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Growth, yield and nutrients of sweet cassava fertilized with zinc

Crescimento, produtividade e nutrientes da mandioca adubada com zinco

ABSTRACT:

The application of zinc fertilizers in the soil has been an agronomic practice to correct Zn deficiency in plants, aiming to increase productivity and/or nutritional quality. This study evaluated how zinc sulfate fertilization affects plant growth, yield performance and nutrient accumulation in the cassava ‘IAC 576-70’. The experimental design was in randomized blocks with eight replications. The treatments consisted of 0, 1.5, 3.0, 4.5 and 6.0 g p1-1 ZnSO4. Results showed improvement in yield with soil fertilization with ZnSO4, with the optimal dose of 2.5 g pl-1. The uptake of nutrients in plant parts is favored with lower doses of zinc fertilizer, with maximum points ranging from 0.8 to 3.2 g pl-1 for macronutrients and 1.6 to 3.6 g pl-1 for micronutrients. The Zn content in tuberous roots increases by more than 40% with fertilization up to 2.8 g pl-1 of fertilizer, which contributes to the nutritional value of roots.

Key words:
Manihot esculenta; fertilization; minerals; biofortification

RESUMO:

A aplicação de fertilizantes com zinco no solo tem sido uma prática agronômica para corrigir a deficiência de Zn nas plantas, visando aumentar a produtividade e/ou a qualidade nutricional. O objetivo deste estudo foi avaliar como a fertilização com sulfato de zinco afeta o crescimento da planta, o desempenho produtivo e o acúmulo de nutrientes na mandioca ‘IAC 576-70’. O delineamento experimental foi em blocos casualizados com oito repetições. Os tratamentos consistiram de 0, 1,5, 3,0, 4,5 e 6,0 g p1-1 ZnSO4. Os resultados mostraram melhoria no rendimento com a fertilização via solo com ZnSO4, com a dose ótima em 2,5 g pl-1. A absorção de nutrientes nas partes da planta é favorecida com menores doses de fertilizante de zinco, com pontos de máximo variando de 0,8 a 3,2 g pl-1 para macro e 1,6 a 3,6 g pl-1 para micronutrientes. O conteúdo de Zn nas raízes tuberosas tem aumento superior a 40% com a fertilização até 2,8 g pl-1 de fertilizante, o que contribui para o valor nutricional da mandioca.

Palavras-chave:
Manihot esculenta; adubação; minerais; biofortificação.

INTRODUCTION:

Cassava (Manihot esculenta Crantz) is a vital source of energy for both global food security and the Brazilian people. Cassava is an energy-dense food and; therefore, rated high for its caloric value, based on its carbohydrate content, providing 250 Kcal/ha/day compared to 200 Kcal/ha/day for corn, 176 Kcal /ha/day for rice, 114 Kcal/ha/day for sorghum and 110 Kcal/ha/day for wheat (EL-SHARKAWY, 2012EL-SHARKAWY, M. A. Stress-tolerant Cassava: The role of integrative ecophysiology-breeding research in crop improvement. Open Journal of Soil Science, v.2, p.162-186, 2012. Available from: <Available from: https://www.researchgate.net/publication/230635747_Stress-Tolerant_Cassava_The_Role_of_Integrative_EcophysiologyBreeding_Research_in_Crop_Improvement >. Accessed: Aug. 27, 2021. doi: 10.4236/ojss.2012.22022.
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; LEONEL et al., 2015LEONEL, M; et al. (Eds.). Culturas Amiláceas: batata-doce, inhame, mandioca e mandioquinha salsa. 1ª ed. Botucatu: CERAT/UNESP, p.183-326, 2015.; FAOSTAT, 2018FAOSTAT (Food and Agriculture Data). Produção, Área Colhida e Produtividade de Mandioca no Mundo. 2018. Available from: <Available from: http://www.fao.org/faostat/en/#data/QC >. Accessed: Apr. 08, 2021.
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; BAYATA, 2019BAYATA, A. Review on nutritional value of cassava for use as a staple food science. Journal of Analytical Chemistry, v.7, n.4, p.83-91, 2019. Available from: <Available from: https://www.researchgate.net/publication/337761959_Review_on_Nutritional_Value_of_Cassava_for_Use_as_a_Staple_Food >. Accessed: Aug. 17, 2022. doi: 10.11648/j.sjac.20190704.12.
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; BYJU & SUJA, 2020BYJU, G; SUJA, G. Mineral nutrition of cassava. Advances in Agronomy, v.159, p.169-235, 2020. Available from: <Available from: https://www.sciencedirect.com/science/article/abs/pii/S0065211319300926 >. Accessed: Sep. 21, 2021. doi: 10.1016/bs.agron.2019.08.005.
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).

The cassava crop requires adequate nutrition to maintain high production, as it absorbs large amounts of nutrients and exports around 1.27; 0.52; 3.02; 0.76; 0.60 and 0.36 kg t-1 of roots produced from N, P, K, Ca, Mg and S and 16.0; 1.51; 0.68; 2.23 and 2.43 g t-1 of Fe, Mn, Cu, Zn and B, respectively. Thus; although, it is considered a low fertility crop, the plant’s demands must be met by fertilizers at economically adequate levels (NGUYEN et al., 2002NGUYEN, H, et al. Effects of long-term nitrogen, phosphorus, and potassium fertilization on cassava yield and plant nutrient composition in North Vietnam. Journal of plant nutrition, v.25, p.425-442, 2002. Available from: <Available from: https://www.tandfonline.com/doi/abs/10.1081/PLN-120003374 >. Accessed: Nov. 10, 2021. doi: 10.1081/PLN-120003374.
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; LEONEL et al., 2015LEONEL, M; et al. (Eds.). Culturas Amiláceas: batata-doce, inhame, mandioca e mandioquinha salsa. 1ª ed. Botucatu: CERAT/UNESP, p.183-326, 2015.; EZUI et al., 2016EZUI, K. S; et al. Fertiliser requirements for balanced nutrition of cassava across eight locations in West Africa. Field Crops Research, v.185, p.69-78, 2016. Available from: <Available from: https://www.sciencedirect.com/science/article/abs/pii/S0378429015300642 >. Accessed: Aug. 10, 2021. doi: 10.1016/j.fcr.2015.10.005.
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).

Micronutrients play a central role in plant metabolism maintenance, growth and production, stress tolerance and disease resistance (SHAHZAD & AMTMANN, 2017SHAHZAD, Z.; AMTMANN, A. Food for thought: how nutrients regulate root system architecture. Current Opinion of Plant Biology, v.39, p.80-87, 2017. Available from: <Available from: https://www.sciencedirect.com/science/article/pii/S1369526616302254 >. Accessed: Aug. 23, 2022. doi: 10.1016/j.pbi.2017.06.008.
https://www.sciencedirect.com/science/ar...
). Zn is important for enzyme activation, regulation, and gene expression in plants, as well as protein synthesis, glucose metabolism, photosynthesis, phytohormones, fertility, growth regulation, seed development, and disease tolerance (TAIZ et al., 2017TAIZ, L; et al. Fisiologia e desenvolvimento vegetal. 6th. edn. Porto Alegre, Artmed, 2017. ISBN:9781605352558.; REHMAN et al., 2018REHMAN, A; et al. Zinc nutrition in wheat based cropping systems. Plant and Soil, v.422, p.283-315, 2018. Available from: <Available from: https://doi.org/10.1007/s11104-017-3507-3 >. Accessed: Aug. 17, 2022.
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; RAI et al., 2021RAI, S.; et al. Iron homeostasis in plants and its crosstem with copper, zinc, and manganese. Plant Stress, v.1, 100008, 2021.). LEKSUNGNOEN et al. (2022LEKSUNGNOEN, P.; et al. Biogeochemical cycling of zinc in soil-cassava cropping system in Thailand. Geoderma, v.406, 115496, 2022. Available from: <Available from: https://pubs.acs.org/doi/abs/10.1021/acs.est.5b05281 >. Accessed: Aug. 10, 2022. doi: 10.1016/j.geoderma.2021.115496.
https://pubs.acs.org/doi/abs/10.1021/acs...
) highlighted that the interaction between the soil Zn concentration and the cassava Zn concentration is poorly understood and that the Zn input from weathering is insufficient for the production of cassava.

Increases in Zn content in plants when subjected to various treatments involving this nutrient supplementation depend on genotypes, application methods, element concentration, and interactions with other elements (WHITE & BROADLEY, 2011WHITE, P. J; BROADLEY, M. R. Physiological limits to zinc biofortification of edible crops. Frontiers in Plant Science, 2:1-11, 2011. Available from: <Available from: https://www.frontiersin.org/articles/10.3389/fpls.2011.00080/full >. Accessed: Mar. 20, 2022. doi: 10.3389/fpls.2011.00080.
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; KACHINSKI, 2019KACHINSKI, W. W. Nutrição, produção e biofortificação agronômica com zinco em cultivares de feijoeiro-comum. 2019. 75p Dissertação (Mestrado) - Universidade do Centro-Oeste. Guarapuava.). Fertilizers such as ZnSO4, soluble in water, are often more efficient as their rapid release rapidly increases the concentration of Zn in the soil solution and this can result in greater plant uptake (MATTIELLO et al., 2021MATTIELLO, E. M.; et al. Efficiency of soil-applied 67Zn-enriched fertiliser across three consecutive crops. Pedosphere, v.31, n.4, p.531-537, 2021. Available from: <Available from: https://www.sciencedirect.com/science/article/abs/pii/S1002016020600443 >. Accessed: Aug. 23, 2021. doi: 10.1016/S1002-0160(20)60044-3.
https://www.sciencedirect.com/science/ar...
).

Appropriate Zn fertilization can promote growth by improving photosynthetic performance and chlorophyll synthesis, in addition to decreasing oxidative damage to the cell membrane induced by adverse environmental conditions. However, excess doses of Zn interfere with the absorption of essential elements and result in heavy metal toxicity (NATASHA et al., 2022NATASHA, N.; et al. Zinc in soil-plant-human system: A data-analysis review. Science of the Total Environment, v.808, p.152024, 2022. Available from: <Available from: https://www.sciencedirect.com/science/article/abs/pii/S004896972107100 X>. Accessed: Dec. 10, 2021. doi: 10.1016/j.scitotenv.2021.152024.
https://www.sciencedirect.com/science/ar...
).

Zinc deficiency in soil has increased the number of studies on agronomic biofortification of world food staple crops (VALENÇA et al., 2017VALENÇA, A. W.; et al. Agronomic biofortification of crops to fight hidden hunger in sub-Saharan Africa. Global Food Security, v.12, p.8-14, 2017. Available from: <Available from: https://doi.org/10.1016/j.gfs.2016.12.001 >. Accessed: Aug. 17, 2022.
https://doi.org/10.1016/j.gfs.2016.12.00...
). JOY et al. (2015JOY, E. J. M.; et al. Zinc-enriched fertilisers as a potential public health intervention in Africa. Plant Soil, v.389, n.1-2, p.1-24, 2015. Available from: <Available from: https://link.springer.com/content/pdf/10.1007/s11104-015-2430-8.pdf >. Accessed: Aug. 11, 2022.
https://link.springer.com/content/pdf/10...
) modelled the potential of Zn-enriched fertilizers to alleviate dietary Zn deficiency, focusing on ten African countries with zinc deficiency. Their results showed that agronomic biofortification can increase the amount of absorbable Zn in the diet by 5%.

Micronutrient deficiencies (hidden hunger) have become a silent epidemic and inadequate Zn intake is quite substantial, affecting approximately two billion people worldwide, most of them pregnant women and children. Zn deficiency can cause anemia, dermatitis, growth retardation, affect reproductive capacity and mental function, with results showing that zinc supplementation reduced the incidence of diarrhea and respiratory infections in children (WESSELLS & BROWN, 2012WESSELLS, K. R.; BROWN, K. H. Estimating the global prevalence of zinc deficiency: results based on zinc availability in national food supplies and the prevalence of stunting. PLoS One, v.7, e50568, 2012. Available from: <Available from: https://journals.plos.org/plosone/article/file?id=10.1371/journal.pone.0050568&type=printable >. Accessed: Aug. 16, 2022. doi: 10.1371/journal.pone.0050568.
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; LIVINGSTONE, 2015LIVINGSTONE, C. Zinc: Physiology, deficiency, and parenteral nutrition. Nutrition in Clinical Practice, v.30, p.371-382, 2015. Available from: <Available from: https://doi.org/10.1177/0884533615570376 >. Accessed: Aug. 18, 2022.
https://doi.org/10.1177/0884533615570376...
; OKWUONU et al., 2021OKWUONU, I. C.; et al. Opportunities and challenges for biofortification of cassava to address iron and zinc deficiency in Nigeria. Global Food Security, v.28, e100478, 2021. Available from: <Available from: https://doi.org/10.1016/j.gfs.2020.100478 >. Accessed: Aug. 17, 2022.
https://doi.org/10.1016/j.gfs.2020.10047...
).

Given the importance of cassava as a staple food crop and the need for a balanced approach to Zn fertilization to achieve increased food production in a sustainable and responsible manner, this study verified how ZnSO4 doses affect plant growth, yield performance and nutrient absorption in the sweet cassava ‘IAC 576-70’.

MATERIALS AND METHODS:

The experimental study was done in Botucatu, in the state of São Paulo, Brazil. The geographic coordinates are 22º59’ S; 48º30’ W, with an altitude of 778 meters above sea level.

The soil used in the study was a dystrophic Red Latosol with a sandy texture sampled at a depth of 20 cm. Soil chemical characteristics before experiment planting were: pH (CaCl2): 5.1; M.O (g dm-3): 10.0; Presin (mg dm-3): 6.0; H+AL (mmolc dm-3): 14.0; K (mmolc dm-3): 1.1; Ca (mmolc dm-3): 11.0; Mg (mmolc dm-3): 5.0; CTC (mmolc dm-3): 31.0; base saturation (%): 55.0; Fe (mg dm-3): 5.0; Cu (mg dm-3): 0.4; Mn (mg dm-3): 2.2; B (mg dm-3): 0.1 and Zn (mg dm-3): 0.4. Soil Zn contents are considered low for cassava (Zn < 0.6 mg dm-3) (LORENZI et al., 1997LORENZI, J. O; et al. Raízes e tubérculos. In: RAIJ, B. van.; CANTARELLA, H.; QUAGGIO, J.A.; FURLANI, A. M. C., ed. Recomendações de adubação e calagem para o Estado de São Paulo. Campinas: Instituto Agronômico de Campinas, p.221-229, 1997. (Boletim Técnico, 100).).

The experiment was conducted in a randomized block design with eight replications. Zinc sulfate (ZnSO4 7H2O with 20% of zinc) was employed as the zinc source, and five doses of ZnSO4 were applied: 0, 1.5, 3.0, 4.5, and 6.0 g pl-1. A 310 L plastic box containing a cassava plant was used to represent each plot. The plants were spaced at a distance of 1.00 × 1.5 m (Figure 1).

Figure 1
Image of the installation of the experiment and cassava plants.

For cassava planting, the soil was first poured into 310 L boxes with a height of 0.54 m and a diameter of 1.04 m. In the planting fertilization was used 100 g pl-1 P2O5, 25 g pl-1 K2O, and 0.88 g pl-1 boron. As sources of P, K and B were used simple superphosphate (18% P2O5), potassium chloride (60% K2O) and boric acid (17% B) fertilizers.

Pits were opened for fertilizing, and fertilizers were poured into the pits’ soil. After that, one cassava stem cutting was planted horizontally in each pit and manually filled with dirt. Cassava stem cutting with 15 cm in length were obtained from the middle third of 12-month-old plants. The planting was completed on April 25, 2019. Nitrogen was applied using urea (45% N) at 35 days after planting (DAP) at a rate of 13.64 g pl-1 (equivalent to 40 kg ha-1).

The crop was irrigated using a drip irrigation system, which met the crop’s water need. The pests and disease control was carried out in accordance with the requirements and technical guidelines. The plants were harvested at 368 DAP.

The number of stems and leaves per plant was determined by counting. The diameter of the stems was measured at a height of 10 cm from the soil surface. Plant height was determined from the soil surface to the highest point of the plant. The length of the roots was measured from one end to the other and the diameter was determined in the region of the middle third with a caliper.

Plant parts were weighed to obtain fresh matter values. Then, samples of fresh material were dehydrated in an oven with forced air circulation at 65 °C until reaching constant weight. After drying, the material was weighed and the dry matter accumulated in each part of the plant was calculated.

The N concentration in the plant tissues was determined by sulfuric acid (H2SO4) digestion and quantified using the semi-micro-Kjeldahl method. P, K, Ca, Mg, S, Cu, Fe, Mn, and Zn concentrations were determined by atomic absorption spectrophotometry after nitric acid (HNO3) - perchloric acid (HClO4) digestion (MALAVOLTA et al., 1997MALAVOLTA, E; et al. Avaliação do estado nutricional das plantas: princípios e aplicações. 2. ed. Piracicaba: Associação Brasileira de Potassa e do Fósforo. 319p., 1997. Available from: <Available from: https://www.infraestruturameioambiente.sp.gov.br/institutodebotanica/1997/01/avaliacao-do-estado-nutricional-das-plantas-principios-e-aplicacoes/ >. Accessed: May, 23, 2022.
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).

The amounts of accumulated nutrients in each plant organ were calculated by multiplying the concentrations of nutrients by the accumulated amount of dry matter in each plant organ.

The data were submitted to analysis of variance in order to perform the statistical analysis. Regression analysis was used to assess the effect of ZnSO4 doses (P ≤ 0.05). The highest value of the coefficient of determination was used as the criterion for selecting the linear or quadratic model (R2) (P ≤ 0.05). Sisvar software was used for statistical analysis, while Excel was used to create graphics.

RESULTS AND DISCUSSION:

The growth parameters were influenced by the doses of ZnSO4 tested in the cultivation of cassava ‘IAC 576-70’ (Figure 2). Cassava plants had an increase in the height of the main stem with zinc fertilization. Stem diameter and number of leaves increased with maximum points at doses of 2.7 and 2.8 g pl-1, respectively. The number of roots per plant was positively affected by ZnSO4 fertilization, but shorter roots were produced.

Figure 2
Plant height, leaf number, stem diameter, stem number, number of roots, root length, root diameter and yield of sweet cassava plants in response to ZnSO4 fertilizer (*P < 0.05, ** P < 0.01).

The effects of zinc fertilization on growth parameters are due to the fundamental roles of this nutrient in numerous biochemical pathways of plants, such as auxin, which is a growth regulator (AIRES, 2009AIRES, C. B. Zinco, fator fundamental para aumento e melhora da produção agrícola. 2009. Available from: <Available from: https://www.agrolink.com.br/noticias/zinco--fator-fundamental-para-aumento-e-melhora-da-producao-agricola_94756.html >. Accessed: May, 31, 2021.
https://www.agrolink.com.br/noticias/zin...
).

Fertilization with ZnSO4 interfered with the accumulation of dry matter (DM) in parts of the cassava plant, with the exception of the seed stem. The total amount of dry matter accumulated in the plant increased up to the dose of 2.8 g pl-1, with a decrease at higher doses (Figure 3).

Figure 3
Dry matter accumulation in parts of sweet cassava plants in response to ZnSO4 fertilizer (*P < 0.05, ** P < 0.01).

CAMPOS (2000CAMPOS, M F. , Desenvolvimento da planta de mandioca em função da calagem e adubação com zinco. 2000. Dissertação (Mestrado), Botucatu, São Paulo.70p.) discovered that a dose of 2.04 g pl-1 ZnSO4 enhanced the DM of tuberous roots and MALAVOLTA et al. (1997MALAVOLTA, E; et al. Avaliação do estado nutricional das plantas: princípios e aplicações. 2. ed. Piracicaba: Associação Brasileira de Potassa e do Fósforo. 319p., 1997. Available from: <Available from: https://www.infraestruturameioambiente.sp.gov.br/institutodebotanica/1997/01/avaliacao-do-estado-nutricional-das-plantas-principios-e-aplicacoes/ >. Accessed: May, 23, 2022.
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) explained that the reduction in the production of DM in plants subjected to high levels of zinc is due to the accumulation of plugs containing Zn in the xylem of plants, which hinder the rise of crude sap.

Yield was positively affected by fertilization with ZnSO4, with a maximum point at 2.8 g pl-1.

Zinc is a cation that interacts with almost all plant nutrients present in the soil, especially anions. REHMAN et al. (2018REHMAN, A; et al. Zinc nutrition in wheat based cropping systems. Plant and Soil, v.422, p.283-315, 2018. Available from: <Available from: https://doi.org/10.1007/s11104-017-3507-3 >. Accessed: Aug. 17, 2022.
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) reported that Zn interacts positively with N, K, Mg, and negatively with P, Mn and B.

The fertilization of sweet cassava with ZnSO4 pronouncedly affected the accumulation of macronutrients in the plant shoot (leaves and stems), but with an effect on the accumulation of N, P, K, Ca and Mg in the tuberous roots. In general, the use of high doses of ZnSO4 in the fertilization of cassava ‘IAC 576-70’ decreased the accumulation of macronutrients in the plant parts, with variations in the maximum accumulation points among the nutrients (Figures 4 to 6).

Figure 4
Nitrogen (N) and phosphorus (P) accumulation in parts of sweet cassava plants in response to ZnSO4 fertilizer (*P < 0.05, **P < 0.01).

The accumulation of N in the leaf was higher up to the estimated dose of 2.6 g pl-1 ZnSO4, it was greater in the stem until 0.8 g pl-1 ZnSO4, with a decline beyond these doses, and it had a linear decline in seed stem (Figure 4). Plant productivity is largely determined by the interaction between carbon and N metabolism, with N assimilation resulting directly or indirectly from photosynthesis. The role of zinc in these processes can be seen in the effect of doses on N accumulation in leaves and stems, when higher doses had a negative effect on this nutrient. In addition, the toxic effect of zinc on chlorophyll can be observed indirectly by N, since 50% of the total N in leaves is part of the chloroplast and leaf chlorophyll compounds (CHAPMAN & BARRETO, 1997CHAPMAN, S. C.; BARRETO, H. J. Using a chlorophyll meter to estimate specific leaf nitrogen of tropical maize during vegetative growth. Agronomy Journal, v.89, n.1, p.557-562, 1997. Available from: <Available from: https://acsess.onlinelibrary.wiley.com/doi/10.2134/agronj1997.00021962008900040004x >. Accessed: Aug. 13, 2021. doi: 10.2134/agronj1997.00021962008900040004x.
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).

KUTMAN et al. (2011KUTMAN, U. B.; et al. Effect of nitrogen on uptake, remobilization and partitioning of Zn and Fe throughout the development of durum wheat. Plant and Soil, v.342, p.149-164, 2011. Available from: <Available from: https://link.springer.com/content/pdf/10.1007/s11104-010-0679-5.pdf >. Accessed: Aug. 18, 2022.
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) reported a positive relationship between N and Zn in plants, with N increasing the uptake of Zn by the roots, as well as its translocation to the shoot.

The accumulation of P in the leaf, stem, and tuberous root was usually larger than the control, with the maximum accumulation at 2.5, 1.4, and 3.2 g pl-1 ZnSO4 dose, respectively (Figure 4).

The accumulation of K in the leaf, stem and tuberous root followed a similar pattern, being higher than the control and decreasing after ZnSO4 doses of 2.9, 2.1, and 2.5 g pl-1, respectively (Figure 5).

Figure 5
Potassium (K) and calcium (Ca) accumulation in parts of sweet cassava plants in response to ZnSO4 fertilizer (*P < 0.05, **P < 0.01).

Regardless of the levels of zinc sulphate fertilization, the aerial part of cassava (stem and leaves) showed the highest calcium accumulations, with effect of fertilization levels on the accumulation of this nutrient in leaves, seed stems and tuberous roots (Figure 5). Increasing levels of zinc fertilization increased Ca accumulation in leaves with decrease at the highest dose. The accumulation of Ca decreased in the seed stem with increasing fertilization. Increased accumulation in roots was observed only at the lowest dose. These results showed the reduction of Ca availability under high doses of ZnSO4, as reported by PRASAD et al. (2014PRASAD, R.; et al. Agronomic biofortification of cereal grains with iron and zinc. Advances in Agronomy, v.125, p.55-91, 2014. Available from: <Available from: https://doi.org/10.1016/B978-0-12-800137-0.00002-9 >. Accessed: Aug. 18, 2022.
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).

Mg in the leaf, stem, root, and S in stem and root all behaved the same way, being greater than control and decreasing with doses of 2.7, 2.6, 2.1, and 2.6 g pl-1 ZnSO4, respectively (Figure 6). The lower concentration of Mg might be due to the physiological response of the plant to the highest Zn concentration in solution, which may have affected the uptake system and thus lowered the apparent concentration.

Figure 6
Magnesium (Mg) and sulphur (S) accumulation in parts of sweet cassava plants in response to ZnSO4 fertilizer (*P < 0.05, **P < 0.01).

The effects of zinc fertilization on micronutrients were variable among nutrients and for each nutrient among plant parts. Data analysis revealed that ZnSO4 doses had no effect on Cu in cassava leaves. Doses had no influence on the accumulation of Zn and Mn in the seed stem (Figure 7).

Figure 7
Iron (Fe) and manganese (Mn) accumulation in parts of sweet cassava plants in response to ZnSO4 fertilizer (*P < 0.05, **P < 0.01).

In the aerial part of cassava plants, the increase in the levels of zinc fertilization increased the accumulation of iron (Fe); however, with decreases in the highest doses. For the seed stem and tuberous roots, decreases in iron accumulation were observed with fertilization (Figure 7). The decrease of Fe may be due to competitive interactions with Zn, which probably occur at the absorption sites of plant roots.

Mn had the greatest accumulation in leaves and stems (Figure 6), as Mn is preferentially reported to the plant shoot, to act in the photosynthetic processes of the plant (TAIZ et al., 2017TAIZ, L; et al. Fisiologia e desenvolvimento vegetal. 6th. edn. Porto Alegre, Artmed, 2017. ISBN:9781605352558.).

Fertilization with MnSO4 negatively affected the accumulation of manganese in tuberous roots (Figure 7). The adverse relationship between Zn and Mn was also described by BARBEN et al. (2010BARBEN, S. A.; et al., Phosphorus and manganese interactions and their relationships with zinc in chelator-buffered solution grown russet Burbank potato. Journal of Plant Nutrition, v.33, n.5, p.752-769, 2010. Available from: <Available from: https://www.tandfonline.com/doi/abs/10.1080/01904160903575964 >. Accessed: Nov. 03, 2021. doi: 10.1080/01904160903575964.
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) who observed that Mn concentrations in potato plant tissues decreased with increasing Zn concentration in the nutrient solution. VADLAMUDI et al. (2020VADLAMUDI, K.; et al. Influence of zinc application in plant growth: an overview. European Journal of Molecular & Clinical Medicine, v.7, p.2321-2327, 2020. Available from: <Available from: https://ejmcm.com/article_4916_6e8f59981b32c36fd8a3ec316a5a1329.pdf >. Accessed: Aug. 18, 2022.
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) discussed that excess zinc usually affects the absorption of P, Fe and Mn, causing structural deficiencies in the plant.

In the absence of ZnSO4, copper (Cu) accumulation was higher in the seed stems; although, the maximal accumulation in the stem was higher up to the estimated dose of 2.1 g pl-1 of ZnSO4 (Figure 8). Cu is a key micronutrient for crops because it regulates enzymatic activity in shoot tissues’ photosynthetic and respiratory functions (KIRKBY & RÖMHELD, 2007KIRKBY, E. A; RÖMHELD, V. Micronutrientes na fisiologia de plantas: funções, absorção e mobilidade. Piracicaba: International Plant Nutrition Institute, 2007. (Encarte técnico informações agronômicas, 18). Available from: <Available from: http://www.ipni.net/publication/ia-brasil.nsf/0/8A79657EA91F52F483257AA10060FACB/$FILE/Encarte-118.pdf >. Accessed: Mar. 08, 2021.
http://www.ipni.net/publication/ia-brasi...
). SAMREEN et al. (2017SAMREEN, T.; et al. Zinc effect on growth rate, chlorophyll, protein and mineral contents of hydroponically grown mung beans plant (Vignar adiata). Arabian Journal of Chemistry, v.10, S1802-1807, 2017. Available from: <Available from: https://doi.org/10.1016/j.arabjc.2013.07.005 >. Accessed: Aug. 17, 2022.
https://doi.org/10.1016/j.arabjc.2013.07...
) suggested that both Cu and Zn are absorbed through same mechanism and might suppress the other if one is present in excess.

Figure 8
Cooper (Cu) and zinc (Zn) accumulation in parts of sweet cassava plants in response to ZnSO4 fertilizer (*P < 0.05, **P < 0.01).

Zinc uptake depends on the different types of plant species as mainly depends upon the concentration and composition of media. Zinc translocation happens through the symplast and apoplast from roots to plant tissue (TAIZ et al., 2017TAIZ, L; et al. Fisiologia e desenvolvimento vegetal. 6th. edn. Porto Alegre, Artmed, 2017. ISBN:9781605352558.).

Zn is absorbed predominantly as Zn2+, and soil texture, pH, organic matter, microbial activity and concentrations of P and cationic elements affect the availability of Zn for plant absorption (ALLOWAY, 2009ALLOWAY, B. J. Soil factors associated with zinc deficiency in crops and humans. Environmental Geochemistry and Health, v.31, p.537-548, 2009. Available from: <Available from: https://link.springer.com/content/pdf/10.1007/s10653-009-9255-4.pdf >. Accessed: Aug. 12, 2022.
https://link.springer.com/content/pdf/10...
; BROADLEY et al., 2012BROADLEY, M.; et al. Function of Nutrients: Micronutrients. In: MARSCHNER, P. (ed.). Marschner’s Mineral Nutrition of Higher Plants. Elsevier Ltd, p.191-248, 2012.). The accumulation of Zn in the parts of the plant was influenced by fertilization, with the exception of the accumulation in the seed stem (Figure 8).

Zinc contents were higher in the shoot cassava parts. According to LEKSUNGNOEN et al. (2022LEKSUNGNOEN, P.; et al. Biogeochemical cycling of zinc in soil-cassava cropping system in Thailand. Geoderma, v.406, 115496, 2022. Available from: <Available from: https://pubs.acs.org/doi/abs/10.1021/acs.est.5b05281 >. Accessed: Aug. 10, 2022. doi: 10.1016/j.geoderma.2021.115496.
https://pubs.acs.org/doi/abs/10.1021/acs...
), Zn concentrations vary between cassava cultivars and plant parts, with shoot biomass being more abundant in Zn than below ground biomass. In their study, the results showed that 88% of the total Zn absorption was accumulated in the shoot of the cassava plant.

The amount of Zn in the tuberous roots increased until the estimated dose of 2.8 g pl-1 ZnSO4, after which the amount of Zn accumulated in the tuberous roots reduced (Figure 8). It is important to note that the 41.62% increase in zinc accumulated in cassava tuberous roots indicates possibilities for agronomic biofortification.

GARCIA-BANUELOS et al. (2014GARCIA-BANUELOS, M. L. et al. Biofortification - promising approach to increasing the content of iron and zinc in staple food crops. Journal of Elementology, v.19, n.3, p.865-888, 2014. Available from: <Available from: https://doi.org/10.5601/jelem.2014.19.3.708 >. Accessed: Aug. 12, 2022.
https://doi.org/10.5601/jelem.2014.19.3....
) discussed that; although, food fortification and supplementation are the most commonly used strategies to alleviate micronutrient deficiencies, agronomic biofortification is potentially easy, cost-effective, efficient and applicable to most crops.

Zinc deficiency in humans is largely due to inadequate intake or absorption of zinc from the diet. This mineral deficiency affects about a third of the world population and leads to physiological disorders that affect the immune, gastrointestinal, epidermal, central nervous, skeletal and reproductive systems (ROOHANI et al., 2013ROOHANI, N., et al. Zinc and its importance for human health: an integrative review. Journal of Research in Medical Science, v.18, p.144-157, 2013. Available from: <Available from: https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3724376/pdf/JRMS-18-144.pdf >. Accessed: Aug. 17, 2022.
https://www.ncbi.nlm.nih.gov/pmc/article...
).

CONCLUSION:

Soil fertilization with zinc sulphate increased the number of tuberous roots per plant, with an increase in dry matter accumulation and yield; however, excess Zn impaired cassava growth. The best dose to maximize root production is 2.5 g pl-1, with estimated doses ranging from 0.8 to 3.2 g pl-1 of ZnSO4 for greater macronutrient accumulation and 1.6 to 3.6 g pl-1 of ZnSO4 for the highest accumulations of micronutrients in the whole plant. The positive response of Zn accumulation in sweet cassava leaves and roots can be better explored in studies aiming at agronomic biofortification.

ACKNOWLEDGMENTS

This work was supported by the Conselho Nacional de Desenvolvimento Científico e Tecnológico (CNPq) (Grant numbers 302827/2017-0 and 302848/2021-5) and was financed in part by the Coordenação de Aperfeiçoamento de Pessoal de Nível Superior (CAPES), Brasil - Finance code 001.

REFERENCES

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    CR-2022-0064.R1

Edited by

Editors: Leandro Souza da Silva(0000-0002-1636-6643) Jackson Kawakami(0000-0003-2422-1564)

Publication Dates

  • Publication in this collection
    13 Jan 2023
  • Date of issue
    2023

History

  • Received
    08 Feb 2022
  • Accepted
    15 Sept 2022
  • Reviewed
    28 Nov 2022
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