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Description of the last larval instar of Epophthalmia vittata cyanocephala Hagen, 1867 (Anisoptera: Corduliidae) PDF

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by  BedjaničM
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Preview Description of the last larval instar of Epophthalmia vittata cyanocephala Hagen, 1867 (Anisoptera: Corduliidae)

Odonatologica29(1): 57-61 March 1.2000 Description of thelast larval instar of Epophthalmia vittata cyanocephala Hagen, 1867 (Anisoptera: Corduliidae)* M. Bedjanič Fram 117/a,SI-2313 Fram, Slovenia Received May 19,1999/RevisedandAcceptedAugust4, 1999 The ultimate instar larva is described and figuredfrom exuviae, collected near Anuradhapura,Sri Lanka. Our present knowledgeofthe larval forms ofthe genus is briefly discussed. INTRODUCTION The genusEpophthalmia Burmeister comprises the eleventaxa ofwhich E. biosdinataLewis, 1969isknown only from afossilrecord while otherten mem- bers are distributedthroughout southern and eastern Asia (Tab. I). Although the representatives ofthegenusEpophthalmia are very large andconspicuous insects, they are ratherpoorly represented incollectionsand some ofthem arevery inad- equately known. This is particularly true forthe larval stages towhich very little attentionhas beendevotedinthepast. They are characterizedby very long legs, a smallrectangular headwithtwolatero-posterior projections andsmallpointed eyes as wellas by abroadly ovalabdomenwithstrongdorsal spines. Of special interest, however,is theverybig andspecialized labiumwithpeculiarly shaped labialpalps, which appears tobe unique inthewholefamily Corduliidae. In the detailedrevision ofthe genusEpophthalmia, produced by L1EFTINCK (1931), the authoralso summarized all published information on the larval features of representatives ofthat genus and described the last larval instars of three species, viz. E. elegans, E. vittigera and E. vittata vittata. Apart from E. elegans whichhas been studied indetail andis well known (ISHIDA, 1996), the two other descriptions are based on very limited numbers of larvae or *Dedicated to ProfessorDrGerhardJURZITZA,ontheoccasion ofhis70lhbirthday. 58 M. Bedjanic exuviae, which were not rearedto metamorphosis or taken during emergence. Also in Epophthalmia vittata cyanocephala, which is endemic to Sri Lanka, larval stages and exuviae have not been described previously. Unfortunately, the present description is based on a single larval skin, without definite association with the adult stage. According to the fact that the subspecies is confinedto Sri Lanka and at the same timeis the only representative of the genus on the island the determination is not doubtful, yet it makes any comparison and differential analysis with other taxa almost impossible. Table I Extant representatives ofthe genus Epophthalmiawith their known distribution range — [Taxa in which last larvalinstars havebeen describedareasterisked[ SSppeecciieess DDiissttrriibbuuttiioonn aauussttrraalliiss HHaaggeenn,, 11886677 IInnddoonneessiiaa ((CCeelleebbeess,, MMaalluukkuu)) ** ee..eelleeggaannss((BBrraauueerr,, 11886655)) CChhiinnaa,, JJaappaann,.HHoonnggKKoonngg,.TTaaiiwwaann ee..yyaaggaassaakkiiiiEEddaa,, 11998866 NNoorrtthhKKoorreeaa f/..frforonnttaalliiss SSeellyyss,, 11887711 IInnddiiaa((AAssssaamm,,wweesstteerrnnHHiimmaallaayyaa)),,TThhaaiillaanndd,,MMaallaayyssiiaa ff..bbiinnoocceellllaattaa((FFrraasseerr,, 11992244)) IInnddiiaa((WWeesstteerrnnGGhhaattss)) ** vviittttaattaa vviittttaatlaaBBuurrmmeeiisstteerr,, 11883399 IInnddiiaa((PPeenniinnssuulalarrIInnddiiaa.,UUttttaarrPPrraaddeesshh,, WWeessttBBeennggaall)) ** vv..ccyyaannoocceepphhaallaa HHaaggeenn,, 11886677 SSrriiLLaannkkaa vv..ssuunnddaannaa LLiieeffttiinncckk,, 11993311 IInnddoonneessiiaa((eeaasstteerrnnSSuummaattrraa,,WWeesstt&&CCeennttrraall JJaavvaa)),,VViieettnnaamm ** vviittttiiggeerraavviittttiiggeerraa((RRaammbbuurr,, 11884422)) IInnddoonneessiiaa((BBaannggkkaa,, BBiilllliittoonn,, JJaavvaa,, BBaallii,, BBoorrnneeoo)),,MMaallaayyssiiaa,, SSiinnggaappuurr,,tthhee PPhhiilliippppiinneess vv.. bbeelllliiccoossaaLLiieeffttiinncckk,, 11994488 IInnddiiaa((eeaasstteerrnnIInnddiiaa)),,MMyyaannmmaarr((BBuurrmmaa)),,TThhaaiillaanndd,,VViieettnnaamm DESCRIPTION Material.— 1ex.(6);Watertank700mSEoftheAbhayagiriDagoba,Anuradhapura,Anuradhapura District, NorthernCentral Province,SriLanka, 19-1-1995, alt. 100m;M.BedjaniCleg.& det.Material is depositedinauthor’sprivate collection. Head. — In general appearance it agrees well with the detaileddescription provided by LIEFTINCK (1931). Eyes in the latero-anteriorcomer ofthe head smallandprominent, directed upwards. Twoprojections on dorsallatero-posterior part directedbackwards, following theimaginary diagonal to the eye onopposite side ofthehead. On the lateralsurface, belowtheprojection, two fields ofsmall thinsetae. Betweenbasesofantennae ashortmedianprocess thatreaches themid- dleoffirst antennaljoints. Anteriorpart prominent, gradually flattenedtowards posterioredge, whichends attheanteriorpartofocelli.Prominentanteriorpartof medianprocess semicircular, flattenedfrontally, with dorsaledge slightly thicker. Withthe exception offirst segmentsantennae broken. Labium very big, with peculiarly shaped labial palps (Fig. 1). Viewing laterally, mask very flattened with labial palps curved upright following the Larva ofEpophthalmiavittata cyanocephala 59 shape of the head. The articulation between prementum and postmentum reaches distally the middle of metathoracic poststernite and coxae of metathoracic legs respectively. Labial palps and prementum (basal part and articulationprementum-postmentumnot indicated) are shown in Figure 1. On the left labialpalp fourth hook the longest, sixth the shortest and on theright labial palp fifth hook the longest, first three hooks being the shortest. Apical halves ofhooks black. Legs. — Very long, coxae ofprothoracic legs and apical halfof coxaeof mesothoracic legs overgrown with longer hair-like setae, coxae ofmetathoracic legs sparsely overgrown withshortersetae. Lateraledges ofthoracicbasisternites withtuftsoflong hair-like setae. Abdomen. — Very large, oblonge, abdominalsegments S5-S7the broadest. VentralsurfaceofabdominalsegmentsS1-S8very poorly setose,posterioredge of S9withgenerally sparselongerhair-likesetae,whichare thelongest onthelateral fringeandreach halfof S10in length. Ventral surface of S10laterally overgrown withvery shortsetae,whichcover alsothe ventralsurface ofparaprocts,between whichlong hair-like setae outgrow. Dorsal surfaceofabdomenin surrounding of mid-dorsalhooks andposterior edges ofsegments overgrown with very small spiniform setae. Lateral margins ofabdomenovergrown with short strong setae. Between these, on abdominal segments S6-S9, much longer hair-like setae out- grow,being mostbushy apically. Mid-dorsalhooks onsegments S4(?)-S9, S3 with only small pointed protuberance, lateralspines on segments S8-S9(Figs 2 and 3). Analpyramid atriflelonger thanabdominalsegmentS10,paraprocts being thelong- Figs 1-3.EpophthalmiavittatacyanocephalaHagen,larval structural features: (1) prementum (with- outbasalpart) and labial palps,dorsal view; —(2) abdomen,dorsalview; — (3)abdomen,left lateral view (dorsal spine(?)onabdominal segment S4broken). 60 M.BedjaniC est, epiproct little shorter, cercithe shortest but almost as long as epiproct (Fig. 3). Measurements (mm).— Body length: 31.5;abdomen length:21.5; abdomen width: 13.1; lengthof 10th. abdominalsegmentinch analpyramid:2.9;tibia length(prothoracic,mesothoracic & metathoracic leg):8.2,9.9, 13.0; femurlength(metathoracicleg): 12.2;labiumlength:9.9;prementum length:6.1;prementum width: 5.3; moveable hook length: 1.0;lengthoflatero-posteriorhead-projec- tions: 0.7. DISCUSSION Larvalformsoftherepresentatives ofgenusEpophthalmia areverypoorly known. According toLIEFTINCK(1931) theknownlastlarvalinstarsarerathersimilarin somecharacters, however,as already statedby himself, alittledoubtremainsas to thecorrectness of descriptions since material usedin his study was not reared or taken during emergence.In view ofourpresent knowledge on thedistributionof Epophthalmia species thereare actually some problems. The description ofE. v. vittatabasedon asingle larvacollected nearCalcuttainIndia, mayreferratherto E. vittigerabellicosa, whichalsooccurs inthatregionandwas described later. Itis also uncertainwhether description oflast larval instarofE.frontalis (FRASER, 1919) was correctly ascribedto E. v. vittataby LIEFTINCK (1931) and FRASER (1936). Bothauthorsoverlookedinformationonthenumberof dorsal spines given inFraser’s description, whichare statedtobe onthefifth toninthabdominalseg- ments,whileinthe description of E. v. vittataLIEFTINCK(1931)dorsalspines in this species are on thefourth to ninthabdominalsegment. The speculation that FRASER(1919) actually describedthelastlarvalinstarofE.frontalisbinocellata is thereforealso possible. Although itisalmostimpossible andnotveryreasonabletomakeconclusionson thebasisofsingle exuviae, there are someclear differencesbetween E. v. vittata and E. vittata cyanocephala in the shape of the labial palps. In E. vittata cyanocephala, the very long fourthand very shortsixth hooks ofthe left labial palp are specific andshow cleardifferenceincomparison withE. v. vittatainwhich fifthand sixthhooks onthe left labialpalp arethe longest (LIEFTINCK, 1931). It can be immediately separated from E. elegans by the absenceofthewell devel- oped dorsalspine onthethirdabdominalsegment(ISHIDA, 1996).Usefulcharac- ters for distinguishing E. vittatacyanocephala fromE. v. vittigeraare diffentshape of the labialpalps, the smaller latero-posterior head-projections and different shape ofthe short median process between the bases of antennae. When the shape of labial palps is concerned, it is worth mentioning that a study of a dozenexuviae of E. v. vittigera, collected at RiamKannan Lake in Borneo, revealedindividual deviation in theform ofthe labial palps, the shape ofthe leftand right sides in some specimens being reversed. Forthe analysis ofotherdifferentialfeaturesmuchmorematerialis needed,not only inE. vittatacyanocephala, butespecially inthespecies with stillundescribed Larva ofEpophthalmiavittatacyanocephala 61 last larval instars. Only then will a competent revision ofthe larval forms in the genusEpophthalmia be possible. REFERENCES BEDJANlC,M., 1998.Anattemptoftheanalysisofthe odonatefaunaofSriLanka(Insecta:Odonata). Graduationthesis. DeptBiol., Univ. Ljubljana. BRIDGES, C.A., 1994. Catalogueofthefamily-group,genus-groupandspecies-groupnamesofthe Odonata ofthe world. 3rd edn,Bridges, Urbana, Illinois. EDA,S., 1986. ArecordofOdonata from Pyongyang,Korea, withdescriptionofanewsubspecies of Epophthalmiaelegans. Tombo 29(3/4):60-65. FRASER, EC., 1919. Descriptions ofnew Indian odonate larvae and exuviae. Rec. IndianMus. (B) 16(7):459-467,pis 32-37 excl. FRASER, F.C., 1924. Asurvey ofthe Odonata(dragonfly)faunaofwesternIndiawithspecialremarks onthe genera Macromia and Idionyxand descriptionsofthirtynewspecies.Rec. IndianMus. 26: 423-522,3pis excl. FRASER, F.C., 1936. ThefaunaofBritishIndiaincludingBurmaandCeylon,Odonata,Vol.3.Francis &Taylor,London. ISHIDA,K„ 1996. MonographofOdonata larvae inJapan.Hokkaido Univ. Press, Sapporo. LIEFTINCK,M.A., 1931.A revision ofthe genus EpophthalmiaBurnt. (Odon., Corduliinae),with notes onhabits and larvae. Treubia 13(1);21-80,pi. 1excl. LIEFTINCK,M.A., 1948. Entomologicalrecords fromthe Swedish Expedition 1934 toBurma and British India.Ark. Zool. 41(A): 1-23.

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