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World Congress of Malacology Antwerp ... - Unitas Malacologica

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keys for micromollusc samples: The distinction <strong>of</strong> immature stages <strong>of</strong> larger species and adults <strong>of</strong><br />

smaller species is critical in most groups except for those showing the sign <strong>of</strong> maturity in the shell<br />

(determinate growth).<br />

Anatomy <strong>of</strong> Eulepetopsis vitrea McLean, 1990 (Patellogastropoda: Neolepetopsidae)<br />

Sasaki, Takenori 1 ; Warén, Anders 2<br />

1. The University Museum, The University <strong>of</strong> Tokyo, 7-3-1 Hongo, Bunkyo-ku, Tokyo 113-0033,<br />

Japan,<br />

Email: sasaki@um.u-tokyo.ac.jp<br />

2. Swedish Museum <strong>of</strong> Natural History, Box 50007, SE-10405 Stockholm, Sweden<br />

Neolepetopsidae is one <strong>of</strong> families newly discovered from hydrothermal vents in the late 20th<br />

century. It was originally classified as an independent suborder (Lepetopsina) in Patellogastropoda,<br />

but such treatment was questioned by subsequent authors. To obtain more detailed evidence for<br />

phylogenetic estimation, we investigated the anatomy <strong>of</strong> Eulepetopsis vitrea, using gross dissection,<br />

serial sectioning and scanning electron microscopy. As a result, the animal <strong>of</strong> E. vitrea was revealed<br />

to possess the following features: short-type pallial margin tentacles, mouth surrounded by oral<br />

lappet, pedal wall lacking pallial ridges, ctenidium and osphradia entirely missing, unique<br />

configuration <strong>of</strong> alimentary tract, reduced salivary glands, small angle <strong>of</strong> oesophageal torsion, paired<br />

openings into digestive glands, acmaeoidean-type buccal musculature, dorsal protractor muscle <strong>of</strong><br />

odontophore thin and widely covering buccal mass, two pairs <strong>of</strong> odontohporal cartilages, ventrally<br />

positioned thin approximator muscle, rectum bypassing ventricle, statocysts attached to outer lateral<br />

side <strong>of</strong> pleural ganglia, deeply ramified testis but massive ovary. The combination <strong>of</strong> above<br />

characters suggests the possible relationships with deep-sea Acmaeoidea (e.g. Bathyacmaea,<br />

Pectinodonta or some lepetids). In contrast, the closeness to Patelloidea (Patellidae and Nacellidae) is<br />

clearly rejected by the fact that there is no uniquely shared character among three families. Further<br />

anatomical investigations are necessary for unstudied subtidal and deep-sea groups (e.g. Acmaea,<br />

Serradonta, many lepetids) to understand the phylogeny <strong>of</strong> whole patellogastropods.<br />

Comparative analysis <strong>of</strong> land snail radiations on Crete<br />

Sauer, Jan; Hausdorf, Bernhard<br />

Zoological Museum, University <strong>of</strong> Hamburg, Martin-Luther-King-Platz 3, D-20146 Hamburg,<br />

Germany, Email: ja_sa@web.de; hausdorf@zoologie.uni-hamburg.de<br />

To investigate the causes for the land snail radiations on Crete we studied the systematics and<br />

phylogeny <strong>of</strong> the radiation <strong>of</strong> the genus Xerocrassa on Crete using morphological characters,<br />

mitochondrial (cox1, 16S rDNA) and nuclear (ITS2) DNA sequences and AFLP markers. Twelve<br />

Xerocrassa species occur on Crete, six <strong>of</strong> which have not been described so far. Distribution maps <strong>of</strong><br />

these species were based on almost 3000 records. With these data and corresponding data on other<br />

Cretan land snail radiations, especially <strong>of</strong> the genera Mastus and Albinaria, we tested the hypothesis<br />

that these radiations were the result <strong>of</strong> a fragmentation <strong>of</strong> Crete into several paleoislands during the<br />

late Miocene and Pliocene. Contrary to the predictions <strong>of</strong> this hypothesis, Monte Carlo simulations<br />

showed that the distribution areas <strong>of</strong> the Cretan endemics are not significantly clustered and the<br />

phylogenies <strong>of</strong> the radiations do not reflect a common pattern. These results indicate that the land<br />

snail radiations on Crete were not caused by a common sequence <strong>of</strong> vicariance events. Probably,<br />

stochastic events like chance colonization <strong>of</strong> isolated habitats were more important. Although most<br />

sister clades <strong>of</strong> Cretan Xerocrassa species are allopatric and show strong range size asymmetry as<br />

predicted by the peripatric speciation model, a test for peripatric speciation based on a Monte Carlo<br />

simulation <strong>of</strong> range size asymmetry was non-significant. This indicates that different speciation<br />

modes might have been involved in the radiation <strong>of</strong> Cretan Xerocrassa species. Hardly any habitat<br />

differences between Cretan Xerocrassa species can be identified. Thus, the radiation is apparently<br />

195

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