Evaluation of the recharge processes and impacts of irrigation on groundwater using CFCs and radiogenic isotopes in the Silao-Romita basin, Mexico

The recharge processes in the overexploited aquifer of the Silao Romita basin, central Mexico, were investigated by means of gaseous tracers (chlorofluorocarbons, CFCs) and radioactive isotopes (C-14, tritium). CFC concentrations varied between 0.06 and 12 pmol/l (CFC-11), 0.03 and 1.7 pmol/l (CFC-12), and <0.01 and 0.23 pmol/l (CFC-113). CFC concentrations are controlled by irrigation return flow which became apparent by the comparison with tritium. Tritium activities ranged from 0 to 3.5 TU. The calculated mean residence times of 70 to more than 300 years are considerably lower than the ages estimated based on the CFCs data. These data showed that CFCs were not appropriate for groundwater dating in this particular area but the CFCs were suitable as a qualitative measure of the magnitude of irrigation return flow which proved to be a significant source of recharge in the irrigated areas. Radiocarbon activities were in the range of 6–109 pmC. Carbon-13 values varied between –11.9 and –7.2‰ VPDB. Modelling of carbon isotopes with NETPATH along a plausible flow path reveals considerable influences of exchange with soil CO₂ and carbonate dissolution. Radiocarbon data indicate, at least in one case, the existence of groundwaters with residence times of more than 10,000 years.     

A 17-Year Record of Environmental Tracers in Spring Discharge,Shenandoah National Park,Virginia, USA: Use of Climatic Data and Environmental Conditions to Interpret Discharge,Dissolved Solutes,and Tracer Concentrations

A 17-year record (1995–2012) of a suite of environmental tracer concentrations in discharge from 34 springs located along the crest of the Blue Ridge Mountains in Shenandoah National Park (SNP), Virginia, USA, reveals patterns and trends that can be related to climatic and environmental conditions. These data include a 12-year time series of monthly sampling at five springs, with measurements of temperature, specific conductance, pH, and discharge recorded at 30-min intervals. The monthly measurements include age tracers (CFC-11, CFC-12, CFC-113, CFC-13, SF₆, and SF₅CF₃), dissolved gases (N₂, O₂, Ar, CO₂, and CH₄), stable isotopes of water, and major and trace inorganic constituents. The chlorofluorocarbon (CFC) and sulfur hexafluoride (SF₆₎ concentrations (in pptv) in spring discharge closely follow the concurrent monthly measurements of their atmospheric mixing ratios measured at the Air Monitoring Station at Big Meadows, SNP, indicating waters 0–3 years in age. A 2-year (2001–2003) record of unsaturated zone air displayed seasonal deviations from North American Air of ±10 % for CFC-11 and CFC-113, with excess CFC-11 and CFC-113 in peak summer and depletion in peak winter. The pattern in unsaturated zone soil CFCs is a function of gas solubility in soil water and seasonal unsaturated zone temperatures. Using the increase in the SF₆ atmospheric mixing ratio, the apparent (piston flow) SF₆ age of the water varied seasonally between about 0 (modern) in January and up to 3 years in July–August. The SF₆ concentration and concentrations of dissolved solutes (SiO₂, Ca²⁺, Mg²⁺, Na⁺, Cl^?, and HCO₃ ^?) in spring discharge demonstrate a fraction of recent recharge following large precipitation events. The output of solutes in the discharge of springs minus the input from atmospheric deposition per hectare of watershed area (mol ha^?1 a^?1) were approximately twofold greater in watersheds draining the regolith of Catoctin metabasalts than that of granitic gneisses and granitoid crystalline rocks. The stable isotopic composition of water in spring discharge broadly correlates with the Oceanic Niño Index. Below normal precipitation and enriched stable isotopic composition were observed during El Niño years.     

Decomposing the changes of energy-related carbon emissions in China: evidence from the PDA approach

In order to investigate the main drivers of CO₂ emissions changes in China during the 11th Five-Year Plan period (2006–2010) and seek the main ways to reduce CO₂ emissions, we decompose the changes of energy-related CO₂ emissions using the production-theoretical decomposition analysis approach. The results indicate that, first, economic growth and energy consumption are the two main drivers of CO₂ emissions increase during the sample period; particularly in the northern coastal, northwest and central regions, where tremendous coal resources are consumed, the driving effect of their energy consumption on CO₂ emissions appears fairly evident. Second, the improvement of carbon abatement technology and the reduction in energy intensity play significant roles in curbing carbon emissions, and comparatively the effect of carbon abatement technology proves more significant. Third, energy use technical efficiency, energy use technology and carbon abatement technical efficiency have only slight influence on CO₂ emissions overall. In the end, we put forward some policy recommendations for China’s government to reduce CO₂ emissions intensity in the future.     

Comparative study for environmental performances of traditional manufacturing and directed energy deposition processes

Additive manufacturing is considered more sustainable than traditional manufacturing due to its efficient energy and materials usage. However, previous literature indicates that this suggestion is applicable only for the polymer materials, and the environmental issues of additive manufacturing with metallic materials are still not clear. With the method of life cycle assessment, this paper analyzes and compares the energy consumptions and environmental impacts of direct energy deposition and traditional machining processes for a typical metal part. Further, the article attempts to identify the significant issues in the two manufacturing options that contribute most to the environmental impacts. Six environmental impacts were assessed in this study: global warming potential (GWP); acidification potential (AP); eutrophication potential; ozone depletion potential (ODP); photochemical ozone creation potential (POCP); and abiotic depletion potential (ADP). The results show that the gear laser fabrication process consumes more energy and releases more negative emissions compared with traditional gear manufacturing processes. The results of GWP, AP, ODP, ADP and POCP of the traditional gear manufacturing are only 30.33, 43.42, 17, 65.05 and 54.68% of the gear laser fabrication.     

Black carbon and organic carbon emissions from wildfires in Mexico

In Mexico, approximately 7650 wildfires occur annually, affecting 263 115 hectares of land. In addition to their impact on land degradation, wildfires cause deforestation, damage to ecosystems and promote land use change; apart from being the source of emissions of toxic substances to the environment (i.e., hydrogen cyanide, black carbon and organic carbon). Black carbon is a short-lived greenhouse pollutant that also promotes snow and ice melting and decreased rainfall; it has an estimated global warming potential close to 5000.¹ We present an estimate of the black carbon and organic carbon emissions from wildfires in Mexico from 2000 to 2012 using selected emission factors from the literature and activity data from local agencies. The results show average emissions of 5955 Mg/yr for black carbon and 62 085 Mg/yr for organic carbon. Black carbon emissions are estimated to be 14 888 Gg CO₂ equivalent (CO₂ eq) per year on average. With proper management of wildfires, such emissions can be mitigated. Moreover, improved air quality, conservation of ecosystems, improvement of visibility and maintenance of land use are a subset of the related co-benefits. Mitigating forest organic carbon emissions, which are ten times higher than black carbon emissions, would also prevent the morbidity and mortality impacts of toxic organic compounds in the environment.     

Use and application of CFC-11,CFC-12,CFC-113 and SF_6 as environmental tracers of groundwater residence time:A review

Groundwater residence time is a fundamental property of groundwater to understand important hydrogeological issues,such as deriving sustainable abstraction volumes,or,the evolution of groundwater quality.The anthropogenic trace gases chlorofluorocarbons(CFC-11,CFC-12 and CFC-113)and sulphur hexafluoride(SF_6)are ideal in this regard because they have been released globally at known rates and become dissolved in groundwater following Henry's Law,integrating over large spatial(global)and temporal(decades)scales.The CFCs and SF_6 are able to date groundwater up to～100 years old with the caveat of certain simplifying assumptions.However,the inversion of environmental tracer concentrations(CFCs and SF_6)to derive groundwater age rests on the accurate determination of groundwater recharge parameters,namely temperature,elevation,salinity and excess air,in addition to resolving the potential for contamination,degradation and unsaturated zone effects.This review explores the fundamentals of CFC-11,CFC-12,CFC-113 and SF_6 as environmental tracers of groundwater age and recommends complementary techniques throughout.Once this relatively simple and inexpensive technique has been used to determine initial concentrations at the recharge zone,setting the groundwater dating'clock' to zero,this review then explores the meaning of groundwater'age' in relation to measured environmental tracer concentrations.It is shown that the CFCs and SF_6 may be applied to a wide-range of hydrogeological problems and suggests that environmental tracers are particularly powerful tools when integrated with numerical flow and transport models.     

Rate measurements and detection of gas microseepage to the atmosphere from an enhanced oil recovery/sequestration project,Rangely, Colorado,USA

One of the proposals for large-scale sequestration of fossil fuel-derived CO₂ is deep geologic disposal in depleted oil/gas reservoirs or deep aquifers. Previously published scenarios for this inadequately proven technology have either ignored or dismissed the possibility of vertical migration of gases caused by overpressure. Overpressuring of a reservoir or aquifer will be necessary in order to have acceptable rates for dispersal of injected CO₂. This research describes methodology and the results of measurement of microseepage of CO₂ and CH₄ at a large-scale CO₂-enhanced oil recovery (EOR) operation at Rangely, Colorado, USA. Shallow and deep soil gas concentrations, and direct transport of CO₂ and CH₄ into the atmosphere were measured. The interpretation of the measurements was complemented by both stable and radiogenic isotopic measurements of C. The results have demonstrated an estimated microseepage to the atmosphere of approximately 400 metric tonnes of CH₄/a from the 78 km² area of the Rangely field. Preliminary estimates of deep-sourced CO₂ losses are <3800 tonnes/a, based on stable isotope measurements of soil gases. Several holes up to 10 m deep were drilled on, and off the field for nested gas sampling of composition and stable C isotopic ratios for CO₂ and CH₄. Carbon-14 measurements on CO₂ from these holes indicate that deep-sourced CO₂ microseepage losses were approximately 170 tonnes/a.     

Effects of nitrogen on the ecosystem respiration,CH<Subscript>4</Subscript> and N<Subscript>2</Subscript>O emissions to the atmosphere from the freshwater marshes in northeast China

Freshwater marshes could be a source of greenhouse gases emission because they contain large amounts of soil carbon and nitrogen. These emissions are strongly influenced by exogenous nitrogen. We investigate the effects of exogenous nitrogen on ecosystem respiration (CO₂), CH₄ and N₂O emissions from freshwater marshes in situ in the Sanjiang Plain Northeast of China during the growing seasons of 2004 and 2005, using a field fertilizer experiment and the static opaque chamber/GC techniques. The results show that there were no significant differences in patterns of seasonal variations of CO₂ and CH₄ among the fertilizer and non-fertilizer treatments, but the seasonal patterns of N₂O emission were significantly influenced by the exogenous nitrogen. Seasonal averages of the CO₂ flux from non-fertilizer and fertilizer were 987.74 and 1,344.35 mg m ⁻² h ⁻¹, respectively, in 2004, and 898.59 and 2,154.17 mg m ⁻² h ⁻¹, respectively, in 2005. And the CH₄ from the control and fertilizer treatments were 6.05 and 13.56 mg m ⁻² h ⁻¹ and 0.72 and 1.88 mg m ⁻² h ⁻¹, respectively, in 2004 and 2005. The difference of N₂O flux between the fertilizer and non-fertilizer treatments is also significant either in 2004 and 2005. On the time scale of 20-, 100-, and 500-year periods, the integrated global warming potential (GWP) of CO₂ + CH₄ + N₂O released during the two growing seasons for the treatment of fertilizer was 97, 94 and 89%, respectively, higher than that for the control, which suggested that the nitrogen fertilizer can enhance the GWP of the CH₄ and N₂O either in long time or short time scale.     

Accuracy of CFC groundwater dating in a crystalline bedrock aquifer: Data from a site in southern Sweden

The concentrations of chlorofluorocarbons (CFC-11, CFC-12, and CFC-113) and tritium were determined in groundwater in fractured crystalline bedrock at Finnsjön, Sweden. The specific goal was to investigate the accuracy of CFC dating in such an environment, taking potential degradation and mixing of water into consideration. The water was sampled to a depth of 42 m in three boreholes along an 800-m transect, from a recharge area to a local discharge area. The CFC-113 concentration was at the detection limit in most samples. The apparent recharge date obtained from CFC-11 was earlier than from CFC-12 for all samples, with a difference of over 20 years for some samples. The difference was probably caused by degradation of CFC-11. The CFC-12 dating of the samples ranged from before 1945 to 1975, with the exception of a sample from the water table, which had a present-day concentration. Conclusions about flow paths or groundwater velocity could not be drawn from the CFCs. The comparison between CFC-12 and tritium concentrations showed that most samples could be unmixed or mixtures of waters with different ages, and the binary mixtures that matched the measured concentrations were determined. The mixing model approach can be extended with additional tracers.

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Resumen Precisión en la datación de aguas subterráneas utilizando CFC en un acuífero de rocas cristalinas: datos provenientes de un sitio al sur de Suecia.Se determinaron las concentraciones de clorofluorucarbonos (CFC-11, CFC-12, y CFC-113) y de tritio en aguas subterráneas alojadas en rocas cristalinas fracturadas de Finnsjön, Suecia. El objetivo específico consistió en investigar la precisión de la datación de aguas subterráneas con CFC en este tipo de ambiente, tomando en consideración la degradación potencial y la mezcla de agua. Las muestras de agua se tomaron a una profundidad de 42 m en tres pozos ubicados a lo largo de una línea de 800 m transversal a una zona de recarga y de zona de descarga local. En la mayoría de las muestras se encontró que la concentración de CFC-113 estuvo en el límite de detección. La edad que se estimó en todas las muestras para la recarga aparente en base a CFC-11 fue más joven que la edad proveniente de CFC-12, con una diferencia de más de 20 años para algunas muestras. Esta diferencia fue causada probablemente por la degradación del CFC-11. La datación CFC-12 de las muestras varió de antes de 1945 a 1975, con la excepción de una muestra tomada en el nivel freático, la cual presentó concentración actual. No fue posible obtener conclusiones acerca de las trayectorias de flujo o la velocidad de agua subterránea a partir de los CFCs. La comparación entre las concentraciones de CFC-12 y tritio mostró que la mayoría de las muestras pueden tener composición sencilla o bien consistir de mezclas de aguas de diferentes edades. Esta comparación también permitió determinar las mezclas binarias que corresponden a las concentraciones medidas. Pueden utilizarse trazadores adicionales para ampliar el modelo de mezclas propuesto.

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Résumé Précision de la datation au CFC dans un aquifère rocheux-fracturé: données dun site du sud de la Suède.Les concentrations en chlorofluorocarbones (CFC-11, CFC-12, CFC-113) et entritium ont été déterminées dans leau souterraine dun massif fracturé à Finnsjön en Suède. Le but de cette étude est de mieux cerner la précision de la méthode de datation au CFC dans ce type denvironnement hydrogéologique, tout en considérant déventuels phénomènes de dégradation et de mélange deaux. Leau a été échantillonnée à une profondeur de 42 mètres dans trois forages alignés sur 800 mètres entre une zone de recharge et une zone de déversement. Les concentrations en CFC-113 sont dans la plupart des échantillons à la limite de détection. Pour tous les échantillons, la date de la recharge établie avec le CFC-11 est antérieure à la date établie avec le CFC-12. La différence entre les deux dates peut dépasser 20 ans et sexplique—probablement—par la dégradation du CFC-11. Les dates de recharge de la nappe mesurées au CFC-12 sont comprises entre 1945 et 1975, excepté pour un échantillon qui possède une concentration actuelle. Il nest pas possible de tirer des conclusions concernant la direction des écoulements et la vitesse de leau souterraine. La comparaison entre CFC-12 et tritium montre que des échantillons pourraient être soit le résultat du mélange deaux dâges différents, soit des échantillons non-mélangés. Dans le cas dun mélange binaire, les rapports du mélange composant la concentration mesurée sont déterminés. Lapproche par modèle de mélange peut être étendue à des traceurs additionnels.

     

Computer modeling of methanotrophic oxidation of hydrocarbons in the unsaturated zone from an enhanced oil recovery/sequestration project, Rangely, Colorado, USA

One of the proposals for large-scale sequestration of fossil fuel-derived CO₂ is deep geologic disposal in depleted oil/gas reservoirs or deep aquifers. Previously published scenarios for this inadequately proven technology have either ignored or dismissed the possibility of vertical migration of gases caused by overpressure. Overpressuring of a reservoir or aquifer will be necessary in order to have acceptable rates for dispersal of injected CO₂. This research describes methodology and the results of measurement of microseepage of CO₂ and CH₄ at a large-scale CO₂-enhanced oil recovery (EOR) operation at Rangely, Colorado, USA. Shallow and deep soil gas concentrations, and direct transport of CO₂ and CH₄ into the atmosphere were measured. The interpretation of the measurements was complemented by both stable and radiogenic isotopic measurements of C. The results have demonstrated an estimated microseepage to the atmosphere of approximately 400 metric tonnes of CH₄/a from the 78 km² area of the Rangely field. Preliminary estimates of deep-sourced CO₂ losses are <3800 tonnes/a, based on stable isotope measurements of soil gases. Several holes up to 10 m deep were drilled on, and off the field for nested gas sampling of composition and stable C isotopic ratios for CO₂ and CH₄. Carbon-14 measurements on CO₂ from these holes indicate that deep-sourced CO₂ microseepage losses were approximately 170 tonnes/a.     

中国农田的温室气体排放

中国是一个农业大国,拥有约1.33百万平方公里的农田。这些田地的种植、翻耕、施肥、灌溉等管理措施不仅长期改变着农田生态系统中的化学元素循环,而且给全球气候变化带来影响。农业生态系统对全球变化的影响主要是通过改变3种温室气体,即二氧化碳(CO₂)、甲烷(CH4)和氧化亚氮(N₂O)在土壤-大气界面的交换而实现的。为了分析多种因素(如气候、土壤质地、农作物品种及各种农田经营管理措施等)对农业土壤释放CO_22222222     

Globally increased pelagic carbonate production during the Mid-Brunhes dissolution interval and the CO2 paradox of MIS 11

The Mid-Brunhes dissolution interval (MBDI) represents a period of global carbonate dissolution, lasting several hundred thousand years, centred around Marine Isotope Stage (MIS) 11. Here we report the effects of dissolution in ODP core 982, taken from 1134 m in the North Atlantic. Paradoxically, records of atmospheric CO₂ from Antarctic ice-cores reveal no long term trend over the last 400 kyr and suggest that CO₂ during MIS 11 was no higher than during the present interglacial. We suggest that a global increase in pelagic carbonate production during this period, possibly related to the proliferation of the Gephyrocapsa coccolithophore, could have altered marine carbonate chemistry in such a way as to drive increased dissolution under the constraints of steady state. An increase in the production of carbonate in surface waters would cause a drawdown of global carbonate saturation and increase dissolution at the seafloor. In order to reconcile the record of atmospheric CO₂ variability we suggest that an increase in the flux of organic matter from the surface to deep ocean, associated with either a net increase in primary production or the enhanced ballasting effect provided by an increased flux of CaCO₃, could have countered the effect of increased calcification on CO₂.     

Site characterisation of a basin-scale CO<Subscript>2</Subscript> geological storage system: Gippsland Basin,southeast Australia

Geological storage of CO₂ in the offshore Gippsland Basin, Australia, is being investigated by the Cooperative Research Centre for Greenhouse Gas Technologies (CO2CRC) as a possible method for storing the very large volumes of CO₂ emissions from the nearby Latrobe Valley area. A storage capacity of about 50 million tonnes of CO₂ per annum for a 40-year injection period is required, which will necessitate several individual storage sites to be used both sequentially and simultaneously, but timed such that existing hydrocarbon assets will not be compromised. Detailed characterisation focussed on the Kingfish Field area as the first site to be potentially used, in the anticipation that this oil field will be depleted within the period 2015–2025. The potential injection targets are the interbedded sandstones of the Paleocene-Eocene upper Latrobe Group, regionally sealed by the Lakes Entrance Formation. The research identified several features to the offshore Gippsland Basin that make it particularly favourable for CO₂ storage. These include: a complex stratigraphic architecture that provides baffles which slow vertical migration and increase residual gas trapping and dissolution; non-reactive reservoir units that have high injectivity; a thin, suitably reactive, lower permeability marginal reservoir just below the regional seal providing mineral trapping; several depleted oil fields that provide storage capacity coupled with a transient production-induced flow regime that enhances containment; and long migration pathways beneath a competent regional seal. This study has shown that the Gippsland Basin has sufficient capacity to store very large volumes of CO₂. It may provide a solution to the problem of substantially reducing greenhouse gas emissions from future coal developments in the Latrobe Valley.     

Analysis of spatial distribution of global energy-related CO2 emissions

The purpose of this paper is to use the gravity theory to study the spatial distribution and centers of gravity for the global energy-related CO₂ emissions and to determine how they have changed over time. The main results are as follows: (1) In 2011, global energy-related CO₂ emissions reached 34,032.74 Mt, and Asia was the largest CO₂ emitter, which accounted for 45.25 % of total CO₂ emissions in the world. (2) Since 2006, China has exceeded the USA and become the biggest CO₂ emissions country. (3) In terms of the annual growth speed of CO₂ emissions, China is the fastest, followed by India, Saudi Arabia, Brazil, and South Africa. (4) During the study period, the center of gravity for CO₂ emissions is an overall movement toward the southeast, and Asia has become the center of gravity for CO₂ emissions.     

Carbon Dioxide and Methane Emissions from Mangrove-Associated Waters of the Andaman Islands,Bay of Bengal

We estimated CO₂ and CH₄ emissions from mangrove-associated waters of the Andaman Islands by sampling hourly over 24 h in two tidal mangrove creeks (Wright Myo; Kalighat) and during transects in contiguous shallow inshore waters, immediately following the northeast monsoons (dry season) and during the peak of the southwest monsoons (wet season) of 2005 and 2006. Tidal height correlated positively with dissolved O₂ and negatively with pCO₂, CH₄, total alkalinity (TAlk) and dissolved inorganic carbon (DIC), and pCO₂ and CH₄ were always highly supersaturated (330–1,627 % CO₂; 339–26,930 % CH₄). These data are consistent with a tidal pumping response to hydrostatic pressure change. There were no seasonal trends in dissolved CH₄ but pCO₂ was around twice as high during the 2005 wet season than at other times, in both the tidal surveys and the inshore transects. Fourfold higher turbidity during the wet season is consistent with elevated net benthic and/or water column heterotrophy via enhanced organic matter inputs from adjacent mangrove forest and/or the flushing of CO₂-enriched soil waters, which may explain these CO₂ data. TAlk/DIC relationships in the tidally pumped waters were most consistent with a diagenetic origin of CO₂ primarily via sulphate reduction, with additional inputs via aerobic respiration. A decrease with salinity for pCO₂, CH₄, TAlk and DIC during the inshore transects reflected offshore transport of tidally pumped waters. Estimated mean tidal creek emissions were ～23–173 mmol m^?2 day^?1 CO₂ and ～0.11–0.47 mmol m^?2 day^?1 CH₄. The CO₂ emissions are typical of mangrove-associated waters globally, while the CH₄ emissions fall at the low end of the published range. Scaling to the creek open water area (2,700 km²) gave total annual creek water emissions ～3.6–9.2?×?10¹⁰ mol CO₂ and 3.7–34?×?10⁷ mol CH₄. We estimated emissions from contiguous inshore waters at ～1.5?×?10¹¹ mol CO₂?year^?1 and 2.6?×?10⁸ mol CH₄?year^?1, giving total emissions of ～1.9?×?10¹¹ mol CO₂?year^?1 and ～3.0?×?10⁸ mol CH₄?year^?1 from a total area of mangrove-influenced water of ～3?×?10⁴ km². Evaluating such emissions in a range of mangrove environments is important to resolving the greenhouse gas balance of mangrove ecosystems globally. Future such studies should be integral to wider quantitative process studies of the mangrove carbon balance.     

Wood decomposition in Amazonian hydropower reservoirs: An additional source of greenhouse gases

Amazonian hydroelectric reservoirs produce abundant carbon dioxide and methane from large quantities of flooded biomass that decompose anaerobically underwater. Emissions are extreme the first years after impounding and progressively decrease with time. To date, only water-to-air fluxes have been considered in these estimates. Here, we investigate in two Amazonian reservoirs (Balbina and Petit Saut) the fate of above water standing dead trees, by combining a qualitative analysis of wood state and density through time and a quantitative analysis of the biomass initially flooded. Dead wood was much more decomposed in the Balbina reservoir 23 years after flooding than in the Petit Saut reservoir 10 years after flooding. Termites apparently played a major role in wood decomposition, occurring mainly above water, and resulting in a complete conversion of this carbon biomass into CO₂ and CH₄ at a timescale much shorter than reservoir operation. The analysis of pre-impounding wood biomass reveals that above-water decomposition in Amazonian reservoirs is a large, previously unrecognized source of carbon emissions to the atmosphere, representing 26–45% of the total reservoir flux integrated over 100 years. Accounting for both below- and above-water fluxes, we could estimate that each km² of Amazonian forest converted to reservoir would emit over 140 Gg CO₂-eq in 100 years. Hydropower plants in the Amazon should thus generate 0.25–0.4 MW h per km² flooded area to produce lower greenhouse gas emissions than gas power plants. They also have the disadvantage to emit most of their greenhouse gases the earliest years of operation.     

Life Cycle Assessment of Energy Balance and Emissions of a Wind Energy Plant

Life cycle analysis (LCA) methodology was used to perform a quantitative, comparative analysis and rating of the construction and operation of a wind energy plant. For this case study, the Glacier Hills Wind Park (90 1.8-MW turbines in south-central Wisconsin) was evaluated. Significant environmental and economic benefits are often advertised with the installation of new wind energy facilities, although independent and comprehensive LCA and sustainable energy science are typically not implemented. Hence, a quantitative demonstration with LCA methodology of the life cycle emissions and environmental impact, from construction through operations, can greatly assist in highlighting significant areas of energy consumption and emissions during manufacturing, transportation, and construction of a wind farm. Results portray the amount of greenhouse gas emissions and energy consumption/generation over the life cycle of the wind park. Transportation of large components from overseas led to the consumption of considerable quantities of fossil fuel, responsible for up to 22 % of the total greenhouse gas emissions due to transportation. The energy payback ratio (25.5), energy payback time (12.3 months) and the total grams of equivalent CO_2(eq) per kWh of energy (16.9) produced were calculated over the life time of this onshore wind farm.     

Using decomposition analysis to evaluate the performance of China’s 30 provinces in CO2 emission reductions over 2005–2009

This paper aims to evaluate the carbon dioxide (CO₂) emissions reduction performance of 30 mainland provinces in China over 2005?C2009. First, the log-mean Divisia index (LMDI) technique is used to decompose the changes in CO₂ emissions at the provincial level into 4 effects that are carbon intensity effect, energy mix effect, energy intensity effect and gross domestic product (GDP) effect. Next, two indicators, decoupling index and rescaled decoupling index, are implemented to evaluate the performance of 30 provinces in CO₂ emission reduction from 2005 to 2009. The decomposition result shows that the GDP growth is mainly responsible for the CO₂ emissions increase, while the energy intensity effect is the key factor for the decrease in CO₂ emissions in each province. Moreover, according to the evaluation, the performance of each province in what concerns the CO₂ emission reduction varies significantly. Most provinces in China made significant efforts in emissions reduction during 2005?C2009, while some provinces only made weak efforts or even no efforts in decoupling progress.     

Study on the CO<Subscript>2</Subscript> emissions embodied in the trade of China’s steel industry: based on the input–output model

The impact of trade on the environment and the climate has become a focus of attention. Tending to develop industries with higher added values, developed countries rely on importing high energy consumption goods from developing countries, and however, some CO₂ emissions are embodied in the process of import. Currently, the accounting method of the territorial responsibility used to get the international data of greenhouse gas inventories ignores the difference between domestic consumption and export demands. Thus, developing countries bear the responsibility of pollution emissions from the export. The steel industry is an important basic industry of China’s national economy as well as a vital part in the industrial system. With the expansion of trade scale, the impact of the export and import of China’s steel on CO₂ emissions is growing. This paper studied the embodied CO₂ emissions in the trade of China’s steel from 2005 to 2014, using the input–output model and the trade data of the China’s steel imports and exports. The results indicate that (1) the complete CO₂ emissions of China’s steel industry are high. (2) The increase in the export scale makes the embodied CO₂ emissions in the trade of China’s steel export increase, and (3) China is a net exporter of CO₂ emissions in the steel trade. Especially after 2007, the value of China’s steel exports has been larger than that of China’s steel imports, so China had borne much CO₂ emissions responsibility in the trade of China’s steel. Therefore, this paper puts forward that, in the future, the export structure of goods should be optimized into the high-tech products with the high added value, low energy consumption and low carbon emissions, and meanwhile, service industry is promoted to improve technical support to reduce CO₂ emissions in the steel industry.     

Simulation study of CO2 sequestration potential of the Mary Lee coal zone, Black Warrior basin

Significant potential exists for CO₂ sequestration in coalbed methane reservoirs of the Black Warrior basin. Reservoir simulation is an appropriate approach to estimate both the storage capacity and methane recovery enhancement. However, prior to a reliable reservoir modeling and simulation, conducting an accurate and comprehensive reservoir characterization study is necessary. The purpose of the present study is twofold: (a) to provide a rigorous reservoir characterization study required for modeling Mary Lee coal group in the Blue Creek field of the Black Warrior basin; (b) to run fluid flow simulations to predict the performance of ECBM process applied to an under pressured zone of the Mary Lee coal group. According to the current well configuration of Blue Creek field, three applicable well patterns, namely a direct line drive, an inverted 5-spot and a normal 5-spot were separately (i.e., in three distinct cases) used for simulating ECBM. Simulations were run on an approximately 32 ha (80-acre) drainage area, and included coal matrix shrinkage/swelling effects. The injected gas was assumed to be pure CO₂. Using an inverted 5-spot pattern, simulations predicted that after 7.5 years of CO₂ injection, approximately 32,000 tonnes of CO₂ would be sequestered per 32 ha of this zone and that methane recovery would be enhanced by 36 %. Using a normal 5-spot pattern, CO₂ breakthrough would occur 2.4 years earlier, and about 40,000 tonnes CO₂ would be sequestered. However, methane production would be enhanced by 33 %. Considering methane recovery enhancement, direct line drive pattern delivered poor results in comparison with two other patterns. As expected, the results also showed that CO₂ injection would increase water production.