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...

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Main Authors: Derek W Dunn, Simon T Segar, Jo Ridley, Ruth Chan, Ross H Crozier, Douglas W Yu, James M Cook
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2008-03-01
Series:PLoS Biology
Online Access:https://www.ncbi.nlm.nih.gov/pmc/articles/pmid/18336072/?tool=EBI
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spelling doaj-3b715868ba0540c69319519069373f142021-07-02T17:09:05ZengPublic Library of Science (PLoS)PLoS Biology1544-91731545-78852008-03-0163e5910.1371/journal.pbio.0060059A role for parasites in stabilising the fig-pollinator mutualism.Derek W DunnSimon T SegarJo RidleyRuth ChanRoss H CrozierDouglas W YuJames M CookMutualisms 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.https://www.ncbi.nlm.nih.gov/pmc/articles/pmid/18336072/?tool=EBI
collection DOAJ
language English
format Article
sources DOAJ
author Derek W Dunn
Simon T Segar
Jo Ridley
Ruth Chan
Ross H Crozier
Douglas W Yu
James M Cook
spellingShingle Derek W Dunn
Simon T Segar
Jo Ridley
Ruth Chan
Ross H Crozier
Douglas W Yu
James M Cook
A role for parasites in stabilising the fig-pollinator mutualism.
PLoS Biology
author_facet Derek W Dunn
Simon T Segar
Jo Ridley
Ruth Chan
Ross H Crozier
Douglas W Yu
James M Cook
author_sort Derek W Dunn
title A role for parasites in stabilising the fig-pollinator mutualism.
title_short 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_sort role for parasites in stabilising the fig-pollinator mutualism.
publisher Public Library of Science (PLoS)
series PLoS Biology
issn 1544-9173
1545-7885
publishDate 2008-03-01
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.
url https://www.ncbi.nlm.nih.gov/pmc/articles/pmid/18336072/?tool=EBI
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