Terrestrial vegetation removes CO2 from the atmosphere; an important climate regulation service that slows global warming. This 119 Pg C per annum transfer of CO2 into plants—gross primary productivity (GPP)—is the largest land carbon flux globally. While understanding past and anticipated future GPP changes is necessary to support carbon management, the factors driving long-term changes in GPP are largely unknown. Here we show that 1901 to 2010 changes in GPP have been dominated by anthropogenic activity. Our dual constraint attribution approach provides three insights into the spatiotemporal patterns of GPP change. First, anthropogenic controls on GPP change have increased from 57% (1901 decade) to 94% (2001 decade) of the vegetated land surface. Second, CO2 fertilization and nitro gen deposition are the most important drivers of change, 19.8 and 11.1 Pg C per annum (2001 decade) respectively, especially in the tropics and industrialized areas since the 1970’s. Third, changes in climate have functioned as fertilization to enhance GPP (1.4 Pg C per annum in the 2001 decade). These findings suggest that, from a land carbon balance perspective, the Anthropocene began over 100 years ago and that global change drivers have allowed GPP uptake to keep pace with anthropogenic emissions.
Our understanding of changes in Earth system processes depends on models1,2. Model-based attribution, quantifying the importance and magnitude of causal factors for a detected change3, is routinely used to assess the relative contributions of anthropogenic factors and natural variability on Earth system phenomena, ranging from precipitation extremes to decadal-scale changes in net carbon uptake4,5,6,7,8. For land carbon metabolism, attribution typically focuses on net land uptake of CO2 (ref. 9). While this quantity is important to inform climate policy, e.g., Paris Climate Accords, it is the disequilibrium across many processes—such as heterotrophic respiration and fire emissions—with uncertain magnitude and spatiotemporal patterns7,9,10. This suggests that an improved understanding of the net land-atmosphere CO2 signal can be achieved by examining each component flux, and relevant drivers of change, individually.
Here we use a novel dual constraint approach to attribute centennial scale changes in GPP at grid cell to global scales. GPP is of central importance for the net carbon balance as it represents the entry of carbon into land ecosystems such that all other processes are downstream. We quantify changes in GPP due to natural climate variability, land use/land cover change, greenhouse gases, and nitrogen deposition. Our approach uses two broad ensembles of Earth system models (ESMs): (1) a 11-member ensemble of observation-driven land surface models—corresponding to the land component of ESMs in offline mode—from the Multi-scale synthesis and Terrestrial Model Intercomparison Project (MsTMIP) (ref. 11); and (2) an 13-member ensemble of fully coupled ESMs from CMIP5, the fifth phase of the Coupled Model Intercomparison Project12. We also use machine learning to recover the change in GPP for the individual offline climatic factors of heat (near-surface air temperature), water (precipitation), and light (downwelling shortwave radiation). This is based on the emulation (see Methods) of MsTMIP where only climate varies and then sequentially retrieving the contribution of each climatic factor by simulation differencing9.
Enhanced GPP is the basis by which land ecosystems buffer climate change. Model-based reconstructions indicate significant changes in gross uptake of carbon by the vegetated land surface over the 20th Century. From 1901 to 2010 GPP has increased globally (Fig. 1) by 10.5 Pg C per annum (uncertainty range: +8.2 to +12.4 Pg C per annum), in qualitative agreement with long-term atmospheric records of carbonyl sulfide13, and equivalent to 9% of current satellite-era global GPP of 119 Pg C per annum2. Increases in GPP are centered on the tropics as well as forested regions of the USA and Eurasia. In addition, both amplitude (difference between seasonal maximum and minimum) and volatility (changes in year-to-year variation) have increased. Changes in amplitude are most pronounced in the Northern Hemisphere (Fig. 1) and are overwhelmingly positive; by area 60% of vegetated land ecosystems have seen an increase versus only 2% where a decline occurred. The spatial footprint of changes in volatility shows that 62% of vegetated land ecosystems have seen at least a doubling of volatility versus <1% where volatility decreased. The largest changes in volatility, where year-to-year changes are at least tenfold larger in the satellite-era, are centered on the northern high latitudes and the Eurasian Steppe (Fig. 1), supporting the importance of these regions—particularly arid and dryland systems–in driving the interannual variability and trend of net carbon uptake14.
We find that anthropogenic forcings—primarily well-mixed greenhouse gases (see Methods)—are the source of these changes in GPP. Indeed, from the perspective of GPP we had already entered the Anthropocene, where human agency represents the most important geological forcing15, no later than the turn of the 20th Century. Integrated globally, the impactof anthropogenic forcings has increased from -0.1 (1901 decade) to +15.6 Pg C per annum (2001 decade) and acts to enhance GPP. In contrast, natural forcings (solar irradiance and volcanic aerosols) show an ever changing, over space and time, pattern of small effect sizes (typically <1 Pg C per annum globally in absolute value with a mean of -0.02 Pg C per annum from 1901 to 2010; Extended Data Fig. 1) with the largest volatility in the tropics. Spatial footprints in the first decade of both the 20th and 21st Centuries show a predominance of anthropogenic factors (Fig. 2) with changes in GPP across 57% (1901 decade) and 94% (2001 decade) of all vegetated land ecosystems linked to human agency. Through time there is a clear trend toward total anthropogenic control of changes in GPP.
Among individual attribution factors considered, changes associated with the CO2 fertilization effect and nitrogen deposition are largest (Fig. 3). The CO2 effect has monotonically increased from +3.7 (1901 decade) to +19.8 Pg C per annum (2001 decade); a fivefold increase now equivalent to 17% of contemporary global GPP2. The impact of CO2 fertilization is most pronounced in the tropics and Southeast Asia (Fig. 3) and shows an increasing trend and spatial footprint poleward from the equator since the 1960’s (Extended Data Fig. 2). Nitrogen deposition (Fig. 3) has similarly acted to enhance GPP. This effect has grown from +1.6 (1901 decade) to +11.1 Pg C per annum (2001 decade) and is focused on industrialized areas in North America, Europe, and China (Extended Data Fig. 2). In contrast, land use and land cover change (LULCC) is associated with a negative impact globally (-1.3 Pg C per annum across all decades or 1% of contemporary global GPP) and the most relative uncertainty (Fig. 3). These impacts —driven by degrading high GPP systems (forests) to low GPP systems (shrublands)—are dominant in the eastern USA, Europe, China, and the tropics. Unlike CO2 and nitrogen deposition, the LULCC effect is less variable in time; it shows a relatively static spatial footprint through the 20th Century (Extended Data Fig. 2).
Using a machine learning-based approach to decompose the net climate signal from the MsTMIP ensemble into temperature, precipitation, and radiation effects (see Methods) we find that climate change has functioned as climate fertilization—changes in climate have acted to increase gross uptake. Globally this effect is modest (Fig. 4), with a long-term average of +0.3 Pg C per annum, but has increased in recent decades to +1.4 Pg C per annum (2001 decade), equivalent to 50% of the contemporary net land sink1. Of all three climate effects temperature elicits the largest changes in GPP (Fig. 4) and has the largest spatial footprint (Fig. 5) while changes in radiation exhibit only a weak influence on GPP. Spatially, and in agreement with the effect of growing season temperature on peak GPP16, we find that temperature has enhanced GPP in the mid to northern latitudes. In contrast, 20th Century changes in temperature and precipitation have acted to depress GPP in the tropics (Fig. 4). Even though changes in climate are important regionally and exhibit a similar overall areal extent as LULCC, the spatial footprint of changes in GPP is driven by CO2 fertilization. Across 58% of the vegetated land surface changes in CO2 serve as the most dominant factor (Fig. 5).
While ESMs agree that anthropogenic factors have dominated changes in GPP over the 20th Century, care is warranted in interpretation. What constitutes an anthropogenic forcing varies across the CMIP5 ensemble and not all MsMTIP models simulate each sequential control. This is reflected in the confidence bounds (see Methods) for each factor. The total change due to CMIP5 anthropogenic forcings in the 2001 decade is +15.6 Pg C per annum, albeit with substantial uncertainty (+10.4 to +43.5 Pg C per annum). This is lower than but consistent with the corresponding figure from MsTMIP—equating the effects of CO2 fertilization, nitrogen deposition, and LULCC to anthropogenic forcings—of +25.6 Pg C per annum (uncertainty range: +16.1 to +35.8 Pg C per annum). This, in turn, matches the sum, +29.3 Pg C per annum (uncertainty range: +19.6 to +39.7 Pg C per annum), of individual anthropogenic factors (CO2 fertilization, nitrogen deposition, and LULCC) explicitly considered across both CMIP5 and MsTMIP ensembles. This consistency is supported by the similar effect sizes of CO2 fertilization and LULCC individually (nitrogen subsidy is only addressed in MsTMIP) across both ensembles (Extended Data Fig. 3). Finally, adjusting the CO2 effect downward to correct for the missing (and negative) vegetation-carbon feedback component of CO2 fertilization17 lowers this human agency effect to +24.8 Pg C per annum, again consistent with both CMIP5 and MsTMIP ensembles. In any case, the dominance of anthropogenic drivers in controlling changes in GPP since 1901 is clear, with CO2 fertilization and nitrogen subsidy the most important drivers in time, space (for CO2 only), and magnitude.
Despite this secular trend in GPP, there is substantial unresolved ambiguity surrounding both leading anthropogenic drivers in CMIP5 and MsTMIP. Evidence supporting the CO2 fertilization effect—the dominant driver of GPP enhancement since 1901—is supported by first principles of plant physiology but is otherwise mixed. According to recent studies, the CO2 fertilization effect is simultaneously underestimated for GPP in ESMs18, overestimated for NPP (GPP after autotrophic respiration has been subtracted) relative to satellite-derived products19, or not present in biomass growth for undisturbed tropical forests20 or in tree growth for western Canadian subalpine forests21. In contrast, a 100 ppm increase (roughly the 20th Century) in CO2 is linked to a 35% increase in net photosynthesis based on isotopic signatures of deuterium in historic plant material and manipulation experiments22. Furthermore, when warming and CO2 fertilization are considered jointly, the latter is not associated with any growth enhancement, as seen in the Canadian boreal forest23 and in high-elevation forests of central Mexico24. Moreover, there are clear indications of sink saturation, suggesting on upper limit of uptake, especially in forest systems25. Finally, neither CMIP5 nor MsTMIP allow the vegetation-carbon feedback component of increasing CO2 concentrations to be quantified, potentially resulting in a 30% overestimation of the CO2 fertilization effect17.
A similar ambiguity concerns the effects of nitrogen subsidy. These occur in the context of a critical load past which additional nitrogen inputs have potentially deleterious impacts on ecosystem function, from mortality to changes in community composition, carbon allocation and growth rates26,27. For extratropical forests this critical load is estimated at 10 to 20 kg N/ha per annum overall26 but can be significantly lower for specific forest types, e.g., USA northern forests show declined survivorship at as low as 3 kg N/ha per annum27. In tropical forests the knowledge base is more limited and experimental evidence for a significant positive effect equivocal28,29. This holds especially in primary and lowland forests and is linked to phosphorous availability28,30, which is not addressed in either ensemble. Focusing on MsTMIP, where nitrogen subsidy increases by a factor of five, the percent area of impacted extratropical forests where positive nitrogen subsidy exceeds the minimum threshold increases monotonically from 1% (1901 decade) to 29% (2001 decade). External nitrogen inputs also always enhance gross uptake in tropical forests (Fig. 3), with a mean subsidy of 3.5 kg N/ha per annum—increasing monotonically from 1.1 (1901 decade) to 8.6 kg N/ha per annum (2001 decade)—eliciting a mean GPP increase of 30.1 g C/m2 per annum.
Both CMIP5 and MsTMIP heavily condition on the CO2 fertilization effect and—especially for MsTMIP models with carbon-nitrogen coupling9—external nitrogen to drive positive changes in gross carbon uptake. This occurs without any sign of agnostic effects or saturation; both nitrogen subsidy and levels of CO2 are highly correlated (ρ = 0.99) with GPP across decades globally. This is problematic in that resolving the efficacy of both anthropogenic drivers is a prerequisite to reducing the persistent and large uncertainties in the carbon cycle-climate feedback10,31. Beyond this, there are other innovations needed to narrow the range in simulated values. Especially relevant for changes in GPP is the treatment of agricultural systems where there is strong evidence that modeled estimates of GPP are systematically biased low32. As CMIP5 and MsTMIP do not include explicit crop modeling, attributed changes in GPP, particularly in the context of LULCC, are likely skewed. Evidence that recent enhanced global GPP is driven by croplands33 reinforces the nascent trend of embedding agriculture submodules into coupled Earth system models32,34.
More generally, state-of-the-art land modeling frameworks still lack processes that materially impact trajectories of GPP; such as nutrient cycling, dynamic vegetation and disturbance35,36. The increasing complexity of modeling frameworks and questions asked of them itself requires an updated approach to address heterogeneity in process representation, tiling schemes that vary by process within model, and tracking changes in parametrizable ecosystem properties36. Focusing on the lead anthropogenic drivers over the 20th Century, knowledge base improvements for the CO2 fertilization effect and explicit parameterizable linkages between carbon cycling to nitrogen and phosphorus biogeochemistry37 are crucial to better constrain global GPP. This, in turn, points to the need of continuous iteration between modeling, data science, and experimental communities to improve predictive capacity36. As there is already evidence that future estimates of net carbon cycling may be biased upward when nutrient limitation is not considered9,38, a more robust treatment is more urgent still given the diminishing climate policy window to effect meaningful change in the trajectory of global change, past drivers of GPP enhancement notwithstanding.
We use historical reconstructions of gross primary productivity (GPP) from offline and fully coupled state-of-the-art Earth system models (ESMs). Offline reconstructions are drawn from 11 terrestrial biosphere simulators in the Multi-scale synthesis and Terrestrial Model Intercomparison Project (MsTMIP Version 1; https://doi.org/10.3334/ORNLDAAC/1225) (ref. 11,39). MsTMIP uses a constrained simulation protocol (driving data, vegetation cover, boundary conditions, and steady-state spin-up protocol are all standardized; only model structure varies). All runs use observation-based driving d ata to replicate 1901 to 2010 historical conditions34 with a semi-factorial design where time-varying factors of climate (SG1), land cover and land use change (LULCC) (SG2), [CO2] (SG3), and nitrogen deposition (BG1) are sequentially enabled after steady-state (RG1)—the reference run11,39 based on a repeated cycle of a randomized 30-yr block of trend-free weather—is achieved (MsTMIP simulation name in parenthesis). MsTMIP models used for this study are CLM, CLM4VIC, DLEM, GTEC, ISAM, LPJ-wsl, ORCHIDEE-LSCE, SiBCASA, TEM6, VEGAS2.1 and VISIT. Only CLM, CLM4VIC, DLEM and TEM6 simulate BG1, i.e., have carbon-nitrogen coupling.
Fully coupled reconstructions for 1901 to 2010 for 13 ESMs (Extended Data Table 1) are taken from the CMIP5 archive (http://cmip-pcmdi.llnl.gov/cmip5/data_portal.html). CMIP5, the fifth phase of the Coupled Model Intercomparison Project, serves as a central repository for ESM simulations that inform the Fifth Assessment Report (AR5) of the Intergovernmental Panel on Climate Change (IPCC) (https://ipcc.ch/report/ar5/). CMIP5 is designed to provide a multi-model framework to investigate model differences in carbon cycle and cloud-based feedbacks as well as climate predictability and the range in ESM responses from similar forcing inputs12. For this study ESMs are chosen based on simulation experiment availability. Each ESM has, at a minimum, a preindustrial control (piControl) and historical (historical) experiments (CMIP5 simulation experiment name in parenthesis; see Extended Data Table 1). In addition, experiments that differ from piControl or historical by a single factor (or factor set, e.g., all anthropogenic forcings) are also included: (1) with greenhouse gas forcing only (historicalGHG), (2) with natural forcing only (historicalNat), (3) with LULCC only and/or (4) with anthropogenic forcings only (variants of historicalMisc). Finally, two fully coupled carbon/climate experiments are included if available: (1) the carbon cycle sees preindustrial levels of CO2 but the radiation code sees historical conditions (esmFdbk2) and (2) the radiation code sees preindustrial levels of CO2 but the carbon cycle sees historical CO2 (esmFixClim2). In all cases only one realization per ESM is used; land carbon cycling is driven by model structure and therefore insensitive to initial conditions.
For both offline and coupled reconstructions we analyze annual values as global aggregates as well as by grid cell. For mapped values CMIP5 reconstructions are resampled to a half-degree spatial resolution to match the MsTMIP land mask and use the barren mask from a contemporary upscaled eddy covariance product2. Our results are based on integration over the full ensemble of ESMs—the consensus ensemble mean40—using “one-model-one-vote” (ref. 41) and assume that an unweighted multi-model mean is the best estimate42,43,44. We note that not all reconstructions share the same set of simulation experiments. Uncertainty is calculated as ensemble spread based on bootstrapping with 1000 bootstrap replicates and is expressed as 90% confidence intervals throughout.
Attribution is based on differencing9. For CMIP5 and MsTMIP, we assume the difference between two simulations is solely attributable to the relevant factor, e.g., subtracting SG2 from SG3 recovers the effect of time-varying [CO2] as both MsTMIP simulations are identical apart from SG3 having dynamic [CO2] enabled. Similarly, in CMIP5, subtracting piControl from historicalNat GPP recovers the effect of natural forcings only as both simulations are identical apart from historicalNat including changes in natural forcings–solar irradiance and volcanic aerosols.
For climatic factors (near-surface air temperature, precipitation, and downwelling shortwave radiation) the effect of each is recovered using a machine learning-based emulator of MsTMIP run SG1 (time-varying climate only). Here the random forest algorithm45 is trained with SG1 GPP as the target and near-surface air temperature, precipitation, and downwelling shortwave radiation as explanatory variables. The explanatory variables are those used in forcing all offline MsTMIP runs and are identical across all MsTMIP models. Training is done by grid cell at monthly time step for each MsTMIP model individually. For the SG1 emulation (Extended Data Fig. 4) median variance explained, in a least-squares sense based on those observations not used in training (out-of-bag data points), is at least 93% across all models and all grid cells. As the climate space used to force RG1 is a randomized subset of that used to force SG1 (ref. 33,34) the random forest algorithm does not have to extrapolate beyond the limits of the training data. As such the emulation of RG1 shows equivalent skill (Extended Data Fig. 4) with median variance explained of 96%. For both emulations, skill across space is highly similar with the lowest skill in the Indonesian tropics and Australia and the highest skill across the extratropical Northern Hemisphere.
The effect of each climatic factor is then calculated by differencing after sequentially enabling downwelling shortwave radiation, precipitation, and then near-surface air temperature in the emulator. As an illustration, the effect of downwelling shortwave radiation is recovered based on the difference between two emulations: the RG1 case (all climate explanatory variables use RG1 climate) subtracted from the emulation where SG1 downwelling shortwave radiation is paired with RG1 precipitation and RG1 near-surface air temperature. While the emulator offers a computationally inexpensive approach to attribute changes in GPP to individual climate drivers it is not process-aware but rather maps changes in climate to instantaneous changes in GPP. As such, the emulator provides only a first-order assessment (interaction terms are excluded) of how each climate driver impacts GPP without having to formally execute additional MsTMIP simulations. It is important to note that climatic effects cannot be precisely attributed to anthropogenic or natural forcings. In MsTMIP prescribed forcing data is based on historical information, i.e., contains a mix of anthropogenic changes as well as natural variability in Earth’s climate system.
In total we attribute changes in GPP from 1901 to 2010 to seven single factors and two factor sets: climate, LULCC, [CO2], nitrogen deposition, near-surface air temperature, precipitation, and downwelling shortwave radiation as well as all natural forcings (changes in solar irradiance and volcanic aerosols) vs. all anthropogenic forcings (with emphasis on well-mixed greenhouse gases and LULCC; see Extended Data Table 1). We note that attributed changes at 1901, the start of the analysis period, are not a priori zero as anthropogenic impacts on carbon cycling predate 1901.
MsTMIP Version 1 data are available without restriction through the Oak Ridge National Laboratory’s Distributed Active Archive Center (ORNL DAAC; https://daac.ornl.gov/) at https://doi.org/10.3334/ORNLDAAC/1225. CMIP5 data are available without restriction through the Earth System Grid Federation (ESGF) as hosted at the Lawrence Livermore National Laboratory at https://esgf-node.llnl.gov/projects/esgf-llnl/.
Le Quéré, C. et al. Global Carbon Budget 2017, Earth Syst. Sci. Data 10, 405–448, https://doi.org/10.5194/essd-10-405-2018 (2018).
Jung, M. et al. Compensatory water effects link yearly global land CO2 sink changes to temperature. Nature 541(7638), 516–520 (2017).
Hegerl, G.C. et al. Good Practice Guidance Paper on Detection and Attribution Related to Anthropogenic Climate Change. In: Meeting Report of the Intergovernmental Panel on Climate Change Expert Meeting on Detection and Attribution of Anthropogenic Climate Change [Stocker, T.F., C.B. Field, D. Qin, V. Barros, G.-K. Plattner, M. Tignor, P.M. Midgley, and K.L. Ebi (eds.)]. IPCC Working Group I Technical Support Unit, University of Bern, Bern, Switzerland, (2010).
Bellassen, V. et al. Reconstruction and attribution of the carbon sink of European forests between 1950 and 2000. Global Change Biology 17(11), 3274–3292 (2011).
Fernández-Martínez, M. et al. Global trends in carbon sinks and their relationships with CO 2 and temperature. Nature Climate Change 9, 73–79 (2018).
Ribes, A., Zwiers, F. W., Azaïs, J. M. & Naveau, P. A new statistical approach to climate change detection and attribution. Climate Dynamics 48(1–2), 367–386 (2017).
Tian, H. et al. China’s terrestrial carbon balance: Contributions from multiple global change factors. Global Biogeochem. Cycles 25, GB1007, https://doi.org/10.1029/2010GB003838 (2011).
Williams, C. A. et al. Interannual variability of photosynthesis across Africa and its attribution. J. Geophys. Res. 113, G04015, https://doi.org/10.1029/2008JG000718 (2008).
Huntzinger, D. N. et al. Uncertainty in the response of terrestrial carbon sink to environmental drivers undermines carbon-climate feedback predictions. Scientific Reports 7(1), 4765 (2017).
Friedlingstein, P. et al. Uncertainties in CMIP5 climate projections due to carbon cycle feedbacks. Journal of Climate 27(2), 511–526 (2014).
Huntzinger, D. N. et al. The North American Carbon Program Multi-scale synthesis and Terrestrial Model Intercomparison Project – Part 1: Overview and experimental design, Geosci. Model Dev. 6, 2121–2133, https://doi.org/10.5194/gmd-6-2121-2013 (2013).
Taylor, K. E., Stouffer, R. J. & Meehl, G. A. An overview of CMIP5 and the experiment design. Bulletin of the American Meteorological Society 93(4), 485–498 (2012).
Campbell, J. E. et al. Large historical growth in global terrestrial gross primary production. Nature 544(7648), 84–87 (2017).
Ahlström, A. et al. The dominant role of semi-arid ecosystems in the trend and variability of the land CO2 sink. Science 348(6237), 895–899 (2015).
Crutzen, P. J. Geology of mankind. Nature 415(6867), 23–23 (2002).
Zhou, S., et al. (2017). Dominant role of plant physiology in trend and variability of gross primary productivity in North America. Scientific Reports, 7 (2017).
Zhu, P. et al. Elevated atmospheric CO2 negatively impacts photosynthesis through radiative forcing and physiology-mediated climate feedback. Geophysical Research Letters 44(4), 1956–1963 (2017).
Sun, Y. et al. Impact of mesophyll diffusion on estimated global land CO2 fertilization. Proceedings of the National Academy of Sciences 111(44), 15774–15779 (2014).
Smith, W. K. et al. Large divergence of satellite and Earth system model estimates of global terrestrial CO2 fertilization. Nature Climate Change 6(3), 306 (2016).
van der Sleen, P. et al. No growth stimulation of tropical trees by 150 years of CO2 fertilization but water-use efficiency increased. Nature Geoscience 8(1), 24 (2015).
Hararuk, O., Campbell, E. M., Antos, J. A., & Parish, R. Tree rings provide no evidence of a CO2 fertilization effect in old-growth subalpine forests of western Canada. Global change biology, https://doi.org/10.1111/gcb.14561 (2018).
Ehlers, I. et al. Detecting long-term metabolic shifts using isotopomers: CO2-driven suppression of photorespiration in C3 plants over the 20th century. Proceedings of the National Academy of Sciences 112(51), 15585–15590 (2015).
Girardin, M. P. et al. No growth stimulation of Canada’s boreal forest under half-century of combined warming and CO2 fertilization. Proceedings of the National Academy of Sciences 113(52), E8406–E8414 (2016).
Gómez-Guerrero, A. et al. Growth decline and divergent tree ring isotopic composition (δ13C and δ18O) contradict predictions of CO2 stimulation in high altitudinal forests. Global Change Biology 19(6), 1748–1758 (2013).
Zhu, K., Zhang, J., Niu, S., Chu, C. & Luo, Y. Limits to growth of forest biomass carbon sink under climate change. Nature Communications 9(1), 2709 (2018).
Bobbink, R., Ashmore, M., Braun, S., Flückiger, W., & Van den Wyngaert, I. J. Empirical nitrogen critical loads for natural and semi-natural ecosystems: 2002 update. Pages 43–107 in B. Achermann and R. Bobbick, editors. Empirical critical loads for nitrogen. Environmental Documentation Number 164. Swiss Agency for the Environment, Forests, and Landscape, Berne, Switzerland (2003).
Pardo, L. H. et al. Effects of nitrogen deposition and empirical nitrogen critical loads for ecoregions of the United States. Ecological Applications 21(8), 3049–3082 (2011).
Cárate‐Tandalla, D., Camenzind, T., Leuschner, C. & Homeier, J. Contrasting species responses to continued nitrogen and phosphorus addition in tropical montane forest tree seedlings. Biotropica 50(2), 234–245 (2018).
Reay, D. S., Dentener, F., Smith, P., Grace, J. & Feely, R. A. Global nitrogen deposition and carbon sinks. Nature Geoscience 1(7), 430 (2008).
Turner, B. L., Brenes-Arguedas, T. & Condit, R. Pervasive phosphorus limitation of tree species but not communities in tropical forests. Nature 555(7696), 367 (2018).
Arora, V. K. et al. Carbon–concentration and carbon–climate feedbacks in CMIP5 Earth system models. Journal of Climate 26(15), 5289–5314 (2013).
Guanter, L. et al. Global and time-resolved monitoring of crop photosynthesis with chlorophyll fluorescence. Proceedings of the National Academy of Sciences 111(14), E1327–E1333 (2014).
Zhang, Y., Song, C., Band, L. E. & Sun, G. No proportional increase of terrestrial gross carbon sequestration from the greening Earth. Journal of Geophysical Research: Biogeosciences 124(8), 2540–2553 (2019).
Lawrence, D. M. et al. The Community Land Model version 5: Description of new features, benchmarking, and impact of forcing uncertainty. Journal of Advances in Modeling Earth Systems (2019).
Fisher, J. B., Huntzinger, D. N., Schwalm, C. R. & Sitch, S. Modeling the terrestrial biosphere. Annual Review of Environment and Resources 39, 91–123 (2014).
Fisher, R. A., & Koven, C. D. Perspectives on the future of Land Surface Models and the challenges of representing complex terrestrial systems. Journal of Advances in Modeling Earth Systems (2020).
Pongratz, J. et al. Models meet data: Challenges and opportunities in implementing land management in Earth system models. Global Change Biology 24(4), 1470–1487 (2018).
Zhang, Q., Wang, Y. P., Matear, R. J., Pitman, A. J. & Dai, Y. J. Nitrogen and phosphorous limitations significantly reduce future allowable CO2 emissions. Geophysical Research Letters 41(2), 632–637 (2014).
Wei, Y. et al. The North American Carbon Program Multi-scale Synthesis and Terrestrial Model Intercomparison Project–Part 2: Environmental driver data. Geoscientific Model. Development 7(6), 2875–2893 (2014).
Phillips, T. J., Bonfils, C. J. & Zhang, C. Model consensus projections of US regional hydroclimates under greenhouse warming. Environmental Research Letters 14(1), 014005 (2019).
Knutti, R. The end of model democracy? Climatic Change 102, 395–404 (2010).
Bishop, C. H. & Abramowitz, G. Climate model dependence and the replicate Earth paradigm. Climate dynamics 41(3-4), 885–900 (2013).
Haughton, N., Abramowitz, G., Pitman, A. & Phipps, S. J. On the generation of climate model ensembles. Climate dynamics 43(7-8), 2297–2308 (2014).
Schwalm, C. R. et al. Toward “optimal” integration of terrestrial biosphere models. Geophys. Res. Lett. 42, 4418–4428, https://doi.org/10.1002/2015GL064002 (2015).
Liaw, A. & Wiener, M. Classification and regression by randomForest. R news, 373 2(3), 18–22 (2002).
CRS was supported by National Aeronautics and Space Administration (NASA) awards N4-TE14-0047-NNH14ZDA001N-TE, 13-CARBON13_2-0036-NNH13ZDA001N-CARBON and 14-CMAC14-NNX16AB19G. Funding for the Multi-scale synthesis and Terrestrial Model Intercomparison Project (MsTMIP; http://nacp.ornl.gov/MsTMIP.shtml) activity was provided through NASA ROSES Grant #NNX10AG01A. Data management support for preparing, documenting, and distributing model driver and output data was performed by the Modeling and Synthesis Thematic Data Center at Oak Ridge National Laboratory (ORNL; http://nacp.ornl.gov), with funding through NASA ROSES Grant #NNH10AN681. Finalized MsTMIP data products are archived at the ORNL DAAC (http://daac.ornl.gov). We also acknowledge the modeling groups that provided results to MsTMIP. For CMIP5, we acknowledge the World Climate Research Programme’s Working Group on Coupled Modelling, which is responsible for CMIP, and we thank the climate modeling groups for producing and making available their model output. For CMIP the U.S. Department of Energy’s Program for Climate Model Diagnosis and Intercomparison provides coordinating support and led development of software infrastructure in partnership with the Global Organization for Earth System Science Portals. JBF contributed to this research at the Jet Propulsion Laboratory, California Institute of Technology, under a contract with the National Aeronautics and Space Administration. California Institute of Technology. Government sponsorship acknowledged. JBF was supported in part by NASA programs: CARBON, CMS, IDS, and INCA. Copyright 2020. All rights reserved.
The authors declare no competing interests.
Publisher’s note Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.
About this article
Cite this article
Schwalm, C.R., Huntzinger, D.N., Michalak, A.M. et al. Modeling suggests fossil fuel emissions have been driving increased land carbon uptake since the turn of the 20th Century. Sci Rep 10, 9059 (2020). https://doi.org/10.1038/s41598-020-66103-9
This article is cited by
Ectomycorrhizal access to organic nitrogen mediates CO2 fertilization response in a dominant temperate tree
Nature Communications (2021)