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Ninth International Conference on Permafrost ... - IARC Research

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Vegetati<strong>on</strong> Change and Thermokarst Development: Effects <strong>on</strong> Ecosystem Carb<strong>on</strong>Exchange in Upland Tussock TundraJas<strong>on</strong> G. Vogel, Hanna Lee, Christian Trucco, Edward A.G. SchuurDepartment of Botany, University of Florida, Gainesville, FL 32601-8526, USAJames SickmanDepartment of Envir<strong>on</strong>mental Sciences, University of California Riverside, Riverside, CA 92521, USAIntroducti<strong>on</strong>Thermokarst development generally alters the vegetati<strong>on</strong>compositi<strong>on</strong> of an area because of changes in soil temperatureand moisture (Camill et al. 2001). In upland tussock tundra,thermokarst depressi<strong>on</strong>s are wetter and warmer thanundisturbed areas, while areas al<strong>on</strong>g the sides of thermokarstare drier due to drainage (Schuur et al. 2007). The changesin soil climate and vegetati<strong>on</strong> compositi<strong>on</strong> that occur withthermokarst could affect ecosystem C cycling. Plant growth,or net primary productivity (NPP) and microbial respirati<strong>on</strong>(Rm) of organic matter are both affected by soil climate, andit is the balance between these two processes that determinesnet ecosystem exchange (NEE). Vegetati<strong>on</strong> compositi<strong>on</strong> candirectly affect NPP because plant species differ in growthpotential, and can indirectly affect Rm because tissuechemistry str<strong>on</strong>gly influences decompositi<strong>on</strong> rates (Chapin& Shaver 1996). Potential C loss from permafrost soils isimportant to the global C budget because these soils store~1.6 times more C than is currently in the atmosphere(Schuur et al., in press).The objective of this study was to examine how vegetati<strong>on</strong>compositi<strong>on</strong> and NPP, and thermokarst development maybe affecting ecosystem C cycling. In a previous study, wereported that thermokarst depressi<strong>on</strong>s in upland tussocktundra apparently caused the loss of tussock-formingspecies (Eriophorum vaginatum, Carex bigelowii) and again in deciduous shrubs and mesophilic Sphagnum species(Schuur et al. 2007). In this study, we relate these changes invegetati<strong>on</strong> compositi<strong>on</strong>, mortality, and NPP to measurementsof seas<strong>on</strong>al change in ecosystem respirati<strong>on</strong> (Reco), grossprimary productivity (GPP), and net ecosystem exchange(NEE).Materials and MethodsField siteThe study area was in the Eight Mile Lake (EML)watershed in central Alaska. The EML watershed is located7 miles west of the town of Healy, and is near the northend of Denali Nati<strong>on</strong>al Park and Preserve. Osterkampand Romanovsky (1999) have m<strong>on</strong>itored permafrosttemperatures to 27 m since 1985. Between 1990 and 1998the permafrost profile warmed by ~0.7–1.2°C, warmingthat coincided with thermokarst development (Osterkamp2007). Since 1999, permafrost temperatures have stabilizedor slightly decreased (~0.2°C).A natural gradient study was established within 400 m ofthe permafrost m<strong>on</strong>itoring borehole. Three sites were located:“Minimal Thaw,” where surface topography and tussocktundra vegetati<strong>on</strong> appeared little changed by thermokarst;“Moderate Thaw,” where thermokarst development beganabout 15 years ago; and “Extensive Thaw,” where surfacedepressi<strong>on</strong>s are wider and deeper than Moderate Thaw dueto a prol<strong>on</strong>ged period (minimum of 50 years) of thermokarstdevelopment (Schuur et al. 2007).Vegetati<strong>on</strong> samplingVegetati<strong>on</strong> compositi<strong>on</strong> and NPP were sampled in twelve0.7 x 0.7 m quadrats (chamber base) per site that weredistributed in pairs across a 40 m transect The “point frame”method was used to estimate vegetati<strong>on</strong> characteristics,where a thin metal rod is passed vertically through the canopyand the number of intercepti<strong>on</strong> points with vegetati<strong>on</strong> usedto estimate biomass. Site-specific relati<strong>on</strong>ships betweenthe number of point intercepts and vegetati<strong>on</strong> biomasswere developed in 2004 (Schuur et al. 2007) and applied tosurveys in 2004 and 2006. We estimated ground coverage oflive and dead mosses and Eriophorum vaginatum using theline-intercept method. The five dominant moss groups withinthe quadrats were identified, including the area coverage ofdead Sphagnum spp.Ecosystem carb<strong>on</strong> exchangeNEE and Reco were estimated with both an automatic andmanually operated closed chamber system. The chamberswere 0.4 m high and were placed <strong>on</strong> the same 0.7 x 0.7 areasor chamber bases where NPP and plant species compositi<strong>on</strong>were measured. The air inside a chamber was circulatedto an infrared gas analyzer (LI-820) and the rate change inCO 2c<strong>on</strong>centrati<strong>on</strong> recorded <strong>on</strong> either a Campbell CR10x(automatic chamber) or Palm Tungsten C palm pilot (manualchambers). Measurements began in the first few weeks ofMay and c<strong>on</strong>tinued until the end of September. Resp<strong>on</strong>securves of NEE to light and Reco to temperature weredeveloped and growing seas<strong>on</strong> estimates c<strong>on</strong>structed withthese resp<strong>on</strong>se equati<strong>on</strong>s. Gross primary productivity wasestimated as the difference between growing seas<strong>on</strong> NEEand Reco.AnalysesMultiple regressi<strong>on</strong> analysis was used to determine ifvegetati<strong>on</strong> characteristics of a chamber base (proporti<strong>on</strong>of dead moss and NPP of functi<strong>on</strong>al groups) covaried withchamber level variati<strong>on</strong> in growing seas<strong>on</strong> NEE, GPP, andReco. The best parameters for the regressi<strong>on</strong> model wereselected based <strong>on</strong> the maximum coefficient of variati<strong>on</strong>335

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