Apomictic fern fathers: an experimental approach to the reproductive characteristics of sexual, apomict, and hybrid fern gametophytes
Jazyk angličtina Země Spojené státy americké Médium print-electronic
Typ dokumentu časopisecké články, práce podpořená grantem
PubMed
35072270
DOI
10.1002/ajb2.1817
Knihovny.cz E-zdroje
- Klíčová slova
- Dryopteris, agamospory, antheridia, apo-sex hybrid, apogamy, archegonia, gametes, hybridization, pteridophytes, wood fern,
- MeSH
- apomixie * genetika MeSH
- kapradiny * genetika MeSH
- lidé MeSH
- otcové MeSH
- rozmnožování MeSH
- zárodečné buňky rostlin MeSH
- Check Tag
- lidé MeSH
- mužské pohlaví MeSH
- Publikační typ
- časopisecké články MeSH
- práce podpořená grantem MeSH
PREMISE: Apomixis and hybridization are two essential and complementary factors in the evolution of plants, including ferns. Hybridization combines characteristics from different species, while apomixis conserves features within a lineage. When combined, these two processes result in apo-sex hybrids. The conditions leading to the formation of these hybrids are poorly understood in ferns. METHODS: We cultivated spores from 66 fern samples (43 apomicts, 7 apo-sex hybrids, and 16 sexuals), and measured their development in vitro over 16 weeks. We evaluated germination, lateral meristem formation rates, sexual expression, and production of sporophytes and then compared ontogenetic patterns among the three groups. RESULTS: The three examined groups formed antheridia (male gametangia) but differed in overall gametophyte development. Sexual species created archegonia (female, 86% of viable samples), but no sporophytes. Apomicts rarely created nonfunctional archegonia (8%) but usually produced apogamous sporophytes (75%). Surprisingly, apomictic and sexual species showed similar development speed. The sexually reproducing parents of viable studied hybrids formed about twice as many meristic gametophytes as the apomictic parents (39% vs. 20%, respectively). CONCLUSIONS: We present the most thorough comparison of gametangial development of sexual and apomictic ferns, to date. Despite expectations, apomictic reproduction might not lead to earlier sporophyte formation. Apomicts produce functional sperm and thus can contribute this type of gamete to their hybrids. The development patterns found in the parents of hybrids indicate a possible increase of hybridization rates by antheridiogens. The apo-sex hybrids always inherit the apomictic reproductive strategy and are thus capable of self-perpetuation.
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Albertini, E., G. Barcaccia, J. G. Carman, and F. Pupilli. 2019. Did apomixis evolve from sex or was it the other way around? Journal of Experimental Botany 70: 2951-2964.
Atallah, N. M., and J. A. Banks. 2015. Reproduction and the pheromonal regulation of sex type in fern gametophytes. Frontiers in Plant Science 6: 100.
Baack, E., M. C. Melo, L. H. Rieseberg, and D. Ortiz-Barrientos. 2015. The origins of reproductive isolation in plants. New Phytologist 207: 968-984.
Bates, D., M. Mächler, B. Bolker, and S. Walker. 2015. Fitting linear mixed-effects models using lme4. Journal of Statistical Software 67: 1-48.
Beri, A., and S. S. Bir. 1993. Germination of stored spores of Pteris vittata L. American Fern Journal 83: 73-78.
ter Braak, C., and P. Šmilauer. 2012. Canoco reference manual and 'user's guide: software of ordination (version 5.0). Microcomputer Power (Ithaca, NY, USA).
Braithwaite, A. F. 1964. A new type of apogamy in ferns. New Phytologist 63: 293-305.
Caetano, A. P. S., S. P. Teixeira, E. R. Forni-Martins, and S. M. Carmello-Guerreiro. 2013. Pollen insights into apomictic and sexual Miconia (Miconieae, Melastomataceae). International Journal of Plant Sciences 174: 760-768.
Carman, J. G., M. Mateo de Arias, L. Gao, X. Zhao, B. M. Kowallis, D. A. Sherwood, M. K. Srivastava, et al. 2019. Apospory and diplospory in diploid Boechera (Brassicaceae) may facilitate speciation by recombination-driven apomixis-to-sex reversals. Frontiers in Plant Science 10: 724.
Chen, Z. J. 2010. Molecular mechanisms of polyploidy and hybrid vigor. Trends in Plant Science 15: 57-71.
Chiou, W.-L., Y.-M. Huang, T.-H. Hsieh, and S.-Y. Hsu. 2006. Diplazium megaphyllum (Bak.) Christ, a rare fern in Taiwan, reproduces by apogamy. Taiwan Journal of Forest Science 21: 39-47.
Chrtek, J., P. Mráz, A. Belyayev, L. Paštová, V. Mrázová, P. Caklová, J. Josefiová, et al. 2020. Evolutionary history and genetic diversity of apomictic allopolyploids in Hieracium s.str.: morphological versus genomic features. American Journal of Botany 107: 66-90.
DeSoto, L., L. G. Quintanilla, and M. Méndez. 2008. Environmental sex determination in ferns: effects of nutrient availability and individual density in Woodwardia radicans. Journal of Ecology 96: 1319-1327.
Doležal, J., A. Krahulcová, T. Urfus, and F. Krahulec. 2020. Residual sexuality of the apomict Pilosella rubra under natural conditions in the Krkonoše Mts. Preslia 92: 403-428.
Döpp, W. 1932. Die Apogamie bei Aspidium remotum Al. Br. 17: 86-152.
Döpp, W. 1950. Eine die Antheridienbildung bei Farnen fördernde Substanz in den Prothallien von Pteridium aquilinum (L.) Kuhn. Berichte der Deutschen Botanischen Gesellschaft 63: 139-147.
Döpp, W. 1959. Über eine hemmende und eine fördernde Substanz bei der Antheridienbildung in den Prothallien von Pteridium aquilinum. Berichte der Deutschen Botanischen Gesellschaft 72: 11-24.
Dubey, J. P., and S. K. Roy. 1985. A new antheridiogen from the fern Pityrogramma calomelanos (L.) Link. Proceedings of the Indian National Science Academy 95: 173-179.
Duncan, R. E. 1943. Origin and development of embryos in certain apogamous forms of Dryopteris. Botanical Gazette 105: 202-211.
Dyer, R. J., V. Savolainen, and H. Schneider. 2012. Apomixis and reticulate evolution in the Asplenium monanthes fern complex. Annals of Botany 110: 1515-1529.
Ekrt, L., and P. Koutecký. 2016. Between sexual and apomictic: unexpectedly variable sporogenesis and production of viable polyhaploids in the pentaploid fern of the Dryopteris affinis agg. (Dryopteridaceae). Annals of Botany 117: 97-106.
Eschelmüller, A. 1998. Keimversuche mit Sporen der triploiden Sipplen von Dryopteris affinis und ihren Bastarden mit Dryopteris filix-mas. Mitteilungen des Naturwisssenschaftlichen Arbeitskreises Kempten 36: 47-78.
Evans, A. M. 1964. Ameiotic alternation of generations: A new life cycle in the ferns. Science 143: 261-263.
Fiaz, S., X. Wang, A. Younas, B. Alharthi, A. Riaz, and H. Ali. 2021. Apomixis and strategies to induce apomixis to preserve hybrid vigor for multiple generations. GM Crops & Food 12: 57-70.
Fraser-Jenkins, C. R. 2007. The species and subspecies in the Dryopteris affinis group. Fern Gazette 18: 1-26.
Gemmrich, A. R. 1986. Antheridiogenesis in the fern Pteris vittata II) hormonal control of antheridium formation. Journal of Plant Physiology 125: 157-166.
Goulet, B. E., F. Roda, and R. Hopkins. 2017. Hybridization in plants: Old ideas, new techniques. Plant Physiology 173: 65-78.
Grusz, A. L. 2016. A current perspective on apomixis in ferns. Journal of Systematics and Evolution 54: 656-665.
Grusz, A. L., M. D. Windham, and K. M. Pryer. 2009. Deciphering the origins of apomictic polyploids in the Cheilanthes yavapensis complex (Pteridaceae). American Journal of Botany 96: 1636-1645.
Grusz, A. L., M. D. Windham, K. T. Picard, K. M. Pryer, E. Schuettpelz, and C. H. Haufler. 2021. A drought-driven model for the evolution of obligate apomixis in ferns: evidence from pellaeids (Pteridaceae). American Journal of Botany 108: 263-283.
Guo, Z.-Y., and H.-M. Liu. 2013. Gametophyte morphology and development of three species of Cyrtogonellum Ching (Dryopteridaceae). American Fern Journal 103: 153-165.
Hajrudinović, A., S. Siljak-Yakovlev, S. C. Brown, F. Pustahija, M. Bourge, D. Ballian, and F. Bogunić. 2015. When sexual meets apomict: genome size, ploidy level and reproductive mode variation of Sorbus aria s.l. and S. austriaca (Rosaceae) in Bosnia and Herzegovina. Annals of Botany 116: 301-312.
Haufler, C. H., and G. J. Gastony. 1978. Antheridiogen and the breeding system in the fern genus Bommeria. Canadian Journal of Botany 56: 1594-1601.
Haufler, C. H., and C. B. Welling. 1994. Antheridiogen, dark spore germination, and outcrossing mechanisms in Bommeria (Adiantaceae). American Journal of Botany 81: 616-621.
Haufler, C. H., K. M. Pryer, E. Schuettpelz, E. B. Sessa, D. R. Farrar, R. Moran, J. J. Schneller, et al. 2016. Sex and the single gametophyte: revising the homosporous vascular plant life cycle in light of contemporary research. BioScience 66: 928-937.
Hernández, M. A., A. R. Andrada, V. de los A. Páez, and O. G. Martínez. 2015. Ploidy level and obligate apogamy in two populations of Argyrochosma nivea var. tenera (Pteridaceae). Hoehnea 42: 233-237.
Hörandl, E. 2010. The evolution of self-fertility in apomictic plants. Sexual Plant Reproduction 23: 73-86.
Hori, K., and N. Murakami. 2019. Origin of the Diplazium hachijoense complex (Athyriaceae). PhytoKeys 124: 57-76.
Hori, K., A. Tono, K. Fujimoto, J. Kato, A. Ebihara, Y. Watano, and N. Murakami. 2014. Reticulate evolution in the apogamous Dryopteris varia complex (Dryopteridaceae, subg. Erythrovariae, sect. Variae) and its related sexual species in Japan. Journal of Plant Research 127: 661-684.
Hori, K., Y. Watano, and N. Murakami. 2016. Hybrid origin of the apogamous fern Dryopteris hondoensis (Dryopteridaceae). Acta Phytotaxonomica et Geobotanica 67: 133-146.
Hori, K., X. Zhou, Y.-H. Yan, Y. Inoue, and N. Murakami. 2018. Evidence for maternal ability in hybridization of apogamous fern species: Dryopteris tsushimense K. Hori & N. Murak. and D. subtsushimense K. Hori & N. Murak. (Dryopteridaceae), new tetraploid apogamous pteridophytes of hybrid origin from Tsushima, Japan. Acta Phytotaxonomica et Geobotanica 69: 143-160.
Hornych, O., and L. Ekrt. 2017. Spore abortion index (SAI) as a promising tool of evaluation of spore fitness in ferns: an insight into sexual and apomictic species. Plant Systematics and Evolution 303: 497-507.
Hornych, O., L. Ekrt, F. Riedel, P. Koutecký, and J. Košnar. 2019. Asymmetric hybridization in Central European populations of the Dryopteris carthusiana group. American Journal of Botany 106: 1477-1486.
Hornych, O., W. L. Testo, E. B. Sessa, J. E. Watkins, C. E. Campany, J. Pittermann, and L. Ekrt. 2021. Insights into the evolutionary history and widespread occurrence of antheridiogen systems in ferns. New Phytologist 229: 607-619.
Huang, Y.-M., H.-M. Chiou, and W.-L. Chiou. 2004. Density affects gametophyte growth and sexual expression of Osmunda cinnamomea (Osmundaceae: Pteridophyta). Annals of Botany 94: 229-232.
Huang, Y.-M., H.-M. Chou, T.-H. Hsieh, J.-C. Wang, and W.-L. Chiou. 2006. Cryptic characteristics distinguish diploid and triploid varieties of Pteris fauriei (Pteridaceae). Canadian Journal of Botany 84: 261-268.
Huang, Y.-M., S.-Y. Hsu, M. H. Huang, and W.-L. Chiou. 2009. Reproductive biology of three Cheilanthoid ferns in Taiwan. The International Journal of Plant Reproductive Biology 1: 109-116.
Huang, Y.-M., S.-Y. Hsu, T.-H. Hsieh, and H.-M. Chou. 2011. Three Pteris species (Pteridaceae: Pteridophyta) reproduce by apogamy. Botanical Studies 52: 79-87.
Jaruwattanaphan, T., S. Matsumoto, and Y. Watano. 2013. Reconstructing hybrid speciation events in the Pteris cretica group (Pteridaceae) in Japan and adjacent regions. Systematic Botany 38: 15-27.
Kentner, E. K., and M. R. Mesler. 2000. Evidence for natural selection in a fern hybrid zone. American Journal of Botany 87: 1168-1174.
Korpelainen, H. 1994. Growth, sex determination and reproduction of Dryopteris filix-mas (L.) Schott gametophytes under varying nutritional conditions. Botanical Journal of the Linnean Society 114: 357-366.
Koutecký, P., T. Baďurová, M. Štech, J. Košnar, and J. Karásek. 2011. Hybridization between diploid Centaurea pseudophrygia and tetraploid C. jacea (Asteraceae): the role of mixed pollination, unreduced gametes, and mentor effects. Biological Journal of the Linnean Society 104: 93-106.
Krahulcová, A., S. Papoušková, and F. Krahulec. 2004. Reproduction mode in the allopolyploid facultatively apomictic hawkweed Hieracium rubrum (Asteraceae, H. subgen. Pilosella). Hereditas 141: 19-30.
Krahulcová, A., O. Rotreklová, and F. Krahulec. 2014. The detection, rate and manifestation of residual sexuality in apomictic populations of Pilosella (Asteraceae, Lactuceae). Folia Geobotanica 49: 239-258.
Laird, S., and E. Sheffield. 1986. Antheridia and archegonia of the apogamous fern Pteris cretica. Annals of Botany 57: 139-143.
Lepší, M., P. Koutecký, J. Nosková, P. Lepší, T. Urfus, and T. C. G. Rich. 2019. Versatility of reproductive modes and ploidy level interactions in Sorbus s.l. (Malinae, Rosaceae). Botanical Journal of the Linnean Society 191: 502-522.
Lin, S.-J., M. Kato, and K. Iwatsuki. 1992. Diploid and triploid offspring of triploid agamosporous fern Dryopteris pacifica. Botanical Magazine Tokyo 105: 443-452.
Liu, H.-M., R. J. Dyer, Z.-Y. Guo, Z. Meng, J.-H. Li, and H. Schneider. 2012. The evolutionary dynamics of apomixis in ferns: A case study from Polystichoid ferns. Journal of Botany 2012: 1-11.
Lloyd, R. M., and E. J. Klekowski. 1970. Spore germination and viability in Pteridophyta: Evolutionary significance of chlorophyllous spores. Biotropica 2: 129-137.
Ma, Y., W. Xie, X. Tian, W. Sun, Z. Wu, and R. Milne. 2014. Unidirectional hybridization and reproductive barriers between two heterostylous primrose species in north-west Yunnan, China. Annals of Botany 113: 763-775.
Manton, I. 1950. Problems of cytology and evolution in the Pteridophyta. Cambridge University Press, London.
Manton, I., S. K. Roy, and F. M. Jarrett. 1966. The cytotaxonomy of some members of the Cheilanthes farinosa complex in Africa and India. Kew Bulletin 18: 553-565.
Martínez, O. G., M. A. Hernández, and M. Ponce. 2017. Reproductive expression of cheilanthoid ferns (Pteridaceae) from South America. Flora 236-237: 126-131.
Mogie, M. 1992. The evolution of asexual reproduction in plants. Springer Netherlands.
Momose, S. 1967. Prothallia of the Japanese ferns (Filicales). University of Tokyo Press, Tokyo.
Murashige, T., and F. Skoog. 1962. A revised medium for rapid growth and bio assays with Tabacco tissue cultures. Physiologia Plantarum 15: 473-497.
Näf, U. 1958. On the physiology of antheridium formation in the Bracken fern [Pteridium aquilinum (L) Kuhn]. Physiologia Plantarum 11: 728-746.
Näf, U. 1966. On dark-germination and antheridium formation in Anemia phyllitidis. Physiologia Plantarum 19: 1079-1088.
Näf, U., K. Nakanishi, and M. Endo. 1975. On the physiology and chemistry of fern antheridiogens. Botanical Review 41: 315-359.
Pangua, E., S. Pajarón, and L. G. Quintanilla. 2019. Fitness of an allopolyploid rupicolous fern compared with its diploid progenitors: from sporogenesis to sporophyte formation. American Journal of Botany 106: 984-995.
Park, C.-H., and M. Kato. 2003. Apomixis in the interspecific triploid hybrid fern Cornopteris christenseniana (Woodsiaceae). Journal of Plant Research 116: 93-103.
Patel, N., C.-X. Li, L.-B. Zhang, and D. S. Barrington. 2018. Biodiversity and apomixis: Insights from the East-Asian holly ferns in Polystichum section Xiphopolystichum. Molecular Phylogenetics and Evolution 127: 345-355.
Podio, M., L. A. Siena, D. Hojsgaard, J. Stein, C. L. Quarin, and J. P. A. Ortiz. 2012. Evaluation of meiotic abnormalities and pollen viability in aposporous and sexual tetraploid Paspalum notatum (Poaceae). Plant Systematics and Evolution 298: 1625-1633.
Poelt, J. 1960. Dryopteris borreri in Bavaria. American Fern Journal 50: 114-117.
Quintanilla, L. G., and A. Escudero. 2006. Spore fitness components do not differ between diploid and allotetraploid species of Dryopteris (Dryopteridaceae). Annals of Botany 98: 609-618.
Quintanilla, L. G., L. DeSoto, A. Jimenez, and M. Mendez. 2007. Do antheridiogens act via gametophyte size? A study of Woodwardia radicans (Blechnaceae). American Journal of Botany 94: 986-990.
R Development Core Team. 2020. R: A language and environment for statistical computing. R Foundation for Statistical Computing, Vienna, Austria.
Regalado Gabancho, L., C. Prada, and J. M. Gabriel y Galán. 2010. Sexuality and apogamy in the Cuban Asplenium auritum-monodon complex (Aspleniaceae). Plant Systematics and Evolution 289: 137-146.
Reyes Jaramillo, I., S. L. Camargo Ricalde, and M. de los Á. Aquiahuatl Ramos. 2008. Mycorrhizal-like interaction between gametophytes and young sporophytes of the fern Dryopteris muenchii (Filicales) and its fungal endophyte. Revista de Biología Tropical 56: 1101-1107.
Rieseberg, L. H., and S. E. Carney. 1998. Plant hybridization. New Phytologist 140: 599-624.
Rotreklová, O., and A. Krahulcová. 2016. Estimating paternal efficiency in an agamic polyploid complex: pollen stainability and variation in pollen size related to reproduction mode, ploidy level and hybridogenous origin in Pilosella (Asteraceae). Folia Geobotanica 51: 175-186.
Sareen, B., A. Bhattacharya, M. Sharma, A. Sood, and P. S. Ahuja. 2014. A simple technique for tracking individual spore and gametophyte development in Adiantum lunulatum Burm. f. using modified extra thin alginate film technique. Indian Journal of Experimental Biology 52: 5.
Šarhanová, P., T. F. Sharbel, M. Sochor, R. J. Vašut, M. Dančák, and B. Trávníček. 2017. Hybridization drives evolution of apomicts in Rubus subgenus Rubus: evidence from microsatellite markers. Annals of Botany 120: 317-328.
Scheben, A., and D. Hojsgaard. 2020. Can we use gene-editing to induce apomixis in sexual plants? Genes 11: 781.
Schedlbauer, M. D., and E. J. Klekowski. 1972. Antheridogen activity in the fern Ceratopteris thalictroides (L.) Brongn. Botanical Journal of the Linnean Society 65: 399-413.
Schneller, J. J. 1981. Bemerkungen zur Biologie der Wurmfarngruppe. Farnblätter 7: 9-17.
Schneller, J. J. 1988. Spore bank, dark germination and gender determination in Athyrium and Dryopteris: results and implications for population biology of Pteridophyta. Botanica Helvetica 98: 77-86.
Schneller, J. J. 2008. Antheridiogens. In T. A. Ranker, and C. H. Haufler [eds.], Biology and evolution of ferns and lycophytes., 134-158. Cambridge University Press, Cambridge, UK.
Sessa, E. B., W. L. Testo, and J. E. Watkins. 2016. On the widespread capacity for, and functional significance of, extreme inbreeding in ferns. New Phytologist 211: 1108-1119.
Sigel, E. M. 2016. Genetic and genomic aspects of hybridization in ferns. Journal of Systematics and Evolution 54: 638-655.
Sigel, E. M., M. D. Windham, L. Huiet, G. Yatskievych, and K. M. Pryer. 2011. Species relationships and farina evolution in the cheilanthoid fern genus Argyrochosma (Pteridaceae). Systematic Botany 36: 554-564.
Smith, D. L., and P. M. Robinson. 1975. The effects of spore age on germination and gametophyte development in Polypodium vulgare L. New Phytologist 74: 101-108.
Steil, W. N. 1918. Studies of some new cases of apogamy in ferns. Bulletin of the Torrey Botanical Club 45: 93-108.
Tanaka, J., K. Yano, K. Aya, K. Hirano, S. Takehara, E. Koketsu, R. L. Ordonio, et al. 2014. Antheridiogen determines sex in ferns via a spatiotemporally split gibberellin synthesis pathway. Science 346: 469-473.
Testo, W. L., M. S. Grasso, and D. S. Barrington. 2014. Beyond antheridiogens: chemical competition between gametophytes of Polypodium appalachianum and Polypodium virginianum. The Journal of the Torrey Botanical Society 141: 302-312.
Testo, W. L., J. E. Watkins, and D. S. Barrington. 2015. Dynamics of asymmetrical hybridization in North American wood ferns: reconciling patterns of inheritance with gametophyte reproductive biology. New Phytologist 206: 785-795.
Tucker, M. R., A.-C. G. Araujo, N. A. Paech, V. Hecht, E. D. L. Schmidt, J.-B. Rossell, S. C. de Vries, and A. M. G. Koltunow. 2003. Sexual and apomictic reproduction in Hieracium subgenus Pilosella are closely interrelated developmental pathways. The Plant Cell 15: 1524-1537.
Tucker, M. R., and A. M. G. Koltunow. 2009. Sexual and asexual (apomictic) seed development in flowering plants: molecular, morphological and evolutionary relationships. Functional Plant Biology 36: 490-504.
Verma, S. C. 1977. Cytology and reproduction of Cheilanthes farinosa from Yemen. Fern Gazette 11: 325-328.
Voeller, B. R. 1964. Antheridiogens in ferns. Regulateurs naturels de la croissance vegetale., 665-684. Gif s/Yvette, Paris.
Wagner, W. H., and K. L. Chen. 1965. Abortion of spores and sporangia as a tool in the detection of Dryopteris hybrids. American Fern Journal 55: 9-29.
Walker, T. G. 1958. Hybridization in some species of Pteris L. Evolution 12: 82-92.
Walker, T. G. 1962. Cytology and evolution in the fern genus Pteris L. Evolution 16: 27-43.
Walker, T. G. 1985. Some aspects of agamospory in ferns-the Braithwaite system. Proceedings of the Royal Society of Edinburgh 86: 59-66.
Whittier, D. P. 1968. “Rate of gametophyte maturation in sexual and apogamous forms of Pellaea glabella.” American Fern Journal 58: 12-19.
Whittier, D. P. 1970. The rate of gametophyte maturation in sexual and apogamous species of ferns. Phytomorphology 20: 30-35.
Whitton, J., C. J. Sears, E. J. Baack, and S. P. Otto. 2008. The dynamic nature of apomixis in the angiosperms. International Journal of Plant Sciences 169: 169-182.
Windham, M. D. 1983. The ferns of Elden Mountain, Arizona. American Fern Journal 73: 85.
Windham, M. D., P. G. Wolf, and T. A. Ranker. 1986. Factors affecting prolonged spore viability in herbarium collections of three species of Pellaea. American Fern Journal 76: 141-148.
Xiang, L., C. R. Werth, S. N. Emery, and D. E. McCauley. 2000. Population-specific gender-biased hybridization between Dryopteris intermedia and D. carthusiana: evidence from chloroplast DNA. American Journal of Botany 87: 1175-1180.
Yatskievych, G. 1993. Antheridiogen response in Phanerophlebia and related rern genera. American Fern Journal 83: 30-36.
Zanella, C. M., C. Palma-Silva, M. Goetze, and F. Bered. 2016. Hybridization between two sister species of Bromeliaceae: Vriesea carinata and V. incurvata. Botanical Journal of the Linnean Society 181: 491-504.