Production of cuttings and nutrient export by Coffea canéfora in different periods in the Southwestern Amazon

Produção de estacas e exportação de nutrientes por Coffea canephora em diferentes épocas na Amazônia Sul Ocidental

ABSTRACT

Cutting is the main vegetative propagation method used for the production of Coffea canephora plantlets. In this method, parent plants are conducted in a specific field, called clonal garden, which must be managed to produce clonal cuttings. The objective of this study was to evaluate the production of cuttings and the export of nutrients by Coffea canephora in different periods in the Southwestern Amazon. The experiment was carried out in a 6 × 3 split-plot scheme (repeated measures in time), consisting of the combination of six clonal Coffea canephora genotypes (plot) and three cutting collection periods (subplots). The genotypes were: C-057, C-088, C-089, C-125, C-130 and C-160; and the evaluation sampling times were January/2017, May/2017 and September/2017. The applied design was a completely randomized design with four repetitions. The dry season, from May to September, promotes lower orthotropic stem dry mass accumulation by Coffea canephora, but allows obtaining a larger number of viable cuttings for the production of clonal plantlets. Nutrient accumulation by orthotropic stems for cutting production follows the following order: N > K > Ca > Mg > S > P > Mn > Fe > Zn > Cu. Nutrient export by the cuttings follows a descending order: K > N > Ca > Mg > P > S > Mn > Fe > Zn > Cu.

Key words: conilon coffee; clonal genotypes; vegetative propagules

RESUMO

A estaquia é o principal método de propagação vegetativa utilizado na produção de mudas de Coffea canephora. Neste método, são utilizadas matrizes conduzidas em um campo específico, denominado de jardim clonal, que deve ser manejado para produção de estacas clonais. Assim, objetivou-se avaliar a produção de estacas e a exportação de nutrientes por cafeeiros Coffea canephora em diferentes épocas na Amazônia Sul Ocidental. O experimento foi conduzido em esquema de parcelas subdivididas no tempo, 6 × 3, formado pela combinação de seis genótipos clonais de Coffea canephora (parcela) e três épocas de coleta de estacas (sub parcelas). Os genótipos foram: C-057, C-088, C-089, C-125, C-130 e C-160; e as épocas de coleta de avaliação foram: janeiro/2017, maio/2017 e setembro/2017. O delineamento foi o inteiramente casualizado com quatro repetições. O período de estiagem, que foi de maio a setembro, proporciona menor acúmulo de massa seca de hastes ortotrópicas por plantas matrizes de Coffea canephora, porém, possibilita a obtenção de maior número de estacas viáveis para produção de mudas clonais. O acúmulo de nutrientes pelas hastes ortotrópicas destinadas a produção de estacas segue a seguinte ordem: N > K > Ca > Mg > S > P > Mn > Fe > Zn > Cu. A exportação de nutrientes pelas estacas segue ordem decrescente: K > N > Ca > Mg > P > S > Mn > Fe > Zn > Cu.

Palavras-chave: café conilon; genótipos clonais; propágulos vegetativos

Introduction

The formation of high-yielding commercial orchards of Coffea canephora is directly linked to the use of good-quality plantlets (Ferrão et al., 2017). Cutting stands out as a method of vegetative propagation which ensures the maintenance of the genetic characteristics of the parent plant (Souza et al., 2015). In addition to genetic quality, plantlets must show sanitary and physiological quality.

The main factor that will determine the sanitary and physiological quality of the plantlets is the health of the parent plant. Although the technical recommendations indicate the exclusive use of parent plants for the production of cuttings, in the Amazon, cuttings have been collected in commercial orchards. As a consequence, the beginning of plantlet production is restricted to the months from July to September, corresponding to three, four or five months after the harvest and preparation of the parent plants. Thus, the period of planting the plantlets in the field is restricted to the months from October to December (Espindula et al., 2015) and from January to February.

Although the months from October to February are considered favorable for planting because they have high levels of precipitation, planting in this period results in a poor harvest in the first year after planting (Partelli et al., 2006), being economically unfeasible. As a way to solve this problem, the use of technologies such as irrigation has allowed the planting period to be altered and coffee orchards to be planted throughout the year.

However, C. canephora has seasonal variations in its growth along the year, a fact mainly influenced by the climatic conditions (Dubberstein et al., 2017), which may result in different nutritional composition of the vegetative aerial parts and, consequently, of the cuttings that will originate the plantlets. Thus, the objective of this study was to evaluate the productive capacity and nutritional composition of orthotropic stems of C. canephora coffee plants intended for the production of cuttings in different periods of the year in Southwestern Amazon.

Material and Methods

The experiment was conducted in the Experimental Area of EMBRAPA (10º 43’ 55” S; 62º 15’ 19” W, at an altitude of 300 m), in the municipality of Ouro Preto do Oeste, Rondônia, Brazil, from September 2016 to September 2017. The predominant climate in the region is rainy tropical - Aw (Alvares et al., 2013), with an average annual temperature of 25 °C and average precipitation of 2,000 mm year^-1. The rainy season occurs from October-November until April-May.

The experimental area consisted of an orchard of C. canephora, ‘Conilon - BRS Ouro Preto’ variety, planted for the exclusive purpose of producing cuttings in a soil classified as Ultisol. The orchard was planted in 2012, with spacing of 2.5 m between rows and 1.5 m between plants. Fertilization was performed following technical recommendations for the crop, intended for fruit production (Marcolan et al., 2015).

The experiment was conducted in a 6 × 3 split-plot scheme (repeated measures in time), consisting of six genotypes and three periods of cutting harvesting (January/2017, May/2017 and September/2017). The genotypes C-057, C-088, C-089, C-125, C-130 and C-160 of the variety Conilon - BRS Ouro Preto were used because they have similar phenotypic characteristics and because they represent the average behavior of this variety, which is composed of 15 genotypes (Ramalho et al., 2014). The experimental design was completely randomized with four repetitions.

The average values of minimum, mean and maximum temperature and air relative humidity and the precipitation along the experimental period were obtained by an automatic weather station installed in the above-mentioned experimental area (Figures 1A, B and C). To replace the evapotranspired water, complementary irrigation was performed using a conventional sprinkler system along the months of drought (Figure 1C).

Figure 1
Minimum, mean and maximum air temperature (A); minimum, mean and maximum air relative humidity (B); and accumulated precipitation and complementary irrigation (C) along the experimental period

The last fertilization of the parent plants, prior to experiment installation, was carried out in August 2016 (45 days before the experiment). This fertilization consisted of 150 g of 20-05-20, 50 g of MIB (B = 1.8%; Cu = 0.8%; Fe = 3.0%; Mn = 2.0%; Mo = 0.1%), 20 g of boric acid and 20 g of magnesium sulfate. In order to neutralize exchangeable aluminum and increase Ca and Mg contents, 200 g plant^-1 of dolomitic limestone (RNV 100%) was applied broadcast, 100 g on each side of the plant, covering approximately 1 m² of the soil.

Prior to installation of experiment (September/2016), the area was characterized by soil analysis in the 0-20 and 20-40 cm layers. In the first layer, the results were: pH = 5.6 in water; P = 46.5 mg dm^-3; K, Ca, Mg, H+Al, Al and CEC = 0.57, 2.13, 0.59, 4.8,0.22 and 8.18 cmol_c dm^-3, respectively, OM = 15.3 g kg^-1; Cu, Fe, Mn and Zn = 11, 95.19, 196.49 and27.6 mg dm^-3, respectively. In the 20-40 cm layer, the results were: pH = 6.3 in water; P = 34 mg dm^-3; K, Ca, Mg, H+Al, Al and CEC = 0.46, 3.68, 0.94, 1.7, 0 and 6.73 cmol_c dm^-3, respectively; OM = 5.8 g kg^-1; Cu, Fe, Mn and Zn = 7.16, 79.2, 158.03 and 14.76 mg dm^-3, respectively.

The parent plants intended for the production of cuttings were all standardized at the time of experiment installation (September/2016) with four orthotropic stems and induced to produce secondary shoots. To induce the shoots, two opposing stems received apical pruning, remaining with 1.70 m height from the soil level. All productive branches that were more than 30 cm long were removed. Foliar evaluation of the plants at the time of experiment installation indicated the following contents: N, P, K, Ca, Mg and S = 35, 1.09,26.9, 41.4, 3.31 and 2.29 g kg^-1, respectively, and Cu, Fe, Mn and Zn = 37.31, 310.5, 769.9 and 54.5 mg kg^-1 dry mass, respectively. During each growth cycle of the stems, 150 g of the 20-05-20 formulation were applied, split into two applications at 20 and 45 days after pruning.

The cuttings were produced from orthotropic stems collected in each one of the months indicated in the treatments. The apical and basal portions of the stems were eliminated using pruning shears. After that, all plagiotropic branches and 2/3 of the blade of each leaf were removed. Finally, the cuttings were individualized with two straight cuts: one immediately above the insertion point of the plagiotropic branches and the other at 5 cm below the insertion point of the pair of leaves (Aquino et al., 2017).

In each evaluation period, the following variables were measured: number of viable cuttings per parent plant, dry mass of viable cuttings, total dry mass of orthotropic stems, nutrient accumulation in orthotropic stems and the export of nutrients by the cuttings: nitrogen (N), phosphorus (P), potassium (K), calcium (Ca), magnesium (Mg), sulfur (S), copper (Cu), zinc (Zn), iron (Fe) and manganese (Mn).

To determine the nutrient accumulation in orthotropic stems, the vegetative material was collected in each evaluation period. After collection, the plant materials were placed in paper bags and taken to the oven, being exposed to a temperature of 65 °C until reaching constant mass. Subsequently, the samples were ground and subjected to the analysis of the nutrient contents. Nitric-perchloric chemical digestion was used for the nutrients P, K, Ca, Mg, Mn, Fe, Zn and Cu, followed by analytical determination by plasma spectrometry for Ca, Mg, Mn, Fe, Zn and Cu. P was determined by molecular spectrophotometry and K by flame photometry. N was obtained by sulfuric acid digestion and determined after distillation by the semi-micro Kjeldahl method (Carmo et al., 2000).

The accumulation of nutrients in the orthotropic stems of the coffee plant was calculated by multiplying the nutrient contents by the respective values of dry mass of the orthotropic stems (Acc = DMOS × C), in which Acc - nutrient accumulation, DMOS - dry mass of orthotropic stems, and C - nutrient content.

Nutrient export by the cuttings was determined by multiplying the nutrient concentration found in viable cuttings by the respective dry mass values of the cuttings (E = DMVC × C), in which E - nutrient export, DMVC - dry mass of viable cuttings, and C - nutrient content. The results were expressed in gram or milligram per plant.

The data were subjected to the Lilliefors’ test for normality assessment. The variables number of cuttings, dry mass of cuttings and orthotropic stems, K accumulation and S accumulation followed normal distribution. The other data were transformed to √x or log x, in order to obtain normal distribution. After transformation, analysis of variance and F test were carried out at p ≤ 0.05. The means were compared by Tukey and Scott-Knott tests (p ≤ 0.05), using the statistical program GENES^®.

Results and Discussion

There was interaction between the factors dry mass of the orthotropic stems and the accumulation of N, P, K, Ca, Mg, Cu and Mn in the orthotropic stems. For the cuttings, there was only interaction for the export of Zn and Cu.

The highest number and dry mass of cuttings were obtained in September, compared to the periods of January and May (Table 1). This suggests that parent plants of C. canephora that originated these cuttings invested more photoassimilates in the formation of nodes than in internode elongation, that is, they produced shorter internodes.

Table 1
Number of cuttings, dry mass of cuttings and dry mass of orthotropic stems of ‘Conilon’ Coffea canephora genotypes evaluated in different periods of the year

Genotype	Jan	May	Sep	Mean	Jan	May	Sep	Mean
	Number of cuttings				Dry mass of cuttings
	(cuttings plant-1)				(g plant-1)
C-057	128	146	222	165 a	135	189.6	270.4	198.3 a
C-088	149	157	194	166 a	163.2	214.7	232.5	203.5 a
C-089	110	124	174	136 a	120.6	130.1	168.1	139.6 a
C-125	120	124	175	139 a	156.6	178.9	228.6	188 a
C-130	116	130	174	140 a	140.9	175.4	197.9	171.4 a
C-160	117	119	187	141 a	145.3	136.1	210.1	163.8 a
Mean	123 B	133 B	187 A	148	143.6 B	170.8 AB	217.9 A	175.5
CV (%)1	31.29				33.32
CV (%)2	15.68				22.11
	January		May		September		Mean
	Dry mass of orthotropic stems
	(g plant-1)
C-S057	1,754 ABb		2,128 Aa		1,357 Ba		1,746 a
C-S088	2,118 Aa		1,971 Aa		1,135 Ba		1,741 a
C-S089	1,387 Ac		1,320 Abc		830 Bb		1,179 a
C-125	1,946 Aa		1,707 Ab		1,163 Ba		1,605 a
C-130	1,456 ABc		1,925 Aa		976 Bb		1,452 a
C-160	1,742 Ab		1,642 ABb		1,143 Ba		1,509 a
Mean	1,734 A		1,782 A		1,101 B		1,539
CV (%)1	30.13
CV (%)2	11.91

• Means followed by the same letters, uppercase in the row and lowercase in the column, do not differ by Tukey and Scott-Knott tests, respectively, both at p ≤ 0.05; ¹ Coefficient of variation of the subplot (period); ² Coefficient of variation of the plot (genotype)

Such reduction in the elongation of the orthotropic stem may be associated with the increase of temperatures and reduction in the air relative humidity observed during the growth period of the stems (Figure 1), since recent studies carried out with this species have shown that exposure to supra-optimal temperatures alone does not have any negative effect on photosynthesis and, consequently, on growth (Martins et al., 2016; Rodrigues et al., 2016). However, high temperatures associated with reduction in the air relative humidity lead to increased vapor pressure deficit. Such increment reduces plant growth due to stomatal limitations which interfere with the production of carbohydrates through photosynthesis (Thioune et al., 2017; Rodrigues et al., 2018).

In addition, the lowest dry mass accumulation in the orthotropic stems (Table 1) observed in September may be associated with the lower Zn accumulation found in the stems in this period. Zn participates in the synthesis of the amino acid tryptophan and is a precursor of indole acetic acid (AIA), a phytohormone related to cell growth and elongation and protein synthesis (Sadeghzadeh, 2013), whose lower availability in the plant is characterized by a reduction in the growth of internodes (Taiz et al., 2017). Thus, the lower internode elongation may have allowed an increase of nodes in the orthotropic stems, with consequent increase in the production of viable cuttings.

On the other hand, there was a lower production of viable cuttings and lower mass of cuttings, although there was higher production of dry mass of orthotropic stems in the periods of January and May (Table 1). This suggests that the stems showed elongation, which resulted in the growth of the internodes, to the detriment of the formation of nodes. This behavior may be associated with lower exposure of parent plants to solar radiation during the stem formation period (INPE, 2018), a condition that is determinant for promoting changes in growth pattern (Partelli et al., 2014), leading to etiolation of the branches.

Regarding macronutrient accumulation, in general, the orthotropic stems collected in September showed lower accumulation of nutrients, except sulfur, for which there was no difference in the accumulation between the production periods (Table 2). This lower nutrient accumulation observed in the orthotropic stems is possibly related to the flowering of the coffee plant, which occurred between August and September, because, during the reproductive stage, the flowers function as a strong sink of nutrients, especially N and K, absorbing 20 to 25% of the nutrients accumulated in the leaves (Laviola et al., 2006).

Table 2
Macronutrients accumulated in the vegetative dry mass (orthotropic stems) of ‘Conilon’ Coffea canephora genotypes in different periods of the year

Genotype	Jan	May	Sep	Mean	Jan	May	Sep	Mean
	N accumulation in stems				P accumulation in stems
	(g plant-1)
C-057	55 ABa	61.2 Aa	38.8 Ba	51.6 a	2.41 Ba	3.74 Aa	1.96 Ba	2.7 a
C-088	66.5 Aa	62.7 Aa	34.1 Ba	54.4 a	2.79 Aa	3.48 Aa	1.72 Ba	2.66 a
C-089	42.8 Ab	39.1 ABc	26 Bb	35.9 a	1.97 Ab	2.13 Ab	1.12 Ba	1.74 a
C-125	61.3 Aa	56.8 Aa	33.9 Ba	50.6 a	2.74 Aa	2.73 Ab	1.51 Ba	2.32 a
C-130	48.2 Ab	51.4 Ab	27.8 Bb	42.4 a	1.85 Bb	2.35 Ab	1.28 Bb	1.82 a
C-160	65.8 Aa	44.7 ABc	31.6 Bb	47.3 a	2.7 Aa	2.4 ABb	1.6 Ba	2.23 a
Mean	56.6 A	52.6 A	32 B	47.1	2.41 A	2.8 A	1.53 B	2.24
CV (%)1	17.86				17.85
CV (%)2	6.37				7.22
	K accumulation in stems				Ca accumulation in stems
	(g plant-1)
C-057	45.3 ABc	54.4 Aa	35.3 Ba	45 a	24.7 Ab	26.7 Aa	15.9 Ba	22.4 a
C-088	55.2 Ab	58.2 Aa	34.5 Ba	49.3 a	30.8 Aa	23.8 Aa	13.9 Ba	22.8 a
C-089	36.9 Ac	35.7 Ab	23.7 Ab	32.1 a	13.1 Ac	12 Ac	9.9 Ab	11.7 a
C-125	64.3 Aa	54.6 Aa	32.8 Ba	50.6 a	15.9 Ac	12.9 Ac	11.4 Ab	13.4 a
C-130	40.4 Ac	44.4 Ab	23.1 Bb	36 a	14.6 Ac	16.8 Ab	8.6 Bb	13.3 a
C-160	54.9 Ab	40.6 ABb	32.9 Ba	42.8 a	24.9 Ab	17.1 ABb	12.7 Bb	18.2 a
Mean	49.5 A	48 A	30.4 B	42.6	20.7 A	18.2 A	12.1 B	17
CV (%)1	30.45				14.25
CV (%)2	14.59				6.40
	Mg accumulation in stems				S accumulation in stems
	(g plant-1)
C-057	4 ABb	4.7 Aa	2.8 Ba	3.8 a	2.96	3.3	2.39	2.88 a
C-088	5.8 Aa	5.7 Aa	3 Ba	4.8 a	3.27	2.99	2.4	2.89 a
C-089	3.2 Ac	3 Ac	2.1 Ab	2.7 a	1.72	1.85	1.57	1.71 a
C-125	5.1 Aa	5.2 Aa	3.3 Ba	4.5 a	2.71	1.96	2.14	2.27 a
C-130	3 ABc	3.6 Ab	2.2 Bb	2.9 a	2.56	2.4	1.83	2.27 a
C-160	5.3 Aa	4.1 ABb	3.1 Ba	4.1 a	2.45	2.05	1.54	2.01 a
Mean	4.4 A	4.3 A	2.7 B	3.8	2.61 A	2.42 A	1.98 A	2.34
CV (%)1	17.06				40.65
CV (%)2	6.66				21.46

• Means followed by the same letters, uppercase in the row and lowercase in the column, do not differ by Tukey and Scott-Knott tests, respectively, both at p ≤ 0.05 level; N - Nitrogen; P - Phosphorus; K - Potassium; Ca - Calcium; Mg - Magnesium; S - Sulfur; ¹ Coefficient of variation of the subplot (period); ² Coefficient of variation of the plot (genotype)

In addition, in the case of S, this is an element considered of low mobility in the phloem (Taiz et al., 2017). In the plant, sulfate is the main form of S reserve, and it is not easily remobilized to young leaves (Lavres Junior et al., 2009), which justifies the similar S accumulation in all periods of production of orthotropic stems, as they constituted the main sink.

Regarding the effect of the genotypes, there was no uniformity of behavior for the accumulation of nutrients in the different periods evaluated, i.e., no genotype stood out positively or negatively, in general, from the others. There were only specific results that do not allow the genotypes to differentiated in relation to their behavior in terms of nutrient accumulation in the vegetative aerial part (Tables 2 and 3).

Table 3
Micronutrients accumulated in the vegetative dry mass (orthotropic stems) of ‘Conilon’ Coffea canephora genotypes in different periods of the year

Genotype	Jan	May	Sep	Mean	Jan	May	Sep	Mean
	Cu accumulation in stems				Fe accumulation in stems
	(mg plant-1)
C-057	47 Aa	49.9 Aa	58.2 Aa	47a	84	392	447	308 a
C-088	62.1 Aa	46.2 ABa	38.5 Bb	62.1 a	126	335	516	326 a
C-089	44.3 Aa	38.5 Aa	31.4 Ab	44.3 a	77	295	378	250 a
C-125	47.4 Aa	47.3 Aa	49 Aa	47.4 a	185	397	533	372 a
C-130	29.1 Bb	58.6 Aa	39 ABb	29.1 b	260	1.099	382	581 a
C-160	50.8 Aa	50.6 Aa	28.3 Bb	50.8 a	467	687	445	533 a
Mean	47 A	49.9 A	58.2 A	47 A	200 B	534 A	450 A	395
CV (%)1	19.41				7.40
CV (%)2	10.50				9.01
	Zn accumulation in stems				Mn accumulation in stems
	(mg plant-1)
C-057	94.2	116.9	27.4	79.5 a	378 Ab	373 Ab	256 Aa	335 a
C-088	134.4	36.5	24.6	65.2 a	674 Aa	373 ABb	278 Ba	441 a
C-089	79.5	64.9	26.4	56.9 a	670 Aa	425 ABb	260 Ba	451 a
C-125	107.9	97.5	27.5	77.6 a	945 Aa	718 ABa	390 Ba	684 a
C-130	112.8	42.3	28.2	61.1 a	845 Aa	775 Aa	213 Ba	611 a
C-160	57.4	43.5	74.1	58.3 a	947 Aa	384 Bb	297 Ba	543 a
Mean	97.7 A	66.9 AB	34.7 B	66.4	743 A	508 A	282 B	511
CV (%)1	13.05				10.34
CV (%)2	16.43				4.78

• Means followed by the same letters, uppercase in the row and lowercase in the column, do not differ by Tukey and Scott-Knott tests, respectively, both at p ≤ 0.05; Cu - Copper; Fe - Iron; Zn - Zinc; Mn - Manganese; ¹ Coefficient of variation of the subplot (period); ² Coefficient of variation of the plot (genotype)

The difference in the accumulation of macro- and micronutrients found in the orthotropic stems collected in different periods and for the various genotypes of C. canephora (Tables 2 and 3) suggest that there is discrimination in terms of nutrient use efficiency among the genotypes (Amaral et al., 2011). However, considering that, regardless of the genotypes, September was the month which led to the lowest accumulation for most nutrients, except for Cu and Fe. These results suggest that the environmental conditions to which the parent plants were exposed during the growth of the stems influenced more the accumulation of nutrients than the individual capacity of each genotype to absorb and translocate nutrients.

Indeed, nutrient accumulation by plants depends on several factors, such as genotype (Amaral et al., 2011), age, plant organs and tissues, availability of light (Araújo et al., 2015) and environmental conditions (Prezotti & Bragança et al., 2013). In the case of the effect of genotypes, the impossibility of identifying dissimilar genotypes, in general, is due to the fact that the genotypes of the variety Conilon - BRS Ouro Preto have been selected and grouped according to their phenotypic characteristics (Ramalho et al., 2014).

In relation to the export of macronutrients, the cuttings from orthotropic stems produced in September had higher values, regardless of the genotype, except for phosphorus, whose export did not differ between the months of May and September (Table 4). Such higher nutrient export in September is directly related to the higher number of viable cuttings and higher dry mass accumulation (Prezotti & Bragança, 2013) obtained in this period, that is, the higher the quantity of plant material removed from the clonal garden, the larger the export of macro- and micronutrients.

Table 4
Export of macronutrients by cuttings (clonal propagules) of ‘Conilon’ Coffea canephora genotypes in different periods of the year

Genotype	Jan	May	Sep	Mean	Jan	May	Sep	Mean
	N export by cuttings				P export by cuttings
	(mg plant-1)
C-057	2,713	4,419	5,296	4,143 a	161	292	371	275 a
C-088	3,137	4,613	4,259	4,003 a	184	306	257	249 a
C-089	2,102	2,913	3,318	2,777 a	120	179	188	162 a
C-125	2,484	3,623	4055	3,387 a	114	216	228	186 a
C-130	2,509	3,340	3,649	3,166 a	144	206	233	194 a
C-160	2,513	3,130	4,252	3,298 a	160	177	240	193 a
Mean	2,576 B	3,673 AB	4,138 A	3,462	147 B	229 A	253 A	210
CV (%)1	17.73				20.01
CV (%)2	9.99				11.19
	K export by cuttings				Ca export by cuttings
	(mg plant-1)
C-057	3,492	5,169	6,750	5,137 a	1,436	1,962	3,088	2,162 a
C-088	4,679	5,799	6,054	5,511 a	1,720	2,187	2,695	2,201 a
C-089	3,244	3,578	5,047	3,956 a	916	1,085	1,603	1,201 a
C-125	3,903	4,525	5,736	4,722 a	996	1,146	1,323	1,155 a
C-130	3,252	3,813	5,386	4,151 a	1,289	1,415	1,632	1,445 a
C-160	3,391	3,352	5,640	4,128 a	1,357	1,278	2,087	1,574 a
Mean	3,660 B	4,373 AB	5,769 A	4,601	1,286 B	1,512 AB	2,071 A	1,623
CV (%)1	4.54				20.01
CV (%)2	2.29				11.19
	Mg export by cuttings				S export by cuttings
	(mg plant-1)
C-057	288	395	680	454 a	172	194	392	253 a
C-088	255	388	427	357 a	199	211	237	216 a
C-089	158	240	335	244 a	102	133	205	147 a
C-125	162	259	288	236 a	192	182	236	203 a
C-130	179	270	293	247 a	178	198	273	216 a
C-160	217	226	381	275 a	140	131	200	157 a
Mean	210 B	296 AB	401 A	302	164 B	175 AB	257 A	199
CV (%)1	7.30				22.03
CV (%)2	4.14				12.54

• Means followed by the same letters, uppercase in the row and lowercase in the column, do not differ by Tukey and Scott-Knott tests, respectively, both at p ≤ 0.05; N - Nitrogen; P - Phosphorus; K - Potassium; Ca - Calcium; Mg - Magnesium; S - Sulfur; ¹ Coefficient of variation of the subplot (period); ² Coefficient of variation of the plot (genotype)

The export of macronutrients by the cuttings of the clonal garden followed the following order: K > N > Ca > Mg > P > S (Table 4). This sequence is different from that reported for the nutrient export by fruits, N > K > Ca > P > S > Mg (Covre et al., 2016). These sequences diverge with respect to the order of the first and second most exported nutrients, N and K, and in the position of Mg, which in fruits is the sixth most exported nutrient, whereas in the cutting it is the fourth most exported, ahead of P and S.

In the case of K, the nutrient most exported by the cutting, ahead of N, unlike what occurs in fruits, its higher concentration in the cutting can contribute to lower cutting dehydration in the nursery. This is because K is related to the maintenance of cell turgor (Taiz et al., 2017) and to stomatal regulation (Cunha et al., 2009). However , it should be considered that there was high availability of K in the soil, 0.57 cmol_c dm^-3 in the 0-20 cm layer, which may have promoted consumption above the physiological needs of the plant.

For Mg, the higher concentration of this nutrient in the cutting is related to its functions in the plant, especially in the composition of the chlorophyll molecule (Taiz et al., 2017), which is present in both the leaf and the herbaceous stem of the cutting. Thus, for the nutritional management of the clonal garden, its peculiarities should be considered and, therefore, it should not be managed in the same way as commercial orchards intended for fruit production.

For the export of micronutrients, the cuttings produced from orthotropic stems collected in September showed higher export of Fe and Zn, regardless of genotype (Table 5). Cu export was higher for the genotypes C-057 and C-125 by the cuttings produced in September. On the other hand, Mn was the only micronutrient exported in similar quantities by the cuttings in the different periods. The decreasing sequence of micronutrient export by the cuttings was Mn > Fe > Zn > Cu, respectively. These results reinforce the idea that not only the accumulation of nutrients in orthotropic stems, but the pattern of macro- and micronutrient export in the present study are more related to the period of collection than to the individual efficiency of each genotype to absorb nutrients because, among the evaluated genotypes, none of the materials stood out as more promising in the accumulation of macro- and micronutrients for the different periods evaluated.

Table 5
Export of micronutrients by cuttings (clonal propagules) of ‘Conilon’ Coffea canephora coffee genotypes in different periods of the year

Genotype	Jan	May	Sep	Mean	Jan	May	Sep	Mean
	Cu export by cuttings				Fe export by cuttings
	(mg plant-1)
C-057	2.5 Ca	5.5 Ba	17.8 Aa	8.6 a	18.9	45.7	46.7	37.1 a
C-088	2.9 Ca	5.1 Ba	10.3 Ab	6.1 a	11.9	19	38	23 a
C-089	2.1 Ba	3.3 Bb	13.8 Ab	6.4 a	16.2	12.3	37.8	22.1 a
C-125	3.2 Ca	6 Ba	15.1 Aa	8.1 a	5.5	14.5	49.9	23.3 a
C-130	2.9 Ca	6.4 Ba	11.5 Ab	6.9 a	5	23.5	31.9	20.2 a
C-160	3.7 Ba	3.9 Bb	11.4 Ab	6.3 a	9.4	15.4	40.1	21.6 a
Mean	2.9 C	5 B	13.3 A	7.1	11.1 B	21.7 B	40.7 A	24.5
CV (%)1	22.37				35.60
CV (%)2	14.18				22.64
	Zn export by cuttings				Mn export by cuttings
	(mg plant-1)
C-057	8.9 Ba	2.4 Ca	85.1 Aa	32.1 a	33	28.5	42.2	34.6 b
C-088	12.2 Ba	3.7 Ca	53.2 Aa	23 a	33.6	32.3	33.5	33.1 b
C-089	7.2 Ba	2.7 Ca	30 Aa	13.3 a	51.1	39.2	51.4	47.3 a
C-125	9.8 Ba	6 Ca	35.3 Aa	17 a	55.4	65.7	63	61.4 a
C-130	7.6 Ba	6.4 Ca	18.2 Aa	10.7 a	81.5	50.7	57.4	63.2 a
C-160	8.4 Ba	1.9 Ca	19.9 Aa	10.1 a	58.5	40.2	55.2	51.3a
Mean	9 B	3.8 C	40.3 A	17.7	52.2 A	42.8 A	50.5 A	48.4
CV (%)1	26.18				30.57
CV (%)2	19.37				13.97

• Means followed by the same letters, uppercase in the row and lowercase in the column, do not differ by Tukey and Scott-Knott tests, respectively, both at p ≤ 0.05; Cu - Copper; Fe - Iron; Zn - Zinc; Mn - Manganese; ¹ Coefficient of variation of the subplot (period); ² Coefficient of variation of the plot (genotypes)

Information on the amount of nutrients exported from the clonal garden through the removal of cuttings for the production of plantlets guides its fertilizer replacement, given that fertilizer replacement in clonal gardens is currently based on the production fertilization of commercial orchards. However, other factors should be considered when it comes to fertilizer replacement in clonal gardens, because the nutrients that return to the system through the dry mass of the remaining orthotropic stems of the cuttings undergo losses through several processes, such as immobilization (Lima et al., 2005), mineralization, volatilization (Diniz et al., 2014) and erosion (Sousa et al., 2012). Therefore, all nutrient losses should be taken into consideration for the fertilizer replacement.

Conclusions

1. The dry season, from May to September, leads to lower orthotropic stem dry mass accumulation by C. canephora parent plants, but allows obtaining a greater number of viable cuttings.

2. Nutrient accumulation by orthotropic stems intended for the production of cuttings follows the following descending order: N > K > Ca > Mg > S > P > Mn > Fe > Zn > Cu. The values are 47.1, 42.6, 17, 3.8, 2.34 and 2.24 g per plant per cut for N, K, Ca, Mg, S and P, respectively, and 511, 395, 66.4 and 47 mg per plant per cut for Mn, Fe, Zn and Cu.

3. The cuttings used for the production of clonal plantlets of C. canephora are responsible for average exports of 4,138, 3,462, 1,623, 302, 210, 199, 48.4, 24.5, 17.7 and 7.1 mg per plant per cut of K, N, Ca, Mg, P, S, Mn, Fe, Zn and Cu, respectively, from the clonal garden.

Acknowledgments

To Consórcio Pesquisa Café, for the financial support, and to CNPq and CAPES for granting scholarships.

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Publication Dates

• Publication in this collection
  02 Mar 2020
• Date of issue
  Mar 2020

History

• Received
  16 Sept 2018
• Accepted
  31 Dec 2019
• Published
  12 Feb 2020