World Congress of Malacology Antwerp ... - Unitas Malacologica
World Congress of Malacology Antwerp ... - Unitas Malacologica World Congress of Malacology Antwerp ... - Unitas Malacologica
Interstitial Mollusca of the amphioxus sand of the Galician Coasts (NW Iberian Peninsula) Urgorri, Victoriano 1,2 ; García-Álvarez, Oscar 1 ; Corral, Eva 1 ; Díaz-Agras, Guillermo 2 ; Candás, María 2 ; Señarís, Marcos P. 1 ; Botana, Alba G. 1 1. Departamento de Zooloxía e Antropoloxía Física, Facultade de Bioloxía, Universidade de Santiago de Compostela, Spain, Email: bavituco@usc.es 2. Estación de Bioloxía Mariña da Graña, Rúa da Ribeira 1, 15590-Ferrol, Universidade de Santiago de Compostela, Spain The results of the researches carried out about the malacological components of the interstitial fauna of three infralittoral banks of amphioxus sands of the Galician coasts are presented herein. Solenogastres: Biserramenia psammobionta Salvini-Plawen, 1967, Meioherpia sp.; Prosobranchia: Caecum glabrum (Montagu, 1803); Opisthobranchia: Philinoglossa helgolandica Hertling, 1932, Hedylopsis spiculifera (Kowalevsky, 1901), Asperpina loricata (Swedmark, 1968), Unela glandulifera (Kowalevsky, 1901), Pseudovermis artabrensis Urgorri, Cobo & Besteiro, 1991, Embletonia pulchra Alder & Hancock, 1851 and two tiny species of. Doridacea found in these sands. All the studied material comes from three infralittoral banks of amphioxus sands, of which two are placed on the Ría of Ferrol and one on the Ría of Arousa (Galicia, NW Iberian Peninsula), located between 11 and 25 m depth. The specimens were sorted out by dipping a portion of sediment into a solution of Cl2Mg at 5% (50% seawater and fresh water) for 5 minutes. The sediment was then put into water, shaked and quickly decanted onto a tower of three sieves with a netting of 500, 250 y 100 µm respectively. The external anatomy, the radular system at SEM and the geographic arrangement are described in each species. Besides, the taxonomical position of the specimens of the two Doridacea species according to their particular anatomical features is needed. Finally, it is discused if these are either young specimens of known species or new species, as well as if they are young specimens or if, on the contrary, they are adults of interstitial species, taking into account that no Doridacea have been ever described so far in this environment. Biogeographical analysis of a molluscan hotspot in the Alboran Sea Urra, Javier; Gofas, Serge; Marina, Pablo; Rueda, José L. Laboratorio de Invertebrados Marinos, Departamento de Biología Animal, Universidad de Málaga, Campus de Teatinos s/n, 29071, Málaga, Spain, Email: urra_sp@yahoo.es, sgofas@uma.es, pablo_marina@eresmas.com, jlruedaruiz@yahoo.es The Alboran Sea represents a crossroad between Atlantic and Mediterranean waters, where upwellings and mixing of waters take place and define different sectors with genuine characteristics. The hydrology is strongly influenced by the geomorphology of the Strait of Gibraltar, resulting in a conspicuous gyre of superficial waters of Atlantic origin. All these factors favour the coexistence of species from both basins. A survey covering different types of bottoms has been carried out on a short stretch of coastline (10 km) between Punta de Calaburras (36º30’4'N - 04º38’W) and Cabo Pino (36º28’N -04º44’W) (Malaga, southern Spain). Objectives were to assess the composition of the molluscan fauna in this area, to evaluate the need for its protection and to study the biogeographical affinities of the species. A total of 329 species of molluscs were found. Their shared presence in the following six sectors has been considered: (1) northern Europe, (2) western Europe (between the Channel and Portugal), (3) Ibero-Moroccan Gulf, (4) Canary Islands, (5) tropical West Africa (south of Cap Blanc, Mauritania) and (6) Mediterranean Sea. Most of the species have a wide Atlantic-Mediterranean distribution (219 spp.; 67.8 %), whereas 65 spp. (~ 20 %) are Mediterranean and only 9 spp. (2.8 %) are shared with the Atlantic coasts of Europe and not with the Mediterranean. The tropical West African fauna is 226
epresented by 23 spp. (7.1 %) and there are 8 endemic species (2.4 %) from southern Spain or the Ibero-Moroccan area. The diversity of the molluscan fauna, possibly the highest in European waters for a single locality, is favoured by variety of habitats but also by drawing from different biogeographic origins. The presence of upwellings may also explain the rather large share of West African species, which is surprising considering the rather cool temperatures of surface waters. Valve ultrastructure of suborder Ichnochitonina (Polyplacophora) from the South West Atlantic Urteaga, Diego; Pastorino, Guido Museo Argentino de Ciencias Naturales, Av. Angel Gallardo 470, 3º Piso, Lab. 57. C1405DJR. Buenos Aires, Argentina, Email: diegourteaga@macn.gov.ar; gpastorino@macn.gov.ar The ultrastructure of the intermediate valves of Plaxiphora aurata (Spalowsky, 1795) (Mopaliidae), Chaetopleura isabellei (d'Orbigny, 1841) (Ischnochitonidae, Chaetopleurinae), Callochiton puniceus (Gould, 1846) (Ischnochitonidae, Callochitoninae) and Tonicia lebruni (Rochebrune, 1887) (Ischnochitonidae, Lepidochitoninae), collected along the Argentine coast, was studied based upon different sections, i.e., transversal, sagittal, exsagittal, diagonal and parallel to the surface. Four main layers were found: tegmentum, articulamentum, p. hypostracum and myostracum, according to terminology described by Hass (1972). The tegmentum is the outermost layer. It covers the dorsal surface of the valves and eventually folds at boundaries. This layer is made up of micro crystals without evident order, although in the upper portion it seems to form spherulitic sectors. The p. hypostracum shows a greater development in the jugal area, occupying most of its thickness. It has a crossed lamellar arrangement with its long horizontal axis normally to the sagittal axis of the chiton, although this orientation becomes somewhat disorganised when thin prismatic layers pass through the p. hypostracum. Muscles are inserted in the myostracum, which is made up of crystals arranged prismatically with their longer axis almost normal to the ventral surface of the valve. The articulamentum, which is imbedded into the soft tissues of the chiton, is made of micro crystals that diverge from the centre towards the dorsal and ventral sides, becoming almost parallel to each other. Differences among the species studied are discussed. In addition, these features are compared with those observed by Bøggild (1930) and Haas (1972) for other chiton species. Genetic basis of adaptive evolution of left-right reversal under developmental constraint Utsuno, Hiroki; Asami, Takahiro Department of Biology, Shinshu University, Matsumoto 390-8621, Japan, Email:t04h151@shinshu-u.ac.jp; asami99@shinshu-u.ac.jp The animal rule of directional asymmetry in developmental polarity indicates the presence of selection against left-right reversal. If developmental constraint stabilizes the left-right polarity in snails, how sinistral snails have repeatedly evolved? Our study answers this question. Sinistral variants of Lymnaea stagnalis hatch poorly, and hatchlings do not grow in the exact mirror-image of dextrals, even if they share nuclear genome from the same parents. This example of developmental constraint against sinistrality may result from distortion due to pleiotropy (side-effects) of the leftright determinant or to left-right reversed morphogenesis. To determine the cause, we crossed a racemic mutant with the wild dextral type in a simultaneous hermaphrodite Bradybaena similaris. The racemic mutant produces both dextral (RD) and sinistral (RS) offspring that share cytoplasmic factors from the same mother. The wild type produces only dextrals (WD). We found that only RS exhibit significantly reduced hatching success and flattened shell shape compared to RD and WD, despite sharing nuclear genes from the same parents. Because RD does not exhibit those effects of 227
- Page 255 and 256: The limited number of taxa sampled
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- Page 335 and 336: AUTHOR INDEX Abbes, I. 1 Abbott, C.
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epresented by 23 spp. (7.1 %) and there are 8 endemic species (2.4 %) from southern Spain or the<br />
Ibero-Moroccan area.<br />
The diversity <strong>of</strong> the molluscan fauna, possibly the highest in European waters for a single locality, is<br />
favoured by variety <strong>of</strong> habitats but also by drawing from different biogeographic origins. The<br />
presence <strong>of</strong> upwellings may also explain the rather large share <strong>of</strong> West African species, which is<br />
surprising considering the rather cool temperatures <strong>of</strong> surface waters.<br />
Valve ultrastructure <strong>of</strong> suborder Ichnochitonina (Polyplacophora) from the South West<br />
Atlantic<br />
Urteaga, Diego; Pastorino, Guido<br />
Museo Argentino de Ciencias Naturales, Av. Angel Gallardo 470, 3º Piso, Lab. 57. C1405DJR.<br />
Buenos Aires, Argentina,<br />
Email: diegourteaga@macn.gov.ar; gpastorino@macn.gov.ar<br />
The ultrastructure <strong>of</strong> the intermediate valves <strong>of</strong> Plaxiphora aurata (Spalowsky, 1795) (Mopaliidae),<br />
Chaetopleura isabellei (d'Orbigny, 1841) (Ischnochitonidae, Chaetopleurinae), Callochiton puniceus<br />
(Gould, 1846) (Ischnochitonidae, Callochitoninae) and Tonicia lebruni (Rochebrune, 1887)<br />
(Ischnochitonidae, Lepidochitoninae), collected along the Argentine coast, was studied based upon<br />
different sections, i.e., transversal, sagittal, exsagittal, diagonal and parallel to the surface. Four main<br />
layers were found: tegmentum, articulamentum, p. hypostracum and myostracum, according to<br />
terminology described by Hass (1972).<br />
The tegmentum is the outermost layer. It covers the dorsal surface <strong>of</strong> the valves and eventually folds<br />
at boundaries. This layer is made up <strong>of</strong> micro crystals without evident order, although in the upper<br />
portion it seems to form spherulitic sectors. The p. hypostracum shows a greater development in the<br />
jugal area, occupying most <strong>of</strong> its thickness. It has a crossed lamellar arrangement with its long<br />
horizontal axis normally to the sagittal axis <strong>of</strong> the chiton, although this orientation becomes<br />
somewhat disorganised when thin prismatic layers pass through the p. hypostracum. Muscles are<br />
inserted in the myostracum, which is made up <strong>of</strong> crystals arranged prismatically with their longer axis<br />
almost normal to the ventral surface <strong>of</strong> the valve. The articulamentum, which is imbedded into the<br />
s<strong>of</strong>t tissues <strong>of</strong> the chiton, is made <strong>of</strong> micro crystals that diverge from the centre towards the dorsal<br />
and ventral sides, becoming almost parallel to each other. Differences among the species studied are<br />
discussed. In addition, these features are compared with those observed by Bøggild (1930) and Haas<br />
(1972) for other chiton species.<br />
Genetic basis <strong>of</strong> adaptive evolution <strong>of</strong> left-right reversal under developmental constraint<br />
Utsuno, Hiroki; Asami, Takahiro<br />
Department <strong>of</strong> Biology, Shinshu University, Matsumoto 390-8621, Japan,<br />
Email:t04h151@shinshu-u.ac.jp; asami99@shinshu-u.ac.jp<br />
The animal rule <strong>of</strong> directional asymmetry in developmental polarity indicates the presence <strong>of</strong><br />
selection against left-right reversal. If developmental constraint stabilizes the left-right polarity in<br />
snails, how sinistral snails have repeatedly evolved? Our study answers this question. Sinistral<br />
variants <strong>of</strong> Lymnaea stagnalis hatch poorly, and hatchlings do not grow in the exact mirror-image <strong>of</strong><br />
dextrals, even if they share nuclear genome from the same parents. This example <strong>of</strong> developmental<br />
constraint against sinistrality may result from distortion due to pleiotropy (side-effects) <strong>of</strong> the leftright<br />
determinant or to left-right reversed morphogenesis. To determine the cause, we crossed a<br />
racemic mutant with the wild dextral type in a simultaneous hermaphrodite Bradybaena similaris.<br />
The racemic mutant produces both dextral (RD) and sinistral (RS) <strong>of</strong>fspring that share cytoplasmic<br />
factors from the same mother. The wild type produces only dextrals (WD). We found that only RS<br />
exhibit significantly reduced hatching success and flattened shell shape compared to RD and WD,<br />
despite sharing nuclear genes from the same parents. Because RD does not exhibit those effects <strong>of</strong><br />
227