Pollination ecology in Centrosema brasilianum (L.) Benth. (Fabaceae: Papilionoideae): bee size influences pollen deposition
DOI:
10.46551/ruc.v26n2a4Palavras-chave:
Bees; Flower; Pollination; PollenResumo
Aquí, nós observamos a interação entre Centrosema brasilianum (Fabaceae, Papilionoideae) e seus visitantes florais, quantificando o pólen removido e os atributos dos visitantes. Objetivo: determinar se o comportamento, quantidade e lugar de deposição do pólen no corpo das abelhas visitantes difere de acordo com o tamanho corporal das abelhas. Métodos: os atributos morfológicos e comportamentais tanto florais como das abelhas observadas na interação, foram medidos em 20 indivíduos de C. brasilianum. O lugar de deposição e a quantidade de carga polínica em cada abelha foi identificada. A relação entre os atributos dos interatuantes e o pólen depositado foi determinado utilizando modelos lineares simples. Resultados: O comportamento das abelhas e a deposição de pólen no corpo variaram de acordo com o tamanho corporal das abelhas. Abelhas maiores e com línguas longas levantaram as quilhas florais durante as visitas e a deposição de pólen ocorreu em suas cabeças e superfícies dorsais. Indivíduos menores e com língua curta não levantaram a quilha e o pólen foi depositado na superfície dorsal, mas principalmente nas asas. Além disso, as abelhas maiores tinham o dobro de grãos de pólen depositados na superfície do corpo do que as abelhas menores. Conclusões: Assumimos que abelhas maiores podem fornecer um serviço de polinização mais eficaz do que abelhas menores para C. brasilianum. Implicações: Avaliações futuras devem ser realizadas incluindo mais atributos morfológicos e comportamentais em um número maior de amostras, o que forneceria uma compreensão mais matizada da eficiência da polinização, a relação entre os diferentes comportamentos das abelhas e tamanhos corporais, e as consequências da deposição diferencial de pólen no sucesso reprodutivo de C. brasilianum.
Downloads
Referências
CORLETT, Richard T. Flower visitors and pollination in the Oriental (Indomalayan) Region. Biological Reviews, v. 79, n. 3, p. 497–532. 2004
NE’EMAN, Gigi et al. A framework for comparing pollinator performance: Effectiveness and efficiency. Biological Reviews, v. 85, n. 3, p. 435–451. 2010
KING, Caroline; BALLANTYNE, Gavin; WILLMER, Pat G. Why flower visitation is a poor proxy for pollination: measuring single‐visit pollen deposition, with implications for pollination networks and conservation. Methods in Ecology and Evolution, v. 4, n. 9, p. 811-818, 2013.
WILLMER, Pat; FINLAYSON, Kathryn. Big bees do a better job: intraspecific size variation influences pollination effectiveness. Journal of Pollination Ecology, v. 14, p. 244-254, 2014. DOI:10.26786/1920-7603(2014)22
FÖLDESI Rita et al. Larger pollinators deposit more pollen on stigmas across multiple plant species – A meta-analysis. Journal of Applied Ecology, v. 58 n.4, p. 699–707, 2021.
INOUYE, D. W. The ecology of nectar robbing. The Biology of Nectaries. In The biology of nectaries. Eds B Bentley, T Elias. New York: Columbia University Press, p. 153–173, 1983.
HEDERSTRÖM, Veronica et al. Do plant ploidy and pollinator tongue length interact to cause low seed yield in red clover? Ecosphere, v. 12, n. 3, p. e03416, 2021.
PHILLIPS, Benjamin B. et al. Shared traits make flies and bees effective pollinators of oilseed rape (Brassica napus L.). Basic and Applied Ecology, v. 32, p. 66-76, 2018. https://doi.org/10.1016/j.baae.2018.06.004
STAVERT, Jamie R. et al. Hairiness: the missing link between pollinators and pollination. PeerJ, v. 4, p. e2779, 2016.https://doi.org/10.7717/peerj.2779
CONNER, Jeffrey K.; DAVIS, Rachel; RUSH, Scott. The effect of wild radish floral morphology on pollination efficiency by four taxa of pollinators. Oecologia, v. 104, p. 234-245, 1995.https://doi.org/10.1007/BF00328588
PARK, Mia G. et al. Per-visit pollinator performance and regional importance of wild Bombus and Andrena (Melandrena) compared to the managed honey bee in New York apple orchards. Apidologie, v. 47 n. 2, p. 145–160, 2016. https://doi.org/10.1007/s13592-015-0383-9
THOMSON, James D.; GOODELL, Karen. Pollen removal and deposition by honeybee and bumblebee visitors to apple and almond flowers. Journal of Applied ecology, v. 38 n. 5, p. 1032-1044, 2001.
MORRIS, William F.; VÁZQUEZ, Diego P.; CHACOFF, Natacha P. Benefit and cost curves for typical pollination mutualisms. Ecology, v. 91, n. 5, p. 1276-1285, 2010.
NATTERO, Julieta; COCUCCI, Andrea Aristides; MEDEL, R. Pollinator‐mediated selection in a specialized pollination system: matches and mismatches across populations. Journal of Evolutionary Biology, v. 23, n. 9, p. 1957-1968, 2010.
SOLÍS‐MONTERO, Lislie; VALLEJO‐MARÍN, Mario. 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, v. 7, n. 8, p. 2706-2715, 2017.
OLLERTON, Jeff; WINFREE, Rachael; TARRANT, Sam. How many flowering plants are pollinated by animals?. Oikos, v. 120, n. 3, p. 321-326, 2011.
DAFNI, Amots; KEVAN, Peter G. Flower size and shape: implications in pollination. Israel Journal of Plant Sciences, v. 45, n. 2-3, p. 201-211, 1997.
BRUNET, Johanne et al. The effects of flower, floral display, and reward sizes on bumblebee foraging behavior when pollen is the reward and plants are dichogamous. International Journal of Plant Sciences, v. 176, n. 9, p. 811-819, 2015.
E‐VOJTKÓ, Anna et al. The neglected importance of floral traits in trait‐based plant community assembly. Journal of Vegetation Science, v. 31, n. 4, p. 529-539, 2020.DOI: 10.1111/jvs.12877
STOUT, Jane Catherine. Does size matter? Bumblebee behaviour and the pollination of Cytisus scoparius L.(Fabaceae). Apidologie, v. 31, n. 1, p. 129-139, 2000.
PEAT, James; TUCKER, James; GOULSON, Dave. Does intraspecific size variation in bumblebees allow colonies to efficiently exploit different flowers?. Ecological Entomology, v. 30, n. 2, p. 176-181, 2005.
LÁZARO, Amparo; HEGLAND, Stein Joar; TOTLAND, Ørjan. The relationships between floral traits and specificity of pollination systems in three Scandinavian plant communities. Oecologia, v. 157, p. 249-257, 2008.
ARMBRUSTER, W. Scott; MUCHHALA, Nathan. Associations between floral specialization and species diversity: cause, effect, or correlation?. Evolutionary Ecology, v. 23, p. 159-179, 2009.
ARMBRUSTER, W. Scott; MUCHHALA, Nathan. Associations between floral specialization and species diversity: cause, effect, or correlation?. Evolutionary Ecology, v. 23, p. 159-179, 2009.
ENDRESS, Peter K.; FRIIS, Else M. Early Evolution of Flowers. Vienna: Springer Science & Business Media, 2012.
CARDEL, Yuria J.; KOPTUR, Suzanne. Effects of florivory on the pollination of flowers: an experimental field study with a perennial plant. International Journal of Plant Sciences, v. 171, n. 3, p. 283-292, 2010.
AMARAL-NETO, Laércio P.; WESTERKAMP, Christian; MELO, Gabriel AR. From keel to inverted keel flowers: functional morphology of “upside down” papilionoid flowers and the behavior of their bee visitors. Plant Systematics and Evolution, v. 301, p. 2161-2178, 2015.
MAASS, Brigitte L.; TORRES GONZÁLEZ, Alba Marina. Outcrossing in the tropical forage legume Centrosema brasilianum (L.) Benth. Proc. XIIIth Eucarpia Congress. Angers, France, 1992.
WESTERKAMP, Christian; CLASSEN-BOCKHOFF, Regine. Bilabiate flowers: the ultimate response to bees?. Annals of botany, v. 100, n. 2, p. 361-374, 2007. https://doi.org/10.1093/aob/mcm123.
ETCHEVERRY, Angela Virginia; VOGEL, Stefan. Interactions between the asymmetrical flower of Cochliasanthus caracalla (Fabaceae: Papilionoideae) with its visitors. Flora, v. 239, p. 141-150, 2018.https://doi.org/10.1016/j.flora.2017.10.006
ULUER, Deniz. A review for the pollinators of Papilionaceous flowers. Turkish Journal of Biodiversity, v. 4, n. 1, p. 36-52, 2021.
RAMALHO, Mauro; SILVA, Maise; CARVALHO, Gilson. Pollinator sharing in specialized bee pollination systems: a test with the synchronopatric lip flowers of Centrosema Benth (Fabaceae). Sociobiology, v. 61, n. 2, p. 189-197, 2014.
APONTE, Yannely; JÁUREGUI, Damelis. Morfoanatomía floral y algunos aspectos reproductivos de cinco especies de Centrosema (dc.) benth. (Fabaceae). Ernstia, v. 29 n. 2, p. 1-40, 2019.
FAEGRI, Knut; VAN DER PIJL, Leendert. The principles of pollination ecology. Pergamon Press. 1979.
CÓRDOBA, Silvina A.; COCUCCI, Andrea A. Flower power: its association with bee power and floral functional morphology in papilionate legumes. Annals of Botany, v. 108, n. 5, p. 919–931, 2011.
FRANKIE, G. W. et al. Characterstics and organization of the large bee pollination system in the Costa Rican dry forest. CABI Digital databases, p. 411-447, 1983. 19840215560
DANIELI‐SILVA, Aline et al. Do pollination syndromes cause modularity and predict interactions in a pollination network in tropical high‐altitude grasslands?. Oikos, v. 121, n. 1, p. 35-43, 2012.
FAEGRI, Knut; VAN DER PIJL, Leendert. Principles of pollination ecology. 2013.
FENSTER, Charles B. et al. Pollination syndromes and floral specialization. Annu. Rev. Ecol. Evol. Syst., v. 35, p. 375-403, 2004.
FOX, John; WEISBERG, Sanford. An R Companion to Applied Regression, Third edition. Sage publications, Thousand Oaks CA. 2019 https://socialsciences.mcmaster.ca/jfox/Books/Companion/.
HARTIG, Florian. DHARMa: residual diagnostics for hierarchical (multi-level/mixed) regression models. R Packag version 020, 2018.
TEAM, R. Core. R: A language and environment for statistical computing. R Foundation for Statistical Computing, Vienna, Austria. 2021. URL https://www.R-project.org/.
FRANKIE G. W. et al. Characteristics and organization of the large bee pollination system in the Costa Rican dry forest. In: Handbook of experimental pollination biology. Eds C Jones, R Little. New York: Van Nostrand Reinhold Company, p 411–447.
BORGES, Hélida Bruno Nogueira. Biologia reprodutiva de Centrosema pubescens Benth: (Fabaceae). Boletim do Museu Paraense Emilio Goeldi2, v. 1, n. 1, p. 31–38, 2006.
LEPPIK, Elmar Emil. Floral evolution and pollination in the Leguminosae. In: Annales Botanici Fennici. Societas Zoologica Botanica Fennica Vanamo, v. 3, p. 299–308, 1966.
VALLEJO‐MARÍN, Mario et al. Division of labour within flowers: Heteranthery, a floral strategy to reconcile contrasting pollen fates. Journal of Evolutionary Biology, v. 22, n. 4, p. 828–839, 2009. DOI: 10.1111/j.1420-9101.2009.01693.x
LUNAU, Klaus et al. Just spines—mechanical defense of malvaceous pollen against collection by corbiculate bees. Apidologie, v. 46, p. 144-149, 2015. DOI: 10.1007/s13592-014-0310-5
WESTERKAMP, Christian. Keel blossoms: bee flowers with adaptations against bees. Flora, v. 192, n. 2, p. 125-132, 1997.
PARKER, Ingrid M. et al. Pollination of Cytisus scoparius (Fabaceae) and Genista monspessulana (Fabaceae), two invasive shrubs in California. Madroño, v. 49, p. 25–32. 2002
BUCHMANN, Stephen L. et al. Buzz pollination in angiosperms. In: Handbook of experimental pollination biology. Eds CE Jones, RJ Little. New York; Scientific and Academic Editions, Van Reinhold, p. 73–113, 1983.
KOCH, Laura; LUNAU, Klaus; WESTER, Petra. To be on the safe site – Ungroomed spots on the bee’s body and their importance for pollination (Ed. RM Borges). PLOS ONE, v. 12, n. 9, p. e0182522. 2017.
DAFNI, A.; LEHRER, M.; KEVAN, P. G. Spatial flower parameters and insect spatial vision. Biological Reviews, v. 72, n. 2, p. 239-282, 1997.