Representation of phosphorus cycle in Joint UK Land Environment Simulator (vn5.5_JULES-CNP)
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C. Quesada | S. Sitch | D. Clark | A. Wiltshire | L. Mercado | I. Hartley | M. Nakhavali | R. Assis | J. Camargo | S. Chadburn | K. Andersen | L. F. Lugli | Fernanda V. Cunha | Raffaello di Ponzio | G. Ribeiro | Lara Siebert | Anna C. M. Moraes | Jéssica Schmeisk Rosa | A. M. Moraes
[1] C. Quesada,et al. Fine roots stimulate nutrient release during early stages of leaf litter decomposition in a Central Amazon rainforest , 2021, Plant and Soil.
[2] Ying‐ping Wang,et al. Modelling of land nutrient cycles: recent progress and future development , 2021, Faculty reviews.
[3] S. Lewis,et al. Earth System Models Are Not Capturing Present‐Day Tropical Forest Carbon Dynamics , 2021, Earth's Future.
[4] P. Cox,et al. JULES-CN: a coupled terrestrial carbon–nitrogen scheme (JULES vn5.1) , 2021 .
[5] A. Rammig,et al. CO2 physiological effect can cause rainfall decrease as strong as large-scale deforestation in the Amazon , 2021 .
[6] Jinfeng Chang,et al. Global evaluation of the nutrient-enabled version of the land surface model ORCHIDEE-CNP v1.2 (r5986) , 2021 .
[7] S. Tiwari,et al. Direct foliar uptake of phosphorus from desert dust. , 2021, The New phytologist.
[8] L. Aragão,et al. Rapid responses of root traits and productivity to phosphorus and cation additions in a tropical lowland forest in Amazonia. , 2020, The New phytologist.
[9] Atul K. Jain,et al. Global Carbon Budget 2020 , 2020, Earth System Science Data.
[10] P. Cox,et al. Robust Ecosystem Demography (RED version 1.0): a parsimonious approach to modelling vegetation dynamics in Earth system models , 2020, Geoscientific Model Development.
[11] Victor O. Leshyk,et al. Integrating the evidence for a terrestrial carbon sink caused by increasing atmospheric CO2. , 2020, The New phytologist.
[12] P. Cox,et al. JULES-CN: a coupled terrestrial Carbon-Nitrogen Scheme (JULES vn5.1) , 2020 .
[13] J. Peñuelas,et al. Atmospheric deposition of elements and its relevance for nutrient budgets of tropical forests , 2020, Biogeochemistry.
[14] Jinfeng Chang,et al. Global evaluation of the nutrient enabled version of land surface model ORCHIDEE-CNP (v1.2) , 2020 .
[15] David Kenfack,et al. Asynchronous carbon sink saturation in African and Amazonian tropical forests , 2020, Nature.
[16] Yiqi Luo,et al. Global meta-analysis shows pervasive phosphorus limitation of aboveground plant production in natural terrestrial ecosystems , 2020, Nature Communications.
[17] Pierre Friedlingstein,et al. Carbon–concentration and carbon–climate feedbacks in CMIP6 models and their comparison to CMIP5 models , 2019, Biogeosciences.
[18] P. Cox,et al. The impact of a simple representation of non-structural carbohydrates on the simulated response of tropical forests to drought , 2019, Biogeosciences.
[19] Daniel M. Griffith,et al. Comment on “The global tree restoration potential” , 2019, Science.
[20] Anja Rammig,et al. Amazon forest response to CO2 fertilization dependent on plant phosphorus acquisition , 2019, Nature Geoscience.
[21] S. Zaehle,et al. The fate of carbon in a mature forest under carbon dioxide enrichment , 2019, bioRxiv.
[22] Yiqi Luo,et al. Quantifying Soil Phosphorus Dynamics: A Data Assimilation Approach , 2019, Journal of Geophysical Research: Biogeosciences.
[23] Silvia Caldararu,et al. Towards a more physiological representation of vegetation phosphorus processes in land surface models. , 2019, The New phytologist.
[24] L. Aragão,et al. Multiple phosphorus acquisition strategies adopted by fine roots in low-fertility soils in Central Amazonia , 2019, Plant and Soil.
[25] J. Hatfield,et al. Water-Use Efficiency: Advances and Challenges in a Changing Climate , 2019, Front. Plant Sci..
[26] J. Canadell,et al. Global trends in carbon sinks and their relationships with CO2 and temperature , 2018, Nature Climate Change.
[27] Benjamin Smith,et al. A new version of the CABLE land surface model (Subversion revision r4601) incorporating land use and land cover change, woody vegetation demography, and a novel optimisation-based approach to plant coordination of photosynthesis , 2018, Geoscientific Model Development.
[28] E. Mitchard. The tropical forest carbon cycle and climate change , 2018, Nature.
[29] P. Ciais,et al. A representation of the phosphorus cycle for ORCHIDEE (revision 4520) , 2017 .
[30] P. Reich,et al. Elevated CO2 does not increase eucalypt forest productivity on a low-phosphorus soil , 2017 .
[31] E. Burke,et al. A vertical representation of soil carbon in the JULES land surface scheme (vn4.3_permafrost) with a focus on permafrost regions , 2017 .
[32] O. Phillips,et al. Carbon uptake by mature Amazon forests has mitigated Amazon nations’ carbon emissions , 2017, Carbon Balance and Management.
[33] R. Siegwolf,et al. Growth and carbon relations of mature Picea abies trees under 5 years of free‐air CO2 enrichment , 2016 .
[34] Benjamin Smith,et al. Using models to guide field experiments: a priori predictions for the CO2 response of a nutrient‐ and water‐limited native Eucalypt woodland , 2016, Global change biology.
[35] P. Cox,et al. Improved representation of plant functional types and physiology in the Joint UK Land Environment Simulator (JULES v4.2) using plant trait information , 2016 .
[36] 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.
[37] Guangsheng Zhou,et al. Elevated-CO2 Response of Stomata and Its Dependence on Environmental Factors , 2016, Front. Plant Sci..
[38] E. Tipping,et al. The C:N:P:S stoichiometry of soil organic matter , 2016, Biogeochemistry.
[39] J. Gonçalves,et al. Labile and Non-Labile Fractions of Phosphorus and Its Transformations in Soil under Eucalyptus Plantations, Brazil , 2016 .
[40] S. Zaehle,et al. Does the growth response of woody plants to elevated CO2 increase with temperature? A model‐oriented meta‐analysis , 2015, Global change biology.
[41] S. Reed,et al. Incorporating phosphorus cycling into global modeling efforts: a worthwhile, tractable endeavor. , 2015, The New phytologist.
[42] Atul K. Jain,et al. Using ecosystem experiments to improve vegetation models , 2015 .
[43] W. Wanek,et al. The application of ecological stoichiometry to plant–microbial–soil organic matter transformations , 2015 .
[44] Yadvinder Malhi,et al. A comparison of plot‐based satellite and Earth system model estimates of tropical forest net primary production , 2015 .
[45] J. Terborgh,et al. Long-term decline of the Amazon carbon sink , 2015, Nature.
[46] C. Koven,et al. Multiple soil nutrient competition between plants, microbes, and mineral surfaces: model development, parameterization, and example applications in several tropical forests , 2015 .
[47] Benjamin L Turner,et al. Seasonal changes in soil organic matter after a decade of nutrient addition in a lowland tropical forest , 2015, Biogeochemistry.
[48] D. Schimel,et al. Effect of increasing CO2 on the terrestrial carbon cycle , 2014, Proceedings of the National Academy of Sciences.
[49] Mingzhu He,et al. Drought effect on plant nitrogen and phosphorus: a meta-analysis. , 2014, The New phytologist.
[50] K. Butterbach‐Bahl,et al. Short and long-term impacts of nitrogen deposition on carbon sequestration by forest ecosystems , 2014 .
[51] B. Nelson,et al. Improved allometric models to estimate the aboveground biomass of tropical trees , 2014, Global change biology.
[52] Duoying Ji,et al. Description and basic evaluation of Beijing Normal University Earth System Model (BNU-ESM) version 1 , 2014 .
[53] F. Woodward,et al. The relationship of leaf photosynthetic traits – Vcmax and Jmax – to leaf nitrogen, leaf phosphorus, and specific leaf area: a meta-analysis and modeling study , 2014, Ecology and evolution.
[54] P. Jones,et al. Updated high‐resolution grids of monthly climatic observations – the CRU TS3.10 Dataset , 2014 .
[55] J. Hartmann,et al. Global chemical weathering and associated p-release - the role of lithology, temperature and soil properties , 2014 .
[56] Mingguo Ma,et al. Carbon fluxes, evapotranspiration, and water use efficiency of terrestrial ecosystems in China , 2013 .
[57] M. G. Ryan. Three decades of research at Flakaliden advancing whole-tree physiology, forest ecosystem and global change research. , 2013, Tree physiology.
[58] K. Lindsay,et al. Twentieth-Century Oceanic Carbon Uptake and Storage in CESM1(BGC)* , 2013 .
[59] P. Cox,et al. Evaluating the Land and Ocean Components of the Global Carbon Cycle in the CMIP5 Earth System Models , 2013 .
[60] W. Post,et al. The role of phosphorus dynamics in tropical forests – a modeling study using CLM-CNP , 2013 .
[61] Benjamin L Turner,et al. Soil phosphorus responses to chronic nutrient fertilisation and seasonal drought in a humid lowland forest, Panama , 2013 .
[62] T. Crowther,et al. Carbon use efficiency and storage in terrestrial ecosystems. , 2013, The New phytologist.
[63] L. F. Lugli. Estoque de nutrientes na serrapilheira fina e grossa em função de fatores edáficos em florestas do Amazonas, Brasil , 2013 .
[64] A. Kirkevåg,et al. The Norwegian Earth System Model, NorESM1-M – Part 1: Description and basic evaluation of the physical climate , 2013 .
[65] Benjamin L Turner,et al. Pedogenesis, nutrient dynamics, and ecosystem development: the legacy of T.W. Walker and J.K. Syers , 2013, Plant and Soil.
[66] Y. Malhi,et al. Improving simulated Amazon forest biomass and productivity by including spatial variation in biophysical parameters , 2013 .
[67] Jens Hartmann,et al. The new global lithological map database GLiM: A representation of rock properties at the Earth surface , 2012 .
[68] Atul K. Jain,et al. The distribution of soil phosphorus for global biogeochemical modeling , 2012 .
[69] Corinna Hoose,et al. The Norwegian Earth System Model, NorESM1-M - Part 1: Description and basic evaluation , 2012 .
[70] J. Terborgh,et al. Basin-wide variations in Amazon forest structure and function are mediated by both soils and climate , 2012 .
[71] P. Ciais,et al. Fertile forests produce biomass more efficiently. , 2012, Ecology letters.
[72] M. Lieffering,et al. Effects of long-term exposure to enriched CO2 on the nutrient-supplying capacity of a grassland soil , 2012, Biology and Fertility of Soils.
[73] Jordi Sardans,et al. The C:N:P stoichiometry of organisms and ecosystems in a changing world: A review and perspectives , 2012 .
[74] Yadvinder Malhi,et al. The productivity, metabolism and carbon cycle of tropical forest vegetation , 2012 .
[75] Stephen Sitch,et al. Variations in Amazon forest productivity correlated with foliar nutrients and modelled rates of photosynthetic carbon supply , 2011, Philosophical Transactions of the Royal Society B: Biological Sciences.
[76] Y. Malhi,et al. The allocation of ecosystem net primary productivity in tropical forests , 2011, Philosophical Transactions of the Royal Society B: Biological Sciences.
[77] Xiaojuan Yang,et al. Phosphorus transformations as a function of pedogenesis: A synthesis of soil phosphorus data using Hedley fractionation method , 2011 .
[78] Sönke Zaehle,et al. Carbon–nitrogen interactions on land at global scales: current understanding in modelling climate biosphere feedbacks , 2011 .
[79] P. Cox,et al. The Joint UK Land Environment Simulator (JULES), model description – Part 2: Carbon fluxes and vegetation dynamics , 2011 .
[80] P. Cox,et al. The Joint UK Land Environment Simulator (JULES), model description – Part 1: Energy and water fluxes , 2011 .
[81] R. B. Jackson,et al. A Large and Persistent Carbon Sink in the World’s Forests , 2011, Science.
[82] Michael Kaspari,et al. Potassium, phosphorus, or nitrogen limit root allocation, tree growth, or litter production in a lowland tropical forest. , 2011, Ecology.
[83] Xin-ping Chen,et al. Phosphorus Dynamics: From Soil to Plant1 , 2011, Plant Physiology.
[84] Benjamin L Turner,et al. Phosphorus fractionation in lowland tropical rainforest soils in central Panama , 2010 .
[85] A. Arneth,et al. Variations in chemical and physical properties of Amazon forest soils in relation to their genesis , 2010 .
[86] Andrew D. Friend,et al. Carbon and nitrogen cycle dynamics in the O‐CN land surface model: 1. Model description, site‐scale evaluation, and sensitivity to parameter estimates , 2010 .
[87] E. Jimenez,et al. Fine root dynamics for forests on contrasting soils in the Colombian Amazon. , 2009 .
[88] O. Phillips,et al. Above- and below-ground net primary productivity across ten Amazonian forests on contrasting soils , 2009 .
[89] Yadvinder Malhi,et al. Basin-wide variations in foliar properties of Amazonian forest: phylogeny, soils and climate. , 2009 .
[90] Rachel M. Law,et al. A global model of carbon, nitrogen and phosphorus cycles for the terrestrial biosphere , 2009 .
[91] Stephen Sitch,et al. Modelling basin-wide variations in Amazon forest productivity – Part 1: Model calibration, evaluation and upscaling functions for canopy photosynthesis , 2009 .
[92] J. Chambers,et al. Comprehensive assessment of carbon productivity, allocation and storage in three Amazonian forests , 2009 .
[93] L. Anderson,et al. Soils of Amazonia with particular reference to the RAINFOR sites , 2009 .
[94] W. Knorr,et al. Quantifying photosynthetic capacity and its relationship to leaf nitrogen content for global‐scale terrestrial biosphere models , 2009 .
[95] N. Batjes,et al. The Harmonized World Soil Database , 2009 .
[96] I. C. Prentice,et al. Evaluation of the terrestrial carbon cycle, future plant geography and climate‐carbon cycle feedbacks using five Dynamic Global Vegetation Models (DGVMs) , 2008 .
[97] D. Jenkinson,et al. The turnover of organic carbon in subsoils. Part 2. Modelling carbon turnover , 2008 .
[98] William F. Laurance,et al. Dynamics of carbon, biomass, and structure in two Amazonian forests , 2008 .
[99] K. Treseder,et al. Nitrogen limitation of net primary productivity in terrestrial ecosystems is globally distributed. , 2008, Ecology.
[100] Helmut Hillebrand,et al. Global analysis of nitrogen and phosphorus limitation of primary producers in freshwater, marine and terrestrial ecosystems. , 2007, Ecology letters.
[101] Evan H. DeLucia,et al. Forest carbon use efficiency: is respiration a constant fraction of gross primary production? , 2007 .
[102] C. Field,et al. A model of biogeochemical cycles of carbon, nitrogen, and phosphorus including symbiotic nitrogen fixation and phosphatase production , 2007 .
[103] R. Schnur,et al. Climate-carbon cycle feedback analysis: Results from the C , 2006 .
[104] J. Terborgh,et al. The regional variation of aboveground live biomass in old‐growth Amazonian forests , 2006 .
[105] R. Siegwolf,et al. Carbon Flux and Growth in Mature Deciduous Forest Trees Exposed to Elevated CO2 , 2005, Science.
[106] N. Stephenson,et al. Forest turnover rates follow global and regional patterns of productivity. , 2005, Ecology letters.
[107] W. Parton,et al. Progressive Nitrogen Limitation of Ecosystem Responses to Rising Atmospheric Carbon Dioxide , 2004 .
[108] E. Davidson,et al. NITROGEN AND PHOSPHORUS LIMITATION OF BIOMASS GROWTH IN A TROPICAL SECONDARY FOREST , 2004 .
[109] G. Vourlitis,et al. Ecological research in the large-scale biosphere-atmosphere experiment in Amazonia: early results , 2004 .
[110] Peter M. Vitousek,et al. Nutrient Cycling and Limitation: Hawai'i as a Model System , 2004 .
[111] J. Terborgh,et al. The above‐ground coarse wood productivity of 104 Neotropical forest plots , 2004 .
[112] A. Di Fiore,et al. Variation in wood density determines spatial patterns inAmazonian forest biomass , 2004 .
[113] 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.
[114] Christopher B. Field,et al. Nitrogen and Climate Change , 2003, Science.
[115] E. Rastetter,et al. A model analysis of N and P limitation on carbon accumulation in Amazonian secondary forest after alternate land-use abandonment , 2003 .
[116] S. Hubbell,et al. Spatial and temporal variation of biomass in a tropical forest: results from a large census plot in Panama , 2003 .
[117] Pavel Kabat,et al. Comparative measurements of carbon dioxide fluxes from two nearby towers in a central Amazonian rainforest: the Manaus LBA site , 2002 .
[118] F. Chapin,et al. Principles of Terrestrial Ecosystem Ecology , 2002, Springer New York.
[119] Christopher B. Field,et al. FOREST CARBON SINKS IN THE NORTHERN HEMISPHERE , 2002 .
[120] L. Hedin,et al. Nitrogen loss from unpolluted South American forests mainly via dissolved organic compounds , 2002, Nature.
[121] Annika Nordin,et al. Soil nitrogen form and plant nitrogen uptake along a boreal forest productivity gradient , 2001, Oecologia.
[122] Sandy P. Harrison,et al. Global Biogeochemical Cycles in the Climate System , 2001 .
[123] Jason C. Neff,et al. Nutrient and mineralogical control on dissolved organic C, N and P fluxes and stoichiometry in Hawaiian soils , 2000 .
[124] H. Mooney,et al. Human Domination of Earth’s Ecosystems , 1997, Renewable Energy.
[125] R. McMurtrie,et al. Long-Term Response of Nutrient-Limited Forests to CO"2 Enrichment; Equilibrium Behavior of Plant-Soil Models. , 1993, Ecological applications : a publication of the Ecological Society of America.
[126] G. McCarty,et al. Effect of freeze-thaw events on mineralization of soil nitrogen , 1992, Biology and Fertility of Soils.
[127] G. Collatz,et al. Physiological and environmental regulation of stomatal conductance, photosynthesis and transpiration: a model that includes a laminar boundary layer , 1991 .
[128] L. Bruijnzeel. Nutrient input–output budgets of tropical forest ecosystems: a review , 1991, Journal of Tropical Ecology.
[129] J. Lynch,et al. The turnover of organic carbon and nitrogen in soil. , 1990 .
[130] J. Stewart,et al. Changes in Inorganic and Organic Soil Phosphorus Fractions Induced by Cultivation Practices and by Laboratory Incubations1 , 1982 .
[131] P. Sánchez,et al. Properties and Management of Soils in the Tropics , 1977 .
[132] Anja Rammig,et al. Model-data synthesis for the next generation of forest free-air CO2 enrichment (FACE) experiments. , 2016, The New phytologist.
[133] Stephen Porder,et al. Terrestrial phosphorus limitation: mechanisms, implications, and nitrogen-phosphorus interactions. , 2010, Ecological applications : a publication of the Ecological Society of America.
[134] S. Itch,et al. Evaluation of the terrestrial carbon cycle, future plant geography and climate-carbon cycle feedbacks using five Dynamic Global Vegetation Models (DGVMs) , 2008 .
[135] J. O H N,et al. Forest carbon use efficiency : is respiration a constant fraction of gross primary production ? , 2007 .
[136] Brasil.,et al. INSTITUTO NACIONAL DE PESQUISAS DA AMAZÔNIA –INPA , 2006 .
[137] J. Barlow,et al. IN AMAZONIAN FORESTS , 2004 .
[138] B. Kruijt,et al. Should phosphorus availability be constraining moist tropical forest responses to increasing CO2 concentrations , 2001 .
[139] F. S. Chapin,et al. The Mineral Nutrition of Wild Plants Revisited: A Re-evaluation of Processes and Patterns , 1999 .
[140] A. Varma,et al. Mycorrhiza , 1995, Springer Berlin Heidelberg.
[141] G. Collatz,et al. Coupled Photosynthesis-Stomatal Conductance Model for Leaves of C4 Plants , 1992 .
[142] Robert W. Howarth,et al. Nitrogen limitation on land and in the sea: How can it occur? , 1991 .
[143] J. Syers,et al. The fate of phosphorus during pedogenesis , 1976 .