Peatlands and the carbon cycle: from local processes to global implications - a synthesis

Peatlands cover only 3% of the Earth's land surface but boreal and subarctic peatlands store about 15-30% of the world's soil carbon ( C) as peat. Despite their potential for large positive feedbacks to the climate system through sequestration and emission of greenhouse gases, peatlands are not explicitly included in global climate models and therefore in predictions of future climate change. In April 2007 a symposium was held in Wageningen, the Netherlands, to advance our understanding of peatland C cycling. This paper synthesizes the main findings of the symposium, focusing on (i) small-scale processes, (ii) C fluxes at the landscape scale, and (iii) peatlands in the context of climate change. The main drivers controlling most are related to some aspects of hydrology. Despite high spatial and annual variability in Net Ecosystem Exchange ( NEE), the differences in cumulative annual NEE are more a function of broad scale geographic location and physical setting than internal factors, suggesting the existence of strong feedbacks. In contrast, trace gas emissions seem mainly controlled by local factors. Key uncertainties remain concerning the existence of perturbation thresholds, the relative strengths of the CO2 and CH4 feedback, the links among peatland surface climate, hydrology, ecosystem structure and function, and trace gas biogeochemistry as well as the similarity of process rates across peatland types and climatic zones. Progress on these research areas can only be realized by stronger co-operation between disciplines that address different spatial and temporal scales

Peat decomposition records in three pristine ombrotrophic bogs in southern Patagonia

Ombrotrophic bogs in southern Patagonia have been examined with regard to paleoclimatic and geochemical research questions but knowledge about organic matter decomposition in these bogs is limited. Therefore, we examined peat humification with depth by Fourier Transformed Infrared (FTIR) measurements of solid peat, C/N ratio, and δ<sup>13</sup>C and δ<sup>15</sup>N isotope measurements in three bog sites. Peat decomposition generally increased with depth but distinct small scale variation occurred, reflecting fluctuations in factors controlling decomposition. C/N ratios varied mostly between 40 and 120 and were significantly correlated (<i>R</i><sup>2</sup> > 0.55, <i>p</i> < 0.01) with FTIR-derived humification indices. The degree of decomposition was lowest at a site presently dominated by <i>Sphagnum</i> mosses. The peat was most strongly decomposed at the driest site, where currently peat-forming vegetation produced less refractory organic material, possibly due to fertilizing effects of high sea spray deposition. Decomposition of peat was also advanced near ash layers, suggesting a stimulation of decomposition by ash deposition. Values of δ<sup>13</sup>C were 26.5 ± 2‰ in the peat and partly related to decomposition indices, while δ<sup>15</sup>N in the peat varied around zero and did not consistently relate to any decomposition index. Concentrations of DOM partly related to C/N ratios, partly to FTIR derived indices. They were not conclusively linked to the decomposition degree of the peat. DOM was enriched in <sup>13</sup>C and in <sup>15</sup>N relative to the solid phase probably due to multiple microbial modifications and recycling of N in these N-poor environments. In summary, the depth profiles of C/N ratios, δ<sup>13</sup>C values, and FTIR spectra seemed to reflect changes in environmental conditions affecting decomposition, such as bog wetness, but were dominated by site specific factors, and are further influenced by ash deposition and possibly by sea spray input

Zero to moderate methane emissions in a densely rooted, pristine Patagonian bog – biogeochemical controls as revealed from isotopic evidence

Peatlands are significant global methane (CH4) sources, but processes governing CH4 dynamics have been predominantly studied in the Northern Hemisphere. Southern hemispheric and tropical bogs can be dominated by cushion-forming vascular plants (e.g. Astelia pumila, Donatia fascicularis). These cushion bogs are found in many (mostly southern) parts of the world but could also serve as extreme examples for densely rooted northern hemispheric bogs dominated by rushes and sedges. We report highly variable summer CH4 emissions from different microforms in a Patagonian cushion bog as determined by chamber measurements. Driving biogeochemical processes were identified from pore water profiles and carbon isotopic signatures. Intensive root activity throughout a rhizosphere stretching over 2&thinsp;m in depth accompanied by molecular oxygen release created aerobic microsites in water-saturated peat, leading to a thorough CH4 oxidation (&lt;&thinsp;0.003&thinsp;mmol&thinsp;L−1 pore water CH4, enriched in δ13C-CH4 by up to 10&thinsp;‰) and negligible emissions (0.09±0.16&thinsp;mmol&thinsp;CH4&thinsp;m−2&thinsp;d−1) from Astelia lawns. In sparsely or even non-rooted peat below adjacent pools pore water profile patterns similar to those obtained under Astelia lawns, which emitted very small amounts of CH4 (0.23±0.25&thinsp;mmol&thinsp;m−2&thinsp;d−1), were found. Below the A. pumila rhizosphere pore water concentrations increased sharply to 0.40±0.25&thinsp;mmol&thinsp;CH4&thinsp;L−1 and CH4 was predominantly produced by hydrogenotrophic methanogenesis. A few Sphagnum lawns and – surprisingly – one lawn dominated by cushion-forming D. fascicularis were found to be local CH4 emission hotspots with up to 1.52±1.10&thinsp;mmol&thinsp;CH4&thinsp;m−2&thinsp;d−1 presumably as root density and molecular oxygen release dropped below a certain threshold. The spatial distribution of root characteristics supposedly causing such a pronounced CH4 emission pattern was evaluated on a conceptual level aiming to exemplify scenarios in densely rooted bogs. We conclude that presence of cushion vegetation as a proxy for negligible CH4 emissions from cushion bogs needs to be interpreted with caution. Nevertheless, overall ecosystem CH4 emissions at our study site were probably minute compared to bog ecosystems worldwide and widely decoupled from environmental controls due to intensive root activity of A. pumila, for example.</p

Differential response of carbon cycling to long-term nutrient input and altered hydrological conditions in a continental Canadian peatland

Peatlands play an important role in global carbon cycling, but their responses to long-term anthropogenically changed hydrologic conditions and nutrient infiltration are not well known. While experimental manipulation studies, e.g., fertilization or water table manipulations, exist on the plot scale, only few studies have addressed such factors under in situ conditions. Therefore, an ecological gradient from the center to the periphery of a continental Canadian peatland bordering a eutrophic water reservoir, as reflected by increasing nutrient input, enhanced water level fluctuations, and increasing coverage of vascular plants, was used for a case study of carbon cycling along a sequence of four differently altered sites. We monitored carbon dioxide (CO2) and methane (CH4) surface fluxes and dissolved inorganic carbon (DIC) and CH4 concentrations in peat profiles from April 2014 through September 2015. Moreover, we studied bulk peat and pore-water quality and we applied δ13C–CH4 and δ13C–CO2 stable isotope abundance analyses to examine dominant CH4 production and emission pathways during the growing season of 2015. We observed differential responses of carbon cycling at the four sites, presumably driven by abundances of plant functional types and vicinity to the reservoir. A shrub-dominated site in close vicinity to the reservoir was a comparably weak sink for CO2 (in 1.5 years: -1093±794, in 1 year: +135±281 gCO2m-2; a net release) as compared to two graminoid-moss-dominated sites and a moss-dominated site (in 1.5 years: -1552 to -2260 gCO2m-2, in 1 year: -896 to -1282 gCO2m-2). Also, the shrub-dominated site featured notably low DIC pore-water concentrations and comparably 13C-enriched CH4 (δ13C–CH4: -57.81±7.03 ‰) and depleted CO2 (δ13C–CO2: -15.85±3.61 ‰) in a more decomposed peat, suggesting a higher share of CH4 oxidation and differences in predominant methanogenic pathways. In comparison to all other sites, the graminoid-mossdominated site in closer vicinity to the reservoir featured a ~30% higher CH4 emission (in 1.5 years: +61.4±32, in 1 year: +39.86±16.81 gCH4m-2). Low δ13C–CH4 signatures (-62.30±5.54 ‰) indicated only low mitigation of CH4 emissions by methanotrophic activity here. Pathways of methanogenesis and methanotrophy appeared to be related to the vicinity to the water reservoir: the importance of acetoclastic CH4 production apparently increased toward the reservoir, whereas the importance of CH4 oxidation increased toward the peatland center. Plant-mediated transport was the prevailing CH4 emission pathway at all sites even where graminoids were rare. Our study thus illustrates accelerated carbon cycling in a strongly altered peatland with consequences for CO2 and CH4 budgets. However, our results suggest that long-term excess nutrient input does not necessarily lead to a loss of the peatland carbon sink function

Peatland Initiation, Carbon Accumulation, and 2 ka Depth in the James Bay Lowland and Adjacent Regions

Copyright © 2014 University of Colorado at Boulder, Institute of Arctic and Alpine ResearchPeatlands surrounding Hudson and James Bays form the second largest peatland complex in the world and contain major stores of soil carbon (C). This study utilized a transect of eight ombrotrophic peat cores from remote regions of central and northern Ontario to quantify the magnitude and rate of C accumulation since peatland initiation and for the past 2000 calendar years before present (2 ka). These new data were supplemented by 17 millennially resolved chronologies from a literature review covering the Boreal Shield, Hudson Plains, and Taiga Shield bordering Hudson and James Bays. Peatlands initiated in central and northern Ontario by 7.8 ka following deglaciation and isostatic emergence of northern areas to above sea level. Total C accumulated since inception averaged 109.7 ± (std. dev.) 36.2 kg C m–2. Approximately 40% of total soil C has accumulated since 2 ka at an average apparent rate of 20.2 ± 6.9 g C m–2 yr–1. The 2 ka depths correlate significantly and positively with modern gridded climate estimates for mean annual precipitation, mean annual air temperature, growing degree-days > 0 °C, and photosynthetically active radiation integrated over days > 0 °C. There are significantly shallower depths in permafrost peatlands. Vertical peat accumulation was likely constrained by temperature, growing season length, and photosynthetically active radiation over the last 2 ka in the Hudson Bay Lowlands and surrounding regions.US National Science Foundatio

Anaerobic oxidation of methane associated with sulfate reduction in a natural freshwater gas source

The occurrence of anaerobic oxidation of methane (AOM) and trace methane oxidation (TMO) was investigated in a freshwater natural gas source. Sediment samples were taken and analyzed for potential electron acceptors coupled to AOM. Long-term incubations with 13C-labeled CH4 (13CH4) and different electron acceptors showed that both AOM and TMO occurred. In most conditions, 13C-labeled CO2 (13CO2) simultaneously increased with methane formation, which is typical for TMO. In the presence of nitrate, neither methane formation nor methane oxidation occurred. Net AOM was measured only with sulfate as electron acceptor. Here, sulfide production occurred simultaneously with 13CO2 production and no methanogenesis occurred, excluding TMO as a possible source for 13CO2 production from 13CH4. Archaeal 16S rRNA gene analysis showed the highest presence of ANME-2a/b (ANaerobic MEthane oxidizing archaea) and AAA (AOM Associated Archaea) sequences in the incubations with methane and sulfate as compared with only methane addition. Higher abundance of ANME-2a/b in incubations with methane and sulfate as compared with only sulfate addition was shown by qPCR analysis. Bacterial 16S rRNA gene analysis showed the presence of sulfate-reducing bacteria belonging to SEEP-SRB1. This is the first report that explicitly shows that AOM is associated with sulfate reduction in an enrichment culture of ANME-2a/b and AAA methanotrophs and SEEP-SRB1 sulfate reducers from a low-saline environment.We thank Douwe Bartstra (Vereniging tot Behoud van de Gasbronnen in Noord-Holland, The Netherlands), Carla Frijters (Paques BV, The Netherlands) and Teun Veuskens (Laboratory of Microbiology, WUR, The Netherlands) for sampling; Martin Meirink (Hoogheemraadschap Hollands Noorderkwartier, The Netherlands) for physicochemical data; Freek van Sambeek for providing Figure 1; Lennart Kleinjans (Laboratory of Microbiology, WUR, The Netherlands) for help with pyrosequencing analysis, Irene Sánchez-Andrea (Laboratory of Microbiology, WUR, The Netherlands) for proof-reading and Katharina Ettwig (Department of Microbiology, Radboud University Nijmegen, The Netherlands) for providing M. oxyfera DNA. We want to thank all anonymous reviewers for valuable contributions. This research is supported by the Dutch Technology Foundation STW (project 10711), which is part of the Netherlands Organization for Scientific Research (NWO), and which is partly funded by the Ministry of Economic Affairs. Research of AJMS is supported by ERC grant (project 323009) and the Gravitation grant (project 024.002.002) of the Netherlands Ministry of Education, Culture and Science and the Netherlands Science Foundation (NWO)

Environmental and vegetation controls on the spatial variability of CH4 emission from wet-sedge and tussock tundra ecosystems in the Arctic

Aims Despite multiple studies investigating the environmental controls on CH4 fluxes from arctic tundra ecosystems, the high spatial variability of CH4 emissions is not fully understood. This makes the upscaling of CH4 fluxes from plot to regional scale, particularly challenging. The goal of this study is to refine our knowledge of the spatial variability and controls on CH4 emission from tundra ecosystems. Methods CH4 fluxes were measured in four sites across a variety of wet-sedge and tussock tundra ecosystems in Alaska using chambers and a Los Gatos CO2 and CH4 gas analyser. Results All sites were found to be sources of CH4, with northern sites (in Barrow) showing similar CH4 emission rates to the southernmost site (ca. 300 km south, Ivotuk). Gross primary productivity (GPP), water level and soil temperature were the most important environmental controls on CH4 emission. Greater vascular plant cover was linked with higher CH4 emission, but this increased emission with increased vascular plant cover was much higher (86 %) in the drier sites, than the wettest sites (30 %), suggesting that transport and/or substrate availability were crucial limiting factors for CH4 emission in these tundra ecosystems. Conclusions Overall, this study provides an increased understanding of the fine scale spatial controls on CH4 flux, in particular the key role that plant cover and GPP play in enhancing CH4 emissions from tundra soils

Stable Carbon and Nitrogen Isotopes in a Peat Profile Are Influenced by Early Stage Diagenesis and Changes in Atmospheric CO2 and N Deposition

In this study, we test whether the δ13C and δ15N in a peat profile are, respectively, linked to the recent dilution of atmospheric δ13CO2 caused by increased fossil fuel combustion and changes in atmospheric δ15N deposition. We analysed bulk peat and Sphagnum fuscum branch C and N concentrations and bulk peat, S. fuscum branch and Andromeda polifolia leaf δ13C and δ15N from a 30-cm hummock-like peat profile from an Aapa mire in northern Finland. Statistically significant correlations were found between the dilution of atmospheric δ13CO2 and bulk peat δ13C, as well as between historically increasing wet N deposition and bulk peat δ15N. However, these correlations may be affected by early stage kinetic fractionation during decomposition and possibly other processes. We conclude that bulk peat stable carbon and nitrogen isotope ratios may reflect the dilution of atmospheric δ13CO2 and the changes in δ15N deposition, but probably also reflect the effects of early stage kinetic fractionation during diagenesis. This needs to be taken into account when interpreting palaeodata. There is a need for further studies of δ15N profiles in sufficiently old dated cores from sites with different rates of decomposition: These would facilitate more reliable separation of depositional δ15N from patterns caused by other processes