Literature DB >> 15119439

Codiversification in an ant-plant mutualism: stem texture and the evolution of host use in Crematogaster (Formicidae: Myrmicinae) inhabitants of Macaranga (Euphorbiaceae).

Swee-Peck Quek1, Stuart J Davies, Takao Itino, Naomi E Pierce.   

Abstract

We investigate the evolution of host association in a cryptic complex of mutualistic Crematogaster (Decacrema) ants that inhabits and defends Macaranga trees in Southeast Asia. Previous phylogenetic studies based on limited samplings of Decacrema present conflicting reconstructions of the evolutionary history of the association, inferring both cospeciation and the predominance of host shifts. We use cytochrome oxidase I (COI) to reconstruct phylogenetic relationships in a comprehensive sampling of the Decacrema inhabitants of Macaranga. Using a published Macaranga phylogeny, we test whether the ants and plants have cospeciated. The COI phylogeny reveals 10 well-supported lineages and an absence of cospeciation. Host shifts, however, have been constrained by stem traits that are themselves correlated with Macaranga phylogeny. Earlier lineages of Decacrema exclusively inhabit waxy stems, a basal state in the Pachystemon clade within Macaranga, whereas younger species of Pachystemon, characterized by nonwaxy stems, are inhabited only by younger lineages of Decacrema. Despite the absence of cospeciation, the correlated succession of stem texture in both phylogenies suggests that Decacrema and Pachystemon have diversified in association, or codiversified. Subsequent to the colonization of the Pachystemon clade, Decacrema expanded onto a second clade within Macaranga, inducing the development of myrmecophytism in the Pruinosae group. Confinement to the aseasonal wet climate zone of western Malesia suggests myrmecophytic Macaranga are no older than the wet forest community in Southeast Asia, estimated to be about 20 million years old (early Miocene). Our calculation of COI divergence rates from several published arthropod studies that relied on tenable calibrations indicates a generally conserved rate of approximately 1.5% per million years. Applying this rate to a rate-smoothed Bayesian chronogram of the ants, the Decacrema from Macaranga are inferred to be at least 12 million years old (mid-Miocene). However, using the extremes of rate variation in COI produces an age as recent as 6 million years. Our inferred timeline based on 1.5% per million years concurs with independent biogeographical events in the region reconstructed from palynological data, thus suggesting that the evolutionary histories of Decacrema and their Pachystemon hosts have been contemporaneous since the mid-Miocene. The evolution of myrmecophytism enabled Macaranga to radiate into enemy-free space, while the ants' diversification has been shaped by stem traits, host specialization, and geographic factors. We discuss the possibility that the ancient and exclusive association between Decacrema and Macaranga was facilitated by an impoverished diversity of myrmecophytes and phytoecious (obligately plant inhabiting) ants in the region.

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Year:  2004        PMID: 15119439

Source DB:  PubMed          Journal:  Evolution        ISSN: 0014-3820            Impact factor:   3.694


  41 in total

1.  Macroevolutionary assembly of ant/plant symbioses: Pseudomyrmex ants and their ant-housing plants in the Neotropics.

Authors:  Guillaume Chomicki; Philip S Ward; Susanne S Renner
Journal:  Proc Biol Sci       Date:  2015-11-22       Impact factor: 5.349

2.  Repeated independent evolution of obligate pollination mutualism in the Phyllantheae-Epicephala association.

Authors:  Atsushi Kawakita; Makoto Kato
Journal:  Proc Biol Sci       Date:  2009-02-07       Impact factor: 5.349

3.  Population genetics of ecological communities with DNA barcodes: an example from New Guinea Lepidoptera.

Authors:  Kathleen J Craft; Steffen U Pauls; Karolyn Darrow; Scott E Miller; Paul D N Hebert; Lauren E Helgen; Vojtech Novotny; George D Weiblen
Journal:  Proc Natl Acad Sci U S A       Date:  2010-03-02       Impact factor: 11.205

4.  Homoploid hybrid speciation and genome evolution via chromosome sorting.

Authors:  Vladimir A Lukhtanov; Nazar A Shapoval; Boris A Anokhin; Alsu F Saifitdinova; Valentina G Kuznetsova
Journal:  Proc Biol Sci       Date:  2015-05-22       Impact factor: 5.349

5.  Unexpected layers of cryptic diversity in wood white Leptidea butterflies.

Authors:  Vlad Dincă; Vladimir A Lukhtanov; Gerard Talavera; Roger Vila
Journal:  Nat Commun       Date:  2011       Impact factor: 14.919

6.  Phylogenetic analysis of European Scutovertex mites (Acari, Oribatida, Scutoverticidae) reveals paraphyly and cryptic diversity: A molecular genetic and morphological approach.

Authors:  Sylvia Schäffer; Tobias Pfingstl; Stephan Koblmüller; Kathrin A Winkler; Christian Sturmbauer; Günther Krisper
Journal:  Mol Phylogenet Evol       Date:  2009-12-16       Impact factor: 4.286

7.  Cryptic genetic and wing pattern diversity in a mimetic Heliconius butterfly.

Authors:  R I Hill; L E Gilbert; M R Kronforst
Journal:  Mol Ecol       Date:  2013-03-26       Impact factor: 6.185

8.  Evolutionary diversification of cryophilic Grylloblatta species (Grylloblattodea: Grylloblattidae) in alpine habitats of California.

Authors:  Sean D Schoville; George K Roderick
Journal:  BMC Evol Biol       Date:  2010-06-02       Impact factor: 3.260

9.  When environmental changes do not cause geographic separation of fauna: differential responses of Baikalian invertebrates.

Authors:  Varvara Fazalova; Bruno Nevado; Tatiana Peretolchina; Jeanna Petunina; Dmitry Sherbakov
Journal:  BMC Evol Biol       Date:  2010-10-23       Impact factor: 3.260

10.  Mitochondrial DNA indicates late pleistocene divergence of populations of Heteronympha merope, an emerging model in environmental change biology.

Authors:  Melanie Norgate; Jay Chamings; Alexandra Pavlova; James K Bull; Neil D Murray; Paul Sunnucks
Journal:  PLoS One       Date:  2009-11-24       Impact factor: 3.240

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