Pristiphora appendiculata (Hartig, 1837)

Prous, Marko, Kramp, Katja & Liston 1, Veli VikbergAndrew, 2017, North-Western Palaearctic species of Pristiphora (Hymenoptera, Tenthredinidae), Journal of Hymenoptera Research 59, pp. 1-190 : 62

publication ID

https://dx.doi.org/10.3897/jhr.59.12565

publication LSID

lsid:zoobank.org:pub:598C5BB3-2136-4D91-B522-FA14D8874A52

persistent identifier

https://treatment.plazi.org/id/226AC805-AF0B-00A3-5514-CD9398689852

treatment provided by

Journal of Hymenoptera Research by Pensoft

scientific name

Pristiphora appendiculata (Hartig, 1837)
status

 

Pristiphora appendiculata (Hartig, 1837) Figs 19, 21, 61, 105, 187, 262

Pristiphora pallipes Serville, 1823: 75. Secondary homonym of Tenthredo pallipes Fallén, 1808 [= Pristiphora carinata (Hartig, 1837)]. Lectotype ♀ (designated by Lacourt 2000) in MNHN, not examined. Type locality: Paris, France.

Pristiphora pallipes Lepeletier, 1823: 60. Primary homonym of Pristiphora pallipes Serville, 1823 [= Pristiphora appendiculata (Hartig, 1837)]. Lectotype ♀ (designated by Lacourt 2000) in MNHN, not examined. Type locality: Paris, France.

Tenthredo (Nematus) pallicornis T.W. Harris, 1835: 583. Type(s) not available. Nomen nudum.

Tenthredo (Nematus) labrata T.W. Harris, 1835: 583. Type(s) not available. Nomen nudum.

Nematus flavipes Dahlbom, 1835a: 25-26. Nomen oblitum. Holotype ♀ in MZLU, examined. Type locality: Lund, Sweden.

Nematus appendiculatus Hartig, 1837: 202-203. Nomen protectum. See Blank et al. (2009). Lectotype ♀ (GBIF-GISHym3197; designated by Prous et al. 2016) in ZSM, examined. Type locality: Germany according to the title of the publication.

Nematus fuscicornis Hartig, 1837: 225. No syntypes were found in ZSM. Type locality: Harz, Germany. Synonymised with Nematus appendiculatus by Stein (1881).

Nematus enervis Herrich-Schäffer, 1840: 176. Replacement name for Pristiphora pallipes Lepeletier, 1823.

Nematus cathoraticus Förster, 1854: 325-326. Lectotype ♀ (GBIF-GISHym3214; designated by Prous et al. 2016) in ZSM, examined. Type locality: Aachen, North Rhine-Westphalia, Germany.

Nematus pallicornis Norton, 1861: 160. 3 ♀ syntypes in MCZ (http://140.247.119.225/mcz/Species_record.php?id=22468), although 4 specimens were mentioned in the original description, not examined. Type locality: Massachusetts, USA. Synonymised with P. pallipes by Smith (1966).

Nematus pallicornis var. labratus Norton, 1861: 160. Holotype ♀ possibly in ANSP or MCZ. Type locality: Massachusetts, USA. Synonymised with P. rufipes auct. by Smith (1979).

Pristiphora grossulariae Walsh, 1866: 123. Neotype ♀ (designated by Zinovjev and Smith 2000) in ANSP, not examined. Type locality: possibly (if the neotype belongs to the syntype series) Davenport, Iowa, USA. Synonymised with Nematus appendiculatus by Dalla Torre (1894).

Nematus Peletieri [sic!] André, 1880: 111. Replacement name for Pristiphora pallipes Lepeletier, 1823.

Nematus hypobalius Zaddach in Brischke, 1884: 154. Holotype ♀ possibly destroyed ( Blank and Taeger 1998). Type locality: Hungary. Synonymised with P. pallipes by Konow (1905).

Nematus pumilus Zaddach in Brischke, 1884: 172. 2 ♂ syntypes possibly destroyed ( Blank and Taeger 1998). Type locality: Chernyakhovsk [Insterburg], Kaliningrad Oblast, Russia. Synonymised with P. pallipes by Konow (1905).

Nematus Ghilianii [sic!] Costa, 1894: 73. Syntype(s) ♂ possibly in MZUN, not examined. Type locality: Alps [Alpi boreali], Europe. Synonymised with P. pallipes by Konow (1905).

Pristiphora (Pristiphora) anivskiensis Haris, 2006a: 194-195, syn. n. Holotype ♂ (DEI-GISHym80340; http://dx.doi.org/10.6084/m9.figshare.5100763) in HNHM, examined. Type locality: Novo-Aleksandrovsk, Sakhalin Oblast, Russia.

Similar species.

Smooth mesopostnotum (Fig. 19), claws without subapical tooth (Fig. 21), and the structure of serrula (Fig. 187) or penis valves (Fig. 262) allow separation of this species from other similar species in the ruficornis and rufipes groups.

Genetic data.

Based on COI barcode sequences, specimens of this species are divided between two BIN clusters (BOLD:AAG7866 and BOLD:AAU8684) (Fig. 1 in Prous et al. 2016). Minimum distance between the clusters is 3.26%. However, BOLD:AAU8684 might represent a cluster of nuclear mitochondrial pseudogenes ( Prous et al. 2016). Based on nuclear data (two specimens and both genes combined), maximum within species divergence is 0.3% and the nearest neighbour is 1.8% different ( P. pusilla ).

Host plants.

Ribes spp. Ribes alpinum L. ( Kangas 1985, as P. rufipes ), R. rubrum L. ( Adam 1973, as P. pallipes ), R. uva-crispa L. emend. Lam. ( Adam 1973, Kangas 1985), R. aureum Pursh ( Adam 1973), R. sanguineum Pursh ( Adam 1973), R. nigrum L. ( Adam 1973), R. spicatum Robs. ( Kontuniemi 1975, as P. pallipes ).

Distribution and material examined.

Palaearctic, Nearctic. Specimens studied are from Austria, Canada, Estonia, Finland, Germany, Russia (Republic of Bashkortostan, Sakhalin Oblast), and Sweden.