Pristiphora appendiculata (Hartig, 1837)
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https://dx.doi.org/10.3897/jhr.51.9162 |
publication LSID |
lsid:zoobank.org:pub:B3D68EDB-9CF8-44A3-BC43-E9C2D6626BD7 |
persistent identifier |
https://treatment.plazi.org/id/75E6B578-416B-9E6D-A915-F737376DDC65 |
treatment provided by |
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scientific name |
Pristiphora appendiculata (Hartig, 1837) |
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Pristiphora appendiculata (Hartig, 1837)
Pristiphora pallipes Serville, 1823: 75. Secondary homonym of Tenthredo pallipes Fallén, 1808 [= Pristiphora (Lygaeotus) 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 (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; here designated) 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.
Nematus enervis Herrich-Schäffer, 1840: 176. Replacement name for Pristiphora pallipes Lepeletier, 1823.
Nematus cathoraticus Förster, 1854: 325-326. Lectotype ♀ (GBIF-GISHym3214; here designated) 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.
Nematus pallicornis var. labratus Norton, 1861: 160. Holotype ♀ possibly in ANSP or MHNG, not examined. Type locality: Massachusetts, USA. Note. Nematus labratus Norton, 1861 and Nematus pallicornis var. labratus Norton, 1862 ( Norton 1861) were wrongly both listed as available names by Taeger et al. (2010). They refer to the same nominal taxon, described together with N. pallicornis in a single text section by Norton (1861). In the headline to this section, Norton mentions the manuscript names N. pallicornis and N. labratus (nomina nuda) used by Harris (1835). At the end of his description, Norton wrote "A variety named Nematus labratus , by Dr. Harris [...]". The name Nematus labratus was therefore originally published as a variety.
Pristiphora grossulariae Walsh, 1866: 123. Neotype ♀ (selected by Zinovjev and Smith 2000) in ANSP, not examined. Type locality: possibly (if the neotype belongs to syntype series) Davenport, Iowa, USA.
Nematus Peletieri [sic!] André, 1880: 111. Name for Pristiphora pallipes Lepeletier, 1823.
Nematus hypobalius Zaddach in Brischke, 1884: 154. Holotype ♀ possibly destroyed ( Blank and Taeger 1998). Type locality: Hungary.
Nematus pumilus Zaddach in Brischke, 1884: 172. 2 ♂ syntypes possibly destroyed ( Blank and Taeger 1998). Type locality: Chernyakhovsk [Insterburg], Kaliningrad Oblast, Russia.
Nematus Ghilianii [sic!] Costa, 1894: 73. Syntype(s) ♂ possibly in MZUN, not examined. Type locality: Alps [Alpi boreali], Europe.
Similar species.
Smooth mesopostnotum (Fig. 7 View Figures 3–17 ) and claws without subapical tooth (Fig. 30 View Figures 18–36 ) allow unambiguous distinction of this species from other European species of the Pristiphora ruficornis group. A specimen from China (DEI-GISHym17879) that can be identified as P. ribisi Togashi, 1990 (described from Japan), is externally not distinguishable from P. appendiculata , but has a distinctly different saw (Fig. 39 View Figures 37–40 ) by having well developed ctenidia and serrulae with numerous denticles on the ventro-apical surface (ctenidia are practically absent and serrulae are almost without denticles on the ventro-apical surface in P. appendiculata ; Figs 37-38 View Figures 37–40 ).
Genetic data.
Based on COI barcode sequences, specimens of this species are divided between two BIN clusters (BOLD:AAG7866 and BOLD:AAU8684). Minimum distance between the clusters is 3.26%. However, one of the BINs might represent a cluster of nuclear mitochondrial pseudogenes (NUMTs). The COI sequence (1078 bp) we obtained from the specimen DEI-GISHym21073 was different (belonging to BOLD:AAG7866) from the one present in BOLD (BASYM3303-14, 652 bp; belonging to BOLD:AAU8684) (Fig. 1 View Figure 1 ). Our use of different primers (see Material and methods) from those used by the Canadian Centre for DNA Barcoding might explain the result. Because the sequences under BOLD:AAU8684 (all 8 sequences in BOLD are identical) have an unusual 6-nucleotide deletion and this BIN forms a distinctly longer branch (which means more mutations) in the phylogenetic tree (Fig. 1) than other sequences in the Pristiphora appendiculata subgroup, it might represent the NUMT cluster rather than BOLD:AAG7866. Alternatively, specimen DEI-GISHym21073 might be heteroplasmic for mitochondrial DNA (different mitochondria co-existing in the same cell or individual). Because sequences from both of these BINs can apparently be present in the same individual, these BINs seem to form a monophyletic group (Fig. 1 View Figure 1 ), and because there appear to be no morphological characters that distinguish these BIN clusters, we treat them as one species. Closest to these BIN clusters is a specimen from China that we identified as P. ribisi (Fig. 1 View Figure 1 ). Amplification of nuclear TPI sequences was unfortunately unsuccessful.
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, and Sweden.
No known copyright restrictions apply. See Agosti, D., Egloff, W., 2009. Taxonomic information exchange and copyright: the Plazi approach. BMC Research Notes 2009, 2:53 for further explanation.
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Pristiphora appendiculata (Hartig, 1837)
Prous, Marko, Vikberg, Veli, Liston, Andrew & Kramp, Katja 2016 |
Nematus hypobalius
Zaddach 1884 |
Nematus pumilus
Zaddach 1884 |
Nematus pallicornis
Norton 1861 |
Nematus cathoraticus
Forster 1854 |
Pristiphora (Lygaeotus) carinata
Hartig 1837 |
Nematus appendiculatus
T.Hartig 1837 |
Nematus fuscicornis
Hartig 1837 |
Tenthredo (Nematus) pallicornis
Fabricius 1798 |