Inter-annual variability of the atmospheric carbon dioxide concentrations as simulated with global terrestrial biosphere models and an atmospheric transport model

Energy Technology Data Exchange (ETDEWEB)

Fujita, Daisuke; Saeki, Tazu; Nakazawa, Takakiyo [Tohoku Univ., Sendai (Japan). Center for Atmospheric and Oceanic Studies; Ishizawa, Misa; Maksyutov, Shamil [Inst. for Global Change Research, Yokohama (Japan). Frontier Research System for Global Change; Thornton, Peter E. [National Center for Atmospheric Research, Boulder, CO (United States). Climate and Global Dynamics Div.

2003-04-01

Seasonal and inter-annual variations of atmospheric CO{sub 2} for the period from 1961 to 1997 have been simulated using a global tracer transport model driven by a new version of the Biome BioGeochemical Cycle model (Biome-BGC). Biome-BGC was forced by daily temperature and precipitation from the NCEP reanalysis dataset, and the calculated monthly-averaged CO{sub 2} fluxes were used as input to the global transport model. Results from an inter-comparison with the Carnegie-Ames-Stanford Approach model (CASA) and the Simulation model of Carbon CYCLE in Land Ecosystems (Sim-CYCLE) model are also reported. The phase of the seasonal cycle in the Northern Hemisphere was reproduced generally well by Biome-BGC, although the amplitude was smaller compared to the observations and to the other biosphere models. The CO{sub 2} time series simulated by Biome-BGC were compared to the global CO{sub 2} concentration anomalies from the observations at Mauna Loa and the South Pole. The modeled concentration anomalies matched the phase of the inter-annual variations in the atmospheric CO{sub 2} observations; however, the modeled amplitude was lower than the observed value in several cases. The result suggests that a significant part of the inter-annual variability in the global carbon cycle can be accounted for by the terrestrial biosphere models. Simulations performed with another climate-based model, Sim-CYCLE, produced a larger amplitude of inter-annual variability in atmospheric CO{sub 2}, making the amplitude closer to the observed range, but with a more visible phase mismatch in a number of time periods. This may indicate the need to increase the Biome-BGC model sensitivity to seasonal and inter-annual changes in temperature and precipitation.

Inter-annual variability of the atmospheric carbon dioxide concentrations as simulated with global terrestrial biosphere models and an atmospheric transport model

International Nuclear Information System (INIS)

Fujita, Daisuke; Saeki, Tazu; Nakazawa, Takakiyo; Ishizawa, Misa; Maksyutov, Shamil; Thornton, Peter E.

2003-01-01

Seasonal and inter-annual variations of atmospheric CO 2 for the period from 1961 to 1997 have been simulated using a global tracer transport model driven by a new version of the Biome BioGeochemical Cycle model (Biome-BGC). Biome-BGC was forced by daily temperature and precipitation from the NCEP reanalysis dataset, and the calculated monthly-averaged CO 2 fluxes were used as input to the global transport model. Results from an inter-comparison with the Carnegie-Ames-Stanford Approach model (CASA) and the Simulation model of Carbon CYCLE in Land Ecosystems (Sim-CYCLE) model are also reported. The phase of the seasonal cycle in the Northern Hemisphere was reproduced generally well by Biome-BGC, although the amplitude was smaller compared to the observations and to the other biosphere models. The CO 2 time series simulated by Biome-BGC were compared to the global CO 2 concentration anomalies from the observations at Mauna Loa and the South Pole. The modeled concentration anomalies matched the phase of the inter-annual variations in the atmospheric CO 2 observations; however, the modeled amplitude was lower than the observed value in several cases. The result suggests that a significant part of the inter-annual variability in the global carbon cycle can be accounted for by the terrestrial biosphere models. Simulations performed with another climate-based model, Sim-CYCLE, produced a larger amplitude of inter-annual variability in atmospheric CO 2 , making the amplitude closer to the observed range, but with a more visible phase mismatch in a number of time periods. This may indicate the need to increase the Biome-BGC model sensitivity to seasonal and inter-annual changes in temperature and precipitation

Global Ocean Carbon and Biogeochemistry Coordination

Science.gov (United States)

Telszewski, Maciej; Tanhua, Toste; Palacz, Artur

2016-04-01

The complexity of the marine carbon cycle and its numerous connections to carbon's atmospheric and terrestrial pathways means that a wide range of approaches have to be used in order to establish it's qualitative and quantitative role in the global climate system. Ocean carbon and biogeochemistry research, observations, and modelling are conducted at national, regional, and global levels to quantify the global ocean uptake of atmospheric CO2 and to understand controls of this process, the variability of uptake and vulnerability of carbon fluxes into the ocean. These science activities require support by a sustained, international effort that provides a central communication forum and coordination services to facilitate the compatibility and comparability of results from individual efforts and development of the ocean carbon data products that can be integrated with the terrestrial, atmospheric and human dimensions components of the global carbon cycle. The International Ocean Carbon Coordination Project (IOCCP) was created in 2005 by the IOC of UNESCO and the Scientific Committee on Oceanic Research. IOCCP provides an international, program-independent forum for global coordination of ocean carbon and biogeochemistry observations and integration with global carbon cycle science programs. The IOCCP coordinates an ever-increasing set of observations-related activities in the following domains: underway observations of biogeochemical water properties, ocean interior observations, ship-based time-series observations, large-scale ocean acidification monitoring, inorganic nutrients observations, biogeochemical instruments and autonomous sensors and data and information creation. Our contribution is through the facilitation of the development of globally acceptable strategies, methodologies, practices and standards homogenizing efforts of the research community and scientific advisory groups as well as integrating the ocean biogeochemistry observations with the

Global Carbon Budget 2015

Science.gov (United States)

Le Quéré, C.; Moriarty, R.; Andrew, R. M.; Canadell, J. G.; Sitch, S.; Korsbakken, J. I.; Friedlingstein, P.; Peters, G. P.; Andres, R. J.; Boden, T. A.; Houghton, R. A.; House, J. I.; Keeling, R. F.; Tans, P.; Arneth, A.; Bakker, D. C. E.; Barbero, L.; Bopp, L.; Chang, J.; Chevallier, F.; Chini, L. P.; Ciais, P.; Fader, M.; Feely, R. A.; Gkritzalis, T.; Harris, I.; Hauck, J.; Ilyina, T.; Jain, A. K.; Kato, E.; Kitidis, V.; Klein Goldewijk, K.; Koven, C.; Landschützer, P.; Lauvset, S. K.; Lefèvre, N.; Lenton, A.; Lima, I. D.; Metzl, N.; Millero, F.; Munro, D. R.; Murata, A.; Nabel, J. E. M. S.; Nakaoka, S.; Nojiri, Y.; O'Brien, K.; Olsen, A.; Ono, T.; Pérez, F. F.; Pfeil, B.; Pierrot, D.; Poulter, B.; Rehder, G.; Rödenbeck, C.; Saito, S.; Schuster, U.; Schwinger, J.; Séférian, R.; Steinhoff, T.; Stocker, B. D.; Sutton, A. J.; Takahashi, T.; Tilbrook, B.; van der Laan-Luijkx, I. T.; van der Werf, G. R.; van Heuven, S.; Vandemark, D.; Viovy, N.; Wiltshire, A.; Zaehle, S.; Zeng, N.

2015-12-01

Accurate assessment of anthropogenic carbon dioxide (CO2) emissions and their redistribution among the atmosphere, ocean, and terrestrial biosphere 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 a methodology to quantify all major components of the global carbon budget, including their uncertainties, based on the combination of a range of data, algorithms, statistics, and model estimates and their interpretation by a broad scientific community. We discuss changes compared to previous estimates as well as consistency within and among components, alongside methodology and data limitations. CO2 emissions from fossil fuels and industry (EFF) are based on energy statistics and cement production data, while emissions from land-use change (ELUC), mainly deforestation, are based on combined evidence from land-cover-change data, fire activity associated with deforestation, and models. The global atmospheric CO2 concentration is measured directly and its rate of growth (GATM) is computed from the annual changes in concentration. The mean ocean CO2 sink (SOCEAN) is based on observations from the 1990s, while the annual anomalies and trends are estimated with ocean models. The variability in SOCEAN is evaluated with data products based on surveys of ocean CO2 measurements. The global residual terrestrial CO2 sink (SLAND) is estimated by the difference of the other terms of the global carbon budget and compared to results of independent dynamic global vegetation models forced by observed climate, CO2, and land-cover change (some including nitrogen-carbon interactions). We compare the mean land and ocean fluxes and their variability to estimates from three atmospheric inverse methods for three broad latitude bands. All uncertainties are reported as ±1σ, reflecting the current capacity to characterise the annual estimates of each component of the global

Global Carbon Budget 2016

Science.gov (United States)

Le Quéré, Corinne; Andrew, Robbie M.; Canadell, Josep G.; Sitch, Stephen; Korsbakken, Jan Ivar; Peters, Glen P.; Manning, Andrew C.; Boden, Thomas A.; Tans, Pieter P.; Houghton, Richard A.; Keeling, Ralph F.; Alin, Simone; Andrews, Oliver D.; Anthoni, Peter; Barbero, Leticia; Bopp, Laurent; Chevallier, Frédéric; Chini, Louise P.; Ciais, Philippe; Currie, Kim; Delire, Christine; Doney, Scott C.; Friedlingstein, Pierre; Gkritzalis, Thanos; Harris, Ian; Hauck, Judith; Haverd, Vanessa; Hoppema, Mario; Klein Goldewijk, Kees; Jain, Atul K.; Kato, Etsushi; Körtzinger, Arne; Landschützer, Peter; Lefèvre, Nathalie; Lenton, Andrew; Lienert, Sebastian; Lombardozzi, Danica; Melton, Joe R.; Metzl, Nicolas; Millero, Frank; Monteiro, Pedro M. S.; Munro, David R.; Nabel, Julia E. M. S.; Nakaoka, Shin-ichiro; O'Brien, Kevin; Olsen, Are; Omar, Abdirahman M.; Ono, Tsuneo; Pierrot, Denis; Poulter, Benjamin; Rödenbeck, Christian; Salisbury, Joe; Schuster, Ute; Schwinger, Jörg; Séférian, Roland; Skjelvan, Ingunn; Stocker, Benjamin D.; Sutton, Adrienne J.; Takahashi, Taro; Tian, Hanqin; Tilbrook, Bronte; van der Laan-Luijkx, Ingrid T.; van der Werf, Guido R.; Viovy, Nicolas; Walker, Anthony P.; Wiltshire, Andrew J.; Zaehle, Sönke

2016-11-01

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 all major components of the global carbon budget, including their uncertainties, based on the combination of a range of data, algorithms, statistics, and model estimates and their interpretation by a broad scientific community. We discuss changes compared to previous estimates and consistency within and among components, alongside methodology and data limitations. 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 combined evidence from land-cover change data, fire activity associated with deforestation, and models. The global atmospheric CO2 concentration is measured directly and its rate of growth (GATM) is computed from the annual changes in concentration. The mean ocean CO2 sink (SOCEAN) is based on observations from the 1990s, while the annual anomalies and trends are estimated with ocean models. The variability in SOCEAN is evaluated with data products based on surveys of ocean CO2 measurements. The global residual terrestrial CO2 sink (SLAND) is estimated by the difference of the other terms of the global carbon budget and compared to results of independent dynamic global vegetation models. We compare the mean land and ocean fluxes and their variability to estimates from three atmospheric inverse methods for three broad latitude bands. All uncertainties are reported as ±1σ, reflecting the current capacity to characterise the annual estimates of each component of the global carbon budget. For the last decade available (2006-2015), EFF was 9

Regional pattern and interannual variations in global terrestrial carbon uptake in response to changes in climate and atmospheric CO2

International Nuclear Information System (INIS)

Cao, Mingkui; Tao, B.; Li, Kerang; Prince, Stephen D.; Small, J.

2005-01-01

Atmospheric measurements indicate that the terrestrial carbon sink increased substantially from the 1980s to the 1990s, but which factors and regions were responsible for the increase are not well identified yet. Using process- and remote sensing-based ecosystem models, we show that changes in climate and atmospheric CO 2 in the period 1981-2000 enhanced net ecosystem production (NEP) and caused major geographical changes in the global distribution of NEP. In the 1980s the Americas accounted for almost all of the global NEP, but in the 1990s NEP in Eurasia and Africa became higher than that of the Americas. The year-to-year variation in global NEP was up to 2.5 Pg C (1 Pg = 10 15 g), in which 1.4 Pg C was attributable to the El Nino Southern Oscillation cycle (ENSO). NEP clearly decreased in El Nino and increased in La Nina in South America and Africa, but the response in North America and Eurasia was mixed. The estimated NEP increases accounted for only 30% of the global terrestrial carbon sink but can explain almost all of the increase from the 1980s to the 1990s. Because a large part of the increase in NEP was driven by the long-term trend of climate and atmospheric CO 2 , the increase in the global terrestrial carbon sink from the 1980s to the 1990s was a continuation of the trend since the middle of the twentieth century, rather than merely a consequence of short-time climate variability

Global Carbon Budget 2017

Directory of Open Access Journals (Sweden)

C. Le Quéré

2018-03-01

Full Text Available 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

Ecosystem-atmosphere exchange of carbon in a heathland under future climatic conditions

Energy Technology Data Exchange (ETDEWEB)

Bang Selsted, M

2010-07-15

Global change is a reality. Atmospheric CO{sub 2} levels are rising as well as mean global temperature and precipitation patterns are changing. These three environmental factors have separately and in combination effect on ecosystem processes. Terrestrial ecosystems hold large amounts of carbon, why understanding plant and soil responses to such changes are necessary, as ecosystems potentially can ameliorate or accelerate global change. To predict the feedback of ecosystems to the atmospheric CO{sub 2} concentrations experiments imitating global change effects are therefore an important tool. This work on ecosystem-atmosphere exchange of carbon in a heathland under future climatic conditions, shows that extended summer drought in combination with elevated temperature will ensure permanent dryer soil conditions, which decreases carbon turnover, while elevated atmospheric CO{sub 2} concentrations will increase carbon turnover. In the full future climate scenario, carbon turnover is over all expected to increase and the heathland to become a source of atmospheric CO{sub 2}. The methodology of static chamber CO{sub 2} flux measurements and applying the technology in a FACE (free air CO{sub 2} enrichment) facility is a challenge. Fluxes of CO{sub 2} from soil to atmosphere depend on a physical equilibrium between those two medias, why it is important to keep the CO{sub 2} gradient between soil and atmosphere unchanged during measurement. Uptake to plants via photosynthesis depends on a physiological process, which depends strongly on the atmospheric CO{sub 2} concentration. Photosynthesis and respiration run in parallel during measurements of net ecosystem exchange, and these measurements should therefore be performed with care to both the atmospheric CO{sub 2} concentration and the CO{sub 2} soil-atmosphere gradient. (author)

The ocean quasi-homogeneous layer model and global cycle of carbon dioxide in system of atmosphere-ocean

Science.gov (United States)

Glushkov, Alexander; Glushkov, Alexander; Loboda, Nataliya; Khokhlov, Valery; Serbov, Nikoly; Svinarenko, Andrey

The purpose of this paper is carrying out the detailed model of the CO2 global turnover in system of "atmosphere-ocean" with using the ocean quasi-homogeneous layer model. Practically all carried out models are functioning in the average annual regime and accounting for the carbon distribution in bio-sphere in most general form (Glushkov et al, 2003). We construct a modified model for cycle of the carbon dioxide, which allows to reproduce a season dynamics of carbon turnover in ocean with account of zone ocean structure (up quasi-homogeneous layer, thermocline and deepest layer). It is taken into account dependence of the CO2 transfer through the bounder between atmosphere and ocean upon temperature of water and air, wind velocity, buffer mechanism of the CO2 dissolution. The same program is realized for atmosphere part of whole system. It is obtained a tempo-ral and space distribution for concentration of non-organic carbon in ocean, partial press of dissolute CO2 and value of exchange on the border between atmosphere and ocean. It is estimated a role of the wind intermixing of the up ocean layer. The increasing of this effect leads to increasing the plankton mass and further particles, which are transferred by wind, contribute to more quick immersion of microscopic shells and organic material. It is fulfilled investigation of sen-sibility of the master differential equations system solutions from the model parameters. The master differential equa-tions system, describing a dynamics of the CO2 cycle, is numerically integrated by the four order Runge-Cutt method under given initial values of valuables till output of solution on periodic regime. At first it is indicated on possible real-zation of the chaos scenario in system. On our data, the difference of the average annual values for the non-organic car-bon concentration in the up quasi-homogeneous layer between equator and extreme southern zone is 0.15 mol/m3, be-tween the equator and extreme northern zone is 0

Global carbon budget 2013

International Nuclear Information System (INIS)

Le Quere, C.; Moriarty, R.; Jones, S.D.; Boden, T.A.; Peters, G.P.; Andrew, R.M.; Andres, R.J.; Ciais, P.; Bopp, L.; Maignan, F.; Viovy, N.

2014-01-01

Accurate assessment of anthropogenic carbon dioxide (CO 2 ) emissions and their redistribution among the atmosphere, ocean, and terrestrial biosphere 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 a methodology to quantify all major components of the global carbon budget, including their uncertainties, based on the combination of a range of data, algorithms, statistics and model estimates and their interpretation by a broad scientific community. We discuss changes compared to previous estimates, consistency within and among components, alongside methodology and data limitations. CO 2 emissions from fossil-fuel combustion and cement production (EFF) are based on energy statistics, while emissions from land-use change (ELUC), mainly deforestation, are based on combined evidence from land-cover change data, fire activity associated with deforestation, and models. The global atmospheric CO 2 concentration is measured directly and its rate of growth (GATM) is computed from the annual changes in concentration. The mean ocean CO 2 sink (SOCEAN) is based on observations from the 1990's, while the annual anomalies and trends are estimated with ocean models. The variability in SOCEAN is evaluated for the first time in this budget with data products based on surveys of ocean CO 2 measurements. The global residual terrestrial CO 2 sink (SLAND) is estimated by the difference of the other terms of the global carbon budget and compared to results of independent dynamic global vegetation models forced by observed climate, CO 2 and land cover change (some including nitrogen-carbon interactions). All uncertainties are reported as ±1, reflecting the current capacity to characterise the annual estimates of each component of the global carbon budget. For the last decade available (2003-2012), EFF was 8.6±0.4 GtC yr -1 , ELUC 0.9±0.5 GtC yr -1 , GATM 4.3±0

Modeling seasonal changes of atmospheric carbon dioxide and carbon 13

International Nuclear Information System (INIS)

Gillette, D.A.; Box, E.O.

1986-01-01

A two-dimensional (latitude-altitude) model of atmospheric CO 2 and δ 13 C was constructed to simulate some features of seasonal carbon cycle fluctuations. The model simulates air-sea exchange, atmospheric diffusion, and fossil fuel carbon sources, which are functions of time and latitude. In addition, it uses biosphere-atmosphere fluxes of carbon that are based on global-scale biological models of vegetation growth and decay. Results of the model show fair agreement with observational results for CO 2 and δ 13 C seasonal fluctuations. Their model results have far northern fluctuations with smaller amplitudes than are observed. Analysis of sources of CO 2 change at given latitudes shows that, for far southern latitudes, southern hemisphere biospheric fluxes are dominant in affecting the seasonal CO 2 fluctuations. Long-term decrease of δ 13 C for the model is larger than for observations. This may be due to errors in the formulation for oceanic fluxes for 13 C in the model or to a net uptake of carbon by the biosphere

Environmental effects of increased atmospheric carbon dioxide

International Nuclear Information System (INIS)

Soon, W.; Baliunas, S.L.; Robinson, A.B.; Robinson, Z.W.

1999-01-01

A review of the literature concerning the environmental consequences of increased levels of atmospheric carbon dioxide leads to the conclusion that increases during the 20th century have produced no deleterious effects upon global climate or temperature. Increased carbon dioxide has, however, markedly increased plant growth rates as inferred from numerous laboratory and field experiments. There is no clear evidence, nor unique attribution, of the global effects of anthropogenic CO 2 on climate. Meaningful integrated assessments of the environmental impacts of anthropogenic CO 2 are not yet possible because model estimates of global and regional climate changes on interannual, decadal and centennial timescales remain highly uncertain.(author)

Optimization of Terrestrial Ecosystem Model Parameters Using Atmospheric CO2 Concentration Data With the Global Carbon Assimilation System (GCAS)

Science.gov (United States)

Chen, Zhuoqi; Chen, Jing M.; Zhang, Shupeng; Zheng, Xiaogu; Ju, Weiming; Mo, Gang; Lu, Xiaoliang

2017-12-01

The Global Carbon Assimilation System that assimilates ground-based atmospheric CO2 data is used to estimate several key parameters in a terrestrial ecosystem model for the purpose of improving carbon cycle simulation. The optimized parameters are the leaf maximum carboxylation rate at 25°C (Vmax25), the temperature sensitivity of ecosystem respiration (Q10), and the soil carbon pool size. The optimization is performed at the global scale at 1° resolution for the period from 2002 to 2008. The results indicate that vegetation from tropical zones has lower Vmax25 values than vegetation in temperate regions. Relatively high values of Q10 are derived over high/midlatitude regions. Both Vmax25 and Q10 exhibit pronounced seasonal variations at middle-high latitudes. The maxima in Vmax25 occur during growing seasons, while the minima appear during nongrowing seasons. Q10 values decrease with increasing temperature. The seasonal variabilities of Vmax25 and Q10 are larger at higher latitudes. Optimized Vmax25 and Q10 show little seasonal variabilities at tropical regions. The seasonal variabilities of Vmax25 are consistent with the variabilities of LAI for evergreen conifers and broadleaf evergreen forests. Variations in leaf nitrogen and leaf chlorophyll contents may partly explain the variations in Vmax25. The spatial distribution of the total soil carbon pool size after optimization is compared favorably with the gridded Global Soil Data Set for Earth System. The results also suggest that atmospheric CO2 data are a source of information that can be tapped to gain spatially and temporally meaningful information for key ecosystem parameters that are representative at the regional and global scales.

Formulating Energy Policies Related to Fossil Fuel Use: Critical Uncertainties in the Global Carbon Cycle

Science.gov (United States)

Post, W. M.; Dale, V. H.; DeAngelis, D. L.; Mann, L. K.; Mulholland, P. J.; O`Neill, R. V.; Peng, T. -H.; Farrell, M. P.

1990-02-01

The global carbon cycle is the dynamic interaction among the earth's carbon sources and sinks. Four reservoirs can be identified, including the atmosphere, terrestrial biosphere, oceans, and sediments. Atmospheric CO{sub 2} concentration is determined by characteristics of carbon fluxes among major reservoirs of the global carbon cycle. The objective of this paper is to document the knowns, and unknowns and uncertainties associated with key questions that if answered will increase the understanding of the portion of past, present, and future atmospheric CO{sub 2} attributable to fossil fuel burning. Documented atmospheric increases in CO{sub 2} levels are thought to result primarily from fossil fuel use and, perhaps, deforestation. However, the observed atmospheric CO{sub 2} increase is less than expected from current understanding of the global carbon cycle because of poorly understood interactions among the major carbon reservoirs.

Constraining the global carbon budget from global to regional scales - The measurement challenge

International Nuclear Information System (INIS)

Francey, R.J.; Rayner, P.J.; Allison, C.E.

2002-01-01

The Global Carbon Cycle can be modelled by a Bayesian synthesis inversion technique, where measured atmospheric CO 2 concentrations and isotopic compositions are analysed by use of an atmospheric transport model and estimates of regional sources and sinks of atmospheric carbon. The uncertainty associated to carbon flux estimates even on a regional scale can be improved considerably using the inversion technique. In this approach, besides the necessary control on the precision of atmospheric transport models and on the constraints for surface fluxes, an important component is the calibration of atmospheric CO 2 concentration and isotope measurements. The recent improved situation in respect to data comparability is discussed using results of conducted interlaboratory comparison exercises and larger scale calibration programs are proposed for the future to further improve the comparability of analytical data. (author)

Assessing Students' Disciplinary and Interdisciplinary Understanding of Global Carbon Cycling

Science.gov (United States)

You, Hye Sun; Marshall, Jill A.; Delgado, Cesar

2018-01-01

Global carbon cycling describes the movement of carbon through atmosphere, biosphere, geosphere, and hydrosphere; it lies at the heart of climate change and sustainability. To understand the global carbon cycle, students will require "interdisciplinary knowledge." While standards documents in science education have long promoted…

The global pyrogenic carbon cycle and its impact on the level of atmospheric CO2 over past and future centuries.

Science.gov (United States)

Landry, Jean-Sébastien; Matthews, H Damon

2017-08-01

The incomplete combustion of vegetation and dead organic matter by landscape fires creates recalcitrant pyrogenic carbon (PyC), which could be consequential for the global carbon budget if changes in fire regime, climate, and atmospheric CO 2 were to substantially affect gains and losses of PyC on land and in oceans. Here, we included global PyC cycling in a coupled climate-carbon model to assess the role of PyC in historical and future simulations, accounting for uncertainties through five sets of parameter estimates. We obtained year-2000 global stocks of (Central estimate, likely uncertainty range in parentheses) 86 (11-154), 47 (2-64), and 1129 (90-5892) Pg C for terrestrial residual PyC (RPyC), marine dissolved PyC, and marine particulate PyC, respectively. PyC cycling decreased atmospheric CO 2 only slightly between 1751 and 2000 (by 0.8 Pg C for the Central estimate) as PyC-related fluxes changed little over the period. For 2000 to 2300, we combined Representative Concentration Pathways (RCPs) 4.5 and 8.5 with stable or continuously increasing future fire frequencies. For the increasing future fire regime, the production of new RPyC generally outpaced the warming-induced accelerated loss of existing RPyC, so that PyC cycling decreased atmospheric CO 2 between 2000 and 2300 for most estimates (by 4-8 Pg C for Central). For the stable fire regime, however, PyC cycling usually increased atmospheric CO 2 (by 1-9 Pg C for Central), and only the most extreme choice of parameters maximizing PyC production and minimizing PyC decomposition led to atmospheric CO 2 decreases under RCPs 4.5 and 8.5 (by 5-8 Pg C). Our results suggest that PyC cycling will likely reduce the future increase in atmospheric CO 2 if landscape fires become much more frequent; however, in the absence of a substantial increase in fire frequency, PyC cycling might contribute to, rather than mitigate, the future increase in atmospheric CO 2 . © 2016 John Wiley & Sons Ltd.

Old-growth forests as global carbon sinks

NARCIS (Netherlands)

Luyssaert, S; Schulze, E.D.; Börner, A.

2008-01-01

Old- growth forests remove carbon dioxide from the atmosphere(1,2) at rates that vary with climate and nitrogen deposition(3). The sequestered carbon dioxide is stored in live woody tissues and slowly decomposing organic matter in litter and soil(4). Old- growth forests therefore serve as a global

Reviews and syntheses: An empirical spatiotemporal description of the global surface–atmosphere carbon fluxes: opportunities and data limitations

Directory of Open Access Journals (Sweden)

J. Zscheischler

2017-08-01

Full Text Available Understanding the global carbon (C cycle is of crucial importance to map current and future climate dynamics relative to global environmental change. A full characterization of C cycling requires detailed information on spatiotemporal patterns of surface–atmosphere fluxes. However, relevant C cycle observations are highly variable in their coverage and reporting standards. Especially problematic is the lack of integration of the carbon dioxide (CO2 exchange of the ocean, inland freshwaters and the land surface with the atmosphere. Here we adopt a data-driven approach to synthesize a wide range of observation-based spatially explicit surface–atmosphere CO2 fluxes from 2001 to 2010, to identify the state of today's observational opportunities and data limitations. The considered fluxes include net exchange of open oceans, continental shelves, estuaries, rivers, and lakes, as well as CO2 fluxes related to net ecosystem productivity, fire emissions, loss of tropical aboveground C, harvested wood and crops, as well as fossil fuel and cement emissions. Spatially explicit CO2 fluxes are obtained through geostatistical and/or remote-sensing-based upscaling, thereby minimizing biophysical or biogeochemical assumptions encoded in process-based models. We estimate a bottom-up net C exchange (NCE between the surface (land, ocean, and coastal areas and the atmosphere. Though we provide also global estimates, the primary goal of this study is to identify key uncertainties and observational shortcomings that need to be prioritized in the expansion of in situ observatories. Uncertainties for NCE and its components are derived using resampling. In many regions, our NCE estimates agree well with independent estimates from other sources such as process-based models and atmospheric inversions. This holds for Europe (mean ± 1 SD: 0.8 ± 0.1 PgC yr−1, positive numbers are sources to the atmosphere, Russia (0.1 ± 0.4 PgC yr−1, East Asia

Reviews and syntheses: An empirical spatiotemporal description of the global surface-atmosphere carbon fluxes: opportunities and data limitations

Science.gov (United States)

Zscheischler, Jakob; Mahecha, Miguel D.; Avitabile, Valerio; Calle, Leonardo; Carvalhais, Nuno; Ciais, Philippe; Gans, Fabian; Gruber, Nicolas; Hartmann, Jens; Herold, Martin; Ichii, Kazuhito; Jung, Martin; Landschützer, Peter; Laruelle, Goulven G.; Lauerwald, Ronny; Papale, Dario; Peylin, Philippe; Poulter, Benjamin; Ray, Deepak; Regnier, Pierre; Rödenbeck, Christian; Roman-Cuesta, Rosa M.; Schwalm, Christopher; Tramontana, Gianluca; Tyukavina, Alexandra; Valentini, Riccardo; van der Werf, Guido; West, Tristram O.; Wolf, Julie E.; Reichstein, Markus

2017-08-01

Understanding the global carbon (C) cycle is of crucial importance to map current and future climate dynamics relative to global environmental change. A full characterization of C cycling requires detailed information on spatiotemporal patterns of surface-atmosphere fluxes. However, relevant C cycle observations are highly variable in their coverage and reporting standards. Especially problematic is the lack of integration of the carbon dioxide (CO2) exchange of the ocean, inland freshwaters and the land surface with the atmosphere. Here we adopt a data-driven approach to synthesize a wide range of observation-based spatially explicit surface-atmosphere CO2 fluxes from 2001 to 2010, to identify the state of today's observational opportunities and data limitations. The considered fluxes include net exchange of open oceans, continental shelves, estuaries, rivers, and lakes, as well as CO2 fluxes related to net ecosystem productivity, fire emissions, loss of tropical aboveground C, harvested wood and crops, as well as fossil fuel and cement emissions. Spatially explicit CO2 fluxes are obtained through geostatistical and/or remote-sensing-based upscaling, thereby minimizing biophysical or biogeochemical assumptions encoded in process-based models. We estimate a bottom-up net C exchange (NCE) between the surface (land, ocean, and coastal areas) and the atmosphere. Though we provide also global estimates, the primary goal of this study is to identify key uncertainties and observational shortcomings that need to be prioritized in the expansion of in situ observatories. Uncertainties for NCE and its components are derived using resampling. In many regions, our NCE estimates agree well with independent estimates from other sources such as process-based models and atmospheric inversions. This holds for Europe (mean ± 1 SD: 0.8 ± 0.1 PgC yr-1, positive numbers are sources to the atmosphere), Russia (0.1 ± 0.4 PgC yr-1), East Asia (1.6 ± 0.3 PgC yr-1), South Asia (0.3 ± 0

Africa and the global carbon cycle

Directory of Open Access Journals (Sweden)

Denning A Scott

2007-03-01

Full Text Available Abstract The African continent has a large and growing role in the global carbon cycle, with potentially important climate change implications. However, the sparse observation network in and around the African continent means that Africa is one of the weakest links in our understanding of the global carbon cycle. Here, we combine data from regional and global inventories as well as forward and inverse model analyses to appraise what is known about Africa's continental-scale carbon dynamics. With low fossil emissions and productivity that largely compensates respiration, land conversion is Africa's primary net carbon release, much of it through burning of forests. Savanna fire emissions, though large, represent a short-term source that is offset by ensuing regrowth. While current data suggest a near zero decadal-scale carbon balance, interannual climate fluctuations (especially drought induce sizeable variability in net ecosystem productivity and savanna fire emissions such that Africa is a major source of interannual variability in global atmospheric CO2. Considering the continent's sizeable carbon stocks, their seemingly high vulnerability to anticipated climate and land use change, as well as growing populations and industrialization, Africa's carbon emissions and their interannual variability are likely to undergo substantial increases through the 21st century.

Global carbon cycle and possible disturbances due to man's interventions

Energy Technology Data Exchange (ETDEWEB)

Pankrath, J

1979-01-01

Global atmospheric CO/sub 2/ concentration has increased since the beginning of reliable monitoring in 1958 at a mean rate of about 0.9 ppM CO/sub 2//y. Now, atmospheric, CO/sub 2/ concentration is at 330 ppM. From about 1860 up to 1974, man's intervention in the global carbon cycle caused a likely increase of 76.6 x 10/sup 15/ g C, corresponding to 36 ppM CO/sub 2/ in the atmosphere, if a preindustrial content of 294 ppM CO/sub 2/ or 625.3 x 10/sup 15/ g C is adopted to be valid. A further rise of atmospheric CO/sub 2/ seems to be inevitable and probably will be responsible for a climatic warming in the next several decades; therefore, a global examination of carbon reservoirs and carbon fluxes has been undertaken to determine their storage capacity for excess carbon which originated mainly from burning of fossil fuels and from land clearing. During 1860 to 1974 about 136 x 10/sup 15/ g C have been emitted into the atmosphere by fossil fuel combustion and cement production. At present, the emission rate is about 5 x 10/sup 15/ g C/y. The worldwide examination of carbon release, primarily by deforestation and soil cultivation since 1860, is estimated to be about 120 x 10/sup 15/ g C. The net transfer of carbon to the atmosphere owing to man's interference with the biosphere is now believed to be about 2.4 x 10/sup 15/ g C/y. An oceanic uptake of rougly 179 x 10/sup 15/ g C since 1860 is open to discussion. According to the chemical buffering of sea surface water only about 35.5 x 10/sup 15/ g C could have been absorbed. It is argued, however, that oceanic circulations might have been more effective in removing atmospheric excess carbon of anthropogenic origin.

Estimation of the global climate effect of brown carbon

Science.gov (United States)

Zhang, A.; Wang, Y.; Zhang, Y.; Weber, R. J.; Song, Y.

2017-12-01

Carbonaceous aerosols significantly affect global radiative forcing and climate through absorption and scattering of sunlight. Black carbon (BC) and brown carbon (BrC) are light-absorbing carbonaceous aerosols. The global distribution and climate effect of BrC is uncertain. A recent study suggests that BrC absorption is comparable to BC in the upper troposphere over biomass burning region and that the resulting heating tends to stabilize the atmosphere. Yet current climate models do not include proper treatments of BrC. In this study, we derived a BrC global biomass burning emission inventory from Global Fire Emissions Database 4 (GFED4) and developed a BrC module in the Community Atmosphere Model version 5 (CAM5) of Community Earth System Model (CESM) model. The model simulations compared well to BrC observations of the Studies of Emissions, Atmospheric Composition, Clouds and Climate Coupling by Regional Surveys (SEAC4RS) and Deep Convective Clouds and Chemistry Project (DC-3) campaigns and includes BrC bleaching. Model results suggested that BrC in the upper troposphere due to convective transport is as important an absorber as BC globally. Upper tropospheric BrC radiative forcing is particularly significant over the tropics, affecting the atmosphere stability and Hadley circulation.

Collision and radiative processes in emission of atmospheric carbon dioxide

Science.gov (United States)

Smirnov, B. M.

2018-05-01

The peculiarities of the spectroscopic properties of CO2 molecules in air due to vibration-rotation radiative transitions are analyzed. The absorption coefficient due to atmospheric carbon dioxide and other atmospheric components is constructed within the framework of the standard atmosphere model, on the basis of classical molecular spectroscopy and the regular model for the spectroscopy absorption band. The radiative flux from the atmosphere toward the Earth is represented as that of a blackbody, and the radiative temperature for emission at a given frequency is determined with accounting for the local thermodynamic equilibrium, a small gradient of the tropospheric temperature and a high optical thickness of the troposphere for infrared radiation. The absorption band model with an absorption coefficient averaged over the frequency and line-by-line model are used for evaluating the radiative flux from the atmosphere to the Earth which values are nearby for these models and are equal W m‑2 for the contemporary concentration of atmospheric CO2 molecules and W m‑2 at its doubled value. The absorption band model is not suitable to calculate the radiative flux change at doubling of carbon dioxide concentration because averaging over oscillations decreases the range where the atmospheric optical thickness is of the order of one, and just this range determines this change. The line-by-line method gives the change of the global temperature K as a result of doubling the carbon dioxide concentration. The contribution to the global temperature change due to anthropogenic injection of carbon dioxide in the atmosphere, i.e. resulted from combustion of fossil fuels, is approximately 0.02 K now.

Enhanced priming of old, not new soil carbon at elevated atmospheric CO2

DEFF Research Database (Denmark)

Vestergard, Mette; Reinsch, Sabine; Bengtson, Per

2016-01-01

Rising atmospheric CO2 concentrations accompanied by global warming and altered precipitation patterns calls for assessment of long-term effects of these global changes on carbon (C) dynamics in terrestrial ecosystems, as changes in net C exchange between soil and atmosphere will impact the atmos......Rising atmospheric CO2 concentrations accompanied by global warming and altered precipitation patterns calls for assessment of long-term effects of these global changes on carbon (C) dynamics in terrestrial ecosystems, as changes in net C exchange between soil and atmosphere will impact...... accelerate the decomposition of soil organic C (SOC), a phenomenon termed ‘the priming effect’, and the priming effect is most pronounced at low soil N availability. Hence, we hypothesized that priming of SOC decomposition in response to labile C addition would increase in soil exposed to long-term elevated...... decomposition of relatively old SOC fractions, i.e. SOC assimilated more than 8 years before sampling....

A joint global carbon inversion system using both CO2 and 13CO2 atmospheric concentration data

Science.gov (United States)

Chen, Jing M.; Mo, Gang; Deng, Feng

2017-03-01

Observations of 13CO2 at 73 sites compiled in the GLOBALVIEW database are used for an additional constraint in a global atmospheric inversion of the surface CO2 flux using CO2 observations at 210 sites (62 collocated with 13CO2 sites) for the 2002-2004 period for 39 land regions and 11 ocean regions. This constraint is implemented using prior CO2 fluxes estimated with a terrestrial ecosystem model and an ocean model. These models simulate 13CO2 discrimination rates of terrestrial photosynthesis and ocean-atmosphere diffusion processes. In both models, the 13CO2 disequilibrium between fluxes to and from the atmosphere is considered due to the historical change in atmospheric 13CO2 concentration. This joint inversion system using both13CO2 and CO2 observations is effectively a double deconvolution system with consideration of the spatial variations of isotopic discrimination and disequilibrium. Compared to the CO2-only inversion, this 13CO2 constraint on the inversion considerably reduces the total land carbon sink from 3.40 ± 0.84 to 2.53 ± 0.93 Pg C year-1 but increases the total oceanic carbon sink from 1.48 ± 0.40 to 2.36 ± 0.49 Pg C year-1. This constraint also changes the spatial distribution of the carbon sink. The largest sink increase occurs in the Amazon, while the largest source increases are in southern Africa, and Asia, where CO2 data are sparse. Through a case study, in which the spatial distribution of the annual 13CO2 discrimination rate over land is ignored by treating it as a constant at the global average of -14. 1 ‰, the spatial distribution of the inverted CO2 flux over land was found to be significantly modified (up to 15 % for some regions). The uncertainties in our disequilibrium flux estimation are 8.0 and 12.7 Pg C year-1 ‰ for land and ocean, respectively. These uncertainties induced the unpredictability of 0.47 and 0.54 Pg C year-1 in the inverted CO2 fluxes for land and ocean, respectively. Our joint inversion system is therefore

Quantifying global soil carbon losses in response to warming.

Science.gov (United States)

Crowther, T W; Todd-Brown, K E O; Rowe, C W; Wieder, W R; Carey, J C; Machmuller, M B; Snoek, B L; Fang, S; Zhou, G; Allison, S D; Blair, J M; Bridgham, S D; Burton, A J; Carrillo, Y; Reich, P B; Clark, J S; Classen, A T; Dijkstra, F A; Elberling, B; Emmett, B A; Estiarte, M; Frey, S D; Guo, J; Harte, J; Jiang, L; Johnson, B R; Kröel-Dulay, G; Larsen, K S; Laudon, H; Lavallee, J M; Luo, Y; Lupascu, M; Ma, L N; Marhan, S; Michelsen, A; Mohan, J; Niu, S; Pendall, E; Peñuelas, J; Pfeifer-Meister, L; Poll, C; Reinsch, S; Reynolds, L L; Schmidt, I K; Sistla, S; Sokol, N W; Templer, P H; Treseder, K K; Welker, J M; Bradford, M A

2016-11-30

The majority of the Earth's terrestrial carbon is stored in the soil. If anthropogenic warming stimulates the loss of this carbon to the atmosphere, it could drive further planetary warming. Despite evidence that warming enhances carbon fluxes to and from the soil, the net global balance between these responses remains uncertain. Here we present a comprehensive analysis of warming-induced changes in soil carbon stocks by assembling data from 49 field experiments located across North America, Europe and Asia. We find that the effects of warming are contingent on the size of the initial soil carbon stock, with considerable losses occurring in high-latitude areas. By extrapolating this empirical relationship to the global scale, we provide estimates of soil carbon sensitivity to warming that may help to constrain Earth system model projections. Our empirical relationship suggests that global soil carbon stocks in the upper soil horizons will fall by 30 ± 30 petagrams of carbon to 203 ± 161 petagrams of carbon under one degree of warming, depending on the rate at which the effects of warming are realized. Under the conservative assumption that the response of soil carbon to warming occurs within a year, a business-as-usual climate scenario would drive the loss of 55 ± 50 petagrams of carbon from the upper soil horizons by 2050. This value is around 12-17 per cent of the expected anthropogenic emissions over this period. Despite the considerable uncertainty in our estimates, the direction of the global soil carbon response is consistent across all scenarios. This provides strong empirical support for the idea that rising temperatures will stimulate the net loss of soil carbon to the atmosphere, driving a positive land carbon-climate feedback that could accelerate climate change.

Isotope aided studies of atmospheric carbon dioxide and other greenhouse gases. Phase II

Energy Technology Data Exchange (ETDEWEB)

NONE

2002-01-01

The substantial increase in atmospheric greenhouse gas concentrations and their role in global warming have become major concerns of world governments. Application of isotope techniques to label sources and sinks of CO{sub 2} and other greenhouse gases has emerged as a potentially powerful method for reducing uncertainties in the global CO{sub 2} budgets and for tracing pathways and interaction of terrestrial, oceanic, and atmospheric pools of carbon. As with CO{sub 2} concentration measurements, meaningful integration of isotopes in global models requires careful attention to quality assurance, quality control and inter-comparability of measurements made by a number of networks and laboratories. To support improvements in isotope measurement capabilities, the IAEA began implementing Co-ordinated Research Projects (CRPs) in 1992. The first project, entitled Isotope Variations of Carbon Dioxide and other Trace Gases in the Atmosphere, was implemented from 1992 to 1994. A significant contribution was made towards a better understanding of the global carbon cycle and especially of the sources and sinks of carbon with data on the {sup 14}C and {sup 13}C content of atmospheric CO{sub 2}, pointing to a better understanding of the problem of the 'missing sink' in the global carbon cycle. Important methodological developments in the field of high precision stable isotope mass spectrometry and improved data acquisition procedures emerged from work carried out within the framework of this programme. The development of pressurized gas standards and planning for an associated interlaboratory calibration were initiated. Due to the good progress and long standing nature of the required work a second CRP was initiated and implemented from 1996 to 1999. It was entitled Isotope aided Studies of Atmospheric Carbon Dioxide and Other Trace Gases - Phase II, to document the close relationship of both programmes. This publication provides an overview of the scientific outcomes of the

Isotope aided studies of atmospheric carbon dioxide and other greenhouse gases. Phase II

International Nuclear Information System (INIS)

2002-01-01

The substantial increase in atmospheric greenhouse gas concentrations and their role in global warming have become major concerns of world governments. Application of isotope techniques to label sources and sinks of CO 2 and other greenhouse gases has emerged as a potentially powerful method for reducing uncertainties in the global CO 2 budgets and for tracing pathways and interaction of terrestrial, oceanic, and atmospheric pools of carbon. As with CO 2 concentration measurements, meaningful integration of isotopes in global models requires careful attention to quality assurance, quality control and inter-comparability of measurements made by a number of networks and laboratories. To support improvements in isotope measurement capabilities, the IAEA began implementing Co-ordinated Research Projects (CRPs) in 1992. The first project, entitled Isotope Variations of Carbon Dioxide and other Trace Gases in the Atmosphere, was implemented from 1992 to 1994. A significant contribution was made towards a better understanding of the global carbon cycle and especially of the sources and sinks of carbon with data on the 14 C and 13 C content of atmospheric CO 2 , pointing to a better understanding of the problem of the 'missing sink' in the global carbon cycle. Important methodological developments in the field of high precision stable isotope mass spectrometry and improved data acquisition procedures emerged from work carried out within the framework of this programme. The development of pressurized gas standards and planning for an associated interlaboratory calibration were initiated. Due to the good progress and long standing nature of the required work a second CRP was initiated and implemented from 1996 to 1999. It was entitled Isotope aided Studies of Atmospheric Carbon Dioxide and Other Trace Gases - Phase II, to document the close relationship of both programmes. This publication provides an overview of the scientific outcomes of the studies conducted within Phase

Carbon Dioxide and Global Warming: A Failed Experiment

Science.gov (United States)

Ribeiro, Carla

2014-01-01

Global warming is a current environmental issue that has been linked to an increase in anthropogenic carbon dioxide in the atmosphere. To raise awareness of the problem, various simple experiments have been proposed to demonstrate the effect of carbon dioxide on the planet's temperature. This article describes a similar experiment, which…

Vulnerability of permafrost carbon to climate change: implications for the global carbon cycle

Science.gov (United States)

Edward A.G. Schuur; James Bockheim; Josep G. Canadell; Eugenie Euskirchen; Christopher B. Field; Sergey V. Goryachkin; Stefan Hagemann; Peter Kuhry; Peter M. Lafleur; Hanna Lee; Galina Mazhitova; Frederick E. Nelson; Annette Rinke; Vladimir E. Romanovsky; Nikolay Shiklomanov; Charles Tarnocai; Sergey Venevsky; Jason G. Vogel; Sergei A. Zimov

2008-01-01

Thawing permafrost and the resulting microbial decomposition of previously frozen organic carbon (C) is one of the most significant potential feedbacks from terrestrial ecosystems to the atmosphere in a changing climate. In this article we present an overview of the global permafrost C pool and of the processes that might transfer this C into the atmosphere, as well as...

Global atmospheric changes.

OpenAIRE

Piver, W T

1991-01-01

Increasing concentrations of CO2 and other greenhouse gases in the atmosphere can be directly related to global warming. In terms of human health, because a major cause of increasing atmospheric concentrations of CO2 is the increased combustion of fossil fuels, global warming also may result in increases in air pollutants, acid deposition, and exposure to ultraviolet (UV) radiation. To understand better the impacts of global warming phenomena on human health, this review emphasizes the proces...

Atmospheric evidence for a global secular increase in carbon isotopic discrimination of land photosynthesis

Science.gov (United States)

Keeling, Ralph F.; Graven, Heather D.; Welp, Lisa R.; Resplandy, Laure; Bi, Jian; Piper, Stephen C.; Sun, Ying; Bollenbacher, Alane; Meijer, Harro A. J.

2017-09-01

A decrease in the 13C/12C ratio of atmospheric CO2 has been documented by direct observations since 1978 and from ice core measurements since the industrial revolution. This decrease, known as the 13C-Suess effect, is driven primarily by the input of fossil fuel-derived CO2 but is also sensitive to land and ocean carbon cycling and uptake. Using updated records, we show that no plausible combination of sources and sinks of CO2 from fossil fuel, land, and oceans can explain the observed 13C-Suess effect unless an increase has occurred in the 13C/12C isotopic discrimination of land photosynthesis. A trend toward greater discrimination under higher CO2 levels is broadly consistent with tree ring studies over the past century, with field and chamber experiments, and with geological records of C3 plants at times of altered atmospheric CO2, but increasing discrimination has not previously been included in studies of long-term atmospheric 13C/12C measurements. We further show that the inferred discrimination increase of 0.014 ± 0.007‰ ppm-1 is largely explained by photorespiratory and mesophyll effects. This result implies that, at the global scale, land plants have regulated their stomatal conductance so as to allow the CO2 partial pressure within stomatal cavities and their intrinsic water use efficiency to increase in nearly constant proportion to the rise in atmospheric CO2 concentration.

Global atmospheric changes.

Science.gov (United States)

Piver, W T

1991-12-01

Increasing concentrations of CO2 and other greenhouse gases in the atmosphere can be directly related to global warming. In terms of human health, because a major cause of increasing atmospheric concentrations of CO2 is the increased combustion of fossil fuels, global warming also may result in increases in air pollutants, acid deposition, and exposure to ultraviolet (UV) radiation. To understand better the impacts of global warming phenomena on human health, this review emphasizes the processes that are responsible for the greenhouse effect, air pollution, acid deposition, and increased exposure to UV radiation.

The Global Carbon Cycle: It's a Small World

Science.gov (United States)

Ineson, Philip; Milcu, Alexander; Subke, Jens-Arne; Wildman, Dennis; Anderson, Robert; Manning, Peter; Heinemeyer, Andreas

2010-05-01

Predicting future atmospheric concentrations of carbon dioxide (CO2), together with the impacts of these changes on global climate, are some of the most urgent and important challenges facing mankind. Modelling is the only way in which such predictions can be made, leading to the current generation of increasingly complex computer simulations, with associated concerns about embedded assumptions and conflicting model outputs. Alongside analysis of past climates, the GCMs currently represent our only hope of establishing the importance of potential runaway positive feedbacks linking climate change and atmospheric greenhouse gases yet the incorporation of necessary biospheric responses into GCMs markedly increases the uncertainty of predictions. Analysis of the importance of the major components of the global carbon (C) cycle reveals that an understanding of the conditions under which the terrestrial biosphere could switch from an overall carbon (C) sink to a source is critical to our ability to make future climate predictions. Here we present an alternative approach to assessing the short term biotic (plant and soil) sensitivities to elevated temperature and atmospheric CO2 through the use of a purely physical analogue. Centred on the concept of materially-closed systems containing scaled-down ratios of the global C stocks for the atmosphere, vegetation and soil we show that, in these model systems, the terrestrial biosphere is able to buffer a rise of 3oC even when coupled to very strong CO2-temperature positive feedbacks. The system respiratory response appears to be extremely well linked to temperature and is critical in deciding atmospheric concentrations of CO2. Simulated anthropogenic emissions of CO2 into the model systems showed an initial corresponding increase in atmospheric CO2 but, somewhat surprisingly, CO2 concentrations levelled off at ca. 480 p.p.m.v., despite continuing additions of CO2. Experiments were performed in which reversion of atmospheric

The global carbon budget 1959–2011

Directory of Open Access Journals (Sweden)

C. Le Quéré

2013-05-01

Full Text Available Accurate assessments of anthropogenic carbon dioxide (CO2 emissions and their redistribution among the atmosphere, ocean, and terrestrial biosphere is important to better understand the global carbon cycle, support the climate policy process, and project future climate change. Present-day analysis requires the combination of a range of data, algorithms, statistics and model estimates and their interpretation by a broad scientific community. Here we describe datasets and a methodology developed by the global carbon cycle science community to quantify all major components of the global carbon budget, including their uncertainties. We discuss changes compared to previous estimates, consistency within and among components, and methodology and data limitations. CO2 emissions from fossil fuel combustion and cement production (EFF are based on energy statistics, while emissions from Land-Use Change (ELUC, including deforestation, are based on combined evidence from land cover change data, fire activity in regions undergoing deforestation, and models. The global atmospheric CO2 concentration is measured directly and its rate of growth (GATM is computed from the concentration. The mean ocean CO2 sink (SOCEAN is based on observations from the 1990s, while the annual anomalies and trends are estimated with ocean models. Finally, the global residual terrestrial CO2 sink (SLAND is estimated by the difference of the other terms. For the last decade available (2002–2011, EFF was 8.3 ± 0.4 PgC yr−1, ELUC 1.0 ± 0.5 PgC yr−1, GATM 4.3 ± 0.1PgC yr−1, SOCEAN 2.5 ± 0.5 PgC yr−1, and SLAND 2.6 ± 0.8 PgC yr−1. For year 2011 alone, EFF was 9.5 ± 0.5 PgC yr−1, 3.0 percent above 2010, reflecting a continued trend in these emissions; ELUC was 0.9 ± 0.5 PgC yr−1, approximately constant throughout the decade; GATM was 3.6 ± 0.2 PgC yr−1, SOCEAN was 2.7 ± 0.5 PgC yr−1, and SLAND was 4.1 ± 0.9 PgC yr−1. GATM was low in 2011

Influence of variable rates of neritic carbonate deposition on atmospheric carbon dioxide and pelagic sediments

Science.gov (United States)

Walker, J. C.; Opdyke, B. C.

1995-01-01

Short-term imbalances in the global cycle of shallow water calcium carbonate deposition and dissolution may be responsible for much of the observed Pleistocene change in atmospheric carbon dioxide content. However, any proposed changes in the alkalinity balance of the ocean must be reconciled with the sedimentary record of deep-sea carbonates. The possible magnitude of the effect of shallow water carbonate deposition on the dissolution of pelagic carbonate can be tested using numerical simulations of the global carbon cycle. Boundary conditions can be defined by using extant shallow water carbonate accumulation data and pelagic carbonate deposition/dissolution data. On timescales of thousands of years carbonate deposition versus dissolution is rarely out of equilibrium by more than 1.5 x 10(13) mole yr-1. Results indicate that the carbonate chemistry of the ocean is rarely at equilibrium on timescales less than 10 ka. This disequilibrium is probably due to sea level-induced changes in shallow water calcium carbonate deposition/dissolution, an interpretation that does not conflict with pelagic sedimentary data from the central Pacific.

History of chemically and radiatively important atmospheric gases from the Advanced Global Atmospheric Gases Experiment (AGAGE

Directory of Open Access Journals (Sweden)

R. G. Prinn

2018-06-01

Full Text Available We present the organization, instrumentation, datasets, data interpretation, modeling, and accomplishments of the multinational global atmospheric measurement program AGAGE (Advanced Global Atmospheric Gases Experiment. AGAGE is distinguished by its capability to measure globally, at high frequency, and at multiple sites all the important species in the Montreal Protocol and all the important non-carbon-dioxide (non-CO2 gases assessed by the Intergovernmental Panel on Climate Change (CO2 is also measured at several sites. The scientific objectives of AGAGE are important in furthering our understanding of global chemical and climatic phenomena. They are the following: (1 to accurately measure the temporal and spatial distributions of anthropogenic gases that contribute the majority of reactive halogen to the stratosphere and/or are strong infrared absorbers (chlorocarbons, chlorofluorocarbons – CFCs, bromocarbons, hydrochlorofluorocarbons – HCFCs, hydrofluorocarbons – HFCs and polyfluorinated compounds (perfluorocarbons – PFCs, nitrogen trifluoride – NF3, sulfuryl fluoride – SO2F2, and sulfur hexafluoride – SF6 and use these measurements to determine the global rates of their emission and/or destruction (i.e., lifetimes; (2 to accurately measure the global distributions and temporal behaviors and determine the sources and sinks of non-CO2 biogenic–anthropogenic gases important to climate change and/or ozone depletion (methane – CH4, nitrous oxide – N2O, carbon monoxide – CO, molecular hydrogen – H2, methyl chloride – CH3Cl, and methyl bromide – CH3Br; (3 to identify new long-lived greenhouse and ozone-depleting gases (e.g., SO2F2, NF3, heavy PFCs (C4F10, C5F12, C6F14, C7F16, and C8F18 and hydrofluoroolefins (HFOs; e.g., CH2  =  CFCF3 have been identified in AGAGE, initiate the real-time monitoring of these new gases, and reconstruct their past histories from AGAGE, air archive, and firn air measurements; (4�

Carbon Disulfide (CS2) Mechanisms in Formation of Atmospheric Carbon Dioxide (CO2) Formation from Unconventional Shale Gas Extraction and Processing Operations and Global Climate Change.

Science.gov (United States)

Rich, Alisa L; Patel, Jay T

2015-01-01

Carbon disulfide (CS2) has been historically associated with the production of rayon, cellophane, and carbon tetrachloride. This study identifies multiple mechanisms by which CS2 contributes to the formation of CO2 in the atmosphere. CS2 and other associated sulfide compounds were found by this study to be present in emissions from unconventional shale gas extraction and processing (E&P) operations. The breakdown products of CS2; carbonyl sulfide (COS), carbon monoxide (CO), and sulfur dioxide (SO2) are indirect greenhouse gases (GHGs) that contribute to CO2 levels in the atmosphere. The heat-trapping nature of CO2 has been found to increase the surface temperature, resulting in regional and global climate change. The purpose of this study is to identify five mechanisms by which CS2 and the breakdown products of CS2 contribute to atmospheric concentrations of CO2. The five mechanisms of CO2 formation are as follows: Chemical Interaction of CS2 and hydrogen sulfide (H2S) present in natural gas at high temperatures, resulting in CO2 formation;Combustion of CS2 in the presence of oxygen producing SO2 and CO2;Photolysis of CS2 leading to the formation of COS, CO, and SO2, which are indirect contributors to CO2 formation;One-step hydrolysis of CS2, producing reactive intermediates and ultimately forming H2S and CO2;Two-step hydrolysis of CS2 forming the reactive COS intermediate that reacts with an additional water molecule, ultimately forming H2S and CO2. CS2 and COS additionally are implicated in the formation of SO2 in the stratosphere and/or troposphere. SO2 is an indirect contributor to CO2 formation and is implicated in global climate change.

Global assessment of promising forest management practices for sequestration of carbon

International Nuclear Information System (INIS)

Winjum, J.K.; Dixon, R.K.; Schroeder, P.E.

1991-01-01

In the 1980s, forests covered an estimated 4.08 billion hectares and contained a carbon pool of 1,400 gigatonnes, or 64% of the total terrestrial pool. Forest biomass productivity per unit of land can be enhanced by proper management practices and it is suggested that by implementing such practices, forests could store more carbon globally and thereby slow the increase in atmospheric CO 2 . Currently, only about 10% of world forests are managed at an active level. An assessment is presented of the amount of carbon that could be sequestered globally by implementing the practices of reforestation, afforestation, natural regeneration, silviculture, and agroforestry. The assessment is based on the development of a global database on managed forest and agroforestry systems. For each of the above five practices, the database contains information on carbon sequestered per hectare, implementation costs, and estimates of the amount of land technically suitable for such practices throughout the world. Results are presented for each practice in the boreal, temperate, and tropical regions. Preliminary estimates show that promising forestry and agroforestry practices could sequester, over a 50-y period, ca 50-100 gigatonnes of carbon at a cost of $170-340 million. This would be a significant contribution as a mitigating measure regarding atmospheric CO 2 buildup and projections for global warming, at present rates of anthropogenic carbon emissions (300-400 gigatonnes carbon over 50 y). 19 refs., 2 figs., 4 tabs

Global Carbon Reservoir Oxidative Ratios

Science.gov (United States)

Masiello, C. A.; Gallagher, M. E.; Hockaday, W. C.

2010-12-01

Photosynthesis and respiration move carbon and oxygen between the atmosphere and the biosphere at a ratio that is characteristic of the biogeochemical processes involved. This ratio is called the oxidative ratio (OR) of photosynthesis and respiration, and is defined as the ratio of moles of O2 per moles of CO2. This O2/CO2 ratio is a characteristic of biosphere-atmosphere gas fluxes, much like the 13C signature of CO2 transferred between the biosphere and the atmosphere has a characteristic signature. OR values vary on a scale of 0 (CO2) to 2 (CH4), with most ecosystem values clustered between 0.9 and 1.2. Just as 13C can be measured for both carbon fluxes and carbon pools, OR can also be measured for fluxes and pools and can provide information about the processes involved in carbon and oxygen cycling. OR values also provide information about reservoir organic geochemistry because pool OR values are proportional to the oxidation state of carbon (Cox) in the reservoir. OR may prove to be a particularly valuable biogeochemical tracer because of its ability to couple information about ecosystem gas fluxes with ecosystem organic geochemistry. We have developed 3 methods to measure the OR of ecosystem carbon reservoirs and intercalibrated them to assure that they yield accurate, intercomparable data. Using these tools we have built a large enough database of biomass and soil OR values that it is now possible to consider the implications of global patterns in ecosystem OR values. Here we present a map of the natural range in ecosystem OR values and begin to consider its implications. One striking pattern is an apparent offset between soil and biospheric OR values: soil OR values are frequently higher than that of their source biomass. We discuss this trend in the context of soil organic geochemistry and gas fluxes.

Nested atmospheric inversion for the terrestrial carbon sources and sinks in China

Directory of Open Access Journals (Sweden)

F. Jiang

2013-08-01

Full Text Available In this study, we establish a nested atmospheric inversion system with a focus on China using the Bayesian method. The global surface is separated into 43 regions based on the 22 TransCom large regions, with 13 small regions in China. Monthly CO2 concentrations from 130 GlobalView sites and 3 additional China sites are used in this system. The core component of this system is an atmospheric transport matrix, which is created using the TM5 model with a horizontal resolution of 3° × 2°. The net carbon fluxes over the 43 global land and ocean regions are inverted for the period from 2002 to 2008. The inverted global terrestrial carbon sinks mainly occur in boreal Asia, South and Southeast Asia, eastern America and southern South America. Most China areas appear to be carbon sinks, with strongest carbon sinks located in Northeast China. From 2002 to 2008, the global terrestrial carbon sink has an increasing trend, with the lowest carbon sink in 2002. The inter-annual variation (IAV of the land sinks shows remarkable correlation with the El Niño Southern Oscillation (ENSO. The terrestrial carbon sinks in China also show an increasing trend. However, the IAV in China is not the same as that of the globe. There is relatively stronger land sink in 2002, lowest sink in 2006, and strongest sink in 2007 in China. This IAV could be reasonably explained with the IAVs of temperature and precipitation in China. The mean global and China terrestrial carbon sinks over the period 2002–2008 are −3.20 ± 0.63 and −0.28 ± 0.18 PgC yr−1, respectively. Considering the carbon emissions in the form of reactive biogenic volatile organic compounds (BVOCs and from the import of wood and food, we further estimate that China's land sink is about −0.31 PgC yr−1.

TCCON Philippines: Towards Quantifying Atmospheric Carbon in Southeast Asia

Science.gov (United States)

Morino, I.; Velazco, V. A.; Uchino, O.; Schwandner, F. M.; Macatangay, R. C.; Nakatsuru, T.; Deutscher, N. M.; Belikov, D.; Maksyutov, S. S.; Oishi, Y.; Nakajima, T. Y.; Griffith, D. W. T.

2016-12-01

TCCON is dedicated to the precise measurements of greenhouse gases such as CO2 and CH4. TCCON measurements have been and are currently used extensively and globally for satellite validation, for comparison with atmospheric chemistry models and to study atmosphere-biosphere exchanges of carbon. With the global effort to cap greenhouse gas emissions, TCCON has taken on a vital role in validating satellite-based greenhouse gas data from past, current and future missions like Japanese GOSAT and GOSAT-2, NASA's OCO-2 and OCO-3, Chinese TanSat, and others. The lack of reliable validation data for the satellite-based greenhouse gas observing missions in the tropical regions is a common limitation in global carbon-cycle modeling studies that have a tropical component. The international CO2 modeling community has specified a requirement for "expansion of the CO2 observation network within the tropics" to reduce uncertainties in regional estimates of CO2 sources and sinks using atmospheric transport models. A TCCON site in the western tropical Pacific is a logical next step in obtaining additional knowledge that would greatly contribute to the understanding of the Earth's atmosphere and better constraining a major tropical region experiencing tremendous economic and population growth. Here, we present an assessment for a possible site in the Philippines where a new TCCON FTS will be installed. We also describe the newly constructed TCCON instrument intended for deployment to the Philippines and show a characterization of its performance and initial measurements at the NIES compound in Japan.

Combustion's impact on the global atmosphere

International Nuclear Information System (INIS)

Prather, M.J.; Logan, J.A.

1994-01-01

The combustion of a hydrocarbon fuel removes molecular oxygen (O 2 ) from the atmosphere and releases equivalent amounts of water (H 2 ) and carbon dioxide (CO 2 ), almost always with trace amounts of numerous other compounds including hydrocarbon (CH 4 , C 2 H 2 , C 2 H 4 , C 2 H 6 , C 3 H 8 , C 6 H 6 , CH 3 CHO, etc.), carbon monoxide (CO), nitrogen oxides (NO, N 2 O) and reduced nitrogen (NH 3 and HCN), sulfur gases (SO 2 , OCS, CS 2 ), halocarbons (CH 3 Al and CH 3 Br), and particles. A review of the atmospheric budgets of these gases shows that burning of fossil fuels and recent biomass has led to global alterations in the composition of the atmosphere. Combustion is clearly responsible for most of the enhanced greenhouse forcing to date (through CO 2 , tropospheric O 3 , soot) and also some counteracting effects (through SO 2 ). It has had minimal impact on stratospheric O 3 (through CH 3 Cl, CH 3 Br, CH 4 ), but has likely changed the tropospheric oxidant levels (through CO, NO x , NMHC), at least over the northern hemisphere. Most of the important greenhouse gases and tropospheric oxidant gases have significant natural sources, which are not well defined today and may be changing; and thus, quantifying the role of combustion is difficult. 113 refs

Atmospheric turbulence triggers pronounced diel pattern in karst carbonate geochemistry

Science.gov (United States)

Roland, M.; Serrano-Ortiz, P.; Kowalski, A. S.; Goddéris, Y.; Sánchez-Cañete, E. P.; Ciais, P.; Domingo, F.; Cuezva, S.; Sanchez-Moral, S.; Longdoz, B.; Yakir, D.; Van Grieken, R.; Schott, J.; Cardell, C.; Janssens, I. A.

2013-07-01

CO2 exchange between terrestrial ecosystems and the atmosphere is key to understanding the feedbacks between climate change and the land surface. In regions with carbonaceous parent material, CO2 exchange patterns occur that cannot be explained by biological processes, such as disproportionate outgassing during the daytime or nighttime CO2 uptake during periods when all vegetation is senescent. Neither of these phenomena can be attributed to carbonate weathering reactions, since their CO2 exchange rates are too small. Soil ventilation induced by high atmospheric turbulence is found to explain atypical CO2 exchange between carbonaceous systems and the atmosphere. However, by strongly altering subsurface CO2 concentrations, ventilation can be expected to influence carbonate weathering rates. By imposing ventilation-driven CO2 outgassing in a carbonate weathering model, we show here that carbonate geochemistry is accelerated and does play a surprisingly large role in the observed CO2 exchange pattern of a semi-arid ecosystem. We found that by rapidly depleting soil CO2 during the daytime, ventilation disturbs soil carbonate equilibria and therefore strongly magnifies daytime carbonate precipitation and associated CO2 production. At night, ventilation ceases and the depleted CO2 concentrations increase steadily. Dissolution of carbonate is now enhanced, which consumes CO2 and largely compensates for the enhanced daytime carbonate precipitation. This is why only a relatively small effect on global carbonate weathering rates is to be expected. On the short term, however, ventilation has a drastic effect on synoptic carbonate weathering rates, resulting in a pronounced diel pattern that exacerbates the non-biological behavior of soil-atmosphere CO2 exchanges in dry regions with carbonate soils.

Effects of fuel and forest conservation on future levels of atmospheric carbon dioxide.

Science.gov (United States)

Walker, J C; Kasting, J F

1992-01-01

We develop a numerical simulation of the global biogeochemical cycles of carbon that works over time scales extending from years to millions of years. The ocean is represented by warm and cold shallow water reservoirs, a thermocline reservoir, and deep Atlantic, Indian, and Pacific reservoirs. The atmosphere is characterized by a single carbon reservoir and the global biota by a single biomass reservoir. The simulation includes the rock cycle, distinguishing between shelf carbonate and pelagic carbonate precipitation, with distinct lysocline depths in the three deep ocean reservoirs. Dissolution of pelagic carbonates in response to decrease in lysocline depth is included. The simulation is tuned to reproduce the observed radiocarbon record resulting from atomic weapon testing. It is tuned also to reproduce the distribution of dissolved phosphate and total dissolved carbon between the ocean reservoirs as well as the carbon isotope ratios for both 13C and 14C in ocean and atmosphere. The simulation reproduces reasonably well the historical record of carbon dioxide partial pressure as well as the atmospheric isotope ratios for 13C and 14C over the last 200 yr as these have changed in response to fossil fuel burning and land use changes, principally forest clearance. The agreements between observation and calculation involves the assumption of a carbon dioxide fertilization effect in which the rate of production of biomass increases with increasing carbon dioxide partial pressure. At present the fertilization effect of increased carbon dioxide outweighs the effects of forest clearance, so the biota comprises an overall sink of atmospheric carbon dioxide sufficiently large to bring the budget approximately into balance. This simulation is used to examine the future evolution of carbon dioxide and its sensitivity to assumptions about the rate of fossil fuel burning and of forest clearance. Over times extending up to thousands of years, the results are insensitive to the

Global impact of carbon-14 from nuclear power reactors

International Nuclear Information System (INIS)

Moghissi, A.A.; Carter, M.W.

1977-01-01

Carbon-14 is produced by nuclear power reactors, predominently as a result of the interaction of a neutron and nitrogen-14 both in the fuel and in the coolant. Several other reactions also contribute to the production of carbon-14. Present operational procedures, in general, for reactors and fuel reprocessing plants result in the release of carbon-14 into the environment. Combustion of fossil fuels and certain industrial operations contribute to the supply of CO 2 in the atmosphere and this contribution is essentially free of carbon-14. Future carbon-14 burdens by assuming a thorough mixing of all CO 2 in the atmosphere is predicted. Available data on electric power generation, fossil fuel combustion and certain other information are used to calculate the projected specific activity of carbon-14 by the year 2000 and the twenty-first century. According to these calculations, the global population dose from carbon-14 can be substantial. Also, carbon-14 in the vicinity of nuclear power reactors is considered. Because of the chemistry of carbon-14, it is shown that local problems may be more significant around BWR's as compared to PWR's. Based on environmental considerations of carbon-14, its increasing production and discharge into the atmosphere, and available control technology, it is recommended that nitrogen use and its presence be minimized in pertinent reactor components and operations

Modeling the dynamics of carbon dioxide removal in the atmosphere

Directory of Open Access Journals (Sweden)

Shyam Sundar

2014-12-01

Full Text Available The temperature of Earth's surface is increasing over the past few years due to emission of global warming gases such as CO2, CH4 and NOx from industries, power plants, etc., leading to several adverse effects on human and his environment. Therefore, the question of their removal/reduction from the atmosphere is very important. In this paper, a nonlinear mathematical model to study the removal/reduction of carbon dioxide by using suitable absorbent (such as aqueous ammonia solution, amines, sodium hydroxide, etc. near the source of emission and externally introducing liquid species in the atmosphere is presented. Dynamical properties of the model which include local and global stabilities for the equilibrium are analyzed carefully. Model analysis is performed by considering three physical situations i.e. when both absorbent and the liquid species are used, only absorbent is used and only liquid species is used. It is shown that the concentration of carbon dioxide decreases as the rate of introduction of absorbent in the absorber increases. It decreases further as the rate of introduction of liquid species. Thus, the concentration of carbon dioxide would be reduced by a large amount if adequate amount of absorbent is used near the source of emission. The remaining amount can be reduced further by infusing liquid drops in the atmosphere. Numerical simulations are also carried out to support the analytical results.

Biodiversity Meets the Atmosphere: A Global View of Forest Canopies

Science.gov (United States)

C. M. P. Ozanne; D. Anhuf; S. L. Boulter; M. Keller; R. L. Kitching; C. Korner; F. C. Meinzer; A. W. Mitchell; T. Nakashizuka; P. L. Silva Dias; N. E. Stork; S. J. Wright; M Yoshimura

2003-01-01

The forest canopy is the functional interface between 90% of Earth’s terrestrial biomass and the atmosphere. Multidisciplinary research in the canopy has expanded concepts of global species richness, physiological processes, and the provision of ecosystem services. Trees respond in a species-specific manner to elevated carbon dioxide levels, while climate change...

Incorrectly Interpreting the Carbon Mass Balance Technique Leads to Biased Emissions Estimates from Global Vegetation Fires

Science.gov (United States)

Surawski, N. C.; Sullivan, A. L.; Roxburgh, S. H.; Meyer, M.; Polglase, P. J.

2016-12-01

Vegetation fires are a complex phenomenon and have a range of global impacts including influences on climate. Even though fire is a necessary disturbance for the maintenance of some ecosystems, a range of anthropogenically deleterious consequences are associated with it, such as damage to assets and infrastructure, loss of life, as well as degradation to air quality leading to negative impacts on human health. Estimating carbon emissions from fire relies on a carbon mass balance technique which has evolved with two different interpretations in the fire emissions community. Databases reporting global fire emissions estimates use an approach based on `consumed biomass' which is an approximation to the biogeochemically correct `burnt carbon' approach. Disagreement between the two methods occurs because the `consumed biomass' accounting technique assumes that all burnt carbon is volatilized and emitted. By undertaking a global review of the fraction of burnt carbon emitted to the atmosphere, we show that the `consumed biomass' accounting approach overestimates global carbon emissions by 4.0%, or 100 Teragrams, annually. The required correction is significant and represents 9% of the net global forest carbon sink estimated annually. To correctly partition burnt carbon between that emitted to the atmosphere and that remaining as a post-fire residue requires the post-burn carbon content to be estimated, which is quite often not undertaken in atmospheric emissions studies. To broaden our understanding of ecosystem carbon fluxes, it is recommended that the change in carbon content associated with burnt residues be accounted for. Apart from correctly partitioning burnt carbon between the emitted and residue pools, it enables an accounting approach which can assess the efficacy of fire management operations targeted at sequestering carbon from fire. These findings are particularly relevant for the second commitment period for the Kyoto protocol, since improved landscape fire

Soils and Global Change in the Carbon Cycle over Geological Time

Science.gov (United States)

Retallack, G. J.

2003-12-01

Soils play an important role in the carbon cycle as the nutrition of photosynthesized biomass. Nitrogen fixed by microbes from air is a limiting nutrient for ecosystems within the first flush of ecological succession of new ground, and sulfur can limit some components of wetland ecosystems. But over the long term, the limiting soil nutrient is phosphorus extracted by weathering from minerals such as apatite (Vitousek et al., 1997a; Chadwick et al., 1999). Life has an especially voracious appetite for common alkali (Na+ and K+) and alkaline earth (Ca2+ and Mg2+) cations, supplied by hydrolytic weathering, which is in turn amplified by biological acidification (Schwartzmann and Volk, 1991; see Chapter 5.06). These mineral nutrients fuel photosynthetic fixation and chemical reduction of atmospheric CO2 into plants and plantlike microbes, which are at the base of the food chain. Plants and photosynthetic microbes are consumed and oxidized by animals, fungi, and other respiring microbes, which release CO2, methane, and water vapor to the air. These greenhouse gases absorb solar radiation more effectively than atmospheric oxygen and nitrogen, and are important regulators of planetary temperature and albedo (Kasting, 1992). Variations in solar insolation ( Kasting, 1992), mountainous topography ( Raymo and Ruddiman, 1992), and ocean currents ( Ramstein et al., 1997) also play a role in climate, but this review focuses on the carbon cycle. The carbon cycle is discussed in detail in Volume 8 of this Treatise.The greenhouse model for global paleoclimate has proven remarkably robust (Retallack, 2002), despite new challenges ( Veizer et al., 2000). The balance of producers and consumers is one of a number of controls on atmospheric greenhouse gas balance, because CO2 is added to the air from fumaroles, volcanic eruptions, and other forms of mantle degassing (Holland, 1984). Carbon dioxide is also consumed by burial as carbonate and organic matter within limestones and other

Global Atmosphere Watch Workshop on Measurement-Model Fusion for Global Total Atmospheric Deposition (MMF-GTAD)

Science.gov (United States)

The World Meteorological Organization’s (WMO) Global Atmosphere Watch (GAW) Programme coordinates high-quality observations of atmospheric composition from global to local scales with the aim to drive high-quality and high-impact science while co-producing a new generation of pro...

Soil carbon model alternatives for ECHAM5/JSBACH climate model: Evaluation and impacts on global carbon cycle estimates

DEFF Research Database (Denmark)

Thum, T.; Raisanen, P.; Sevanto, S.

2011-01-01

The response of soil organic carbon to climate change might lead to significant feedbacks affecting global warming. This response can be studied by coupled climate-carbon cycle models but so far the description of soil organic carbon cycle in these models has been quite simple. In this work we used...... the coupled climate-carbon cycle model ECHAM5/JSBACH (European Center/Hamburg Model 5/Jena Scheme for Biosphere-Atmosphere Coupling in Hamburg) with two different soil carbon modules, namely (1) the original soil carbon model of JSBACH called CBALANCE and (2) a new soil carbon model Yasso07, to study...... the interaction between climate variability and soil organic carbon. Equivalent ECHAM5/JSBACH simulations were conducted using both soil carbon models, with freely varying atmospheric CO2 for the last 30 years (1977-2006). In this study, anthropogenic CO2 emissions and ocean carbon cycle were excluded. The new...

Global Atmosphere Watch Workshop on Measurement-Model ...

Science.gov (United States)

The World Meteorological Organization’s (WMO) Global Atmosphere Watch (GAW) Programme coordinates high-quality observations of atmospheric composition from global to local scales with the aim to drive high-quality and high-impact science while co-producing a new generation of products and services. In line with this vision, GAW’s Scientific Advisory Group for Total Atmospheric Deposition (SAG-TAD) has a mandate to produce global maps of wet, dry and total atmospheric deposition for important atmospheric chemicals to enable research into biogeochemical cycles and assessments of ecosystem and human health effects. The most suitable scientific approach for this activity is the emerging technique of measurement-model fusion for total atmospheric deposition. This technique requires global-scale measurements of atmospheric trace gases, particles, precipitation composition and precipitation depth, as well as predictions of the same from global/regional chemical transport models. The fusion of measurement and model results requires data assimilation and mapping techniques. The objective of the GAW Workshop on Measurement-Model Fusion for Global Total Atmospheric Deposition (MMF-GTAD), an initiative of the SAG-TAD, was to review the state-of-the-science and explore the feasibility and methodology of producing, on a routine retrospective basis, global maps of atmospheric gas and aerosol concentrations as well as wet, dry and total deposition via measurement-model

Ozone, Climate, and Global Atmospheric Change.

Science.gov (United States)

Levine, Joel S.

1992-01-01

Presents an overview of global atmospheric problems relating to ozone depletion and global warming. Provides background information on the composition of the earth's atmosphere and origin of atmospheric ozone. Describes causes, effects, and evidence of ozone depletion and the greenhouse effect. A vignette provides a summary of a 1991 assessment of…

Joint Application of Concentrations and Isotopic Signatures to Investigate the Global Atmospheric Carbon Monoxide Budget: Inverse Modeling Approach

Science.gov (United States)

Park, K.; Mak, J. E.; Emmons, L. K.

2008-12-01

Carbon monoxide is not only an important component for determining the atmospheric oxidizing capacity but also a key trace gas in the atmospheric chemistry of the Earth's background environment. The global CO cycle and its change are closely related to both the change of CO mixing ratio and the change of source strength. Previously, to estimate the global CO budget, most top-down estimation techniques have been applied the concentrations of CO solely. Since CO from certain sources has a unique isotopic signature, its isotopes provide additional information to constrain its sources. Thus, coupling the concentration and isotope fraction information enables to tightly constrain CO flux by its sources and allows better estimations on the global CO budget. MOZART4 (Model for Ozone And Related chemical Tracers), a 3-D global chemical transport model developed at NCAR, MPI for meteorology and NOAA/GFDL and is used to simulate the global CO concentration and its isotopic signature. Also, a tracer version of MOZART4 which tagged for C16O and C18O from each region and each source was developed to see their contributions to the atmosphere efficiently. Based on the nine-year-simulation results we analyze the influences of each source of CO to the isotopic signature and the concentration. Especially, the evaluations are focused on the oxygen isotope of CO (δ18O), which has not been extensively studied yet. To validate the model performance, CO concentrations and isotopic signatures measured from MPI, NIWA and our lab are compared to the modeled results. The MOZART4 reproduced observational data fairly well; especially in mid to high latitude northern hemisphere. Bayesian inversion techniques have been used to estimate the global CO budget with combining observed and modeled CO concentration. However, previous studies show significant differences in their estimations on CO source strengths. Because, in addition to the CO mixing ratio, isotopic signatures are independent tracers

A secular carbon debt from atmospheric high temperature combustion of stem wood?

DEFF Research Database (Denmark)

Czeskleba-Dupont, Rolf

2012-01-01

' approach for smokestack emissions that was propagated within the Kyoto process, the first phase of which is terminating in 2012. Otherwise, it is tolerated that the substitution of wood pellets for coal or other fossil fuels creates long lasting extra emissions of carbon dioxide – a mistake of climate......Basically, combustion of woody biomass in high temperature processes that react with atmospheric air results in a long lasting addition of carbon dioxide to the atmosphere. When harvesting large extra amounts of stem tree for energetic use, a global as well as secular time frame is needed to assess...... overall consequences with due attention given to biosphere processes, including the complex productivity of whole ecosystems. Analytically, a time dependent variable of carbon neutralization can be traced by a simple carbon neutrality or CN factor. Using the forgotten Marland approach, project managers...

CARBON NEUTRON STAR ATMOSPHERES

International Nuclear Information System (INIS)

Suleimanov, V. F.; Klochkov, D.; Werner, K.; Pavlov, G. G.

2014-01-01

The accuracy of measuring the basic parameters of neutron stars is limited in particular by uncertainties in the chemical composition of their atmospheres. For example, the atmospheres of thermally emitting neutron stars in supernova remnants might have exotic chemical compositions, and for one of them, the neutron star in Cas A, a pure carbon atmosphere has recently been suggested by Ho and Heinke. To test this composition for other similar sources, a publicly available detailed grid of the carbon model atmosphere spectra is needed. We have computed this grid using the standard local thermodynamic equilibrium approximation and assuming that the magnetic field does not exceed 10 8  G. The opacities and pressure ionization effects are calculated using the Opacity Project approach. We describe the properties of our models and investigate the impact of the adopted assumptions and approximations on the emergent spectra

The carbon cycle in a land surface model: modelling, validation and implementation at a global scale; Cycle du carbone dans un modele de surface continentale: modelisation, validation et mise en oeuvre a l'echelle globale

Energy Technology Data Exchange (ETDEWEB)

Gibelin, A L

2007-05-15

ISBA-A-gs is an option of the CNRM land surface model ISBA which allows for the simulation of carbon exchanges between the terrestrial biosphere and the atmosphere. The model was implemented for the first time at the global scale as a stand-alone model. Several global simulations were performed to assess the sensitivity of the turbulent fluxes and Leaf Area Index to a doubling of the CO{sub 2} atmospheric concentration, and to the climate change simulated by the end of the 21. century. In addition, a new option of ISBA, referred to as ISBA-CC, was developed in order to simulate a more detailed ecosystem respiration by separating the autotrophic respiration and the heterotrophic respiration. The vegetation dynamics and the carbon fluxes were validated at a global scale using satellite datasets, and at a local scale using data from 26 sites of the FLUXNET network. All these results show that the model is sufficiently realistic to be coupled with a general circulation model, in order to account for interactions between the terrestrial biosphere, the atmosphere and the carbon cycle. (author)

Particulate carbon in the atmosphere

International Nuclear Information System (INIS)

Surakka, J.

1992-01-01

Carbonaceous aerosols are emitted to the atmosphere in combustion processes. Carbon particles are very small and have a long residence time in the air. Black Carbon, a type of carbon aerosol, is a good label when transport of combustion emissions in the atmosphere is studied. It is also useful tool in air quality studies. Carbon particles absorb light 6.5 to 8 times stronger than any other particulate matter in the air. Their effect on decreasing visibility is about 50 %. Weather disturbances are also caused by carbon emissions e.g. in Kuwait. Carbon particles have big absorption surface and capacity to catalyze different heterogenous reactions in air. Due to their special chemical and physical properties particulate carbon is a significant air pollution specie, especially in urban air. Average particulate carbon concentration of 5.7 μg/m 2 have been measured in winter months in Helsinki

Diffusion-type model of the global carbon cycle for the estimation of dose to the world population from releases of carbon-14 to the atmosphere

International Nuclear Information System (INIS)

Killough, G.G.

1977-05-01

A nonlinear dynamic model of the exchange of carbon among the atmosphere, terrestrial biosphere, and ocean is described and applied to estimating the radiation dose to the world's population from the release of 14 C to the atmosphere from the nuclear power industry. A computer implementation of the model, written in the IBM Continuous System Modeling Program III (CSMP III) simulation language, is presented. The model treats the ocean as a diffusive medium with respect to vertical transport of carbon, and the nonlinear variation of CO 2 partial pressure with the total inorganic carbon concentration in surface waters is taken into account in calculating the transfer rate from ocean to atmosphere. Transfers between the atmosphere and terrestrial biosphere are represented by nonlinear equations which consider CO 2 fertilization and impose a constraint on the ultimate total carbon mass in the biosphere

Global variation of carbon use efficiency in terrestrial ecosystems

Science.gov (United States)

Tang, Xiaolu; Carvalhais, Nuno; Moura, Catarina; Reichstein, Markus

2017-04-01

Carbon use efficiency (CUE), defined as the ratio between net primary production (NPP) and gross primary production (GPP), is an emergent property of vegetation that describes its effectiveness in storing carbon (C) and is of significance for understanding C biosphere-atmosphere exchange dynamics. A constant CUE value of 0.5 has been widely used in terrestrial C-cycle models, such as the Carnegie-Ames-Stanford-Approach model, or the Marine Biological Laboratory/Soil Plant-Atmosphere Canopy Model, for regional or global modeling purposes. However, increasing evidence argues that CUE is not constant, but varies with ecosystem types, site fertility, climate, site management and forest age. Hence, the assumption of a constant CUE of 0.5 can produce great uncertainty in estimating global carbon dynamics between terrestrial ecosystems and the atmosphere. Here, in order to analyze the global variations in CUE and understand how CUE varies with environmental variables, a global database was constructed based on published data for crops, forests, grasslands, wetlands and tundra ecosystems. In addition to CUE data, were also collected: GPP and NPP; site variables (e.g. climate zone, site management and plant function type); climate variables (e.g. temperature and precipitation); additional carbon fluxes (e.g. soil respiration, autotrophic respiration and heterotrophic respiration); and carbon pools (e.g. stem, leaf and root biomass). Different climate metrics were derived to diagnose seasonal temperature (mean annual temperature, MAT, and maximum temperature, Tmax) and water availability proxies (mean annual precipitation, MAP, and Palmer Drought Severity Index), in order to improve the local representation of environmental variables. Additionally were also included vegetation phenology dynamics as observed by different vegetation indices from the MODIS satellite. The mean CUE of all terrestrial ecosystems was 0.45, 10% lower than the previous assumed constant CUE of 0

Terrestrial nitrogen-carbon cycle interactions at the global scale.

Science.gov (United States)

Zaehle, S

2013-07-05

Interactions between the terrestrial nitrogen (N) and carbon (C) cycles shape the response of ecosystems to global change. However, the global distribution of nitrogen availability and its importance in global biogeochemistry and biogeochemical interactions with the climate system remain uncertain. Based on projections of a terrestrial biosphere model scaling ecological understanding of nitrogen-carbon cycle interactions to global scales, anthropogenic nitrogen additions since 1860 are estimated to have enriched the terrestrial biosphere by 1.3 Pg N, supporting the sequestration of 11.2 Pg C. Over the same time period, CO2 fertilization has increased terrestrial carbon storage by 134.0 Pg C, increasing the terrestrial nitrogen stock by 1.2 Pg N. In 2001-2010, terrestrial ecosystems sequestered an estimated total of 27 Tg N yr(-1) (1.9 Pg C yr(-1)), of which 10 Tg N yr(-1) (0.2 Pg C yr(-1)) are due to anthropogenic nitrogen deposition. Nitrogen availability already limits terrestrial carbon sequestration in the boreal and temperate zone, and will constrain future carbon sequestration in response to CO2 fertilization (regionally by up to 70% compared with an estimate without considering nitrogen-carbon interactions). This reduced terrestrial carbon uptake will probably dominate the role of the terrestrial nitrogen cycle in the climate system, as it accelerates the accumulation of anthropogenic CO2 in the atmosphere. However, increases of N2O emissions owing to anthropogenic nitrogen and climate change (at a rate of approx. 0.5 Tg N yr(-1) per 1°C degree climate warming) will add an important long-term climate forcing.

Atmospheric redistribution of reactive nitrogen and phosphorus by wildfires and implications for global carbon cycling

Science.gov (United States)

Randerson, J. T.; Xu, L.; Wiggins, E. B.; Chen, Y.; Riley, W. J.; Mekonnen, Z. A.; Pellegrini, A.; Mahowald, N. M.

2017-12-01

Fires are an important process regulating the redistribution of nutrients within terrestrial ecosystems. Frequently burning ecosystems such as savannas are a net source of N and P to the atmosphere each year, with atmospheric transport and dry and wet deposition increasing nutrient availability in downwind ecosystems and over the open ocean. Transport of N and P aerosols from savanna fires within the Hadley circulation contributes to nutrient deposition over tropical forests, yielding an important cross-biome nutrient transfer. Pyrodenitrification of reactive N increases with fire temperature and modified combustion efficiency, generating a global net biospheric loss of approximately 14 Tg N per year. Here we analyze atmospheric N and P redistribution using the Global Fire Emissions Database version 4s and the Accelerated Climate Modeling for Energy earth system model. We synthesize literature estimates of N and P concentrations in fire-emitted aerosols and ecosystem mass balance measurements to help constrain model estimates of these biosphere-atmosphere fluxes. In our analysis, we estimate the fraction of terrestrial net primary production (NPP) that is sustained by fire-emitted P and reactive N from upwind ecosystems. We then evaluate how recent global declines in burned area in savanna and grassland ecosystems may be changing nutrient availability in downwind ecosystems.

The carbon cycle in a land surface model: modelling, validation and implementation at a global scale; Cycle du carbone dans un modele de surface continentale: modelisation, validation et mise en oeuvre a l'echelle globale

Energy Technology Data Exchange (ETDEWEB)

Gibelin, A.L

2007-05-15

ISBA-A-gs is an option of the CNRM land surface model ISBA which allows for the simulation of carbon exchanges between the terrestrial biosphere and the atmosphere. The model was implemented for the first time at the global scale as a stand-alone model. Several global simulations were performed to assess the sensitivity of the turbulent fluxes and Leaf Area Index to a doubling of the CO{sub 2} atmospheric concentration, and to the climate change simulated by the end of the 21. century. In addition, a new option of ISBA, referred to as ISBA-CC, was developed in order to simulate a more detailed ecosystem respiration by separating the autotrophic respiration and the heterotrophic respiration. The vegetation dynamics and the carbon fluxes were validated at a global scale using satellite datasets, and at a local scale using data from 26 sites of the FLUXNET network. All these results show that the model is sufficiently realistic to be coupled with a general circulation model, in order to account for interactions between the terrestrial biosphere, the atmosphere and the carbon cycle. (author)

Atmospheric carbon reduction by urban trees

International Nuclear Information System (INIS)

Nowak, D.J.

1993-01-01

Trees, because they sequester atmospheric carbon through their growth process and conserve energy in urban areas, have been suggested as one means to combat increasing levels of atmospheric carbon. Analysis of the urban forest in Oakland, California (21% tree cover), reveals a tree carbon storage level of 11·0 metric tons/hectare. Trees in the area of the 1991 fire in Oakland stored approximately 14,500 metric tons of carbon, 10% of the total amount stored by Oakland's urban forest. National urban forest carbon storage in the United States (28% tree cover) is estimated at between 350 and 750 million metric tons. Establishment of 10 million urban trees annually over the next 10 years is estimated to sequester and offset the production of 363 million metric tons of carbon over the next 50 years-less than 1% of the estimated carbon emissions in the United States over the same time period. Advantages and limitations of managing urban trees to reduce atmospheric carbon are discussed. 36 refs., 2 figs., 3 tabs

Global carbon inequality

Energy Technology Data Exchange (ETDEWEB)

Hubacek, Klaus [University of Maryland, Department of Geographical Sciences, College Park, MD (United States); Masaryk University, Department of Environmental Studies, Brno (Czech Republic); Baiocchi, Giovanni [University of Maryland, Department of Geographical Sciences, College Park, MD (United States); University of Maryland, Department of Economics, College Park, MD (United States); Feng, Kuishuang [University of Maryland, Department of Geographical Sciences, College Park, MD (United States); Munoz Castillo, Raul [University of Maryland, Department of Geographical Sciences, College Park, MD (United States); Interamerican Development Bank, Washington, DC (United States); Sun, Laixiang [University of Maryland, Department of Geographical Sciences, College Park, MD (United States); SOAS, University of London, London (United Kingdom); International Institute for Applied Systems Analysis (IIASA), Laxenburg (Austria); Xue, Jinjun [Nagoya University, Graduate School of Economics, Nagoya (Japan); Hubei University of Economics, Wuhan (China)

2017-12-01

Global climate change and inequality are inescapably linked both in terms of who contributes climate change and who suffers the consequences. This fact is also partly reflected in two United Nations (UN) processes: on the one hand, the Paris Agreement of the UN Framework Convention on Climate Change under which countries agreed to hold the increase in the global average temperature to below 2 C above pre-industrial levels and, on the other hand, the UN's Sustainable Development Goals aiming to end poverty. These agreements are seen as important foundation to put the world nations on a sustainable pathway. However, how these agreements can be achieved or whether they are even mutually compatible is less clear. We explore the global carbon inequality between and within countries and the carbon implications of poverty alleviation by combining detailed consumer expenditure surveys for different income categories for a wide range of countries with an environmentally extended multi-regional input-output approach to estimate carbon footprints of different household groups, globally, and assess the carbon implications of moving the poorest people out of poverty. Given the current context, increasing income leads to increasing carbon footprints and makes global targets for mitigating greenhouse gases more difficult to achieve given the pace of technological progress and current levels of fossil fuel dependence. We conclude that the huge level of carbon inequality requires a critical discussion of undifferentiated income growth. Current carbon-intensive lifestyles and consumption patterns need to enter the climate discourse to a larger extent. (orig.)

Global carbon inequality

International Nuclear Information System (INIS)

Hubacek, Klaus; Baiocchi, Giovanni; Feng, Kuishuang; Munoz Castillo, Raul; Sun, Laixiang; Xue, Jinjun

2017-01-01

Global climate change and inequality are inescapably linked both in terms of who contributes climate change and who suffers the consequences. This fact is also partly reflected in two United Nations (UN) processes: on the one hand, the Paris Agreement of the UN Framework Convention on Climate Change under which countries agreed to hold the increase in the global average temperature to below 2 C above pre-industrial levels and, on the other hand, the UN's Sustainable Development Goals aiming to end poverty. These agreements are seen as important foundation to put the world nations on a sustainable pathway. However, how these agreements can be achieved or whether they are even mutually compatible is less clear. We explore the global carbon inequality between and within countries and the carbon implications of poverty alleviation by combining detailed consumer expenditure surveys for different income categories for a wide range of countries with an environmentally extended multi-regional input-output approach to estimate carbon footprints of different household groups, globally, and assess the carbon implications of moving the poorest people out of poverty. Given the current context, increasing income leads to increasing carbon footprints and makes global targets for mitigating greenhouse gases more difficult to achieve given the pace of technological progress and current levels of fossil fuel dependence. We conclude that the huge level of carbon inequality requires a critical discussion of undifferentiated income growth. Current carbon-intensive lifestyles and consumption patterns need to enter the climate discourse to a larger extent. (orig.)

Enhanced transfer of terrestrially derived carbon to the atmosphere in a flooding event

Science.gov (United States)

Bianchi, Thomas S.; Garcia-Tigreros, Fenix; Yvon-Lewis, Shari A.; Shields, Michael; Mills, Heath J.; Butman, David; Osburn, Christopher; Raymond, Peter A.; Shank, G. Christopher; DiMarco, Steven F.; Walker, Nan; Kiel Reese, Brandi; Mullins-Perry, Ruth; Quigg, Antonietta; Aiken, George R.; Grossman, Ethan L.

2013-01-01

Rising CO2 concentration in the atmosphere, global climate change, and the sustainability of the Earth's biosphere are great societal concerns for the 21st century. Global climate change has, in part, resulted in a higher frequency of flooding events, which allow for greater exchange between soil/plant litter and aquatic carbon pools. Here we demonstrate that the summer 2011 flood in the Mississippi River basin, caused by extreme precipitation events, resulted in a “flushing” of terrestrially derived dissolved organic carbon (TDOC) to the northern Gulf of Mexico. Data from the lower Atchafalaya and Mississippi rivers showed that the DOC flux to the northern Gulf of Mexico during this flood was significantly higher than in previous years. We also show that consumption of radiocarbon-modern TDOC by bacteria in floodwaters in the lower Atchafalaya River and along the adjacent shelf contributed to northern Gulf shelf waters changing from a net sink to a net source of CO2 to the atmosphere in June and August 2011. This work shows that enhanced flooding, which may or may not be caused by climate change, can result in rapid losses of stored carbon in soils to the atmosphere via processes in aquatic ecosystems.

Contribution of soil respiration to the global carbon equation.

Science.gov (United States)

Xu, Ming; Shang, Hua

2016-09-20

Soil respiration (Rs) is the second largest carbon flux next to GPP between the terrestrial ecosystem (the largest organic carbon pool) and the atmosphere at a global scale. Given their critical role in the global carbon cycle, Rs measurement and modeling issues have been well reviewed in previous studies. In this paper, we briefly review advances in soil organic carbon (SOC) decomposition processes and the factors affecting Rs. We examine the spatial and temporal distribution of Rs measurements available in the literature and found that most of the measurements were conducted in North America, Europe, and East Asia, with major gaps in Africa, East Europe, North Asia, Southeast Asia, and Australia, especially in dry ecosystems. We discuss the potential problems of measuring Rs on slope soils and propose using obliquely-cut soil collars to solve the existing problems. We synthesize previous estimates of global Rs flux and find that the estimates ranged from 50 PgC/yr to 98 PgC/yr and the error associated with each estimation was also high (4 PgC/yr to 33.2 PgC/yr). Using a newly integrated database of Rs measurements and the MODIS vegetation map, we estimate that the global annual Rs flux is 94.3 PgC/yr with an estimation error of 17.9 PgC/yr at a 95% confidence level. The uneven distribution of Rs measurements limits our ability to improve the accuracy of estimation. Based on the global estimation of Rs flux, we found that Rs is highly correlated with GPP and NPP at the biome level, highlighting the role of Rs in global carbon budgets. Copyright © 2016. Published by Elsevier GmbH.

Modeling of the global carbon cycle - isotopic data requirements

International Nuclear Information System (INIS)

Ciais, P.

1994-01-01

Isotopes are powerful tools to constrain carbon cycle models. For example, the combinations of the CO 2 and the 13 C budget allows to calculate the net-carbon fluxes between atmosphere, ocean, and biosphere. Observations of natural and bomb-produced radiocarbon allow to estimate gross carbon exchange fluxes between different reservoirs and to deduce time scales of carbon overturning in important reservoirs. 18 O in CO 2 is potentially a tool to make the deconvolution of C fluxes within the land biosphere (assimilation vs respirations). The scope of this article is to identify gaps in our present knowledge about isotopes in the light of their use as constraint for the global carbon cycle. In the following we will present a list of some future data requirements for carbon cycle models. (authors)

Monthly, global emissions of carbon dioxide from fossil fuel consumption

Energy Technology Data Exchange (ETDEWEB)

Andres, R. J.; Marland, G.; Boden, T. A. (Environmental Sciences Div., Oak Ridge National Laboratory, Oak Ridge, TN (United States)), e-mail: andresrj@ornl.gov; Gregg, J. S. (Risoe DTU National Laboratory for Sustainable Energy, Roskilde (Denmark)); Losey, L. (Dept. of Space Studies, Univ. of North Dakota, Grand Forks, ND (United States))

2011-07-15

This paper examines available data, develops a strategy and presents a monthly, global time series of fossil-fuel carbon dioxide emissions for the years 1950-2006. This monthly time series was constructed from detailed study of monthly data from the 21 countries that account for approximately 80% of global total emissions. These data were then used in a Monte Carlo approach to proxy for all remaining countries. The proportional-proxy methodology estimates by fuel group the fraction of annual emissions emitted in each country and month. Emissions from solid, liquid and gas fuels are explicitly modelled by the proportional-proxy method. The primary conclusion from this study is the global monthly time series is statistically significantly different from a uniform distribution throughout the year. Uncertainty analysis of the data presented show that the proportional-proxy method used faithfully reproduces monthly patterns in the data and the global monthly pattern of emissions is relatively insensitive to the exact proxy assignments used. The data and results presented here should lead to a better understanding of global and regional carbon cycles, especially when the mass data are combined with the stable carbon isotope data in atmospheric transport models

13C trend in an Egyptian recent tree as a record for global carbon dioxide behaviour

International Nuclear Information System (INIS)

Aly, A.I.M.; Belacy, N.; Abou El-Nour, F.

1988-01-01

The record of the 13 C content in tree rings of an Egyptian tree is used as indication for the increase of the atmospheric carbon dioxide concentration. A decrease of the 13 C isotopic content of the tree rings is observed starting from 1940 coinciding with a significant increase in the global production of CO 2 due to combustion of fossil fuel depleted in 13 C with respect to the atmosphere. Considering the local as well as the global CO 2 production rates together with the measured isotopic data, it may be concluded that the behaviour of carbon dioxide in the investigated Eastern Delta province in Egypt reflects mainly a global rather than a local effect. (author)

South African carbon observations: CO2 measurements for land, atmosphere and ocean

CSIR Research Space (South Africa)

Feig, Gregor T

2017-11-01

Full Text Available , Mudau AE, Monteiro PMS. South African carbon observations: CO2 measurements for land, atmosphere and ocean. S Afr J Sci. 2017;113(11/12), Art. #a0237, 4 pages. http://dx.doi. org/10.17159/sajs.2017/a0237 Carbon dioxide plays a central role in earth... References 1. Houghton RA. Balancing the global carbon budget. Annu Rev Earth Planet Sci. 2007;35:313–347. https://doi.org/10.1146/annurev. earth.35.031306.140057 2. Denman KL. Climate change, ocean processes and ocean iron fertilization. Mar Ecol Prog Ser...

Carbonic Anhydrase: An Efficient Enzyme with Possible Global Implications

Directory of Open Access Journals (Sweden)

Christopher D. Boone

2013-01-01

Full Text Available As the global atmospheric emissions of carbon dioxide (CO2 and other greenhouse gases continue to grow to record-setting levels, so do the demands for an efficient and inexpensive carbon sequestration system. Concurrently, the first-world dependence on crude oil and natural gas provokes concerns for long-term availability and emphasizes the need for alternative fuel sources. At the forefront of both of these research areas are a family of enzymes known as the carbonic anhydrases (CAs, which reversibly catalyze the hydration of CO2 into bicarbonate. CAs are among the fastest enzymes known, which have a maximum catalytic efficiency approaching the diffusion limit of 108 M−1s−1. As such, CAs are being utilized in various industrial and research settings to help lower CO2 atmospheric emissions and promote biofuel production. This review will highlight some of the recent accomplishments in these areas along with a discussion on their current limitations.

Role of volcanic forcing on future global carbon cycle

Directory of Open Access Journals (Sweden)

J. F. Tjiputra

2011-06-01

Full Text Available Using a fully coupled global climate-carbon cycle model, we assess the potential role of volcanic eruptions on future projection of climate change and its associated carbon cycle feedback. The volcanic-like forcings are applied together with a business-as-usual IPCC-A2 carbon emissions scenario. We show that very large volcanic eruptions similar to Tambora lead to short-term substantial global cooling. However, over a long period, smaller eruptions similar to Pinatubo in amplitude, but set to occur frequently, would have a stronger impact on future climate change. In a scenario where the volcanic external forcings are prescribed with a five-year frequency, the induced cooling immediately lower the global temperature by more than one degree before it returns to the warming trend. Therefore, the climate change is approximately delayed by several decades, and by the end of the 21st century, the warming is still below two degrees when compared to the present day period. Our climate-carbon feedback analysis shows that future volcanic eruptions induce positive feedbacks (i.e., more carbon sink on both the terrestrial and oceanic carbon cycle. The feedback signal on the ocean is consistently smaller than the terrestrial counterpart and the feedback strength is proportionally related to the frequency of the volcanic eruption events. The cooler climate reduces the terrestrial heterotrophic respiration in the northern high latitude and increases net primary production in the tropics, which contributes to more than 45 % increase in accumulated carbon uptake over land. The increased solubility of CO₂ gas in seawater associated with cooler SST is offset by a reduced CO₂ partial pressure gradient between the ocean and the atmosphere, which results in small changes in net ocean carbon uptake. Similarly, there is nearly no change in the seawater buffer capacity simulated between the different volcanic scenarios. Our study shows that even

Seagrass meadows as a globally significant carbonate reservoir

KAUST Repository

Mazarrasa, I.; Marbà , N.; Lovelock, C. E.; Serrano, O.; Lavery, P. S.; Fourqurean, J. W.; Kennedy, H.; Mateo, M. A.; Krause-Jensen, D.; Steven, A. D. L.; Duarte, Carlos M.

2015-01-01

There has been growing interest in quantifying the capacity of seagrass ecosystems to act as carbon sinks as a natural way of offsetting anthropogenic carbon emissions to the atmosphere. However, most of the efforts have focused on the particulate organic carbon (POC) stocks and accumulation rates and ignored the particulate inorganic carbon (PIC) fraction, despite important carbonate pools associated with calcifying organisms inhabiting the meadows, such as epiphytes and benthic invertebrates, and despite the relevance that carbonate precipitation and dissolution processes have in the global carbon cycle. This study offers the first assessment of the global PIC stocks in seagrass sediments using a synthesis of published and unpublished data on sediment carbonate concentration from 403 vegetated and 34 adjacent un-vegetated sites. PIC stocks in the top 1 m of sediment ranged between 3 and 1660 Mg PIC ha⁻¹, with an average of 654 ± 24 Mg PIC ha⁻¹, exceeding those of POC reported in previous studies by about a factor of 5. Sedimentary carbonate stocks varied across seagrass communities, with meadows dominated by Halodule, Thalassia or Cymodocea supporting the highest PIC stocks, and tended to decrease polewards at a rate of −8 ± 2 Mg PIC ha⁻¹ per degree of latitude (general linear model, GLM; p < 0.0003). Using PIC concentrations and estimates of sediment accretion in seagrass meadows, the mean PIC accumulation rate in seagrass sediments is found to be 126.3 ± 31.05 g PIC m⁻² yr⁻¹. Based on the global extent of seagrass meadows (177 000 to 600 000 km²), these ecosystems globally store between 11 and 39 Pg of PIC in the top metre of sediment and accumulate between 22 and 75 Tg PIC yr⁻¹, representing a significant contribution to the carbonate dynamics of coastal areas. Despite the fact that these high rates of carbonate accumulation imply CO₂

Seagrass meadows as a globally significant carbonate reservoir

KAUST Repository

Mazarrasa, I.

2015-08-24

There has been growing interest in quantifying the capacity of seagrass ecosystems to act as carbon sinks as a natural way of offsetting anthropogenic carbon emissions to the atmosphere. However, most of the efforts have focused on the particulate organic carbon (POC) stocks and accumulation rates and ignored the particulate inorganic carbon (PIC) fraction, despite important carbonate pools associated with calcifying organisms inhabiting the meadows, such as epiphytes and benthic invertebrates, and despite the relevance that carbonate precipitation and dissolution processes have in the global carbon cycle. This study offers the first assessment of the global PIC stocks in seagrass sediments using a synthesis of published and unpublished data on sediment carbonate concentration from 403 vegetated and 34 adjacent un-vegetated sites. PIC stocks in the top 1 m of sediment ranged between 3 and 1660 Mg PIC ha⁻¹, with an average of 654 ± 24 Mg PIC ha⁻¹, exceeding those of POC reported in previous studies by about a factor of 5. Sedimentary carbonate stocks varied across seagrass communities, with meadows dominated by Halodule, Thalassia or Cymodocea supporting the highest PIC stocks, and tended to decrease polewards at a rate of −8 ± 2 Mg PIC ha⁻¹ per degree of latitude (general linear model, GLM; p < 0.0003). Using PIC concentrations and estimates of sediment accretion in seagrass meadows, the mean PIC accumulation rate in seagrass sediments is found to be 126.3 ± 31.05 g PIC m⁻² yr⁻¹. Based on the global extent of seagrass meadows (177 000 to 600 000 km²), these ecosystems globally store between 11 and 39 Pg of PIC in the top metre of sediment and accumulate between 22 and 75 Tg PIC yr⁻¹, representing a significant contribution to the carbonate dynamics of coastal areas. Despite the fact that these high rates of carbonate accumulation imply CO₂

Bacteria in the greenhouse: Modeling the role of oceanic plankton in the global carbon cycle

International Nuclear Information System (INIS)

Ducklow, H.W.; Fasham, M.J.R.

1992-01-01

To plan effectively to deal with the greenhouse effect, a fundamental understanding is needed of the biogeochemical and physical machinery that cycles carbon in the global system; in addition, models are needed of the carbon cycle to project the effects of increasing carbon dioxide. In this chapter, a description is given of efforts to simulate the cycling of carbon and nitrogen in the upper ocean, concentrating on the model's treatment of marine phytoplankton, and what it reveals of their role in the biogeochemical cycling of carbon between the ocean and atmosphere. The focus is on the upper ocean because oceanic uptake appears to regulate the level of carbon dioxide in the atmosphere

Atmospheric methane from organic carbon mobilization in sedimentary basins — The sleeping giant?

Science.gov (United States)

Kroeger, K. F.; di Primio, R.; Horsfield, B.

2011-08-01

The mass of organic carbon in sedimentary basins amounts to a staggering 10 16 t, dwarfing the mass contained in coal, oil, gas and all living systems by ten thousand-fold. The evolution of this giant mass during subsidence and uplift, via chemical, physical and biological processes, not only controls fossil energy resource occurrence worldwide, but also has the capacity for driving global climate: only a tiny change in the degree of leakage, particularly if focused through the hydrate cycle, can result in globally significant greenhouse gas emissions. To date, neither climate models nor atmospheric CO 2 budget estimates have quantitatively included methane from thermal or microbial cracking of sedimentary organic matter deep in sedimentary basins. Recent estimates of average low latitude Eocene surface temperatures beyond 30 °C require extreme levels of atmospheric CO 2. Methane degassing from sedimentary basins may be a mechanism to explain increases of atmospheric CO 2 to values as much as 20 times higher than pre-industrial values. Increased natural gas emission could have been set in motion either by global tectonic processes such as pulses of activity in the global alpine fold belt, leading to increased basin subsidence and maturation rates in the prolific Jurassic and Cretaceous organic-rich sediments, or by increased magmatic activity such as observed in the northern Atlantic around the Paleocene-Eocene boundary. Increased natural gas emission would have led to global warming that was accentuated by long lasting positive feedback effects through temperature transfer from the surface into sedimentary basins. Massive gas hydrate dissociation may have been an additional positive feedback factor during hyperthermals superimposed on long term warming, such as the Paleocene-Eocene Thermal Maximum (PETM). As geologic sources may have contributed over one third of global atmospheric methane in pre-industrial time, variability in methane flux from sedimentary

Development of a low cost unmanned aircraft system for atmospheric carbon dioxide leak detection

Science.gov (United States)

Mitchell, Taylor Austin

Carbon sequestration, the storage of carbon dioxide gas underground, has the potential to reduce global warming by removing a greenhouse gas from the atmosphere. These storage sites, however, must first be monitored to detect if carbon dioxide is leaking back out to the atmosphere. As an alternative to traditional large ground-based sensor networks to monitor CO2 levels for leaks, unmanned aircraft offer the potential to perform in-situ atmospheric leak detection over large areas for a fraction of the cost. This project developed a proof-of-concept sensor system to map relative carbon dioxide levels to detect potential leaks. The sensor system included a Sensair K-30 FR CO2 sensor, GPS, and altimeter connected an Arduino microcontroller which logged data to an onboard SD card. Ground tests were performed to verify and calibrate the system including wind tunnel tests to determine the optimal configuration of the system for the quickest response time (4-8 seconds based upon flowrate). Tests were then conducted over a controlled release of CO 2 in addition to over controlled rangeland fires which released carbon dioxide over a large area as would be expected from a carbon sequestration source. 3D maps of carbon dioxide were developed from the system telemetry that clearly illustrated increased CO2 levels from the fires. These tests demonstrated the system's ability to detect increased carbon dioxide concentrations in the atmosphere.

The carbon-sequestration potential of a global afforestation program

International Nuclear Information System (INIS)

Nilsson, S.; Schopfhauser, W.

1995-01-01

The authors analyzed the changes in the carbon cycle that could be achieved with a global large-scale afforestation program that is economically, politically and technically feasible. They estimated that of the areas regarded as suitable for large-scale plantations, only about 345 million ha would actually be available for plantations and agroforestry for the sole purpose of sequestering carbon. The maximum annual rate of carbon fixation (1.48 Gt/yr) would only be achieved 60 years after the establishment of the plantation - 1.14 Gt by above-ground biomass and 0.34 Gt by below-ground biomass. Over the periods from 1995 to 2095, a total of 104 Gt of carbon would be sequestered. This is substantially lower than the amount of carbon required to offset current carbon emissions (3.8 Gt/yr) in order to stabilize the carbon content of the atmosphere. 108 refs., 1 fig., 14 tabs

Atmospheric methane: Sources, sinks, and role in global change

International Nuclear Information System (INIS)

Khalil, M.A.K.

1993-01-01

Atmospheric methane is thought to be the most important trace gas involved in man-made climate change. It may be second only to carbon dioxide in causing global warming. Methane affects also the oxidizing capacity of the atmosphere by controlling tropospheric OH radicals and creating O 3 , and it affects the ozone layer in the stratosphere by contributing water vapor and removing chlorine atoms. In the long term, methane is a natural product of life on earth, reaching high concentrations during warm and biologically productive epochs. Yet the scientific understanding of atmospheric methane has evolved mostly during the past decade after it was shown that concentrations were rapidly rising. Because of the environmental importance of methane, North Atlantic Treaty Organization's Scientific and Environmental Affairs Division commissioned an Advanced Research Workshop. This book is the result of such a conference held during the week of 6 October 1991 at Timberline Lodge on Mount Hood near Portland, Oregon. (orig./KW)

State of the Carbon Cycle - Consequences of Rising Atmospheric CO2

Science.gov (United States)

Moore, D. J.; Cooley, S. R.; Alin, S. R.; Brown, M. E.; Butman, D. E.; French, N. H. F.; Johnson, Z. I.; Keppel-Aleks, G.; Lohrenz, S. E.; Ocko, I.; Shadwick, E. H.; Sutton, A. J.; Potter, C. S.; Yu, R. M. S.

2016-12-01

The rise of atmospheric CO2, largely attributable to human activity through fossil fuel emissions and land-use change, has been dampened by carbon uptake by the ocean and terrestrial biosphere. We outline the consequences of this carbon uptake as direct and indirect effects on terrestrial and oceanic systems and processes for different regions of North America and the globe. We assess the capacity of these systems to continue to act as carbon sinks. Rising CO2 has decreased seawater pH; this process of ocean acidification has impacted some marine species and altered fundamental ecosystem processes with further effects likely. In terrestrial ecosystems, increased atmospheric CO2 causes enhanced photosynthesis, net primary production, and increased water-use efficiency. Rising CO2 may change vegetation composition and carbon storage, and widespread increases in water use efficiency likely influence terrestrial hydrology and biogeochemical cycling. Consequences for human populations include changes to ecosystem services including cultural activities surrounding land use, agricultural or harvesting practices. Commercial fish stocks have been impacted and crop production yields have been changed as a result of rising CO2. Ocean and terrestrial effects are contingent on, and feedback to, global climate change. Warming and modified precipitation regimes impact a variety of ecosystem processes, and the combination of climate change and rising CO2 contributes considerable uncertainty to forecasting carbon sink capacity in the ocean and on land. Disturbance regime (fire and insects) are modified with increased temperatures. Fire frequency and intensity increase, and insect lifecycles are disrupted as temperatures move out of historical norms. Changes in disturbance patterns modulate the effects of rising CO2 depending on ecosystem type, disturbance frequency, and magnitude of events. We discuss management strategies designed to limit the rise of atmospheric CO2 and reduce

State of the Carbon Cycle - Consequences of Rising Atmospheric CO2

Science.gov (United States)

Moore, David J.; Cooley, Sarah R.; Alin, Simone R.; Brown, Molly; Butman, David E.; French, Nancy H. F.; Johnson, Zackary I.; Keppel-Aleks; Lohrenz, Steven E.; Ocko, Ilissa;

Estimation of Global 1km-grid Terrestrial Carbon Exchange Part II: Evaluations and Applications

Science.gov (United States)

Murakami, K.; Sasai, T.; Kato, S.; Niwa, Y.; Saito, M.; Takagi, H.; Matsunaga, T.; Hiraki, K.; Maksyutov, S. S.; Yokota, T.

2015-12-01

Global terrestrial carbon cycle largely depends on a spatial pattern in land cover type, which is heterogeneously-distributed over regional and global scales. Many studies have been trying to reveal distribution of carbon exchanges between terrestrial ecosystems and atmosphere for understanding global carbon cycle dynamics by using terrestrial biosphere models, satellite data, inventory data, and so on. However, most studies remained within several tens of kilometers grid spatial resolution, and the results have not been enough to understand the detailed pattern of carbon exchanges based on ecological community and to evaluate the carbon stocks by forest ecosystems in each countries. Improving the sophistication of spatial resolution is obviously necessary to enhance the accuracy of carbon exchanges. Moreover, the improvement may contribute to global warming awareness, policy makers and other social activities. We show global terrestrial carbon exchanges (net ecosystem production, net primary production, and gross primary production) with 1km-grid resolution. The methodology for these estimations are shown in the 2015 AGU FM poster "Estimation of Global 1km-grid Terrestrial Carbon Exchange Part I: Developing Inputs and Modelling". In this study, we evaluated the carbon exchanges in various regions with other approaches. We used the satellite-driven biosphere model (BEAMS) as our estimations, GOSAT L4A CO2 flux data, NEP retrieved by NICAM and CarbonTracer2013 flux data, for period from Jun 2001 to Dec 2012. The temporal patterns for this period were indicated similar trends between BEAMS, GOSAT, NICAM, and CT2013 in many sub-continental regions. Then, we estimated the terrestrial carbon exchanges in each countries, and could indicated the temporal patterns of the exchanges in large carbon stock regions.Global terrestrial carbon cycle largely depends on a spatial pattern of land cover type, which is heterogeneously-distributed over regional and global scales. Many

Forecasting global atmospheric CO2

International Nuclear Information System (INIS)

Agusti-Panareda, A.; Massart, S.; Boussetta, S.; Balsamo, G.; Beljaars, A.; Engelen, R.; Jones, L.; Peuch, V.H.; Chevallier, F.; Ciais, P.; Paris, J.D.; Sherlock, V.

2014-01-01

A new global atmospheric carbon dioxide (CO 2 ) real-time forecast is now available as part of the preoperational Monitoring of Atmospheric Composition and Climate - Interim Implementation (MACC-II) service using the infrastructure of the European Centre for Medium-Range Weather Forecasts (ECMWF) Integrated Forecasting System (IFS). One of the strengths of the CO 2 forecasting system is that the land surface, including vegetation CO 2 fluxes, is modelled online within the IFS. Other CO 2 fluxes are prescribed from inventories and from off-line statistical and physical models. The CO 2 forecast also benefits from the transport modelling from a state-of-the-art numerical weather prediction (NWP) system initialized daily with a wealth of meteorological observations. This paper describes the capability of the forecast in modelling the variability of CO 2 on different temporal and spatial scales compared to observations. The modulation of the amplitude of the CO 2 diurnal cycle by near-surface winds and boundary layer height is generally well represented in the forecast. The CO 2 forecast also has high skill in simulating day-to-day synoptic variability. In the atmospheric boundary layer, this skill is significantly enhanced by modelling the day-to-day variability of the CO 2 fluxes from vegetation compared to using equivalent monthly mean fluxes with a diurnal cycle. However, biases in the modelled CO 2 fluxes also lead to accumulating errors in the CO 2 forecast. These biases vary with season with an underestimation of the amplitude of the seasonal cycle both for the CO 2 fluxes compared to total optimized fluxes and the atmospheric CO 2 compared to observations. The largest biases in the atmospheric CO 2 forecast are found in spring, corresponding to the onset of the growing season in the Northern Hemisphere. In the future, the forecast will be re-initialized regularly with atmospheric CO 2 analyses based on the assimilation of CO 2 products retrieved from satellite

1km Global Terrestrial Carbon Flux: Estimations and Evaluations

Science.gov (United States)

Murakami, K.; Sasai, T.; Kato, S.; Saito, M.; Matsunaga, T.; Hiraki, K.; Maksyutov, S. S.

2017-12-01

Estimating global scale of the terrestrial carbon flux change with high accuracy and high resolution is important to understand global environmental changes. Furthermore the estimations of the global spatiotemporal distribution may contribute to the political and social activities such as REDD+. In order to reveal the current state of terrestrial carbon fluxes covering all over the world and a decadal scale. The satellite-based diagnostic biosphere model is suitable for achieving this purpose owing to observing on the present global land surface condition uniformly at some time interval. In this study, we estimated the global terrestrial carbon fluxes with 1km grids by using the terrestrial biosphere model (BEAMS). And we evaluated our new carbon flux estimations on various spatial scales and showed the transition of forest carbon stocks in some regions. Because BEAMS required high resolution meteorological data and satellite data as input data, we made 1km interpolated data using a kriging method. The data used in this study were JRA-55, GPCP, GOSAT L4B atmospheric CO2 data as meteorological data, and MODIS land product as land surface satellite data. Interpolating process was performed on the meteorological data because of insufficient resolution, but not on MODIS data. We evaluated our new carbon flux estimations using the flux tower measurement (FLUXNET2015 Datasets) in a point scale. We used 166 sites data for evaluating our model results. These flux sites are classified following vegetation type (DBF, EBF, ENF, mixed forests, grass lands, croplands, shrub lands, Savannas, wetlands). In global scale, the BEAMS estimations was underestimated compared to the flux measurements in the case of carbon uptake and release. The monthly variations of NEP showed relatively high correlations in DBF and mixed forests, but the correlation coefficients of EBF, ENF, and grass lands were less than 0.5. In the meteorological factors, air temperature and solar radiation showed

The global carbon cycle change: Le Chatelier principle in the response of biota to changing CO2 concentration in the atmosphere

International Nuclear Information System (INIS)

Gorshkov, V.G.; Sherman, S.G.; Kondratyev, K.Y.

1990-01-01

The long-term existence of natural biota in the environment means that such a system is stable with respect to external disturbances. This system must follow the Le Chatelier principle which is based on the processes that compensate the disturbing effects. The use of the Le Chatelier principle makes it possible to choose between contradictory observational data. Available observational data on variations of the concentration of rare carbon isotopes in various media show that the oceanic biota follows the Le Chatelier principle and absorbs about half the carbon which the ocean gets from the atmosphere, compensating an increment of carbon in the atmosphere caused by an anthropogenic impact. The strongly anthropogenetically disturbed land biota does not follow the Le Chatelier principle, starting from the middle of this century. The land biota not only cannot absorb excess carbon accumulated in the atmosphere: it ejects carbon to the atmosphere in quantities equal to halved emission of carbon through fossil fuel burning. All the quantitative results considered in this paper have been obtained without using models of the biota and of the ocean

High Resolution Spectra of Carbon Monoxide, Propane and Ammonia for Atmospheric Remote Sensing

Science.gov (United States)

Beale, Christopher Andrew

Experiment satellite of carbon monoxide. The effect of the atmosphere's chemistry and physics on this molecule is measured through its isotopologues, primarily 13CO (carbon-13 substituted carbon monoxide). Isotopic chemistry allows a key analysis of the atmosphere as it may be used as a tracer for chemical reactions and dynamical processes. The carbon monoxide fractionation results in Chapter IV present the first global measurements of isotopic fractionation of CO, showing significant fractionation in the upper atmosphere (60-80 km) as a result of the photolysis of carbon dioxide (CO2).

The Century-Long Challenge of Global Carbon Management

Science.gov (United States)

Socolow, R.

2002-05-01

The time scale of the global carbon management is a century, not a decade and not a millennium. A century is the ratio of 1000 billion metric tons of carbon [Gt(C)] to 10 Gt(C)/yr. 1000 Gt(C) is the future emissions that will lead to approximately a doubling of the pre-industrial atmospheric CO2 concentration, 280 ppm, assuming the total net ocean plus terrestrial sink remains at half the strength of this source - since 2.1 Gt (C) = 1 ppm, and the concentration today is already 370 ppm. Doubling is the most widely used boundary between acceptable and unacceptable Greenhouse-related environmental disruption, or, in the language of the Framework Convention on Climate Change, the onset of "dangerous anthropogenic interference with the climate system." And 10 Gt(C)/yr is a conservative estimate of the average annual fossil-fuel carbon source over the century; it is now between 6 and 7 Gt(C). Conventional oil and gas are not sufficiently abundant to generate a serious Greenhouse problem on their own. Well before their cumulative carbon emissions reach 1000 Gt(C), both are expected to become non-competitive as a result of growing costs of access (costs related to resources being very deep underground, or below very deep water, or very remote, or very small.) But several times 1000 Gt(C) of coal resources will probably be competitive with non-fossil fuel alternatives, as will "unconventional" oil and gas resources, such as tar sands. The world will not be saved from a serious Greenhouse problem by fossil fuel depletion. There are four mitigation strategies for avoiding dangerous interference with the climate system. Fossil fuels can cease to dominate the global energy system well before the end of the century, yielding large market share to some combination of renewable energy and nuclear (fission and fusion) energy sources. Fossil fuels can continue to dominate, but most of the carbon in the century's fossil fuels can be prevented from reaching the atmosphere (fossil-carbon

Quantification of the "global" authigenic carbonate δ13C value and implications for carbon cycling

Science.gov (United States)

Loyd, S. J.

2017-12-01

Relationships among early Earth ocean chemistry, atmospheric chemistry and the evolution/radiation of life have been inferred from carbon isotope compositions (δ13C) of marine carbonates. Under steady-state conditions, the isotope compositions of marine carbonates reflect both the amount and δ13C of carbon entering and leaving the oceans. Recently the traditional "two-output" (marine carbonate and organic matter) mass-balance equation has been modified to include a third, authigenic carbonate output term. However, the formation mechanisms of authigenic carbonates remain poorly understood, particularly from a global prospective. The utility of the new mass-balance approach will be limited until authigenic carbonates are better characterized (e.g., through δ13C analyses). Authigenic carbonates form largely as a result of 1) the respiratory degradation of organic matter (e.g., sulfate reduction), 2) the oxidation of methane and 3) the production of methane. These major reaction pathways can produce authigenic carbonates with highly variable δ13C compositions (δ13Cac). Spatiotemporal variation in the extent and prevalence of different pathways therefore exert a first order control on "global" δ13Cac. Here, values are compiled from new and existing data sets and a modern, global δ13Cac is calculated. When calculated as an average of all data or an averaged mean of individual sites, this value is very similar to normal marine sedimentary organic matter. This finding suggests that marine sediments behave largely as closed systems in the context of organic matter degradation and carbonate authigenesis. In addition, the lack of significant difference between authigenic and organic δ13C implies that these two mass-balance output terms can be considered collectively in more recent time intervals. It may be appropriate to separate these two terms when characterizing more ancient settings when redox characteristics promoted more reducing organic matter degradation

Assessment of pre-industrial carbon dioxide content in the atmosphere using hydro-chemical data

International Nuclear Information System (INIS)

Heans, K.A.; Liaxin, Y.I.

2001-01-01

A hydrochemical method has been developed to calculate concentrations of carbon dioxide (CO 2 ) in the pre-industrial atmosphere and its relationship to climatic change. The following factors affect the Earth's climate: (1) the sun with all its processes, (2) the attraction of the moon that limits the axis of inclination of the Earth, and (3) the cycle of carbon dioxide and the greenhouse effect. An imbalance in the climate system would be a major global disaster that could be detrimental for life on Earth. Recent studies and temperature measurements have shown a trend in which air temperature has increased in the troposphere in the last 100 years, affecting the normal development of natural processes. Various phenomena result from climatic change, or the gradual heating of the Earth. These include the weakening of the glacial layer that covers the Earth's surface, cycles of prolonged slowing in freeze and thaw periods of aquatic surfaces, and increased air temperature in the troposphere which can also causes abnormal fluctuations of temperature in the atmosphere, resulting in heat waves and droughts. Gradual heating of the Earth can also result in rainy periods that produce devastating floods, hurricanes and extreme winds. Changes in water temperature can influence pH levels which affect certain marine species. An increase of 5 degrees C in the global average atmospheric temperature has created changes in 420 physical processes as well as in the behavior of plants and animals. The author stated that the most drastic factor that affects the balance of the Earth's climate is the actions of man interfering with the carbon cycle, as carbon dioxide plays a vital role in the formation of the greenhouse effect. The problem results from an imbalance of the carbon dioxide cycle when CO 2 emissions are increased through the combustion of fossil fuels. It was determined that before the beginning of the Industrial Revolution, carbon dioxide in the atmosphere was 256 ppm

The contribution of weathering of the main Alpine rivers on the global carbon cycle

Science.gov (United States)

Donnini, Marco; Probst, Jean-Luc; Probst, Anne; Frondini, Francesco; Marchesini, Ivan; Guzzetti, Fausto

2013-04-01

classification of Meybeck (1986, 1987). Then for each basin we computed Rsil weighted average considering the surface and the mean precipitation for the surface area of each lithology. Lastly, we estimated the (Ca+Mg) originating from carbonate weathering as the remaining cations after silicate correction. Depending on time-scales of the phenomena (shorter than about 1 million year i.e., correlated to the short term carbon cycle, or longer than about 1 million years i.e., correlated to the long-term carbon cycle), we considered different equations for the quantification of the atmospheric CO2 consumed by weathering (Huh, 2010). The results show the net predominance of carbonate weathering on fixing atmospheric CO2 and that, considering the long-term carbon cycle, the amount of atmospheric CO2 uptake by weathering is about one order of magnitude lower than considering the short-term carbon cycle. Moreover, considering the short-term carbon cycle, the mean CO2 consumed by Alpine basins is of the same order of magnitude of the mean CO2 consumed by weathering by the 60 largest rivers of the world estimated by Gaillardet et al. (1999). References Amiotte-Suchet, P. "Cycle Du Carbone, Érosion Chimique Des Continents Et Transfert Vers Les Océans." Sci. Géol. Mém. Strasbourg 97 (1995): 156. Amiotte-Suchet, P., and J.-L. Probst. "Origins of dissolved inorganic carbon in the Garonne river waters: seasonal and interannual variations." Sci. Géologiques Bull. Strasbourg 49, no. 1-4 (1996): 101-126. Berner, E.K., and R.A. Berner. The Global Water Cycle. Geochemistry and Environment. Prentice Halle. Engelwood Cliffs, NJ, 1987. Drever, J.L. The Geochemistry of Natural Waters. Prentice Hall, 1982. Gaillardet, J., B. Dupré, P. Louvat, and C.J. Allègre. "Global Silicate Weathering and CO2 Consumption Rates Deduced from the Chemistry of Large Rivers." Chemical Geology 159 (1999): 3-30. Garrels, R.M., and F.T. Mackenzie. Evolution of Sedimentary Rocks. New York: W.W. Nortonand, 1971. Huh, Y

Evaluation and intercomparison of three-dimensional global marine carbon cycle models

Energy Technology Data Exchange (ETDEWEB)

Caldeira, K., LLNL

1998-07-01

The addition of carbon dioxide to the atmosphere from fossil fuel burning and deforestation has profound implications for the future of the earth`s climate and hence for humankind itself. Society is looking toward the community of environmental scientists to predict the consequences of increased atmospheric carbon dioxide so that sound input can be provided to economists, environmental engineers, and, ultimately, policy makers. Environmental scientists have responded to this challenge through the creation of several ambitious, highly-coordinated programs, each focused on a different aspect of the climate system. Recognizing that numerical models, be they relatively simple statistical-empirical models or highly complex process-oriented models, are the only means for predicting the future of the climate system, all of these programs include the development of accurate, predictive models as a central goal. The Joint Global Ocean Flux Study (JGOFS) is one such program, and was built on the well-founded premise that biological, chemical and physical oceanographic processes have a profound influence on the C0{sub 2} content of the atmosphere. The, cap-stone, phase of JGOFS, the Synthesis and Modeling Project (SMP), is charged with the development of models that can be used in the prediction of future air-sea partitioning of C0{sub 2}. JGOFS, particularly the SMP phase, has a number of interim goals as well, including the determination of fluxes and inventories of carbon in the modern ocean that air germane to the air-sea partitioning of C0{sub 2}. Models have a role to play here too, because many of these fluxes and inventories, such as the distributions of anthropogenic dissolved inorganic carbon (DIC), new primary production and aphotic zone remineralization, while not amenable to direct observation on the large scale, can be determined using a variety of modeling approaches (Siegenthaler and Oeschger, 1987; Maier-Reimer and Hasselman, 1987, Bacastow and Maier

The mid-Cretaceous super plume, carbon dioxide, and global warming

Science.gov (United States)

Caldeira, Ken; Rampino, Michael R.

1991-01-01

Carbon-dioxide releases associated with a mid-Cretaceous super plume and the emplacement of the Ontong-Java Plateau have been suggested as a principal cause of the mid-Cretaceous global warming. A carbonate-silicate cycle model is developed to quantify the possible climatic effects of these CO2 releases, utilizing four different formulations for the rate of silicate-rock weathering as a function of atmospheric CO2. CO2 emissions resulting from super-plume tectonics could have produced atmospheric CO2 levels from 3.7 to 14.7 times the modern preindustrial value of 285 ppm. Based on the temperature sensitivity to CO2 increases used in the weathering-rate formulations, this would cause a global warming of from 2.8 to 7.7 C over today's glogal mean temperature. Altered continental positions and higher sea level may have been contributed about 4.8 C to mid-Cretaceous warming. Thus, the combined effects of paleogeographic changes and super-plume related CO2 emissions could be in the range of 7.6 to 12.5 C, within the 6 to 14 C range previously estimated for mid-Cretaceous warming. CO2 releases from oceanic plateaus alone are unlikely to have been directly responsible for more than 20 percent of the mid-Cretaceous increase in atmospheric CO2.

The Global Land-Ocean Temperature Index in Relation to Sunspot Number, the Atlantic Multidecadal Oscillation Index, the Mauna Loa Atmospheric Concentration of CO2, and Anthropogenic Carbon Emissions

Science.gov (United States)

Wilson, Robert M.

2013-01-01

Global warming/climate change has been a subject of scientific interest since the early 19th century. In particular, increases in the atmospheric concentration of carbon dioxide (CO2) have long been thought to account for Earth's increased warming, although the lack of a dependable set of observational data was apparent as late as the mid 1950s. However, beginning in the late 1950s, being associated with the International Geophysical Year, the opportunity arose to begin accurate continuous monitoring of the Earth's atmospheric concentration of CO2. Consequently, it is now well established that the atmospheric concentration of CO2, while varying seasonally within any particular year, has steadily increased over time. Associated with this rising trend in the atmospheric concentration of CO2 is a rising trend in the surface-air and sea-surface temperatures (SSTs). This Technical Publication (TP) examines the statistical relationships between 10-year moving averages (10-yma) of the Global Land-Ocean Temperature Index (GLOTI), sunspot number (SSN), the Atlantic Multidecadal Oscillation (AMO) index, and the Mauna Loa CO2 (MLCO2) index for the common interval 1964-2006, where the 10-yma values are used to indicate trends in the data. Scatter plots using the 10-yma values between GLOTI and each of the other parameters are determined, both as single-variate and multivariate fits. Scatter plots are also determined for MLCO2 using single-variate and bivariate (BV) fits, based on the GLOTI alone and the GLOTI in combination with the AMO index. On the basis of the inferred preferential fits for MLCO2, estimates for MLCO2 are determined for the interval 1885-1964, thereby yielding an estimate of the preindustrial level of atmospheric concentration of CO2. Lastly, 10-yma values of MLCO2 are compared against 10-yma estimates of the total carbon emissions (TCE) to determine the likelihood that manmade sources of carbon emissions are indeed responsible for the recent warming now

The atmosphere: Global commons to protect

International Nuclear Information System (INIS)

Obasi, G.O.P.

1996-01-01

One of the most important greenhouse gases is CO 2 , whose concentration in the atmosphere has increased from 280 parts per million by volume (ppmv) to 358ppmv in 1994, giving a general increase of over 27 per cent since pre-industrial times. This increase has been attributed largely to fossil fuel combustion. Significant increases have also been observed in atmospheric concentrations of the other greenhouse gases, including methane, nitrous oxide and global tropospheric ozone. Concentrations of methane and nitrous oxide have, for example, grown by 145 per cent and 15 per cent respectively since pre-industrial times. Such increases have been linked to the rapid world population growth, which has resulted in increasing demands for energy, food, water, shelter and other basic needs. Computer models indicate that the continued accumulation of greenhouse gases in the atmosphere could result in global climate change and global warming. As some uncertainties still exists in the model predictions, it may take a few more years to uniquely separate human-induced climate change signals from natural climate variability in global climate trends

Acceleration of global warming due to carbon-cycle feedbacks in a coupled climate model

International Nuclear Information System (INIS)

Cox, P.M.; Betts, R.A.; Jones, C.D.; Spall, S.A.; Totterdell, I.J.

2000-01-01

The continued increase in the atmospheric concentration of carbon dioxide due to anthropogenic emissions is predicted to lead to significant changes in climate. About half of the current emissions are being absorbed by the ocean and by land ecosystems, but this absorption is sensitive to climate as well as to atmospheric carbon dioxide concentrations, creating a feedback loop. General circulation models have generally excluded the feedback between climate and the biosphere, using static vegetation distributions and CO 2 concentrations from simple carbon-cycle models that do not include climate change. Here we present results from a fully coupled, three-dimensional carbon-climate model, indicating that carbon-cycle feedbacks could significantly accelerate climate change over the twenty-first century. We find that under a 'business as usual' scenario, the terrestrial biosphere acts as an overall carbon sink until about 2050, but turns into a source thereafter. By 2100, the ocean uptake rate of 5 Gt C yr -1 is balanced by the terrestrial carbon source, and atmospheric CO 2 concentrations are 250 p.p.m.v. higher in our fully coupled simulation than in uncoupled carbon models, resulting in a global-mean warming of 5.5 K, as compared to 4 K without the carbon-cycle feedback. (author)

Assessment of Anthropogenic and Climatic Impacts on the Global Carbon Cycle Using a 3-D Model Constrained by Isotopic Carbon Measurements and Remote Sensing of Vegetation

Science.gov (United States)

Keeling, Charles D.; Piper, S. C.

1998-01-01

Our original proposal called for improved modeling of the terrestrial biospheric carbon cycle, specifically using biome-specific process models to account for both the energy and water budgets of plant growth, to facilitate investigations into recent changes in global atmospheric CO2 abundance and regional distribution. The carbon fluxes predicted by these models were to be incorporated into a global model of CO2 transport to establish large-scale regional fluxes of CO2 to and from the terrestrial biosphere subject to constraints imposed by direct measurements of atmospheric CO2 and its 13C/12C isotopic ratio. Our work was coordinated with a NASA project (NASA NAGW-3151) at the University of Montana under the direction of Steven Running, and was partially funded by the Electric Power Research Institute. The primary objective of this project was to develop and test the Biome-BGC model, a global biological process model with a daily time step which simulates the water, energy and carbon budgets of plant growth. The primary product, the unique global gridded daily land temperature, and the precipitation data set which was used to drive the process model is described. The Biome-BGC model was tested by comparison with a simpler biological model driven by satellite-derived (NDVI) Normalized Difference Vegetation Index and (PAR) Photosynthetically Active Radiation data and by comparison with atmospheric CO2 observations. The simple NDVI model is also described. To facilitate the comparison with atmospheric CO2 observations, a three-dimensional atmospheric transport model was used to produce predictions of atmospheric CO2 variations given CO2 fluxes owing to (NPP) Net Primary Productivity and heterotrophic respiration that were produced by the Biome-BGC model and by the NDVI model. The transport model that we used in this project, and errors associated with transport simulations, were characterized by a comparison of 12 transport models.

Global carbon - nitrogen - phosphorus cycle interactions: A key to solving the atmospheric CO2 balance problem?

Science.gov (United States)

Peterson, B. J.; Mellillo, J. M.

1984-01-01

If all biotic sinks of atmospheric CO2 reported were added a value of about 0.4 Gt C/yr would be found. For each category, a very high (non-conservative) estimate was used. This still does not provide a sufficient basis for achieving a balance between the sources and sinks of atmospheric CO2. The bulk of the discrepancy lies in a combination of errors in the major terms, the greatest being in a combination of errors in the major terms, the greatest being in the net biotic release and ocean uptake segments, but smaller errors or biases may exist in calculations of the rate of atmospheric CO2 increase and total fossil fuel use as well. The reason why biotic sinks are not capable of balancing the CO2 increase via nutrient-matching in the short-term is apparent from a comparison of the stoichiometry of the sources and sinks. The burning of fossil fuels and forest biomass releases much more CO2-carbon than is sequestered as organic carbon.

A framework for assessing global change risks to forest carbon stocks in the United States

Science.gov (United States)

Christopher W. Woodall; Grant M. Domke; Karin L. Riley; Christopher M. Oswalt; Susan J. Crocker; Gary W. Yohe

2013-01-01

Among terrestrial environments, forests are not only the largest long-term sink of atmospheric carbon (C), but are also susceptible to global change themselves, with potential consequences including alterations of C cycles and potential C emission. To inform global change risk assessment of forest C across large spatial/temporal scales, this study constructed and...

Fighting global warming by greenhouse gas removal: destroying atmospheric nitrous oxide thanks to synergies between two breakthrough technologies.

Science.gov (United States)

Ming, Tingzhen; de Richter, Renaud; Shen, Sheng; Caillol, Sylvain

2016-04-01

Even if humans stop discharging CO2 into the atmosphere, the average global temperature will still increase during this century. A lot of research has been devoted to prevent and reduce the amount of carbon dioxide (CO2) emissions in the atmosphere, in order to mitigate the effects of climate change. Carbon capture and sequestration (CCS) is one of the technologies that might help to limit emissions. In complement, direct CO2 removal from the atmosphere has been proposed after the emissions have occurred. But, the removal of all the excess anthropogenic atmospheric CO2 will not be enough, due to the fact that CO2 outgases from the ocean as its solubility is dependent of its atmospheric partial pressure. Bringing back the Earth average surface temperature to pre-industrial levels would require the removal of all previously emitted CO2. Thus, the atmospheric removal of other greenhouse gases is necessary. This article proposes a combination of disrupting techniques to transform nitrous oxide (N2O), the third most important greenhouse gas (GHG) in terms of current radiative forcing, which is harmful for the ozone layer and possesses quite high global warming potential. Although several scientific publications cite "greenhouse gas removal," to our knowledge, it is the first time innovative solutions are proposed to effectively remove N2O or other GHGs from the atmosphere other than CO2.

New method of radiation measurement at carbon isotope 14 low level in an environmental atmospheric sampling

International Nuclear Information System (INIS)

Tormos, J.

2009-01-01

A new method of preparation is proposed to extract the atmospheric carbon trapped in the solution of soda coming from air sampling in environment with a carbon-14 bubbler (type H.A.G. 7000). It is based on the neutralisation of the global soda solution got from bubbling pots by nitric acid, the complete desorption of the carbon under gaseous oxidized form (CO 2 ) and its trapping in a only capacity containing a reactive. The whole of the device is scanned by air at steady rate. A test catch of the reactive and of the trapped carbon dioxide is then blended to a glistening liquid (Permafluor E+) and measured in beta counting by scintillation in liquid medium with a counter for the measurement of low energy beta emitters at very low level of activity (Quantulus type). this method allows to get a limit of detection equal to 5 mBq/m 3 for the atmospheric organic carbon. The principal interest of this method is its quickness and simplicity of setting in motion for a measurement of 14 C in the atmospheric carbon dioxide at a level of natural activity. (N.C.)

'Carbon-Money Exchange' to contain global warming and deforestation

International Nuclear Information System (INIS)

Nagase, Kozo

2005-01-01

This paper builds a basic theory of 'Carbon-Money Exchange' in which carbon as currency in nature's household (ecosystems) and money as currency in humankind's household (economy) are exchanged just like in a foreign exchange. The simple chemical equation below makes it possible (CO 2 →C+O 2 =C+O 2 →CO 2 ). The left-hand side represents the work of plants to remove atmospheric CO 2 . The right-hand side represents the work of humans as fossil fuel consumers to produce it. The exchange of the two currencies is possible by copying the fossil fuel market. The paper concludes that this new exchange can automatically contain global warming and deforestation, replacing onerous emissions trading. Moreover, it could revolutionize the conventional economy, creating counter-capitalism, or 'carbonism'

Marine atmospheric corrosion of carbon steels

Energy Technology Data Exchange (ETDEWEB)

Morcillo, M.; Alcantara, J.; Diaz, I.; Chico, B.; Simancas, J.; Fuente, D. de la

2015-07-01

Basic research on marine atmospheric corrosion of carbon steels is a relatively young scientific field and there continue to be great gaps in this area of knowledge. The presence of akaganeite in the corrosion products that form on steel when it is exposed to marine atmospheres leads to a notable increase in the corrosion rate. This work addresses the following issues: (a) environmental conditions necessary for akaganeite formation; (b) characterisation of akaganeite in the corrosion products formed; (c) corrosion mechanisms of carbon steel in marine atmospheres; (d) exfoliation of rust layers formed in highly aggressive marine atmospheres; (e) long-term corrosion rate prediction; and (f) behaviour of weathering steels. Field research has been carried out at Cabo Vilano wind farm (Camarinas, Galicia) in a wide range of atmospheric salinities and laboratory work involving the use of conventional atmospheric corrosion techniques and near-surface and bulk sensitive analytical techniques: scanning electron microscopy (SEM)/energy dispersive spectrometry (EDS), X-ray diffraction (XRD), Mossbauer spectroscopy and SEM/μRaman spectroscopy. (Author)

Comparison of the Carbon System Parameters at the Global CO2 Survey Crossover Locations in the North and South Pacific Ocean, 1990-1996

Energy Technology Data Exchange (ETDEWEB)

Feely, Richard A [NOAA, Pacific Marine Environmental Laboratory (PMEL); Lamb, Marilyn F. [NOAA, Pacific Marine Environmental Laboratory (PMEL); Greeley, Dana J. [NOAA, Pacific Marine Environmental Laboratory (PMEL); Wanninkhof, Rik [NOAA, Atlantic Oceanographic and Meteorological Laboratory (AOML)

1999-10-01

As a collaborative program to measure global ocean carbon inventories and provide estimates of the anthropogenic carbon dioxide (C02) uptake by the oceans. the National Oceanic and Atmospheric Administration and the U.S. Department of Energy have sponsored the collection of ocean carbon measurements as part of the World Ocean Circulation Experiment and Ocean-Atmosphere Carbon Exchange Study cruises. The cruises discussed here occurred in the North and South Pacific from 1990 through 1996. The carbon parameters from these 30 crossover locations have been compared to ensure that a consistent global data set emerges from the survey cruises. !'he results indicate that for dissolved inorganic carbon. fugacity of C02• and pH. the a~:,rreements at most crossover locations are well within the design specifications for the global CO) survey: whereas. in the case of total alkaliniry. the agreement between crossover locations is not as close.

The global atmospheric environment for the next generation

NARCIS (Netherlands)

Dentener, F.; Stevenson, D.; Ellingsen, K.; Noije, van T.; Schultz, M.; Amann, M.; Atherton, C.; Bell, N.; Bergmann, D.; Bey, I.; Bouwman, L.; Butler, T.; Cofala, J.; Collins, B.; Drevet, J.; Doherty, R.; Eickhout, B.; Eskes, H.; Fiore, A.; Gauss, M.; Hauglustaine, D.; Horowitz, L.; Isaksen, I.S.A.; Josse, B.; Lawrence, M.; Krol, M.C.; Lamarque, J.F.; Montanaro, V.; Müller, J.F.; Peuch, V.H.; Pitari, G.; Pyle, J.; Rast, S.; Rodriguez, J.; Sanderson, M.; Savage, N.H.; Shindell, D.; Strahan, S.; Szopa, S.; Sudo, K.; Dingenen, van R.; Wild, O.; Zeng, G.

2006-01-01

Air quality, ecosystem exposure to nitrogen deposition, and climate change are intimately coupled problems: we assess changes in the global atmospheric environment between 2000 and 2030 using 26 state-of-the-art global atmospheric chemistry models and three different emissions scenarios. The first

Simulated effects of nitrogen saturation the global carbon budget using the IBIS model

Science.gov (United States)

Lu, Xuehe; Jiang, Hong; Liu, Jinxun; Zhang, Xiuying; Jin, Jiaxin; Zhu, Qiuan; Zhang, Zhen; Peng, Changhui

2016-01-01

Over the past 100 years, human activity has greatly changed the rate of atmospheric N (nitrogen) deposition in terrestrial ecosystems, resulting in N saturation in some regions of the world. The contribution of N saturation to the global carbon budget remains uncertain due to the complicated nature of C-N (carbon-nitrogen) interactions and diverse geography. Although N deposition is included in most terrestrial ecosystem models, the effect of N saturation is frequently overlooked. In this study, the IBIS (Integrated BIosphere Simulator) was used to simulate the global-scale effects of N saturation during the period 1961–2009. The results of this model indicate that N saturation reduced global NPP (Net Primary Productivity) and NEP (Net Ecosystem Productivity) by 0.26 and 0.03 Pg C yr−1, respectively. The negative effects of N saturation on carbon sequestration occurred primarily in temperate forests and grasslands. In response to elevated CO2 levels, global N turnover slowed due to increased biomass growth, resulting in a decline in soil mineral N. These changes in N cycling reduced the impact of N saturation on the global carbon budget. However, elevated N deposition in certain regions may further alter N saturation and C-N coupling.

Atmospheric Inversion of the Global Surface Carbon Flux with Consideration of the Spatial Distributions of US Crop Production and Consumption

Science.gov (United States)

Fung, Jonathan Winston

Carbon dioxide is taken up by crops during production and released back to the atmosphere at different geographical locations through respiration of consumed crop commodities. In this study, spatially distributed county-level US cropland net primary productivity, harvested biomass, changes in soil carbon, and human and livestock consumption data were integrated into the prior terrestrial biosphere flux generated by the Boreal Ecosystem Productivity Simulator (BEPS). A global time-dependent Bayesian synthesis inversion with a nested focus on North America was carried out based on CO2 observations at 210 stations. Overall, the inverted annual North American CO2 sink weakened by 6.5% over the period from 2002 to 2007 compared to simulations disregarding US crop statistical data. The US Midwest is found to be the major sink of 0.36±0.13 PgC yr-1 whereas the large sink in the US Southeast forests weakened to 0.16±0.12 PgC yr-1 partly due to local CO2 sources from crop consumption.

Estimation of Global 1km-grid Terrestrial Carbon Exchange Part I: Developing Inputs and Modelling

Science.gov (United States)

Sasai, T.; Murakami, K.; Kato, S.; Matsunaga, T.; Saigusa, N.; Hiraki, K.

2015-12-01

Global terrestrial carbon cycle largely depends on a spatial pattern in land cover type, which is heterogeneously-distributed over regional and global scales. However, most studies, which aimed at the estimation of carbon exchanges between ecosystem and atmosphere, remained within several tens of kilometers grid spatial resolution, and the results have not been enough to understand the detailed pattern of carbon exchanges based on ecological community. Improving the sophistication of spatial resolution is obviously necessary to enhance the accuracy of carbon exchanges. Moreover, the improvement may contribute to global warming awareness, policy makers and other social activities. In this study, we show global terrestrial carbon exchanges (net ecosystem production, net primary production, and gross primary production) with 1km-grid resolution. As methodology for computing the exchanges, we 1) developed a global 1km-grid climate and satellite dataset based on the approach in Setoyama and Sasai (2013); 2) used the satellite-driven biosphere model (Biosphere model integrating Eco-physiological And Mechanistic approaches using Satellite data: BEAMS) (Sasai et al., 2005, 2007, 2011); 3) simulated the carbon exchanges by using the new dataset and BEAMS by the use of a supercomputer that includes 1280 CPU and 320 GPGPU cores (GOSAT RCF of NIES). As a result, we could develop a global uniform system for realistically estimating terrestrial carbon exchange, and evaluate net ecosystem production in each community level; leading to obtain highly detailed understanding of terrestrial carbon exchanges.

Spatiotemporal distribution and national measurement of the global carbonate carbon sink.

Science.gov (United States)

Li, Huiwen; Wang, Shijie; Bai, Xiaoyong; Luo, Weijun; Tang, Hong; Cao, Yue; Wu, Luhua; Chen, Fei; Li, Qin; Zeng, Cheng; Wang, Mingming

2018-06-21

The magnitudes, spatial distributions and contributions to global carbon budget of the global carbonate carbon sink (CCS) still remain uncertain, allowing the problem of national measurement of CCS remain unresolved which will directly influence the fairness of global carbon markets and emission trading. Here, based on high spatiotemporal resolution ecological, meteorological raster data and chemical field monitoring data, combining highly reliable machine learning algorithm with the thermodynamic dissolution equilibrium model, we estimated the new CCS of 0.89 ± 0.23 petagrams of carbon per year (Pg C yr -1 ), amounting to 74.50% of global net forest sink and accounting for 28.75% of terrestrial sinks or 46.81% of the missing sink. Our measurement for 142 nations of CCS showed that Russia, Canada, China and the USA contribute over half of the global CCS. We also presented the first global fluxes maps of the CCS with spatial resolution of 0.05°, exhibiting two peaks in equatorial regions (10°S to 10°N) and low latitudes (10°N to 35°N) in Northern Hemisphere. By contrast, there are no peaks in Southern Hemisphere. The greatest average carbon sink flux (CCSF), i.e., 2.12 tC ha -1  yr -1 , for 2000 to 2014 was contributed by tropical rainforest climate near the equator, and the smallest average CCSF was presented in tropical arid zones, showing a magnitude of 0.26 tC ha -1  yr -1 . This research estimated the magnitudes, spatial distributions, variations and contributions to the global carbon budget of the CCS in a higher spatiotemporal representativeness and expandability way, which, via multiple mechanisms, introduced an important sink in the terrestrial carbon sink system and the global missing sink and that can help us further reveal and support our understanding of global rock weathering carbon sequestration, terrestrial carbon sink system and global carbon cycle dynamics which make our understanding of global change more comprehensive

The role of forest disturbance in global forest mortality and terrestrial carbon fluxes

Science.gov (United States)

Pugh, Thomas; Arneth, Almut; Smith, Benjamin; Poulter, Benjamin

2017-04-01

Large-scale forest disturbance dynamics such as insect outbreaks, wind-throw and fires, along with anthropogenic disturbances such as logging, have been shown to turn forests from carbon sinks into intermittent sources, often quite dramatically so. There is also increasing evidence that disturbance regimes in many regions are changing as a result of climatic change and human land-management practices. But how these landscape-scale events fit into the wider picture of global tree mortality is not well understood. Do such events dominate global carbon turnover, or are their effects highly regional? How sensitive is global terrestrial carbon exchange to realistic changes in the occurrence rate of such disturbances? Here, we combine recent advances in global satellite observations of stand-replacing forest disturbances and in compilations of forest inventory data, with a global terrestrial ecosystem model which incorporates an explicit representation of the role of disturbance in forest dynamics. We find that stand-replacing disturbances account for a fraction of wood carbon turnover that varies spatially from less than 5% in the tropical rainforest to ca. 50% in the mid latitudes, and as much as 90% in some heavily-managed regions. We contrast the size of the land-atmosphere carbon flux due to this disturbance with other components of the terrestrial carbon budget. In terms of sensitivity, we find a quasi log-linear relationship of disturbance rate to total carbon storage. Relatively small changes in disturbance rates at all latitudes have marked effects on vegetation carbon storage, with potentially very substantial implications for the global terrestrial carbon sink. Our results suggest a surprisingly small effect of disturbance type on large-scale forest vegetation dynamics and carbon storage, with limited evidence of widespread increases in nitrogen limitation as a result of increasing future disturbance. However, the influence of disturbance type on soil carbon

Regionwide Geodynamic Analyses of the Cenozoic Carbonate Burial in Sri Lanka Related to Climate and Atmospheric CO2

Directory of Open Access Journals (Sweden)

Amila Sandaruwan Ratnayake

2016-12-01

Full Text Available Asian tectonism and exhumation are critical components to develop modern icehouse climate. In this study, stratigraphic sections of eight wells in the Mannar and Cauvery basins were considered. The author demonstrated that this local system records a wealth of information to understated regional and global paleoclimatic trends over the Cenozoic era. The lithostratigraphic framework has been generally characterized by deposition of carbonate-rich sediments since the Middle Cenozoic. Geological provenance of carbonate sediments had probably related to local sources from Sri Lankan and Indian land masses. The main controlling factor of carbonate burial is rather questionable. However, this carbonate burial has indicated the possible link to the Middle to Late Cenozoic global climatic transition. This major climatic shift was characterized by long-term reduction of atmospheric carbon dioxide concentration over the Cenozoic era. Consequently, this geological trend (carbonate burial has a straightforward teleconnection to the global cooling towards the glaciated earth followed by the development of polar ice sheets that persist today.

Daily and Hourly Variability in Global Fire Emissions and Consequences for Atmospheric Model Predictions of Carbon Monoxide

Science.gov (United States)

Mu, M.; Randerson, J. T.; van der Werf, G. R.; Giglio, L.; Kasibhatla, P.; Morton, D.; Collatz, G. J.; DeFries, R. S.; Hyer, E. J.; Prins, E. M.;

Carbon Dioxide Information Analysis Center and World Data Center for Atmospheric Trace Gases, Fiscal Year 2002 Annual Report

Energy Technology Data Exchange (ETDEWEB)

Cushman, R.M.

2003-08-28

The Carbon Dioxide Information Analysis Center (CDIAC), which includes the World Data Center (WDC) for Atmospheric Trace Gases, is the primary global change data and information analysis center of the U.S. Department of Energy (DOE). More than just an archive of data sets and publications, CDIAC has, since its inception in 1982, enhanced the value of its holdings through intensive quality assurance, documentation, and integration. Whereas many traditional data centers are discipline-based (for example, meteorology or oceanography), CDIAC's scope includes potentially anything and everything that would be of value to users concerned with the greenhouse effect and global climate change, including atmospheric concentrations and atmospheric emissions of carbon dioxide (CO{sub 2}) and other radiatively active gases; the role of the terrestrial biosphere and the oceans in the biogeochemical cycles of greenhouse gases; long-term climate trends; the effects of elevated CO{sub 2} on vegetation; and the vulnerability of coastal areas to rising sea levels.

Stable isotopic constraints on global soil organic carbon turnover

Science.gov (United States)

Wang, Chao; Houlton, Benjamin Z.; Liu, Dongwei; Hou, Jianfeng; Cheng, Weixin; Bai, Edith

2018-02-01

Carbon dioxide release during soil organic carbon (SOC) turnover is a pivotal component of atmospheric CO2 concentrations and global climate change. However, reliably measuring SOC turnover rates on large spatial and temporal scales remains challenging. Here we use a natural carbon isotope approach, defined as beta (β), which was quantified from the δ13C of vegetation and soil reported in the literature (176 separate soil profiles), to examine large-scale controls of climate, soil physical properties and nutrients over patterns of SOC turnover across terrestrial biomes worldwide. We report a significant relationship between β and calculated soil C turnover rates (k), which were estimated by dividing soil heterotrophic respiration rates by SOC pools. ln( - β) exhibits a significant linear relationship with mean annual temperature, but a more complex polynomial relationship with mean annual precipitation, implying strong-feedbacks of SOC turnover to climate changes. Soil nitrogen (N) and clay content correlate strongly and positively with ln( - β), revealing the additional influence of nutrients and physical soil properties on SOC decomposition rates. Furthermore, a strong (R2 = 0.76; p turnover and thereby improving predictions of multiple global change influences over terrestrial C-climate feedback.

Contributions to accelerating atmospheric CO2 growth from economic activity, carbon intensity, and efficiency of natural sinks

International Nuclear Information System (INIS)

Canadella, J.G.; Raupacha, M.R.; Le Quere, C.; Buitenhuis, E.T.; Gillett, N.P.; Field, C.B.; Ciais, P.; Conway, T.J.; Houghton, R.A.; Marland, G.

2007-01-01

The growth rate of atmospheric carbon dioxide (CO2), the largest human contributor to human-induced climate change, is increasing rapidly. Three processes contribute to this rapid increase. Two of these processes concern emissions. Recent growth of the world economy combined with an increase in its carbon intensity have led to rapid growth in fossil fuel CO2 emissions since 2000: comparing the 1990s with 2000-2006, the emissions growth rate increased from 1.3% to 3.3%/y. The third process is indicated by increasing evidence (P 0.89) for a long-term (50-year) increase in the airborne fraction (AF) of CO2 emissions, implying a decline in the efficiency of CO2 sinks on land and oceans in absorbing anthropogenic emissions. Since 2000, the contributions of these three factors to the increase in the atmospheric CO2 growth rate have been ∼65 ± 16% from increasing global economic activity, 17 ± 6% from the increasing carbon intensity of the global economy, and 18 ± 15% from the increase in AF. An increasing AF is consistent with results of climate-carbon cycle models, but the magnitude of the observed signal appears larger than that estimated by models. All of these changes characterize a carbon cycle that is generating stronger-than-expected and sooner-than-expected climate forcing. airborne fraction anthropogenic carbon emissions carbon-climate feedback terrestrial and ocean carbon emissions vulnerabilities of the carbon cycle

Global warming and carbon taxation. Optimal policy and the role of administration costs

International Nuclear Information System (INIS)

Williams, M.

1995-01-01

This paper develops a model relating CO 2 emissions to atmosphere concentrations, global temperature change and economic damages. For a variety of parameter assumptions, the model provides estimates of the marginal cost of emissions in various years. The optimal carbon tax is a function of the marginal emission cost and the costs of administering the tax. This paper demonstrates that under any reasonable assumptions, the optimal carbon tax is zero for at least several decades. (author)

Simulating forest productivity and surface-atmosphere carbon exchange in the BOREAS study region

Energy Technology Data Exchange (ETDEWEB)

Kimball, J.S.; Thornton, P.E.; White, M.A.; Running, S.W. [Montana Univ., Missoula, MT (United States). School of Forestry

1997-12-31

Studies have shown that the boreal forest region is in danger of experiencing significant warming and drying in response to increases in atmospheric CO{sub 2} concentration and other greenhouse gases. Since the boreal forest region contains 16-24 per cent of the world`s soil carbon, warming in this region could result in a rapid, large-scale displacement and redistribution of boreal forest, enhanced release of CO{sub 2} to the atmosphere, and an intensification of global warming. A study was conducted in which a process-based, general ecosystem model (BIOME-BGC) was used to simulate daily gross primary production, maintenance and heterotrophic respiration, net primary production and net ecosystem carbon exchange of boreal aspen, jack pine and black spruce. The objective was to integrate point measurements across multiple spatial and temporal scales using process level models of the boreal forest water, energy and biogeochemical cycles. Climate characteristics that control simulated carbon fluxes were also studied. Results showed that trees with large daily evapotranspiration rates and those situated on sandy soils with low water holding capacities were especially vulnerable to increased temperature and drought conditions. Trees subject to frequent water stress during the growing season, particularly older trees that exhibit low photosynthetic and high respiration rates, were on the margin between being annual net sources or sinks for atmospheric carbon. 71 refs., 3 tabs., 5 figs.

The carbon footprint of global tourism

Science.gov (United States)

Lenzen, Manfred; Sun, Ya-Yen; Faturay, Futu; Ting, Yuan-Peng; Geschke, Arne; Malik, Arunima

2018-06-01

Tourism contributes significantly to global gross domestic product, and is forecast to grow at an annual 4%, thus outpacing many other economic sectors. However, global carbon emissions related to tourism are currently not well quantified. Here, we quantify tourism-related global carbon flows between 160 countries, and their carbon footprints under origin and destination accounting perspectives. We find that, between 2009 and 2013, tourism's global carbon footprint has increased from 3.9 to 4.5 GtCO2e, four times more than previously estimated, accounting for about 8% of global greenhouse gas emissions. Transport, shopping and food are significant contributors. The majority of this footprint is exerted by and in high-income countries. The rapid increase in tourism demand is effectively outstripping the decarbonization of tourism-related technology. We project that, due to its high carbon intensity and continuing growth, tourism will constitute a growing part of the world's greenhouse gas emissions.

Sources of uncertainties in modelling black carbon at the global scale

Directory of Open Access Journals (Sweden)

E. Vignati

2010-03-01

Full Text Available Our understanding of the global black carbon (BC cycle is essentially qualitative due to uncertainties in our knowledge of its properties. This work investigates two source of uncertainties in modelling black carbon: those due to the use of different schemes for BC ageing and its removal rate in the global Transport-Chemistry model TM5 and those due to the uncertainties in the definition and quantification of the observations, which propagate through to both the emission inventories, and the measurements used for the model evaluation.

The schemes for the atmospheric processing of black carbon that have been tested with the model are (i a simple approach considering BC as bulk aerosol and a simple treatment of the removal with fixed 70% of in-cloud black carbon concentrations scavenged by clouds and removed when rain is present and (ii a more complete description of microphysical ageing within an aerosol dynamics model, where removal is coupled to the microphysical properties of the aerosol, which results in a global average of 40% in-cloud black carbon that is scavenged in clouds and subsequently removed by rain, thus resulting in a longer atmospheric lifetime. This difference is reflected in comparisons between both sets of modelled results and the measurements. Close to the sources, both anthropogenic and vegetation fire source regions, the model results do not differ significantly, indicating that the emissions are the prevailing mechanism determining the concentrations and the choice of the aerosol scheme does not influence the levels. In more remote areas such as oceanic and polar regions the differences can be orders of magnitude, due to the differences between the two schemes. The more complete description reproduces the seasonal trend of the black carbon observations in those areas, although not always the magnitude of the signal, while the more simplified approach underestimates black carbon concentrations by orders of

Exponential growth and atmospheric carbon dioxide

International Nuclear Information System (INIS)

Laurmann, J.A.; Rotty, R.M.

1983-01-01

The adequacy of assumptions required to project atmospheric CO 2 concentrations in time frames of practical importance is reviewed. Relevant issues concern the form assumed for future fossil fuel release, carbon cycle approximations, and the implications of revisions in fossil fuel patterns required to maintain atmospheric CO 2 levels below a chosen threshold. In general, we find that with a judiciously selected exponential fossil fuel release rate, and with a constant airborn fraction, we can estimate atmospheric CO 2 growth over the next 50 years based on essentially surprise free scenarios. Resource depletion effects must be included for projections beyond about 50 years, and on this time frame the constant airborne fraction approximation has to be questioned as well (especially in later years when the fossil fuel use begins to taper off). For projections for over 100 years, both energy demand scenarios and currently available carbon cycle models have sufficient uncertainties that atmospheric CO 2 levels derived from them are not much better than guesses

Carbon isotopic evidence for the associations of decreasing atmospheric CO2 level with the Frasnian-Famennian mass extinction

Science.gov (United States)

Xu, Bing; Gu, Zhaoyan; Wang, Chengyuan; Hao, Qingzhen; Han, Jingtai; Liu, Qiang; Wang, Luo; Lu, Yanwu

2012-03-01

A perturbation of the global carbon cycle has often been used for interpreting the Frasnian-Famennian (F-F) mass extinction. However, the changes of atmospheric CO2 level (pCO2) during this interval are much debatable. To illustrate the carbon cycle during F-F transition, paired inorganic (δ13Ccarb) and organic (δ13Corg) carbon isotope analyses were carried out on two late Devonian carbonate sequences (Dongcun and Yangdi) from south China. The larger amplitude shift of δ13Corg compared to δ13Ccarb and its resultant Δ13C (Δ13C = δ13Ccarb - δ13Corg) decrease indicate decreased atmospheric CO2level around the F-F boundary. The onset ofpCO2 level decrease predates that of marine regressions, which coincide with the beginning of conodont extinctions, suggesting that temperature decrease induced by decreased greenhouse effect of atmospheric CO2might have contributed to the F-F mass extinction.

Subterranean karst environments as a global sink for atmospheric methane

Science.gov (United States)

Webster, Kevin D.; Drobniak, Agnieszka; Etiope, Giuseppe; Mastalerz, Maria; Sauer, Peter E.; Schimmelmann, Arndt

2018-03-01

The air in subterranean karst cavities is often depleted in methane (CH4) relative to the atmosphere. Karst is considered a potential sink for the atmospheric greenhouse gas CH4 because its subsurface drainage networks and solution-enlarged fractures facilitate atmospheric exchange. Karst landscapes cover about 14% of earth's continental surface, but observations of CH4 concentrations in cave air are limited to localized studies in Gibraltar, Spain, Indiana (USA), Vietnam, Australia, and by incomplete isotopic data. To test if karst is acting as a global CH4 sink, we measured the CH4 concentrations, δ13CCH4, and δ2HCH4 values of cave air from 33 caves in the USA and three caves in New Zealand. We also measured CO2 concentrations, δ13CCO2, and radon (Rn) concentrations to support CH4 data interpretation by assessing cave air residence times and mixing processes. Among these caves, 35 exhibited subatmospheric CH4 concentrations in at least one location compared to their local atmospheric backgrounds. CH4 concentrations, δ13CCH4, and δ2HCH4 values suggest that microbial methanotrophy within caves is the primary CH4 consumption mechanism. Only 5 locations from 3 caves showed elevated CH4 concentrations compared to the atmospheric background and could be ascribed to local CH4 sources from sewage and outgassing swamp water. Several associated δ13CCH4 and δ2HCH4 values point to carbonate reduction and acetate fermentation as biochemical pathways of limited methanogenesis in karst environments and suggest that these pathways occur in the environment over large spatial scales. Our data show that karst environments function as a global CH4 sink.

Carbon Flux to the Atmosphere from Land-Use Changes: 1850 to 1990

Energy Technology Data Exchange (ETDEWEB)

Houghton, R.A.

2001-02-22

The database documented in this numeric data package, a revision to a database originally published by the Carbon Dioxide Information Analysis Center (CDIAC) in 1995, consists of annual estimates, from 1850 through 1990, of the net flux of carbon between terrestrial ecosystems and the atmosphere resulting from deliberate changes in land cover and land use, especially forest clearing for agriculture and the harvest of wood for wood products or energy. The data are provided on a year-by-year basis for nine regions (North America, South and Central America, Europe, North Africa and the Middle East, Tropical Africa, the Former Soviet Union, China, South and Southeast Asia, and the Pacific Developed Region) and the globe. Some data begin earlier than 1850 (e.g., for six regions, areas of different ecosystems are provided for the year 1700) or extend beyond 1990 (e.g., fuelwood harvest in South and Southeast Asia, by forest type, is provided through 1995). The global net flux during the period 1850 to 1990 was 124 Pg of carbon (1 petagram = 10{sup 15} grams). During this period, the greatest regional flux was from South and Southeast Asia (39 Pg of carbon), while the smallest regional flux was from North Africa and the Middle East (3 Pg of carbon). For the year 1990, the global total net flux was estimated to be 2.1 Pg of carbon.

Changes of global terrestrial carbon budget and major drivers in recent 30 years simulated using the remote sensing driven BEPS model

Science.gov (United States)

Ju, W.; Chen, J.; Liu, R.; Liu, Y.

2013-12-01

The process-based Boreal Ecosystem Productivity Simulator (BEPS) model was employed in conjunction with spatially distributed leaf area index (LAI), land cover, soil, and climate data to simulate the carbon budget of global terrestrial ecosystems during the period from 1981 to 2008. The BEPS model was first calibrated and validated using gross primary productivity (GPP), net primary productivity (NPP), and net ecosystem productivity (NEP) measured in different ecosystems across the word. Then, four global simulations were conducted at daily time steps and a spatial resolution of 8 km to quantify the global terrestrial carbon budget and to identify the relative contributions of changes in climate, atmospheric CO2 concentration, and LAI to the global terrestrial carbon sink. The long term LAI data used to drive the model was generated through fusing Moderate Resolution Imaging Spectroradiometer (MODIS) and historical Advanced Very High Resolution Radiometer (AVHRR) data pixel by pixel. The meteorological fields were interpolated from the 0.5° global daily meteorological dataset produced by the land surface hydrological research group at Princeton University. The results show that the BEPS model was able to simulate carbon fluxes in different ecosystems. Simulated GPP, NPP, and NEP values and their temporal trends exhibited distinguishable spatial patterns. During the period from 1981 to 2008, global terrestrial ecosystems acted as a carbon sink. The averaged global totals of GPP NPP, and NEP were 122.70 Pg C yr-1, 56.89 Pg C yr-1, and 2.76 Pg C yr-1, respectively. The global totals of GPP and NPP increased greatly, at rates of 0.43 Pg C yr-2 (R2=0.728) and 0.26 Pg C yr-2 (R2=0.709), respectively. Global total NEP did not show an apparent increasing trend (R2= 0.036), averaged 2.26 Pg C yr-1, 3.21 Pg C yr-1, and 2.72 Pg C yr-1 for the periods from 1981 to 1989, from 1990 to 1999, and from 2000 to 2008, respectively. The magnitude and temporal trend of global

Carbon isotope ratios of atmospheric carbon dioxide

International Nuclear Information System (INIS)

Sakai, Hitoshi; Kishima, Noriaki; Tsutaki, Yasuhiro.

1982-01-01

The delta 13 C values relative to PDB were measured for carbon dioxide in air samples collected at various parts of Japan and at Mauna Loa Observatory, Hawaii in the periods of 1977 and 1978. The delta 13 C values of the ''clean air'' are -7.6 % at Hawaii and -8.1 per mille Oki and Hachijo-jima islands. These values are definitely lighter than the carbon isotope ratios (-6.9 per mille) obtained by Keeling for clean airs collected at Southern California in 1955 to 1956. The increase in 12 C in atmospheric carbon dioxide is attributed to the input of the anthropogenic light carbon dioxides (combustion of fossil fuels etc.) Taking -7.6 per mille to be the isotope ratio of CO 2 in the present clean air, a simple three box model predicts that the biosphere has decreased rather than increased since 1955, implying that it is acting as the doner of carbon rather than the sink. (author)

Atlas of the global distribution of atmospheric heating during the global weather experiment

Science.gov (United States)

Schaack, Todd K.; Johnson, Donald R.

1991-01-01

Global distributions of atmospheric heating for the annual cycle of the Global Weather Experiment are estimated from the European Centre for Medium-Range Weather Forecasts (ECMWF) Level 3b data set. Distributions of monthly, seasonally, and annually averaged heating are presented for isentropic and isobaric layers within the troposphere and for the troposphere as a whole. The distributions depict a large-scale structure of atmospheric heating that appears spatially and temporally consistent with known features of the global circulation and the seasonal evolution.

Carbon sequestration in wood and paper products

Science.gov (United States)

Kenneth E. Skog; Geraldine A. Nicholson

2000-01-01

Recognition that increasing levels of CO2 in the atmosphere will affect the global climate has spurred research into reduction global carbon emissions and increasing carbon sequestration. The main nonhuman sources of atmospheric CO2 are animal respiration and decay of biomass. However, increases in atmospheric levels are...

Carbon Dioxide Information Analysis Center and World Data Center for Atmospheric Trace Gases Fiscal Year 2000 Annual Report

Energy Technology Data Exchange (ETDEWEB)

Cushman, R.M.

2001-11-15

The Carbon Dioxide Information Analysis Center (CDIAC), which includes the World Data Center (WDC) for Atmospheric Trace Gases, is the primary global change data and information analysis center of the U.S. Department of Energy (DOE). More than just an archive of data sets and publications, CDIAC has, since its inception in 1982, enhanced the value of its holdings through intensive quality assurance, documentation, and integration. Whereas many traditional data centers are discipline-based (for example, meteorology or oceanography), CDIAC's scope includes potentially anything and everything that would be of value to users concerned with the greenhouse effect and global climate change, including concentrations of carbon dioxide (CO{sub 2}) and other radiatively active gases in the atmosphere; the role of the terrestrial biosphere and the oceans in the biogeochemical cycles of greenhouse gases; emissions of CO{sub 2} and other trace gases to the atmosphere; long-term climate trends; the effects of elevated CO{sub 2} on vegetation; and the vulnerability of coastal areas to rising sea levels.

Higher Atmosphere Heating due to black carbon Over the Northern Part of India

Science.gov (United States)

Tiwari, S.; Singh, S., , Dr

2017-12-01

Light-absorbing, atmospheric particles have gained greater attention in recent years because of their direct and indirect impacts on regional and global climate. Atmospheric black carbon (BC) aerosol (also called soot particle) is a leading climate warming agent, yet uncertainties in the global direct aerosol radiative forcing remain large. Based on a year of aerosol absorption measurements at seven wavelengths, BC concentrations were investigated in Dhanbad, the coal capital of India. Coal is routinely burned for cooking and residential heat as well as in small industries. The mean daily concentrations of ultraviolet-absorbing black carbon measured at 370 nm (UVBC) and black carbon measured at 880 nm (BC) were 9.8 ± 5.7 and 6.5 ± 3.8 μg m-3, respectively. The difference between UVBC and BC, Delta-C, is an indicator of biomass or residential coal burning and averaged 3.29 ± 4.61 μg m-3. An alternative approach uses the calculation of the Angstrom Exponent (AE) to estimate the amounts of biomass/coal and traffic BC. Biomass/coal burning contributed 87% and fossil fuel combustion contributed 13% to the annual average BC concentration. In the post-monsoon season, potential source contribution function analysis showed that air masses came from the central and northwestern Indo-Gangetic Plains resulting in mean UVBC values of 10.9 μg m-3 and BC of 7.2 μg m-3. The mean winter UVBC and BC concentrations were 15.0 and 10.1 μg m-3, respectively. These highest values were largely driven by local sources under conditions of poor dispersion. The direct radiative forcing (DRF) due to UVBC and BC at the surface (SFC) and the top of the atmosphere (TOA) were calculated. The mean atmospheric heating rates due to UVBC and BC were estimated to be 1.40°K day-1 and 1.18°K day-1, respectively. This high heating rate may affect the monsoon circulation in this region.

Global change and modern coral reefs: New opportunities to understand shallow-water carbonate depositional processes

Science.gov (United States)

Hallock, Pamela

2005-04-01

Human activities are impacting coral reefs physically, biologically, and chemically. Nutrification, sedimentation, chemical pollution, and overfishing are significant local threats that are occurring worldwide. Ozone depletion and global warming are triggering mass coral-bleaching events; corals under temperature stress lose the ability to synthesize protective sunscreens and become more sensitive to sunlight. Photo-oxidative stress also reduces fitness, rendering reef-building organisms more susceptible to emerging diseases. Increasing concentration of atmospheric CO 2 has already reduced CaCO 3 saturation in surface waters by more than 10%. Doubling of atmospheric CO 2 concentration over pre-industrial concentration in the 21st century may reduce carbonate production in tropical shallow marine environments by as much as 80%. As shallow-water reefs decline worldwide, opportunities abound for researchers to expand understanding of carbonate depositional systems. Coordinated studies of carbonate geochemistry with photozoan physiology and calcification, particularly in cool subtropical-transition zones between photozoan-reef and heterotrophic carbonate-ramp communities, will contribute to understanding of carbonate sedimentation under environmental change, both in the future and in the geologic record. Cyanobacteria are becoming increasingly prominent on declining reefs, as these microbes can tolerate strong solar radiation, higher temperatures, and abundant nutrients. The responses of reef-dwelling cyanobacteria to environmental parameters associated with global change are prime topics for further research, with both ecological and geological implications.

Comment on "Scrutinizing the carbon cycle and CO2residence time in the atmosphere" by H. Harde

Science.gov (United States)

Köhler, Peter; Hauck, Judith; Völker, Christoph; Wolf-Gladrow, Dieter A.; Butzin, Martin; Halpern, Joshua B.; Rice, Ken; Zeebe, Richard E.

2018-05-01

Harde (2017) proposes an alternative accounting scheme for the modern carbon cycle and concludes that only 4.3% of today's atmospheric CO2 is a result of anthropogenic emissions. As we will show, this alternative scheme is too simple, is based on invalid assumptions, and does not address many of the key processes involved in the global carbon cycle that are important on the timescale of interest. Harde (2017) therefore reaches an incorrect conclusion about the role of anthropogenic CO2 emissions. Harde (2017) tries to explain changes in atmospheric CO2 concentration with a single equation, while the most simple model of the carbon cycle must at minimum contain equations of at least two reservoirs (the atmosphere and the surface ocean), which are solved simultaneously. A single equation is fundamentally at odds with basic theory and observations. In the following we will (i) clarify the difference between CO2 atmospheric residence time and adjustment time, (ii) present recently published information about anthropogenic carbon, (iii) present details about the processes that are missing in Harde (2017), (iv) briefly discuss shortcoming in Harde's generalization to paleo timescales, (v) and comment on deficiencies in some of the literature cited in Harde (2017).

Atmospheric analyzer, carbon monoxide monitor and toluene diisocyanate monitor

Science.gov (United States)

Shannon, A. V.

1977-01-01

The purpose of the atmospheric analyzer and the carbon monoxide and toluene diisocyanate monitors is to analyze the atmospheric volatiles and to monitor carbon monoxide and toluene diisocyanate levels in the cabin atmosphere of Skylab. The carbon monoxide monitor was used on Skylab 2, 3, and 4 to detect any carbon monoxide levels above 25 ppm. Air samples were taken once each week. The toluene diisocyanate monitor was used only on Skylab 2. The loss of a micrometeoroid shield following the launch of Skylab 1 resulted in overheating of the interior walls of the Orbital Workshop. A potential hazard existed from outgassing of an isocyanate derivative resulting from heat-decomposition of the rigid polyurethane wall insulation. The toluene diisocyanate monitor was used to detect any polymer decomposition. The atmospheric analyzer was used on Skylab 4 because of a suspected leak in the Skylab cabin. An air sample was taken at the beginning, middle, and the end of the mission.

Tropical rainforests dominate multi-decadal variability of the global carbon cycle

Science.gov (United States)

Zhang, X.; Wang, Y. P.; Peng, S.; Rayner, P. J.; Silver, J.; Ciais, P.; Piao, S.; Zhu, Z.; Lu, X.; Zheng, X.

2017-12-01

Recent studies find that inter-annual variability of global atmosphere-to-land CO2 uptake (NBP) is dominated by semi-arid ecosystems. However, the NBP variations at decadal to multi-decadal timescales are still not known. By developing a basic theory for the role of net primary production (NPP) and heterotrophic respiration (Rh) on NBP and applying it to 100-year simulations of terrestrial ecosystem models forced by observational climate, we find that tropical rainforests dominate the multi-decadal variability of global NBP (48%) rather than the semi-arid lands (35%). The NBP variation at inter-annual timescales is almost 90% contributed by NPP, but across longer timescales is progressively controlled by Rh that constitutes the response from the NPP-derived soil carbon input (40%) and the response of soil carbon turnover rates to climate variability (60%). The NBP variations of tropical rainforests is modulated by the ENSO and the PDO through their significant influences on temperature and precipitation at timescales of 2.5-7 and 25-50 years, respectively. This study highlights the importance of tropical rainforests on the multi-decadal variability of global carbon cycle, suggesting that we need to carefully differentiate the effect of NBP long-term fluctuations associated with ocean-related climate modes on the long-term trend in land sink.

Estimating global "blue carbon" emissions from conversion and degradation of vegetated coastal ecosystems.

Directory of Open Access Journals (Sweden)

Linwood Pendleton

Full Text Available Recent attention has focused on the high rates of annual carbon sequestration in vegetated coastal ecosystems--marshes, mangroves, and seagrasses--that may be lost with habitat destruction ('conversion'. Relatively unappreciated, however, is that conversion of these coastal ecosystems also impacts very large pools of previously-sequestered carbon. Residing mostly in sediments, this 'blue carbon' can be released to the atmosphere when these ecosystems are converted or degraded. Here we provide the first global estimates of this impact and evaluate its economic implications. Combining the best available data on global area, land-use conversion rates, and near-surface carbon stocks in each of the three ecosystems, using an uncertainty-propagation approach, we estimate that 0.15-1.02 Pg (billion tons of carbon dioxide are being released annually, several times higher than previous estimates that account only for lost sequestration. These emissions are equivalent to 3-19% of those from deforestation globally, and result in economic damages of $US 6-42 billion annually. The largest sources of uncertainty in these estimates stems from limited certitude in global area and rates of land-use conversion, but research is also needed on the fates of ecosystem carbon upon conversion. Currently, carbon emissions from the conversion of vegetated coastal ecosystems are not included in emissions accounting or carbon market protocols, but this analysis suggests they may be disproportionally important to both. Although the relevant science supporting these initial estimates will need to be refined in coming years, it is clear that policies encouraging the sustainable management of coastal ecosystems could significantly reduce carbon emissions from the land-use sector, in addition to sustaining the well-recognized ecosystem services of coastal habitats.

Impacts of 2°C global warming on primary production and soil carbon storage capacity at pan-European level

Directory of Open Access Journals (Sweden)

Abdulla Sakalli

2017-08-01

Full Text Available Atmospheric CO2 has been dramatically increasing since beginning of the industrial time (i.e. 1860, being one of the main driver for climate change at regional and global level. The change in CO2 concentration in the atmosphere, together with that of temperature, precipitation and/or so radiation, can influence the biogeochemical cycles in all ecosystems. In this study, we investigate the combined effect of CO2 concentration and six climate variables on carbon uptake, i.e., gross primary production (GPP and carbon storage, i.e, soil carbon (SoilC in terrestrial biosphere by using the Community Land Model (CLM vers. 4.5 and evaluate the model’s results against available observation data. We also analysed the change in carbon uptake and storage under a 2°C global mean warming. Results show that the model performed reasonably well for GPP and SoilC at pan-European scale. We also found a positive correlation between GPP, precipitation and surface wind, and a negative correlation between GPP and surface downwelling longwave radiation (rlds. Under a 2°C global warming, GPP and SoilC show an increase, an average, of about 20%, and 5% at pan-European scale, respectively. However, our results indicate that CLM4.5 may need improvements particularly in carbon-nitrogen interaction and carbon accumulation in soil.

NOAA/NCEP Global Forecast System (GFS) Atmospheric Model

Data.gov (United States)

National Oceanic and Atmospheric Administration, Department of Commerce — U.S. National Oceanic and Atmospheric Administration (NOAA) National Centers for Environmental Prediction (NCEP) Global Forecast System (GFS) numerical weather...

Global Tree Cover and Biomass Carbon on Agricultural Land: The contribution of agroforestry to global and national carbon budgets.

Science.gov (United States)

Zomer, Robert J; Neufeldt, Henry; Xu, Jianchu; Ahrends, Antje; Bossio, Deborah; Trabucco, Antonio; van Noordwijk, Meine; Wang, Mingcheng

2016-07-20

Agroforestry systems and tree cover on agricultural land make an important contribution to climate change mitigation, but are not systematically accounted for in either global carbon budgets or national carbon accounting. This paper assesses the role of trees on agricultural land and their significance for carbon sequestration at a global level, along with recent change trends. Remote sensing data show that in 2010, 43% of all agricultural land globally had at least 10% tree cover and that this has increased by 2% over the previous ten years. Combining geographically and bioclimatically stratified Intergovernmental Panel on Climate Change (IPCC) Tier 1 default estimates of carbon storage with this tree cover analysis, we estimated 45.3 PgC on agricultural land globally, with trees contributing >75%. Between 2000 and 2010 tree cover increased by 3.7%, resulting in an increase of >2 PgC (or 4.6%) of biomass carbon. On average, globally, biomass carbon increased from 20.4 to 21.4 tC ha(-1). Regional and country-level variation in stocks and trends were mapped and tabulated globally, and for all countries. Brazil, Indonesia, China and India had the largest increases in biomass carbon stored on agricultural land, while Argentina, Myanmar, and Sierra Leone had the largest decreases.

Geography of Global Forest Carbon Stocks & Dynamics

Science.gov (United States)

Saatchi, S. S.; Yu, Y.; Xu, L.; Yang, Y.; Fore, A.; Ganguly, S.; Nemani, R. R.; Zhang, G.; Lefsky, M. A.; Sun, G.; Woodall, C. W.; Naesset, E.; Seibt, U. H.

2014-12-01

Spatially explicit distribution of carbon stocks and dynamics in global forests can greatly reduce the uncertainty in the terrestrial portion of the global carbon cycle by improving estimates of emissions and uptakes from land use activities, and help with green house gas inventory at regional and national scales. Here, we produce the first global distribution of carbon stocks in living woody biomass at ~ 100 m (1-ha) resolution for circa 2005 from a combination of satellite observations and ground inventory data. The total carbon stored in live woody biomass is estimated to be 337 PgC with 258 PgC in aboveground and 79 PgC in roots, and partitioned globally in boreal (20%), tropical evergreen (50%), temperate (12%), and woodland savanna and shrublands (15%). We use a combination of satellite observations of tree height, remote sensing data on deforestation and degradation to quantify the dynamics of these forests at the biome level globally and provide geographical distribution of carbon storage dynamics in terms sinks and sources globally.

The CarbonTracker Data Assimilation Shell (CTDAS) v1.0: implementation and global carbon balance 2001-2015

Science.gov (United States)

van der Laan-Luijkx, Ingrid T.; van der Velde, Ivar R.; van der Veen, Emma; Tsuruta, Aki; Stanislawska, Karolina; Babenhauserheide, Arne; Zhang, Hui Fang; Liu, Yu; He, Wei; Chen, Huilin; Masarie, Kenneth A.; Krol, Maarten C.; Peters, Wouter

2017-07-01

Data assimilation systems are used increasingly to constrain the budgets of reactive and long-lived gases measured in the atmosphere. Each trace gas has its own lifetime, dominant sources and sinks, and observational network (from flask sampling and in situ measurements to space-based remote sensing) and therefore comes with its own optimal configuration of the data assimilation. The CarbonTracker Europe data assimilation system for CO2 estimates global carbon sources and sinks, and updates are released annually and used in carbon cycle studies. CarbonTracker Europe simulations are performed using the new modular implementation of the data assimilation system: the CarbonTracker Data Assimilation Shell (CTDAS). Here, we present and document this redesign of the data assimilation code that forms the heart of CarbonTracker, specifically meant to enable easy extension and modification of the data assimilation system. This paper also presents the setup of the latest version of CarbonTracker Europe (CTE2016), including the use of the gridded state vector, and shows the resulting carbon flux estimates. We present the distribution of the carbon sinks over the hemispheres and between the land biosphere and the oceans. We show that with equal fossil fuel emissions, 2015 has a higher atmospheric CO2 growth rate compared to 2014, due to reduced net land carbon uptake in later year. The European carbon sink is especially present in the forests, and the average net uptake over 2001-2015 was 0. 17 ± 0. 11 PgC yr-1 with reductions to zero during drought years. Finally, we also demonstrate the versatility of CTDAS by presenting an overview of the wide range of applications for which it has been used so far.

Atomistic modeling of carbon Cottrell atmospheres in bcc iron

Science.gov (United States)

Veiga, R. G. A.; Perez, M.; Becquart, C. S.; Domain, C.

2013-01-01

Atomistic simulations with an EAM interatomic potential were used to evaluate carbon-dislocation binding energies in bcc iron. These binding energies were then used to calculate the occupation probability of interstitial sites in the vicinity of an edge and a screw dislocation. The saturation concentration due to carbon-carbon interactions was also estimated by atomistic simulations in the dislocation core and taken as an upper limit for carbon concentration in a Cottrell atmosphere. We obtained a maximum concentration of 10 ± 1 at.% C at T = 0 K within a radius of 1 nm from the dislocation lines. The spatial carbon distributions around the line defects revealed that the Cottrell atmosphere associated with an edge dislocation is denser than that around a screw dislocation, in contrast with the predictions of the classical model of Cochardt and colleagues. Moreover, the present Cottrell atmosphere model is in reasonable quantitative accord with the three-dimensional atom probe data available in the literature.

Daily and 3-hourly Variability in Global Fire Emissions and Consequences for Atmospheric Model Predictions of Carbon Monoxide

Science.gov (United States)

Mu, M.; Randerson, J. T.; vanderWerf, G. R.; Giglio, L.; Kasibhatla, P.; Morton, D.; Collatz, G. J.; DeFries, R. S.; Hyer, E. J.; Prins, E. M.;

Carbon Dioxide Information Analysis Center and World Data Center for Atmospheric Trace Gases Fiscal Year 2000 Annual Report; ANNUAL

International Nuclear Information System (INIS)

Cushman, R.M.

2001-01-01

The Carbon Dioxide Information Analysis Center (CDIAC), which includes the World Data Center (WDC) for Atmospheric Trace Gases, is the primary global change data and information analysis center of the U.S. Department of Energy (DOE). More than just an archive of data sets and publications, CDIAC has, since its inception in 1982, enhanced the value of its holdings through intensive quality assurance, documentation, and integration. Whereas many traditional data centers are discipline-based (for example, meteorology or oceanography), CDIAC's scope includes potentially anything and everything that would be of value to users concerned with the greenhouse effect and global climate change, including concentrations of carbon dioxide (CO(sub 2)) and other radiatively active gases in the atmosphere; the role of the terrestrial biosphere and the oceans in the biogeochemical cycles of greenhouse gases; emissions of CO(sub 2) and other trace gases to the atmosphere; long-term climate trends; the effects of elevated CO(sub 2) on vegetation; and the vulnerability of coastal areas to rising sea levels

Exploring diurnal and seasonal characteristics of global carbon cycle with GISS Model E2 GCM

Science.gov (United States)

Aleinov, I. D.; Kiang, N. Y.; Romanou, A.

2017-12-01

The ability to properly model surface carbon fluxes on the diurnal and seasonal time scale is a necessary requirement for understanding of the global carbon cycle. It is also one of the most challenging tasks faced by modern General Circulation Models (GCMs) due to complexity of the algorithms and variety of relevant spatial and temporal scales. The observational data, though abundant, is difficult to interpret at the global scale, because flux tower observations are very sparse for large impact areas (such as Amazon and African rainforest and most of Siberia) and satellite missions often struggle to produce sufficiently high confidence data over the land and may be missing CO2 amounts near the surface due to the nature of the method. In this work we use the GISS Model E2 GCM to perform a subset of experiments proposed by the Coupled Climate-Carbon Cycle Model Intercomparison Project (C4MIP) and relate the results to available observations.The GISS Model E2 GCM is currently equipped with a complete global carbon cycle algorithm. Its surface carbon fluxes are computed by the Ent Terrestrial Biosphere Model (Ent TBM) over the land with observed leaf area index of the Moderate Resolution Imaging Spectrometer (MODIS) and by the NASA Ocean Biogeochemistry Model (NOBM) over the ocean. The propagation of atmospheric CO2 is performed by a generic Model E2 tracer algorithm, which is based on a quadratic upstream method (Prather 1986). We perform a series spin-up experiments for preindustrial climate conditions and fixed preindustrial atmospheric CO2 concentration. First, we perform separate spin-up simulations each for terrestrial and ocean carbon. We then combine the spun-up states and perform a coupled spin-up simulation until the model reaches a sufficient equilibrium. We then release restrictions on CO2 concentration and allow it evolve freely, driven only by simulated surface fluxes. We then study the results of the unforced run, comparing the amplitude and the phase

Biomass burning studies and the International Global Atmospheric Chemistry (IGAC) Project

International Nuclear Information System (INIS)

Prinn, R.G.

1991-01-01

The perturbations to local and regional atmospheric chemistry caused by biomass burning also have global significance. The International Global Atmospheric Chemistry (IGAC) Project was created by scientists from over twenty countries in response to the growing interest concern about atmospheric chemical changes and their potential impact on mankind. The goal of the IGAC is to develop a fundamental understanding of the natural and anthropogenic processes that determine the chemical composition of the atmosphere and the interactions between atmospheric composition and biospheric and climatic processes. A specific objective is to accurately predict changes over the next century in the composition and chemistry of the global atmosphere. Current activities, leaders and scientists involved are presented in this chapter

Response of a tundra ecosystem to elevated atmospheric carbon dioxide and CO{sub 2}-induced climate change. Annual technical report

Energy Technology Data Exchange (ETDEWEB)

Oechel, W.C.

1992-04-01

Northern ecosystems contain up to 455 Gt of C in the soil active layer and upper permafrost. The soil carbon in these layers is equivalent to approximately 60% of the carbon currently in the atmosphere as CO{sub 2}. Much of this carbon is stored in the soil as dead organic matter. Its fate is subject to the net effects of global change on the plant and soil systems of northern ecosystems. The arctic alone contains about 60 Gt C, 90% of which is present in the soil active layer and upper permafrost. The arctic is assumed to have been a sink for CO{sub 2} during the historic and recent geologic past. The arctic has the potential to be a very large, long-term source or sink of CO{sub 2} with respect to the atmosphere. In situ experimental manipulations of atmospheric CO{sub 2}, indicated that there is little effect of elevated atmospheric CO{sub 2} on leaf level photosynthesis or whole-ecosystem CO{sub 2} flux over the course of weeks to years, respectively. However, there may be longer- term ecosystem responses to elevated CO{sub 2} that could ultimately affect ecosystem CO{sub 2} balance. In addition to atmospheric CO{sub 2}, climate may affect net ecosystem carbon balance. Recent results indicate that the arctic has become a source of CO{sub 2} to the atmosphere. This change coincides with recent climatic variation in the arctic, and suggests a positive feedback of arctic ecosystems on atmospheric CO{sub 2} and global change. The research proposed in this application has four principal aspects: (A) Long-term response of arctic plants and ecosystems to elevated atmospheric CO{sub 2}; (B) Circumpolar patterns of net ecosystem CO{sub 2} flux; (C) In situ controls by temperature and moisture on net ecosystem CO{sub 2} flux; (D) Scaling of CO{sub 2} flux from plot, to landscape, to regional scales (In conjunction with research proposed for NSF support).

Carbon dioxide sequestration by mineral carbonation

NARCIS (Netherlands)

Huijgen, W.J.J.

2007-01-01

The increasing atmospheric carbon dioxide (CO2) concentration, mainly caused by fossil fuel combustion, has lead to concerns about global warming. A possible technology that can contribute to the reduction of carbon dioxide emissions is CO2 sequestration by mineral carbonation. The basic concept

Global Warming: Physics and Facts

International Nuclear Information System (INIS)

Levi, B.G.; Hafemeister, D.; Scribner, R.

1992-01-01

This report contains papers on: A tutorial on global atmospheric energetics and the greenhouse effect; global climate models: what and how; comparison of general circulation models; climate and the earth's radiation budget; temperature and sea level change; short-term climate variability and predictions; the great ocean conveyor; trace gases in the atmosphere: temporal and spatial trends; the geochemical carbon cycle and the uptake of fossil fuel CO 2 ; forestry and global warming; the physical and policy linkages; policy implications of greenhouse warming; options for lowering US carbon dioxide emissions; options for reducing carbon dioxide emissions; and science and diplomacy: a new partnership to protect the environment

The global carbon cycle

International Nuclear Information System (INIS)

Maier-Reimer, E.

1991-01-01

Basic concepts of the global carbon cycle on earth are described; by careful analyses of isotopic ratios, emission history and oceanic ventilation rates are derived, which provide crucial tests for constraining and calibrating models. Effects of deforestation, fertilizing, fossil fuel burning, soil erosion, etc. are quantified and compared, and the oceanic carbon process is evaluated. Oceanic and terrestrial biosphere modifications are discussed and a carbon cycle model is proposed

Bioavailable atmospheric phosphorous supply to the global ocean: a 3-D global modeling study

Science.gov (United States)

Myriokefalitakis, Stelios; Nenes, Athanasios; Baker, Alex R.; Mihalopoulos, Nikolaos; Kanakidou, Maria

2016-12-01

The atmospheric cycle of phosphorus (P) is parameterized here in a state-of-the-art global 3-D chemistry transport model, taking into account primary emissions of total P (TP) and soluble P (DP) associated with mineral dust, combustion particles from natural and anthropogenic sources, bioaerosols, sea spray and volcanic aerosols. For the present day, global TP emissions are calculated to be roughly 1.33 Tg-P yr-1, with the mineral sources contributing more than 80 % to these emissions. The P solubilization from mineral dust under acidic atmospheric conditions is also parameterized in the model and is calculated to contribute about one-third (0.14 Tg-P yr-1) of the global DP atmospheric source. To our knowledge, a unique aspect of our global study is the explicit modeling of the evolution of phosphorus speciation in the atmosphere. The simulated present-day global annual DP deposition flux is 0.45 Tg-P yr-1 (about 40 % over oceans), showing a strong spatial and temporal variability. Present-day simulations of atmospheric P aerosol concentrations and deposition fluxes are satisfactory compared with available observations, indicating however an underestimate of about 70 % on current knowledge of the sources that drive the P atmospheric cycle. Sensitivity simulations using preindustrial (year 1850) anthropogenic and biomass burning emission scenarios showed a present-day increase of 75 % in the P solubilization flux from mineral dust, i.e., the rate at which P is converted into soluble forms, compared to preindustrial times, due to increasing atmospheric acidity over the last 150 years. Future reductions in air pollutants due to the implementation of air-quality regulations are expected to decrease the P solubilization flux from mineral dust by about 30 % in the year 2100 compared to the present day. Considering, however, that all the P contained in bioaerosols is readily available for uptake by marine organisms, and also accounting for all other DP sources, a total

Carbon balance variability in the Amazon Basin with climate change based on regular atmospheric profiling of greenhouse gases

Science.gov (United States)

Gatti, L.; Domingues, L. G.; Gloor, M.; Miller, J. B.; Peters, W.; Silva, M. G.; Correia, C. S. D. C.; Basso, L. S.; Alden, C. B.; Borges, V. F.; Marani, L.; Santos, R. S.; Crispim, S. P.; Sanches, A.; Costa, W. R.

2017-12-01

Net carbon exchange between tropical land and the atmosphere is potentially important because the vast amounts of carbon in forests and soils can be released on short time-scales e.g. via deforestation or changes in temperature and precipitation. Such changes may thus cause feedbacks on global climate as have been predicted in earth system models. The Amazon is the most significant region in the global carbon cycle, hosting by far the largest carbon vegetation and soil carbon pools ( 200 PgC). From 2010 onwards we have extended an earlier greenhouse gas measurement program to include regular vertical profiles of CO2 from the ground up to 4.5 km height at four sites along the main air-stream over the Amazon Basin. Our measurements demonstrate that surface flux signals are primarily concentrated to the lower 2 km and thus vertical profile measurements are ideally suited to estimate greenhouse gas balances. To understand the role of Amazon in global carbon budget it is important to maintain a long period of measurements that can represent the whole region. Our results already permit a range of insights about the magnitude, seasonality, inter-annual variation of carbon fluxes and their climate controls. Most recent years have been anomalously hot with the southern part of the Basin having warmed the most. Precipitation regimes also seem to have shifted with an increase in extreme floods. For the specific period we will discuss the period of 2010 to 2016, where the years 2010 and 2015/16 were anomalously dry and hot (both El Nino years) and the year 2013 was the wettest and coldest year. This period provides an interesting contrast of climatic conditions in a warming world with increasing human pressures and we will present the carbon balance for the basin during the last 7 years. We will analyze the effect of this climate variability on annual and seasonal carbon balances for these seven years using our atmospheric data. Our data permit us not only to estimate net CO2

Global atmospheric particle formation from CERN CLOUD measurements

CERN Document Server

Dunne, E M; Kurten, A; Almeida, J; Duplissy, J; Williamson, C; Ortega, I K; Pringle, K J; Adamov, A; Baltensperger, U; Barmet, P; Benduhn, F; Bianchi, F; Breitenlechner, M; Clarke, A; Curtius, J; Dommen, J; Donahue, N M; Ehrhart, S; Flagan, R C; Franchin, A; Guida, R; Hakala, J; Hansel, A; Heinritzi, M; Jokinen, T; Kangasluoma, J; Kirkby, J; Kulmala, M; Kupc, A; Lawler, M J; Lehtipalo, K; Makhmutov, V; Mann, G; Mathot, S; Merikanto, J; Miettinen, P; Nenes, A; Onnela, A; Rap, A; Reddington, C L S; Riccobono, F; Richards, N A D; Rissanen, M P; Rondo, L; Sarnela, N; Schobesberger, S; Sengupta, K; Simon, M; Sipila, M; Smith, J N; Stozkhov, Y; Tome, A; Trostl, J; Wagner, P E; Wimmer, D; Winkler, P M; Worsnop, D R; Carslaw, K S

2016-01-01

Fundamental questions remain about the origin of newly formed atmospheric aerosol particles because data from laboratory measurements have been insufficient to build global models. In contrast, gas-phase chemistry models have been based on laboratory kinetics measurements for decades. Here we build a global model of aerosol formation using extensive laboratory-measured nucleation rates involving sulfuric acid, ammonia, ions and organic compounds. The simulations and a comparison with atmospheric observations show that nearly all nucleation throughout the present-day atmosphere involves ammonia or biogenic organic compounds in addition to sulfuric acid. A significant fraction of nucleation involves ions, but the relatively weak dependence on ion concentrations indicates that for the processes studied variations in cosmic ray intensity do not significantly affect climate via nucleation in the present-day atmosphere.

Global biomass burning. Atmospheric, climatic, and biospheric implications

International Nuclear Information System (INIS)

Levine, J.S.

1991-01-01

Biomass burning is a significant source of atmospheric gases and, as such, may contribute to global climate changes. Biomass burning includes burning forests and savanna grasslands for land clearing, burning agricultural stubble and waste after harvesting, and burning biomass fuels. The chapters in this volume include the following topics: remote sensing of biomass burning from space;geographical distribution of burning; combustion products of burning in tropical, temperate and boreal ecosystems; burning as a global source of atmospheric gases and particulates; impacts of biomass burning gases and particulates on global climate; and the role of biomass burning on biodiversity and past global extinctions. A total of 1428 references are cited for the 63 chapters. Individual chapters are indexed separately for the data bases

Forest atmosphere carbon transfer and storage (FACTS-II) the aspen Free-air CO2 and O3 Enrichment (FACE) project: an overview.

Science.gov (United States)

R.E. Dickson; K.F. Lewin; J.G. Isebrands; M.D. Coleman; W.E. Heilman; D.E. Riemenschneider; J. Sober; G.E. Host; D.R. Zak; G.R. Hendrey; K.S. Pregitzer; D.F. Karnosky

2000-01-01

This publication briefly reviews the impact of increasing atmospheric carbon dioxide and tropospheric ozone on global climate change, and the response of forest trees to these atmospheric pollutants and their interactions; points out the need for large-scale field experiments to evaluate the response of plants to these environmental stresses; and describes the...

Long-Term, Autonomous Measurement of Atmospheric Carbon Dioxide Using an Ormosil Nanocomposite-Based Optical Sensor

Energy Technology Data Exchange (ETDEWEB)

Kisholoy Goswami

2005-10-11

The goal of this project is to construct a prototype carbon dioxide sensor that can be commercialized to offer a low-cost, autonomous instrument for long-term, unattended measurements. Currently, a cost-effective CO2 sensor system is not available that can perform cross-platform measurements (ground-based or airborne platforms such as balloon and unmanned aerial vehicle (UAV)) for understanding the carbon sequestration phenomenon. The CO2 sensor would support the research objectives of DOE-sponsored programs such as AmeriFlux and the North American Carbon Program (NACP). Global energy consumption is projected to rise 60% over the next 20 years and use of oil is projected to increase by approximately 40%. The combustion of coal, oil, and natural gas has increased carbon emissions globally from 1.6 billion tons in 1950 to 6.3 billion tons in 2000. This figure is expected to reach 10 billon tons by 2020. It is important to understand the fate of this excess CO2 in the global carbon cycle. The overall goal of the project is to develop an accurate and reliable optical sensor for monitoring carbon dioxide autonomously at least for one year at a point remote from the actual CO2 release site. In Phase I of this project, InnoSense LLC (ISL) demonstrated the feasibility of an ormosil-monolith based Autonomous Sensor for Atmospheric CO2 (ASAC) device. All of the Phase I objectives were successfully met.

Global Modeling Study of the Bioavailable Atmospheric Iron Supply to the Global Ocean

Science.gov (United States)

Myriokefalitakis, S.; Krol, M. C.; van Noije, T.; Le Sager, P.

2017-12-01

Atmospheric deposition of trace constituents acts as a nutrient source to the open ocean and affect marine ecosystem. Dust is known as a major source of nutrients to the global ocean, but only a fraction of these nutrients is released in a bioavailable form that can be assimilated by the marine biota. Iron (Fe) is a key micronutrient that significantly modulates gross primary production in the High-Nutrient-Low-Chlorophyll (HNLC) oceans, where macronutrients like nitrate are abundant, but primary production is limited by Fe scarcity. The global atmospheric Fe cycle is here parameterized in the state-of-the-art global Earth System Model EC-Earth. The model takes into account the primary emissions of both insoluble and soluble Fe forms, associated with mineral dust and combustion aerosols. The impact of atmospheric acidity and organic ligands on mineral dissolution processes, is parameterized based on updated experimental and theoretical findings. Model results are also evaluated against available observations. Overall, the link between the labile Fe atmospheric deposition and atmospheric composition changes is here demonstrated and quantified. This work has been financed by the Marie-Curie H2020-MSCA-IF-2015 grant (ID 705652) ODEON (Online DEposition over OceaNs; modeling the effect of air pollution on ocean bio-geochemistry in an Earth System Model).

Coupling of magnetospheric electrical effects into the global atmospheric electrical circuit

International Nuclear Information System (INIS)

Hays, P.B.; Roble, R.G.

1979-01-01

A quasi-static model of global atmospheric electricity has been constructed (Hays and Roble, 1978) to study the electrical processes in the lower atmosphere and the coupling between solar- and upper- atmosphere-induced variations superimposed upon the global electrical circuit. The paper reviews the essential features of this model and discusses the results obtained thus far on the effects of magnetospheric convection and substorms on the global atmospheric electrical circuit. A schematic diagram of the global quasi-static model is given. It is assumed that thunderstorms act as dipole generators, each with a positive center at the top of the cloud and a negative center a few kilometers lower than the positive center

Ions in carbon dioxide at an atmospheric pressure

International Nuclear Information System (INIS)

Ikezoe, Yasumasa; Onuki, Kaoru; Shimizu, Saburo; Nakajima, Hayato; Sato, Shoichi; Matsuoka, Shingo; Nakamura, Hirone; Tamura, Takaaki

1985-01-01

The formation and the subsequent reactions of positive and negative ions were observed by a time resolved atmospheric pressure ionization mass spectrometer (TRAPI) in an atmospheric pressure carbon dioxide added with small amounts of carbon monoxide and oxygen. A relatively stable ion of (44 x n) + (n >= 2) having a different reactivity from that of (CO 2 ) + sub(n) was found to be one of major ionic species in this gas system. This species was tentatively assigned as [O 2 (CO) 2 ] + (CO 2 )sub(n-2). A new reaction sequence of positive ions is proposed which can be operative in the radiolysis of carbon dioxide at 1 atm. (author)

Satellite observations of tropospheric ammonia and carbon monoxide: Global distributions, regional correlations and comparisons to model simulations

Science.gov (United States)

Ammonia (NH3) and carbon monoxide (CO) are primary pollutants emitted to the Earth's atmosphere from common as well as distinct sources associated with anthropogenic and natural activities. The seasonal and global distributions and correlations of NH3 and CO from the Tropospheric...

Ecosystem-atmosphere exchange of carbon in a heathland under future climatic conditions

DEFF Research Database (Denmark)

Selsted, Merete Bang

on ecosystem-atmosphere exchange of carbon in a heathland under future climatic conditions, shows that extended summer drought in combination with elevated temperature will ensure permanent dryer soil conditions, which decreases carbon turnover, while elevated atmospheric CO2 concentrations will increase...... carbon turnover. In the full future climate scenario, carbon turnover is over all expected to increase and the heathland to become a source of atmospheric CO2. The methodology of static chamber CO2 flux measurements and applying the technology in a FACE (free air CO2 enrichment) facility is a challenge...... on the atmospheric CO2 concentration. Photosynthesis and respiration run in parallel during measurements of net ecosystem exchange, and these measurements should therefore be performed with care to both the atmospheric CO2 concentration and the CO2 soil-atmosphere gradient....

Testing the performance of a Dynamic Global Ecosystem Model: Water balance, carbon balance, and vegetation structure

Science.gov (United States)

Kucharik, Christopher J.; Foley, Jonathan A.; Delire, Christine; Fisher, Veronica A.; Coe, Michael T.; Lenters, John D.; Young-Molling, Christine; Ramankutty, Navin; Norman, John M.; Gower, Stith T.

2000-09-01

While a new class of Dynamic Global Ecosystem Models (DGEMs) has emerged in the past few years as an important tool for describing global biogeochemical cycles and atmosphere-biosphere interactions, these models are still largely untested. Here we analyze the behavior of a new DGEM and compare the results to global-scale observations of water balance, carbon balance, and vegetation structure. In this study, we use version 2 of the Integrated Biosphere Simulator (IBIS), which includes several major improvements and additions to the prototype model developed by Foley et al. [1996]. IBIS is designed to be a comprehensive model of the terrestrial biosphere; the model represents a wide range of processes, including land surface physics, canopy physiology, plant phenology, vegetation dynamics and competition, and carbon and nutrient cycling. The model generates global simulations of the surface water balance (e.g., runoff), the terrestrial carbon balance (e.g., net primary production, net ecosystem exchange, soil carbon, aboveground and belowground litter, and soil CO2 fluxes), and vegetation structure (e.g., biomass, leaf area index, and vegetation composition). In order to test the performance of the model, we have assembled a wide range of continental and global-scale data, including measurements of river discharge, net primary production, vegetation structure, root biomass, soil carbon, litter carbon, and soil CO2 flux. Using these field data and model results for the contemporary biosphere (1965-1994), our evaluation shows that simulated patterns of runoff, NPP, biomass, leaf area index, soil carbon, and total soil CO2 flux agree reasonably well with measurements that have been compiled from numerous ecosystems. These results also compare favorably to other global model results.

Quantifying the Effects of Historical Land Cover Conversion Uncertainty on Global Carbon and Climate Estimates

Science.gov (United States)

Di Vittorio, A. V.; Mao, J.; Shi, X.; Chini, L.; Hurtt, G.; Collins, W. D.

2018-01-01

Previous studies have examined land use change as a driver of global change, but the translation of land use change into land cover conversion has been largely unconstrained. Here we quantify the effects of land cover conversion uncertainty on the global carbon and climate system using the integrated Earth System Model. Our experiments use identical land use change data and vary land cover conversions to quantify associated uncertainty in carbon and climate estimates. Land cover conversion uncertainty is large, constitutes a 5 ppmv range in estimated atmospheric CO2 in 2004, and generates carbon uncertainty that is equivalent to 80% of the net effects of CO2 and climate and 124% of the effects of nitrogen deposition during 1850-2004. Additionally, land cover uncertainty generates differences in local surface temperature of over 1°C. We conclude that future studies addressing land use, carbon, and climate need to constrain and reduce land cover conversion uncertainties.

A simple global carbon and energy coupled cycle model for global warming simulation: sensitivity to the light saturation effect

International Nuclear Information System (INIS)

Ichii, Kazuhito; Murakami, Kazutaka; Mukai, Toshikazu; Yamaguchi, Yasushi; Ogawa, Katsuro

2003-01-01

A simple Earth system model, the Four-Spheres Cycle of Energy and Mass (4-SCEM) model, has been developed to simulate global warming due to anthropogenic CO 2 emission. The model consists of the Atmosphere-Earth Heat Cycle (AEHC) model, the Four Spheres Carbon Cycle (4-SCC) model, and their feedback processes. The AEHC model is a one-dimensional radiative convective model, which includes the greenhouse effect of CO 2 and H 2 O, and one cloud layer. The 4-SCC model is a box-type carbon cycle model, which includes biospheric CO 2 fertilization, vegetation area variation, the vegetation light saturation effect and the HILDA oceanic carbon cycle model. The feedback processes between carbon cycle and climate considered in the model are temperature dependencies of water vapor content, soil decomposition and ocean surface chemistry. The future status of the global carbon cycle and climate was simulated up to the year 2100 based on the 'business as usual' (IS92a) emission scenario, followed by a linear decline in emissions to zero in the year 2200. The atmospheric CO 2 concentration reaches 645 ppmv in 2100 and a peak of 760 ppmv approximately in the year 2170, and becomes a steady state with 600 ppmv. The projected CO 2 concentration was lower than those of the past carbon cycle studies, because we included the light saturation effect of vegetation. The sensitivity analysis showed that uncertainties derived from the light saturation effect of vegetation and land use CO 2 emissions were the primary cause of uncertainties in projecting future CO 2 concentrations. The climate feedback effects showed rather small sensitivities compared with the impacts of those two effects. Satellite-based net primary production trends analyses can somewhat decrease the uncertainty in quantifying CO 2 emissions due to land use changes. On the other hand, as the estimated parameter in vegetation light saturation was poorly constrained, we have to quantify and constrain the effect more

'Carbon-Money Exchange' to contain global warming and deforestation

Energy Technology Data Exchange (ETDEWEB)

Nagase, Kozo E-mail: nagase@de.mbn.or.jp

2005-07-01

This paper builds a basic theory of 'Carbon-Money Exchange' in which carbon as currency in nature's household (ecosystems) and money as currency in humankind's household (economy) are exchanged just like in a foreign exchange. The simple chemical equation below makes it possible (CO{sub 2}{yields}C+O{sub 2}=C+O{sub 2}{yields}CO{sub 2}). The left-hand side represents the work of plants to remove atmospheric CO{sub 2}. The right-hand side represents the work of humans as fossil fuel consumers to produce it. The exchange of the two currencies is possible by copying the fossil fuel market. The paper concludes that this new exchange can automatically contain global warming and deforestation, replacing onerous emissions trading. Moreover, it could revolutionize the conventional economy, creating counter-capitalism, or 'carbonism'.

Top-of-atmosphere radiative forcing affected by brown carbon in the upper troposphere

Science.gov (United States)

Zhang, Yuzhong; Forrister, Haviland; Liu, Jiumeng; Dibb, Jack; Anderson, Bruce; Schwarz, Joshua P.; Perring, Anne E.; Jimenez, Jose L.; Campuzano-Jost, Pedro; Wang, Yuhang; Nenes, Athanasios; Weber, Rodney J.

2017-07-01

Carbonaceous aerosols affect the global radiative balance by absorbing and scattering radiation, which leads to warming or cooling of the atmosphere, respectively. Black carbon is the main light-absorbing component. A portion of the organic aerosol known as brown carbon also absorbs light. The climate sensitivity to absorbing aerosols rapidly increases with altitude, but brown carbon measurements are limited in the upper troposphere. Here we present aircraft observations of vertical aerosol distributions over the continental United States in May and June 2012 to show that light-absorbing brown carbon is prevalent in the troposphere, and absorbs more short-wavelength radiation than black carbon at altitudes between 5 and 12 km. We find that brown carbon is transported to these altitudes by deep convection, and that in-cloud heterogeneous processing may produce brown carbon. Radiative transfer calculations suggest that brown carbon accounts for about 24% of combined black and brown carbon warming effect at the tropopause. Roughly two-thirds of the estimated brown carbon forcing occurs above 5 km, although most brown carbon is found below 5 km. The highest radiative absorption occurred during an event that ingested a wildfire plume. We conclude that high-altitude brown carbon from biomass burning is an unappreciated component of climate forcing.

Drought sensitivity of Amazonian carbon balance revealed by atmospheric measurements

Science.gov (United States)

Gatti, L. V.; Gloor, M.; Miller, J. B.; Doughty, C. E.; Malhi, Y.; Domingues, L. G.; Basso, L. S.; Martinewski, A.; Correia, C. S. C.; Borges, V. F.; Freitas, S.; Braz, R.; Anderson, L. O.; Rocha, H.; Grace, J.; Phillips, O. L.; Lloyd, J.

2014-02-01

Feedbacks between land carbon pools and climate provide one of the largest sources of uncertainty in our predictions of global climate. Estimates of the sensitivity of the terrestrial carbon budget to climate anomalies in the tropics and the identification of the mechanisms responsible for feedback effects remain uncertain. The Amazon basin stores a vast amount of carbon, and has experienced increasingly higher temperatures and more frequent floods and droughts over the past two decades. Here we report seasonal and annual carbon balances across the Amazon basin, based on carbon dioxide and carbon monoxide measurements for the anomalously dry and wet years 2010 and 2011, respectively. We find that the Amazon basin lost 0.48+/-0.18 petagrams of carbon per year (PgCyr-1) during the dry year but was carbon neutral (0.06+/-0.1PgCyr-1) during the wet year. Taking into account carbon losses from fire by using carbon monoxide measurements, we derived the basin net biome exchange (that is, the carbon flux between the non-burned forest and the atmosphere) revealing that during the dry year, vegetation was carbon neutral. During the wet year, vegetation was a net carbon sink of 0.25+/-0.14PgCyr-1, which is roughly consistent with the mean long-term intact-forest biomass sink of 0.39+/-0.10PgCyr-1 previously estimated from forest censuses. Observations from Amazonian forest plots suggest the suppression of photosynthesis during drought as the primary cause for the 2010 sink neutralization. Overall, our results suggest that moisture has an important role in determining the Amazonian carbon balance. If the recent trend of increasing precipitation extremes persists, the Amazon may become an increasing carbon source as a result of both emissions from fires and the suppression of net biome exchange by drought.

An audit of the global carbon budget: identifying and reducing sources of uncertainty

Science.gov (United States)

Ballantyne, A. P.; Tans, P. P.; Marland, G.; Stocker, B. D.

2012-12-01

Uncertainties in our carbon accounting practices may limit our ability to objectively verify emission reductions on regional scales. Furthermore uncertainties in the global C budget must be reduced to benchmark Earth System Models that incorporate carbon-climate interactions. Here we present an audit of the global C budget where we try to identify sources of uncertainty for major terms in the global C budget. The atmospheric growth rate of CO2 has increased significantly over the last 50 years, while the uncertainty in calculating the global atmospheric growth rate has been reduced from 0.4 ppm/yr to 0.2 ppm/yr (95% confidence). Although we have greatly reduced global CO2 growth rate uncertainties, there remain regions, such as the Southern Hemisphere, Tropics and Arctic, where changes in regional sources/sinks will remain difficult to detect without additional observations. Increases in fossil fuel (FF) emissions are the primary factor driving the increase in global CO2 growth rate; however, our confidence in FF emission estimates has actually gone down. Based on a comparison of multiple estimates, FF emissions have increased from 2.45 ± 0.12 PgC/yr in 1959 to 9.40 ± 0.66 PgC/yr in 2010. Major sources of increasing FF emission uncertainty are increased emissions from emerging economies, such as China and India, as well as subtle differences in accounting practices. Lastly, we evaluate emission estimates from Land Use Change (LUC). Although relative errors in emission estimates from LUC are quite high (2 sigma ~ 50%), LUC emissions have remained fairly constant in recent decades. We evaluate the three commonly used approaches to estimating LUC emissions- Bookkeeping, Satellite Imagery, and Model Simulations- to identify their main sources of error and their ability to detect net emissions from LUC.; Uncertainties in Fossil Fuel Emissions over the last 50 years.

White dwarf stars with carbon atmospheres.

Science.gov (United States)

Dufour, P; Liebert, J; Fontaine, G; Behara, N

2007-11-22

White dwarfs represent the endpoint of stellar evolution for stars with initial masses between approximately 0.07 and 8-10, where is the mass of the Sun (more massive stars end their life as either black holes or neutron stars). The theory of stellar evolution predicts that the majority of white dwarfs have a core made of carbon and oxygen, which itself is surrounded by a helium layer and, for approximately 80 per cent of known white dwarfs, by an additional hydrogen layer. All white dwarfs therefore have been traditionally found to belong to one of two categories: those with a hydrogen-rich atmosphere (the DA spectral type) and those with a helium-rich atmosphere (the non-DAs). Here we report the discovery of several white dwarfs with atmospheres primarily composed of carbon, with little or no trace of hydrogen or helium. Our analysis shows that the atmospheric parameters found for these stars do not fit satisfactorily in any of the currently known theories of post-asymptotic giant branch evolution, although these objects might be the cooler counterpart of the unique and extensively studied PG 1159 star H1504+65 (refs 4-7). These stars, together with H1504+65, might accordingly form a new evolutionary sequence that follows the asymptotic giant branch.

Thermal Band Atmospheric Correction Using Atmospheric Profiles Derived from Global Positioning System Radio Occultation and the Atmospheric Infrared Sounder

Science.gov (United States)

Pagnutti, Mary; Holekamp, Kara; Stewart, Randy; Vaughan, Ronald D.

2006-01-01

This Rapid Prototyping Capability study explores the potential to use atmospheric profiles derived from GPS (Global Positioning System) radio occultation measurements and by AIRS (Atmospheric Infrared Sounder) onboard the Aqua satellite to improve surface temperature retrieval from remotely sensed thermal imagery. This study demonstrates an example of a cross-cutting decision support technology whereby NASA data or models are shown to improve a wide number of observation systems or models. The ability to use one data source to improve others will be critical to the GEOSS (Global Earth Observation System of Systems) where a large number of potentially useful systems will require auxiliary datasets as input for decision support. Atmospheric correction of thermal imagery decouples TOA radiance and separates surface emission from atmospheric emission and absorption. Surface temperature can then be estimated from the surface emission with knowledge of its emissivity. Traditionally, radiosonde sounders or atmospheric models based on radiosonde sounders, such as the NOAA (National Oceanic & Atmospheric Administration) ARL (Air Resources Laboratory) READY (Real-time Environmental Application and Display sYstem), provide the atmospheric profiles required to perform atmospheric correction. Unfortunately, these types of data are too spatially sparse and too infrequently taken. The advent of high accuracy, global coverage, atmospheric data using GPS radio occultation and AIRS may provide a new avenue for filling data input gaps. In this study, AIRS and GPS radio occultation derived atmospheric profiles from the German Aerospace Center CHAMP (CHAllenging Minisatellite Payload), the Argentinean Commission on Space Activities SAC-C (Satellite de Aplicaciones Cientificas-C), and the pair of NASA GRACE (Gravity Recovery and Climate Experiment) satellites are used as input data in atmospheric radiative transport modeling based on the MODTRAN (MODerate resolution atmospheric

Optimization of the sintering atmosphere for high-density hydroxyapatite–carbon nanotube composites

Science.gov (United States)

White, Ashley A.; Kinloch, Ian A.; Windle, Alan H.; Best, Serena M.

2010-01-01

Hydroxyapatite–carbon nanotube (HA–CNT) composites have the potential for improved mechanical properties over HA for use in bone graft applications. Finding an appropriate sintering atmosphere for this composite presents a dilemma, as HA requires water in the sintering atmosphere to remain phase pure and well hydroxylated, yet CNTs oxidize at the high temperatures required for sintering. The purpose of this study was to optimize the atmosphere for sintering these composites. While the reaction between carbon and water to form carbon monoxide and hydrogen at high temperatures (known as the ‘water–gas reaction’) would seem to present a problem for sintering these composites, Le Chatelier's principle suggests this reaction can be suppressed by increasing the concentration of carbon monoxide and hydrogen relative to the concentration of carbon and water, so as to retain the CNTs and keep the HA's structure intact. Eight sintering atmospheres were investigated, including standard atmospheres (such as air and wet Ar), as well as atmospheres based on the water–gas reaction. It was found that sintering in an atmosphere of carbon monoxide and hydrogen, with a small amount of water added, resulted in an optimal combination of phase purity, hydroxylation, CNT retention and density. PMID:20573629

Global atmospheric particle formation from CERN CLOUD measurements.

Science.gov (United States)

Dunne, Eimear M; Gordon, Hamish; Kürten, Andreas; Almeida, João; Duplissy, Jonathan; Williamson, Christina; Ortega, Ismael K; Pringle, Kirsty J; Adamov, Alexey; Baltensperger, Urs; Barmet, Peter; Benduhn, Francois; Bianchi, Federico; Breitenlechner, Martin; Clarke, Antony; Curtius, Joachim; Dommen, Josef; Donahue, Neil M; Ehrhart, Sebastian; Flagan, Richard C; Franchin, Alessandro; Guida, Roberto; Hakala, Jani; Hansel, Armin; Heinritzi, Martin; Jokinen, Tuija; Kangasluoma, Juha; Kirkby, Jasper; Kulmala, Markku; Kupc, Agnieszka; Lawler, Michael J; Lehtipalo, Katrianne; Makhmutov, Vladimir; Mann, Graham; Mathot, Serge; Merikanto, Joonas; Miettinen, Pasi; Nenes, Athanasios; Onnela, Antti; Rap, Alexandru; Reddington, Carly L S; Riccobono, Francesco; Richards, Nigel A D; Rissanen, Matti P; Rondo, Linda; Sarnela, Nina; Schobesberger, Siegfried; Sengupta, Kamalika; Simon, Mario; Sipilä, Mikko; Smith, James N; Stozkhov, Yuri; Tomé, Antonio; Tröstl, Jasmin; Wagner, Paul E; Wimmer, Daniela; Winkler, Paul M; Worsnop, Douglas R; Carslaw, Kenneth S

2016-12-02

Fundamental questions remain about the origin of newly formed atmospheric aerosol particles because data from laboratory measurements have been insufficient to build global models. In contrast, gas-phase chemistry models have been based on laboratory kinetics measurements for decades. We built a global model of aerosol formation by using extensive laboratory measurements of rates of nucleation involving sulfuric acid, ammonia, ions, and organic compounds conducted in the CERN CLOUD (Cosmics Leaving Outdoor Droplets) chamber. The simulations and a comparison with atmospheric observations show that nearly all nucleation throughout the present-day atmosphere involves ammonia or biogenic organic compounds, in addition to sulfuric acid. A considerable fraction of nucleation involves ions, but the relatively weak dependence on ion concentrations indicates that for the processes studied, variations in cosmic ray intensity do not appreciably affect climate through nucleation in the present-day atmosphere. Copyright © 2016, American Association for the Advancement of Science.

Towards a global understanding of vertical soil carbon dynamics: meta-analysis of soil 14C data

Science.gov (United States)

hatte, C.; Balesdent, J.; Guiot, J.

2012-12-01

Soil represents the largest terrestrial storage mechanism for atmospheric carbon from photosynthesis, with estimates ranging from 1600 Pg C within the top 1 meter to 2350 Pg C for the top 3 meters. These values are at least 2.5 times greater than atmospheric C pools. Small changes in soil organic carbon storage could result in feedback to atmospheric CO2 and the sensitivity of soil organic matter to changes in temperature, and precipitation remains a critical area of research with respect to the global carbon cycle. As an intermediate storage mechanism for organic material through time, the vertical profile of carbon generally shows an age continuum with depth. Radiocarbon provides critical information for understanding carbon exchanges between soils and atmosphere, and within soil layers. Natural and "bomb" radiocarbon has been used to demonstrate the importance and nature of the soil carbon response to climatic and human impacts on decadal to millennial timescales. Radiocarbon signatures of bulk, or chemically or physically fractionated soil, or even of specific organic compounds, offer one of the only ways to infer terrestrial carbon turnover times or test ecosystem carbon models. We compiled data from the literature on radiocarbon distribution on soil profiles and characterized each study according to the following categories: soil type, analyzed organic fraction, location (latitude, longitude, elevation), climate (temperature, precipitation), land use and sampling year. Based on the compiled data, soil carbon 14C profiles were reconstructed for each of the 226 sites. We report here partial results obtained by statistical analyses of portion of this database, i.e. bulk and bulk-like organic matter and sampling year posterior to 1980. We highlight here 14C vertical pattern in relationship with external parameters (climate, location and land use).

The global distribution of leaf chlorophyll content and seasonal controls on carbon uptake

Science.gov (United States)

Croft, H.; Chen, J. M.; Luo, X.; Bartlett, P. A.; Staebler, R. M.; He, L.; Mo, G.; Luo, S.; Simic, A.; Arabian, J.; He, Y.; Zhang, Y.; Beringer, J.; Hutley, L. B.; Noland, T. L.; Arellano, P.; Stahl, C.; Homolová, L.; Bonal, D.; Malenovský, Z.; Yi, Q.; Amiri, R.

2017-12-01

Leaf chlorophyll (ChlLeaf) is crucial to biosphere-atmosphere exchanges of carbon and water, and the functioning of terrestrial ecosystems. Improving the accuracy of modelled photosynthetic carbon uptake is a central priority for understanding ecosystem response to a changing climate. A source of uncertainty within gross primary productivity (GPP) estimates is the failure to explicitly consider seasonal controls on leaf photosynthetic potential. Whilst the inclusion of ChlLeafinto carbon models has shown potential to provide a physiological constraint, progress has been hampered by the absence of a spatially-gridded, global chlorophyll product. Here, we present the first spatially-continuous, global view of terrestrial ChlLeaf, at weekly intervals. Satellite-derived ChlLeaf was modelled using a physically-based radiative transfer modelling approach, with a two stage model inversion method. 4-Scale and SAIL canopy models were first used to model leaf-level reflectance from ENIVSAT MERIS 300m satellite data. The PROSPECT leaf model was then used to derive ChlLeaf from the modelled leaf reflectance. This algorithm was validated using measured ChlLeaf data from 248 measurements within 26 field locations, covering six plant functional types (PFTs). Modelled results show very good relationships with measured data, particularly for deciduous broadleaf forests (R2 = 0.67; pmake an important step towards improving the accuracy of global carbon budgets.

A Southern Hemisphere atmospheric history of carbon monoxide from South Pole firn air

Science.gov (United States)

Verhulst, K. R.; Aydin, M.; Novelli, P. C.; Holmes, C. D.; Prather, M. J.; Saltzman, E. S.

2013-12-01

Carbon monoxide (CO) is a reactive trace gas and is important to tropospheric photochemistry as a major sink of hydroxyl radicals (OH). Major sources of CO are fossil fuel combustion, linked mostly to automotive emissions, biomass burning, and oxidation of atmospheric methane. Understanding changes in carbon monoxide over the past century will improve our understanding of man's influence on the reactivity of the atmosphere. Little observational information is available about CO levels and emissions prior to the 1990s, particularly for the Southern Hemisphere. The NOAA global flask network provides the most complete instrumental record of CO, extending back to 1988. Annually averaged surface flask measurements suggest atmospheric CO levels at South Pole were relatively stable from 2004-2009 at about 51 nmol mol-1 [Novelli and Masarie, 2013]. In this study, a 20th century atmospheric history of CO is reconstructed from South Pole firn air measurements, using a 1-D firn air diffusion model. Firn air samples were collected in glass flasks from two adjacent holes drilled from the surface to 118 m at South Pole, Antarctica during the 2008/2009 field season and CO analysis was carried out by NOAA/CCG. Carbon monoxide levels increase from about 45 nmol mol-1 in the deepest firn sample at 116 m to 52 nmol mol-1 at 107 m, and remain constant at about 51-52 nmol mol-1 at shallower depths. Atmospheric histories based on the firn air reconstructions suggest that CO levels over Antarctica increased by roughly 40% (from about 36 to 50 nmol mol-1) between 1930-1990, at a rate of about 0.18 nmol mol-1 yr-1. Firn air and surface air results suggest the rate of CO increase at South Pole slowed considerably after 1990. The firn air-based atmospheric history is used to infer changes in Southern Hemisphere CO emissions over the 20th century.

A Miniaturized Laser Heterodyne Radiometer for a Global Ground-Based Column Carbon Monitoring Network

Science.gov (United States)

Wilson, Emily L.; Melroy, Hilary R.; Miller, J. Houston; McLinden, Matthew L.; Ott, Lesley E.; Holben, Brent

2012-01-01

We present progress in the development of a passive, miniaturized Laser Heterodyne Radiometer (mini-LHR) that will measure key greenhouse gases (C02, CH4, CO) in the atmospheric column as well as their respective altitude profiles, and O2 for a measure of atmospheric pressure. Laser heterodyne radiometry is a spectroscopic method that borrows from radio receiver technology. In this technique, a weak incoming signal containing information of interest is mixed with a stronger signal (local oscillator) at a nearby frequency. In this case, the weak signal is sunlight that has undergone absorption by a trace gas of interest and the local oscillator is a distributive feedback (DFB) laser that is tuned to a wavelength near the absorption feature of the trace gas. Mixing the sunlight with the laser light, in a fast photoreceiver, results in a beat signal in the RF. The amplitude of the beat signal tracks the concentration of the trace gas in the atmospheric column. The mini-LHR operates in tandem with AERONET, a global network of more than 450 aerosol sensing instruments. This partnership simplifies the instrument design and provides an established global network into which the mini-LHR can rapidly expand. This network offers coverage in key arctic regions (not covered by OCO-2) where accelerated warming due to the release of CO2 and CH4 from thawing tundra and permafrost is a concern as well as an uninterrupted data record that will both bridge gaps in data sets and offer validation for key flight missions such as OCO-2, OCO-3, and ASCENDS. Currently, the only ground global network that routinely measures multiple greenhouse gases in the atmospheric column is TCCON (Total Column Carbon Observing Network) with 18 operational sites worldwide and two in the US. Cost and size of TCCON installations will limit the potential for expansion, We offer a low-cost $30Klunit) solution to supplement these measurements with the added benefit of an established aerosol optical depth

Atmospheric aerosol brown carbon in the high Himalayas

Science.gov (United States)

Kirillova, Elena; Decesari, Stefano; Marinoni, Angela; Bonasoni, Paolo; Vuillermoz, Elisa; Facchini, M. Cristina; Fuzzi, Sandro

2016-04-01

Anthropogenic light-absorbing atmospheric aerosol can reach very high concentrations in the planetary boundary layer in South-East Asia ("brown clouds"), affecting atmospheric transparency and generating spatial gradients of temperature over land with a possible impact on atmospheric dynamics and monsoon circulation. Besides black carbon (BC), an important light-absorbing component of anthropogenic aerosols is the organic carbon component known as 'brown carbon' (BrC). In this research, we provided first measurements of atmospheric aerosol BrC in the high Himalayas during different seasons. Aerosol sampling was conducted at the GAW-WMO Global station "Nepal Climate Observatory-Pyramid" (NCO-P) located in the high Khumbu valley at 5079 m a.s.l. in the foothills of Mt. Everest. PM10 aerosol samples were collected from July 2013 to November 2014. The sampling strategy was set up in order to discriminate the daytime valley breeze bringing polluted air masses up to the observatory and free tropospheric air during nighttime. Water-soluble BrC (WS-BrC) and methanol-soluble BrC (MeS-BrC) were extracted and analyzed using a UV/VIS spectrophotometer equipped with a 50 cm liquid waveguide capillary cell. In the polluted air masses, the highest levels of the BrC light absorption coefficient at 365 nm (babs365) were observed during the pre-monsoon season (1.83±1.46 Mm-1 for WS-BrC and 2.86±2.49 Mm-1 for MeS-BrC) and the lowest during the monsoon season (0.21±0.22 Mm-1 for WS-BrC and 0.32±0.29 Mm-1 for MeS-BrC). The pre-monsoon season is the most frequently influenced by a strong atmospheric brown cloud (ABC) transport to NCO-P due to increased convection and mixing layer height over South Asia combined with the highest up-valley wind speed and the increase of the emissions from open fires due to the agricultural practice along the Himalayas foothills and the Indo-Gangetic Plain. In contrast, the monsoon season is characterized by a weakened valley wind regime and an

Carbon emission from global hydroelectric reservoirs revisited.

Science.gov (United States)

Li, Siyue; Zhang, Quanfa

2014-12-01

Substantial greenhouse gas (GHG) emissions from hydropower reservoirs have been of great concerns recently, yet the significant carbon emitters of drawdown area and reservoir downstream (including spillways and turbines as well as river reaches below dams) have not been included in global carbon budget. Here, we revisit GHG emission from hydropower reservoirs by considering reservoir surface area, drawdown zone and reservoir downstream. Our estimates demonstrate around 301.3 Tg carbon dioxide (CO2)/year and 18.7 Tg methane (CH4)/year from global hydroelectric reservoirs, which are much higher than recent observations. The sum of drawdown and downstream emission, which is generally overlooked, represents 42 % CO2 and 67 % CH4 of the total emissions from hydropower reservoirs. Accordingly, the global average emissions from hydropower are estimated to be 92 g CO2/kWh and 5.7 g CH4/kWh. Nonetheless, global hydroelectricity could currently reduce approximate 2,351 Tg CO2eq/year with respect to fuel fossil plant alternative. The new findings show a substantial revision of carbon emission from the global hydropower reservoirs.

The Contemporary Carbon Cycle

Science.gov (United States)

Houghton, R. A.

2003-12-01

The global carbon cycle refers to the exchanges of carbon within and between four major reservoirs: the atmosphere, the oceans, land, and fossil fuels. Carbon may be transferred from one reservoir to another in seconds (e.g., the fixation of atmospheric CO2 into sugar through photosynthesis) or over millennia (e.g., the accumulation of fossil carbon (coal, oil, gas) through deposition and diagenesis of organic matter). This chapter emphasizes the exchanges that are important over years to decades and includes those occurring over the scale of months to a few centuries. The focus will be on the years 1980-2000 but our considerations will broadly include the years ˜1850-2100. Chapter 8.09, deals with longer-term processes that involve rates of carbon exchange that are small on an annual timescale (weathering, vulcanism, sedimentation, and diagenesis).The carbon cycle is important for at least three reasons. First, carbon forms the structure of all life on the planet, making up ˜50% of the dry weight of living things. Second, the cycling of carbon approximates the flows of energy around the Earth, the metabolism of natural, human, and industrial systems. Plants transform radiant energy into chemical energy in the form of sugars, starches, and other forms of organic matter; this energy, whether in living organisms or dead organic matter, supports food chains in natural ecosystems as well as human ecosystems, not the least of which are industrial societies habituated (addicted?) to fossil forms of energy for heating, transportation, and generation of electricity. The increased use of fossil fuels has led to a third reason for interest in the carbon cycle. Carbon, in the form of carbon dioxide (CO2) and methane (CH4), forms two of the most important greenhouse gases. These gases contribute to a natural greenhouse effect that has kept the planet warm enough to evolve and support life (without the greenhouse effect the Earth's average temperature would be -33�

Dissolved organic carbon in the precipitation of Seoul, Korea: Implications for global wet depositional flux of fossil-fuel derived organic carbon

Science.gov (United States)

Yan, Ge; Kim, Guebuem

2012-11-01

Precipitation was sampled in Seoul over a one-year period from 2009 to 2010 to investigate the sources and fluxes of atmospheric dissolved organic carbon (DOC). The concentrations of DOC varied from 15 μM to 780 μM, with a volume-weighted average of 94 μM. On the basis of correlation analysis using the commonly acknowledged tracers, such as vanadium, the combustion of fossil-fuels was recognized to be the dominant source. With the aid of air mass backward trajectory analyses, we concluded that the primary fraction of DOC in our precipitation samples originated locally in Korea, albeit the frequent long-range transport from eastern and northeastern China might contribute substantially. In light of the relatively invariant organic carbon to sulfur mass ratios in precipitation over Seoul and other urban regions around the world, the global magnitude of wet depositional DOC originating from fossil-fuels was calculated to be 36 ± 10 Tg C yr-1. Our study further underscores the potentially significant environmental impacts that might be brought about by this anthropogenically derived component of organic carbon in the atmosphere.

Atmospheric pressure plasma surface modification of carbon fibres

DEFF Research Database (Denmark)

Kusano, Yukihiro; Løgstrup Andersen, Tom; Michelsen, Poul

2008-01-01

Carbon fibres are continuously treated with dielectric barrier discharge plasma at atmospheric pressure in various gas conditions for adhesion improvement in mind. An x-ray photoelectron spectroscopic analysis indicated that oxygen is effectively introduced onto the carbon fibre surfaces by He, He...

Measuring Urban Carbon Footprint from Carbon Flows in the Global Supply Chain.

Science.gov (United States)

Hu, Yuanchao; Lin, Jianyi; Cui, Shenghui; Khanna, Nina Zheng

2016-06-21

A global multiregional input-output (MRIO) model was built for eight Chinese cities to track their carbon flows. For in-depth understanding of urban carbon footprint from the perspectives of production, consumption, and trade balance, four kinds of footprints and four redefined measurement indicators were calculated. From the global supply chain, urban carbon inflows from Mainland China were larger than outflows, while the carbon outflows to European, principal North American countries and East Asia were much larger than inflows. With the rapid urbanization of China, Construction was the largest consumer and Utilities was the largest producer. Cities with higher consumption (such as Dalian, Tianjin, Shanghai, and Beijing) should change their consumption patterns, while cities with lower production efficiency (such as Dalian, Shanghai, Ningbo, and Chongqing) should improve their technology. The cities of net carbon consumption tended to transfer carbon emissions out of them by trading in carbon-intensive products, while the cities of net carbon production tended to produce carbon-intensive products for nonlocal consumers. Our results indicated that urban carbon abatement requires not only rational consumption and industrial symbiosis at the city level, but also tighter collaboration along all stages of the global supply chain.

Current sources of carbon tetrachloride (CCl4) in our atmosphere

Science.gov (United States)

Sherry, David; McCulloch, Archie; Liang, Qing; Reimann, Stefan; Newman, Paul A.

2018-02-01

Carbon tetrachloride (CCl4 or CTC) is an ozone-depleting substance whose emissive uses are controlled and practically banned by the Montreal Protocol (MP). Nevertheless, previous work estimated ongoing emissions of 35 Gg year-1 of CCl4 into the atmosphere from observation-based methods, in stark contrast to emissions estimates of 3 (0-8) Gg year-1 from reported numbers to UNEP under the MP. Here we combine information on sources from industrial production processes and legacy emissions from contaminated sites to provide an updated bottom-up estimate on current CTC global emissions of 15-25 Gg year-1. We now propose 13 Gg year-1 of global emissions from unreported non-feedstock emissions from chloromethane and perchloroethylene plants as the most significant CCl4 source. Additionally, 2 Gg year-1 are estimated as fugitive emissions from the usage of CTC as feedstock and possibly up to 10 Gg year-1 from legacy emissions and chlor-alkali plants.

Combined simulation of carbon and water isotopes in a global ocean model

Science.gov (United States)

Paul, André; Krandick, Annegret; Gebbie, Jake; Marchal, Olivier; Dutkiewicz, Stephanie; Losch, Martin; Kurahashi-Nakamura, Takasumi; Tharammal, Thejna

2013-04-01

Carbon and water isotopes are included as passive tracers in the MIT general circulation model (MITgcm). The implementation of the carbon isotopes is based on the existing MITgcm carbon cycle component and involves the fractionation processes during photosynthesis and air-sea gas exchange. Special care is given to the use of a real freshwater flux boundary condition in conjunction with the nonlinear free surface of the ocean model. The isotopic content of precipitation and water vapor is obtained from an atmospheric GCM (the NCAR CAM3) and mapped onto the MITgcm grid system, but the kinetic fractionation during evaporation is treated explicitly in the ocean model. In a number of simulations, we test the sensitivity of the carbon isotope distributions to the formulation of fractionation during photosynthesis and compare the results to modern observations of δ13C and Δ14C from GEOSECS, WOCE and CLIVAR. Similarly, we compare the resulting distribution of oxygen isotopes to modern δ18O data from the NASA GISS Global Seawater Oxygen-18 Database. The overall agreement is good, but there are discrepancies in the carbon isotope composition of the surface water and the oxygen isotope composition of the intermediate and deep waters. The combined simulation of carbon and water isotopes in a global ocean model will provide a framework for studying present and past states of ocean circulation such as postulated from deep-sea sediment records.

Boreal forests and atmosphere - Biosphere exchange of carbon dioxide

Science.gov (United States)

D'Arrigo, Rosanne; Jacoby, Gordon C.; Fung, Inez Y.

1987-01-01

Two approaches to investigating the role of boreal forests in the global carbon cycle are presented. First, a tracer support model which incorporates the normalized-difference vegetation index obtained from advanced, very high resolution radiometer radiances was used to simulate the annual cycle of CO2 in the atmosphere. Results indicate that the seasonal growth of the combined boreal forests of North America and Eurasia accounts for about 50 percent of the mean seasonal CO2 amplitude recorded at Pt. Barrow, Alaska and about 30 percent of the more globally representative CO2 signal at Mauna Loa, Hawaii. Second, tree-ring width data from four boreal treeline sites in northern Canada were positively correlated with Pt. Barrow CO2 drawdown for the period 1971-1982. These results suggest that large-scale changes in the growth of boreal forests may be contributing to the observed increasing trend in CO2 amplitude. They further suggest that tree-ring data may be applicable as indices for CO2 uptake and remote sensing estimates of photosynthetic activity.

An atmospheric perspective on North American carbon dioxide exchange: CarbonTracker

NARCIS (Netherlands)

Peters, W.; Jacobson, A.R.; Sweeney, C.; Andrews, A.E.; Conway, T.J.; Masarie, K.; Miller, J.B.; Bruhwiler, L.M.P.; Petron, G.; Hirsch, A.I.; Worthy, D.E.J.; Werf, van der G.R.; Randerson, J.T.; Wennberg, P.O.; Krol, M.C.; Tans, P.P.

2007-01-01

We present an estimate of net CO2 exchange between the terrestrial biosphere and the atmosphere across North America for every week in the period 2000 through 2005. This estimate is derived from a set of 28,000 CO2 mole fraction observations in the global atmosphere that are fed into a

Assessing carbon dioxide removal through global and regional ocean alkalinization under high and low emission pathways

Science.gov (United States)

Lenton, Andrew; Matear, Richard J.; Keller, David P.; Scott, Vivian; Vaughan, Naomi E.

2018-04-01

Atmospheric carbon dioxide (CO2) levels continue to rise, increasing the risk of severe impacts on the Earth system, and on the ecosystem services that it provides. Artificial ocean alkalinization (AOA) is capable of reducing atmospheric CO2 concentrations and surface warming and addressing ocean acidification. Here, we simulate global and regional responses to alkalinity (ALK) addition (0.25 PmolALK yr-1) over the period 2020-2100 using the CSIRO-Mk3L-COAL Earth System Model, under high (Representative Concentration Pathway 8.5; RCP8.5) and low (RCP2.6) emissions. While regionally there are large changes in alkalinity associated with locations of AOA, globally we see only a very weak dependence on where and when AOA is applied. On a global scale, while we see that under RCP2.6 the carbon uptake associated with AOA is only ˜ 60 % of the total, under RCP8.5 the relative changes in temperature are larger, as are the changes in pH (140 %) and aragonite saturation state (170 %). The simulations reveal AOA is more effective under lower emissions, therefore the higher the emissions the more AOA is required to achieve the same reduction in global warming and ocean acidification. Finally, our simulated AOA for 2020-2100 in the RCP2.6 scenario is capable of offsetting warming and ameliorating ocean acidification increases at the global scale, but with highly variable regional responses.

Atmospheric CO2 Observations Reveal Strong Correlation Between Regional Net Biospheric Carbon Uptake and Solar-Induced Chlorophyll Fluorescence

Science.gov (United States)

Shiga, Yoichi P.; Tadić, Jovan M.; Qiu, Xuemei; Yadav, Vineet; Andrews, Arlyn E.; Berry, Joseph A.; Michalak, Anna M.

2018-01-01

Recent studies have shown the promise of remotely sensed solar-induced chlorophyll fluorescence (SIF) in informing terrestrial carbon exchange, but analyses have been limited to either plot level ( 1 km2) or hemispheric/global ( 108 km2) scales due to the lack of a direct measure of carbon exchange at intermediate scales. Here we use a network of atmospheric CO2 observations over North America to explore the value of SIF for informing net ecosystem exchange (NEE) at regional scales. We find that SIF explains space-time NEE patterns at regional ( 100 km2) scales better than a variety of other vegetation and climate indicators. We further show that incorporating SIF into an atmospheric inversion leads to a spatial redistribution of NEE estimates over North America, with more uptake attributed to agricultural regions and less to needleleaf forests. Our results highlight the synergy of ground-based and spaceborne carbon cycle observations.

Solar atmosphere wave dynamics generated by solar global oscillating eigenmodes

Science.gov (United States)

Griffiths, M. K.; Fedun, V.; Erdélyi, R.; Zheng, R.

2018-01-01

The solar atmosphere exhibits a diverse range of wave phenomena, where one of the earliest discovered was the five-minute global acoustic oscillation, also referred to as the p-mode. The analysis of wave propagation in the solar atmosphere may be used as a diagnostic tool to estimate accurately the physical characteristics of the Sun's atmospheric layers. In this paper, we investigate the dynamics and upward propagation of waves which are generated by the solar global eigenmodes. We report on a series of hydrodynamic simulations of a realistically stratified model of the solar atmosphere representing its lower region from the photosphere to low corona. With the objective of modelling atmospheric perturbations, propagating from the photosphere into the chromosphere, transition region and low corona, generated by the photospheric global oscillations the simulations use photospheric drivers mimicking the solar p-modes. The drivers are spatially structured harmonics across the computational box parallel to the solar surface. The drivers perturb the atmosphere at 0.5 Mm above the bottom boundary of the model and are placed coincident with the location of the temperature minimum. A combination of the VALIIIC and McWhirter solar atmospheres are used as the background equilibrium model. We report how synthetic photospheric oscillations may manifest in a magnetic field free model of the quiet Sun. To carry out the simulations, we employed the magnetohydrodynamics code, SMAUG (Sheffield MHD Accelerated Using GPUs). Our results show that the amount of energy propagating into the solar atmosphere is consistent with a model of solar global oscillations described by Taroyan and Erdélyi (2008) using the Klein-Gordon equation. The computed results indicate a power law which is compared to observations reported by Ireland et al. (2015) using data from the Solar Dynamics Observatory/Atmospheric Imaging Assembly.

Fate of Chloromethanes in the Atmospheric Environment: Implications for Human Health, Ozone Formation and Depletion, and Global Warming Impacts.

Science.gov (United States)

Tsai, Wen-Tien

2017-09-21

Among the halogenated hydrocarbons, chloromethanes (i.e., methyl chloride, CH₃Cl; methylene chloride, CH₂Cl₂; chloroform, CHCl₃; and carbon tetrachloride, CCl₄) play a vital role due to their extensive uses as solvents and chemical intermediates. This article aims to review their main chemical/physical properties and commercial/industrial uses, as well as the environment and health hazards posed by them and their toxic decomposition products. The environmental properties (including atmospheric lifetime, radiative efficiency, ozone depletion potential, global warming potential, photochemical ozone creation potential, and surface mixing ratio) of these chlorinated methanes are also reviewed. In addition, this paper further discusses their atmospheric fates and human health implications because they are apt to reside in the lower atmosphere when released into the environment. According to the atmospheric degradation mechanism, their toxic degradation products in the troposphere include hydrogen chloride (HCl), carbon monoxide (CO), chlorine (Cl₂), formyl chloride (HCOCl), carbonyl chloride (COCl₂), and hydrogen peroxide (H₂O₂). Among them, COCl₂ (also called phosgene) is a powerful irritating gas, which is easily hydrolyzed or thermally decomposed to form hydrogen chloride.

Global anthropogenic emissions of particulate matter including black carbon

Science.gov (United States)

Klimont, Zbigniew; Kupiainen, Kaarle; Heyes, Chris; Purohit, Pallav; Cofala, Janusz; Rafaj, Peter; Borken-Kleefeld, Jens; Schöpp, Wolfgang

2017-07-01

was the most important sector, contributing about 60 % for BC and OC, 45 % for PM2. 5, and less than 40 % for PM10, where large combustion sources and industrial processes are equally important. Global anthropogenic emissions of BC were estimated at about 6.6 and 7.2 Tg in 2000 and 2010, respectively, and represent about 15 % of PM2. 5 but for some sources reach nearly 50 %, i.e. for the transport sector. Our global BC numbers are higher than previously published owing primarily to the inclusion of new sources. This PM estimate fills the gap in emission data and emission source characterization required in air quality and climate modelling studies and health impact assessments at a regional and global level, as it includes both carbonaceous and non-carbonaceous constituents of primary particulate matter emissions. The developed emission dataset has been used in several regional and global atmospheric transport and climate model simulations within the ECLIPSE (Evaluating the Climate and Air Quality Impacts of Short-Lived Pollutants) project and beyond, serves better parameterization of the global integrated assessment models with respect to representation of black carbon and organic carbon emissions, and built a basis for recently published global particulate number estimates.

Global anthropogenic emissions of particulate matter including black carbon

Directory of Open Access Journals (Sweden)

Z. Klimont

2017-07-01

anthropogenic total, and residential combustion was the most important sector, contributing about 60 % for BC and OC, 45 % for PM2. 5, and less than 40 % for PM10, where large combustion sources and industrial processes are equally important. Global anthropogenic emissions of BC were estimated at about 6.6 and 7.2 Tg in 2000 and 2010, respectively, and represent about 15 % of PM2. 5 but for some sources reach nearly 50 %, i.e. for the transport sector. Our global BC numbers are higher than previously published owing primarily to the inclusion of new sources. This PM estimate fills the gap in emission data and emission source characterization required in air quality and climate modelling studies and health impact assessments at a regional and global level, as it includes both carbonaceous and non-carbonaceous constituents of primary particulate matter emissions. The developed emission dataset has been used in several regional and global atmospheric transport and climate model simulations within the ECLIPSE (Evaluating the Climate and Air Quality Impacts of Short-Lived Pollutants project and beyond, serves better parameterization of the global integrated assessment models with respect to representation of black carbon and organic carbon emissions, and built a basis for recently published global particulate number estimates.

A Study of the Abundance and 13C/12C Ratio of Atmospheric Carbon Dioxide to Advance the Scientific Understanding of Terrestrial Processes Regulating the Global Carbon Cycle

Energy Technology Data Exchange (ETDEWEB)

Stephen C. Piper

2005-10-15

The primary goal of our research program, consistent with the goals of the U.S. Climate Change Science Program and funded by the terrestrial carbon processes (TCP) program of DOE, has been to improve understanding of changes in the distribution and cycling of carbon among the active land, ocean and atmosphere reservoirs, with particular emphasis on terrestrial ecosystems. Our approach is to systematically measure atmospheric CO2 to produce time series data essential to reveal temporal and spatial patterns. Additional measurements of the 13C/12C isotopic ratio of CO2 provide a basis for distinguishing organic and inorganic processes. To pursue the significance of these patterns further, our research also involved interpretations of the observations by models, measurements of inorganic carbon in sea water, and of CO2 in air near growing land plants.

ISLSCP II GlobalView: Atmospheric Methane Concentrations

Data.gov (United States)

National Aeronautics and Space Administration — ABSTRACT: The GlobalView Methane (CH4) data product contains synchronized and smoothed time series of atmospheric CH4 concentrations at selected sites that were...

NASA/MSFC FY88 Global Scale Atmospheric Processes Research Program Review

Science.gov (United States)

Wilson, Greg S. (Editor); Leslie, Fred W. (Editor); Arnold, J. E. (Editor)

1989-01-01

Interest in environmental issues and the magnitude of the environmental changes continues. One way to gain more understanding of the atmosphere is to make measurements on a global scale from space. The Earth Observation System is a series of new sensors to measure globally atmospheric parameters. Analysis of satellite data by developing algorithms to interpret the radiance information improves the understanding and also defines requirements for these sensors. One measure of knowledge of the atmosphere lies in the ability to predict its behavior. Use of numerical and experimental models provides a better understanding of these processes. These efforts are described in the context of satellite data analysis and fundamental studies of atmospheric dynamics which examine selected processes important to the global circulation.

Global Change in the Upper Atmosphere

Czech Academy of Sciences Publication Activity Database

Laštovička, Jan; Akmaev, R. A.; Beig, G.; Bremer, J.; Emmert, J. T.

2006-01-01

Roč. 314, č. 5803 (2006), s. 1253-1254 ISSN 0036-8075 R&D Projects: GA MŠk OC 091 Institutional research plan: CEZ:AV0Z30420517 Keywords : Global change * Upper Atmosphere * Ionosphere Subject RIV: DG - Athmosphere Sciences, Meteorology Impact factor: 30.028, year: 2006

Atmospheric Chemistry in a Changing World

Science.gov (United States)

Brune, William H.

The world is changing,and the atmosphere's composition is changing with it. Human activity is responsible for much of this. Global population growth and migration to urban centers, extensive biomass burning, the spread of fertilizer-intensive agribusiness, globalization of business and industry, rising standards of living in the developing world, and increased energy use fuels atmospheric change. If current practices continue, atmospheric increases are likely for the greenhouse gases carbon dioxide, methane, nitrous oxide; and for the chemically active gases nitric oxide, sulfur dioxide,and ammonia. Increases in global tropospheric ozone and aerosols are a distinct possibility.

ISLSCP II GlobalView: Atmospheric Methane Concentrations

Data.gov (United States)

National Aeronautics and Space Administration — The GlobalView Methane (CH4) data product contains synchronized and smoothed time series of atmospheric CH4 concentrations at selected sites that were created using...

Achieving Carbon Neutrality in the Global Aluminum Industry

Science.gov (United States)

Das, Subodh

2012-02-01

In the 21st century, sustainability is widely regarded as the new corporate culture, and leading manufacturing companies (Toyota, GE, and Alcoa) and service companies (Google and Federal Express) are striving towards carbon neutrality. The current carbon footprint of the global aluminum industry is estimated at 500 million metric tonnes carbon dioxide equivalent (CO2eq), representing about 1.7% of global emissions from all sources. For the global aluminum industry, carbon neutrality is defined as a state where the total "in-use" CO2eq saved from all products in current use, including incremental process efficiency improvements, recycling, and urban mining activities, equals the CO2eq expended to produce the global output of aluminum. This paper outlines an integrated and quantifiable plan for achieving "carbon neutrality" in the global aluminum industry by advocating five actionable steps: (1) increase use of "green" electrical energy grid by 8%, (2) reduce process energy needs by 16%, (3) deploy 35% of products in "in-use" energy saving applications, (4) divert 6.1 million metric tonnes/year from landfills, and (5) mine 4.5 million metric tonnes/year from aluminum-rich "urban mines." Since it takes 20 times more energy to make aluminum from bauxite ore than to recycle it from scrap, the global aluminum industry could set a reasonable, self-imposed energy/carbon neutrality goal to incrementally increase the supply of recycled aluminum by at least 1.05 metric tonnes for every tonne of incremental production via primary aluminum smelter capacity. Furthermore, the aluminum industry can and should take a global leadership position by actively developing internationally accepted and approved carbon footprint credit protocols.

Atmospheric carbon injection linked to end-Triassic mass extinction.

Science.gov (United States)

Ruhl, Micha; Bonis, Nina R; Reichart, Gert-Jan; Sinninghe Damsté, Jaap S; Kürschner, Wolfram M

2011-07-22

The end-Triassic mass extinction (~201.4 million years ago), marked by terrestrial ecosystem turnover and up to ~50% loss in marine biodiversity, has been attributed to intensified volcanic activity during the break-up of Pangaea. Here, we present compound-specific carbon-isotope data of long-chain n-alkanes derived from waxes of land plants, showing a ~8.5 per mil negative excursion, coincident with the extinction interval. These data indicate strong carbon-13 depletion of the end-Triassic atmosphere, within only 10,000 to 20,000 years. The magnitude and rate of this carbon-cycle disruption can be explained by the injection of at least ~12 × 10(3) gigatons of isotopically depleted carbon as methane into the atmosphere. Concurrent vegetation changes reflect strong warming and an enhanced hydrological cycle. Hence, end-Triassic events are robustly linked to methane-derived massive carbon release and associated climate change.

NASA/MSFC FY90 Global Scale Atmospheric Processes Research Program Review

Science.gov (United States)

Leslie, Fred W. (Editor)

1990-01-01

Research supported by the Global Atmospheric Research Program at the Marshall Space Flight Center on atmospheric remote sensing, meteorology, numerical weather forecasting, satellite data analysis, cloud precipitation, atmospheric circulation, atmospheric models and related topics is discussed.

Impact of atmospheric and terrestrial CO2 feedbacks on fertilization-induced marine carbon uptake

Science.gov (United States)

Oschlies, A.

2009-08-01

The sensitivity of oceanic CO2 uptake to alterations in the marine biological carbon pump, such as brought about by natural or purposeful ocean fertilization, has repeatedly been investigated by studies employing numerical biogeochemical ocean models. It is shown here that the results of such ocean-centered studies are very sensitive to the assumption made about the response of the carbon reservoirs on the atmospheric side of the sea surface. Assumptions made include prescribed atmospheric pCO2, an interactive atmospheric CO2 pool exchanging carbon with the ocean but not with the terrestrial biosphere, and an interactive atmosphere that exchanges carbon with both oceanic and terrestrial carbon pools. The impact of these assumptions on simulated annual to millennial oceanic carbon uptake is investigated for a hypothetical increase in the C:N ratio of the biological pump and for an idealized enhancement of phytoplankton growth. Compared to simulations with interactive atmosphere, using prescribed atmospheric pCO2 overestimates the sensitivity of the oceanic CO2 uptake to changes in the biological pump, by about 2%, 25%, 100%, and >500% on annual, decadal, centennial, and millennial timescales, respectively. The smaller efficiency of the oceanic carbon uptake under an interactive atmosphere is due to the back flux of CO2 that occurs when atmospheric CO2 is reduced. Adding an interactive terrestrial carbon pool to the atmosphere-ocean model system has a small effect on annual timescales, but increases the simulated fertilization-induced oceanic carbon uptake by about 4%, 50%, and 100% on decadal, centennial, and millennial timescales, respectively, for pCO2 sensitivities of the terrestrial carbon storage in the middle range of the C4MIP models (Friedlingstein et al., 2006). For such sensitivities, a substantial fraction of oceanic carbon uptake induced by natural or purposeful ocean fertilization originates, on timescales longer than decades, not from the atmosphere

Bird specimens track 135 years of atmospheric black carbon and environmental policy

Science.gov (United States)

DuBay, Shane G.; Fuldner, Carl C.

2017-10-01

Atmospheric black carbon has long been recognized as a public health and environmental concern. More recently, black carbon has been identified as a major, ongoing contributor to anthropogenic climate change, thus making historical emission inventories of black carbon an essential tool for assessing past climate sensitivity and modeling future climate scenarios. Current estimates of black carbon emissions for the early industrial era have high uncertainty, however, because direct environmental sampling is sparse before the mid-1950s. Using photometric reflectance data of >1,300 bird specimens drawn from natural history collections, we track relative ambient concentrations of atmospheric black carbon between 1880 and 2015 within the US Manufacturing Belt, a region historically reliant on coal and dense with industry. Our data show that black carbon levels within the region peaked during the first decade of the 20th century. Following this peak, black carbon levels were positively correlated with coal consumption through midcentury, after which they decoupled, with black carbon concentrations declining as consumption continued to rise. The precipitous drop in atmospheric black carbon at midcentury reflects policies promoting burning efficiency and fuel transitions rather than regulating emissions alone. Our findings suggest that current emission inventories based on predictive modeling underestimate levels of atmospheric black carbon for the early industrial era, suggesting that the contribution of black carbon to past climate forcing may also be underestimated. These findings build toward a spatially dynamic emission inventory of black carbon based on direct environmental sampling.

MIPAS ESA v7 carbon tetrachloride data: distribution, trend and atmospheric lifetime estimation

Science.gov (United States)

Valeri, M.; Barbara, F.; Boone, C. D.; Ceccherini, S.; Gai, M.; Maucher, G.; Raspollini, P.; Ridolfi, M.; Sgheri, L.; Wetzel, G.; Zoppetti, N.

2017-12-01

Carbon tetrachloride (CCl4) is a strong ozone-depleting atmospheric gas regulated by the Montreal protocol. Recently it received increasing interest due to the so called "mystery of CCl4": it was found that its atmospheric concentration at the surface declines with a rate significantly smaller than its lifetime-limited rate. Indeed there is a discrepancy between atmospheric observations and the estimated distribution based on the reported production and consumption. Michelson Interferometer for Passive Atmospheric Sounding (MIPAS) measurements are used to estimate CCl4 distributions, its trend, and atmospheric lifetime in the upper troposphere / lower stratosphere (UTLS) region. In particular, here we use MIPAS product generated with Version 7 of the Level 2 algorithm operated by the European Space Agency. The CCl4 distribution shows features typical of long-lived species of anthropogenic origin: higher concentrations in the troposphere, decreasing with altitude due to the photolysis. We compare MIPAS CCl4 data with independent observations from Atmospheric Chemistry Experiment - Fourier Transform Spectrometer (ACE - FTS) and stratospheric balloon version of MIPAS (MIPAS-B). The comparison shows a general good agreement between the different datasets. CCl4 trends are evaluated as a function of both latitude and altitude: negative trends (-10/ -15 pptv/decade, -10/ -30 %/decade) are found at all latitudes in the UTLS, apart from a region in the Southern mid-latitudes between 50 and 10 hPa where the trend is slightly positive (5/10 pptv/decade, 15/20 %/decade). At the lowest altitudes sounded by the MIPAS scan we find trend values consistent with those determined on the basis of the Advanced Global Atmospheric Gases Experiment (AGAGE) and the National Oceanic and Atmospheric Administration / Earth System Research Laboratory / Halocarbons and other Atmospheric Trace Species (NOAA / ESRL / HATS) networks. CCl4 global average lifetime of 47(39 - 61) years has been

Atmospheric deposition, CO2, and change in the land carbon sink

DEFF Research Database (Denmark)

Martinez-Fernandez, Cristina; Vicca, Sara; Janssens, Ivan A.

2017-01-01

Concentrations of atmospheric carbon dioxide (CO2) have continued to increase whereas atmospheric deposition of sulphur and nitrogen has declined in Europe and the USA during recent decades. Using time series of flux observations from 23 forests distributed throughout Europe and the USA, and gene...... show the need to include the effects of changing atmospheric composition, beyond CO2, to assess future dynamics of carbon-climate feedbacks not currently considered in earth system/climate modelling....

Global low-carbon transition and China's response strategies

Directory of Open Access Journals (Sweden)

Jian-Kun He

2016-12-01

Full Text Available The Paris Agreement establishes a new mechanism for post-2020 global climate governance, and sets long-term goals for global response to climate change, which will accelerate worldwide low-carbon transformation of economic development pattern, promote the revolutionary reform of energy system, boost a fundamental change in the mode of social production and consumption, and further the civilization of human society from industrial civilization to eco-civilization. The urgency of global low-carbon transition will reshape the competition situation of world's economy, trade and technology. Taking the construction of eco-civilization as a guide, China explores green and low-carbon development paths, establishes ambitious intended nationally determined contribution (INDC targets and action plans, advances energy production and consumption revolution, and speeds up the transformation of economic development pattern. These strategies and actions not only confirm to the trend of the world low-carbon transition, but also meet the intrinsic requirements for easing the domestic resources and environment constraints and realizing sustainable development. They are multi-win-win strategies for promotion of economic development and environmental protection and mitigation of carbon emissions. China should take the global long-term emission reduction targets as a guide, and formulate medium and long-term low-carbon development strategy, build the core competitiveness of low-carbon advanced technology and development pattern, and take an in-depth part in global governance so as to reflect the responsibility of China as a great power in constructing a community of common destiny for all mankind and addressing global ecological crisis.

Problems in global atmospheric chemistry

Science.gov (United States)

Crutzen, Paul J.

1993-02-01

The chemistry of the atmosphere is substantially influenced by a wide range of chemical processes which are primarily driven by the action of ultraviolet radiation of wavelengths shorter than 320 nm (UV-B) on ozone and water vapor. This leads to the formation of hydroxyl (OH) radicals which, despite very low tropospheric concentrations, remove most gases that are emitted into the atmosphere by natural and anthropogenic processes. Therefore, although only about 10% of all atmospheric ozone is located in the troposphere, through the formation of OH, it determines the oxidation efficiency of the atmosphere and is, therefore, of the utmost importance for maintaining its chemical composition. Due to a variety of human activities, especially through increasing emissions of CH4, CO, and NOx, the concentrations of tropospheric ozone and hydroxyl are expected to be increasing in polluted and decreasing in clean tropospheric environments. Altogether, this may be leading to an overall decrease in the oxidation efficiency of the atmosphere, contributing to a gradual buildup of several longlived trace gases that are primarily removed by reaction with OH. In the stratosphere, especially due to catalytic reactions of chlorine-containing gases of industrial origin, ozone is being depleted, most drastically noted during the early spring months over Antarctica. Because ozone is the only atmospheric constituent that can significantly absorb solar radiation in the wavelength region 240 - 320 nm, this loss of ozone enhances the penetration of biologically harmful UV-B radiation to the earth's surface with ensuing negative consequences for the biosphere. Several of the aforementioned chemically active trace gases with growing trends in the atmosphere are also efficient greenhouse gases. Together they can exert a warming effect on the earth's climate about equal to that of carbon dioxide.

Increasing atmospheric carbon dioxide and its consequences

Energy Technology Data Exchange (ETDEWEB)

Lockwood, J G

1982-09-16

The effects of increasing CO/sub 2/ concentrations in the atmosphere are estimated using general circulation models (GCMs), which have the ability to portray many of the nonlinear feedback processes which serve to regulate atmospheric (and hence climatic) changes. GCMs predict that a doubling of atmospheric CO/sub 2/ would result in a 2-3 k increase of globally averaged surface air temperature. The largest warming will occur in the winter in high latitudes. Detection studies are now being directed towards isolating those parts of observed climate fluctuations that are attributable to increasing atmospheric CO/sub 2/. (KRM)

Towards a global assessment of pyrogenic carbon from vegetation fires.

Science.gov (United States)

Santín, Cristina; Doerr, Stefan H; Kane, Evan S; Masiello, Caroline A; Ohlson, Mikael; de la Rosa, Jose Maria; Preston, Caroline M; Dittmar, Thorsten

2016-01-01

The production of pyrogenic carbon (PyC; a continuum of organic carbon (C) ranging from partially charred biomass and charcoal to soot) is a widely acknowledged C sink, with the latest estimates indicating that ~50% of the PyC produced by vegetation fires potentially sequesters C over centuries. Nevertheless, the quantitative importance of PyC in the global C balance remains contentious, and therefore, PyC is rarely considered in global C cycle and climate studies. Here we examine the robustness of existing evidence and identify the main research gaps in the production, fluxes and fate of PyC from vegetation fires. Much of the previous work on PyC production has focused on selected components of total PyC generated in vegetation fires, likely leading to underestimates. We suggest that global PyC production could be in the range of 116-385 Tg C yr(-1) , that is ~0.2-0.6% of the annual terrestrial net primary production. According to our estimations, atmospheric emissions of soot/black C might be a smaller fraction of total PyC (<2%) than previously reported. Research on the fate of PyC in the environment has mainly focused on its degradation pathways, and its accumulation and resilience either in situ (surface soils) or in ultimate sinks (marine sediments). Off-site transport, transformation and PyC storage in intermediate pools are often overlooked, which could explain the fate of a substantial fraction of the PyC mobilized annually. We propose new research directions addressing gaps in the global PyC cycle to fully understand the importance of the products of burning in global C cycle dynamics. © 2015 The Authors. Global Change Biology Published by John Wiley & Sons Ltd.

Substantial global carbon uptake by cement carbonation

OpenAIRE

Xi, Fengming; Davis, Steven J.; Ciais, Philippe; Crawford-Brown, Douglas; Guan, Dabo; Pade, Claus; Shi, Tiemao; Syddall, Mark; Lv, Jie; Ji, Lanzhu; Bing, Longfei; Wang, Jiaoyue; Wei, Wei; Yang, Keun-Hyeok; Lagerblad, Björn

2016-01-01

Calcination of carbonate rocks during the manufacture of cement produced 5% of global CO2 emissions from all industrial process and fossil-fuel combustion in 20131, 2. Considerable attention has been paid to quantifying these industrial process emissions from cement production2, 3, but the natural reversal of the process—carbonation—has received little attention in carbon cycle studies. Here, we use new and existing data on cement materials during cement service life, demolition, and secondar...

The role of urbanization in the global carbon cycle

Directory of Open Access Journals (Sweden)

Galina eChurkina

2016-01-01

Full Text Available Urban areas account for more than 70% of CO2 emissions from burning fossil fuels. Urban expansion in tropics is responsible for 5% of the annual emissions from land use change. Here I show that the effect of urbanization on the global carbon cycle extends beyond these emissions. I quantify the contribution of urbanization to the major carbon fluxes and pools globally and identify gaps crucial for predicting the evolution of the carbon cycle in the future. Urban residents currently control ~22 (12-40 % of the land carbon uptake (112 PgC/yr and ~24 (15-39 % of the carbon emissions (117 PgC/yr from land globally. Urbanization resulted in the creation of new carbon pools on land such as buildings (~6.7 PgC and landfills (~30 PgC. Together these pools store 1.6 (±0.3 % of the total vegetation and soil carbon pools globally. The creation and maintenance of these new pools has been associated with high emissions of CO2, which are currently better understood than the processes associated with the dynamics of these pools and accompanying uptake of carbon. Predictions of the future trajectories of the global carbon cycle will require a much better understanding of how urban development affects the carbon cycle over the long term.

Technical Report Series on Global Modeling and Data Assimilation. Volume 31; Global Surface Ocean Carbon Estimates in a Model Forced by MERRA

Science.gov (United States)

Gregg, Watson W.; Casey, Nancy W.; Rousseaux, Cecile S.

2013-01-01

MERRA products were used to force an established ocean biogeochemical model to estimate surface carbon inventories and fluxes in the global oceans. The results were compared to public archives of in situ carbon data and estimates. The model exhibited skill for ocean dissolved inorganic carbon (DIC), partial pressure of ocean CO2 (pCO2) and air-sea fluxes (FCO2). The MERRA-forced model produced global mean differences of 0.02% (approximately 0.3 microns) for DIC, -0.3% (about -1.2 (micro) atm; model lower) for pCO2, and -2.3% (-0.003 mol C/sq m/y) for FCO2 compared to in situ estimates. Basin-scale distributions were significantly correlated with observations for all three variables (r=0.97, 0.76, and 0.73, P<0.05, respectively for DIC, pCO2, and FCO2). All major oceanographic basins were represented as sources to the atmosphere or sinks in agreement with in situ estimates. However, there were substantial basin-scale and local departures.

Ocean Fertilization for Sequestration of Carbon Dioxide from the Atmosphere

Science.gov (United States)

Boyd, Philip W.

The ocean is a major sink for both preindustrial and anthropogenic carbon dioxide. Both physically and biogeochemically driven pumps, termed the solubility and biological pump, respectively Fig.5.1) are responsible for the majority of carbon sequestration in the ocean's interior [1]. The solubility pump relies on ocean circulation - specifically the impact of cooling of the upper ocean at high latitudes both enhances the solubility of carbon dioxide and the density of the waters which sink to great depth (the so-called deepwater formation) and thereby sequester carbon in the form of dissolved inorganic carbon (Fig.5.1). The biological pump is driven by the availability of preformed plant macronutrients such as nitrate or phosphate which are taken up by phytoplankton during photosynthetic carbon fixation. A small but significant proportion of this fixed carbon sinks into the ocean's interior in the form of settling particles, and in order to maintain equilibrium carbon dioxide from the atmosphere is transferred across the air-sea interface into the ocean (the so-called carbon drawdown) thereby decreasing atmospheric carbon dioxide (Fig.5.1).Fig.5.1

The topology of non-linear global carbon dynamics: from tipping points to planetary boundaries

International Nuclear Information System (INIS)

Anderies, J M; Carpenter, S R; Steffen, Will; Rockström, Johan

2013-01-01

We present a minimal model of land use and carbon cycle dynamics and use it to explore the relationship between non-linear dynamics and planetary boundaries. Only the most basic interactions between land cover and terrestrial, atmospheric, and marine carbon stocks are considered in the model. Our goal is not to predict global carbon dynamics as it occurs in the actual Earth System. Rather, we construct a conceptually reasonable heuristic model of a feedback system between different carbon stocks that captures the qualitative features of the actual Earth System and use it to explore the topology of the boundaries of what can be called a ‘safe operating space’ for humans. The model analysis illustrates the existence of dynamic, non-linear tipping points in carbon cycle dynamics and the potential complexity of planetary boundaries. Finally, we use the model to illustrate some challenges associated with navigating planetary boundaries. (letter)

The topology of non-linear global carbon dynamics: from tipping points to planetary boundaries

Science.gov (United States)

Anderies, J. M.; Carpenter, S. R.; Steffen, Will; Rockström, Johan

2013-12-01

We present a minimal model of land use and carbon cycle dynamics and use it to explore the relationship between non-linear dynamics and planetary boundaries. Only the most basic interactions between land cover and terrestrial, atmospheric, and marine carbon stocks are considered in the model. Our goal is not to predict global carbon dynamics as it occurs in the actual Earth System. Rather, we construct a conceptually reasonable heuristic model of a feedback system between different carbon stocks that captures the qualitative features of the actual Earth System and use it to explore the topology of the boundaries of what can be called a ‘safe operating space’ for humans. The model analysis illustrates the existence of dynamic, non-linear tipping points in carbon cycle dynamics and the potential complexity of planetary boundaries. Finally, we use the model to illustrate some challenges associated with navigating planetary boundaries.

Land–atmosphere feedbacks amplify aridity increase over land under global warming

Science.gov (United States)

Berg, Alexis; Findell, Kirsten; Lintner, Benjamin; Giannini, Alessandra; Seneviratne, Sonia I.; van den Hurk, Bart; Lorenz, Ruth; Pitman, Andy; Hagemann, Stefan; Meier, Arndt; Cheruy, Frédérique; Ducharne, Agnès; Malyshev, Sergey; Milly, Paul C. D.

2016-01-01

The response of the terrestrial water cycle to global warming is central to issues including water resources, agriculture and ecosystem health. Recent studies indicate that aridity, defined in terms of atmospheric supply (precipitation, P) and demand (potential evapotranspiration, Ep) of water at the land surface, will increase globally in a warmer world. Recently proposed mechanisms for this response emphasize the driving role of oceanic warming and associated atmospheric processes. Here we show that the aridity response is substantially amplified by land–atmosphere feedbacks associated with the land surface’s response to climate and CO2 change. Using simulations from the Global Land Atmosphere Coupling Experiment (GLACE)-CMIP5 experiment, we show that global aridity is enhanced by the feedbacks of projected soil moisture decrease on land surface temperature, relative humidity and precipitation. The physiological impact of increasing atmospheric CO2 on vegetation exerts a qualitatively similar control on aridity. We reconcile these findings with previously proposed mechanisms by showing that the moist enthalpy change over land is unaffected by the land hydrological response. Thus, although oceanic warming constrains the combined moisture and temperature changes over land, land hydrology modulates the partitioning of this enthalpy increase towards increased aridity.

Vulnerability of permafrost carbon to global warming. Part II: sensitivity of permafrost carbon stock to global warming

Energy Technology Data Exchange (ETDEWEB)

Khvorostyanov, D.V.; Ciais, G. (Laboratoire des Sciences du Climat et l' Environnement, Saclay (France)); Krinner, G. (Laboratoire de Glaciologie et Geophysique de l' Environnement, St Martin d' Heres (France)). e-mail: Dimitry.Khvorostiyanov@lsce.ipsl.fr; Zimov, S.A. (Northeast Science Station, Cherskii (RU)); Corradi, C. (UNITUS, Univ. of Tuscia, Veterbo (Italy)); Guggenberger, G. (Inst. of Soil Science and Plant Nutrition, Martin-Luther-Univ., Halle-Wittenberg (DE))

2008-07-01

In the companion paper (Part I), we presented a model of permafrost carbon cycle to study the sensitivity of frozen carbon stocks to future climate warming. The mobilization of deep carbon stock of the frozen Pleistocene soil in the case of rapid stepwise increase of atmospheric temperature was considered. In this work, we adapted the model to be used also for floodplain tundra sites and to account for the processes in the soil active layer. The new processes taken into account are litter input and decomposition, plant-mediated transport of methane, and leaching of exudates from plant roots. The SRES-A2 transient climate warming scenario of the IPSL CM4 climate model is used to study the carbon fluxes from the carbon-rich Pleistocene soil with seasonal active-layer carbon cycling on top of it. For a point to the southwest from the western branch of Yedoma Ice Complex, where the climate warming is strong enough to trigger self-sustainable decomposition processes, about 256 kg C/m2, or 70% of the initial soil carbon stock under present-day climate conditions, are emitted to the atmosphere in about 120 yr, including 20 kg C/m2 released as methane. The total average flux of CO{sub 2} and methane emissions to the atmosphere during this time is of 2.1 kg C/m2/yr. Within the Yedoma, whose most part of the territory remains relatively cold, the emissions are much smaller: 0.2 kg C/m2/yr between 2050 and 2100 for Yakutsk area. In a test case with saturated upper-soil meter, when the runoff is insufficient to evacuate the meltwater, 0.05 kg CH{sub 4}/m2/yr on average are emitted as methane during 250 yr starting from 2050. The latter can translate to the upper bound of 1 GtC/yr in CO{sub 2} equivalent from the 1 million km2 area of the Yedoma

Photosynthesis-dependent isoprene emission from leaf to planet in a global carbon-chemistry-climate model

OpenAIRE

Unger, N.; Harper, K.; Zheng, Y.; Kiang, N. Y.; Aleinov, I.; Arneth, A.; Schurgers, G.; Amelynyck, C.; Goldstein, A.; Guenther, A.; Heinesch, B.; Hewitt, C. N.; Karl, T.; Laffineur, Q.; Langford, B.

2013-01-01

We describe the implementation of a biochemical model of isoprene emission that depends on the electron requirement for isoprene synthesis into the Farquhar–Ball–Berry leaf model of photosynthesis and stomatal conductance that is embedded within a global chemistry-climate simulation framework. The isoprene production is calculated as a function of electron transport-limited photosynthesis, intercellular and atmospheric carbon dioxide concentration, and canopy temperature. Th...

Global Validation of MODIS Atmospheric Profile-Derived Near-Surface Air Temperature and Dew Point Estimates

Science.gov (United States)

Famiglietti, C.; Fisher, J.; Halverson, G. H.

2017-12-01

This study validates a method of remote sensing near-surface meteorology that vertically interpolates MODIS atmospheric profiles to surface pressure level. The extraction of air temperature and dew point observations at a two-meter reference height from 2001 to 2014 yields global moderate- to fine-resolution near-surface temperature distributions that are compared to geographically and temporally corresponding measurements from 114 ground meteorological stations distributed worldwide. This analysis is the first robust, large-scale validation of the MODIS-derived near-surface air temperature and dew point estimates, both of which serve as key inputs in models of energy, water, and carbon exchange between the land surface and the atmosphere. Results show strong linear correlations between remotely sensed and in-situ near-surface air temperature measurements (R2 = 0.89), as well as between dew point observations (R2 = 0.77). Performance is relatively uniform across climate zones. The extension of mean climate-wise percent errors to the entire remote sensing dataset allows for the determination of MODIS air temperature and dew point uncertainties on a global scale.

Global warming and the forest fire business in Canada

International Nuclear Information System (INIS)

Stocks, B.J.

1991-01-01

The current forest fire situation in Canada is outlined, and an attempt is made to predict the impact of global warming on the forest fire business in Canada. Despite the development of extremely sophisticated provincial and territorial fire management systems, forest fires continue to exert a tremendous influence on the Canadian forest resource. Research into the relationship between climate warming and forest fires has fallen into two categories: the effect of future global warming on fire weather severity, and the current contribution of forest fires to global atmospheric greenhouse gas budgets. A 46% increase in seasonal fire severity across Canada is suggested under a doubled atmospheric carbon dioxide concentration scenario. Approximately 89% of carbon released to the atmosphere by forest fire burning is in the form of carbon dioxide, 9% is carbon monoxide, and the remaining carbon is released as methane or non-methane hydrocarbons. It is estimated that forest fires in northern circumpolar countries contribute from 1-2% of the carbon released globally through biomass burning. Fire may be the agent by which a northerly shift of forest vegetation in Canada occurs. 13 refs., 2 figs

Carbon nanowalls synthesis by means of atmospheric dcPECVD method

International Nuclear Information System (INIS)

Mesko, Marcel; Kotrusz, Peter; Skakalova, Viera; Vretenar, Viliam; Hulman, Martin; Soltys, Jan

2012-01-01

Carbon nanowalls (CNWs) were grown by atmospheric dc plasma enhanced chemical vapour deposition method. Maintaining plasma at atmospheric pressure give us possibility to synthetize CNWs at high rate. By using two different liquid carbon sources we can control CNWs density. Growth of sparsely distributed CNWs can be achieved by using ethanol, while hexane gives densely packed CNWs films. (Copyright copyright 2012 WILEY-VCH Verlag GmbH and Co. KGaA, Weinheim)

The surface energy, water, carbon flux and their intercorrelated seasonality in a global climate-vegetation coupled model

International Nuclear Information System (INIS)

Li Dan.; Jinjun Ji

2007-01-01

The sensible and latent heat fluxes, representatives of the physical exchange processes of energy and water between land and air, are the two crucial variables controlling the surface energy partitioning related to temperature and humidity. The net primary production (NPP), the major carbon flux exchange between vegetation and atmosphere, is of great importance for the terrestrial ecosystem carbon cycle. The fluxes are simulated by a two-way coupled model, Atmosphere-Vegetation Interaction Model-Global Ocean-Atmosphere-Land System Model (AVIM-GOALS) in which the surface physical and physiological processes are coupled with general circulation model (GCM), and the global spatial and temporal variation of the fluxes is studied. The simulated terrestrial surface physical fluxes are consistent with the 40-yr European Centre for Medium-Range Weather Forecasts (ECMWF) Reanalysis (ERA40) in the global distribution, but the magnitudes are generally 20-40 W/m 2 underestimated. The annual NPP agrees well with the International Geosphere Biosphere Programme (IGBP) NPP data except for the lower value in northern high latitudes. The surface physical fluxes, leaf area index (LAI) and NPP of the global mid-latitudes, especially between 30 deg N-50 deg N, show great variation in annual oscillation amplitudes. And all physical and biological fields in northern mid-latitudes have the largest seasonality with a high statistical significance of 99.9%. The seasonality of surface physical fluxes, LAI and NPP are highly correlated with each other. The meridional three-peak pattern of seasonal change emerges in northern mid-latitudes, which indicates the interaction of topographical gradient variation of surface fluxes and vegetation phenology on these three latitudinal belts

The sensitivity of soil respiration to soil temperature, moisture, and carbon supply at the global scale.

Science.gov (United States)

Hursh, Andrew; Ballantyne, Ashley; Cooper, Leila; Maneta, Marco; Kimball, John; Watts, Jennifer

2017-05-01

Soil respiration (Rs) is a major pathway by which fixed carbon in the biosphere is returned to the atmosphere, yet there are limits to our ability to predict respiration rates using environmental drivers at the global scale. While temperature, moisture, carbon supply, and other site characteristics are known to regulate soil respiration rates at plot scales within certain biomes, quantitative frameworks for evaluating the relative importance of these factors across different biomes and at the global scale require tests of the relationships between field estimates and global climatic data. This study evaluates the factors driving Rs at the global scale by linking global datasets of soil moisture, soil temperature, primary productivity, and soil carbon estimates with observations of annual Rs from the Global Soil Respiration Database (SRDB). We find that calibrating models with parabolic soil moisture functions can improve predictive power over similar models with asymptotic functions of mean annual precipitation. Soil temperature is comparable with previously reported air temperature observations used in predicting Rs and is the dominant driver of Rs in global models; however, within certain biomes soil moisture and soil carbon emerge as dominant predictors of Rs. We identify regions where typical temperature-driven responses are further mediated by soil moisture, precipitation, and carbon supply and regions in which environmental controls on high Rs values are difficult to ascertain due to limited field data. Because soil moisture integrates temperature and precipitation dynamics, it can more directly constrain the heterotrophic component of Rs, but global-scale models tend to smooth its spatial heterogeneity by aggregating factors that increase moisture variability within and across biomes. We compare statistical and mechanistic models that provide independent estimates of global Rs ranging from 83 to 108 Pg yr -1 , but also highlight regions of uncertainty

Marine Atmospheric Corrosion of Carbon Steel: A Review.

Science.gov (United States)

Alcántara, Jenifer; Fuente, Daniel de la; Chico, Belén; Simancas, Joaquín; Díaz, Iván; Morcillo, Manuel

2017-04-13

The atmospheric corrosion of carbon steel is an extensive topic that has been studied over the years by many researchers. However, until relatively recently, surprisingly little attention has been paid to the action of marine chlorides. Corrosion in coastal regions is a particularly relevant issue due the latter's great importance to human society. About half of the world's population lives in coastal regions and the industrialisation of developing countries tends to concentrate production plants close to the sea. Until the start of the 21st century, research on the basic mechanisms of rust formation in Cl - -rich atmospheres was limited to just a small number of studies. However, in recent years, scientific understanding of marine atmospheric corrosion has advanced greatly, and in the authors' opinion a sufficient body of knowledge has been built up in published scientific papers to warrant an up-to-date review of the current state-of-the-art and to assess what issues still need to be addressed. That is the purpose of the present review. After a preliminary section devoted to basic concepts on atmospheric corrosion, the marine atmosphere, and experimentation on marine atmospheric corrosion, the paper addresses key aspects such as the most significant corrosion products, the characteristics of the rust layers formed, and the mechanisms of steel corrosion in marine atmospheres. Special attention is then paid to important matters such as coastal-industrial atmospheres and long-term behaviour of carbon steel exposed to marine atmospheres. The work ends with a section dedicated to issues pending, noting a series of questions in relation with which greater research efforts would seem to be necessary.

Marine Atmospheric Corrosion of Carbon Steel: A Review

Science.gov (United States)

Alcántara, Jenifer; de la Fuente, Daniel; Chico, Belén; Simancas, Joaquín; Díaz, Iván; Morcillo, Manuel

2017-01-01

The atmospheric corrosion of carbon steel is an extensive topic that has been studied over the years by many researchers. However, until relatively recently, surprisingly little attention has been paid to the action of marine chlorides. Corrosion in coastal regions is a particularly relevant issue due the latter’s great importance to human society. About half of the world’s population lives in coastal regions and the industrialisation of developing countries tends to concentrate production plants close to the sea. Until the start of the 21st century, research on the basic mechanisms of rust formation in Cl−-rich atmospheres was limited to just a small number of studies. However, in recent years, scientific understanding of marine atmospheric corrosion has advanced greatly, and in the authors’ opinion a sufficient body of knowledge has been built up in published scientific papers to warrant an up-to-date review of the current state-of-the-art and to assess what issues still need to be addressed. That is the purpose of the present review. After a preliminary section devoted to basic concepts on atmospheric corrosion, the marine atmosphere, and experimentation on marine atmospheric corrosion, the paper addresses key aspects such as the most significant corrosion products, the characteristics of the rust layers formed, and the mechanisms of steel corrosion in marine atmospheres. Special attention is then paid to important matters such as coastal-industrial atmospheres and long-term behaviour of carbon steel exposed to marine atmospheres. The work ends with a section dedicated to issues pending, noting a series of questions in relation with which greater research efforts would seem to be necessary. PMID:28772766

CO 2 Capture from Dilute Gases as a Component of Modern Global Carbon Management

KAUST Repository

Jones, Christopher W.

2011-01-01

The growing atmospheric CO2 concentration and its impact on climate have motivated widespread research and development aimed at slowing or stemming anthropogenic carbon emissions. Technologies for carbon capture and sequestration (CCS) employing mass separating agents that extract and purify CO2 from flue gas emanating from large point sources such as fossil fuel-fired electricity-generating power plants are under development. Recent advances in solvents, adsorbents, and membranes for postcombust- ion CO 2 capture are described here. Specifically, room-temperature ionic liquids, supported amine materials, mixed matrix and facilitated transport membranes, and metal-organic framework materials are highlighted. In addition, the concept of extracting CO2 directly from ambient air (air capture) as a means of reducing the global atmospheric CO2 concentration is reviewed. For both conventional CCS from large point sources and air capture, critical research needs are identified and discussed. © Copyright 2011 by Annual Reviews. All rights reserved.

CO 2 Capture from Dilute Gases as a Component of Modern Global Carbon Management

KAUST Repository

Jones, Christopher W.

2011-07-15

The growing atmospheric CO2 concentration and its impact on climate have motivated widespread research and development aimed at slowing or stemming anthropogenic carbon emissions. Technologies for carbon capture and sequestration (CCS) employing mass separating agents that extract and purify CO2 from flue gas emanating from large point sources such as fossil fuel-fired electricity-generating power plants are under development. Recent advances in solvents, adsorbents, and membranes for postcombust- ion CO 2 capture are described here. Specifically, room-temperature ionic liquids, supported amine materials, mixed matrix and facilitated transport membranes, and metal-organic framework materials are highlighted. In addition, the concept of extracting CO2 directly from ambient air (air capture) as a means of reducing the global atmospheric CO2 concentration is reviewed. For both conventional CCS from large point sources and air capture, critical research needs are identified and discussed. © Copyright 2011 by Annual Reviews. All rights reserved.

Fate of Chloromethanes in the Atmospheric Environment: Implications for Human Health, Ozone Formation and Depletion, and Global Warming Impacts

Science.gov (United States)

Tsai, Wen-Tien

2017-01-01

Among the halogenated hydrocarbons, chloromethanes (i.e., methyl chloride, CH3Cl; methylene chloride, CH2Cl2; chloroform, CHCl3; and carbon tetrachloride, CCl4) play a vital role due to their extensive uses as solvents and chemical intermediates. This article aims to review their main chemical/physical properties and commercial/industrial uses, as well as the environment and health hazards posed by them and their toxic decomposition products. The environmental properties (including atmospheric lifetime, radiative efficiency, ozone depletion potential, global warming potential, photochemical ozone creation potential, and surface mixing ratio) of these chlorinated methanes are also reviewed. In addition, this paper further discusses their atmospheric fates and human health implications because they are apt to reside in the lower atmosphere when released into the environment. According to the atmospheric degradation mechanism, their toxic degradation products in the troposphere include hydrogen chloride (HCl), carbon monoxide (CO), chlorine (Cl2), formyl chloride (HCOCl), carbonyl chloride (COCl2), and hydrogen peroxide (H2O2). Among them, COCl2 (also called phosgene) is a powerful irritating gas, which is easily hydrolyzed or thermally decomposed to form hydrogen chloride. PMID:29051455

Response of a tundra ecosystem to elevated atmospheric carbon dioxide and CO{sub 2}-induced climate change. Annual technical report

Energy Technology Data Exchange (ETDEWEB)

Oechel, W.C.

1993-02-01

Northern ecosystems contain up to 455 Gt of C in the soil active layer and upper permafrost, which is equivalent to approximately 60% of the carbon currently in the atmosphere as CO{sub 2}. Much of this carbon is stored in the soil as dead organic matter. Its fate is subject to the net effects of global change on the plant and soil systems of northern ecosystems. The arctic alone contains about 60 Gt C, 90% of which is present in the soil active layer and upper permafrost, and is assumed to have been a sink for CO{sub 2} during the historic and recent geologic past. Depending on the nature, rate, and magnitude of global environmental change, the arctic may have a positive or negative feedback on global change. Results from the DOE- funded research efforts of 1990 and 1991 indicate that the arctic has become a source of CO{sub 2} to the atmosphere. Measurements made in the Barrow, Alaska region during 1992 support these results. This change coincides with recent climatic variation in the arctic, and suggests a positive feedback of arctic ecosystems on atmospheric CO{sub 2} and global change. There are obvious potential errors in scaling plot level measurements to landscape, mesoscale, and global spatial scales. In light of the results from the recent DOE-funded research, and the remaining uncertainties regarding the change in arctic ecosystem function due to high latitude warming, a revised set of research goals is proposed for the 1993--94 year. The research proposed in this application has four principal aspects: (A) Long- term response of arctic plants and ecosystems to elevated atmospheric CO{sub 2}. (B) Circumpolar patterns of net ecosystem CO{sub 2} flux. (C) In situ controls by temperature and moisture on net ecosystem CO{sub 2} flux. (D) Scaling of CO{sub 2} flux from plot, to landscape, to regional scales.

INTRODUCTION: Anticipated changes in the global atmospheric water cycle

Science.gov (United States)

Allan, Richard P.; Liepert, Beate G.

2010-06-01

The atmospheric branch of the water cycle, although containing just a tiny fraction of the Earth's total water reserves, presents a crucial interface between the physical climate (such as large-scale rainfall patterns) and the ecosystems upon which human societies ultimately depend. Because of the central importance of water in the Earth system, the question of how the water cycle is changing, and how it may alter in future as a result of anthropogenic changes, present one of the greatest challenges of this century. The recent Intergovernmental Panel on Climate Change report on Climate Change and Water (Bates et al 2008) highlighted the increasingly strong evidence of change in the global water cycle and associated environmental consequences. It is of critical importance to climate prediction and adaptation strategies that key processes in the atmospheric water cycle are precisely understood and determined, from evaporation at the surface of the ocean, transport by the atmosphere, condensation as cloud and eventual precipitation, and run-off through rivers following interaction with the land surface, sub-surface, ice, snow and vegetation. The purpose of this special focus issue of Environmental Research Letters on anticipated changes in the global atmospheric water cycle is to consolidate the recent substantial advances in understanding past, present and future changes in the global water cycle through evidence built upon theoretical understanding, backed up by observations and borne out by climate model simulations. Thermodynamic rises in water vapour provide a central constraint, as discussed in a guest editorial by Bengtsson (2010). Theoretical implications of the Clausius-Clapeyron equation are presented by O'Gorman and Muller (2010) and with reference to a simple model (Sherwood 2010) while observed humidity changes confirm these anticipated responses at the land and ocean surface (Willett et al 2008). Rises in low-level moisture are thought to fuel an

The atmosphere as a global commons : responsible caring and equitable sharing

Energy Technology Data Exchange (ETDEWEB)

Hallman, D.G. [World Council of Churches, Toronto, ON (Canada)

2000-06-01

The World Council of Churches (WCC) views climate change issues from a theological and ethical perspective. This justice statement regarding climate change was prepared by the WCC in anticipation of the sixth session of the Conference of Parties (COP6) held in the Hague, Netherlands in November 2000. The statement presents the atmosphere as a global commons which envelops the Earth, nurturing and protecting life. Their statement urges that economic and political powers cannot be allowed to hinder the health of the atmosphere nor claim possession of it. The WCC pairs human responsibility with climate change and recognizes that the problem is caused largely by rich industrialized countries, the consequences of which will be suffered mostly by developing nations and by future generations. The statement emphasized that we must be held responsible for the destructive impact of our actions which are leading to climate change. The WCC argued that emissions trading under the Kyoto Protocol would violate the criterion of ecological effectiveness because it would not ensure a reduction in actual emissions. Trading mechanisms such as proposed under the Clean Development Mechanism would raise issues of equity and justice and would risk exacerbating inequities between rich and poor countries. The WCC made several recommendations for COP6. One of them was to refocus climate change negotiations on to options that meet the criteria of environmental effectiveness, equity, responsibility and economic efficiency with priority given to emissions reduction strategies in high per capita polluting countries. This statement also made reference to the use of a Global Atmospheric Commons Fund which would help impoverished countries to move towards a non-carbon economy focusing on renewable energy sources such as solar, biomass, wind and small scale hydroelectric.

Carbon Dioxide Information Analysis Center and World Data Center for Atmospheric Trace Gases Fiscal Year 1999 Annual Report

Energy Technology Data Exchange (ETDEWEB)

Cushman, R.M.

2000-03-31

The Carbon Dioxide Information Analysis Center (CDIAC), which includes the World Data Center (WDC) for Atmospheric Trace Gases, is the primary global-change data and information analysis center of the Department of Energy (DOE). More than just an archive of data sets and publications, CDIAC has--since its inception in 1982--enhanced the value of its holdings through intensive quality assurance, documentation, and integration. Whereas many traditional data centers are discipline-based (for example, meteorology or oceanography), CDIAC's scope includes potentially anything and everything that would be of value to users concerned with the greenhouse effect and global climate change, including concentrations of carbon dioxide (CO{sub 2}) and other radiatively active gases in the atmosphere; the role of the terrestrial biosphere and the oceans in the biogeochemical cycles of greenhouse gases; emissions of CO{sub 2} and other trace gases to the atmosphere; long-term climate trends; the effects of elevated CO{sub 2} on vegetation; and the vulnerability of coastal areas to rising sea level. CDIAC is located within the Environmental Sciences Division (ESD) at Oak Ridge National Laboratory (ORNL) in Oak Ridge, Tennessee. CDIAC is co-located with ESD researchers investigating global-change topics, such as the global carbon cycle and the effects of carbon dioxide on vegetation. CDIAC staff are also connected with current ORNL research on related topics, such as renewable energy and supercomputing technologies. CDIAC is supported by the Environmental Sciences Division (Jerry Elwood, Acting Director) of DOE's Office of Biological and Environmental Research. CDIAC's FY 1999 budget was 2.2M dollars. CDIAC represents the DOE in the multi-agency Global Change Data and Information System. Bobbi Parra, and Wanda Ferrell on an interim basis, is DOE's Program Manager with responsibility for CDIAC. CDIAC comprises three groups, Global Change Data, Computer Systems, and

Audit of the global carbon budget: estimate errors and their impact on uptake uncertainty

Science.gov (United States)

Ballantyne, A. P.; Andres, R.; Houghton, R.; Stocker, B. D.; Wanninkhof, R.; Anderegg, W.; Cooper, L. A.; DeGrandpre, M.; Tans, P. P.; Miller, J. B.; Alden, C.; White, J. W. C.

2015-04-01

Over the last 5 decades monitoring systems have been developed to detect changes in the accumulation of carbon (C) in the atmosphere and ocean; however, our ability to detect changes in the behavior of the global C cycle is still hindered by measurement and estimate errors. Here we present a rigorous and flexible framework for assessing the temporal and spatial components of estimate errors and their impact on uncertainty in net C uptake by the biosphere. We present a novel approach for incorporating temporally correlated random error into the error structure of emission estimates. Based on this approach, we conclude that the 2σ uncertainties of the atmospheric growth rate have decreased from 1.2 Pg C yr-1 in the 1960s to 0.3 Pg C yr-1 in the 2000s due to an expansion of the atmospheric observation network. The 2σ uncertainties in fossil fuel emissions have increased from 0.3 Pg C yr-1 in the 1960s to almost 1.0 Pg C yr-1 during the 2000s due to differences in national reporting errors and differences in energy inventories. Lastly, while land use emissions have remained fairly constant, their errors still remain high and thus their global C uptake uncertainty is not trivial. Currently, the absolute errors in fossil fuel emissions rival the total emissions from land use, highlighting the extent to which fossil fuels dominate the global C budget. Because errors in the atmospheric growth rate have decreased faster than errors in total emissions have increased, a ~20% reduction in the overall uncertainty of net C global uptake has occurred. Given all the major sources of error in the global C budget that we could identify, we are 93% confident that terrestrial C uptake has increased and 97% confident that ocean C uptake has increased over the last 5 decades. Thus, it is clear that arguably one of the most vital ecosystem services currently provided by the biosphere is the continued removal of approximately half of atmospheric CO2 emissions from the atmosphere

Amazon River carbon dioxide outgassing fuelled by wetlands

NARCIS (Netherlands)

Abril, G.; Martinez, J.M.; Artigas, L.F.; Moreira-Turcq, P.; Benedetti, M.F.; Vidal, L.; Meziane, T.; Kim, J.-H.; Bernardes, M.C.; Savoye, N.; Deborde, J.; Souza, E.L.; Alberic, P.; de Souza, M.F.L.; Roland, F.

2014-01-01

River systems connect the terrestrial biosphere, the atmosphere and the ocean in the global carbon cycle(1). A recent estimate suggests that up to 3 petagrams of carbon per year could be emitted as carbon dioxide (CO2) from global inland waters, offsetting the carbon uptake by terrestrial

Origin of particulate organic carbon in the marine atmosphere as indicated by it stable carbon isotopic composition

International Nuclear Information System (INIS)

Chesselet, R.; Fontugne, M.; Buat-Menard, P.; Ezat, U.; Lambert, C.E.

1981-01-01

Organic carbon concentration and isotopic composition were determined in samples of atmospheric particulate matter collected in 1979 at remote marine locations (Enewetak atoll, Sargasso Sea) during the SEAREX (Sea-Air Exchange) program field experiments. Atmospheric Particulate Organic Carbon (POC) concentrations were found to be in the range of 0.3 to 1.2 mg. m -3 , in agreement with previous literature data. The major mass of POC was found on the smallest particles (r 13 C/ 12 C of the small particles is close to the one expected (d 13 C = 26 +- 2 0 //sub infinity/) for atmospheric POC of continental origin. For all the samples analysed so far, it appears that more than 80% of atmospheric POC over remote marine areas is of continental origin. This can be explained either by long-range transport of small sized continental organic aserosols or by the production of POC in the marine atmosphere from a vapor phase organic carbon pool of continental origin. The POC in the large size fraction of marine aerosols ( 13 C = -21 +- 2 0 / 00 ) for POC associated with sea-salt droplets transported to the marine atmosphere

Evolution and challenges of dynamic global vegetation models for some aspects of plant physiology and elevated atmospheric CO2.

Science.gov (United States)

Rezende, L F C; Arenque, B C; Aidar, S T; Moura, M S B; Von Randow, C; Tourigny, E; Menezes, R S C; Ometto, J P H B

2016-07-01

Dynamic global vegetation models (DGVMs) simulate surface processes such as the transfer of energy, water, CO2, and momentum between the terrestrial surface and the atmosphere, biogeochemical cycles, carbon assimilation by vegetation, phenology, and land use change in scenarios of varying atmospheric CO2 concentrations. DGVMs increase the complexity and the Earth system representation when they are coupled with atmospheric global circulation models (AGCMs) or climate models. However, plant physiological processes are still a major source of uncertainty in DGVMs. The maximum velocity of carboxylation (Vcmax), for example, has a direct impact over productivity in the models. This parameter is often underestimated or imprecisely defined for the various plant functional types (PFTs) and ecosystems. Vcmax is directly related to photosynthesis acclimation (loss of response to elevated CO2), a widely known phenomenon that usually occurs when plants are subjected to elevated atmospheric CO2 and might affect productivity estimation in DGVMs. Despite this, current models have improved substantially, compared to earlier models which had a rudimentary and very simple representation of vegetation-atmosphere interactions. In this paper, we describe this evolution through generations of models and the main events that contributed to their improvements until the current state-of-the-art class of models. Also, we describe some main challenges for further improvements to DGVMs.

Global ocean carbon uptake: magnitude, variability and trends

Directory of Open Access Journals (Sweden)

R. Wanninkhof

2013-03-01

Full Text Available The globally integrated sea–air anthropogenic carbon dioxide (CO2 flux from 1990 to 2009 is determined from models and data-based approaches as part of the Regional Carbon Cycle Assessment and Processes (RECCAP project. Numerical methods include ocean inverse models, atmospheric inverse models, and ocean general circulation models with parameterized biogeochemistry (OBGCMs. The median value of different approaches shows good agreement in average uptake. The best estimate of anthropogenic CO2 uptake for the time period based on a compilation of approaches is −2.0 Pg C yr−1. The interannual variability in the sea–air flux is largely driven by large-scale climate re-organizations and is estimated at 0.2 Pg C yr−1 for the two decades with some systematic differences between approaches. The largest differences between approaches are seen in the decadal trends. The trends range from −0.13 (Pg C yr−1 decade−1 to −0.50 (Pg C yr−1 decade−1 for the two decades under investigation. The OBGCMs and the data-based sea–air CO2 flux estimates show appreciably smaller decadal trends than estimates based on changes in carbon inventory suggesting that methods capable of resolving shorter timescales are showing a slowing of the rate of ocean CO2 uptake. RECCAP model outputs for five decades show similar differences in trends between approaches.

Historical and future perspectives of global soil carbon response to climate and land-use changes

Science.gov (United States)

Eglin, T.; Ciais, P.; Piao, S. L.; Barre, P.; Bellassen, V.; Cadule, P.; Chenu, C.; Gasser, T.; Koven, C.; Reichstein, M.; Smith, P.

2010-11-01

ABSTRACT In this paper, we attempt to analyse the respective influences of land-use and climate changes on the global and regional balances of soil organic carbon (SOC) stocks. Two time periods are analysed: the historical period 1901-2000 and the period 2000-2100. The historical period is analysed using a synthesis of published data as well as new global and regional model simulations, and the future is analysed using models only. Historical land cover changes have resulted globally in SOC release into the atmosphere. This human induced SOC decrease was nearly balanced by the net SOC increase due to higher CO2 and rainfall. Mechanization of agriculture after the 1950s has accelerated SOC losses in croplands, whereas development of carbon-sequestering practices over the past decades may have limited SOC loss from arable soils. In some regions (Europe, China and USA), croplands are currently estimated to be either a small C sink or a small source, but not a large source of CO2 to the atmosphere. In the future, according to terrestrial biosphere and climate models projections, both climate and land cover changes might cause a net SOC loss, particularly in tropical regions. The timing, magnitude, and regional distribution of future SOC changes are all highly uncertain. Reducing this uncertainty requires improving future anthropogenic CO2 emissions and land-use scenarios and better understanding of biogeochemical processes that control SOC turnover, for both managed and un-managed ecosystems.

Carbon sequestration.

Science.gov (United States)

Lal, Rattan

2008-02-27

Developing technologies to reduce the rate of increase of atmospheric concentration of carbon dioxide (CO2) from annual emissions of 8.6PgCyr-1 from energy, process industry, land-use conversion and soil cultivation is an important issue of the twenty-first century. Of the three options of reducing the global energy use, developing low or no-carbon fuel and sequestering emissions, this manuscript describes processes for carbon (CO2) sequestration and discusses abiotic and biotic technologies. Carbon sequestration implies transfer of atmospheric CO2 into other long-lived global pools including oceanic, pedologic, biotic and geological strata to reduce the net rate of increase in atmospheric CO2. Engineering techniques of CO2 injection in deep ocean, geological strata, old coal mines and oil wells, and saline aquifers along with mineral carbonation of CO2 constitute abiotic techniques. These techniques have a large potential of thousands of Pg, are expensive, have leakage risks and may be available for routine use by 2025 and beyond. In comparison, biotic techniques are natural and cost-effective processes, have numerous ancillary benefits, are immediately applicable but have finite sink capacity. Biotic and abiotic C sequestration options have specific nitches, are complementary, and have potential to mitigate the climate change risks.

An Analytical Framework for the Steady State Impact of Carbonate Compensation on Atmospheric CO2

Science.gov (United States)

Omta, Anne Willem; Ferrari, Raffaele; McGee, David

2018-04-01

The deep-ocean carbonate ion concentration impacts the fraction of the marine calcium carbonate production that is buried in sediments. This gives rise to the carbonate compensation feedback, which is thought to restore the deep-ocean carbonate ion concentration on multimillennial timescales. We formulate an analytical framework to investigate the impact of carbonate compensation under various changes in the carbon cycle relevant for anthropogenic change and glacial cycles. Using this framework, we show that carbonate compensation amplifies by 15-20% changes in atmospheric CO2 resulting from a redistribution of carbon between the atmosphere and ocean (e.g., due to changes in temperature, salinity, or nutrient utilization). A counterintuitive result emerges when the impact of organic matter burial in the ocean is examined. The organic matter burial first leads to a slight decrease in atmospheric CO2 and an increase in the deep-ocean carbonate ion concentration. Subsequently, enhanced calcium carbonate burial leads to outgassing of carbon from the ocean to the atmosphere, which is quantified by our framework. Results from simulations with a multibox model including the minor acids and bases important for the ocean-atmosphere exchange of carbon are consistent with our analytical predictions. We discuss the potential role of carbonate compensation in glacial-interglacial cycles as an example of how our theoretical framework may be applied.

Crust-mantle branch of the global carbon cycle and origin of deep-seated hydrocarbons

Directory of Open Access Journals (Sweden)

Sorokhtin N. O.

2018-03-01

Full Text Available The processes of multi-stage and polycyclic transformation and transfer of carbon in the crust and mantle have been described. The sediments drawn in the plate underthrust zones break down, become transformed and altered by metamorphic events, and part of the newly formed carbon compounds is transferred by the mantle convective currents to rift zones of the mid-oceanic ridges and carried up to the surface as hydrocarbons of various composition and carbon dioxide. This material becomes re-deposited on the sea floor as sediments forming carbonaceous and carbon-bearing units. As a result of multi-stage mechanism of physical and chemical transformations in the crust-mantle areas of the Earth hydrocarbon compounds acquire features of abiogenic origin remaining, in fact, exogenic. The revealed crust-mantle carbon cycle represents part of a global process for the cyclic carbon transfer from the atmosphere to the mantle and back. The scale of its manifestation is likely not so wide, and numerous small (mm and portions of millimeters particles of exogenic substance and dispersed carbon drawn in the plate underthrust zones form a stable geochemical tail of the crustal direction in the mantle propagating in the plane of convective currents motion. The scale of this process may be indirectly suggested by the volumes of hydrocarbon and carbon dioxide de-gassing and hydrogen in the rift systems of the Earth crust. The amount of generated hydrocarbon gases with deep-seated origin cannot form large gas and oil-and-gas fields since their significant part is transferred to the atmosphere. Just some portion of compounds may be deposited in oceanic sediments and generate gas-hydrate pools.

Water vs. carbon: An evaluation of SMAP soil moisture and OCO-2 solar-induced fluorescence to characterize global plant stress

Science.gov (United States)

Purdy, A. J.; Fisher, J.; Goulden, M.; Randerson, J. T.; Famiglietti, J. S.

2017-12-01

Plants link the carbon and water cycles through photosynthesis and evapotranspiration (ET). When plants take in CO2 for photosynthesis, water evaporates to the atmosphere. This exchange of carbon and water is sensitive to a number of environmental variables including: soil water availability, temperature, atmospheric water vapor, and radiation. When the atmospheric demand for water is high, plants avoid hydraulic failure by regulating the amount of water exiting leaves at the expense of inhibiting carbon uptake. Over time, stress caused by this response limits plant growth and can even result in death by carbon starvation. With increasing atmospheric demand for water, impending expansion of arid regions, and more frequent droughts, understanding how vegetation responds to regulate photosynthesis and ET is important to quantify potential feedbacks between the carbon and water cycles. Despite its importance, to what extent plants respond to stressful conditions is an open science question. An important step forward is to characterize the dominant controls in these stress events and identify geographic areas that are vulnerable to climate change. The 2015-2016 El Nino and subsequent 2016-2017 La Nina transition provides an opportunity to quantify the extent and magnitude of vegetation regulation of these carbon and water variables in response to changes in environmental conditions. We present results from a space-based analysis using global observations of solar induced fluorescence (SIF) from the Orbiting Carbon Observatory-2 (OCO-2), soil moisture from Soil Moisture Active Passive (SMAP), and two widely used ET models (PT-JPL and MOD-16) to characterize the dominant controls on gross primary production and ET.

Climate Impacts of CALIPSO-Guided Corrections to Black Carbon Aerosol Vertical Distributions in a Global Climate Model

International Nuclear Information System (INIS)

Kovilakam, Mahesh; Mahajan, Salil; Saravanan, R.; Chang, Ping

2017-01-01

Here, we alleviate the bias in the tropospheric vertical distribution of black carbon aerosols (BC) in the Community Atmosphere Model (CAM4) using the Cloud-Aerosol and Infrared Pathfinder Satellite Observations (CALIPSO)-derived vertical profiles. A suite of sensitivity experiments are conducted with 1x, 5x, and 10x the present-day model estimated BC concentration climatology, with (corrected, CC) and without (uncorrected, UC) CALIPSO-corrected BC vertical distribution. The globally averaged top of the atmosphere radiative flux perturbation of CC experiments is ~8–50% smaller compared to uncorrected (UC) BC experiments largely due to an increase in low-level clouds. The global average surface temperature increases, the global average precipitation decreases, and the ITCZ moves northward with the increase in BC radiative forcing, irrespective of the vertical distribution of BC. Further, tropical expansion metrics for the poleward extent of the Northern Hemisphere Hadley cell (HC) indicate that simulated HC expansion is not sensitive to existing model biases in BC vertical distribution.

Atmospheric carbon dioxide removal: long-term consequences and commitment

International Nuclear Information System (INIS)

Cao Long; Caldeira, Ken

2010-01-01

Carbon capture from ambient air has been proposed as a mitigation strategy to counteract anthropogenic climate change. We use an Earth system model to investigate the response of the coupled climate-carbon system to an instantaneous removal of all anthropogenic CO 2 from the atmosphere. In our extreme and idealized simulations, anthropogenic CO 2 emissions are halted and all anthropogenic CO 2 is removed from the atmosphere at year 2050 under the IPCC A2 CO 2 emission scenario when the model-simulated atmospheric CO 2 reaches 511 ppm and surface temperature reaches 1.8 deg. C above the pre-industrial level. In our simulations a one-time removal of all anthropogenic CO 2 in the atmosphere reduces surface air temperature by 0.8 deg. C within a few years, but 1 deg. C surface warming above pre-industrial levels lasts for several centuries. In other words, a one-time removal of 100% excess CO 2 from the atmosphere offsets less than 50% of the warming experienced at the time of removal. To maintain atmospheric CO 2 and temperature at low levels, not only does anthropogenic CO 2 in the atmosphere need to be removed, but anthropogenic CO 2 stored in the ocean and land needs to be removed as well when it outgasses to the atmosphere. In our simulation to maintain atmospheric CO 2 concentrations at pre-industrial levels for centuries, an additional amount of CO 2 equal to the original CO 2 captured would need to be removed over the subsequent 80 years.

Carbon cycle

Energy Technology Data Exchange (ETDEWEB)

Jaeger, J; Halbritter, G; Neumann-Hauf, G

1982-05-01

This report contains a review of literature on the subjects of the carbon cycle, the increase of the atmospheric CO/sub 2/ concentration and the possible impacts of an increased CO/sub 2/ concentration on the climate. In addition to this survey, the report discusses the questions that are still open and the resulting research needs. During the last twenty years a continual increase of the atmospheric carbon dioxide concentration by about 1-2 ppm per years has been observed. In 1958 the concentration was 315 ppm and this increased to 336 ppm in 1978. A rough estimate shows that the increase of the atmospheric carbon dioxide concentration is about half of the amount of carbon dioxide added to the atmosphere by the combustion of fossil fuels. Two possible sinks for the CO/sub 2/ released into the atmosphere are known: the ocean and the biota. The role of the biota is, however, unclear, since it can act both as a sink and as a source. Most models of the carbon cycle are one-dimensional and cannot be used for accurate predictions. Calculations with climate models have shown that an increased atmospheric CO/sub 2/ concentration leads to a warming of the earth's surface and lower atmosphere. Calculations show that a doubling of the atmospheric CO/sub 2/-concentration would lead to a net heating of the lower atmosphere and earth's surface by a global average of about 4 W m/sup -2/. Greater uncertainties arise in estimating the change in surface temperature resulting from this change in heating rate. It is estimated that the global average annual surface temperature would change between 1.5 and 4.5 K. There are, however, latitudinal and seasonal variations of the impact of increased CO/sub 2/ concentration. Other meteorological variables (e.g. precipitation, wind speed etc.) would also be changed. It appears that the impacts of the other products of fossil fuel combustion are unlikely to counteract the impacts of CO/sub 2/ on the climate.

Forest carbon sink: A potential forest investment

Science.gov (United States)

Zheng, Chaocheng; Zhang, Yi; Cheng, Dongxiang

2017-01-01

A major problem being confronted to our human society currently is that the global temperature is undoubtedly considered to be rising significantly year by year due to abundant human factors releasing carbon dioxide to around atmosphere. The problem of increasing atmospheric carbon dioxide can be addressed in a number of ways. One of these is forestry and forest management. Hence, this paper investigates a number of current issues related to mitigating the global warming problem from the point of forestry view previous to discussion on ongoing real-world activities utilizing forestry specifically to sequester carbon.

Carbon dioxide and the greenhouse effect: an unresolved problem

Energy Technology Data Exchange (ETDEWEB)

Smith, I M

1978-01-01

This paper evaluates current scientific literature concerned with the accumulation of carbon dioxide in the atmosphere. The extent and possible causes of natural variations in global climate are outlined as a background to potential variations due to human activity. Estimates are given on relative contributions of carbon dioxide to the atmosphere due to fossil fuel combustion, deforestation and other land modifications. The possibility of a rise in global temperature as a result of increasing the amount of carbon dioxide in the atmosphere is discussed including model predictions, natural factors which could compensate for or emphasize a warming effect, and the implications if extensive warming actually occurred. Carbon dioxide disposal is discussed but there appears to be no practicable long-term means of accomplishing this. It is concluded that there is no evidence of a rise in global temperature due to carbon dioxide at present. Predictions, which involve a high degree of uncertainty, indicate that the global temperature could rise appreciably in the next century. An increase in precipitation rate is also expected.

Globalizing carbon lock-in

International Nuclear Information System (INIS)

Unruh, Gregory C.; Carrillo-Hermosilla, Javier

2006-01-01

This paper extends the arguments surrounding carbon lock-in elaborated in Unruh (Energy Policy 28 (2000) 817; 30 (2002) 317) to countries currently undergoing industrialization. It argues that, for numerous reasons, industrializing countries are unlikely to leapfrog carbon intensive energy development. On the contrary, carbon lock-in may be globalizing and could further constrain climate change mitigation options. It is then argued that many policy recommendations ignore carbon lock-in, possibly limiting their potential for successful implementation. The paper then discusses four policy approaches that appear to have advantages given lock-in conditions. It is recognized, however, that relative ease of implementation does not necessarily equate with superiority. Instead, it is merely a path dependent outcome of past development decisions. Pursuing policies on the basis of relative implementation ease may help address the issue of climate change, but could also result in sub-optimal outcomes along other dimensions of sustainable development

Production of activated carbon by using pyrolysis process in an ammonia atmosphere

Science.gov (United States)

Indayaningsih, N.; Destyorini, F.; Purawiardi, R. I.; Insiyanda, D. R.; Widodo, H.

2017-04-01

Activated carbon is materials that have wide applications, including supercapacitor materials, absorbent in chemical industry, and absorbent material in the chemical industry. This study has carried out for the manufacturing of activated carbon from inexpensive materials through efficient processes. Carbon material was made from coconut fibers through pyrolysis process at temperature of 650, 700, 750 and 800°C. Aim of this study was to obtain carbon material that has a large surface area. Pyrolysis process is carried out in an inert atmosphere (N2 gas) at a temperature of 450°C for 30 minutes, followed by pyrolysis process in an ammonia atmosphere at 800°C for 2 hours. The pyrolysis results showed that the etching process in ammonia is occurred; as it obtained some greater surface area when compared with the pyrolisis process in an atmosphere by inert gas only. The resulted activated carbon also showed to have good properties in surface area and total pore volume.

A New Global LAI Product and Its Use for Terrestrial Carbon Cycle Estimation

Science.gov (United States)

Chen, J. M.; Liu, R.; Ju, W.; Liu, Y.

2014-12-01

For improving the estimation of the spatio-temporal dynamics of the terrestrial carbon cycle, a new time series of the leaf area index (LAI) is generated for the global land surface at 8 km resolution from 1981 to 2012 by combining AVHRR and MODIS satellite data. This product differs from existing LAI products in the following two aspects: (1) the non-random spatial distribution of leaves with the canopy is considered, and (2) the seasonal variation of the vegetation background is included. The non-randomness of the leaf spatial distribution in the canopy is considered using the second vegetation structural parameter named clumping index (CI), which quantifies the deviation of the leaf spatial distribution from the random case. Using the MODIS Bidirectional Reflectance Distribution Function product, a global map of CI is produced at 500 m resolution. In our LAI algorithm, CI is used to convert the effective LAI obtained from mono-angle remote sensing into the true LAI, otherwise LAI would be considerably underestimated. The vegetation background is soil in crop, grass and shrub but includes soil, grass, moss, and litter in forests. Through processing a large volume of MISR data from 2000 to 2010, monthly red and near-infrared reflectances of the vegetation background is mapped globally at 1 km resolution. This new LAI product has been validated extensively using ground-based LAI measurements distributed globally. In carbon cycle modeling, the use of CI in addition to LAI allows for accurate separation of sunlit and shaded leaves as an important step in terrestrial photosynthesis and respiration modeling. Carbon flux measurements over 100 sites over the globe are used to validate an ecosystem model named Boreal Ecosystem Productivity Simulator (BEPS). The validated model is run globally at 8 km resolution for the period from 1981 to 2012 using the LAI product and other spatial datasets. The modeled results suggest that changes in vegetation structure as quantified

Information management for global environmental change, including the Carbon Dioxide Information Analysis Center

Energy Technology Data Exchange (ETDEWEB)

Stoss, F.W. [Oak Ridge National Lab., TN (United States). Carbon Dioxide Information Analysis Center

1994-06-01

The issue of global change is international in scope. A body of international organizations oversees the worldwide coordination of research and policy initiatives. In the US the National Science and Technology Council (NSTC) was established in November of 1993 to provide coordination of science, space, and technology policies throughout the federal government. NSTC is organized into nine proposed committees. The Committee on Environmental and Natural Resources (CERN) oversees the US Department of Energy`s Global Change Research Program (USGCRP). As part of the USGCRP, the US Department of Energy`s Global Change Research Program aims to improve the understanding of Earth systems and to strengthen the scientific basis for the evaluation of policy and government action in response to potential global environmental changes. This paper examines the information and data management roles of several international and national programs, including Oak Ridge National Laboratory`s (ORNL`s) global change information programs. An emphasis will be placed on the Carbon Dioxide Information Analysis Center (CDIAC), which also serves as the World Data Center-A for Atmospheric Trace Gases.

Evaluating the effects of terrestrial ecosystems, climate and carbon dioxide on weathering over geological time: a global-scale process-based approach

Science.gov (United States)

Taylor, Lyla L.; Banwart, Steve A.; Valdes, Paul J.; Leake, Jonathan R.; Beerling, David J.

2012-01-01

Global weathering of calcium and magnesium silicate rocks provides the long-term sink for atmospheric carbon dioxide (CO2) on a timescale of millions of years by causing precipitation of calcium carbonates on the seafloor. Catchment-scale field studies consistently indicate that vegetation increases silicate rock weathering, but incorporating the effects of trees and fungal symbionts into geochemical carbon cycle models has relied upon simple empirical scaling functions. Here, we describe the development and application of a process-based approach to deriving quantitative estimates of weathering by plant roots, associated symbiotic mycorrhizal fungi and climate. Our approach accounts for the influence of terrestrial primary productivity via nutrient uptake on soil chemistry and mineral weathering, driven by simulations using a dynamic global vegetation model coupled to an ocean–atmosphere general circulation model of the Earth's climate. The strategy is successfully validated against observations of weathering in watersheds around the world, indicating that it may have some utility when extrapolated into the past. When applied to a suite of six global simulations from 215 to 50 Ma, we find significantly larger effects over the past 220 Myr relative to the present day. Vegetation and mycorrhizal fungi enhanced climate-driven weathering by a factor of up to 2. Overall, we demonstrate a more realistic process-based treatment of plant fungal–geosphere interactions at the global scale, which constitutes a first step towards developing ‘next-generation’ geochemical models. PMID:22232768

Seasonal and global behavior of water vapor in the Mars atmosphere: Complete global results of the Viking atmospheric water detector experiment

International Nuclear Information System (INIS)

Jakosky, B.M.; Farmer, C.B.

1982-01-01

The water vapor content of the Mars atmosphere was measured from the Viking Orbiter Mars Atmospheric Water Detectors (MAWD) for a period of more than 1 Martian year, from June 1976 through April 1979. Results are presented in the form of global maps of column abundance for 24 periods throughout each Mars year. The data reduction incorporates spatial and seasonal variations in surface pressure and supplements earlier published versions of less complete data

Human impacts on 20th century fire dynamics and implications for global carbon and water trajectories

Science.gov (United States)

Li, Fang; Lawrence, David M.; Bond-Lamberty, Ben

2018-03-01

Fire is a fundamental Earth system process and the primary ecosystem disturbance on the global scale. It affects carbon and water cycles through changing terrestrial ecosystems, and at the same time, is regulated by weather and climate, vegetation characteristics, and, importantly, human ignitions and suppression (i.e., the direct human effect on fire). Here, we utilize the Community Land Model version 4.5 (CLM4.5) to quantify the impacts of changes in human ignition and suppression on fire dynamics and associated carbon and water cycles. We find that the impact is to significantly reduce the 20th century global burned area by a century average of 38 Mha/yr and by 103 Mha/yr at the end of the century. Land carbon gain is weakened by 17% over the 20th century, mainly due to increased human deforestation fires and associated escape fires (i.e., degradation fires) in the tropical humid forests, even though the decrease in burned area in many other regions due to human fire suppression acts to increase land carbon gain. The direct human effect on fire weakens the upward trend in global runoff throughout the century by 6% and enhances the upward trend in global evapotranspiration since 1945 by 7%. In addition, the above impacts in densely populated, highly developed (if population density > 0.1 person/km2), or moderately populated and developed regions are of opposite sign to those in other regions. Our study suggests that particular attention should be paid to human deforestation and degradation fires in the tropical humid forests when reconstructing and projecting fire carbon emissions and net atmosphere-land carbon exchange and estimating resultant impacts of direct human effect on fire.

Human impacts on 20th century fire dynamics and implications for global carbon and water trajectories

Energy Technology Data Exchange (ETDEWEB)

Li, Fang; Lawrence, David M.; Bond-Lamberty, Ben

2018-03-01

Fire is a fundamental Earth system process and the primary ecosystem disturbance on the global scale. It affects carbon and water cycles through changing terrestrial ecosystems, and at the same time, is regulated by weather and climate, vegetation characteristics, and, importantly, human ignitions and suppression (i.e., the direct human effect on fire). Here, we utilize the Community Land Model version 4.5 (CLM4.5) to quantify the impacts of changes in human ignition and suppression on fire dynamics and associated carbon and water cycles. We find that the impact is to significantly reduce the 20th century global burned area by a century average of 38 Mha/yr and by 103 Mha/yr at the end of the century. Land carbon gain is weakened by 17% over the 20th century, mainly due to increased human deforestation fires and associated escape fires (i.e., degradation fires) in the tropical humid forests, even though the decrease in burned area in many other regions due to human fire suppression acts to increase land carbon gain. The direct human effect on fire weakens the upward trend in global runoff throughout the century by 6% and enhances the upward trend in global evapotranspiration since ~ 1945 by 7%. In addition, the above impacts in densely populated, highly developed (if population density > 0.1 person/km2), or moderately populated and developed regions are of opposite sign to those in other regions. Our study suggests that particular attention should be paid to human deforestation and degradation fires in the tropical humid forests when reconstructing and projecting fire carbon emissions and net atmosphere-land carbon exchange and estimating resultant impacts of direct human effect on fire.

Algae-Based Carbon Sequestration

Science.gov (United States)

Haoyang, Cai

2018-03-01

Our civilization is facing a series of environmental problems, including global warming and climate change, which are caused by the accumulation of green house gases in the atmosphere. This article will briefly analyze the current global warming problem and propose a method that we apply algae cultivation to absorb carbon and use shellfish to sequestrate it. Despite the importance of decreasing CO2 emissions or developing carbon-free energy sources, carbon sequestration should be a key issue, since the amount of carbon dioxide that already exists in the atmosphere is great enough to cause global warming. Algae cultivation would be a good choice because they have high metabolism rates and provides shellfish with abundant food that contains carbon. Shellfish’s shells, which are difficult to be decomposed, are reliable storage of carbon, compared to dead organisms like trees and algae. The amount of carbon that can be sequestrated by shellfish is considerable. However, the sequestrating rate of algae and shellfish is not high enough to affect the global climate. Research on algae and shellfish cultivation, including gene technology that aims to create “super plants” and “super shellfish”, is decisive to the solution. Perhaps the baton of history will shift to gene technology, from nuclear physics that has lost appropriate international environment after the end of the Cold War. Gene technology is vital to human survival.

Global socioeconomic carbon stocks in long-lived products 1900-2008

Science.gov (United States)

Lauk, Christian; Haberl, Helmut; Erb, Karl-Heinz; Gingrich, Simone; Krausmann, Fridolin

2012-09-01

A better understanding of the global carbon cycle as well as of climate change mitigation options such as carbon sequestration requires the quantification of natural and socioeconomic stocks and flows of carbon. A so-far under-researched aspect of the global carbon budget is the accumulation of carbon in long-lived products such as buildings and furniture. We present a comprehensive assessment of global socioeconomic carbon stocks and the corresponding in- and outflows during the period 1900-2008. These data allowed calculation of the annual carbon sink in socioeconomic stocks during this period. The study covers the most important socioeconomic carbon fractions, i.e. wood, bitumen, plastic and cereals. Our assessment was mainly based on production and consumption data for plastic, bitumen and wood products and the respective fractions remaining in stocks in any given year. Global socioeconomic carbon stocks were 2.3 GtC in 1900 and increased to 11.5 GtC in 2008. The share of wood in total C stocks fell from 97% in 1900 to 60% in 2008, while the shares of plastic and bitumen increased to 16% and 22%, respectively. The rate of gross carbon sequestration in socioeconomic stocks increased from 17 MtC yr-1 in 1900 to a maximum of 247 MtC yr-1 in 2007, corresponding to 2.2%-3.4% of global fossil-fuel-related carbon emissions. We conclude that while socioeconomic carbon stocks are not negligible, their growth over time is not a major climate change mitigation option and there is an only modest potential to mitigate climate change by the increase of socioeconomic carbon stocks.

Deepwater carbonate ion concentrations in the western tropical Pacific since 250 ka: Evidence for oceanic carbon storage and global climate influence

Science.gov (United States)

Qin, Bingbin; Li, Tiegang; Xiong, Zhifang; Algeo, Thomas J.; Chang, Fengming

2017-04-01

We present new "size-normalized weight" (SNW)-Δ[CO32-] core-top calibrations for three planktonic foraminiferal species and assess their reliability as a paleo-alkalinity proxy. SNWs of Globigerina sacculifer and Neogloboquadrina dutertrei can be used to reconstruct past deep Pacific [CO32-], whereas SNWs of Pulleniatina obliquiloculata are controlled by additional environmental factors. Based on this methodological advance, we reconstruct SNW-based deepwater [CO32-] for core WP7 from the western tropical Pacific since 250 ka. Secular variation in the SNW proxy documents little change in deep Pacific [CO32-] between the Last Glacial Maximum and the Holocene. Further back in time, deepwater [CO32-] shows long-term increases from marine isotope stage (MIS) 5e to MIS 3 and from early MIS 7 to late MIS 6, consistent with the "coral reef hypothesis" that the deep Pacific Ocean carbonate system responded to declining shelf carbonate production during these two intervals. During deglaciations, we have evidence of [CO32-] peaks coincident with Terminations 2 and 3, which suggests that a breakdown of oceanic vertical stratification drove a net transfer of CO2 from the ocean to the atmosphere, causing spikes in carbonate preservation (i.e., the "deglacial ventilation hypothesis"). During MIS 4, a transient decline in SNW-based [CO32-], along with other reported [CO32-] and/or dissolution records, implies that increased deep-ocean carbon storage resulted in a global carbonate dissolution event. These findings provide new insights into the role of the deep Pacific in the global carbon cycle during the late Quaternary.

Biomass burning studies and the International Global Atmospheric Chemistry (IGAC) project

Science.gov (United States)

Prinn, Ronald G.

1991-01-01

IGAC is an ambitious, decade-long and global research initiative concerned with major research challenges in the field of atmospheric chemistry; its chemists and ecosystem biologists are addressing the problems associated with global biomass burning (BMB). Among IGAC's goals is the achievement of a fundamental understanding of the natural and anthropogenic processes determining changes in atmospheric composition and chemistry, in order to allow century-long predictions. IGAC's studies have been organized into 'foci', encompassing the marine, tropical, polar, boreal, and midlatitude areas, as well as their global composite interactions. Attention is to be given to the effects of BMB on biogeochemical cycles.

ForC: a global database of forest carbon stocks and fluxes.

Science.gov (United States)

Anderson-Teixeira, Kristina J; Wang, Maria M H; McGarvey, Jennifer C; Herrmann, Valentine; Tepley, Alan J; Bond-Lamberty, Ben; LeBauer, David S

2018-06-01

Forests play an influential role in the global carbon (C) cycle, storing roughly half of terrestrial C and annually exchanging with the atmosphere more than five times the carbon dioxide (CO 2 ) emitted by anthropogenic activities. Yet, scaling up from field-based measurements of forest C stocks and fluxes to understand global scale C cycling and its climate sensitivity remains an important challenge. Tens of thousands of forest C measurements have been made, but these data have yet to be integrated into a single database that makes them accessible for integrated analyses. Here we present an open-access global Forest Carbon database (ForC) containing previously published records of field-based measurements of ecosystem-level C stocks and annual fluxes, along with disturbance history and methodological information. ForC expands upon the previously published tropical portion of this database, TropForC (https://doi.org/10.5061/dryad.t516f), now including 17,367 records (previously 3,568) representing 2,731 plots (previously 845) in 826 geographically distinct areas. The database covers all forested biogeographic and climate zones, represents forest stands of all ages, and currently includes data collected between 1934 and 2015. We expect that ForC will prove useful for macroecological analyses of forest C cycling, for evaluation of model predictions or remote sensing products, for quantifying the contribution of forests to the global C cycle, and for supporting international efforts to inventory forest carbon and greenhouse gas exchange. A dynamic version of ForC is maintained at on GitHub (https://GitHub.com/forc-db), and we encourage the research community to collaborate in updating, correcting, expanding, and utilizing this database. ForC is an open access database, and we encourage use of the data for scientific research and education purposes. Data may not be used for commercial purposes without written permission of the database PI. Any publications using For

Impacts of climate mitigation strategies in the energy sector on global land use and carbon balance

Science.gov (United States)

Engström, Kerstin; Lindeskog, Mats; Olin, Stefan; Hassler, John; Smith, Benjamin

2017-09-01

Reducing greenhouse gas emissions to limit damage to the global economy climate-change-induced and secure the livelihoods of future generations requires ambitious mitigation strategies. The introduction of a global carbon tax on fossil fuels is tested here as a mitigation strategy to reduce atmospheric CO2 concentrations and radiative forcing. Taxation of fossil fuels potentially leads to changed composition of energy sources, including a larger relative contribution from bioenergy. Further, the introduction of a mitigation strategy reduces climate-change-induced damage to the global economy, and thus can indirectly affect consumption patterns and investments in agricultural technologies and yield enhancement. Here we assess the implications of changes in bioenergy demand as well as the indirectly caused changes in consumption and crop yields for global and national cropland area and terrestrial biosphere carbon balance. We apply a novel integrated assessment modelling framework, combining three previously published models (a climate-economy model, a socio-economic land use model and an ecosystem model). We develop reference and mitigation scenarios based on the narratives and key elements of the shared socio-economic pathways (SSPs). Taking emissions from the land use sector into account, we find that the introduction of a global carbon tax on the fossil fuel sector is an effective mitigation strategy only for scenarios with low population development and strong sustainability criteria (SSP1 Taking the green road). For scenarios with high population growth, low technological development and bioenergy production the high demand for cropland causes the terrestrial biosphere to switch from being a carbon sink to a source by the end of the 21st century.

Impacts of climate mitigation strategies in the energy sector on global land use and carbon balance

Directory of Open Access Journals (Sweden)

K. Engström

2017-09-01

Full Text Available Reducing greenhouse gas emissions to limit damage to the global economy climate-change-induced and secure the livelihoods of future generations requires ambitious mitigation strategies. The introduction of a global carbon tax on fossil fuels is tested here as a mitigation strategy to reduce atmospheric CO2 concentrations and radiative forcing. Taxation of fossil fuels potentially leads to changed composition of energy sources, including a larger relative contribution from bioenergy. Further, the introduction of a mitigation strategy reduces climate-change-induced damage to the global economy, and thus can indirectly affect consumption patterns and investments in agricultural technologies and yield enhancement. Here we assess the implications of changes in bioenergy demand as well as the indirectly caused changes in consumption and crop yields for global and national cropland area and terrestrial biosphere carbon balance. We apply a novel integrated assessment modelling framework, combining three previously published models (a climate–economy model, a socio-economic land use model and an ecosystem model. We develop reference and mitigation scenarios based on the narratives and key elements of the shared socio-economic pathways (SSPs. Taking emissions from the land use sector into account, we find that the introduction of a global carbon tax on the fossil fuel sector is an effective mitigation strategy only for scenarios with low population development and strong sustainability criteria (SSP1 Taking the green road. For scenarios with high population growth, low technological development and bioenergy production the high demand for cropland causes the terrestrial biosphere to switch from being a carbon sink to a source by the end of the 21st century.

Black carbon in the atmosphere and snow, from pre-industrial times until present

Directory of Open Access Journals (Sweden)

R. B. Skeie

2011-07-01

Full Text Available The distribution of black carbon (BC in the atmosphere and the deposition of BC on snow surfaces since pre-industrial time until present are modelled with the Oslo CTM2 model. The model results are compared with observations including recent measurements of BC in snow in the Arctic. The global mean burden of BC from fossil fuel and biofuel sources increased during two periods. The first period, until 1920, is related to increases in emissions in North America and Europe, and the last period after 1970 are related mainly to increasing emissions in East Asia. Although the global burden of BC from fossil fuel and biofuel increases, in the Arctic the maximum atmospheric BC burden as well as in the snow was reached in 1960s, with a slight reduction thereafter. The global mean burden of BC from open biomass burning sources has not changed significantly since 1900. With current inventories of emissions from open biomass sources, the modelled burden of BC in snow and in the atmosphere north of 65° N is small compared to the BC burden of fossil fuel and biofuel origin. From the concentration changes radiative forcing time series due to the direct aerosol effect as well as the snow-albedo effect is calculated for BC from fossil fuel and biofuel. The calculated radiative forcing in 2000 for the direct aerosol effect is 0.35 W m⁻² and for the snow-albedo effect 0.016 W m⁻² in this study. Due to a southward shift in the emissions there is an increase in the lifetime of BC as well as an increase in normalized radiative forcing, giving a change in forcing per unit of emissions of 26 % since 1950.

Photosynthesis-dependent isoprene emission from leaf to planet in a global carbon-chemistry-climate model

Science.gov (United States)

Unger, N.; Harper, K.; Zheng, Y.; Kiang, N. Y.; Aleinov, I.; Arneth, A.; Schurgers, G.; Amelynck, C.; Goldstein, A.; Guenther, A.; Heinesch, B.; Hewitt, C. N.; Karl, T.; Laffineur, Q.; Langford, B.; McKinney, K. A.; Misztal, P.; Potosnak, M.; Rinne, J.; Pressley, S.; Schoon, N.; Serça, D.

2013-10-01

We describe the implementation of a biochemical model of isoprene emission that depends on the electron requirement for isoprene synthesis into the Farquhar-Ball-Berry leaf model of photosynthesis and stomatal conductance that is embedded within a global chemistry-climate simulation framework. The isoprene production is calculated as a function of electron transport-limited photosynthesis, intercellular and atmospheric carbon dioxide concentration, and canopy temperature. The vegetation biophysics module computes the photosynthetic uptake of carbon dioxide coupled with the transpiration of water vapor and the isoprene emission rate at the 30 min physical integration time step of the global chemistry-climate model. In the model, the rate of carbon assimilation provides the dominant control on isoprene emission variability over canopy temperature. A control simulation representative of the present-day climatic state that uses 8 plant functional types (PFTs), prescribed phenology and generic PFT-specific isoprene emission potentials (fraction of electrons available for isoprene synthesis) reproduces 50% of the variability across different ecosystems and seasons in a global database of 28 measured campaign-average fluxes. Compared to time-varying isoprene flux measurements at 9 select sites, the model authentically captures the observed variability in the 30 min average diurnal cycle (R2 = 64-96%) and simulates the flux magnitude to within a factor of 2. The control run yields a global isoprene source strength of 451 TgC yr-1 that increases by 30% in the artificial absence of plant water stress and by 55% for potential natural vegetation.

Photosynthesis-dependent Isoprene Emission from Leaf to Planet in a Global Carbon-chemistry-climate Model

Science.gov (United States)

Unger, N.; Harper, K.; Zeng, Y.; Kiang, N. Y.; Alienov, I.; Arneth, A.; Schurgers, G.; Amelynck, C.; Goldstein, A.; Guenther, A.;

Global controls on carbon storage in mangrove soils

Science.gov (United States)

Rovai, André S.; Twilley, Robert R.; Castañeda-Moya, Edward; Riul, Pablo; Cifuentes-Jara, Miguel; Manrow-Villalobos, Marilyn; Horta, Paulo A.; Simonassi, José C.; Fonseca, Alessandra L.; Pagliosa, Paulo R.

2018-06-01

Global-scale variation in mangrove ecosystem properties has been explained using a conceptual framework linking geomorphological processes to distinct coastal environmental settings (CES) for nearly 50 years. However, these assumptions have not been empirically tested at the global scale. Here, we show that CES account for global variability in mangrove soil C:N:P stoichiometry and soil organic carbon (SOC) stocks. Using this ecogeomorphology framework, we developed a global model that captures variation in mangrove SOC stocks compatible with distinct CES. We show that mangrove SOC stocks have been underestimated by up to 50% (a difference of roughly 200 Mg ha-1) in carbonate settings and overestimated by up to 86% (around 400 Mg ha-1) in deltaic coastlines. Moreover, we provide information for 57 nations that currently lack SOC data, enabling these and other countries to develop or evaluate their blue carbon inventories.

Evidence that global evapotranspiration makes a substantial contribution to the global atmospheric temperature slowdown

Science.gov (United States)

Leggett, L. Mark W.; Ball, David A.

2018-02-01

The difference between the time series trend for temperature expected from the increasing level of atmospheric CO2 and that for the (more slowly rising) observed temperature has been termed the global surface temperature slowdown. In this paper, we characterise the single time series made from the subtraction of these two time series as the `global surface temperature gap'. We also develop an analogous atmospheric CO2 gap series from the difference between the level of CO2 and first-difference CO2 (that is, the change in CO2 from one period to the next). This paper provides three further pieces of evidence concerning the global surface temperature slowdown. First, we find that the present size of both the global surface temperature gap and the CO2 gap is unprecedented over a period starting at least as far back as the 1860s. Second, ARDL and Granger causality analyses involving the global surface temperature gap against the major candidate physical drivers of the ocean heat sink and biosphere evapotranspiration are conducted. In each case where ocean heat data was available, it was significant in the models: however, evapotranspiration, or its argued surrogate precipitation, also remained significant in the models alongside ocean heat. In terms of relative scale, the standardised regression coefficient for evapotranspiration was repeatedly of the same order of magnitude as—typically as much as half that for—ocean heat. The foregoing is evidence that, alongside the ocean heat sink, evapotranspiration is also likely to be making a substantial contribution to the global atmospheric temperature outcome. Third, there is evidence that both the ocean heat sink and the evapotranspiration process might be able to continue into the future to keep the temperature lower than the level-of-CO2 models would suggest. It is shown that this means there can be benefit in using the first-difference CO2 to temperature relationship shown in Leggett and Ball (Atmos Chem Phys 15

Radiations in space and global environment

International Nuclear Information System (INIS)

Oguti, Takasi

1994-01-01

It has been well known that the global environment of the earth is basically determined by the radiation equilibrium of the earth atmosphere system embedded in the solar radiation. However, the surface temperature of about 15 degC on average is much higher than that determined by the radiation equilibrium. This is due to the so-called greenhouse gases in the atmosphere such as carbon dioxide, water vapor, methane and others. Also the global environment has evolved by interacting with the living things on the earth, for example, tree oxygen by photosynthesis, and a small amount of ozone protecting living things from the fetal damage due to solar ultraviolet radiation. The solar radiation of short wavelength, that is, ultraviolet to X-ray influences atmospheric constituents, and the thermal structure and dynamics of the atmosphere through chemical reaction. The solar energetic particles produced by solar flares precipitate in the polar regions, and the nitric oxides are produced by auroral X-ray. Auroral activities accelerate particles in the magnetosphere. All these radiations cause significant global changes. Human activities increase greenhouse gases rapidly and cause global warming, and atmospheric chloro-fluoro-carbon (CFC) makes the ozone hole. Now, human activities must be modified to match the natural cycle of materials. (K.I.)

Long-term decline of global atmospheric ethane concentrations and implications for methane.

Science.gov (United States)

Simpson, Isobel J; Sulbaek Andersen, Mads P; Meinardi, Simone; Bruhwiler, Lori; Blake, Nicola J; Helmig, Detlev; Rowland, F Sherwood; Blake, Donald R

2012-08-23

After methane, ethane is the most abundant hydrocarbon in the remote atmosphere. It is a precursor to tropospheric ozone and it influences the atmosphere's oxidative capacity through its reaction with the hydroxyl radical, ethane's primary atmospheric sink. Here we present the longest continuous record of global atmospheric ethane levels. We show that global ethane emission rates decreased from 14.3 to 11.3 teragrams per year, or by 21 per cent, from 1984 to 2010. We attribute this to decreasing fugitive emissions from ethane's fossil fuel source--most probably decreased venting and flaring of natural gas in oil fields--rather than a decline in its other major sources, biofuel use and biomass burning. Ethane's major emission sources are shared with methane, and recent studies have disagreed on whether reduced fossil fuel or microbial emissions have caused methane's atmospheric growth rate to slow. Our findings suggest that reduced fugitive fossil fuel emissions account for at least 10-21 teragrams per year (30-70 per cent) of the decrease in methane's global emissions, significantly contributing to methane's slowing atmospheric growth rate since the mid-1980s.

Carbon sequestration research and development

Energy Technology Data Exchange (ETDEWEB)

Reichle, Dave; Houghton, John; Kane, Bob; Ekmann, Jim; and others

1999-12-31

Predictions of global energy use in the next century suggest a continued increase in carbon emissions and rising concentrations of carbon dioxide (CO{sub 2}) in the atmosphere unless major changes are made in the way we produce and use energy--in particular, how we manage carbon. For example, the Intergovernmental Panel on Climate Change (IPCC) predicts in its 1995 ''business as usual'' energy scenario that future global emissions of CO{sub 2} to the atmosphere will increase from 7.4 billion tonnes of carbon (GtC) per year in 1997 to approximately 26 GtC/year by 2100. IPCC also projects a doubling of atmospheric CO{sub 2} concentration by the middle of next century and growing rates of increase beyond. Although the effects of increased CO{sub 2} levels on global climate are uncertain, many scientists agree that a doubling of atmospheric CO{sub 2} concentrations could have a variety of serious environmental consequences. The goal of this report is to identify key areas for research and development (R&D) that could lead to an understanding of the potential for future use of carbon sequestration as a major tool for managing carbon emissions. Under the leadership of DOE, researchers from universities, industry, other government agencies, and DOE national laboratories were brought together to develop the technical basis for conceiving a science and technology road map. That effort has resulted in this report, which develops much of the information needed for the road map.

Development of a Ground-Based Atmospheric Monitoring Network for the Global Mercury Observation System (GMOS

Directory of Open Access Journals (Sweden)

Sprovieri F.

2013-04-01

Full Text Available Consistent, high-quality measurements of atmospheric mercury (Hg are necessary in order to better understand Hg emissions, transport, and deposition on a global scale. Although the number of atmospheric Hg monitoring stations has increased in recent years, the available measurement database is limited and there are many regions of the world where measurements have not been extensively performed. Long-term atmospheric Hg monitoring and additional ground-based monitoring sites are needed in order to generate datasets that will offer new insight and information about the global scale trends of atmospheric Hg emissions and deposition. In the framework of the Global Mercury Observation System (GMOS project, a coordinated global observational network for atmospheric Hg is being established. The overall research strategy of GMOS is to develop a state-of-the-art observation system able to provide information on the concentration of Hg species in ambient air and precipitation on the global scale. This network is being developed by integrating previously established ground-based atmospheric Hg monitoring stations with newly established GMOS sites that are located both at high altitude and sea level locations, as well as in climatically diverse regions. Through the collection of consistent, high-quality atmospheric Hg measurement data, we seek to create a comprehensive assessment of atmospheric Hg concentrations and their dependence on meteorology, long-range atmospheric transport and atmospheric emissions.

Estimating Terrestrial Wood Biomass from Observed Concentrations of Atmospheric Carbon Dioxide

NARCIS (Netherlands)

Schaefer, K. M.; Peters, W.; Carvalhais, N.; van der Werf, G.; Miller, J.

2008-01-01

We estimate terrestrial disequilibrium state and wood biomass from observed concentrations of atmospheric CO2 using the CarbonTracker system coupled to the SiBCASA biophysical model. Starting with a priori estimates of carbon flux from the land, ocean, and fossil fuels, CarbonTracker estimates net

GIS based approach for atmospheric carbon absorption strategies through forests development in Indian situations

International Nuclear Information System (INIS)

Yadav, Surendra Kumar

2013-01-01

Geographical information system (GIS) play important role in forest management. An effective strategy for enhancement of atmospheric carbon absorption productivity is through forests development in degraded forest areas and waste lands. Forestry sector has significant emissions removal capability which can further be enhanced by operationalizing major afforestation and reforestation initiatives like National Mission for a Green India besides continued strengthening of the present protection regime of forests. Secondary data was collected and analyzed. Different types of waste lands require different strategies for their development into forest areas; but few waste lands like rocky regions, glacier regions etc. cannot be developed into forest areas. Atmospheric carbon management is major problem before world community in present circumstances to control environmental pollution. Various forest ecosystems play significant role in carbon absorption. The diffusional net absorption rate of anthropogenic carbon to the biosphere is some unknown function of the atmospheric partial pressure of carbon dioxide. Estimations reveal that the average carbon absorption of the forests was around 1,240 grams (1.240 Kg) of carbon per square meter of canopy area. To stabilize atmospheric CO 2 , role of forestry depends on harvesting and disturbance rates, expectations of future forest productivity, and the ability to deploy technology and forest practices to increase the retention of sequestered CO 2 . There is a considerable self-damping effect that will moderate the future increase of the atmospheric carbon dioxide concentration. Capacity of the ocean to absorb carbon dioxide is limited; but atmospheric carbon absorption potentiality of India forests can be increased tremendously through reforestation, afforestation and development of degraded forest areas and waste lands. About 60 % of Indian waste lands can be developed to increase forest cover with reasonable efforts. When

GIS based approach for atmospheric carbon absorption strategies through forests development in Indian situations

Energy Technology Data Exchange (ETDEWEB)

Yadav, Surendra Kumar [CCS Univ., Meerut (India). SCRIET

2013-07-01

Geographical information system (GIS) play important role in forest management. An effective strategy for enhancement of atmospheric carbon absorption productivity is through forests development in degraded forest areas and waste lands. Forestry sector has significant emissions removal capability which can further be enhanced by operationalizing major afforestation and reforestation initiatives like National Mission for a Green India besides continued strengthening of the present protection regime of forests. Secondary data was collected and analyzed. Different types of waste lands require different strategies for their development into forest areas; but few waste lands like rocky regions, glacier regions etc. cannot be developed into forest areas. Atmospheric carbon management is major problem before world community in present circumstances to control environmental pollution. Various forest ecosystems play significant role in carbon absorption. The diffusional net absorption rate of anthropogenic carbon to the biosphere is some unknown function of the atmospheric partial pressure of carbon dioxide. Estimations reveal that the average carbon absorption of the forests was around 1,240 grams (1.240 Kg) of carbon per square meter of canopy area. To stabilize atmospheric CO{sub 2}, role of forestry depends on harvesting and disturbance rates, expectations of future forest productivity, and the ability to deploy technology and forest practices to increase the retention of sequestered CO{sub 2}. There is a considerable self-damping effect that will moderate the future increase of the atmospheric carbon dioxide concentration. Capacity of the ocean to absorb carbon dioxide is limited; but atmospheric carbon absorption potentiality of India forests can be increased tremendously through reforestation, afforestation and development of degraded forest areas and waste lands. About 60 % of Indian waste lands can be developed to increase forest cover with reasonable efforts. When

ATOMIC CARBON IN THE UPPER ATMOSPHERE OF TITAN

International Nuclear Information System (INIS)

Zhang, X.; Yung, Y. L.; Ajello, J. M.

2010-01-01

The atomic carbon emission C I line feature at 1657 A ( 3 P 0 J - 3 P J ) in the upper atmosphere of Titan is first identified from the airglow spectra obtained by the Cassini Ultra-violet Imaging Spectrograph. A one-dimensional photochemical model of Titan is used to study the photochemistry of atomic carbon on Titan. Reaction between CH and atomic hydrogen is the major source of atomic carbon, and reactions with hydrocarbons (C 2 H 2 and C 2 H 4 ) are the most important loss processes. Resonance scattering of sunlight by atomic carbon is the dominant emission mechanism. The emission intensity calculations based on model results show good agreement with the observations.

Stable isotope composition of atmospheric carbon monoxide. A modelling study

International Nuclear Information System (INIS)

Gromov, Sergey S.

2014-01-01

This study aims at an improved understanding of the stable carbon and oxygen isotope composition of the carbon monoxide (CO) in the global atmosphere by means of numerical simulations. At first, a new kinetic chemistry tagging technique for the most complete parameterisation of isotope effects has been introduced into the Modular Earth Submodel System (MESSy) framework. Incorporated into the ECHAM/MESSy Atmospheric Chemistry (EMAC) general circulation model, an explicit treatment of the isotope effects on the global scale is now possible. The expanded model system has been applied to simulate the chemical system containing up to five isotopologues of all carbon- and oxygen-bearing species, which ultimately determine the δ 13 C, δ 18 O and Δ 17 O isotopic signatures of atmospheric CO. As model input, a new stable isotope-inclusive emission inventory for the relevant trace gases has been compiled. The uncertainties of the emission estimates and of the resulting simulated mixing and isotope ratios have been analysed. The simulated CO mixing and stable isotope ratios have been compared to in-situ measurements from ground-based observatories and from the civil-aircraft-mounted CARIBIC-1 measurement platform. The systematically underestimated 13 CO/ 12 CO ratios of earlier, simplified modelling studies can now be partly explained. The EMAC simulations do not support the inferences of those studies, which suggest for CO a reduced input of the highly depleted in 13 C methane oxidation source. In particular, a high average yield of 0.94 CO per reacted methane (CH 4 ) molecule is simulated in the troposphere, to a large extent due to the competition between the deposition and convective transport processes affecting the CH 4 to CO reaction chain intermediates. None of the other factors, assumed or disregarded in previous studies, however hypothesised to have the potential in enriching tropospheric CO in 13 C, were found significant when explicitly simulated. The

Precipitation and Carbon-Water Coupling Jointly Control the Interannual Variability of Global Land Gross Primary Production

Science.gov (United States)

Zhang, Yao; Xiao, Xiangming; Guanter, Luis; Zhou, Sha; Ciais, Philippe; Joiner, Joanna; Sitch, Stephen; Wu, Xiaocui; Nabel, Julian; Dong, Jinwei;

Toward GEOS-6, A Global Cloud System Resolving Atmospheric Model

Science.gov (United States)

Putman, William M.

2010-01-01

NASA is committed to observing and understanding the weather and climate of our home planet through the use of multi-scale modeling systems and space-based observations. Global climate models have evolved to take advantage of the influx of multi- and many-core computing technologies and the availability of large clusters of multi-core microprocessors. GEOS-6 is a next-generation cloud system resolving atmospheric model that will place NASA at the forefront of scientific exploration of our atmosphere and climate. Model simulations with GEOS-6 will produce a realistic representation of our atmosphere on the scale of typical satellite observations, bringing a visual comprehension of model results to a new level among the climate enthusiasts. In preparation for GEOS-6, the agency's flagship Earth System Modeling Framework [JDl] has been enhanced to support cutting-edge high-resolution global climate and weather simulations. Improvements include a cubed-sphere grid that exposes parallelism; a non-hydrostatic finite volume dynamical core, and algorithm designed for co-processor technologies, among others. GEOS-6 represents a fundamental advancement in the capability of global Earth system models. The ability to directly compare global simulations at the resolution of spaceborne satellite images will lead to algorithm improvements and better utilization of space-based observations within the GOES data assimilation system

Global warming and climate change: control methods

International Nuclear Information System (INIS)

Laal, M.; Aliramaie, A.

2008-01-01

This paper aimed at finding causes of global warming and ways to bring it under control. Data based on scientific opinion as given by synthesis reports of news, articles, web sites, and books. global warming is the observed and projected increases in average temperature of Earth's atmosphere and oceans. Carbon dioxide and other air pollution that is collecting in the atmosphere like a thickening blanket, trapping the sun's heat and causing the planet to warm up. Pollution is one of the biggest man-made problems. Burning fossil fuels is the main factor of pollution. As average temperature increases, habitats, species and people are threatened by drought, changes in rainfall, altered seasons, and more violent storms and floods. Indeed the life cycle of nuclear power results in relatively little pollution. Energy efficiency, solar, wind and other renewable fuels are other weapons against global warming . Human activity, primarily burning fossil fuels, is the major driving factor in global warming . Curtailing the release of carbon dioxide into the atmosphere by reducing use of oil, gasoline, coal and employment of alternate energy, sources are the tools for keeping global warming under control. global warming can be slowed and stopped, with practical actions thal yield a cleaner, healthier atmosphere

Global and regional effects of land-use change on climate in 21. century simulations with interactive carbon cycle

International Nuclear Information System (INIS)

Boysen, L.R.; Brovkin, V.; Pongratz, J.; Gayler, V.; Arora, V.K.; Cadule, P.; Noblet-Ducoudre, N. de; Kato, E.

2014-01-01

Bio-geophysical (BGP) and biogeochemical (BGC) effects of land-use and land cover change (LULCC) are separated at the global and regional scales in new interactive CO 2 simulations for the 21. century. Results from four earth system models (ESMs) are analyzed for the future RCP8.5 scenario from simulations with and without land-use and land cover change (LULCC), contributing to the Land-Use and Climate, Identification of robust impacts (LUCID) project. Over the period 2006-2100, LULCC causes the atmospheric CO 2 concentration to increase by 12, 22, and 66 ppm in CanESM2, MIROC-ESM, and MPI-ESM-LR, respectively. Statistically significant changes in global near-surface temperature are found in three models with a BGC induced global mean annual warming between 0.07 and 0.23 K. BGP-induced responses are simulated by three models in areas of intense LULCC of varying sign and magnitude (between -0.47 and 0.10 K). Modifications of the land carbon pool by LULCC are disentangled in accordance with processes that can lead to increases and decreases in this carbon pool. Global land carbon losses due to LULCC are simulated by all models: 218, 57, 35 and 34 Gt C by MPI-ESM-LR, MIROC-ESM, IPSL-CM5A-LR and CanESM2, respectively. On the contrary, the CO 2 -fertilization effect caused by elevated atmospheric CO 2 concentrations due to LULCC leads to a land carbon gain of 39 Gt C in MPI-ESM-LR and is almost negligible in the other models. A substantial part of the spread in models' responses to LULCC is attributed to the differences in implementation of LULCC (e.g., whether pastures or crops are simulated explicitly) and the simulation of specific processes. Simple idealized experiments with clear protocols for implementing LULCC in ESMs are needed to increase the understanding of model responses and the statistical significance of results, especially when analyzing the regional-scale impacts of LULCC. (authors)

Global Carbon-and-Conservation Models, Global Eco-States? Ecuador’s Yasuní-ITT Initiative and Governance Implications

Directory of Open Access Journals (Sweden)

Conny Davidsen

2013-05-01

Full Text Available The “global carbon age” marks a structural change far beyond the economic realms of implementing carbon trade, affecting the fabric of global environmental governance and its actors. Carbon trade and conservation in the Global South have taken on various forms, and climate change mitigation efforts in light of continued rainforest deforestation are scrambling to establish effective approaches. Ecuador’s Yasuní-ITT Initiative proposes a new global carbon-and-conservation model in the Ecuadorian Amazon that leaves oil reserves of the Yasuní Ishpingo Tambococha Tiputini (ITT oil fields underground, in exchange for international compensation payments that would be based on voluntary contributions of governments and nongovernmental actors in an international conservation partnership and trust fund under the auspices of the United Nations Development Programme. This model suggests far-reaching consequences, as it introduces new global scales for the sharing and management of environmental costs within a framework of neoliberal cost internalization. The analysis in this paper uses the concept of the “ecological state” (Duit, 2008 as a theoretical point of departure to examine the trans-scalar implications of such a carbon-and-conservation model on global governance structures toward a “global ecological state” (or global eco-state.

PFS/Mars Express first results: water vapour and carbon monoxide global distribution

Science.gov (United States)

Ignatiev, N. I.; Titov, D. V.; Formisano, V.; Moroz, V. I.; Lellouch, E.; Encrenaz, Th.; Fouchet, T.; Grassi, D.; Giuranna, M.; Atreya, S.; Pfs Team

Planetary Fourier Spectrometer onboard Mars Express, with its wide spectral range (1.2--45 um) and high spectral resolution (1.4 cm-1), makes it possible to study in a self-consistent manner the Martian atmosphere by means of simultaneous analysis of spectral features in several spectral regions. As concerned small species, we observe 30--50, 6.3, 2.56, 1.87 and 1.38 μ m H2O bands, and 4.7 and 2.35 μ m CO bands. The most favourable, with respect to the instrument performance, 2.56 μ m H2O and 4.7 μ m CO bands, are used to study the variations of column abundance of water vapour and carbon monoxide on a global scale from pole to pole. All necessary atmospheric parameters, namely temperature profiles, surface pressure, and dust density are obtained from the same spectra, whenever possible.

Lightning-produced Carbon Species in the Atmosphere of Saturn

Science.gov (United States)

Delitsky, Mona; Baines, K. H.

2010-10-01

Recent studies by Baines et al (2009) indicate that thunderstorm-associated clouds on Saturn are spectrally dark from 0.7 to 4 um, darker than regular clouds. This darkening is found to be consistent with the presence of particles of elemental carbon, such as in the form of soot particles mixed in with spectrally bright condensates. This carbon is thought to be generated by lightning-induced dissociation of methane. Lightning on Saturn will input large amounts of energy to a narrow column of atmosphere and generate products at high energies such as radicals and ions. After the column cools down, the new chemical species recombine and are frozen into a new chemical equilibrium. Experimental studies in the literature of reactions of methane and other gases in plasma discharges (which simulate lightning) indicate that, even with high ratios of hydrogen/methane, the elemental carbon obtained will form solid dark particles that persist and have a very high C/H ratio. Basically, they are mostly pure carbon, in the form of soot, amorphous carbon, graphite, graphene, polycyclic aromatic hydrocarbons, carbon black, carbon onions, etc. Hydrogen will act as a sealant onto the particles and attach to dangling bonds on their growing surfaces. Even in experiments to form the most crystalline allotrope of carbon, that is, diamond, the presence of hydrogen does not inhibit diamond formation, even at the low pressures in the atmospheres of the Jovian planets or in the interstellar medium (Allamandola et al 1991). Therefore, some form of elemental carbon is likely produced in Saturnian storm clouds and may occur as dark particles of either amorphous carbon, PAHs or crystalline carbon in a form such as graphite. ..Refs: Baines et al., PSS 57, 1650-1658 (2009) ; Allamandola et al., Meteoritics 26, 313 (1991).

Trends of 13C/12C ratios in pinyon tree rings of the American Southwest and the global carbon cycle

International Nuclear Information System (INIS)

Leavitt, S.W.; Long, A.

1986-01-01

An accurate atmospheric 13 C/ 12 C chronology can provide important constraints to models of the global carbon cycle. Trees accumulate carbon from atmospheric CO 2 into growth rings and offer potential for 13 C/ 12 C reconstructions, but results have not been reproducible. This paper presents δ 13 C curves from 5 sites, representing 20 pinyon (Pinus edulis) trees, where cores of 4 trees from each site have been pooled into a composite sample. Isotopic analysis of cellulose in 5-yr ring groups produces curves with a general trend of decreasing δ 13 C after 1800, but with pronounced short-term fluctuations superimposed upon the trend. Evidence indicates the fluctuations are strongly related to moisture availability (drought). A mean curve of the 5 δ 13 C chronologies from which the fossil-fuel component is subtracted suggests a substantial biospheric CO 2 contribution to the atmosphere since 1800

Centennial evolution of the atmospheric methane budget: what do the carbon isotopes tell us?

Directory of Open Access Journals (Sweden)

K. R. Lassey

2007-01-01

Full Text Available Little is known about how the methane source inventory and sinks have evolved over recent centuries. New and detailed records of methane mixing ratio and isotopic composition (12CH4, 13CH4 and 14CH4 from analyses of air trapped in polar ice and firn can enhance this knowledge. We use existing bottom-up constructions of the source history, including "EDGAR"-based constructions, as inputs to a model of the evolving global budget for methane and for its carbon isotope composition through the 20th century. By matching such budgets to atmospheric data, we examine the constraints imposed by isotope information on those budget evolutions. Reconciling both 12CH4 and 13CH4 budgets with EDGAR-based source histories requires a combination of: a greater proportion of emissions from biomass burning and/or of fossil methane than EDGAR constructions suggest; a greater contribution from natural such emissions than is commonly supposed; and/or a significant role for active chlorine or other highly-fractionating tropospheric sink as has been independently proposed. Examining a companion budget evolution for 14CH4 exposes uncertainties in inferring the fossil-methane source from atmospheric 14CH4 data. Specifically, methane evolution during the nuclear era is sensitive to the cycling dynamics of "bomb 14C" (originating from atmospheric weapons tests through the biosphere. In addition, since ca. 1970, direct production and release of 14CH4 from nuclear-power facilities is influential but poorly quantified. Atmospheric 14CH4 determinations in the nuclear era have the potential to better characterize both biospheric carbon cycling, from photosynthesis to methane synthesis, and the nuclear-power source.

Impacts of continental arcs on global carbon cycling and climate

Science.gov (United States)

Lee, C. T.; Jiang, H.; Carter, L.; Dasgupta, R.; Cao, W.; Lackey, J. S.; Lenardic, A.; Barnes, J.; McKenzie, R.

2017-12-01

On myr timescales, climatic variability is tied to variations in atmospheric CO2, which in turn is driven by geologic sources of CO2 and modulated by the efficiency of chemical weathering and carbonate precipitation (sinks). Long-term variability in CO2 has largely been attributed to changes in mid-ocean ridge inputs or the efficiency of global weathering. For example, the Cretaceous greenhouse is thought to be related to enhanced oceanic crust production, while the late Cenozoic icehouse is attributed to enhanced chemical weathering associated with the Himalayan orogeny. Here, we show that continental arcs may play a more important role in controlling climate, both in terms of sources and sinks. Continental arcs differ from island arcs and mid-ocean ridges in that the continental plate through which arc magmas pass may contain large amounts of sedimentary carbonate, accumulated over the history of the continent. Interaction of arc magmas with crustal carbonates via assimilation, reaction or heating can significantly add to the mantle-sourced CO2 flux. Detrital zircons and global mapping of basement rocks shows that the length of continental arcs in the Cretaceous was more than twice that in the mid-Cenozoic; maps also show many of these arcs intersected crustal carbonates. The increased length of continental arc magmatism coincided with increased oceanic spreading rates, placing convergent margins into compression, which favors continental arcs. Around 50 Ma, however, nearly all the continental arcs in Eurasia and North America terminated as India collided with Eurasia and the western Pacific rolled back, initiating the Marianas-Tonga-Kermadec intra-oceanic subduction complex and possibly leading to a decrease in global CO2 production. Meanwhile, extinct continental arcs continued to erode, resulting in regionally enhanced chemical weathering unsupported by magmatic fluxes of CO2. Continental arcs, during their magmatic lifetimes, are thus a source of CO2, driving

Carbon dioxide and future climate

Energy Technology Data Exchange (ETDEWEB)

Mitchell, J M

1977-03-01

The addition of carbon dioxide to the atmosphere due to burning fossil fuel is discussed. The release rate of carbon dioxide has been growing since at least 1950 at an average rate of 4.3% per year. If all known fossil fuel reserves in the world are consumed, a total of between 5 and 14 times the present amount of carbon dioxide in the atmosphere will be released. The oceans would then be unlikely to withdraw the proportion of perhaps 40% which they are believed to have withdrawn up to the present. The increase in the atmosphere would be in excess of 3 times or conceivably ten times the present amount. If the reserves are used up within a few hundred years, more than half the excess carbon dioxide would remain in the atmosphere after a thousand years. The ''greenhouse'' effect of carbon dioxide is explained. The simulation with numerical models of the effects of carbon dioxide on atmospheric radiation fluxes is discussed. An estimated increase in the average annual temperature of the earth of 2.4 to 2.9C is given for doubling the carbon dioxide content; also a 7% increase in global average precipitation. The effect of increasing carbon dioxide on global mean temperature is viewed in the perspective of the glacial-interglacial cycles. The warming effect of carbon dioxide may induce a ''super-interglacial'' on the present interglacial which is expected to decline toward a new ice age in the next several thousand years. Finally it is proposed that it may be necessary to phase out the use of fossil fuels before all the knowledge is acquired which would necessitate such an action.

A review of the role of temperate forests in the global CO2 balance

International Nuclear Information System (INIS)

Musselman, R.C.; Fox, D.G.

1991-01-01

The role of temperate forests in the global carbon balance is difficult to determine because many uncertainties exist in the data, and many assumptions must be made in these determinations. Still, there is little doubt that increases in atmospheric CO 2 and global warming would have major effects on temperate forest ecosystems. Increases in atmospheric CO 2 may result in increases in photosynthesis, changes in water and nitrogen use efficiency, and changes in carbon allocation. Indirect effects of changes in global carbon balance on regional climate and on microenvironmental conditions, particularly temperature and moisture, may be more important then direct effects of increased CO 2 on vegetation. Increased incidence of forest perturbations might also be expected. The evidence suggests that conditions favorable to forest growth and development may exist in the northern latitudes, while southern latitude forests may undergo drought stress. Current harvest of temperate and world forests contributes substantial amounts of carbon to the atmosphere, possibly as much as 3 gigatons (Gt) per year. Return of this carbon to forest storage may require decades. Forest managers should be aware of the global as well as local impact their management decisions will have on the atmospheric carbon balance of the ecosystems they oversee

Regional forecasting with global atmospheric models

International Nuclear Information System (INIS)

Crowley, T.J.; North, G.R.; Smith, N.R.

1994-05-01

The scope of the report is to present the results of the fourth year's work on the atmospheric modeling part of the global climate studies task. The development testing of computer models and initial results are discussed. The appendices contain studies that provide supporting information and guidance to the modeling work and further details on computer model development. Complete documentation of the models, including user information, will be prepared under separate reports and manuals

Global carbon sequestration in tidal, saline wetland soils

Science.gov (United States)

Chmura, G.L.; Anisfeld, S.C.; Cahoon, D.R.; Lynch, J.C.

2003-01-01

Wetlands represent the largest component of the terrestrial biological carbon pool and thus play an important role in global carbon cycles. Most global carbon budgets, however, have focused on dry land ecosystems that extend over large areas and have not accounted for the many small, scattered carbon-storing ecosystems such as tidal saline wetlands. We compiled data for 154 sites in mangroves and salt marshes from the western and eastern Atlantic and Pacific coasts, as well as the Indian Ocean, Mediterranean Ocean, and Gulf of Mexico. The set of sites spans a latitudinal range from 22.4??S in the Indian Ocean to 55.5??N in the northeastern Atlantic. The average soil carbon density of mangrove swamps (0.055 ?? 0.004 g cm-3) is significantly higher than the salt marsh average (0.039 ?? 0.003 g cm-3). Soil carbon density in mangrove swamps and Spartina patens marshes declines with increasing average annual temperature, probably due to increased decay rates at higher temperatures. In contrast, carbon sequestration rates were not significantly different between mangrove swamps and salt marshes. Variability in sediment accumulation rates within marshes is a major control of carbon sequestration rates masking any relationship with climatic parameters. Globally, these combined wetlands store at least 44.6 Tg C yr-1 and probably more, as detailed areal inventories are not available for salt marshes in China and South America. Much attention has been given to the role of freshwater wetlands, particularly northern peatlands, as carbon sinks. In contrast to peatlands, salt marshes and mangroves release negligible amounts of greenhouse gases and store more carbon per unit area. Copyright 2003 by the American Geophysical Union.

Carbon and environmental footprinting of global biofuel production

OpenAIRE

Hammond, Geoff P.; Seth, S.M.

2013-01-01

The carbon and environmental footprints associated with the global production of biofuels have been computed from a baseline of 2007-2009 out until 2019. Estimates of future global biofuel production were adopted from OECD-FAO and related projections. In order to determine the footprints associated with these (essentially 'first generation') biofuel resources, the overall environmental footprint was disaggregated into bioproductive land, built land, carbon, embodied energy, materials and wast...

Three-pattern decomposition of global atmospheric circulation: part I—decomposition model and theorems

Science.gov (United States)

Hu, Shujuan; Chou, Jifan; Cheng, Jianbo

2018-04-01

In order to study the interactions between the atmospheric circulations at the middle-high and low latitudes from the global perspective, the authors proposed the mathematical definition of three-pattern circulations, i.e., horizontal, meridional and zonal circulations with which the actual atmospheric circulation is expanded. This novel decomposition method is proved to accurately describe the actual atmospheric circulation dynamics. The authors used the NCEP/NCAR reanalysis data to calculate the climate characteristics of those three-pattern circulations, and found that the decomposition model agreed with the observed results. Further dynamical analysis indicates that the decomposition model is more accurate to capture the major features of global three dimensional atmospheric motions, compared to the traditional definitions of Rossby wave, Hadley circulation and Walker circulation. The decomposition model for the first time realized the decomposition of global atmospheric circulation using three orthogonal circulations within the horizontal, meridional and zonal planes, offering new opportunities to study the large-scale interactions between the middle-high latitudes and low latitudes circulations.

Mechanistic modelling of Middle Eocene atmospheric carbon dioxide using fossil plant material

Science.gov (United States)

Grein, Michaela; Roth-Nebelsick, Anita; Wilde, Volker; Konrad, Wilfried; Utescher, Torsten

2010-05-01

Various proxies (such as pedogenic carbonates, boron isotopes or phytoplankton) and geochemical models were applied in order to reconstruct palaeoatmospheric carbon dioxide, partially providing conflicting results. Another promising proxy is the frequency of stomata (pores on the leaf surface used for gaseous exchange). In this project, fossil plant material from the Messel Pit (Hesse, Germany) is used to reconstruct atmospheric carbon dioxide concentration in the Middle Eocene by analyzing stomatal density. We applied the novel mechanistic-theoretical approach of Konrad et al. (2008) which provides a quantitative derivation of the stomatal density response (number of stomata per leaf area) to varying atmospheric carbon dioxide concentration. The model couples 1) C3-photosynthesis, 2) the process of diffusion and 3) an optimisation principle providing maximum photosynthesis (via carbon dioxide uptake) and minimum water loss (via stomatal transpiration). These three sub-models also include data of the palaeoenvironment (temperature, water availability, wind velocity, atmospheric humidity, precipitation) and anatomy of leaf and stoma (depth, length and width of stomatal porus, thickness of assimilation tissue, leaf length). In order to calculate curves of stomatal density as a function of atmospheric carbon dioxide concentration, various biochemical parameters have to be borrowed from extant representatives. The necessary palaeoclimate data are reconstructed from the whole Messel flora using Leaf Margin Analysis (LMA) and the Coexistence Approach (CA). In order to obtain a significant result, we selected three species from which a large number of well-preserved leaves is available (at least 20 leaves per species). Palaeoclimate calculations for the Middle Eocene Messel Pit indicate a warm and humid climate with mean annual temperature of approximately 22°C, up to 2540 mm mean annual precipitation and the absence of extended periods of drought. Mean relative air

Toward Reducing Uncertainties in Biospheric Carbon Uptake in the American West: An Atmospheric Perspective

Science.gov (United States)

Lin, J. C.; Stephens, B. B.; Mallia, D.; Wu, D.; Jacobson, A. R.

2015-12-01

Despite the need for an understanding of terrestrial biospheric carbon fluxes to account for carbon cycle feedbacks and predict future CO2 concentrations, knowledge of such fluxes at the regional scale remains poor. This is particularly true in mountainous areas, where lack of observations combined with difficulties in their interpretation lead to significant uncertainties. Yet mountainous regions are also where significant forest cover and biomass are found—areas that have the potential to serve as carbon sinks. In particular, understanding carbon fluxes in the American West is of critical importance for the U.S. carbon budget, as the large area and biomass indicate potential for carbon sequestration. However, disturbances such as drought, insect outbreak, and wildfires in this region can introduce significant perturbations to the carbon cycle and thereby affect the amount of carbon sequestered by vegetation in the Rockies. To date, there have been few atmospheric CO2 observations in the American Rockies due to a combination of difficulties associated with logistics and interpretation of the measurements in the midst of complex terrain. Among the few sites are those associated with NCAR's Regional Atmospheric Continuous CO2 Network in the Rocky Mountains (Rocky RACCOON). As CO2 observations in mountainous areas increase in the future, it is imperative that they can be properly interpreted to yield information about biospheric carbon fluxes. In this paper, we will present CO2 observations from RACCOON, along with atmospheric simulations that attempt to extract information about biospheric carbon fluxes in the Western U.S. from these observations. We show that atmospheric models can significantly misinterpret the CO2 observations, leading to large errors in the retrieved biospheric fluxes, due to erroneous atmospheric flows. Recommendations for ways to minimize such errors and properly link the CO2 concentrations to biospheric fluxes are discussed.

ISLSCP II Atmospheric Carbon Dioxide Consumption by Continental Erosion

Data.gov (United States)

National Aeronautics and Space Administration — ABSTRACT: The Continental Atmospheric CO2 Consumption data set represents gridded estimates for the riverine export of carbon and of sediments based on empirical...

Carbon inventories and atmospheric temperatures: A global and regional perspective

Digital Repository Service at National Institute of Oceanography (India)

DileepKumar, M.

stream_size 3 stream_content_type text/plain stream_name Proc_Natl_Conf_Global_Temp_Rise_2007_133.pdf.txt stream_source_info Proc_Natl_Conf_Global_Temp_Rise_2007_133.pdf.txt Content-Encoding ISO-8859-1 Content-Type text...

Fiscal federalism approach for controlling global environmental pollution

International Nuclear Information System (INIS)

Murty, M.N.

1996-01-01

It is found that optimal international carbon taxes are country specific and we can decompose a tax on a domestically produced carbon-intensive commodity into a revenue tax, a tax to control local atmospheric pollution and an international carbon tax. It shows that an institutional arrangement for the world economy similar to the fiscal federalism in the federal countries can be useful to internalize the global externalities of atmospheric pollution. 18 refs

A global hybrid coupled model based on atmosphere-SST feedbacks

Energy Technology Data Exchange (ETDEWEB)

Cimatoribus, Andrea A.; Drijfhout, Sybren S. [Royal Netherlands Meteorological Institute, De Bilt (Netherlands); Dijkstra, Henk A. [Utrecht University, Institute for Marine and Atmospheric Research Utrecht, Utrecht (Netherlands)

2012-02-15

A global hybrid coupled model is developed, with the aim of studying the effects of ocean-atmosphere feedbacks on the stability of the Atlantic meridional overturning circulation. The model includes a global ocean general circulation model and a statistical atmosphere model. The statistical atmosphere model is based on linear regressions of data from a fully coupled climate model on sea surface temperature both locally and hemispherically averaged, being the footprint of Atlantic meridional overturning variability. It provides dynamic boundary conditions to the ocean model for heat, freshwater and wind-stress. A basic but consistent representation of ocean-atmosphere feedbacks is captured in the hybrid coupled model and it is more than 10 times faster than the fully coupled climate model. The hybrid coupled model reaches a steady state with a climate close to the one of the fully coupled climate model, and the two models also have a similar response (collapse) of the Atlantic meridional overturning circulation to a freshwater hosing applied in the northern North Atlantic. (orig.)

Mars Global Reference Atmospheric Model 2010 Version: Users Guide

Science.gov (United States)

Justh, H. L.

2014-01-01

This Technical Memorandum (TM) presents the Mars Global Reference Atmospheric Model 2010 (Mars-GRAM 2010) and its new features. Mars-GRAM is an engineering-level atmospheric model widely used for diverse mission applications. Applications include systems design, performance analysis, and operations planning for aerobraking, entry, descent and landing, and aerocapture. Additionally, this TM includes instructions on obtaining the Mars-GRAM source code and data files as well as running Mars-GRAM. It also contains sample Mars-GRAM input and output files and an example of how to incorporate Mars-GRAM as an atmospheric subroutine in a trajectory code.

A discussion for stabilization time of carbon steel in atmospheric corrosion

Science.gov (United States)

Zhang, Zong-kai; Ma, Xiao-bing; Cai, Yi-kun

2017-09-01

Stabilization time is an important parameter in long-term prediction of carbon steel corrosion in atmosphere. The range of the stabilization time of carbon steel in atmospheric corrosion has been published in many scientific literatures. However, the results may not precise because engineering experiences is dominant. This paper deals with the recalculation of stabilization time based on ISO CORRAG program, and analyzes the results and makes a comparison to the data mentioned above. In addition, a new thinking to obtain stabilization time will be proposed.

Photosynthesis-dependent isoprene emission from leaf to planet in a global carbon-chemistry-climate model

Directory of Open Access Journals (Sweden)

N. Unger

2013-10-01

Full Text Available We describe the implementation of a biochemical model of isoprene emission that depends on the electron requirement for isoprene synthesis into the Farquhar–Ball–Berry leaf model of photosynthesis and stomatal conductance that is embedded within a global chemistry-climate simulation framework. The isoprene production is calculated as a function of electron transport-limited photosynthesis, intercellular and atmospheric carbon dioxide concentration, and canopy temperature. The vegetation biophysics module computes the photosynthetic uptake of carbon dioxide coupled with the transpiration of water vapor and the isoprene emission rate at the 30 min physical integration time step of the global chemistry-climate model. In the model, the rate of carbon assimilation provides the dominant control on isoprene emission variability over canopy temperature. A control simulation representative of the present-day climatic state that uses 8 plant functional types (PFTs, prescribed phenology and generic PFT-specific isoprene emission potentials (fraction of electrons available for isoprene synthesis reproduces 50% of the variability across different ecosystems and seasons in a global database of 28 measured campaign-average fluxes. Compared to time-varying isoprene flux measurements at 9 select sites, the model authentically captures the observed variability in the 30 min average diurnal cycle (R2 = 64–96% and simulates the flux magnitude to within a factor of 2. The control run yields a global isoprene source strength of 451 TgC yr−1 that increases by 30% in the artificial absence of plant water stress and by 55% for potential natural vegetation.

Global atmospheric particle formation from CERN CLOUD measurements

Science.gov (United States)

Dunne, Eimear M.; Gordon, Hamish; Carslaw, Kenneth S.

2017-04-01

New particle formation (or nucleation) is acknowledged as a significant source of climate-relevant aerosol throughout the atmosphere. However, performing atmospherically relevant nucleation experiments in a laboratory setting is extremely challenging. As a result, until now, the parameterisations used to represent new particle formation in global aerosol models were largely based on in-situ observations or theoretical nucleation models, and usually only represented the binary H2SO4-H2O system. Several different chemicals can affect particle formation rates, even at extremely low trace concentrations, which are technically challenging to measure directly. Nucleation rates also respond to environmental changes in e.g. temperature in a highly non-linear fashion. The CERN CLOUD experiment was designed to provide the most controlled and accurate nucleation rate measurements to date, over the full range of free tropospheric temperatures and down to sulphuric acid concentrations of the order of 105 cm-3. We will present a parameterisation of inorganic nucleation rates for use in global models, based on these measurements, which includes four separate nucleation pathways: binary neutral, binary ion-induced, ternary neutral, and ternary ion-induced. Both inorganic and organic nucleation parameterisations derived from CLOUD measurements have been implemented in the GLOMAP global aerosol model. The parameterisations depend on temperature and on concentrations of sulphuric acid, ammonia, organic vapours, and ions. One of CLOUD's main original goals was to determine the sensitivity of atmospheric aerosol to changes in the nucleation rate over a solar cycle. We will show that, in a present-day atmosphere, the changes in climate-relevant aerosol (in the form of cloud-level cloud condensation nuclei) over a solar cycle are on average about 0.1%, with local changes of less than 1%. In contrast, anthropogenic changes in ammonia since pre-industrial times were estimated to have a

Sensitivity of global and regional terrestrial carbon storage to the direct CO2 effect and climate change based on the CMIP5 model intercomparison.

Science.gov (United States)

Peng, Jing; Dan, Li; Huang, Mei

2014-01-01

Global and regional land carbon storage has been significantly affected by increasing atmospheric CO2 concentration and climate change. Based on fully coupled climate-carbon-cycle simulations from the Coupled Model Intercomparison Project Phase 5 (CMIP5), we investigate sensitivities of land carbon storage to rising atmospheric CO2 concentration and climate change over the world and 21 regions during the 130 years. Overall, the simulations suggest that consistently spatial positive effects of the increasing CO2 concentrations on land carbon storage are expressed with a multi-model averaged value of 1.04 PgC per ppm. The stronger positive values are mainly located in the broad areas of temperate and tropical forest, especially in Amazon basin and western Africa. However, large heterogeneity distributed for sensitivities of land carbon storage to climate change. Climate change causes decrease in land carbon storage in most tropics and the Southern Hemisphere. In these regions, decrease in soil moisture (MRSO) and enhanced drought somewhat contribute to such a decrease accompanied with rising temperature. Conversely, an increase in land carbon storage has been observed in high latitude and altitude regions (e.g., northern Asia and Tibet). The model simulations also suggest that global negative impacts of climate change on land carbon storage are predominantly attributed to decrease in land carbon storage in tropics. Although current warming can lead to an increase in land storage of high latitudes of Northern Hemisphere due to elevated vegetation growth, a risk of exacerbated future climate change may be induced due to release of carbon from tropics.

Sensitivity of global and regional terrestrial carbon storage to the direct CO2 effect and climate change based on the CMIP5 model intercomparison.

Directory of Open Access Journals (Sweden)

Jing Peng

Full Text Available Global and regional land carbon storage has been significantly affected by increasing atmospheric CO2 concentration and climate change. Based on fully coupled climate-carbon-cycle simulations from the Coupled Model Intercomparison Project Phase 5 (CMIP5, we investigate sensitivities of land carbon storage to rising atmospheric CO2 concentration and climate change over the world and 21 regions during the 130 years. Overall, the simulations suggest that consistently spatial positive effects of the increasing CO2 concentrations on land carbon storage are expressed with a multi-model averaged value of 1.04 PgC per ppm. The stronger positive values are mainly located in the broad areas of temperate and tropical forest, especially in Amazon basin and western Africa. However, large heterogeneity distributed for sensitivities of land carbon storage to climate change. Climate change causes decrease in land carbon storage in most tropics and the Southern Hemisphere. In these regions, decrease in soil moisture (MRSO and enhanced drought somewhat contribute to such a decrease accompanied with rising temperature. Conversely, an increase in land carbon storage has been observed in high latitude and altitude regions (e.g., northern Asia and Tibet. The model simulations also suggest that global negative impacts of climate change on land carbon storage are predominantly attributed to decrease in land carbon storage in tropics. Although current warming can lead to an increase in land storage of high latitudes of Northern Hemisphere due to elevated vegetation growth, a risk of exacerbated future climate change may be induced due to release of carbon from tropics.

Increase of carbon cycle feedback with climate sensitivity: results from a coupled climate and carbon cycle model

International Nuclear Information System (INIS)

Govindasamy, B.; Thompson, S.; Mirin, A.; Wickett, M.; Caldeira, K.; Delire, C.

2005-01-01

Coupled climate and carbon cycle modelling studies have shown that the feedback between global warming and the carbon cycle, in particular the terrestrial carbon cycle, could accelerate climate change and result in greater warming. In this paper we investigate the sensitivity of this feedback for year 2100 global warming in the range of 0 to 8 K. Differing climate sensitivities to increased CO 2 content are imposed on the carbon cycle models for the same emissions. Emissions from the SRES A2 scenario are used. We use a fully coupled climate and carbon cycle model, the INtegrated Climate and CArbon model (INCCA), the NCAR/DOE Parallel Climate Model coupled to the IBIS terrestrial biosphere model and a modified OCMIP ocean biogeochemistry model. In our integrated model, for scenarios with year 2100 global warming increasing from 0 to 8 K, land uptake decreases from 47% to 29% of total CO 2 emissions. Due to competing effects, ocean uptake (16%) shows almost no change at all. Atmospheric CO 2 concentration increases are 48% higher in the run with 8 K global climate warming than in the case with no warming. Our results indicate that carbon cycle amplification of climate warming will be greater if there is higher climate sensitivity to increased atmospheric CO 2 content; the carbon cycle feedback factor increases from 1.13 to 1.48 when global warming increases from 3.2 to 8 K

Detecting and Understanding Changing Arctic Carbon Emissions

Science.gov (United States)

Bruhwiler, L.

2017-12-01

Warming in the Arctic has proceeded faster than anyplace on Earth. Our current understanding of biogeochemistry suggests that we can expect feedbacks between climate and carbon in the Arctic. Changes in terrestrial fluxes of carbon can be expected as the Arctic warms, and the vast stores of organic carbon frozen in Arctic soils could be mobilized to the atmosphere, with possible significant impacts on global climate. Quantifying trends in Arctic carbon exchanges is important for policymaking because greater reductions in anthropogenic emissions may be required to meet climate goals. Observations of greenhouse gases in the Arctic and globally have been collected for several decades. Analysis of this data does not currently support significantly changed Arctic emissions of CH4, however it is difficult to detect changes in Arctic emissions because of transport from lower latitudes and large inter-annual variability. Unfortunately, current space-based remote sensing systems have limitations at Arctic latitudes. Modeling systems can help untangle the Arctic budget of greenhouse gases, but they are dependent on underlying prior fluxes, wetland distributions and global anthropogenic emissions. Also, atmospheric transport models may have significant biases and errors. For example, unrealistic near-surface stability can lead to underestimation of emissions in atmospheric inversions. We discuss our current understanding of the Arctic carbon budget from both top-down and bottom-up approaches. We show that current atmospheric inversions agree well on the CH4 budget. On the other hand, bottom-up models vary widely in their predictions of natural emissions, with some models predicting emissions too large to be accommodated by the budget implied by global observations. Large emissions from the shallow Arctic ocean are also inconsistent with atmospheric observations. We also discuss the sensitivity of the current atmospheric network to what is likely small, gradual increases in

Soil Carbon Chemistry and Greenhouse Gas Production in Global Peatlands

Science.gov (United States)

Normand, A. E.; Turner, B. L.; Lamit, L. J.; Smith, A. N.; Baiser, B.; Clark, M. W.; Hazlett, C.; Lilleskov, E.; Long, J.; Grover, S.; Reddy, K. R.

2017-12-01

Peatlands play a critical role in the global carbon cycle because they contain approximately 30% of the 1500 Pg of carbon stored in soils worldwide. However, the stability of these vast stores of carbon is under threat from climate and land-use change, with important consequences for global climate. Ecosystem models predict the impact of peatland perturbation on carbon fluxes based on total soil carbon pools, but responses could vary markedly depending on the chemical composition of soil organic matter. Here we combine experimental and observational studies to quantify the chemical nature and response to perturbation of soil organic matter in peatlands worldwide. We quantified carbon functional groups in a global sample of 125 freshwater peatlands using solid-state 13C nuclear magnetic resonance (NMR) spectroscopy to determine the drivers of molecular composition of soil organic matter. We then incubated a representative subset of the soils under aerobic and anaerobic conditions to determine how organic matter composition influences carbon dioxide (CO2) and methane (CH4) emissions following drainage or flooding. The functional chemistry of peat varied markedly at large and small spatial scales, due to long-term land use change, mean annual temperature, nutrient status, and vegetation, but not pH. Despite this variation, we found predictable responses of greenhouse gas production following drainage based on soil carbon chemistry, defined by a novel Global Peat Stability Index, with greater CO2 and CH4 fluxes from soils enriched in oxygen-containing organic carbon (O-alkyl C) and depleted in aromatic and hydrophobic compounds. Incorporation of the Global Peat Stability Index of peatland organic matter into earth system models and management strategies, which will improve estimates of GHG fluxes from peatlands and ultimately advance management to reduce carbon loss from these sensitive ecosystems.

Dynamics of radioactive lead isotopes in the global environmental atmosphere

International Nuclear Information System (INIS)

Koike, Yuya; Kosako, Toshiso

2006-01-01

Fundamental information of radioactive lead isotopes, which used as the atmospheric tracer in the global environmental atmosphere, is reviewed. Emanation and exhalation of Rn and Tn, parent nuclide, is stated. Some reports on measurement and application of short-lived lead isotopes are reported. Transfer of radioactive lead isotopes in the atmosphere, vertical profiles of radon, thoron, and short-lived lead isotopes for different turbulent mixing conditions, deposition to aerosol, basic processes of Rn decay product behavior in air defining 'unattached' and 'aerosol-attached' activities, seasonal variation of atmospheric 210 Pb concentration at Beijing and Chengdu, seasonal variation of atmospheric 212 Pb concentration at several observation sites in Japan Islands, and variation in the atmospheric concentration of 212 Pb along with SO 2 are shown. (S.Y.)

Global socioeconomic carbon stocks in long-lived products 1900–2008

International Nuclear Information System (INIS)

Lauk, Christian; Haberl, Helmut; Erb, Karl-Heinz; Gingrich, Simone; Krausmann, Fridolin

2012-01-01

A better understanding of the global carbon cycle as well as of climate change mitigation options such as carbon sequestration requires the quantification of natural and socioeconomic stocks and flows of carbon. A so-far under-researched aspect of the global carbon budget is the accumulation of carbon in long-lived products such as buildings and furniture. We present a comprehensive assessment of global socioeconomic carbon stocks and the corresponding in- and outflows during the period 1900–2008. These data allowed calculation of the annual carbon sink in socioeconomic stocks during this period. The study covers the most important socioeconomic carbon fractions, i.e. wood, bitumen, plastic and cereals. Our assessment was mainly based on production and consumption data for plastic, bitumen and wood products and the respective fractions remaining in stocks in any given year. Global socioeconomic carbon stocks were 2.3 GtC in 1900 and increased to 11.5 GtC in 2008. The share of wood in total C stocks fell from 97% in 1900 to 60% in 2008, while the shares of plastic and bitumen increased to 16% and 22%, respectively. The rate of gross carbon sequestration in socioeconomic stocks increased from 17 MtC yr −1 in 1900 to a maximum of 247 MtC yr −1 in 2007, corresponding to 2.2%–3.4% of global fossil-fuel-related carbon emissions. We conclude that while socioeconomic carbon stocks are not negligible, their growth over time is not a major climate change mitigation option and there is an only modest potential to mitigate climate change by the increase of socioeconomic carbon stocks. (letter)

Global and regional effects of land-use change on climate in 21st century simulations with interactive carbon cycle

Directory of Open Access Journals (Sweden)

L. R. Boysen

2014-09-01

Full Text Available Biogeophysical (BGP and biogeochemical (BGC effects of land-use and land cover change (LULCC are separated at the global and regional scales in new interactive CO2 simulations for the 21st century. Results from four earth system models (ESMs are analyzed for the future RCP8.5 scenario from simulations with and without land-use and land cover change (LULCC, contributing to the Land-Use and Climate, IDentification of robust impacts (LUCID project. Over the period 2006–2100, LULCC causes the atmospheric CO2 concentration to increase by 12, 22, and 66 ppm in CanESM2, MIROC-ESM, and MPI-ESM-LR, respectively. Statistically significant changes in global near-surface temperature are found in three models with a BGC-induced global mean annual warming between 0.07 and 0.23 K. BGP-induced responses are simulated by three models in areas of intense LULCC of varying sign and magnitude (between −0.47 and 0.10 K. Modifications of the land carbon pool by LULCC are disentangled in accordance with processes that can lead to increases and decreases in this carbon pool. Global land carbon losses due to LULCC are simulated by all models: 218, 57, 35 and 34 Gt C by MPI-ESM-LR, MIROC-ESM, IPSL-CM5A-LR and CanESM2, respectively. On the contrary, the CO2-fertilization effect caused by elevated atmospheric CO2 concentrations due to LULCC leads to a land carbon gain of 39 Gt C in MPI-ESM-LR and is almost negligible in the other models. A substantial part of the spread in models' responses to LULCC is attributed to the differences in implementation of LULCC (e.g., whether pastures or crops are simulated explicitly and the simulation of specific processes. Simple idealized experiments with clear protocols for implementing LULCC in ESMs are needed to increase the understanding of model responses and the statistical significance of results, especially when analyzing the regional-scale impacts of LULCC.

Ecosystem-atmosphere exchange of carbon in a heathland under future climatic conditions

DEFF Research Database (Denmark)

Selsted, Merete Bang

understanding plant and soil responses to such changes are necessary, as ecosystems potentially can ameliorate or accelerate global change. To predict the feedback of ecosystems to the atmospheric CO2 concentrations experiments imitating global change effects are therefore an important tool. This work....... Fluxes of CO2 from soil to atmosphere depend on a physical equilibrium between those two medias, why it is important to keep the CO2 gradient between soil and atmosphere unchanged during measurement. Uptake to plants via photosynthesis depends on a physiological process, which depends strongly...... on the atmospheric CO2 concentration. Photosynthesis and respiration run in parallel during measurements of net ecosystem exchange, and these measurements should therefore be performed with care to both the atmospheric CO2 concentration and the CO2 soil-atmosphere gradient....

The Global Methane Budget 2000-2012

Science.gov (United States)

Saunois, Marielle; Bousquet, Philippe; Poulter, Benjamin; Peregon, Anna; Ciais, Philippe; Canadell, Josep G.; Dlugokencky, Edward J.; Etiope, Giuseppe; Bastviken, David; Houweling, Sander;

Impact of land use change on the land atmosphere carbon flux of South and South East Asia: A Synthesis of Dynamic Vegetation Model Results

Science.gov (United States)

Cervarich, M.; Shu, S.; Jain, A. K.; Poulter, B.; Stocker, B.; Arneth, A.; Viovy, N.; Kato, E.; Wiltshire, A.; Koven, C.; Sitch, S.; Zeng, N.; Friedlingstein, P.

2015-12-01

Understanding our present day carbon cycle and possible solutions to recent increases in atmospheric carbon dioxide is dependent upon quantifying the terrestrial carbon budget. Currently, global land cover and land use change is estimated to emit 0.9 PgC yr-1 compared to emissions due to fossil fuel combustion and cement production of 8.4 PgC yr-1. South and Southeast Asia (India, Nepal, Bhutan, Bangladesh, Burma, Thailand, Laos, Vietnam, Cambodia, Malaysia, Philippines, Indonesia, Pakistan, Myanmar, and Singapore) is a region of rapid land cover and land use change due to the continuous development of agriculture, deforestation, reforestation, afforestation, and the increased demand of land for people to live. In this study, we synthesize outputs of nine models participated in Global Carbon Budget Project to identify the carbon budget of South and southeast Asia, diagnose the contribution of land cover and land use change to carbon emissions and assess areas of uncertainty in the suite of models. Uncertainty is determined using the standard deviation and the coefficient of variation of net ecosystem exchange and its component parts. Results show the region's terrestrial biosphere was a source of carbon emissions from the 1980 to the early 1990s. During the same time period, land cover and land use change increasingly contributed to carbon emission. In the most recent two decades, the region became a carbon sink since emission due to land cover land use changes. Spatially, the greatest total emissions occurred in the tropical forest of Southeast Asia. Additionally, this is the subregion with the greatest uncertainty and greatest biomass. Model uncertainty is shown to be proportional to total biomass. The atmospheric impacts of ENSO are shown to suppress the net biosphere productivity in South and Southeast Asia leading to years of increased carbon emissions.

How China’s Options Will Determine Global Warming

Directory of Open Access Journals (Sweden)

Clifford Singer

2013-12-01

Full Text Available Carbon dioxide emissions, global average temperature, atmospheric CO2 concentrations, and surface ocean mixed layer acidity are extrapolated using analyses calibrated against extensive time series data for nine global regions. Extrapolation of historical trends without policy-driven limitations has China responsible for about half of global CO2 emissions by the middle of the twenty-first century. Results are presented for three possible actions taken by China to limit global average temperature increase to levels it considers to be to its advantage: (1 Help develop low-carbon energy technology broadly competitive with unbridled carbon emissions from burning fossil fuels; (2 Entice other countries to join in limiting use of what would otherwise be economically competitive fossil fuels; (3 Apply geo-engineering techniques such as stratospheric sulfur injection to limit global average temperature increase, without a major global reduction in carbon emissions. Taking into account China’s expected influence and approach to limiting the impact of anthropogenic climate change allows for a narrower range of possible outcomes than for a set of scenarios that are not constrained by analysis of likely policy-driven limitations. While China could hold back on implementing geoengineering given a remarkable amount of international cooperation on limiting fossil carbon burning, an outcome where geoengineering is used to delay the perceived need to limit the atmospheric CO2 concentration may be difficult to avoid.

Out of Thin Air: Microbial Utilization of Atmospheric Gaseous Organics in the Surface Ocean

KAUST Repository

Arrieta, J M; Duarte, Carlos M.; Sala, M. Montserrat; Dachs, Jordi

2016-01-01

Volatile and semi-volatile gas-phase organic carbon (GOC) is a largely neglected component of the global carbon cycle, with poorly resolved pools and fluxes of natural and anthropogenic GOC in the biosphere. Substantial amounts of atmospheric GOC are exchanged with the surface ocean, and subsequent utilization of specific GOC compounds by surface ocean microbial communities has been demonstrated. Yet, the final fate of the bulk of the atmospheric GOC entering the surface ocean is unknown. Our data show experimental evidence of efficient use of atmospheric GOC by marine prokaryotes at different locations in the NE Subtropical Atlantic, the Arctic Ocean and the Mediterranean Sea. We estimate that between 2 and 27% of the prokaryotic carbon demand was supported by GOC with a major fraction of GOC inputs being consumed within the mixed layer. The role of the atmosphere as a key vector of organic carbon subsidizing marine microbial metabolism is a novel link yet to be incorporated into the microbial ecology of the surface ocean as well as into the global carbon budget.

Out of Thin Air: Microbial Utilization of Atmospheric Gaseous Organics in the Surface Ocean.

Science.gov (United States)

Arrieta, Jesús M; Duarte, Carlos M; Sala, M Montserrat; Dachs, Jordi

2015-01-01

Volatile and semi-volatile gas-phase organic carbon (GOC) is a largely neglected component of the global carbon cycle, with poorly resolved pools and fluxes of natural and anthropogenic GOC in the biosphere. Substantial amounts of atmospheric GOC are exchanged with the surface ocean, and subsequent utilization of specific GOC compounds by surface ocean microbial communities has been demonstrated. Yet, the final fate of the bulk of the atmospheric GOC entering the surface ocean is unknown. Our data show experimental evidence of efficient use of atmospheric GOC by marine prokaryotes at different locations in the NE Subtropical Atlantic, the Arctic Ocean and the Mediterranean Sea. We estimate that between 2 and 27% of the prokaryotic carbon demand was supported by GOC with a major fraction of GOC inputs being consumed within the mixed layer. The role of the atmosphere as a key vector of organic carbon subsidizing marine microbial metabolism is a novel link yet to be incorporated into the microbial ecology of the surface ocean as well as into the global carbon budget.

Out of thin air: Microbial utilization of atmospheric gaseous organics in the surface ocean

Directory of Open Access Journals (Sweden)

Jesus M Arrieta

2016-01-01

Full Text Available Volatile and semi-volatile gas-phase organic carbon (GOC is a largely neglected component of the global carbon cycle, with poorly resolved pools and fluxes of natural and anthropogenic GOC in the biosphere. Substantial amounts of atmospheric GOC are exchanged with the surface ocean, and subsequent utilization of specific GOC compounds by surface ocean microbial communities has been demonstrated. Yet, the final fate of the bulk of the atmospheric GOC entering the surface ocean is unknown. Our data show experimental evidence of efficient use of atmospheric GOC by marine prokaryotes at different locations in the NE Subtropical Atlantic, the Arctic Ocean and the Mediterranean Sea. We estimate that between 2 to 27% of the prokaryotic carbon demand was supported by GOC with a major fraction of GOC inputs being consumed within the mixed layer. The role of the atmosphere as a key vector of organic carbon subsidising marine microbial metabolism is a novel link yet to be incorporated into the microbial ecology of the surface ocean as well as into the global carbon budget.

Out of Thin Air: Microbial Utilization of Atmospheric Gaseous Organics in the Surface Ocean

KAUST Repository

Arrieta, Jesus

2016-01-20

Volatile and semi-volatile gas-phase organic carbon (GOC) is a largely neglected component of the global carbon cycle, with poorly resolved pools and fluxes of natural and anthropogenic GOC in the biosphere. Substantial amounts of atmospheric GOC are exchanged with the surface ocean, and subsequent utilization of specific GOC compounds by surface ocean microbial communities has been demonstrated. Yet, the final fate of the bulk of the atmospheric GOC entering the surface ocean is unknown. Our data show experimental evidence of efficient use of atmospheric GOC by marine prokaryotes at different locations in the NE Subtropical Atlantic, the Arctic Ocean and the Mediterranean Sea. We estimate that between 2 and 27% of the prokaryotic carbon demand was supported by GOC with a major fraction of GOC inputs being consumed within the mixed layer. The role of the atmosphere as a key vector of organic carbon subsidizing marine microbial metabolism is a novel link yet to be incorporated into the microbial ecology of the surface ocean as well as into the global carbon budget.

ISLSCP II Globalview: Atmospheric CO2 Concentrations

Data.gov (United States)

National Aeronautics and Space Administration — The GlobalView Carbon Dioxide (CO2) data product contains synchronized and smoothed time series of atmospheric CO2 concentrations at selected sites that were created...

Source contributions to atmospheric fine carbon particle concentrations

Science.gov (United States)

Andrew Gray, H.; Cass, Glen R.

A Lagrangian particle-in-cell air quality model has been developed that facilitates the study of source contributions to atmospheric fine elemental carbon and fine primary total carbon particle concentrations. Model performance was tested using spatially and temporally resolved emissions and air quality data gathered for this purpose in the Los Angeles area for the year 1982. It was shown that black elemental carbon (EC) particle concentrations in that city were dominated by emissions from diesel engines including both on-highway and off-highway applications. Fine primary total carbon particle concentrations (TC=EC+organic carbon) resulted from the accumulation of small increments from a great variety of emission source types including both gasoline and diesel powered highway vehicles, stationary source fuel oil and gas combustion, industrial processes, paved road dust, fireplaces, cigarettes and food cooking (e.g. charbroilers). Strategies for black elemental carbon particle concentration control will of necessity need to focus on diesel engines, while controls directed at total carbon particle concentrations will have to be diversified over a great many source types.

[Regional and global estimates of carbon stocks and carbon sequestration capacity in forest ecosystems: A review].

Science.gov (United States)

Liu, Wei-wei; Wang, Xiao-ke; Lu, Fei; Ouyang, Zhi-yun

2015-09-01

As a dominant part of terrestrial ecosystems, forest ecosystem plays an important role in absorbing atmospheric CO2 and global climate change mitigation. From the aspects of zonal climate and geographical distribution, the present carbon stocks and carbon sequestration capacity of forest ecosystem were comprehensively examined based on the review of the latest literatures. The influences of land use change on forest carbon sequestration were analyzed, and factors that leading to the uncertainty of carbon sequestration assessment in forest ecosystem were also discussed. It was estimated that the current forest carbon stock was in the range of 652 to 927 Pg C and the carbon sequestration capacity was approximately 4.02 Pg C · a(-1). In terms of zonal climate, the carbon stock and carbon sequestration capacity of tropical forest were the maximum, about 471 Pg C and 1.02-1.3 Pg C · a(-1) respectively; then the carbon stock of boreal forest was about 272 Pg C, while its carbon sequestration capacity was the minimum, approximately 0.5 Pg C · a(-1); for temperate forest, the carbon stock was minimal, around 113 to 159 Pg C and its carbon sequestration capacity was 0.8 Pg C · a(-1). From the aspect of geographical distribution, the carbon stock of forest ecosystem in South America was the largest (187.7-290 Pg C), then followed by European (162.6 Pg C), North America (106.7 Pg C), Africa (98.2 Pg C) and Asia (74.5 Pg C), and Oceania (21.7 Pg C). In addition, carbon sequestration capacity of regional forest ecosystem was summed up as listed below: Tropical South America forest was the maximum (1276 Tg C · a(-1)), then were Tropical Africa (753 Tg C · a(-1)), North America (248 Tg C · a(-1)) and European (239 Tg C · a(-1)), and East Asia (98.8-136.5 Tg C · a(-1)) was minimum. To further reduce the uncertainty in the estimations of the carbon stock and carbon sequestration capacity of forest ecosystem, comprehensive application of long-term observation, inventories

Criterion 5: Maintenance of forest contributions to global carbon cycles

Science.gov (United States)

Stephen R. Shifley; Francisco X. Aguilar; Nianfu Song; Susan I. Stewart; David J. Nowak; Dale D. Gormanson; W. Keith Moser; Sherri Wormstead; Eric J. Greenfield

2012-01-01

Northern forests cover more than 42 percent of the region and are enormous reservoirs of carbon. Through photosynthesis, live trees emit oxygen in exchange for carbon dioxide they pull from the atmosphere. As a tree grows it stores carbon in wood above and below ground, and sequestered carbon comprises about half of its dry weight. Dead trees and down logs are also...

Carbon Dioxide Information Analysis Center and World Data Center for Atmospheric Trace Gases Fiscal Year 2001 Annual Report

Energy Technology Data Exchange (ETDEWEB)

Cushman, R.M.

2002-10-15

The Carbon Dioxide Information Analysis Center (CDIAC), which includes the World Data Center (WDC) for Atmospheric Trace Gases, is the primary global change data and information analysis center of the U.S. Department of Energy (DOE). More than just an archive of data sets and publications, CDIAC has, since its inception in 1982, enhanced the value of its holdings through intensive quality assurance, documentation, and integration. Whereas many traditional data centers are discipline-based (for example, meteorology or oceanography), CDIAC's scope includes potentially anything and everything that would be of value to users concerned with the greenhouse effect and global climate change, including concentrations of carbon dioxide (CO{sub 2}) and other radiatively active gases in the atmosphere; the role of the terrestrial biosphere and the oceans in the biogeochemical cycles of greenhouse gases; emissions of CO{sub 2} and other trace gases to the atmosphere; long-term climate trends; the effects of elevated CO{sub 2} on vegetation; and the vulnerability of coastal areas to rising sea levels. CDIAC is located within the Environmental Sciences Division (ESD) at Oak Ridge National Laboratory (ORNL) in Oak Ridge, Tennessee. CDIAC is co-located with ESD researchers investigating global-change topics, such as the global carbon cycle and the effects of carbon dioxide on climate and vegetation. CDIAC staff are also connected with current ORNL research on related topics, such as renewable energy and supercomputing technologies. CDIAC is supported by the Environmental Sciences Division (Jerry Elwood, Director) of DOE's Office of Biological and Environmental Research. CDIAC represents DOE in the multi-agency Global Change Data and Information System (GCDIS). Wanda Ferrell is DOE's Program Manager with overall responsibility for CDIAC. Roger Dahlman is responsible for CDIAC's AmeriFlux tasks, and Anna Palmisano for CDIAC's Ocean Data tasks. CDIAC is made

Uptake by the Atlantic Ocean of excess atmospheric carbon dioxide and radiocarbon

International Nuclear Information System (INIS)

Bolin, B.; Bjorkstrom, A.

1989-01-01

Inverse methods have been used to deduce water circulation, spatial patterns of turbulent exchange and biological activity in the Atlantic Ocean, by using a set of stationary tracers and a condition of quasi-geostrophic flow. The solution yields a direct meridional circulation cell with descending motion in the northern Atlantic with an intensity of 20-25 Sverdrup, a reasonable distribution of vertical turbulent transfer in the uppermost ocean layers and comparatively large rates of detritus formation, about 4.5 Pg C yr -1 . The solution is used to compute the invasion of tritium 1955-1983, and the uptake of excess radiocarbon and carbon dioxide during the period 1760-1983. A fair agreement between computed and observed changes of tritium and 14 C is obtained, but the period of observations is too short to serve as a conclusive test model. The uptake of carbon dioxide during the 220 years period into the Atlantic Ocean is 33 ± 5 Pg and it is further found that significant variations of the uptake fraction of the CO 2 emissions may have occurred due to varying rates of emissions in gorce of time. The conclusion is drawn that the ocean and its carbonate system may not have been the only sink for anthropogenic emissions of carbon dioxide into the atmosphere. Means for how to further improve the model and its capability to reproduce the ocean behaviour are discussed. Burning of fossil fuels, deforestation and changing land use have changed the global carbon cycle very significant during the last two centuries

The Global Turnover Time Distribution of Soil Carbon Derived from a Meta-analysis of Radiocarbon Profiles

Science.gov (United States)

He, Y.; Randerson, J. T.; Allison, S. D.; Torn, M. S.; Harden, J. W.; Smith, L. J.; van der Voort, T.; Trumbore, S.

2015-12-01

Soil is the largest terrestrial carbon reservoir and may influence the sign and magnitude of carbon cycle feedbacks under climate change. Soil carbon turnover times provide information about the sensitivity of carbon pools to changes in inputs and warming. The spatial and vertical distribution of soil carbon turnover times emerges from the interplay between climate, vegetation, and soil properties. Radiocarbon levels of soil organic matter can be used to estimate soil carbon turnover using models that take into account radioactive decay over centuries to millennia and inputs of 14C from atmospheric weapons testing ("bomb carbon") during the second half of the 20th century. By synthesizing more than 200 soil radiocarbon profiles from all major biomes and soil orders, we 1) explored the major controlling factors for soil carbon turnover times of surface and deeper soil layers; 2) developed predictive models (tree-based regression, support vector regression and linear regression models) of Δ14C that depends on depth, climate, vegetation, and soil types; and 3) extrapolated the predictive model to produce the first global distribution of soil carbon turnover times to the depth of 1m. Preliminary results indicated that climate and depth were primary controls of the vertical distribution of Δ14C, contributing to about 70% of the variability in our model. Vegetation and soil order exerted similar level of controls (about 15% each). The predictive model performed reasonably well with an R2 of 0.81 and RMSE (root-mean-squared error) of about 50‰ for topsoil and 100‰ for subsoil, as estimated using cross-validation. Extrapolation of the predictive model to the globe in combination with existing soil carbon information (e.g., Harmonized World Soil Database) indicated that more than half of the global total soil carbon in the top 1m had a turnover time of less than 500 years. Subsoils (30-100cm) had millennium-scale turnover times, with the majority (70%) turning over

Removal of Atmospheric Ethanol by Wet Deposition: A Global Flux Estimate

Science.gov (United States)

Felix, J. D. D.; Willey, J. D.; Avery, B.; Thomas, R.; Mullaugh, K.; Kieber, R. J.; Mead, R. N.; Helms, J. R.; Campos, L.; Shimizu, M. S.; Guibbina, F.

2017-12-01

Global ethanol fuel consumption has increased exponentially over the last two decades and the US plans to double annual renewable fuel production in the next five years as required by the renewable fuel standard. Regardless of the technology or feedstock used to produce the renewable fuel, the primary end product will be ethanol. Increasing ethanol fuel consumption will have an impact on the oxidizing capacity of the atmosphere and increase atmospheric concentrations of the secondary pollutant peroxyacetyl nitrate as well a variety of VOCs with relatively high ozone reactivities (e.g. ethanol, formaldehyde, acetaldehyde). Despite these documented effects of ethanol emissions on atmospheric chemistry, current global atmospheric ethanol budget models have large uncertainties in the magnitude of ethanol sources and sinks. The presented work investigates the global wet deposition sink by providing the first estimate of the global wet deposition flux of ethanol (2.4 ± 1.6 Tg/yr) based on empirical wet deposition data (219 samples collected at 12 locations). This suggests the wet deposition sink removes between 6 and 17% of atmospheric ethanol annually. Concentrations of ethanol in marine wet deposition (25 ± 6 nM) were an order of magnitude less than in the majority of terrestrial deposition (345 ± 280 nM). Terrestrial deposition collected in locations impacted by high local sources of biofuel usage and locations downwind from ethanol distilleries were an order of magnitude higher in ethanol concentration (3090 ± 448 nM) compared to deposition collected in terrestrial locations not impacted by these sources. These results indicate that wet deposition of ethanol is heavily influenced by local sources and ethanol emission impacts on air quality may be more significant in highly populated areas. As established and developing countries continue to rapidly increase ethanol fuel consumption and subsequent emissions, understanding the magnitude of all ethanol sources and

Marine atmospheric corrosion of carbon steels

Directory of Open Access Journals (Sweden)

Morcillo, Manuel

2015-06-01

Full Text Available Basic research on marine atmospheric corrosion of carbon steels is a relatively young scientific field and there continue to be great gaps in this area of knowledge. The presence of akaganeite in the corrosion products that form on steel when it is exposed to marine atmospheres leads to a notable increase in the corrosion rate. This work addresses the following issues: (a environmental conditions necessary for akaganeite formation; (b characterisation of akaganeite in the corrosion products formed; (c corrosion mechanisms of carbon steel in marine atmospheres; (d exfoliation of rust layers formed in highly aggressive marine atmospheres; (e long-term corrosion rate prediction; and (f behaviour of weathering steels. Field research has been carried out at Cabo Vilano wind farm (Camariñas, Galicia in a wide range of atmospheric salinities and laboratory work involving the use of conventional atmospheric corrosion techniques and near-surface and bulk sensitive analytical techniques: scanning electron microscopy (SEM/energy dispersive spectrometry (EDS, X-ray diffraction (XRD, Mössbauer spectroscopy and SEM/μRaman spectroscopy.La investigación fundamental en corrosión atmosférica marina de aceros al carbono es un campo científico relativamente joven que presenta grandes lagunas de conocimiento. La formación de akaganeíta en los productos de corrosión que se forman sobre el acero cuando se expone a atmósferas marinas conduce a un incremento notable de la velocidad de corrosión. En el trabajo se abordan las siguientes cuestiones: (a condiciones ambientales necesarias para la formación de akaganeíta, (b caracterización de la akaganeíta en los productos de corrosión formados, (c mecanismos de corrosión del acero al carbono en atmósferas marinas, (d exfoliación de las capas de herrumbre formadas en atmósferas marinas muy agresivas, (e predicción de la velocidad de corrosión a largo plazo, y (f comportamiento de aceros patinables. La

Global atmospheric chemistry – which air matters

Directory of Open Access Journals (Sweden)

M. J. Prather

2017-07-01

Full Text Available An approach for analysis and modeling of global atmospheric chemistry is developed for application to measurements that provide a tropospheric climatology of those heterogeneously distributed, reactive species that control the loss of methane and the production and loss of ozone. We identify key species (e.g., O3, NOx, HNO3, HNO4, C2H3NO5, H2O, HOOH, CH3OOH, HCHO, CO, CH4, C2H6, acetaldehyde, acetone and presume that they can be measured simultaneously in air parcels on the scale of a few km horizontally and a few tenths of a km vertically. As a first step, six global models have prepared such climatologies sampled at the modeled resolution for August with emphasis on the vast central Pacific Ocean basin. Objectives of this paper are to identify and characterize differences in model-generated reactivities as well as species covariances that could readily be discriminated with an unbiased climatology. A primary tool is comparison of multidimensional probability densities of key species weighted by the mass of such parcels or frequency of occurrence as well as by the reactivity of the parcels with respect to methane and ozone. The reactivity-weighted probabilities tell us which parcels matter in this case, and this method shows skill in differentiating among the models' chemistry. Testing 100 km scale models with 2 km measurements using these tools also addresses a core question about model resolution and whether fine-scale atmospheric structures matter to the overall ozone and methane budget. A new method enabling these six global chemistry–climate models to ingest an externally sourced climatology and then compute air parcel reactivity is demonstrated. Such an objective climatology containing these key species is anticipated from the NASA Atmospheric Tomography (ATom aircraft mission (2015–2020, executing profiles over the Pacific and Atlantic Ocean basins. This modeling study addresses a core part of the design of ATom.