Skip to main content

Advertisement

Log in

Breakdown of green and senescent leaves in Amazonian streams: a case study

  • Research paper
  • Published:
Limnology Aims and scope Submit manuscript

Abstract

Allochthonous organic matter in low-order streams is, in general, mainly composed of senescent leaves. However, in tropical streams green leaves can represent an important source of energy. The present study evaluated the decomposition of green and senescent leaves in Amazonian streams using leaves of three plant species: Inga stipularis D.C. 1876, Tococa guianensis Aubl. 1775 and Vochysia ferruginea Mart. 1826. The leaves were incubated for 120 days in four streams in the municipality of Santarém in western Pará State, Brazil. Senescent leaves were collected using nylon nets suspended 1 m above the ground, while green leaves were collected manually, directly from the trees. Green leaves exhibited better nutritional status: higher values for nitrogen and phosphate and lower values for carbon. Toughness and percentages of tannin and lignin of the green and senescent leaves varied among the studied species. Mass loss of green leaves was ~ 3.5 times higher than that of senescent leaves after 120 days. Higher values of phosphate and nitrogen and lower values of carbon, tannin, and lignin in green leaves were fundamental in explaining the difference in decomposition between green and senescent leaves. These differences reinforce the importance of understanding the role of green leaves in aquatic environments.

This is a preview of subscription content, log in via an institution to check access.

Access this article

Subscribe and save

Springer+ Basic
$34.99 /Month
  • Get 10 units per month
  • Download Article/Chapter or eBook
  • 1 Unit = 1 Article or 1 Chapter
  • Cancel anytime
Subscribe now

Buy Now

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

Explore related subjects

Discover the latest articles and news from researchers in related subjects, suggested using machine learning.

References

  • Abelho M, Graça MAS (2006) Effects of nutrient enrichment on decomposition and fungal colonization of sweet chestnut leaves in an Iberian stream (Central Portugal). Hydrobiologia 560:239–247

    CAS  Google Scholar 

  • Aoyama S, Reyes TH, Guglielminetti L, Lu Y, Morita Y, Sato T, Yamaguchi J (2014) Ubiquitin ligase ATL31 functions in leaf senescence in response to the balance between atmospheric CO2 and nitrogen availability in Arabidopsis. Plant Cell Physiol 55:293–305

    CAS  PubMed  PubMed Central  Google Scholar 

  • Austin AT, Ballare CL (2010) Dual role of lignin in plant litter decomposition in terrestrial ecosystems. Proc Natl Acad Sci 107:4618–4622

    CAS  PubMed  Google Scholar 

  • Bastian M, Boyero L, Jackes B, Pearson RG (2007) Leaf litter diversity and shredder preferences in an Australian tropical rainforest stream. J Trop Ecol 23:219–229

    Google Scholar 

  • Benson LJ, Pearson RG (1993) Litter inputs to a tropical Australian rainforest stream. Aust J Ecol 18:377–383

    Google Scholar 

  • Campbell IC, James KR, Hart BT, Devereaux A (1992) Allochthonous coarse particulate organic material in forest and pasture reaches of two south-eastern Australian streams: II. Litter processing. Freshw Biol 27:353–365

    Google Scholar 

  • Canhoto C, Graça MAS (1996) Decomposition of Eucalyptus globulus leaves and three native leaf species (Alnus glutinosa, Castanea sativa and Quercus faginea) in a Portuguese low order stream. Hydrobiologia 333:79–85

    CAS  Google Scholar 

  • Caño-Delgado A, Penfield S, Smith C, Catley M, Bevan M (2003) Reduced cellulose synthesis invokes lignification and defense responses in Arabidopsis thaliana. Plant J 34:351–362

    PubMed  Google Scholar 

  • Chen D, Wang S, Xiong B, Cao B, Deng X (2015) Carbon/nitrogen imbalance associated with drought-induced leaf senescence in Sorghum bicolor. PLoS ONE 10:e0137026

    PubMed  PubMed Central  Google Scholar 

  • Cillero C, Pardo I, López ES (1999) Comparisons of riparian vs over stream trap location in the estimation of vertical litterfall inputs. Hydrobiologia 416:171–179

    CAS  Google Scholar 

  • Crowl TA, Welsh V, Heartsill-Scalley T, Covich AP (2006) Effects of different types of conditioning on rates of leaf-litter shredding by Xiphocaris elongata, a Neotropical freshwater shrimp. J N Am Benthol Soc 25:198–208

    Google Scholar 

  • Delgado GR, Wantzen KM, Tolosa MB (2006) Leaf-litter decomposition in an Amazonian floodplain stream: effects of seasonal hydrological changes. J N Am Benthol Soc 25:233–249

    Google Scholar 

  • Ferreira LV, Prance GT (1998) Species richness and floristic composition in four hectares in the Jau National Park in upland forests in Central Amazonia. Biodivers Conserv 7:1349–1364

    Google Scholar 

  • Fonte SJ, Schowalter TD (2004) Decomposition of greenfall vs. senescent foliage in a Tropical forest ecosystem in Puerto Rico. Biotropica 36:474–482

    Google Scholar 

  • Friberg N, Jacobsen D (1994) Feeding plasticity of two detritivore-shredders. Freshw Biol 32:133–142

    Google Scholar 

  • Gan S, Amasino RM (1997) Making sense of senescence (molecular genetic regulation and manipulation of leaf senescence). Plant Physiol 113:313–319

    CAS  PubMed  PubMed Central  Google Scholar 

  • Gessner MO (1991) Differences in processing dynamics of fresh and dried leaf litter in a stream ecosystem. Freshw Biol 26:387–398

    CAS  Google Scholar 

  • Gessner MO (2005) Proximate lignin and cellulose. In: Graça MAS, Bärlocher F, Gessner MO (eds) Methods to study litter decomposition. Springer Netherlands, Amsterdam, pp 115–120. https://doi.org/10.1007/1-4020-3466-0

  • Gobbo-Neto L, Lopes NP (2007) Plantas medicinais: fatores de influência no conteúdo de metabólitos secundários. Quim Nova 30:374–381

    CAS  Google Scholar 

  • Gonçalves JF, França JS, Medeiros AO, Rosa CA, Callisto M (2006) Leaf breakdown in a tropical stream. Int Rev Hydrobiol 91:164–177

    Google Scholar 

  • Gonçalves JF, Couceiro SRM, Rezende RS, Martins RT, Ottoni-Boldrini BMP, Campos CM, Silva JO, Hamada N (2016) Factors controlling leaf litter breakdown in Amazonian streams. Hydrobiologia 792:195–207

    Google Scholar 

  • Gonçalves JF, Martins RT, Ottoni BMP, Couceiro SRM (2014) Uma visão sobre a decomposição foliar em sistemas aquáticos brasileiros. In: Hamada N, Nessimian JL, Querino RB (eds) Insetos Aquáticos na Amazônia brasileira: taxonomia, biologia e ecologia. Editora do INPA, pp 89–116

  • Gonçalves JF, Rezende RS, Martins NM, Gregório RS (2012) Leaf breakdown in an Atlantic Rain Forest stream. Austral Ecol 37:807–815

    Google Scholar 

  • Graça MAS (2001) The role of invertebrates on leaf litter decomposition in streams—a review. Int Rev Hydrobiol 86:383–393

    Google Scholar 

  • Graça MAS, Canhoto C (2006) Leaf litter processing in low order streams. Limnetica 25:1–10

    Google Scholar 

  • Graça MAS, Bärlocher F, Gessner MO (2005) Methods to study litter decomposition. Springer Netherlands, Amsterdam, pp 115–120. https://doi.org/10.1007/1-4020-3466-0

  • Graça MAS, Ferreira V, Canhoto C, Encalada AC, Guerrero-Bolaño F, Wantzen KM, Boyero L (2015) A conceptual model of litter breakdown in low order streams. Int Rev Hydrobiol 100:1–12

    Google Scholar 

  • Harborne JB (1997) Biochemical plant ecology. In: Dey PM, Harborne JB (eds) Plant biochemistry. Academic Press, New York, pp 503–516. https://doi.org/10.1016/B978-0-12-214674-9.X5000-0

  • Hayashi SN, Vieira ICG, Carvalho CJR, Davidson E (2012) Linking nitrogen and phosphorus dynamics in litter production and decomposition during secondary forest succession in the eastern Amazon. Bol Mus Para Emílio Goeldi Cienc Nat 7:283–295

    Google Scholar 

  • Hegarty EE (1991) Leaf litter production by lianes and trees in a sub-tropical Australian rain forest. J Trop Ecol 7:201–214

    Google Scholar 

  • Henriques LMP, Wunderle JM Jr, Oren DC, Willig MR (2008) Efeitos da exploração madeireira de baixo impacto sobre uma comunidade de aves de sub-bosque na Floresta Nacional do Tapajós, Pará, Brasil. Acta Amaz 38:267–290

    Google Scholar 

  • Hodges DM, Forney CF (2000) The effects of ethylene, depressed oxygen and elevated carbon dioxide on antioxidant profiles of senescing spinach leaves. J Exp Bot 51:645–655

    CAS  PubMed  Google Scholar 

  • Hoorens B, Aerts R, Stroetenga M (2003) Does initial litter chemistry explain litter mixture effects on decomposition? Oecologia 137:578–586

    PubMed  Google Scholar 

  • Kao WY, Tsai HC, Shih CN, Tsai TT, Handley LL (2002) Nutrient contents, d13C and d15N during leaf senescence in the mangrove, Kandelia candel (L.) Druce. Bot Bull Acad Sinica 43:277–282

    CAS  Google Scholar 

  • Kochi K, Kagaya T (2005) Green leaves enhance the growth and development of a stream macroinvertebrate shredder when senescent leaves are available. Freshw Biol 50:656–667

    Google Scholar 

  • Kochi K, Yanai S (2006) Shredder colonization and decomposition of green and senescent leaves during summer in a headwater stream in northern Japan. Ecol Res 21:544–550

    Google Scholar 

  • Kochi K, Yanai S, Nagasaka A (2004) Energy input from a riparian forest into a headwater stream in Hokkaido, Japan. Arch Hydrobiol 160:231–246

    Google Scholar 

  • Kochi K, Asaeda T, Chibana T, Fujino T (2009) Physical factors affecting the distribution of leaf litter patches in streams: comparison of green and senescent leaves in a step-pool streambed. Hydrobiologia 628:191–201

    Google Scholar 

  • Kochi K, Kagaya T, Kusumoto D (2010a) Does mixing of senescent and green leaves result in nonadditive effects on leaf decomposition? J N Am Benthol Soc 29:454–464

    Google Scholar 

  • Kochi K, Mishima Y, Nagasaka A (2010b) Lateral input of particulate organic matter from bank slopes surpasses direct litter fall in the uppermost reaches of a headwater stream in Hokkaido, Japan. Limnology 11:77–84

    CAS  Google Scholar 

  • Kottek M, Grieser J, Beck C, Rudolf B, Rubel F (2006) World map of the Köppen-Geiger climate classification updated. Meteorol Z 15:259–263

    Google Scholar 

  • Landeiro VL, Hamada N, Godoy BS, Melo AS (2010) Effects of litter patch area on macroinvertebrate assemblage structure and leaf breakdown in Central Amazonian streams. Hydrobiologia 649:355–363

    Google Scholar 

  • Leff LG, Vaun McArthur J (1990) Effect of nutrient content on leaf decomposition in a coastal plain stream: a comparison of green and senescent leaves. J Freshw Ecol 5:269–277

    CAS  Google Scholar 

  • Lopes MP, Martins RT, Silveira LS, Alves RG (2015) The leaf breakdown of Picramnia sellowii (Picramniales: Picramniaceae) as index of anthropic disturbances in tropical streams. Braz J Biol 75:846–853

    CAS  PubMed  Google Scholar 

  • López ES, Pardo I, Felpeto N (2001) Seasonal differences in green leaf breakdown and nutrient content of deciduous and evergreen tree species and grass in a granitic headwater stream. Hydrobiologia 464:51–61

    Google Scholar 

  • Magnusson WE, Lima AP, Albernaz ALKM, Sanaiotti TM, Guillaumet JL (2008) Composição florística e cobertura vegetal das savanas na região de Alter do Chão, Santarém—PA. Rev Bras Bot 31:165–177

    Google Scholar 

  • Maloney DC, Lamberti GA (1995) Rapid decomposition of summer-input leaves in a Northern Michigan stream. Am Midl Nat 133:184–195

    Google Scholar 

  • Marchin R, Zeng H, Hoffmann W (2010) Drought-deciduous behavior reduces nutrient losses from temperate deciduous trees under severe drought. Oecologia 163:845–854

    PubMed  Google Scholar 

  • Martins RT, Melo AS, Gonçalves JF, Hamada N (2015) Leaf-litter breakdown in urban streams of Central Amazonia: direct and indirect effects of physical, chemical, and biological factors. Freshw Sci 34:716–726

    Google Scholar 

  • Martins RT, Melo AS, Gonçalves JF, Campos CM, Hamada N (2017) Effects of climate change on leaf breakdown by microorganisms and the shredder Phylloicus elektoros (Trichoptera: Calamoceratidae). Hydrobiologia 789:31–44

    CAS  Google Scholar 

  • Melack JM, Forsberg BR (2001) Biogeochemistry of Amazon floodplain lakes and associated wetlands (pp. 235–274). In: McClain ME, Victoria RL, Richey JE (eds) The biogeochemistry of the Amazon Basin. Oxford University Press, Oxford, p 365

    Google Scholar 

  • Michelangeli FA (2003) Ant protection against herbivory in three species of Tococa (Melastomataceae) occupying different environments. Biotropica 35:181–188

    Google Scholar 

  • Michelangeli FA (2005) Tococa (Melastomataceae). Flora Neotrop 23:1–114

    Google Scholar 

  • Miller HG (1984) Dynamics of nutrient cycling in plantations ecosystems. In: Bowen GD, Nambiar EKS (eds) Nutrition of Forest Trees in Plantations. Academic Press, London, pp 53–78

    Google Scholar 

  • Petersen RC, Cummins KW (1974) Leaf processing in a woodland stream. Freshw Biol 4:343–368

    Google Scholar 

  • R Core Team (2018) R: a language and environment for statistical computing. R Foundation for Statistical Computing, Vienna, Austria. https://www.R-project.org/. Accessed 1 July 2019

  • Romero R, Martins AB (2002) Melastomataceae do Parque Nacional da Serra da Canastra, Minas Gerais, Brasil. Rev Bras Bot 25:19–24

    Google Scholar 

  • Rosemond AD, Pringle CM, Ramírez A, Paul MJ, Meyer JL (2002) Landscape variation in phosphorus concentration and effects on detritus-based tropical streams. Limnol Oceanogr 47:278–289

    CAS  Google Scholar 

  • Shay PE, Peter Constabel C, Trofymow JA (2017) Evidence for the role and fate of water-insoluble condensed tannins in the short-term reduction of carbon loss during litter decay. Biogeochemistry 137:127–141

    Google Scholar 

  • Stout RJ, Taft WH, Merritt RW (1985) Patterns of macroinvertebrate colonization on fresh and senescent alder leaves in two Michigan streams. Freshw Biol 15:573–580

    Google Scholar 

  • Suberkropp K (1998) Effect of dissolved nutrients on two aquatic hyphomycetes growing on leaf litter. Mycol Res 102:998–1002

    CAS  Google Scholar 

  • Suberkropp K, Chauvet E (1995) Regulation of leaf breakdown by fungi in streams: influences of water chemistry. Ecology 76:1433–1445

    Google Scholar 

  • Taylor BR, Bärlocher F (1996) Variable effects of air-drying on leaching losses from tree leaf litter. Hydrobiologia 325:173–182

    CAS  Google Scholar 

  • Tonin AM, Gonçalves JF, Bambi P, Couceiro SRM, Feitoza LAM, Fontana LE, Boyero L (2017) Plant litter dynamics in the forest-stream interface: precipitation is a major control across tropical biomes. Sci Rep. https://doi.org/10.1038/s41598-017-10576-8

    Article  PubMed  PubMed Central  Google Scholar 

  • Vanholme R, Demedts B, Morreel K, Ralph J, Boerjan W (2010) Lignin biosynthesis and structure. Plant Physiol 153:895–905

    CAS  PubMed  PubMed Central  Google Scholar 

  • Vannote RL, Minshall GW, Cummins KW, Sedell JR, Cushing CE (1980) The river continuum concept. Can J Fish Aquat Sci 37:130–137

    Google Scholar 

  • Vaun McArthur J, Leff LG, Kovacic DA, Jaroscak J (1986) Green leaf decomposition in Coastal Plain streams. J Freshw Ecol 3:553–558

    Google Scholar 

  • Wantzen KM, Wagner R (2006) Detritus processing by invertebrate shredders: a neotropical-temperate comparison. J N Am Benthol Soc 25:216–232

    Google Scholar 

  • Webster JR, Benfield EF (1986) Vascular plant breakdown in freshwater ecosystems. Annu Rev Ecol and Syst 17:567–594

    Google Scholar 

Download references

Acknowledgements

The authors thank Universidade Federal do Oeste do Pará—UFOPA for logistic support and CAPES—Coordination for the Improvement of Higher Education Personnel. MA received a master scholarship from Coordenação de Aperfeiçoamento de Pessoal de Nível Superior (CAPES). They are grateful to CNPq for financial support through the project “Trophic classification of the aquatic insects of Amazonian streams” (process 477187/2012-9). RTM was supported by Programa de Apoio à Fixação de Doutores no Amazonas–FIXAM/AM (FAPEAM) and INCT ADAPTA-II funded by CNPq–Brazilian National Research Council (465540/2014-7) and FAPEAM–Amazonas State Research Foundation (062.1187/2017).

Author information

Authors and Affiliations

Authors

Corresponding author

Correspondence to Marcelo Alves.

Additional information

Publisher's Note

Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.

Handling Editor: Luz Boyero.

Rights and permissions

Reprints and permissions

About this article

Check for updates. Verify currency and authenticity via CrossMark

Cite this article

Alves, M., Martins, R.T. & Couceiro, S.R.M. Breakdown of green and senescent leaves in Amazonian streams: a case study. Limnology 22, 27–34 (2021). https://doi.org/10.1007/s10201-020-00626-y

Download citation

  • Received:

  • Accepted:

  • Published:

  • Issue Date:

  • DOI: https://doi.org/10.1007/s10201-020-00626-y

Keywords