Delia coarctoides Michelsen
publication ID |
https://doi.org/ 10.5281/zenodo.175665 |
DOI |
https://doi.org/10.5281/zenodo.6244319 |
persistent identifier |
https://treatment.plazi.org/id/03D987DE-FF9F-777F-3CAD-FF1FFD28F874 |
treatment provided by |
Plazi |
scientific name |
Delia coarctoides Michelsen |
status |
sp. nov. |
Delia coarctoides Michelsen View in CoL , sp. nov.
Figs. 1 View FIGURES 1 – 2 , 3 View FIGURES 3 – 4 , 5 View FIGURES 5 – 6 , 7–11 View FIGURES 7 – 11 .
Etymology. The specific epithet ‘coarctoides’ is derived from ‘coarctata’, existing name for the most similar species, and ‘oides’, a Greek adjectival suffix meaning ‘resembling’.
Material examined. Type material. Holotype male, DENMARK: Jutland (W): Årgab, reared 16.ix.1951 from puparium found 30.vii.1951 (K.O. Leth), ZMUC. Paratypes. DENMARK: Jutland (W): 5 males, 5 females with same data as for the holotype, ZMUC.
Additional material (in ZMUC if not stated otherwise). CZECH RUPUBLIC: BilinaVršiček, mixed wood, 420m, Malaisetrap, 1 male 25.vi–23.vii.1998 (Barták). DENMARK: W Jutland: Årgab, 29 males, 21 females, reared 16.ix.1951 from puparia found 30.vii.1951 (K.O. Leth); Skallingen, 1 male 10.vii.1932, 1 female 25.vii.1932 (E. Bro Larsen). NE Jutland: Hulsig, 1 male 11.vii.1908 (Mortensen); Skagen, Grenen, 1 male 17.vii.1985 (H. Enghoff). FINLAND: Nylandia: Tvärminne, 2 males 12.viii.1923 (F. Frey), FMNH. Karelia australis: Vehkalahti, 1 male 3.viii.1974 (Tiensuu), FMNH. Tavastia australis: Topeno, Loppi, 1 male 8.vii.2005 (I. Kakko). Karelia borealis: Joensuu, 2 males 913.vii.1976, 1 male 9.viii.1982 (O. Martin). SWE DEN: Skåne: Löderup, 1 male, 1 female 11.vii.1923 (O. Ringdahl); Hagestad, 1 male 11.viii.1983 (H. Andersson), MZLU.
Description. The general descriptions of D. coarctata given by Hennig (1974a) and Griffiths (1991, 1992) also apply to the new species D. coarctoides with a few exceptions as emphasized in the following. It is reliably separated from D. coarctata in the male sex only, although a differential description of both sexes is attempted in the following:
Male. Vein C on basal section, between humeral and subcostal breaks, with several v setulae vs. bare on ventral surface. Fore tibia with apical pv seta short, pointed at tip ( Fig. 1 View FIGURES 1 – 2 ) vs. long and coarse, truncated at tip ( Fig. 2 View FIGURES 1 – 2 ). Length of fore tarsomere 1 equals length of fore tarsomeres 2–4 combined ( Fig. 1 View FIGURES 1 – 2 ) vs. fore tarsomere 1 nearly as long as tarsomeres 2–5 combined ( Fig. 2 View FIGURES 1 – 2 ). Mid tibia with 2 pd and 2 pv setae normally developed vs. same setae strikingly short and weak. Cercal plate in caudal view short, cordiform, less than 1.5 x longer than wide ( Fig. 3 View FIGURES 3 – 4 ) vs. elongated, in caudal view c. 2.0 x longer than wide ( Fig. 4 View FIGURES 3 – 4 ). Surstylus in lateral view markedly expanded on subdistal part ( Fig. 5 View FIGURES 5 – 6 ) vs. barely expanded subdistally ( Fig. 6 View FIGURES 5 – 6 ). Phallus, gonites and hypandrium ( Fig. 7 View FIGURES 7 – 11 ) and sternite V ( Fig. 8 View FIGURES 7 – 11 ) as in D. coarctata .
Female. Prealar seta short but distinct vs. absent or indiscernible from surrounding ground setulae. Vein C on basal section, between humeral and subcostal breaks, with several v setulae vs. bare on ventral surface. Spermathecae and ducts ( Fig. 9 View FIGURES 7 – 11 ) and distal sclerites of oviscapt ( Figs. 10–11 View FIGURES 7 – 11 ) as in D. coarctata .
Taxonomic remarks. I have earlier ( Michelsen 1983, 1985) examined the primary types of Musca coarctata Fallén , Anthomyza leptogaster Zetterstedt and Aricia paralleliventris Zetterstedt and can confirm that they all belong to Delia coarctata (Fallén) . Hennig (1974a) further examined the female holotype of Hylemyia garbiglietti Rondani from Piemonte, Italy and synonymized it with D. coarctata . I cannot see any reason to question Hennig’s identification.
Distribution and biology. Known so far only from a few localities in southern Fennoscandia and a single record from the Czech Republic. The known collecting sites in Denmark and Sweden all have sandy coasts with white dunes or similar sandy, sparsely vegetated areas dominated by marram ( Ammophila arenaria ) and lymegrass ( Leymus arenarius ). A likely possibility is therefore that either of these coarse grasses is favoured as a host plant for the larva of D. coarctoides .
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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