Literature DB >> 14653784

Unexpected patterns of genetic structuring among locations but not colour morphs in Acropora nasuta (Cnidaria; Scleractinia).

J B Mackenzie1, P L Munday, B L Willis, D J Miller, M J H van Oppen.   

Abstract

Symbiotic relationships have contributed greatly to the evolution and maintenance of biological diversity. On the Great Barrier Reef, species of obligate coral-dwelling fishes (genus Gobiodon) coexist by selectively recruiting to colonies of Acropora nasuta that differ in branch-tip colour. In this study, we investigate genetic variability among sympatric populations of two colour morphs of A. nasuta ('blue-tip' and 'brown-tip') living in symbiosis with two fish species, Gobiodon histrio and G. quinquestrigatus, respectively, to determine whether gobies are selecting between intraspecific colour polymorphisms or cryptic coral species. We also examine genetic differentiation among coral populations containing both these colour morphs that are separated by metres between local sites, tens of kilometres across the continental shelf and hundreds of kilometres along the Great Barrier Reef. We use three nuclear DNA loci, two of which we present here for the first time for Acropora. No significant genetic differentiation was detected between sympatric colour morphs at these three loci. Hence, symbiotic gobies are selecting among colour morphs of A. nasuta, rather than cryptic species. Significant genetic geographical structuring was observed among populations, independent of colour, at regional (i.e. latitudinal separation by < 500 km) and cross-shelf (< 50 km) scales, alongside relative homogeneity between local populations on within reef scales (< 5 km). This contrasts with the reported absence of large-scale genetic structuring in A. valida, which is a member of the same species group as A. nasuta. Apparent differences in biogeographical structuring between species within the A. nasuta group emphasize the need for comparative sampling across both spatial (i.e. within reefs, between reefs and between regions) and taxonomic scales (i.e. within and between closely related species).

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Year:  2004        PMID: 14653784     DOI: 10.1046/j.1365-294x.2003.02019.x

Source DB:  PubMed          Journal:  Mol Ecol        ISSN: 0962-1083            Impact factor:   6.185


  9 in total

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Journal:  Coral Reefs       Date:  2018-11-08       Impact factor: 4.640

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4.  Restoration of coral populations in light of genetic diversity estimates.

Authors:  T L Shearer; I Porto; A L Zubillaga
Journal:  Coral Reefs       Date:  2009-09       Impact factor: 3.902

5.  Symbiotic associations in the phenotypically-diverse brown alga Saccharina japonica.

Authors:  Evgeniy S Balakirev; Tatiana N Krupnova; Francisco J Ayala
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6.  Genetic diversity and divergence among coastal and offshore reefs in a hard coral depend on geographic discontinuity and oceanic currents.

Authors:  Jim N Underwood
Journal:  Evol Appl       Date:  2009-02-02       Impact factor: 5.183

7.  Rarity and genetic diversity in Indo-Pacific Acropora corals.

Authors:  Zoe T Richards; Madeleine J H Oppen
Journal:  Ecol Evol       Date:  2012-07-06       Impact factor: 2.912

8.  Genetic traces of recent long-distance dispersal in a predominantly self-recruiting coral.

Authors:  Madeleine J H van Oppen; Adrian Lutz; Glenn De'ath; Lesa Peplow; Stuart Kininmonth
Journal:  PLoS One       Date:  2008-10-14       Impact factor: 3.240

9.  No variation and low synonymous substitution rates in coral mtDNA despite high nuclear variation.

Authors:  Michael E Hellberg
Journal:  BMC Evol Biol       Date:  2006-03-16       Impact factor: 3.260

  9 in total

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