Hydrobiologia

, Volume 792, Issue 1, pp 195–207 | Cite as

Factors controlling leaf litter breakdown in Amazonian streams

  • José F. GonçalvesJr.
  • Sheyla R. M. Couceiro
  • Renan S. Rezende
  • Renato T. Martins
  • Bianca M. P. Ottoni-Boldrini
  • Claudimir M. Campos
  • Jeferson O. Silva
  • Neusa Hamada
Primary Research Paper

Abstract

Our objective was to assess the relative importance of leaf litter quality, and the microbial and aquatic invertebrate communities involved in leaf litter breakdown in Amazonian streams. We test the hypothesis that leaf litter quality is the driving force of leaf breakdown rates, rather than the microbial or invertebrate community, independent of stream characteristics. We incubated 3 g of Eucalyptus camaldulensis (EC), Baccharis platypoda, Symphonia globulifera, Mabea speciosa (MS), and Eperua duckeana (ED) leaves in five streams for 75, 56, 46, 26, 14, or 7 days. In all of the streams, leaf litter breakdown was higher for EC and lower in ED. This result may be related to different chemical characteristics among the five studied species. We observed higher frequency of shredders in MS and stream 4, and scrapers in streams 1 and 2. The concentration of ergosterol was higher in MS and lower in EC when adenosine triphosphate differed significantly among streams. Our data indicated that leaf litter quality (chemical and structural components) is a main factor affecting leaf breakdown in Amazonian streams.

Keywords

Chemical composition Decomposition Riparian vegetation Microbial biomass Invertebrates 

Notes

Acknowledgements

JFG and NH received research fellowships (procs. 307479/2011-0, 302957/2014-6, and 306328/2010-0 from the National Council for Scientific and Technological Development (CNPq). RSR received a fellowship from CNPq (proc. 151375/2014-3). RTM received a fellowship from the Programa de Apoio à Fixação de Doutores no Amazonas—FIXAM/AM (FAPEAM). RSR Program in Ecology and Conservation of the UFERSA. We are grateful to FAPEAM and CNPq for financing this study through their support of the DCR project “Effects of the input of anthropogenic sediments on the decomposition of leaves in central Amazonian streams” and the CT-Amazonia project “Anthropogenic sediments in Amazonian streams: impacts on aquatic macroinvertebrates and ecological functioning” (process 575875 2008-9). The CT-Amazônia/CNPq (Proc. 575875/2008-9), Pronex/CNPq/Fapeam—Aquatic insects, CT-Hidro/Climatic Changes/Water Resources/CNPq (Proc. 403949/2013-0), INCT ADAPTA (CNPq/FAPEAM), PROCAD/CAPES 21/2009, and National Program for Support and Development of Botany (Nº: AUX-PE-PNADB 1098/2010) projects supported the invertebrate sampling and laboratory analysis experiments.

Supplementary material

10750_2016_3056_MOESM1_ESM.pdf (2.9 mb)
Fig. S1 Mean values and standard errors of the remaining mass (A; in %/AFDM), shredder frequency (B; in %), scraper frequency (C; in %), density of invertebrates (D; individuals g−1 AFDM), leaf litter, species richness (E; taxa number), biomass of fungal hyphomycetes (F; μg ergosterol g−1 AFDM leaf litter) and total microbial biomass (G; mmoles ATP g−1AFDM leaf litter) over time for the leaf litter of Eucalyptus camaldulensis, Eperua duckeana, Symphonia globulifera, Baccharis platypoda and Mabea speciosa in five Amazon streams. t = time (days), vertical bars = standard error (PDF 2949 kb)
10750_2016_3056_MOESM2_ESM.docx (15 kb)
Table S1 Spearman’s rs correlation between leaf litter breakdown rates and leaf chemical compounds (lignin, cellulose, total polyphenols and tannins) and decomposer communities (aquatic invertebrates and the microbial community) (DOCX 14 kb)

References

  1. Abelho, M., 2001. From litterfall to breakdown in streams: a review. Scientific World Journal 1: 656–680.CrossRefPubMedGoogle Scholar
  2. Abelho, M., 2005. Extraction and quantification of ATP as a measure of microbial biomass. In Graça, M. A. S., F. Bärlocher & M. O. Gessner (eds), Methods to Study Litter Decomposition. Springer, Dordrecht: 223–229.CrossRefGoogle Scholar
  3. Abelho, M., C. Cressa & M. A. S. Graça, 2005. Microbial biomass, respiration, and decomposition of Hura crepitans L. (Euphorbiaceae) leaves in a tropical stream. Biotropica 37: 397–402.CrossRefGoogle Scholar
  4. Abelho, M., M. Moretti, J. Franca & M. Callisto, 2010. Nutrient addition does not enhance leaf decomposition in a Southeastern Brazilian stream (Espinhaco mountain range). Brazilian Journal of Biology 70: 747–754.CrossRefGoogle Scholar
  5. Alvim, E. A. C. C., A. O. Medeiros, R. S. Rezende & J. F. J. Gonçalves, 2015. Leaf breakdown in a natural open tropical stream. Journal of Limnology 74: 228–240.Google Scholar
  6. Ardón, N., L. A. Stallcup & C. M. Pringle, 2006. Does leaf quality mediate the stimulation of leaf breakdown by phosphorus in Neotropical streams? Freshwater Biology 51: 618–633.CrossRefGoogle Scholar
  7. Bärlocher, F. & M. A. S. Graça, 2005. Total Phenolics. In Graça, M. A. S., F. Bärlocher & M. O. Gessner (eds), Methods to Study Litter Decomposition. Springer, Dordrecht: 97–100.CrossRefGoogle Scholar
  8. Boyero, L., R. G. Pearson, D. Dudgeon, M. A. S. Graça, M. O. Gessner, R. Albariño, V. Ferreira, C. M. Yule, A. J. Boulton, M. Arunachalam, M. Callisto, E. Chauvet, A. Ramírez, J. Chará, M. S. Moretti, J. F. J. Gonçalves, J. E. Helson, A. Chará-Serna, A. C. Encalada, J. N. Davies, S. Lamothe, A. Cornejo, A. O. Y. Li, L. M. Buria, V. D. Villanueva, M. C. Zúñiga & C. M. Pringle, 2011a. Global distribution of a key trophic guild contrasts with common latitudinal diversity patterns. Ecology 92: 1839–1848.CrossRefPubMedGoogle Scholar
  9. Boyero, L., R. G. Pearson, M. O. Gessner, L. A. Barmuta, V. Ferreira, M. A. S. Graça, D. Dudgeon, A. J. Boulton, M. Callisto, E. Chauvet, J. E. Helson, A. Bruder, R. J. Albariño, C. M. Yule, M. Arunachalam, J. N. Davies, R. Figueroa, A. S. Flecker, A. Ramírez, R. G. Death, T. Iwata, J. M. Mathooko, C. Mathuriau, J. F. Gonçalves Jr., M. S. Moretti, T. Jinggut, S. Lamothe, C. M’Erimba, L. Ratnarajah, M. H. Schindler, J. Castela, L. M. Buria, A. Cornejo, V. D. Villanueva & D. C. West, 2011b. A global experiment suggests climate warming will not accelerate litter decomposition in streams but might reduce carbon sequestration. Ecology Letters 14: 289–294.CrossRefPubMedGoogle Scholar
  10. Boyero, L., R. G. Pearson, D. Dudgeon, V. Ferreira, M. A. S. Graça, M. O. Gessner, A. J. Boulton, E. Chauvet, C. M. Yule, R. Albariño, A. Ramirez, J. E. Helson, M. Callisto, M. Arunachalam, J. Chará, R. Figueroa, J. M. Mathooko, J. F. J. Gonçalves, M. S. Moretti, A. Chará-Serna, J. N. Davies, A. C. Encalada, S. Lamothe, L. M. Buria, J. Castela, A. Cornejo, A. O. Y. Li, C. M’Erimba, V. D. Villanueva, M. C. Zúñiga, C. M. Swan & L. A. Barmuta, 2012. Global patterns of stream detritivore distribution: implications for biodiversity loss in changing climates. Global Ecology and Biogeography 21: 134–141.CrossRefGoogle Scholar
  11. Bruder, A., M. H. Schindler, M. S. Moretti & M. O. Gessner, 2014. Litter decomposition in a temperate and a tropical stream: the effects of species mixing, litter quality and shredders. Freshwater Biology 59: 438–449.CrossRefGoogle Scholar
  12. Capello, S., M. Marchese & I. Ezcurra de Drago, 2004. Descomposición y colonización por invertebrados de hojas de Salíx humboldtiana en la llanura aluvial del río Paraná medio. Amazoniana 18: 125–143.Google Scholar
  13. Casas, J. J. & M. O. Gessner, 1999. Leaf litter breakdown in a Mediterranean stream characterised by travertine precipitation. Freshwater Biology 41: 781–793.CrossRefGoogle Scholar
  14. Crawley, M. J., 2007. The R Book. Wiley, London.CrossRefGoogle Scholar
  15. Cummins, K. W., R. W. Merritt & P. C. N. Andrade, 2005. The use of invertebrate functional groups to characterize ecosystem attributes in selected streams and rivers in south Brazil. Studies on Neotropical Fauna and Environment 40: 69–89.CrossRefGoogle Scholar
  16. Cummins, K. W., J. R. Sedell, F. J. Swanson, G. W. Minshall, S. G. Fisher, C. E. Cushing, R. C. Petersen & R. L. Vannote, 1983. Organic matter budgets for stream ecosystems: problems in their evaluation. In Barnes, J. R. & G. W. Minshall (eds), Stream Ecology: application and Testing of General Ecological Theory. Plenum Press, New York: 299–353.CrossRefGoogle Scholar
  17. Gessner, M. O., 2005a. Proximate Lignin and Cellulose. In Graça, M. A. S., F. Bärlocher & M. O. Gessner (eds), Methods to Study Litter Decomposition. Springer, Dordrecht: 189–195.CrossRefGoogle Scholar
  18. Gessner, M. O., 2005b. Ergosterol as a measure of fungal biomass. In Graça, M. A. S., F. Bärlocher & M. O. Gessner (eds), Methods to Study Litter Decomposition. Springer, Dordrecht: 115–120.CrossRefGoogle Scholar
  19. Gessner, M. O., E. Chauvet & M. Dobson, 1999. A perspective on leaf litter breakdown in streams. Oikos 85: 377–384.CrossRefGoogle Scholar
  20. Gimenes, K. Z., M. B. Cunha-Santino & I. Bianchini Jr., 2010. Decomposição de matéria orgânica alóctone e autóctone em ecossistemas aquáticos. Oecologia Australis 14: 1036–1073.CrossRefGoogle Scholar
  21. Gonçalves, J. F. J., M. A. S. Graça & M. Callisto, 2006a. Leaf-litter breakdown in 3 streams in temperate, Mediterranean, and tropical Cerrado climates. Journal of the North American Benthological Society 25: 344–355.CrossRefGoogle Scholar
  22. Gonçalves, J. J. F., J. S. França, A. O. Medeiros, C. A. Rosa & M. Callisto, 2006b. Leaf breakdown in a tropical stream. International Review of Hydrobiology 91: 164–177.CrossRefGoogle Scholar
  23. Gonçalves, J. F. J., M. A. S. Graça & M. Callisto, 2007. Litter decomposition in a Cerrado savannah stream is retarded by leaf toughness, low dissolved nutrients and a low density of shredders. Freshwater Biology 52: 1440–1451.CrossRefGoogle Scholar
  24. Gonçalves, J. F. J., R. S. Rezende, N. M. Martins & R. S. Gregorio, 2012a. Leaf breakdown in an Atlantic Rain Forest stream. Austral Ecology 37: 807–815.CrossRefGoogle Scholar
  25. Gonçalves Jr., J. F., R. S. Rezende, J. França & M. Callisto, 2012b. Invertebrate colonisation during leaf processing of native, exotic and artificial detritus in a tropical stream. Marine and Freshwater Research 63: 428–439.CrossRefGoogle Scholar
  26. Gonçalves, J. F. J., R. T. Martins, B. M. P. Ottoni & S. R. M. Couceiro, 2014. Uma visão Sobre a Decomposição Foliar em Sistemas Aquáticos Brasileiros. In Hamada, N., J. L. Nessimian & R. B. Querino (eds), Insetos Aquáticos: Biologia, Ecologia e Taxonomia. Editora INPA, Manaus: 89–116.Google Scholar
  27. Graça, M. A. S., 2001. The role of invertebrates on leaf litter decomposition in streams – a review. International Review of Hydrobiology 86: 383–393.CrossRefGoogle Scholar
  28. Graça, M. A. S., C. Cressa, M. O. Gessner, M. J. Feio, K. A. Callies & C. Barrios, 2001. Food quality, feeding preferences, survival and growth of shredders from temperate and tropical streams. Freshwater Biology 46: 947–957.CrossRefGoogle Scholar
  29. Graça, M. A. S., V. Ferreira, C. Canhoto, A. C. Encalada, F. Guerrero-Bolaño, K. M. Wantzen & L. Boyero, 2015. A conceptual model of litter breakdown in low order streams. International Review of Hydrobiology 100: 1–12.CrossRefGoogle Scholar
  30. Hamada, N. & R. L. M. Ferreira-Keppler, 2012. Guia Ilustrado de Insetos Aquáticos e Semiaquáticos da Reserva Florestal Ducke. Editora da Universidade Federal do Amazonas, Manaus.Google Scholar
  31. Hamada, N., J. L. Nessimian & R. B. Querino, 2014. Insetos Aquáticos na Amazônia Brasileira: Taxonomia, Biologia e Ecologia. Biologia e Ecologia, Manaus.Google Scholar
  32. Irons III, J. G., M. W. Oswood, R. J. Stout & C. M. Pringle, 1994. Latitudinal patterns in leaf litter breakdown: is temperature really important? Freshwater Biology 32: 401–411.CrossRefGoogle Scholar
  33. Landeiro, V. L., N. Hamada & A. S. Melo, 2008. Responses of aquatic invertebrate assemblages and leaf breakdown to macroconsumer exclusion in Amazonian “terra firme” streams. Fundamental and Applied Limnology 172: 49–58.CrossRefGoogle Scholar
  34. Landeiro, V. L., N. Hamada, B. S. Godoy & A. S. Melo, 2010. Effects of litter patch area on macroinvertebrate assemblage structure and leaf breakdown in Central Amazonian streams. Hydrobiologia 649: 355–363.CrossRefGoogle Scholar
  35. Lecerf, A. & J. S. Richardson, 2010. Litter decomposition can detect effects of high and moderate levels of forest disturbance on stream condition. Forest Ecology and Management 259: 2433–2443.CrossRefGoogle Scholar
  36. Ligeiro, R., M. S. Moretti, J. F. Gonçalves & M. Callisto, 2010. What is more important for invertebrate colonization in a stream with low-quality litter inputs: exposure time or leaf species? Hydrobiologia 654: 125–136.CrossRefGoogle Scholar
  37. Martins, R. T., L. S. Silveira & R. G. Alves, 2011. Colonization by oligochaetes (Annelida: clitellata) in decomposing leaves of Eichhornia azurea (SW.) Kunth (Pontederiaceae) in a neotropical lentic system. Annales de Limnologie-International Journal of Limnology 47: 339–346.CrossRefGoogle Scholar
  38. Martins, R. T., A. S. Melo, J. F. G. Júnior & N. Hamada, 2015. Leaf-litter breakdown in urban streams of Central Amazonia: direct and indirect effects of physical, chemical, and biological factors. Freshwater Science 34: 716–726.CrossRefGoogle Scholar
  39. Meentemeyer, V., 1978. Macroclimate and lignin control of litter decomposition rates. Ecology 59: 465–472.CrossRefGoogle Scholar
  40. Mendonça, F. P., W. E. Magnusson & J. Zuanon, 2005. Relationships between habitat characteristics and fish assemblages in small streams of Central Amazonia. Copeia 4: 751–764.CrossRefGoogle Scholar
  41. Merritt, R. W., K. W. Cummins & M. B. Berg, 2008. An Introduction to the Aquatic Insects of North America, 4th ed. Kendall/Hunt, Dubuque.Google Scholar
  42. Moretti, M., J. J. F. Gonçalves & M. Callisto, 2007. Leaf breakdown in two tropical streams: differences between single and mixed species packs. Limnologica 37: 250–258.CrossRefGoogle Scholar
  43. Moulton, T. P., S. A. P. Magalhães-Fraga, E. F. Brito & F. A. Barbosa, 2010. Macroconsumers are more important than specialist macroinvertebrate shredders in leaf processing in urban forest streams of Rio de Janeiro, Brazil. Hydrobiologia 638: 55–66.CrossRefGoogle Scholar
  44. Pérez, G. P., 1988. Guía para el Studio de Los Macroinvertebrados Acuáticos del Departamento de Antioquia. Editorial Presencia Ltda, Bogotá.Google Scholar
  45. Petersen, R. C. & K. W. Cummins, 1974. Leaf processing in a woodland stream. Freshwater Biology 4: 343–368.CrossRefGoogle Scholar
  46. Rezende, R. S., J. F. Gonçalves Jr. & M. M. Petrucio, 2010. Leaf breakdown and invertebrate colonization of Eucalyptus grandis (Myrtaceae) and Hirtella glandulosa (Chrysobalanaceae) in two Neotropical lakes. Acta Limnologica Brasiliensia 22: 23–34.CrossRefGoogle Scholar
  47. Rezende, R. S., M. M. Petrucio & J. F. Gonçalves Jr., 2014. The Effects of Spatial Scale on Breakdown of Leaves in a Tropical Watershed. PLoS ONE 9: e97072.CrossRefPubMedPubMedCentralGoogle Scholar
  48. Rezende, R. D. S., M. A. S. Graça, A. M. Santos, A. O. Medeiros, P. F. Santos, Y. R. Nunes & J. F. G. Junior, 2016. Organic matter dynamics in a tropical gallery forest in a grassland landscape. Biotropica 1: 301–310.CrossRefGoogle Scholar
  49. Ribeiro, J. E. L. S., M. J. G. Hopkins, A. Vicentini, C. A. Sothers, M. A. S. Costa, J. M. De Brito, M. A. D. De Souza, L. H. P. Martins, L. G. Lohmann, P. A. C. L. Assunção, E. C. Pereira, C. F. Da Silva, M. Mesquita & L. C. Procópio, 1999. Flora da Reserva Ducke: Guia de Identificação das Plantas Vasculares de uma Floresta de Terra Firme na Amazônia Central. Editora INPA, Manaus.Google Scholar
  50. Rousk, J., E. Baath, P. C. Brookes, C. L. Lauber, C. Lozupone, J. G. Caporaso, R. Knight & N. Fierer, 2010. Soil bacterial and fungal communities across a pH gradient in an arable soil. The International Society for Microbial Ecology Journal 4: 1340–1351.Google Scholar
  51. Tank, J. L., E. J. Rosi-Marshall, N. A. Griffiths, S. A. Entrekin & M. L. Stephen, 2010. A review of allochthonous organic matter dynamics and metabolism in streams. Journal of the North American Benthological Society 29: 118–146.CrossRefGoogle Scholar
  52. The R Core Team, 2013. R: a Language and Environment for Statistical Computing. R Foundation for Statistical Computing, Vienna.Google Scholar
  53. Tonin, A. M., L. U. Hepp, R. M. Restello & J. F. Gonçalves, 2014. Understanding of colonization and breakdown of leaves by invertebrates in a tropical stream is enhanced by using biomass as well as count data. Hydrobiologia 740: 79–88.CrossRefGoogle Scholar
  54. Wallace, J. B., S. L. Eggert, J. L. Meyer & J. R. Webster, 1997. Multiple trophic levels of a forest stream linked to terrestrial litter inputs. Science 277: 102–104.CrossRefGoogle Scholar
  55. Webster, J. R. & J. L. Meyer, 1997. Organic matter budgets for stream a synthesis. In: Webster, J. R. & J. L. Meyer. Stream organic matter budgets. Journal of the North American Benthological Society 16: 3–161.Google Scholar

Copyright information

© Springer International Publishing Switzerland 2016

Authors and Affiliations

  • José F. GonçalvesJr.
    • 1
  • Sheyla R. M. Couceiro
    • 2
  • Renan S. Rezende
    • 3
    • 4
  • Renato T. Martins
    • 3
  • Bianca M. P. Ottoni-Boldrini
    • 5
  • Claudimir M. Campos
    • 3
  • Jeferson O. Silva
    • 3
  • Neusa Hamada
    • 3
  1. 1.Laboratório de Limnologia, Departamento de Ecologia, IBUniversidade de BrasíliaBrasíliaBrazil
  2. 2.Laboratório de Ecologia e Taxonomia de Invertebrados Aquáticos, Instituto de Ciências e Tecnologia das ÁguasUniversidade Federal do Oeste do ParáSantarémBrazil
  3. 3.Programa de Pós-Graduação em Entomologia, Coordenação de BiodiversidadeInstituto Nacional de Pesquisas da Amazônia - INPAManausBrazil
  4. 4.Programa de Pós-Graduação em Ecologia e ConservaçãoUniversidade Federal Rural do Semi-Árido-UFERSAMossoróBrazil
  5. 5.Colégio de Aplicação, Centro de EducaçãoUniversidade Federal de RoraimaBoa VistaBrazil

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