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Abstract Global rivers and streams are important carbon transport pathways from land to the ocean. However, few studies have quantified terrigenous carbon dynamics in river ecosystems and its variations due to climate change and anthropogenic perturbations. Therefore, our study analysed fluvial particulate organic carbon (POC) and developed a processed‐based model (TRIPLEX‐HYDRA) to simulate the production, transport and removal (i.e., deposition, degradation and dam retention) processes of fluvial POC along the land–ocean aquatic continuum (LOAC). Based on our results, approximately 0.29 Pg of POC is exported from land to the ocean through rivers each year. More specifically, we found that rivers at low latitudes (30°S–30°N, 0.18 Pg yr −1 ) and high northern latitudes (60°N–90°N, 0.05 Pg yr −1 ) had higher POC fluxes compared to rivers in other regions. This high POC flux is related to strong erosion rates and high soil organic carbon storage. Additionally, our model simulation revealed that total POC flux from global river has not significantly changed from 1983 to 2015 but displays markedly decreased or increased trend at regional scale. These regional variations in POC export are affected by climate warming and dam construction. Moreover, approximately 0.46 Pg of POC is deposited or trapped by dams along the LOAC system, which plays a vital role in the global river carbon budget. Although some limitations and uncertainties remain, this study establishes a theoretical and methodological basis for quantifying riverine POC dynamics in the LOAC system.

Many hypotheses have been proposed to explain elevational species richness patterns; however, evaluating their importance remains a challenge, as mountains that are nested within different biogeographic regions have different environmental attributes. Here, we conducted a comparative study for trees, shrubs, herbs, and ferns along the same elevational gradient for 22 mountains worldwide, examining the performance of hypotheses of energy, tolerance, climatic variability, and spatial area to explain the elevational species richness patterns for each plant group. Results show that for trees and shrubs, energy-related factors exhibit greater explanatory power than other factors, whereas the factors that are associated with climatic variability performed better in explaining the elevational species richness patterns of herbs and ferns. For colder mountains, energy-related factors emerged as the main drivers of woody species diversity, whereas in hotter and wetter ecosystems, temperature and precipitation were the most important predictors of species richness along elevational gradients. For herbs and ferns, the variation in species richness was less than that of woody species. These findings provide important evidence concerning the generality of the energy theory for explaining the elevational species richness pattern of plants, highlighting that the underlying mechanisms may change among different growth form groups and regions within which mountains are nested.

Many hypotheses have been proposed to explain elevational species richness patterns; however, evaluating their importance remains a challenge, as mountains that are nested within different biogeographic regions have different environmental attributes. Here, we conducted a comparative study for trees, shrubs, herbs, and ferns along the same elevational gradient for 22 mountains worldwide, examining the performance of hypotheses of energy, tolerance, climatic variability, and spatial area to explain the elevational species richness patterns for each plant group. Results show that for trees and shrubs, energy-related factors exhibit greater explanatory power than other factors, whereas the factors that are associated with climatic variability performed better in explaining the elevational species richness patterns of herbs and ferns. For colder mountains, energy-related factors emerged as the main drivers of woody species diversity, whereas in hotter and wetter ecosystems, temperature and precipitation were the most important predictors of species richness along elevational gradients. For herbs and ferns, the variation in species richness was less than that of woody species. These findings provide important evidence concerning the generality of the energy theory for explaining the elevational species richness pattern of plants, highlighting that the underlying mechanisms may change among different growth form groups and regions within which mountains are nested.

Abstract Aim Compared with gradual climate change, extreme climatic events have more direct and dramatic impacts on vegetation growth. However, the influence of climate extremes on important phenological periods, such as the end of the growing season (EOS), remains unclear. Here, we investigate the temporal trends of EOS across different biomes and quantify the response of EOS to multiple climate extreme indices (CEIs). Location Northern middle and high latitudes. Time period 2000–2020. Major taxa studied Plants. Methods Three phenology extraction methods were used to compute EOS from satellite, FLUXNET and Pan European Phenology Project PEP725 phenological datasets. Different stress states of cold, hot, dry and wet extremes were represented by 12 CEIs. Partial correlation and ridge regression analysis were used to quantify the response of EOS to climate extremes across latitudinal and biome scales. Results Our study showed a delayed EOS in boreal biomes, but a significantly advanced EOS in temperate biomes. The advanced EOS induced by cold stress was observed for c . 80% of the vegetated pixels. The warm‐related CEIs delayed the EOS in high latitudes, and the delayed effect weakened or even reversed with decreasing latitude. In contrast, EOS exhibited opposite response patterns to dry days and wet‐related CEIs. Overall, EOS exhibited higher sensitivity to extreme temperature in boreal biomes than in temperate biomes. Specifically, continuous drought and high heat stress induced an earlier EOS in some temperate forest biomes, whereas moderate heat stress delayed the EOS in most study biomes. In contrast, EOS was not sensitive to extreme drought in water‐restricted biomes. Main conclusions EOS exhibited divergent responses to various climate extremes with different intensities and frequencies. Moreover, the response of EOS to extreme climate stress was dependent on the biome and latitude. These findings emphasize the importance of incorporating the divergent extreme climate effects into vegetation phenological models and Earth system models.

Understanding the biomass, characteristics, and carbon sequestration of urban forests is crucial for maintaining and improving the quality of life and ensuring sustainable urban planning. Approaches to urban forest management have been incorporated into interdisciplinary, multifunctional, and technical efforts. In this review, we evaluate recent developments in urban forest research methods, compare the accuracy and efficiency of different methods, and identify emerging themes in urban forest assessment. This review focuses on urban forest biomass estimation and individual tree feature detection, showing that the rapid development of remote sensing technology and applications in recent years has greatly benefited the study of forest dynamics. Included in the review are light detection and ranging-based techniques for estimating urban forest biomass, deep learning algorithms that can extract tree crowns and identify tree species, methods for measuring large canopies using unmanned aerial vehicles to estimate forest structure, and approaches for capturing street tree information using street view images. Conventional methods based on field measurements are highly beneficial for accurately recording species-specific characteristics. There is an urgent need to combine multi-scale and spatiotemporal methods to improve urban forest detection at different scales.

Urban ecosystems are complex systems with anthropogenic features that generate considerable CO 2 emissions, which contributes to global climate change. Quantitative estimates of the carbon footprint of urban ecosystems are crucial for developing low-carbon development policies to mitigate climate change. Herein, we reviewed more than 195 urban carbon footprint and carbon footprint related studies, collated the recent progress in carbon footprint calculation methods and research applications of the urban ecosystem carbon footprint, analyzed the research applications of the carbon footprint of different cities, and focused on the need to study the urban ecosystem carbon footprint from a holistic perspective. Specifically, we aimed to: (i) compare the strengths and weaknesses of five existing carbon footprint calculation methods [life cycle assessment, input–output analysis, hybrid life cycle assessment, carbon footprint calculator, and Intergovernmental Panel on Climate Change (IPCC)]; (ii) analyze the status of current research on the carbon footprint of different urban subregions based on different features; and (iii) highlight new methods and areas of research on the carbon footprint of future urban ecosystems. Not all carbon footprint accounting methods are applicable to the carbon footprint determination of urban ecosystems; although the IPCC method is more widely used than the others, the hybrid life cycle assessment method is more accurate. With the emergence of new science and technology, quantitative methods to calculate the carbon footprint of urban ecosystems have evolved, becoming more accurate. Further development of new technologies, such as big data and artificial intelligence, to assess the carbon footprint of urban ecosystems is anticipated to help address the emerging challenges in urban ecosystem research effectively to achieve carbon neutrality and urban sustainability under global change.

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.

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.

Abstract Aim Plant biomass allocation reflects the distribution of photosynthates among different organs in response to changing environmental conditions. Global change influences plant growth across terrestrial ecosystems, but impacts of individual and combined multiple global change factors (GCFs) on plant biomass allocation at the global scale are unclear. Location Global. Time period Contemporary. Major taxa studied Plants in terrestrial ecosystems. Methods We conducted a meta‐analysis of data comprising 4,180 pairwise observations to assess individual and combined effects of nitrogen addition (N), warming (W), elevated CO 2 (C), irrigation (I), and drought (D) on plant biomass allocation based on the ‘ratio‐based optimal partitioning’ and ‘isometric allocation’ hypotheses. Results We found that (a) ratio‐based plant biomass fractions of different organs were only minimally affected by individual and combined effects of the studied GCFs; (b) combined effects of two‐factor pairs of GCFs on plant biomass allocation were commonly additive, rather than synergistic or antagonistic; (c) moderator variables influenced, but seldom changed the direction of individual and combined effects of GCFs on plant biomass allocation; and (d) neither individual nor combined effects of the studied GCFs altered allometric relationships among different organs, indicating that patterns of plant biomass allocation under the environmental stress conditions exerted by the multiple GCFs were better explained by the isometric allocation rather than the ratio‐based optimal partitioning hypothesis. Main conclusions Our results show consistent patterns of allometric plant biomass partitioning under effects of multiple GCFs and provide evidence of an isometric plant biomass allocation trajectory in response to global change perturbations. These findings improve our understanding and prediction of terrestrial vegetation responses to future global change scenarios.