The Effects of Phosphorus Cycle Dynamics on Carbon Sources and Sinks in the Amazon Region: A Modeling Study Using ELM v1

Tropical forests play a crucial role in the global carbon cycle, accounting for one third of the global net primary productivity and containing about 25% of global vegetation biomass and soil carbon. This is particularly true for tropical forests in the Amazon region, as these comprise approximately 50% of the world's tropical forests. It is therefore important for us to understand and represent the processes that determine the fluxes and storage of carbon in these forests. In this study, we show that the implementation of phosphorus (P) cycle and P limitation in the version 1 of the Energy Exascale Earth System Model land model (ELM v1) improves simulated spatial pattern of wood productivity. The P‐enabled ELM v1 is able to capture the declining west‐to‐east gradient of productivity, consistent with field observations. We also show that by improving the representation of mortality processes using soils data, ELMv1 is able to reproduce the observed spatial pattern of above ground biomass. Our model simulations show that the consideration of P availability leads to a smaller carbon sink associated with CO2 fertilization effect and lower carbon emissions due to land use and land cover change. Our simulations suggest P limitation would significantly reduce the carbon sink associated with CO2 fertilization effects through the 21st century. We conclude that P cycle dynamics affect both sources and sinks of carbon in the Amazon region, and the effects of P limitation would become increasingly important as CO2 increases. Therefore, P limitation must be considered for projecting future carbon dynamics in tropical ecosystems.

[1]  W. Wieder,et al.  Greater stem growth, woody allocation, and aboveground biomass in Paleotropical forests than in Neotropical forests. , 2019, Ecology.

[2]  E. Mitchard The tropical forest carbon cycle and climate change , 2018, Nature.

[3]  Benjamin L Turner,et al.  Plant responses to fertilization experiments in lowland, species-rich, tropical forests. , 2018, Ecology.

[4]  G. Hurtt Final Report: Enabling Land-Use in E3SM Land Model , 2018 .

[5]  Benjamin L Turner,et al.  Pervasive phosphorus limitation of tree species but not communities in tropical forests , 2018, Nature.

[6]  P. Thornton,et al.  The Impact of Parametric Uncertainties on Biogeochemistry in the E3SM Land Model , 2017 .

[7]  Dell,et al.  Contrasting carbon cycle responses of the tropical continents to the 2015–2016 El Niño , 2017, Science.

[8]  P. Ciais,et al.  Diagnosing phosphorus limitations in natural terrestrial ecosystems in carbon cycle models , 2017, Earth's future.

[9]  D. Metcalfe,et al.  Informing climate models with rapid chamber measurements of forest carbon uptake , 2017, Global change biology.

[10]  O. Phillips,et al.  Carbon uptake by mature Amazon forests has mitigated Amazon nations’ carbon emissions , 2017, Carbon Balance and Management.

[11]  F. Hoffman,et al.  Phosphorus feedbacks constraining tropical ecosystem responses to changes in atmospheric CO2 and climate , 2016 .

[12]  Ke Zhang,et al.  Variation in stem mortality rates determines patterns of above‐ground biomass in Amazonian forests: implications for dynamic global vegetation models , 2016, Global change biology.

[13]  Arief Wijaya,et al.  An integrated pan‐tropical biomass map using multiple reference datasets , 2016, Global change biology.

[14]  Steven W. Running,et al.  Large divergence of satellite and Earth system model estimates of global terrestrial CO2 fertilization , 2016 .

[15]  M. Coe,et al.  Changing Amazon biomass and the role of atmospheric CO2 concentration, climate, and land use , 2016 .

[16]  Anja Rammig,et al.  Model-data synthesis for the next generation of forest free-air CO2 enrichment (FACE) experiments. , 2016, The New phytologist.

[17]  S. Reed,et al.  Incorporating phosphorus cycling into global modeling efforts: a worthwhile, tractable endeavor. , 2015, The New phytologist.

[18]  William R. Wieder,et al.  Future productivity and carbon storage limited by terrestrial nutrient availability , 2015 .

[19]  J. Terborgh,et al.  Long-term decline of the Amazon carbon sink , 2015, Nature.

[20]  L. Hedin Biogeochemistry: Signs of saturation in the tropical carbon sink , 2015, Nature.

[21]  Ke Zhang,et al.  The fate of Amazonian ecosystems over the coming century arising from changes in climate, atmospheric CO2, and land use , 2015, Global change biology.

[22]  J. Terborgh,et al.  Markedly divergent estimates of Amazon forest carbon density from ground plots and satellites , 2014, Global ecology and biogeography : a journal of macroecology.

[23]  Michael Obersteiner,et al.  Human-induced nitrogen–phosphorus imbalances alter natural and managed ecosystems across the globe , 2013, Nature Communications.

[24]  S. Higgins,et al.  On the potential vegetation feedbacks that enhance phosphorus availability – insights from a process-based model linking geological and ecological timescales , 2013 .

[25]  M. Torn,et al.  The effect of vertically resolved soil biogeochemistry and alternate soil C and N models on C dynamics of CLM4 , 2013 .

[26]  W. Post,et al.  The role of phosphorus dynamics in tropical forests – a modeling study using CLM-CNP , 2013 .

[27]  Mollie E. Brooks,et al.  A direct test of nitrogen and phosphorus limitation to net primary productivity in a lowland tropical wet forest. , 2013, Ecology.

[28]  D. Clark,et al.  Field‐quantified responses of tropical rainforest aboveground productivity to increasing CO2 and climatic stress, 1997–2009 , 2013 .

[29]  Y. Malhi,et al.  Improving simulated Amazon forest biomass and productivity by including spatial variation in biophysical parameters , 2013 .

[30]  Stephen Sitch,et al.  Simulated resilience of tropical rainforests to CO2-induced climate change , 2013 .

[31]  Bettina M. J. Engelbrecht,et al.  Species distributions in response to individual soil nutrients and seasonal drought across a community of tropical trees , 2013, Proceedings of the National Academy of Sciences.

[32]  P. Cox,et al.  Sensitivity of tropical carbon to climate change constrained by carbon dioxide variability , 2013, Nature.

[33]  O. Phillips,et al.  Residence times of woody biomass in tropical forests , 2013 .

[34]  Zong-Liang Yang,et al.  Technical description of version 4.5 of the Community Land Model (CLM) , 2013 .

[35]  S. Reed,et al.  Tropical forest carbon balance in a warmer world: a critical review spanning microbial‐ to ecosystem‐scale processes , 2012, Biological reviews of the Cambridge Philosophical Society.

[36]  Daniel S. Goll,et al.  Nutrient limitation reduces land carbon uptake in simulations with a model of combined carbon, nitrogen and phosphorus cycling , 2012 .

[37]  J. Terborgh,et al.  Basin-wide variations in Amazon forest structure and function are mediated by both soils and climate , 2012 .

[38]  S. Goetz,et al.  Estimated carbon dioxide emissions from tropical deforestation improved by carbon-density maps , 2012 .

[39]  Yadvinder Malhi,et al.  The productivity, metabolism and carbon cycle of tropical forest vegetation , 2012 .

[40]  Xiaojuan Yang,et al.  Phosphorus transformations as a function of pedogenesis: A synthesis of soil phosphorus data using Hedley fractionation method , 2011 .

[41]  Stephen Porder,et al.  Relationships among net primary productivity, nutrients and climate in tropical rain forest: a pan-tropical analysis. , 2011, Ecology letters.

[42]  R. B. Jackson,et al.  A Large and Persistent Carbon Sink in the World’s Forests , 2011, Science.

[43]  Michael Kaspari,et al.  Potassium, phosphorus, or nitrogen limit root allocation, tree growth, or litter production in a lowland tropical forest. , 2011, Ecology.

[44]  P. Ciais,et al.  Mortality as a key driver of the spatial distribution of aboveground biomass in Amazonian forest: results from a dynamic vegetation model , 2010 .

[45]  Wolfgang Lucht,et al.  Estimating the risk of Amazonian forest dieback. , 2010, The New phytologist.

[46]  Stephen Sitch,et al.  Multiple mechanisms of Amazonian forest biomass losses in three dynamic global vegetation models under climate change. , 2010, The New phytologist.

[47]  A. Arneth,et al.  Variations in chemical and physical properties of Amazon forest soils in relation to their genesis , 2010 .

[48]  Stephen Porder,et al.  Terrestrial phosphorus limitation: mechanisms, implications, and nitrogen-phosphorus interactions. , 2010, Ecological applications : a publication of the Ecological Society of America.

[49]  O. Phillips,et al.  Above- and below-ground net primary productivity across ten Amazonian forests on contrasting soils , 2009 .

[50]  Rachel M. Law,et al.  A global model of carbon, nitrogen and phosphorus cycles for the terrestrial biosphere , 2009 .

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

[52]  A. Arneth,et al.  Chemical and physical properties of Amazon forest soils in relation to their genesis , 2009 .

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

[54]  Naota Hanasaki,et al.  GSWP-2 Multimodel Analysis and Implications for Our Perception of the Land Surface , 2006 .

[55]  H. L. Allen,et al.  Bioavailability of slowly cycling soil phosphorus: major restructuring of soil P fractions over four decades in an aggrading forest , 2006, Oecologia.

[56]  N. Mahowald,et al.  Atmospheric global dust cycle and iron inputs to the ocean , 2005 .

[57]  Peter E. Thornton,et al.  Assessing future nitrogen deposition and carbon cycle feedback using a multimodel approach: Analysis of nitrogen deposition , 2005 .

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

[59]  R. Houghton,et al.  Annual fluxes of carbon from deforestation and regrowth in the Brazilian Amazon , 2000, Nature.

[60]  H. Tian,et al.  Effect of interannual climate variability on carbon storage in Amazonian ecosystems , 1998, Nature.

[61]  J. Syers,et al.  The fate of phosphorus during pedogenesis , 1976 .