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Cuticular structures on the labium of the larva of Crocothemis servilia (Drury) (Anisoptera: Libellulidae) PDF

5 Pages·1992·0.84 MB·English
by  GuptaA
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Preview Cuticular structures on the labium of the larva of Crocothemis servilia (Drury) (Anisoptera: Libellulidae)

Odonalologica21(1): 97-101 March I. 1992 Cuticular structures on the labiumof the larva ofCrocothemis servilia (Drury) (Anisoptera: Libellulidae) A. Gupta¹,S.Dey²,S.Gupta² 1 DepartmentofZoology, St.Edmund’s College,Shillong-793003,India 2 Electron MicroscopeLaboratory, RegionalSophisticatedInstrumentationCentre, North-Eastern HillUniversity, BijniComplex,Shillong-793003, India Received September24, 1990/ Revised andAcceptedNovember 12, 1991 The various types ofsensilla occurringon the labium aredescribed with the help ofscanningelectron microscopy. In addition tobristles andspines, various sensilla trichoidea are located on the ligulaand the palps. Thepalps also contain sensilla basiconica, arow ofpapillaeand simplepits. Thepossiblefunctional roles playedby these types ofsensillum in the life ofC.serviliaare discussed. INTRODUCTION Scanning electronmicroscopyofthecuticularstructures foundontheappenda- ges and body surface of aquatic insects has extended our knowledge ofthe structure ofanumberoftypesofsensillum(GOUTEAUX, 1977;SLIFER, 1977; DAHL, 1978; LEE & CRAIG, 1983; KAPOOR, 1985a, 1985b; WOLFE & ZIMMERMAN,1984).Thepresentstudy describestheexternal sensory receptors on the labiumofthelarval Crocothemisservilia. Thelabiumis consideredto be a very important structure inodonate larvae. Itis foldedupon itselfandtucked beneath the head ventrally. Itis used to capture prey organisms by thrusting it forward. Therefore, ascanning electron microscopic examinationofthevarious types ofsensillumpresenton it is likely to provide abasis forunderstanding the relationship betweenthe morphology ofthe larvaeand their significant role as predators. Furthermore, as the bristles and other structures on the labium are extensively usedin differentiatinggeneraandspecies inthelarvalstage,adetailed knowledge of labialstructures is likely to be important frojn ataxonomic point of view. 98 A.Gupta, S, Dey &S. Gupta MATERIALANDMETHODS Crocothemis servilia inhabits the pondsof Shillongand itsneighbouringareas (lat.25° 34’N; long.90°52’E)inthenorth-eastern regionofIndia.Larvaewerecollected fromWardlake,aperennial lentic waterbodyinShillong,fromthemarginalweedbeds.Thelabiumwasfixedin 2.5%glutaralde- hyde in 0.1 Msodium cacodylatebuffer for 2-4 hours. This was followed by washing in buffer, post-fixationin 1%osmium tetroxide, dehydrationin gradedconcentrations ofacetoneand drying (WOOLLEY& VOSSBRINCK, 1977).Itwassecured tobrass stubsbyanelectro-conductive paint, ’Dotite’. This was followed by coatingwith athin layerof goldina Fine Coat Ion SputterJFC 1100. They wereexaminedin aJSM-35 scanningelectron microscopeoperatedat 15 KV. RESULTS InOdonata,the labiumis foldeduponitselfataboutits midlength andturned backward. In C.servilia, thelabiumhas well-developed premental setae,which are bristlesor sensilla chaetica. Thefront marginoftheprementum is produced intoatriangular ligula. Thehinged palps arearmed withtwo curvedhooks.The palpal margin is beset with bristles and other sensilla (Fig. 1). The premental setae are arranged ina group,somewhat like abristle-field, each setaemerging from aroughly conical socket. The basalregion ofboth the ligula andthepalps bear sensilla trichoidea, designated here as type 1, 28-57 pm long, each with a bulb-shaped socket and arelatively stout basal region tapering sharply towards the apex (Fig. 2). Similartrichoid sensilla, 20-33 pm long are also strewn on the central and apical regions ofthe ligula. Interspersed among them are a few sensilla trichoideaof type la, around 80 pm long. These have similar sockets to thoseoftype 1,butare more slenderand whip like(Fig.3). Sensillatrichoidea designated type 2 are arranged atregular intervals along thefrontmargin ofthe ligula, forming a definitepattern. They are 33-60pm long and emerge from circular punctures fringed with collar-like structures. Their tips are relatively blunt (Fig. 3). The proximal outer margin of the palps is beset with a row of long (about 580 pm) bristles with heavily sclerotizedbases. A few shorter but sharp-tipped spines canalsobe seen (Fig. 4). Thefront andinnermargins ofthe palps containarow ofsensilla trichoideatype2a, having similarsockets tothose of type 2 found on the ligular margin, but with relatively pointed tips. Their length gradually diminishesfromabout 100pm inthecentre toabout30 pmon thesides. Beyond them, almost along theedge, is alinearrow ofpapillae (Fig. 5). At higher magnification, each type2a trichoidsensillum can beobserved to be associated with a pit about6 pm in diameter. Each papilla has three lips, diminishing in size from the innerto theouter. On one side ofeach papilla is a short (3-5 pm) basiconic peg and, onthe other side, a still shorter (1-1.5 pm) basiconic peg;these are designated as types 1 and la respectively (Fig. 6). Type 1 basiconic pegsarealso strewn overthesurfaceofthe palps withtype 1 sensilla trichoidea(10-23 pm long) interspersed amongthem(Fig. 7). Larval labium ofCrocothemisservilia (Dru.) 99 Figs 1-7.Crocothemis servilia,cuticular structuresonlarval labium: (1)Labium,generalview;(2) Prementalsetae, magnified;(3)Ligulashowingsensilla; (4)Bristles and spinesonthe outer margin ofthepalp;(5)Sensilla onthe frontmarginofthepalp;(6) ditto,magnified;(7)Surfaceofthepalm withsensilla basiconica and sensilla trichoidea. [Ig: ligula;pm: prementum; pms: prementalsetae; pi:palp; br: bristles;s:spines; p: papillae;l.p: lipsofpapillae;t 1: sensilla trichoidae, type 1;t la: ditto type la; t 2:ditto, type2; t 2a: ditto, type2a;bl: sensilla basiconica,type 1;bla: ditto, type la.Allthe barsare 100pm except those inFigs. 1and6, whichare 1000pm and 10pmresp.] DISCUSSION Scanning electron microscopy, because ofits large depth offield and high resolvingpowerbecomes indispensablefordetailedmorphologyofinsectsensilla (SCHMIDT& SMITH, 1987). Basedon theheterogeneity, complexity andabundanceofsensilla, the labium appears to be a very important sensory region ofthe head. This is in keeping 100 A.Gupta, S.Dey & S.Gupta with itsfunctionsofcapturingandsampling theprey.Thebasiconicpegsassocia- ted withthe lineararrayof papillae on the margins of the palps are likely to be chemoreceptors, as concludedby AMRINE & LEWIS (1978, 1986) for similar sensory structures foundin the fleaCediopsylla simplex. Theligular andpalpal surfaces are clothedin sensilla trichoideaofafew types. These are presumably all mechanoreceptors. However, the longer, more slender ones (type la) could also possibly detect the presence ofanother object withoutcoming intoactual contact with it. This would be possible due to a force on the insect caused by the increased drag as it passes an object, or vice verse. Thus any object within 10to 100 diametersofthe insect would be readily detected due to a wave of resistancewhichwouldbereflectedbackagainsttheinsect(WOLFE& ZIMMER- MAN, 1984). Thereforeit appears that C. servilia, which is known to be an efficient predator ofother insects and fish spawn, couldbank upon its array of sensilla tolocate andambushitsprey.Thepremental setae are grouped together intheformofabristlefield, andprobably functionas proprioceptors in addition toproviding usefultactileinformationtothenymphs (AMRINE&LEWIS, 1978, 1986; SCHMIDT & SMITH, 1987).Thus they are likely to be instrumental in providing feed-backinformationaboutthestretchingofthe palps duringpreycap- ture. The functional significance ofthe numerous pores on the palps cannot be ascertainedat present. AMRINE &LEWIS (1978, 1986) suggested that similar pores found in the flea Cediopsylla simplex are openings to epidermal glands which secrete anoily substance. However, theirrole inaquatic larval stages can only be determinedthrough studiesonfinestructure, innervationandphysiology. Finally, the occurrence, density and arrangement of the labial sensilla are expected to serve as usefulmorphotaxonomic charactersinspecies differentiation. ACKNOWLEDGEMENT We thank Dr D.T. KATHING, Head, RegionalSophisticatedInstrumentationCentre, Shillong, India,forhis help and encouragement. REFERENCES AMRINE, J.W.& R.E. LEWIS, 1978. The topographyoftheexoskeleton ofCediopsyllasimplex (Baker1895)(Siphonaptera:Pulicidae). I.Theheadanditsappendages.J.Parasitol. 64:343- 358. AMRINE, J.W.& R.E.LEWIS, 1986. The topographyofthe exoskeleton ofCediopsyllasimplex (Siphonaptera:Pulicidae):thethorax, abdomen andappendages,J.Parasitol. 77; 71-87. DAHL, C., 1978. Scanning electron microscopicstudies ofepicuticularpattem in mosquito larvae (Diptera,Culicidae) andtheiruseastaxonomic characters. Zoologicascripta7:209-217. COUTEAUX,J.P., 1977. Micromorphologyofthelarval andnymphalcuticleofSimulium (Diptera: Simuliidae)ofZaire, near orincluded in the Simulium damnosum complex. Tropomed. Parasitol. 28: 97-99. Larval labiumofCrocothemis sen’ilia (Dru.) 101 KAPOOR,N.N., 1985a.Electron microscopicstudy ofcuticular and cellular structures ofthebody surface of the winter stonefly nymph.Taeniopteryx burksi Ricker and Ross (Plecoptera: Taeniopterygidae).Can. J.Zoo!. 63: 1360-1367. KAPOOR,N.N., 1985b,Externalmorphologyanddistribution oftheantennalsensillaofthestonefly, Paragnetinamedia (Plecoptera: Perlidae).Int.J.Insect Morph.Emhryol. 14:273-280. LEE, R.M.K.W. & D.A. CRAIG, 1983. The labrumand labral sensilla ofmosquitoes (Diptera: Culicidae) : Ascanning electronmicroscopestudy. Can. J. Zoo/.61: 1568-1579. SCHMIDT, J.M. &J.J.B.SMITH, 1987. Theexternal sensory morphologyofthe legs and hairplate systemoffemaleTrichogrammaminutumRiley (Hymenoptera: Trichogrammatidae).Proc. R. Soc. Land. (B)232:323-366. SLIFER.E.H., 1977.Senseorgans ontheantennalflagellumofmayflies(Ephemeroptera).J.Morph. 153: 355-362. WOLFE,G.W. & J.R. ZIMMERMAN, 1984. Sensilla, punctation,reticulation, andbody shapein the Hydroporinae(Coleoptera: Dytiscidae).Ini. J.Insect Morph.Emhryol. 13: 373-378. WOOLLEY,T.A.&C.R.VOSSBRINCK, 1977. Scanningelectron microscopy asatool inarthropod taxonomy, pp. 645-652. In: SEM/1977/1IT Research Institute,Chicago, II.

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