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Oxygen dynamics and transport in the Mediterranean sponge Aplysina aerophoba
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The Mediterranean sponge Aplysina aerophoba kept in aquaria or cultivation tanks can stop pumping for several hours or even days. To investigate changes in the chemical microenvironments, we measured oxygen profiles over the surface and into the tissue of pumping and non-pumping A. aerophoba specimens with Clark-type oxygen microelectrodes (tip diameters 18–30 μm). Total oxygen consumption rates of whole sponges were measured in closed chambers. These rates were used to back-calculate the oxygen distribution in a finite-element model. Combining direct measurements with calculations of diffusive flux and modeling revealed that the tissue of non-pumping sponges turns anoxic within 15 min, with the exception of a 1 mm surface layer where oxygen intrudes due to molecular diffusion over the sponge surface. Molecular diffusion is the only transport mechanism for oxygen into non-pumping sponges, which allows total oxygen consumption rates of 6–12 μmol cm −3 sponge day −1 . Sponges of different sizes had similar diffusional uptake rates, which is explained by their similar surface/volume ratios. In pumping sponges, oxygen consumption rates were between 22 and 37 μmol cm −3 sponge day −1 , and the entire tissue was oxygenated. Combining different approaches of direct oxygen measurement in living sponges with a dynamic model, we can show that tissue anoxia is a direct function of the pumping behavior. The sponge-microbe system of A. aerophoba thus has the possibility to switch actively between aerobic and anaerobic metabolism by stopping the water flow for more than 15 min. These periods of anoxia will greatly influence physiological variety and activity of the sponge microbes. Detailed knowledge about the varying chemical microenvironments in sponges will help to develop protocols to cultivate sponge-associated microbial lineages and improve our understanding of the sponge-microbe-system.
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“Internal anoxia, however, does appear to be a common feature of sponge physiology (34,35).”
From Oxygen requirements of the earliest animals (2014) · cites this paper as [35]
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Cites
Diffusion of ions in sea water and in deep-sea sediments
Yuan-Hui, L., & Gregory, S. (1974) · Geochimica et Cosmochimica Acta · doi:10.1016/0016-7037(74)90145-8 · Cited by 2,875
Sponge-Associated Microorganisms: Evolution, Ecology, and Biotechnological Potential
Taylor, M. W., Radax, R., Steger, D., & Wagner, M. (2007) · Microbiology and Molecular Biology Reviews · doi:10.1128/mmbr.00040-06 · Cited by 1,493
An oxygen microsensor with a guard cathode
Revsbech, N. P. (1989) · Limnology and Oceanography · doi:10.4319/lo.1989.34.2.0474 · Cited by 1,133
Continuous Recording of Blood Oxygen Tensions by Polarography
Clark, L. C., Wolf, R., Granger, D., & Taylor, Z. (1953) · Journal of Applied Physiology · doi:10.1152/jappl.1953.6.3.189 · Cited by 885
Diffusive boundary layers and the oxygen uptake of sediments and detritus1
Jørgensen, B. B., & Revsbech, N. P. (1985) · Limnology and Oceanography · doi:10.4319/lo.1985.30.1.0111 · Cited by 791
Molecular Evidence for a Uniform Microbial Community in Sponges from Different Oceans
Hentschel, U., Hopke, J. N., Horn, M., Friedrich, A. B., Wagner, M., Hacker, J. H., & Moore, B. S. (2002) · Applied and Environmental Microbiology · doi:10.1128/aem.68.9.4431-4440.2002 · Cited by 703
Self-citationMicroelectrode studies of seasonal oxygen uptake in a coastal sediment: role of molecular diffusion
Rasmussen, H., & Jørgensen, B. B. (1992) · Marine Ecology Progress Series · doi:10.3354/meps081289 · Cited by 380
Water transport, respiration and energetics of three tropical marine sponges
Reiswig, H. M. (1974) · Journal of Experimental Marine Biology and Ecology · doi:10.1016/0022-0981(74)90005-7 · Cited by 378
In situ pumping activities of tropical Demospongiae
Reiswig, H. M. (1971) · Marine Biology · doi:10.1007/bf00348816 · Cited by 308
Current-induced flow through living sponges in nature.
Vogel, S. K. (1977) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.74.5.2069 · Cited by 276
Research works printed but not linked: 1
- Vacelet J (1975) Étude en microscopiie électronique de l’association entre bactéries et spongiaires du genre Verongia (Dyctioceratida). J Micros Biol Cell 23:271–288
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Fan, L., Reynolds, D., Liu, M., Stark, M., Kjelleberg, S. J., Webster, N. S., & Thomas, T. (2012) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1203287109 · Cited by 401
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Self-citationSiegl, A., Kamke, J., Hochmuth, T., Piel, J., Richter, M., Liang, C., Dandekar, T., & Hentschel, U. (2011) · The ISME Journal · doi:10.1038/ismej.2010.95 · Cited by 276
Self-citationStief, P. (2013) · Biogeosciences · doi:10.5194/bg-10-7829-2013 · Cited by 185
Bayer, K., Schmitt, S., & Hentschel, U. (2008) · Environmental Microbiology · doi:10.1111/j.1462-2920.2008.01582.x · Cited by 166
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Schläppy, M., Schöttner, S., Lavik, G., Kuypers, M. M. M., de Beer, D., & Hoffmann, F. (2009) · Marine Biology · doi:10.1007/s00227-009-1344-5 · Cited by 157
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Riesgo, A., Santodomingo, N., Koutsouveli, V., Kumala, L., Leger, M. M., Leys, S. P., & Funch, P. (2024) · Figshare · doi:10.6084/m9.figshare.26558066
Riesgo, A., Santodomingo, N., Koutsouveli, V., Kumala, L., Leger, M. M., Leys, S. P., & Funch, P. (2024) · Figshare · doi:10.6084/m9.figshare.26558054
Riesgo, A., Santodomingo, N., Koutsouveli, V., Kumala, L., Leger, M. M., Leys, S. P., & Funch, P. (2024) · Figshare · doi:10.6084/m9.figshare.26558063
Riesgo, A., Santodomingo, N., Koutsouveli, V., Kumala, L., Leger, M. M., Leys, S. P., & Funch, P. (2024) · Figshare · doi:10.6084/m9.figshare.26558051
Metadata
- Authors
- Hoffmann, F., Røy, H., Bayer, K., Hentschel, U., Pfannkuchen, M., Brümmer, F., & de Beer, D.
- Affiliations
- Max Planck Institute for Marine Microbiology (DE)
- Aarhus University (DK)
- University of Würzburg (DE)
- University of Stuttgart (DE)
- Corresponding author
- Hoffmann, Friederike
- Venue
- Marine Biology
- Published
- 2008-01-22
- Volume
- 153
- Issue
- 6
- Pages
- 1257-1264
- ISSN
- 0025-3162 (ISSN-L)
- 1432-1793
- PMC
- PMC3873076
- OpenAlex
- W2112561701
- Cited by
- 107
- References
- 24
- Citations by year
- 2026: 6 · 2025: 3 · 2024: 13 · 2023: 5 · 2022: 10 · 2021: 9 · 2020: 5 · 2019: 5 · 2018: 6 · 2017: 4 · 2016: 5 · 2015: 5 · 2014: 4 · 2013: 4 · 2012: 4
- FWCI
- 5.20
- Type
- journal article
- Language
- en
- Open access
- hybrid
- doi.org
- Licence
- Locations
- Marine Biology (publishedVersion, cc-by-nc)
- Europe PMC (PubMed Central) (publishedVersion)
- PubMed Central (publishedVersion)
- PubMed (publishedVersion)
- Helmholtz Centre for Ocean Research Kiel (GEOMAR) (submittedVersion)
- MPG.PuRe (Max Planck Society) (submittedVersion, other-oa)
- Max Planck Digital Library (submittedVersion)
- Funders
- Deutsche Forschungsgemeinschaft
- Bundesministerium für Bildung und Forschung
- Topics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Biotechnology › Marine Sponges and Natural Products
- Life Sciences › Agricultural and Biological Sciences › Animal Science and Zoology › Marine Invertebrate Physiology and Ecology
- Physical Sciences › Environmental Science › Ecology › Physiological and biochemical adaptations
- Keywords
- Aplysina aerophoba, oxygen transport, tissue anoxia, oxygen consumption rate, molecular diffusion, finite element model, aerobic and anaerobic metabolism, chemical microenvironment
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