Description of a new subgenus for Himalaeabatanga and its new sister species from Xizang Autonomous Region, China (Lepidoptera, Noctuidae, Amphipyrinae, Psaphidini)
EnyongChen‡, Alexey M.Prozorov§, AidasSaldaitis|, Roman V.Yakovlev§¶#, Günter C.Müller¤«, YonghongZhou‡
‡ Xizang University, Lhasa, China
§ Altai State University, Barnaul, Russia
| Nature Research Centre, Vilnius, Lithuania
¶ Tomsk State University, Tomsk, Russia
# Western Caspian University, Baku, Russia
¤ University of Sciences, Techniques and Technology of Bamako, Bamako, Mali
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Citation:
Chen E, Prozorov AM, Saldaitis A, Yakovlev RV, Müller GC, Zhou Y (2025) Description of a new subgenus for Himalaea batanga and its new sister species from Xizang Autonomous Region, China (Lepidoptera, Noctuidae, Amphipyrinae, Psaphidini). ZooKeys 1244: 293-303. https://doi.org/10.3897/zookeys.1244.154162
A new subgenus, Macrohimalaeasubgen. nov., in the genus Himalaea Hreblay & L. Ronkay, 1998, is established and described for Himalaea (Macrohimalaea) batanga Saldaitis, Benedek & Volynkin, 2022 and for a new species, Himalaea (Macrohimalaea) silvanasp. nov. This new species is the type of the new subgenus. The new subgenus is distinct from the nominotypical one in having antennal pectination and its forewing shape and male genitalia. All four known adult specimens of the genus and their genitalia are illustrated and compared. Their collection localities are mapped.
Key words:
Northeast Himalayan subalpine conifer forests ecoregion, Southeast Tibet shrublands and meadows ecoregion, systematics, taxonomy, Yarlung Zanbo arid steppe ecoregion
Introduction
The Qinghai-Xizang Plateau is a 2.5 million km2 area with an average altitude of 4000 m. The plateau was possibly elevated after the collision of the Indian and Asian continents about 50 My ago (Searle 2005), or more likely it is a result of much more complex processes originating during the Mesozoic Era (Spicer et al. 2020). The area includes three orogenic hotspots: the mountains of Central Asia, the Himalayas, and the mountains of Southwest China (Hengduanshan) (Mittermeier et al. 2011; Favre et al. 2014 also included part of Indo-Burma). The plateau and consists of more than 20 ecoregions (Olson et al. 2001). The genus Himalaea Hreblay & L. Ronkay, 1998, one of the region’s gems, belongs to the subtribe Psaphidina within the tribe Psaphidini of the subfamily Amphipyrinae (Wagner et al. 2008; Lafontaine and Schmidt 2010; Ronkay et al. 2011; Zahiri et al. 2011; Keegan et al. 2019, 2021; Rajaei et al. 2023). It was established for Himalaeaunica Hreblay & L. Ronkay, 1998, which was described based on a single adult male from Xizang (Tibet) Autonomous Region, China (Hreblay et al. 1998). The second species, Himalaeabatanga Saldaitis, Benedek & Volynkin, 2022, was also described from a single adult male but originated from the highlands of Sichuan Province, China (Saldaitis et al. 2022), about 850 km east of the type locality of H.unica. Himalaeabatanga differs from H.unica in having shorter antennal pectination, longer forewings, and different male genitalia, but the decision to consider it a separate subgenus was left until more comparative material was available. Recently, two adult males resembling H.batanga were collected in Xizang, about 530 km west of the H.batanga type locality, and based on differences in male genitalia they are considered a new species, described below. This new species, together with H.batanga, forms a group distinct from H.unica in both external appearance and male genitalia and is therefore considered to belong to a new subgenus, which is also established and described below.
Material and methods
Material
Adult moths deposited in the following collections were examined, photographed and dissected:
AFM – research collection of Alessandro Floriani (Milan, Italy);
HNHM – Hungarian Natural History Museum (Budapest, Hungary);
XU – Xizang University (Lhasa, China). Labels of adults are cited verbatim in quotation marks (“”), with lines separated by a slash (/).
Adults were photographed using an Olympus C7070CW, a Canon EOS 5D mark II with a Canon EF 100mm f/2.8L Macro IS USM lens, and a Canon EOS 5D Mark VI. Slides were photographed using the LEICA EZ4 W. All images were processed with Affinity Photo 2 and Affinity Publisher 2.
Genitalia dissection
Dissection was done following Hardwick (1950). The phallus was extracted and vesica was everted (Mikkola 2007; Zlatkov et al. 2022). The clasping apparatus and phallus were stained with Evans blue (Evans and Schulemann 1914; Cooksey 2013). The dissected genitalia were rinsed in 50%, 70%, and 96% ethanol and mounted on a microscope slide in Euparal (Gilson 1906; Neuhaus et al. 2017) and covered with a cover slip. Slides were deposited in the same collections as the dissected adults.
Himalaea
Hreblay & L. Ronkay in Hreblay et al. 1998: 135. Type species: Himalaeaunica Hreblay & L. Ronkay, 1998, by original designation.
Diagnosis.
Adult males have bipectinate antennae and brownish-grey coloration. The main diagnostic feature in the clasping apparatus is an enlarged outgrown ampulla (digitus sensu Saldaitis et al. 2022), whereas the ampulla of other Psaphidini, if present, is smaller and does not rise above the surface of the valva. The vesica has anterior and posterior elasmas at the base of the vesica ejaculatorius, which are flat, sclerotized plates or raised, volumetric, sclerotized plates with serrated surfaces. Elasma occur in some other genera of Psaphidini: Valeria Stephens, 1829, Meganephria Hübner, 1820, Benedekia Ronkay, Ronkay, Gyulai & Hacker, 2010, and Allophyes Tams, 1942; however, the combination of robust ampulla and both anterior and posterior elasmas are unique within the tribe.
Taxonomic synopsis
Subgenus Himalaea Hreblay & L. Ronkay, 1998
Himalaea (Himalaea) unica Hreblay & L. Ronkay, 1998
Subgenus Macrohimalaea subgen. nov.
Himalaea (Macrohimalaea) batanga Saldaitis, Benedek & Volynkin, 2022, stat. nov.
Himalaea (Macrohimalaea) silvana sp. nov., here designated.
Diagnosis.
The new subgenus differs from the nominotypical one in having shorter rami, and 1.3–1.5 times longer forewings with tapered apices (compare Fig. 1 with Figs 2–4). The male genitalia have an even-surfaced anellus, a dorsad elongated juxta, a sclerotized costa reaching the apex of the cucullus, a less-sclerotized ampulla lacking a harpe, an unpronounced carina, larger dorsal diverticulum bearing cornuti, and flat anterior elasma (compare Fig. 5 with Figs 6–8).
Adult male (Figs 2–4). Antenna bipectinate, rami gradually elongating towards mid third of antenna and then gradually shortening in distal third. Head, thorax, and abdomen dorsally brown-mottled, abdomen dark brown to blackish brown. Forewing 23.3 mm long; somewhat triangular, elongate and relatively narrow with obtuse tornal angle, slightly crenulate outer margin, prominence at M3, and tapered apex. Pattern consists of basal, medial, subterminal and terminal fields, with subterminal field being the lightest; dark basal streak within claviform spot bordered with dark wavy antemedial line; orbicular spot a little smaller than reniform spot, both with dark contour; dark, crenulate postmedial line; blurred, dark streak from posterior margin of reniform spot towards apex of wing; blurred, dark, zigzag subterminal line; more or less pronounced dark tornal streak; and dark terminal line split interrupted at veins. Cilia brown-mottled. Hindwing somewhat triangular with rounded apex and slightly crenulated outer margin; light-colored, getting darker at distal margin of discal cell. Cilia brown-mottled. Male genitalia (Figs 6–8). Uncus somewhat digitiform, basally bent at around 90°, apically narrowed to pointed apex. Tegumen a band narrowing towards connection with vinculum. Vinculum somewhat longer than tegumen, ventrally forming U-shaped saccus. Valva elongate, about the size of tegumen-vinculum complex, with well-pronounced sclerotized costa and sacculus, membrane between them, and membranous valvula, all sparsely covered with setae; distal third of costa less sclerotized, medially connected with relatively short (in comparison to Himalaea) editum bearing ampulla; sacculus narrowing towards barely protruded rounded distal apex; both valvae joint with tendon. Juxta an elongated plate narrowing distally. Anellus small with smooth surface. Phallus as long as valva, slightly bent medially, with elongate coecum and wide entrance of ductus ejaculatorius; vesica somewhat conical, downcurved, with dorsal spherical diverticulum bearing three or four cornuti; at base of vesica ejaculatorius, anterior elasma flat, posterior elasma may be raised or flat. Adult female unknown.
Etymology.
The name Macrohimalaea is a derivative from Himalaea, the type subgenus of the genus, and prefix macro- for big or large to indicate that the specimens of Macrohimalaea are larger than the ones of Himalaea.
Holotype: • 1 male, “TU-01084/ At the junction of Bahe Town (Gongbu Jiangda County) and Baiba Town (Bayi District) / Baiba Town / Bayi District, Linzhi City, / Xizang / N 29° 52’ 22.09” / E 92° 31’ 31.96” / 23.8.2004 h 4203.7m (coll. XU),” GS prepared by Chen Enyong (XU).
Paratype: • 1 male, same data but “TU-01083” (XU).
Diagnosis.
The new species differs from H. (M.) batanga in having thicker rami, less contrasting forewings, and slightly darker hindwings (compare Figs 3, 4 with Fig. 2). The male genitalia which are lacking a clavus have wider ampulla, an unprotruded costa, a downcurved phallus, cornuti at the top of the dorsal diverticulum, and flat posterior elasma (compare Figs 3, 4 with Fig. 2). The new species was collected within the Northeast Himalayan subalpine coniferous forest ecoregion, which contrasts with H. (M.) batanga, which was collected within the Southeast Tibet shrublands and meadows.
Description.
Male (Figs 3, 4). Antenna bipectinate, rami gradually elongating towards mid third of antenna and then gradually shortening in distal third. Flagellum covered with greyish scales. Head dorsally, patagium and tegula grey-mottled. Thorax dorsally dark grey-mottled. Abdomen dorsally greyish-brown mottled at tergites II to III and at distal tip, whereas tergites IV to VIII covered with blackish scales. Forewing 23.3 mm long; somewhat triangular, elongate and relatively narrow with obtuse tornal angle, slightly crenulate outer margin, prominence at M3, and tapered apex. Pattern consist of greyish-brown mottled basal, medial, subterminal and terminal fields, with subterminal field being the lightest; dark-brown, narrow, basal streak inside light-greyish-brown claviform spot bordered with dark-brown, wavy antemedial line; orbicular and reniform spots with light-brown and sparse dark-brown scales and dark-brown contour; dark-brown, crenulate postmedial line; blurred, dark-brown streak from posterior margin of reniform spot towards apex of wing; blurred, dark-brown, zigzag subterminal line with whitish posterior streaks; more or less pronounced dark-brown tornal streak; and blackish terminal line interrupted at veins. Cilia greyish-brown mottled. Hindwing somewhat triangular with rounded apex and slightly crenulated outer margin. Light brown, getting darker at distal margin of discal cell and towards outer margin. Cilia brown-mottled. Male genitalia (Figs 7, 8). Uncus somewhat digitiform, basally bent at around 90°, apically narrowed to pointed apex. Tegumen a band narrowing towards connection with vinculum. Vinculum somewhat longer than tegumen, ventrally forms U-shaped saccus. Valva elongate, about the size of tegumen–vinculum complex, with well-pronounced sclerotized costa and sacculus, membrane between them, and membranous valvula, all sparsely covered with setae; distal third of costa less sclerotized, medially connected with rather short editum bearing somewhat trapezoidal ampulla with wavy distal margin and two lateral rounded apices, posterior one two times longer than anterior one; sacculus narrowing towards barely protruded rounded distal apex; both valvae joint with tendon. Juxta an elongated, distally narrowing plate. Anellus small, with smooth surface. Phallus as long as valva, slightly downcurved medially, with elongate coecum and wide entrance of ductus ejaculatorius; vesica somewhat conical, downcurved, with dorsal spherical diverticulum distally bearing three or four aligned cornuti, two elasmas pronounced at base of vesica ejaculatorius: anterior one somewhat oval, with fuzzy margin, weakly sclerotized (Fig. 8), and posterior one somewhat oval or heart-shaped with well-pronounced proximal margin and fuzzy distal margin, sclerotized harder than anterior one. Female unknown.
Biology and distribution (Figs 9–11).
The type series was collected from an altitude of 3,200 m on 23 August between 21:10 p.m. and 1:20 a.m. when the temperature was 15–16 °C and the relative humidity was around 60%. Adult moths collected there belonged to the families Noctuidae, Geometridae, Lasiocampidae, and Cossidae, with Noctuidae dominating in both numbers of species and individuals. The collection site was at the bottom of an alpine valley where the plant community was primarily dominated by Pinusdensata and Quercusaquifolioides, while the main plant community at the valley floor consisted of small shrubs. The collecting site lies within the Northeast Himalayan subalpine coniferous forest ecoregion.
The name silvana is a feminine derivative from the Latin noun silva meaning forest, given to the species for its occurrence near the Northeast Himalayan subalpine coniferous forest.
Acknowledgements
We express our sincere thanks to the Key Laboratory of Biodiversity and Environment on the Qinghai-Xizang Plateau (Ministry of Education), the Yani Wetland Ecosystem Positioning Observation and Research Station, and the Key Laboratory of Forest Ecology in Xizang Plateau (Ministry of Education). We also thank Balázs Tóth (HNHM, Budapest, Hungary) for photos of the holotype of Himalaeaunica. We are also indebted to János Babics (Budapest Hungary) for genitalia preparation of the HT of H.batanga and to Balázs Benedek (Mohács, Hungary) for valuable advices. We express our gratitude to Robert Borth for careful check of the manuscript, as well as to Kevin Keegan, Péter Gyulai, and two other reviewers of the manuscript for their time and care.
Additional information
Conflict of interest
The authors have declared that no competing interests exist.
Ethical statement
No ethical statement was reported.
Use of AI
No use of AI was reported.
Funding
The work of Enyong Chen and Yonghong Zhou was supported by Science and Technology Projects of Xizang Autonomous Region, China (XZ202402ZD0005), as well as a project from the Science and Technology Bureau of Nagqu City (GZFCG2024-21707), and the Key R&D Project of Science and Technology Program of Xizang Autonomous Region (Grant No. XZ202501ZY0091).
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