Skip to main content
Log in

Sexuality and apogamy in the Cuban Asplenium auritummonodon complex (Aspleniaceae)

  • Original Article
  • Published:
Plant Systematics and Evolution Aims and scope Submit manuscript

Abstract

Asplenium auritum Sw. is a sexual fern that produces 64 spores per sporangium, while A. monodon Liebm. is an apogamous species that produces 32 spores. The hybrid between them, A. × lellingerianum Sánchez & Regalado, also shows an apogamous life cycle, with mainly abortive spores. The scope of this work was to study the sexual and apogamous behavior in these taxa. We studied spore germination and gametophyte development of the three species, a process that followed the Adiantum type. Afterward, we observed morphological apogamous characters in A. monodon and A. × lellingerianum. Apogamous sporophytes arose from apical and basal regions of gametophytes, lacking feet and roots in the first instance, but developing other normal sporophytic structures, such as tracheids, stomata, glandular hairs, and scales. Finally, we studied the gametangia production in all three taxa, finding that the scarce production of antheridia in A. monodon is indicative of the Braithwaite apogamous life cycle scheme, and this scheme has probably been inherited by A. × lellingerianum.

This is a preview of subscription content, log in via an institution to check access.

Access this article

Price excludes VAT (USA)
Tax calculation will be finalised during checkout.

Instant access to the full article PDF.

Fig. 1
Fig. 2
Fig. 3
Fig. 4
Fig. 5
Fig. 6
Fig. 7
Fig. 8

Similar content being viewed by others

References

  • Adams DC (1995) Asplenium. In: Davidse G, Sousa M, Knapp S (eds) Flora Mesoamericana vol. 1, Psilotaceae a Salviniaceae. Universidad Nacional Autónoma de México, México D.F., pp 234–290

    Google Scholar 

  • Atkinson LR, Stokey AG (1964) Comparative morphology of the gametophyte of homosporous ferns. Phytomorphology 14:51–71

    Google Scholar 

  • Barrington DS, Haufler CH, Werth CR (1989) Hybridization, reticulation, and species concepts in the ferns. Am Fern J 79(2):55–64

    Google Scholar 

  • Bell PR, Richards BM (1958) Induced apospory in polypodiaceous ferns. Nature 182:1748–1749

    Article  Google Scholar 

  • Braithwaite AF (1964) A new type of apogamy in ferns. New Phytol 63:293–305

    Article  Google Scholar 

  • Braithwaite AF (1986) The Asplenium aethiopicum complex in South Africa. Bot J Linn Soc 93:343–378

    Article  Google Scholar 

  • Döpp W (1939) Cytologische und genetische Untersuchungen innerhalb der Gattung Dryopteris. Planta 29:481–533

    Article  Google Scholar 

  • Dyer A (1979) The culture of fern gametophytes for experimental investigation. In: Dyer A (ed) The experimental biology of ferns. Academic Press, London, pp 254–305

    Google Scholar 

  • Edwards ME, Miller JH (1972) Growth regulation by ethylene in fern gametophytes III. Inhibition of spore germination. Am J Bot 59:458–465

    Article  CAS  Google Scholar 

  • Evans AM (1969) Interspecific relationships in the Polypodium pectinatumplumula complex. Ann Missouri Bot Gard 55:193–293

    Article  Google Scholar 

  • Farrar DR, Dassler C, Watkins JE, Skelton C (2008) Gametophyte ecology. In: Ranker TA, Haufler CH (eds) The biology and evolution of ferns and lycophytes. Cambridge University Press, Cambridge

    Google Scholar 

  • Gastony GJ, Windham MD (1989) Species concepts in pteridophytes: the treatment and definition of agamosporous species. Am Fern J 79(2):65–77

    Article  Google Scholar 

  • Jarrett FM, Manton I, Roy SK (1968) Cytological and taxonomical notes on a small collection of living ferns from Galapagos. Kew Bull 22:475–480

    Article  Google Scholar 

  • Lovis JD (1973) A biosystematic approach to phylogenetic problems and its application to the Aspleniaceae. Bot J Linn Soc 67:211–228

    Google Scholar 

  • Manton I (1950) Problems of cytology and evolution in the Pteridophyta. Cambridge University Press, Cambridge

    Google Scholar 

  • Mickel JT, Beitel JM (1988) Pteridophyte flora of Oaxaca, Mexico. Mem New York Bot Gard 46:1–568

    Google Scholar 

  • Mickel JT, Smith AR (2004) The pteridophytes of Mexico. Mem New York Bot Gard 88:72–132

    Google Scholar 

  • Morton CV, Lellinger DB (1966) The Polypodiaceae subfamily Asplenioideae in Venezuela. Mem New York Bot Gard 15:1–49

    Google Scholar 

  • Morzenti VM (1966) Morphological and cytological data on southeastern United States species of the Asplenium heterochroumresiliens complex. Am Fern J 56(4):167–177

    Article  Google Scholar 

  • Morzenti VM (1969) Apomixis in ferns with special reference to sterile hybrids. Ph.D. Dissertation, University of Michigan, Michigan

  • Murakami M, Iwatsuki K (1983) Observations on the variation of Asplenium unilaterale in Japan with special reference to apogamy. J Jpn Bot 58(9):257–262

    Google Scholar 

  • Nayar BK, Kaur S (1969) Types of prothallial development in homosporous ferns. Phytomorphology 19:171–188

    Google Scholar 

  • Nayar BK, Kaur S (1971) Gametophytes of homosporous ferns. Bot Rev 37(3):295–396

    Article  Google Scholar 

  • Proctor GR (1977) Flora of Lesser Antilles, Leeward and Windward Islands. Vol 2. Pteridophyta. Arnold Arboretum, Harvard University, Jamaica Plain

    Google Scholar 

  • Proctor GR (1985) Ferns of Jamaica. British Museum (Natural History), London

    Google Scholar 

  • Raghavan V (1989) Developmental biology of fern gametophytes. Cambridge University Press, Cambridge

    Book  Google Scholar 

  • Regalado L, Sánchez C (2001) Problemática del complejo Asplenium auritum Sw. (Aspleniaceae: Pteridophyta) y especies afines en Cuba. Rev Jard Bot Nac Univ Habana 22(1):7–28

    Google Scholar 

  • Regalado L, Sánchez C (2002) Spore morphology as a taxonomic tool in the delimitation of three Asplenium L. species complexes (Aspleniaceae: Pteridophyta) in Cuba. Grana 41:107–113

    Article  Google Scholar 

  • Sánchez C, Regalado L (2003) Aspleniaceae. In: Greuter W (ed) Flora de la República de Cuba, vol 8(1). Taunus, Königstein, pp 3–65

    Google Scholar 

  • Smith AR (1981) Pteridophytes. In: Breedlove DE (ed) Flora of Chiapas; part 2. California Academy of Sciences, San Francisco, pp 1–370

    Google Scholar 

  • Soare LC, Vişoiu E, Andrei M (2007) Researches concerning the in vitro differentiation of the fern Phegopteris connectilis (Michx.) Watt. Notul Bot Hort Agrobot Cluj-Napoca Inst 35(1):7–14

    Google Scholar 

  • Steil WN (1933) New cases of apogamy in certain homosporous leptosporangiate ferns. Bot Gaz 95:164–167

    Article  Google Scholar 

  • Steil WN (1939) Apogamy, apospory, and parthenogenesis in pteridophytes. Bot Rev 5:433–453

    Article  Google Scholar 

  • Steil WN (1951) Apogamy, apospory, and parthenogenesis in pteridophytes II. Bot Rev 17:90–104

    Article  Google Scholar 

  • Stolze RG (1981) Ferns and fern allies of Guatemala II. Polypodiaceae. Fieldiana Bot 6:59–95

    Google Scholar 

  • Stolze RG (1986) Polypodiaceae–Asplenioideae. In: Harling G, Sparre B (eds) Flora de Ecuador. Department of Systematic Botany, University of Göteberg, Göteberg, pp 1–83

    Google Scholar 

  • Tryon AF (1968) Comparison of sexual and apogamous races in the fern genus Pellaea. Rhodora 70:1–24

    Google Scholar 

  • Tryon RM, Stolze RG (1993) Pteridophyta of Peru. Part V. 18. Aspleniaceae–21. Polypodiaceae. Fieldiana Bot 32:1–49

    Google Scholar 

  • Wagner WH (1963) A byosystematic survey of United States ferns—preliminary abstracts. Am Fern J 53(1):1–16

    Article  Google Scholar 

  • Walker TG (1966) A cytotaxonomic survey of the pteridophytes of Jamaica. Trans R Soc Edinburgh 66:169–237

    Google Scholar 

  • Walker TG (1979) The cytogenetics of ferns. In: Dyer AF (ed) The experimental biology of ferns. Academic Press, London, pp 87–132

    Google Scholar 

  • Walker TG (1985) Cytotaxonomic studies of the ferns of Trinidad. 2. The cytology and taxonomic implications. Bull Brit Mus (Nat Hist) Bot 13(2):149–249

    Google Scholar 

  • Whittier DP (1966) Induced apogamy in diploid gametophytes of Pteridium. Can J Bot 44:1717–1721

    Article  Google Scholar 

  • Whittier DP (2004) Induced apogamy in Tmesipteris (Psilotaceae). Can J Bot 82(6):721–725

    Article  Google Scholar 

  • Whittier DP, Steeves TA (1960) The induction of apogamy in the bracken ferns. Can J Bot 38:925–930

    Article  CAS  Google Scholar 

  • Whittier DP, Steeves TA (1962) Further studies on the induction of apogamy in ferns. Can J Bot 40:1525–1531

    Article  CAS  Google Scholar 

Download references

Acknowledgments

Authors are grateful to an anonymous reviewer for the valuable comments and suggestions, which greatly improved the manuscript, and also to William Clarke for the English review. This research was supported by the Agreement of Cooperation between Universidad Complutense de Madrid, Spain, and Agencia de Medio Ambiente, Cuba, which funded two stays for the first author at the Departamento de Biología Vegetal I, Universidad Complutense de Madrid.

Author information

Authors and Affiliations

Authors

Corresponding author

Correspondence to J. M. Gabriel y Galán.

Rights and permissions

Reprints and permissions

About this article

Cite this article

Regalado Gabancho, L., Prada, C. & Gabriel y Galán, J.M. Sexuality and apogamy in the Cuban Asplenium auritummonodon complex (Aspleniaceae). Plant Syst Evol 289, 137–146 (2010). https://doi.org/10.1007/s00606-010-0339-5

Download citation

  • Received:

  • Accepted:

  • Published:

  • Issue Date:

  • DOI: https://doi.org/10.1007/s00606-010-0339-5

Keywords

Navigation