Comparative effects of two species of floricolous Metschnikowia yeasts on nectar

Authors

  • Azucena Canto Centro de Investigación Científica de Yucatán
  • Carlos M. Herrera Estación Biológica de Doñana, Consejo Superior de Investigaciones Científicas
  • Isabel M. García Estación Biológica de Doñana, Consejo Superior de Investigaciones Científicas
  • Marina García Estación Biológica de Doñana, Consejo Superior de Investigaciones Científicas
  • Pilar Bazaga Estación Biológica de Doñana, Consejo Superior de Investigaciones Científicas

DOI:

https://doi.org/10.3989/ajbm.2396

Keywords:

Bombus terrestris, fructose, Helleborus foetidus, nectar-living yeasts, Rosmarinus officinalis, sucrose

Abstract


Nectar yeast communities in southern Spain are dominated by two closely-related species, Metschnikowia reukaufii Pitt & M.W. Mill. and M. gruessii Gim.-Jurado (Ascomycota, Saccharomycetales), although they tend to be distributed differentially across different host plants. We explore here the possibility that the two yeasts play different functional roles in floral nectar by differing in their impact on sugar concentration and composition of nectar. Experiments were undertaken under controlled conditions using bumblebees caught foraging on the flowers of two different host plants each of which is known to harbor predominantly one of the two yeasts. Bumblebees were used as sources of inocula to obtain two groups of samples from the nectar of Helleborus foetidus L. (Ranunculaceae): nectar samples inoculated with M. gruessii and samples inoculated with M. reukaufii. Metschnikowia gruessii was poorly represented in nectar samples, while M. reukaufii was by far the most common and had the highest cell density. Although the two yeasts caused relatively similar changes in nectar sugar composition, which involved increasing fructose and decreasing sucrose proportions, they marginally differed in their quantitative impact on total nectar sugar concentration. Results suggest that differential yeast occurrence across host plants may lead to yeast specialization and modify the outcomes of the plant-pollinator interface.

Downloads

Download data is not yet available.

References

Álvarez-Pérez, S. & Herrera, C.M. 2013. Composition, richness and nonrandom assembly of culturable bacterial–microfungal communities in floral nectar of Mediterranean plants. FEMS Microbiology Ecology 83: 685-699. http://dx.doi.org/10.1111/1574-6941.12027 PMid:23057414

Barnett, J.A., Payne, R.W. & Yarrow, D. 2000. Yeasts: Characteristics and identification, third Ed. Cambridge University Press, Cambridge.

Brysch-Herzberg, M. 2004. Ecology of yeasts in plant–bumblebee mutualism in Central Europe. FEMS Microbiology Ecology 50: 87-100. http://dx.doi.org/10.1016/j.femsec.2004.06.003 PMid:19712367 Canto, A., Herrera, C.M., García, I.M., Pérez, R. & Vaz, M. 2011. Intraplant variation in nectar traits in Helleborus foetidus (Ranunculaceae) as related to floral phase, environmental conditions and pollinator exposure. Flora 206: 668-675. http://dx.doi.org/10.1016/j.flora.2011.02.003

Canto, A., Herrera, C.M., Medrano, M., Pérez, R. & García, I.M. 2008. Pollinator foraging modifies nectar sugar composition in Helleborus foetidus (Ranunculaceae): An experimental test. American Journal of Botany 95: 315-320. http://dx.doi.org/10.3732/ajb.95.3.315 PMid:21632356

Escalante-Pérez, M. & Heil, M. 2013. The production and protection of nectars. In: U. Lu.ttge & al. (eds.), Progress in Botany 74: 239-261. Springer-Verlag, Berlin Heidelberg. http://dx.doi.org/10.1007/978-3-642-30967-0_9

Giménez-Jurado, G. 1992. Metschnikowia gruessii sp. nov., the teleomorph of Nectaromyces reukaufii but not of Candida reukaufii. Systematic and Applied Microbiology 15: 432-438. http://dx.doi.org/10.1016/S0723-2020(11)80218-3

Herrera, C.M., Canto, A., Pozo, M.I. & Bazaga, P. 2010. Inhospitable sweetness: nectar •ltering of pollinator-borne inocula leads to impoverished, phylogenetically clustered yeast communities. Proceedings of the Royal Society B: Biological Sciences 277: 747-754. http://dx.doi.org/10.1098/rspb.2009.1485 PMid:19889702 PMCid:PMC2842741

Herrera, C.M., de Vega, C., Canto, A. & Pozo, M.I. 2009. Yeasts in floral nectar: a quantitative survey. Annals of Botany 103: 1415-1423. http://dx.doi.org/10.1093/aob/mcp026 PMid:19208669 PMCid:PMC2701759

Herrera, C.M., García, I.M. & Pérez, R. 2008. Invisible floral larcenies: microbial communities degrade floral nectar of bumble bee-pollinated plants. Ecology 89: 2369-2376. http://dx.doi.org/10.1890/08-0241.1 PMid:18831156

Herrera, C.M., Pérez, R. & Alonso, C. 2006. Extreme intraplant variation in nectar sugar composition in an insect-pollinated perennial herb. American Journal of Botany 93: 575-581. http://dx.doi.org/10.3732/ajb.93.4.575 PMid:21646218

Herrera, C.M., Pozo, M.I. & Bazaga, P. 2011. Clonality, genetic diversity and support for the diversifying selection hypothesis in natural populations of a flower-living yeast. Molecular Ecology 20: 4395-4407. http://dx.doi.org/10.1111/j.1365-294X.2011.05217.x PMid:21851437

Herrera, C.M., Pozo, M.I. & Bazaga, P. 2012. Jack of all nectars, master of most: DNA methylation and the epigenetic basis of niche width in a flower-living yeast. Molecular Ecology 21: 2602-2616. http://dx.doi.org/10.1111/j.1365-294X.2011.05402.x PMid:22171717

Herrera, C.M., Pozo, M.I. & Medrano, M. 2013. Yeasts in nectar of an early-blooming herb: sought by bumble bees, detrimental to plant fecundity. Ecology 94: 273-279. http://dx.doi.org/10.1890/12-0595.1 PMid:23691645

Herrera, C.M., Sánchez-Lafuente, A.M., Medrano, M., Guitián, J., Cerdá, X. & Rey, P. 2001. Geographical variation in autonomous self-pollination levels unrelated to pollinator service in Helleborus foetidus (Ranunculaceae). American Journal of Botany 88: 1025-1032. http://dx.doi.org/10.2307/2657084 PMid:11410466

Lachance, M.A. 2011. Metschnikowia Kamienski (1899). In: Kurtzman, C.P. & al. (eds.), The yeast, a taxonomic study 1: 575-620. Elsevier, London.

Pozo, M.I., Herrera, C.M. & Bazaga, P. 2011. Species richness of yeast communities in floral nectar of southern Spanish plants. Microbial Ecology 61: 82-91. http://dx.doi.org/10.1007/s00248-010-9682-x PMid:20449581

Pozo, M.I., Lachance, M.A. & Herrera, C.M. 2012. Nectar yeasts of two southern Spanish plants: the roles of immigration and physiological traits in community assembly. FEMS Microbiology Ecology 80: 281-293. http://dx.doi.org/10.1111/j.1574-6941.2011.01286.x PMid:22224447

Simpson, B.B. & Neff, J.L. 1983. Evolution and diversity of floral rewards. In: Jones, C.E. & Little, R.J. (eds.), Handbook of experimental pollination biology 142–159. Van Nostrand Reinhold, New York.

Weber, K. & Ebel, F. 1994. Zur lebensgeschichte der gattung Helleborus L (Ranunculaceae). Flora 189: 97-130.

Downloads

Published

2015-06-30

How to Cite

Canto, A., Herrera, C. M., García, I. M., García, M., & Bazaga, P. (2015). Comparative effects of two species of floricolous Metschnikowia yeasts on nectar. Anales Del Jardín Botánico De Madrid, 72(1), e019. https://doi.org/10.3989/ajbm.2396

Issue

Section

Articles