SciELO - Scientific Electronic Library Online

 
vol.30 número4El género Heteromphrale Krober, 1937 (Diptera; Scenopinidae) en Perú, con la descripción de una especie nuevaNotas de Anqasha picta (Pocock, 1903) y descripción de una especie nueva de Anqasha de Perú (Araneae, Theraphosidae, Theraphosinae) índice de autoresíndice de materiabúsqueda de artículos
Home Pagelista alfabética de revistas  

Servicios Personalizados

Revista

Articulo

Indicadores

  • No hay articulos citadosCitado por SciELO

Links relacionados

Compartir


Revista Peruana de Biología

versión On-line ISSN 1727-9933

Rev. peru biol. vol.30 no.4 Lima oct./dic. 2023  Epub 07-Dic-2023

http://dx.doi.org/10.15381/rpb.v30i4.26022 

Trabajos originales

A new species of Sesioctonus Viereck (Hymenoptera, Braconidae, Agathidinae) from Peru

Una Nueva especie de Sesioctonus Viereck (Hymenoptera, Braconidae, Agathidinae) del Perú

1. Universidad Nacional Mayor de San Marcos, Museo de Historia Natural, Departamento de Entomología, Lima, Perú, Dirección postal: 15072.

Abstract

A new species of Sesioctonus (Braconidae: Agathidinae), Sesioctonus alvaradae sp. nov. from Peru, is described and illustrated. With the addition of this new species, Sesioctonus genus has 36 species.

Key words: Insect; taxonomy; biodiversity; parasitoid; Neotropical

Resumen

Una nueva especie de Sesioctonus (Braconidae: Agathidinae), Sesioctonus alvaradae sp. nov. para Perú, es descrita e ilustrada. Con la adición de esta nueva especie, el género Sesioctonus tiene 36 especies.

Palabras claves: Insecto; taxonomía; biodiversidad; parasitoide; Neotropical

Introduction

SesioctonusViereck, 1912 is a Neotropical genus of the Agathidinae subfamily. Its biology is largely unknown, and the only species with a known host is S. parathyridis Viereck, 1912 recorded as a larval parasitoid of the moth Arrhenophanes perspicilla Stoll, 1790 (Lepidoptera, Arrhenophanidae) (Viereck 1912, 1914). Briceño (2003) revised the species of Sesioctonus and found 26 new species. Later, Sharkey and Briceño (2005) described five new species from Colombia, and Sulca and Sharkey (2012) described three new species from Peru. With the addition of this new species, Sesioctonus now comprises 36 species.

The majority of Sesioctonus species were collected between 100m and 2800 m above sea level, but S. philipiSharkey and Briceño 2005 was collected at 3350 m. The material used in this study comes from collections between 4000 - 4500m above sea level, representing the highest elevation records of the genus. Here I present the description of a new Andean species, and an extended key to Sesioctonus species of the world, modified from Sulca and Sharkey (2012).

Material and methods

Morphological terminology follows that of Sharkey and Wharton (1997) and the key to genera follows that of Sharkey et al. (2021). Figures mentioned in this paper that are followed by the letter ‘B’ refer to those in Briceño (2003). The species description is based on the holotype, with variation given in parenthesis. Specimens are deposited in the Museo de Historia Natural, Universidad Nacional Mayor de San Marcos (MUSM) collection in Lima, Peru.

Taxonomy and descriptions

SesioctonusViereck, 1912

Viereck 1912:1. Type species: Sesioctonus parathyridis Viereck. (Monobasic and original designation). Viereck 1914: 133.

Diagnosis. Sesioctonus species may be distinguished from other agathidines using the following combination of characters: Mesoscutum smooth, lacking notauli; tarsal claws simple, lacking a distinctive basal claw; hind coxal cavities open, sharing a common opening with the metasomal foramen.

Distribution. Members of Sesioctonus are restricted to the Neotropical Region.

List of all Sesioctonus species described

Sesioctonus acrolophusBriceño, 2003; S. alvaradae sp. nov; S. amazonensis Briceño, 2003; S. ammosakron Briceño, 2003; S. analogus Briceño, 2003; S. areolatus Briceño, 2003; S. ariasi Briceño, 2003; S. armandoi Briceño, 2003; S. binaSulca & Sharkey, 2012; S. biospleres Briceño, 2003; S. boliviensis Briceño, 2003; S. brasiliensis Briceño, 2003; S. chaconi Briceño, 2003; S. chrestos Briceño, 2003; S. clavijoi Briceño, 2003; S. diazi Briceño, 2003; S. dichromus Briceño, 2003; S. dominions Briceño, 2003; S. eumenetes Briceño, 2003; S. galeos Briceño, 2003; S. garciai Briceño, 2003; S. grandis Briceño, 2003; S. huggerti Sulca & Sharkey, 2012; S. kompsos Briceño, 2003; S. longinoi Sharkey & Briceño, 2005; S. miyayensis Briceño, 2003; S. parathyridisViereck, 1912; S. peruviensis Briceño, 2003; S. philipi Sharkey & Briceño, 2005; S. qui Briceño, 2003; S. theskelos Briceño, 2003; S. venezuelensis Briceño, 2003; S. torresi Sharkey & Briceño, 2005; S. stephaniai Sharkey & Briceño, 2005; S. susanai Sharkey & Briceño, 2005 and S. wayquecha Sulca & Sharkey, 2012.

Key to Sesioctonus species of the world modified from Sulca & Sharkey (2012)

1. Occipital tubercles present (Figs. 16B-18B) 2

― Occipital tubercles absent. (Figs. 19B)17

2(1). Epicnemial carina straight medially or absent, not indented at midline, between forecoxae) (Figs. 4B, 23B) 3

― Epicnemial carina bilobed medially, (indented at midline, between forecoxae) (Figs. 3B, 22B)6

3(2) Epicnemial carina complete laterally (Figs. 3B, 22B) 4

― Epicnemial carina incomplete or absent laterally (Fig. 23B) 5

4(3) Interantennal space with longitudinal rounded keel, face without median longitudinal carinae garciai Briceño

― Interantennal space lack of longitudinal keel, face with median longitudinal carinae huggertii Sulca & Sharkey

5(3) Face with median longitudinal carina (Fig. 13B) acrolophus Briceño

― Face without median longitudinal carina (similar to Figs. 12B,14B) analogus Briceño

6(3) Midcoxa not completely melanic, color variable7

― Midcoxa completely melanic10

7(6) Forewing banded from base: yellow, black, yellow, black chaconi Briceño

― Forewing infuscate (melanic)8

8(7) Fore tibias with spines; mid femur yellowish orange 9

― Fore tibia without spines; mid femur melanic longinoi (part) Sharkey & Briceño

9(8) Median longitudinal carinae of propodeum absent, median areola of metanotum and with lateral carinae not meeting posteriorly, subpronope triangular peruviensis Briceño

― Median longitudinal carinae of propodeum present, median areola of metanotum and with lateral carinae meeting posteriorly, subpronope oval bina Sulca & Sharkey

10(6) Longitudinal carina(e) of scutellar depression present and forewing banded from base: yellow, black, yellow, black venezuelensis Briceño

― Longitudinal carina(e) of scutellar depression absent and/or forewing not banded11

11(10) Mesoscutum black; median areola of metanotum with longitudinal rugosities (Fig. 29B); median tergite of first metasomal segment without pair of lateral longitudinal carinae (similar to Fig. 34B); forewing (RS+M)a vein complete (Fig. 10B) kompsos Briceño

― Mesoscutum yellowish orange; or if black then not combining other character12

12(11) Mesoscutum melanic 13

― Mesoscutum yellowish orange14

13(12) Forewing infuscate with large hyaline spot; metasoma reddish brown except last few segments melanic brasiliensis Briceño

― Forewing either infuscate without hyaline spot or hyaline basally, infuscate apically; metasoma yellowish orange dichromus Briceño

14(12) Median longitudinal carina of propodeum present and complete ariasi Briceño

― Median longitudinal carina of propodeum absent or incomplete15

15(14) Subpronope triangular, three sides almost equal (Fig. 1B); forewing 3RSa vein absent (Fig. 10B) boliviensis Briceño

― Subpronope more oval-shaped, weak triangle with vertical sides longer than dorsal side (Fig. 2B); forewing 3RSa vein present (Fig. 9B)16

16(15) Wings banded from base: yellow, black, yellow, black diazi Briceño

― Wings infuscate (melanic) longinoi (part) Sharkey & Briceño

17(1) Occiput excavated (similar to Figs. 16B-18B) 18

― Occiput not excavated (Fig.19B)19

18(17) Propodeum with central areola absent; Epicnemial carina bilobed medially (between forecoxae) (similar to Fig.3B) eumenetes Briceño

― Propodeum with central areola present (Fig.7); Epicnemial carina straight medially (between forecoxae) (Fig.8). alvaradae sp. nov.

19(17) Interantennal space without sharp longitudinal keel 20

― Interantennal space with sharp longitudinal keel (Fig. 11B) 35

20(19) Basal sterna of metasoma chalk-white 21

― Basal sterna of metasoma not chalk-white, rather melanic or yellowish orange 23

21(20) Head orange susanai Sharkey & Briceño

― Head black 22

22(21) Fore and hind coxa pale yellow stephaniai Sharkey & Briceño

― Fore and hind coxa melanic philipi Sharkey & Briceño

23(20) Median areola of metanotum with lateral carinae meeting posteriorly (Figs. 25B, 26B) 24

― Median areola of metanotum with lateral carinae absent or, if present, not meeting posteriorly (Figs. 27B, 28B)33

24(23) Epicnemial carina present (Figs. 3B, 4B) 25

― Epicnemial carina absent 29

25(24) Epicnemial carina complete laterally (Fig. 3B)26

― Epicnemial carina incomplete laterally (Fig. 4B) 31

26(25) Hind tibia melanic amazonensis Briceño

―Hind tibia mostly yellowish orange27

27(26) Propodeum with central areola absent28

― Propodeum with central areola present areolatus Briceño

28(27) Antenna with more than 29 flagellomeres; interantennal space with rounded longitudinal keel (similar to Fig. 12B); hind tibia yellowish orange in basal half, melanic apically miyayensis Briceño

― Antenna with less than 28 flagellomeres; interantennal space without longitudinal keel; hind tibia mostly yellowish orange, melanic apically clavijoi Briceño

29(24) Scutellar depression with longitudinal carinae; body color yellow, white, and black torresi Sharkey & Briceño

― Scutellar depression without longitudinal carinae; body color yellowish orange and black 30

30(29) (RS+M)a vein of forewing complete, median tergite of first metasomal segment with pair of lateral longitudinal carinae ammosakron Briceño

― (RS+M)a vein forewing incomplete, median tergite of first metasomal segment without pair of lateral longitudinal carinae wayquecha Sulca & Sharkey

31(25) Epicnemial carina straight medially (between forecoxae) (Fig. 4B); body length less than 3mm dominicus Briceño

― Epicnemial carina bilobed medially (indented at midline, between forecoxae) (Fig. 3B); body length more than 3mm32

32(31) Forewing (RS+M)a vein complete (Fig. 10B) armandoi Briceño

Forewing (RS+M)a vein incomplete (Fig. 9B) biospleres Briceño

33(23) Epicnemial carina present complete, or incomplete laterally (Figs. 3B, 4B)34

― Epicnemial carina completely absent chrestos Briceño

34(35) Forewing banded, yellow, black, yellow, black; labial palpus 3-segmented galeos Briceño

― Forewing infuscate; labial palpus 4-segmented theskelos Briceño

35(19) Third and fourth labial palpomeres not fused; first metasomal median tergite with depression posterad spiracle (Figs. 36B, 37B) grandis Briceño

― Third and fourth labial palpomeres fused, first metasomal median tergite with or without depression posterad spiracle36

36(35) First metasomal median tergite with depression posterad spiracle (similar to Figs. 3B, 36B) qui Briceño

― First metasomal median tergite without depression posterad spiracle parathyridis Viereck

Sesioctonus alvaradae sp. nov.

(Fig. 1-8)

Holotype. 1♀, PERU: AP [APURIMAC]: Mina Las Bambas, Sector Sagrapeña, 14o4’37.24’’S/ 72o18’33’’W, 4265 m, 01.iii.2020, L. Pérez.

Paratype. 3♀, PERU: AP: Mina Las Bambas, Sector Sagrapeña, 14o4’37.4’’S/ 72o18’33’’W, 4265 m, 07- 10.xii.2019, L. Pérez; 4♀, PERU: AP: Mina Las Bambas, Sector Sagrapeña, 14o4’37.4’’S/ 72o18’33’’W, 4265 m, 20-24. i.2021, R. Angulo; 1♀, PERU: AP: Mina Las Bambas, Sector Sagrapeña, 14o4’37.4’’S/ 72o18’33’’W, 4265 m, 03-10.iii.2021, R. Angulo; 2♀, PERU: AP: Mina Las Bambas, Sector Sagrapeña, 14o4’37.24’’S/ 72o18’33’’W, 4265 m, 02.x.2020, Y. Nina; 2♀, PERU: AP: Mina Las Bambas, Sector Sagrapeña, 14o4’37.11’’S/ 72o18’32.63’’W, 4178 m, 21- 23.ii.2019, L. Pérez; 2♀PERU: AP: Mina Las Bambas, Sector Sagrapeña, 14o4’37.24’’S/ 72o18’33’’W, 4265 m, 29.xi-03.xii.2018, L. Pérez; 3♀, PERU: AP: Cotabambas, Challhuahuacho, Pumamarca (Sallahue), 14o2’56.53’’S/ 72o19’19’’W, 4291 m, 03-04. iii.2020, N. Zenteno y A. Silva; 1♀, PERU: AP: Cotabambas, Challhuahuacho, Pumamarca (Sallahue), 14o3’6.1’’S/ 72o18’39.9’’W, 4201 m, 03-04. iii.2020, N. Zenteno y A. Silva; 1♀, PERU: AP: Cotabambas, CC Antuyo, 14o4’32.89’’S/ 72o16’46.25’’W, 4353 m, 6. iii.2020, N. Zenteno y A. Silva; 1 ♀, PERU: AP: Cotabambas, Challhuahuacho, Ferrobamba, 14o5’18.5’’S/ 72o20’51.01’’W, 4376 m, N. Zenteno y A. Silva; 1 ♀, PERU: AP: Gran Progreso, 14o1’30.24’’S/ 72o26’6.85’’W, 4029 m, 25.vii.2021, N. Zenteno y A. Silva; 1 ♀, PERU: AP: Chalcobamba, 14o3’38.86’’S/ 72o20’20.42’’W, 4509 m, 25.viii.2019, L. Perez; 1 ♀, PERU: AP: Cotabambas, Challhuahuacho, Ferrobamba, 14o3’28.6’’S/ 72o19’55.72’’W, 4438 m, 17.x.2021, L. Villena; 1 ♀, PERU: AP: Cotabambas, Challhuahuacho, CCPP. Cconchaccota, 14o11’17.6’’S/ 72o4’5.4’’W, 4438 m, 12- 13.iii.2015, L. Sulca & I. Medina; 1 ♀, PERU: AP: Cotabambas, Challhuahuacho, CCPP. Ccahuanhuire, 14o10’34.5’’S/ 72o23’52.8’’W, 4079m, 13- 14.iii.2015, L. Sulca & I. Medina; 1 ♀, PERU: CU: Paruro, Omacha, 14o8’26.7’’S/ 71o53’17.1’’W, 4178m, 1- 5.iii.2022, A. Nuñez; 1 ♀, PERU: CU: Chumbivilca, Uchucarco, 14o23’29.64’’S/ 71o47’6.72’’W, 4544m, 16.ix.2022, A. Ayala; 1 ♀, PERU: CU: Espinar, Mina Constancia, 13o33’54’’S/ 71o42’41’’W, 4309m, 15-23.ix.2017, L. Huerto.

Diagnosis. Distinguished from all other known species of Sesioctonus by the following combination of characters: occipital tubercles absent, occiput excavated, gena moderately expanded posteroventrally, subpronope elongate-oval, epicnemial carina complete and straight medially, propodeum with a central areola.

Sesioctonus alvaradae sp. nov. is similar to S. eumenetes, as they are the only two species that have an occiput excavated; but the first one has a central areola on the propodeum that is lacking in S. eumenetes.

Briceño (2003) indicates in the S. eumenetes diagnosis the presence of a median longitudinal carina on the propodeum, but contradicts the description indicating absence. I was able to verify the absence of a longitudinal carina by reviewing the photos of the S. eumenetes holotype hosted in the website of the Canadian National Collection ( https://www.cnc.agr.gc.ca/taxonomy/Specimen.php?id=5878).

♀ Length. Length of body, excluding ovipositor, 4.1 mm.

Figures 1 6. Details of Sesioctonus alvaradae sp. nov. Holotype:(1) habitus; (2) head, frontal; (3) head, dorsal; (4), metasomal tergo (5); mesonotum, dorsal; (6) propodeum and metasomal terga 1-2. 

Head. Flagellum with 23 flagellomeres. Interantennal space lacking longitudinal keel. Antennal sockets not excavated. Face without median longitudinal carina. Gena moderately expanded posteroventrally. Occipital tubercles absent. Occiput excavated. Mandible concave, outer tooth of mandible not longer than inner tooth. Maxillary palpus with 4 palpomeres. Third and fourth labial palpomeres not fused. Mesosoma. Subpronope elongate-oval. Longitudinal carinae of scutellar depression absent. Scutellum convex. Median areola of metanotum smooth; without median longitudinal carina; and with lateral carinae meeting posteriorly. Propodeum convex, with a central areola. Epicnemial carina complete, straight medially (between forecoxae). Foretibial spines present. Midtibia with 8 spines. Hind tibia with 8 spines. Hind femur 4 times as long as wide. (RS+M)a vein of forewing incomplete. 3RSa vein of forewing absent. 2-1A vein of hind wing tubular. Cub vein of hind wing absent. Hind wing with 3 hamuli. Metasoma. Median tergite of first metasomal segment with pair of lateral longitudinal carinae. First metasomal median tergite without depression postered spiracle. Length/width ratio of first metasomal median tergite 1.5. Ovipositor 3.7 mm. Color. Head melanic. Antenna melanic. Maxillary palpomeres melanic. Labial palpomeres melanic. Mandible yellowish with melanic teeth. Mesosoma mostly melanic except mesoscutum orangish red with two spots melanic around of tegulae and mesopleuron, anterior scutellum, middle of metapleuron orangish red. Legs mostly melanic except yellowish orange at apical of femur; basal 1/3 melanic and apical 2/3 yellowish orange. Forewing entirely infuscate. Stigma melanic. Hind wing entirely infuscate. First metasomal tergum melanic. Second metasomal tergum yellowish orange. Third metasomal tergum yellowish orange. Fourth metasomal tergum yellowish orange. Fifth and sixth metasomal terga yellowish orange with melanic spot. Seventh and to eighth metasomal terga melanic. Ovipositor yellowish orange.

Figures 7 8. Details of Sesioctonus alvaradae sp. nov. Paratype:(7) Propodeum with central areola present (indicated by arrow); (8) Epicnemial carina straight medially (indicated by arrow). 

Male. As in the female (above) with the color of the metasomal terga slightly different. First metasomal tergum melanic. Second metasomal tergum yellowish orange. Third -to fifth metasomal terga yellowish orange with melanic spot. Sixth and to eighth metasomal terga melanic.

Variation. Legs with variable color, but always melanic to yellow. Sometimes propodeum with a yellow spot medially.

Etymology. Named in honor of Mabel Alvarado, a Peruvian specialist in ichneumonoid wasps, for her support during the author’s entomological studies.

Distribution. Known only from Apurimac and Cusco, in southeastern Peru.

Agradecimientos / Acknowledgments:

The author is grateful to Gerardo Lamas, Michael Sharkey, Mabel Alvarado, Luis Figueroa, and Lita Inga whose support was essential to the completion of this work. Also, thanks to Eduardo Shimbori and an anonymous reviewer for valuable comments that enhanced the manuscript.

Literature cited

Briceño GRA. 2003. Taxonomic Revision of the Genus Sesioctonus Viereck (Hymenoptera: Braconidae: Agathidinae). Journal of Hymenoptera Research. 12:238-271. [ Links ]

Sharkey MJ, Janzen DH, Hallwachs W, Chapman EG, Smith MA, Dapkey T, Brown A, Ratnasingham S, Naik S, Manjunath R, et al. 2021. Minimalist revision and description of 403 new species in 11 subfamilies of Costa Rican braconid parasitoid wasps, including host records for 219 species. ZooKeys. 1013:1-665. https://doi.org/10.3897/zookeys.1013.55600 [ Links ]

Sharkey MJ, Briceño-G R. 2005. Review of Sesioctonus Viereck (Hymenoptera: Braconidae: Agathidinae) from Colombia with descriptions of five new species. Zootaxa. 1002(1):45. https://doi.org/10.11646/zootaxa.1002.1.3. [ Links ]

Sharkey MJ, Wharton RA. 1997. Morphology and terminology. In: Manual of the New World genera of the family Braconidae (Hymenoptera). Washington D. C.: The International Society of Hymenopterists. p. 19-38. [ Links ]

Sulca L, Sharkey MJ. 2012. Three new species of Sesioctonus Viereck (Hymenoptera, Braconidae, Agathidinae) from Peru. Zookeys. 196:1-10. https://doi.org/10.3897/zookeys.196.3086 [ Links ]

Viereck HL. 1914. Type species of the genera of ichneumon flies. Bulletin of the United States National Museum. i-v, 1-186 [accessed 2023 Jun 6]. http://repository.si.edu/xmlui/handle/10088/10232Links ]

Viereck HL. 1912. New genus and species of Hymenoptera of the family Braconidae from Panama. Smithsonian miscellaneous collections. 59(5):1-2. https://repository.si.edu/handle/10088/23460Links ]

Publicación registrada en Zoobank/ZooBank article registered: LSIDurn:lsid:zoobank.org:pub:27DF6B6F-86FD-4E30-8D13-ED78ACFE0B3E

Acto nomenclatural/nomenclatural act: Sesioctonus alvaradae Sulca, 2023 LSIDurn:lsid:zoobank.org:act:BF4457F1-FEEF-4A50-B51B-AEE728B368C9

Publicación registrada en Zoobank/ZooBank article registered: LSIDurn:lsid:zoobank.org:pub:27DF6B6F-86FD-4E30-8D13-ED78ACFE0B3E

Acto nomenclatural/nomenclatural act: Sesioctonus alvaradae Sulca, 2023 LSIDurn:lsid:zoobank.org:act:BF4457F1-FEEF-4A50-B51B-AEE728B368C9

Fuentes de financiamiento / Funding: The author declares that this research did not receive any specific grant from any funding agency, from the commercial or non-profit sector.

Aspectos éticos / legales; Ethics / legals: The authors declare that they have not violated or omitted ethical or legal norms when carrying out the research and this work.

Citación Sulca L. 2023. New species of Sesioctonus Viereck (Hymenoptera, Braconidae, Agathidinae) from Peru. Revista peruana de biología 30(4): e26022 - 000 (Diciembre 2023). doi: https://dx.doi.org/10.15381/rpb.v30i4.26022

Editor: Diana Silva

Received: August 16, 2023; Accepted: November 15, 2023

*Corresponding author lidia.sulca@gmail.com

Conflicto de intereses / Competing interests: The author declares no conflict of interest.

Rol de los autores / Authors Roles: LS: Conceptualization; Formal analysis; Investigation; Writing-Preparation of the original draft; Drafting: review and editing.

Creative Commons License This is an open-access article distributed under the terms of the Creative Commons Attribution License