PLANT BREEDING, GENETIC RESOURCES & MOLECULAR BIOLOGY

Rooting of two types of cuttings of fruit crops Vaccinium floribundum Kunth and Disterigma alaternoides (Kunth) Niedenzu (Ericaceae)

Enraizamiento de dos tipos de estacas de los frutales Vaccinium floribundum Kunth y Disterigma alaternoides (Kunth) Niedenzu (Ericaceae)

Stanislav Magnitskiy ¹,³,Gustavo Ligarreto M.¹, and Héctor Orlando Lancheros²

Vaccinium floribundum Kunth and Disterigma alaternoides (Kunth) Niedenzu are two fruit-bearing species of the family Ericaceae, native to the Andean forest. Given very scarce knowledge on their ecophysiology, it is not known how to propagate these plants, which limits the possibility of introducing these into the commercial culture. The present study had an objective to evaluate the rooting potential of softwood and hardwood cuttings of V. floribundum and D. alaternoides using 50-400 mg L^-1 naphthaleneacetic acid (NAA) and indole-3-butyric acid (IBA) as rooting hormones in an organic-mineral medium. The softwood cuttings taken from the apical part of the branch had up to 47.0% rooting in V. floribundum and up to 77.2% in D. alaternoides at day 60, whereas hardwood cuttings taken from the base of the branch presented lower rooting values, among 8.1 and 24.0% in V. floribundum and among 6.8 and 34.5% in D. alaternoides. Softwood cuttings of V. floribundum y D. alaternoides treated with 400 mg L^-1 mg NAA remained viable up to 64 and 86%, while the rooting percentage was up to 44.4 and 77.2 %, and average number of roots was up to 8.4 and 6.3, respectively. The results of the study offer a base for development of the protocol for the vegetative propagation of these species. Vaccinium floribundum Kunth y Disterigma alaternoides

Key words: propagation, mortiño, ovo, auxins, indole-3-butyric acid, 1-naphthaleneacetic acid.

RESUMEN

(Kunth) Niedenzu son dos especies frutales de la familia Ericaceae, nativas del bosque andino. Dado el muy escaso conocimiento divulgado sobre su ecofisiología, no se conoce como propagar estas plantas, lo que limita la posibilidad de introducirlas como cultivo comercial. El presente estudio tuvo como objetivo evaluar el potencial de enraizamiento de las estacas jóvenes y semileñosas de V. floribundum y D. alaternoides utilizando 50-400 mg L^-1 del ácido naftalenacético (ANA) y del ácido indolbutírico (AIB) como hormonas enraizadoras en un sustrato orgánico-mineral. Las estacas jóvenes provenientes de primordios apicales de la rama tuvieron hasta 47,0% de enraizamiento en V. floribundum y hasta 77,2% en D. alaternoides al día 60, mientras que estacas semileñosas provenientes del tercio medio de la rama presentaron más bajas tasas de enraizamiento, entre 8,1 y 24.0% en V. floribundum y entre 6,8 y 34,5% en D. alaternoides. Las estacas jóvenes de V. floribundum y D. alaternoides tratadas con 400 mg L^-1 de ANA permanecieron viables hasta 64 y 86% respectivamente, mientras que el porcentaje de enraizamiento fue de 44,4 y 77,2% y el número promedio de las raíces fue de 8,4 y 6,3. Los resultados del estudio ofrecen una base para la elaboración del protocolo de la propagación vegetativa de estas especies.

Palabras clave: propagación, mortiño, ovo, auxinas, ácido indolbutírico, ácido naftalénacético.

Vaccinium floribundum Kunth and Disterigma alaternoides (Kunth) Niedenzu are two fruit species of tribe Vaccinieae of family Ericaceae native to the Andean forest. In the neotropics, several fruit species of this family have a potential to be cultivated, such as Vaccinium meridionale, Gaultheria anastomosans, and Macleania rupestris that grow spontaneously in the north-western South America. Most of these species in the Andean region may be found in cold, wet and mountainous habitats located between 1,500 and 3,000 m a.s.l. (Luteyn, 2002) as shrubs, epiphytes and, occasionally, lianas (Gentry, 1996; Luteyn, 2002).

Vaccinium is the largest genus of the tribe Vaccinieae (Lens et al., 2002). In case of V. floribundum, this plant has its natural distribution in Venezuela, Colombia, Ecuador, Peru (Luteyn, 2002), Costa Rica (Schneidt et al., 1996), and Bolivia (Sanjinés et al., 2006). This fruit bearing plant may be encountered in páramos of the Andes from 2,700 (Salzer et al., 2006) up to 4,000 m a.s.l. (Schick, 1993). V. floribundum is a shrub with height ranging among 2.0 and 3.5 m (Schick, 1993; Sanjinés et al., 2006), although in the mountains of Cundinamarca dwarf plants from about 20 cm height could be found in a state of fruiting. The fruit of V. floribundum is a spherical berry of 5-12 mm in diameter, its color varies from blue and dark blue, with surface smooth and sometimes glaucous (Sanjinés et al., 2006). In mountain forests of Colombia, this plant often grows in association with V. meridionale and D. alaternoides and could be distinguished from these species by lower size, leaves of dark green color with crenulate margins, dense branching, and berry of more acid flavor.

V. floribundum is a commonly used species, especially in Ecuador, to prepare marmalades, drinks and desserts (Luteyn, 2002; Vasco et al., 2009). Its high content of anthocyanins, reaching 345 mg/100 g FW (Vasco et al., 2009) as well as high accumulation of phenolics and vitamin C in fruits makes these stand out for their medicinal properties, mainly for treatment of cardiovascular problems and cancer (Schreckinger et al., 2010).

In Colombia, V. floribundum is known under the names of agracejo, mortiño, mortiño de árbol (Antioquia), agraz, chivaco (Cundinamarca) (Cardozo et al., 2009). It is one of five native species of the genus Vaccinium reported so far in Colombia: V. meridionale, V. floribundum, V. corymbodendron, V. euryanthum, and V. singularis (Salinas and Betancur, 2007). It is worth mentioning that V. meridionale and V. floribundum are traditionally considered the only two native species of this genus, whose fruits are edible (Schick, 1993), although the reports exist that V. corymbodendron also has edible fruits (Sierra et al., 2005). V. corymbodendron grows in the same environments that V. floribundum and V. meridionale (Marcano-Berti, 2002) and is mistaken in its natural habitat with other Ericaceae species Disterigma alaternoides and Gaultheria myrsinoides. The confusion between the species comes from the lack of knowledge on the morphological differences between them in the field and the use of a common terminology, because the name "mortiño" in the Andean region is used for a wide variety of plants, including V. corymbodendron (Sierra et al., 2005), V. meridionale (Schick, 1993), V. floribundum (Vasco et al., 2009), Hesperomeles sp. (Gentry, 1996; Cardozo et al., 2009) and other species.

The genus Disterigma s.l. holds up to 40 species, mainly small shrubs distributed in the forests of high mountains and páramos from southern Mexico (Wilbur, 1992) to Central America and northern South America (Pedraza- Peñalosa, 2009; Pedraza-Peñalosa, 2010). Information on the distribution, physiological and horticultural potential of D. alaternoides is much more limited than that of V. floribundum. In South America, the plant grows spontaneously in Venezuela, Colombia, Ecuador, Peru, Guyana, and Bolivia at altitudes between 2,400 and 3,700 m a.s.l. (Smith, 1933), often in associations with other Ericaceae. It is a shrub that reaches up to 4.0 m height (Smith, 1933) with edible fruits of bitter taste characterized by a high content of flavonoids (Pino et al., 2001). The fruits are rounded translucent berries with size between 5 and 12 mm in diameter and color ranging from white-pink to red. In Colombia, D. alaternoides is also known as capulí silvestre (Nariño), uvo blanco, and ovo grows in páramos of North Santander, Cundinamarca, Nariño (Smith, 1933), Chocó (Pino et al., 2001), and Boyacá. Its use for food in Colombia appears to be limited and includes fresh fruit consumption as well as processed cakes and marmalades, the latter presentation is most commonly used modality in Sumapaz, rural town of Bogotá.

Given the lack of reported knowledge about the species under discussion, there is no reference to suggest the development of programs dedicated to the domestication of these species. In particular, it is not known how to propagate these plants, which limits the possibility of introducing these as commercial crops. For V. floribundum, some questions of propagation by cuttings (Noboa, 2010) and seeds (Cardozo et al., 2009) were answered, the last one is slow, erratic and propagules are very non-uniform and apparently have high genetic diversity; there were, no published data found on the propagation of D. alaternoides. There is a need to develop a protocol for the propagation of these species. Taking into account that different ericaceous plants are often multiplied by cuttings, the present study was done to evaluate the potential of rooting of cuttings of two species of Ericaceae using indolebutyric and naphthaleneacetic acids as rooting hormones to provide a recommendation to potential farmers in the establishment of plants in culture selected for their production, fruit quality, and other desirable characteristics.

Materials and methods

The study was conducted in greenhouse under plastic cover at the Faculty of Agronomy, Universidad Nacional de Colombia, Bogota. The material of V. floribundum and D. alaternoides was obtained from branches cut from shrubs in Choachí, Cundinamarca. The plants of V. floribundum with an average height of 30 cm were obtained at the site located at coordinates 35' 17.2" W and 73° 59' 53.1" N, altitude 3,348 m a.s.l.; the plants of D. alaternoides with an average height of 1.30 m were obtained at the site located at coordinates 36' 12.2" W and 73° 58' 02.2", altitude 3,200 m a.s.l. The vegetation at both sites corresponded to páramo, with the presence of low-and medium-sized shrubs of Ericaceae and Melastomataceae. Mother plants to select the cuttings were the adult ones, with the appearance of some fruits and without visual symptoms of nutritional deficiencies or phytosanitary problems. Orthotropic vegetative branches were used to prepare the cuttings with similar characteristics, with turgid leaves and of good vigor. For both species were used two types of cuttings: young taken from apical primordia and semi-hardwood taken from the middle third of the branch. The characteristics of the cuttings are presented in Tab.1.

Rooting was carried out with different concentrations of auxins, indolebutyric acid IBA and naphthaleneacetic acid NAA. The hormone solutions were prepared taking 2,000 mg IBA (Sigma, Ontario, Canada) or 2,000 mg NAA (Sigma, Ontario, Canada) pure, diluted in 10 mL of 70% ethyl alcohol and adding distilled water to volume one liter. From these solutions, solutions of 0, 100, 400 and 800 mg L^-1 of IBA or NAA were prepared, doses that were mixed with industrial talc. The mode of application of the hormones was to perform a mixture of the solution of the hormone with talc as inert material in such a proportion to produce a paste containing 0, 50, 200 or 400 mg L^-1 IBA or NAA (Castrillón et al., 2008). This method allows the hormone remaining at the base of the cutting any longer when compared with a dip of the cutting in hormone solutions, often of very high concentration (Castrillón et al., 2008; Ávila Díaz-Granados et al., 2009). Approximately 1 cm of the basal part of the cuttings were introduced into the mixture and allowed drying at ambient temperature for 1-2 min, then sown in plastic trays of 18 alveoli with diameter 8.0 cm and depth 8.0 cm. As rooting medium was used organically-mineral substrate composed of peat without mineral nutrients (Klasmann-Deilmann GmbH, Geeste-Germany) mixed in a 1:1 ratio with coal ash consisting of residues of medium structure. The mixture with peat present physical condition to maintain aeration and water retention in substrate avoiding problems of low water retention in the substrate of coarse ash or pure peat or poor drainage in the substrate of fine ash (Castrillón et al., 2008). In order to water the cuttings, water mist was supplied for 10 min twice a day during the first 30 d; after 30 d and until the end of the experiment the frequency of watering was once a day. The trays were kept covered with plastic after applying irrigation to reduce temperature changes on rooting bench and reduce transpiration by leaves/stem keeping alive the cuttings up to the time than these formed adventitious roots. A synthetic black mesh was installed providing 75% light on the bench, to reduce the intensity of solar radiation and to maintain high relative humidity during the rooting.

At 60 d, the following variables were measured: percentage viability of cuttings estimated by the presence of at least two leaves, percentage of cuttings rooted from total cuttings planted, number of adventitious roots, and average length of the roots on each cutting. We used a completely randomized design with 14 treatments, consisting of two hormones, IBA and NAA, three hormone concentrations and two types of cuttings, young and semi-hardwood, the control was distilled water. Each treatment consisted of 16 replicates. An analysis of variance was done using the statistical package SAS® version 9 and the differences between treatments were evaluated by Tukey test.

Results

From day 14 after start of the experiment some cuttings of Vaccinium floribundum and Disterigma alaternoides began to show symptoms of viability loss, recorded by leaf abscission. The fall of leaves was accompanied by necrosis of the cuttings that began in the basal end and was progressively moving toward the apex.

In general, the rooting of cuttings was more successful in D. alaternoides than in V. floribundum (Tab.2 and 3). D. alaternoides had adventitious root formation not only at the base of the cuttings, but also at the leaf base, which was not typical for V. floribundum (Fig.1). When transplanting some control cuttings at day 60 in the pots filled with the same organic-mineral substrate, plants of D. alaternoides had intensive growth of new shoots within next 2 to 4 months, while the growth of V. floribundum growth was slow (data not shown).

In V. floribundum, mortality rate of young cuttings was high; in most treatments, except NAA applications of 200 and 400 mg L^-1, for 60 days more than half of young cuttings died (Tab.2). More lignified cuttings remained viable for longer than the tender cuttings, possibly due to a lower rate of drying off. Woody cuttings of V. floribundum thicker than those present in the study were viable for a longer time, they sprouted but did not emit roots (data not shown), the results were similar to those observed in V. meridionale (Ligarreto et al., 2006) when highly lignified cuttings had very low rhizogenic activity. At the same time, the percentage of rooting was higher in young cuttings than in lignified ones (Tab.2).

The application of NAA to the cutting base favored rooting of cuttings, increase of number and length of roots, while the IBA had a minor effect. Young cuttings of V. floribundum treated with 200 and 400 mg L^-1 NAA remained viable up to 56 and 64%, respectively, the rooting percentage was 47 and 44%, and the average number of roots was 7.0 and 8.4 that proves the usefulness of these treatments to propagate this species. The average length of roots increased significantly in young cuttings by treating these with 400 mg L^-1 NAA, whereas treatment with 400 mg L^-1 IBA did not cause the same effect (Tab.2).

In case of D. alaternoides, it was shown higher percentage of viability of both types of cuttings compared with V. floribundum (Tab.2 and 3). By comparing the percentages of rooting of young and semi-hardwood cuttings, the first ones had higher rooting in D. alaternoides. The cuttings taken from the middle third of the branch remained viable for longer time than apical cuttings. Over 90% of young cuttings of D. alaternoides in all treatments, that remained alive at 60 d after the start of the experiment, formed adventitious roots (Tab.3). The application of rooting hormones (400 mg L^-1 NAA or IBA) increased the number of rooted cuttings and the number and length of roots formed, this effect was more evident in the young cuttings than in semihardwood cuttings.

Discussion

The results show that the multiplication of Disterigma alaternoides by cuttings has higher potential because it is rooted more easily than Vaccinium floribundum. The rate of woody plant regeneration after cutting as the cause of pruning, forest fires, etc., and the ability to produce adventitious roots are a feature of indirect activity of endogenous auxins (Hartmann et al., 1996). Although these two species often form associations in páramos of the Andes, the results indicate that their rates of vegetative propagation in their natural habitat might be different.

Lignified cuttings of both species remained viable for more time than young cuttings, which could be attributed to the effect of their thickness. The lignified cuttings were thicker and should have contain more carbohydrate reserves to remain viable; additionally, a high degree of lignification might prevent rapid drying of the thick cuttings (Hartmann et al., 1996), therefore, the young Ericaceae cuttings are more demanding in watering conditions than the lignified ones (Giroux et al., 1999 and references therein). On the other hand, the rooting percentage was higher in young cuttings, with the presence of apical bud, as it was proven in other ericaceous (Gough, 1993; Lee et al., 2004; Yong et al., 2005). High percentage of rooting in young cuttings, especially D. alaternoides, might be due to endogenous auxin activity, taking into account that the apical and axillary buds are a source of auxin for callogenesis and rhizogenesis (Hartmann et al., 1996). In this context, the length of cuttings may be important for rooting, with Vaccinium angustifolium cuttings of high number of nodes, 4 to 6, were more successful for rooting than short cuttings (Lee et al., 2004). Moreover, the growth of adventitious roots in woody cuttings could be prevented by sclerenchyma (Hartmann et al., 1996), a tissue whose formation tends to be increasing with the age of plant organs. For example, in hardwood cuttings of Vaccinium corymbosum, continuous layer of lignified pericycle fibers and the epidermis affected the emergence of adventitious roots that originated from the cambium and the phloem (Mahlstede and Watson, 1952).

Blueberries like other Ericaceae are typically propagated by stem cuttings (Horigome et al., 2008, Trevisan et al., 2008), although these are known to be very hardrooted when multiplied by this method. Their rates of rooting are low and time for emission of adventitious roots goes beyond 3 to 4 weeks (Gough, 1993), therefore, auxin applications tend to increase the percentage of rooting in cuttings (Debnath, 2007; Fischer et al., 2008; Ávila Díaz-Granados et al., 2009).

Among auxins, IBA and NAA are used to induce rooting because these are non-toxic in a wide range of concentrations for a large number of species and chemically stable in contact with the substrate of propagation (Hartmann et al., 1996). Auxin applications had more effect on rooting of apical cuttings than on those taken from the middle part of the branch, as was observed in Vaccinium ashei (Schuch et al., 2007). Additional treatments to stimulate adventitious root formation in cuttings of ericaceous include: the increase of luminosity in the rooting chamber because darkness may reduce the percentage of rooting (Yong et al., 2005, Damiani et al., 2009), increase in the level of CO2 in the rooting chamber between 0.1% (Prokaj et al., 2004) and 5% (Biggs et al., 1983) and warming the rooting bench (Horigome et al., 2008; Luna, 2009). Other factors, whose effect could be evaluated for stimulating the rooting are the composition and characteristics of the substrate (Hoffmann et al., 1995; Castrillón et al., 2008), the type of cut made in the cutting (Trevisan et al., 2008), the insertion depth of the cutting into the substrate (Horigome et al., 2008), and the polarity of the cutting.

The use of cuttings for commercial propagation can significantly reduce the time Ericaceae require for the establishment of cultivated plants compared with other propagation methods, such as in vitro (Albert et al., 2009), thus, the cuttings of D. alaternoides and V. floribundum as propagating material offer gain in time of culture establishment and fruiting. It is noteworthy that many neotropical Ericaceae in their natural habitat are propagated by rhizomes (genera Lyonia, Pernettya, Tepuia, and Themistoclesia) or adventitious roots that form along the stems (genus Disterigma) (Luteyn, 2002). In different ericaceous, extensive systems of rhizomes can form large clonal colonies, such as in Disterigma empetrifolium, while the stems of some species of the genera Arbutus, Ceratostema, Comarostaphylis, Macleania, and Vaccinium have lignotubers, in where meristematic areas are located with high capacity for regeneration after cuttage (Luteyn, 2002; Evans and Vander Kloet, 2010). The diversity of organs used for multiplication provides a possibility to use these materials for the propagation of the species studied. In practical terms, at 400 mg L^-1 NAA promises more than 44% (V. floribundum) and 77% (D. alaternoides) rooting of cuttings taken from apical branch primordia, which serves as a base for developing a protocol for vegetative propagation of these plants under greenhouse conditions.

Conclusions

The research results show that young cuttings have high rooting potential in V. floribundum and, especially, D. alaternoides, which may be useful as a method of vegetative propagation of these species. The percentage of rooting of semi-hardwood cuttings did not exceed 24.0 (V. floribundum) and 34.5% (D. alaternoides) at 60 d after starting the experiment and their use for propagation is limited. Exogenous auxin application to the base of young cuttings increased the viability, percentage of rooting, and number and length of roots formed. In practical terms, 400 mg L^-1 NAA promises more than 44% (V. floribundum) and 77% (D. alaternoides) rooting of cuttings taken from apical primordia of the branches.

Acknowledgements

The authors express their gratitude to Dr. Paola Pedraza- Peñalosa (Institute of Systematic Botany, The New York Botanical Garden, USA) for her valuable assistance in the taxonomic determination of material D. alaternoides for this study.

Literature cited

Albert, T., M. Starast, K. Karp, H. Kaldmäe, E. Vool, and T. Paal. 2009. The influence of propagation method on growth of the Half-Highbush blueberry 'Northblue'. Acta Hort. 812, 141-145.

Ávila Díaz-Granados, R.A., O.J. Orozco Silva, G.A. Ligarreto Moreno, S. Magnitskiy, and A. Rodríguez. 2009. Influence of mycorrhizal fungi on the rooting of stem and stolon cuttings of the Colombian blueberry (Vaccinium meridionale Swartz). Int. J. Fruit Sci. 9, 372-384.

Biggs, R.H., P.G. Webb, and S.V. Kossuth. 1983. Rooting characteristics of eight rabbiteye blueberries recommended for Florida. Proc. Fla. State Hort. Soc. 96, 228-229.

Cardozo, R.H., S.L. Córdoba, J.D. González, J.R. Guzmán, H.O. Lancheros, L.I. Mesa, R.A. Pacheco, B.A. Pérez, F.A. Ramos, M.E. Torres, and P.T. Zúñiga. 2009. Agracejo. pp. 57-68. In: Guzmán, J.R., S.L. Córdoba, P.T. Zúñiga, M.E. Torres, B.A. Pérez, L.I. Mesa, R.A. Pacheco, and C. Córdoba (eds.). Especies útiles de la región Andina de Colombia. Vol. I. Jardín Botánico de Bogotá José Celestino Mutis. Bogota.

Castrillón, J.C., E. Carvajal, G. Ligarreto, and S. Magnitskiy. 2008. El efecto de auxinas sobre el enraizamiento de las estacas de agraz (Vaccinium meridionale Swartz) en diferentes sustratos. Agron. Colomb. 26, 16-22.

Damiani, C.R., T.R. Pelizza, M.W. Schuch, and A. De Rossi Rufato. 2009. Luminosidade e IBA no enraizamento de microestacas de mirtileiro dos grupos Rabbiteye e Southern Highbush. Rev. Bras. Frutic. 31, 650-655.

Debnath, S.C. 2007. Influence of indole-3-butyric acid and propagation method on growth and development of in vitro and ex vitro-derived lowbush blueberry plants. Plant Growth Reg. 51, 245-253.

Evans, R.C. and S.P. Vander Kloet. 2010. Comparative analysis of hypocotyl development in epiphytic, lignotuber-forming, and terrestrial Vaccinieae (Ericaceae). Botany 88, 556-564.

Fischer, D.L.O., J.C. Fachinello, A.L.E. Correa, T.Z.F. Pinto, and C.L. Giacobbo. 2008. Efeito do ácido indolbutírico e da cultivar no enraizamiento de estacas lenhosas de mirtilo. Rev. Bras. Frutic. 30, 285-289.

Gentry, A.H. 1996. A field guide to the families and genera of woody plants of northwest South America (Colombia, Ecuador, Peru) with supplementary notes on herbaceous taxa. The University of Chicago Press, Chicago, IL.

Giroux, G.J., B.K. Maynard, and W.A. Johnson. 1999. Comparison of perlite and peat:perlite rooting media for rooting softwood stem cuttings in a subirrigation system with minimal mist. J. Environ. Hort. 17, 147-151.

Gough, R.E. 1993. The highbush blueberry and its management. CRC Press, New York, NY.

Hartmann, H.T., D.E. Kester, F.T. Davies, and R. Geneve. 1996. Plant propagation principles and practices. 6th ed. Prentice Hall, New York, NY.

Hoffmann, A., J.C. Fachinello, and A.M. Santos. 1995. Enraizamiento de estacas de duas cultivares de mirtilo (Vaccinium ashei Reade) em diferentes substratos. Rev. Bras. Agroc. 1, 22-30.

Horigome, M., T. Araki, T. Okada, M. Hatakeyama, and I. Kenmochi. 2008. Effect of hardwood cuttage on the propagation of blueberry (Vaccinium). Bull. Gunma Agr. Tech. Cent. 5, 33-39.

Lee, J.G., J.N. Lee, E.H. Lee, and B.Y. Lee. 2004. Cutting propagation efficiency of Lowbush blueberry (Vaccinium angustifolium Ait.) depending on the conditions of media and cutting. HortScience 39, 825.

Ligarreto, G.A., C.I. Medina, M.L. Arias, L.J. Martínez, H. Corredor, J.D. Muñoz, and P. Patiño. 2006. Zonificación de las especies de agraz (Vaccinium spp.) y una aproximación de su manejo agronómico como cultivos promisorios para la zona alto andina colombiana. Faculty of Agronomy, Universidad Nacional de Colombia, Bogotá.

Lens, F., K.A. Kron, J.L. Luteyn, E. Smets, and S. Jansen. 2004. Comparative wood anatomy of the blueberry tribe (Vaccinieae, Ericaceaes. L.). Ann. Missouri Bot. Gard. 91, 566-592.

Luna, T. 2009. Vegetative propagation. pp. 153-175. In: Dumroese, R.K., T. Luna, and T.D. Landis (eds.). Nursery manual for native plants: A guide for tribal nurseries. Vol. 1: Nursery management. Agriculture Handbook No. 730. USDA Forest Service, Washington, DC.

Luteyn, J. 2002. Diversity, adaptation, and endemism in neotropical Ericaceae: Biogeographical patterns in the Vaccinieae. Bot. Rev. 68, 55-87.

Mahlstede, J.P. and D.P. Watson. 1952. An anatomical study of adventitious root development in stems of Vaccinium corymbosum. Bot. Gaz. 113, 279-285.

Marcano-Berti, L. 2002. Studies on the flora of the Guianas N° 101: New Vochysiaceae: Qualea johannabakkeri and Qualea marionii. Acta Bot. Venez. 25, 111-118.

Noboa, V.F. 2010. Efecto de seis tipos de sustratos y tres dosis de ácido naftalenacético en la propagación vegetativa de mortiño (Vaccinium floribundum Kunth). Undergraduate thesis.Natural Resources Faculty, Escuela Superior Politécnica de Chimboraso, Riobamba, Ecuador.

Pedraza-Peñalosa, P. 2009. Systematics of the neotropical blueberry genus Disterigma (Ericaceae). Syst. Bot. 34, 406-413.

Pedraza-Peñalosa, P. 2010. Insensitive blueberries: a total-evidence analysis of Disterigma s.l. (Ericaceae) exploring transformation costs. Cladistics 26, 388-407.

Pino, N., R.D. Torrenegra, and J.A. Pedroso. 2001. Estudio botánico y químico de Disterigma alaternoides (HBK) Nied. Ericaceae: Vacciniaceas. Rev. Univ. Tecnol. Choco 14, 1657-3498.

Prokaj, E., M. Saigusa, K. Kitamura, and K. Suzuki. 2004. Growth responses of blueberry softwood cuttings to atmospheric carbon dioxide enrichment. Tohoku J. Agric. Res. 54, 13-21.

Salinas, R.N. and J. Betancur 2007. Novedades taxonómicas de las Ericáceas del suroccidente de Colombia. Caldasia 29, 51-58.

Salzer, J., S. Matezki, and M. Kazda. 2006. Nutritional differences and leaf acclimation of climbing plants and the associated vegetation in different types of an Andean montane rainforest. Oecologia 147, 417-425.

Sanjinés, A.A., B. Øllgaard, and H. Balslev. 2006. Frutos comestibles. pp. 329-346. In: Moraes, M.R., B. Øllgaard, L.P. Kvist, F. Borchsenius, and H. Balslev (eds.). Botánica económica de los Andes Centrales. Universidad Mayor de San Andrés, La Paz.

Schick, C. 1993. Overview of the blueberry industry in South America. Acta Hort. 346, 27-32.

Schneidt, J., U. Stein, B. Furchheim-Weberling, S. Wiedmann, and F. Weberling. 1996. Estudios sobre formas de crecimiento de algunas especies típicas del páramo de Costa Rica. Brenesia 45-46, 51-112.

Schreckinger, M.E., J. Lotton, M.A. Lila, and E. González de Mejia. 2010. Berries from South America: A comprehensive review on chemistry, health potential, and commercialization. J. Med. Food 13, 233-246.

Schuch, M.W., A. De Rossi, C.R. Damiani, and G.C. Soares. 2007. Aib e substrato na produção de mudas de mirtilo cv. "Climax" através de microestaquia. Ciênc. Rural 37, 1446-1449.

Sierra, E.J.A., G.F. Alzate, R.H.S. Soto, R.B. Durán, and V.L.M. Losada. 2005. Plantas silvestres con potencialidad ornamental de los bosques montano bajos del oriente Antioqueño, Colombia. Rev. Fac. Nal. Agr. Medellín 58, 2651-2663.

Smith, A. 1933. The genera Sphyrospermum and Disterigma. Brittonia 1, 203-232.

Trevisan, R., R.C. Franzon, R.F. Neto, R.G. da Silva, G.E. Dias, and A.L.E. Corrêa. 2008. Enraizamento de estacas herbáceas de mirtilo: Influência da lesão na base e do ácido indolbutírico. Ciênc. Agrotec. 32, 402-406.

Vasco, C., K. Riihinen, J. Ruales, and A. Kamal-Eldin. 2009. Chemical composition and phenolic compound profile of mortiño (Vaccinium floribundum Kunth). J. Agric. Food Chem. 57, 8274-8281.

Wilbur, R.L. 1992. A synopsis of the genus Disterigma (Ericaceae: Vaccinieae) in Mexico and Central America with the description of two previously undescribed species. Bull. Torrey Botan. Club 119, 280-288.

Yong, W.C., Z. Zhen, Y. Hong, and G. Yin. 2005. Effects of lignification of cuttings from different cultivars of Vaccinium ashei on rooting capacity. J. Plant Resour. Environ. 14, 26-32.