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A Role for Parasites in Stabilising the Fig-Pollinator Mutualism
Mutualisms are interspecific interactions in which both players benefit. Explaining their maintenance is problematic, because cheaters should outcompete cooperative conspecifics, leading to mutualism instability. Monoecious figs (Ficus) are pollinated by host-specific wasps (Agaonidae), whose larvae...
Autores principales: | , , , , , , |
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Formato: | Texto |
Lenguaje: | English |
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Public Library of Science
2008
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2265770/ https://www.ncbi.nlm.nih.gov/pubmed/18336072 http://dx.doi.org/10.1371/journal.pbio.0060059 |
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author | Dunn, Derek W Segar, Simon T Ridley, Jo Chan, Ruth Crozier, Ross H Yu, Douglas W Cook, James M |
author_facet | Dunn, Derek W Segar, Simon T Ridley, Jo Chan, Ruth Crozier, Ross H Yu, Douglas W Cook, James M |
author_sort | Dunn, Derek W |
collection | PubMed |
description | Mutualisms are interspecific interactions in which both players benefit. Explaining their maintenance is problematic, because cheaters should outcompete cooperative conspecifics, leading to mutualism instability. Monoecious figs (Ficus) are pollinated by host-specific wasps (Agaonidae), whose larvae gall ovules in their “fruits” (syconia). Female pollinating wasps oviposit directly into Ficus ovules from inside the receptive syconium. Across Ficus species, there is a widely documented segregation of pollinator galls in inner ovules and seeds in outer ovules. This pattern suggests that wasps avoid, or are prevented from ovipositing into, outer ovules, and this results in mutualism stability. However, the mechanisms preventing wasps from exploiting outer ovules remain unknown. We report that in Ficus rubiginosa, offspring in outer ovules are vulnerable to attack by parasitic wasps that oviposit from outside the syconium. Parasitism risk decreases towards the centre of the syconium, where inner ovules provide enemy-free space for pollinator offspring. We suggest that the resulting gradient in offspring viability is likely to contribute to selection on pollinators to avoid outer ovules, and by forcing wasps to focus on a subset of ovules, reduces their galling rates. This previously unidentified mechanism may therefore contribute to mutualism persistence independent of additional factors that invoke plant defences against pollinator oviposition, or physiological constraints on pollinators that prevent oviposition in all available ovules. |
format | Text |
id | pubmed-2265770 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2008 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-22657702008-03-11 A Role for Parasites in Stabilising the Fig-Pollinator Mutualism Dunn, Derek W Segar, Simon T Ridley, Jo Chan, Ruth Crozier, Ross H Yu, Douglas W Cook, James M PLoS Biol Research Article Mutualisms are interspecific interactions in which both players benefit. Explaining their maintenance is problematic, because cheaters should outcompete cooperative conspecifics, leading to mutualism instability. Monoecious figs (Ficus) are pollinated by host-specific wasps (Agaonidae), whose larvae gall ovules in their “fruits” (syconia). Female pollinating wasps oviposit directly into Ficus ovules from inside the receptive syconium. Across Ficus species, there is a widely documented segregation of pollinator galls in inner ovules and seeds in outer ovules. This pattern suggests that wasps avoid, or are prevented from ovipositing into, outer ovules, and this results in mutualism stability. However, the mechanisms preventing wasps from exploiting outer ovules remain unknown. We report that in Ficus rubiginosa, offspring in outer ovules are vulnerable to attack by parasitic wasps that oviposit from outside the syconium. Parasitism risk decreases towards the centre of the syconium, where inner ovules provide enemy-free space for pollinator offspring. We suggest that the resulting gradient in offspring viability is likely to contribute to selection on pollinators to avoid outer ovules, and by forcing wasps to focus on a subset of ovules, reduces their galling rates. This previously unidentified mechanism may therefore contribute to mutualism persistence independent of additional factors that invoke plant defences against pollinator oviposition, or physiological constraints on pollinators that prevent oviposition in all available ovules. Public Library of Science 2008-03 2008-03-11 /pmc/articles/PMC2265770/ /pubmed/18336072 http://dx.doi.org/10.1371/journal.pbio.0060059 Text en © 2008 Dunn et al. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited. |
spellingShingle | Research Article Dunn, Derek W Segar, Simon T Ridley, Jo Chan, Ruth Crozier, Ross H Yu, Douglas W Cook, James M A Role for Parasites in Stabilising the Fig-Pollinator Mutualism |
title | A Role for Parasites in Stabilising the Fig-Pollinator Mutualism |
title_full | A Role for Parasites in Stabilising the Fig-Pollinator Mutualism |
title_fullStr | A Role for Parasites in Stabilising the Fig-Pollinator Mutualism |
title_full_unstemmed | A Role for Parasites in Stabilising the Fig-Pollinator Mutualism |
title_short | A Role for Parasites in Stabilising the Fig-Pollinator Mutualism |
title_sort | role for parasites in stabilising the fig-pollinator mutualism |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2265770/ https://www.ncbi.nlm.nih.gov/pubmed/18336072 http://dx.doi.org/10.1371/journal.pbio.0060059 |
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