Aprionus paludosus Jaschhof & Mamaev, 1997
publication ID |
https://doi.org/ 10.5852/ejt.2017.378 |
publication LSID |
lsid:zoobank.org:pub:81628632-5B35-49E5-AB7A-B8B50B2FB06B |
DOI |
https://doi.org/10.5281/zenodo.6030062 |
persistent identifier |
https://treatment.plazi.org/id/03CF87D4-097C-0447-FE5B-7AEFFABDFC8E |
treatment provided by |
Plazi |
scientific name |
Aprionus paludosus Jaschhof & Mamaev, 1997 |
status |
stat. nov. |
Aprionus paludosus Jaschhof & Mamaev, 1997 View in CoL stat. rev.
Fig. 10 View Fig
Aprionus paludosus is revived here from synonymy with A. styloideus , which reverses our previous decision on the identity of these two species, while the synonymy of Aprionus bicuspidatus Mamaev, 1998 with A. paludosus is confirmed (see Jaschhof & Jaschhof 2009: 243). Our present study revealed A. paludosus to be the most common and most widespread species of the styloideus group.
Diagnosis
The gonostylus ( Fig. 10A View Fig ) is strongly flattened, slightly convex basally, and twice as long as wide, the width being constant from the base to the apex; the basolateral apophysis is of normal size; the large tooth is inserted slightly dorsolaterally rather than right on the apex (↓). The tegmen, which is 2.7 times as long as wide, is broadest below the midlength (↓); the 2–3 pairs of large fingers intersect slightly (↓); the tegminal apex is rounded, seldom more blunt. The anterior corners of the subanal plate have small, dot-like sclerotizations, sometimes surrounded by larger, subrectangular, weakly sclerotized portions (↓). The gonocoxal apodemes are so long that the dorsal bridge, which is narrowly rounded, extends clearly beyond the ventroanterior gonocoxal edge (↓). The postfrons is setose; antennal translucent sensilla are single-pointed; the neck of the fourth flagellomere is shorter than the node ( Fig. 10B View Fig ); the palpus is 4-segmented (if 3-segmented, then the apical segment is clearly the result of two fused segments); and postocular bristles number 9–11.
Material examined
Specimens (incl. types) in DEI listed by Jaschhof (1998), specimens in NHRS listed by Jaschhof & Jaschhof (2009).
SWEDEN: 1 ♂, Skåne, Klippans, Skäralid, Liema, beech forest, MT, SMTP (trap 37, collecting event 831), 20 May–11 Jun. 2004 (no. CEC 328); 1 ♂, Uppland, Uppsala, Fiby NR, 59.72° N, 17.34° E, mixed swampy taiga, MT, MCJ leg., 23 Jun.–28 Jul. 2009 (no. CEC 329); 1 ♂, Uppland, Älvkarleby, Båtfors, 60.27° N, 17.19° E, blueberry-pine forest, MT, SMTP (trap 7, collecting event 378), 17 Jun.–3 Jul. 2003 (no. CEC 330); 1 ♂, Lule Lappmark, Sorsele, Vindelfjällen NR, 6 km W of Ammarnäs, herb-rich subalpine birch forest, MT, MCJ leg., 7 Jul.–12 Aug. 2009 (no. CEC 331).
Distribution and phenology
Norway, Sweden (Skåne, Södermanland, Uppland, Dalarna, Västerbotten, Lule Lappmark, Pite Lappmark, Norrbotten), Finland, Germany (Schleswig-Holstein, Mecklenburg-Vorpommern), European Russia; presumably more widespread, with records in literature (see Jaschhof & Jaschhof 2009, as A. styloideus ) from Denmark, Latvia, Estonia, and the East Palaearctic in need of validation. Adults were collected from May to August in various types of forest, with some preference of swampy sites.
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Phylum |
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Class |
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Order |
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SubOrder |
Bibionomorpha |
Family |
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SubFamily |
Micromyinae |
Genus |