Literature DB >> 27194059

Differential Recruitment of Camponotus femoratus (Fabricius) Ants in Response to Ant Garden Herbivory.

R E Vicente1, W Dáttilo2, T J Izzo3.   

Abstract

Although several studies have shown that ants can recognize chemical cues from their host plants in ant-plant systems, it is poorly demonstrated in ant gardens (AGs). In this interaction, ant species constantly interact with various epiphyte species. Therefore, it is possible to expect a convergence of chemical signals released by plants that could be acting to ensure that ants are able to recognize and defend epiphyte species frequently associated with AGs. In this study, it was hypothesized that ants recognize and differentiate among chemical stimuli released by AG epiphytes and non-AG epiphytes. We experimentally simulated leaf herbivore damage on three epiphyte species restricted to AGs and a locally abundant understory herb, Piper hispidum, in order to quantify the number of recruited Camponotus femoratus (Fabricius) defenders. When exposed to the AG epiphytes Peperomia macrostachya and Codonanthe uleana leaves, it was observed that the recruitment of C. femoratus workers was, on average, respectively 556% and 246% higher than control. However, the number of ants recruited by the AG epiphyte Markea longiflora or by the non-AG plant did not differ from paper pieces. This indicated that ants could discern between chemicals released by different plants, suggesting that ants can select better plants. These results can be explained by evolutionary process acting on both ants' capability in discerning plants' chemical compounds (innate attraction) or by ants' learning based on the epiphyte frequency in AGs (individual experience). To disentangle an innate behavior, a product of classical coevolutionary process, from an ant's learned behavior, is a complicated but important subject to understand in the evolution of ant-plant mutualisms.

Entities:  

Keywords:  Ant-gardens; Codonanthe uleana; Peperomia macrostachya; ant-plant system; herbivory; mutualism

Mesh:

Year:  2014        PMID: 27194059     DOI: 10.1007/s13744-014-0245-6

Source DB:  PubMed          Journal:  Neotrop Entomol        ISSN: 1519-566X            Impact factor:   1.434


  12 in total

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3.  Pursuing the big questions about interspecific mutualism: a review of theoretical approaches.

Authors:  Jason D Hoeksema; Emilio M Bruna
Journal:  Oecologia       Date:  2000-11-01       Impact factor: 3.225

4.  Species diversity and distribution patterns of the ants of Amazonian Ecuador.

Authors:  Kari T Ryder Wilkie; Amy L Mertl; James F A Traniello
Journal:  PLoS One       Date:  2010-10-01       Impact factor: 3.240

5.  For ant-protected plants, the best defense is a hungry offense.

Authors:  J H Ness; W F Morris; Judith L Bronstein
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6.  Seed odor mediates an obligate ant-plant mutualism in Amazonian rainforests.

Authors:  Elsa Youngsteadt; Satoshi Nojima; Christopher Häberlein; Stefan Schulz; Coby Schal
Journal:  Proc Natl Acad Sci U S A       Date:  2008-01-22       Impact factor: 11.205

7.  Innate attraction supplants experience during host plant selection in an obligate plant-ant.

Authors:  C Djieto-Lordon; A Dejean
Journal:  Behav Processes       Date:  1999-07       Impact factor: 1.777

8.  Experience influences aggressive behaviour in the Argentine ant.

Authors:  Ellen Van Wilgenburg; Johanna Clémencet; Neil D Tsutsui
Journal:  Biol Lett       Date:  2009-09-30       Impact factor: 3.703

9.  Divergent chemical cues elicit seed collecting by ants in an obligate multi-species mutualism in lowland Amazonia.

Authors:  Elsa Youngsteadt; Patricia Guerra Bustios; Coby Schal
Journal:  PLoS One       Date:  2010-12-30       Impact factor: 3.240

10.  Role of early experience in ant enslavement: a comparative analysis of a host and a non-host species.

Authors:  Rumsaïs Blatrix; Claire Sermage
Journal:  Front Zool       Date:  2005-08-02       Impact factor: 3.172

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