Bachmarima expansa, Constant & Pham, 2025
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publication ID |
https://doi.org/10.5852/ejt.2025.1025.3101 |
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publication LSID |
lsid:zoobank.org:pub:CE878E69-7345-43E7-AB8F-1B99FC89F710 |
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DOI |
https://doi.org/10.5281/zenodo.17724218 |
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persistent identifier |
https://treatment.plazi.org/id/03F687C3-FFE0-0A00-FDAC-A484FABC6AFF |
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treatment provided by |
Plazi |
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scientific name |
Bachmarima expansa |
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gen. et sp. nov. |
Bachmarima expansa gen. et sp. nov.
urn:lsid:zoobank.org:act:
Figs 1–5
Diagnosis
Bachmarima expansa gen. et sp. nov. can be recognized by (1) the moderately elongate lateroventral processes of the aedeagus, reaching midlength of the aedeagus ( lvp – Figs 3E–L, 4D–F); (2) the dorsal lobe of the periandrium strongly expanded into a lamina lateroventrally and with lateral margins rounded in basal portion in dorsal view ( dl – Figs 3E–L, 4A).
Differential diagnosis
The new species is close to Bachmarima recta gen. et sp. nov. and Bachmarima valida gen. et sp. nov. but B. recta shows much longer lateroventral processes of the aedeagus ( lvp – Fig. 8D–F), reaching near base of the aedeagus sensu stricto (only reaching midlength in B. expansa : lvp – Fig. 4D–F), while in B. valida , the process reaches only the distal ⅓ of aedeagus ( lvp – Fig. 12D–F).
Etymology
The species epithet ‘ expansa ’ is a Latin adjective meaning ‘expanded’; it refers to the dorsal lobe of the periandrium distinctly, roundly expanded lateroventrally in this species.
Type material
Holotype
VIETNAM • ♂; Th ừa Thiên-Huế Province, Bach Ma National Park; 16°13′38″ N, 107°51′20″ E; 500– 600 m a.s.l.; 10–20 May 2023; J. Constant and L. Semeraro leg.; pheasant trail; VNMN. GoogleMaps
Paratypes
VIETNAM – Th ừa Thiên-Huế Province • 4 ♂♂; same data as for holotype; VNMN GoogleMaps • 8 ♂♂; same data as for holotype; I.G.: 34.640; RBINS GoogleMaps • 3 ♂♂; Bach Ma National Park ; 16°13′38″ N, 107°51′20″ E; 350–600 m a.s.l.; 18 Oct. 2024; J. Constant, L. Semeraro and T. T. H. Nguyen leg.; pheasant trail; I.G.: 34.893; RBINS GoogleMaps • 4 ♂♂; Bach Ma National Park ; [ 16°13′38″ N, 107°51′20″ E]; 289 m a.s.l.; 29 May 2023; pheasant trail; T. T. H. Nguyen leg.; VNMN GoogleMaps • 6 ♂♂; Bach Ma National Park , near ranger station; 16°08′37″ N, 107°49′36″ E; 300–600 m a.s.l.; 18 May 2023; J. Constant and L. Semeraro leg.; I.G.: 34.640; RBINS GoogleMaps • 5 ♂♂; same data as for preceding; VNMN GoogleMaps • 5 ♂♂; Bach Ma National Park, Nam Dong District , ranger station; 16°08′37″ N, 107°49′36″ E; 150–500 m a.s.l.; 19 Oct. 2024; J. Constant, L. Semeraro and T. T. H. Nguyen leg.; I.G.: 34.640; RBINS GoogleMaps • 4 ♂♂; same data as for preceding; VNMN GoogleMaps • 1 ♂; Bach Ma National Park, Yes Hue Eco ; 16°13′05″ N, 107°43′27″ E; 200–300 m a.s.l.; 17 May 2023; J. Constant and L. Semeraro leg.; I.G.: 34.640; RBINS GoogleMaps • 1 ♂; Bach Ma National Park ; 16°11′44″ N, 107°50′44″ E; 1200–1300 m a.s.l.; 22 May 2023; J. Constant and L. Semeraro leg.; roadside; I.G.: 34.640; RBINS GoogleMaps • 1 ♂; Bach Ma National Park ; 30 May 2023; T. T. H. Nguyen leg.; summit trail; light trap; VNMN • 1 ♂; same data as for preceding; [by] net; VNMN • 2 ♂♂; Bach Ma National Park ; 15 Mar. 2023; V. T. Trung leg.; VNMN • 2 ♂♂; Th ừa Thiên-Huế Province, Bach Ma National Park , road to Bach Ma Peak ; 16°11′45.73″ N, 107°51′46.34″ E; 1325 m a.s.l.; 14 Sept. 2024; T. T. H. Nguyen leg.; [by] net; AU00657 and AU00658; VNMN GoogleMaps • 1 ♂; Phong Dien District ; 16°30′27″ N, 107°16′05″ E; 350–400 m a.s.l.; 23 May 2023; J. Constant and L. Semeraro leg.; I.G.: 34.640; RBINS GoogleMaps • 2 ♂♂; same data as for preceding; VNMN GoogleMaps .
Description
MEASUREMENTS AND RATIOS. LT: ♂ (n = 10): 5.7 mm (5.5–5.9); LT/BB = 1.94; LTg/BTg = 2.20; LW/BW = 1.23; BV/LV = 2.23; LF/BF = 0.85.
HEAD ( Fig. 1A–E). Vertex brown, often with paler marking on each side and obsolete median carina yellowish; 2.2 × as broad as long in midline, slightly constricted in middle; disc weakly concave; anterior margin slightly, angularly projecting anteriad; posterior margin rather deeply concave; all margins moderately carinate. Frons brown, weakly convex, smooth with distinct, strongly curved yellow marking on each side of complete median carina, sometimes more or less merging together on carina, and obsolete peridiscal carina marked with yellowish (mostly in dorsal portion of frons); yellow marking along fronto-clypeal suture, wider in middle. Genae yellowish brown with anteroventral angle slightly projecting anteriad. Clypeus triangular, convex, smooth, not keeled or carinate; anteclypeus brown with sides yellowish; postclypeus blackish brown. Labium brown with last segment longer than broad, shorter than penultimate. Antennae with scape short, ring-shaped, yellowish, and pedicel bulbous, yellowish with basal ⅓ brown.
THORAX ( Fig. 1A, C–E). Pronotum brown with paler, yellowish median line, more visible in anterior portion; subtriangular, projecting anteriorly; smooth with anterior margin carinate and pair of impressed points on each side of midline; lateral fields very narrow behind eyes; paranotal lobes brown, yellowish under eye and with black marking along ventral margin; posteroventral angle rounded. Mesonotum brown, often with carinae marked with yellowish, smooth, weakly convex with shallow depression before scutellum sometimes containing obsolete median carina; sublateral (peridiscal) carinae incomplete but rather distinct. Tegulae yellowish brown.
TEGMINA ( Figs 1A–D, 2A–B, 4). Brown with main veins slightly darker, elevated, and cross-veins weakly raised and darker, or paler along costal margin; often with zigzaged marking of white wax more or less following claval joint with posterior branch reaching MP vein, and transverse marking subapically; distinctly convex, and about 2.2 × as long as wide, with distinct lateral hump including vein ScP+RA slightly before basal ⅓; rather narrow but distinct, yellowish epipleuron; clavus closed, reaching 4 /5 of tegmen length. Venation as in genus description.
HIND WINGS ( Fig. 1F). Blackish brown; veins generally black, darker than background; well developed, with three distinct lobes ( Sarimini type) more or less equal in width; indentation between ScP-R-MP-Cu and Pcu-A1 lobes moderately deep. Venation as in genus description.
LEGS ( Figs 1A–E, 2C–D). Yellowish brown, paler than tegmina; distal portion of metafemora and basal portion of metatibiae darkened; all spines of posterior legs black apically. Anterior and median legs slightly flattened dorsoventrally, tibiae more slender than corresponding femora; posteroventral margin of pro- and mesofemora with row of minute teeth in distal portion; pro- and mesotarsi rather elongate. Metatibiae with two lateral spines in distal half, and seven apical spines. Metatarsi rather short with first segment about as long as combined length of remaining segments. First metatarsomere with two latero-apical and 7 intermediate spines arranged in arc. Metatibiotarsal formula: (2) 7/ 9/ 2.
ABDOMEN ( Fig. 1B). Brown with median area darker.
MALE TERMINALIA ( Figs 3–4). Pygofer ( Py – Fig. 3A–D) short, about 2.4 × as high as long at midheight in lateral view, with posterior margin broadly rounded in lateral view; in caudal view suboval, 1.3 × as high as wide; dorsally abruptly, deeply notched. Gonostyli ( G – Fig. 3A–D) massive, moderately convex, with anterodorsal margin rounded, then abruptly sinuate at base of capitulum; ventral margin rounded; posterior margin roundly projecting caudad in lateral view and sinuate towards base of capitulum; capitulum ( ca – Fig. 3A–B, D) elongate, digitiform, strongly projecting dorsad and with poorly distinct neck, curved anterodorsad and evenly tapering towards apex in lateral view, in caudal view slightly directed mesad and with basilateral laminate process directed lateroventrad. Anal tube ( An – Fig. 3A–D) elongate, dorsoventrally flattened, and sublanceolate, weakly grooved medially beyond anal opening (in basal ¼), rather narrow, about 2.8 × as long as wide in dorsal view; in lateral view abruptly narrowing at anal opening, then weakly downcurved. Aedeagus ( ae – Figs 3E–L, 4) symmetrical, curved posterodorsad in lateral view. Ventral lobe of periandrium ( vl – Figs 3G–I, K–L, 4A–C) laminate, spatulate with apical margin rounded, shorter and much narrower than dorsal lobe. Dorsal lobe of periandrium ( dl – Figs 3E– L, 4A–C, G) strongly expanded into lamina lateroventrally, with sides rounded in dorsal view in proximal portion, then sinuately, strongly tapering towards truncate apex, lamina covering distal portion of lateroventral processes of aedeagus; laterodorsal processes of periandrium ( ldp – Figs 3E–F, I, 4A–C, G) pointed and curved towards the posterior and with lateral tooth. Aedeagus (sensu stricto, ae – Figs 3E–L, 4D–F) surpassing dorsal and ventral lobes of periandrium, bifid, each shaft widening distally to obliquely truncate apex; robust lateroventral processes ( lvp – Figs 3E–L, 4D–F) arising subapically, weakly curved ventrocephalad and (in caudal view) slightly sinuate, reaching to midlength of aedeagus. Connective ( co – Fig. 3G) well developed, corpus connective long, regularly curved in lateral view, tectiductus ( te – Fig. 3G) well developed, conical with anteroventral apodemes and wide anterior foramen.
Biology
Bachmarima expansa gen. et sp. nov. was collected in the months of March, May, September and October at altitudes between 150 and 1325 m a.s.l., in moist evergreen tropical forest. The specimens were sitting on small branches and leaves, on lower vegetation, bushes and trees. In Bach Ma National Park, it was found at the following collecting site/habitats ( Constant & Pham 2025a: fig. 2a): “Yes Hue Eco” ( Constant & Pham 2025a: fig. 2a(1), b), “pheasant trail” ( Constant & Pham 2025a: figs 2a(2), 3a), “roadside” ( Constant & Pham 2025a: figs 2a(4), 4a), “summit” ( Constant & Pham 2025a: figs 2a(5), 4b) and “ranger station” ( Constant & Pham 2025a: figs 2a(6), 5a), and in Phong Dien district ( Constant & Pham 2025a: fig. 5b).
Distribution
Vietnam: Thừa Thiên-Huế Province, Bach Ma National Park and Phong Dien District ( Fig. 4H).
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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