Skip to main content

Advertisement

Log in

Changes in floristic composition and pollination systems in a “Cerrado” community after 20 years of fire suppression

  • Original Article
  • Published:
Brazilian Journal of Botany Aims and scope Submit manuscript

Abstract

Fire is considered a major factor in the succession process in “Cerrado”, determining the dynamics and composition of these Neotropical savanna plant formations. However, when savannas are protected from fire, both fire-tolerant and fire-sensitive plant species increase in density and size, especially species of trees. Nevertheless, how this change in the vegetation structure relates to changes in the ecosystem function has been seldom evaluated. Pollination is a major ecosystem service, and here we aimed to determine possible changes in floristic composition, floral biology, and pollination systems in an area of open savanna protected against fire over a period of 20 years in Minas Gerais state, Central Brazil. The comparison over the two decades showed that ecological succession, in the absence of fire, increased the diversity and decreased the dominance of plant species. There was an increase in specie richness from 156 spp. in 1992 to 206 spp. in 2012, with appearance of trees and species with specialized pollination systems. Plants were predominantly pollinated by bees in both periods, but floral diversity and specialization seem to have increased after fire suppression, for instance, with the emergence of more species pollinated by moths. Not only generalist light-colored actinomorphic flowers, but also tubular or cup-like nectar flowers commonly associated with more specialized pollinators predominated in both periods. The dominance of these contrasting features actually increased after two decades, especially when we compare the number of individuals in each group. However, it seems that the increase in plant diversity and density of woody species did not lead to marked specialization of floral features and pollination system along the studied period.

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
Fig. 3
Fig. 4

Similar content being viewed by others

References

  • Albrecht M, Riesen M, Schmid B (2010) Plant–pollinator network assembly along the chronosequence of a glacier foreland. Oikos 119:1610–1624

    Article  Google Scholar 

  • Amorim FW, Wyatt GE, Sazima M (2014) Low abundance of long-tongued pollinators leads to pollen limitation in four specialized hawkmoth-pollinated plants in the Atlantic Rain forest, Brazil. Naturwissenschaften 101:893–905

    Article  CAS  PubMed  Google Scholar 

  • Arantes CS, Vale VS, Oliveira AP, Junior JAP, Lopes SF, Schiavini I (2014) Forest species colonizing cerrado open areas: distance and area effects on the nucleation process. Braz J Bot 37:143–150

    Google Scholar 

  • Backéus I (1992) Distribution and vegetation dynamics of humid savannas in Africa and Asia. J Veg Sci 3:45–356

    Article  Google Scholar 

  • Barbosa AAA (1996) Biologia reprodutiva de uma comunidade de campo sujo de cerrado, Uberlândia/MG. Doctoral Thesis, Universidade Estadual de Campinas, Campinas

  • Barbosa AAA, Sazima M (2008) Biologia reprodutiva de plantas herbáceo-arbustivas de uma área de campo sujo de cerrado. In: Sano SM, Almeida SP, Ribeiro JF (eds) Cerrado: ecologia e flora. Embrapa Cerrados, Planaltina, pp 293–318

    Google Scholar 

  • Bawa KS (1990) Plant-pollinator interactions in a tropical rain forest. Ann Rev Ecol Syst 21:399–422

    Article  Google Scholar 

  • Bawa KS, Perry DR, Beach JH (1985) Reproductive biology of tropical lowland rain forest trees. I. Sexual systems and incompatibility mechanisms. Am J Bot 72:331–345

    Article  Google Scholar 

  • Begon M, Harper JL, Towsend CR (2009) Ecologia: de indivíduos a ecossistemas. Artmed, Porto Alegre

    Google Scholar 

  • Blüthgen N, Menzel F, Hovestadt T, Fiala B, Blüthgen N (2007) Specialization, constraints, and conflicting interests in mutualistic networks. Curr Biol 17:41–346

    Article  Google Scholar 

  • Borges HBN (2000) Biologia reprodutiva e conservação do estrato lenhoso numa comunidade do Cerrado. Doctoral thesis, Universidade Estadual de Campinas, Campinas

  • Bremer B, Bremer K, Chase M, Fay M, Reveal J, Soltis D, Soltis P, Stevens P (2009) An update of the Angiosperm Phylogeny Group classification for the orders and families of flowering plants: APG III. Bot J Linn Soc 161:105–121

    Article  Google Scholar 

  • Brower JE, Zar JH, von Ende CN (1998) Field and laboratory methods for general ecology. WCB/McGraw-Hill, New York

    Google Scholar 

  • Brown J, York A, Christie F, McCarthy M (2016) Effects of fire on pollinators and pollination. J Appl Ecol. doi:10.1111/1365-2664.12670

    Google Scholar 

  • Cardoso E, Moreno MIC, Bruna EM, Vasconcelos HL (2009) Mudanças fitofisionômicas no Cerrado: 18 anos de sucessão ecológica na Estação Ecológica do Panga, Uberlândia-MG. Caminhos de Geografia (Uberlandia) 32:254–268

    Google Scholar 

  • Coutinho LM (1977) Aspectos ecológicos do fogo no cerrado. II—as queimadas e a dispersão de sementes em algumas espécies anemocóricas do estrato herbáceo subarbustivo. Bol Bot USP 5:57–64

    Article  Google Scholar 

  • Coutinho LM (1990) Fire in the ecology of the Brazilian Cerrado. In: Goldhammer JG (ed) Fire in the tropical biota. Springer, Berlin, pp 82–105

    Chapter  Google Scholar 

  • Coutinho LM (2002) O bioma do cerrado. In: Klein AL (ed) Eugene warming e o cerrado brasileiro: um século depois. Editora da Unesp, São Paulo, pp 77–91

    Google Scholar 

  • Deus FF, Vale VS, Schiavini I, Oliveira PE (2014) Diversity of reproductive ecological groups in semideciduous seasonal forests. Biosci J 30:1885–1902

    Google Scholar 

  • Durigan G, Ratter JA (2006) Successional changes in cerradão and cerrado/forest ecotonal vegetation in western São Paulo State, Brazil, 1962–2000. Edinb J Bot 63:119–130

    Article  Google Scholar 

  • Durigan G, Siqueira MF, Franco GADC, Bridgewater S, Ratter JA (2003) The vegetation of priority areas for cerrado conservation in São Paulo State, Brazil. Edinb J Bot 60:217–241

    Article  Google Scholar 

  • Ebeling A, Klein AM, Schumacher J, Weisser WW, Tscharntke T (2008) How does plant richness affect pollinator richness and temporal stability of flower visits? Oikos 117:1808–1815

    Article  Google Scholar 

  • Felfili JM, Rezende AV, Silva Júnior MC, Silva MA (2000) Changes in floristic composition of cerrado sensu stricto in Brazil over a 9-year period. J Trop Ecol 16:576–590

    Article  Google Scholar 

  • Felfili JM, Silva Júnior MC, Sevilha AC, Fagg CW, Walter BMT, Nogueira PE, Rezende AV (2004) Diversity, floristic and structural patterns of cerrado vegetation in Central Brazil. Plant Ecol 175:37–46

    Article  Google Scholar 

  • Fensham RJ, Butler DW (2003) Spatial pattern of dry rainforest colonizing unburnt Eucalyptus savanna. Aust Ecol 28:121–128

    Google Scholar 

  • Fensham RJ, Fairfax RJ, Butler DW, Bowman DMJS (2003) Effects of fire and drought in a tropical eucalypt savanna colonized by rain forest. J Biogeogr 30:1405–1414

    Article  Google Scholar 

  • Ferreira C, Maruyama PK, Oliveira PE (2016) Convergence beyond flower morphology? Reproductive biology of hummingbird-pollinated plants in the Brazilian Cerrado. Plant Biol 18:316–324

    Article  CAS  PubMed  Google Scholar 

  • Fontaine C, Dajoz I, Meriguet J, Loreau M (2005) Functional diversity of plant-pollinator interaction webs enhances the persistence of plant communities. PLoS Biol 4:129–135

    Article  Google Scholar 

  • Franco A (2005) Biodiversidade de forma e função: implicações ecofisiológicas das estratégias de utilização de água e luz em plantas lenhosas do Cerrado. In: Scariot A, Souza Silva JC, Felfili JM (eds) Cerrado: ecologia, biodiversidade e conservação. Ministério do Meio Ambiente, Brasília, pp 179–196

    Google Scholar 

  • Gathmann A, Greiler HJ, Tscharntke T (1994) Trap-nesting bees and wasps colonizing set-aside fields: sucession and body size, management by cutting and sowing. Oecologia 98:8–14

    Article  Google Scholar 

  • Geiger EL, Gotsch SG, Damasco G, Haridasan M, Franco AC, Hoffmann WA (2011) Distinct roles of savanna and forest tree species in regeneration under fire suppression in a Brazilian savanna. J Veg Sci 22:312–321

    Article  Google Scholar 

  • Ghazoul J (2006) Floral diversity and the facilitation of pollination. J Ecol 94:295–304

    Article  Google Scholar 

  • Gignoux J, Lahoreau G, Julliard R, Barot S (2009) Establishment and early persistence of tree seedlings in an annually burned savanna. J Ecol 97:484–495

    Article  Google Scholar 

  • Gouveia GP, Felfili JM (1998) Fenologia de comunidades de cerrado e de mata de galeria no Brasil Central. Rev Arvore 22:443–450

    Google Scholar 

  • Grundel R, Jean RP, Frohnapple KJ, Glowacki GA, Scott PE, Pavlovic NB (2010) Floral and nesting resources, habitat structure, and fire influence bee distribution across an open-forest gradient. Ecol Appl 20:1678–1692

    Article  PubMed  Google Scholar 

  • Hegland SJ, Totland O (2005) Relationships between species’ floral traits and pollinator visitation in a temperate grassland. Oecologia 145:586–594

    Article  PubMed  Google Scholar 

  • Henriques RPB (2005) Influência da história, solo e fogo na distribuição e dinâmica das fitofisionomias no bioma do Cerrado. In: Scariot A, Sousa Silva JC, Felfili JM (eds) Cerrado: ecologia, biodiversidade e conservação. Ministério do Meio Ambiente, Brasília pp, pp 75–92

    Google Scholar 

  • Henriques RPB, Hay JD (2002) Patterns and dynamics of plant populations. In: Oliveira PS, Marquis RJ (eds) The Cerrados of Brazil: ecology and natural history of a Neotropical savanna. Columbia University Press, New York, pp 140–158

    Google Scholar 

  • Hoffmann WA, Adasme R, Haridasan M, Carvalho M, Geiger EL, Pereira MAB, Gotsch SG, Franco AC (2009) Tree topkill, not mortality, governs the dynamics of alternate stable states at savanna—forest boundaries under frequent fire in central Brazil. Ecology 90:1326–1337

    Article  PubMed  Google Scholar 

  • Holzschuh A, Steffan-Dewenter IS, Kleijn D, Tscharntke T (2007) Diversity of flower-visiting bees in cereal fields: effects of farming system, landscape composition and regional context. J Appl Ecol 44:41–49

    Article  Google Scholar 

  • Johnson SD, Steiner KE (2000) Generalization versus specialization in plant pollination systems. TREE 15:140–143

    PubMed  Google Scholar 

  • Kevan PG (1983) Floral colors through the insects eye: what they are and what they mean. In: Jones CE, Little RJ (eds) Handbook of experimental pollination biology. Van Nostrand Reinhold, New York, pp 3–49

    Google Scholar 

  • Kwaiser KS, Hendrix SD (2008) Diversity and abundance of bees (Hymenoptera: Apiformes) in native and ruderal grasslands of agriculturally dominated landscapes. Agr Ecosyst Environ 124:200–204

    Article  Google Scholar 

  • Larsson M, Franzen M (2007) Critical resource levels of pollen for the declining bee Andrena hattorfiana (Hymenoptera: Andrenidae). Biol Conserv 134:405–414

    Article  Google Scholar 

  • Lázaro A, Totland O (2014) The influence of floral symmetry, dependence on pollinators and pollination generalization on flower size variation. Ann Bot 114:157–165

    Article  PubMed  PubMed Central  Google Scholar 

  • Libano AM, Felfili JM (2006) Mudanças temporais na composicão florıstica e na diversidade de um cerrado sensu stricto do Brasil Central em um período de 18 anos (1985–2003). Acta Bot Bras 20:927–936

    Article  Google Scholar 

  • Machado IC, Lopes AV (2004) Floral traits and pollination systems in the Caatinga, a Brazilian tropical dry forest. Ann Bot 94:365–376

    Article  PubMed  PubMed Central  Google Scholar 

  • McCann KS (2000) The diversity-stability debate. Nature 405:228–233

    Article  CAS  PubMed  Google Scholar 

  • Meirelles ML, Klink CA, Silva JCS (1997) Um modelo de estado y transiciones para el cerrado brasileño. Ecotropicos 10:45–50

    Google Scholar 

  • Mendonça RC, Felfili JM, Walter BMT, Silva-Jr MC, Rezende AV, Filgueiras TS, Nogueira PE, Fagg CW (2008) Flora Vascular do bioma Cerrado: checklist com 12.356 espécies. In: Sano SM, Almeida SP, Ribeiro JF (eds) Cerrado: ecologia e flora. Planaltina, Embrapa Cerrados, pp 421–1279

    Google Scholar 

  • Miranda HS, Sato MN, Nascimento-Neto R, Aires FS (2009) Fires in the cerrado, the Brazilian savanna. In: Cochrane MA (ed) Tropical fire ecology: climate change, land use, and ecosystem dynamics. Springer, Chichester, pp 427–450

    Chapter  Google Scholar 

  • Moreira AG (2000) Effects of fire protection on savanna structure in Central Brazil. J Biogeogr 27:1021–1029

    Article  Google Scholar 

  • Munhoz CBR, Felfili JM (2007) Reproductive phenology of an herbaceous subshrub layer of a Savannah (Campo Sujo) in the Cerrado Biosphere Reserve I, Brazil. Braz J Biol 67:299–307

    Article  CAS  PubMed  Google Scholar 

  • Oliveira PE, Gibbs PE (2000) Reproductive biology of woody plants in a cerrado community of Central Brazil. Flora 195:311–329

    Google Scholar 

  • Oliveira PE, Moreira AG (1992) Anemocoria em espécies de cerrado e mata de galeria de Brasília-DF. Rev Bras Bot 15:163–174

    Google Scholar 

  • Oliveira PE, Paula FR (2001) Fenologia e biologia reprodutiva de plantas de Matas de Galeria. In: Ribeiro JF, Fonseca CE, Silva JC (eds) Cerrado: caracterização e recuperação de matas de galeria. Planaltina, Brasília, pp 303–332

    Google Scholar 

  • Oliveira PE, Gibbs PE, Barbosa AA (2004) Moth pollination of woody species in the Cerrados of Central Brazil: a case of so much owed to so few? Plant Syst Evol 245:41–54

    Article  Google Scholar 

  • Oliveira Filho AT, Ratter JA (2002) Vegetation physiognomies and woody flora o the cerrado biome. In: Oliveira PS, Marquis RJ (eds) The Cerrados of Brazil: ecology and natural history of a Neotropical savanna. Columbia University Press, New York, pp 91–120

    Chapter  Google Scholar 

  • Parrish JAD, Bazzaz FA (1979) Difference in pollination niche relationships in early and late successional plant communities. Ecology 60:597–610

    Article  Google Scholar 

  • Pinheiro F, Durigan G (2009) Dinâmica espaço-temporal (1962-2006) das fitofisionomias em unidade de conservação do Cerrado no sudeste do Brasil. Braz J Bot 32:441–454

    Article  Google Scholar 

  • Pinheiro F, Ribeiro JF (2001) Síndromes de dispersão de sementes em Matas de Galeria do Distrito Federal. In: Ribeiro JF, Fonseca CE, Silva JC (eds) Cerrado: caracterização e recuperação de matas de galeria. Planaltina, Brasília, pp 335–375

    Google Scholar 

  • Pivello VR, Coutinho LM (1996) A quantitative successional model to assist in the management of Brazilian Cerrados. For Ecol Manag 87:127–138

    Article  Google Scholar 

  • Potts SG, Vulliamy B, Dafni A, Ne’eman G, Willmer P (2003a) Linking bees and flowers: how do floral communities structure pollinator communities? Ecology 84:2628–2642

    Article  Google Scholar 

  • Potts SG, Vulliamy B, Dafni A, Ne’eman G, O’Toole C, Roberts S, Willmer P (2003b) Response of plant–pollinator communities to fire: changes in diversity, abundance and floral reward structure. Oikos 101:103–112

    Article  Google Scholar 

  • Potts SG, Vulliamy B, Roberts S, O’Toole C, Dafni A, Ne’eman G, Willmer P (2004) Nectar resource diversity organises flower-visitor community structure. Entomol Exp Appl 113:103–107

    Article  Google Scholar 

  • Potts SG, Petanidou T, Roberts S, O’Toole C, Hulbert A, Willmer P (2006) Plant-pollinator biodiversity and pollination services in a complex Mediterranean landscape. Biol Conserv 129:519–529

    Article  Google Scholar 

  • Puyravaud JP, Pascal JP, Dufour C (1994) Ecotone structure as an indicator of changing forest-savanna boundaries (Linganamakki Region, Southern India). J Biogeogr 21:581–593

    Article  Google Scholar 

  • Ratter JA, Leitão Filho HF, Argent G, Gibbs PE, Semir J, Shepherd GJ, Tamashiro JY (1988) Floristic composition and community structure of a southern cerrado area in Brazil. Notes R Bot Gard Edinb 45:137–151

    Google Scholar 

  • Roitman I, Felfili JM, Rezende AV (2008) Tree dynamics of a fire-protected cerrados sensu stricto surrounded by forest plantations, over a 13-year period (1991–2004) in Bahia, Brazil. Plant Ecol 197:255–267

    Article  Google Scholar 

  • Rosa R, Lima SC, Assunção LW (1991) Abordagem preliminar das condições climáticas de Uberlândia (MG). Sociedade e Natureza 3:91–108

    Google Scholar 

  • Russell-Smith J, Edwards AC (2006) Seasonality and fire severity in savanna landscapes of monsoonal northern Australia. Int J Wildland Fire 15:307–317

    Article  Google Scholar 

  • Sato MN (2003) Efeito de longo prazo de queimadas prescritas na estrutura da comunidade lenhosa da vegetação do cerrado sensu stricto. Dissertation, Universidade de Brasília, Brasília

  • Schiavini I, Araújo GM (1989) Considerações sobre a vegetação da Reserva Ecológica do Panga (Uberlândia-MG). Sociedade e Natureza (Uberlandia) 1:61–66

    Google Scholar 

  • Silberbauer-Gottsberger I, Eiten G (1983) Fitossociologia de um hectare de cerrado. Brasil Florest 54:55–70

    Google Scholar 

  • Silberbauer-Gottsberger I, Gottsberger GA (1988) A polinização e plantas do cerrado. Rev Bras Biol 48:651–663

    Google Scholar 

  • Silva WR, Sazima M (1995) Hawkmoth pollination in Cereus peruvianus, a columnar cactus of southeastern Brazil. Flora 190:339–343

    Google Scholar 

  • Silva JA, Salomão AN, Gripp A, Leite EJ (1997) Phytosociological survey in Brazilian forest genetic reserve of Caçador. Plant Ecol 133:1–11

    Article  Google Scholar 

  • Soares JJ, Souza MHAO, Lima MIS (2006) Twenty years of post-fire plant succession in a “cerrado”, São Carlos, SP, Brazil. Braz J Biol 66:587–602

    Article  CAS  PubMed  Google Scholar 

  • Steffan-Dewenter I, Tscharntke T (2001) Succession of bee communities on fallows. Ecography 24:83–93

    Article  Google Scholar 

  • Van Nuland ME, Haag EN, Bryant JA, Read QD, Klein RN, Douglas MJ, Gorman CE, Greenwell TD, Busby MW, Collins J, LeRoy JT, Schuchmann G, Schweitzer JA, Bailey JK (2013) Fire promotes pollinator visitation: implications for ameliorating declines of pollination services. PLoS One 8:e79853

    Article  PubMed  PubMed Central  Google Scholar 

  • Wardle DA, Jonsson M (2014) Long-term resilience of above-and belowground ecosystem components among contrasting ecosystems. Ecology 95:1836–1849

    Article  PubMed  Google Scholar 

  • Yachi S, Loreau M (1999) Biodiversity and ecosystem productivity in a fluctuating environment: the insurance hypothesis. PNAS 96:1463–1468

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  • Zamora R (2000) Functional equivalence in plant-animal interactions: ecological and evolutionary consequences. Oikos 88:442–447

    Article  Google Scholar 

Download references

Acknowledgments

We thank Felipe Amorim and Pietro Maruyama for their critical reading and commenting on the manuscript. We thank the three anonymous reviewers for comments and suggestions, which improved the manuscript. We thank the Fundação de Amparo à Pesquisa de Minas Gerais (FAPEMIG) for funding this research.

Author information

Authors and Affiliations

Authors

Corresponding author

Correspondence to Paulo Eugênio Oliveira.

Electronic supplementary material

Below is the link to the electronic supplementary material.

Supplementary material 1 (PDF 154 kb)

Rights and permissions

Reprints and permissions

About this article

Check for updates. Verify currency and authenticity via CrossMark

Cite this article

de Deus, F.F., Oliveira, P.E. Changes in floristic composition and pollination systems in a “Cerrado” community after 20 years of fire suppression. Braz. J. Bot 39, 1051–1063 (2016). https://doi.org/10.1007/s40415-016-0304-9

Download citation

  • Received:

  • Accepted:

  • Published:

  • Issue Date:

  • DOI: https://doi.org/10.1007/s40415-016-0304-9

Keywords

Navigation