Research Article |
Corresponding author: John T. Huber ( john.huber2@agr.gc.ca ) Academic editor: Petr Janšta
© 2022 John T. Huber, Jennifer D. Read.
This is an open access article distributed under the terms of the CC0 Public Domain Dedication.
Citation:
Huber JT, Read JD (2022) Three new genera of Mymaridae (Hymenoptera) from the Neotropical region. Journal of Hymenoptera Research 92: 1-21. https://doi.org/10.3897/jhr.92.81917
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Three new genera and species of Mymaridae from the Neotropical region are described: Megamymar waorani Huber, gen. and sp. nov.; Neopolynemoidea chilensis Huber, gen. and sp. nov.; and Porcepicus herison Huber, gen. and sp. nov. Their possible relationships are discussed to place them in context among the previously described genera of Mymaridae.
fairyflies, new genera and species, South America, taxonomy
Mymaridae are a relatively large family of Hymenoptera, at present including about 100 valid genera, 90 of them extant and 10 extinct, including 2 fossils that may be misplaced in Mymaridae. This is almost double the number treated in the only world key (
Specimens were point or card mounted and photographed. Because of its large size, the specimen representing the first genus and species was retained on a point mount and photographed using a ProgRes C14plus digital camera mounted on a Nikon SMZ1500 microscope; its description and, especially, measurements are therefore not as accurate as for the other two species. One specimen of each of the other two species was dissected and slide mounted in Canada balsam. These specimens were photographed at different focal planes using the same camera as above mounted on a Nikon Eclipse E800 compound microscope, and the resulting layers combined and refined using Zerene StackerTM. The layers were edited from the top of the focus stack down to produce one image showing surface structures. For certain views, such as posterior or ventral, the layers were combined and edited from the bottom up. These views were flipped either horizontally or vertically in Adobe Photoshop to appear as if the specimen was photographed from that surface. A unique image number is given to different structures but if different planes of the same structure (from the same individual) are illustrated, e.g., of the metasoma (Fig.
fl = flagellar segment (in males), fu = funicular segment (in females), gt = gastral tergum, LOL = distance between a lateral ocellus and median ocellus, mps = multiporous plate sensillum, OOL =distance between a lateral ocellus and eye margin, POL = distance between lateral ocelli. The specimen depositories are:
Megamymar waorani Huber, here designated.
With the following combination of features: body huge (for a fairyfly), together with exserted section of the ovipositor well over 9 mm long; median ocellus abutting transverse trabecula; petiole distinctly shorter than gaster and, in dorsal view, completely hidden; metatarsus 1 longer than metatibia; gaster extending as horn anterodorsal to mesosoma.
Female. Head. Head slightly wider than mesosoma (21: 20), ~1.4× as wide as long, ~1.1× as wide as high and almost 1.25× as high as long, measured laterally; transverse trabecula entirely dark; supraorbital trabecula with well sclerotized (dark) anterior half short, extending posteriorly only to level of posterior margin of median ocellus, then continuing posteriorly as poorly sclerotized (light) section extending as far as anterior margin of lateral ocellus and further continuing obliquely towards but not reaching occipital foramen as a faint, fine line. Face ~0.5× as wide as high, in lateral view upper face receding to transverse trabecula and lower face flat and, in anterior view, with distinct depression medially dorsal to oral cavity and short, narrow vertical depression ventral to torulus; torulus ~0.5× its own height from transverse trabecula; preorbital sulci slightly converging medially just ventral to toruli then continuing straight ventrally to dorsolateral angle of oral cavity. Compound eye slightly shorter than malar space and apparently with very few short setae among the ommatidia. Vertex in lateral view slightly curved, posteriorly merging smoothly with occiput; median ocellus abutting transverse trabecula; POL 2.0× LOL and ~1.7× OOL. Gena ventrally in lateral view longer than eye length but dorsally much shorter. Back of head without sulci and oral cavity well separated from occipital foramen. Antenna. Scape with radicle barely differentiated; funicle 6-segmented; clava 1-segmented. Mouthparts. Mandibles apparently with 3 teeth, meeting when closed. Mesosoma. Mesosoma almost 2.6× as long as wide, almost 3.2× as long as high, and ~0.8× as wide as high. Pronotum entire, in lateral view almost horizontal, with flat dorsum, in dorsal view triangular and, including neck, almost as long as mesoscutum. Prosternum ~1.3× as long as wide, and entire. Mesoscutum just over 2.0× as long as scutellum + frenum, in lateral view flat; notauli incomplete, ~0.3 as long as mesoscutum as measured from their junction with anterior margin. Scutellum ~4.0× as long as poorly defined frenum; axilla barely advanced, each ~1.0× as wide as long. Metanotum slightly longer than frenum, without obvious dorsellum. Propodeum slightly longer than scutellum + frenum, with a shallow and narrow longitudinal median depression, in lateral view almost horizontal; spiracle in a shallow wide depression. Wings. Fore wing fairly wide, with apex rounded and slightly asymmetrical, and with almost straight margin behind venation; venation ~0.2× as long as wing length; parastigma with proximal but apparently without distal macrochaetae, with hypochaeta next to proximal macrochaeta. Hind wing narrow and almost straight. Legs. Legs long; tarsi 4-segmented, with tarsomere 1 of all legs longer than tibiae. Metasoma. Metasoma ~2.3× as long as mesosoma (Fig.
Male. Unknown.
A euphonious combination from Greek: megas, meaning large, and Mymar, the name of the type genus of Mymaridae. The genus name is neuter. Mega refers to the large body of the only known species of the genus, which is over 1 mm longer than the next longest Neotropical species, Erdosiella mira (Annecke & Doutt), whose body length is 3.7 mm.
Megamymar is best placed in Mymarini sensu
Megamymar superficially resembles several of the largest species of Australomymar Girault and the extralimital genera Borneomymar Huber, Neotriadomerus Huber and Paranaphoidea Girault. At least some species in all these genera, none of which are mophologically closely related to Megamymar, have a long ovipositor often greatly exserted posteriorly (Australomymar, Borneomymar, Polynemoidea Girault) or anteriorly (Neotriadomerus). In the Neotropical region, Australomymar appears superficially to be the most similar looking genus but the body of the largest species is at most ~3.0 mm long and the base of the female gaster does not extend anteriorly in a dorsal horn (the gastral sac). In other genera of Mymaridae the ovipositor may extend anteriorly but it is always ventral to the mesosoma.
Holotype female (USNM) on triangular card point labelled 1. “ECUADOR: NAPO Res. Ethnica Waorani, 1km S. Onkone Gare Camp, Trans.Ent. 9 Oct. 1994 220m 00°39'10"S, 76°26'W T.L. Erwin et al.”. 2. “Holotype Megamymar waorani Huber”. 2. “Insecticidal fogging of mostly bare green leaves, some with covering of lichenous or bryophytic plants in terra firme forest. At Trans 5m Sta. 4 Project MAXUS Lot 913” 3. “HOLOTYPE f# Megamymar waorani Huber”.
Megamymar waorani is the only described species in the genus. Its diagnosis is therefore the same as for the generic description, i.e., ovipositor extending anteriorly in a short, truncate gastral sac dorsal to propodeum (Fig.
Female. Colour. Body orange-yellow, with metasoma except for apical tergum and sternum slightly lighter; transverse trabecula and mandibles dark reddish-brown; scape and pedicel dark yellow, fu1–fu4 brown except slightly lighter apex of fu4, fu5 cream coloured, fu6 and clava dark brown; legs same colour as body except mesotibia slightly darker yellow, mesotarsomere brown, and metatibia and tarsus almost black. Fore wing clear except yellowish suffusion posterior to and slightly distal to venation; hind wing clear (Fig.
The species is named after the indigenous Waorani people of Ecuador in whose reserve M. waorani was collected. Their way of life has been seriously affected by resource extraction and settlement by colonists. The species name is treated as a noun in apposition.
Unknown, but because of its size, likely a solitary parasitoid in large insect eggs. We suggest that the host is most likely a species of Orthoptera. First, despite M. waorani being the third longest fairyfly species known worldwide, after specimens of a species of Neotriadomerus from Australia and specimens of one species of Australomymar from New Zealand, it has apparently never been collected at ground level, despite considerable Malaise or pan trapping in equatorial rain forests of the Neotropical region. Second, the host egg must be at least 4.8 mm long and eggs of this size are mostly likely to be found among species of Orthoptera. Third, although hosts of any species of Mymaridae with body length over 3.0 mm are unknown, one relatively small (~1.3 mm) species of Australomymar has been reared from Tettigoniidae (Orthoptera) and one large (2.5 mm) species of Acmopolynema Ogloblin has been reared from Oecanthus spp. (Orthoptera: Gryllidae).
Neopolynemoidea chilensis Huber, here designated.
Female with the following combination of features: toruli almost touching transverse trabecula (Fig.
Female. Head. Head slightly wider than mesosoma (24: 21), ~1.8× as wide as long, ~1.6× as wide as high and almost 1.2× as high as long, measured laterally; transverse trabecula entire (Fig.
Male. Unknown.
From Greek: Neo- meaning new, referring to its occurrence in the New World and Polynemoidea, a monotypic genus known so far only from Tasmania. The name Neopolynemoidea is given to draw attention to the general similarity the two genera, one from the Old World and one from the New World.
Neopolynemoidea differs from Polynemoidea by: toruli almost in contact with transverse trabecula (separated from transverse trabecula by almost its own height in Polynemoidea), scape over 10× as long as wide (no more than 3× as long as wide in Polynemoidea); fore wing venation at least 0.6× as long as fore wing length (no more than 0.4 as long as fore wing length in Polynemoidea).
Worldwide, at least 14 genera or subgenera of Mymaridae have females with a 3-segmented clava: Allanagrus Noyes & Valentine, Allarescon Noyes & Valentine, Eustochomorpha Girault, Krokella Huber, Nesomymar Valentine, Nesopatasson Valentine, Neostethynium Ogloblin, Notomymar Doutt & Yoshimoto, Paracmotemnus Noyes & Valentine, Paranaphoidea (Idiocentrus) Gahan, Platystethynium (Platystethynium) Ogloblin, Polynemoidea, Pseudanaphes Noyes & Valentine, and Stethynium Enock. Except for Eustochomorpha, with an 8-segmented funicle in females, all have a 6-segmented funicle. The majority of these genera occur in the southern hemisphere, particularly in the southernmost areas, though several extend well into the northern hemisphere. Two other genera appear to have the clava with 3-segments in at least one species: one Eustochus (Eustochus) from China was described as having 3-segmented clava (the other described species have a 2-segmented clava) but this may be an artefact of partial antennal collapse, giving the appearance of a third segment; and Kompsomymar Huber, with a single described species from Australia, appears to have only partial divisions separating the claval segments. The hosts and biology of all but one (Stethynium) of the above genera are unknown. Among these, Krokella, Paracmotemnus and Polynemoidea have a fore wing venation longer than half the wing length, as in Neopolynemoidea, but none have the extremely long scape in females. Females of the only described species of Polynemoidea, however, have a long, exerted ovipositor. Therefore, based wing venation and ovipositor features a close relationship of Neopolynemoidea to Polynemoidea is proposed as being the most probable.
Holotype
female (CNC) in Canada balsam on slide (Fig.
Neopolynemoidea chilensis is the only described species in the genus so its diagnosis the same as for the generic description.
Female. Colour. Uniformly brown; scape, pedicel and legs except coxae and metafemur brownish yellow. Fore wing with brown suffusion except for a small clear area distal to stigma, a larger triangular area along posterior margin, a clear area anterior to retinaculum and a small one posterior to parastigma (Fig.
Unknown.
Porcepicus herison Huber, here designated.
Female with the following combination of features: back of head dorsal to foramen with median vertical occipital groove and transverse occipital groove/trabecula extending from eye to eye (Fig.
Female. Head. Head slightly narrower than mesosoma (14:17), ~2.0× as wide as long, ~1.7× as wide as high and ~1.15× as high as long, measured laterally; transverse and supraorbital trabeculae with short dark sections alternating with light sections. (Fig.
Porcepicus herison Huber, holotype female 12a head, anterior 12b head, posterior (seen through head and flipped horizontally) 13a right antenna (clava and fu5 missing) 13b right antenna (opposite surface seen through antenna and flipped horizontally) 14a left antenna 14b left antanna (opposite surface seen through antenna) 15 fore wing 16 hind wing 17 holotype slide.
Male. Unknown.
An arbitrary combination of letters based on the French word for porcupine, porc-épique, referring to the long and strong setae distributed on the antenna, body, and legs.
Porcepicus belongs to the Camptoptera group of genera. It appears to be most similar to Camptoptera by the back of the head having a vertical occipital groove, transverse occipital groove, and narrow and curved fore wing and lack of a hypochaeta. The 6-segmented funicle in females, slightly dorsoventrally flattened mesosoma, gaster wider than long, and apparent absence of a petiole distinguishes it from Camptoptera Foerster as well as the other genera in the genus group.
Holotype
female (CNC) in Canada balsam on slide (Fig.
Paratypes : Four females. PERU. Same locality data as holotype (2 females on cards, CNC); Junín River, NW of San Ramón, Río Oxabamba, San Fernan Farm, 925 m, 11°5'36"S, 75°23'43"W, 30.vi.2010, M. Hoddle, MT [Malaise trap] (1 female on slide, UCRC, UCRC ENT 285052); San Martín, 19 km NE Tarupoto, 950 m, 6–8.vii.2004, B. V. Brown, MT (1 female on point, UCRC, UCRC ENT 457917).
Porcepicus herison is the only described species in the genus so its diagnosis is the same as for the generic description.
Female. Colour. Body brown (mesoscutum light brown in one paratype) except anterior surface of gt1 white; legs light brown, pedicel and tarsi almost white; thick setae and their sockets on body, antenna and legs dark brown (Figs
The name is an arbitrary combination of letters similar to the French word for hedgehog, hérisson. The name is treated as a noun in apposition.
Unknown. As with most species in the Camptoptera group of genera the hosts are unknown. We suggest the hosts are Coleoptera based on at least one record from that order for Camptoptera and one for Litus.
The fairyfly fauna of the Neotropical region is one of the most diverse in the world, with about 50 genera, taking into account synonymies and genera added since
We thank the late T. Erwin, National Museum of Natural History, Washington, DC, for allowing the senior author to sort through some of the rich canopy fogging material he obtained over many years of collecting in Neotropical forests. Much remains to be sorted for Mymaridae, however, so perhaps more specimens of M. waorani may still be found in the collected material. We also thank K. Bolte (retired from Natural Resources Canada) who took the photograph of the holotype of M. waorani. We thank S. Triapitsyn (UCRC) for recognizing two specimens of P. herison in UCRC and recommending their addition to the type series.