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First records of the genus Berghia Trinchese, 1877 (Opisthobranchia: Aeolidiidae) from Argentina, with description of a new species PDF

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Preview First records of the genus Berghia Trinchese, 1877 (Opisthobranchia: Aeolidiidae) from Argentina, with description of a new species

Avicennia, 1999, 10/11: 143-150 First records ofthe genusBerghia THnchese, 1877 (Opisthobranchia: Aeolidiidae) from Argentina, with description ofa new species Primerregistro delgénero Berghia Trínchese, 1877(Opisthobranchia: Aeolidiidae)para Argentina, descripción de una nueva especie Claudia Muniain* and Jesús Ortea** *MuseoArgentinode CienciasNaturalesBernardinoRivadavia. LaboratoriodeMalacolo- gíayEcosistemas Costeros. Angel Gallardo470. (1405). BuenosAires, Argentina. **DepartamentodeBiologíade OrganismosySistemas. Universidadde Oviedo. España. Abstract ThereisconsiderableconfusiónamongthespeciesofaeolidnudibranchfromtheWestern AtlanticassignedtotheEuropeanBerghiacoemlescens(Laurillard, 1830),Berghiaverruci- cornis (DaCosta, 1867) andSpurillaneapolitana (Delle Chiaje, 1823. The genus Berghia Trínchese, 1877isrecordedatthefirsttimefromArgentina.Ourmaterialiscomparedanddis- cussedwithspeciesofBerghiafromtheAtlanticandMediterraneancoasts.Weconsiderthat B. coemlescensdoes notoccurintheWestAtlantic, while the western ocurrence ofB. ve- rrucicornis requires further investigation. Berghia rissodominguezi is described as a new specieswithaWesternAtlanticdistributionfromCaribbeantoNorthPatagonianwaters.The species Spurilla columbina García-Gómez and Thompson, 1990 is included in the genus BerghiaanditsdistributionisextendedtotheCanaryIsland. Resumen ExisteunagranconfusiónentrelasespeciesdenudibranquiosaeolidáceosdelAtlán- ticoOesteasignadasalasespecieseuropeasB. coemlescens(Laurillard, 1830),B. verruci- comis(Costa, 1867)andS. neapolitana(DelleChiaje, 1823).ElgéneroBerghiaTrínchese. 1877escitadoporprimeravezparaArgentina.Nuestromaterialescomparadoydiscutido conespeciesdeBerghiadelacostaAtlánticayMediterránea. LadistribucióndeB. coem- lescensparaelAtlánticoOesteesconsideradaincorrecta,mientrasqueladeB. verrucicor- niscomoespecieanfiatlántica,requieredeinvestigacionesfuturas. Seincluyealaespecie SpurillacolumbinaGarcía-GómezandThompson, 1990dentrodelgéneroBerghia,exten- diendosudistribuciónhastalasIslasCanarias. Palabrasclave: Aeolidiidae,Berghia,newspecies,SouthAtlantic,Argentina. Keywords: Aeolidiidae,Berghia,nuevaespecie,AtlánticoSur,Argentina. INTRODUCTION The validity ofthe nudibranch gastropod genera Spurilla Bergh, 1864 and Berghia Trínchese, 1877 hasbeen questionedby several authors: Rudman (1982) was the first to considersynonymisingthem. Hepointsoutthattheonly morphological difference between these generaistheposteriorornamentation on therhinophores, which are lamellated in Spu- rilla (Eolisneapolitana Delle Chiaje, 1823, type species by monotypy) and papillated in Berghia (Eolidia coemlescens (Laurillard, 1830), type species by monotypy). He didnot considered this sufficient difference to sepárate twogeneraand declared Berghia to be a júnior synonym ofSpurilla, concluding that the Aeolidiidae genera needed a complete revisión. 143 MuniainyOrtea Gosliner (1980, 1985) attempted to clarify the characteristics ofthis family, and he concluded that these genera should remain distinct until more consistent differences are discovered. Several authors (CerveraandGarcia-Gomez, 1986; Cerveraetal., 1988; Garcia-Gomez and Thompson, 1990), however, have not adopted Gosliner's sugges- tion,buthavefollowedRudman's-synonymywithoutcontributinganyadditionalevidence. On the other hand, in the Western Atlantic numerous records ofboth genera have beencitedfromtheBraziliancoast(MacFarland, 1909; Marcus, 1955, 1957, 1976; Ríos, 1994), the Caribbean Sea (Edmunds, 1964; Marcus & Marcus, 1970; Thompson, 1980; Edmunds and Just, 1983) and Florida coasts (Marcus, 1972). All ofthese re- cords havebeen assignedtothe European speciesBerghia coerulescens,B. verrucicornis (Da Costa, 1867) and Spurilla neapolitana, which have therefore been considered as amphiatlantic species. However, there are doubts as to the wisdom ofthis conclusión, because some reports ofthese species are not consistent with the description given by Tardy (1962), who demonstrated that in Europe there are in fact two species ofBerg- hia. In the present paper we compared and discussed the species ofthe genus Berghia recordedatthefirsttime inArgentinawiththe speciesconsideredamphiatlantic until now. MATERIALANDMETHODS ThespecimensstudiedcomefromMuséumNationald'HistoireNaturelle,París(MNHN),ma- terial conserved in the Laboratorio de Zoología, Universidad de Oviedo (LZUO) and specimens collectedfromPatagonia(Argentina). Risso-DomínguezdepositedinMNHN(3March 1963),onespecimenlabelledas holotype:Berg- hiapuelchana from Mar del Plata Port (Buenos Aires). This nominal species are considered no- men nudum,becausetheoriginal description hasnotbeenfound. Five specimensofBerghia were collectedfromGulfofSanJosé(PenínsulaValdés),between 1992/1995. Wealsoexaminedadditional materialofBerghiafromdifferentlocalitiesdepositedinLZUO. mm B. verrucicornis: El Puntal (Asturias) 27 Jan. 1978, 1 specimen 7 preserved length, Coll. J. mm Ortea.Melenara(LasPalmas,CanaryIslands) 10Mar. 1981, 1 specimen8 preservedlength,Coll. mm R. Castillo. Príncipe Island (GulfofGuinea) 16 Feb. 1990, 1 specimen 7 preserved length, mm Coll. X. Fernández.B. coerulescens: PuntaMagenesi (Sicily)5Jun. 1990, 1 specimen 12 pre- servedlength,Coll.G. Rodríguez. Spurillacolumbina: BarrancoHondo,Tenerife (CanaryIsland) 7 Aug. 1996, 1 specimen 34mmpreservedlength, Coll. L. Moro. Family AEOLIDIIDAE d'Orbigny 1834 Genus Berghia Trínchese, 1877 Berghiarissodominguezi new species (Fig. 1-2,Píate 1) Berghiacoerulescens(Laurillard, 1830): Marcus, 1957: 477, figs. 237-246; Edmunds, 1964: 29-30;Marcus, 1976: 9. Berghiaverrucicornis(Costa, 1864): Marcus, 1972: 304-305; Marcus, 1977: 16;Thompson, 1980: 97; Ríos, 1994: 220,fig. 1090,pl. 76. ?Berghiasp. (A,C)Edmunds, 1968: 213-217, fig. 8-9. Material examined: Mardel Plata (38°2'11"S, 57°31'37"W, Buenos Aires) intertidal zone, 18Jan. 1961, 1 specimen50mm long inlife (MNHN), Coll. C. RissoDomínguez. Patagonia, in- tertidal zone, specimens studied live from Gulf of San José (42°25'S, 64°19'W, Chubut), the length including thetail is: 23 Jan. 1992, 1 specimen 31 mmin length, Coll. C. Muniain; 28Nov. 144 NuevaespeciedelgéneroBerghia mm mm 1993, 2 specimens45 and50 inlength(dissected),Coll.C. Muniain; 13 Dec. 1995, 2spe- cimen48 mmlengthand52 mm,Coll. J. PérezBarbería. Typematerial: Holotype (depositedinMNHN, 13/12/95, 52 mm long, notdissected). mm Description: External features: Living animal thin and elongate, 52 in length (Holotype, MNHN, Pl 1A). General body colour translucent white. There are oblique bright orange lines on the borders ofthe insertion of the cerata and in front of the rhi- nophores. Overthe head andbetween the rhinophores is an orange triangle. Translucent ceras with central reddish-brown diverticulum, ending in a short white cnidosac. An orange band with a thin subapical red ring around it are present. The digestíve gland forms a brown-red dorsal digestive mid-dorsal line, visible through the mantle surface fromthe thirdgroupofceratabacktothe lastcerata. Rhinophores are long, tuberculateon the lateral andposteriorsides, withcream-whitecoloration andyellow on apical portion. The translucent oral tentacles have a wide áreaofthe same yellow colourcovering two- thirds ofthem. The tentacles are long and slender, and approximately twice as long as the rhinophores. Ceratacylindrical andelongate with arounded apex, uniform in diame- ter throughout most of their length (Fig. 1A). There are 6-8 clusters ofcerata on each side, containing between 3 to 24cerataperarch. The anteriormostclustershows the gre- atest numberofcerata21-24 (holotype) andthe mostcurved shape, decreasing in number and length towards the tail. The posterior 1-2 clusters consistofrows 1-3 cerata. The in- conspicuous renopericardical prominence is situatedbetween the first and second cerata arch, which are further apart than the others. Foot grooved anteriorly, with elongated foot cornersandtaperinggraduallytothetail. Internal anatomy: The radulaofaspecimen 50 mmlength (MNHN) contains 27 teeth with 47-50 deeply pectinate denticles on each side ofthe triangularcentral cusp. The in- nermost denticles are short so that theprofile ofthe toothis notched; the outermostden- mm ticles are uniform in shape (Fig. 2 A).Thejaws are elongate (1.2 long) with a fra- güe, smooth masticatory border. The salivary glands are shorterthan the buccal mass. The genital apertures are situated centrally in the first ceratal arch, while the anus is located within the second arch on the left side. The nephroproct is pre-anal, ventral and anteriortothe secondceratal arch. Internally, theovotestisconsistof many globularlobe which decrease in size towards thetail. Aconspicuous ampulla(8 mmlengthand 1.2 mm width), lies on topoftherestoftheorgans, andisconnectedtoanovoid seminal recepta- ele. Theprostateiselongated, expandinginto adeferentduct,buttheconjunction between the twois notwell delimited. The ductis ends in aroundedpenial papillae (Fig. IB, C). Distribution and Biology: Berghia rissodominguezi is only known from the West Atlantic, the north and south limits ofits distribution are Florida (Marcus, 1972) and the GulfofSan José, respectively. This species inhabits warm waters, and can be found understones in intertidal pools. Itisnotascommon in PatagoniaasSpurilla whichcan be collected large numberin the same time (summer). When being handled, Berghia risso- dominguezi is more prone to ceras autotomy than is S. neapolitana. Etymology: The species is named in honour ofCarlos Risso Domínguez, who co- llected the first specimen known as Berghia from Argentina. 145 = Muniain Ortea > Figure 1. Berghiarissi\hwtingucz¡newspeeies.A.Dorsalviewofalivinganimal,(scalebar=7 mmVR-C,Dorsalviewofüiegenitalsvstem. B:a,ampulla:al.albumengland: f. témalegland: ov.ovotestis.C:a.ampulla:f.femalegland:pp.pernalpapilla:pr.prostate;sr.seminalrecepta- ele:va.vagina. Figura l. Berghiarissodomingueziespecienueva.A, Mstadorsaldeunanimalvivo. (escala 7mmJLB-C. Mstadorsaldelsistemagenital* B:a,ampolla:aiglánduladelalbumen:/,glándula femenina:ov.oxxHestis. C:a.ampolla:/,glándulafemenina:pp.papilapeneal:pr.próstata:sr. receptáculoseminal:va. vagina. 146 NuevaespeciedelgéneroBerghia DISCUSSION Western Atlantic specimens ofBerghia have been considered to belong to a single and variable species, B. coerulescens (Engel, 1925; Marcus, 1957; Edmunds, 1964, 1966; Marcus, 1976). SinceTardy (1962), someofthe oíd records have been re-exami- ned and assigned toB. verrucicornis. Edmunds (1968) suggested the existence ofsecond western Atlantic species when he compared the specimens from Ghana and re-examined the variable Jamaican material cited as B. coerulescens. He assigned the Ghanaian spe- cimens to B. verrucicornis, and separated the variable material from Jamaica as speci- mens A, B andC. In all three specimens theceras insertionsareconspicuously marked with bright orange, an important character absent in B. verrucicornis (Pl. 1 B). Edmunds (1968) didnotdescribeanew species fromJamaicawhich leadstoconfusión, but suggested two possibilities, either that "it is possible that there is a single West Atlantic species of Berghia which is very variable"or"itis possible thatthere are twoormore speciesofWest Atlantic Berghia, each as distinct as are the two European species". Nevertheless, Thompson (1980) assigned to B. verrucicornis the material from Jamaica and pointed out that "both European species ofBerghia have now been recorded from the Caribbean Figure2. Radularteeth in the speciesofBerghia compared. A. Three median teeth in Berghia rissodominguezi(paratype, MNHN). Scalebar=10um. B. Berghia verrucicornisfrom Asturias (North Spain). Scalebar=10um. C. Berghia verrucicornisfrom Las Palmas (Canary Islands). Scalebar=10um. D. Berghiacoerulescens from Sicily. Scale bar=100 um. Figura2. Dientes radularesen lasespeciesde Berghiacomparadas. A. Three median teeth in Berghia rissodominguezi(paratype, MNHN). Scale bar=10um. B. Berghia verrucicornisfrom Asturias (North Spain). Scalebar=10um. C. Berghia verrucicornisfrom Las Palmas(Canary Is- lands). Scalebar=10um. D. Berghiacoerulescensfrom Sicily. Scale bar=l()() um. 147 Muniainy Ortea Seabut the\ ha\e not been consistently recorded underthe corred ñames". As in otherdes- criptions of Wesl Atlantic specimens, he deseribed the bright orange lines at the ceras msertions, and drew a radula tooth with long and slender denticles. reliable characters present in Berghia rissodominguezin. sp. We examined one specimen from Principe Is- land and. the vermilioncolourtothe rhinophores. the small size and the radularmorphology confirm that it is the same species recorded by EDMUNDS (1968) from Ghana. Principe is the southern point ofdistribution cited for B. verrucicorrúson the eastem Atlantic coast. The main differences between B. rissodomingueziand B. verrucicorrús are: B. risso- domingueziis larger. has conspicuous orange lines at the ceras insertions. white-creamco- lour rhinophore papillae, yellow tips to the tentacles. elongated cerata. a greater number of radular teeth and longer denticles (Fig. 2A. B. C). Berghia rissodominguezi differs fromB. coendescensprincipallyinthecolourpattemandtheradulamorphology(Fig.2A.D). Anotherwestem atlantic species ofBerghia is B. creutzbergiMarcus & Marcus. 1970. in which the radularteeth have altérnate large and small denticles. and there is noorange pigment (EDMUNDS &Just, 1983). which isclearly different fromB. rissodominguezin. sp. From material studied in the present paperwe have transferredthe species SpurUIaco- lumbinaGarcía-Gómez& Thompson,1990tothegenusBerghia. Thisspecieswasdeseribed from the southern Spain (Andalusian coast). extending now to the Canary Islands. Based on evidence from numerous record we can ask. are European species ofBerg- hia present in the Westem Atlantic and are Berghia coendescens and B. verrucicomis really amphiatlantic species ?. Following the authoritative review ofTardy (1962) we considered that B. coendescens was nevercorrectly recorded in reports from the westem Atlantic. Therefore. we suggest that the distribution ofB. coendescens is eastem Atlan- tic (France and northem Spain) and Mediterranean. The westem presence oí\ Berghia ve- rrucicomis is more problematic because some authors mentioned characteristics inter- mediate between B. verrucicomis andB. rissodominguezi (Edmunds. 1968 specimen B). Inconsequence. the valid presenceofB. verrucicomis in the westem Atlantic needs furt- herinvestigation. In azoogeographical discussion Edmunds (1968, 1977) cites 37 speciesofGhanaian opisthobranehs ofwhich 16 oceurin the westem Atlantic, and he maintains Berghia ve- rmciconüsasbeingamphiatlantic initsrange. He suggeststhat the floating tree trunks with coelenterate polyps could easily transpon aeolony ofaeolids across the Atlantic Ocean. Templado etal (1990) included both Berghia coendescens and B. verrucicomis in theirlistofamphiatlantic species.but theyconsideredthat transatlantic dispersal eitheras larvaoron floatingobjeets as unlikely. They conclude that is more probable that the east andwest Atlantic forms are inprocess ofspeciation resultingeitherin twodistinct species orin two populations with sufficientdifferences to merit subspecific rank. The San José Gulf perhaps represents the southern boundary for the subtropical species B. rissodo- Plate 1 (right). Photographsofliving animáisofBerghia. A. Berghiarissodominguezi,Gulfof SanJosé.Chubut. Argentina(Holotype. MNHN). B. Berghiaverrucicomis. BahíadeAlgeciras, Spain. C. Berghiacoendescens. Sicily. Italy. Lámina 1 (derecha). Fotografíasdelosanimalesvivos¿feBerghia. A. Berghiarissodominguezi. GulfofSanJosé. Chubut.Argentina(Holotype. MNHN). B. Berghiaverrucicomis.BahíadeAl- geciras, Spain. C. Berghiacoerulescens.Sicilia. Italia. 148 Nuevaespeciedel géneroBerghia . MuniainyOrtea minguezi,justCape Hatteras is the northernboundary formany othersubtropical marine invertebrates (Berggren & Hollister, 1974, cited in Templadoetal., 1990). ACKNOWLEDGEMENTS WeareverygratefultoDr.AngelValdésforconstmctivecommentsandDr.MalcolmEdmunds forhis critical review ofthe manuscript and the improvement ofthe English. Many people kindly gavespecimensandphotographs(García-Gómez,J. C; Villani,G.;Martínez,E.;Moro,L.;Fernán- dez,X.andCastillo,R.).A.Quintana(MicroscopicalScanningService,UniversidaddeOviedo)as- sistedusinSEMphotos.ThisresearchhasbeensupportedinpartbytheSecretaríadeCienciayTéc- nica (Univ. de laPatagonia SJB, doctoral grant), Fundación Antorchas andConicet through an in- vestigationsubsidyandpostdoctoralfellowshipbytheformerauthor. BIBLIOGRAPHY Cervera,L.&J.C.GarcíaGómez. 1986.MoluscosOpistobranquiosdellitoraloccidentalandaluz:nuevasapor- tacionesfaunísticas.Iberus6: 201-207. Cervera, L.; Templado,J; GarcíaGómez, J. C.; Ballesteros, M.; Ortea,J. A.; GarcÍa, F. J.; Ros,J. & Luque,A. 1988.CatálogoactualizadoycomentadodelosOpistobranquios(Mollusca,Gastropoda)dela PenínsulaIbérica, Baleares yCanarias,con algunasreferencias aCeutay laIslade Alborán. Iberus, su- plemento 1: 1-84. Edmunds,M. 1964.EolidMolluscafromJamaica,withdescriptionsoftwonewgeneraandthreenewspecies. BulletinofMarineSciencefortheGulfandCaribbean, 14: 1-32. Edmunds, M. 1966. Protective mechanisms in the Eolidacea (MolluscaNudibranchia).JournalLinnean So- cietyojhondón,Zoology,47: 27-71. Edmunds, M. 1968. Opisthobranchiate Molluscafrom Ghana. ProceedingsoftheMalacologicalSocietyof hondón, 38: 83-100. Edmunds,M. 1977.Larvaldevelopment,oceaniccurrents,andoriginsoftheOpisthobranchfaunaofGhana.Jour- nalofMoüuscanStudies43: 301-308. Edmunds,M.&Just,H. 1983.EolidnudibranchiateMolluscafromBarbados.JournalofMoüuscanStudies49: 185-203. Engel,H. 1925.WestindischeopisthobranchiateMollusken. 1.Aeolidiadae.Bijdr. Dierk. heiden, 24: 33-80. GarcíaGómez,J.C.&Thompson,T. 1990.NorthAtlanticSpurillidNudibranchs,withadescriptionofanew speciesSpurillacolumbina, fromtheAndalusiancoastofSpain.JournalofMolluscanStudies,56: 323-331. Gosliner,T. 1980.TheSystematicsoftheAeolidacea(Nudibranchia:Mollusca)oftheHawaiianIslands,with descriptionsoftwonewspecies.PacificScience, 33: 31-11 Gosliner, T. 1985. The aeolidnudibranchfamily Aeolidiidae (Gastropoda: Opisthobranchia) fromtropical southernAfrica.AnnalsoftheSouthAfricanMuseum, 95: 233-267. MacFarland,F. 1909.TheopisthobranchiateMolluscaoftheBranner-AgassizExpeditiontoBrazil.helandStan- fordJúniorUniversityPublications,2:1-104. Marcus,Er. 1955. OpisthobranchiafromBrazil.BoletimdaFaculdadedeFilosofía, Cienciasehetras, Uni- versidadedeSaoPaulo,Zoology,20: 89-262. Marcus,Er. 1957.OnOpisthobranchiafromBrazil(2).JournalofthehinneanSocietyofhondón,43:390-486. Marcus,Ev. 1972.OnsomeopisthobranchsfromFlorida.BulletinMarineScience, 22: 284-308. Marcus,Ev. 1976.MarineeuthyneurangastropodsfromBrazil (3).StudiesonNeotropicalFaunaandEnvi- ronment, 11:5-23. Marcus, Ev. 1977. An annotatedchecklistoftheWestern Atlantic warm wateropisthobranchs. Journalof MolluscanStudies,A: 1-23. Marcus,Ev.&Marcus,Er. 1970.OpisthobranchsfromCuraÁaoandfaunisticallyrelatedregions.Studieson theFaunaofCuracaoandotherCaribbeanIslands, 122: 1-129. Ríos,E. 1994.SeashellsofBrazil FundasaoCidadedoRíoGrande. 368pp. 113pl. Rudman, W. 1982. Thetaxonomy andbiology offurtheraeolidacean and arminacean nudibranch molluscs withsymbioticzooxanthellae.ZoologicalJournalofthehinneanSociety,74: 147-196. Tardy,J. 1962. Apropos desespecesdeBerghia (Gasteropodes Nudibranches) descotesde Franceetleur biologie.BulletindelInstituíOceanographique,Monaco,59: 1-20. Templado,J.;Luque,A.&Ortea,J. 1990.Acommentedcheck-listoftheamphiatlanticAscoglossaandNu- dibranchia(Mollusca:Opisthobranchia).AttiCongresoSorrento.havoriS.I.M.Napoli,23: 295-326. Thompson,T. 1980.JamaicanopisthobranchmolluscsII.JournalofMoüuscanStudies, 46:74-99. Trínchese, S. 1877. Descrizione del genere Berghia, Trínchese. Rendiconto delle Sessioni delle Scienze dellIstitutodiBologna, 151-153. 150

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