热带浅海沉积物中的甲烷生成
Methane production in shallow-water, tropical marine sediments.
作者信息
Oremland R S
出版信息
Appl Microbiol. 1975 Oct;30(4):602-8. doi: 10.1128/am.30.4.602-608.1975.
Abstract
The in situ production of methane was monitored in several types of tropical benthic communities. A bed of Thalassia testudinum located in Caesar Creek (Florida Keys) exhibited the highest methanogenic activity (initial rates = 1.81 to 1.86 mumol CH4/m2 per h) as compared with another seagrass (Syringodium sp., 0.15 to 0.33 mumol/m2 per h) and two coral reef environments (Hydro-Lab, 0.016 to 0.10 mumol/m2 per h; Curacao, 0.14 to 0.47 mumol/m2 per h). The results suggest that a wide variety of benthic metabolic processes (e.g., photosynthetic oxygen production) influences methane production rates.
摘要
对几种热带底栖生物群落中的甲烷原位生成情况进行了监测。位于凯撒溪（佛罗里达群岛）的一片泰来藻床表现出最高的产甲烷活性（初始速率为每小时1.81至1.86 μmol CH₄/m²），与之相比，另一种海草（Syringodium sp.，每小时0.15至0.33 μmol/m²）以及两个珊瑚礁环境（Hydro-Lab，每小时0.016至0.10 μmol/m²；库拉索岛，每小时0.14至0.47 μmol/m²）的产甲烷活性较低。结果表明，多种底栖生物代谢过程（如光合产氧）会影响甲烷生成速率。
相似文献
1
Methane production in shallow-water, tropical marine sediments.
Appl Microbiol. 1975 Oct;30(4):602-8. doi: 10.1128/am.30.4.602-608.1975.
2
Inhibition of methanogenesis in marine sediments by acetylene and ethylene: validity of the acetylene reduction assay for anaerobic microcosms.
Appl Microbiol. 1975 Oct;30(4):707-9. doi: 10.1128/am.30.4.707-709.1975.
3
[The biogeochemical cycle of methane in the coastal zone and littoral of the Kandalaksha Bay of the White Sea].
Mikrobiologiia. 2004 Jul-Aug;73(4):540-52.
4
Tropical species at the northern limit of their range: composition and distribution in Bermuda's benthic habitats in relation to depth and light availability.
Mar Environ Res. 2013 Aug;89:63-75. doi: 10.1016/j.marenvres.2013.05.003. Epub 2013 May 16.
5
Effect of sulfate on carbon and electron flow during microbial methanogenesis in freshwater sediments.
Appl Environ Microbiol. 1977 Feb;33(2):275-81. doi: 10.1128/aem.33.2.275-281.1977.
6
Anaerobic metabolism of immediate methane precursors in Lake Mendota.
Appl Environ Microbiol. 1979 Feb;37(2):244-53. doi: 10.1128/aem.37.2.244-253.1979.
7
Thalassic biogas production from sea wrack biomass using different microbial seeds: cow manure, marine sediment and sea wrack-associated microflora.
Bioresour Technol. 2013 Apr;133:612-7. doi: 10.1016/j.biortech.2013.01.082. Epub 2013 Feb 6.
8
Microbial biomass and productivity in seagrass beds.
Geomicrobiol J. 1985;4(1):21-51. doi: 10.1080/01490458509385919.
9
[Bacterial processes of the methane cycle in the bottom sediments of Baikal lake].
Mikrobiologiia. 2004 Mar-Apr;73(2):248-57.
10
Association of hydrogen metabolism with methanogenesis in Lake Mendota sediments.
Appl Environ Microbiol. 1977 Feb;33(2):312-8. doi: 10.1128/aem.33.2.312-318.1977.
引用本文的文献
1
Got acetylene: a personal research retrospective.
FEMS Microbes. 2021 Jul 31;2:xtab009. doi: 10.1093/femsmc/xtab009. eCollection 2021.
2
Diverse methylotrophic methanogenic archaea cause high methane emissions from seagrass meadows.
Proc Natl Acad Sci U S A. 2022 Mar 1;119(9). doi: 10.1073/pnas.2106628119.
3
Methane emission and sulfide levels increase in tropical seagrass sediments during temperature stress: A mesocosm experiment.
Ecol Evol. 2020 Feb 5;10(4):1917-1928. doi: 10.1002/ece3.6009. eCollection 2020 Feb.
4
Methane production in Minnesota peatlands.
Appl Environ Microbiol. 1984 Jun;47(6):1266-71. doi: 10.1128/aem.47.6.1266-1271.1984.
5
Competition for sulfate and ethanol among desulfobacter, desulfobulbus, and desulfovibrio species isolated from intertidal sediments.
Appl Environ Microbiol. 1984 Feb;47(2):329-34. doi: 10.1128/aem.47.2.329-334.1984.
6
Substrates for sulfate reduction and methane production in intertidal sediments.
Appl Environ Microbiol. 1983 Jan;45(1):193-9. doi: 10.1128/aem.45.1.193-199.1983.
7
Denitrification associated with periphyton communities.
Appl Environ Microbiol. 1981 Oct;42(4):745-8. doi: 10.1128/aem.42.4.745-748.1981.
8
Microbial formation of ethane in anoxic estuarine sediments.
Appl Environ Microbiol. 1981 Jul;42(1):122-9. doi: 10.1128/aem.42.1.122-129.1981.
9
Comparison of in situ and in vitro rates of methane release in freshwater sediments.
Appl Environ Microbiol. 1980 Aug;40(2):287-93. doi: 10.1128/aem.40.2.287-293.1980.
10
Populations of methane-producing bacteria and in vitro methanogenesis in salt marsh and estuarine sediments.
Appl Environ Microbiol. 1980 Apr;39(4):864-71. doi: 10.1128/aem.39.4.864-871.1980.
本文引用的文献
1
Methane production in the interstitial waters of sulfate-depleted marine sediments.
Science. 1974 Sep 27;185(4157):1167-9. doi: 10.1126/science.185.4157.1167.
2
Inhibition of rumen methanogenesis by methane analogues.
J Bacteriol. 1967 Jul;94(1):171-5. doi: 10.1128/jb.94.1.171-175.1967.
3
Biological methylation of mercury in aquatic organisms.
Nature. 1969 Aug 16;223(5207):753-4. doi: 10.1038/223753a0.
4
Synthesis of methyl-mercury compounds by extracts of a methanogenic bacterium.
Nature. 1968 Oct 12;220(5163):173-4. doi: 10.1038/220173a0.
5
Microbial formation of methane.
Adv Microb Physiol. 1971;6:107-46. doi: 10.1016/s0065-2911(08)60068-5.
6
Microbial growth rates in nature.
Bacteriol Rev. 1971 Mar;35(1):39-58. doi: 10.1128/br.35.1.39-58.1971.
7
Interrelations between sulfate-reducing and methane-producing bacteria in bottom deposits of a fresh-water lake. I. Field observations.
Antonie Van Leeuwenhoek. 1974;40(2):285-95. doi: 10.1007/BF00394387.
Zotero 插件