Biodiversity Data Journal :
Taxonomic Paper
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Corresponding author: Kyosuke Okuda (kyskokuda@gmail.com)
Academic editor: Laurence Livermore
Received: 28 Jan 2021 | Accepted: 02 Aug 2021 | Published: 04 Aug 2021
© 2021 Kyosuke Okuda
This is an open access article distributed under the terms of the Creative Commons Attribution License (CC BY 4.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
Citation:
Okuda K (2021) Re-description of the assassin bug species Pygolampis striata Miller, 1940 with new distributional records from Japan and Indonesia (Heteroptera, Reduviidae, Stenopodainae). Biodiversity Data Journal 9: e63695. https://doi.org/10.3897/BDJ.9.e63695
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Pygolampis striata Miller, 1940 was previously described, based on a single male specimen. However, there are no records of the species since then. The females and nymphs were not described and knowledge about their habitat is insufficient.
This is the first record of the assassin bug Pygolampis striata Miller, 1940 from Japan and Indonesia. Here, this species has been re-described and, for the first time, the female has been described. The species was collected from the surfaces of dried Poaceae grasslands using the "Gasa-Gasa collecting method".
Heteroptera, re-description, Reduviidae, Japan, Indonesia, Stenopodainae, Pygolampis striata
The subfamily Stenopodainae (Hemiptera: Heteroptera: Reduviidae) comprises more than 720 species in 115 genera worldwide and is primarily found in the Tropics (
Pygolampis Germar, 1817 is the second largest genus in the subfamily Stenopodainae and contains 92 species worldwide. Ethiopian and Oriental Regions are especially species-rich, with approximately 74 known species (
Dried specimens were used, their morphological characteristics and genital structures were observed and measured under a stereomicroscope (Olympus SZ40, Olympus, Tokyo), equipped with a micrometer. For easier observation, male and female genitalia were soaked in hot 10% potassium hydroxide (KOH) solution for approximately 10 minutes to clear the soft tissues. Photographs of specimens were taken using a single-lens reflex camera (Canon 7D Mark II, Canon, Tokyo), equipped with a Canon macro lens EF 100 mm and MP-E 65 mm. All morphological terminology used herein follows
Depositories of the related specimens are abbreviated as follows:
Pygolampis striata:
Pygolampis sp.:
Male. Colouration. Body generally whitish-brown to pale brown on dorsal side (Fig.
Vestiture. Head densely covered with whitish decumbent pubescence, interantennal tubercle with setae at apex. Eye glabrous. Antennal segment I with decumbent pubescence; segments II–IV with whitish sub-erect setae, as long as the diameter of each segment. Labium with sparse short blackish sub-erect setae, as long as the diameter of half of each segment. Pronotum with densely covered whitish pubescence, three longitudinal rows of whitish pubescence rows on lateral side. Scutellum without pubescence. Hemelytra with whitish pubescence on the corium and veins. Abdomen with fine pubescence. Hind leg tibia with setae subapically; mid- and hind leg tibia with dense setae uniformly.
Structure. Body elongate. Head (Fig.
Pygolampis striata Miller, 1940, a–b: head, a. dorsal view, b. lateral view, c. antennal segment I, d–e: apex of abdomen ventral view, d. male, e. female, f–h: pygophore, f. lateral view omitted on left paramere, g. caudal view, h. dorsal view, i. parameres, j–k: phallus, j. lateral view, k. dorsal view (Lettering: Bp = Basal plate; Pd = pedicel; Plb = phallobase; Plt = phallotheca), l styloides. Setae omitted in a, b, d–k. Scale bar: a–e, 1.0 mm, f–l, 0.5 mm.
Male genitalia. Pygophore (Fig.
Female. General aspect as in male (Fig.
Measurements: [in mm, male (n = 7)/female (n = 9)]. Body length 15.80–16.50/17.50–19.50; head length 2.05–2.25/2.00–2.35; length of anteocular part 0.85–0.90/0.85–1.00; length of postocular part 0.65–0.75/0.65–0.75; lengths of antennal segments I 2.25–2.35/2.40–2.95, II 2.25–2.60/2.30–2.80, III 0.40–0.50/0.40–0.60, IV 0.80–1.30/0.90–1.25; lengths of visible labial segments I 1.35–1.60/1.50–1.75, II 0.45–0.55/0.40–0.50, III 0.35–0.40/0.30–0.40; length of pronotum (including propleural spines) 3.00–3.30/3.10–3.75; maximum width of thorax 1.75–1.95/1.75–2.10; length of scutellum 0.75–1.00/0.80–1.05; maximum width of scutellum 0.50–0.60/0.50–0.75; length of the hemelytron 9.1–10.0/10.0–11.5; length of fore leg femur 3.00–3.20/3.00–3.20, tibia 2.70/2.70, tarsus 0.65–0.70/0.70; of mid-leg femur 3.40–3.50/3.20–4.00, tibia 2.75/2.75–3.20, tarsus 0.75–0.80/0.65–0.80; of hind leg femur 7.50–8.00/7.50–8.00, tibia 7.50–8.00/7.50–8.00, tarsus 0.90–1.00/0.90–1.00.
This species can be distinglished from other species of Pygolampis by the following set of characters: body length 15.80−16.50 mm in the male, 17.50−19.50 mm in female, generally whitish-brown to pale brown, with densely covered whitish decumbent pubescence on dorsal side; pronotum with three longitudinal rows of whitish pubescence on lateral side; abdomen dark brown on ventral side with sparse yellow spots; abdominal segment VII posterior angle shown as Fig.
In general appearance, Pygolampis striata Miller, 1940 is very similar to P. bidentata (Gozze, 1977), but can be distinguished from the latter by a combination of the following characters: generally whitish-brown to pale brown (in P. bidentata, generally dark brown); thorax with three longitudinal rows of whitish pubescence on lateral side (in P. bidentata, thorax without three longitudinal rows); abdomen dark brown on ventral side with sparse yellow spots (in P. bidentata, abdomen without sparse yellow spots ventrally). Additionally, similar distribution to P. foeda Stål, 1859 in Japan, but can be distinguished from the latter by a combination of the following characteristics: pale brown body and thorax with three longitudinal rows of whitish pubescence on lateral side. (in P. foeda, generally reddish-brown-dark brown, thorax without three longitudinal rows of whitish pubescence on lateral side); scape approximately 1.0–1.1 times as long as head length (in P. foeda, scape approximately 1.2–1.4 times as long as head length); posterior angle projecting backwards, weakly concave at middle. (in P. foeda, posterior angle projecting backwards, slightly deep concave at middle).
Japan: Honshu, Kyusyu, Ryukyus [Amami-ôshima Is.], Indonesia [East Kalimantan], Malaysia [Sandakan].
In Honshu, Japan, there is no specimen of the collection since 1981, indicating the likelihood that the species might be extinct in the region.
Some studies have evaluated heteropteran fauna in Amami-ôshima (
Therefore, the collection of specimens of this species using methods other than light traps is difficult. Even with light traps, it is difficult to target and collect certain species; P. striata and many Stenopodainae members require a special collection method.
I acknowledge Akihiro Yoshikawa (Amami, Kagoshima Japan) and Takahiro Komatsu (Miyazaki, Miyazaki Japan) for kindly providing the specimens used in this study. I greatly appreciate Tadashi Ishikawa (Tokyo University of Agriculture, Atsugi, Japan), Yukinobu Nakatani (National Institute for Agro-Environmental Sciences, Tsukuba, Japan), Akiko Saito and Teruaki Ban (Natural History Museum and Institute, Chiba, Japan) for loaning the material used in this study. I am grateful to Jun Souma (Kyusyu University, Fukuoka, Japan) for his assistance in submitting this manuscript. I am very grateful to Laurence Livermore (The National History Museum, London, UK), Hélcio R. Gil-Santana (Instituto Oswaldo Cruz, Rio de Janeiro, RJ, Brazil) and Liu Yingqi (China Agricultural University, Beijing, China) for their critical comments and suggestions on this manuscript. I would like to thank Editage (www.editage.com) for English language editing.