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Histochemical and ultrastructural study of Caesalpinia peltophoroides Benth. (Leguminosae-Caesalpinoideae) seeds

Estudo histoquímico e ultraestrutural de sementes de Caesalpinia peltophoroides Benth. (Leguminosae-Caesalpinoideae)

Abstracts

The objective of this work was to correlate data on light microscopy observations through histochemical analysis and polarized light techniques and investigations in transmission electron microscopy (TEM) to characterize the reserve materials in C. peltophoroides Benth. (Leguminosae-Caesalpinoideae) cotyledons, popularly known as "sibipiruna", a tropical tree species with wide distribution in Brazil. The cotyledon mesophyll, especially in the abaxial face, is rich in unsaturated neutral lipids contained in numerous lipid bodies dispersed in the cytoplasm. Proteins, more concentrated in the adaxial face of the cotyledons, occur in all the mesophyll and are stored in protein bodies containing globoids, with variable number and size, responsible for accumulation of mineral reserves. Calcium oxalate druses have distribution restricted to the cotyledons adaxial face and are associated with protein bodies. Starch, also distributed all over the cotyledon mesophyll, occurs in small amounts in plastids with developed lamellar system. Secretory cavities rich in phenolic compounds occur among procambial strands.

Histochemistry; compartmentalization; reserve materials


Este trabalho procurou correlacionar dados de observações em microscopia de luz através de técnicas histoquímicas e de luz polarizada e investigações em microscopia eletrônica de transmissão para caracterizar os materiais de reserva em cotilédones de C. peltophoroides Benth. (Leguminosae-Caesalpinoideae), conhecida popularmente como sibipiruna, ou falso pau-brasil, uma espécie tropical com ampla distribuição no Brasil. O mesofilo cotiledonar, especialmente na face abaxial, apresenta-se rico em lipídios neutros, insaturados, contidos em numerosos corpos lipídicos dispersos no citoplasma. As proteínas, mais concentradas na face adaxial dos cotilédones, ocorrem em todo o mesofilo e são armazenadas em corpos proteicos contendo globoides, com número e tamanho variáveis, responsáveis pelo acúmulo de reservas minerais. Drusas de oxalato de cálcio têm distribuição restrita à face adaxial dos cotilédones e estão associadas aos corpos proteicos. O amido, também distribuído por todo o mesofilo cotiledonar, ocorre em pequena quantidade em plastídios, com sistema lamelar desenvolvido. Entre os cordões procambiais ocorrem cavidades secretoras ricas em compostos fenólicos.

Histoquímica; compartimentalização; compostos de reserva


Histochemical and ultrastructural study of Caesalpinia peltophoroides Benth. (Leguminosae-Caesalpinoideae) seeds

Estudo histoquímico e ultraestrutural de sementes de Caesalpinia peltophoroides Benth. (Leguminosae-Caesalpinoideae)

Viviana Borges CorteI; Marília Contin VentrellaII; Eduardo Euclydes de Lima e BorgesIII; Claudia Aparecida PontesI; Daniel PinhoI

IPrograma de Pós-Graduação em Ciência Florestal da Universidade Federal de Viçosa (UFV), Viçosa-MG. E-mail:<viviborgescorte@yahoo.com.br> e <pontesac@gmail.com

IIDepartamento de Biologia da Universidade Federal de Viçosa (UFV), Viçosa-MG. E-mail: <ventrella@ufv.br>

IIIDepartamento de Engenharia Florestal da UFV. E-mail: <elborges@ufv.br>

ABSTRACT

The objective of this work was to correlate data on light microscopy observations through histochemical analysis and polarized light techniques and investigations in transmission electron microscopy (TEM) to characterize the reserve materials in C. peltophoroides Benth. (Leguminosae-Caesalpinoideae) cotyledons, popularly known as "sibipiruna", a tropical tree species with wide distribution in Brazil. The cotyledon mesophyll, especially in the abaxial face, is rich in unsaturated neutral lipids contained in numerous lipid bodies dispersed in the cytoplasm. Proteins, more concentrated in the adaxial face of the cotyledons, occur in all the mesophyll and are stored in protein bodies containing globoids, with variable number and size, responsible for accumulation of mineral reserves. Calcium oxalate druses have distribution restricted to the cotyledons adaxial face and are associated with protein bodies. Starch, also distributed all over the cotyledon mesophyll, occurs in small amounts in plastids with developed lamellar system. Secretory cavities rich in phenolic compounds occur among procambial strands.

Keywords: Histochemistry, compartmentalization and reserve materials.

RESUMO

Este trabalho procurou correlacionar dados de observações em microscopia de luz através de técnicas histoquímicas e de luz polarizada e investigações em microscopia eletrônica de transmissão para caracterizar os materiais de reserva em cotilédones de C. peltophoroides Benth. (Leguminosae-Caesalpinoideae), conhecida popularmente como sibipiruna, ou falso pau-brasil, uma espécie tropical com ampla distribuição no Brasil. O mesofilo cotiledonar, especialmente na face abaxial, apresenta-se rico em lipídios neutros, insaturados, contidos em numerosos corpos lipídicos dispersos no citoplasma. As proteínas, mais concentradas na face adaxial dos cotilédones, ocorrem em todo o mesofilo e são armazenadas em corpos proteicos contendo globoides, com número e tamanho variáveis, responsáveis pelo acúmulo de reservas minerais. Drusas de oxalato de cálcio têm distribuição restrita à face adaxial dos cotilédones e estão associadas aos corpos proteicos. O amido, também distribuído por todo o mesofilo cotiledonar, ocorre em pequena quantidade em plastídios, com sistema lamelar desenvolvido. Entre os cordões procambiais ocorrem cavidades secretoras ricas em compostos fenólicos.

Palavras-chave: Histoquímica, compartimentalização e compostos de reserva.

1. INTRODUCTION

Lipids, proteins, carbohydrates and mineral ions represent the main reserve material in seeds. They determine nutritional, industrial and technological characteristics and significantly contribute to ecophysiological characteristics, such as germination, initial seedling growth and species establishment (BUCKERIDGE et al. 2004). During germination and initial seedling growth, the reserve materials should work as an energy source (ATP) to maintain metabolic processes, and as source material for the synthesis of new molecules and tissues that will constitute the seedlings (BEWLEY and BLACK 1983). The content and chemical composition of reserve materials can vary markedly, but they are accumulated in specific organelles that may be present in embryonic or reserve tissues, such as the endosperm and perisperm (BEWLEY and BLACK 1983; BUCKERIDGE et al 2004).

The lipids are synthesized from membranous compartments of the cytoplasm, accumulated in lipid bodies where there is predominance of triacylglycerides that provide energy and structural membrane blocks during the initial germination stages and embryo growth (MURPHY 1990). Under the action of lipases, the fatty acids are liberated and catabolized to produce ATP and acetyl-coA, which is converted to sucrose by the glyoxylate pathway (MURPHY 1990; BUCKERIDGE et al. 2004). Starch, synthesized and accumulated in amyloplasts, is the main carbohydrate reserve in seeds, usually constituted by amylopectin and amylose (MORRISON 1992). During germination, starch is degraded by hydrolysis to maltose, which is later broken down into glucose that can be oxidized or transformed into sucrose. Other reserve carbohydrates can also be found, such as polysaccharides from cell wall, besides sucrose and carbohydrate from raffinose series (BUCKERIDGE et al 2004). Two protein classes are found in seeds, globulins and prolamins, synthesized from the endoplasmic reticulum and the Golgi complex, which are accumulated in protein bodies (MARTY 1999). Proteins serve as the main sulfur nitrogen source and, although not used as ATP sources, they supply carbon skeletons that serve as substratum for the synthesis of others compounds (BUCKERIDGE et al 2004).

Many structural and chemical works have sought to identify reserve compounds in seeds and their cellular compartmentalization (BAGLEY et al. 1963; HORNER and ARNOTT 1965, 1966; SOROKIN 1967; IRWING 1984; PREGO et al. 1998; OTEGUI et al. 1998, 1999; SERRATO-VALENTI 1998). However, few researchers have evaluated tropical species seeds. This work sought to correlate light microscopy data through histochemical and polarized light techniques and investigations under transmission electron microscopy to characterize the reserve materials in C. peltophoroides Benth. (Leguminosae-Caesalpinoideae) cotyledons, popularly known as "sibipiruna", a tropical tree species with wide distribution in Brazil, occurring from the Southeast region, in the Atlantic forest, to the Pantanal in Mato-Grosso State (LORENZ I 2002).

2. MATERIALS AND METHODS

This work was accomplished at the Plant Anatomy Laboratory, of the Department of Plant Biology and at the Microscopy and Microanalyses Center of the Universidade Federal de Viçosa (UFV)-MG, Brazil. Ripe Caesalpinia peltophoroides Benth. seeds collected in the municipal district of Viçosa, Minas Gerais, Brazil were used for the study.

2.1. Light microscopy

Cotyledons, fresh or fixed for 72 hours in FAA50 (formalin 5: acetic acid 5: 50% ethyl alcohol 90) were stored in 70% ethanol (JOHANSEN 1940) and transversally sectioned in a table-microtome (LPC Rolemberg e Bherring). The material embedded in methacrylate (Leica Historesin), according to the manufacturer's recommendations, was transversally sectioned in a rotate microtome (Spencer 820), with 7µm thickness. The histochemical tests used were: periodic acid /Schiff (PAS) reagent for polysaccharides with vicinal glycol groups (FEDER and O'BRIEN 1968), Ruthenium red for pectins (JOHANSEN 1940), Lugol for starch (JOHANSEN 1940), Alcian blue for acid mucopolysaccharides (PEARSE 1980), mercuric bromophenol blue (MAZIA et al. 1953) and xylidine Ponceau (VIDAL 1977) for proteins, Sudan III and Sudan black B for lipids (JOHANSEN 1940), Nile blue sulphate for acid and neutral lipids (CAIN 1947), rubeanic acid for fatty acids (GANTER and JOLLÉS 1970), osmium tetroxide for unsaturated lipids (GANTER and JOLLÉS 1970, 1969), ferric trichloride for phenolic compounds (JOHANSEN 1940), hydrochloric vanillin for tannins (MACE and HOWELL 1974), Wagner reagent (FURR and MAHLBERG 1981), Dittmar reagent (FURR and MAHLBERG 1981) and Dragendorff reagent (SVENDSEN and VERPOORTE 1983) for alkaloids, Nadi reagent for essential oils and oleoresins (DAVID and CADE 1964), anthimonium trichloride for steroids (MACE et al. 1974), sulphuric acid (GEISSMEN and GRIFFIN 1971) and Abraham reaction (CANIATO et al. 1989) for sesquiterpenic lactones, 2-4-dinitrophenylhydrazine for terpenoids (GANTER and JOLLÉS 1970, 1969), and hydrochloric acid and nitric acid for calcium oxalate crystals (CHAMBERLAIN 1932). Toluidine blue O was used for metachromasy (O'BRIEN et al. 1964). Counter-staining with Lugol and polarized light were used to show the presence of anisotropic substances, especially crystals and starch (O'BRIEN and McCULLY 1981). All histochemical tests proposed were used in fresh material. To evaluate the extractive or modifying activity of the fixative and the stock solution on different compounds, the tests were also applied in fixed material. For confirmation and location of compounds present in small amounts and comparison of results, it was also used material embedded in methacrylate. Standard control procedures were carried out simultaneously. The images were obtained in light microscope (Olympus AX70), equipped with polarizing filters, photographic U-photo system, and the Spot-Basic software.

2.2. Transmission electron microscopy

Portions of cotyledons were fixed with 2.5% glutaraldehyde in 0.1M sodium phosphate buffer, pH 7.2, for 1h, at room temperature, and rinsed in the same buffer six times for 10 min. The material was postfixed in 1% sodium phosphate buffered osmium tetroxide (OsO4) for 4h, at 4ºC, and rinsed in the same buffer six times for 10 min. After dehydration in a graded ethanol series, the material was embedded in epoxy resin (Spurr). Ultrathin sections were cut with a diamond knife on a MT2-B ultramicrotome (Du Pont-Sorval), collected on Formvar-coated cupper grids and conventionally stained with uranyl acetate and lead citrate. The sections were observed with a Zeiss EM 109 electron transmission microscope at 80kV.

3. RESULTS

3.1. General features

The Caesalpinia peltophoroides cotyledons show discernible protoderm, ground meristem and procambium, where the ground meristem already presents dorsiventral differentiation, with two to three layers of elongated and juxtaposed cells in the adaxial face, resembling a palisade parenchyma, and several layers of isodiametric cells and compact arrangement on the abaxial face. Among the procambial strands, disposed along the middle region of the cotyledon, large secretory cavities stand out, quite differentiated in the ripe seed. All the cotyledonary cells present thin primary walls, pectocellulosic, stained with PAS, toluidine blue and ruthenium red (Table 1). The Alcian blue test (Table 1) indicates the presence of acid mucopolysaccharides in the external periclinal walls of protoderm cells, probably related to a higher hydrophilia of that region.

3.2. Histochemical tests

The cotyledon mesophyll is rich in reserve lipids, mainly in the cotyledon abaxial face, being intensely orange stained by Sudan IV (Fig. 1A, Table 1) and black-bluish stained by Sudan Black B (Fig. 1B, Table 1). Lipids are black stained with the OsO4 test (Fig. 1C, Table 1), characterizing unsaturated lipids, while the presence of neutral lipids is confirmed by the characteristic pink staining of Nile blue sulphate (Fig. 1D, Table 1). Free fatty acids were not found in the lipid composition with the rubeanic acid test (Table 1). All tests for lipids demonstrated similar results in fresh and fixed material. The most conclusive results were obtained in fixed material. Reserve lipids were not detected in the material embedded in methacrylate. Because fresh or fixed (without methacrylate embedded) cotyledons were sectioned for the histochemical analyses in light microscopy, lipids coalesce to form one or more oil drops in each cell (Fig. 1A-D) and can occupy over to ¼ of the cellular volume.


 








Proteins are abundant in all cotyledon mesophyll, especially in the cotyledon adaxial face. Mercury-bromophenol blue and xylidine Ponceau tests (Fig. 1E, Tab.1) confirmed their presence. Similar results were obtained for fresh, fixed or methacrylate embedded material. Among the tests used for protein, xylidine Ponceau presented the most intense and specific coloration, indicating cell compartmentalization in globoid structures, denominated protein bodies.

In the cotyledon adaxial face, the palisade parenchyma shows calcium oxalate crystalline inclusions associated to protein structures, in the form of druses, birefracting under polarized light (Fig. 1G), whose chemical composition is confirmed by its disappearance after treatment with hydrochloric and nitric acid. Fresh, fixed or methacrylate embedded material was suitable to observe crystals under polarization, but the tests were only possible in material without embedding.

Starch, black stained by Lugol and couterstained with toluidine blue (Fig. 1F), is found in small amounts, but distributed throughout the cotyledon mesophyll, with weak birefraction under polarized light. The presence and distribution of starch in the cotyledons were better determined in material embedded in methacrylate, stained with lugol (Table 1) or PAS (not shown). Lipids and proteins were also observed in small amounts in the protoderm.

The presence of alkaloids and terpenoids was not detected (Table 1) in the whole cotyledon mesophyll. Phenolic compounds in both fresh and fixed materials were only found in the secretory cavities, indicated by a characteristic greenish color of the material embedded in methacrylate and stained with toluidine blue and with the black color of ferric chloride (Fig. 1H, Table 1). Tannins were not detected with the hydrochloric vanillin test (Table 1). The epithelium of the secretory cavities and adjacent cells are rich in lipids, proteins and starch, positively reacting to the specific tests (Table 1).

Although the usual recommendation for the histochemical analyses is the use of fresh material, the material fixation in FAA50 did not modify qualitative or quantitatively the reserve materials such as lipid, protein and starch, or even crystals and phenolic compounds, when observed under light microscopy. The embedding in methacrylate was not suitable only for the lipid analysis. However, it was more conclusive for the observation of amyloplasts and crystals, due to their small sizes in this species.

3.3. Ultrastructure of storage cells

Lipids are compartmentalized in small round organelles, called lipid bodies, varying in size from 0.5 to 1.5µm. They are abundant and evenly distributed over all the cytoplasm and have radiated disposition around the protein bodies (Fig. 2A-F).


 






C. peltophoroides protein bodies have a 5-15µm diameter, with electron dense protein matrix, and globoids with variable size and number. Great crystalline inclusions are observed in the protein bodies. However, they are lost during material processing, leaving only their contour in form of druses. Crystals are only observed in the protein bodies located in the palisade parenchyma, and usually only one druse is found in each protein body.

The starch grains have up to 1µm and irregular shape. They are found in 2-4µm plastids, with different stroma and lamellar system, where the thylakoid piling can be seen.

4. DISCUSSION

Among the lipids, oils and fats are the main forms of storage of reduced carbon in seeds, mainly as triacylglycerides, that are neutral lipids in which the fatty acid molecules are linked to the three hydroxyls of the glycerol groups by ester bonds. In the plant lipids, the main saturated fatty acids are lauric, miristic, palm and stearic acids. The main unsaturated fatty acids, oleic, linoleic, and linolenic acids, and their proportion in lipids vary with the species (BUCHANAN et al. 2000). The triacylglycerides are stored in the cotyledon cells cytoplasm or in reserve tissues, organelles known as oleosomes, spherosomes (SOROKIN 1967; FAHN 1985), oil bodies (HORNER and ARNOTT 1965; HUANG 1992; BUCHANAN et al. 2000) or lipid bodies (MURPHY 1990; PREGO et al. 1998; OTEGUI et al. 1999). In lipid bodies, the triacylglycerides are surrounded by a membrane consisting of one layer (monolayer) of phospholipids, stabilized by oleosins, special proteins that recover the surface and hinder the fusion of phospholipids from adjacent lipid bodies (MURPHY 1990; HUANG 1992). Triacylglyceride biosynthesis is attributed to enzymes present in cytoplasm membranous compartments, where the lipid accumulates between two phospholipidic membrane layers, which intumesce and separate as more material is added, releasing a new lipid body that is finally covered by a layer of oleosins formed by the rough endoplasmatic reticulum (MURPHY 1990). In Myrsine laetevirens seed endosperm, the genesis of lipid bodies takes place through the smooth endoplasmatic reticulum secretion, in close association with mitochondrias and plastids, although the rough endoplasmatic reticulum and Golgi are also present (OTEGUIet al. 1999). In C. peltophoroides cotyledons, the diameter of the lipid bodies varies from 0.5 to 1.5µm. Its uniform distribution over the cytoplasm (Fig. 2) and radiated disposition in relation to the protein bodies is similar to Yucca (HORNER and ARNOTT 1965), Myrsine laetevirens (OTEGUI et al. 1999) and Chenopodium quinoa (PREGO et al. 1998) seeds. However, the diameters of these structures measured from transmission electron micrographs are usually underestimated, since most lipid bodies are not viewed at their equatorial planes but rather at planes randomly cut through the organelles.

In seeds, the protein bodies or protein vacuolum accumulate proteins and soluble carbohydrates, in which the most common proteins are globulins, found in embryos, and prolamines, exclusive for cereal endosperm, and both function as amino acid reserves. The mechanisms and organelles involved in protein formation, transport and accumulation in seeds are extensively discussed, usually involving the Golgi complex route (MARTY 1999). In M. laetevirens, rough endoplasmatic reticulum and Golgi are particularly evident during the deposition of proteins in the endosperm, and the protein bodies originate of pre-existent vacuoles or derive directly from Golgi vesicles, where proteins from the matrix are added after the complete crystalloid deposition (OTEGUI et al. 1999). Crystalloids are absent in the protein bodies of C. peltophoroides cotyledons. However, electron-transparent globoids associated to the protein matrix occur and, when this the case, they have variable number and size (Fig. 2A-C), corresponding to the protein bodies types A, D, E, I and J, as proposed by Lott (1981). The globoids or crystal globoids are electron-dense inclusions that constitute the main mineral reserves in seeds, with high phytin concentration and, therefore, accumulating inositol and phosphorous, besides other cations, such as potassium, calcium, iron, manganese, magnesium and barium (LOTT 1981). Other authors indicate globoids as electron-transparent areas (BAGLEY et al. 1963; HORNER and ARNOTT 1965; KUANG et al. 2000) or as clear areas left by the globoids after their elimination during sectioning (PREGO et al. 1998). The average diameter of C. peltophoroides protein bodies (5-15µm) measured from light (Fig. 1E) or electron micrographs (Fig. 2A) might be underestimated, exactly as it happens with lipid bodies, since they are randomly sectioned, and not necessarily on their equatorial axis.

Crystalline inclusions in the form of calcium oxalate druses are observed in protein bodies, but only in those present in the ground meristem cells designed to be transformed into palisade parenchyma. According to Lott (1981), druse crystals in protein bodies may be common in some species, and their presence can vary depending on the cell and on the tissue. Generally, only one druse is present in each protein body in C. peltophoroides (Fig. 2B), but, in some cells, up to two druses are observed. Observations under light microscopy indicate the chemical nature of the calcium oxalate druses, by the birefraction under polarized light and by the fast dissolution with acids. Although starch, protein, lipid and crystals are generically denominated ergastic or reserve substances (FAHN 1985 DICKISON 2000), commonly found in the endosperm and in the embryo of seeds of several species, crystals present in protein bodies are not actually used during the embryo development or germination process (OTEGUI et al. 1998, 1999; SERRATO-VALENTI et al. 1998; CORTE 2005). Although calcium oxalate crystals represent good taxonomic characteristic (LOTT 1981), their function is still discussed (TILLMAN-SUTELA and KAUPPI 1999; FRANCESCHI and NAKATA 2005). P. tanacetifolia endosperm presents calcium oxalate crystals and globoids rich in calcium in the protein bodies. Nevertheless, during germination only the globoids are digested. In this case, the calcium used by the seedling during the initial development does not come from the calcium oxalate crystals, but only from the globoids (SERRATO-VALENTI et al. 1998).

Starch is a polymer formed by the association of two polysaccharide types, amylose, usually present in the proportion of 25% and amylopectin, in the proportion of 75%. In some cases, this rate can be significantly changed (MORRISON 1992). In chloroplasts, starch grains are temporary because they are quickly degraded after formation, while in the leucoplasts, they are larger, varying from 1 to 150 µm, and stay for a long period in reserve organs (DICKISON 2000). The occurrence of starch grains in Papilionatae seeds is considered abundant, rare in Mimosoidae, and absent in the known Caesalpinioideae (CORNER 1976). In Caesalpinia peltophoroides cotyledons, starch grains are present (Fig. 2A, E-F) in small amounts, with about 1µm and irregular shape, occupying a small plastid area, where they occur. In these plastids, the presence of piled thylakoids, associated to small starch grains (Fig. 2E-F), can also indicate a transitional form that would result in the conversion to chloroplasts after germination. The radial disposition of the starch around an initial polymerization point, the hilum, confers crystalline properties to the starch grains (FAHN, 1985). Under polarized light, as a result of the double light refraction when crossing the starch grain, an interference cross-shaped figure is usually formed (DICKISON 2000). In C. peltophoroides, due to the irregular shape and reduced size of the starch grains, the birefraction under polarized light is not observed and, consequently, the typical interference figures are not formed. Starch grains are accumulated in plastids during the initial endosperm development of Myrsine laetevirens, and gradually disappear while protein and lipid bodies are formed (OTEGUI et al. 1999). They are absent in the ripe endosperm, representing a temporary form of reserve (OTEGUI et al. 1998).

In general, plant secretions are complex and formed by numerous compounds (ASCENSÃO and PAIS 1987; ASCENSÃO et al. 1997, 1999; SERRATO-VALENTI et al. 1997). Therefore, there can be a predominance of a chemical group, as in the case of the phenolic compounds present in the secretory cavities of C. peltophoroides, which suggests some specificity in the cell secretory activity. Because of the presence of chemical defenses such as the phenolic ones, the secretory cavities could have an ecological role related to the deterrence of predators and fungi and bacterium parasites (FAHN 1985; VAZQUEZ-YANES and OROZCO-SEGOVIA 1993; HARBORNE 1997), assuring the species reproduction.

5. CONCLUSIONS

Concluding, the major reserve materials of C. peltophoroides cotyledons are lipids and proteins, compartmentalized in lipid bodies and protein bodies, respectively. However, small amounts of starch are found in plastids.

6. ACKNOWLEDGEMENTS

V.B. Corte is grateful to the CNPq (Conselho Nacional de Desenvolvimento Científico e Tecnológico) for the financial support.

7. REFERENCES

Recebido em 14-12-2007 e aceito para publicação em 23.06.2009.

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Publication Dates

  • Publication in this collection
    04 Mar 2010
  • Date of issue
    Oct 2009

History

  • Accepted
    23 June 2009
  • Received
    14 Dec 2007
Sociedade de Investigações Florestais Universidade Federal de Viçosa, CEP: 36570-900 - Viçosa - Minas Gerais - Brazil, Tel: (55 31) 3612-3959 - Viçosa - MG - Brazil
E-mail: rarvore@sif.org.br