Sabactiopus schuhi, Yasunaga, 2024

Yasunaga, Tomohide, 2024, New genera and species of the ‘ Lygus-complex’ ranging from the Himalaya-Oriental to the Wallacea region (Insecta: Heteroptera: Miridae: Mirinae), Raffles Bulletin of Zoology 72, pp. 371-423 : 416-422

publication ID

https://doi.org/10.26107/RBZ-2024-0030

publication LSID

lsid:zoobank.org:pub:1F1754CC-6835-4B66-AB5C-FA22AC85D481

persistent identifier

https://treatment.plazi.org/id/03B2879F-FF90-3B3D-1583-FC72FEF0FBC7

treatment provided by

Felipe

scientific name

Sabactiopus schuhi
status

sp. nov.

Sabactiopus schuhi , new species

( Figs. 7 View Fig G−J, 18A–G, 34J–L, 35A−I)

Type material. Holotype: male, NEPAL: Kathmandu Valley : Lalitpur , Godawari, Mt. Pulchoki (1,500–1,800 m), 27°34′45″N, 85°22′44″E, on Urtica dioica, T. Yasunaga , 2 August 2006 ( NMTU) ( AMNH _ PBI 378790 About AMNH ) GoogleMaps . Paratypes: NEPAL: 1 female, same data as for holotype ( TYCN); Kaski: Pokhara, Begnas Lakeside, 28°10′N 84°06′E, T GoogleMaps . Yasunaga, 6 November 2005 ( NMTU). THAILAND: 1 male, Doi Suthep, Chiang Khian, 850 m alt., 18°50′N 98°54′E, S. Nagashima, 15 August 2001 ( DOAT) GoogleMaps .

Diagnosis. Being closely related to S. sauteri (Poppius) , S. schuhi , new species can be distinguished by smaller size; narrower vertex; wider yellowish subbasal annulation on antennal antennomere II; antennomere III longer than IV; roundly inflated sensory lobe of left paramere; T-shaped apex of right paramere; anchor-shaped apex and roundly inflated sensory lobe of left paramere; narrowed sclerotised rings; and mesally separated interramal lobes, in addition to being associated with a herb from the Urticaceae , Urtica dioica .

Description. Body ovoid, stout, rather box-like, small-sized; in female body larger and paler in colour ( Fig. 7G–I View Fig ); basic colouration shiny dark reddish brown; dorsum polished, finely and sparsely punctate, with uniformly distributed, pale, simple, reclining or semi-erect setae on mesoscutum, scutellum and hemelytra. Head shiny pale brown, partly tinged with red, almost glabrous; eyes small; basal transverse carina on vertex with several upright setae, about as thick as pronotal collar ( Fig. 34K View Fig ). Antenna dark brown; antennomere I with darkened apex, base and middle; antennomere II with pale ring at basal ⅓, as long as or slightly shorter than basal width of pronotum; base of antennomere III whitish, longer than IV. Labium pale brown, reaching but not exceeding apex of metacoxa; segment IV reddish brown. Pronotum shiny pale or reddish brown, shallowly punctate or rugose, almost glabrous ( Fig. 29K View Fig ); calli sometimes with a pair of dark spots, flat; pleura pale brown; metathoracic scent efferent system greyish brown, with rather flat peritreme ( Fig. 35A View Fig ); scutellum shiny fuscous, with creamy V-shaped margin. Hemelytron shining, pale brown or reddish brown, widely darkened posteriorly, declivous at cuneal fracture; cuneus yellowish brown apically, with dark apex; membrane pale smoky brown. Coxae and legs pale brown, partly tinged with red; meso- and metacoxa, and base of each femur more or less darkened; tibiae with dark spots or annulations at bases of pale brown spines; tarsomere III darkened; meta-tarsomere II as long as III; pretarsal structures as in Fig. 30C View Fig . Abdomen fuscous; female sterna VII–IX pale brown. Male genitalia ( Figs. 18A–D View Fig , 35 View Fig D−F): Left paramere with roundly inflated sensory lobe ( Figs. 30D View Fig ); right paramere with elongate hypophysis and T-shaped, flat apex ( Figs. 18C View Fig , 35E View Fig ). Vesica widely membranous, with two lobal-sclerites, one of which is deeply notched; secondary gonopore thick-rimmed ( Figs. 18D View Fig , 35F View Fig ). Female genitalia ( Figs. 18E–G View Fig , 35 View Fig G−I): Genital chamber with small, narrow sclerotised rings that are separated to each other ( Fig. 35G View Fig ); posterior wall lacking dorsal structure or lateral lobe; interramal lobe comparatively narrow, densely covered with spinules ( Fig. 35I View Fig ), each lobe separated mesally ( Fig. 35H View Fig ).

Measurements. See Table 1.

Etymology. Named in honour of Dr. Randall T. Schuh (Curator Emeritus, AMNH), one of the world’s most prominent heteropterists and my long-time mentor; an adjective.

Distribution. Nepal (Kathmandu Valley, Kasuki), Thailand (Chiang Mai).

Biology. In Kathmandu Valley, several adults of this new species were found to inhabit Urtica dioica L. ( Urticaceae ) and to coexist on the herb with Himalisundacoris duwalae under deciduous/evergreen mixed broadleaf forest ( Fig. 7J View Fig ). On the other hand, the Taiwanese congener, S. sauteri (Poppius) , has been collected from the inflorescences and flower-buds of broadleaf trees, such as Styrax formosanus Matsum. ( Styracaceae ) ( Fig. 7L View Fig ). Chérot et al. (2017) reported that a Papua New Guinean congener, S. zhengi Chérot, Gorczyca, Schwartz & Demol, 2017 , was collected by canopy-fogging.

AMNH

American Museum of Natural History

T

Tavera, Department of Geology and Geophysics

Kingdom

Animalia

Phylum

Arthropoda

Class

Insecta

Order

Hemiptera

Family

Miridae

Genus

Sabactiopus

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