Wetland microtopography alters response of potential net CO
Coastal wetlands store significant amounts of carbon (C) belowground, which may be altered through effects of rising temperature and changing hydrology on CO2 and CH4 fluxes and related microbial activities. Wetland microtopography (hummock-hollow) also plays a critical role in mediating plant growt...
Ausführliche Beschreibung
Autor*in: |
Minick, Kevan J. [verfasserIn] Mitra, Bhaskar [verfasserIn] Li, Xuefeng [verfasserIn] Fischer, Milan [verfasserIn] Aguilos, Maricar [verfasserIn] Prajapati, Prajaya [verfasserIn] Noormets, Asko [verfasserIn] King, John S. [verfasserIn] |
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Format: |
E-Artikel |
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Sprache: |
Englisch |
Erschienen: |
2021 |
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Schlagwörter: |
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Übergeordnetes Werk: |
Enthalten in: Geoderma - Amsterdam [u.a.] : Elsevier Science, 1967, 402 |
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Übergeordnetes Werk: |
volume:402 |
DOI / URN: |
10.1016/j.geoderma.2021.115367 |
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Katalog-ID: |
ELV006497993 |
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520 | |a Coastal wetlands store significant amounts of carbon (C) belowground, which may be altered through effects of rising temperature and changing hydrology on CO2 and CH4 fluxes and related microbial activities. Wetland microtopography (hummock-hollow) also plays a critical role in mediating plant growth, microbial activity, and thus cycling of C and nutrients and may interact with rising seas to influence coastal wetland C dynamics. Recent evidence suggests that CH4 production in oxygenated surface soils of freshwater wetlands may contribute substantially to global CH4 production, but comprehensive studies linking potential CH4 production to environmental and microbial variables in temperate freshwater forested wetlands are lacking. This study investigated effects of temperature, moisture, and microtopography on potential net CO2 and CH4 production and extracellular enzyme activity (β-glucosidase, xylosidase, phenol oxidase, and peroxidase) in peat soils collected from a freshwater forested wetland in coastal North Carolina, USA. Soils were retrieved from three microsites (hummock, hollow, and subsurface peat soils (approximately 20–40 cm below surface)) and incubated at two temperatures (27 °C and 32 °C) and soil water contents (65% and 100% water holding capacity (WHC)). Hummocks had the highest cumulative potential net CO2 (13.7 ± 0.90 mg CO2-C g soil−1) and CH4 (1.8 ± 0.42 mg CH4-C g soil−1) production and enzyme activity, followed by hollows (8.7 ± 0.91 mg CO2-C g soil−1 and 0.5 ± 0.12 mg CH4-C g soil−1) and then subsurface soils (5.7 ± 0.70 mg CO2-C g soil−1 and 0.04 ± 0.019 mg CH4-C g soil−1). Fully saturated soils had lower potential net CO2 production (50–80%) and substantially higher potential net CH4 production compared to non-saturated soils (those incubated at 65% WHC). Soils incubated at 32 °C increased potential net CO2 (24–34%) and CH4 (56–404%) production under both soil moisture levels compared to those incubated at 27 °C. The Q10 values for potential net CO2 and CH4 production ranged from 1.5 to 2.3 and 3.3–8.8, respectively, and did not differ between any microsites or soil water content. Enrichment of δ13CO2-C was found in saturated soils from all microsites (−24.4 to − 29.7 ‰) compared to non-saturated soils (−31.1 to − 32.4 ‰), while δ13CH4-C ranged from −62 to −55‰ in saturated soils. Together, the CO2 and CH4 δ13C data suggest that acetoclastic methanogenesis is an important pathway for CH4 production in these wetlands. A positive relationship (Adj. R2 = 0.40) between peroxidase activity and CH4 production was also found, indicating that peroxidase activity may be important in providing fermented C substrates to acetoclastic methanogenic communities and contribute to anaerobic C mineralization. These results suggest that changes in temperature and hydrology could stimulate CO2 and CH4 emissions from surface hummock soils, and to a lesser extent from hollow soils, and provide preliminary evidence that hummocks may be a spatially important and unrecognized hotspot for CH4 production. | ||
650 | 4 | |a Methanogenesis | |
650 | 4 | |a Anaerobic respiration | |
650 | 4 | |a Peat | |
650 | 4 | |a Stable carbon isotopes | |
650 | 4 | |a Extracellular enzyme activity | |
650 | 4 | |a forested wetland | |
700 | 1 | |a Mitra, Bhaskar |e verfasserin |4 aut | |
700 | 1 | |a Li, Xuefeng |e verfasserin |4 aut | |
700 | 1 | |a Fischer, Milan |e verfasserin |4 aut | |
700 | 1 | |a Aguilos, Maricar |e verfasserin |0 (orcid)0000-0002-1949-3736 |4 aut | |
700 | 1 | |a Prajapati, Prajaya |e verfasserin |4 aut | |
700 | 1 | |a Noormets, Asko |e verfasserin |4 aut | |
700 | 1 | |a King, John S. |e verfasserin |0 (orcid)0000-0002-9345-9800 |4 aut | |
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10.1016/j.geoderma.2021.115367 doi (DE-627)ELV006497993 (ELSEVIER)S0016-7061(21)00447-X DE-627 ger DE-627 rda eng 550 910 DE-600 38.60 bkl Minick, Kevan J. verfasserin aut Wetland microtopography alters response of potential net CO 2021 nicht spezifiziert zzz rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier Coastal wetlands store significant amounts of carbon (C) belowground, which may be altered through effects of rising temperature and changing hydrology on CO2 and CH4 fluxes and related microbial activities. Wetland microtopography (hummock-hollow) also plays a critical role in mediating plant growth, microbial activity, and thus cycling of C and nutrients and may interact with rising seas to influence coastal wetland C dynamics. Recent evidence suggests that CH4 production in oxygenated surface soils of freshwater wetlands may contribute substantially to global CH4 production, but comprehensive studies linking potential CH4 production to environmental and microbial variables in temperate freshwater forested wetlands are lacking. This study investigated effects of temperature, moisture, and microtopography on potential net CO2 and CH4 production and extracellular enzyme activity (β-glucosidase, xylosidase, phenol oxidase, and peroxidase) in peat soils collected from a freshwater forested wetland in coastal North Carolina, USA. Soils were retrieved from three microsites (hummock, hollow, and subsurface peat soils (approximately 20–40 cm below surface)) and incubated at two temperatures (27 °C and 32 °C) and soil water contents (65% and 100% water holding capacity (WHC)). Hummocks had the highest cumulative potential net CO2 (13.7 ± 0.90 mg CO2-C g soil−1) and CH4 (1.8 ± 0.42 mg CH4-C g soil−1) production and enzyme activity, followed by hollows (8.7 ± 0.91 mg CO2-C g soil−1 and 0.5 ± 0.12 mg CH4-C g soil−1) and then subsurface soils (5.7 ± 0.70 mg CO2-C g soil−1 and 0.04 ± 0.019 mg CH4-C g soil−1). Fully saturated soils had lower potential net CO2 production (50–80%) and substantially higher potential net CH4 production compared to non-saturated soils (those incubated at 65% WHC). Soils incubated at 32 °C increased potential net CO2 (24–34%) and CH4 (56–404%) production under both soil moisture levels compared to those incubated at 27 °C. The Q10 values for potential net CO2 and CH4 production ranged from 1.5 to 2.3 and 3.3–8.8, respectively, and did not differ between any microsites or soil water content. Enrichment of δ13CO2-C was found in saturated soils from all microsites (−24.4 to − 29.7 ‰) compared to non-saturated soils (−31.1 to − 32.4 ‰), while δ13CH4-C ranged from −62 to −55‰ in saturated soils. Together, the CO2 and CH4 δ13C data suggest that acetoclastic methanogenesis is an important pathway for CH4 production in these wetlands. A positive relationship (Adj. R2 = 0.40) between peroxidase activity and CH4 production was also found, indicating that peroxidase activity may be important in providing fermented C substrates to acetoclastic methanogenic communities and contribute to anaerobic C mineralization. These results suggest that changes in temperature and hydrology could stimulate CO2 and CH4 emissions from surface hummock soils, and to a lesser extent from hollow soils, and provide preliminary evidence that hummocks may be a spatially important and unrecognized hotspot for CH4 production. Methanogenesis Anaerobic respiration Peat Stable carbon isotopes Extracellular enzyme activity forested wetland Mitra, Bhaskar verfasserin aut Li, Xuefeng verfasserin aut Fischer, Milan verfasserin aut Aguilos, Maricar verfasserin (orcid)0000-0002-1949-3736 aut Prajapati, Prajaya verfasserin aut Noormets, Asko verfasserin aut King, John S. verfasserin (orcid)0000-0002-9345-9800 aut Enthalten in Geoderma Amsterdam [u.a.] : Elsevier Science, 1967 402 Online-Ressource (DE-627)320414493 (DE-600)2001729-7 (DE-576)099603853 1872-6259 nnns volume:402 GBV_USEFLAG_U SYSFLAG_U GBV_ELV SSG-OPC-GGO GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_24 GBV_ILN_31 GBV_ILN_32 GBV_ILN_40 GBV_ILN_60 GBV_ILN_62 GBV_ILN_63 GBV_ILN_65 GBV_ILN_69 GBV_ILN_70 GBV_ILN_73 GBV_ILN_74 GBV_ILN_90 GBV_ILN_95 GBV_ILN_100 GBV_ILN_105 GBV_ILN_110 GBV_ILN_150 GBV_ILN_151 GBV_ILN_187 GBV_ILN_213 GBV_ILN_224 GBV_ILN_230 GBV_ILN_370 GBV_ILN_602 GBV_ILN_702 GBV_ILN_2003 GBV_ILN_2004 GBV_ILN_2005 GBV_ILN_2007 GBV_ILN_2009 GBV_ILN_2011 GBV_ILN_2014 GBV_ILN_2015 GBV_ILN_2020 GBV_ILN_2021 GBV_ILN_2025 GBV_ILN_2027 GBV_ILN_2034 GBV_ILN_2038 GBV_ILN_2044 GBV_ILN_2048 GBV_ILN_2049 GBV_ILN_2050 GBV_ILN_2055 GBV_ILN_2056 GBV_ILN_2059 GBV_ILN_2061 GBV_ILN_2064 GBV_ILN_2065 GBV_ILN_2068 GBV_ILN_2106 GBV_ILN_2111 GBV_ILN_2112 GBV_ILN_2113 GBV_ILN_2118 GBV_ILN_2122 GBV_ILN_2129 GBV_ILN_2143 GBV_ILN_2147 GBV_ILN_2148 GBV_ILN_2152 GBV_ILN_2153 GBV_ILN_2190 GBV_ILN_2232 GBV_ILN_2336 GBV_ILN_2470 GBV_ILN_2507 GBV_ILN_2522 GBV_ILN_4035 GBV_ILN_4037 GBV_ILN_4112 GBV_ILN_4125 GBV_ILN_4126 GBV_ILN_4242 GBV_ILN_4251 GBV_ILN_4305 GBV_ILN_4313 GBV_ILN_4322 GBV_ILN_4323 GBV_ILN_4324 GBV_ILN_4326 GBV_ILN_4333 GBV_ILN_4334 GBV_ILN_4335 GBV_ILN_4338 GBV_ILN_4393 GBV_ILN_4700 38.60 Bodenkunde: Allgemeines Geowissenschaften AR 402 |
spelling |
10.1016/j.geoderma.2021.115367 doi (DE-627)ELV006497993 (ELSEVIER)S0016-7061(21)00447-X DE-627 ger DE-627 rda eng 550 910 DE-600 38.60 bkl Minick, Kevan J. verfasserin aut Wetland microtopography alters response of potential net CO 2021 nicht spezifiziert zzz rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier Coastal wetlands store significant amounts of carbon (C) belowground, which may be altered through effects of rising temperature and changing hydrology on CO2 and CH4 fluxes and related microbial activities. Wetland microtopography (hummock-hollow) also plays a critical role in mediating plant growth, microbial activity, and thus cycling of C and nutrients and may interact with rising seas to influence coastal wetland C dynamics. Recent evidence suggests that CH4 production in oxygenated surface soils of freshwater wetlands may contribute substantially to global CH4 production, but comprehensive studies linking potential CH4 production to environmental and microbial variables in temperate freshwater forested wetlands are lacking. This study investigated effects of temperature, moisture, and microtopography on potential net CO2 and CH4 production and extracellular enzyme activity (β-glucosidase, xylosidase, phenol oxidase, and peroxidase) in peat soils collected from a freshwater forested wetland in coastal North Carolina, USA. Soils were retrieved from three microsites (hummock, hollow, and subsurface peat soils (approximately 20–40 cm below surface)) and incubated at two temperatures (27 °C and 32 °C) and soil water contents (65% and 100% water holding capacity (WHC)). Hummocks had the highest cumulative potential net CO2 (13.7 ± 0.90 mg CO2-C g soil−1) and CH4 (1.8 ± 0.42 mg CH4-C g soil−1) production and enzyme activity, followed by hollows (8.7 ± 0.91 mg CO2-C g soil−1 and 0.5 ± 0.12 mg CH4-C g soil−1) and then subsurface soils (5.7 ± 0.70 mg CO2-C g soil−1 and 0.04 ± 0.019 mg CH4-C g soil−1). Fully saturated soils had lower potential net CO2 production (50–80%) and substantially higher potential net CH4 production compared to non-saturated soils (those incubated at 65% WHC). Soils incubated at 32 °C increased potential net CO2 (24–34%) and CH4 (56–404%) production under both soil moisture levels compared to those incubated at 27 °C. The Q10 values for potential net CO2 and CH4 production ranged from 1.5 to 2.3 and 3.3–8.8, respectively, and did not differ between any microsites or soil water content. Enrichment of δ13CO2-C was found in saturated soils from all microsites (−24.4 to − 29.7 ‰) compared to non-saturated soils (−31.1 to − 32.4 ‰), while δ13CH4-C ranged from −62 to −55‰ in saturated soils. Together, the CO2 and CH4 δ13C data suggest that acetoclastic methanogenesis is an important pathway for CH4 production in these wetlands. A positive relationship (Adj. R2 = 0.40) between peroxidase activity and CH4 production was also found, indicating that peroxidase activity may be important in providing fermented C substrates to acetoclastic methanogenic communities and contribute to anaerobic C mineralization. These results suggest that changes in temperature and hydrology could stimulate CO2 and CH4 emissions from surface hummock soils, and to a lesser extent from hollow soils, and provide preliminary evidence that hummocks may be a spatially important and unrecognized hotspot for CH4 production. Methanogenesis Anaerobic respiration Peat Stable carbon isotopes Extracellular enzyme activity forested wetland Mitra, Bhaskar verfasserin aut Li, Xuefeng verfasserin aut Fischer, Milan verfasserin aut Aguilos, Maricar verfasserin (orcid)0000-0002-1949-3736 aut Prajapati, Prajaya verfasserin aut Noormets, Asko verfasserin aut King, John S. verfasserin (orcid)0000-0002-9345-9800 aut Enthalten in Geoderma Amsterdam [u.a.] : Elsevier Science, 1967 402 Online-Ressource (DE-627)320414493 (DE-600)2001729-7 (DE-576)099603853 1872-6259 nnns volume:402 GBV_USEFLAG_U SYSFLAG_U GBV_ELV SSG-OPC-GGO GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_24 GBV_ILN_31 GBV_ILN_32 GBV_ILN_40 GBV_ILN_60 GBV_ILN_62 GBV_ILN_63 GBV_ILN_65 GBV_ILN_69 GBV_ILN_70 GBV_ILN_73 GBV_ILN_74 GBV_ILN_90 GBV_ILN_95 GBV_ILN_100 GBV_ILN_105 GBV_ILN_110 GBV_ILN_150 GBV_ILN_151 GBV_ILN_187 GBV_ILN_213 GBV_ILN_224 GBV_ILN_230 GBV_ILN_370 GBV_ILN_602 GBV_ILN_702 GBV_ILN_2003 GBV_ILN_2004 GBV_ILN_2005 GBV_ILN_2007 GBV_ILN_2009 GBV_ILN_2011 GBV_ILN_2014 GBV_ILN_2015 GBV_ILN_2020 GBV_ILN_2021 GBV_ILN_2025 GBV_ILN_2027 GBV_ILN_2034 GBV_ILN_2038 GBV_ILN_2044 GBV_ILN_2048 GBV_ILN_2049 GBV_ILN_2050 GBV_ILN_2055 GBV_ILN_2056 GBV_ILN_2059 GBV_ILN_2061 GBV_ILN_2064 GBV_ILN_2065 GBV_ILN_2068 GBV_ILN_2106 GBV_ILN_2111 GBV_ILN_2112 GBV_ILN_2113 GBV_ILN_2118 GBV_ILN_2122 GBV_ILN_2129 GBV_ILN_2143 GBV_ILN_2147 GBV_ILN_2148 GBV_ILN_2152 GBV_ILN_2153 GBV_ILN_2190 GBV_ILN_2232 GBV_ILN_2336 GBV_ILN_2470 GBV_ILN_2507 GBV_ILN_2522 GBV_ILN_4035 GBV_ILN_4037 GBV_ILN_4112 GBV_ILN_4125 GBV_ILN_4126 GBV_ILN_4242 GBV_ILN_4251 GBV_ILN_4305 GBV_ILN_4313 GBV_ILN_4322 GBV_ILN_4323 GBV_ILN_4324 GBV_ILN_4326 GBV_ILN_4333 GBV_ILN_4334 GBV_ILN_4335 GBV_ILN_4338 GBV_ILN_4393 GBV_ILN_4700 38.60 Bodenkunde: Allgemeines Geowissenschaften AR 402 |
allfields_unstemmed |
10.1016/j.geoderma.2021.115367 doi (DE-627)ELV006497993 (ELSEVIER)S0016-7061(21)00447-X DE-627 ger DE-627 rda eng 550 910 DE-600 38.60 bkl Minick, Kevan J. verfasserin aut Wetland microtopography alters response of potential net CO 2021 nicht spezifiziert zzz rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier Coastal wetlands store significant amounts of carbon (C) belowground, which may be altered through effects of rising temperature and changing hydrology on CO2 and CH4 fluxes and related microbial activities. Wetland microtopography (hummock-hollow) also plays a critical role in mediating plant growth, microbial activity, and thus cycling of C and nutrients and may interact with rising seas to influence coastal wetland C dynamics. Recent evidence suggests that CH4 production in oxygenated surface soils of freshwater wetlands may contribute substantially to global CH4 production, but comprehensive studies linking potential CH4 production to environmental and microbial variables in temperate freshwater forested wetlands are lacking. This study investigated effects of temperature, moisture, and microtopography on potential net CO2 and CH4 production and extracellular enzyme activity (β-glucosidase, xylosidase, phenol oxidase, and peroxidase) in peat soils collected from a freshwater forested wetland in coastal North Carolina, USA. Soils were retrieved from three microsites (hummock, hollow, and subsurface peat soils (approximately 20–40 cm below surface)) and incubated at two temperatures (27 °C and 32 °C) and soil water contents (65% and 100% water holding capacity (WHC)). Hummocks had the highest cumulative potential net CO2 (13.7 ± 0.90 mg CO2-C g soil−1) and CH4 (1.8 ± 0.42 mg CH4-C g soil−1) production and enzyme activity, followed by hollows (8.7 ± 0.91 mg CO2-C g soil−1 and 0.5 ± 0.12 mg CH4-C g soil−1) and then subsurface soils (5.7 ± 0.70 mg CO2-C g soil−1 and 0.04 ± 0.019 mg CH4-C g soil−1). Fully saturated soils had lower potential net CO2 production (50–80%) and substantially higher potential net CH4 production compared to non-saturated soils (those incubated at 65% WHC). Soils incubated at 32 °C increased potential net CO2 (24–34%) and CH4 (56–404%) production under both soil moisture levels compared to those incubated at 27 °C. The Q10 values for potential net CO2 and CH4 production ranged from 1.5 to 2.3 and 3.3–8.8, respectively, and did not differ between any microsites or soil water content. Enrichment of δ13CO2-C was found in saturated soils from all microsites (−24.4 to − 29.7 ‰) compared to non-saturated soils (−31.1 to − 32.4 ‰), while δ13CH4-C ranged from −62 to −55‰ in saturated soils. Together, the CO2 and CH4 δ13C data suggest that acetoclastic methanogenesis is an important pathway for CH4 production in these wetlands. A positive relationship (Adj. R2 = 0.40) between peroxidase activity and CH4 production was also found, indicating that peroxidase activity may be important in providing fermented C substrates to acetoclastic methanogenic communities and contribute to anaerobic C mineralization. These results suggest that changes in temperature and hydrology could stimulate CO2 and CH4 emissions from surface hummock soils, and to a lesser extent from hollow soils, and provide preliminary evidence that hummocks may be a spatially important and unrecognized hotspot for CH4 production. Methanogenesis Anaerobic respiration Peat Stable carbon isotopes Extracellular enzyme activity forested wetland Mitra, Bhaskar verfasserin aut Li, Xuefeng verfasserin aut Fischer, Milan verfasserin aut Aguilos, Maricar verfasserin (orcid)0000-0002-1949-3736 aut Prajapati, Prajaya verfasserin aut Noormets, Asko verfasserin aut King, John S. verfasserin (orcid)0000-0002-9345-9800 aut Enthalten in Geoderma Amsterdam [u.a.] : Elsevier Science, 1967 402 Online-Ressource (DE-627)320414493 (DE-600)2001729-7 (DE-576)099603853 1872-6259 nnns volume:402 GBV_USEFLAG_U SYSFLAG_U GBV_ELV SSG-OPC-GGO GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_24 GBV_ILN_31 GBV_ILN_32 GBV_ILN_40 GBV_ILN_60 GBV_ILN_62 GBV_ILN_63 GBV_ILN_65 GBV_ILN_69 GBV_ILN_70 GBV_ILN_73 GBV_ILN_74 GBV_ILN_90 GBV_ILN_95 GBV_ILN_100 GBV_ILN_105 GBV_ILN_110 GBV_ILN_150 GBV_ILN_151 GBV_ILN_187 GBV_ILN_213 GBV_ILN_224 GBV_ILN_230 GBV_ILN_370 GBV_ILN_602 GBV_ILN_702 GBV_ILN_2003 GBV_ILN_2004 GBV_ILN_2005 GBV_ILN_2007 GBV_ILN_2009 GBV_ILN_2011 GBV_ILN_2014 GBV_ILN_2015 GBV_ILN_2020 GBV_ILN_2021 GBV_ILN_2025 GBV_ILN_2027 GBV_ILN_2034 GBV_ILN_2038 GBV_ILN_2044 GBV_ILN_2048 GBV_ILN_2049 GBV_ILN_2050 GBV_ILN_2055 GBV_ILN_2056 GBV_ILN_2059 GBV_ILN_2061 GBV_ILN_2064 GBV_ILN_2065 GBV_ILN_2068 GBV_ILN_2106 GBV_ILN_2111 GBV_ILN_2112 GBV_ILN_2113 GBV_ILN_2118 GBV_ILN_2122 GBV_ILN_2129 GBV_ILN_2143 GBV_ILN_2147 GBV_ILN_2148 GBV_ILN_2152 GBV_ILN_2153 GBV_ILN_2190 GBV_ILN_2232 GBV_ILN_2336 GBV_ILN_2470 GBV_ILN_2507 GBV_ILN_2522 GBV_ILN_4035 GBV_ILN_4037 GBV_ILN_4112 GBV_ILN_4125 GBV_ILN_4126 GBV_ILN_4242 GBV_ILN_4251 GBV_ILN_4305 GBV_ILN_4313 GBV_ILN_4322 GBV_ILN_4323 GBV_ILN_4324 GBV_ILN_4326 GBV_ILN_4333 GBV_ILN_4334 GBV_ILN_4335 GBV_ILN_4338 GBV_ILN_4393 GBV_ILN_4700 38.60 Bodenkunde: Allgemeines Geowissenschaften AR 402 |
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10.1016/j.geoderma.2021.115367 doi (DE-627)ELV006497993 (ELSEVIER)S0016-7061(21)00447-X DE-627 ger DE-627 rda eng 550 910 DE-600 38.60 bkl Minick, Kevan J. verfasserin aut Wetland microtopography alters response of potential net CO 2021 nicht spezifiziert zzz rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier Coastal wetlands store significant amounts of carbon (C) belowground, which may be altered through effects of rising temperature and changing hydrology on CO2 and CH4 fluxes and related microbial activities. Wetland microtopography (hummock-hollow) also plays a critical role in mediating plant growth, microbial activity, and thus cycling of C and nutrients and may interact with rising seas to influence coastal wetland C dynamics. Recent evidence suggests that CH4 production in oxygenated surface soils of freshwater wetlands may contribute substantially to global CH4 production, but comprehensive studies linking potential CH4 production to environmental and microbial variables in temperate freshwater forested wetlands are lacking. This study investigated effects of temperature, moisture, and microtopography on potential net CO2 and CH4 production and extracellular enzyme activity (β-glucosidase, xylosidase, phenol oxidase, and peroxidase) in peat soils collected from a freshwater forested wetland in coastal North Carolina, USA. Soils were retrieved from three microsites (hummock, hollow, and subsurface peat soils (approximately 20–40 cm below surface)) and incubated at two temperatures (27 °C and 32 °C) and soil water contents (65% and 100% water holding capacity (WHC)). Hummocks had the highest cumulative potential net CO2 (13.7 ± 0.90 mg CO2-C g soil−1) and CH4 (1.8 ± 0.42 mg CH4-C g soil−1) production and enzyme activity, followed by hollows (8.7 ± 0.91 mg CO2-C g soil−1 and 0.5 ± 0.12 mg CH4-C g soil−1) and then subsurface soils (5.7 ± 0.70 mg CO2-C g soil−1 and 0.04 ± 0.019 mg CH4-C g soil−1). Fully saturated soils had lower potential net CO2 production (50–80%) and substantially higher potential net CH4 production compared to non-saturated soils (those incubated at 65% WHC). Soils incubated at 32 °C increased potential net CO2 (24–34%) and CH4 (56–404%) production under both soil moisture levels compared to those incubated at 27 °C. The Q10 values for potential net CO2 and CH4 production ranged from 1.5 to 2.3 and 3.3–8.8, respectively, and did not differ between any microsites or soil water content. Enrichment of δ13CO2-C was found in saturated soils from all microsites (−24.4 to − 29.7 ‰) compared to non-saturated soils (−31.1 to − 32.4 ‰), while δ13CH4-C ranged from −62 to −55‰ in saturated soils. Together, the CO2 and CH4 δ13C data suggest that acetoclastic methanogenesis is an important pathway for CH4 production in these wetlands. A positive relationship (Adj. R2 = 0.40) between peroxidase activity and CH4 production was also found, indicating that peroxidase activity may be important in providing fermented C substrates to acetoclastic methanogenic communities and contribute to anaerobic C mineralization. These results suggest that changes in temperature and hydrology could stimulate CO2 and CH4 emissions from surface hummock soils, and to a lesser extent from hollow soils, and provide preliminary evidence that hummocks may be a spatially important and unrecognized hotspot for CH4 production. Methanogenesis Anaerobic respiration Peat Stable carbon isotopes Extracellular enzyme activity forested wetland Mitra, Bhaskar verfasserin aut Li, Xuefeng verfasserin aut Fischer, Milan verfasserin aut Aguilos, Maricar verfasserin (orcid)0000-0002-1949-3736 aut Prajapati, Prajaya verfasserin aut Noormets, Asko verfasserin aut King, John S. verfasserin (orcid)0000-0002-9345-9800 aut Enthalten in Geoderma Amsterdam [u.a.] : Elsevier Science, 1967 402 Online-Ressource (DE-627)320414493 (DE-600)2001729-7 (DE-576)099603853 1872-6259 nnns volume:402 GBV_USEFLAG_U SYSFLAG_U GBV_ELV SSG-OPC-GGO GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_24 GBV_ILN_31 GBV_ILN_32 GBV_ILN_40 GBV_ILN_60 GBV_ILN_62 GBV_ILN_63 GBV_ILN_65 GBV_ILN_69 GBV_ILN_70 GBV_ILN_73 GBV_ILN_74 GBV_ILN_90 GBV_ILN_95 GBV_ILN_100 GBV_ILN_105 GBV_ILN_110 GBV_ILN_150 GBV_ILN_151 GBV_ILN_187 GBV_ILN_213 GBV_ILN_224 GBV_ILN_230 GBV_ILN_370 GBV_ILN_602 GBV_ILN_702 GBV_ILN_2003 GBV_ILN_2004 GBV_ILN_2005 GBV_ILN_2007 GBV_ILN_2009 GBV_ILN_2011 GBV_ILN_2014 GBV_ILN_2015 GBV_ILN_2020 GBV_ILN_2021 GBV_ILN_2025 GBV_ILN_2027 GBV_ILN_2034 GBV_ILN_2038 GBV_ILN_2044 GBV_ILN_2048 GBV_ILN_2049 GBV_ILN_2050 GBV_ILN_2055 GBV_ILN_2056 GBV_ILN_2059 GBV_ILN_2061 GBV_ILN_2064 GBV_ILN_2065 GBV_ILN_2068 GBV_ILN_2106 GBV_ILN_2111 GBV_ILN_2112 GBV_ILN_2113 GBV_ILN_2118 GBV_ILN_2122 GBV_ILN_2129 GBV_ILN_2143 GBV_ILN_2147 GBV_ILN_2148 GBV_ILN_2152 GBV_ILN_2153 GBV_ILN_2190 GBV_ILN_2232 GBV_ILN_2336 GBV_ILN_2470 GBV_ILN_2507 GBV_ILN_2522 GBV_ILN_4035 GBV_ILN_4037 GBV_ILN_4112 GBV_ILN_4125 GBV_ILN_4126 GBV_ILN_4242 GBV_ILN_4251 GBV_ILN_4305 GBV_ILN_4313 GBV_ILN_4322 GBV_ILN_4323 GBV_ILN_4324 GBV_ILN_4326 GBV_ILN_4333 GBV_ILN_4334 GBV_ILN_4335 GBV_ILN_4338 GBV_ILN_4393 GBV_ILN_4700 38.60 Bodenkunde: Allgemeines Geowissenschaften AR 402 |
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10.1016/j.geoderma.2021.115367 doi (DE-627)ELV006497993 (ELSEVIER)S0016-7061(21)00447-X DE-627 ger DE-627 rda eng 550 910 DE-600 38.60 bkl Minick, Kevan J. verfasserin aut Wetland microtopography alters response of potential net CO 2021 nicht spezifiziert zzz rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier Coastal wetlands store significant amounts of carbon (C) belowground, which may be altered through effects of rising temperature and changing hydrology on CO2 and CH4 fluxes and related microbial activities. Wetland microtopography (hummock-hollow) also plays a critical role in mediating plant growth, microbial activity, and thus cycling of C and nutrients and may interact with rising seas to influence coastal wetland C dynamics. Recent evidence suggests that CH4 production in oxygenated surface soils of freshwater wetlands may contribute substantially to global CH4 production, but comprehensive studies linking potential CH4 production to environmental and microbial variables in temperate freshwater forested wetlands are lacking. This study investigated effects of temperature, moisture, and microtopography on potential net CO2 and CH4 production and extracellular enzyme activity (β-glucosidase, xylosidase, phenol oxidase, and peroxidase) in peat soils collected from a freshwater forested wetland in coastal North Carolina, USA. Soils were retrieved from three microsites (hummock, hollow, and subsurface peat soils (approximately 20–40 cm below surface)) and incubated at two temperatures (27 °C and 32 °C) and soil water contents (65% and 100% water holding capacity (WHC)). Hummocks had the highest cumulative potential net CO2 (13.7 ± 0.90 mg CO2-C g soil−1) and CH4 (1.8 ± 0.42 mg CH4-C g soil−1) production and enzyme activity, followed by hollows (8.7 ± 0.91 mg CO2-C g soil−1 and 0.5 ± 0.12 mg CH4-C g soil−1) and then subsurface soils (5.7 ± 0.70 mg CO2-C g soil−1 and 0.04 ± 0.019 mg CH4-C g soil−1). Fully saturated soils had lower potential net CO2 production (50–80%) and substantially higher potential net CH4 production compared to non-saturated soils (those incubated at 65% WHC). Soils incubated at 32 °C increased potential net CO2 (24–34%) and CH4 (56–404%) production under both soil moisture levels compared to those incubated at 27 °C. The Q10 values for potential net CO2 and CH4 production ranged from 1.5 to 2.3 and 3.3–8.8, respectively, and did not differ between any microsites or soil water content. Enrichment of δ13CO2-C was found in saturated soils from all microsites (−24.4 to − 29.7 ‰) compared to non-saturated soils (−31.1 to − 32.4 ‰), while δ13CH4-C ranged from −62 to −55‰ in saturated soils. Together, the CO2 and CH4 δ13C data suggest that acetoclastic methanogenesis is an important pathway for CH4 production in these wetlands. A positive relationship (Adj. R2 = 0.40) between peroxidase activity and CH4 production was also found, indicating that peroxidase activity may be important in providing fermented C substrates to acetoclastic methanogenic communities and contribute to anaerobic C mineralization. These results suggest that changes in temperature and hydrology could stimulate CO2 and CH4 emissions from surface hummock soils, and to a lesser extent from hollow soils, and provide preliminary evidence that hummocks may be a spatially important and unrecognized hotspot for CH4 production. Methanogenesis Anaerobic respiration Peat Stable carbon isotopes Extracellular enzyme activity forested wetland Mitra, Bhaskar verfasserin aut Li, Xuefeng verfasserin aut Fischer, Milan verfasserin aut Aguilos, Maricar verfasserin (orcid)0000-0002-1949-3736 aut Prajapati, Prajaya verfasserin aut Noormets, Asko verfasserin aut King, John S. verfasserin (orcid)0000-0002-9345-9800 aut Enthalten in Geoderma Amsterdam [u.a.] : Elsevier Science, 1967 402 Online-Ressource (DE-627)320414493 (DE-600)2001729-7 (DE-576)099603853 1872-6259 nnns volume:402 GBV_USEFLAG_U SYSFLAG_U GBV_ELV SSG-OPC-GGO GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_24 GBV_ILN_31 GBV_ILN_32 GBV_ILN_40 GBV_ILN_60 GBV_ILN_62 GBV_ILN_63 GBV_ILN_65 GBV_ILN_69 GBV_ILN_70 GBV_ILN_73 GBV_ILN_74 GBV_ILN_90 GBV_ILN_95 GBV_ILN_100 GBV_ILN_105 GBV_ILN_110 GBV_ILN_150 GBV_ILN_151 GBV_ILN_187 GBV_ILN_213 GBV_ILN_224 GBV_ILN_230 GBV_ILN_370 GBV_ILN_602 GBV_ILN_702 GBV_ILN_2003 GBV_ILN_2004 GBV_ILN_2005 GBV_ILN_2007 GBV_ILN_2009 GBV_ILN_2011 GBV_ILN_2014 GBV_ILN_2015 GBV_ILN_2020 GBV_ILN_2021 GBV_ILN_2025 GBV_ILN_2027 GBV_ILN_2034 GBV_ILN_2038 GBV_ILN_2044 GBV_ILN_2048 GBV_ILN_2049 GBV_ILN_2050 GBV_ILN_2055 GBV_ILN_2056 GBV_ILN_2059 GBV_ILN_2061 GBV_ILN_2064 GBV_ILN_2065 GBV_ILN_2068 GBV_ILN_2106 GBV_ILN_2111 GBV_ILN_2112 GBV_ILN_2113 GBV_ILN_2118 GBV_ILN_2122 GBV_ILN_2129 GBV_ILN_2143 GBV_ILN_2147 GBV_ILN_2148 GBV_ILN_2152 GBV_ILN_2153 GBV_ILN_2190 GBV_ILN_2232 GBV_ILN_2336 GBV_ILN_2470 GBV_ILN_2507 GBV_ILN_2522 GBV_ILN_4035 GBV_ILN_4037 GBV_ILN_4112 GBV_ILN_4125 GBV_ILN_4126 GBV_ILN_4242 GBV_ILN_4251 GBV_ILN_4305 GBV_ILN_4313 GBV_ILN_4322 GBV_ILN_4323 GBV_ILN_4324 GBV_ILN_4326 GBV_ILN_4333 GBV_ILN_4334 GBV_ILN_4335 GBV_ILN_4338 GBV_ILN_4393 GBV_ILN_4700 38.60 Bodenkunde: Allgemeines Geowissenschaften AR 402 |
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Minick, Kevan J. @@aut@@ Mitra, Bhaskar @@aut@@ Li, Xuefeng @@aut@@ Fischer, Milan @@aut@@ Aguilos, Maricar @@aut@@ Prajapati, Prajaya @@aut@@ Noormets, Asko @@aut@@ King, John S. @@aut@@ |
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Soils were retrieved from three microsites (hummock, hollow, and subsurface peat soils (approximately 20–40 cm below surface)) and incubated at two temperatures (27 °C and 32 °C) and soil water contents (65% and 100% water holding capacity (WHC)). Hummocks had the highest cumulative potential net CO2 (13.7 ± 0.90 mg CO2-C g soil−1) and CH4 (1.8 ± 0.42 mg CH4-C g soil−1) production and enzyme activity, followed by hollows (8.7 ± 0.91 mg CO2-C g soil−1 and 0.5 ± 0.12 mg CH4-C g soil−1) and then subsurface soils (5.7 ± 0.70 mg CO2-C g soil−1 and 0.04 ± 0.019 mg CH4-C g soil−1). Fully saturated soils had lower potential net CO2 production (50–80%) and substantially higher potential net CH4 production compared to non-saturated soils (those incubated at 65% WHC). Soils incubated at 32 °C increased potential net CO2 (24–34%) and CH4 (56–404%) production under both soil moisture levels compared to those incubated at 27 °C. 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Wetland microtopography alters response of potential net CO |
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wetland microtopography alters response of potential net co |
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Wetland microtopography alters response of potential net CO |
abstract |
Coastal wetlands store significant amounts of carbon (C) belowground, which may be altered through effects of rising temperature and changing hydrology on CO2 and CH4 fluxes and related microbial activities. Wetland microtopography (hummock-hollow) also plays a critical role in mediating plant growth, microbial activity, and thus cycling of C and nutrients and may interact with rising seas to influence coastal wetland C dynamics. Recent evidence suggests that CH4 production in oxygenated surface soils of freshwater wetlands may contribute substantially to global CH4 production, but comprehensive studies linking potential CH4 production to environmental and microbial variables in temperate freshwater forested wetlands are lacking. This study investigated effects of temperature, moisture, and microtopography on potential net CO2 and CH4 production and extracellular enzyme activity (β-glucosidase, xylosidase, phenol oxidase, and peroxidase) in peat soils collected from a freshwater forested wetland in coastal North Carolina, USA. Soils were retrieved from three microsites (hummock, hollow, and subsurface peat soils (approximately 20–40 cm below surface)) and incubated at two temperatures (27 °C and 32 °C) and soil water contents (65% and 100% water holding capacity (WHC)). Hummocks had the highest cumulative potential net CO2 (13.7 ± 0.90 mg CO2-C g soil−1) and CH4 (1.8 ± 0.42 mg CH4-C g soil−1) production and enzyme activity, followed by hollows (8.7 ± 0.91 mg CO2-C g soil−1 and 0.5 ± 0.12 mg CH4-C g soil−1) and then subsurface soils (5.7 ± 0.70 mg CO2-C g soil−1 and 0.04 ± 0.019 mg CH4-C g soil−1). Fully saturated soils had lower potential net CO2 production (50–80%) and substantially higher potential net CH4 production compared to non-saturated soils (those incubated at 65% WHC). Soils incubated at 32 °C increased potential net CO2 (24–34%) and CH4 (56–404%) production under both soil moisture levels compared to those incubated at 27 °C. The Q10 values for potential net CO2 and CH4 production ranged from 1.5 to 2.3 and 3.3–8.8, respectively, and did not differ between any microsites or soil water content. Enrichment of δ13CO2-C was found in saturated soils from all microsites (−24.4 to − 29.7 ‰) compared to non-saturated soils (−31.1 to − 32.4 ‰), while δ13CH4-C ranged from −62 to −55‰ in saturated soils. Together, the CO2 and CH4 δ13C data suggest that acetoclastic methanogenesis is an important pathway for CH4 production in these wetlands. A positive relationship (Adj. R2 = 0.40) between peroxidase activity and CH4 production was also found, indicating that peroxidase activity may be important in providing fermented C substrates to acetoclastic methanogenic communities and contribute to anaerobic C mineralization. These results suggest that changes in temperature and hydrology could stimulate CO2 and CH4 emissions from surface hummock soils, and to a lesser extent from hollow soils, and provide preliminary evidence that hummocks may be a spatially important and unrecognized hotspot for CH4 production. |
abstractGer |
Coastal wetlands store significant amounts of carbon (C) belowground, which may be altered through effects of rising temperature and changing hydrology on CO2 and CH4 fluxes and related microbial activities. Wetland microtopography (hummock-hollow) also plays a critical role in mediating plant growth, microbial activity, and thus cycling of C and nutrients and may interact with rising seas to influence coastal wetland C dynamics. Recent evidence suggests that CH4 production in oxygenated surface soils of freshwater wetlands may contribute substantially to global CH4 production, but comprehensive studies linking potential CH4 production to environmental and microbial variables in temperate freshwater forested wetlands are lacking. This study investigated effects of temperature, moisture, and microtopography on potential net CO2 and CH4 production and extracellular enzyme activity (β-glucosidase, xylosidase, phenol oxidase, and peroxidase) in peat soils collected from a freshwater forested wetland in coastal North Carolina, USA. Soils were retrieved from three microsites (hummock, hollow, and subsurface peat soils (approximately 20–40 cm below surface)) and incubated at two temperatures (27 °C and 32 °C) and soil water contents (65% and 100% water holding capacity (WHC)). Hummocks had the highest cumulative potential net CO2 (13.7 ± 0.90 mg CO2-C g soil−1) and CH4 (1.8 ± 0.42 mg CH4-C g soil−1) production and enzyme activity, followed by hollows (8.7 ± 0.91 mg CO2-C g soil−1 and 0.5 ± 0.12 mg CH4-C g soil−1) and then subsurface soils (5.7 ± 0.70 mg CO2-C g soil−1 and 0.04 ± 0.019 mg CH4-C g soil−1). Fully saturated soils had lower potential net CO2 production (50–80%) and substantially higher potential net CH4 production compared to non-saturated soils (those incubated at 65% WHC). Soils incubated at 32 °C increased potential net CO2 (24–34%) and CH4 (56–404%) production under both soil moisture levels compared to those incubated at 27 °C. The Q10 values for potential net CO2 and CH4 production ranged from 1.5 to 2.3 and 3.3–8.8, respectively, and did not differ between any microsites or soil water content. Enrichment of δ13CO2-C was found in saturated soils from all microsites (−24.4 to − 29.7 ‰) compared to non-saturated soils (−31.1 to − 32.4 ‰), while δ13CH4-C ranged from −62 to −55‰ in saturated soils. Together, the CO2 and CH4 δ13C data suggest that acetoclastic methanogenesis is an important pathway for CH4 production in these wetlands. A positive relationship (Adj. R2 = 0.40) between peroxidase activity and CH4 production was also found, indicating that peroxidase activity may be important in providing fermented C substrates to acetoclastic methanogenic communities and contribute to anaerobic C mineralization. These results suggest that changes in temperature and hydrology could stimulate CO2 and CH4 emissions from surface hummock soils, and to a lesser extent from hollow soils, and provide preliminary evidence that hummocks may be a spatially important and unrecognized hotspot for CH4 production. |
abstract_unstemmed |
Coastal wetlands store significant amounts of carbon (C) belowground, which may be altered through effects of rising temperature and changing hydrology on CO2 and CH4 fluxes and related microbial activities. Wetland microtopography (hummock-hollow) also plays a critical role in mediating plant growth, microbial activity, and thus cycling of C and nutrients and may interact with rising seas to influence coastal wetland C dynamics. Recent evidence suggests that CH4 production in oxygenated surface soils of freshwater wetlands may contribute substantially to global CH4 production, but comprehensive studies linking potential CH4 production to environmental and microbial variables in temperate freshwater forested wetlands are lacking. This study investigated effects of temperature, moisture, and microtopography on potential net CO2 and CH4 production and extracellular enzyme activity (β-glucosidase, xylosidase, phenol oxidase, and peroxidase) in peat soils collected from a freshwater forested wetland in coastal North Carolina, USA. Soils were retrieved from three microsites (hummock, hollow, and subsurface peat soils (approximately 20–40 cm below surface)) and incubated at two temperatures (27 °C and 32 °C) and soil water contents (65% and 100% water holding capacity (WHC)). Hummocks had the highest cumulative potential net CO2 (13.7 ± 0.90 mg CO2-C g soil−1) and CH4 (1.8 ± 0.42 mg CH4-C g soil−1) production and enzyme activity, followed by hollows (8.7 ± 0.91 mg CO2-C g soil−1 and 0.5 ± 0.12 mg CH4-C g soil−1) and then subsurface soils (5.7 ± 0.70 mg CO2-C g soil−1 and 0.04 ± 0.019 mg CH4-C g soil−1). Fully saturated soils had lower potential net CO2 production (50–80%) and substantially higher potential net CH4 production compared to non-saturated soils (those incubated at 65% WHC). Soils incubated at 32 °C increased potential net CO2 (24–34%) and CH4 (56–404%) production under both soil moisture levels compared to those incubated at 27 °C. The Q10 values for potential net CO2 and CH4 production ranged from 1.5 to 2.3 and 3.3–8.8, respectively, and did not differ between any microsites or soil water content. Enrichment of δ13CO2-C was found in saturated soils from all microsites (−24.4 to − 29.7 ‰) compared to non-saturated soils (−31.1 to − 32.4 ‰), while δ13CH4-C ranged from −62 to −55‰ in saturated soils. Together, the CO2 and CH4 δ13C data suggest that acetoclastic methanogenesis is an important pathway for CH4 production in these wetlands. A positive relationship (Adj. R2 = 0.40) between peroxidase activity and CH4 production was also found, indicating that peroxidase activity may be important in providing fermented C substrates to acetoclastic methanogenic communities and contribute to anaerobic C mineralization. These results suggest that changes in temperature and hydrology could stimulate CO2 and CH4 emissions from surface hummock soils, and to a lesser extent from hollow soils, and provide preliminary evidence that hummocks may be a spatially important and unrecognized hotspot for CH4 production. |
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<?xml version="1.0" encoding="UTF-8"?><collection xmlns="http://www.loc.gov/MARC21/slim"><record><leader>01000caa a22002652 4500</leader><controlfield tag="001">ELV006497993</controlfield><controlfield tag="003">DE-627</controlfield><controlfield tag="005">20230524145138.0</controlfield><controlfield tag="007">cr uuu---uuuuu</controlfield><controlfield tag="008">230505s2021 xx |||||o 00| ||eng c</controlfield><datafield tag="024" ind1="7" ind2=" "><subfield code="a">10.1016/j.geoderma.2021.115367</subfield><subfield code="2">doi</subfield></datafield><datafield tag="035" ind1=" " ind2=" "><subfield code="a">(DE-627)ELV006497993</subfield></datafield><datafield tag="035" ind1=" " ind2=" "><subfield code="a">(ELSEVIER)S0016-7061(21)00447-X</subfield></datafield><datafield tag="040" ind1=" " ind2=" "><subfield code="a">DE-627</subfield><subfield code="b">ger</subfield><subfield code="c">DE-627</subfield><subfield code="e">rda</subfield></datafield><datafield tag="041" ind1=" " ind2=" "><subfield code="a">eng</subfield></datafield><datafield tag="082" ind1="0" ind2="4"><subfield code="a">550</subfield><subfield code="a">910</subfield><subfield code="q">DE-600</subfield></datafield><datafield tag="084" ind1=" " ind2=" "><subfield code="a">38.60</subfield><subfield code="2">bkl</subfield></datafield><datafield tag="100" ind1="1" ind2=" "><subfield code="a">Minick, Kevan J.</subfield><subfield code="e">verfasserin</subfield><subfield code="4">aut</subfield></datafield><datafield tag="245" ind1="1" ind2="0"><subfield code="a">Wetland microtopography alters response of potential net CO</subfield></datafield><datafield tag="264" ind1=" " ind2="1"><subfield code="c">2021</subfield></datafield><datafield tag="336" ind1=" " ind2=" "><subfield code="a">nicht spezifiziert</subfield><subfield code="b">zzz</subfield><subfield code="2">rdacontent</subfield></datafield><datafield tag="337" ind1=" " ind2=" "><subfield code="a">Computermedien</subfield><subfield code="b">c</subfield><subfield code="2">rdamedia</subfield></datafield><datafield tag="338" ind1=" " ind2=" "><subfield code="a">Online-Ressource</subfield><subfield code="b">cr</subfield><subfield code="2">rdacarrier</subfield></datafield><datafield tag="520" ind1=" " ind2=" "><subfield code="a">Coastal wetlands store significant amounts of carbon (C) belowground, which may be altered through effects of rising temperature and changing hydrology on CO2 and CH4 fluxes and related microbial activities. Wetland microtopography (hummock-hollow) also plays a critical role in mediating plant growth, microbial activity, and thus cycling of C and nutrients and may interact with rising seas to influence coastal wetland C dynamics. Recent evidence suggests that CH4 production in oxygenated surface soils of freshwater wetlands may contribute substantially to global CH4 production, but comprehensive studies linking potential CH4 production to environmental and microbial variables in temperate freshwater forested wetlands are lacking. This study investigated effects of temperature, moisture, and microtopography on potential net CO2 and CH4 production and extracellular enzyme activity (β-glucosidase, xylosidase, phenol oxidase, and peroxidase) in peat soils collected from a freshwater forested wetland in coastal North Carolina, USA. Soils were retrieved from three microsites (hummock, hollow, and subsurface peat soils (approximately 20–40 cm below surface)) and incubated at two temperatures (27 °C and 32 °C) and soil water contents (65% and 100% water holding capacity (WHC)). Hummocks had the highest cumulative potential net CO2 (13.7 ± 0.90 mg CO2-C g soil−1) and CH4 (1.8 ± 0.42 mg CH4-C g soil−1) production and enzyme activity, followed by hollows (8.7 ± 0.91 mg CO2-C g soil−1 and 0.5 ± 0.12 mg CH4-C g soil−1) and then subsurface soils (5.7 ± 0.70 mg CO2-C g soil−1 and 0.04 ± 0.019 mg CH4-C g soil−1). Fully saturated soils had lower potential net CO2 production (50–80%) and substantially higher potential net CH4 production compared to non-saturated soils (those incubated at 65% WHC). Soils incubated at 32 °C increased potential net CO2 (24–34%) and CH4 (56–404%) production under both soil moisture levels compared to those incubated at 27 °C. The Q10 values for potential net CO2 and CH4 production ranged from 1.5 to 2.3 and 3.3–8.8, respectively, and did not differ between any microsites or soil water content. Enrichment of δ13CO2-C was found in saturated soils from all microsites (−24.4 to − 29.7 ‰) compared to non-saturated soils (−31.1 to − 32.4 ‰), while δ13CH4-C ranged from −62 to −55‰ in saturated soils. Together, the CO2 and CH4 δ13C data suggest that acetoclastic methanogenesis is an important pathway for CH4 production in these wetlands. A positive relationship (Adj. R2 = 0.40) between peroxidase activity and CH4 production was also found, indicating that peroxidase activity may be important in providing fermented C substrates to acetoclastic methanogenic communities and contribute to anaerobic C mineralization. These results suggest that changes in temperature and hydrology could stimulate CO2 and CH4 emissions from surface hummock soils, and to a lesser extent from hollow soils, and provide preliminary evidence that hummocks may be a spatially important and unrecognized hotspot for CH4 production.</subfield></datafield><datafield tag="650" ind1=" " ind2="4"><subfield code="a">Methanogenesis</subfield></datafield><datafield tag="650" ind1=" " ind2="4"><subfield code="a">Anaerobic respiration</subfield></datafield><datafield tag="650" ind1=" " ind2="4"><subfield code="a">Peat</subfield></datafield><datafield tag="650" ind1=" " ind2="4"><subfield code="a">Stable carbon isotopes</subfield></datafield><datafield tag="650" ind1=" " ind2="4"><subfield code="a">Extracellular enzyme activity</subfield></datafield><datafield tag="650" ind1=" " ind2="4"><subfield code="a">forested wetland</subfield></datafield><datafield tag="700" ind1="1" ind2=" "><subfield code="a">Mitra, Bhaskar</subfield><subfield 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