Ostrovus kyushuensis, Hanada, 2025

Hanada, Satoko, 2025, A new species of the genus Ostrovus Ricker, 1952 (Plecoptera: Perlodidae) from northern Kyushu, Japan, with notes on the male drumming signal, Zootaxa 5653 (3), pp. 324-342 : 326-339

publication ID

https://doi.org/10.11646/zootaxa.5653.3.2

publication LSID

lsid:zoobank.org:pub:E772D1FE-38D7-427F-ABEA-C5FE862FCFF1

persistent identifier

https://treatment.plazi.org/id/6778FD75-FF94-0E5B-ADA8-5931FEEFDE47

treatment provided by

Plazi

scientific name

Ostrovus kyushuensis
status

sp. nov.

Ostrovus kyushuensis sp. nov.

( Figs. 1–21 View FIGURES 1–3 View FIGURES 4–9 View FIGURES 10–13 View FIGURES 14–17 View FIGURE 18 View FIGURE 19 View FIGURE 20 View FIGURE 21 )

Ostrovus sp. : Hanada 2014: 18–19; Hanada 2016: 17. Type series. Holotype male: Magaribuchi, Sawara Ward, Fukuoka City, Fukuoka Prefecture, Japan, 33.495356, 130.296219, alt. 232 m, 4.V.2013. Paratypes: 1 male, the type locality, 13.IV.2013; 1 male, the type locality, 19.IV.2014; 1 female with eggs, the type locality, 29.IV.2017; 1 female, the type locality, 24.IV.2019; 1 male, 1 female with eggs, collected by light traps, Kasuga Valley , Yoshida , Ureshino Town, Ureshino City, Saga Prefecture, Japan, 33.023222, 130.034528, alt. 442 m, 25. V.2000 GoogleMaps .

Other specimens examined. The type locality: 1 female, 13.IV.2013; 1 male, 19.IV.2014; 1 male, 1 female, 26.IV.2014; 1 male (a mature nymph collected on 21.IV.2015 and emerged on 22.IV.2015); 1 male, 3. Ⅴ.2015; 1 female, 28.IV.2019. Hoshino Village , Yame City, Fukuoka Prefecture, Japan, 33.216944, 130.809167, alt. 396 m GoogleMaps : 1 female, 1.IV.2021; 1 female, 1.IV.2022. Fujiwara , Mitsuse Village, Saga City, Saga Prefecture, Japan, 33.441719, 130.309589, alt. 480 m GoogleMaps : 1 female, 20. V.2017. Ikisa , Ouchi Town, Karatsu City, Sage Prefecture, Japan, 33.369611, 130.048722, alt. 314 m GoogleMaps : 1 male, 22.IV.2018; 1 male, 18.IV.2021; 1 male, 1. V.2021. Yamase , Hamatama Town, Karatsu City, Saga Prefecture, Japan, 33.372358, 130.055717, alt. 410 m GoogleMaps : 1 male, 29.IV.2018; 1 female, 23. V.2021. Kasuga Valley , Yoshida , Ureshino Town, Ureshino City, Saga Prefecture, Japan, 33.023222, 130.034528, alt. 442 m GoogleMaps : 1 male, 3 females (one female with eggs), collected by light traps, 25. V.2000; 1 female, collected by light traps, 2.VII.2000.

Adult habitus. Wings macropterous in both sexes; male body length 10.1–12.8 mm (mean ± SD = 11.6 ± 0.9, n = 10), female body length 10.5–15.5 mm (mean ± SD = 13.4 ± 1.5, n = 12); male forewing length 12.0–14.0 mm (mean ± SD = 13.2 ± 0.6, n = 10), female forewing length 13.0–15.0 mm (mean ± SD = 14.0 ± 0.6, n = 13).

Head dark brown ( Fig. 1 View FIGURES 1–3 ), or dark brown with pale brown areas near the ocelli and on the occiput; the pale brown areas variable in shade and extent, frequently indistinct; obscure darker markings at the back of each posterior ocellus ( Fig. 2 View FIGURES 1–3 , arrows); M line indistinct ( Fig. 2 View FIGURES 1–3 ). Compound eyes and three ocelli black. Antenna dark brown; scape darker than the rest of the segments. Ventral surface of the head is dark brown. Labial palpus and maxillary palpus are brown.

Pronotum rectangle with rounded anterolateral angles and slightly curved anterior edge, wider than long, bearing an elliptic groove along the edge, dark brown with a pale brown or yellow-brown median band, or uniformly dark brown; near anterior and posterior margins of the groove darker in color; worm marks few and indistinct ( Figs. 1 & 2 View FIGURES 1–3 ). Meso- and metanotum dark brown, sometimes with a pale-colored median narrow line on mesonotum and a pale-colored spot on metanotum. Mesosternum is typical for the genus presented by Ricker (1952).

Wings blackish except the whitish yellow costal region ( Fig. 1 View FIGURES 1–3 ). Longitudinal veins C and Sc and crossveins between C and Sc whitish yellow; other veins dark brown. Wing venation shown in Fig. 3 View FIGURES 1–3 : 2–7 crossveins (3–7 in forewing, 2–5 in hindwing) between C and Sc besides humeral cross-vein (h); 1–4 crossveins (2–4 in forewing, 1–4 in hindwing) between C and R 1; RS branches 2 or 3 times.

Coxae and trochanters pale yellow. In fore and mid legs, femora and tibiae brown to dark brown except the pale yellowish basal two-fifths (range: 1/5–3/5) of femora, however, tibia of mid leg rarely with a pale yellowish area on the distal half; femur and tibia of hind leg pale yellow except the brownish distal two-fifths (range: 3/10–7/10) of femur and except the brownish basal three-tenths (range: 1/10–1/2) of tibia, however, tibia of hind leg rarely without the pale yellowish area. Tarsi and claws brown. Cercus dark brown, 9–12 segmented; length of cercus 3–4 mm.

Male. Abdominal terga 1–7 unmodified, mostly brown with slightly darker areas on either side and the middle except terga 1–3 or 1–2 with a pair of small, whitish, weakly sclerotized areas. Tergum 8 with a long, truncated projection well over the anterior border of tergum 9 ( Figs. 4 & 5 View FIGURES 4–9 ); the projection apex with shallow emarginate tip ( Fig. 5 View FIGURES 4–9 ). Anterior margin of tergum 9 with a weakly sclerotized semi-elliptical area, occupying about one-third of the width of tergum 9 ( Figs. 5 & 6 View FIGURES 4–9 ). Tergum 10 incompletely divided; the both sides of the cleft forming hemitergal lobes ( Fig. 5 View FIGURES 4–9 ). Paragenital plate short ( Fig. 5 View FIGURES 4–9 ). Paraproct expanded and protruded dorsally, looking like bearing a small concave at the base in lateral view ( Figs. 5 & 7 View FIGURES 4–9 , arrow). Terga 8–10 and paragenital plates and paraprocts dark brown except the basal area of the projection of tergum 8 and the weakly sclerotized area of tergum 9, being whitish. Abdominal sterna 1–6 unmodified and dark brown. Sterna 7 with a small ventral lobe, produced caudally ( Fig. 8 View FIGURES 4–9 , vl). Ventral lobe on sternum 8 absent ( Fig. 8 View FIGURES 4–9 ) or slightly suggested. Sternum 9 long, covering the anterior part of sternum 10; its posterior margin parabolic ( Fig. 8 View FIGURES 4–9 ). Sterna 7–10 dark brown except the central whitish area of sternum 10. Aedeagus short and completely membranous; everted aedeagus with a pair of small ventral lobes near the base and with two bulges at the top ( Fig. 9 View FIGURES 4–9 ). Epiproct composed of an epiproct tip, a lever arm, a basal anchor and a lateral arm, and lateral stylets absent ( Figs. 10–13 View FIGURES 10–13 ): epiproct tip composed of a large and well sclerotized frame-shaped median support with a semicircular dorsal top and a beak-shaped apex in lateral view ( Figs. 4 View FIGURES 4–9 & 10 View FIGURES 10–13 middle & 11) and with a lateral membranous expansion on the either side on the median support ( Figs. 10 View FIGURES 10–13 upper, lower & 11); lever arm stout and strongly curved ( Fig. 11 View FIGURES 10–13 ); basal anchor somewhat rounded and transparent except the brown basal area connected the lateral arms ( Figs. 12 & 13 View FIGURES 10–13 ); lateral arm large and bilobed ( Figs. 11 & 13 View FIGURES 10–13 ).

Female. Abdominal terga brownish except terga 1–3 or 1–2 bearing a pair of whitish, small, weakly sclerotized areas. Abdominal segment 8 swollen on both posterolateral sides ( Fig. 14 View FIGURES 14–17 ). Abdominal sterna pale yellow; subgenital plate pale yellowish brown and sometimes partly brownish; the dorsal of subgenital plate having a small whitish semicircular area, near the vulva ( Fig. 15 View FIGURES 14–17 , arrow with an asterisk). Subgenital plate large, and slightly longer than sternum 9, with a shallow midline concave ( Figs. 14 & 16 View FIGURES 14–17 ). A pair of pale yellowish brown sclerites located on sternum 9, near the vulva ( Fig. 16 View FIGURES 14–17 , arrows).

Egg. Pale yellow, turtleback-shaped with a rounded fingernail-like collar ( Fig. 17 View FIGURES 14–17 ). Anchor located the ventral side of the collar ( Fig. 17 View FIGURES 14–17 lower). The egg is morphologically indistinguishable from that of O. mitsukonis (see Isobe 1997: figs. 11A–C).

Drumming signals. Two of the three observed males displayed drumming behavior. One reared 11-day old and one captured 6-day old male produced calls by tapping the ventral lobe upon the recording chamber substrate (see Figs. 4 & 8 View FIGURES 4–9 , vl). The male call patterns were composed of alternate short and long beat intervals ( Fig. 18 View FIGURE 18 ). Since the short beat intervals had consistent inter-beat intervals with a 9.9 ms mean interval difference calculated by subtracting minimum mean interval from maximum mean interval (95.1 ms of G3–85.2 ms of G1 = 9.9 ms≤10 ms) ( Fig. 19 View FIGURE 19 ), they were considered intra-group intervals. Thus, the male call of the new species was described as a grouped bi-beat call signal pattern.

Most of the beat groups consisted of 2 beats and had 90.2 ± 7.3 ms intra-group intervals ( Fig. 19 View FIGURE 19 , Table 1). However, beat groups 1 and 2 were sometimes aberrant, consisting of only one beat (45% and 10%, respectively). The male call signals were composed of 9–15 groups per signal (mean ± SD = 11.8 ± 1.7) with somewhat consistent 140.6 ± 22.7 ms inter-group intervals ( Figs. 18 View FIGURE 18 & 20 View FIGURE 20 , Table 1).

The amplitudes of beats were low at the beginning of the signal (around the beat groups 1–5) and then gradually increasing ( Fig. 18 View FIGURE 18 ). The inter-group interval showed a tendency to be unstable at the beginning of the signal (igi1–igi2) and then to be slightly longer with signal progress ( Fig. 20 View FIGURE 20 ). The mean interval difference of inter-group interval was 63.7 ms (194.5 ms of igi14–130.8 ms of igi3 = 63.7 ms) ( Fig. 20 View FIGURE 20 ). Total signal duration and total number of beats per signal averaged 2533.0 ± 505.9 ms (range: 2017.3–3639.7, n = 20) and 23.1 ± 3.6 beats (range: 16–29, n = 20), respectively.

Ecological notes. The new species inhabits the upper reaches of rivers ( Fig. 21 View FIGURE 21 ). Adults were found in spring and early summer (April–July).

Distribution. Japan (northern Kyushu).

Etymology. The species name refers to Kyushu, one of the Japanese main islands from which the holotype was collected. Japanese common name: Nishi-kogusa-himekawagera.

Remarks. The characteristics of the new species and two known species of the genus Ostrovus , O. mitsukonis and O. nikkoensis are summarized in Table 2 and Table 3. As for O. nikkoensis three females from Nasushiobara City, Tochigi Prefecture, near the type locality of O. nikkoensis , were compared with the digital images of the type and agreed with the type in the following characteristics (see Table 2): the color pattern of the head in dorsal and ventral (see Figs. 23 & 25 View FIGURES 22–25 ); the pronotum with a yellowish brown band (see Fig. 23 View FIGURES 22–25 ); the colors of the scape and the pedicel (see Figs.24 & 25 View FIGURES 22–25 ); the large subgenital plate with a median shallow concavity (see Fig. 44 View FIGURES 43–44 ); the forewing length (the type: 14.5 mm, the three females: 14.0 mm, 14.8 mm, 15.3 mm). Therefore, I identified the three females as O. nikkoensis . Additionally, ten males collected with the three females likely also represent O. nikkoensis , their morphological characteristics being shown in Table 2 and 3 and depicted in illustrations based on these males.

Male epiproct of each species in Ostrovus shows species-specific characteristics ( Table 2, Figs. 10 View FIGURES 10–13 , 34 View FIGURES 34 & 42 View FIGURES 42 ), and moreover, the shape of the weakly sclerotized area at male abdominal tergum 9 ( Figs. 5, 6 View FIGURES 4–9 , 28 View FIGURES 26–29 & 40 View FIGURES 37–41 ) and the shape of the male paraproct ( Figs. 7 View FIGURES 4–9 , 29 View FIGURES 26–29 & 41 View FIGURES 37–41 ) are also probably species-specific. In contrast, the characteristics of the projection on male abdominal tergum 9 ( Figs. 5 View FIGURES 4–9 , 27 View FIGURES 26–29 & 38 View FIGURES 37–41 ), especially the shape of the tip and the width, could be varied even among individuals of the same species ( Figs. 27 View FIGURES 26–29 , 30–33 View FIGURES 30–33 , 38 & 39 View FIGURES 37–41 ).

Females of the three species have similar large subgenital plates ( Figs. 16 View FIGURES 14–17 , 36 View FIGURES 35–36 & 44 View FIGURES 43–44 ). Therefore, examinations must include multiple characteristics to distinguish the species: color patterns of the head and antenna (especially the pedicel) and the pronotum ( Table 2). However, the color on the dorsal surface of the head in both sexes is somewhat variable, and sometimes the light-colored areas are darker and thus indistinct. Forewing length and the index of distance between compound eyes / width of a compound eye in dorsal view could be helpful to distinguish O. mitsukonis from the other two species ( Table 3).

Ricker (1952) described the probable male of O. nikkoensis based on a single male specimen from Ogawa, in the southern part of Shinano Province (the present Nagano Prefecture or Gifu Prefecture), Honshu, Japan. By Ricker’s illustration, the male has a weakly sclerotized area at abdominal tergum 9, whose shape is a transversally narrow band approximately 2/3 as wide as tergum 9 (see Ricker 1952, fig. 75). The characteristic disagrees with those of the three species of Ostrovus (see Table 2), and therefore the male is probably an undescribed species of Ostrovus .

V

Royal British Columbia Museum - Herbarium

Royal British Columbia Museum - Herbarium

R

Departamento de Geologia, Universidad de Chile

Kingdom

Animalia

Phylum

Arthropoda

Class

Insecta

Order

Plecoptera

Family

Perlodidae

Genus

Ostrovus

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