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Reproductive systems and crossing potential in three species ofBulbophyllum (Orchidaceae) occurring in Brazilian ‘campo rupestre’ vegetation

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Abstract

Experimental self-, cross- and interspecific pollinations were carried out inBulbophyllum weddellii, B. involutum andB. ipanemense (Orchidaceae). The last two species are closely related, butB. weddellii is somewhat more distant. The three species are self-compatible, with pollination by a vector necessary for fruit formation. In all crossing types, high rates of fruit abortion and formation of seeds without embryos were observed, particularly in interspecific crosses that involvedB. weddellii. Crosses between the more closely relatedB. involutum andB. ipanemense produced fruit formation rates and seed viability similar to those obtained in intraspecific crosses. These results agree with current hypotheses that suggest that interspecific crossing rates reflect phylogenetic proximity. Examination of pollen tube growth and aborted fruits suggests that a series of factors may be involved in the high abortion rate for fruits and large proportion of seeds without embryos. The low interspecific fertility noted forB. weddellii andB. involutum is important in the maintenance of isolation between these species that are sympatric, flower in the same period and share the same pollinators.

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References

  • Ackerman J. D., Oliver J. C. M. (1985) Reproductive biology ofOncidium variegatum: moon phases, pollination, and fruit set. Amer. Orchid Soc. Bull. 54: 326–329.

    Google Scholar 

  • Agnew J. D. (1986) Self-compatibility/incompatibility in some orchids of the subfamilyVandoideae. Pl. Breed. 97: 183–186.

    Google Scholar 

  • Bertin R. I. (1990) Effects of pollination intensity inCampsis radicans. Amer. J. Bot. 77: 178–187.

    Google Scholar 

  • Borba E. L., Semir J. (1998b)Bulbophyllum xcipoense (Orchidaceae), a new natural hybrid from the Brazilian ‘campos rupestres’: description and biology. Lindleyana: 13: 113–120.

    Google Scholar 

  • Borba E. L., Semir J. (1998a) Wind-assisted fly pollination in threeBulbophyllum (Orchidaceae) species occurring in the Brazilian ‘campos rupestres’. Lindleyana 13: 203–218.

    Google Scholar 

  • Borba E. L., Semir J. (1999) Temporal variation in pollinarium size after its removal in species ofBulbophyllum: a different mechanism preventing self-pollination inOrchidaceae. Plant Syst. Evol. 217: 197–204.

    Google Scholar 

  • Catling P. M. (1982) Breeding systems of northeastern North AmericanSpiranthes (Orchidaceae). Canod. J. Bot. 60: 3017–3039.

    Google Scholar 

  • Christensen D. E. (1992) Notes on the reproductive biology ofStelis argentata Lindl. (Orchidaceae: Pleurothallidinae) in eastern Ecuador. Lindleyana 7: 28–33.

    Google Scholar 

  • Dafni A., Calder D. M. (1987) Pollination by deceit and floral mimesis inThelymitra antennifera (Orchidaceae). Plant Syst. Evol. 158: 11–22.

    Google Scholar 

  • Dressler R. L. (1981) The orchids: natural history and classification. Harvard University Press, Cambridge.

    Google Scholar 

  • Dressler R. L. (1993) Phylogeny and classification of the orchid family. Cambridge University Press, Cambridge.

    Google Scholar 

  • Faulkner J. S. (1973) Experimental hybridization of north-west European species inCarex sectionAcutae (Cyperaceae). Bot. J. Linn. Soc. 67: 233–253.

    Google Scholar 

  • Gonzáles-Dias N., Ackerman J. D. (1988) Pollination, fruit set, and seed production in the orchid,Oeceoclades maculata. Lindleyana 3: 150–155.

    Google Scholar 

  • Hauser T. P., Loeschcke V. (1996) Drought stress and inbreeding depression inLychnis flos-cuculi (Caryophyl-laceae). Evolution 50: 1119–1126.

    Google Scholar 

  • Hogenboom N. G. (1975) Incompatibility and incongruity: two different mechanisms for the non-functioning of intimate partner relationships. Proc. Roy. Soc. London, Ser. B., Biol. Sci. 188: 361–375.

    Google Scholar 

  • Iannotti M. A., Stort M. N. S., Marin-Morales M. A. (1987) O sistema reprodutivo deEpidendrum rigidum Jacq. (Orchidaceae). Ci. & Cult. 39: 641–644.

    Google Scholar 

  • Johansen B. (1990) Incompatibility inDendrobium (Orchidaceae). Bot. J. Linn. Soc. 103: 165–196.

    Google Scholar 

  • Johri B. M., Vasil K. (1961) Physiology of pollen. Bot. Rev. 27: 325–381.

    Google Scholar 

  • Lloyd D. G. (1980) Sexual strategies in plants. I. An hypothesis of serial adjustment of maternal investment during one reproductive session. New Phytol. 86: 69–79.

    Google Scholar 

  • Marshall D. L., Folsom M. W. (1991) Mate choice in plants: an anatomical to population perspective. Ann. Rev. Ecol. Syst. 22: 37–63.

    Google Scholar 

  • Martin F. W. (1959) Staining and observing pollen tubes in the style by means of fluorescence. Stain Technol. 34: 125–128.

    PubMed  Google Scholar 

  • Mehrloff L. A. (1983) Pollination in the genusIsotria (Orchidaceae). Amer. J. Bot. 70: 1444–1453.

    Google Scholar 

  • Nettancourt D. (1977) Incompatibility in angiosperms. Springer, Heidelberg New York Berlin.

    Google Scholar 

  • Niesenbaum R. A., Casper B. B. (1994) Pollen tube numbers and selective fruit maturation inLindera benzoin. Amer. Naturalist 144: 184–191.

    Google Scholar 

  • Pavanelli E. A. S., Stort M. N. S. (1985) Cruzamentos artificiais em plantas deEpidendrum nocturnum Jacq. (Orchidaceae). Ci. & Cult. 37: 1164–1168.

    Google Scholar 

  • Pedersen H. A. (1995) Anthecological observations onDendrochilum longibracteatum — a species pollinated by facultatively anthophilous insects. Lindleyana 10: 19–28.

    Google Scholar 

  • Pijl L. van der, Dodson C. H. (1966) Orchid flowers: their pollination and evolution. University of Miami Press, Coral Gables.

    Google Scholar 

  • Richards A. J. (1986) Plant breeding systems. Allen & Unwin, London.

    Google Scholar 

  • Sanford W. W. (1964) Sexual compatibility relationship inOncidium and related genera. Amer. Orchid Soc. Bull. 33: 1035–1048.

    Google Scholar 

  • Sanford W. W. (1967) Sexual compatibility relationship inOncidium and related genera — part II. Amer. Orchid Soc. Bull. 36: 114–122.

    Google Scholar 

  • Sazima M. (1978) Polinização por moscas emBulbophyllum warmingianum Cogn. (Orchidaceae), na Serra do Cipó, Minas Gerais, Brazil. Revista Brazil. Bot. 1: 133–138.

    Google Scholar 

  • Scacchi R., De Angelis G., Lanzana P. (1990) Allozime variation among and within elevenOrchis species (fam.Orchidaceae), with special reference to hybridization aptitude. Genetica 81: 143–150.

    Google Scholar 

  • Selberg O. (1989) Genome analysis, phylogeny, and classification. Plant Syst. Evol. 166: 159–171.

    Google Scholar 

  • Stephenson A. G. (1981) Flower and fruit abortion: proximate causes and ultimate functions. Annual. Rev. Ecol. Syst. 12: 253–279.

    Google Scholar 

  • Stort M. N. S. (1972) Estudos em híbridos F1 artificiais de orquídeas. Ciên. Cult. 24: 847–851.

    Google Scholar 

  • Stort M. N. S. (1973) Natural pollination inCattleya loddigesii Lindl. Amer. Orchid Soc. Bull. 42: 606–608.

    Google Scholar 

  • Stort M. N. S. (1976) Cruzamentos artificiais entre plantas diplóides e tetraplóides deCattleya bicolor Lindl. Ciên. Cult. 28: 1208–1211.

    Google Scholar 

  • Stort M. N. S. (1982) Cruzamentos artificiais envolvendo espécies do gêneroCattleya, subgênerosMonophyllae eCattleya (Orchidaceae). Ciên. Cult. 35: 1481–1485.

    Google Scholar 

  • Stort M. N. S. (1986) Fertilidade de cruzamentos e relação filogenética entre algumas espécies do gêneroCattleya (Orchidaceae). Revista Brazil. Bot. 9: 69–73.

    Google Scholar 

  • Stort M. N. S., Galdino G. L. (1984) Self and cross-pollination in some species of the genusLaelia Lindl. (Orchidaceae). Revista Brazil. Genet. 7: 671–676.

    Google Scholar 

  • Swamy B. G. L. (1949) Embryological studies in theOrchidaceae. II. Embryogeny. Amer Midland Naturalist 41: 202–232.

    Google Scholar 

  • Tremblay R. L. (1994) Frequency and consequences of multi-parental pollinations ofCypripedium calceolus var.pubescens (Orchidaceae). Lindleyana 9: 161–167.

    Google Scholar 

  • Weiblen G. D., Brehm B. G. (1996) Reproductive strategies and barriers to hybridization betweenTellima grandiflora andTolmeia menziesii (Saxifraceae). Amer. J. Bot. 83: 910–918.

    Google Scholar 

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Authors and Affiliations

  1. Departamento de Botânica, Universidade Estadual de Campinas, Cx. P. 6109, 13083-970, Campinas, São Paulo, Brazil

    Eduardo Leite Borba, George John Shepherd & João Semir

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  1. Eduardo Leite Borba
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  2. George John Shepherd
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  3. João Semir
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Borba, E.L., Shepherd, G.J. & Semir, J. Reproductive systems and crossing potential in three species ofBulbophyllum (Orchidaceae) occurring in Brazilian ‘campo rupestre’ vegetation. Pl Syst Evol 217, 205–214 (1999). https://doi.org/10.1007/BF00984366

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  • DOI: https://doi.org/10.1007/BF00984366

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