Structures related to resprouting potential of two Myrtaceae species from Cerrado: morpho-anatomical and chemical studies

Resprouting is a functional trait in species which occur in fi re-prone ecosystems. These plants can resprout from aerial buds and by recruiting belowground bud bank using carbohydrates allocated in roots as resource. In this study, we present morpho-anatomical features and chemical composition related to the resprouting potential of two species of Eugenia L. in an area of the Cerrado (Brazilian savanna) under regeneration, after the clear-cutting of Pinus sp. with the later burning of pine needles layer. We used standard histological techniques for belowground organs analysis and aerial buds protection degree. Belowground buds in layer from soil surface down to 10 depth were counted and the chemical analyses were performed on roots. In all aerial buds, there were relevant protection traits. The belowground organ is a sobole and the number of buds in its upper portion varied from 24 to 517 between individuals of both species. Phenolic compounds, fl avonoids, starch and other carbohydrates were detected in roots. The protection of aerial buds, the large number of belowground buds and the storing and protective compounds may have favored the resprouting of the species in


INTRODUCTION
The ability of resprouting in response to environmental disturbances is currently recognized as a key functional trait among woody species and as basis of resilience of these plants in the environment. This ability is determined by the development, protection degree and viability of a bud bank (Clarke et al. 2013), which refers to buds in both aerial and belowground systems (Klimešová & Klimeš 2007). The knowledge of location and protection degree of these buds is important to better understanding of the regeneration mechanisms (Vesk & Westoby 2004). In fi re-prone ecosystems, like the Brazilian Cerrado, fire events occur frequently, and vegetation is modifi ed as a consequence of the damage or loss of plants aboveground biomass (Clarke et al. 2013, Pereira-Júnior et al. 2014. Resprouting from aerial buds has advantage over resprouting from buds allocated in belowground organs (Burrows & Chisnall 2016) for providing a rapid growth in height. However, especially in woody plants, aerial buds require greater protection (Charles-Dominique et al. 2015), which can be conferred, for example, by a thick bark (Burrows & Chisnall 2016), even though this is not an autonomous attribute (Charles-Dominique et al. 2015). In general, these buds have any of these protection traits: scales, stipules, base of corresponding leaf (Bell et al. 1999), epidermal appendices, such as trichomes (Burrows 2008) and colleters (Silva et al. 2012), as well as the presence of stone cells, phenolic compounds, crystals, lipids and thick cuticle (Bell et al. 1999) and can regenerate their aerial shoots after disturbances from axillary and accessory buds (Burrows 2008).
Plants responses to that disturbance are yielded by traits developed along evolutionary history (Simon et al. 2009), for example, the recruitment of a belowground bud bank (Klimešová & Klimeš 2007), that promote persistence and aboveground biomass regeneration, restoring vegetation (Rodrigues et al. 2004, De Moraes et al. 2016, Paula et al. 2016). This bud bank can be allocated in different belowground organs, which are protected by soil, an excellent thermal insulator (Clarke et al. 2013, Pausas et al. 2018). Lignotubers, more common in ecosystems where fires of highintensity are frequent (Paula et al. 2016), exhibit a large number of buds with high protection degree as observed in Western Australian Oil Mallee (Wildy & Pate 2002).
For resprouting after disturbance not only bud bank is necessary but also storage of carbohydrates. When the photosynthetically active tissue are absent, the storage compounds, such as glucose, fructose, sucrose, maltose, raffinose, inulin and levan type fructans, maltooligosaccharides and, more frequently, starch, are the main carbohydrates in Cerrado species, which are mobilized for resprouting after disturbance (Bombo et al. 2014, De Moraes et al. 2016, Filartiga et al. 2017a, Pausas et al. 2018). In addition to supplying energy for resprouting, some carbohydrates may offer an alternative mechanism for osmoregulation, protecting plants against low temperatures (Asega et al. 2011) and hydric deficit (Dias-Tagliacozzo et al. 2004, De Moraes et al. 2016.
Individuals from several botanical families worldwide have the ability to regenerate their photosynthetic shoots in fire-prone ecosystems (Burrows 2008

Study site and sampling
The study was conducted in a Cerrado region under regeneration, at the ecological station of Santa Bárbara, at Águas de Santa Bárbara municipality, São Paulo State, Brazil (22º48'59"S; 49º14'12"W). In 2012, Pinus sp. trees were removed after cultivation since the 1970s and the layer of pine needles was burned in 2014. Species of Eugenia dysenterica (Mart.) DC. and E. punicifolia (Kunth) DC. (Myrtaceae) were selected due the large number of resprouted individuals in the area after the fire event (Pilon and Durigan, personal communication). These species are perennial, native and endemic of Brazil. The habit varies between shrub and tree in E. dysenterica and, shrub and subshrub in E. punicifolia (Sobral et al. 2015). Both species occurs in Caatinga, Central Brazilian Savanna and Atlantic Rainforest phytogeographic domains (Sobral et al. 2015). The material was identified and deposited at the herbarium ESA under the numbers 140288, 140289, 140286 and 140287.

Bud protection
Three branches with apical buds and three subsequent nodal regions of three individuals of each species were fixed in FAA 50 (1:1:18; formaldehyde, glacial acetic acid and 50% ethanol) (Johansen 1940) for 48 h, dehydrated in a graded ethanol series and included in plastic resin Leica ® . Longitudinal sections were obtained using a Leica 2025 rotary microtome with disposable steel knives at 7 µm. The sections were stained with 0.05% toluidine blue in phosphate-citrate buffer, pH 4.5 (Sakai 1973) and mounted in Entellan ® synthetic resin (Merck ® ) for histological analysis. Other sections were subjected to the test with Sudan IV for total lipids (Jensen 1962), and ferric chloride for phenolic compounds (Johansen 1940). To detect cellulose, we used Calcofluor White M2R fluorochrome (Hughes & McCully 1975) and analysis in an epifluorescence microscope using filter A (Excitation 325-375 nm, Emission 435-485 nm).

Colleters
Five branches with apical bud and three subsequent nodal regions were collected from three individuals of each species. For the histological analyses, samples were fixed in Karnovsky solution (Karnovsky 1965) for 48 h and processed as described on previous topic. Part of the cross-sectional and longitudinal sections were stained with 0.05% toluidine blue in phosphate buffer and citrate pH 4.5 (Sakai 1973) and mounted in Entellan ® synthetic resin (Merck ® ). Other sections were subjected to tests with Aniline blue black to identify the presence of protein compounds (Fisher 1968), ruthenium red for acidic mucilage (Gregory & Baas 1989), PAS reagent for total polysaccharides (Periodic Acid-Schiff) (McManus 1948) and ferric chloride for phenolic compounds (Johansen 1940). Fresh samples were also submitted to ruthenium red reagent. For Scanning Electron Microscope (SEM), samples were fixed in Karnovsky solution (Karnovsky 1965), dehydrated in a graded ethanol series, critical-point dried using CO 2 (Horridge & Tamm 1969), mounted on aluminum stubs and coated with a thin layer (30-40 nm) of gold. The observations and eletromicrographs were made by SEM model LEO VP 435 (Zeiss,Oberkochen,Germany), operated at 20 kV, with scales directly printed.

Belowground system
Cross and longitudinal sections of different regions of the belowground organs of three individuals of both species, still fresh, were made using a sliding microtome (Leica SM2000 R) with disposable steel knives to identify the anatomical structure and carry out the following histochemical tests: Sudan IV (Jensen 1962) and Sudan Black B (Pearse 1968) for total lipids; ruthenium red for acidic mucilage (Gregory & Baas 1989); zinc chloride iodine for starch grains (Strasburger 1913) and ferric chloride for phenolic compounds (Johansen 1940). Some root samples were fixed in formalin-ferrous sulphate for detection of phenolic compounds (Johansen 1940). Samples of different regions of belowground systems with buds were fixed in FAA 50 (Johansen 1940) for 48 h and processed as described in topic 1. The sections were stained with 0.25% safranin (Gerlach 1984, modified) and 1% alcian blue (Luque et al. 1996) and mounted in Entellan ® synthetic resin (Merck ® ).
For all items above, control sections were carried out as the standard procedure to confirm the histochemical tests. Digital photomicrographs were obtained using a Leica DMLB microscope and Leica DFC310 Fx camera. LAS 4.0 software (Leica) was used for image analysis. Some images were obtained with polarized light.

Belowground bud bank
The belowground bud bank was evaluated in layer from soil surface down to 10 cm depth where most buds are found in belowground systems in the Cerrado (Appezzato-da-Glória 2015 and literature cited). Evaluation and count was performed in belowground systems of three individuals of each species using an Opton Trinocular Stereoscopic Microscope. Digital images were obtained using a Leica DFC295 camera coupled to a Leica M205 C Stereoscopic Microscope. After counting, samples with buds were separated for the anatomical studies described above.

Chemical analyses of roots
Root samples from three individuals of each species were sectioned with a microtome and milled. The samples were dissolved in ultrapure water and vacuum-filtered in cellulose nitrate Millipore membrane with 0.45 μm pore diameter. The filtrate was treated with an aluminum-based bleaching mixture to reduce influence of pigments in total carbohydrate quantification. Total carbohydrate contents were analyzed by the phenol-sulphuric method (Dubois et al. 1956). The curve was made with glucose as standard and the results expressed as g of carbohydrate per 100 g of roots.
Then 5 g of the milled samples were extracted in ethanol using Sohxlet apparatus (Ferraz et al. 2000). Total phenolics and flavonoids were quantified from the ethanolic extracts.
The total phenolics were determined by mixing 100 µL of the ethanolic extract of samples with 900 µL of ultrapure water. Then, we added 0.5 mL of Folin-Ciocalteu reagent diluted at 1:10 (v/v) in ultrapure water. After 40 min, 2.5 mL of 4% Na 2 CO 3 (m/v) was added and the readings were made in UV-visible spectrophotometer at 725 nm. The results were expressed as micrograms of tannic acid equivalent (TAE) per 100 g of roots.
Total flavonoids were determined using a solution with 0.5 mL of ethanolic extract, 4.3 mL of 80% ethanol (v/v), 0.1 mL of 10% Al (NO 3 ) 3 (m/v) and 0.1 mL potassium acetate (1 mol L -1 ). After 40 min at rest at room temperature, absorbance was read in UV-visible spectrophotometer at 415 nm (Park et al., 1995). The results were expressed as micrograms of rutin equivalent by 100 grams of roots.
All analyses were carried out in triplicate and the results were submitted to the t test (p < 0.05 and p < 0.01) through the statistical package Assistat.

Bud Protection
In both E. dysenterica and E. punicifolia, besides the apical bud of the branches (Figs. 1a, b) in the three subsequent nodal regions above the axillary bud (Figs. 1c,d), an accessory bud occurs (Figs. 1e,f,arrows). In all the aerial buds, colleters occur (Figs. 1a,d,arrows). For description see next topic. The shoot apical meristem (SAM) is protected by leaf primordia with many unicellular non-glandular trichomes that also occur in young stem extension around the buds (Figs. 1a-k). These trichomes are whitish and have parietal thickening in cellulose (Fig. 1b, inset) and phenolic compounds may accumulate . In the well-developed leaf primordia, the epidermal cells are covered by a thickened cuticle (Fig. 1g). Phenol accumulation was also observed in other epidermal and subepidermal cells, mainly, those faced to the abaxial surface of leaf primordia (Fig. 1h). There are oil cavities in the subepidermal cells (Fig. 1f). In the mesophyll, there are crystal idioblasts (Fig. 1g) and others that accumulate phenolics (Fig. 1h). The crystals also occur in buds below the SAM (Fig. 1g).

Colleters
In both species, colleters are already present in shoot apices occupying the lateral side and intrapetiolar position (Figs. 2a-e). The number and size vary; however, the shape is constant. There is only one colleter inserted on the lateral sides of the leaf primordia at the nodal region (Figs. 2a,b). Generally, there are six colleters in intrapetiolar position (Figs. 2c,d). Sizes range from 407 to 780 µm and the circular diameter (Figs. 2e, f) is smaller at the apex than at the base (Fig. 2d). Some colleters are short-pedunculate, where non-secretory cells occur at the base (Fig.  2g) and other are sessile.
In both Eugenia analyzed species, the colleters are emergences that originate on the adaxial face of leaf primordia from divisions of protoderm and ground meristem cells (Figs. 2e, f). There is no participation of the procambium; therefore, the colleters are not vascularized. In secretory phase, the colleters are translucent (Fig. 2d) and constitute an elongated axis of parenchyma cells coated by epidermis of non-palisade cells (Fig. 2g) covered by a thin cuticle.
The sticky secretion (Figs. 2h, i) reacts positively to PAS reagent (Figs. 2j, k) and ruthenium red (Figs. 2l-n) confirming its mucilaginous nature. The reaction with Aniline blue black was negative. The secretion accumulates in the cytosol and in the large intercellular spaces of parenchyma (Figs. 2j, k, arrows). The secretion is eliminated between epidermis cells (Fig. 2k, arrowheads) at the apex (Fig. 2l), along the axis (Fig. 2m, arrow) and at the base (Fig. 2n), where it accumulates on the axillary bud (Figs. 2c-m, arrow). The senescence starts at the colleter apex with the collapse of cells (Fig. 2j, inset), which begin to accumulate phenolic compounds after secretion (datum not shown). In some samples, there was the presence of bacteria associated with the secretion released by these structures (Fig. 2i).

Belowground Bud Bank
The number of buds in the first 10 cm beneath soil level varied between individuals of the same species for both E. dysenterica (Fig. 3a) (162, 253, 517) and E. punicifolia (Fig. 3e) (24, 40, 109). The variation was due to the number of branches of the belowground structures. These branches are stems; therefore, buds were axillary (Fig. 3d). The buds were located preferentially in the first 5 cm and, in some cases, were displayed only after removing the protective scales (Fig. 3b, c) or the covering tissue (Fig. 3f).

Belowground systems anatomy
The belowground system of E. dysenterica is composed of a woody axis whose upper portion is a stem which emits aerial branches, while the lower portion consists of a thickened axial root that can reach up to 1 m deep (Figs. 4ad). The size of the belowground stem portion varies between individuals and can produce  dysenterica (a, c, d, e, f, i, j, k, m) and E. punicifolia (b, g, h, l, n). Scanning electron micrographs (a-c, h, i), stereomicroscope photographs (d, l-n), cross (e, f, j, k) and longitudinal (g) sections of the shoot apex.  adventitious roots with slender and tuberized portions (Figs. 4a, iii and iv). The periderm that covers all the belowground axis consists of layers of suberized cells (Fig. 4e) containing phenolic compounds alternated with layers of cells whose inner periclinal walls are pectin thickened (Fig. 4f). Groups of fibriform sclereids are observed in the vascular cylinder, in the axial system of secondary phloem (Fig. 4g, arrows) and the parenchyma cells accumulate starch and phenolic compounds. The radial parenchyma cells are dilated in the outer portions of vascular rays and these cells accumulate phenolic compounds and starch (Fig. 4g). Phloem cells have a natural orange coloring content of phenolic nature. In the belowground axis non-tuberized portions, the secondary xylem presents a smaller number  (Figs. 4j,  k). Therefore, starch accumulation is greater in tuberized portions (Fig. 4k). The caulinar axis has internal secondary phloem (Fig. 4c, h), with accumulation of phenolic compounds in the radial parenchyma and a prominent medulla composed of parenchyma cells containing phenolic compounds and scarce starch grains. In root portions, the exarch primary xylem occupies the center of the organ (Fig. 4d).
In E. punicifolia, the belowground stem forms horizontal portions by which aerial branches and adventitious roots are emitted. The taproot and the adventitious roots occupy a surface region of soil and, as well as the stem, they are distributed in a more horizontal plane (Fig. 5a). The periderm of the stem axis of E. punicifolia differs from the roots, since this tissue exhibits layers of cells with thickened lignified walls alternated with layers of cells with suberized walls (Figs. 5b, c). In the vascular cylinder of stem, the secondary phloem is well developed with dilated phloematic rays, whose dilatation results in a periclinal cell elongation and anticlinal divisions (Fig. 5d, e). There are calcium oxalate crystals and sclereids in the secondary phloem (Fig. 5f). Several cells of phloematic parenchyma contain natural orange coloring substance and others brownish hue (Fig. 5g), both react positively with ferric chloride and feature starch grains (Fig. 5h). Also in xylematic rays, in the internal phloem and medullary parenchyma, cells with orange content occur (Fig. 5i), which reacts positively to phenolic compounds (Fig. 5j), but starch grains are only observed in medullary cells.
In roots, regardless of the thickening degree, the periderm is similar to that described for the belowground stem and roots of E. dysenterica, with alternating layers of cells with suberized walls and cells with pectin-thickened walls (Fig.  5k, l). In the vascular cylinder, secondary phloem parenchyma also features cells containing starch grains, some of which have natural orange content (Fig. 5m) of phenolic nature (Fig.  5n) as observed in E. dysenterica. Similar to the belowground stem, phloematic rays present anticlinal divisions and tangential expansion of cells whose intensity depends on the thickening degree of roots (Fig. 5o). There are calcium oxalate crystals and sclereids in phloematic parenchyma (Fig. 5p). In secondary xylem, the vascular rays accumulate phenolic compounds (Fig. 5n) and starch grains. Inside the primary exarch xylem, cells can be lignified (Fig. 5q) or not (Fig. 5r).

Root chemical composition analysis
Total of free carbohydrates contents in roots of E. dysenterica and E. punicifolia were 4.17 g 100 g -1 of roots and 4.46 g 100 g -1 of roots, respectively. The content, without significant difference by the Tukey test (1% probability), refers to the concentration of carbohydrates solubilized in aqueous medium after maceration, and the insoluble material (fibers) was not analyzed. The species presented significant differences by the Tukey test (1% probability) with respect to concentrations of total phenolics compounds, being 2.54 mg per 100 g of root (TAE) for E. dysenterica and 13.66 mg per 100 g of root (TAE) for E. punicifolia. The concentrations of total flavonoids also presented significant differences by the Tukey test (1% probability) between species, being 1.18 mg per 100 g of root for E. dysenterica and 7.28 for 100 g of root for E. punicifolia. Analytical quantification of chemical components highlights their presence in the individuals studied.

Colleters
The exudate of colleters of the analyzed species reacts positively to detection of polysaccharides, commonly found in these structures (Silva et al. 2017, Ribeiro et al. 2017, which confirms its mucilaginous nature, responsible for its main function, which is to protect the meristem (Ribeiro et al. 2017). In addition to meristem protection, the presence of secretion and location of the colleters highlight the importance of these structures for protection of buds against excessive sunlight and high transpiration levels, reducing water loss , proliferation of fungi (Ribeiro et al. 2017), as well as can be considered as an adaptive factor in Myrtoideae (Silva et al. 2012). Colleters found in this work are the conic type, following the classification proposed by Silva et al. (2012), due to its circular format in cross section with decreasing diameter from base to apex. This type of colleter was observed in 19 species of Myrtoideae near the shoot apical meristem at the stem apex and in leaf axils (Silva et al. 2012). However, this is the first record of colleters in E. dysenterica and E. punicifolia, which are emergences originated from protoderm and ground meristem, a trait observed in species of Rubiaceae (Vitarelli & Santos 2009, Coelho et al. 2013 and Apocynaceae (Appezzato-da-Glória & Estelita 2000a). In the colleters of those families, the palisade epidermis is responsible for exudate secretion (Appezzato-da-Glória & Estelita 2000a, Martins et al. 2010b, Coelho et al. 2013. However, in the studied species and in the Myrtaceae species analyzed by Silva et al. (2012), epidermal cells are not elongated radially, but with a dense cytoplasm and positive reaction for total polysaccharides test. These characteristics are also observed in the parenchyma cells throughout the colleter axis, except on the peduncle when present. This homogeneous pattern of cells observed in colleters of Eugenia in this study and in Silva et al. (2012) has also been described in Fabaceae colleters (Paiva and Machado 2006, Coutinho et al. 2015, Silva et al. 2017).
In Eugenia dysenterica and E. punicifolia, the parenchyma has intercellular spaces typical of the ground tissue before the secretory phase; however, during the secretory phase, there is an increase of these spaces and exudate accumulation. This intercellular accumulation of secretion has been reported in other Myrtaceae species (Silva et al. 2012) and Hymenaea stigonocarpa -Fabaceae: Caesalpinioideae (Paiva & Machado 2006). These authors found pectic compounds in intercellular spaces and in the cytosol in all the parenchyma cells of colleter axis, as described in this paper. Colleters are not vascularized, as verified in other species (Martins et al. 2010b, Silva et al. 2017, Ribeiro et al. 2017. Secretion in colleters in E. dysenterica and E. punicifolia is released through spaces that form between the epidermal cells. This feature has been observed in species of Apocynaceae (Appezzato-da-Glória & Estelita 2000a, Martins et al. 2010b; however, in Myrtaceae, this is the first report of the secretion release process. Senescence of the analyzed colleters is initiated at the end of the secretory phase and characterized by brownish coloration at the colleter apex (Silva et al. 2012). The color change has been linked to oxidation of phenolic compounds as a product of senescence in apex cells (Coelho et al. 2013), followed by a collapse of these cells (L.A. Souza, unpublished data) as verified in E. dysenterica and E. punicifolia.

Belowground bud bank
The belowground systems of the analyzed species are soboles (woody rhizomes) whose upper portion emits horizontal stem branches that extend belowground level and form aerial projections and adventitious roots (Pausas et al. 2018). Among the 358 Myrtaceae species from worldwide fire-prone ecosystems listed by Pausas et al. (2018) in the supplementary database, all of them present lignotuber and only eight species have lignotuber and woody rhizome.
Studies on belowground bank buds with Cerrado species have shown a greater concentration of buds in the organ portion closer to ground level (Alonso & Machado 2007, Appezzato-da-Glória and Cury 2011, Bombo et al. 2014, Filartiga et al. 2017a, as observed in this work. Buds protection is an important trait in maintaining a viable bud bank, as these buds are protected by the soil (Vesk and Westoby 2004, Alonso & Machado 2007, Clarke et al. 2013). In addition, belowground buds in E. dysenterica and in other Cerrado species (Alonso & Machado 2007, Appezzato-da-Glória et al. 2008) are equipped with thick scales, which also confer protection to the shoot apical meristem.

Storage and protective compounds
Starch was found in large quantities in the studied Eugenia species. This carbohydrate provides direct energy to resprouting (Orthen 2001) and structural carbon necessary for the formation of new tissues during resprouting (De Moraes et al. 2016). In Eugenia dysenterica and E. punicifolia, as well as in thickened belowground organs of other species, reserve accumulation is usually related to the increase of number of cells in vascular parenchyma (Bell et al. 1996, Appezzato-da-Glória 2015, Abdalla et al. 2016. In E. dysenterica, starch accumulation is more prominent in the axial and radial parenchyma cells of secondary xylem, while in E. punicifolia accumulation occurs in cells of the phloematic parenchyma. In both species, there is no variation in cambium activity for the production of vascular parenchyma; however, there are anticlinal divisions and expansions of tangential walls of phloematic parenchyma cells that promote increase in organ thickness, mainly, in E. punicifolia. Soffiatti & Angyalossy-Alfonso (1999) also observed expansion of radial parenchyma cells forming a disordered array with the presence of crystals in Eugenia cerasiflora and E. uniflora and sclereids groups in E. uniflora. In Eugenia dysenterica and E. punicifolia, crystals and lignified sclereids groups are also observed in the secondary phloem. These structures are important for protection of belowground axis mainly against insect attack (Hudgins et al. 2003). In the belowground stem of both species and in Eugenia pyriformis (Armstrong et al. 2012), there is an inner phloem, which is a diagnostic feature in Myrtaceae (Metcalfe & Chalk 1950). On the root periderm of both species, there are alternating cell layers of suberized walls and cells with parietal thickenings in pectin. Given the hydrophilic pectin properties (Paiva et al. 2009), walls with pectic thickenings may be retaining moisture in the covering tissue. Furthermore, in the periderm of stem of E. punicifolia, there was the presence of cell layers with lignified walls, as reported in other Myrtaceae (Soffiatti & Angyalossy-Alfonso 1999, Armstrong et al., 2012 and in the terminal portion of soboles in Erythroxylum nanum (Alonso & Machado 2007).
In regard the reserve carbohydrates in studied Eugenia species, other compounds can be directly related to protection of belowground structures and, therefore, with the survival and resprouting potential of these plants. In the studied species, phenolic compounds were detected, not only on periderm, which is a frequent feature in belowground organs of Cerrado species (Appezzato-da-Glória & Cury 2011, Joaquim et al. 2014), but also in cells of the phloematic, xylematic and medullary parenchyma (when present). Some phenolic compounds and flavonoids may reduce digestibility for herbivores and act as phytoalexins, phytoanticipins and nematicides (Akhtar & Malik 2000, Kefeli et al. 2003, Howe & Schaller 2008, Bhattacharya et al. 2010). In addition, these compounds can polymerize and biosynthesize lignin, consequently strengthening cell walls (Kefeli et al. 2003, Bhattacharya et al. 2010. The difference in concentrations of phenolic compounds in E. dysenterica and E. punicifolia may indicate that roots of E. punicifolia have higher probability of antioxidant action and possible protection against attacks of nematodes and pests. In addition to phenolic compounds, flavonoids may also perform protection functions of belowground systems in the studied species, for example, by lignin polymerization for support and the antimicrobial action (Ferrer et al. 2008).
In conclusion, the high protection degree of buds in aerial organs, the presence and large number of buds in belowground structures, the accumulation of reserves and protection in belowground organs may have favored permanence of Eugenia dysenterica and E. punicifolia in the Cerrado region, as well as their resprouting after the clear-cutting of Pinus trees and burning of pine needles. In addition, the morphoanatomical and chemical characteristics presented are relevant to studies on the protection strategies and regeneration of plants subjected to environmental disturbances.