ebook img

New species of Actinote (Hubner (Nymphalidae: Acraeinae) from southeastern Brazil PDF

12 Pages·1996·6.5 MB·English
Save to my drive
Quick download
Download
Most books are stored in the elastic cloud where traffic is expensive. For this reason, we have a limit on daily download.

Preview New species of Actinote (Hubner (Nymphalidae: Acraeinae) from southeastern Brazil

JournaloftheLepidopterists'Society 50(4), 1996,309-320 NEW SPECIES OF ACTINOTE HUBNER (NYMPHALIDAE: ACRAEINAE) FROM SOUTHEASTERN BRAZIL Carla M. Penz1 DepartmentofZoology, UniversityofTexas, Austin,Texas 78712, USA AND RONALDO B. FRANCINI MuseudeZoologiada Universidade de SaoPaulo, C.R 7172 Sao Paulo, SP01064-970, Brasil ABSTRACT. Three newspecies ofActinote (Acraeinae) from southeastern and south- ern Brazilaredescribed:Actinote dalmeidai,A. catarina andA. bonita. Diagnosesand illustrationsareprovidedforthenewspecies andforthepreviouslydescribedA. alalia,A. conspicua,A. surima, andA. quadra. Additional keywords.Actinotedalmeidai,A. catarina,A. bonita, mimicry. Butterflies ofthe genus Actinote Hiibner (Acraeinae) are well known for their involvement in Miillerian mimicry complexes (Brown & Ben- son 1974, Francini 1989, Brown & Francini 1990) and for their intra- specific variation in wing coloration and pattern. These two features ac- count for the large number of varieties, subspecies, and species that have been described since the beginning ofthis century. The species described herein belong to the "orangish red mimicry complex" ofFrancini (1989) and the "alalia mimicry complex" ofBrown and Francini (1990), both of which include the deep orange colored Actinote alalia (Felder), A. conspicua (Jordan), and A. surima Schaus. Species in this mimicry complex are generally univoltine, the adults fly- ing during the wet season. They are restricted to forested areas in which the humidity is high all year long. In latitudes south of 23°S, they are found only at elevations above 1000 m. Species in this mimicry complex are characterized by a dark orange and brown striped pattern, and a hindwing upper surface with a dark brown margin from the costal to the anal area, the width ofwhich is di- agnostic for the species. The pattern observed in the under surface of the hindwing, although variable, is one of the most useful diagnostic features for the species. Herein we present descriptions ofthree new cryptic species of Actinote in the "orangish red" complex, commonly misidentified asActinote alalia (Felder). Diagnoses, illustrations ofmale and female genitalia, synonymies, and observations on the natural his- tory ofpreviously described orange-colored species ofActinote also are provided. Currentaddress:DepartmentofBiology,UniversityofOregon,Eugene,Oregon97403,USA 310 Journal ofthe Lepidopterists' Society Materials and Methods The specimens studied are deposited in the following institutions: De- partment ofZoology, Universidade Federal do Parana, Curitiba PR Bra- zil (DZ); Museu Anchieta, Porto Alegre RS Brazil (MAPA). Adults and immatures from two private collections also were studied: Olaf H. H. Mielke (OM, at Universidade Federal do Parana), and R. B. Francini (RBF, now incorporated into the collection ofMuseu de Zoologia USP). Dissections were performed after treatment with 10% KOH. Dissected parts were kept in a solution ofglycerin and 70% ethanol, and are de- posited in the collections along with adult specimens. The presence of pyrrolizidine alkaloids and cyanogenic glycosides was detected using the techniques described in Francini (1989) and Brown and Francini (1990). Actinote dalmeidai Francini, new species (Figs, la, 2a-d, 3a) Actinotealalia D'Almeida 1935a:71,93; Brown 1987:41; Brown 1988:36; Francini 1989:41. Actinote sp. closetoalalia, Brown 1992:158. Diagnosis. Actinote dalmeidai can be distinguished from other species bythe follow- ing features: forewing upper surface orange stripe number 1 and spot number 2 rarely fused. Hindwingundersurfacewhitishyellow, normallywith adarkbrownishorange area present distal to V-shaped mark, variable in size. In males, last tergum ofabdomen short, truncate. Valvae relativelythin andbowed, apex rounded. Ofallorange species presentin Southeastern Brazil, thewingpattern ofA. dahnedai is mostsimilartothatofA. alalia. Description. Male (Fig. la): forewinglength23to34 mm;holotype29 mm. Forewing upper surfacewith orange stripes and spots normallyclearlyseparated bybrown scales, orange stripe number 1 and spot number 2 rarely fused. Hindwing upper surface with same color pattern as forewing, with variable V-shaped mark. Hindwing under surface whitish yellow, somewhat "smoky;" a brownish orange area (darker than upper surface) normallypresent distal toV-shaped mark, more faint towards margin, from nearlyabsent toalmostcoveringentireundersurfaceofthewing,bothdistalandcaudaloftheV-shaped mark; dark margin extended from costal to anal areas visible on under surface. In males, last tergum ofabdomen short, truncate. Male genitalia (Fig. 2a-d): valvae relativelythin andbowed, apex rounded. Shapeoftheuncus+tegumen,juxtaandaedeagusvariable. Fe- male: as describedformale, butupperandundersurfacesofthewingspaler. Femalegen- italia: sterigmasmall, sculptured (Fig. 3a). Distribution. Southeastern Brazilian highlands, known from the states of Rio de Janeiro, Minas Gerais, Sao Paulo, Parana; few specimens known from the states ofSanta Catarinaand Rio Grande do Sul. Types. Holotype male: BRAZIL: Parana, SaoJose dos Pinhais, 850m, 26.XI.1978 (O. H. Mielke) (DZ 3734). Paratypes: BRAZIL: 106 Rio de Janeiro, Maua, Itatiaia 1200m XII.1957 (DZ3126, 3717-21, 3743-44, 3754, 3758); 26 Rio deJaneiro, Resende, Itatiaia, 1200m, 10.1.1973 (DZ3712-13); IdRiodeJaneiroItatiaia, Nordostseite, 1300m,XII.1957 (DZ3722); 26 Rio deJaneiro, Itatiaia, Siidseite, 1100m,4.XII.1963 (DZ3715-16); 16 Rio deJaneiro, Itatiaia, Siidseite, 800m, 12.1.1969 (DZ 3714); 16 Minas Gerais, Juiz de Fora, 500-800m, 17.XI.1953 (DZ 3476); 16 Minas Gerais, Pocos de Caldas, 1250m, 24.12.1966 (DZ3723); 16SaoPaulo, Eug. Lefevre, CamposdoJordao, 1200m,2.XII.1937(DZ3710); 16 Sao Paulo, Eug. Lefevre, Campos do Jordao, 1200m, 17.XII.1952 (DZ 3711); 16 Sao Paulo, Eug. Lefevre, Campos doJordao, 1200m, 8.XII.1957 (DZ3733); 16 SaoPaulo, Bo- racea, Salesopolis, 13.XII.1941 (DZ 3724); 96 Parana, Curitiba, 10.XII.1969 (DZ 3124, 3145,3140,3117,3748-52),26Parana, Curitiba, 13.XII.1968(DZ3753,3756); 16Parana, Curitiba, 20.111.1988 (DZ3742); 16Parana, Piraquara, 13.XII.1969 (DZ3747); 16Parana, Volume 50, Number 4 311 a FlG. 1. Upperand undersurfaces (left and right respectively) ofthreenewspecies of Actinote. (a)A. dalmeidai Francini, newspecies. Holotype6 X¥L3734, forewinglength 29 mm. Seetextforexplanationon stripenumber 1 andspotnumber2; (b)A. catarina Penz, new species. Holotype 6 DZ 3139, forewing length 30 mm; (c) A. bonita Penz, new spe- cies. Holotype6 DZ3761, forewinglength 27 mm. Scalebar: 10mm. 312 Journal of the Lepidopterists' Society Volume 50, Number 4 313 e FIG. 3. FemalegenitaliaofthreenewspeciesofActinote;thelinetotheleftofthefig- ure schematicallyrepresents the cross section. Actinote dahneidai Francini, newspecies. Female genitalia RBF collection: (a) sterigma. Actinote catarina Penz, new species. Fe- malegenitaliaMAPAcollection: (b) sterigma; (c) sphragis.Actinotebonita Penz, newspe- cies. Femalegenitalia DZcollection: (d) sterigma; (e) sphragis. Scalebar: 1 mm. Fig. 2. Male genitaliaofthree newspecies ofActinote. Actinote dahneidai Francini, new species. Male genitalia DZ 3126: (a) dorsal view, (b) lateral view, (c) ventral view; RBF L659#52: (d) 8th sternum. Actinote catarina Penz, new species. Male genitalia MAPA 6011: (e) dorsalview, (f) lateralview, (g) ventralview; DZ 3150: (h) 8th sternum. Actinotebonita Penz,newspecies. MalegenitaliaDZ3118: (i) dorsalview, (j) lateralview, (k)ventralview, (1) 8th sternum. Scalebar: 1 mm. 314 Journal ofthe Lepidopterists' Society Sao Jose dos Pinhais, 850m, 14.XII.1966 (DZ 3746); 16 Parana, Sao Jose dos Pinhais, 850m, 17.XII.1966 (DZ 3745); 13d* Parana, SaoJose dos Pinhais, 850m, 26.XII.1978 (DZ 3141-42, 3149, 3159, 3313, 3730-32, 3735, 3741, 3755, 3757); 15c? Parana, SaoJose dos Pinhais, 850m, 15.XII.1979 (DZ 3114, 3143-44, 3146, 3154-55, 3433, 3475, 3728-29, 3736-40); 16 Parana no date (DZ 3709); 3o Santa Catarina, Sao Bento do Sul, 850m, 2.XII.1969 (DZ3122, 3725, 3727; 16 SantaCatarina, Sao Bento do Sul, 850m, 3.XII.1969 (DZ 3726); 16 Rio Grande do Sul, Cambara do Sul, Itaimbezinho, 2.1.1981 (DZ 3113). Holotype and paratypes at the Department ofZoology, Universidade Federal do Parana, Brazil (DZ). Etymology. The species is named after Romualdo Ferreira D'Almeida (1891-1969). We acknowledge theworkofthispassionate lepidopterist, whotookthe firststeps toward thebetterunderstandingofthetaxonomyofActinote in Brazil. Biology. HOSTPLANTS: Eupatorium punctulatum, Eupatorium sp. (R.B.F pers. obs.). IMMATURES: eggs ofA. dahneidai are barrel-shaped, yellowwhen freshly laid, pale salmonwhen mature; micropyle depression present; deposited in dense clusters of 200-300, packed togethervery closely. Mature larvawith background coloration bluish green; head green; scoli short. Pupawhite with black markings, 5 pairs ofdorsal spines. TOXICITY: pyrrolizidinealkaloidsweredetectedintheadults; strongcyanogenesisispre- sentin all stages (Brown & Francini 1990). MIMICRY: Actinote dahneidai was included inthe"orangishredmimicrycomplex"ofFrancini (1989) and"alalia mimicrycomplex"of Brown and Francini (1990). Actinote catarina Penz, new species (Figs, lb, 2e-h, 3b-c) Diagnosis. Actinotecatarina can be distinguished from other species bythe following features: forewing orange stripe number 1 and spot number 2 frequently fused; other spots also commonly fused. Hindwing under surface colored areagenerallysame orange shade as uppersurface background, distal to theV-shaped mark, variable from absent or pale to large and bright covering more than halfofthe under surface. In males, last ter- gum ofthe abdomen long, pointed. Valvae relativelybroad, apexpointed. As cmpard to the other orange species present in Southeastern Brazil, thewingpattern ofA. catarina canbeconsideredintermediatebetweenthose ofA. conspicua andA. alalia. Description. Male (Fig. lb): forewinglength27to31 mm; holotype30mm. Forewing uppersurfacewith well developed orange stripes and spots, orange stripe number 1 and spot number2 frequently fused; other spots also commonly fused. Hindwing uppersur- facewith same colorpattern as forewing, with variable V-shaped mark. Hindwingunder surfacewhitishyellow;orangecoloredarea(generallysamecolorasuppersurface)located distal to the V-shaped markvaries from absent orpale to large and bright covering more than halfofthe under surface; dark margin extended from costal to anal areas visible on undersurface. Inmales, lasttergum ofabdomenlong,pointed. Malegenitalia (Fig. 2e-h): valvae reasonablybroad, apexpointed. Shape ofuncus+tegumen,juxtaandaedeagusvari- able. Female: asdescribedformale,butupperandundersurfacesofwingspaler; forewing discalcellandanal region moderatelytransparent. Femalegenitalia (Figs. 3b-c): sterigma broad; sphragis broad andhorizontallyattachedtothe abdomen. Distribution. Southern Brazilian highlands, known from the states ofParana, Santa Catarinaand Rio Grande do Sul. Types. Holotype male: BRAZIL: Santa Catarina, Santa Cecilia, 1000m, 22.11.1973 (O. H.Mielke) (DZ3139). Paratypes: BRAZIL: 16"Parana, SaoJose dos Pinhais (DZ3707); Id1 Santa Catarina, Curitibanos, 1050m, 24.11.1973 (DZ 3470); 16 Santa Catarina, Praia Grande Faxinal, 1.1.1984 (MAPA 6828); 16 Santa Catarina, Lages, P.N. Pedras Brancas, 920m, 13.11.1973 (DZ 3706); 16 Santa Catarina, Rio das Antas, 11.1953 (DZ 3705); 26 SantaCatarina, SantaCecilia, 1200m, 22.11.1973 (DZ3150, 3704); 16 Rio Grande do Sul, Aparados da Serra, 1.1985 (MAPA 6829); lc* Rio Grande do Sul, Panambi IV.1973 (DZ 3151); 16 Rio Grandedo Sul, Rio GuaritaXII.1962 (DZ3703); 19 Rio Grandedo Sul, Sao Francisco de Paula, Itaimbezinho 25.1.1959 (MAPA 6615); 19 Rio Grande do Sul, Sao Francisco de Paula 23.1.1959 (MAPA 6612); 29 Rio Grande do Sul, Sao Francisco de Volume 50, Number 4 315 Paula, RS no date (DZ 3702, 3708). Holotype andparatypes at the Department ofZool- ogy, Universidade Federal do Parana, Brazil (DZ), paratypes at Museu Anchieta, Porto Alegre, Brazil (MAPA). Etymology.ThespeciesisnamedafterSantaCatarinastate;A. catarina is restrictedin rangeto southern statesin Brazil. Biology. HOSTPLANTS: unknown. IMMATURES: unknown. TOXICITY: unknown. MIMICRY:Actinotecatarina species fits theattributesofthe"orangish redmimicrycom- plex" ofFrancini (1989) and "alalia mimicrycomplex"ofBrown and Francini (1990), and shouldbe consideredpartofthis complexhereafter. Actinote bonita Penz, new species (Figs, lc, 2i-l, 3d-e) Diagnosis. Actinote bonita can be distinguished from other species by the following features: orangestripes andspotsneverfusedonforewinguppersurface. Hindwingunder surfacewhitish yellow, pale and homogeneous, lacking darkbrown marginal shading. In males, last tergum medium sized. Valvaewide at base, thin from middle portion to apex. Ofallorange speciespresentin Southeastern Brazil, thewingpatternofA. bonita is most similartothatofA. quadra. Description. Male (Fig. lc): forewinglength25to27mm; holotype27mm. Forewing uppersurfacewith orange stripes and spots widely separated bybrown scales. Hindwing uppersurfacewith same colorpattern as forewing, with thinV-shaped mark; dark margin extendedfrom costaltoanalareas slightlydiffuse. Hindwingundersurfacewhitishyellow, pale and homogeneous; darkbrown margin absent, dark-colored scales restricted towing veins. Lasttergum medium sized. Malegenitalia (Fig. 2i-l): valvaewide atbase, thin from middle portion to apex. Aedeagus thin. Shape ofthe uncus+tegumen,juxta and aedeagus variable. Female: as described for male, but upper and under surfaces ofwings paler. Female genitalia (Fig. 3d-e): sterigma longer than broad, mildly sculptured; sphragis delicate. Distribution. Southeastern Brazilianhighlands,knownfromthestatesofMinasGerais and Sao Paulo. Types. Holotype male: BRAZIL: Minas Gerais, Monteverde, Camanducaia, 1650m, 23.XII.1968(DZ3761). Paratypes: BRAZIL: 3c5 Minas Gerais, Monteverde, Camanducaia, 1650m 23.XII.1968 (DZ 3118, 3759-60). Holotype and paratypes at the Universidade FederaldoParana(DZ). Etymology. The species is namedafter"Bonita," asongbyTomJobim. Biology. HOSTPLANTS: Eupatorium inulaefolium (R.B.F pers.obs.). IMMATURES: eggsofActinotebonita arebarrel-shaped,yellowwhenfreshlylaid, faintsalmonwhenma- ture; micropyle depression absent; deposited in clusters of200-400, densityofclusterin- termediate between A. dalmeidai andA. conspicua. Mature larva with background col- oration bluish black; head black; thoracic segments completely black laterally and ventrally; scolishort. Pupawhitewithblackmarkings,5pairsofdorsalspines. TOXICITY: cyanogenesiswas detected in all stages (R.B.F. pers.obs.). Other orange-colored species of Actinote Actinote alalia (Felder) (Fig. 4a-c) Acraea alalia Felder 1860:105; Kirby 1871-77:136; Jones 1883:36; Jones 1883:8; Fritz Miiller 1883:216; Mabille 1896:64. Acraeaeulalia Fritz Miiller 1878:296. Actinotealalia s. alalia Eltringham andJordan 1913:10; Jordan 1913b:374. Actinote alalia Jordan and Eltringham 1916:19; D'Almeida 1935a:93; Ebert 1969:35; Lewis 1975:43, 227; Smart 1976:265; D'Abrera 1987:445; Ackery 1988:136; Francini 1992:16fig.6-14 [ALA]. Acraea (Actinote)alalia Pierre 1987:22. 316 Journal of the Lepidopterists' Society L i L Volume 50, Number 4 317 Diagnosis. Intermediatein size, males 28 to 31 mm (DZ collection). Hindwing under surface greyishyellow; deep orange or, less frequently, brownish orange colored areadis- talto theV-shaped mark, variablein size. Male genitalia (Fig. 4a-c): valvae neitherbroad northin, apexround. Biology. HOSTPLANTS: Eupatorium intermedium and Eupatorium sp. aff. E. inter- medium (R.B.F. pers. obs.). IMMATURES: eggs ofActinotealalia arebarrel-shaped, yel- lowwhen freshlylaid, burgundywhen mature; micropile depression absent; deposited in clusters of200-400, clusterdensitysimilartoA. bonita clusters. Mature larvawith back- groundcolorationpinkishbrown,headblack; scoliveryshort. Pupadarkorangewithblack markings, 5pairsofdorsalspines. TOXICITY: pyrrolizidinealkaloidsweredetectedinthe adults; strongcyanogenesis in all stages (Brown and Francini 1990). MIMICRY: this spe- ciesisincludedinthe "alalia complex"ofBrown and Francini (1990). Actinote conspicua (Jordan) (Fig. 4d-i) Actinotealalia conspicua Jordan 1913a:32; Jordan 1913b:374pi. 82e; Eltringham andJor- dan 1913:10; Jordan and Eltringham 1916:18; Brown and Mielke 1968:151; D'Abrera 1987:445. Actinoteconspicua Ebert 1969:35; Francini 1992:16 fig.6-14 [CON]. Diagnosis. Generally large, males 24 to 38 mm (DZ collection). Orange spots and stripesonuppersurfaceofbothwingsdeepcolored. Hindwingundersurfacedeeporange (but one specimen found (DZ) with the underside ofthe hindwing yellowish colored, maybe still teneralwhen collected). Hindwing darkbrown margin markedlybroad, both on upper and under surfaces. Male genitalia (Fig. 4d-g): valvae long and thin, bowed dorsoventrally.Thisspecieshasthedeepestcolorationamongmembersofitsmimicrycom- plex. Femaleslargerthanmales,onlyslightlypalerthanmales.Femalegenitalia (Fig. 4h-i). Biology. HOSTPLANTS: Mikania hirsutissima (R.B.F. pers.obs.). IMMATURES: presentlyunderstudyby R.B.F. TOXICITY: cyanogenesiswas detectedin eggs and first instarlarvae (R.B.F. pers.obs.). MIMCRY this species was includedin the "orangish red mimicrycomplex"ofFrancini (1989)and"alalia mimicrycomplex"ofBrownandFrancini (1990). Actinote surima Schaus (Fig. 4j-o) Actinote surima Schaus 1902:392; Jordan 1913b:374 pi. 82 f,g; Eltringham and Jordan 1913:13; Jordan and Eltringham 1916:19 Figs. 8, 9; Hayward 1931:29,139pi. 8; Monte 1934:199; Hayward 1935:97; D'Almeida 1935a:94; D'Almeida 1935b:488; Schweizer andWebster-Kay 1941:14; Biezanko and Pitton 1941:9; Hayward 1950:209; Biezanko, Rufinelli and Carbonell 1957:127; Brown and Mielke 1967:151; D'Araujo e Silva et al. 1968:340; Ebert 1969:35; Brown and Benson 1974:218pi. 5 fig.l; Smart 1976:191, 265 pi. 5fig.l; Brown 1984:158; Almeida, Souzaand Marques 1986:33; D'Abrera 1987:445; Francini 1989:44andseveralotherpages,severalfigs; Brown 1988:36; Francini 1992:26 fig.6-14 [SUR]. Fig. 4. Male and female genitalia of orange-colored species ofActinote. Actinote alalia (Felder). Male genitalia DZ 2974: (a) dorsalview, (b) lateral view, (c) ventralview. Actinote conspicua (Jordan). Male genitalia DZ 3130: (d) dorsalview, (e) lateralview, (f) ventralview, (g) 8th sternum. Female genitalia DZ collection: (h) sterigma, (i) sphragis. Actinote surima Schaus. Male genitalia MAPA 6687: (j) dorsal view, (k) lateral view, (1) ventralview; RBF L643#ll: (m) 8thsternum. Femalegenitalia RBF L643F10069#25: (n) sterigma; MAPA 6700: (o) sphragis. Actinotequadra Schaus. MaleOgMenitalia DZ 2970: (p) dorsal view, (q) lateral view, (r) ventral view. Female genitalia 6655, drawn from pinned specimen (s) sterigma. Scalebar: 1 mm. 318 Journal of the Lepidopterists' Society Actinotesurima formapunctata Hayward 1935:97pi. 11 fig. 61; Hayward 1950:209. Acraea (Actinote)surima Pierre 1987:22. Diagnosis. Small, male and female specimens 20 to 30 mm (RBF and MAPA collec- tions). Orange colorslightlylighterthanin otherspecies ofsame mimicrycomplex. Hind- wingunder surfaceyellowish, with same pattern as upper surface; V-shaped mark always welldevelopedinboth upperandundersurfaces. Malegenitalia (Fig. 4j-m): valvaebroad and short, pointedapex. Femalegenitalia (Fig. 4n-o). Biology. HOSTPLANTS: Eupatorium intermedium, Senecio brasiliensis (Francini 1989; Brown & Francini 1990); Mikania hirsutissima, Sijmphiopappus reticulatus (Francini 1989); Eupatoriumbuniifolium (Biezanko et al. 1974); Sijmphiopappus casaret- toi (CM.P. pers.obs.). Biezankoetal. (1974) also listAmaranthus hybridus asahostplant forthis species; becauseActinote larvae fall from the hostwhen disturbed and frequently wanderofftheplant forpupation,we regardthis recordtobe inaccurate. IMMATURES: eggs ofActinotesurima are barrel-shaped, yellowwhen freshly laid, burgundywhen ma- ture; micropyle depression absent; deposited in clusters of200-400, ofdensitysimilarto A. bonita andA. alalia clusters. Mature larvapolymorphic: background colorationvaries from yellowish pink to bluish black, head black; scoli short. Pupawhitewith black mark- ings, 5 pairs of dorsal spines. TOXICITY: pyrrolizidine alkaloids were detected in all stages; strongcyanogenesis was detected in all stages (Brown and Francini 1990). MIM- ICRY: this specieswas includedinthe"orangish redmimicrycomplex"ofFrancini (1989) and "alalia mimicrycomplex" ofBrown and Francini (1990). Actinote quadra Schaus (Fig. 4 p-s) Acraeaquadra Schaus 1902:392; Actinote quadra Jordan 1913b:373; Jordan and Eltringham 1913:13; Jordan and Eltring- ham 1916:18; Lewis 1975:227; Smart 1976:265; D'Abrera 1987:445; Brown 1987:41; Brown 1988:36; Francini 1989:41 and several otherpages; Francini 1992:25 Fig. 6-14 [QUA]. Acraea (Actinote)quadra Pierre 1987:22. Diagnosis. Hindwing under surface whitish yellow, pale and homogeneous, lacking darkbrown marginal shading; dark-coloredscales restrictedtowingveins. Forewingelon- gatedatthetip,withalineofdarkscalesparalleltoitswholebasalarea, resemblingawing vein. Male genitalia (Fig. 4 p-r): with extremelybowedvalvae, unique among southeast- ern BrazilActinote species. Femalegenitalia (Fig. 4 s). Biology. HOSTPLANTS: unknown. IMMATURES: unknown. TOXICITY: unknown. MIMICRY: althoughpreservedspecimensofA. quadra suggestthatthisspeciesisamem- berofthe orangish red mimicrycomplex,whenobservedinflight (R.B.F pers.obs.) itap- pearsthatthis speciesbelongs toadistinct mimicrycomplexthatisthe subjectofafuture study. ACKNOWLEDGMENTS We thank P. R. Ackeryfor kindly doing ablind comparison ofsome ofour specimens with the type material ofActinote alalia deposited at BMNH, and for sending C. M. P slides ofthe type material; R. B. Robbins for sending C. M. P slides ofthe type material depositedat USNM; O. H. Mielkeand M. Casagrande (DZ), M. F. doValand U. R. Mar- tins (MZUSP), and F. R. eyer (MAPA) forprovidingeasy access to the collections under theirresponsibility; A. V. L. de Freitas andA. S. Goncalves forfield assistanceto R. B. F; fKe.llS.owBsrhiopwnt,oCP.. JM..DePVraineds,FAanPdESR.PBf.elSlroywgslheiypftoorRc.oBm.mFe.nmtasdoentthihsesmtaunduyscprosispitb.leA. CNPq LITERATURE CITED ACKERY, P. R. 1988. Hostplants and classification: a reviewofnymphalid butterflies. Biol. Linn. Soc. 33:95-203. J.

See more

The list of books you might like

Most books are stored in the elastic cloud where traffic is expensive. For this reason, we have a limit on daily download.