DIETARY INDUCTION OF OPISTHOBRANCH MORPHOLOGY: PLACIDA DENDRITICA (ALDER & HANCOCK, 1843) ON DIFFERENT GREEN ALGAL HOSTS

The relationship of phenotypic morphological and behaviouralvariation was investigated for the ascoglossan (=sacoglossan)opisthobranch Placida dendritica. Morphological attributes weredocumented for individual slugs collected from three algal hostspecies along the central Oregon coast, USA, the green algaeCodium setchellii, C. fragile, and Bryopsis corticulans. Becauseindividuals on B. corticulans generally were substantially largerthan conspecifics on Codium spp., the species appeared polymorphic.Comparably sized slugs from different host genera also differedsignificantly in morphology: individuals from Codium spp. hadmore numerous, shorter cerata on wider bodies than did conspecificsfrom B. corticulans. Principal components analysis indicatedthat despite considerable overlap of morphological characters,ceratal shape features were diagnostic of algal host. When slugscollected from C. fragile were maintained on C. fragile andB. corticulans for 4 days in the laboratory, the size and shapeof slugs fed different diets diverged, and changes were consistentwith field data. Thus, phenotype was labile and changed as aresult of modified diet. Although a variety of molluscs exhibitdietary induction of morphology, a general awareness of thephenomenon has only recently begun to emerge, despite its importantecological and taxonomic implications. (Received 5 February 1996; accepted 2 July 1996)     

FEEDING AND GROWTH OF THE AEOLID NUDIBRANCH CUTHONA NANA (ALDER AND HANCOCK, 1842)

Feeding and growth of the aeolid nudibranch Cuthona nana wasdocumented. Cuthona nana feeds specifically on the colonialhydroid Hydractinia echinata. Nudi-branchs were observed onhermit crab shells in Gos-port Harbor at the Isles of Shoals,Maine and on old bridge pilings near Gerrish Island, Maine. Grazing rates of nudibranchs (3–25 mm) were quantifiedover 24 hour periods in the laboratory. Larger nudibranchs consumedmore hydroid tissue feeding mostly on polyps, whereas smallerindividuals consumed less and fed on mat tissue. Grazing intensityin the field at Gosport Harbor was determined by estimatingthe area of grazed patches of hydroid colonies attached to hermitcrab shells. The average patch size was 5.75% of the total colonyarea. Growth rates for nudibranchs were determined in the laboratory.Growth rates were greatest prior to maturation and oviposition.Animals from Gerrish Island and Gosport Harbor decreased insize after oviposition due to senescence. Nudibranchs from GerrishIsland reached a maximum size of 12 mm, compared to 23 mm foranimals at Gosport Harbor. ^*Present address: Division of Science and Mathematics. Universityof Minnesota, Morris. Minnesota 56267, USA     

THE GROWTH OF PELTODORIS ATROMACULATA BERGH, 1880 (GASTROPODA: NUDIBRANCHIA) IN THE LABORATORY

The growth of Peltodons atromaculata Bergh, 1880, measured astotal dorsal body area, was followed in the laboratory for 15months. The growth of dorsal brown patches was compared to thetotal area of the mantle, and was shown to be approximatelyconstant over time in the different animals. This numericalapproach can be useful to quantify the body pigmentation clinepreviously described for Mediterranean specimens. P atromaculatahas an annual life-cycle in the laboratory, reaching its maximumsize before opposition. Post-spawning mortality followed a decreasein size for all specimens. Mantle margin autotoray in P atromaculataseems not to be related to defence against predation, but itis a process that takes place before death in laboratory. (Received 1 December 1994; accepted 28 April 1995)     

REVIEW OF THE GENUS DENDRODORIS EHRENBERG, 1831 (GASTROPODA: NUDIBRANCHIA) IN THE ATLANTIC OCEAN

Six valid species of the nudibranch genus Dendrodons Ehrenberg,1831 inhabit the Atlantic Ocean, including the Mediterraneanand Caribbean Seas. Dendrodons lumbata (Cuvier, 1804), Dendrodonsgrandiflora (Rapp, 1827), Dendrodons nigra (Stimpson, 1855)(immigrant from the Red Sea), Dendrodons krebsu (Mörch,1863), Dendrodoru senegalensis Bouchet, 1975 and Dendrodonswarta Marcus & Gallagher, 1976. Additional data about thebiology and geographical distribution of these species are presented.New evidence suggests that other species assigned to the genusDendrodons, Dendrodons racemosa Pruvot-Fol, 1951 and Dendrodonsminima Pruvot-Fol, 1951, must be included in the genus DoriopsillaBergh, 1880. Three new species of Dendrodoris are describedfrom the Northeastern Atlantic and West Africa;Dendrodons angolensis,Dendrodoris guineana and Dendrodons herytra. The variable external morphology makes species recognition difficult.Instead, the diagnostic characters utilised to separate speciesare the shape of the male cirrus hooks, the structure of thereproductive system and features of the egg-mass. (Received 25 April 1995; accepted 1 August 1995)     

REDESCRIPTION OF PHYLLIDIOPSIS SINAIENSIS (YONOW, 1988) (NUDIBRANCHIA: DORIDOIDEA: PHYLLIDIIDAE), WITH A REVIEW OF THE RED SEA PHYLLIDIIDAE

Phyllidiopsis sinaiensis (Yonow, 1988), of which only one single preservedspecimen had been known, was rediscovered in the northern RedSea. The dorsal colour-pattern of living individuals is presented forthe first time, and the anatomy of P. sinaiensis is describedin detail. Major features of the holotype previously used tocharacterise the species are shown to be artifacts. Principaldistinguishing characters of P. sinaiensis include the centraltubercle ridge, large and multicompound, broad based, pink tubercles,bicoloured black and pink rhinophores, the very elongate muscularoesophageal segment, the distinct stomach and the extremelylong, convoluted prostate that is bound together by connectivetissue. In some specimens, the bases of the tubercles may fuseleading to a predominantely pink dorsum with only a few blacklines. Phyllidiopsis sinaiensis appears to be among the mostcommon nudibranchs in the Gulf of Aqaba. The fact that it has notbeen reported since its original collection in 1980 can be explainedby being confused with the externally similar, well-known speciesPhyllidiella pustulosa (Cuvier, 1804). A review of the phyllidiidfauna of the Red Sea reveals eleven valid species that can allbe identified with the key presented herein. With four out of elevenspecies, phyllidiid endemism (36%) is high in the Red Sea. This isin contrast to recent palaeobiological hypotheses of a post-glacial originof the Red Sea coral reef fauna.     

ANATOMY OF PSEUDOTRITONIA THIELE, 1912 AND NOTAEOLIDIA ELIOT, 1905 (GASTROPODA: OPISTHOBRANCHIA: NUDIBRANCHIA) FROM SIGNY ISLAND, ANTARCTICA

Several species of nudibranch molluscs are abundant amongstthe rich benthic hard substratum communities found close tothe British Antarctic Survey base at Signy Island, in the Atlanticsector of the Antarctic. Over the austral summer 1992/1993,two of the authors (LWB and DKAB) were able to collect someof the lesser known species of Nudibranchia at depths between3 and 40 metres, using SCUBA. New information on morphologyand anatomy of two of these species, Pseudotritonia gracilidensOdhner, 1944 (Charcotiidae, Arminoidea) and Notaeolidia gigasEliot, 1905(Notaeolidiidae, Aeolidoidea) are presented in thispaper. The validity of the species Notaeolidia gigas is strengthened. (Received 9 February 1994; accepted 18 September 1994)     

REDESCRIPTION OF EMBLETONIA GRACILE RISBEC, 1928 (NUDIBRANCHIA: EMBLETONIIDAE): RELOCATION TO SUBORDER DENDRONOTACEA WITH TAXONOMIC AND PHYLOGENETIC IMPLICATIONS

The nudibranch mollusc Embletonia gracile Risbec, 1928 is redescribedon the basis of ten specimens from the southern Pacific Ocean(New Zealand, Fiji, Australia, Papua New Guinea). We concludethat Embletoniella paucipapillata (Baba & Hamatani, 1963)is a junior synonym. Even the most detailed previous studieswere compromised by the availability only of juvenile animals< 8 mm long; adults are now known to attain 23 mm crawlinglength. Our material permitted a reassessment both of ontogeneticand intraspecific variation within this enigmatic nudibranch.Reasons that substantiate the referral of the Embletoniidaeto the suborder Dendronotacea are presented. (Received 20 February 1991; accepted 10 May 1991)     

MORPHOLOGY OF THE MATURE SPERMATOZOON OF PHYSA ACUTA (DRAPARNAUD, 1801) (GASTROPODA: PHYSIDAE)

The morphology of the spermatozoon of Physa acuta (Draparnaud,1801) was examined using TEM. It was found to be of the modified-type,sharing characteristic features of other basommatophoran species.However, differences were noted in some cases, for example,in P. acuta the nucleus was torpedo-shaped with two helicalkeels, the midpiece possessed a maximum of three glycogen helices,the end piece was long and tapered and the total length of thespermatozoon was 365 µm. No identical spermatozoa havebeen found in other basommatophoran gastropods studied so far.If spermatozoon morphology is unique for individual specieswithin the genus Physa, it may provide a useful taxonomic toolin helping to clarify the uncertainty that surrounds the systematicsof this genus. (Received 26 February 1990; accepted 28 June 1990)     

FOUR NEW SPECIES OF TAMBJA BURN, 1962 (NUDIBRANCHIA: POLYCERIDAE) FROM THE INDO-PACIFIC

The genus Tambja previously included 24 described species. Fournew species, T. tentaculata n. sp., T. gabrielae n. sp., T.zulu n. sp. and Tambja victoriae n. sp., from the Indo-Pacificare described. Tambja tentaculata n. sp., from Guam, is theonly known species in the genus with well developed, dorsolaterallygrooved, oral tentacles. Its inner lateral teeth have a bifidinner cusp with two long, sharp denticles. The oral tentaclesof T. tentaculata are more typical of Roboastra species, whilethe shape of the inner lateral teeth is more typical of Tambja.Nevertheless, the arrangement of the two cusps of the innerlateral teeth and the presence of a rachidian tooth withoutdenticles and with a central notch at the anterior edge, typicalof the species of the genus Tambja, suggest the placement withinthis genus. Tambja gabrielae n. sp., from Indonesia and PapuaNew Guinea, has dark green to dark brown ground colour withbright yellow patches scattered on the body. Tambja zulu n.sp. from Durban, South Africa, is characterized by a black groundcolour with slender yellow longitudinal lines. Tambja victoriaen. sp. is a new species from Papua New Guinea and Australiathat has frequently been misidentified as Roboastra arika, characterizedby its blue body colour and yellow lines. The four species aredistinguishable based on differences in body coloration, ofcharacters of the radula and of the reproductive system. Anoverview on distinguishing features of all known Indo-PacificTambja species is presented. (Received 21 June 2004; accepted 20 January 2005)     

THYSANODONTINAE: A NEW SUBFAMILY OF THE TROCHIDAE (GASTROPODA)

New genera Thysanodonta, Carinastele and Herbertina are referredto a new subfamily of the Troch-idae, Thysanodontinae, on thebasis of extremely distinctive jaw and radula. At up to 1400times longer than broad, the teeth are the most slender of anyknown gastropod, and they are unique among archae-ogastropodsin having harpoon-like tips with back-wardly inclined barbs.While food and feeding mode are unknown, it is suggested thatthey feed suctorially, perhaps on cnidarians. New species describedare Thysanodonta aucklandica, T. wairua, Carinastele kristelleae,C. jugosa, and C. coronata from New Zealand, T. boucheti fromNew Caledonia, and Herbertina eos and H. cognata from SouthAfrica. The Tasmanian Basilissa nicetarium Hedley & Mayis tentatively referred to Carinastele (Received 23 September 1987;     

海洋纤毛虫--水滴伪康纤虫的口器发生及形态学重描述

利用蛋白银法对采自山东胶州育虾池的一种海洋盾纤类纤毛虫,水滴伪康纤虫(Pseudocohnilembus persalinus Evans&Thompson,1964)的口器发生过程进行了详细的观察和研究,并对其形态学做了补足性描述。文章通过对该青岛种群发生过程的研究,认为前人所报道的种群(Evans&Thompson,1964;Pomp&Wilbert,1988)缺乏对某个发生关键时期的观察而存在着错误,即:后仔虫的小膜2明确来自老的口侧膜,而不是前人报道的盾片。此外,文章还发现该种的发生与本属另一哈氏伪康纤虫的发生过程几乎完全相同。主要细胞发生过程为:盾片最先增殖,形成初级原基区,然后分裂成前后两部分,前部分最终消失,而后部分最终形成后仔虫的小膜3。继盾片增殖之后口侧膜的锯齿状结构沿细胞纵轴方向分裂成两列,右侧的一列增殖形成次级原基区,之后分裂成前后两部分,前部分迁移形成后仔虫的口侧膜和盾片,后部分形成后仔虫的小膜1和小膜2;老口侧膜的残余部分形成前仔虫的口侧膜及盾片。老的小膜1、小膜2和小膜3则完全为前仔虫所继承。