Restoration of Sphagnum and restiad peatlands in Australia and New Zealand reveals similar approaches

Peatlands in Australia and New Zealand are composed mainly of Restionaceous and Cyperaceous peats, although Sphagnum peat is common in wetter climates (Mean Annual Precipitation > 1,000 mm) and at higher altitudes (>1,000 m). Experimental trials in two contrasting peatland types—fire‐damaged Sphagnum peatlands in the Australian Alps and cutover restiad bogs in lowland New Zealand—revealed similar approaches to peatland restoration. Hydrological restoration and rehydration of drying peats involved blocking drainage ditches to raise water tables or, additionally in burnt Sphagnum peatlands, peat‐trenching, and the use of sterilized straw bales to form semipermanent “dam walls” and barriers to spread and slow surface water movement. Recovery to the predisturbance vegetation community was most successful once protective microclimates had been established, either artificially or naturally. Specifically, horizontally laid shadecloth resulted in Sphagnum cristatum regeneration rates and biomass production 3–4 times that of unshaded vegetation (Australia), and early successional nurse shrubs facilitated establishment of Sporadanthus ferrugineus (New Zealand) within 2–3 years. On severely burnt or cutover sites, a patch dynamic approach using transplants of Sphagnum or creation of restiad peat “islands” markedly improved vegetation recovery. In New Zealand, this approach has been scaled up to whole mine‐site restoration, in which the newly vegetated islands provide habitat and seed sources for plants and invertebrates to spread onto surrounding areas. Although a vegetation cover can be established relatively rapidly in both peatland types, restoration of invertebrate communities, ecosystem processes, and peat hydrological function and accumulation may take many decades.     

Change in fluxes of carbon dioxide,methane and nitrous oxide due to forest drainage of mire sites of different trophy

Northern peatlands accumulate atmospheric CO₂ thus counteracting climate warming. However, CH₄ which is more efficient as a greenhouse gas than CO₂, is produced in the anaerobic decomposition processes in peat. When peatlands are taken for forestry their water table is lowered by ditching. We studied long-term effects of lowered water table on the development of vegetation and the annual emissions of CO₂, CH₄ and N₂O in an ombrotrophic bog and in a minerotrophic fen in Finland. Reclamation of the peat sites for forestry had changed the composition and coverage of the field and ground layer species, and increased highly the growth of tree stand at the drained fen. In general, drainage increased the annual CO₂ emissions but the emissions were also affected by the natural fluctuations of water table. In contrast to CO₂, drainage had decreased the emissions of CH₄, the drained fen even consumed atmospheric CH₄. CO₂ and CH₄ emissions were higher in the virgin fen than in the virgin bog. There were no N₂O emissions from neither type of virgin sites. Drainage had, however, highly increased the N₂O emissions from the fen. The results suggest that post-drainage changes in gas fluxes depend on the trophy of the original mires.     

A Multi-Year Record of Methane Flux at the Mer Bleue Bog,Southern Canada

The Mer Bleue peatland is a large ombrotrophic bog with hummock-lawn microtopography, poor fen sections and beaver ponds at the margin. Average growing-season (May–October) fluxes of methane (CH₄) measured in 2002–2003 across the bog ranged from less than 5 mg m⁻² d⁻¹ in hummocks, to greater than 100 mg m⁻² d⁻¹ in lawns and ponds. The average position of the water table explained about half of the variation in the season average CH₄ fluxes, similar to that observed in many other peatlands in Canada and elsewhere. The flux varied most when the water table position ranged between −15 and −40 cm. To better establish the factors that influence this variability, we measured CH₄ flux at approximately weekly intervals from May to November for 5 years (2004–2008) at 12 collars representing the water table and vegetation variations typical of the peatland. Over the snow-free season, peat temperature is the dominant correlate and the difference among the collars’ seasonal average CH₄ flux is partially dependent on water table position. A third important correlate on CH₄ flux is vegetation, particularly the presence of Eriophorum vaginatum, which increases CH₄ flux, as well as differences in the potential of the peat profile to produce and consume CH₄ under anaerobic and aerobic conditions. The combination of peat temperature and water table position with vegetation cover was able to explain approximately 44% of the variation in daily CH₄ flux, based on 1097 individual measurements. There was considerable inter-annual variation in fluxes, associated with varying peat thermal and water table regimes in response to variations in weather, but also by variations in the water level in peripheral ponds, associated with beaver dam activity. Raised water level in the beaver ponds led to higher water tables and increased CH₄ emission in the peatland.     

Initiation of microtopography in revegetated cutover peatlands

Question: How many years are required for a gradient of microtopography to be initiated in revegetated cutover peatlands and become similar to natural bogs? Location: Newly formed Sphagnum carpets on cutover peatlands that revegetated spontaneously after site abandonment (in Estonia), or following active restoration (in Canada) and on undisturbed natural bogs nearby. Methods: Moss surface height was measured along linear transects above a local reference level (the lowest point for a given transect). Heights of at least 20 cm were associated with hummocks. Frequency distributions of surface height and principal component analyses (separately for Canada and Estonia) were conducted to follow the evolution of microtopography in revegetated sites and their similarity with those of natural peatlands. In Canada, regressions were also performed to estimate the time required for the microtopography in revegetated cutover peatlands to become similar to that found in natural bogs. Results: Only 10–30 yr were needed for microstructures comparable to those in natural bogs to develop on restored peatlands where Sphagnum diaspores have been reintroduced. However, this process may take more than a century in cutover peatlands left to revegetate spontaneously. Conclusions: In cutover peatlands with spontaneous revegetation, hummock–hollow formation starts on bare peat which lacks both plant propagules and viable seed banks, and the initiation of microstructures is probably more akin to the process that occurs naturally. Nonetheless, hummock–hollow microtopography resembling that found in natural bogs without pools appeared, in all of the examined cutover peatlands, over periods that are short in terms of peatland development time‐scales. Active peatland restoration could effectively reduce the time required for initiation of microtopography by about 70 yr.     

Effect of water table drawdown on peatland nutrient dynamics: implications for climate change

It is anticipated that a lowering of the water table and reduced soil moisture levels in peatlands may increase peat decomposition rates and consequently affect nutrient availability. However, it is not clear if patterns will be consistent across different peatland types or within peatlands given the natural range of ecohydrological conditions within these systems. We examined the effect of persistent drought on peatland nutrient dynamics by quantifying the effects of an experimentally lowered water table position (drained for a 10-year period) on peat KCl-extractable total inorganic nitrogen (ext-TIN), peat KCl-extractable nitrate (ext-NO₃ ^?), and water-extractable ortho-phosphorus (ext-PO₄ ^3?) concentrations and net phosphorus (P) and nitrogen (N) mineralization and nitrification rates at natural (control) and drained microforms (hummocks, lawns) of a bog and poor fen near Québec City, Canada. Drainage (water table drawdown) decreased net nitrification rates across the landscape and increased ext-NO₃ ^? concentrations, but did not affect net N and P mineralization rates or ext-TIN and ext-PO₄ ^3? concentrations. We suggest that the thick capillary fringe at the drained peatland likely maintained sufficient moisture above the water table to limit the effects of drainage on microbial activity, and a 20 cm lowering of the water table does not appear to have been sufficient to create a clear difference in nutrient dynamics in this peatland landscape. We found some evidence of differences in nutrient concentrations with microforms, where concentrations were greater in lawn than hummock microforms at control sites indicating some translocation of nutrients. In general, the same microtopographic differences were not observed at drained sites. The general spatial patterns in nutrient concentrations did not reflect net mineralization/immobilization rates measured at our control or drained peatlands. Rather, the spatial patterns in nutrient availability may be regulated by differences in vegetation (mainly Sphagnum moss) cover between control and drained sites and possibly differences in hydrologic connection between microforms. Our results suggest that microform distribution and composition within a peatland may be important for determining how peatland nutrient dynamics will respond to water table drawdown in northern peatlands, as some evidence of microtopographic differences in nutrient dynamics was found.     

Effects of short-term drying and irrigation on CO2 and CH4 production and emission from mesocosms of a northern bog and an alpine fen

Atmospheric CO₂ and CH₄ exchange in peatlands is controlled by water table levels and soil moisture, but impacts of short periods of dryness and rainfall are poorly known. We conducted drying-rewetting experiments with mesocosms from an ombrotrophic northern bog and an alpine, minerotrophic fen. Efflux of CO₂ and CH₄ was measured using static chambers and turnover and diffusion rates were calculated from depth profiles of gas concentrations. Due to a much lower macroporosity in the fen compared to the bog peat, water table fluctuated more strongly when irrigation was stopped and resumed, about 11 cm in the fen and 5 cm in the bog peat. Small changes in air filled porosity caused CO₂ and CH₄ concentrations in the fen peat to be insensitive to changes in water table position. CO₂ emission was by a factor of 5 higher in the fen than in the bog mesocosms and changed little with water table position in both peats. This was probably caused by the importance of the uppermost, permanently unsaturated zone for auto- and heterotrophic CO₂ production, and a decoupling of air filled porosity from water table position. CH₄ emission was <0.4 mmol m^?2 day^?1 in the bog peat, and up to >12.6 mmol m^?2 day^?1 in the fen peat, where it was lowered by water table fluctuations. CH₄ production was limited to the saturated zone in the bog peat but proceeded in the capillary fringe of the fen peat. Water table drawdown partly led to inhibition of methanogenesis in the newly unsaturated zone, but CH₄ production appeared to continue after irrigation without time-lag. The identified effects of irrigation on soil moisture and respiration highlight the importance of peat physical properties for respiratory dynamics; but the atmospheric carbon exchange was fairly insensitive to the small-scale fluctuations induced.     

Sphagnum re-introduction in degraded peatlands: The effects of aggregation,species identity and water table

In European peatlands which have been drained and cut-over in the past, re-vegetation often stagnates after the return of a species-poor Sphagnum community. Re-introduction of currently absent species may be a useful tool to restore a typical, and more diverse, Sphagnum vegetation and may ultimately improve the functioning of peatland ecosystems, regarding atmospheric carbon sequestration. Yet, the factors controlling the success of re-introduction are unclear. In Ireland and Estonia, we transplanted small and large aggregates of three Sphagnum species into existing vegetation. We recorded changes in cover over a 3-year period, at two water levels (?5 and ?20 cm).Performance of transplanted aggregates of Sphagnum was highly species specific. Hummock species profited at low water tables, whereas hollow species profited at high water tables. But our results indicate that performance and establishment of species was also promoted by increased aggregate size. This mechanism (positive self-association) has earlier been seen in other ecosystems, but our results are the first to show this mechanism in peatlands. Our results do not agree with present management, which is aimed at retaining water on the surface of peat remnants in order to restore a functional and diverse Sphagnum community. More than the water table, aggregate size of the reintroduced species is crucial for species performance, and ultimately for successful peatland restoration.     

North American approach to the restoration of Sphagnum dominated peatlands

Sphagnum dominated peatlands do not rehabilitate well after being cutover (mined) for peat and some action needs to be taken in order to restore these sites within a human generation. Peatland restoration is recent and has seen significant advances in the 1990s. A new approach addressing the North American context has been developed and is presentedin this paper. The short-term goal of this approach is to establish a plant cover composed of peat bog species and to restore a water regime characteristic of peatland ecosystems. The long-term objective is to return the cutover areas to functional peat accumulating ecosystems. The approach developed for peatland restoration in North America involves the following steps: 1)field preparation, 2) diaspore collection, 3) diaspore introduction, 4) diaspore protection, and 5) fertilization. Field preparation aims at providing suitable hydrological conditions for diaspores through creation of microtopography and water retention basins, re-shaping cutover fields and blocking ditches. It is site specific because it depends largely onlocal conditions. The second step is the collection of the top 10 centimetres of the living vegetation in a natural bog as a source of diaspores. It is recommended to use a ratio of surface collected to surface restored between 1: 10 and 1: 15 in order to minimize the impact on natural bogs and to insure rapid plant establishment in less than four years. Diaspores are then spread as a thin layer on the bare peat surfaces to be restored. It has been demonstrated that too scant or too thick a layer decreases plant establishment success. Diaspores are then covered by a straw mulch applied at a rate of 3 000 kg ha^-1 which provides improved water availabilityand temperature conditions. Finally, phosphorus fertilization favours more rapid substrate colonization by vascular plants, which have been shown to help stabilize the bare peat surface and act as nurse plants to the Sphagnum mosses.     

Effect of peat re-wetting on carbon and nutrient fluxes, greenhouse gas production and diversity of methanogenic archaeal community

Many peatlands were affected by drainage in the past, and restoration of their water regime aims to bring back their original functions. The purpose of our study was to simulate re-wetting of soils of different types of drained peatlands (bogs and minerotrophic mires, located in the Sumava Mountains, Czech Republic) under laboratory conditions (incubation for 15 weeks) and to assess possible risks of peatland water regime restoration - especially nutrient leaching and the potentials for CO₂ and CH₄ production. After re-wetting of soils sampled from drained peatlands (simulated by anaerobic incubation) (i) phosphorus concentration (SRP) did not change in any soil, (ii) concentration of ammonium and dissolved organic nitrogen (DON) increased, but only in a drained fen, (iii) DOC increased significantly in the drained fen and degraded drained bog, (iv) CO₂ production decreased, (v) CH₄ production and the number of methanogens increased in all soils, and (vi) archaeal methanogenic community composition was also affected by re-wetting; it differed significantly between drained and pristine fens, whereas it was more similar between drained and pristine bogs. Overall, the soils from fens reacted more dynamically to re-wetting than the bogs, and therefore, some nutrients (especially nitrogen) and DOC leaching may be expected from drained fens after their water regime restoration. However, if compared to their state before restoration, ammonium and phosphorus leaching should not increase and leaching of nitrates and DON should even decrease after restoration, especially during the vegetation season. Further, CO₂ production in soils of fens and bogs should decrease after their water regime restoration, whereas CH₄ production in soils should increase. However, we cannot derive any clear conclusions about CH₄ emissions from the ecosystems based on this study, as they depend strongly on environmental factors and on the actual activity of methanotrophs in situ.     

Growing season carbon gas exchange from peatlands used as a source of vegetation donor material for restoration

The moss layer transfer technique removes the top layer of vegetation from donor sites as a method to transfer propagules and restore degraded or reclaimed peatlands. As this technique is new, little is known about the impacts of moss layer transfer on vegetation and carbon fluxes following harvest. We monitored growing season carbon dioxide (CO₂) and methane (CH₄) fluxes as well as plant communities at donor sites and neighbouring natural peatland sites in an ombrotrophic bog and minerotrophic fen in Alberta, Canada from which material was harvested between 1 and 6 years prior to the study. Plant recovery at all donor sites was rapid with an average of 72% total plant cover one growing season after harvest at the fen and an average of 87% total plant cover two growing seasons after harvest at the bog. Moss cover also returned, averaging 84% 6 years after harvest at the bog. The majority of natural peatlands in western Canada are treed and tree recruitment at the donor sites was limited. Methane emissions were higher from donor sites compared to natural sites due to the high water table and greater sedge cover. Carbon budgets suggested that the donor fen and bog sites released higher CO₂ and CH₄ over the growing season compared to adjacent natural sites. However, vegetation re-establishment on donor sites was rapid, and it is possible that these sites will return to their original carbon-cycle functioning after disturbance, suggesting that donor sites may recover naturally without implementing management strategies.     

Using palaeoecology to support blanket peatland management

Many peatlands have a recent history of being degraded by extraction, drainage, burning, overgrazing and atmospheric pollution often leading to erosion and loss of peat mass. Restoration schemes have been implemented aimed at rewetting peatlands, encouraging revegetation of bare peat or shifting the present vegetation assemblage to an alternative. Here we demonstrate the use of palaeoecological techniques that allow reconstruction of the historical development of a blanket peatland and provide a historical context from which legitimate restoration targets can be determined and supported. We demonstrate the applicability of simple stratigraphic techniques to provide a catchment-wide peatland development history and reinforce this with a detailed macrofossil reconstruction from a central core. Analysis at Keighley Moor Reservoir Catchment in northern England showed that the present vegetation state was ‘atypical’ and has been characteristic for only the last c. 100 years. Sphagnum moss was an important historic contributor to the vegetation cover between 1500 years ago and the early 1900s. Until the early 1900s Sphagnum occurrence fluctuated with evidence of fire, routinely returning after fire demonstrating good resilience of the ecosystem. However, from the turn of the 20th century, Sphagnum levels declined severely, coincident initially with a wildfire event but remaining extremely diminished as the site regularly underwent managed burning to support grouse moor gun sports where practitioners prefer a dominant cover of heather. It is suggested that any intention to alter land management at the site to raise water tables and encourage greater Sphagnum abundance is in line with peatland development at the site over the past 1500 years. Similar palaeoecological studies providing historical context could provide support for restoration targets and changes to peatland management practice for sites globally.     

Sedge Succession and Peatland Methane Dynamics: A Potential Feedback to Climate Change

Under the warmer climate, predicted for the future, northern peatlands are expected to become drier. This drying will lower the water table and likely result in reduced emissions of methane (CH₄) from these ecosystems. However, the prediction of declining CH₄ fluxes does not consider the potential effects of ecological succession, particularly the invasion of sedges into currently wet sites (open water pools, low lawns). The goal of this study was to characterize the relationship between the presence of sedges in peatlands and CH₄ efflux under natural conditions and under a climate change simulation (drained peatland). Methane fluxes, gross ecosystem production, and dissolved pore water CH₄ concentrations were measured and a vegetation survey was conducted in a natural and drained peatland near St. Charles-de-Bellechasse, Quebec, Canada, in the summer of 2003. Each peatland also had plots where the sedges had been removed by clipping. Sedges were larger, more dominant, and more productive at the drained peatland site. The natural peatland had higher CH₄ fluxes than the drained peatland, indicating that drainage was a significant control on CH₄ flux. Methane flux was higher from plots with sedges than from plots where sedges had been removed at the natural peatland site, whereas the opposite case was observed at the drained peatland site. These results suggest that CH₄ flux was enhanced by sedges at the natural peatland site and attenuated by sedges at the drained peatland site. However, the attenuation of CH₄ flux due to sedges at the drained site was reduced in wetter periods. This finding suggests that CH₄ flux could be decreased in the event of climate warming due to the greater depth to the water table, and that sedges colonizing these areas could further attenuate CH₄ fluxes during dry periods. However, during wet periods, the sedges may cause CH₄ fluxes to be higher than is currently predicted for climate change scenarios.     

The Effects of Peatland Restoration on Water‐Table Depth,Elemental Concentrations,and Vegetation: 10 Years of Changes

We studied the effects of restoration on water‐table depth (WTD), element concentrations of peat and vegetation composition of peatlands drained for forestry in southern Finland. The restoration aimed to return the trajectory of vegetation succession toward that of undisturbed systems through the blockage of ditches and the removal of trees. Permanent plots established on a bog and a fen were sampled 1 year before, and 1, 2, 3, and 10 years after the restoration. The restoration resulted in a long‐term rise of the water‐table in both peatlands. Ten years after restoration, the mineral element concentrations (Ca, K, Mg, Mn, and P) of peat corresponded to those reported from comparable pristine peatlands. In particular, the increase of K and Mn concentrations at both sites suggests the recovery of ecosystem functionality in terms of nutrient cycling between peat and plants. The restoration resulted in the succession of plant communities toward the targeted peatland vegetation of wetter condition at both sites. This was evident from the decreased abundance of species benefiting from drainage and the corresponding increase of peatland species. However, many species typical of pristine peatlands were missing 10 years after restoration. We conclude that the restoration led to a reversal of the effects of drainage in vegetation and studied habitat conditions. However, due to the slow recovery of peatland ecosystems and the possibility that certain failures in the restoration measures may become apparent only after extended time periods, long‐term monitoring is needed to determine whether the goals of restoration will be met.     

Organic matter accumulation in a restored peatland: Evaluating restoration success

Recent advances in peatland restoration techniques have succeeded in establishing Sphagnum moss on the remnant cutover peat surface following peat extraction; however, evaluating restoration success remains a key issue. We argue that a Sphagnum-dominated peatland can only be considered functionally ‘restored’ once organic matter accumulation has achieved a thickness where the mean water table position in a drought year does not extend into the underlying formerly cutover peat surface. Here we monitor the spatio-temporal development of organic matter accumulation in a new peat layer for the first 8 years following the restoration of a Québec peatland and couple a simple acrotelm carbon accumulation model and ecohydrological model to assess peatland restoration success.We determined that organic matter accumulation increased from 2.3 ± 1.7 cm 4 years post-restoration to 13.6 ± 6.5 cm 8 years post-restoration. For comparison, at an adjacent non-restored section of the peatland organic matter accumulation was significantly lower (p < 0.001 for all years), with mean thicknesses of 0.2 ± 0.6 and 0.8 ± 1.2 cm for 24 and 28 years post-extraction, respectively. Given the mean summer water deficit at the site (?64 mm), our ecohydrological modeling results suggest that a 19-cm-thick moss layer would be required to offset the water table decrease induced by the summer water deficit. Given the current rate of organic matter accumulation, net primary productivity and the new peat layer decomposition rates determined using litter bags, we estimate it will take 17 years post-restoration to accumulate a 19-cm moss layer. Consequently, we argue that successful peatland restoration may be achieved in the medium-term and that our simple modeling approach can be useful in assessing the long-term impact of restoration on atmospheric carbon dioxide sequestration.     

Do birds of a feather flock together? Comparing habitat preferences of piscivorous waterbirds in a lowland river catchment

The aim of the present study was to use the analysis of surface water chemistry to understand vegetation succession pathways in terrestrializing polyhumic lakes. We hypothesized that Sphagnum mire development was accompanied by a decrease in the mineral content in water. A total of 111 vegetation plots along 23 transects were analysed in 11 lakes and adjacent peat lands in the Wigry National Park (NE Poland). The vegetation of the lake-mire systems forms distinct zones: (1) nymphaeid-, bladderwort- and bryophyte-dominated aquatic vegetation; (2) sedge-dominated edge of the Sphagnumcarpet; (3) quaking, extremely poor fen with various Cyperaceae; (4) non-quaking, Eriophorum vaginatum-dominated bog-like vegetation and (5) pine woodland. Surface water corrected conductivity (EC_corr.), pH, COD-KMnO₄ and Ca²⁺, Mg²⁺, Fetot. and SiO₂ were measured along the transects. The environmental gradients best explaining the observed pattern were pH (with the highest values in the lake and the lowest in the bog-like vegetation) and COD-KMnO₄ (showing an inverse direction). At least in some Sphagnum-mires conditions were more minerotrophic than in the lakes. The process of humic lake overgrowing by Sphagnum-mires in NE Poland results in pine woodlands on mineralised peat. The climate conditions in NE Poland, combined with evapotranspiration accelerated by encroaching trees, do not seem to support the development of ombrotrophic bogs.     

Boreal peatland ecosystems under enhanced UV-B radiation and elevated tropospheric ozone concentration

Boreal peat-forming wetlands, mires, are globally important sources of methane and sinks for CO₂. As peatland vegetation plays a significant role regulating the exchange of these greenhouse gases, we have assessed the responses of the dominant plants and ecosystem functions to increasing tropospheric ozone concentration and enhanced ultraviolet-B (UV-B) radiation in long-term experiments, the results of which are summarized in this review. The dominant sedge, Eriophorum vaginatum, and especially the Sphagnum mosses common on peatlands, appear fairly tolerant to the future predicted ozone levels. Similarly, UV-B radiation only caused few alterations in the carbohydrates and pigments of the dominant sedge, Eriophorum russeolum, and had no effects on the dominant moss species of the experimental site, Warnstorfia exannulata. Surprisingly, there were alterations in organic acid concentrations in the peat pore water and peat microbial community composition in both experiments. Elevated ozone caused a transient decrease in ecosystem-level gross photosynthesis and methane (CH₄) emission, which shifted to a slight increase later on. Enhanced UV-B decreased dark ecosystem respiration and increased CH₄ emission in the course of the six measurement years. The emission of isoprene was increased by both ozone and UV-B during warm weather periods, suggesting interactive effects with temperature. All in all, we suggest that ozone and UV-B have limited effects on the carbon cycle in boreal peatlands, because other environmental factors, such as temperature, water level and photosynthetically active radiation more strongly regulate CO₂ and CH₄ exchange rates.     

Peat CO2 production in a natural and cutover peatland: Implications for restoration

Although studies have shown that peatland drainage andharvesting alter local hydrology, microclimate, and peatcharacteristics, little is known about the effects of these changes onCO₂ production rates. This study examines the differentfactors affecting CO₂ production from natural and cutoverpeatlands. Laboratory peat incubations were performed under aerobic andanaerobic conditions to determine the influence of temperature, soilmoisture, and peat depth on CO₂ production rates from peatsamples taken from: (1) a natural peatland; (2) a 2-yearpost-cutover peatland and; (3) a 7-year post-cutover peatland.CO₂ production rates ranged from 0.21 to 4.87 µmolg^–1 d^–1 under anaerobic conditions,and from 0.37 to 15.69 µmol g^–1d^–1 in the aerobic trials. While no significantdifferences were found between the CO₂ production rates ofthe two cutover sites, the natural site consistently displayed higherproduction values. The natural site was also the only site to exhibitstrong depth dependent trends, thus indicating the importance of theupper peat layer with respect to substrate quality. Higher productionrates were found under aerobic than anaerobic conditions, with thegreatest response to oxygen observed at the natural site. Productionrates increased with both temperature and soil moisture, with maximumproduction rates found at 20 °C and 92% moisture content.Temperature responses were generally greater at the cutover sites, whilesoil moisture had greater effects on the natural site peat.Results of this work agree with previous studies that suggest that itis essential to begin restoration once a cutover peatland is abandoned.Re-wetting a cutover peatland (through restoration practices) isnecessary to prevent an increase in peat temperature and CO₂production since cutover peat has higher Q₁₀ values thannatural peat. A decrease in overall peatland oxidation should reduce thepersistent source of atmospheric CO₂ from cutover peatlandsand the irreversible changes in peat structure that impedeSphagnum re-establishment.     

Comparison of carbon and nitrogen accumulation rate between bog and fen phases in a pristine peatland with the fen-bog transition

Long-term carbon and nitrogen dynamics in peatlands are affected by both vegetation production and decomposition processes. Here, we examined the carbon accumulation rate (CAR), nitrogen accumulation rate (NAR) and δ¹³C, δ¹⁵N of plant residuals in a peat core dated back to ~8500 cal year BP in a temperate peatland in Northeast China. Impacted by the tephra during 1160 and 789 cal year BP and climate change, the peatland changed from a fen dominated by vascular plants to a bog dominated by Sphagnum mosses. We used the Clymo model to quantify peat addition rate and decay constant for acrotelm and catotelm layers during both bog and fen phases. Our studied peatland was dominated by Sphagnum fuscum during the bog phase (789 to −59 cal year BP) and lower accumulation rates in the acrotelm layer was found during this phase, suggesting the dominant role of volcanic eruption in the CAR of the peat core. Both mean CAR and NAR were higher during the bog phase than during the fen phase in our study, consistent with the results of the only one similar study in the literature. Because the input rate of organic matter was considered to be lower during the bog phase, the decomposition process must have been much lower during the bog phase than during the fen phase and potentially controlled CAR and NAR. During the fen phase, CAR was also lower under higher temperature and summer insolation, conditions beneficial for decomposition. δ¹⁵N of Sphagnum hinted that nitrogen fixation had a positive effect on nitrogen accumulation, particular in recent decades. Our study suggested that decomposition is more important for carbon and nitrogen sequestration than production in peatlands in most conditions and if future climate changes or human disturbance increase decomposition rate, carbon sequestration in peatlands will be jeopardized.     

Mechanisms involved in the re-establishment of Sphagnum-dominated vegetation in rewetted bog remnants

Restoration of peat bog vegetation inhighly degraded peatlands is generallyattempted by improving the hydrology ofthese areas. The present paper discussesand explains various restoration strategiesrelating to peat quality, water chemistryand hydrology. In some cases, (shallow)inundation of bog remnants leads to a rapidredevelopment of (floating) Sphagnumvegetation, usually when poorly humifiedSphagnum peat is still present. Afterinundation, the peat either swells up tothe newly created water table or becomesbuoyant, in both cases creating a favorablesubstrate for Sphagnum mosses. Bulkdensity and methane production rate play animportant role in the buoyancy of floatingpeat, methane providing buoyancy to thesubstrates. The presence of (slightly)calcareous groundwater in the peat base mayenhance the development of floating raftsby stimulating decomposition processes.Alternatively, the growth of submerged Sphagnum species can also lead to thedevelopment of floating rafts. This dependson the penetration of light into the waterlayer and the availability of carbondioxide in the water layer.Many bog remnants, however, only havestrongly humified peat, which does notfavor the redevelopment of Sphagnumcarpets after deep inundation. On the otherhand, most peat moss species appear to dovery well on surface soaked black peat,which is why shallow inundation (< 0.3 m)is to be preferred in such cases.Compartmentalization of the terrain willprobably be necessary to ensure a more orless constant water table.An important prerequisite for thesuccessful restoration of bog remnants isthe development of a hydrologicallyself-regulating acrotelm. Key speciesinvolved in this development are Sphagnum magellanicum, Sphagnumpapillosum and Sphagnum rubellum.These typical hummock and lawn species areusually very slow colonizers compared tohollow species such as Sphagnumcuspidatum and Sphagnum fallax.Introduction of key species in carpetsdominated by hollow species or on baresubstrates appears to be very successful,indicating that the main constraint iscolonization.     

Warming impacts on boreal fen CO2 exchange under wet and dry conditions

Northern peatlands form a major soil carbon (C) stock. With climate change, peatland C mineralization is expected to increase, which in turn would accelerate climate change. A particularity of peatlands is the importance of soil aeration, which regulates peatland functioning and likely modulates the responses to warming climate. Our aim is to assess the impacts of warming on a southern boreal and a sub‐arctic sedge fen carbon dioxide (CO₂) exchange under two plausible water table regimes: wet and moderately dry. We focused this study on minerotrophic treeless sedge fens, as they are common peatland types at boreal and (sub)arctic areas, which are expected to face the highest rates of climate warming. In addition, fens are expected to respond to environmental changes faster than the nutrient poor bogs. Our study confirmed that CO₂ exchange is more strongly affected by drying than warming. Experimental water level draw‐down (WLD) significantly increased gross photosynthesis and ecosystem respiration. Warming alone had insignificant impacts on the CO₂ exchange components, but when combined with WLD it further increased ecosystem respiration. In the southern fen, CO₂ uptake decreased due to WLD, which was amplified by warming, while at northern fen it remained stable. As a conclusion, our results suggest that a very small difference in the WLD may be decisive, whether the C sink of a fen decreases, or whether the system is able to adapt within its regime and maintain its functions. Moreover, the water table has a role in determining how much the increased temperature impacts the CO₂ exchange.