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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.

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 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.

Climate change is likely to lead to an increased frequency of droughts and floods, both of which are implicated in large-scale carbon allocation and tree mortality worldwide. Non-structural carbohydrates (NSCs) play an important role in tree survival under stress, but how NSC allocation changes in response to drought or waterlogging is still unclear. We measured soluble sugars (SS) and starch in leaves, twigs, stems and roots of Robinia pseudoacacia L. seedlings that had been subjected to a gradient in soil water availability from extreme drought to waterlogged conditions for a period of 30 days. Starch concentrations decreased and SS concentrations increased in tissues of R. pseudoacacia seedlings, such that the ratio of SS to starch showed a progressive increase under both drought and waterlogging stress. The strength of the response is asymmetric, with the largest increase occurring under extreme drought. While the increase in SS concentration in response to extreme drought is the largest in roots, the increase in the ratio of SS to starch is the largest in leaves. Individual components of SS showed different responses to drought and waterlogging across tissues: glucose concentrations increased significantly with drought in all tissues but showed little response to waterlogging in twigs and stems; sucrose and fructose concentrations showed marked increases in leaves and roots in response to drought but a greater response to drought and waterlogging in stems and twigs. These changes are broadly compatible with the roles of individual SS under conditions of water stress. While it is important to consider the role of NSC in buffering trees against mortality under stress, modelling this behaviour is unlikely to be successful unless it accounts for different responses within organs and the type of stress involved.

Methane accounts for 20% of the global warming caused by greenhouse gases, and wastewater is a major anthropogenic source of methane. Based on the Intergovernmental Panel on Climate Change greenhouse gas inventory guidelines and current research findings, we calculated the amount of methane emissions from 2000 to 2014 that originated from wastewater from different provinces in China. Methane emissions from wastewater increased from 1349.01 to 3430.03 Gg from 2000 to 2014, and the mean annual increase was 167.69 Gg. The methane emissions from industrial wastewater treated by wastewater treatment plants ( E It ) accounted for the highest proportion of emissions. We also estimated the future trend of industrial wastewater methane emissions using the artificial neural network model. A comparison of the emissions for the years 2020, 2010, and 2000 showed an increasing trend in methane emissions in China and a spatial transition of industrial wastewater emissions from eastern and southern regions to central and southwestern regions and from coastal regions to inland regions. These changes were caused by changes in economics, demographics, and relevant policies. , Key Points Methane emission from wastewater from 2000 to 2014 was calculated to increase from 1349.01 Gg to 3430.03 Gg. Methane emission from wastewater from 2015 to 2020 was estimated to increase from 3875.30 Gg to 5212.75 Gg. A spatial transition of methane emission from wastewater was found and discussed in the present study.