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Carbon (C) modeling and carbon dioxide (CO2) flux measurements in peatlands are dependent on the distribution and productivity of vegetation in a system with a high degree of spatial variability, often linked to the position of the water table. We tested the hypothesis that at a fine-scale (tens of metres) water table position exerts a strong control on species abundance, plant biomass, particularly photosynthetically active tissues, leaf area index (LAI), and areal foliar N and chlorophyll at Mer Bleue, a cool temperate peatland in eastern Canada. Total aboveground biomass ranged from 147 to 1011 g·m–2, with shrubs contributing between 42% and 72% of the total in the transects. We found significant (P < 0.05) positive relationships between foliar and total vascular plant biomass and mean water table position, and significant decreases in the shrub foliar:woody biomass ratio and moss biomass with a lower water table. However, there was no significant relationship between water table position and photosynthetically active tissues (vascular plant leaves and moss capitulum), ranging from 114 to 672 g·m–2) and the areal mass of N in these tissues, ranging from 1.5 to 6.7 g·m–2. Multivariate analyses of vegetation and environmental data showed that species distribution could be explained by both water table and chemistry gradients and that unimodal rather than linear responses best described the species and water table relationships. LAI ranged from 0.1 to over 3 and was correlated with both water table position and with vascular foliar biomass. Percent cover of shrubs was correlated with foliar biomass and LAI. Our results suggest that the less labour-intensive estimates of percent cover can be used to predict the vascular plant foliar biomass and LAI measurements. The lack of relationship between photosynthetically active tissues, tissue N concentrations, and water table may also explain the surprising lack of spatial variability in peak growing season eddy flux net ecosystem CO2 exchange in three different areas of the peatland. [ABSTRACT FROM AUTHOR]

Climate change scenarios suggest that northern peatlands could become drier. To address the type and magnitude of vegetation change associated with persistent drying, we studied changes in biomass and leaf area index following drainage 85 years previously of a bog, using destructive sampling, allometric relationships, and optical measurements. Our results show a 10-fold increase in aboveground biomass between the reference site and the most severely drained site, resulting from the growth of a tree layer. The total leaf biomass increased slightly as a result of drainage, thus an increase in woody biomass was the main cause of the increase in aboveground biomass. Leaf area index approximately tripled in sites where trees grew. Sphagnum L. moss biomass decreased from 120 g·m−2 at the reference site (20% of all aboveground biomass) to 8 g·m−2 under the tree canopy (<1% of all aboveground biomass). The percentage of deciduous shrubs increased from 3% of the total shrub biomass in the reference site to 72% in the most severely drained site. Our results show that lowering the water table of a bog can have a profound effect on vegetation but the net effect of these changes on the role of the peatland as a carbon sink remains difficult to assess. [ABSTRACT FROM AUTHOR]

We compared the amount and composition of different aboveground biomass (BM) fractions of four mires with their net ecosystem CO2 exchange (NEE) measured by eddy covariance. We found clear differences in response of green biomass (GBM) of plant functional types (PFTs) to water table (WT), which resulted in larger spatial variation in GBM within a mire than variation between mires. GBM varied between mires from 126 ± 7 to 336 ± 16 g·m-2 (mean ± SE), while within mire variation at largest was from 157 ± 17 to 488 ± 20 g·m-2 (mean ± SE). GBM of dominant PFTs appeared to be better in explaining the peak growing season NEE than the total BM or GBM of a mire. The differences in photosynthetic capacity between PTFs had a major role, and thus a smaller GBM with different species composition could result in higher NEE than larger GBM. Vascular plant GBM, especially that of sedges, appeared to have a high impact on NEE. Eleven PFTs, defined here, appeared to capture well the internal variation within mires, and the differences in GBM between communities were explained by the water table response of PFTs. Our results suggest the use of photosynthesizing BM, separated into PFTs, in modelling ecosystem carbon exchange instead of using just total BM. [ABSTRACT FROM AUTHOR]