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New insights into the distribution and biology of some cumaceans (Crustacea: Peracarida) from the Canary Islands PDF

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Preview New insights into the distribution and biology of some cumaceans (Crustacea: Peracarida) from the Canary Islands

Rev.Acad. Canar. Cienc, Vol. XXIV, 29-37 (diciembre de 2012) NEW INSIGHTS INTO THE DISTRIBUTION AND BIOLOGY OF SOME CUMACEANS (CRUSTACEA: PERACARIDA) FROM THE CANARY ISLANDS J. Corbera', R. Riera *, L. Moro' & R. Herrera^ 'CarrerGran,90,08310Argentona.Catalonia, Spain -Centrede InvestigacionesMedioambientalesdelAtlantico(CIMASL) C/ArzobispoEliasYanes.44.38206LaLaguna.Tenerife.Canar\-Islands. Spain *correspondingauthor: rodrigo'^acimacanarias.com 'Ser\iciodeBiodiversidad.ViceconsejeriadeMedioAmbientedelGobiemodeCanarias Edf.UsosMultiplesI,Av.Anagan°35.38071. SCdeTenerife.Canan. Islands. Spain "*Ser\iciodeBiodi\ersidad.ViceconsejeriadeMedioAmbientedelGobiemodeCanarias EdificiodeServiciosMultiplesII(S"*planta). AgustinMillaresCarlo, 18 35071 -LasPalmasdeGranCanada.GranCanada.Canan.'Islands.Spain RESUMEN Se detallan nuevos datos sobre ladistribucionybiologiade algunas especies de cuma- ceosdelas islasCanarias. Campylaspisglabra, Nannastacuscf. ungiculatiisyDiastylisnigosa se citan por primera vez en estas islas. La distribucion de la especie endemica Speleocuma guanche, conocidaiinicamente en la costa surdeTenerife, se amplia araiz de este trabajo a la costanortey oeste de esta. a la \ez que se citaporprimera vez en Gran Canariay Lanzarote. Apartir de los ejemplares recolectados de esta iiltima especie. se ha estudiado su fecundidad estimandose en una media de 11.2 = 2.9 embriones porpuesta. Estos valores son de los mas bajos observados en los cumaceos y se sugiere que son debidos a la vida cavemicola, donde la variabilidad ambiental es inferiory donde existe un menor impacto de la depredacion. Palabras clave: Cumacea. Speleocuma, Iphinoe, Campylaspis, Nannastacus, Dias- nlis, fecundidad. islas Canarias. ABSTRACT New data on the distribution andbiology ofsome cumacean species from the Canarv' Islands are reported. Campylaspisglabra. Nannastacus cf. ungiculatus andDiast}-lis rugosa are first recorded from these islands. The distribution ofthe endemic species Speleocuma guanche, uptonowonly knownfromthe southcoastofTenerife, isextendedto thewestand northcoastofthis islandaswellas it is firstrecorded fromGranCanariaandLanzarotecoasts. Fecundity ofthis species was estimated from the collected specimens, resulting in a mean of 11.9 ± 2.9 embryos perbrood. These values are between the lowest observed in cumaceans, suggestingcavehabitat influencesthatwouldsupport lowerenvironmental variabilityaswell as lowerpredation pressure. Key words: Cumacea, Speleocuma. Iphinoe. Campylaspis. Nannastacus. Diastylis, fecundity, Canary Islands. 29 INTRODUCTION 1. The cumacean fauna ofthe Canary Islands has been scarcely studied. CORBERAet al. [4] compiledachecklistofthespeciesrecordedinwatersofthearchipelago. Thecatalogue includes 29 species, most ofthem inhabiting deep-waterand mainly collected during a 1968 cruiseoftheRRSDiscovery. Later, CORBERAetal. [5] studiedinterstitialcumaceansofCy- modoceameadowsdescribinganewspecies,Iphinoecanariensis, andalmostsimultaneously (CORBERA [3]) described a new genus and species, Speleocumaguanche, dwelling in ma- rine lava caves ofTenerife. Since then, only a few records of/. canariensis have been pub- lished (RIERAe^a/. [15, 16, 17]). Ifthe cumacean faunahasbeenpoorly studied, no information is known aboutthebi- ologyofanycumacean species ofthis archipelago. Early studywas dueto FORSMAN [10], lateron, COREY [6, 7] investigatedthefecundityandreproductivestrategiesofsomespecies. However, while amore or less constantnumber oftaxonomic works has increased the num- berofcurrentlyknown species about 1,600, only a fewhave dealtwith its biology. The study ofthe cumacean material recently collected in different monitoring pro- grammes throughoutthe Canary archipelago allowedto increase the listofcumacean species as well as to extendthe distributionrange ofsome little known species. Additionally, data on thereproductionandfecundityoftheendemic speciesSpeleocumaguanchewasalsoprovided. MATERIALSAND METHODS 2. mm Allspecimenswere sampledbymeansofa0.5 meshsize,wiping Cymodoceano- dosa meadows, and cave walls and roofs (Fig. 1). Samples were deposited in a tray and all V Lanzarote T" 29°N - LaPalma ^ s\ ' ^~V 11' 13 fr ^f 28°N - El Hierro LaGome)ra 't / --' ( '/, fX'aGnraarnia Fuerteventura 1 18°W 16°W 14-W Figure L-Mapofthestudyarea, showingsamplinglocationswherecumaceanswererecorded: L Los Cerebros Cave; 2. Playa San Juan; 3. El Carrizal Cave; 4. Roque Garachico; 5. Punta del Viento; 6. CaveinLosRealejos;7.LasTeresitasBeach;8. MedioAlmudBeach;9. BajadePasitoBlanco; 10. Cave north to El Cabron Beach; \\. Barranco del Kikere; 12. La Catedral Cave; 13. Playa Chica; 14. Se- badalesdeGuasimeta. 30 specimens were collected at the surface because ofthe impoverishment ofaquatic climate (anoxia). In vivo photographs weretaken ofstudiedspecimensandthen they were consened in alcohol 90^ SpecimensofSpeleociimaguancheweremeasured(accuracy±0.025 mm) andthe fe- cundity offemales was estimated by counting intramarsupial contents that were classified into five developmental stages according to BISHOP [1]. Statistics were performed using R v2.13.0 software package (R DEVELOPMENT CORE TEAM [14]). The studied material wasobtainedwithin the frameworkoftheproject MAKARONE- SIA2000, funded by the Organismo Autonomo de Museos y Centros del Cabildo de Tener- ife and "The biota inventory ofmarine ZECS from Tenerife, Gran Canada, La Palma and Lanzarote", funded by the Viceconsejeria de Medio Ambiente del Gobiemo de Canarias (2011). SYSTEMATICS 3. CUMACEA Order Kroyer. 1846 Family BODOTRIIDAE Scott. 1901 Subfamily BODOTRIINAE Scott. 1901 Iphinoecattariensis Corbera, Brito & Nunez. 2001 (Fig. 3 A-C) Studied material.-GranCanaria: Bajade Pasito Blanco, stn 1, UTM438437 3066830.-18 m. 24Au- gust 2011. 1 preadult female: Medio Almud Beach, stn 2, UTM 426611 3075515. -14 m. 24 August 2011. 1 adult male. Tenerife: Las Teresitas Beach, stn 1. UTM 384091 3153903. -7 m. 20 November 2011. 1 adult male. Lanzarote: Sebadales de Guasimeta UTM 638473/3203422.-8 m. 8April 2011, 2 preadult females: Playa Chica, UTM 629884 3199599, sandy unvegetated seabeds. -20 m. 29 April 2012, 1 ind. Distribution.- Iphinoe canariensis was described from southern coast ofTenerife Island on sandy bottoms and Cymodocea meadows between 7 and 16 m depth (CORBER.A.etal. [5]). it was laterreported again in the same area (RIERA etal. [15]) and in a garden eel at deeper bottoms (29.8 m) (RIERAetal. [16]). RIERAetal. [17] reported for the first time the pres- enceofthis species in sandybottoms ofGran Canariaestimatingabundancesupto46 ind m-. Itsdistribution ishereextendedto Lanzarote Islandandnew localities fromGran Canariaand Tenerife are also provided. SubfamilyVAUNTHOMPSONIINAE Sars. 1878 Speleocumaguanche Corbera, 2002 (Fig. 3 D-E) Studied material.- Tenerife: El Carrizal cave, stn 11. UTM 314276/3134470. -6 m. 24 May 2011. 1 aduhmale. 1 ovigerousfemale: LosCerebroscave,stn8.UTM322536/3117655.-10m.22 May2011. 12 preadult females. 17 ovigerous females: Bajade LosRealejos cave, sm 15. UTM 343440 3143984, 31 UTM -37.5 m, 6 June 2011, 1 preadult females, 2 ovigerous females; Punta del Viento, stn 14, 336586/3142697, -5 m, 6 June 2011, 1 preadult female; Roque de Garachico, stn 10, UTM 327359/3140338, -25 m, 24 May 2011, 1 ovigerous female. Gran Canada: cave north to the Cabron Beach, stn7, UTM462456/3083276,-18m,27August2011,2preadultfemales,2ovigerousfemales. Lanzarote: LaCatedral Cave, UTM 629572/3199750,-32 m, 10April 2011, 3 preadult females; Veril de Cagafrecho, in marine caves at different depths (29-39 m) (Puerto del Carmen wrecks UTM 629122/3199850; La Catedral UTM 629751/3199572; Los Camarones UTM 629623/3199631; Bar- rancodel KikereUTM 628543/3199682),numerous individuals, 18-30April2012. Taxonomic remarks.- Although CORBERA [3] included the newly described genus Speleocuma within the subfamily Mancocumatinae Watling, 1977, in a phylogenetic analy- sis ofthe Bodotriidae HAYE [11] foundnot discriminatory characters between the subfami- lies Mancocumatinae and Vaunthopmsoniinae. Consequently, Mancocumatinae was synonymizedwithVaunthopmsoniinae. Regardless,therelationshipofthegenusSpeleocuma with others genera inhabiting noithwestem Atlantic proposed by CORBERA [3] was sup- portedby the phylogenetic analysis (HAYE [11]) that groups inthe same cladeMancocuma Zimmer, 1943, Spilocuma Watling, 1977 andSpeleocuma Corbera, 2002. Biological remarks.- Within the collected specimens, we analyzed 43 ofthem: 1 preadult male, 4 adult males, 16 preadult females and 22 ovigerous. The carapace length is often used in cumaceans as an easily and accurately measured referenceinsteadoftotal length(BISHOP[1], COREY [6]). Anallometricrelationship(Major Axis estimation) betweenthe carapace length (CL) andthe total length (TL) was established (Fig. 2A): TL= 3.8007CLO^^''^ (R- 0.9073; p<0.0001) where the exponent is not significantlydifferentof1 (df=41; p > 0.05) that supports theuse ofthecarapacelengthasreferencemeasurement. Carapacelengthofovigerousfemalesranged from0.725 to 0.9mmwithameanvalueof0.823 ±0.043 mm. Theirfecundity(F) fluctuated between6 and 18 individualspermarsupium,withameanvalue of11.2±2.9 individualsper marsupium.Thereisasignificantpositivecorrelationbetweenthisfecundityandthecarapace length (CLinmm) ofthe adult females, butthe coefficient ofdetermination R^ value is very low (Fig. 2B), meaning that less than 35% ofthe variation in the fecundity can be explained by carapace length. Within the ovigerous females the following stages ofdevelopment were found: stage I, 18.8%; stage II, 31.3%; stage III, 25%; stage IV 12.5%; stageV, 25%. The diameterofel- lipsoideggs/embryos (stage I) fluctuatedbetween0.175 and0.275 mmwith ameanvalue of 0.223 ± 0.026 mm and a mean volume of0.004 ml The simultaneous presence oftwo suc- cessive stages (IV-V) in two ofthe examined marsupium suggests that development ofS. guanche maybe occasionally asynchronous. Fecundity ofS. guanche is one ofthe lowestwithin those ofcumacean species so far known(seeCOREY[6, 7],JOHNSONetal. [13]). Onlythedeep-waterspeciesLeuconjonesi Bishop, 1982 and the summer generation ofAlmyracumaproximocull Jones and Burbanck, 1959,inhabitingintertidalfreshwatersprings,havealowermeanfecundity(8.8 and6embryos perbrood respectively; BISHOP [1], DUNCAN [8]). However, while mean carapace length forthe summergenerationofA.proximoculiis smallerthanofS. guanche, inL.jonesiiscon- 32 OO B ° TOLf==R3-418=0P09<700C7L03-0"0"1 iiE. dfR=-18=.0P3=3064007 S . TEO 2 - o /Xy 0Q). oy o ~1- o ^^^/^/^o o O o o y^ aj *"* ^^^ ^^ 1c -^^^^ o o UL ® - ° opreadultfemales ^ o Aadultmales ^preadultmales «3 - 0.70 0.75 080 0.85 0.90 CL(mm) CL(mm) Figure2.-Speleocumagiiancherelationships between carapace length (CL) and total length (TL)(A and betweencarapace length and fecundity (F) (B). siderablybigger(mean 1.03 mm; BISHOP [1], 1982). Ontheotherhand,Pseudociima longi- corne(Bate, 1858)thathasasimilarcarapace length(0.85 mm), has ahigherfecundity(mean 20.9 embryos per brood; COREY [7]). Although there is a relation between the carapace length (i.e. the size ofthe female) and the fecundity, COREY [7] pointed out that shallow water cumaceans has larger broods that ofinhabiting deep sea in order to offset higher pre- dationaswell astocompensate instabilityoftheenvironment. Submarinecaves, likethedeep sea, could act as a protective habitat, thus fa\ouring a lower fecundity that at the same time may imply a lowerenergetic cost. Distribution.- Speleocuma giianche was only known from the cave system ofthe type lo- calityon the southeasterncoastofTenerife (CORBERA[3]). Itsdistribution ishere extended tothewestandthe north coastofthis islandand alsotothe south coasts ofGran Canaria and Lanzarote. FamilyNANNASTACIDAE Bate, 1866 Campylaspisgiabra Sars. 1879 (Fig. 4 A-B) Studied material.- Tenerife: El Carrizal cave, stn 11. UTM 314276'3134470. -6 m. 24 May 2011. 1 preadultfemale.GranCanaria: cavenorthtoElCabron Beach,stn7.UTM462456 3083276.-18m.27 August2011, 1 preaduhmale. m Distribution.- Campykispis glabra is an eurybathic species recorded from 15 to 3,000 depth and widely distributed in the north Atlantic Ocean and the Mediterranean Sea. FAGE [9] reported this species from deep waters offthe coast ofSenegal (eastAfrica), but it is here recorded for fist time from shallow-water submarine ca\'es ofthe Canarv Islands. 33 Nannastacus cf. ungiculatus (Bate, 1859) Studied material.- Tenerife: Playa San Juan, stn. 6, UTM, 3118099/322029, -15 m, 20 July 2011, 1 ovigerous female. Distribution.- This species is known fromthe northeastAtlantic, the Mediterranean andthe Black Sea. ItinhabitsamongphotophilicalgaeandinPosidoniameadowsofshallowbottoms m between and 40 depth. Although it has been recorder at deeper bottoms (110-120 m; LEDOYER [12]), the study ofthat material deposited in the MNHN-Paris confirmed that it actually belongs to A^. atlanticus [see Supporting information File S2 pp 238-247, in COLL etal. [2]]. PAGE [9] reportedthis species fromtheAtlantic coastofMorocco. Itsdistribution is here extendedto the Canary Islands. Family DIASTYLIDAE Bate, 1856 Diastylis rugosa Sars, 1865 (Lam. 4 C-D) Studied material.- Lanzarote, Puerto del Carmen, cueva de La Catedral, UTM 629751/3199572,-32 m, 29April 2012, 2 specimens. Distribution.-Diastylisrugosa has a depthrange from to 90 m, where itinhabitsandyand muddy sand seabeds ofthe upper shelf. This species is widely distributed in the Northeast Altantic Ocean(fromNorwayto the BayofBiscay) andthe Mediterranean Sea. Here, itsAt- lantic distribution is extended south to the Canary Islands. ACKNOWLEDGEMENTS 4. To Rafael Herrero (AquaWork Producciones) for diving assistance in Tenerife, Lan- zaroteandGranCanada.WeacknowledgePatriciaMonagas,NinoNavarroandAndreaCasini fortheircollaborationduringfieldcampaigns. ToJuanaAbadCelliniandLeopoldoMoroGar- cia,EmilioRodriguez(Hippocampus-FarionesDiveCenter),AlfonsoMontesdeOca(Naosub Dive Center) for logistic support. To Eva Ramos (CIMASL) forproviding the studied speci- men belonging to the genus Nannastacus. And last but not least, to Dr. Juan Jose Bacallado Aranega (Directorofthe Project MAKARONESIA2000) forhis continuous encouragement. REFERENCES 5. [1] BISHOP, J.D.D. 1982. The growth, development and reproduction of a deep sea cumacean (Crustacea: Peracarida). ZoologicalJournal ofthe Linnean Society, 74(4): 359-380. [2] COLL, M., PIRODDI C, STEENBEEKJ., KASCHNERK., BEN RAIS LASRAM F., etal. 2010. TheBiodiversityoftheMediterranean Sea: Estimates, Patterns, andThreats. PLoS ONE 5(8): el1842. 34 [3] CORBERA, J. 2002. Amphi-Atlantic distribution ofthe Mancocumatinae (Cumacea: Bodotriidae), with description ofa new genusdwelling in marine lavacavesofTenerife (Canary Islands). ZoologicalJournaloftheLinnean Society^ 134(4): 453-461. [4] CORBERA, J., BRITO, M., NUNEZ,J. and RIERAR. 2001. Catalogode loscumaceos (Crustacea, Malacostraca)de las IslasCanarias.RevistadelaAcademia CanariadeCien- cias, 12(3-4): 67-73. [5] CORBERA, J., BRITO, M. andNUNEZ,J. 2002. Interstitial cumaceans from sandy bot- toms and Cvnwdocea meadows ofthe Canary Islands. Ca/uers de Biologie Marine, 43(1): 63-7i. [6] COREY, S. 1969. The comparative life historv' ofthree Cumacea (Crustacea): Ciimop- sisgoodsir (van Beneden). Iphinoe trispinosa (Goodsir). and Pseudocuma longicornis (Bate). CanadianJournalofZoology, 47: 695-704. [7] COREY. S. 1981. Comparati\efecundityand reproducti\estrategies in seventeen species ofthe Cumacea (Crustacea: Peracarida). Marine Biology. 62(1): 65-72. [8] DUNCAN, T.K. 1984. Life history ofAlmyracumaproximoculi Jones and Burbanck. 1959 (Crustacea: Cumacea) from intertidal fresh-watersprings on Cap Cod, Massachu- setts. JournalofCrustacean Biology, 4(3): 356-374. [9] PAGE, L. 1932. Larepartition des Cumaces dans les zones profonde et cotiere de LEst- Atlantique. Soixante-cinquieme Congres des Societes Savants, 205-208. [10] FORSMAN, B. 1938. Untersuchungen liber die Cumaceen des Skageraks. Zoologiska Bidragfran Uppsala, 18: 1-161. [11] HAYE, RA. 2007. Systematics ofthe genera ofBodotriidae (Crustacea: Cumacea). Zo- ologicalJournaloftheLinnean Society, 151(1): 1-58. [12] LEDOYER, M. 1983 Contributiona I'etudede Lecologiede la faunevagileprofondede la Mediterranee nord-occidentale. II: Les cumaces (Crustacea). Tethys 11(1): 67-81. [13] JOHNSON, W., STEVENS, M. and WATLING, L. 2001. Reproduction and develop- ment ofmarine peracaridans. Advances in MarineBiology, 39: 105-260. [14] R DEVELOPMENT CORE TEAM 2011. R:A Language andEnvironmentforStatisti- cal Computing. R Foundation for Statistical Computing, Vienna, Austria. ISBN 3- 900051-07-0. [15] RIERA, R., RODRIGUEZ, M. and MONTERROSO, O. 2011. Macroinfaunal assem- blages in sandy seabeds ofSan Bias (SE Tenerife, Canary Islands. NEAtlantic Ocean). Vieraea, 39: 65-76. [16] RIERA, R., DELGADO. J.. RODRIGUEZ, M., MONTERROSO. O. and R.'XMOS, E. 2012a. Macrofaunal communities ofthreatened subtidal niaerl seabeds onTenerife (Ca- nary Islands, north-east Atlantic Ocean) in summer. Acta Oceanologica Sinica, 31(1): 98-105. [17] RIERA, R.,TUYA, P., RAMOS, E., RODRIGUEZ, M. andMONTERROSO, 6. 2012b. Variability ofmacrofaunal assemblages on the surroundings ofa brine disposal. Desali- nation, 291: 94-100. 35 Figure3.-A-C.IphinoecanahensisCorbera,Brito&Nunez,2002: adultmalefromTenerife(A-B)and preadultfemalefromGranCanada(C);D-E.SpeleocumaguancheCorbera,2002: individual fromLan- zarote(D)andpreadultfemalefromTenerife(E). 36 Figure4.- A-B. Campylaspisglabra Sars. 1879: preadult female from Tenerife (A) andpreadult male from Gran Canaria (B): C-D.Diasnlis fu^osa Sars. 1865 from Lanzarote. 37

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