Sample records for carbon cycle components
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[Modeling of carbon cycling in terrestrial ecosystem: a review].
Mao, Liuxi; Sun, Yanling; Yan, Xiaodong
2006-11-01
Terrestrial carbon cycling is one of the important issues in global change research, while carbon cycling modeling has become a necessary method and tool in understanding this cycling. This paper reviewed the research progress in terrestrial carbon cycling, with the focus on the basic framework of simulation modeling, two essential models of carbon cycling, and the classes of terrestrial carbon cycling modeling, and analyzed the present situation of terrestrial carbon cycling modeling. It was pointed out that the future research direction could be based on the biophysical modeling of dynamic vegetation, and this modeling could be an important component in the earth system modeling.
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Matrix approach to uncertainty assessment and reduction for modeling terrestrial carbon cycle
NASA Astrophysics Data System (ADS)
Luo, Y.; Xia, J.; Ahlström, A.; Zhou, S.; Huang, Y.; Shi, Z.; Wang, Y.; Du, Z.; Lu, X.
2017-12-01
Terrestrial ecosystems absorb approximately 30% of the anthropogenic carbon dioxide emissions. This estimate has been deduced indirectly: combining analyses of atmospheric carbon dioxide concentrations with ocean observations to infer the net terrestrial carbon flux. In contrast, when knowledge about the terrestrial carbon cycle is integrated into different terrestrial carbon models they make widely different predictions. To improve the terrestrial carbon models, we have recently developed a matrix approach to uncertainty assessment and reduction. Specifically, the terrestrial carbon cycle has been commonly represented by a series of carbon balance equations to track carbon influxes into and effluxes out of individual pools in earth system models. This representation matches our understanding of carbon cycle processes well and can be reorganized into one matrix equation without changing any modeled carbon cycle processes and mechanisms. We have developed matrix equations of several global land C cycle models, including CLM3.5, 4.0 and 4.5, CABLE, LPJ-GUESS, and ORCHIDEE. Indeed, the matrix equation is generic and can be applied to other land carbon models. This matrix approach offers a suite of new diagnostic tools, such as the 3-dimensional (3-D) parameter space, traceability analysis, and variance decomposition, for uncertainty analysis. For example, predictions of carbon dynamics with complex land models can be placed in a 3-D parameter space (carbon input, residence time, and storage potential) as a common metric to measure how much model predictions are different. The latter can be traced to its source components by decomposing model predictions to a hierarchy of traceable components. Then, variance decomposition can help attribute the spread in predictions among multiple models to precisely identify sources of uncertainty. The highly uncertain components can be constrained by data as the matrix equation makes data assimilation computationally possible. We will illustrate various applications of this matrix approach to uncertainty assessment and reduction for terrestrial carbon cycle models.
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Society and the Carbon Cycle: A Social Science Perspective
NASA Astrophysics Data System (ADS)
Romero-Lankao, P.
2017-12-01
Societal activities, actions, and practices affect the carbon cycle and the climate of North America in complex ways. Carbon is a key component for the functioning of croplands, grasslands, forests. Carbon fuels our industry, transportation (vehicles and roadways), buildings, and other structures. Drawing on results from the SOCCR-2, this presentation uses a social science perspective to address three scientific questions. How do human actions and activities affect the carbon cycle? How human systems such as cities, agricultural field and forests are affected by changes in the carbon cycle? How is carbon management enabled and constraint by socio-political dynamics?
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Nitrogen attenuation of terrestrial carbon cycle response to global environmental factors
Atul Jain; Xiaojuan Yang; Haroon Kheshgi; A. David McGuire; Wilfred Post; David Kicklighter
2009-01-01
Nitrogen cycle dynamics have the capacity to attenuate the magnitude of global terrestrial carbon sinks and sources driven by CO2 fertilization and changes in climate. In this study, two versions of the terrestrial carbon and nitrogen cycle components of the Integrated Science Assessment Model (ISAM) are used to evaluate how variation in nitrogen...
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Carbon allocation in forest ecosystems
Creighton M. Litton; James W. Raich; Michael G. Ryan
2007-01-01
Carbon allocation plays a critical role in forest ecosystem carbon cycling. We reviewed existing literature and compiled annual carbon budgets for forest ecosystems to test a series of hypotheses addressing the patterns, plasticity, and limits of three components of allocation: biomass, the amount of material present; flux, the flow of carbon to a component per unit...
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SNTP propellant management system
NASA Technical Reports Server (NTRS)
Tippetts, Tom
1993-01-01
Viewgraphs on the following are presented: (1) space nuclear thermal propulsion (SNTP) propellant management system; (2) SNTP cycle selection; (3) NTP system components unique design constraints; (4) bleed cycle unique design requirement for turbopump; (5) bleed cycle turbopump; (6) SNTP carbon-carbon turbine wheel; and (7) turbine development program.
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Climate extremes and the carbon cycle.
Reichstein, Markus; Bahn, Michael; Ciais, Philippe; Frank, Dorothea; Mahecha, Miguel D; Seneviratne, Sonia I; Zscheischler, Jakob; Beer, Christian; Buchmann, Nina; Frank, David C; Papale, Dario; Rammig, Anja; Smith, Pete; Thonicke, Kirsten; van der Velde, Marijn; Vicca, Sara; Walz, Ariane; Wattenbach, Martin
2013-08-15
The terrestrial biosphere is a key component of the global carbon cycle and its carbon balance is strongly influenced by climate. Continuing environmental changes are thought to increase global terrestrial carbon uptake. But evidence is mounting that climate extremes such as droughts or storms can lead to a decrease in regional ecosystem carbon stocks and therefore have the potential to negate an expected increase in terrestrial carbon uptake. Here we explore the mechanisms and impacts of climate extremes on the terrestrial carbon cycle, and propose a pathway to improve our understanding of present and future impacts of climate extremes on the terrestrial carbon budget.
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LOSCAR: Long-term Ocean-atmosphere-Sediment CArbon cycle Reservoir Model
NASA Astrophysics Data System (ADS)
Zeebe, R. E.
2011-06-01
The LOSCAR model is designed to efficiently compute the partitioning of carbon between ocean, atmosphere, and sediments on time scales ranging from centuries to millions of years. While a variety of computationally inexpensive carbon cycle models are already available, many are missing a critical sediment component, which is indispensable for long-term integrations. One of LOSCAR's strengths is the coupling of ocean-atmosphere routines to a computationally efficient sediment module. This allows, for instance, adequate computation of CaCO3 dissolution, calcite compensation, and long-term carbon cycle fluxes, including weathering of carbonate and silicate rocks. The ocean component includes various biogeochemical tracers such as total carbon, alkalinity, phosphate, oxygen, and stable carbon isotopes. We have previously published applications of the model tackling future projections of ocean chemistry and weathering, pCO2 sensitivity to carbon cycle perturbations throughout the Cenozoic, and carbon/calcium cycling during the Paleocene-Eocene Thermal Maximum. The focus of the present contribution is the detailed description of the model including numerical architecture, processes and parameterizations, tuning, and examples of input and output. Typical CPU integration times of LOSCAR are of order seconds for several thousand model years on current standard desktop machines. The LOSCAR source code in C can be obtained from the author by sending a request to loscar.model@gmail.com.
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Environmental Aspects of Use of Recycled Carbon Fiber Composites in Automotive Applications.
Meng, Fanran; McKechnie, Jon; Turner, Thomas; Wong, Kok H; Pickering, Stephen J
2017-11-07
The high cost and energy intensity of virgin carbon fiber manufacture provides an opportunity to recover substantial value from carbon fiber reinforced plastic wastes. In this study, we assess the life cycle environmental implications of recovering carbon fiber and producing composite materials as substitutes for conventional and proposed lightweight materials in automotive applications (e.g., steel, aluminum, virgin carbon fiber). Key parameters for the recycled carbon fiber materials, including fiber volume fraction and fiber alignment, are investigated to identify beneficial uses of recycled carbon fiber in the automotive sector. Recycled carbon fiber components can achieve the lowest life cycle environmental impacts of all materials considered, although the actual impact is highly dependent on the design criteria (λ value) of the specific component. Low production impacts associated with recycled carbon fiber components are observed relative to lightweight competitor materials (e.g., aluminum, virgin carbon fiber reinforced plastic). In addition, recycled carbon fiber components have low in-use energy use due to mass reductions and associated reduction in mass-induced fuel consumption. The results demonstrate environmental feasibility of the CFRP recycling materials, supporting the emerging commercialization of CF recycling technologies and identifying significant potential market opportunities in the automotive sector.
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Carbon Storage in Urban Areas in the USA
NASA Astrophysics Data System (ADS)
Churkina, G.; Brown, D.; Keoleian, G.
2007-12-01
It is widely accepted that human settlements occupy a small proportion of the landmass and therefore play a relatively small role in the dynamics of the global carbon cycle. Most modeling studies focusing on the land carbon cycle use models of varying complexity to estimate carbon fluxes through forests, grasses, and croplands, but completely omit urban areas from their scope. Here, we estimate carbon storage in urban areas within the United States, defined to encompass a range of observed settlement densities, and its changes from 1950 to 2000. We show that this storage is not negligible and has been continuously increasing. We include natural- and human-related components of urban areas in our estimates. The natural component includes carbon storage in urban soil and vegetation. The human related component encompasses carbon stored long term in buildings, furniture, cars, and waste. The study suggests that urban areas should receive continued attention in efforts to accurately account for carbon uptake and storage in terrestrial systems.
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One of the major uncertainties concerning the role of tropical forests in the global carbon cycle is the lack of adequate data on the carbon content of all their components. The goal of this study was to contribute to filling this data gap by estimating the quantity of carbon in ...
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Claire M. Ruffing; Kathleen A. Dwire; Melinda D. Daniels
2016-01-01
Streams and their accompanying riparian environments are intrinsic components of terrestrial carbon cycling. However, they have been understudied in terms of the magnitude of their storage components and the role of disturbance in determining carbon storage capacity. This study presents partial carbon budgets for stream-riparian corridors along six study...
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NASA Astrophysics Data System (ADS)
Leung, L. R.; Thornton, P. E.; Riley, W. J.; Calvin, K. V.
2017-12-01
Towards the goal of understanding the contributions from natural and managed systems to current and future greenhouse gas fluxes and carbon-climate and carbon-CO2 feedbacks, efforts have been underway to improve representations of the terrestrial, river, and human components of the ACME earth system model. Broadly, our efforts include implementation and comparison of approaches to represent the nutrient cycles and nutrient limitations on ecosystem production, extending the river transport model to represent sediment and riverine biogeochemistry, and coupling of human systems such as irrigation, reservoir operations, and energy and land use with the ACME land and river components. Numerical experiments have been designed to understand how terrestrial carbon, nitrogen, and phosphorus cycles regulate climate system feedbacks and the sensitivity of the feedbacks to different model treatments, examine key processes governing sediment and biogeochemistry in the rivers and their role in the carbon cycle, and exploring the impacts of human systems in perturbing the hydrological and carbon cycles and their interactions. This presentation will briefly introduce the ACME modeling approaches and discuss preliminary results and insights from numerical experiments that lay the foundation for improving understanding of the integrated climate-biogeochemistry-human system.
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LOSCAR: Long-term Ocean-atmosphere-Sediment CArbon cycle Reservoir Model v2.0.4
NASA Astrophysics Data System (ADS)
Zeebe, R. E.
2012-01-01
The LOSCAR model is designed to efficiently compute the partitioning of carbon between ocean, atmosphere, and sediments on time scales ranging from centuries to millions of years. While a variety of computationally inexpensive carbon cycle models are already available, many are missing a critical sediment component, which is indispensable for long-term integrations. One of LOSCAR's strengths is the coupling of ocean-atmosphere routines to a computationally efficient sediment module. This allows, for instance, adequate computation of CaCO3 dissolution, calcite compensation, and long-term carbon cycle fluxes, including weathering of carbonate and silicate rocks. The ocean component includes various biogeochemical tracers such as total carbon, alkalinity, phosphate, oxygen, and stable carbon isotopes. LOSCAR's configuration of ocean geometry is flexible and allows for easy switching between modern and paleo-versions. We have previously published applications of the model tackling future projections of ocean chemistry and weathering, pCO2 sensitivity to carbon cycle perturbations throughout the Cenozoic, and carbon/calcium cycling during the Paleocene-Eocene Thermal Maximum. The focus of the present contribution is the detailed description of the model including numerical architecture, processes and parameterizations, tuning, and examples of input and output. Typical CPU integration times of LOSCAR are of order seconds for several thousand model years on current standard desktop machines. The LOSCAR source code in C can be obtained from the author by sending a request to loscar.model@gmail.com.
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Compiled records of carbon isotopes in atmospheric CO2 for historical simulations in CMIP6
NASA Astrophysics Data System (ADS)
Graven, Heather; Allison, Colin E.; Etheridge, David M.; Hammer, Samuel; Keeling, Ralph F.; Levin, Ingeborg; Meijer, Harro A. J.; Rubino, Mauro; Tans, Pieter P.; Trudinger, Cathy M.; Vaughn, Bruce H.; White, James W. C.
2017-12-01
The isotopic composition of carbon (Δ14C and δ13C) in atmospheric CO2 and in oceanic and terrestrial carbon reservoirs is influenced by anthropogenic emissions and by natural carbon exchanges, which can respond to and drive changes in climate. Simulations of 14C and 13C in the ocean and terrestrial components of Earth system models (ESMs) present opportunities for model evaluation and for investigation of carbon cycling, including anthropogenic CO2 emissions and uptake. The use of carbon isotopes in novel evaluation of the ESMs' component ocean and terrestrial biosphere models and in new analyses of historical changes may improve predictions of future changes in the carbon cycle and climate system. We compile existing data to produce records of Δ14C and δ13C in atmospheric CO2 for the historical period 1850-2015. The primary motivation for this compilation is to provide the atmospheric boundary condition for historical simulations in the Coupled Model Intercomparison Project 6 (CMIP6) for models simulating carbon isotopes in the ocean or terrestrial biosphere. The data may also be useful for other carbon cycle modelling activities.
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NASA Astrophysics Data System (ADS)
Strassmann, Kuno M.; Joos, Fortunat
2018-05-01
The Bern Simple Climate Model (BernSCM) is a free open-source re-implementation of a reduced-form carbon cycle-climate model which has been used widely in previous scientific work and IPCC assessments. BernSCM represents the carbon cycle and climate system with a small set of equations for the heat and carbon budget, the parametrization of major nonlinearities, and the substitution of complex component systems with impulse response functions (IRFs). The IRF approach allows cost-efficient yet accurate substitution of detailed parent models of climate system components with near-linear behavior. Illustrative simulations of scenarios from previous multimodel studies show that BernSCM is broadly representative of the range of the climate-carbon cycle response simulated by more complex and detailed models. Model code (in Fortran) was written from scratch with transparency and extensibility in mind, and is provided open source. BernSCM makes scientifically sound carbon cycle-climate modeling available for many applications. Supporting up to decadal time steps with high accuracy, it is suitable for studies with high computational load and for coupling with integrated assessment models (IAMs), for example. Further applications include climate risk assessment in a business, public, or educational context and the estimation of CO2 and climate benefits of emission mitigation options.
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NASA Astrophysics Data System (ADS)
Galbraith, D.; Levine, N. M.; Christoffersen, B. O.; Imbuzeiro, H. A.; Powell, T.; Costa, M. H.; Saleska, S. R.; Moorcroft, P. R.; Malhi, Y.
2014-12-01
The mathematical codes embedded within different vegetation models ultimately represent alternative hypotheses of biosphere functioning. While formulations for some processes (e.g. leaf-level photosynthesis) are often shared across vegetation models, other processes (e.g. carbon allocation) are much more variable in their representation across models. This creates the opportunity for equifinality - models can simulate similar values of key metrics such as NPP or biomass through very different underlying causal pathways. Intensive carbon cycle measurements allow for quantification of a comprehensive suite of carbon fluxes such as the productivity and respiration of leaves, roots and wood, allowing for in-depth assessment of carbon flows within ecosystems. Thus, they provide important information on poorly-constrained C-cycle processes such as allocation. We conducted an in-depth evaluation of the ability of four commonly used dynamic global vegetation models (CLM, ED2, IBIS, JULES) to simulate carbon cycle processes at ten lowland Amazonian rainforest sites where individual C-cycle components have been measured. The rigorous model-data comparison procedure allowed identification of biases which were specific to different models, providing clear avenues for model improvement and allowing determination of internal C-cycling pathways that were better supported by data. Furthermore, the intensive C-cycle data allowed for explicit testing of the validity of a number of assumptions made by specific models in the simulation of carbon allocation and plant respiration. For example, the ED2 model assumes that maintenance respiration of stems is negligible while JULES assumes equivalent allocation of NPP to fine roots and leaves. We argue that field studies focusing on simultaneous measurement of a large number of component fluxes are fundamentally important for reducing uncertainty in vegetation model simulations.
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pyhector: A Python interface for the simple climate model Hector
Willner, Sven N.; Hartin, Corinne; Gieseke, Robert
2017-04-01
Here, pyhector is a Python interface for the simple climate model Hector (Hartin et al. 2015) developed in C++. Simple climate models like Hector can, for instance, be used in the analysis of scenarios within integrated assessment models like GCAM1, in the emulation of complex climate models, and in uncertainty analyses. Hector is an open-source, object oriented, simple global climate carbon cycle model. Its carbon cycle consists of a one pool atmosphere, three terrestrial pools which can be broken down into finer biomes or regions, and four carbon pools in the ocean component. The terrestrial carbon cycle includes primary productionmore » and respiration fluxes. The ocean carbon cycle circulates carbon via a simplified thermohaline circulation, calculating air-sea fluxes as well as the marine carbonate system. The model input is time series of greenhouse gas emissions; as example scenarios for these the Pyhector package contains the Representative Concentration Pathways (RCPs)2.« less
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DOE Office of Scientific and Technical Information (OSTI.GOV)
Willner, Sven N.; Hartin, Corinne; Gieseke, Robert
Here, pyhector is a Python interface for the simple climate model Hector (Hartin et al. 2015) developed in C++. Simple climate models like Hector can, for instance, be used in the analysis of scenarios within integrated assessment models like GCAM1, in the emulation of complex climate models, and in uncertainty analyses. Hector is an open-source, object oriented, simple global climate carbon cycle model. Its carbon cycle consists of a one pool atmosphere, three terrestrial pools which can be broken down into finer biomes or regions, and four carbon pools in the ocean component. The terrestrial carbon cycle includes primary productionmore » and respiration fluxes. The ocean carbon cycle circulates carbon via a simplified thermohaline circulation, calculating air-sea fluxes as well as the marine carbonate system. The model input is time series of greenhouse gas emissions; as example scenarios for these the Pyhector package contains the Representative Concentration Pathways (RCPs)2.« less
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Engine Cycle Analysis for a Particle Bed Reactor Nuclear Rocket
1991-03-01
0 DTIC USERS UNCLASSIFIED 22a. NAME OF RESPONSIBLE INDIVIDUAL ZZb. TELEPHONE (Include Area Code) 22c. OFFICE SYMBOL Lt Timothy J . Lawrence 805-275...Cycle with 2000 MW PBR and Uncooled Nozzle J : Output for Bleed Cycle with 2000 MW PBR and Cooled Nozzle K: Output for Expander Cycle with 2000 MW PBR L...Mars with carbon dioxide, the primary component of the Martian atmosphere. Carbon dioxide would delivera smaller ! j , but its use would eliminate the
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Modeling Dissolved Organic Carbon (DOC) Dynamics in Flooded Wetlands
Wetlands play an important role in the global carbon cycle and are recognized for their considerable potential to sequester carbon. Wetlands contain the largest component (18-30%) of the terrestrial carbon pool and are responsible for about a quarter of the global methane emissi...
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NASA Technical Reports Server (NTRS)
Jones, Jack A.
2004-01-01
The term champagne heat pump denotes a developmental heat pump that exploits a cycle of absorption and desorption of carbon dioxide in an alcohol or other organic liquid. Whereas most heat pumps in common use in the United States are energized by mechanical compression, the champagne heat pump is energized by heating. The concept of heat pumps based on other absorption cycles energized by heat has been understood for years, but some of these heat pumps are outlawed in many areas because of the potential hazards posed by leakage of working fluids. For example, in the case of the water/ammonia cycle, there are potential hazards of toxicity and flammability. The organic-liquid/carbon dioxide absorption/desorption cycle of the champagne heat pump is similar to the water/ammonia cycle, but carbon dioxide is nontoxic and environmentally benign, and one can choose an alcohol or other organic liquid that is also relatively nontoxic and environmentally benign. Two candidate nonalcohol organic liquids are isobutyl acetate and amyl acetate. Although alcohols and many other organic liquids are flammable, they present little or no flammability hazard in the champagne heat pump because only the nonflammable carbon dioxide component of the refrigerant mixture is circulated to the evaporator and condenser heat exchangers, which are the only components of the heat pump in direct contact with air in habitable spaces.
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NASA Astrophysics Data System (ADS)
Scholze, Marko; Buchwitz, Michael; Dorigo, Wouter; Guanter, Luis; Quegan, Shaun
2017-07-01
The global carbon cycle is an important component of the Earth system and it interacts with the hydrology, energy and nutrient cycles as well as ecosystem dynamics. A better understanding of the global carbon cycle is required for improved projections of climate change including corresponding changes in water and food resources and for the verification of measures to reduce anthropogenic greenhouse gas emissions. An improved understanding of the carbon cycle can be achieved by data assimilation systems, which integrate observations relevant to the carbon cycle into coupled carbon, water, energy and nutrient models. Hence, the ingredients for such systems are a carbon cycle model, an algorithm for the assimilation and systematic and well error-characterised observations relevant to the carbon cycle. Relevant observations for assimilation include various in situ measurements in the atmosphere (e.g. concentrations of CO2 and other gases) and on land (e.g. fluxes of carbon water and energy, carbon stocks) as well as remote sensing observations (e.g. atmospheric composition, vegetation and surface properties).We briefly review the different existing data assimilation techniques and contrast them to model benchmarking and evaluation efforts (which also rely on observations). A common requirement for all assimilation techniques is a full description of the observational data properties. Uncertainty estimates of the observations are as important as the observations themselves because they similarly determine the outcome of such assimilation systems. Hence, this article reviews the requirements of data assimilation systems on observations and provides a non-exhaustive overview of current observations and their uncertainties for use in terrestrial carbon cycle data assimilation. We report on progress since the review of model-data synthesis in terrestrial carbon observations by Raupach et al.(2005), emphasising the rapid advance in relevant space-based observations.
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Decadally cycling soil carbon is more sensitive to warming than faster-cycling soil carbon.
Lin, Junjie; Zhu, Biao; Cheng, Weixin
2015-12-01
The response of soil organic carbon (SOC) pools to globally rising surface temperature crucially determines the feedback between climate change and the global carbon cycle. However, there is a lack of studies investigating the temperature sensitivity of decomposition for decadally cycling SOC which is the main component of total soil carbon stock and the most relevant to global change. We tackled this issue using two decadally (13) C-labeled soils and a much improved measuring system in a long-term incubation experiment. Results indicated that the temperature sensitivity of decomposition for decadally cycling SOC (>23 years in one soil and >55 years in the other soil) was significantly greater than that for faster-cycling SOC (<23 or 55 years) or for the entire SOC stock. Moreover, decadally cycling SOC contributed substantially (35-59%) to the total CO2 loss during the 360-day incubation. Overall, these results indicate that the decomposition of decadally cycling SOC is highly sensitive to temperature change, which will likely make this large SOC stock vulnerable to loss by global warming in the 21st century and beyond. © 2015 John Wiley & Sons Ltd.
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Hydrology and landscape structure control subalpine catchment carbon export
Vincent Jerald Pacific
2009-01-01
Carbon export from high elevation ecosystems is a critical component of the global carbon cycle. Ecosystems in northern latitudes have become the focus of much research due to their potential as large sinks of carbon in the atmosphere. However, there exists limited understanding of the controls of carbon export from complex mountain catchments due to strong spatial and...
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Variation in the carbon cycle of the Sevastopol Bay (Black Sea)
NASA Astrophysics Data System (ADS)
Orekhova, N. A.; Konovalov, S. K.
2018-01-01
Continuous increase in CO2 inventory in the ocean results in dramatic changes in marine biogeochemistry, e.g. acidification. That is why temporal and spatial variabilities in atmospheric pCO2 and dissolved inorganic carbon, including CO2, pH and alkalinity in water, as well as organic and inorganic carbon in bottom sediments have to be studied together making possible to resolve the key features of the carbon cycle transformation. A 30% increase of pCO2 in the Sevastopol Bay for 2008 - 2016 evidences changes in the DIC components ratios and a significant decrease in the ability to absorb atmospheric CO2 by surface waters. High organic carbon content in the bottom sediments and predominance of organic carbon production in the biological pump at inner parts of the bay reveal ongoing transformation of the carbon cycle. This has negative consequences for recreation, social and economic potentials of the Sevastopol region.
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Dean, W.
2002-01-01
Most of the sediment components that have accumulated in Elk Lake, Clearwater County, northwestern Minnesota, over the past 1500 years are authigenic or biogenic (CaCO3, biogenic SiO2, organic matter, iron and manganese oxyhydroxides, and iron phosphate) and are delivered to the sediment-water interface on a seasonal schedule where they are preserved as distinct annual laminae (varves). The annual biogeochemical cycles of these components are causally linked through the 'carbon pump', and are recapitulated in longer-term cycles, most prominently with a periodicity of about 400 years. Organic carbon is fixed in the epilimnion by photosynthetic removal of CO2, which also increases the pH, triggering the precipitation of CaCO3. The respiration and degradation of fixed organic carbon in the hypolimnion consumes dissolved oxygen, produces CO2, and lowers the pH so that the hypolimnion becomes anoxic and undersaturated with respect to CaCO3 during the summer. Some of the CaCO3 produced in the epilimnion is dissolved in the anoxic, lower pH hypolimnion and sediments. The amount of CaCO3 that is ultimately incorporated into the sediments is a function of how much is produced in the epilimnion and how much is consumed in the hypolimnion and the sediments. Iron, manganese, and phosphate accumulate in the anoxic hypolimnion throughout the summer. Sediment-trap studies show that at fall overturn, when iron-, manganese-, and phosphate-rich bottom waters mix with carbonate- and oxygen-rich surface waters, precipitation of iron and manganese oxyhydroxides, iron phosphate, and manganese carbonate begins and continues into the winter months. Detrital clastic material in the sediments of Elk Lake deposited over the last 1500 years is a minor component (<10% by weight) that is mostly wind-borne (eolian). Detailed analyses of the last 1500 years of the Elk Lake sediment record show distinct cycles in eolian clastic variables (e.g. aluminum, sodium, potassium, titanium, and quartz), with a periodicity of about 400 years. The 400-yr cycle in eolian clastic material does not correspond to the 400-yr cycles in redox-sensitive authigenic components, suggesting that the clastic component is responding to external forcing (wind) whereas the authigenic components are responding to internal forcing (productivity), although both may ultimately be forced by climate change. Variations in the oxygen and carbon isotopic composition of CaCO3 are small but appear to reflect small variations in ground water influx that are also driven by external forcing.
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The role of carbon dust emission as a global source of atmospheric CO2
USDA-ARS?s Scientific Manuscript database
Soil erosion redistributes soil organic carbon (SOC) within terrestrial ecosystems, to the atmosphere and oceans. Dust export is an essential component of the carbon (C) and carbon dioxide (CO2) budget, because wind erosion contributes to the C cycle by selectively removing4 SOC from vast areas and ...
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Soil organic carbon dust emission: an omitted global source of atmospheric CO2?
USDA-ARS?s Scientific Manuscript database
Soil erosion redistributes soil organic carbon (SOC) within terrestrial ecosystems, to the atmosphere and oceans. Dust export is an essential component of the carbon (C) and carbon dioxide (CO2) budget because wind erosion contributes to the C cycle by removing selectively SOC from vast areas and tr...
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NASA/GSFC Research Activities for the Global Ocean Carbon Cycle: A Prospectus for the 21st Century
NASA Technical Reports Server (NTRS)
Gregg, W. W.; Behrenfield, M. J.; Hoge, F. E.; Esaias, W. E.; Huang, N. E.; Long, S. R.; McClain, C. R.
2000-01-01
There are increasing concerns that anthropogenic inputs of carbon dioxide into the Earth system have the potential for climate change. In response to these concerns, the GSFC Laboratory for Hydrospheric Processes has formed the Ocean Carbon Science Team (OCST) to contribute to greater understanding of the global ocean carbon cycle. The overall goals of the OCST are to: 1) detect changes in biological components of the ocean carbon cycle through remote sensing of biooptical properties, 2) refine understanding of ocean carbon uptake and sequestration through application of basic research results, new satellite algorithms, and improved model parameterizations, 3) develop and implement new sensors providing critical missing environmental information related to the oceanic carbon cycle and the flux of CO2 across the air-sea interface. The specific objectives of the OCST are to: 1) establish a 20-year time series of ocean color, 2) develop new remote sensing technologies, 3) validate ocean remote sensing observations, 4) conduct ocean carbon cycle scientific investigations directly related to remote sensing data, emphasizing physiological, empirical and coupled physical/biological models, satellite algorithm development and improvement, and analysis of satellite data sets. These research and mission objectives are intended to improve our understanding of global ocean carbon cycling and contribute to national goals by maximizing the use of remote sensing data.
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A dual isotope approach to isolate soil carbon pools of different turnover times
Torn, M. S.; Kleber, M.; Zavaleta, E. S.; ...
2013-12-10
Soils are globally significant sources and sinks of atmospheric CO 2. Increasing the resolution of soil carbon turnover estimates is important for predicting the response of soil carbon cycling to environmental change. We show that soil carbon turnover times can be more finely resolved using a dual isotope label like the one provided by elevated CO 2 experiments that use fossil CO 2. We modeled each soil physical fraction as two pools with different turnover times using the atmospheric 14C bomb spike in combination with the label in 14C and 13C provided by an elevated CO 2 experiment in amore » California annual grassland. In sandstone and serpentine soils, the light fraction carbon was 21–54% fast cycling with 2–9 yr turnover, and 36–79% slow cycling with turnover slower than 100 yr. This validates model treatment of the light fraction as active and intermediate cycling carbon. The dense, mineral-associated fraction also had a very dynamic component, consisting of ~7% fast-cycling carbon and ~93% very slow cycling carbon. Similarly, half the microbial biomass carbon in the sandstone soil was more than 5 yr old, and 40% of the carbon respired by microbes had been fixed more than 5 yr ago. Resolving each density fraction into two pools revealed that only a small component of total soil carbon is responsible for most CO 2 efflux from these soils. In the sandstone soil, 11% of soil carbon contributes more than 90% of the annual CO 2 efflux. The fact that soil physical fractions, designed to isolate organic material of roughly homogeneous physico-chemical state, contain material of dramatically different turnover times is consistent with recent observations of rapid isotope incorporation into seemingly stable fractions and with emerging evidence for hot spots or micro-site variation of decomposition within the soil matrix. Predictions of soil carbon storage using a turnover time estimated with the assumption of a single pool per density fraction would greatly overestimate the near-term response to changes in productivity or decomposition rates. Therefore, these results suggest a slower initial change in soil carbon storage due to environmental change than has been assumed by simpler (one-pool) mass balance calculations.« less
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Nitrogen Deposition: A Component of Global Change Analyses
DOE Office of Scientific and Technical Information (OSTI.GOV)
Norby, Richard J.
1997-12-31
The global cycles of carbon and nitrogen are being perturbed by human activities that increase the transfer from large pools of nonreactive forms of the elements to reactive forms that are essential to the functioning of the terrestrial biosphere. The cycles are closely linked at all scales, and global change analyses must consider carbon and nitrogen cycles together. The increasing amount of nitrogen originating from fossil fuel combustion and deposited to terrestrial ecosystems as nitrogen oxides could increase the capacity of ecosystems to sequester carbon thereby removing some of the excess carbon dioxide from the atmosphere and slowing the developmentmore » of greenhouse warming. Several global and ecosystem models have calculated the amount of carbon sequestration that can be attributed to nitrogen deposition based on assumptions about the allocation of nitrogen among ecosystem components with different carbon-nitrogen ratios. They support the premise that nitrogen deposition is responsible for a an increasing terrestrial carbon sink since industrialization began, but there are large uncertainties related to the continued capacity of ecosystems to retain exogenous nitrogen. Whether terrestrial ecosystems continue to sequester additional carbon will depend in part on their response to increasing atmospheric carbon dioxide concentrations, which is widely thought to be constrained by limited nitrogen availability. Ecosystem models generally support the conclusion that the responses of ecosystems to increasing concentrations of carbon dioxide will be larger, and the range of possible responses will be wider, in ecosystems with increased nitrogen inputs originating as atmospheric deposition.« less
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Benchmark carbon stocks from old-growth forests in northern New England, USA
Coeli M. Hoover; William B. Leak; Brian G. Keel
2012-01-01
Forests world-wide are recognized as important components of the global carbon cycle. Carbon sequestration has become a recognized forest management objective, but the full carbon storage potential of forests is not well understood. The premise of this study is that old-growth forests can be expected to provide a reasonable estimate of the upper limits of carbon...
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Nicholas A. Sutfin; Ellen E. Wohl; Kathleen A. Dwire
2016-01-01
Rivers are dynamic components of the terrestrial carbon cycle and provide important functions in ecosystem processes. Although rivers act as conveyers of carbon to the oceans, rivers also retain carbon within riparian ecosystems along floodplains, with potential for long-term (> 102 years) storage. Research in ecosystem processing emphasizes the...
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DOE Office of Scientific and Technical Information (OSTI.GOV)
Graber, J.; Amthor, J.; Dahlman, R.
2008-12-01
One of the most daunting challenges facing science in the 21st Century is to predict how Earth's ecosystems will respond to global climate change. The global carbon cycle plays a central role in regulating atmospheric carbon dioxide (CO{sub 2}) levels and thus Earth's climate, but our basic understanding of the myriad of tightly interlinked biological processes that drive the global carbon cycle remains limited at best. Whether terrestrial and ocean ecosystems will capture, store, or release carbon is highly dependent on how changing climate conditions affect processes performed by the organisms that form Earth's biosphere. Advancing our knowledge of biologicalmore » components of the global carbon cycle is thus crucial to predicting potential climate change impacts, assessing the viability of climate change adaptation and mitigation strategies, and informing relevant policy decisions. Global carbon cycling is dominated by the paired biological processes of photosynthesis and respiration. Photosynthetic plants and microbes of Earth's land-masses and oceans use solar energy to transform atmospheric CO{sub 2} into organic carbon. The majority of this organic carbon is rapidly consumed by plants or microbial decomposers for respiration and returned to the atmosphere as CO{sub 2}. Coupling between the two processes results in a near equilibrium between photosynthesis and respiration at the global scale, but some fraction of organic carbon also remains in stabilized forms such as biomass, soil, and deep ocean sediments. This process, known as carbon biosequestration, temporarily removes carbon from active cycling and has thus far absorbed a substantial fraction of anthropogenic carbon emissions.« less
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NASA Astrophysics Data System (ADS)
Brune, S.; Williams, S.; Müller, D.
2017-12-01
The deep carbon cycle links the carbon content of crust and mantle to Earth's surface: extensional plate boundaries and arc volcanoes release CO2 to the ocean and atmosphere while subducted lithosphere carries carbon back into the mantle. The length of extensional and convergent plate boundaries therefore exerts first-order control on solid Earth CO2 degassing rates. Here we provide a global census of plate boundary length for the last 200 million years. Focusing on rift systems, we find that the most extensive rift phase during the fragmentation of Pangea occurred in the Jurassic/Early Cretaceous with more than 50.000 km of simultaneously active continental rifts. During the Late Cretaceous, in the aftermath of this pervasive rift episode, the global rift length dropped by 60% to 20,000 km. We further find that a second pronounced rift episode with global rift lengths of up to 30,000 km started in Eocene times. A close geological link between CO2 degassing and faulting has been documented in currently active rift systems worldwide. Regional-scale CO2 flux densities at rift segments in Africa, Europe, and New Zealand feature an annual average value of 200 t of CO2 per km2. Assuming that the release of CO2 scales with rift length, we show that rift-related CO2 degassing rates during the two major Mesozoic and Cenozoic rift episodes reached more than 300% of present-day values. Most importantly, the timing of enhanced CO2 degassing from continental rifts correlates with two well-known periods of elevated atmospheric CO2 in the Mesozoic and Cenozoic as evidenced by multiple independent proxy indicators. Compiling the length of other plate boundaries (mid-ocean ridges, subduction zones, continental arcs) through time, we do not reproduce such a correlation. Finally, we conduct numerical carbon cycle models that account for key feedback-mechanisms of the long-term carbon cycle. We find that only those models that feature a strong rift degassing component reproduce the timing and amplitude of the paleo-CO2 record. We therefore suggest that rift-related degassing constitutes a key component of the deep carbon cycle.
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Dali Guo; Harbin Li; Robert J. Mitchell; Han Wenxuan; Joseph J. Hendricks; Timothy J. Fahey; Ronald L. Hendrick
2008-01-01
Fine roots constitute a large and dynamic component of the carbon cycles of terrestrial ecosystems. The reported fivefold discrepancy in turnover estimates between median longevity (ML) from minirhizotrons and mean residence time (MRT) using carbon isotopes may have global consequences.
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Estimation of forest canopy nitrogen concentration. Chapter 15
Marie-Louise Smith; David Y. Hollinger; Scott Ollinger
2008-01-01
The ability to detect patterns of carbon assimilation by vegetation is a key component of the North American Carbon Program. Because photosynthetic potential is strongly related to biochemical constituents such as nitrogen and chlorophyll concentrations in foliage, the ability to incorporate canopy chemistry into landscape- to regional-scale carbon cycling research...
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NASA Astrophysics Data System (ADS)
Matveev, A.; Matthews, H. D.
2009-04-01
Carbon fluxes from land conversion are among the most uncertain variables in our understanding of the contemporary carbon cycle, which limits our ability to estimate both the total human contribution to current climate forcing and the net effect of terrestrial biosphere changes on atmospheric CO2 increases. The current generation of coupled climate-carbon models have made significant progress in simulating the coupled climate and carbon cycle response to anthropogenic CO2 emissions, but do not typically include land-use change as a dynamic component of the simulation. In this work we have incorporated a book-keeping land-use carbon accounting model into the University of Victoria Earth System Climate Model (UVic ESCM), and intermediate-complexity coupled climate-carbon model. The terrestrial component of the UVic ESCM allows an aerial competition of five plant functional types (PFTs) in response to climatic conditions and area availability, and tracks the associated changes in affected carbon pools. In order to model CO2 emissions from land conversion in the terrestrial component of the model, we calculate the allocation of carbon to short and long-lived wood products following specified land-cover change, and use varying decay timescales to estimate CO2 emissions. We use recently available spatial datasets of both crop and pasture distributions to drive a series of transient simulations and estimate the net contribution of human land-use change to historical carbon emissions and climate change.
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Rachel A. Loehman; Elizabeth Reinhardt; Karin L. Riley
2014-01-01
Wildfires are an important component of the terrestrial carbon cycle and one of the main pathways for movement of carbon from the land surface to the atmosphere. Fires have received much attention in recent years as potential catalysts for shifting landscapes from carbon sinks to carbon sources. Unless structural or functional ecosystem shifts occur, net carbon balance...
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Nonautonomous linear system of the terrestrial carbon cycle
NASA Astrophysics Data System (ADS)
Luo, Y.
2012-12-01
Carbon cycle has been studied by uses of observation through various networks, field and laboratory experiments, and simulation models. Much less has been done on theoretical thinking and analysis to understand fundament properties of carbon cycle and then guide observatory, experimental, and modeling research. This presentation is to explore what would be the theoretical properties of terrestrial carbon cycle and how those properties can be used to make observatory, experimental, and modeling research more effective. Thousands of published data sets from litter decomposition and soil incubation studies almost all indicate that decay processes of litter and soil organic carbon can be well described by first order differential equations with one or more pools. Carbon pool dynamics in plants and soil after disturbances (e.g., wildfire, clear-cut of forests, and plows of soil for cropping) and during natural recovery or ecosystem restoration also exhibit characteristics of first-order linear systems. Thus, numerous lines of empirical evidence indicate that the terrestrial carbon cycle can be adequately described as a nonautonomous linear system. The linearity reflects the nature of the carbon cycle that carbon, once fixed by photosynthesis, is linearly transferred among pools within an ecosystem. The linear carbon transfer, however, is modified by nonlinear functions of external forcing variables. In addition, photosynthetic carbon influx is also nonlinearly influenced by external variables. This nonautonomous linear system can be mathematically expressed by a first-order linear ordinary matrix equation. We have recently used this theoretical property of terrestrial carbon cycle to develop a semi-analytic solution of spinup. The new methods have been applied to five global land models, including NCAR's CLM and CABLE models and can computationally accelerate spinup by two orders of magnitude. We also use this theoretical property to develop an analytic framework to decompose modeled carbon cycle into a few traceable components so as to facilitate model intercompsirosn, benchmark analysis, and data assimilation of global land models.
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Measurement and importance of dissolved organic carbon. Chapter 13
Randall Kolka; Peter Weishampel; Mats Froberg
2008-01-01
The flux of dissolved organic carbon (DOC) from an ecosystem can be a significant component of carbon (C) budgets especially in watersheds containing wetlands. Although internal ecosystem cycling of DOC is generally greater than the fluxes to ground or surface waters, it is the transport out of the system that is a main research focus for carbon accounting. In...
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USDA-ARS?s Scientific Manuscript database
Soil carbon dioxide (CO2) flux is an important component of the terrestrial carbon cycle. Accurate measurements of soil CO2 flux aids determinations of carbon budgets. In this study, we investigated soil CO2 fluxes with time and depth and above ground CO2 fluxes in a bare field. CO2 concentrations w...
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USDA-ARS?s Scientific Manuscript database
Resolving uncertainty in the carbon cycle is paramount to refining climate predictions. Soil organic carbon (SOC) is a major component of terrestrial C pools, and accuracy of SOC estimates are only as good as the measurements and assumptions used to obtain them. Dryland soils account for a substanti...
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Sonja N. Oswalt; Thomas J. Brandeis
2008-01-01
Dead wood is a substantial carbon stock in terrestrial forest ecosystems and hence a critical component of global carbon cycles. Given the limited amounts of dead wood biomass and carbon stock information for Caribbean forests, our objectives were to: (1) describe the relative contribution of down woody materials (DWM) to carbon stocks on the island of St. John; (2)...
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Sonja N. Oswalt; Thomas J. Brandeis
2008-01-01
Dead wood is a substantial carbon stock in terrestrial forest ecosystems and hence a critical component of global carbon cycles. Given the limited amounts of dead wood biomass and carbon stock information for Caribbean forests, our objectives were to: (1) describe the relative contribution of down woody materials (DWM) to carbon stocks on the island of St. John; (2)...
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Bloom, A. Anthony; Exbrayat, Jean-François; van der Velde, Ivar R.; Feng, Liang; Williams, Mathew
2016-01-01
The terrestrial carbon cycle is currently the least constrained component of the global carbon budget. Large uncertainties stem from a poor understanding of plant carbon allocation, stocks, residence times, and carbon use efficiency. Imposing observational constraints on the terrestrial carbon cycle and its processes is, therefore, necessary to better understand its current state and predict its future state. We combine a diagnostic ecosystem carbon model with satellite observations of leaf area and biomass (where and when available) and soil carbon data to retrieve the first global estimates, to our knowledge, of carbon cycle state and process variables at a 1° × 1° resolution; retrieved variables are independent from the plant functional type and steady-state paradigms. Our results reveal global emergent relationships in the spatial distribution of key carbon cycle states and processes. Live biomass and dead organic carbon residence times exhibit contrasting spatial features (r = 0.3). Allocation to structural carbon is highest in the wet tropics (85–88%) in contrast to higher latitudes (73–82%), where allocation shifts toward photosynthetic carbon. Carbon use efficiency is lowest (0.42–0.44) in the wet tropics. We find an emergent global correlation between retrievals of leaf mass per leaf area and leaf lifespan (r = 0.64–0.80) that matches independent trait studies. We show that conventional land cover types cannot adequately describe the spatial variability of key carbon states and processes (multiple correlation median = 0.41). This mismatch has strong implications for the prediction of terrestrial carbon dynamics, which are currently based on globally applied parameters linked to land cover or plant functional types. PMID:26787856
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Simulated Carbon Cycling in a Model Microbial Mat.
NASA Astrophysics Data System (ADS)
Decker, K. L.; Potter, C. S.
2006-12-01
We present here the novel addition of detailed organic carbon cycling to our model of a hypersaline microbial mat ecosystem. This ecosystem model, MBGC (Microbial BioGeoChemistry), simulates carbon fixation through oxygenic and anoxygenic photosynthesis, and the release of C and electrons for microbial heterotrophs via cyanobacterial exudates and also via a pool of dead cells. Previously in MBGC, the organic portion of the carbon cycle was simplified into a black-box rate of accumulation of simple and complex organic compounds based on photosynthesis and mortality rates. We will discuss the novel inclusion of fermentation as a source of carbon and electrons for use in methanogenesis and sulfate reduction, and the influence of photorespiration on labile carbon exudation rates in cyanobacteria. We will also discuss the modeling of decomposition of dead cells and the ultimate release of inorganic carbon. The detailed modeling of organic carbon cycling is important to the accurate representation of inorganic carbon flux through the mat, as well as to accurate representation of growth models of the heterotrophs under different environmental conditions. Because the model ecosystem is an analog of ancient microbial mats that had huge impacts on the atmosphere of early earth, this MBGC can be useful as a biological component to either early earth models or models of other planets that potentially harbor life.
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Towards a more complete SOCCR: Establishing a Coastal Carbon Data Network
NASA Astrophysics Data System (ADS)
Pidgeon, E.; Howard, J.; Tang, J.; Kroeger, K. D.; Windham-Myers, L.
2015-12-01
The 2007 State of the Carbon Cycle Report (SOCCR) was highly influential in ensuring components of the carbon cycle were accounted for in national policy and related management. However, while SOCCR detailed the significance of North American coastal wetlands, it was not until recently that leading governments began to fully recognized these ecosystems for their carbon sequestration and storage capacity and hence the significant role coastal ecosystems can play in GHG emission reductions strategies, offset mechanisms, coastal management strategies and climate mitigation policy. The new attention on coastal carbon systems has exposed limitations in terms of data availability and data quality, as well as insufficient knowledge of coastal carbon distributions, characteristics and coastal carbon cycle processes. In addition to restricting scientific progress, lack of comprehensive, comparable, and quality-controlled coastal carbon data is hindering progress towards carbon based conservation and coastal management. To directly address those limitations, we are developing a Global Science and Data Network for Coastal "Blue" Carbon, with support from the Carbon Cycle Interagency Working Group. Goals include: • Improving basic and applied science on carbon and GHG cycling in vegetated coastal ecosystems; • Supporting a coastal carbon and associated GHG data archive for use by the science community, coastal and climate practitioners and other data users; • Building the capacity of coastal carbon stakeholders globally to collect and interpret high quality coastal carbon science and data; • Providing a forum and mechanism to promote exchange and collaboration between scientists and coastal carbon data users globally; and • Outreach activities to ensure the best available data are globally accessible and that science is responsive to the needs of coastal managers and policy-makers.
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Biogeochemical carbon coupling influences global precipitation in geoengineering experiments
NASA Astrophysics Data System (ADS)
Fyfe, J. C.; Cole, J. N. S.; Arora, V. K.; Scinocca, J. F.
2013-02-01
Abstract Climate model studies in which CO2-induced global warming is offset by engineered decreases of incoming solar radiation are generally robust in their prediction of reduced amounts of global precipitation. While this precipitation response has been explained on the basis of changes in net radiation controlling evaporative processes at the surface, there has been relatively little consideration of the relative role of biogeochemical carbon-cycle interactions. To address this issue, we employ an Earth System Model that includes oceanic and terrestrial carbon components to isolate the impact of biogeochemical carbon coupling on the precipitation response in geoengineering experiments for two types of solar radiation management. We show that carbon coupling is responsible for a large fraction of the global precipitation reduction in such geoengineering experiments and that the primary effect comes from reduced transpiration through the leaves of plants and trees in the terrestrial component of the carbon cycle due to elevated CO2. Our results suggest that biogeochemical interactions are as important as changes in net radiation and that climate models that do not account for such carbon coupling may significantly underestimate precipitation reductions in a geoengineered world.</p> </li> <li> <p><a target="_blank" rel="noopener noreferrer" onclick="trackOutboundLink('https://www.fs.usda.gov/treesearch/pubs/50435','TREESEARCH'); return false;" href="https://www.fs.usda.gov/treesearch/pubs/50435"><span>Estimating carbon in forest soils of the United States using the national forest inventory</span></a></p> <p><a target="_blank" rel="noopener noreferrer" href="http://www.fs.usda.gov/treesearch/">Treesearch</a></p> <p>Grant M. Domke; Charles H. (Hobie) Perry; Brian F. Walters; Christopher W. Woodall; Lucas E. Nave; Chris Swanston</p> <p>2015-01-01</p> <p>Soil organic carbon (SOC) is the largest terrestrial carbon (C) sink on earth and management of this pool is a critical component of global efforts to mitigate atmospheric C concentrations. Soil organic carbon is also a key indicator of soil quality as it affects essential biological, chemical, and physical soil functions such as nutrient cycling, water retention, and...</p> </li> <li> <p><a target="_blank" rel="noopener noreferrer" onclick="trackOutboundLink('https://www.pubmedcentral.nih.gov/articlerender.fcgi?tool=pmcentrez&artid=4423203','PMC'); return false;" href="https://www.pubmedcentral.nih.gov/articlerender.fcgi?tool=pmcentrez&artid=4423203"><span>Hyperdominance in Amazonian forest carbon cycling</span></a></p> <p><a target="_blank" rel="noopener noreferrer" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?DB=pmc">PubMed Central</a></p> <p>Fauset, Sophie; Johnson, Michelle O.; Gloor, Manuel; Baker, Timothy R.; Monteagudo M., Abel; Brienen, Roel J.W.; Feldpausch, Ted R.; Lopez-Gonzalez, Gabriela; Malhi, Yadvinder; ter Steege, Hans; Pitman, Nigel C.A.; Baraloto, Christopher; Engel, Julien; Pétronelli, Pascal; Andrade, Ana; Camargo, José Luís C.; Laurance, Susan G.W.; Laurance, William F.; Chave, Jerôme; Allie, Elodie; Vargas, Percy Núñez; Terborgh, John W.; Ruokolainen, Kalle; Silveira, Marcos; Aymard C., Gerardo A.; Arroyo, Luzmila; Bonal, Damien; Ramirez-Angulo, Hirma; Araujo-Murakami, Alejandro; Neill, David; Hérault, Bruno; Dourdain, Aurélie; Torres-Lezama, Armando; Marimon, Beatriz S.; Salomão, Rafael P.; Comiskey, James A.; Réjou-Méchain, Maxime; Toledo, Marisol; Licona, Juan Carlos; Alarcón, Alfredo; Prieto, Adriana; Rudas, Agustín; van der Meer, Peter J.; Killeen, Timothy J.; Marimon Junior, Ben-Hur; Poorter, Lourens; Boot, Rene G.A.; Stergios, Basil; Torre, Emilio Vilanova; Costa, Flávia R.C.; Levis, Carolina; Schietti, Juliana; Souza, Priscila; Groot, Nikée; Arets, Eric; Moscoso, Victor Chama; Castro, Wendeson; Coronado, Euridice N. Honorio; Peña-Claros, Marielos; Stahl, Clement; Barroso, Jorcely; Talbot, Joey; Vieira, Ima Célia Guimarães; van der Heijden, Geertje; Thomas, Raquel; Vos, Vincent A.; Almeida, Everton C.; Davila, Esteban Álvarez; Aragão, Luiz E.O.C.; Erwin, Terry L.; Morandi, Paulo S.; de Oliveira, Edmar Almeida; Valadão, Marco B.X.; Zagt, Roderick J.; van der Hout, Peter; Loayza, Patricia Alvarez; Pipoly, John J.; Wang, Ophelia; Alexiades, Miguel; Cerón, Carlos E.; Huamantupa-Chuquimaco, Isau; Di Fiore, Anthony; Peacock, Julie; Camacho, Nadir C. Pallqui; Umetsu, Ricardo K.; de Camargo, Plínio Barbosa; Burnham, Robyn J.; Herrera, Rafael; Quesada, Carlos A.; Stropp, Juliana; Vieira, Simone A.; Steininger, Marc; Rodríguez, Carlos Reynel; Restrepo, Zorayda; Muelbert, Adriane Esquivel; Lewis, Simon L.; Pickavance, Georgia C.; Phillips, Oliver L.</p> <p>2015-01-01</p> <p>While Amazonian forests are extraordinarily diverse, the abundance of trees is skewed strongly towards relatively few ‘hyperdominant' species. In addition to their diversity, Amazonian trees are a key component of the global carbon cycle, assimilating and storing more carbon than any other ecosystem on Earth. Here we ask, using a unique data set of 530 forest plots, if the functions of storing and producing woody carbon are concentrated in a small number of tree species, whether the most abundant species also dominate carbon cycling, and whether dominant species are characterized by specific functional traits. We find that dominance of forest function is even more concentrated in a few species than is dominance of tree abundance, with only ≈1% of Amazon tree species responsible for 50% of carbon storage and productivity. Although those species that contribute most to biomass and productivity are often abundant, species maximum size is also influential, while the identity and ranking of dominant species varies by function and by region. PMID:25919449</p> </li> <li> <p><a target="_blank" rel="noopener noreferrer" onclick="trackOutboundLink('https://www.ncbi.nlm.nih.gov/pubmed/25919449','PUBMED'); return false;" href="https://www.ncbi.nlm.nih.gov/pubmed/25919449"><span>Hyperdominance in Amazonian forest carbon cycling.</span></a></p> <p><a target="_blank" rel="noopener noreferrer" href="https://www.ncbi.nlm.nih.gov/entrez/query.fcgi?DB=pubmed">PubMed</a></p> <p>Fauset, Sophie; Johnson, Michelle O; Gloor, Manuel; Baker, Timothy R; Monteagudo M, Abel; Brienen, Roel J W; Feldpausch, Ted R; Lopez-Gonzalez, Gabriela; Malhi, Yadvinder; ter Steege, Hans; Pitman, Nigel C A; Baraloto, Christopher; Engel, Julien; Pétronelli, Pascal; Andrade, Ana; Camargo, José Luís C; Laurance, Susan G W; Laurance, William F; Chave, Jerôme; Allie, Elodie; Vargas, Percy Núñez; Terborgh, John W; Ruokolainen, Kalle; Silveira, Marcos; Aymard C, Gerardo A; Arroyo, Luzmila; Bonal, Damien; Ramirez-Angulo, Hirma; Araujo-Murakami, Alejandro; Neill, David; Hérault, Bruno; Dourdain, Aurélie; Torres-Lezama, Armando; Marimon, Beatriz S; Salomão, Rafael P; Comiskey, James A; Réjou-Méchain, Maxime; Toledo, Marisol; Licona, Juan Carlos; Alarcón, Alfredo; Prieto, Adriana; Rudas, Agustín; van der Meer, Peter J; Killeen, Timothy J; Marimon Junior, Ben-Hur; Poorter, Lourens; Boot, Rene G A; Stergios, Basil; Torre, Emilio Vilanova; Costa, Flávia R C; Levis, Carolina; Schietti, Juliana; Souza, Priscila; Groot, Nikée; Arets, Eric; Moscoso, Victor Chama; Castro, Wendeson; Coronado, Euridice N Honorio; Peña-Claros, Marielos; Stahl, Clement; Barroso, Jorcely; Talbot, Joey; Vieira, Ima Célia Guimarães; van der Heijden, Geertje; Thomas, Raquel; Vos, Vincent A; Almeida, Everton C; Davila, Esteban Álvarez; Aragão, Luiz E O C; Erwin, Terry L; Morandi, Paulo S; de Oliveira, Edmar Almeida; Valadão, Marco B X; Zagt, Roderick J; van der Hout, Peter; Loayza, Patricia Alvarez; Pipoly, John J; Wang, Ophelia; Alexiades, Miguel; Cerón, Carlos E; Huamantupa-Chuquimaco, Isau; Di Fiore, Anthony; Peacock, Julie; Camacho, Nadir C Pallqui; Umetsu, Ricardo K; de Camargo, Plínio Barbosa; Burnham, Robyn J; Herrera, Rafael; Quesada, Carlos A; Stropp, Juliana; Vieira, Simone A; Steininger, Marc; Rodríguez, Carlos Reynel; Restrepo, Zorayda; Muelbert, Adriane Esquivel; Lewis, Simon L; Pickavance, Georgia C; Phillips, Oliver L</p> <p>2015-04-28</p> <p>While Amazonian forests are extraordinarily diverse, the abundance of trees is skewed strongly towards relatively few 'hyperdominant' species. In addition to their diversity, Amazonian trees are a key component of the global carbon cycle, assimilating and storing more carbon than any other ecosystem on Earth. Here we ask, using a unique data set of 530 forest plots, if the functions of storing and producing woody carbon are concentrated in a small number of tree species, whether the most abundant species also dominate carbon cycling, and whether dominant species are characterized by specific functional traits. We find that dominance of forest function is even more concentrated in a few species than is dominance of tree abundance, with only ≈1% of Amazon tree species responsible for 50% of carbon storage and productivity. Although those species that contribute most to biomass and productivity are often abundant, species maximum size is also influential, while the identity and ranking of dominant species varies by function and by region.</p> </li> <li> <p><a target="_blank" rel="noopener noreferrer" onclick="trackOutboundLink('http://adsabs.harvard.edu/abs/2014AGUFMED33A3502Z','NASAADS'); return false;" href="http://adsabs.harvard.edu/abs/2014AGUFMED33A3502Z"><span>Moving Carbon, Changing Earth: Bringing the Carbon Cycle to Life</span></a></p> <p><a target="_blank" rel="noopener noreferrer" href="http://adsabs.harvard.edu/abstract_service.html">NASA Astrophysics Data System (ADS)</a></p> <p>Zabel, I.; Duggan-Haas, D.; Ross, R. M.; Stricker, B.; Mahowald, N. M.</p> <p>2014-12-01</p> <p>The carbon cycle presents challenges to researchers - in how to understand the complex interactions of fluxes, reservoirs, and systems - and to outreach professionals - in how to get across the complexity of the carbon cycle and still make it accessible to the public. At Cornell University and the Museum of the Earth in Ithaca, NY, researchers and outreach staff tackled these challenges together through a 2013 temporary museum exhibition: Moving Carbon, Changing Earth. Moving Carbon, Changing Earth introduced visitors to the world of carbon and its effect on every part of our lives. The exhibit was the result of the broader impacts portion of an NSF grant awarded to Natalie Mahowald, Professor in the Department of Earth and Atmospheric Sciences at Cornell University, who has been working with a team to improve simulations of regional and decadal variability in the carbon cycle. Within the exhibition, visitors used systems thinking to understand the distribution of carbon in and among Earth's systems, learning how (and how quickly or slowly) carbon moves between and within these systems, the relative scale of different reservoirs, and how carbon's movement changes climate and other environmental dynamics. Five interactive stations represented the oceans, lithosphere, atmosphere, biosphere, and a mystery reservoir. Puzzles, videos, real specimens, and an interview with Mahowald clarified and communicated the complexities of the carbon cycle. In this talk we'll present background information on Mahowald's research as well as photos of the exhibition and discussion of the components and motivations behind them, showing examples of innovative ways to bring a complex topic to life for museum visitors.</p> </li> <li> <p><a target="_blank" rel="noopener noreferrer" onclick="trackOutboundLink('https://www.fs.usda.gov/treesearch/pubs/30084','TREESEARCH'); return false;" href="https://www.fs.usda.gov/treesearch/pubs/30084"><span>Estimates of forest canopy height and aboveground biomass using ICESat.</span></a></p> <p><a target="_blank" rel="noopener noreferrer" href="http://www.fs.usda.gov/treesearch/">Treesearch</a></p> <p>Michael A. Lefsky; David J. Harding; Michael Keller; Warren B. Cohen; Claudia C. Carabajal; Fernando Del Bom Espirito-Santo; Maria O. Hunter; Raimundo de Oliveira Jr.</p> <p>2005-01-01</p> <p>Exchange of carbon between forests and the atmosphere is a vital component of the global carbon cycle. Satellite laser altimetry has a unique capability for estimating forest canopy height, which has a direct and increasingly well understood relationship to aboveground carbon storage. While the Geoscience Laser Altimeter System (GLAS) onboard the Ice, Cloud and land...</p> </li> <li> <p><a target="_blank" rel="noopener noreferrer" onclick="trackOutboundLink('https://ntrs.nasa.gov/search.jsp?R=19890059620&hterms=phenolic&qs=Ntx%3Dmode%2Bmatchall%26Ntk%3DAll%26N%3D0%26No%3D50%26Ntt%3Dphenolic','NASA-TRS'); return false;" href="https://ntrs.nasa.gov/search.jsp?R=19890059620&hterms=phenolic&qs=Ntx%3Dmode%2Bmatchall%26Ntk%3DAll%26N%3D0%26No%3D50%26Ntt%3Dphenolic"><span>Process modeling for carbon-phenolic nozzle materials</span></a></p> <p><a target="_blank" rel="noopener noreferrer" href="http://ntrs.nasa.gov/search.jsp">NASA Technical Reports Server (NTRS)</a></p> <p>Letson, Mischell A.; Bunker, Robert C.; Remus, Walter M., III; Clinton, R. G.</p> <p>1989-01-01</p> <p>A thermochemical model based on the SINDA heat transfer program is developed for carbon-phenolic nozzle material processes. The model can be used to optimize cure cycles and to predict material properties based on the types of materials and the process by which these materials are used to make nozzle components. Chemical kinetic constants for Fiberite MX4926 were determined so that optimization of cure cycles for the current Space Shuttle Solid Rocket Motor nozzle rings can be determined.</p> </li> <li> <p><a target="_blank" rel="noopener noreferrer" onclick="trackOutboundLink('https://www.osti.gov/servlets/purl/1234261','SCIGOV-STC'); return false;" href="https://www.osti.gov/servlets/purl/1234261"><span></span></a></p> <p><a target="_blank" rel="noopener noreferrer" href="http://www.osti.gov/search">DOE Office of Scientific and Technical Information (OSTI.GOV)</a></p> <p>Hollinger, David; Davidson, E.; Dail, D. B.</p> <p></p> <p>This report provides and overview of the work carried out and lists the products produced under the terms of agreement SC0005578 with the USDA Forest Service. This relates to scientific investigation of the carbon cycle at the Howland Forest AmeriFlux site located in central Maine, USDA. The overall goal of this work was to understand the various (and interacting) impacts of a changing climate on carbon cycling at the Howland AmeriFlux site, representative of an important component of the North American boreal forest.</p> </li> <li> <p><a target="_blank" rel="noopener noreferrer" onclick="trackOutboundLink('https://www.osti.gov/servlets/purl/1389478','SCIGOV-DOEDE'); return false;" href="https://www.osti.gov/servlets/purl/1389478"><span>Global Carbon Project: the Global Carbon Budget 2015 (V.1.0., issued Nov. 2015 and V.1.1, issued Dec. 2015)</span></a></p> <p><a target="_blank" rel="noopener noreferrer" href="http://www.osti.gov/dataexplorer">DOE Data Explorer</a></p> <p>Le Quere, C. [University of East Anglia, Norwich UK; Moriarty, R. [University of East Anglia, Norwich UK; Andrew, R. M. [Univ. of Oslo (Norway); Canadell, J. G. [Commonwealth Scientific and Industrial Research Organization (CSIRO) Oceans and Atmosphere, Canberra ACT (Australia); Sitch, S. [University of Exeter, Exter UK; Boden, T. A. [Oak Ridge National Lab. (ORNL), Oak Ridge, TN (United States) Carbon Dioxide Information Analysis Center (CDIAC); al., et</p> <p>2015-01-01</p> <p>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.</p> </li> <li> <p><a target="_blank" rel="noopener noreferrer" onclick="trackOutboundLink('http://adsabs.harvard.edu/abs/2014AGUFM.B23C0215A','NASAADS'); return false;" href="http://adsabs.harvard.edu/abs/2014AGUFM.B23C0215A"><span>Global Carbon Cycle Modeling in GISS ModelE2 GCM</span></a></p> <p><a target="_blank" rel="noopener noreferrer" href="http://adsabs.harvard.edu/abstract_service.html">NASA Astrophysics Data System (ADS)</a></p> <p>Aleinov, I. D.; Kiang, N. Y.; Romanou, A.; Romanski, J.</p> <p>2014-12-01</p> <p>Consistent and accurate modeling of the Global Carbon Cycle remains one of the main challenges for the Earth System Models. NASA Goddard Institute for Space Studies (GISS) ModelE2 General Circulation Model (GCM) was recently equipped with a complete Global Carbon Cycle algorithm, consisting of three integrated components: Ent Terrestrial Biosphere Model (Ent TBM), Ocean Biogeochemistry Module and atmospheric CO2 tracer. Ent TBM provides CO2 fluxes from the land surface to the atmosphere. Its biophysics utilizes the well-known photosynthesis functions of Farqhuar, von Caemmerer, and Berry and Farqhuar and von Caemmerer, and stomatal conductance of Ball and Berry. Its phenology is based on temperature, drought, and radiation fluxes, and growth is controlled via allocation of carbon from labile carbohydrate reserve storage to different plant components. Soil biogeochemistry is based on the Carnegie-Ames-Stanford (CASA) model of Potter et al. Ocean biogeochemistry module (the NASA Ocean Biogeochemistry Model, NOBM), computes prognostic distributions for biotic and abiotic fields that influence the air-sea flux of CO2 and the deep ocean carbon transport and storage. Atmospheric CO2 is advected with a quadratic upstream algorithm implemented in atmospheric part of ModelE2. Here we present the results for pre-industrial equilibrium and modern transient simulations and provide comparison to available observations. We also discuss the process of validation and tuning of particular algorithms used in the model.</p> </li> <li> <p><a target="_blank" rel="noopener noreferrer" onclick="trackOutboundLink('http://adsabs.harvard.edu/abs/2017GeCoA.208..102Z','NASAADS'); return false;" href="http://adsabs.harvard.edu/abs/2017GeCoA.208..102Z"><span>Constraining the sources and cycling of dissolved organic carbon in a large oligotrophic lake using radiocarbon analyses</span></a></p> <p><a target="_blank" rel="noopener noreferrer" href="http://adsabs.harvard.edu/abstract_service.html">NASA Astrophysics Data System (ADS)</a></p> <p>Zigah, Prosper K.; Minor, Elizabeth C.; McNichol, Ann P.; Xu, Li; Werne, Josef P.</p> <p>2017-07-01</p> <p>We measured the concentrations and isotopic compositions of solid phase extracted (SPE) dissolved organic carbon (DOC) and high molecular weight (HMW) DOC and their constituent organic components in order to better constrain the sources and cycling of DOC in a large oligotrophic lacustrine system (Lake Superior, North America). SPE DOC constituted a significant proportion (41-71%) of the lake DOC relative to HMW DOC (10-13%). Substantial contribution of 14C-depleted components to both SPE DOC (Δ14C = 25-43‰) and HMW DOC (Δ14C = 22-32‰) was evident during spring mixing, and depressed their radiocarbon values relative to the lake dissolved inorganic carbon (DIC; Δ14C ∼ 59‰). There was preferential removal of 14C-depleted (older) and thermally recalcitrant components from HMW DOC and SPE DOC in the summer. Contemporary photoautotrophic addition to HMW DOC was observed during summer stratification in contrast to SPE DOC, which decreased in concentration during stratification. Serial thermal oxidation radiocarbon analysis revealed a diversity of sources (both contemporary and older) within the SPE DOC, and also showed distinct components within the HMW DOC. The thermally labile components of HMW DOC were 14C-enriched and are attributed to heteropolysaccharides (HPS), peptides/amide and amino sugars (AMS) relative to the thermally recalcitrant components reflecting the presence of older material, perhaps carboxylic-rich alicyclic molecules (CRAM). The solvent extractable lipid-like fraction of HMW DOC was very 14C-depleted (as old as 1270-2320 14C years) relative to the carbohydrate-like and protein-like substances isolated by acid hydrolysis of HMW DOC. Our data constrain relative influences of contemporary DOC and old DOC, and DOC cycling in a modern freshwater ecosystem.</p> </li> </ol> <div class="pull-right"> <ul class="pagination"> <li><a href="#" onclick='return showDiv("page_1");'>«</a></li> <li><a href="#" onclick='return showDiv("page_1");'>1</a></li> <li><a href="#" onclick='return showDiv("page_2");'>2</a></li> <li class="active"><span>3</span></li> <li><a href="#" onclick='return showDiv("page_4");'>4</a></li> <li><a href="#" onclick='return showDiv("page_5");'>5</a></li> <li><a href="#" onclick='return showDiv("page_25");'>»</a></li> </ul> </div> </div><!-- col-sm-12 --> </div><!-- row --> </div><!-- page_3 --> <div id="page_4" class="hiddenDiv"> <div class="row"> <div class="col-sm-12"> <div class="pull-right"> <ul class="pagination"> <li><a href="#" onclick='return showDiv("page_1");'>«</a></li> <li><a href="#" onclick='return showDiv("page_2");'>2</a></li> <li><a href="#" onclick='return showDiv("page_3");'>3</a></li> <li class="active"><span>4</span></li> <li><a href="#" onclick='return showDiv("page_5");'>5</a></li> <li><a href="#" onclick='return showDiv("page_6");'>6</a></li> <li><a href="#" onclick='return showDiv("page_25");'>»</a></li> </ul> </div> </div> </div> <div class="row"> <div class="col-sm-12"> <ol class="result-class" start="61"> <li> <p><a target="_blank" rel="noopener noreferrer" onclick="trackOutboundLink('http://hdl.handle.net/2060/20140010290','NASA-TRS'); return false;" href="http://hdl.handle.net/2060/20140010290"><span>Definition, Capabilities, and Components of a Terrestrial Carbon Monitoring System</span></a></p> <p><a target="_blank" rel="noopener noreferrer" href="http://ntrs.nasa.gov/search.jsp">NASA Technical Reports Server (NTRS)</a></p> <p>West, Tristram O.; Brown, Molly E.; Duren, Riley M.; Ogle, Stephen M.; Moss, Richard H.</p> <p>2013-01-01</p> <p>Research efforts for effectively and consistently monitoring terrestrial carbon are increasing in number. As such, there is a need to define carbon monitoring and how it relates to carbon cycle science and carbon management. There is also a need to identify capabilities of a carbon monitoring system and the system components needed to develop the capabilities. Capabilities that enable the effective application of a carbon monitoring system for monitoring and management purposes may include: reconciling carbon stocks and fluxes, developing consistency across spatial and temporal scales, tracking horizontal movement of carbon, attribution of emissions to originating sources, cross-sectoral accounting, uncertainty quantification, redundancy and policy relevance. Focused research is needed to integrate these capabilities for sustained estimates of carbon stocks and fluxes. Additionally, if monitoring is intended to inform management decisions, management priorities should be considered prior to development of a monitoring system.</p> </li> <li> <p><a target="_blank" rel="noopener noreferrer" onclick="trackOutboundLink('http://adsabs.harvard.edu/abs/2015Nanot..26H5401C','NASAADS'); return false;" href="http://adsabs.harvard.edu/abs/2015Nanot..26H5401C"><span>Nitrogen-enriched carbon sheets derived from egg white by using expanded perlite template and its high-performance supercapacitors</span></a></p> <p><a target="_blank" rel="noopener noreferrer" href="http://adsabs.harvard.edu/abstract_service.html">NASA Astrophysics Data System (ADS)</a></p> <p>Chen, Jiucun; Liu, Yinqin; Li, Wenjun; Xu, Liqun; Yang, Huan; Li, Chang Ming</p> <p>2015-08-01</p> <p>Nitrogen-enriched carbon sheets were synthesized using egg white as a unique carbon source and expanded perlite as a novel template. The as-prepared material was further used as an electrode material for supercapacitor applications, demonstrating excellent supercapacitance with a maximum gravimetric specific capacitance of 302 F g-1 at 0.5 A g-1 in a 3-electrode setup for a sample carbonized at 850 °C and activated for 6 h. Moreover, the carbon sheet-based capacitor with 2-symmetric electrodes showed an excellent cycle life (2% loss at 0.1 A g-1 after 10 000 cycles). The excellent performance may be attributed to the combination of the 3D carbon structure and the highly concentrated doped nitrogen component from the natural egg source for superior pseudocapacitance.</p> </li> <li> <p><a target="_blank" rel="noopener noreferrer" onclick="trackOutboundLink('http://adsabs.harvard.edu/abs/2012AGUFM.B51B0492L','NASAADS'); return false;" href="http://adsabs.harvard.edu/abs/2012AGUFM.B51B0492L"><span>A climate sensitive model of carbon transfer through atmosphere, vegetation and soil in managed forest ecosystems</span></a></p> <p><a target="_blank" rel="noopener noreferrer" href="http://adsabs.harvard.edu/abstract_service.html">NASA Astrophysics Data System (ADS)</a></p> <p>Loustau, D.; Moreaux, V.; Bosc, A.; Trichet, P.; Kumari, J.; Rabemanantsoa, T.; Balesdent, J.; Jolivet, C.; Medlyn, B. E.; Cavaignac, S.; Nguyen-The, N.</p> <p>2012-12-01</p> <p>For predicting the future of the forest carbon cycle in forest ecosystems, it is necessary to account for both the climate and management impacts. Climate effects are significant not only at a short time scale but also at the temporal horizon of a forest life cycle e.g. through shift in atmospheric CO2 concentration, temperature and precipitation regimes induced by the enhanced greenhouse effect. Intensification of forest management concerns an increasing fraction of temperate and tropical forests and untouched forests represents only one third of the present forest area. Predicting tools are therefore needed to project climate and management impacts over the forest life cycle and understand the consequence of management on the forest ecosystem carbon cycle. This communication summarizes the structure, main components and properties of a carbon transfer model that describes the processes controlling the carbon cycle of managed forest ecosystems. The model, GO+, links three main components, (i) a module describing the vegetation-atmosphere mass and energy exchanges in 3D, (ii) a plant growth module and a (iii) soil carbon dynamics module in a consistent carbon scheme of transfer from atmosphere back into the atmosphere. It was calibrated and evaluated using observed data collected on coniferous and broadleaved forest stands. The model predicts the soil, water and energy balance of entire rotations of managed stands from the plantation to the final cut and according to a range of management alternatives. It accounts for the main soil and vegetation management operations such as soil preparation, understorey removal, thinnings and clearcutting. Including the available knowledge on the climatic sensitivity of biophysical and biogeochemical processes involved in atmospheric exchanges and carbon cycle of forest ecosystems, GO+ can produce long-term backward or forward simulations of forest carbon and water cycles under a range of climate and management scenarios. This model applications to the prediction and analysis of climate scenarios impacts on southwestern European forests underlines the role of management alternatives, precipitation regime, CO2 concentration and atmospheric humidity .Frequency of soil preparation operations and understorey management play a major role in controlling the net carbon flux into the atmosphere at the juvenile stage ( 0 to 10 y-old) whereas climate and rotation duration control the functioning of adult phase. The model predicts that a drier and warmer climate will reduce the forest productivity and deplete soil and carbon stocks in managed forest from Southwestern Europe within decades, such effects being amplified for most intensive management alternatives. This work was part of the European research project GHG-Europe (EU contract No. 244122) and the French national project FAST co-funded by the Ecology, Agriculture and Forestry Ministries and the Region Aquitaine.</p> </li> <li> <p><a target="_blank" rel="noopener noreferrer" onclick="trackOutboundLink('http://adsabs.harvard.edu/abs/2011JPS...196.4347S','NASAADS'); return false;" href="http://adsabs.harvard.edu/abs/2011JPS...196.4347S"><span>A comparison between molten carbonate fuel cells based hybrid systems using air and supercritical carbon dioxide Brayton cycles with state of the art technology</span></a></p> <p><a target="_blank" rel="noopener noreferrer" href="http://adsabs.harvard.edu/abstract_service.html">NASA Astrophysics Data System (ADS)</a></p> <p>Sánchez, D.; Muñoz de Escalona, J. M.; Chacartegui, R.; Muñoz, A.; Sánchez, T.</p> <p></p> <p>A proposal for high efficiency hybrid systems based on molten carbonate fuel cells is presented in this paper. This proposal is based on adopting a closed cycle bottoming gas turbine using supercritical carbon dioxide as working fluid as opposed to open cycle hot air turbines typically used in this type of power generators. First, both bottoming cycles are compared for the same operating conditions, showing that their performances do not differ as much as initially expected, even if the initial objective of reducing compression work is accomplished satisfactorily. In view of these results, a profound review of research and industrial literature is carried out in order to determine realistic specifications for the principal components of the bottoming systems. From this analysis, it is concluded that an appropriate set of specifications must be developed for each bottoming cycle as the performances of compressor, turbine and recuperator differ significantly from one working fluid to another. Thus, when the operating conditions are updated, the performances of the resulting systems show a remarkable advantage of carbon dioxide based systems over conventional air units. Actually, the proposed hybrid system shows its capability to achieve 60% net efficiency, what represents a 10% increase with respect to the reference system.</p> </li> <li> <p><a target="_blank" rel="noopener noreferrer" onclick="trackOutboundLink('http://hdl.handle.net/2060/19960003385','NASA-TRS'); return false;" href="http://hdl.handle.net/2060/19960003385"><span>The role of tropical deforestation in the global carbon cycle: Spatial and temporal dynamics</span></a></p> <p><a target="_blank" rel="noopener noreferrer" href="http://ntrs.nasa.gov/search.jsp">NASA Technical Reports Server (NTRS)</a></p> <p>Houghton, R. A.; Skole, David; Moore, Berrien; Melillo, Jerry; Steudler, Paul</p> <p>1995-01-01</p> <p>'The Role of Tropical Deforestation in the Global Carbon cycle: Spatial and Temporal Dynamics', was a joint project involving the University of New Hampshire, the Marine Biological Laboratory, and the Woods Hole Research Center. The contribution of the Woods Hole Research Center consisted of three tasks: (1) assist University of New Hampshire in determining the net flux of carbon between the Brazilian Amazon and the atmosphere by means of a terrestrial carbon model; (2) address the spatial distribution of biomass across the Amazon Basin; and (3) assist NASA Headquarters in development of a science plan for the Terrestrial Ecology component of the NASA-Brazilian field campaign (anticipated for 1997-2001). Progress on these three tasks is briefly described.</p> </li> <li> <p><a target="_blank" rel="noopener noreferrer" onclick="trackOutboundLink('http://adsabs.harvard.edu/abs/2014AGUFM.B51J0133L','NASAADS'); return false;" href="http://adsabs.harvard.edu/abs/2014AGUFM.B51J0133L"><span>Carbonate concretions as a significant component of ancient marine carbon cycles: Insights from paired organic and inorganic carbon isotope analyses of a Cretaceous shale</span></a></p> <p><a target="_blank" rel="noopener noreferrer" href="http://adsabs.harvard.edu/abstract_service.html">NASA Astrophysics Data System (ADS)</a></p> <p>Loyd, S. J.</p> <p>2014-12-01</p> <p>Carbonate concretions often occur within fine-grained, organic-rich sedimentary rocks. This association reflects the common production of diagenetic minerals through biologic cycling of organic matter. Chemical analysis of carbonate concretions provides the rare opportunity to explore ancient shallow diagenetic environments, which are inherently transient due to progressive burial but are an integral component of the marine carbon cycle. The late Cretaceous Holz Shale (~80 Ma) contains abundant calcite concretions that exhibit textural and geochemical characteristics indicative of relatively shallow formation (i.e., near the sediment-water interface). Sampled concretions contain between 5.4 and 9.8 wt.% total inorganic carbon (TIC), or ~45 and 82 wt.% CaCO3, compared to host shale values which average ~1.5 wt.% TIC. Organic carbon isotope compositions (δ13Corg) are relatively constant in host and concretion samples ranging from -26.3 to -24.0‰ (VPDB). Carbonate carbon isotope compositions (δ13Ccarb) range from -22.5 to -3.4‰, indicating a significant but not entirely organic source of carbon. Concretions of the lower Holz Shale exhibit considerably elevated δ13Ccarb values averaging -4.8‰, whereas upper Holz Shale concretions express an average δ13Ccarb value of -17.0‰. If the remaining carbonate for lower Holz Shale concretions is sourced from marine fluids and/or dissolved marine carbonate minerals (e.g., shells), a simple mass balance indicates that ~28% of concretion carbon was sourced from organic matter and ~72% from late Cretaceous marine inorganic carbon (with δ13C ~ +2.5‰). Upper Holz Shale calculations indicate a ~73% contribution from organic matter and a ~27% contribution from inorganic carbon. When normalized for carbonate, organic contents within the concretions are ~2-13 wt.% enriched compared to host contents. This potentially reflects the protective nature of cementation that acts to limit permeability and chemical destruction of organic material. These data imply that concretion growth in shallow sediments can act as a significant and long-term sink for both marine inorganic and organic carbon.</p> </li> <li> <p><a target="_blank" rel="noopener noreferrer" onclick="trackOutboundLink('http://hdl.handle.net/2060/20120015581','NASA-TRS'); return false;" href="http://hdl.handle.net/2060/20120015581"><span>NASA's Carbon Monitoring System Flux-Pilot Project: A Multi-Component Analysis System for Carbon-Cycle Research and Monitoring</span></a></p> <p><a target="_blank" rel="noopener noreferrer" href="http://ntrs.nasa.gov/search.jsp">NASA Technical Reports Server (NTRS)</a></p> <p>Pawson, S.; Gunson, M.; Potter, C.; Jucks, K.</p> <p>2012-01-01</p> <p>The importance of greenhouse gas increases for climate motivates NASA s observing strategy for CO2 from space, including the forthcoming Orbiting Carbon Observatory (OCO-2) mission. Carbon cycle monitoring, including attribution of atmospheric concentrations to regional emissions and uptake, requires a robust modeling and analysis infrastructure to optimally extract information from the observations. NASA's Carbon-Monitoring System Flux-Pilot Project (FPP) is a prototype for such analysis, combining a set of unique tools to facilitate analysis of atmospheric CO2 along with fluxes between the atmosphere and the terrestrial biosphere or ocean. NASA's analysis system is unique, in that it combines information and expertise from the land, oceanic, and atmospheric branches of the carbon cycle and includes some estimates of uncertainty. Numerous existing space-based missions provide information of relevance to the carbon cycle. This study describes the components of the FPP framework, assessing the realism of computed fluxes, thus providing the basis for research and monitoring applications. Fluxes are computed using data-constrained terrestrial biosphere models and physical ocean models, driven by atmospheric observations and assimilating ocean-color information. Use of two estimates provides a measure of uncertainty in the fluxes. Along with inventories of other emissions, these data-derived fluxes are used in transport models to assess their consistency with atmospheric CO2 observations. Closure is achieved by using a four-dimensional data assimilation (inverse) approach that adjusts the terrestrial biosphere fluxes to make them consistent with the atmospheric CO2 observations. Results will be shown, illustrating the year-to-year variations in land biospheric and oceanic fluxes computed in the FPP. The signals of these surface-flux variations on atmospheric CO2 will be isolated using forward modeling tools, which also incorporate estimates of transport error. The results will be discussed in the context of interannual variability of observed atmospheric CO2 distributions.</p> </li> <li> <p><a target="_blank" rel="noopener noreferrer" onclick="trackOutboundLink('http://files.eric.ed.gov/fulltext/ED482726.pdf','ERIC'); return false;" href="http://files.eric.ed.gov/fulltext/ED482726.pdf"><span>Teaching and Learning about the Earth. ERIC Digest.</span></a></p> <p><a target="_blank" rel="noopener noreferrer" href="http://www.eric.ed.gov/ERICWebPortal/search/extended.jsp?_pageLabel=advanced">ERIC Educational Resources Information Center</a></p> <p>Lee, Hyonyong</p> <p></p> <p>This ERIC Digest investigates the earth and space science guidelines of the National Science Education Standards. These guidelines are frequently referred to as the earth system and include components such as plate tectonics, the water cycle, and the carbon cycle. This Digest describes the development of earth systems science and earth systems…</p> </li> <li> <p><a target="_blank" rel="noopener noreferrer" onclick="trackOutboundLink('https://www.fs.usda.gov/treesearch/pubs/53797','TREESEARCH'); return false;" href="https://www.fs.usda.gov/treesearch/pubs/53797"><span>Advancing the use of minirhizotrons in wetlands</span></a></p> <p><a target="_blank" rel="noopener noreferrer" href="http://www.fs.usda.gov/treesearch/">Treesearch</a></p> <p>C. M. Iversen; M. T. Murphy; M. F. Allen; J. Childs; D. M. Eissenstat; E.A. Lilleskov; T. M. Sarjala; V. L. Sloan; P. F. Sullivan</p> <p>2012-01-01</p> <p>Background. Wetlands store a substantial amount of carbon (C) in deep soil organic matter deposits, and play an important role in global fluxes of carbon dioxide and methane. Fine roots (i.e., ephemeral roots that are active in water and nutrient uptake) are recognized as important components of biogeochemical cycles in nutrient-limited wetland ecosystems. However,...</p> </li> <li> <p><a target="_blank" rel="noopener noreferrer" onclick="trackOutboundLink('http://www.ars.usda.gov/research/publications/publication/?seqNo115=326686','TEKTRAN'); return false;" href="http://www.ars.usda.gov/research/publications/publication/?seqNo115=326686"><span>Species identities, not functional groups, explain the effects of earthworms on litter carbon-derived soil respiration</span></a></p> <p><a target="_blank" rel="noopener noreferrer" href="https://www.ars.usda.gov/research/publications/find-a-publication/">USDA-ARS?s Scientific Manuscript database</a></p> <p></p> <p></p> <p>Soil respiration is frequently measured as a surrogate for biological activities and is important in soil carbon cycling. The heterotrophic component of soil respiration is primarily driven by microbial decomposition of leaf litter and soil organic matter, and is partially controlled by resource ava...</p> </li> <li> <p><a target="_blank" rel="noopener noreferrer" onclick="trackOutboundLink('https://www.fs.usda.gov/treesearch/pubs/43746','TREESEARCH'); return false;" href="https://www.fs.usda.gov/treesearch/pubs/43746"><span>Controls on winter ecosystem respiration in temperate and boreal ecosystems</span></a></p> <p><a target="_blank" rel="noopener noreferrer" href="http://www.fs.usda.gov/treesearch/">Treesearch</a></p> <p>T. Wang; P. Ciais; S.L. Piao; C. Ottle; P. Brender; F. Maignan; A. Arain; A. Cescatti; D. Gianelle; C. Gough; L Gu; P. Lafleur; T. Laurila; B. Marcolla; H. Margolis; L. Montagnani; E. Moors; N. Saigusa; T. Vesala; G. Wohlfahrt; C. Koven; A. Black; E. Dellwik; A. Don; D. Hollinger; A. Knohl; R. Monson; J. Munger; A. Suyker; A. Varlagin; S. Verma</p> <p>2011-01-01</p> <p>Winter CO2 fluxes represent an important component of the annual carbon budget in northern ecosystems. Understanding winter respiration processes and their responses to climate change is also central to our ability to assess terrestrial carbon cycle and climate feedbacks in the future. However, the factors influencing the spatial and temporal...</p> </li> <li> <p><a target="_blank" rel="noopener noreferrer" onclick="trackOutboundLink('https://www.ncbi.nlm.nih.gov/pubmed/27709910','PUBMED'); return false;" href="https://www.ncbi.nlm.nih.gov/pubmed/27709910"><span>Scenarios for Low Carbon and Low Water Electric Power Plant Operations: Implications for Upstream Water Use.</span></a></p> <p><a target="_blank" rel="noopener noreferrer" href="https://www.ncbi.nlm.nih.gov/entrez/query.fcgi?DB=pubmed">PubMed</a></p> <p>Dodder, Rebecca S; Barnwell, Jessica T; Yelverton, William H</p> <p>2016-11-01</p> <p>Electric sector water use, in particular for thermoelectric operations, is a critical component of the water-energy nexus. On a life cycle basis per unit of electricity generated, operational (e.g., cooling system) water use is substantially higher than water demands for the fuel cycle (e.g., natural gas and coal) and power plant manufacturing (e.g., equipment and construction). However, could shifting toward low carbon and low water electric power operations create trade-offs across the electricity life cycle? We compare business-as-usual with scenarios of carbon reductions and water constraints using the MARKet ALlocation (MARKAL) energy system model. Our scenarios show that, for water withdrawals, the trade-offs are minimal: operational water use accounts for over 95% of life cycle withdrawals. For water consumption, however, this analysis identifies potential trade-offs under some scenarios. Nationally, water use for the fuel cycle and power plant manufacturing can reach up to 26% of the total life cycle consumption. In the western United States, nonoperational consumption can even exceed operational demands. In particular, water use for biomass feedstock irrigation and manufacturing/construction of solar power facilities could increase with high deployment. As the United States moves toward lower carbon electric power operations, consideration of shifting water demands can help avoid unintended consequences.</p> </li> <li> <p><a target="_blank" rel="noopener noreferrer" onclick="trackOutboundLink('http://adsabs.harvard.edu/abs/1997AIPC..387.1227C','NASAADS'); return false;" href="http://adsabs.harvard.edu/abs/1997AIPC..387.1227C"><span>Carbon-carbon primary structure for SSTO vehicles</span></a></p> <p><a target="_blank" rel="noopener noreferrer" href="http://adsabs.harvard.edu/abstract_service.html">NASA Astrophysics Data System (ADS)</a></p> <p>Croop, Harold C.; Lowndes, Holland B.</p> <p>1997-01-01</p> <p>A hot structures development program is nearing completion to validate use of carbon-carbon composite structure for primary load carrying members in a single-stage-to-orbit, or SSTO, vehicle. A four phase program was pursued which involved design development and fabrication of a full-scale wing torque box demonstration component. The design development included vehicle and component selection, design criteria and approach, design data development, demonstration component design and analysis, test fixture design and analysis, demonstration component test planning, and high temperature test instrumentation development. The fabrication effort encompassed fabrication of structural elements for mechanical property verification as well as fabrication of the demonstration component itself and associated test fixturing. The demonstration component features 3D woven graphite preforms, integral spars, oxidation inhibited matrix, chemical vapor deposited (CVD) SiC oxidation protection coating, and ceramic matrix composite fasteners. The demonstration component has been delivered to the United States Air Force (USAF) for testing in the Wright Laboratory Structural Test Facility, WPAFB, OH. Multiple thermal-mechanical load cycles will be applied simulating two atmospheric cruise missions and one orbital mission. This paper discusses the overall approach to validation testing of the wing box component and presents some preliminary analytical test predictions.</p> </li> <li> <p><a target="_blank" rel="noopener noreferrer" onclick="trackOutboundLink('https://www.osti.gov/pages/biblio/1429606-molten-salt-power-towers-operating-salt-selection-cost-benefits','SCIGOV-DOEP'); return false;" href="https://www.osti.gov/pages/biblio/1429606-molten-salt-power-towers-operating-salt-selection-cost-benefits"><span>Molten salt power towers operating at 600–650 °C: Salt selection and cost benefits</span></a></p> <p><a target="_blank" rel="noopener noreferrer" href="http://www.osti.gov/pages">DOE PAGES</a></p> <p>Turchi, Craig S.; Vidal, Judith; Bauer, Matthew</p> <p>2018-03-14</p> <p>This analysis examines the potential benefit of adopting the supercritical carbon dioxide (sCO 2) Brayton cycle at 600-650 degrees C compared to the current state-of-the-art power tower operating a steam-Rankine cycle with solar salt at approximately 574 degrees C. The analysis compares a molten-salt power tower configuration using direct storage of solar salt (60:40 wt% sodium nitrate: potassium nitrate) or single-component nitrate salts at 600 degrees C or alternative carbonate- or chloride-based salts at 650 degrees C.</p> </li> <li> <p><a target="_blank" rel="noopener noreferrer" onclick="trackOutboundLink('https://www.osti.gov/biblio/1429606-molten-salt-power-towers-operating-salt-selection-cost-benefits','SCIGOV-STC'); return false;" href="https://www.osti.gov/biblio/1429606-molten-salt-power-towers-operating-salt-selection-cost-benefits"><span>Molten salt power towers operating at 600–650 °C: Salt selection and cost benefits</span></a></p> <p><a target="_blank" rel="noopener noreferrer" href="http://www.osti.gov/search">DOE Office of Scientific and Technical Information (OSTI.GOV)</a></p> <p>Turchi, Craig S.; Vidal, Judith; Bauer, Matthew</p> <p></p> <p>This analysis examines the potential benefit of adopting the supercritical carbon dioxide (sCO 2) Brayton cycle at 600-650 degrees C compared to the current state-of-the-art power tower operating a steam-Rankine cycle with solar salt at approximately 574 degrees C. The analysis compares a molten-salt power tower configuration using direct storage of solar salt (60:40 wt% sodium nitrate: potassium nitrate) or single-component nitrate salts at 600 degrees C or alternative carbonate- or chloride-based salts at 650 degrees C.</p> </li> <li> <p><a target="_blank" rel="noopener noreferrer" onclick="trackOutboundLink('http://adsabs.harvard.edu/abs/2017AGUFMOS24A..04D','NASAADS'); return false;" href="http://adsabs.harvard.edu/abs/2017AGUFMOS24A..04D"><span>Diagnosis of CO2 Fluxes in the Coastal Ocean</span></a></p> <p><a target="_blank" rel="noopener noreferrer" href="http://adsabs.harvard.edu/abstract_service.html">NASA Astrophysics Data System (ADS)</a></p> <p>Dai, M.; Cao, Z.; Yang, W.; Guo, X.; Yin, Z.; Zhao, Y.</p> <p>2017-12-01</p> <p>Coastal ocean carbon is an important component of the global carbon cycle. However, its mechanistic-based conceptualization, a prerequisite of coastal carbon modeling and its inclusion in the Earth System Model, remains difficult due to the highest variability in both time and space. Here we show that the inter-seasonal change of the global coastal pCO2 is more determined by non-temperature factors such as biological drawdown and water mass mixing, the latter of which features the dynamic boundary processes of the coastal ocean at both land-margin and margin-open ocean interfaces. Considering these unique features, we resolve the coastal CO2 fluxes using a semi-analytical approach coupling physics-biogeochemistry and carbon-nutrients and conceptualize the coastal carbon cycle into Ocean-dominated Margins (OceMar) and River-dominated Ocean Margins (RiOMar). The diagnostic result of CO2 fluxes in the South China Sea basin and the Arabian Sea as OceMars and in the Pearl River Plume as a RioMar is consistent with field observations. Our mechanistic-based diagnostic approach therefore helps better understand and model coastal carbon cycle yet the stoichiometry of carbon-nutrients coupling needs scrutiny when applying our approach.</p> </li> <li> <p><a target="_blank" rel="noopener noreferrer" onclick="trackOutboundLink('http://adsabs.harvard.edu/abs/2016AGUOS.B34B0361S','NASAADS'); return false;" href="http://adsabs.harvard.edu/abs/2016AGUOS.B34B0361S"><span>Implications of a More Comprehensive Nitrogen Cycle in a Global Biogeochemical Ocean Model</span></a></p> <p><a target="_blank" rel="noopener noreferrer" href="http://adsabs.harvard.edu/abstract_service.html">NASA Astrophysics Data System (ADS)</a></p> <p>Six, K. D.; Ilyina, T.</p> <p>2016-02-01</p> <p>Nitrogen plays a crucial role for nearly all living organisms in the Earth system. Changes in the marine nitrogen cycle not only alter the marine biota, but will also have an impact on the marine carbon cycle and, in turn, on climate due to the close coupling of the carbon-nitrogen cycle. The understanding of processes and controls of the marine nitrogen cycle is therefore a prerequisite to reduce uncertainties in the prediction of future climate. Nevertheless, most ocean biogeochemical components of modern Earth system models have a rather simplistic representation of marine N-cycle mainly focusing on nitrate. Here we present results of the HAMburg Ocean Carbon Cycle model (HAMOCC) as part of the MPI-ESM which was extended by a prognostic representation of ammonium and nitrite to resolve important processes of the marine N-cycle such as nitrification and anaerobic ammonium oxidation (anammox). Additionally, we updated the production of nitrous oxide, an important greenhouse gas, allowing for two sources from oxidation of ammonium (nitrification) and from reduction of nitrite (nitrifier-denitrification) at low oxygen concentrations. Besides an extended model data comparison we discuss the following aspects of the N-cycle by model means: (1) contribution of anammox to the loss of fixed nitrogen, and (2) production and emission of marine nitrous oxide.</p> </li> <li> <p><a target="_blank" rel="noopener noreferrer" onclick="trackOutboundLink('https://www.fs.usda.gov/treesearch/pubs/30703','TREESEARCH'); return false;" href="https://www.fs.usda.gov/treesearch/pubs/30703"><span>Nondestructive system for analyzing carbon in the soil</span></a></p> <p><a target="_blank" rel="noopener noreferrer" href="http://www.fs.usda.gov/treesearch/">Treesearch</a></p> <p>Lucian Wielopolski; George Hendrey; Kurt H. Johnsen; Sudeep Mitra; Stephen A. Prior; Huga H. Rogers; H. Allen Torbert</p> <p>2008-01-01</p> <p>Carbon is an essential component of life and, in its organic form, plays a pivotal role in the soilâs fertility, productivity, and water retention. It is an integral part of the atmosphericâterrestrial C exchange cycle mediated via photosynthesis; furthermore, it emerged recently as a new trading commodity, i.e., âcarbon credits.â When carefully manipulated, C...</p> </li> <li> <p><a target="_blank" rel="noopener noreferrer" onclick="trackOutboundLink('https://www.fs.usda.gov/treesearch/pubs/50987','TREESEARCH'); return false;" href="https://www.fs.usda.gov/treesearch/pubs/50987"><span>A watershed-scale characterication of dissolved organic carbon and nutrients on the South Carolina Coastal Plain</span></a></p> <p><a target="_blank" rel="noopener noreferrer" href="http://www.fs.usda.gov/treesearch/">Treesearch</a></p> <p>Daniel L. Tufford; Setsen Alton-Ochir; Warren Hankinson</p> <p>2016-01-01</p> <p>Dissolved organic matter (DOM) is recognized as a major component in the global carbon cycle and is an important driver of numerous biogeochemical processes in aquatic ecosystems, both in-stream and downstream in estuaries. This study sought to characterize chromophoric DOM (CDOM), dissolved organic carbon (DOC), and dissolved nutrients in major rivers and their...</p> </li> <li> <p><a target="_blank" rel="noopener noreferrer" onclick="trackOutboundLink('https://www.fs.usda.gov/treesearch/pubs/50889','TREESEARCH'); return false;" href="https://www.fs.usda.gov/treesearch/pubs/50889"><span>A watershed-scale characterization of dissolved organic carbon and nutrients on the South Carolina Coastal Plain</span></a></p> <p><a target="_blank" rel="noopener noreferrer" href="http://www.fs.usda.gov/treesearch/">Treesearch</a></p> <p>Daniel Tufford; Setsen Alton-Ochir</p> <p>2016-01-01</p> <p>Dissolved organic matter (DOM) is recognized as a major component in the global carbon cycle and is an important driver of numerous biogeochemical processes in aquatic ecosystems, both in-stream and downstream in estuaries. This study sought to characterize chromophoric DOM (CDOM), dissolved organic carbon (DOC), and dissolved nutrients in major rivers and their...</p> </li> </ol> <div class="pull-right"> <ul class="pagination"> <li><a href="#" onclick='return showDiv("page_1");'>«</a></li> <li><a href="#" onclick='return showDiv("page_2");'>2</a></li> <li><a href="#" onclick='return showDiv("page_3");'>3</a></li> <li class="active"><span>4</span></li> <li><a href="#" onclick='return showDiv("page_5");'>5</a></li> <li><a href="#" onclick='return showDiv("page_6");'>6</a></li> <li><a href="#" onclick='return showDiv("page_25");'>»</a></li> </ul> </div> </div><!-- col-sm-12 --> </div><!-- row --> </div><!-- page_4 --> <div id="page_5" class="hiddenDiv"> <div class="row"> <div class="col-sm-12"> <div class="pull-right"> <ul class="pagination"> <li><a href="#" onclick='return showDiv("page_1");'>«</a></li> <li><a href="#" onclick='return showDiv("page_3");'>3</a></li> <li><a href="#" onclick='return showDiv("page_4");'>4</a></li> <li class="active"><span>5</span></li> <li><a href="#" onclick='return showDiv("page_6");'>6</a></li> <li><a href="#" onclick='return showDiv("page_7");'>7</a></li> <li><a href="#" onclick='return showDiv("page_25");'>»</a></li> </ul> </div> </div> </div> <div class="row"> <div class="col-sm-12"> <ol class="result-class" start="81"> <li> <p><a target="_blank" rel="noopener noreferrer" onclick="trackOutboundLink('https://pubs.er.usgs.gov/publication/70159437','USGSPUBS'); return false;" href="https://pubs.er.usgs.gov/publication/70159437"><span>Component-specific dynamics of riverine mangrove CO2 efflux in the Florida coastal Everglades</span></a></p> <p><a target="_blank" rel="noopener noreferrer" href="http://pubs.er.usgs.gov/pubs/index.jsp?view=adv">USGS Publications Warehouse</a></p> <p>Troxler, Tiffany G.; Barr, Jordan G.; Fuentes, Jose D.; Engel, Victor C.; Anderson, Gordon H.; Sanchez, Christopher; Lagomosino, David; Price, Rene; Davis, Stephen E.</p> <p>2015-01-01</p> <p>Carbon cycling in mangrove forests represents a significant portion of the coastal wetland carbon (C) budget across the latitudes of the tropics and subtropics. Previous research suggests fluctuations in tidal inundation, temperature and salinity can influence forest metabolism and C cycling. Carbon dioxide (CO2) from respiration that occurs from below the canopy is contributed from different components. In this study, we investigated variation in CO2 flux among different below-canopy components (soil, leaf litter, course woody debris, soil including pneumatophores, prop roots, and surface water) in a riverine mangrove forest of Shark River Slough estuary, Everglades National Park (Florida, USA). The range in CO2 flux from different components exceeded that measured among sites along the oligohaline-saline gradient. Black mangrove (Avicennia germinans) pneumatophores contributed the largest average CO2 flux. Over a narrow range of estuarine salinity (25–35 practical salinity units (PSU)), increased salinity resulted in lower CO2 flux to the atmosphere. Tidal inundation reduced soil CO2 flux overall but increased the partial pressure of CO2 (pCO2) observed in the overlying surface water upon flooding. Higher pCO2 in surface water is then subject to tidally driven export, largely as HCO3. Integration and scaling of CO2 flux rates to forest scale allowed for improved understanding of the relative contribution of different below-canopy components to mangrove forest ecosystem respiration (ER). Summing component CO2fluxes suggests a more significant contribution of below-canopy respiration to ER than previously considered. An understanding of below-canopy CO2 component fluxes and their contributions to ER can help to elucidate how C cycling will change with discrete disturbance events (e.g., hurricanes) and long-term change, including sea-level rise, and potential impact mangrove forests. As such, key controls on below-canopy ER must be taken into consideration when developing and modeling mangrove forest C budgets.</p> </li> <li> <p><a target="_blank" rel="noopener noreferrer" onclick="trackOutboundLink('https://www.osti.gov/servlets/purl/1425642','SCIGOV-STC'); return false;" href="https://www.osti.gov/servlets/purl/1425642"><span>Microbial potential for carbon and nutrient cycling in a geogenic supercritical carbon dioxide reservoir: Microbial life in the deep carbonated biosphere</span></a></p> <p><a target="_blank" rel="noopener noreferrer" href="http://www.osti.gov/search">DOE Office of Scientific and Technical Information (OSTI.GOV)</a></p> <p>Freedman, Adam J. E.; Tan, BoonFei; Thompson, Janelle R.</p> <p></p> <p>Microorganisms catalyze carbon cycling and biogeochemical reactions in the deep subsurface and thus may be expected to influence the fate of injected super-critical (sc) CO 2 following geological carbon sequestration (GCS). We hypothesized that natural subsurface scCO 2 reservoirs, which serve as analogs for the long-term fate of sequestered scCO 2 harbor a ‘deep carbonated biosphere’ with carbon cycling potential. We sampled subsurface fluids from scCO 2- water separators at a natural scCO 2 reservoir at McElmo Dome, Colorado for analysis of 16S rRNA gene diversity and metagenome content. Sequence annotations indicated dominance of Sulfurospirillum, Rhizobium, Desulfovibrio and four membersmore » of the Clostridiales family. Genomes extracted from metagenomes using homology and compositional approaches revealed diverse mechanisms for growth and nutrient cycling, including pathways for CO 2 and N 2 fixation, anaerobic respiration, sulfur oxidation, fermentation and potential for metabolic syntrophy. Differences in biogeochemical potential between two production well communities were consistent with differences in fluid chemical profiles, suggesting a potential link between microbial activity and geochemistry. In conclusion, the existence of a microbial ecosystem associated with the McElmo Dome scCO 2 reservoir indicates that potential impacts of the deep biosphere on CO 2 fate and transport should be taken into consideration as a component of GCS planning and modelling.« less</p> </li> <li> <p><a target="_blank" rel="noopener noreferrer" onclick="trackOutboundLink('https://www.osti.gov/pages/biblio/1425642-microbial-potential-carbon-nutrient-cycling-geogenic-supercritical-carbon-dioxide-reservoir-microbial-life-deep-carbonated-biosphere','SCIGOV-DOEP'); return false;" href="https://www.osti.gov/pages/biblio/1425642-microbial-potential-carbon-nutrient-cycling-geogenic-supercritical-carbon-dioxide-reservoir-microbial-life-deep-carbonated-biosphere"><span>Microbial potential for carbon and nutrient cycling in a geogenic supercritical carbon dioxide reservoir: Microbial life in the deep carbonated biosphere</span></a></p> <p><a target="_blank" rel="noopener noreferrer" href="http://www.osti.gov/pages">DOE PAGES</a></p> <p>Freedman, Adam J. E.; Tan, BoonFei; Thompson, Janelle R.</p> <p>2017-05-02</p> <p>Microorganisms catalyze carbon cycling and biogeochemical reactions in the deep subsurface and thus may be expected to influence the fate of injected super-critical (sc) CO 2 following geological carbon sequestration (GCS). We hypothesized that natural subsurface scCO 2 reservoirs, which serve as analogs for the long-term fate of sequestered scCO 2 harbor a ‘deep carbonated biosphere’ with carbon cycling potential. We sampled subsurface fluids from scCO 2- water separators at a natural scCO 2 reservoir at McElmo Dome, Colorado for analysis of 16S rRNA gene diversity and metagenome content. Sequence annotations indicated dominance of Sulfurospirillum, Rhizobium, Desulfovibrio and four membersmore » of the Clostridiales family. Genomes extracted from metagenomes using homology and compositional approaches revealed diverse mechanisms for growth and nutrient cycling, including pathways for CO 2 and N 2 fixation, anaerobic respiration, sulfur oxidation, fermentation and potential for metabolic syntrophy. Differences in biogeochemical potential between two production well communities were consistent with differences in fluid chemical profiles, suggesting a potential link between microbial activity and geochemistry. In conclusion, the existence of a microbial ecosystem associated with the McElmo Dome scCO 2 reservoir indicates that potential impacts of the deep biosphere on CO 2 fate and transport should be taken into consideration as a component of GCS planning and modelling.« less</p> </li> <li> <p><a target="_blank" rel="noopener noreferrer" onclick="trackOutboundLink('http://adsabs.harvard.edu/abs/2016EGUGA..18.9277E','NASAADS'); return false;" href="http://adsabs.harvard.edu/abs/2016EGUGA..18.9277E"><span>Monitoring and Predicting the Export and Fate of Global Ocean Net Primary Production: The EXPORTS Field Program</span></a></p> <p><a target="_blank" rel="noopener noreferrer" href="http://adsabs.harvard.edu/abstract_service.html">NASA Astrophysics Data System (ADS)</a></p> <p>Exports Science Definition Team</p> <p>2016-04-01</p> <p>Ocean ecosystems play a critical role in the Earth's carbon cycle and its quantification on global scales remains one of the greatest challenges in global ocean biogeochemistry. The goal of the EXport Processes in the Ocean from Remote Sensing (EXPORTS) science plan is to develop a predictive understanding of the export and fate of global ocean primary production and its implications for the Earth's carbon cycle in present and future climates. NASA's satellite ocean-color data record has revolutionized our understanding of global marine systems. EXPORTS is designed to advance the utility of NASA ocean color assets to predict how changes in ocean primary production will impact the global carbon cycle. EXPORTS will create a predictive understanding of both the export of organic carbon from the euphotic zone and its fate in the underlying "twilight zone" (depths of 500 m or more) where variable fractions of exported organic carbon are respired back to CO2. Ultimately, it is the sequestration of deep organic carbon transport that defines the impact of ocean biota on atmospheric CO2 levels and hence climate. EXPORTS will generate a new, detailed understanding of ocean carbon transport processes and pathways linking upper ocean phytoplankton processes to the export and fate of organic matter in the underlying twilight zone using a combination of field campaigns, remote sensing and numerical modeling. The overarching objective for EXPORTS is to ensure the success of future satellite missions by establishing mechanistic relationships between remotely sensed signals and carbon cycle processes. Through a process-oriented approach, EXPORTS will foster new insights on ocean carbon cycling that will maximize its societal relevance and be a key component in the U.S. investment to understand Earth as an integrated system.</p> </li> <li> <p><a target="_blank" rel="noopener noreferrer" onclick="trackOutboundLink('https://www.ncbi.nlm.nih.gov/pubmed/29433047','PUBMED'); return false;" href="https://www.ncbi.nlm.nih.gov/pubmed/29433047"><span>Effect of tricarboxylic acid cycle regulator on carbon retention and organic component transformation during food waste composting.</span></a></p> <p><a target="_blank" rel="noopener noreferrer" href="https://www.ncbi.nlm.nih.gov/entrez/query.fcgi?DB=pubmed">PubMed</a></p> <p>Lu, Qian; Zhao, Yue; Gao, Xintong; Wu, Junqiu; Zhou, Haixuan; Tang, Pengfei; Wei, Qingbin; Wei, Zimin</p> <p>2018-05-01</p> <p>Composting is an environment friendly method to recycling organic waste. However, with the increasing concern about greenhouse gases generated in global atmosphere, it is significant to reduce the emission of carbon dioxide (CO 2 ). This study analyzes tricarboxylic acid (TCA) cycle regulators on the effect of reducing CO 2 emission, and the relationship among organic component (OC) degradation and transformation and microorganism during composting. The results showed that adding adenosine tri-phosphate (ATP) and nicotinamide adenine dinucleotide (NADH) could enhance the transformation of OC and increase the diversity of microorganism community. Malonic acid (MA) as a competitive inhibitor could decrease the emission of CO 2 by inhibiting the TCA cycle. A structural equation model was established to explore effects of different OC and microorganism on humic acid (HA) concentration during composting. Furthermore, added MA provided an environmental benefit in reducing the greenhouse gas emission for manufacture sustainable products. Copyright © 2018 Elsevier Ltd. All rights reserved.</p> </li> <li> <p><a target="_blank" rel="noopener noreferrer" onclick="trackOutboundLink('http://adsabs.harvard.edu/abs/2016EGUGA..18.1020H','NASAADS'); return false;" href="http://adsabs.harvard.edu/abs/2016EGUGA..18.1020H"><span>The biological carbon pump in the ocean: Reviewing model representations and its feedbacks on climate perturbations.</span></a></p> <p><a target="_blank" rel="noopener noreferrer" href="http://adsabs.harvard.edu/abstract_service.html">NASA Astrophysics Data System (ADS)</a></p> <p>Hülse, Dominik; Arndt, Sandra; Ridgwell, Andy; Wilson, Jamie</p> <p>2016-04-01</p> <p>The ocean-sediment system, as the biggest carbon reservoir in the Earth's carbon cycle, plays a crucial role in regulating atmospheric carbon dioxide concentrations and climate. Therefore, it is essential to constrain the importance of marine carbon cycle feedbacks on global warming and ocean acidification. Arguably, the most important single component of the ocean's carbon cycle is the so-called "biological carbon pump". It transports carbon that is fixed in the light-flooded surface layer of the ocean to the deep ocean and the surface sediment, where it is degraded/dissolved or finally buried in the deep sediments. Over the past decade, progress has been made in understanding different factors that control the efficiency of the biological carbon pump and their feedbacks on the global carbon cycle and climate (i.e. ballasting = ocean acidification feedback; temperature dependant organic matter degradation = global warming feedback; organic matter sulphurisation = anoxia/euxinia feedback). Nevertheless, many uncertainties concerning the interplay of these processes and/or their relative significance remain. In addition, current Earth System Models tend to employ empirical and static parameterisations of the biological pump. As these parametric representations are derived from a limited set of present-day observations, their ability to represent carbon cycle feedbacks under changing climate conditions is limited. The aim of my research is to combine past carbon cycling information with a spatially resolved global biogeochemical model to constrain the functioning of the biological pump and to base its mathematical representation on a more mechanistic approach. Here, I will discuss important aspects that control the efficiency of the ocean's biological carbon pump, review how these processes of first order importance are mathematically represented in existing Earth system Models of Intermediate Complexity (EMIC) and distinguish different approaches to approximate biogeochemical processes in the sediments. The performance of the respective mathematical representations in constraining the importance of carbon pump feedbacks on marine biogeochemical dynamics is then compared and evaluated under different extreme climate scenarios (e.g. OAE2, Eocene) using the Earth system model 'GENIE' and proxy records. The compiled mathematical descriptions and the model results underline the lack of a complete and mechanistic framework to represent the short-term carbon cycle in most EMICs which seriously limits the ability of these models to constrain the response of the ocean's carbon cycle to past and in particular future climate change. In conclusion, this presentation will critically evaluate the approaches currently used in marine biogeochemical modelling and outline key research directions concerning model development in the future.</p> </li> <li> <p><a target="_blank" rel="noopener noreferrer" onclick="trackOutboundLink('https://www.osti.gov/servlets/purl/1254576','SCIGOV-STC'); return false;" href="https://www.osti.gov/servlets/purl/1254576"><span>Deciphering ocean carbon in a changing world</span></a></p> <p><a target="_blank" rel="noopener noreferrer" href="http://www.osti.gov/search">DOE Office of Scientific and Technical Information (OSTI.GOV)</a></p> <p>Moran, Mary Ann; Kujawinski, Elizabeth B.; Stubbins, Aron</p> <p></p> <p>Dissolved organic matter (DOM) in the oceans is one of the largest pools of reduced carbon on Earth, comparable in size to the atmospheric CO 2 reservoir. The cycling of DOM over short and long time scales has profound impacts on the quantity of carbon sequestered in the oceans and the foundations of the food webs that support ocean life. At the heart of this cycle lie molecular-level relationships between the individual molecules in DOM and the members of the ocean microbiome that produce and consume them. In the past, these connections have defied clear definition and study because bothmore » DOM and microbial communities consist of many thousands of individual components. Emerging tools in analytical chemistry, microbiology and informatics are breaking down the barriers to a fuller appreciation of these connections. Furthermore, we highlight questions that are being addressed using this new toolkit and consider how these advances are transforming our understanding of some of the most important reactions of the marine carbon cycle.« less</p> </li> <li> <p><a target="_blank" rel="noopener noreferrer" onclick="trackOutboundLink('https://www.osti.gov/biblio/1254576-deciphering-ocean-carbon-changing-world','SCIGOV-STC'); return false;" href="https://www.osti.gov/biblio/1254576-deciphering-ocean-carbon-changing-world"><span>Deciphering ocean carbon in a changing world</span></a></p> <p><a target="_blank" rel="noopener noreferrer" href="http://www.osti.gov/search">DOE Office of Scientific and Technical Information (OSTI.GOV)</a></p> <p>Moran, Mary Ann; Kujawinski, Elizabeth B.; Stubbins, Aron</p> <p>2016-03-07</p> <p>Dissolved organic matter (DOM) in the oceans is one of the largest pools of reduced carbon on Earth, comparable in size to the atmospheric CO2 reservoir. The cycling of DOM over short and long time scales has profound impacts on the quantity of carbon sequestered in the oceans and the foundations of the food webs that support ocean life. At the heart of this cycle lie molecular-level relationships between the individual molecules in DOM and the members of the ocean microbiome that produce and consume them. In the past, these connections have defied clear definition and study because both DOMmore » and microbial communities consist of many thousands of individual components. Emerging tools in analytical chemistry, microbiology and informatics are breaking down the barriers to a fuller appreciation of these connections. Here we highlight questions that are being addressed using this new toolkit and consider how these advances are transforming our understanding of some of the most important reactions of the marine carbon cycle.« less</p> </li> <li> <p><a target="_blank" rel="noopener noreferrer" onclick="trackOutboundLink('https://www.osti.gov/pages/biblio/1254576-deciphering-ocean-carbon-changing-world','SCIGOV-DOEP'); return false;" href="https://www.osti.gov/pages/biblio/1254576-deciphering-ocean-carbon-changing-world"><span>Deciphering ocean carbon in a changing world</span></a></p> <p><a target="_blank" rel="noopener noreferrer" href="http://www.osti.gov/pages">DOE PAGES</a></p> <p>Moran, Mary Ann; Kujawinski, Elizabeth B.; Stubbins, Aron; ...</p> <p>2016-03-07</p> <p>Dissolved organic matter (DOM) in the oceans is one of the largest pools of reduced carbon on Earth, comparable in size to the atmospheric CO 2 reservoir. The cycling of DOM over short and long time scales has profound impacts on the quantity of carbon sequestered in the oceans and the foundations of the food webs that support ocean life. At the heart of this cycle lie molecular-level relationships between the individual molecules in DOM and the members of the ocean microbiome that produce and consume them. In the past, these connections have defied clear definition and study because bothmore » DOM and microbial communities consist of many thousands of individual components. Emerging tools in analytical chemistry, microbiology and informatics are breaking down the barriers to a fuller appreciation of these connections. Furthermore, we highlight questions that are being addressed using this new toolkit and consider how these advances are transforming our understanding of some of the most important reactions of the marine carbon cycle.« less</p> </li> <li> <p><a target="_blank" rel="noopener noreferrer" onclick="trackOutboundLink('http://adsabs.harvard.edu/abs/2017E%26PSL.479..241B','NASAADS'); return false;" href="http://adsabs.harvard.edu/abs/2017E%26PSL.479..241B"><span>Testing Urey's carbonate-silicate cycle using the calcium isotopic composition of sedimentary carbonates</span></a></p> <p><a target="_blank" rel="noopener noreferrer" href="http://adsabs.harvard.edu/abstract_service.html">NASA Astrophysics Data System (ADS)</a></p> <p>Blättler, Clara L.; Higgins, John A.</p> <p>2017-12-01</p> <p>Carbonate minerals constitute a major component of the sedimentary geological record and an archive of a fraction of the carbon and calcium cycled through the Earth's surface reservoirs for over three billion years. For calcium, carbonate minerals constitute the ultimate sink for almost all calcium liberated during continental and submarine weathering of silicate minerals. This study presents >500 stable isotope ratios of calcium in Precambrian carbonate sediments, both limestones and dolomites, in an attempt to characterize the isotope mass balance of the sedimentary carbonate reservoir through time. The mean of the dataset is indistinguishable from estimates of the calcium isotope ratio of bulk silicate Earth, consistent with the Urey cycle being the dominant mechanism exchanging calcium among surface reservoirs. The variability in bulk sediment calcium isotope ratios within each geological unit does not reflect changes in the global calcium cycle, but rather highlights the importance of local mineralogical and/or diagenetic effects in the carbonate record. This dataset demonstrates the potential for calcium isotope ratios to help assess these local effects, such as the former presence of aragonite, even in rocks with a history of neomorphism and recrystallization. Additionally, 29 calcium isotope measurements are presented from ODP (Ocean Drilling Program) Site 801 that contribute to the characterization of altered oceanic crust as an additional sink for calcium, and whose distinct isotopic signature places a limit on the importance of this subduction flux over Earth history.</p> </li> <li> <p><a target="_blank" rel="noopener noreferrer" onclick="trackOutboundLink('http://www.ars.usda.gov/research/publications/publication/?seqNo115=294248','TEKTRAN'); return false;" href="http://www.ars.usda.gov/research/publications/publication/?seqNo115=294248"><span>Can current moisture responses predict soil CO2 efflux under altered precipitation regimes? A synthesis of manipulation experiments</span></a></p> <p><a target="_blank" rel="noopener noreferrer" href="https://www.ars.usda.gov/research/publications/find-a-publication/">USDA-ARS?s Scientific Manuscript database</a></p> <p></p> <p></p> <p>As a key component of the carbon cycle, soil respiration (Rsoil) is being excessively studied with the aim of improving our understanding as well as our ability to predict Rsoil when climate changes. Many manipulation experiments have been performed to test how Rsoil and other carbon fluxes and ecos...</p> </li> <li> <p><a target="_blank" rel="noopener noreferrer" onclick="trackOutboundLink('https://www.fs.usda.gov/treesearch/pubs/34850','TREESEARCH'); return false;" href="https://www.fs.usda.gov/treesearch/pubs/34850"><span>Harvest impacts on soil carbon storage in temperate forests</span></a></p> <p><a target="_blank" rel="noopener noreferrer" href="http://www.fs.usda.gov/treesearch/">Treesearch</a></p> <p>L.E. Nave; E.D. Vance; C.W. Swanston; P.S. Curtis</p> <p>2010-01-01</p> <p>Forest soil carbon (C) storage is a significant component of the global C cycle, and is important for sustaining forest productivity. Although forest management may have substantial impacts on soil C storage, experimental data from forest harvesting studies have not been synthesized recently. To quantify the effects of harvesting on soil C, and to identify sources of...</p> </li> <li> <p><a target="_blank" rel="noopener noreferrer" onclick="trackOutboundLink('https://www.fs.usda.gov/treesearch/pubs/5212','TREESEARCH'); return false;" href="https://www.fs.usda.gov/treesearch/pubs/5212"><span>Carbon Cycling in Wetland Forest Soils</span></a></p> <p><a target="_blank" rel="noopener noreferrer" href="http://www.fs.usda.gov/treesearch/">Treesearch</a></p> <p>Carl C. Trettin; Martin F. Jurgensen</p> <p>2003-01-01</p> <p>Wetlands comprise a small proportion (i.e., 2 to 3%) of earth's terrestrial surface, yet they contain a significant proportion of the terrestrial carbon (C) pool. Soils comprise the largest terrestrial C pool (ca. 1550 Pg C in upper 100 cm; Eswaran et al., 1993; Batjes, 1996), and wetlands contain the single largest component, with estimates ranging between 18...</p> </li> <li> <p><a target="_blank" rel="noopener noreferrer" onclick="trackOutboundLink('http://adsabs.harvard.edu/abs/2017AGUFMGC21C0958L','NASAADS'); return false;" href="http://adsabs.harvard.edu/abs/2017AGUFMGC21C0958L"><span>Impact of a regional drought on terrestrial carbon fluxes and atmospheric carbon: results from a coupled carbon cycle model</span></a></p> <p><a target="_blank" rel="noopener noreferrer" href="http://adsabs.harvard.edu/abstract_service.html">NASA Astrophysics Data System (ADS)</a></p> <p>Lee, E.; Koster, R. D.; Ott, L. E.; Weir, B.; Mahanama, S. P. P.; Chang, Y.; Zeng, F.</p> <p>2017-12-01</p> <p>Understanding the underlying processes that control the carbon cycle is key to predicting future global change. Much of the uncertainty in the magnitude and variability of the atmospheric carbon dioxide (CO2) stems from uncertainty in terrestrial carbon fluxes. Budget-based analyses show that such fluxes exhibit substantial interannual variability, but the relative impacts of temperature and moisture variations on regional and global scales are poorly understood. Here we investigate the impact of a regional drought on terrestrial carbon fluxes and CO2 mixing ratios over North America using the NASA Goddard Earth Observing System (GEOS) Model. Two 48-member ensembles of NASA GEOS-5 simulations with fully coupled land and atmosphere carbon components are performed - a control ensemble and an ensemble with an artificially imposed dry land surface anomaly for three months (April-June) over the lower Mississippi River Valley. Comparison of the results using the ensemble approach allows a direct quantification of the impact of the regional drought on local and proximate carbon exchange at the land surface via the carbon-water feedback processes.</p> </li> <li> <p><a target="_blank" rel="noopener noreferrer" onclick="trackOutboundLink('http://adsabs.harvard.edu/abs/2012EGUGA..14.8151M','NASAADS'); return false;" href="http://adsabs.harvard.edu/abs/2012EGUGA..14.8151M"><span>Simulating forest productivity along a neotropical elevational transect: temperature variation and carbon use efficiency</span></a></p> <p><a target="_blank" rel="noopener noreferrer" href="http://adsabs.harvard.edu/abstract_service.html">NASA Astrophysics Data System (ADS)</a></p> <p>Marthews, T.; Malhi, Y.; Girardin, C.; Silva-Espejo, J.; Aragão, L.; Metcalfe, D.; Rapp, J.; Mercado, L.; Fisher, R.; Galbraith, D.; Fisher, J.; Salinas-Revilla, N.; Friend, A.; Restrepo-Coupe, N.; Williams, R.</p> <p>2012-04-01</p> <p>A better understanding of the mechanisms controlling the magnitude and sign of carbon components in tropical forest ecosystems is important for reliable estimation of this important regional component of the global carbon cycle. We used the JULES vegetation model to simulate all components of the carbon balance at six sites along an Andes-Amazon transect across Peru and Brazil and compared the results to published field measurements. In the upper montane zone the model predicted a vegetation dieback, indicating a need for better parameterisation of cloud forest vegetation. In the lower montane and lowland zones simulated ecosystem productivity and respiration were predicted with reasonable accuracy, although not always within the error bounds of the observations. Model-predicted carbon use efficiency in this transect surprisingly did not increase with elevation, but remained close to the 'temperate' value 0.5. This may be explained by elevational changes in the balance between growth and maintenance respiration within the forest canopy, as controlled by both temperature- and pressure-mediated processes.</p> </li> <li> <p><a target="_blank" rel="noopener noreferrer" onclick="trackOutboundLink('http://adsabs.harvard.edu/abs/2016EGUGA..18.9001F','NASAADS'); return false;" href="http://adsabs.harvard.edu/abs/2016EGUGA..18.9001F"><span>A mechanistic soil biogeochemistry model with explicit representation of microbial and macrofaunal activities and nutrient cycles</span></a></p> <p><a target="_blank" rel="noopener noreferrer" href="http://adsabs.harvard.edu/abstract_service.html">NASA Astrophysics Data System (ADS)</a></p> <p>Fatichi, Simone; Manzoni, Stefano; Or, Dani; Paschalis, Athanasios</p> <p>2016-04-01</p> <p>The potential of a given ecosystem to store and release carbon is inherently linked to soil biogeochemical processes. These processes are deeply connected to the water, energy, and vegetation dynamics above and belowground. Recently, it has been advocated that a mechanistic representation of soil biogeochemistry require: (i) partitioning of soil organic carbon (SOC) pools according to their functional role; (ii) an explicit representation of microbial dynamics; (iii) coupling of carbon and nutrient cycles. While some of these components have been introduced in specialized models, they have been rarely implemented in terrestrial biosphere models and tested in real cases. In this study, we combine a new soil biogeochemistry model with an existing model of land-surface hydrology and vegetation dynamics (T&C). Specifically the soil biogeochemistry component explicitly separates different litter pools and distinguishes SOC in particulate, dissolved and mineral associated fractions. Extracellular enzymes and microbial pools are explicitly represented differentiating the functional roles of bacteria, saprotrophic and mycorrhizal fungi. Microbial activity depends on temperature, soil moisture and litter or SOC stoichiometry. The activity of macrofauna is also modeled. Nutrient dynamics include the cycles of nitrogen, phosphorous and potassium. The model accounts for feedbacks between nutrient limitations and plant growth as well as for plant stoichiometric flexibility. In turn, litter input is a function of the simulated vegetation dynamics. Root exudation and export to mycorrhiza are computed based on a nutrient uptake cost function. The combined model is tested to reproduce respiration dynamics and nitrogen cycle in few sites where data were available to test plausibility of results across a range of different metrics. For instance in a Swiss grassland ecosystem, fine root, bacteria, fungal and macrofaunal respiration account for 40%, 23%, 33% and 4% of total belowground respiration, respectively. Root exudation and carbon export to mycorrhizal represent about 7% of plant Net Primary Production. The model allows exploring the temporal dynamics of respiration fluxes from the different ecosystem components and designing virtual experiments on the controls exerted by environmental variables and/or soil microbes and mycorrhizal associations on soil carbon storage, plant growth, and nutrient leaching.</p> </li> <li> <p><a target="_blank" rel="noopener noreferrer" onclick="trackOutboundLink('http://adsabs.harvard.edu/abs/2016GeCoA.173..264S','NASAADS'); return false;" href="http://adsabs.harvard.edu/abs/2016GeCoA.173..264S"><span>Variations in microbial carbon sources and cycling in the deep continental subsurface</span></a></p> <p><a target="_blank" rel="noopener noreferrer" href="http://adsabs.harvard.edu/abstract_service.html">NASA Astrophysics Data System (ADS)</a></p> <p>Simkus, Danielle N.; Slater, Greg F.; Lollar, Barbara Sherwood; Wilkie, Kenna; Kieft, Thomas L.; Magnabosco, Cara; Lau, Maggie C. Y.; Pullin, Michael J.; Hendrickson, Sarah B.; Wommack, K. Eric; Sakowski, Eric G.; van Heerden, Esta; Kuloyo, Olukayode; Linage, Borja; Borgonie, Gaetan; Onstott, Tullis C.</p> <p>2016-01-01</p> <p>Deep continental subsurface fracture water systems, ranging from 1.1 to 3.3 km below land surface (kmbls), were investigated to characterize the indigenous microorganisms and elucidate microbial carbon sources and their cycling. Analysis of phospholipid fatty acid (PLFA) abundances and direct cell counts detected varying biomass that was not correlated with depth. Compound-specific carbon isotope analyses (δ13C and Δ14C) of the phospholipid fatty acids (PLFAs) and carbon substrates combined with genomic analyses did identify, however, distinct carbon sources and cycles between the two depth ranges studied. In the shallower boreholes at circa 1 kmbls, isotopic evidence indicated microbial incorporation of biogenic CH4 by the in situ microbial community. At the shallowest site, 1.05 kmbls in Driefontein mine, this process clearly dominated the isotopic signal. At slightly deeper depths, 1.34 kmbls in Beatrix mine, the isotopic data indicated the incorporation of both biogenic CH4 and dissolved inorganic carbon (DIC) derived from CH4 oxidation. In both of these cases, molecular genetic analysis indicated that methanogenic and methanotrophic organisms together comprised a small component (<5%) of the microbial community. Thus, it appears that a relatively minor component of the prokaryotic community is supporting a much larger overall bacterial community in these samples. In the samples collected from >3 kmbls in Tau Tona mine (TT107, TT109 Bh2), the CH4 had an isotopic signature suggesting a predominantly abiogenic origin with minor inputs from microbial methanogenesis. In these samples, the isotopic enrichments (δ13C and Δ14C) of the PLFAs relative to CH4 were consistent with little incorporation of CH4 into the biomass. The most 13C-enriched PLFAs were observed in TT107 where the dominant CO2-fixation pathway was the acetyl-CoA pathway by non-acetogenic bacteria. The differences in the δ13C of the PLFAs and the DIC and DOC for TT109 Bh2 were ∼-24‰ and 0‰, respectively. The dominant CO2-fixation pathways were 3-HP/4-HB cycle > acetyl-CoA pathway > reductive pentose phosphate cycle.</p> </li> <li> <p><a target="_blank" rel="noopener noreferrer" onclick="trackOutboundLink('https://www.pubmedcentral.nih.gov/articlerender.fcgi?tool=pmcentrez&artid=5518199','PMC'); return false;" href="https://www.pubmedcentral.nih.gov/articlerender.fcgi?tool=pmcentrez&artid=5518199"><span>Microbial potential for carbon and nutrient cycling in a geogenic supercritical carbon dioxide reservoir</span></a></p> <p><a target="_blank" rel="noopener noreferrer" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?DB=pmc">PubMed Central</a></p> <p>Freedman, Adam J.E.; Tan, BoonFei</p> <p>2017-01-01</p> <p>Summary Microorganisms catalyze carbon cycling and biogeochemical reactions in the deep subsurface and thus may be expected to influence the fate of injected supercritical (sc) CO2 following geological carbon sequestration (GCS). We hypothesized that natural subsurface scCO2 reservoirs, which serve as analogs for the long‐term fate of sequestered scCO2, harbor a ‘deep carbonated biosphere’ with carbon cycling potential. We sampled subsurface fluids from scCO2‐water separators at a natural scCO2 reservoir at McElmo Dome, Colorado for analysis of 16S rRNA gene diversity and metagenome content. Sequence annotations indicated dominance of Sulfurospirillum, Rhizobium, Desulfovibrio and four members of the Clostridiales family. Genomes extracted from metagenomes using homology and compositional approaches revealed diverse mechanisms for growth and nutrient cycling, including pathways for CO2 and N2 fixation, anaerobic respiration, sulfur oxidation, fermentation and potential for metabolic syntrophy. Differences in biogeochemical potential between two production well communities were consistent with differences in fluid chemical profiles, suggesting a potential link between microbial activity and geochemistry. The existence of a microbial ecosystem associated with the McElmo Dome scCO2 reservoir indicates that potential impacts of the deep biosphere on CO2 fate and transport should be taken into consideration as a component of GCS planning and modelling. PMID:28229521</p> </li> <li> <p><a target="_blank" rel="noopener noreferrer" onclick="trackOutboundLink('http://adsabs.harvard.edu/abs/2017AGUFMGC43C1075N','NASAADS'); return false;" href="http://adsabs.harvard.edu/abs/2017AGUFMGC43C1075N"><span>How does soil erosion influence the terrestrial carbon cycle and the impacts of land use and land cover change?</span></a></p> <p><a target="_blank" rel="noopener noreferrer" href="http://adsabs.harvard.edu/abstract_service.html">NASA Astrophysics Data System (ADS)</a></p> <p>Naipal, V.; Wang, Y.; Ciais, P.; Guenet, B.; Lauerwald, R.</p> <p>2017-12-01</p> <p>The onset of agriculture has accelerated soil erosion rates significantly, mobilizing vast quantities of soil organic carbon (SOC) globally. Studies show that at timescales of decennia to millennia this mobilized SOC can significantly alter previously estimated carbon emissions from land use and land cover change (LULCC). However, a full understanding of the impact of soil erosion on land-atmosphere carbon exchange is still missing. The aim of our study is to better constrain the terrestrial carbon fluxes by developing methods, which are compatible with earth system models (ESMs), and explicitly represent the links between soil erosion and carbon dynamics. For this we use an emulator that represents the carbon cycle of ORCHIDEE, which is the land component of the IPSL ESM, in combination with an adjusted version of the Revised Universal Soil Loss Equation (RUSLE) model. We applied this modeling framework at the global scale to evaluate how soil erosion influenced the terrestrial carbon cycle in the presence of elevated CO2, regional climate change and land use change. Here, we focus on the effects of soil detachment by erosion only and do not consider sediment transport and deposition. We found that including soil erosion in the SOC dynamics-scheme resulted in two times more SOC being lost during the historical period (1850-2005 AD). LULCC is the main contributor to this SOC loss, whose impact on the SOC stocks is significantly amplified by erosion. Regionally, the influence of soil erosion varies significantly, depending on the magnitude of the perturbations to the carbon cycle and the effects of LULCC and climate change on soil erosion rates. We conclude that it is necessary to include soil erosion in assessments of LULCC, and to explicitly consider the effects of elevated CO2 and climate change on the carbon cycle and on soil erosion, for better quantification of past, present, and future LULCC carbon emissions.</p> </li> <li> <p><a target="_blank" rel="noopener noreferrer" onclick="trackOutboundLink('https://www.ncbi.nlm.nih.gov/pubmed/28772731','PUBMED'); return false;" href="https://www.ncbi.nlm.nih.gov/pubmed/28772731"><span>Effects of Electrospun Carbon Nanofibers' Interlayers on High-Performance Lithium-Sulfur Batteries.</span></a></p> <p><a target="_blank" rel="noopener noreferrer" href="https://www.ncbi.nlm.nih.gov/entrez/query.fcgi?DB=pubmed">PubMed</a></p> <p>Gao, Tianji; Le, TrungHieu; Yang, Ying; Yu, Zhihao; Huang, Zhenghong; Kang, Feiyu</p> <p>2017-03-31</p> <p>Two different interlayers were introduced in lithium-sulfur batteries to improve the cycling stability with sulfur loading as high as 80% of total mass of cathode. Melamine was recommended as a nitrogen-rich (N-rich) amine component to synthesize a modified polyacrylic acid (MPAA). The electrospun MPAA was carbonized into N-rich carbon nanofibers, which were used as cathode interlayers, while carbon nanofibers from PAA without melamine was used as an anode interlayer. At the rate of 0.1 C, the initial discharge capacity with two interlayers was 983 mAh g -1 , and faded down to 651 mAh g -1 after 100 cycles with the coulombic efficiency of 95.4%. At the rate of 1 C, the discharge capacity was kept to 380 mAh g -1 after 600 cycles with a coulombic efficiency of 98.8%. It apparently demonstrated that the cathode interlayer is extremely effective at shutting down the migration of polysulfide ions. The anode interlayer induced the lithium ions to form uniform lithium metal deposits confined on the fiber surface and in the bulk to strengthen the cycling stability of the lithium metal anode.</p> </li> </ol> <div class="pull-right"> <ul class="pagination"> <li><a href="#" onclick='return showDiv("page_1");'>«</a></li> <li><a href="#" onclick='return showDiv("page_3");'>3</a></li> <li><a href="#" onclick='return showDiv("page_4");'>4</a></li> <li class="active"><span>5</span></li> <li><a href="#" onclick='return showDiv("page_6");'>6</a></li> <li><a href="#" onclick='return showDiv("page_7");'>7</a></li> <li><a href="#" onclick='return showDiv("page_25");'>»</a></li> </ul> </div> </div><!-- col-sm-12 --> </div><!-- row --> </div><!-- page_5 --> <div id="page_6" class="hiddenDiv"> <div class="row"> <div class="col-sm-12"> <div class="pull-right"> <ul class="pagination"> <li><a href="#" onclick='return showDiv("page_1");'>«</a></li> <li><a href="#" onclick='return showDiv("page_4");'>4</a></li> <li><a href="#" onclick='return showDiv("page_5");'>5</a></li> <li class="active"><span>6</span></li> <li><a href="#" onclick='return showDiv("page_7");'>7</a></li> <li><a href="#" onclick='return showDiv("page_8");'>8</a></li> <li><a href="#" onclick='return showDiv("page_25");'>»</a></li> </ul> </div> </div> </div> <div class="row"> <div class="col-sm-12"> <ol class="result-class" start="101"> <li> <p><a target="_blank" rel="noopener noreferrer" onclick="trackOutboundLink('https://www.pubmedcentral.nih.gov/articlerender.fcgi?tool=pmcentrez&artid=5506899','PMC'); return false;" href="https://www.pubmedcentral.nih.gov/articlerender.fcgi?tool=pmcentrez&artid=5506899"><span>Effects of Electrospun Carbon Nanofibers’ Interlayers on High-Performance Lithium–Sulfur Batteries</span></a></p> <p><a target="_blank" rel="noopener noreferrer" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?DB=pmc">PubMed Central</a></p> <p>Gao, Tianji; Le, TrungHieu; Yang, Ying; Yu, Zhihao; Huang, Zhenghong; Kang, Feiyu</p> <p>2017-01-01</p> <p>Two different interlayers were introduced in lithium–sulfur batteries to improve the cycling stability with sulfur loading as high as 80% of total mass of cathode. Melamine was recommended as a nitrogen-rich (N-rich) amine component to synthesize a modified polyacrylic acid (MPAA). The electrospun MPAA was carbonized into N-rich carbon nanofibers, which were used as cathode interlayers, while carbon nanofibers from PAA without melamine was used as an anode interlayer. At the rate of 0.1 C, the initial discharge capacity with two interlayers was 983 mAh g−1, and faded down to 651 mAh g−1 after 100 cycles with the coulombic efficiency of 95.4%. At the rate of 1 C, the discharge capacity was kept to 380 mAh g−1 after 600 cycles with a coulombic efficiency of 98.8%. It apparently demonstrated that the cathode interlayer is extremely effective at shutting down the migration of polysulfide ions. The anode interlayer induced the lithium ions to form uniform lithium metal deposits confined on the fiber surface and in the bulk to strengthen the cycling stability of the lithium metal anode. PMID:28772731</p> </li> <li> <p><a target="_blank" rel="noopener noreferrer" onclick="trackOutboundLink('https://www.ncbi.nlm.nih.gov/pubmed/22717174','PUBMED'); return false;" href="https://www.ncbi.nlm.nih.gov/pubmed/22717174"><span>All-solid-state flexible supercapacitors fabricated with bacterial nanocellulose papers, carbon nanotubes, and triblock-copolymer ion gels.</span></a></p> <p><a target="_blank" rel="noopener noreferrer" href="https://www.ncbi.nlm.nih.gov/entrez/query.fcgi?DB=pubmed">PubMed</a></p> <p>Kang, Yu Jin; Chun, Sang-Jin; Lee, Sung-Suk; Kim, Bo-Yeong; Kim, Jung Hyeun; Chung, Haegeun; Lee, Sun-Young; Kim, Woong</p> <p>2012-07-24</p> <p>We demonstrate all-solid-state flexible supercapacitors with high physical flexibility, desirable electrochemical properties, and excellent mechanical integrity, which were realized by rationally exploiting unique properties of bacterial nanocellulose, carbon nanotubes, and ionic liquid based polymer gel electrolytes. This deliberate choice and design of main components led to excellent supercapacitor performance such as high tolerance against bending cycles and high capacitance retention over charge/discharge cycles. More specifically, the performance of our supercapacitors was highly retained through 200 bending cycles to a radius of 3 mm. In addition, the supercapacitors showed excellent cyclability with C(sp) (~20 mF/cm(2)) reduction of only <0.5% over 5000 charge/discharge cycles at the current density of 10 A/g. Our demonstration could be an important basis for material design and development of flexible supercapacitors.</p> </li> <li> <p><a target="_blank" rel="noopener noreferrer" onclick="trackOutboundLink('http://adsabs.harvard.edu/abs/1990ECSS...30..641R','NASAADS'); return false;" href="http://adsabs.harvard.edu/abs/1990ECSS...30..641R"><span>Nature of POC transport in a mangrove ecosystem: A carbon stable isotopic study</span></a></p> <p><a target="_blank" rel="noopener noreferrer" href="http://adsabs.harvard.edu/abstract_service.html">NASA Astrophysics Data System (ADS)</a></p> <p>Rezende, C. E.; Lacerda, L. D.; Ovall, A. R. C.; Silva, C. A. R.; Martinelli, L. A.</p> <p>1990-06-01</p> <p>The isotopic composition of particulate organic carbon (POC) was studied during five tidal cycles in a mangrove creek of Sepetiba Bay, Rio de Janeiro, Brazil. The results show that a mixture of organic carbon from mangrove and marine origins is always present in the creek. Mean mangrove contribution to the POC varied from 16% to 100% and was dependent on tidal amplitude. The results suggest that oceanic carbon can be an important component of carbon balance in mangrove ecosystems. Therefore, earlier carbon balance studies from mangroves which did not include measurements of carbon isotopic composition should be interpreted with care.</p> </li> <li> <p><a target="_blank" rel="noopener noreferrer" onclick="trackOutboundLink('https://www.fs.usda.gov/treesearch/pubs/40567','TREESEARCH'); return false;" href="https://www.fs.usda.gov/treesearch/pubs/40567"><span>Effects of watershed history on dissolved organic matter characteristics in headwater streams</span></a></p> <p><a target="_blank" rel="noopener noreferrer" href="http://www.fs.usda.gov/treesearch/">Treesearch</a></p> <p>Youhei Yamashita; Brian D. Kloeppel; Jennifer Knoepp; Gregory L. Zausen; Rudolf Jaffe'</p> <p>2011-01-01</p> <p>Dissolved organic matter (DOM) is recognized as a major component in the global carbon cycle and is an important driver in aquatic ecosystem function. Climate, land use, and forest cover changes all impact stream DOM and alter biogeochemical cycles in terrestrial environments. We determined the temporal variation in DOM quantity and quality in headwater streams at a...</p> </li> <li> <p><a target="_blank" rel="noopener noreferrer" onclick="trackOutboundLink('https://www.fs.usda.gov/treesearch/pubs/49542','TREESEARCH'); return false;" href="https://www.fs.usda.gov/treesearch/pubs/49542"><span>Dissolved organic carbon fluxes from hydropedologic units in Alaskan coastal temperate rainforest watersheds</span></a></p> <p><a target="_blank" rel="noopener noreferrer" href="http://www.fs.usda.gov/treesearch/">Treesearch</a></p> <p>David V. D' Amore; Rick T. Edwards; Paul A. Herendeen; Eran Hood; Jason B. Fellman</p> <p>2015-01-01</p> <p>Dissolved organic C (DOC) transfer from the landscape to coastal margins is a key component of regional C cycles. Hydropedology provides a conceptual and observational framework for linking soil hydrologic function to landscape C cycling. We used hydropedology to quantify the export of DOC from the terrestrial landscape and understand how soil temperature and water...</p> </li> <li> <p><a target="_blank" rel="noopener noreferrer" onclick="trackOutboundLink('https://www.fs.usda.gov/treesearch/pubs/34379','TREESEARCH'); return false;" href="https://www.fs.usda.gov/treesearch/pubs/34379"><span>Response of carbon fluxes to drought in a coastal plain loblolly pine forest</span></a></p> <p><a target="_blank" rel="noopener noreferrer" href="http://www.fs.usda.gov/treesearch/">Treesearch</a></p> <p>Asko Noormets; Michael J. Gavazzi; Steve G. McNulty; Jean-Christophe Domec; Ge Sun; John S. King; Jiquan Chen</p> <p>2010-01-01</p> <p>Full accounting of ecosystem carbon (C) pools and fluxes in coastal plain ecosystems remains less studied compared with upland systems, even though the C stocks in these systems may be up to an order of magnitude higher, making them a potentially important component in regional C cycle. Here, we report C pools and CO2 exchange rates...</p> </li> <li> <p><a target="_blank" rel="noopener noreferrer" onclick="trackOutboundLink('https://www.fs.usda.gov/treesearch/pubs/20282','TREESEARCH'); return false;" href="https://www.fs.usda.gov/treesearch/pubs/20282"><span>An integrated model of soil, hydrology, and vegetation for carbon dynamics in wetland ecosystems</span></a></p> <p><a target="_blank" rel="noopener noreferrer" href="http://www.fs.usda.gov/treesearch/">Treesearch</a></p> <p>Yu Zhang; Changsheng Li; Carl C. Trettin; Harbin Li; Ge Sun</p> <p>2002-01-01</p> <p>Wetland ecosystems are an important component in global carbon (C) cycles and may exert a large influence on global clinlate change. Predictions of C dynamics require us to consider interactions among many critical factors of soil, hydrology, and vegetation. However, few such integrated C models exist for wetland ecosystems. In this paper, we report a simulation model...</p> </li> <li> <p><a target="_blank" rel="noopener noreferrer" onclick="trackOutboundLink('https://pubs.er.usgs.gov/publication/70168804','USGSPUBS'); return false;" href="https://pubs.er.usgs.gov/publication/70168804"><span>Nitrogen attenuation of terrestrial carbon cycle response to global environmental factors</span></a></p> <p><a target="_blank" rel="noopener noreferrer" href="http://pubs.er.usgs.gov/pubs/index.jsp?view=adv">USGS Publications Warehouse</a></p> <p>Jain, A.A.; Yang, Xiaojuan; Kheshgi, H.; McGuire, A. David; Post, W.; Kicklighter, David W.</p> <p>2009-01-01</p> <p>Nitrogen cycle dynamics have the capacity to attenuate the magnitude of global terrestrial carbon sinks and sources driven by CO2 fertilization and changes in climate. In this study, two versions of the terrestrial carbon and nitrogen cycle components of the Integrated Science Assessment Model (ISAM) are used to evaluate how variation in nitrogen availability influences terrestrial carbon sinks and sources in response to changes over the 20th century in global environmental factors including atmospheric CO2 concentration, nitrogen inputs, temperature, precipitation and land use. The two versions of ISAM vary in their treatment of nitrogen availability: ISAM-NC has a terrestrial carbon cycle model coupled to a fully dynamic nitrogen cycle while ISAM-C has an identical carbon cycle model but nitrogen availability is always in sufficient supply. Overall, the two versions of the model estimate approximately the same amount of global mean carbon uptake over the 20th century. However, comparisons of results of ISAM-NC relative to ISAM-C reveal that nitrogen dynamics: (1) reduced the 1990s carbon sink associated with increasing atmospheric CO2 by 0.53 PgC yr−1 (1 Pg = 1015g), (2) reduced the 1990s carbon source associated with changes in temperature and precipitation of 0.34 PgC yr−1 in the 1990s, (3) an enhanced sink associated with nitrogen inputs by 0.26 PgC yr−1, and (4) enhanced the 1990s carbon source associated with changes in land use by 0.08 PgC yr−1 in the 1990s. These effects of nitrogen limitation influenced the spatial distribution of the estimated exchange of CO2 with greater sink activity in high latitudes associated with climate effects and a smaller sink of CO2 in the southeastern United States caused by N limitation associated with both CO2 fertilization and forest regrowth. These results indicate that the dynamics of nitrogen availability are important to consider in assessing the spatial distribution and temporal dynamics of terrestrial carbon sources and sinks.</p> </li> <li> <p><a target="_blank" rel="noopener noreferrer" onclick="trackOutboundLink('http://adsabs.harvard.edu/abs/2016AGUOSCT44A0204R','NASAADS'); return false;" href="http://adsabs.harvard.edu/abs/2016AGUOSCT44A0204R"><span>Environmental Dynamics of Dissolved Black Carbon in the Amazon River</span></a></p> <p><a target="_blank" rel="noopener noreferrer" href="http://adsabs.harvard.edu/abstract_service.html">NASA Astrophysics Data System (ADS)</a></p> <p>Roebuck, J. A., Jr.; Gonsior, M.; Enrich-Prast, A.; Jaffe, R.</p> <p>2016-02-01</p> <p>Dissolve black carbon (DBC) is an important component in the global carbon cycle and constitutes a significant portion of dissolved organic carbon (DOC) in aquatic systems. While global fluxes of DBC may be well understood, little is known about systematic processing of this carbon pool in fluvial systems. Similar to DOC, DBC composition may change as it moves throughout a river continuum before it is eventually deposited into the ocean. This is especially important for large river systems that are major sources of DOC to the ocean and may have significant impacts on ocean biogeochemistry and carbon cycling. To better understand variations in DBC dynamics throughout a large fluvial system, DBC was quantified using the benzene polycarboxylic acid method (BPCA) in three major tributaries of the Amazon River, each with varying biogeochemical characteristics. Principal component analysis of the BPCA abundances was used to assess the DBC compositional differences between sampling locations. In some rivers, light availability appeared to influence both DBC quantity and quality. Higher concentrations of DBC characterized by a larger, more aromatic DBC pool was found in the Rio Negro, a black water river with high levels of chromophoric dissolved organic matter and low light penetration. In the Rio Tapajós, a clear water river with higher light penetration, lower DBC concentrations characterized by higher abundances of the less polycondensed DBC pool provided evidence of photodecomposition under such conditions. The Rio Madeira, characterized as a white water river with high suspended sediment yields and high mineral/clay content, had the lowest DBC concentrations and the least polycondensed DBC content, suggesting a preferential adsorption of the more highly polycondensed DBC components onto clay particles.</p> </li> <li> <p><a target="_blank" rel="noopener noreferrer" onclick="trackOutboundLink('https://www.ncbi.nlm.nih.gov/pubmed/28906052','PUBMED'); return false;" href="https://www.ncbi.nlm.nih.gov/pubmed/28906052"><span>Forest biomass, productivity and carbon cycling along a rainfall gradient in West Africa.</span></a></p> <p><a target="_blank" rel="noopener noreferrer" href="https://www.ncbi.nlm.nih.gov/entrez/query.fcgi?DB=pubmed">PubMed</a></p> <p>Moore, Sam; Adu-Bredu, Stephen; Duah-Gyamfi, Akwasi; Addo-Danso, Shalom D; Ibrahim, Forzia; Mbou, Armel T; de Grandcourt, Agnès; Valentini, Riccardo; Nicolini, Giacomo; Djagbletey, Gloria; Owusu-Afriyie, Kennedy; Gvozdevaite, Agne; Oliveras, Imma; Ruiz-Jaen, Maria C; Malhi, Yadvinder</p> <p>2018-02-01</p> <p>Net Primary Productivity (NPP) is one of the most important parameters in describing the functioning of any ecosystem and yet it arguably remains a poorly quantified and understood component of carbon cycling in tropical forests, especially outside of the Americas. We provide the first comprehensive analysis of NPP and its carbon allocation to woody, canopy and root growth components at contrasting lowland West African forests spanning a rainfall gradient. Using a standardized methodology to study evergreen (EF), semi-deciduous (SDF), dry forests (DF) and woody savanna (WS), we find that (i) climate is more closely related with above and belowground C stocks than with NPP (ii) total NPP is highest in the SDF site, then the EF followed by the DF and WS and that (iii) different forest types have distinct carbon allocation patterns whereby SDF allocate in excess of 50% to canopy production and the DF and WS sites allocate 40%-50% to woody production. Furthermore, we find that (iv) compared with canopy and root growth rates the woody growth rate of these forests is a poor proxy for their overall productivity and that (v) residence time is the primary driver in the productivity-allocation-turnover chain for the observed spatial differences in woody, leaf and root biomass across the rainfall gradient. Through a systematic assessment of forest productivity we demonstrate the importance of directly measuring the main components of above and belowground NPP and encourage the establishment of more permanent carbon intensive monitoring plots across the tropics. © 2017 John Wiley & Sons Ltd.</p> </li> <li> <p><a target="_blank" rel="noopener noreferrer" onclick="trackOutboundLink('https://www.fs.usda.gov/treesearch/pubs/47052','TREESEARCH'); return false;" href="https://www.fs.usda.gov/treesearch/pubs/47052"><span>Can current moisture responses predict soil CO2 efflux under altered precipitation regimes? A synthesis of manipulation experiments</span></a></p> <p><a target="_blank" rel="noopener noreferrer" href="http://www.fs.usda.gov/treesearch/">Treesearch</a></p> <p>S. Vicca; M. Bahn; M. Estiarte; E. E. van Loon; R. Vargas; G. Alberti; P. Ambus; M. A. Arain; C. Beier; L. P. Bentley; W. Borken; N. Buchmann; S. L. Collins; G. de Dato; J. S. Dukes; C. Escolar; P. Fay; G. Guidolotti; P. J. Hanson; A. Kahmen; G. Kröel-Dulay; T. Ladreiter-Knauss; K. S. Larsen; E. Lellei-Kovacs; E. Lebrija-Trejos; F. T. Maestre; S. Marhan; M. Marshall; P. Meir; Y. Miao; J. Muhr; P. A. Niklaus; R. Ogaya; J. Peñuelas; C. Poll; L. E. Rustad; K. Savage; A. Schindlbacher; I. K. Schmidt; A. R. Smith; E. D. Sotta; V. Suseela; A. Tietema; N. van Gestel; O. van Straaten; S. Wan; U. Weber; I. A. Janssens</p> <p>2014-01-01</p> <p>As a key component of the carbon cycle, soil CO2 efflux (SCE) is being increasingly studied to improve our mechanistic understanding of this important carbon flux. Predicting ecosystem responses to climate change often depends an extrapolation of current relationships between ecosystem processes and their climatic drivers to conditions not yet experienced by the...</p> </li> <li> <p><a target="_blank" rel="noopener noreferrer" onclick="trackOutboundLink('https://www.fs.usda.gov/treesearch/pubs/50315','TREESEARCH'); return false;" href="https://www.fs.usda.gov/treesearch/pubs/50315"><span>The role of old forests and big trees in forest carbon sequestration in the Pacific Northwest</span></a></p> <p><a target="_blank" rel="noopener noreferrer" href="http://www.fs.usda.gov/treesearch/">Treesearch</a></p> <p>Andrew N. Gray</p> <p>2015-01-01</p> <p>Forest ecosystems are an important component of the global carbon (C) cycle. Recent research has indicated that large trees in general, and old-growth forests in particular, sequester substantial amounts of C annually. C sequestration rates are thought to peak and decline with stand age but the timing and controls are not well-understood. The objectives of this study...</p> </li> <li> <p><a target="_blank" rel="noopener noreferrer" onclick="trackOutboundLink('https://www.fs.usda.gov/treesearch/pubs/52283','TREESEARCH'); return false;" href="https://www.fs.usda.gov/treesearch/pubs/52283"><span>Total belowground carbon flux in subalpine forests is related to leaf area index, soil nitrogen, and tree height</span></a></p> <p><a target="_blank" rel="noopener noreferrer" href="http://www.fs.usda.gov/treesearch/">Treesearch</a></p> <p>E. Berryman; Michael Ryan; J. B. Bradford; T. J. Hawbaker; R. Birdsey</p> <p>2016-01-01</p> <p>In forests, total belowground carbon (C) flux (TBCF) is a large component of the C budget and represents a critical pathway for delivery of plant C to soil. Reducing uncertainty around regional estimates of forest C cycling may be aided by incorporating knowledge of controls over soil respiration and TBCF. Photosynthesis, and presumably TBCF, declines with...</p> </li> <li> <p><a target="_blank" rel="noopener noreferrer" onclick="trackOutboundLink('http://adsabs.harvard.edu/abs/2017AGUFM.B43I..02P','NASAADS'); return false;" href="http://adsabs.harvard.edu/abs/2017AGUFM.B43I..02P"><span>Ten years of multiple data stream assimilation with the ORCHIDEE land surface model to improve regional to global simulated carbon budgets: synthesis and perspectives on directions for the future</span></a></p> <p><a target="_blank" rel="noopener noreferrer" href="http://adsabs.harvard.edu/abstract_service.html">NASA Astrophysics Data System (ADS)</a></p> <p>Peylin, P. P.; Bacour, C.; MacBean, N.; Maignan, F.; Bastrikov, V.; Chevallier, F.</p> <p>2017-12-01</p> <p>Predicting the fate of carbon stocks and their sensitivity to climate change and land use/management strongly relies on our ability to accurately model net and gross carbon fluxes. However, simulated carbon and water fluxes remain subject to large uncertainties, partly because of unknown or poorly calibrated parameters. Over the past ten years, the carbon cycle data assimilation system at the Laboratoire des Sciences du Climat et de l'Environnement has investigated the benefit of assimilating multiple carbon cycle data streams into the ORCHIDEE LSM, the land surface component of the Institut Pierre Simon Laplace Earth System Model. These datasets have included FLUXNET eddy covariance data (net CO2 flux and latent heat flux) to constrain hourly to seasonal time-scale carbon cycle processes, remote sensing of the vegetation activity (MODIS NDVI) to constrain the leaf phenology, biomass data to constrain "slow" (yearly to decadal) processes of carbon allocation, and atmospheric CO2 concentrations to provide overall large scale constraints on the land carbon sink. Furthermore, we have investigated technical issues related to multiple data stream assimilation and choice of optimization algorithm. This has provided a wide-ranging perspective on the challenges we face in constraining model parameters and thus better quantifying, and reducing, model uncertainty in projections of the future global carbon sink. We review our past studies in terms of the impact of the optimization on key characteristics of the carbon cycle, e.g. the partition of the northern latitudes vs tropical land carbon sink, and compare to the classic atmospheric flux inversion approach. Throughout, we discuss our work in context of the abovementioned challenges, and propose solutions for the community going forward, including the potential of new observations such as atmospheric COS concentrations and satellite-derived Solar Induced Fluorescence to constrain the gross carbon fluxes of the ORCHIDEE model.</p> </li> <li> <p><a target="_blank" rel="noopener noreferrer" onclick="trackOutboundLink('https://www.ncbi.nlm.nih.gov/pubmed/28229521','PUBMED'); return false;" href="https://www.ncbi.nlm.nih.gov/pubmed/28229521"><span>Microbial potential for carbon and nutrient cycling in a geogenic supercritical carbon dioxide reservoir.</span></a></p> <p><a target="_blank" rel="noopener noreferrer" href="https://www.ncbi.nlm.nih.gov/entrez/query.fcgi?DB=pubmed">PubMed</a></p> <p>Freedman, Adam J E; Tan, BoonFei; Thompson, Janelle R</p> <p>2017-06-01</p> <p>Microorganisms catalyze carbon cycling and biogeochemical reactions in the deep subsurface and thus may be expected to influence the fate of injected supercritical (sc) CO 2 following geological carbon sequestration (GCS). We hypothesized that natural subsurface scCO 2 reservoirs, which serve as analogs for the long-term fate of sequestered scCO 2 , harbor a 'deep carbonated biosphere' with carbon cycling potential. We sampled subsurface fluids from scCO 2 -water separators at a natural scCO 2 reservoir at McElmo Dome, Colorado for analysis of 16S rRNA gene diversity and metagenome content. Sequence annotations indicated dominance of Sulfurospirillum, Rhizobium, Desulfovibrio and four members of the Clostridiales family. Genomes extracted from metagenomes using homology and compositional approaches revealed diverse mechanisms for growth and nutrient cycling, including pathways for CO 2 and N 2 fixation, anaerobic respiration, sulfur oxidation, fermentation and potential for metabolic syntrophy. Differences in biogeochemical potential between two production well communities were consistent with differences in fluid chemical profiles, suggesting a potential link between microbial activity and geochemistry. The existence of a microbial ecosystem associated with the McElmo Dome scCO 2 reservoir indicates that potential impacts of the deep biosphere on CO 2 fate and transport should be taken into consideration as a component of GCS planning and modelling. © 2017 The Authors. Environmental Microbiology published by Society for Applied Microbiology and John Wiley & Sons Ltd.</p> </li> <li> <p><a target="_blank" rel="noopener noreferrer" onclick="trackOutboundLink('http://adsabs.harvard.edu/abs/2015PhDT........75K','NASAADS'); return false;" href="http://adsabs.harvard.edu/abs/2015PhDT........75K"><span>Climate and Management Controls on Forest Growth and Forest Carbon Balance in the Western United States</span></a></p> <p><a target="_blank" rel="noopener noreferrer" href="http://adsabs.harvard.edu/abstract_service.html">NASA Astrophysics Data System (ADS)</a></p> <p>Kelsey, Katharine Cashman</p> <p></p> <p>Climate change is resulting in a number of rapid changes in forests worldwide. Forests comprise a critical component of the global carbon cycle, and therefore climate-induced changes in forest carbon balance have the potential to create a feedback within the global carbon cycle and affect future trajectories of climate change. In order to further understanding of climate-driven changes in forest carbon balance, I (1) develop a method to improve spatial estimates forest carbon stocks, (2) investigate the effect of climate change and forest management actions on forest recovery and carbon balance following disturbance, and (3) explore the relationship between climate and forest growth, and identify climate-driven trends in forest growth through time, within San Juan National Forest in southwest Colorado, USA. I find that forest carbon estimates based on texture analysis from LandsatTM imagery improve regional forest carbon maps, and this method is particularly useful for estimating carbon stocks in forested regions affected by disturbance. Forest recovery from disturbance is also a critical component of future forest carbon stocks, and my results indicate that both climate and forest management actions have important implications for forest recovery and carbon dynamics following disturbance. Specifically, forest treatments that use woody biomass removed from the forest for electricity production can reduce carbon emissions to the atmosphere, but climate driven changes in fire severity and forest recovery can have the opposite effect on forest carbon stocks. In addition to the effects of disturbance and recovery on forest condition, I also find that climate change is decreasing rates of forest growth in some species, likely in response to warming summer temperatures. These growth declines could result in changes of vegetation composition, or in extreme cases, a shift in vegetation type that would alter forest carbon storage. This work provides insight into both current and future changes in forest carbon balance as a consequence of climate change and forest management in the western US.</p> </li> <li> <p><a target="_blank" rel="noopener noreferrer" onclick="trackOutboundLink('https://www.ncbi.nlm.nih.gov/pubmed/21921159','PUBMED'); return false;" href="https://www.ncbi.nlm.nih.gov/pubmed/21921159"><span>Deep mantle cycling of oceanic crust: evidence from diamonds and their mineral inclusions.</span></a></p> <p><a target="_blank" rel="noopener noreferrer" href="https://www.ncbi.nlm.nih.gov/entrez/query.fcgi?DB=pubmed">PubMed</a></p> <p>Walter, M J; Kohn, S C; Araujo, D; Bulanova, G P; Smith, C B; Gaillou, E; Wang, J; Steele, A; Shirey, S B</p> <p>2011-10-07</p> <p>A primary consequence of plate tectonics is that basaltic oceanic crust subducts with lithospheric slabs into the mantle. Seismological studies extend this process to the lower mantle, and geochemical observations indicate return of oceanic crust to the upper mantle in plumes. There has been no direct petrologic evidence, however, of the return of subducted oceanic crustal components from the lower mantle. We analyzed superdeep diamonds from Juina-5 kimberlite, Brazil, which host inclusions with compositions comprising the entire phase assemblage expected to crystallize from basalt under lower-mantle conditions. The inclusion mineralogies require exhumation from the lower to upper mantle. Because the diamond hosts have carbon isotope signatures consistent with surface-derived carbon, we conclude that the deep carbon cycle extends into the lower mantle.</p> </li> <li> <p><a target="_blank" rel="noopener noreferrer" onclick="trackOutboundLink('https://www.ncbi.nlm.nih.gov/pubmed/25971033','PUBMED'); return false;" href="https://www.ncbi.nlm.nih.gov/pubmed/25971033"><span>Hierarchical porous carbon/MnO2 hybrids as supercapacitor electrodes.</span></a></p> <p><a target="_blank" rel="noopener noreferrer" href="https://www.ncbi.nlm.nih.gov/entrez/query.fcgi?DB=pubmed">PubMed</a></p> <p>Lee, Min Eui; Yun, Young Soo; Jin, Hyoung-Joon</p> <p>2014-12-01</p> <p>Hybrid electrodes of hierarchical porous carbon (HPC) and manganese oxide (MnO2) were synthesized using a fast surface redox reaction of potassium permanganate under facile immersion methods. The HPC/MnO2 hybrids had a number of micropores and macropores and the MnO2 nanoparticles acted as a pseudocapacitive material. The synergistic effects of electric double-layer capacitor (EDLC)-induced capacitance and pseudocapacitance brought about a better electrochemical performance of the HPC/MnO2 hybrid electrodes compared to that obtained with a single component. The hybrids showed a specific capacitance of 228 F g(-1) and good cycle stability over 1000 cycles.</p> </li> <li> <p><a target="_blank" rel="noopener noreferrer" onclick="trackOutboundLink('https://www.ncbi.nlm.nih.gov/pubmed/25796917','PUBMED'); return false;" href="https://www.ncbi.nlm.nih.gov/pubmed/25796917"><span>[Research progress on carbon sink function of agroforestry system under climate change].</span></a></p> <p><a target="_blank" rel="noopener noreferrer" href="https://www.ncbi.nlm.nih.gov/entrez/query.fcgi?DB=pubmed">PubMed</a></p> <p>Xie, Ting-Ting; Su, Pei-Xi; Zhou, Zi-Juan; Shan, Li-Shan</p> <p>2014-10-01</p> <p>As a land comprehensive utilization system, agroforestry system can absorb and fix CO2 effectively to increase carbon storage, and also reduces greenhouse effect convincingly while reaching the aim of harvest. The regulatory role in CO2 makes humans realize that agroforestry systems have significant superiority compared with single cropping systems, therefore, understanding the carbon sinks of different components in an agroforestry system and its influencing factors play an important role in studying global carbon cycle and accurate evaluation of carbon budget. This paper reviewed the concept and classification of agroforestry system, and then the carbon sequestration potentials of different components in agroforestry systems and influencing factors. It was concluded that the carbon sequestration rate of plants from different agroforestry systems in different regions are highly variable, ranging from 0.59 to 11.08 t C · hm(-2) · a(-1), and it is mainly influenced by climatic factors and the characteristics of agroforestry systems (species composition, tree density and stand age). The soil C sequestration of any agroforestry system is influenced by the amount and quality of biomass input provided by tree and nontree components of the system and the soil properties such as soil texture and soil structure. Overall the amount of carbon storage in any agroforestry system depends on the structure and function of its each component. The future studies should focus on the carbon sink functions of structurally optimized agroforestry systems, the temporal variation and spatial distribution pattern of carbon storage in agroforestry system and its carbon sequestration mechanism in a long time.</p> </li> <li> <p><a target="_blank" rel="noopener noreferrer" onclick="trackOutboundLink('http://adsabs.harvard.edu/abs/2017AGUFMOS24A..01W','NASAADS'); return false;" href="http://adsabs.harvard.edu/abs/2017AGUFMOS24A..01W"><span>Resolving the Intricacies of Lateral Exports of Inorganic Carbon and Alkalinity from Coastal Salt Marshes</span></a></p> <p><a target="_blank" rel="noopener noreferrer" href="http://adsabs.harvard.edu/abstract_service.html">NASA Astrophysics Data System (ADS)</a></p> <p>Wang, A. Z.; Chu, S. N.; Kroeger, K. D.; Gonneea, M. E.; Ganju, N. K.</p> <p>2017-12-01</p> <p>Dynamic lateral exports of dissolved inorganic carbon (DIC) and total alkalinity (Alk) via tidal exchange from highly productive intertidal marshes are an important piece of puzzle in the coastal carbon cycle, challenging our capability of assessing coastal carbon budgets and projecting future changes under anthropogenic pressure. The effects of these exports on seawater chemistry are profound yet complicated to study. This study presents the latest development of assessing lateral DIC and Alk fluxes from tidal marshes and examining their effects on seawater chemistry and coastal carbon budgets. The study evaluates different approaches to quantify these exports in order to obtain insights on the best and efficient way to capture the dynamics of such exports. A state-of-the-art DIC sensor, Channelized Optical System (CHANOS), was deployed to establish the true DIC fluxes. They are compared to the fluxes derived from empirical modeling and traditional bottle measurements. Salt marshes can acidify and alkalize tidal water by injecting CO2 (DIC) and Alk over a same tidal cycle. However, their generation is decoupled as a result of deferential effects of aerobic and anaerobic respirations. This creates complex scenarios of large swings of seawater chemistry and buffering capacity in tidal water over tidal and seasonal cycles. Marsh exports of DIC and Alk may have complex implications for the future, more acidified ocean. The latest estimates of marsh DIC and Alk exports suggest they are a major term in the marsh carbon budget and can be translated into one of the primary components in the coastal carbon cycle.</p> </li> </ol> <div class="pull-right"> <ul class="pagination"> <li><a href="#" onclick='return showDiv("page_1");'>«</a></li> <li><a href="#" onclick='return showDiv("page_4");'>4</a></li> <li><a href="#" onclick='return showDiv("page_5");'>5</a></li> <li class="active"><span>6</span></li> <li><a href="#" onclick='return showDiv("page_7");'>7</a></li> <li><a href="#" onclick='return showDiv("page_8");'>8</a></li> <li><a href="#" onclick='return showDiv("page_25");'>»</a></li> </ul> </div> </div><!-- col-sm-12 --> </div><!-- row --> </div><!-- page_6 --> <div id="page_7" class="hiddenDiv"> <div class="row"> <div class="col-sm-12"> <div class="pull-right"> <ul class="pagination"> <li><a href="#" onclick='return showDiv("page_1");'>«</a></li> <li><a href="#" onclick='return showDiv("page_5");'>5</a></li> <li><a href="#" onclick='return showDiv("page_6");'>6</a></li> <li class="active"><span>7</span></li> <li><a href="#" onclick='return showDiv("page_8");'>8</a></li> <li><a href="#" onclick='return showDiv("page_9");'>9</a></li> <li><a href="#" onclick='return showDiv("page_25");'>»</a></li> </ul> </div> </div> </div> <div class="row"> <div class="col-sm-12"> <ol class="result-class" start="121"> <li> <p><a target="_blank" rel="noopener noreferrer" onclick="trackOutboundLink('https://www.ncbi.nlm.nih.gov/pubmed/24156818','PUBMED'); return false;" href="https://www.ncbi.nlm.nih.gov/pubmed/24156818"><span>Real-time black carbon emission factor measurements from light duty vehicles.</span></a></p> <p><a target="_blank" rel="noopener noreferrer" href="https://www.ncbi.nlm.nih.gov/entrez/query.fcgi?DB=pubmed">PubMed</a></p> <p>Forestieri, Sara D; Collier, Sonya; Kuwayama, Toshihiro; Zhang, Qi; Kleeman, Michael J; Cappa, Christopher D</p> <p>2013-11-19</p> <p>Eight light-duty gasoline low emission vehicles (LEV I) were tested on a Chassis dynamometer using the California Unified Cycle (UC) at the Haagen-Smit vehicle test facility at the California Air Resources Board in El Monte, CA during September 2011. The UC includes a cold start phase followed by a hot stabilized running phase. In addition, a light-duty gasoline LEV vehicle and ultralow emission vehicle (ULEV), and a light-duty diesel passenger vehicle and gasoline direct injection (GDI) vehicle were tested on a constant velocity driving cycle. A variety of instruments with response times ≥0.1 Hz were used to characterize how the emissions of the major particulate matter components varied for the LEVs during a typical driving cycle. This study focuses primarily on emissions of black carbon (BC). These measurements allowed for the determination of BC emission factors throughout the driving cycle, providing insights into the temporal variability of BC emission factors during different phases of a typical driving cycle.</p> </li> <li> <p><a target="_blank" rel="noopener noreferrer" onclick="trackOutboundLink('http://adsabs.harvard.edu/abs/2012AGUFM.B31B0423W','NASAADS'); return false;" href="http://adsabs.harvard.edu/abs/2012AGUFM.B31B0423W"><span>Soil Carbon and Nitrogen Cycle Modeling</span></a></p> <p><a target="_blank" rel="noopener noreferrer" href="http://adsabs.harvard.edu/abstract_service.html">NASA Astrophysics Data System (ADS)</a></p> <p>Woo, D.; Chaoka, S.; Kumar, P.; Quijano, J. C.</p> <p>2012-12-01</p> <p>Second generation bioenergy crops, such as miscanthus (Miscantus × giganteus) and switchgrass (Panicum virgatum), are regarded as clean energy sources, and are an attractive option to mitigate the human-induced climate change. However, the global climate change and the expansion of perennial grass bioenergy crops have the power to alter the biogeochemical cycles in soil, especially, soil carbon storages, over long time scales. In order to develop a predictive understanding, this study develops a coupled hydrological-soil nutrient model to simulate soil carbon responses under different climate scenarios such as: (i) current weather condition, (ii) decreased precipitation by -15%, and (iii) increased temperature up to +3C for four different crops, namely miscanthus, switchgrass, maize, and natural prairie. We use Precision Agricultural Landscape Modeling System (PALMS), version 5.4.0, to capture biophysical and hydrological components coupled with a multilayer carbon and ¬nitrogen cycle model. We apply the model at daily time scale to the Energy Biosciences Institute study site, located in the University of Illinois Research Farms, in Urbana, Illinois. The atmospheric forcing used to run the model was generated stochastically from parameters obtained using available data recorded in Bondville Ameriflux Site. The model simulations are validated with observations of drainage and nitrate and ammonium concentrations recorded in drain tiles during 2011. The results of this study show (1) total soil carbon storage of miscanthus accumulates most noticeably due to the significant amount of aboveground plant carbon, and a relatively high carbon to nitrogen ratio and lignin content, which reduce the litter decomposition rate. Also, (2) the decreased precipitation contributes to the enhancement of total soil carbon storage and soil nitrogen concentration because of the reduced microbial biomass pool. However, (3) an opposite effect on the cycle is introduced by the increased temperature. The simulation results obtained in this study show differences in the soil biogeochemistry induced by the different crops analyzed. Considering the spatial scale at which this crops are cultivated this results suggest there could be important implications in the carbon and nitrogen cycle and indirect feedbacks on climate change. This study also helps us understand the future soil mineral cycle, and ensure a sustainable transition to bioenergy crops.</p> </li> <li> <p><a target="_blank" rel="noopener noreferrer" onclick="trackOutboundLink('https://www.pubmedcentral.nih.gov/articlerender.fcgi?tool=pmcentrez&artid=5087067','PMC'); return false;" href="https://www.pubmedcentral.nih.gov/articlerender.fcgi?tool=pmcentrez&artid=5087067"><span>Thermogenic methane release as a cause for the long duration of the PETM</span></a></p> <p><a target="_blank" rel="noopener noreferrer" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?DB=pmc">PubMed Central</a></p> <p>Frieling, Joost; Svensen, Henrik H.; Planke, Sverre; Cramwinckel, Margot J.; Selnes, Haavard; Sluijs, Appy</p> <p>2016-01-01</p> <p>The Paleocene–Eocene Thermal Maximum (PETM) (∼56 Ma) was a ∼170,000-y (∼170-kyr) period of global warming associated with rapid and massive injections of 13C-depleted carbon into the ocean–atmosphere system, reflected in sedimentary components as a negative carbon isotope excursion (CIE). Carbon cycle modeling has indicated that the shape and magnitude of this CIE are generally explained by a large and rapid initial pulse, followed by ∼50 kyr of 13C-depleted carbon injection. Suggested sources include submarine methane hydrates, terrigenous organic matter, and thermogenic methane and CO2 from hydrothermal vent complexes. Here, we test for the contribution of carbon release associated with volcanic intrusions in the North Atlantic Igneous Province. We use dinoflagellate cyst and stable carbon isotope stratigraphy to date the active phase of a hydrothermal vent system and find it to postdate massive carbon release at the onset of the PETM. Crucially, however, it correlates to the period within the PETM of longer-term 13C-depleted carbon release. This finding represents actual proof of PETM carbon release from a particular reservoir. Based on carbon cycle box model [i.e., Long-Term Ocean–Atmosphere–Sediment Carbon Cycle Reservoir (LOSCAR) model] experiments, we show that 4–12 pulses of carbon input from vent systems over 60 kyr with a total mass of 1,500 Pg of C, consistent with the vent literature, match the shape of the CIE and pattern of deep ocean carbonate dissolution as recorded in sediment records. We therefore conclude that CH4 from the Norwegian Sea vent complexes was likely the main source of carbon during the PETM, following its dramatic onset. PMID:27790990</p> </li> <li> <p><a target="_blank" rel="noopener noreferrer" onclick="trackOutboundLink('http://adsabs.harvard.edu/abs/2017AGUFMGC21F0996B','NASAADS'); return false;" href="http://adsabs.harvard.edu/abs/2017AGUFMGC21F0996B"><span>Upscaling Ameriflux observations to assess drought impacts on gross primary productivity across the Southwest</span></a></p> <p><a target="_blank" rel="noopener noreferrer" href="http://adsabs.harvard.edu/abstract_service.html">NASA Astrophysics Data System (ADS)</a></p> <p>Barnes, M.; Moore, D. J.; Scott, R. L.; MacBean, N.; Ponce-Campos, G. E.; Breshears, D. D.</p> <p>2017-12-01</p> <p>Both satellite observations and eddy covariance estimates provide crucial information about the Earth's carbon, water and energy cycles. Continuous measurements from flux towers facilitate exploration of the exchange of carbon dioxide, water and energy between the land surface and the atmosphere at fine temporal and spatial scales, while satellite observations can fill in the large spatial gaps of in-situ measurements and provide long-term temporal continuity. The Southwest (Southwest United States and Northwest Mexico) and other semi-arid regions represent a key uncertainty in interannual variability in carbon uptake. Comparisons of existing global upscaled gross primary production (GPP) products with flux tower data at sites across the Southwest show widespread mischaracterization of seasonality in vegetation carbon uptake, resulting in large (up to 200%) errors in annual carbon uptake estimates. Here, remotely sensed and distributed meteorological inputs are used to upscale GPP estimates from 25 Ameriflux towers across the Southwest to the regional scale using a machine learning approach. Our random forest model incorporates two novel features that improve the spatial and temporal variability in GPP. First, we incorporate a multi-scalar drought index at multiple timescales to account for differential seasonality between ecosystem types. Second, our machine learning algorithm was trained on twenty five ecologically diverse sites to optimize both the monthly variability in and the seasonal cycle of GPP. The product and its components will be used to examine drought impacts on terrestrial carbon cycling across the Southwest including the effects of drought seasonality and on carbon uptake. Our spatially and temporally continuous upscaled GPP product drawing from both ground and satellite data over the Southwest region helps us understand linkages between the carbon and water cycles in semi-arid ecosystems and informs predictions of vegetation response to future climate conditions.</p> </li> <li> <p><a target="_blank" rel="noopener noreferrer" onclick="trackOutboundLink('http://adsabs.harvard.edu/abs/2005Natur.437..349A','NASAADS'); return false;" href="http://adsabs.harvard.edu/abs/2005Natur.437..349A"><span>Marine microorganisms and global nutrient cycles</span></a></p> <p><a target="_blank" rel="noopener noreferrer" href="http://adsabs.harvard.edu/abstract_service.html">NASA Astrophysics Data System (ADS)</a></p> <p>Arrigo, Kevin R.</p> <p>2005-09-01</p> <p>The way that nutrients cycle through atmospheric, terrestrial, oceanic and associated biotic reservoirs can constrain rates of biological production and help structure ecosystems on land and in the sea. On a global scale, cycling of nutrients also affects the concentration of atmospheric carbon dioxide. Because of their capacity for rapid growth, marine microorganisms are a major component of global nutrient cycles. Understanding what controls their distributions and their diverse suite of nutrient transformations is a major challenge facing contemporary biological oceanographers. What is emerging is an appreciation of the previously unknown degree of complexity within the marine microbial community.</p> </li> <li> <p><a target="_blank" rel="noopener noreferrer" onclick="trackOutboundLink('https://www.fs.usda.gov/treesearch/pubs/48146','TREESEARCH'); return false;" href="https://www.fs.usda.gov/treesearch/pubs/48146"><span>The importance of amino sugar turnover to C and N cycling in organic horizons of old-growth Douglas-fir forest soils colonized by ectomycorrhizal mats</span></a></p> <p><a target="_blank" rel="noopener noreferrer" href="http://www.fs.usda.gov/treesearch/">Treesearch</a></p> <p>L. Zeglin; L.A. Kluber; D.D. Myrold</p> <p>2012-01-01</p> <p>Amino sugar dynamics represent an important but under-investigated component of the carbon (C) and nitrogen (N) cycles in old-growth Douglas-fir forest soils. Because fungal biomass is high in these soils, particularly in areas colonized by rhizomorphic ectomycorrhizal fungal mats, organic matter derived from chitinous cell wall material (or the monomeric building...</p> </li> <li> <p><a target="_blank" rel="noopener noreferrer" onclick="trackOutboundLink('https://www.osti.gov/servlets/purl/1226230','DOE-PATENT-XML'); return false;" href="https://www.osti.gov/servlets/purl/1226230"><span>High capacity anode materials for lithium ion batteries</span></a></p> <p><a target="_blank" rel="noopener noreferrer" href="http://www.osti.gov/doepatents">DOEpatents</a></p> <p>Lopez, Herman A.; Anguchamy, Yogesh Kumar; Deng, Haixia; Han, Yongbon; Masarapu, Charan; Venkatachalam, Subramanian; Kumar, Suject</p> <p>2015-11-19</p> <p>High capacity silicon based anode active materials are described for lithium ion batteries. These materials are shown to be effective in combination with high capacity lithium rich cathode active materials. Supplemental lithium is shown to improve the cycling performance and reduce irreversible capacity loss for at least certain silicon based active materials. In particular silicon based active materials can be formed in composites with electrically conductive coatings, such as pyrolytic carbon coatings or metal coatings, and composites can also be formed with other electrically conductive carbon components, such as carbon nanofibers and carbon nanoparticles. Additional alloys with silicon are explored.</p> </li> <li> <p><a target="_blank" rel="noopener noreferrer" onclick="trackOutboundLink('https://ntrs.nasa.gov/search.jsp?R=20090005246&hterms=cycling&qs=Ntx%3Dmode%2Bmatchall%26Ntk%3DTitle%26N%3D0%26No%3D20%26Ntt%3Dcycling','NASA-TRS'); return false;" href="https://ntrs.nasa.gov/search.jsp?R=20090005246&hterms=cycling&qs=Ntx%3Dmode%2Bmatchall%26Ntk%3DTitle%26N%3D0%26No%3D20%26Ntt%3Dcycling"><span>U.S. Eastern Continental Shelf Carbon Cycling (USECoS): Modeling, Data Assimilation, and Analysis</span></a></p> <p><a target="_blank" rel="noopener noreferrer" href="http://ntrs.nasa.gov/search.jsp">NASA Technical Reports Server (NTRS)</a></p> <p>Mannino, Antonio</p> <p>2008-01-01</p> <p>Although the oceans play a major role in the uptake of fossil fuel CO2 from the atmosphere, there is much debate about the contribution from continental shelves, since many key shelf fluxes are not yet well quantified: the exchange of carbon across the land-ocean and shelf-slope interfaces, air-sea exchange of CO2, burial, and biological processes including productivity. Our goal is to quantify these carbon fluxes along the eastern U.S. coast using models quantitatively verified by comparison to observations, and to establish a framework for predicting how these fluxes may be modified as a result of climate and land use change. Our research questions build on those addressed with previous NASA funding for the USECoS (U.S. Eastern Continental Shelf Carbon Cycling) project. We have developed a coupled biogeochemical ocean circulation model configured for this study region and have extensively evaluated this model with both in situ and remotely-sensed data. Results indicate that to further reduce uncertainties in the shelf component of the global carbon cycle, future efforts must be directed towards 1) increasing the resolution of the physical model via nesting and 2) making refinements to the biogeochemical model and quantitatively evaluating these via the assimilation of biogeochemical data (in situ and remotely-sensed). These model improvements are essential for better understanding and reducing estimates of uncertainties in current and future carbon transformations and cycling in continental shelf systems. Our approach and science questions are particularly germane to the carbon cycle science goals of the NASA Earth Science Research Program as well as the U.S. Climate Change Research Program and the North American Carbon Program. Our interdisciplinary research team consists of scientists who have expertise in the physics and biogeochemistry of the U.S. eastern continental shelf, remote-sensing data analysis and data assimilative numerical models.</p> </li> <li> <p><a target="_blank" rel="noopener noreferrer" onclick="trackOutboundLink('https://www.fs.usda.gov/treesearch/pubs/53668','TREESEARCH'); return false;" href="https://www.fs.usda.gov/treesearch/pubs/53668"><span>Estimating belowground carbon stocks in peatlands of the Ecuadorian páramo using ground-penetrating radar (GPR)</span></a></p> <p><a target="_blank" rel="noopener noreferrer" href="http://www.fs.usda.gov/treesearch/">Treesearch</a></p> <p>Xavier Comas; Neil Terry; John A. Hribljan; Erik A. Lilleskov; Esteban Suarez; Rodney A. Chimner; Randy K. Kolka</p> <p>2017-01-01</p> <p>The páramo ecoregion of Ecuador contains extensive peatlands that are known to contain carbon (C) dense soils capable of long-term C storage. Although high-altitude mountain peatlands are typically small when compared to low-altitude peatlands, they are abundant across the Andean landscape and are likely a key component in regional C cycling. Since efforts to quantify...</p> </li> <li> <p><a target="_blank" rel="noopener noreferrer" onclick="trackOutboundLink('http://adsabs.harvard.edu/abs/2018JPS...384..328S','NASAADS'); return false;" href="http://adsabs.harvard.edu/abs/2018JPS...384..328S"><span>A high-performance ternary Si composite anode material with crystal graphite core and amorphous carbon shell</span></a></p> <p><a target="_blank" rel="noopener noreferrer" href="http://adsabs.harvard.edu/abstract_service.html">NASA Astrophysics Data System (ADS)</a></p> <p>Sui, Dong; Xie, Yuqing; Zhao, Weimin; Zhang, Hongtao; Zhou, Ying; Qin, Xiting; Ma, Yanfeng; Yang, Yong; Chen, Yongsheng</p> <p>2018-04-01</p> <p>Si is a promising anode material for lithium-ion batteries, but suffers from sophisticated engineering structures and complex fabrication processes that pose challenges for commercial application. Herein, a ternary Si/graphite/pyrolytic carbon (SiGC) anode material with a structure of crystal core and amorphous shell using low-cost raw materials is developed. In this ternary SiGC composite, Si component exists as nanoparticles and is spread on the surface of the core graphite flakes while the sucrose-derived pyrolytic carbon further covers the graphite/Si components as the amorphous shell. With this structure, Si together with the graphite contributes to the high specific capacity of this Si ternary material. Also the graphite serves as the supporting and conducting matrix and the amorphous shell carbon could accommodate the volume change effect of Si, reinforces the integrity of the composite architecture, and prevents the graphite and Si from direct exposing to the electrolyte. The optimized ternary SiGC composite displays high reversible specific capacity of 818 mAh g-1 at 0.1 A g-1, initial Coulombic efficiency (CE) over 80%, and excellent cycling stability at 0.5 A g-1 with 83.6% capacity retention (∼610 mAh g-1) after 300 cycles.</p> </li> <li> <p><a target="_blank" rel="noopener noreferrer" onclick="trackOutboundLink('http://adsabs.harvard.edu/abs/2015GGG....16.3383D','NASAADS'); return false;" href="http://adsabs.harvard.edu/abs/2015GGG....16.3383D"><span>Glacioeustasy, meteoric diagenesis, and the carbon cycle during the Middle Carboniferous</span></a></p> <p><a target="_blank" rel="noopener noreferrer" href="http://adsabs.harvard.edu/abstract_service.html">NASA Astrophysics Data System (ADS)</a></p> <p>Dyer, Blake; Maloof, Adam C.; Higgins, John A.</p> <p>2015-10-01</p> <p>Middle Carboniferous carbonates in the western U.S. have undergone Pleistocene Bahamas-style meteoric diagenesis that may be associated with expanding late Paleozoic ice sheets. Fourteen stratigraphic sections from carbonate platforms illustrate the regional distribution and variable intensity of physical and chemical diagenesis just below the Middle Carboniferous unconformity. These sections contain top-negative carbon isotope excursions that terminate in regional exposure surfaces that are associated with some combination of karst towers, desiccation cracks, fabric destructive recrystallization, or extensive root systems. The timing of the diagenesis is synchronous with similarly scaled top-negative carbon isotope excursions observed by others in England, Kazakhstan, and China. The mass flux of negative carbon required to generate similar isotopic profiles across the areal extent of Middle Carboniferous platform carbonates is a significant component of the global carbon cycle. We present a simple carbon box model to illustrate that the δ13C of dissolved inorganic carbon in the ocean could be elevated by ˜1.4‰ as isotopically light carbon from the weathering of terrestrial organic matter reacts with exposed platforms before reaching the ocean and atmosphere. These results represent an improvement on global biogeochemical models that have struggled to provide a congruent solution to the high δ13C of the late Paleozoic icehouse.</p> </li> <li> <p><a target="_blank" rel="noopener noreferrer" onclick="trackOutboundLink('http://adsabs.harvard.edu/abs/2014JPS...267..812L','NASAADS'); return false;" href="http://adsabs.harvard.edu/abs/2014JPS...267..812L"><span>Synthesis of three-dimensionally ordered macroporous manganese dioxide-carbon nanocomposites for supercapacitors</span></a></p> <p><a target="_blank" rel="noopener noreferrer" href="http://adsabs.harvard.edu/abstract_service.html">NASA Astrophysics Data System (ADS)</a></p> <p>Liu, Zhi; Tan, Xiuli; Gao, Xin; Song, Lihong</p> <p>2014-12-01</p> <p>In this article, we report a composite of MnO2 nanoparticles supported by three-dimensionally ordered macroporous carbon (MnO2/3DOM carbon nanocomposites) fabricated by means of a simple multi-component infiltration of three-dimensional templates. MnO2 nanoparticles of 2 nm-6 nm are observed to be highly dispersed on the 3DOM carbon scaffolds. Cyclic voltammetry, galvanostatic charge/discharge and electrochemical impedance spectroscopy techniques are employed to assess the properties of these nanocomposites for use in supercapacitors. The results demonstrate that MnO2 can be effectively utilized with assistance of the 3DOM carbon in the electrode. The specific capacitance of the nanocomposite electrode can reach as high as 347 F g-1 at a current density of 0.5 A g-1. Moreover, the electrode exhibit excellent charge/discharge rate and good cycling stability, retaining over 92% of its initial charge after 5500 cycles at a current density of 2.5 A g-1. Such MnO2/3DOM carbon nanocomposite represents a promising exploring direction for enhancing the device performance of metal oxide-based electrochemical supercapacitors.</p> </li> <li> <p><a target="_blank" rel="noopener noreferrer" onclick="trackOutboundLink('http://adsabs.harvard.edu/abs/2017EGUGA..1914645S','NASAADS'); return false;" href="http://adsabs.harvard.edu/abs/2017EGUGA..1914645S"><span>Estimating national forest carbon stocks and dynamics: combining models and remotely sensed information</span></a></p> <p><a target="_blank" rel="noopener noreferrer" href="http://adsabs.harvard.edu/abstract_service.html">NASA Astrophysics Data System (ADS)</a></p> <p>Smallman, Thomas Luke; Exbrayat, Jean-François; Bloom, Anthony; Williams, Mathew</p> <p>2017-04-01</p> <p>Forests are a critical component of the global carbon cycle, storing significant amounts of carbon, split between living biomass and dead organic matter. The carbon budget of forests is the most uncertain component of the global carbon cycle - it is currently impossible to quantify accurately the carbon source/sink strength of forest biomes due to their heterogeneity and complex dynamics. It has been a major challenge to generate robust carbon budgets across landscapes due to data scarcity. Models have been used for estimating carbon budgets, but outputs have lacked an assessment of uncertainty, making a robust assessment of their reliability and accuracy challenging. Here a Metropolis Hastings - Markov Chain Monte Carlo (MH-MCMC) data assimilation framework has been used to combine remotely sensed leaf area index (MODIS), biomass (where available) and deforestation estimates, in addition to forest planting information from the UK's national forest inventory, an estimate of soil carbon from the Harmonized World Database (HWSD) and plant trait information with a process model (DALEC) to produce a constrained analysis with a robust estimate of uncertainty of the UK forestry carbon budget between 2000 and 2010. Our analysis estimates the mean annual UK forest carbon sink at -3.9 MgC ha-1 yr-1 with a 95 % confidence interval between -4.0 and -3.1 MgC ha-1yr-1. The UK national forest inventory (NFI) estimates the mean UK forest carbon sink to be between -1.4 and -5.5 MgC ha-1 yr-1. The analysis estimate for total forest biomass stock in 2010 is estimated at 229 (177/232) TgC, while the NFI an estimated total forest biomass carbon stock of 216 TgC. Leaf carbon area (LCA) is a key plant trait which we are able to estimate using our analysis. Comparison of median estimates for (LCA) retrieved from the analysis and a UK land cover map show higher and lower values for LCA are estimated areas dominated by needle leaf and broad leaf forests forest respectively, consistent with ecological expectations. Moreover, LCA is positively and negatively correlated with leaf-life span and allocation of photosynthate to foliage respectively, supported by field observations. This emergence of key plant traits and correlations between traits increases our confidence in the robustness of this analysis. Furthermore, this framework also allows us to search for additional emergent properties from the analysis such as spatial variation of retrieved drought tolerance. Finally our analysis is able to identify components of the carbon cycle with the largest uncertainty e.g. allocation of photosynthate to wood and wood residence times, providing targets for future observations (e.g. ESA's BIOMASS mission). Our Bayesian analysis system is ideally suited for assimilation of multiple biomass estimates and their associated uncertainties to reduce both the overall analysis uncertainty and bias in estimates biomass stocks.</p> </li> <li> <p><a target="_blank" rel="noopener noreferrer" onclick="trackOutboundLink('https://www.ncbi.nlm.nih.gov/pubmed/22628557','PUBMED'); return false;" href="https://www.ncbi.nlm.nih.gov/pubmed/22628557"><span>A reduced organic carbon component in martian basalts.</span></a></p> <p><a target="_blank" rel="noopener noreferrer" href="https://www.ncbi.nlm.nih.gov/entrez/query.fcgi?DB=pubmed">PubMed</a></p> <p>Steele, A; McCubbin, F M; Fries, M; Kater, L; Boctor, N Z; Fogel, M L; Conrad, P G; Glamoclija, M; Spencer, M; Morrow, A L; Hammond, M R; Zare, R N; Vicenzi, E P; Siljeström, S; Bowden, R; Herd, C D K; Mysen, B O; Shirey, S B; Amundsen, H E F; Treiman, A H; Bullock, E S; Jull, A J T</p> <p>2012-07-13</p> <p>The source and nature of carbon on Mars have been a subject of intense speculation. We report the results of confocal Raman imaging spectroscopy on 11 martian meteorites, spanning about 4.2 billion years of martian history. Ten of the meteorites contain abiotic macromolecular carbon (MMC) phases detected in association with small oxide grains included within high-temperature minerals. Polycyclic aromatic hydrocarbons were detected along with MMC phases in Dar al Gani 476. The association of organic carbon within magmatic minerals indicates that martian magmas favored precipitation of reduced carbon species during crystallization. The ubiquitous distribution of abiotic organic carbon in martian igneous rocks is important for understanding the martian carbon cycle and has implications for future missions to detect possible past martian life.</p> </li> <li> <p><a target="_blank" rel="noopener noreferrer" onclick="trackOutboundLink('http://adsabs.harvard.edu/abs/2013JPS...243..880H','NASAADS'); return false;" href="http://adsabs.harvard.edu/abs/2013JPS...243..880H"><span>Supercapacitors based on 3D network of activated carbon nanowhiskers wrapped-on graphitized electrospun nanofibers</span></a></p> <p><a target="_blank" rel="noopener noreferrer" href="http://adsabs.harvard.edu/abstract_service.html">NASA Astrophysics Data System (ADS)</a></p> <p>He, Shuijian; Chen, Linlin; Xie, Chencheng; Hu, Huan; Chen, Shuiliang; Hanif, Muddasir; Hou, Haoqing</p> <p>2013-12-01</p> <p>Due to their cycling stability and high power density, the supercapacitors bridge the power/energy gap between traditional dielectric capacitors and batteries/fuel cells. Electrode materials are key components for making high performance supercapacitors. An activated carbon nanowhiskers (ACNWs) wrapped-on graphitized electrospun nanofiber (GENF) network (ACNWs/GENFN) with 3D porous structure is prepared as a new type of binder-free electrode material for supercapacitors. The supercapacitor based on the ACNWs/GENFN composite material displays an excellent performance with a specific capacitance of 176.5 F g-1 at current density of 0.5 A g-1, an ultrahigh power density of 252.8 kW kg-1 at current density of 800 A g-1 and an outstanding cycling stability of no capacitance loss after 10,000 charge/discharge cycles.</p> </li> <li> <p><a target="_blank" rel="noopener noreferrer" onclick="trackOutboundLink('https://www.ncbi.nlm.nih.gov/pubmed/27714175','PUBMED'); return false;" href="https://www.ncbi.nlm.nih.gov/pubmed/27714175"><span>Inherent N,O-containing carbon frameworks as electrode materials for high-performance supercapacitors.</span></a></p> <p><a target="_blank" rel="noopener noreferrer" href="https://www.ncbi.nlm.nih.gov/entrez/query.fcgi?DB=pubmed">PubMed</a></p> <p>Hu, Fangyuan; Wang, Jinyan; Hu, Shui; Li, Linfei; Wang, Gang; Qiu, Jieshan; Jian, Xigao</p> <p>2016-09-15</p> <p>N,O-Containing micropore-dominated materials have been developed successfully via temperature-dependent cross-linking of 4,4'-(dioxo-diphenyl-2,3,6,7-tetraazaanthracenediyl)dibenzonitrile (DPDN) monomers. By employing a molecular engineering strategy, we have designed and synthesized a series of porous heteroatom-containing carbon frameworks (PHCFs), in which nitrogen and oxygen heteroatoms are distributed homogeneously throughout the whole framework at the atomic level, which can ensure the stability of its electrical properties. The as-made PHCFs@550 exhibits a high specific capacitance of 378 F g -1 , with an excellent long cycling life, including excellent cycling stability (capacitance retention of ca. 120% over 20 000 cycles). Moreover, the successful preparation of PHCFs provides new insights for the fabrication of nitrogen and oxygen-containing electrode materials from readily available components via a facile route.</p> </li> <li> <p><a target="_blank" rel="noopener noreferrer" onclick="trackOutboundLink('http://adsabs.harvard.edu/abs/2017JPhCS.821a2027R','NASAADS'); return false;" href="http://adsabs.harvard.edu/abs/2017JPhCS.821a2027R"><span>Preliminary design of a supercritical CO2 wind tunnel</span></a></p> <p><a target="_blank" rel="noopener noreferrer" href="http://adsabs.harvard.edu/abstract_service.html">NASA Astrophysics Data System (ADS)</a></p> <p>Re, B.; Rurale, A.; Spinelli, A.; Guardone, A.</p> <p>2017-03-01</p> <p>The preliminary design of a test-rig for non-ideal compressible-fluid flows of carbon dioxide is presented. The test-rig is conceived to investigate supersonic flows that are relevant to the study of non-ideal compressible-fluid flows in the close proximity of the critical point and of the liquid-vapor saturation curve, to the investigation of drop nucleation in compressors operating with supercritical carbon dioxide and and to the study of flow conditions similar to those encountered in turbines for Organic Rankine Cycle applications. Three different configurations are presented and examined: a batch-operating test-rig, a closed-loop Brayton cycle and a closed-loop Rankine cycle. The latter is preferred for its versatility and for economic reasons. A preliminary design of the main components is reported, including the heat exchangers, the chiller, the pumps and the test section.</p> </li> <li> <p><a target="_blank" rel="noopener noreferrer" onclick="trackOutboundLink('https://cfpub.epa.gov/si/si_public_record_report.cfm?dirEntryId=336401&Lab=NHEERL&keyword=system+AND+dynamics&actType=&TIMSType=+&TIMSSubTypeID=&DEID=&epaNumber=&ntisID=&archiveStatus=Both&ombCat=Any&dateBeginCreated=&dateEndCreated=&dateBeginPublishedPresented=&dateEndPublishedPresented=&dateBeginUpdated=&dateEndUpdated=&dateBeginCompleted=&dateEndCompleted=&personID=&role=Any&journalID=&publisherID=&sortBy=revisionDate&count=50','EPA-EIMS'); return false;" href="https://cfpub.epa.gov/si/si_public_record_report.cfm?dirEntryId=336401&Lab=NHEERL&keyword=system+AND+dynamics&actType=&TIMSType=+&TIMSSubTypeID=&DEID=&epaNumber=&ntisID=&archiveStatus=Both&ombCat=Any&dateBeginCreated=&dateEndCreated=&dateBeginPublishedPresented=&dateEndPublishedPresented=&dateBeginUpdated=&dateEndUpdated=&dateBeginCompleted=&dateEndCompleted=&personID=&role=Any&journalID=&publisherID=&sortBy=revisionDate&count=50"><span>The Freshwater Landscape: Lake, Wetland, and Stream Abundance and Connectivity at Macroscales</span></a></p> <p><a target="_blank" rel="noopener noreferrer" href="http://oaspub.epa.gov/eims/query.page">EPA Science Inventory</a></p> <p></p> <p></p> <p>It is becoming increasingly recognized that inland waterbodies and their surface hydrologic connections are active components in the landscape, influencing multiple ecological processes that can propagate to broad-scale phenomena such as regional nutrient and carbon cycles and me...</p> </li> <li> <p><a target="_blank" rel="noopener noreferrer" onclick="trackOutboundLink('https://www.ncbi.nlm.nih.gov/pubmed/26150108','PUBMED'); return false;" href="https://www.ncbi.nlm.nih.gov/pubmed/26150108"><span>Climate and landscape influence on indicators of lake carbon cycling through spatial patterns in dissolved organic carbon.</span></a></p> <p><a target="_blank" rel="noopener noreferrer" href="https://www.ncbi.nlm.nih.gov/entrez/query.fcgi?DB=pubmed">PubMed</a></p> <p>Lapierre, Jean-Francois; Seekell, David A; Del Giorgio, Paul A</p> <p>2015-12-01</p> <p>Freshwater ecosystems are strongly influenced by both climate and the surrounding landscape, yet the specific pathways connecting climatic and landscape drivers to the functioning of lake ecosystems are poorly understood. Here, we hypothesize that the links that exist between spatial patterns in climate and landscape properties and the spatial variation in lake carbon (C) cycling at regional scales are at least partly mediated by the movement of terrestrial dissolved organic carbon (DOC) in the aquatic component of the landscape. We assembled a set of indicators of lake C cycling (bacterial respiration and production, chlorophyll a, production to respiration ratio, and partial pressure of CO2 ), DOC concentration and composition, and landscape and climate characteristics for 239 temperate and boreal lakes spanning large environmental and geographic gradients across seven regions. There were various degrees of spatial structure in climate and landscape features that were coherent with the regionally structured patterns observed in lake DOC and indicators of C cycling. These different regions aligned well, albeit nonlinearly along a mean annual temperature gradient; whereas there was a considerable statistical effect of climate and landscape properties on lake C cycling, the direct effect was small and the overall effect was almost entirely overlapping with that of DOC concentration and composition. Our results suggest that key climatic and landscape signals are conveyed to lakes in part via the movement of terrestrial DOC to lakes and that DOC acts both as a driver of lake C cycling and as a proxy for other external signals. © 2015 John Wiley & Sons Ltd.</p> </li> <li> <p><a target="_blank" rel="noopener noreferrer" onclick="trackOutboundLink('http://adsabs.harvard.edu/abs/2004AGUFM.B24A..06B','NASAADS'); return false;" href="http://adsabs.harvard.edu/abs/2004AGUFM.B24A..06B"><span>Quantifying Sources and Fluxes of Aquatic Carbon in U.S. Streams and Reservoirs Using Spatially Referenced Regression Models</span></a></p> <p><a target="_blank" rel="noopener noreferrer" href="http://adsabs.harvard.edu/abstract_service.html">NASA Astrophysics Data System (ADS)</a></p> <p>Boyer, E. W.; Smith, R. A.; Alexander, R. B.; Schwarz, G. E.</p> <p>2004-12-01</p> <p>Organic carbon (OC) is a critical water quality characteristic in riverine systems that is an important component of the aquatic carbon cycle and energy balance. Examples of processes controlled by OC interactions are complexation of trace metals; enhancement of the solubility of hydrophobic organic contaminants; formation of trihalomethanes in drinking water; and absorption of visible and UV radiation. Organic carbon also can have indirect effects on water quality by influencing internal processes of aquatic ecosystems (e.g. photosynthesis and autotrophic and heterotrophic activity). The importance of organic matter dynamics on water quality has been recognized, but challenges remain in quantitatively addressing OC processes over broad spatial scales in a hydrological context. In this study, we apply spatially referenced watershed models (SPARROW) to statistically estimate long-term mean-annual rates of dissolved- and total- organic carbon export in streams and reservoirs across the conterminous United States. We make use of a GIS framework for the analysis, describing sources, transport, and transformations of organic matter from spatial databases providing characterizations of climate, land use, primary productivity, topography, soils, and geology. This approach is useful because it illustrates spatial patterns of organic carbon fluxes in streamflow, highlighting hot spots (e.g., organic-rich environments in the southeastern coastal plain). Further, our simulations provide estimates of the relative contributions to streams from allochthonous and autochthonous sources. We quantify surface water fluxes of OC with estimates of uncertainty in relation to the overall US carbon budget; our simulations highlight that aquatic sources and sinks of OC may be a more significant component of regional carbon cycling than was previously thought. Further, we are using our simulations to explore the potential role of climate and other changes in the terrestrial environment on OC fluxes in aquatic systems.</p> </li> </ol> <div class="pull-right"> <ul class="pagination"> <li><a href="#" onclick='return showDiv("page_1");'>«</a></li> <li><a href="#" onclick='return showDiv("page_5");'>5</a></li> <li><a href="#" onclick='return showDiv("page_6");'>6</a></li> <li class="active"><span>7</span></li> <li><a href="#" onclick='return showDiv("page_8");'>8</a></li> <li><a href="#" onclick='return showDiv("page_9");'>9</a></li> <li><a href="#" onclick='return showDiv("page_25");'>»</a></li> </ul> </div> </div><!-- col-sm-12 --> </div><!-- row --> </div><!-- page_7 --> <div id="page_8" class="hiddenDiv"> <div class="row"> <div class="col-sm-12"> <div class="pull-right"> <ul class="pagination"> <li><a href="#" onclick='return showDiv("page_1");'>«</a></li> <li><a href="#" onclick='return showDiv("page_6");'>6</a></li> <li><a href="#" onclick='return showDiv("page_7");'>7</a></li> <li class="active"><span>8</span></li> <li><a href="#" onclick='return showDiv("page_9");'>9</a></li> <li><a href="#" onclick='return showDiv("page_10");'>10</a></li> <li><a href="#" onclick='return showDiv("page_25");'>»</a></li> </ul> </div> </div> </div> <div class="row"> <div class="col-sm-12"> <ol class="result-class" start="141"> <li> <p><a target="_blank" rel="noopener noreferrer" onclick="trackOutboundLink('https://www.ncbi.nlm.nih.gov/pubmed/12460485','PUBMED'); return false;" href="https://www.ncbi.nlm.nih.gov/pubmed/12460485"><span>Forests, carbon and global climate.</span></a></p> <p><a target="_blank" rel="noopener noreferrer" href="https://www.ncbi.nlm.nih.gov/entrez/query.fcgi?DB=pubmed">PubMed</a></p> <p>Malhi, Yadvinder; Meir, Patrick; Brown, Sandra</p> <p>2002-08-15</p> <p>This review places into context the role that forest ecosystems play in the global carbon cycle, and their potential interactions with climate change. We first examine the natural, preindustrial carbon cycle. Every year forest gross photosynthesis cycles approximately one-twelfth of the atmospheric stock of carbon dioxide, accounting for 50% of terrestrial photosynthesis. This cycling has remained almost constant since the end of the last ice age, but since the Industrial Revolution it has undergone substantial disruption as a result of the injection of 480 PgC into the atmosphere through fossil-fuel combustion and land-use change, including forest clearance. In the second part of this paper we review this 'carbon disruption', and its impact on the oceans, atmosphere and biosphere. Tropical deforestation is resulting in a release of 1.7 PgC yr(-1) into the atmosphere. However, there is also strong evidence for a 'sink' for carbon in natural vegetation (carbon absorption), which can be explained partly by the regrowth of forests on abandoned lands, and partly by a global change factor, the most likely cause being 'fertilization' resulting from the increase in atmospheric CO(2). In the 1990s this biosphere sink was estimated to be sequestering 3.2 PgC yr(-1) and is likely to have substantial effects on the dynamics, structure and biodiversity of all forests. Finally, we examine the potential for forest protection and afforestation to mitigate climate change. An extensive global carbon sequestration programme has the potential to make a particularly significant contribution to controlling the rise in CO2 emissions in the next few decades. In the course of the whole century, however, even the maximum amount of carbon that could be sequestered will be dwarfed by the magnitude of (projected) fossil-fuel emissions. Forest carbon sequestration should only be viewed as a component of a mitigation strategy, not as a substitute for the changes in energy supply, use and technology that will be required if atmospheric CO(2) concentrations are to be stabilized.</p> </li> <li> <p><a target="_blank" rel="noopener noreferrer" onclick="trackOutboundLink('http://adsabs.harvard.edu/abs/2016EGUGA..18.3012S','NASAADS'); return false;" href="http://adsabs.harvard.edu/abs/2016EGUGA..18.3012S"><span>Estimating national forest carbon stocks and dynamics: combining models and remotely sensed information</span></a></p> <p><a target="_blank" rel="noopener noreferrer" href="http://adsabs.harvard.edu/abstract_service.html">NASA Astrophysics Data System (ADS)</a></p> <p>Smallman, Luke; Williams, Mathew</p> <p>2016-04-01</p> <p>Forests are a critical component of the global carbon cycle, storing significant amounts of carbon, split between living biomass and dead organic matter. The carbon budget of forests is the most uncertain component of the global carbon cycle - it is currently impossible to quantify accurately the carbon source/sink strength of forest biomes due to their heterogeneity and complex dynamics. It has been a major challenge to generate robust carbon budgets across landscapes due to data scarcity. Models have been used but outputs have lacked an assessment of uncertainty, making a robust assessment of their reliability and accuracy challenging. Here a Metropolis Hastings - Markov Chain Monte Carlo (MH-MCMC) data assimilation framework has been used to combine remotely sensed leaf area index (MODIS), biomass (where available) and deforestation estimates, in addition to forest planting and clear-felling information from the UK's national forest inventory, an estimate of soil carbon from the Harmonized World Database (HWSD) and plant trait information with a process model (DALEC) to produce a constrained analysis with a robust estimate of uncertainty of the UK forestry carbon budget between 2000 and 2010. Our analysis estimates the mean annual UK forest carbon sink at -3.9 MgC ha-1yr-1 with a 95 % confidence interval between -4.0 and -3.1 MgC ha-1 yr-1. The UK national forest inventory (NFI) estimates the mean UK forest carbon sink to be between -1.4 and -5.5 MgC ha-1 yr-1. The analysis estimate for total forest biomass stock in 2010 is estimated at 229 (177/232) TgC, while the NFI an estimated total forest biomass carbon stock of 216 TgC. Leaf carbon area (LCA) is a key plant trait which we are able to estimate using our analysis. Comparison of median estimates for LCA retrieved from the analysis and a UK land cover map show higher and lower values for LCA are estimated areas dominated by needle leaf and broad leaf forests forest respectively, consistent with ecological expectations. Moreover, the retrieved LCA is positively correlated with leaf-life span and negatively correlated with allocation of photosynthate to foliage, supported by field observations. This emergence of key plant traits and correlations between traits increases our confidence in the robustness of this analysis. Furthermore, this framework also allows us to search for additional emergent properties from the analysis such as spatial variation of retrieved drought tolerance. Finally our analysis is able to identify components of the carbon cycle with the largest uncertainty providing targets for future observations (e.g. remotely sensed biomass). Our Bayesian analysis system is ideally suited for assimilation of multiple biomass estimates and their associated uncertainties to reduce both uncertainty in the state of the system but also process parameters (e.g. wood residence time).</p> </li> <li> <p><a target="_blank" rel="noopener noreferrer" onclick="trackOutboundLink('http://adsabs.harvard.edu/abs/2017JOM....69i1513I','NASAADS'); return false;" href="http://adsabs.harvard.edu/abs/2017JOM....69i1513I"><span>Bio-Derived Hierarchical 3D Architecture from Seeds for Supercapacitor Application</span></a></p> <p><a target="_blank" rel="noopener noreferrer" href="http://adsabs.harvard.edu/abstract_service.html">NASA Astrophysics Data System (ADS)</a></p> <p>Intawin, Pratthana; Sayed, Farheen N.; Pengpat, Kamonpan; Joyner, Jarin; Tiwary, Chandra Sekhar; Ajayan, Pulickel M.</p> <p>2017-09-01</p> <p>The generation and storage of green energy (energy from abundant and nonfossil) is important for a sustainable and clean future. The electrode material in a supercapacitor is a major component. The properties of these materials depend on its inherent architecture and composition. Here, we have chosen sunflower seeds and pumpkin seeds with a completely different structure to obtain a carbonaceous product. The product obtained from sunflower seed carbon is a three-dimensional hierarchical macroporous carbon (SSC) composed of many granular nanocrystals of potassium magnesium phosphate dispersed in a matrix. Contrary to this, carbon from pumpkin seeds (PSC) is revealed to be a more rigid structure, with no porous or ordered morphology. The electrochemical supercapacitive behavior was assessed by cyclic voltammetry and galvanostatic charge-discharge tests. Electrochemical measurements showed that the SSC shows a high specific capacitance of 24.9 Fg-1 as compared with that obtained (2.46 Fg-1) for PSC with a cycling efficiency of 87% and 89%, respectively. On high-temperature cycling for 500 charge-discharge cycles at 0.1 Ag-1, an improved cycling efficiency of 100% and 98% for SSC and PSC, respectively, is observed.</p> </li> <li> <p><a target="_blank" rel="noopener noreferrer" onclick="trackOutboundLink('https://pubs.er.usgs.gov/publication/70042392','USGSPUBS'); return false;" href="https://pubs.er.usgs.gov/publication/70042392"><span>Biological and geochemical controls on diel dissolved inorganic carbon cycling in a low-order agricultural stream: implications for reach scales and beyond</span></a></p> <p><a target="_blank" rel="noopener noreferrer" href="http://pubs.er.usgs.gov/pubs/index.jsp?view=adv">USGS Publications Warehouse</a></p> <p>Tobias, Craig; Böhlke, John Karl</p> <p>2011-01-01</p> <p>Movement of dissolved inorganic carbon (DIC) through the hydrologic cycle is an important component of global carbon budgets, but there is considerable uncertainty about the controls of DIC transmission from landscapes to streams, and through river networks to the oceans. In this study, diel measurements of DIC, d13C-DIC, dissolved oxygen (O2), d18O-O2, alkalinity, pH, and other parameters were used to assess the relative magnitudes of biological and geochemical controls on DIC cycling and flux in a nutrient-rich, net autotrophic stream. Rates of photosynthesis (P), respiration (R), groundwater discharge, air–water exchange of CO2, and carbonate precipitation/dissolution were quantified through a time-stepping chemical/isotope (12C and 13C, 16O and 18O) mass balance model. Groundwater was the major source of DIC to the stream. Primary production and carbonate precipitation were equally important sinks for DIC removed from the water column. The stream was always super-saturated with respect to carbonate minerals, but carbonate precipitation occurred mainly during the day when P increased pH. We estimated more than half (possibly 90%) of the carbonate precipitated during the day was retained in the reach under steady baseflow conditions. The amount of DIC removed from the overlying water through carbonate precipitation was similar to the amount of DIC generated from R. Air–water exchange of CO2 was always from the stream to the atmosphere, but was the smallest component of the DIC budget. Overall, the in-stream DIC reactions reduced the amount of CO2 evasion and the downstream flux of groundwater-derived DIC by about half relative to a hypothetical scenario with groundwater discharge only. Other streams with similar characteristics are widely distributed in the major river basins of North America. Data from USGS water quality monitoring networks from the 1960s to the 1990s indicated that 40% of 652 stream monitoring stations in the contiguous USA were at or above the equilibrium saturation state for calcite, and 77% of all stations exhibited apparent increases in saturation state from the 1960/70s to the 1980/90s. Diel processes including partially irreversible carbonate precipitation may affect net carbon fluxes from many such watersheds</p> </li> <li> <p><a target="_blank" rel="noopener noreferrer" onclick="trackOutboundLink('http://adsabs.harvard.edu/abs/2009AGUFM.V13G..01T','NASAADS'); return false;" href="http://adsabs.harvard.edu/abs/2009AGUFM.V13G..01T"><span>Long Term δ17O, δ18O measurements of tropospheric carbon dioxide and potential application to the global carbon cycle. (Invited)</span></a></p> <p><a target="_blank" rel="noopener noreferrer" href="http://adsabs.harvard.edu/abstract_service.html">NASA Astrophysics Data System (ADS)</a></p> <p>Thiemens, M. H.</p> <p>2009-12-01</p> <p>Stable isotope ratio measurements have played an important role in defining the global carbon cycle for the past half century. In the past decades, mass independent isotopic measurements of stratospheric carbon dioxide have been shown to be an important indice for understanding stratospheric ozone chemistry and the interaction with carbon dioxide. In this specific role, it is the O(1D) produced from ozone photolysis that interacts with CO2 and inscribes a mass independent isotopic composition (see review by (1)). This photochemical process simultaneously provides an isotopic record in carbon dioxide of the integrated exposure to ozone/atomic oxygen and stratosphere troposphere mixing. As a consequence of these processes, it has been observed that tropospheric oxygen possesses a mass independent composition that may be used as a tracer of bioproductivity (2) and as a potential measure of carbon dioxide levels during and following the snowball earth event (3). In addition, the magnitude of the stratospheric anomaly in the troposphere may directly reflect the atmospheric turnover rates of carbon dioxide, which is an important component of the carbon cycle (4, 5). To further develop this new methodology, the rates and magnitude of the relevant processes must be identified and quantified. Samples of tropospheric carbon dioxide were obtained in La Jolla, Ca. over a 10 year plus time period. All samples were taken under identical conditions and analyzed immediately for all three oxygen isotopes. There was no sample storage and samples were thoroughly isolated from water. All conditions, including standardization and mass spectrometry were constant throughout that time period. The data are consistent with an identifiable steady state component of stratospheric carbon dioxide. In addition, other features of the data suggest other processes operative that are presently unaccounted for, and, are only observable in the mass independent composition. References 1. Thiemens, M.H. (2006). Annual Rev. earth Planet Sci. 34, 217 (2006). 2.Luz, B., Bender, M.L., Thiemens, M.H., Boering, K. Nature 400, 547 (2002). 3.Bao, H., Lyons, J.R., Zhou, Chuanming. Nature 453, 504 (2008). 4.Hoag, K.J., Still, C.J., Fung, I.Y., Boering, K.A. Geophys. Res. Lett 32, L02802 (2005). 5.Liang, M-C., Blake, G.A., Yung, Y.L. J. Geophys. Res 113, D12305 (2008).</p> </li> <li> <p><a target="_blank" rel="noopener noreferrer" onclick="trackOutboundLink('http://adsabs.harvard.edu/abs/2010BGD.....7.3735F','NASAADS'); return false;" href="http://adsabs.harvard.edu/abs/2010BGD.....7.3735F"><span>Comprehensive description of the carbon cycle of an ancient temperate broadleaved woodland</span></a></p> <p><a target="_blank" rel="noopener noreferrer" href="http://adsabs.harvard.edu/abstract_service.html">NASA Astrophysics Data System (ADS)</a></p> <p>Fenn, K.; Malhi, Y.; Morecroft, M.; Lloyd, C.; Thomas, M.</p> <p>2010-05-01</p> <p>There exist very few comprehensive descriptions of the productivity and carbon cycling of forest ecosystems. Here we present a description of the components of annual Net Primary Productivity (NPP), Gross Primary Productivity (GPP), autotrophic and heterotrophic respiration, and ecosystem respiration (RECO) for a temperate mixed deciduous woodland at Wytham Woods in southern Britain, calculated using "bottom-up" biometric and chamber measurements (leaf and wood production and soil and stem respiration). These are compared with estimates of these parameters from eddy-covariance measurements made at the same site. NPP was estimated as 7.0±0.8 Mg C ha-1 yr-1, and GPP as 20.3+1.0 Mg C ha-1 yr-1, a value which closely matched to eddy covariance-derived GPP value of 21.1 Mg C ha-1 yr-1. Annual RECO was calculated as 18.9±1.7 Mg C ha-1 yr-1, close to the eddy covariance value of 19.8 Mg C ha-1 yr-1; the seasonal cycle of biometric and eddy covariance RECO estimates also closely matched. The consistency between eddy covariance and biometric measurements substantially strengthens the confidence we attach to each as alternative indicators of site carbon dynamics, and permits an integrated perspective of the ecosystem carbon cycle. 37% of NPP was allocated below ground, and the ecosystem carbon use efficiency (CUE, = NPP/GPP) calculated to be 0.35±0.05, lower than reported for many temperate broadleaved sites.</p> </li> <li> <p><a target="_blank" rel="noopener noreferrer" onclick="trackOutboundLink('https://www.osti.gov/biblio/1406778-pyhector-python-interface-simple-climate-model-hector','SCIGOV-STC'); return false;" href="https://www.osti.gov/biblio/1406778-pyhector-python-interface-simple-climate-model-hector"><span>pyhector: A Python interface for the simple climate model Hector</span></a></p> <p><a target="_blank" rel="noopener noreferrer" href="http://www.osti.gov/search">DOE Office of Scientific and Technical Information (OSTI.GOV)</a></p> <p>N Willner, Sven; Hartin, Corinne; Gieseke, Robert</p> <p>2017-04-01</p> <p>Pyhector is a Python interface for the simple climate model Hector (Hartin et al. 2015) developed in C++. Simple climate models like Hector can, for instance, be used in the analysis of scenarios within integrated assessment models like GCAM1, in the emulation of complex climate models, and in uncertainty analyses. Hector is an open-source, object oriented, simple global climate carbon cycle model. Its carbon cycle consists of a one pool atmosphere, three terrestrial pools which can be broken down into finer biomes or regions, and four carbon pools in the ocean component. The terrestrial carbon cycle includes primary production andmore » respiration fluxes. The ocean carbon cycle circulates carbon via a simplified thermohaline circulation, calculating air-sea fluxes as well as the marine carbonate system (Hartin et al. 2016). The model input is time series of greenhouse gas emissions; as example scenarios for these the Pyhector package contains the Representative Concentration Pathways (RCPs)2. These were developed to cover the range of baseline and mitigation emissions scenarios and are widely used in climate change research and model intercomparison projects. Using DataFrames from the Python library Pandas (McKinney 2010) as a data structure for the scenarios simplifies generating and adapting scenarios. Other parameters of the Hector model can easily be modified when running the model. Pyhector can be installed using pip from the Python Package Index.3 Source code and issue tracker are available in Pyhector's GitHub repository4. Documentation is provided through Readthedocs5. Usage examples are also contained in the repository as a Jupyter Notebook (Pérez and Granger 2007; Kluyver et al. 2016). Courtesy of the Mybinder project6, the example Notebook can also be executed and modified without installing Pyhector locally.« less</p> </li> <li> <p><a target="_blank" rel="noopener noreferrer" onclick="trackOutboundLink('http://adsabs.harvard.edu/abs/2017EGUGA..1915796W','NASAADS'); return false;" href="http://adsabs.harvard.edu/abs/2017EGUGA..1915796W"><span>Assessing global climate-terrestrial vegetation feedbacks on carbon and nitrogen cycling in the earth system model EC-Earth</span></a></p> <p><a target="_blank" rel="noopener noreferrer" href="http://adsabs.harvard.edu/abstract_service.html">NASA Astrophysics Data System (ADS)</a></p> <p>Wårlind, David; Miller, Paul; Nieradzik, Lars; Söderberg, Fredrik; Anthoni, Peter; Arneth, Almut; Smith, Ben</p> <p>2017-04-01</p> <p>There has been great progress in developing an improved European Consortium Earth System Model (EC-Earth) in preparation for the Coupled Model Intercomparison Project Phase 6 (CMIP6) and the next Assessment Report of the IPCC. The new model version has been complemented with ocean biogeochemistry, atmospheric composition (aerosols and chemistry) and dynamic land vegetation components, and has been configured to use the recommended CMIP6 forcing data sets. These new components will give us fresh insights into climate change. This study focuses on the terrestrial biosphere component Lund-Potsdam-Jena General Ecosystem Simulator (LPJ-GUESS) that simulates vegetation dynamics and compound exchange between the terrestrial biosphere and the atmosphere in EC-Earth. LPJ-GUESS allows for vegetation to dynamically evolve, depending on climate input, and in return provides the climate system and land surface scheme with vegetation-dependent fields such as vegetation types and leaf area index. We present the results of a study to examine the feedbacks between the dynamic terrestrial vegetation and the climate and their impact on the terrestrial ecosystem carbon and nitrogen cycles. Our results are based on a set of global, atmosphere-only historical simulations (1870 to 2014) with and without feedback between climate and vegetation and including or ignoring the effect of nitrogen limitation on plant productivity. These simulations show to what extent the addition degree of freedom in EC-Earth, introduced with the coupling of interactive dynamic vegetation to the atmosphere, has on terrestrial carbon and nitrogen cycling, and represent contributions to CMIP6 (C4MIP and LUMIP) and the EU Horizon 2020 project CRESCENDO.</p> </li> <li> <p><a target="_blank" rel="noopener noreferrer" onclick="trackOutboundLink('https://www.osti.gov/servlets/purl/1130968','SCIGOV-STC'); return false;" href="https://www.osti.gov/servlets/purl/1130968"><span>Novel Supercritical Carbon Dioxide Power Cycle Utilizing Pressured Oxy-combustion in Conjunction with Cryogenic Compression</span></a></p> <p><a target="_blank" rel="noopener noreferrer" href="http://www.osti.gov/search">DOE Office of Scientific and Technical Information (OSTI.GOV)</a></p> <p>Brun, Klaus; McClung, Aaron; Davis, John</p> <p>2014-03-31</p> <p>The team of Southwest Research Institute® (SwRI) and Thar Energy LLC (Thar) applied technology engineering and economic analysis to evaluate two advanced oxy-combustion power cycles, the Cryogenic Pressurized Oxy-combustion Cycle (CPOC), and the Supercritical Oxy-combustion Cycle. This assessment evaluated the performance and economic cost of the two proposed cycles with carbon capture, and included a technology gap analysis of the proposed technologies to determine the technology readiness level of the cycle and the cycle components. The results of the engineering and economic analysis and the technology gap analysis were used to identify the next steps along the technology development roadmapmore » for the selected cycle. The project objectives, as outlined in the FOA, were 90% CO{sub 2} removal at no more than a 35% increase in cost of electricity (COE) as compared to a Supercritical Pulverized Coal Plant without CO{sub 2} capture. The supercritical oxy-combustion power cycle with 99% carbon capture achieves a COE of $121/MWe. This revised COE represents a 21% reduction in cost as compared to supercritical steam with 90% carbon capture ($137/MWe). However, this represents a 49% increase in the COE over supercritical steam without carbon capture ($80.95/MWe), exceeding the 35% target. The supercritical oxy-combustion cycle with 99% carbon capture achieved a 37.9% HHV plant efficiency (39.3% LHV plant efficiency), when coupling a supercritical oxy-combustion thermal loop to an indirect supercritical CO{sub 2} (sCO{sub 2}) power block. In this configuration, the power block achieved 48% thermal efficiency for turbine inlet conditions of 650°C and 290 atm. Power block efficiencies near 60% are feasible with higher turbine inlet temperatures, however a design tradeoff to limit firing temperature to 650°C was made in order to use austenitic stainless steels for the high temperature pressure vessels and piping and to minimize the need for advanced turbomachinery features such as blade cooling. The overall technical readiness of the supercritical oxy-combustion cycle is TRL 2, Technology Concept, due to the maturity level of the supercritical oxy-combustor for solid fuels, and several critical supporting components, as identified in the Technical Gap Analysis. The supercritical oxycombustor for solid fuels operating at pressures near 100 atm is a unique component of the supercritical oxy-combustion cycle. In addition to the low TRL supercritical oxy-combustor, secondary systems were identified that would require adaptation for use with the supercritical oxycombustion cycle. These secondary systems include the high pressure pulverized coal feed, high temperature cyclone, removal of post-combustion particulates from the high pressure cyclone underflow stream, and micro-channel heat exchangers tolerant of particulate loading. Bench scale testing was utilized to measure coal combustion properties at elevated pressures in a CO{sub 2} environment. This testing included coal slurry preparation, visualization of coal injection into a high pressure fluid, and modification of existing test equipment to facilitate the combustion properties testing. Additional bench scale testing evaluated the effectiveness of a rotary atomizer for injecting a coal-water slurry into a fluid with similar densities, as opposed to the typical application where the high density fluid is injected into a low density fluid. The swirl type supercritical oxy-combustor was developed from initial concept to an advanced design stage through numerical simulation using FLUENT and Chemkin to model the flow through the combustor and provide initial assessment of the coal combustion reactions in the flow path. This effort enabled the initial combustor mechanical layout, initial pressure vessel design, and the conceptual layout of a pilot scale test loop. A pilot scale demonstration of the supercritical oxy-combustion cycle is proposed as the next step in the technology development. This demonstration would advance the supercritical oxy-combustion cycle and the supercritical oxy-combustor from a current TRL of 2, Technology Concept, to TRL 6, Pilot Scale System Demonstrated in a Relevant Environment, and enable the evaluation and continued refinement of the supercritical oxy-combustor and critical secondary systems.« less</p> </li> <li> <p><a target="_blank" rel="noopener noreferrer" onclick="trackOutboundLink('https://www.ncbi.nlm.nih.gov/pubmed/24804819','PUBMED'); return false;" href="https://www.ncbi.nlm.nih.gov/pubmed/24804819"><span>Origin and sources of dissolved organic matter in snow on the East Antarctic ice sheet.</span></a></p> <p><a target="_blank" rel="noopener noreferrer" href="https://www.ncbi.nlm.nih.gov/entrez/query.fcgi?DB=pubmed">PubMed</a></p> <p>Antony, Runa; Grannas, Amanda M; Willoughby, Amanda S; Sleighter, Rachel L; Thamban, Meloth; Hatcher, Patrick G</p> <p>2014-06-03</p> <p>Polar ice sheets hold a significant pool of the world's carbon reserve and are an integral component of the global carbon cycle. Yet, organic carbon composition and cycling in these systems is least understood. Here, we use ultrahigh resolution mass spectrometry to elucidate, at an unprecedented level, molecular details of dissolved organic matter (DOM) in Antarctic snow. Tens of thousands of distinct molecular species are identified, providing clues to the nature and sources of organic carbon in Antarctica. We show that many of the identified supraglacial organic matter formulas are consistent with material from microbial sources, and terrestrial inputs of vascular plant-derived materials are likely more important sources of organic carbon to Antarctica than previously thought. Black carbon-like material apparently originating from biomass burning in South America is also present, while a smaller fraction originated from soil humics and appears to be photochemically or microbially modified. In addition to remote continental sources, we document signals of oceanic emissions of primary aerosols and secondary organic aerosol precursors. The new insights on the diversity of organic species in Antarctic snowpack reinforce the importance of studying organic carbon associated with the Earth's polar regions in the face of changing climate.</p> </li> <li> <p><a target="_blank" rel="noopener noreferrer" onclick="trackOutboundLink('https://www.osti.gov/biblio/1342295-where-carbon-goes-when-water-flows-carbon-cycling-across-aquatic-continuum','SCIGOV-STC'); return false;" href="https://www.osti.gov/biblio/1342295-where-carbon-goes-when-water-flows-carbon-cycling-across-aquatic-continuum"><span>Where Carbon Goes When Water Flows: Carbon Cycling across the Aquatic Continuum</span></a></p> <p><a target="_blank" rel="noopener noreferrer" href="http://www.osti.gov/search">DOE Office of Scientific and Technical Information (OSTI.GOV)</a></p> <p>Ward, Nicholas D.; Bianchi, Thomas S.; Medeiros, Patricia M.</p> <p></p> <p>The purpose of this review is to highlight progress in unraveling carbon cycling dynamics across the continuum of landscapes, inland waters, coastal oceans, and the atmosphere. Earth systems are intimately interconnected, yet most biogeochemical studies focus on specific components in isolation. The movement of water drives the carbon cycle, and, as such, inland waters provide a critical intersection between terrestrial and marine biospheres. Inland, estuarine, and coastal waters are well studied in regions near centers of human population in the Northern hemisphere. However, many of the world’s large river systems and their marine receiving waters remain poorly characterized, particularly inmore » the tropics, which contribute to a disproportionately large fraction of the transformation of terrestrial organic matter to carbon dioxide, and the Arctic, where positive feedback mechanisms are likely to amplify global climate change. There are large gaps in current coverage of environmental observations along the aquatic continuum. For example, tidally-influenced reaches of major rivers and near-shore coastal regions around river plumes are often left out of carbon budgets due to a combination of methodological constraints and poor data coverage. We suggest that closing these gaps could potentially alter global estimates of CO2 outgassing from surface waters to the atmosphere by several-fold. Finally, in order to identify and constrain/embrace uncertainties in global carbon budget estimations it is important that we further adopt statistical and modeling approaches that have become well-established in the fields of oceanography and paleoclimatology, for example.« less</p> </li> <li> <p><a target="_blank" rel="noopener noreferrer" onclick="trackOutboundLink('https://pubs.er.usgs.gov/publication/70032956','USGSPUBS'); return false;" href="https://pubs.er.usgs.gov/publication/70032956"><span>Plumbing the global carbon cycle: Integrating inland waters into the terrestrial carbon budget</span></a></p> <p><a target="_blank" rel="noopener noreferrer" href="http://pubs.er.usgs.gov/pubs/index.jsp?view=adv">USGS Publications Warehouse</a></p> <p>Cole, J.J.; Prairie, Y.T.; Caraco, N.F.; McDowell, W.H.; Tranvik, L.J.; Striegl, Robert G.; Duarte, C.M.; Kortelainen, Pirkko; Downing, J.A.; Middelburg, J.J.; Melack, J.</p> <p>2007-01-01</p> <p>Because freshwater covers such a small fraction of the Earth's surface area, inland freshwater ecosystems (particularly lakes, rivers, and reservoirs) have rarely been considered as potentially important quantitative components of the carbon cycle at either global or regional scales. By taking published estimates of gas exchange, sediment accumulation, and carbon transport for a variety of aquatic systems, we have constructed a budget for the role of inland water ecosystems in the global carbon cycle. Our analysis conservatively estimates that inland waters annually receive, from a combination of background and anthropogenically altered sources, on the order of 1.9 Pg C y-1 from the terrestrial landscape, of which about 0.2 is buried in aquatic sediments, at least 0.8 (possibly much more) is returned to the atmosphere as gas exchange while the remaining 0.9 Pg y-1 is delivered to the oceans, roughly equally as inorganic and organic carbon. Thus, roughly twice as much C enters inland aquatic systems from land as is exported from land to the sea. Over prolonged time net carbon fluxes in aquatic systems tend to be greater per unit area than in much of the surrounding land. Although their area is small, these freshwater aquatic systems can affect regional C balances. Further, the inclusion of inland, freshwater ecosystems provides useful insight about the storage, oxidation and transport of terrestrial C, and may warrant a revision of how the modern net C sink on land is described. ?? 2007 Springer Science+Business Media, LLC.</p> </li> <li> <p><a target="_blank" rel="noopener noreferrer" onclick="trackOutboundLink('http://www.ars.usda.gov/research/publications/publication/?seqNo115=331937','TEKTRAN'); return false;" href="http://www.ars.usda.gov/research/publications/publication/?seqNo115=331937"><span>Multiscale analyses of solar-induced florescence and gross primary production</span></a></p> <p><a target="_blank" rel="noopener noreferrer" href="https://www.ars.usda.gov/research/publications/find-a-publication/">USDA-ARS?s Scientific Manuscript database</a></p> <p></p> <p></p> <p>Remotely sensed solar induced fluorescence (SIF) has shown great promise for probing spatiotemporal variations in terrestrial gross primary production (GPP), the largest component flux of the global carbon cycle. However, scale mismatches between SIF and ground-based GPP have posed challenges toward...</p> </li> <li> <p><a target="_blank" rel="noopener noreferrer" onclick="trackOutboundLink('http://adsabs.harvard.edu/abs/2017FrES...11..682Z','NASAADS'); return false;" href="http://adsabs.harvard.edu/abs/2017FrES...11..682Z"><span>Calcification response of Pleurochrysis carterae to iron concentrations in batch incubations: implication for the marine biogeochemical cycle</span></a></p> <p><a target="_blank" rel="noopener noreferrer" href="http://adsabs.harvard.edu/abstract_service.html">NASA Astrophysics Data System (ADS)</a></p> <p>Zou, Xiang; Sun, Shiyong; Lin, Sen; Shen, Kexuan; Dong, Faqin; Tan, Daoyong; Nie, Xiaoqin; Liu, Mingxue; Wei, Jie</p> <p>2017-12-01</p> <p>Calcified coccolithophores, a diverse and widely distributed group of marine microalgae, produce biogenic calcite in the form of coccoliths located on the cell surface. Using batch incubations of the coccolithophorid Pleurochrysis carterae, we investigated the responses of this calcification process to iron concentrations by changing the iron supply in the initial culture media from a normal concentration to 1 ppm (parts per million), 5 ppm, and 10 ppm. Time-dependent measurements of cell population, production of inorganic carbon (coccoliths), and organic carbon (organic cellular components) showed that elevated iron supply in the growth medium of P. carterae stimulates carbon sequestration by increasing growth along enhanced photosynthetic activity and calcification. In addition, the acquired time-dependent UV-Vis and FT-IR spectra revealed that iron fertilization-enhanced coccolith calcification is accompanied by a crystalline phase transition from calcite to aragonite or amorphous phase. Our results suggest that iron concentration has a significant influence on the marine carbon cycle of coccolithophores.</p> </li> <li> <p><a target="_blank" rel="noopener noreferrer" onclick="trackOutboundLink('http://adsabs.harvard.edu/abs/2017AGUFMPP13C1089T','NASAADS'); return false;" href="http://adsabs.harvard.edu/abs/2017AGUFMPP13C1089T"><span>Evaluating Carbon and Climate Sensitivities of the NOAA/GFDL Earth System Model ESM2Mb to Forcing Perturbations during the Paleocene-Eocene Thermal Maximum</span></a></p> <p><a target="_blank" rel="noopener noreferrer" href="http://adsabs.harvard.edu/abstract_service.html">NASA Astrophysics Data System (ADS)</a></p> <p>Tandy, H.; Shevliakova, E.; Keller, G.</p> <p>2017-12-01</p> <p>The Paleocene-Eocene Thermal Maximum (PETM, 55.5 Myr) was a period of rapid warming resulting from major changes in the carbon cycle and has been cited as the closest historical analogue to anthropogenic carbon release. Up to now, modeling studies of the PETM used either a low-resolution coupled model of the ocean and atmosphere with prescribed CO2 or CH4, or coupled climate-carbon models of intermediate complexity (i.e. simplified ocean or atmosphere). In this study we carried a suit of numerical experiments with the NOAA/GFDL comprehensive atmosphere-ocean coupled model with integrated terrestrial and marine carbon cycle components, known as an Earth System Model (ESM2Mb). We analyzed the output from millennia-scale ESM2Mb simulations with different combinations of forcings from the pre-PETM and PETM, including greenhouse gas concentrations and solar intensity. In addition we explore sensitivities of climate and carbon cycling to changes in geology such as topography, continental positions, and the presence and absence of large land glaciers. Furthermore, we examine ESM2Mb climate and carbon sensitivities to PETM conditions with a focus on how alternate conditions and forcings relate to the uncertainty in the climate and carbon cycling estimates from paleo observations. We explore changes in atmosphere, land, and ocean temperatures and circulation patterns as well as vegetation distribution, permafrost, and carbon storage in terrestrial and marine ecosystems from pre-PETM to PETM conditions. We found that with the present day land/sea mask and land glaciers in ESM2Mb, changes in only greenhouse gas concentrations (CO2 and CH4) from pre-PETM to PETM conditions induce global warming of 3-5 °C, consistent with the lower range of estimates from paleo proxies. Changes in the carbon permafrost storage from warming cannot explain the rapid increase in the atmospheric CO2 concentration. Changes in the ocean circulation and carbon storage critically depend on geological conditions such as continental positions. The study illustrates how models designed for studying future climate change can capture past paleo events, such as the PETM, and how modern day geological conditions may affect climate and carbon cycle sensitivities.</p> </li> <li> <p><a target="_blank" rel="noopener noreferrer" onclick="trackOutboundLink('https://www.osti.gov/biblio/1366373-investigation-autoclave-additive-manufacturing-composite-tooling','SCIGOV-STC'); return false;" href="https://www.osti.gov/biblio/1366373-investigation-autoclave-additive-manufacturing-composite-tooling"><span></span></a></p> <p><a target="_blank" rel="noopener noreferrer" href="http://www.osti.gov/search">DOE Office of Scientific and Technical Information (OSTI.GOV)</a></p> <p>Kunc, Vlastimil; Lindahl, John M; Dinwiddie, Ralph Barton</p> <p></p> <p>The autoclave is a crucial piece of equipment for fabricating Tier 1 polymer composite aerospace structural components with very low void content (i.e. < 5 %). The essential component in this composite manufacturing process is the rigid mold that defines the final shape of the fabricated composite component. The Big Area Additive Manufacturing (BAAM) system located at Oak Ridge National Laboratory s (ORNL) Manufacturing Demonstration Facility (MDF) has been used to manufacture a new generation of in-autoclave tools that can be used to fabricate various aerospace composite parts. Different tools made form Polyphenylene sulfide (PPS) with 50 % by weightmore » carbon fiber and Polyphenylsulfone (PPSU) with 25 % carbon fiber are investigated in this study. The behavior of the printed tools under different temperature ramp rates for the autoclave cycles was observed and analyzed.« less</p> </li> <li> <p><a target="_blank" rel="noopener noreferrer" onclick="trackOutboundLink('http://adsabs.harvard.edu/abs/2017AGUFM.B41B1942B','NASAADS'); return false;" href="http://adsabs.harvard.edu/abs/2017AGUFM.B41B1942B"><span>Molecular Analysis of Flood Deposits in the Tennessee River Valley: Implications for Understanding Carbon Cycling in Fluvial Environments and Anthropogenic Impacts</span></a></p> <p><a target="_blank" rel="noopener noreferrer" href="http://adsabs.harvard.edu/abstract_service.html">NASA Astrophysics Data System (ADS)</a></p> <p>Blackaby, E.; Craven, O. D.; Hockaday, W. C.; Forman, S. L.; Stinchcomb, G. E.</p> <p>2017-12-01</p> <p>The middle Tennessee River Valley contains both historic and prehistoric (>AD 1600) flood deposits. Stratigraphic sequences of stacked flood deposits that often bury soils provide new insights on organic matter transported and preserved prior to and after European colonization. This study focused on understanding carbon cycling within a dynamic fluvial system and quantifying the anthropogenic effect on flood processes through the analysis of molecular components of the organic matter. The data may be helpful in discerning the organic geochemical fingerprint for historic and prehistoric flood deposits. Ten samples were collected from three sites at varying depths and dated using optically stimulated luminescence (OSL). All samples underwent solid-state cross polar 13C NMR analysis at twelve kilohertz, and a molecular mixing model (MMM) was used to determine the molecular components of the organic matter present in each sample. The MMM categorized carbon molecules present in each sample in terms of carbohydrate, protein, lipid, lignin, char, or pure carbonyl. Char was the most prominent molecular component of all ten samples ranging from 28.7 to 55.9% and comprised larger percentages in prehistoric deposits. The historic deposits, while still char dominated, showed more molecular diversity with higher percentages in non-char carbon groups. The carbonyl, lipid, and carbohydrate groups are present throughout all the samples with the carbonyl ranging from 9.3 to 31.4%, the lipid from 5.5 to 16.7%, and the carbohydrate from 4.4 to 16.9%. The high amount of carbonyl throughout the samples indicates that the deposits existed in a highly oxidizing environment. Differences in the presence and amount of carbon groups between historic and prehistoric flood deposits potentially reflect diagenic alternation of organic matter through time, changes in human land use, or some combination processes. These preliminary results possibly indicate changes in carbon pools accessed with European cultivation and continued degradation of organic moieties during a ca. 400 years burial, and mostly in oxidizing conditions.</p> </li> <li> <p><a target="_blank" rel="noopener noreferrer" onclick="trackOutboundLink('https://www.ncbi.nlm.nih.gov/pubmed/26070189','PUBMED'); return false;" href="https://www.ncbi.nlm.nih.gov/pubmed/26070189"><span>Manganese oxide nanowires wrapped with nitrogen doped carbon layers for high performance supercapacitors.</span></a></p> <p><a target="_blank" rel="noopener noreferrer" href="https://www.ncbi.nlm.nih.gov/entrez/query.fcgi?DB=pubmed">PubMed</a></p> <p>Li, Ying; Mei, Yuan; Zhang, Lin-Qun; Wang, Jian-Hai; Liu, An-Ran; Zhang, Yuan-Jian; Liu, Song-Qin</p> <p>2015-10-01</p> <p>In this study, manganese oxide nanowires wrapped by nitrogen-doped carbon layers (MnO(x)@NCs) were prepared by carbonization of poly(o-phenylenediamine) layer coated onto MnO2 nanowires for high performance supercapacitors. The component and structure of the MnO(x)@NCs were controlled through carbonization procedure under different temperatures. Results demonstrated that this composite combined the high conductivity and high specific surface area of nitrogen-doped carbon layers with the high pseudo-capacitance of manganese oxide nanowires. The as-prepared MnO(x)@NCs exhibited superior capacitive properties in 1 M Na2SO4 aqueous solution, such as high conductivity (4.167×10(-3) S cm(-1)), high specific capacitance (269 F g(-1) at 10 mV s(-1)) and long cycle life (134 F g(-1) after 1200 cycles at a scan rate of 50 mV s(-1)). It is reckoned that the present novel hybrid nanowires can serve as a promising electrode material for supercapacitors and other electrochemical devices. Copyright © 2015 Elsevier Inc. All rights reserved.</p> </li> <li> <p><a target="_blank" rel="noopener noreferrer" onclick="trackOutboundLink('http://adsabs.harvard.edu/abs/2011AGUFMPP32A..05W','NASAADS'); return false;" href="http://adsabs.harvard.edu/abs/2011AGUFMPP32A..05W"><span>Influence of Large Lakes on Methane Greenhouse Forcing in the Early Eocene</span></a></p> <p><a target="_blank" rel="noopener noreferrer" href="http://adsabs.harvard.edu/abstract_service.html">NASA Astrophysics Data System (ADS)</a></p> <p>Whiteside, J. H.; Granberg, D. L.; Kasprak, A. H.; Taylor, K. W.; Pancost, R. D.</p> <p>2011-12-01</p> <p>Long-duration elevated global temperatures and increased atmospheric pCO2 levels (~1000-2000 ppm) characterized the earliest portion of the Eocene (Ypressian; ~55 to 49 Ma). This extended period of global warmth was also punctuated by a series of short (sub-precessional) hyperthermal events in which atmospheric CO2 (>2000 ppm) and global temperatures rose with unprecedented and (as of yet) unexplained rapidity. This interval is perhaps the best temporal analog for assessing contemporary response of the biosphere and global carbon cycle to increased CO2 emissions. Although these hyperthermals appear paced by 100 Ka and 1 Ma scale orbital (eccentricity) cycles in the marine realm, high frequency forcing processes have not yet been examined, and long continental records have yet to be explored for their expression. To identify sub-eccentricity (<100,000 year) scale variability in Early Eocene carbon cycling, we examined lacustrine records of organic carbon isotopes and carbon content from a ~5 Ma record in the Green River Formation (GRF) in the Uinta Basin of Utah, U.S.A. and a ~1 Ma record from the Messel Shale, (Darmstadt, Germany.) We demonstrate that in addition to the expected 100 Ka eccentricity cycle, the 40 Ka cycle of obliquity is also an important component of climate variability as reflected in the lacustrine carbon cycle and hence a potential driver of global carbon cycling. We further investigated carbon cycle dynamics by examining biomarker evidence for changes in the terrestrial methane cycle during this time interval. Due to their increased volumes (>60,000 km2), highly stratified and cyclically anoxic lakes of the Eocene could have provided enough methane to alter global radiative forcing. This is consistent with our data, which demonstrate that the GRF and Messel Shale both exhibit strongly reducing conditions as well as abundant methanogen and methanotroph biomarkers. Further, the GRF lacustrine environment was highly stratified with, at times, euxinic waters extending into the photic zone, as inferred from the presence of isorenieratene derivatives. Thus, the GRF was likely an area of elevated methanogenic activity during this time. Increasing input of terrestrial matter into the GRF correlates with shifts in the pristane/phytane ratio and isorenieratane abundances, suggesting that increased runoff intensified the stratification of the lake with a transition to more anoxic conditions. Following this transition, it is likely that methane production in the GRF lake increased, which released more into the atmosphere. Our new results suggest that the global carbon cycle of the early Eocene greenhouse world was strongly mediated by both astronomical forcing (including obliquity) and increased methane production in large stratified lakes.</p> </li> <li> <p><a target="_blank" rel="noopener noreferrer" onclick="trackOutboundLink('http://adsabs.harvard.edu/abs/2013AGUFMOS13C1712H','NASAADS'); return false;" href="http://adsabs.harvard.edu/abs/2013AGUFMOS13C1712H"><span>Palaeo-equatorial temperatures and carbon-cycle evolution at the Triassic- Jurassic boundary: A stable isotope perspective from shallow-water carbonates from the UAE</span></a></p> <p><a target="_blank" rel="noopener noreferrer" href="http://adsabs.harvard.edu/abstract_service.html">NASA Astrophysics Data System (ADS)</a></p> <p>Honig, M. R.; John, C. M.</p> <p>2013-12-01</p> <p>The Triassic-Jurassic boundary was marked by global changes including carbon-cycle perturbations and the opening of the Atlantic Ocean. These changes were accompanied by one of the major extinction events of the Phanerozoic. The carbon-cycle perturbations have been recorded in carbon isotope curves from bulk carbonates, organic carbon and fossil wood in several Tethyan locations and have been used for chemostratigraphic purposes. Here we present data from shallow-marine carbonates deposited on a homoclinal Middle Eastern carbonate ramp (United Arab Emirates). Our site was located at the equator throughout the Late Triassic and the Early Jurassic, and this study provides the first constraints of environmental changes at the low-latitudes for the Triassic-Jurassic boundary. Shallow-marine carbonate depositional systems are extremely sensitive to palaeoenvironmental changes and their usefulness for chemostratigraphy is being debated. However, the palaeogeographic location of the studied carbonate ramp gives us a unique insight into a tropical carbonate factory at a time of severe global change. Stable isotope measurements (carbon and oxygen) are being carried out on micrite, ooids and shell material along the Triassic-Jurassic boundary. The stable isotope results on micrite show a prominent negative shift in carbon isotope values of approximately 2 ‰ just below the inferred position of the Triassic-Jurassic boundary. A similar isotopic trend is also observed across the Tethys but with a range of amplitudes (from ~2 ‰ to ~4 ‰). These results seem to indicate that the neritic carbonates from our studied section can be used for chemostratigraphic purposes, and the amplitudes of the carbon isotope shifts provide critical constraints on the magnitude of carbon-cycle perturbations at low latitudes across the Triassic-Jurassic boundary. Seawater temperatures across the Triassic-Jurassic boundary will be constrained using the clumped isotope palaeo-thermometer applied to blocky calcite, bulk carbonate, oyster shells and echinoids. Assuming a pristine depositional signal can be extracted from one of the components, clumped isotopes will either shed light on the palaeoenvironmental conditions and the isotopic composition of a tropical ocean during the Late Triassic / Early Jurassic, or on the diagenetic history of the platform. We gratefully acknowledge funding from Qatar Petroleum, Shell, and Qatar Science & Technology Park.</p> </li> </ol> <div class="pull-right"> <ul class="pagination"> <li><a href="#" onclick='return showDiv("page_1");'>«</a></li> <li><a href="#" onclick='return showDiv("page_6");'>6</a></li> <li><a href="#" onclick='return showDiv("page_7");'>7</a></li> <li class="active"><span>8</span></li> <li><a href="#" onclick='return showDiv("page_9");'>9</a></li> <li><a href="#" onclick='return showDiv("page_10");'>10</a></li> <li><a href="#" onclick='return showDiv("page_25");'>»</a></li> </ul> </div> </div><!-- col-sm-12 --> </div><!-- row --> </div><!-- page_8 --> <div id="page_9" class="hiddenDiv"> <div class="row"> <div class="col-sm-12"> <div class="pull-right"> <ul class="pagination"> <li><a href="#" onclick='return showDiv("page_1");'>«</a></li> <li><a href="#" onclick='return showDiv("page_7");'>7</a></li> <li><a href="#" onclick='return showDiv("page_8");'>8</a></li> <li class="active"><span>9</span></li> <li><a href="#" onclick='return showDiv("page_10");'>10</a></li> <li><a href="#" onclick='return showDiv("page_11");'>11</a></li> <li><a href="#" onclick='return showDiv("page_25");'>»</a></li> </ul> </div> </div> </div> <div class="row"> <div class="col-sm-12"> <ol class="result-class" start="161"> <li> <p><a target="_blank" rel="noopener noreferrer" onclick="trackOutboundLink('http://adsabs.harvard.edu/abs/2015ECSS..159...37Y','NASAADS'); return false;" href="http://adsabs.harvard.edu/abs/2015ECSS..159...37Y"><span>Dynamics of dissolved organic matter in fjord ecosystems: Contributions of terrestrial dissolved organic matter in the deep layer</span></a></p> <p><a target="_blank" rel="noopener noreferrer" href="http://adsabs.harvard.edu/abstract_service.html">NASA Astrophysics Data System (ADS)</a></p> <p>Yamashita, Youhei; McCallister, S. Leigh; Koch, Boris P.; Gonsior, Michael; Jaffé, Rudolf</p> <p>2015-06-01</p> <p>Annually, rivers and inland water systems deliver a significant amount of terrestrial organic matter (OM) to the adjacent coastal ocean in both particulate and dissolved forms; however, the metabolic and biogeochemical transformations of OM during its seaward transport remains one of the least understood components of the global carbon cycle. This transfer of terrestrial carbon to marine ecosystems is crucial in maintaining trophic dynamics in coastal areas and critical in global carbon cycling. Although coastal regions have been proposed as important sinks for exported terrestrial materials, most of the global carbon cycling data, have not included fjords in their budgets. Here we present distributional patterns on the quantity and quality of dissolved OM in Fiordland National Park, New Zealand. Specifically, we describe carbon dynamics under diverse environmental settings based on dissolved organic carbon (DOC) depth profiles, oxygen concentrations, optical properties (fluorescence) and stable carbon isotopes. We illustrate a distinct change in the character of DOC in deep waters compared to surface and mid-depth waters. Our results suggest that, both, microbial reworking of terrestrially derived plant detritus and subsequent desorption of DOC from its particulate counterpart (as verified in a desorption experiment) are the main sources of the humic-like enriched DOC in the deep basins of the studied fjords. While it has been suggested that short transit times and protection of OM by mineral sorption may ultimately result in significant terrestrial carbon burial and preservation in fjords, our data suggests the existence of an additional source of terrestrial OM in the form of DOC generated in deep, fjord water.</p> </li> <li> <p><a target="_blank" rel="noopener noreferrer" onclick="trackOutboundLink('https://www.ncbi.nlm.nih.gov/pubmed/18491697','PUBMED'); return false;" href="https://www.ncbi.nlm.nih.gov/pubmed/18491697"><span>Tribological assessment of a flexible carbon-fibre-reinforced poly(ether-ether-ketone) acetabular cup articulating against an alumina femoral head.</span></a></p> <p><a target="_blank" rel="noopener noreferrer" href="https://www.ncbi.nlm.nih.gov/entrez/query.fcgi?DB=pubmed">PubMed</a></p> <p>Scholes, S C; Inman, I A; Unsworth, A; Jones, E</p> <p>2008-04-01</p> <p>New material combinations have been introduced as the bearing surfaces of hip prostheses in an attempt to prolong their life by overcoming the problems of failure due to wear-particle-induced osteolysis. This will hopefully reduce the need for revision surgery. The study detailed here used a hip simulator to assess the volumetric wear rates of large-diameter carbon-fibre-reinforced pitch-based poly(ether-ether-ketone) (CFR-PEEK) acetabular cups articulating against alumina femoral heads. The joints were tested for 25 x 10(6) cycles. Friction tests were also performed on these joints to determine the lubrication regime under which they operate. The average volumetric wear rate of the CFR-PEEK acetabular component of 54 mm diameter was 1.16 mm(3)/10(6) cycles, compared with 38.6 mm(3)/10(6) cycles for an ultra-high-molecular-weight polyethylene acetabular component of 28 mm diameter worn against a ceramic head. This extremely low wear rate was sustained over 25 x 10(6) cycles (the equivalent of up to approximately 25 years in vivo). The frictional studies showed that the joints worked under the mixed-boundary lubrication regime. The low wear produced by these joints showed that this novel joint couple offers low wear rates and therefore may be an alternative material choice for the reduction of osteolysis.</p> </li> <li> <p><a target="_blank" rel="noopener noreferrer" onclick="trackOutboundLink('https://www.ncbi.nlm.nih.gov/pubmed/26501378','PUBMED'); return false;" href="https://www.ncbi.nlm.nih.gov/pubmed/26501378"><span>A significant carbon sink in temperate forests in Beijing: based on 20-year field measurements in three stands.</span></a></p> <p><a target="_blank" rel="noopener noreferrer" href="https://www.ncbi.nlm.nih.gov/entrez/query.fcgi?DB=pubmed">PubMed</a></p> <p>Zhu, JianXiao; Hu, XueYang; Yao, Hui; Liu, GuoHua; Ji, ChenJun; Fang, JingYun</p> <p>2015-11-01</p> <p>Numerous efforts have been made to characterize forest carbon (C) cycles and stocks in various ecosystems. However, long-term observation on each component of the forest C cycle is still lacking. We measured C stocks and fluxes in three permanent temperate forest plots (birch, oak and pine forest) during 2011–2014, and calculated the changes of the components of the C cycle related to the measurements during 1992–1994 at Mt. Dongling, Beijing, China. Forest net primary production in birch, oak, and pine plots was 5.32, 4.53, and 6.73 Mg C ha-1 a-1, respectively. Corresponding net ecosystem production was 0.12, 0.43, and 3.53 Mg C ha-1 a-1. The C stocks and fluxes in 2011–2014 were significantly larger than those in 1992–1994 in which the biomass C densities in birch, oak, and pine plots increased from 50.0, 37.7, and 54.0 Mg C ha-1 in 1994 to 101.5, 77.3, and 110.9 Mg C ha-1 in 2014; soil organic C densities increased from 207.0, 239.1, and 231.7 Mg C ha-1 to 214.8, 241.7, and 238.4 Mg C ha-1; and soil heterotrophic respiration increased from 2.78, 3.49, and 1.81 Mg C ha-1 a-1 to 5.20, 4.10, and 3.20 Mg C ha-1 a-1. These results suggest that the mountainous temperate forest ecosystems in Beijing have served as a carbon sink in the last two decades. These observations of C stocks and fluxes provided field-based data for a long-term study of C cycling in temperate forest ecosystems.</p> </li> <li> <p><a target="_blank" rel="noopener noreferrer" onclick="trackOutboundLink('http://adsabs.harvard.edu/abs/2016AGUOSAH34A0063D','NASAADS'); return false;" href="http://adsabs.harvard.edu/abs/2016AGUOSAH34A0063D"><span>Impacts of the Nutrient Inputs from Riverine on the Dynamic and Community Structure of Fungal-like Protists in the Coastal Ocean Ecosystems</span></a></p> <p><a target="_blank" rel="noopener noreferrer" href="http://adsabs.harvard.edu/abstract_service.html">NASA Astrophysics Data System (ADS)</a></p> <p>Duan, Y.; Wang, G.; Xie, N.</p> <p>2016-02-01</p> <p>The coastal ocean connects terrestrial (e.g., rivers and estuaries) with oceanic ecosystems and is considered as a major component of global carbon cycles and budgets. The coastal waters are featured with a high biodiversity and high primary production. Because of the excessive primary production, a large fraction of primary organic matter becomes available to consumers as detritus in the coastal waters. Bacterioplankton have long been known to play a key role in the degradation of this detritus, and export and storage of organic matter in the coastal ecosystems. However, the primary and secondary production and the carbon biogeochemical processes in the ecosystems are largely regulated by nutrient inputs from riverine and other anthropogenic activities through heterotrophic microbial communities. Thraustochytrids, commonly known as fungal-like protists, are unicellular heterotrophic protists and are recently acknowledged to play a significant role in ocean carbon cycling. Their abundance exceeds that of bacterioplankton in the most time of the year in the coastal waters of China. Also, their abundance and diversity are largely regulated by nutrients inputs from riverine and other anthropogenic activities. Our findings support that thraustochytrids are a dominant heterotrophic microbial group in the coastal waters. Evidently, thraustochytrids are an import, but neglected, component in microbial carbon biogeochemical processes of the coastal ocean.</p> </li> <li> <p><a target="_blank" rel="noopener noreferrer" onclick="trackOutboundLink('http://adsabs.harvard.edu/abs/2017JPS...365...68P','NASAADS'); return false;" href="http://adsabs.harvard.edu/abs/2017JPS...365...68P"><span>Enhanced electrochemical performance of Li-rich layered cathode materials via chemical activation of Li2MnO3 component and formation of spinel/carbon coating layer</span></a></p> <p><a target="_blank" rel="noopener noreferrer" href="http://adsabs.harvard.edu/abstract_service.html">NASA Astrophysics Data System (ADS)</a></p> <p>Pang, Shengli; Xu, Kaijie; Wang, Yonggang; Shen, Xiangqian; Wang, Wenzhi; Su, Yanjing; Zhu, Meng; Xi, Xiaoming</p> <p>2017-10-01</p> <p>Li-rich layered oxides are promising cathode materials for advanced Li-ion batteries because of their high specific capacity and operating potential. In this work, the Li-rich layered oxide Li1·2Mn0·54Ni0·13Co0·13O2 (LMNC), is modified via a carbonization-reduction process (yielding the corresponding reduced compound denoted LMNC-R). Compared to the pristine oxide, LMNC-R delivers significantly enhanced initial discharge capacity/columbic efficiency, remarkably improved rate performance with an accelerated Li+ diffusion rate, and significantly increased capacity/voltage retention. The specific energy density and energy retention after 100 cycles increase from 378.2 Wh kg-1 and 47.7% for LMNC to 572.0 Wh kg-1 and 71.3%, respectively, for LMNC-R. The enhancement in the electrochemical performance of LMNC-R can be attributed to the synchronous formation of the oxygen non-stoichiometric Li2MnO3-δ component and to the carbon/spinel double coating layer in the material that resulted from the post-treatment process. Thus, the carbonization-reduction modification process can be used to tailor the structural evolution procedure and to suppress the metal ion dissolution of the Li-rich layered oxide during cycling.</p> </li> <li> <p><a target="_blank" rel="noopener noreferrer" onclick="trackOutboundLink('http://adsabs.harvard.edu/abs/2017APS..MARS36012W','NASAADS'); return false;" href="http://adsabs.harvard.edu/abs/2017APS..MARS36012W"><span>Adsorption of Natural Gas Mixtures in Nanoporos Carbon</span></a></p> <p><a target="_blank" rel="noopener noreferrer" href="http://adsabs.harvard.edu/abstract_service.html">NASA Astrophysics Data System (ADS)</a></p> <p>Wexler, Carlos; Crawford-Goss, Ian; Lemke, Drew; Roth, Michael</p> <p></p> <p>Natural gas (NG) is promising fuel due to its smaller CO2 emissions per unit energy compared to other hydrocarbons. Storage via adsorption into carbon nanostructures permits the operation of storage tanks at significantly reduced pressures, resulting in cost savings, added safety and smaller loss of cargo volume. Since NG is mostly comprised of methane (87-99%), other components are often ignored, even though heavier species are likely to adsorb preferentially and possibly result in long-term performance issues. We performed Molecular Dynamics (MD) simulations to understand the behavior of heavier components of NG adsorbed into carbon nanostructures. We focused on mixtures involving methane, ethane and propane. We show that the heavier components have significant preferential adsorption, partially inhibiting the adsorption of methane, and resulting in its saturation at lower pressures. Under room temperature conditions, propane adsorbs quasi irrevesibly, though remaining mobile within the pores. We discuss the diffusion regime of all gases and address methods to remove the adsorbed heavier gases by thermal cycling the tank. American Chemical Society Petroleum Research Fund.</p> </li> <li> <p><a target="_blank" rel="noopener noreferrer" onclick="trackOutboundLink('https://www.ncbi.nlm.nih.gov/pubmed/24526588','PUBMED'); return false;" href="https://www.ncbi.nlm.nih.gov/pubmed/24526588"><span>Dynamic energy budget modeling reveals the potential of future growth and calcification for the coccolithophore Emiliania huxleyi in an acidified ocean.</span></a></p> <p><a target="_blank" rel="noopener noreferrer" href="https://www.ncbi.nlm.nih.gov/entrez/query.fcgi?DB=pubmed">PubMed</a></p> <p>Muller, Erik B; Nisbet, Roger M</p> <p>2014-06-01</p> <p>Ocean acidification is likely to impact the calcification potential of marine organisms. In part due to the covarying nature of the ocean carbonate system components, including pH and CO2 and CO3(2-) levels, it remains largely unclear how each of these components may affect calcification rates quantitatively. We develop a process-based bioenergetic model that explains how several components of the ocean carbonate system collectively affect growth and calcification rates in Emiliania huxleyi, which plays a major role in marine primary production and biogeochemical carbon cycling. The model predicts that under the IPCC A2 emission scenario, its growth and calcification potential will have decreased by the end of the century, although those reductions are relatively modest. We anticipate that our model will be relevant for many other marine calcifying organisms, and that it can be used to improve our understanding of the impact of climate change on marine systems. © 2014 John Wiley & Sons Ltd.</p> </li> <li> <p><a target="_blank" rel="noopener noreferrer" onclick="trackOutboundLink('https://www.osti.gov/servlets/purl/943554','SCIGOV-STC'); return false;" href="https://www.osti.gov/servlets/purl/943554"><span>Cycling of DOC and DON by Novel Heterotrophic and Photoheterotrophic Bacteria in the Ocean: Final Report</span></a></p> <p><a target="_blank" rel="noopener noreferrer" href="http://www.osti.gov/search">DOE Office of Scientific and Technical Information (OSTI.GOV)</a></p> <p>Kirchman, David L.</p> <p>2008-12-09</p> <p>The flux of dissolved organic matter (DOM) through aquatic bacterial communities is a major process in carbon cycling in the oceans and other aquatic systems. Our work addressed the general hypothesis that the phylogenetic make-up of bacterial communities and the abundances of key types of bacteria are important factors influencing the processing of DOM in aquatic ecosystems. Since most bacteria are not easily cultivated, the phylogenetic diversity of these microbes has to be assessed using culture-independent approaches. Even if the relevant bacteria were cultivated, their activity in the lab would likely differ from that under environmental conditions. This project foundmore » variation in DOM uptake by the major bacterial groups found in coastal waters. In brief, the data suggest substantial differences among groups in the use of high and molecular weight DOM components. It also made key discoveries about the role of light in affecting this uptake especially by cyanobacteria. In the North Atlantic Ocean, for example, over half of the light-stimulated uptake was by the coccoid cyanobacterium, Prochlorococcus, with the remaining uptake due to Synechococcus and other photoheterotrophic bacteria. The project also examined in detail the degradation of one organic matter component, chitin, which is often said to be the second most abundant compound in the biosphere. The findings of this project contribute to our understanding of DOM fluxes and microbial dynamics supported by those fluxes. It is possible that these findings will lead to improvements in models of the carbon cycle that have compartments for dissolved organic carbon (DOC), the largest pool of organic carbon in the oceans.« less</p> </li> <li> <p><a target="_blank" rel="noopener noreferrer" onclick="trackOutboundLink('http://adsabs.harvard.edu/abs/2009ERL.....4c4011S','NASAADS'); return false;" href="http://adsabs.harvard.edu/abs/2009ERL.....4c4011S"><span>Global warming potential of pavements</span></a></p> <p><a target="_blank" rel="noopener noreferrer" href="http://adsabs.harvard.edu/abstract_service.html">NASA Astrophysics Data System (ADS)</a></p> <p>Santero, Nicholas J.; Horvath, Arpad</p> <p>2009-09-01</p> <p>Pavements comprise an essential and vast infrastructure system supporting our transportation network, yet their impact on the environment is largely unquantified. Previous life-cycle assessments have only included a limited number of the applicable life-cycle components in their analysis. This research expands the current view to include eight different components: materials extraction and production, transportation, onsite equipment, traffic delay, carbonation, lighting, albedo, and rolling resistance. Using global warming potential as the environmental indicator, ranges of potential impact for each component are calculated and compared based on the information uncovered in the existing research. The relative impacts between components are found to be orders of magnitude different in some cases. Context-related factors, such as traffic level and location, are also important elements affecting the impacts of a given component. A strategic method for lowering the global warming potential of a pavement is developed based on the concept that environmental performance is improved most effectively by focusing on components with high impact potentials. This system takes advantage of the fact that small changes in high-impact components will have more effect than large changes in low-impact components.</p> </li> <li> <p><a target="_blank" rel="noopener noreferrer" onclick="trackOutboundLink('http://adsabs.harvard.edu/abs/2003EAEJA.....4984B','NASAADS'); return false;" href="http://adsabs.harvard.edu/abs/2003EAEJA.....4984B"><span>Towards a community Earth System Model</span></a></p> <p><a target="_blank" rel="noopener noreferrer" href="http://adsabs.harvard.edu/abstract_service.html">NASA Astrophysics Data System (ADS)</a></p> <p>Blackmon, M.</p> <p>2003-04-01</p> <p>The Community Climate System Model, version 2 (CCSM2), was released in June 2002. CCSM2 has several new components and features, which I will discuss briefly. I will also show a few results from a multi-century equilibrium run with this model, emphasizing the improvements over the earlier simulation using the original CSM. A few flaws and inadequacies in CCSM2 have been identified. I will also discuss briefly work underway to improve the model and present results, if available. CCSM2, with improvements, will be the basis for the development of a Community Earth System Model (CESM). The highest priority for expansion of the model involves incorporation of biogeosciences into the coupled model system, with emphasis given to the carbon, nitrogen and iron cycles. The overall goal of the biogeosciences project within CESM is to understand the regulation of planetary energetics, planetary ecology, and planetary metabolism through exchanges of energy, momentum, and materials among atmosphere, land, and ocean, and the response of the climate system through these processes to changes in land cover and land use. In particular, this research addresses how biogeochemical coupling of carbon, nitrogen, and iron cycles affects climate and how human perturbations of these cycles alter climate. To accomplish these goals, the Community Land Model, the land component of CCSM2, is being developed to include river routing, carbon and nitrogen cycles, emissions of mineral aerosols and biogenic volatile organic compounds, dry deposition of various gases, and vegetation dynamics. The carbon and nitrogen cycles are being implemented using parameterizations developed as part of a state-of-the-art ecosystem biogeochemistry model. The primary goal of this research is to provide an accurate net flux of CO2 between the land and the atmosphere so that CESM can be used to study the dynamics of the coupled climate-carbon system. Emissions of biogenic volatile organic compounds are also based on a state-of-the-art emissions model and depend on plant type, leaf area index, photosynthetically active radiation, and leaf temperature. Dust emissions and deposition are being developed to implement a fully coupled dust cycle in CCSM, including the radiative effects of dust and carbon feedbacks related to fertilization of ocean and terrestrial ecosystems. Dust mobilization depends on surface wind speed, soil moisture, plant cover, and soil texture. Dust dry deposition processes include sedimentation and turbulent mix-out. A major research focus is how natural and human-mediated changes in land cover and ecosystem functions alter surface energy fluxes, the hydrological cycle, and biogeochemical cycles. Human land uses include conversion of natural vegetation to cropland, soil degradation, and urbanization. Climate feedbacks associated with natural changes in land cover are being assessed by developing and implementing a model of natural vegetation dynamics for use with the Community Land Model. Development of a marine ecosystem model is also underway. The ecosystem model is based on the global, mixed-layer marine ecosystem model of Moore et al., which includes parameterizations for such things as iron limitation and scavenging, zooplankton grazing, nitrogen fixation, calcification, and ballast-based remineralization. A series of experiments is being planned to assess the coupling of the ecology to the biogeochemistry, to adequately tune some of the model parameters that are poorly constrained by data, to explore new parameterizations and processes (e.g., riverine and atmospheric inputs of nutrients), and to conduct uncoupled application studies (e.g., deliberate carbon sequestration, retrospective historical simulations, iron-dust deposition response). Longer term plans include investigating biogeochemical processes in the coastal zone and how to incorporate these processes into a global ocean model, either through subgrid-scale parameterizations or model nesting. A Whole Atmosphere Community Climate Model(WACCM) is being developed. The vertical extent of the model is 150 km at present, but extension to 500 km is eventually expected. Interactive chemistry is being incorporated. This model will be used as the atmospheric component of CESM for some experiments. One expected application is the study of solar variability and its impact on climate variability in the troposphere and at the atmosphere, ocean, land interface. Preliminary results using some of these model components will be shown. A timeline for development and use of the models will be given.</p> </li> <li> <p><a target="_blank" rel="noopener noreferrer" onclick="trackOutboundLink('https://www.ncbi.nlm.nih.gov/pubmed/25071186','PUBMED'); return false;" href="https://www.ncbi.nlm.nih.gov/pubmed/25071186"><span>Sphalerite is a geochemical catalyst for carbon-hydrogen bond activation.</span></a></p> <p><a target="_blank" rel="noopener noreferrer" href="https://www.ncbi.nlm.nih.gov/entrez/query.fcgi?DB=pubmed">PubMed</a></p> <p>Shipp, Jessie A; Gould, Ian R; Shock, Everett L; Williams, Lynda B; Hartnett, Hilairy E</p> <p>2014-08-12</p> <p>Reactions among minerals and organic compounds in hydrothermal systems are critical components of the Earth's deep carbon cycle, provide energy for the deep biosphere, and may have implications for the origins of life. However, there is limited information as to how specific minerals influence the reactivity of organic compounds. Here we demonstrate mineral catalysis of the most fundamental component of an organic reaction: the breaking and making of a covalent bond. In the absence of mineral, hydrothermal reaction of cis- and trans-1,2-dimethylcyclohexane is extremely slow and generates many products. In the presence of sphalerite (ZnS), however, the reaction rate increases dramatically and one major product is formed: the corresponding stereoisomer. Isotope studies show that the sphalerite acts as a highly specific heterogeneous catalyst for activation of a single carbon-hydrogen bond in the dimethylcyclohexanes.</p> </li> <li> <p><a target="_blank" rel="noopener noreferrer" onclick="trackOutboundLink('https://www.osti.gov/pages/biblio/1198058-variable-stoichiometry-dissolved-organic-matter-cycling-community-earth-system-model','SCIGOV-DOEP'); return false;" href="https://www.osti.gov/pages/biblio/1198058-variable-stoichiometry-dissolved-organic-matter-cycling-community-earth-system-model"><span>Variable C : N : P stoichiometry of dissolved organic matter cycling in the Community Earth System Model</span></a></p> <p><a target="_blank" rel="noopener noreferrer" href="http://www.osti.gov/pages">DOE PAGES</a></p> <p>Letscher, R. T.; Moore, J. K.; Teng, Y. -C.; ...</p> <p>2015-01-12</p> <p>Dissolved organic matter (DOM) plays an important role in the ocean's biological carbon pump by providing an advective/mixing pathway for ~ 20% of export production. DOM is known to have a stoichiometry depleted in nitrogen (N) and phosphorus (P) compared to the particulate organic matter pool, a fact that is often omitted from biogeochemical ocean general circulation models. However the variable C : N : P stoichiometry of DOM becomes important when quantifying carbon export from the upper ocean and linking the nutrient cycles of N and P with that of carbon. Here we utilize recent advances in DOM observationalmore » data coverage and offline tracer-modeling techniques to objectively constrain the variable production and remineralization rates of the DOM C : N : P pools in a simple biogeochemical-ocean model of DOM cycling. The optimized DOM cycling parameters are then incorporated within the Biogeochemical Elemental Cycling (BEC) component of the Community Earth System Model (CESM) and validated against the compilation of marine DOM observations. The optimized BEC simulation including variable DOM C : N : P cycling was found to better reproduce the observed DOM spatial gradients than simulations that used the canonical Redfield ratio. Global annual average export of dissolved organic C, N, and P below 100 m was found to be 2.28 Pg C yr -1 (143 Tmol C yr -1, 16.4 Tmol N yr -1, and 1 Tmol P yr -1, respectively, with an average export C : N : P stoichiometry of 225 : 19 : 1 for the semilabile (degradable) DOM pool. Dissolved organic carbon (DOC) export contributed ~ 25% of the combined organic C export to depths greater than 100 m.« less</p> </li> <li> <p><a target="_blank" rel="noopener noreferrer" onclick="trackOutboundLink('https://www.ncbi.nlm.nih.gov/pubmed/27897399','PUBMED'); return false;" href="https://www.ncbi.nlm.nih.gov/pubmed/27897399"><span>Density Functional Theory Research into the Reduction Mechanism for the Solvent/Additive in a Sodium-Ion Battery.</span></a></p> <p><a target="_blank" rel="noopener noreferrer" href="https://www.ncbi.nlm.nih.gov/entrez/query.fcgi?DB=pubmed">PubMed</a></p> <p>Liu, Qi; Mu, Daobin; Wu, Borong; Wang, Lei; Gai, Liang; Wu, Feng</p> <p>2017-02-22</p> <p>The solid-electrolyte interface (SEI) film in a sodium-ion battery is closely related to capacity fading and cycling stability of the battery. However, there are few studies on the SEI film of sodium-ion batteries and the mechanism of SEI film formation is unclear. The mechanism for the reduction of ethylene carbonate (EC), propylene carbonate (PC), vinylene carbonate (VC), ethylene sulfite (ES), 1,3-propylene sulfite (PS), and fluorinated ethylene carbonate (FEC) is studied by DFT. The reaction activation energies, Gibbs free energies, enthalpies, and structures of the transition states are calculated. It is indicated that VC, ES, and PS additives in the electrolyte are all easier to form organic components in the anode SEI film by one-electron reduction. The priority of one-electron reduction to produce organic SEI components is in the order of VC>PC>EC; two-electron reduction to produce the inorganic Na 2 CO 3 component is different and follows the order of EC>PC>VC. Two-electron reduction for sulfites ES and PS to form inorganic Na 2 SO 3 is harder than that of carbonate ester reduction. It is also suggested that the one- and two-electron reductive decomposition pathway for FEC is more feasible to produce inorganic NaF components. © 2017 Wiley-VCH Verlag GmbH & Co. KGaA, Weinheim.</p> </li> <li> <p><a target="_blank" rel="noopener noreferrer" onclick="trackOutboundLink('http://adsabs.harvard.edu/abs/2017GMD....10.2567L','NASAADS'); return false;" href="http://adsabs.harvard.edu/abs/2017GMD....10.2567L"><span>The carbon cycle in the Australian Community Climate and Earth System Simulator (ACCESS-ESM1) - Part 1: Model description and pre-industrial simulation</span></a></p> <p><a target="_blank" rel="noopener noreferrer" href="http://adsabs.harvard.edu/abstract_service.html">NASA Astrophysics Data System (ADS)</a></p> <p>Law, Rachel M.; Ziehn, Tilo; Matear, Richard J.; Lenton, Andrew; Chamberlain, Matthew A.; Stevens, Lauren E.; Wang, Ying-Ping; Srbinovsky, Jhan; Bi, Daohua; Yan, Hailin; Vohralik, Peter F.</p> <p>2017-07-01</p> <p>Earth system models (ESMs) that incorporate carbon-climate feedbacks represent the present state of the art in climate modelling. Here, we describe the Australian Community Climate and Earth System Simulator (ACCESS)-ESM1, which comprises atmosphere (UM7.3), land (CABLE), ocean (MOM4p1), and sea-ice (CICE4.1) components with OASIS-MCT coupling, to which ocean and land carbon modules have been added. The land carbon model (as part of CABLE) can optionally include both nitrogen and phosphorous limitation on the land carbon uptake. The ocean carbon model (WOMBAT, added to MOM) simulates the evolution of phosphate, oxygen, dissolved inorganic carbon, alkalinity and iron with one class of phytoplankton and zooplankton. We perform multi-centennial pre-industrial simulations with a fixed atmospheric CO2 concentration and different land carbon model configurations (prescribed or prognostic leaf area index). We evaluate the equilibration of the carbon cycle and present the spatial and temporal variability in key carbon exchanges. Simulating leaf area index results in a slight warming of the atmosphere relative to the prescribed leaf area index case. Seasonal and interannual variations in land carbon exchange are sensitive to whether leaf area index is simulated, with interannual variations driven by variability in precipitation and temperature. We find that the response of the ocean carbon cycle shows reasonable agreement with observations. While our model overestimates surface phosphate values, the global primary productivity agrees well with observations. Our analysis highlights some deficiencies inherent in the carbon models and where the carbon simulation is negatively impacted by known biases in the underlying physical model and consequent limits on the applicability of this model version. We conclude the study with a brief discussion of key developments required to further improve the realism of our model simulation.</p> </li> <li> <p><a target="_blank" rel="noopener noreferrer" onclick="trackOutboundLink('http://adsabs.harvard.edu/abs/2014JNR....16.2732Z','NASAADS'); return false;" href="http://adsabs.harvard.edu/abs/2014JNR....16.2732Z"><span>Synthesis of porous carbon/silica nanostructured microfiber with ultrahigh surface area</span></a></p> <p><a target="_blank" rel="noopener noreferrer" href="http://adsabs.harvard.edu/abstract_service.html">NASA Astrophysics Data System (ADS)</a></p> <p>Zhou, Dan; Dong, Yan; Cui, Liru; Lin, Huiming; Qu, Fengyu</p> <p>2014-12-01</p> <p>Carbon/silica-nanostructured microfibers were synthesized via electrospinning method using phenol-formaldehyde resin and tetraethyl orthosilicate as carbon and silica precursor with triblock copolymer Pluronic P123 as soft template. The prepared samples show uniform microfiber structure with 1 μm in diameter and dozens of microns in length. Additionally, the mesopores in the material is about 2-6 nm. When the silica component was removed by HF, the porous carbon microfibers (PCMFs) were obtained. In addition, after the carbon/silica composites were calcined in air, the porous silica microfibers (PSiMFs) were obtained, revealing the converse porous nanostructure as PCMFs. It is a simple way to prepare PCMFs and PSiMFs with silica and carbon as the template to each other. Additionally, PCMFs possess an ultrahigh specific surface area (2,092 m2 g-1) and large pore volume. The electrochemical performance of the prepared PCMF material was investigated in 6.0 M KOH electrolyte. The PCMF electrode exhibits a high specific capacitance (252 F g-1 at 0.5 A g-1). Then, superior cycling stability (97 % retention after 4,000 cycles) mainly is due to its unique nanostructure.</p> </li> <li> <p><a target="_blank" rel="noopener noreferrer" onclick="trackOutboundLink('https://www.ncbi.nlm.nih.gov/pubmed/20879549','PUBMED'); return false;" href="https://www.ncbi.nlm.nih.gov/pubmed/20879549"><span>[Effects of climate change on forest soil organic carbon storage: a review].</span></a></p> <p><a target="_blank" rel="noopener noreferrer" href="https://www.ncbi.nlm.nih.gov/entrez/query.fcgi?DB=pubmed">PubMed</a></p> <p>Zhou, Xiao-yu; Zhang, Cheng-yi; Guo, Guang-fen</p> <p>2010-07-01</p> <p>Forest soil organic carbon is an important component of global carbon cycle, and the changes of its accumulation and decomposition directly affect terrestrial ecosystem carbon storage and global carbon balance. Climate change would affect the photosynthesis of forest vegetation and the decomposition and transformation of forest soil organic carbon, and further, affect the storage and dynamics of organic carbon in forest soils. Temperature, precipitation, atmospheric CO2 concentration, and other climatic factors all have important influences on the forest soil organic carbon storage. Understanding the effects of climate change on this storage is helpful to the scientific management of forest carbon sink, and to the feasible options for climate change mitigation. This paper summarized the research progress about the distribution of organic carbon storage in forest soils, and the effects of elevated temperature, precipitation change, and elevated atmospheric CO2 concentration on this storage, with the further research subjects discussed.</p> </li> <li> <p><a target="_blank" rel="noopener noreferrer" onclick="trackOutboundLink('http://adsabs.harvard.edu/abs/2013AGUFM.B33N..07B','NASAADS'); return false;" href="http://adsabs.harvard.edu/abs/2013AGUFM.B33N..07B"><span>Redesigning Urban Carbon Cycles: from Waste Stream to Commodity</span></a></p> <p><a target="_blank" rel="noopener noreferrer" href="http://adsabs.harvard.edu/abstract_service.html">NASA Astrophysics Data System (ADS)</a></p> <p>Brabander, D. J.; Fitzstevens, M. G.</p> <p>2013-12-01</p> <p>While there has been extensive research on the global scale to quantify the fluxes and reservoirs of carbon for predictive climate change models, comparably little attention has been focused on carbon cycles in the built environment. The current management of urban carbon cycles presents a major irony: while cities produce tremendous fluxes of organic carbon waste, their populations are dependent on imported carbon because most urban have limited access to locally sourced carbon. The persistence of outdated management schemes is in part due to the fact that reimagining the handling of urban carbon waste streams requires a transdisciplinary approach. Since the end of the 19th century, U.S. cities have generally relied on the same three options for managing organic carbon waste streams: burn it, bury it, or dilute it. These options still underpin the framework for today's design and management strategies for handling urban carbon waste. We contend that urban carbon management systems for the 21st century need to be scalable, must acknowledge how climate modulates the biogeochemical cycling of urban carbon, and should carefully factor local political and cultural values. Urban waste carbon is a complex matrix ranging from wastewater biosolids to municipal compost. Our first goal in designing targeted and efficient urban carbon management schemes has been examining approaches for categorizing and geochemically fingerprinting these matrices. To date we have used a combination of major and trace element ratio analysis and bulk matrix characteristics, such as pH, density, and loss on ignition, to feed multivariable statistical analysis in order to identify variables that are effective tracers for each waste stream. This approach was initially developed for Boston, MA, US, in the context of identifying components of municipal compost streams that were responsible for increasing the lead inventory in the final product to concentrations that no longer permitted its use in supporting urban agriculture. We are now extending this approach to additional large U.S. and European urban centers where different philosophical and technological approaches to managing urban waste carbon have resulted in a range of infrastructures, from highly distributed systems (Germany) to centralized mega facilities (London). Ultimately, this research will lead to a decision-making matrix model that will permit cities to customize their urban carbon waste stream facilities and transform this waste into a usable commodity.</p> </li> <li> <p><a target="_blank" rel="noopener noreferrer" onclick="trackOutboundLink('https://www.ncbi.nlm.nih.gov/pubmed/25385632','PUBMED'); return false;" href="https://www.ncbi.nlm.nih.gov/pubmed/25385632"><span>Hidden cycle of dissolved organic carbon in the deep ocean.</span></a></p> <p><a target="_blank" rel="noopener noreferrer" href="https://www.ncbi.nlm.nih.gov/entrez/query.fcgi?DB=pubmed">PubMed</a></p> <p>Follett, Christopher L; Repeta, Daniel J; Rothman, Daniel H; Xu, Li; Santinelli, Chiara</p> <p>2014-11-25</p> <p>Marine dissolved organic carbon (DOC) is a large (660 Pg C) reactive carbon reservoir that mediates the oceanic microbial food web and interacts with climate on both short and long timescales. Carbon isotopic content provides information on the DOC source via δ(13)C and age via Δ(14)C. Bulk isotope measurements suggest a microbially sourced DOC reservoir with two distinct components of differing radiocarbon age. However, such measurements cannot determine internal dynamics and fluxes. Here we analyze serial oxidation experiments to quantify the isotopic diversity of DOC at an oligotrophic site in the central Pacific Ocean. Our results show diversity in both stable and radio isotopes at all depths, confirming DOC cycling hidden within bulk analyses. We confirm the presence of isotopically enriched, modern DOC cocycling with an isotopically depleted older fraction in the upper ocean. However, our results show that up to 30% of the deep DOC reservoir is modern and supported by a 1 Pg/y carbon flux, which is 10 times higher than inferred from bulk isotope measurements. Isotopically depleted material turns over at an apparent time scale of 30,000 y, which is far slower than indicated by bulk isotope measurements. These results are consistent with global DOC measurements and explain both the fluctuations in deep DOC concentration and the anomalous radiocarbon values of DOC in the Southern Ocean. Collectively these results provide an unprecedented view of the ways in which DOC moves through the marine carbon cycle.</p> </li> <li> <p><a target="_blank" rel="noopener noreferrer" onclick="trackOutboundLink('https://www.pubmedcentral.nih.gov/articlerender.fcgi?tool=pmcentrez&artid=4250131','PMC'); return false;" href="https://www.pubmedcentral.nih.gov/articlerender.fcgi?tool=pmcentrez&artid=4250131"><span>Hidden cycle of dissolved organic carbon in the deep ocean</span></a></p> <p><a target="_blank" rel="noopener noreferrer" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?DB=pmc">PubMed Central</a></p> <p>Follett, Christopher L.; Repeta, Daniel J.; Rothman, Daniel H.; Xu, Li; Santinelli, Chiara</p> <p>2014-01-01</p> <p>Marine dissolved organic carbon (DOC) is a large (660 Pg C) reactive carbon reservoir that mediates the oceanic microbial food web and interacts with climate on both short and long timescales. Carbon isotopic content provides information on the DOC source via δ13C and age via Δ14C. Bulk isotope measurements suggest a microbially sourced DOC reservoir with two distinct components of differing radiocarbon age. However, such measurements cannot determine internal dynamics and fluxes. Here we analyze serial oxidation experiments to quantify the isotopic diversity of DOC at an oligotrophic site in the central Pacific Ocean. Our results show diversity in both stable and radio isotopes at all depths, confirming DOC cycling hidden within bulk analyses. We confirm the presence of isotopically enriched, modern DOC cocycling with an isotopically depleted older fraction in the upper ocean. However, our results show that up to 30% of the deep DOC reservoir is modern and supported by a 1 Pg/y carbon flux, which is 10 times higher than inferred from bulk isotope measurements. Isotopically depleted material turns over at an apparent time scale of 30,000 y, which is far slower than indicated by bulk isotope measurements. These results are consistent with global DOC measurements and explain both the fluctuations in deep DOC concentration and the anomalous radiocarbon values of DOC in the Southern Ocean. Collectively these results provide an unprecedented view of the ways in which DOC moves through the marine carbon cycle. PMID:25385632</p> </li> <li> <p><a target="_blank" rel="noopener noreferrer" onclick="trackOutboundLink('http://adsabs.harvard.edu/abs/2017AGUFMPP13E..08H','NASAADS'); return false;" href="http://adsabs.harvard.edu/abs/2017AGUFMPP13E..08H"><span>A case of the tail wagging the dog? Reverse weathering and Earth's CO2 thermostat.</span></a></p> <p><a target="_blank" rel="noopener noreferrer" href="http://adsabs.harvard.edu/abstract_service.html">NASA Astrophysics Data System (ADS)</a></p> <p>Higgins, J. A.</p> <p>2017-12-01</p> <p>Feedbacks between climate, the global carbon cycle, and the chemistry of seawater stabilize Earth's surface temperature on geologic timescales and are likely responsible for its habitability over billions of years of Earth history. The most important component of the geologic carbon cycle is the precipitation and burial of carbonate sediments. The amount of carbonate sediment produced depends, in turn, on the alkalinity generated during silicate weathering less the amount consumed during the formation of secondary clay minerals both on the continents and in the ocean. In marine enviroments this process, often referred to as reverse weathering, consumes seawater alkalinity (and cations) via reaction with degraded Al-silicate minerals. Because these reactions constitute a sink of seawater alkalinity, changes in the amount of reverse weathering will lead to imbalances between alkalinity sources and sinks. The net effect is that on timescales greater than the timescale of carbonate compensation (< 10 kyr), changes in reverse weathering will lead to changes in the rate of continental silicate weathering through the dependence of continental silicate weathering on atmospheric CO2 and climate. This mechanism is capable of changing rates of continental silicate weathering without changing either the rate of volcanic outgassing or the rate constant for continental silicate weathering (i.e. through mountain-building or the exposure of different rock types) and as a result represents a unique way of modulating the global carbon cycle and Earth's climate on geologic timescales.</p> </li> </ol> <div class="pull-right"> <ul class="pagination"> <li><a href="#" onclick='return showDiv("page_1");'>«</a></li> <li><a href="#" onclick='return showDiv("page_7");'>7</a></li> <li><a href="#" onclick='return showDiv("page_8");'>8</a></li> <li class="active"><span>9</span></li> <li><a href="#" onclick='return showDiv("page_10");'>10</a></li> <li><a href="#" onclick='return showDiv("page_11");'>11</a></li> <li><a href="#" onclick='return showDiv("page_25");'>»</a></li> </ul> </div> </div><!-- col-sm-12 --> </div><!-- row --> </div><!-- page_9 --> <div id="page_10" class="hiddenDiv"> <div class="row"> <div class="col-sm-12"> <div class="pull-right"> <ul class="pagination"> <li><a href="#" onclick='return showDiv("page_1");'>«</a></li> <li><a href="#" onclick='return showDiv("page_8");'>8</a></li> <li><a href="#" onclick='return showDiv("page_9");'>9</a></li> <li class="active"><span>10</span></li> <li><a href="#" onclick='return showDiv("page_11");'>11</a></li> <li><a href="#" onclick='return showDiv("page_12");'>12</a></li> <li><a href="#" onclick='return showDiv("page_25");'>»</a></li> </ul> </div> </div> </div> <div class="row"> <div class="col-sm-12"> <ol class="result-class" start="181"> <li> <p><a target="_blank" rel="noopener noreferrer" onclick="trackOutboundLink('https://cfpub.epa.gov/si/si_public_record_report.cfm?dirEntryId=65336&keyword=Austria&actType=&TIMSType=+&TIMSSubTypeID=&DEID=&epaNumber=&ntisID=&archiveStatus=Both&ombCat=Any&dateBeginCreated=&dateEndCreated=&dateBeginPublishedPresented=&dateEndPublishedPresented=&dateBeginUpdated=&dateEndUpdated=&dateBeginCompleted=&dateEndCompleted=&personID=&role=Any&journalID=&publisherID=&sortBy=revisionDate&count=50','EPA-EIMS'); return false;" href="https://cfpub.epa.gov/si/si_public_record_report.cfm?dirEntryId=65336&keyword=Austria&actType=&TIMSType=+&TIMSSubTypeID=&DEID=&epaNumber=&ntisID=&archiveStatus=Both&ombCat=Any&dateBeginCreated=&dateEndCreated=&dateBeginPublishedPresented=&dateEndPublishedPresented=&dateBeginUpdated=&dateEndUpdated=&dateBeginCompleted=&dateEndCompleted=&personID=&role=Any&journalID=&publisherID=&sortBy=revisionDate&count=50"><span>CO2 AND O3 ALTER PHOTOSYNTHESIS AND WATER VAPOR EXCHANGE FOR PINUS PONDEROSA NEEDLES</span></a></p> <p><a target="_blank" rel="noopener noreferrer" href="http://oaspub.epa.gov/eims/query.page">EPA Science Inventory</a></p> <p></p> <p></p> <p>1. Effects of CO2 and O3 were determined for a key component of ecosystem carbon and water cycling: needle gas exchange (photosynthesis, conductance, transpiration and water use efficiency). The measurements were made on Pinus ponderosa seedlings grown in outdoor, sunlit, mesoc...</p> </li> <li> <p><a target="_blank" rel="noopener noreferrer" onclick="trackOutboundLink('https://www.fs.usda.gov/treesearch/pubs/35559','TREESEARCH'); return false;" href="https://www.fs.usda.gov/treesearch/pubs/35559"><span>Quantifying soil respiration at landscape scales. Chapter 11</span></a></p> <p><a target="_blank" rel="noopener noreferrer" href="http://www.fs.usda.gov/treesearch/">Treesearch</a></p> <p>John B. Bradford; Michael G. Ryan</p> <p>2008-01-01</p> <p>Soil CO2, efflux, or soil respiration, represents a substantial component of carbon cycling in terrestrial ecosystems. Consequently, quantifying soil respiration over large areas and long time periods is an increasingly important goal. However, soil respiration rates vary dramatically in space and time in response to both environmental conditions...</p> </li> <li> <p><a target="_blank" rel="noopener noreferrer" onclick="trackOutboundLink('http://adsabs.harvard.edu/abs/2017AGUFM.H41G1538B','NASAADS'); return false;" href="http://adsabs.harvard.edu/abs/2017AGUFM.H41G1538B"><span>Parameterization of Nitrogen Limitation for a Dynamic Ecohydrological Model: a Case Study from the Luquillo Critical Zone Observatory</span></a></p> <p><a target="_blank" rel="noopener noreferrer" href="http://adsabs.harvard.edu/abstract_service.html">NASA Astrophysics Data System (ADS)</a></p> <p>Bastola, S.; Bras, R. L.</p> <p>2017-12-01</p> <p>Feedbacks between vegetation and the soil nutrient cycle are important in ecosystems where nitrogen limits plant growth, and consequently influences the carbon balance in the plant-soil system. However, many biosphere models do not include such feedbacks, because interactions between carbon and the nitrogen cycle can be complex, and remain poorly understood. In this study we coupled a nitrogen cycle model with an eco-hydrological model by using the concept of carbon cost economics. This concept accounts for different "costs" to the plant of acquiring nitrogen via different pathways. This study builds on tRIBS-VEGGIE, a spatially explicit hydrological model coupled with a model of photosynthesis, stomatal resistance, and energy balance, by combining it with a model of nitrogen recycling. Driven by climate and spatially explicit data of soils, vegetation and topography, the model (referred to as tRIBS-VEGGIE-CN) simulates the dynamics of carbon and nitrogen in the soil-plant system; the dynamics of vegetation; and different components of the hydrological cycle. The tRIBS-VEGGIE-CN is applied in a humid tropical watershed at the Luquillo Critical Zone Observatory (LCZO). The region is characterized by high availability and cycling of nitrogen, high soil respiration rates, and large carbon stocks.We drive the model under contemporary CO2 and hydro-climatic forcing and compare results to a simulation under doubling CO2 and a range of future climate scenarios. The results with parameterization of nitrogen limitation based on carbon cost economics show that the carbon cost of the acquisition of nitrogen is 14% of the net primary productivity (NPP) and the N uptake cost for different pathways vary over a large range depending on leaf nitrogen content, turnover rates of carbon in soil and nitrogen cycling processes. Moreover, the N fertilization simulation experiment shows that the application of N fertilizer does not significantly change the simulated NPP. Furthermore, an experiment with doubling of the CO2 concentration level shows a significant increase of the NPP and turnover of plant tissues. The simulation with future climate scenarios shows consistent decrease in NPP but the uncertainties in projected NPP arising from selection of climate model and scenario is large.</p> </li> <li> <p><a target="_blank" rel="noopener noreferrer" onclick="trackOutboundLink('http://adsabs.harvard.edu/abs/2017AGUFMGC24G..08S','NASAADS'); return false;" href="http://adsabs.harvard.edu/abs/2017AGUFMGC24G..08S"><span>Integrated model-experimental framework to assess carbon cycle components in disturbed mountainous terrain</span></a></p> <p><a target="_blank" rel="noopener noreferrer" href="http://adsabs.harvard.edu/abstract_service.html">NASA Astrophysics Data System (ADS)</a></p> <p>Stenzel, J.; Hudiburg, T. W.; Berardi, D.; McNellis, B.; Walsh, E.</p> <p>2017-12-01</p> <p>In forests vulnerable to drought and fire, there is critical need for in situ carbon and water balance measurements that can be integrated with earth system modeling to predict climate feedbacks. Model development can be improved by measurements that inform a mechanistic understanding of the component fluxes of net carbon uptake (i.e., NPP, autotrophic and heterotrophic respiration) and water use, with specific focus on responses to climate and disturbance. By integrating novel field-based instrumental technology, existing datasets, and state-of-the-art earth system modeling, we are attempting to 1) quantify the spatial and temporal impacts of forest thinning on regional biogeochemical cycling and climate 2) evaluate the impact of forest thinning on forest resilience to drought and disturbance in the Northern Rockies ecoregion. The combined model-experimental framework enables hypothesis testing that would otherwise be impossible because the use of new in situ high temporal resolution field technology allows for research in remote and mountainous terrains that have been excluded from eddy-covariance techniques. Our preliminary work has revealed some underlying difficulties with the new instrumentation that has led to new ideas and modified methods to correctly measure the component fluxes. Our observations of C balance following the thinning operations indicate that the recovery period (source to sink) is longer than hypothesized. Finally, we have incorporated a new plant functional type parameterization for Northern Rocky mixed-conifer into our simulation modeling using regional and site observations.</p> </li> <li> <p><a target="_blank" rel="noopener noreferrer" onclick="trackOutboundLink('https://www.osti.gov/servlets/purl/1236729','SCIGOV-STC'); return false;" href="https://www.osti.gov/servlets/purl/1236729"><span>Coupling a Supercritical Carbon Dioxide Brayton Cycle to a Helium-Cooled Reactor.</span></a></p> <p><a target="_blank" rel="noopener noreferrer" href="http://www.osti.gov/search">DOE Office of Scientific and Technical Information (OSTI.GOV)</a></p> <p>Middleton, Bobby; Pasch, James Jay; Kruizenga, Alan Michael</p> <p>2016-01-01</p> <p>This report outlines the thermodynamics of a supercritical carbon dioxide (sCO 2) recompression closed Brayton cycle (RCBC) coupled to a Helium-cooled nuclear reactor. The baseline reactor design for the study is the AREVA High Temperature Gas-Cooled Reactor (HTGR). Using the AREVA HTGR nominal operating parameters, an initial thermodynamic study was performed using Sandia's deterministic RCBC analysis program. Utilizing the output of the RCBC thermodynamic analysis, preliminary values of reactor power and of Helium flow rate through the reactor were calculated in Sandia's HelCO 2 code. Some research regarding materials requirements was then conducted to determine aspects of corrosion related tomore » both Helium and to sCO 2 , as well as some mechanical considerations for pressures and temperatures that will be seen by the piping and other components. This analysis resulted in a list of materials-related research items that need to be conducted in the future. A short assessment of dry heat rejection advantages of sCO 2> Brayton cycles was also included. This assessment lists some items that should be investigated in the future to better understand how sCO 2 Brayton cycles and nuclear can maximally contribute to optimizing the water efficiency of carbon free power generation« less</p> </li> <li> <p><a target="_blank" rel="noopener noreferrer" onclick="trackOutboundLink('https://www.ncbi.nlm.nih.gov/pubmed/20586479','PUBMED'); return false;" href="https://www.ncbi.nlm.nih.gov/pubmed/20586479"><span>Design and synthesis of hierarchical MnO2 nanospheres/carbon nanotubes/conducting polymer ternary composite for high performance electrochemical electrodes.</span></a></p> <p><a target="_blank" rel="noopener noreferrer" href="https://www.ncbi.nlm.nih.gov/entrez/query.fcgi?DB=pubmed">PubMed</a></p> <p>Hou, Ye; Cheng, Yingwen; Hobson, Tyler; Liu, Jie</p> <p>2010-07-14</p> <p>For efficient use of metal oxides, such as MnO(2) and RuO(2), in pseudocapacitors and other electrochemical applications, the poor conductivity of the metal oxide is a major problem. To tackle the problem, we have designed a ternary nanocomposite film composed of metal oxide (MnO(2)), carbon nanotube (CNT), and conducting polymer (CP). Each component in the MnO(2)/CNT/CP film provides unique and critical function to achieve optimized electrochemical properties. The electrochemical performance of the film is evaluated by cyclic voltammetry, and constant-current charge/discharge cycling techniques. Specific capacitance (SC) of the ternary composite electrode can reach 427 F/g. Even at high mass loading and high concentration of MnO(2) (60%), the film still showed SC value as high as 200 F/g. The electrode also exhibited excellent charge/discharge rate and good cycling stability, retaining over 99% of its initial charge after 1000 cycles. The results demonstrated that MnO(2) is effectively utilized with assistance of other components (fFWNTs and poly(3,4-ethylenedioxythiophene)-poly(styrenesulfonate) in the electrode. Such ternary composite is very promising for the next generation high performance electrochemical supercapacitors.</p> </li> <li> <p><a target="_blank" rel="noopener noreferrer" onclick="trackOutboundLink('http://adsabs.harvard.edu/abs/2016QSRv..137...15B','NASAADS'); return false;" href="http://adsabs.harvard.edu/abs/2016QSRv..137...15B"><span>Comparative carbon cycle dynamics of the present and last interglacial</span></a></p> <p><a target="_blank" rel="noopener noreferrer" href="http://adsabs.harvard.edu/abstract_service.html">NASA Astrophysics Data System (ADS)</a></p> <p>Brovkin, Victor; Brücher, Tim; Kleinen, Thomas; Zaehle, Sönke; Joos, Fortunat; Roth, Raphael; Spahni, Renato; Schmitt, Jochen; Fischer, Hubertus; Leuenberger, Markus; Stone, Emma J.; Ridgwell, Andy; Chappellaz, Jérôme; Kehrwald, Natalie; Barbante, Carlo; Blunier, Thomas; Dahl Jensen, Dorthe</p> <p>2016-04-01</p> <p>Changes in temperature and carbon dioxide during glacial cycles recorded in Antarctic ice cores are tightly coupled. However, this relationship does not hold for interglacials. While climate cooled towards the end of both the last (Eemian) and present (Holocene) interglacials, CO2 remained stable during the Eemian while rising in the Holocene. We identify and review twelve biogeochemical mechanisms of terrestrial (vegetation dynamics and CO2 fertilization, land use, wildfire, accumulation of peat, changes in permafrost carbon, subaerial volcanic outgassing) and marine origin (changes in sea surface temperature, carbonate compensation to deglaciation and terrestrial biosphere regrowth, shallow-water carbonate sedimentation, changes in the soft tissue pump, and methane hydrates), which potentially may have contributed to the CO2 dynamics during interglacials but which remain not well quantified. We use three Earth System Models (ESMs) of intermediate complexity to compare effects of selected mechanisms on the interglacial CO2 and δ13CO2 changes, focusing on those with substantial potential impacts: namely carbonate sedimentation in shallow waters, peat growth, and (in the case of the Holocene) human land use. A set of specified carbon cycle forcings could qualitatively explain atmospheric CO2 dynamics from 8 ka BP to the pre-industrial. However, when applied to Eemian boundary conditions from 126 to 115 ka BP, the same set of forcings led to disagreement with the observed direction of CO2 changes after 122 ka BP. This failure to simulate late-Eemian CO2 dynamics could be a result of the imposed forcings such as prescribed CaCO3 accumulation and/or an incorrect response of simulated terrestrial carbon to the surface cooling at the end of the interglacial. These experiments also reveal that key natural processes of interglacial CO2 dynamics - shallow water CaCO3 accumulation, peat and permafrost carbon dynamics - are not well represented in the current ESMs. Global-scale modeling of these long-term carbon cycle components started only in the last decade, and uncertainty in parameterization of these mechanisms is a main limitation in the successful modeling of interglacial CO2 dynamics.</p> </li> <li> <p><a target="_blank" rel="noopener noreferrer" onclick="trackOutboundLink('http://hdl.handle.net/2060/20080039566','NASA-TRS'); return false;" href="http://hdl.handle.net/2060/20080039566"><span>Eastern U.S. Continental Shelf Carbon Budget: Integrating Models,Data Assimilation, and Analysis</span></a></p> <p><a target="_blank" rel="noopener noreferrer" href="http://ntrs.nasa.gov/search.jsp">NASA Technical Reports Server (NTRS)</a></p> <p>Hofmann, Eileen; Mannino, Antonio; McClain, Charles R.</p> <p>2007-01-01</p> <p>The U.S. East Coast Continental Shelf (USECoS) project was initiated in 2004 with the overall goal of developing carbon budgets for Mid-Atlantic and South Atlantic regions of the eastern U.S. coast. We addressed this goal through a series of specific research questions that were designed to understand carbon inputs and fates in the two regions, dominant food web pathways for carbon cycling, and similarities/differences in carbon cycling in the two continental shelf systems. The USECoS project represents a major effort to simultaneously synthesize and integrate diverse data sets, field measurements, models, and modeling approaches. We expect that the type of approach taken here will result in more insight than would be possible if each component of the program moved forward independently. The primary significance of this project is in providing a strong quantitative basis for the development of future observational and modeling studies of carbon budgets of continental shelf systems. A strong aspect of the USECoS project is the integration of modeling and extensive physical, chemical, and biological data sets, which provides an opportunity for modeling and data analyses to inform one another from the outset. This research is particularly germane to NASA's carbon cycle research focus and coastal research initiative and the U.S. Climate Change Research Program, all of which support the goals of the North American Carbon Program. We highlight primary approaches that have been used, and some of the challenges and results that have come from interactions among our team of investigators. The global scale and interdisciplinary nature of the science questions that we now face in Earth Science are such that integrated teams of investigators are needed to address them.</p> </li> <li> <p><a target="_blank" rel="noopener noreferrer" onclick="trackOutboundLink('https://www.osti.gov/servlets/purl/1358349','SCIGOV-STC'); return false;" href="https://www.osti.gov/servlets/purl/1358349"><span>Corrosion of Structural Materials for Advanced Supercritical Carbon- Dioxide Brayton Cycle</span></a></p> <p><a target="_blank" rel="noopener noreferrer" href="http://www.osti.gov/search">DOE Office of Scientific and Technical Information (OSTI.GOV)</a></p> <p>Sridharan, Kumar</p> <p></p> <p>The supercritical carbon-dioxide (referred to as SC-CO 2 hereon) Brayton cycle is being considered for power conversion systems for a number of nuclear reactor concepts, including the sodium fast reactor (SFR), fluoride saltcooled high temperature reactor (FHR), and high temperature gas reactor (HTGR), and several types of small modular reactors (SMR). The SC-CO 2 direct cycle gas fast reactor has also been recently proposed. The SC-CO 2 Brayton cycle (discussed in Chapter 1) provides higher efficiencies compared to the Rankine steam cycle due to less compression work stemming from higher SC-CO 2 densities, and allows for smaller components size, fewermore » components, and simpler cycle layout. For example, in the case of a SFR using a SC-CO 2 Brayton cycle instead of a steam cycle would also eliminate the possibility of sodium-water interactions. The SC-CO 2 cycle has a higher efficiency than the helium Brayton cycle, with the additional advantage of being able to operate at lower temperatures and higher pressures. In general, the SC-CO 2 Brayton cycle is well-suited for any type of nuclear reactor (including SMR) with core outlet temperature above ~ 500°C in either direct or indirect versions. In all the above applications, materials corrosion in high temperature SC-CO 2 is an important consideration, given their expected lifetimes of 20 years or longer. Our discussions with National Laboratories and private industry early on in this project indicated materials corrosion to be one of the significant gaps in the implementation of SC-CO 2 Brayton cycle. Corrosion can lead to a loss of effective load-bearing wall thickness of a component and can potentially lead to the generation of oxide particulate debris which can lead to three-body wear in turbomachinery components. Another environmental degradation effect that is rather unique to CO 2 environment is the possibility for simultaneous occurrence of carburization during oxidation of the material. Carburization can potentially lead to embrittlement of structural alloys in SC-CO 2 Brayton cycle. An important consideration in regards to corrosion is that the temperatures can vary widely across the various sections of the SC-CO 2 Brayton cycle, from room temperature to 750°C, with even higher temperatures being desirable for higher efficiencies. Thus the extent of corrosion and corrosion mechanisms in various components and SC-CO 2 Brayton cycle will be different, requiring a judicious selection of materials for different sections of the cycle. The goal of this project was to address materials corrosion-related challenges, identify appropriate materials, and advance the body of scientific knowledge in the area of high temperature SC-CO 2 corrosion. The focus was on corrosion of materials in SC-CO 2 environment in the temperature range of 450°C to 750°C at a pressure of 2900 psi for exposure duration for up to 1000 hours. The Table below lists the materials tested in the project. The materials were selected based on their high temperature strength, their code certification status, commercial availabilities, and their prior or current usage in the nuclear reactor industry. Additionally, pure Fe, Fe-12%Cr, and Ni-22%Cr were investigated as simple model materials to more clearly understand corrosion mechanisms. This first phase of the project involved testing in research grade SC-CO 2 (99.999% purity). Specially designed autoclaves with high fidelity temperature, pressure, and flow control capabilities were built or modified for this project.« less</p> </li> <li> <p><a target="_blank" rel="noopener noreferrer" onclick="trackOutboundLink('http://adsabs.harvard.edu/abs/2016Nanos...8.2418Z','NASAADS'); return false;" href="http://adsabs.harvard.edu/abs/2016Nanos...8.2418Z"><span>GO-induced assembly of gelatin toward stacked layer-like porous carbon for advanced supercapacitors</span></a></p> <p><a target="_blank" rel="noopener noreferrer" href="http://adsabs.harvard.edu/abstract_service.html">NASA Astrophysics Data System (ADS)</a></p> <p>Zhang, Xiaomeng; Jiao, Yanqing; Sun, Li; Wang, Lei; Wu, Aiping; Yan, Haijing; Meng, Meichen; Tian, Chungui; Jiang, Baojiang; Fu, Honggang</p> <p>2016-01-01</p> <p>Layer-like nanocarbons with high surface area and good conductivity are promising materials for supercapacitors due to their good ability for effective charge-transfer and mass-transfer. In this paper, stacked layer-like porous carbon containing RGO (reduced graphene oxides) (LPCG) was constructed via the GO-induced assembly of gelatin followed by carbonization and activation processes. Under suitable conditions, LPCG-based materials with a thickness of about 100 nm and a high specific surface area (up to 1476 m2 g-1) could be obtained. In the materials, the closed combination of RGO and porous carbon can be observed, which is favourable for the development of the synergistic effects of both components. The presence of GO can not only enhance the conductivity of LPCG-based materials, but also is essential for the formation of a thin carbon sheet with a stacked structure. Otherwise, the plate-like, non-stacked carbon with a thickness of about 500 nm could be formed in the absence of RGO. The porous structure along with the presence of RGO allows rapid charge-transfer and easy access and diffusion of electrolyte ions. As a result, the materials exhibited a high discharge specific capacitance (455 F g-1 at 0.5 A g-1, 366 F g-1 at 1 A g-1), good rate capability (221 F g-1 at density 30 A g-1) and good cycling stability. In aqueous electrolytes, the energy density could be up to 9.32 W h kg-1 at a relatively low power density of 500 W kg-1 with a good cycling stability (>96% over 5000 cycles). It was found that (1) the rational combination of RGO and porous carbon is essential for enhancing the capacitance performance and improving the cycling stability and (2) the high conductivity is favorable for improving the rate performance of the materials. The LPCG-based materials have extensive potential for practical applications in energy storage and conversion devices.Layer-like nanocarbons with high surface area and good conductivity are promising materials for supercapacitors due to their good ability for effective charge-transfer and mass-transfer. In this paper, stacked layer-like porous carbon containing RGO (reduced graphene oxides) (LPCG) was constructed via the GO-induced assembly of gelatin followed by carbonization and activation processes. Under suitable conditions, LPCG-based materials with a thickness of about 100 nm and a high specific surface area (up to 1476 m2 g-1) could be obtained. In the materials, the closed combination of RGO and porous carbon can be observed, which is favourable for the development of the synergistic effects of both components. The presence of GO can not only enhance the conductivity of LPCG-based materials, but also is essential for the formation of a thin carbon sheet with a stacked structure. Otherwise, the plate-like, non-stacked carbon with a thickness of about 500 nm could be formed in the absence of RGO. The porous structure along with the presence of RGO allows rapid charge-transfer and easy access and diffusion of electrolyte ions. As a result, the materials exhibited a high discharge specific capacitance (455 F g-1 at 0.5 A g-1, 366 F g-1 at 1 A g-1), good rate capability (221 F g-1 at density 30 A g-1) and good cycling stability. In aqueous electrolytes, the energy density could be up to 9.32 W h kg-1 at a relatively low power density of 500 W kg-1 with a good cycling stability (>96% over 5000 cycles). It was found that (1) the rational combination of RGO and porous carbon is essential for enhancing the capacitance performance and improving the cycling stability and (2) the high conductivity is favorable for improving the rate performance of the materials. The LPCG-based materials have extensive potential for practical applications in energy storage and conversion devices. Electronic supplementary information (ESI) available. See DOI: 10.1039/c5nr07857a</p> </li> <li> <p><a target="_blank" rel="noopener noreferrer" onclick="trackOutboundLink('https://www.ncbi.nlm.nih.gov/pubmed/25651812','PUBMED'); return false;" href="https://www.ncbi.nlm.nih.gov/pubmed/25651812"><span>Carbon partitioning in Arabidopsis thaliana is a dynamic process controlled by the plants metabolic status and its circadian clock.</span></a></p> <p><a target="_blank" rel="noopener noreferrer" href="https://www.ncbi.nlm.nih.gov/entrez/query.fcgi?DB=pubmed">PubMed</a></p> <p>Kölling, Katharina; Thalmann, Matthias; Müller, Antonia; Jenny, Camilla; Zeeman, Samuel C</p> <p>2015-10-01</p> <p>Plant growth involves the coordinated distribution of carbon resources both towards structural components and towards storage compounds that assure a steady carbon supply over the complete diurnal cycle. We used (14) CO2 labelling to track assimilated carbon in both source and sink tissues. Source tissues exhibit large variations in carbon allocation throughout the light period. The most prominent change was detected in partitioning towards starch, being low in the morning and more than double later in the day. Export into sink tissues showed reciprocal changes. Fewer and smaller changes in carbon allocation occurred in sink tissues where, in most respects, carbon was partitioned similarly, whether the sink leaf assimilated it through photosynthesis or imported it from source leaves. Mutants deficient in the production or remobilization of leaf starch exhibited major alterations in carbon allocation. Low-starch mutants that suffer from carbon starvation at night allocated much more carbon into neutral sugars and had higher rates of export than the wild type, partly because of the reduced allocation into starch, but also because of reduced allocation into structural components. Moreover, mutants deficient in the plant's circadian system showed considerable changes in their carbon partitioning pattern suggesting control by the circadian clock. © 2015 The Authors. Plant, Cell & Environment published by John Wiley & Sons Ltd.</p> </li> <li> <p><a target="_blank" rel="noopener noreferrer" onclick="trackOutboundLink('https://www.ncbi.nlm.nih.gov/pubmed/23218247','PUBMED'); return false;" href="https://www.ncbi.nlm.nih.gov/pubmed/23218247"><span>Combined effects of EPS and HRT enhanced biofouling on a submerged and hybrid PAC-MF membrane bioreactor.</span></a></p> <p><a target="_blank" rel="noopener noreferrer" href="https://www.ncbi.nlm.nih.gov/entrez/query.fcgi?DB=pubmed">PubMed</a></p> <p>Khan, Mohiuddin Md Taimur; Takizawa, Satoshi; Lewandowski, Zbigniew; Habibur Rahman, M; Komatsu, Kazuhiro; Nelson, Sara E; Kurisu, Futoshi; Camper, Anne K; Katayama, Hiroyuki; Ohgaki, Shinichiro</p> <p>2013-02-01</p> <p>The goal of this study was to quantify and demonstrate the dynamic effects of hydraulic retention time (HRT), organic carbon and various components of extracellular polymeric substances (EPS) produced by microorganisms on the performance of submersed hollow-fiber microfiltration (MF) membrane in a hybrid powdered activated carbon (PAC)-MF membrane bioreactor (MBR). The reactors were operated continuously for 45 days to treat surface (river) water before and after pretreatment using a biofiltration unit. The real-time levels of organic carbon and the major components of EPS including five different carbohydrates (D(+) glucose and D(+) mannose, D(+) galactose, N-acetyl-D-galactosamine and D-galactose, oligosaccharides and L(-) fucose), proteins, and polysaccharides were quantified in the influent water, foulants, and in the bulk phases of different reactors. The presence of PAC extended the filtration cycle and enhanced the organic carbon adsorption and removal more than two fold. Biological filtration improved the filtrate quality and decreased membrane fouling. However, HRT influenced the length of the filtration cycle and had less effect on organic carbon and EPS component removal and/or biodegradation. The abundance of carbohydrates in the foulants on MF surfaces was more than 40 times higher than in the bulk phase, which demonstrates that the accumulation of carbohydrates on membrane surfaces contributed to the increase in transmembrane pressure significantly and PAC was not a potential adsorbent of carbohydrates. The abundance of N-acetyl-d-galactosamine and d-galactose was the highest in the foulants on membranes receiving biofilter-treated river water. Most of the biological fouling compounds were produced inside the reactors due to biodegradation. PAC inside the reactor enhanced the biodegradation of polysaccharides up to 97% and that of proteins by more than 95%. This real-time extensive and novel study demonstrates that the PAC-MF hybrid MBR is a sustainable technology for treating river water. Copyright © 2012 Elsevier Ltd. All rights reserved.</p> </li> <li> <p><a target="_blank" rel="noopener noreferrer" onclick="trackOutboundLink('http://hdl.handle.net/2060/20180000764','NASA-TRS'); return false;" href="http://hdl.handle.net/2060/20180000764"><span>A Study of the Carbon Cycle Using NASA Observations and the GEOS Model</span></a></p> <p><a target="_blank" rel="noopener noreferrer" href="http://ntrs.nasa.gov/search.jsp">NASA Technical Reports Server (NTRS)</a></p> <p>Pawson, Steven; Gelaro, Ron; Ott, Lesley; Putman, Bill; Chatterjee, Abhishek; Koster, Randy; Lee, Eunjee; Oda, Tom; Weir, Brad; Zeng, Fanwei</p> <p>2018-01-01</p> <p>The Goddard Earth Observing System (GEOS) model has been developed in the Global Modeling and Assimilation Office (GMAO) at NASA's Goddard Space Flight Center. From its roots in chemical transport and as a General Circulation Model, the GEOS model has been extended to an Earth System Model based on a modular construction using the Earth System Modeling Framework (ESMF), combining elements developed in house in the GMAO with others that are imported through collaborative research. It is used extensively for research and for product generation, both as a free-running model and as the core of the GMAO's data assimilation system. In recent years, the GMAO's modeling and assimilation efforts have been strongly supported by Piers Sellers, building on both his earlier legacy as an observationally oriented model developer and his post-astronaut career as a dynamic leader into new territory. Piers' long-standing interest in the carbon cycle and the combination of models with observations motivates this presentation, which will focus on the representation of the carbon cycle in the GEOS Earth System Model. Examples will include: (i) the progression from specified land-atmosphere surface fluxes to computations with an interactive model component (Catchment-CN), along with constraints on vegetation distributions using satellite observations; (ii) the use of high-resolution satellite observations to constrain human-generated inputs to the atmosphere; (iii) studies of the consistency of the observed atmospheric carbon dioxide concentrations with those in the model simulations. The presentation will focus on year-to-year variations in elements of the carbon cycle, specifically on how the observations can inform the representation of mechanisms in the model and lead to integrity in global carbon dioxide simulations. Further, applications of the GEOS model to the planning of new carbon-climate observations will be addressed, as an example of the work that was strongly supported by Piers in the last months of his leadership of Earth Science at NASA Goddard.</p> </li> <li> <p><a target="_blank" rel="noopener noreferrer" onclick="trackOutboundLink('http://adsabs.harvard.edu/abs/1999AIPC..458.1175C','NASAADS'); return false;" href="http://adsabs.harvard.edu/abs/1999AIPC..458.1175C"><span>Thermo-mechanical cyclic testing of carbon-carbon primary structure for an SSTO vehicle</span></a></p> <p><a target="_blank" rel="noopener noreferrer" href="http://adsabs.harvard.edu/abstract_service.html">NASA Astrophysics Data System (ADS)</a></p> <p>Croop, Harold C.; Leger, Kenneth B.; Lowndes, Holland B.; Hahn, Steven E.; Barthel, Chris A.</p> <p>1999-01-01</p> <p>An advanced carbon-carbon structural component is being experimentally evaluated for use as primary load carrying structure for future single-stage-to-orbit (SSTO) vehicles. The component is a wing torque box section featuring an advanced, three-spar design. This design features 3D-woven, angle-interlock skins, 3D integrally woven spar webs and caps, oxidation inhibited matrix, chemical vapor deposited (CVD) oxidation protection coating, and ceramic matrix composite fasteners. The box spar caps are nested into the skins which, when processed together through the carbon-carbon processing cycle, resulted in monolithic box halves. The box half sections were then joined at the spar web intersections using ceramic matrix composite fasteners. This method of fabrication eliminated fasteners through both the upper and lower skins. Development of the carbon-carbon wing box structure was accomplished in a four phase design and fabrication effort, conducted by Boeing, Information, Space and Defense Systems, Seattle, WA, under contract to the Air Force Research Laboratory (AFRL). The box is now set up for testing and will soon begin cyclic loads testing in the AFRL Structural Test Facility at Wright-Patterson Air Force Base (WPAFB), OH. This paper discusses the latest test setup accomplishments and the results of the pre-cyclic loads testing performed to date.</p> </li> <li> <p><a target="_blank" rel="noopener noreferrer" onclick="trackOutboundLink('http://www.ars.usda.gov/research/publications/publication/?seqNo115=243963','TEKTRAN'); return false;" href="http://www.ars.usda.gov/research/publications/publication/?seqNo115=243963"><span>Global Potential Net Prmary Production Predicted from Vegetation Class, Precipitation, and Temperature</span></a></p> <p><a target="_blank" rel="noopener noreferrer" href="https://www.ars.usda.gov/research/publications/find-a-publication/">USDA-ARS?s Scientific Manuscript database</a></p> <p></p> <p></p> <p>Net Primary Production (NPP), the difference between CO2 fixed by photosynthesis and CO2 lost to autotrophic respiration, is one of the most important components of the carbon cycle. Our goal was to develop a simple regression model to estimate global NPP using climate and land cover data. Approxima...</p> </li> <li> <p><a target="_blank" rel="noopener noreferrer" onclick="trackOutboundLink('http://adsabs.harvard.edu/abs/2016EGUGA..1815535S','NASAADS'); return false;" href="http://adsabs.harvard.edu/abs/2016EGUGA..1815535S"><span>Bony fish and their contribution to marine inorganic carbon cycling</span></a></p> <p><a target="_blank" rel="noopener noreferrer" href="http://adsabs.harvard.edu/abstract_service.html">NASA Astrophysics Data System (ADS)</a></p> <p>Salter, Michael; Perry, Chris; Wilson, Rod; Harborne, Alistair</p> <p>2016-04-01</p> <p>Conventional understanding of the marine inorganic carbon cycle holds that CaCO3 (mostly as low Mg-calcite and aragonite) precipitates in the upper reaches of the ocean and sinks to a point where it either dissolves or is deposited as sediment. Thus, it plays a key role controlling the distribution of DIC in the oceans and in regulating their capacity to absorb atmospheric CO2. However, several aspects of this cycle remain poorly understood and have long perplexed oceanographers, such as the positive alkalinity anomaly observed in the upper water column of many of the world's oceans, above the aragonite and calcite saturation horizons. This anomaly would be explained by extensive dissolution of a carbonate phase more soluble than low Mg-calcite or aragonite, but major sources for such phases remain elusive. Here we highlight marine bony fish as a potentially important primary source of this 'missing' high-solubility CaCO3. Precipitation of CaCO3 takes place within the intestines of all marine bony fish as part of their normal physiological functioning, and global production models suggest it could account for up to 45 % of total new marine CaCO3 production. Moreover, high Mg-calcite containing >25 % mol% MgCO3 - a more soluble phase than aragonite - is a major component of these precipitates. Thus, fish CaCO3 may at least partially explain the alkalinity anomaly in the upper water column. However, the issue is complicated by the fact that carbonate mineralogy actually varies among fish species, with high Mg-calcite (HMC), low Mg-calcite (LMC), aragonite, and amorphous calcium carbonate (ACC) all being common products. Using data from 22 Caribbean fish species, we have generated a novel production model that resolves phase proportions. We evaluate the preservation/dissolution potential of these phases and consider potential implications for marine inorganic carbon cycling. In addition, we consider the dramatic changes in fish biomass structure that have resulted from overfishing throughout the past century, and how these changes could be affecting marine carbon cycling. Given that rising sea surface temperatures and 'ocean acidification' are both predicted to promote increased fish CaCO3 production rates, the role of fish in the marine inorganic carbon cycle could become increasingly important in the future. Consequently, it is conceivable that fish stock management could become an important carbon-regulating service employed in the face of challenges such as climate change mitigation, so it is vital that this role is properly comprehended.</p> </li> <li> <p><a target="_blank" rel="noopener noreferrer" onclick="trackOutboundLink('http://adsabs.harvard.edu/abs/2013AGUFM.B53A0444W','NASAADS'); return false;" href="http://adsabs.harvard.edu/abs/2013AGUFM.B53A0444W"><span>Implementation of diverse tree hydraulics in a land surface model</span></a></p> <p><a target="_blank" rel="noopener noreferrer" href="http://adsabs.harvard.edu/abstract_service.html">NASA Astrophysics Data System (ADS)</a></p> <p>Wolf, A.; Shevliakova, E.; Malyshev, S.; Weng, E.; Pacala, S. W.</p> <p>2013-12-01</p> <p>Increasing attention has been devoted to the occurence of drought kill in forests worldwide. These mortality events are significant disruptions to the terrestrial carbon cycle, but the mechanisms required to represent drought kill are not represented in terrestrial carbon cycle models. In part, this is due to the challenge of representing the diversity of hydraulic strategies, which include stomatal sensitivity to water deficit and woody tissue vulnerability to cavitation at low water potential. In part, this is due to the challenge of representing this boundary value problem numerically, because the hydraulic components determine water potential at the leaf, but the stomatal conductance on the leaf also determines the hydraulic gradients within the plant. This poster will describe the development of a land surface model parameterization of diverse tree hydraulic strategies.</p> </li> <li> <p><a target="_blank" rel="noopener noreferrer" onclick="trackOutboundLink('http://adsabs.harvard.edu/abs/2017AGUFM.H21J1610P','NASAADS'); return false;" href="http://adsabs.harvard.edu/abs/2017AGUFM.H21J1610P"><span>Impact of Seasonal Variability in Water, Plant and Soil Nutrient Dynamics in Agroecosystems</span></a></p> <p><a target="_blank" rel="noopener noreferrer" href="http://adsabs.harvard.edu/abstract_service.html">NASA Astrophysics Data System (ADS)</a></p> <p>Pelak, N. F., III; Revelli, R.; Porporato, A. M.</p> <p>2017-12-01</p> <p>Agroecosystems cover a significant fraction of the Earth's surface, making their water and nutrient cycles a major component of global cycles across spatial and temporal scales. Most agroecosystems experience seasonality via variations in precipitation, temperature, and radiation, in addition to human activities which also occur seasonally, such as fertilization, irrigation, and harvesting. These seasonal drivers interact with the system in complex ways which are often poorly characterized. Crop models, which are widely used for research, decision support, and prediction of crop yields, are among the best tools available to analyze these systems. Though normally constructed as a set of dynamical equations forced by hydroclimatic variability, they are not often analyzed using dynamical systems theory and methods from stochastic ecohydrology. With the goal of developing this viewpoint and thus elucidating the roles of key feedbacks and forcings on system stability and on optimal fertilization and irrigation strategies, we develop a minimal dynamical system which contains the key components of a crop model, coupled to a carbon and nitrogen cycling model, driven by seasonal fluctuations in water and nutrient availability, temperature, and radiation. External drivers include seasonally varying climatic conditions and random rainfall forcing, irrigation and fertilization as well as harvesting. The model is used to analyze the magnitudes and interactions of the effects of seasonality on carbon and nutrient cycles, crop productivity, nutrient export of agroecosystems, and optimal management strategies with reference to productivity, sustainability and profitability. The impact of likely future climate scenarios on these systems is also discussed.</p> </li> <li> <p><a target="_blank" rel="noopener noreferrer" onclick="trackOutboundLink('https://www.pubmedcentral.nih.gov/articlerender.fcgi?tool=pmcentrez&artid=5043302','PMC'); return false;" href="https://www.pubmedcentral.nih.gov/articlerender.fcgi?tool=pmcentrez&artid=5043302"><span>Fossil clam shells reveal unintended carbon cycling consequences of Colorado River management</span></a></p> <p><a target="_blank" rel="noopener noreferrer" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?DB=pmc">PubMed Central</a></p> <p>Auerbach, Daniel A.; Flessa, Karl W.; Flecker, Alexander S.; Dietl, Gregory P.</p> <p>2016-01-01</p> <p>Water management that alters riverine ecosystem processes has strongly influenced deltas and the people who depend on them, but a full accounting of the trade-offs is still emerging. Using palaeoecological data, we document a surprising biogeochemical consequence of water management in the Colorado River basin. Complete allocation and consumptive use of the river's flow has altered the downstream estuarine ecosystem, including the abundance and composition of the mollusc community, an important component in estuarine carbon cycling. In particular, population declines in the endemic Colorado delta clam, Mulinia coloradoensis, from 50--125 individuals m−2 in the pre-dam era to three individuals m−2 today, have likely resulted in a reduction, on the order of 5900–15 000 t C yr−1 (4.1–10.6 mol C m−2 yr−1), in the net carbon emissions associated with molluscs. Although this reduction is large within the estuarine system, it is small in comparison with annual global carbon emissions. Nonetheless, this finding highlights the need for further research into the effects of dams, diversions and reservoirs on the biogeochemistry of deltas and estuaries worldwide, underscoring a present need for integrated water and carbon planning. PMID:27703685</p> </li> <li> <p><a target="_blank" rel="noopener noreferrer" onclick="trackOutboundLink('https://www.ncbi.nlm.nih.gov/pubmed/28559315','PUBMED'); return false;" href="https://www.ncbi.nlm.nih.gov/pubmed/28559315"><span>Historical climate controls soil respiration responses to current soil moisture.</span></a></p> <p><a target="_blank" rel="noopener noreferrer" href="https://www.ncbi.nlm.nih.gov/entrez/query.fcgi?DB=pubmed">PubMed</a></p> <p>Hawkes, Christine V; Waring, Bonnie G; Rocca, Jennifer D; Kivlin, Stephanie N</p> <p>2017-06-13</p> <p>Ecosystem carbon losses from soil microbial respiration are a key component of global carbon cycling, resulting in the transfer of 40-70 Pg carbon from soil to the atmosphere each year. Because these microbial processes can feed back to climate change, understanding respiration responses to environmental factors is necessary for improved projections. We focus on respiration responses to soil moisture, which remain unresolved in ecosystem models. A common assumption of large-scale models is that soil microorganisms respond to moisture in the same way, regardless of location or climate. Here, we show that soil respiration is constrained by historical climate. We find that historical rainfall controls both the moisture dependence and sensitivity of respiration. Moisture sensitivity, defined as the slope of respiration vs. moisture, increased fourfold across a 480-mm rainfall gradient, resulting in twofold greater carbon loss on average in historically wetter soils compared with historically drier soils. The respiration-moisture relationship was resistant to environmental change in field common gardens and field rainfall manipulations, supporting a persistent effect of historical climate on microbial respiration. Based on these results, predicting future carbon cycling with climate change will require an understanding of the spatial variation and temporal lags in microbial responses created by historical rainfall.</p> </li> </ol> <div class="pull-right"> <ul class="pagination"> <li><a href="#" onclick='return showDiv("page_1");'>«</a></li> <li><a href="#" onclick='return showDiv("page_8");'>8</a></li> <li><a href="#" onclick='return showDiv("page_9");'>9</a></li> <li class="active"><span>10</span></li> <li><a href="#" onclick='return showDiv("page_11");'>11</a></li> <li><a href="#" onclick='return showDiv("page_12");'>12</a></li> <li><a href="#" onclick='return showDiv("page_25");'>»</a></li> </ul> </div> </div><!-- col-sm-12 --> </div><!-- row --> </div><!-- page_10 --> <div id="page_11" class="hiddenDiv"> <div class="row"> <div class="col-sm-12"> <div class="pull-right"> <ul class="pagination"> <li><a href="#" onclick='return showDiv("page_1");'>«</a></li> <li><a href="#" onclick='return showDiv("page_9");'>9</a></li> <li><a href="#" onclick='return showDiv("page_10");'>10</a></li> <li class="active"><span>11</span></li> <li><a href="#" onclick='return showDiv("page_12");'>12</a></li> <li><a href="#" onclick='return showDiv("page_13");'>13</a></li> <li><a href="#" onclick='return showDiv("page_25");'>»</a></li> </ul> </div> </div> </div> <div class="row"> <div class="col-sm-12"> <ol class="result-class" start="201"> <li> <p><a target="_blank" rel="noopener noreferrer" onclick="trackOutboundLink('http://adsabs.harvard.edu/abs/2016RSOS....360170S','NASAADS'); return false;" href="http://adsabs.harvard.edu/abs/2016RSOS....360170S"><span>Fossil clam shells reveal unintended carbon cycling consequences of Colorado River management</span></a></p> <p><a target="_blank" rel="noopener noreferrer" href="http://adsabs.harvard.edu/abstract_service.html">NASA Astrophysics Data System (ADS)</a></p> <p>Smith, Jansen A.; Auerbach, Daniel A.; Flessa, Karl W.; Flecker, Alexander S.; Dietl, Gregory P.</p> <p>2016-09-01</p> <p>Water management that alters riverine ecosystem processes has strongly influenced deltas and the people who depend on them, but a full accounting of the trade-offs is still emerging. Using palaeoecological data, we document a surprising biogeochemical consequence of water management in the Colorado River basin. Complete allocation and consumptive use of the river's flow has altered the downstream estuarine ecosystem, including the abundance and composition of the mollusc community, an important component in estuarine carbon cycling. In particular, population declines in the endemic Colorado delta clam, Mulinia coloradoensis, from 50-125 individuals m-2 in the pre-dam era to three individuals m-2 today, have likely resulted in a reduction, on the order of 5900-15 000 t C yr-1 (4.1-10.6 mol C m-2 yr-1), in the net carbon emissions associated with molluscs. Although this reduction is large within the estuarine system, it is small in comparison with annual global carbon emissions. Nonetheless, this finding highlights the need for further research into the effects of dams, diversions and reservoirs on the biogeochemistry of deltas and estuaries worldwide, underscoring a present need for integrated water and carbon planning.</p> </li> <li> <p><a target="_blank" rel="noopener noreferrer" onclick="trackOutboundLink('https://www.pubmedcentral.nih.gov/articlerender.fcgi?tool=pmcentrez&artid=3848262','PMC'); return false;" href="https://www.pubmedcentral.nih.gov/articlerender.fcgi?tool=pmcentrez&artid=3848262"><span>Lignin: Characterization of a Multifaceted Crop Component</span></a></p> <p><a target="_blank" rel="noopener noreferrer" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?DB=pmc">PubMed Central</a></p> <p></p> <p>2013-01-01</p> <p>Lignin is a plant component with important implications for various agricultural disciplines. It confers rigidity to cell walls, and is therefore associated with tolerance to abiotic and biotic stresses and the mechanical stability of plants. In animal nutrition, lignin is considered an antinutritive component of forages as it cannot be readily fermented by rumen microbes. In terms of energy yield from biomass, the role of lignin depends on the conversion process. It contains more gross energy than other cell wall components and therefore confers enhanced heat value in thermochemical processes such as direct combustion. Conversely, it negatively affects biological energy conversion processes such as bioethanol or biogas production, as it inhibits microbial fermentation of the cell wall. Lignin from crop residues plays an important role in the soil organic carbon cycling, as it constitutes a recalcitrant carbon pool affecting nutrient mineralization and carbon sequestration. Due to the significance of lignin in several agricultural disciplines, the modification of lignin content and composition by breeding is becoming increasingly important. Both mapping of quantitative trait loci and transgenic approaches have been adopted to modify lignin in crops. However, breeding goals must be defined considering the conflicting role of lignin in different agricultural disciplines. PMID:24348159</p> </li> <li> <p><a target="_blank" rel="noopener noreferrer" onclick="trackOutboundLink('http://adsabs.harvard.edu/abs/2017AGUFM.B23C2081D','NASAADS'); return false;" href="http://adsabs.harvard.edu/abs/2017AGUFM.B23C2081D"><span>Molecular and Imaging Insights into the Formation of Soil Organic Matter in a Red Pine Rhizosphere</span></a></p> <p><a target="_blank" rel="noopener noreferrer" href="http://adsabs.harvard.edu/abstract_service.html">NASA Astrophysics Data System (ADS)</a></p> <p>Dohnalkova, A.; Tfaily, M.; Smith, A. P.; Chu, R. K.; Crump, A.; Brislawn, C.; Varga, T.; Shi, Z.; Thomashow, L. S.; Harsh, J. B.; Balogh-Brunstad, Z.; Keller, C. K.</p> <p>2017-12-01</p> <p>Microbially-derived carbon inputs to soils play an important role in forming soil organic matter (SOM), but detailed knowledge of basic mechanisms of carbon (C) cycling, such as stabilization of organic C compounds originating from rhizodeposition, is limited. The objective of this study aimed to investigate the stability of rhizosphere-produced carbon components in a model laboratory mesocosm of Pinus resinosa grown in a designed mineral soil mix. We hypothesized that nutrient limitation would cause formation of microbially-produced C constituents that would contribute to SOM stabilization. We focused on the processes of rhizodeposition in the rhizosphere, and we utilized a suite of advanced imaging and molecular techniques to obtain a molecular-level identification of the microbial community and the newly-formed SOM compounds in the rhizosphere and the bulk soil. We considered implications regarding their degree of long-term stability. The microbes in this controlled, nutrient-limited system, without pre-existing organic matter, produced extracellular polymeric substances that formed associations with nutrient-bearing minerals and contributed to the microbial mineral weathering process. Electron microscopy revealed unique ultrastructural residual signatures of biogenic C compounds, and the increased presence of an amorphous organic phase associated with the mineral phase was evidenced by X-ray diffraction. These findings provide insight into the various degrees of stability of microbial SOM products in ecosystems and evidence that the residual biogenic material associated with mineral matrices may be important components in current carbon cycle models.</p> </li> <li> <p><a target="_blank" rel="noopener noreferrer" onclick="trackOutboundLink('https://www.pubmedcentral.nih.gov/articlerender.fcgi?tool=pmcentrez&artid=4066249','PMC'); return false;" href="https://www.pubmedcentral.nih.gov/articlerender.fcgi?tool=pmcentrez&artid=4066249"><span>Lithographically Defined Three-dimensional Pore-patterned Carbon with Nitrogen Doping for High-Performance Ultrathin Supercapacitor Applications</span></a></p> <p><a target="_blank" rel="noopener noreferrer" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?DB=pmc">PubMed Central</a></p> <p>Kang, Da-Young; Moon, Jun Hyuk</p> <p>2014-01-01</p> <p>Supercapacitors that exhibit long cycle lives and fast charge/discharge rates are a promising energy-storage technology for next-generation mobile or wearable electronic systems. A great challenge facing the fabrication of ultrathin supercapacitor components, specifically their porous electrodes, is whether such components can be integrated with the fabrication of electronic devices, i.e., semiconductor fabrication processes. Here, we introduce the lithographic fabrication of micrometre-thick, submicrometre-pore-patterned carbon for supercapacitor electrodes. The pore patterns designed by multi-beam interference lithography and direct carbonisation of the photoresist pattern produced pore-patterned carbon films. A facile doping process was subsequently employed to introduce nitrogen atoms into the carbon, which was intended to further enhance the carbon's capacitive properties. Specifically, during these fabrication steps, we developed an approach that uses a supporting shell on the surface of the pore patterns to maintain their structural integrity. The nitrogen-doped, pore-patterned carbon electrodes exhibited an areal specific capacitance of 32.7 mF/cm2 at 0.5 mA/cm2 when used as supercapacitor electrodes, which is approximately 20 times greater than that of commercially available MWCNT films measured under the same conditions. PMID:24953307</p> </li> <li> <p><a target="_blank" rel="noopener noreferrer" onclick="trackOutboundLink('http://adsabs.harvard.edu/abs/2017AIPC.1850f0001M','NASAADS'); return false;" href="http://adsabs.harvard.edu/abs/2017AIPC.1850f0001M"><span>Techno-economic analysis of supercritical carbon dioxide power blocks</span></a></p> <p><a target="_blank" rel="noopener noreferrer" href="http://adsabs.harvard.edu/abstract_service.html">NASA Astrophysics Data System (ADS)</a></p> <p>Meybodi, Mehdi Aghaei; Beath, Andrew; Gwynn-Jones, Stephen; Veeraragavan, Anand; Gurgenci, Hal; Hooman, Kamel</p> <p>2017-06-01</p> <p>Developing highly efficient power blocks holds the key to enhancing the cost competitiveness of Concentration Solar Thermal (CST) technologies. Supercritical CO2 (sCO2) Brayton cycles have proved promising in providing equivalent or higher cycle efficiency than supercritical or superheated steam cycles at temperatures and scales relevant for Australian CST applications. In this study, a techno-economic methodology is developed using a stochastic approach to determine the ranges for the cost and performance of different components of central receiver power plants utilizing sCO2 power blocks that are necessary to meet the Australian Solar Thermal Initiative (ASTRI) final LCOE target of 12 c/kWh.</p> </li> <li> <p><a target="_blank" rel="noopener noreferrer" onclick="trackOutboundLink('https://ntrs.nasa.gov/search.jsp?R=19860055931&hterms=k-12&qs=Ntx%3Dmode%2Bmatchall%26Ntk%3DAll%26N%3D0%26No%3D90%26Ntt%3Dk-12','NASA-TRS'); return false;" href="https://ntrs.nasa.gov/search.jsp?R=19860055931&hterms=k-12&qs=Ntx%3Dmode%2Bmatchall%26Ntk%3DAll%26N%3D0%26No%3D90%26Ntt%3Dk-12"><span>Carbon isotopic fractionation in heterotrophic microbial metabolism</span></a></p> <p><a target="_blank" rel="noopener noreferrer" href="http://ntrs.nasa.gov/search.jsp">NASA Technical Reports Server (NTRS)</a></p> <p>Blair, N.; Leu, A.; Munoz, E.; Olsen, J.; Kwong, E.; Des Marais, D.</p> <p>1985-01-01</p> <p>Differences in the natural-abundance carbon stable isotopic compositions between products from aerobic cultures of Escherichia coli K-12 were measured. Respired CO2 was 3.4 percent depleted in C-13 relative to the glucose used as the carbon source, whereas the acetate was 12.3 percent enriched in C-13. The acetate C-13 enrichment was solely in the carboxyl group. Even though the total cellular carbon was only 0.6 percent depleted in C-13, intracellular components exhibited a significant isotopic heterogeneity. The protein and lipid fractions were -1.1 and -2.7 percent, respectively. Aspartic and glutamic acids were -1.6 and +2.7 percent, respectively, yet citrate was isotopically identical to the glucose. Probable sites of carbon isotopic fractionation include the enzyme, phosphotransacetylase, and the Krebs cycle.</p> </li> <li> <p><a target="_blank" rel="noopener noreferrer" onclick="trackOutboundLink('http://adsabs.harvard.edu/abs/2016AGUFMGC23K..14F','NASAADS'); return false;" href="http://adsabs.harvard.edu/abs/2016AGUFMGC23K..14F"><span>Carbon fluxes in North American coastal and shelf seas: Current status and trends</span></a></p> <p><a target="_blank" rel="noopener noreferrer" href="http://adsabs.harvard.edu/abstract_service.html">NASA Astrophysics Data System (ADS)</a></p> <p>Fennel, K.; Alin, S. R.; Barbero, L.; Evans, W.; Martin Hernandez-Ayon, J. M.; Hu, X.; Lohrenz, S. E.; Muller-Karger, F. E.; Najjar, R.; Robbins, L. L.; Shadwick, E. H.; Siedlecki, S. A.; Steiner, N.; Turk, D.; Vlahos, P.; Wang, A. Z.</p> <p>2016-12-01</p> <p>Coastal and shelf seas represent an interface between all major components of the global carbon cycle: land, atmosphere, marine sediments and the ocean. Fluxes and transformations of carbon in coastal systems are complex and highly variable in space and time. The First State of the Carbon Cycle Report (http://cdiac.ornl.gov/SOCCR/final.html, Chapter 15, Chavez et al. 2007) concluded that carbon budgets of North American ocean margins were not well quantified because of insufficient observations and the complexity and highly localized spatial variability of coastal carbon dynamics. Since then significant progress has been made through the expansion of carbon observing networks, the implementation of modeling capabilities, and national and international coordination and synthesis activities. We will review the current understanding of coastal carbon fluxes around the North American continent including along the Atlantic and Pacific coasts, the northern Gulf of Mexico, and the North American Arctic region and provide a compilation of regional estimates of air-sea fluxes of CO2. We will discuss generalizable patterns in coastal air-sea CO2 exchange and other carbon fluxes as well as reasons underlying spatial heterogeneity. After providing an overview of the principal modes of carbon export from coastal systems, we will apply these mechanisms to the North American continent, and discuss observed and projected trends of key properties and fluxes. The presentation will illustrate that despite significant advances in capabilities and understanding, large uncertainties remain.</p> </li> <li> <p><a target="_blank" rel="noopener noreferrer" onclick="trackOutboundLink('http://adsabs.harvard.edu/abs/2012AGUFMIN34A..02W','NASAADS'); return false;" href="http://adsabs.harvard.edu/abs/2012AGUFMIN34A..02W"><span>Data Standardization for Carbon Cycle Modeling: Lessons Learned</span></a></p> <p><a target="_blank" rel="noopener noreferrer" href="http://adsabs.harvard.edu/abstract_service.html">NASA Astrophysics Data System (ADS)</a></p> <p>Wei, Y.; Liu, S.; Cook, R. B.; Post, W. M.; Huntzinger, D. N.; Schwalm, C.; Schaefer, K. M.; Jacobson, A. R.; Michalak, A. M.</p> <p>2012-12-01</p> <p>Terrestrial biogeochemistry modeling is a crucial component of carbon cycle research and provides unique capabilities to understand terrestrial ecosystems. The Multi-scale Synthesis and Terrestrial Model Intercomparison Project (MsTMIP) aims to identify key differences in model formulation that drive observed differences in model predictions of biospheric carbon exchange. To do so, the MsTMIP framework provides standardized prescribed environmental driver data and a standard model protocol to facilitate comparisons of modeling results from nearly 30 teams. Model performance is then evaluated against a variety of carbon-cycle related observations (remote sensing, atmospheric, and flux tower-based observations) using quantitative performance measures and metrics in an integrated evaluation framework. As part of this effort, we have harmonized highly diverse and heterogeneous environmental driver data, model outputs, and observational benchmark data sets to facilitate use and analysis by the MsTMIP team. In this presentation, we will describe the lessons learned from this data-intensive carbon cycle research. The data harmonization activity itself can be made more efficient with the consideration of proper tools, version control, workflow management, and collaboration within the whole team. The adoption of on-demand and interoperable protocols (e.g. OPeNDAP and Open Geospatial Consortium) makes data visualization and distribution more flexible. Users can customize and download data in specific spatial extent, temporal period, and different resolutions. The effort to properly organize data in an open and standard format (e.g. Climate & Forecast compatible netCDF) allows the data to be analysed by a dispersed set of researchers more efficiently, and maximizes the longevity and utilization of the data. The lessons learned from this specific experience can benefit efforts by the broader community to leverage diverse data resources more efficiently in scientific research.</p> </li> <li> <p><a target="_blank" rel="noopener noreferrer" onclick="trackOutboundLink('https://www.ncbi.nlm.nih.gov/pubmed/21898102','PUBMED'); return false;" href="https://www.ncbi.nlm.nih.gov/pubmed/21898102"><span>Environmental controls on microbial abundance and activity on the greenland ice sheet: a multivariate analysis approach.</span></a></p> <p><a target="_blank" rel="noopener noreferrer" href="https://www.ncbi.nlm.nih.gov/entrez/query.fcgi?DB=pubmed">PubMed</a></p> <p>Stibal, Marek; Telling, Jon; Cook, Joe; Mak, Ka Man; Hodson, Andy; Anesio, Alexandre M</p> <p>2012-01-01</p> <p>Microbes in supraglacial ecosystems have been proposed to be significant contributors to regional and possibly global carbon cycling, and quantifying the biogeochemical cycling of carbon in glacial ecosystems is of great significance for global carbon flow estimations. Here we present data on microbial abundance and productivity, collected along a transect across the ablation zone of the Greenland ice sheet (GrIS) in summer 2010. We analyse the relationships between the physical, chemical and biological variables using multivariate statistical analysis. Concentrations of debris-bound nutrients increased with distance from the ice sheet margin, as did both cell numbers and activity rates before reaching a peak (photosynthesis) or a plateau (respiration, abundance) between 10 and 20 km from the margin. The results of productivity measurements suggest an overall net autotrophy on the GrIS and support the proposed role of ice sheet ecosystems in carbon cycling as regional sinks of CO(2) and places of production of organic matter that can be a potential source of nutrients for downstream ecosystems. Principal component analysis based on chemical and biological data revealed three clusters of sites, corresponding to three 'glacier ecological zones', confirmed by a redundancy analysis (RDA) using physical data as predictors. RDA using data from the largest 'bare ice zone' showed that glacier surface slope, a proxy for melt water flow, accounted for most of the variation in the data. Variation in the chemical data was fully explainable by the determined physical variables. Abundance of phototrophic microbes and their proportion in the community were identified as significant controls of the carbon cycling-related microbial processes.</p> </li> <li> <p><a target="_blank" rel="noopener noreferrer" onclick="trackOutboundLink('https://www.ncbi.nlm.nih.gov/pubmed/28419976','PUBMED'); return false;" href="https://www.ncbi.nlm.nih.gov/pubmed/28419976"><span>Microbial extracellular enzymes in biogeochemical cycling of ecosystems.</span></a></p> <p><a target="_blank" rel="noopener noreferrer" href="https://www.ncbi.nlm.nih.gov/entrez/query.fcgi?DB=pubmed">PubMed</a></p> <p>Luo, Ling; Meng, Han; Gu, Ji-Dong</p> <p>2017-07-15</p> <p>Extracellular enzymes, primarily produced by microorganisms, affect ecosystem processes because of their essential roles in degradation, transformation and mineralization of organic matter. Extracellular enzymes involved in the cycling of carbon (C), nitrogen (N) and phosphorus (P) have been widely investigated in many different ecosystems, and several enzymes have been recognized as key components in regulating C storage and nutrient cycling. In this review, it was the first time to summarize the specific extracellular enzymes related to C storage and nutrient cycling for better understanding the important role of microbial extracellular enzymes in biogeochemical cycling of ecosystems. Subsequently, ecoenzymatic stoichiometry - the relative ratio of extracellular enzyme, has been reviewed and further provided a new perspective for understanding biogeochemical cycling of ecosystems. Finally, the new insights of using microbial extracellular enzyme in indicating biogeochemical cycling and then protecting ecosystems have been suggested. Copyright © 2017 Elsevier Ltd. All rights reserved.</p> </li> <li> <p><a target="_blank" rel="noopener noreferrer" onclick="trackOutboundLink('http://adsabs.harvard.edu/abs/2017GBioC..31.1704K','NASAADS'); return false;" href="http://adsabs.harvard.edu/abs/2017GBioC..31.1704K"><span>Long-Term Drainage Reduces CO2 Uptake and CH4 Emissions in a Siberian Permafrost Ecosystem</span></a></p> <p><a target="_blank" rel="noopener noreferrer" href="http://adsabs.harvard.edu/abstract_service.html">NASA Astrophysics Data System (ADS)</a></p> <p>Kittler, Fanny; Heimann, Martin; Kolle, Olaf; Zimov, Nikita; Zimov, Sergei; Göckede, Mathias</p> <p>2017-12-01</p> <p>Permafrost landscapes in northern high latitudes with their massive organic carbon stocks are an important, poorly known, component of the global carbon cycle. However, in light of future Arctic warming, the sustainability of these carbon pools is uncertain. To a large part, this is due to a limited understanding of the carbon cycle processes because of sparse observations in Arctic permafrost ecosystems. Here we present an eddy covariance data set covering more than 3 years of continuous CO2 and CH4 flux observations within a moist tussock tundra ecosystem near Chersky in north-eastern Siberia. Through parallel observations of a disturbed (drained) area and a control area nearby, we aim to evaluate the long-term effects of a persistently lowered water table on the net vertical carbon exchange budgets and the dominating biogeochemical mechanisms. Persistently drier soils trigger systematic shifts in the tundra ecosystem carbon cycle patterns. Both, uptake rates of CO2 and emissions of CH4 decreased. Year-round measurements emphasize the importance of the non-growing season—in particular the "zero-curtain" period in the fall—to the annual budget. Approximately 60% of the CO2 uptake in the growing season is lost during the cold seasons, while CH4 emissions during the non-growing season account for 30% of the annual budget. Year-to-year variability in temperature conditions during the late growing season was identified as the primary control of the interannual variability observed in the CO2 and CH4 fluxes.</p> </li> <li> <p><a target="_blank" rel="noopener noreferrer" onclick="trackOutboundLink('https://www.pubmedcentral.nih.gov/articlerender.fcgi?tool=pmcentrez&artid=5380966','PMC'); return false;" href="https://www.pubmedcentral.nih.gov/articlerender.fcgi?tool=pmcentrez&artid=5380966"><span>Rapid electron transfer by the carbon matrix in natural pyrogenic carbon</span></a></p> <p><a target="_blank" rel="noopener noreferrer" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?DB=pmc">PubMed Central</a></p> <p>Sun, Tianran; Levin, Barnaby D. A.; Guzman, Juan J. L.; Enders, Akio; Muller, David A.; Angenent, Largus T.; Lehmann, Johannes</p> <p>2017-01-01</p> <p>Surface functional groups constitute major electroactive components in pyrogenic carbon. However, the electrochemical properties of pyrogenic carbon matrices and the kinetic preference of functional groups or carbon matrices for electron transfer remain unknown. Here we show that environmentally relevant pyrogenic carbon with average H/C and O/C ratios of less than 0.35 and 0.09 can directly transfer electrons more than three times faster than the charging and discharging cycles of surface functional groups and have a 1.5 V potential range for biogeochemical reactions that invoke electron transfer processes. Surface functional groups contribute to the overall electron flux of pyrogenic carbon to a lesser extent with greater pyrolysis temperature due to lower charging and discharging capacities, although the charging and discharging kinetics remain unchanged. This study could spur the development of a new generation of biogeochemical electron flux models that focus on the bacteria–carbon–mineral conductive network. PMID:28361882</p> </li> <li> <p><a target="_blank" rel="noopener noreferrer" onclick="trackOutboundLink('http://adsabs.harvard.edu/abs/2017GMD....10.3481E','NASAADS'); return false;" href="http://adsabs.harvard.edu/abs/2017GMD....10.3481E"><span>An improved land biosphere module for use in the DCESS Earth system model (version 1.1) with application to the last glacial termination</span></a></p> <p><a target="_blank" rel="noopener noreferrer" href="http://adsabs.harvard.edu/abstract_service.html">NASA Astrophysics Data System (ADS)</a></p> <p>Eichinger, Roland; Shaffer, Gary; Albarrán, Nelson; Rojas, Maisa; Lambert, Fabrice</p> <p>2017-09-01</p> <p>Interactions between the land biosphere and the atmosphere play an important role for the Earth's carbon cycle and thus should be considered in studies of global carbon cycling and climate. Simple approaches are a useful first step in this direction but may not be applicable for certain climatic conditions. To improve the ability of the reduced-complexity Danish Center for Earth System Science (DCESS) Earth system model DCESS to address cold climate conditions, we reformulated the model's land biosphere module by extending it to include three dynamically varying vegetation zones as well as a permafrost component. The vegetation zones are formulated by emulating the behaviour of a complex land biosphere model. We show that with the new module, the size and timing of carbon exchanges between atmosphere and land are represented more realistically in cooling and warming experiments. In particular, we use the new module to address carbon cycling and climate change across the last glacial transition. Within the constraints provided by various proxy data records, we tune the DCESS model to a Last Glacial Maximum state and then conduct transient sensitivity experiments across the transition under the application of explicit transition functions for high-latitude ocean exchange, atmospheric dust, and the land ice sheet extent. We compare simulated time evolutions of global mean temperature, pCO2, atmospheric and oceanic carbon isotopes as well as ocean dissolved oxygen concentrations with proxy data records. In this way we estimate the importance of different processes across the transition with emphasis on the role of land biosphere variations and show that carbon outgassing from permafrost and uptake of carbon by the land biosphere broadly compensate for each other during the temperature rise of the early last deglaciation.</p> </li> <li> <p><a target="_blank" rel="noopener noreferrer" onclick="trackOutboundLink('https://www.osti.gov/biblio/947133-effects-harvest-management-practices-forest-biomass-soil-carbon-eucalypt-forests-new-south-wales-australia-simulations-forest-succession-model-linkages','SCIGOV-STC'); return false;" href="https://www.osti.gov/biblio/947133-effects-harvest-management-practices-forest-biomass-soil-carbon-eucalypt-forests-new-south-wales-australia-simulations-forest-succession-model-linkages"><span>Effects of harvest management practices on forest biomass and soil carbon in eucalypt forests in New South Wales, Australia: Simulations with the forest succession model LINKAGES</span></a></p> <p><a target="_blank" rel="noopener noreferrer" href="http://www.osti.gov/search">DOE Office of Scientific and Technical Information (OSTI.GOV)</a></p> <p>Ranatunga, Kemachandra; Keenan, Rodney J.; Wullschleger, Stan D</p> <p>2008-01-01</p> <p>Understanding long-term changes in forest ecosystem carbon stocks under forest management practices such as timber harvesting is important for assessing the contribution of forests to the global carbon cycle. Harvesting effects are complicated by the amount, type, and condition of residue left on-site, the decomposition rate of this residue, the incorporation of residue into soil organic matter and the rate of new detritus input to the forest floor from regrowing vegetation. In an attempt to address these complexities, the forest succession model LINKAGES was used to assess the production of aboveground biomass, detritus, and soil carbon stocks in native Eucalyptusmore » forests as influenced by five harvest management practices in New South Wales, Australia. The original decomposition sub-routines of LINKAGES were modified by adding components of the Rothamsted (RothC) soil organic matter turnover model. Simulation results using the new model were compared to data from long-term forest inventory plots. Good agreement was observed between simulated and measured above-ground biomass, but mixed results were obtained for basal area. Harvesting operations examined included removing trees for quota sawlogs (QSL, DBH >80 cm), integrated sawlogs (ISL, DBH >20 cm) and whole-tree harvesting in integrated sawlogs (WTH). We also examined the impact of different cutting cycles (20, 50 or 80 years) and intensities (removing 20, 50 or 80 m{sup 3}). Generally medium and high intensities of shorter cutting cycles in sawlog harvesting systems produced considerably higher soil carbon values compared to no harvesting. On average, soil carbon was 2-9% lower in whole-tree harvest simulations whereas in sawlog harvest simulations soil carbon was 5-17% higher than in no harvesting.« less</p> </li> <li> <p><a target="_blank" rel="noopener noreferrer" onclick="trackOutboundLink('https://www.ncbi.nlm.nih.gov/pubmed/26390852','PUBMED'); return false;" href="https://www.ncbi.nlm.nih.gov/pubmed/26390852"><span>Toward an integrated monitoring framework to assess the effects of tropical forest degradation and recovery on carbon stocks and biodiversity.</span></a></p> <p><a target="_blank" rel="noopener noreferrer" href="https://www.ncbi.nlm.nih.gov/entrez/query.fcgi?DB=pubmed">PubMed</a></p> <p>Bustamante, Mercedes M C; Roitman, Iris; Aide, T Mitchell; Alencar, Ane; Anderson, Liana O; Aragão, Luiz; Asner, Gregory P; Barlow, Jos; Berenguer, Erika; Chambers, Jeffrey; Costa, Marcos H; Fanin, Thierry; Ferreira, Laerte G; Ferreira, Joice; Keller, Michael; Magnusson, William E; Morales-Barquero, Lucia; Morton, Douglas; Ometto, Jean P H B; Palace, Michael; Peres, Carlos A; Silvério, Divino; Trumbore, Susan; Vieira, Ima C G</p> <p>2016-01-01</p> <p>Tropical forests harbor a significant portion of global biodiversity and are a critical component of the climate system. Reducing deforestation and forest degradation contributes to global climate-change mitigation efforts, yet emissions and removals from forest dynamics are still poorly quantified. We reviewed the main challenges to estimate changes in carbon stocks and biodiversity due to degradation and recovery of tropical forests, focusing on three main areas: (1) the combination of field surveys and remote sensing; (2) evaluation of biodiversity and carbon values under a unified strategy; and (3) research efforts needed to understand and quantify forest degradation and recovery. The improvement of models and estimates of changes of forest carbon can foster process-oriented monitoring of forest dynamics, including different variables and using spatially explicit algorithms that account for regional and local differences, such as variation in climate, soil, nutrient content, topography, biodiversity, disturbance history, recovery pathways, and socioeconomic factors. Generating the data for these models requires affordable large-scale remote-sensing tools associated with a robust network of field plots that can generate spatially explicit information on a range of variables through time. By combining ecosystem models, multiscale remote sensing, and networks of field plots, we will be able to evaluate forest degradation and recovery and their interactions with biodiversity and carbon cycling. Improving monitoring strategies will allow a better understanding of the role of forest dynamics in climate-change mitigation, adaptation, and carbon cycle feedbacks, thereby reducing uncertainties in models of the key processes in the carbon cycle, including their impacts on biodiversity, which are fundamental to support forest governance policies, such as Reducing Emissions from Deforestation and Forest Degradation. © 2015 John Wiley & Sons Ltd.</p> </li> <li> <p><a target="_blank" rel="noopener noreferrer" onclick="trackOutboundLink('http://adsabs.harvard.edu/abs/2018JPS...378..248L','NASAADS'); return false;" href="http://adsabs.harvard.edu/abs/2018JPS...378..248L"><span>Hierarchical NiCo-LDH@NiOOH core-shell heterostructure on carbon fiber cloth as battery-like electrode for supercapacitor</span></a></p> <p><a target="_blank" rel="noopener noreferrer" href="http://adsabs.harvard.edu/abstract_service.html">NASA Astrophysics Data System (ADS)</a></p> <p>Liang, Haoyan; Lin, Jinghuang; Jia, Henan; Chen, Shulin; Qi, Junlei; Cao, Jian; Lin, Tiesong; Fei, Weidong; Feng, Jicai</p> <p>2018-02-01</p> <p>Constructing rational structure and utilizing distinctive components are two important keys to promote the development of high performance supercapacitor. Herein, we adopt a facile two-step method to develop an in-situ heterostructure with NiCo-LDH nanowire as core and NiOOH nanosheets as shell on carbon fiber cloth. The resultant NiCo-LDH@NiOOH electrode exhibites a high specific capacitance of about 2622 F g-1 at 1 A g-1 and good cycling stability (88.5% remain after 10000 cycles). This reinforced electrochemical performance is benefit from the distinct core-shell structure, and takes advantage of the synergetic effect to supply more electrochemical active spots and pathways to accelerate electron and ion transport. Furthermore, the fabricated asymmetric supercapacitor of optimized NiCo-LDH@NiOOH//AC device displays a high energy density of 51.7 Wh kg-1 while the power density is 599 W kg-1 and presents a satisfying cycling performance.</p> </li> <li> <p><a target="_blank" rel="noopener noreferrer" onclick="trackOutboundLink('https://www.ncbi.nlm.nih.gov/pubmed/18522090','PUBMED'); return false;" href="https://www.ncbi.nlm.nih.gov/pubmed/18522090"><span>Life cycle assessment of greenhouse gas emissions from plug-in hybrid vehicles: implications for policy.</span></a></p> <p><a target="_blank" rel="noopener noreferrer" href="https://www.ncbi.nlm.nih.gov/entrez/query.fcgi?DB=pubmed">PubMed</a></p> <p>Samaras, Constantine; Meisterling, Kyle</p> <p>2008-05-01</p> <p>Plug-in hybrid electric vehicles (PHEVs), which use electricity from the grid to power a portion of travel, could play a role in reducing greenhouse gas (GHG) emissions from the transport sector. However, meaningful GHG emissions reductions with PHEVs are conditional on low-carbon electricity sources. We assess life cycle GHG emissions from PHEVs and find that they reduce GHG emissions by 32% compared to conventional vehicles, but have small reductions compared to traditional hybrids. Batteries are an important component of PHEVs, and GHGs associated with lithium-ion battery materials and production account for 2-5% of life cycle emissions from PHEVs. We consider cellulosic ethanol use and various carbon intensities of electricity. The reduced liquid fuel requirements of PHEVs could leverage limited cellulosic ethanol resources. Electricity generation infrastructure is long-lived, and technology decisions within the next decade about electricity supplies in the power sector will affectthe potential for large GHG emissions reductions with PHEVs for several decades.</p> </li> <li> <p><a target="_blank" rel="noopener noreferrer" onclick="trackOutboundLink('https://www.osti.gov/pages/biblio/1372400-electrolyte-volume-effects-electrochemical-performance-solid-electrolyte-interphase-si-graphite-nmc-lithium-ion-pouch-cells','SCIGOV-DOEP'); return false;" href="https://www.osti.gov/pages/biblio/1372400-electrolyte-volume-effects-electrochemical-performance-solid-electrolyte-interphase-si-graphite-nmc-lithium-ion-pouch-cells"><span>Electrolyte volume effects on electrochemical performance and solid electrolyte interphase in Si-graphite/NMC lithium-ion pouch cells</span></a></p> <p><a target="_blank" rel="noopener noreferrer" href="http://www.osti.gov/pages">DOE PAGES</a></p> <p>An, Seong Jin; Li, Jianlin; Daniel, Claus; ...</p> <p>2017-05-15</p> <p>This study aims to explore the correlations between electrolyte volume, electrochemical performance, and properties of the solid electrolyte interphase in pouch cells with Si-graphite composite anodes. The electrolyte is 1.2 M LiPF 6 in ethylene carbonate:ethylmethyl carbonate with 10 wt.% fluoroethylene carbonate. Single layer pouch cells (100 mAh) were constructed with 15 wt.% Si-graphite/LiNi 0.5Mn 0.3CO 0.2O 2 electrodes. It is found that a minimum electrolyte volume factor of 3.1 times the total pore volume of cell components (cathode, anode, and separator) is needed for better cycling stability. Less electrolyte causes increases in ohmic and charge transfer resistances. Lithium dendritesmore » are observed when the electrolyte volume factor is low. The resistances from the anodes become significant as the cells are discharged. As a result, solid electrolyte interphase thickness grows as the electrolyte volume factor increases and is non-uniform after cycling.« less</p> </li> <li> <p><a target="_blank" rel="noopener noreferrer" onclick="trackOutboundLink('http://adsabs.harvard.edu/abs/2015NatCC...5..459L','NASAADS'); return false;" href="http://adsabs.harvard.edu/abs/2015NatCC...5..459L"><span>Optimal stomatal behaviour around the world</span></a></p> <p><a target="_blank" rel="noopener noreferrer" href="http://adsabs.harvard.edu/abstract_service.html">NASA Astrophysics Data System (ADS)</a></p> <p>Lin, Yan-Shih; Medlyn, Belinda E.; Duursma, Remko A.; Prentice, I. Colin; Wang, Han; Baig, Sofia; Eamus, Derek; de Dios, Victor Resco; Mitchell, Patrick; Ellsworth, David S.; de Beeck, Maarten Op; Wallin, Göran; Uddling, Johan; Tarvainen, Lasse; Linderson, Maj-Lena; Cernusak, Lucas A.; Nippert, Jesse B.; Ocheltree, Troy W.; Tissue, David T.; Martin-Stpaul, Nicolas K.; Rogers, Alistair; Warren, Jeff M.; de Angelis, Paolo; Hikosaka, Kouki; Han, Qingmin; Onoda, Yusuke; Gimeno, Teresa E.; Barton, Craig V. M.; Bennie, Jonathan; Bonal, Damien; Bosc, Alexandre; Löw, Markus; Macinins-Ng, Cate; Rey, Ana; Rowland, Lucy; Setterfield, Samantha A.; Tausz-Posch, Sabine; Zaragoza-Castells, Joana; Broadmeadow, Mark S. J.; Drake, John E.; Freeman, Michael; Ghannoum, Oula; Hutley, Lindsay B.; Kelly, Jeff W.; Kikuzawa, Kihachiro; Kolari, Pasi; Koyama, Kohei; Limousin, Jean-Marc; Meir, Patrick; Lola da Costa, Antonio C.; Mikkelsen, Teis N.; Salinas, Norma; Sun, Wei; Wingate, Lisa</p> <p>2015-05-01</p> <p>Stomatal conductance (gs) is a key land-surface attribute as it links transpiration, the dominant component of global land evapotranspiration, and photosynthesis, the driving force of the global carbon cycle. Despite the pivotal role of gs in predictions of global water and carbon cycle changes, a global-scale database and an associated globally applicable model of gs that allow predictions of stomatal behaviour are lacking. Here, we present a database of globally distributed gs obtained in the field for a wide range of plant functional types (PFTs) and biomes. We find that stomatal behaviour differs among PFTs according to their marginal carbon cost of water use, as predicted by the theory underpinning the optimal stomatal model and the leaf and wood economics spectrum. We also demonstrate a global relationship with climate. These findings provide a robust theoretical framework for understanding and predicting the behaviour of gs across biomes and across PFTs that can be applied to regional, continental and global-scale modelling of ecosystem productivity, energy balance and ecohydrological processes in a future changing climate.</p> </li> <li> <p><a target="_blank" rel="noopener noreferrer" onclick="trackOutboundLink('http://adsabs.harvard.edu/abs/2017EGUGA..19.5882M','NASAADS'); return false;" href="http://adsabs.harvard.edu/abs/2017EGUGA..19.5882M"><span>Climate and the Carbon Cycle</span></a></p> <p><a target="_blank" rel="noopener noreferrer" href="http://adsabs.harvard.edu/abstract_service.html">NASA Astrophysics Data System (ADS)</a></p> <p>Manley, Jim</p> <p>2017-04-01</p> <p>Climate and the Carbon Cycle EOS3a Science in tomorrow's classroom Students, like too much of the American public, are largely unaware or apathetic to the changes in world climate and the impact that these changes have for life on Earth. A study conducted by Michigan State University and published in 2011 by Science Daily titled 'What carbon cycle? College students lack scientific literacy, study finds'. This study relates how 'most college students in the United States do not grasp the scientific basis of the carbon cycle - an essential skill in understanding the causes and consequences of climate change.' The study authors call for a new approach to teaching about climate. What if teachers better understood vital components of Earth's climate system and were able to impart his understanding to their students? What if students based their responses to the information taught not on emotion, but on a deeper understanding of the forces driving climate change, their analysis of the scientific evidence and in the context of earth system science? As a Middle School science teacher, I have been given the opportunity to use a new curriculum within TERC's EarthLabs collection, Climate and the Carbon Cycle, to awaken those brains and assist my students in making personal lifestyle choices based on what they had learned. In addition, with support from TERC and The University of Texas Institute for Geophysics I joined others to begin training other teachers on how to implement this curriculum in their classrooms to expose their students to our changing climate. Through my poster, I will give you (1) a glimpse into the challenges faced by today's science teachers in communicating the complicated, but ever-deepening understanding of the linkages between natural and human-driven factors on climate; (2) introduce you to a new module in the EarthLabs curriculum designed to expose teachers and students to global scientific climate data and instrumentation; and (3) illustrate how student worldviews are changed though exposure to the latest in scientific discovery and understanding.</p> </li> </ol> <div class="pull-right"> <ul class="pagination"> <li><a href="#" onclick='return showDiv("page_1");'>«</a></li> <li><a href="#" onclick='return showDiv("page_9");'>9</a></li> <li><a href="#" onclick='return showDiv("page_10");'>10</a></li> <li class="active"><span>11</span></li> <li><a href="#" onclick='return showDiv("page_12");'>12</a></li> <li><a href="#" onclick='return showDiv("page_13");'>13</a></li> <li><a href="#" onclick='return showDiv("page_25");'>»</a></li> </ul> </div> </div><!-- col-sm-12 --> </div><!-- row --> </div><!-- page_11 --> <div id="page_12" class="hiddenDiv"> <div class="row"> <div class="col-sm-12"> <div class="pull-right"> <ul class="pagination"> <li><a href="#" onclick='return showDiv("page_1");'>«</a></li> <li><a href="#" onclick='return showDiv("page_10");'>10</a></li> <li><a href="#" onclick='return showDiv("page_11");'>11</a></li> <li class="active"><span>12</span></li> <li><a href="#" onclick='return showDiv("page_13");'>13</a></li> <li><a href="#" onclick='return showDiv("page_14");'>14</a></li> <li><a href="#" onclick='return showDiv("page_25");'>»</a></li> </ul> </div> </div> </div> <div class="row"> <div class="col-sm-12"> <ol class="result-class" start="221"> <li> <p><a target="_blank" rel="noopener noreferrer" onclick="trackOutboundLink('http://adsabs.harvard.edu/abs/2016AGUFM.B21I0531H','NASAADS'); return false;" href="http://adsabs.harvard.edu/abs/2016AGUFM.B21I0531H"><span>Changes in Soil Carbon Storage in Industrial Forests of Western Oregon and Washington Following Modern Timber Harvesting Practices</span></a></p> <p><a target="_blank" rel="noopener noreferrer" href="http://adsabs.harvard.edu/abstract_service.html">NASA Astrophysics Data System (ADS)</a></p> <p>Holub, S. M.; Hatten, J. A.</p> <p>2016-12-01</p> <p>Carbon in forest soils is often overlooked because it is less conspicuous than the live trees, downed wood, and forest floor layer that are easily visible when walking through a forest. However, the amount of carbon in forest soils to one meter depth is generally one to two times the amount of carbon we see above ground in mature forests, making soils an important carbon storage pool in forest ecosystems. Given the large quantity of carbon stored in soil, there is some concern that disturbances to forest ecosystems could push some soils out of steady state and lead to a release of carbon from the soil, potentially contributing to the already large amount of greenhouse gas emissions from the burning of fossil fuels for energy. This has implications for the carbon neutrality of timberlands. Thus, careful investigation of the carbon cycle in forest soils is a key component in deciphering the gains and losses of carbon from forests, and ultimately understanding the effects of forest soils on the global carbon cycle. The study objective was to measure pre-harvest soil carbon stores to 1 m depth with enough precision to detect a small change upon resampling post-harvest. The 9 sites examined ranged from 100 to 400 Mg C / ha before harvest with minimum detectible differences around 5%. Three and a half years post-harvest the average of all 9 sites showed a very modest increase in mineral soil carbon as a result of modern timber harvest. Mineral soil carbon did not change significantly at 6 of the 9 sites, individually (range -2% to +5%), while two sites gained soil carbon (+6% and +11%) and soil carbon decreased at one site (-6%).</p> </li> <li> <p><a target="_blank" rel="noopener noreferrer" onclick="trackOutboundLink('https://www.ncbi.nlm.nih.gov/pubmed/22953777','PUBMED'); return false;" href="https://www.ncbi.nlm.nih.gov/pubmed/22953777"><span>Nanocarbon networks for advanced rechargeable lithium batteries.</span></a></p> <p><a target="_blank" rel="noopener noreferrer" href="https://www.ncbi.nlm.nih.gov/entrez/query.fcgi?DB=pubmed">PubMed</a></p> <p>Xin, Sen; Guo, Yu-Guo; Wan, Li-Jun</p> <p>2012-10-16</p> <p>Carbon is one of the essential elements in energy storage. In rechargeable lithium batteries, researchers have considered many types of nanostructured carbons, such as carbon nanoparticles, carbon nanotubes, graphene, and nanoporous carbon, as anode materials and, especially, as key components for building advanced composite electrode materials. Nanocarbons can form efficient three-dimensional conducting networks that improve the performance of electrode materials suffering from the limited kinetics of lithium storage. Although the porous structure guarantees a fast migration of Li ions, the nanocarbon network can serve as an effective matrix for dispersing the active materials to prevent them from agglomerating. The nanocarbon network also affords an efficient electron pathway to provide better electrical contacts. Because of their structural stability and flexibility, nanocarbon networks can alleviate the stress and volume changes that occur in active materials during the Li insertion/extraction process. Through the elegant design of hierarchical electrode materials with nanocarbon networks, researchers can improve both the kinetic performance and the structural stability of the electrode material, which leads to optimal battery capacity, cycling stability, and rate capability. This Account summarizes recent progress in the structural design, chemical synthesis, and characterization of the electrochemical properties of nanocarbon networks for Li-ion batteries. In such systems, storage occurs primarily in the non-carbon components, while carbon acts as the conductor and as the structural buffer. We emphasize representative nanocarbon networks including those that use carbon nanotubes and graphene. We discuss the role of carbon in enhancing the performance of various electrode materials in areas such as Li storage, Li ion and electron transport, and structural stability during cycling. We especially highlight the use of graphene to construct the carbon conducting network for alloy anodes, such as Si and Ge, to accelerate electron transport, alleviate volume change, and prevent the agglomeration of active nanoparticles. Finally, we describe the power of nanocarbon networks for the next generation rechargeable lithium batteries, including Li-S, Li-O(2), and Li-organic batteries, and provide insights into the design of ideal nanocarbon networks for these devices. In addition, we address the ways in which nanocarbon networks can expand the applications of rechargeable lithium batteries into the emerging fields of stationary energy storage and transportation.</p> </li> <li> <p><a target="_blank" rel="noopener noreferrer" onclick="trackOutboundLink('http://adsabs.harvard.edu/abs/2016JPS...307...17W','NASAADS'); return false;" href="http://adsabs.harvard.edu/abs/2016JPS...307...17W"><span>Conversion of uniform graphene oxide/polypyrrole composites into functionalized 3D carbon nanosheet frameworks with superior supercapacitive and sodium-ion storage properties</span></a></p> <p><a target="_blank" rel="noopener noreferrer" href="http://adsabs.harvard.edu/abstract_service.html">NASA Astrophysics Data System (ADS)</a></p> <p>Wang, Huanwen; Zhang, Yu; Sun, Wenping; Tan, Hui Teng; Franklin, Joseph B.; Guo, Yuanyuan; Fan, Haosen; Ulaganathan, Mani; Wu, Xing-Long; Luo, Zhong-Zhen; Madhavi, Srinivasan; Yan, Qingyu</p> <p>2016-03-01</p> <p>Two-dimensional (2D) graphene oxide/polypyrrole (GO/PPy) hybrid materials derived from in-situ polymerization are used as precursors for constructing functionalized three-dimensional (3D) porous nitrogen-doped carbon nanosheet frameworks (FT-PNCNFs) through a one-step activation strategy. In the formation process of FT-PNCNFs, PPY is directly converted into hierarchical porous nitrogen-doped carbon layers, while GO is simultaneously reduced to become electrically conductive. The complementary functions of individual components endow the FT-PNCNFs with excellent properties for both supercapacitors (SCs) and sodium ion batteries (SIBs) applications. When tested in symmetrical SC, the FT-PNCNFs demonstrate superior energy storage behaviour. At an extremely high scan rate of 3000 mV s-1, the cyclic voltammetry (CV) curve retains an inspiring quasi-rectangle shape in KOH solution. Meanwhile, high capacitances (∼247 F g-1 at 10 mV s-1; ∼146 F g-1 at 3000 mV s-1) and good cycling stability (∼95% retention after 8000 cycles) are achieved. In addition, an attractive SIB anode performance could be achieved. The FT-PNCNFs electrode delivers a reversible capacity of 187 mAh g-1 during 160th cycle at 100 mA g-1. Its reversible capacity retains 144 mAh g-1 after extending the number of cycles to 500 at 500 mA g-1.</p> </li> <li> <p><a target="_blank" rel="noopener noreferrer" onclick="trackOutboundLink('https://www.ncbi.nlm.nih.gov/pubmed/26765311','PUBMED'); return false;" href="https://www.ncbi.nlm.nih.gov/pubmed/26765311"><span>Root structure-function relationships in 74 species: evidence of a root economics spectrum related to carbon economy.</span></a></p> <p><a target="_blank" rel="noopener noreferrer" href="https://www.ncbi.nlm.nih.gov/entrez/query.fcgi?DB=pubmed">PubMed</a></p> <p>Roumet, Catherine; Birouste, Marine; Picon-Cochard, Catherine; Ghestem, Murielle; Osman, Normaniza; Vrignon-Brenas, Sylvain; Cao, Kun-Fang; Stokes, Alexia</p> <p>2016-05-01</p> <p>Although fine roots are important components of the global carbon cycle, there is limited understanding of root structure-function relationships among species. We determined whether root respiration rate and decomposability, two key processes driving carbon cycling but always studied separately, varied with root morphological and chemical traits, in a coordinated way that would demonstrate the existence of a root economics spectrum (RES). Twelve traits were measured on fine roots (diameter ≤ 2 mm) of 74 species (31 graminoids and 43 herbaceous and dwarf shrub eudicots) collected in three biomes. The findings of this study support the existence of a RES representing an axis of trait variation in which root respiration was positively correlated to nitrogen concentration and specific root length and negatively correlated to the root dry matter content, lignin : nitrogen ratio and the remaining mass after decomposition. This pattern of traits was highly consistent within graminoids but less consistent within eudicots, as a result of an uncoupling between decomposability and morphology, and of heterogeneity of individual roots of eudicots within the fine-root pool. The positive relationship found between root respiration and decomposability is essential for a better understanding of vegetation-soil feedbacks and for improving terrestrial biosphere models predicting the consequences of plant community changes for carbon cycling. © 2016 CNRS. New Phytologist © 2016 New Phytologist Trust.</p> </li> <li> <p><a target="_blank" rel="noopener noreferrer" onclick="trackOutboundLink('http://adsabs.harvard.edu/abs/2004PhDT.......227S','NASAADS'); return false;" href="http://adsabs.harvard.edu/abs/2004PhDT.......227S"><span>Studies of hexafluorophosphate, tetrafluoroborate, and perchlorate electro-intercalation into graphitic carbon</span></a></p> <p><a target="_blank" rel="noopener noreferrer" href="http://adsabs.harvard.edu/abstract_service.html">NASA Astrophysics Data System (ADS)</a></p> <p>Seel, Jennifer Ann</p> <p></p> <p>There has been some interest in using carbon materials as both working electrodes in electrochemical cells and rechargeable batteries [1--6]. This would result in the intercalation of not only of lithium ions into one carbon electrode but the anion component of the lithium salt, such as PF 6-, into the other carbon electrode. The intercalation of the anion component of the salt into carbon electrodes has not been studied extensively and it is not completely understood. The work presented here will expand on this rarely touched subject through electrochemical cycling as well as in-situ and ex-situ X-ray diffraction experiments. The anions that will be studied are: PF6- , BF4- and ClO4 -. It will be shown that anion intercalation occurs for various types of soft carbons and that the process can be greatly affected by the amount of turbostratic disorder present in the carbon material as well as by the specific anion used. It was discovered that using ethyl methyl sulfone, EMS, as the solvent component of the electrolyte resulted in more stable electrochemical cells than ethylene carbonate/diethyl carbonate, a more common solvent, at the high potentials required for anion intercalation. It was also discovered that PF 6 and BF4 formed staged phases during electrochemical cycling whereas ClO4 did not. The amount of disorder present in the carbon electrode did affect the intercalation of the anion. The samples with a greater amount of disorder present had a larger amount of capacity loss between charge and discharge capacities. It was also found that purer and more distinct staged phases occurred in the more ordered carbon samples. The turbostratically disordered carbon layers may rotate to accommodate PF6 and therefore become slightly more ordered. X-ray diffraction evidence suggests that intercalated PF6 molecules may be free-rotating between the carbon layers. However, the orientation of BF4 molecules between the carbon layers could not be determined. There may also be some co-intercalation of the solvent, mainly with ClO 4 and to a lesser extent BF4 and PF6. It is thought that a large amount of solvent co-intercalation occurs with ClO4 and this is the most probable reason why staged phases were not observed. An unfortunate aspect of this study is that dual carbon cells are not at all viable as commercial cells. The energy densities of dual carbon cells are much lower than the currently available lithium-ion cells. For dual carbon cells to become viable new inexpensive salts and solvents that can operate at high potentials and high concentrations must be discovered. With further investigation, combinations of different anions and solvents may result in higher specific capacities that would also make dual carbon cells more viable.</p> </li> <li> <p><a target="_blank" rel="noopener noreferrer" onclick="trackOutboundLink('http://adsabs.harvard.edu/abs/2017AGUFM.B51D1825R','NASAADS'); return false;" href="http://adsabs.harvard.edu/abs/2017AGUFM.B51D1825R"><span>Measuring soil organic matter turn over and carbon stabilisation in pasture soils using 13C enrichment methodology.</span></a></p> <p><a target="_blank" rel="noopener noreferrer" href="http://adsabs.harvard.edu/abstract_service.html">NASA Astrophysics Data System (ADS)</a></p> <p>Robinson, J. M.; Barker, S.; Schipper, L. A.</p> <p>2017-12-01</p> <p>Carbon storage in soil is a balance between photosynthesis and respiration, however, not all C compounds decompose equally in soil. Soil C consists of several fractions of C ranging from, accessible C (rapidly cycling) to stored or protected C (slow cycling). The key to increasing C storage is through the transfer of soil C from this accessible fraction, where it can be easily lost through microbial degradation, into the more stable fraction. With the increasing use of isotope enrichment techniques, 13C may be used to trace the movement of newly incorporated carbon in soil and examine how land management practises affect carbon storage. A laboratory method was developed to rapidly analyse soil respired CO2 for δ13C to determine the temperature sensitivity of newly incorporated 13C enriched carbon. A Horotiu silt loam (2 mm sieved, 60% MWHC) was mixed with 13C enriched ryegrass/clover plant matter in Hungate tubes and incubated for 5 hours at 20 temperatures( 4 - 50 °C) using a temperature gradient method (Robinson J. M., et al, (2017) Biogeochemistry, 13, 101-112). The respired CO2 was analysed using a modified Los Gatos, Off-axis ICOS carbon dioxide analyser. This method was able to analyse the δ13C signature of respired CO2 as long as a minimum concentration of CO2 was produced per tube. Further analysis used a two-component mixing model to separate the CO2 into source components to determine the contribution of added C and soil to total respiration. Preliminary data showed the decomposition of the two sources of C were both temperature dependant. Overall this method is a relatively quick and easy way to analyse δ13C of respired soil CO2 samples, and will allow for the testing of the effects of multiple variables on the decomposition of carbon fractions in future use.</p> </li> <li> <p><a target="_blank" rel="noopener noreferrer" onclick="trackOutboundLink('http://adsabs.harvard.edu/abs/2009EOSTr..90..102M','NASAADS'); return false;" href="http://adsabs.harvard.edu/abs/2009EOSTr..90..102M"><span>A U.S. Carbon Cycle Science Plan</span></a></p> <p><a target="_blank" rel="noopener noreferrer" href="http://adsabs.harvard.edu/abstract_service.html">NASA Astrophysics Data System (ADS)</a></p> <p>Michalak, Anna M.; Jackson, Rob; Marland, Gregg; Sabine, Christopher</p> <p>2009-03-01</p> <p>First Meeting of the Carbon Cycle Science Working Group; Washington, D. C., 17-18 November 2008; The report “A U.S. carbon cycle science plan” (J. L. Sarmiento and S. C. Wofsy, U.S. Global Change Res. Program, Washington, D. C., 1999) outlined research priorities and promoted coordinated carbon cycle research across federal agencies for nearly a decade. Building on this framework and subsequent reports (available at http://www.carboncyclescience.gov/docs.php), the Carbon Cycle Science Working Group (CCSWG) was formed in 2008 to develop an updated strategy for the next decade. The recommendations of the CCSWG will go to agency managers who have collective responsibility for setting national carbon cycle science priorities and for sponsoring much of the carbon cycle research in the United States.</p> </li> <li> <p><a target="_blank" rel="noopener noreferrer" onclick="trackOutboundLink('https://www.fs.usda.gov/treesearch/pubs/26825','TREESEARCH'); return false;" href="https://www.fs.usda.gov/treesearch/pubs/26825"><span>Wood CO2 efflux in a primary tropical rain forest</span></a></p> <p><a target="_blank" rel="noopener noreferrer" href="http://www.fs.usda.gov/treesearch/">Treesearch</a></p> <p>Molly A. Cavaleri; Steven F. Oberbauer; Michael G. Ryan</p> <p>2006-01-01</p> <p>The balance between photosynthesis and plant respiration in tropical forests may substantially affect the global carbon cycle. Woody tissue CO2 efflux is a major component of total plant respiration, but estimates of ecosystem-scale rates are uncertain because of poor sampling in the upper canopy and across landscapes. To overcome these problems, we used a portable...</p> </li> <li> <p><a target="_blank" rel="noopener noreferrer" onclick="trackOutboundLink('https://www.ncbi.nlm.nih.gov/pubmed/18200846','PUBMED'); return false;" href="https://www.ncbi.nlm.nih.gov/pubmed/18200846"><span>Major structural components in freshwater dissolved organic matter.</span></a></p> <p><a target="_blank" rel="noopener noreferrer" href="https://www.ncbi.nlm.nih.gov/entrez/query.fcgi?DB=pubmed">PubMed</a></p> <p>Lam, Buuan; Baer, Andrew; Alaee, Mehran; Lefebvre, Brent; Moser, Arvin; Williams, Antony; Simpson, André J</p> <p>2007-12-15</p> <p>Dissolved organic matter (DOM) contains a complex array of chemical components that are intimately linked to many environmental processes, including the global carbon cycle, and the fate and transport of chemical pollutants. Despite its importance, fundamental aspects, such as the structural components in DOM remain elusive, due in part to the molecular complexity of the material. Here, we utilize multidimensional nuclear magnetic resonance spectroscopy to demonstrate the major structural components in Lake Ontario DOM. These include carboxyl-rich alicyclic molecules (CRAM), heteropolysaccharides, and aromatic compounds, which are consistent with components recently identified in marine dissolved organic matter. In addition, long-range proton-carbon correlations are obtained for DOM, which support the existence of material derived from linear terpenoids (MDLT). It is tentatively suggested that the bulk of freshwater dissolved organic matter is aliphatic in nature, with CRAM derived from cyclic terpenoids, and MDLT derived from linear terpenoids. This is in agreement with previous reports which indicate terpenoids as major precursors of DOM. At this time it is not clear in Lake Ontario whether these precursors are of terrestrial or aquatic origin or whether transformations proceed via biological and/ or photochemical processes.</p> </li> <li> <p><a target="_blank" rel="noopener noreferrer" onclick="trackOutboundLink('https://www.ncbi.nlm.nih.gov/pubmed/27335019','PUBMED'); return false;" href="https://www.ncbi.nlm.nih.gov/pubmed/27335019"><span>The influence of biomass energy consumption on CO2 emissions: a wavelet coherence approach.</span></a></p> <p><a target="_blank" rel="noopener noreferrer" href="https://www.ncbi.nlm.nih.gov/entrez/query.fcgi?DB=pubmed">PubMed</a></p> <p>Bilgili, Faik; Öztürk, İlhan; Koçak, Emrah; Bulut, Ümit; Pamuk, Yalçın; Muğaloğlu, Erhan; Bağlıtaş, Hayriye H</p> <p>2016-10-01</p> <p>In terms of today, one may argue, throughout observations from energy literature papers, that (i) one of the main contributors of the global warming is carbon dioxide emissions, (ii) the fossil fuel energy usage greatly contributes to the carbon dioxide emissions, and (iii) the simulations from energy models attract the attention of policy makers to renewable energy as alternative energy source to mitigate the carbon dioxide emissions. Although there appears to be intensive renewable energy works in the related literature regarding renewables' efficiency/impact on environmental quality, a researcher might still need to follow further studies to review the significance of renewables in the environment since (i) the existing seminal papers employ time series models and/or panel data models or some other statistical observation to detect the role of renewables in the environment and (ii) existing papers consider mostly aggregated renewable energy source rather than examining the major component(s) of aggregated renewables. This paper attempted to examine clearly the impact of biomass on carbon dioxide emissions in detail through time series and frequency analyses. Hence, the paper follows wavelet coherence analyses. The data covers the US monthly observations ranging from 1984:1 to 2015 for the variables of total energy carbon dioxide emissions, biomass energy consumption, coal consumption, petroleum consumption, and natural gas consumption. The paper thus, throughout wavelet coherence and wavelet partial coherence analyses, observes frequency properties as well as time series properties of relevant variables to reveal the possible significant influence of biomass usage on the emissions in the USA in both the short-term and the long-term cycles. The paper also reveals, finally, that the biomass consumption mitigates CO2 emissions in the long run cycles after the year 2005 in the USA.</p> </li> <li> <p><a target="_blank" rel="noopener noreferrer" onclick="trackOutboundLink('https://pubs.er.usgs.gov/publication/70182175','USGSPUBS'); return false;" href="https://pubs.er.usgs.gov/publication/70182175"><span>CO2 and CH4 emissions from streams in a lake-rich landscape: Patterns, controls, and regional significance</span></a></p> <p><a target="_blank" rel="noopener noreferrer" href="http://pubs.er.usgs.gov/pubs/index.jsp?view=adv">USGS Publications Warehouse</a></p> <p>Crawford, John T.; Lottig, Noah R.; Stanley, Emily H.; Walker, John F.; Hanson, Paul C.; Finlay, Jacques C.; Striegl, Robert G.</p> <p>2014-01-01</p> <p>Aquatic ecosystems are important components of landscape carbon budgets. In lake-rich landscapes, both lakes and streams may be important sources of carbon gases (CO2 and CH4) to the atmosphere, but the processes that control gas concentrations and emissions in these interconnected landscapes have not been adequately addressed. We use multiple data sets that vary in their spatial and temporal extent during 2001–2012 to investigate the carbon gas source strength of streams in a lake-rich landscape and to determine the contribution of lakes, metabolism, and groundwater to stream CO2 and CH4. We show that streams emit roughly the same mass of CO2 (23.4 Gg C yr−1; 0.49 mol CO2 m−2 d−1) as lakes at a regional scale (27 Gg C yr−1) and that stream CH4 emissions (189 Mg C yr−1; 8.46 mmol CH4 m−2 d−1) are an important component of the regional greenhouse gas balance. Gas transfer velocity variability (range = 0.34 to 13.5 m d−1) contributed to the variability of gas flux in this landscape. Groundwater inputs and in-stream metabolism control stream gas supersaturation at the landscape scale, while carbon cycling in lakes and deep groundwaters does not control downstream gas emissions. Our results indicate the need to consider connectivity of all aquatic ecosystems (lakes, streams, wetlands, and groundwater) in lake-rich landscapes and their connections with the terrestrial environment in order to understand the full nature of the carbon cycle.</p> </li> <li> <p><a target="_blank" rel="noopener noreferrer" onclick="trackOutboundLink('https://pubs.er.usgs.gov/publication/70146739','USGSPUBS'); return false;" href="https://pubs.er.usgs.gov/publication/70146739"><span>Carbon stocks of trees killed by bark beetles and wildfire in the western United States</span></a></p> <p><a target="_blank" rel="noopener noreferrer" href="http://pubs.er.usgs.gov/pubs/index.jsp?view=adv">USGS Publications Warehouse</a></p> <p>Hicke, Jeffrey A.; Meddens, Arjan J.H.; Allen, Craig D.; Kolden, Crystal A.</p> <p>2013-01-01</p> <p>Forests are major components of the carbon cycle, and disturbances are important influences of forest carbon. Our objective was to contribute to the understanding of forest carbon cycling by quantifying the amount of carbon in trees killed by two disturbance types, fires and bark beetles, in the western United States in recent decades. We combined existing spatial data sets of forest biomass, burn severity, and beetle-caused tree mortality to estimate the amount of aboveground and belowground carbon in killed trees across the region. We found that during 1984-2010, fires killed trees that contained 5-11 Tg C year-1 and during 1997-2010, beetles killed trees that contained 2-24 Tg C year-1, with more trees killed since 2000 than in earlier periods. Over their periods of record, amounts of carbon in trees killed by fires and by beetle outbreaks were similar, and together these disturbances killed trees representing 9% of the total tree carbon in western forests, a similar amount to harvesting. Fires killed more trees in lower-elevation forest types such as Douglas-fir than higher-elevation forest types, whereas bark beetle outbreaks also killed trees in higher-elevation forest types such as lodgepole pine and Engelmann spruce. Over 15% of the carbon in lodgepole pine and spruce/fir forest types was in trees killed by beetle outbreaks; other forest types had 5-10% of the carbon in killed trees. Our results document the importance of these natural disturbances in the carbon budget of the western United States.</p> </li> <li> <p><a target="_blank" rel="noopener noreferrer" onclick="trackOutboundLink('https://www.osti.gov/servlets/purl/1372999','SCIGOV-STC'); return false;" href="https://www.osti.gov/servlets/purl/1372999"><span></span></a></p> <p><a target="_blank" rel="noopener noreferrer" href="http://www.osti.gov/search">DOE Office of Scientific and Technical Information (OSTI.GOV)</a></p> <p>Yang, Qichun; Zhang, Xuesong; Xu, Xingya</p> <p></p> <p>Riverine carbon cycling is an important, but insufficiently investigated component of the global carbon cycle. Analyses of environmental controls on riverine carbon cycling are critical for improved understanding of mechanisms regulating carbon processing and storage along the terrestrial-aquatic continuum. Here, we compile and analyze riverine dissolved organic carbon (DOC) concentration data from 1402 United States Geological Survey (USGS) gauge stations to examine the spatial variability and environmental controls of DOC concentrations in the United States (U.S.) surface waters. DOC concentrations exhibit high spatial variability, with an average of 6.42 ± 6.47 mg C/ L (Mean ± Standard Deviation). In general,more » high DOC concentrations occur in the Upper Mississippi River basin and the Southeastern U.S., while low concentrations are mainly distributed in the Western U.S. Single-factor analysis indicates that slope of drainage areas, wetlands, forests, percentage of first-order streams, and instream nutrients (such as nitrogen and phosphorus) pronouncedly influence DOC concentrations, but the explanatory power of each bivariate model is lower than 35%. Analyses based on the general multi-linear regression models suggest DOC concentrations are jointly impacted by multiple factors. Soil properties mainly show positive correlations with DOC concentrations; forest and shrub lands have positive correlations with DOC concentrations, but urban area and croplands demonstrate negative impacts; total instream phosphorus and dam density correlate positively with DOC concentrations. Notably, the relative importance of these environmental controls varies substantially across major U.S. water resource regions. In addition, DOC concentrations and environmental controls also show significant variability from small streams to large rivers, which may be caused by changing carbon sources and removal rates by river orders. In sum, our results reveal that general multi-linear regression analysis of twenty one terrestrial and aquatic environmental factors can partially explain (56%) the DOC concentration variation. In conclusion, this study highlights the complexity of the interactions among these environmental factors in determining DOC concentrations, thus calls for processes-based, non-linear methodologies to constrain uncertainties in riverine DOC cycling.« less</p> </li> <li> <p><a target="_blank" rel="noopener noreferrer" onclick="trackOutboundLink('http://adsabs.harvard.edu/abs/2007AGUFMED23A0962O','NASAADS'); return false;" href="http://adsabs.harvard.edu/abs/2007AGUFMED23A0962O"><span>The GLOBE Carbon Project: Integrating the Science of Carbon Cycling and Climate Change into K-12 Classrooms.</span></a></p> <p><a target="_blank" rel="noopener noreferrer" href="http://adsabs.harvard.edu/abstract_service.html">NASA Astrophysics Data System (ADS)</a></p> <p>Ollinger, S. V.; Silverberg, S.; Albrechtova, J.; Freuder, R.; Gengarelly, L.; Martin, M.; Randolph, G.; Schloss, A.</p> <p>2007-12-01</p> <p>The global carbon cycle is a key regulator of the Earth's climate and is central to the normal function of ecological systems. Because rising atmospheric CO2 is the principal cause of climate change, understanding how ecosystems cycle and store carbon has become an extremely important issue. In recent years, the growing importance of the carbon cycle has brought it to the forefront of both science and environmental policy. The need for better scientific understanding has led to establishment of numerous research programs, such as the North American Carbon Program (NACP), which seeks to understand controls on carbon cycling under present and future conditions. Parallel efforts are greatly needed to integrate state-of-the-art science on the carbon cycle and its importance to climate with education and outreach efforts that help prepare society to make sound decisions on energy use, carbon management and climate change adaptation. Here, we present a new effort that joins carbon cycle scientists with the International GLOBE Education program to develop carbon cycle activities for K-12 classrooms. The GLOBE Carbon Cycle project is focused on bringing cutting edge research and research techniques in the field of terrestrial ecosystem carbon cycling into the classroom. Students will collect data about their school field site through existing protocols of phenology, land cover and soils as well as new protocols focused on leaf traits, and ecosystem growth and change. They will also participate in classroom activities to understand carbon cycling in terrestrial ecosystems, these will include plant- a-plant experiments, hands-on demonstrations of various concepts, and analysis of collected data. In addition to the traditional GLOBE experience, students will have the opportunity to integrate their data with emerging and expanding technologies including global and local carbon cycle models and remote sensing toolkits. This program design will allow students to explore research questions from local to global scales with both present and future environmental conditions.</p> </li> <li> <p><a target="_blank" rel="noopener noreferrer" onclick="trackOutboundLink('https://ntrs.nasa.gov/search.jsp?R=20040068271&hterms=productivity&qs=Ntx%3Dmode%2Bmatchall%26Ntk%3DAll%26N%3D0%26No%3D30%26Ntt%3Dproductivity','NASA-TRS'); return false;" href="https://ntrs.nasa.gov/search.jsp?R=20040068271&hterms=productivity&qs=Ntx%3Dmode%2Bmatchall%26Ntk%3DAll%26N%3D0%26No%3D30%26Ntt%3Dproductivity"><span>PhyLM: A Mission Design Concept for an Optical/Lidar Instrument to Measure Ocean Productivity and Aerosols from Space</span></a></p> <p><a target="_blank" rel="noopener noreferrer" href="http://ntrs.nasa.gov/search.jsp">NASA Technical Reports Server (NTRS)</a></p> <p>Gervin, Janette C.; Behrenfeld, Michael; McClain, Charles R.; Spinhirne, James; Purves, Lloyd; Wood, H. John; Roberto, Michael R.</p> <p>2004-01-01</p> <p>The Physiology Lidar-Multispectral Mission (PhyLM) is intended to explore the complex ecosystems of our global oceans. New "inversion" methods and improved understanding of marine optics have opened the door to quantifying a range of critical ocean properties. This new information could revolutionize our understanding of global ocean processes, such as phytoplankton growth, harmful algal blooms, carbon fluxes between major pools and the productivity equation. The new science requires new measurements not addressed by currently planned space missions. PhyLM will combine active and advanced passive remote sensing technologies to quantify standing stocks and fluxes of climate-critical components of the Ocean carbon cycle to meet these science providing multispectral bands from the far UV through the near infrared (340 - 1250 nm) at a ground resolution of 250 m. Improved detectors, filters, mirrors, digitization and focal plane design will offer an overall higher-quality data product. The unprecedented accuracy and precision of the absolute water-leaving radiances will support inversion- based quantification of an expanded set of ocean carbon cycle components. The dual- wavelength (532 & 1064 nm) Nd:Yag Lidar will enhance the accuracy and precision of the passive data by providing aerosol profiles for atmospheric correction and coincident active measurements of backscattering. The Lidar will also examine dark-side fluorescence as an additional approach to quantifying phytoplankton biomass in highly productive regions.</p> </li> <li> <p><a target="_blank" rel="noopener noreferrer" onclick="trackOutboundLink('https://www.ncbi.nlm.nih.gov/pubmed/19265020','PUBMED'); return false;" href="https://www.ncbi.nlm.nih.gov/pubmed/19265020"><span>Drought sensitivity of the Amazon rainforest.</span></a></p> <p><a target="_blank" rel="noopener noreferrer" href="https://www.ncbi.nlm.nih.gov/entrez/query.fcgi?DB=pubmed">PubMed</a></p> <p>Phillips, Oliver L; Aragão, Luiz E O C; Lewis, Simon L; Fisher, Joshua B; Lloyd, Jon; López-González, Gabriela; Malhi, Yadvinder; Monteagudo, Abel; Peacock, Julie; Quesada, Carlos A; van der Heijden, Geertje; Almeida, Samuel; Amaral, Iêda; Arroyo, Luzmila; Aymard, Gerardo; Baker, Tim R; Bánki, Olaf; Blanc, Lilian; Bonal, Damien; Brando, Paulo; Chave, Jerome; de Oliveira, Atila Cristina Alves; Cardozo, Nallaret Dávila; Czimczik, Claudia I; Feldpausch, Ted R; Freitas, Maria Aparecida; Gloor, Emanuel; Higuchi, Niro; Jiménez, Eliana; Lloyd, Gareth; Meir, Patrick; Mendoza, Casimiro; Morel, Alexandra; Neill, David A; Nepstad, Daniel; Patiño, Sandra; Peñuela, Maria Cristina; Prieto, Adriana; Ramírez, Fredy; Schwarz, Michael; Silva, Javier; Silveira, Marcos; Thomas, Anne Sota; Steege, Hans Ter; Stropp, Juliana; Vásquez, Rodolfo; Zelazowski, Przemyslaw; Alvarez Dávila, Esteban; Andelman, Sandy; Andrade, Ana; Chao, Kuo-Jung; Erwin, Terry; Di Fiore, Anthony; Honorio C, Eurídice; Keeling, Helen; Killeen, Tim J; Laurance, William F; Peña Cruz, Antonio; Pitman, Nigel C A; Núñez Vargas, Percy; Ramírez-Angulo, Hirma; Rudas, Agustín; Salamão, Rafael; Silva, Natalino; Terborgh, John; Torres-Lezama, Armando</p> <p>2009-03-06</p> <p>Amazon forests are a key but poorly understood component of the global carbon cycle. If, as anticipated, they dry this century, they might accelerate climate change through carbon losses and changed surface energy balances. We used records from multiple long-term monitoring plots across Amazonia to assess forest responses to the intense 2005 drought, a possible analog of future events. Affected forest lost biomass, reversing a large long-term carbon sink, with the greatest impacts observed where the dry season was unusually intense. Relative to pre-2005 conditions, forest subjected to a 100-millimeter increase in water deficit lost 5.3 megagrams of aboveground biomass of carbon per hectare. The drought had a total biomass carbon impact of 1.2 to 1.6 petagrams (1.2 x 10(15) to 1.6 x 10(15) grams). Amazon forests therefore appear vulnerable to increasing moisture stress, with the potential for large carbon losses to exert feedback on climate change.</p> </li> <li> <p><a target="_blank" rel="noopener noreferrer" onclick="trackOutboundLink('http://adsabs.harvard.edu/abs/2015JPS...295..190X','NASAADS'); return false;" href="http://adsabs.harvard.edu/abs/2015JPS...295..190X"><span>Sulfone-carbonate ternary electrolyte with further increased capacity retention and burn resistance for high voltage lithium ion batteries</span></a></p> <p><a target="_blank" rel="noopener noreferrer" href="http://adsabs.harvard.edu/abstract_service.html">NASA Astrophysics Data System (ADS)</a></p> <p>Xue, Leigang; Lee, Seung-Yul; Zhao, Zuofeng; Angell, C. Austen</p> <p>2015-11-01</p> <p>Safety and high energy density are the two focus issues for current lithium ion batteries. For safety, it has been demonstrated that sulfone electrolytes are much less flammable than the prevailing all-carbonate type, and they are also promising for high voltage batteries due to the high oxidization resistance. However, the high melting points and viscosities greatly restricted their application. Based on our previous work on use of fluidity-enhancing cosolvents to make binary sulfone-carbonate electrolytes, we report here a three-component system that is more conductive and should be even less flammable while additionally having better low temperature stability. The conductivity-viscosity relations have been determined for this electrolyte and are comparable to those of the "standard" carbonate electrolyte. The additional component also produces much improved capacity retention for the LiNi0.5Mn1.5O4 cathode. As with carbonate electrolytes, increase of temperature to 55 °C leads to rapid capacity decrease during cycling, but the capacity loss is due to the salt, not the solvent. The high discharge capacity observed at 25 °C when LiBF4 replaces LiPF6, is fully retained at 55 °C.</p> </li> <li> <p><a target="_blank" rel="noopener noreferrer" onclick="trackOutboundLink('http://adsabs.harvard.edu/abs/2016ESD.....7..649R','NASAADS'); return false;" href="http://adsabs.harvard.edu/abs/2016ESD.....7..649R"><span>Divergent predictions of carbon storage between two global land models: attribution of the causes through traceability analysis</span></a></p> <p><a target="_blank" rel="noopener noreferrer" href="http://adsabs.harvard.edu/abstract_service.html">NASA Astrophysics Data System (ADS)</a></p> <p>Rafique, Rashid; Xia, Jianyang; Hararuk, Oleksandra; Asrar, Ghassem R.; Leng, Guoyong; Wang, Yingping; Luo, Yiqi</p> <p>2016-07-01</p> <p>Representations of the terrestrial carbon cycle in land models are becoming increasingly complex. It is crucial to develop approaches for critical assessment of the complex model properties in order to understand key factors contributing to models' performance. In this study, we applied a traceability analysis which decomposes carbon cycle models into traceable components, for two global land models (CABLE and CLM-CASA') to diagnose the causes of their differences in simulating ecosystem carbon storage capacity. Driven with similar forcing data, CLM-CASA' predicted ˜ 31 % larger carbon storage capacity than CABLE. Since ecosystem carbon storage capacity is a product of net primary productivity (NPP) and ecosystem residence time (τE), the predicted difference in the storage capacity between the two models results from differences in either NPP or τE or both. Our analysis showed that CLM-CASA' simulated 37 % higher NPP than CABLE. On the other hand, τE, which was a function of the baseline carbon residence time (τ'E) and environmental effect on carbon residence time, was on average 11 years longer in CABLE than CLM-CASA'. This difference in τE was mainly caused by longer τ'E of woody biomass (23 vs. 14 years in CLM-CASA'), and higher proportion of NPP allocated to woody biomass (23 vs. 16 %). Differences in environmental effects on carbon residence times had smaller influences on differences in ecosystem carbon storage capacities compared to differences in NPP and τ'E. Overall, the traceability analysis showed that the major causes of different carbon storage estimations were found to be parameters setting related to carbon input and baseline carbon residence times between two models.</p> </li> <li> <p><a target="_blank" rel="noopener noreferrer" onclick="trackOutboundLink('https://www.osti.gov/pages/biblio/1256395-divergent-predictions-carbon-storage-between-two-global-land-models-attribution-causes-through-traceability-analysis','SCIGOV-DOEP'); return false;" href="https://www.osti.gov/pages/biblio/1256395-divergent-predictions-carbon-storage-between-two-global-land-models-attribution-causes-through-traceability-analysis"><span>Divergent predictions of carbon storage between two global land models: Attribution of the causes through traceability analysis</span></a></p> <p><a target="_blank" rel="noopener noreferrer" href="http://www.osti.gov/pages">DOE PAGES</a></p> <p>Rafique, Rashid; Xia, Jianyang; Hararuk, Oleksandra; ...</p> <p>2016-07-29</p> <p>Representations of the terrestrial carbon cycle in land models are becoming increasingly complex. It is crucial to develop approaches for critical assessment of the complex model properties in order to understand key factors contributing to models' performance. In this study, we applied a traceability analysis which decomposes carbon cycle models into traceable components, for two global land models (CABLE and CLM-CASA') to diagnose the causes of their differences in simulating ecosystem carbon storage capacity. Driven with similar forcing data, CLM-CASA' predicted – 31 % larger carbon storage capacity than CABLE. Since ecosystem carbon storage capacity is a product of net primary productivitymore » (NPP) and ecosystem residence time ( τ E), the predicted difference in the storage capacity between the two models results from differences in either NPP or τ E or both. Our analysis showed that CLM-CASA'simulated 37 % higher NPP than CABLE. On the other hand, τ E, which was a function of the baseline carbon residence time ( τ' E) and environmental effect on carbon residence time, was on average 11 years longer in CABLE than CLM-CASA'. This difference in τ E was mainly caused by longer τ' E of woody biomass (23 vs. 14 years in CLM-CASA'), and higher proportion of NPP allocated to woody biomass (23 vs. 16 %). Differences in environmental effects on carbon residence times had smaller influences on differences in ecosystem carbon storage capacities compared to differences in NPP and τ' E. Altogether, the traceability analysis showed that the major causes of different carbon storage estimations were found to be parameters setting related to carbon input and baseline carbon residence times between two models.« less</p> </li> <li> <p><a target="_blank" rel="noopener noreferrer" onclick="trackOutboundLink('https://www.osti.gov/servlets/purl/1256395','SCIGOV-STC'); return false;" href="https://www.osti.gov/servlets/purl/1256395"><span>Divergent predictions of carbon storage between two global land models: Attribution of the causes through traceability analysis</span></a></p> <p><a target="_blank" rel="noopener noreferrer" href="http://www.osti.gov/search">DOE Office of Scientific and Technical Information (OSTI.GOV)</a></p> <p>Rafique, Rashid; Xia, Jianyang; Hararuk, Oleksandra</p> <p></p> <p>Representations of the terrestrial carbon cycle in land models are becoming increasingly complex. It is crucial to develop approaches for critical assessment of the complex model properties in order to understand key factors contributing to models' performance. In this study, we applied a traceability analysis which decomposes carbon cycle models into traceable components, for two global land models (CABLE and CLM-CASA') to diagnose the causes of their differences in simulating ecosystem carbon storage capacity. Driven with similar forcing data, CLM-CASA' predicted – 31 % larger carbon storage capacity than CABLE. Since ecosystem carbon storage capacity is a product of net primary productivitymore » (NPP) and ecosystem residence time ( τ E), the predicted difference in the storage capacity between the two models results from differences in either NPP or τ E or both. Our analysis showed that CLM-CASA'simulated 37 % higher NPP than CABLE. On the other hand, τ E, which was a function of the baseline carbon residence time ( τ' E) and environmental effect on carbon residence time, was on average 11 years longer in CABLE than CLM-CASA'. This difference in τ E was mainly caused by longer τ' E of woody biomass (23 vs. 14 years in CLM-CASA'), and higher proportion of NPP allocated to woody biomass (23 vs. 16 %). Differences in environmental effects on carbon residence times had smaller influences on differences in ecosystem carbon storage capacities compared to differences in NPP and τ' E. Altogether, the traceability analysis showed that the major causes of different carbon storage estimations were found to be parameters setting related to carbon input and baseline carbon residence times between two models.« less</p> </li> </ol> <div class="pull-right"> <ul class="pagination"> <li><a href="#" onclick='return showDiv("page_1");'>«</a></li> <li><a href="#" onclick='return showDiv("page_10");'>10</a></li> <li><a href="#" onclick='return showDiv("page_11");'>11</a></li> <li class="active"><span>12</span></li> <li><a href="#" onclick='return showDiv("page_13");'>13</a></li> <li><a href="#" onclick='return showDiv("page_14");'>14</a></li> <li><a href="#" onclick='return showDiv("page_25");'>»</a></li> </ul> </div> </div><!-- col-sm-12 --> </div><!-- row --> </div><!-- page_12 --> <div id="page_13" class="hiddenDiv"> <div class="row"> <div class="col-sm-12"> <div class="pull-right"> <ul class="pagination"> <li><a href="#" onclick='return showDiv("page_1");'>«</a></li> <li><a href="#" onclick='return showDiv("page_11");'>11</a></li> <li><a href="#" onclick='return showDiv("page_12");'>12</a></li> <li class="active"><span>13</span></li> <li><a href="#" onclick='return showDiv("page_14");'>14</a></li> <li><a href="#" onclick='return showDiv("page_15");'>15</a></li> <li><a href="#" onclick='return showDiv("page_25");'>»</a></li> </ul> </div> </div> </div> <div class="row"> <div class="col-sm-12"> <ol class="result-class" start="241"> <li> <p><a target="_blank" rel="noopener noreferrer" onclick="trackOutboundLink('http://hdl.handle.net/2060/20160003391','NASA-TRS'); return false;" href="http://hdl.handle.net/2060/20160003391"><span>Technical Report Series on Global Modeling and Data Assimilation. Volume 42; Soil Moisture Active Passive (SMAP) Project Calibration and Validation for the L4_C Beta-Release Data Product</span></a></p> <p><a target="_blank" rel="noopener noreferrer" href="http://ntrs.nasa.gov/search.jsp">NASA Technical Reports Server (NTRS)</a></p> <p>Koster, Randal D. (Editor); Kimball, John S.; Jones, Lucas A.; Glassy, Joseph; Stavros, E. Natasha; Madani, Nima (Editor); Reichle, Rolf H.; Jackson, Thomas; Colliander, Andreas</p> <p>2015-01-01</p> <p>During the post-launch Cal/Val Phase of SMAP there are two objectives for each science product team: 1) calibrate, verify, and improve the performance of the science algorithms, and 2) validate accuracies of the science data products as specified in the L1 science requirements according to the Cal/Val timeline. This report provides analysis and assessment of the SMAP Level 4 Carbon (L4_C) product specifically for the beta release. The beta-release version of the SMAP L4_C algorithms utilizes a terrestrial carbon flux model informed by SMAP soil moisture inputs along with optical remote sensing (e.g. MODIS) vegetation indices and other ancillary biophysical data to estimate global daily NEE and component carbon fluxes, particularly vegetation gross primary production (GPP) and ecosystem respiration (Reco). Other L4_C product elements include surface (<10 cm depth) soil organic carbon (SOC) stocks and associated environmental constraints to these processes, including soil moisture and landscape FT controls on GPP and Reco (Kimball et al. 2012). The L4_C product encapsulates SMAP carbon cycle science objectives by: 1) providing a direct link between terrestrial carbon fluxes and underlying freeze/thaw and soil moisture constraints to these processes, 2) documenting primary connections between terrestrial water, energy and carbon cycles, and 3) improving understanding of terrestrial carbon sink activity in northern ecosystems.</p> </li> <li> <p><a target="_blank" rel="noopener noreferrer" onclick="trackOutboundLink('http://adsabs.harvard.edu/abs/2010AGUFM.B33K..01F','NASAADS'); return false;" href="http://adsabs.harvard.edu/abs/2010AGUFM.B33K..01F"><span>New Insights into an Old Cycle: The Marine Phosphorus Cycle and the Formation of Critical Phosphate Rock Resources (Invited)</span></a></p> <p><a target="_blank" rel="noopener noreferrer" href="http://adsabs.harvard.edu/abstract_service.html">NASA Astrophysics Data System (ADS)</a></p> <p>Filippelli, G. M.</p> <p>2010-12-01</p> <p>The cycling and geochemistry of phosphorus (P) in the marine environment is a critical component of biological productivity and of resource availability: P control the long-term carbon cycle via its role as a limiting nutrient, and the burial and concentration of P within marine sediments dictates the quality and availability of P as a fertilizer component from a resources standpoint. Given the projections of severe P fertilizer limitation over the next several centuries, understanding the controls on P geochemistry and concentration into a minable resource is critical in sustaining global populations. Several critical aspects of the marine P cycle have been uncovered over the past few decades which have clarified our understanding of P burial and concentration. First, the initial authigenic process of P mineralization within marine sediments, termed phosphogenesis, seems to occur regardless of marine setting. Phosphogenesis results from the release of P into sedimentary pore waters from organic and oxide-bound fractions, and the subsequent supersaturation with respect to carbonate fluorapatite. In sediment-starved basins with significant upwelling-driven productivity, the supply of P into sedimentary pore waters can be so high that visibly apparent layers of carbonate fluorapatite can be formed. Even in such environments, however, the mineral P content is too low to be of economic value unless it has undergone concentration via sediment reworking, a common occurrence in some dynamic continental margin environments. Thus, a combination of phosphogenesis in a high productivity setting plus sediment starvation plus condensation via reworking are necessary to produce phosphorites, sedimentary rocks with high P contents which are ideal as fertilizer-grade P resources. Given these special marine conditions, phosphorites are largely distributed along ancient marine environments (with the exception of the nearly-depleted atoll guano reserves). The largest currently-identified minable reservoirs of ore-grade P are found in the United States, in China, and in Morocco. Numerous less-economic sedimentary deposits exist, but these deposits are more dilute and represent former marine settings without the trifecta of productivity, geochemistry and sedimentology that makes phosphorites economically viable.</p> </li> <li> <p><a target="_blank" rel="noopener noreferrer" onclick="trackOutboundLink('http://adsabs.harvard.edu/abs/2007AGUFM.H44C..06G','NASAADS'); return false;" href="http://adsabs.harvard.edu/abs/2007AGUFM.H44C..06G"><span>Spatially explicit simulation of hydrologically controlled carbon and nitrogen cycles and associated feedback mechanisms in a boreal ecosystem in Eastern Canada.</span></a></p> <p><a target="_blank" rel="noopener noreferrer" href="http://adsabs.harvard.edu/abstract_service.html">NASA Astrophysics Data System (ADS)</a></p> <p>Govind, A.; Chen, J. M.; Margolis, H.</p> <p>2007-12-01</p> <p>Current estimates of terrestrial carbon overlook the effects of topographically-driven lateral flow of soil water. We hypothesize that this component, which occur at a landscape or watershed scale have significant influences on the spatial distribution of carbon, due to its large contribution to the local water balance. To this end, we further developed a spatially explicit ecohydrological model, BEPS-TerrainLab V2.0. We simulated the coupled hydrological and carbon cycle processes in a black spruce-moss ecosystem in central Quebec, Canada. The carbon stocks were initialized using a long term carbon cycling model, InTEC, under a climate change and disturbance scenario, the accuracy of which was determined with inventory plot measurements. Further, we simulated and validated several ecosystem indicators such as ET, GPP, NEP, water table, snow depth and soil temperature, using the measurements for two years, 2004 and 2005. After gaining confidence in the model's ability to simulate ecohydrological processes, we tested the influence of lateral water flow on the carbon cycle. We made three hydrological modeling scenarios 1) Explicit, were realistic lateral water routing was considered 2) Implicit where calculations were based on a bucket modeling approach 3) NoFlow, where the lateral water flow was turned off in the model. The results showed that pronounced anomalies exist among the scenarios for the simulated GPP, ET and NEP. In general, Implicit calculation overestimated GPP and underestimated NEP, as opposed to Explicit simulation. NoFlow underestimated GPP and overestimated NEP. The key processes controlling GPP were manifested through stomatal conductance which reduces under conditions of rapid soil saturation ( NoFlow ) or increases in the Implicit case, and, nitrogen availability which affects Vcmax, the maximum carboxylation rate. However, for NEP, the anomalies were attributed to differences in soil carbon pool decomposition, which determine the heterotrophic respiration and the resultant nitrogen mineralization which affects GPP and several other feedback mechanisms. These results suggest that lateral water flow does play a significant role in the terrestrial carbon distribution. Therefore, regional or global scale terrestrial carbon estimates could have significant errors if proper hydrological constrains are not considered for modeling ecological processes due to large topographic variations on the Earth's surface. For more info please visit: http://ajit.govind.googlepages.com/agu2007</p> </li> <li> <p><a target="_blank" rel="noopener noreferrer" onclick="trackOutboundLink('http://adsabs.harvard.edu/abs/2013EGUGA..15.6951B','NASAADS'); return false;" href="http://adsabs.harvard.edu/abs/2013EGUGA..15.6951B"><span>Long term effects of fire on the carbon balance in boreal forests</span></a></p> <p><a target="_blank" rel="noopener noreferrer" href="http://adsabs.harvard.edu/abstract_service.html">NASA Astrophysics Data System (ADS)</a></p> <p>Berninger, Frank; Köster, Kaja; Pumpanen, Jukka</p> <p>2013-04-01</p> <p>Fire is the primary process which organizes the physical and biological attributes of the boreal biome and influences energy flows and biogeochemical cycles, particularly the carbon and nitrogen cycle. We established a forest fire chronosequence in the northern boreal forest in Lapland (Värriö Strict Nature Reserve), Finland (67°46' N, 29°35' E) that spans 160 years. Soil organic matter and its turnover were measured in and ex situ, as well as biomass of trees. The fungal biomass was assessed using soil ergosterol contents. The results indicate that fires slow down the turnover of soil organic matter for a period of at least 50 years. The turnover rate in recently burnt sites was only half of the turnover of the old forest site. Decreases in the turnover where still substantial 50 years after fire. The slow recovery of fungal biomass after fires seems to be the cause of the decrease since sites with a higher concentration of fungal biomass in the soils had shorter soil organic matter turnover rates. Increases in stand foliar biomass were less important for the turnover of soil organic matter. We tried to explore the potential importance of our finding using a simple data driven simulation model that estimates soil carbon dynamic from litter input and the measured soil carbon turnover times. The results indicate the initial post-fire slowdown of soil carbon turnover is an important component of the boreal carbon cycle. Using our fire intervals the simulated soil carbon stocks with a lower post-fire soil organic matter turnover were up to 15 % larger than simulations assuming a constant carbon turnover rate. Our sensitivity analysis indicates that the effects will be larger in areas with frequent fires. We do not know which environmental factors cause the delay in the turnover time and the effects of fires on post fire soil organic matter turnover could be considerably smaller or larger. Altogether our results fit well to published results from laboratory studies and show that post-fire depression of microbial activities are important on the ecosystem and landscape level. Since fire frequencies in boreal forests will increase in many areas as the result of climate change, it will be important to better understand the effects of fire on the soil carbon turnover and to incorporate it into carbon cycle models.</p> </li> <li> <p><a target="_blank" rel="noopener noreferrer" onclick="trackOutboundLink('https://www.ncbi.nlm.nih.gov/pubmed/29902650','PUBMED'); return false;" href="https://www.ncbi.nlm.nih.gov/pubmed/29902650"><span>Diesel fuel blending components from mixture of waste animal fat and light cycle oil from fluid catalytic cracking.</span></a></p> <p><a target="_blank" rel="noopener noreferrer" href="https://www.ncbi.nlm.nih.gov/entrez/query.fcgi?DB=pubmed">PubMed</a></p> <p>Hancsók, Jenő; Sági, Dániel; Valyon, József</p> <p>2018-06-11</p> <p>Sustainable production of renewable fuels has become an imperative goal but also remains a huge challenge faced by the chemical industry. A variety of low-value, renewable sources of carbon such as wastes and by-products must be evaluated for their potential as feedstock to achieve this goal. Hydrogenation of blends comprising waste animal fat (≤70 wt%) and low-value fluid catalytic cracking light cycle oil (≥30 wt%), with a total aromatic content of 87.2 wt%, was studied on a commercial sulfided NiMo/Al 2 O 3 catalyst. The fuel fraction in the diesel boiling range was separated by fractional distillation from the organic liquid product obtained from the catalytic conversion of the blend of 70 wt% waste animal fat and 30 wt% light cycle oil. Diesel fuel of the best quality was obtained under the following reaction conditions: T = 615-635 K, P = 6 MPa, LHSV = 1.0 h -1 , H 2 /feedstock ratio = 600 Nm 3 /m 3 . The presence of fat in the feedstock was found to promote the conversion of light cycle oil to a paraffinic blending component for diesel fuel. Thus, a value-added alternative fuel with high biocontent can be obtained from low-value refinery stream and waste animal fat. The resultant disposal of waste animal fat, and the use of fuel containing less fossil carbon for combustion helps reduce the emission of pollutants. Copyright © 2018 Elsevier Ltd. All rights reserved.</p> </li> <li> <p><a target="_blank" rel="noopener noreferrer" onclick="trackOutboundLink('https://www.osti.gov/pages/biblio/1198482-variable-stoichiometry-dissolved-organic-matter-cycling-community-earth-system-model','SCIGOV-DOEP'); return false;" href="https://www.osti.gov/pages/biblio/1198482-variable-stoichiometry-dissolved-organic-matter-cycling-community-earth-system-model"><span>Variable C : N : P stoichiometry of dissolved organic matter cycling in the Community Earth System Model</span></a></p> <p><a target="_blank" rel="noopener noreferrer" href="http://www.osti.gov/pages">DOE PAGES</a></p> <p>Letscher, R. T.; Moore, J. K.; Teng, Y. -C.; ...</p> <p>2014-06-16</p> <p>Dissolved organic matter (DOM) plays an important role in the ocean's biological carbon pump by providing an advective/mixing pathway for ~ 20% of export production. DOM is known to have a stoichiometry depleted in nitrogen (N) and phosphorus (P) compared to the particulate organic matter pool, a~fact that is often omitted from biogeochemical-ocean general circulation models. However the variable C : N : P stoichiometry of DOM becomes important when quantifying carbon export from the upper ocean and linking the nutrient cycles of N and P with that of carbon. Here we utilize recent advances in DOM observational data coveragemore » and offline tracer-modeling techniques to objectively constrain the variable production and remineralization rates of the DOM C / N / P pools in a simple biogeochemical-ocean model of DOM cycling. The optimized DOM cycling parameters are then incorporated within the Biogeochemical Elemental Cycling (BEC) component of the Community Earth System Model and validated against the compilation of marine DOM observations. The optimized BEC simulation including variable DOM C : N : P cycling was found to better reproduce the observed DOM spatial gradients than simulations that used the canonical Redfield ratio. Global annual average export of dissolved organic C, N, and P below 100 m was found to be 2.28 Pg C yr -1 (143 Tmol C yr -1), 16.4 Tmol N yr -1, and 1 Tmol P yr -1, respectively with an average export C : N : P stoichiometry of 225 : 19 : 1 for the semilabile (degradable) DOM pool. DOC export contributed ~ 25% of the combined organic C export to depths greater than 100 m.« less</p> </li> <li> <p><a target="_blank" rel="noopener noreferrer" onclick="trackOutboundLink('https://www.osti.gov/servlets/purl/1435490','SCIGOV-STC'); return false;" href="https://www.osti.gov/servlets/purl/1435490"><span>sCO2 Power Cycles Summit Summary November 2017.</span></a></p> <p><a target="_blank" rel="noopener noreferrer" href="http://www.osti.gov/search">DOE Office of Scientific and Technical Information (OSTI.GOV)</a></p> <p>Mendez Cruz, Carmen Margarita; Rochau, Gary E.; Lance, Blake</p> <p></p> <p>Over the past ten years, the Department of Energy (DOE) has helped to develop components and technologies for the Supercritical Carbon Dioxide (sCO2) power cycle capable of efficient operation at high temperatures and high efficiency. The DOE Offices of Fossil Energy, Nuclear Energy, and Energy Efficiency and Renewable Energy collaborated in the planning and execution of the sCO2 Power Cycle Summit conducted in Albuquerque, NM in November 2017. The summit brought together participants from government, national laboratories, research, and industry to engage in discussions regarding the future of sCO 2 Power Cycles Technology. This report summarizes the work involved inmore » summit planning and execution, before, during, and after the event, including the coordination between three DOE offices and technical content presented at the event.« less</p> </li> <li> <p><a target="_blank" rel="noopener noreferrer" onclick="trackOutboundLink('http://onlinelibrary.wiley.com/doi/10.1029/2009GM000914/summary','USGSPUBS'); return false;" href="http://onlinelibrary.wiley.com/doi/10.1029/2009GM000914/summary"><span>An introduction to global carbon cycle management</span></a></p> <p><a target="_blank" rel="noopener noreferrer" href="http://pubs.er.usgs.gov/pubs/index.jsp?view=adv">USGS Publications Warehouse</a></p> <p>Sundquist, Eric T.; Ackerman, Katherine V.; Parker, Lauren; Huntzinger, Deborah N.</p> <p>2009-01-01</p> <p>Past and current human activities have fundamentally altered the global carbon cycle. Potential future efforts to control atmospheric CO2 will also involve significant changes in the global carbon cycle. Carbon cycle scientists and engineers now face not only the difficulties of recording and understanding past and present changes but also the challenge of providing information and tools for new management strategies that are responsive to societal needs. The challenge is nothing less than managing the global carbon cycle.</p> </li> <li> <p><a target="_blank" rel="noopener noreferrer" onclick="trackOutboundLink('https://www.ncbi.nlm.nih.gov/pubmed/14628061','PUBMED'); return false;" href="https://www.ncbi.nlm.nih.gov/pubmed/14628061"><span>The long-term carbon cycle, fossil fuels and atmospheric composition.</span></a></p> <p><a target="_blank" rel="noopener noreferrer" href="https://www.ncbi.nlm.nih.gov/entrez/query.fcgi?DB=pubmed">PubMed</a></p> <p>Berner, Robert A</p> <p>2003-11-20</p> <p>The long-term carbon cycle operates over millions of years and involves the exchange of carbon between rocks and the Earth's surface. There are many complex feedback pathways between carbon burial, nutrient cycling, atmospheric carbon dioxide and oxygen, and climate. New calculations of carbon fluxes during the Phanerozoic eon (the past 550 million years) illustrate how the long-term carbon cycle has affected the burial of organic matter and fossil-fuel formation, as well as the evolution of atmospheric composition.</p> </li> <li> <p><a target="_blank" rel="noopener noreferrer" onclick="trackOutboundLink('https://www.ncbi.nlm.nih.gov/pubmed/21458575','PUBMED'); return false;" href="https://www.ncbi.nlm.nih.gov/pubmed/21458575"><span>Amorphous and crystalline calcium carbonate distribution in the tergite cuticle of moulting Porcellio scaber (Isopoda, Crustacea).</span></a></p> <p><a target="_blank" rel="noopener noreferrer" href="https://www.ncbi.nlm.nih.gov/entrez/query.fcgi?DB=pubmed">PubMed</a></p> <p>Neues, Frank; Hild, Sabine; Epple, Matthias; Marti, Othmar; Ziegler, Andreas</p> <p>2011-07-01</p> <p>The main mineral components of the isopod cuticle consists of crystalline magnesium calcite and amorphous calcium carbonate. During moulting isopods moult first the posterior and then the anterior half of the body. In terrestrial species calcium carbonate is subject to resorption, storage and recycling in order to retain significant fractions of the mineral during the moulting cycle. We used synchrotron X-ray powder diffraction, elemental analysis and Raman spectroscopy to quantify the ACC/calcite ratio, the mineral phase distribution and the composition within the anterior and posterior tergite cuticle during eight different stages of the moulting cycle of Porcellio scaber. The results show that most of the amorphous calcium carbonate (ACC) is resorbed from the cuticle, whereas calcite remains in the old cuticle and is shed during moulting. During premoult resorption of ACC from the posterior cuticle is accompanied by an increase within the anterior tergites, and mineralization of the new posterior cuticle by resorption of mineral from the anterior cuticle. This suggests that one reason for using ACC in cuticle mineralization is to facilitate resorption and recycling of cuticular calcium carbonate. Furthermore we show that ACC precedes the formation of calcite in distal layers of the tergite cuticle. Copyright © 2011 Elsevier Inc. All rights reserved.</p> </li> <li> <p><a target="_blank" rel="noopener noreferrer" onclick="trackOutboundLink('https://www.pubmedcentral.nih.gov/articlerender.fcgi?tool=pmcentrez&artid=4730203','PMC'); return false;" href="https://www.pubmedcentral.nih.gov/articlerender.fcgi?tool=pmcentrez&artid=4730203"><span>Arbuscular mycorrhizal fungi regulate soil respiration and its response to precipitation change in a semiarid steppe</span></a></p> <p><a target="_blank" rel="noopener noreferrer" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?DB=pmc">PubMed Central</a></p> <p>Zhang, Bingwei; Li, Shan; Chen, Shiping; Ren, Tingting; Yang, Zhiqiang; Zhao, Hanlin; Liang, Yu; Han, Xingguo</p> <p>2016-01-01</p> <p>Arbuscular mycorrhizal fungi (AMF) are critical links in plant–soil continuum and play a critical role in soil carbon cycles. Soil respiration, one of the largest carbon fluxes in global carbon cycle, is sensitive to precipitation change in semiarid ecosystems. In this study, a field experiment with fungicide application and water addition was conducted during 2010–2013 in a semiarid steppe in Inner Mongolia, China, and soil respiration was continuously measured to investigate the influences of AMF on soil respiration under different precipitation regimes. Results showed that soil respiration was promoted by water addition treatment especially during drought seasons, which induced a nonlinear response of soil respiration to precipitation change. Fungicide application suppressed AMF root colonization without impacts on soil microbes. AMF suppression treatment accelerated soil respiration with 2.7, 28.5 and 37.6 g C m−2 across three seasons, which were mainly caused by the enhanced heterotrophic component. A steeper response of soil respiration rate to precipitation was found under fungicide application treatments, suggesting a greater dampening effect of AMF on soil carbon release as water availability increased. Our study highlighted the importance of AMF on soil carbon stabilization and sequestration in semiarid steppe ecosystems especially during wet seasons. PMID:26818214</p> </li> <li> <p><a target="_blank" rel="noopener noreferrer" onclick="trackOutboundLink('https://www.ncbi.nlm.nih.gov/pubmed/26818214','PUBMED'); return false;" href="https://www.ncbi.nlm.nih.gov/pubmed/26818214"><span>Arbuscular mycorrhizal fungi regulate soil respiration and its response to precipitation change in a semiarid steppe.</span></a></p> <p><a target="_blank" rel="noopener noreferrer" href="https://www.ncbi.nlm.nih.gov/entrez/query.fcgi?DB=pubmed">PubMed</a></p> <p>Zhang, Bingwei; Li, Shan; Chen, Shiping; Ren, Tingting; Yang, Zhiqiang; Zhao, Hanlin; Liang, Yu; Han, Xingguo</p> <p>2016-01-28</p> <p>Arbuscular mycorrhizal fungi (AMF) are critical links in plant-soil continuum and play a critical role in soil carbon cycles. Soil respiration, one of the largest carbon fluxes in global carbon cycle, is sensitive to precipitation change in semiarid ecosystems. In this study, a field experiment with fungicide application and water addition was conducted during 2010-2013 in a semiarid steppe in Inner Mongolia, China, and soil respiration was continuously measured to investigate the influences of AMF on soil respiration under different precipitation regimes. Results showed that soil respiration was promoted by water addition treatment especially during drought seasons, which induced a nonlinear response of soil respiration to precipitation change. Fungicide application suppressed AMF root colonization without impacts on soil microbes. AMF suppression treatment accelerated soil respiration with 2.7, 28.5 and 37.6 g C m(-2) across three seasons, which were mainly caused by the enhanced heterotrophic component. A steeper response of soil respiration rate to precipitation was found under fungicide application treatments, suggesting a greater dampening effect of AMF on soil carbon release as water availability increased. Our study highlighted the importance of AMF on soil carbon stabilization and sequestration in semiarid steppe ecosystems especially during wet seasons.</p> </li> <li> <p><a target="_blank" rel="noopener noreferrer" onclick="trackOutboundLink('https://www.pubmedcentral.nih.gov/articlerender.fcgi?tool=pmcentrez&artid=5474806','PMC'); return false;" href="https://www.pubmedcentral.nih.gov/articlerender.fcgi?tool=pmcentrez&artid=5474806"><span>Historical climate controls soil respiration responses to current soil moisture</span></a></p> <p><a target="_blank" rel="noopener noreferrer" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?DB=pmc">PubMed Central</a></p> <p>Waring, Bonnie G.; Rocca, Jennifer D.; Kivlin, Stephanie N.</p> <p>2017-01-01</p> <p>Ecosystem carbon losses from soil microbial respiration are a key component of global carbon cycling, resulting in the transfer of 40–70 Pg carbon from soil to the atmosphere each year. Because these microbial processes can feed back to climate change, understanding respiration responses to environmental factors is necessary for improved projections. We focus on respiration responses to soil moisture, which remain unresolved in ecosystem models. A common assumption of large-scale models is that soil microorganisms respond to moisture in the same way, regardless of location or climate. Here, we show that soil respiration is constrained by historical climate. We find that historical rainfall controls both the moisture dependence and sensitivity of respiration. Moisture sensitivity, defined as the slope of respiration vs. moisture, increased fourfold across a 480-mm rainfall gradient, resulting in twofold greater carbon loss on average in historically wetter soils compared with historically drier soils. The respiration–moisture relationship was resistant to environmental change in field common gardens and field rainfall manipulations, supporting a persistent effect of historical climate on microbial respiration. Based on these results, predicting future carbon cycling with climate change will require an understanding of the spatial variation and temporal lags in microbial responses created by historical rainfall. PMID:28559315</p> </li> <li> <p><a target="_blank" rel="noopener noreferrer" onclick="trackOutboundLink('http://adsabs.harvard.edu/abs/2016NatSR...619990Z','NASAADS'); return false;" href="http://adsabs.harvard.edu/abs/2016NatSR...619990Z"><span>Arbuscular mycorrhizal fungi regulate soil respiration and its response to precipitation change in a semiarid steppe</span></a></p> <p><a target="_blank" rel="noopener noreferrer" href="http://adsabs.harvard.edu/abstract_service.html">NASA Astrophysics Data System (ADS)</a></p> <p>Zhang, Bingwei; Li, Shan; Chen, Shiping; Ren, Tingting; Yang, Zhiqiang; Zhao, Hanlin; Liang, Yu; Han, Xingguo</p> <p>2016-01-01</p> <p>Arbuscular mycorrhizal fungi (AMF) are critical links in plant-soil continuum and play a critical role in soil carbon cycles. Soil respiration, one of the largest carbon fluxes in global carbon cycle, is sensitive to precipitation change in semiarid ecosystems. In this study, a field experiment with fungicide application and water addition was conducted during 2010-2013 in a semiarid steppe in Inner Mongolia, China, and soil respiration was continuously measured to investigate the influences of AMF on soil respiration under different precipitation regimes. Results showed that soil respiration was promoted by water addition treatment especially during drought seasons, which induced a nonlinear response of soil respiration to precipitation change. Fungicide application suppressed AMF root colonization without impacts on soil microbes. AMF suppression treatment accelerated soil respiration with 2.7, 28.5 and 37.6 g C m-2 across three seasons, which were mainly caused by the enhanced heterotrophic component. A steeper response of soil respiration rate to precipitation was found under fungicide application treatments, suggesting a greater dampening effect of AMF on soil carbon release as water availability increased. Our study highlighted the importance of AMF on soil carbon stabilization and sequestration in semiarid steppe ecosystems especially during wet seasons.</p> </li> <li> <p><a target="_blank" rel="noopener noreferrer" onclick="trackOutboundLink('http://adsabs.harvard.edu/abs/2016JGRC..121.7973L','NASAADS'); return false;" href="http://adsabs.harvard.edu/abs/2016JGRC..121.7973L"><span>Chromophoric and fluorescent dissolved organic matter in and above the oxygen minimum zone off Peru</span></a></p> <p><a target="_blank" rel="noopener noreferrer" href="http://adsabs.harvard.edu/abstract_service.html">NASA Astrophysics Data System (ADS)</a></p> <p>Loginova, A. N.; Thomsen, S.; Engel, A.</p> <p>2016-11-01</p> <p>As a result of nutrient upwelling, the Peruvian coastal system is one of the most productive regions in the ocean. Sluggish ventilation of intermediate waters, characteristic for the Eastern Tropical South Pacific (ETSP) and microbial degradation of a high organic matter load promotes deoxygenation at depth. Dissolved organic matter (DOM) plays a key role in microbial respiration and carbon cycling, but little is known on DOM distribution and cycling in the ETSP. DOM optical properties give important insights on DOM sources, structure and biogeochemical reactivity. Here, we present data and a conceptual view on distribution and cycling of chromophoric (CDOM) and fluorescent (FDOM) DOM in and above the oxygen minimum zone (OMZ) off Peru. Five fluorescent components were identified during PARAFAC analysis. Highest intensities of CDOM and of the amino acid-like fluorescent component (C3) occurred above the OMZ and coincided with maximum chl a concentrations, suggesting phytoplankton productivity as major source. High intensities of a marine humic-like fluorescent component (C1), observed in subsurface waters, indicated in situ microbial reworking of DOM. FDOM release from inner shelf sediment was determined by seawater analysis and continuous glider sensor measurement and included a humic-like component (C2) with a signature typical for terrestrially derived humic acids. Upwelling supplied humic-like substances to the euphotic zone. Photo-reactions were likely involved in the production of a humic-like fluorescent component (C5). Our data show that variable biological and physical processes need to be considered for understanding DOM cycling in a highly dynamic coastal upwelling system like the ETSP off Peru.</p> </li> <li> <p><a target="_blank" rel="noopener noreferrer" onclick="trackOutboundLink('http://www.osti.gov/sciencecinema/biblio/1015183','SCIGOVIMAGE-SCICINEMA'); return false;" href="http://www.osti.gov/sciencecinema/biblio/1015183"><span>Solar Fuels and Carbon Cycle 2.0 (Carbon Cycle 2.0)</span></a></p> <p><a target="_blank" rel="noopener noreferrer" href="http://www.osti.gov/sciencecinema/">ScienceCinema</a></p> <p>Alivisatos, Paul</p> <p>2018-05-08</p> <p>Paul Alivisatos, LBNL Director speaks at the Carbon Cycle 2.0 kick-off symposium Feb. 4, 2010. We emit more carbon into the atmosphere than natural processes are able to remove - an imbalance with negative consequences. Carbon Cycle 2.0 is a Berkeley Lab initiative to provide the science needed to restore this balance by integrating the Labs diverse research activities and delivering creative solutions toward a carbon-neutral energy future.</p> </li> <li> <p><a target="_blank" rel="noopener noreferrer" onclick="trackOutboundLink('https://www.ncbi.nlm.nih.gov/pubmed/25548163','PUBMED'); return false;" href="https://www.ncbi.nlm.nih.gov/pubmed/25548163"><span>Cryptic carbon and sulfur cycling between surface ocean plankton.</span></a></p> <p><a target="_blank" rel="noopener noreferrer" href="https://www.ncbi.nlm.nih.gov/entrez/query.fcgi?DB=pubmed">PubMed</a></p> <p>Durham, Bryndan P; Sharma, Shalabh; Luo, Haiwei; Smith, Christa B; Amin, Shady A; Bender, Sara J; Dearth, Stephen P; Van Mooy, Benjamin A S; Campagna, Shawn R; Kujawinski, Elizabeth B; Armbrust, E Virginia; Moran, Mary Ann</p> <p>2015-01-13</p> <p>About half the carbon fixed by phytoplankton in the ocean is taken up and metabolized by marine bacteria, a transfer that is mediated through the seawater dissolved organic carbon (DOC) pool. The chemical complexity of marine DOC, along with a poor understanding of which compounds form the basis of trophic interactions between bacteria and phytoplankton, have impeded efforts to identify key currencies of this carbon cycle link. Here, we used transcriptional patterns in a bacterial-diatom model system based on vitamin B12 auxotrophy as a sensitive assay for metabolite exchange between marine plankton. The most highly up-regulated genes (up to 374-fold) by a marine Roseobacter clade bacterium when cocultured with the diatom Thalassiosira pseudonana were those encoding the transport and catabolism of 2,3-dihydroxypropane-1-sulfonate (DHPS). This compound has no currently recognized role in the marine microbial food web. As the genes for DHPS catabolism have limited distribution among bacterial taxa, T. pseudonana may use this sulfonate for targeted feeding of beneficial associates. Indeed, DHPS was both a major component of the T. pseudonana cytosol and an abundant microbial metabolite in a diatom bloom in the eastern North Pacific Ocean. Moreover, transcript analysis of the North Pacific samples provided evidence of DHPS catabolism by Roseobacter populations. Other such biogeochemically important metabolites may be common in the ocean but difficult to discriminate against the complex chemical background of seawater. Bacterial transformation of this diatom-derived sulfonate represents a previously unidentified and likely sizeable link in both the marine carbon and sulfur cycles.</p> </li> <li> <p><a target="_blank" rel="noopener noreferrer" onclick="trackOutboundLink('http://adsabs.harvard.edu/abs/2018ESD.....9..507L','NASAADS'); return false;" href="http://adsabs.harvard.edu/abs/2018ESD.....9..507L"><span>Analytically tractable climate-carbon cycle feedbacks under 21st century anthropogenic forcing</span></a></p> <p><a target="_blank" rel="noopener noreferrer" href="http://adsabs.harvard.edu/abstract_service.html">NASA Astrophysics Data System (ADS)</a></p> <p>Lade, Steven J.; Donges, Jonathan F.; Fetzer, Ingo; Anderies, John M.; Beer, Christian; Cornell, Sarah E.; Gasser, Thomas; Norberg, Jon; Richardson, Katherine; Rockström, Johan; Steffen, Will</p> <p>2018-05-01</p> <p>Changes to climate-carbon cycle feedbacks may significantly affect the Earth system's response to greenhouse gas emissions. These feedbacks are usually analysed from numerical output of complex and arguably opaque Earth system models. Here, we construct a stylised global climate-carbon cycle model, test its output against comprehensive Earth system models, and investigate the strengths of its climate-carbon cycle feedbacks analytically. The analytical expressions we obtain aid understanding of carbon cycle feedbacks and the operation of the carbon cycle. Specific results include that different feedback formalisms measure fundamentally the same climate-carbon cycle processes; temperature dependence of the solubility pump, biological pump, and CO2 solubility all contribute approximately equally to the ocean climate-carbon feedback; and concentration-carbon feedbacks may be more sensitive to future climate change than climate-carbon feedbacks. Simple models such as that developed here also provide <q>workbenches</q> for simple but mechanistically based explorations of Earth system processes, such as interactions and feedbacks between the planetary boundaries, that are currently too uncertain to be included in comprehensive Earth system models.</p> </li> <li> <p><a target="_blank" rel="noopener noreferrer" onclick="trackOutboundLink('https://www.ncbi.nlm.nih.gov/pubmed/28299860','PUBMED'); return false;" href="https://www.ncbi.nlm.nih.gov/pubmed/28299860"><span>Poly(3-hydroxybutyrate) fuels the tricarboxylic acid cycle and de novo lipid biosynthesis during Bacillus anthracis sporulation.</span></a></p> <p><a target="_blank" rel="noopener noreferrer" href="https://www.ncbi.nlm.nih.gov/entrez/query.fcgi?DB=pubmed">PubMed</a></p> <p>Sadykov, Marat R; Ahn, Jong-Sam; Widhelm, Todd J; Eckrich, Valerie M; Endres, Jennifer L; Driks, Adam; Rutkowski, Gregory E; Wingerd, Kevin L; Bayles, Kenneth W</p> <p>2017-06-01</p> <p>Numerous bacteria accumulate poly(3-hydroxybutyrate) (PHB) as an intracellular reservoir of carbon and energy in response to imbalanced nutritional conditions. In Bacillus spp., where PHB biosynthesis precedes the formation of the dormant cell type called the spore (sporulation), the direct link between PHB accumulation and efficiency of sporulation was observed in multiple studies. Although the idea of PHB as an intracellular carbon and energy source fueling sporulation was proposed several decades ago, the mechanisms underlying PHB contribution to sporulation have not been defined. Here, we demonstrate that PHB deficiency impairs Bacillus anthracis sporulation through diminishing the energy status of the cells and by reducing carbon flux into the tricarboxylic acid (TCA) cycle and de novo lipid biosynthesis. Consequently, this metabolic imbalance decreased biosynthesis of the critical components required for spore integrity and resistance, such as dipicolinic acid (DPA) and the spore's inner membrane. Supplementation of the PHB deficient mutant with exogenous fatty acids overcame these sporulation defects, highlighting the importance of the TCA cycle and lipid biosynthesis during sporulation. Combined, the results of this work reveal the molecular mechanisms of PHB contribution to B. anthracis sporulation and provide valuable insight into the metabolic requirements for this developmental process in Bacillus species. © 2017 John Wiley & Sons Ltd.</p> </li> <li> <p><a target="_blank" rel="noopener noreferrer" onclick="trackOutboundLink('http://adsabs.harvard.edu/abs/2015JPS...296..454J','NASAADS'); return false;" href="http://adsabs.harvard.edu/abs/2015JPS...296..454J"><span>Fair performance comparison of different carbon blacks in lithium-sulfur batteries with practical mass loadings - Simple design competes with complex cathode architecture</span></a></p> <p><a target="_blank" rel="noopener noreferrer" href="http://adsabs.harvard.edu/abstract_service.html">NASA Astrophysics Data System (ADS)</a></p> <p>Jozwiuk, Anna; Sommer, Heino; Janek, Jürgen; Brezesinski, Torsten</p> <p>2015-11-01</p> <p>The lithium-sulfur system is one of the most promising next generation battery systems, as elemental sulfur is cheap, abundant and has a high theoretical specific capacity. Although much research is conducted on complex sulfur/carbon composites and architectures, it is difficult to compare the performance of the cathodes to one another. Factors, such as different electrolyte composition and cell components strongly affect the cyclability of the battery. Here, we show the importance of optimizing ;standard; conditions to allow for fair performance comparison of different carbon blacks. Our optimal electrolyte-to-sulfur ratio is 11 μL mgsulfur-1 and high concentrations of LiNO3 (>0.6 M) are needed because nitrate is consumed continuously during cycling. Utilizing these standard conditions, we tested the cycling behavior of four types of cathodes with individual carbon blacks having different specific surface areas, namely Printex-A, Super C65, Printex XE-2 and Ketjenblack EC-600JD. Both the specific capacity and polysulfide adsorption capability clearly correlate with the surface area of the carbon being used. High specific capacities (>1000 mAh gsulfur-1 at C/5) are achieved with high surface area carbons. We also demonstrate that a simple cathode using Ketjenblack EC-600JD as the conductive matrix material can well compete with those having complex architectures or additives.</p> </li> </ol> <div class="pull-right"> <ul class="pagination"> <li><a href="#" onclick='return showDiv("page_1");'>«</a></li> <li><a href="#" onclick='return showDiv("page_11");'>11</a></li> <li><a href="#" onclick='return showDiv("page_12");'>12</a></li> <li class="active"><span>13</span></li> <li><a href="#" onclick='return showDiv("page_14");'>14</a></li> <li><a href="#" onclick='return showDiv("page_15");'>15</a></li> <li><a href="#" onclick='return showDiv("page_25");'>»</a></li> </ul> </div> </div><!-- col-sm-12 --> </div><!-- row --> </div><!-- page_13 --> <div id="page_14" class="hiddenDiv"> <div class="row"> <div class="col-sm-12"> <div class="pull-right"> <ul class="pagination"> <li><a href="#" onclick='return showDiv("page_1");'>«</a></li> <li><a href="#" onclick='return showDiv("page_12");'>12</a></li> <li><a href="#" onclick='return showDiv("page_13");'>13</a></li> <li class="active"><span>14</span></li> <li><a href="#" onclick='return showDiv("page_15");'>15</a></li> <li><a href="#" onclick='return showDiv("page_16");'>16</a></li> <li><a href="#" onclick='return showDiv("page_25");'>»</a></li> </ul> </div> </div> </div> <div class="row"> <div class="col-sm-12"> <ol class="result-class" start="261"> <li> <p><a target="_blank" rel="noopener noreferrer" onclick="trackOutboundLink('https://www.fs.usda.gov/treesearch/pubs/45433','TREESEARCH'); return false;" href="https://www.fs.usda.gov/treesearch/pubs/45433"><span>Chapter 6: New Products and Product Categories in the Global Forest Sector</span></a></p> <p><a target="_blank" rel="noopener noreferrer" href="http://www.fs.usda.gov/treesearch/">Treesearch</a></p> <p>Zhiyong Cai; Alan W. Rudie; Nicole M. Stark; Ronald C. Sabo; Sally A. Ralph</p> <p>2013-01-01</p> <p>Forests, covering about 30% of the earthâs land area, are a major component in the global ecosystem, influencing the carbon cycle, climate change, habitat protection, clean water supplies, and sustainable economies (FAO 2011). Globally, the vast cellulosic resource found in forests provides about half of all major industrial raw materials for renewable energy, chemical...</p> </li> <li> <p><a target="_blank" rel="noopener noreferrer" onclick="trackOutboundLink('https://www.pubmedcentral.nih.gov/articlerender.fcgi?tool=pmcentrez&artid=4705541','PMC'); return false;" href="https://www.pubmedcentral.nih.gov/articlerender.fcgi?tool=pmcentrez&artid=4705541"><span>Anaerobic decomposition of humic substances by Clostridium from the deep subsurface</span></a></p> <p><a target="_blank" rel="noopener noreferrer" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?DB=pmc">PubMed Central</a></p> <p>Ueno, Akio; Shimizu, Satoru; Tamamura, Shuji; Okuyama, Hidetoshi; Naganuma, Takeshi; Kaneko, Katsuhiko</p> <p>2016-01-01</p> <p>Decomposition of humic substances (HSs) is a slow and cryptic but non-negligible component of carbon cycling in sediments. Aerobic decomposition of HSs by microorganisms in the surface environment has been well documented; however, the mechanism of anaerobic microbial decomposition of HSs is not completely understood. Moreover, no microorganisms capable of anaerobic decomposition of HSs have been isolated. Here, we report the anaerobic decomposition of humic acids (HAs) by the anaerobic bacterium Clostridium sp. HSAI-1 isolated from the deep terrestrial subsurface. The use of 14C-labelled polycatechol as an HA analogue demonstrated that the bacterium decomposed this substance up to 7.4% over 14 days. The decomposition of commercial and natural HAs by the bacterium yielded lower molecular mass fractions, as determined using high-performance size-exclusion chromatography. Fourier transform infrared spectroscopy revealed the removal of carboxyl groups and polysaccharide-related substances, as well as the generation of aliphatic components, amide and aromatic groups. Therefore, our results suggest that Clostridium sp. HSAI-1 anaerobically decomposes and transforms HSs. This study improves our understanding of the anaerobic decomposition of HSs in the hidden carbon cycling in the Earth’s subsurface. PMID:26743007</p> </li> <li> <p><a target="_blank" rel="noopener noreferrer" onclick="trackOutboundLink('http://hdl.handle.net/2060/20050217167','NASA-TRS'); return false;" href="http://hdl.handle.net/2060/20050217167"><span>High-Temperature Polymer Composites Tested for Hypersonic Rocket Combustor Backup Structure</span></a></p> <p><a target="_blank" rel="noopener noreferrer" href="http://ntrs.nasa.gov/search.jsp">NASA Technical Reports Server (NTRS)</a></p> <p>Sutter, James K.; Shin, E. Eugene; Thesken, John C.; Fink, Jeffrey E.</p> <p>2005-01-01</p> <p>Significant component weight reductions are required to achieve the aggressive thrust-toweight goals for the Rocket Based Combined Cycle (RBCC) third-generation, reusable liquid propellant rocket engine, which is one possible engine for a future single-stage-toorbit vehicle. A collaboration between the NASA Glenn Research Center and Boeing Rocketdyne was formed under the Higher Operating Temperature Propulsion Components (HOTPC) program and, currently, the Ultra-Efficient Engine Technology (UEET) Project to develop carbon-fiber-reinforced high-temperature polymer matrix composites (HTPMCs). This program focused primarily on the combustor backup structure to replace all metallic support components with a much lighter polymer-matrixcomposite- (PMC-) titanium honeycomb sandwich structure.</p> </li> <li> <p><a target="_blank" rel="noopener noreferrer" onclick="trackOutboundLink('http://adsabs.harvard.edu/abs/2017AGUFM.H23I1791B','NASAADS'); return false;" href="http://adsabs.harvard.edu/abs/2017AGUFM.H23I1791B"><span>The carbon commute: Effects of urbanization on dissolved organic carbon quality on a suburban New England river network</span></a></p> <p><a target="_blank" rel="noopener noreferrer" href="http://adsabs.harvard.edu/abstract_service.html">NASA Astrophysics Data System (ADS)</a></p> <p>Balch, E.; Robison, A.; Wollheim, W. M.</p> <p>2017-12-01</p> <p>Understanding anthropogenic influence on the sources and fluxes of carbon is necessary for interpreting the carbon cycle and contaminant transport throughout a river system. As urbanization increases worldwide, it is critical to understand how urbanization affects the carbon cycle so that we may be able to predict future changes. Rivers act as both transporters of terrestrial dissolved organic carbon (DOC) to coastal regions, and active transformers of DOC. The character (lability) of the carbon found within a river network is influenced by its sources and fluxes, as determined by the ecological processes, land use, and discharge, which vary throughout the network. We have characterized DOC quantity and quality throughout a suburban New England river network (Ipswich River, MA) in an attempt to provide a detailed picture of how DOC quality varies within a network, and how urbanization influences these changes. We conducted a synoptic survey of 45 sites over two hydrologically similar days in the Ipswich River network in northeast Massachusetts, USA. We collected discrete grab samples for DOC quantity and quality analyses. We also collected dissolved oxygen, conductivity, and nutrients (major anions and cations) as an extension of the synoptic survey. We plan to determine the source of the DOC by using excitation-emission matrices (EEMs), and specific UV absorption (SUVA) at 254 nm. These analyses will provide us with a detailed picture of how DOC quality varies within a network, and how urbanization influences these changes. Using land use data of the Ipswich River watershed, we are able to model the changes in DOC quality throughout the network. In highly urbanized headwaters, through the progressively more forested and wetland dominated main stem reaches, we expect to see the imprint of urbanization throughout the network due to its decreased lability. Studying the imprint of urbanization on DOC throughout a river network helps us complete our understanding of freshwater carbon processes. Rivers are an important component of the global carbon balance, and monitoring the effect of urbanization on the carbon cycle in freshwater systems is integral to understanding their role in the global carbon system.</p> </li> <li> <p><a target="_blank" rel="noopener noreferrer" onclick="trackOutboundLink('https://www.osti.gov/pages/biblio/1372999-analysis-terrestrial-aquatic-environmental-controls-riverine-dissolved-organic-carbon-conterminous-united-states','SCIGOV-DOEP'); return false;" href="https://www.osti.gov/pages/biblio/1372999-analysis-terrestrial-aquatic-environmental-controls-riverine-dissolved-organic-carbon-conterminous-united-states"><span>An Analysis of Terrestrial and Aquatic Environmental Controls of Riverine Dissolved Organic Carbon in the Conterminous United States</span></a></p> <p><a target="_blank" rel="noopener noreferrer" href="http://www.osti.gov/pages">DOE PAGES</a></p> <p>Yang, Qichun; Zhang, Xuesong; Xu, Xingya; ...</p> <p>2017-05-29</p> <p>Riverine carbon cycling is an important, but insufficiently investigated component of the global carbon cycle. Analyses of environmental controls on riverine carbon cycling are critical for improved understanding of mechanisms regulating carbon processing and storage along the terrestrial-aquatic continuum. Here, we compile and analyze riverine dissolved organic carbon (DOC) concentration data from 1402 United States Geological Survey (USGS) gauge stations to examine the spatial variability and environmental controls of DOC concentrations in the United States (U.S.) surface waters. DOC concentrations exhibit high spatial variability, with an average of 6.42 ± 6.47 mg C/ L (Mean ± Standard Deviation). In general,more » high DOC concentrations occur in the Upper Mississippi River basin and the Southeastern U.S., while low concentrations are mainly distributed in the Western U.S. Single-factor analysis indicates that slope of drainage areas, wetlands, forests, percentage of first-order streams, and instream nutrients (such as nitrogen and phosphorus) pronouncedly influence DOC concentrations, but the explanatory power of each bivariate model is lower than 35%. Analyses based on the general multi-linear regression models suggest DOC concentrations are jointly impacted by multiple factors. Soil properties mainly show positive correlations with DOC concentrations; forest and shrub lands have positive correlations with DOC concentrations, but urban area and croplands demonstrate negative impacts; total instream phosphorus and dam density correlate positively with DOC concentrations. Notably, the relative importance of these environmental controls varies substantially across major U.S. water resource regions. In addition, DOC concentrations and environmental controls also show significant variability from small streams to large rivers, which may be caused by changing carbon sources and removal rates by river orders. In sum, our results reveal that general multi-linear regression analysis of twenty one terrestrial and aquatic environmental factors can partially explain (56%) the DOC concentration variation. In conclusion, this study highlights the complexity of the interactions among these environmental factors in determining DOC concentrations, thus calls for processes-based, non-linear methodologies to constrain uncertainties in riverine DOC cycling.« less</p> </li> <li> <p><a target="_blank" rel="noopener noreferrer" onclick="trackOutboundLink('http://adsabs.harvard.edu/abs/2015AGUFMGC12B..02C','NASAADS'); return false;" href="http://adsabs.harvard.edu/abs/2015AGUFMGC12B..02C"><span>Assessing and Synthesizing the Last Decade of Research on the Major Pools and Fluxes of the Carbon Cycle in the US and North America: An Interagency Governmental Perspective</span></a></p> <p><a target="_blank" rel="noopener noreferrer" href="http://adsabs.harvard.edu/abstract_service.html">NASA Astrophysics Data System (ADS)</a></p> <p>Cavallaro, N.; Shrestha, G.; Stover, D. B.; Zhu, Z.; Ombres, E. H.; Deangelo, B.</p> <p>2015-12-01</p> <p>The 2nd State of the Carbon Cycle Report (SOCCR-2) is focused on US and North American carbon stocks and fluxes in managed and unmanaged systems, including relevant carbon management science perspectives and tools for supporting and informing decisions. SOCCR-2 is inspired by the US Carbon Cycle Science Plan (2011) which emphasizes global scale research on long-lived, carbon-based greenhouse gases, carbon dioxide and methane, and the major pools and fluxes of the global carbon cycle. Accordingly, the questions framing the Plan inform this report's topical roadmap, with a focus on US and North America in the global context: 1) How have natural processes and human actions affected the global carbon cycle on land, in the atmosphere, in the oceans and in the ecosystem interfaces (e.g. coastal, wetlands, urban-rural)? 2) How have socio-economic trends affected the levels of the primary carbon-containing gases, carbon dioxide and methane, in the atmosphere? 3) How have species, ecosystems, natural resources and human systems been impacted by increasing greenhouse gas concentrations, the associated changes in climate, and by carbon management decisions and practices? To address these aspects, SOCCR-2 will encompass the following broad assessment framework: 1) Carbon Cycle at Scales (Global Perspective, North American Perspective, US Perspective, Regional Perspective); 2) Role of carbon in systems (Soils; Water, Oceans, Vegetation; Terrestrial-aquatic Interfaces); 3) Interactions/Disturbance/Impacts from/on the carbon cycle. 4) Carbon Management Science Perspective and Decision Support (measurements, observations and monitoring for research and policy relevant decision-support etc.). In this presentation, the Carbon Cycle Interagency Working Group and the U.S. Global Change Research Program's U.S. Carbon Cycle Science Program Office will highlight the scientific context, strategy, structure, team and production process of the report, which is part of the USGCRP's Sustained National Climate Assessment process.</p> </li> <li> <p><a target="_blank" rel="noopener noreferrer" onclick="trackOutboundLink('http://adsabs.harvard.edu/abs/2009AGUSM.B73C..03M','NASAADS'); return false;" href="http://adsabs.harvard.edu/abs/2009AGUSM.B73C..03M"><span>A New U.S. Carbon Cycle Science Plan</span></a></p> <p><a target="_blank" rel="noopener noreferrer" href="http://adsabs.harvard.edu/abstract_service.html">NASA Astrophysics Data System (ADS)</a></p> <p>Michalak, A. M.; Jackson, R.; Marland, G.; Sabine, C.</p> <p>2009-05-01</p> <p>The report "A U.S. carbon cycle science plan" (J. L. Sarmiento and S. C. Wofsy, U.S. Global Change Res. Program, Washington, D. C., 1999) outlined research priorities and promoted coordinated carbon cycle research across federal agencies in the United States for nearly a decade. Building on this framework and subsequent reports (http://www.carboncyclescience.gov/docs.php), a working group comprised of 27 scientists was formed in 2008 under the United States Carbon Cycle Science Program to review the 1999 Science Plan, and to develop an updated strategy for carbon cycle research for the period from 2010 to 2020. This comprehensive review is being conducted with wide input from the research and stakeholder communities. The recommendations of the Carbon Cycle Science Working Group (CCSWG) will go to U.S. agency managers who have collective responsibility for setting national carbon cycle science priorities and for sponsoring much of the carbon cycle research in the United States. This presentation will provide an update on the ongoing planning process, will outline the steps that the CCSWG is undertaking in building consensus towards an updated U.S. Carbon Cycle Science Plan, and will seek input on the best ways in which to coordinate efforts with ongoing and upcoming research in Canada and Mexico, as well as with ongoing work globally.</p> </li> <li> <p><a target="_blank" rel="noopener noreferrer" onclick="trackOutboundLink('http://adsabs.harvard.edu/abs/2016EGUGA..18.1221H','NASAADS'); return false;" href="http://adsabs.harvard.edu/abs/2016EGUGA..18.1221H"><span>Simulation of groundwater flow and evaluation of carbon sink in Lijiang Rivershed, China</span></a></p> <p><a target="_blank" rel="noopener noreferrer" href="http://adsabs.harvard.edu/abstract_service.html">NASA Astrophysics Data System (ADS)</a></p> <p>Hu, Bill X.; Cao, Jianhua; Tong, Juxiu; Gao, Bing</p> <p>2016-04-01</p> <p>It is important to study water and carbon cycle processes for water resource management, pollution prevention and global warming influence on southwest karst region of China. Lijiang river basin is selected as our study region. Interdisciplinary field and laboratory experiments with various technologies are conducted to characterize the karst aquifers in detail. Key processes in the karst water cycle and carbon cycle are determined. Based on the MODFLOW-CFP model, new watershed flow and carbon cycle models are developed coupled subsurface and surface water flow models, flow and chemical/biological models. Our study is focused on the karst springshed in Mao village. The mechanisms coupling carbon cycle and water cycle are explored. Parallel computing technology is used to construct the numerical model for the carbon cycle and water cycle in the small scale watershed, which are calibrated and verified by field observations. The developed coupling model for the small scale watershed is extended to a large scale watershed considering the scale effect of model parameters and proper model structure simplification. The large scale watershed model is used to study water cycle and carbon cycle in Lijiang rivershed, and to calculate the carbon flux and carbon sinks in the Lijiang river basin. The study results provide scientific methods for water resources management and environmental protection in southwest karst region corresponding to global climate change. This study could provide basic theory and simulation method for geological carbon sequestration in China karst region.</p> </li> <li> <p><a target="_blank" rel="noopener noreferrer" onclick="trackOutboundLink('https://www.osti.gov/servlets/purl/1172026','SCIGOV-STC'); return false;" href="https://www.osti.gov/servlets/purl/1172026"><span>Lightweight Materials for Automotive Application: An Assessment of Material Production Data for Magnesium and Carbon Fiber</span></a></p> <p><a target="_blank" rel="noopener noreferrer" href="http://www.osti.gov/search">DOE Office of Scientific and Technical Information (OSTI.GOV)</a></p> <p>Johnson, M. C.; Sullivan, J. L.</p> <p></p> <p>The use of lightweight materials in vehicle components, also known as “lightweighting,” can result in automobile weight reduction, which improves vehicle fuel economy and generally its environmental footprint. Materials often used for vehicle lightweighting include aluminum, magnesium, and polymers reinforced with either glass or carbon fiber. However, because alternative materials typically used for vehicle lightweighting require more energy to make on a per part basis than the material being replaced (often steel or iron), the fuel efficiency improvement induced by a weight reduction is partially offset by an increased energy for the vehicle material production. To adequately quantify this tradeoff,more » reliable and current values for life-cycle production energy are needed for both conventional and alternative materials. Our focus here is on the production of two such alternative materials: magnesium and carbon fibers. Both these materials are low density solids with good structural properties. These properties have enabled their use in applications where weight is an issue, not only for automobiles but also for aerospace applications. This report addresses the predominant production methods for these materials and includes a tabulation of available material and energy input data necessary to make them. The life cycle inventory (LCI) information presented herein represents a process chain analysis (PCA) approach to life cycle assessment (LCA) and is intended for evaluation as updated materials production data for magnesium and carbon fiber for inclusion into the Greenhouse gases, Regulated Emissions, and Energy use in Transportation model (GREET2_2012). The summary life-cycle metrics used to characterize the cradle-to-gate environmental performance of these materials are the cumulative energy demand (CED) and greenhouse gas emissions (GHG) per kilogram of material.« less</p> </li> <li> <p><a target="_blank" rel="noopener noreferrer" onclick="trackOutboundLink('http://adsabs.harvard.edu/abs/2014AGUFM.B23C0209M','NASAADS'); return false;" href="http://adsabs.harvard.edu/abs/2014AGUFM.B23C0209M"><span>Model evaluation using a community benchmarking system for land surface models</span></a></p> <p><a target="_blank" rel="noopener noreferrer" href="http://adsabs.harvard.edu/abstract_service.html">NASA Astrophysics Data System (ADS)</a></p> <p>Mu, M.; Hoffman, F. M.; Lawrence, D. M.; Riley, W. J.; Keppel-Aleks, G.; Kluzek, E. B.; Koven, C. D.; Randerson, J. T.</p> <p>2014-12-01</p> <p>Evaluation of atmosphere, ocean, sea ice, and land surface models is an important step in identifying deficiencies in Earth system models and developing improved estimates of future change. For the land surface and carbon cycle, the design of an open-source system has been an important objective of the International Land Model Benchmarking (ILAMB) project. Here we evaluated CMIP5 and CLM models using a benchmarking system that enables users to specify models, data sets, and scoring systems so that results can be tailored to specific model intercomparison projects. Our scoring system used information from four different aspects of global datasets, including climatological mean spatial patterns, seasonal cycle dynamics, interannual variability, and long-term trends. Variable-to-variable comparisons enable investigation of the mechanistic underpinnings of model behavior, and allow for some control of biases in model drivers. Graphics modules allow users to evaluate model performance at local, regional, and global scales. Use of modular structures makes it relatively easy for users to add new variables, diagnostic metrics, benchmarking datasets, or model simulations. Diagnostic results are automatically organized into HTML files, so users can conveniently share results with colleagues. We used this system to evaluate atmospheric carbon dioxide, burned area, global biomass and soil carbon stocks, net ecosystem exchange, gross primary production, ecosystem respiration, terrestrial water storage, evapotranspiration, and surface radiation from CMIP5 historical and ESM historical simulations. We found that the multi-model mean often performed better than many of the individual models for most variables. We plan to publicly release a stable version of the software during fall of 2014 that has land surface, carbon cycle, hydrology, radiation and energy cycle components.</p> </li> <li> <p><a target="_blank" rel="noopener noreferrer" onclick="trackOutboundLink('http://adsabs.harvard.edu/abs/2016AGUFMGC23K..02S','NASAADS'); return false;" href="http://adsabs.harvard.edu/abs/2016AGUFMGC23K..02S"><span>Institutional Context of Carbon Cycle Science Research in the U.S. and North America - A SOCCR perspective</span></a></p> <p><a target="_blank" rel="noopener noreferrer" href="http://adsabs.harvard.edu/abstract_service.html">NASA Astrophysics Data System (ADS)</a></p> <p>Shrestha, G.; Cavallaro, N.; Ste-Marie, C.</p> <p>2016-12-01</p> <p>Carbon cycle science has been a research priority in the U.S. for decades. Interagency coordination interests and research needs in U.S. carbon cycle science led to the establishment of the U.S. Carbon Cycle Science Program, the North American Carbon Program (NACP), the Ocean Carbon and Biogeochemistry Program (OCB) and other intergovernmental collaboration platforms such as CarboNA, involving the U.S., Mexico and Canada. This presentation highlights some of these activities, and the historical context, the institutional frameworks and the operational mechanisms that have helped to facilitate and advance large scale collaborative research in carbon cycle in the U.S. and North America.</p> </li> <li> <p><a target="_blank" rel="noopener noreferrer" onclick="trackOutboundLink('http://adsabs.harvard.edu/abs/2016GBioC..30.1682G','NASAADS'); return false;" href="http://adsabs.harvard.edu/abs/2016GBioC..30.1682G"><span>Anthropogenic carbon in the ocean—Surface to interior connections</span></a></p> <p><a target="_blank" rel="noopener noreferrer" href="http://adsabs.harvard.edu/abstract_service.html">NASA Astrophysics Data System (ADS)</a></p> <p>Groeskamp, Sjoerd; Lenton, Andrew; Matear, Richard; Sloyan, Bernadette M.; Langlais, Clothilde</p> <p>2016-11-01</p> <p>Quantifying the surface to interior transport of anthropogenic carbon (CA) is critical for projecting future carbon uptake and for improved understanding of the role of the oceans in the global carbon cycle. Here we develop and apply a diagnostic tool that provides a volumetric stream function in (CA,σ0) coordinates to calculate the total diapycnal CA transport in the ocean, where σ0 is the surface referenced potential density anomaly. We combine this with air-sea fluxes of CA to infer the internal ocean mixing of CA to obtain a closed globally integrated budget analyses of the ocean's CA transport. This diagnostic separates the contribution from the mean flow, seasonal cycles, trend, surface fluxes, and mixing in the distribution and the accumulation of CA in the ocean. We find that the redistribution of CA from the surface to the interior of the ocean is due to an interplay between circulation and mixing. The circulation component is dominated by the mean flow; however, effects due to seasonal cycles are significant for the CA redistribution. The two most important pathways for CA subduction are through the transformation of thermocline water (TW) into subantarctic mode water and by transformation of Circumpolar Deep Water (CDW) into lighter Antarctic Intermediate Water. The results suggest that an accurate representation of intermediate and mode water formation, deep water formation, and spatial and temporal distribution of ocean mixing in ocean models is essential to simulate and project the oceanic uptake of CA.</p> </li> <li> <p><a target="_blank" rel="noopener noreferrer" onclick="trackOutboundLink('http://adsabs.harvard.edu/abs/2017AGUFM.H51R..01Z','NASAADS'); return false;" href="http://adsabs.harvard.edu/abs/2017AGUFM.H51R..01Z"><span>A Time Series Analysis of Global Soil Moisture Data Products for Water Cycle Studies</span></a></p> <p><a target="_blank" rel="noopener noreferrer" href="http://adsabs.harvard.edu/abstract_service.html">NASA Astrophysics Data System (ADS)</a></p> <p>Zhan, X.; Yin, J.; Liu, J.; Fang, L.; Hain, C.; Ferraro, R. R.; Weng, F.</p> <p>2017-12-01</p> <p>Water is essential for sustaining life on our planet Earth and water cycle is one of the most important processes of out weather and climate system. As one of the major components of the water cycle, soil moisture impacts significantly the other water cycle components (e.g. evapotranspiration, runoff, etc) and the carbon cycle (e.g. plant/crop photosynthesis and respiration). Understanding of soil moisture status and dynamics is crucial for monitoring and predicting the weather, climate, hydrology and ecological processes. Satellite remote sensing has been used for soil moisture observation since the launch of the Scanning Multi-channel Microwave Radiometer (SMMR) on NASA's Nimbus-7 satellite in 1978. Many satellite soil moisture data products have been made available to the science communities and general public. The soil moisture operational product system (SMOPS) of NOAA NESDIS has been operationally providing global soil moisture data products from each of the currently available microwave satellite sensors and their blends. This presentation will provide an update of SMOPS products. The time series of each of these soil moisture data products are analyzed against other data products, such as precipitation and evapotranspiration from other independent data sources such as the North America Land Data Assimilation System (NLDAS). Temporal characteristics of these water cycle components are explored against some historical events, such as the 2010 Russian, 2010 China and 2012 United States droughts, 2015 South Carolina floods, etc. Finally whether a merged global soil moisture data product can be used as a climate data record is evaluated based on the above analyses.</p> </li> <li> <p><a target="_blank" rel="noopener noreferrer" onclick="trackOutboundLink('http://www.osti.gov/sciencecinema/biblio/1015174','SCIGOVIMAGE-SCICINEMA'); return false;" href="http://www.osti.gov/sciencecinema/biblio/1015174"><span>Combustion and Carbon Cycle 2.0 and Computation in CC 2.0 (Carbon Cycle 2.0)</span></a></p> <p><a target="_blank" rel="noopener noreferrer" href="http://www.osti.gov/sciencecinema/">ScienceCinema</a></p> <p>Cheng, Robert K.; Meza, Juan</p> <p>2018-05-04</p> <p>Robert Cheng and Juan Meza provide two presentations in one session at the Carbon Cycle 2.0 kick-off symposium Feb. 3, 2010. We emit more carbon into the atmosphere than natural processes are able to remove - an imbalance with negative consequences. Carbon Cycle 2.0 is a Berkeley Lab initiative to provide the science needed to restore this balance by integrating the Labs diverse research activities and delivering creative solutions toward a carbon-neutral energy future.</p> </li> <li> <p><a target="_blank" rel="noopener noreferrer" onclick="trackOutboundLink('http://www.osti.gov/sciencecinema/biblio/1015151','SCIGOVIMAGE-SCICINEMA'); return false;" href="http://www.osti.gov/sciencecinema/biblio/1015151"><span>A Call to Action: Carbon Cycle 2.0 (Carbon Cycle 2.0)</span></a></p> <p><a target="_blank" rel="noopener noreferrer" href="http://www.osti.gov/sciencecinema/">ScienceCinema</a></p> <p>Alivisatos, Paul [Lawrence Berkeley National Lab. (LBNL), Berkeley, CA (United States)</p> <p>2018-05-21</p> <p>Berkeley Lab Director Paul Alivisatos speaks at the Carbon Cycle 2.0 kick-off symposium Feb. 1, 2010. Humanity emits more carbon into the atmosphere than natural processes are able to remove - an imbalance with negative consequences.Carbon Cycle 2.0 is a Berkeley Lab initiative to provide the science needed to restore this balance by integrating the Labs diverse research activities and delivering creative solutions toward a carbon-neutral energy future. http://carboncycle2.lbl.gov/</p> </li> <li> <p><a target="_blank" rel="noopener noreferrer" onclick="trackOutboundLink('http://www.osti.gov/sciencecinema/biblio/1015158','SCIGOVIMAGE-SCICINEMA'); return false;" href="http://www.osti.gov/sciencecinema/biblio/1015158"><span>A Future with (out) Carbon Cycle 2.0 (Carbon Cycle 2.0)</span></a></p> <p><a target="_blank" rel="noopener noreferrer" href="http://www.osti.gov/sciencecinema/">ScienceCinema</a></p> <p>Collins, Bill [Lawrence Berkeley National Lab. (LBNL), Berkeley, CA (United States)</p> <p>2018-05-21</p> <p>Bill Collins, Head of LBNL's Climate Sciences Department, speaks at the Carbon Cycle 2.0 kick-off symposium Feb. 1, 2010. We emit more carbon into the atmosphere than natural processes are able to remove - an imbalance with negative consequences. Carbon Cycle 2.0 is a Berkeley Lab initiative to provide the science needed to restore this balance by integrating the Labs diverse research activities and delivering creative solutions toward a carbon-neutral energy future. http://carboncycle2.lbl.gov/</p> </li> <li> <p><a target="_blank" rel="noopener noreferrer" onclick="trackOutboundLink('http://adsabs.harvard.edu/abs/2015JPS...294..173N','NASAADS'); return false;" href="http://adsabs.harvard.edu/abs/2015JPS...294..173N"><span>Depth profiling the solid electrolyte interphase on lithium titanate (Li4Ti5O12) using synchrotron-based photoelectron spectroscopy</span></a></p> <p><a target="_blank" rel="noopener noreferrer" href="http://adsabs.harvard.edu/abstract_service.html">NASA Astrophysics Data System (ADS)</a></p> <p>Nordh, Tim; Younesi, Reza; Brandell, Daniel; Edström, Kristina</p> <p>2015-10-01</p> <p>The presence of a surface layer on lithium titanate (Li4Ti5O12, LTO) anodes, which has been a topic of debate in scientific literature, is here investigated with tunable high surface sensitive synchrotron-based photoelectron spectroscopy (PES) to obtain a reliable depth profile of the interphase. Li||LTO cells with electrolytes consisting of 1 M lithium hexafluorophosphate dissolved in ethylene carbonate:diethyl carbonate (LiPF6 in EC:DEC) were cycled in two different voltage windows of 1.0-2.0 V and 1.4-2.0 V. LTO electrodes were characterized after 5 and 100 cycles. Also the pristine electrode as such, and an electrode soaked in the electrolyte were analyzed by varying the photon energies enabling depth profiling of the outermost surface layer. The main components of the surface layer were found to be ethers, P-O containing compounds, and lithium fluoride.</p> </li> <li> <p><a target="_blank" rel="noopener noreferrer" onclick="trackOutboundLink('http://adsabs.harvard.edu/abs/2015AGUFM.V21B3037H','NASAADS'); return false;" href="http://adsabs.harvard.edu/abs/2015AGUFM.V21B3037H"><span>The Density and Compressibility of BaCO3-SrCO3-CaCO3-K2CO3-Na2CO3-Li2CO3 Liquids: New Measurements and a Systematic Trend with Cation Field Strength</span></a></p> <p><a target="_blank" rel="noopener noreferrer" href="http://adsabs.harvard.edu/abstract_service.html">NASA Astrophysics Data System (ADS)</a></p> <p>Hurt, S. M.; Lange, R. A.; Ai, Y.</p> <p>2015-12-01</p> <p>The volumetric properties of multi-component carbonate liquids are required to extend thermodynamic models that describe partial melting of the deep mantle (e.g. pMELTS; Ghiorso et al., 2003) to carbonate-bearing lithologies. Carbonate in the mantle is an important reservoir of carbon, which is released to the atmosphere as CO2 through volcanism, and thus contributes to the carbon cycle. Although MgCO3 is the most important carbonate component in the mantle, it is not possible to directly measure the 1-bar density and compressibility of MgCO3 liquid because, like other alkaline-earth carbonates, it decomposes at a temperature lower than its melting temperature. Despite this challenge, Liu and Lange (2003) and O'Leary et al. (2015) showed that the one bar molar volume, thermal expansion and compressibility of the CaCO3 liquid component could be obtained by measuring the density and sound speeds of stable liquids in the CaCO3-Li2CO3-Na2CO3-K2CO3 quaternary system at one bar. In this study, this same strategy is employed on SrCO3- and BaCO3-bearing alkali carbonate liquids. The density and sound speed of seven liquids in the SrCO3-Li2CO3-Na2CO3-K2CO3 quaternary and three liquids in the BaCO3-Li2CO3-Na2CO3-K2CO3 quaternary were measured from 739-1367K, with SrCO3 and BaCO3 concentrations ranging from 10-50 mol%. The density measurements were made using the double-bob Archimedean method and sound speeds were obtained with a frequency-sweep acoustic interferometer. The molar volume and sound speed measurements were used to calculate the isothermal compressibility of each liquid, and the results show the volumetric properties mix ideally with composition. The partial molar volume and compressibility of the SrCO3 and BaCO3 components are compared to those obtained for the CaCO3 component as a function of cation field strength. The results reveal a systematic trend that allows the partial molar volume and compressibility of the MgCO3 liquid component to be estimated.</p> </li> <li> <p><a target="_blank" rel="noopener noreferrer" onclick="trackOutboundLink('http://adsabs.harvard.edu/abs/2017E%26PSL.466..152T','NASAADS'); return false;" href="http://adsabs.harvard.edu/abs/2017E%26PSL.466..152T"><span>Sources and mobility of carbonate melts beneath cratons, with implications for deep carbon cycling, metasomatism and rift initiation</span></a></p> <p><a target="_blank" rel="noopener noreferrer" href="http://adsabs.harvard.edu/abstract_service.html">NASA Astrophysics Data System (ADS)</a></p> <p>Tappe, Sebastian; Romer, Rolf L.; Stracke, Andreas; Steenfelt, Agnete; Smart, Katie A.; Muehlenbachs, Karlis; Torsvik, Trond H.</p> <p>2017-05-01</p> <p>Kimberlite and carbonatite magmas that intrude cratonic lithosphere are among the deepest probes of the terrestrial carbon cycle. Their co-existence on thick continental shields is commonly attributed to continuous partial melting sequences of carbonated peridotite at >150 km depths, possibly as deep as the mantle transition zone. At Tikiusaaq on the North Atlantic craton in West Greenland, approximately 160 Ma old ultrafresh kimberlite dykes and carbonatite sheets provide a rare opportunity to study the origin and evolution of carbonate-rich melts beneath cratons. Although their Sr-Nd-Hf-Pb-Li isotopic compositions suggest a common convecting upper mantle source that includes depleted and recycled oceanic crust components (e.g., negative ΔεHf coupled with > + 5 ‰ δ7Li), incompatible trace element modelling identifies only the kimberlites as near-primary low-degree partial melts (0.05-3%) of carbonated peridotite. In contrast, the trace element systematics of the carbonatites are difficult to reproduce by partial melting of carbonated peridotite, and the heavy carbon isotopic signatures (-3.6 to - 2.4 ‰ δ13C for carbonatites versus -5.7 to - 3.6 ‰ δ13C for kimberlites) require open-system fractionation at magmatic temperatures. Given that the oxidation state of Earth's mantle at >150 km depth is too reduced to enable larger volumes of 'pure' carbonate melt to migrate, it is reasonable to speculate that percolating near-solidus melts of carbonated peridotite must be silicate-dominated with only dilute carbonate contents, similar to the Tikiusaaq kimberlite compositions (e.g., 16-33 wt.% SiO2). This concept is supported by our findings from the North Atlantic craton where kimberlite and other deeply derived carbonated silicate melts, such as aillikites, exsolve their carbonate components within the shallow lithosphere en route to the Earth's surface, thereby producing carbonatite magmas. The relative abundances of trace elements of such highly differentiated 'cratonic carbonatites' have only little in common with those of metasomatic agents that act on the deeper lithosphere. Consequently, carbonatite trace element systematics should only be used with caution when constraining carbon mobility and metasomatism at mantle depths. Regardless of the exact nature of carbonate-bearing melts within the mantle lithosphere, they play an important role in enrichment processes, thereby decreasing the stability of buoyant cratons and promoting rift initiation - as exemplified by the Mesozoic-Cenozoic breakup of the North Atlantic craton.</p> </li> <li> <p><a target="_blank" rel="noopener noreferrer" onclick="trackOutboundLink('https://pubs.er.usgs.gov/publication/70026713','USGSPUBS'); return false;" href="https://pubs.er.usgs.gov/publication/70026713"><span>Geochemical cycles in sediments deposited on the slopes of the Guaymas and Carmen Basins of the Gulf of California over the last 180 years</span></a></p> <p><a target="_blank" rel="noopener noreferrer" href="http://pubs.er.usgs.gov/pubs/index.jsp?view=adv">USGS Publications Warehouse</a></p> <p>Dean, W.; Pride, C.; Thunell, R.</p> <p>2004-01-01</p> <p>Sediments deposited on the slopes of the Guaymas and Carmen Basins in the central Gulf of California were recovered in two box cores. Q-mode factor analyses identified detrital-clastic, carbonate, and redox associations in the elemental composition of these sediments. The detrital-clastic fraction appears to contain two source components, a more mafic component presumably derived from the Sierra Madre Occidental along the west coast of Mexico, and a more felsic component most likely derived from sedimentary rocks (mostly sandstones) of the Colorado Plateau and delivered by the Colorado River. The sediments also contain significant siliceous biogenic components and minor calcareous biogenic components, but those components were not quantified in this study. Redox associations were identified in both cores based on relatively high concentrations of molybdenum, which is indicative of deposition under conditions of sulfate reduction. Decreases in concentrations of molybdenum in younger sediments suggest that the bottom waters of the Gulf have became more oxygenated over the last 100 years. Many geochemical components in both box cores exhibit distinct cyclicity with periodicities of 10-20 years. The most striking are 20-year cycles in the more mafic components (e.g., titanium), particularly in sediments deposited during the 19th century. In that century, the titanium cycles are in very good agreement with warm phases of the Pacific Decadal Oscillation, implying that at times of greater influx of titanium-rich volcanic debris, there were more El Nin??os and higher winter precipitation. The cycles are interpreted as due to greater and lesser riverine influx of volcanic rock debris from the Sierra Madre. There is also spectral evidence for periodicities of 4-8 and 8-16 years, suggesting that the delivery of detrital-clastic material is responding to some multiannual (ENSO?) forcing.</p> </li> </ol> <div class="pull-right"> <ul class="pagination"> <li><a href="#" onclick='return showDiv("page_1");'>«</a></li> <li><a href="#" onclick='return showDiv("page_12");'>12</a></li> <li><a href="#" onclick='return showDiv("page_13");'>13</a></li> <li class="active"><span>14</span></li> <li><a href="#" onclick='return showDiv("page_15");'>15</a></li> <li><a href="#" onclick='return showDiv("page_16");'>16</a></li> <li><a href="#" onclick='return showDiv("page_25");'>»</a></li> </ul> </div> </div><!-- col-sm-12 --> </div><!-- row --> </div><!-- page_14 --> <div id="page_15" class="hiddenDiv"> <div class="row"> <div class="col-sm-12"> <div class="pull-right"> <ul class="pagination"> <li><a href="#" onclick='return showDiv("page_1");'>«</a></li> <li><a href="#" onclick='return showDiv("page_13");'>13</a></li> <li><a href="#" onclick='return showDiv("page_14");'>14</a></li> <li class="active"><span>15</span></li> <li><a href="#" onclick='return showDiv("page_16");'>16</a></li> <li><a href="#" onclick='return showDiv("page_17");'>17</a></li> <li><a href="#" onclick='return showDiv("page_25");'>»</a></li> </ul> </div> </div> </div> <div class="row"> <div class="col-sm-12"> <ol class="result-class" start="281"> <li> <p><a target="_blank" rel="noopener noreferrer" onclick="trackOutboundLink('http://adsabs.harvard.edu/abs/2010EGUGA..1213677S','NASAADS'); return false;" href="http://adsabs.harvard.edu/abs/2010EGUGA..1213677S"><span>The joint Russia-US-Sweden studies in the East-Siberian Arctic Shelf (ESAS) during the last decade (1999-2009): an overview</span></a></p> <p><a target="_blank" rel="noopener noreferrer" href="http://adsabs.harvard.edu/abstract_service.html">NASA Astrophysics Data System (ADS)</a></p> <p>Sergienko, Valentin; Shakhova, Natalia; Dudarev, Oleg; Gustafsson, Orjan; Anderson, Leif; Semiletov, Igor</p> <p>2010-05-01</p> <p>The Arctic Ocean is surrounded by permafrost, which is being degraded at an increasing rate under conditions of warming which are most pronounced in Siberia and Alaska . A major constraint on our ability to understand linkages between the Arctic Ocean and the global climate system is the scarcity of observational data in the Siberian Arctic marginal seas where major fresh water input and terrestrial CNP fluxes exist. The East-Siberian Sea has never been investigated by modern techniques despite the progress that has been made in new technologies useful for measuring ocean characteristics of interest. In this multi-year international project which joins scientists from 3 nations (Russia-USA-Sweden), and in cooperation with scientists from other countries (UK, Netherlands) we focus on he ESAS which is poorly explored areas located west from the U.S.-Russia boundary. In this report we overview the main field activities and present some results obtained during the last decade (1999-2009). Siberian freshwater discharge to the Arctic Ocean is expected to increase with increasing temperatures, potentially resulting in greater river export of old terrigenous organic carbon to the ocean. We suggest that rivers integrate variability in the components of the hydrometeorological regime, including soil condition, permafrost seasonal thaw, and thermokarst development, all the variables that determine atmospheric and ground water supply for the rivers and chemical weathering in their watershed.. It has been found that 1) carbon dioxide and methane fluxes are significant (and non-counted) components of the carbon cycling in the Arctic Ocean; 2) transport of eroded terrestrial material plays a major role in the accumulation of carbon in the ESAS (Dudarev et al., Gustafsson et al., Vonk et al., Sanchez-Garcia et al., Charkin et al., Semiletov et al., this session) ; 3) the seabed is a major CH4 source over the ESAS (N.Shakhova et al., this session); 3) eroded carbon is biodegradable (all reports, this session); 4) oxidation of eroded carbon onshore and offshore is a strong source of carbon dioxide (Piko et al. and Semiletov et al., this session). Thus studying carbon cycling in the East Siberian Arctic marginal seas has a high scientific priority in order to establish the carbon budget and evaluate the role of the Arctic region in global carbon cycling, especially in the coastal zone where the redistribution of carbon between terrestrial and marine environments occurs and the characteristics of carbon exchange with atmosphere are unknown. Initial scientific plan for the next decade is discussed. This study was supported by the Russian Foundation for Basic Research (since 1994), International (Soros) Scientific Foundation, ISF (1994-1995), Russian Government and ISF (1995), McArthur Foundation (2000-2001), FEBRAS/RAS (since 2003), IARC (since 2001), NSF (since 2003), NOAA (since 2005), SU (since 2007), and Wallenberg Foundation (since 2008).</p> </li> <li> <p><a target="_blank" rel="noopener noreferrer" onclick="trackOutboundLink('http://adsabs.harvard.edu/abs/2016EGUGA..18.9143Z','NASAADS'); return false;" href="http://adsabs.harvard.edu/abs/2016EGUGA..18.9143Z"><span>The impact of extreme environmental factors on the mineralization potential of the soil</span></a></p> <p><a target="_blank" rel="noopener noreferrer" href="http://adsabs.harvard.edu/abstract_service.html">NASA Astrophysics Data System (ADS)</a></p> <p>Zinyakova, Natalia; Semenov, Vyacheslav</p> <p>2016-04-01</p> <p>Warming, drying, wetting are the prevalent disturbing natural impacts that affect the upper layers of uncultivated and arable soils. The effect of drying-wetting cycles act as a physiological stress for the soil microbial community and cause changes in its structure, the partial death or lysis of the microbial biomass. The mobilization of the SOM and the stabilization of the potentially mineralizable components lead to change of mineralization potential in the soil. To test the effects of different moisture regime on plant growth and soil biological properties, plot experiment with the gray forest soil including trials with plants (corn) and bare fallow was performed. Different regimes of soil moisture (conditionally optimal, relatively deficient soil moisture and repeated cycles of drying-wetting) were created. Control of soil moisture was taken every two or three days. Gas sampling was carried out using closed chambers. Soil samples were collected at the end of the pot experiment. The potentially mineralizable content of soil organic carbon (SOC) was measured by biokinetic method based on (1) aerobic incubation of soil samples under constant temperature and moisture conditions during 158 days, (2) quantitation of C-CO2, and (3) fitting of C-CO2 cumulative curve by a model of first-order kinetic. Total soil organic carbon was measured by Tyrin's wet chemical oxidation method. Permanent deficient moisture in the soil favored the preservation of potentially mineralizable SOC. Two repeated cycles of drying-wetting did not reduce the potentially mineralizable carbon content in comparison with control under optimal soil moisture during 90 days of experiment. The emission loss of C-CO2 from the soil with plants was 1.4-1.7 times higher than the decrease of potentially mineralizable SOC due to the contribution of root respiration. On the contrary, the decrease of potentially mineralized SOC in the soil without plants was 1.1-1.2 times larger than C-CO2 emissions from the soil as a result of stabilization processes. Thus, the alternation of drying-wetting cycles results in 1) the death of microbial biomass and recolonization of the soil microorganisms; 2) favors the splitting and degradation of soil aggregates, as well as the reaggregation and stabilization of aggregates; 3) contributes to the mobilization of the SOM and also 4) initiates the stabilization of the potentially mineralizable components. The effect of drying-wetting cycles is expressed not so much in the loss of the total soil organic carbon as in the degradation of the SOM quality with decreasing its mineralization potential. We can conclude that different soil moisture regimes lead to essential changes of mineralization potential in the gray forest soil. The amount of mineralization loss soil carbon via C-CO2 emission is directly associated with the decrease of potentially mineralizable carbon. Deficient moisture is a reason for temporarily sequestration of SOC potentially mineralizable under optimal moisture. This work was supported by RSF. Project number 14-14-00625</p> </li> <li> <p><a target="_blank" rel="noopener noreferrer" onclick="trackOutboundLink('https://www.ncbi.nlm.nih.gov/pubmed/25068887','PUBMED'); return false;" href="https://www.ncbi.nlm.nih.gov/pubmed/25068887"><span>Stretchable carbon nanotube/ion-gel supercapacitors with high durability realized through interfacial microroughness.</span></a></p> <p><a target="_blank" rel="noopener noreferrer" href="https://www.ncbi.nlm.nih.gov/entrez/query.fcgi?DB=pubmed">PubMed</a></p> <p>Lee, Jiho; Kim, Wonbin; Kim, Woong</p> <p>2014-08-27</p> <p>A critical problem with stretchable supercapacitors developed to date has been evaporation of a volatile component of their electrolyte, causing failure. In this work, we demonstrated successful use of an ionic-liquid-based nonvolatile gel (ion-gel) electrolyte in carbon nanotube (CNT)-based stretchable supercapacitors. The CNT/ion-gel supercapacitors showed high capacitance retention (96.6%) over 3000 stretch cycles at 20% strain. The high durability against stretch cycles was achieved by introducing microroughness at the interfaces between different materials. The microroughness was produced by the simple process of imprinting the surface microstructure of office paper onto a poly(dimethylsiloxane) substrate; the surface texture is reproduced in successive current collector and CNT layers. Adhesion between the different layers was strengthened by this roughness and prevented delamination over repeated stretch cycles. The addition of a CNT layer decreased the sensitivity of electrical characteristics to stretching. Moreover, the ion-gel increases the operating voltage window (3 V) and hence the energy density. We believe our demonstration will greatly contribute to the development of flexible and/or stretchable energy-storage devices with high durability.</p> </li> <li> <p><a target="_blank" rel="noopener noreferrer" onclick="trackOutboundLink('http://adsabs.harvard.edu/abs/2017Nanot..28Q5204H','NASAADS'); return false;" href="http://adsabs.harvard.edu/abs/2017Nanot..28Q5204H"><span>A facile one-step approach for the fabrication of polypyrrole nanowire/carbon fiber hybrid electrodes for flexible high performance solid-state supercapacitors</span></a></p> <p><a target="_blank" rel="noopener noreferrer" href="http://adsabs.harvard.edu/abstract_service.html">NASA Astrophysics Data System (ADS)</a></p> <p>Huang, Sanqing; Han, Yichuan; Lyu, Siwei; Lin, Wenzhen; Chen, Peishan; Fang, Shaoli</p> <p>2017-10-01</p> <p>Wearable electronics are in high demand, requiring that all the components are flexible. Here we report a facile approach for the fabrication of flexible polypyrrole nanowire (NPPy)/carbon fiber (CF) hybrid electrodes with high electrochemical activity using a low-cost, one-step electrodeposition method. The structure of the NPPy/CF electrodes can be easily controlled by the applied electrical potential and electrodeposition time. Our NPPy/CF-based electrodes showed high flexibility, conductivity, and stability, making them ideal for flexible all-solid-state fiber supercapacitors. The resulting NPPy/CF-based supercapacitors provided a high specific capacitance of 148.4 F g-1 at 0.128 A g-1, which is much higher than for supercapacitors based on polypyrrole film/CF (38.3 F g-1) and pure CF (0.6 F g-1) under the same conditions. The NPPy/CF-based supercapacitors also showed high bending and cycling stability, retaining 84% of the initial capacitance after 500 bending cycles, and 91% of the initial capacitance after 5000 charge/discharge cycles.</p> </li> <li> <p><a target="_blank" rel="noopener noreferrer" onclick="trackOutboundLink('https://www.ncbi.nlm.nih.gov/pubmed/28786401','PUBMED'); return false;" href="https://www.ncbi.nlm.nih.gov/pubmed/28786401"><span>A facile one-step approach for the fabrication of polypyrrole nanowire/carbon fiber hybrid electrodes for flexible high performance solid-state supercapacitors.</span></a></p> <p><a target="_blank" rel="noopener noreferrer" href="https://www.ncbi.nlm.nih.gov/entrez/query.fcgi?DB=pubmed">PubMed</a></p> <p>Huang, Sanqing; Han, Yichuan; Lyu, Siwei; Lin, Wenzhen; Chen, Peishan; Fang, Shaoli</p> <p>2017-10-27</p> <p>Wearable electronics are in high demand, requiring that all the components are flexible. Here we report a facile approach for the fabrication of flexible polypyrrole nanowire (NPPy)/carbon fiber (CF) hybrid electrodes with high electrochemical activity using a low-cost, one-step electrodeposition method. The structure of the NPPy/CF electrodes can be easily controlled by the applied electrical potential and electrodeposition time. Our NPPy/CF-based electrodes showed high flexibility, conductivity, and stability, making them ideal for flexible all-solid-state fiber supercapacitors. The resulting NPPy/CF-based supercapacitors provided a high specific capacitance of 148.4 F g -1 at 0.128 A g -1 , which is much higher than for supercapacitors based on polypyrrole film/CF (38.3 F g -1 ) and pure CF (0.6 F g -1 ) under the same conditions. The NPPy/CF-based supercapacitors also showed high bending and cycling stability, retaining 84% of the initial capacitance after 500 bending cycles, and 91% of the initial capacitance after 5000 charge/discharge cycles.</p> </li> <li> <p><a target="_blank" rel="noopener noreferrer" onclick="trackOutboundLink('https://www.pubmedcentral.nih.gov/articlerender.fcgi?tool=pmcentrez&artid=183030','PMC'); return false;" href="https://www.pubmedcentral.nih.gov/articlerender.fcgi?tool=pmcentrez&artid=183030"><span>Biochemical Composition of Dissolved Organic Carbon Derived from Phytoplankton and Used by Heterotrophic Bacteria</span></a></p> <p><a target="_blank" rel="noopener noreferrer" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?DB=pmc">PubMed Central</a></p> <p>Sundh, Ingvar</p> <p>1992-01-01</p> <p>The molecular size distribution and biochemical composition of the dissolved organic carbon released from natural communities of lake phytoplankton (photosynthetically produced dissolved organic carbon [PDOC]) and subsequently used by heterotrophic bacteria were determined in three lakes differing in trophic status and concentration of humic substances. After incubation of epilimnetic lake water samples with H14CO3- over one diel cycle, the phytoplankton were removed by size-selective filtration. The filtrates, still containing most of the heterotrophic bacteria, were reincubated in darkness (heterotrophic incubation). Differences in the amount and composition of PDO14C between samples collected before the heterotrophic incubation and samples collected afterwards were considered to be a result of bacterial utilization. The PDO14C collected at the start of the heterotrophic incubations always contained both high (>10,000)- and low (<1,000)-molecular-weight (MW) components and sometimes contained intermediate-MW components as well. In general, bacterial turnover rates of the low-MW components were fairly rapid, whereas the high-MW components were utilized slowly or not at all. In the humic lake, the intermediate-MW components accounted for a large proportion of the net PDO14C and were subject to rapid bacterial utilization. This fraction probably consisted almost entirely of polysaccharides of ca. 6,000 MW. Amino acids and peptides, other organic acids, and carbohydrates could all be quantitatively important parts of the low-MW PDO14C that was utilized by the heterotrophic bacteria, but the relative contributions of these fractions differed widely. It was concluded that, generally, low-MW components of PDOC are quantitatively much more important to the bacteria than are high-MW components, that PDOC released from phytoplankton does not contain substances of quantitative importance as bacterial substrates in all situations, and that high-MW components of PDOC probably contribute to the buildup of refractory, high-MW dissolved organic carbon in pelagic environments. PMID:16348767</p> </li> <li> <p><a target="_blank" rel="noopener noreferrer" onclick="trackOutboundLink('https://www.ncbi.nlm.nih.gov/pubmed/27760851','PUBMED'); return false;" href="https://www.ncbi.nlm.nih.gov/pubmed/27760851"><span>Carbon utilization profile of the filamentous fungal species Fusarium fujikuroi, Penicillium decumbens, and Sarocladium strictum isolated from marine coastal environments.</span></a></p> <p><a target="_blank" rel="noopener noreferrer" href="https://www.ncbi.nlm.nih.gov/entrez/query.fcgi?DB=pubmed">PubMed</a></p> <p>Fuentes, Marcelo E; Quiñones, Renato A</p> <p></p> <p>Facultative marine filamentous fungi have recently emerged as a functional component in coastal marine systems. However, little is known about their ecological role and functions in biogeochemical cycles. Penicillium decumbens, S. strictum, and F. fujikuroi were isolated from the coastal upwelling zone off south-central Chile. Their carbon profiles were characterized using Biolog FF MicroPlates. These species used a wide range of carbon sources, mainly carbohydrates, but also amino acids, suggesting the use of metabolic routes that include glycolysis/gluconeogenesis. Substrate richness revealed a great capacity for the utilization of nutritional sources, reflected by the following Shannon Indices of utilization of specific substrates: 4.02 for S. strictum, 4.01 for P. decumbes, and 3.91 for F. fujikuroi, which reveals a high physiological capacity for oxidizing different substrates. Significant differences were found between 18 substrates utilized by all three species. Results suggest that filamentous fungi should be considered an integral part of the marine microbial community and included in biogeochemical cycling models of upwelling ecosystems.</p> </li> <li> <p><a target="_blank" rel="noopener noreferrer" onclick="trackOutboundLink('http://adsabs.harvard.edu/abs/2017ApSS..423..210S','NASAADS'); return false;" href="http://adsabs.harvard.edu/abs/2017ApSS..423..210S"><span>High-performance supercapacitors using flexible and freestanding MnOx/carbamide carbon nanofibers</span></a></p> <p><a target="_blank" rel="noopener noreferrer" href="http://adsabs.harvard.edu/abstract_service.html">NASA Astrophysics Data System (ADS)</a></p> <p>Samuel, Edmund; Jo, Hong Seok; Joshi, Bhavana; Park, Hyun Goo; Kim, Yong Il; An, Seongpil; Swihart, Mark T.; Yun, Je Moon; Kim, Kwang Ho; Yoon, Sam S.</p> <p>2017-11-01</p> <p>We demonstrate the fabrication of a MnOx/carbamide carbon nanofiber (CCNF) composite consisting of MnO particles embedded in CCNFs as a highly flexible and freestanding electrode material for supercapacitors. A sacrificial polymer component, polymethylmethacrylate, included in the precursor solution, pyrolyzes during heating, resulting in pores in the fibers, some of which are filled by the MnO nanocrystals. Carbamide is added to control the size of the MnOx particles as well as to increase the carbon content of the composite and hence its conductivity. The X-ray diffraction and Raman spectra of the composite show that the MnO particles formed have low crystallinity. Transmission electron microscopy confirms that the MnO particles are distributed very uniformly over the CCNFs. Symmetric supercapacitors constructed using electrodes of this composite exhibit specific capacitances of 498 F•g-1 at a scan rate of 10 mV•s-1 and 271 F•g-1 at a current density of 1 A•g-1. They also exhibit excellent long-term cycling performance, retaining 93% of their initial capacity after 5000 cycles of galvanostatic charging/discharging.</p> </li> <li> <p><a target="_blank" rel="noopener noreferrer" onclick="trackOutboundLink('https://www.osti.gov/pages/biblio/1261436-optimal-stomatal-behaviour-around-world','SCIGOV-DOEP'); return false;" href="https://www.osti.gov/pages/biblio/1261436-optimal-stomatal-behaviour-around-world"><span>Optimal stomatal behaviour around the world</span></a></p> <p><a target="_blank" rel="noopener noreferrer" href="http://www.osti.gov/pages">DOE PAGES</a></p> <p>Lin, Yan-Shih; Medlyn, Belinda E.; Duursma, Remko A.; ...</p> <p>2015-03-02</p> <p>Stomatal conductance (g s) is a key land-surface attribute as it links transpiration, the dominant component of global land evapotranspiration, and photosynthesis, the driving force of the global carbon cycle. Despite the pivotal role of g s in predictions of global water and carbon cycle changes, a global-scale database and an associated globally applicable model of g s that allow predictions of stomatal behaviour are lacking. Here, we present a database of globally distributed g s obtained in the field for a wide range of plant functional types (PFTs) and biomes. We find that stomatal behaviour differs among PFTs accordingmore » to their marginal carbon cost of water use, as predicted by the theory underpinning the optimal stomatal model 1 and the leaf and wood economics spectrum 2,3. We also demonstrate a global relationship with climate. In conclusion, these findings provide a robust theoretical framework for understanding and predicting the behaviour of g s across biomes and across PFTs that can be applied to regional, continental and global-scale modelling of ecosystem productivity, energy balance and ecohydrological processes in a future changing climate.« less</p> </li> <li> <p><a target="_blank" rel="noopener noreferrer" onclick="trackOutboundLink('http://adsabs.harvard.edu/abs/2017AGUFM.H21M..01G','NASAADS'); return false;" href="http://adsabs.harvard.edu/abs/2017AGUFM.H21M..01G"><span>Coupling between the continental carbon and water cycles</span></a></p> <p><a target="_blank" rel="noopener noreferrer" href="http://adsabs.harvard.edu/abstract_service.html">NASA Astrophysics Data System (ADS)</a></p> <p>Gentine, P.; Lemordant, L. A.; Green, J. K.</p> <p>2017-12-01</p> <p>The continental carbon adn water cycles are fundamentally coupled through leaf gas exchange at the stomata level. IN this presnetation we will emphasize the importance of this coupling for the future of the water cycle (runoff, evaporation, soil moisture) and in turn the implications for the carbon cycle and the capacity of continents to act as a carbon dioxyde sink in the future. Opprtunites from coupled carbon-water monitoring platforms will be then emphasized.</p> </li> <li> <p><a target="_blank" rel="noopener noreferrer" onclick="trackOutboundLink('http://adsabs.harvard.edu/abs/2009AGUFM.B53C0402W','NASAADS'); return false;" href="http://adsabs.harvard.edu/abs/2009AGUFM.B53C0402W"><span>The Borden Micrometeorological Experiment 2009 (BMW09): Micrometeorology and Stable Isotopes for Carbon Cycle Studies</span></a></p> <p><a target="_blank" rel="noopener noreferrer" href="http://adsabs.harvard.edu/abstract_service.html">NASA Astrophysics Data System (ADS)</a></p> <p>Warland, J. S.; Wagner-Riddle, C.; Staebler, R. M.; Lee, X.; Bartlett, P. A.; Brown, S. E.; Kim, K.; Santos, E. A.; Chang, K.</p> <p>2009-12-01</p> <p>A large collaborative experiment took place during summer 2009 at the Environment Canada tower site on CFB Borden in southern Ontario. The site is a long-term flux monitoring station, instrumented for eddy covariance measurements of CO2 and H2O, soil respiration, canopy profiles of CO2, H2O and temperature, net radiation, and standard meteorological variables. During BMW09, we brought to the site additional instrumentation to monitor gradients of stable isotopes of CO2 and H2O, turbulence profiles in the canopy and additional soil respiration data. Tunable diode laser trace gas analyzers were used to make continuous, high-frequency measurements of 12CO2, 13CO2 and C16O18O and H216O, HDO and H218O. Measurements were made of gradients of these isotopes above the canopy and in the understory. Profiles of CO2, H2O, temperature and turbulence statistics were measured for inverse Lagrangian analysis, where concentration profiles are used to determine source strength profiles through the canopy, thus separating soil, understory and overstory components of the net exchange made by eddy covariance. The project combines stable isotope measurements with novel micrometeorological techniques with the goal of developing improved operational measurements and gaining new insight into carbon and water cycles through this two-pronged approach. The overall goal of this intensive measurement campaign was to provide detailed data on the carbon and water cycles within this natural ecosystem for use in model testing and improvement. Specifically, the project will use this data with the C&N-CLASS model (the Canadian Land Surface Scheme with additional carbon and nitrogen routines) to improve its ability to predict changes to natural ecosystems under a changing climate when used within GCM simulations. This poster will present an overview of the project, highlight preliminary results, and illustrate how these disparate datasets will be tied together to provide new insight into carbon cycling.</p> </li> <li> <p><a target="_blank" rel="noopener noreferrer" onclick="trackOutboundLink('https://ntrs.nasa.gov/search.jsp?R=19930068547&hterms=Tuskegee&qs=Ntx%3Dmode%2Bmatchall%26Ntk%3DAll%26N%3D0%26No%3D90%26Ntt%3DTuskegee','NASA-TRS'); return false;" href="https://ntrs.nasa.gov/search.jsp?R=19930068547&hterms=Tuskegee&qs=Ntx%3Dmode%2Bmatchall%26Ntk%3DAll%26N%3D0%26No%3D90%26Ntt%3DTuskegee"><span>Effect of mission cycling on the fatigue performance of SiC-coated carbon-carbon composites</span></a></p> <p><a target="_blank" rel="noopener noreferrer" href="http://ntrs.nasa.gov/search.jsp">NASA Technical Reports Server (NTRS)</a></p> <p>Mahfuz, H.; Das, P. S.; Jeelani, S.; Baker, D. M.; Johnson, S. A.</p> <p>1993-01-01</p> <p>The effects of thermal and pressure cycling on the fatigue performance of carbon-carbon composites, and the influence of mission cycling on these effects, were investigated by subjecting both virgin and mission-cycled two-dimensional specimens of SiC-coated carbon-carbon composites to fatigue tests, conducted at room temperature in three-point bending, with a stress ratio of 0.2 and a frequency of 1 Hz. It was found that the fatigue strength of C-C composites is high (about 90 percent of the ultimate flexural strength), but decreased with the mission cycling. The lowering of the fatigue strength with mission cycling is attributed to the increase in interfacial bond strength due to thermal and pressure cycling of the material. The already high sensitivity of C-C composites to stress during cyclic loading increases further with the amount of mission cycling. Results of NDE suggest that the damage growth in virgin C-C, in the high-cycle range, is slow at the initial stage of the cyclic life, but propagates rapidly after certain threshold cycles of the fatigue life.</p> </li> <li> <p><a target="_blank" rel="noopener noreferrer" onclick="trackOutboundLink('http://adsabs.harvard.edu/abs/2014AGUFMPP54B..05R','NASAADS'); return false;" href="http://adsabs.harvard.edu/abs/2014AGUFMPP54B..05R"><span>Insights into Paleogene biogeochemistry from coupled carbon and sulfur isotopes in foraminiferal calcite.</span></a></p> <p><a target="_blank" rel="noopener noreferrer" href="http://adsabs.harvard.edu/abstract_service.html">NASA Astrophysics Data System (ADS)</a></p> <p>Rennie, V.; Paris, G.; Abramovitch, S.; Sessions, A. L.; Adkins, J. F.; Turchyn, A. V.</p> <p>2014-12-01</p> <p>The Paleogene witnessed large-scale environmental changes, including the beginning of long-term Cenozoic cooling. The carbon isotope composition of foraminiferal calcite suggests a major reorganization of the carbon cycle over the Paleogene, with enhanced organic carbon burial in the Paleocene, and subsequent oxidation of this organic carbon or increased volcanism throughout the Eocene. The sulfur cycle is linked to the carbon cycle via the breakdown of organic carbon during bacterial sulfate reduction. Over geological time, carbon and sulfur isotopic shifts are often coupled due to enhanced pyrite burial being coupled to enhanced organic carbon burial, and enhanced pyrite weathering being coupled to enhanced organic carbon weathering. However, over the Paleogene, carbon and sulfur isotopes are fully decoupled, with the sulfur isotope record showing only one major shift in the early Eocene, after most of the carbon isotope variability is complete. One complication of interpreting the evolution of the sulfur cycle over the Cenozoic, is the fact that the mineral proxies used (typically barite) may not be temporally coincident with those used to reconstruct the carbon cycle (typically carbonate). Furthermore, these minerals are preserved in different locations, and therefore often must be extracted from different sediment cores in different ocean basins, leading to age-model uncertainty when the records are merged. To properly ascertain the phasing between early Cenozoic changes in the carbon cycle and the sulfur cycle, we would ideally measure all isotope records on the same mineral. A new sulfur isotope analytical technique [1] has been optimised for foraminiferal calcite as a proxy for seawater δ34SSO4. The δ34SSO4 in foraminiferal calcite can then be tied to records of carbon isotopes from stratigraphically identical samples, resolving previous age model uncertainties. We present coupled carbon and sulfur isotope records from the same core over the early-to-mid Eocene, to better resolve the relative timing of changes in the carbon and sulfur cycles. We use a numerical model to explore the environmental changes necessary for the observed evolution in both the carbon and sulfur cycles. [1] Paris et al, 2013 Chemical Geology, 345, 50-61</p> </li> <li> <p><a target="_blank" rel="noopener noreferrer" onclick="trackOutboundLink('http://adsabs.harvard.edu/abs/2009AGUFMED33A0544S','NASAADS'); return false;" href="http://adsabs.harvard.edu/abs/2009AGUFMED33A0544S"><span>The GLOBE Carbon Cycle Project: Using a systems approach to understand carbon and the Earth's climate system</span></a></p> <p><a target="_blank" rel="noopener noreferrer" href="http://adsabs.harvard.edu/abstract_service.html">NASA Astrophysics Data System (ADS)</a></p> <p>Silverberg, S. K.; Ollinger, S. V.; Martin, M. E.; Gengarelly, L. M.; Schloss, A. L.; Bourgeault, J. L.; Randolph, G.; Albrechtova, J.</p> <p>2009-12-01</p> <p>National Science Content Standards identify systems as an important unifying concept across the K-12 curriculum. While this standard exists, there is a recognized gap in the ability of students to use a systems thinking approach in their learning. In a similar vein, both popular media as well as some educational curricula move quickly through climate topics to carbon footprint analyses without ever addressing the nature of carbon or the carbon cycle. If students do not gain a concrete understanding of carbon’s role in climate and energy they will not be able to successfully tackle global problems and develop innovative solutions. By participating in the GLOBE Carbon Cycle project, students learn to use a systems thinking approach, while at the same time, gaining a foundation in the carbon cycle and it's relation to climate and energy. Here we present the GLOBE Carbon Cycle project and materials, which incorporate a diverse set of activities geared toward upper middle and high school students with a variety of learning styles. A global carbon cycle adventure story and game let students see the carbon cycle as a complete system, while introducing them to systems thinking concepts including reservoirs, fluxes and equilibrium. Classroom photosynthesis experiments and field measurements of schoolyard vegetation brings the global view to the local level. And the use of computer models at varying levels of complexity (effects on photosynthesis, biomass and carbon storage in global biomes, global carbon cycle) not only reinforces systems concepts and carbon content, but also introduces students to an important scientific tool necessary for understanding climate change.</p> </li> <li> <p><a target="_blank" rel="noopener noreferrer" onclick="trackOutboundLink('http://adsabs.harvard.edu/abs/2015AGUFM.H43D1523H','NASAADS'); return false;" href="http://adsabs.harvard.edu/abs/2015AGUFM.H43D1523H"><span>Karst medium characterization and simulation of groundwater flow in Lijiang Riversed, China</span></a></p> <p><a target="_blank" rel="noopener noreferrer" href="http://adsabs.harvard.edu/abstract_service.html">NASA Astrophysics Data System (ADS)</a></p> <p>Hu, B. X.</p> <p>2015-12-01</p> <p>It is important to study water and carbon cycle processes for water resource management, pollution prevention and global warming influence on southwest karst region of China. Lijiang river basin is selected as our study region. Interdisciplinary field and laboratory experiments with various technologies are conducted to characterize the karst aquifers in detail. Key processes in the karst water cycle and carbon cycle are determined. Based on the MODFLOW-CFP model, new watershed flow and carbon cycle models are developed coupled subsurface and surface water flow models, flow and chemical/biological models. Our study is focused on the karst springshed in Mao village. The mechanisms coupling carbon cycle and water cycle are explored. Parallel computing technology is used to construct the numerical model for the carbon cycle and water cycle in the small scale watershed, which are calibrated and verified by field observations. The developed coupling model for the small scale watershed is extended to a large scale watershed considering the scale effect of model parameters and proper model structure simplification. The large scale watershed model is used to study water cycle and carbon cycle in Lijiang rivershed, and to calculate the carbon flux and carbon sinks in the Lijiang river basin. The study results provide scientific methods for water resources management and environmental protection in southwest karst region corresponding to global climate change. This study could provide basic theory and simulation method for geological carbon sequestration in China karst region.</p> </li> <li> <p><a target="_blank" rel="noopener noreferrer" onclick="trackOutboundLink('http://adsabs.harvard.edu/abs/2003PhDT.......212M','NASAADS'); return false;" href="http://adsabs.harvard.edu/abs/2003PhDT.......212M"><span>Passive load follow analysis of the STAR-LM and STAR-H2 systems</span></a></p> <p><a target="_blank" rel="noopener noreferrer" href="http://adsabs.harvard.edu/abstract_service.html">NASA Astrophysics Data System (ADS)</a></p> <p>Moisseytsev, Anton</p> <p></p> <p>A steady-state model for the calculation of temperature and pressure distributions, and heat and work balance for the STAR-LM and the STAR-H2 systems was developed. The STAR-LM system is designed for electricity production and consists of the lead cooled reactor on natural circulation and the supercritical carbon dioxide Brayton cycle. The STAR-H2 system uses the same reactor which is coupled to the hydrogen production plant, the Brayton cycle, and the water desalination plant. The Brayton cycle produces electricity for the on-site needs. Realistic modules for each system component were developed. The model also performs design calculations for the turbine and compressors for the CO2 Brayton cycle. The model was used to optimize the performance of the entire system as well as every system component. The size of each component was calculated. For the 400 MWt reactor power the STAR-LM produces 174.4 MWe (44% efficiency) and the STAR-H2 system produces 7450 kg H2/hr. The steady state model was used to conduct quasi-static passive load follow analysis. The control strategy was developed for each system; no control action on the reactor is required. As a main safety criterion, the peak cladding temperature is used. It was demonstrated that this temperature remains below the safety limit during both normal operation and load follow.</p> </li> <li> <p><a target="_blank" rel="noopener noreferrer" onclick="trackOutboundLink('http://www.dtic.mil/docs/citations/ADA322259','DTIC-ST'); return false;" href="http://www.dtic.mil/docs/citations/ADA322259"><span>The 1994 Arctic Ocean Section. The First Major Scientific Crossing of the Arctic Ocean,</span></a></p> <p><a target="_blank" rel="noopener noreferrer" href="http://www.dtic.mil/">DTIC Science & Technology</a></p> <p></p> <p>1996-09-01</p> <p>contribute to the international effort to better understand the role of the Arctic Ocean in the global carbon cycle and climate change. Summar...Barium Distributions in the Arctic Ocean ? ........................ 32 Biology and the Carbon Cycle Cycling of Organic Carbon in the Central Arctic...of Heterotrophic Bacteria and Protists in the Arctic Ocean Carbon Cycle............. 40</p> </li> <li> <p><a target="_blank" rel="noopener noreferrer" onclick="trackOutboundLink('https://www.ncbi.nlm.nih.gov/pubmed/24558378','PUBMED'); return false;" href="https://www.ncbi.nlm.nih.gov/pubmed/24558378"><span>Variability of carbon and water fluxes following climate extremes over a tropical forest in southwestern Amazonia.</span></a></p> <p><a target="_blank" rel="noopener noreferrer" href="https://www.ncbi.nlm.nih.gov/entrez/query.fcgi?DB=pubmed">PubMed</a></p> <p>Zeri, Marcelo; Sá, Leonardo D A; Manzi, Antônio O; Araújo, Alessandro C; Aguiar, Renata G; von Randow, Celso; Sampaio, Gilvan; Cardoso, Fernando L; Nobre, Carlos A</p> <p>2014-01-01</p> <p>The carbon and water cycles for a southwestern Amazonian forest site were investigated using the longest time series of fluxes of CO2 and water vapor ever reported for this site. The period from 2004 to 2010 included two severe droughts (2005 and 2010) and a flooding year (2009). The effects of such climate extremes were detected in annual sums of fluxes as well as in other components of the carbon and water cycles, such as gross primary production and water use efficiency. Gap-filling and flux-partitioning were applied in order to fill gaps due to missing data, and errors analysis made it possible to infer the uncertainty on the carbon balance. Overall, the site was found to have a net carbon uptake of ≈5 t C ha(-1) year(-1), but the effects of the drought of 2005 were still noticed in 2006, when the climate disturbance caused the site to become a net source of carbon to the atmosphere. Different regions of the Amazon forest might respond differently to climate extremes due to differences in dry season length, annual precipitation, species compositions, albedo and soil type. Longer time series of fluxes measured over several locations are required to better characterize the effects of climate anomalies on the carbon and water balances for the whole Amazon region. Such valuable datasets can also be used to calibrate biogeochemical models and infer on future scenarios of the Amazon forest carbon balance under the influence of climate change.</p> </li> <li> <p><a target="_blank" rel="noopener noreferrer" onclick="trackOutboundLink('https://www.pubmedcentral.nih.gov/articlerender.fcgi?tool=pmcentrez&artid=3928111','PMC'); return false;" href="https://www.pubmedcentral.nih.gov/articlerender.fcgi?tool=pmcentrez&artid=3928111"><span>Variability of Carbon and Water Fluxes Following Climate Extremes over a Tropical Forest in Southwestern Amazonia</span></a></p> <p><a target="_blank" rel="noopener noreferrer" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?DB=pmc">PubMed Central</a></p> <p>Zeri, Marcelo; Sá, Leonardo D. A.; Manzi, Antônio O.; Araújo, Alessandro C.; Aguiar, Renata G.; von Randow, Celso; Sampaio, Gilvan; Cardoso, Fernando L.; Nobre, Carlos A.</p> <p>2014-01-01</p> <p>The carbon and water cycles for a southwestern Amazonian forest site were investigated using the longest time series of fluxes of CO2 and water vapor ever reported for this site. The period from 2004 to 2010 included two severe droughts (2005 and 2010) and a flooding year (2009). The effects of such climate extremes were detected in annual sums of fluxes as well as in other components of the carbon and water cycles, such as gross primary production and water use efficiency. Gap-filling and flux-partitioning were applied in order to fill gaps due to missing data, and errors analysis made it possible to infer the uncertainty on the carbon balance. Overall, the site was found to have a net carbon uptake of ≈5 t C ha−1 year−1, but the effects of the drought of 2005 were still noticed in 2006, when the climate disturbance caused the site to become a net source of carbon to the atmosphere. Different regions of the Amazon forest might respond differently to climate extremes due to differences in dry season length, annual precipitation, species compositions, albedo and soil type. Longer time series of fluxes measured over several locations are required to better characterize the effects of climate anomalies on the carbon and water balances for the whole Amazon region. Such valuable datasets can also be used to calibrate biogeochemical models and infer on future scenarios of the Amazon forest carbon balance under the influence of climate change. PMID:24558378</p> </li> <li> <p><a target="_blank" rel="noopener noreferrer" onclick="trackOutboundLink('http://adsabs.harvard.edu/abs/2013AGUFM.B33C0495S','NASAADS'); return false;" href="http://adsabs.harvard.edu/abs/2013AGUFM.B33C0495S"><span>Microbial Priming and Protected Carbon Responses to Elevated CO2 at Local to Global Scales: a New Modeling Approach</span></a></p> <p><a target="_blank" rel="noopener noreferrer" href="http://adsabs.harvard.edu/abstract_service.html">NASA Astrophysics Data System (ADS)</a></p> <p>Sulman, B. N.; Oishi, C.; Shevliakova, E.; Pacala, S. W.</p> <p>2013-12-01</p> <p>The soil carbon formulations commonly used in global carbon cycle models and Earth System models (ESMs) are based on first-order decomposition equations, where turnover of carbon is determined only by the size of the carbon pool and empirical functions of responses to temperature and moisture. These models do not include microbial dynamics or protection of carbon in microaggregates and mineral complexes, making them incapable of simulating important soil processes like priming and the influence of soil physical structure on carbon turnover. We present a new soil carbon dynamics model - Carbon, Organisms, Respiration, and Protection in the Soil Environment (CORPSE) - that explicitly represents microbial biomass and protected carbon pools. The model includes multiple types of carbon with different chemically determined turnover rates that interact with a single dynamic microbial biomass pool, allowing the model to simulate priming effects. The model also includes the formation and turnover of protected carbon that is inaccessible to microbial decomposers. The rate of protected carbon formation increases with microbial biomass. CORPSE has been implemented both as a stand-alone model and as a component of the NOAA Geophysical Fluid Dynamics Laboratory (GFDL) ESM. We calibrated the model against measured soil carbon stocks from the Duke FACE experiment. The model successfully simulated the seasonal pattern of heterotrophic CO2 production. We investigated the roles of priming and protection in soil carbon accumulation by running the model using measured inputs of leaf litter, fine roots, and root exudates from the ambient and elevated CO2 plots at the Duke FACE experiment. Measurements from the experiment showed that elevated CO2 caused enhanced root exudation, increasing soil carbon turnover in the rhizosphere due to priming effects. We tested the impact of increased root exudation on soil carbon accumulation by comparing model simulations of carbon accumulation under elevated CO2 with and without increased root exudation. Increased root exudation stimulated microbial activity in the model, resulting in reduced accumulation of chemically recalcitrant carbon, but increasing the formation of protected carbon. This indicates that elevated CO2 could cause decreases in soil carbon storage despite increases in productivity in ecosystems where protection of soil carbon is limited. These effects have important implications for simulations of soil carbon response to elevated CO2 in current terrestrial carbon cycle models. The CORPSE model has been implemented in LM3, the terrestrial component of the GFDL ESM. In addition to the functionality described above, this model adds vertically resolved carbon pools and vertical transfers of carbon, leading to a decrease in carbon turnover rates with depth due to leaching of priming agents from the surface. We present preliminary global simulations using this model, including the variation of microbial activity and protected carbon with latitude and the resulting impacts on the sensitivity of soil carbon to climatic warming.</p> </li> </ol> <div class="pull-right"> <ul class="pagination"> <li><a href="#" onclick='return showDiv("page_1");'>«</a></li> <li><a href="#" onclick='return showDiv("page_13");'>13</a></li> <li><a href="#" onclick='return showDiv("page_14");'>14</a></li> <li class="active"><span>15</span></li> <li><a href="#" onclick='return showDiv("page_16");'>16</a></li> <li><a href="#" onclick='return showDiv("page_17");'>17</a></li> <li><a href="#" onclick='return showDiv("page_25");'>»</a></li> </ul> </div> </div><!-- col-sm-12 --> </div><!-- row --> </div><!-- page_15 --> <div id="page_16" class="hiddenDiv"> <div class="row"> <div class="col-sm-12"> <div class="pull-right"> <ul class="pagination"> <li><a href="#" onclick='return showDiv("page_1");'>«</a></li> <li><a href="#" onclick='return showDiv("page_14");'>14</a></li> <li><a href="#" onclick='return showDiv("page_15");'>15</a></li> <li class="active"><span>16</span></li> <li><a href="#" onclick='return showDiv("page_17");'>17</a></li> <li><a href="#" onclick='return showDiv("page_18");'>18</a></li> <li><a href="#" onclick='return showDiv("page_25");'>»</a></li> </ul> </div> </div> </div> <div class="row"> <div class="col-sm-12"> <ol class="result-class" start="301"> <li> <p><a target="_blank" rel="noopener noreferrer" onclick="trackOutboundLink('https://www.ncbi.nlm.nih.gov/pubmed/28477814','PUBMED'); return false;" href="https://www.ncbi.nlm.nih.gov/pubmed/28477814"><span>Carbon flow analysis of China's agro-ecosystem from 1980 to 2013: A perspective from substance flow analysis.</span></a></p> <p><a target="_blank" rel="noopener noreferrer" href="https://www.ncbi.nlm.nih.gov/entrez/query.fcgi?DB=pubmed">PubMed</a></p> <p>Liu, Yu; Wang, Can; Chen, Minpeng</p> <p>2017-05-01</p> <p>Research on carbon cycling has attracted attention from both scientists and policy-makers. Based on material flow analysis, this study systematically budgets the carbon inputs, outputs and balance from 1980 to 2013 for China's agro-ecosystem and its sub-systems, including agricultural land use, livestock breeding and rural life. The results show that from 1980 to 2013, both the carbon input and output were growing gradually, with the carbon input doubling from 1.6PgC/year in 1980 to 3.4PgC/year in 2013, while carbon output grew from 2.2PgC/year in 1980 to 3.8PgC/year in 2013. From 1980 to 2013, the crop production system in China has remained a carbon source, and the agricultural land uses were also almost all carbon sources instead of carbon sinks. As soil carbon stock plays a very important role in deciding the function of China's agro-ecosystem as a carbon sink or source, practices that can promote carbon storage and sequestration will be an essential component of low carbon agriculture development in China. Copyright © 2016. Published by Elsevier B.V.</p> </li> <li> <p><a target="_blank" rel="noopener noreferrer" onclick="trackOutboundLink('https://www.osti.gov/pages/biblio/1265927-remote-sensing-based-estimation-annual-soil-respiration-two-contrasting-forest-sites','SCIGOV-DOEP'); return false;" href="https://www.osti.gov/pages/biblio/1265927-remote-sensing-based-estimation-annual-soil-respiration-two-contrasting-forest-sites"><span>Remote sensing-based estimation of annual soil respiration at two contrasting forest sites</span></a></p> <p><a target="_blank" rel="noopener noreferrer" href="http://www.osti.gov/pages">DOE PAGES</a></p> <p>Gu, Lianhong; Huang, Ni; Black, T. Andrew; ...</p> <p>2015-11-23</p> <p>Soil respiration (R s), an important component of the global carbon cycle, can be estimated using remotely sensed data, but the accuracy of this technique has not been thoroughly investigated. In this article, we proposed a methodology for the remote estimation of annual R s at two contrasting FLUXNET forest sites (a deciduous broadleaf forest and an evergreen needleleaf forest).</p> </li> <li> <p><a target="_blank" rel="noopener noreferrer" onclick="trackOutboundLink('https://www.fs.usda.gov/treesearch/pubs/30199','TREESEARCH'); return false;" href="https://www.fs.usda.gov/treesearch/pubs/30199"><span>Coarse woody debris in undisturbed and logged forests in the eastern Brazilian Amazon.</span></a></p> <p><a target="_blank" rel="noopener noreferrer" href="http://www.fs.usda.gov/treesearch/">Treesearch</a></p> <p>Michael Keller; Michael Palace; Gregory P. Asner; Rodrigo Jr. Pereira; Jose Natalino M. Silva</p> <p>2004-01-01</p> <p>Coarse woody debris (CWD) is an important component of the carbon cycle in tropical forests. We measured the volume and density of fallen CWD at two sites, Cauaxi and Tapajós in the Eastern Amazon. At both sites we studied undisturbed forests (UFs) and logged forests 1 year after harvest. Conventional logging (CL) and reduced impact logging (RIL) were...</p> </li> <li> <p><a target="_blank" rel="noopener noreferrer" onclick="trackOutboundLink('http://adsabs.harvard.edu/abs/2017GeoRL..4412484C','NASAADS'); return false;" href="http://adsabs.harvard.edu/abs/2017GeoRL..4412484C"><span>Simulated Effect of Carbon Cycle Feedback on Climate Response to Solar Geoengineering</span></a></p> <p><a target="_blank" rel="noopener noreferrer" href="http://adsabs.harvard.edu/abstract_service.html">NASA Astrophysics Data System (ADS)</a></p> <p>Cao, Long; Jiang, Jiu</p> <p>2017-12-01</p> <p>Most modeling studies investigate climate effects of solar geoengineering under prescribed atmospheric CO2, thereby neglecting potential climate feedbacks from the carbon cycle. Here we use an Earth system model to investigate interactive feedbacks between solar geoengineering, global carbon cycle, and climate change. We design idealized sunshade geoengineering simulations to prevent global warming from exceeding 2°C above preindustrial under a CO2 emission scenario with emission mitigation starting from middle of century. By year 2100, solar geoengineering reduces the burden of atmospheric CO2 by 47 PgC with enhanced carbon storage in the terrestrial biosphere. As a result of reduced atmospheric CO2, consideration of the carbon cycle feedback reduces required insolation reduction in 2100 from 2.0 to 1.7 W m-2. With higher climate sensitivity the effect from carbon cycle feedback becomes more important. Our study demonstrates the importance of carbon cycle feedback in climate response to solar geoengineering.</p> </li> <li> <p><a target="_blank" rel="noopener noreferrer" onclick="trackOutboundLink('http://www.osti.gov/sciencecinema/biblio/1015167','SCIGOVIMAGE-SCICINEMA'); return false;" href="http://www.osti.gov/sciencecinema/biblio/1015167"><span>Carbon Capture (Carbon Cycle 2.0)</span></a></p> <p><a target="_blank" rel="noopener noreferrer" href="http://www.osti.gov/sciencecinema/">ScienceCinema</a></p> <p>Smit, Berend</p> <p>2018-04-26</p> <p>Berend Smit speaks at the Carbon Cycle 2.0 kick-off symposium Feb. 3, 2010. We emit more carbon into the atmosphere than natural processes are able to remove - an imbalance with negative consequences. Carbon Cycle 2.0 is a Berkeley Lab initiative to provide the science needed to restore this balance by integrating the labs diverse research activities and delivering creative solutions toward a carbon-neutral energy future.</p> </li> <li> <p><a target="_blank" rel="noopener noreferrer" onclick="trackOutboundLink('http://adsabs.harvard.edu/abs/2017AGUFM.H53L..02H','NASAADS'); return false;" href="http://adsabs.harvard.edu/abs/2017AGUFM.H53L..02H"><span>Field Investigation and Modeling Development for Hydrological and Carbon Cycles in Southwest Karst Region of China</span></a></p> <p><a target="_blank" rel="noopener noreferrer" href="http://adsabs.harvard.edu/abstract_service.html">NASA Astrophysics Data System (ADS)</a></p> <p>Hu, X. B.</p> <p>2017-12-01</p> <p>It is required to understanding water cycle and carbon cycle processes for water resource management and pollution prevention and global warming influence in southwest karst region of China. Lijiang river basin is selected as our study region. Interdisciplinary field and laboratory experiments with various technologies are conducted to characterize the karst aquifers in detail. Key processes in the karst water cycle and carbon cycle are determined. Based on the MODFLOW-CFP model, new watershed flow and carbon cycle models are developed coupled subsurface and surface water flow models. Our study focus on the karst springshed in Mao village, the mechanisms coupling carbon cycle and water cycle are explored. This study provides basic theory and simulation method for water resource management and groundwater pollution prevention in China karst region.</p> </li> <li> <p><a target="_blank" rel="noopener noreferrer" onclick="trackOutboundLink('https://pubs.er.usgs.gov/publication/70182176','USGSPUBS'); return false;" href="https://pubs.er.usgs.gov/publication/70182176"><span>Ebullitive methane emissions from oxygenated wetland streams</span></a></p> <p><a target="_blank" rel="noopener noreferrer" href="http://pubs.er.usgs.gov/pubs/index.jsp?view=adv">USGS Publications Warehouse</a></p> <p>Crawford, John T.; Stanley, Emily H.; Spawn, Seth A.; Finlay, Jacques C.; Striegl, Robert G.</p> <p>2014-01-01</p> <p>Stream and river carbon dioxide emissions are an important component of the global carbon cycle. Methane emissions from streams could also contribute to regional or global greenhouse gas cycling, but there are relatively few data regarding stream and river methane emissions. Furthermore, the available data do not typically include the ebullitive (bubble-mediated) pathway, instead focusing on emission of dissolved methane by diffusion or convection. Here, we show the importance of ebullitive methane emissions from small streams in the regional greenhouse gas balance of a lake and wetland-dominated landscape in temperate North America and identify the origin of the methane emitted from these well-oxygenated streams. Stream methane flux densities from this landscape tended to exceed those of nearby wetland diffusive fluxes as well as average global wetland ebullitive fluxes. Total stream ebullitive methane flux at the regional scale (103 Mg C yr−1; over 6400 km2) was of the same magnitude as diffusive methane flux previously documented at the same scale. Organic-rich stream sediments had the highest rates of bubble release and higher enrichment of methane in bubbles, but glacial sand sediments also exhibited high bubble emissions relative to other studied environments. Our results from a database of groundwater chemistry support the hypothesis that methane in bubbles is produced in anoxic near-stream sediment porewaters, and not in deeper, oxygenated groundwaters. Methane interacts with other key elemental cycles such as nitrogen, oxygen, and sulfur, which has implications for ecosystem changes such as drought and increased nutrient loading. Our results support the contention that streams, particularly those draining wetland landscapes of the northern hemisphere, are an important component of the global methane cycle.</p> </li> <li> <p><a target="_blank" rel="noopener noreferrer" onclick="trackOutboundLink('http://adsabs.harvard.edu/abs/2017AGUFMDI51B0310C','NASAADS'); return false;" href="http://adsabs.harvard.edu/abs/2017AGUFMDI51B0310C"><span>Effects of sea-level changes on mid-ocean ridge magmatism and implications for emission rates of carbon.</span></a></p> <p><a target="_blank" rel="noopener noreferrer" href="http://adsabs.harvard.edu/abstract_service.html">NASA Astrophysics Data System (ADS)</a></p> <p>Cerpa, N.; Katz, R. F.; Keller, T.</p> <p>2017-12-01</p> <p>Glacial cycles move water between ice sheets and the ocean, and hence cause regional pressure changes in the solid Earth. The rate of sea-level (SL) change during this cycle is comparable to the rate of mantle upwelling beneath mid-ocean ridges (MORs), and hence we expect the induced pressure variations to modify the rate and depth of silicate melting. SL variations may therefore induce changes in the supply and composition of magma at MORs, which could affect the flux of carbon into the climate system. Likewise, the trace-element geochemistry of magmas tapped by ridge volcanism may vary during these cycles due to variations in melt flux. Such variations may have been recorded by sediment-hosted volcanic glass fragments [Ferguson et al., 2017]. We investigate these questions using computational models of melt production and transport in which volatiles participate in the thermodynamics of melting. Published models of the effect of SL on MORs predict up to 10% variation in carbon emission rates for absolute changes in SL of 50-100 m with possible lag times of several tens of kyrs [Burley et al., 2015; Hasenclever et al., 2017]. A major assumption of those models is that water and carbon are passive, incompatible elements. But small concentrations of those volatiles affect the solidus of mantle peridotite and increase the volume of upper mantle undergoing partial melting. Hence the current predictions of variation in MOR carbon emission might be an underestimate. Moreover, published models neglect the effects of volatiles on melt transport. Recents studies have demonstrated that volatiles can induce channelized transport [Keller and Katz 2016], potentially affecting the rate at which carbon is extracted from the mantle. In this study, we investigate the interplay between SL variations, melting, and segregation of volatile-rich melts. We use two-phase magma/mantle dynamics coupled to melting models that treat water and carbon dioxide as thermodynamic components. We compare models of equilibrium and disequilibrium melting to assess the influence of reaction kinetics on magma productivity at MORs during SL variations. Our calculations provide new estimates of the lag and amplitude of carbon emissions during glacial cycles. We address the impact of SL variations on the trace-element composition of magmas.</p> </li> <li> <p><a target="_blank" rel="noopener noreferrer" onclick="trackOutboundLink('https://www.ncbi.nlm.nih.gov/pubmed/25960765','PUBMED'); return false;" href="https://www.ncbi.nlm.nih.gov/pubmed/25960765"><span>Comparison between remote sensing and a dynamic vegetation model for estimating terrestrial primary production of Africa.</span></a></p> <p><a target="_blank" rel="noopener noreferrer" href="https://www.ncbi.nlm.nih.gov/entrez/query.fcgi?DB=pubmed">PubMed</a></p> <p>Ardö, Jonas</p> <p>2015-12-01</p> <p>Africa is an important part of the global carbon cycle. It is also a continent facing potential problems due to increasing resource demand in combination with climate change-induced changes in resource supply. Quantifying the pools and fluxes constituting the terrestrial African carbon cycle is a challenge, because of uncertainties in meteorological driver data, lack of validation data, and potentially uncertain representation of important processes in major ecosystems. In this paper, terrestrial primary production estimates derived from remote sensing and a dynamic vegetation model are compared and quantified for major African land cover types. Continental gross primary production estimates derived from remote sensing were higher than corresponding estimates derived from a dynamic vegetation model. However, estimates of continental net primary production from remote sensing were lower than corresponding estimates from the dynamic vegetation model. Variation was found among land cover classes, and the largest differences in gross primary production were found in the evergreen broadleaf forest. Average carbon use efficiency (NPP/GPP) was 0.58 for the vegetation model and 0.46 for the remote sensing method. Validation versus in situ data of aboveground net primary production revealed significant positive relationships for both methods. A combination of the remote sensing method with the dynamic vegetation model did not strongly affect this relationship. Observed significant differences in estimated vegetation productivity may have several causes, including model design and temperature sensitivity. Differences in carbon use efficiency reflect underlying model assumptions. Integrating the realistic process representation of dynamic vegetation models with the high resolution observational strength of remote sensing may support realistic estimation of components of the carbon cycle and enhance resource monitoring, providing suitable validation data is available.</p> </li> <li> <p><a target="_blank" rel="noopener noreferrer" onclick="trackOutboundLink('https://www.ncbi.nlm.nih.gov/pubmed/29540639','PUBMED'); return false;" href="https://www.ncbi.nlm.nih.gov/pubmed/29540639"><span>Different Metabolomic Responses to Carbon Starvation between Light and Dark Conditions in the Purple Photosynthetic Bacterium, Rhodopseudomonas palustris.</span></a></p> <p><a target="_blank" rel="noopener noreferrer" href="https://www.ncbi.nlm.nih.gov/entrez/query.fcgi?DB=pubmed">PubMed</a></p> <p>Kanno, Nanako; Matsuura, Katsumi; Haruta, Shin</p> <p>2018-03-29</p> <p>Purple photosynthetic bacteria utilize light energy for growth. We previously demonstrated that light energy contributed to prolonging the survival of multiple purple bacteria under carbon-starved conditions. In order to clarify the effects of illumination on metabolic states under carbon-starved, non-growing conditions, we herein compared the metabolic profiles of starved cells in the light and dark using the purple bacterium, Rhodopseudomonas palustris. The metabolic profiles of starved cells in the light were markedly different from those in the dark. After starvation for 5 d in the light, cells showed increases in the amount of ATP and the NAD + /NADH ratio. Decreases in the amounts of most metabolites related to glycolysis and the TCA cycle in energy-rich starved cells suggest the active utilization of these metabolites for the modification of cellular components. Starvation in the dark induced the consumption of cellular compounds such as amino acids, indicating that the degradation of these cellular components produced ATP in order to maintain viability under energy-poor conditions. The present results suggest that intracellular energy levels alter survival strategies under carbon-starved conditions through metabolism.</p> </li> <li> <p><a target="_blank" rel="noopener noreferrer" onclick="trackOutboundLink('http://adsabs.harvard.edu/abs/2016EGUGA..1811839S','NASAADS'); return false;" href="http://adsabs.harvard.edu/abs/2016EGUGA..1811839S"><span>Plant competition and the implications for tropical forest carbon dynamics</span></a></p> <p><a target="_blank" rel="noopener noreferrer" href="http://adsabs.harvard.edu/abstract_service.html">NASA Astrophysics Data System (ADS)</a></p> <p>Schnitzer, Stefan</p> <p>2016-04-01</p> <p>Tropical forests store more than one third of all terrestrial carbon and account for over one third of terrestrial net primary productivity, and thus they are a critical component of the global carbon cycle. Nearly all of the aboveground carbon in tropical forests is held in tree biomass, and long-term carbon fluxes are balanced largely by tree growth and tree death. Therefore, the vast majority of research on tropical forest carbon dynamics has focused on the growth and mortality of canopy trees. By contrast, lianas (woody vines) contribute little biomass relative to trees. However, competition between lianas (woody vines) and trees may result in forest-wide carbon loss if lianas fail to accumulate the carbon that they displace in trees. We tested this hypotheses using a series of large-scale liana-removal studies in the Republic of Panama. We found that lianas limited tree growth and increased tree mortality, thus significantly reducing carbon accumulation in trees. Lianas themselves, however, did not compensate for the carbon that they displaced in trees. Lianas lower the capacity of tropical forests to uptake and store carbon, and the recently observed increases in liana abundance in neotropical forests will likely result in further reductions of carbon uptake.</p> </li> <li> <p><a target="_blank" rel="noopener noreferrer" onclick="trackOutboundLink('http://adsabs.harvard.edu/abs/2013GeCoA.117..129Z','NASAADS'); return false;" href="http://adsabs.harvard.edu/abs/2013GeCoA.117..129Z"><span>Mechanistic controls on diverse fates of terrestrial organic components in the East China Sea</span></a></p> <p><a target="_blank" rel="noopener noreferrer" href="http://adsabs.harvard.edu/abstract_service.html">NASA Astrophysics Data System (ADS)</a></p> <p>Zhu, Chun; Wagner, Thomas; Talbot, Helen M.; Weijers, Johan W. H.; Pan, Jian-Ming; Pancost, Richard D.</p> <p>2013-09-01</p> <p>Terrestrial carbon transferred from the land to sea is a critical component of the global carbon cycle. A range of geochemical proxies has been developed to fingerprint the fate of terrestrial organic matter (TOM) in marine sediments. However, discrepancies among different proxies limit our ability to quantify and interpret the terrestrial signals in marine sediments, with consequences for the investigation of both the modern carbon cycle and past environmental change. To mechanistically understand these discrepancies, we examined the distributions of a range of terrestrial proxies and their aquatic counterparts (i.e. marine proxies) in the Yangtze river-East China Sea (YR-ECS) shelf system, where TOM experiences extensive modification during transport and burial. TOM proxies in the YR-ECS system collectively fit a power-law model but with distinct attenuation rates (the a∗ values) for individual molecular proxy groups. Among a range of TOM proxies, the modeled a∗ values decrease in the order: soil-marker BHPs > triterpenols > lignin > HMW n-alkanols > branched GDGTs > HMW n-alkanes for biomarkers; and Rsoil > BIT > %TOMiso for proxies tracing %TOM. Rapid loss of TOM components through dissociation in the narrow estuary, followed by oxidation over the wide open shelf, are best described by power curves. Inherent chemical reactivity (i.e. the number of functional groups), responses to hydraulic sorting, and in situ production regulate the individual attenuation rates. Of them, chemical reactivity plays the most important role on proxy behavior, supported by a strong correlation between a∗ values and standard molal Gibbs energies. Both, physical protection and chemical reactivity fundamentally control the overall behavior of TOM components, with the relative importance being setting-dependant: The former is relatively important in the estuary, whereas the later is the primary control over the open shelf. Moreover, regional variation of different marine-counterparts is also significant over the river-ECS shelf system, seemingly regulated by regional nutrient distributions. Therefore, for %TOM estimates using molecular ratio approaches, the specific behavior of individual terrestrial components and marine-counterparts and the physical, biological and chemical characteristics of depositional settings all need to be considered.</p> </li> <li> <p><a target="_blank" rel="noopener noreferrer" onclick="trackOutboundLink('http://adsabs.harvard.edu/abs/2015GeoRL..42.8624L','NASAADS'); return false;" href="http://adsabs.harvard.edu/abs/2015GeoRL..42.8624L"><span>Temperature acclimation of photosynthesis and respiration: A key uncertainty in the carbon cycle-climate feedback</span></a></p> <p><a target="_blank" rel="noopener noreferrer" href="http://adsabs.harvard.edu/abstract_service.html">NASA Astrophysics Data System (ADS)</a></p> <p>Lombardozzi, Danica L.; Bonan, Gordon B.; Smith, Nicholas G.; Dukes, Jeffrey S.; Fisher, Rosie A.</p> <p>2015-10-01</p> <p>Earth System Models typically use static responses to temperature to calculate photosynthesis and respiration, but experimental evidence suggests that many plants acclimate to prevailing temperatures. We incorporated representations of photosynthetic and leaf respiratory temperature acclimation into the Community Land Model, the terrestrial component of the Community Earth System Model. These processes increased terrestrial carbon pools by 20 Pg C (22%) at the end of the 21st century under a business-as-usual (Representative Concentration Pathway 8.5) climate scenario. Including the less certain estimates of stem and root respiration acclimation increased terrestrial carbon pools by an additional 17 Pg C (~40% overall increase). High latitudes gained the most carbon with acclimation, and tropical carbon pools increased least. However, results from both of these regions remain uncertain; few relevant data exist for tropical and boreal plants or for extreme temperatures. Constraining these uncertainties will produce more realistic estimates of land carbon feedbacks throughout the 21st century.</p> </li> <li> <p><a target="_blank" rel="noopener noreferrer" onclick="trackOutboundLink('https://eric.ed.gov/?q=cycling&id=EJ1170002','ERIC'); return false;" href="https://eric.ed.gov/?q=cycling&id=EJ1170002"><span>Assessing Students' Disciplinary and Interdisciplinary Understanding of Global Carbon Cycling</span></a></p> <p><a target="_blank" rel="noopener noreferrer" href="http://www.eric.ed.gov/ERICWebPortal/search/extended.jsp?_pageLabel=advanced">ERIC Educational Resources Information Center</a></p> <p>You, Hye Sun; Marshall, Jill A.; Delgado, Cesar</p> <p>2018-01-01</p> <p>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…</p> </li> <li> <p><a target="_blank" rel="noopener noreferrer" onclick="trackOutboundLink('https://www.pubmedcentral.nih.gov/articlerender.fcgi?tool=pmcentrez&artid=4213077','PMC'); return false;" href="https://www.pubmedcentral.nih.gov/articlerender.fcgi?tool=pmcentrez&artid=4213077"><span>Dynamics of Carbon-Concentrating Mechanism Induction and Protein Relocalization during the Dark-to-Light Transition in Synchronized Chlamydomonas reinhardtii1[W][OPEN</span></a></p> <p><a target="_blank" rel="noopener noreferrer" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?DB=pmc">PubMed Central</a></p> <p>Mitchell, Madeline C.; Meyer, Moritz T.; Griffiths, Howard</p> <p>2014-01-01</p> <p>In the model green alga Chlamydomonas reinhardtii, a carbon-concentrating mechanism (CCM) is induced under low CO2 in the light and comprises active inorganic carbon transport components, carbonic anhydrases, and aggregation of Rubisco in the chloroplast pyrenoid. Previous studies have focused predominantly on asynchronous cultures of cells grown under low versus high CO2. Here, we have investigated the dynamics of CCM activation in synchronized cells grown in dark/light cycles compared with induction under low CO2. The specific focus was to undertake detailed time course experiments comparing physiology and gene expression during the dark-to-light transition. First, the CCM could be fully induced 1 h before dawn, as measured by the photosynthetic affinity for inorganic carbon. This occurred in advance of maximum gene transcription and protein accumulation and contrasted with the coordinated induction observed under low CO2. Between 2 and 1 h before dawn, the proportion of Rubisco and the thylakoid lumen carbonic anhydrase in the pyrenoid rose substantially, coincident with increased CCM activity. Thus, other mechanisms are likely to activate the CCM before dawn, independent of gene transcription of known CCM components. Furthermore, this study highlights the value of using synchronized cells during the dark-to-light transition as an alternative means of investigating CCM induction. PMID:25106822</p> </li> <li> <p><a target="_blank" rel="noopener noreferrer" onclick="trackOutboundLink('https://www.pubmedcentral.nih.gov/articlerender.fcgi?tool=pmcentrez&artid=4063024','PMC'); return false;" href="https://www.pubmedcentral.nih.gov/articlerender.fcgi?tool=pmcentrez&artid=4063024"><span>A Real-Time Recording Model of Key Indicators for Energy Consumption and Carbon Emissions of Sustainable Buildings</span></a></p> <p><a target="_blank" rel="noopener noreferrer" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?DB=pmc">PubMed Central</a></p> <p>Wu, Weiwei; Yang, Huanjia; Chew, David; Hou, Yanhong; Li, Qiming</p> <p>2014-01-01</p> <p>Buildings' sustainability is one of the crucial parts for achieving urban sustainability. Applied to buildings, life-cycle assessment encompasses the analysis and assessment of the environmental effects of building materials, components and assemblies throughout the entire life of the building construction, use and demolition. Estimate of carbon emissions is essential and crucial for an accurate and reasonable life-cycle assessment. Addressing the need for more research into integrating analysis of real-time and automatic recording of key indicators for a more accurate calculation and comparison, this paper aims to design a real-time recording model of these crucial indicators concerning the calculation and estimation of energy use and carbon emissions of buildings based on a Radio Frequency Identification (RFID)-based system. The architecture of the RFID-based carbon emission recording/tracking system, which contains four functional layers including data record layer, data collection/update layer, data aggregation layer and data sharing/backup layer, is presented. Each of these layers is formed by RFID or network devices and sub-systems that operate at a specific level. In the end, a proof-of-concept system is developed to illustrate the implementation of the proposed architecture and demonstrate the feasibility of the design. This study would provide the technical solution for real-time recording system of building carbon emissions and thus is of great significance and importance to improve urban sustainability. PMID:24831109</p> </li> <li> <p><a target="_blank" rel="noopener noreferrer" onclick="trackOutboundLink('https://www.pubmedcentral.nih.gov/articlerender.fcgi?tool=pmcentrez&artid=3618115','PMC'); return false;" href="https://www.pubmedcentral.nih.gov/articlerender.fcgi?tool=pmcentrez&artid=3618115"><span>High Spatial Resolution Infrared Micro-Spectroscopy Reveals the Mechanism of Leaf Lignin Decomposition by Aquatic Fungi</span></a></p> <p><a target="_blank" rel="noopener noreferrer" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?DB=pmc">PubMed Central</a></p> <p>Kerr, Janice L.; Baldwin, Darren S.; Tobin, Mark J.; Puskar, Ljiljana; Kappen, Peter; Rees, Gavin N.; Silvester, Ewen</p> <p>2013-01-01</p> <p>Organic carbon is a critical component of aquatic systems, providing energy storage and transfer between organisms. Fungi are a major decomposer group in the aquatic carbon cycle, and are one of few groups thought to be capable of breaking down woody (lignified) tissue. In this work we have used high spatial resolution (synchrotron light source) infrared micro-spectroscopy to study the interaction between aquatic fungi and lignified leaf vein material (xylem) from River Redgum trees (E. camaldulensis) endemic to the lowland rivers of South-Eastern Australia. The work provides spatially explicit evidence that fungal colonisation of leaf litter involves the oxidative breakdown of lignin immediately adjacent to the fungal tissue and depletion of the lignin-bound cellulose. Cellulose depletion occurs over relatively short length scales (5–15 µm) and highlights the likely importance of mechanical breakdown in accessing the carbohydrate content of this resource. Low bioavailability compounds (oxidized lignin and polyphenols of plant origin) remain in colonised leaves, even after fungal activity diminishes, and suggests a possible pathway for the sequestration of carbon in wetlands. The work shows that fungi likely have a critical role in the partitioning of lignified material into a biodegradable fraction that can re-enter the aquatic carbon cycle, and a recalcitrant fraction that enters long-term storage in sediments or contribute to the formation of dissolved organic carbon in the water column. PMID:23577169</p> </li> <li> <p><a target="_blank" rel="noopener noreferrer" onclick="trackOutboundLink('https://www.ncbi.nlm.nih.gov/pubmed/24831109','PUBMED'); return false;" href="https://www.ncbi.nlm.nih.gov/pubmed/24831109"><span>A real-time recording model of key indicators for energy consumption and carbon emissions of sustainable buildings.</span></a></p> <p><a target="_blank" rel="noopener noreferrer" href="https://www.ncbi.nlm.nih.gov/entrez/query.fcgi?DB=pubmed">PubMed</a></p> <p>Wu, Weiwei; Yang, Huanjia; Chew, David; Hou, Yanhong; Li, Qiming</p> <p>2014-05-14</p> <p>Buildings' sustainability is one of the crucial parts for achieving urban sustainability. Applied to buildings, life-cycle assessment encompasses the analysis and assessment of the environmental effects of building materials, components and assemblies throughout the entire life of the building construction, use and demolition. Estimate of carbon emissions is essential and crucial for an accurate and reasonable life-cycle assessment. Addressing the need for more research into integrating analysis of real-time and automatic recording of key indicators for a more accurate calculation and comparison, this paper aims to design a real-time recording model of these crucial indicators concerning the calculation and estimation of energy use and carbon emissions of buildings based on a Radio Frequency Identification (RFID)-based system. The architecture of the RFID-based carbon emission recording/tracking system, which contains four functional layers including data record layer, data collection/update layer, data aggregation layer and data sharing/backup layer, is presented. Each of these layers is formed by RFID or network devices and sub-systems that operate at a specific level. In the end, a proof-of-concept system is developed to illustrate the implementation of the proposed architecture and demonstrate the feasibility of the design. This study would provide the technical solution for real-time recording system of building carbon emissions and thus is of great significance and importance to improve urban sustainability.</p> </li> <li> <p><a target="_blank" rel="noopener noreferrer" onclick="trackOutboundLink('http://adsabs.harvard.edu/abs/2017EGUGA..19..320N','NASAADS'); return false;" href="http://adsabs.harvard.edu/abs/2017EGUGA..19..320N"><span>Representation of Dissolved Organic Carbon in the JULES Dynamic Global Vegetation Model</span></a></p> <p><a target="_blank" rel="noopener noreferrer" href="http://adsabs.harvard.edu/abstract_service.html">NASA Astrophysics Data System (ADS)</a></p> <p>Nakhavali, Mahdi; Friedlingstein, Pierre; Guenet, Bertrand; Ciais, Philip</p> <p>2017-04-01</p> <p>Current global models of the carbon cycle consider only vertical gas exchanges between terrestrial or oceanic reservoirs and the atmosphere, hence not considering lateral transport of carbon from the continent to the oceans. This also means that such models implicitly consider that all the CO2 which is not respired to the atmosphere is stored on land, hence overestimating the land sink of carbon. Moving toward a boundless carbon cycle that is integrating the whole continuum from land to ocean to atmosphere is needed in order to better understand Earth's carbon cycle and to make more reliable projection of its future. Here we present an original representation of Dissolved Organic Carbon (DOC) processes in the Joint UK Land Environment Simulator (JULES). The standard version of JULES represent energy, water and carbon cycles and exchanges with the atmosphere, but only account for water run-off, not including export of carbon from terrestrial ecosystems to the aquatic environments. The aim of the project is to include in JULES a representation of DOC production in terrestrial soils, due to incomplete decomposition of organic matter, its decomposition to the atmosphere, and its export to the river network by leaching. In new developed version of JULES (JULES-DOCM), DOC pools, based on their decomposition rate, are classified into labile and recalcitrant within 3 meters of soil. Based on turnover rate, DOC coming from plant material pools and microbial biomass is directed to labile pool, while DOC from humus is directed to recalcitrant pool. Both of these pools have free (dissolved) and locked (adsorbed) form where just the free pool is subjected to decomposition and leaching. DOC production and decomposition are controlled by rate modifiers (moisture, temperature, vegetation fraction and decomposition rate) at each soil layer. Decomposed DOC is released to the atmosphere following a fixed carbon use efficiency. Leaching accounts for both surface (runoff) and subsurface (groundwater) components and is parameterized as Top soil leaching (from top 20cm) and Bottom soil leaching (down to 3 meters) depending on DOC concentration and runoff leaving that layer. The model parameters are calibrated against specific sites (Brasschaat, Hainich and Carlow) for which observations of DOC concentration and leaching are available. Tuning is performed optimizing parameters such as DOC labile and recalcitrant resident time, DOC vertical distribution and CUE. Once this calibration has been performed at the site level, the model is used for global simulations with the major historical forcing (climate, atmospheric CO2 and land-use changes) in order to estimate the changes of DOC export and their attribution to anthropogenic activities.</p> </li> <li> <p><a target="_blank" rel="noopener noreferrer" onclick="trackOutboundLink('https://www.ncbi.nlm.nih.gov/pubmed/24429523','PUBMED'); return false;" href="https://www.ncbi.nlm.nih.gov/pubmed/24429523"><span>Rate of tree carbon accumulation increases continuously with tree size.</span></a></p> <p><a target="_blank" rel="noopener noreferrer" href="https://www.ncbi.nlm.nih.gov/entrez/query.fcgi?DB=pubmed">PubMed</a></p> <p>Stephenson, N L; Das, A J; Condit, R; Russo, S E; Baker, P J; Beckman, N G; Coomes, D A; Lines, E R; Morris, W K; Rüger, N; Alvarez, E; Blundo, C; Bunyavejchewin, S; Chuyong, G; Davies, S J; Duque, A; Ewango, C N; Flores, O; Franklin, J F; Grau, H R; Hao, Z; Harmon, M E; Hubbell, S P; Kenfack, D; Lin, Y; Makana, J-R; Malizia, A; Malizia, L R; Pabst, R J; Pongpattananurak, N; Su, S-H; Sun, I-F; Tan, S; Thomas, D; van Mantgem, P J; Wang, X; Wiser, S K; Zavala, M A</p> <p>2014-03-06</p> <p>Forests are major components of the global carbon cycle, providing substantial feedback to atmospheric greenhouse gas concentrations. Our ability to understand and predict changes in the forest carbon cycle--particularly net primary productivity and carbon storage--increasingly relies on models that represent biological processes across several scales of biological organization, from tree leaves to forest stands. Yet, despite advances in our understanding of productivity at the scales of leaves and stands, no consensus exists about the nature of productivity at the scale of the individual tree, in part because we lack a broad empirical assessment of whether rates of absolute tree mass growth (and thus carbon accumulation) decrease, remain constant, or increase as trees increase in size and age. Here we present a global analysis of 403 tropical and temperate tree species, showing that for most species mass growth rate increases continuously with tree size. Thus, large, old trees do not act simply as senescent carbon reservoirs but actively fix large amounts of carbon compared to smaller trees; at the extreme, a single big tree can add the same amount of carbon to the forest within a year as is contained in an entire mid-sized tree. The apparent paradoxes of individual tree growth increasing with tree size despite declining leaf-level and stand-level productivity can be explained, respectively, by increases in a tree's total leaf area that outpace declines in productivity per unit of leaf area and, among other factors, age-related reductions in population density. Our results resolve conflicting assumptions about the nature of tree growth, inform efforts to undertand and model forest carbon dynamics, and have additional implications for theories of resource allocation and plant senescence.</p> </li> </ol> <div class="pull-right"> <ul class="pagination"> <li><a href="#" onclick='return showDiv("page_1");'>«</a></li> <li><a href="#" onclick='return showDiv("page_14");'>14</a></li> <li><a href="#" onclick='return showDiv("page_15");'>15</a></li> <li class="active"><span>16</span></li> <li><a href="#" onclick='return showDiv("page_17");'>17</a></li> <li><a href="#" onclick='return showDiv("page_18");'>18</a></li> <li><a href="#" onclick='return showDiv("page_25");'>»</a></li> </ul> </div> </div><!-- col-sm-12 --> </div><!-- row --> </div><!-- page_16 --> <div id="page_17" class="hiddenDiv"> <div class="row"> <div class="col-sm-12"> <div class="pull-right"> <ul class="pagination"> <li><a href="#" onclick='return showDiv("page_1");'>«</a></li> <li><a href="#" onclick='return showDiv("page_15");'>15</a></li> <li><a href="#" onclick='return showDiv("page_16");'>16</a></li> <li class="active"><span>17</span></li> <li><a href="#" onclick='return showDiv("page_18");'>18</a></li> <li><a href="#" onclick='return showDiv("page_19");'>19</a></li> <li><a href="#" onclick='return showDiv("page_25");'>»</a></li> </ul> </div> </div> </div> <div class="row"> <div class="col-sm-12"> <ol class="result-class" start="321"> <li> <p><a target="_blank" rel="noopener noreferrer" onclick="trackOutboundLink('http://adsabs.harvard.edu/abs/2016AGUFM.B23D0619M','NASAADS'); return false;" href="http://adsabs.harvard.edu/abs/2016AGUFM.B23D0619M"><span>Black carbon content in a ponderosa pine forest of eastern Oregon with varying seasons and intervals of prescribed burns</span></a></p> <p><a target="_blank" rel="noopener noreferrer" href="http://adsabs.harvard.edu/abstract_service.html">NASA Astrophysics Data System (ADS)</a></p> <p>Matosziuk, L.; Hatten, J. A.</p> <p>2016-12-01</p> <p>Soil carbon represents a significant component of the global carbon cycle. While fire-based disturbance of forest ecosystems acts as a carbon source, the increased temperatures can initiate molecular changes to forest biomass that convert fast cycling organic carbon into more stable forms such as black carbon (BC), a product of incomplete combustion that contains highly-condensed aromatic structures and very low hydrogen and oxygen content. Such forms of carbon can remain in the soil for hundred to thousands of years, effectively creating a long-term carbon sink. The goal of this project is to understand how specific characteristics of prescribed burns, specifically the season of burn and the interval between burns, affect the formation, structure, and retention of these slowly degrading forms of carbon in the soil. Both O-horizon (forest floor) and mineral soil (0-15 cm cores) samples were collected from a season and interval of burn study in Malheur National Forest. The study area is divided into six replicate units, each of which is sub-divided into four treatment areas and a control. Beginning in 1997, each treatment area was subjected to: i) spring burns at five-year intervals, ii) fall burns at five-year intervals, iii) spring burns at 15-year intervals, or iv) fall burns at 15-year intervals. The bulk density, pH, and C/N content of each soil were measured to assess the effect of the burn treatments on the soil. Additionally, the amount and molecular structure of BC in each sample was quantified using the distribution of specific molecular markers (benzene polycarboxylic acids or BPCAs) that are present in the soil following acid digestion.</p> </li> <li> <p><a target="_blank" rel="noopener noreferrer" onclick="trackOutboundLink('http://adsabs.harvard.edu/abs/2017JPS...362...64L','NASAADS'); return false;" href="http://adsabs.harvard.edu/abs/2017JPS...362...64L"><span>Rational construction of nickel cobalt sulfide nanoflakes on CoO nanosheets with the help of carbon layer as the battery-like electrode for supercapacitors</span></a></p> <p><a target="_blank" rel="noopener noreferrer" href="http://adsabs.harvard.edu/abstract_service.html">NASA Astrophysics Data System (ADS)</a></p> <p>Lin, Jinghuang; Liu, Yulin; Wang, Yiheng; Jia, Henan; Chen, Shulin; Qi, Junlei; Qu, Chaoqun; Cao, Jian; Fei, Weidong; Feng, Jicai</p> <p>2017-09-01</p> <p>Herein, binder-free hierarchically structured nickel cobalt sulfide nanoflakes on CoO nanosheets with the help of carbon layer (Ni-Co-S@C@CoO NAs) are fabricated via hydrothermal synthesis, carbonization treatment and electrodeposition, where three key components (CoO nanosheet arrays, a carbon layer and Ni-Co-S nanoflakes) are strategically combined to construct an efficient electrode for supercapacitors. The highly well-defined CoO nanosheets are utilized as ideal conductive scaffolds, where the conductivity is further improved by coating carbon layer, as well as the large electroactive surface area of Ni-Co-S nanoflakes. Furthermore, self-supported electrodes are directly grown on Ni foam without conductive additives or binders, which can effectively simplify the whole preparation process and achieve excellent electrical contact. Benefiting from the unique structural features, the hierarchically structured Ni-Co-S@C@CoO NAs exhibit high specific capacitance up to 4.97 F cm-2, excellent rate capability, and maintains 93.2% of the initial capacitance after 10000 cycles. Furthermore, an asymmetric supercapacitor using the Ni-Co-S@C@CoO NAs electrode and activated carbon is assembled, which achieves a high energy density (49.7 W h kg-1) with long cycling lifespan. These results demonstrate the as-fabricated Ni-Co-S@C@CoO NAs can be a competitive battery-like electrode for supercapacitors in energy storages.</p> </li> <li> <p><a target="_blank" rel="noopener noreferrer" onclick="trackOutboundLink('https://eric.ed.gov/?q=fossils&pg=2&id=EJ1024645','ERIC'); return false;" href="https://eric.ed.gov/?q=fossils&pg=2&id=EJ1024645"><span>Carbon Goes To…</span></a></p> <p><a target="_blank" rel="noopener noreferrer" href="http://www.eric.ed.gov/ERICWebPortal/search/extended.jsp?_pageLabel=advanced">ERIC Educational Resources Information Center</a></p> <p>Savasci, Funda</p> <p>2014-01-01</p> <p>The purposes of this activity are to help middle school students understand the carbon cycle and realize how human activities affect the carbon cycle. This activity consists of two parts. The first part of the activity focuses on the carbon cycle, especially before the Industrial Revolution, while the second part of the activity focuses on how…</p> </li> <li> <p><a target="_blank" rel="noopener noreferrer" onclick="trackOutboundLink('https://www.gpo.gov/fdsys/pkg/CFR-2012-title40-vol12/pdf/CFR-2012-title40-vol12-part63-subpartMMM-app3.pdf','CFR2012'); return false;" href="https://www.gpo.gov/fdsys/pkg/CFR-2012-title40-vol12/pdf/CFR-2012-title40-vol12-part63-subpartMMM-app3.pdf"><span>40 CFR Table 3 to Subpart Mmm of... - Monitoring Requirements for Control Devices a</span></a></p> <p><a target="_blank" rel="noopener noreferrer" href="http://www.gpo.gov/fdsys/browse/collectionCfr.action?selectedYearFrom=2012&page.go=Go">Code of Federal Regulations, 2012 CFR</a></p> <p></p> <p>2012-07-01</p> <p>.... Carbon adsorber (regenerative) Stream flow monitoring device, and 1. Total regeneration stream mass or volumetric flow during carbon bed regeneration cycle(s) 1. For each regeneration cycle, record the total regeneration stream mass or volumetric flow. Carbon bed temperature monitoring device 2. Temperature of carbon...</p> </li> <li> <p><a target="_blank" rel="noopener noreferrer" onclick="trackOutboundLink('https://www.gpo.gov/fdsys/pkg/CFR-2011-title40-vol11/pdf/CFR-2011-title40-vol11-part63-subpartMMM-app3.pdf','CFR2011'); return false;" href="https://www.gpo.gov/fdsys/pkg/CFR-2011-title40-vol11/pdf/CFR-2011-title40-vol11-part63-subpartMMM-app3.pdf"><span>40 CFR Table 3 to Subpart Mmm of... - Monitoring Requirements for Control Devices a</span></a></p> <p><a target="_blank" rel="noopener noreferrer" href="http://www.gpo.gov/fdsys/browse/collectionCfr.action?selectedYearFrom=2011&page.go=Go">Code of Federal Regulations, 2011 CFR</a></p> <p></p> <p>2011-07-01</p> <p>.... Carbon adsorber (regenerative) Stream flow monitoring device, and 1. Total regeneration stream mass or volumetric flow during carbon bed regeneration cycle(s) 1. For each regeneration cycle, record the total regeneration stream mass or volumetric flow. Carbon bed temperature monitoring device 2. Temperature of carbon...</p> </li> <li> <p><a target="_blank" rel="noopener noreferrer" onclick="trackOutboundLink('https://www.gpo.gov/fdsys/pkg/CFR-2010-title40-vol11/pdf/CFR-2010-title40-vol11-part63-subpartMMM-app3.pdf','CFR'); return false;" href="https://www.gpo.gov/fdsys/pkg/CFR-2010-title40-vol11/pdf/CFR-2010-title40-vol11-part63-subpartMMM-app3.pdf"><span>40 CFR Table 3 to Subpart Mmm of... - Monitoring Requirements for Control Devices a</span></a></p> <p><a target="_blank" rel="noopener noreferrer" href="http://www.gpo.gov/fdsys/browse/collectionCfr.action?selectedYearFrom=2010&page.go=Go">Code of Federal Regulations, 2010 CFR</a></p> <p></p> <p>2010-07-01</p> <p>.... Carbon adsorber (regenerative) Stream flow monitoring device, and 1. Total regeneration stream mass or volumetric flow during carbon bed regeneration cycle(s) 1. For each regeneration cycle, record the total regeneration stream mass or volumetric flow. Carbon bed temperature monitoring device 2. Temperature of carbon...</p> </li> <li> <p><a target="_blank" rel="noopener noreferrer" onclick="trackOutboundLink('https://www.ncbi.nlm.nih.gov/pubmed/28570016','PUBMED'); return false;" href="https://www.ncbi.nlm.nih.gov/pubmed/28570016"><span>Divergent taxonomic and functional responses of microbial communities to field simulation of aeolian soil erosion and deposition.</span></a></p> <p><a target="_blank" rel="noopener noreferrer" href="https://www.ncbi.nlm.nih.gov/entrez/query.fcgi?DB=pubmed">PubMed</a></p> <p>Ma, Xingyu; Zhao, Cancan; Gao, Ying; Liu, Bin; Wang, Tengxu; Yuan, Tong; Hale, Lauren; Nostrand, Joy D Van; Wan, Shiqiang; Zhou, Jizhong; Yang, Yunfeng</p> <p>2017-08-01</p> <p>Aeolian soil erosion and deposition have worldwide impacts on agriculture, air quality and public health. However, ecosystem responses to soil erosion and deposition remain largely unclear in regard to microorganisms, which are the crucial drivers of biogeochemical cycles. Using integrated metagenomics technologies, we analysed microbial communities subjected to simulated soil erosion and deposition in a semiarid grassland of Inner Mongolia, China. As expected, soil total organic carbon and plant coverage were decreased by soil erosion, and soil dissolved organic carbon (DOC) was increased by soil deposition, demonstrating that field simulation was reliable. Soil microbial communities were altered (p < .039) by both soil erosion and deposition, with dramatic increase in Cyanobacteria related to increased stability in soil aggregates. amyA genes encoding α-amylases were specifically increased (p = .01) by soil deposition and positively correlated (p = .02) to DOC, which likely explained changes in DOC. Surprisingly, most of microbial functional genes associated with carbon, nitrogen, phosphorus and potassium cycling were decreased or unaltered by both erosion and deposition, probably arising from acceleration of organic matter mineralization. These divergent responses support the necessity to include microbial components in evaluating ecological consequences. Furthermore, Mantel tests showed strong, significant correlations between soil nutrients and functional structure but not taxonomic structure, demonstrating close relevance of microbial function traits to nutrient cycling. © 2017 John Wiley & Sons Ltd.</p> </li> <li> <p><a target="_blank" rel="noopener noreferrer" onclick="trackOutboundLink('https://www.osti.gov/servlets/purl/881063','SCIGOV-STC'); return false;" href="https://www.osti.gov/servlets/purl/881063"><span>Young organic matter as a source of carbon dioxide outgassing from Amazonian rivers</span></a></p> <p><a target="_blank" rel="noopener noreferrer" href="http://www.osti.gov/search">DOE Office of Scientific and Technical Information (OSTI.GOV)</a></p> <p>Mayorga, E; Aufdenkampe, A K; Masiello, C A</p> <p>2005-06-23</p> <p>Rivers are generally supersaturated with respect to carbon dioxide, resulting in large gas evasion fluxes that can be a significant component of regional net carbon budgets. Amazonian rivers were recently shown to outgas more than ten times the amount of carbon exported to the ocean in the form of total organic carbon or dissolved inorganic carbon. High carbon dioxide concentrations in rivers originate largely from in situ respiration of organic carbon, but little agreement exists about the sources or turnover times of this carbon. Here we present results of an extensive survey of the carbon isotope composition ({sup 13}C andmore » {sup 14}C) of dissolved inorganic carbon and three size-fractions of organic carbon across the Amazonian river system. We find that respiration of contemporary organic matter (less than 5 years old) originating on land and near rivers is the dominant source of excess carbon dioxide that drives outgassing in mid-size to large rivers, although we find that bulk organic carbon fractions transported by these rivers range from tens to thousands of years in age. We therefore suggest that a small, rapidly cycling pool of organic carbon is responsible for the large carbon fluxes from land to water to atmosphere in the humid tropics.« less</p> </li> <li> <p><a target="_blank" rel="noopener noreferrer" onclick="trackOutboundLink('http://adsabs.harvard.edu/abs/2015Nanos...7.3270Z','NASAADS'); return false;" href="http://adsabs.harvard.edu/abs/2015Nanos...7.3270Z"><span>Encapsulation of α-Fe2O3 nanoparticles in graphitic carbon microspheres as high-performance anode materials for lithium-ion batteries</span></a></p> <p><a target="_blank" rel="noopener noreferrer" href="http://adsabs.harvard.edu/abstract_service.html">NASA Astrophysics Data System (ADS)</a></p> <p>Zhang, Hongwei; Sun, Xiaoran; Huang, Xiaodan; Zhou, Liang</p> <p>2015-02-01</p> <p>A novel ``spray drying-carbonization-oxidation'' strategy has been developed for the fabrication of α-Fe2O3-graphitic carbon (α-Fe2O3@GC) composite microspheres, in which α-Fe2O3 nanoparticles with sizes of 30-50 nm are well-encapsulated by onion-like graphitic carbon shells with a thickness of 5-10 nm. In the constructed composite, the α-Fe2O3 nanoparticles act as the primary active material, providing a high capacity. Meanwhile, the graphitic carbon shells serve as the secondary active component, structural stabilizer, interfacial stabilizer, and electron-highway. As a result, the synthesized α-Fe2O3@GC nanocomposite exhibits a superior lithium-ion battery performance with a high reversible capacity (898 mA h g-1 at 400 mA g-1), outstanding rate capability, and excellent cycling stability. Our product, in terms of the facile and scalable preparation process and excellent electrochemical performance, demonstrates its great potential as a high-performance anode material for lithium-ion batteries.A novel ``spray drying-carbonization-oxidation'' strategy has been developed for the fabrication of α-Fe2O3-graphitic carbon (α-Fe2O3@GC) composite microspheres, in which α-Fe2O3 nanoparticles with sizes of 30-50 nm are well-encapsulated by onion-like graphitic carbon shells with a thickness of 5-10 nm. In the constructed composite, the α-Fe2O3 nanoparticles act as the primary active material, providing a high capacity. Meanwhile, the graphitic carbon shells serve as the secondary active component, structural stabilizer, interfacial stabilizer, and electron-highway. As a result, the synthesized α-Fe2O3@GC nanocomposite exhibits a superior lithium-ion battery performance with a high reversible capacity (898 mA h g-1 at 400 mA g-1), outstanding rate capability, and excellent cycling stability. Our product, in terms of the facile and scalable preparation process and excellent electrochemical performance, demonstrates its great potential as a high-performance anode material for lithium-ion batteries. Electronic supplementary information (ESI) available: XRD pattern, XPS spectrum, CV curves, TEM and SEM images, and table. See DOI: 10.1039/c4nr06771a</p> </li> <li> <p><a target="_blank" rel="noopener noreferrer" onclick="trackOutboundLink('https://www.ncbi.nlm.nih.gov/pubmed/22919856','PUBMED'); return false;" href="https://www.ncbi.nlm.nih.gov/pubmed/22919856"><span>[Roles of soil dissolved organic carbon in carbon cycling of terrestrial ecosystems: a review].</span></a></p> <p><a target="_blank" rel="noopener noreferrer" href="https://www.ncbi.nlm.nih.gov/entrez/query.fcgi?DB=pubmed">PubMed</a></p> <p>Li, Ling; Qiu, Shao-Jun; Liu, Jing-Tao; Liu, Qing; Lu, Zhao-Hua</p> <p>2012-05-01</p> <p>Soil dissolved organic carbon (DOC) is an active fraction of soil organic carbon pool, playing an important role in the carbon cycling of terrestrial ecosystems. In view of the importance of the carbon cycling, this paper summarized the roles of soil DOC in the soil carbon sequestration and greenhouse gases emission, and in considering of our present ecological and environmental problems such as soil acidification and climate warming, discussed the effects of soil properties, environmental factors, and human activities on the soil DOC as well as the response mechanisms of the DOC. This review could be helpful to the further understanding of the importance of soil DOC in the carbon cycling of terrestrial ecosystems and the reduction of greenhouse gases emission.</p> </li> <li> <p><a target="_blank" rel="noopener noreferrer" onclick="trackOutboundLink('http://adsabs.harvard.edu/abs/2012BGD.....9.1097A','NASAADS'); return false;" href="http://adsabs.harvard.edu/abs/2012BGD.....9.1097A"><span>The contribution of respiration in tree-stems to the Dole Effect</span></a></p> <p><a target="_blank" rel="noopener noreferrer" href="http://adsabs.harvard.edu/abstract_service.html">NASA Astrophysics Data System (ADS)</a></p> <p>Angert, A.; Muhr, J.; Negron Juarez, R.; Alegria Muñoz, W.; Kraemer, G.; Ramirez Santillan, J.; Chambers, J. Q.; Trumbore, S. E.</p> <p>2012-01-01</p> <p>Understanding the variability and the current value of the Dole Effect, which has been used to infer past changes in biospheric productivity, requires accurate information on the discrimination associated with respiratory oxygen consumption in each of the biosphere components. Respiration in tree stems is an important component of the land carbon cycle. Here we measured, for the first time, the discrimination associated with tree stem oxygen uptake. The measurements included tropical forest trees, which are major contributors to the global fluxes of carbon and oxygen. We found discrimination in the range of 12.6-21.5 ‰, indicating both diffusion limitation, resulting in O2 discrimination values below 20 ‰, and alternative oxidase respiration, which resulted in discrimination values greater than 20 ‰. Discrimination varied seasonally, between and within tree species. Calculations based on these results show that variability in woody plants discrimination can result in significant variations in the global Dole Effect.</p> </li> <li> <p><a target="_blank" rel="noopener noreferrer" onclick="trackOutboundLink('http://adsabs.harvard.edu/abs/2012BGeo....9.4037A','NASAADS'); return false;" href="http://adsabs.harvard.edu/abs/2012BGeo....9.4037A"><span>The contribution of respiration in tree stems to the Dole Effect</span></a></p> <p><a target="_blank" rel="noopener noreferrer" href="http://adsabs.harvard.edu/abstract_service.html">NASA Astrophysics Data System (ADS)</a></p> <p>Angert, A.; Muhr, J.; Negron Juarez, R.; Alegria Muñoz, W.; Kraemer, G.; Ramirez Santillan, J.; Chambers, J. Q.; Trumbore, S. E.</p> <p>2012-10-01</p> <p>Understanding the variability and the current value of the Dole Effect, which has been used to infer past changes in biospheric productivity, requires accurate information on the isotopic discrimination associated with respiratory oxygen consumption in each of the biosphere components. Respiration in tree stems is an important component of the land carbon cycle. Here we measured, for the first time, the discrimination associated with tree stem oxygen uptake. The measurements included tropical forest trees, which are major contributors to the global fluxes of carbon and oxygen. We found discrimination in the range of 12.6-21.5‰, indicating both diffusion limitation, resulting in O2 discrimination values below 20‰, and alternative oxidase respiration, which resulted in discrimination values greater than 20‰. Discrimination varied seasonally, between and within tree species. Calculations based on these results show that variability in woody plants discrimination can result in significant variations in the global Dole Effect.</p> </li> <li> <p><a target="_blank" rel="noopener noreferrer" onclick="trackOutboundLink('https://ntrs.nasa.gov/search.jsp?R=20050203865&hterms=carbon&qs=Ntx%3Dmode%2Bmatchall%26Ntk%3DTitle%26N%3D0%26No%3D90%26Ntt%3Dcarbon','NASA-TRS'); return false;" href="https://ntrs.nasa.gov/search.jsp?R=20050203865&hterms=carbon&qs=Ntx%3Dmode%2Bmatchall%26Ntk%3DTitle%26N%3D0%26No%3D90%26Ntt%3Dcarbon"><span>Carbon-Carbon Recuperators in Closed-Brayton-Cycle Nuclear Space Power Systems: A Feasibility Assessment</span></a></p> <p><a target="_blank" rel="noopener noreferrer" href="http://ntrs.nasa.gov/search.jsp">NASA Technical Reports Server (NTRS)</a></p> <p>Barrett, Michael J.; Johnson, Paul K.</p> <p>2004-01-01</p> <p>The feasibility of using carbon-carbon recuperators in closed-Brayton-cycle (CBC) nuclear space power conversion systems (PCS) was assessed. Recuperator performance expectations were forecast based on projected thermodynamic cycle state values for a planetary mission. Resulting thermal performance, mass and volume for a plate-fin carbon-carbon recuperator were estimated and quantitatively compared with values for a conventional offset-strip-fin metallic design. Material compatibility issues regarding carbon-carbon surfaces exposed to the working fluid in the CBC PCS were also discussed.</p> </li> <li> <p><a target="_blank" rel="noopener noreferrer" onclick="trackOutboundLink('http://hdl.handle.net/2060/20180000620','NASA-TRS'); return false;" href="http://hdl.handle.net/2060/20180000620"><span>The 2015-2016 El Nino and the Response of the Carbon Cycle: Findings from NASA's OCO-2 Mission</span></a></p> <p><a target="_blank" rel="noopener noreferrer" href="http://ntrs.nasa.gov/search.jsp">NASA Technical Reports Server (NTRS)</a></p> <p>Chatterjee, Abhishek; Schimel, D.; Stephens, B.; Crisp, D.; Eldering, A.; Feely, R.; Gierach, M.; Gunson, M.; Keeling, R.; Landschuetzer, P.; <a style="text-decoration: none; " href="javascript:void(0); " onClick="displayelement('author_20180000620'); toggleEditAbsImage('author_20180000620_show'); toggleEditAbsImage('author_20180000620_hide'); "> <img style="display:inline; width:12px; height:12px; " src="images/arrow-up.gif" width="12" height="12" border="0" alt="hide" id="author_20180000620_show"> <img style="width:12px; height:12px; display:none; " src="images/arrow-down.gif" width="12" height="12" border="0" alt="hide" id="author_20180000620_hide"></p> <p>2017-01-01</p> <p>The El Nino Southern Oscillation (ENSO) is the most important mode of tropical climate variability on interannual to decadal time scales. Correlations between atmospheric CO2 growth rate and ENSO activity are relatively well known but the magnitude of this correlation, the contribution from tropical marine vs. terrestrial flux components, and the causal mechanisms, are poorly constrained in space and time. The launch of NASA's Orbiting Carbon Observatory-2 (OCO-2) mission in July 2014 was rather timely given the development of strong ENSO conditions over the tropical Pacific Ocean in 2015-2016. In this presentation, we will discuss how the high-density observations from OCO-2 provided us with a novel dataset to resolve the linkages between El Nino and atmospheric CO2. Along with information from in situ observations of ÎpCO2 from NOAA's Tropical Atmosphere Ocean (TAO) project and atmospheric CO2 from the Scripps CO2 Program, and other remote-sensing missions, we are able to piece together the time dependent response of atmospheric CO2 concentrations over the Tropics. Our findings confirm the hypothesis from studies following the 1997-1998 El Nino event that an early reduction in CO2 outgassing from the tropical Pacific Ocean is later reversed by enhanced net CO2 emissions from the terrestrial biosphere. This implies that a component of the interannual variability (IAV) in the growth rate of atmospheric CO2, which has typically been used to constrain the climate sensitivity of tropical land carbon fluxes, is strongly influenced and modified by ocean fluxes during the early phase of the ENSO event. Our analyses shed further light on the understanding of the marine vs. terrestrial partitioning of tropical carbon fluxes during El Nino events, their relative contributions to the global atmospheric CO2 growth rate, and provide clues about the sensitivity of the carbon cycle to climate forcing on interannual time scales.</p> </li> <li> <p><a target="_blank" rel="noopener noreferrer" onclick="trackOutboundLink('http://hdl.handle.net/2060/19950022627','NASA-TRS'); return false;" href="http://hdl.handle.net/2060/19950022627"><span>Effects of thermal and moisture cycling on the internal structure of stitched RTM laminates</span></a></p> <p><a target="_blank" rel="noopener noreferrer" href="http://ntrs.nasa.gov/search.jsp">NASA Technical Reports Server (NTRS)</a></p> <p>Walker, Jeff; Roundy, Lance; Goering, Jon</p> <p>1993-01-01</p> <p>Conventional aerospace composites are strong and stiff in the directions parallel to the carbon fibers, but they are prone to delaminations and damage in the through-the-thickness directions. Recent research has shown that substantial improvements in damage tolerance are obtained from textile composites with Z-direction reinforcement provided by stitching, weaving, or braiding. Because of the mismatch in thermal and moisture expansion properties of the various material components, there is a potential for microcracks to develop in the resin matrix. These cracks can form to relieve the mechanical stresses that are generated during curing or in-service temperature cycles.</p> </li> <li> <p><a target="_blank" rel="noopener noreferrer" onclick="trackOutboundLink('http://adsabs.harvard.edu/abs/2017AGUFMOS31D..08G','NASAADS'); return false;" href="http://adsabs.harvard.edu/abs/2017AGUFMOS31D..08G"><span>The Influence of Submarine Groundwater Discharge on Nearshore Marine Dissolved Organic Carbon Reactivity, Concentration Dynamics, and Offshore Export</span></a></p> <p><a target="_blank" rel="noopener noreferrer" href="http://adsabs.harvard.edu/abstract_service.html">NASA Astrophysics Data System (ADS)</a></p> <p>Goodridge, B.</p> <p>2017-12-01</p> <p>Dissolved organic carbon (DOC) is the largest pool of reduced carbon in the oceans, with a reservoir equivalent to atmospheric CO2. In nearshore marine regions, DOC sources include primary production, terrestrial DOC delivered by river discharge, and/or terrestrial and marine DOC delivered via submarine groundwater discharge (SGD). While the importance of SGD to coastal carbon cycling has been implicated, the actual influence of this process on nearshore carbon dynamics and offshore export has not been explicitly identified. This study, conducted at a predominantly marine-influenced intertidal beach-nearshore ocean system along the Santa Barbara, California coastline, aimed to address this knowledge gap. I coupled dark, temperature-controlled laboratory incubations, radioisotopic (Rn-222) SGD estimates, and a DOC box model to identify the influence of pore water mixing with seawater on nearshore DOC reactivity, concentration dynamics, and offshore export. Even with a relatively low volumetric contribution, SGD pore water mixing altered nearshore DOC reactivity, and elevated the nearshore DOC concentration by 0.9 to 5.6 µmol L-1 over nearshore seawater residence times ranging from 1 to 6 days. These elevated DOC concentrations were equivalent to 1.2 to 7.5% of the mean offshore DOC concentration taken during the summer months in the Santa Barbara Channel, when the coastal water column is highly thermally stratified. Despite the challenge of assessing carbon dynamics in physically and biogeochemically complex nearshore marine regions, this study demonstrates the need for future investigations to assess and account for SGD as a non-trivial component of coastal marine carbon cycles.</p> </li> <li> <p><a target="_blank" rel="noopener noreferrer" onclick="trackOutboundLink('https://ntrs.nasa.gov/search.jsp?R=20130009354&hterms=fourier&qs=Ntx%3Dmode%2Bmatchall%26Ntk%3DAll%26N%3D0%26No%3D10%26Ntt%3Dfourier','NASA-TRS'); return false;" href="https://ntrs.nasa.gov/search.jsp?R=20130009354&hterms=fourier&qs=Ntx%3Dmode%2Bmatchall%26Ntk%3DAll%26N%3D0%26No%3D10%26Ntt%3Dfourier"><span>The Geostationary Fourier Transform Spectrometer</span></a></p> <p><a target="_blank" rel="noopener noreferrer" href="http://ntrs.nasa.gov/search.jsp">NASA Technical Reports Server (NTRS)</a></p> <p>Key, Richard; Sander, Stanley; Eldering, Annmarie; Blavier, Jean-Francois; Bekker, Dmitriy; Manatt, Ken; Rider, David; Wu, Yen-Hung</p> <p>2012-01-01</p> <p>The Geostationary Fourier Transform Spectrometer (GeoFTS) is an imaging spectrometer designed for a geostationary orbit (GEO) earth science mission to measure key atmospheric trace gases and process tracers related to climate change and human activity. GEO allows GeoFTS to continuously stare at a region of the earth for frequent sampling to capture the variability of biogenic fluxes and anthropogenic emissions from city to continental spatial scales and temporal scales from diurnal, synoptic, seasonal to interannual. The measurement strategy provides a process based understanding of the carbon cycle from contiguous maps of carbon dioxide (CO2), methane (CH4), carbon monoxide (CO), and chlorophyll fluorescence (CF) collected many times per day at high spatial resolution (2.7kmx2.7km at nadir). The CO2/CH4/CO/CF measurement suite in the near infrared spectral region provides the information needed to disentangle natural and anthropogenic contributions to atmospheric carbon concentrations and to minimize uncertainties in the flow of carbon between the atmosphere and surface. The half meter cube size GeoFTS instrument is based on a Michelson interferometer design that uses all high TRL components in a modular configuration to reduce complexity and cost. It is self-contained and as independent of the spacecraft as possible with simple spacecraft interfaces, making it ideal to be a "hosted" payload on a commercial communications satellite mission. The hosted payload approach for measuring the major carbon-containing gases in the atmosphere from the geostationary vantage point will affordably advance the scientific understating of carbon cycle processes and climate change.</p> </li> <li> <p><a target="_blank" rel="noopener noreferrer" onclick="trackOutboundLink('http://adsabs.harvard.edu/abs/2004PhST..111..199S','NASAADS'); return false;" href="http://adsabs.harvard.edu/abs/2004PhST..111..199S"><span>Flat Tile Armour Cooled by Hypervapotron Tube: a Possible Technology for ITER</span></a></p> <p><a target="_blank" rel="noopener noreferrer" href="http://adsabs.harvard.edu/abstract_service.html">NASA Astrophysics Data System (ADS)</a></p> <p>Schlosser, J.; Escourbiac, F.; Merola, M.; Schedler, B.; Bayetti, P.; Missirlian, M.; Mitteau, R.; Robin-Vastra, I.</p> <p></p> <p>Carbon fibre composite (CFC) flat tile armours for actively cooled plasma facing components (PFC’s) are an important challenge for controlled fusion machines. Flat tile concepts, water cooled by tubes, were studied, developed, tested and finally operated with success in Tore Supra. The components were designed for 10 MW/m2 and mock-ups were successfully fatigue tested at 15 MW/m2, 1000 cycles. For ITER, a tube-in-tile concept was developed and mock-ups sustained up to 25 MW/m2 for 1000 cycles without failure. Recently flat tile armoured mock-ups cooled by a hypervapotron tube successfully sustained a cascade failure test under a mean heat flux of 10 MW/m2 but with a doubling of the heat flux on some tiles to simulate missing tiles (500 cycles). This encouraging results lead to reconsider the limits for flat tile concept when cooled by hypervapotron (HV) tube. New tests are now scheduled to investigate these limits in regard to the ITER requirements. Experimental evidence of the concept could be gained in Tore Supra by installing a new limiter into the machine.</p> </li> <li> <p><a target="_blank" rel="noopener noreferrer" onclick="trackOutboundLink('https://www.fs.usda.gov/treesearch/pubs/55224','TREESEARCH'); return false;" href="https://www.fs.usda.gov/treesearch/pubs/55224"><span>Genetic bases of fungal white rot wood decay predicted by phylogenomic analysis of correlated gene-phenotype evolution</span></a></p> <p><a target="_blank" rel="noopener noreferrer" href="http://www.fs.usda.gov/treesearch/">Treesearch</a></p> <p>László G. Nagy; Robert Riley; Philip J. Bergmann; Krisztina Krizsán; Francis M. Martin; Igor V. Grigoriev; Dan Cullen; David S. Hibbett</p> <p>2016-01-01</p> <p>Fungal decomposition of plant cell walls (PCW) is a complex process that has diverse industrial applications and huge impacts on the carbon cycle. White rot (WR) is a powerful mode of PCW decay in which lignin and carbohydrates are both degraded. Mechanistic studies of decay coupled with comparative genomic analyses have provided clues to the enzymatic components of WR...</p> </li> <li> <p><a target="_blank" rel="noopener noreferrer" onclick="trackOutboundLink('https://www.gpo.gov/fdsys/pkg/CFR-2013-title40-vol12/pdf/CFR-2013-title40-vol12-part63-subpartMMM-app3.pdf','CFR2013'); return false;" href="https://www.gpo.gov/fdsys/pkg/CFR-2013-title40-vol12/pdf/CFR-2013-title40-vol12-part63-subpartMMM-app3.pdf"><span>40 CFR Table 3 to Subpart Mmm of... - Monitoring Requirements for Control Devices a</span></a></p> <p><a target="_blank" rel="noopener noreferrer" href="http://www.gpo.gov/fdsys/browse/collectionCfr.action?selectedYearFrom=2013&page.go=Go">Code of Federal Regulations, 2013 CFR</a></p> <p></p> <p>2013-07-01</p> <p>... regeneration stream mass or volumetric flow during carbon bed regeneration cycle(s) 1. For each regeneration cycle, record the total regeneration stream mass or volumetric flow. Carbon bed temperature monitoring device 2. Temperature of carbon bed after regeneration 2. For each regeneration cycle, record the maximum...</p> </li> </ol> <div class="pull-right"> <ul class="pagination"> <li><a href="#" onclick='return showDiv("page_1");'>«</a></li> <li><a href="#" onclick='return showDiv("page_15");'>15</a></li> <li><a href="#" onclick='return showDiv("page_16");'>16</a></li> <li class="active"><span>17</span></li> <li><a href="#" onclick='return showDiv("page_18");'>18</a></li> <li><a href="#" onclick='return showDiv("page_19");'>19</a></li> <li><a href="#" onclick='return showDiv("page_25");'>»</a></li> </ul> </div> </div><!-- col-sm-12 --> </div><!-- row --> </div><!-- page_17 --> <div id="page_18" class="hiddenDiv"> <div class="row"> <div class="col-sm-12"> <div class="pull-right"> <ul class="pagination"> <li><a href="#" onclick='return showDiv("page_1");'>«</a></li> <li><a href="#" onclick='return showDiv("page_16");'>16</a></li> <li><a href="#" onclick='return showDiv("page_17");'>17</a></li> <li class="active"><span>18</span></li> <li><a href="#" onclick='return showDiv("page_19");'>19</a></li> <li><a href="#" onclick='return showDiv("page_20");'>20</a></li> <li><a href="#" onclick='return showDiv("page_25");'>»</a></li> </ul> </div> </div> </div> <div class="row"> <div class="col-sm-12"> <ol class="result-class" start="341"> <li> <p><a target="_blank" rel="noopener noreferrer" onclick="trackOutboundLink('https://www.gpo.gov/fdsys/pkg/CFR-2014-title40-vol12/pdf/CFR-2014-title40-vol12-part63-subpartMMM-app3.pdf','CFR2014'); return false;" href="https://www.gpo.gov/fdsys/pkg/CFR-2014-title40-vol12/pdf/CFR-2014-title40-vol12-part63-subpartMMM-app3.pdf"><span>40 CFR Table 3 to Subpart Mmm of... - Monitoring Requirements for Control Devices a</span></a></p> <p><a target="_blank" rel="noopener noreferrer" href="http://www.gpo.gov/fdsys/browse/collectionCfr.action?selectedYearFrom=2014&page.go=Go">Code of Federal Regulations, 2014 CFR</a></p> <p></p> <p>2014-07-01</p> <p>... regeneration stream mass or volumetric flow during carbon bed regeneration cycle(s) 1. For each regeneration cycle, record the total regeneration stream mass or volumetric flow. Carbon bed temperature monitoring device 2. Temperature of carbon bed after regeneration 2. For each regeneration cycle, record the maximum...</p> </li> <li> <p><a target="_blank" rel="noopener noreferrer" onclick="trackOutboundLink('http://adsabs.harvard.edu/abs/2014AGUFMPP23D..06L','NASAADS'); return false;" href="http://adsabs.harvard.edu/abs/2014AGUFMPP23D..06L"><span>Late Pleistocene Magnitude Glacial Incursions of Southern Component Water to the Deep North Atlantic Resolved Using Nd Isotopes during the Intensification of Northern Hemisphere Glaciation (3.3 to 2.4 Ma)</span></a></p> <p><a target="_blank" rel="noopener noreferrer" href="http://adsabs.harvard.edu/abstract_service.html">NASA Astrophysics Data System (ADS)</a></p> <p>Lang, D.; Bailey, I.; Wilson, P. A.; Foster, G. L.; Gutjahr, M.</p> <p>2014-12-01</p> <p>The ocean, through its ability to globally redistribute heat and partition carbon dioxide, is believed to play a key role in driving and amplifying climate change during Quaternary glaciations on orbital to millennial timescales. Relatively little is known, however, about changes in Atlantic Meridional Overturning Circulation (AMOC) associated with the Pliocene intensification of Northern Hemisphere glaciation (iNHG). To help fill this gap in our knowledge we present a new high resolution (~6 ka) record of the Nd isotope composition of the deep North Atlantic between ~3.3 and 2.4 Ma, measured on fish debris at IODP Site U1313 (3426 m, 41°N, 32.5°W). This record represents the first orbital-resolution record of variations in watermass mixing in this region for iNHG independent of changes in the carbon cycle and, in contrast to existing benthic foraminiferal δ13C records for this time interval, our Nd dataset contains evidence for late Pleistocene magnitude incursions of Southern Component Waters to the deep North Atlantic Ocean during key glacial periods through this time. We therefore infer an important role for AMOC variability in amplifying Quaternary glacial-interglacial cycles</p> </li> <li> <p><a target="_blank" rel="noopener noreferrer" onclick="trackOutboundLink('https://pubs.er.usgs.gov/publication/70021147','USGSPUBS'); return false;" href="https://pubs.er.usgs.gov/publication/70021147"><span>Effects of a clear-cut harvest on soil respiration in a jack pine - Lichen woodland</span></a></p> <p><a target="_blank" rel="noopener noreferrer" href="http://pubs.er.usgs.gov/pubs/index.jsp?view=adv">USGS Publications Warehouse</a></p> <p>Striegl, Robert G.; Wickland, K.P.</p> <p>1998-01-01</p> <p>Quantification of the components of ecosystem respiration is essential to understanding carbon (C) cycling of natural and disturbed landscapes. Soil respiration, which includes autotrophic and heterotrophic respiration from throughout the soil profile, is the second largest flux in the global carbon cycle. We measured soil respiration (soil CO2 emission) at an undisturbed mature jack pine (Pinus banksiana Lamb.) stand in Saskatchewan (old jack pine, OJP), and at a formerly continuous portion of the stand that was clear-cut during the previous winter (clear-cut, CC). Tree harvesting reduced soil CO2 emission from ???22.5 to ???9.1 mol CO2??m2 for the 1994 growing season. OJP was a small net sink of atmospheric CO2, while CC was a net source of CO2. Winter emissions were similar at both sites. Reduction of soil respiration was attributed to disruption of the soil surface and to the death of tree roots. Flux simulations for CC and OJP identify 40% of CO2 emission at the undisturbed OJP site as near-surface respiration, 25% as deep-soil respiration, and 35% as tree-root respiration. The near-surface component was larger than the estimated annual C input to soil, suggesting fast C turnover and no net C accumulation in these boreal uplands in 1994.</p> </li> <li> <p><a target="_blank" rel="noopener noreferrer" onclick="trackOutboundLink('http://adsabs.harvard.edu/abs/2017AGUFM.B51B1789D','NASAADS'); return false;" href="http://adsabs.harvard.edu/abs/2017AGUFM.B51B1789D"><span>Matrix approaches to assess terrestrial nitrogen scheme in CLM4.5</span></a></p> <p><a target="_blank" rel="noopener noreferrer" href="http://adsabs.harvard.edu/abstract_service.html">NASA Astrophysics Data System (ADS)</a></p> <p>Du, Z.</p> <p>2017-12-01</p> <p>Terrestrial carbon (C) and nitrogen (N) cycles have been commonly represented by a series of balance equations to track their influxes into and effluxes out of individual pools in earth system models (ESMs). This representation matches our understanding of C and N cycle processes well but makes it difficult to track model behaviors. To overcome these challenges, we developed a matrix approach, which reorganizes the series of terrestrial C and N balance equations in the CLM4.5 into two matrix equations based on original representation of C and N cycle processes and mechanisms. The matrix approach would consequently help improve the comparability of models and data, evaluate impacts of additional model components, facilitate benchmark analyses, model intercomparisons, and data-model fusion, and improve model predictive power.</p> </li> <li> <p><a target="_blank" rel="noopener noreferrer" onclick="trackOutboundLink('https://www.ncbi.nlm.nih.gov/pubmed/26077391','PUBMED'); return false;" href="https://www.ncbi.nlm.nih.gov/pubmed/26077391"><span>Template synthesis of hollow MoS2-carbon nanocomposites using microporous organic polymers and their lithium storage properties.</span></a></p> <p><a target="_blank" rel="noopener noreferrer" href="https://www.ncbi.nlm.nih.gov/entrez/query.fcgi?DB=pubmed">PubMed</a></p> <p>Jin, Jaewon; Kim, Bolyong; Kim, Mincheol; Park, Nojin; Kang, Sungah; Lee, Sang Moon; Kim, Hae Jin; Son, Seung Uk</p> <p>2015-07-14</p> <p>This work shows that hollow and microporous organic polymers (H-MOPs) are good templating materials for the synthesis of inorganic material-carbon nanocomposites. The precursor compound, (NH4)2MoS4, was incorporated into H-MOPs. Heat treatment under argon resulted in the formation of hollow MoS2-carbon nanocomposites (MSC). According to microscopic analysis, the MoS2 in the MSC has a layered structure with an elongated interlayer distance. The MSC showed high reversible discharge capacities up to 802 mA h g(-1) after 30 cycles and excellent rate performance for lithium ion batteries. The promising electrochemical performance of the MSC is attributed to the very thin and disordered nature of MoS2 in the carbon skeleton. The role of chemical components of the MSC in the electrochemical process was suggested.</p> </li> <li> <p><a target="_blank" rel="noopener noreferrer" onclick="trackOutboundLink('http://www.osti.gov/sciencecinema/biblio/1015170','SCIGOVIMAGE-SCICINEMA'); return false;" href="http://www.osti.gov/sciencecinema/biblio/1015170"><span>Geologic Carbon Sequestration and Biosequestration (Carbon Cycle 2.0)</span></a></p> <p><a target="_blank" rel="noopener noreferrer" href="http://www.osti.gov/sciencecinema/">ScienceCinema</a></p> <p>DePaolo, Don</p> <p>2018-05-02</p> <p>Don DePaolo, Director of LBNL's Earth Sciences Division, speaks at the Carbon Cycle 2.0 kick-off symposium Feb. 3, 2010. We emit more carbon into the atmosphere than natural processes are able to remove - an imbalance with negative consequences. Carbon Cycle 2.0 is a Berkeley Lab initiative to provide the science needed to restore this balance by integrating the Labs diverse research activities and delivering creative solutions toward a carbon-neutral energy future.</p> </li> <li> <p><a target="_blank" rel="noopener noreferrer" onclick="trackOutboundLink('https://www.ncbi.nlm.nih.gov/pubmed/26953077','PUBMED'); return false;" href="https://www.ncbi.nlm.nih.gov/pubmed/26953077"><span>Delta-proteobacterial SAR324 group in hydrothermal plumes on the South Mid-Atlantic Ridge.</span></a></p> <p><a target="_blank" rel="noopener noreferrer" href="https://www.ncbi.nlm.nih.gov/entrez/query.fcgi?DB=pubmed">PubMed</a></p> <p>Cao, Huiluo; Dong, Chunming; Bougouffa, Salim; Li, Jiangtao; Zhang, Weipeng; Shao, Zongze; Bajic, Vladimir B; Qian, Pei-Yuan</p> <p>2016-03-08</p> <p>In the dark ocean, the SAR324 group of Delta-proteobacteria has been associated with a chemolithotrophic lifestyle. However, their electron transport chain for energy generation and information system has not yet been well characterized. In the present study, four SAR324 draft genomes were extracted from metagenomes sampled from hydrothermal plumes in the South Mid-Atlantic Ridge. We describe novel electron transport chain components in the SAR324 group, particularly the alternative complex III, which is involved in energy generation. Moreover, we propose that the C-type cytochrome, for example the C553, may play a novel role in electron transfer, adding to our knowledge regarding the energy generation process in the SAR324 cluster. The central carbon metabolism in the described SAR324 genomes exhibits several new features other than methanotrophy e.g. aromatic compound degradation. This suggests that methane oxidation may not be the main central carbon metabolism component in SAR324 cluster bacteria. The reductive acetyl-CoA pathway may potentially be essential in carbon fixation due to the absence of components from the Calvin-Benson cycle. Our study provides insight into the role of recombination events in shaping the genome of the SAR324 group based on a larger number of repeat regions observed, which has been overlooked thus far.</p> </li> <li> <p><a target="_blank" rel="noopener noreferrer" onclick="trackOutboundLink('https://www.pubmedcentral.nih.gov/articlerender.fcgi?tool=pmcentrez&artid=4782131','PMC'); return false;" href="https://www.pubmedcentral.nih.gov/articlerender.fcgi?tool=pmcentrez&artid=4782131"><span>Delta-proteobacterial SAR324 group in hydrothermal plumes on the South Mid-Atlantic Ridge</span></a></p> <p><a target="_blank" rel="noopener noreferrer" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?DB=pmc">PubMed Central</a></p> <p>Cao, Huiluo; Dong, Chunming; Bougouffa, Salim; Li, Jiangtao; Zhang, Weipeng; Shao, Zongze; Bajic, Vladimir B.; Qian, Pei-Yuan</p> <p>2016-01-01</p> <p>In the dark ocean, the SAR324 group of Delta-proteobacteria has been associated with a chemolithotrophic lifestyle. However, their electron transport chain for energy generation and information system has not yet been well characterized. In the present study, four SAR324 draft genomes were extracted from metagenomes sampled from hydrothermal plumes in the South Mid-Atlantic Ridge. We describe novel electron transport chain components in the SAR324 group, particularly the alternative complex III, which is involved in energy generation. Moreover, we propose that the C-type cytochrome, for example the C553, may play a novel role in electron transfer, adding to our knowledge regarding the energy generation process in the SAR324 cluster. The central carbon metabolism in the described SAR324 genomes exhibits several new features other than methanotrophy e.g. aromatic compound degradation. This suggests that methane oxidation may not be the main central carbon metabolism component in SAR324 cluster bacteria. The reductive acetyl-CoA pathway may potentially be essential in carbon fixation due to the absence of components from the Calvin-Benson cycle. Our study provides insight into the role of recombination events in shaping the genome of the SAR324 group based on a larger number of repeat regions observed, which has been overlooked thus far. PMID:26953077</p> </li> <li> <p><a target="_blank" rel="noopener noreferrer" onclick="trackOutboundLink('http://adsabs.harvard.edu/abs/2017PlST...19j5601P','NASAADS'); return false;" href="http://adsabs.harvard.edu/abs/2017PlST...19j5601P"><span>Repetitive cleaning of a stainless steel first mirror using radio frequency plasma</span></a></p> <p><a target="_blank" rel="noopener noreferrer" href="http://adsabs.harvard.edu/abstract_service.html">NASA Astrophysics Data System (ADS)</a></p> <p>Peng, Jiao; Yan, Rong; Ding, Rui; Chen, Junling; Zhu, Dahuan; Zhang, Zengming</p> <p>2017-10-01</p> <p>First mirrors (FMs) are crucial components of optical diagnostic systems in present-day tokamaks and future fusion reactors. Their lifetimes should be extremely limited due to their proximity to burning plasma, greatly influencing the safe operation of corresponding diagnostics. Repetitive cleaning is expected to provide a solution to the frequent replacement of contaminated FMs, thus prolonging their lifetimes. Three repetitive cleaning cycles using radio frequency plasma were applied to stainless steel (SS) FM samples, to evaluate the change of the mirrors’ optical properties and morphology during each cycle. Amorphous carbon films were deposited on mirror surfaces under identical conditions in three cycles. In three cycles with identical cleaning parameters, the total reflectivity was restored at up to 95%. Nevertheless, with successive cleaning cycles, the FM surfaces gradually appeared to roughen due to damage to the grain boundaries. Correspondingly, the diffuse reflectivity increased from a few percent to 20% and 27% after the second and third cycles. After optimizing the cleaning parameters of the second and third cycles, the roughness showed a significant decrease, and simultaneously the increase of diffuse reflectivity was remarkably improved.</p> </li> <li> <p><a target="_blank" rel="noopener noreferrer" onclick="trackOutboundLink('https://www.osti.gov/pages/biblio/1237303-reliability-emerging-bonded-interface-materials-large-area-attachments','SCIGOV-DOEP'); return false;" href="https://www.osti.gov/pages/biblio/1237303-reliability-emerging-bonded-interface-materials-large-area-attachments"><span>Reliability of emerging bonded interface materials for large-area attachments</span></a></p> <p><a target="_blank" rel="noopener noreferrer" href="http://www.osti.gov/pages">DOE PAGES</a></p> <p>Paret, Paul P.; DeVoto, Douglas J.; Narumanchi, Sreekant</p> <p>2015-12-30</p> <p>In this study, conventional thermal interface materials (TIMs), such as greases, gels, and phase change materials, pose bottlenecks to heat removal and have long caused reliability issues in automotive power electronics packages. Bonded interface materials (BIMs) with superior thermal performance have the potential to be a replacement to the conventional TIMs. However, due to coefficient of thermal expansion mismatches between different components in a package and resultant thermomechanical stresses, fractures or delamination could occur, causing serious reliability concerns. These defects manifest themselves in increased thermal resistance in the package. In this paper, the results of reliability evaluation of emerging BIMsmore » for large-area attachments in power electronics packaging are reported. Thermoplastic (polyamide) adhesive with embedded near-vertical-aligned carbon fibers, sintered silver, and conventional lead solder (Sn 63Pb 37) materials were bonded between 50.8 mm x 50.8 mm cross-sectional footprint silicon nitride substrates and copper base plate samples, and were subjected to accelerated thermal cycling until failure or 2500 cycles. Damage in the BIMs was monitored every 100 cycles by scanning acoustic microscopy. Thermoplastic with embedded carbon fibers performed the best with no defects, whereas sintered silver and lead solder failed at 2300 and 1400 thermal cycles, respectively. Besides thermal cycling, additional lead solder samples were subjected to thermal shock and thermal cycling with extended dwell periods. A finite element method (FEM)-based model was developed to simulate the behavior of lead solder under thermomechanical loading. Strain energy density per cycle results were calculated from the FEM simulations. A predictive lifetime model was formulated for lead solder by correlating strain energy density results extracted from modeling with cycles-to-failure obtained from experimental accelerated tests. A power-law-based approach was used to formulate the - redictive lifetime model.« less</p> </li> <li> <p><a target="_blank" rel="noopener noreferrer" onclick="trackOutboundLink('https://www.ncbi.nlm.nih.gov/pubmed/14503509','PUBMED'); return false;" href="https://www.ncbi.nlm.nih.gov/pubmed/14503509"><span>Mass exchange in an experimental new-generation life support system model based on biological regeneration of environment.</span></a></p> <p><a target="_blank" rel="noopener noreferrer" href="https://www.ncbi.nlm.nih.gov/entrez/query.fcgi?DB=pubmed">PubMed</a></p> <p>Tikhomirov, A A; Ushakova, S A; Manukovsky, N S; Lisovsky, G M; Kudenko, Yu A; Kovalev, V S; Gubanov, V G; Barkhatov, Yu V; Gribovskaya, I V; Zolotukhin, I G; Gros, J B; Lasseur, Ch</p> <p>2003-01-01</p> <p>An experimental model of a biological life support system was used to evaluate qualitative and quantitative parameters of the internal mass exchange. The photosynthesizing unit included the higher plant component (wheat and radish), and the heterotrophic unit consisted of a soil-like substrate, California worms, mushrooms and microbial microflora. The gas mass exchange involved evolution of oxygen by the photosynthesizing component and its uptake by the heterotroph component along with the formation and maintaining of the SLS structure, growth of mushrooms and California worms, human respiration, and some other processes. Human presence in the system in the form of "virtual human" that at regular intervals took part in the respirative gas exchange during the experiment. Experimental data demonstrated good oxygen/carbon dioxide balance, and the closure of the cycles of these gases was almost complete. The water cycle was nearly 100% closed. The main components in the water mass exchange were transpiration water and the watering solution with mineral elements. Human consumption of the edible plant biomass (grains and roots) was simulated by processing these products by a unique physicochemical method of oxidizing them to inorganic mineral compounds, which were then returned into the system and fully assimilated by the plants. The oxidation was achieved by "wet combustion" of organic biomass, using hydrogen peroxide following a special procedure, which does not require high temperature and pressure. Hydrogen peroxide is produced from the water inside the system. The closure of the cycle was estimated for individual elements and compounds. Stoichiometric proportions are given for the main components included in the experimental model of the system. Approaches to the mathematical modeling of the cycling processes are discussed, using the data of the experimental model. Nitrogen, as a representative of biogenic elements, shows an almost 100% closure of the cycle inside the system. The proposed experimental model of a biological system is discussed as a candidate for potential application in the investigations aimed at creating ecosystems with largely closed cycles of the internal mass exchange. The formation and maintenance of sustainable cycling of vitally important chemical elements and compounds in biological life support systems (BLSS) is an extremely pressing problem. To attain the stable functioning of biological life support systems (BLSS) and to maintain a high degree of closure of material cycles in than, it is essential to understand the character of mass exchange processes and stoichiometnc proportions of the initial and synthesized components of the system. c2003 COSPAR. Published by Elsevier Science Ltd. All rights reserved.</p> </li> <li> <p><a target="_blank" rel="noopener noreferrer" onclick="trackOutboundLink('http://adsabs.harvard.edu/abs/2017EGUGA..1916976S','NASAADS'); return false;" href="http://adsabs.harvard.edu/abs/2017EGUGA..1916976S"><span>Lateral variations of carbonate platform facies and cycles: The Dachstein Limestone (Late Triassic, Northern Calcareous Alps, Austria)</span></a></p> <p><a target="_blank" rel="noopener noreferrer" href="http://adsabs.harvard.edu/abstract_service.html">NASA Astrophysics Data System (ADS)</a></p> <p>Samankassou, Elias; Enos, Paul</p> <p>2017-04-01</p> <p>The driving mechanisms of cyclic patterns in shallow-water platform carbonates remain controversial. The focus of the present paper is to quantify lateral facies variations for a long stratigraphic record in an extensive, continuous, well-exposed cliff of the Dachstein platform that is composed, as many other Phanerozoic carbonate platforms, of peritidal deposits. We noted the lateral continuity of the beds to the degree permitted by the outcrop, generally a few tens or hundreds of meters; exceptionally up to 1.7 km. The study demonstrates the importance of quantification to evaluate origins of sedimentary cycles. The upper 885 m of the Triassic Dachstein platform limestone at Steinernes Meer, Saalfelden, Austria, includes 241 peritidal cycles overlain by 275 m of subtidal, non-cyclic and weakly cyclic limestone. Of 558 subtidal and intertidal beds measured, 121 (21.7%) disappear laterally. An additional 74 beds (13.3%) show significant (>10%) lateral variations in thickness. Mean thickness variation is 50%. Both lateral variations and discontinuities appear to lack a spatial vector. Disappearances toward the inferred platform interior (west), total 10.4% of the beds. East toward the inferred platform margin 11.3% of the beds disappear. Thickness changes occur in 6.6% of beds in each direction. The lack of lateral continuity of beds is consistent with a non-eustatic component to stratification. Erosion of intertidal intervals is the process that can be most readily documented. Erosion, transport, and non-uniform distribution of sediments, superposed on stratigraphic sequences driven by eustacy, are the likely processes which produced the complex, randomly recorded cycle patterns. Cycle duration may not be exclusively determined by Milankovitch processes, as suggested by the discrepancies in the cycle duration and interpretation among stratigraphers of the Dachstein, as well as other Phanerozoic carbonate platforms. Signals deduced from linearly measured sections likely represent composite inherent and extrabasinal factors; they should not be automatically interpreted as exclusive records of eustatic orbital forcing. Lateral discontinuities and thickness variations could also present problems in spectral analysis of thickness patterns, typically conducted in search of "Milankovich frequencies", as well as in construction of "Fischer plots," to analyze long-period oscillations in relative sea level. Any section subjected to cycle analysis should be examined for lateral changes, to the extent permitted by the exposures, in order to produce the most complete (composite) section possible.</p> </li> <li> <p><a target="_blank" rel="noopener noreferrer" onclick="trackOutboundLink('http://adsabs.harvard.edu/abs/2015AGUFMGC12B..12R','NASAADS'); return false;" href="http://adsabs.harvard.edu/abs/2015AGUFMGC12B..12R"><span>Advances on interdisciplinary approaches to urban carbon</span></a></p> <p><a target="_blank" rel="noopener noreferrer" href="http://adsabs.harvard.edu/abstract_service.html">NASA Astrophysics Data System (ADS)</a></p> <p>Romero-Lankao, P.</p> <p>2015-12-01</p> <p>North American urban areas are emerging as climate policy and technology innovators, urbanization process laboratories, fonts of carbon relevant experiments, hubs for grass-roots mobilization, and centers for civil-society experiments to curb carbon emissions and avoid widespread and irreversible climate impacts. Since SOCCR diverse lines of inquiry on urbanization, urban areas and the carbon cycle have advanced our understanding of some of the societal processes through which energy and land uses affect carbon. This presentation provides an overview of these diverse perspectives. It suggests the need for approaches that complement and combine the plethora of existing insights into interdisciplinary explorations of how different urbanization processes, and socio-ecological and technological components of urban areas affect the spatial and temporal patterns of carbon emissions, differentially over time and within and across cities. It also calls for a more holistic approach to examining the carbon implications of urbanization and urban areas as places, based not only on demographics or income, but also on such other interconnected features of urban development pathways as urban form, economic function, economic growth policies and climate policies.</p> </li> <li> <p><a target="_blank" rel="noopener noreferrer" onclick="trackOutboundLink('http://www.osti.gov/sciencecinema/biblio/1015163','SCIGOVIMAGE-SCICINEMA'); return false;" href="http://www.osti.gov/sciencecinema/biblio/1015163"><span>Energy Demand in China (Carbon Cycle 2.0)</span></a></p> <p><a target="_blank" rel="noopener noreferrer" href="http://www.osti.gov/sciencecinema/">ScienceCinema</a></p> <p>Price, Lynn</p> <p>2018-02-14</p> <p>Lynn Price, LBNL scientist, speaks at the Carbon Cycle 2.0 kick-off symposium Feb. 2, 2010. We emit more carbon into the atmosphere than natural processes are able to remove - an imbalance with negative consequences. Carbon Cycle 2.0 is a Berkeley Lab initiative to provide the science needed to restore this balance by integrating the Labs diverse research activities and delivering creative solutions toward a carbon-neutral energy future.</p> </li> <li> <p><a target="_blank" rel="noopener noreferrer" onclick="trackOutboundLink('http://www.osti.gov/sciencecinema/biblio/1015181','SCIGOVIMAGE-SCICINEMA'); return false;" href="http://www.osti.gov/sciencecinema/biblio/1015181"><span>Biofuels Science and Facilities (Carbon Cycle 2.0)</span></a></p> <p><a target="_blank" rel="noopener noreferrer" href="http://www.osti.gov/sciencecinema/">ScienceCinema</a></p> <p>Keasling, Jay D.</p> <p>2018-04-27</p> <p>Jay D. Keasling speaks at the Carbon Cycle 2.0 kick-off symposium Feb. 2, 2010. We emit more carbon into the atmosphere than natural processes are able to remove - an imbalance with negative consequences. Carbon Cycle 2.0 is a Berkeley Lab initiative to provide the science needed to restore this balance by integrating the Labs diverse research activities and delivering creative solutions toward a carbon-neutral energy future.</p> </li> <li> <p><a target="_blank" rel="noopener noreferrer" onclick="trackOutboundLink('http://www.osti.gov/sciencecinema/biblio/1015179','SCIGOVIMAGE-SCICINEMA'); return false;" href="http://www.osti.gov/sciencecinema/biblio/1015179"><span>Energy Storage: Breakthrough in Battery Technologies (Carbon Cycle 2.0)</span></a></p> <p><a target="_blank" rel="noopener noreferrer" href="http://www.osti.gov/sciencecinema/">ScienceCinema</a></p> <p>Balsara, Nitash</p> <p>2018-02-12</p> <p>Nitash Balsara speaks at the Carbon Cycle 2.0 kick-off symposium Feb. 2, 2010. We emit more carbon into the atmosphere than natural processes are able to remove - an imbalance with negative consequences. Carbon Cycle 2.0 is a Berkeley Lab initiative to provide the science needed to restore this balance by integrating the Labs diverse research activities and delivering creative solutions toward a carbon-neutral energy future.</p> </li> <li> <p><a target="_blank" rel="noopener noreferrer" onclick="trackOutboundLink('http://adsabs.harvard.edu/abs/2014JPS...270..608B','NASAADS'); return false;" href="http://adsabs.harvard.edu/abs/2014JPS...270..608B"><span>Various supercritical carbon dioxide cycle layouts study for molten carbonate fuel cell application</span></a></p> <p><a target="_blank" rel="noopener noreferrer" href="http://adsabs.harvard.edu/abstract_service.html">NASA Astrophysics Data System (ADS)</a></p> <p>Bae, Seong Jun; Ahn, Yoonhan; Lee, Jekyoung; Lee, Jeong Ik</p> <p>2014-12-01</p> <p>Various supercritical carbon dioxide (S-CO2) cycles for a power conversion system of a Molten Carbonate Fuel Cell (MCFC) hybrid system are studied in this paper. Re-Compressing Brayton (RCB) cycle, Simple Recuperated Brayton (SRB) cycle and Simple Recuperated Transcritical (SRT) cycle layouts were selected as candidates for this study. In addition, a novel concept of S-CO2 cycle which combines Brayton cycle and Rankine cycle is proposed and intensively studied with other S-CO2 layouts. A parametric study is performed to optimize the total system to be compact and to achieve wider operating range. Performances of each S-CO2 cycle are compared in terms of the thermal efficiency, net electricity of the MCFC hybrid system and approximate total volumes of each S-CO2 cycle. As a result, performance and total physical size of S-CO2 cycle can be better understood for MCFC S-CO2 hybrid system and especially, newly suggested S-CO2 cycle shows some success.</p> </li> <li> <p><a target="_blank" rel="noopener noreferrer" onclick="trackOutboundLink('http://adsabs.harvard.edu/abs/2014EGUGA..16.3179K','NASAADS'); return false;" href="http://adsabs.harvard.edu/abs/2014EGUGA..16.3179K"><span>Contribution of aboveground plant respiration to carbon cycling in a Bornean tropical rainforet</span></a></p> <p><a target="_blank" rel="noopener noreferrer" href="http://adsabs.harvard.edu/abstract_service.html">NASA Astrophysics Data System (ADS)</a></p> <p>Katayama, Ayumi; Tanaka, Kenzo; Ichie, Tomoaki; Kume, Tomonori; Matsumoto, Kazuho; Ohashi, Mizue; Kumagai, Tomo'omi</p> <p>2014-05-01</p> <p>Bornean tropical rainforests have a different characteristic from Amazonian tropical rainforests, that is, larger aboveground biomass caused by higher stand density of large trees. Larger biomass may cause different carbon cycling and allocation pattern. However, there are fewer studies on carbon allocation and each component in Bornean tropical rainforests, especially for aboveground plant respiration, compared to Amazonian forests. In this study, we measured woody tissue respiration and leaf respiration, and estimated those in ecosystem scale in a Bornean tropical rainforest. Then, we examined carbon allocation using the data of soil respiration and aboveground net primary production obtained from our previous studies. Woody tissue respiration rate was positively correlated with diameter at breast height (dbh) and stem growth rate. Using the relationships and biomass data, we estimated woody tissue respiration in ecosystem scale though methods of scaling resulted in different estimates values (4.52 - 9.33 MgC ha-1 yr-1). Woody tissue respiration based on surface area (8.88 MgC ha-1 yr-1) was larger than those in Amazon because of large aboveground biomass (563.0 Mg ha-1). Leaf respiration rate was positively correlated with height. Using the relationship and leaf area density data at each 5-m height, leaf respiration in ecosystem scale was estimated (9.46 MgC ha-1 yr-1), which was similar to those in Amazon because of comparable LAI (5.8 m2 m-2). Gross primary production estimated from biometric measurements (44.81 MgC ha-1 yr-1) was much higher than those in Amazon, and more carbon was allocated to woody tissue respiration and total belowground carbon flux. Large tree with dbh > 60cm accounted for about half of aboveground biomass and aboveground biomass increment. Soil respiration was also related to position of large trees, resulting in high soil respiration rate in this study site. Photosynthesis ability of top canopy for large trees was high and leaves for the large trees accounted for 30% of total, which can lead high GPP. These results suggest that large trees play considerable role in carbon cycling and make a distinctive carbon allocation in the Bornean tropical rainforest.</p> </li> <li> <p><a target="_blank" rel="noopener noreferrer" onclick="trackOutboundLink('http://adsabs.harvard.edu/abs/2016ThEng..63..404A','NASAADS'); return false;" href="http://adsabs.harvard.edu/abs/2016ThEng..63..404A"><span>Prospects of development of highly mineralized high-temperature resources of the Tarumovskoye geothermal field</span></a></p> <p><a target="_blank" rel="noopener noreferrer" href="http://adsabs.harvard.edu/abstract_service.html">NASA Astrophysics Data System (ADS)</a></p> <p>Alkhasov, A. B.; Alkhasova, D. A.; Ramazanov, A. Sh.; Kasparova, M. A.</p> <p>2016-06-01</p> <p>The promising nature of integrated processing of high-temperature geothermal brines of the Tarumovskoye geothermal field is shown. Thermal energy of a geothermal brine can be converted to the electric power at a binary geothermal power plant (GPP) based on low-boiling working substance. The thermodynamic Rankine cycles are considered which are implemented in the GPP secondary loop at different evaporation temperatures of the working substance―isobutane. Among them, the most efficient cycle from the standpoint of attaining a maximum power is the supercritical one which is close to the so-called triangular cycle with an evaporation pressure of p e = 5.0 MPa. The used low-temperature brine is supplied from the GPP to a chemical plant, where main chemical components (lithium carbonate, burnt magnesia, calcium carbonate, and sodium chloride) are extracted from it according to the developed technology of comprehensive utilization of geothermal brines of chloride-sodium type. The waste water is delivered to the geotechnological complex and other consumers. For producing valuable inorganic materials, the electric power generated at the GPP is used. Owing to this, the total self-sufficiency of production and independence from external conditions is achieved. The advantages of the proposed geotechnological complex are the full utilization of the heat potential and the extraction of main chemical components of multiparameter geothermal resources. In this case, there is no need for reverse pumping, which eliminates the significant capital costs for building injection wells and a pumping station and the operating costs for their service. A characteristic of the modern state of the field and estimated figures of the integrated processing of high-temperature brines of well no. 6 are given, from which it follows that the proposed technology has a high efficiency. The comprehensive development of the field resources will make it possible to improve the economic structure of the region and fully meet the needs of Russia in lithium carbonate and sodium chloride.</p> </li> <li> <p><a target="_blank" rel="noopener noreferrer" onclick="trackOutboundLink('https://www.gpo.gov/fdsys/pkg/CFR-2012-title40-vol12/pdf/CFR-2012-title40-vol12-part63-subpartOOO-app3.pdf','CFR2012'); return false;" href="https://www.gpo.gov/fdsys/pkg/CFR-2012-title40-vol12/pdf/CFR-2012-title40-vol12-part63-subpartOOO-app3.pdf"><span>40 CFR Table 3 to Subpart Ooo of... - Batch Process Vent Monitoring Requirements</span></a></p> <p><a target="_blank" rel="noopener noreferrer" href="http://www.gpo.gov/fdsys/browse/collectionCfr.action?selectedYearFrom=2012&page.go=Go">Code of Federal Regulations, 2012 CFR</a></p> <p></p> <p>2012-07-01</p> <p>... specified in § 63.1416(d). a Carbon adsorber a Total regeneration steam flow or nitrogen flow, or pressure (gauge or absolute) during carbon bed regeneration cycle(s), and Record the total regeneration steam flow or nitrogen flow, or pressure for each carbon bed regeneration cycle. Temperature of the carbon bed...</p> </li> </ol> <div class="pull-right"> <ul class="pagination"> <li><a href="#" onclick='return showDiv("page_1");'>«</a></li> <li><a href="#" onclick='return showDiv("page_16");'>16</a></li> <li><a href="#" onclick='return showDiv("page_17");'>17</a></li> <li class="active"><span>18</span></li> <li><a href="#" onclick='return showDiv("page_19");'>19</a></li> <li><a href="#" onclick='return showDiv("page_20");'>20</a></li> <li><a href="#" onclick='return showDiv("page_25");'>»</a></li> </ul> </div> </div><!-- col-sm-12 --> </div><!-- row --> </div><!-- page_18 --> <div id="page_19" class="hiddenDiv"> <div class="row"> <div class="col-sm-12"> <div class="pull-right"> <ul class="pagination"> <li><a href="#" onclick='return showDiv("page_1");'>«</a></li> <li><a href="#" onclick='return showDiv("page_17");'>17</a></li> <li><a href="#" onclick='return showDiv("page_18");'>18</a></li> <li class="active"><span>19</span></li> <li><a href="#" onclick='return showDiv("page_20");'>20</a></li> <li><a href="#" onclick='return showDiv("page_21");'>21</a></li> <li><a href="#" onclick='return showDiv("page_25");'>»</a></li> </ul> </div> </div> </div> <div class="row"> <div class="col-sm-12"> <ol class="result-class" start="361"> <li> <p><a target="_blank" rel="noopener noreferrer" onclick="trackOutboundLink('https://www.gpo.gov/fdsys/pkg/CFR-2010-title40-vol11/pdf/CFR-2010-title40-vol11-part63-subpartOOO-app3.pdf','CFR'); return false;" href="https://www.gpo.gov/fdsys/pkg/CFR-2010-title40-vol11/pdf/CFR-2010-title40-vol11-part63-subpartOOO-app3.pdf"><span>40 CFR Table 3 to Subpart Ooo of... - Batch Process Vent Monitoring Requirements</span></a></p> <p><a target="_blank" rel="noopener noreferrer" href="http://www.gpo.gov/fdsys/browse/collectionCfr.action?selectedYearFrom=2010&page.go=Go">Code of Federal Regulations, 2010 CFR</a></p> <p></p> <p>2010-07-01</p> <p>... specified in § 63.1416(d). a Carbon adsorber a Total regeneration steam flow or nitrogen flow, or pressure (gauge or absolute) during carbon bed regeneration cycle(s), and Record the total regeneration steam flow or nitrogen flow, or pressure for each carbon bed regeneration cycle. Temperature of the carbon bed...</p> </li> <li> <p><a target="_blank" rel="noopener noreferrer" onclick="trackOutboundLink('https://www.gpo.gov/fdsys/pkg/CFR-2011-title40-vol11/pdf/CFR-2011-title40-vol11-part63-subpartOOO-app3.pdf','CFR2011'); return false;" href="https://www.gpo.gov/fdsys/pkg/CFR-2011-title40-vol11/pdf/CFR-2011-title40-vol11-part63-subpartOOO-app3.pdf"><span>40 CFR Table 3 to Subpart Ooo of... - Batch Process Vent Monitoring Requirements</span></a></p> <p><a target="_blank" rel="noopener noreferrer" href="http://www.gpo.gov/fdsys/browse/collectionCfr.action?selectedYearFrom=2011&page.go=Go">Code of Federal Regulations, 2011 CFR</a></p> <p></p> <p>2011-07-01</p> <p>... specified in § 63.1416(d). a Carbon adsorber a Total regeneration steam flow or nitrogen flow, or pressure (gauge or absolute) during carbon bed regeneration cycle(s), and Record the total regeneration steam flow or nitrogen flow, or pressure for each carbon bed regeneration cycle. Temperature of the carbon bed...</p> </li> <li> <p><a target="_blank" rel="noopener noreferrer" onclick="trackOutboundLink('http://hdl.handle.net/2060/20040082117','NASA-TRS'); return false;" href="http://hdl.handle.net/2060/20040082117"><span>Observing Human-induced Linkages between Urbanization and Earth's Climate System</span></a></p> <p><a target="_blank" rel="noopener noreferrer" href="http://ntrs.nasa.gov/search.jsp">NASA Technical Reports Server (NTRS)</a></p> <p>Shepherd, J. Marshall; Jin, Menglin</p> <p>2004-01-01</p> <p>Urbanization is one of the extreme cases of land use change. Most of world s population has moved to urban areas. Although currently only 1.2% of the land is considered urban, the spatial coverage and density of cities are expected to rapidly increase in the near future. It is estimated that by the year 2025, 60% of the world s population will live in cities. Human activity in urban environments also alters atmospheric composition; impacts components of the water cycle; and modifies the carbon cycle and ecosystems. However, our understanding of urbanization on the total Earth-climate system is incomplete. Better understanding of how the Earth s atmosphere-ocean-land-biosphere components interact as a coupled system and the influence of the urban environment on this climate system is critical. The goal of the 2003 AGU Union session Human-induced climate variations on urban areas: From observations to modeling was to bring together scientists from interdisciplinary backgrounds to discuss the data, scientific approaches and recent results on observing and modeling components of the urban environment with the intent of sampling our current stand and discussing future direction on this topic. Herein, a summary and discussion of the observations component of the session are presented.</p> </li> <li> <p><a target="_blank" rel="noopener noreferrer" onclick="trackOutboundLink('http://adsabs.harvard.edu/abs/2013EOSTr..94..184M','NASAADS'); return false;" href="http://adsabs.harvard.edu/abs/2013EOSTr..94..184M"><span>Progress and Future Directions in North American Carbon Cycle Science</span></a></p> <p><a target="_blank" rel="noopener noreferrer" href="http://adsabs.harvard.edu/abstract_service.html">NASA Astrophysics Data System (ADS)</a></p> <p>Michalak, Anna; Huntzinger, Deborah; Shrestha, Gyami</p> <p>2013-05-01</p> <p>The North American Carbon Program (NACP) convened its fourth biennial "All Investigators" meeting (AIM4, http://www.nacarbon.org/meeting_2013) to review progress in understanding the dynamics of the carbon cycle of North America and adjacent oceans and to chart a course for a more integrative and holistic approach to future research. The meeting was structured around the six decadal goals outlined in the new "A U.S. Carbon Cycle Science Plan" (Michalak et al., University Corporation for Atmospheric Research, 2011, available at http://www.carboncyclescience.gov) and focused on (1) diagnosis of the atmospheric carbon cycle, (2) drivers of anthropogenic emissions, (3) vulnerability of carbon stocks to change, (4) ecosystem impacts of change, (5) carbon management, and (6) decision support.</p> </li> <li> <p><a target="_blank" rel="noopener noreferrer" onclick="trackOutboundLink('http://adsabs.harvard.edu/abs/2014AGUFM.B23K0134G','NASAADS'); return false;" href="http://adsabs.harvard.edu/abs/2014AGUFM.B23K0134G"><span>Molecular profiling of permafrost soil organic carbon composition and degradation</span></a></p> <p><a target="_blank" rel="noopener noreferrer" href="http://adsabs.harvard.edu/abstract_service.html">NASA Astrophysics Data System (ADS)</a></p> <p>Gu, B.; Mann, B.</p> <p>2014-12-01</p> <p>Microbial degradation of soil organic matter (SOM) is a key process for terrestrial carbon (C) cycling, though the dynamics of these transformations remain unclear at the molecular level. This study reports the application of ultrahigh resolution Fourier transform ion cyclotron resonance mass spectrometry (FTICR-MS) to profile molecular components of Arctic SOM collected from the surface water and the mineral horizon of a low-centered polygon soil at Barrow Environmental Observatory (BEO), Barrow, Alaska. Soil samples were subjected to anaerobic warming experiments for a period of 40 days, and the SOM was extracted before and after the incubation to determine the components of organic C that were degraded over the course of the study. A CHO index based on molecular composition data was utilized to codify SOM components according to their observed degradation potential. Carbohydrate- and lignin-like compounds in the water-soluble fraction (WSF) demonstrated a high degradation potential, while structures with similar stoichiometries in the base-soluble fraction (BSF) were not readily degraded. The WSF of SOM also shifted to a wider range of measured molecular masses including an increased prevalence of larger compounds, while the size distribution of compounds in the BSF changed little over the same period. Additionally, the molecular profiling data indicated an apparently ordered incorporation of organic nitrogen in the BSF immobilized as primary and secondary amines, possibly as components of N-heterocycles, which may provide insight into nitrogen immobilization or mobilization processes in SOM. Our study represents an important step forward for studying Arctic SOM with improved understanding of the molecular properties of soil organic C and the ability to represent SOM in climate models that will predict the impact of climate change on soil C and nutrient cycling.</p> </li> <li> <p><a target="_blank" rel="noopener noreferrer" onclick="trackOutboundLink('https://www.ncbi.nlm.nih.gov/pubmed/29253908','PUBMED'); return false;" href="https://www.ncbi.nlm.nih.gov/pubmed/29253908"><span>Cytotoxic Deoxypodophyllotoxin Can Be Extracted in High Purity from Anthriscus sylvestris Roots by Supercritical Carbon Dioxide.</span></a></p> <p><a target="_blank" rel="noopener noreferrer" href="https://www.ncbi.nlm.nih.gov/entrez/query.fcgi?DB=pubmed">PubMed</a></p> <p>Seegers, Christel L C; Tepper, Pieter G; Setroikromo, Rita; Quax, Wim J</p> <p>2018-05-01</p> <p>Deoxypodophyllotoxin is present in the roots of Anthriscus sylvestris . This compound is cytotoxic on its own, but it can also be converted into podophyllotoxin, which is in high demand as a precursor for the important anticancer drugs etoposide and teniposide. In this study, deoxypodophyllotoxin is extracted from A. sylvestris roots by supercritical carbon dioxide extraction. The process is simple and scalable. The supercritical carbon dioxide method extracts 75 - 80% of the total deoxypodophyllotoxin content, which is comparable to a single extraction by traditional Soxhlet. However, less polar components are extracted. The activity of the supercritical carbon dioxide extract containing deoxypodophyllotoxin was assessed by demonstrating that the extract arrests A549 and HeLa cells in the G 2 /M phase of the cell cycle. We conclude that biologically active deoxypodophyllotoxin can be extracted from A. sylvestris by supercritical carbon dioxide extraction. The method is solvent free and more sustainable compared to traditional methods. Georg Thieme Verlag KG Stuttgart · New York.</p> </li> <li> <p><a target="_blank" rel="noopener noreferrer" onclick="trackOutboundLink('https://www.pubmedcentral.nih.gov/articlerender.fcgi?tool=pmcentrez&artid=5383274','PMC'); return false;" href="https://www.pubmedcentral.nih.gov/articlerender.fcgi?tool=pmcentrez&artid=5383274"><span>Decay and nutrient dynamics of coarse woody debris in the Qinling Mountains, China</span></a></p> <p><a target="_blank" rel="noopener noreferrer" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?DB=pmc">PubMed Central</a></p> <p>Yuan, Jie; Hou, Lin; Wei, Xin; Shang, Zhengchun; Cheng, Fei; Zhang, Shuoxin</p> <p>2017-01-01</p> <p>As an ecological unit, coarse woody debris (CWD) plays an essential role in productivity, nutrient cycling, carbon sequestration, community regeneration and biodiversity. However, thus far, the information on quantification the decomposition and nutrient content of CWD in forest ecosystems remains considerably limited. In this study, we conducted a long-term (1996–2013) study on decay and nutrient dynamics of CWD for evaluating accurately the ecological value of CWD on the Huoditang Experimental Forest Farm in the Qinling Mountains, China. The results demonstrated that there was a strong correlation between forest biomass and CWD mass. The single exponential decay model well fit the CWD density loss at this site, and as the CWD decomposed, the CWD density decreased significantly. Annual temperature and precipitation were all significantly correlated with the annual mass decay rate. The K contents and the C/N ratio of the CWD decreased as the CWD decayed, but the C, N, P, Ca and Mg contents increased. We observed a significant CWD decay effect on the soil C, N and Mg contents, especially the soil C content. The soil N, P, K, Ca and Mg contents exhibited large fluctuations, but the variation had no obvious regularity and changed with different decay times. The results showed that CWD was a critical component of nutrient cycling in forest ecosystems. Further research is needed to determine the effect of diameter, plant tissue components, secondary wood compounds, and decomposer organisms on the CWD decay rates in the Qinling Mountains, which will be beneficial to clarifying the role of CWD in carbon cycles of forest ecosystems. PMID:28384317</p> </li> <li> <p><a target="_blank" rel="noopener noreferrer" onclick="trackOutboundLink('http://adsabs.harvard.edu/abs/2016IJAEO..52..149C','NASAADS'); return false;" href="http://adsabs.harvard.edu/abs/2016IJAEO..52..149C"><span>Estimating dissolved organic carbon concentration in turbid coastal waters using optical remote sensing observations</span></a></p> <p><a target="_blank" rel="noopener noreferrer" href="http://adsabs.harvard.edu/abstract_service.html">NASA Astrophysics Data System (ADS)</a></p> <p>Cherukuru, Nagur; Ford, Phillip W.; Matear, Richard J.; Oubelkheir, Kadija; Clementson, Lesley A.; Suber, Ken; Steven, Andrew D. L.</p> <p>2016-10-01</p> <p>Dissolved Organic Carbon (DOC) is an important component in the global carbon cycle. It also plays an important role in influencing the coastal ocean biogeochemical (BGC) cycles and light environment. Studies focussing on DOC dynamics in coastal waters are data constrained due to the high costs associated with in situ water sampling campaigns. Satellite optical remote sensing has the potential to provide continuous, cost-effective DOC estimates. In this study we used a bio-optics dataset collected in turbid coastal waters of Moreton Bay (MB), Australia, during 2011 to develop a remote sensing algorithm to estimate DOC. This dataset includes data from flood and non-flood conditions. In MB, DOC concentration varied over a wide range (20-520 μM C) and had a good correlation (R2 = 0.78) with absorption due to coloured dissolved organic matter (CDOM) and remote sensing reflectance. Using this data set we developed an empirical algorithm to derive DOC concentrations from the ratio of Rrs(412)/Rrs(488) and tested it with independent datasets. In this study, we demonstrate the ability to estimate DOC using remotely sensed optical observations in turbid coastal waters.</p> </li> <li> <p><a target="_blank" rel="noopener noreferrer" onclick="trackOutboundLink('https://pubs.er.usgs.gov/publication/70182178','USGSPUBS'); return false;" href="https://pubs.er.usgs.gov/publication/70182178"><span>Source limitation of carbon gas emissions in high-elevation mountain streams and lakes</span></a></p> <p><a target="_blank" rel="noopener noreferrer" href="http://pubs.er.usgs.gov/pubs/index.jsp?view=adv">USGS Publications Warehouse</a></p> <p>Crawford, John T.; Dornblaser, Mark M.; Stanley, Emily H.; Clow, David W.; Striegl, Robert G.</p> <p>2015-01-01</p> <p>Inland waters are an important component of the global carbon cycle through transport, storage, and direct emissions of CO2 and CH4 to the atmosphere. Despite predictions of high physical gas exchange rates due to turbulent flows and ubiquitous supersaturation of CO2—and perhaps also CH4—patterns of gas emissions are essentially undocumented for high mountain ecosystems. Much like other headwater networks around the globe, we found that high-elevation streams in Rocky Mountain National Park, USA, were supersaturated with CO2 during the growing season and were net sources to the atmosphere. CO2concentrations in lakes, on the other hand, tended to be less than atmospheric equilibrium during the open water season. CO2 and CH4 emissions from the aquatic conduit were relatively small compared to many parts of the globe. Irrespective of the physical template for high gas exchange (high k), we found evidence of CO2 source limitation to mountain streams during the growing season, which limits overall CO2emissions. Our results suggest a reduced importance of aquatic ecosystems for carbon cycling in high-elevation landscapes having limited soil development and high CO2 consumption via mineral weathering.</p> </li> <li> <p><a target="_blank" rel="noopener noreferrer" onclick="trackOutboundLink('https://www.ncbi.nlm.nih.gov/pubmed/28931949','PUBMED'); return false;" href="https://www.ncbi.nlm.nih.gov/pubmed/28931949"><span>Hydrothermal activity, functional diversity and chemoautotrophy are major drivers of seafloor carbon cycling.</span></a></p> <p><a target="_blank" rel="noopener noreferrer" href="https://www.ncbi.nlm.nih.gov/entrez/query.fcgi?DB=pubmed">PubMed</a></p> <p>Bell, James B; Woulds, Clare; Oevelen, Dick van</p> <p>2017-09-20</p> <p>Hydrothermal vents are highly dynamic ecosystems and are unusually energy rich in the deep-sea. In situ hydrothermal-based productivity combined with sinking photosynthetic organic matter in a soft-sediment setting creates geochemically diverse environments, which remain poorly studied. Here, we use comprehensive set of new and existing field observations to develop a quantitative ecosystem model of a deep-sea chemosynthetic ecosystem from the most southerly hydrothermal vent system known. We find evidence of chemosynthetic production supplementing the metazoan food web both at vent sites and elsewhere in the Bransfield Strait. Endosymbiont-bearing fauna were very important in supporting the transfer of chemosynthetic carbon into the food web, particularly to higher trophic levels. Chemosynthetic production occurred at all sites to varying degrees but was generally only a small component of the total organic matter inputs to the food web, even in the most hydrothermally active areas, owing in part to a low and patchy density of vent-endemic fauna. Differences between relative abundance of faunal functional groups, resulting from environmental variability, were clear drivers of differences in biogeochemical cycling and resulted in substantially different carbon processing patterns between habitats.</p> </li> <li> <p><a target="_blank" rel="noopener noreferrer" onclick="trackOutboundLink('https://www.pubmedcentral.nih.gov/articlerender.fcgi?tool=pmcentrez&artid=4438322','PMC'); return false;" href="https://www.pubmedcentral.nih.gov/articlerender.fcgi?tool=pmcentrez&artid=4438322"><span>A multitrophic model to quantify the effects of marine viruses on microbial food webs and ecosystem processes</span></a></p> <p><a target="_blank" rel="noopener noreferrer" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?DB=pmc">PubMed Central</a></p> <p>Weitz, Joshua S; Stock, Charles A; Wilhelm, Steven W; Bourouiba, Lydia; Coleman, Maureen L; Buchan, Alison; Follows, Michael J; Fuhrman, Jed A; Jover, Luis F; Lennon, Jay T; Middelboe, Mathias; Sonderegger, Derek L; Suttle, Curtis A; Taylor, Bradford P; Frede Thingstad, T; Wilson, William H; Eric Wommack, K</p> <p>2015-01-01</p> <p>Viral lysis of microbial hosts releases organic matter that can then be assimilated by nontargeted microorganisms. Quantitative estimates of virus-mediated recycling of carbon in marine waters, first established in the late 1990s, were originally extrapolated from marine host and virus densities, host carbon content and inferred viral lysis rates. Yet, these estimates did not explicitly incorporate the cascade of complex feedbacks associated with virus-mediated lysis. To evaluate the role of viruses in shaping community structure and ecosystem functioning, we extend dynamic multitrophic ecosystem models to include a virus component, specifically parameterized for processes taking place in the ocean euphotic zone. Crucially, we are able to solve this model analytically, facilitating evaluation of model behavior under many alternative parameterizations. Analyses reveal that the addition of a virus component promotes the emergence of complex communities. In addition, biomass partitioning of the emergent multitrophic community is consistent with well-established empirical norms in the surface oceans. At steady state, ecosystem fluxes can be probed to characterize the effects that viruses have when compared with putative marine surface ecosystems without viruses. The model suggests that ecosystems with viruses will have (1) increased organic matter recycling, (2) reduced transfer to higher trophic levels and (3) increased net primary productivity. These model findings support hypotheses that viruses can have significant stimulatory effects across whole-ecosystem scales. We suggest that existing efforts to predict carbon and nutrient cycling without considering virus effects are likely to miss essential features of marine food webs that regulate global biogeochemical cycles. PMID:25635642</p> </li> <li> <p><a target="_blank" rel="noopener noreferrer" onclick="trackOutboundLink('https://www.ncbi.nlm.nih.gov/pubmed/25635642','PUBMED'); return false;" href="https://www.ncbi.nlm.nih.gov/pubmed/25635642"><span>A multitrophic model to quantify the effects of marine viruses on microbial food webs and ecosystem processes.</span></a></p> <p><a target="_blank" rel="noopener noreferrer" href="https://www.ncbi.nlm.nih.gov/entrez/query.fcgi?DB=pubmed">PubMed</a></p> <p>Weitz, Joshua S; Stock, Charles A; Wilhelm, Steven W; Bourouiba, Lydia; Coleman, Maureen L; Buchan, Alison; Follows, Michael J; Fuhrman, Jed A; Jover, Luis F; Lennon, Jay T; Middelboe, Mathias; Sonderegger, Derek L; Suttle, Curtis A; Taylor, Bradford P; Frede Thingstad, T; Wilson, William H; Eric Wommack, K</p> <p>2015-06-01</p> <p>Viral lysis of microbial hosts releases organic matter that can then be assimilated by nontargeted microorganisms. Quantitative estimates of virus-mediated recycling of carbon in marine waters, first established in the late 1990s, were originally extrapolated from marine host and virus densities, host carbon content and inferred viral lysis rates. Yet, these estimates did not explicitly incorporate the cascade of complex feedbacks associated with virus-mediated lysis. To evaluate the role of viruses in shaping community structure and ecosystem functioning, we extend dynamic multitrophic ecosystem models to include a virus component, specifically parameterized for processes taking place in the ocean euphotic zone. Crucially, we are able to solve this model analytically, facilitating evaluation of model behavior under many alternative parameterizations. Analyses reveal that the addition of a virus component promotes the emergence of complex communities. In addition, biomass partitioning of the emergent multitrophic community is consistent with well-established empirical norms in the surface oceans. At steady state, ecosystem fluxes can be probed to characterize the effects that viruses have when compared with putative marine surface ecosystems without viruses. The model suggests that ecosystems with viruses will have (1) increased organic matter recycling, (2) reduced transfer to higher trophic levels and (3) increased net primary productivity. These model findings support hypotheses that viruses can have significant stimulatory effects across whole-ecosystem scales. We suggest that existing efforts to predict carbon and nutrient cycling without considering virus effects are likely to miss essential features of marine food webs that regulate global biogeochemical cycles.</p> </li> <li> <p><a target="_blank" rel="noopener noreferrer" onclick="trackOutboundLink('http://www.osti.gov/sciencecinema/biblio/987893','SCIGOVIMAGE-SCICINEMA'); return false;" href="http://www.osti.gov/sciencecinema/biblio/987893"><span>Carbon Cycle 2.0: Ashok Gadgil: global impact</span></a></p> <p><a target="_blank" rel="noopener noreferrer" href="http://www.osti.gov/sciencecinema/">ScienceCinema</a></p> <p>Ashok Gadgi</p> <p>2017-12-09</p> <p>Ashok Gadgil speaks at the Carbon Cycle 2.0 kick-off symposium Feb. 2, 2010. We emit more carbon into the atmosphere than natural processes are able to remove - an imbalance with negative consequences. Carbon Cycle 2.0 is a Berkeley Lab initiative to provide the science needed to restore this balance by integrating the Labs diverse research activities and delivering creative solutions toward a carbon-neutral energy future. http://carboncycle2.lbl.gov/</p> </li> <li> <p><a target="_blank" rel="noopener noreferrer" onclick="trackOutboundLink('http://www.osti.gov/sciencecinema/biblio/1015177','SCIGOVIMAGE-SCICINEMA'); return false;" href="http://www.osti.gov/sciencecinema/biblio/1015177"><span>Low Cost Solar Energy Conversion (Carbon Cycle 2.0)</span></a></p> <p><a target="_blank" rel="noopener noreferrer" href="http://www.osti.gov/sciencecinema/">ScienceCinema</a></p> <p>Ramesh, Ramamoorthy</p> <p>2018-04-27</p> <p>Ramamoorthy Ramesh from LBNL's Materials Science Division speaks at the Carbon Cycle 2.0 kick-off symposium Feb. 2, 2010. We emit more carbon into the atmosphere than natural processes are able to remove - an imbalance with negative consequences. Carbon Cycle 2.0 is a Berkeley Lab initiative to provide the science needed to restore this balance by integrating the Labs diverse research activities and delivering creative solutions toward a carbon-neutral energy future.</p> </li> <li> <p><a target="_blank" rel="noopener noreferrer" onclick="trackOutboundLink('http://adsabs.harvard.edu/abs/2016AGUFMPP53E..02B','NASAADS'); return false;" href="http://adsabs.harvard.edu/abs/2016AGUFMPP53E..02B"><span>A Model for the Decrease in Amplitude of Carbon Isotope Excursions Throughout the Phanerozoic</span></a></p> <p><a target="_blank" rel="noopener noreferrer" href="http://adsabs.harvard.edu/abstract_service.html">NASA Astrophysics Data System (ADS)</a></p> <p>Bachan, A.; Lau, K. V.; Saltzman, M.; Thomas, E.; Kump, L. R.; Payne, J.</p> <p>2016-12-01</p> <p>The geological cycling of carbon ties the ocean-atmosphere carbon pool to Earth's biosphere and sedimentary reservoirs. Perturbations to this coupled system are recorded in the carbon-isotopic (δ13C) composition of marine carbonates. Large amplitude δ13C variations with durations of 0.5 - 10 m.y. are typically treated as individual events and interpreted accordingly. However, a recent compilation of Phanerozoic data reveals a decline in the variance of the δ13C record over time, suggesting a common underlying control. Here we propose that the redox structure of the continental shelves was a key determinant of the sensitivity of the geologic carbon cycle: when oxygen minimum zones (OMZs) were large, shallow, and prone to expansion, recurrent physical forcings (such as sea level and tectonics) would have had the capacity to drive large changes in the areal extent of OMZs, resulting in a strong leverage on δ13C values. Using a simple model of the geologic carbon cycle, we demonstrate that interactions between the carbon and phosphate cycles can result in amplification of recurrent forcings with periods in the 0.5 - 10 m.y. range. Thus, rather than requiring that physical forcings have their largest amplitude of variation on those time scales, enhanced sensitivity of the carbon cycle can account for the characteristic duration of δ13C excursions. Biologically mediated aspects of geologic carbon cycling, including the depth of bioturbation and evolution of pelagic calcifiers, likely drove a decline in the depth and extent of ocean anoxia over the Phanerozoic resulting in the stabilization of the geologic carbon cycle.</p> </li> <li> <p><a target="_blank" rel="noopener noreferrer" onclick="trackOutboundLink('https://www.ncbi.nlm.nih.gov/pubmed/17008211','PUBMED'); return false;" href="https://www.ncbi.nlm.nih.gov/pubmed/17008211"><span>The carbon cycle on early Earth--and on Mars?</span></a></p> <p><a target="_blank" rel="noopener noreferrer" href="https://www.ncbi.nlm.nih.gov/entrez/query.fcgi?DB=pubmed">PubMed</a></p> <p>Grady, Monica M; Wright, Ian</p> <p>2006-10-29</p> <p>One of the goals of the present Martian exploration is to search for evidence of extinct (or even extant) life. This could be redefined as a search for carbon. The carbon cycle (or, more properly, cycles) on Earth is a complex interaction among three reservoirs: the atmosphere; the hydrosphere; and the lithosphere. Superimposed on this is the biosphere, and its presence influences the fixing and release of carbon in these reservoirs over different time-scales. The overall carbon balance is kept at equilibrium on the surface by a combination of tectonic processes (which bury carbon), volcanism (which releases it) and biology (which mediates it). In contrast to Earth, Mars presently has no active tectonic system; neither does it possess a significant biosphere. However, these observations might not necessarily have held in the past. By looking at how Earth's carbon cycles have changed with time, as both the Earth's tectonic structure and a more sophisticated biology have evolved, and also by constructing a carbon cycle for Mars based on the carbon chemistry of Martian meteorites, we investigate whether or not there is evidence for a Martian biosphere.</p> </li> <li> <p><a target="_blank" rel="noopener noreferrer" onclick="trackOutboundLink('https://www.pubmedcentral.nih.gov/articlerender.fcgi?tool=pmcentrez&artid=1664679','PMC'); return false;" href="https://www.pubmedcentral.nih.gov/articlerender.fcgi?tool=pmcentrez&artid=1664679"><span>The carbon cycle on early Earth—and on Mars?</span></a></p> <p><a target="_blank" rel="noopener noreferrer" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?DB=pmc">PubMed Central</a></p> <p>Grady, Monica M; Wright, Ian</p> <p>2006-01-01</p> <p>One of the goals of the present Martian exploration is to search for evidence of extinct (or even extant) life. This could be redefined as a search for carbon. The carbon cycle (or, more properly, cycles) on Earth is a complex interaction among three reservoirs: the atmosphere; the hydrosphere; and the lithosphere. Superimposed on this is the biosphere, and its presence influences the fixing and release of carbon in these reservoirs over different time-scales. The overall carbon balance is kept at equilibrium on the surface by a combination of tectonic processes (which bury carbon), volcanism (which releases it) and biology (which mediates it). In contrast to Earth, Mars presently has no active tectonic system; neither does it possess a significant biosphere. However, these observations might not necessarily have held in the past. By looking at how Earth's carbon cycles have changed with time, as both the Earth's tectonic structure and a more sophisticated biology have evolved, and also by constructing a carbon cycle for Mars based on the carbon chemistry of Martian meteorites, we investigate whether or not there is evidence for a Martian biosphere. PMID:17008211</p> </li> <li> <p><a target="_blank" rel="noopener noreferrer" onclick="trackOutboundLink('http://adsabs.harvard.edu/abs/2016AGUFMGC23K..17H','NASAADS'); return false;" href="http://adsabs.harvard.edu/abs/2016AGUFMGC23K..17H"><span>The future of the North American carbon cycle - projections and associated climate change</span></a></p> <p><a target="_blank" rel="noopener noreferrer" href="http://adsabs.harvard.edu/abstract_service.html">NASA Astrophysics Data System (ADS)</a></p> <p>Huntzinger, D. N.; Chatterjee, A.; Cooley, S. R.; Dunne, J. P.; Hoffman, F. M.; Luo, Y.; Moore, D. J.; Ohrel, S. B.; Poulter, B.; Ricciuto, D. M.; Tzortziou, M.; Walker, A. P.; Mayes, M. A.</p> <p>2016-12-01</p> <p>Approximately half of anthropogenic emissions from the burning of fossil fuels is taken up annually by carbon sinks on the land and in the oceans. However, there are key uncertainties in how carbon uptake by terrestrial, ocean, and freshwater systems will respond to, and interact with, climate into the future. Here, we outline the current state of understanding on the future carbon budget of these major reservoirs within North America and the globe. We examine the drivers of future carbon cycle changes, including carbon-climate feedbacks, atmospheric composition, nutrient availability, and human activity and management decisions. Progress has been made at identifying vulnerabilities in carbon pools, including high-latitude permafrost, peatlands, freshwater and coastal wetlands, and ecosystems subject to disturbance events, such as insects, fire and drought. However, many of these processes/pools are not well represented in current models, and model intercomparison studies have shown a range in carbon cycle response to factors such as climate and CO2 fertilization. Furthermore, as model complexity increases, understanding the drivers of model spread becomes increasingly more difficult. As a result, uncertainties in future carbon cycle projections are large. It is also uncertain how management decisions and policies will impact future carbon stocks and flows. In order to guide policy, a better understanding of the risk and magnitude of North American carbon cycle changes is needed. This requires that future carbon cycle projections be conditioned on current observations and be reported with sufficient confidence and fully specified uncertainties.</p> </li> <li> <p><a target="_blank" rel="noopener noreferrer" onclick="trackOutboundLink('https://www.fs.usda.gov/treesearch/pubs/38756','TREESEARCH'); return false;" href="https://www.fs.usda.gov/treesearch/pubs/38756"><span>The changing global carbon cycle: linking local plant-soil carbon dynamics to global consequences</span></a></p> <p><a target="_blank" rel="noopener noreferrer" href="http://www.fs.usda.gov/treesearch/">Treesearch</a></p> <p>F. Stuart Chapin; Jack McFarland; A. David McGuire; Eugenie S. Euskirchen; Roger W. Ruess; Knut Kielland</p> <p>2009-01-01</p> <p>Most current climate-carbon cycle models that include the terrestrial carbon (C) cycle are based on a model developed 40 years ago by Woodwell & Whittaker (1968) and omit advances in biogeochemical understanding since that time. Their model treats net C emissions from ecosystems as the balance between net primary production (NPP) and heterotrophic respiration (HR,...</p> </li> <li> <p><a target="_blank" rel="noopener noreferrer" onclick="trackOutboundLink('https://www.ncbi.nlm.nih.gov/pubmed/29713697','PUBMED'); return false;" href="https://www.ncbi.nlm.nih.gov/pubmed/29713697"><span>Ultra-long-term cycling stability of an integrated carbon-sulfur membrane with dual shuttle-inhibiting layers of graphene "nets" and a porous carbon skin.</span></a></p> <p><a target="_blank" rel="noopener noreferrer" href="https://www.ncbi.nlm.nih.gov/entrez/query.fcgi?DB=pubmed">PubMed</a></p> <p>Liu, Mingkai; Meng, Qinghua; Yang, Zhiyuan; Zhao, Xinsheng; Liu, Tianxi</p> <p>2018-05-15</p> <p>An integrated carbon-sulfur (CSG/PC) membrane with dual shuttle-inhibiting layers was prepared by inserting graphene "nets" and a porous carbon (PC) skin, and the membrane achieved an extraordinary cycling stability up to 1000 cycles with an average Coulombic efficiency of ∼100%.</p> </li> </ol> <div class="pull-right"> <ul class="pagination"> <li><a href="#" onclick='return showDiv("page_1");'>«</a></li> <li><a href="#" onclick='return showDiv("page_17");'>17</a></li> <li><a href="#" onclick='return showDiv("page_18");'>18</a></li> <li class="active"><span>19</span></li> <li><a href="#" onclick='return showDiv("page_20");'>20</a></li> <li><a href="#" onclick='return showDiv("page_21");'>21</a></li> <li><a href="#" onclick='return showDiv("page_25");'>»</a></li> </ul> </div> </div><!-- col-sm-12 --> </div><!-- row --> </div><!-- page_19 --> <div id="page_20" class="hiddenDiv"> <div class="row"> <div class="col-sm-12"> <div class="pull-right"> <ul class="pagination"> <li><a href="#" onclick='return showDiv("page_1");'>«</a></li> <li><a href="#" onclick='return showDiv("page_18");'>18</a></li> <li><a href="#" onclick='return showDiv("page_19");'>19</a></li> <li class="active"><span>20</span></li> <li><a href="#" onclick='return showDiv("page_21");'>21</a></li> <li><a href="#" onclick='return showDiv("page_22");'>22</a></li> <li><a href="#" onclick='return showDiv("page_25");'>»</a></li> </ul> </div> </div> </div> <div class="row"> <div class="col-sm-12"> <ol class="result-class" start="381"> <li> <p><a target="_blank" rel="noopener noreferrer" onclick="trackOutboundLink('https://www.osti.gov/biblio/1326148-spatial-patterns-environmental-controls-particulate-organic-carbon-surface-waters-conterminous-united-states','SCIGOV-STC'); return false;" href="https://www.osti.gov/biblio/1326148-spatial-patterns-environmental-controls-particulate-organic-carbon-surface-waters-conterminous-united-states"><span>Spatial patterns and environmental controls of particulate organic carbon in surface waters in the conterminous United States</span></a></p> <p><a target="_blank" rel="noopener noreferrer" href="http://www.osti.gov/search">DOE Office of Scientific and Technical Information (OSTI.GOV)</a></p> <p>Yang, Qichun; Zhang, Xuesong; Xu, Xingya</p> <p>2016-06-01</p> <p>Carbon stocks and fluxes in inland waters have been identified as important, but poorly constrained components of the global carbon cycle. In this study, we compile and analyze particulate organic carbon (POC) concentration data from 1145 U.S. Geological Survey (USGS) hydrologic stations to investigate the spatial variability and environmental controls of POC concentration. We observe substantial spatial variability in POC concentration (1.43 ± 2.56 mg C/ L, Mean ± Standard Deviation), with the Upper Mississippi River basin and the Piedmont region in the eastern U.S. having the highest POC concentration. Further, we employ generalized linear regression models to analyze themore » impacts of sediment transport and algae growth as well as twenty-one other environmental factors on the POC variability. Suspended sediment and chlorophyll-a explain 26% and 17% of the variability in POC concentration, respectively. At the national level, the twenty-one selected environmental factors combined can explain ca. 40% of the spatial variance in POC concentration. Overall, urban area and soil clay content show significant negative correlation with POC concentration, while soil water content and soil bulk density correlate positively with POC. In addition, total phosphorus concentration and dam density covariate positively with POC concentration. Furthermore, regional scale analyses reveal substantial variation in environmental controls determining POC concentration across the 18 major water resource regions in the U.S. The POC concentration and associated environmental controls also vary non-monotonically with river order. These findings indicate complex interactions among multiple factors in regulating POC production over different spatial scales and across various sections of the river networks. This complexity together with the large unexplained uncertainty highlight the need for consideration of non-linear processes that control them and developing appropriate methodologies to track the transformation and transport of carbon in these terrestrial-aquatic systems. Such scientific advancements will also benefit greatly the Earth system models that are currently deficient in representing properly this component of global carbon cycle.« less</p> </li> <li> <p><a target="_blank" rel="noopener noreferrer" onclick="trackOutboundLink('http://adsabs.harvard.edu/abs/2017AGUFMGC14A..03C','NASAADS'); return false;" href="http://adsabs.harvard.edu/abs/2017AGUFMGC14A..03C"><span>The 2015-2016 El Niño and the response of the carbon cycle: Findings from the Orbiting Carbon Observatory-2 (OCO-2) mission</span></a></p> <p><a target="_blank" rel="noopener noreferrer" href="http://adsabs.harvard.edu/abstract_service.html">NASA Astrophysics Data System (ADS)</a></p> <p>Chatterjee, A.; Schimel, D.; Stephens, B. B.; Crisp, D.; Eldering, A.; Gunson, M. R.; Feely, R. A.; Gierach, M. M.; Keeling, R. F.; Sutton, A. J.; Weir, B.</p> <p>2017-12-01</p> <p>The El Nino Southern Oscillation (ENSO) is the most important mode of tropical climate variability on interannual to decadal time scales. Correlations between atmospheric CO2 growth rate and ENSO activity are relatively well known but the magnitude of this correlation, the contribution from tropical marine vs. terrestrial flux components, and the causal mechanisms, are poorly constrained in space and time. The launch of NASA's Orbiting Carbon Observatory-2 (OCO-2) mission in July 2014 was rather timely given the development of strong ENSO conditions over the tropical Pacific Ocean in 2015-2016. In this presentation, we will discuss how the high-density observations from OCO-2 provided us with a novel dataset to resolve the linkages between El Niño and atmospheric CO2. Along with information from in situ observations of ΔpCO2 from NOAA's Tropical Atmosphere Ocean (TAO) project and atmospheric CO2 from the Scripps CO2 Program, and other remote-sensing missions, we are able to piece together the time dependent response of atmospheric CO2 concentrations over the Tropics. Our findings confirm the hypothesis from studies following the 1997-1998 El Niño event that an early reduction in CO2 outgassing from the tropical Pacific Ocean is later reversed by enhanced net CO2 emissions from the terrestrial biosphere. This implies that a component of the interannual variability (IAV) in the growth rate of atmospheric CO2, which has typically been used to constrain the climate sensitivity of tropical land carbon fluxes, is strongly influenced and modified by ocean fluxes during the early phase of the ENSO event. Our analyses shed further light on the understanding of the marine vs. terrestrial partitioning of tropical carbon fluxes during El Niño events, their relative contributions to the global atmospheric CO2 growth rate, and provide clues about the sensitivity of the carbon cycle to climate forcing on interannual time scales.</p> </li> <li> <p><a target="_blank" rel="noopener noreferrer" onclick="trackOutboundLink('https://www.ncbi.nlm.nih.gov/pubmed/26716292','PUBMED'); return false;" href="https://www.ncbi.nlm.nih.gov/pubmed/26716292"><span>Facile Synthesis of Pre-Doping Lithium-Ion Into Nitrogen-Doped Graphite Negative Electrode for Lithium-Ion Capacitor.</span></a></p> <p><a target="_blank" rel="noopener noreferrer" href="https://www.ncbi.nlm.nih.gov/entrez/query.fcgi?DB=pubmed">PubMed</a></p> <p>Lee, Seul-Yi; Kim, Ji-Il; Rhee, Kyong Yop; Park, Soo-Jin</p> <p>2015-09-01</p> <p>Nitrogen-doped graphite, prepared via the thermal decomposition of melamine into a carbon matrix for use as the negative electrode in lithium-ion capacitors (LICs), was evaluated by electrochemical measurements. Furthermore, in order to study the performance of pre-doped lithium components as a function of nitrogen-doped material, the pre-doped lithium graphite was allowed to react with a lithium salt solution. The results showed that the nitrogen functional groups in the graphite largely influenced the pre-doped lithium components, thereby contributing to the discharge capacity and cycling performance. We confirmed that the large initial irreversible capacity could be significantly decreased by using pre-doped lithium components obtained through the nitrogen-doping method.</p> </li> <li> <p><a target="_blank" rel="noopener noreferrer" onclick="trackOutboundLink('https://www.pubmedcentral.nih.gov/articlerender.fcgi?tool=pmcentrez&artid=1797957','PMC'); return false;" href="https://www.pubmedcentral.nih.gov/articlerender.fcgi?tool=pmcentrez&artid=1797957"><span>Mutations in Alternative Carbon Utilization Pathways in Candida albicans Attenuate Virulence and Confer Pleiotropic Phenotypes▿</span></a></p> <p><a target="_blank" rel="noopener noreferrer" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?DB=pmc">PubMed Central</a></p> <p>Ramírez, Melissa A.; Lorenz, Michael C.</p> <p>2007-01-01</p> <p>The interaction between Candida albicans and cells of the innate immune system is a key determinant of disease progression. Transcriptional profiling has revealed that C. albicans has a complex response to phagocytosis, much of which is similar to carbon starvation. This suggests that nutrient limitation is a significant stress in vivo, and we have shown that glyoxylate cycle mutants are less virulent in mice. To examine whether other aspects of carbon metabolism are important in vivo during an infection, we have constructed strains lacking FOX2 and FBP1, which encode key components of fatty acid β-oxidation and gluconeogenesis, respectively. As expected, fox2Δ mutants failed to utilize several fatty acids as carbon sources. Surprisingly, however, these mutants also failed to grow in the presence of several other carbon sources, whose assimilation is independent of β-oxidation, including ethanol and citric acid. Mutants lacking the glyoxylate enzyme ICL1 also had more severe carbon utilization phenotypes than were expected. These results suggest that the regulation of alternative carbon metabolism in C. albicans is significantly different from that in other fungi. In vivo, fox2Δ mutants show a moderate but significant reduction in virulence in a mouse model of disseminated candidiasis, while disruption of the glyoxylate cycle or gluconeogenesis confers a severe attenuation in this model. These data indicate that C. albicans often encounters carbon-poor conditions during growth in the host and that the ability to efficiently utilize multiple nonfermentable carbon sources is a virulence determinant. Consistent with this in vivo requirement, C. albicans uniquely regulates carbon metabolism in a more integrated manner than in Saccharomyces cerevisiae, such that defects in one part of the machinery have wider impacts than expected. These aspects of alternative carbon metabolism may then be useful as targets for therapeutic intervention. PMID:17158734</p> </li> <li> <p><a target="_blank" rel="noopener noreferrer" onclick="trackOutboundLink('https://www.fs.usda.gov/treesearch/pubs/48796','TREESEARCH'); return false;" href="https://www.fs.usda.gov/treesearch/pubs/48796"><span>Interpretation and evaluation of combined measurement techniques for soil CO2 efflux: Discrete surface chambers and continuous soil CO2 concentration probes</span></a></p> <p><a target="_blank" rel="noopener noreferrer" href="http://www.fs.usda.gov/treesearch/">Treesearch</a></p> <p>Diego A. Riveros-Iregui; Brian L. McGlynn; Howard E. Epstein; Daniel L. Welsch</p> <p>2008-01-01</p> <p>Soil CO2 efflux is a large respiratory flux from terrestrial ecosystems and a critical component of the global carbon (C) cycle. Lack of process understanding of the spatiotemporal controls on soil CO2 efflux limits our ability to extrapolate from fluxes measured at point scales to scales useful for corroboration with other ecosystem level measures of C exchange....</p> </li> <li> <p><a target="_blank" rel="noopener noreferrer" onclick="trackOutboundLink('https://www.osti.gov/servlets/purl/1023462','SCIGOV-STC'); return false;" href="https://www.osti.gov/servlets/purl/1023462"><span>Evaluation and Optimization of a Supercritical Carbon Dioxide Power Conversion Cycle for Nuclear Applications</span></a></p> <p><a target="_blank" rel="noopener noreferrer" href="http://www.osti.gov/search">DOE Office of Scientific and Technical Information (OSTI.GOV)</a></p> <p>Edwin A. Harvego; Michael G. McKellar</p> <p>2011-05-01</p> <p>There have been a number of studies involving the use of gases operating in the supercritical mode for power production and process heat applications. Supercritical carbon dioxide (CO2) is particularly attractive because it is capable of achieving relatively high power conversion cycle efficiencies in the temperature range between 550°C and 750°C. Therefore, it has the potential for use with any type of high-temperature nuclear reactor concept, assuming reactor core outlet temperatures of at least 550°C. The particular power cycle investigated in this paper is a supercritical CO2 Recompression Brayton Cycle. The CO2 Recompression Brayton Cycle can be used as eithermore » a direct or indirect power conversion cycle, depending on the reactor type and reactor outlet temperature. The advantage of this cycle when compared to the helium Brayton Cycle is the lower required operating temperature; 550°C versus 850°C. However, the supercritical CO2 Recompression Brayton Cycle requires an operating pressure in the range of 20 MPa, which is considerably higher than the required helium Brayton cycle operating pressure of 8 MPa. This paper presents results of analyses performed using the UniSim process analyses software to evaluate the performance of the supercritical CO2 Brayton Recompression Cycle for different reactor outlet temperatures. The UniSim model assumed a 600 MWt reactor power source, which provides heat to the power cycle at a maximum temperature of between 550°C and 750°C. The UniSim model used realistic component parameters and operating conditions to model the complete power conversion system. CO2 properties were evaluated, and the operating range for the cycle was adjusted to take advantage of the rapidly changing conditions near the critical point. The UniSim model was then optimized to maximize the power cycle thermal efficiency at the different maximum power cycle operating temperatures. The results of the analyses showed that power cycle thermal efficiencies in the range of 40 to 50% can be achieved.« less</p> </li> <li> <p><a target="_blank" rel="noopener noreferrer" onclick="trackOutboundLink('https://www.osti.gov/servlets/purl/864351','DOE-PATENT-XML'); return false;" href="https://www.osti.gov/servlets/purl/864351"><span>Cyclic process for producing methane from carbon monoxide with heat removal</span></a></p> <p><a target="_blank" rel="noopener noreferrer" href="http://www.osti.gov/doepatents">DOEpatents</a></p> <p>Frost, Albert C.; Yang, Chang-lee</p> <p>1982-01-01</p> <p>Carbon monoxide-containing gas streams are converted to methane by a cyclic, essentially two-step process in which said carbon monoxide is disproportionated to form carbon dioxide and active surface carbon deposited on the surface of a catalyst, and said carbon is reacted with steam to form product methane and by-product carbon dioxide. The exothermic heat of reaction generated in each step is effectively removed during each complete cycle so as to avoid a build up of heat from cycle-to-cycle, with particularly advantageous techniques being employed for fixed bed, tubular and fluidized bed reactor operations.</p> </li> <li> <p><a target="_blank" rel="noopener noreferrer" onclick="trackOutboundLink('http://www.osti.gov/sciencecinema/biblio/987901','SCIGOVIMAGE-SCICINEMA'); return false;" href="http://www.osti.gov/sciencecinema/biblio/987901"><span>Carbon Cycle 2.0: Paul Alivisatos: Introduction</span></a></p> <p><a target="_blank" rel="noopener noreferrer" href="http://www.osti.gov/sciencecinema/">ScienceCinema</a></p> <p>Paul Alivisatos</p> <p>2017-12-09</p> <p>Berkeley Lab Director Paul Alivisatos speaks at the Carbon Cycle 2.0 kick-off symposium Feb. 1, 2010. Humanity emits more carbon into the atmosphere than natural processes are able to remove - an imbalance with negative consequences.Carbon Cycle 2.0 is a Berkeley Lab initiative to provide the science needed to restore this balance by integrating the Labs diverse research activities and delivering creative solutions toward a carbon-neutral energy future. http://carboncycle2.lbl.gov/</p> </li> <li> <p><a target="_blank" rel="noopener noreferrer" onclick="trackOutboundLink('http://www.osti.gov/sciencecinema/biblio/987899','SCIGOVIMAGE-SCICINEMA'); return false;" href="http://www.osti.gov/sciencecinema/biblio/987899"><span>Carbon Cycle 2.0: Mary Ann Piette: Impact of efficient buildings</span></a></p> <p><a target="_blank" rel="noopener noreferrer" href="http://www.osti.gov/sciencecinema/">ScienceCinema</a></p> <p>Mary Ann Piette</p> <p>2017-12-09</p> <p>Mary Ann Piette speaks at the Carbon Cycle 2.0 kick-off symposium Feb. 2, 2010. We emit more carbon into the atmosphere than natural processes are able to remove - an imbalance with negative consequences. Carbon Cycle 2.0 is a Berkeley Lab initiative to provide the science needed to restore this balance by integrating the Labs diverse research activities and delivering creative solutions toward a carbon-neutral energy future. http://carboncycle2.lbl.gov/</p> </li> <li> <p><a target="_blank" rel="noopener noreferrer" onclick="trackOutboundLink('http://www.osti.gov/sciencecinema/biblio/987895','SCIGOVIMAGE-SCICINEMA'); return false;" href="http://www.osti.gov/sciencecinema/biblio/987895"><span>Carbon Cycle 2.0: Bill Collins: A future without CC2.0</span></a></p> <p><a target="_blank" rel="noopener noreferrer" href="http://www.osti.gov/sciencecinema/">ScienceCinema</a></p> <p>Bill Collins</p> <p>2017-12-09</p> <p>Bill Collins speaks at the Carbon Cycle 2.0 kick-off symposium Feb. 1, 2010. We emit more carbon into the atmosphere than natural processes are able to remove - an imbalance with negative consequences. Carbon Cycle 2.0 is a Berkeley Lab initiative to provide the science needed to restore this balance by integrating the Labs diverse research activities and delivering creative solutions toward a carbon-neutral energy future. http://carboncycle2.lbl.gov/</p> </li> <li> <p><a target="_blank" rel="noopener noreferrer" onclick="trackOutboundLink('https://www.osti.gov/servlets/purl/987899','SCIGOV-STC'); return false;" href="https://www.osti.gov/servlets/purl/987899"><span>Carbon Cycle 2.0: Mary Ann Piette: Impact of efficient buildings</span></a></p> <p><a target="_blank" rel="noopener noreferrer" href="http://www.osti.gov/search">DOE Office of Scientific and Technical Information (OSTI.GOV)</a></p> <p>Mary Ann Piette</p> <p></p> <p>Mary Ann Piette speaks at the Carbon Cycle 2.0 kick-off symposium Feb. 2, 2010. We emit more carbon into the atmosphere than natural processes are able to remove - an imbalance with negative consequences. Carbon Cycle 2.0 is a Berkeley Lab initiative to provide the science needed to restore this balance by integrating the Labs diverse research activities and delivering creative solutions toward a carbon-neutral energy future. http://carboncycle2.lbl.gov/</p> </li> <li> <p><a target="_blank" rel="noopener noreferrer" onclick="trackOutboundLink('https://www.osti.gov/servlets/purl/987895','SCIGOV-STC'); return false;" href="https://www.osti.gov/servlets/purl/987895"><span>Carbon Cycle 2.0: Bill Collins: A future without CC2.0</span></a></p> <p><a target="_blank" rel="noopener noreferrer" href="http://www.osti.gov/search">DOE Office of Scientific and Technical Information (OSTI.GOV)</a></p> <p>Bill Collins</p> <p>2010-02-09</p> <p>Bill Collins speaks at the Carbon Cycle 2.0 kick-off symposium Feb. 1, 2010. We emit more carbon into the atmosphere than natural processes are able to remove - an imbalance with negative consequences. Carbon Cycle 2.0 is a Berkeley Lab initiative to provide the science needed to restore this balance by integrating the Labs diverse research activities and delivering creative solutions toward a carbon-neutral energy future. http://carboncycle2.lbl.gov/</p> </li> <li> <p><a target="_blank" rel="noopener noreferrer" onclick="trackOutboundLink('https://www.osti.gov/servlets/purl/987901','SCIGOV-STC'); return false;" href="https://www.osti.gov/servlets/purl/987901"><span>Carbon Cycle 2.0: Paul Alivisatos: Introduction</span></a></p> <p><a target="_blank" rel="noopener noreferrer" href="http://www.osti.gov/search">DOE Office of Scientific and Technical Information (OSTI.GOV)</a></p> <p>Paul Alivisatos</p> <p>2010-02-09</p> <p>Berkeley Lab Director Paul Alivisatos speaks at the Carbon Cycle 2.0 kick-off symposium Feb. 1, 2010. Humanity emits more carbon into the atmosphere than natural processes are able to remove - an imbalance with negative consequences.Carbon Cycle 2.0 is a Berkeley Lab initiative to provide the science needed to restore this balance by integrating the Labs diverse research activities and delivering creative solutions toward a carbon-neutral energy future. http://carboncycle2.lbl.gov/</p> </li> <li> <p><a target="_blank" rel="noopener noreferrer" onclick="trackOutboundLink('http://adsabs.harvard.edu/abs/2018SMaS...27g4002D','NASAADS'); return false;" href="http://adsabs.harvard.edu/abs/2018SMaS...27g4002D"><span>High-cycle electromechanical aging of dielectric elastomer actuators with carbon-based electrodes</span></a></p> <p><a target="_blank" rel="noopener noreferrer" href="http://adsabs.harvard.edu/abstract_service.html">NASA Astrophysics Data System (ADS)</a></p> <p>de Saint-Aubin, C. A.; Rosset, S.; Schlatter, S.; Shea, H.</p> <p>2018-07-01</p> <p>We present high-cycle aging tests of dielectric elastomer actuators (DEAs) based on silicone elastomers, reporting on the time-evolution of actuation strain and of electrode resistance over millions of cycles. We compare several types of carbon-based electrodes, and for the first time show how the choice of electrode has a dramatic influence on DEA aging. An expanding circle DEA configuration is used, consisting of a commercial silicone membrane with the following electrodes: commercial carbon grease applied manually, solvent-diluted carbon grease applied by stamping (pad printing), loose carbon black powder applied manually, carbon black powder suspension applied by inkjet-printing, and conductive silicone-carbon composite applied by stamping. The silicone-based DEAs with manually applied carbon grease electrodes show the shortest lifetime of less than 105 cycles at 5% strain, while the inkjet-printed carbon powder and the stamped silicone-carbon composite make for the most reliable devices, with lifetimes greater than 107 cycles at 5% strain. These results are valid for the specific dielectric and electrode configurations that were tested: using other dielectrics or electrode formulations would lead to different lifetimes and failure modes. We find that aging (as seen in the change in resistance and in actuation strain versus cycle number) is independent of the actuation frequency from 10 Hz to 200 Hz, and depends on the total accumulated time the DEA spends in an actuated state.</p> </li> <li> <p><a target="_blank" rel="noopener noreferrer" onclick="trackOutboundLink('http://adsabs.harvard.edu/abs/2010AGUFMPP31C1639R','NASAADS'); return false;" href="http://adsabs.harvard.edu/abs/2010AGUFMPP31C1639R"><span>Carbon Cycle Dynamics through the Early Eocene Climatic Optimum: Orbital Couplings to Lacustrine Cycling</span></a></p> <p><a target="_blank" rel="noopener noreferrer" href="http://adsabs.harvard.edu/abstract_service.html">NASA Astrophysics Data System (ADS)</a></p> <p>Rosengard, S. Z.; Grogan, D. S.; Whiteside, J. H.; van Keuren, M.; Musher, D.</p> <p>2010-12-01</p> <p>The early Eocene represents the most recent hothouse climate state of Earth history, a period during which Earth’s surface temperatures warmed and reached a steady peak at the Early Eocene Climatic Optimum (EECO), 53.5-50 Ma. Interspersed through the primary warming interval were several hyperthermals, or rapid peaks in surface temperature and pulses of carbon dioxide into the atmosphere, followed by rapid declines, lasting 10^4 to 10^5 years. Various hypotheses have been offered to explain the climatic triggers during the hothouse interval, including changes in ocean circulation, methane release from hydrates, volcanism, and turnover of terrestrial organic matter, implicating various couplings and feedbacks in the global carbon cycle. The present study investigates the prevailing changes in carbon cycle dynamics that occurred during a specific subinterval of the Early Eocene Climatic Optimum. We sampled a carbon-rich 300-ft ( 1100 kyr) section of lacustrine Green River Formation sediments from the TOSCO core in the Uinta Basin at a one-foot resolution for organic carbon content and δ^{13}C. The compiled data comprise a high-resolution profile of total organic carbon and isotopic organic carbon composition through the section, showing cyclic patterns that we hypothesize reflect orbital signals. Bulk isotopic carbon and shale oil measurements from an earlier Fischer Assay across TOSCO’s entire 1030-ft core were then filtered using the expected frequency of a 23-kyr precession cycle. The overlaid cycles reveal δ^{13}C and oil content to be anti-phase through the 300-ft section, except for an interval of 50 feet (180 kyr) from the Mahogany Zone to the B-groove of the core, where the two measurements are in-phase. Given that shale oil, a proxy for lake primary productivity and carbon burial, and δ^{13}C typically correlate inversely, this short, 180-kyr interval of in-phase variation suggests a significant alteration in the local carbon cycle. These preliminary findings reveal a dynamic, inconstant coupling between precessional variations in solar insolation and the carbon cycle during the EECO. As the organic carbon profile fundamentally records ecosystem processes, this precession-carbon cycle coupling is likely modulated by ecological dynamics within the paleolake, such as changing trophic and community structure. Because precession-driven changes in solar insolation dominantly control hydrology and lake water balance, the lacustrine ecosystem response to such perturbations may have precipitated key shifts in the dynamics of carbon cycling through the most stable interval of Earth’s latest hothouse.</p> </li> <li> <p><a target="_blank" rel="noopener noreferrer" onclick="trackOutboundLink('https://www.osti.gov/biblio/1170462-metaproteomics-reveals-differential-modes-metabolic-coupling-among-ubiquitous-oxygen-minimum-zone-microbes','SCIGOV-STC'); return false;" href="https://www.osti.gov/biblio/1170462-metaproteomics-reveals-differential-modes-metabolic-coupling-among-ubiquitous-oxygen-minimum-zone-microbes"><span>Metaproteomics reveals differential modes of metabolic coupling among ubiquitous oxygen minimum zone microbes</span></a></p> <p><a target="_blank" rel="noopener noreferrer" href="http://www.osti.gov/search">DOE Office of Scientific and Technical Information (OSTI.GOV)</a></p> <p>Hawley, Alyse K.; Brewer, Heather M.; Norbeck, Angela D.</p> <p>2014-08-05</p> <p>Oxygen minimum zones (OMZs) are intrinsic water column features arising from respiratory oxygen demand during organic matter degradation in stratified marine waters. Currently OMZs are expanding due to global climate change. This expansion alters marine ecosystem function and the productivity of fisheries due to habitat compression and changes in biogeochemical cycling leading to fixed nitrogen loss and greenhouse gas production. Here we use metaproteomics to chart spatial and temporal patterns of gene expression along defined redox gradients in a seasonally anoxic fjord, Saanich Inlet to better understand microbial community responses to OMZ expansion. The expression of metabolic pathway components formore » nitrification, anaerobic ammonium oxidation (anammox), denitrification and inorganic carbon fixation predominantly co-varied with abundance and distribution patterns of Thaumarchaeota, Nitrospira, Planctomycetes and SUP05/ARCTIC96BD-19 Gammaproteobacteria. Within these groups, pathways mediating inorganic carbon fixation and nitrogen and sulfur transformations were differentially expressed across the redoxcline. Nitrification and inorganic carbon fixation pathways affiliated with Thaumarchaeota dominated dysoxic waters and denitrification, sulfur-oxidation and inorganic carbon fixation pathways affiliated with SUP05 dominated suboxic and anoxic waters. Nitrite-oxidation and anammox pathways affiliated with Nitrospina and Planctomycetes respectively, also exhibited redox partitioning between dysoxic and suboxic waters. The differential expression of these pathways under changing water column redox conditions has quantitative implications for coupled biogeochemical cycling linking different modes of inorganic carbon fixation with distributed nitrogen and sulfur-based energy metabolism extensible to coastal and open ocean OMZs.« less</p> </li> <li> <p><a target="_blank" rel="noopener noreferrer" onclick="trackOutboundLink('https://ntrs.nasa.gov/search.jsp?R=20040112537&hterms=bacterias&qs=Ntx%3Dmode%2Bmatchall%26Ntk%3DAll%26N%3D0%26No%3D60%26Ntt%3Dbacterias','NASA-TRS'); return false;" href="https://ntrs.nasa.gov/search.jsp?R=20040112537&hterms=bacterias&qs=Ntx%3Dmode%2Bmatchall%26Ntk%3DAll%26N%3D0%26No%3D60%26Ntt%3Dbacterias"><span>Autotrophy of green non-sulphur bacteria in hot spring microbial mats: biological explanations for isotopically heavy organic carbon in the geological record</span></a></p> <p><a target="_blank" rel="noopener noreferrer" href="http://ntrs.nasa.gov/search.jsp">NASA Technical Reports Server (NTRS)</a></p> <p>van der Meer, M. T.; Schouten, S.; de Leeuw, J. W.; Ward, D. M.</p> <p>2000-01-01</p> <p>Inferences about the evidence of life recorded in organic compounds within the Earth's ancient rocks have depended on 13C contents low enough to be characteristic of biological debris produced by the well-known CO2 fixation pathway, the Calvin cycle. 'Atypically' high values have been attributed to isotopic alteration of sedimentary organic carbon by thermal metamorphism. We examined the possibility that organic carbon characterized by a relatively high 13C content could have arisen biologically from recently discovered autotrophic pathways. We focused on the green non-sulphur bacterium Chloroflexus aurantiacus that uses the 3-hydroxypropionate pathway for inorganic carbon fixation and is geologically significant as it forms modern mat communities analogous to stromatolites. Organic matter in mats constructed by Chloroflexus spp. alone had relatively high 13C contents (-14.9%) and lipids diagnostic of Chloroflexus that were also isotopically heavy (-8.9% to -18.5%). Organic matter in mats constructed by Chloroflexus in conjunction with cyanobacteria had a more typical Calvin cycle signature (-23.5%). However, lipids diagnostic of Chloroflexus were isotopically enriched (-15.1% to -24.1%) relative to lipids typical of cyanobacteria (-33.9% to -36.3%). This suggests that, in mats formed by both cyanobacteria and Chloroflexus, autotrophy must have a greater effect on Chloroflexus carbon metabolism than the photoheterotrophic consumption of cyanobacterial photosynthate. Chloroflexus cell components were also selectively preserved. Hence, Chloroflexus autotrophy and selective preservation of its products constitute one purely biological mechanism by which isotopically heavy organic carbon could have been introduced into important Precambrian geological features.</p> </li> <li> <p><a target="_blank" rel="noopener noreferrer" onclick="trackOutboundLink('https://www.ncbi.nlm.nih.gov/pubmed/22054590','PUBMED'); return false;" href="https://www.ncbi.nlm.nih.gov/pubmed/22054590"><span>Feasibility of CO₂/SO₂ uptake enhancement of calcined limestone modified with rice husk ash during pressurized carbonation.</span></a></p> <p><a target="_blank" rel="noopener noreferrer" href="https://www.ncbi.nlm.nih.gov/entrez/query.fcgi?DB=pubmed">PubMed</a></p> <p>Chen, Huichao; Zhao, Changsui; Ren, Qiangqiang</p> <p>2012-01-01</p> <p>The calcination/carbonation cycle using calcium-based sorbents appears to be a viable method for carbon dioxide (CO₂) capture from combustion gases. Recent attempts to improve the CO₂/SO₂ uptake of a calcium-based sorbent modified by using rice husk ash (RHA) in the hydration process have succeeded in enhancing its effectiveness. The optimal mole ratio of RHA to calcined limestone (M(Si/Ca)) was adjusted to 0.2. The cyclic CO₂ capture characteristics and the SO₂ uptake activity of the modified sorbent were evaluated in a calcination/pressurized carbonation reactor system. Scanning electron microscope (SEM) images and X-ray diffraction (XRD) spectrum of the sorbent were also taken to supplement the study. The results showed that the carbonation conversion was greatly increased for the sorbent with M(Si/Ca) ratio of 0.2. For this sorbent formulation the optimal operating conditions were 700-750 °C and 0.5-0.7 MPa. CO₂ absorption was not proportional to CO₂ concentration in the carbonation atmosphere, but was directly related to reaction time. The CO₂ uptake decreased in the presence of SO₂. SO₂ uptake increased, and the total calcium utilization was maintained over multiple cycles. Analysis has shown that the silicate component is evenly or well distributed, and this serves as a framework to prevent sintering, thus preserving the available microstructure for reaction. The sorbent also displayed high activity to SO₂ absorption and could be used to capture CO₂ and SO₂ simultaneously. Copyright © 2011 Elsevier Ltd. All rights reserved.</p> </li> <li> <p><a target="_blank" rel="noopener noreferrer" onclick="trackOutboundLink('https://www.osti.gov/servlets/purl/1398171','SCIGOV-STC'); return false;" href="https://www.osti.gov/servlets/purl/1398171"><span>Molecular and Microscopic Insights into the Formation of Soil Organic Matter in a Red Pine Rhizosphere</span></a></p> <p><a target="_blank" rel="noopener noreferrer" href="http://www.osti.gov/search">DOE Office of Scientific and Technical Information (OSTI.GOV)</a></p> <p>Dohnalkova, Alice C.; Tfaily, Malak M.; Smith, A. Peyton</p> <p></p> <p>Microbially-derived carbon inputs to soils play an important role in forming soil organic matter (SOM), but detailed knowledge of basic mechanisms of carbon (C) cycling, such as stabilization of organic C compounds originating from rhizodeposition, is scarce. This study aimed to investigate the stability of rhizosphere-produced carbon components in a model laboratory mesocosm of Pinus resinosa grown in a designed mineral soil mix with limited nutrients. We utilized a suite of advanced imaging and molecular techniques to obtain a molecular-level identification of newly-formed SOM compounds, and considered implications regarding their degree of long-term persistence. The microbes in this controlled, nutrient-limitedmore » system, without pre-existing organic matter, produced extracellular polymeric substances that formed associations with nutrient-bearing minerals and contributed to the microbial mineral weathering process. Electron microscopy revealed unique ultrastructural residual signatures of biogenic C compounds, and the increased presence of an amorphous organic phase associated with the mineral phase was evidenced by X-ray diffraction. Here, these findings provide insight into the formation of SOM products in ecosystems, and show that the plant- and microbially-derived material associated with mineral matrices may be important components in current soil carbon models.« less</p> </li> <li> <p><a target="_blank" rel="noopener noreferrer" onclick="trackOutboundLink('https://www.osti.gov/pages/biblio/1398171-molecular-microscopic-insights-formation-soil-organic-matter-red-pine-rhizosphere','SCIGOV-DOEP'); return false;" href="https://www.osti.gov/pages/biblio/1398171-molecular-microscopic-insights-formation-soil-organic-matter-red-pine-rhizosphere"><span>Molecular and Microscopic Insights into the Formation of Soil Organic Matter in a Red Pine Rhizosphere</span></a></p> <p><a target="_blank" rel="noopener noreferrer" href="http://www.osti.gov/pages">DOE PAGES</a></p> <p>Dohnalkova, Alice C.; Tfaily, Malak M.; Smith, A. Peyton; ...</p> <p>2017-08-26</p> <p>Microbially-derived carbon inputs to soils play an important role in forming soil organic matter (SOM), but detailed knowledge of basic mechanisms of carbon (C) cycling, such as stabilization of organic C compounds originating from rhizodeposition, is scarce. This study aimed to investigate the stability of rhizosphere-produced carbon components in a model laboratory mesocosm of Pinus resinosa grown in a designed mineral soil mix with limited nutrients. We utilized a suite of advanced imaging and molecular techniques to obtain a molecular-level identification of newly-formed SOM compounds, and considered implications regarding their degree of long-term persistence. The microbes in this controlled, nutrient-limitedmore » system, without pre-existing organic matter, produced extracellular polymeric substances that formed associations with nutrient-bearing minerals and contributed to the microbial mineral weathering process. Electron microscopy revealed unique ultrastructural residual signatures of biogenic C compounds, and the increased presence of an amorphous organic phase associated with the mineral phase was evidenced by X-ray diffraction. Here, these findings provide insight into the formation of SOM products in ecosystems, and show that the plant- and microbially-derived material associated with mineral matrices may be important components in current soil carbon models.« less</p> </li> </ol> <div class="pull-right"> <ul class="pagination"> <li><a href="#" onclick='return showDiv("page_1");'>«</a></li> <li><a href="#" onclick='return showDiv("page_18");'>18</a></li> <li><a href="#" onclick='return showDiv("page_19");'>19</a></li> <li class="active"><span>20</span></li> <li><a href="#" onclick='return showDiv("page_21");'>21</a></li> <li><a href="#" onclick='return showDiv("page_22");'>22</a></li> <li><a href="#" onclick='return showDiv("page_25");'>»</a></li> </ul> </div> </div><!-- col-sm-12 --> </div><!-- row --> </div><!-- page_20 --> <div id="page_21" class="hiddenDiv"> <div class="row"> <div class="col-sm-12"> <div class="pull-right"> <ul class="pagination"> <li><a href="#" onclick='return showDiv("page_1");'>«</a></li> <li><a href="#" onclick='return showDiv("page_19");'>19</a></li> <li><a href="#" onclick='return showDiv("page_20");'>20</a></li> <li class="active"><span>21</span></li> <li><a href="#" onclick='return showDiv("page_22");'>22</a></li> <li><a href="#" onclick='return showDiv("page_23");'>23</a></li> <li><a href="#" onclick='return showDiv("page_25");'>»</a></li> </ul> </div> </div> </div> <div class="row"> <div class="col-sm-12"> <ol class="result-class" start="401"> <li> <p><a target="_blank" rel="noopener noreferrer" onclick="trackOutboundLink('http://adsabs.harvard.edu/abs/2016GMD.....9.2853J','NASAADS'); return false;" href="http://adsabs.harvard.edu/abs/2016GMD.....9.2853J"><span>C4MIP - The Coupled Climate-Carbon Cycle Model Intercomparison Project: experimental protocol for CMIP6</span></a></p> <p><a target="_blank" rel="noopener noreferrer" href="http://adsabs.harvard.edu/abstract_service.html">NASA Astrophysics Data System (ADS)</a></p> <p>Jones, Chris D.; Arora, Vivek; Friedlingstein, Pierre; Bopp, Laurent; Brovkin, Victor; Dunne, John; Graven, Heather; Hoffman, Forrest; Ilyina, Tatiana; John, Jasmin G.; Jung, Martin; Kawamiya, Michio; Koven, Charlie; Pongratz, Julia; Raddatz, Thomas; Randerson, James T.; Zaehle, Sönke</p> <p>2016-08-01</p> <p>Coordinated experimental design and implementation has become a cornerstone of global climate modelling. Model Intercomparison Projects (MIPs) enable systematic and robust analysis of results across many models, by reducing the influence of ad hoc differences in model set-up or experimental boundary conditions. As it enters its 6th phase, the Coupled Model Intercomparison Project (CMIP6) has grown significantly in scope with the design and documentation of individual simulations delegated to individual climate science communities. The Coupled Climate-Carbon Cycle Model Intercomparison Project (C4MIP) takes responsibility for design, documentation, and analysis of carbon cycle feedbacks and interactions in climate simulations. These feedbacks are potentially large and play a leading-order contribution in determining the atmospheric composition in response to human emissions of CO2 and in the setting of emissions targets to stabilize climate or avoid dangerous climate change. For over a decade, C4MIP has coordinated coupled climate-carbon cycle simulations, and in this paper we describe the C4MIP simulations that will be formally part of CMIP6. While the climate-carbon cycle community has created this experimental design, the simulations also fit within the wider CMIP activity, conform to some common standards including documentation and diagnostic requests, and are designed to complement the CMIP core experiments known as the Diagnostic, Evaluation and Characterization of Klima (DECK). C4MIP has three key strands of scientific motivation and the requested simulations are designed to satisfy their needs: (1) pre-industrial and historical simulations (formally part of the common set of CMIP6 experiments) to enable model evaluation, (2) idealized coupled and partially coupled simulations with 1 % per year increases in CO2 to enable diagnosis of feedback strength and its components, (3) future scenario simulations to project how the Earth system will respond to anthropogenic activity over the 21st century and beyond. This paper documents in detail these simulations, explains their rationale and planned analysis, and describes how to set up and run the simulations. Particular attention is paid to boundary conditions, input data, and requested output diagnostics. It is important that modelling groups participating in C4MIP adhere as closely as possible to this experimental design.</p> </li> <li> <p><a target="_blank" rel="noopener noreferrer" onclick="trackOutboundLink('https://www.osti.gov/servlets/purl/1327771','SCIGOV-STC'); return false;" href="https://www.osti.gov/servlets/purl/1327771"><span>C4MIP – The Coupled Climate–Carbon Cycle Model Intercomparison Project: Experimental protocol for CMIP6</span></a></p> <p><a target="_blank" rel="noopener noreferrer" href="http://www.osti.gov/search">DOE Office of Scientific and Technical Information (OSTI.GOV)</a></p> <p>Jones, Chris D.; Arora, Vivek; Friedlingstein, Pierre</p> <p></p> <p>Coordinated experimental design and implementation has become a cornerstone of global climate modelling. Model Intercomparison Projects (MIPs) enable systematic and robust analysis of results across many models, by reducing the influence of ad hoc differences in model set-up or experimental boundary conditions. As it enters its 6th phase, the Coupled Model Intercomparison Project (CMIP6) has grown significantly in scope with the design and documentation of individual simulations delegated to individual climate science communities. The Coupled Climate–Carbon Cycle Model Intercomparison Project (C4MIP) takes responsibility for design, documentation, and analysis of carbon cycle feedbacks and interactions in climate simulations. These feedbacks aremore » potentially large and play a leading-order contribution in determining the atmospheric composition in response to human emissions of CO 2 and in the setting of emissions targets to stabilize climate or avoid dangerous climate change. For over a decade, C4MIP has coordinated coupled climate–carbon cycle simulations, and in this paper we describe the C4MIP simulations that will be formally part of CMIP6. While the climate–carbon cycle community has created this experimental design, the simulations also fit within the wider CMIP activity, conform to some common standards including documentation and diagnostic requests, and are designed to complement the CMIP core experiments known as the Diagnostic, Evaluation and Characterization of Klima (DECK). C4MIP has three key strands of scientific motivation and the requested simulations are designed to satisfy their needs: (1) pre-industrial and historical simulations (formally part of the common set of CMIP6 experiments) to enable model evaluation, (2) idealized coupled and partially coupled simulations with 1 % per year increases in CO 2 to enable diagnosis of feedback strength and its components, (3) future scenario simulations to project how the Earth system will respond to anthropogenic activity over the 21st century and beyond. This study documents in detail these simulations, explains their rationale and planned analysis, and describes how to set up and run the simulations. Particular attention is paid to boundary conditions, input data, and requested output diagnostics. It is important that modelling groups participating in C4MIP adhere as closely as possible to this experimental design.« less</p> </li> <li> <p><a target="_blank" rel="noopener noreferrer" onclick="trackOutboundLink('https://www.osti.gov/pages/biblio/1327771-c4mip-coupled-climatecarbon-cycle-model-intercomparison-project-experimental-protocol-cmip6','SCIGOV-DOEP'); return false;" href="https://www.osti.gov/pages/biblio/1327771-c4mip-coupled-climatecarbon-cycle-model-intercomparison-project-experimental-protocol-cmip6"><span>C4MIP – The Coupled Climate–Carbon Cycle Model Intercomparison Project: Experimental protocol for CMIP6</span></a></p> <p><a target="_blank" rel="noopener noreferrer" href="http://www.osti.gov/pages">DOE PAGES</a></p> <p>Jones, Chris D.; Arora, Vivek; Friedlingstein, Pierre; ...</p> <p>2016-08-25</p> <p>Coordinated experimental design and implementation has become a cornerstone of global climate modelling. Model Intercomparison Projects (MIPs) enable systematic and robust analysis of results across many models, by reducing the influence of ad hoc differences in model set-up or experimental boundary conditions. As it enters its 6th phase, the Coupled Model Intercomparison Project (CMIP6) has grown significantly in scope with the design and documentation of individual simulations delegated to individual climate science communities. The Coupled Climate–Carbon Cycle Model Intercomparison Project (C4MIP) takes responsibility for design, documentation, and analysis of carbon cycle feedbacks and interactions in climate simulations. These feedbacks aremore » potentially large and play a leading-order contribution in determining the atmospheric composition in response to human emissions of CO 2 and in the setting of emissions targets to stabilize climate or avoid dangerous climate change. For over a decade, C4MIP has coordinated coupled climate–carbon cycle simulations, and in this paper we describe the C4MIP simulations that will be formally part of CMIP6. While the climate–carbon cycle community has created this experimental design, the simulations also fit within the wider CMIP activity, conform to some common standards including documentation and diagnostic requests, and are designed to complement the CMIP core experiments known as the Diagnostic, Evaluation and Characterization of Klima (DECK). C4MIP has three key strands of scientific motivation and the requested simulations are designed to satisfy their needs: (1) pre-industrial and historical simulations (formally part of the common set of CMIP6 experiments) to enable model evaluation, (2) idealized coupled and partially coupled simulations with 1 % per year increases in CO 2 to enable diagnosis of feedback strength and its components, (3) future scenario simulations to project how the Earth system will respond to anthropogenic activity over the 21st century and beyond. This study documents in detail these simulations, explains their rationale and planned analysis, and describes how to set up and run the simulations. Particular attention is paid to boundary conditions, input data, and requested output diagnostics. It is important that modelling groups participating in C4MIP adhere as closely as possible to this experimental design.« less</p> </li> <li> <p><a target="_blank" rel="noopener noreferrer" onclick="trackOutboundLink('https://eric.ed.gov/?q=Change+AND+climate&pg=3&id=EJ1160720','ERIC'); return false;" href="https://eric.ed.gov/?q=Change+AND+climate&pg=3&id=EJ1160720"><span>Student Development of Model-Based Reasoning about Carbon Cycling and Climate Change in a Socio-Scientific Issues Unit</span></a></p> <p><a target="_blank" rel="noopener noreferrer" href="http://www.eric.ed.gov/ERICWebPortal/search/extended.jsp?_pageLabel=advanced">ERIC Educational Resources Information Center</a></p> <p>Zangori, Laura; Peel, Amanda; Kinslow, Andrew; Friedrichsen, Patricia; Sadler, Troy D.</p> <p>2017-01-01</p> <p>Carbon cycling is a key natural system that requires robust science literacy to understand how and why climate change is occurring. Studies show that students tend to compartmentalize carbon movement within plants and animals and are challenged to make sense of how carbon cycles on a global scale. Studies also show that students hold faulty models…</p> </li> <li> <p><a target="_blank" rel="noopener noreferrer" onclick="trackOutboundLink('http://adsabs.harvard.edu/abs/2016AGUOS.B11A..04W','NASAADS'); return false;" href="http://adsabs.harvard.edu/abs/2016AGUOS.B11A..04W"><span>The Effect of Temperature on Key Aspects of the Nitrogen Cycle: Comparisons Across Systems</span></a></p> <p><a target="_blank" rel="noopener noreferrer" href="http://adsabs.harvard.edu/abstract_service.html">NASA Astrophysics Data System (ADS)</a></p> <p>Warren, V.</p> <p>2016-02-01</p> <p>The nitrogen cycle sustains life by converting inert di-nitrogen gas (N2) into fixed bio-available forms (e.g. ammonium, nitrate), as well as returning it via gases such as N2 and nitrous oxide (N2O) back into the atmosphere. Recently, the effects of long term warming on key components of the carbon cycle, which is tightly coupled to the nitrogen cycle, have been highlighted but how global warming might systematically affect the balance of the nitrogen cycle is still largely unknown. The effect of long term warming on denitrification and nitrification were investigated using long-term, experimental mesocosm (2006 to present), allowing us to study the effect of warming on natural communities of bacteria involved in these processes. Denitrification activity responded to warming in the short-term in a predictable way, however, long-term moderate warming of 3-5oC (the predicted global increase by the end of the century) increased the specific activity of the sediment and had a pronounced effect on the ratio of N2O to N2. The latter suggesting that with sustained warming, denitrifying bacteria become more efficient at complete denitrification. Molecular analysis of denitrifying communities in our long-term mesocosm experiment also suggested a profound alteration of the communities underlying these differences in process. Similar short-term experiments were carried out on sediments and the water column of the North Eastern Tropical Pacific Oxygen minimum zone (NETP OMZ) including its effect on N2 fixation and here we contrast the findings from those markedly different settings. This research has indicated that we may see similar effects on the nitrogen cycle as we have previously determined in the carbon cycle, with the balance of N-species consumed and created becoming out of balance.</p> </li> <li> <p><a target="_blank" rel="noopener noreferrer" onclick="trackOutboundLink('http://adsabs.harvard.edu/abs/2007AGUFMPP43B1273M','NASAADS'); return false;" href="http://adsabs.harvard.edu/abs/2007AGUFMPP43B1273M"><span>Pleistocene Variations in Delivery and Deposition of Organic Matter Under the Benguela Current Upwelling System - Biomarker Isotopic Evidence From Sediment Light-Dark Color Cycles</span></a></p> <p><a target="_blank" rel="noopener noreferrer" href="http://adsabs.harvard.edu/abstract_service.html">NASA Astrophysics Data System (ADS)</a></p> <p>Meyers, P. A.; Bouloubassi, I.; Pancost, R. D.; Robinson, R. S.</p> <p>2007-12-01</p> <p>The light-dark color cycles that are distinctive features of sediment beneath the Benguela Current Upwelling System imply repetitive alternations in organic matter delivery and deposition. Organic geochemical proxies for paleoproductivity and for depositional conditions were employed to investigate the paleoceanographic processes involved in creating these cycles in two sediment sequences from ODP Site 1084 corresponding to 0.7 and 1.1 Mya. Concentrations of total organic carbon (TOC) vary between 3.5 and 17.1 wt percent, and those of calcium carbonate fluctuate inversely between 68 and 1 percent, suggesting that carbonate dissolution is involved with the light-dark cycles. Bulk organic del 13C and del 15N values that remain constant across the two light-dark sediment intervals indicate that the extent of nutrient utilization did not change in each cycle. Biomarker compositions in both sequences reflect a range of organic matter sources. Abundant n-alkanes and n-alkanols with odd-over-even and even-over-odd distributions, respectively, record land-plant inputs. Other terrestrial biomakers (e.g triterpenoid acids and alcohols) are present but in very low abundances, suggesting that the n- alkyl components derive predominantly from eolian inputs. Carbon isotopic values of n-alkanes range from -25 to -28 permil, suggesting a mixture of C3 and C4 sources. In contrast, n-alkanol isotopic compositions range from -28 to -34 permil, suggesting that they derive solely from C3 plants. Algal biomarkers are abundant and diverse, represented by 1,15-C30 diols (eustigmatophytes), 4-desmethyl and -methylsterols (diatoms, dinoflagellates), and alkenones (haptophytes). These compounds all have del 13C values ranging from ca. -22 to -24 permil, consistent with a marine origin. Systematic differences in isotopic values imply that marine productivity at 1.1 Mya was higher than at 0.7 Mya, but alkenone-based sea-surface temperatures are higher at 1.1 Mya (21 deg) than at 0.7 Mya (15 deg), which indicates that changes in water-mass properties were also involved.</p> </li> <li> <p><a target="_blank" rel="noopener noreferrer" onclick="trackOutboundLink('http://adsabs.harvard.edu/abs/2016AGUFM.B23D0608M','NASAADS'); return false;" href="http://adsabs.harvard.edu/abs/2016AGUFM.B23D0608M"><span>Pyrogenic Carbon as a Nonlinear Driver in the Carbon and Nitrogen Cycles</span></a></p> <p><a target="_blank" rel="noopener noreferrer" href="http://adsabs.harvard.edu/abstract_service.html">NASA Astrophysics Data System (ADS)</a></p> <p>Masiello, C. A.; Silberg, J. J.; Cheng, H. Y.; Gao, X.; Del Valle, I.</p> <p>2016-12-01</p> <p>Our first conceptual models of pyrogenic carbon's effects on the carbon cycle treated this material as a form of organic matter whose environmental residence time was long enough to render it inert, and PyC was modeled as an unreactive mass that moved through C cycle reservoirs essentially unmodified. This concept saw modifications with the recognition that some fractions of PyC were labile. For example, the reactive sugars and lignin monomers cleaved off the lignocellulose matrix by heating have lifetimes on the order of hours to weeks. However, the now-common multiple component model of PyC does not satisfactorily explain many nonlinearities that have been observed when it is added to soils. These nonlinearities include the positive and negative "priming" effects sometimes triggered, where the presence of PyC in some matrices can trigger shifts in the overall microbial community metabolism, as well as alteration of microbial community structure, shifts in the behavior of belowground and aboveground plant parasites, and shifted rates of greenhouse gas emissions that are not well-correlated to shifts in soil hydrologic processes. To understand the effects of PyC on the global C and N cycles, we will need a better understanding of the mechanisms behind PyC-driven C and N cycle nonlinearities. This talk will examine potential mechanisms driving the nonlinearities observed in soil systems following the introduction of PyC. Potential mechanisms discussed will include PyC effects on soil microbial communication and PyC effects on microbial electron transfer. Cell-cell communication through the secretion and detection of small molecules is used by soil microbes to manage many biogeochemically relevant processes including production of biofilms, production of extracellular enzymes, and management of methanogenesis and denitrification. PyC disrupts microbial cell-cell communication differentially, altering some species' ability to communicate more than others. Electron transfer between microbes is a central part of many environmental syntrophies, including those responsible for methanogenesis, and has been shown to be altered by the presence of PyC. Both these processes may underlie observed ecosystem-scale shifts following PyC amendment to soils.</p> </li> <li> <p><a target="_blank" rel="noopener noreferrer" onclick="trackOutboundLink('http://adsabs.harvard.edu/abs/2014BGeo...11.3547C','NASAADS'); return false;" href="http://adsabs.harvard.edu/abs/2014BGeo...11.3547C"><span>Current systematic carbon-cycle observations and the need for implementing a policy-relevant carbon observing system</span></a></p> <p><a target="_blank" rel="noopener noreferrer" href="http://adsabs.harvard.edu/abstract_service.html">NASA Astrophysics Data System (ADS)</a></p> <p>Ciais, P.; Dolman, A. J.; Bombelli, A.; Duren, R.; Peregon, A.; Rayner, P. J.; Miller, C.; Gobron, N.; Kinderman, G.; Marland, G.; Gruber, N.; Chevallier, F.; Andres, R. J.; Balsamo, G.; Bopp, L.; Bréon, F.-M.; Broquet, G.; Dargaville, R.; Battin, T. J.; Borges, A.; Bovensmann, H.; Buchwitz, M.; Butler, J.; Canadell, J. G.; Cook, R. B.; DeFries, R.; Engelen, R.; Gurney, K. R.; Heinze, C.; Heimann, M.; Held, A.; Henry, M.; Law, B.; Luyssaert, S.; Miller, J.; Moriyama, T.; Moulin, C.; Myneni, R. B.; Nussli, C.; Obersteiner, M.; Ojima, D.; Pan, Y.; Paris, J.-D.; Piao, S. L.; Poulter, B.; Plummer, S.; Quegan, S.; Raymond, P.; Reichstein, M.; Rivier, L.; Sabine, C.; Schimel, D.; Tarasova, O.; Valentini, R.; Wang, R.; van der Werf, G.; Wickland, D.; Williams, M.; Zehner, C.</p> <p>2014-07-01</p> <p>A globally integrated carbon observation and analysis system is needed to improve the fundamental understanding of the global carbon cycle, to improve our ability to project future changes, and to verify the effectiveness of policies aiming to reduce greenhouse gas emissions and increase carbon sequestration. Building an integrated carbon observation system requires transformational advances from the existing sparse, exploratory framework towards a dense, robust, and sustained system in all components: anthropogenic emissions, the atmosphere, the ocean, and the terrestrial biosphere. The paper is addressed to scientists, policymakers, and funding agencies who need to have a global picture of the current state of the (diverse) carbon observations. We identify the current state of carbon observations, and the needs and notional requirements for a global integrated carbon observation system that can be built in the next decade. A key conclusion is the substantial expansion of the ground-based observation networks required to reach the high spatial resolution for CO2 and CH4 fluxes, and for carbon stocks for addressing policy-relevant objectives, and attributing flux changes to underlying processes in each region. In order to establish flux and stock diagnostics over areas such as the southern oceans, tropical forests, and the Arctic, in situ observations will have to be complemented with remote-sensing measurements. Remote sensing offers the advantage of dense spatial coverage and frequent revisit. A key challenge is to bring remote-sensing measurements to a level of long-term consistency and accuracy so that they can be efficiently combined in models to reduce uncertainties, in synergy with ground-based data. Bringing tight observational constraints on fossil fuel and land use change emissions will be the biggest challenge for deployment of a policy-relevant integrated carbon observation system. This will require in situ and remotely sensed data at much higher resolution and density than currently achieved for natural fluxes, although over a small land area (cities, industrial sites, power plants), as well as the inclusion of fossil fuel CO2 proxy measurements such as radiocarbon in CO2 and carbon-fuel combustion tracers. Additionally, a policy-relevant carbon monitoring system should also provide mechanisms for reconciling regional top-down (atmosphere-based) and bottom-up (surface-based) flux estimates across the range of spatial and temporal scales relevant to mitigation policies. In addition, uncertainties for each observation data-stream should be assessed. The success of the system will rely on long-term commitments to monitoring, on improved international collaboration to fill gaps in the current observations, on sustained efforts to improve access to the different data streams and make databases interoperable, and on the calibration of each component of the system to agreed-upon international scales.</p> </li> <li> <p><a target="_blank" rel="noopener noreferrer" onclick="trackOutboundLink('http://adsabs.harvard.edu/abs/2014AGUFMPA51A4040M','NASAADS'); return false;" href="http://adsabs.harvard.edu/abs/2014AGUFMPA51A4040M"><span>How Sensitive Is the Carbon Budget Approach to Potential Carbon Cycle Changes?</span></a></p> <p><a target="_blank" rel="noopener noreferrer" href="http://adsabs.harvard.edu/abstract_service.html">NASA Astrophysics Data System (ADS)</a></p> <p>Matthews, D.</p> <p>2014-12-01</p> <p>The recent development of global Earth-system models, which include dynamic representations of both physical climate and carbon cycle processes, has led to new insights about how the climate responds to human carbon dioxide emissions. Notably, several model analyses have now shown that global temperature responds linearly to cumulative CO2 emissions across a wide range of emissions scenarios. This implies that the timing of CO2 emissions does not affect the overall climate response, and allows a finite global carbon carbon budget to be defined for a given global temperature target. This linear climate response, however, emerges from the interaction of several non-linear processes and feedbacks involving how carbon sinks respond to changes in atmospheric CO2 and climate. In this presentation, I will give an overview of how carbon sinks and carbon cycle feedbacks contribute to the overall linearity of the climate response to cumulative emissions, and will assess how robust this relationship is to a range of possible changes in the carbon cycle, including (a) potential positive carbon cycle feedbacks that are not well represented in the current generation of Earth-system models and (b) negative emission scenarios resulting from possible technological strategies to remove CO2 from the atmosphere.</p> </li> <li> <p><a target="_blank" rel="noopener noreferrer" onclick="trackOutboundLink('http://adsabs.harvard.edu/abs/2017NatGe..10..832E','NASAADS'); return false;" href="http://adsabs.harvard.edu/abs/2017NatGe..10..832E"><span>Variability in organic carbon reactivity across lake residence time and trophic gradients</span></a></p> <p><a target="_blank" rel="noopener noreferrer" href="http://adsabs.harvard.edu/abstract_service.html">NASA Astrophysics Data System (ADS)</a></p> <p>Evans, Chris D.; Futter, Martyn N.; Moldan, Filip; Valinia, Salar; Frogbrook, Zoe; Kothawala, Dolly N.</p> <p>2017-11-01</p> <p>The transport of dissolved organic carbon from land to ocean is a large dynamic component of the global carbon cycle. Inland waters are hotspots for organic matter turnover, via both biological and photochemical processes, and mediate carbon transfer between land, oceans and atmosphere. However, predicting dissolved organic carbon reactivity remains problematic. Here we present in situ dissolved organic carbon budget data from 82 predominantly European and North American water bodies with varying nutrient concentrations and water residence times ranging from one week to 700 years. We find that trophic status strongly regulates whether water bodies act as net dissolved organic carbon sources or sinks, and that rates of both dissolved organic carbon production and consumption can be predicted from water residence time. Our results suggest a dominant role of rapid light-driven removal in water bodies with a short water residence time, whereas in water bodies with longer residence times, slower biotic production and consumption processes are dominant and counterbalance one another. Eutrophication caused lakes to transition from sinks to sources of dissolved organic carbon. We conclude that rates and locations of dissolved organic carbon processing and associated CO2 emissions in inland waters may be misrepresented in global carbon budgets if temporal and spatial reactivity gradients are not accounted for.</p> </li> <li> <p><a target="_blank" rel="noopener noreferrer" onclick="trackOutboundLink('http://adsabs.harvard.edu/abs/2016AGUFM.B53A0517S','NASAADS'); return false;" href="http://adsabs.harvard.edu/abs/2016AGUFM.B53A0517S"><span>Automated Monitoring of Carbon Fluxes in a Northern Rocky Mountain Forest Indicates Above-Average Net Primary Productivity During the 2015 Western U.S. Drought</span></a></p> <p><a target="_blank" rel="noopener noreferrer" href="http://adsabs.harvard.edu/abstract_service.html">NASA Astrophysics Data System (ADS)</a></p> <p>Stenzel, J.; Hudiburg, T. W.</p> <p>2016-12-01</p> <p>As global temperatures rise in the 21st century, "hotter" droughts will become more intense and persistent, particularly in areas which already experience seasonal drought. Because forests represent a large and persistent terrestrial carbon sink which has previously offset a significant proportion of anthropogenic carbon emissions, forest carbon cycle responses to drought have become a prominent research concern. However, robust mechanistic modeling of carbon balance responses to projected drought effects requires improved observation-driven representations of carbon cycle processes; many such component processes are rarely monitored in complex terrain, are modeled or unrepresented quantities at eddy covariance sites, or are monitored at course temporal scales that are not conducive to elucidating process responses at process time scales. In the present study, we demonstrate the use of newly available and affordable automated dendrometers for the estimation of intra-seasonal Net Primary Productivity (NPP) in a Northern Rocky Mountain conifer forest which is impacted by seasonal drought. Results from our pilot study suggest that NPP was restricted by mid-summer moisture deficit under the extraordinary 2015 Western U.S. drought, with greater than 90% off stand growth occurring prior to August. Examination of growth on an inter-annual scale, however, suggests that the study site experienced above-average NPP during this exceptionally hot year. Taken together, these findings indicate that intensifying mid-summer drought in regional forests has affected the timing but has not diminished the magnitude of this carbon flux. By employing automated instrumentation for the intra-annual assessment of NPP, we reveal that annual NPP in regional forests is largely determined before mid-summer and is therefore surprisingly resilient to intensities of seasonal drought that exceed normal conditions of the 20th century.</p> </li> <li> <p><a target="_blank" rel="noopener noreferrer" onclick="trackOutboundLink('http://adsabs.harvard.edu/abs/2017AGUFM.B21G2047D','NASAADS'); return false;" href="http://adsabs.harvard.edu/abs/2017AGUFM.B21G2047D"><span>The impact of lianas on the carbon cycle of tropical forests: a modeling study using the Ecosystem Demography model</span></a></p> <p><a target="_blank" rel="noopener noreferrer" href="http://adsabs.harvard.edu/abstract_service.html">NASA Astrophysics Data System (ADS)</a></p> <p>di Porcia e Brugnera, M.; Longo, M.; Verbeek, H.</p> <p>2017-12-01</p> <p>Lianas are an important component of tropical forests, constituting up to 40% of the woody stems and about 35% of the woody species. Tropical forests have been experiencing large-scale structural changes, including an increase in liana abundance and biomass. This may eventually reduce the projected carbon sink of tropical forests. Despite their crucial role no single terrestrial ecosystem model has included lianas so far. Here, we present the very first implementation of lianas in the Ecosystem Demography model (ED2). ED2 is able to represent the competition for water and light between different vegetation types at the regional level. Our new implementation of ED2 is hence suitable to address important questions such as the impact of lianas on the tropical forest carbon balance. We validated the model against forest inventory and eddy covariance flux data at a dry seasonal site (Barro Colorado Island, Panama), and at a wet rainforest site (Paracou, French Guiana). The model was able to represent size structure and carbon accumulation rates. We also evaluated the impact of the unique allocation strategy of lianas on their competitive ability. Lianas invest only a small fraction of their carbon for structural tissues when compared to trees. As a result, lianas benefit from an extra amount of available carbon, however the trade-offs of low allocation on structural tissues are not yet well understood. We are currently investigating a number of hypotheses, including the possibility for lianas to have high turnover rates for leaves and fine roots, or to have high mortality rates due to the loss of structural support when trees die. As such our model allows us to get a better understanding of the role of lianas in the tropical forest carbon cycle.</p> </li> <li> <p><a target="_blank" rel="noopener noreferrer" onclick="trackOutboundLink('https://www.ncbi.nlm.nih.gov/pubmed/28498939','PUBMED'); return false;" href="https://www.ncbi.nlm.nih.gov/pubmed/28498939"><span>Carbon utilization profiles of river bacterial strains facing sole carbon sources suggest metabolic interactions.</span></a></p> <p><a target="_blank" rel="noopener noreferrer" href="https://www.ncbi.nlm.nih.gov/entrez/query.fcgi?DB=pubmed">PubMed</a></p> <p>Goetghebuer, Lise; Servais, Pierre; George, Isabelle F</p> <p>2017-05-01</p> <p>Microbial communities play a key role in water self-purification. They are primary drivers of biogenic element cycles and ecosystem processes. However, these communities remain largely uncharacterized. In order to understand the diversity-heterotrophic activity relationship facing sole carbon sources, we assembled a synthetic community composed of 20 'typical' freshwater bacterial species mainly isolated from the Zenne River (Belgium). The carbon source utilization profiles of each individual strain and of the mixed community were measured in Biolog Phenotype MicroArrays PM1 and PM2A microplates that allowed testing 190 different carbon sources. Our results strongly suggest interactions occurring between our planktonic strains as our synthetic community showed metabolic properties that were not displayed by its single components. Finally, the catabolic performances of the synthetic community and a natural community from the same sampling site were compared. The synthetic community behaved like the natural one and was therefore representative of the latter in regard to carbon source consumption. © FEMS 2017. All rights reserved. For permissions, please e-mail: journals.permissions@oup.com.</p> </li> <li> <p><a target="_blank" rel="noopener noreferrer" onclick="trackOutboundLink('https://www.ncbi.nlm.nih.gov/pubmed/26212607','PUBMED'); return false;" href="https://www.ncbi.nlm.nih.gov/pubmed/26212607"><span>Hindered Glymes for Graphite-Compatible Electrolytes.</span></a></p> <p><a target="_blank" rel="noopener noreferrer" href="https://www.ncbi.nlm.nih.gov/entrez/query.fcgi?DB=pubmed">PubMed</a></p> <p>Shanmukaraj, Devaraj; Grugeon, Sylvie; Laruelle, Stephane; Armand, Michel</p> <p>2015-08-24</p> <p>Organic carbonate mixtures are used almost exclusively as lithium battery electrolyte solvents. The linear compounds (dimethyl carbonate, diethyl carbonate, ethyl methyl carbonate) act mainly as thinner for the more viscous and high-melting ethylene carbonate but are the least stable component and have low flash points; these are serious handicaps for lifetime and safety. Polyethers (glymes) are useful co-solvents, but all formerly known representatives solvate Li(+) strongly enough to co-intercalate in the graphite negative electrode and exfoliate it. We have put forward a new electrolyte composition comprising a polyether to which a bulky tert-butyl group is attached ("hindered glyme"), thus completely preventing co-intercalation while maintaining good conductivity. This alkyl-carbonate-free electrolyte shows remarkable cycle efficiency of the graphite electrode, not only at room temperature, but also at 50 and 70 °C in the presence of lithium bis(fluorosulfonimide). The two-ethylene-bridge hindered glyme has a high boiling point and a flash point of 80 °C, a considerable advantage for safety. © 2015 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.</p> </li> <li> <p><a target="_blank" rel="noopener noreferrer" onclick="trackOutboundLink('https://www.osti.gov/biblio/21187197-carbon-capture-sorption-enhanced-water-gas-shift-reaction-process-using-hydrotalcite-based-material','SCIGOV-STC'); return false;" href="https://www.osti.gov/biblio/21187197-carbon-capture-sorption-enhanced-water-gas-shift-reaction-process-using-hydrotalcite-based-material"><span>Carbon capture by sorption-enhanced water-gas shift reaction process using hydrotalcite-based material</span></a></p> <p><a target="_blank" rel="noopener noreferrer" href="http://www.osti.gov/search">DOE Office of Scientific and Technical Information (OSTI.GOV)</a></p> <p>van Selow, E.R.; Cobden, P.D.; Verbraeken, P.A.</p> <p>2009-05-15</p> <p>A novel route for precombustion decarbonization is the sorption-enhanced water-gas shift (SEWGS) process. In this process carbon dioxide is removed from a synthesis gas at elevated temperature by adsorption. Simultaneously, carbon monoxide is converted to carbon dioxide by the water-gas shift reaction. The periodic adsorption and desorption of carbon dioxide is induced by a pressure swing cycle, and the cyclic capacity can be amplified by purging with steam. From previous studies is it known that for SEWGS applications, hydrotalcite-based materials are particularly attractive as sorbent, and commercial high-temperature shift catalysts can be used for the conversion of carbon monoxide. Tabletsmore » of a potassium promoted hydrotalcite-based material are characterized in both breakthrough and cyclic experiments in a 2 m tall fixed-bed reactor. When exposed to a mixture of carbon dioxide, steam, and nitrogen at 400{sup o}C, the material shows a breakthrough capacity of 1.4 mmol/g. In subsequent experiments the material was mixed with tablets of promoted iron-chromium shift catalyst and exposed to a mixture of carbon dioxide, carbon monoxide, steam, hydrogen, and nitrogen. It is demonstrated that carbon monoxide conversion can be enhanced to 100% in the presence of a carbon dioxide sorbent. At breakthrough, carbon monoxide and carbon dioxide simultaneously appear at the end of the bed. During more than 300 cycles of adsorption/reaction and desorption, the capture rate, and carbon monoxide conversion are confirmed to be stable. Two different cycle types are investigated: one cycle with a CO{sub 2} rinse step and one cycle with a steam rinse step. The performance of both SEWGS cycles are discussed.« less</p> </li> <li> <p><a target="_blank" rel="noopener noreferrer" onclick="trackOutboundLink('http://adsabs.harvard.edu/abs/2018ApSS..443..412X','NASAADS'); return false;" href="http://adsabs.harvard.edu/abs/2018ApSS..443..412X"><span>High performance aqueous symmetric supercapacitors based on advanced carbon electrodes and hydrophilic poly(vinylidene fluoride) porous separator</span></a></p> <p><a target="_blank" rel="noopener noreferrer" href="http://adsabs.harvard.edu/abstract_service.html">NASA Astrophysics Data System (ADS)</a></p> <p>Xie, Qinxing; Huang, Xiaolin; Zhang, Yufeng; Wu, Shihua; Zhao, Peng</p> <p>2018-06-01</p> <p>The main components of a supercapacitor include two electrodes, electrolyte, and a separator, which are all essential to specify the energy storage capability of the device. In this work, two kinds of porous carbon materials have been fabricated via different routes using pomelo peel as raw material. The specific surface area are 1187 m2 g-1 for the nanosized worm-like carbon, and 1744 m2 g-1 for the nitrogen-enriched microsized carbon. Both carbon materials demonstrate excellent energy storage capability as electrodes for aqueous supercapacitors. According to the three-electrode measurements, the worm-like carbon exhibits a high specific capacitance of 316 F g-1 at 0.2 A g-1 in 6 M KOH, while the other exhibits 471 F g-1 due to the highly enriched nitrogen atoms in structure. In addition, two-electrode coin-type cells have been assembled with the carbon materials as electrodes and hydrophilic poly(vinylidene fluoride) porous membrane as the separator. The assembled cells exhibit high specific capacitances, excellent rate performance and superior cycling durability because of a synergistic effect of the high performance carbon electrodes and hydrophilic porous separator.</p> </li> <li> <p><a target="_blank" rel="noopener noreferrer" onclick="trackOutboundLink('http://adsabs.harvard.edu/abs/2010JSSCh.183..969M','NASAADS'); return false;" href="http://adsabs.harvard.edu/abs/2010JSSCh.183..969M"><span>Carbon/ λ-MnO 2 composites for supercapacitor electrodes</span></a></p> <p><a target="_blank" rel="noopener noreferrer" href="http://adsabs.harvard.edu/abstract_service.html">NASA Astrophysics Data System (ADS)</a></p> <p>Malak-Polaczyk, A.; Matei-Ghimbeu, C.; Vix-Guterl, C.; Frackowiak, E.</p> <p>2010-04-01</p> <p>In the present work a composite of carbon with λ-MnO 2 have been synthesized by a simple two-step route. In the first step, to obtain LiMn 2O 4/carbon material, mesoporous activated carbon was impregnated with the solution of precursor metal salts and heated subsequently. As-prepared materials were acid treated which resulted in the formation of λ-MnO 2/carbon. Physical properties, structure and specific surface area of electrode materials were studied by TEM, X-ray diffraction and nitrogen sorption measurements. Voltammetry cycling, galvanostatic charge/discharge and impedance spectroscopy measurements performed in two- and three-electrode cells have been applied in order to measure electrochemical parameters. TEM images confirmed well dispersed λ-MnO 2 particles on the surface of carbon material. The carbon in the composite plays an important role as the surface area enhancing component and a support of pseudocapacitive material. Furthermore, the through-connected porosity serves as a continuous pathway for electrolyte transport. A synergetic effect of the porous carbon framework and of the redox properties of the λ-MnO 2 is at the origin of improvement of specific capacitance values which has been observed for composites after delithiation.</p> </li> <li> <p><a target="_blank" rel="noopener noreferrer" onclick="trackOutboundLink('https://www.gpo.gov/fdsys/pkg/CFR-2010-title40-vol12/pdf/CFR-2010-title40-vol12-part63-subpartUUUU-app6.pdf','CFR'); return false;" href="https://www.gpo.gov/fdsys/pkg/CFR-2010-title40-vol12/pdf/CFR-2010-title40-vol12-part63-subpartUUUU-app6.pdf"><span>40 CFR Table 6 to Subpart Uuuu of... - Continuous Compliance With Operating Limits</span></a></p> <p><a target="_blank" rel="noopener noreferrer" href="http://www.gpo.gov/fdsys/browse/collectionCfr.action?selectedYearFrom=2010&page.go=Go">Code of Federal Regulations, 2010 CFR</a></p> <p></p> <p>2010-07-01</p> <p>.... 7. carbon absorber maintain the regeneration frequency, total regeneration stream mass or volumetric flow during carbon bed regeneration and temperature of the carbon bed after regeneration (and within 15 minutes of completing any cooling cycle(s)) for each regeneration cycle within the values established...</p> </li> <li> <p><a target="_blank" rel="noopener noreferrer" onclick="trackOutboundLink('https://www.gpo.gov/fdsys/pkg/CFR-2011-title40-vol11/pdf/CFR-2011-title40-vol11-part63-subpartOOO-app4.pdf','CFR2011'); return false;" href="https://www.gpo.gov/fdsys/pkg/CFR-2011-title40-vol11/pdf/CFR-2011-title40-vol11-part63-subpartOOO-app4.pdf"><span>40 CFR Table 4 to Subpart Ooo of... - Operating Parameter Levels</span></a></p> <p><a target="_blank" rel="noopener noreferrer" href="http://www.gpo.gov/fdsys/browse/collectionCfr.action?selectedYearFrom=2011&page.go=Go">Code of Federal Regulations, 2011 CFR</a></p> <p></p> <p>2011-07-01</p> <p>... specific gravity Condenser Exit temperature Maximum temperature Carbon absorber Total regeneration steam or nitrogen flow, or pressure (gauge or absolute) a during carbon bed regeneration cycle; and temperature of the carbon bed after regeneration (and within 15 minutes of completing any cooling cycle(s)) Maximum...</p> </li> <li> <p><a target="_blank" rel="noopener noreferrer" onclick="trackOutboundLink('https://www.gpo.gov/fdsys/pkg/CFR-2013-title40-vol12/pdf/CFR-2013-title40-vol12-part63-subpartOOO-app4.pdf','CFR2013'); return false;" href="https://www.gpo.gov/fdsys/pkg/CFR-2013-title40-vol12/pdf/CFR-2013-title40-vol12-part63-subpartOOO-app4.pdf"><span>40 CFR Table 4 to Subpart Ooo of... - Operating Parameter Levels</span></a></p> <p><a target="_blank" rel="noopener noreferrer" href="http://www.gpo.gov/fdsys/browse/collectionCfr.action?selectedYearFrom=2013&page.go=Go">Code of Federal Regulations, 2013 CFR</a></p> <p></p> <p>2013-07-01</p> <p>... specific gravity Condenser Exit temperature Maximum temperature Carbon absorber Total regeneration steam or nitrogen flow, or pressure (gauge or absolute) a during carbon bed regeneration cycle; and temperature of the carbon bed after regeneration (and within 15 minutes of completing any cooling cycle(s)) Maximum...</p> </li> </ol> <div class="pull-right"> <ul class="pagination"> <li><a href="#" onclick='return showDiv("page_1");'>«</a></li> <li><a href="#" onclick='return showDiv("page_19");'>19</a></li> <li><a href="#" onclick='return showDiv("page_20");'>20</a></li> <li class="active"><span>21</span></li> <li><a href="#" onclick='return showDiv("page_22");'>22</a></li> <li><a href="#" onclick='return showDiv("page_23");'>23</a></li> <li><a href="#" onclick='return showDiv("page_25");'>»</a></li> </ul> </div> </div><!-- col-sm-12 --> </div><!-- row --> </div><!-- page_21 --> <div id="page_22" class="hiddenDiv"> <div class="row"> <div class="col-sm-12"> <div class="pull-right"> <ul class="pagination"> <li><a href="#" onclick='return showDiv("page_1");'>«</a></li> <li><a href="#" onclick='return showDiv("page_20");'>20</a></li> <li><a href="#" onclick='return showDiv("page_21");'>21</a></li> <li class="active"><span>22</span></li> <li><a href="#" onclick='return showDiv("page_23");'>23</a></li> <li><a href="#" onclick='return showDiv("page_24");'>24</a></li> <li><a href="#" onclick='return showDiv("page_25");'>»</a></li> </ul> </div> </div> </div> <div class="row"> <div class="col-sm-12"> <ol class="result-class" start="421"> <li> <p><a target="_blank" rel="noopener noreferrer" onclick="trackOutboundLink('https://www.gpo.gov/fdsys/pkg/CFR-2013-title40-vol13/pdf/CFR-2013-title40-vol13-part63-subpartUUUU-app6.pdf','CFR2013'); return false;" href="https://www.gpo.gov/fdsys/pkg/CFR-2013-title40-vol13/pdf/CFR-2013-title40-vol13-part63-subpartUUUU-app6.pdf"><span>40 CFR Table 6 to Subpart Uuuu of... - Continuous Compliance With Operating Limits</span></a></p> <p><a target="_blank" rel="noopener noreferrer" href="http://www.gpo.gov/fdsys/browse/collectionCfr.action?selectedYearFrom=2013&page.go=Go">Code of Federal Regulations, 2013 CFR</a></p> <p></p> <p>2013-07-01</p> <p>.... 7. carbon absorber maintain the regeneration frequency, total regeneration stream mass or volumetric flow during carbon bed regeneration and temperature of the carbon bed after regeneration (and within 15 minutes of completing any cooling cycle(s)) for each regeneration cycle within the values established...</p> </li> <li> <p><a target="_blank" rel="noopener noreferrer" onclick="trackOutboundLink('https://www.gpo.gov/fdsys/pkg/CFR-2014-title40-vol12/pdf/CFR-2014-title40-vol12-part63-subpartOOO-app4.pdf','CFR2014'); return false;" href="https://www.gpo.gov/fdsys/pkg/CFR-2014-title40-vol12/pdf/CFR-2014-title40-vol12-part63-subpartOOO-app4.pdf"><span>40 CFR Table 4 to Subpart Ooo of... - Operating Parameter Levels</span></a></p> <p><a target="_blank" rel="noopener noreferrer" href="http://www.gpo.gov/fdsys/browse/collectionCfr.action?selectedYearFrom=2014&page.go=Go">Code of Federal Regulations, 2014 CFR</a></p> <p></p> <p>2014-07-01</p> <p>... specific gravity Condenser Exit temperature Maximum temperature Carbon absorber Total regeneration steam or nitrogen flow, or pressure (gauge or absolute) a during carbon bed regeneration cycle; and temperature of the carbon bed after regeneration (and within 15 minutes of completing any cooling cycle(s)) Maximum...</p> </li> <li> <p><a target="_blank" rel="noopener noreferrer" onclick="trackOutboundLink('https://www.gpo.gov/fdsys/pkg/CFR-2011-title40-vol12/pdf/CFR-2011-title40-vol12-part63-subpartUUUU-app6.pdf','CFR2011'); return false;" href="https://www.gpo.gov/fdsys/pkg/CFR-2011-title40-vol12/pdf/CFR-2011-title40-vol12-part63-subpartUUUU-app6.pdf"><span>40 CFR Table 6 to Subpart Uuuu of... - Continuous Compliance With Operating Limits</span></a></p> <p><a target="_blank" rel="noopener noreferrer" href="http://www.gpo.gov/fdsys/browse/collectionCfr.action?selectedYearFrom=2011&page.go=Go">Code of Federal Regulations, 2011 CFR</a></p> <p></p> <p>2011-07-01</p> <p>.... 7. carbon absorber maintain the regeneration frequency, total regeneration stream mass or volumetric flow during carbon bed regeneration and temperature of the carbon bed after regeneration (and within 15 minutes of completing any cooling cycle(s)) for each regeneration cycle within the values established...</p> </li> <li> <p><a target="_blank" rel="noopener noreferrer" onclick="trackOutboundLink('https://www.gpo.gov/fdsys/pkg/CFR-2014-title40-vol13/pdf/CFR-2014-title40-vol13-part63-subpartUUUU-app6.pdf','CFR2014'); return false;" href="https://www.gpo.gov/fdsys/pkg/CFR-2014-title40-vol13/pdf/CFR-2014-title40-vol13-part63-subpartUUUU-app6.pdf"><span>40 CFR Table 6 to Subpart Uuuu of... - Continuous Compliance With Operating Limits</span></a></p> <p><a target="_blank" rel="noopener noreferrer" href="http://www.gpo.gov/fdsys/browse/collectionCfr.action?selectedYearFrom=2014&page.go=Go">Code of Federal Regulations, 2014 CFR</a></p> <p></p> <p>2014-07-01</p> <p>.... 7. carbon absorber maintain the regeneration frequency, total regeneration stream mass or volumetric flow during carbon bed regeneration and temperature of the carbon bed after regeneration (and within 15 minutes of completing any cooling cycle(s)) for each regeneration cycle within the values established...</p> </li> <li> <p><a target="_blank" rel="noopener noreferrer" onclick="trackOutboundLink('https://www.gpo.gov/fdsys/pkg/CFR-2012-title40-vol12/pdf/CFR-2012-title40-vol12-part63-subpartOOO-app4.pdf','CFR2012'); return false;" href="https://www.gpo.gov/fdsys/pkg/CFR-2012-title40-vol12/pdf/CFR-2012-title40-vol12-part63-subpartOOO-app4.pdf"><span>40 CFR Table 4 to Subpart Ooo of... - Operating Parameter Levels</span></a></p> <p><a target="_blank" rel="noopener noreferrer" href="http://www.gpo.gov/fdsys/browse/collectionCfr.action?selectedYearFrom=2012&page.go=Go">Code of Federal Regulations, 2012 CFR</a></p> <p></p> <p>2012-07-01</p> <p>... temperature Maximum temperature Carbon absorber Total regeneration steam or nitrogen flow, or pressure (gauge or absolute) a during carbon bed regeneration cycle; and temperature of the carbon bed after regeneration (and within 15 minutes of completing any cooling cycle(s)) Maximum flow or pressure; and maximum...</p> </li> <li> <p><a target="_blank" rel="noopener noreferrer" onclick="trackOutboundLink('https://www.gpo.gov/fdsys/pkg/CFR-2012-title40-vol13/pdf/CFR-2012-title40-vol13-part63-subpartUUUU-app6.pdf','CFR2012'); return false;" href="https://www.gpo.gov/fdsys/pkg/CFR-2012-title40-vol13/pdf/CFR-2012-title40-vol13-part63-subpartUUUU-app6.pdf"><span>40 CFR Table 6 to Subpart Uuuu of... - Continuous Compliance With Operating Limits</span></a></p> <p><a target="_blank" rel="noopener noreferrer" href="http://www.gpo.gov/fdsys/browse/collectionCfr.action?selectedYearFrom=2012&page.go=Go">Code of Federal Regulations, 2012 CFR</a></p> <p></p> <p>2012-07-01</p> <p>.... 7. carbon absorber maintain the regeneration frequency, total regeneration stream mass or volumetric flow during carbon bed regeneration and temperature of the carbon bed after regeneration (and within 15 minutes of completing any cooling cycle(s)) for each regeneration cycle within the values established...</p> </li> <li> <p><a target="_blank" rel="noopener noreferrer" onclick="trackOutboundLink('http://hdl.handle.net/2060/19940026117','NASA-TRS'); return false;" href="http://hdl.handle.net/2060/19940026117"><span>The carbon cycle revisited</span></a></p> <p><a target="_blank" rel="noopener noreferrer" href="http://ntrs.nasa.gov/search.jsp">NASA Technical Reports Server (NTRS)</a></p> <p>Bolin, Bert; Fung, Inez</p> <p>1992-01-01</p> <p>Discussions during the Global Change Institute indicated a need to present, in some detail and as accurately as possible, our present knowledge about the carbon cycle, the uncertainties in this knowledge, and the reasons for these uncertainties. We discuss basic issues of internal consistency within the carbon cycle, and end by summarizing the key unknowns.</p> </li> <li> <p><a target="_blank" rel="noopener noreferrer" onclick="trackOutboundLink('https://cfpub.epa.gov/si/si_public_record_report.cfm?dirEntryId=252230&Lab=OAP&keyword=cycles&actType=&TIMSType=+&TIMSSubTypeID=&DEID=&epaNumber=&ntisID=&archiveStatus=Both&ombCat=Any&dateBeginCreated=&dateEndCreated=&dateBeginPublishedPresented=&dateEndPublishedPresented=&dateBeginUpdated=&dateEndUpdated=&dateBeginCompleted=&dateEndCompleted=&personID=&role=Any&journalID=&publisherID=&sortBy=revisionDate&count=50','EPA-EIMS'); return false;" href="https://cfpub.epa.gov/si/si_public_record_report.cfm?dirEntryId=252230&Lab=OAP&keyword=cycles&actType=&TIMSType=+&TIMSSubTypeID=&DEID=&epaNumber=&ntisID=&archiveStatus=Both&ombCat=Any&dateBeginCreated=&dateEndCreated=&dateBeginPublishedPresented=&dateEndPublishedPresented=&dateBeginUpdated=&dateEndUpdated=&dateBeginCompleted=&dateEndCompleted=&personID=&role=Any&journalID=&publisherID=&sortBy=revisionDate&count=50"><span>The effects of climate sensitivity and carbon cycle interactions on mitigation policy stringency</span></a></p> <p><a target="_blank" rel="noopener noreferrer" href="http://oaspub.epa.gov/eims/query.page">EPA Science Inventory</a></p> <p></p> <p></p> <p>Climate sensitivity and climate-carbon cycle feedbacks interact to determine how global carbon and energy cycles will change in the future. While the science of these connections is well documented, their economic implications are not well understood. Here we examine the effect o...</p> </li> <li> <p><a target="_blank" rel="noopener noreferrer" onclick="trackOutboundLink('https://www.osti.gov/pages/biblio/1406756-diurnal-cycling-rhizosphere-bacterial-communities-associated-shifts-carbon-metabolism','SCIGOV-DOEP'); return false;" href="https://www.osti.gov/pages/biblio/1406756-diurnal-cycling-rhizosphere-bacterial-communities-associated-shifts-carbon-metabolism"><span>Diurnal cycling of rhizosphere bacterial communities is associated with shifts in carbon metabolism</span></a></p> <p><a target="_blank" rel="noopener noreferrer" href="http://www.osti.gov/pages">DOE PAGES</a></p> <p>Staley, Christopher; Ferrieri, Abigail P.; Tfaily, Malak M.; ...</p> <p>2017-06-24</p> <p>The circadian clock regulates plant metabolic functions and is an important component in plant health and productivity. Rhizosphere bacteria play critical roles in plant growth, health, and development and are shaped primarily by soil communities. Using Illumina next-generation sequencing and high-resolution mass spectrometry, we characterized bacterial communities of wild-type (Col-0) Arabidopsis thaliana and an acyclic line (OX34) ectopically expressing the circadian clock-associated cca1 transcription factor, relative to a soil control, to determine how cycling dynamics affected the microbial community. Microbial communities associated with Brachypodium distachyon (BD21) were also evaluated.Significantly different bacterial community structures ( P = 0.031) were observed inmore » the rhizosphere of wild-type plants between light and dark cycle samples. Furthermore, 13% of the community showed cycling, with abundances of several families, including Burkholderiaceae, Rhodospirillaceae, Planctomycetaceae, and Gaiellaceae, exhibiting fluctuation in abundances relative to the light cycle. However, limited-to-no cycling was observed in the acyclic CCAox34 line or in soil controls. Significant cycling was also observed, to a lesser extent, in Brachypodium. Functional gene inference revealed that genes involved in carbohydrate metabolism were likely more abundant in near-dawn, dark samples. Additionally, the composition of organic matter in the rhizosphere showed a significant variation between dark and light cycles.The results of this study suggest that the rhizosphere bacterial community is regulated, to some extent, by the circadian clock and is likely influenced by, and exerts influences, on plant metabolism and productivity. The timing of bacterial cycling in relation to that of Arabidopsis further suggests that diurnal dynamics influence plant-microbe carbon metabolism and exchange. Equally important, our results suggest that previous studies done without relevance to time of day may need to be reevaluated with regard to the impact of diurnal cycles on the rhizosphere microbial community.« less</p> </li> <li> <p><a target="_blank" rel="noopener noreferrer" onclick="trackOutboundLink('https://www.osti.gov/servlets/purl/1406756','SCIGOV-STC'); return false;" href="https://www.osti.gov/servlets/purl/1406756"><span>Diurnal cycling of rhizosphere bacterial communities is associated with shifts in carbon metabolism</span></a></p> <p><a target="_blank" rel="noopener noreferrer" href="http://www.osti.gov/search">DOE Office of Scientific and Technical Information (OSTI.GOV)</a></p> <p>Staley, Christopher; Ferrieri, Abigail P.; Tfaily, Malak M.</p> <p></p> <p>The circadian clock regulates plant metabolic functions and is an important component in plant health and productivity. Rhizosphere bacteria play critical roles in plant growth, health, and development and are shaped primarily by soil communities. Using Illumina next-generation sequencing and high-resolution mass spectrometry, we characterized bacterial communities of wild-type (Col-0) Arabidopsis thaliana and an acyclic line (OX34) ectopically expressing the circadian clock-associated cca1 transcription factor, relative to a soil control, to determine how cycling dynamics affected the microbial community. Microbial communities associated with Brachypodium distachyon (BD21) were also evaluated.Significantly different bacterial community structures ( P = 0.031) were observed inmore » the rhizosphere of wild-type plants between light and dark cycle samples. Furthermore, 13% of the community showed cycling, with abundances of several families, including Burkholderiaceae, Rhodospirillaceae, Planctomycetaceae, and Gaiellaceae, exhibiting fluctuation in abundances relative to the light cycle. However, limited-to-no cycling was observed in the acyclic CCAox34 line or in soil controls. Significant cycling was also observed, to a lesser extent, in Brachypodium. Functional gene inference revealed that genes involved in carbohydrate metabolism were likely more abundant in near-dawn, dark samples. Additionally, the composition of organic matter in the rhizosphere showed a significant variation between dark and light cycles.The results of this study suggest that the rhizosphere bacterial community is regulated, to some extent, by the circadian clock and is likely influenced by, and exerts influences, on plant metabolism and productivity. The timing of bacterial cycling in relation to that of Arabidopsis further suggests that diurnal dynamics influence plant-microbe carbon metabolism and exchange. Equally important, our results suggest that previous studies done without relevance to time of day may need to be reevaluated with regard to the impact of diurnal cycles on the rhizosphere microbial community.« less</p> </li> <li> <p><a target="_blank" rel="noopener noreferrer" onclick="trackOutboundLink('http://adsabs.harvard.edu/abs/2017AGUFM.H43F1709L','NASAADS'); return false;" href="http://adsabs.harvard.edu/abs/2017AGUFM.H43F1709L"><span>Three-Dimensional Water and Carbon Cycle Modeling at High Spatial-Temporal Resolutions</span></a></p> <p><a target="_blank" rel="noopener noreferrer" href="http://adsabs.harvard.edu/abstract_service.html">NASA Astrophysics Data System (ADS)</a></p> <p>Liao, C.; Zhuang, Q.</p> <p>2017-12-01</p> <p>Terrestrial ecosystems in cryosphere are very sensitive to the global climate change due to the presence of snow covers, mountain glaciers and permafrost, especially when the increase in near surface air temperature is almost twice as large as the global average. However, few studies have investigated the water and carbon cycle dynamics using process-based hydrological and biogeochemistry modeling approach. In this study, we used three-dimensional modeling approach at high spatial-temporal resolutions to investigate the water and carbon cycle dynamics for the Tanana Flats Basin in interior Alaska with emphases on dissolved organic carbon (DOC) dynamics. The results have shown that: (1) lateral flow plays an important role in water and carbon cycle, especially in dissolved organic carbon (DOC) dynamics. (2) approximately 2.0 × 104 kg C yr-1 DOC is exported to the hydrological networks and it compromises 1% and 0.01% of total annual gross primary production (GPP) and total organic carbon stored in soil, respectively. This study has established an operational and flexible framework to investigate and predict the water and carbon cycle dynamics under the changing climate.</p> </li> <li> <p><a target="_blank" rel="noopener noreferrer" onclick="trackOutboundLink('http://www.osti.gov/sciencecinema/biblio/1015160','SCIGOVIMAGE-SCICINEMA'); return false;" href="http://www.osti.gov/sciencecinema/biblio/1015160"><span>Global Impacts (Carbon Cycle 2.0)</span></a></p> <p><a target="_blank" rel="noopener noreferrer" href="http://www.osti.gov/sciencecinema/">ScienceCinema</a></p> <p>Gadgil, Ashok</p> <p>2018-05-04</p> <p>Ashok Gadgil, Faculty Senior Scientist and Acting Director, EETD, also Professor of Environmental Engineering, UC Berkeley, speaks at the Carbon Cycle 2.0 kick-off symposium Feb. 2, 2010. We emit more carbon into the atmosphere than natural processes are able to remove - an imbalance with negative consequences. Carbon Cycle 2.0 is a Berkeley Lab initiative to provide the science needed to restore this balance by integrating the Labs diverse research activities and delivering creative solutions toward a carbon-neutral energy future.</p> </li> <li> <p><a target="_blank" rel="noopener noreferrer" onclick="trackOutboundLink('http://adsabs.harvard.edu/abs/2014JPS...254...18W','NASAADS'); return false;" href="http://adsabs.harvard.edu/abs/2014JPS...254...18W"><span>Self-assembled mesoporous TiO2/carbon nanotube composite with a three-dimensional conducting nanonetwork as a high-rate anode material for lithium-ion battery</span></a></p> <p><a target="_blank" rel="noopener noreferrer" href="http://adsabs.harvard.edu/abstract_service.html">NASA Astrophysics Data System (ADS)</a></p> <p>Wang, Jie; Ran, Ran; Tade, Moses O.; Shao, Zongping</p> <p>2014-05-01</p> <p>Mesoporous three-dimensional (3D) TiO2/carbon nanotube conductive hybrid nanostructures can be successfully developed using polyethylene oxide (PEO) to modify the surfaces of carbon nanotubes (CNTs). During the synthesis process, PEO acts as not only "bridges" to connect the TiO2 nanoparticles to the CNT surfaces but also as "hosts" to accommodate and stabilize the in situ generated TiO2 particles. As the electrodes for lithium-ion batteries, such mesoporous 3D TiO2/CNT hybrids, demonstrate high Li storage capacity, superior rate performance and excellent long-term cycling stability. They exhibit a reversible specific capacity of 203 mA h g-1 at 100 mA g-1 and a stable capacity retention of 91 mA h g-1 at 8000 mA g-1 (47.6 C) over 100 cycles; they also retain approximately 90% (71 mA h g-1) of their initial discharge capacity after 900 cycles at an extremely high rate of 15,000 mA g-1 (89 C). This facile synthetic strategy to construct mesoporous 3D TiO2/CNT conductive hybrids provides a convenient route that efficiently assembles various inorganic oxide components on the CNTs' surfaces and enables the formation of heterogeneous nanostructures with novel functionalities. In particular, utilizing a conductive 3D CNT network can serve as a promising strategy for developing high-performance electrodes for Li secondary batteries and supercapacitors.</p> </li> <li> <p><a target="_blank" rel="noopener noreferrer" onclick="trackOutboundLink('https://www.osti.gov/biblio/5579787-cyclicity-silurian-island-arc-carbonates-alexander-terrane-alaska','SCIGOV-STC'); return false;" href="https://www.osti.gov/biblio/5579787-cyclicity-silurian-island-arc-carbonates-alexander-terrane-alaska"><span>Cyclicity in Silurian island-arc carbonates, Alexander terrane, Alaska</span></a></p> <p><a target="_blank" rel="noopener noreferrer" href="http://www.osti.gov/search">DOE Office of Scientific and Technical Information (OSTI.GOV)</a></p> <p>Kittredge, L.E.; Soja, C.M.</p> <p>1993-03-01</p> <p>Silurian carbonates from Alaska (Alexander terrane) record the evolution of a submarine platform during waning volcanism in an island arc. A detailed stratigraphic analysis of a 47 meter-thick sequence revealed the existence of cyclically repeated limestones: coral-stromatoporoid wackestones alternate with oncoid packstones and bioturbated, silty lime mudstones. The coral-stromatoporoid deposits are characterized by a low-diversity assemblage of dendroid corals, massive stromatoporoids, Atrypoidea brachiopods, and rare occurrences of biostromes associated with Solenopora, high-spired gastropods, and crinoids. Oncoids typically are 2-6 mm in diameter and form massive, meter-thick units. Coated grains are symmetrically developed, have a shell or algal nucleus, and aremore » also a minor component of coral-stromatoporoid beds. These lithologic units form seven, shallowing-upwards cycles (parasequences) that range in thickness from 3-9 meters. Coral-stomatoporoid wackestones form the base of each cycle and grade upwards into oncoid packstones with silty, lime mudstones at the top. This succession of lithofacies within each cycle reflects an increase in energy levels from relatively deeper water environments to relatively shallower ones. The lack of abrasion in the corals and stromatoporoids suggests predominantly quiet-water conditions in shallow subtidal areas affected by periodic turbulence. Comparison with correlative sections in Alaska and lack of correspondence with global sea level curves suggest that the primary cause of cyclicity was tectonic perturbations with secondary eustatic effects. Cyclic deposition in peri/subtidal sites was terminated by rapid drowning of the carbonate platform during late Silurian orogenesis.« less</p> </li> <li> <p><a target="_blank" rel="noopener noreferrer" onclick="trackOutboundLink('https://pubs.er.usgs.gov/publication/70118254','USGSPUBS'); return false;" href="https://pubs.er.usgs.gov/publication/70118254"><span>Empirical estimates to reduce modeling uncertainties of soil organic carbon in permafrost regions: a review of recent progress and remaining challenges</span></a></p> <p><a target="_blank" rel="noopener noreferrer" href="http://pubs.er.usgs.gov/pubs/index.jsp?view=adv">USGS Publications Warehouse</a></p> <p>Mishra, U.; Jastrow, J.D.; Matamala, R.; Hugelius, G.; Koven, C.D.; Harden, Jennifer W.; Ping, S.L.; Michaelson, G.J.; Fan, Z.; Miller, R.M.; McGuire, A.D.; Tarnocai, C.; Kuhry, P.; Riley, W.J.; Schaefer, K.; Schuur, E.A.G.; Jorgenson, M.T.; Hinzman, L.D.</p> <p>2013-01-01</p> <p>The vast amount of organic carbon (OC) stored in soils of the northern circumpolar permafrost region is a potentially vulnerable component of the global carbon cycle. However, estimates of the quantity, decomposability, and combustibility of OC contained in permafrost-region soils remain highly uncertain, thereby limiting our ability to predict the release of greenhouse gases due to permafrost thawing. Substantial differences exist between empirical and modeling estimates of the quantity and distribution of permafrost-region soil OC, which contribute to large uncertainties in predictions of carbon–climate feedbacks under future warming. Here, we identify research challenges that constrain current assessments of the distribution and potential decomposability of soil OC stocks in the northern permafrost region and suggest priorities for future empirical and modeling studies to address these challenges.</p> </li> <li> <p><a target="_blank" rel="noopener noreferrer" onclick="trackOutboundLink('http://adsabs.harvard.edu/abs/2018JPS...392...15H','NASAADS'); return false;" href="http://adsabs.harvard.edu/abs/2018JPS...392...15H"><span>α-MnO2 nanorods supported on porous graphitic carbon nitride as efficient electrocatalysts for lithium-air batteries</span></a></p> <p><a target="_blank" rel="noopener noreferrer" href="http://adsabs.harvard.edu/abstract_service.html">NASA Astrophysics Data System (ADS)</a></p> <p>Hang, Yang; Zhang, Chaofeng; Luo, Xiaoman; Xie, Yingshen; Xin, Sen; Li, Yutao; Zhang, Dawei; Goodenough, John B.</p> <p>2018-07-01</p> <p>Synthesis of α-MnO2 nanorods grown on porous graphitic carbon nitride (g-C3N4) sheets via a facile hydrothermal treatment gives a porous composite exhibiting higher activity for an air cathode than the individual component of α-MnO2 or porous g-C3N4 for both the oxygen reduction reaction (ORR) and oxygen evolution reaction (OER). The porous g-C3N4/α-MnO2 composite also exhibits better performance in a Li-air battery than pure α-MnO2 or XC-72 carbon catalysts, which includes superior discharge capacity, low voltage gap and high cycle stability. The α-MnO2 nanorods catalyze the OER and the porous g-C3N4 sheets catalyze the ORR.</p> </li> <li> <p><a target="_blank" rel="noopener noreferrer" onclick="trackOutboundLink('http://adsabs.harvard.edu/abs/2014AGUFM.B31B0020H','NASAADS'); return false;" href="http://adsabs.harvard.edu/abs/2014AGUFM.B31B0020H"><span>Genome-to-Watershed Predictive Understanding of Terrestrial Environments</span></a></p> <p><a target="_blank" rel="noopener noreferrer" href="http://adsabs.harvard.edu/abstract_service.html">NASA Astrophysics Data System (ADS)</a></p> <p>Hubbard, S. S.; Agarwal, D.; Banfield, J. F.; Beller, H. R.; Brodie, E.; Long, P.; Nico, P. S.; Steefel, C. I.; Tokunaga, T. K.; Williams, K. H.</p> <p>2014-12-01</p> <p>Although terrestrial environments play a critical role in cycling water, greenhouse gasses, and other life-critical elements, the complexity of interactions among component microbes, plants, minerals, migrating fluids and dissolved constituents hinders predictive understanding of system behavior. The 'Sustainable Systems 2.0' project is developing genome-to-watershed scale predictive capabilities to quantify how the microbiome affects biogeochemical watershed functioning, how watershed-scale hydro-biogeochemical processes affect microbial functioning, and how these interactions co-evolve with climate and land-use changes. Development of such predictive capabilities is critical for guiding the optimal management of water resources, contaminant remediation, carbon stabilization, and agricultural sustainability - now and with global change. Initial investigations are focused on floodplains in the Colorado River Basin, and include iterative model development, experiments and observations with an early emphasis on subsurface aspects. Field experiments include local-scale experiments at Rifle CO to quantify spatiotemporal metabolic and geochemical responses to O2and nitrate amendments as well as floodplain-scale monitoring to quantify genomic and biogeochemical response to natural hydrological perturbations. Information obtained from such experiments are represented within GEWaSC, a Genome-Enabled Watershed Simulation Capability, which is being developed to allow mechanistic interrogation of how genomic information stored in a subsurface microbiome affects biogeochemical cycling. This presentation will describe the genome-to-watershed scale approach as well as early highlights associated with the project. Highlights include: first insights into the diversity of the subsurface microbiome and metabolic roles of organisms involved in subsurface nitrogen, sulfur and hydrogen and carbon cycling; the extreme variability of subsurface DOC and hydrological controls on carbon and nitrogen cycling; geophysical identification of floodplain hotspots that are useful for model parameterization; and GEWaSC demonstration of how incorporation of identified microbial metabolic processes improves prediction of the larger system biogeochemical behavior.</p> </li> <li> <p><a target="_blank" rel="noopener noreferrer" onclick="trackOutboundLink('https://pubs.er.usgs.gov/publication/70171519','USGSPUBS'); return false;" href="https://pubs.er.usgs.gov/publication/70171519"><span>Dissolved organic carbon export and internal cycling in small, headwater lakes</span></a></p> <p><a target="_blank" rel="noopener noreferrer" href="http://pubs.er.usgs.gov/pubs/index.jsp?view=adv">USGS Publications Warehouse</a></p> <p>Stets, Edward G.; Striegl, Robert G.; Aiken, George R.</p> <p>2010-01-01</p> <p>Carbon (C) cycling in freshwater lakes is intense but poorly integrated into our current understanding of overall C transport from the land to the oceans. We quantified dissolved organic carbon export (DOCX) and compared it with modeled gross DOC mineralization (DOCR) to determine whether hydrologic or within-lake processes dominated DOC cycling in a small headwaters watershed in Minnesota, USA. We also used DOC optical properties to gather information about DOC sources. We then compared our results to a data set of approximately 1500 lakes in the Eastern USA (Eastern Lake Survey, ELS, data set) to place our results in context of lakes more broadly. In the open-basin lakes in our watershed (n = 5), DOCX ranged from 60 to 183 g C m−2 lake area yr−1, whereas DOCR ranged from 15 to 21 g C m−2 lake area yr−1, emphasizing that lateral DOC fluxes dominated. DOCX calculated in our study watershed clustered near the 75th percentile of open-basin lakes in the ELS data set, suggesting that these results were not unusual. In contrast, DOCX in closed-basin lakes (n = 2) was approximately 5 g C m−2 lake area yr−1, whereas DOCR was 37 to 42 g C m−2 lake area yr−1, suggesting that internal C cycling dominated. In the ELS data set, median DOCX was 32 and 12 g C m−2 yr−1 in open-basin and closed-basin lakes, respectively. Although not as high as what was observed in our study watershed, DOCX is an important component of lake C flux more generally, particularly in open-basin lakes.</p> </li> <li> <p><a target="_blank" rel="noopener noreferrer" onclick="trackOutboundLink('https://www.ncbi.nlm.nih.gov/pubmed/23897802','PUBMED'); return false;" href="https://www.ncbi.nlm.nih.gov/pubmed/23897802"><span>Soil organic carbon dust emission: an omitted global source of atmospheric CO2.</span></a></p> <p><a target="_blank" rel="noopener noreferrer" href="https://www.ncbi.nlm.nih.gov/entrez/query.fcgi?DB=pubmed">PubMed</a></p> <p>Chappell, Adrian; Webb, Nicholas P; Butler, Harry J; Strong, Craig L; McTainsh, Grant H; Leys, John F; Viscarra Rossel, Raphael A</p> <p>2013-10-01</p> <p>Soil erosion redistributes soil organic carbon (SOC) within terrestrial ecosystems, to the atmosphere and oceans. Dust export is an essential component of the carbon (C) and carbon dioxide (CO(2)) budget because wind erosion contributes to the C cycle by removing selectively SOC from vast areas and transporting C dust quickly offshore; augmenting the net loss of C from terrestrial systems. However, the contribution of wind erosion to rates of C release and sequestration is poorly understood. Here, we describe how SOC dust emission is omitted from national C accounting, is an underestimated source of CO(2) and may accelerate SOC decomposition. Similarly, long dust residence times in the unshielded atmospheric environment may considerably increase CO(2) emission. We developed a first approximation to SOC enrichment for a well-established dust emission model and quantified SOC dust emission for Australia (5.83 Tg CO(2)-e yr(-1)) and Australian agricultural soils (0.4 Tg CO(2)-e yr(-1)). These amount to underestimates for CO(2) emissions of ≈10% from combined C pools in Australia (year = 2000), ≈5% from Australian Rangelands and ≈3% of Australian Agricultural Soils by Kyoto Accounting. Northern hemisphere countries with greater dust emission than Australia are also likely to have much larger SOC dust emission. Therefore, omission of SOC dust emission likely represents a considerable underestimate from those nations' C accounts. We suggest that the omission of SOC dust emission from C cycling and C accounting is a significant global source of uncertainty. Tracing the fate of wind-eroded SOC in the dust cycle is therefore essential to quantify the release of CO(2) from SOC dust to the atmosphere and the contribution of SOC deposition to downwind C sinks. © 2013 John Wiley & Sons Ltd.</p> </li> <li> <p><a target="_blank" rel="noopener noreferrer" onclick="trackOutboundLink('http://adsabs.harvard.edu/abs/2017AGUFM.B23D2096H','NASAADS'); return false;" href="http://adsabs.harvard.edu/abs/2017AGUFM.B23D2096H"><span>Identifying the role of plant-microbial interactions in driving Arctic carbon cycle changes using a 13C isotope tracer</span></a></p> <p><a target="_blank" rel="noopener noreferrer" href="http://adsabs.harvard.edu/abstract_service.html">NASA Astrophysics Data System (ADS)</a></p> <p>Hough, M.; Tfaily, M. M.; Blazewicz, S.; Dorrepaal, E.; Crill, P. M.; Rich, V. I.; Saleska, S. R.</p> <p>2017-12-01</p> <p>Thawing arctic permafrost (which contains 30-50% of global soil carbon) is expected to drive substantial alterations to carbon (C) cycling that will accelerate climate change. As permafrost thaws, old C may decompose more rapidly and be released as methane (CH4) and carbon dioxide (CO2), but thawing soil can also increase plant productivity as perennial shrub communities transition to faster growing annual wetland plants. The effect of plant community changes on the C cycle is not yet well understood. It could mitigate C loss if C input rates are high enough, or it could increase contributions to CH4 emission (a more potent greenhouse gas than CO2) if it decomposes anaerobically. To investigate the influence of fresh plant litter inputs on peat organic material, microbial communities, and greenhouse gas emissions we traced 13C-enriched plant material from Eriophorum and Sphagnum plants added to arctic peat decomposition incubations into each of these components. High resolution FT-ICR mass spectrometry showed changes in the types of enriched compounds over time indicative of microbial processing. Density fractionation of microbial DNA showed enrichment of the microbial community indicating uptake of 13C-enriched compounds from the plant litter. CO2 and CH4 fluxes were highly 13C enriched and showed three distinct phases of flux after litter addition which were not seen in incubations with no litter added. Together, these lines of evidence indicate that fresh litter inputs may play an important role in structuring microbial decomposition. Future work will explore this influence through closer examination of organic matter and microbial community changes during decomposition.</p> </li> </ol> <div class="pull-right"> <ul class="pagination"> <li><a href="#" onclick='return showDiv("page_1");'>«</a></li> <li><a href="#" onclick='return showDiv("page_20");'>20</a></li> <li><a href="#" onclick='return showDiv("page_21");'>21</a></li> <li class="active"><span>22</span></li> <li><a href="#" onclick='return showDiv("page_23");'>23</a></li> <li><a href="#" onclick='return showDiv("page_24");'>24</a></li> <li><a href="#" onclick='return showDiv("page_25");'>»</a></li> </ul> </div> </div><!-- col-sm-12 --> </div><!-- row --> </div><!-- page_22 --> <div id="page_23" class="hiddenDiv"> <div class="row"> <div class="col-sm-12"> <div class="pull-right"> <ul class="pagination"> <li><a href="#" onclick='return showDiv("page_1");'>«</a></li> <li><a href="#" onclick='return showDiv("page_21");'>21</a></li> <li><a href="#" onclick='return showDiv("page_22");'>22</a></li> <li class="active"><span>23</span></li> <li><a href="#" onclick='return showDiv("page_24");'>24</a></li> <li><a href="#" onclick='return showDiv("page_25");'>25</a></li> <li><a href="#" onclick='return showDiv("page_25");'>»</a></li> </ul> </div> </div> </div> <div class="row"> <div class="col-sm-12"> <ol class="result-class" start="441"> <li> <p><a target="_blank" rel="noopener noreferrer" onclick="trackOutboundLink('http://adsabs.harvard.edu/abs/2017AGUFM.B43I..03F','NASAADS'); return false;" href="http://adsabs.harvard.edu/abs/2017AGUFM.B43I..03F"><span>Initializing carbon cycle predictions from the Community Land Model by assimilating global biomass observations</span></a></p> <p><a target="_blank" rel="noopener noreferrer" href="http://adsabs.harvard.edu/abstract_service.html">NASA Astrophysics Data System (ADS)</a></p> <p>Fox, A. M.; Hoar, T. J.; Smith, W. K.; Moore, D. J.</p> <p>2017-12-01</p> <p>The locations and longevity of terrestrial carbon sinks remain uncertain, however it is clear that in order to predict long-term climate changes the role of the biosphere in surface energy and carbon balance must be understood and incorporated into earth system models (ESMs). Aboveground biomass, the amount of carbon stored in vegetation, is a key component of the terrestrial carbon cycle, representing the balance of uptake through gross primary productivity (GPP), losses from respiration, senescence and mortality over hundreds of years. The best predictions of current and future land-atmosphere fluxes are likely from the integration of process-based knowledge contained in models and information from observations of changes in carbon stocks using data assimilation (DA). By exploiting long times series, it is possible to accurately detect variability and change in carbon cycle dynamics through monitoring ecosystem states, for example biomass derived from vegetation optical depth (VOD), and use this information to initialize models before making predictions. To make maximum use of information about the current state of global ecosystems when using models we have developed a system that combines the Community Land Model (CLM) with the Data Assimilation Research Testbed (DART), a community tool for ensemble DA. This DA system is highly innovative in its complexity, completeness and capabilities. Here we described a series of activities, using both Observation System Simulation Experiments (OSSEs) and real observations, that have allowed us to quantify the potential impact of assimilating VOD data into CLM-DART on future land-atmosphere fluxes. VOD data are particularly suitable to use in this activity due to their long temporal coverage and appropriate scale when combined with CLM, but their absolute values rely on many assumptions. Therefore, we have had to assess the implications of the VOD retrieval algorithms, with an emphasis on detecting uncertainty due to assumptions and inputs in the algorithms that are incompatible with those encoded within CLM. It is probable that VOD describes changes in biomass more accurately than absolute values, so in additional to sequential assimilation of observations, we have tested alternative filter algorithms, and assimilating VOD anomalies.</p> </li> <li> <p><a target="_blank" rel="noopener noreferrer" onclick="trackOutboundLink('http://adsabs.harvard.edu/abs/2009AGUFMGC13A0702C','NASAADS'); return false;" href="http://adsabs.harvard.edu/abs/2009AGUFMGC13A0702C"><span>21st Century Carbon-Climate Change as Simulated by the Canadian Earth System Model CanESM1</span></a></p> <p><a target="_blank" rel="noopener noreferrer" href="http://adsabs.harvard.edu/abstract_service.html">NASA Astrophysics Data System (ADS)</a></p> <p>Curry, C.; Christian, J. R.; Arora, V.; Boer, G. J.; Denman, K. L.; Flato, G. M.; Scinocca, J. F.; Merryfield, W. J.; Lee, W. G.; Yang, D.</p> <p>2009-12-01</p> <p>The Canadian Earth System Model CanESM1 is a fully coupled climate/carbon-cycle model with prognostic ocean and terrestrial components. The model has been used to simulate the 1850-2000 climate using historical greenhouse gas emissions, and future climates using IPCC emission scenarios. Modelled globally averaged CO2 concentration, land and ocean carbon uptake compare well with observation-based values at year 2000, as do the annual cycle and latitudinal distribution of CO2, instilling confidence that the model is suitable for future projections of carbon cycle behaviour in a changing climate. Land use change emissions are calculated explicitly using an observation-based time series of fractional coverage of different plant functional types. A more complete description of the model may be found in Arora et al. (2009). Differences in the land-atmosphere CO2 flux from the present to the future period under the SRES A2 emissions scenario show an increase in land sinks by a factor of 7.5 globally, mostly the result of CO2 fertilization. By contrast, the magnitude of the global ocean CO2 sink increases by a factor of only 2.3 by 2100. Expressed as a fraction of total emissions, ocean carbon uptake decreases throughout the 2000-2100 period, while land carbon uptake increases until around 2050, then declines. The result is an increase in airborne CO2 fraction after the mid-21st century, reaching a value of 0.55 by 2100. The simulated decline in ocean carbon uptake over the 21st century occurs despite steadily rising atmospheric CO2. This behaviour is usually attributed to climate-induced changes in surface temperature and salinity that reduce CO2 solubility, and increasing ocean stratification that weakens the biological pump. However, ocean biological processes such as dinitrogen fixation and calcification may also play an important role. Although not well understood at present, improved parameterizations of these processes will increase confidence in projections of future trends in CO2 uptake.</p> </li> <li> <p><a target="_blank" rel="noopener noreferrer" onclick="trackOutboundLink('http://adsabs.harvard.edu/abs/2013AGUFMGC43A1046F','NASAADS'); return false;" href="http://adsabs.harvard.edu/abs/2013AGUFMGC43A1046F"><span>One carbon cycle: Impacts of model integration, ecosystem process detail, model resolution, and initialization data, on projections of future climate mitigation strategies</span></a></p> <p><a target="_blank" rel="noopener noreferrer" href="http://adsabs.harvard.edu/abstract_service.html">NASA Astrophysics Data System (ADS)</a></p> <p>Fisk, J.; Hurtt, G. C.; le page, Y.; Patel, P. L.; Chini, L. P.; Sahajpal, R.; Dubayah, R.; Thomson, A. M.; Edmonds, J.; Janetos, A. C.</p> <p>2013-12-01</p> <p>Integrated assessment models (IAMs) simulate the interactions between human and natural systems at a global scale, representing a broad suite of phenomena across the global economy, energy system, land-use, and carbon cycling. Most proposed climate mitigation strategies rely on maintaining or enhancing the terrestrial carbon sink as a substantial contribution to restrain the concentration of greenhouse gases in the atmosphere, however most IAMs rely on simplified regional representations of terrestrial carbon dynamics. Our research aims to reduce uncertainties associated with forest modeling within integrated assessments, and to quantify the impacts of climate change on forest growth and productivity for integrated assessments of terrestrial carbon management. We developed the new Integrated Ecosystem Demography (iED) to increase terrestrial ecosystem process detail, resolution, and the utilization of remote sensing in integrated assessments. iED brings together state-of-the-art models of human society (GCAM), spatial land-use patterns (GLM) and terrestrial ecosystems (ED) in a fully coupled framework. The major innovative feature of iED is a consistent, process-based representation of ecosystem dynamics and carbon cycle throughout the human, terrestrial, land-use, and atmospheric components. One of the most challenging aspects of ecosystem modeling is to provide accurate initialization of land surface conditions to reflect non-equilibrium conditions, i.e., the actual successional state of the forest. As all plants in ED have an explicit height, it is one of the few ecosystem models that can be initialized directly with vegetation height data. Previous work has demonstrated that ecosystem model resolution and initialization data quality have a large effect on flux predictions at continental scales. Here we use a factorial modeling experiment to quantify the impacts of model integration, process detail, model resolution, and initialization data on projections of future climate mitigation strategies. We find substantial effects on key integrated assessment projections including the magnitude of emissions to mitigate, the economic value of ecosystem carbon storage, future land-use patterns, food prices and energy technology.</p> </li> <li> <p><a target="_blank" rel="noopener noreferrer" onclick="trackOutboundLink('https://www.ncbi.nlm.nih.gov/pubmed/24935751','PUBMED'); return false;" href="https://www.ncbi.nlm.nih.gov/pubmed/24935751"><span>Recycling of carbon dioxide to methanol and derived products - closing the loop.</span></a></p> <p><a target="_blank" rel="noopener noreferrer" href="https://www.ncbi.nlm.nih.gov/entrez/query.fcgi?DB=pubmed">PubMed</a></p> <p>Goeppert, Alain; Czaun, Miklos; Jones, John-Paul; Surya Prakash, G K; Olah, George A</p> <p>2014-12-07</p> <p>Starting with coal, followed by petroleum oil and natural gas, the utilization of fossil fuels has allowed the fast and unprecedented development of human society. However, the burning of these resources in ever increasing pace is accompanied by large amounts of anthropogenic CO2 emissions, which are outpacing the natural carbon cycle, causing adverse global environmental changes, the full extent of which is still unclear. Even through fossil fuels are still abundant, they are nevertheless limited and will, in time, be depleted. Chemical recycling of CO2 to renewable fuels and materials, primarily methanol, offers a powerful alternative to tackle both issues, that is, global climate change and fossil fuel depletion. The energy needed for the reduction of CO2 can come from any renewable energy source such as solar and wind. Methanol, the simplest C1 liquid product that can be easily obtained from any carbon source, including biomass and CO2, has been proposed as a key component of such an anthropogenic carbon cycle in the framework of a "Methanol Economy". Methanol itself is an excellent fuel for internal combustion engines, fuel cells, stoves, etc. It's dehydration product, dimethyl ether, is a diesel fuel and liquefied petroleum gas (LPG) substitute. Furthermore, methanol can be transformed to ethylene, propylene and most of the petrochemical products currently obtained from fossil fuels. The conversion of CO2 to methanol is discussed in detail in this review.</p> </li> <li> <p><a target="_blank" rel="noopener noreferrer" onclick="trackOutboundLink('https://www.osti.gov/biblio/1390910-insight-capacity-fading-mechanism-amorphous-se-confined-micro-mesoporous-carbon-matrix-ether-based-electrolytes','SCIGOV-STC'); return false;" href="https://www.osti.gov/biblio/1390910-insight-capacity-fading-mechanism-amorphous-se-confined-micro-mesoporous-carbon-matrix-ether-based-electrolytes"><span>Insight into the Capacity Fading Mechanism of Amorphous Se 2 S 5 Confined in Micro/Mesoporous Carbon Matrix in Ether-Based Electrolytes</span></a></p> <p><a target="_blank" rel="noopener noreferrer" href="http://www.osti.gov/search">DOE Office of Scientific and Technical Information (OSTI.GOV)</a></p> <p>Xu, Gui-Liang; Ma, Tianyuan; Sun, Cheng-Jun</p> <p>2016-04-13</p> <p>In contrast to the stable cycle performance of space confined Se-based cathodes for lithium batteries in carbonate-based electrolytes, their common capacity fading in ether-based electrolytes has been paid less attention and not yet well-addressed so far. In this work, the lithiation/delithiation of amorphous Se2S5 confined in micro/mesoporous carbon (Se2S5/MPC) cathode was investigated by in situ X-ray near edge absorption spectroscopy (XANES) and theoretical calculations. The Se2S5/MPC composite was synthesized by a modified vaporization-condensation method to ensure a good encapsulation of Se2S5 into the pores of MPC host. In situ XANES results illustrated that the lithiation/delithiation reversibility of Se component wasmore » gradually decreased in ether-based electrolytes, leading to an aggravated formation of long-chain polyselenides during cycling and further capacity decay. Moreover, ab initio calculations revealed that the binding energy of polyselenides (Li2Sen) with carbon host is in an order of Li2Se6 > Li2Se4 > Li2Se. The insights into the failure mechanism of Se-based cathode gain in this work are expected to serve as a guide for future design on high performance Se-based cathodes.« less</p> </li> <li> <p><a target="_blank" rel="noopener noreferrer" onclick="trackOutboundLink('https://www.ncbi.nlm.nih.gov/pubmed/21886160','PUBMED'); return false;" href="https://www.ncbi.nlm.nih.gov/pubmed/21886160"><span>Increased forest ecosystem carbon and nitrogen storage from nitrogen rich bedrock.</span></a></p> <p><a target="_blank" rel="noopener noreferrer" href="https://www.ncbi.nlm.nih.gov/entrez/query.fcgi?DB=pubmed">PubMed</a></p> <p>Morford, Scott L; Houlton, Benjamin Z; Dahlgren, Randy A</p> <p>2011-08-31</p> <p>Nitrogen (N) limits the productivity of many ecosystems worldwide, thereby restricting the ability of terrestrial ecosystems to offset the effects of rising atmospheric CO(2) emissions naturally. Understanding input pathways of bioavailable N is therefore paramount for predicting carbon (C) storage on land, particularly in temperate and boreal forests. Paradigms of nutrient cycling and limitation posit that new N enters terrestrial ecosystems solely from the atmosphere. Here we show that bedrock comprises a hitherto overlooked source of ecologically available N to forests. We report that the N content of soils and forest foliage on N-rich metasedimentary rocks (350-950 mg N kg(-1)) is elevated by more than 50% compared with similar temperate forest sites underlain by N-poor igneous parent material (30-70 mg N kg(-1)). Natural abundance N isotopes attribute this difference to rock-derived N: (15)N/(14)N values for rock, soils and plants are indistinguishable in sites underlain by N-rich lithology, in marked contrast to sites on N-poor substrates. Furthermore, forests associated with N-rich parent material contain on average 42% more carbon in above-ground tree biomass and 60% more carbon in the upper 30 cm of the soil than similar sites underlain by N-poor rocks. Our results raise the possibility that bedrock N input may represent an important and overlooked component of ecosystem N and C cycling elsewhere.</p> </li> <li> <p><a target="_blank" rel="noopener noreferrer" onclick="trackOutboundLink('http://adsabs.harvard.edu/abs/2017AGUFMPP34A..05G','NASAADS'); return false;" href="http://adsabs.harvard.edu/abs/2017AGUFMPP34A..05G"><span>Sulfur cycling in plays an important role in the development of Ocean Anoxic Events</span></a></p> <p><a target="_blank" rel="noopener noreferrer" href="http://adsabs.harvard.edu/abstract_service.html">NASA Astrophysics Data System (ADS)</a></p> <p>Gomes, M. L.; Raven, M. R.; Fike, D. A.; Gill, B. C.; Johnston, D. T.</p> <p>2017-12-01</p> <p>Ocean Anoxic Events (OAEs) are major carbon cycle perturbations marked by enhanced organic carbon deposition in the marine realm and carbon isotope excursions in organic and inorganic carbon. Although not as severe as the "big five" mass extinctions, OAEs had dire consequences for marine ecosystems and thus influenced Mesozoic evolutionary patterns. Sulfur cycle reconstructions provide insight into the biogeochemical processes that played a role in the development of OAEs because the sulfur cycle is linked with the carbon and oxygen cycles. We present sulfur and oxygen isotope records from carbonate-associated sulfate from the Toarcian OAE that documents a positive sulfate-oxygen isotope excursion of +6‰, which is similar to the magnitude of the positive sulfur isotope excursion documented at the same site and other globally distributed sites. This high-resolution record allows us to explore temporal variability in the onset of the isotopic excursions: the onset of the positive sulfate-oxygen isotope excursion occurs at the same stratigraphic interval as the onset of the positive carbon isotope excursion and both precede the onset of the positive sulfate-sulfur isotope excursion. Because oxygen is rapidly recycled during oxidative sulfur cycling, changes in oxidative sulfur cycling affect oxygen isotope values of sulfate without impacting sulfur isotope values. Thus, the early onset of the sulfate-oxygen isotope excursion implies a change in oxidative sulfur cycling, which is likely due to a shoaling of the zone of sulfate reduction. We explore the consequences of sulfate reduction zone shoaling for organic carbon preservation. Specifically, the sulfurization of organic matter, which makes organic matter less susceptible to degradation, occurs more rapidly when the top of the zone of sulfate reduction is near or above the sediment water interface. Therefore, we suggest that the shoaling of the sulfate reduction zone locally changed pathways of oxidative sulfur cycling and enhanced organic carbon preservation. Given synchronous changes in similar, globally-distributed depositional environments, this impacted the global biogeochemical cycles of oxygen, carbon, and nutrients in ways that sustained decreased oxygen availability and influenced extinction patterns of marine organisms.</p> </li> <li> <p><a target="_blank" rel="noopener noreferrer" onclick="trackOutboundLink('http://adsabs.harvard.edu/abs/2017AGUFMPA42A..17C','NASAADS'); return false;" href="http://adsabs.harvard.edu/abs/2017AGUFMPA42A..17C"><span>When Magma Meets Carbonate: Explosive Criminals of Climate Change?</span></a></p> <p><a target="_blank" rel="noopener noreferrer" href="http://adsabs.harvard.edu/abstract_service.html">NASA Astrophysics Data System (ADS)</a></p> <p>Carter, L. B.</p> <p>2017-12-01</p> <p>The natural carbon cycle is a key component of global climate change. Identifying and quantifying all processes in the cycle is essential to determine the effects of human greenhouse gas contributions and make future predictions. Volcanoes are the main natural source of carbon dioxide to the atmosphere [1]. In settings where carbonate rocks underlie the edifice, they can be consumed by magma passing through, which can release extra CO2, potentially explaining the extremely high emissions at Mount Etna in Italy [2-4]. We conduct laboratory experiments, mimicking conditions in the crust, to study how different carbonate rocks interact with hot magmas at pressure, and determine the amount of CO2 generated. We find that some types of magma can raise volcanic gas output and cause more explosive and dangerous eruptions [5-6]. Others are more likely to release hot fluids to the surrounding rocks, releasing CO2 by skarnification, which leaves economically important ores like in the western US [3,7] but can weaken the subsurface, potentially leading to landslides. Gas can also be released on the flanks of a volcano or in regions lacking an active volcano, due to the breakdown of certain carbonate rocks by heat [7], seen as bubbling springs in Yellowstone [8]. Our experiments indicate that if dolostone, not limestone, surrounds a magma chamber, over half the CO2 that was locked in the crust can escape even at lower temperatures a distance away. These processes are perhaps pertinent to why the Earth's climate was warm >50 million years ago, when more magma-carbonate interaction likely occurred than today [3] and thus contributed several times the current volcanic output [4] to the atmosphere. As significant parts of the long-term carbon cycle, it is necessary to include magma-carbonate reactions when considering climate changes before taking into account human input. [1] Aiuppa et al 2017 ESciRev (168) 24-47; [2] Ganino and Arndt 2009 Geol (37) 323-326; [3] Lee et al. 2013 Geosph (9) 21-36; [4] Burton et al. 2013 RiMG (75) 3232-254; [4] Chiodini et al. 2011 BullVolc (73) 531-542; [5] Carter and Dasgupta 2015 EPSL (427) 202-214; [6] Carter and Dasgupta 2016 G3 (17) 3893-3916; [7] Franzolin et al. 2011 CMP (161)213-227; [8] Werner and Brantley 2003 (4) 1061-1088.</p> </li> <li> <p><a target="_blank" rel="noopener noreferrer" onclick="trackOutboundLink('https://www.osti.gov/servlets/purl/865819','DOE-PATENT-XML'); return false;" href="https://www.osti.gov/servlets/purl/865819"><span>Cyclic process for producing methane in a tubular reactor with effective heat removal</span></a></p> <p><a target="_blank" rel="noopener noreferrer" href="http://www.osti.gov/doepatents">DOEpatents</a></p> <p>Frost, Albert C.; Yang, Chang-Lee</p> <p>1986-01-01</p> <p>Carbon monoxide-containing gas streams are converted to methane by a cyclic, essentially two-step process in which said carbon monoxide is disproportionated to form carbon dioxide and active surface carbon deposited on the surface of a catalyst, and said carbon is reacted with steam to form product methane and by-product carbon dioxide. The exothermic heat of reaction generated in each step is effectively removed during each complete cycle so as to avoid a build up of heat from cycle-to-cycle, with particularly advantageous techniques being employed for fixed bed, tubular and fluidized bed reactor operations.</p> </li> <li> <p><a target="_blank" rel="noopener noreferrer" onclick="trackOutboundLink('http://adsabs.harvard.edu/abs/2018EaFut...6..565R','NASAADS'); return false;" href="http://adsabs.harvard.edu/abs/2018EaFut...6..565R"><span>Integrated Assessment of Carbon Dioxide Removal</span></a></p> <p><a target="_blank" rel="noopener noreferrer" href="http://adsabs.harvard.edu/abstract_service.html">NASA Astrophysics Data System (ADS)</a></p> <p>Rickels, W.; Reith, F.; Keller, D.; Oschlies, A.; Quaas, M. F.</p> <p>2018-03-01</p> <p>To maintain the chance of keeping the average global temperature increase below 2°C and to limit long-term climate change, removing carbon dioxide from the atmosphere (carbon dioxide removal, CDR) is becoming increasingly necessary. We analyze optimal and cost-effective climate policies in the dynamic integrated assessment model (IAM) of climate and the economy (DICE2016R) and investigate (1) the utilization of (ocean) CDR under different climate objectives, (2) the sensitivity of policies with respect to carbon cycle feedbacks, and (3) how well carbon cycle feedbacks are captured in the carbon cycle models used in state-of-the-art IAMs. Overall, the carbon cycle model in DICE2016R shows clear improvements compared to its predecessor, DICE2013R, capturing much better long-term dynamics and also oceanic carbon outgassing due to excess oceanic storage of carbon from CDR. However, this comes at the cost of a (too) tight short-term remaining emission budget, limiting the model suitability to analyze low-emission scenarios accurately. With DICE2016R, the compliance with the 2°C goal is no longer feasible without negative emissions via CDR. Overall, the optimal amount of CDR has to take into account (1) the emission substitution effect and (2) compensation for carbon cycle feedbacks.</p> </li> <li> <p><a target="_blank" rel="noopener noreferrer" onclick="trackOutboundLink('http://adsabs.harvard.edu/abs/2017MCM....52..807K','NASAADS'); return false;" href="http://adsabs.harvard.edu/abs/2017MCM....52..807K"><span>Effect of Thermal Cycling on the Tensile Behavior of Polymer Composites Reinforced by Basalt and Carbon Fibers</span></a></p> <p><a target="_blank" rel="noopener noreferrer" href="http://adsabs.harvard.edu/abstract_service.html">NASA Astrophysics Data System (ADS)</a></p> <p>Khalili, S. Mohammad Reza; Najafi, Moslem; Eslami-Farsani, Reza</p> <p>2017-01-01</p> <p>The aim of the present work was to investigate the effect of thermal cycling on the tensile behavior of three types of polymer-matrix composites — a phenolic resin reinforced with woven basalt fibers, woven carbon fibers, and hybrid basalt and carbon fibers — in an ambient environment. For this purpose, tensile tests were performed on specimens previously subjected to a certain number of thermal cycles. The ultimate tensile strength of the specimen reinforced with woven basalt fibers had by 5% after thermal cycling, but the strength of the specimen with woven carbon fibers had reduced to a value by 11% higher than that before thermal cycling.</p> </li> <li> <p><a target="_blank" rel="noopener noreferrer" onclick="trackOutboundLink('https://eric.ed.gov/?q=algae&id=EJ758423','ERIC'); return false;" href="https://eric.ed.gov/?q=algae&id=EJ758423"><span>Seeing the Carbon Cycle</span></a></p> <p><a target="_blank" rel="noopener noreferrer" href="http://www.eric.ed.gov/ERICWebPortal/search/extended.jsp?_pageLabel=advanced">ERIC Educational Resources Information Center</a></p> <p>Drouin, Pamela; Welty, David J.; Repeta, Daniel; Engle-Belknap, Cheryl A.; Cramer, Catherine; Frashure, Kim; Chen, Robert</p> <p>2006-01-01</p> <p>In this article, the authors present a classroom experiment that was developed to introduce middle school learners to the carbon cycle. The experiment deals with transfer of CO[subscript 2] between liquid reservoirs and the effect CO[subscript 2] has on algae growth. It allows students to observe the influence of the carbon cycle on algae growth,…</p> </li> <li> <p><a target="_blank" rel="noopener noreferrer" onclick="trackOutboundLink('https://www.gpo.gov/fdsys/pkg/CFR-2011-title40-vol11/pdf/CFR-2011-title40-vol11-part63-subpartGGG-app4.pdf','CFR2011'); return false;" href="https://www.gpo.gov/fdsys/pkg/CFR-2011-title40-vol11/pdf/CFR-2011-title40-vol11-part63-subpartGGG-app4.pdf"><span>40 CFR Table 4 to Subpart Ggg of... - Monitoring Requirements for Control Devices a</span></a></p> <p><a target="_blank" rel="noopener noreferrer" href="http://www.gpo.gov/fdsys/browse/collectionCfr.action?selectedYearFrom=2011&page.go=Go">Code of Federal Regulations, 2011 CFR</a></p> <p></p> <p>2011-07-01</p> <p>... monitoring device, and 1. Total regeneration stream mass or volumetric flow during carbon bed regeneration cycle(s) 1. For each regeneration cycle, record the total regeneration stream mass or volumetric flow. Carbon bed temperature monitoring device 2. Temperature of carbon bed after regeneration 2. For each...</p> </li> <li> <p><a target="_blank" rel="noopener noreferrer" onclick="trackOutboundLink('https://www.gpo.gov/fdsys/pkg/CFR-2012-title40-vol12/pdf/CFR-2012-title40-vol12-part63-subpartGGG-app4.pdf','CFR2012'); return false;" href="https://www.gpo.gov/fdsys/pkg/CFR-2012-title40-vol12/pdf/CFR-2012-title40-vol12-part63-subpartGGG-app4.pdf"><span>40 CFR Table 4 to Subpart Ggg of... - Monitoring Requirements for Control Devices a</span></a></p> <p><a target="_blank" rel="noopener noreferrer" href="http://www.gpo.gov/fdsys/browse/collectionCfr.action?selectedYearFrom=2012&page.go=Go">Code of Federal Regulations, 2012 CFR</a></p> <p></p> <p>2012-07-01</p> <p>... monitoring device, and 1. Total regeneration stream mass or volumetric flow during carbon bed regeneration cycle(s) 1. For each regeneration cycle, record the total regeneration stream mass or volumetric flow. Carbon bed temperature monitoring device 2. Temperature of carbon bed after regeneration 2. For each...</p> </li> <li> <p><a target="_blank" rel="noopener noreferrer" onclick="trackOutboundLink('https://www.gpo.gov/fdsys/pkg/CFR-2010-title40-vol11/pdf/CFR-2010-title40-vol11-part63-subpartGGG-app4.pdf','CFR'); return false;" href="https://www.gpo.gov/fdsys/pkg/CFR-2010-title40-vol11/pdf/CFR-2010-title40-vol11-part63-subpartGGG-app4.pdf"><span>40 CFR Table 4 to Subpart Ggg of... - Monitoring Requirements for Control Devices a</span></a></p> <p><a target="_blank" rel="noopener noreferrer" href="http://www.gpo.gov/fdsys/browse/collectionCfr.action?selectedYearFrom=2010&page.go=Go">Code of Federal Regulations, 2010 CFR</a></p> <p></p> <p>2010-07-01</p> <p>... monitoring device, and 1. Total regeneration stream mass or volumetric flow during carbon bed regeneration cycle(s) 1. For each regeneration cycle, record the total regeneration stream mass or volumetric flow. Carbon bed temperature monitoring device 2. Temperature of carbon bed after regeneration 2. For each...</p> </li> <li> <p><a target="_blank" rel="noopener noreferrer" onclick="trackOutboundLink('https://www.gpo.gov/fdsys/pkg/CFR-2013-title40-vol12/pdf/CFR-2013-title40-vol12-part63-subpartOOO-app3.pdf','CFR2013'); return false;" href="https://www.gpo.gov/fdsys/pkg/CFR-2013-title40-vol12/pdf/CFR-2013-title40-vol12-part63-subpartOOO-app3.pdf"><span>40 CFR Table 3 to Subpart Ooo of... - Batch Process Vent Monitoring Requirements</span></a></p> <p><a target="_blank" rel="noopener noreferrer" href="http://www.gpo.gov/fdsys/browse/collectionCfr.action?selectedYearFrom=2013&page.go=Go">Code of Federal Regulations, 2013 CFR</a></p> <p></p> <p>2013-07-01</p> <p>...) temperature Continuous records as specified in § 63.1416(d). a Carbon adsorber a Total regeneration steam flow or nitrogen flow, or pressure (gauge or absolute) during carbon bed regeneration cycle(s), and Record the total regeneration steam flow or nitrogen flow, or pressure for each carbon bed regeneration cycle...</p> </li> <li> <p><a target="_blank" rel="noopener noreferrer" onclick="trackOutboundLink('https://www.gpo.gov/fdsys/pkg/CFR-2014-title40-vol12/pdf/CFR-2014-title40-vol12-part63-subpartOOO-app3.pdf','CFR2014'); return false;" href="https://www.gpo.gov/fdsys/pkg/CFR-2014-title40-vol12/pdf/CFR-2014-title40-vol12-part63-subpartOOO-app3.pdf"><span>40 CFR Table 3 to Subpart Ooo of... - Batch Process Vent Monitoring Requirements</span></a></p> <p><a target="_blank" rel="noopener noreferrer" href="http://www.gpo.gov/fdsys/browse/collectionCfr.action?selectedYearFrom=2014&page.go=Go">Code of Federal Regulations, 2014 CFR</a></p> <p></p> <p>2014-07-01</p> <p>...) temperature Continuous records as specified in § 63.1416(d). a Carbon adsorber a Total regeneration steam flow or nitrogen flow, or pressure (gauge or absolute) during carbon bed regeneration cycle(s), and Record the total regeneration steam flow or nitrogen flow, or pressure for each carbon bed regeneration cycle...</p> </li> <li> <p><a target="_blank" rel="noopener noreferrer" onclick="trackOutboundLink('https://www.osti.gov/biblio/7264152-possible-impacts-ozone-depletion-trophic-interactions-biogenic-vertical-carbon-flux-southern-ocean','SCIGOV-STC'); return false;" href="https://www.osti.gov/biblio/7264152-possible-impacts-ozone-depletion-trophic-interactions-biogenic-vertical-carbon-flux-southern-ocean"><span>Possible impacts of ozone depletion on trophic interactions and biogenic vertical carbon flux in the Southern Ocean</span></a></p> <p><a target="_blank" rel="noopener noreferrer" href="http://www.osti.gov/search">DOE Office of Scientific and Technical Information (OSTI.GOV)</a></p> <p>Marchant, H.J.; Davidson, A.</p> <p>1992-03-01</p> <p>Among the most productive region of the Southern Ocean is the marginal ice edge zone that trails the retreating ice edge in spring and early summer. The timing of this near-surface phytoplankton bloom coincides with seasonal stratospheric ozone depletion when UV irradiance is reportedly as high as in mid-summer. Recent investigations indicate that antarctic marine phytoplankton are presently UV stressed. The extent to which increasing UV radiation diminishes the ability of phytoplankton to fix C02 and/or leads to changes in their species composition is equivocal. The colonial stage in the life cycle of the alga Phaeocystis pouchetii is one ofmore » the major components of the bloom. The authors have found that this alga produces extracellular products which are strongly UV-B absorbing. When exposed to increasing levels of UV-B radiation, survival of antarctic colonial Phaeocystis was significantly greater than colonies of this species from temperate waters and of the single-celled stage of its life cycle which produces no UV-B-absorbing compounds. Phaeocystis is apparently a minor dietary component of Antarctic krill, Euphausia superba, and its nutritional value to crustacea is reportedly low. Phytoplankton, principally diatoms, together with fecal pellets and molted exoskeletons of grazers contribute most of the particulate carbon flux from the euphotic zone to deep water.« less</p> </li> <li> <p><a target="_blank" rel="noopener noreferrer" onclick="trackOutboundLink('http://adsabs.harvard.edu/abs/2017AGUFM.B22D..08J','NASAADS'); return false;" href="http://adsabs.harvard.edu/abs/2017AGUFM.B22D..08J"><span>Large-scale Patterns of 14C Age of Bulk Organic Carbon and Various Molecular Components in Grassland Soils</span></a></p> <p><a target="_blank" rel="noopener noreferrer" href="http://adsabs.harvard.edu/abstract_service.html">NASA Astrophysics Data System (ADS)</a></p> <p>Jia, J.; Liu, Z.; Cao, Z.; Chen, L.; He, J. S.; Haghipour, N.; Wacker, L.; Eglinton, T. I.; Feng, X.</p> <p>2017-12-01</p> <p>Unraveling the fate of organic carbon (OC) in soils is essential to understanding the impact of global changes on the global carbon cycle. Previous studies have shown that while various soil OC components have different decomposability, chemically labile OC can have old 14C ages. However, few studies have compared the 14C age of various soil OC components on a large scale, which may provide important information on the link between the age or turnover of soil OC components to their sources, molecular structures as well as environmental variables. In this project, a suite of soil profiles were sampled along a large-scale transect of temperate and alpine grasslands across the Tibetan and Mongolian Plateaus in China with contrasting climatic, vegetation and soil properties. Bulk OC and source-specific compounds (including fatty acids (FAs), diacids (DAs) and lignin phenols) were radiocarbon-dated to investigate the age and turnover dynamics of different OC pools and the mechanisms controlling their stability. Our results show that lignin phenols displayed a large 14C variability. Short-chain (C16, 18) FAs sourced from vascular plants as well as microorganisms were younger than plant-derived long-chain FAs and DAs, indicating that short-chain FAs were easier to be decomposed or newly synthesized. In the temperate grasslands, long-chain DAs were younger than FAs, while the opposite trend was observed in the alpine grasslands. Preliminary correlation analysis suggests that the age of short-chain FAs were mainly influenced by clay contents and climate, while reactive minerals, clay or silt particles were important factors in the stabilization of long-chain FAs, DAs and lignin phenols. Overall, our study provided a unique 14 C dataset of soil OC components in grasslands, which will provide important constraints on soil carbon turnover in future investigations.</p> </li> <li> <p><a target="_blank" rel="noopener noreferrer" onclick="trackOutboundLink('http://www.osti.gov/accomplishments/documents/fullText/ACC0249.pdf','DOE-RDACC'); return false;" href="http://www.osti.gov/accomplishments/documents/fullText/ACC0249.pdf"><span>Formulating Energy Policies Related to Fossil Fuel Use: Critical Uncertainties in the Global Carbon Cycle</span></a></p> <p><a target="_blank" rel="noopener noreferrer" href="http://www.osti.gov/accomplishments/fieldedsearch.html">DOE R&D Accomplishments Database</a></p> <p>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.</p> <p>1990-02-01</p> <p>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.</p> </li> </ol> <div class="pull-right"> <ul class="pagination"> <li><a href="#" onclick='return showDiv("page_1");'>«</a></li> <li><a href="#" onclick='return showDiv("page_21");'>21</a></li> <li><a href="#" onclick='return showDiv("page_22");'>22</a></li> <li class="active"><span>23</span></li> <li><a href="#" onclick='return showDiv("page_24");'>24</a></li> <li><a href="#" onclick='return showDiv("page_25");'>25</a></li> <li><a href="#" onclick='return showDiv("page_25");'>»</a></li> </ul> </div> </div><!-- col-sm-12 --> </div><!-- row --> </div><!-- page_23 --> <div id="page_24" class="hiddenDiv"> <div class="row"> <div class="col-sm-12"> <div class="pull-right"> <ul class="pagination"> <li><a href="#" onclick='return showDiv("page_1");'>«</a></li> <li><a href="#" onclick='return showDiv("page_21");'>21</a></li> <li><a href="#" onclick='return showDiv("page_22");'>22</a></li> <li><a href="#" onclick='return showDiv("page_23");'>23</a></li> <li class="active"><span>24</span></li> <li><a href="#" onclick='return showDiv("page_25");'>25</a></li> <li><a href="#" onclick='return showDiv("page_25");'>»</a></li> </ul> </div> </div> </div> <div class="row"> <div class="col-sm-12"> <ol class="result-class" start="461"> <li> <p><a target="_blank" rel="noopener noreferrer" onclick="trackOutboundLink('http://adsabs.harvard.edu/abs/2017AGUFM.B41G2052B','NASAADS'); return false;" href="http://adsabs.harvard.edu/abs/2017AGUFM.B41G2052B"><span>The Second State of the Carbon Cycle Report: A Scientific Basis for Policy and Management Decisions</span></a></p> <p><a target="_blank" rel="noopener noreferrer" href="http://adsabs.harvard.edu/abstract_service.html">NASA Astrophysics Data System (ADS)</a></p> <p>Birdsey, R.; Mayes, M. A.; Reed, S.; Najjar, R.; Romero-Lankao, P.</p> <p>2017-12-01</p> <p>The second "State of the Carbon Cycle of North America Report" (SOCCR-2) includes an overview of the North American carbon budget and future projections, the consequences of changes to the carbon budget, details of the carbon budget in major terrestrial and aquatic ecosystems (including coastal ocean waters), information about anthropogenic drivers, and implications for policy and carbon management. SOCCR-2 includes new focus areas such as soil carbon, arctic and boreal ecosystems, tribal lands, and greater emphasis on aquatic systems and the role of societal drivers and decision making on the carbon cycle. In addition, methane is considered to a greater extent than before. SOCCR-2 will contribute to the next U.S. National Climate Assessment, as well as providing information to support science-based management decisions and policies that include climate change mitigation and adaptation in Canada, the United States, and Mexico. Although the Report is still in the review process, preliminary findings indicate that North America is a net emitter of carbon dioxide and methane to the atmosphere, and that natural sinks offset about 25% of emitted carbon dioxide. Combustion of fossil fuels represents the largest source of emissions, but show a decreasing trend over the last decade and a lower share (20%) of the global total compared with the previous decade. Forests, soils, grasslands, and coastal oceans comprise the largest carbon sinks, while emissions from inland waters are a significant source of carbon dioxide. The Report also documents the lateral transfers of carbon among terrestrial ecosystems and from terrestrial to near-coastal ecosystems, to complete the carbon cycle accounting. Further, the Report explores the consequences of rising atmospheric carbon dioxide on terrestrial and oceanic systems, and the capacity of these systems to continue to act as carbon sinks based on the drivers of future carbon cycle changes, including carbon-climate feedbacks, atmospheric composition, nutrient availability, and human activity and management decisions. SOCCR-2 highlights key data gaps in carbon accounting frameworks, uncertainties in modeling and estimation approaches, and integrated frameworks for improving our understanding of the North American carbon cycle.</p> </li> <li> <p><a target="_blank" rel="noopener noreferrer" onclick="trackOutboundLink('http://adsabs.harvard.edu/abs/2017AGUFMGC14A..07H','NASAADS'); return false;" href="http://adsabs.harvard.edu/abs/2017AGUFMGC14A..07H"><span>Nonlinear Interactions between Climate and Atmospheric Carbon Dioxide Drivers of Terrestrial and Marine Carbon Cycle Changes</span></a></p> <p><a target="_blank" rel="noopener noreferrer" href="http://adsabs.harvard.edu/abstract_service.html">NASA Astrophysics Data System (ADS)</a></p> <p>Hoffman, F. M.; Randerson, J. T.; Moore, J. K.; Goulden, M.; Fu, W.; Koven, C.; Swann, A. L. S.; Mahowald, N. M.; Lindsay, K. T.; Munoz, E.</p> <p>2017-12-01</p> <p>Quantifying interactions between global biogeochemical cycles and the Earth system is important for predicting future atmospheric composition and informing energy policy. We applied a feedback analysis framework to three sets of Historical (1850-2005), Representative Concentration Pathway 8.5 (2006-2100), and its extension (2101-2300) simulations from the Community Earth System Model version 1.0 (CESM1(BGC)) to quantify drivers of terrestrial and ocean responses of carbon uptake. In the biogeochemically coupled simulation (BGC), the effects of CO2 fertilization and nitrogen deposition influenced marine and terrestrial carbon cycling. In the radiatively coupled simulation (RAD), the effects of rising temperature and circulation changes due to radiative forcing from CO2, other greenhouse gases, and aerosols were the sole drivers of carbon cycle changes. In the third, fully coupled simulation (FC), both the biogeochemical and radiative coupling effects acted simultaneously. We found that climate-carbon sensitivities derived from RAD simulations produced a net ocean carbon storage climate sensitivity that was weaker and a net land carbon storage climate sensitivity that was stronger than those diagnosed from the FC and BGC simulations. For the ocean, this nonlinearity was associated with warming-induced weakening of ocean circulation and mixing that limited exchange of dissolved inorganic carbon between surface and deeper water masses. For the land, this nonlinearity was associated with strong gains in gross primary production in the FC simulation, driven by enhancements in the hydrological cycle and increased nutrient availability. We developed and applied a nonlinearity metric to rank model responses and driver variables. The climate-carbon cycle feedback gain at 2300 was 42% higher when estimated from climate-carbon sensitivities derived from the difference between FC and BGC than when derived from RAD. We re-analyzed other CMIP5 model results to quantify the effects of such nonlinearities on their projected climate-carbon cycle feedback gains.</p> </li> <li> <p><a target="_blank" rel="noopener noreferrer" onclick="trackOutboundLink('https://www.fs.usda.gov/treesearch/pubs/55389','TREESEARCH'); return false;" href="https://www.fs.usda.gov/treesearch/pubs/55389"><span>Current systematic carbon-cycle observations and the need for implementing a policy-relevant carbon observing system</span></a></p> <p><a target="_blank" rel="noopener noreferrer" href="http://www.fs.usda.gov/treesearch/">Treesearch</a></p> <p>P. Ciais; A. J. Dolman; A. Bombelli; R. Duren; A. Peregon; P. J. Rayner; C. Miller; N. Gobron; G. Kinderman; G. Marland; N. Gruber; F. Chevallier; R. J. Andres; G. Balsamo; L. Bopp; F.-M. Bréon; G. Broquet; R. Dargaville; T. J. Battin; A. Borges; H. Bovensmann; M. Buchwitz; J. Butler; J. G. Canadell; R. B. Cook; R. DeFries; R. Engelen; K. R. Gurney; C. Heinze; M. Heimann; A. Held; M. Henry; B. Law; S. Luyssaert; J. Miller; T. Moriyama; C. Moulin; R. B. Myneni; C. Nussli; M. Obersteiner; D. Ojima; Y. Pan; J.-D. Paris; S. L. Piao; B. Poulter; S. Plummer; S. Quegan; P. Raymond; M. Reichstein; L. Rivier; C. Sabine; D. Schimel; O. Tarasova; R. Valentini; R. Wang; G. van der Werf; D. Wickland; M. Williams; C. Zehner</p> <p>2014-01-01</p> <p>A globally integrated carbon observation and analysis system is needed to improve the fundamental understanding of the global carbon cycle, to improve our ability to project future changes, and to verify the effectiveness of policies aiming to reduce greenhouse gas emissions and increase carbon sequestration. Building an integrated carbon observation system requires...</p> </li> <li> <p><a target="_blank" rel="noopener noreferrer" onclick="trackOutboundLink('http://www.osti.gov/sciencecinema/biblio/1015164','SCIGOVIMAGE-SCICINEMA'); return false;" href="http://www.osti.gov/sciencecinema/biblio/1015164"><span>Reducing Demand through Efficiency and Services: Impacts and Opportunities in Buildings Sector (Carbon Cycle 2.0)</span></a></p> <p><a target="_blank" rel="noopener noreferrer" href="http://www.osti.gov/sciencecinema/">ScienceCinema</a></p> <p>Piette, Mary Ann</p> <p>2018-05-03</p> <p>Mary Ann Piette, Deputy of LBNL's Building Technologies Department and Director of the Demand Response Research Center, speaks at the Carbon Cycle 2.0 kick-off symposium Feb. 2, 2010. We emit more carbon into the atmosphere than natural processes are able to remove - an imbalance with negative consequences. Carbon Cycle 2.0 is a Berkeley Lab initiative to provide the science needed to restore this balance by integrating the Labs diverse research activities and delivering creative solutions toward a carbon-neutral energy future.</p> </li> <li> <p><a target="_blank" rel="noopener noreferrer" onclick="trackOutboundLink('https://www.osti.gov/servlets/purl/1015164','SCIGOV-STC'); return false;" href="https://www.osti.gov/servlets/purl/1015164"><span>Reducing Demand through Efficiency and Services: Impacts and Opportunities in Buildings Sector (Carbon Cycle 2.0)</span></a></p> <p><a target="_blank" rel="noopener noreferrer" href="http://www.osti.gov/search">DOE Office of Scientific and Technical Information (OSTI.GOV)</a></p> <p>Piette, Mary Ann</p> <p></p> <p>Mary Ann Piette, Deputy of LBNL's Building Technologies Department and Director of the Demand Response Research Center, speaks at the Carbon Cycle 2.0 kick-off symposium Feb. 2, 2010. We emit more carbon into the atmosphere than natural processes are able to remove - an imbalance with negative consequences. Carbon Cycle 2.0 is a Berkeley Lab initiative to provide the science needed to restore this balance by integrating the Labs diverse research activities and delivering creative solutions toward a carbon-neutral energy future.</p> </li> <li> <p><a target="_blank" rel="noopener noreferrer" onclick="trackOutboundLink('http://adsabs.harvard.edu/abs/2013AGUFM.B12B..08L','NASAADS'); return false;" href="http://adsabs.harvard.edu/abs/2013AGUFM.B12B..08L"><span>Microbial processing of carbon in hydrothermal systems (Invited)</span></a></p> <p><a target="_blank" rel="noopener noreferrer" href="http://adsabs.harvard.edu/abstract_service.html">NASA Astrophysics Data System (ADS)</a></p> <p>LaRowe, D.; Amend, J. P.</p> <p>2013-12-01</p> <p>Microorganisms are known to be active in hydrothermal systems. They catalyze reactions that consume and produce carbon compounds as a result of their efforts to gain energy, grow and replace biomass. However, the rates of these processes, as well as the size of the active component of microbial populations, are poorly constrained in hydrothermal environments. In order to better characterize biogeochemical processes in these settings, a quantitative relationship between rates of microbial catalysis, energy supply and demand and population size is presented. Within this formulation, rates of biomass change are determined as a function of the proportion of catabolic power that is converted into biomass - either new microorganisms or the replacement of existing cell components - and the amount of energy that is required to synthesize biomass. The constraints that hydrothermal conditions place on power supply and demand are explicitly taken into account. The chemical composition, including the concentrations of organic compounds, of diffuse and focused flow hydrothermal fluids, hydrothermally influenced sediment pore water and fluids from the oceanic lithosphere are used in conjunction with cell count data and the model described above to constrain the rates of microbial processes that influence the carbon cycle in the Juan de Fuca hydrothermal system.</p> </li> <li> <p><a target="_blank" rel="noopener noreferrer" onclick="trackOutboundLink('https://www.ncbi.nlm.nih.gov/pubmed/26435332','PUBMED'); return false;" href="https://www.ncbi.nlm.nih.gov/pubmed/26435332"><span>Solar Thermochemical Energy Storage Through Carbonation Cycles of SrCO3/SrO Supported on SrZrO3.</span></a></p> <p><a target="_blank" rel="noopener noreferrer" href="https://www.ncbi.nlm.nih.gov/entrez/query.fcgi?DB=pubmed">PubMed</a></p> <p>Rhodes, Nathan R; Barde, Amey; Randhir, Kelvin; Li, Like; Hahn, David W; Mei, Renwei; Klausner, James F; AuYeung, Nick</p> <p>2015-11-01</p> <p>Solar thermochemical energy storage has enormous potential for enabling cost-effective concentrated solar power (CSP). A thermochemical storage system based on a SrO/SrCO3 carbonation cycle offers the ability to store and release high temperature (≈1200 °C) heat. The energy density of SrCO3/SrO systems supported by zirconia-based sintering inhibitors was investigated for 15 cycles of exothermic carbonation at 1150 °C followed by decomposition at 1235 °C. A sample with 40 wt % of SrO supported by yttria-stabilized zirconia (YSZ) shows good energy storage stability at 1450 MJ m(-3) over fifteen cycles at the same cycling temperatures. After further testing over 45 cycles, a decrease in energy storage capacity to 1260 MJ m(-3) is observed during the final cycle. The decrease is due to slowing carbonation kinetics, and the original value of energy density may be obtained by lengthening the carbonation steps. © 2015 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.</p> </li> <li> <p><a target="_blank" rel="noopener noreferrer" onclick="trackOutboundLink('http://adsabs.harvard.edu/abs/2003TrGeo...5..581R','NASAADS'); return false;" href="http://adsabs.harvard.edu/abs/2003TrGeo...5..581R"><span>Soils and Global Change in the Carbon Cycle over Geological Time</span></a></p> <p><a target="_blank" rel="noopener noreferrer" href="http://adsabs.harvard.edu/abstract_service.html">NASA Astrophysics Data System (ADS)</a></p> <p>Retallack, G. J.</p> <p>2003-12-01</p> <p>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 sedimentary rocks; organic matter burial is an important long-term control on CO2 levels in the atmosphere (Berner and Kothavala, 2001). The magnitudes of carbon pools and fluxes involved provide a perspective on the importance of soils compared with other carbon reservoirs ( Figure 1). (6K)Figure 1. Pools and fluxes of reduced carbon (bold) and oxidized carbon (regular) in Gt in the pre-industrial carbon cycle (sources Schidlowski and Aharon, 1992; Siegenthaler and Sarmiento, 1993; Stallard, 1998). Before industrialization, there was only 600 Gt (1 Gt=1015g) of carbon in CO2 and methane in the atmosphere, which is about the same amount as in all terrestrial biomass, but less than half of the reservoir of soil organic carbon. The ocean contained only ˜3 Gt of biomass carbon. The deep ocean and sediments comprised the largest reservoir of bicarbonate and organic matter, but that carbon has been kept out of circulation from the atmosphere for geologically significant periods of time (Schidlowski and Aharon, 1992). Humans have tapped underground reservoirs of fossil fuels, and our other perturbations of the carbon cycle have also been significant ( Vitousek et al., 1997b; see Chapter 8.10).Atmospheric increase of carbon in CO2 to 750 Gt C by deforestation and fossil fuel burning has driven ongoing global warming, but is not quite balanced by changes in the other carbon reservoirs leading to search for a "missing sink" of some 1.8±1.3 GtC, probably in terrestrial organisms, soils, and sediments of the northern hemisphere (Keeling et al., 1982; Siegenthaler and Sarmiento, 1993; Stallard, 1998). Soil organic matter is a big, rapidly cycling reservoir, likely to include much of this missing sink.During the geological past, the sizes of, and fluxes between, these reservoirs have varied enormously as the world has alternated between greenhouse times of high carbon content of the atmosphere, and icehouse times of low carbon content of the atmosphere. Oscillations in the atmospheric content of greenhouse gases can be measured, estimated, or modeled on all timescales from annual to eonal (Figure 2). The actively cycling surficial carbon reservoirs are biomass, surface oceans, air, and soils, so it is no surprise that the fossil record of life on Earth shows strong linkage to global climate change (Berner, 1997; Algeo and Scheckler, 1998; Retallack, 2000a). There is an additional line of evidence for past climatic and atmospheric history in the form of fossil soils, or paleosols, now known to be abundant throughout the geological record ( Retallack, 1997a, 2001a). This chapter addresses evidence from fossil soils for global climate change in the past, and attempts to assess the role of soils in carbon cycle fluctuations through the long history of our planet. (30K)Figure 2. Variation in atmospheric CO2 composition on a variety of timescales ranging from annual to eonal (a) Keeling et al., 1982; reproduced from Carban Dioxide Review 1982, 377-385 (b) Petit et al., 1999; reproduced by permission of Nature Publishing Group from Nature 1999, 399, 429-436 (c) Retallack, 2001d; reproduced by J. Geol. 2001, 109, 407-426 (d) Berner and Kothavala, 2001; reproduced by permission of American Journal of Science from Am. J. Sci. 2001, 301, 182-204.</p> </li> <li> <p><a target="_blank" rel="noopener noreferrer" onclick="trackOutboundLink('http://adsabs.harvard.edu/abs/2017NatEn...2..939P','NASAADS'); return false;" href="http://adsabs.harvard.edu/abs/2017NatEn...2..939P"><span>Understanding future emissions from low-carbon power systems by integration of life-cycle assessment and integrated energy modelling</span></a></p> <p><a target="_blank" rel="noopener noreferrer" href="http://adsabs.harvard.edu/abstract_service.html">NASA Astrophysics Data System (ADS)</a></p> <p>Pehl, Michaja; Arvesen, Anders; Humpenöder, Florian; Popp, Alexander; Hertwich, Edgar G.; Luderer, Gunnar</p> <p>2017-12-01</p> <p>Both fossil-fuel and non-fossil-fuel power technologies induce life-cycle greenhouse gas emissions, mainly due to their embodied energy requirements for construction and operation, and upstream CH4 emissions. Here, we integrate prospective life-cycle assessment with global integrated energy-economy-land-use-climate modelling to explore life-cycle emissions of future low-carbon power supply systems and implications for technology choice. Future per-unit life-cycle emissions differ substantially across technologies. For a climate protection scenario, we project life-cycle emissions from fossil fuel carbon capture and sequestration plants of 78-110 gCO2eq kWh-1, compared with 3.5-12 gCO2eq kWh-1 for nuclear, wind and solar power for 2050. Life-cycle emissions from hydropower and bioenergy are substantial (˜100 gCO2eq kWh-1), but highly uncertain. We find that cumulative emissions attributable to upscaling low-carbon power other than hydropower are small compared with direct sectoral fossil fuel emissions and the total carbon budget. Fully considering life-cycle greenhouse gas emissions has only modest effects on the scale and structure of power production in cost-optimal mitigation scenarios.</p> </li> <li> <p><a target="_blank" rel="noopener noreferrer" onclick="trackOutboundLink('http://adsabs.harvard.edu/abs/2011AGUFM.B31H0411Y','NASAADS'); return false;" href="http://adsabs.harvard.edu/abs/2011AGUFM.B31H0411Y"><span>Modeling carbon cycle process of soil profile in Loess Plateau of China</span></a></p> <p><a target="_blank" rel="noopener noreferrer" href="http://adsabs.harvard.edu/abstract_service.html">NASA Astrophysics Data System (ADS)</a></p> <p>Yu, Y.; Finke, P.; Guo, Z.; Wu, H.</p> <p>2011-12-01</p> <p>SoilGen2 is a process-based model, which could reconstruct soil formation under various climate conditions, parent materials, vegetation types, slopes, expositions and time scales. Both organic and inorganic carbon cycle processes could be simulated, while the later process is important in carbon cycle of arid and semi-arid regions but seldom being studied. After calibrating parameters of dust deposition rate and segments depth affecting elements transportation and deposition in the profile, modeling results after 10000 years were confronted with measurements of two soil profiles in loess plateau of China, The simulated trends of organic carbon and CaCO3 in the profile are similar to measured values. Relative sensitivity analysis for carbon cycle process have been done and the results show that the change of organic carbon in long time scale is more sensitive to precipitation, temperature, plant carbon input and decomposition parameters (decomposition rate of humus, ratio of CO2/(BIO+HUM), etc.) in the model. As for the inorganic carbon cycle, precipitation and potential evaporation are important for simulation quality, while the leaching and deposition of CaCO3 are not sensitive to pCO2 and temperature of atmosphere.</p> </li> <li> <p><a target="_blank" rel="noopener noreferrer" onclick="trackOutboundLink('https://www.osti.gov/servlets/purl/967755','SCIGOV-STC'); return false;" href="https://www.osti.gov/servlets/purl/967755"><span>A Brief Review of the Application of 14C in Terrestrial Carbon Cycle Studies</span></a></p> <p><a target="_blank" rel="noopener noreferrer" href="http://www.osti.gov/search">DOE Office of Scientific and Technical Information (OSTI.GOV)</a></p> <p>Guilderson, T; Mcfarlane, K</p> <p>2009-10-22</p> <p>An over-arching goal of the DOE TCP program is to understand the mechanistic controls over the fate, transport, and residence time of carbon in the terrestrial biosphere. Many of the modern process and modeling studies focus on seasonal to interannual variability. However, much of the carbon on the landscape and in soils is in separate reservoirs with turnover times that are multi-decadal to millennial. It is the controls on these longer term pools or reservoirs that is a critical unknown in the face of rising GHGs and climate change and uncertainties of the terrestrial biosphere as a future global sinkmore » or source of atmospheric CO{sub 2} [eg., Friedlingstein et al., 2006; Govindasamy et al., 2005; Thompson et al., 2004]. Radiocarbon measurements, in combination with other data, can provide insight into, and constraints on, terrestrial carbon cycling. Radiocarbon (t{sub 1/2} 5730yrs) is produced naturally in the stratosphere when secondary neutrons generated by cosmic rays collide with {sup 14}N atoms [Libby 1946; Arnold and Libby, 1949]. Upon formation, {sup 14}C is rapidly oxidized to CO and then to CO{sub 2}, and is incorporated into the carbon cycle. Due to anthropogenic activities, the amount of {sup 14}C in the atmosphere doubled in the mid/late 1950s and early 1960s from its preindustrial value of {sup 14}C/{sup 12}C ratio of 1.18 x 10{sup -12} [eg., Nydal and Lovseth, 1983]. Following the atmospheric weapons test ban in 1963, the {sup 14}C/{sup 12}C ratio, has decreased due to the net isotopic exchange between the ocean and terrestrial biosphere [eg., Levin and Hessheimer, 2000] and a dilution effect due to the burning of {sup 14}C-free fossil fuel carbon, the 'Suess Effect' [Suess, 1955]. In the carbon cycle literature, radiocarbon measurements are generally reported as {Delta}{sup 14}C, which includes a correction for mass dependent fractionation [Stuiver and Polach, 1977]. In the context of carbon cycle studies radiocarbon measurements can be used to determine the 'age' and rate of change of carbon stocks or as a biogeochemical tracer to elucidate processes and pathways. It is this dual nature that can be exploited across scales in space (individual plant, plot or research site, ecosystem, regional, and global) and time (days to millennia). For example, across regional scales, {Delta}{sup 14}C measurements of atmosphere CO{sub 2} can be used to attribute carbon dioxide to sources (e.g., respiration vs. fossil fuel emissions) or sinks ( e.g,. photosynthesis), which cannot be readily inferred from concentration, net flux measurements, or {delta}{sup 13}CO{sub 2} [eg. Graven et al., 2009; Levin and Hessheimer, 2000; Turnbull et al., 2007]. At smaller scales, similar analyses can be used to elucidate the source, and 'age' of the below ground component undergoing heterotrophic respiration. Net (biome or ecosystem) uptake of carbon is the difference of two large fluxes: photosynthesis and respiration. Carbon fixation by photosynthesis is, to a large extent, a single process with theoretical underpinnings. On the other-hand, net ecosystem or biome respiration integrates microbial (heterotrophic) and plant (autotrophic) respiration. Eddy covariance methods can be used to estimate bulk CO{sub 2} fluxes but they cannot discriminate the process nor the source of the respired CO{sub 2}. It is these processes that are parameterized in predictive models and contribute to the uncertainty in the climate forcing effect of the carbon cycle in the future [Friedlingstein et al., 2006; Heimann and Reichstein, 2008].« less</p> </li> <li> <p><a target="_blank" rel="noopener noreferrer" onclick="trackOutboundLink('https://www.gpo.gov/fdsys/pkg/CFR-2012-title40-vol10/pdf/CFR-2012-title40-vol10-part63-subpartU-app7.pdf','CFR2012'); return false;" href="https://www.gpo.gov/fdsys/pkg/CFR-2012-title40-vol10/pdf/CFR-2012-title40-vol10-part63-subpartU-app7.pdf"><span>40 CFR Table 7 to Subpart U of... - Operating Parameters for Which Monitoring Levels Are Required To Be Established for Continuous...</span></a></p> <p><a target="_blank" rel="noopener noreferrer" href="http://www.gpo.gov/fdsys/browse/collectionCfr.action?selectedYearFrom=2012&page.go=Go">Code of Federal Regulations, 2012 CFR</a></p> <p></p> <p>2012-07-01</p> <p>.... Condenser Exit temperature Maximum temperature. Carbon adsorber Total regeneration steam flow or nitrogen flow, or pressure (gauge or absolute) a during carbon bed regeneration cycle; and temperature of the carbon bed after regeneration (and within 15 minutes of completing any cooling cycle(s)) Maximum flow or...</p> </li> <li> <p><a target="_blank" rel="noopener noreferrer" onclick="trackOutboundLink('https://www.gpo.gov/fdsys/pkg/CFR-2010-title40-vol11/pdf/CFR-2010-title40-vol11-part63-subpartPPP-app7.pdf','CFR'); return false;" href="https://www.gpo.gov/fdsys/pkg/CFR-2010-title40-vol11/pdf/CFR-2010-title40-vol11-part63-subpartPPP-app7.pdf"><span>40 CFR Table 7 to Subpart Ppp of... - Process Vents From Continuous Unit Operations-Monitoring, Recordkeeping, and Reporting Requirements</span></a></p> <p><a target="_blank" rel="noopener noreferrer" href="http://www.gpo.gov/fdsys/browse/collectionCfr.action?selectedYearFrom=2010&page.go=Go">Code of Federal Regulations, 2010 CFR</a></p> <p></p> <p>2010-07-01</p> <p>... absorbent is used. Condenser Exit temperature Maximum temperature. Carbon adsorber Total regeneration stream mass or volumetric flow during carbon bed regeneration cycle; and temperature of the carbon bed after regeneration (and within 15 minutes of completing any cooling cycle(s)) Maximum mass or volumetric flow; and...</p> </li> <li> <p><a target="_blank" rel="noopener noreferrer" onclick="trackOutboundLink('https://www.gpo.gov/fdsys/pkg/CFR-2011-title40-vol11/pdf/CFR-2011-title40-vol11-part63-subpartPPP-app5.pdf','CFR2011'); return false;" href="https://www.gpo.gov/fdsys/pkg/CFR-2011-title40-vol11/pdf/CFR-2011-title40-vol11-part63-subpartPPP-app5.pdf"><span>40 CFR Table 5 to Subpart Ppp of... - Process Vents From Batch Unit Operations-Monitoring, Recordkeeping, and Reporting Requirements</span></a></p> <p><a target="_blank" rel="noopener noreferrer" href="http://www.gpo.gov/fdsys/browse/collectionCfr.action?selectedYearFrom=2011&page.go=Go">Code of Federal Regulations, 2011 CFR</a></p> <p></p> <p>2011-07-01</p> <p>... Carbon Adsorber f Total regeneration stream mass or volumetric flow during carbon bed regeneration cycle(s), and 1. Record of total regeneration stream mass or volumetric flow for each carbon bed regeneration cycle.2. Record and report the total regeneration stream mass or volumetric flow during each...</p> </li> <li> <p><a target="_blank" rel="noopener noreferrer" onclick="trackOutboundLink('https://www.gpo.gov/fdsys/pkg/CFR-2014-title40-vol10/pdf/CFR-2014-title40-vol10-part63-subpartU-app7.pdf','CFR2014'); return false;" href="https://www.gpo.gov/fdsys/pkg/CFR-2014-title40-vol10/pdf/CFR-2014-title40-vol10-part63-subpartU-app7.pdf"><span>40 CFR Table 7 to Subpart U of... - Operating Parameters for Which Monitoring Levels Are Required To Be Established for Continuous...</span></a></p> <p><a target="_blank" rel="noopener noreferrer" href="http://www.gpo.gov/fdsys/browse/collectionCfr.action?selectedYearFrom=2014&page.go=Go">Code of Federal Regulations, 2014 CFR</a></p> <p></p> <p>2014-07-01</p> <p>.... Condenser Exit temperature Maximum temperature. Carbon adsorber Total regeneration steam flow or nitrogen flow, or pressure (gauge or absolute) a during carbon bed regeneration cycle; and temperature of the carbon bed after regeneration (and within 15 minutes of completing any cooling cycle(s)) Maximum flow or...</p> </li> <li> <p><a target="_blank" rel="noopener noreferrer" onclick="trackOutboundLink('https://www.gpo.gov/fdsys/pkg/CFR-2012-title40-vol12/pdf/CFR-2012-title40-vol12-part63-subpartPPP-app7.pdf','CFR2012'); return false;" href="https://www.gpo.gov/fdsys/pkg/CFR-2012-title40-vol12/pdf/CFR-2012-title40-vol12-part63-subpartPPP-app7.pdf"><span>40 CFR Table 7 to Subpart Ppp of... - Process Vents From Continuous Unit Operations-Monitoring, Recordkeeping, and Reporting Requirements</span></a></p> <p><a target="_blank" rel="noopener noreferrer" href="http://www.gpo.gov/fdsys/browse/collectionCfr.action?selectedYearFrom=2012&page.go=Go">Code of Federal Regulations, 2012 CFR</a></p> <p></p> <p>2012-07-01</p> <p>... absorbent is used. Condenser Exit temperature Maximum temperature. Carbon adsorber Total regeneration stream mass or volumetric flow during carbon bed regeneration cycle; and temperature of the carbon bed after regeneration (and within 15 minutes of completing any cooling cycle(s)) Maximum mass or volumetric flow; and...</p> </li> <li> <p><a target="_blank" rel="noopener noreferrer" onclick="trackOutboundLink('https://www.gpo.gov/fdsys/pkg/CFR-2012-title40-vol12/pdf/CFR-2012-title40-vol12-part63-subpartPPP-app5.pdf','CFR2012'); return false;" href="https://www.gpo.gov/fdsys/pkg/CFR-2012-title40-vol12/pdf/CFR-2012-title40-vol12-part63-subpartPPP-app5.pdf"><span>40 CFR Table 5 to Subpart Ppp of... - Process Vents From Batch Unit Operations-Monitoring, Recordkeeping, and Reporting Requirements</span></a></p> <p><a target="_blank" rel="noopener noreferrer" href="http://www.gpo.gov/fdsys/browse/collectionCfr.action?selectedYearFrom=2012&page.go=Go">Code of Federal Regulations, 2012 CFR</a></p> <p></p> <p>2012-07-01</p> <p>... Carbon Adsorber f Total regeneration stream mass or volumetric flow during carbon bed regeneration cycle(s), and 1. Record of total regeneration stream mass or volumetric flow for each carbon bed regeneration cycle.2. Record and report the total regeneration stream mass or volumetric flow during each...</p> </li> <li> <p><a target="_blank" rel="noopener noreferrer" onclick="trackOutboundLink('https://www.gpo.gov/fdsys/pkg/CFR-2010-title40-vol11/pdf/CFR-2010-title40-vol11-part63-subpartPPP-app5.pdf','CFR'); return false;" href="https://www.gpo.gov/fdsys/pkg/CFR-2010-title40-vol11/pdf/CFR-2010-title40-vol11-part63-subpartPPP-app5.pdf"><span>40 CFR Table 5 to Subpart Ppp of... - Process Vents From Batch Unit Operations-Monitoring, Recordkeeping, and Reporting Requirements</span></a></p> <p><a target="_blank" rel="noopener noreferrer" href="http://www.gpo.gov/fdsys/browse/collectionCfr.action?selectedYearFrom=2010&page.go=Go">Code of Federal Regulations, 2010 CFR</a></p> <p></p> <p>2010-07-01</p> <p>... Carbon Adsorber f Total regeneration stream mass or volumetric flow during carbon bed regeneration cycle(s), and 1. Record of total regeneration stream mass or volumetric flow for each carbon bed regeneration cycle.2. Record and report the total regeneration stream mass or volumetric flow during each...</p> </li> <li> <p><a target="_blank" rel="noopener noreferrer" onclick="trackOutboundLink('https://www.gpo.gov/fdsys/pkg/CFR-2011-title40-vol11/pdf/CFR-2011-title40-vol11-part63-subpartPPP-app7.pdf','CFR2011'); return false;" href="https://www.gpo.gov/fdsys/pkg/CFR-2011-title40-vol11/pdf/CFR-2011-title40-vol11-part63-subpartPPP-app7.pdf"><span>40 CFR Table 7 to Subpart Ppp of... - Process Vents From Continuous Unit Operations-Monitoring, Recordkeeping, and Reporting Requirements</span></a></p> <p><a target="_blank" rel="noopener noreferrer" href="http://www.gpo.gov/fdsys/browse/collectionCfr.action?selectedYearFrom=2011&page.go=Go">Code of Federal Regulations, 2011 CFR</a></p> <p></p> <p>2011-07-01</p> <p>... absorbent is used. Condenser Exit temperature Maximum temperature. Carbon adsorber Total regeneration stream mass or volumetric flow during carbon bed regeneration cycle; and temperature of the carbon bed after regeneration (and within 15 minutes of completing any cooling cycle(s)) Maximum mass or volumetric flow; and...</p> </li> <li> <p><a target="_blank" rel="noopener noreferrer" onclick="trackOutboundLink('https://www.gpo.gov/fdsys/pkg/CFR-2010-title40-vol9/pdf/CFR-2010-title40-vol9-part63-subpartU-app7.pdf','CFR'); return false;" href="https://www.gpo.gov/fdsys/pkg/CFR-2010-title40-vol9/pdf/CFR-2010-title40-vol9-part63-subpartU-app7.pdf"><span>40 CFR Table 7 to Subpart U of... - Operating Parameters for Which Monitoring Levels Are Required To Be Established for Continuous...</span></a></p> <p><a target="_blank" rel="noopener noreferrer" href="http://www.gpo.gov/fdsys/browse/collectionCfr.action?selectedYearFrom=2010&page.go=Go">Code of Federal Regulations, 2010 CFR</a></p> <p></p> <p>2010-07-01</p> <p>.... Condenser Exit temperature Maximum temperature. Carbon adsorber Total regeneration steam flow or nitrogen flow, or pressure (gauge or absolute) a during carbon bed regeneration cycle; and temperature of the carbon bed after regeneration (and within 15 minutes of completing any cooling cycle(s)) Maximum flow or...</p> </li> </ol> <div class="pull-right"> <ul class="pagination"> <li><a href="#" onclick='return showDiv("page_1");'>«</a></li> <li><a href="#" onclick='return showDiv("page_21");'>21</a></li> <li><a href="#" onclick='return showDiv("page_22");'>22</a></li> <li><a href="#" onclick='return showDiv("page_23");'>23</a></li> <li class="active"><span>24</span></li> <li><a href="#" onclick='return showDiv("page_25");'>25</a></li> <li><a href="#" onclick='return showDiv("page_25");'>»</a></li> </ul> </div> </div><!-- col-sm-12 --> </div><!-- row --> </div><!-- page_24 --> <div id="page_25" class="hiddenDiv"> <div class="row"> <div class="col-sm-12"> <div class="pull-right"> <ul class="pagination"> <li><a href="#" onclick='return showDiv("page_1");'>«</a></li> <li><a href="#" onclick='return showDiv("page_21");'>21</a></li> <li><a href="#" onclick='return showDiv("page_22");'>22</a></li> <li><a href="#" onclick='return showDiv("page_23");'>23</a></li> <li><a href="#" onclick='return showDiv("page_24");'>24</a></li> <li class="active"><span>25</span></li> <li><a href="#" onclick='return showDiv("page_25");'>»</a></li> </ul> </div> </div> </div> <div class="row"> <div class="col-sm-12"> <ol class="result-class" start="481"> <li> <p><a target="_blank" rel="noopener noreferrer" onclick="trackOutboundLink('https://www.gpo.gov/fdsys/pkg/CFR-2011-title40-vol9/pdf/CFR-2011-title40-vol9-part63-subpartU-app7.pdf','CFR2011'); return false;" href="https://www.gpo.gov/fdsys/pkg/CFR-2011-title40-vol9/pdf/CFR-2011-title40-vol9-part63-subpartU-app7.pdf"><span>40 CFR Table 7 to Subpart U of... - Operating Parameters for Which Monitoring Levels Are Required To Be Established for Continuous...</span></a></p> <p><a target="_blank" rel="noopener noreferrer" href="http://www.gpo.gov/fdsys/browse/collectionCfr.action?selectedYearFrom=2011&page.go=Go">Code of Federal Regulations, 2011 CFR</a></p> <p></p> <p>2011-07-01</p> <p>.... Condenser Exit temperature Maximum temperature. Carbon adsorber Total regeneration steam flow or nitrogen flow, or pressure (gauge or absolute) a during carbon bed regeneration cycle; and temperature of the carbon bed after regeneration (and within 15 minutes of completing any cooling cycle(s)) Maximum flow or...</p> </li> <li> <p><a target="_blank" rel="noopener noreferrer" onclick="trackOutboundLink('https://www.gpo.gov/fdsys/pkg/CFR-2013-title40-vol10/pdf/CFR-2013-title40-vol10-part63-subpartU-app7.pdf','CFR2013'); return false;" href="https://www.gpo.gov/fdsys/pkg/CFR-2013-title40-vol10/pdf/CFR-2013-title40-vol10-part63-subpartU-app7.pdf"><span>40 CFR Table 7 to Subpart U of... - Operating Parameters for Which Monitoring Levels Are Required To Be Established for Continuous...</span></a></p> <p><a target="_blank" rel="noopener noreferrer" href="http://www.gpo.gov/fdsys/browse/collectionCfr.action?selectedYearFrom=2013&page.go=Go">Code of Federal Regulations, 2013 CFR</a></p> <p></p> <p>2013-07-01</p> <p>.... Condenser Exit temperature Maximum temperature. Carbon adsorber Total regeneration steam flow or nitrogen flow, or pressure (gauge or absolute) a during carbon bed regeneration cycle; and temperature of the carbon bed after regeneration (and within 15 minutes of completing any cooling cycle(s)) Maximum flow or...</p> </li> <li> <p><a target="_blank" rel="noopener noreferrer" onclick="trackOutboundLink('https://www.fs.usda.gov/treesearch/pubs/48848','TREESEARCH'); return false;" href="https://www.fs.usda.gov/treesearch/pubs/48848"><span>Pervasive drought legacies in forest ecosystems and their implications for carbon cycle models</span></a></p> <p><a target="_blank" rel="noopener noreferrer" href="http://www.fs.usda.gov/treesearch/">Treesearch</a></p> <p>W. R. L. Anderegg; C. Schwalm; F. Biondi; J. J. Camarero; G. Koch; M. Litvak; K. Ogle; J. D. Shaw; E. Shevliakova; A. P. Williams; A. Wolf; E. Ziaco; S. Pacala</p> <p>2015-01-01</p> <p>The impacts of climate extremes on terrestrial ecosystems are poorly understood but important for predicting carbon cycle feedbacks to climate change. Coupled climate-carbon cycle models typically assume that vegetation recovery from extreme drought is immediate and complete, which conflicts with the understanding of basic plant physiology. We examined the recovery of...</p> </li> <li> <p><a target="_blank" rel="noopener noreferrer" onclick="trackOutboundLink('https://www.osti.gov/biblio/22667418-modeling-extragalactic-extinction-through-gamma-ray-burst-afterglows','SCIGOV-STC'); return false;" href="https://www.osti.gov/biblio/22667418-modeling-extragalactic-extinction-through-gamma-ray-burst-afterglows"><span>MODELING EXTRAGALACTIC EXTINCTION THROUGH GAMMA-RAY BURST AFTERGLOWS</span></a></p> <p><a target="_blank" rel="noopener noreferrer" href="http://www.osti.gov/search">DOE Office of Scientific and Technical Information (OSTI.GOV)</a></p> <p>Zonca, Alberto; Mulas, Giacomo; Casu, Silvia</p> <p></p> <p>We analyze extragalactic extinction profiles derived through gamma-ray burst afterglows, using a dust model specifically constructed on the assumption that dust grains are not immutable but respond, time-dependently, to the local physics. Such a model includes core-mantle spherical particles of mixed chemical composition (silicate core, sp{sup 2}, and sp{sup 3} carbonaceous layers), and an additional molecular component in the form of free-flying polycyclic aromatic hydrocarbons. We fit most of the observed extinction profiles. Failures occur for lines of sight, presenting remarkable rises blueward of the bump. We find a tendency for the carbon chemical structure to become more aliphatic withmore » the galactic activity, and to some extent with increasing redshifts. Moreover, the contribution of the molecular component to the total extinction is more important in younger objects. The results of the fitting procedure (either successes and failures) may be naturally interpreted through an evolutionary prescription based on the carbon cycle in the interstellar medium of galaxies.« less</p> </li> <li> <p><a target="_blank" rel="noopener noreferrer" onclick="trackOutboundLink('http://adsabs.harvard.edu/abs/2013ECSS..126...61W','NASAADS'); return false;" href="http://adsabs.harvard.edu/abs/2013ECSS..126...61W"><span>Variations in abundance and size distribution of carbohydrates in the lower Mississippi River, Pearl River and Bay of St Louis</span></a></p> <p><a target="_blank" rel="noopener noreferrer" href="http://adsabs.harvard.edu/abstract_service.html">NASA Astrophysics Data System (ADS)</a></p> <p>Wang, Xuri; Cai, Yihua; Guo, Laodong</p> <p>2013-07-01</p> <p>Riverine export of dissolved and particulate organic matter to the sea is one of the major components in marine carbon cycles, affecting biogeochemical processes in estuarine and coastal regions. However, the detailed composition of organic material and the relative partitioning among the dissolved, colloidal, and particulate phases are poorly quantified. The abundance of carbohydrate species and their partitioning among dissolved, colloidal, and particulate phases were examined in the waters from the lower Mississippi River (MR), the lower Pearl River (PR), and the Bay of St. Louis (BSL). Particulate carbohydrates (PCHO) represented a small fraction of the particulate organic carbon (POC) pool, with 4.7 ± 3.1%, 4.5 ± 2.4% and 1.8 ± 0.83% in the MR, PR, and BSL, respectively. Dissolved carbohydrates (DCHO) were a major component of the bulk dissolved organic carbon (DOC) pool, comprising 23%, 35%, and 18% in the MR, PR, and BSL, respectively. Differences in the DCHO/DOC ratio between the MR, PR, and BSL were related to their distinct characteristics in drainage basins, anthropogenic impacts, and hydrological conditions, reflecting differences in sources and composition of organic matter in different aquatic environments. Within the total carbohydrates (TCHO) pool, the high-molecular-weight carbohydrates (HMW-CHO, 1 kDa-0.45 μm) were the dominant species, representing 52-71% of the TCHO pool, followed by the low-molecular-weight carbohydrates (LMW-CHO, <1 kDa), representing 14-44% of the TCHO. The PCHO accounted for 4-16% of the bulk TCHO. Variations in the size distribution of carbohydrates among the MR, PR, and BSL were closely linked to the cycling pathway of organic matter and the interactions between different size fractions of the carbohydrates.</p> </li> <li> <p><a target="_blank" rel="noopener noreferrer" onclick="trackOutboundLink('http://adsabs.harvard.edu/abs/2013AGUFMGC31C1070N','NASAADS'); return false;" href="http://adsabs.harvard.edu/abs/2013AGUFMGC31C1070N"><span>Lessons from forest FACE experiments provide guidance for Amazon-FACE science plan (Invited)</span></a></p> <p><a target="_blank" rel="noopener noreferrer" href="http://adsabs.harvard.edu/abstract_service.html">NASA Astrophysics Data System (ADS)</a></p> <p>Norby, R. J.; Lapola, D. M.</p> <p>2013-12-01</p> <p>Free-air CO2 enrichment (FACE) experiments have provided novel insights into the ecological mechanisms controlling the cycling and storage of carbon in terrestrial ecosystems, and they provide a strong foundation for next-generation experiments in unexplored biomes. Specific lessons from FACE experiments include: (1) Carbon cycle responses are time-dependent because component processes have different rate constants: for example, net primary productivity is increased by elevated CO2, but the response may diminish with time as N cycling feedbacks become important. (2) Carbon partitioning patterns determine the fate of the extra C taken up by CO2-enriched plants, but partitioning responses remain an important challenge for ecosystem models. (3) The influence of N cycling on plant and ecosystem C cycling continues to be a critical uncertainty, and new experiments, especially in the tropics, must also consider P cycling. (4) Plant community structure can influence the ecosystem response to elevated CO2, but dynamic vegetation effects have not been adequately addressed. These experiences from FACE experiments in temperate forests are now guiding the development of a science plan for a FACE experiment in Amazonia. Models and small-scale experimental results agree that elevated CO2 will affect the metabolism of tropical ecosystems, but the qualitative and quantitative expression of the effects are largely unknown, representing a major source of uncertainty that limits our capacity to assess the vulnerability of the Amazon forest to climate change. Recognizing the high importance of the forests of the Amazon basin on global carbon, water, and energy cycles, biodiversity conservation, and the provision of essential services in Latin America, a consortium of Brazilian researchers and international collaborators have developed a science plan for Amazon-FACE. While the challenges presented both by infrastructure needs (roads, electricity, and provision of CO2) and biology (the size and diversity of the forest) are substantial, preliminary evaluation and past experience from temperate forest FACE experiments have supported the feasibility of an experiment comprising replicated 30-m diameter FACE plots in primary forest. The proposed site is the ZF2 research area 60 km north of Manaus and administered by Brazil's National Institute for Amazonia Research (INPA). The vegetation is representative of a dominant fraction of the forests occurring in the Amazon basin: old-growth closed-canopy terra firme (non-flooded) forest with trees 30-35 m in height on well drained clay soils. The major science questions guiding the experiment are closely informed by results of past FACE experiment and involve carbon metabolism, water use, nutrient cycling, interactions with environmental stressors, and the relationship between plant functional traits and community composition. FACE experiments can define ecological processes and mechanisms of responses for predictive models of ecosystem response, and models of CO2 response can define critical uncertainties and testable hypotheses for experiments; hence, the Amazon FACE experiment will feature a close integration of modeling and experimental approaches.</p> </li> <li> <p><a target="_blank" rel="noopener noreferrer" onclick="trackOutboundLink('http://adsabs.harvard.edu/abs/2018AIPC.1966b0027G','NASAADS'); return false;" href="http://adsabs.harvard.edu/abs/2018AIPC.1966b0027G"><span>Photocatalytic degradation of textile dye using TiO2-activated carbon nanocomposite</span></a></p> <p><a target="_blank" rel="noopener noreferrer" href="http://adsabs.harvard.edu/abstract_service.html">NASA Astrophysics Data System (ADS)</a></p> <p>Ghosh, Gourab; Basu, Sankhadeep; Saha, Sudeshna</p> <p>2018-05-01</p> <p>Rapid industrialisation has extended the use of dyes in various industrial applications in order to meet the escalating demands on consumer products. The toxicity level of a particular dye is very important due to its diverse effects on the environment and living organisms. Among all the techniques for dye removal, adsorption and photocatalysis are two important processes which are gaining much attention in recent years. In the present study activated carbon (adsorbent), TiO2 nanoparticles (photocatalyst) and their composite were used for dye removal. Prepared samples were characterized using standard characterization techniques such as XRD and SEM. Activated carbon was prepared from waste shells of Sterculia foetida. Mixture of activated carbon (activation temperature 600°C) and titania (calcined at 500°C) in the ratio 1:1 displayed greater dye removal efficiency than its individual components. Reusability study indicated that the mixture could effectively be used without further regeneration as very little loss in efficiency was observed after single cycle use.</p> </li> <li> <p><a target="_blank" rel="noopener noreferrer" onclick="trackOutboundLink('https://www.ncbi.nlm.nih.gov/pubmed/19565784','PUBMED'); return false;" href="https://www.ncbi.nlm.nih.gov/pubmed/19565784"><span>[Environmental behavior and effect of biomass-derived black carbon in soil: a review].</span></a></p> <p><a target="_blank" rel="noopener noreferrer" href="https://www.ncbi.nlm.nih.gov/entrez/query.fcgi?DB=pubmed">PubMed</a></p> <p>Liu, Yu-Xue; Liu, Wei; Wu, Wei-Xiang; Zhong, Zhe-Ke; Chen, Ying-Xu</p> <p>2009-04-01</p> <p>Biomass-derived black carbon, also named biochar, has the characteristics of high stability against decay and high capability of adsorption, and can affect the environment through its interactions with climate and geology, playing a significant role in global climate change, carbon biogeochemical cycle, and environmental system. In recent years, more and more researchers in the fields of atmospheric sciences, geology, and environmental science focused on the environmental behavior and effect of biochar. As one possible source of the components with high aromatic structure in soil humus, biochar is of great importance in increasing soil carbon storage and improving soil fertility, and in maintaining the balance of soil ecosystem. This paper offered the latest information regarding the characteristics and biotic and abiotic oxidation mechanisms of biochar, its effects on global climate change, and the environmental effect of biochar in soil. Research prospects were briefly discussed on the environmental behavior and effect of biochar in soil ecosystem.</p> </li> <li> <p><a target="_blank" rel="noopener noreferrer" onclick="trackOutboundLink('https://www.ncbi.nlm.nih.gov/pubmed/28621041','PUBMED'); return false;" href="https://www.ncbi.nlm.nih.gov/pubmed/28621041"><span>Extraordinarily Stretchable All-Carbon Collaborative Nanoarchitectures for Epidermal Sensors.</span></a></p> <p><a target="_blank" rel="noopener noreferrer" href="https://www.ncbi.nlm.nih.gov/entrez/query.fcgi?DB=pubmed">PubMed</a></p> <p>Cai, Yichen; Shen, Jie; Dai, Ziyang; Zang, Xiaoxian; Dong, Qiuchun; Guan, Guofeng; Li, Lain-Jong; Huang, Wei; Dong, Xiaochen</p> <p>2017-08-01</p> <p>Multifunctional microelectronic components featuring large stretchability, high sensitivity, high signal-to-noise ratio (SNR), and broad sensing range have attracted a huge surge of interest with the fast developing epidermal electronic systems. Here, the epidermal sensors based on all-carbon collaborative percolation network are demonstrated, which consist 3D graphene foam and carbon nanotubes (CNTs) obtained by two-step chemical vapor deposition processes. The nanoscaled CNT networks largely enhance the stretchability and SNR of the 3D microarchitectural graphene foams, endowing the strain sensor with a gauge factor as high as 35, a wide reliable sensing range up to 85%, and excellent cyclic stability (>5000 cycles). The flexible and reversible strain sensor can be easily mounted on human skin as a wearable electronic device for real-time and high accuracy detecting of electrophysiological stimuli and even for acoustic vibration recognition. The rationally designed all-carbon nanoarchitectures are scalable, low cost, and promising in practical applications requiring extraordinary stretchability and ultrahigh SNRs. © 2017 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.</p> </li> <li> <p><a target="_blank" rel="noopener noreferrer" onclick="trackOutboundLink('https://www.osti.gov/pages/biblio/1329887-carbon-corrosion-pem-fuel-cells-during-drive-cycle-operation','SCIGOV-DOEP'); return false;" href="https://www.osti.gov/pages/biblio/1329887-carbon-corrosion-pem-fuel-cells-during-drive-cycle-operation"><span>Carbon corrosion in PEM fuel cells during drive cycle operation</span></a></p> <p><a target="_blank" rel="noopener noreferrer" href="http://www.osti.gov/pages">DOE PAGES</a></p> <p>Borup, Rodney L.; Papadias, D. D.; Mukundan, Rangachary; ...</p> <p>2015-09-14</p> <p>One of the major contributors to degradation involves the electrocatalyst, including the corrosion of the carbons used as catalyst supports, which leads to changes in the catalyst layer structure. We have measured and quantified carbon corrosion during drive cycle operation and as a variation of the upper and lower potential limits used during drive cycle operation. The amount of carbon corrosion is exacerbated by the voltage cycling inherent in the drive cycle compared with constant potential operation. The potential gap between upper and lower potentials appears to be more important than the absolute operating potentials in the normal operating potentialmore » regime (0.40V to 0.95V) as changes in the measured carbon corrosion are similar when the upper potential was lower compared to raising the lower potential. Catalyst layer thinning was observed during the simulated drive cycle operation which had an associated decrease in catalyst layer porosity. This catalyst layer thinning is not due solely to carbon corrosion, although carbon corrosion likely plays a role; much of this thinning must be from compaction of the material in the catalyst layer. As a result, the decrease in catalyst layer porosity leads to additional performance losses due to mass transport losses.« less</p> </li> <li> <p><a target="_blank" rel="noopener noreferrer" onclick="trackOutboundLink('http://hdl.handle.net/2060/20060005140','NASA-TRS'); return false;" href="http://hdl.handle.net/2060/20060005140"><span>Thermal Cycling of Thermal Control Paints on Carbon-Carbon and Carbon-Polyimide Composites</span></a></p> <p><a target="_blank" rel="noopener noreferrer" href="http://ntrs.nasa.gov/search.jsp">NASA Technical Reports Server (NTRS)</a></p> <p>Jaworske, Donald A.</p> <p>2006-01-01</p> <p>Carbon-carbon composites and carbon-polyimide composites are being considered for space radiator applications owing to their light weight and high thermal conductivity. For those radiator applications where sunlight will impinge on the surface, it will be necessary to apply a white thermal control paint to minimize solar absorptance and enhance infrared emittance. Several currently available white thermal control paints were applied to candidate carbon-carbon and carbon-polyimide composites and were subjected to vacuum thermal cycling in the range of -100 C to +277 C. The optical properties of solar absorptance and infrared emittance were evaluated before and after thermal cycling. In addition, adhesion of the paints was evaluated utilizing a tape test. The test matrix included three composites: resin-derived carbon-carbon and vapor infiltrated carbon-carbon, both reinforced with pitch-based P-120 graphite fibers, and a polyimide composite reinforced with T-650 carbon fibers, and three commercially available white thermal control paints: AZ-93, Z-93-C55, and YB-71P.</p> </li> <li> <p><a target="_blank" rel="noopener noreferrer" onclick="trackOutboundLink('http://adsabs.harvard.edu/abs/2017EGUGA..1915745K','NASAADS'); return false;" href="http://adsabs.harvard.edu/abs/2017EGUGA..1915745K"><span>Tracking heterotrophic and autotrophic carbon cycling by magnetotactic bacteria in freshwater sediments using DNA stable isotope probing</span></a></p> <p><a target="_blank" rel="noopener noreferrer" href="http://adsabs.harvard.edu/abstract_service.html">NASA Astrophysics Data System (ADS)</a></p> <p>Kürşat Coşkun, Ömer; Roud, Sophie; He, Kuang; Petersen, Nikolai; Gilder, Stuart; Orsi, William D.</p> <p>2017-04-01</p> <p>Magnetotactic bacteria (MTB) are diverse, widespread, motile prokaryotes which biomineralize nanosize magnetic minerals, either magnetite or gregite, under highly conserved genetic control and have magnetotaxis to align their position in aquatic environment according to Earth's magnetic field. They play important roles on some geobiological cycle of important minerals such as iron, sulphur, nitrogen and carbon. Yet, to date, their importance in carbon cycle and carbon source in their natural environment have not been previously studied. In this study, we focused on freshwater benthic carbon cycling of MTB and total bacteria using DNA stable isotope probing (DNA-SIP) technique coupled with quantitative PCR (qPCR). Pond sediments from Unterlippach (Germany) were amended with 13C-labelled sodium bicarbonate and 13C-labelled organic matter, and incubated in the dark over a two week time period. Applying separate qPCR assays specific for total bacteria and MTB, respectively, allowed us to estimate the contribution of MTB to total heterotrophic and autotrophic carbon cycling via DNA-SIP. After one week, there was a slight degree of autotrophic activity which increased markedly after two weeks. Comparing total DNA to the qPCR data revealed that changes in the buoyant density of DNA was due mainly to autotrophic bacterial production. DNA-SIP also identified heterotrophic utilization of 13C-labelled organic matter by MTB after 1 week. The qPCR data also allowed us to estimate uptake rates based on the incubation times for heterotrophic and autotrophic MTB. High-throughput DNA sequencing of 16S rRNA genes showed that most of the MTB involved in carbon cycling were related to the Magnetococcus genus. This study sheds light on the carbon sources for MTB in a natural environment and helps unravel their ecological role in the carbon cycle.</p> </li> <li> <p><a target="_blank" rel="noopener noreferrer" onclick="trackOutboundLink('http://adsabs.harvard.edu/abs/2017AGUFM.B43D2164Y','NASAADS'); return false;" href="http://adsabs.harvard.edu/abs/2017AGUFM.B43D2164Y"><span>Monitoring terrestrial dissolved organic carbon export at land-water interfaces using remote sensing</span></a></p> <p><a target="_blank" rel="noopener noreferrer" href="http://adsabs.harvard.edu/abstract_service.html">NASA Astrophysics Data System (ADS)</a></p> <p>Yu, Q.; Li, J.; Tian, Y. Q.</p> <p>2017-12-01</p> <p>Carbon flux from land to oceans and lakes is a crucial component of carbon cycling. However, this lateral carbon flow at land-water interface is often neglected in the terrestrial carbon cycle budget, mainly because observations of the carbon dynamics are very limited. Monitoring CDOM/DOC dynamics using remote sensing and assessing DOC export from land to water remains a challenge. Current CDOM retrieval algorithms in the field of ocean color are not simply applicable to inland aquatic ecosystems since they were developed for coarse resolution ocean-viewing imagery and less complex water types in open-sea. We developed a new semi-analytical algorithm, called SBOP (Shallow water Bio-Optical Properties algorithm) to adapt to shallow inland waters. SBOP was first developed and calibrated based on in situ hyperspectral radiometer data. Then we applied it to the Landsat-8 OLI images and evaluated the effectiveness of the multispectral images on inversion of CDOM absorption based on our field sampling at the Saginaw Bay in the Lake Huron. The algorithm performances (RMSE = 0.17 and R2 = 0.87 in the Saginaw Bay; R2 = 0.80 in the northeastern US lakes) is promising and we conclude the CDOM absorption can be derived from Landsat-8 OLI image in both optically deep and optically shallow waters with high accuracy. Our method addressed challenges on employing appropriate atmospheric correction, determining bottom reflectance influence for shallow waters, and improving for bio-optical properties retrieval, as well as adapting to both hyperspectral and the multispectral remote sensing imagery. Over 100 Landsat-8 images in Lake Huron, northeastern US lakes, and the Arctic major rivers were processed to understand the CDOM spatio-temporal dynamics and its associated driving factors.</p> </li> <li> <p><a target="_blank" rel="noopener noreferrer" onclick="trackOutboundLink('http://adsabs.harvard.edu/abs/2016AGUFMED41A0813R','NASAADS'); return false;" href="http://adsabs.harvard.edu/abs/2016AGUFMED41A0813R"><span>Optical Characterization and Bioavailability of Dissolved Organic Matter of Leaf Leachates from Restored and Forested Delmarva Bay Catchments</span></a></p> <p><a target="_blank" rel="noopener noreferrer" href="http://adsabs.harvard.edu/abstract_service.html">NASA Astrophysics Data System (ADS)</a></p> <p>Reed, E.; Armstrong, A.</p> <p>2016-12-01</p> <p>The optical properties and lability of fresh leaf and litter leachates obtained from Delmarva wetlands were analyzed to gain a further understanding of the carbon inputs and outputs of that wetland system. Carbon entering the wetland system may be digested by microbes and then given off as either carbon dioxide or methane, both of which enter the atmosphere as greenhouse gases. Delmarva Bays are often considered geographically isolated and only have surface water present in certain times of year. The vegetation around the wetlands are assumed to be a major input of the dissolved organic matter (DOM) in the wetland surface water. An understanding of the sources and lability of wetland water DOM can lead to further insight into the connections between vegetation, wetland management, and carbon cycling. Two paired wetland sites were sampled in this study, each included a forested catchment and a prior-converted agricultural wetland that had undergone hydrological ecosystem restoration. Leaf samples of Liquidambar styraciflua, Acer rubrum, Nyssa sylvatica, Polygonum, and Typha were taken directly from the living plant or from surrounding ground as litter. Spectral properties of the leachates were determined from fluorescence and absorbance, including PARAFAC components, fluorescence index (FI), humification index (HI), and the specific ultraviolet absorbance (SUVA). Leachates were also incubated with microbes taken from Tuckahoe Creek, a stream to which all sampled sites eventually drain, to determine the bioavailability of the carbon. There were measurable differences found between samples obtained from leaves and litter, as well as a difference between the herbaceous and tree samples. The results obtained from this study can help create more accurate models of how carbon cycles through these wetlands, both in forested and restored environments.</p> </li> <li> <p><a target="_blank" rel="noopener noreferrer" onclick="trackOutboundLink('https://www.osti.gov/pages/biblio/1437597-transcript-level-coordination-carbon-pathways-during-silicon-starvation-induced-lipid-accumulation-diatom-thalassiosira-pseudonana','SCIGOV-DOEP'); return false;" href="https://www.osti.gov/pages/biblio/1437597-transcript-level-coordination-carbon-pathways-during-silicon-starvation-induced-lipid-accumulation-diatom-thalassiosira-pseudonana"><span>Transcript level coordination of carbon pathways during silicon starvation-induced lipid accumulation in the diatom Thalassiosira pseudonana</span></a></p> <p><a target="_blank" rel="noopener noreferrer" href="http://www.osti.gov/pages">DOE PAGES</a></p> <p>Smith, Sarah R.; Gle, Corine; Abbriano, Raffaela M.; ...</p> <p>2016-02-04</p> <p>Diatoms are one of the most productive and successful photosynthetic taxa on Earth and possess attributes such as rapid growth rates and production of lipids, making them candidate sources of renewable fuels. Despite their significance, few details of the mechanisms used to regulate growth and carbon metabolism are currently known, hindering metabolic engineering approaches to enhance productivity. To characterize the transcript level component of metabolic regulation, genome-wide changes in transcript abundance were documented in the model diatom Thalassiosira pseudonana on a time-course of silicon starvation. Growth, cell cycle progression, chloroplast replication, fatty acid composition, pigmentation, and photosynthetic parameters were characterizedmore » alongside lipid accumulation. Extensive coordination of large suites of genes was observed, highlighting the existence of clusters of coregulated genes as a key feature of global gene regulation in T. pseudonana. The identity of key enzymes for carbon metabolic pathway inputs (photosynthesis) and outputs (growth and storage) reveals these clusters are organized to synchronize these processes. Coordinated transcript level responses to silicon starvation are probably driven by signals linked to cell cycle progression and shifts in photophysiology. A mechanistic understanding of how this is accomplished will aid efforts to engineer metabolism for development of algal-derived biofuels.« less</p> </li> <li> <p><a target="_blank" rel="noopener noreferrer" onclick="trackOutboundLink('https://www.ncbi.nlm.nih.gov/pubmed/29901246','PUBMED'); return false;" href="https://www.ncbi.nlm.nih.gov/pubmed/29901246"><span>Traits drive global wood decomposition rates more than climate.</span></a></p> <p><a target="_blank" rel="noopener noreferrer" href="https://www.ncbi.nlm.nih.gov/entrez/query.fcgi?DB=pubmed">PubMed</a></p> <p>Hu, Zhenhong; Michaletz, Sean T; Johnson, Daniel J; McDowell, Nate G; Huang, Zhiqun; Zhou, Xuhui; Xu, Chonggang</p> <p>2018-06-14</p> <p>Wood decomposition is a major component of the global carbon cycle. Decomposition rates vary across climate gradients, which is thought to reflect the effects of temperature and moisture on the metabolic kinetics of decomposers. However, decomposition rates also vary with wood traits, which may reflect the influence of stoichiometry on decomposer metabolism as well as geometry relating the surface areas that decomposers colonize with the volumes they consume. In this paper, we combined metabolic and geometric scaling theories to formalize hypotheses regarding the drivers of wood decomposition rates, and assessed these hypotheses using a global compilation of data on climate, wood traits, and wood decomposition rates. Our results are consistent with predictions from both metabolic and geometric scaling theories. Approximately half of the global variation in decomposition rates was explained by wood traits (nitrogen content and diameter), while only a fifth was explained by climate variables (air temperature, precipitation, and relative humidity). These results indicate that global variation in wood decomposition rates is best explained by stoichiometric and geometric wood traits. Our findings suggest that inclusion of wood traits in global carbon cycle models can improve predictions of carbon fluxes from wood decomposition. This article is protected by copyright. All rights reserved. This article is protected by copyright. All rights reserved.</p> </li> <li> <p><a target="_blank" rel="noopener noreferrer" onclick="trackOutboundLink('https://www.ncbi.nlm.nih.gov/pubmed/29772225','PUBMED'); return false;" href="https://www.ncbi.nlm.nih.gov/pubmed/29772225"><span>Maternal one carbon metabolism through increased oxidative stress and disturbed angiogenesis can influence placental apoptosis in preeclampsia.</span></a></p> <p><a target="_blank" rel="noopener noreferrer" href="https://www.ncbi.nlm.nih.gov/entrez/query.fcgi?DB=pubmed">PubMed</a></p> <p>Kasture, Vaishali V; Sundrani, Deepali P; Joshi, Sadhana R</p> <p>2018-05-14</p> <p>Adequate maternal nutrition is critical for a healthy pregnancy outcome and poor maternal nutrition is known to be associated with pregnancy complications like preeclampsia. We have earlier demonstrated that there is an imbalance in the levels of micronutrients (folate and vitamin B 12 ) along with low levels of long chain polyunsaturated fatty acids (LCPUFA) and high homocysteine levels in women with preeclampsia. Homocysteine is known to be involved in the formation of free radicals leading to increased oxidative stress. Higher oxidative stress has been shown to be associated with increased apoptotic markers in the placenta. Preeclampsia is of placental origin and is associated with increased oxidative stress, disturbed angiogenesis and placental apoptosis. The process of angiogenesis is important for placental and fetal development and various angiogenic growth factors inhibit apoptosis by inactivation of proapoptotic proteins through a series of cellular signalling pathways. We propose that an altered one carbon cycle resulting in increased oxidative stress and impaired angiogenesis will contribute to increased placental apoptosis leading to preeclampsia. Understanding the association of one carbon cycle components and the possible mechanisms through which they regulate apoptosis will provide clues for reducing risk of pregnancy complications. Copyright © 2017. Published by Elsevier Inc.</p> </li> <li> <p><a target="_blank" rel="noopener noreferrer" onclick="trackOutboundLink('https://www.osti.gov/pages/biblio/1259376-artificial-photosynthetic-antennas-reaction-centers','SCIGOV-DOEP'); return false;" href="https://www.osti.gov/pages/biblio/1259376-artificial-photosynthetic-antennas-reaction-centers"><span>Artificial photosynthetic antennas and reaction centers</span></a></p> <p><a target="_blank" rel="noopener noreferrer" href="http://www.osti.gov/pages">DOE PAGES</a></p> <p>Llansola-Portoles, Manuel J.; Gust, Devens; Moore, Thomas A.; ...</p> <p>2017-03-01</p> <p>Presently, the world is experiencing an unprecedented crisis associated with the CO2 produced by the use of fossil fuels to power our economies. As evidenced by the increasing levels in the atmosphere, the reduction of CO2 to biomass by photosynthesis cannot keep pace with production with the result that nature has lost control of the global carbon cycle. In order to restore control of the global carbon cycle to solar-driven processes, highly efficient artificial photosynthesis can augment photosynthesis in specific ways and places. The increased efficiency of artificial photosynthesis can provide both renewable carbon-based fuels and lower net atmospheric levelsmore » of CO2, which will preserve land and support the ecosystem services upon which all life on Earth depends. The development of artificial photosynthetic antennas and reaction centers contributes to the understanding of natural photosynthesis and to the knowledge base necessary for the development of future scalable technologies. This review focuses on the design and study of molecular and hybrid molecular-semiconductor nanoparticle based systems, all of which are inspired by functions found in photosynthesis and some of which are inspired by components of photosynthesis. In addition to constructs illustrating energy transfer, photoinduced electron transfer, charge shift reactions and proton coupled electron transfer, our review covers systems that produce proton motive force.« less</p> </li> <li> <p><a target="_blank" rel="noopener noreferrer" onclick="trackOutboundLink('https://www.osti.gov/biblio/1259376-artificial-photosynthetic-antennas-reaction-centers','SCIGOV-STC'); return false;" href="https://www.osti.gov/biblio/1259376-artificial-photosynthetic-antennas-reaction-centers"><span>Artificial photosynthetic antennas and reaction centers</span></a></p> <p><a target="_blank" rel="noopener noreferrer" href="http://www.osti.gov/search">DOE Office of Scientific and Technical Information (OSTI.GOV)</a></p> <p>Llansola-Portoles, Manuel J.; Gust, Devens; Moore, Thomas A.</p> <p></p> <p>Presently, the world is experiencing an unprecedented crisis associated with the CO2 produced by the use of fossil fuels to power our economies. As evidenced by the increasing levels in the atmosphere, the reduction of CO2 to biomass by photosynthesis cannot keep pace with production with the result that nature has lost control of the global carbon cycle. In order to restore control of the global carbon cycle to solar-driven processes, highly efficient artificial photosynthesis can augment photosynthesis in specific ways and places. The increased efficiency of artificial photosynthesis can provide both renewable carbon-based fuels and lower net atmospheric levelsmore » of CO2, which will preserve land and support the ecosystem services upon which all life on Earth depends. The development of artificial photosynthetic antennas and reaction centers contributes to the understanding of natural photosynthesis and to the knowledge base necessary for the development of future scalable technologies. This review focuses on the design and study of molecular and hybrid molecular-semiconductor nanoparticle based systems, all of which are inspired by functions found in photosynthesis and some of which are inspired by components of photosynthesis. In addition to constructs illustrating energy transfer, photoinduced electron transfer, charge shift reactions and proton coupled electron transfer, our review covers systems that produce proton motive force.« less</p> </li> <li> <p><a target="_blank" rel="noopener noreferrer" onclick="trackOutboundLink('https://www.ncbi.nlm.nih.gov/pubmed/29072451','PUBMED'); return false;" href="https://www.ncbi.nlm.nih.gov/pubmed/29072451"><span>Chemical Imaging of Nanoscale Interfacial Inhomogeneity in LiFePO4 Composite Electrodes from a Cycled Large-Format Battery.</span></a></p> <p><a target="_blank" rel="noopener noreferrer" href="https://www.ncbi.nlm.nih.gov/entrez/query.fcgi?DB=pubmed">PubMed</a></p> <p>Zhou, Jigang; Wang, Jian; Hu, Yongfeng; Lu, Mi</p> <p>2017-11-15</p> <p>The nanoscale interfacial inhomogeneity in a cycled large-format LiFePO 4 (LFP) composite electrode has been studied by X-ray photoemission electron microscopy at single particle spatial resolution with a probe depth of ∼5 nm. The loss of active lithium in cycled LFP causes the coexsitence of fully delithiated LFP (FePO 4 ) and partially delithiated LFP (Li 0.6 FePO 4 or Li 0.8 FePO 4 ) as a function of the extent of lithium loss. The distribution of various lithium loss phases along with local agglomeration of LFP and degradation of binder and carbon black are correlatively visualized. This is the first experimental exploration of chemical interplay between components in the composite electrode from a large-format battery, and implications on the LFP degradation in this battery are discussed.</p> </li> </ol> <div class="pull-right"> <ul class="pagination"> <li><a href="#" onclick='return showDiv("page_1");'>«</a></li> <li><a href="#" onclick='return showDiv("page_21");'>21</a></li> <li><a href="#" onclick='return showDiv("page_22");'>22</a></li> <li><a href="#" onclick='return showDiv("page_23");'>23</a></li> <li><a href="#" onclick='return showDiv("page_24");'>24</a></li> <li class="active"><span>25</span></li> <li><a href="#" onclick='return showDiv("page_25");'>»</a></li> </ul> </div> </div><!-- col-sm-12 --> </div><!-- row --> </div><!-- page_25 --> <div class="footer-extlink text-muted" style="margin-bottom:1rem; text-align:center;">Some links on this page may take you to non-federal websites. 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