Changes in Amazonian Forest Biomass, Dynamics, and Composition, 1980–2002

© 2009 by the American Geophysical Union. All rights reserved. Long-term, on-the-ground monitoring of forest plots distributed across Amazonia provides a powerful means to quantify stocks and fluxes of biomass and biodiversity. Here we examine the evidence for concerted changes in the structure, dynamics, and functional composition of old-growth Amazonian forests over recent decades. Mature forests have, as a whole, gained biomass and undergone accelerated growth and dynamics, but questions remain as to the long-term persistence of these changes. Because forest growth on average exceeds mortality, intact Amazonian forests have been functioning as a carbon sink. We estimate a net biomass increase in trees > 10 cm diameter of 0.62 ± 0.23 t C ha -1 a -1 through the late twentieth century. If representative of the wider forest landscape, this translates into a sink in South American old-growth forest of at least 0.49 ± 0.18 Pg C a -1 . If other biomass and necromass components also increased proportionally, the estimated South American old-growth forest sink is 0.79 ± 0.29 Pg C a -1 , before allowing for possible gains in soil carbon. If tropical forests elsewhere are behaving similarly, the old-growth biomass forest sink would be 1.60 ± 0.58 Pg C a -1 . This bottom-up estimate of the carbon balance of tropical forests is preliminary, pending syntheses of detailed biometric studies across the other tropical continents. There is also some evidence for recent changes in the functional composition (biodiversity) of Amazonian forest, but the evidence is less comprehensive than that for changes in structure and dynamics. The most likely driver(s) of changes are recent increases in the supply of resources such as atmospheric carbon dioxide, which would increase net primary productivity, increasing tree growth and recruitment, and, in turn, mortality. In the future the growth response of remaining undisturbed Amazonian forests is likely to saturate, and there is a risk of these ecosystems transitioning from sink to source driven by higher respiration (temperature), higher mortality (drought), or compositional change (functional shifts toward lighterwooded plants). Even a modest switch from carbon sink to source for Amazonian forests would impact global climate, biodiversity, and human welfare, while the documented acceleration of tree growth and mortality may already be affecting the interactions of thousands of plant and millions of animal species.

[1]  J. Chambers,et al.  Tree allometry and improved estimation of carbon stocks and balance in tropical forests , 2005, Oecologia.

[2]  Susan E. Trumbore,et al.  Respiration from a tropical forest ecosystem: partitioning of sources and low carbon use efficiency , 2004 .

[3]  D. Clark ARE TROPICAL FORESTS AN IMPORTANT CARBON SINK? REANALYSIS OF THE LONG-TERM PLOT DATA , 2002 .

[4]  Oliver L. Phillips,et al.  Growth and wood density predict tree mortality in Amazon forests , 2008 .

[5]  O. Phillips,et al.  Tropical Forests and Global Atmospheric Change , 2005 .

[6]  M. G. Ryan,et al.  Wood CO2 efflux in a primary tropical rain forest , 2006 .

[7]  Y. Malhi,et al.  Tropical forests and atmospheric carbon dioxide. , 2000, Trends in ecology & evolution.

[8]  S. Wright,et al.  Tropical forests in a changing environment. , 2005, Trends in ecology & evolution.

[9]  Patrick M. Crill,et al.  A source of methane from upland forests in the Brazilian Amazon , 2006 .

[10]  William F. Laurance,et al.  Amazonian Tree Mortality during the 1997 El Niño Drought , 2000 .

[11]  F. Woodward,et al.  Global response of terrestrial ecosystem structure and function to CO2 and climate change: results from six dynamic global vegetation models , 2001 .

[12]  M. Ball,et al.  Leaf respiration of snow gum in the light and dark. Interactions between temperature and irradiance. , 2000, Plant physiology.

[13]  Christian Wirth,et al.  Seasonal and annual variations in the photosynthetic productivity and carbon balance of a central Siberian pine forest , 2002 .

[14]  Eric A. Davidson,et al.  The effects of partial throughfall exclusion on canopy processes, aboveground production, and biogeochemistry of an Amazon forest , 2002 .

[15]  J. Chambers,et al.  Regional ecosystem structure and function: ecological insights from remote sensing of tropical forests. , 2007, Trends in ecology & evolution.

[16]  M. Williams,et al.  A comparison of methods for converting rhizotron root length measurements into estimates of root mass production per unit ground area , 2007, Plant and Soil.

[17]  A. Di Fiore,et al.  Increasing biomass in Amazonian forest plots. , 2004, Philosophical transactions of the Royal Society of London. Series B, Biological sciences.

[18]  M. G. Ryan,et al.  Carbon allocation in forest ecosystems , 2007 .

[19]  D. Bird,et al.  Effects of syn-pandemic fire reduction and reforestation in the tropical Americas on atmospheric CO2 during European conquest , 2008 .

[20]  Eileen H. Helmer,et al.  Root biomass allocation in the world's upland forests , 1997, Oecologia.

[21]  Luiz Antonio Martinelli,et al.  Influence of soil texture on carbon dynamics and storage potential in tropical forest soils of Amazonia , 2003 .

[22]  W. Silver,et al.  Fine root dynamics and trace gas fluxes in two lowland tropical forest soils , 2005 .

[23]  James H. Brown,et al.  A general model for the structure and allometry of plant vascular systems , 1999, Nature.

[24]  Robert K. Colwell,et al.  Species Loss and Aboveground Carbon Storage in a Tropical Forest , 2005, Science.

[25]  P. Crutzen Geology of mankind , 2002, Nature.

[26]  C. Körner,et al.  In deep shade, elevated CO2 increases the vigor of tropical climbing plants , 2002 .

[27]  L. Hess,et al.  Outgassing from Amazonian rivers and wetlands as a large tropical source of atmospheric CO2 , 2002, Nature.

[28]  Joaquim dos Santos,et al.  Biomassa da parte aérea da vegetação da Floresta Tropical úmida de terra-firme da Amazônia Brasileira , 1998 .

[29]  R. Condit,et al.  Pervasive alteration of tree communities in undisturbed Amazonian forests , 2004, Nature.

[30]  Phillips,et al.  Changes in the carbon balance of tropical forests: evidence from long-term plots , 1998, Science.

[31]  T. Vesala,et al.  On the separation of net ecosystem exchange into assimilation and ecosystem respiration: review and improved algorithm , 2005 .

[32]  Luiz Antonio Martinelli,et al.  Forest structure and carbon dynamics in Amazonian tropical rain forests , 2004, Oecologia.

[33]  Archaeology: Progress and pitfalls in radiocarbon dating (Reply) , 2006, Nature.

[34]  Suan Chin Wong,et al.  A simple calibrated model of Amazon rainforest productivity based on leaf biochemical properties , 1995 .

[35]  R. B. Jackson,et al.  A global analysis of root distributions for terrestrial biomes , 1996, Oecologia.

[36]  G. Pétron,et al.  Biogenic VOC emissions from forested Amazonian landscapes , 2004 .

[37]  S. Patiño,et al.  Ecophysiology of Forest and Savanna Vegetation , 2013 .

[38]  D. Metcalfe,et al.  The fate of assimilated carbon during drought: impacts on respiration in Amazon rainforests , 2008, Philosophical Transactions of the Royal Society B: Biological Sciences.

[39]  M. Keller,et al.  Coarse woody debris in undisturbed and logged forests in the eastern Brazilian Amazon , 2004 .

[40]  Jeffrey Q. Chambers,et al.  MEASURING NET PRIMARY PRODUCTION IN FORESTS: CONCEPTS AND FIELD METHODS , 2001 .

[41]  G. Yohe,et al.  A globally coherent fingerprint of climate change impacts across natural systems , 2003, Nature.

[42]  R. Betts,et al.  Acceleration of global warming due to carbon-cycle feedbacks in a coupled climate model , 2000, Nature.

[43]  Kaoru Kitajima,et al.  Cloud cover limits net CO2 uptake and growth of a rainforest tree during tropical rainy seasons , 2003, Proceedings of the National Academy of Sciences of the United States of America.

[44]  Simon L Lewis,et al.  Tropical forests and the changing earth system , 2006, Philosophical Transactions of the Royal Society B: Biological Sciences.

[45]  Hudson Silva,et al.  Necromass production: studies in undisturbed and logged Amazon forests. , 2008, Ecological applications : a publication of the Ecological Society of America.

[46]  Stan D. Wullschleger,et al.  Net primary productivity of a CO2-enriched deciduous forest and the implications for carbon storage , 2002 .

[47]  P. Meir,et al.  Scaling relationships for woody tissue respiration in two tropical rain forests , 2002 .

[48]  Luiz Antonio Martinelli,et al.  Slow growth rates of Amazonian trees: consequences for carbon cycling. , 2005, Proceedings of the National Academy of Sciences of the United States of America.

[49]  G. Farquhar,et al.  The CO 2 Dependence of Photosynthesis, Plant Growth Responses to Elevated Atmospheric CO 2 Concentrations and Their Interaction with Soil Nutrient Status. I. General Principles and Forest Ecosystems , 1996 .

[50]  Michael W. Palace,et al.  CARBON BALANCE AND VEGETATION DYNAMICS IN AN OLD-GROWTH AMAZONIAN FOREST , 2004 .

[51]  Y. Malhi,et al.  The response of an Eastern Amazonian rain forest to drought stress: results and modelling analyses from a throughfall exclusion experiment , 2007 .

[52]  E. Baggs,et al.  Partitioning the components of soil respiration: a research challenge , 2006, Plant and Soil.

[53]  C. Körner Through enhanced tree dynamics carbon dioxide enrichment may cause tropical forests to lose carbon. , 2004, Philosophical transactions of the Royal Society of London. Series B, Biological sciences.

[54]  O. Phillips,et al.  The RAINFOR database: monitoring forest biomass and dynamics , 2007 .

[55]  O. Phillips,et al.  Dynamics and species richness of tropical rain forests. , 1994, Proceedings of the National Academy of Sciences of the United States of America.

[56]  A. Huete,et al.  Amazon rainforests green‐up with sunlight in dry season , 2006 .

[57]  Richard Condit,et al.  Assessing Evidence for a Pervasive Alteration in Tropical Tree Communities , 2008, PLoS biology.

[58]  J. Terborgh,et al.  Concerted changes in tropical forest structure and dynamics: evidence from 50 South American long-term plots. , 2004, Philosophical transactions of the Royal Society of London. Series B, Biological sciences.

[59]  Eric A. Davidson,et al.  Recuperation of nitrogen cycling in Amazonian forests following agricultural abandonment , 2007, Nature.

[60]  M. Silman,et al.  Holocene fire and occupation in Amazonia: records from two lake districts , 2007, Philosophical Transactions of the Royal Society B: Biological Sciences.

[61]  Gregory P. Asner,et al.  Necromass in undisturbed and logged forests in the Brazilian Amazon , 2007 .

[62]  Susan E. Trumbore,et al.  Carbon sink for a century , 2001, Nature.

[63]  R. Betts,et al.  Amazonian forest dieback under climate-carbon cycle projections for the 21st century , 2004 .

[64]  M. G. Ryan,et al.  Foliar and Ecosystem Respiration in an Old-growth Tropical Rain Forest , 2022 .

[65]  U. Salzmann,et al.  The Dahomey Gap: an abrupt climatically induced rain forest fragmentation in West Africa during the late Holocene , 2005 .

[66]  William F. Laurance,et al.  Dynamics of carbon, biomass, and structure in two Amazonian forests , 2008 .

[67]  O. Phillips,et al.  Low stocks of coarse woody debris in a southwest Amazonian forest , 2007, Oecologia.

[68]  Richard Condit,et al.  Error propagation and scaling for tropical forest biomass estimates. , 2004, Philosophical transactions of the Royal Society of London. Series B, Biological sciences.

[69]  Hirofumi Hashimoto,et al.  Modeling the interannual variability and trends in gross and net primary productivity of tropical forests from 1982 to 1999 , 2005 .

[70]  J. Lelieveld,et al.  Isoprene and monoterpene fluxes from Central Amazonian rainforest inferred from tower-based and airborne measurements, and implications on the atmospheric chemistry and the local carbon budget , 2007 .

[71]  P. Camargo,et al.  Ecophysiology of Forest and Savanna Vegetation , 2013 .

[72]  Javier Tomasella,et al.  Export of organic carbon in run‐off from an Amazonian rainforest blackwater catchment , 2006 .

[73]  O. Phillips,et al.  Impacts of global atmospheric change on tropical forests. , 2006, Trends in ecology & evolution.

[74]  O. Phillips,et al.  An international network to monitor the structure, composition and dynamics of Amazonian forests (RAINFOR) , 2002 .

[75]  W. Schlesinger,et al.  Forest carbon balance under elevated CO2 , 2002, Oecologia.

[76]  Jeffrey Q. Chambers,et al.  Tree damage, allometric relationships, and above-ground net primary production in central Amazon forest , 2001 .

[77]  J. V. Soares,et al.  Distribution of aboveground live biomass in the Amazon basin , 2007 .

[78]  L. Alves,et al.  Tree allometry and crown shape of four tree species in Atlantic rain forest, south-east Brazil , 2002, Journal of Tropical Ecology.

[79]  Y. Malhi,et al.  Spatial patterns and recent trends in the climate of tropical rainforest regions. , 2004, Philosophical transactions of the Royal Society of London. Series B, Biological sciences.

[80]  Kenneth L. Denman Canada Couplings between changes in the climate system and biogeochemistry , 2008 .

[81]  Martin Worbes,et al.  Annual growth rings, rainfall‐dependent growth and long‐term growth patterns of tropical trees from the Caparo Forest Reserve in Venezuela , 1999 .

[82]  D. Coomes,et al.  IMPACTS OF ROOT COMPETITION IN FORESTS AND WOODLANDS: A THEORETICAL FRAMEWORK AND REVIEW OF EXPERIMENTS , 2000 .

[83]  Yadvinder Malhi,et al.  Increasing dominance of large lianas in Amazonian forests , 2002, Nature.

[84]  J. Terborgh,et al.  Drought Sensitivity of the Amazon Rainforest , 2009, Science.

[85]  O. Phillips,et al.  After trees die: quantities and determinants of necromass across Amazonia , 2009 .

[86]  Michael Keller,et al.  Effects of Soil Texture on Belowground Carbon and Nutrient Storage in a Lowland Amazonian Forest Ecosystem , 2000, Ecosystems.

[87]  The RAINFOR database: monitoring forest biomass and dynamics , 2007 .

[88]  Yadvinder Malhi,et al.  Tropical forests and global atmospheric change: a synthesis. , 2004, Philosophical transactions of the Royal Society of London. Series B, Biological sciences.

[89]  J. Terborgh,et al.  The regional variation of aboveground live biomass in old‐growth Amazonian forests , 2006 .

[90]  L. Aragão,et al.  Factors controlling spatio‐temporal variation in carbon dioxide efflux from surface litter, roots, and soil organic matter at four rain forest sites in the eastern Amazon , 2007 .

[91]  J. Berry,et al.  Parameterization of Canopy Structure and Leaf-Level Gas Exchange for an Eastern Amazonian Tropical Rain Forest (Tapajós National Forest, Pará, Brazil) , 2005 .

[92]  S. Solomon The Physical Science Basis : Contribution of Working Group I to the Fourth Assessment Report of the Intergovernmental Panel on Climate Change , 2007 .

[93]  A. Di Fiore,et al.  Variation in wood density determines spatial patterns inAmazonian forest biomass , 2004 .

[94]  David A. Coomes,et al.  Mortality and tree‐size distributions in natural mixed‐age forests , 2007 .

[95]  S L Lewis,et al.  Pattern and process in Amazon tree turnover, 1976-2001. , 2004, Philosophical transactions of the Royal Society of London. Series B, Biological sciences.

[96]  J. Terborgh,et al.  The above‐ground coarse wood productivity of 104 Neotropical forest plots , 2004 .

[97]  W. Collins,et al.  Global climate projections , 2007 .

[98]  Frans Bongers,et al.  The ecology of lianas and their role in forests , 2002 .

[99]  S. Paton,et al.  ARE LIANAS INCREASING IN IMPORTANCE IN TROPICAL FORESTS? A 17‐YEAR RECORD FROM PANAMA , 2004 .

[100]  C. Tucker,et al.  Climate-Driven Increases in Global Terrestrial Net Primary Production from 1982 to 1999 , 2003, Science.

[101]  M. Buckeridge,et al.  Effect of atmospheric CO2 enrichment on the establishment of seedlings of Jatobá, Hymenaea Courbaril L. (Leguminosae, Caesalpinioideae) , 2002 .

[102]  O. Phillips,et al.  Infestation of trees by lianas in a tropical forest in Amazonian Peru , 2008 .

[103]  Bruce A. Wielicki,et al.  Evidence for Large Decadal Variability in the Tropical Mean Radiative Energy Budget , 2002, Science.

[104]  Jeffrey Q. Chambers,et al.  TROPICAL FORESTS : AN EVALUATION AND SYNTHESIS OF EXISTING FIELD DATA , 2022 .

[105]  J. Boone Kauffman,et al.  Ecosystem structure in the Brazilian Cerrado: a vegetation gradient of aboveground biomass, root mass and consumption by fire , 1998, Journal of Tropical Ecology.

[106]  S. Wofsy,et al.  The effects of biomass burning aerosols and clouds on the CO2 flux in Amazonia , 2007 .

[107]  J. Boone Kauffman,et al.  BIOMASS, CARBON, AND NUTRIENT DYNAMICS OF SECONDARY FORESTS IN A HUMID TROPICAL REGION OF MÉXICO , 1999 .

[108]  O. Phillips,et al.  Continental-scale patterns of canopy tree composition and function across Amazonia , 2006, Nature.

[109]  O. Campoe,et al.  Assessing the above-ground biomass of a complex tropical rainforest using a canopy crane , 2007 .

[110]  Robert J. Scholes,et al.  The Carbon Cycle and Atmospheric Carbon Dioxide , 2001 .

[111]  Yadvinder Malhi,et al.  Fingerprinting the impacts of global change on tropical forests. , 2004, Philosophical transactions of the Royal Society of London. Series B, Biological sciences.

[112]  G. Retallack A 300-million-year record of atmospheric carbon dioxide from fossil plant cuticles , 2001, Nature.

[113]  B. Forsberg,et al.  Biogeochemistry of carbon in the Amazon River , 1990 .

[114]  J. Chambers,et al.  Comprehensive assessment of carbon productivity, allocation and storage in three Amazonian forests , 2009 .

[115]  D. Sheil Evaluating turnover in tropical forests. , 1995, Science.

[116]  G. Kerstiens Meta-analysis of the interaction between shade-tolerance,light environment and growth response of woody species to elevated CO2 , 2001 .

[117]  F. Achard,et al.  Tropical forest cover change in the 1990s and options for future monitoring , 2005, Philosophical Transactions of the Royal Society B: Biological Sciences.

[118]  O. Phillips,et al.  Increasing Turnover Through Time in Tropical Forests , 1994, Science.