ALBERT

Description: Contribution of recent photosynthates to methanogenesis and plant-mediated methane (CH4) transport were studied on two dominating vascular plant species – Eriophorum vaginatum and Scheuchzeria palustris – at three microform types (hummocks, lawns and hollows) of a boreal natural minerogenic, oligotrophic fen in Eastern Finland. Measurements of total CH4 flux, isolation of shoots from entire peat and 14C-pulse labeling of mesocosms under controlled conditions allowed estimation of plant-mediated CH4 flux and contribution of recent (14C) photosynthates to total CH4. The obtained results showed (i) CH4 flux increases in the order E. hummocks ≤ E. lawns 〈 S. hollows corresponding to the increasing water table level of the microforms as derived from in situ measurements. (ii) Plant-mediated CH4 flux accounted for 38, 31 and 51 % of total CH4 at E. hummocks, E. lawns and S. hollows, respectively. (iii) Contribution of recent photosynthates to methanogenesis accounted for 0.03 % for E. hummocks, 0.06 % for E. lawns and 0.13 % for S. hollows of assimilated 14C. Thus, S. palustris microsites are characterized by a higher efficiency for transporting CH4 from the peat column to the atmosphere when compared to E. vaginatum of drier lawns and hummocks. Contribution of recent plant photosynthates to methanogenesis was not depended on the amount of plant biomass: smaller S. palustris had higher 14CH4 as compared to larger E. vaginatum. Therefore, for the assessment of CH4 production and emission over meso- and macroscales as well as for the implication and development of C modeling of CH4 fluxes, it is necessary to account for plant species-specific processes including CH4 production, consumption and transportation and the attribution of those species to topographic microforms.

Description: Concentrations of dissolved organic carbon (DOC) in runoff from catchments are often subject to substantial short term variations. The aim of this study was to identify the spatial sources of DOC and the causes for short term variations in runoff from a forested catchment. Furthermore, we investigated the implication of short term variations for the calculation of annual runoff fluxes. High frequency measurements (30 min intervals) of DOC in runoff, of discharge and groundwater table were conducted for one year in the 4.2 km2 forested Lehstenbach catchment, Germany. Riparian wetland soils represent about 30% of the catchment area. The quality of DOC was investigated by three dimensional fluorescence excitation-emission matrices in samples taken from runoff, deep groundwater and shallow groundwater from the riparian wetland soils. The concentrations of DOC in runoff were highly variable at an hourly to daily time scale, ranging from 2.6 mg l−1 to 34 mg l−1 with an annual average of 9.2 mg l−1. The concentrations were positively related to discharge, with a pronounced, counter clockwise hysteresis. Relations of DOC to discharge were steeper in the summer/fall than in the winter/spring season. Dynamics of groundwater table, discharge, DOC concentrations and DOC quality parameters indicated that DOC in runoff originated mainly from the riparian wetland soils, both under low and high flow conditions. The annual export of DOC from the catchment was 84 kg C ha−1 yr−1 when calculated from the high frequency measurements. If the annual export was calculated by simulated random fortnightly samplings, the range was 47 to 124 kg C ha−1 yr−1. Calculations of DOC export fluxes might result in significant errors when based on infrequent (e.g. fortnightly) sampling intervals. Future changes in the precipitation and discharge patterns will influence the DOC dynamics in this catchment, with largest effects in the summer season.

Description: Dissolved organic carbon (DOC) exports from many catchments in Europe and North-America are steadily increasing. Several studies have sought to explain this observation. As possible causes, a decrease in acid rain or sulfate deposition, concomitant reductions in ionic strength and increasing temperatures were identified. DOC often originates from riparian wetlands; but here, despite higher DOC concentrations, ionic strength in pore waters usually exceeds that in surface waters. In the catchment under study, DOC concentrations were synchronous with dissolved iron concentrations in pore and stream water. This study aims at testing the hypothesis that DOC exports are mediated by iron reduction/oxidation cycles. Following the observed hydrographs, δ18O of water, and DOC fluorescence, the wetlands were identified as main source of DOC. Antecedent biogeochemical conditions, i.e. water table levels in the wetlands, influenced the discharge patterns of nitrate, iron, and DOC during an event. The correlation of DOC with pH was positive in pore waters but negative in surface waters; it was negative for DOC with sulfate in pore waters but only weak in surface waters. The positive correlation of DOC with iron was universal for pore and surface water, though. The decline of DOC and iron concentrations in transition from anoxic wetland pore water to oxic stream water suggests a flocculation of DOC with oxidizing iron, leading to a drop in pH in the stream during high DOC fluxes. The pore water did not per se differ in pH. There is thus a need to more thoroughly consider processes of DOC mobilization in wetlands when interpreting DOC exports from catchments. The coupling of DOC with iron fluxes suggested that increased DOC exports could at least in part be caused by increasing activities in iron reduction, possibly due to increases in temperature or wetness of riparian wetlands.

Description: 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 δ13C and δ15N isotope measurements in three bog sites. Peat decomposition generally increased with depth but distinct small scale variation probably caused by environmental changes occurred. C/N ratios varied mostly between 40 and 120 and were significantly correlated (R2 〉 0.55, p 〈 0.01) with FTIR-derived humification indices. The degree of decomposition was lowest at the site with the least sea spray input, while the peat was most decomposed at the driest site with highest sea spray deposition. Decomposition of peat was also advanced near ash layers. Values of δ13C were 26.5 ± 2‰ in the peat and partly related to decomposition indices, while δ15N 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. DOM was enriched in 13C and in 15N relative to the solid phase probably due to multiple microbial modifications and recycling of N in these N-poor environments. In summary, paleoclimatic signals may have influenced decomposition according to depth profiles of C/N ratios, δ13C values, and FTIR spectra, but the study also suggests that decomposition was also influenced by ash layers, sea spray input and other site specific factors.

Description: Climate change induced drying and flooding may alter the redox conditions of organic matter decomposition in peat soils. The seasonal and intermittent changes in pore water solutes (NO3−, Fe2+, SO42−, H2S, acetate) and dissolved soil gases (CO2, O2, CH4, H2) under natural water table fluctuations were compared to the response under a reinforced drying and flooding in fen peats. Oxygen penetration during dryings led to CO2 and CH4 degassing and to a regeneration of dissolved electron acceptors (NO3−, Fe3+ and SO42−). Drying intensity controlled the extent of the electron acceptor regeneration. Iron was rapidly reduced and sulfate pools ~ 1 mmol L−1 depleted upon rewetting and CH4 did not substantially accumulate until sulfate levels declined to ~ 100 μmoll−1. The post-rewetting recovery of soil methane concentrations to levels ~ 80 μmoll−1 needed 40–50 days after natural drought. This recovery was prolonged after experimentally reinforced drought. A greater regeneration of electron acceptors during drying was not related to prolonged methanogenesis suppression after rewetting. Peat compaction, solid phase content of reactive iron and total reduced inorganic sulfur and organic matter content controlled oxygen penetration, the regeneration of electron acceptors and the recovery of CH4 production, respectively. Methane production was maintained despite moderate water table decline of 20 cm in denser peats. Flooding led to accumulation of acetate and H2, promoted CH4 production and strengthened the co-occurrence of iron and sulfate reduction and methanogenesis. Mass balances during drying and flooding indicated that an important fraction of the electron flow must have been used for the generation and consumption of electron acceptors in the solid phase or other mechanisms. In contrast to flooding, dry-wet cycles negatively affect methane production on a seasonal scale but this impact might strongly depend on drying intensity and on the peat matrix, whose structure and physical properties influence moisture content.

Description: Peat humification or decomposition is a frequently used proxy to extract past time changes in hydrology and climate from peat bogs. During the past century several methods to determine changes in peat decomposition have been introduced. Most of these methods are operationally defined only and the chemical changes underlying the decomposition process are often poorly understood and lack validation. Due to the chemically undefined nature of many humification analyses the comparison of results obtained by different methods is difficult if not misleading. In this study we compared changes in peat decomposition in cores of two peat bogs (Königsmoor (KK), Kleines Rotes Bruch, KRB) from the Harz Mountains (Germany) using C / N ratios, Fourier Transform Infrared spectra absorption (FTIR) intensities, Rock Eval® oxygen- and hydrogen indices, δ13C and δ15N isotopic signatures and UV-absorption of NaOH peat extracts. In addition, one of the cores was analysed for changes in the peat's molecular composition using pyrolysis gas chromatography mass spectrometry (pyrolysis-GC-MS). Records of decomposition proxies show similar historical development at both sites, indicating external forcing such as climate as controlling process. Moreover, all decomposition proxies except UV-ABS and δ15N isotopes show similar patterns in their records and thus reflect in different extents signals of decomposition. Pyrolysis-GC-MS analyses of the KK core reveal that changes in peat molecular chemistry are mainly attributed to decomposition processes and to a lesser extend to changes in vegetation. Changes in the abundance of molecular compounds indicate that peat decomposition in the KK bog is mainly characterized by preferential decomposition of phenols and polysaccharides and relative enrichment of aliphatics during drier periods. Enrichment of lignin and other aromatics during decomposition was also observed but showed less variation, and presumably reflects changes in vegetation associated to changes in hydrology of the bogs. Significant correlations with polysaccharide and aliphatic pyrolysis products were found for C / N ratios, FTIR-band intensities and for hydrogen index values, supporting that these decomposition indices provide reasonable information despite their bulk nature. Correlation with oxygen index values and δ13C was weaker assumingly indicating carboxylation of the peat during drier periods and enrichment of isotopically lighter peat components during decomposition, respectively. FTIR, C / N ratio, Pyrolysis-GC-MS analyses and Rock Eval hydrogen indices appear to reflect mass loss and related changes in the molecular peat composition during mineralization best. Different to the other investigated proxies, Pyrolysis-GC-MS and FTIR analyses allow disentangling decomposition processes and vegetation changes. UV-ABS measurements of alkaline peat extracts show only weak correlation with other decomposition proxiesas they mainly reflect the formation of humic acids through humifcation and to a~lesser extend mass loss during mineralization.

Description: Plant-mediated methane (CH4) transport and the contribution of recent photosynthates to methanogenesis were studied on two dominating vascular plant species – Eriophorum vaginatum and Scheuchzeria palustris – at three types of microrelief forms (hummocks – E. hummocks, lawns – E. lawns and hollows – S. hollows) of a boreal natural minerogenic, oligotrophic fen in Eastern Finland. 14C-pulse labeling of mesocosms with shoots isolated from entire belowground peat under controlled conditions allowed estimation of plant-mediated CH4 flux and contribution of recent (14C) photosynthates to total CH4. The results showed (i) CH4 flux increased in the order E. hummocks ≤ E. lawns 〈 S. hollows corresponding to the increasing water table level at the relief microforms as adjusted to field conditions. (ii) Plant-mediated CH4 flux accounted for 38, 31 and 51 % of total CH4 at E. hummocks, E. lawns and S. hollows, respectively. (iii) Contribution of recent photosynthates to methanogenesis accounted for 0.03 % for E. hummocks, 0.06 % for E. lawns and 0.13 % for S.hollows of assimilated 14C. Thus, microsites with S. palustris were characterized by higher rates of transported CH4 from the peat column to the atmosphere when compared to E. vaginatum of drier lawns and hummocks. Contribution of recent photosynthates to methanogenesis was dependent on the plant biomass within-species level (E. vaginatum at hummocks and lawns) but was not observed between species: smaller S. palustris had higher flux of 14CH4 as compared to larger E. vaginatum. Therefore, for the assessment of CH4 dynamics over meso- and macroscale as well as for the implication and development of the modeling of CH4 fluxes, it is necessary to account for plant species-specific differences in CH4 production, consumption and transport and the attribution of those species to topographic forms of microrelief.