Variations in dissolved CO2 and CH4 in a first‐order stream and catchment: an investigation of soil–stream linkages

Spatial and seasonal variations in CO₂ and CH₄ concentrations in streamwater and adjacent soils were studied at three sites on Brocky Burn, a headwater stream draining a peatland catchment in upland Britain. Concentrations of both gases in the soil atmosphere were significantly higher in peat and riparian soils than in mineral soils. Peat and riparian soil CO₂ concentrations varied seasonally, showing a positive correlation with air and soil temperature. Streamwater CO₂ concentrations at the upper sampling site, which mostly drained deep peats, varied from 2·8 to 9·8 mg l^?1 (2·5 to 11·9 times atmospheric saturation) and decreased markedly downstream. Temperature‐related seasonal variations in peat and riparian soil CO₂ were reflected in the stream at the upper site, where 77% of biweekly variation was explained by an autoregressive model based on: (i) a negative log‐linear relationship with stream flow; (ii) a positive linear relationship with soil CO₂ concentrations in the shallow riparian wells; and (iii) a negative linear relationship with soil CO₂ concentrations in the shallow peat wells, with a significant 2‐week lag term. These relationships changed markedly downstream, with an apparent decrease in the soil–stream linkage and a switch to a positive relationship between stream flow and stream CO₂. Streamwater CH₄ concentrations also declined sharply downstream, but were much lower (<0·01 to 0·12 mg l^?1) than those of CO₂ and showed no seasonal variation, nor any relationship with soil atmospheric CH₄ concentrations. However, stream CH₄ was significantly correlated with stream flow at the upper site, which explained 57% of biweekly variations in dissolved concentrations. We conclude that stream CO₂ can be a useful integrative measure of whole catchment respiration, but only at sites where the soil–stream linkage is strong. Copyright © 2004 John Wiley & Sons, Ltd.     

城市湖泊不同水生植被区水体温室气体溶存浓度及其影响因素

为了解城市湖泊不同水生植被区水体温室气体的溶存浓度及其影响因素,于2015年4-11月按每月2次的频率采用顶空平衡法对聊城市铃铛湖典型植被区——菹草区、莲藕区和睡莲区表层水中CO₂、CH₄和N₂O的溶存浓度进行监测,计算水中温室气体的饱和度和排放通量,并测定水温（T）、pH、溶解氧（DO）、叶绿素a及营养盐浓度等理化指标,以探究水体环境因子对温室气体溶存浓度的影响.结果表明,铃铛湖各植被区水体温室气体均处于过饱和状态,是大气温室气体的"源";莲藕区CH₄浓度、饱和度和排放通量均显著高于菹草区,而各植被区N₂O和CO₂均无显著性差异;不同植被区湖水中DO、总氮（TN）、总磷（TP）和硝态氮（NO₃^--N）浓度具有显著差异,其中DO、TN和NO₃^--N浓度均表现为菹草区最高,莲藕区最低,而TP浓度则正好相反;各植被区温室气体浓度和水环境参数间的相关分析和多元回归分析的结果表明,水生植物可通过影响水体的理化性质对温室气体的产生和排放产生显著差异影响,在菹草区亚硝态氮（NO₂^--N）、NO₃^--N、T和DO是控制水体温室气体浓度的主要因子;睡莲区为TP和pH;莲藕区则为pH、NO₂^--N和DO.     

The impact of pipe flow in riparian peat deposits on nitrate transport and removal

The effect of preferential flow in soil pipes on nitrate retention in riparian zones is poorly understood. The characteristics of soil pipes and their influence on patterns of groundwater transport and nitrate dynamics were studied along four transects in a 1‐ to >3‐m deep layer of peat and marl overlying an oxic sand aquifer in a riparian zone in southern Ontario, Canada. The peat‐marl deposit, which consisted of several horizontal layers with large differences in bulk density, contained soil pipes that were generally 0.1 to 0.2 m in diameter and often extended vertically for 1 to >2 m. Springs that produced overland flow across the riparian area occurred at some sites where pipes extended to the peat surface. Concentrations of NO₃^?–N (20–30 mg L^?1) and dissolved oxygen (DO) (4–6 mg L^?1) observed in peat pipe systems and surface springs were similar to values in the underlying sand aquifer, indicating that preferential flow transported groundwater with limited nitrate depletion. Low NO₃^?–N concentrations of <5 mg L^?1 and enriched δ¹⁵N values indicated that denitrification was restricted to small areas of the peat where pipes were absent. Groundwater DO concentrations declined rapidly to <2 mg L^?1 in the peat matrix adjacent to pipes, whereas high NO₃^?–N concentrations of >15 mg L^?1 extended over a larger zone. Low dissolved organic carbon values at these locations suggest that supplies of organic carbon were not sufficient to support high rates of denitrification, despite low DO conditions. These data indicate that it is important to develop a greater understanding of pipes in peat deposits, which function as sites where the transport of large fluxes of water with low biogeochemical reaction rates can limit the nitrate removal capacity of riparian zones. Copyright © 2011 John Wiley & Sons, Ltd.     

Photochemistry of Ions at D-region Altitudes of the Ionosphere: A Review

The current state of knowledge of the D-region ion photochemistry is reviewed. Equations determining production rates of electrons and positive ions by photoionization of atmospheric neutral species are presented and briefly discussed. Considerable attention is given to the progress in the chemistry of O⁺(⁴S), O⁺(²D), O⁺(²P), N⁺, N₂ ⁺, O₂ ⁺, NO⁺, N₄ ⁺, O₄ ⁺, NO⁺(N₂), NO⁺(CO₂), NO⁺(CO₂)₂, NO⁺(H₂O) _n for n = 1–3, NO⁺(H₂O)(N₂), NO⁺(H₂O)₂(N₂), NO⁺(H₂O)(CO₂), NO⁺(H₂O)₂(CO₂), O₂ ⁺(H₂O), H₃O⁺(OH), H⁺(H₂O) _n for n = 1–8, O^?, O₂ ^?, O₃ ^?, O₄ ^?, OH^?, CO₃ ^?, CO₄ ^?, NO₂ ^?, NO₃ ^?, ONOO^?, Cl^?, Cl^?(H₂O), Cl^?(CO₂), HCO₃ ^?, CO₃ ^?(H₂O), CO₃ ^?(H₂O)₂, NO₃ ^?(H₂O), NO₃ ^?(H₂O)₂, OH^?(H₂O), and OH^?(H₂O)₂ ions. The analysis of the D-region rocket ion mass spectrometer measurements shows that, among these ions, O₂ ⁺, NO⁺, NO⁺(H₂O), and H⁺(H₂O) _n for n = 1–7 can make the main contribution to the total positive ion number density, and O^?, O₂ ^?, Cl^?, OH^?(H₂O), CO₃ ^?, HCO₃ ^?, NO₃ ^?, ONOO^?, CO₄ ^?, NO₃ ^?(H₂O), NO₃ ^?(H₂O)₂, and ³⁵Cl^?(CO₂) ions can be responsible for the main contribution to the total negative ion number density. Photodetachment of electrons from O^?, Cl^?, O₂ ^?, O₃ ^?, OH^?, NO₂ ^?, and NO₃ ^?, dissociative electron photodetachment of O₄ ^? and OH^?(H₂O), and photodissociation of O₃ ^?, O₄ ^?, CO₃ ^?, CO₄ ^?, ONOO^?, HCO₃ ^?, CO₃ ^?(H₂O), NO₃ ^?(H₂O), O₂ ⁺(H₂O), O₄ ⁺, N₄ ⁺, NO⁺(H₂O), NO⁺(H₂O)₂, H⁺(H₂O) _n for n = 2–4, NO⁺(N₂), and NO⁺(CO₂) are studied, and the photodetachment and photodissociation rate coefficients are calculated using the current state of knowledge on the cross sections of these processes and fluxes of solar radiation.     

The fluvial flux of particulate organic matter from the UK: the emission factor of soil erosion

Soil erosion has been identified as a potential global carbon sink since eroded organic matter is replaced at source and eroded material is readily buried. However, this argument has relied on poor estimates of the total fate of in‐transit particulates and could erroneously imply soil erosion could be encouraged to generate carbon stores. These previous estimates have not considered that organic matter can also be released to the atmosphere as a range of greenhouse gases, not only carbon dioxide (CO₂), but also the more powerful greenhouse gases methane (CH₄) and nitrous oxide (N₂O). As soil carbon lost by erosion is only replaced by uptake of CO₂, this could represent a considerable imbalance in greenhouse gas warming potential, even if it is not significant in terms of overall carbon flux. This work therefore considers the flux of particulate organic matter through UK rivers with respect to both carbon fluxes and greenhouse gas emissions. The results show that, although emissions to the atmosphere are dominated by CO₂, there are also considerable fluxes of CH₄ and N₂O. The results suggest that soil erosion is a net source of greenhouse gases with median emission factors of 5.5, 4.4 and 0.3 tonnes CO_2eq/yr for one tonne of fluvial carbon, gross carbon erosion and gross soil erosion, respectively. This study concludes that gross soil erosion would therefore only be a net sink of both carbon and greenhouse gases if all the following criteria are met: the gross soil erosion rate were very low (<91 tonnes/km²/yr); the eroded carbon were completely replaced by new soil organic matter; and if less than half of the gross erosion made it into the stream network. By establishing the emission factor for soil erosion, it becomes possible to properly account for the benefits of good soil management in minimizing losses of greenhouse gases to the atmosphere as a by‐product of soil erosion. Copyright © 2015 John Wiley & Sons, Ltd.     

Transfer of carbon dioxide and methane through the soil‐water‐atmosphere system at Mer Bleue peatland,Canada

Surface waters associated with peatlands, supersaturated with CO₂ and CH₄ with respect to the atmosphere, act as important pathways linking a large and potentially unstable global repository of C to the atmosphere. Understanding the drivers and mechanisms which control C release from peatland systems to the atmosphere will contribute to better management and modelling of terrestrial C pools. We used non‐dispersive infra‐red (NDIR) CO₂ sensors to continuously measure gas concentrations in a beaver pond at Mer Bleue peatland (Canada); measurements were made between July and August 2007. Concentrations of CO₂ in the surface water (10 cm) reached 13 mg C l^?1 (epCO₂ 72), and 26 mg C l^?1 (epCO₂ 133) at depth (60 cm). The study also showed large diurnal fluctuations in dissolved CO₂ which ranged in amplitude from ～1·6 mg C l^?1 at 10 cm to ～0·2 mg C l^?1 at 60 cm depth. CH₄ concentration and supersaturation (epCH₄) measured using headspace analysis averaged 1·47 mg C l^?1 and 3252, respectively; diurnal cycling was also evident in CH₄ concentrations. Mean estimated evasion rates of CO₂ and CH₄ over the summer period were 44·92 ± 7·86 and 0·44 ± 0·25 µg C m^?2s^?1, respectively. Open water at Mer Bleue is a significant summer hotspot for greenhouse gas emissions within the catchment. Our results suggest that CO₂ concentrations during the summer in beaver ponds at Mer Bleue are strongly influenced by biological processes within the water column involving aquatic plants and algae (in situ photosynthesis and respiration). In terms of carbon cycling, soil‐stream connectivity at this time of year is therefore relatively weak. Copyright © 2008 John Wiley & Sons, Ltd.     

三峡水库澎溪河消落区土-气界面CO2和CH4通量初探

水库近岸湿地(消落区)温室气体(CO₂、CH₄)产汇是水库温室气体效应问题的重要组成部分.本文以三峡水库支流澎溪河的白家溪、养鹿两处大面积消落区为研究对象,于2010年6 9月水库低水位运行期间,对近岸消落区土-气界面CO₂、CH₄通量进行监测.白家溪消落区土-气界面CO₂通量均值为12.38±2.42 mmol/(m²·h);CH₄通量均值为0.0112±0.0064 mmol/(m²·h).养鹿消落区CO₂、CH₄通量均值分别为10.54±5.17、0.14±0.16 mmol/(m²·h).总体上,6 9月土-气界面CO₂通量呈增加趋势,而CH₄通量水平呈现显著的递减趋势.消落区土地出露后植被恢复,在一定程度上促进了土壤有机质含量的增加,使得6 9月CO₂释放通量的总体趋势有所增加.消落区退耕后,其甲烷氧化菌的活性得到恢复,加之在土地出露曝晒过程中土壤透气性增强,使得消落区土壤对大气中CH₄吸收氧化潜势增强.尽管如此,仍需进一步的研究以明晰消落区土-气界面CO₂、CH₄产汇的主要影响因素.     

Beaver dams along an agricultural stream in southern Ontario,Canada: their impact on riparian zone hydrology and nitrogen chemistry

The hydrology and nitrogen biogeochemistry of a riparian zone were compared before and after the construction of beaver dams along an agricultural stream in southern Ontario, Canada. The beaver dams increased surface flooding and raised the riparian water table by up to 1·0 m. Increased hydraulic gradients inland from the stream limited the entry of oxic nitrate‐rich subsurface water from adjacent cropland. Permeable riparian sediments overlying dense till remained saturated during the summer and autumn months, whereas before dam construction a large area of the riparian zone was unsaturated in these seasons each year. Beaver dam construction produced significant changes in riparian groundwater chemistry. Median dissolved oxygen concentrations were lower in riparian groundwater after dam construction (0·9–2·1 mg L^?1) than in the pre‐dam period (2·3–3·9 mg L^?1). Median NO₃‐N concentrations in autumn and spring were also lower in the post‐dam (0·03–0·07 mg L^?1) versus the pre‐dam period (0·1–0·3 mg L^?1). In contrast, median NH₄‐N concentrations in autumn and spring months were higher after dam construction (0·3–0·4 mg L^?1) than before construction (0·13–0·14 mg L^?1). Results suggest that beaver dams can increase stream inflow to riparian areas that limit water table declines and increase depths of saturated riparian soils which become more anaerobic. These changes in subsurface hydrology and chemistry have the potential to affect the transport and transformation of nitrate fluxes from adjacent cropland in agricultural landscapes. Copyright © 2009 John Wiley & Sons, Ltd.     

大型水库分层期和混合期溶存温室气体空间变化及排放通量

水库作为温室气体的重要来源,对区域气候变化有不可忽略的影响。然而,目前对水库溶存温室气体的空间异质性及垂向特征的认知仍然欠缺。为了揭示水库分层期和混合期溶存温室气体空间特征及排放通量,也为厘清水库温室气体产生和排放的关键过程提供重要支撑。研究选择东北地区大型水库——汤河水库为对象,于2021年7—9月和10月(分别代表水库分层期和混合期)对水库不同位置(坝前、库中和库尾)开展溶存温室气体垂向分层监测。研究结果显示,水库CH₄排放通量变化范围为0.018～0.174 mmol/(m²·d),是大气CH₄的源,空间分布为库尾>库中>坝前;CO₂通量为-4.91～58.77 mmol/(m²·d),除分层期东支库尾,其余点位均表现为大气CO₂的源,空间分布为坝前>库中>库尾。时间上,分层期CH₄排放通量(0.071±0.044 mmol/(m²·d))高于混合期((0.027±0.008) mm...     

Influence of Atmospheric Solar Radiation Absorption on Photodestruction of Ions at D-Region Altitudes of the Ionosphere

The influence of atmospheric solar radiation absorption on the photodetachment, dissociative photodetachment, and photodissociation rate coefficients (photodestruction rate coefficients) of O^?, Cl^?, O₂ ^?, O₃ ^?, OH^?, NO₂ ^?, NO₃ ^?, O₄ ^?, OH^?(H₂O), CO₃ ^?, CO₄ ^?, ONOO^?, HCO₃ ^?, CO₃ ^?(H₂O), NO₃ ^?(H₂O), O₂ ⁺(H₂O), O₄ ⁺, N₄ ⁺, NO⁺(H₂O), NO⁺(H₂O)₂, H⁺(H₂O) _n for n = 2–4, NO⁺(N₂), and NO⁺(CO₂) at D-region altitudes of the ionosphere is studied. A numerical one-dimensional time-dependent neutral atmospheric composition model has been developed to estimate this influence. The model simulations are carried out for the geomagnetically quiet time period of 15 October 1998 at moderate solar activity over the Boulder ozonesonde. If the solar zenith angle is not more than 90° then the strongest influence of atmospheric solar radiation absorption on photodestruction of ions is found for photodissociation of CO₄ ^? ions when CO₃ ^? ions are formed. It follows from the calculations that decreases in the photodestruction rate coefficients of ions under consideration caused by this influence are less than 2 % at 70 km altitude and above this altitude if the solar zenith angle does not exceed 90°.     

Experimental study on N<Subscript>2</Subscript>O and CH<Subscript>4</Subscript> fluxes from the dark coniferous forest zone soil of the Gongga Mountain,China

The static closed chamber technique is used in the study on the CH₄ and N₂O fluxes from the soils of primeval Abies fabri forest, the succession Abies fabri forest and the clear-cut areas of mid-aged Abies fabri forest in the Gongga Mountain from May 1998 to September 1999. The results indicate the following: (i) The forest soil serves as the source of atmospheric N₂O at the three measurement sites, while the fluxes of CH₄ are all negative, and soil is the sink of atmospheric CH₄. The comparative relations of N₂O emissions between the three sites are expressed as primeval Abies fabri forest < clear-cut areas < succession Abies fabri forest, and those of CH₄ consumption fluxes are primeval Abies fabri forest < succession Abies fabri forest < clear-cut areas, (ii) Significant seasonal variations of N₂O emission at various sites were observed, and two emission peaks of N₂O occurr during summer (July—August) and spring (February—March), whereas N₂O emission is relatively low in winter and spring (mid March—April). Seasonal variations of CH₄ consumption at each measurement site fluctuate drastically with unclear regularities. Generally, CH₄ consumption fluxes of succession Abies fabri forest and clear-cut areas are higher from mid May to late July but lower in the rest of sampling time, while the CH₄ flux keeps a relatively high value even up to September in primeval Abies fabri forest. In contrast to primeval Abies fabri forest, the CH₄ absorbabilities of succession Abies fabri forest and clear-cut areas of mid-aged Abies fabri forest are weaker. Particularly, the absorbability of the clear-cut areas is even weaker as compared with the other two sites, for the deforestation reduces the soil absorbability of atmospheric CH₄. (iii) Evident diurnal variation regularity exists in the N₂O emissions of primeval Abies fabri forest, and there is a statistic positive correlation between the fluxes of N₂O and air temperature (R=0.95, n=11, α· 0.01), and also the soil temperature of 5-cm layer (R=0.81, n=11, α> 0.01), whereas the CH₄ diurnal variation regularities are unclear and have no significant correlation with the soil temperature of 5-cm layer and air temperature.     

Greenhouse gas emissions (CO2, CH4, and N2O) from several perialpine and alpine hydropower reservoirs by diffusion and loss in turbines

We investigated greenhouse gas emissions (CO₂, CH₄, and N₂O) from reservoirs located across an altitude gradient in Switzerland. These are the first results of greenhouse gas emissions from reservoirs at high elevations in the Alps. Depth profiles were taken in 11 reservoirs located at different altitudes between the years 2003 and 2006. Diffusive trace gas emissions were calculated using surface gas concentrations, wind speeds and transfer velocities. Additionally, methane entering with the inflowing water and methane loss at the turbine was assessed for a subset of the reservoirs. All reservoirs were emitters of carbon dioxide and methane with an average of 970?±?340?mg?m^?2?day^?1 (results only from four lowland and one subalpine reservoir) and 0.20?±?0.15?mg?m^?2?day^?1, respectively. One reservoir (Lake Wohlen) emitted methane at a much higher rate (1.8?±?0.9?mg?m^?2?day^?1) than the other investigated reservoirs. There was no significant difference in methane emissions across the altitude gradient, but average dissolved methane concentrations decreased with increasing elevation. Only lowland reservoirs were sources for N₂O (72?±?22???g?m^?2?day^?1), while the subalpine and alpine reservoirs were in equilibrium with atmospheric concentrations. These results indicate reservoirs from subalpine/alpine regions to be only minor contributors of greenhouse gases to the atmosphere compared to other reservoirs.     

三峡水库澎溪河水-气界面CO2、CH4扩散通量昼夜动态初探

三峡水库温室气体效应近年来备受关注.为揭示三峡水库典型支流澎溪河水-气界面CO₂和CH₄通量的昼夜动态规律,明晰短时间尺度下该水域温室气体释放的影响因素,在2010年6月至2011年5月的一个完整水文周年内,选择4个具有代表性的时段(2010年8、11月和2011年2、5月)对澎溪河高阳平湖水域开展昼夜跟踪观测.结果表明:2010年8、11月和2011年2、5月4次采样的CO₂日总通量值分别为-8.34、73.94、28.13和-20.12 mmol/(m²·d),相应的CH₄日总通量值分别为2.22、0.11、0.32和7.16 mmol/(m²·d),不同时期昼夜变化明显.研究水域CO₂和CH₄通量过程不具同步性:CO₂昼夜通量变化可能更显著地受到水柱光合/呼吸过程的影响,但瞬时气象过程(水汽温差、瞬时风速等)在高水位时期亦可对CO₂通量产生显著影响;CH₄昼夜通量变化与水温条件改变更为密切.     

Hydrological flowpaths and nitrate removal rates within a riparian floodplain along a fourth‐order stream in Brittany (France)

Three main reservoirs were identified that contribute to the shallow subsurface flow regime of a valley drained by a fourth‐order stream in Brittany (western France). (i) An upland flow that supplied a wetland area, mainly during the high‐water period. It has high N‐NO₃^? and average Cl^? concentrations. (ii) A deep confined aquifer characterized by low nitrate and low chloride concentrations that supplied the floodplain via flow upwelling. (iii) An unconfined aquifer under the riparian zone with high Cl^? and low N‐NO₃^? concentrations where biological processes removed groundwater nitrate. This aquifer collected the upland flow and supplied a relict channel that controlled drainage from the whole riparian zone. Patterns of N‐NO₃^? and Cl^? concentrations along riparian transects, together with calculated high nitrate removal, indicate that removal occurred mainly at the hillslope–riparian zone interface (i.e. first few metres of wetland), whereas dilution occurred in lower parts of the transects, especially during low‐water periods and at the beginning of recharge periods. Stream flow was modelled as a mixture of water from the three reservoirs. An estimation of these contributions revealed that the deep aquifer contribution to stream flow averaged 37% throughout the study period, while the contribution of the unconfined reservoir below the riparian zone and hillslope flow was more variable (from ca 6 to 85%) relative to rainfall events and the level of the riparian water table. At the entire riparian zone scale, NO₃^? removal (probably from denitrification) appeared most effective in winter, despite higher estimated upland NO₃^? fluxes entering the riparian zone during this period. Copyright © 2003 John Wiley & Sons, Ltd.     

The oxygen minimum zone (OMZ) off Chile as intense source of CO2 and N2O

The oxygen minimum zones (OMZs) are recognized as intense sources of N₂O greenhouse gas (GHG) and could also be potential sources of CO₂, the most important GHG for the present climate change. This study evaluates, for one of the most intense and shallow OMZ, the Chilean East South Pacific OMZ, the simultaneous N₂O and CO₂ fluxes at the air–sea interface. Four cruises (2000–2002) and 1 year of monitoring (21°–30°–36°S) off Chile allowed the determination of the CO₂ and N₂O concentrations at the sea surface and the analysis of fluxes variations associated with different OMZ configurations. The Chilean OMZ area can be an intense GHG oceanic local source of both N₂O and CO₂. The mean N₂O fluxes are 5–10 times higher than the maximal previous historical source in an OMZ open area as in the Pacific and Indian Oceans. For CO₂, the mean fluxes are also positive and correspond to very high oceanic sources. Even if different coupling and decoupling between N₂O and CO₂ are observed along the Chilean OMZ, 65% of the situations represent high CO₂ and/or N₂O sources. The high GHG sources are associated with coastal upwelling transport of OMZ waters rich in N₂O and probably also in CO₂, located at a shallow depth. The integrated OMZ role on GHG should be better considered to improve our understanding of the past and future atmospheric CO₂ and N₂O evolutions.     

Soil CO2 flux baseline in an urban monogenetic volcanic field: the Auckland Volcanic Field, New Zealand

The Auckland Volcanic Field (AVF) is a dormant monogenetic basaltic field located in Auckland, New Zealand. Though soil gas CO₂ fluxes are routinely used to monitor volcanic regions, there have been no published studies of soil CO₂ flux or soil gas CO₂ concentrations in the AVF to date or many other monogenetic fields worldwide. We measured soil gas CO₂ fluxes and soil gas CO₂ concentrations in 2010 and 2012 in varying settings, seasons, and times of day to establish a baseline soil CO₂ flux and to determine the major sources of and controlling influences on Auckland's soil CO₂ flux. Soil CO₂ flux measurements varied from 0 to 203 g m^?2 day^?1, with an average of 27.1 g m^?2 day^?1. Higher fluxes were attributed to varying land use properties (e.g., landfill). Using a graphical statistical approach, two populations of CO₂ fluxes were identified. Isotope analyses of δ¹³CO₂ confirmed that the source of CO₂ in the AVF is biogenic with no volcanic component. These data may be used to assist with eruption forecasting in the event of precursory activity in the AVF, and highlight the importance of knowing land use history when assessing soil gas CO₂ fluxes in urban environments.     

Etude de la phase gazeuse occluse dans les laves de «l’Ardoukôba», volcan éphémère d’une dorsale émergée (Afar)

Gases trapped in lavas of three main flows of the Ardoukôba eruption (8 to 15 November, 1978) have been analysed by mass spectrometry. These analyses concern both plagioclase phenocrysts and microcrystalline mesostasis. Fluids are released between 500°C and 1200°C, and consist of H₂O, CO₂, CO, N₂, SO₂, HCl, H₂, CH₄ with traces of hydrocarbons and H₂S. The total content is less than 0.3–0.4 wt. % of samples with about 0.1–0.15 wt % of H₂O. No significant variation among the three flows is observed. Plagioclase phenocrysts are less abundant in fluids than the mesostasis (～2/3). The gases trapped in these phenocrysts are richer in CO and organic compounds, whereas mesostasis contain more H₂O, CO₂ and SO₂. CO is likely produced by reduction of CO₂ and H₂O with carbon during either analyses or eruption itself, or is of primary origin. In the latter case, gas composition suggests an entrapment temperature of about 1200°C ± 75°C. Kinetic study of the water and carbon dioxide release allows to calculate the diffusion characteristics of these fluids. Water and carbon dioxide behave rather similarly. Plagioclase gives a single activation energy value (8 Kcal/mole), while mesostasis gives two values (8 Kcal/mole, 15 Kcal/mole). Diffusion coefficients at 20°C are estimated to fall in the range 10^?13 · 10^?12 cm² · sec^?1.     

Supersaturation and evasion of CO2 and CH4 in surface waters at Mer Bleue peatland,Canada

Carbon dioxide (CO₂) and methane (CH₄) concentrations and evasion rates were measured in surface waters draining Mer Bleue peatland (Ontario, Canada) between spring and autumn 2005. All sites exhibit a consistent pattern of supersaturation throughout the year, which is broadly related to hydrological and temperature changes between spring snowmelt and autumn freezing. Both measurements and estimates of CO₂ and CH₄ evasion from open water to the atmosphere suggest that parts of the catchment (including beaver dams) are significant degassing hot spots. We present data showing how vertical gaseous carbon fluxes compare with lateral carbon fluxes and make an initial estimate of the importance to the overall carbon budget of CO₂ and CH₄ evasion to the atmosphere from water surfaces at Mer Bleue. Copyright © 2007 John Wiley & Sons, Ltd.     

Nitrous Oxide Emissions in Sewer Systems

Nitrous oxide emissions from urban wastewater were measured in a combined sewer in Bayreuth, Germany. The closed-chamber method was used to evaluate N₂O emissions. Nitrous oxide was analysed by gas chromatography with electron capture detector. Longitudinal and daily variations of N₂O fluxes were determined. N₂O emissions ranged from 0.11…3.8 mg m^?2 h^?1 depending on the level of wastewater in the sewer. Data indicate that N₂O is mainly formed in the biofilm by nitrification and/or denitrification. In laboratory experiments, samples with wastewater and wastewater/biofilm mixture were incubated with and without NaCl. After two hours of incubation, N₂O release was in a range of 42…429 ng N₂O per millilitre wastewater or wastewater/biofilm. Incubated samples without NaCl addition showed no significant difference between wastewater and wastewater/biofilm mixture. If salt (NaCl) was added before incubation, samples with wastewater/biofilm mixture emitted 4.8 times more N₂O than wastewater samples. It is assumed that high concentrations of NaCl inhibit further microbial reduction of N₂O to N₂. Based on the field data, a first estimate for N₂O emission from sewers is 3.5 g N₂O per year and person.     

Long‐term carbon storage and hydrological control of CO2 exchange in tundra ponds in the Hudson Bay Lowland

Carbon dioxide fluxes and water balance were examined in 43 tundra ponds in the northern portion of the Hudson Bay Lowland near Churchill, Manitoba. Most of the ponds were hydrologically disconnected from their catchments during dry periods throughout the post‐melt season. However, episodic reconnection occurred following large precipitation events where depression storage was exceeded. Significant shifts in pond chemistry were observed following precipitation events, with the degree of CO₂ saturation increasing during these periods. Pond CO₂ concentrations rapidly fell to pre‐event levels following events, suggesting that hydrological connectivity can affect the magnitude and direction of CO₂ gas fluxes in tundra ponds. Atmospheric CO₂ invaded ponds with highly organic sediments for most of the summer, suggesting that terrestrially derived inorganic carbon was insufficient to meet the demands of algal net production. In contrast, ponds with highly mineral sediments continued to evade CO₂ during the summer. In a subset of 11 ponds, long‐term rates of carbon accumulation in sediment ranged from 0·6 to 2·2 mol C m^?2 year^?1. Very strong correlations existed between average sediment accumulation rates and pond perimeters and basin areas suggesting that peat may be a major source of sediment carbon. Aeolian transport is also a potentially large source of sediment carbon. Copyright © 2004 John Wiley & Sons, Ltd.