267,597 research outputs found
Rota-Baxter operators on the polynomial algebras, integration and averaging operators
No full textThe concept of a Rota–Baxter operator is an algebraic abstraction of integration. Following this classical connection, we study the relationship between Rota–Baxter operators and integrals in the case of the polynomial algebra k[x]
k[x]
. We consider two classes of Rota–Baxter operators, monomial ones and injective ones. For the first class, we apply averaging operators to determine monomial Rota–Baxter operators. For the second class, we make use of the double product on Rota–Baxter algebras
MOMJAN IZMEĐU POVIJESTI I KULTURE. DINASTIJA ROTA
No full textIl saggio riassume le vicende del nobile casato dei Rota, originari di Bergamo,
che si insediarono nel castello feudale di Momiano alla metà del XVI secolo
subentrando alle precedenti dinastie dei Duinati e dei Raunicher. Sullo sfondo,
le esigenze di difesa dalle incursioni barbariche e le lotte di potere fra Patriarcato
di Aquileia, Contea di Gorizia e Repubblica di Venezia. Quest’ultima lasciò
un’impronta indelebile nella cultura, nel paesaggio urbano e nel contesto sociale
di questa parte dell’Istria.Na temelju različitih povijesnih izvora i dokumenata sačuvanih u javnim i
privatnim arhivima, članak rezimira epopeju feudalne zajednice koja je živjela
na području Momjana u sjeni poznatog dvorca, osnovanog oko 1000. godine,
a zatim ojačanog i obnovljenog u više navrata od strane Devinskih grofova,
Raunichera i konačno dinastije Rota koja je njime upravljala gotovo tri stoljeća,
počevši od 1548. U pozadini, tekst otkriva potrebe za osiguranjem egzistencije
i obranom stanovništva od barbarskih prepada i upada, kao i borbe za
prevlast između Akvilejskog patrijarhata i Goričkih grofova koji su se pokušali
suprotstaviti dominaciji Mletačke republike. Ova potonja je ostavila neizbrisiv
trag u kulturi i civilizaciji u urbanom i društvenom krajoliku ovog dijela Istre i
šire, koji je trajao i nakon kraja feudalizma i pada Serenissime 1797. godine. U
tom je razdoblju, međutim, započela prijelazna faza u kojoj su drevne potrebe
za zaštitom iza zidina zamijenjene novim prioritetima ekonomske prirode i
modernizacijom životnih uvjeta. Sljedeće generacije ove loze, osim što su
zadržale značajnu prisutnost u Momjanu, razgranale su se u brojnim obiteljskim
ograncima u piranskom, vodnjanskom, tršćanskom području i u Julijskoj krajini,
s poznatim ličnostima u humanističkim znanostima i glazbi
Halma Angélico y la revista Mujer (1931)
No full textIl contributo esamina la collaborazione di Halma Angélico con la rivista "Mujer", pubblicata a Madrid dal giugno al dicembre del 1931. Ci si sofferma in particolare su quegli articoli che trattano i temi più sensibili dell'epoca: la partecipazione femminile alla vita politica, l'associazionismo, il diritto di voto, la condizione femminile e la patria potestà
Achaeta etrusca Rota 1995
No full textAchaeta etrusca Rota, 1995 (Figure 4) Achaeta etrusca Rota, 1995, pp. 197–198, figure 8A–C. Achaeta etrusca, Rota et al. 2013, table 1 and figure 3 (species ‘s5’); Rota et al. 2014, tables 1, 2 and Suppl. 1. Material examined Type material. MCZR Oligochaeta 0049–0050, Holotype and one paratype from Italy, Tuscany (Tu-3), Rovine di Castelvecchio (43.4320°N, 11.0052°E, 400 m asl), about 4 km Ν of Castel S. Gimignano, 8 km SW of San Gimignano (Siena). Oak wood on limestone, pH 7.1–7.3, 23.05.1994, E. Rota coll. New material (in the author’ s collection). About 150 specimens from Italy, Campania (Ca-2), plots N1 – N3, 13.05.2009 and 26.10.2009. Nine specimens from Italy, Tuscany (Tu-4), 8– 16.06.2004. Seven specimens from Italy, Tuscany (Tu-5), 24.04.2009 and 05.11.2009. Augmented diagnosis Live body length 2.0– 3.5 mm, width 0.15–0.21 mm at XII. Segments 21–24. Paired knob-like cutaneous gland structures dorsolateral in II– VI (Figure 4A). Clitellum laterodorsally made of hyaline cells irregularly scattered among granular cells, with a narrow middorsal interruption (25 μm); ventrolaterally only granular cells occur; clitellum absent midventrally (gap as wide as the distance between male pores, 64 μm). Secondary pharyngeal glands in V and VI. Pronounced oesophageal loops in IV and VII, visible both in vivo (Figure 4B, C) and in fixed material. Dorsal blood vessel originating in VII and entering directly into VI, i.e. bypassing the oesophageal loop of VII. Three pairs of preclitellar nephridia (6/7–8/9). Sperm funnels 48–53 by 27–35 μm. Sperm heads about 15 μm long, tails 25 μm. Penial bulbs in XII, compact, oval, 32 μm long. One egg mature. Remarks The validity of this species has recently been questioned by Graefe (2007), and its synonymization with A. iberica has been proposed (Schmelz and Collado 2010, 2012). The original description (Rota 1995) mentioned ‘inconspicuous lens-shaped epithelial cells observed dorsolaterally from II’. These words have been misinterpreted as if referring to the lentiform gland cells segmentally punctuating the sides of the body of A. iberica at three distinct levels, but the structures of A. etrusca swell inwards, occur as one dorsolateral pair per segment and are limited to segments II–VI (in segment I, more dorsal and bilobed structures occur, probably of a different nature) (Figure 4A). Thus they would rather seem homologous to the ‘dorsolateral epidermal follicles slightly protruding into the body cavity’ characterizing segments I, III–VI in A. antefolliculata Dózsa-Farkas and Boros, 2005. Differences between A. etrusca and the latter include the number of secondary pharyngeal glands (two vs. one pair) and the pairs of preclitellar nephridia (three vs. two). Distribution This species was discovered originally in oak woodland soil on limestone in central Tuscany. The present new records in the outskirts of Siena and in Capodimonte Park, Naples city, confirm its association to evergreen Mediterranean woodland and scrubland on neutral soils. In Capodimonte Park it appeared equally abundant in spring and autumn.Published as part of Rota, Emilia, 2015, Five new species of Enchytraeidae (Annelida: Clitellata) from Mediterranean woodlands of Italy and reaffirmed validity of Achaeta etrusca, Fridericia bulbosa and F. miraflores, pp. 1987-2020 in Journal of Natural History 49 (33) on pages 1999-2001, DOI: 10.1080/00222933.2015.1009514, http://zenodo.org/record/399798
Nino Rota al servizio di Visconti : il caso di «Rocco e i suoi fratelli»
No full textL'intervento ricostruisce forme ed esito della collaborazione tra il compositore Nino Rota e il regista Luchino Visconti in occasione del film "Rocco e i suoi fratelli" (1960)
Il Rota, overo, Delle imprese dialogo /
No full textSignatures: *² a-h⁸ I⁴.Errata: p. [6] at end.Giunti device on t.p. Two historiated initials, one floriated."Gli interlocutori sono m. Nino di Nini vescouo di Potenza, il s. Berardino Rota, il s. Alfonso Cambi, & m. Bartolomeo Maranta"--P. 3.First published Naples : Gio. Maria Scotto, 1562; see Praz.Praz, M. 17th-century imagery (2nd ed.),Mode of access: Internet.Bound with: Dell'imprese scelte / Simon Biralli. Venice : G.B. Ciotti, 1600 (SPECIAL 85-B26599).Library's copy lacks leaf a1 with p. 1-2
Luchino Visconti: Senso, musica di Nino Rota
No full textNei titoli di testa di Senso il nome di Nino Rota non compare. Troviamo, invece: «Commento musicale: Anton Bruckner, Sinfonia n.7 in Mi maggiore. Orchestra Sinfonica della Radiotelevisione italiana diretta da Franco Ferrara". Dimenticano, i titoli di testa, che la colonna sonora del film, sebbene non contenga una sola nota del musicista, possiede alcune preziosità che non dovrebbero far passare in secondo piano la mano di chi ha organizzato e montato quella partitura cinematografica, rendendola ideale commento sonoro per questo atipico racconto filmico. L'articola analizza dettagliatamente la partitura del film, organizzata com'è noto nel sapiente montaggio dei temi dei primi due movimenti della "Settima Sinfonia" di Anton Bruckner e di alcuni luoghi del "Trovatore" verdiano, mettendo in mostra il prezioso lavoro di Nino Rota
"Musica clandestina": i concerti per ottone di Nino Rota
No full textI concerti per ottone e orchestra di Nino Rota (Concerto per trombone e orchestra, 1966; Ballata “Castel del Monte” per corno e orchestra, 1974) rientrano perfettamente nella definizione che Fedele d'Amico diede della musica di Rota: musica clandestina. Sono rivolti a quella parte di pubblico che non aderisce alle istanze ideologiche-musicali del secondo Novecento (un uditorio clandestino), e sono composti in uno stile accessibile e per nulla rivoluzionario (ossia pienamente neoclassico). Ciononostante nella loro scrittura appare chiaro uno stretto collegamento fra l'idea compositiva di Rota e due concetti fondamentali della sua contemporaneità. L'esplorazione del timbro e delle capacità tecniche di uno strumento tanto antico quanto poco sfruttato in ambito solistico, è l'ambito in cui si muove il Concerto per trombone; il rapporto intermediale fra narrazione, immagine e musica, oltre che con una delle grandi passioni di Rota, l'esoterismo, è invece il fulcro della Ballata per corno “Castel del Monte”
Fridericia bargaglii Rota 2015, sp.nov.
No full textFridericia bargaglii sp.nov. (Figures 5–6) Fridericia polychaeta, Rota 1995, p. 215 (partim) Fridericia sp. 3, Rota et al. 2013, tables 1 and figure 3 (species ‘s27’); Rota et al. 2014, tables 1, 2 and Suppl. 1. Type material Holotype. MCZR Oligochaeta 0179, whole-mounted specimen, fully mature. Type locality Italy, Tuscany ( Tu-6 ), Siena city, Orti dei Tolomei (43.3146°N, 11.3324°E, 330 m asl), grass under Laurus nobilis shrubs on yellowish-brown sandy soil, 31.03.2004, E. Rota coll. Paratypes. MCZR Oligochaeta 0180, one whole-mounted submature specimen, from Italy, Tuscany (Tu-8), 01.04.1992. MCZR Oligochaeta 0181, one wholemounted specimen, submature, from Italy, Tuscany (Tu-5), 04.11.1993. SMNH- Types 8723–8724, two whole-mounted specimens, submature, from type locality and date. Other material. Several specimens, whole mounted or fluid preserved, from Italy, Tuscany, loc. Tu-3, Tu-5, Tu-6, Tu-7, Tu-8, Tu-9, Tu-10, in the author’ s collection. Etymology Named for Prof. Roberto Bargagli, for his dedication and achievements in environmental research, and with thankfulness for his enduring friendship and support. Diagnosis Large multisetose species (4÷7 – 6÷2: 4÷7 – 6÷2), clitellar gland cells in indefinite rows, ventrally reduced to a narrow strip behind male pores, extra lobes of pharyngeal glands ventrally in VII, nucleated coelomocytes large and pale, peptonephridia multi-branched at two distinct levels, five pairs of preclitellar nephridia, chylus cells in XIII–XV, dorsal blood vessel from XVIII–XX, large seminal vesicle, sperm funnels elongate conical, male slits I-shaped (longitudinal), subneural glands in XIII–XV, spermathecae large, elongate, with two toe-shaped aciliated diverticula and no distinct ectal gland. Description Colour white-yellowish, paler after storage in alcohol. Live body length 17–28 mm, width about 0.67–0.83 mm at XII; dimensions can be large also in fixed specimens: length 25 mm, width 0.55–0.60 mm at V, 0.8 mm at XII. Segment number 56–73, x = 63.5, s = 6.2 (n = 31). Prostomium 1.2 times longer than peristomium, frontally rounded, blunt conical in a lateral view, dorsally depressed in front of head pore, pointing forwards (Figure 5A). Epidermal sensory buds abundant on prostomium, segments I–II and pygidium. Epidermal glands small, dot-shaped, arranged in four complete transverse rows per trunk segment. Clitellum (Figure 5B) slightly elevated (30 μm), interrupted ventrally except immediately behind male openings in XII where a strip of both hyaline and granular cells occurs; both types of gland cells small, 12–18 by 8–12 μm, arranged in indefinite rows, the granular type twice as numerous as the hyaline type. Subneural glands on nerve cord midventral in IV (Figure 5B) and in XIII–XV, located either at the segment equator, or between the ventral chaetal bundles, or in the intersegment. Sometimes also a papilla midventral at 12/13. Head pore at 0/1, oval (50 μm long). Dorsal pores from VII. Spermathecal pores in ‘lateral lines’ at 4/5, surrounded by glandular epidermis. Male pores as I-shaped longitudinal slits, with distinct, asymmetrical, transverse extensions. Chaetae weakly hooked entally, 4÷7 – 6÷2: 4÷7 – 6÷2, but specimens with maximally six chaetae in preclitellar bundles are very frequent. Caudal bundles reducing to two or three chaetae only in last 10 segments. In fixed specimens, ectal tips of chaetae pointing posteriorly in anterior 25 segments, thereafter showing the opposite orientation. Length of chaetae maximal caudally, reaching 120–150 μm. Cuticle thin, less than 2 μm thick throughout. Body wall thick but soft and relatively transparent. No thickened septa. Brain (Figure 5A) oval, with shallow anterior convexity, in vivo 190–204 by 135–146 μm. Peptonephridia ending in VI or VII, each consisting of a stout stem giving off many thin, long, equal-sized, straight branches at two distinct levels, proximally (or at midlength) and terminally (type c sensu Nielsen and Christensen, 1959) (Figure 6D). Pharyngeal glands four pairs, three of which partly merging dorsally at 4/5–6/7, plus extra lobes ventral in VII (Figure 6A). Five pairs of preclitellar nephridia (6/7–10/11), with efferent ducts arising antero- to midventrally from postseptal. Coelomocytes: nucleated cells in vivo opaque when accumulated, filled with fine pale granules, up to 50–60 μm long, with very small nucleus; anucleate corpuscles small, 5–10 μm long. The worms discharge abundant coelomic fluid that coagulates at fixation. Chloragogen cells from V. Chylus cells in XIII–XV or XIII–1/2XVI. Ventral intestinal ridge not clearly visible. Dorsal vessel most frequently originating in XVIII–XX, with four pairs of thin lateral commissures: two starting from a common root in III, one in IV and one in V. Seminal vesicle occupying 2–3 segments within X–XIII (Figure 5C), forming paired bulgings at both ends. Sperm funnels (Figure 5C) elongate conical, tapering toward vas deferens, each 600–900 μm long and 180–250 μm broad in its proximal one-third (which in vivo appears opaque). Collar distinctly set off, 7 μm high, slightly narrower or as wide as funnel. Heads of spermatozoa about 130 μm long. Vasa deferentia 11 μm thick in vivo. Each penial bulb 150–170 μm long (fixed). Up to two eggs mature. Spermathecae (Figure 6A–C) independently communicating with the dorsal side of gut entally at 5/6; ampulla elongate with two stalked diverticula (resembling big toes) apically converging toward the ectal duct. Total width of ampulla and diverticula 204–235 μm. Each diverticulum 83–105 μm wide, ending with a large hemispherical (toe-nail shaped) sperm chamber (Figure 6B, C). Inner wall of ampulla pimpled throughout. Inner wall of diverticula not ciliated. Sperm mass not rotating inside the diverticula. Ectal duct 500–550 μm long (1.5–2 times the ampulla) and only 25–30 μm thick in vivo; duct canal straight, of uniform width (2.5 μm); duct projecting into ampulla as a broad bulb lined by tall cells. Some small, indistinct gland cells at spermathecal ectal pores. Remarks This species has been earlier (Rota 1995) confounded under the name of F. polychaeta Bretscher augm. Southern (1907). After the improved characterization and recognition of the latter taxon as a new distinct species, F. healyae, by Schmelz (2003), and following personal observations on Swedish material of F. healyae (see Erséus et al. 2005), I was able to separate the Italian material compiled in Rota (1995) into specimens belonging to F. healyae (sample from site Tuscany 17) and specimens belonging to the present new species (all remaining Tuscan samples). In F. healyae the clitellum is girdle-shaped and the gland cells are arranged to form an irregular honeycomb tiling, with a ratio between hyaline and granular cells of 1:4 (pers. obs.). In F. bargaglii sp. nov. the two types of cells occur with a ratio of about 1:2 and the clitellum is nearly absent ventrally. Other important differences from F. healyae are the two-level branching of peptonephridia, the always welldeveloped seminal vesicle, the extra pair of pharyngeal glands in VII, the many subneural glands and the absence of inner ciliation in the spermathecal diverticula. F. bargaglii sp. nov. differs from F. polychaeta Bretscher, 1900 as originally defined (whether or not one accepts the latter as a valid taxon), by its brain shape, the number of pharyngeal glands, the origin of the dorsal vessel, and the habitat (unlike F. bargaglii sp. nov., both F. healyae and F. polychaeta appear to be associated with wet soils). Distribution Apparently endemic to Tuscany, associated with neutral soils. Recent studies (Rota et al. 2013, 2014) have confirmed the abundance of this species in urban (Villa Patrizia, plots S2 and S3) and suburban (Belcaro) districts in Siena.Published as part of Rota, Emilia, 2015, Five new species of Enchytraeidae (Annelida: Clitellata) from Mediterranean woodlands of Italy and reaffirmed validity of Achaeta etrusca, Fridericia bulbosa and F. miraflores, pp. 1987-2020 in Journal of Natural History 49 (33) on pages 2001-2005, DOI: 10.1080/00222933.2015.1009514, http://zenodo.org/record/399798
Alasea corniculata Rota, new species
No full text<i>Alasea corniculata</i> Rota, new species <p>Figs. 1–8</p> <p> <b>Description. Male.</b> <i>Head:</i> Frons and vertex dark fuscous with metallic blue-green sheen. Eye bordered by orange-yellow scales mesally, ventrally, and laterally (Fig. 2). Labial palpus orange-yellow laterally and pale yellow mesally, with dark fuscous tip (in some specimens reduced to a few fuscous scales) (Fig. 2). Proboscis with pale yellow scales basally. Antenna fuscous with metallic purple sheen, flagellomeres from about 0.3 to 0.7 length of antenna with patches of silvery-white scales (Fig. 4).</p> <p> <i>Thorax:</i> Dark fuscous with metallic blue-green sheen; ventrally with large creamy-yellow scales anteriorly; creamy-yellow band from head towards wing base (Fig. 3). Legs with alternating fuscous and orangeyellow bands on tibia; tarsus with alternating fuscous and white bands; each of these light-colored bands on tibia and tarsus accompanied by elongate piliform scales of same color (Fig. 3). Forewing length 4.5–5.2 mm (n = 10). Upper side dark fuscous with irregular silvery-white streaks and spots (Fig. 1). Incomplete antemedial band formed by silvery-white scales. Silvery-white streak at 0.6 costa curving towards apex. Underside fuscous with metallic bronze sheen; longitudinal orange-yellow streak from base towards apex to 0.75 length; orange-yellow spot above this streak approximate to wing center. Fringe light fuscous, with some pale-tipped scales, and with metallic sheen. Hindwing with upper side orange-yellow; with area of dark fuscous scales at base, apex, and anal region; area of white scales along costal margin (Fig. 1). Black terminal band from costa, starting before apex and extending to the anal area. Fringe light fuscous with metallic sheen; most scales paletipped. Underside similar to upper side, but dark fuscous scales absent at base and apex, present only in anal region, sometimes in streaks, sometimes covering entire anal area.</p> <p> <i>Abdomen:</i> Light fuscous with seven irregular orange-yellow annulations posteriorly on each segment; annulations more pronounced dorsally than ventrally. Genitalia (n = 8) as described for genus (Figs. 6, 7).</p> <p> <b>Female.</b> <i>Head and thorax:</i> As described for male. Length of forewing 5.2–5.7 mm (n = 9).</p> <p> <i>Abdomen:</i> Genitalia (n = 5) as described for genus (Fig. 8).</p> <p> <b>Holotype.</b> Male, Costa Rica, Province Heredia, La Selva Biological Station, 50–150 m, 10º26’ N, 84º01’ W, 22–29 Jan 2000, at MV light, L/00/666, coll. D. Wagner, CRI 002724390, genitalia slide JR 2008-50. Holotype deposited in INBio.</p> <p> <b>Paratypes.</b> Costa Rica: Province Heredia: La Selva Biological Station, 50–150 m, 10º26’ N, 84º01’ W, 8– 25 Mar 1999 (1 ɗ), area laboratorios, L/00/594, CRI 002739331, genitalia slide JR 2008-48 (JR collection); 22–31 Mar 2001 (2 ɗ), at MV/UV light, colls. D. Wagner, J. Rota, INB0003205582, genitalia slide JR 2008- 49 (USNM) and INB0003205569, genitalia slide JR 2008-47 (BMNH); 20 Apr 1999, bosque secundario, L/ 08/621, CRI 001284938 (1 ɗ) (RMNH) and CRI 001284937 (1 &), wing slides JR2003-1 and JR2003-2 (INBio); 23–29 Feb 2004 (1 &), at MV light, coll. D. Wagner, INB0003609767, genitalia slide JR 2008-51 (USNM); 9 Mar 2004 (1 &), canopy UV light trap, colls. G. Brehm, J. Rota, INB0003611787, genitalia slide JR 2008-52 (JR collection); 10–25 Jan 1999 (1 ɗ), at light, coll. D. Wagner, genitalia slide JR 2008-45 (UCMS); 28 Jun 1994 (1 &), bosque secundario, L/06/107, CRI 001243945 (INBio); 10 May 1996 (1 &), biblioteca, L/04/237, CRI 002062296, genitalia slide JR 2008-29 (INBio); 6 Apr 1999 (1 &), bosque primario, L/ 09/610, CRI 001285629 (INBio). Braulio Carrillo NP, Est. Magassay, 200 m, Dec 1990 (1 ɗ), L N 264600 531100, coll. M. Zumbado, CRI 000228433, genitalia slide JR 2008-46 (INBio); 11 km ESE La Virgen, 250– 350 m, 10º21’ N, 84º03’ W, 17 Mar 2004 (1 &), 03/L/00/034, UV light trap, coll. J. Rota, INB0003611759, genitalia slide JR 2008-24 (INBio). Province Puntarenas: Osa Peninsula, 200 m, bosque esquinas, Mar 1994 (1 ɗ), coll. M. Segura, L S 301400_542200, #2776, CRI 001757112, genitalia slide JR 2008-26 (INBio); Corcovado NP, Sirena, 15–16 Aug 1980 (1 &), colls. D. H. Janzen and W. Hallwachs, INB0003868490, genitalia slide JR 2008-25 (INBio). Province Limon: Sector Cerro Cocori, Finca de E. Rojas, L N 286000 567500, coll. E. Rojas, 150 m, Jan 1992 (1 ɗ), CRI 000332924, genitalia slide JR 2008-23 (INBio); Nov 1990 (1 &), CRI 000594414, genitalia slide JR 2008-29 (INBio); Mar 1992 (1 ɗ), CRI 000363517, genitalia slide JR 2007- 28 (INBio).</p> <p> <b>Remarks.</b> This species is relatively uncommon; it is encountered at lights and in light traps in primary and secondary forest.</p> <p> <b>Etymology.</b> The species is named for the horn-shaped projection on the valva. The word is derived from the Latin adjective <i>corniculatus</i>.</p> <p> <b>Discussion.</b> Currently, <i>Alasea</i> is known only from a few localities in Costa Rica. Its biology and immature stages are unknown. <i>Alasea</i> can be assigned to Choreutinae with little question. As with other choreutines, its forewing and hindwing have an acute, bluntly pointed apex (not obtuse as in Brenthiinae) (see Arita 1987, Diakonoff 1986); the basal segment of the labial palpus is parallel-sided (not narrowed basally as in Brenthiinae) (see Arita 1987); the hindwing is orange-yellow (as in many species of <i>Choreutis</i>, <i>Hemerophila</i>, and <i>Rhobonda</i>, but not in Brenthiinae); the basal flagellomeres of the antenna are heavily scaled (no such scaling occurs in Brenthiinae). In addition, preliminary results of an analysis of molecular data (to be published elsewhere) place it convincingly within Choreutinae. <i>Alasea</i> shares the presence of a small spine at the apex of the valva with <i>Hemerophila</i>, <i>Rhobonda</i>, and <i>Zodia</i>. This spine is variably developed in these groups, and it is unclear whether it represents a synapomorphy.</p>Published as part of <i>Rota, Jadranka, 2008, A new genus and new species of metalmark moths (Lepidoptera: Choreutidae) from Costa Rica, pp. 12-18 in Zootaxa 1933</i> on pages 15-17, DOI: <a href="http://zenodo.org/record/274598">10.5281/zenodo.274598</a>
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