Methane Release Driven by Algae Vital Activity

Main Article Content

Hui Liang

Abstract

As a potent greenhouse gas, accurate estimation and regulation of methane's global emission budget is the key to addressing climate change. Conventional wisdom suggests that methane production is mainly confined to anaerobic environments, but recent studies have confirmed that algae can drive methane release through a variety of pathways. Although the current research clarifies the important role of algae in the methane cycle, it still faces challenges such as difficulty in quantifying the ecological contribution rate of each release pathway and unclear key molecular mechanisms. In-depth exploration of the laws and mechanisms of algae-driven methane release can not only improve the theoretical framework of the global methane cycle, but also provide scientific basis and new perspectives for ecosystem greenhouse gas emission control and carbon cycle regulation.

Article Details

How to Cite
Liang , H. (2026). Methane Release Driven by Algae Vital Activity. Journal of Research in Multidisciplinary Methods and Applications, 5(3), 01260503003. Retrieved from http://www.satursonpublishing.com/jrmma/article/view/a01260503003
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References

KEES V D G, ROMY V D B. Slow-onset events: a review of the evidence from the IPCC Special Reports on Land, Oceans and Cryosphere [J]. Current Opinion in Environmental Sustainability, 2021, 50: 109–20.

Climate Change 2021—The Physical Science Basis [J]. Chemistry International, 2021, 43(4): 22–3.

Moving Beyond Global Warming Potentials to Quantify the Climatic Role of Ecosystems [J]. Ecosystems, 2015, 18(6): 1000–13.

ZHANG Bo, TANG Xu. Towards "carbon neutrality", methane emission reduction cannot be ignored [N]. 2021–01–04.

XU H, LI H, TANG Z, et al. Underestimated methane production triggered by phytoplankton succession in river-reservoir systems: Evidence from a microcosm study [J]. Water Research, 2020, 185: 116233.

ZHANG M, XIAO Q, ZHANG Z, et al. Methane flux dynamics in a submerged aquatic vegetation zone in a subtropical lake [J]. Science of the Total Environment, 2019, 672: 400–9.

WEI L, XIAOKUN H, CONGQIANG L, et al. Sulfate concentrations affect sulfate reduction pathways and methane consumption in coastal wetlands [J]. Water research, 2022, 217: 118441–.

Niu Mingyang, Liang Wenyue, Wang Fengping. Biotransformation of methane in marine environment and its impact on climate change [J]. Science in China: Earth Sciences, 2018, 48(12): 1568–88.

DIMITAR K, J B D, ERIC T, et al. Acetate oxidation is the dominant methanogenic pathway from acetate in the absence of Methanosaetaceae [J]. Applied and environmental microbiology, 2006, 72(7): 5138–41.

Mai Fuyuan, Tong Yindong, Zhang Qianggong, et al. Research progress on methane release characteristics and influencing factors in lakes [J]. Journal of Agricultural Resources and Environment, 2024, 41(03): 677–87.

TANG K W, MCGINNIS D F, IONESCU D. Methane Production in Oxic Lake Waters Potentially Increases Aquatic Methane Flux to Air [J]. Environmental Science & Technology Letters, 2016, 3(6): 227–33.

LIU Yili, LI Zhulin, HE Yunfeng. Research progress on factors affecting methane production, transport and oxidation in wetlands [J]. Journal of Northwest A&F University(Natural Science Edition), 2014, 42(09): 157–62.

J L H. Methane emission from natural wetlands: interplay between emergent macrophytes and soil microbial processes. A mini-review [J]. Annals of botany, 2010, 105(1): 141–53.

LI T, RAIVONEN M, ALEKSEYCHIK P, et al. Importance of vegetation classes in modeling CH 4 emissions from boreal and subarctic wetlands in Finland [J]. Science of the Total Environment, 2016, 572: 1111–22.

BIAN R, KOMIYA T, SHIMAOKA T, et al. Simulative analysis of vegetation on CH 4 emission from landfill cover soils: Combined effects of root-water uptake, root radial oxygen loss, and plant-mediated CH 4 transport [J]. Journal of Cleaner Production, 2019, 234: 18–26.

CHARLOTTE G, GWENAëL A, RAQUEL M, et al. The transformation of macrophyte-derived organic matter to methane relates to plant water and nutrient contents [J]. Limnology and oceanography, 2019, 64(4): 1737–49.

PRANAS B, ANTONAS M. Biogas production experimental research using algae [J]. Journal of environmental health science & engineering, 2015, 13(1): 18.

Li Ke, Guan Baohua, Liu Zhengwen. Experimental analysis of detritus decomposition rate and nitrogen and phosphorus release mode of cyanobacterial [J]. Lake Science, 2011, 23(06): 919–25.

Shang Lixia, Ke Fan, Li Wenchao, et al. Experimental study on anaerobic decomposition process and pollutant release of high-density cyanobacteria [J]. Lake Science, 2013, 25(01): 47–54.

HE W, SHANG J, LU X, et al. Effects of sludge dredging on the prevention and control of algae-caused black bloom in Taihu Lake, China [J]. Journal of Environmental Sciences, 2013, 25(3): 430–40.

WANG Y, CHEN F. Decomposition and phosphorus release from four different size fractions of Microcystis spp. taken from Lake Taihu, China [J]. Journal of Environmental Sciences, 2008, 20(7): 891–6.

ZHANG Y, DIJK M A V, LIU M, et al. The contribution of phytoplankton degradation to chromophoric dissolved organic matter (CDOM) in eutrophic shallow lakes: Field and experimental evidence [J]. Water Research, 2009, 43(18): 4685–97.

Lu Xiaoyou, Liu Hongbo, Huang Fang, et al. Reduction and resource utilization of cyanobacterial algae mud in Taihu Lake by anaerobic fermentation to produce volatile fatty acids [J]. Transactions of the CSAE, 2020, 14(05): 1376–84.

PERGA M E, MABERLY S C, JENNY J P, et al. A century of human‐driven changes in the carbon dioxide concentration of lakes [J]. Global Biogeochemical Cycles, 2016, 30(2): 93–104.

Productivity and depth regulate lake contributions to atmospheric methane [J]. Limnology and Oceanography, 2016, 61(S1): S51–S61.

XIAO Q, ZHANG M, HU Z, et al. Spatial variations of methane emission in a large shallow eutrophic lake in subtropical climate [J]. Journal of Geophysical Research: Biogeosciences, 2017, 122(7): 1597–614.

Xiao Qitao, Liao Yuanshan, Liu Zhenjing, et al. Characteristics of dissolved organic carbon in algae lakes and their effects on methane emissions [J]. Journal of Nanjing University of Information Science and Technology(Natural Science Edition), 2022, 14(01): 21–31.

Effects of sulfate in eutrophicated lakes on methanogenesis of cyanobacterial decay [J]. Limnological Science, 2021, 33(06): 1639–49.

Liu Yi, Xu Haolian, Mao Yufeng, et al. Methanogenesis dynamics and key influencing factors during the decline of Aeruginosa aeruginosa [J]. Transactions of the Chinese Society of Civil and Environmental Engineering(Chinese and English), 2019, 41(05): 132–40.

JING W, ZHI-PENG W, YI-XUAN C, et al. Eutrophic levels and algae growth increase emissions of methane and volatile sulfur compounds from lakes [J]. Environmental Pollution, 2022, 306: 119435–.

STANISLAVA M, R W A, RUTH F. Influence of NH3 and NH4+ on anaerobic digestion and microbial population structure at increasing total ammonia nitrogen concentrations [J]. Bioresource technology, 2022, 361: 127638–.

CéLINE L, POLETTE A-M, NATALIA C, et al. Temperature differently affected methanogenic pathways and microbial communities in sub-Antarctic freshwater ecosystems [J]. Environment International, 2021, 154: 106575–.

MENG S, BING L, KATSUNORI Y, et al. Effects of low pH conditions on decay of methanogenic biomass [J]. Water Research, 2020, 179: 115883.

ZHANG Xiuyun, LIANG Xia, HE Chiquan. Research progress on the effects of macrofilamentous algae on methane emissions in urban rivers [J]. Chinese Journal of Applied Ecology, 2013, 24(05): 1291–9.

HUERTOS M L, GENTRY L E, SHENNAN C. Land Use and Stream Nitrogen Concentrations in Agricultural Watersheds Along the Central Coast of California [J]. The Scientific World Journal, 2001, 1: 615–22.

CHUANQIAO Z, YU P, MIAOTONG Y, et al. Severe cyanobacteria accumulation potentially induces methylotrophic methane producing pathway in eutrophic lakes [J]. Environmental Pollution, 2022, 292(PB): 118443–.

GRID.38678.32, DéPARTEMENT DES SCIENCES BIOLOGIQUES, GROUPE DE RECHERCHE INTERUNIVERSITAIRE EN LIMNOLOGIE ET EN ENVIRONNEMENT AQUATIQUE , UNIVERSITé DU QUéBEC à MONTRéAL, MONTRéAL, QUéBEC, CANADA, GRID.224260.0, DEPARTMENT OF BIOLOGY, ENVIRONMENTAL STUDIES V C U, RICHMOND, VA, USA, et al. Selective consumption and metabolic allocation of terrestrial and algal carbon determine allochthony in lake bacteria [J]. The ISME journal, 2016, 10(6): 1373–82.

NEAL C, HOUSE W A, JARVIE H P, et al. The water quality of the River Dun and the Kennet and Avon Canal [J]. Journal of Hydrology, 2006, 330(1-2): 155–70.

TONG J, XUERONG W, TINGYAN G, et al. Litter Decomposition of Imperata cylindrica in a Copper Tailing Areas With Different Restoration History: Fungal Community Dynamics and Driving Factors [J]. Frontiers in Microbiology, 2021, 12: 780015–.

BORREL G, JéZéQUEL D, BIDERRE-PETIT C, et al. Production and consumption of methane in freshwater lake ecosystems [J]. Research in Microbiology, 2011, 162(9): 832–47.

SHUWEI L, ZHIQIANG H, SHUANG W, et al. Methane and Nitrous Oxide Emissions Reduced Following Conversion of Rice Paddies to Inland Crab-Fish Aquaculture in Southeast China [J]. Environmental science & technology, 2016, 50(2): 633–42.

XI X, SUSANA A, FANG L, et al. Nutrient removal from Chinese coastal waters by large-scale seaweed aquaculture [J]. Scientific reports, 2017, 7(1-4): 46613.

LIIKANEN A, MURTONIEMI T, TANSKANEN H, et al. Effects of Temperature and Oxygen Availability on Greenhouse Gas and Nutrient Dynamics in Sediment of a Eutrophic Mid-Boreal Lake [J]. Biogeochemistry, 2002, 59(3): 269–86.

ZHIQIANG H, SHUANG W, CHENG J, et al. A comparison of methane emissions following rice paddies conversion to crab-fish farming wetlands in southeast China [J]. Environmental science and pollution research international, 2016, 23(2): 1505–15.

HANS-PETER G, KATHARINA F, CLAUDIA D, et al. Microbial methane production in oxygenated water column of an oligotrophic lake [J]. Proceedings of the National Academy of Sciences of the United States of America, 2011, 108(49): 19657–61.

DIAZ R J, ROSENBERG R. Spreading Dead Zones and Consequences for Marine Ecosystems [J]. Science, 2008, 321(5891): 926–9.

LIU S, FENG W, SONG F, et al. Photodegradation of algae and macrophyte-derived dissolved organic matter: A multi-method assessment of DOM transformation [J]. Limnologica, 2019, 77: 125683–.

YAN X, XU X, JI M, et al. Cyanobacteria blooms: A neglected facilitator of CH 4 production in eutrophic lakes [J]. Science of the Total Environment, 2019, 651(P1): 466–74.

FUCHS A, LYAUTEY E, MONTUELLE B, et al. Effects of increasing temperatures on methane concentrations and methanogenesis during experimental incubation of sediments from oligotrophic and mesotrophic lakes [J]. Journal of Geophysical Research: Biogeosciences, 2016, 121(5): 1394–406.

GRID.411173.1, DEPARTMENT OF GEOGRAPHY, SEDIMENTARY, ENVIRONMENTAL PROCESSES LABORATORY I O G, UNIVERSIDADE FEDERAL FLUMINENSE, 24210-346 NITERóI, BRAZIL, GRID.. 8 X, INTERNATIONAL LABORATORY OF CLIMATIC CHANGE , UNIVERSIDADE FEDERAL DO RIO DE JANEIRO, 68020 RIO DE JANEIRO, BRAZIL, et al. Greenhouse gas production in low-latitude lake sediments responds strongly to warming [J]. Nature Climate Change, 2014, 4(6): 467–70.

Hu Peng, Yang Qing, Yang Zefan, et al. Experimental study on dissolved oxygen content and its physical influencing factors in water [J]. Journal of Water Resources, 2019, 50(06): 679–86.

Lin Hai, Zhou Gang, Li Xuguang, et al. Greenhouse gas emissions and comprehensive warming potential of Chinese velvet crab ecosystem in summer pond farming [J]. Journal of Fisheries Sciences, 2013, 37(03): 417–24.

R K O, W F M, V S M, et al. shift from acetoclastic to H2-dependent methanogenesis in a west Siberian peat bog at low pH values and isolation of an acidophilic Methanobacterium strain [J]. Applied and environmental microbiology, 2007, 73(7): 2344–8.

LOUIS V L S, KELLY C A, EACUTE, et al. Reservoir Surfaces as Sources of Greenhouse Gases to the Atmosphere: A Global Estimate [J]. BioScience, 2000, 50(9): 766–75.

LOFTON D D, WHALEN S C, HERSHEY A E. Effect of temperature on methane dynamics and evaluation of methane oxidation kinetics in shallow Arctic Alaskan lakes [J]. Hydrobiologia, 2014, 721(1): 209–22.

SHELLEY F, ABDULLAHI F, GREY J, et al. Microbial methane cycling in the bed of a chalk river: oxidation has the potential to match methanogenesis enhanced by warming [J]. Freshwater Biology, 2015, 60(1): 150–60.

LUO G J, KIESE R, WOLF B, et al. Effects of soil temperature and moisture on methane uptake and nitrous oxide emissions across three different ecosystem types [J]. Biogeosciences, 2013, 10(5): 3205–19.

Liu Chunguang, Jin, Sun Ling, Zhong Yuan, Dai Shugui, Zhuang Yuanyi. Effects of pH on Growth and Species Changes of Freshwater Algae [J]. Journal of Agricultural and Environmental Sciences, 2005, (02): 294–8.

Han Yang. Research on greenhouse gas emission flux and its influencing factors in rivers in Nanjing [D]; Nanjing University of Information Science and Technology, 2013.

Gu Hang, Xiao Fanshu, He Zhili, et al. Microbial-mediated methane emission mechanism in wetlands [J]. Acta Microbiology, 2018, 58(04): 618–32.

STANLEY E H, POWERS S M, LOTTIG N R, et al. Contemporary changes in dissolved organic carbon (DOC) in human‐dominated rivers: is there a role for DOC management? [J]. Freshwater Biology, 2012, 57: 26–42.

CAROLYN-MONIKA G, RALF C, O P S. Effect of soil properties and hydrology on archaeal community composition in three temperate grasslands on peat [J]. FEMS microbiology ecology, 2013, 85(2): 227–40.

Zhang Jin, Chen Mingying, Hao Zhizhi, et al. Dynamic changes of dissolved organic matter produced by algal bloom decomposition in eutrophicated lakes and their environmental effects [J]. Environmental Science, 2024, 45(03): 1539–52.

NGO A V, NGUYEN H T, LE C V, et al. A dynamic simulation of methane fermentation process receiving heterogeneous food wastes and modelling acidic failure [J]. Journal of Material Cycles and Waste Management, 2016, 18(2): 239–47.

Comparative study on the decomposition process of several aquatic plants [J]. Chinese Journal of Ecology, 2014, 34(14): 3848–58.

Meng Zejing, Li Yucheng, Wu Juan, et al. Laboratory simulation study on color and morphological changes during the decline of Chaohu cyanobacteria [J]. Anhui Agricultural Sciences, 2011, 39(17): 10348–52.

Li Yonghui, Li Yucheng, Wang Ning, et al. Formation of typical harmful components and control measures during the death and decay of Chaohu cyanobacteria [J]. Lake Science, 2012, 24(04): 513–8.

SHANGBIN X, DEFU L, YUCHUN W, et al. Temporal variation of methane flux from Xiangxi Bay of the Three Gorges Reservoir [J]. Scientific reports, 2013, 3(1): 2500.

YU Q, CHANGYUE O, YUJIA G, et al. The characteristics and influencing factors of dissolved methane concentrations in Chongqing's central urban area in the Three Gorges Reservoir, China [J]. Environmental science and pollution research international, 2022, 29(47): 72045–57.

XIONG Y, ZHOU J, CHEN L, et al. Land Use Pattern and Vegetation Cover Dynamics in the Three Gorges Reservoir (TGR) Intervening Basin [J]. Water, 2020, 12(7).

DEEMER B R, HARRISON J A, LI S, et al. Greenhouse Gas Emissions from Reservoir Water Surfaces: A New Global Synthesis [J]. Bioscience, 2016, 66(11): 949–.

A D T, JOACHIM A, JENS-CHRISTIAN S, et al. Eutrophication effects on greenhouse gas fluxes from shallow-lake mesocosms override those of climate warming [J]. Global change biology, 2015, 21(12): 4449–63.

XIAO M, LI M, DUAN P, et al. Insights into the relationship between colony formation and extracellular polymeric substances (EPS) composition of the cyanobacterium Microcystis spp [J]. Harmful Algae, 2019, 83: 34–41.

VAN DEN MEERSCHE K, MIDDELBURG J J, SOETAERT K, et al. Carbon-nitrogen coupling and algal-bacterial interactions during an experimental bloom: Modeling a 13C tracer experiment [J]. Limnology and Oceanography, 2004, 49(3): 862–78.

SHI L, HUANG Y, ZHANG M, et al. Bacterial community dynamics and functional variation during the long-term decomposition of cyanobacterial blooms in-vitro [J]. Science of the Total Environment, 2017, 598: 77–86.

KDODDS W, HSMITH V, KIRKLOHMAN. Erratum: Nitrogen and phosphorus relationships to benthic algal biomass in temperate streams [J]. Canadian Journal of Fisheries and Aquatic Sciences, 2006, 63(5): 1190–1.

Changes of planktonic algae community under different nitrogen and phosphorus ratios [J]. Chinese Journal of Applied Ecology, 2006, (07): 1218–23.

Chen Chongjun, Chen Chongjun, Han Zhiying, et al. Zhou Cong algae and their application in water purification [J]. Chinese Journal of Applied Ecology, 2009, 20(11): 2820–6.

LINGLI L, L G T. A review of nitrogen enrichment effects on three biogenic GHGs: the CO2 sink may be largely offset by stimulated N2O and CH4 emission [J]. Ecology letters, 2009, 12(10): 1103–17.

STAPLETON L M, CROUT N M J, SäWSTRöM C, et al. Microbial carbon dynamics in nitrogen amended Arctic tundra soil: Measurement and model testing [J]. Soil Biology and Biochemistry, 2005, 37(11): 2088–98.

BODELIER P L E, LAANBROEK H J. Nitrogen as a regulatory factor of methane oxidation in soils and sediments [J]. FEMS Microbiology Ecology, 2004, 47(3): 265–77.

FRANCESC S D V M E R J L S. Effects of nutrients and light on periphyton biomass and nitrogen uptake in Mediterranean streams with contrasting land uses [J]. Freshwater Biology, 2007, 52(5): 891–906.

LI Lingling, XUE Bin, YAO Shuchun. Significance and application of methane generation and oxidation in lake sediments [J]. Bulletin of Mineral and Rock Geochemistry, 2016, 35(04): 634–45+07.

J. T L, A. D J, B. C J, et al. Lakes and Reservoirs as Regulators of Carbon Cycling and Climate [J]. Limnology and Oceanography, 2009, 54(6): 2298–314.

KAYRANLI B. Carbon Storage and Fluxes within Freshwater Wetlands: a Critical Review [J]. Wetlands: The Journal of the Society of Wetland Scientists, 2010, 30(1): p.111–p.

K K J. Wetlands and the global carbon cycle: what might the simulated past tell us about the future? [J]. The New phytologist, 2011, 192(4): 789–92.

CONRAD R. Contribution of hydrogen to methane production and control of hydrogen concentrations in methanogenic soils and sediments [J]. FEMS Microbiology Ecology, 1999, 28(3): 193–202.

H W K, R T M, R R A, et al. Contributions of algae to GPP and DOC production in an Alaskan fen: effects of historical water table manipulations on ecosystem responses to a natural flood [J]. Oecologia, 2012, 169(3): 821–32.

WEST W, COLOSO J, JONES S. Effects of algal and terrestrial carbon on methane production rates and [J]. Freshwater Biology, 2012, 57(5): 949–55.

HE Z, WANG J, HU J, et al. Regulation of coastal methane sinks by a structured gradient of microbial methane oxidizers [J]. Environmental Pollution, 2018, 244: 228–37.

SCHOLTEN J C M, BODEGOM P M V, VOGELAAR J, et al. Effect of sulfate and nitrate on acetate conversion by anaerobic microorganisms in a freshwater sediment [J]. FEMS Microbiology Ecology, 2002, 42(3): 375–85.

SCHEID D, STUBNER S, CONRAD R. Effects of nitrate- and sulfate-amendment on the methanogenic populations in rice root incubations [J]. FEMS Microbiology Ecology, 2003, 43(3): 309–15.