ISSN 1911-2173

Key to the New World genera of Telengaiinae (formerly Gnamptodontinae) (Hymenoptera: Ichneumonoidea: Braconidae) and synopses of the genera

Accepted: April 01, 2025

Michael Sharkey

Hymenoptera Institute, 1100 Pepperhill Circle, Lexington, Kentucky 40502, USA, [email protected].

Key to the New World genera of Telengaiinae (formerly Gnamptodontinae) (Hymenoptera: Ichneumonoidea: Braconidae) and synopses of the genera

Key to the New World genera of Telengaiinae (formerly Gnamptodontinae) (Hymenoptera: Ichneumonoidea: Braconidae) and synopses of the genera

Accepted: April 01, 2025

Michael Sharkey

Hymenoptera Institute, 1100 Pepperhill Circle, Lexington, Kentucky 40502, USA, [email protected].

Abstract

This is an updated overview of the New World (Western Hemisphere) members of Telengaiinae (= Gnamptodontinae). It is a revision of the key by Wharton (1997) (as Gnamptodontinae). It includes a key to the New World genera and a synopsis of each genus. The synopses include the following sections: diagnosis, biology, diversity, distribution, publications, and notes. There are five genera in the New World, two reported here for the first time, and seven genera worldwide.

Gnamptodon sp., Lexington, Kentucky, U.S.A.

Wharton, R.A. 1997. Subfamily Gnamptodontinae, pp.256–259. In: Wharton, R.A., Marsh, P.M., & Sharkey, M.J. (eds). Manual of the New World Genera of the Family Braconidae (Hymenoptera). Special Publication of the International Society of Hymenopterists, 439 pp.

Introduction

This treatment of the New World genera of Telengaiinae is part of a comprehensive effort to treat all New World genera of Braconidae. To confirm a subfamily identification the key by Sharkey et al. (2023) may be used. Readers using that key will be automatically directed here if they obtain an identification of Telengaiinae. The present work includes a key to the five New World genera and a synopsis of each genus.

Telengaiini was erected for the monotypic genus, Telengaia Tobias, from Turkmenistan (Tobias 1962), as a tribe of Exothecinae. Molecular data in Jasso-Martinez et al. (2022a) showed that Telengaia is derived within Telengaiinae (as Gnamptodontinae), and since the family-group name Telengaiini has priority, they synonymized Gnamptodontinae under Telengaiinae. This relationship was recognized by Tian et al. (2020) though they did not synonymize the two subfamilies. Wharton (1997) included Exodontiella in the key to Alysiinae due to the exodont mandibles. Two exclusively Old World genera, Telengaia and Gnaptogaster Tobias, are included in the subfamily.

The use of the names Gnamptodon Haliday and Gnamptodontinae (rather than the previously used Gnaptodon and Gnaptodontinae) is based on Opinion 1424 (1987) of the Commission on Zoological Nomenclature. Fischer (1972, 1977, 1981) included Liparophleps Enderlein (= Plesademon Fischer) in the Telengaiinae (as Gnamptodontinae). However, Wharton (1997) referring to a series of specimens from Costa Rica confirmed the sexually dimorphic nature of the wing vein pattern and concurred with Marsh (1976) that Liparophleps is a synonym of Semirhytus Szépligeti and belongs in Doryctinae.

General morphological terminology can be found in Sharkey et al. (2023). More detailed information is in the morphology chapter of the New World manual (Sharkey and Wharton, 1997) and in the Hymenoptera Anatomy Ontology Portal (http://portal.hymao.org/projects/32/public/ontology/).

Overview of subfamily

Phylogeny

Zaldívar-Riverón et al. (2006) recovered Telengaiinae in a clade consisting of Telengaiinae, Exothecinae, Alysiinae, Opiinae, and Braconinae in most analyses, with Gnamptodontini and Telengaiini resolved as sister taxa. Exodontiella Wharton was recovered with Gnamptodontini in all analyses and, therefore, Wharton et al. (2006) transferred it to Telengaiinae (as Gnamptodontinae) from Opiinae. Jasso-Martínez et al. (2022a) using ultraconserved elements (UCEs) recovered the grouping Braconinae (Telengaia + Gnamptodontini). Employing mitochondrial phylogenomics Jasso-Martínez et al. (2022b) recovered the same relationship between Telengaia and Gnamptodontini but these were sister to (((Alysiinae + Opiinae) Exothecinae) Braconinae). The genera have not been phylogenetically analyzed and this is sorely needed. For example, the primary or perhaps sole difference between Gnamptodon Haliday and Pseudognaptodon Fisher is the presence or absence of crossvein 2r-m of the forewing. This character varies from completely absent, to barely indicated as a small anterior stub, to complete. Neognamptodon and Tamdaona are recorded here for the first time from the New World. The New World specimens may constitute new genera though they fit the diagnoses of their respective genera. Whether or not Neognamptodon Belokobylskij and Tamdaona Belokobylskij are valid genera is also open to question because they differ primarily on the presence or absence of a short and incomplete portion of the occipital carina.

Biology

Telengaiines are primarily parasitoids of leaf-mining lepidopterans of Nepticulidae (van Achterberg, 1983; Shaw and Huddleston, 1991; Whitfield and Wagner, 1991; Yu et al., 2016) but also attack Gracillariidae (Balevski and Tomov, 1997). They are apparently koinobiont parasitoids (Shaw and Huddleston, 1991; Quicke, 2015) but It is not known whether they are endo- or ectoparasitoids.

Common genera

Gnamptodon, Neognamptodon, and Pseudognaptodon are moderately common though Neognamptodon is rare in the Nearctic. They are composed of rather small specimens (1–3 mm,) and are easily overlooked by collectors. There are currently (Nov. 24, 2024) 47 Barcode Index Number (BINs, proxies for species) in the Barcode of Life Data System (BOLD) from Costa Rica divided among Gnamptodon, Neognamptodon, Pseudognaptodon, and Tamadaona suggesting that there are hundreds of undescribed species of these genera in the New World. Most of the New World species of Neognamptodon, and Tamadaona on BOLD are identified as Gnamptodon at the time of this writing (Nov. 25, 2024).

Distribution

Cosmopolitan.

Distinguishing features

Exodontiella has exodont mandibles (Fig. 1E) and unique forewing venation (Fig. 1B) that distinguish it from all other New World braconids. All other telengaiines are characterized by the presence of a well-defined line or groove delimiting a basal-median, somewhat rectangular area, on the second metasomal tergum. This basal-median area is described in some publications as a raised swelling or elevation (Figs 2D, 3D, 4D, 5D), but in several species, it is flat. Additionally, all species are quite small (often less than 2mm), lack an epicnemial carina, and often lack an occipital carina.

Note. All images are by M. Sharkey.

Checklist

Table 1. List of New World genera of Telengaiinae Tobias. New records for the New World are marked with an asterisk.

 Exodontiella Wharton, 1978

 Gnamptodon Haliday, 1873

 Neognamptodon Belokobylskij, 1999*

 Pseudognaptodon Fisher, 1977

 Tamdaona Belokobylskij, 1994*

Key to genera

Key to the New World genera of Telengaiinae
Clicking the hyperlinked text in the key below will take the reader to the corresponding couplet or genus synopsis.
1.
A. RS vein of forewing ending next to apex of stigma. Mandibles exodont (teeth facing outward).
B. RS vein of forewing ending far from apex of stigma; second submarginal cell (2SM) not closed apically by the r-m crossvein. Mandibles endodont (teeth facing inward).
C. RS vein of forewing ending far from apex of stigma; second submarginal cell (2SM) closed apically by the r-m crossvein. Mandibles endodont (teeth facing inward).
Figure for couplet 1
2(4).
A. Propodeum lacking an anteromedial carina.
B. Propodeum with an anteromedial carina.
Figure for couplet 2
3(2).
A. Occipital carina present laterally.
B. Occipital carinae completely absent.
Figure for couplet 3

Generic treatments

Exodontiella Wharton, 1978

Diagnosis. Mandibles exodont (teeth facing laterally and mandibles not touching when closed) (Fig. 1E). RS vein of forewing meeting margin of wing immediately next to stigma (Fig. 1B).

Biology. Unknown.

Diversity. Two described species, several more undescribed are in the collection of the Hymenoptera Institute.

Distribution. Nearctic.

Figure 1. Exodontiella deserticola Wharton.

Gnamptodon Haliday, 1837

Diagnosis. Forewing with second submarginal cell (SSC) closed distally (Fig. 2C). Propodeum lacking an anteromedial carina (couplet 2A).

Biology. There are numerous records of rearings from Nepticulidae (Lepidoptera) (Yu et al, 2016) and one record from Gracillariidae (Lepidoptera) (Balevski and Tomov, 1997).

Diversity. Seven Nearctic and one Neotropical species are described.

Distribution. Worldwide.

Publication. Fisher (1977) treated the eight known New World species.

Figure 2. Gnamptodon sp.

Neognamptodon Belokobylskij, 1999

Diagnosis. Forewing with second submarginal cell (SSC) closed distally (Fig. 3B). Propodeum with an anteromedial carina (couplet 2B). Occipital carina completely absent (couplet 3B).

Biology. Unknown, but presumably leaf-mining Lepidoptera.

Diversity. No New World species are described.

Distribution. Nearctic, Neotropical, Oriental, Afrotropical (Madagascar), Australian (Papua New Guinea). This is the first report of the genus in the New World. In the New World, the genus is much more diverse in the Neotropics, and rare in the Nearctic.

Publications. Belokobylskij (1999) erected the genus and described two species. Van Achterberg (in Tian et al. 2020) described one species from the Oriental region and included a key to all species.

Notes. Almost all New World species have the apical tergites pinched towards the mid-line (Fig. 5D). This is not known in the Old World fauna and suggests that the New World species with this feature represent a separate lineage.

Figure 3. Neognamptodon sp.

Pseudognaptodon Fisher, 1977

Diagnosis. Second submarginal cell of forewing not closed apically (Fig. 4B). Apex of RS vein of forewing reaching wing margin remote from apex of stigma (Fig. 4B).

Biology. Reared from Nepticulidae, but no specific host records have been published (Fischer, 1977)

Diversity. There are 28 described New World species.

Distribution. Widespread in the New World and recorded from the Palearctic and Oriental regions (Tian et al., 2020).

Publications. Cirelli et al. (2002) described eight species of Pseudognaptodon from Brazil and provided a key to New World species. Williams (2004) described 17 species of Pseudognaptodon from the New World and divided the genus into two species groups (omissus-group and curticauda-group). A key to New World species was provided but did not include the species described in Cirelli et al. (2002). Van Achterberg (in Tian et al., 2020) renamed two of Williams’ species which were primary homonyms.

Figure 4. Pseudognaptodon sp.

Tamdaona Belokobylskij, 1994

Diagnosis. Forewing with second submarginal cell (SSC) closed distally (Fig. 5D). Propodeum with an anteromedial carina (couplet 2B). Occipital carina present laterally (couplet 3A).

Biology. Unknown, but presumably parasitoids of leaf-mining Lepidoptera.

Diversity. No New World species are described.

Distribution. Previous records are from the Oriental region; here we report species of Tamdaona from the Neotropical, and Australian (Papua New Guinea) regions for the first time.

Publications. Belokobylskij (1994) erected the genus. Van Achterberg (in Tian et al., 2020) described two new species and provided a key to the four known species, all from the Oriental region.

Figure 5. Tamdaona sp.

Acknowledgements

We thank Mostafa Ghafouri Moghaddam and A.P. Ranjith for their reviews of the submitted manuscript and the editors of CJAI for their efforts and patience.

References

Balevski, N., and Tomov, R. 1997. Mining moths from family Bucculatricidae, Nepticulidae and Tischeriidae (Lepidoptera) as hosts of parasitoids from family Braconidae (Hymenoptera). Acta Entomologica Bulgarica, 1-2: 114-119. (In Russian)

Belokobylskij, S.A. 1994. Contribution to the fauna of the Indo-Malayan braconid wasps of the tribe Exothecini, Pambolini and Pentatermini (Hymenoptera, Braconidae). Trudy Zoologicheskogo Instituta, 245: 125–173.

Belokobylskij, S.A., 1999. New genera of the subfamilies Rhyssalinae, Exothecinae and Gnamptodontinae from the Old World (Hymenoptera: Braconidae). Zoosystematica Rossica, 8:155-169. https://www.zin.ru/journals/zsr/content/1999/zr_1999_8_1_Belokobylskij.pdf

Cirelli, K.R.N., Braga, S.M.P, and Penteado-Dias, A.M. 2002. New species of Pseudognaptodon Fischer (Hymenoptera: Braconidae: Gnamptodontinae) from Brazil. Zoologische Mededelingen Leiden, 76: 89-96. https://repository.naturalis.nl/pub/217465/ZM76_089-096.pdf

Fischer, M. 1972. Hymenoptera Braconidae (Opiinae I), Das Tierreich, 91: 1-621.

Fischer, M. 1977. Hymenoptera Braconidae (Opiinae II-Amerika), Das Tierreich, 96: 1-1001.

Fischer, M. 1981. Eine neue Synonymie bei den Opiinae (Hymenoptera, Braconidae). Zeitschrift der Arbeitsgemeinschaft österreicher Entomologen, 32:136.

Jasso-Martínez, J.M., Santos, B.F., Zaldívar-Riverón, A., Fernández-Triana, J.L., Sharanowski, B.J., Richter, R., Dettman, J.R., Blaimer, B.B., Brady, S.G., and Kula, R.R. 2022a. Phylogenomics of braconid wasps (Hymenoptera, Braconidae) sheds light on classification and the evolution of parasitoid life history traits. Molecular Phylogenetics and Evolution, 173, p.107452.  https://www.sciencedirect.com/science/article/am/pii/S1055790322000653

Jasso-Martínez, J.M., Quicke, D.L., Belokobylskij, S.A., Santos, B.F., Fernández-Triana, J.L., Kula, R.R., and Zaldívar-Riverón, A. 2022b. Mitochondrial phylogenomics and mitogenome organization in the parasitoid wasp family Braconidae (Hymenoptera: Ichneumonoidea). BMC Ecology and Evolution, 22, p.46. https://doi.org/10.1186/s12862-022-01983-1

Marsh, P.M. 1976. Pars 13. Braconidae 9, Doryctinae.P. 1331. In: Vecht, J. van der and Shenefelt, R.D. (Eds.). Hymenopterorum Catalogus (nova editio). Dr. W. Junk, The Hague.

Opinion 1424. 1987. Gnamptodon Haliday, 1833 (Insecta, Hymenoptera): Bracon pumilio Nees, 1834 designated as type species. Bulletin of Zoological Nomenclature, 44: 55-56.

Quicke, DLJ. 2015. The braconid and ichneumonid parasitoid wasps: Biology, systematics and ecology. Wiley Blackwell, 681pp.

Sharkey, M.J., and Wharton, R.A. 1997. Morphology and terminology, pp.19-37. In: Wharton, R.A., Marsh, P.M., and Sharkey, M.J. (eds). Manual of the New World Genera of the Family Braconidae (Hymenoptera). Special Publication of the International Society of Hymenopterists, 439 pp.

Sharkey, M., Athey, K.J., Fernández-Triana, J.L., Penteado-Dias, A.M., Monckton, S.K., and Quicke, D.L., 2023. Key to the New World subfamilies of the family Braconidae (Hymenoptera: Ichneumonoidea). Canadian Journal of Arthropod Identification, 49: 1-43. https://doi.org/10.3752/cjai.2023.49

Shaw, M.R., and Huddleston, T. 1991. Classification and biology of braconid wasps (Hymenoptera: Braconidae). Handbooks for the Identification of British Insects, 7(11): 1-126. https://www.royensoc.co.uk/shop/publications/out-of-print-handbooks/vol-7-part-11-classification-biology-of-braconid-wasps-hymenoptera-braconidae/

Tobias, V.I. 1962. A new subfamily of Braconids (Hymenoptera, Braconidae) from Central Asia. Trudy Zoologicheskogo Instituta. Akad. Nauk SSSR, 30:268-270.

Tian, X.X., Wu, J.X., van Achterberg, C., and Tan, J.L. 2020. New Gnamptodontinae (Hymenoptera: Braconidae) from China and Vietnam, with two genera new for China and seven new species. Zootaxa, 4778: 471-508. https://doi.org/10.11646/zootaxa.4778.3.3

van Achterberg, C. 1983. Revisionary notes on the subfamily Gnaptodontinae, with description of eleven new species (Hymenoptera, Braconidae). Tijdschrift voor Entomologie, 126: 25-57.

Wharton, R.A. 1978. Exodontiellini, a new tribe of Opiinae with exodont mandibles. Pan-Pacific Entomologist, 53: 297-303.

Wharton, R.A. 1997. Gnamptodontinae: pp. 257-260. In: Wharton, R.A., Marsh, P.M. & Sharkey, M.J. “Manual of the New World genera of the family Braconidae (Hymenoptera).” International Society of Hymenopterists. Special Publication No. 1: 1-439.

Wharton, R.A., Yoder, M.J., Gillespie, J.J., Patton, J.C., and Honeycutt, R.L. 2006. Relationships of Exodontiella, a non-alysiine, exodont member of the family Braconidae (Insecta, Hymenoptera). Zoologica Scripta, 35: 323-340. https://www.academia.edu/download/49451601/Relationships_of_Exodontiella_a_nonalysi20161008-7536-ffkzq0.pdf

Whitfield, J.B., and Wagner, D.L. 1991. Annotated key to the genera of Braconidae (Hymenoptera) attacking leaf-mining Lepidoptera in the Holarctic Region. Journal of Natural History, 25: 733-754. https://www.researchgate.net/profile/David-Wagner/publication/238317983_Annotated_key_to_the_genera_of_Braconidae_Hymenoptera_attacking_leafmining_Lepidoptera_in_the_Holarctic_Region/links/549a1c6e0cf2d6581ab158d2/Annotated-key-to-the-genera-of-Braconidae-Hymenoptera-attacking-leafmining-Lepidoptera-in-the-Holarctic-Region.pdf

Williams, D.J. 2004. Revision of the genus Pseudognaptodon Fischer (Hymenoptera: Braconidae: Gnamptodontinae). Journal of Hymenoptera Research, 13: 149-205. https://www.biodiversitylibrary.org/page/2844810

Yu, DS, Achterberg, C van, Horstmann, K. 2016. World Ichneumonoidea 2011. Taxonomy, Biology, Morphology and Distribution. USB Flash drive. Taxapad, Ottawa, Canada. www.taxapad.com.

Zaldívar-Riverón, A., Mori, M., and Quicke, D.L.J. 2006. Systematics of the cyclostome subfamilies of braconid parasitic wasps (Hymenoptera: Ichneumonoidea): a simultaneous molecular and morphological Bayesian approach. Molecular Phylogenetics and Evolution, 38: 130-145. https://www.sciencedirect.com/science/article/pii/S1055790305002599?casa_token=0mKEGpnSnUsAAAAA:C6sO46M33qeou0yzi5yCZLA8v0_OjJ5IwSBKxRLVUe8NHrtm-UI8sf0vm_LUTmP479mfKlrDAA