Simulium (Boreosimulium) konoi ( Takahasi, 1950 )
publication ID |
https://doi.org/ 10.12651/JSR.2020.9.1.019 |
DOI |
https://doi.org/10.5281/zenodo.8140360 |
persistent identifier |
https://treatment.plazi.org/id/03D48785-3006-4623-FF78-DD39D83E9C8C |
treatment provided by |
Felipe |
scientific name |
Simulium (Boreosimulium) konoi ( Takahasi, 1950 ) |
status |
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Simulium (Boreosimulium) konoi ( Takahasi, 1950) View in CoL View at ENA
( Figs. 1-4 View Fig View Fig View Fig View Fig )
Nevermannia konoi Takahasi, 1950: 1556 View in CoL . Type locality: Tottori, Honshu , Japan.
Simulium (Nevermannia) yamayaense Ogata & Sasa, 1954: 326-327 View in CoL . Type locality: Honshu, Japan; Takaoka & Okazawa, 1988: 99 (Japanese list); Uemoto, 1991: 191 (synonymization).
Simulium (Nevermannia) liaodongense Sun, 2012: 46- 49 . Type locality: Liaoning, China; Adler & Crosskey, 2014 (synonymization).
Simulium sp. J-9 Bentinck, 1955: 6; Takahasi, 1971 (synonymization).
Simulium (Eusimulium) sp. View in CoL Ogata & Sasa, 1955: 14 (Japanese key).
Simulium (Boreosimulium) konoi: Sato et al., 2004 View in CoL (taxonomy, redescription); Adler, 2019 (world list).
Simulium (Nevermannia) konoi: Ogata & Sasa, 1954: 328 View in CoL (Japanese list and key); Ogata & Sasa, 1955: 11 (Japanese list and key); Shogaki, 1956: 275 (Japanese list); Ogata et al., 1956: 76-77 (description); Takahasi, 1971: 80 (taxonomic notes); Takaoka & Okazawa, 1988: 98 (Japanese list).
Eusimulium konoi: Orii et al., 1969: 3 View in CoL (Japanese key); Uemoto, 1991: 191 (taxonomic note); Uemoto, 2005: 1017 (Japanese key, illustration).
Simulium (Eusimulium) konoi: Ogata & Uemoto, 1971: 80 View in CoL (illustration); Matsuo & Uemoto, 1975: 130-133 (morphology).
Simulium (Gomphostilbia) konoi: Uemoto, 1985: 330 View in CoL (Japanese key).
Simulium (Eusimulium) yamayaense: Ogata et al., 1956: 74 View in CoL (morphology); Shogaki & Shimizu, 1956: 373 (illustration); Okamoto, 1958: 583 (taxonomic notes, illustration); Ogata & Uemoto, 1971: 77 (illustration); Uemoto, 1985: 330 (Japanese key).
Eusimulium yamayaense: Orii et al., 1969: 9-11 (Japanese key).
Cnetha konoi: Yankovsky, 2001: 305 (Russian key).
Cnetha konoi: Ono, 1979 (misidentification of Simulium oligotuberculatum ( Knoz, 1965)) View in CoL .
Diagnosis. This species can be distinguished from other black flies by the following combination of characteristics: female cibarium equipped with oblique rows of denticles; male ventral plate well-developed W or inverted Vshaped; pupa with 4 gill filaments; larva with thorax and abdomen densely covered with short branched dark setae; larval antenna with 3 hyaline bands.
Description. Female ( Fig. 1 View Fig ). Body length ( Fig. 1A View Fig ): 2.6- 2.8 mm (n = 10). Head ( Fig. 1B View Fig ). As wide as thorax. Eye dichoptic. Antenna 11 segmented, terminal segment with 3-4 apical setae. Frons dark brown to black, dull densely covered with whitish golden hairs. Clypeus dorsally and laterally with dark brown, medially brown with whitish hairs, pruinosity. Maxillary palp ( Fig. 1C View Fig ) 5 segmented, proportional ratio of 3 rd to 5 th segments 1: 1.2-1.3: 2.4- 2.6; sensory vesicle 0.4 × as long as 3 rd segment. Mandible with ca. 25 serrations. Maxillary lacinia ( Fig. 1C View Fig ) with 23-27 teeth. Cibarium ( Fig. 1D, E View Fig ) with ca. 70-80 water drop-shaped oblique rows of denticles anteriorly. Hypopharynx with 20-30 spine-like serrations. Thorax ( Fig. 1F View Fig ). Wing length: 2.5-2.7 mm. Basal section of radius with dorsal hairs. Scutum dark brown to black with densely covered with whitish golden hairs. Scutellum light brown with long golden hairs, apically with long black hairs. Pleural membrane light brown, bare. Katepisternum brown, bare. Legs. All femora and tibiae brownish yellow with apex brown. Tarsi dark brown. Hind leg with basitarsus ( Fig. 1G View Fig ) with calcipala distinct, 1.6× as long as tarsomere 1-4 combined. Pedisulcus distinct. Tarsal claw with well-developed thumblike lobe, 0.64 × as long as claw. Abdomen. Brown to dark brown, moderately covered with whitish hairs except abdominal segments 3-7 with dark long hairs near each spiracles. Genitalia ( Fig. 1H View Fig ). Genital fork with space between each arms semi-round. Anal lobe moderately produced ventrally, rounded, 13-17 long hairs. Cercus small, rounded posteriorly, setose. Spermatheca ( Fig. 1I View Fig ) slightly longer than wide, with distinct reticulate pattern.
Male ( Fig. 2 View Fig ). Body length ( Fig. 2A View Fig ): 2.4-2.7 mm (n = 10). Head ( Fig. 2B View Fig ). Wider than thorax. Eye holoptic. Upper corneal facets consisting of 15-17 vertical rows and 20- 22 horizontal rows. Antenna ( Fig. 2C View Fig ) 11 segmented, terminal segment with 3-5 apical setae. Clypeus dark brown, pruinosity, moderately covered with yellowish hairs. Maxillary palp ( Fig. 2D View Fig ) 5 segmented, proportional ratio of 3 rd to 5 th segments 1: 1.1-1.3: 2.4-2.6; sensory vesicle 0.2 × as long as 3 rd segment. Maxillary lacinia with 15-18 short setae, not well serrated. Cibarium ( Fig. 2E View Fig ) without denticles. Hypopharynx with 15-20 apical setae. Thorax ( Fig. 2F View Fig ). Wing length: 2.2-2.5 mm. Basal section of radius with dorsal hairs. Scutum brownish black, densely covered with golden hairs, posteriorly with long reclinate hairs. Scutellum yellowish brown with long black hairs and sparse golden hairs. Pleural membrane brown, bare. Katepisternum brown, bare. Legs. All femora and tibiae yellowish brown with apex brown. Tarsi brown to dark brown. Hind leg with basitarsus ( Fig. 2G View Fig ) with calcipala distinct, 1.4 × as long as tarsomere 1-4 combined. Pedisulcus distinct. Tarsal claw small without thumb-like lobe. Abdomen brown to dark brown with all hairs brown to dark brown. Genitalia ( Fig. 2H, I View Fig ). Gonostylus slender, tapered to pointed apex, gently curved inwardly, with single small spinule. Ventral plate with well developed median keel, W or inverted Vshaped in ventral view. Median sclerite elongate, thin. Cercus small, rounded. Paramere moderate sized, 8-11 hooks, each with 10- 15 short setae.
Pupa ( Fig. 3 View Fig ). Body length ( Fig. 3A, B View Fig ): 2.7-3.0 mm (n = 10). Body ( Fig. 3B, C View Fig ) brown to reddishbrown ground color. Gill ( Fig. 4B View Fig ) with 4 filaments, equal in size, 0.8 × as long as pupal body length (2.2-2.5 mm), angle between uppermost and lowermost filaments less than 90°. Cephalic plate and vertex ( Fig. 3D View Fig ) bare, without tubercles. Frons with 3 pairs of short trichomes, simple, less than half the length of facial trichome, only visible in high magnification; face with 1 medium long trichome, simple, about half the length of thoracic trichomes. Thorax ( Fig. 3D View Fig ) bare anteriorly, moderately covered with small tubercles posteriorly; thoracic trichome ( Fig. 3E View Fig ) in 6 pairs, simple (unbranched), long. Abdomen ( Fig. 3C View Fig ). Abdominal tergites III and IV with 4 anteriorly directed spin hooks on posterior margin. Tergites V- IX with spine combs, spines on tergite V smallest, tergite VIII largest. Terminal hooks well developed. Cocoon ( Fig. 3A View Fig ) slipper-shaped, tightly woven, as long as pupa.
Larva ( Fig. 4 View Fig ). Body length ( Fig. 4A, B View Fig ): 5.3-5.7 mm (n = 10). Body ( Fig. 4A, B View Fig ) reddishbrown or brownishgrey ground color. Gill histoblast ( Fig. 4A, B View Fig ) 4 filaments. Head ( Fig. 4C View Fig ) with head spots positive; anteromedial spots 4, separated, distinct; first and second anterolateral spots obliquely elongated, separated, parallel with each other; posteromedial spots narrow, distinct, 1.3× as long as anteromedial spots; first and second posterolateral spots separated, distinct. Single spot under ocellus. Antenna ( Fig. 4D View Fig ) brown with 3 hyaline bands, 1.2 × as long as labral fan stem, proportional ratio of antennal segments 1: 1.4: 0.8. Labral fan with 35-38 primary rays. Postgenal cleft ( Fig. 4E View Fig ) not clearly defined, round, as long as wide, laterally with elongate spot. Hypostoma ( Fig. 4F View Fig ) with 9 teeth, lateral and median teeth subequal in length, basally with 3-4 hypostomal setae. Subesophageal ganglion darkly pigmented. Thorax and abdomen densely covered with short branched black setae dorsally and laterally ( Fig. 4G, H View Fig ). Rectal papillae ( Fig. 4H, I View Fig ) of 3 compound lobe with 6-7 secondary lobules. Ventral tubercle absent ( Fig. 4I View Fig ). Posterior proleg ( Fig. 4J View Fig ) with 10-12 hooks (posterior circlet), 60-65 rows.
Specimens examined. Korea: Gyeonggi-do, Gapyeonggun, Buk-myeon, Jeokmok-ri , Gapyeongcheon stream, 37°57 ʹ 48 ʺ N, 127°26 ʹ 58 ʺ E, altitude 290 m. 10.v.2019, SK Kim (159 ultimate, 187 penultimate, 72 early instar larvae, 50 pupae (except for rearing), GoogleMaps 16♂, 32$; Gyeonggido, Gapyeonggun, Bukmyeon, Dodaeri, Myeongjicheon stream, 37°56 ʹ 07 ʺ N, 127°29 ʹ 18 ʺ E, altitude 210 m, 22.v.2019, SK Kim (1 ultimate, 6 penultimate instar larvae). GoogleMaps
Distribution. Korea (Gyeonggi-do, new record), China (Liaoning), Japan (Hokkaido, Honshu, Kyushu, Shikoku), Siberia (Far East).
Stream information. Two streams, the only localities where larvae and pupae of S. konoi were collected so far, were separated by Mt. Myeongjisan (1,267 m) by a distance of 4.6 km. Both streams were medium to large-sized streams with moderate to rapid flow and stream beds consisting of boulders and rubble, and totally exposed to the sun. Edges of the streams were lined with trailing vegetations including reeds. The streams were 10-20 m wide and 15-20 cm deep, but the streams were partially dried up due to spring drought.
Biological notes. Larvae were collected from trailing vegetation, submerged twigs, and dead leaves. Body colors of fresh larvae were brownish red or brownish grey when fully matured. Specimens were collected along with Prosimulium kiotoense , Simulium japonicum , Simulium malyschevi , Simulium suzukii , and Simulium yamatoense (the latter was previously misidentified as S. rufibasis ). All larvae and pupae were collected only twice in May 2019 from two streams, and I failed to collect S. konoi in subsequent attempts in other months at the same streams, suggesting S. konoi is univoltine as Sato et al. (2004) suggested. In Japan as well, larvae and pupae of S. konoi were collected only in April and had not been found in other months ( Sato et al., 2004).
Remarks. Subgenus Boreosimulium contains three species-groups: annulus species-group where S. konoi belongs to, baffinense species-group, and johannseni species-group ( Adler, 2019). The most distinctive characteristic of S. konoi is several rows of denticles on the female cibarium as Bentinck (1955) and Sato et al. (2004) recognized. Placement of S. konoi in the subgenus Boreosimulium is somewhat problematic since S. konoi possess many characteristics that do not match the diagnosis for Boreosimulium , such as denticles on the cibarium of the female, the bi-colored legs of the female, and short black setae on the larval abdomen. Cibarial armature are present in species of Psilopelmia , Psilozia and Hemicnetha ( Adler et al., 2004) , but the shape and position of armature is different in S. konoi . Furthermore, chromosomal analysis showed that the chromosomes of S. konoi were very different and it did not match the typical chromosomes of Boreosimulium (e.g., annulus species-group) (Peter H. Adler, pers. comm.). Features of Korean S. konoi specimens matched those of Japanese specimens in almost all details, with some degree of geographical variation, such as ventral tubercle on larval abdominal segment IX and shape of larval head spots. Due to the autapomorphy and other characters found in S. konoi , the current placement of S. konoi in the subgenus Boreosimulium or species-group assignment is tentative, and future research is warranted to clarify the placement of the S. konoi in the subgenus or species-group.
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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Boreosimulium |
Simulium (Boreosimulium) konoi ( Takahasi, 1950 )
Kim, Sam-Kyu 2020 |
Simulium (Nevermannia) liaodongense
Sun, Y. X. 2012: 49 |
Cnetha konoi:
Yankovsky, A. V. 2001: 305 |
Simulium (Gomphostilbia) konoi: Uemoto, 1985: 330
Uemoto, K. 1985: 330 |
Simulium (Eusimulium) konoi:
Matsuo, K. & K. Uemoto 1975: 130 |
Ogata, K. & K. Uemoto 1971: 80 |
Eusimulium konoi:
Uemoto, K. 2005: 1017 |
Orii, T. & K. Uemoto & O. Onishi 1969: 3 |
Eusimulium yamayaense:
Orii, T. & K. Uemoto & O. Onishi 1969: 11 |
Simulium (Eusimulium) yamayaense:
Ogata, K. & K. Uemoto 1971: 77 |
Okamoto, M. 1958: 583 |
Ogata, K. & M. Sasa & T. Suzuki 1956: 74 |
Shogaki, Y. & T. Shimizu 1956: 373 |
Simulium sp.
Bentinck, W. 1955: 6 |
Simulium (Eusimulium) sp.
Ogata, K. & M. Sasa 1955: 14 |
Simulium (Nevermannia) yamayaense
Uemoto, K. 1991: 191 |
Takaoka, H. & T. Okazawa 1988: 99 |
Ogata, K. & M. Sasa 1954: 327 |
Simulium (Nevermannia) konoi:
Takaoka, H. & T. Okazawa 1988: 98 |
Takahasi, H. 1971: 80 |
Ogata, K. & M. Sasa & T. Suzuki 1956: 76 |
Ogata, K. & M. Sasa 1955: 11 |
Ogata, K. & M. Sasa 1954: 328 |
Nevermannia konoi
Takahasi, H. 1950: 1556 |