Delineating boreal plains bog margin ecotones across hydrogeological settings for wildfire risk management

Canada’s Boreal Plains peatland vegetation species assemblages are characterized by their functional ecosystem roles and feedbacks, which are important for carbon and water storage in a sub-humid climate. The vegetation communities at the peatland-upland interface, or the peatland margin ecotone, have not been extensively delineated or characterized as a distinct ecotone. Because these ecotones constitute a smouldering “hotspot” during wildfire, with carbon loss from these margins accounting for 50–90% of total peatland carbon loss, their delineation is critical. Post-fire, areas of severe peat smouldering have previously been shown to undergo shifts in vegetation community composition, resulting in a loss of key peatland ecohydrological functions. The aim of this study was to delineate Boreal Plains peatland margin ecotones and assess their prevalence across the landscape. Using split moving window analysis on vegetation transect data from a chronosequence of study sites, the margin ecotones were delineated at sites having different times since fire. No significant differences were identified in margin width over time or margin peat depths across hydrogeological settings. However, with peat depths of up to 2.46 m in small peatlands characteristic of moraine and glaciofluvial deposits, vulnerable margin peat has been demonstrated to represent a significant carbon store. Fire managers employing peatland fuel treatments for wildfire abatement and community protection should consider these confined peatlands more carefully to mitigate catastrophic carbon losses. Further, we suggest that a greater understanding is needed of the roles of peatland margin ecotones in sustaining peatland autogenic feedback mechanisms that promote paludification and recovery following wildfire.     

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.     

Positive trends in plant,dragonfly, and butterfly diversity of rewetted montane peatlands

Drainage and afforestation of peatlands cause extensive habitat degradation and species losses. Restoration supports peatland biodiversity by creating suitable habitat conditions, including stable high water tables. However, colonization by characteristic species can take decades or even fail. Peatland recovery is often monitored shortly after restoration, but initial trends may not continue, and results might differ among taxonomic groups. This study analyzes trends in plant, dragonfly, and butterfly diversity within 18 years after rewetting of montane peatlands in central Germany. We compared diversity and species composition of 19 restored sites with three drained peatlands and one near‐natural reference site. Restoration resulted in improved habitat conditions and benefited species diversity, but there were marked differences among taxonomic groups. Dragonflies rapidly colonized small water bodies but their diversity did not further increase in older restoration sites. Characteristic peatland vegetation recovered slowly, since it depended on a high water holding capacity that was only reached after peat started accumulating. Generally, plant diversity developed toward reference conditions albeit incompletely, even 18 years after restoration. Butterflies responded less to peatland restoration; generalists increased only temporarily and specialists could not establish. In conclusion, peatland restoration improves habitat conditions and biodiversity, while trajectories of recovery are nonlinear and incomplete after two decades. This highlights the need for long‐term monitoring and a strategic selection of indicator species for evaluation of restoration success.     

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.     

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.     

Animal and vegetation patterns in natural and man-made bog pools: implications for restoration

1. Peatlands have suffered great losses following drainage for agriculture, forestry, urbanisation, or peat mining, near inhabited areas. We evaluated the faunal and vegetation patterns after restoration of a peatland formerly mined for peat. We assessed whether bog pools created during restoration are similar to natural bog pools in terms of water chemistry, vegetation structure and composition, as well as amphibian and arthropod occurrence patterns. 2. Both avian species richness and peatland vegetation cover at the site increased following restoration. Within bog pools, however, the vegetation composition differed between natural and man‐made pools. The cover of low shrubs, Sphagnum moss, submerged, emergent and floating vegetation in man‐made pools was lower than in natural pools, whereas pH was higher than in typical bog pools. Dominant plant species also differed between man‐made and natural pools. 3. Amphibian tadpoles, juveniles and adults occurred more often in man‐made pools than natural bog pools. Although some arthropods, including Coleoptera bog specialists, readily colonised the pools, their abundance was two to 26 times lower than in natural bog pools. Plant introduction in bog pools, at the stocking densities we applied, had no effect on the occurrence of most groups. 4. We conclude that our restoration efforts were partially successful. Peatland‐wide vegetation patterns following restoration mimicked those of natural peatlands, but 4 years were not sufficient for man‐made pools to fully emulate the characteristics of natural bog pools.     

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.     

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.     

Evidence for older carbon loss with lowered water tables and changing plant functional groups in peatlands

A small imbalance in plant productivity and decomposition accounts for the carbon (C) accumulation capacity of peatlands. As climate changes, the continuity of peatland net C storage relies on rising primary production to offset increasing ecosystem respiration (ER) along with the persistence of older C in waterlogged peat. A lowering in the water table position in peatlands often increases decomposition rates, but concurrent plant community shifts can interactively alter ER and plant productivity responses. The combined effects of water table variation and plant communities on older peat C loss are unknown. We used a full-factorial 1-m³ mesocosm array with vascular plant functional group manipulations (Unmanipulated Control, Sedge only, and Ericaceous only) and water table depth (natural and lowered) treatments to test the effects of plants and water depth on CO₂ fluxes, decomposition, and older C loss. We used Δ¹⁴C and δ¹³C of ecosystem CO₂ respiration, bulk peat, plants, and porewater dissolved inorganic C to construct mixing models partitioning ER among potential sources. We found that the lowered water table treatments were respiring C fixed before the bomb spike (1955) from deep waterlogged peat. Lowered water table Sedge treatments had the oldest dissolved inorganic ¹⁴C signature and the highest proportional peat contribution to ER. Decomposition assays corroborated sustained high rates of decomposition with lowered water tables down to 40 cm below the peat surface. Heterotrophic respiration exceeded plant respiration at the height of the growing season in lowered water table treatments. Rates of gross primary production were only impacted by vegetation, whereas ER was affected by vegetation and water table depth treatments. The decoupling of respiration and primary production with lowered water tables combined with older C losses suggests that climate and land-use-induced changes in peatland hydrology can increase the vulnerability of peatland C stores.     

Macrophyte loss drives decadal change in benthic invertebrates in peatland drainage ditches

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Vegetation composition dynamics in peatlands used as buffer areas in forested catchments in southern and central Finland

Peatland buffer areas are important means in reducing sediment and nutrient loading from discharge waters in a variety of landscapes; however, use of natural mires as buffer areas may induce unwanted changes in the plant species composition. Vegetation composition dynamics were studied at one rewetted peatland and two natural peatlands used as buffer areas in forested catchments in southern and central Finland. In addition to the sediment and nutrient loads from the upstream catchments, the buffer areas received nitrogen and phosphorus from two artificial additions made in 2003?C2005 and 2008 in order to simulate loads caused by forestry operations. The first vegetation inventory was done in the year of buffer construction (1996 or 2000), the second inventory 4?C5?years after the first one, and the third inventory after 9?C13?years. The vegetation composition changed significantly at all three buffer areas. Grasses and sedges, as well as herbs were generally favored by the use of peatlands as buffer areas, and at the species level, the coverages of Menyanthes trifoliata and Calamagrostis purpurea increased the most. At the two natural sites, the change in vegetation composition was more apparent in the upstream parts of the buffer areas, probably because they received more sediments and nutrients than the lower parts. Also, the vegetation changed significantly more in the lawn-level surfaces than in the hummocks. As the vegetation composition in natural peatlands used as buffer areas is likely to undergo significant changes, the use of endangered mire site types should be avoided.     

The influence of local elevation on soil properties and tree health in remnant eucalypt woodlands affected by secondary salinity

More than 2 M ha of remnant vegetation in Australia is predicted to be at risk from shallow water tables by 2050. Currently, vegetation is considered to be at risk where the water table is predicted to be less than 2 m below the soil surface, yet casual observation of areas affected by secondary salinity in the Western Australian wheatbelt has suggested that small differences in elevation (< 0.5 m) are important in determining plant health. In this study, we investigated how small changes in elevation (and hence depth to the water table) affected soil Cl concentrations and water contents, and whether small changes in elevation were associated with major changes in tree health in two remnants of Eucalyptus wandoo Blakely woodland with secondary salinity. At one site there were strong dissimilarities between soil samples collected above or below relative elevations of 0.5 m in areas with a shallow (0.3 m deep in September 2001) and saline water table. This was reflected in almost complete tree mortality at relative elevations below 0.5 m. However, low rainfall in 2001 meant that it was unlikely that current soil conditions had caused tree death. When water table data for 1999 was overlaid over plots of tree health and transect topography, high levels of tree mortality corresponded with areas where the water table was at or above the ground surface. At the other site, there was no clear relationship between elevation, soil characteristics and tree health. Localised variation in abiotic conditions and ecosystem processes at a fine-scale may buffer, to some extent, the spatial impact of soil salinity and waterlogging in remnant vegetation. Collapses in tree health at some sites are likely to be related to extreme and episodic events, which we may have limited ability to predict.     

Chemical and botanical indicators of groundwater inflow to Sphagnum-dominated peatlands

Knowledge of whether a peatland is fed by a surface aquifer or is providing water to the aquifer can lead to different aquifer and wetland management strategies. Few studies have been conducted to investigate aquifer-peatland connections, because flow connections are difficult to measure and can be spatially and temporally variable. The objective of this study was to combine chemical and botanical indicators of groundwater inflow to Sphagnum-dominated peatlands for a better classification of their water sources. Available knowledge of peatland geomorphic setting, water chemistry, and vegetation data for 12 aquifer-peatland systems of the Abitibi-Temiscamingue region and of the St. Lawrence Lowlands, two contrasting regions of southern Quebec (Canada), were used to derive indicators of groundwater inflow. Total dissolved solids (TDS) is identified as a comprehensive indicator of water mineralization. Threshold values of 16 mg/l (Abitibi-Temiscamingue) and 22 mg/l (St. Lawrence Lowlands) were found to indicate the presence of groundwater within the peatland. Results show that combining chemical (TDS) and botanical indicators can detect the presence of groundwater inflow into most of the studied peatlands. The indicators are more efficient on slope peatlands, where groundwater inflow is more substantial and less spatially variable, than in basin peatlands. A two-step approach is proposed: (1) identify the geomorphic setting of the peatland, and (2) estimate the chemical and botanical indicators. This approach is low-cost and easy to implement, and thus can be used on a large number of sites to assess the presence of groundwater inflow to peatlands.     

Patterns of Fungal and Bacterial Carbon Mineralization Across Northern European Peatlands

The fungal and bacterial activity was determined in 20 northern European peatlands ranging from ombrotrophic bogs to eutrophic fens with key differences in degree of humification, pH, dry bulk density, carbon (C) content and vegetation communities using the selective inhibition (SI) technique. These peatlands were partly disturbed and the respective water tables lowered below the surface layer. Basal respiration ranged from 24 to 128 µg CO₂-C g^?1 dry peat d^?1. Bacterial contributions to CO₂ production were high in most peatlands and showed the following pattern: eutrophic >> transitional ≥ mesotrophic >> ombrotrophic peatland types. The fungal-to-bacterial (F:B) ratios varied substantially within peatland type, and this was mainly attributed to differences in peat botanical compositions and chemistry. The computed mean Inhibitor Additivity Ratio (IAR) was quite close to 1 to suggest that the SI techniques can be used to partition eukaryotic and prokaryotic activity in wide range of peatlands. Overall, basal respiration, microbial biomass-C, fungal and bacterial activities varied across the studied peatland types, and such differences could have consequences for C- and nutrient-cycling as well as how bogs and fens will respond to environmental changes.     

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.     

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.     

Consistent centennial-scale change in European sub-Arctic peatland vegetation toward Sphagnum dominance—Implications for carbon sink capacity

Climate warming is leading to permafrost thaw in northern peatlands, and current predictions suggest that thawing will drive greater surface wetness and an increase in methane emissions. Hydrology largely drives peatland vegetation composition, which is a key element in peatland functioning and thus in carbon dynamics. These processes are expected to change. Peatland carbon accumulation is determined by the balance between plant production and peat decomposition. But both processes are expected to accelerate in northern peatlands due to warming, leading to uncertainty in future peatland carbon budgets. Here, we compile a dataset of vegetation changes and apparent carbon accumulation data reconstructed from 33 peat cores collected from 16 sub-arctic peatlands in Fennoscandia and European Russia. The data cover the past two millennia that has undergone prominent changes in climate and a notable increase in annual temperatures toward present times. We show a pattern where European sub-Arctic peatland microhabitats have undergone a habitat change where currently drier habitats dominated by Sphagnum mosses replaced wetter sedge-dominated vegetation and these new habitats have remained relatively stable over the recent decades. Our results suggest an alternative future pathway where sub-arctic peatlands may at least partly sustain dry vegetation and enhance the carbon sink capacity of northern peatlands.     

Multidate,multisensor remote sensing reveals high density of carbon‐rich mountain peatlands in the páramo of Ecuador

Tropical peatlands store a significant portion of the global soil carbon (C) pool. However, tropical mountain peatlands contain extensive peat soils that have yet to be mapped or included in global C estimates. This lack of data hinders our ability to inform policy and apply sustainable management practices to these peatlands that are experiencing unprecedented high rates of land use and land cover change. Rapid large‐scale mapping activities are urgently needed to quantify tropical wetland extent and rate of degradation. We tested a combination of multidate, multisensor radar and optical imagery (Landsat TM/PALSAR/RADARSAT‐1/TPI image stack) for detecting peatlands in a 2715 km² area in the high elevation mountains of the Ecuadorian páramo. The map was combined with an extensive soil coring data set to produce the first estimate of regional peatland soil C storage in the páramo. Our map displayed a high coverage of peatlands (614 km²) containing an estimated 128.2 ± 9.1 Tg of peatland belowground soil C within the mapping area. Scaling‐up to the country level, páramo peatlands likely represent less than 1% of the total land area of Ecuador but could contain as much as ~23% of the above‐ and belowground vegetation C stocks in Ecuadorian forests. These mapping approaches provide an essential methodological improvement applicable to mountain peatlands across the globe, facilitating mapping efforts in support of effective policy and sustainable management, including national and global C accounting and C management efforts.     

Status and restoration of peatlands in northern Europe

Environmental management of peatlands,landscape ecology and protection of keybiotopes have created needs and pressure torestore drained peatlands to natural mireecosystems. Here, we summarize differentapproaches and restoration techniquesdeveloped for peatland management inEstonia, Sweden, and Finland wherepeatlands are abundant. Without rewetting,plant colonisation on abandoned cut-awayareas is slow due to harsh hydrological andmicroclimatic conditions. However, after restoration, cut-away peatlands may returnto a functional state close to that ofpristine mires, and therefore restore a netcarbon sink function within a few years. Inaddition, restoration techniques can helpto create buffer zones between terrestrialand limnic ecosystems that reduces thenutrient loading imposed on watercourses byforestry operations. Restoration may alsobe important for peatland conservationprograms as drained peatlands are part ofpresent and future conservation areas.Finally, restoration actions in themselvescan have negative environmental impacts.For instance, inundation of peat surfacesresulting from the rewetting process oftenincreases phosphorus leaching. Efforts onpeatland restoration should focus onenvironmental monitoring, research onrestoration and its environmental impact aswell as public relations activities. Inthat respect, knowledge transfer betweenacademics and managers should generatesynergy benefits.     

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.