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Nitrous oxide (N2O), like carbon dioxide, is a long-lived greenhouse gas that accumulates in the atmosphere. Over the past 150 years, increasing atmospheric N2O concentrations have contributed to stratospheric ozone depletion1 and climate change2, with the current rate of increase estimated at 2 per cent per decade. Existing national inventories do not provide a full picture of N2O emissions, owing to their omission of natural sources and limitations in methodology for attributing anthropogenic sources. Here we present a global N2O inventory that incorporates both natural and anthropogenic sources and accounts for the interaction between nitrogen additions and the biochemical processes that control N2O emissions. We use bottom-up (inventory, statistical extrapolation of flux measurements, process-based land and ocean modelling) and top-down (atmospheric inversion) approaches to provide a comprehensive quantification of global N2O sources and sinks resulting from 21 natural and human sectors between 1980 and 2016. Global N2O emissions were 17.0 (minimum-maximum estimates: 12.2-23.5) teragrams of nitrogen per year (bottom-up) and 16.9 (15.9-17.7) teragrams of nitrogen per year (top-down) between 2007 and 2016. Global human-induced emissions, which are dominated by nitrogen additions to croplands, increased by 30% over the past four decades to 7.3 (4.2-11.4) teragrams of nitrogen per year. This increase was mainly responsible for the growth in the atmospheric burden. Our findings point to growing N2O emissions in emerging economies-particularly Brazil, China and India. Analysis of process-based model estimates reveals an emerging N2O-climate feedback resulting from interactions between nitrogen additions and climate change. The recent growth in N2O emissions exceeds some of the highest projected emission scenarios3,4, underscoring the urgency to mitigate N2O emissions.
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Óxido Nitroso/análise , Óxido Nitroso/metabolismo , Agricultura , Atmosfera/química , Produtos Agrícolas/metabolismo , Atividades Humanas , Internacionalidade , Nitrogênio/análise , Nitrogênio/metabolismoRESUMO
Nitrous oxide (N2O) is a long-lived greenhouse gas and currently contributes â¼10% to global greenhouse warming. Studies have suggested that inland waters are a large and growing global N2O source, but whether, how, where, when, and why inland-water N2O emissions changed in the Anthropocene remains unclear. Here, we quantify global N2O formation, transport, and emission along the aquatic continuum and their changes using a spatially explicit, mechanistic, coupled biogeochemistry-hydrology model. The global inland-water N2O emission increased from 0.4 to 1.3 Tg N yr-1 during 1900-2010 due to (1) growing N2O inputs mainly from groundwater and (2) increased inland-water N2O production, largely in reservoirs. Inland waters currently contribute 7 (5-10)% to global total N2O emissions. The highest inland-water N2O emissions are typically in and downstream of reservoirs and areas with high population density and intensive agricultural activities in eastern and southern Asia, southeastern North America, and Europe. The expected continuing excessive use of nutrients, dam construction, and development of suboxic conditions in aging reservoirs imply persisting high inland-water N2O emissions.
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Agricultura , Óxido Nitroso , Ásia Meridional , ÁguaRESUMO
Rivers play an important role in the global carbon (C) cycle. However, it remains unknown how long-term river C fluxes change because of climate, land-use, and other environmental changes. Here, we investigated the spatiotemporal variations in global freshwater C cycling in the 20th century using the mechanistic IMAGE-Dynamic Global Nutrient Model extended with the Dynamic In-Stream Chemistry Carbon module (DISC-CARBON) that couples river basin hydrology, environmental conditions, and C delivery with C flows from headwaters to mouths. The results show heterogeneous spatial distribution of dissolved inorganic carbon (DIC) concentrations in global inland waters with the lowest concentrations in the tropics and highest concentrations in the Arctic and semiarid and arid regions. Dissolved organic carbon (DOC) concentrations are less than 10 mg C/L in most global inland waters and are generally high in high-latitude basins. Increasing global C inputs, burial, and CO2 emissions reported in the literature are confirmed by DISC-CARBON. Global river C export to oceans has been stable around 0.9 Pg yr-1. The long-term changes and spatial patterns of concentrations and fluxes of different C forms in the global river network unfold the combined influence of the lithology, climate, and hydrology of river basins, terrestrial and biological C sources, in-stream C transformations, and human interferences such as damming.
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Matéria Orgânica Dissolvida , Rios , Regiões Árticas , Água Doce , Humanos , HidrologiaRESUMO
As Chinese aquaculture production accounts for over half of the global aquaculture production and has increased by 50% since 2006, there is growing concern about eutrophication caused by aquaculture in China. This paper presents a model-based estimate of nutrient flows in China's aquaculture system during 2006-2017 using provincial scale data, to spatially distribute nutrient loads with a 0.5° resolution. The results indicate that with the increase in fish and shellfish production from 30 to 47 million tonnes (Mt) during 2006-2017, the nitrogen (N) release increased from 1.0 to 1.6 Mt/year and that of phosphorus (P) from 0.1 to 0.2 Mt/year. Nutrient release from freshwater aquaculture was concentrated in Guangdong, Jiangsu, and Hubei, and that from mariculture in Shandong, Fujian, and Guangdong. Aquaculture is an important strongly concentrated nutrient source in both freshwater and marine environments. Its nutrient release is >20% of total nutrient inputs to freshwater environments in some provinces, and nutrients from mariculture are comparable to river nutrient export to Chinese coastal seas. Aquaculture production and nutrient excretions are now comparable to those of livestock production systems in China and need to be accounted for when analyzing causes of eutrophication and harmful algal blooms and possible mitigation strategies.
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Aquicultura , Água Doce , Animais , China , Monitoramento Ambiental , Eutrofização , Nitrogênio , Nutrientes , Oceanos e Mares , FósforoRESUMO
This paper presents the spatially explicit (0.5° spatial resolution) Dynamic InStream Chemistry (DISC)-SILICON module, which is part of the Integrated Model to Assess the Global Environment-Dynamic Global Nutrient Model global nutrient cycling framework. This new model, for the first time, enables to integrate the combined impact of long-term changes in land use, climate, and hydrology on Si sources (weathering, sewage, and soil loss) and sinks (uptake by diatoms, sedimentation, and burial) along the river continuum. Comparison of discharge and dissolved silica results with observations shows good agreement both in the Rhine and Yangtze. The simulated total Si export for the Rhine is stable during the period 1900-2000. The total Si export for the Yangtze decreased (155-51 Gmol yr-1) because of damming and transformation of 40% of the natural vegetation to cropland. As a result of dam construction in the Yangtze, diatom primary production (from 24 to 48 Gmol yr-1) and burial (15 to 32 Gmol yr-1) increased and the DSi export decreased (139-46 Gmol yr-1) from the 1950s to 1990s. The Three Gorges Reservoir has a large contribution to diatom primary production (11%) and burial (12%) in the Yangtze basin. DISC-SILICON reproduces a flooding-induced increase in Si inputs and burial and the legacy of this temporary storage in subsequent dry years.
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Diatomáceas , Rios , China , Monitoramento Ambiental , Hidrologia , SilícioRESUMO
Understanding how cities can transform organic waste into a valuable resource is critical to urban sustainability. The capture and recycling of phosphorus (P), and other essential nutrients, from human excreta is particularly important as an alternative organic fertilizer source for agriculture. However, the complex set of socio-environmental factors influencing urban human excreta management is not yet sufficiently integrated into sustainable P research. Here, we synthesize information about the pathways P can take through urban sanitation systems along with barriers and facilitators to P recycling across cities. We examine five case study cities by using a sanitation chains approach: Accra, Ghana; Buenos Aires, Argentina; Beijing, China; Baltimore, USA; and London, England. Our cross-city comparison shows that London and Baltimore recycle a larger percentage of P from human excreta back to agricultural lands than other cities, and that there is a large diversity in socio-environmental factors that affect the patterns of recycling observed across cities. Our research highlights conditions that may be "necessary but not sufficient" for P recycling, including access to capital resources. Path dependencies of large sanitation infrastructure investments in the Global North contrast with rapidly urbanizing cities in the Global South, which present opportunities for alternative sanitation development pathways. Understanding such city-specific social and environmental barriers to P recycling options could help address multiple interacting societal objectives related to sanitation and provide options for satisfying global agricultural nutrient demand.
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Phosphorus (P) is a finite and dwindling resource. Debate focuses on current production and use of phosphate rock rather than on the amounts of P required in the future to feed the world. We applied a two-pool soil P model to reproduce historical continental crop P uptake as a function of P inputs from fertilizer and manure and to estimate P requirements for crop production in 2050. The key feature is the consideration of the role of residual soil P in crop production. Model simulations closely fit historical P uptake for all continents. Cumulative inputs of P fertilizer and manure for the period 1965-2007 in Europe (1,115 kg . ha(-1) of cropland) grossly exceeded the cumulative P uptake by crops (360 kg ha(-1)). Since the 1980s in much of Europe, P application rates have been reduced, and uptake continues to increase due to the supply of plant-available P from residual soil P pool. We estimate that between 2008 and 2050 a global cumulative P application of 700-790 kg . ha(-1) of cropland (in total 1,070-1,200 teragrams P) is required to achieve crop production according to the various Millennium Ecosystem Assessment scenarios [Alcamo J, Van Vuuren D, Cramer W (2006) Ecosystems and Human Well-Being: Scenarios, Vol 2, pp 279-354]. We estimate that average global P fertilizer use must change from the current 17.8 to 16.8-20.8 teragrams per year in 2050, which is up to 50% less than other estimates in the literature that ignore the role of residual soil P.
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Conservação dos Recursos Naturais/métodos , Produtos Agrícolas/metabolismo , Fósforo/análise , Solo/análise , Agricultura/métodos , Agricultura/tendências , Algoritmos , Animais , Conservação dos Recursos Naturais/tendências , Produtos Agrícolas/crescimento & desenvolvimento , Ecossistema , Europa (Continente) , Fertilizantes/análise , Previsões , Humanos , Esterco/análise , Modelos BiológicosRESUMO
Phosphorus (P) is an essential nutrient for algal growth in nearshore ecosystems. In recent years, there has been a shift in nutrient dynamics in nearshore areas, leading to an exacerbation of P limitation, although the underlying mechanisms remain unclear. This study analyzed the P species and budget in the Bohai Sea (BS) from 2011 to 2020, aiming to explore the intrinsic mechanisms of P limitation in the BS. The results show that the main external source of P in the BS was river transport (89%), and the primary fate of P was burial (96%) into the sediment. Due to excessive nitrogen (N) input and biological processes in the BS, the P budget in the BS is unbalanced, resulting in an increase in the N/P ratio, particularly in nearshore areas. Nearshore areas typically have lower concentrations of dissolved inorganic P (DIP) in the water and higher concentrations of reactive P (Reac-P) in the sediments. This pattern is particularly evident in Bohai Bay and the northwest nearshore region, where harmful algal blooms occur frequently. To cope with enhanced P limitation, the biologically driven P regeneration and cycling processes within the BS are accelerated. From 2011 to 2020, the concentration of DIP in the BS during autumn increased, while the content of Reac-P in sediments slightly decreased. Historical data indicate that P depletion in the BS is intensifying and expanding, primarily due to N enrichment and algal production. N enrichment alters the structure and composition of primary production, potentially exacerbating P depletion in the BS. Excessive N may have significant impacts on the P pool, potentially influencing the stability of future coastal ecosystems.
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Monitoramento Ambiental , Nitrogênio , Fósforo , Poluentes Químicos da Água , Fósforo/metabolismo , Nitrogênio/metabolismo , China , Poluentes Químicos da Água/análise , Poluentes Químicos da Água/metabolismo , Sedimentos Geológicos/química , Água do Mar/química , Ecossistema , Proliferação Nociva de AlgasRESUMO
Harmful algal blooms (HABs) have been increasing in frequency, areal extent and duration due to the large increase in nutrient inputs from land-based sources to coastal seas, and cause significant economic losses. In this study, we used the "watershed-coast-continuum" concept to explore the effects of land-based nutrient pollution on HAB development in the Eastern Chinese coastal seas (ECCS). Results from the coupling of a watershed nutrient model and a coast hydrodynamic-biogeochemical model show that between the 1980s and 2000s, the risk of diatom blooms and dinoflagellate blooms increased by 158% and 127%, respectively. The spatial expansion of HAB risk caused by dinoflagellates is larger than that of diatoms. The simulated suitability of the habitat for bloom of Aureococcus anophagefferens, a pico-plankton of non-diatom or dinoflagellate, in the Bohai Sea is consistent with observations spatially and temporally. To halt further nutrient accumulation in the ECCS, reductions of dissolved inorganic nitrogen (DIN) (16%) and dissolved inorganic phosphorus (DIP) (33%) loading are required. To improve the situation of distorted DIN:DIP ratios, even larger reductions of DIN are required, especially in the Bohai Sea. Our approach is a feasible way to predict the risk of HABs under the pressure of increasing anthropogenic nutrient pollution in coastal waters.
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Diatomáceas , Dinoflagellida , Proliferação Nociva de Algas , Nitrogênio/análise , Nutrientes , Oceanos e Mares , China , Poluição da ÁguaRESUMO
Agricultural N losses strongly dominate the N delivery (average 72 % of total N delivery to rivers in the period 1980-2010) in the rivers discharging into the Bohai Sea, a semi-enclosed marginal sea, which has been suffering from eutrophication and deoxygenation since the 1980s. In this paper we investigate the relationship between N loading and deoxygenation in the Bohai Sea, and consequences of future N loading scenarios. Using modeling for the period 1980-2010, the contributions of different oxygen consumption processes were quantified and the main controlling mechanisms of summer bottom dissolved oxygen (DO) evolution in the central Bohai Sea were determined. Model results show that the water column stratification during summer impeded the DO exchange between oxygenated surface water and oxygen-poor bottom water. Water column oxygen consumption (60 % of total oxygen consumption) was strongly correlated with elevated nutrient loading, while nutrient imbalances (increasing N:P ratios) enhanced harmful algal bloom proliferation. Future scenarios show that deoxygenation may be reduced in all scenarios owing to increasing agricultural efficiency, manure recycling and wastewater treatment. However, even in the sustainable development scenario SSP1, nutrient discharges in 2050 will still exceed the 1980 levels, and with further enhancement of water stratification due to climate warming, the risk of summer hypoxia in bottom waters may persist in the coming decades.
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Sub-Saharan Africa must urgently improve food security. Phosphorus availability is one of the major barriers to this due to low historical agricultural use. Shared socioeconomic pathways (SSPs) indicate that only a sustainable (SSP1) or a fossil fuelled future (SSP5) can improve food security (in terms of price, availability, and risk of hunger) whilst nationalistic (SSP3) and unequal (SSP4) pathways worsen food security. Furthermore, sustainable SSP1 requires limited cropland expansion and low phosphorus use whilst the nationalistic SSP3 is as environmentally damaging as the fossil fuelled pathway. The middle of the road future (SSP2) maintains today's inadequate food security levels only by using approximately 440 million tonnes of phosphate rock. Whilst this is within the current global reserve estimates the market price alone for a commonly used fertiliser (DAP) would cost US$ 130 ± 25 billion for agriculture over the period 2020 to 2050 and the farmgate price could be two to five times higher due to additional costs (e.g. transport, taxation etc.). Thus, to improve food security, economic growth within a sustainability context (SSP1) and the avoidance of nationalist ideology (SSP3) should be prioritised.
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Agricultura , Fósforo , África Subsaariana , Fertilizantes , Segurança Alimentar , Abastecimento de AlimentosRESUMO
Global projections indicate that approximately 500 Mha of new arable land will be required to meet crop demand by 2050. Applying a dynamic phosphorus (P) pool simulator under different socioeconomic scenarios, we find that cropland expansion can be avoided with less than 7% additional cumulative P fertilizer over 2006-2050 when comparing with cropland expansion scenarios, mostly targeted at nutrient-depleted soils of sub-Saharan Africa. Additional P fertilizer would replenish P withdrawn from crop production, thereby allowing higher productivity levels. We also show that further agronomic improvements such as those that allow for better (legacy) P use in soils could reduce both P outflows to freshwater and coastal ecosystems and the overall demand for P fertilizer.
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Mitigating soil nitrous oxide (N2O) emissions is essential for staying below a 2 °C warming threshold. However, accurate assessments of mitigation potential are limited by uncertainty and variability in direct emission factors (EFs). To assess where and why EFs differ, we created high-resolution maps of crop-specific EFs based on 1,507 georeferenced field observations. Here, using a data-driven approach, we show that EFs vary by two orders of magnitude over space. At global and regional scales, such variation is primarily driven by climatic and edaphic factors rather than the well-recognized management practices. Combining spatially explicit EFs with N surplus information, we conclude that global mitigation potential without compromising crop production is 30% (95% confidence interval, 17-53%) of direct soil emissions of N2O, equivalent to the entire direct soil emissions of China and the United States combined. Two-thirds (65%) of the mitigation potential could be achieved on one-fifth of the global harvested area, mainly located in humid subtropical climates and across gleysols and acrisols. These findings highlight the value of a targeted policy approach on global hotspots that could deliver large N2O mitigation as well as environmental and food co-benefits.
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Nitrogen (N) and phosphorus (P) flows from land to sea in the Yangtze River basin were simulated for the period 1900-2010, by combining models for hydrology, nutrient input to surface water, and an in-stream retention. This study reveals that the basin-wide nutrient budget, delivery to surface water, and in-stream retention increased during this period. Since 2004, the Three Gorges Reservoir has contributed 5% and 7% of N and P basin-wide retention, respectively. With the dramatic rise in nutrient delivery, even this additional retention was insufficient to prevent an increase of riverine export from 337â¯Ggâ¯N yr-1 and 58â¯Ggâ¯P yr-1 (N:P molar ratioâ¯=â¯13) to 5896â¯Ggâ¯N yr-1 and 381â¯Ggâ¯P yr-1 (N:P molar ratioâ¯=â¯35) to the East China Sea and Yellow Sea (ECSYS). The midstream and upstream subbasins dominate the N and P exports to the ECSYS, respectively, due to various human activities along the river. Our spatially explicit nutrient source allocation can aid in the strategic targeting of nutrient reduction policies. We posit that these should focus on improving the agricultural fertilizer and manure use efficiency in the upstream and midstream and better urban wastewater management in the downstream subbasin.
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Nitrogênio/análise , Fósforo/análise , Rios/química , Agricultura , China , Monitoramento Ambiental , Fertilizantes , Hidrologia/métodos , Oceanos e Mares , Análise Espaço-Temporal , Poluição da Água/análiseRESUMO
This study analyzes the influence of various fertilizer management practices on crop yield and soil organic carbon (SOC) based on the long-term field observations and modelling. Data covering 11â¯years from 8 long-term field trials were included, representing a range of typical soil, climate, and agro-ecosystems in China. The process-based model EPIC (Environmental Policy Integrated Climate model) was used to simulate the response of crop yield and SOC to various fertilization regimes. The results showed that the yield and SOC under additional manure application treatment were the highest while the yield under control treatment was the lowest (30%-50% of NPK yield) at all sites. The SOC in northern sites appeared more dynamic than that in southern sites. The variance partitioning analysis (VPA) showed more variance of crop yield could be explained by the fertilization factor (42%), including synthetic nitrogen (N), phosphorus (P), potassium (K) fertilizers, and fertilizer NPK combined with manure. The interactive influence of soil (total N, P, K, and available N, P, K) and climate factors (mean annual temperature and precipitation) determine the largest part of the SOC variance (32%). EPIC performs well in simulating both the dynamics of crop yield (NRMSEâ¯=â¯32% and 31% for yield calibration and validation) and SOC (NRMSEâ¯=â¯13% and 19% for SOC calibration and validation) under diverse fertilization practices in China. EPIC can assist in predicting the impacts of different fertilization regimes on crop growth and soil carbon dynamics, and contribute to the optimization of fertilizer management for different areas in China.
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Global nitrogen fixation contributes 413 Tg of reactive nitrogen (Nr) to terrestrial and marine ecosystems annually of which anthropogenic activities are responsible for half, 210 Tg N. The majority of the transformations of anthropogenic Nr are on land (240 Tg N yr(-1)) within soils and vegetation where reduced Nr contributes most of the input through the use of fertilizer nitrogen in agriculture. Leakages from the use of fertilizer Nr contribute to nitrate (NO3(-)) in drainage waters from agricultural land and emissions of trace Nr compounds to the atmosphere. Emissions, mainly of ammonia (NH3) from land together with combustion related emissions of nitrogen oxides (NOx), contribute 100 Tg N yr(-1) to the atmosphere, which are transported between countries and processed within the atmosphere, generating secondary pollutants, including ozone and other photochemical oxidants and aerosols, especially ammonium nitrate (NH4NO3) and ammonium sulfate (NH4)2SO4. Leaching and riverine transport of NO3 contribute 40-70 Tg N yr(-1) to coastal waters and the open ocean, which together with the 30 Tg input to oceans from atmospheric deposition combine with marine biological nitrogen fixation (140 Tg N yr(-1)) to double the ocean processing of Nr. Some of the marine Nr is buried in sediments, the remainder being denitrified back to the atmosphere as N2 or N2O. The marine processing is of a similar magnitude to that in terrestrial soils and vegetation, but has a larger fraction of natural origin. The lifetime of Nr in the atmosphere, with the exception of N2O, is only a few weeks, while in terrestrial ecosystems, with the exception of peatlands (where it can be 10(2)-10(3) years), the lifetime is a few decades. In the ocean, the lifetime of Nr is less well known but seems to be longer than in terrestrial ecosystems and may represent an important long-term source of N2O that will respond very slowly to control measures on the sources of Nr from which it is produced.