Flooding of the continental shelves as a contributor to deglacial CH4 rise

The transition from the last glacial and beginning of Bølling–Allerød and Pre‐Boreal periods in particular is marked by rapid increases in atmospheric methane (CH₄) concentrations. The CH₄ concentrations reached during these intervals, ～650–750 ppb, is twice that at the last glacial maximum and is not exceeded until the onset of industrialization at the end of the Holocene. Periods of rapid sea‐level rise as the Last Glacial Maximum ice sheets retreated and associated with ‘melt‐water pulses’ appear to coincide with the onset of elevated concentrations of CH₄, suggestive of a potential causative link. Here we identify and outline a mechanism involving the flooding of the continental shelves that were exposed and vegetated during the glacial sea‐level low stand and that can help account for some of these observations. Specifically, we hypothesize that waterlogging (and later, flooding) of large tracts of forest and savanna in the Tropics and Subtropics during the deglacial transition and early Holocene would have resulted in rapid anaerobic decomposition of standing biomass and emission of methane to the atmosphere. This novel mechanism, akin to the consequences of filling new hydroelectric reservoirs, provides a mechanistic explanation for the apparent synchronicity between rate of sea‐level rise and occurrence of elevated concentrations of ice core CH₄. However, shelf flooding and the creation of transient wetlands are unlikely to explain more than ～60 ppb of the increase in atmospheric CH₄ during the deglacial transition, requiring additional mechanisms to explain the bulk of the glacial to interglacial increase. Similarly, this mechanism has the potential also to play some role in the rapid changes in atmospheric methane associated with the Dansgaard–Oeschger cycles. Copyright © 2012 John Wiley & Sons, Ltd.     

Separating contributions from natural and anthropogenic sources in atmospheric methane from the Black Sea region,Romania

The Danube Delta-Black Sea region of Romania is an important wetland, and this preliminary study evaluates the significance of this region as a source of atmospheric CH₄. Measurements of the mixing ratio and δ¹³C in CH₄ are reported from air and water samples collected at eight sites in the Danube Delta. High mixing ratios of CH₄ were found in air (2500–14,000 ppb) and dissolved in water samples (∼1–10 μmol L⁻¹), demonstrating that the Danube Delta is an important natural source of CH₄. The intercepts on Keeling plots of about −62‰ show that the main source of CH₄ in this region is microbial, probably resulting primarily from acetate fermentation. Atmospheric CH₄ and CO data from the NOAA/ESRL (National Oceanic and Atmospheric Administration/Earth System Research Laboratory) were used to make a preliminary estimate of biogenic CH₄ at the Black Sea sampling site at Constanta (BSC). These data were used to calculate ratios of CH₄/CO in air samples, and using an assumed CH₄/CO anthropogenic emissions ratio of 0.6, fossil fuel emissions at BSC were estimated. Biogenic CH₄ emissions were then estimated by a simple mass balance approach. Keeling plots of well-mixed air from the BSC site suggested a stronger wetland source in summer and a stronger fossil fuel source in winter.     

Methane distribution and cycling in Tomales Bay, California

Cycling of methane (CH₄) in Tomales Bay, a 28-km² temperature estuary in northern California with relatively low inputs of organic carbon, was studied over a 1-yr period. Water column CH₄ concentrations showed spatial and temporal variability (range=8–100 nM), and were supersaturated with respect to the atmosphere by a factor of 2–37. Rates of net water column CH₄ production-oxidation were determined by in situ experiments, and were not found to be significantly different from zero. Fluxes across the sediment-water interface, determined by direct measurement using benthic chambers, varied from ?0.1 μmol m^?2 d^?1 to +16 μmol m^?2 d^?1 (positive fluxes into water). Methane concentrations in the two perennial creeks feeding the bay varied annually (140–950 nM); these creeks were a significant CH₄ source to the bay during winter. In addition, mass-balance calculations indicate a significant additional inter CH₄ source, which is hypothesized to result from storm-related runoff from dairy farms adjacent to the bay. Systemwide CH₄ budgets of the 16-km² inner bay indicate benthic production (110 mol d^?1) and atmospheric evasion (110 mol d^?1) dominated during summer, while atmospheric evasion (160 mol d^?1) and runoff from dairy farms (90 mol d^?1) dominated during winter.     

Atmospheric input of inorganic nitrogen to Delaware Bay

The coastal waters of the mid-Atlantic region of the United States receive inputs of atmospheric pollutants as a consequence of being located downwind from major industrial and urban emissions. These inputs are potentially the largest received by any marine area of the country. Of current interest is the atmospheric input of dissolved inorganic nitrogen (DIN = NO₃ ^?+NH₄ ⁺). We have conducted a first-order examination of the magnitude of atmospheric DIN deposition relative to other large-scale inputs for Delaware Bay, a partially urbanized mid-Atlantic coastal plain estuary. The following loading terms: direct atmospheric deposition, indirect atmospheric loading, urban point discharges, fluvial input, benthic flux, and salt marsh export were evaluated. On an annual basis, municipal-industrial effluents provide a dominant source (ca. 40%) of the DIN inputs to the estuary. Total (wet plus dry) atmospheric deposition accounts for about 15% of the total annual DIN inputs. However, during summer, which is characterized by low river-flow and seasonally maximum atmospheric loading, this figure increases to around 25%. Although atmospheric input can satisfy only a fraction of the primary production demands, this summer flux may represent an ecologically important source of external DIN, half of which is directly deposited to surface photic zones where it is readily available for biological uptake.     

中国农田的温室气体排放

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

Modelling the effects of climate change on methane emission from a northern ombrotrophic bog in Canada

Peatlands are a large potential source of methane (CH₄) to the atmosphere. In order to investigate the effects of climate change on CH₄ emission from northern ombrotrophic peatlands, a simulation model coupling water table dynamics with methane emission was developed for the Mer Bleue Bog in Ontario, Canada. The model was validated against reported values of CH₄ flux from field measurements and the model outputs exhibited high sensitivity to acrotelm thickness, leaf area index, transmissivity and slope of water table. With a 2–4°C temperature rise over the 4-year simulation period, the rate of CH₄ release dropped significantly to under 0.1 mg m⁻² day⁻¹. On the other hand, mean CH₄ emission increased by >26-fold when the increase in precipitation was >15%. When looking at the combined effects, the highest CH₄ release (13.3 mg m⁻² day⁻¹) was attained under the scenario of 2°C temperature rise and 25% precipitation increase. Results obtained in this study highlight the importance of avoiding more extreme climate change, which would otherwise lead to enhanced methane release from peatlands and further atmospheric warming through positive feedback.     

Light hydrocarbons geochemistry of surface sediments from Pranhita-Godavari Basin,Andhra Pradesh

A geochemical study of surface sediments from Pranhita-Godavari Basin, Andhra Pradesh, India was carried out using light hydrocarbon compounds to assess the hydrocarbon potential of the basin. Suite of 80 soil samples were collected from the depth of 2.5 m and analyzed for adsorbed light gaseous hydrocarbons namely methane (CH₄), ethane (C₂H₆) and propane (C₃H₈) in Gas chromatograph. Compound specific Carbon isotope ratios for CH₄ and C₂H₆ were also determined using GC-C IRMS (Gas Chromatograph Combustion Isotope Mass Spectrometer). The presence of moderate to low concentrations of methane (C_CH4 C_{CH_4 } : 1 to 138 ppb), ethane (H₄{H_4 }: 1 to 35 ppb) and propane (C_{C3 H8} C_{C_3 H_8 } : 1 to 20 ppb) was measured in the soil samples. Carbon isotopic composition of d¹³ C_CH4 \delta ^{13} C_{CH_4 } ranges between −27.9 to −47.1 ‰ and d¹³ C_{C2 H6} \delta ^{13} C_{C_2 H_6 } ranged between −36.9 to −37.2 ‰ (V-PDB) indicating that these gases are of thermogenic origin. Study of soil samples suggests the area has good potential for hydrocarbon.     

A Holocene vegetation record from the Mississippi River Valley, southeastern Missouri

Pollen preserved in a peat deposit from a large swamp, the Old Field in the Mississippi River Valley near Advance, Missouri, records radiocarbon-dated vegetation changes between 9000 and about 3000 years ago. The principal feature of both the percentage and influx pollen diagrams is the replacement of arboreal pollen, primarily Quercus, Fraxinus, and Cephalanthus, with Gramineae and NAP between 8700 and 5000 years BP. This vegetation shift is interpreted as reflecting a decrease in the extent of the Old Field swamp and its associated bottomland forest species along with the expansion of a grass-dominated herb community, as a result of a reduction in available ground water. The desiccation of the swamp during this period indicates a reduction in precipitation within the ground-water source area and a shift to a drier climate in the southern Midwest. The pollen suggests that the lowest water levels and driest climate in southeastern Missouri lasted from 8700 to 6500 years BP, at which time there is a partial reappearance of swamp species. Relatively dry conditions, however, continued until at least 5000 years BP. Although pollen influx data are lacking from the upper part of the profile, the relative pollen frequencies suggest an increase in trees after 5000 BP. The replacement of the arboreal vegetation by grasses and herbs between 8700 and 5000 years BP reflects the period of maximum expansion of the Prairie Peninsula in southeastern Missouri. The Old Field swamp provides the first pollen evidence that the vegetational changes along the southern border of the Prairie Peninsula were chronologically similar to those on the northern and northeastern margins.     

Cold climate during the closest Stage 11 analog to recent Millennia

The early part of marine isotopic Stage 11 near 400,000 years ago provides the closest analog to Holocene insolation levels of any interglaciation during the era of strong 100,000-year climatic cycles. The CH₄ concentration measured in Vostok ice fell to ∼450 ppb, and CO₂ values to ∼250 ppm. These natural decreases contrast with the increases in recent millennia and support the early anthropogenic hypothesis of major gas emissions from late-Holocene farming. During the same interval, δD values fell from typical interglacial to nearly glacial values, indicating a major cooling in Antarctica early in Stage 11. Other evidence suggests that new ice was accumulating during the closest insolation analog to the present day: a major increase in δ¹⁸O_atm at Vostok, a similar increase in marine δ¹⁸O values, and re-initiation of ice rafting in the Nordic Sea. The evidence permits extended (>20,000 year) intervals of Stage 11 interglacial warmth in the Antarctic and North Atlantic, yet it also requires that this warmth ended and a new glacial era began when insolation was most similar to recent millennia. The Holocene CO₂ anomaly was produced only in part by direct anthropogenic emissions; over half of the anomaly resulted from the failure of CO₂ values to fall as they had during previous interglaciations because of natural responses, including a sea-ice advance in the Antarctic and ice-sheet growth in the northern hemisphere.     

Orbital insolation,ice volume,and greenhouse gases

The SPECMAP models of orbital-scale climate change (Imbrie et al., Paleoceanography 7 (1992) 701, Paleoceanography 8 (1993) 699) are the most comprehensive to date: all major climatic observations were analyzed within the framework of the three orbital signals. Subsequently, tuning of signals in Vostok ice to insolation forcing has fixed the timing of greenhouse-gas changes closely enough to permit an assessment of their orbital-scale climatic role. In addition, evidence from several sources has suggested changes in the SPECMAP δ¹⁸O time scale. This new information indicates that the timing of CO₂ changes at the periods of precession and obliquity does not fit the 1992 SPECMAP model of a “train” of responses initiated in the north, propagated to the south, and later returning north to force the ice sheets. In addition, analysis of the effects of rectification on 100,000-year climatic signals reveals that all have a phase on or near that of eccentricity. This close clustering of phases rules out the long time constants for 100,000-year ice sheets required by the 1993 SPECMAP model.A new hypotheses presented here revives elements of an earlier CLIMAP view (Hays et al., Science 194 (1976a) 1121) but adds a new assessment of the role of greenhouse gases.As proposed by Milankovitch, summer (mid-July) insolation forces northern hemisphere ice sheets at the obliquity and precession periods, with an ice time constant derived here of 10,000 years. Changes in ice volume at 41,000 years drive ice-proximal signals (SST, NADW, dust) that produce a strong positive CO₂ feedback and further amplify ice-volume changes. At the precession period, July insolation forces ice sheets but it also drives fast and early responses in CH₄ through changes in tropical monsoons and boreal wetlands, and variations in CO₂ through southern hemisphere processes. These CH₄ and CO₂ responses enhance insolation forcing of ice volume.Climatic responses at 100,000 years result from eccentricity pacing of forced processes embedded in obliquity and precession cycles. Increased modulation of precession by eccentricity every 100,000 years produces 23,000-year CO₂ and CH₄ maxima that enhance ablation caused by summer insolation and drive climate deeper into an interglacial state. When eccentricity modulation decreases at the 100,000-year cycle, ice sheets grow larger in response to obliquity forcing and activate a 41,000-year CO₂ feedback that drives climate deeper into a glacial state. Alternation of these forced processes because of eccentricity pacing produces the 100,000-year cycle. The 100,000-year cycle began 0.9 Myr ago because gradual global cooling allowed ice sheets to survive during weak precession insolation maxima and grow large enough during 41,000-year ice-volume maxima to generate strong positive CO₂ feedback.The natural orbital-scale timing of these processes indicates that ice sheets should have appeared 6000–3500 years ago and that CO₂ and CH₄ concentrations should have fallen steadily from 11,000 years ago until now. But new ice did not appear, and CO₂ and CH₄ began anomalous increases at 8000 and 5000 years ago, respectively. Human generation of CO₂ and CH₄ is implicated in these anomalous trends and in the failure of ice sheets to appear in Canada.     

Spaceborne remote sensing of greenhouse gas concentrations

Despite their primary contribution to climate change, there are still large uncertainties on the sources and sinks of the main greenhouse gases: carbon dioxide (CO₂), methane (CH₄) and nitrous oxide (N₂O). A better knowledge of these sources is necessary to understand the processes that control them and therefore to predict their variations. Indeed, large feedbacks between climate change and greenhouse gas fluxes are expected during the 21st century. Sources and sinks of these gases generate spatial and temporal gradients that can be measured either in situ or from space. One can then estimate the surface fluxes, either positive or negative, from concentration measurements through a so-called atmospheric inversion. Surface measurements are currently used to estimate the fluxes at continental scales. The high density of spaceborne observations allows potentially a much higher resolution. Several remote sensing techniques can be used to measure atmospheric concentration of greenhouse gases. These techniques have motivated the development of spaceborne instruments, some of them already in space and others under development. However, the accuracy of the current estimates is still not sufficient to improve our knowledge on the greenhouse gases sources and sinks. Rapid improvements are expected during the forthcoming years with a strong implication of the scientific community and the launch of dedicated instruments, optimized for the measurement of CO₂ and CH₄ concentrations.     

Late Holocene Baltic Sea outflow changes reconstructed using C37:4 content from marine cores

The Baltic Sea is an intra‐continental brackish water body. Low saline surface water, the so‐called Baltic outflow current, exits the Baltic Sea through the Kattegat into the Skagerrak. Ingressions of saline oxygen‐rich bottom water enter the Baltic Sea basins via the narrow and shallow Kattegat and are of great importance for the ecological and ventilation state of the Baltic Sea. Over recent decades, progress has been made in studying Holocene changes in saline water inflow. However, reconstructions of past variations in Baltic Sea outflow changes are sparse and hampered because of the lack of suitable proxies. Here, we used the relative proportion of tetra‐unsaturated C₃₇ ketones (C_37:4 %) in long‐chain alkenones produced by coccolithophorids as a proxy for outflowing Baltic Sea water in the Skagerrak. To evaluate the applicability of the proxy, we compared the biomarker results with grain‐size records from the Kattegat and Mecklenburg Bay in addition to previously published salinity reconstructions from the Kattegat over the last 5000 years. All Skagerrak records showed an increase in C_37:4 % that is accompanied by enhanced bottom water currents in the Kattegat and western Baltic Sea over the past 3500 cal. a BP, indicating an increase in Baltic Sea outflow. This probably reflects higher precipitation in the Baltic Sea catchment area owing to a re‐organization of North Atlantic atmospheric circulation with an increased influence of wintertime Westerlies over the Baltic catchment from the mid‐ to the late Holocene.     

Contribution of a sewage sludge application to the short-term carbon sequestration across a wide range of agricultural soils

The atmospheric levels of carbon dioxide (CO₂) and other greenhouse gases (GHGs) have increased dramatically since the industrial revolution. The atmospheric enrichment with CO₂ and other GHGs has resulted in multiple negative consequences: such as the increase in the average temperature and the rise of the sea level. Hence, there is a growing interest in developing feasible methods to reduce the atmospheric levels of these gases. One of these strategies is to enhance C sequestration through the increase of soil organic carbon (SOC) pool by the amendment of agricultural soils with sewage sludge. However, there is considerable uncertainty about the effects (positive or negative) of sewage sludge applications on the SOC pool. Thus, a simple approach developed under laboratory conditions is presented to discern the effect of a single sewage sludge application of 50 t ha⁻¹ on the short-term SOC pool in 60 contrasting agricultural soils. The role of soil factors in the C sequestration of the recently added carbon was also studied. The application of sewage sludge supposed a mean increase of 1.7 ± 1.6 g SOC kg⁻¹, with peak increases of up to 3.8 g SOC kg⁻¹ and decreases of up to 4.6 g SOC kg⁻¹. The initial SOC contents conditioned the C sequestration after sewage sludge application, and no other soil property was related.     

Late Quaternary palæoecology and palæoclimates of the eastern Sahara

Latest field research and palæoenvironmental reconstructions have revealed that within less than 6000 years the eastern Sahara experienced a dramatic climatic change similar to that in the western Sahara, passing from hyperaridity to semi-aridity (dry savanna) to its present hyperarid state. Groundwater levels started to rise about 9300 years before present (¹⁴C years BP), leading to the formation of a mosaic of freshwater lakes and swamps. Within a few decades, the aquifers were loaded and the palæopiezometric surface was as much as 25 m higher than it is today. The uplands generated up to 800 km long fluvial systems, which put an end to the endorheic drainage of the region and functioned as migration paths for large savanna mammals. These wetter conditions persisted in Western Nubia during the Holocene until ca 5000 years BP The climatic deterioration began around 5700 years BP as shown by evaporitic sediments. Reversal events prior to aridification during the Late Holocene were not recorded systematically in the sediments of the eastern Sahara because of the stability of the ecosystems. Changes in land-surface conditions such as palæolakes, swamps and vegetation created water vapour sources that generated local rainfall and buffered short dry spells. Radiocarbon-dated charcoal indicates that Neolithic human occupation culminated during this Early Holocene wet phase and ended ca 2000 years after the fading of the wet phase at about 3000 years BP, when the shallow aquifers were exhausted.     

Tracing industrial sulfur contributions to atmospheric sulfate deposition in the Athabasca oil sands region,Alberta, Canada

Anthropogenic S emissions in the Athabasca oil sands region (AOSR) in Alberta, Canada, affect SO₄ deposition in close vicinity of industrial emitters. Between May 2008 and May 2009, SO₄-S deposition was monitored using open field bulk collectors at 15 sites and throughfall collectors at 14 sites at distances between 3 and 113 km from one of the major emission stacks in the AOSR. At forested plots >90 km from the operations, SO₄ deposition was ∼1.4 kg SO₄-S ha⁻¹ yr⁻¹ for bulk deposition and ∼3.3 kg SO₄-S ha⁻¹ yr⁻¹ for throughfall deposition. Throughfall SO₄ deposition rates in the AOSR exceeded bulk deposition rates at all sites by a factor of 2–3, indicating significant inputs of dry deposition especially under forest canopies. Both bulk and throughfall SO₄ deposition rates were elevated within 29 km distance of the industrial operations with deposition rates as high as 11.7 kg SO₄-S ha⁻¹ yr⁻¹ for bulk deposition and 39.2 kg SO₄-S ha⁻¹ yr⁻¹ for throughfall at industrial sites. Sulfur isotope ratio measurements of atmospheric SO₄ deposited in the AOSR revealed that at a few selected locations ³⁴S-depleted SO₄, likely derived from H₂S emissions from tailing ponds contributes to local atmospheric SO₄ deposition. In general, however, δ³⁴S values of SO₄ deposition at distant forested plots (>74 km) with low deposition rates were not isotopically different from δ³⁴S values at sites with high deposition rates in the AOSR and are, therefore, not suitable to determine industrial S contributions. However, O isotope ratios of atmospheric SO₄ in bulk and throughfall deposition in the AOSR showed a distinct trend of decreasing δ¹⁸O-SO₄ values with increasing SO₄ deposition rates allowing quantification of industrial contributions to atmospheric SO₄ deposition. Two-end-member mixing calculations revealed that open field bulk SO₄ deposition especially at industrial sites in close proximity (<29 km) to the operations is significantly (17–59%) affected by industrial S emissions and that throughfall generally contained 49–100% SO₄ of industrial origin. Hence, it is suggested that δ¹⁸O values of SO₄ may constitute a suitable tracer for quantifying industrial contributions to atmospheric SO₄ deposition in the AOSR.     

Inferences about winter temperatures and summer rains from the late Quaternary record of C4 perennial grasses and C3 desert shrubs in the northern Chihuahuan Desert

Late Quaternary histories of two North American desert biomes—C₄ grasslands and C₃ shrublands—are poorly known despite their sensitivity and potential value in reconstructing summer rains and winter temperatures. Plant macrofossil assemblages from packrat midden series in the northern Chihuahuan Desert show that C₄ grasses and annuals typical of desert grassland persisted near their present northern limits throughout the last glacial–interglacial cycle. By contrast, key C₃ desert shrubs appeared somewhat abruptly after 5000 cal. yr BP. Bioclimatic envelopes for select C₄ and C₃ species are mapped to interpret the glacial–interglacial persistence of desert grassland and the mid‐to‐late Holocene expansion of desert shrublands. The envelopes suggest relatively warm Pleistocene temperatures with moist summers allowed for persistence of C₄ grasses, whereas winters were probably too cold (or too wet) for C₃ desert shrubs. Contrary to climate model results, core processes associated with the North American Monsoon and moisture transport to the northern Chihuahuan Desert remained intact throughout the last glacial–interglacial cycle. Mid‐latitude effects, however, truncated midsummer (July–August) moisture transport north of 35° N. The sudden expansion of desert shrublands after 5000 cal. yr BP may be a threshold response to warmer winters associated with increasing boreal winter insolation, and enhanced El Niño–Southern Oscillation variability. Published in 2006 by John Wiley & Sons, Ltd.     

Dynamics of greenhouse gases in the river–groundwater interface in a gaining river stretch (Triffoy catchment,Belgium)

This study investigates the occurrence of greenhouse gases (GHGs) and the role of groundwater as an indirect pathway of GHG emissions into surface waters in a gaining stretch of the Triffoy River agricultural catchment (Belgium). To this end, nitrous oxide (N₂O), methane (CH₄) and carbon dioxide (CO₂) concentrations, the stable isotopes of nitrate, and major ions were monitored in river and groundwater over 8 months. Results indicated that groundwater was strongly oversaturated in N₂O and CO₂ with respect to atmospheric equilibrium (50.1 vs. 0.55 μg L^?1 for N₂O and 14,569 vs. 400 ppm for CO₂), but only marginally for CH₄ (0.45 vs. 0.056 μg L^?1), suggesting that groundwater can be a source of these GHGs to the atmosphere. Nitrification seemed to be the main process for the accumulation of N₂O in groundwater. Oxic conditions prevailing in the aquifer were not prone for the accumulation of CH₄. In fact, the emissions of CH₄ from the river were one to two orders of magnitude higher than the inputs from groundwater, meaning that CH₄ emissions from the river were due to CH₄ in-situ production in riverbed or riparian zone sediments. For CO₂ and N₂O, average emissions from groundwater were 1.5?×?10⁵ kg CO₂ ha^?1 year^?1 and 207 kg N₂O ha^?1 year^?1, respectively. Groundwater is probably an important source of N₂O and CO₂ in gaining streams but when the measures are scaled at catchment scale, these fluxes are probably relatively modest. Nevertheless, their quantification would better constrain nitrogen and carbon budgets in natural systems.     

Methane flux from mangrove sediments along the Southwestern coast of Puerto Rico

Although the sediments of coastal marine mangrove forests have been considered a minor source of atmospheric methane, these estimates have been based on sparse data from similar areas. We have gathered evidence that shows that external nutrient and freshwater loading in mangrove sediments may have a significant effect on methane flux. Experiments were performed to examine methane fluxes from anaerobic sediments in a mangrove forest subjected to secondary sewage effluents on the southwestern coast of Puerto Rico. Emission rates were measured in situ using a static chamber technique, and subsequent laboratory analysis of samples was by gas chromatography using a flame ionization detector. Results indicate that methane flux rates were lowest at the landward fringe nearest to the effluent discharge, higher in the seaward fringe occupied by red mangroves, and highest in the transition zone between black and red mangrove communities, with average values of 4 mg CH₄ m^?2 d^?1, 42 mg CH₄ m^?2 d^?1, and 82 mg CH₄ m^?2 d^?1, respectively. Overall mean values show these sediments may emit as much as 40 times more methane than unimpacted pristine areas. Pneumatophores ofAviciennia germinans have been found to serve as conduits to the atmosphere for this gas. Fluctuating water level overlying the mangrove sediment is an important environmental factor controlling seasonal and interannual CH₄ flux variations. Environmental controls such as freshwater inputs and increased nutrient loading influence in situ methane emissions from these environments.     

Thermodynamic modeling of binary CH4-H2O fluid inclusions

This work reports the application of thermodynamic models, including equations of state, to binary (salt-free) CH₄-H₂O fluid inclusions. A general method is presented to calculate the compositions of CH₄-H₂O inclusions using the phase volume fractions and dissolution temperatures of CH₄ hydrate. To calculate the homogenization pressures and isolines of the CH₄-H₂O inclusions, an improved activity-fugacity model is developed to predict the vapor-liquid phase equilibrium. The phase equilibrium model can predict methane solubility in the liquid phase and water content in the vapor phase from 273 to 623 K and from 1 to 1000 bar (up to 2000 bar for the liquid phase), within or close to experimental uncertainties. Compared to reliable experimental phase equilibrium data, the average deviation of the water content in the vapor phase and methane solubility in the liquid phase is 4.29% and 3.63%, respectively. In the near-critical region, the predicted composition deviations increase to over 10%. The vapor-liquid phase equilibrium model together with the updated volumetric model of homogenous (single-phase) CH₄-H₂O fluid mixtures (Mao S., Duan Z., Hu J. and Zhang D. (2010) A model for single-phase PVTx properties of CO₂-CH₄-C₂H₆-N₂-H₂O-NaCl fluid mixtures from 273 to 1273 K and from 1 to 5000 bar. Chem. Geol.275, 148-160), is applied to calculate the isolines, homogenization pressures, homogenization volumes, and isochores at specified homogenization temperatures and compositions. Online calculation is on the website: http://www.geochem-model.org/.     

Methane formation in soil–plant systems treating wastewater as influenced by microbial populations

The present study evaluated the effect of plant species on methane (CH₄) emission and microbial populations in three types of soil–plant systems. Results showed large variation of CH₄ flux rate ranging from 1.35 to 212.61 mg CH₄ m^?2 h^?1. Emission peak of CH₄ occurred in July. No significant difference was found in the non-vegetation system spanning 2 years. Compared with non-vegetation, vegetation systems had much higher flux of CH₄, and obvious seasonal variation was observed. The polyculture system planted with Zizania latifolia (Z. latifolia) and Phragmites australis (P. australis) released higher CH₄ fluxes than the mono system (P. australis), reflecting that Z. latifolia growth could simulate CH₄ emission. The fluorescence in situ hybridization (FISH) results support the characteristics of CH₄ fluxes. Much higher methanotrophs amount and lower methanogens amount from the mono system than those from the polyculture system was observed indicating that Z. latifolia growth may limit the oxygen transportation resulting in higher CH₄ emission. The polyculture system has the highest potential of CH₄ emission.