The Influence of Rewetting on Vegetation Development and Decomposition in a Degraded Fen

The rewetting technique border irrigation was installed in a degraded fen peatland in northeastern Germany. Because of the prevailing site conditions, the technique resulted in two different rewetting variants (surface irrigation and temporary inundation) at the study site. This paper reports on the practicability of this technique and the influence of rewetting on vegetation development, decomposition processes and soil nutrient availability, and the possibilities for renewed peat accumulation. The technique proved to be suited for rewetting fen sites with a continuous slope, deep peat layer with low hydraulic conductivity, and upstream water recharge facilities. A subsidence of the ground‐water levels during the summer months, however, could not be avoided in dry years. The vegetation changed slowly from species‐poor grassland into typical fen plant communities, despite rewetting and soil tillage. Species richness, however, was higher in the surface irrigation than in the temporary inundation variant. A sufficient water supply proved to be absolutely necessary to retard decomposition processes because higher decomposition of root materials (i.e., higher k values) occurred under temporary inundated conditions. Generally, the higher water content in the soil after rewetting led to a lower nitrate‐N–to–ammonium‐N ratio in the topsoil in both rewetting variants. In the surface irrigation variant the mineral nitrogen content (Nmin) of the topsoil decreased from 7.8 to 4.4 g N/m², which is also correlated with the increase in water content of the soil. The low Nmin levels of fens which were never deeply drained (0.9–2.8 g N/m²), however, were not reached within the observation period of 3 years.     

Restoration of peat‐forming vegetation by rewetting species‐poor fen grasslands

Questions: Does succession of rewetted species‐poor fen grasslands display similar trends when different water levels, sites and regions are compared? Will restoration targets as peat growth and waterfowl diversity be reached? Location: Valley fen of the river Peene (NE‐Germany) and the Hanság fen (Lake Neusiedler See, NW‐Hungary). Methods: Analysis of permanent plot data and vegetation maps over a period of up to seven years of rewetting. The general relations between newly adjusted water levels and changes in dominance of helophytic key species during early succession are analysed considering four rewetting intensities (water level classes) and eight vegetation types (Phalaris arundinacea type, Carex type, Glyceria maxima type, Phragmites australis type, Typha type, aquatic vegetation type, open water type and miscellaneous type). Results: The initial period of balancing the site conditions and vegetation is characterised by specific vegetation types and related horizontal vegetation structures. Most vegetation types displayed similar trends within the same water level class when different sites and regions were compared. A significant spread of potentially peat forming vegetation with dominance of Carex spp. or Phragmites as desired goal of restoration was predominantly restricted to long‐term shallow inundated sites (water level median in winter: 0–30 cm above surface). Open water patches as bird habitats persisted mainly at permanent inundated sites (water level median in winter > 60 cm above surface). Conclusions: Site hydrology appeared as a main force of secondary succession. Thus the rewetting intensity and restoration targets have to be balanced adequately.     

Vegetation controls methane emissions in a coastal brackish fen

Climate change and associated sea level rise will likely affect coastal ecosystems and lead to more frequent inundations. Plants are an important control for methane (CH₄) emissions in peatlands because the metabolism of the living plant can either enhance or attenuate CH₄ emissions and plant litter supplies an easily available carbon source for methanogenesis. Here we compare the contribution of various dominant plant species to methane emissions in a degraded, rewetted coastal brackish fen at the southern Baltic Sea coast in Northeast Germany. We analyse one year of bi-weekly static closed chamber data gathered at measurement spots that were located in different mono-dominant vegetation stands (Bolboschoenus maritimus (L.) Palla, Schoenoplectus tabernaemontani (C.C.Gmel.) Palla, Carex acutiformis Ehrh.). Furthermore, data on water level, water temperature, conductivity (sulphate), and several peat characteristics were recorded. Generally, the annual methane emissions were low with an average across vegetation stands of 14 kg CH₄ ha^?1 a^?1, which we related to high decomposition of peat after drainage and to relatively low water levels in summer. Nevertheless, methane emissions varied between different vegetation types with significantly higher methane fluxes (31.8 ± 5.7 kg CH₄ ha^?1 a^?1) from Bolboschoenus maritimus stands compared to Carex acutiformis and Schoenoplectus tabernaemontani stands (4.3 ± 1.2 and 5.7 ± 2.4 kg CH₄ ha^?1 a^?1, respectively). None of the environmental variables that have been recorded can explain this difference. Thus, vegetation composition seems to be an important driver for methane emissions in coastal brackish fens and may therefore be crucial with regard to recreation measures.     

Assessing greenhouse gas emissions from peatlands using vegetation as a proxy

Drained peatlands in temperate Europe are a globally important source of greenhouse gas (GHG) emissions. This article outlines a methodology to assess emissions and emission reductions from peatland rewetting projects using vegetation as a proxy. Vegetation seems well qualified for indicating GHG fluxes from peat soils as it reflects long-term water level, affects GHG emissions via assimilate supply and aerenchyma and allows fine-scaled mapping. The methodology includes mapping of vegetation types characterised by the presence and absence of species groups indicative for specific water level classes. GHG flux values are assigned to the vegetation types following a standardized protocol and using published emission values from plots with similar vegetation and water level in regions with similar climate and flora. Carbon sequestration in trees is accounted for by estimating the annual sequestration in tree biomass from forest inventory data. The method follows the criteria of the Voluntary Carbon Standard and is illustrated using the example of two Belarusian peatlands.     

Land use of drained peatlands: Greenhouse gas fluxes,plant production,and economics

Drained peatlands are hotspots for greenhouse gas (GHG) emissions, which could be mitigated by rewetting and land use change. We performed an ecological/economic analysis of rewetting drained fertile peatlands in a hemiboreal climate using different land use strategies over 80 years. Vegetation, soil processes, and total GHG emissions were modeled using the CoupModel for four scenarios: (1) business as usual—Norway spruce with average soil water table of ?40 cm; (2) willow with groundwater at ?20 cm; (3) reed canary grass with groundwater at ?10 cm; and (4) a fully rewetted peatland. The predictions were based on previous model calibrations with several high‐resolution datasets consisting of water, heat, carbon, and nitrogen cycling. Spruce growth was calibrated by tree‐ring data that extended the time period covered. The GHG balance of four scenarios, including vegetation and soil, were 4.7, 7.1, 9.1, and 6.2 Mg CO₂eq ha^?1 year^?1, respectively. The total soil emissions (including litter and peat respiration CO₂ + N₂O + CH₄) were 33.1, 19.3, 15.3, and 11.0 Mg CO₂eq ha^?1 year^?1, respectively, of which the peat loss contributed 35%, 24%, and 7% of the soil emissions for the three drained scenarios, respectively. No peat was lost for the wet peatland. It was also found that draining increases vegetation growth, but not as drastically as peat respiration does. The cost–benefit analysis (CBA) is sensitive to time frame, discount rate, and carbon price. Our results indicate that the net benefit was greater with a somewhat higher soil water table and when the peatland was vegetated with willow and reed canary grass (Scenarios 2 and 3). We conclude that saving peat and avoiding methane release using fairly wet conditions can significantly reduce GHG emissions, and that this strategy should be considered for land use planning and policy‐making.     

Functional-Structural Analysis of Nitrogen-Cycle Bacteria in a Hypersaline Mat from the Omani Desert

Anaerobic microbial activity in northern peat soils most often results in more carbon dioxide (CO ₂ ) production than methane (CH₄) production. This study examined why methanogenic conditions (i.e., equal molar amounts of CH₄ production and CO₂ production) prevail so infrequently. We used peat soils from two ombrotrophic bogs and from two rheotrophic fens. The former two represented a relatively dry bog hummock and a wet bog hollow, and the latter two represented a forested fen and a sedge-dominated fen. We quantified gas production rates in soil samples incubated in vitro with and without added metabolic substrates (glucose, ethanol, H₂/CO₂). None of the peat soils exhibited methanogenic conditions when incubated in vitro for a short time (< 5 days) and without added substrates. Incubating some samples > 50 days without added substrates led to methanogenic conditions in only one of four experiments. The anaerobic CO₂:CH₄ production ratio ranged from 5:1 to 40:1 in peat soil without additions and was larger in samples from the dry bog hummock and forested fen than the wet bog hollow and sedge fen. Adding ethanol or glucose separately to peat soils led to methanogenic conditions within 5 days after the addition by stimulating rates of CH₄ production, suggesting CH₄ production from both hydrogenotrophic and acetoclastic methanogenesis. Our results suggest that methanogenic conditions in peat soils rely on a constant supply of easily decomposable metabolic substrates. Sample handling and incubation procedures might obscure methanogenic conditions in peat soil incubated in vitro.     

Full carbon and greenhouse gas balances of fertilized and nonfertilized reed canary grass cultivations on an abandoned peat extraction area in a dry year

Bioenergy crop cultivation on former peat extraction areas is a potential after‐use option that provides a source of renewable energy while mitigating climate change through enhanced carbon (C) sequestration. This study investigated the full C and greenhouse gas (GHG) balances of fertilized (RCG‐F) and nonfertilized (RCG‐C) reed canary grass (RCG; Phalaris arundinacea) cultivation compared to bare peat (BP) soil within an abandoned peat extraction area in western Estonia during a dry year. Vegetation sampling, static chamber and lysimeter measurements were carried out to estimate above‐ and belowground biomass production and allocation, fluxes of carbon dioxide (CO₂), methane (CH₄) and nitrous oxide (N₂O) in cultivated strips and drainage ditches as well as the dissolved organic carbon (DOC) export, respectively. Heterotrophic respiration was determined from vegetation‐free trenched plots. Fertilization increased the above‐ to belowground biomass production ratio and the autotrophic to heterotrophic respiration ratio. The full C balance (incl. CO₂, CH₄ and DOC fluxes from strips and ditches) was 96, 215 and 180 g C m^?2 yr^?1 in RCG‐F, RCG‐C and BP, respectively, suggesting that all treatments acted as C sources during the dry year. The C balance was driven by variations in the net CO₂ exchange, whereas the combined contribution of CH₄ and DOC fluxes was <5%. The GHG balances were 3.6, 7.9 and 6.6 t CO₂ eq ha^?1 yr^?1 in RCG‐F, RCG‐C and BP, respectively. The CO₂ exchange was also the dominant component of the GHG balance, while the contributions of CH₄ and N₂O were <1% and 1–6%, respectively. Overall, this study suggests that maximizing plant growth and the associated CO₂ uptake through adequate water and nutrient supply is a key prerequisite for ensuring sustainable high yields and climate benefits in RCG cultivations established on organic soils following drainage and peat extraction.     

A synthesis of methane emissions from 71 northern,temperate, and subtropical wetlands

Wetlands are the largest natural source of atmospheric methane. Here, we assess controls on methane flux using a database of approximately 19 000 instantaneous measurements from 71 wetland sites located across subtropical, temperate, and northern high latitude regions. Our analyses confirm general controls on wetland methane emissions from soil temperature, water table, and vegetation, but also show that these relationships are modified depending on wetland type (bog, fen, or swamp), region (subarctic to temperate), and disturbance. Fen methane flux was more sensitive to vegetation and less sensitive to temperature than bog or swamp fluxes. The optimal water table for methane flux was consistently below the peat surface in bogs, close to the peat surface in poor fens, and above the peat surface in rich fens. However, the largest flux in bogs occurred when dry 30‐day averaged antecedent conditions were followed by wet conditions, while in fens and swamps, the largest flux occurred when both 30‐day averaged antecedent and current conditions were wet. Drained wetlands exhibited distinct characteristics, e.g. the absence of large flux following wet and warm conditions, suggesting that the same functional relationships between methane flux and environmental conditions cannot be used across pristine and disturbed wetlands. Together, our results suggest that water table and temperature are dominant controls on methane flux in pristine bogs and swamps, while other processes, such as vascular transport in pristine fens, have the potential to partially override the effect of these controls in other wetland types. Because wetland types vary in methane emissions and have distinct controls, these ecosystems need to be considered separately to yield reliable estimates of global wetland methane release.     

Long‐term effects of drainage and initial effects of hydrological restoration on rich fen vegetation

Questions: What vegetational changes does a boreal rich fen (alkaline fen) undergo during a time period of 24 years after drainage? How is plant species richness affected, and what are the changes in composition of ecological groups of species? Is it possible to recover parts of the original flora by rewetting the rich fen? Which are the initial vegetation changes in the flora after rewetting? What are the major challenges for restoration of rich fen flora after rewetting? Location: Eastern central Sweden, southern boreal vegetational zone. Previously rich fen site, drained for forestry purposes during 1978–1979. The site was hydrologically restored (rewetted) in 2002. Method: Annual vegetation survey in permanent plots during a period of 28 years. Results: There were three successional stages in the vegetational changes. In the first stage there was a rapid (< 5 years) loss of rich fen bryophytes. The second step was an increase of sedges and early successional bryophytes, which was followed by an increase of a few emerging dominants, such as Molinia caerulea, Betula pubescens and Sphagnum spp. After rewetting, there are indications of vegetation recovery, albeit at slow rates. Depending on, for instance, initial species composition different routes of vegetation change were observed in the flora after drainage, although after 24 years, species composition became more homogenous and dominated by a few species with high cover. Conclusion: Major changes have occurred after changes in the hydrology (drainage and rewetting) with a severe impact on the biodiversity among vascular plants and bryophytes. Several rich fen bryophytes respond quickly to the changes in water level (in contrast to vascular plants). The recovery after rewetting towards the original rich fen vegetation is slow, as delayed by substrate degradation, dispersal limitation and presence of dominant species.     

Key variables controlling the vegetation of a cool-temperate mire in northern Japan

Abstract. In the cool-temperate Bibi Mire, Hokkaido, Japan, valley fens and flood-plain fens have quite different vegetation. The main variables controlling the vegetation were all hydrological: mean water level, water level fluctuation and surface water flow. Chemical factors such as electrical conductivity, dissolved oxygen and related peat decomposition were less important. The pH was about neutral and has little effect. The flood-plain fen developed under fluctuating water table conditions. The dominant species are Calamagrostis langsdotffii and Carex pseudocuraica. When temporal inundation occurs in the rainy or typhoon seasons, the submergence stimulates bud germination of the stoloniferous C. pseudocuraica, which can rapidly elongate its stolons upward. Some large floating peat mats occurred in the flood-plain fen zone. On these mats some Alnus japonica saplings establish and patches of alder forest can arise. Here the water level was higher than in the peripheral alder forest zone. The valley fen is dominated by Carex lasiocarpa var. occultans and/or C. limosa. It is formed under stable water table conditions in the inundated parts of the mire -where the non-inundated wet areas are dominated by alder trees. In the area where the surface water is flowing, these two fen sedges grow in deeper water since the high oxygen content is considered to compensate the flooding stress.     

Where old meets new: An ecosystem study of methanogenesis in a reflooded agricultural peatland

Reflooding formerly drained peatlands has been proposed as a means to reduce losses of organic matter and sequester soil carbon for climate change mitigation, but a renewal of high methane emissions has been reported for these ecosystems, offsetting mitigation potential. Our ability to interpret observed methane fluxes in reflooded peatlands and make predictions about future flux trends is limited due to a lack of detailed studies of methanogenic processes. In this study we investigate methanogenesis in a reflooded agricultural peatland in the Sacramento Delta, California. We use the stable‐and radio‐carbon isotopic signatures of wetland sediment methane, ecosystem‐scale eddy covariance flux observations, and laboratory incubation experiments, to identify which carbon sources and methanogenic production pathways fuel methanogenesis and how these processes are affected by vegetation and seasonality. We found that the old peat contribution to annual methane emissions was large (~30%) compared to intact wetlands, indicating a biogeochemical legacy of drainage. However, fresh carbon and the acetoclastic pathway still accounted for the majority of methanogenesis throughout the year. Although temperature sensitivities for bulk peat methanogenesis were similar between open‐water (Q₁₀ = 2.1) and vegetated (Q₁₀ = 2.3) soils, methane production from both fresh and old carbon sources showed pronounced seasonality in vegetated zones. We conclude that high methane emissions in restored wetlands constitute a biogeochemical trade‐off with contemporary carbon uptake, given that methane efflux is fueled primarily by fresh carbon inputs.     

Water mites as potential long-term bioindicators in formerly drained and rewetted raised bogs

Many environmental studies of restored peatlands focus on biogeochemical cycles, productivity and decomposition. However, changes in the composition and structure of invertebrate assemblages in restored bogs have received little attention. In the present study we describe effects of rewetting on the water mite faunas (Acari: Hydrachnidia) of four raised bogs located in northwestern Germany. All examined peatlands had been drained in the past, and two of them had been subjected to peat extraction. The examined sites had been rewetted 2, 12, 14 and 25 years prior to our surveys, and currently represent different stages of plant succession. With increasing age after rewetting, the vegetation developed more complex structure as defined by Sphagnum status, and water mite fauna became somewhat similar to the fauna in an undisturbed raised reference bog. Water mites were found almost exclusively in bogs 25 years after wetting, and in these bogs they occurred in sites with more complex vegetation structure. Because water mites have high demands on abiotic and biotic factors due to their complex life cycle (i.e., the larvae are parasites, and the nymphs and adults are predators), we can infer that their mere presence irrespective of species abundance and richness reflects positive effects of the rewetting measures conducted in peat bogs.     

Flooding and groundwater dynamics in fens in eastern Poland

Abstract. Dynamics in hydrology and water chemistry in the Biebrza mires (Poland) were examined by means of a sampling survey that was repeated four times between 1987 and 1992. The dynamics in the vertical stratigraphy of water types in the peat profile are considerable from close to the mire surface to a depth of 50 cm. Water composition in the root zone correlated best with vegetation types during extremely dry or wet conditions. In the root zone of groundwater-fed rich fens with Caricetum limoso-diandrae and Calamagrostietum strictae vegetation, specific groundwater types evolve from the interaction of discharging groundwater from below the root zone and the temporal influence of precipitation and evapotranspiration. The Caricetum limoso-diandrae is fed by the continuous discharge of nutrient-poor, relatively mineral-rich water. The site conditions in the Calamagrostietum strictae are determined by occasional flooding and the presence of discharging mineral-poor groundwater in the lower part of the root zone. In the Caricetum limoso-diandrae and the Calamagrostietum strictae the maximum variations in water level were 56 and 86 cm, respectively. The composition of shallow groundwater of the Betuletum humilis/Caricetum rostratodiandrae fen is diluted most compared to other vegetation types by rainwater in wet periods. In periods of prolonged drought it has a water type that is affected by evapotranspiration and peat mineralisation. The water level varies by only 33 cm. In the Magnocaricion and Glycerietum maximae in the floodplain the water composition is determined by spring flooding of the river and the natural draw-down that occurs in the following summer. Here, maximum variations in water level were 108 and 117 cm, respectively.     

The role of vegetation in methane flux to the atmosphere: should vegetation be included as a distinct category in the global methane budget?

Currently, the global annual flux of methane (CH₄) to the atmosphere is fairly well constrained at ca. 645 Tg CH₄ year^?1. However, the relative magnitudes of the fluxes generated from different natural (e.g. wetlands, deep seepage, hydrates, ocean sediments) and anthropogenic sources remain poorly resolved. Of the identified natural sources, the contribution of vegetation to the global methane budget is arguably the least well understood. Historically, reviews of the contribution of vegetation to the global methane flux have focused on the role of plants as conduits for soil-borne methane emissions from wetlands, or the aerobic production of methane within plant tissues. Many recent global budgets only include the latter pathway (aerobic methane production) in estimating the importance of terrestrial vegetation to atmospheric CH₄ flux. However, recent experimental evidence suggests several novel pathways through which vegetation can contribute to the flux of this globally important, trace greenhouse gas (GHG), such as plant cisterns that act as cryptic wetlands, heartwood rot in trees, the degradation of coarse woody debris and litter, or methane transport through herbaceous and woody plants. Herein, we synthesize the existing literature to provide a comprehensive estimate of the role of modern vegetation in the global methane budget. This first, albeit uncertain, estimate indicates that vegetation may represent up to 22 % of the annual flux of methane to the atmosphere, contributing ca. 32–143 Tg CH₄ year^?1 to the global flux of this important trace GHG. Overall, our findings emphasize the need to better resolve the role of vegetation in the biogeochemical cycling of methane as an important component of closing the gap in the global methane budget.     

Methane dynamics of recolonized cutover minerotrophic peatland: Implications for restoration

In North America, mulching of vacuum-harvested sites combined with blocking of the drainage system is widely used for peatland restoration to accelerate Sphagnum establishment. However, peat extraction in fen peatlands or exposure of deeper minerotrophic peat layers results in soil chemistry that is less suitable for re-establishment of Sphagnum moss. In this situation, restoration of plant species characteristic of minerotrophic peatlands is desirable to return the site to a carbon accumulating system. In these cases, it may be worthwhile to maintain spontaneously revegetating species as part of restoration if they provide desirable ecosystem functions. We studied the role of six spontaneously recolonizing vegetation communities for methane (CH₄) emissions and pore water CH₄ concentration for two growing seasons (2008 and 2009) at an abandoned minerotrophic peatland in southeastern Quebec. We then compared the results with bare peat and adjacent natural fen vegetation. Communities dominated by Eriophorum vaginatum, Carex aquatilis and Typha latifolia had CH₄ flux an order of magnitude greater than other cutover vegetation types and natural sites. In contrast, Scirpus atrocinctus and Equisetum arvense had CH₄ emission rates lower than natural hollow vegetation. We found seasonal average water table and vegetation volume had significant correlation with CH₄ flux. Water table and soil temperature were significantly correlated with CH₄ flux at plots where the water table was near or above the surface. Pore water CH₄ concentration suggests that CH₄ is being produced at the cutover peatland and that low measured fluxes likely result from substantial oxidation of CH₄ in the unsaturated zone. Understanding ecosystem functions of spontaneously recolonizing species on cutover fens can be used to help make decisions about the inclusion of these communities for future restoration measures.     

Hydro-ecological analysis of the Biebrza mire (Poland)

Vegetation composition and structure of 58 sites along gradients in the valley mire of Biebrza, Poland, are related to physical and chemical variables of groundwater and peat. The three most prominent hydrochemical processes in the valley are (a) dissolution of calcite; (b) dissolution of iron, manganese and aluminium; and (c) enrichment with nitrogen and potassium. Major factors determining these processes are vertical flow of the groundwater and river flooding.Within the rheophilous zone of the mire, calcium-richness of the shallow groundwater and base-saturation of the peat are caused by upward seepage of groundwater originating from adjacent higher grounds. This groundwater movement keeps the larger part of the mire saturated with calcium.Good correlations exist between hydrochemistry and vegetation patterns. Groundwater-fed sites support a characteristic rich fen vegetation (Caricetum limoso-diandrae) with a low biomass production. The flood-plain vegetation consists of highly-productive communities of Glycerietum maximae and Caricetum elatae. In a belt in the Upper Basin where neither flooding nor upward seepage occurs, succession, probably caused by intensified drainage, leads to a dwarf-shrub vegetation (Betuletum humilis; poor fen).     

Nutrient supply in undrained and drained Calthion meadows

Abstract. Plant species-rich Calthion meadows on mesotrophic fen peat soil extensively cut for hay are among the endangered semi-natural vegetation types in northwestern Europe. They are often badly affected by lowering the groundwater table (drainage) and fertilization. In a comparative study of an undrained site with a Calthion meadow and an adjacent drained site, availability of N, P and K was biologically assessed under field conditions (for two years) as well as in a greenhouse (for 18 weeks) by measuring shoot responsiveness. Also, experimental wetting of intact turf samples taken from both sites was applied in order to study the interaction between nutrient supply and anaerobic soil conditions. It was concluded that the above-ground phytomass yield in the undrained site was restricted by a major shortage of N-supply and a moderate shortage of K-supply by the fen peat soil. The above-ground phytomass yield of the drained site was only reduced by a strongly limited supply of K by the soil. The extent of K-deficiency was larger for the drained site. No P-deficiency was observed in any of the drained or undrained sites. Rewetting turf samples, taken from the drained site, did not change above-ground phytomass yields, suggesting that nutrient supplies were not affected by rewetting. Leaching has likely resulted in a strong reduction of K-supply in the drained site. It is assumed that a shortage in K-supply from the peat soil may have become an important environmental constraint for characteristic plant species of Calthion meadows. This may hamper the development of this meadow type on drained peat soils after rewetting by groundwater discharge.     

The importance of floating peat to methane fluxes from flooded peatlands

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.     

Carbon balance and radiative forcing of Finnish peatlands 1900–2100 – the impact of forestry drainage

Natural peatlands accumulate carbon (C) and nitrogen (N). They affect the global climate by binding carbon dioxide (CO₂) and releasing methane (CH₄) to the atmosphere; in contrast fluxes of nitrous oxide (N₂O) in natural peatlands are insignificant. Changes in drainage associated with forestry alter these greenhouse gas (GHG) fluxes and thus the radiative forcing (RF) of peatlands. In this paper, changes in peat and tree stand C stores, GHG fluxes and the consequent RF of Finnish undisturbed and forestry‐drained peatlands are estimated for 1900–2100. The C store in peat is estimated at 5.5 Pg in 1950. The rate of C sequestration into peat has increased from 2.2 Tg a^‐‐1 in 1900, when all peatlands were undrained, to 3.6 Tg a^‐‐1 at present, when c. 60% of peatlands have been drained for forestry. The C store in tree stands has increased from 60 to 170 Tg during the 20th century. Methane emissions have decreased from an estimated 1.0–0.5 Tg CH₄‐‐C a^‐‐1, while those of N₂O have increased from 0.0003 to 0.005 Tg N₂O‐‐N a^‐‐1. The altered exchange rates of GHG gases since 1900 have decreased the RF of peatlands in Finland by about 3 mW m^‐‐2 from the predrainage situation. This result contradicts the common hypothesis that drainage results in increased C emissions and therefore increased RF of peatlands. The negative radiative forcing due to drainage is caused by increases in CO₂ sequestration in peat (‐‐0.5 mW m^‐‐2), tree stands and wood products (‐‐0.8 mW m^‐‐2), decreases in CH₄ emissions from peat to the atmosphere (‐‐1.6 mW m^‐‐2), and only a small increase in N₂O emissions (+0.1 mW m^‐‐2). Although the calculations presented include many uncertainties, the above results are considered qualitatively reliable and may be expected to be valid also for Scandinavian countries and Russia, where most forestry‐drained peatlands occur outside Finland.     

CH4 production and oxidation processes in a boreal fen ecosystem after long‐term water table drawdown

Fens, which extend over vast areas in the Northern hemisphere, are sources of the greenhouse gas CH₄. Climate change scenarios predict a lowering water table (WT) in mires. To study the effect of WT drawdown on CH₄ dynamics in a fen ecosystem, we took advantage of a WT drawdown gradient near a ground water extraction plant. Methane fluxes and CH₄ production and oxidation potentials were related to microbial communities responsible for the processes in four mire locations (wet, semiwet, semidry, and dry). Principal component analyses performed on the vegetation, pH, CH₄, and WT results clearly separated the four sampling locations in the gradient. Long‐term lowering of WT was associated with decreased coverage of Sphagnum and aerenchymatic plants, decreased CH₄ field emissions and CH₄ production potential. Based on mcrA terminal restriction fragment length polymorphism the methanogen community structure correlated best with the methane production and coverage of aerenchymatic plants along the gradient. Methanosarcinaceae and Methanocellales were found at the pristine wet end of the gradient, whereas the Fen cluster characterized the dry end. The methane‐oxidizing bacterial community consisted exclusively of Methylocystis bacteria, but interestingly of five different alleles (T, S, R, M, and O) of the particulate methane monooxygenase marker gene pmoA. The M allele was dominant in the wet locations, and the occurrence of alleles O, S, and T increased with drainage. The occurrence of the R allele that characterized the upper peat layer correlated with CH₄ oxidation potential. These results advance our understanding of mire dynamics after long‐term WT drawdown and of the microbiological bases of methane emissions from mires.