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  • Articles  (44)
  • methane  (44)
  • Springer  (44)
  • National Academy of Sciences
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  • 1
    Electronic Resource
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    Springer
    Climatic change 40 (1998), S. 277-284 
    ISSN: 1573-1480
    Keywords: ombrotrophic bogs ; microbial ecology ; methane ; climate change
    Source: Springer Online Journal Archives 1860-2000
    Topics: Geosciences , Physics
    Notes: Abstract Gases are produced from wetlands when plant biomass is degraded by microbial consortia, producing carbon dioxide aerobically and methane when oxygen is lacking. In anaerobic waterlogged situations, such as the catotelm of ombrotrophic bogs, this methane forms minute gas bubbles that severely reduce the hydraulic conductivity and hence the degradation of biomass due to the lack of nutrients. The bogs thus become carbon sinks, formed from the partially degraded biomass that accumulates as peat. The results of an investigation of an ombrotrophic bog, Mer Bleue, Ontario, Canada are summarized here, and the effects that climate change may have on such bogs are discussed. Any change of the water table in wetlands will have a substantial effect upon their ecology. If the water table should fall allowing bogs to become aerobic, most of the accumulated biomass carbon could be returned to the atmosphere by degradation to carbon dioxide, and as well, methane entrapped within the matrix would be released directly to the atmosphere. If on the other hand, the bogs are flooded, then the entrapped bubbles will coalesce allowing the gas to escape to the atmosphere, while at the same time the degradation of the peat will be enhanced.
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  • 2
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    Geotechnical and geological engineering 4 (1986), S. 217-233 
    ISSN: 1573-1529
    Keywords: Coal ; methane ; adsorption ; desorption
    Source: Springer Online Journal Archives 1860-2000
    Topics: Geosciences
    Notes: Summary During an investigation to study the gas flow characteristics of coal, adsorption and desorption rates of methane from powdered coal samples were measured. From adsorption tests, it was found that the capacity of coal to hold methane varies significantly with gas pressure. For pressures up to 4.14 MPa (600 psi) the amount of gas adsorbed was still rising and monomolecular saturation was not reached. Results of desorption tests were used to test three equations suggested by previous investigators to measure the quantity of desorbed gas. It was confirmed that no single equation would define adequately the complete desorption process. Changes of regime appeared to exist at desorption times of 100 s and, to a lesser extent, 1000 s following the initial release of ambient gas pressure. A hypothesis was advanced that initial flow was inhibited or choked by an efflux of desorbing gas molecules. This was followed by a short transitional period and a longer term regime of free flow with reduced resistance offered by the flow paths.
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  • 3
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    Aquatic geochemistry 4 (1998), S. 403-427 
    ISSN: 1573-1421
    Keywords: methane ; trace gases ; North Sea ; air-sea exchange
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology , Geosciences
    Notes: Abstract The methane concentration in the atmosphere andsurface water was surveyed along 58° N acrossthe North Sea. In addition, the vertical methanedistribution in the water column was determined at sixstations along the transect. The methane contents ofthe surface water as well as in the water column wereextremely inhomogeneous. Input by freshwater fromriver discharge and injection of methane from thesediment were both observed. The survey continued fromthe western side of the North Sea to the Elbe Riverestuary. The Elbe River appears to have low methaneconcentrations compared to other European rivers, itsaverage input into the North Sea is estimated to be70 nmol s-1 of methane. Near 58° N,1°40' E, an abandoned drill site releases about 25 % ofthe North Sea's emission of methane to the atmosphere.The advective methane transport induced by watercirculation was assessed for May 16, 1994, using a 3-DNorth Sea circulation model. For the period of thissurvey, the North Sea's source strength foratmospheric methane is estimated using in situwind velocities. In comparison to the advectivetransport by the water circulation, the gas flux tothe atmosphere appears to be the dominant sink ofNorth Sea methane. This flux is estimated to bebetween 1500 · 106 mol a-1 and 3100 ·106mol a-1, depending on the relationbetween wind speed and gas transfer velocity.
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  • 4
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    Biogeochemistry 47 (1999), S. 15-23 
    ISSN: 1573-515X
    Keywords: ethane ; groundwater ; methane ; propane ; redox ; soil gas
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology , Geosciences
    Notes: Abstract This study investigates the presence and concentration of light hydrocarbon gases in soil vapor located immediately above the capillary fringe of a petroleum-contaminated aquifer. A correlation was observed for the linear regression plot of redox potential versus detectable C2+C3 alkane concentrations for a limited number of sampling points. C2+C3 alkanes were not detected at points were redox potentials in groundwater exceeded --260 millivolts. The predominance of methanogenic processes in this redox range, as well as the observed C2+C3 concentration ratios, suggest that ethane and propane gases in soil vapor may be biogenically produced as well as a result of volatilization from NAPL.
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  • 5
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    Biogeochemistry 47 (1999), S. 15-23 
    ISSN: 1573-515X
    Keywords: ethane ; groundwater ; methane ; propane ; redox ; soil gas
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology , Geosciences
    Notes: Abstract This study investigates the presence and concentration of light hydrocarbon gases in soil vapor located immediately above the capillary fringe of a petroleum-contaminated aquifer. A correlation was observed for the linear regression plot of redox potential versus detectable C2+C3 alkane concentrations for a limited number of sampling points. C2+C3 alkanes were not detected at points were redox potentials in groundwater exceeded -260 millivolts. The predominance of methanogenic processes in this redox range, as well as the observed C2+C3 concentration ratios, suggest that ethane and propane gases in soil vapor may be biogenically produced as well as a result of volatilization from NAPL.
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  • 6
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    Biogeochemistry 6 (1988), S. 201-210 
    ISSN: 1573-515X
    Keywords: dimethylsulfide ; methane thiol ; sulfate ; methane ; sulfate reduction ; methanogenesis ; anaerobic methane oxidation
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology , Geosciences
    Notes: Abstract Seasonal variation of dimethylsulfide (DMS) and methane thiol (MSH) concentrations in sediment porewater was determined in a Danish estuary. Dimethylsulfide (DMDS) was never found. Detectable DMS levels of up to 0.1 μM were found only in the summer and only within the upper 5 cm of the sediment. The DMS accumulation was probably associated with decomposing fragments of macro-algae in the surface layer. Significant MSH accumulation of up to 1 μM was found only in the deep, CH4-rich sediment below the SO4 2- zone. With depth, a detectable MSH level could thus be observed below the 1 mM SO4 2--isopleth which also marked the SO4 2--CH4 transition. The transition zone was located deeper in the sediment in winter (20–25 cm depth) than in summer (5–10 cm depth). The absence of MSH in the SO4 2- zone could be due to rapid utilization of the compound by SO4 2--reducing bacteria. A possible involvement of MSH in anaerobic CH4 oxidation at the transition zone is discussed; CH4 and sulfide (HS- form, pH 7) are proposed to form MSH and H2 which in turn may be metabolized by, e.g. SO4 2--reducing bacteria.
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  • 7
    ISSN: 1573-515X
    Keywords: carbon dioxide ; hysteresis ; methane ; peat ; temperature ; wetlands
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology , Geosciences
    Notes: Abstract The ability to predict the effects of climate change on trace gas fluxes requires a knowledge of microbial temperature responses. However, the response of a microbial community to temperature in a given substrate may be complicated by its thermal history. To examine the effect of sequentially changing temperature on methane and carbon dioxide production in different peat types, we incubated anaerobic peat samples from 3 types of northern peatlands, a bog, a sedge fen and a cedar swamp, in both rising and falling temperature regimes. Graphic and statistical comparisons of the different temperature regimes suggest hysteresis in microbial response to temperature, although the absolute rates at any given temperature often did not differ. Where regressions for temperature response (Arrhenius plots) were significant, they generally differed between temperature regimes. The greatest differences among treatments occurred during the first half of the 40-d incubation. Increases in carbon dioxide production were similar across all peat types, but methanogenesis varied widely: methane production was uniformly low in the bog peat but increased sharply with temperature in the other two peat types. The complicating effect of history or chronology on substrate responses to environmental stimuli may restrain our ability to model the responses of complex systems to changing conditions.
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  • 8
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    Biogeochemistry 37 (1997), S. 227-236 
    ISSN: 1573-515X
    Keywords: Louisiana USA ; wetlands ; methane ; methanogensis
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology , Geosciences
    Notes: Abstract Methane emissions from three wetland habitats in the MississippiRiver deltaic plain were measured over a three year period. Fluxdata collected indicate that each habitat was a net source of methane to the atmosphere throughout the year. Average emissionfrom a Taxodium distichum / Nyssa aquatica (bald cypress / watertupelo) swamp forest was 146 ± 199 mgCH4 m-2d-1 whileemissions from a Sagittaria lancifolia (bulltongue) freshwatermarsh averaged 251 ± 188 mg CH4m-2d-1. Methane flux from a Spartina patens / Sagittaria lancifolia intermediate marsh was significantlyhigher, 912 ± 923 mg CH4m-2d-1. Seasonal variation wassignificant with emissions being higher in the late summer andearly fall. Significant diurnal emissions were observed fromthe Sagittaria lancifolia marsh site. Soil temperature (5 and 10 cm depths) was found to be significantly correlated with methaneemission from the three sites.
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  • 9
    ISSN: 1573-515X
    Keywords: drainage ; denitrification ; methane ; nitric oxide ; nitrous oxide ; nitrification
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology , Geosciences
    Notes: Abstract Intermittent drainage of rice fields isdiscussed as an option to mitigate emission ofCH4, an important greenhouse gas. HoweverN2O, a potentially more effective greenhouse gas,may be emitted during the aeration phase. Therefore,the metabolism of NO, N2O, NH $$_4^ + $$ ,NO $$_2^ - $$ and NO $$_3^ - $$ and the kinetics ofCH4 oxidation were measured after aeration ofmethanogenic rice field soil. Before aeration, thesoil contained NH $$_4^ + $$ in relatively highconcentrations (about 4 mM), while NO $$_2^ - $$ andNO $$_3^ - $$ were almost undetectable. Immediatelyafter aeration both NO and N2O were produced withrates of about 15 pmol h-1 gdw-1 and 5 pmolh-1 gdw-1, respectively. Simultaneously,NH $$_4^ + $$ decreased while NO $$_2^ - $$ accumulated. Later on, NO $$_2^ - $$ was depletedwhile NO $$_3^ - $$ concentrations increased.Characteristic phases of nitrogen turnover wereassociated with the activities of ammonium oxidizers,nitrite oxidizers and denitrifiers. Oxidation ofNH $$_4^ + $$ and production of NO and N2O wereinhibited by 10 Pa acetylene demonstrating thatnitrification was obligatory for the initiation ofnitrogen turnover and production of NO and N2O.Ammonium oxidation was not limited by the availableNH $$_4^ + $$ and thus, concomittant production of NOand N2O was not stimulated by addition ofNH $$_4^ + $$ . However, addition of NO $$_3^ - $$ stimulated production of NO and N2O in bothanoxic and aerated rice soil slurries. In this case,10 Pa acetylene did not inhibit the production of NOand N2O demonstrating that it was due todenitrification which was obviously limited by theavailability of NO $$_3^ - $$ . In the aerated soilslurries CH4 was only oxidized if present atelevated concentrations 〉50 ppmv CH4). Atatmospheric CH4 concentrations (∼1.7 ppmv)CH4 was not consumed, but was even slightly produced.CH4 oxidation activity increased afterpreincubation at 20% CH4, and then CH4was also oxidized at atmospheric concentrations. CH4oxidation kinetics exhibited sigmoid characteristicsat low CH4 concentrations presumably because ofinhibition of CH4 oxidation by NH $$_4^ + $$ .
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  • 10
    ISSN: 1573-515X
    Keywords: Atlantic ; ethylene ; methane ; sea-air exchange
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology , Geosciences
    Notes: Abstract The vertical distributions of ethylene and methane in the upper water column of the subtropical Atlantic were measured along a transect from Madeira to the Caribbean and compared with temperature, salinity, oxygen, nutrients, chlorophyll-a, and dissolved organic carbon (DOC). Methane concentrations between 41.6 and 60.7 nL L−1 were found in the upper 20 m of the water column giving a calculated average flux of methane into the atmosphere of 0.82μg m−2 h−1. Methane profiles reveal several distinct maxima in the upper 500 m of the water column and short-time variations which are presumably partly related to the vertical migration of Zooplankton. Ethylene concentrations in near surface waters varied in the range of 1.8 to 8.2 nL L−1. Calculated flux rates for ethylene into the atmosphere were in the range of 0.41 to 1.35μg m−2 h−1 with a mean of 0.83μg m−2h−2. Maximum concentrations of up to 39.2 nL L−2 were detected directly below the pycnocline in the western Atlantic. The vertical distributions of ethylene generally showed one maximum at the pycnocline (about 100 m depth) where elevated concentrations of chlorophyll-a, dissolved oxygen, and nutrients were also found; no ethylene was detected below 270 m depth. This suggests that ethylene release is mainly related to one, probably phytoplankton associated, source, while for methane, enhanced net production occurs at various depth horizons. For surface waters, a simple correlation between ethylene and chlorophyll-a or DOC concentrations could not be observed. No considerable diurnal variation was observed for the distribution and concentration of ethylene in the upper water column.
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  • 11
    ISSN: 1573-515X
    Keywords: grassland ; methane ; peat ; spatial variability ; wetland
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology , Geosciences
    Notes: Abstract Methane (CH4) emissions from soils, representing the consequence of CH4 production, CH4 consumption and CH4 transport, are poorly characterised and show a large spatial variability. This study aimed to assess the determinants of field-scale spatial variability of CH4 emissions from wet grasslands on peat soil. Mean CH4 emission rates of a three-year experiment at 18 plots distributed over three sites in the nature preserve “Nieuwkoopse Plassen” on peat soil in the Netherlands were related to CH4 production and CH4 consumption capacities of soil layers, and to soil and vegetation characteristics. Spatial variability of CH4 emissions and possible determining factors was high. Annual CH4 emissions ranged from 3 to 37 g CH4 m-2 yr-1. Coefficients of variation (CV) of CH4 emissions were on average 37% among sites and 83% within sites. Most important determinants of spatial variability were CH4 production capacity (average: 211 ng CH4 g-1 dry soil h-1; CV: 131%) and aboveground biomass of sedges (Carex spp.) (average: 0.45 g dm-2; CV: 127%) (P 〈 0.01). Sedges may affect CH4 emissions by stimulating CH4 transport from anaerobic layers to the surface via their vascular system and/or by serving as substrate for methanogens. For extrapolation of CH4 emissions to larger areas, best results will be obtained by using factors that are easy to determine, like vegetation.
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  • 12
    ISSN: 1573-515X
    Keywords: grassland ; ground water level ; methane ; peat ; temperature ; wetland
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology , Geosciences
    Notes: Abstract The area of wet grasslands on peat soil in the Netherlands is slowly increasing at the expense of drained, agriculturally used grasslands. This study aimed (i) to assess the contribution of wet grasslands on peat soil to methane (CH4) emissions, and (ii) to explain differences among sites and between years in order to improve our understanding of controlling factors. For these purposes, a field study was conducted in the period 1994–1996 in the nature preserve “Nieuwkoopse Plassen”, which is a former peat mining and agricultural area. Net CH4 emissions were measured weekly to monthly with vented closed flux chambers at three representative sites, and at ditches near these sites. Three-years average of CH4 emissions was 7.9 g CH4 m- 2 yr-1 for Drie Berken Zudde, 13.3 for Koole, and 20.4 for Brampjesgat. Ditches near the sites emitted 4.2–22.5 g CH4 m-2 yr-1. The time-course of CH4 emissions for all experimental sites and years was fit with a multiple linear regression model with ground water level and soil temperature as independent variables. Lowering or raising the ground water level by 5 cm could decrease or increase CH4 emissions by 30–50%. Therefore, ground water level management of these grasslands should be done with care.
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  • 13
    ISSN: 1573-515X
    Keywords: climate ; methane ; N2O ; Puerto Rico ; soil oxygen ; soil phosphorus
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology , Geosciences
    Notes: Abstract We measured soil oxygen concentrations at 10 and 35 cm depths and indices of biogeochemical cycling in upland forest soils along a rainfall and elevation gradient (3500–5000 mm y−1; 350–1050 masl) and along topographic gradients (ridge to valley, ∼150 m) in the Luquillo Experimental Forest, Puerto Rico. Along the rainfall gradient, soil O2 availability decreased significantly with increasing annual rainfall, and reached very low levels (〈3%) in individual chambers for up to 25 consecutive weeks over 82 weeks of study. Along localized topographic gradients, soil O2 concentrations were variable and decreased significantly from ridges to valleys. In the valleys, up to 35% of the observations at 10–35 cm depth were 〈3% soil O2. Cross correlation analyses showed that soil O2 concentrations were significantly positively correlated along the topographic gradient, and were sensitive to rainfall and hydrologic output. Soil O2 concentrations in valley soils were correlated with rainfall from the previous day, while ridge sites were correlated with cumulative rainfall inputs over 4 weeks. Soils at the wettest point along the rainfall gradient had very high soil methane concentrations (3–24%) indicating a strong influence of anaerobic processes. We measured net methane emission to the atmosphere at the wettest sites of the rainfall gradient, and in the valleys along topographic gradients. Other measures of biogeochemical function such as soil organic matter content and P availability were sensitive to chronic O2 depletion along the rainfall gradient, but less sensitive to the variable soil O2 environment exhibited at lower elevations along topographic gradients.
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  • 14
    ISSN: 1573-515X
    Keywords: alpine tundra ; methane ; trace gas
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology , Geosciences
    Notes: Abstract We measured CH4 fluxes from three major plant communities characteristic of alpine tundra in the Colorado Front Range. Plant communities in this ecosystem are determined by soil moisture regimes induced by winter snowpack distribution. Spatial patterns of CH4 flux during the snow-free season corresponded roughly with these plant communities. InCarex-dominated meadows, which receive the most moisture from snowmelt, net CH4 production occurred. However, CH4 production in oneCarex site (seasonal mean=+8.45 mg CH4 m−2 d−1) was significantly larger than in the otherCarex sites (seasonal means=−0.06 and +0.05 mg CH4 m−2 d−1). This high CH4 flux may have resulted from shallower snowpack during the winter. InAcomastylis meadows, which have an intermediate moisture regime, CH4 oxidation dominated (seasonal mean=−0.43 mg CH4 m−2 d−1). In the windsweptKobresia meadow plant community, which receive the least amount of moisture from snowmelt, only CH4 oxidation was observed (seasonal mean=−0.77 mg CH4 m−2 d−1). Methane fluxes correlated with a different set of environmental factors within each plant community. In theCarex plant community, CH4 emission was limited by soil temperature. In theAcomastylis meadows, CH4 oxidation rates correlated positively with soil temperature and negatively with soil moisture. In theKobresia community, CH4 oxidation was stimulated by precipitation. Thus, both snow-free season CH4 fluxes and the controls on those CH4 fluxes were related to the plant communities determined by winter snowpack.
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  • 15
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    Biogeochemistry 47 (1999), S. 187-202 
    ISSN: 1573-515X
    Keywords: boreal peatland ; floating peat ; methane ; reservoirs ; wetlands
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology , Geosciences
    Notes: Abstract The effect of flooding on methane (CH4) fluxes was studied through the construction of an experimental reservoir in a boreal forest wetland at the Experimental Lakes Area in northwestern Ontario. Prior to flooding, the peatland surface was a small source of CH4 to the atmosphere (1.0 ± SD of 2.3 mg CH4 m−2 d−1). After flooding, CH4 fluxes from the submerged peat surface increased to 64±68 mg CH4 m−2 d−1. CH4 bubbles within the submerged peat caused about 1/3 of the peat to float. Fluxes from these floating peat islands were much higher (440±350 mg CH4 m−2 d−1) than from both the pre-flood (undisturbed) and the post-flood (submerged) peat surfaces. The high fluxes of CH4 from the floating peat surfaces may be explained by a number of factors known to affect the production and consumption of CH4 in peat. In floating peat, however, these factors are particularly enhanced and include decreased oxidation of CH4 due to the loss of aerobic habitat normally found above the water table of undisturbed peat and to increased peat temperatures. The extremely high fluxes associated with newly lifted peat may decrease as the islands age. However, CH4 flux rates from floating peat islands that were several years old still far exceeded those from undisturbed peat surfaces and from the water surface of a newly created reservoir.
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  • 16
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    Biogeochemistry 47 (1999), S. 187-202 
    ISSN: 1573-515X
    Keywords: boreal peatland ; floating peat ; methane ; reservoirs ; wetlands
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology , Geosciences
    Notes: Abstract The effect of flooding on methane (CH4) fluxes was studied through the construction of an experimental reservoir in a boreal forest wetland at the Experimental Lakes Area in northwestern Ontario. Prior to flooding, the peatland surface was a small source of CH4 to the atmosphere (1.0± SD of 2.3 mg CH4 m−2 d−1). After flooding, CH4 fluxes from the submerged peat surface increased to 64±68 mg CH4 m−2 d−1 CH4 bubbles within the submerged peat caused about 1/3 of the peat to float. Fluxes from these floating peat islands were much higher (440±350 mg CH4 m−2 d−2) than from both the pre-flood (undisturbed) and the post-flood (submerged) peat surfaces. The high fluxes of CH4 from the floating peat surfaces may be explained by a number of factors known to affect the production and consumption of CH4 in peat. In floating peat, however, these factors are particularly enhanced and include decreased oxidation of CH4 due to the loss of aerobic habitat normally found above the water table of undisturbed peat and to increased peat temperatures. The extremely high fluxes associated with newly lifted peat may decrease as the islands age. However, CH4 flux rates from floating peat islands that were several years old still far exceeded those from undisturbed peat surfaces and from the water surface of a newly created reservoir.
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  • 17
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    Climatic change 40 (1998), S. 229-245 
    ISSN: 1573-1480
    Keywords: carbon ; carbon dioxide ; methane ; dissolved organic carbon ; peatlands ; climatic change
    Source: Springer Online Journal Archives 1860-2000
    Topics: Geosciences , Physics
    Notes: Abstract Northern peatlands play an important role globally in the cycling of C, through the exchange of CO2 with the atmosphere, the emission of CH4, the production and export of dissolved organic carbon (DOC) and the storage of C. Under 2 × CO2 GCM scenarios, most Canadian peatlands will be exposed to increases in mean annual temperature ranging between 2 and 6° C and increases in mean annual precipitation of 0 to 15 %, with the most pronounced changes occurring during the winter. The increase in CO2 uptake by plants, through warmer temperatures and elevated atmospheric CO2, is likely to be offset by increased soil respiration rates in response to warmer soils and lowered water tables. CH4 emissions are likely to decrease in most peatlands because of lowered water tables, except where the peat surface adjusts to fluctuating water tables, and in permafrost, where the collapse of dry plateau and palsa will lead to increase CH4 emission. There likely will be little change in DOC production, but DOC export to water bodies will decrease as runoff decreases. The storage of C in peatlands is sensitive to all C cycle components and is difficult to predict. The challenge is to develop quantitative models capable of making these predictions for different peatlands. We present some qualitative responses, with levels of uncertainty. There will be, however, as much variation in response to climatic change within a peatland as there will be among peatland regions.
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  • 18
    ISSN: 1573-0662
    Keywords: biomass burning ; hydrocarbons ; methane
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology , Geosciences
    Notes: Abstract Atmospheric samples from savanna burnings were collected in the Ivory Coast during two campaigns in January 1989 and January 1991. About 30 nonmethane hydrocarbons from C2 to C6, carbon monoxide, carbon dioxide and methane were measured from the background and also at various distances from the burning. Concentrations in the fire plume reached ppmv levels for C2-C4 hydrocarbons, and 5300, 500 and 93 ppmv for CO2, CO and CH4 respectively. The excess in the mixing ratios of these gases above their background level is used to derive emission factors relative to CO and CO2. For the samples collected immediately in the fire plume, a differentiation between high and low combustion efficiency conditions is made by considering the CO/CO2 ratio. Ethene (C2H4), acetylene (C2H2), ethane (C2H6) and propene (C3H6) are the major NMHC produced in the flaming stage, whereas a different pattern with an increasing contribution of alkanes is observed in samples typical of post flaming processes. A strong correlation between methane and carbon monoxide suggests that these compounds are produced during the same stage of the combustion. In samples collected at a distance from the fire and integrated over a period of 30 minutes, the composition is very similar to that of flaming. ΔNMHC/ΔCO2 is of the order of 0.7%, ΔCH4/ΔCO2 of the order of 0.4% and ΔCO/ΔCO2 of the order of 6.3%. From this study, a global production by African savanna fires is derived: 65 Tg of CO-C, 4.2 Tg of CH4-C and 6.7 Tg of NMHC-C. Whereas acetylene can be used as a conservative tracer of the fire plumes, only ethene, propene and butenes can be considered in terms of their direct photochemical impact.
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  • 19
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    Journal of atmospheric chemistry 23 (1996), S. 37-49 
    ISSN: 1573-0662
    Keywords: Ab initio ; methane ; chlorine ; kinetic isotope effect
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology , Geosciences
    Notes: Abstract Recent studies suggest that the destruction of methane by Cl• in the marine boundary layer could be accounted for as another major sink besides the methane destruction by OH•. High level ab initio molecular orbital calculations have been carried out to study the CH4+Cl• reaction, the carbon Kinetic Isotope Effect (KIE) is calculated using Conventional Transition-State Theory (CTST) plus Wigner and Eckart semiclassical tunneling corrections. The calculated KIE is around 1.026 at 300 K and has a small temperature variation. This is by far the largest KIE among different processes involving atmospheric methane destruction (e.g., OH•, soil). A calculated mass balance of atmospheric methane including the KIE for the CH4+Cl• reaction is found to favor those methane budgets with enhanced biological methane sources, which have relatively lighter carbon isotope composition.
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  • 20
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    Journal of atmospheric chemistry 9 (1989), S. 81-99 
    ISSN: 1573-0662
    Keywords: Arctic ; atmosphere ; methane ; carbon dioxide ; haze ; correlation ; AGASP
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology , Geosciences
    Notes: Abstract Fifty flask air samples were taken during April 1986 from a NOAA WP-3D Orion aircraft which flew missions across a broad region of the Arctic as part of the second Arctic Gas and Aerosol Sampling Program (AGASP II). The samples were subsequently analyzed for both carbon dioxide (CO2) and methane (CH4). The samples were taken in well-defined layers of Arctic haze, in the background troposphere where no haze was detected, and from near the surface to the lower stratosphere. Vertical profiles were specifically measured in the vicinity of Barrow, Alaska to enable comparisons with routine surface measurements made at the NOAA/GMCC observatory. Elevated levels of both methane and carbon dioxide were found in haze layers. For samples taken in the background troposphere we found negative vertical gradients (lower concentrations aloft) for both gases. For the entire data set (including samples collected in the haze layers) we found a strong positive correlation between the methane and carbon dioxide concentrations, with a linear regression slope of 17.5 ppb CH4/ppm CO2, a standard error of 0.6, and a correlation coefficient (r2) of 0.95. This correlation between the two gases seen in the aircraft samples was corroborated by in situ surface measurements of these gases made at the Barrow observatory during March and April 1986. We also find a similar relationship between methane and carbon dioxide measured concurrenty for a short period in the moderately polluted urban atmosphere of Boulder, Colorado. We suggest that the strong correlation between methane and carbon dioxide concentrations reflects a common source region for both, with subsequent long-range transport of the polluted air to the Arctic.
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  • 21
    ISSN: 1573-0662
    Keywords: Atmospheric background concentrations ; ozone ; carbondioxide ; carbon isotopes ; methane ; optical thickness ; North Atlantic ; long-range transport
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology , Geosciences
    Notes: Abstract First results of baseline observations from the new BAPMoN station Tenerife give information about the atmospheric background in this latitude of about 25° N in the North Atlantic. The influence of the meridional exchange with the northern part of the hemisphere as well as transport from the African continent is evident. Changes of air mass are strongly reflected in the concentration records of carbon dioxide, methane, and ozone depending on the seasonal and meridional distribution of these components. Transport of Sahara dust results in an increase of optical thickness and an ozone depletion. According to the seasonal frequency of characteristic transport conditions, these influences are reflected in the annual cycle of the records.
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  • 22
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    Journal of atmospheric chemistry 8 (1989), S. 153-164 
    ISSN: 1573-0662
    Keywords: Carbon monoxide ; methane ; global distribution ; seasonal variations ; trends ; spectroscopic measurements
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology , Geosciences
    Notes: Abstract A spectroscopic technique for measuring CO and CH4 contents is described and the latitudinal distributions of these gases are presented. Carbon monoxide abundance decreases southward, having two local maxima: in midlatitudes and in the tropics. The slope of latitude dependence varies according to the season of the year. The difference in CH4 content does not exceed the accuracy of the method (±8%).
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  • 23
    ISSN: 1573-0662
    Keywords: Trace gases ; methane ; carbon monoxide ; nitrous oxide ; distribution ; tropospheric-stratospheric exchange
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology , Geosciences
    Notes: Abstract During aircraft flights in May 1981 from Munich (40°N) to north of the Spitsbergen Islands (82°N) and to Monrovia, Liberia (6°N), air samples were obtained in the altitude range of 8 to 11 km and during the ascents and descents near the airports. These samples have been analyzed for the trace gas mixing ratios of CH4, CO and N2O. The results of these analyses are presented and discussed. The results provide new evidence of tropospheric-stratospheric exchange events in the vicinity of the subpolar and subtropical tropopause foldings and possibly show a case of transport of CO-enriched air in the upper troposphere above the North Atlantic Ocean.
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  • 24
    ISSN: 1573-0662
    Keywords: Carbon monoxide ; methane ; latitudinal distribution ; spectroscopic measurements ; Arctic ; Antarctic
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology , Geosciences
    Notes: Abstract The results of spectroscopic total column measurements of CO and CH4 at different points of the Northern and Southern Hemispheres in 1970–1985, are reported. Seasonal cycles of CO are evident for all the sites. The Northern Hemispheric long-term positive trend of CO seems to be 1.5–2% per year. In the Southern Hemisphere, temporal increasing was not detected and a possible upper limit for it is about 0.6% per year. Methane concentration in the Northern Hemisphere increases at a rate of 1.2% per year.
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  • 25
    ISSN: 1573-0662
    Keywords: tropospheric chemistry ; ozone ; Russia ; trans-Siberian railroad ; Siberia ; carbon monoxide ; methane ; nitrogen oxides ; trace gases ; atmospheric composition
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology , Geosciences
    Notes: Abstract Using a laboratory wagon traveling along the Trans-Siberian railroad, O3, NO, NO2, CO, CH4, SF6 and black carbon aerosol have been measured during the summer of 1996. The expedition from Niznij Novgorod (500 km east of Moscow) to Vladivostok (and back to Moscow) has shown the great potential of the train method; here the first results are presented and discussed. A wealth of boundary layer air data was obtained during the over 18000 km travel without serious contamination problems from the electric train itself. The diurnal O3 cycle peaked generally below 50 nmole/mole, showed the effects of changes in J(NO2), and often dropped to a few nmole/mole at night time during inversions. Over the vast Siberian lowlands situated between the Ural mountains and the river Yenisey, CH4 levels were consistently elevated at around 1.95 µmole/mole, which we mainly attribute to wetland emissions. Over eastern Siberia, however, CH4 levels were generally lower at 1.85 µmole/mole. In contrast, over the west Siberian lowlands, CO levels were relatively low, often reaching values of only 110 nmole/mole, whereas over eastern Siberia CO levels were higher. Very high CO levels were detected over a 2000 km section east of Chita, along the river Amur, which represented an enormous polluted air mass. 14C analysis performed on several CO samples confirms that the origin was biomass burning. SF6, which was measured as a general conserved tracer, showed an eastward attenuation from 4.0 to 3.9 pmole/mole, with peaks in a number of places due to local Russian emissions.
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  • 26
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    Biogeochemistry 31 (1995), S. 155-173 
    ISSN: 1573-515X
    Keywords: methane ; methanogenesis ; arid-lands ; Sonoran Desert ; streams ; hydrologic exchange
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology , Geosciences
    Notes: Abstract Methanogenesis was studied in five streams of central and southern Arizona by examining the distribution of methane in interstitial water and evasion of methane in three subsystems (hyporheic, parafluvial and bank sediments). In Sycamore Creek, the primary study site (studied during summer and early autumn), methane content of interstitial water exhibited a distinct spatial pattern. In hyporheic (sediments beneath the wetted channel) and parfluvial zones (active channel sediments lateral to the wetted channel), which were well oxygenated due to high hydrologic exchange with the surface stream and had little particulate organic matter (POM), interstitial methane concentration averaged only 0.03 mgCH4-C/L. Bank sediments (interface between the active channel and riparian zone), in contrast, which were typically vegetated, had high POM, low hydrologic exchange and concomitantly low dissolved oxygen levels, had interstitial concentration averaging 1.5 mgCH4-C/L. Methane emission from Sycamore Creek, similar to methane concentration, averaged only 3.7 mgCH4-C·m−2·d−1 from hyporheic and parafluvial zones as opposed to 170 mgCH4-C·m−2·d−1 from anoxic bank sediments. Methane in four additional streams sampled (one sampling date during late winter) was low and exhibited little spatial variation most likely due to cooler stream temperatures. Interstitial methane in parafluvial and bank sediments of all four streams ranged from only 0.005 to 0.1 mgCH4-C/L. Similarly methane evasion was also low from these streams varying from 0 to 5.7 mgCH4-C·m−2·d−1. The effects of organic matter and temperature on methanogenesis were further examined by experimentally manipulating POM and temperature in stoppered flasks filled with hyporheic sediments and stream water. Methane production significantly increased with all independent variables. Methane production is greatest in bank sediments that are relatively isolated hydrologically and lowest in hyporheic and parafluvial sediments that are interactive with the surface stream.
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  • 27
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    Biogeochemistry 34 (1996), S. 57-70 
    ISSN: 1573-515X
    Keywords: Cladium jamaicense ; Eleocharis spp. ; Typha domingensis ; interstitial water ; methane ; sulfate ; northern Belize
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology , Geosciences
    Notes: Abstract Wetlands of northern Belize provide a unique opportunity to study methane production and emissions from marshes dominated by identical species (Typha domingensis, Cladium jamaicense) and genus (Eleocharis spp.), but differing substantially in the amount of sulfates present in the sediments. Some marshes occur on limestone marls rich in gypsum (CaSO4) while others are underlain by alluvial sands poor in sulfates. Concentrations of methane and sulfates in the sediment interstitial water are one or more orders of magnitude different for these two geological substrata averaging 139.2 and 14.9 μM of CH4, and 0.08 and 11.53 mM of SO4 −2 2 on alluvial sands and limestone respectively. The amount of methane found in the internal atmosphere of plants from alluvial sands is significantly higher (6.3 μM) than in plants from limestone (0.19 μM). The average methane emissions measured in wetlands located on alluvial sands were 25.2 mg m−2 h−1 while emissions from marshes on limestone were only 2.4 mg m−2 h−1. These values extrapolated for the entire year and the respective wetland areas resulted in the estimate of total CH4 emissions from northern Belize of 0.066 Tg per year.
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  • 28
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    Biogeochemistry 37 (1997), S. 77-88 
    ISSN: 1573-515X
    Keywords: climate change ; elevated carbon dioxide ; hydrology ; methane ; transpiration ; wetlands
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology , Geosciences
    Notes: Abstract Methane emissions from wetland soils are generally a positive function ofplant size and primary productivity, and may be expected to increase dueto enhanced rates of plant growth in a future atmosphere of elevatedCO2. We performed two experiments with Orontium aquaticum, acommon emergent aquatic macrophyte in temperate and sub-tropical wetlands, todetermine if enhanced rates of photosynthesis in elevated CO2atmospheres would increase CH4 emissions from wetland soils.O. aquaticum was grown from seed in soil cores under ambient and elevated(ca. 2-times ambient) concentrations of CO2 in an initialglasshouse study lasting 3 months and then a growth chamber study lasting 6months. Photosynthetic rates were 54 to 71% higher underelevated CO2 than ambient CO2, but plantbiomass was not significantly different at the end of the experiment. Ineach case, CH4 emissions were higher under elevated thanambient CO2 levels after 2 to 4 months of treatment, suggestinga close coupling between photosynthesis and methanogenesis in our plant-soilsystem. Methane emissions in the growth chamber study increased by 136%. We observed a significant decrease in transpirationrates under elevated CO2 in the growth chamber study, andspeculate that elevated CO2 may also stimulate CH4 emissions by increasing the extent and duration offlooding in some wetland ecosystems. Elevated CO2 maydramatically increase CH4 emissions from wetlands, a sourcethat currently accounts for 40% of global emissions.
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  • 29
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    Biogeochemistry 41 (1998), S. 215-235 
    ISSN: 1573-515X
    Keywords: arctic ; carbon dioxide ; climate change ; methane ; plant transport ; species composition
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology , Geosciences
    Notes: Abstract We conducted plant species removals, air temperaturemanipulations, and vegetation and soil transplants inAlaskan wet-meadow and tussock tundra communities todetermine the relative importance of vegetation typeand environmental variables in controlling ecosystemmethane (CH4) and carbon dioxide (CO2) flux. Plastic greenhouses placed over wet-meadow tundraincreased air temperature, soil temperature, and soilmoisture, but did not affect CH4 or CO2 flux(measured in the dark). By contrast, removal ofsedges in the wet meadow significantly decreased fluxof CH4, while moss removal tended to increaseCH4 emissions. At 15 cm depth, pore-waterCH4 concentrations were higher in sedge-removalthan in control plots, suggesting that sedgescontribute to CH4 emissions by transportingCH4 from anaerobic soil to the atmosphere, ratherthan by promoting methanogenesis. Inreciprocal-ecosystem transplants between thewet-meadow and tussock tundra communities, CH4and CO2 emissions were higher overall in thewet-meadow site, but were unrelated to transplantorigin. Methane flux was correlated with localvariation in soil temperature, thaw depth, andwater-table depth, but the relative importance ofthese factors varied through the season. Our resultssuggest that future changes in CH4 and CO2flux in response to climatic change will be morestrongly mediated by large-scale changes in vegetationand soil parameters than by direct temperature effects.
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  • 30
    ISSN: 1573-515X
    Keywords: alpine tundra ; methane ; trace gas
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology , Geosciences
    Notes: Abstract We measured CH4 fluxes from three major plant communities characteristic of alpine tundra in the Colorado Front Range. Plant communities in this ecosystem are determined by soil moisture regimes induced by winter snowpack distribution. Spatial patterns of CH4 flux during the snow-free season corresponded roughly with these plant communities. In Carex-dominated meadows, which receive the most moisture from snowmelt, net CH4 production occurred. However, CH4 production in one Carex site (seasonal mean = +8.45 mg CH4 m-2 d-1) was significantly larger than in the other Carex sites (seasonal means = –0.06 and +0.05 mg CH4 m-2 d-1). This high CH4 flux may have resulted from shallower snowpack during the winter. In Acomastylis meadows, which have an intermediate moisture regime, CH4 oxidation dominated (seasonal mean = –0.43 mg CH4 m-2 d-1). In the windswept Kobresia meadow plant community, which receive the least amount of moisture from snowmelt, only CH4 oxidation was observed (seasonal mean = –0.77 mg CH4 m-2 d-1). Methane fluxes correlated with a different set of environmental factors within each plant community. In the Carex plant community, CH4 emission was limited by soil temperature. In the Acomastylis meadows, CH4 oxidation rates correlated positively with soil temperature and negatively with soil moisture. In the Kobresia community, CH4 oxidation was stimulated by precipitation. Thus, both snow-free season CH4 fluxes and the controls on those CH4 fluxes were related to the plant communities determined by winter snowpack.
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  • 31
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    Biogeochemistry 28 (1995), S. 183-200 
    ISSN: 1573-515X
    Keywords: methane ; methanogenesis ; transport ; tundra
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology , Geosciences
    Notes: Abstract The roles of plant transport and CH4 production in controlling CH4 flux from wet meadow tundra communities were investigated. Plant transport was the dominant pathway of CH4 flux from this ecosystem. Most CH4 production (measured within situ anaerobic incubations) occurred well below the water table, and C supply (estimated by anaerobic CO2 production) was the best single predictor of CH4 production rates. Plant transport of CH4 was controlled both by CH4 supply and the plant species.Eriophorum angustifolium transported substantially more CH4 than didCarex aquatilis, due to differences in size and structure of the two species. The composition of the plant community was a greater control on CH4 flux from the site than either water table height (which varied only slightly) or CH4 production rates, indicating the importance of species-specific plant dynamics in controlling CH4 flux from arctic wetlands.
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  • 32
    ISSN: 1573-515X
    Keywords: aquatic marcrophytes ; methane ; methane oxidation ; methyl fluoride ; plant/microbial ; interactions ; rhizosphere
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology , Geosciences
    Notes: Abstract Methane oxidation rates in the rhizosphere of Pontederia cordata,Sagittaria lancifolia, and Typha latifolia were quantified in fieldstudies using the methyl fluoride inhibition technique. An averageoxidation of 22.9 ± 17.7% (sd,n = 44) was found for all field experiments (oxidation is expressedas a % of total potential emission in the presumedabsence of oxidation). Greenhouse experiments using the same techniquegave an average rhizospheric oxidation of 64.9 ±17.0% (sd, n = 44). Comparison of a subset ofgreenhouse plants with the methyl fluoride (MF) and a light oxic/darkanoxic (LO/DA) technique for suppressing CH4 oxidationyielded similar percentages (57.7 ±15.0% for MF and 58.5 ±13.9% for LO/DA, n = 11). Rhizospheric oxidationdisplayed a seasonal trend in Typha latifolia with decreasingoxidation percentages during warmer months as the importance ofrhizospheric CH4 oxidation declined relative toCH4 emission (46.5 ±13.8% in December and 13.5 ±1.7% in July). However, the absolute rateof methane oxidation was highest during the warmer months (44.2± 3.4 mg m-2 d-1 inDecember and 318.7 ± 151.4 mg m-2d-1 in July). As methane emission rates increased,the sensitivity of the methyl fluoride technique decreased dueto the larger error between replicate flux measurements.
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  • 33
    ISSN: 1573-515X
    Keywords: die-back ; methane ; methanogenesis ; Phragmites australis ; rhizosphere
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology , Geosciences
    Notes: Abstract Methanogenesis was measured during the summer of 1994, in sediment coresand bulk samples from a Phragmites australis wetland in northern Jutland,Denmark. We compared sediment from healthy reed and dying-back reed, andan open lagoon resulting from die-back. Cores revealed variability withdepth and between sites, with the highest rates coinciding with layers oforganic gyttja, and negligible methane production from the underlying sandbase. Methanogenesis rates in the lagoon and die back sites were higher(up to 100–150 nmol h-1 g-1dry wt. sediment) than in the healthy reed (50–80 nmolh-1 g-1), with the highest rates being recordedfrom May to July. At these times, methanogenesis was markedly temperature-limited; samples incubated at 30 °C anon-limiting temperature, gave rates as high as 200–400nmol h-1 g-1 for the lagoon and die-backareas and 150 nmol h-1 g-1 for the healthyarea. Addition of 8 mM acetate and H2/CO2headspace suggested that both acetate-fermenting andCO2-reducing bacteria were present. Acetate additions suggested some co-limitation by substrate availability, with acetate limitation occurring in the healthy site during July and in the die-back site during August. Lower rates during August, especially in the healthy area, were associated with low water levels which resulted in more oxidized sediments. The data reveal highly variable methanogenesis in the sediment which, when considered with sediment depths, indicates that sites of Phragmites die-back have significantly greater rates of anaerobic mineralization than surrounding healthy wetland, and may be intense sources of methane.
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  • 34
    ISSN: 1573-515X
    Keywords: autochthonous organic matter ; carbon dioxide ; decomposition ; methane ; nitrous oxide ; δ13C
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology , Geosciences
    Notes: Abstract The vertical distribution of dissolved greenhouse gases (CH4,ΣCO2 and N2O), NO $${\text{NO}}_{\text{2}} - $$ ,and δ13C of ΣCO2 in Lake Biwa during a stagnantperiod was precisely determined. ΣCO2 as well as NO $${\text{NO}}_{\text{3}} - $$ was accumulated in the hypolimnion, whereas NO $${\text{NO}}_{\text{2}} - $$ and CH4concen\-trations were generally higher in theepilimnion than in the hypolimnion. In August, NO $${\text{NO}}_{\text{2}} - $$ andCH4 were ephemerally accumulated at the thermocline. Theconcentration of CH4 always exceeded equilibrium with respectto air/water exchange. N2O was rather uniformly distributed inboth time and space, and remained near equilibrium with respect toair/water exchange. All of these observations are similar to otherstratified, oligotrophic lakes, in which the hypolimnia were welloxygenated. The δ13C of ΣCO2 became morenegative with increasing depth, and showed a strong negativecorrelation with apparent oxygen utilization. From the data, the δ13Cvalue of organic matter decomposed into ΣCO2 inthe hypolimnion was calculated by isotope mass-balance, and found tobe in a similar range to δ13C of phytoplankton and benthic algaeand distinctively higher than δ13C of both terrestrial andsedimentary organic matters. This suggests that autochthonous organicmatter was the major source of ΣCO2.
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  • 35
    ISSN: 1573-515X
    Keywords: glucosidase ; methane ; peat ; phosphatase ; sulphate ; sulphatase ; wetland
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology , Geosciences
    Notes: Abstract Possible interactions between soil enzymes and thebiogeochemistry of wetlands were investigated duringa field-based drought simulation. Under control(waterlogged) conditions, correlations were foundbetween the activity of the enzyme B-glucosidase andtwo properties associated with carbon cycling, namelyi) CH4 release r = 0.79,p lt 0.01) and ii) dissolvedorganic carbon concentration (r= -0.81, p lt 0.01). In contrast,the transition to drought conditions resulted in correlations betweenB-glucosidase activity and certain mineralisationprocesses, namely the release of mg and Ca(r = 0.72, p lt 0.05). Sulphataseactivity correlated with changes in sulphate concentration during the droughtsimulation (r = 0.73, p lt 0.05).Further support for the suggested enzymic involvement in biogeochemicalprocesses was found in laboratory studies. Theseexperiments indicated that increasing the abundance ofB-glucosidase could stimulate trace gas emissions(p lt 0.001) and increase the concentration ofmagnesium and calcium (p lt 0.05). Increasedsulphatase abundance caused a suppression of methane emissions(p = 0.053).
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  • 36
    ISSN: 1573-515X
    Keywords: carbon dioxide ; carbon mineralization ; fermentation ; methane ; sulfate reduction ; West Virginia ; wetland
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology , Geosciences
    Notes: Abstract The mineralization of organic carbon to CH4 and CO2 inSphagnum-derived peat from Big Run Bog, West Virginia, was measured at 4 times in the year (February, May, September, and November) using anaerobic, peat-slurry incubations. Rates of both CH4 production and CO2 production changed seasonally in surface peat (0–25 cm depth), but were the same on each collection date in deep peat (30–45 cm depth). Methane production in surface peat ranged from 0.2 to 18.8 μmol mol(C)−1 hr−1 (or 0.07 to 10.4 μg(CH4) g−1 hr−1) between the February and September collections, respectively, and was approximately 1 μmol mol(C)−1 hr−1 in deep peat. Carbon dioxide production in surface peat ranged from 3.2 to 20 μmol mol(C)−1 hr−1 (or 4.8 to 30.3 μg(CO2) g−1 hr−1) between the February and September collections, respectively, and was about 4 μmol mol(C)−1 hr−1 in deep peat. In surface peat, temperature the master variable controlling the seasonal pattern in CO2 production, but the rate of CH4 production still had the lowest values in the February collection even when the peat was incubated at 19°C. The addition of glucose, acetate, and H2 to the peat-slurry did not stimulate CH4 production in surface peat, indicating that CH4 production in the winter was limited by factors other than glucose degradation products. The low rate of carbon mineralization in deep peat was due, in part, to poor chemical quality of the peat, because adding glucose and hydrogen directly stimulated CH4 production, and CO2 production to a lesser extent. Acetate was utilized in the peat by methanogens, but became a toxin at low pH values. The addition of SO4 2− to the peat-slurry inhibited CH4 production in surface peat, as expected, but surprisingly increased carbon mineralization through CH4 production in deep peat. Carbon mineralization under anaerobic conditions is of sufficient magnitude to have a major influence on peat accumulation and helps to explain the thin (〈 2 m deep), old (〉 13,000 yr) peat deposit found in Big Run Bog.
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  • 37
    ISSN: 1573-515X
    Keywords: carbon dioxide ; eastern Tennessee ; ecosystem metabolism ; methane ; streams ; Smoky Mountains
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology , Geosciences
    Notes: Abstract The partial pressures of CO2 (pCO2) andCH4 (pCH4) in streams are not only governed byinstream processes, but also by transformations occurring in soil andgroundwater ecosystems. As such, stream water pCO2 andpCH4 can provide a tool to assess ecosystem respiration andanaerobic metabolism throughout drainage basins. We conducted three surveyssampling the gas content of streams in eastern Tennessee and western NorthCarolina to assess factors regulating ecosystem metabolism in catchmentswith contrasting geomorphologies, elevations and soil organic matterstorage. In our first survey, the influence of drainage basin geomorphologyon ecosystem respiration was examined by sampling streams drainingcatchments underlain by either shale or dolomite. Geomorphology isinfluenced by geology with shale catchments having shallower soils, broader,unconstrained valley floors compared with dolomite catchments.pCO2 varied little between catchment types but increased froman average of 3340 ppmv in spring to 9927 ppmv in summer or 9.3 and 28 timesatmospheric equilibrium (pCO2(equilib)), respectively. Incontrast, pCH4 was over twice as high in streams drainingshale catchments (306 ppmv; pCH4(equilib) = 116) compared withmore steeply incised dolomite basins (130 ppmv; pCH4(equilib)= 51). Using the ratio of pCH4:pCO2 as an indexof anaerobic metabolism, shale catchments had nearly twice as muchanaerobiosis (pCH4:pCO2 = 0.046) than dolomitedrainages (pCH4:pCO2 = 0.024). In our secondsurvey, streams were sampled along an elevational gradient (525 to 1700 m)in the Great Smoky Mountains National Park, USA where soil organic matterstorage increases with elevation. pCO2 did not vary betweenstreams but increased from 5340 ppmv (pCO2(equilib) = 15) to8565 ppmv (pCO2(equilib) = 24) from spring to summer,respectively. During spring pCH4 was low and constant acrossstreams, but during summer increased with elevation ranging from 17 to 2068ppmv (pCH4(equilib) = 10 to 1216). The contribution ofanaerobiosis to total respiration was constant during spring(pCH4:pCO2 = 0.017) but during summer increasedwith elevation from 0.002 at 524 m to 0.289 at 1286 m. In our last survey,we examined how pCO2 and pCH4 changed withcatchment size along two rivers (ca. 60 km stretches in both riverscorresponding to increases in basin size from 1.7–477km2 and 2.5–275 km2). pCO2and pCH4 showed opposite trends, with pCO2decreasing ca. 50% along the rivers, whereas pCH4roughly doubled in concentration downstream. These opposing shifts resultedin a nearly five-fold increase of pCH4:pCO2along the rivers from a low of 0.012 in headwaters to a high of 0.266 65-kmdownstream. pCO2 likely declines moving downstream asgroundwater influences on stream chemistry decreases, whereaspCH4 may increase as the prevalence of anoxia in riversexpands due to finer-grained sediments and reduced hydrologic exchange withoxygenated surface water.
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  • 38
    ISSN: 1573-515X
    Keywords: Atlantic ; ethylene ; methane ; sea-air exchange
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology , Geosciences
    Notes: Abstract The vertical distributions of ethylene and methane in the upper water column of the subtropical Atlantic were measured along a transect from Madeira to the Caribbean and compared with temperature, salinity, oxygen, nutrients, chlorophyll-a, and dissolved organic carbon (DOC). Methane concentrations between 41.6 and 60.7 nL L-1 were found in the upper 20 m of the water column giving a calculated average flux of methane into the atmosphere of 0.82 μg m-2 h-1. Methane profiles reveal several distinct maxima in the upper 500 m of the water column and short-time variations which are presumably partly related to the vertical migration of zooplankton. Ethylene concentrations in near surface waters varied in the range of 1.8 to 8.2 nL L-1. Calculated flux rates for ethylene into the atmosphere were in the range of 0.41 to 1.35 μg m-2 h-1 with a mean of 0.83 μg m-2 h-1. Maximum concentrations of up to 39.2 nL L-1 were detected directly below the pycnocline in the western Atlantic. The vertical distributions of ethylene generally showed one maximum at the pycnocline (about 100 m depth) where elevated concentrations of chlorophyll-a, dissolved oxygen, and nutrients were also found; no ethylene was detected below 270 m depth. This suggests that ethylene release is mainly related to one, probably phytoplankton associated, source, while for methane, enhanced net production occurs at various depth horizons. For surface waters, a simple correlation between ethylene and chlorophyll-a or DOC concentrations could not be observed. No considerable diurnal variation was observed for the distribution and concentration of ethylene in the upper water column.
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  • 39
    ISSN: 1573-515X
    Keywords: carbon dioxide ; gas gradients ; methane ; nitrous oxide ; peatland ; winter
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology , Geosciences
    Notes: Abstract CO2 and CH4 fluxes during the winter were measured at natural and drained bog and fen sites in eastern Finland using both the closed chamber method and calculations of gas diffusion along a concentration gradient through the snowpack. The snow diffusion results were compared with those obtained by chamber, but the winter flux estimates were derived from chamber data only. CH4 emissions from a poor bog were lower than those from an oligotrophic fen, while both CO2 and CH4 fluxes were higher in the Carex rostrata-occupied marginal (lagg) area of the fen than in the slightly less fertile centre. Average estimated winter CO2-C losses from virgin and drained forested peatlands were 41 and 68 g CO2-C m- 2, respectively, accounting for 23 and 21% of the annual total CO2 release from the peat. The mean release of CH4-C was 1.0 g in natural bogs and 3.4 g m-2 in fens, giving rise to winter emissions averaging to 22% of the annual emission from the bogs and 10% of that from the fens. These wintertime carbon gas losses in Finnish natural peatlands were even greater than reported average long-term annual C accumulation values (less than 25 g C m-2). The narrow range of 10–30% of the proportion of winter CO2 and CH4 emissions from annual emissions found in Finnish peatlands suggest that a wider generalization in the boreal zone is possible. Drained forested bogs emitted 0.3 g CH4-C m-2 on the average, while the effectively drained fens consumed an average of 0.01 g CH4-C m- 2. Reason for the low CH4 efflux or net oxidation in drained peatlands probably lies in low substrate supply and thus low CH4 production in the anoxic deep peat layers. N2O release from a fertilized grassland site in November–May was 0.7 g N2O m-2, accounting for 38% of the total annual emission, while a forested bog released none and two efficiently drained forested fens 0.09 (28% of annual release) and 0.04 g N2O m- 2 (27%) during the winter, respectively.
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  • 40
    ISSN: 1573-515X
    Keywords: carbon dioxide ; gas gradients ; methane ; nitrous oxide ; peatland ; winter
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology , Geosciences
    Notes: Abstract CO2 and CH4 fluxes during the winter were measured at natural and drained bog and fen sites in eastern Finland using both the closed chamber method and calculations of gas diffusion along a concentration gradient through the snowpack. The snow diffusion results were compared with those obtained by chamber, but the winter flux estimates were derived from chamber data only. CH4 emissions from a poor bog were lower than those from an oligotrophic fen, while both CO2 and CH4 fluxes were higher in theCarex rostrata- occupied marginal (lagg) area of the fen than in the slightly less fertile centre. Average estimated winter CO2-C losses from virgin and drained forested peatlands were 41 and 68 g CO2-C m−2, respectively, accounting for 23 and 21% of the annual total CO2 release from the peat. The mean release of CH4-C was 1.0 g in natural bogs and 3.4 g m−2 in fens, giving rise to winter emissions averaging to 22% of the annual emission from the bogs and 10% of that from the fens. These wintertime carbon gas losses in Finnish natural peatlands were even greater than reported average long-term annual C accumulation values (less than 25g C m−2). The narrow range of 10–30% of the proportion of winter CO2 and CH4 emissions from annual emissions found in Finnish peatlands suggest that a wider generalization in the boreal zone is possible. Drained forested bogs emitted 0.3 g CH4-C m−2 on the average, while the effectively drained fens consumed an average of 0.01 g CH4-C m−2. Reason for the low CH4. efflux or net oxidation in drained peatlands probably lies in low substrate supply and thus low CH4 production in the anoxic deep peat layers. N2O release from a fertilized grassland site in November–May was 0.7 g N2O m−2, accounting for 38% of the total annual emission, while a forested bog released none and two efficiently drained forested fens 0.09 (28% of annual release) and 0.04 g N2O m−2 (27%) during the winter, respectively.
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  • 41
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    Biogeochemistry 44 (1999), S. 205-220 
    ISSN: 1573-515X
    Keywords: grassland ; ground water level ; methane ; peat ; temperature ; wetland
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology , Geosciences
    Notes: Abstract The area of wet grasslands on peat soil in the Netherlands is slowly increasing at the expense of drained, agriculturally used grasslands. This study aimed (i) to assess the contribution of wet grasslands on peat soil to methane (CH4) emissions, and (ii) to explain differences among sites and between years in order to improve our understanding of controlling factors. For these purposes, a field study was conducted in the period 1994–1996 in the nature preserve “Nieuwkoopse Plassen”, which is a former peat mining and agricultural area. Net CH4 emissions were measured weekly to monthly with vented closed flux chambers at three representative sites, and at ditches near these sites. Three-years average of CH4 emissions was 7.9 g CH4 m−2 yr−1 for Drie Berken Zudde, 13.3 for Koole, and 20.4 for Brampjesgat. Ditches near the sites emitted 4.2–22.5 g CH4 m−2 yr−1. The time-course of CH4 emissions for all experimental sites and years was fit with a multiple linear regression model with ground water level and soil temperature as independent variables. Lowering or raising the ground water level by 5 cm could decrease or increase CH4 emissions by 30–50%. Therefore, ground water level management of these grasslands should be done with care.
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  • 42
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    Biogeochemistry 44 (1999), S. 221-237 
    ISSN: 1573-515X
    Keywords: grassland ; methane ; peat ; spatial variability ; wetland
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology , Geosciences
    Notes: Abstract Methane (CH4) emissions from soils, representing the consequence of CH4 production, CH4 consumption and CH4 transport, are poorly characterised and show a large spatial variability. This study aimed to assess the determinants of field-scale spatial variability of CH4 emissions from wet grasslands on peat soil. Mean CH4 emission rates of a three-year experiment at 18 plots distributed over three sites in the nature preserve “Nieuwkoopse Plassen” on peat soil in the Netherlands were related to CH4 production and CH4 consumption capacities of soil layers, and to soil and vegetation characteristics. Spatial variability of CH4 emissions and possible determining factors was high. Annual CH4 emissions ranged from 3 to 37 g CH4 m−2 yr−1. Coefficients of variation (CV) of CH4 emissions were on average 37% among sites and 83% within sites. Most important determinants of spatial variability were CH4 production capacity (average: 211 ng CH4 g−1 dry soil h−1; CV: 131%) and aboveground biomass of sedges (Carex spp.) (average: 0.45 g dm−2; CV: 127%) (P〈0.01). Sedges may affect CH4 emissions by stimulating CH4 transport from anaerobic layers to the surface via their vascular system and/or by serving as substrate for methanogens. For extrapolation of CH4 emissions to larger areas, best results will be obtained by using factors that are easy to determine, like vegetation.
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  • 43
    ISSN: 1573-515X
    Keywords: climate ; methane ; N2O ; Puerto Rico ; soil oxygen ; soil phosphorus
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology , Geosciences
    Notes: Abstract We measured soil oxygen concentrations at 10 and 35 cm depths and indices of biogeochemical cycling in upland forest soils along a rainfall and elevation gradient (3500–5000 mm y−1; 350–1050 masl) and along topographic gradients (ridge to valley, ∼150 m) in the Luquillo Experimental Forest, Puerto Rico. Along the rainfall gradient, soil O2 availability decreased significantly with increasing annual rainfall, and reached very low levels (〈3%) in individual chambers for up to 25 consecutive weeks over 82 weeks of study. Along localized topographic gradients, soil O2 concentrations were variable and decreased significantly from ridges to valleys. In the valleys, up to 35% of the observations at 10–35 cm depth were 〈3% soil O2. Cross correlation analyses showed that soil O2 concentrations were significantly positively correlated along the topographic gradient, and were sensitive to rainfall and hydrologic output. Soil O2 concentrations in valley soils were correlated with rainfall from the previous day, while ridge sites were correlated with cumulative rainfall inputs over 4 weeks. Soils at the wettest point along the rainfall gradient had very high soil methane concentrations (3–24%) indicating a strong influence of anaerobic processes. We measured net methane emission to the atmosphere at the wettest sites of the rainfall gradient, and in the valleys along topographic gradients. Other measures of biogeochemical function such as soil organic matter content and P availability were sensitive to chronic O2 depletion along the rainfall gradient, but less sensitive to the variable soil O2 environment exhibited at lower elevations along topographic gradients.
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  • 44
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    Geotechnical and geological engineering 5 (1987), S. 353-368 
    ISSN: 1573-1529
    Keywords: Ventilation ; recirculation ; transients ; methane
    Source: Springer Online Journal Archives 1860-2000
    Topics: Geosciences
    Notes: Summary This paper discusses the development of a mathematical model to describe the unsteady airflow created and the subsequent effect on both the production and transportation of methane around the recirculation zone. Examples of the response of a single face recirculation system to various disturbances are presented and discussed.
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