Lemonia levantina, Prozorov & Prozorova & Volkova & Yakovlev & Saldaitis & Ortiz & Bianco & Schneider & Revay & Müller, 2022

Prozorov, Alexey M., Prozorova, Tatiana A., Volkova, Julia S., Yakovlev, Roman V., Saldaitis, Aidas, Ortiz, Antonio S., Bianco, Giovanni, Schneider, Tom, Revay, Edita E. & Müller, Günter C., 2022, Description of a new Middle Eastern Lemonia species, comments on the Lemonia philopalus complex and Lemonia syriensis (Lepidoptera: Brahmaeidae: Lemoniinae), Ecologica Montenegrina 57, pp. 77-97 : 88-91

publication ID

https://doi.org/ 10.37828/em.2022.57.8

publication LSID

urn:lsid:zoobank.org:pub:DF78B3FB-7901-4181-9C84-F85DA02CD5E6

persistent identifier

https://treatment.plazi.org/id/45B280B0-4A54-481B-9ADE-3A966A56D6F5

taxon LSID

lsid:zoobank.org:act:45B280B0-4A54-481B-9ADE-3A966A56D6F5

treatment provided by

Felipe

scientific name

Lemonia levantina
status

sp. nov.

Lemonia levantina sp. n.

http://zoobank.org/ urn:lsid:zoobank.org:pub:DF78B3FB-7901-4181-9C84-F85DA02CD5E6

( Figs 1–3 View Figures 1–6 , 7 View Figures 7–8 , 15–16 View Figures 9–16 , 33–38 View Figures 28–38 , 61–65 View Figures 58–71 , 77–79 View Figures 77–79 )

Type material: HOLOTYPE ♂, Jordan , Rift Valley, 40 km N of Aqaba, sands NW Rahma, ca. 100 m, leg. G. Müller & E. Revay ( ZSM) . PARATYPES (195♂, 22♀ total; all CGM): Egypt : 36♂, 4♀, SW Sinai, 30 km E of Abu Zenima , edge of sand dunes, contacted semi-shrub vegetation, 500 m, 25.I –5.II.1996, 28.I – 12.II.1998, 5–17.II.1999, leg. G. Müller ; 4♂, ♀, S Sinai, near Sharm El-Sheikh , 200 m, II.2002, I.2009, leg. V. Kravchenko & G. Müller ; ♂, S Sinai, Saint Catherine , ca. 1800 m, 5–20.XI.2002, leg. G. Müller ; ♂, S Sinai, Saint Catherine , ca. 500 m, I.2002, I.2003, leg. G. Müller ; ♂, Sinai, Abu Darbah, I.2002, leg. G. Müller ; ♂, ♀, Sinai, Dahab , ca. 200 m, I.2002, leg. G. Müller ; 3♂, ♀, East Coast, Jebel Hamafah , ca. 800 m, 5–12.XII.2002, leg. V. Kravchenko & G. Müller ; 2♂, Eastern Desert, Sudan border, Jebel Hamatha , ca. 800 m, II.2003, leg. V. Kravchenko & G. Müller ; 2♂, Eastern Desert, Ras Garib City , 50 m, XI.2002, leg. G. Müller ; ♂, Jabal al ‘ Urf , 900 m, I.2003, leg. G. Müller ; 4♂, Zaafarana , 500 m, I.2003, leg. G. Müller ; ♂, Hurghada, Jebel Abu Harbak, 800–1200 m, XI.2002 – I.2003, leg. G. Müller ; ♂, Bir- Abraq , 23.35° N, 34.48° E, 1100–1400 m, 29.XII.2008, leg. Evans. GoogleMaps Gaza Strip: 5♂, near Rafah , ca. 500 m, 12.I.2001, leg. G. Müller ; 2♂, Beit Hanoun , 500 m, 10–20.I.2002, leg. V. Kravchenko & G. Müller ; 5♂, South Gaza Strip , ca. 50 m, XII.2001, leg. G. Müller. Israel: 10♂, ♀, Western Negev , ca. 200 m, I.2003, leg. G. Müller ; ♂, Negev, Holot ` Agur , II.2002, leg. V. Kravchenko & G. Müller ; 7♂, Arad , 500–600 m, XII.2001, I.2002, II.2002, I.2003, leg. G. Müller ; 21♂, 2♀, Samar , ca. 100 m, 15.II.1985, 12–17.II.1988, II.2009, leg. G. Müller ; 9♂, Southern Arava valley, near Grofit , ca. 150 m, II.2010, leg. V. Kravchenko & G. Müller ; 3♂, Grofit , ca. 150 m, 8.II.1987, leg. G. Müller ; 3♂, Southern Arava, Grofit , ca. 150 m, 3.II.2000, 6.II.2000, leg. G. Müller ; 9♂, Southern Arava Valley, near Grofit , ca. 150 m, II.2000, leg. V. Kravchenko & G. Müller ; ♂, SW Negev, Nahal Pehami , 2.II.2000, leg. G. Müller ; 5♂, sands N Eilat , II.1989, leg. G. Müller ; 2♂, 15 km N Eilat , I.2003, leg. G. Müller. Jordan: 18♂, ♀, Rift Valley , 40 km N of Aqaba, sands NW Rahma, ca. 100 m, leg. G. Müller & E. Revay ; 10♂, ♀, Rift Valley , 90 km N of Aqaba, sands SW Ar-Rishah, ca. 100 m, leg. G. Müller & E. Revay ; ♂, Halat Ammar , ca. 900 m, I.2002, leg. G. Müller ; ♂, Al- Jafr , ca. 900 m, I.2002, leg. G. Müller ; ♂, Aqaba, ca. 100 m, II.2002, leg. G. Müller ; ♂, 50 km N Amman, Al Maidal , 1000 m, 25–30 I.2002, leg. G. Müller , BC JM 0055. Iraq: 10♂, Ad Nadhatah , ca. 600 m, I.2003, leg. G. Müller ; 1♂, Wadi Muhammadi , ca. 300 m, I.2003, leg. G. Müller. Saudi Arabia: 7♂, 3♀, Al Bid' , ca. 400 m, II.2004, leg. G. Müller ; 5♂, 2♀, Rijal , ca. 1500 m, 1–10.II.2002, leg. G. Müller ; ♂, Jabal Buwarah , ca. 1200 m, XII.2001, leg. G. Müller ; ♂, Alflumaydah , ca. 100 m, II.2002, leg. G. Müller.

Diagnosis. Levantine-Egyptian species, it has a 4.86% genetic distance from the Moroccan L. philopalus rungsi and 5.55% from the Iberian L. vazquezi ( Figs 77–78 View Figures 77–79 ). Externally and morphologically variable, no reliable character found to distinguish it from the sister species. Worn specimens may be confused with the sympatric Lemonia syriensis Daniel, 1953 ( Figs 39–53 View Figures 39–53 ), but generally the coloration of L. levantina sp. n. is darker and more contrasting, cilia paler, forewings narrower (see Figs 34 View Figures 28–38 and 45 View Figures 39–53 ); uncus usually with well pronounced isthmus (see Figs 64 and 70 View Figures 58–71 ); imagoes occur in sandy desert areas instead of grasslands ( Figs 79–81 View Figures 77–79 View Figures 80–82 ).

Description. Male habitus. Antenna brown, pectination elongates within the first sixth of the antenna length and stays the same length until the distal 1/6 th where it quickly shortens. Flagellum tripectinate – each flagellomere bears a pair of opposite ventral lateral elongated rami and a single short medial ramus on the ventral side, all three densely covered with sensilla ( Figs 1–2 View Figures 1–6 ). Maxillary palpi very small ( Fig. 1 View Figures 1–6 ); labial palpi three-segmented ( Fig. 3 View Figures 1–6 ). Venation similar to other Lemonia species ( Figs 7–8 View Figures 7–8 ). Forewing length: 18– 25 mm; wingspan: 40–49 mm. Background coloration brown, veins creamy. Cilia creamy. Discal spot a creamy torus on outer margin of cell. External field may be pale ( Fig. 33 View Figures 28–38 ) or of background color ( Fig. 34 View Figures 28–38 ), external line of pale color, more or less pronounced. Hindwing follows the same coloration as forewing but without discal spot, may be completely pale ( Fig. 33 View Figures 28–38 ) or with lighter medial field ( Fig. 34 View Figures 28–38 ). Cilia creamy. Abdomen dorsally dark brown with creamy interspace between abdominal segments, ventrally creamy. Femur yellow and tibia creamy, tarsi black and creamy. The tibial spur formula is 0-2-2, epiphysis absent ( Figs 15–16 View Figures 9–16 ). Foreleg’s basitarsus bears 2–3 big spurs, second tarsomere may bear one big spur, distitarsus apically bears a pair of long chaetae. Male genitalia ( Figs 61–65 View Figures 58–71 ). Tegumen somewhat triangular, widening basally. Socii membranous, covered with short chaetae. Uncus elongated, apically may be rounded ( Fig. 64 View Figures 58–71 ) or pointed ( Fig. 65 View Figures 58–71 ), varies in width and length with more or less pronounced isthmus near its base, covered with short chaetae. Gnathos short, rounded, spatula-like with uneven surface, narrow subanal plate going from it towards anal opening. Vinculum narrow, band-like. Valvae elongated, rounded, covered with chaetae, ventral lateral margin more or less convex ( Figs 64–65 View Figures 58–71 ); sacculus weakly pronounced. Juxta boat-like, apically rounded, widened basally, surrounds aedeagus. Aedeagus elongated, narrow, c-shaped. Vesica small, bag-shaped. The eighth sternum small, somewhat triangular, apically rounded, varies in shape. The eighth tergum trapezoid not modified. Female habitus similar to male ( Figs 36, 38 View Figures 28–38 ), but larger in size, antenna pectination shorter, discal spot less pronounced if at all. Forewing length: 26–28 mm; wingspan: 48– 55 mm. Female genitalia have not been studied.

Etymology. We dedicate the subspecies to the region of the Levant where the species was predominantly collected.

Distribution ( Fig. 77 View Figures 77–79 ). Mainly arid, sandy areas in North East and South East Egypt, Southern Israel, Jordan, Northern Iraq and Northwestern Saudi Arabia.

Biology ( Fig. 79 View Figures 77–79 ). The new species is found in semidesert and desert habitats with annual precipitation below 300 mm. The psammophilous taxon inhabits areas with sparse and scattered vegetation. It occurs mainly on lowland with a few records in SE Egypt above 1000 m, here it is restricted to water catchments in hyper-arid environment. Adults were collected from late November to mid-February with a clear peak from late December to February. The higher the altitude, the earlier adults can be found. It is worthwhile mentioning that the flight period of single populations does not exceed two weeks. The new taxon can be regarded as a late winter – early spring species. In contrast the Western taxa appear to fly mainly in autumn and are found in open and forested Mediterranean grassland habitats, to our best knowledge there are no records from desert habitats.

The early stages of the new taxon are unknown, but the caterpillars are probably night active and feed on low herbaceous plants. The new species is very local, rare and almost the complete material was collected with long-term operated light traps within two decades. Adults appear mainly after midnight until sunrise to light sources, typically at very low temperatures.

ZSM

Bavarian State Collection of Zoology

Kingdom

Animalia

Phylum

Arthropoda

Class

Insecta

Order

Lepidoptera

Family

Brahmaeidae

Genus

Lemonia

Darwin Core Archive (for parent article) View in SIBiLS Plain XML RDF