Triphosa sabaudiata ( Duponchel, 1830 )
publication ID |
https://doi.org/ 10.11646/zootaxa.4603.1.2 |
publication LSID |
lsid:zoobank.org:pub:01119552-8BF7-4FCA-9BAE-0E8795FA41CD |
persistent identifier |
https://treatment.plazi.org/id/092587AB-E865-FF85-FF44-FC50FBB5F9D5 |
treatment provided by |
Plazi |
scientific name |
Triphosa sabaudiata ( Duponchel, 1830 ) |
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Triphosa sabaudiata ( Duponchel, 1830) View in CoL
( figs 16 View FIGURES 13–17 , 27–30 View FIGURES 20–37 , 41, 42 View FIGURES 41–43 , 49 View FIGURES 46–49 ; map)
Larentia sabaudiata Duponchel, 1830 View in CoL . In: Godart, J.B. & Duponchel, P.A.J., Histoire naturelle des lépidoptères ou papillons de France, 8 (1), 370. Syntypes (France, Aix en Savoie).
Larentia millierata Bruand, 1855 View in CoL . Annales de la Société entomologique de France, 3 (1), LIX. Holotype (France, Mont d’Or, near Ferrière).
Triphosa agnata Le Cerf, 1918 View in CoL . Bulletin du Muséum national d'histoire naturelle. Paris 1918 (6), 412. Holotype ♂ ([Turkey]: ‘ Césarée ( Cappadoce )’). Deposited in France, Paris, Muséum National d’Histoire Naturelle. Hereby regarded as a new synonym of Triphosa sabaudiata View in CoL (see remark).
Type material examined. ( Holotype of T. agnata syn. n., figs 27 View FIGURES 20–37 , 42 View FIGURES 41–43 ) 1 ♂, Cesarée, Type, F. LeCerf det. 1918, gen. prep. 223; in MNHM .
Further material examined. 1 ♂, [ Turkey] Isparta (in cave), Yalvac-Turkey , 19.x.2016, leg. Gökhan Aydin ; 1 ♀, Borabey-Amasya , Turkey, 14.vi. 2003, 1066 m, N 40°48’12’’ E 36°08’52’’, leg. Feza Can; all in MKU GoogleMaps . 1 ♀, Gümüschrhane , ex coll. Staudinger, g. prep 0021/2018 D. Wanke ; 2 ♀, Amasia, ex coll. Staudinger, g. preps 0022, 0023/2018 D. Wanke; all in MNHU . 1 ♀, Türkei, Prov. Antalya, 17.iv.2001, ca. 1200 m, Civizli W Seydisehir, leg. Bernd Schacht, BC Lep DS 0011, g. prep 0032/2018 D. Wanke; in PCDS . 1 ♀, Montenegro / Crna Gora mer. Lovcen NP. E-Seite, Jezerski vrh, Njegos Mausoleum und Umgebung , ca. 1550–1657 m, 25.vii.2009, leg. L. Lehmann, BMB Lep 00790, g. prep 0038/2018 D. Wanke; in PCJG . 1 ♀, S-Türkei, Taurus: Camliyayla bei Tarsus , 1300–1400 m, 10.–14.vi.1996, leg. J. Gelbrecht, S. Beshkov & T. Drechsel, BMB Lep 00792, g. prep 0036/2018 D. Wanke . 1 ♂, Türkei, Pontisches Gebirge, Ilgaz Daglari Ilgaz , ca. 800 m, 6.vii.1990 LF, leg. J. Gelbrecht & E. Schwabe, BMB Lep 00791, g. prep 0037/2018 D. Wanke; all in PCJG . 1 ♀, Erciyes Dagi, Kayakeri , prov. Kayseri, Turquie, 2100 m, 10.vii.1990, leg. E. Drovet, g. prep 0055/2018 D. Wanke ; 1 ♀, Turkey, Prov. Kayseri, 5 km. nw. Ercios Dagh , 2000 m, 22.vii.1986, leg. M. Fibiger, g. prep 0056/2018 D. Wanke; all in PCPS . 1 ♀, Tirol , e.l. 21.vi. [19]40, Fleiss Innsbruck, g. prep 752/2009 H. Rajaei ; 1 ♂, 1 ♀, Turkey, Prov. Kayseri, 5km. nw. Ercios Dagh. , 2000 m, 22.vii.1986, leg. M. Fibiger, ex coll. Michael Fibiger, SMNK; E. Lep 281, g. prep (♂) 0143/2018 D. Wanke ; 8 ♂, 6 ♀, Turkey, Prov. Kayseri, 20 km S, 2000 m, Erciyas Dagi , 28.vii.1989, leg. Fibiger & Esser, ex coll. Michael Fibiger, SMNK; E. Lep 281, g. prep (♂) 0144/2018 D. Wanke; all in SMNK . 2 ♂, 1 ♀, Gempenhöhle , 29.xii. [19]47, g. prep (♂) 1911/2015 H. Rajaei ; 2 ♂, 1 ♀, Gempenhöhle , 23.xi. [19]47, g. prep (♂) 0024/2018 D. Wanke ; 1 ♂, Gempenhöhle, 30.xii.1956, coll. W. Schäfer, Stuttgart, SMNS-Lep.1997-11 ; 1 ♀, Gempen , 7.i. [19]50, coll. W. Schäfer, Stuttgart, SMNS-Lep.1997-11 ; 1 ♀, Gempen , 25.vii. [19]55, coll. W. Schäfer, Stuttgart, SMNS-Lep.1997-11, g. prep 0005/2018 D. Wanke ; 2 ♂, 2 ♀, Bas. Jura, Gempenhöhlen , 8.ix. [19]46, Wolf ; 1 ♂, Gempen, i.[19]59, B. Blattner, g. prep 0052/2018 D. Wanke ; 1 ♀, Croatia, di Frasassi, Ancona, ix.1956, coll. W. Schäfer, Stuttgart, SMNS-Lep.1997-11 ; 1 ♂, Schwäb. Alb, 1894, Fauna Baden-Württemberg , Funddaten registriert 1995/1996 ; 2 ♂, Rosenstein , Heubach , 5.xi. [19]06, Fauna Baden-Württemberg , Funddaten registriert 1995/1996 ; 1 ♂, Herrlingen b. Ulm , Tiefental, G. Hammer, Fauna Baden-Württemberg , Funddaten registriert 1995/ 1996 ; 1 ♂, Reiteralm Höhle , 1650, 1.xi. [19]65, Dr. Stüber , leg. K. Mazzucco, Salzb .; 1 ♂, Ob. Öst. , Schönbg. Alm , 10.viii. [19]53, R. Löberbauer ; 1 ♂, Oberdonau , Traunstein , 500 m, 24.xi.1949, Foltin ; 1 ♂, Preda, ex Coll. W. Pfitzenmeier Stuttgart, g. prep 0001/2018 D. Wanke; (more specimens from France, Italy and Switzerland examined), all in SMNS . 1 ♂, Asia min., Turcia, Kizilcahamam , 952 m, 23. u. 24.vi.1969, leg. G. Friedel, g. prep 0149/2018 D. Wanke ; 1 ♂, Asia min., Ankara-Barrage , 13.–17.vi. [19]66, leg. Friedel, g. prep 0151/2018 D. Wanke ; 1 ♂, Asia minor, Barrage , 10 km no Ankara, 1100 m, 13.–17.vi. [19]66, R. Löberbauer, g. prep 0152/2018 D. Wanke; all in ZSM .
Remark. Triphosa sabaudiata and T. agnata syn. n. share the genitalia characters, which are most diagnostic in this species-group (e.g. socii weakly developed on protrusions at the uncus base; labides fused into one long and thin stick) ( figs 41, 42 View FIGURES 41–43 ).
Diagnosis. Wingspan 38–45 mm, rarely 32–38 mm (length of forewing 20–25 mm), no sexual dimorphism in size. Ground colour from pale grey to bright yellowish-white, with some grey shine (greyish brown, with red shimmer in T. dubitata ; beige, sandy coloured in T. silviae sp. n.; beige, from sand-coloured to very bright brown in T. lecerfi sp. n.; sandy-yellow covered with a slate-coloured shroud in T. taochata ). Transversal lines faint, sometimes slightly visible. Wing pattern stronger towards costa. Colour of fringes not differing from the ground colour ( figs 27–30 View FIGURES 20–37 ).
Male genitalia ( figs 16 View FIGURES 13–17 , 41, 42 View FIGURES 41–43 ). Uncus base with protrusions carrying weakly developed socii on each side (few setae at the base of the uncus in T. dubitata and T. silviae sp. n.; more setae at the uncus base in T. lecerfi sp. n.; setae located on protrusions in T. taochata ) ( figs 13 View FIGURES 13–17 a–17a). Labides fused into one long and thin stick reaching further than the uncus base; labides tip covered with setae (hump-shaped, not touching each other, equipped with setae in T. dubitata ; flat, thickened to the centre and setose in T. silviae sp. n.; thin, flat, strongly and densely setose in T. lecerfi sp. n.; spoon-shaped, fused, tip strongly setose in T. taochata ) ( figs 13 View FIGURES 13–17 b-17b). Juxta three-lobed. Sacculus projection distally forked, heavily sclerotized; fork-shaped tip consists of two identical prongs, the angle between the prongs being ~45° (lower prong shorter than upper one, upper prong curved, both arranged in less than 90° in T. dubitata ; prongs slightly different with upper prong longer and broader, both arranged in less than 90° in T. silviae sp. n.; both prongs blunt and short, arranged in more than 90° in T. lecerfi sp. n.; upper prong long, lower prong shortened, arranged in ~90° in T. taochata ) ( figs 13 View FIGURES 13–17 c–17c).
Female genitalia ( fig. 49 View FIGURES 46–49 ). Ovipositor broad, antrum short, wide and funnel-shaped. Ductus bursae bent, very short, flat, wide in ventral view, but narrow in lateral view. Corpus bursae pyriform, its posterior part funnelshaped, heavily sclerotized with longitudinal folds; its anterior part bag-shaped; membranous (similar in T. silviae sp. n., T. lecerfi sp. n. and T. taochata ; ‘guitar-shaped’, posterior part of corpus bursae tubular, heavily sclerotized with few longitudinal folds; anterior part membranous, in T. dubitata ) ( figs 46–52 View FIGURES 46–49 View FIGURES 50–53 ).
Phenology. Univoltine. One very long generation of about nine months (emerging late June or early July; both sexes hibernating in caves; in spring active from April to late May) ( Ebert 2001; Hausmann & Viidalepp 2012).
Biology. Larva monophagous on Rhamnaceae ( Rhamnus pumilus , R. saxatilis , R. cathartica ), observed nectarfeeding of adults on Clematis vitalba and Adenostyles ( Heinicke & Müller 1976; Ebert 2001; Hausmann & Viidalepp 2012).
Habitat. Mountain regions, troglophilous ( Hausmann & Viidalepp 2012). Flying in rocky slopes, lime rocks, rocky valleys and often found when resting in dry caves ( Heinicke & Müller 1976; Hausmann & Viidalepp 2012). Occurring at altitudes from 600–2700 m ( Ebert 2001; Hausmann & Viidalepp 2012).
Distribution. West-Palaearctic, with fragmented distribution from western Europe to the Balkan Peninsula and Turkey. Outside Europe, its range extends from northern Morocco to the central Asian mountains ( Hausmann & Viidalepp 2012). Distribution in the Middle East and Central Asia reported by Viidalepp (1996), but questioned by Hausmann & Viidalepp (2012). Hereby we confirm the occurrence of Triphosa sabaudiata in Turkey (see map).
DNA barcoding. The species clusters at low genetic distance with T. taochata (1.4%), diverging by more than 2% from T. silviae sp. n. (2.2%) and from T. lecerfi sp. n. (2.6%) (see table 2).
No known copyright restrictions apply. See Agosti, D., Egloff, W., 2009. Taxonomic information exchange and copyright: the Plazi approach. BMC Research Notes 2009, 2:53 for further explanation.
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Family |
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Genus |
Triphosa sabaudiata ( Duponchel, 1830 )
Wanke, Dominic, Hausmann, Axel & Rajaei, Hossein 2019 |
Triphosa agnata
Le Cerf 1918 |
Larentia millierata
Bruand 1855 |
Larentia sabaudiata
Duponchel 1830 |