ABSTRACT:
Proper plant nutrition is critical to increasing the yield of bananas. The objective was to establish the potential nutrient-response curves and sufficiency ranges using the boundary line approach (BLA) and the method proposed by Kenworthy (MK) to assess the nutritional status of ‘Prata-Anã’ bananas cultivated under two environmental conditions. The study was carried out using a database comprising leaf nutrient concentrations and banana yields grown at Missão Velha, Ceará, and Ponto Novo, Bahia, Brazil. The reference population consisted of high-yielding plants with yields greater than the mean yield plus 0.5 standard deviation. The database was divided into two datasets. One contained 253 leaf analysis results and a reference population with a mean yield greater than 39.81 t ha−1 yr−1 at Missão Velha. The other contained 147 samples and a reference population with a mean yield greater than 41.69 t ha−1 yr−1 at Ponto Novo. The sufficiency ranges obtained by the BLA for ‘Prata-Anã’ banana in Bahia and Ceará, respectively, are: a) for macronutrients (g kg−1): N (19.3-22.0) and (19.9-22.1); P (1.4-2.0) and (1.4-1.6); K (22.6-32.2) and (24.0-31.3); Ca (4.6-6.5) and (5.3-5.8); Mg (1.8-2.6) and (2.1-2.7); S (1.3-2.0) and (1.3-1.5); b) for micronutrients (mg kg−1): B (8.4-13.0) and (13.7-16.4); Cu (5.6-8.4) and (4.4-5.2); Fe (54.2-77.6) and (39.0-55.0); Mn (140.1-222.8) and (64.0-91.0); Zn (13.5-18.3) and (12.4-14.5). The sufficiency ranges obtained by the BLA are more assertive when assessing the nutritional status for ‘Prata-Anã’ banana.
Keywords: Musa spp; AAB; site condition; nutritional status; diagnostic methods
Introduction
Leaf tissue analysis as a tool for assessing plant nutritional status has been widely used to improve fertilizer rate recommendations and crop management practices. Reference values are conventionally established in calibration tests in which genetic and environmental factors and the interplay between nutrients are controlled; however, the nutritional composition of plant tissues is highly influenced by several environment- and crop-related factors (Iheshiulo et al., 2019). Indiscriminate extrapolations of sufficiency ranges established in diverse environmental conditions may lead to inaccurate nutritional diagnoses; thus, determining site- and cultivar-specific sufficiency ranges is a preferable course of action.
The boundary line approach (BLA) is an alternative to calibration experiments because this method uses nutrient concentration data from commercial crop fields (Maia and Morais, 2016). The approach consists of relating nutrient concentrations to yield data, so that the optimum concentration of a given nutrient can be determined. Moreover, it permits the estimation of the highest attainable yield from observational data (Ali, 2018).
Studies found in the literature report sufficiency ranges established by BLA for several crops including forage cactus (Blanco-Macías et al., 2010), papaya (Maia and Morais, 2016), sugarcane (Mccray et al., 2010), rubber tree (Njukeng et al., 2013), haskap (Iheshiulo et al., 2019) and eucalyptus (Lima Neto et al., 2020); however, studies on bananas are in short supply.
Bananas demand large amounts of nutrients and are sensitive to nutritional imbalances. Thus, periodically, nutritional diagnoses should be adopted as a routine procedure on banana plantations (Silva, 2015) based on specific norms established using data from commercial fields (Lafond, 2013).
The objective of this study was to establish potential nutrient-response curves for determining sufficiency ranges using the BLA and the method proposed by Kenworthy to assess the nutritional status of ‘Prata-Anã’ bananas cultivated under two environmental conditions.
Materials and Methods
Experimental conditions
he study was carried out using data from ‘Prata-Anã’ banana production systems under two environmental conditions. The first farm is located at Missão Velha, in the state of Ceará (CE), Brazil (7°35’90” S, 39°21’17” W, altitude of 442 m). Data were collected from plants averaging 12 years of age at the beginning of data collection and 19 by the end of it. The climate of the region is Aw – tropical savanna climate with a dry winter season and a rainy summer season (Köppen-Geiger) (Alvares et al., 2013). Mean annual rainfall and temperature are 942 mm and 25.8 °C, respectively. The soil was sandy and classified predominantly as a Red-Yellow Latosol (SiBCS) (Santos et al., 2018). On this farm, there are 57 plots averaging 3.26 ha in size of fertigated ‘Prata-Anã’ banana spaced at 2.8 × 2.8 m (1,275 plants ha−1).
The second farm is located at Ponto Novo, in the state of Bahia (BA), Brazil, (10°51’46” S, 40°08’01” W, and altitude of 342 m). Data collection began when bananas were eight years old and ended when they were ten. The climate is also Aw (Köppen-Geiger) (Alvares et al., 2013) with a mean annual rainfall of 697 mm and temperature 24.1 °C. The predominant soil at the site is a sandy Yellow Latosol (SiBCS) (Santos et al., 2018). On this farm, there are 100 plots averaging 4.53 ha in size of fertigated ‘Prata-Anã’ banana spaced at 2.8 × 2.8 m (1,275 plants ha−1).
Fertilizer rates recommended for both sites were based on their respective soil test results and followed Silva (2015) with adaptations. Table 1 and 2 show soil test results and climate data for both sites, respectively. Climate data are the year 2016, when weather stations were installed at the sites.
Soil chemical test results of ‘Prata-Anã’ banana fields at Missão Velha, CE, and Ponto Novo, BA, Brazil, 0.0-0.2 m and 0.2-0.4 m, for the period 2014-2016.
Database
The results of the analysis of the leaf tissue and the yields recorded in a database belonging to the experimental area were used. Leaf tissue sampling was performed twice a year, every six months, and followed the recommendations of Costa et al. (2019). The mid-portion of the third leaf lamina, counting from the apex, was collected when the inflorescence had two or three open clusters of male flowers. Samples were processed and analyzed as to leaf macro- (N, P, K, Ca, Mg and S) and micronutrient (B, Cu, Fe, Mn and Zn) contents, which were determined as follows: N – Kjeldahl method; P, S, Ca, Mg, Fe, Mn, Cu, Zn, B, Al – nitric-perchloric acid digestion and determination by ICP-OES; K – nitric-perchloric digestion and determination by flame photometer as described by Deus et al. (2018a).
Yields were estimated as t ha−1 yr−1 by weighing hands of harvested bunches. Relative yield (RY) was determined based on the highest recorded yield (100 %) as recorded by Deus et al. (2018b).
The database was divided into two site-specific datasets. A dataset was from the farm located at Missão Velha, CE, and comprised annual yields and leaf analysis results relative to the years from 2010 to 2017. The initial sample containing 804 recordings, mean ± standard deviation of 35.91 ± 7.8 t ha−1 yr−1, was subdivided into low- and high-yielding populations; the latter was the reference population, defined as having yields above the average plus 0.5 standard deviation, as used by Alves et al. (2019), which corresponded to 39.81 t ha−1 yr−1 (73 % maximum relative yield) (n = 253).
The other dataset was from the farm located at Ponto Novo, BA, and contained leaf analysis results from samples collected twice a year and annual yields recorded between 2014 and 2016. The initial sample consisting of 481 recordings, mean ± standard deviation of 34.89 ± 13.59 t ha−1 yr−1, was subdivided into low- and high-yielding populations. The reference population had a yield greater than average plus 0.5 standard deviation, corresponding to 41.69 t ha−1 yr−1 (57 % maximum relative yield) (n = 147).
Determination of potential nutrient-response curves, reference values and sufficiency ranges by the Boundary Line Approach (BLA)
Relative yields (RY), on the y-axis, were plotted against leaf nutrient concentrations, on the x-axis, forming a scatter diagram. Data points located on the upper edge of the scatter diagram were selected by drawing a line confining all data, forming a boundary line. Each data point on the upper boundary line represents the highest yield at a corresponding nutrient concentration. A regression equation fitted to the boundary line was used to determine sufficiency ranges.
A boundary line can be determined through different approaches (Deus et al., 2018a). The line around the scatter of data points can be drawn either by hand (Maia and Morais, 2016) or by using computer applications, such as Boundary Fit, developed by the Federal University of Viçosa (UFV) (Lima Neto et al., 2020). In this study, a nonparametric boundary regression (NPBR) package in R (R Development Core Team, 2012) was used as a routine for determining the boundary line.
Sufficiency ranges were obtained using the BLA based on the following interpretative categories: deficient (RY < 70 %), tending to sufficient (70 ≤ RY < 90 %), sufficient (90 ≤ RY < 100 %), high (100 > RY ≥ 90 %, to the right of the maximum), tending to excessive (90 ≤ RY < 70 %, to the right of the maximum) and excessive (RY < 70 %, to the right of the maximum).
Original Method proposed by Kenworthy (MKorig)
The mean and variability of leaf nutrient concentrations were obtained from the reference population of each site (Table 3). Percent of standard (P) (ratio of sample nutrient concentration to standard concentration), influence of variation (I) and coefficient of variation (CV) were calculated. The results were expressed in the form of a percentage. The following equations were used to calculate Kenworthy’s balance indices (BIKW):
Specific norms for calculating balances indices of Kenworthy for ‘Prata-Anã’ banana grown at Missão Velha, Ceará, and Ponto Novo, Bahia, Brazil.
where: P is the ratio of sample nutrient concentration (yi) to standard concentration (Ŷ) (%); I is the influence of variability (%); CV is the coefficient of variation (%) of nutrient concentrations in the reference population; and BIKW is the balance index proposed by Kenworthy.
The upper limit sufficient concentration ranges obtained by MKorig is the leaf nutrient concentration that corresponds to the BIKW of 100 %.
Sufficiency ranges were obtained based on interpretive classes originally proposed by Kenworthy (1961): deficient (BIKW < 50 %); tending to sufficient (50 ≤ BIKW < 83 %); sufficient (83 ≤ BIKW < 100 %); high (100 ≤ BIKW < 117 %); tending to excessive (117 ≤ BIKW < 150 %); and excessive (BIKW ≥ 150 %).
Modified Method proposed by Kenworthy (MKmod)
The ranges originally proposed by Kenworthy (1961) for apple trees may not be adequate because the author consistently used a mean variability of 20 % for every nutrient. This poses a problem when dealing with micronutrients because their leaf contents tend to have a variability higher than 20 %. Thus, the BLA was used to obtain nutrient-specific interpretive classes based on RY (Lima Neto et al., 2020)
After obtaining the BIKW for each nutrient studied using site-specific norms, RY was plotted against the BIKM to form a scatter of data points. Data points located on the upper boundary of the scatter diagram were selected, and were used to determine regression equations, with which the nutrient-specific interpretive classes were determined based on the following: deficient (RY < 70 %), tending to sufficient (70 ≤ RY < 90 %), sufficient (90 ≤ RY < 100 %), high (100 > RY ≥ 90 %, to the right of the maximum), tending to excessive (90 ≤ RY < 70 %, to the right of the maximum) and excessive (RY < 70 %, to the right of the maximum).
Results and Discussion
The original methodology proposed by Kenworthy (1961), MKorig, is based on the assumption that each nutrient limits crop yield equally; however, when using the BLA, the relationship between the RY and the BIKW (Figures 1A-K and 2A-K) yielded different interpretative classes (Table 4) for each nutrient, which contradicts Kenworthy’s approach. Differences across sufficiency ranges are mainly due to how yield-limiting the nutrient is when its concentration in plant tissues is at its lowest.
Boundary line fitted as a function of the relationship between relative yield (%) and indices of Kenworthy for N (A), P (B), K (C), Ca (D), Mg (E), S (F), B (G), Cu (H), Fe (I), Mn (J) and Zn (K) in ‘Prata-Anã’ banana, Missão Velha, CE, Brazil. **Significant at p ≤ 0.01 by the t-test; The multipliers 1.018; 1.0122; etc. found in the equations correspond to an adjustment factor for the equation to assume the value of 100 % Relative Yield.
Boundary line fitted as a function of the relationship between relative yield (%) and indices of Kenworthy for N (A), P (B), K (C), Ca (D), Mg (E), S (F), B (G),Cu (H), Fe (I), Mn (J) and Zn (K) in ‘Prata-Anã’ banana, Ponto Novo, BA, Brazil. **Significant at p ≤ 0.01 by the t-test; The multipliers 1.1235; 1.0741; etc. found in the equations correspond to an adjustment factor for the equation to assume the value of 100 % Relative Yield.
Proposed interpretive classes for discriminating balance indices of Kenworthy (%) for ‘Prata-Anã’ banana grown at Missão Velha, CE, and Ponto Novo, BA, Brazil.
Apparently, the interpretive classes originally proposed by Kenworthy were based on a mean variability of 20 % for macro- and micronutrients alike. As micronutrient concentrations vary greatly in banana leaves, misleading interpretations are more likely to arise owing to their complex dynamics within the soil-plant system (Li et al., 2007; Rengel, 2015).
For each nutrient, regression equations were fitted to a boundary line fitted to the relationship between the RY and the BIKW of ‘Prata-Anã’ banana grown in CE and BA (Figures 1A-K and 2A-K) with high R2 (0.92 to 0.97). The regression equations were used to obtain nutrient-specific interpretive classes used for discriminating the BIKW (Table 4).
Lower limits of ‘sufficient’ interpretive classes of ‘Prata-Anã’ banana grown in CE and BA (Table 4) were close to that proposed by Kenworthy (1961), (83 %), with greater differences for K (72 %), Cu (91 %), and B (75 %) in CE, and for N (75 %) and Cu (%) in BA. Upper limits were also close to those proposed for MKorig (100 %), except for P (115 %), S (121 %), Cu (126 %) and Mn (120 %) in CE, and for K (112 %) and Mn (119 %) in BA.
The BLA allowed for the fitting of significant quadratic regression equations with high R2 (0.91 to 0.98) to the upper boundary of the relationship between the RY and leaf nutrient concentrations in ‘Prata-Anã’ grown in CE (Figure 3A-K) and BA (Figure 4A-K). Sufficiency ranges were then estimated by regression equations (Table 5).
Boundary line fitted as a function of the relationship between relative yield (%) and leaf concentrations of N (A), P (B), K (C), Ca (D), Mg (E), S (F), B (G), Cu (H), Fe (I), Mn (J) and Zn (K) in ‘Prata-Anã’ banana, Missão Velha, CE, Brazil. **Significant at p ≤ 0.01 by the t-test; The multipliers 1.0318; 1.0332; etc. found in the equations correspond to an adjustment factor for the equation to assume the value of 100 % Relative Yield.
Boundary line fitted as a function of the relationship between relative yield (%) and leaf concentrations of N (A), P (B), K (C), Ca (D), Mg (E), S (F), B (G), Cu (H), Fe (I), Mn (J) and Zn (K) in ‘Prata-Anã’ banana, Ponto Novo, BA, Brazil. **Significant at p ≤ 0.01 by the t-test; The multipliers 1.1739; 1.1686; etc. found in the equations correspond to an adjustment factor for the equation to assume the value of 100 % Relative Yield.
Sufficiency ranges determined by boundary line approach for interpreting leaf nutrient concentrations in ‘Prata-Anã’ bananas grown at Missão Velha, CE, and Ponto Novo, BA, Brazil.
Sufficiency ranges obtained by MKmod for ‘Prata-Anã’ grown in CE and BA are in Table 6 while sufficiency ranges obtained by MKorig for CE and BA are in Table 7.
Proposed sufficiency ranges determined using modified method of Kenworthy for leaf nutrient concentrations in ‘Prata-Anã’ bananas cultivated at Missão Velha, CE, and Ponto Novo, BA, Brazil.
Leaf nutrient concentration ranges proposed by the original method of Kenworthy (1961) for ‘Prata-Anã’ bananas cultivated at Missão Velha, CE, and Ponto Novo, BA, Brazil.
The sufficient N concentration range established by the BLA for ‘Prata-Anã’ grown in CE was 19.2-22.0 g kg−1 (Table 5); very similar to that obtained by MKmod, 19.3-21.9 g kg−1, (Table 6) and close to MKorig, 17.9-21.9 g kg−1 (Table 7). For BA, the sufficient N concentration range obtained by the BLA was 19.9-22.1 g kg−1 (Table 5), with only the upper limit similar to that determined by MKmod, 16.4-22.2 g kg−1 (Table 6). The range was somewhat different from that proposed by MKorig, 18.5-23.0 g kg−1 (Table 7). |The sufficient N concentration ranges for Missão Velha, CE, are similar to that reported by Deus et al. (2018b) (18.0-26.8 g kg−1) for the same site and different from that reported by Silva (2015) for the same cultivar grown in northern Minas Gerais, Brazil (25.0-29.0 g kg−1). This difference was due to differences in soil organic matter levels and crop management.
Bananas grown on soils with medium-to-high organic matter content (> 16 g kg−1), such as those in this study (Table 1),are not likely to respond to N fertilization, and yields may even decrease as a result of excessive N applications (Silva, 2015). In addition, nutrient cycling plays a major role in replenishing the soil with N; up to 83 % of N returns to the soil after the harvest (Hoffmann et al., 2010). The increased N level in the soil resulted in a narrower sufficient N range than that reported by Silva (2015) and similar to that found by Deus et al. (2018b) in conditions akin to those of this study. This reduction in leaf N concentration was also observed by Damatto Junior et al. (2011), who reported a decrease in leaf N concentrations in ‘Prata-Anã’ banana subject to an increase in N supply.
The lower sufficient N concentration ranges reported in this study, in comparison with those reported by Silva (2015), agree with previously proposed reductions in N fertilizer rates (Deus et al., 2018a). In 1999, the recommended N fertilizer rate for ‘Prata-Anã’ grown in northern Minas Gerais ranged from 200 to 400 kg ha−1 yr−1, a rate range much greater than previous N recommendations, which ranged from 90 to 220 kg ha−1 yr−1 (Silva, 2015).
The sufficient P concentration range obtained by the BLA for ‘Prata-Anã’ grown in CE was 1.4-2.0 g kg−1 (Table 5); equal to the range found by MKmod (Table 6) and close to MKorig, 1.3-1.7 g kg−1 (Table 7). For BA, the sufficient range obtained by the BLA was 1.4-1.6 g kg−1 (Table 5), the same range determined by MKmod (Table 6) and very close to the range obtained by MKorig, 1.3-1.6 g kg−1 (Table 7). Similarly, Deus et al. (2018b) and Silva (2015) found the ranges 1.5-1.7 g kg−1 and 1.5-1.9 g kg−1, respectively; their lower variability is consistent with how banana plants respond to P (Silva, 2015).
Phosphorus is the macronutrient that accumulates the least in leaves of ‘Prata-Anã’ banana (Hoffmann et al., 2010). Increased leaf P concentrations may limit the yield due to imbalances in other nutrients, particularly Zn. Although soil P availability increases, leaf P concentration remains virtually unchanged (Damatto Junior et al., 2011). It has been reported that ‘Prata-Anã’ bananas only respond to P fertilization in the first cycle, even when grown on soils with low P levels (Silva, 2015).
The sufficient K concentration range obtained by the BLA for CE was 22.6-32.2 g kg−1 (Table 5). The range limits are closer to that found by MKmod, 22.3-32.3 g kg−1 (Table 6) than by MKorig, 26.9-34.0 g kg−1 (Table 7). For BA, the sufficient K concentration range obtained by the BLA was 24.0-31.3 g kg−1 (Table 5); different from the range determined by MKmod, 27.3-36.2 g kg−1 (Table 6) and similar to MKorig, 24.5-31.4 g kg−1 (Table 7). The range established by Silva (2015), 27.0-35.0 g kg−1, was closer to that obtained by MKorig while Deus et al. (2018b) reported a narrower, higher range, 32.0-37.4 g kg−1, which reflects how K moves within the soil-banana system, with greater variations in tissue concentration as a result of biochemical and geochemical cycling (Silva et al., 2015).
Although bananas demand large amounts of K, up to 86 % of the K taken up by banana plants is reutilized (Hoffmann et al., 2010) when plant residues left on the soil surface after the crop harvest break down. Nevertheless, K deficiency may reduce the relative growth of ‘Prata-Anã’ banana by 44 % (Silva et al., 2014).
The sufficient Ca concentration range obtained by the BLA for ‘Prata-Anã’ grown in CE was 4.6-6.5 g kg−1; similar to the ranges determined by MKmod and MKorig, 5.1-7.0 g kg−1 (Table 6) and 5.1-6.5 g kg−1 (Table 7), respectively. For BA, the sufficient range determined by the BLA was 5.3-5.8 g kg−1 (Table 5), whose lower and upper limits were different, but within the ranges obtained by MKmod (4.8-5.7 g kg−1) and MKorig (4.6-5.6 g kg−1) (Table 6 and 7, respectively). Ranges determined for both sites were close to that reported by Silva (2015), 4.5-7.5 g kg−1. Compared with ranges observed in this study, the sufficient Ca range reported by Deus et al. (2018b) was broader, 5.7-10.1 g kg−1, which might be associated with greater soil Ca levels in CE, the same soil used by the authors.
The sufficient Mg concentration established by the BLA for CE was 1.8-2.6 g kg−1 (Table 5); very close to MKmod and MKorig, 1.9-2.6 g kg−1 (Table 6) and 1.9-2.4 g kg−1 (Table 7), respectively. For BA, the sufficient Mg concentration range obtained by the BLA was 2.1-2.7 g kg−1 (Table 5), which is similar to that determined by MKmod and MKorig, 2.0-2.6 g kg−1 (Table 6) and 2.3-2.7 g kg−1 (Table 7), respectively. The sufficient Mg range determined by Silva (2015) was 2.4-4.0 g kg−1, whose lower limit is close to the upper limit of the sufficient Mg concentration ranges found in this study. Narrower ranges for Mg might be associated with the high K supply via fertigation to a soil containing high K levels (8.4 mmolc dm−3). Thus, the K/Mg ratio increased, which limited Mg uptake (Silva, 2015; Deus et al., 2018b).
Banana is a monocot and thus has low root cation exchange capacity, which means the plant can take up more monovalent cations to the detriment of divalent cations. Similarly,,high soil Ca levels, particularly in CE, contribute to decreases in Mg uptake by competitive inhibition. In a pot experiment withholding Mg, ‘Prata-Anã’ reduced growth by 67 % (Silva et al., 2014); therefore, one should be careful when supplying Mg to banana plants grown on soils containing high K levels, especially when the plants are under stress because Mg and K play an important role in alleviating plant stress (Marschner, 2012).
The sufficient S concentration range determined the BLA for ‘Prata-Anã’ grown in CE was 1.3-2.0 g kg−1 (Table 5), whose limits are close to those established by MKmod and MKorig, 1.2-1.6 g kg−1 (Table 6) and 1.3-1.9 g kg−1 (Table 7), respectively. For BA, the sufficient S concentrations by the BLA was 1.3-1.5 g kg−1 (Table 5), whose limits are close to those determined by MKmod and MKorig, 1.2-1.4 g kg−1 (Table 6) and 1.2-1.5 g kg−1 (Table 7), respectively. Silva (2015) established a sufficient S range of 1.7-2.0 g kg−1, similar to the ranges proposed herein, but narrower. The sulfur concentration range reported by Deus et al. (2018b) was even narrower, 1.4-1.6 g kg−1.
The sufficient B concentration range established by the BLA for ‘Prata-Anã’ cultivated in CE was 8.4-13.0 mg kg−1 (Table 5), while by MKmod and MKorig, the ranges were 6.4-11.6 mg kg−1 (Table 6) and 7.9-11.1 mg kg−1 (Table 7), respectively. For BA, the sufficient B concentration range obtained by the BLA was 13.7 to 16.4 mg kg−1 (Table 5). The range differs from those determined by MKmod and MKorig, 11.5-15.5 mg kg−1 (Table 6) and 11.7-14.7 mg kg−1, respectively. The sufficient B concentration range established for CE is lower than those proposed by Silva (2015), 12.0-25.0 mg kg−1, whose lower limit has the same value as the corresponding upper limit reported herein. The sufficient range established for BA was different, but within the range proposed by Silva (2015).
The sufficient Cu concentrations obtained by the BLA for ‘Prata-Anã’ grown in CE ranged from 5.6 to 8.4 mg kg−1 (Table 5), which is similar to the range determined by MKmod, 5.3-8.8 mg kg−1 (Table 6), but different from that obtained by MKorig, 4.5-6.2 mg kg−1 (Table 7). The sufficient Cu concentration range determined by the BLA for BA was 4.4-6.2 mg kg−1 (Table 5), whose limits are different from those determined by MKmod, 2.9-4.7 mg kg−1 (Table 6), and equal to the MKorig, 4.2-5.3 mg kg−1 (Table 7). Silva (2015) reported a sufficiency range of 2.6-8.8 mg kg−1, whose lower limit is different from those determined in CE by the BLA and MKmod, and altogether different from limits obtained by MKorig. For BA, all sufficient Cu ranges except the one obtained by MKmod were different from the range proposed by Silva (2015).
For CE, the sufficient Fe concentration range established by the BLA was 54.2-77.6 mg kg−1 (Table 5), by MKmod, 55.8-74.9 mg kg−1 (Table 6), and by MKorig, 53.3-67.4 mg kg−1 (Table 7). The sufficient Fe concentration range obtained by the BLA for ‘Prata-Anã’ grown in BA was 39.0 to 55.0 mg kg−1 (Table 5), whose lower limits differ from those established by MKmod, 42.5-58.9 mg kg−1 (Table 6) and by MKorig, 44.1-57.3 mg kg−1 (Table 7). All sufficient Fe concentration ranges reported herein were lower than that reported by Silva (2015), 72.0-157.0 mg kg−1.
The sufficient Mn concentration range established by the BLA for CE was 140.1-223.8 mg kg−1 (Table 5), different from ranges determined by MKmod, 120.1-253.5 mg kg−1 (Table 6) and by MKorig, 116.4-179.4 mg kg−1 (Table 7). The sufficient Mn concentration range obtained by the BLA was 64.0-91.0 mg kg−1 (Table 5), whose upper limit is different from that obtained by MKmod, 66.9-110.6 mg kg−1 (Table 6), and similar to that obtained by MKorig, 61.5-84.7 mg kg−1 (Table 7). These ranges were lower and narrower than that reported by Silva (2015), 173.0-630.0 mg kg−1.
Manganese is the most variable element in both CE (CV = 51.8 %) and BA (CV = 38.0 %). If leaf nutrient concentrations in a population have a CV higher than 30 %, the sufficiency ranges obtained by MKorig are less precise in detecting nutrient deficiencies. Moreover, Silva (2015) found a wider sufficient Mn range because the author did not use a correction factor (k) that is needed to narrow the range down (Alves et al., 2019) in the event of highly fluctuating tissue nutrient levels, mostly micronutrients with a CV higher than 20 %.
The sufficient Zn concentration range obtained by the BLA for CE was 13.5-18.3 mg kg−1 (Table 5), similar to the range determined by MKmod and MKorig, 12.9-18.3 mg kg−1 (Table 6) and 13.1-16.5 mg kg−1 (Table 7), respectively. For ‘Prata-Anã’ grown in BA, the sufficient Zn concentration range obtained by the BLA was 12.4-14.5 mg kg−1 (Table 5), similar to ranges obtained by MKmod and MKorig, 12.2-14.7 mg kg−1 (Table 6) and 12.0-14.8 mg kg−1 (Table 7), respectively. Proposed ranges for CE are close to that established by Silva (2015), 14.0-25.0 mg kg−1, despite the latter’s higher upper limit. As for BA, the upper limits were identical to the lower limits proposed by Silva (2015).
The sufficient ranges for micronutrients are less consistent with the literature than for macronutrients. Micronutrient concentrations in leaves are associated with their dynamic within the soil-plant system. Their availability in the soil is governed by pH, organic matter content, clay content, soil source rock, and, specifically for Fe and Mn, by the reduction potential (Li et al., 2007; Rengel, 2015). These factors can interfere with element uptake, thereby affecting leaf micronutrient concentrations.
For example, in CE, soil pH averaged 7.3, at which metal cations, such as Cu, Fe, Zn and Mn, as well as B, are considerably less available. In general, soil pH has a major impact on Mn availability in the soil (Marschner, 2012). Therefore, sufficient ranges established for ‘Prata-Anã’ were higher for Cu, Fe, Mn and Zn in CE compared with BA, but lower for B, which is associated with the higher fertility of soils in CE. However, a higher soil availability of Fe and Mn may cause temporary toxicity in plants in the case of heavy rain and may precipitate a rise in reducing conditions, especially in soils containing high Mn levels.
Sufficient concentration ranges obtained by the BLA for N, P, K, Mg, and S are highly consistent regardless of the site; however, the sufficient Ca concentration range proposed for CE (4.6-6.5 g kg−1) is broader than that determined for BA (5.3-5.8 g kg−1) due to higher Ca levels in soils in CE, 79.7 mmolc dm−3 compared to that in BA at 28.0 mmolc dm−3 (Table 1). Consecutive calcitic lime applications to soils in CE over the years are the reason for this discrepancy. Furthermore, in CE, the Ca/Mg ratio of 4.4:1 tends to result in a slight imbalance in the soil due to excessive Ca. The ideal soil Ca/Mg ratio for ‘Prata-Anã’ ranges from 1.5:1 to 3:1 (Silva, 2015). In BA, the Ca/Mg ratio is 2.5:1, thereby contributing to a higher Mg uptake.
The sufficient ranges established by MKmod were consistent for nearly all nutrients, and, in a number of cases, different from the sufficient range established by MKorig. The sufficient concentration ranges obtained by the BLA were more accurate (Table 5) owing to their lower estimated values, especially for N and K, the most accumulated nutrients in bananas (Hoffman et al., 2010; Deus et al., 2018a). This is consistent with decreases in the N and K fertilizer rates recommended for ‘Prata-Anã’ banana (Silva, 2015; Deus et al., 2018b).
The results highlight the importance of this study. The advantages of using the BLA to obtain sufficiency ranges include taking into account the site specificities, climate, soil, cultivar, and management, which increase the degree of precision in assessing the nutritional status of ‘Prata-Anã’ bananas by preventing miscalculated extrapolations.
Potential response curves and sufficiency ranges for leaf macro- and micronutrient concentrations and BIKW were established. They allow for an improved assessment of the nutritional status of fertigated ‘Prata-Anã’ bananas under different environmental conditions, which is a refinement to be incorporated into production systems.
Conclusions
The sufficiency ranges obtained by the BLA for ‘Prata-Anã’ banana in BA and CE, respectively, are: a) for macronutrients (g kg−1): N (19.3-22.0) and (19.9-22.1); P (1.4-2.0) and (1.4-1.6); K (22.6-32.2) and (24.0-31.3); Ca (4.6-6.5) and (5.3-5.8); Mg (1.8-2.6) and (2.1-2.7); S (1.3-2.0) and (1.3-1.5); b) for micronutrients (mg kg−1): B (8.4-13.0) and (13.7-16.4); Cu (5.6-8.4) and (4.4-5.2); Fe (54.2-77.6) and (39.0-55.0); Mn (140.1-222.8) and (64.0-91.0); Zn (13.5-18.3) and (12.4-14.5). The sufficiency ranges obtained by the BLA are more assertive when assessing the nutritional status for ‘Prata-Anã’ banana.
Acknowledgements
We would like to express our gratitude to Federal University of Viçosa and to the farms Sítio Barreiras for providing financial and logistical support to conduct the study. This work was carried out with the support of the Coordination for the Improvement of Higher Education Personnel - Brazil (CAPES) - Financing Code 001.
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Edited by
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Edited by: Anoop Kumar Srivastava
Publication Dates
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Publication in this collection
02 Apr 2021 -
Date of issue
2021
History
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Received
29 May 2020 -
Accepted
19 Oct 2020