Skip to main content
Log in

Nectar production dynamics and sugar composition in two Mucuna species (Leguminosae, Faboideae) with different specialized pollinators

  • Original Paper
  • Published:
Naturwissenschaften Aims and scope Submit manuscript

Abstract

Nectar is secreted in particular rhythms throughout the lifespan of a flower, which allows determining the nectar production dynamics. This paper compares nectar features in Mucuna japira and Mucuna urens describing: dynamics of nectar production, floral response to nectar removal, resorption, nectar sugar composition, and variation in nectar sugar composition. M. japira inflorescence bears 12–21 yellow flowers, which are in anthesis for 7 days, whereas M. urens inflorescence bears 36–54 greenish flowers, but only 1–3 flowers are in anthesis simultaneously that last one night. Nectar volume and sugar concentration were measured, and the amount of sugar was estimated. Qualitative and quantitative nectar sugar composition was determined. Both species had a constant nectar sugar concentration (ca. 10% for M. japira and ca. 16% for M. urens) and secreted high volumes of nectar (ca. 340 μl per flower for M. japira and 310 μl per flower for M. urens), during 5 days for M. japira and 6 h for M. urens, but after the first removal, i.e., when flower opening mechanism is triggered, nectar production stops immediately. Nectar resorption occurred in both species. Nectar sugar composition showed some similarities between the species. Variation in nectar sugar composition occurred in both species. The Mucuna species are dependent on their pollinators to produce fruits and seeds, and they have different strategies to promote the necessary interaction with birds or bats, especially related to nectar and flower characteristics.

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

Similar content being viewed by others

References

  • Agostini K (2008) Ecologia da reprodução de duas species de Mucuna (Leguminosae, Faboideae, Phaseoleae)—embriologia, citogenética e variabilidade genética—do litoral norte de São Paulo. Thesis. Universidade Estadual de Campinas

  • Agostini K, Sazima M, Sazima I (2006) Bird pollination of explosive flowers while foraging for nectar and caterpillars. Biotropica 38:674–678

    Article  Google Scholar 

  • Agostini K, Sazima M, Tozzi AMGA, Forni-Martins ER (2009) Microsporogenesis and pollen morphology of Mucuna japira Azevedo, Agostini & Sazima and M. urens (L.) Medikus. Phytomorphology 59:61–69

    Google Scholar 

  • Arroyo MTK (1981) Breeding systems and pollination biology in Leguminosae. In: Polhill RM, Raven PH (eds) Advances in legume systematics, part 2. Royal Botanic Garden, Kew, pp 723–769

    Google Scholar 

  • Baker HG (1970) Bat pollination in Central America. Rev Biol Trop 17:187–197

    Google Scholar 

  • Baker HG (1975) Sugar concentration in nectars from hummingbird flowers. Biotropica 7:37–41

    Article  Google Scholar 

  • Baker HG, Baker I (1983) Floral nectar sugar constituents in relation to pollinator type. In: Jones CE, Little RJ (eds) Handbook of experimental pollination biology. Van Nostrand Reinhold Co., New York, pp 117–141

    Google Scholar 

  • Baker HG, Baker I, Hodges SA (1998) Sugar composition of nectars and fruits consumed by birds and bats in the tropics and subtropics. Biotropica 30:559–586

    Article  Google Scholar 

  • Bernardello LM, Galetto L, Jaramillo J, Grijalba E (1994) Floral nectar and chemical composition of some species from Reserva Río Guajalito, Ecuador. Biotropica 26:113–116

    Article  Google Scholar 

  • Biernaskie JM, Cartar RV (2004) Variation in rate of nectar production depends on floral display size: a pollinator manipulation hypothesis. Funct Ecol 18:125–129

    Article  Google Scholar 

  • Bolten AB, Feinsinger P (1978) Why do hummingbird flowers secrete dilute nectar? Biotropica 10:307–309

    Article  Google Scholar 

  • Búrquez A, Corbet SA (1991) Do flowers reabsorb nectar? Funct Ecol 5:369–379

    Article  Google Scholar 

  • Calder WA (1979) On the temperature-dependency of optimal nectar concentrations for birds. J Theor Biol 78:185–196

    Article  PubMed  Google Scholar 

  • Canto A, Pérez R, Medrano M, Castellanos MC, Herrera CM (2007) Intra-plant variation in nectar sugar composition in two Aguilegia species (Ranunculaceae): contrasting patterns under field and glasshouse conditions. Ann Bot 99:653–660

    Article  PubMed  CAS  Google Scholar 

  • Castellanos MC, Wilson P, Thomson JD (2002) Dynamic nectar replenishment in flowers of Penstemon (Scrophulariaceae). Am J Bot 89:111–118

    Article  PubMed  Google Scholar 

  • Cocucci AA, Galetto L, Sérsic A (1992) El síndrome floral de Caesalpinia gilliesii (Fabaceae—Caesalpinioideae). Darwiniana 31:111–135

    Google Scholar 

  • Cruden RW, Hermann SM, Peterson S (1983) Patterns of nectar production and plant–pollinator coevolution. In: Bentley B, Elias TS (eds) The biology of nectaries. Columbia University Press, New York, pp 80–125

    Google Scholar 

  • Digby PGN, Kempton RA (1996) Multivariate analysis of ecological communities. Chapman and Hall, London

    Google Scholar 

  • Endress PK (1994) Diversity and evolutionary biology of tropical flowers. Cambridge University Press, Cambridge

    Google Scholar 

  • Faegri K, van der Pijl L (1980) The principles of pollination ecology. Pergamon Press, New York

    Google Scholar 

  • Freeman CE, Worthington RD, Jackson MS (1991) Floral nectar sugar compositions of some South and Southeast Asian species. Biotropica 23:568–574

    Article  Google Scholar 

  • Galetto L, Bernardello L (1992) Nectar secretion pattern and removal effects in six Argentinean Pitcairnioideae (Bromeliaceae). Bot Acta 105:292–299

    Google Scholar 

  • Galetto L, Bernardello G (1993) Nectar secretion pattern and removal effects in three species of Solanaceae. Can J Bot 71:1394–1398

    Article  Google Scholar 

  • Galetto L, Bernardello G (1995) Characteristics of nectar secretion by Lycium cestroides, L. ciliatum (Solanaceae) and their hybrid. Plant Species Biol 11:157–163

    Article  Google Scholar 

  • Galetto L, Bernardello G (2003) Nectar sugar composition in angiosperms from Chaco and Patagonia (Argentina): an animal visitor's matter? Plant Syst Evol 238:69–86

    CAS  Google Scholar 

  • Galetto L, Bernardello G (2004) Floral nectaries, nectar production dynamics and chemical composition in six Ipomoea species (Convolvulaceae) in relation to pollinators. Ann Bot 94:269–280

    Article  PubMed  CAS  Google Scholar 

  • Galetto L, Bernardello G (2005) Nectar. In: Dafni A, Kevan P, Husband BC (eds) Practical pollination biology. Enviroquest, Ontario, pp 261–313

    Google Scholar 

  • Galetto L, Bernardello G, Rivera G (1997) Nectar, nectaries, flower visitors, and breeding system in some Argentinean Orchidaceae. J Plant Res 110:393–403

    Article  Google Scholar 

  • Galetto L, Bernardello G, Isele IC, Vesprini J, Speroni G, Berdue A (2000) Reproductive biology of Erythrina crista-galli (Fabaceae). Ann Mo Bot Gard 87:127–145

    Article  Google Scholar 

  • Herrera CM, Pérez R, Alonso C (2006) Extreme intra-plant variation in nectar sugar composition in an insect-pollinated perennial herb. Am J Bot 93:575–581

    Article  PubMed  Google Scholar 

  • Johnson SD, Nicolson SW (2008) Evolutionary associations between nectar properties and specificity in bird pollination systems. Biol Lett 4:49–52

    Article  PubMed  Google Scholar 

  • Koehler A, Verburgt L, McWhorter TJ, Nicolson SW (2010) Energy management on a nectar diet: can sunbirds meet the challenges of low temperature and dilute food? Funct Ecol. doi:10.1111/j.1365-2435.2010.01728.x

  • Ladley JJ, Kelly D, Robertson AW (1997) Explosive flowering, nectar production, breeding systems, and pollinators of New Zealand mistletoes (Loranthaceae). New Zeal J Bot 35:345–360

    Google Scholar 

  • Lotz CN, Schondube JE (2006) Sugar preferences in nectar- and fruit-eating birds: behavioral patterns and physiological causes. Biotropica 38:3–15

    Google Scholar 

  • Luyt R, Johnson SD (2002) Postpollination nectar reabsorption and its implications for fruit quality in an epiphytic orchid. Biotropica 34:442–446

    Google Scholar 

  • Martínez del Rio C, Baker HG, Baker I (1992) Ecological and evolutionary implications of digestive processes: bird preferences and the sugar constituents of floral nectar and fruit pulp. Experientia 48:544–551

    Article  Google Scholar 

  • Martínez del Rio C, Schondube JE, McWhorter TJ, Herrera LG (2001) Intake responses in nectar feeding birds: digestive and metabolic causes, osmoregulatory consequences, and coevolutionary effects. Am Zool 41:902–915

    Article  Google Scholar 

  • Morgensen HL (1975) Ovule abortion in Quercus (Fagaceae). Am J Bot 62:160–165

    Article  Google Scholar 

  • Musicante ML, Galetto L (2008) Características del néctar de Cologania broussonetti (Balb.) DC. (Fabaceae) y su relación con los visitantes florales. Ecol Austral 18:195–204

    Google Scholar 

  • Nepi M, Stpiczyńska M (2007) Nectar resorption and translocation in Cucurbita pepo L. and Platanthera chlorantha Custer (Rchb.). Plant Biology 9:93–100

    Article  PubMed  CAS  Google Scholar 

  • Nepi M, Stpiczyńska M (2008) The complexity of nectar: secretion and resorption dynamically regulate features. Naturwissenschaften 95:177–184

    Article  PubMed  CAS  Google Scholar 

  • Nicolson SW (2007) Nectar consumers. In: Nicolson SW, Pacini E, Nepi M (eds) Nectaries and nectar. Springer, The Netherlands, pp 289–342

    Chapter  Google Scholar 

  • Ordano M, Ornelas JF (2004) Generous-like flowers: nectar production in two epiphytic bromeliads and a meta-analysis of removal effects. Oecologia 140:495–505

    Article  PubMed  Google Scholar 

  • Petanidou T, van Laere AJ, Smets E (1996) Change in floral nectar components from fresh to senescent flowers of Capparis spinosa (Capparidaceae), a nocturnally flowering Mediterranean shrub. Pl Syst Evol 199:79–92

    Article  Google Scholar 

  • Pizo MA (1996) Feeding ecology of two Cacicus species (Emberizidae, Icterinae). Ararajuba 4:87–92

    Google Scholar 

  • Pyke GH (1991) What does it cost a plant to produce floral nectar? Nature 350:58–59

    Article  Google Scholar 

  • Ragusa-Netto J (2002) Exploitation of Erythrina dominguezii Hassl. (Fabaceae) nectar by perching birds in a dry forest in western Brazil. Braz J Biol 62:877–883

    Article  PubMed  CAS  Google Scholar 

  • Rivera GL, Galetto L, Bernardello G (1996) Nectar secretion pattern, removal effects, and breeding system of Ligaria cuneifolia (Loranthaceae). Can J Bot 74:1996–2001

    Article  Google Scholar 

  • Sazima I, Sazima M (1978) Polinização por morcegos em Mucuna urens (Leguminosae). In: Resumos da XXX Reunião da Sociedade Brasileira para o Progresso da Ciência: p. 419

  • Sazima M, Buzato S, Sazima I (2003) Dyssochroma viridiflorum (Solanaceae): a reproductively bat-dependent epiphyte from the Atlantic rainforest in Brazil. Ann Bot 92:725–730

    Article  PubMed  Google Scholar 

  • Sazima I, Sazima C, Sazima M (2009) A catch-all leguminous tree: Erythrina velutina visited and pollinated by vertebrates at an oceanic island. Aust J Bot 57:26–30

    Article  Google Scholar 

  • Sick H (1985) Ornitologia brasileira, uma introdução. Editora da Universidade de Brasília, Brasília

    Google Scholar 

  • Stiles FG (1978) Ecological and evolutionary implications of bird pollination. Am Zool 18:715–727

    Google Scholar 

  • Stiles FG, Freeman CE (1993) Patterns in floral nectar characteristics in some bird–plant species form Costa Rica. Biotropica 25:191–205

    Article  Google Scholar 

  • Stpiczyńska M (2003a) Nectar resorption in the spur of Platanthera chlorantha Custer (Rchb.) Orchidaceae—structural and microautoradiographic study. Plant Syst Evol 238:119–126

    Google Scholar 

  • Stpiczyńska M (2003b) Incorporation of [3H] sucrose after the resorption of nectar from the spur of Platanthera chlorantha (Custer) Rchb. Can J Bot 81:927–932

    Article  Google Scholar 

  • Sweeley EC, Bentley R, Makita M, Wells WW (1963) Gas liquid chromatography of trimethylsilyl derivatives of sugars and related substances. J Am Chem Soc 85:2497–2507

    Article  CAS  Google Scholar 

  • Torres C, Galetto L (1998) Patterns and implications of floral nectar secretion, chemical composition, removal effects and standing crop in Mandevilla pentlandiana (Apocynaceae). Bot J Linn Soc 127:207–223

    Google Scholar 

  • Tozzi AMGA, Agostini K, Sazima M (2005) A new species of Mucuna Adans. (Leguminosae, Papilionoideae, Phaseoleae) from southeastern Brazil, with a key to Brazilian species. Taxon 54:451–455

    Article  Google Scholar 

  • Van Wyk BE (1993) Nectar sugar composition in southern African Papilionoideae (Fabaceae). Biochem Syst Ecol 21:271–277

    Article  Google Scholar 

  • Voigt CC, Speakman JR (2007) Nectar-feeding bats fuel their high metabolism directly with exogenous carbohydrates. Funct Ecol 21:913–921

    Article  Google Scholar 

  • Von Helversen O (1993) Adaptations of flowers to the pollination by Glossophagine bats. In: Barthlott W (ed) Plant–animal interactions in tropical environments. Museum Alexander Koenig, Bonn, pp 41–59

    Google Scholar 

  • Von Helversen D, von Helversen O (2003) Object recognition by echolocation: a nectar-feeding bat exploiting the flowers of a rain forest vine. J Com Phys A 189:327–336

    Google Scholar 

  • Willson MF (1983) Plant reproductive ecology. John Wiley and Sons, New York

    Google Scholar 

  • Winter Y, von Helversen O (2001) Bats as pollinators: foraging energetics and floral adaptations. In: Chittka L, Thomson JD (eds) Cognitive ecology of pollination. Cambridge University Press, Cambridge, pp 148–170

    Chapter  Google Scholar 

Download references

Acknowledgements

We thank four anonymous reviewers for their constructive criticisms that improved a previous version of this paper, the Instituto Florestal (Parque Estadual da Serra do Mar, Núcleo Picinguaba) for the permit to study pollination biology in protected public lands, Iara Bressan for technical help in the laboratory and Dewey Litwiller for English review. KA had a grant of FAPESP, MS has research grants from CNPq, and LG is a researcher from CONICET. This research was mainly supported by the State of São Paulo Research Foundation (FAPESP) as part of the Thematic Project Functional Gradient (Process Number 03/12595-7), within the BIOTA/FAPESP Program—The Biodiversity Virtual Institute (www.biota.org.br). COTEC/IF 41.065/2005 and IBAMA/CGEN 093/2005 permits. CONICET, SECyT (UNC), FONCYT, CAPES-SPU for additional financial support.

Author information

Authors and Affiliations

Authors

Corresponding author

Correspondence to Kayna Agostini.

Additional information

Communicated by: Sven Thatje

Rights and permissions

Reprints and permissions

About this article

Cite this article

Agostini, K., Sazima, M. & Galetto, L. Nectar production dynamics and sugar composition in two Mucuna species (Leguminosae, Faboideae) with different specialized pollinators. Naturwissenschaften 98, 933 (2011). https://doi.org/10.1007/s00114-011-0844-6

Download citation

  • Received:

  • Revised:

  • Accepted:

  • Published:

  • DOI: https://doi.org/10.1007/s00114-011-0844-6

Keywords

Navigation