Abstract
Dominant plant functional groups (PFGs) found in boreal rich fens include sedges, grasses, horsetails, and cinquefoils (obligate wetland shrubs). Precipitation regime shift and permafrost thaw due to climate change will likely trigger changes in fen plant community structure through shifts in these PFGs, and it is thus crucial to understand how these PFGs will impact carbon cycling and greenhouse gas dynamics to predict and model peatland-climate feedbacks. In this study, we detail the above and belowground effects of these PFGs on aspects of carbon cycling using a mesocosm approach. We hypothesized that PFGs capable of aerating the rhizosphere (sedges, horsetails, and grasses) would oxidize the belowground environment supporting higher redox potentials, a favorable environment for decomposition, and higher CO2:CH4 in pore water and gas efflux measurements than PFGs lacking aerenchyma (cinquefoil, unplanted control). Overall, sedges, horsetail and grasses had an oxidizing effect on rhizosphere pore water chemistry, producing an environment more favorable for methanotrophy during the growing season, as supported by an approximate isotopic enrichment of pore water methane (δ13CH4) by 5‰, and isotopic depletion in pore water carbon dioxide (δ13CO2) by 10‰, relative to cinquefoil treatments. Cinquefoil and unplanted control treatments fostered a reducing environment more favorable for methanogenesis. In addition, cinquefoil appeared to slow decomposition in comparison with the other PFGs. These findings, paired with PFG effects on oxidation–reduction potential and CO2 and CH4 production, point to the ability of rich fen plant communities to moderate biogeochemistry, specifically carbon cycling, in response to changing climatic conditions.
Similar content being viewed by others
Abbreviations
- APEX:
-
Alaska peatland experiment
- BIX:
-
Biological index
- CH4 :
-
Methane
- CO2 :
-
Carbon dioxide
- DOC:
-
Dissolved organic carbon
- DOM:
-
Dissolved organic matter
- ESC:
-
Electron shuttling capacity
- HIX:
-
Humification index
- NDVI:
-
Normalized difference vegetation index
- PFG:
-
Plant functional group
- Sr:
-
Spectral ratio
- SUVA:
-
Specific ultraviolet absorbance
- TI:
-
Tryptophan index
- TN:
-
Total nitrogen
References
Agethen S, Sander M, Waldemer C, Knorr K-H (2018) Plant rhizosphere oxidation reduces methane production and emission in rewetted peatlands. Soil Biol Biochem 125:125–135
Ali P, Chen Y-F, Sargsyan E (2014) Bioactive molecules of herbal extracts with anti-infective and wound healing properties. In: Kon K, Rai M (eds) Microbiology for surgical infections. Academic Press, Amsterdam, pp 205–220
Asada T, Warner BG, Banner A (2003) Growth of mosses in relation to climate factors in a hypermaritime coastal peatland in British Columbia, Canada. Bryologist 106(4):516–528
Avagyan A, Runkle BR, Kutzbach L (2014) Application of high-resolution spectral absorbance measurements to determine dissolved organic carbon concentration in remote areas. J Hydrol 517:435–446
Basiliko N, Knowles R, Moore TR (2004) Roles of moss species and habitat in methane consumption potential in a northern peatland. Wetlands 24(1):178
Basiliko N, Blodau C, Roehm C, Bengtson P, Moore TR (2007) Regulation of decomposition and methane dynamics across natural, commercially mined, and restored northern peatlands. Ecosystems 10(7):1148–1165
Bauer M, Heitmann T, Macalady DL, Blodau C (2007) Electron transfer capacities and reaction kinetics of peat dissolved organic matter. Environ Sci Technol 41(1):139–145
Berger S, Praetzel L, Goebel M, Blodau C, Knorr K-H (2018) Response of carbon cycling in a peatland subjected to long-term nutrient input and altered hydrologic conditions. In: EGU general assembly conference abstracts, vol 20, p 7225
Bier AW (2009) Introduction to oxidation reduction potential measurement. Hach Company, Lit, Loveland, CO
Blodau C, Bauer M, Regenspurg S, Macalady D (2009) Electron accepting capacity of dissolved organic matter as determined by reaction with metallic zinc. Chem Geol 260(3–4):186–195
Brancaleoni L, Gerdol R (2014) Habitat-dependent interactive effects of a heatwave and experimental fertilization on the vegetation of an alpine mire. J Veg Sci 25(2):427–438
Carroll P, Crill P (1997) Carbon balance of a temperate poor fen. Global Biogeochem Cycles 11(3):349–356
Chanton JP, Bauer JE, Glaser PA, Siegel DI, Kelley CA, Tyler SC, Romanowicz EH, Lazrus A (1995) Radiocarbon evidence for the substrates supporting methane formation within northern Minnesota peatlands. Geochim Cosmochim Acta 59(17):3663–3668
Chanton J, Glaser P, Chasar L, Burdige DJ, Hines M, Siegel D, Tremblay L, Cooper W (2008) Radiocarbon evidence for the importance of surface vegetation on fermentation and methanogenesis in contrasting types of boreal peatlands. Global Biogeochem Cycles. https://doi.org/10.1029/2008GB003274
Chapin FS III, Bret-Harte MS, Hobbie SE, Zhong H (1996) Plant functional types as predictors of transient responses of arctic vegetation to global change. J Veg Sci 7(3):347–358
Chasar LS, Chanton JP, Glaser PH, Siegel DI (2000) Methane concentration and stable isotope distribution as evidence of rhizospheric processes: comparison of a fen and bog in the Glacial Lake Agassiz peatland complex. Ann Bot 86(3):655–663
Cheng W, Kuzyakov Y (2005) Root effects on soil organic matter decomposition. Roots and soil management: interactions between roots and the soil. American Society of Agronomy Inc, Madison, WI, pp 119–143
Churchill AC, Turetsky MR, McGuire AD, Hollingsworth TN (2014) Response of plant community structure and primary productivity to experimental drought and flooding in an Alaskan fen. Can J For Res 45(2):185–193
Conrad R (1999) Contribution of hydrogen to methane production and control of hydrogen concentrations in methanogenic soils and sediments. FEMS Microbiol Ecol 28(3):193–202
Crum H, Planisek S (1992) A focus on peatlands and peat mosses. University of Michigan Press, Ann Arbor, MI
De Deyn GB, Cornelissen JH, Bardgett RD (2008) Plant functional traits and soil carbon sequestration in contrasting biomes. Ecol Lett 11(5):516–531
De Haan H, De Boer T (1987) Applicability of light absorbance and fluorescence as measures of concentration and molecular size of dissolved organic carbon in humic Lake Tjeukemeer. Water Res 21(6):731–734
Dieleman CM, Branfireun BA, McLaughlin JW, Lindo Z (2015) Climate change drives a shift in peatland ecosystem plant community: implications for ecosystem function and stability. Glob Change Biol 21(1):388–395
Dieleman CM, Branfireun BA, Lindo Z (2017) Northern peatland carbon dynamics driven by plant growth form—the role of graminoids. Plant Soil 415(1–2):25–35
Dinsmore KJ, Skiba UM, Billett MF, Rees RM (2009) Effect of water table on greenhouse gas emissions from peatland mesocosms. Plant Soil 318(1–2):229
Elizabeth Corbett J, Burdige DJ, Tfaily MM, Dial AR, Cooper WT, Glaser PH, Chanton JP (2013) Surface production fuels deep heterotrophic respiration in northern peatlands. Global Biogeochem Cycles 27(4):1163–1174
Estop-Aragonés C, Knorr K-H, Blodau C (2013) Belowground in situ redox dynamics and methanogenesis recovery in a degraded fen during dry-wet cycles and flooding. Biogeosciences 10(1):421
Fan Z, David McGuire A, Turetsky MR, Harden JW, Michael Waddington J, Kane ES (2013) The response of soil organic carbon of a rich fen peatland in interior Alaska to projected climate change. Glob Change Biol 19(2):604–620
Fellman JB, Miller MP, Cory RM, D’Amore DV, White D (2009) Characterizing dissolved organic matter using PARAFAC modeling of fluorescence spectroscopy: a comparison of two models. Environ Sci Technol 43(16):6228–6234
Gadgil RL, Gadgil PD (1971) Mycorrhiza and litter decomposition. Nature 233(5315):133
Gadgil PD, Gadgil RL (1975) Suppression of litter decomposition by mycorrhizal roots of Pinus radiata. Forest Research Institute, New Zealand Forest Service, Rotorua
Glaser PH, Chanton JP (2009) Methane accumulation and release from deep peat: measurements, conceptual models, and biogeochemical significance. In: Baird AJ, Belyea LR, Comas X, Reeve AS, Slater LD (eds) Carbon cycling in northern peatlands, vol 184. American Geophysical Union, Washington, DC, pp 145–158
Gorham E (1991) Northern peatlands: role in the carbon cycle and probable responses to climatic warming. Ecol Appl 1(2):182–195
Hauke RL (1979) A taxonomic monograph of Equisetum subgenus Equisetum. Nova Hedwigia 385–456
Heitmann T, Goldhammer T, Beer J, Blodau C (2007) Electron transfer of dissolved organic matter and its potential significance for anaerobic respiration in a northern bog. Glob Change Biol 13(8):1771–1785
Helms JR, Stubbins A, Ritchie JD, Minor EC, Kieber DJ, Mopper K (2008) Absorption spectral slopes and slope ratios as indicators of molecular weight, source, and photobleaching of chromophoric dissolved organic matter. Limnol Oceanogr 53(3):955–969
Hinzman LD, Bettez ND, Bolton WR, Chapin FS, Dyurgerov MB, Fastie CL, Griffith B, Hollister RD, Hope A, Huntington HP, Jensen AM, Jia GJ, Jorgenson T, Kane DL, Klein DR, Kofinas G, Lynch AH, Lloyd AH, McGuire AD, Nelson FE, Oechel WC, Osterkamp TE, Racine CH, Romanovsky VE, Stone RS, Stow DA, Sturm M, Tweedie CE, Vourlitis GL, Walker MD, Walker DA, Webber PJ, Welker JM, Winker KS, Yoshikawa K (2005) Evidence and implications of recent climate change in northern Alaska and other arctic regions. Clim Change 72(3):251–298
Hinzman LD, Viereck LA, Adams PC, Romanovsky VE, Yoshikawa K (2006) Climate and permafrost dynamics of the Alaskan boreal forest. In: Chapin FS, Oswood MW, Van Cleve K, Viereck LA, Verbyla DL (eds) Alaska’s changing Boreal forest. Oxford University Press Inc, New York, pp 39–61
Hobbie EA, Ouimette AP, Schuur EA, Kierstead D, Trappe JM, Bendiksen K, Ohenoja E (2013) Radiocarbon evidence for the mining of organic nitrogen from soil by mycorrhizal fungi. Biogeochemistry 114(1–3):381–389
Holzapfel-Pschorn A, Conrad R, Seiler W (1986) Effects of vegetation on the emission of methane from submerged paddy soil. Plant Soil 92(2):223–233
Hribljan J, Kane E, Chimner R (2017) Implications of altered hydrology for substrate quality and trace gas production in a poor fen peatland. Soil Sci Soc Am J 81(3):633–646
Huguet A, Vacher L, Relexans S, Saubusse S, Froidefond JM, Parlanti E (2009) Properties of fluorescent dissolved organic matter in the Gironde Estuary. Org Geochem 40(6):706–719
Jassey VE, Chiapusio G, Binet P, Buttler A, Laggoun-Défarge F, Delarue F, Bernard N, Mitchell EA, Toussaint ML, Francez AJ (2013) Above-and belowground linkages in Sphagnum peatland: climate warming affects plant-microbial interactions. Glob Change Biol 19(3):811–823
Kane ES, Chivers MR, Turetsky MR, Treat CC, Petersen DG, Waldrop M, Harden JW, McGuire AD (2013) Response of anaerobic carbon cycling to water table manipulation in an Alaskan rich fen. Soil Biol Biochem 58:50–60
Kaye JP, Hart SC (1997) Competition for nitrogen between plants and soil microorganisms. Trends Ecol Evol 12(4):139–143
Keller JK, Bridgham SD (2007) Pathways of anaerobic carbon cycling across an ombrotrophic-minerotrophic peatland gradient. Limnol Oceanogr 52(1):96–107
Keller JK, Takagi KK (2013) Solid-phase organic matter reduction regulates anaerobic decomposition in bog soil. Ecosphere 4(5):1–12
Keller JK, Weisenhorn PB, Megonigal JP (2009) Humic acids as electron acceptors in wetland decomposition. Soil Biol Biochem 41(7):1518–1522
King JY, Reeburgh WS, Regli SK (1998) Methane emission and transport by arctic sedges in Alaska: results of a vegetation removal experiment. J Geophys Res Atmos 103(D22):29083–29092
Klupfel L, Piepenbrock A, Kappler A, Sander M (2014) Humic substances as fully regenerable electron acceptors in recurrently anoxic environments. Nat Geosci 7(3):195–200
Knorr K-H, Glaser B, Blodau C (2008) Fluxes and 13C isotopic composition of dissolved carbon and pathways of methanogenesis in a fen soil exposed to experimental drought. Biogeosciences 5:1457–1473
Koelbener A, Ström L, Edwards PJ, Olde Venterink H (2009) Plant species from mesotrophic wetlands cause relatively high methane emissions from peat soil. Plant Soil 326(1):147–158
Kothawala DN, Von Wachenfeldt E, Koehler B, Tranvik LJ (2012) Selective loss and preservation of lake water dissolved organic matter fluorescence during long-term dark incubations. Sci Total Environ 433:238–246
Kuiper JJ, Mooij WM, Bragazza L, Robroek BJ (2014) Plant functional types define magnitude of drought response in peatland CO2 exchange. Ecology 95(1):123–131
Kytoviita MM, Ruotsalainen AL (2007) Mycorrhizal benefit in two low arctic herbs increases with increasing temperature. Am J Bot 94(8):1309–1315
Laiho R, Vasander H, Penttilä T, Laine J (2003) Dynamics of plant-mediated organic matter and nutrient cycling following water-level drawdown in boreal peatlands. Glob Biogeochem Cycles. https://doi.org/10.1029/2002GB002015
Landhäusser SM, Lieffers VJ (1994) Competition between Calamagrostis canadensis and Epilobium angustifolium under different soil temperature and nutrient regimes. Can J For Res 24(11):2244–2250
Lara MJ, Genet H, McGuire AD, Euskirchen ES, Zhang Y, Brown DR, Jorgenson MT, Romanovsky V, Breen A, Bolton WR (2016) Thermokarst rates intensify due to climate change and forest fragmentation in an Alaskan boreal forest lowland. Glob Change Biol 22(2):816–829
Lau MP, Sander M, Gelbrecht J, Hupfer M (2015) Solid phases as important electron acceptors in freshwater organic sediments. Biogeochemistry 123(1–2):49–61
Lawaetz AJ, Stedmon C (2009) Fluorescence intensity calibration using the Raman scatter peak of water. Appl Spectrosc 63(8):936–940
Lenth RV (2016) Least-squares means: the R package lsmeans. J Stat Softw 69(1):1–33
Lindahl BD, Tunlid A (2015) Ectomycorrhizal fungi–potential organic matter decomposers, yet not saprotrophs. New Phytol 205(4):1443–1447
Marsh AS, Arnone JA, Bormann BT, Gordon JC (2000) The role of Equisetum in nutrient cycling in an Alaskan shrub wetland. J Ecol 88(6):999–1011
Mary B, Fresneau C, Morel J, Mariotti A (1993) C and N cycling during decomposition of root mucilage, roots and glucose in soil. Soil Biol Biochem 25(8):1005–1014
McConnell NA, Turetsky MR, David McGuire A, Kane ES, Waldrop MP, Harden JW (2013) Controls on ecosystem and root respiration across a permafrost and wetland gradient in interior Alaska. Environ Res Lett 8(4):045029
McPartland MY, Kane ES, Falkowski MJ, Kolka R, Turetsky MR, Palik B, Montgomery RA (2019) The response of boreal peatland community composition and NDVI to hydrologic change, warming and elevated carbon dioxide. Glob Change Biol 25(1):93–107
Miller MP, McKnight DM, Cory RM, Williams MW, Runkel RL (2006) Hyporheic exchange and fulvic acid redox reactions in an alpine stream/wetland ecosystem, Colorado Front Range. Environ Sci Technol 40(19):5943–5949
Minkkinen K, Vasander H, Jauhiainen S, Karsisto M, Laine J (1999) Post-drainage changes in vegetation composition and carbon balance in Lakkasuo mire, Central Finland. Plant Soil 207(1):107–120
Noyce GL, Varner RK, Bubier JL, Frolking S (2014) Effect of Carex rostrata on seasonal and interannual variability in peatland methane emissions. J Geophys Res Biogeosci 119(1):24–34
Ohno T (2002) Fluorescence inner-filtering correction for determining the humification index of dissolved organic matter. Environ Sci Technol 36(4):742–746
Olefeldt D, Euskirchen ES, Harden J, Kane E, McGuire AD, Waldrop MP, Turetsky MR (2017) A decade of boreal rich fen greenhouse gas fluxes in response to natural and experimental water table variability. Glob Change Biol 23(6):2428–2440
Parlanti E, Wörz K, Geoffroy L, Lamotte M (2000) Dissolved organic matter fluorescence spectroscopy as a tool to estimate biological activity in a coastal zone submitted to anthropogenic inputs. Org Geochem 31(12):1765–1781
Pedrotti E, Rydin H, Ingmar T, Hytteborn H, Turunen P, Granath G (2014) Fine-scale dynamics and community stability in boreal peatlands: revisiting a fen and a bog in Sweden after 50 years. Ecosphere 5(10):1–24
Pinheiro J, Bates D, DebRoy S, Sarkar D (2014) R core team (2014) nlme: linear and nonlinear mixed effects models. R package version 3.1-117. http://CRAN.R-project.org/package=nlme
Potvin LR, Kane ES, Chimner RA, Kolka RK, Lilleskov EA (2014) Effects of water table position and plant functional group on plant community, aboveground production, and peat properties in a peatland mesocosm experiment (PEATcosm). Plant Soil 387(1):277–294
Radu DD, Duval TP (2018) Precipitation frequency alters peatland ecosystem structure and CO2 exchange: contrasting effects on moss, sedge, and shrub communities. Glob Change Biol 24(5):2051–2065
Read DJ, Leake JR, Perez-Moreno J (2004) Mycorrhizal fungi as drivers of ecosystem processes in heathland and boreal forest biomes. Can J Bot 82(8):1243–1263
Romanowicz KJ, Kane ES, Potvin LR, Daniels AL, Kolka RK, Lilleskov EA (2015) Understanding drivers of peatland extracellular enzyme activity in the PEATcosm experiment: mixed evidence for enzymic latch hypothesis. Plant Soil 397(1):371–386
Rydin H, Jeglum JK (2013) The biology of peatlands, 2nd edn. Oxford University Press, New York
Schaepman-Strub G, Limpens J, Menken M, Bartholomeus H, Schaepman M (2009) Towards spatial assessment of carbon sequestration in peatlands: spectroscopy based estimation of fractional cover of three plant functional types. Biogeosciences 6(2):275–284
Schütte UM, Henning JA, Ye Y, Bowling A, Ford J, Genet H, Waldrop M, Turetsky MR, White JR, Bever JD (2019) Effect of permafrost thaw on plant and soil fungal community in a boreal forest: does fungal community change mediate plant productivity response? J Ecol 107:1737–1752
Sowers TD, Stuckey JW, Sparks DL (2018) The synergistic effect of calcium on organic carbon sequestration to ferrihydrite. Geochem Trans 19(1):4
Stedmon CA, Bro R (2008) Characterizing dissolved organic matter fluorescence with parallel factor analysis: a tutorial. Limnol Oceanogr 6(11):572–579
Steward BC, Kunkel KE, Stevens LE, Sun L, Walsch JE (2013) Regional climate trends and scenarios for the US national climate assessment. NOAA technical report NESDIS 142-7 www.nesdis.noaa.gov/content/technical-reports
Strack M, Waddington J, Rochefort L, Tuittila E-S (2006a) Response of vegetation and net ecosystem carbon dioxide exchange at different peatland microforms following water table drawdown. J Geophys Res. https://doi.org/10.1029/2005JG000145
Strack M, Waller MF, Waddington JM (2006b) Sedge succession and peatland methane dynamics: a potential feedback to climate change. Ecosystems 9(2):278–287
Strack M, Mwakanyamale K, Hassanpour Fard G, Bird M, Bérubé V, Rochefort L (2017) Effect of plant functional type on methane dynamics in a restored minerotrophic peatland. Plant Soil 410(1):231–246
Sudová R, Vosátka M (2008) Effects of inoculation with native arbuscular mycorrhizal fungi on clonal growth of Potentilla reptans and Fragaria moschata (Rosaceae). Plant Soil 308(1):55–67
Throckmorton HM, Heikoop JM, Newman BD, Altmann GL, Conrad MS, Muss JD, Perkins GB, Smith LJ, Torn MS, Wullschleger SD (2015) Pathways and transformations of dissolved methane and dissolved inorganic carbon in Arctic tundra watersheds: evidence from analysis of stable isotopes. Glob Biogeochem Cycles 29(11):1893–1910
Treseder KK, Turner KM, Mack MC (2007) Mycorrhizal responses to nitrogen fertilization in boreal ecosystems: potential consequences for soil carbon storage. Glob Change Biol 13(1):78–88
Turetsky MR, Crow SE, Evans RJ, Vitt DH, Wieder RK (2008) Trade-offs in resource allocation among moss species control decomposition in boreal peatlands. J Ecol 96(6):1297–1305
Turetsky MR, Bond-Lamberty B, Euskirchen E, Talbot J, Frolking S, McGuire AD, Tuittila ES (2012) The resilience and functional role of moss in boreal and arctic ecosystems. New Phytol 196(1):49–67
Turetsky MR, Kotowska A, Bubier J, Dise NB, Crill P, Hornibrook ER, Minkkinen K, Moore TR, Myers-Smith IH, Nykänen H (2014) A synthesis of methane emissions from 71 northern, temperate, and subtropical wetlands. Glob Change Biol 20(7):2183–2197
Usda N (2018) The PLANTS database. National Plant Data Team, Greensboro, NC
Valentine DW, Holland EA, Schimel DS (1994) Ecosystem and physiological controls over methane production in northern wetlands. J Geophys Res Atmos 99(D1):1563–1571
Veverica TJ, Kane ES, Marcarelli AM, Green SA (2016) Ionic liquid extraction unveils previously occluded humic-bound iron in peat soil pore water. Soil Sci Soc Am J 80(3):771–782
Vile MA, Bridgham SD, Wieder RK, Novák M (2003) Atmospheric sulfur deposition alters pathways of gaseous carbon production in peatlands. Glob Biogeochem Cycles. https://doi.org/10.1029/2002GB001966
Vitt DH, Halsey LA, Bauer IE, Campbell C (2000) Spatial and temporal trends in carbon storage of peatlands of continental western Canada through the Holocene. Can J Earth Sci 37(5):683–693
Walpen N, Getzinger GJ, Schroth MH, Sander M (2018) Electron-donating phenolic and electron-accepting quinone moieties in peat dissolved organic matter: quantities and redox transformations in the context of peat biogeochemistry. Environ Sci Technol 52(9):5236–5245
Ward SE, Bardgett RD, McNamara NP, Ostle NJ (2009) Plant functional group identity influences short-term peatland ecosystem carbon flux: evidence from a plant removal experiment. Funct Ecol 23(2):454–462
Ward SE, Orwin KH, Ostle NJ, Briones MJI, Thomson BC, Griffiths RI, Oakley S, Quirk H, Bardgett RD (2015) Vegetation exerts a greater control on litter decomposition than climate warming in peatlands. Ecology 96(1):113–123
Weishaar JL, Aiken GR, Bergamaschi BA, Fram MS, Fujii R, Mopper K (2003) Evaluation of specific ultraviolet absorbance as an indicator of the chemical composition and reactivity of dissolved organic carbon. Environ Sci Technol 37(20):4702–4708
Weltzin JF, Harth C, Bridgham SD, Pastor J, Vonderharr M (2001) Production and microtopography of bog bryophytes: response to warming and water-table manipulations. Oecologia 128(4):557–565
Whiting GJ, Chanton JP (1992) Plant-dependent CH4 emission in a subarctic Canadian fen. Glob Biogeochem Cycles 6(3):225–231
Wickham H (2016) ggplot2: elegant graphics for data analysis. Springer, Berlin
Wiedermann MM, Kane ES, Potvin LR, Lilleskov EA (2017) Interactive plant functional group and water table effects on decomposition and extracellular enzyme activity in Sphagnum peatlands. Soil Biol Biochem 108:1–8
Yu ZC (2012) Northern peatland carbon stocks and dynamics: a review. Biogeosciences 9(10):4071–4085
Zalman C, Keller JK, Tfaily M, Kolton M, Pfeifer-Meister L, Wilson RM, Lin X, Chanton J, Kostka JE, Gill A, Finzi A, Hopple AM, Bohannan BJM, Bridgham SD (2018) Small differences in ombrotrophy control regional-scale variation in methane cycling among Sphagnum-dominated peatlands. Biogeochemistry 139(2):155–177
Acknowledgements
The University of Alaska-Fairbanks Institute of Arctic Biology and the Bonanza Creek Long Term Experimental Research station provided both lab space, equipment, and time to this project. Emilia Grzesik, Devan Bruce, and Jamie Ramsey contributed invaluable fieldwork; fluorometric data processing relied upon Matlab and R code written by Karl Meingast. The authors wholeheartedly thank associate editor Sharon Billings and an anonymous reviewer for their time reviewing this article. This project was funded by National Science Foundation grant DEB LTREB 1354370. The APEX site has been supported by National Science Foundation Grants (DEB-0425328, DEB-0724514 and DEB-0830997).
Author information
Authors and Affiliations
Corresponding author
Ethics declarations
Conflict of interest
The authors declare that they have no conflict of interest.
Additional information
Responsible Editor: Sharon A. Billings.
Publisher's Note
Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.
Rights and permissions
About this article
Cite this article
Rupp, D., Kane, E.S., Dieleman, C. et al. Plant functional group effects on peat carbon cycling in a boreal rich fen. Biogeochemistry 144, 305–327 (2019). https://doi.org/10.1007/s10533-019-00590-5
Received:
Accepted:
Published:
Issue Date:
DOI: https://doi.org/10.1007/s10533-019-00590-5