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World Congress of Malacology Antwerp ... - Unitas Malacologica

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distant populations <strong>of</strong> the same morphotype again indicating that cohesion <strong>of</strong> morphotypes was<br />

mainly due to selection. The actual distribution <strong>of</strong> morphotypes and haplotypes as well as the high<br />

genetic diversity also suggested that the area provided refugia during the Pleistocene glaciations.<br />

Molecular phylogeny and morphological evolution <strong>of</strong> pholadoidean boring bivalves (Bivalvia:<br />

Myoida)<br />

Haga, Takuma 1 ; Kase, Tomoki 2<br />

1. Department <strong>of</strong> Biological Science, Graduate School <strong>of</strong> Sciences, The University <strong>of</strong> Tokyo, 7-3-1<br />

Hongo, Bunkyo-ku, Tokyo 113-0033, Japan,<br />

Email: haga@kahaku.go.jp<br />

2. Department <strong>of</strong> Geology, National Museum <strong>of</strong> Nature and Sciences, 3-23-1 Hyakunin-cho,<br />

Shinjuku-ku, Tokyo 169-0073, Japan,<br />

Email: kase@kahaku.go.jp<br />

The superfamily Pholadoidea consists <strong>of</strong> Pholadidae (piddocks) and Teredinidae (shipworms) with<br />

over 150 modern species living in the deep sea to freshwater rivers. They have unique morphologies<br />

adapted to mechanical boring into various substrata such as sand, mud, rocks and woods. A wellaccepted<br />

hypothesis on the evolutionary pathway in Pholadoidea is that the sand- and mud-borers<br />

were preceded by the wood- and rock-borers.<br />

To test this hypothesis, we reconstructed a phylogeny <strong>of</strong> Pholadoidea based on sequence data from<br />

four genes (complete 18S rRNA, partial Histone 3, 16S rRNA, and CO1) for 81 species from 26<br />

genera as an ingroup. Phylogenetic trees were constructed using MP and Bayesian method with a<br />

maximum 3,171 bp dataset, and then 60 morphological characters were parsimoniously mapped and<br />

reconstructed on the cladogram to search synapomorphies.<br />

Our result shows that Pholadidae, Xylophagainae, Jouannetiinae and Teredinidae are major clades<br />

supported by strong statistical values, and that the wood- and rock-borers with anterior-boring<br />

mechanism are ancestral while the sand- and mud-borers with ventral-boring mechanism are<br />

derivative within the Pholadoidea, which clearly contradicts the previous hypothesis. Our molecular<br />

study reveals interesting patterns <strong>of</strong> morphological evolution in the phylogeny <strong>of</strong> Pholadidae: the<br />

more generalized s<strong>of</strong>t-bottom infaunal mode <strong>of</strong> life (associated with simplified morphologies and<br />

posterior elongation <strong>of</strong> valves observed in Pholadidae) among bivalves was derived from more<br />

specialized rock- and wood-boring mode <strong>of</strong> life. The wood-boring Xylophagainae and Teredinidae,<br />

which harbor associated bacteria for xylotrophy, are phylogenetically distant to each other, suggesting<br />

that the associated bacteria was acquired independently in those groups. The Pholadoidea would have<br />

gained high species diversity by exploiting various kinds <strong>of</strong> substrata through mechanical boring<br />

rather than chemical boring.<br />

Harmonic radar evidence for wind dispersal and homing capability in the tree snail genus<br />

Achatinella (Pulmonata: Achatinellidae)<br />

Hall, Kevin T. 1 ; Hadfield, Michael G. 2<br />

1. University <strong>of</strong> Hawaii at Manoa, 2538 McCarthy Mall, EDM 152, Honolulu,<br />

Hawaii, 96822, USA, Email: kthall@hawaii.edu<br />

2. Kewalo Marine Laboratories, 41 Ahui Street, Honolulu, Hawaii, 96813, USA,<br />

Email: hadfield@hawaii.edu<br />

Conservation efforts for the endangered Achatinella tree snails, which are endemic to the island <strong>of</strong><br />

Oahu, Hawaii, will likely soon include translocations among the remaining wild and captive-bred<br />

populations. Natural dispersal rates are being determined as part <strong>of</strong> optimizing this approach and will<br />

be incorporated into models <strong>of</strong> population connectivity and gene flow. The first <strong>of</strong> three methods<br />

used for observing dispersal was harmonic radar tracking, which yielded some surprising results in<br />

addition to the intended short-term dispersal rates. Solely utilizing capture-mark-recapture (CMR)<br />

89

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