Cereus peruvianus (Koubo) new cactus fruit for the world

Koubo-uma nova fruta para o mundo

PALESTRAS

CROP PRODUCTION

Cereus peruvianus (Koubo) new cactus fruit for the world¹

Koubo-uma nova fruta para o mundo

Yosef Mizrahi

Department of Life Sciences, Ben-Gurion University of the Negev, Beer-Sheva, Israel. E-mail: [e-mail]

ABSTRACT

Several different species of the columnar cacti of the genera Stenocereus and Pachycereus, were introduced into different semi-arid ecozones in Israel and most of these efforts were of disappointing outcomes, the only exception being the Cereus peruvianus (L.) Miller,which bore plenty of fruits, some of them of good taste. The original seeds of this plant were obtained from the late Mr. Amram (Ron) Kodish, who collected seeds from various private gardens in Southern California which bore fruits of reasonable qualities. The initial success of this species led us to initiate an intensive research study, and today it is already fruit-crop, marketed mainly in Israel under the name " Koubo" . This paper will describe our work of domestication of this new cactus fruit crop in Israel.

Index terms:Cereus peruvianus, koubo, cacti.

RESUMO

Várias espécies diferentes de cactos colunares dos gêneros Stenocereus e Pachycereus, foram introduzidos em diferentes ecozones semiáridas em Israel, a maioria desses esforços foram de resultados decepcionantes, a única exceção sendo apenas o Cereus peruvianus (L.) Miller, que tinha muitas frutas, algumas delas com gosto bom. As sementes originais desta planta foram obtidas a partir do falecido Sr. Amram (Ron) Kodish, que coletou sementes de vários jardins privados do sul da Califórnia e que haviam dado frutos de qualidades razoáveis. O sucesso inicial desta espécie nos levou a iniciar um estudo intensivo, e atualmente existe uma produção dessas frutas, comercializados principalmente em Israel sob o nome " Koubo" .

Termos para indexação:Cereus peruvianus, koubo, cacto.

INTRODUCTION

For centuries, the indigenous people of Latin America have been using the fruits of various species of columnar cacti, known to them as pitayas, for food and other applications (Pimienta-Barrios & Nobel 1994; Pimienta-Barrios, et al 1997, Ortiz-Hernández, 1999). During the past decades, we and others have been making attempts to convert these wild or semiwild cacti, known only in their country of origin, into new cacti-fruit crops and introduce them into Western and other world markets (Pimienta-Barrios & Noble 1998; Pimienta-Barrios & Noble 1995; Pimienta- Barrios & Noble 1998; Pimienta-Barrios et al 1997; Pimienta-Barrios et al 1998; Nerd et al 1990; Nerd et al 1993; Nerd & Mizrahi 2002). Several different species of the columnar cacti of the genera Stenocereus and Pachycereus, were introduced into different semi-arid ecozones in Israel, most of these efforts were of disappointing outcomes, the only exception being the Cereus peruvianus (L.) Miller,which bore plenty of fruits, some of them of good taste (Nerd et al 1990; Nerd et al 1993; Nerd & Mizrahi 2002; Weiss et al 1993). The original seeds of this plant were obtained from the late Mr. Amram (Ron) Kodish, who collected seeds from various private gardens in Southern California which bore fruits of reasonable qualities. The initial success of this species led us to initiate an intensive research study, and today it is already fruit-crop, marketed mainly in Israel under the name " Koubo".

It is noteworthy that in South Africa this introduced species is known as an invader pest (Moran & Zimmermann 1991; Olckers 2004). This paper will describe our work of domestication of this new cactus fruit crop.

Taxonomy

We originally obtained the seeds of this new crop under the scientific name of Cereus peruvianus (L.) Miller. After publishing several papers which used this name, we received responses from Brazilian researchers asserting that the plant mentioned in our papers is in fact Cereus jamacaru from the semi-arid zones of Brazil, known there by the local name of Mandacaru. Mandacaru is consumed by the local people as a wild-cactus-fruit. My colleague Dr. A. Nerd visited Brazil and brought with him seeds of C. jamacru collected from the wild near Independência, Ceará. Indeed, there is a close similarity between the two accessions but also some differences (Mizrahi & Nerd 1999; Gutman et al 2001). All C. jamacaru seedlings which we tested (several dozens), produced un-tasty almost inedible fruits. Today we believe that the C. jamacaru might be a subspecies of C. peruvianus (Gutman et al 2001). This notion was strengthened by performing crosses between the two species, which showed that the two can pollinate each other and produce viable seedlings (Gutman 2001). This compatibility is not necessarily an indication that the two are the same species, as we found that in vine-cacti inter-specific and even inter-generic crosses can produce viable offspring (Tel-Zur et al 2004; Tel-Zur et al 2011). However, it is important to note that C. jamacaru is another important genetic source for breeding. After successfully domesticating C. peruvianus in Israel, we nicknamed it "Koubo" - a name which is easy to pronounce (Fig.1).

Species characteristics, genetics and breeding.

Among several hundreds of seedlings germinated from the C. peruvianus seed batch we obtained from Mr. Amram Kodish, we found around 8 genotypes which were of good taste and selected them for further breeding. Those chosed for further breeding were also aromatic which adds a lot to the taste as we found later in our research into the fruit quality which will be discussed later (Ninio et al 2003,a & b). We found significant differences in spine length on the shoots. In the spiny genotypes the size of the spines declines with the seedling age, from 25 cm at the base of the young seedlings (old shoots) to 2-3 cm in the new emerging youngest shoots. The non-spiny genotypes have very small spines, of around 5 mm in length even on old shoots and are almost spineless at the top. The fruit itself is in all cases smooth with no spines (Figs 1, 2 & 3). Fruit flesh color is usually white (Fig. 2), while a very pale yellowish color may occur in the flesh of some genotypes. The peel color varies from shiny deepred through pinkish-yellow to yellow (Figs 1, 2 & 3). The most important characteristic after taste was fruit cracking (Fig 4). Over 95% of the seedlings had fruits which cracked before full ripening took place. For further selection we chose genotypes with either almost no fruit cracking, or minor cracking of no more than 15%. It is interesting to note that almost all of the C. jamacaru seedlings we checked did not crack and thus these clones should be considered as future parents for further breeding of new clones, to avoid the fruit cracking problem. Four of the 8 selected clones showed peel blackening sometime after harvest even though their taste was still good, reminiscent of bananas (Fig 5). These genotypes serve today mainly as pollen sources for the commercial varieties. It is very interesting to note that these sensitive clones do not show this peel blackening in the Arava valley where average summer temperatures may rise to 40ºC concomitant with 10% air humidity (unpublished data). There was no difference in fruit cracking between the Arava hot valley and other regions in Israel (Leshem et al 2003). This species can tolerate these high temperatures with no problem. However, subfreezing temperatures (-6ºC for several hours) can eradicate a whole plantation. At -2ºC some clones were heavily damaged while others survived and produced the same yield in the following summer as in normal years (unpublished data). Hence, it is possible to breed for sub-freezing tolerant varieties. Molecular typing of various genotypes analyzed by random amplified polymorphic DNA (RAPD) technique demonstrated that this species has a limited genetic base and additional germplasm is required for further efficient clone improvement (Gutman et al 2001).

The C. peruvianus species is basically self-incompatible (Weiss et al 1994). Unlike the vinecacti, not a single genotype was found to be able to pollinate itself. Another important finding is that not every genotype can pollinate others. It is reminiscent of the S1 S2 mechanism of in-compatibility which is also found in other fruit trees (Newbigin et al 1993). To guarantee fruit production throughout the year, we have to match compatible clones for early, medium and late season of flowering and fruiting clones. It is of major interest to try producing self-compatible clones by doubling the chromosomes as was done with the vine-cacti and some other plants (Cohen & Tel-Zur 2012).

This plant is also used as gardening plant known under the name " Princess of the Night" . This is due to its nocturnal flowers which will open for only one night. In June we found that there are 2 groups of clones. In some of the genotypes the anthers will dehisce at around 18.00 and the flowers will start to open 30 minutes later at twilight, when honey bees are still active. They come to drink the nectar which is secreted at the base of the flower. If compatible clones are planted next to each other, pollination is possible at that time. The anther dehiscence of other clones takes place at 19.00, in which flowers will open a few minutes before sunset so the time remaining for bee grazing is very limited and almost no pollination takes place (Weiss et al 1994). After sunrise bees and other day time insects will visit the flowers, however the flower is too big for efficient pollination by these insects (Fig.6). In nature pollination is performed by big insects and even by fruit bats (Silva & Sazima 1995). Today in commercial orchards all flowers are hand pollinated by the growers. The pollen is collected by car vacuum cleaners, mixed with various existing clones and applied by hand with a small brush. This action guarantees over 95% fruit set. Fruit sizes of open pollination from compatible clones grown in close proximity will be 60% of the size of hand pollinated clones (Weiss et al 1994). The flowers are produced throughout the warm season from June to October. One can find flower buds, flowers and fruits of various degrees of development on the shoots at the same time, (Fig.7). We expected columnar cacti to be tolerant to salinity but found them to be severely stressed by 3.5 dS/m of saline water. The picture presented in Fig. 8 was taken in the Arava valley where the main salinity source is Ca, Mg, and sulphates which are less toxic than Na, and Chloride ions. Salinity of 2 dS/m hardly stressed the Koubo and commercial yields were obtained by irrigation at this degree of salinity (Fig.9).

To the best of our knowledge no irrigation and/or fertilization experiments have been performed with this plant. However, since it is a CAM plant the applied irrigation is around 10% of what is used to irrigate C₃ fruit trees, around 100 mm per year (see table 4 in Mizrahi et al 2007). All orchards are drip irrigated and we use fertigation methods, namely with each irrigation we deliver fertilizers of 23/7/23 N/P/K with minor elements. When growers added in each irrigation 70 ppm N of this fertilizer they obtained yields of 20-25 ton/hectare/year. Since so far in Israel we have not found any pests, this crop is commonly grown using organic protocols, with animal manure as fertilizer and covering soil with plastic sheets to avoid the use of weed-killers (Fig. 9).

Propagation.

Since this species is self-incompatible, propagation from seeds is used for breeding, to obtain new genotypes. A lot of work was done by Machado, Mangolin and other coworkers on various techniques for vegetative propagation including mini-propagation ones. (Machado & Prioli 1996, Mangolin et al 2002). However, we found that propagation from cuttings is the easiest and cheapest way. Shoots are cut to 40-50 cm long sections, dried for a week under shade to heal the open wound and then put into any nursery mix to root. Within a few weeks roots are produced and plants are ready to be transferred into the orchard. This will guarantee the establishment of over 97% of plants. Direct planting of cuttings into the orchard is also feasible but the rate of plant establishment is lower ~ 80-85%. We also were able to regenerate whole plants from shoot slices containing a single areole (Fig 10); however, it took 4 more years to achieve full plant production. Today we recommend establishing the 40-50cm long cuttings in pots, and then transfer them into the orchard.

If planting an orchard for hand pollination, one clone can be grown in one separate section of the orchard. Pollen will be collected from the pollinizers section and applied daily from early morning to about 9.00 am. This is to allow efficient pollination when flower is open and the stigma is exposed (Figs 6 & 7). One thousand flowers can be pollinated per hour if a big wave of flowers exists. If pollination by bees and/or other pollinizers is considered, then near each plant, a compatible clone should be planted expecting reduction in fruit sizes of ~ 40% (Weiss et al 1994). We recommend planting 5X2 m distances in the Koubo orchard. Roots are much deeper than the vine-cacti, reaching a depth of 1.5 m. In areas where summer rains prevail, irrigation might be unnecessary.

Tree pruning is performed in winter, to reduce the plant's height to allow easy access to both flowers and fruits, and to open the tree canopy to allow easy access to fruits and flowers and allow light penetration (Fig. 11).

Fruit development, ripening and postharvest behavior.

Fruit start to develop after pollination with compatible pollen. The first stage is a fast growth period (~ 15 days) followed by a slower-rate period (about 10 days) which is then followed by another fast growth period, until full ripening. Fruit reach maximum mass about 45-50 days after anthesis. The first color appears after ~ 35 days while full color is reached at 45-50 days after anthesis. Seeds develop mainly during the second period when growth rate is slowed down. After this stage seeds have a hard black coat and can germinate. At the end of the fruit-development-stage (~ 45-50 days) over 95% of the fruits start to dehisce and crack (Fig. 4). This is a major obstacle for growing various clones for the market. Lack of fruit cracking is an essential characteristic for development of this species. Unfortunately harvesting the fruits in early stages of fruit development leads to un-tasty inedible fruit (Wang 1997). To reach reasonable taste one has to harvest the fruits around full color stage where most clones will crack. The clones we selected can be harvested almost at full color stage and then stored for a few weeks. They should be stored at 10ºC since lower temperatures will induce chilling injury, not only in blackening of the peel but also development of off-flavor. We analyzed fruit composition both immediately after harvest and 2 weeks later after storage at 10ºC. Results are given in Table 1. One should emphasize the following; water content is around 85%, the fruit is rich in fibers (mucilage), and low in sugars. Before ripening the polysaccharide content declines concomitant with rise in soluble sugars. The main sugars are glucose and fructose with traces of sucrose. During ripening, the titratable acidity value decreased by 50% concomitant with the rise in pH. The main acid was malic (~80%), along with Citric, Oxalic and Succinic acids (Wang 1997; Ninio et al 2003a and Ninio et al 2003b). Due to its low sugar content this fruit can possibly be recommended for diabetics. The fruit emits a unique perfume-like odor. Volatiles analysis showed that the main component is linalool and its derivatives. When the fruit is allowed to reach full ripening in storage, the amount of linalool is 17 times higher than in tree-ripe cracked fruit (Ninio et al 2003b). This aroma adds a lot to the acceptance of the fruit by tasters (Wang 1997). We can use the fruit peel color as a reliable ripening index. Before ripening the fruit is green, then changes its color to violet where chlorophyll and betalains red pigments exist together. As the chlorophyll disappears the color is changed to full red in the red clones. The fruit peel stretches and becomes smooth. The best eating quality is reached when the fruit is fully red, however, since fruit cracking appears in most clones, it is recommended to harvest the fruit where some violet still exists and peel is fully stretched. When fruit is stored at 10ºC, shelf-life is over one month which allows the sea-freight to Europe from Israel which is around 10% of the air-freight cost. Reducing the storage temperature to 4ºC, will result in sever chilling injury symptoms such as; peel shriveling and blackening, watery pulp concomitant with off-flavor (Wang 1997).

The fruit is of un-climacteric type but when exposed to ethylene rapid ripening and deterioration will occur (Wang 1997). Hence, it is advisable to ship this fruit in a separate container, not mixed with climacteric fruits.

Marketing of new crop is a major obstacle to the success of establishing sustainable crop (Mizrahi et al 2002). In 2002 a survey was performed by Rut Ela'azar from the Israeli Ministry of Agriculture. She exposed around 100 persons to taste test of koubo fruits. These testers were first time tasters of kuobo and 84% of them claimed that they liked it and were ready to consume it on a regular basis provided the price will be reasonable. Today the fruit is sold for 8-10 Shekels/Kg as a gate-price (1 $US = 3.7 New Israeli Shekels). Fresh fruits are available in the markets from July to January.

Uses other than fresh fruit.

Stems of this species include many kinds of polysaccharides. The arabinogalactan was found to have anti-ulcer properties and can be used for phytotherapy (Tanaka et al 2010). In Israel polysaccharides (mucilage) from fruit and stems are used as a base for various cosmetic products (unpublished and confidential information). Shoot waxes were identified and may be used for various wax needs (Dembitsky & Rezanka 1996; Hughs, et al 1980). We developed several food products from the ripe fruit, among them jam, dry slices of the fruit and excellent aromatic liquor.

CONCLUSIONS

To the best of our knowledge, Israel is the only country which grows this plant as a fruit crop. It has many advantages: a very high water use efficiency- ~ 10 times higher than other C3 fruit tree species, hence, an ideal fruit crop for semi-arid zones; it can tolerate very high temperatures accompanied with very low relative humilities; no pests are known in Israel, hence, an ideal crop to be grown under organic protocols; easy and cheap to propagate from cuttings; only three years to commercial production; can be used to produce various fruit products; long shelf-life suitable to reach the world markets; other products can be made from the stems. In spite of the fact that it is really new crop, with all difficulties involved in marketing, first time consumers were ready to buy it on a permanent basis; it has low sugar content, suitable for diabetic consumers. Special attention should be given to the fact that it can be introduced as a weed. This risk is minimal in semi-arid areas like in Israel. There is still a tremendous amount of knowledge to be accumulated about this crop, since research is still in its infancy.

New Crops and New Uses. ASHS Press, Alexandria,

ACKNOWLEDGEMENT

The author would like to thank Dr. Tali Brunner for editing this manuscript.

Recebido em: 20-09-2013.

Aceito para publicação em: 15-12-2013.

• COHEN, H.; TEL-ZUR, N. Morphological changes and self-incompatibility breakdown associated with autopolyploidization in Hylocereus species (Cactaceae). Euphytica, Wageningen, v.184, n.3, p.345-354, 2012.
• DEMBITSKY,V.M.; REZANKA, T. Molecular species of wax esters in Cereus peruvianus Phytochemistry, New York, v. 42, n.4, p.1075-1080, 1996.
• GUTMAN F.; BAR-ZVI D.; NERD A.; MIZRAHI Y. Molecular typing of Cereus peruvianus clones and their genetic relationship with other Cereus species evaluated by RAPD analysis. Journal of Horticultural Science and Biotechnology, Asford, v.76, p.709-713, 2001.
• HUGHS, J.; RAMOS, G.; MOYNA, P. Main Components in Cereus peruvianus Epicuticular Wax. Journal of Natural Products, Cincinnati, v.43, n.5, p. 564-566, 1980.
• LESHEM, Y.; NERD, A.; MIZRAHI, Y. Fruit cracking in Cereus peruvianus, a new cactus crop. Journal of Horticulture Science and Biotechnology, Asford, v.78. n.3, p.426-431, 2003.
• MACHADO, M.D.P.; PRIOLI, A.J. Micropropagation of Cereus peruvianus Mill (Cactaceae) by areole activation. In Vitro Cellular & Developmental Biology-Plant, Columbia, v.32, n.3, p.199-203, 1996.
• MANGOLIN, C.A.; LAURA M. M.; OTTOBONI, L.M.M.; DE FATIMA, M.; MACHADO M.P.D. RAPD Markers to evaluate callus tissue of Cereus peruvianus Mill. (Cactaceae) maintained in different growth regulator combinations. Biochemical Genetics, New York, v.40. n.(9/10), p.351-358, 2002.
• MIZRAHI, E.; RAVEH, E.; YOSSOV, A.; NERDA .; BEN-ASHER, J. New fruit crops with high water use efficiency. In: JANICK, J.; WHIPKEY, A. (Ed.). Creating markets for economic development of new crops and new uses. Alexandria: ASHS Press, 2007. p.216-222. Disponível em: <http://www.hort.purdue.edu/newcrop/ncnu07/pdfs/mizrahi216-222.pdf>. Acesso em: 11 fev. 2013.
• MIZRAHI, Y.; NERD, A. Climbing and columnar cacti: new arid land fruit crops. In: JANICK, J. (Ed.). Perspectives on new crops and new uses. Alexandria: ASHS Press, 1999. p.358-366.
• MIZRAHI, Y.; NERD, A.; SITRIT, Y. New fruits for arid climates. In: JANICK, J.; WHIPKEY, A. (Ed.). Trends in new crops and new uses. Alexandria: ASHS Press, 2002. p.378-384.
• MORAN, V.C.; ZIMMERMANN, H.G. Biologicalcontrol of cactus weeds of minor importance in South-Africa. Agriculture Ecosystems & Environment, Amsterdam, v.37. n.1-3, p.37-55, 1991.
• NERD, A.; ARONSON, J.A.; MIZRAHI, Y. Introduction and domestication of rare fruits and nut trees for desert areas. In: JANICK, J.; SIMON, J.E. (Ed.). Advances in new crops. Oregon: Timber Press, 1990. p.355-363.
• NERD, A.; RAVEH, E.; MIZRAHI, Y. Adaptation of five columnar cactus species to various conditions in the negev desert of Israel. Economy Botany, Bronx, v.43, n.3, p. 31-41, 1993.
• NERD, A.; MIZ RAHI, Y. Fruit of vine and columnar cacti. In; NOBEL, P.S. Cacti: biology and uses. Berkeley: University of California Press, 2002. p.185-197.
• NEWBIGIN, E.; ANDERSON, M.A.; CLARKE, A.E. Gametophytic self-incompatibility systems. The Plant Cell, Rockville, v.5, p.1315-1324, 1993.
• NINIO, R.; LEWINSOHN, E.; MIZRAHI, Y.; SITRIT, Y. Changes in sugars, acids, and aroma volatiles during ripening of Koubo (Cereus peruvianus (L.) Miller. Journal of Agricultural and Food Chemistry, Easton, v.51, p.797-801, 2003a.
• NINIO, R.; LEWINSOHN, E.; MIZRAHI, Y.; SITRIT, Y. Quality attributes of stored Koubo (Cereus peruvianus (L.) Miller fruit. Postharvest Biology and Technology, Amsterdam, v.30, p.273-280, 2003b.
• OLCKERS, T. Targeting emerging weeds for biological control in South Africa: the benefits of halting the spread of alien plants at an early stage of their invasion. South African Journal of Science, Johannesburg, v.100, n.1, p.64-68, 2004.
• ORTIZ-HERNÁNDEZ, Y. Pitahaya a new crop for México. Mexico:. Limusa Noriega Editors, 1999. (Serie biotecnologias)
• PIMIENTA-BARRIOS, B.E.; NOBEL P.S. Pitaya (Stenocereus spp., Cactaceae) an ancient and modern fruit crop of Mexico. Economic Botany, Bronx, v.48, p.76-83, 1994.
• PIMIENTA-BARRIOS, B.E.; NOBEL P.S. Reproductive characteristics of pitayo (Stenocereus queretaroensis (Weber) Buxbaum) and their relationships with soluble sugars and irrigation. Journal of the American Society for Horticultural Science, Alexandria, v.120, p.1082-1086, 1995.
• PIMIENTA-BARRIOS, B.E.; NOBEL P.S. Vegetative reproductive and Physiological adaptations to aridity of pitayo (Stenocereus queretaroensis, Cactaceae). Economic Botany, Bronx, v.52, p.391-401, 1998a.
• PIMIENTA-BARRIOS, E.; NOBEL, P.S.; ROBLESMURGUIA, C.; MENDEZ-MORAN, L.; YEPEZGONZALEZ, E. Ethnobotany, productivity, and ecophysiology of pitaya (Stenecereus queretaroensis). Journal of the Professional Association for Cactus Development, Chapingo, v.2, p.29-47, 1997.
• PIMIENTA-BARRIOS, E.; HERNÁNDEZ, G.; DOMÍNGUEZ, A.; NOBEL P.S. Growth and development of the columnar cactus Stenocereus queretaroensis (Weber) Buxbaum in a subtropical environment. Tree Physiology, Oxford, v.18, p.459-464, 1998b.
• SILVA, W.R.; SAZIMA, M. Hawk moth Pollination In Cereus peruvianus a Columnar Cactus From Southeastern Brazil. Flora, London, v.190, n.4, p.339-343,1995.
• TANAKA, L.Y.A.; DE OLIVEIRAA, A.J.B.; GONC, J.E.; CIPRIANIC, T.R.; DE SOUZA C, L.M.; MARQUESD, M.C.A.; DE PAULA WERNERD, M.F.; BAGGIOD, C.H.; GORINC, P.A.J.; SASSAKIC, G.L.; LACOMINI, M. An arabinogalactan with anti-ulcer protective effects isolated from Cereus peruvianus Carbohydrate Polymers, Barking, v.82, p.714-721, 2010.
• TEL-ZUR, N.; ABBO, S.; BAR-ZVI, D.; MIZRAHI, Y. Genetic relationships among Hylocereus and Selenicereus Vine Cacti (Cactaceae): evidence from hybridization and cytological studies. Annals of Botany, London, v.93, p.329-333, 2004.
• TEL-ZUR, N.; MIZRAHI, Y.; CISNEROS, A.; MOUYAL, J.; SCHNEIDER, B.; DOYLE, J. J. Phenotypic and genomic characterization of vine cactus collection (Cactaceae). Genetic Resource and Crop Evolution, Dordrecht, v.58, p.1075-1085, 2011.
• WANG, X. Biology of ripening of apple cactus (Cereus peruvianus (L.) Miller). 1997. Thesis (Ph.D) - Ben-Gurion University of the Negev, Beer Sheva, 1997.
• WEISS, J.; NERD, A.; MIZRAHI, Y., Development of Cereus peruvianus (apple cactus) as a new crop for the Negev desert of Israel. In: JANICK, J.; SIMON, J.E. (Ed.). New crops New York: Wiley and Sons, 1993. p.486-491.
• WEISS, J.; NERD, A.; MIZRAHI, Y. Flowering and pollination requirements in Cereus peruvianus cultivated in Israel. Israel Journal of Plant Sciences, Jerusalém, v.42, p.149-158, 1994.

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(Trabalho 447-13).

Palestra II Simpósio Internacional de Fruticultura-Frutas Exóticas, 21 a 25 de outubro de 2013. Jaboticabal-SP.

Publication Dates

• Publication in this collection
  14 Aug 2014
• Date of issue
  Mar 2014

History

• Received
  20 Sept 2013
• Accepted
  15 Dec 2013