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Effects of allochthonous organic matter and iron on plankton community functioning and annual carbon cycling in a subarctic estuary under winter conditions.Verheijen, Hendricus January 2016 (has links)
High winter respiration has been observed in a subarctic estuary with high levels of organic matter inputs, while winter is generally thought to be a non-productive season. We constructed an oxygen and carbon budget of the system to validate the high respiration rate, including the resulting low production-to-respiration ratio, and to identify important carbon and energy sources. Measurement data of production and respiration parameters from running monitoring programs were used. Furthermore, we set up a microcosm experiment in order to study effects of iron increases by riverine organic matter inputs. The carbon balance of this subarctic estuary shows a small deficiency of carbon on an annual basis, but is able to explain how winter respiration is fueled by carbon fixed in the autumnal season and inputs of riverine material. Also, the balance calculation was able to predict oxygen deficiencies on a seasonal basis. The effect of riverine organic matter on biological activity was clearly present, but iron did not appear to affect responses in primary or secondary producers. Additional studies will be needed to fully understand the role of iron additions to marine microbial communities, particularly focusing on fractioning of iron and organic matter species.
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Interactions between nitrogen fixation and methane cycling in boreal peat bogsWarren, Melissa 08 June 2015 (has links)
Microbial nitrogen (N2) fixation supplies important nitrogen inputs to boreal peatlands, extremely oligotrophic ecosystems dominated by Sphagnum mosses. In this study, we coupled major and trace nutrient analyses and rate measurements to characterize interactions between N2 fixation and CH4 cycling at the S1 peat bog in Marcell Experimental Forest and the Zim bog (Minnesota, USA). Total dissolved inorganic nitrogen (NO3-+NO2-+NH4+) and phosphate were both consistently < 2 μM in the porewater of surface peat, indicating severe nutrient limitation. While dissolved Fe was fairly abundant (18-35 mM), Mo, V and Cu were scarce (2-40 nM), suggesting that alternative metalloenzymes containing Fe in place of other metals may be favored. Rates of diazotrophy measured by both 15N2 incorporation and the acetylene (C2H2) reduction assay (ARA) were 7-fold higher under anoxic vs. oxic incubations conducted at both 4°C and 25°C. No significant difference in N2 fixation rates measured by either method was observed with or without the amendment of 1% CH4 at 25 °C; however, a significant inhibitory effect by methane was seen at 4°C in material from the S1 bog hollows. Anoxic 15N2 incorporation was 3-4x higher in treatments lacking acetylene, suggesting that the ARA likely underestimates N2 fixation by inhibiting diazotrophs sensitive to C2H2. Aerobic methanotrophy was also inhibited by 1% C2H2 when incubated under oxic conditions. No observations for the production of ethane (C2H6) were detected during the ARA, a biomarker for alternative nitrogenase activity. Major differences in ARA rates were observed to vary locally within microhabitats and between two bogs. In June 2014, peat sampled from hollows incubated under anoxic conditions showed the highest ARA rates (94.9 ± 11.0 nmol C2H4 g-1 moss dry mass hr-1), while the lowest rates were observed in
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hummock samples incubated under oxic conditions (5.1 ± 0.8 nmol C2H4 g-1 moss dry mass hr-1) in the S1 bog (T3 site). Observed rates have the potential to be a function of oxygen concentrations and or water content. ARA rates in all microcosm treatments were significantly lower at Zim bog compared to the S1 bog. The developed conversion factor between the regression of 15N2 and ARA in this study was 3.9 and agrees with the theoretical conversion factor as well as previous studies of soils and forest mosses.
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QUANTIFYING PEATLAND CARBON DYNAMICS USING MECHANISTICALLY-BASED BIOGEOCHEMISTRY MODELSSirui Wang (6623972) 11 June 2019 (has links)
<p></p><p></p><p>Peatlands are the most efficient natural carbon sink on the planet. They are the most carbon-intensive storages than any other vegetation types. However, recent studies indicate that global peatlands can potentially release 6% of the global soil carbon into the atmosphere when they are drained or deforested. They cover only about 3% of the total global land area, but sequester over 30% of the Earth’s soil organic carbon. Peatlands in northern mid-to-high latitudes (45°-90°N) occupy ~90% of the global peatland area and account for ~80% of the total global peat organic carbon stock. Those peatlands are mainly located in Canada, Russia, and the USA. Peatlands in tropical regions cover ~10% of the global peatlands area and store 15-19% of the global peat organic carbon. They are mainly distributed in Southeast Asia and South and Central America. The temperature at the global scale has been rising since the middle of the last century and has accelerated during the last 40 years and the warming will continue in this century. The large storage of soil organic carbon within the peatlands can significantly respond to the changing climate by varying the roles between their carbon sink (from atmosphere to soil) and source (from soil to atmosphere) activities. This dissertation focuses on quantifying the soil organic carbon dynamics in North America and South America using mechanistically-based biogeochemistry models. </p><p></p><p>Peatlands in Alaska occupy 40 million hectares and account for ~10% of the total peatland area in northern mid-to-high latitudes. The regional soil organic carbon dynamics and its response to climate are still with large uncertainty. Most of the studies on peatlands to date are based on short-term site-level observation. This dissertation first used an integrated modeling framework that coupled the dynamics of hydrology, soil thermal regime, and ecosystem carbon and nitrogen to quantify the long-term peat carbon accumulation in Alaska during the Holocene. Modeled hydrology, soil thermal regime, carbon pools and fluxes and methane emissions were evaluated using long-term observation data at several peatland sites in Minnesota, Alaska, and Canada. The model was then applied for a 10,000-year (15 ka to 5 ka; 1 ka = 1000 cal yr before present) simulation at four peatland sites. The model simulations matched the observed carbon accumulation rates at fen sites during the Holocene (R^2= 0.88, 0.87, 0.38 and -0.05 for four sites respectively using comparisons in 500-year bins from 15 ka to 5 ka). The simulated (2.04 m) and observed peat depths (on average 1.98 m) also compared well (R^2 = 0.91). The early Holocene carbon accumulation rates, especially during the Holocene thermal maximum (HTM) (35.9 g 〖C m〗^(-2) yr^(-1)), were estimated up to 6-times higher than the rest of the Holocene (6.5 g 〖C m〗^(-2) yr^(-1)). It suggested that high summer temperature and the lengthened growing season resulted from the elevated insolation seasonality, along with wetter-than-before conditions might be major factors causing the rapid carbon accumulation in Alaska during the HTM. The sensitivity tests indicated that, apart from climate, initial water-table depth and vegetation canopy were major drivers to the estimated peat carbon accumulation. </p><p></p><p>To further quantify the regional long-term soil organic carbon accumulation rates and the current carbon stocks in Alaska, the second part of my research focused on quantifying the soil organic carbon accumulation in multiple Alaskan terrestrial ecosystems over the last 15,000 years for both peatland and non-peatland ecosystems. Comparable with the previous estimates of 25-70 Pg carbon (C) in peatlands and 13-22 Pg C in non-peatland soils within 1-m depth in Alaska using peat core data, our model estimated a total SOC of 36-63 Pg C at present, including 27-48 Pg C in peatland soils and 9-15 Pg C in non-peatland soils. Current living vegetation stored 2.5-3.7 Pg C in Alaska with 0.3-0.6 Pg C in peatlands and 2.2-3.1 Pg C in non-peatlands. The simulated average rate of peat soil C accumulation was 2.3 Tg C yr^(-1) with a peak value of 5.1 Tg C yr^(-1) during the Holocene Thermal Maximum (HTM) in the early Holocene, four folds higher than the average rate of 1.4 Tg C yr^(-1) over the rest of the Holocene. The accumulation slowed down, or even ceased, during the neo-glacial climate cooling after the mid-Holocene, but increased again in the 20th century. The model-estimated peat depths ranged from 1.1 to 2.7 m, similar to the field-based estimate of 2.29 m for the region. The changes in vegetation and their distributions were the main factors to determine the spatial variations of SOC accumulation during different time periods. Warmer summer temperature and stronger radiation seasonality, along with higher precipitation in the HTM and the 20th century might have resulted in the extensive peatland expansion and carbon accumulation. </p><p>Most studies on the role of tropical peatlands have focused on Indonesian peatlands. Few have focused on the Amazon basin, where peatlands remain intact and have been a long-term carbon sink. To address the problem, my third study quantified the carbon accumulation for peatland and non-peatland ecosystems in the Pastaza-Marañon foreland basin (PMFB), the most extensive peatland complex in the Amazon basin from 12,000 years before present to 2100 AD. Model simulations indicated that warming accelerated peat carbon loss while increasing precipitation accelerated peat carbon accumulation at millennial time scales. The uncertain parameters and spatial variation of climate were significant sources of uncertainty to modeled peat carbon accumulation. Under warmer and presumably wetter conditions over the 21st century, the warming effect on increasing peat carbon loss might overwhelm the wetter effect on increasing peat carbon accumulation. Peat soil carbon accumulation rate in the PMFB slowed down to 7.9 (4.3~12.2) g C m^(-2) yr^(-1) from the current rate of 16.1 (9.1~23.7) g C m^(-2) yr^(-1) and the region might turn into a carbon source to the atmosphere at -53.3 (-66.8~-41.2) g C m^(-2) yr^(-1) (negative indicates source), depending on the level of warming. Peatland ecosystems showed a higher vulnerability than non-peatland ecosystems as indicated by the ratio of their soil carbon density changes (change of soil carbon/existing soil carbon stock) ranging from 3.9 to 5.8). This was primarily due to larger peatlands carbon stocks and more dramatic responses of their aerobic and anaerobic decompositions in comparison with non-peatland ecosystems under future climate conditions. Peatland and non-peatland soils in the PMFB might lose up to 0.4 (0.32~0.52) Pg C by 2100 AD with the largest loss from palm swamp. The carbon-dense Amazonian peatland might switch from a current carbon sink into a source in the 21st century.</p><p>Peatlands are important sources and sinks for greenhouse gases (carbon dioxide and methane). Their carbon (C) balance between soil and atmosphere remains unquantified due to the large data gaps and uncertainties in regional peat carbon estimation. My final study was to quantify the C accumulation rates and C stocks within North America peatlands over the last 12,000 years. I find that 85-174 Pg C have been accumulated in North American peatlands over these years including 0.37-0.76 Pg C in subtropical peatlands in this region. During the 10- 8 ka period, the warmer and wetter conditions might have played an important role in stimulating peat C accumulation by enhancing plant photosynthesis. The enhanced peat decomposition due to warming through the Holocene slows down carbon accumulation in the region.</p><div><br></div><p><br></p>
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