World Congress of Malacology Antwerp ... - Unitas Malacologica
World Congress of Malacology Antwerp ... - Unitas Malacologica World Congress of Malacology Antwerp ... - Unitas Malacologica
First identification of mitochondrial M genome in males of Anodonta anatina and Unio pictorum (Mollusca, Bivalvia, Unionidae) Soroka, Marianna Department of Genetics, University of Szczecin, Piastow 40b, 71-065 Szczecin, Poland, Email: marianna.soroka@univ.szczecin.pl Mitochondrial DNA (mtDNA), contrary to nuclear DNA, is inherited only maternally. This standard maternal inheritance (SMI) occurs in a majority of eukaryotic organisms. However, in marine and freshwater bivalves, another pattern of mtDNA inheritance takes place, which is named doubly uniparental inheritance (DUI). In this case, we observe two types of mitochondrial DNA: the F-type, which is inherited from the mother, and the M-type, inherited from the father. A male has both those types: the mitochondrial M-type genome, which is located in male gonads and is transmited to male progeny and the F-type of mtDNA in its somatic cells. Females usually have maternally inherited Ftype mtDNA in all their cells. The fact that DUI was found in phylogenetically remote bivalves families (Mytilidae, Veneritae, Unionidae) suggests that the phenomenon is widespread. Among unionids DUI was found in 18 species. The taxonomic restriction of the phenomenon is difficult to explain and not thoroughly studied. Many authors use somatic tissues as a source of DNA, thus obtaining only F haplotype. In these studies DNA was isolated from the gonads of male unionid specimens: Anodonta anatina and Unio pictorum. In both species the M-type mitochondrial DNA was identified through sequence analyses of the mitochondrial cytochrome oxidase subunit I (cox1) gene. Using the observed divergency method within the M-type of mtDNA, the level of inter-species genetic divergence ranged from 0 to 0.2%. The parameter was higher, up to 18%, between A. anatina and U. pictorum specimens. The sequence divergence between the M- and F-types within the cox1 gene region reached 29-32% for both species and, although very high, was still characteristic for the bivalves in which DUI had been found. In homology and phylogenetic trees M and F types form separate clades. 3D-anatomy of the rhipidoglossate heterobranchs Hyalogyrina depressa Hasegawa, 1997 and Xenoskenea pellucida Monterosato, 1874 (Gastropoda, Ectobranchia) Speimann, E.; Heß, M.; Haszprunar, G. Department Biology I, Ludwig-Maximilians-Universität München, BioZentrum Martinsried, Großhadernerstr. 2, 82152 Planegg-Martinsried, Germany, Email: erika.speimann@gmx.de; hess@zi.biologie.uni-muenchen.de; haszi@zsm.mwn.de The discovery of marine representatives of the Valvatoidea (Ectobranchia) by Ponder in 1990 established this clade as basal Heterobranchia, formerly known only from freshwater habitats. We investigated the anatomy of two marine microgastropods originally classified as Skeneidae by shell and radula characters and later transferred to the Valvatoidea as family Hyalogyrinidae: Hyalogyrina depressa from deep waters off Japan and Xenoskenea pellucida from Mediterranean shallow water. We applied computer aided 3D-reconstructions (software: AMIRA ) based on semithin section series. Both species have a tapered snout with a pair of tentacles, an anteriorly bifurcate foot, and a metapodium with a large mass of calcium cells. The mantle cavity contains an osphradium, a bipectinate, ciliated gill without bursicles or skeletal rods, and a left, pallial kidney. The rectum bypasses the monotocardian heart and shows several loops in the pallial roof. A complex, hermaphroditic genital system suggests internal fertilisation. The rhipidoglossate radula apparatus lacks cartilages, the salivary glands are long and tubular, the stomach shows a gastric shield. The nervous system is epiathroid and streptoneurous, each statocyst contains a single statolith. The eyeless Hyalogyrina depressa has a ciliated pallial tentacle at the right side. Xenoskenea pellucida has a small copulatory organ behind the right cephalic tentacle, a metapodial tentacle, and simple lens eyes. These anatomical data and the hyperstrophic larval shells all reflect basal heterobranch conditions. The metapodial calcium cells and the looped pallial rectum are interpreted as synapomorphies for the 212
Hyalogyrinidae. Their rhipidoglossate radula and the lack of cartilages suggest that the Heterobranchia as a whole emerged from the rhipidoglossate rather than from the taenioglossate level of gastropod evolution. Accordingly, a change of function in the supporting apparatus (replacement of cartilages by a muscular mass) predates the change of the radular type itself at the beginning of heterobranch evolution. Molluscan evidence of woodland disturbance in the Irish Holocene Speller, George R.; Preece, Richard C. Department of Zoology, University of Cambridge, Downing Street, Cambridge, CB2 3EJ, UK, Email: gspeller@gmail.com; rcp1001@cam.ac.uk Radiocarbon dated molluscan sequences from three extensive Irish Holocene tufa deposits have provided information relating to human impact on the environment. Work at Newlands Cross, situated in the outskirts of Dublin in the east of Ireland, builds on an earlier study, which demonstrated that this thin deposit of tufa (only about 1 m thick) covered much of the early to mid Holocene, providing the most detailed succession of land snails known from Ireland. The new work includes the analyses of five further profiles, with a much-improved sampling resolution (down to 1 cm). These have amplified aspects of faunal history and enabled further light to be shed on a Mesolithic disturbance horizon previously identified at the site. The new records suggest that the area affected by the disturbance was extremely limited (perhaps less than 50 m 2 ) and of relatively brief duration (a few hundred years). Two sites (Graffy and Cartronmacmanus) located only 3 km apart in Co Mayo in western Ireland provided less complete records for the very early Holocene but furnished excellent sequences from about 8200 yrs BP to 2000 yrs BP. The faunal successions were less dynamic than those at Newlands Cross but they too yielded evidence of woodland disturbance, this time dating from the late Bronze Age and early-middle Iron Age. The registration of at least five such events differed significantly from the characteristic faunal signatures associated with comparable impacts in southern Britain. This results from the relative scarcity in Ireland of species such as Vallonia costata, although the impacts are clearly indicated by declines in shade-demanding species, such as Discus rotundatus. Scallops visually respond to simulated particles in flow Speiser, Daniel I; Johnsen, Sönke Duke University Department of Biology, Box 90338, Durham, NC 27708, USA, Email: dis4@duke.edu; sjohnsen@duke.edu Scallops’ eyes are abundant in number and positioned along the mantle at the edges of the valves. The optical properties of these eyes have been well-studied and they are known to form relatively high-resolution images. However, the function of scallop vision remains open to debate. We tested whether scallops, which are filter feeders, use their eyes to detect suspended particles. Specimens of the Common Bay Scallop Argopecten irradians were placed in an operating flow tank and shown simulated images of moving particles. Their mantle gapes were then observed at 24 second intervals over ten minute trials. We found that 25 scallops were open in 52% ± 6% of observations when particles were shown, while 24 scallops viewing a blank screen were open in 29% ± 5% of observations. The difference between these treatments was found to be significant (P
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First identification <strong>of</strong> mitochondrial M genome in males <strong>of</strong> Anodonta anatina and Unio<br />
pictorum (Mollusca, Bivalvia, Unionidae)<br />
Soroka, Marianna<br />
Department <strong>of</strong> Genetics, University <strong>of</strong> Szczecin, Piastow 40b, 71-065 Szczecin, Poland,<br />
Email: marianna.soroka@univ.szczecin.pl<br />
Mitochondrial DNA (mtDNA), contrary to nuclear DNA, is inherited only maternally. This standard<br />
maternal inheritance (SMI) occurs in a majority <strong>of</strong> eukaryotic organisms. However, in marine and<br />
freshwater bivalves, another pattern <strong>of</strong> mtDNA inheritance takes place, which is named doubly<br />
uniparental inheritance (DUI). In this case, we observe two types <strong>of</strong> mitochondrial DNA: the F-type,<br />
which is inherited from the mother, and the M-type, inherited from the father. A male has both those<br />
types: the mitochondrial M-type genome, which is located in male gonads and is transmited to male<br />
progeny and the F-type <strong>of</strong> mtDNA in its somatic cells. Females usually have maternally inherited Ftype<br />
mtDNA in all their cells. The fact that DUI was found in phylogenetically remote bivalves<br />
families (Mytilidae, Veneritae, Unionidae) suggests that the phenomenon is widespread. Among<br />
unionids DUI was found in 18 species. The taxonomic restriction <strong>of</strong> the phenomenon is difficult to<br />
explain and not thoroughly studied. Many authors use somatic tissues as a source <strong>of</strong> DNA, thus<br />
obtaining only F haplotype. In these studies DNA was isolated from the gonads <strong>of</strong> male unionid<br />
specimens: Anodonta anatina and Unio pictorum. In both species the M-type mitochondrial DNA<br />
was identified through sequence analyses <strong>of</strong> the mitochondrial cytochrome oxidase subunit I (cox1)<br />
gene. Using the observed divergency method within the M-type <strong>of</strong> mtDNA, the level <strong>of</strong> inter-species<br />
genetic divergence ranged from 0 to 0.2%. The parameter was higher, up to 18%, between A. anatina<br />
and U. pictorum specimens. The sequence divergence between the M- and F-types within the cox1<br />
gene region reached 29-32% for both species and, although very high, was still characteristic for the<br />
bivalves in which DUI had been found. In homology and phylogenetic trees M and F types form<br />
separate clades.<br />
3D-anatomy <strong>of</strong> the rhipidoglossate heterobranchs Hyalogyrina depressa Hasegawa, 1997 and<br />
Xenoskenea pellucida Monterosato, 1874 (Gastropoda, Ectobranchia)<br />
Speimann, E.; Heß, M.; Haszprunar, G.<br />
Department Biology I, Ludwig-Maximilians-Universität München, BioZentrum Martinsried,<br />
Großhadernerstr. 2, 82152 Planegg-Martinsried, Germany,<br />
Email: erika.speimann@gmx.de; hess@zi.biologie.uni-muenchen.de; haszi@zsm.mwn.de<br />
The discovery <strong>of</strong> marine representatives <strong>of</strong> the Valvatoidea (Ectobranchia) by Ponder in 1990<br />
established this clade as basal Heterobranchia, formerly known only from freshwater habitats. We<br />
investigated the anatomy <strong>of</strong> two marine microgastropods originally classified as Skeneidae by shell<br />
and radula characters and later transferred to the Valvatoidea as family Hyalogyrinidae: Hyalogyrina<br />
depressa from deep waters <strong>of</strong>f Japan and Xenoskenea pellucida from Mediterranean shallow water.<br />
We applied computer aided 3D-reconstructions (s<strong>of</strong>tware: AMIRA ) based on semithin section<br />
series.<br />
Both species have a tapered snout with a pair <strong>of</strong> tentacles, an anteriorly bifurcate foot, and a<br />
metapodium with a large mass <strong>of</strong> calcium cells. The mantle cavity contains an osphradium, a<br />
bipectinate, ciliated gill without bursicles or skeletal rods, and a left, pallial kidney. The rectum<br />
bypasses the monotocardian heart and shows several loops in the pallial ro<strong>of</strong>. A complex,<br />
hermaphroditic genital system suggests internal fertilisation. The rhipidoglossate radula apparatus<br />
lacks cartilages, the salivary glands are long and tubular, the stomach shows a gastric shield. The<br />
nervous system is epiathroid and streptoneurous, each statocyst contains a single statolith. The eyeless<br />
Hyalogyrina depressa has a ciliated pallial tentacle at the right side. Xenoskenea pellucida has a<br />
small copulatory organ behind the right cephalic tentacle, a metapodial tentacle, and simple lens eyes.<br />
These anatomical data and the hyperstrophic larval shells all reflect basal heterobranch conditions.<br />
The metapodial calcium cells and the looped pallial rectum are interpreted as synapomorphies for the<br />
212