Orchid bees enhance seed set production of an understory herb in the Western Brazilian Amazon

Authors

DOI:

https://doi.org/10.26786/1920-7603(2023)757

Keywords:

Calathea, Eulaema, Euglossini, floral ecology, inflorescences

Abstract

Bee pollination is an important ecosystem service related to the maintenance of many flowering plants. We evaluated the relationship between orchid bee foraging time and the density of flowering plants and whether visitation varied according to the sex and size class of bees, using Calathea mansonis as a model species. We monitored 10 plots between December 2009 and November 2010 in a forest fragment in Senador Guiomard, Acre, Brazil. We counted the number of flowering plants and flowers per plant and the behaviour of the observed bees. Additionally, we compared the bagged and exposed inflorescences for self-compatibility analysis. We sampled 173 orchid bees from 13 species, with Eulaema cingulata as the most abundant visitor. Eulaema (large bees) were more effective pollinators than Euglossa (small bees). We also found Eulaema polyzona individuals feeding on a Marantaceae species for the first time. The time spent by the bees visiting flowers did not differ with the density of flowering plants or the number of flowers per plant. However, flowers exposed to visitors produced 35% more seeds and 15% heavier seeds than bagged flowers. Considering plant–bee interactions, orchid bees may increase gene flow and compensate for the clonal reproduction of this herb.

References

Aizen MA, Ashworth L, Galetto L (2002) Reproductive success in fragmented habitats: do compatibility systems and pollination specialization matter? Journal of Vegetation Science 13: 885-892. https://doi.org/10.1111/j.1654-1103.2002.tb02118.x DOI: https://doi.org/10.1111/j.1654-1103.2002.tb02118.x

Alvares CA, Stape JL, Sentelhas PC, Gonçalves JLM, Sparovek G (2014) Köppen’s climate classification map for Brazil. Meteorologische Zeitschrift 22: 711-728. https://doi.org/10.1127/0941-2948/2013/0507 DOI: https://doi.org/10.1127/0941-2948/2013/0507

Barreto AA, Freitas L (2007) Atributos florais em um sistema de polinização especializado: Calathea cylindrica (Roscoe) K. Schum. (Marantaceae) e abelhas Euglossina. Revista Brasileira de Botânica 30: 421-431. https://doi.org/10.1590/S0100-84042007000300008 DOI: https://doi.org/10.1590/S0100-84042007000300008

Brosi BJ (2009) The effects of forest fragmentation on euglossine bee communities (Hymenoptera: Apidae: Euglossini). Biological Conservation 142: 414-423. https://doi.org/10.1016/j.biocon.2008.11.003 DOI: https://doi.org/10.1016/j.biocon.2008.11.003

Bruna EM, Kress WJ (2002) Habitat fragmentation and the demographic structure of an Amazonian understory herb (Heliconia acuminata). Conservation Biology 16: 1256-1266. https://doi.org/10.1046/j.1523-1739.2002.99494.x DOI: https://doi.org/10.1046/j.1523-1739.2002.99494.x

Burckle LA, Marlin JC, Knight TM (2013) Plant-pollinator interactions over 120 years: loss of species, co-occurrence, and function. Science 339: 1611-1615. https://doi.org/10.1126/science.1232728 DOI: https://doi.org/10.1126/science.1232728

De Marco P, Coelho FM (2004) Services performed by the ecosystem: forest remnants influence agricultural cultures’ pollination and production. Biodiversity and Conservation 13: 1245-1255. https://doi.org/10.1023/B:BIOC.0000019402.51193.e8 DOI: https://doi.org/10.1023/B:BIOC.0000019402.51193.e8

Dodson CH (1970) The role of chemical attractants in orchid pollination. In: Chambers KL (Ed). Biochemical Coevolution, Corvallis, Oregon State University Press, pp 83-107.

Dodson CH, Frymire GP (1961) Natural pollination of orchids. Missouri Botanical Garden Bulletin 49: 133-139. DOI: https://doi.org/10.2307/2394740

Dressler RL (1982a) Biology of the orchid bees (Euglossini). Annual Review of Ecology and Systematics 13: 373-394. https://doi.org/10.1146/annurev.es.13.110182.002105 DOI: https://doi.org/10.1146/annurev.es.13.110182.002105

Dressler RL (1982b) New species of Euglossa (Hymenoptera: Apidae). Revista de Biologia Tropical 30: 121-150.

Farias RCAP, Madeira-da-Silva MC, Pereira-Peixoto MH, Martins CF (2007) Horário de atividade de machos de Euglossina (Hymenoptera: Apidae) e preferência por fragrâncias artificiais em mata e dunas na Área de Proteção Ambiental da Barra do Rio Mamanguape, Rio Tinto, PB. Neotropical Entomology 36: 863-867. https://doi.org/10.1590/S1519-566X2007000600006 DOI: https://doi.org/10.1590/S1519-566X2007000600006

Forzza RC (2007) Flora da Reserva Ducke, Amazonas, Brasil: Marantaceae. Rodriguésia 58(3): 533-543. https://doi.org/10.1590/2175-7860200758304 DOI: https://doi.org/10.1590/2175-7860200758304

Garibaldi LA, Steffan-Dewenter I, Winfree R, Aizen MA, Bommarco R, Cunningham SA, Kremen C, Carvalheiro LG, Harder LD, Afik O, et al (2013) Wild pollinators enhance fruit set of crops regardless of honey bee abundance. Science 29 (6127): 1608-1611. https://doi.org/10.1126/science.1230200 DOI: https://doi.org/10.1126/science.1230200

Garófalo CA, Rozen Jr JG (2001). Parasitic behavior of Exaerete smaragdina with descriptions of its mature oocyte and larval instars (Hymenoptera: Apidae: Euglossini). American Museum Novitates 3349: 1-28. https://doi.org/10.1206/0003-0082(2001)349<0001:PBOESW>2.0.CO;2 DOI: https://doi.org/10.1206/0003-0082(2001)349<0001:PBOESW>2.0.CO;2

Goulson D (1999). Foraging strategies of insects for gathering nectar and pollen, and implications for plant ecology and evolution. Perspectives in Plant Ecology, Evolution and Systematics 2(2): 185-209. https://doi.org/10.1078/1433-8319-00070 DOI: https://doi.org/10.1078/1433-8319-00070

Greenleaf SS, Kremen C (2006) Wild bee species increase tomato production and respond differently to surrounding land use in Northern California. Biological Conservation 133: 81-87. https://doi.org/10.1016/j.biocon.2006.05.025 DOI: https://doi.org/10.1016/j.biocon.2006.05.025

Hoffman D (2001) As plantas e a cestaria Baniwa. Instituto Socioambiental e Organização Indígena da Bacia do Içana, São Gabriel da Cachoeira.

Horvitz CC, Schemske DW. 1986. Ant-nest soil and seedling growth in a neotropical ant-dispersed herb. Oecologia 70: 318-320. https://doi.org/10.1007/BF00379258 DOI: https://doi.org/10.1007/BF00379258

Horvitz CC, Ehrlén J, Matlaga D (2010). Context-dependent pollinator limitation in stochastic environments: can increased seed set overpower the cost of reproduction in an understorey herb? Journal of Ecology 98: 268–278. https://doi.org/10.1111/j.1365-2745.2009.01628.x DOI: https://doi.org/10.1111/j.1365-2745.2009.01628.x

Instituto Nacional de Meteorologia – IMET (2013) Estação Automática Rio Branco (AC). www.inmet.gov.br.

Janzen DH (1971) Euglossine bees as long-distance pollinators of tropical plants. Science 171: 203-205. https://doi.org/10.1126/science.171.3967.203 DOI: https://doi.org/10.1126/science.171.3967.203

Kennedy H (1978) Systematics and pollination of the “closed-flowered” species of Calathea (Marantaceae). University of California Publication in Botany 71: 1-90.

Kennedy H (2000) Diversification in pollination mechanisms in the Marantaceae. In: Wilson KL, Morrison DA (Eds). Monocots: Systematics and Evolution. Collingwood, CSIRO Publishing, pp 335-344.

Klein AM, Steffan-Dewenter I, Tscharntke T (2003) Bee pollination and fruit set of Coffea arabica and C. canephora (Rubiaceae). American Journal of Botany 90(1): 153-157. https://doi.org/10.3732/ajb.90.1.153 DOI: https://doi.org/10.3732/ajb.90.1.153

Klinkhamer PGL, Metz JAJ (1994) Why plants can be too attractive - a discussion of measures to estimate male fitness. Journal of Ecology 82: 191-194. https://doi.org/10.2307/2261399 DOI: https://doi.org/10.2307/2261399

Kress WJ, Beach JH (1994) Flowering plant reproductive systems. In: Mcdade LA, Bawa KS, Hartshorn GS, et al., editors. La Selva: Ecology and Natural History of a Lowland Tropical Rainforest. Chicago, University of Chicago Press, pp 161-182.

Kroodsma DE (1975) Flight distances of male euglossine bees in orchid pollination. Biotropica 7(1): 71-72. https://doi.org/10.2307/2989803 DOI: https://doi.org/10.2307/2989803

Leite AV, Machado IC (2007) Fenologia reprodutiva, biologia floral e polinizadores de duas espécies simpátricas de Marantaceae em um fragmento de floresta atlântica, Nordeste do Brasil. Revista Brasileira de Botânica 2: 221-231. https://doi.org/10.1590/S0100-84042007000200007 DOI: https://doi.org/10.1590/S0100-84042007000200007

Milfont MO, Rocha EEM, Lima AON, Freitas BM (2013) Higher soybean production using honeybee and wild pollinators, a sustainable alternative to pesticides and auto pollination. Environmental Chemistry Letters 11: 335-341. https://doi.org/10.1007/s10311-013-0412-8 DOI: https://doi.org/10.1007/s10311-013-0412-8

Moure JS (2003) As espécies do gênero Eulaema Lepeletier, 1841 (Hymenoptera, Apidae, Euglossinae). Acta Biológica Paranaense 29: 1-70. https://doi.org/10.5380/abpr.v29i0.582 DOI: https://doi.org/10.5380/abpr.v29i0.582

Ne’eman G, Jurgens A, Newstrom-Lloyd L, Potts SG, Dafni A (2010) A framework for comparing pollinator performance: effectiveness and efficiency. Biological Reviews 85: 435-451. https://doi.org/10.1111/j.1469-185X.2009.00108.x DOI: https://doi.org/10.1111/j.1469-185X.2009.00108.x

Nemésio A (2009) Orchid bees (Hymenoptera: Apidae) of the Brazilian Atlantic Forest. Zootaxa, 2041: 1-242. http://www.mapress.com/zootaxa/2009/f/z02041p242f.pdf DOI: https://doi.org/10.11646/zootaxa.2041.1.1

Nemésio A (2013) Are orchid bees at risk? First comparative survey suggests declining populations of forest-dependent species. Brazilian Journal of Biology 73: 367-374. https://doi.org/10.1590/S1519-69842013000200017 DOI: https://doi.org/10.1590/S1519-69842013000200017

Ollerton J, Winfree R, Tarrant S (2011) How many flowering plants are pollinated by animals? Oikos 120(3): 321-326. https://doi.org/10.1111/j.1600-0706.2010.18644.x DOI: https://doi.org/10.1111/j.1600-0706.2010.18644.x

Oliveira ML (1999) Sazonalidade e horário de atividade de abelhas Euglossinae (Hymenoptera, Apidae), em florestas de terra firme na Amazônia Central. Revista Brasileira de Zoologia 16(1): 83-90. https://doi.org/10.1590/S0101-81751999000100003 DOI: https://doi.org/10.1590/S0101-81751999000100003

Pischtschan E, Claβen-Bockhoff R (2008) Setting-up tension in the style of Marantaceae. Plant Biology (Stuttg) 10: 441-450. https://doi.org/10.1111/j.1438-8677.2008.00051.x DOI: https://doi.org/10.1111/j.1438-8677.2008.00051.x

R Development Core Team (2017) R: A language and environment for statistical computing. Vienna, Austria: R Foundation for Statistical Computing.

Ramírez S, Dressler RL, Ospina M (2002) Abejas euglosinas (Hymenoptera: Apidae) de la Región Neotropical: Listado de especies con notas sobre su biologia. Biota Colombiana 3: 7-118. http://hdl.handle.net/20.500.11761/32604

Ricketts TH, Daily GC, Ehrlich PR, Michener CD (2004) Economic value of tropical forest to coffee production. Proceedings of the National Academy of Sciences 101(34): 12579–12582. https://doi.org/10.1073/pnas.0405147101 DOI: https://doi.org/10.1073/pnas.0405147101

Roubik DW (2002) Tropical agriculture: The value of bees to the coffee harvest. Nature 417: 708. https://doi.org/10.1038/417708a DOI: https://doi.org/10.1038/417708a

Sahli HF, Connor JK (2007) Visitation, effectiveness, and efficiency of 15 genera of visitors to wild radish Raphanus raphanistrum (Brassicaceae). American Journal of Botany 94(2): 203-209. https://doi.org/10.3732/ajb.94.2.203 DOI: https://doi.org/10.3732/ajb.94.2.203

Schemske DW, Horvitz CC (1988) Plant-animal interactions and fruit production in a neotropical herb: A Path Analysis. Ecology 69(4): 1128-1137. https://doi.org/10.2307/1941267 DOI: https://doi.org/10.2307/1941267

Steffan-Dewenter I, Tscharntke T (1999) Effects of habitat isolation on pollinator communities and seed set. Oecologia 121: 432-440. https://doi.org/10.1007/s004420050949 DOI: https://doi.org/10.1007/s004420050949

Storck-Tonon D, Morato EF, Oliveira ML (2009) Fauna de Euglossina (Hymenoptera: Apidae) da Amazônia Sul Ocidental, Acre, Brasil. Acta Amazonica 39: 693-706. https://doi.org/10.1590/S0044-59672009000300026 DOI: https://doi.org/10.1590/S0044-59672009000300026

Tonhasca Jr A, Blackmer JL, Albuquerque GS (2002) Abundance and diversity of euglossine bees in the fragmented landscape of the Brazilian Atlantic Forest. Biotropica 34: 416-422. https://doi.org/10.1111/j.1744-7429.2002.tb00555.x DOI: https://doi.org/10.1111/j.1744-7429.2002.tb00555.x

Wikelski M, Moxley J, Eaton-Mordas A, López-Uribe MM, Holland R, Moskowitz D, Roubik DW, Kays R (2010) Large-range movements of neotropical orchid bees observed via radio telemetry. PLoS One 5 (5): e10738. https://doi.org/10.1371/journal.pone.0010738 DOI: https://doi.org/10.1371/journal.pone.0010738

Wilcock C, Neiland R (2002) Pollination failure in plants: why it happens and when it matters. Trends in Plant Science 7: 270-277. https://doi.org/10.1016/S1360-1385(02)02258-6 DOI: https://doi.org/10.1016/S1360-1385(02)02258-6

Williams NH, Dodson CH (1972) Selective attraction of male euglossine bees to orchid floral fragrances and its importance in long-distance pollen flow. Evolution 26:84-95. https://doi.org/10.2307/2406985 DOI: https://doi.org/10.1111/j.1558-5646.1972.tb00176.x

Yeo P (1993) Secondary pollen presentation: Form, Function and Evolution. Plant Systematics and Evolution 6: 1-268. https://doi.org/10.1007/978-3-7091-6670-3 DOI: https://doi.org/10.1007/978-3-7091-6670-3_1

Published

2023-12-15

How to Cite

Brito, T., Silva, D. ., Contrera, F., Maués, M., & Morato, E. (2023). Orchid bees enhance seed set production of an understory herb in the Western Brazilian Amazon. Journal of Pollination Ecology, 35, 284–295. https://doi.org/10.26786/1920-7603(2023)757

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