIA), Montevideo, Uruguay

Author contribution statement: Eduardo Cesar Brugnara planned, designed, and executed the experiment, analyzed the data and wrote the manuscript. Rafael Roveri Sabião executed the experiment, analyzed the data, and helped on reviewing literature and the entire text of the manuscript.