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Abstract Digital leaf physiognomy (DLP) is considered as one of the most promising methods for estimating past climate. However, current models built using the DLP data set still lack precision, especially for mean annual precipitation (MAP). To improve predictive power, we developed five machine learning (ML) models for mean annual temperature (MAT) and MAP respectively, and then tested the precision of these models and some of their averaging compared with that obtained from other models. The precision of all models was assessed using a repeated stratified 10‐fold cross‐validation. For MAT, three combinations of models ( R 2 = .77) presented moderate improvements in precision over the multiple linear regression (MLR) model ( R 2 = .68). For log e (MAP), the averaging of the support vector machine (SVM) and boosting models improved the R 2 from .19 to .63 compared with that of the MLR model. For MAP, the R 2 of this model combination was 0.49, which was much better than that of the artificial neural network (ANN) model ( R 2 = .21). Even the bagging model, which had the lowest R 2 (.37) for log e (MAP), demonstrated better precision ( R 2 = .27) for MAP. Our palaeoclimate estimates for nine fossil floras were also more accurate, because they were in better agreement with independent paleoclimate evidence. Our study confirms that our ML models and their averaging can improve paleoclimatic reconstructions, providing a better understanding of the relationship between climate and leaf physiognomy.

Paleobotanists have long built leaf climate models based on site mean of leaf physiognomic characteristics of woody dicotyledons species (WDS) for estimating past climate. To explore the potential of the order Ericales in estimating paleoclimate, we developed two linear models for each climatic factor. One is based on WDS, and the other is based on both WDS and leaf physiognomic characters of the order Ericales (WDS-E). We found that, compared with WDS models, WDS-E models improved greatly in mean annual precipitation (MAP), growing season precipitation (GSP) and mean annual range in temperature (MART). When the minimum species number of the order Ericales is three per site, the WDS-E models improved the r2 from 0.64 to 0.78 for MART, from 0.23 to 0.61 for ln(MAP), and from 0.37 to 0.64 for ln(GSP) compared with the WDS models. For mean annual temperature (MAT), the WDS-E model (r2 = 0.86) also exhibited a moderate improvement in precision over the WDS model (r2 = 0.82). This study demonstrates that other patterns, such as those of the order Ericales, can contribute additional information towards building more precise paleoclimate models.

Paleobotanists have long built leaf climate models based on site mean of leaf physiognomic characteristics of woody dicotyledons species (WDS) for estimating past climate. To explore the potential of the order Ericales in estimating paleoclimate, we developed two linear models for each climatic factor. One is based on WDS, and the other is based on both WDS and leaf physiognomic characters of the order Ericales (WDS-E). We found that, compared with WDS models, WDS-E models improved greatly in mean annual precipitation (MAP), growing season precipitation (GSP) and mean annual range in temperature (MART). When the minimum species number of the order Ericales is three per site, the WDS-E models improved the r2 from 0.64 to 0.78 for MART, from 0.23 to 0.61 for ln(MAP), and from 0.37 to 0.64 for ln(GSP) compared with the WDS models. For mean annual temperature (MAT), the WDS-E model (r2 = 0.86) also exhibited a moderate improvement in precision over the WDS model (r2 = 0.82). This study demonstrates that other patterns, such as those of the order Ericales, can contribute additional information towards building more precise paleoclimate models.

Abstract Digital leaf physiognomy (DLP) is considered as one of the most promising methods for estimating past climate. However, current models built using the DLP data set still lack precision, especially for mean annual precipitation (MAP). To improve predictive power, we developed five machine learning (ML) models for mean annual temperature (MAT) and MAP respectively, and then tested the precision of these models and some of their averaging compared with that obtained from other models. The precision of all models was assessed using a repeated stratified 10‐fold cross‐validation. For MAT, three combinations of models ( R 2 = .77) presented moderate improvements in precision over the multiple linear regression (MLR) model ( R 2 = .68). For log e (MAP), the averaging of the support vector machine (SVM) and boosting models improved the R 2 from .19 to .63 compared with that of the MLR model. For MAP, the R 2 of this model combination was 0.49, which was much better than that of the artificial neural network (ANN) model ( R 2 = .21). Even the bagging model, which had the lowest R 2 (.37) for log e (MAP), demonstrated better precision ( R 2 = .27) for MAP. Our palaeoclimate estimates for nine fossil floras were also more accurate, because they were in better agreement with independent paleoclimate evidence. Our study confirms that our ML models and their averaging can improve paleoclimatic reconstructions, providing a better understanding of the relationship between climate and leaf physiognomy.

Abstract Biomass has been promoted as a promising energy resource to mitigate global climate change. To evaluate the contribution of biomass utilization to climate change mitigation under the “Grain for Green” program in Northern Shaanxi, China, a soil carbon dynamic model and a life cycle assessment model were integrated to examine the benefits of using Caragana korshinskii Kom. as an energy crop. We found that the annual dry biomass output is maintained at 0.7 Tg during the simulation period (2020–2097). Due to the compensatory effect of biomass regrowth, the global warming potential of biomass‐derived CO 2 emissions is approximately 0.045; therefore, the total annual biogenic CO 2 emission is 57,211 ± 6,168 Mg CO 2 eq. The total annual life cycle CO 2 emissions approach 867,072 Mg CO 2 eq yr −1 . Under the scenario of no biomass removal, final carbon storage ranges from 15.7 to 19.3 TgC, and the highest carbon sequestration rate is 0.47 TgC yr −1 . In comparison with the no biomass removal scenario, the carbon sequestration rate (close to 0 MgC yr −1 ) in the biomass utilization scenario indicates a carbon loss; however, a portion of the carbon loss (31.39–62.09%) can be offset by carbon emission reductions from the substitution of fossil fuels.

Wetlands are an important natural source of methane (CH4), so it is important to quantify how their emissions may vary under future climate change conditions. The Qinghai–Tibet Plateau contains more than a third of China’s wetlands. Here, we simulated temporal and spatial variation in CH4 emissions from natural wetlands on the Qinghai–Tibet Plateau from 2008 to 2100 under Representative Concentration Pathways (RCP) 2.6, 4.5, and 8.5. Based on the simulation results of the TRIPLEX-GHG model forced with data from 24 CMIP5 models of global climate, we predict that, assuming no change in wetland distribution on the Plateau, CH4 emissions from natural wetlands will increase by 35%, 98% and 267%, respectively, under RCP 2.6, 4.5 and 8.5. The predicted increase in atmospheric CO2 concentration will contribute 10–28% to the increased CH4 emissions from wetlands on the Plateau by 2100. Emissions are predicted to be majorly in the range of 0 to 30.5 g C m−2·a−1 across the Plateau and higher from wetlands in the southern region of the Plateau than from wetlands in central or northern regions. Under RCP8.5, the methane emissions of natural wetlands on the Qinghai–Tibet Plateau increased much more significantly than that under RCP2.6 and RCP4.5.

Phosphorus (P) is a key and a limiting nutrient in ecosystems and plays an important role in many physiological and biochemical processes, affecting both terrestrial ecosystem productivity and soil carbon storage. However, only a few global land surface models have incorporated P cycle and used to investigate the interactions of C-N-P and its limitation on terrestrial ecosystems. The overall objective of this study was to integrate the P cycle and its interaction with carbon (C) and nitrogen (N) into new processes model of TRIPLEX-CNP. In this study, key processes of the P cycle, including P pool sizes and fluxes in plant, litter, and soil were integrated into a new model framework, TRIPLEX-CNP. We also added dynamic P:C ratios for different ecosystems. Based on sensitivity analysis results, we identified the phosphorus resorption coefficient of leaf (rpleaf) as the most influential parameter to gross primary productivity (GPP) and biomass, and determined optimal coefficients for different plant functional types (PFTs). TRIPLEX-CNP was calibrated with 49 sites and validated against 116 sites across eight biomes globally. The results suggested that TRIPLEX-CNP performed well on simulating the global GPP and soil organic carbon (SOC) with respective R2 values of 0.85 and 0.78 (both p < 0.01) between simulated and observed values. The R2 of simulation and observation of total biomass are 0.67 (p < 0.01) by TRIPLEX-CNP. The overall model performance had been improved in global GPP, total biomass and SOC after adding the P cycle comparing with the earlier version. Our work represents the promising step toward new coupled ecosystem process models for improving the quantifications of land carbon cycle and reducing uncertainty.

Phosphorus (P) is a key and a limiting nutrient in ecosystems and plays an important role in many physiological and biochemical processes, affecting both terrestrial ecosystem productivity and soil carbon storage. However, only a few global land surface models have incorporated P cycle and used to investigate the interactions of C-N-P and its limitation on terrestrial ecosystems. The overall objective of this study was to integrate the P cycle and its interaction with carbon (C) and nitrogen (N) into new processes model of TRIPLEX-CNP. In this study, key processes of the P cycle, including P pool sizes and fluxes in plant, litter, and soil were integrated into a new model framework, TRIPLEX-CNP. We also added dynamic P:C ratios for different ecosystems. Based on sensitivity analysis results, we identified the phosphorus resorption coefficient of leaf (rpleaf) as the most influential parameter to gross primary productivity (GPP) and biomass, and determined optimal coefficients for different plant functional types (PFTs). TRIPLEX-CNP was calibrated with 49 sites and validated against 116 sites across eight biomes globally. The results suggested that TRIPLEX-CNP performed well on simulating the global GPP and soil organic carbon (SOC) with respective R2 values of 0.85 and 0.78 (both p < 0.01) between simulated and observed values. The R2 of simulation and observation of total biomass are 0.67 (p < 0.01) by TRIPLEX-CNP. The overall model performance had been improved in global GPP, total biomass and SOC after adding the P cycle comparing with the earlier version. Our work represents the promising step toward new coupled ecosystem process models for improving the quantifications of land carbon cycle and reducing uncertainty.

Wetlands are an important natural source of methane (CH4), so it is important to quantify how their emissions may vary under future climate change conditions. The Qinghai–Tibet Plateau contains more than a third of China’s wetlands. Here, we simulated temporal and spatial variation in CH4 emissions from natural wetlands on the Qinghai–Tibet Plateau from 2008 to 2100 under Representative Concentration Pathways (RCP) 2.6, 4.5, and 8.5. Based on the simulation results of the TRIPLEX-GHG model forced with data from 24 CMIP5 models of global climate, we predict that, assuming no change in wetland distribution on the Plateau, CH4 emissions from natural wetlands will increase by 35%, 98% and 267%, respectively, under RCP 2.6, 4.5 and 8.5. The predicted increase in atmospheric CO2 concentration will contribute 10–28% to the increased CH4 emissions from wetlands on the Plateau by 2100. Emissions are predicted to be majorly in the range of 0 to 30.5 g C m−2·a−1 across the Plateau and higher from wetlands in the southern region of the Plateau than from wetlands in central or northern regions. Under RCP8.5, the methane emissions of natural wetlands on the Qinghai–Tibet Plateau increased much more significantly than that under RCP2.6 and RCP4.5.

Intense and frequent drought events strongly affect plant survival. Non-structural carbohydrates (NSCs) are important “buffers” to maintain plant functions under drought conditions. We conducted a drought manipulation experiment using three-year-old Pinus tabulaeformis Carr. seedlings. The seedlings were first treated under different drought intensities (i.e., no irrigation, severe, and moderate) for 50 days, and then they were re-watered for 25 days to explore the dynamics of NSCs in the leaves, twigs, stems, and roots. The results showed that the no irrigation and severe drought treatments significantly reduced photosynthetic rate by 93.9% and 32.6% for 30 days, respectively, leading to the depletion of the starch storage for hydraulic repair, osmotic adjustment, and plant metabolism. The seedlings under moderate drought condition also exhibited starch storage consumption in leaves and twigs. After re-watering, the reduced photosynthetic rate recovered to the control level within five days in the severe drought group but showed no sign of recovery in the no irrigation group. The seedlings under the severe and moderate drought conditions tended to invest newly fixed C to starch storage and hydraulic repair instead of growth due to the “drought legacy effect”. Our findings suggest the depletion and recovery of starch storage are important strategies for P. tabulaeformis seedlings, and they may play key roles in plant resistance and resilience under environmental stress.

The 2001–2012 MODIS MCD12Q1 land cover data and MOD17A3 NPP data were used to calculate changes in land cover in China and annual changes in net primary productivity (NPP) during a 12-year period and to quantitatively analyze the effects of land cover change on the NPP of China’s terrestrial ecosystems. The results revealed that during the study period, no changes in land cover type occurred in 7447.31 thousand km2 of China, while the area of vegetation cover increased by 160.97 thousand km2 in the rest of the country. Forest cover increased to 20.91%, which was mainly due to the conversion of large areas of savanna (345.19 thousand km2) and cropland (178.96 thousand km2) to forest. During the 12-year study period, the annual mean NPP of China was 2.70 PgC and increased by 0.25 PgC, from 2.50 to 2.75 PgC. Of this change, 0.21 PgC occurred in areas where there was no land cover change, while 0.04 PgC occurred in areas where there was land cover change. The contributions of forest and cropland to NPP exhibited increasing trends, while the contributions of shrubland and grassland to NPP decreased. Among these land cover types, the contributions of forest and cropland to the national NPP were the greatest, accounting for 40.97% and 27.95%, respectively, of the annual total NPP. There was no significant correlation between changes in forest area and changes in total annual NPP (R2 < 0.1), while the correlation coefficient for changes in cropland area and total annual NPP was 0.48. Additionally, the area of cropland converted to other land cover types was negatively correlated with the changes in NPP, and the loss of cropland caused a reduction in the national NPP.

Few studies have focused on the combined impact of climate change, CO2, and land-use cover change (LUCC), especially the evaluation of the impact of LUCC on net primary productivity (NPP) in the future. In this study, we simulated the overall NPP change trend from 2010 to 2100 and its response to climatic factors, CO2 concentration, and LUCC conditions under three typical emission scenarios (Representative Concentration Pathway RCP2.6, RCP4.5, and RCP8.5). (1) Under the predicted global pattern, NPP showed an increasing trend, with the most prominent variation at the end of the century. The increasing trend is mainly caused by the positive effect of CO2 on NPP. However, the increasing trend of LUCC has only a small positive effect. (2) Under the RCP 8.5 scenario, from 2090 to 2100, CO2 has the most significant positive impact on tropical areas, reaching 8.328 Pg C Yr−1. Under the same conditions, climate change has the greatest positive impact on the northern high latitudes (1.175 Pg C Yr−1), but it has the greatest negative impact on tropical areas, reaching −4.842 Pg C Yr−1. (3) The average contribution rate of LUCC to NPP was 6.14%. Under the RCP8.5 scenario, LUCC made the largest positive contribution on NPP (0.542 Pg C Yr−1) globally from 2010 to 2020.