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Trophic position, elemental ratios and nitrogen transfer in a planktonic host–parasite–consumer food chain including a fungal parasite
Parasitism is arguably the most commonly occurring consumer strategy. However, only a few food web studies assess how well stable isotopes reflect the trophic position of parasitic consumers and results are variable. Even fewer studies have measured the nutrient transfer by parasitic consumers, hind...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer Berlin Heidelberg
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7683484/ https://www.ncbi.nlm.nih.gov/pubmed/32803339 http://dx.doi.org/10.1007/s00442-020-04721-w |
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author | Sánchez Barranco, Virginia Van der Meer, Marcel T. J. Kagami, Maiko Van den Wyngaert, Silke Van de Waal, Dedmer B. Van Donk, Ellen Gsell, Alena S. |
author_facet | Sánchez Barranco, Virginia Van der Meer, Marcel T. J. Kagami, Maiko Van den Wyngaert, Silke Van de Waal, Dedmer B. Van Donk, Ellen Gsell, Alena S. |
author_sort | Sánchez Barranco, Virginia |
collection | PubMed |
description | Parasitism is arguably the most commonly occurring consumer strategy. However, only a few food web studies assess how well stable isotopes reflect the trophic position of parasitic consumers and results are variable. Even fewer studies have measured the nutrient transfer by parasitic consumers, hindering an assessment of their role in nutrient transfer through food webs. Here we used a food chain consisting of a diatom as host, a chytrid as its parasitic consumer and a rotifer as the predatory consumer of the chytrid, to assess the trophic position of all three food-chain components using their natural (13)C and (15)N isotope signatures, and to measure the nitrogen transfer from the host via the chytrid to the rotifer by tracing (15)N of a labelled host up the food chain. Additionally, we measured the carbon to nitrogen (C:N) ratios of all food-chain components. Natural isotope abundance results showed no clear (15)N enrichment in the chytrid or rotifer relative to the primary producer. However, estimates of nitrogen transfer indicated that about 14% of host nitrogen was transferred per day from host to chytrid during infection epidemics and that some of this nitrogen was also transferred onward to the rotifer. Moreover, C:N ratios decreased with trophic level, suggesting that the chytrid provided a high-quality food source to the rotifer. In conclusion, our results support the “mycoloop”. The mycooloop proposes that chytrid infections allow the transfer of nutrients bound in large, inedible phytoplankton to zooplankton through the production of edible transmission spores, thereby rerouting nutrients back into the food web. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1007/s00442-020-04721-w) contains supplementary material, which is available to authorized users. |
format | Online Article Text |
id | pubmed-7683484 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Springer Berlin Heidelberg |
record_format | MEDLINE/PubMed |
spelling | pubmed-76834842020-11-30 Trophic position, elemental ratios and nitrogen transfer in a planktonic host–parasite–consumer food chain including a fungal parasite Sánchez Barranco, Virginia Van der Meer, Marcel T. J. Kagami, Maiko Van den Wyngaert, Silke Van de Waal, Dedmer B. Van Donk, Ellen Gsell, Alena S. Oecologia Highlighted Student Research Parasitism is arguably the most commonly occurring consumer strategy. However, only a few food web studies assess how well stable isotopes reflect the trophic position of parasitic consumers and results are variable. Even fewer studies have measured the nutrient transfer by parasitic consumers, hindering an assessment of their role in nutrient transfer through food webs. Here we used a food chain consisting of a diatom as host, a chytrid as its parasitic consumer and a rotifer as the predatory consumer of the chytrid, to assess the trophic position of all three food-chain components using their natural (13)C and (15)N isotope signatures, and to measure the nitrogen transfer from the host via the chytrid to the rotifer by tracing (15)N of a labelled host up the food chain. Additionally, we measured the carbon to nitrogen (C:N) ratios of all food-chain components. Natural isotope abundance results showed no clear (15)N enrichment in the chytrid or rotifer relative to the primary producer. However, estimates of nitrogen transfer indicated that about 14% of host nitrogen was transferred per day from host to chytrid during infection epidemics and that some of this nitrogen was also transferred onward to the rotifer. Moreover, C:N ratios decreased with trophic level, suggesting that the chytrid provided a high-quality food source to the rotifer. In conclusion, our results support the “mycoloop”. The mycooloop proposes that chytrid infections allow the transfer of nutrients bound in large, inedible phytoplankton to zooplankton through the production of edible transmission spores, thereby rerouting nutrients back into the food web. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1007/s00442-020-04721-w) contains supplementary material, which is available to authorized users. Springer Berlin Heidelberg 2020-08-17 2020 /pmc/articles/PMC7683484/ /pubmed/32803339 http://dx.doi.org/10.1007/s00442-020-04721-w Text en © The Author(s) 2020 Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Highlighted Student Research Sánchez Barranco, Virginia Van der Meer, Marcel T. J. Kagami, Maiko Van den Wyngaert, Silke Van de Waal, Dedmer B. Van Donk, Ellen Gsell, Alena S. Trophic position, elemental ratios and nitrogen transfer in a planktonic host–parasite–consumer food chain including a fungal parasite |
title | Trophic position, elemental ratios and nitrogen transfer in a planktonic host–parasite–consumer food chain including a fungal parasite |
title_full | Trophic position, elemental ratios and nitrogen transfer in a planktonic host–parasite–consumer food chain including a fungal parasite |
title_fullStr | Trophic position, elemental ratios and nitrogen transfer in a planktonic host–parasite–consumer food chain including a fungal parasite |
title_full_unstemmed | Trophic position, elemental ratios and nitrogen transfer in a planktonic host–parasite–consumer food chain including a fungal parasite |
title_short | Trophic position, elemental ratios and nitrogen transfer in a planktonic host–parasite–consumer food chain including a fungal parasite |
title_sort | trophic position, elemental ratios and nitrogen transfer in a planktonic host–parasite–consumer food chain including a fungal parasite |
topic | Highlighted Student Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7683484/ https://www.ncbi.nlm.nih.gov/pubmed/32803339 http://dx.doi.org/10.1007/s00442-020-04721-w |
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