Literature DB >> 30836880

Parasite-offspring competition for female resources can explain male-biased parasitism in plants.

Kirsty J Yule1, Kevin C Burns1.   

Abstract

Male-biased susceptibility to parasites is common in dioecious plants. However, why males have higher parasite loads than females is unclear. Unlike males, females must subsidize post-fertilization costs of reproduction (e.g. seed and fruit development). As a result, females may have smaller pools of resources potentially available to parasites, thus leading to lower parasite loads. We tested this prediction in New Zealand's largest native moth ( Aenetus virescens: Lepidoptera), whose larvae parasitize Aristotelia serrata (Elaeocarpaceae), an endemic species of dioecious tree. We measured parasite loads in male and female trees, as well as annual seed set in females. We then derived a technique to equate the energetic cost of seed set in females to an equivalent number of parasitic larvae. Our results showed evidence for male-biased parasitism: male trees harboured more larval parasites than female trees. However, when parasite loads in males were compared with parasite loads in females, plus the energetic cost of seed production calculated as an equivalent number of parasitic larvae, differences in parasitism between the sexes disappeared. We conclude that male-biased parasitism in plants could arise from parasite-offspring (i.e. herbivore-seed) competition for female resources.

Entities:  

Keywords:  dioecy; gender; herbivory; reproduction; sexual dimorphism

Mesh:

Year:  2019        PMID: 30836880      PMCID: PMC6451378          DOI: 10.1098/rsbl.2018.0761

Source DB:  PubMed          Journal:  Biol Lett        ISSN: 1744-9561            Impact factor:   3.703


  10 in total

1.  Allometry of sexual size dimorphism in dioecious plants: do plants obey Rensch's rule?

Authors:  P H Kavanagh; C A Lehnebach; M J Shea; K C Burns
Journal:  Am Nat       Date:  2011-10-06       Impact factor: 3.926

2.  Reversal of height dimorphism promotes pollen and seed dispersal in a wind-pollinated dioecious plant.

Authors:  Melinda Pickup; Spencer C H Barrett
Journal:  Biol Lett       Date:  2011-11-02       Impact factor: 3.703

3.  Sex-related differences in stress tolerance in dioecious plants: a critical appraisal in a physiological context.

Authors:  Marta Juvany; Sergi Munné-Bosch
Journal:  J Exp Bot       Date:  2015-07-10       Impact factor: 6.992

4.  Adaptive advantages of appearance: predation, thermoregulation, and color of webbing built by New Zealand's largest moth.

Authors:  Kirsty Yule; Kevin Burns
Journal:  Ecology       Date:  2017-04-07       Impact factor: 5.499

5.  NIH Image to ImageJ: 25 years of image analysis.

Authors:  Caroline A Schneider; Wayne S Rasband; Kevin W Eliceiri
Journal:  Nat Methods       Date:  2012-07       Impact factor: 28.547

6.  Drivers of aggregation in a novel arboreal parasite: the influence of host size and infra-populations.

Authors:  Kirsty J Yule; Kevin C Burns
Journal:  Int J Parasitol       Date:  2014-12-20       Impact factor: 3.981

7.  Dividing a Maternal Pie among Half-Sibs: Genetic Conflicts and the Control of Resource Allocation to Seeds in Maize.

Authors:  Aurélie Cailleau; Daniel Grimanelli; Elodie Blanchet; Pierre-Olivier Cheptou; Thomas Lenormand
Journal:  Am Nat       Date:  2018-09-12       Impact factor: 3.926

Review 8.  Sexual dimorphism in flowering plants.

Authors:  Spencer C H Barrett; Josh Hough
Journal:  J Exp Bot       Date:  2012-11-25       Impact factor: 6.992

Review 9.  Hormonal and immunological mechanisms mediating sex differences in parasite infection.

Authors:  S L Klein
Journal:  Parasite Immunol       Date:  2004 Jun-Jul       Impact factor: 2.280

10.  The evolution of sex-specific virulence in infectious diseases.

Authors:  Francisco Úbeda; Vincent A A Jansen
Journal:  Nat Commun       Date:  2016-12-13       Impact factor: 14.919

  10 in total

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