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  • 11
    Publication Date: 2022-06-17
    Repository Name: EPIC Alfred Wegener Institut
    Type: Article , notRev
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  • 12
    Publication Date: 2022-05-26
    Description: © The Author(s), 2018. This article is distributed under the terms of the Creative Commons Attribution License. The definitive version was published in Earth System Science Data 10 (2018): 405-448, doi:10.5194/essd-10-405-2018.
    Description: Accurate assessment of anthropogenic carbon dioxide (CO2) emissions and their redistribution among the atmosphere, ocean, and terrestrial biosphere – the "global carbon budget" – is important to better understand the global carbon cycle, support the development of climate policies, and project future climate change. Here we describe data sets and methodology to quantify the five major components of the global carbon budget and their uncertainties. CO2 emissions from fossil fuels and industry (EFF) are based on energy statistics and cement production data, respectively, while emissions from land-use change (ELUC), mainly deforestation, are based on land-cover change data and bookkeeping models. The global atmospheric CO2 concentration is measured directly and its rate of growth (GATM) is computed from the annual changes in concentration. The ocean CO2 sink (SOCEAN) and terrestrial CO2 sink (SLAND) are estimated with global process models constrained by observations. The resulting carbon budget imbalance (BIM), the difference between the estimated total emissions and the estimated changes in the atmosphere, ocean, and terrestrial biosphere, is a measure of imperfect data and understanding of the contemporary carbon cycle. All uncertainties are reported as ±1σ. For the last decade available (2007–2016), EFF was 9.4 ± 0.5 GtC yr−1, ELUC 1.3 ± 0.7 GtC yr−1, GATM 4.7 ± 0.1 GtC yr−1, SOCEAN 2.4 ± 0.5 GtC yr−1, and SLAND 3.0 ± 0.8 GtC yr−1, with a budget imbalance BIM of 0.6 GtC yr−1 indicating overestimated emissions and/or underestimated sinks. For year 2016 alone, the growth in EFF was approximately zero and emissions remained at 9.9 ± 0.5 GtC yr−1. Also for 2016, ELUC was 1.3 ± 0.7 GtC yr−1, GATM was 6.1 ± 0.2 GtC yr−1, SOCEAN was 2.6 ± 0.5 GtC yr−1, and SLAND was 2.7 ± 1.0 GtC yr−1, with a small BIM of −0.3 GtC. GATM continued to be higher in 2016 compared to the past decade (2007–2016), reflecting in part the high fossil emissions and the small SLAND consistent with El Niño conditions. The global atmospheric CO2 concentration reached 402.8 ± 0.1 ppm averaged over 2016. For 2017, preliminary data for the first 6–9 months indicate a renewed growth in EFF of +2.0 % (range of 0.8 to 3.0 %) based on national emissions projections for China, USA, and India, and projections of gross domestic product (GDP) corrected for recent changes in the carbon intensity of the economy for the rest of the world. This living data update documents changes in the methods and data sets used in this new global carbon budget compared with previous publications of this data set (Le Quéré et al., 2016, 2015b, a, 2014, 2013). All results presented here can be downloaded from https://doi.org/10.18160/GCP-2017 (GCP, 2017).
    Repository Name: Woods Hole Open Access Server
    Type: Article
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  • 13
    Publication Date: 2023-07-17
    Description: Accurate assessment of anthropogenic carbon dioxide (CO2) emissions and their redistribution among the atmosphere, ocean, and terrestrial biosphere in a changing climate is critical to better understand the global carbon cycle, support the development of climate policies, and project future climate change. Here we describe and synthesize data sets and methodologies to quantify the five major components of the global carbon budget and their uncertainties. Fossil CO2 emissions (EFOS) are based on energy statistics and cement production data, while emissions from land-use change (ELUC), mainly deforestation, are based on land use and land-use change data and bookkeeping models. Atmospheric CO2 concentration is measured directly, and its growth rate (GATM) is computed from the annual changes in concentration. The ocean CO2 sink (SOCEAN) is estimated with global ocean biogeochemistry models and observation-based data products. The terrestrial CO2 sink (SLAND) is estimated with dynamic global vegetation models. The resulting carbon budget imbalance (BIM), the difference between the estimated total emissions and the estimated changes in the atmosphere, ocean, and terrestrial biosphere, is a measure of imperfect data and understanding of the contemporary carbon cycle. All uncertainties are reported as ±1σ. For the year 2021, EFOS increased by 5.1% relative to 2020, with fossil emissions at 10.1±0.5GtCyr-1 (9.9±0.5GtCyr-1 when the cement carbonation sink is included), and ELUC was 1.1±0.7GtCyr-1, for a total anthropogenic CO2 emission (including the cement carbonation sink) of 10.9±0.8GtCyr-1 (40.0±2.9GtCO2). Also, for 2021, GATM was 5.2±0.2GtCyr-1 (2.5±0.1ppmyr-1), SOCEAN was 2.9 ±0.4GtCyr-1, and SLAND was 3.5±0.9GtCyr-1, with a BIM of -0.6GtCyr-1 (i.e. the total estimated sources were too low or sinks were too high). The global atmospheric CO2 concentration averaged over 2021 reached 414.71±0.1ppm. Preliminary data for 2022 suggest an increase in EFOS relative to 2021 of +1.0% (0.1% to 1.9%) globally and atmospheric CO2 concentration reaching 417.2ppm, more than 50% above pre-industrial levels (around 278ppm). Overall, the mean and trend in the components of the global carbon budget are consistently estimated over the period 1959-2021, but discrepancies of up to 1GtCyr-1 persist for the representation of annual to semi-decadal variability in CO2 fluxes. Comparison of estimates from multiple approaches and observations shows (1) a persistent large uncertainty in the estimate of land-use change emissions, (2) a low agreement between the different methods on the magnitude of the land CO2 flux in the northern extratropics, and (3) a discrepancy between the different methods on the strength of the ocean sink over the last decade. This living data update documents changes in the methods and data sets used in this new global carbon budget and the progress in understanding of the global carbon cycle compared with previous publications of this data set. The data presented in this work are available at 10.18160/GCP-2022 (Friedlingstein et al., 2022b).
    Repository Name: EPIC Alfred Wegener Institut
    Type: Article , peerRev
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  • 14
    Publication Date: 2023-12-19
    Description: 〈jats:p〉Abstract. Accurate assessment of anthropogenic carbon dioxide (CO2) emissions and their redistribution among the atmosphere, ocean, and terrestrial biosphere in a changing climate is critical to better understand the global carbon cycle, support the development of climate policies, and project future climate change. Here we describe and synthesize data sets and methodology to quantify the five major components of the global carbon budget and their uncertainties. Fossil CO2 emissions (EFOS) are based on energy statistics and cement production data, while emissions from land-use change (ELUC), mainly deforestation, are based on land-use and land-use change data and bookkeeping models. Atmospheric CO2 concentration is measured directly, and its growth rate (GATM) is computed from the annual changes in concentration. The ocean CO2 sink (SOCEAN) is estimated with global ocean biogeochemistry models and observation-based fCO2 products. The terrestrial CO2 sink (SLAND) is estimated with dynamic global vegetation models. Additional lines of evidence on land and ocean sinks are provided by atmospheric inversions, atmospheric oxygen measurements, and Earth system models. The resulting carbon budget imbalance (BIM), the difference between the estimated total emissions and the estimated changes in the atmosphere, ocean, and terrestrial biosphere, is a measure of imperfect data and incomplete understanding of the contemporary carbon cycle. All uncertainties are reported as ±1σ. For the year 2022, EFOS increased by 0.9 % relative to 2021, with fossil emissions at 9.9±0.5 Gt C yr−1 (10.2±0.5 Gt C yr−1 when the cement carbonation sink is not included), and ELUC was 1.2±0.7 Gt C yr−1, for a total anthropogenic CO2 emission (including the cement carbonation sink) of 11.1±0.8 Gt C yr−1 (40.7±3.2 Gt CO2 yr−1). Also, for 2022, GATM was 4.6±0.2 Gt C yr−1 (2.18±0.1 ppm yr−1; ppm denotes parts per million), SOCEAN was 2.8±0.4 Gt C yr−1, and SLAND was 3.8±0.8 Gt C yr−1, with a BIM of −0.1 Gt C yr−1 (i.e. total estimated sources marginally too low or sinks marginally too high). The global atmospheric CO2 concentration averaged over 2022 reached 417.1±0.1 ppm. Preliminary data for 2023 suggest an increase in EFOS relative to 2022 of +1.1 % (0.0 % to 2.1 %) globally and atmospheric CO2 concentration reaching 419.3 ppm, 51 % above the pre-industrial level (around 278 ppm in 1750). Overall, the mean of and trend in the components of the global carbon budget are consistently estimated over the period 1959–2022, with a near-zero overall budget imbalance, although discrepancies of up to around 1 Gt C yr−1 persist for the representation of annual to semi-decadal variability in CO2 fluxes. Comparison of estimates from multiple approaches and observations shows the following: (1) a persistent large uncertainty in the estimate of land-use changes emissions, (2) a low agreement between the different methods on the magnitude of the land CO2 flux in the northern extra-tropics, and (3) a discrepancy between the different methods on the strength of the ocean sink over the last decade. This living-data update documents changes in methods and data sets applied to this most recent global carbon budget as well as evolving community understanding of the global carbon cycle. The data presented in this work are available at https://doi.org/10.18160/GCP-2023 (Friedlingstein et al., 2023). 〈/jats:p〉
    Repository Name: EPIC Alfred Wegener Institut
    Type: Article , isiRev
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  • 15
    Electronic Resource
    Electronic Resource
    Palo Alto, Calif. : Annual Reviews
    Annual Review of Ecology, Evolution, and Systematics 28 (1997), S. 545-570 
    ISSN: 0066-4162
    Source: Annual Reviews Electronic Back Volume Collection 1932-2001ff
    Topics: Biology
    Notes: Abstract Belowground competition occurs when plants decrease the growth, survival, or fecundity of neighbors by reducing available soil resources. Competition belowground can be stronger and involve many more neighbors than aboveground competition. Physiological ecologists and population or community ecologists have traditionally studied belowground competition from different perspectives. Physiologically based studies often measure resource uptake without determining the integrated consequences for plant performance, while population or community level studies examine plant performance but fail to identify the resource intermediary or mechanism. Belowground competitive ability is correlated with such attributes as root density, surface area, and plasticity either in root growth or in the properties of enzymes involved in nutrient uptake. Unlike competition for light, in which larger plants have a disproportionate advantage by shading smaller ones, competition for soil resources is apparently more symmetric. Belowground competition often decreases with increases in nutrient levels, but it is premature to generalize about the relative importance of above- and belowground competition across resource gradients. Although shoot and root competition are often assumed to have additive effects on plant growth, some studies provide evidence to the contrary, and potential interactions between the two forms of competition should be considered in future investigations. Other research recommendations include the simultaneous study of root and shoot gaps, since their closures may not occur simultaneously, and improved estimates of the belowground neighborhood. Only by combining the tools and perspectives from physiological ecology and population and community biology can we fully understand how soil characteristics, neighborhood structure, and global climate change influence or are influenced by plant competition belowground.
    Type of Medium: Electronic Resource
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  • 16
    ISSN: 1365-2486
    Source: Blackwell Publishing Journal Backfiles 1879-2005
    Topics: Biology , Energy, Environment Protection, Nuclear Power Engineering , Geography
    Notes: This study examined root production and turnover in a California grassland during the third year of a long-term experiment with ambient (LO) and twice-ambient atmospheric CO2 (HI), using harvests, ingrowth cores, and minirhizotrons. Based on one-time harvest data, root biomass was 32% greater in the HI treatment, comparable to the stimulation of aboveground production during the study year. However, the 30–70% increase in photosynthesis under elevated CO2 for the dominant species in our system is considerably larger than the combined increase in above and belowground biomass. One possible explanation is, increased root turnover, which could be a sink for the additional fixed carbon. Cumulative root production in ingrowth cores from both treatments harvested at four dates was 2–3 times that in the single harvested cores, suggesting substantial root turnover within the growing season. Minirhizotron data confirmed this result, demonstrating that production and mortality occurred simultaneously through much of the season. As a result, cumulative root production was 54%, 47% and 44% greater than peak standing root length for the no chamber (X), LO, and HI plots, respectively. Elevated CO2, however, had little effect on rates of turnover (i.e. rates of turnover were equal in the LO and HI plots throughout most of the year) and cumulative root production was unaffected by treatment. Elevated CO2 increased monthly production of new root length (59%) only at the end of the season (April–June) when root growth had largely ceased in the LO plots but continued in the HI plots. This end-of-season increase in production coincided with an 18% greater soil moisture content in the HI plots previously described. Total standing root length was not affected by CO2 treatment. Root mortality was unaffected by elevated CO2 in all months except April, in which plants grown in the HI plots had higher mortality rates. Together, these results demonstrate that root turnover is considerable in the grassland community and easily missed by destructive soil coring. However, increased fine root turnover under elevated CO2 is apparently not a major sink for extra photosynthate in this system.
    Type of Medium: Electronic Resource
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  • 17
    ISSN: 1365-2486
    Source: Blackwell Publishing Journal Backfiles 1879-2005
    Topics: Biology , Energy, Environment Protection, Nuclear Power Engineering , Geography
    Notes: Atmospheric CO2 (Ca) has risen dramatically since preglacial times and is projected to double in the next century. As part of a 4-year study, we examined leaf gas exchange and photosynthetic acclimation in C3 and C4 plants using unique chambers that maintained a continuous Ca gradient from 200 to 550 µmol mol−1 in a natural grassland. Our goals were to characterize linear, nonlinear and threshold responses to increasing Ca from past to future Ca levels. Photosynthesis (A), stomatal conductance (gs), leaf water-use efficiency (A/gs) and leaf N content were measured in three common species: Bothriochloa ischaemum, a C4 perennial grass, Bromus japonicus, a C3 annual grass, and Solanum dimidiatum, a C3 perennial forb. Assimilation responses to internal CO2 concentrations (A/Ci curves) and photosynthetically active radiation (A/PAR curves) were also assessed, and acclimation parameters estimated from these data. Photosynthesis increased linearly with Ca in all species (P 〈 0.05). S. dimidiatum and B. ischaemum had greater carboxylation rates for Rubisco and PEP carboxylase, respectively, at subambient than superambient Ca (P 〈 0.05). To our knowledge, this is the first published evidence of A up-regulation at subambient Ca in the field. No species showed down-regulation at superambient Ca. Stomatal conductance generally showed curvilinear decreases with Ca in the perennial species (P 〈 0.05), with steeper declines over subambient Ca than superambient, suggesting that plant water relations have already changed significantly with past Ca increases. Resource-use efficiency (A/gs and A/leaf N) in all species increased linearly with Ca. As both C3 and C4 plants had significant responses in A, gs, A/gs and A/leaf N to Ca enrichment, future Ca increases in this grassland may not favour C3 species as much as originally thought. Non-linear responses and acclimation to low Ca should be incorporated into mechanistic models to better predict the effects of past and present rising Ca on grassland ecosystems.
    Type of Medium: Electronic Resource
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  • 18
    ISSN: 1365-2486
    Source: Blackwell Publishing Journal Backfiles 1879-2005
    Topics: Biology , Energy, Environment Protection, Nuclear Power Engineering , Geography
    Notes: Atmospheric CO2 concentrations are predicted to double within the next century. Despite this trend, the extent and mechanisms through which elevated CO2 affects plant diseases remain uncertain. In this study, we assessed how elevated CO2 affects a foliar fungal pathogen, Phyllosticta minima, of Acer rubrum growing in the understory at the Duke Forest free-air CO2 enrichment experiment in Durham, North Carolina. Surveys of A. rubrum saplings in the 6th, 7th, and 8th years of the CO2 exposure revealed that elevated CO2 significantly reduced disease incidence, with 22%, 27%, and 8% fewer saplings and 14%, 4%, and 5% fewer leaves infected per plant in the three consecutive years, respectively. Elevated CO2 also significantly reduced disease severity in infected plants in all years (e.g. mean lesion area reduced 35%, 50%, and 10% in 2002, 2003, and 2004, respectively). To assess the mechanisms underlying these changes, we combined leaf structural, physiological and chemical analyses with growth chamber studies of P. minima growth and host infection. In vitro exponential growth rates of P. minima were enhanced by 17% under elevated CO2, discounting the possibility that disease reductions were because of direct negative effects of elevated CO2 on fungal performance. Scanning electron micrographs (SEM) verified that conidia germ tubes of P. minima infect A. rubrum leaves by entering through the stomata. While stomatal size and density were unchanged, stomatal conductance was reduced by 21–36% under elevated CO2, providing smaller openings for infecting germ tubes. Reduced disease severity under elevated CO2 was likely due to altered leaf chemistry and reduced nutritive quality; elevated CO2 reduced leaf N by 20% and increased the C : N ratio by 20%, total phenolics by 15%, and tannins by 14% (P〈0.05 for each factor). The potential dual mechanism we describe here of reduced stomatal opening and altered leaf chemistry that results in reduced disease incidence and severity under elevated CO2 may be prevalent in many plant pathosystems where the pathogen targets the stomata.
    Type of Medium: Electronic Resource
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  • 19
    Electronic Resource
    Electronic Resource
    Oxford, UK : Blackwell Science Ltd
    Global change biology 10 (2004), S. 0 
    ISSN: 1365-2486
    Source: Blackwell Publishing Journal Backfiles 1879-2005
    Topics: Biology , Energy, Environment Protection, Nuclear Power Engineering , Geography
    Notes: Vegetation changes, particularly transitions between tree- and grass-dominated states, can alter ecosystem water balances and soluble salt fluxes. Here we outline a general predictive framework for understanding salinization of afforested grasslands based on biophysical, hydrologic, and edaphic factors. We tested this framework in 20 paired grassland and adjacent afforested plots across ten sites in the Argentine Pampas. Rapid salinization of groundwater and soils in afforested plots was associated with increased evapotranspiration and groundwater consumption by trees, with maximum salinization occurring on intermediately textured soils. Afforested plots (10–100 ha in size) showed 4–19-fold increases in groundwater salinity on silty upland soils but 〈twofold increases on clay loess soils and sand dunes. Two years of salinity and groundwater measurements at a 40 ha Eucalyptus camaldulensis plantation revealed that the plantation reduced groundwater recharge, underwent groundwater discharge on 〉50% of the days, and depressed the water table 38 cm on average compared to the adjacent grassland. Soil cores and vertical electrical soundings indicated that ≈6 kg m−2 of salts accumulated close to the water table and suggested that salinization resulted from the exclusion of fresh groundwater solutes by tree roots. Groundwater use with afforestation in the Pampas and in other regions around the world can enhance primary production and provide a tool for flood control. However, our framework and experimental data also suggest that afforestation can compromise the quality of soils and water resources in predictable ways based on water use, climate, and soil texture.
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  • 20
    Electronic Resource
    Electronic Resource
    Oxford, UK : Blackwell Science Ltd
    Global change biology 11 (2005), S. 0 
    ISSN: 1365-2486
    Source: Blackwell Publishing Journal Backfiles 1879-2005
    Topics: Biology , Energy, Environment Protection, Nuclear Power Engineering , Geography
    Notes: Carbon sequestration programs, including afforestation and reforestation, are gaining attention globally and will alter many ecosystem processes, including water yield. Some previous analyses have addressed deforestation and water yield, while the effects of afforestation on water yield have been considered for some regions. However, to our knowledge no systematic global analysis of the effects of afforestation on water yield has been undertaken. To assess and predict these effects globally, we analyzed 26 catchment data sets with 504 observations, including annual runoff and low flow. We examined changes in the context of several variables, including original vegetation type, plantation species, plantation age, and mean annual precipitation (MAP). All of these variables should be useful for understanding and modeling the effects of afforestation on water yield. We found that annual runoff was reduced on average by 44% (±3%) and 31% (±2%) when grasslands and shrublands were afforested, respectively. Eucalypts had a larger impact than other tree species in afforested grasslands (P=0.002), reducing runoff (90) by 75% (±10%), compared with a 40% (±3%) average decrease with pines. Runoff losses increased significantly with plantation age for at least 20 years after planting, whether expressed as absolute changes (mm) or as a proportion of predicted runoff (%) (P〈0.001). For grasslands, absolute reductions in annual runoff were greatest at wetter sites, but proportional reductions were significantly larger in drier sites (P〈0.01 and P〈0.001, respectively). Afforestation effects on low flow were similar to those on total annual flow, but proportional reductions were even larger for low flow (P〈0.001). These results clearly demonstrate that reductions in runoff can be expected following afforestation of grasslands and shrublands and may be most severe in drier regions. Our results suggest that, in a region where natural runoff is less than 10% of MAP, afforestation should result in a complete loss of runoff; where natural runoff is 30% of precipitation, it will likely be cut by half or more when trees are planted. The possibility that afforestation could cause or intensify water shortages in many locations is a tradeoff that should be explicitly addressed in carbon sequestration programs.
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