Articles | Volume 20, issue 19
https://doi.org/10.5194/bg-20-4029-2023
© Author(s) 2023. This work is distributed under
the Creative Commons Attribution 4.0 License.
the Creative Commons Attribution 4.0 License.
https://doi.org/10.5194/bg-20-4029-2023
© Author(s) 2023. This work is distributed under
the Creative Commons Attribution 4.0 License.
the Creative Commons Attribution 4.0 License.
Carbon dioxide and methane fluxes from mounds of African fungus-growing termites
Department of Geosciences and Geography, University of Helsinki,
P.O. Box 64, 00014, Helsinki, Finland
Risto Vesala
Finnish Museum of Natural History, University of Helsinki, P.O. Box
64, 00014, Helsinki, Finland
Petri Rönnholm
Department of Built Environment, Aalto University, P.O. Box 14100,
00076, Aalto, Finland
Laura Arppe
Finnish Museum of Natural History, University of Helsinki, P.O. Box
64, 00014, Helsinki, Finland
Petra Manninen
Department of Geosciences and Geography, University of Helsinki,
P.O. Box 64, 00014, Helsinki, Finland
Markus Jylhä
Department of Geosciences and Geography, University of Helsinki,
P.O. Box 64, 00014, Helsinki, Finland
Jouko Rikkinen
Finnish Museum of Natural History, University of Helsinki, P.O. Box
64, 00014, Helsinki, Finland
Organismal and Evolutionary Biology Research Programme, Faculty of
Biological and Environmental Sciences, P.O. Box 64, 00014, Helsinki, Finland
Petri Pellikka
Department of Geosciences and Geography, University of Helsinki,
P.O. Box 64, 00014, Helsinki, Finland
Wangari Maathai Institute for Environmental and Peace Studies,
University of Nairobi, P.O. Box 29053, 00625, Kangemi, Kenya
Janne Rinne
Natural Resources Institute Finland, P.O. Box 2, 00791 Helsinki,
Finland
Department of Physical Geography and Ecosystem Science, Lund
University, Lund, Sweden
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Cited articles
Agarwal, V. B.: Temperature and relative humidity inside the mound of
Odontotermes obesus (Rambur) (Isoptera: Termitidae), Proc. Anim. Sci., 89, 91–99, https://doi.org/10.1007/BF03179148,
1980.
Amara, E., Adhikari, H., Heiskanen, J., Siljander, M., Munyao, M., Omondi,
P., and Pellikka, P.: Aboveground Biomass Distribution in a Multi-Use
Savannah Landscape in Southeastern Kenya: Impact of Land Use and Fences,
Land, 9, 381, https://doi.org/10.3390/land9100381, 2020.
Bagine, R., Brandl, R., and Kaib, M.: Species Delimitation in Macrotermes
(Isoptera: Macrotermitidae): Evidence from Epicuticular Hydrocarbons,
Morphology, and Ecology, Ann. Entom. Soc. Am., 87,
498–506, 1994.
Bignell, D. E. and Eggleton, P.: Termites in ecosystems, in Termites:
Evolution, Sociality, Symbioses and Ecology, edited by: Abe, T., Bignell, D. E.,
and Higashi, M., Springer, 363–387, 2000.
Boutton, T. W., Arshad, M. A., and Tieszen, L. L.: Stable isotope analysis of
termite food habits in East African grasslands, Oecologia, 59, 1–6,
https://doi.org/10.1007/BF00388065, 1983.
Brümmer, C., Papen, H., Wassmann, R., and Brüggemann, N.: Fluxes of
CH4 and CO2 from soil and termite mounds in south Sudanian savanna
of Burkina Faso (West Africa), Global Biogeochem. Cy., 23, 1,
https://doi.org/10.1029/2008GB003237, 2009.
Buxton, R. D.: Termites and the turnover of dead wood in an arid tropical
environment, Oecologia, 51, 379–384, https://doi.org/10.1007/BF00540909, 1981.
Chen, C., Wu, J., Zhu, X., Jiang, X., Liu, W., Zeng, H., and Meng, F.-R.:
Hydrological characteristics and functions of termite mounds in areas with
clear dry and rainy seasons, Agriculture, Ecosyst. Environ., 277,
25–35, https://doi.org/10.1016/j.agee.2019.03.001, 2019.
Chiri, E., Greening, C., Lappan, R., Waite, D. W., Jirapanjawat, T., Dong,
X., Arndt, S. K., and Nauer, P. A.: Termite mounds contain soil-derived
methanotroph communities kinetically adapted to elevated methane
concentrations, ISME J., 14, 2715–2731, https://doi.org/10.1038/s41396-020-0722-3,
2020.
Collins, N. M.: The role of termites in the decomposition of wood
and leaf litter in the Southern Guinea savanna of Nigeria, Oecologia,
51, 389–399, https://doi.org/10.1007/BF00540911, 1981.
Darlington, J. P. E. C.: The underground passages and storage pits used in
foraging by a nest of the termite Macrotermes michaelseni in Kajiado, Kenya,
J. Zoology, 198, 237–247,
https://doi.org/10.1111/j.1469-7998.1982.tb02073.x, 1982.
Darlington, J. P. E. C.: A method for sampling the populations of large
termite nests, Ann. Appl. Biol., 104, 427–436, 1984.
Darlington, J. P. E. C.: Structure of mature mounds of the termite
Macrotermes michaelseni in Kenya, Int. J. Trop. Insect
Sci., 6, 149–156, https://doi.org/10.1017/S1742758400006536,
1985.
Darlington, J. P. E. C.: Seasonality in mature nests of the termite
Macrotermes michaelseni in Kenya, Insectes Sociaux, 33, 168–189, 1986.
Darlington, J. P. E. C.: Populations in nests of the termite Macrotermes
subhyalinus in Kenya, Insectes Sociaux, 37, 158–168,
https://doi.org/10.1007/BF02224028, 1990.
Darlington, J. P. E. C. and Dransfield, R. D.: Size relationships in nest
populations and mound parameters in the termite Macrotermes michaelseni in
Kenya, Insectes Sociaux, 34, 165–180, 1987.
Darlington, J. P. E. C., Zimmerman, P. R., Greenberg, J., Westberg, C., and
Bakwin, P.: Production of metabolic gases by nests of the termite
Macrotermes jeanneli in Kenya, J. Trop. Ecol., 13, 491–510,
https://doi.org/10.1017/S0266467400010671, 1997.
Eggleton, P. and Tayasu, I.: Feeding groups, lifetypes and the global
ecology of termites, Ecol. Res., 16, 941–960,
https://doi.org/10.1046/j.1440-1703.2001.00444.x, 2001.
Higashi, M., Abe, T., and Burns, T. P.: Carbon-nitrogen balance and termite
ecology, P. Roy. Soc. B-Bio., 249, 303–308, https://doi.org/10.1098/rspb.1992.0119, 1992.
Hyodo, F., Tayasu, I., Inoue, T., Azuma, J. I., Kudo, T., and Abe, T.:
Differential role of symbiotic fungi in lignin degradation and food
provision for fungus-growing termites (Macrotermitinae: Isoptera),
Funct. Ecol., 17, 186–193, https://doi.org/10.1046/j.1365-2435.2003.00718.x,
2003.
Jamali, H., Livesley, S. J., Dawes, T. Z., Cook, G. D., Hutley, L. B., and
Arndt, S. K.: Diurnal and seasonal variations in CH4 flux from termite
mounds in tropical savannas of the Northern Territory, Australia,
Agr. Forest Meteorol., 151, 1471–1479,
https://doi.org/10.1016/j.agrformet.2010.06.009, 2011.
Jamali, H., Livesley, S. J., Hutley, L. B., Fest, B., and Arndt, S. K.: The relationships between termite mound emissions and internal concentration ratios are species specific, Biogeosciences, 10, 2229–2240, https://doi.org/10.5194/bg-10-2229-2013, 2013.
Jouquet, P., Traoré, S., Choosai, C., Hartmann, C., and Bignell, D.:
Influence of termites on ecosystem functioning. Ecosystem services provided
by termites, Europ. J. Soil Biol., 47, 215–222,
https://doi.org/10.1016/j.ejsobi.2011.05.005, 2011.
Khalil, M. A. K., Rasmussen, R. A., French, J. R. J., and Holt, J. A.: The
Influence of Termites on Atmospheric Trace Gases: CH4, CO2,
CHC13, N2O, CO, H2, and Light Hydrocarbons, J.
Geophys. Res.-Atmos., 95, 3619–3634, 1990.
King, H., Ocko, S., and Mahadevan, L.: Termite mounds harness diurnal
temperature oscillations for ventilation, P. Natl. Acad. Sci. USA,
112, 11589–11593, https://doi.org/10.1073/pnas.1423242112, 2015.
Kirschke, S., Bousquet, P., Ciais, P., Saunois, M., Canadell, J. G.
Dlugokencky, E. J. Bergamaschi, P. Bergmann, D., Blake, D. R., Bruhwiler,
L., Cameron-Smith, P., Castaldi, S., Chevallier, F., Feng, L., Fraser, A.,
Heimann, M., Hodson, E. L., Houweling, S., Josse, B., Fraser, P. J.,
Krummel, P. B., Lamarque, J. F. Langenfelds, R. L., Le Quere, C., Naik, V.,
O'Doherty, S., Palmer, P. I., Pison, I., Plummer, D., Poulter, B., Prinn, R.
G., Rigby, M., Ringeval, B., Santini, M., Schmidt, M., Shindell, D. T.,
Simpson, I. J., Spahni, R., Steele, L. P., Strode, S. A., Sudo, K., Szopa, S., van der Werf, G. R., Voulgarakis, A., van Weele, M., Weiss, R. F., Williams, J. E. and Zeng, G.: Three decades of global methane sources and sinks, Nat.
Geosci., 6, 813–823, https://doi.org/10.1038/ngeo1955, 2013.
Korb, J. and Linsenmair, K. E.: The effects of temperature on the
architecture and distribution of Macrotermes bellicosus (Isoptera,
Macrotermitinae) mounds in different habitats of a West African Guinea
savanna, Insectes Soc., 45, 51–65, https://doi.org/10.1007/s000400050068, 1998.
Korb, J.: Thermoregulation and ventilation of termite mounds,
Naturwissenschaften, 90, 212–219, https://doi.org/10.1007/s00114-002-0401-4, 2003.
Korb, J.: Termite Mound Architecture, from Function to Construction, in
Biology of Termites: A Modern Synthesis, edited by: Bignell, D. E., Roisin, Y.,
and Lo, N., Springer, Dordrecht, 349–373, 2011.
Lepage, M. G.: L'impact des populations récoltantes deMacrotermes
michaelseni (Sjöstedt) (Isoptera: Macrotermitinae) dans un
écosystème semi-aride (Kajiado-Kenya), I – L'activité de
récolte et son déterminisme, Insectes Soc., 28, 297–308, 1981a.
Lepage, M. G.: L'impact des populations récoltantes de Macrotermes
michaelseni (Sjöstedt) (Isoptera: Macrotermitinae) dans un
écosystème semi-aride (Kajiado-Kenya), II - La nourriture
récoltée, comparaison avec les grands herbivores, Insectes Soc.,
28, 309–319, 1981b.
Lepage, M., Abbadie, L., and Mariotti, A.: Food Habits of Sympatric Termite
Species (Isoptera, Macrotermitinae) as Determined by Stable Carbon Isotope
Analysis in a Guinean Savanna (Lamto, Cote d'Ivoire), J. Trop. Ecol., 3,
303–311, 1993.
Lüscher, M.: Air-Conditioned Termite Nests, Sci. Am., 205, 138–145,
https://doi.org/10.1038/scientificamerican0761-138, 1961.
Nauer, P. A., Hutley, L. B., and Arndt, S. K.: Termite mounds mitigate half
of termite methane emissions, P. Natl. Acad. Sci. USA, 115,
13306–13311, https://doi.org/10.1073/pnas.1809790115, 2018.
Noirot, C. and Darlington, J. P. E. C.: Termite nests: Architecture,
Regulation and Defence, in Termites: Evolution, Sociality, Symbioses,
Ecology, edited by: Abe, T., Bignell, D. E., and Higashi, M.,
Springer, 121–139, 2000.
Ocko, S. A., King, H., Andreen, D., Bardunias, P., Turner, J. S., Soar, R.
and Mahadevan, L.: Solar-powered ventilation of African termite mounds, J.
Exp. Biol., 220, 3260–3269, https://doi.org/10.1242/jeb.160895, 2017.
Pellikka, P. K. E., Heikinheimo, V., Hietanen, J., Schäfer, E.,
Siljander, M., and Heiskanen, J.: Impact of land cover change on aboveground
carbon stocks in Afromontane landscape in Kenya, Appl. Geogr., 94,
178–189, https://doi.org/10.1016/j.apgeog.2018.03.017, 2018.
Pomeroy, D. E.: Studies on a population of large termite mounds in Uganda,
Ecol. Entomol., 1, 49–61, https://doi.org/10.1111/j.1365-2311.1976.tb01204.x, 1976.
Pomeroy, D. E.: The Distribution and Abundance of Large Termite Mounds in
Uganda, J. Appl. Ecol., 14, 465–475, https://doi.org/10.2307/2402559, 1977.
Rouland-Lefèvre, C.: Symbiosis with fungi, in Termites: Evolution,
Sociality, Symbioses and Ecology, 289–306, 2000.
Räsänen, M., Merbold, L., Vakkari, V., Aurela, M., Laakso, L.,
Beukes, J. P., Zyl, P. G. V., Josipovic, M., Feig, G., Pellikka, P., Rinne,
J., and Katul, G. G.: Root-zone soil moisture variability across African
savannas: From pulsed rainfall to land-cover switches, Ecohydrology, 13,
e2213, https://doi.org/10.1002/eco.2213, 2020.
Räsänen, M., Vesala, R., Rönnholm, P., Arppe, L., Manninen, P.,
Jylhä, M., Rikkinen, J., Pellikka, P., and Rinne, J.: Dataset for
“Influence of termite mound structure and habitat on the mound CO2 and CH4
fluxes for fungus-growing termites”, figshare [data set],
https://doi.org/10.6084/m9.figshare.21739484.v1, 2022.
Sanderson, M. S.: Biomass of termites and their emissions of methane and
carbon dioxide: A global database, Global Biogeochem. Cy., 10,
543–557, https://doi.org/10.1029/96GB01893, 1996.
Sieber, R. and Leuthold, R. H.: Behavioural elements and their meaning in
incipient laboratory colonies of the fungus-growing Termite Macrotermes
michaelseni (Isoptera: Macrotermitinae), Insectes Soc., 28, 371–382,
https://doi.org/10.1007/BF02224194, 1981.
Sugimoto, A., Inoue, T., Kirtibutr, N., and Abe, T.: Methane oxidation by
termite mounds estimated by the carbon isotopic composition of methane,
Global Biogeochem. Cy., 12, 595–605, https://doi.org/10.1029/98GB02266, 1998.
Thomas, R. J.: Ecological studies on the symbiosis of Termitomyces Heim with
Nigerian Macrotermitinae, University of London, PhD Thesis, https://qmro.qmul.ac.uk/xmlui/handle/123456789/1777 (last access: 28 September 2023), 1981.
Wachiye, S., Merbold, L., Vesala, T., Rinne, J., Räsänen, M., Leitner, S., and Pellikka, P.: Soil greenhouse gas emissions under different land-use types in savanna ecosystems of Kenya, Biogeosciences, 17, 2149–2167, https://doi.org/10.5194/bg-17-2149-2020, 2020.
van Asperen, H., Alves-Oliveira, J. R., Warneke, T., Forsberg, B., de Araújo, A. C., and Notholt, J.: The role of termite CH4 emissions on the ecosystem scale: a case study in the Amazon rainforest, Biogeosciences, 18, 2609–2625, https://doi.org/10.5194/bg-18-2609-2021, 2021.
Vesala, R., Niskanen, T., Liimatainen, K., Boga, H., Pellikka, P., and
Rikkinen, J.: Diversity of fungus-growing termites (Macrotermes) and their
fungal symbionts (Termitomyces) in the semiarid Tsavo Ecosystem, Kenya,
Biotropica, 49, 402–412, https://doi.org/10.1111/btp.12422, 2017.
Vesala, R., Arppe, L., and Rikkinen, J.: Caste-specific nutritional
differences define carbon and nitrogen fluxes within symbiotic food webs in
African termite mounds, Sci. Rep., 9, 16611–16698,
https://doi.org/10.1038/s41598-019-53153-x, 2019a.
Vesala, R., Harjuntausta, A., Hakkarainen, A., Rönnholm, P., Pellikka,
P., and Rikkinen, J.: Termite mound architecture regulates nest temperature
and correlates with species identities of symbiotic fungi, Peer J., 6, e6237,
https://doi.org/10.7717/peerj.6237, 2019b.
Vesala, R., Arppe, L., and Rikkinen, J.: Termitomyces fungus combs –
formation, structure and functional aspects, in Microbial Symbionts:
Functions and Molecular Interactions on Host, edited by: Dhanasekaran, D.,
Academic Press., ISBN 9780323993340, 2022a.
Vesala, R., Rikkinen, A., Pellikka, P., Rikkinen, J., and Arppe, L.: You eat
what you find – local patterns in vegetation structure control diets of
African fungus-growing termites, Ecol. Evol., 12, e8566, https://doi.org/10.1002/ece3.8566, 2022b.
Virtanen, P., Gommers, R., Oliphant, T. E., Haberland, M., Reddy, T.,
Cournapeau, D., Burovski, E., Peterson, P., Weckesser, W., Bright, J., van
der Walt, S. J., Brett, M., Wilson, J., Millman, K. J., Mayorov, N., Nelson,
A. R. J., Jones, E., Kern, R., Larson, E., Carey, C. J., Polat, İ.,
Feng, Y., Moore, E. W., VanderPlas, J., Laxalde, D., Perktold, J., Cimrman,
R., Henriksen, I., Quintero, E. A., Harris, C. R., Archibald, A. M.,
Ribeiro, A. H., Pedregosa, F., van Mulbregt, P., and SciPy 1.0 Contributors:
SciPy 1.0: fundamental algorithms for scientific computing in Python, Nat.
Methods, 17, 261–272,
https://doi.org/10.1038/s41592-019-0686-2, 2020.
Weir, J. S.: Air Flow, Evaporation and Mineral Accumulation in Mounds of
Macrotermes subhyalinus (Rambur), J. Anim. Ecol., 42, 509–520,
https://doi.org/10.2307/3120, 1973.
Wildermuth, B., Oldeland, J., Arning, C., Gunter, F., Strohbach, B. and
Juergens, N.: Spatial patterns and life histories of Macrotermes michaelseni
termite mounds reflect intraspecific competition: Insights of a temporal
comparison spanning 12 years, Ecography, 9, e06306, https://doi.org/10.1111/ecog.06306, 2022.
Wood, T. G. and Thomas, R. J.: The mutualistic association between
Macrotermitinae and Termitomyces, in: Insect-fungus interactions, edited by:
Wilding, N., Collins, N. M., Hammond, P. M., and Webber, J. F., Academic Press., 69–92,
1989.
Zhou, Y., Staver, A. C., and Davies, A. B.: Species-level termite methane
production rates, Ecology, 104, e3905, https://doi.org/10.1002/ecy.3905,
2023.
Zimmerman, P. R., Greenberg, J. P., Wandiga, S. O., and Crutzen, P. J.:
Termites: A Potentially Large Source of Atmospheric Methane, Carbon Dioxide,
and Molecular Hydrogen, Science, 218, 563–565, 1982.
Short summary
Fungus-growing termites recycle large parts of dead plant material in African savannas and are significant sources of greenhouse gases. We measured CO2 and CH4 fluxes from their mounds and surrounding soils in open and closed habitats. The fluxes scale with mound volume. The results show that emissions from mounds of fungus-growing termites are more stable than those from other termites. The soil fluxes around the mound are affected by the termite colonies at up to 2 m distance from the mound.
Fungus-growing termites recycle large parts of dead plant material in African savannas and are...
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