Fluxes and pools of methane in wetland rice soils with varying organic inputs

Measurements of methane emission rates and concentrations in the soil were made during four growing seasons at the International Rice Research Institute in the Philippines, on plots receiving different levels of organic input. Fluxes were measured using the automated closed chambers system (total emission) and small chambers installed between plants (water surface flux). Concentrations of methane in the soil were measured by collecting soil cores including the gas phase (soil-entrapped methane) and by sampling soil solution in situ (dissolved methane). There was much variability between seasons, but total fluxes from plots receiving high organic inputs (16–24 g CH₄ m^–2) always exceeded those from the low input plots (3–9 g CH₄ m^–2). The fraction of the total emission emerging from the surface water (presumably dominated by ebullition) was greater during the first part of the season, and greater from the high organic input plots (35–62%) than from the low input plots (15–23%). Concentrations of dissolved and entrapped methane in the low organic input plots increased gradually throughout the season; in the high input plots there was an early-season peak which was also seen in emissions. On both treatments, periods of high methane concentrations in the soil coincided with high rates of water surface flux whereas low concentrations of methane were generally associated with low flux rates.     

Assessment of methane emission and oxidation at Air Hitam Landfill site cover soil in wet tropical climate

Methane (CH₄) emissions and oxidation were measured at the Air Hitam sanitary landfill in Malaysia and were modeled using the Intergovernmental Panel on Climate Change waste model to estimate the CH₄ generation rate constant, k. The emissions were measured at several locations using a fabricated static flux chamber. A combination of gas concentrations in soil profiles and surface CH₄ and carbon dioxide (CO₂) emissions at four monitoring locations were used to estimate the CH₄ oxidation capacity. The temporal variations in CH₄ and CO₂ emissions were also investigated in this study. Geospatial means using point kriging and inverse distance weight (IDW), as well as arithmetic and geometric means, were used to estimate total CH₄ emissions. The point kriging, IDW, and arithmetic means were almost identical and were two times higher than the geometric mean. The CH₄ emission geospatial means estimated using the kriging and IDW methods were 30.81 and 30.49 g m^?2 day^?1, respectively. The total CH₄ emissions from the studied area were 53.8 kg day^?1. The mean of the CH₄ oxidation capacity was 27.5 %. The estimated value of k is 0.138 year^?1. Special consideration must be given to the CH₄ oxidation in the wet tropical climate for enhancing CH₄ emission reduction.     

Empirical gas emission and oxidation measurement at cover soil of dumping site: example from Malaysia

Methane (CH₄) is one of the most relevant greenhouse gases and it has a global warming potential 25 times greater than that of carbon dioxide (CO₂), risking human health and the environment. Microbial CH₄ oxidation in landfill cover soils may constitute a means of controlling CH₄ emissions. The study was intended to quantify CH₄ and CO₂ emissions rates at the Sungai Sedu open dumping landfill during the dry season, characterize their spatial and temporal variations, and measure the CH₄ oxidation associated with the landfill cover soil using a homemade static flux chamber. Concentrations of the gases were analyzed by a Micro-GC CP-4900. Two methods, kriging values and inverse distance weighting (IDW), were found almost identical. The findings of the proposed method show that the ratio of CH₄ to CO₂ emissions was 25.4 %, indicating higher CO₂ emissions than CH₄ emissions. Also, the average CH₄ oxidation in the landfill cover soil was 52.5 %. The CH₄ and CO₂ emissions did not show fixed-pattern temporal variation based on daytime measurements. Statistically, a negative relationship was found between CH₄ emissions and oxidation (R ²?=?0.46). It can be concluded that the variation in the CH₄ oxidation was mainly attributed to the properties of the landfill cover soil.     

城市绿地温室气体通量监测与减排研究

采用LGR-密闭式动态通量箱法对城市绿地生态系统温室气体(CO₂、CH₄)通量的日变化、季节变化特征及其影响因子等进行了较为系统的研究。城市绿地花草CO₂通量有明显的日变化和季节变化特征,白天通量值为负,是CO₂的净吸收汇;夜晚为正值,是CO₂的净释放源;7:00左右由源转为汇,17:00左右由汇转为源,不同花卉24 h总通量有正负2种结果。冬季草坪作为源的时间延长,而作为汇的时间缩短。光强和温度是影响CO₂通量日变化和季节变化的主要因素。城市绿地CH₄通量较小,不足以对温室气体总量产生显著影响。从减少温室气体排放的角度对城市绿地花草的选择提出了建议。     

Air Pollution and Heat Exposure Study in the Workplace in a Glass Manufacturing Unit in India

Air pollution in the workplace environment due to industrial operation have been found to cause serious occupational health hazard. Similarly, heat stress is still most neglected occupational hazard in the tropical and subtropical countries like India. The hot climate augments the heat exposure close to sources like furnaces. In this study an attempt is made to assess air pollution and heat exposure levels to workers in the workplace environment in glass manufacturing unit located in the State of Gujarat, India. Samples for workplace air quality were collected for SPM, SO₂, NO₂ and CO₂ at eight locations. Results of workplace air quality showed 8-hourly average concentrations of SPM: 165–9118 μg/m³, SO₂: 6–9 μg/m³ and NO₂: 5–42 μg/m³, which were below the threshold limit values of workplace environment. The level of CO₂ in workplace air of the plant was found to be in the range 827–2886 μg/m³, which was below TLV but much higher than the normal concentration for CO₂ in the air (585 mg/m³). Indoor heat exposure was studied near the furnace and at various locations in an industrial complex for glass manufacturing. The heat exposure parameters including the air temperature, the wet bulb temperature, and the globe parameters were measured. The Wet Bulb Globe Temperature (WBGT), an indicator of heat, exceeded ACGIH TLVs limits most of the time at all the locations in workplace areas. The recommended duration of work and rest have also been estimated.     

Hydrogeochemical characterization of contaminated groundwater in Patancheru industrial area,southern India

The groundwater is one of the most contaminated natural resources in Patancheru industrial area due to unplanned and haphazard industrial growth and urbanization without following basic pollution control norms. The rapid industrialization initiated in early 1970 has started showing up its after effects few years later in the form of physiochemical contamination of the both surface and groundwater bodies of the area. It has resulted in local people being deprived of safe drinking water, plant and aquatic life has severely affected, and situation is deteriorating over the years in the area in spite of some preventive and remedial measures being initiated. The focus of the present study is to understand the chemical characteristics of groundwater and geochemical processes the contaminant water is undergoing which are normally imprinted in its ionic assemblages. The water samples collected in pre- and post-monsoon seasons from forty two groundwater and four surface water sources were analyzed for major constituents such as Ca²⁺, Mg²⁺, Na⁺, K⁺, CO₃⁻, HCO₃⁻, Cl⁻, SO₄²⁻, NO₃⁻, and F⁻, and selected samples were tested for ten important trace metals like Fe, Pb, Bi, Mn, Cr, Co, Ni, Cu, Zn, and Cd. Na⁺ among cations and Cl⁻ among anions dominate the water in both the seasons where as Ca²⁺, HCO₃⁻, and Cl⁻ show significant reduction in their ionic strength in post-monsoon. The groundwater in general is of mixed type, but most of it belong to Na⁺–Cl⁻, Na⁺–HCO₃⁻, Ca²⁺–Mg²⁺–HCO₃⁻, and Ca²⁺–Mg²⁺–Cl⁻ facies. The Na⁺ and Ca²⁺ are in the transitional state with Na⁺ replacing Ca²⁺ and HCO₃⁻–Cl⁻ due to physiochemical changes in the aquifer system. The evaluation of hydrochemistry through various ionic indices, ratios, and plots suggest that silicate–carbonate weathering, ion exchange, dissolution, and evaporation processes are responsible for origin of the present chemical status of the groundwater which is also controlled by the contamination from extraneous sources that could have accelerated the dissolution processes. Gibbs plots authenticate that the evolution of water chemistry is influenced by interaction of percolating water with aquifer matrix apart from anthropogenic enrichment of elements which get over concentrated due to evaporation.     

华东森林及高山背景区域CO2和CH4浓度变化特征

对国家大气背景监测福建武夷山站2014—2018年的主要温室气体监测数据进行分析,探讨华东森林及高山背景区域大气中CO_2和CH_4浓度的变化特征。结果表明:华东森林及高山区域CO_2背景浓度为414.1×10~(-6)(摩尔分数,下同),5年间呈逐年上升趋势; CH_4背景浓度为1 977×10~(-9),2014—2016年呈逐年上升趋势,2016—2018年保持稳定;两者均具有较明显的季节和月变化特征,CO_2还具有较明显的日变化特征,但季节变化幅度、月平均浓度振幅和日变化幅度均较小,具有区域背景特征。     

The effect of atmospheric pressure on CH4 and CO2 emission from a closed landfill site in Manchester, UK

A time series study was conducted to ascertain the effect of barometric pressure on the variability of CH₄ and CO₂ concentrations in a closed landfill site. An in situ data of methane/carbon dioxide concentrations and environmental parameters were collected by means of an in-borehole gas monitor, the GasClam (Ion Science, UK). Linear regression analysis was used to determine the strength of the correlation between ground-gas concentrations and barometric pressure. The result shows CH₄ and CO₂ concentrations to be variable with weak negative correlations of 0.2691 and 0.2773, respectively, with barometric pressure over the entire monitoring period. Although the R ² was slightly improved by considering their concentration over single periods of rising and falling pressure, single periods of rising pressure and single periods of falling pressure, their correlations remained insignificant at 95 % confidence level. The result revealed that atmospheric pressure—the acclaimed major control on the variability of ground-gas concentration—is not always so. A case was made for the determination of other possible controls such as changes in temperature, soil permeability, landfill water depth, season, and geology of the borehole and also how much of control each factor would have on the variability/migration of CH₄ and CO₂ concentrations from the studied landfill.     

Gastro-enteric methane versus sulphate and volatile fatty acid production

The breakdown of low digestible components present in food during passage through the human and animal gastro-intestinal (GI) tract is performed by the highly diverse microbial community present in this ecosystem. Fermentation of these substances yields, besides CO₂ and volatile fatty acids, H₂, which is used as a substrate by three different H₂-consuming bacteria. Sulphate-reducing bacteria (SRB) use H₂ to reduce SO _inf4 ^sup2- to H₂S, hydrogenotrophic methane-producing bacteria (MPB) use H₂ to reduce CO₂ to CH₄ and reductive acetogens (RAC) use H₂ to reduce CO₂ to CH₃COOH. A competition between these three bacterial groups exists for the common H₂ substrate. This results generally in the dominance of one group above the other two.     

Carbon dioxide flux across a forest-field ecotone

CO₂ flux of a deciduous forest and an old-field surface, and the ecotone between these two typical southern U.S. ecological communities, was studied in July, 1989. Rates of CO₂ flux were greatest in the old field and least in the forest plots. The ecotone showed the greatest variation in CO₂ flux. These differences appear to be due to differences in soil surface temperature, the old field being more exposed to direct solar radiation. The ecotonal community represents a landscape property which should be considered in studies of the transfer of carbon across the soil-atmosphere boundary.     

Long-term spatiotemporal patterns of CH4 and N2O emissions from livestock and poultry production in Turkey

This study quantified spatiotemporal patterns of CH₄ and N₂O emissions from livestock and poultry production in Turkey between 1961 and 2007. CH_4(enteric) (from enteric fermentation), CH_4(manure) (from manure management), and N₂O_(AWM) (from animal waste management) emissions in Turkey were estimated at 1,164, 216, and 55 Gg in 1961 and decreased to 844, 187, and 39 Gg in 2007, contributing a share of roughly 2% to the global livestock-related CH₄ emissions and %1.5 to the global N₂O_(AWM) emissions, respectively. Total CO₂-eq emissions were estimated at 50.7 Tg in 1961 and declined from a maximum value of 60.7 Tg in 1982 to a minimum value of 34.5 Tg in 2003, with a mean emission rate of 48 Tg year^???1 due to a significant reduction in the number of ruminant livestock. The highest mean share of emissions belonged to West Black Sea (14% and 16%) for CH_4(enteric) and CH_4(manure) and to North East Anatolia (12% and %13) for N₂O_(AWM) and total CO₂-eq emissions, respectively. The highest emission density was 1.7 Mg km^???2 year^???1 for CH_4(enteric), 0.3 Mg km^???2 year^???1 for CH_4(manure), and 0.07 Mg km^???2 year^???1 for the total CO₂-eq emissions in the West and North East Anatolia regions and 0.09 Mg km^???2 year^???1 for N₂O_(AWM) in the East Marmara region. Temporal and spatial variations in CH_4(enteric), CH_4(manure), and N₂O_(AWM) emissions in Turkey were estimated using regression models and ordinary kriging at a 500-m resolution, respectively.     

Spatio-temporal variations of carbon dioxide and its gross emission regulated by artificial operation in a typical hydropower reservoir in China

Supersaturation and excess emission of greenhouse gases in freshwater reservoirs have received a great deal of attention in recent years. Although impoundment of reservoirs has been shown to contribute to the net emission of greenhouse gases, reservoir age, geographical distribution, submerged soil type and artificial regulation also have a great impact on their emissions. To examine how large scale reservoir operation impact the water column CO₂ and its air–water interface flux, a field study was conducted in 2010 to evaluate potential ecological processes that regulate the partial pressure of CO₂ (pCO₂) in the water column in the Pengxi River backwater area (PBA), a typical tributary in the Three Gorges Reservoir, China. Measurements of total alkalinity (TA), pH and water temperature were applied to compute the pCO₂. And this approach was also validated by calculation of pCO₂ from the dissolved inorganic carbon data of samples. Partial least squares (PLS) regression was used to determine how the dynamics of the water pCO₂ were related to the available variables. The estimated pCO₂ in our sample ranged from 26 to 4,087 μatm in the surface water. During low water operation from July to early September, there was an obvious pCO₂ stratification, and pCO₂ in the surface was almost unsaturated. This phenomenon was also observed in the spring bloom during discharge period. Conversely, there was no significant pCO₂ stratification and the entire water column was supersaturated during high water operation from November to the following February. Significant correlation was observed between the magnitude of pCO₂, DO and chlorophyll a, suggesting that phytoplankton dynamics regulate pCO₂ in the PBA. The average areal rate of CO₂ emissions from the Pengxi River ranged from 18.06 to 48.09 mmol m^?2 day^?1, with an estimated gross CO₂ emission from the water surface of 14–37 t day^?1 in this area in 2010. Photosynthesis and respiration rates by phytoplankton might be the dominant processes that regulated pCO₂ in the water column. We conclude that pCO₂ values in the surface water of Pengxi River could be regarded as potential sources of CO₂ to the atmosphere were smaller or similar to those that have been reported for many other reservoirs to date.     

Implications of climate change for evaporation from bare soils in a Mediterranean environment

The purpose of this study was to predict quantitative changes in evaporation from bare soils in the Mediterranean climate region of Turkey in response to the projections of a regional climate model developed in Japan (hereafter RCM). Daily RCM data for the estimation of reference evapotranspiration (ET _r) and soil evaporation were obtained for the periods of 1994–2003 and 2070–2079. Potential evaporation (E _p) from bare soils was calculated using the Penman–Monteith equation with a surface resistance of zero. Simulation of actual soil evaporation (E _a) was carried out using Aydin model (Aydin et al., Ecological Modelling 182:91–105, 2005) combined with Aydin and Uygur (2006, A model for estimating soil water potential of bare fields. In Proceedings of the 18th International Soil Meeting (ISM) on Soils Sustaining Life on Earth, Managing Soil and Technology, Sanliurfa, 477–480pp.) model of predicting soil water potential at the top surface layer of a bare soil, after performances of Aydin model (R ² = 94.0%) and Aydin and Uygur model (R ² = 97.6) were tested. The latter model is based on the relations among potential soil evaporation, hydraulic diffusivity, and soil wetness, with some simplified assumptions. Input parameters of the model are simple and easily obtainable such as climatic parameters used to compute the potential soil evaporation, average diffusivity for the drying soil, and volumetric water content at field capacity. The combination of Aydin and Aydin and Uygur models appeared to be useful in estimating water potential of soils and E _a from bare soils, with only a few parameters. Unlike ET _r and E _p projected to increase by 92 and 69 mm (equivalent to 8.0 and 7.3% increases) due to the elevated evaporative demand of the atmosphere, respectively, E _a from bare soils is projected to reduce by 50 mm (equivalent to a 16.5% decrease) in response to a decrease in rainfall by 46% in the Mediterranean region of Turkey by the 2070s predicted by RCM, and consequently, to decreased soil wetness in the future.     

CH4 and CO emissions from rice straw burning in South East Asia

Atmospheric samples collected during rice straw burning at four different locations in Viet-Nam during the dry (March 1992, February 1993) and wet season (August 1992) were analysed for CO₂, CO, and CH₄. The emission ratios relative to CO₂ for CO and CH₄ for rice straw burning during the dry season were comparable to those observed on samples collected during burning of savanna in Africa or forest in the USA. During the wet season, however the emission ratios for CO and CH₄ relative to CO₂ were 3 to 10 times higher. With these emission ratios and estimates of rice production from Southeastern Asia, we estimated that burning of rice straw emits annually about 2.2 Tmol of CO (26 TgC) and 0.2 Tmol of CH₄ (2.4 TgC) to the atmosphere. Taking into account these new results, CO and CH₄ fluxes from biomass burning could be reevaluated by 5–21% and 5–24%, respectively, in respect with previous estimates of these gas emissions from all biomass burning activities.     

Major ion chemistry of shallow groundwater of a fast growing city of Central India

Nagpur City located in semiarid area of central India is a fast-growing industrial centre. In recent years, rapid development has created an increased demand for drinking water, which is increasingly being fulfilled by groundwater abstraction. The present study was undertaken to assess major ion chemistry of shallow groundwater to understand geochemical evolution of groundwater and water quality for promoting sustainable development and effective management of groundwater resources. A total of 47 water samples were collected from shallow aquifer of selected parts of the city and the water chemistry of various ions viz. Ca^2 +, Mg^2 +, Na⁺, K⁺, CO₃  ^2-_{3}^{\ \, 2-}, HCO₃  ^-_{3}^{\ \, -}, Cl⁻, SO₄  ^2-_{4}^{\ \,2-} and NO₃  ^-_{3}^{\ \,-} are carried out. The chemical relationships in Piper diagram identify Ca–HCO₃–Cl and mixed Ca–Na–HCO₃–Cl as most prevalent water types. Alkaline earth exceeds alkalis and weak acids exceed strong acids. Ionic ratios and Gibb’s diagram suggest that silicate rock weathering and anthropogenic activities are the main processes that determine the ionic composition in the study area. The nitrate appeared as a major problem of safe drinking water in this region. We recorded highest nitrate concentration, i.e., 411 mg/l in one of the dug well. A comparison of groundwater quality in relation to drinking water quality standards revealed that about half of the shallow aquifer samples are not suitable for drinking.     

Identifying the European Fossil Fuel Plumes in the Atmosphere Over the Northeast Atlantic Region Through Isotopic Observations and Numerical Modelling

As part of the Danish NEAREX project the origin and variability of anthropogenic atmospheric CO₂ over the Northeast Atlantic Region (NEAR) has been studied. The project consisted of a combination of experimental and modelling activities. Local volunteers operated CO₂ sampling stations, built at University of Copenhagen, for ¹⁴C analysis at four locations (East Denmark, Shetland Isles, Faroe Isles and Iceland). The samples were only collected during winter periods of south-easterly winds in an attempt to trace air enriched in fossil-fuel derived CO₂ due to combustion of fossil fuels within European countries. In order to study the transport and concentration fields over the region in detail, a three-dimensional Eulerian hemispheric air pollution model has been extended to include the main anthropogenic sources for atmospheric CO₂. During the project period (1998–2001) only a few episodes of transport from Central Europe towards NEAR arose, which makes the data set for the evaluation of the method sparse. The analysed samples indicate that the signal for fossil CO₂, as expected, is largest (up to 3.7±0.4% fossil CO₂) at the Danish location closest to the European emissions areas and much weaker (up to ∼1.5±0.6% fossil CO₂) at the most remote location. As the anthropogenic signal is weak in the clean atmosphere over NEAR these numbers will, however, be very sensitive to the assumed background ¹⁴CO₂ activity and the precision of the measurements. The model simulations include the interplay between the driving processes from the emission into the boundary layer and the following horizontal/vertical mixing and atmospheric transport and are used to analyse the meteorological conditions leading to the observed events of high fossil CO₂ over NEAR. This information about the history of the air masses is essential if an observed signal is to be utilised for identifying and quantifying sources for fossil CO₂.     

Water pollution in relation to mineral exploration: a case study from Alayi-Ovim area of Southeastern Nigeria

Water samples from rivers, streams, springs, and shallow wells in Alayi-Ovim area of southeast Nigeria have been analyzed for Pb, Ca, Mg, Fe, Mg, PO₄, NO₃, CO₃, SO₄, Cl, and pH. The analyses were carried out using atomic absorption spectrometer and Hach Direct Reading Equipment. Results of the analyses from the area conform to the WHO (1995) standards for drinking water. However, the results show relative enrichment of Ca, pH, Mg, CO₃, and Cl. Low values were obtained for Fe, SO₄, and NO₃. While the Cl and Pb enrichment in the area north of Alayi-Ovim axis is attributed to proximity to the lead–zinc and chloride-rich formations of the Turonian Eze-Aku and the Albian Asu River; the Ca, Mg, SO₄, and CO₃ enrichment in Southern part of Alayi-Ovim is due to the limestone-bearing Late Maastrichtian Nsukka Formation. Furthermore, the very low values of less than 5 ppm for these characters in water in the central region correlate well with the relatively clean Maastrichtian quartz arenite Ajali Sandstone Formation. The Pb–Zn and Cl incursions into the water system from the Older Albian Asu River/Turonian Eze-Aku Formations in the northern part of Alayi-Ovim area and the leaching of Mg, and Ca into the water system in the Maastrichtian limestone area in the south thus constitute geochemical indices for chemical pollution and mineral exploration for brine and dolomitic limestone in the area.     

Inspection of non-CO2 greenhouse gases from emission sources and in ambient air by Fourier-transform-infrared-spectrometry: Measurements with FTIS-MAPS

Infrared spectrometry is a versatile basis to analyse greenhouse gases in the atmosphere. A multicomponent air pollution software (MAPS) was developed for retrieval of gas concentrations from radiation emission as well as absorption measurements. Concentrations of CO, CH₄, N₂O, and H₂O as well as CO₂, NO, NO₂, NH₃, SO₂, HCl, HCHO, and the temperature of warm gases are determined on-line. The analyses of greenhouse gases in gaseous emission sources and in ambient air are performed by a mobile remote sensing system using the double-pendulum interferometer K300 of the Munich company Kayser-Threde. Passive radiation measurements are performed to retrieve CO, N₂O, and H₂O as well as CO₂, NO, SO₂, and HCl concentrations in smoke stack effluents of thermal power plants and municipal incinerators and CO and H₂O as well as CO₂ and NO in exhausts of aircraft engines. Open-path radiation measurements are used to determine greenhouse gas concentrations at different ambient air conditions and greenhouse gas emission rates of diffusive sources as garbage deposits, open coal mining, stock farming together with additional compounds (e.g. NH₃), and from road traffic together with HCHO. Some results of measurements are shown. A future task is the verification of emission cadastres by these inspection measurements.     

Transport and Adhesion of Escherichia coli JM109 in Soil Aquifer Treatment (SAT): One-Dimensional Column Study

Bacteria transport and adhesion experiments under water-saturated and partially saturated conditions were examined over a wide range of ionic strength, from 1 to 100 mM KCl, CaCl₂, and MgCl₂, and at water contents of 0.15 and 0.22 in sand columns packed with three different sands, baked, sterilized, and raw sands in order to investigate the effects of ionic strength, water content, and porous media type on the microbial adhesion in soil aquifer treatment (SAT). Well-characterized Escherichia coli JM109 were used as model bacterial cells in this study. Column study results showed that bacterial deposition rates increased with increasing ionic strength and decreasing water content, and were higher in raw sand columns than those in other sand columns. The Derjaguin–Landau–Verwey–Overbeek (DLVO) theory was applied to experimental results in order to consider the interaction energies between the bacterial cells and collector grains; results revealed that a considerable amount of bacterial cells was weakly deposited onto the solid surfaces in secondary minimum.     

CO2 Capture and Storage with Leakage in an Energy-Climate Model

Geological CO₂ capture and storage (CCS) is among the main near-term contenders for addressing the problem of global climate change. Even in a baseline scenario, with no comprehensive international climate policy, a moderate level of CCS technology is expected to be deployed, given the economic benefits associated with enhanced oil and gas recovery. With stringent climate change control, CCS technologies will probably be installed on an industrial scale. Geologically stored CO₂, however, may leak back to the atmosphere, which could render CCS ineffective as climate change reduction option. This article presents a long-term energy scenario study for Europe, in which we assess the significance for climate policy making of leakage of CO₂ artificially stored in underground geological formations. A detailed sensitivity analysis is performed for the CO₂ leakage rate with the bottom-up energy systems model MARKAL, enriched for this purpose with a large set of CO₂ capture technologies (in the power sector, industry, and for the production of hydrogen) and storage options (among which enhanced oil and gas recovery, enhanced coal bed methane recovery, depleted fossil fuel fields, and aquifers). Through a series of model runs, we confirm that a leakage rate of 0.1%/year seems acceptable for CCS to constitute a meaningful climate change mitigation option, whereas one of 1%/year is not. CCS is essentially no option to achieve CO₂ emission reductions when the leakage rate is as high as 1%/year, so more reductions need to be achieved through the use of renewables or nuclear power, or in sectors like industry and transport. We calculate that under strict climate control policy, the cumulative captured and geologically stored CO₂ by 2100 in the electricity sector, when the leakage rate is 0.1%/year, amounts to about 45,000 MtCO₂. Only a little over 10,000 MtCO₂ cumulative power-generation-related emissions are captured and stored underground by the end of the century when the leakage rate is 1%/year. Overall marginal CO₂ abatement costs increase from a few €/tCO₂ today to well over 150 €/tCO₂ in 2100, under an atmospheric CO₂ concentration constraint of 550 ppmv. Carbon costs in 2100 turn out to be about 40 €/tCO₂ higher when the annual leakage rate is 1%/year in comparison to when there is no CO₂ leakage. Irrespective of whether CCS deployment is affected by gradual CO₂ seepage, the annual welfare loss in Europe induced by the implementation of policies preventing “dangerous anthropogenic interference with the climate system” (under our assumption, implying a climate stabilisation target of 550 ppmv CO₂ concentration) remains below 0.5% of GDP during the entire century.