دورية أكاديمية
Reproductive biology and pollinators in two enantiostylous Qualea species (Vochysiaceae) in the Brazilian Cerrado.
العنوان: | Reproductive biology and pollinators in two enantiostylous Qualea species (Vochysiaceae) in the Brazilian Cerrado. |
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المؤلفون: | Morais JM; Departament of Botany, Institute of Biological Sciences, University of Brasília, Brasília, DF, Brazil., Consolaro HN; Departament of Biological Sciences, Institute of Biotecnology, Federal University of Catalão, Catalão, GO, Brazil., Bergamini LL; Centro de Estudos Ambientais do Cerrado, IBGE Ecological Reserve, Brasília, DF, Brazil., Ferrero V; Centre for Functional Ecology, Department of Life Sciences, University of Coimbra, Coimbra, Portugal. |
المصدر: | Plant biology (Stuttgart, Germany) [Plant Biol (Stuttg)] 2020 Sep; Vol. 22 (5), pp. 872-880. Date of Electronic Publication: 2020 Jul 04. |
نوع المنشور: | Journal Article |
اللغة: | English |
بيانات الدورية: | Publisher: Wiley Country of Publication: England NLM ID: 101148926 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1438-8677 (Electronic) Linking ISSN: 14358603 NLM ISO Abbreviation: Plant Biol (Stuttg) Subsets: MEDLINE |
أسماء مطبوعة: | Publication: Oxford, England : Wiley Original Publication: Stuttgart : New York, NY : G. Thieme Verlag ; Thieme New York, c1999- |
مواضيع طبية MeSH: | Myrtales*/physiology , Pollination*/physiology, Animals ; Brazil ; Flowers/anatomy & histology ; Pollen ; Reproduction/physiology |
مستخلص: | Enantiostyly is a floral polymorphism in which two floral forms in the same species differ in deflection of the stigma to right or left position. In monomorphic enantiostylous plants, flowers of the two morphs occur within the same individual, usually in the same proportion. In self-compatible species the function of monomorphic enantiostyly is proposed to increase outcrossing rates and offer a reproductive advantage under pollination limitation. Enantiostylous species are usually self-compatible and show heteranthery, with poricide anthers and pollen as pollinator reward; however, there are families, such as Vochysiaceae, that have different characteristics. We analysed the reproductive system and pollination biology of Qualea parviflora and Q. multiflora, two enantiostylous species from the Brazilian Cerrado that have specific morphological and physiological traits. For this, we characterized flower traits, performed hand pollinations and studied floral visitors. We found no differences between morphs in the proportion of flowers, nectar produced or its concentration, pollen quantity and fruit set. Both species were self-incompatible and quite generalist regarding floral visitors. Enantiostyly in self-incompatible plants seems to confer a reproductive advantage by reducing self-interference resulting from stigma clogging. This novel result helps to expand our knowledge on this complex floral polymorphism and opens new avenues for future research on this topic. (© 2020 German Society for Plant Sciences and The Royal Botanical Society of the Netherlands.) |
References: | Allen A.M., Hiscock S.J. (2008) Evolution and phylogeny of self-incompatibility systems in Angiosperms. In: Franklin-Tong V. E. (Ed), Self-incompatibility in flowering plants. Springer, Berlin, Germany, 73-101. de Azevedo I.F.P. (2014) Sistemas reprodutivos em espécies não-arbóreas de fragmento de floresta atlântica do sudeste brasileiro: diversidade, frequência e condições derivadas. Tese Universidade Federal de Viçosa, Viçosa, MG, Brazil. 52f. de Almeida N.M., Castro C.C., Leite A.V.L., Novo R.R., Machado I.C. (2013a) Enantiostyly in Chamaecrista ramosa (Fabaceae, Caesalpinioideae): floral morphology, pollen transfer dynamics and breeding system. Plant Biology, 15, 369-375. de Almeida N.M., Castro C.C., Leite A.V.L., Novo R.R., Machado I.C. (2013b) Floral polymorphism in Chamaecrista flexuosa (Fabaceae, Caesalpinioideae): a possible case of atypical enantiostyly? Annals of Botany, 112, 1117-1123. de Almeida N.M., Bezerra T.T., Oliveira C.R.S., Novo R.R., Siqueira-Filho J.A., Oliveira P.E., Castro C.C. (2015a) Breeding systems of enantiostylous Cassiinae species (Fabaceae, Caesalpinioideae). Flora, 215, 9-15. de Almeida N.M., Cotarelli V.M., Souza D.P., Novo R.R., Siqueira-Filho J.A., Oliveira P.E., Castro C.C. (2015b) Enantiostylous types of Cassiinae species (Fabaceae -Caesalpinioideae). Plant Biology, 17, 740-745. de Jong T.J., Waser N.M., Klinkhamer P.G.L. (1993) Geitonogamy: the neglected side of selfing. Trends in Ecology & Evolution, 8, 321-325. Anderson M.J., Walsh D.C.I. (2013) PERMANOVA, ANOSIM, and the Mantel test in the face of heterogeneous dispersions: What null hypothesis are you testing? Ecological Monographs, 83, 557-574. Antiqueira L.M.O.R., Kageyama P.Y. (2015) Reproductive system and pollen flow in progenies of Qualea grandiflora Mart., a typical species of the Brazilian Cerrado. Revista Árvore, 39, 337-344. Ashman T.-L., Knight T.M., Steets J.A., Amarasekare P., Burd M., Campbell D.R., Dudash M.R., Johnston M.O., Mazer S.J., Mitchell R.J., Morgan M.T., Wilson W.G. (2004) Pollen limitation of plant reproduction: ecological and evolutionary causes and consequences. Ecology, 85, 2408-2421. Aveiro S.M.G. (1997) Biologia da reprodução e crescimento inicial de Qualea cordata Spreng (Vochysiaceae), uma espécie arbórea do Cerrado. Tese Universidade Estadual de Campinas, Campinas, Brazil. 156f. Bahadur B., Kumar P.V., Reddy N.P. (1979) Enantiostyly in Cassia L. (Caesalpinioideae) together with SEM studies of pollen and its possible significance. In Reproduction in flowering plants. Abstr. Int. Symp.. New Zealand, Christchurch,. Barbosa A.A.A. (1983) Aspectos da ecologia reprodutiva de três espécies de Qualea (Vochysiaceae) num Cerrado de Brasília - DF. Dissertação Universidade de Brasília, Departamento de Botânica, Brasília/DF, Brazil. Barrett S.C.H. (2002a) The evolution of plant sexual diversity. Nature Reviews: Genetics, 3, 274-284. Barrett S.C.H. (2002b) Sexual interference of the floral kind. Heredity, 88, 154-159. Barrett S.C.H., Jesson L.K., Baker A.M. (2000) The evolution and function of stylar polymorphisms in flowering plants. Annals of Botany, 85, 253-265. Bates D., Maechler M., Bolker B., Walker S. (2015) Fitting linear mixed-effects models using lme4. Journal of Statistical Software, 67, 1-48. Bohs L., Weese T., Myers N., Lefgren V., Thomas N., van Wagenen A., Stern S. (2007) Zygomorphy and heteranthery in Solanum in a phylogenetic context. Acta Horticulturae, 745, 201-224. Cao G.X., Wu B.X., Xu X.J., Wang X., Yang C.P. (2017) The effects of local variation in light availability on pollinator visitation, pollen and resource limitation of female reproduction in Hosta ventricosa. Botanical Studies, 58, 24. Carmo-Oliveira R., Oliveira P.E., Morretes B.L.D. (2017) Appendicular origin and structure of the spur of Vochysiaceae flowers. Acta Botanica Brasilica, 31, 433-444. Carvalho D.A., Oliveira P.E. (2003) Biologia reprodutiva e polinizacão de Senna sylvestris (Vell.) H.S. Irwin & Barneby (Leguminosae, Caesalpinioideae). Revista Brasileira de Botanica, 26, 319-328. Chao A., Colwell R.K., Lin C., Gotelli N.J. (2009) Sufficient sampling for asymptotic minimum species richness estimators. Ecology, 90, 1125-1133. Custódio L.N., Carmo-Oliveira R., Mendes-Rodrigues C., Oliveira P.E. (2014) Pre-dispersal seed predation and abortion in species of Callisthene and Qualea (Vochysiaceae) in a Neotropical savanna. Acta Botanica Brasilica, 28, 309-320. Fenster C.B. (1995) Mirror image flowers and their effect on outcrossing rate in Chamaecrista fasciculata (Leguminosae). American Journal of Botany, 82, 46-50. Ferrero V., Barrett S.C.H., Rojas D., Arroyo J., Navarro L. (2017) Associations between sex-organ deployment and morph bias in related heterostylous taxa with different stylar polymorphisms. American Journal of Botany, 104, 50-61. Fox J., Weisberg S. (2019) An R companion to applied regression, 3rd edn. Sage, Thousand Oaks CA, USA. Gao J.Y., Ren P.Y., Yang Z.H., Li Q.J. (2006) The pollination ecology of Paraboea rufescens (Gesneriaceae): a buzz-pollinated tropical herb with mirror-image flowers. Annals of Botany, 97, 371-376. Goodwillie C., Kalisz S., Eckert C.G. (2005) The evolutionary enigma of mixed mating: occurrence, theoretical explanations, and empirical evidence. Annual Review of Ecology, Evolution, and Systematics, 36, 47-79. Graham S.W., Barrett S.C.H. (1995) Phylogenetic systematics of Pontederiales. In: Rudall P. J., Cribb P. J., Cutler D. F., Humphries C. J. (Eds), Monocotyledons: systematics and evolution. Royal Botanic Gardens, Kew, UK, pp 415-441. Herbertsson L., Gåvertsson I., Klatt B., Smith H.G. (2017) Assessing the risk of stigma clogging in strawberry flowers due to pollinator sharing with oilseed rape. Journal of Pollination Ecology, 21, 71-77. Holland J.N., Chamberlain A.S. (2007) Ecological and evolutionary mechanisms for low seed:ovule ratios: need for a pluralistic approach? Ecology, 88, 706-715. Hothorn T., Bretz F., Westfall P. (2008) Simultaneous inference in general parametric models. Biometrical Journal, 50, 346-363. Jesson L.K., Barrett S.C.H. (2002) Solving the puzzle of mirror-image flowers. Nature, 417, 707. Jesson L.K., Barrett S.C.H. (2003) The comparative biology of mirror-image flowers. International Journal of Plant Sciences, 164, 237-249. Jesson L.K., Barrett S.C.H. (2005) Experimental tests of the function of mirror-image flowers. Biological Journal of the Linnean Society, 85, 167-179. Jesson L.K., Barrett S.C.H., Day T. (2003) A theoretical investigation of the evolution and maintenance of mirror-image flowers. The American Naturalist, 161, 916-930. Klinkhamer P.G.L., Jong T.J. (1991) Attractiveness to pollinators: a plant’s dilemma. Oikos, 66, 180-184. Knuth P. (1906) Handbook of flower pollination. Clarendon, Oxford, UK. Laporta C. (2005) Floral biology and reproductive system of enantiostylous Senna corymbosa (Caesalpiniaceae) Revista de Biología. Tropical (International Journal of Tropical Biology), 53, 49-61. Leege L.M., Wolfe L.M. (2002) Do floral herbivores respond to variation in flower characteristics in Gelsemium sempervirens (Loganiaceae), a distylous vine? American Journal of Botany, 89, 1270-1274. Leite A.V., Machado I.C. (2010) Reproductive biology of woody species in Caatinga, a dry forest of northeastern Brazil. Journal of Arid Environments, 74, 1374-1380. Lenth R.V. (2016) Least-squares means: the R package lsmeans. Journal of Statistical Software, 69, 1-33. Lloyd D.G. (1992) Self- and cross-fertilization in plants. II. The selection of self-fertilization. International Journal of Plant Science, 153, 370-80. Lloyd D.G., Schoen D.J. (1992) Self- and cross-fertilization in plants. I. Functional dimensions. International Journal of Plant Sciences, 153, 358-369. Lloyd D.G., Webb C.J. (1992) The evolution of heterostyly. In: Barrett S. C. H. (Ed), Evolution and function of heterostyly. Springer, Berlin, Germany, pp 151-178. Mora-Carrera E., Castañeda-Zárate M., Fornoni J., Boege K., Domínguez C.A. (2019) On the adaptive value of monomorphic versus dimorphic enantiostyly in Solanum rostratum. Annals of Botany, 123, 205-212. Morais J.M., Consolaro H.N., Bergamini L.L., Ferrero V. (2020). Patterns of pollen flow in monomorphic enantiostylous species: the importance of floral morphology and pollinators___ size. Plant Systematics and Evolution, 306, 22. https://doi.org/10.1007/s00606-020-01627-1. Myers N., Mittermeier R.A., Mittermeier C.G., Fonseca G.A.B., Kent J. (2000) Biodiversity hotspots for conservation priorities. Nature, 403, 853-858. Oksanen J. et al (2018) vegan: community ecology package. R package version 2.5-2. https://CRAN.R-project.org/package=vegan. Oliveira P.E. (1998) Reproductive biology, evolution and taxonomy of the Vochysiaceae in the Central Brazil. In: Owens S. J., Rudall P. J. (Eds), Reproductive biology in sytematics, conservation and economic botany. Royal Botanic Gardens, Kew, UK, pp 381-393. Oliveira P.E., Gibbs P.E., Barbosa A.A. (2004) Moth pollination of woody species in the Cerrados of Central Brazil: a case of so much owed to so few? Plant Systematics and Evolution, 245, 41-54. Palmer M., Travis J., Antonovics J. (1989) Temporal mechanisms influencing gender expression and pollen flow within a self-incompatible perennial, Amianthium muscaetoxicum (Liliaceae). Oecologia, 78, 231-236. Piper J. (1986) The evolution of distyly in Primula vulgaris. Biological Journal of the Linnean Society, 29, 123-137. R Core Team. (2018) R: a language and environment for statistical computing. R Foundation for Statistical Computing, Vienna, Austria. https://www.R-project.org/. Radford A.E., Dickison W.C., Massey J.R., Bell C.R. (1974) Vascular plant systematics. Harper and Row, New York, USA. 891 p. Ratter J.A., Bridgewater S., Ribeiro J.F. (2003) Analysis of the floristic composition of the Brazilian Cerrado Vegetation III: comparison of the woody vegetation of 376 areas. Edinburgh Journal of Botany, 60, 57-109. Rodríguez L., Sanoja E. (2008) Fenología, biología floral de polinización de especies de la familia Vochysiaceae en la Guayana Venezolana. Acta Botanica Venezuelana, 31, 331-366. Santos M.L. (1997) Biologia floral de duas espécies de Vochysiaceae em um Cerrado sobre afloramento basáltico em Araguari, MG. Dissertação Universidade de Brasília, Departamento de Botânica, Brasília/DF, Brazil. 93f. Shimizu G.H. (2016) Phylogenetic, taxonomic and nomenclatural studies in Vochysiaceae and synopsis of Vochysia in Brazil. Tese Universidade de Campinas, Instituto de Biologia, Campinas/SP, Brazil. 126f. Silva Júnior M.C. (2012) 100 Árvores do Cerrado - Sentido restrito: Guia de campo. Brasília, Ed. Rede de sementes do Cerrado. pp. 160-165. Soares S.M.N.A., Kaehler T.G., Araujo R.B., Falconer D., Silva D.P., Monteiro V.M. (2012) Biologia floral, enantiostyly, sistema reprodutivo e potenciais polinizadores de Callisthene minor Mart (Vochysiaceae), Chapada dos Veadeiros - Brazil. Biologia e Ecologia da polinização. Curso de campo, 3, 89-97. Solís-Montero L., Vallejo-Marín M. (2017) Does the morphological fit between flowers and pollinators affect pollen deposition? An experimental test in a buzz-pollinated species with anther dimorphism. Ecology and Evolution, 7, 2706-2715. Vallejo-Marín M., Da Silva E.M., Sargent R.D., Barrett S.C.H. (2010) Trait correlates and functional significance of heteranthery in flowering plants. New Phytologist, 188, 418-425. Wang G., Yamasue Y., Itoha K., Kusanagi T. (1998) Outcrossing rates as affected by pollinators and the heterozygote advantage of Monochoria korsakowii. Aquatic Botany, 62, 135-143. Webb C.J., Lloyd D.C. (1986) The avoidance of interference between the presentation of pollen and stigmas in Angiosperms II. Hercogamy. New Zealand Journal of Botany, 24, 163-178. Westerkamp C. (2004) Ricochet pollination in cassias - and how bees explain enantiostyly. In: Freitas B. M., Pereira J. O. P. (Eds), Solitary bees: conservation, rearing and management for pollination. Imprensa Universitária, Fortaleza, Brazil, pp 225-230. Wickham H. (2016) ggplot2: elegant graphics for data analysis. Springer, New York, USA. Wolowski M., Freitas L. (2010) Breeding system and pollination of Senna multijuga (Fabaceae) in a montane Atlantic Forest. Rodriguésia, 61, 167-179. |
معلومات مُعتمدة: | SFRH/BPD/108707/2015 Portuguese Foundation for Science and Technology (FCT); 2016 Percy Sladen Memorial Fund |
فهرسة مساهمة: | Keywords: Breeding system; Qualea multiflora; Qualea parviflora; floral dimorphism; mirror-image flowers |
تواريخ الأحداث: | Date Created: 20200128 Date Completed: 20210113 Latest Revision: 20210113 |
رمز التحديث: | 20221213 |
DOI: | 10.1111/plb.13091 |
PMID: | 31984595 |
قاعدة البيانات: | MEDLINE |
تدمد: | 1438-8677 |
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DOI: | 10.1111/plb.13091 |