57 research outputs found

    Three new species of Dolichogenidea Viereck (Hymenoptera, Braconidae, Microgastrinae) from Australia with exceptionally long ovipositors

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    The subfamily Microgastrinae contains an extraordinarily rich diversity of parasitoid wasps which parasitise larval lepidopterans. The Australian fauna has generally been poorly studied, particularly for the very speciose genera. One such genus is Dolichogenidea Vierek, which in Australia is known from only six described species. Here we describe three new species of Dolichogenidea from Australia, which are distinguished by possessing extremely long ovipositors compared with the typical form for the genus. These are D. finchi Fagan-Jeffries & Austin, sp. n., D. mediocaudata Fagan-Jeffries & Austin, sp. n., and D. xenomorph Fagan-Jeffries & Austin, sp. n. In describing these new species we also discuss relationships within the genus, and the diversity and biology of the Australian fauna

    Cotesia kazak

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    <i>Cotesia kazak</i> (Telenga, 1949) <p>Figs 8A, 18B, E</p> <p> <i>Apanteles kazak</i> Telenga, 1949: 385 (lectotype, ♀, ZIN).</p> <p> <i>Cotesia kazak</i> – Papp 1988: 153 (transfer from <i>Apanteles</i> s.l.).</p> Diagnosis <p> <i>Cotesia kazak</i> can be separated from all other species of <i>Cotesia</i> currently described from Australia and Papua New Guinea by the following combination of characters: anteromesoscutum punctulate, smoother than most species; T3 densely setose; fore wing 2RS not creating a ‘stub’ at junction with r; T1 parallel sided.</p> Material examined <p> <b>Other material</b></p> <p> AUSTRALIA – <b>Western Australia</b> • 2 ♀♀; “ Maraginiup ” [Mariginiup]; 20 Mar. 1990; P. Hutchinson leg.; ex. <i>Heliothis</i> on Lucerne; emerged 2 Apr. 1990; <i>Cotesia kazak</i> determined A. Austin 1990; WINC • 1 ♂; Carabooda; 1 Mar. 1990; S. Harrington leg.; ex. <i>Heliothis</i> on Lucerne; emerged 9 Mar. 1990; <i>Cotesia kazak</i> determined A. Austin 1990; WINC • 4 ♀♀, 2 ♂♂; Wokalup RS [Research Station]; 17 Feb. 1988; P. Lawrence leg.; ex. <i>Heliothis punctiger</i>; <i>Cotesia kazak</i> determined A. Austin 1990; WINC.</p> Distribution <p> Palearctic. Introduced to WA (Michael <i>et al.</i> 1984) and New Zealand (Carl 1978; Cameron & Valentine 1985) for the biological control of <i>Helicoverpa armigera</i> (Hübner, 1808).</p> Host <p> <i>Helicoverpa armigera</i> (Noctuidae) (record from description and biological control literature), solitary (le Masurier 1987). <i>Helicoverpa punctigera</i> (Wallengren, 1860), solitary (from examined material).</p>Published as part of <i>Fagan-Jeffries, Erinn P. & Austin, Andrew D., 2020, Synopsis of the parasitoid wasp genus Cotesia Cameron, 1891 (Hymenoptera: Braconidae: Microgastrinae) in Australia, with the description of seven new species, pp. 1-70 in European Journal of Taxonomy 667 (667)</i> on page 27, DOI: 10.5852/ejt.2020.667, <a href="http://zenodo.org/record/3899324">http://zenodo.org/record/3899324</a&gt

    Cotesia rubecula

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    <i>Cotesia rubecula</i> (Marshall, 1885) <p>Figs 7B, 23 C–D</p> <p> <i>Apanteles rubecula</i> Marshall, 1885: 175 (holotype, ♀, NHMUK).</p> <p> <i>Cotesia rubecula</i> – Mason 1981: 113 (transferred from <i>Apanteles</i> s.l.).</p> <p> For a full bibliography, see Shenefelt (1972: 615), Yu <i>et al</i>. (2016) and Fernández-Triana <i>et al.</i> (2020).</p> Diagnosis <p>T1 consistently broadening posteriorly, often with a middle patch of rugosity on posterior smooth band of scutellum (under scutellar triangular disk); scutellar disk with only shallow punctures; mesosoma not dorsoventrally flattened; hind coxa and metasoma dark; ocelli normal sized, OOL/posterior ocellus diameter <2.4; fore wing vein r normally longer than, occasionally of similar length to 2RS; distal quarter of hind tibia darkened, including in lateral view.</p> Material examined <p> AUSTRALIA • 3 ♀♀, 7 ♂♂; South Australia, Urrbrae; 27 Feb. 1987; M.A. Keller leg.; on broccoli ex. cocoon; <i>Apanteles rubecula</i> det A. D. Austin 1987; WINC • 2 ♀♀; South Australia, Adelaide; reared in culture; 1 Aug. 1989; M.A. Keller leg.; “ <i>Cotesia rubecula</i> ”; WINC.</p> Distribution <p> Europe (type). Introduced into Australia and New Zealand (Wilson 1960; Cameron & Walker 2002). For global distribution, see Fernández-Triana <i>et al.</i> (2020).</p> Host <p> <i>Pieris rapae</i> (Pieridae). Solitary. Record from original description. See Shenefelt (1972: 615) and Yu <i>et al</i>. (2016) for extra-limital host records.</p> Remarks <p> This species forms a distinct clade in the <i>COI</i> phylogeny (Fig. 1) using sequences available on BOLD from outside of Australia. No Australian specimens were sequenced in this study.</p>Published as part of <i>Fagan-Jeffries, Erinn P. & Austin, Andrew D., 2020, Synopsis of the parasitoid wasp genus Cotesia Cameron, 1891 (Hymenoptera: Braconidae: Microgastrinae) in Australia, with the description of seven new species, pp. 1-70 in European Journal of Taxonomy 667 (667)</i> on pages 44-45, DOI: 10.5852/ejt.2020.667, <a href="http://zenodo.org/record/3899324">http://zenodo.org/record/3899324</a&gt

    Cotesia wonboynensis Fagan-Jeffries & Austin 2020, sp. nov.

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    <i>Cotesia wonboynensis</i> sp. nov. <p>urn:lsid:zoobank.org:act: 67EECA2C-26A3-401A-A0A7-98B6DF264677</p> <p>Figs 10B, 32</p> Diagnosis <p> <i>Cotesia wonboynensis</i> sp. nov. can be separated from all other species of <i>Cotesia</i> currently described from Australia and Papua New Guinea by the following combination of characters: T2 ovoid, occasionally semicircle shaped, with very strong, wide crenulate border; scutoscutellar sulcus with approximately 9–11 pits; T1 parallel sided; T3 dark with sparse setae on most of tergite; anteromesoscutum sculpturing punctate reticulate; scutellar disk smooth with shallow punctures associated with setae; centre of medial posterior band of the scutellum smooth; fore wing 2RS not creating a ‘stub’ at junction with r.</p> Etymology <p>This species is named for the town Wonboyn, from where the type series was collected and reared by Paul Whitington and Kerri-Lee Harris.</p> Material examined <p> <b>Holotype</b></p> <p> AUSTRALIA • ♀; NSW, Wonboyn; 37.24417° S, 149.90306° E; emerged 25 Mar. 2019; P. Whitington and K-L. Harris leg.; reared from <i>Anthela s</i> p., cf <i>A. connexa</i>, on <i>Allocasuarina littoralis</i> (Salisb.) L.A.S.Johnson; BOLD (for co-reared specimen): AUMIC539-19; Genbank <i>COI</i> (for co-reared specimen): MN182700; ANIC 32 130294.</p> <p> <b>Paratypes</b></p> <p>AUSTRALIA • 3 ♀♀, 1 ♂; same collection data as for holotype; ANIC 32 130295 to 130298 • 1 ♀, 1 ♂; same collection data as for holotype; WINC.</p> Description <p> <b>Female</b></p> <p>COLOUR. Head, antenna and mesosoma and dorsal metasoma other than non-sclerotised areas of T1 dark; anterior sternites pale, darkening posteriorly; (fore-, mid-, hind coxa) dark, dark, dark; femora (fore-, mid-, hind femur) pale, pale, pale darkening distally; tibiae (fore-, mid-, hind tibia) pale, pale, light brown darkening distally; tegula and humeral complex dark; pterostigma dark; fore wing veins dark.</p> <p>BODY LENGTH. Head to apex of metasoma: 2.7 (2.4–2.7) mm.</p> <p>HEAD. Antenna slightly longer than body length; OOL/posterior ocellus diameter 2.0 (2.0–2.1); POL/ posterior ocellus diameter 1.8 (1.7–1.9); antennal flagellomere 2 length/width 3.0 (3.3–3.4); antennal flagellomere 14 length/width 3.0 (2.7–3.2).</p> <p>MESOSOMA. Anteromesoscutum sculpturing punctate reticulate, reasonably regular but less dense and shallower in centre and on lateral sides; number of pits in scutoscutellar sulcus 9 (9, 11); scutellar disc with only shallow pits associated with setae and no basal rugostiy; maximum height of mesoscutellum lunules/maximum height of lateral face of mesoscutellum 0.52 (0.55).</p> <p>WINGS. Fore wing length 2.8 (2.4–2.8) mm; length of veins r/2RS 0.9; length of veins 2RS/2M 1.3 (1.5–1.6); length of veins 2M/(RS+M)b 1.6 (1.2); pterostigma length/width 2.9 (2.6–3.1).</p> <p>LEGS. Hind tibia inner spur length/metabasitarsus length 0.5 (0.5–0.6).</p> <p>PROPODEUM. Medial carina distinct, rest of propodeum rugose, in paratypes with stronger, less dense carinae and smoother posterio-lateral corners.</p> <p>METASOMA. T1 length / T1 width at posterior margin 1.6; parallel sided, irregularly punctured in posterior third; T2 width at posterior margin /T2 length 1.7, semicircle shaped, almost ovoid in holotype, irregularly sculptured with strong crenulate border on all sides, T2 length / T3 length 0.7; T3 sculpture smooth and shiny; ovipositor sheaths length/hind tibial length 0.1 (0.15–0.17).</p> <p> <b>Male</b></p> <p>As female, only slight variations in measurements.</p> Host <p> <i>Anthela</i> sp., most likely <i>A. connexa</i> (Walker, 1855) (Anthelidae) (identification from image of larvae by E.P. Beaver).</p> Distribution <p>Currently known only from type locality on the southern NSW coastal region, although as the host occurs throughout the east coast of Australia and into Tasmania, this parasitoid is likely to have a wider range than is currently known.</p>Published as part of <i>Fagan-Jeffries, Erinn P. & Austin, Andrew D., 2020, Synopsis of the parasitoid wasp genus Cotesia Cameron, 1891 (Hymenoptera: Braconidae: Microgastrinae) in Australia, with the description of seven new species, pp. 1-70 in European Journal of Taxonomy 667 (667)</i> on pages 59-61, DOI: 10.5852/ejt.2020.667, <a href="http://zenodo.org/record/3899324">http://zenodo.org/record/3899324</a&gt

    Cotesia scripta Fagan-Jeffries & Austin 2020, sp. nov.

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    <i>Cotesia scripta</i> sp. nov. <p>urn:lsid:zoobank.org:act: 9512A1E2-9BCD-48E2-85AC-5CDBA7FBC5A8</p> <p>Figs 10D, 11B, 29</p> Diagnosis <p> <i>Cotesia scripta</i> sp. nov. can be separated from all other species of <i>Cotesia</i> currently described from Australia and Papua New Guinea by the following combination of characters: fore wing vein r subtly curved; fore wing 2RS not creating a ‘stub’ at junction with vein r; anteromesoscutum punctate reticulate; scutellar disk smooth, or with only shallow punctures associated with setae and centre of medial posterior band of the scutellum smooth; T1 parallel sided; border between T2 and T3 smoothly indented; T3 dark with sparse setae on posterior two thirds.</p> Etymology <p>This species is derived from the Latin for ‘write’ as an acknowledgement of The University of Adelaide Environment Institute funded Early-Mid Career Researcher writing retreat, on which this paper was partially compiled. It is a feminine nominative singular adjective.</p> Material examined <p> <b>Holotype</b></p> <p> AUSTRALIA • ♀; Victoria, Mount Eliza; emerged Feb. 2018; R. Standen leg.; reared from <i>Epicoma constristis</i> on <i>Calistomon</i> sp.; collection code B9; BOLD: AUMIC540-19 (for co-reared specimen), Genbank <i>COI</i> (for co-reared specimen): MN182696; MV T22495.</p> <p> <b>Paratypes</b></p> <p> AUSTRALIA • 3 ♀♀, 1 ♂; same collection data as for holotype; MV T22495-9 • 2 ♀♀; same collection data as for holotype; WINC • 4 ♀♀, 1 ♂; Victoria, Mount Eliza; emerged Feb. 2018; R. Standen leg.; reared from <i>Epicoma contristis</i> Hübner, 1823 on <i>Calistomon</i> sp.; collection code B14; BOLD: AUMIC541-19 (for co-reared specimen), Genbank <i>COI</i> (for co-reared specimen): MN182698; MV T22500-4 • 1 ♀; same collection data as for preceding; WINC • 3 ♂♂; Victoria, Mount Eliza; emerged Apr. 2019; R. Standen leg.; reared from <i>Epicoma</i> sp. <i>on Thyrptomene</i> sp.; collection code B13; BOLD: AUMIC542-19 (for co-reared specimen), Genbank <i>COI</i> (for co-reared specimen): MN182701; MV T22505-7.</p> Description <p> <b>Female</b></p> <p>COLOUR. Head and mesosoma and dorsal metasoma other than non-sclerotised areas of T1 dark; anterior sternites pale, darkening posteriorly; (fore-, mid-, hind coxa) dark, dark, dark; femora (fore-, mid-, hind femur) pale/orange, pale/orange, pale/orange with dark patch distally; tibiae (fore-, mid-, hind tibia) pale/orange, pale/orange, pale/orange darkening distally; tegula and humeral complex light brown; pterostigma dark; fore wing veins dark.</p> <p>BODY LENGTH. Head to apex of metasoma: 3.1 (3.0) mm.</p> <p>HEAD. Antennae broken in all female type specimens; OOL/posterior ocellus diameter 2.3 (2.5); POL/ posterior ocellus diameter 2.2 (2.2–2.5); antennal flagellomere 2 length/width missing in holotype (2.5); antennal flagellomere 14 missing in all specimens.</p> <p>MESOSOMA. Anteromesoscutum sculpturing punctate reticulate, reasonably regular but less dense and shallower in centre and on lateral sides; number of pits in scutoscutellar sulcus 12 (10); scutellar disc with only shallow pits associated with setae and no basal rugostiy; maximum height of mesoscutellum lunules/maximum height of lateral face of mesoscutellum 0.6 (0.5).</p> <p>WINGS. Fore wing length 3.0 (2.7– 3.0) mm; length of veins r/2RS 0.8 (0.9–1.0); length of veins 2RS/2M 1.6 (1.5–1.7); length of veins 2M/(RS+M)b 1.0 (0.8–0.9); pterostigma length/width 2.3 (2.5).</p> <p>LEGS. Hind tibia inner spur length/metabasitarsus length 0.6 (0.5–0.6).</p> <p>PROPODEUM. Medial carina distinct in holotype but can be faint or nearly undiscernible in paratypes, rest of propodeum mostly smooth, some scattered rugosity and small carinae in posterior centre, posterior lateral corners, sometimes with anterior transverse carinae.</p> <p>METASOMA. T1 length /T1 width at posterior margin 1.4; parallel sided, mostly smooth; T2 width at posterior margin/T2 length 2.4 (2.1–2.5), semicircle to trapezoid shaped, mostly smooth, in some specimens with scattered rugosity, T2 length /T3 length 0.6 (0.6–0.8); T3 sculpture smooth and shiny; ovipositor sheaths length/hind tibial length 0.13 (0.12–0.18).</p> <p> <b>Male</b></p> <p>As female, only slight variations in measurements, T2 thinner and stronger sculptured with strong indented border.</p> Host <p> <i>Epicoma contristis</i> Hübner, 1823 (Notodontidae), gregarious.</p> Distribution <p>Currently only known from the type locality on the Mornington Peninsula, Victoria. The host species is found throughout Australia, suggesting the wasp likely also has a wider distribution range than currently known.</p> Remarks <p>All specimens of this species, including the holotype, are not complete specimens, but the presence of DNA barcodes and host data warranted the description of this species regardless of the incompleteness of the description (missing the flagellomere 14 measurements) and poor condition of the type series. Measurements given of paratypes in description n = 2.</p>Published as part of <i>Fagan-Jeffries, Erinn P. & Austin, Andrew D., 2020, Synopsis of the parasitoid wasp genus Cotesia Cameron, 1891 (Hymenoptera: Braconidae: Microgastrinae) in Australia, with the description of seven new species, pp. 1-70 in European Journal of Taxonomy 667 (667)</i> on pages 51-52, DOI: 10.5852/ejt.2020.667, <a href="http://zenodo.org/record/3899324">http://zenodo.org/record/3899324</a&gt

    Cotesia flavipes Cameron 1981

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    <i>Cotesia flavipes</i> Cameron, 1981 <p>Figs 6C, 17</p> <p> <i>Cotesia flavipes</i> Cameron, 1891: 185 (holotype, ♂, NHMUK).</p> <p> <i>Apanteles nonagriae</i> Viereck 1913: 645.</p> <p> <i>Apanteles flavipes</i> Wilkinson, 1928a: 93 (synonymy with <i>A. nonagriae</i>), see Shenefelt (1972), Yu <i>et al.</i> (2016) and Fernández-Triana <i>et al.</i> (2020) for extra-limital synonyms and notes.</p> Diagnosis <p> <i>Cotesia flavipes</i> can be separated from nearly all other species of <i>Cotesia</i> currently described from Australia and Papua New Guinea by the dorsoventrally flattened mesosoma, and can be separated from the closely related <i>Cotesia nonagriae</i> (described from Australia, presence in Papua New Guinea unconfirmed) most easily by molecular data (e.g., Genbank: DQ232336 from India, DQ232335 from Pakistan) (Muirhead <i>et al.</i> 2012; also see under <i>C. nonagriae</i>), and also by the shape of the face projection between the antennal bases. When viewed under SEM, the projection is more prominent and rounded with a relatively smooth margin, compared to <i>C. nonagriae</i> which has the margin tri-lobed and the projection less prominent.</p> Material examined <p> <b>Other material</b></p> <p> INDONESIA • 1 ♀; Sumatra, Lapung; 2 Jul. 1982; 4965; ex. L. <i>Chilo sacchariphagus</i> (Bojer, 1856); CIE A14465; WINC.</p> <p> INDIA • 1 ♀; “ H.P. Solan, Deothi”; ex. <i>Chilo partellus</i> (C. Swinhoe, 1885); Sep. 1982; Ram Pratap No.9; CIE A14665; WINC.</p> Distribution <p> <i>Cotesia flavipes</i> is a cosmopolitan species which has been introduced into several countries (e.g., Barbados, Brazil, Colombia, Kenya, Mauritius, Peru, Rèunion, South Africa, USA) for biological control purposes (Muirhead <i>et al.</i> 2006). In the Australasian region it is recorded from Papua New Guinea (Muirhead <i>et al.</i> 2012).</p> Host <p> Known to parasitise many different species of Noctuidae Latreille, 1809 and Crambidae Latreille, 1810; in Papua New Guinea reared from <i>Sesamia grisecens</i> Warren, 1911 (Noctuidae), gregarious (Muirhead <i>et al.</i> 2006).</p> Remarks <p> We include this species in the key due to its presence in Papua New Guinea. Until recently, <i>C. flavipes</i> was recorded as being present in Australia, but the Australian specimens have been identified as <i>C. nonagriae</i>, and this species raised from synonymy (Muirhead <i>et al</i>. 2008). <i>Cotesia flavipes</i> is therefore not currently recorded from Australia, but may possibly be introduced in the future for the control of stem-boring pests.</p>Published as part of <i>Fagan-Jeffries, Erinn P. & Austin, Andrew D., 2020, Synopsis of the parasitoid wasp genus Cotesia Cameron, 1891 (Hymenoptera: Braconidae: Microgastrinae) in Australia, with the description of seven new species, pp. 1-70 in European Journal of Taxonomy 667 (667)</i> on page 23, DOI: 10.5852/ejt.2020.667, <a href="http://zenodo.org/record/3899324">http://zenodo.org/record/3899324</a&gt

    Cotesia medusae Fagan-Jeffries & Austin 2020, sp. nov.

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    <i>Cotesia medusae</i> sp. nov. <p>urn:lsid:zoobank.org:act: DEE8E0E8-BD4D-4780-AAD2-326505BA750A</p> <p>Figs 10C, 11D, 12A, 20</p> Diagnosis <p> <i>Cotesia medusae</i> sp. nov. can be separated from all other species of <i>Cotesia</i> currently described from Australia and Papua New Guinea by the following combination of characters: anteromesoscutum punctate reticulate; antennal flagellomere 14 length/width> 2; scutellar disk smooth with only shallow punctures associated with setae and with centre of medial posterior band of the scutellum smooth; fore wing r vein straight and fore wing 2RS not creating a ‘stub’ at junction with r; T2 semicircle shaped, border with T3 often shallowly crenulate; T3 mostly dark with some pale areas and sparse setae over most of tergite, notauli clearly differentiated from surrounding anteromesoscutum sculpturing.</p> Etymology <p> This species is named after Medusa, the ‘Gorgon’ or monster in Greek mythology. Gorgonphone, the species name of the host (<i>Catopsilia gorgophone</i> Boisduval, 1836) means ‘Gorgon-Slayer’. Thus, there seems to be an appropriate amount of irony in the lethal parasitoid of this species being named for the original monster.</p> Material examined <p> <b>Holotype</b></p> <p> AUSTRALIA • ♀; Queensland, Brisbane; emg. Jun. 2013; R. Kendall leg.; reared from larva of <i>Catopsilia gorgophone</i> (Lepidoptera: Pieridae); BOLD (from co-reared specimen): AUMIC543-19; Genbank <i>COI</i> (from co-reared specimen): MN182699; QM T246704.</p> <p> <b>Paratypes</b></p> <p>AUSTRALIA • 2 ♀♀, 2 ♂♂; same collection data as for holotype; QM T246705-8.</p> Description <p> <b>Female</b></p> <p>COLOUR.Head, antenna and mesosoma dark, dorsal metasoma dark but lighter than mesosoma, darkening posterior to T3, non-sclerotised areas of T1–2 and lateral edges of T3 pale; anterior sternites pale, darkening posteriorly; (fore-, mid-, hind coxa) dark, dark, dark but lighter than fore- and mesocoxa; femora (fore-, mid-, hind femur) pale, pale, pale darkening distally; tibiae (fore-, mid-, hind tibia) pale, pale, light brown darkening distally; tegula and humeral complex dark; pterostigma dark; fore wing veins light brown to dark.</p> <p>BODY LENGTH. Head to apex of metasoma: 2.2 (2.3) mm.</p> <p>HEAD. Antenna slightly longer than body length; OOL/posterior ocellus diameter 2.2; POL/posterior ocellus diameter 1.9 (1.7); antennal flagellomere 2 length/width 2.7 (2.5); antennal flagellomere 14 length/width 1.8 (2.0).</p> <p>MESOSOMA. Anteromesoscutum sculpturing punctate reticulate, transitioning to almost reticulate rugose along lines of notauli; number of pits in scutoscutellar sulcus 8 (9); scutellar disc with only shallow pits associated with setae; maximum height of mesoscutellum lunules/maximum height of lateral face of mesoscutellum 0.7 (0.6).</p> <p>WINGS. Fore wing length 2.3 mm; length of veins r/2RS 1.1 (1.0); length of veins 2RS/2M 1.6 (2.1); length of veins 2M/(RS+M)b 1.0 (0.9); pterostigma length/width 2.7 (2.8).</p> <p>LEGS. Hind tibia inner spur length/metabasitarsus length 0.5.</p> <p>PROPODEUM. Posterolateral thirds smooth, centre third rugose, medial carina only faintly distinct from surrounding rugosity.</p> <p>METASOMA. T1 length /T1 width at posterior margin 1.6; parallel sided, mostly smooth, only small punctures associated with setae; T2 width at posterior margin/T2 length 2.3 (2.2), semicircle shaped, smooth with shallow crenulate border all the way round, T2 length / T3 length 0.6 (0.8); T3 sculpture smooth and shiny; ovipositor sheaths length/hind tibial length 0.07 (0.1).</p> <p> <b>Male</b></p> <p>As female, only slight variations in measurements.</p> Host <p> <i>Catopsilia gorgophone</i> (Pieridae), gregarious.</p> Distribution <p>Currently only known from the type locality in Brisbane, although as the host is found through much of New South Wales and Queensland, this parasitoid also likely has a wider range than currently documented.</p> Remarks <p> Whilst only a 340 bp section of <i>COI</i> was obtained for this species, which is not long enough to be assigned a BIN on BOLD, it is clearly distinct morphologically and genetically from any publically available sequence of <i>Cotesia</i>, and as host data is available we felt the description was warranted despite not possessing a full <i>COI</i> barcode.</p>Published as part of <i>Fagan-Jeffries, Erinn P. & Austin, Andrew D., 2020, Synopsis of the parasitoid wasp genus Cotesia Cameron, 1891 (Hymenoptera: Braconidae: Microgastrinae) in Australia, with the description of seven new species, pp. 1-70 in European Journal of Taxonomy 667 (667)</i> on pages 30-31, DOI: 10.5852/ejt.2020.667, <a href="http://zenodo.org/record/3899324">http://zenodo.org/record/3899324</a&gt

    Cotesia urabae Austin & Allen 1989

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    <i>Cotesia urabae</i> Austin & Allen, 1989 <p>Fig. 31 A–B</p> <p> <i>Cotesia urabae</i> Austin & Allen, 1989: 171 (holotype, ♀, ANIC).</p> <p> <i>Cotesia urabae –</i> Austin & Dangerfield 1992: 22.</p> Diagnosis <p> <i>Cotesia urabae</i> can be separated from all other species of <i>Cotesia</i> currently described from Australia and Papua New Guinea by the following combination of characters: T1 broadening consistently posteriorly, almost wedge shaped; scutellar disk smooth with small punctures associated with setae; mesosoma not dorsoventrally flattened; hind coxa and metasoma as dark; ocelli normal sized, ocular-ocellar line/ posterior ocellus diameter <2.4; fore wing vein r normally longer than, occasionally of similar length to 2RS; hind tibia with only a very small darkened patch, mainly in dorsal view.</p> Material examined <p> <b>Paratype</b></p> <p> AUSTRALIA • ♀; South Australia, Waite Agricultural Research Institute lab colony; Jan. 1986; G.R. Allen leg.; ex. <i>Uraba lugens</i>; WINC.</p> Distribution <p> SA (record from original description), Tas (record from Muirhead <i>et al.</i> 2006; Rowbottom <i>et al.</i> 2013), New Zealand (introduced, see Avila <i>et al.</i> 2015).</p> Host <p> <i>Uraba lugens</i> Walker, 1866 (Noctuidae), solitary (record from original description).</p> Remarks <p>As this species is only recently described and the description is relatively complete, here we provide only new characters or measurements relevant to the diagnosis, and refer otherwise to the description in Austin & Allen (1989).</p>Published as part of <i>Fagan-Jeffries, Erinn P. & Austin, Andrew D., 2020, Synopsis of the parasitoid wasp genus Cotesia Cameron, 1891 (Hymenoptera: Braconidae: Microgastrinae) in Australia, with the description of seven new species, pp. 1-70 in European Journal of Taxonomy 667 (667)</i> on pages 56-58, DOI: 10.5852/ejt.2020.667, <a href="http://zenodo.org/record/3899324">http://zenodo.org/record/3899324</a&gt

    Synopsis of the parasitoid wasp genus Cotesia Cameron, 1891 (Hymenoptera: Braconidae: Microgastrinae) in Australia, with the description of seven new species

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    The genus Cotesia Cameron, 1891 is one of the most diverse of the Microgastrinae, a subfamily of wasps that are exclusively endoparasitic on lepidopteran larvae. Species of Cotesia are widely utilised as biological control agents across the world. In Australia, there are currently 10 confirmed native species as well as four species introduced for the management of lepidopteran pests. The genus is morphologically conserved and has not been studied in the Australasian region for many decades. In this study, we use both comparative morphology and sequence data from the COI gene to delineate species, and in so doing describe seven new species from Australia: C. lasallei sp. nov., C. medusae sp. nov., C. ocellata sp. nov., C. reidarum sp. nov., C. scripta sp. nov., C. tjapekki sp. nov. and C. wonboynensis sp. nov., raising the number of species of Cotesia formally recorded in Australia to 21. We also provide updated descriptions of the previously described native species, diagnoses for the introduced species and a key to all currently described species found on the continent and from Papua New Guinea. This study treats only a fraction of the likely diversity of Cotesia, but provides a solid framework for future work

    Cercobarcon Tobias 1979

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    Genus <i>Cercobarcon</i> Tobias 1979 <p> <i>Type</i></p> <p> <i>Cercobarcon rieki</i>; Tobias, 1979: 75 (by original designation), ANIC (examined).</p> <p> <i>Cercobarcon</i>: van Achterberg, 1984: 52; Naumann, 1991: 946; Austin et al. 1993:113; Quicke et al. 2020: 7.</p> <p> <i>Diagnosis</i></p> <p> Occipital carina well developed; maxillary palps 4-segmented, labial palps 3-segmented; tarsal claws pectinate; fore wing vein 1-SR+M incomplete in basal half, SR1 evenly curved so that marginal cell is acute distally; hind wing vein 1-CU straight; spiracles approximately one-quarter length of propodeal lateral margin or less; in dorsal view metasoma fusiform in shape, terga 2 and 3 not forming a carapace, terga 4 <i>–</i> 6 visible dorsally.</p> <p> <i>Comments</i></p> <p> <i>Cercobarcon</i> can be separated from <i>Trachypetus</i> most easily by the latter having a pedunculate metasoma which forms a carapace, and from <i>Megalohelcon</i> by this genus having an incomplete occipital carina, larger propodeal spiracles (0.35 greater than the medial length of the propodeum), simple claws, and fore wing vein CU-1 curved. The genus is known from five species, including the one described here. It is found broadly across the arid zone from central Queensland to the western margin of the continent, with two species occurring on Cape York Peninsula. The genus is apparently absent from the eastern coastal margin, and temperate/Mediterranean south-east and south-west corners of the continent. However, given that specimens are rarely collected, the distribution of the genus may be broader than is currently documented.</p> <p> <b> Key to species of <i>Cercobarcon</i></b> </p> <p>1. Lower margin of clypeus evenly curved or at most very slightly indented medially (Figure 1 (a))................................................................................................................................................. 2</p> <p>- Lower margin of clypeus deeply sinuate or bilobed (Figure 1 (b,c)).................................... 4</p> <p>2. Fore wing vein 1-SR+M with small terminal swelling (Figure 3 (b,e)); dorsal head, scutum and scutellum dark brown to black.................................................................................................. 3</p> <p> - Fore wing vein 1-SR+M without small terminal swelling (Figure 3 (c,d)); dorsal head, scutum and scutellum red-brown............................................................ <b> <i>C. rieki</i> Tobiası 1979</b> </p> <p> 3. Posterior marginal carina of propodeum slightly sinuate (Figure 4 (b)); metanotum anteromedial area without medial longitudinal carinae, posteromedial area flat (Figure 4 (b)); body all black, except propodeum which is brown-black..................................................................................................... <b> <i>C. niger</i> Austinı Wharton and Dangerfieldı 1993</b> </p> <p> - Posterior marginal carina of propodeum evenly curved (Figure 4 (a)); metanotum anteromedial area foveate, with several medial longitudinal carinae, posteromedial area slightly depressed (Figure 4 (a)); dorsal head, scutum and scutellum dark brown, propodeum red-brown, metasoma dark brown, T1 more red-brown than T2 <i>–</i> T6................................................................................................................................................. C. lasallei <b>sp. nov</b>.</p> <p> 4. Clypeus deeply sinuate (Figure 1 (b)); postscutellar depression evenly crenulated; propodeum rugose-punctate, with irregular slightly coarser carina................................................................................................................... <b> <i>C. grossi</i> Austinı Wharton and Dangerfieldı 1993</b> </p> <p> - Clypeus bilobed (Figure 1 (c)); postscutellar depression with strong medial carina and much fainter lateral crenulae; propodeum with strong medial and lateral carinae, background sculpturing varying from almost smooth to rugose-punctate....................................................................................... <b> <i>C. bilobatus</i> Austinı Wharton and Dangerfieldı 1993</b> </p>Published as part of <i>Austin, Andrew D. & Fagan-Jeffries, Erinn P., 2020, A new species of the enigmatic Australian endemic family Trachypetidae (Hymenoptera: Ichneumonoidea): Cercobarcon lasallei sp. n., pp. 553-563 in Journal of Natural History 54 (9)</i> on pages 554-555, DOI: 10.1080/00222933.2020.1747652, <a href="http://zenodo.org/record/4290256">http://zenodo.org/record/4290256</a&gt
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