Research Article |
Corresponding author: Hyojoong Kim ( hkim@kunsan.ac.kr ) Academic editor: Mostafa Ghafouri Moghaddam
© 2024 Ju-Hyeong Sohn, Cornelis van Achterberg, Sangjin Kim, Hyojoong Kim.
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:
Sohn J-H, van Achterberg C, Kim S, Kim H (2024) Five new species and one new record of the genus Phaenocarpa Foerster (Hymenoptera, Braconidae, Alysiinae) from South Korea. ZooKeys 1217: 173-193. https://doi.org/10.3897/zookeys.1217.129916
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Five new species of the genus Phaenocarpa Foester, 1863 (Braconidae: Alysiinae) are described and illustrated: P. acutidentata Sohn & van Achterberg, sp. nov., P. tacitoides Sohn & van Achterberg, sp. nov., P. setosa Sohn & van Achterberg, sp. nov., P. tanycauda Sohn & van Achterberg, sp. nov., and P. angusticeps Sohn & van Achterberg, sp. nov. Additionally, P. tacita Stelfox, 1941 is recorded for the first time from South Korea. The barcode region of mitochondrial cytochrome c oxidase I (COI) was also analyzed for the seven congeneric species including one from GenBank. In addition, an identification key for the Phaenocarpa species recorded in Korea is provided.
Alysiini, Hymenoptera, new species, parasitoid wasp, phylogeny, taxonomy
The subfamily Alysiinae is a relatively large taxon in the family Braconidae, consisting of more than 2,440 valid species worldwide (
The genus Phaenocarpa Foerster, 1863 is a large and worldwide genus of Alysiinae, which includes 231 species in nine subgenera (
In Korea,
In this study, we used the cytochrome c oxidase I (COI), barcode region of the Korean seven Phaenocarpa species to confirm their pairwise genetic distances. The comparative diagnoses provides the diagnosis of each new and unrecorded species, comparing them with species that have similar characters. Descriptions, diagnoses, identification keys, and photographs of the diagnostic characters are also provided.
Samples of the new species were collected using Malaise traps in South Korea at Mt. Odaesan (Gangwon-do), Mt. Kalbong (Gyeonggi-do), and Gwaneumsa Temple (Jeju-do). The sorting and preparation were performed at the
Animal Systematics Laboratory (ASL),
Department of Biological Science, Kunsan National University (
For DNA analyses, whole genomic DNA was extracted from the specimens using a Labopass Tissue kit (Cosmo Genetech, Daejeon, Korea) following the manufacturer’s protocol. In order to conserve morphologically complete voucher specimens, the ‘non-destructive method’ by
A total of 586 bp of the COI fragments were sequenced from P. tacita Stelfox, P. acutidentata sp. nov., P. tacitoides sp. nov., P. setosa sp. nov., P. tanycauda sp. nov., and P. angusticeps sp. nov. that were deposited in GenBank (accession numbers PP587250–PP587256) (Table
No | Species | NCBI accession number | Reference |
---|---|---|---|
1 | P. acutidentata Sohn & van Achterberg, sp. nov. | PP587250 | this study |
2 | P. angusticeps Sohn & van Achterberg, sp. nov. | PP587255 | this study |
3 | P. artotemporalis Sohn & van Achterberg, 2021 | MZ318086 |
|
4 | P. brachyura Sohn & van Achterberg, 2021 | MZ318087 |
|
5 | P. fidelis Fischer, 1970 | MZ318083 |
|
6 | P. lobata Sohn & van Achterberg, 2021 | MZ318085 |
|
7 | P. masha Sohn & van Achterberg, 2021 | MW376066 |
|
8 | P. ruficeps (Nees, 1812) | MZ318084 |
|
9 | P. setosa Sohn & van Achterberg, sp. nov. | PP587252 | this study |
10 | P. tacita Stelfox, 1941 | PP587256 | this study |
11 | P. tacitoides Sohn & van Achterberg, sp. nov. | PP587251 | this study |
12 | P. tanycauda Sohn & van Achterberg, sp. nov. | PP587254 | this study |
Calculated genetics distance, based on COI sequences between Phaenocarpa species used in the analysis.
P. acutidentata | P. angusticeps | P. artotemporalis | P. brachyura | P. fidelis | P. lobata | P. masha | P. ruficeps | P. setosa | P. tacita | P. tacitoides | P. tanycauda | |
---|---|---|---|---|---|---|---|---|---|---|---|---|
P. acutidentata | ||||||||||||
P. angusticeps | 0.111 | |||||||||||
P. artotemporalis | 0.162 | 0.140 | ||||||||||
P. brachyura | 0.106 | 0.108 | 0.123 | |||||||||
P. fidelis | 0.104 | 0.108 | 0.125 | 0.072 | ||||||||
P. lobata | 0.097 | 0.104 | 0.128 | 0.072 | 0.053 | |||||||
P. masha | 0.135 | 0.135 | 0.152 | 0.137 | 0.123 | 0.126 | ||||||
P. ruficeps | 0.114 | 0.099 | 0.140 | 0.108 | 0.097 | 0.087 | 0.121 | |||||
P. setosa | 0.099 | 0.114 | 0.147 | 0.094 | 0.094 | 0.094 | 0.125 | 0.101 | ||||
P. tacita | 0.119 | 0.113 | 0.109 | 0.118 | 0.106 | 0.108 | 0.121 | 0.104 | 0.108 | |||
P. tacitoides | 0.104 | 0.104 | 0.133 | 0.096 | 0.096 | 0.108 | 0.126 | 0.097 | 0.099 | 0.108 | ||
P. tanycauda | 0.241 | 0.249 | 0.268 | 0.234 | 0.237 | 0.234 | 0.242 | 0.247 | 0.229 | 0.241 | 0.251 |
Phaenocarpa Foerster, 1863: 267. Type species (by original designation): Alysia picinervis Haliday, 1838.
Third antennal segment shorter than fourth segment; fore wing vein 2–SR shorter than vein 3–SR, vein CU1b longer than vein 3–CU1; vein 1-M of hind wing comparatively long.
Koinobiont endoparasitoids of larvae of Dipteran species (
Cosmopolitan.
1 | Temples distinctly striate ventrally; mesopleuron largely coarsely sculptured; face laterally extensively and finely striate | P. angustiptera Papp, 1968 |
– | Temples smooth ventrally; mesopleuron largely smooth, except for area of precoxal sulcus; face laterally smooth or nearly so | 2 |
2 | Vein r-m of fore wing bordered with blackish setae, resulting in one infuscated patch; mesoscutum with metallic sheen | P. picinervis (Haliday, 1838) |
– | Vein r-m of fore wing normal, not bordered with blackish setae; mesoscutum without metallic sheen | 3 |
3 | Mandible slender, ~ 2.3 × longer than wide; vein 2-1A of fore wing of ♂ strongly widened | P. eunice (Haliday, 1838) |
– | Mandible robust, at most 1.9 × longer than wide; vein 2-1A of fore wing of ♂ narrow | 4 |
4 | Scutellar sulcus evenly narrowed medially, 3–5 × wider than its median length; head more or less reddish or yellowish brown | P. ruficeps (Nees, 1812) |
– | Scutellar sulcus wide medially, 2–3 × wider than long medially; head dark brown or black | 5 |
5 | First tooth of mandible gradually connected to second tooth, forming a straight or arcuate connection (Figs |
6 |
– | First tooth of mandible separated from second tooth by small incision (Figs |
9 |
6 | Ovipositor sheath approx. as long as hind tibia; first tergite 1.6–2.0 × longer than its apical width | 7 |
– | Ovipositor sheath 1.4 × longer than hind tibia; first tergite at most 1.5 × longer than its apical width | 8 |
7 | First flagellomere ~ 2 × longer than wide; second flagellomere 1.6 × longer than first flagellomere; notauli not reaching medio-posterior depression; vein 3-SR 1.6 × longer than 2-SR; antenna without whit segments | P. fidelis Fischer, 1970 |
8 | Second flagellomere 2 × longer than first flagellomere (Fig. |
P. tanycauda Sohn & van Achterberg, sp. nov. |
– | Second flagellomere 1.4 × longer than first flagellomere (Fig. |
P. setosa Sohn & van Achterberg, sp. nov. |
9 | First flagellomere 2.8–3.6 × longer than wide | 10 |
– | First flagellomere 4.2–5.1 × longer than wide (Figs |
13 |
10 | Eye in dorsal view 4.0–4.5 × as long as temple; propleuron reddish brown; notauli reduced posteriorly | P. artotemporalis Sohn & van Achterberg, 2021 |
– | Eye in dorsal view 2.0–3.0 × as long as temple; propleuron black or orange-brown; notauli usually complete (up to medio-posterior depression or nearly so) | 11 |
11 | Mandible subparallel-sided; setose part of ovipositor sheath ~ 0.7 × as long as hind tibia; first metasomal tergite ~ 1.4 × longer than its apical width | P. brachyura Sohn & van Achterberg, 2021 |
– | Mandible distinctly widened dorsally; setose part of ovipositor sheath 1.2–1.3 × as long as hind tibia; first tergite 1.1–1.2 × longer than its apical width | 12 |
12 | Tarsal claws slender; third and fourth antennal segments dark brown and slender; metanotum more or less tooth-shaped protruding dorsally in lateral view; pterostigma ~ 4 × longer than wide; middle tooth of mandible not widened dorsally | P. masha Belokobylskij, 1998 |
– | Tarsal claws robust; third and fourth antennal segments yellow and robust; metanotum obtuse dorsally in lateral view; pterostigma ~ 5.5 × longer than wide; middle tooth of mandible widened dorsally | P. lobata Sohn & van Achterberg, 2021 |
13 | Precoxal sulcus distinct and complete, reaching anterior and posterior edge of mesopleuron, (Fig. |
P. acutidentata Sohn & van Achterberg, sp. nov. |
– | Precoxal sulcus only medially impressed, not reaching anterior and posterior edge of mesopleuron (Fig. |
14 |
14 | Mandible 1.2 × longer than its maximum width (Fig. |
P. angusticeps Sohn & van Achterberg, sp. nov. |
– | Mandible 1.6 × longer than its maximum width (Fig. |
15 |
15 | Vein r of fore wing short, ~ 1.4 × longer than wide, vein SR1 of fore wing straight (Fig. |
P. tacitoides Sohn & van Achterberg, sp. nov. |
– | Vein r of for wing ~ 3.0 × longer than wide, vein SR1 of fore wing slightly curved (Fig. |
P. tacita Stelfox, 1941 |
Holotype • ♀ (NIBR), South Korea, Mt. Odae, Jinbu-myeon, Pyeongchang-gun, Gangwon-do, 37°45'54.7"N, 128°34'13.8"E, 15.IX.2020, Ju-Hyeong Sohn leg. GenBank accession no. PP587250.
The new species is similar with P. telengai Belokobylskij, 1998, but recognizable the third tooth distinctly and acutely protruding as the first one (only second tooth narrow and acute in P. telengai), first flagellomere 4.2 × longer than wide (2.8–3.0 × in P. telengai) and hind femur 4.2 × longer than wide (4.7–5.0 × in P. telengai).
Holotype, ♀, body 2.8 mm in lateral view, fore wing 2.6 mm, ovipositor sheath 1.4 mm in lateral view, antenna 3.4 mm (apical part of antennae missing).
Head
: Width of head 1.5 × its median length in dorsal view (Fig.
Phaenocarpa acutidentata sp. nov., ♀ A habitus, lateral view B antennae C wings D head, dorsal view E head, frontal view F mesosoma, dorsal view G mesosoma, lateral view H first metasomal tergite, dorsal view I ovipositor sheath, lateral view J proximal part of antenna K mandible, lateral view L claw, lateral view.
Mesosoma
: In dorsal view mesosoma 2.2 × longer than wide 1.6 × longer than high in lateral view. Mesoscutum (Fig.
Leg : Hind femur 4.2 × longer than wide and 0.7 × as long as hind tibia; hind tibia 11 × longer than wide; hind tibia as long as hind tarsus.
Metasoma
: First tergite (Fig.
Color
: Body (Fig.
Male. Unknown.
Unknown.
Unknown.
South Korea.
The specific name acutidentata is an adjective, referring to ‘sharp teeth’ in Latin.
Holotype • ♀ (NIBR), South Korea, Mt. Kalbong, Gyeongban-ri, Gapyeong-eup, Gapyeong-gun, Gyeonggi-do, 37°51'10.9"N, 127°26'27.4"E, 11.V.2020, Sohn. GenBank accession no. PP587251.
Differs from the other Phaenocarpa species by vein r of fore wing being much more distal (1.4 × longer than wide). This species similar with P. tacita Stelfox, 1941, but easily distinguish by apical antennal segments paler than subbasal segments, and first tooth of mandible lobe-shaped, widened dorsally, 1.7 × as long as third (first tooth of mandible acute and as long as third tooth in P. tacita).
Holotype, ♀, body 1.7 mm in lateral view, fore wing 2.0 mm, ovipositor sheath 0.5 mm, antenna 1.5 mm.
Head
: Width of head 1.7 × its median length in dorsal view (Fig.
Phaenocarpa tacitoides sp. nov., ♀ A habitus, lateral view B antennae C wings D head, dorsal view E head, frontal view F mesosoma, dorsal view G mesosoma, lateral view H first metasomal tergite, dorsal view I ovipositor sheath, lateral view J proximal part of antenna K mandible, lateral view L claw, lateral view.
Mesosoma
: In dorsal view mesosoma 1.8 × longer than wide and 1.4 × longer than high in lateral view. Mesoscutum (Fig.
Leg : Hind femur slender, 5.6 × longer than wide and 0.6 × as long as hind tibia; hind tibia 19 × longer than wide; hind tibia as long as hind tarsus.
Metasoma
: First tergite (Fig.
Color
: Body (Fig.
Male. Unknown.
Unknown.
Unknown.
South Korea.
The specific name tacitoides is an adjective, named after P. tacita and -oides added a suffix because of its similarity to this species (“oides” is Latin for “resembling”).
Holotype • ♀ (NIBR), South Korea, Mt. Kalbong, Gyeongban-ri, Gapyeong-eup, Gapyeong-gun, Gyeonggi-do, 37°51'10.9"N, 127°26'27.4"E, 05.VI.2020, Sohn. GenBank accession no. PP587252.
This new species is close to P. micula Belokobylskij, 1998, because of sharing width of the first flagellomere (3.0–3.5 × in P. micula), deep and smooth notauli and width of the first tergite. However, the new species has the metanotum not protruding (tooth-like protruding in P. micula) (Fig.
Phaenocarpa setosa sp. nov., ♀ A habitus, lateral view B antennae C wings D head, dorsal view E head, frontal view F mesosoma, dorsal view G mesosoma, lateral view H first metasomal tergite, dorsal view I ovipositor sheath, lateral view J proximal part of antenna K mandible, lateral view L claw, lateral view.
Holotype, ♀, body 2.8 mm in lateral view, fore wing 2.7 mm, ovipositor sheath 1.3 mm, antenna 3.8 mm (but apical parts missing).
Head
: Width of head 1.7 × its median length in dorsal view (Fig.
Mesosoma
: In dorsal view mesosoma 2.0 × longer than wide and 1.4 × longer than high in lateral view. Mesoscutum (Fig.
Leg
: Hind femur 5.7 × longer than wide and 0.8 × as long as hind tibia; hind tibia 10 × longer than wide and setae erect except basally (Fig.
Metasoma
: First tergite (Fig.
Color
: Body (Fig.
Male. Unknown.
Unknown.
Unknown.
South Korea.
The specific name setos” is an adjective, named after the erect setae of the hind tibia.
Holotype • ♀ (NIBR), South Korea, Mt. Kalbong, Gyeongban-ri, Gapyeong-eup, Gapyeong-gun, Gyeonggi-do, 37°51'10.9"N, 127°26'27.4"E, 05.VI.2020, Sohn. GenBank accession no. PP587254.
This new species is close to P. chasanica Belokobylskij, 1998 because of sharing second flagellomere 1.4–1.5 × longer than first flagellomere (same length in P. chasanica). Width of head 1.8 × its median length in dorsal view (1.8–2.0 × in P. chasanica). In mandible, first and second tooth not separated distinctly. Hind femur 5.0–5.5 × as long as wide. The new species differs from P. chasanica by head and mesosoma black (head and mesosoma yellowish brown in P. chasanica) and thick and short tarsal claws (tarsal claws thin and relatively long in P. chasanica). The new species can be recognised by its comparatively long ovipositor sheath (1.2 × longer than mesosoma and 1.4 × longer than hind tibia) and rugose median part of face rugose.
Holotype, ♀, body 2.5 mm in lateral view, fore wing 2.5 mm, ovipositor sheath 1.0 mm, antenna 3.9 mm.
Head
: Width of head 1.8 × its median length in dorsal view (Fig.
Phaenocarpa tanycauda sp. nov., ♀ A habitus, lateral view B antennae C wings D head, dorsal view E head, frontal view F mesosoma, dorsal view G mesosoma, lateral view H first metasomal tergite, dorsal view I ovipositor sheath, lateral view J proximal part of antenna K mandible, lateral view L claw, lateral view.
Mesosoma
: In dorsal view mesosoma 1.9 × longer than wide and 1.4 × longer than high in lateral view. Mesoscutum (Fig.
Leg : Hind femur 5.4 × as long as wide and 0.7 × as long as hind tibia; hind tibia 8.8 × longer than wide; hind tibia 0.8 × as long as hind tarsus.
Metasoma
: First tergite (Fig.
Color
: Body (Fig.
Male. Unknown.
Unknown.
Unknown.
South Korea.
The specific name tanycauda is an adjective, named after the long ovipositor sheath; tanyo is Greek for stretched out, cauda is Latin for tail.
Holotype • ♀ (NIBR), South Korea, Gwaneumsa, Sanrokbuk-ro, Jeju-si, Jeju-do, 33°25'43.9"N, 126°33'24.8"E, 06.VII.2020, Sohn. GenBank accession no. PP587255.
Differs from all the species of Phaenocarpa by having narrow face, 0.9 × from ventral rim of antennal sockets to upper margin of clypeus (1.2–1.6 × in other species). Second flagellomere 1.1 × longer than first flagellomere (1.2–2.0 × in other species).
Holotype, ♀, body 2.4 mm in lateral view, fore wing 2.7 mm, ovipositor sheath 0.8 mm, antenna 3.5 mm.
Head
: Width of head 1.8 × its median length in dorsal view (Fig.
Phaenocarpa angusticeps sp. nov., ♀ A habitus, lateral view B antennae C wings D head, dorsal view E head, frontal view F mesosoma, dorsal view G mesosoma, lateral view H first metasomal tergite, dorsal view I ovipositor sheath, lateral view J proximal part of antenna K mandible, lateral view L claw, lateral view.
Mesosoma
: In dorsal view mesosoma 2.0 × longer than wide and 1.4 × longer than high in lateral view. Mesoscutum (Fig.
Leg : Hind femur 6.0 × as long as wide and 0.7 × as long as hind tibia; hind tibia 15 × as long as wide; hind tibia 1.1 × longer than hind tarsus.
Metasoma
: First tergite (Fig.
Color
: Body (Fig.
Male. Unknown.
Unknown.
Unknown.
South Korea.
The specific name angusticeps is an adjective, angustus is Latin for narrow, ceps is Latin for head.
Holotype • (NIBR), South Korea, Mt. Kalbongsan, Gyeongban-ri, Gapyeong-eup, Gapyeong-gun, Gyeonggi-do, 37°51'10.9"N, 127°26'27.4"E, 05.VI.2020, Sohn. GenBank accession no. PP587256.
According to the East Palaearctic key of
Phaenocarpa tacita Stelfox, 1941 ♀ A habitus, lateral view B antennae C wings D head, dorsal view E head, frontal view F mesosoma, dorsal view G mesosoma, lateral view H first metasomal tergite, dorsal view I ovipositor sheath, lateral view J proximal part of antenna K mandible, lateral view L claw, lateral view.
♀. Body 1.9 mm in lateral view, fore wing 2.1 mm, ovipositor sheath 0.9 mm, antenna 2.6 mm (apical parts missing).
Head
: Width of head 1.8 × its median length in dorsal view (Fig.
Mesosoma
: In dorsal view mesosoma 2.0 × longer than wide and 1.3 × longer than high in lateral view. Mesoscutum (Fig.
Leg : Hind femur 4.6 × longer than wide and 0.7 × as long as hind tibia; hind tibia 15 × longer than wide; hind tibia as long as hind tarsus.
Metasoma
: First tergite (Fig.
Color
: Body (Fig.
Male. Unknown.
Unknown.
Unknown.
Austria (
The genus Phaenocarpa in Korea is a large group with 231 species across nine subgenera, but only nine species were recorded in Korea until now. With the addition of five new and one European species, there are now 15 species of Phaenocarpa in Korea. The new species and Phaenocarpa artotemporalis Sohn & van Achterberg, 2021, P. brachyura Sohn & van Achterberg, 2021, and P. lobata Sohn & van Achterberg, 2021 are only recorded in Korea. Phaenocarpa masha Belokobylskij, 1998, is recorded in Russia and Korea, and P. fidelis Fischer, 1970, P. angustiptera Papp, 1968, and P. eunice (Haliday, 1838), are recorded in the eastern Palearctic region (
Unfortunately, all the species used in this study are females, and records of males have not yet been confirmed. However, males could be identified later using COI barcoding and identification keys.
The authors have declared that no competing interests exist.
No ethical statement was reported.
This work was supported by a grant from the National Institute of Biological Resources (NIBR), funded by the Ministry of Environment (MOE) of the Republic of Korea (NIBR202402202 and NIBRE202404). It was also supported by Basic Science Research Program through the National Research Foundation of Korea (NRF) funded by the Ministry of Education (2022R1A2C1091308).
Conceptualization: HK, JHS. Data curation: JHS, SK. Formal analysis: JHS. Funding acquisition: HK. Methodology: HK, JHS, CA, SK. Project administration: HK. Resources: JHS. Software: JHS, SK. Supervision: HK. Validation: HK, JHS, CA. Visualization: JHS. Writing - original draft: JHS, CA. Writing - review and editing: JHS, HK, CA.
Ju-Hyeong Sohn https://orcid.org/0000-0003-0976-4114
Cornelis van Achterberg https://orcid.org/0000-0002-6495-4853
Sangjin Kim https://orcid.org/0000-0001-8395-8019
Hyojoong Kim https://orcid.org/0000-0002-1706-2991
All of the data that support the findings of this study are available in the main text.