Seeds were obtained from matrices originating from Embrapa Amazônia Oriental, Belém city, Pará State, Brazil, in which were washed for purpose of removing the pulp, and later sowed in a bed containing sand and sawdust mixture in a ratio of 3:1. Thirty days after sowing before the appearance of first two leaves, plants were transferred into black plastic bags with dimensions of 15 cm (width) × 25 cm (height), containing mixture of black earth, sawdust, and cattle manure in a ratio of 3:1:1, showing the following chemical characteristics: pH H 2 O 8.10; 53.00% (organic matter); 1.78% (N-total); 0.54% (P₂O₅); 1.07% (K₂O); 16.10 (C/N ratio); 2.96% (CaO); 0.48% (MgO); and 0.34% (S).

The experiment was conducted at Embrapa Amazônia Oriental, Belém city, Pará State, Brazil, during 200 days under greenhouse conditions with temperatures varying from 25˚C to 30˚C. Experimental design was a completely randomized design, with four replications and twelve treatments: nutritive solution containing all required macronutrient and micronutrients and in solutions with omission of N, P, K, Ca, Mg, S, B, Cu, Fe, Mn, and Zn, using the missing element technique, totaling 48 experimental plots. Table 1 shows the chemical composition of nutrient solution used in experiment.

At 10 months, when the plants reached approximately 20 cm in height, in which the roots were washed with distilled water to remove possible residues from the substrate, and then transplanted into the plastic pots with 10 L capacity, with a perforated base in order to facilitate the disposal and replacement of nutrient solution being used in experiment.

Plants were acclimatized for 60 days in Bolle-Jones [14] nutrient solution, used successfully in other researches with Amazonian crops under greenhouse conditions, modified and diluted to 1:10 [15] . Plants with a height of 50 cm were submitted to treatments with nutrient solution diluted to 1:1, total load with pH of ±5.5.

Nutrient solution were provided by percolation in plastic pots, with capacity for 10 L and renewed at 15 days. Daily, monitoring was carried out at solution level in collection bottles, completing them for 1 L per plant, when necessary adding distilled water.

During the experiment were collected leaf samples and description of symptoms

*Composition of solution A: 141.2 mg de H₃BO₃; 1750.0 mg de MnSO₄; 250.0 mg de CuSO₄∙5H₂O; 43.1 mg de MoO₃; 287.0 mg de ZnSO₄∙7H₂O, per liter of solution. **Composition of solution Fe-EDTA: 26.1 g de Na₂-EDTA; 89.2 g de NaOHN e 24.0 g de FeSO₄∙7H₂O, per liter of solution.

through photographs, until maximum visible manifestation of nutrient deficiency. Each plant was divided in leaves, stems, and roots and then dried in an oven with forced air circulation at 70˚C until reaching a constant mass. After, the samples were processed in a Willey mill for further chemical analysis of macronutrients and micronutrients levels in leaves, stems, and roots, according to methodology described by Malavolta [12] .

To calculate the relative growth rate (RGR) was used the equation:

RGR ( % ) = ( D .M .O .N . D .M .C .T . ) × 100

D.M.O.N. = dry mass of plant with nutrition omission;

D.M.C.T. = dry mass of plant in complete treatment.

Macronutrient and micronutrient levels in leaves, stems, and roots were submitted to analysis of variance, and means of treatments with omission of nutrients were compared with complete treatment using Dunnet test, at 5% probability, using the Assistat Software Version 7.7 [16] . From of means identified in Dunnet test were performed Figures following the methodology described by Nunes et al. [17] , in which consists of standardization of means founded in Dunnet test in function of different omissions.

Visual symptoms of nitrogen deficiency manifested 18^th days after the beginning of omission. Initially, older leaves gradually lost their green color from basal area, becoming yellow-green (Figure 1), with intensity of deficiency all the leaves showed yellowed (chlorotic), distributed in limbus, petiole and foliar veins.

The absorbed nitrogen is easily distributed in plants by phloem, in form of amino acids, thus, in deficiency the N of old leaves is redistributed to new leaves and organs of plants [15] [18] , justifying the beginning of chlorosis in old leaves. According to Carneiro et al. [19] , chlorosis is associated with N function in plant metabolism, since it is closely linked to carbon metabolism and to photorespiratory process, metabolic processes associated with photosynthesis.

Nitrogen omission interrupted the emission of new leaves, reducing the plant height (Figure 1). Batista et al. [20] observed in Annona muricata L., that nitrogen was the first visual symptom of manifested deficiency, in which the older leaves gradually lost green color, modifying in yellow with increased deficiency. Generalized chlorosis in older leaves and reduced plant height were characteristic symptoms in Theobroma grandiflorum with nitrogen deficient [21] .

The older leaves deficient in phosphorus showed dark green and bright coloration compared to complete treatment (Figure 1). In plant, the phosphorus deficiency promoted a reduction in plant height and in number and size of leaves (Figure 1). The symptoms presented in mangosteen occurred because the nutrient involved in various metabolic processes in plants, such as photosynthesis, respiration, gene transfer, energy transfer, synthesis of macromolecules, and active absorption of nutrients [11] . Symptoms of phosphorus deficiency observed in mangosteen were similar to obtained by Silva and Falcão [22] , and Frazão and Viégas [21] in tropical fruits (Bactris gasipaes Kunth, and Theobroma grandiflorum) in which observed reduction in plant height growth with omission of phosphorus.

The symptoms of potassium deficiency in mangosteen began with marginal chlorosis in older leaves, from the apex, expanding to central part between the veins, according to development of deficiency the leaf limb showed chlorosis, with necrosis on margins and leaf apices (Figure 1). Potassium omission in nutrient solution promoted negative effects on vegetative development of plant, observing a decrease in plant height, and number and leaf size (Figure 1).

Potassium deficient plants show paralysis in process of translocation of photoassimilates to drains, resulting in accumulation of carbohydrates in leaf tissue [23] , as well as reduction in photosynthetic efficiency promoted by decrease of conductance of mesophyll and lower capacity of fixation of CO₂ [24] . Similar symptoms of potassium deficiency manifesting chlorosis, followed by necrosis in apices and margins of old leaves, reduced in plant height were identified in Annona muricata [20] (Batista et al., 2003), and Myrciaria dubia [25] .

Calcium deficiency symptoms promote plant abnormalities, markedly characterized by reduced plant height and younger leaves, initially chlorosis along margins, remaining green leaf limb, however with intensity of deficiency results in an increase in chlorotic ranges (Figure 1). Reduction in plant height (Figure 1) and yellowing of younger leaves promoted by calcium omission were observed by Frazão and Viégas [21] in Theobroma grandiflorum and Viégas et al. [26] in Euterpe oleracea.

Calcium in plant tissue is characterized by low mobility, with limited redistribution in phloem [9] , in addition, calcium deficient plants show greater action of enzyme polygalacturonase, degrading the calcium pectates responsible for stability of membranes and cell walls [27] , justifying the first symptoms to be showed on younger leaves of plant.

The symptoms of magnesium deficiency in mangosteen were observed in older leaves of middle part of plant, with appearance of chlorosis between the veins from apex to center, remaining at base of green leaf (Figure 1). According to Hawkesford et al. [9] , symptoms of magnesium deficiency occurred initially in older leaves due to high mobility in phloem, being that chlorosis in leaves is related to nutrient function, since Mg constitutes the central atom of chlorophyll molecule, participates in structures of thylakoid membrane [28] .

Evolution of Mg deficiency promoted leaf senescence, reduced plant height and reduced number and size of mangosteen leaves (Figure 1). The symptoms of magnesium deficiency, chlorosis among the veins, were observed in Annona muricata [20] , Theobroma grandiflorum [21] , Bactris gasipaes Kunth [22] , and Euterpe oleracea [26] cultivated in Brazilian Amazon.

Sulfur-deficient in mangosteen plants showed on new leaves symptoms of yellowish-green coloration, with a lighter shade of color compared to leaves of complete treatment (Figure 1). Symptoms of sulfur deficiency are similar to nitrogen (sulfur is involved in composition of two essential amino acids, cystine and methionine, and in protein synthesis) [28] , however, sulfur has limited redistribution in phloem, thus, low translocation of nutrient from old leaves to new leaves [29] .

Symptoms of sulfur deficiency characterized by yellowing of younger leaves were observed in fruit trees, Annona muricata [20] , Theobroma grandiflorum [21] , Myrciaria dubia [25] , and Euterpe oleracea [26] , cultivated in Brazilian Amazon.

Boron: Boron deficiency in mangosteen was characterized by showing yellowish new leaves, twisted, atrophied, small, and thick leaves (Figure 1) promoted by absence of boron in lamella medial and cell wall through pectic connections between two complexes called rhamnogalacturonan [30] . According to intensity of symptoms caused the death of apical meristem, promoting sprouts, and stem of plants showed to be thicker, with greater diameter of stem. Symptoms of boron deficiencies showing the same characteristics were described in Euterpe oleracea [26] , Theobroma grandiflorum [31] , and Cocos nucifera [32] .

Copper: Copper deficiency initially manifested with yellowing of new leaves with pale green coloration between the veins. With increased symptoms, leaves showed deformed, narrow, with progression to central part (Figure 1). Enzymes polyphenoloxidase, ascorbate oxidase, and diamino oxidase are composed of copper, occurring in cell wall, playing a role in biosynthetic pathways of phenol, starting in quinone pathway until the formation of melanin and lignin, substances that increase the resistance to entry of pathogens. Thus, copper deficiency decreases the activity of enzymes (polyphenoloxidase, ascorbate oxidase, and diamino oxidase), promoting the accumulation of phenols and decrease in formation of lignin and melalines [33] .

Iron: Iron deficiency symptoms were first to manifest, less than 15^th days after initiation of treatments, showing that mangosteen is sensitive to iron deficiency. In leaf the symptoms were characterized by chlorosis in new leaves, veins with fine reticulate and yellowish background, remaining green vein. With increased deficiency, in plant observed an increase in number of shoots, while leaf showed completely yellowish, including vein, then necrosis from apex to center of leaf (Figure 1).

Iron in plant has function of maintaining the functional and structural integrity of thylakoid membrane, as well as essential for ferredoxin and chlorophyll biosynthesis, justifying high sensitivity of chloroplasts (chlorosis) and thylakoids to iron deficiency [11] . From results obtained in present study observed a reduction in plant height and leaf area compared to complete treatment, symptoms were similar to described by Moraes et al. [34] , studying nutritional limitations in mangosteen seedlings.

Manganese: The initial symptom of manganese deficiency in mangosteen was yellowing between veins with thick reticulate in newer leaves and bands of green tissue surrounding main vein. With evolution of symptoms of deficiency, leaves showed with chlorosis and smaller size. In general, manganese-deficient showed changes in chloroplasts with disarray of thylakoid cells and absence of stromal lamellae, since chloroplasts (site of occurrence of photosynthetic process) are organelles most sensitive to micronutrient deficiency [35] .

Zinc: Small and thin leaves with chlorotic areas between veins were symptoms of zinc deficiencies observed in new leaves of mangosteen (Figure 1). Zinc has a direct influence on carbohydrate metabolism [36] , as well as participates in metabolism of nitrogen, promoting accumulation of amino acids in plants deficient of zinc [37] .

With exception of zinc omission (in all variables) and copper omission (RDM and LDM) (Figure 2(a) and Figure 2(c)), other nutrient omissions limited the dry mass production compared to complete treatment (Table 2). The nutrients that most limited dry mass production (Figure 2(e)) in various parts of the plant

were iron, nitrogen, and sulfur. The reduction in total dry mass production with omission of nutrients were 94% (-Fe), 93% (-N), and 87% (-S).

According to Marschner [11] , iron is an important enzymatic activator as well as sulfur and nitrogen are nutrients constituent of formation of proteins being essential in metabolic activity, having a more structural function in plants. Iron limitation on mangosteen growth is not worrisome, because plantations of fruit tree are mostly established in Yellow Latosols, which have high levels of iron, considered as ferralitic soils. On the other hand, limitation on growth in nitrogen and sulfur should receive more attention due to limitation showed by soil.

The production of total dry mass in absolute values showed the following limiting order: Fe > N > S > K > B > Ca > P > Mg > Mn > Cu > Zn. Based on

+Significant and higher than complete treatment, by Dunnett test, at a 5% probability level; −Significant and less than complete treatment, by Dunnett test, at a 5% probability level; ^nsNot significant, by Dunnett test, at a 5% probability level.

complete treatment, highest dry mass production occurred on the leaves, followed by stem and roots.

The individual omissions of N, P, K, Ca, Mg, S, Cu, Fe, and Mn reduced the leaf level of their respective nutrient compared to complete treatment. The leaf level of boron also reduced with omission of micronutrient, but not significantly compared to complete treatment. Zinc omission showed a zinc leaf level similar to complete treatment.

Macronutrient level in complete treatment were in order N > K > Ca > S > P = Mg and, in micronutrients Fe > Mn > B > Zn > Cu. Based on leaves levels of macronutrients and micronutrients in mangosteens, following values are obtained in a first approximation: non-deficient (complete) and deficient (omission) values, respectively: N (16.4 and 12.5 g kg⁻¹); P (1.1 and 0.2 g kg⁻¹); K (10.2 and 8.1 g kg⁻¹); Ca (6.7 and 1.9 g kg⁻¹); Mg (1.1 and 0.1 g kg⁻¹); S (3.0 and 2.2 g kg⁻¹); B (20 and 16 mg kg⁻¹); Cu (7 and 3 mg kg⁻¹); Fe (266 and 86 mg kg⁻¹); Mn (58 and 17 mg kg⁻¹) (Table 3).

The individual omissions of N, P, K, Ca, Mg, Cu, Mn, and Fe reduced stem level of their respective nutrient compared to complete treatment, other omissions

+Significant and higher than complete treatment, by Dunnett test, at a 5% probability level; −Significant and less than complete treatment, by Dunnett test, at a 5% probability level; ^nsNot significant, by Dunnett test, at a 5% probability level.

did not differ. The decreasing order of macronutrient stem level of complete treatment were: N > K > Ca > S > P > Mg and, in micronutrients Fe > B > Mn > Zn > Cu. Macronutrient and micronutrient levels without deficiency (complete treatment) and deficiency (omissions) were respectively: N (11.4 and 8.3 g kg⁻¹); P (1.6 and 0.2 g kg⁻¹); K (11.3 and 1.7 g kg⁻¹); Ca (3.5 and 1.0 g kg⁻¹); Mg (0.3 and 0.1 g kg⁻¹); S (1.9 and 1.6 g kg⁻¹); B (15.5 and 13.0 mg kg⁻¹); Cu (8.3 and 5.1 mg kg⁻¹); Mn (13.3 and 2.4 mg kg⁻¹); Zn (11.1 and 8.4 mg kg⁻¹).

Regarding root content, omissions of all macronutrients and, Fe and Mn micronutrients reduced their respective levels, other omissions did not differ compared to complete treatment. The decreasing order of root level in macronutrients were N > K > P > Ca > S > Mg and, in micronutrients Fe > Zn > Cu > Mn > B. Macronutrient and micronutrient levels without deficiency (complete treatment) and deficiency (omissions) were respectively: N (13.1 and 9.0 g kg⁻¹); P (6.3 and 0.3 g kg⁻¹); K (11.8 and 2.2 g kg⁻¹); Ca (3.7 and 0.3 g kg⁻¹); Mg (0.7 and 0.1 g kg⁻¹); S (3.2 and 1.3 g kg⁻¹); B (16.0 and 13.4 mg kg⁻¹); Cu (28.5 and 24.6 mg kg⁻¹); Fe (1516.0 and 252.7 mg kg⁻¹); Mn (17.7 and 6.9 mg kg⁻¹).

From results obtained in complete treatment, extracting the parts of plant observed that highest N, Ca, Mg, B, Mn, and Zn levels were obtained in leaves, while of P, K, S, Cu, Fe, and Zn in roots. Lowest levels of macronutrients and micronutrients were observed in stem because it is a nutrient transporting organ.