Calcium Biofortiﬁcation of Rocha Pear Fruits: Implications on Mineral Elements, Sugars and Fatty Acids Accumulation in Tissues

: Following an agronomic approach for the Ca enrichment of Rocha pears, this study aimed to assess the interactions between mineral nutrients in fruit tissues at harvest and after storage for 5 months and to characterize the implications on the proﬁle of sugars and fatty acids (FA). A total of seven foliar sprays (with concentrations of 0.1–0.6 kg · ha − 1 Ca(NO 3 ) 2 and 0.8–8 kg · ha − 1 CaCl 2 ) were applied to pear trees. After harvest, the fruits were stored for 5 months, in environmentally controlled chambers, and the mineral contents in ﬁve regions (on the equatorial section) of the fruits were assessed, while the sugar and FA content were quantiﬁed. For both dates, all foliar sprayed treatments, at different extends, increased Ca content in the center and near the epidermis of Rocha pear fruits and the levels of K, Mn, Fe, Zn and Cu also varied. At harvest, the Ca treatments did not affect the levels of sucrose, glucose, fructose and sorbitol and, after storage, their concentrations remained higher in Ca-treated fruits. Additionally, the tendency of the relative proportions of FA was C18:2 > C18:1 > C16:0 > C18:3 > C18:0 > chains inferior to 16 C (<16:0), but after storage it was C18:2 > C16:0 > C18:3 > C18:0 > C18:1 > chains inferior to 16 C (<16:0). It is concluded that the heterogeneous distribution of Ca in the tissues of Rocha pear fruits results from its absorption in the peel after Ca(NO 3 ) 2 and CaCl 2 sprays and from the xylemic ﬂux in the core prior to maturity. Additionally, the hydrolysis of complex polysaccharides affects the contents of simpler sugars during maturation, ripening and senescence, while storage decreases the amount of total fatty acids (TFA), but the double bond index (DBI) indicate that cell membrane ﬂuidity remains unaffected.


Introduction
A deficient Ca intake from one's diet affects half the global population [1], leading to a progressive loss of bone mass, favoring the development of pathologies such as osteopenia, which, when aggravated, can be diagnosed as osteoporosis [2,3]. In children, despite vitamin D deficiencies being the main cause, Ca-mediated deformities such as rickets can also occur [4]. Calcium intake varies with age or gender, being required in quantities higher than 100 mg/day [5]. A study by Cormick and Belizán (2019) [6] compiled information from four different sources (SACN, IOM, EFSA and the WHO-from the United Kingdom, the United States of America and Canada, Europe and the FAO) and showed that the recommended daily values varied between 200 to 1300 mg (presenting differences even when considering the individual's same characteristics). It further indicated for adults (over 19 years old) an average daily intake of Ca between 800-1300 mg [6] but, over a long period of time, the daily intake should not exceed 2000-3000 mg to avoid compromises in health [6,7].
Plant biofortification focuses on the increase in a target mineral in the edible part of a chosen genotype. This can be achieved by different strategies, such as DNA modification (the transgenic approach), the selection of favorable characteristics (the breeding approach) or the use of foliar/soil fertilizers (the agronomic approach) [8]. According to Garg et al. (2018) [9], transgenic, breeding and agronomic approaches prevail in cereals and, although the mineral enrichment of fruits might be carried out with the three approaches, fruits present the lesser number of studies in both agronomic and breeding techniques. However, relative to fruits and other vegetables, the content of Ca in cereals is low (e.g., to meet daily Ca needs in adults, a diet exclusively with cereals could imply the intake of up to 10 kg) [10]. Additionally, food products with lower contents of antinutrients are preferable, as the presence of phytates and oxalates can affect the bioavailability of Ca [10][11][12]. In fact, the level of phytic acid is higher in cereals, oilseeds and legumes (on a dry weight basis varying between 1-5%), in comparison to other vegetables and fruits such as carrots or bananas (on a dry weight basis varies between 0.015-0.09%) [13]. Oxalates also prevail in fruits such as kiwi, avocado or oranges (about 16-29 mg per portion), in comparison to other fruits such as pears (which ranges between 1-3 mg) [14].
Pre-harvest factors (such as mineral nutrition, chemical treatments, agronomic practices or climacteric aspects) affect the post-harvest quality and physiology of fruits, as at that point quality can only be maintained but not improved [15]. Yet, the enrichment of several fruits, namely pears, with foliar applications of Ca (during the pre-harvest phase), besides increasing the amounts of this nutrient, maintains its quality during storage and triggers some positive changes in the organoleptic properties, such as aroma [16][17][18][19][20][21][22]. Nevertheless, the mineral content of pears varies according to the variety [23,24], being its sweetness related to the content of sugars, namely sorbitol, glucose, fructose and sucrose [23,24]. Additionally, lipids, although present in low quantities (with contents varying according to the storage method), are not just linked to the membrane structure of cells, but also to the biosynthesis of aroma volatiles [24][25][26].
Rocha pear is a Portuguese variety that can be stored in environmentally controlled chambers, at least up till seven to eight months, while it is also resistant to handling and transport, allowing its marketability to consumers for most of the year (e.g., about 8 months after harvest) [27]. As Rocha pear is a climacteric fruit, storage conditions are thus crucial, since it persists in being physiologically active during the post-harvest period [28]. Following an agronomic approach for the Ca enrichment of Rocha pears, this study aimed to assess the interactions among mineral nutrients in the fruit tissues between harvest and storage for 5 months and to assess the related profile of sugars and fatty acids (FA). Thus, quality modifications in Rocha pear fruits resulting from Ca increases in fruit tissues was assed to determine eventual changes in other minerals localization, as well as in some related nutritional aspects.

Experimental Design
In an orchard located in Portugal (GPS coordinates 39 •  (Pyrus communis L.). For the first two foliar applications, different sets of trees (four trees per set) were sprayed with 0.1 and 0.6 kg·ha −1 Ca(NO 3 ) 2 and 0.8 and 1.6 kg·ha −1 CaCl 2 (corresponding to treatments T0.1 and T0.6, as well as T0.8 and T1.6, respectively). Another set (twelve trees) was kept as the control, only being applied water without any other fertilizers. For the subsequent third and the remaining 4 foliar applications, respectively, 4 and 8 kg·ha −1 of CaCl 2 were applied to all the four sets. Water accumulation from rainfall during the foliar application period reached 60.4 mm, with an average value of 0.41 mm, reaching a daily maximum of 18.03 mm. Temperatures varied between 6 • C and 41 • C, with minimum and maximum mean values of 15 • C and 23 • C, respectively. The fruits were harvested on 10 September and each treatment was stored in environmentally controlled chambers (at −0.5-1 • C and 95% humidity). An analysis of the stored samples occurred on 13 March 2019.

Mineral Elements Content in Fruits
Quantitative determinations of Ca, K, Mn, Fe, Zn and Cu in fruits were assessed by using a micro-Energy Dispersive X-ray-Fluorescence system (µ-EDXRF) (M4 Tornado TM Bruker, Germany) as described in   [29], with adaptations regarding sample preparation. Fruits were firstly cleaned with deionized water and then horizontally sliced at the equatorial zone with a stainless-steel blade. The slices were dried at 60 • C until constant weight ( Figure 1). An example of the different zones is present in Figure 1. communis L.). For the first two foliar applications, different sets of trees (fou were sprayed with 0.1 and 0.6 kg·ha −1 Ca(NO3)2 and 0.8 and 1.6 (corresponding to treatments T0.1 and T0.6, as well as T0.8 and T1.6, Another set (twelve trees) was kept as the control, only being applied wate other fertilizers. For the subsequent third and the remaining 4 foliar respectively, 4 and 8 kg·ha −1 of CaCl2 were applied to all the four sets. Water from rainfall during the foliar application period reached 60.4 mm, with an of 0.41 mm, reaching a daily maximum of 18.03 mm. Temperatures varied and 41 °C, with minimum and maximum mean values of 15 °C and 23 °C The fruits were harvested on 10 September and each treatment w environmentally controlled chambers (at −0.5 °C-1 °C and 95% humidity). the stored samples occurred on 13 March 2019.

Mineral Elements Content in Fruits
Quantitative determinations of Ca, K, Mn, Fe, Zn and Cu in fruits we using a micro-Energy Dispersive X-ray-Fluorescence system (µ-EDXRF) (M Bruker, Germany) as described in   [29], with adaptati sample preparation. Fruits were firstly cleaned with deionized wa horizontally sliced at the equatorial zone with a stainless-steel blade. The sli at 60 °C until constant weight ( Figure 1). An example of the different zone Figure 1. Example of a sliced sample of Rocha pear fruits with a stainless-steel bla delineate different zones for minerals assessment (from center to epidermis, respectively).

Sugar Content in Fruits
Sugar extraction followed the procedure of Medlicott and Thompson total of fifteen pears per treatment (n = 3, thus 5 fruits per sample) were with deionized water and then peeled, followed by a longitudinal cut. A t pulp (8 g per fruit) per sample was added to 150 mL of cold ultrapure water followed by the addition of ultrapure water until 200 mL. Samples were ke were transferred to ultrasounds (for 5 min) and were later centrifuged (15,0 °C). The supernatant was transferred to glass tubes in ice, while th resuspended in ultrapure water following a new centrifuge in the same co supernatants were added and after homogenization, 20 mL were transferred and put in a boiling bath (for 4 min). Then, the tubes were removed and min), and once cold, the samples were centrifuged (15,000 g, 20 min, 4 °C) were then filtered (nylon 0.45 mm) and stored until injection. The samples in an HPLC (Waters, Milford, USA), coupled to a refractometric detector equipped with a SugarPak 1 column (Waters 6.5 × 300 mm) and pre-column

Sugar Content in Fruits
Sugar extraction followed the procedure of Medlicott and Thompson (1985) [30]. A total of fifteen pears per treatment (n = 3, thus 5 fruits per sample) were firstly cleaned with deionized water and then peeled, followed by a longitudinal cut. A total of 40 g of pulp (8 g per fruit) per sample was added to 150 mL of cold ultrapure water and liquified, followed by the addition of ultrapure water until 200 mL. Samples were kept in ice, then were transferred to ultrasounds (for 5 min) and were later centrifuged (15,000× g, 15 min, 4 • C). The supernatant was transferred to glass tubes in ice, while the pellet was resuspended in ultrapure water following a new centrifuge in the same conditions. The supernatants were added and after homogenization, 20 mL were transferred to glass tubes and put in a boiling bath (for 4 min). Then, the tubes were removed and put into ice (6 min), and once cold, the samples were centrifuged (15,000× g, 20 min, 4 • C). The samples were then filtered (nylon 0.45 mm) and stored until injection. The samples were injected in an HPLC (Waters, Milford, DE, USA), coupled to a refractometric detector (Waters 2414), equipped with a SugarPak 1 column (Waters 6.5 × 300 mm) and pre-column (Wat 088141) with SugarPak II inserts (Wat 015209). Ultrapure water containing 50 ppm calcium EDTA was used as the mobile phase, with a flow of 0.5 mL min −1 , and an injection volume of 40 µL for each sample. The data were later analyzed with the software Breeze and a quantification was performed based on the calibration curves of sucrose, glucose, fructose and sorbitol.

Lipid Content in Fruits
A total of twenty pears per treatment (n = 4, thus 5 fruits per sample) were selected and cleaned with deionized water and then peeled. A total of 5 g of pulp (1 g per fruit) per sample were weighted. Fatty acid composition was determined according to Vidigal et al. (2018) [31]. To each sample, 10 mL of a solution of methanol: sulfuric acid (CH 3 OH:H 2 SO 4 , 39:1, v:v) were added, followed by the addition of an internal standard (C17:0, heptadecanoic acid). The tubes (with a teflon stopper and septum) were then transferred to a 70 • C bath (for 60 min). Once cooled, 10 mL of petroleum ether and 6.7 mL of ultrapure water were added. After homogenization with vortex, they were left to decant (for 60 min), followed by the removal of the top phase to tubes with a teflon cap. The tubes were put to dry in a 40 • C bath and under a stream of nitrogen, being then resuspended in GC-grade n-Hexane, and then the sample was stored in a vial with a teflon septum at −80 • C until injection.
Esterified fatty acids were analyzed on a gas-liquid chromatograph (CP-3380, Varian, Palo Alto, Santa Clara, CA, USA), coupled to a flame ionization detector (GC-FID) and separated by means of a Varian capillary column (CP-Wax 52 CB). Total fatty acids (TFA) and the relative abundance of fatty acids (in %) were attained. The degree of unsaturation was obtained through the unsaturation index (DBI-double bond index), which reflects the relative abundance of mono-and polyunsaturated fatty acids in relation to saturated fatty acids, obtained by using the formula: DBI = [(X% monoenes + 2 X% dienes + 3 X% trienes)/% saturated fatty acids], according to Mazliak (1983) [32].

Statistic
Statistical analysis was carried out using a Two-Way ANOVA (p ≤ 0.05) to assess the differences; then, a Tukey's for mean comparison was performed, considering a 95% confidence level. Letters a, b and c represent significant differences among treatments for each date or between regions, while A and B represent significant differences between the analytical dates for each treatment.

Mineral Quantification and Location in Rocha Pear Fruits
At harvest, the five zones of the equatorial region of all treatments of Rocha pear fruits revealed ( Figure 2) higher Ca contents than the control. Calcium showed a heterogeneous distribution in fruit tissues, prevailing in the center (zone 1) and near the epidermis (zone 5). Relative to all the analyzed minerals, the content of K prevailed. However, for most treatments (except T0.6), zones 1 and 3 displayed levels of K inferior to the control ( After 5 months of storage, relative to the control, all the sprayed fruits displayed higher values for Ca (Table 1) in all five zones. However, Ca heterogeneous distribution in fruit tissues persisted, with higher values prevailing in the core (e.g., center) and near the epidermis (zone 1 and 5, respectively). Relative to the other minerals, K maintained the highest content. Nevertheless, like at harvest, for most treatments (except T0.6), zones 1 and 2 showed (Table 1) lower values than the control, whereas higher values occurred in zones 3, 4 and 5 (except zone 5 for treatment T0.1). Relative to the control, Mn in the sprayed fruits revealed inferior values only in zone 1, remaining higher in four regions as at harvest (Figure 2). The zinc values (Table 1) in the sprayed fruits were only inferior in zones 1 and 2 (except for treatment T0.8). Similarly for Fe (Table 1), the same two zones per treatment were inferior to the control (except for treatment T0.8 and zone 5 for T0.6). Copper values (Table 1) remained lower in zones 1 and 2 and for T0.1 also in zone 5. After 5 months of storage, relative to the control, all the sprayed fruits displayed higher values for Ca (Table 1) in all five zones. However, Ca heterogeneous distribution in fruit tissues persisted, with higher values prevailing in the core (e.g., center) and near the epidermis (zone 1 and 5, respectively). Relative to the other minerals, K maintained the highest content. Nevertheless, like at harvest, for most treatments (except T0.6), zones 1 and 2 showed (Table 1) lower values than the control, whereas higher values occurred in zones 3, 4 and 5 (except zone 5 for treatment T0.1). Relative to the control, Mn in the sprayed fruits revealed inferior values only in zone 1, remaining higher in four regions as at harvest (Figure 2). The zinc values (Table 1) in the sprayed fruits were only inferior in zones 1 and 2 (except for treatment T0.8). Similarly for Fe (Table 1), the same two zones per treatment were inferior to the control (except for treatment T0.8 and zone 5 for T0.6). Copper values (Table 1) remained lower in zones 1 and 2 and for T0.1 also in zone 5. Following a general perspective, in stored Rocha pears, Ca at different extends triggered a heterogeneous distribution of minerals (Table 1). Calcium increases in the interior part of the fruits occurred (zone 1 to 4, except zone 4 for treatment T0.8), whereas K prevailed in the middle region of the pulp (zones 3 and 4), and for the remaining mineral elements content (Mn, Fe, Zn and Cu), slight decreases in the treatments with sprays of Ca(NO 3 ) 2 occurred.

Sugar and Lipid Content
At harvest, no significant differences occurred among the Rocha pear treatments, but the contents of fructose prevailed in all the treatments ( Table 2). After 5 months of storage, relative to the control, sucrose revealed significantly higher values in T0.1 and T0.6, whereas in glucose and fructose this occurred in T0.1 ( Table 2). Relative to the control, sorbitol and total sugar levels ( Table 2) also displayed higher values in T0.1 and T1.6.
At harvest, TFA did not reveal significant variations among treatments (Table 3). For fatty acids <16:0, treatment T0.8 was significantly higher than the control, while C16:0 showed significantly lower values in T0.1 in regard to T0.8 (Table 3). In this context, when compared with the control, C18:0 and C18:2 did not reveal any significant deviations, but C18:1 significantly decreased with the application of CaCl 2 , whereas C18:3 increased  (Table 3). Relative to the control, the DBI of the sprayed fruits did not vary significantly. Table 2. Average ± S.E. of sugar content (sucrose, glucose, fructose, sorbitol and total) from Rocha pear from September (harvest) and March (5 months of storage). Treatments Ctr, T0.1, T0.6, T0.8 and T1.6 correspond to the control and initial foliar spraying with 0.1 and 0.6 kg·ha −1 Ca(NO 3 ) 2 and 0.8 and 1.6 kg·ha −1 CaCl 2 , respectively. Letters a, b and c represent significant differences among treatments for each date, while A and B represent significant differences between harvest and 5 month storage for each treatment. After 5 months of storage, significant differences could not be found among treatments for TFA, fatty acids <16:0, C16:0, C18:0, C18:1 and the DBI but, relative to the control, C18:2 and C18:3 showed significantly higher and lower values for T1.6, respectively (Table 3).
Relative to the harvest period, after 5 months of storage, TFA and C18:1 decreased significantly in all treatments, but significantly higher values (3.21-fold) were found for T0.1 of fatty acids <16:0 (Table 3). All treatments of C16:0 significantly augmented after 5 months of storage, but the opposite occurred with C18:0 (except T1.6) ( Table 3). At harvest, and relative to 5 months of storage, C18:2 revealed significantly lower values in T1.6 (decreased 19.8%), whereas in C18:3 a similar trend was found with Ctr, T0.1 and T0.6 (decreased 72%, 64.4% and 75.2%, respectively). After 5 months of storage, significantly lower DBI values were only found for T0.1. Table 3. Average ± S.E. of total fatty acid content (TFA), fatty acids profiles (relative abundance, mol %) and double bound index (DBI) of lipids from Rocha pear fruits at harvest and after 5 months of storage. Treatments Ctr, T0.1, T0.6, T0.8 and T1.6 correspond to the control and foliar spraying with 0.1 and 0.6 kg·ha −1 Ca(NO 3 ) 2 and 0.8 and 1.6 kg·ha −1 CaCl 2 , respectively. Letters a, b and c represent significant differences among treatments for each date, while A and B represent significant differences between harvest and 5 months of storage for each treatment.

Discussion
As previously found in different pear varieties [16][17][18][19][20]33] and apples [34,35], preharvest foliar spraying with Ca (with either Ca(NO 3 ) 2 or CaCl 2 ) increased this mineral content in Rocha pear fruits at harvest (Figure 2). Calcium can be applied in the soil or via foliar spraying (excluding soil as "intermediate"), but its solubility (varying with the chosen chemical compound) also affects the availability for plant absorption [36]. In fact, CaCl 2 (commonly applied by foliar sprays) and Ca(NO 3 ) 2 (commonly applied on soil or through fertirrigation) are soluble compounds that become rapidly available in comparison to other sources such as calcium carbonate (CaCO 3 ) or calcium sulfate (CaSO 4 ) [36]. Nevertheless, Ca accumulation in fruits can vary with phase and frequency of fertilizer application during production, edaphoclimatic conditions or genotype [37]. For instance, for apples, up to 90% of Ca assimilation can occur in the first 4 to 6 weeks after bloom [36], whereas for Rocha pears this period can range from budbreak up to 30 to 40 days after bloom [38]. However, the use of lower concentrations (0.5-2.0%) is advised in the initial stages of the production cycle to avoid damaging plant structures such as leaves, while higher concentrations can be applied later since the effects on trees or fruits is low [37,38]. In this context, Ca(NO 3 ) 2 has a more pronounced effect on fruits, while CaCl 2 mainly affects leaves [39]. Indeed, after spraying Conference pears with CaCl 2 (between 10 kg·ha −1 -25 kg·ha −1 ), damages could not be found [18]. Concerning the contents of nutrients in Rocha pears, depending on the edaphoclimatic conditions and fertilization workflows, some heterogeneity has been reported. For instance, according to PortFIR (2022) [24,40], K content prevails in larger quantities (150 mg/100 g FW , 960 mg/100 g DW ), followed by Ca (9 mg/100 g FW , 57 mg/100 g DW ), Fe (0.3 mg/100 g FW , 1.9 mg/100 g DW ) and Zn (0.2 mg/100 g FW , 1.3 mg/100 g DW ). In another study by Mendes (2017) [41] about the content in healthy Rocha pear fruits from five orchards, after storage from 3 to 6 months, the contents (on a dry weight basis) for K, Ca  (Table 1), our data also revealed that mineral ranges followed macronutrients and micronutrients classification [43]. Furthermore, Saquet et al. (2019) [42] also found that in Rocha pears prevails a radial decrease in Ca, Fe, Mn, Zn and Cu contents from the fruit skin to inner flesh tissues (but K values followed an opposite trend) and Raese and Drake (2000) [33] studying the application of CaCl 2 in a different variety also detected a similar trend for Ca accumulation between the cortex and the peel (471-524 ppm and 1563-1729). A putative explanation for the heterogeneous distribution of Ca among the tissues of the Rocha pears fruits (Figure 2; Table 1) might implicate its absorption after spraying as well as the progressive inhibition of mineral influx to the fruits in the later stages of development, due to xylemic vessel degradation [37,44]. Accordingly, in the initial phases of fruits development, Ca accumulation implicates its absorption at the epidermis but also its accumulation through xylem flux in the core. Moreover, after a progressive degradation of the xylem vessels, Ca diffusion from the epidermis to the core of the fruit was responsible for different accumulation patterns within Rocha pear tissues until harvest and during storage ( Figure 2; Table 1). Mineral enrichment in plant species determines synergistic or antagonistic interactions among mineral accumulation [45]. Nevertheless, at harvest and in most of the treatments, the general increase in K, Fe, Mn, Zn and Cu in Rocha pears clearly points a synergism with Ca accumulation (Figure 2). Moreover, in plant species, antagonistic interactions between Ca and K, due to the similar chemical characteristics, often leading to competition for uptake or transport, have been reported [45]. Additionally, the capacity of large amounts of Ca to modify the permeability of cell membranes has been link to the inhibitory effect on K contents [45]. However, in the tissues of Rocha pear fruits, an opposite trend was found since K mobilization and accumulation occurred preferable outside the core zones from harvest and during storage (Table 1). This tendency was also found in apples [35,46,47] and tubers [48] after spraying with CaCl 2 and with Ca(NO 3 ) 2 , and in pears [17] with CaCl 2 . Although Fe, Mn and Cu have a low mobility in plant tissues, while Zn keeps an intermediate translocation [43,[48][49][50][51], the increasing contents of Ca in pear Rocha fruits did not have a negative impact on micronutrients accumulation (Figure 2), and still with storage their concentrations prevailed outside the core zones (Table 1). Nevertheless, the interactions between Ca and Zn, Mn, Fe and Cu seem to depend on plant genotypes and growth conditions. In fact, a study by   [52] showed that Zn and Mn either maintained or significantly decreased in two apple varieties sprayed with Ca(NO 3 ) 2 and CaCl 2 , while Fe and Cu increased for the variety 'Golden Delicious' but decreased for 'Jonagold'. Concerning grapes, synergistic and antagonistic interactions were also found between Zn and Ca accumulations in the varieties 'Castelão' and 'Moscatel', respectively [50]. Additionally, in two varieties of tubers, the increasing accumulation of Ca triggered by Ca(NO 3 ) 2 and CaCl 2 foliar spraying presented different accumulation trends of Fe and Zn [48].
Sugars are a product of photosynthesis, accounting as a source of energy for plants [53] and further contributing to fruits' flavor (namely sweetness), color, texture and nutritional values [54,55]. According to PortFir (2022), ANP (2022) and   [24,27,55], among the different varieties of pear fruits, the amount of total sugars usually varies between 6.50 g/100 g FW and 13.20 g/100 g FW , with this amount only surpassed by water content. However, at harvest, the control and treated Rocha pears in some cases displayed higher values (Table 2), which can be attributed namely to the specificity of the genotype characteristics (as found from a total of 22 varieties of pears [56]) and edaphoclimatic conditions [15]. Additionally, still at harvest, the absence of significant differences in each sugar among treatments (Table 2) indicated that foliar applications with Ca did not have a negative impact on sugar content. After 5 months of storage, relative to the control, the average content of all sugars from the different Ca treatments showed higher values ( Table 2). The sugar content of fruits changes during the maturation, ripening and senescence phases, due to the hydrolysis of complex polysaccharides (such as starch synthesized in the early stages of fruit development) into simpler sugars (such as glucose), thus increasing fruit sweetness [57]. These changes keep occurring during pear storage since they are climacteric fruits, and thus maintain metabolic activities such as respiration [28]. The main photoassimilate produced by photosynthesis and transported to apples or pears is sorbitol (i.e., the translocation of 60-85% of the carbon, the rest being sucrose [44]). Nevertheless, as found in our study (Table 2), polyols such as sorbitol can only account for 0.003-6.8 g/100 g FW [55] because its conversion into other sugars (such as glucose, fructose, sucrose and starch) occurs during the ripening stage when it reaches the fruit [44]. Additionally, in fruits, sucrose is either transported from other plant tissues or is synthetized from the existent sorbitol [58], whereas its decrease with storage relates to hydrolysis reactions into its monomers [55].

Conclusions
Trees of Rocha pears sprayed with Ca(NO 3 ) 2 and CaCl 2 increase Ca content in the center and near the epidermis of the fruits and further affects the levels of all the studied minerals in tissues. The heterogeneous distribution of Ca for both moments of analysis results from its absorption in the peel of the fruit after Ca(NO 3 ) 2 and CaCl 2 spraying and from the xylem flux in the core prior to maturity. The differential Ca accumulation among tissues of Rocha pears does not affect the permeability of cell membranes and therefore K and micronutrients accumulation were not inhibited. Additionally, at harvest, Ca does not affect the levels of the four analyzed sugars, and after storage, their concentration remains higher in Ca-treated fruits. At harvest and independent of Ca treatments, the relative proportions of FA in Rocha pears remained, but after storage the treatments with Ca displayed a different trend. In this context, storage decreases the amount of TFA; however, the DBI indicates that cell membrane fluidity remains unaffected.