Dacrysoma imitatum, Darby, Michael, 2013
publication ID |
https://doi.org/ 10.11646/zootaxa.3718.3.2 |
publication LSID |
lsid:zoobank.org:pub:003A16B5-34C5-48F8-A41C-8B784F3B06CB |
DOI |
https://doi.org/10.5281/zenodo.6154613 |
persistent identifier |
https://treatment.plazi.org/id/E4DEAB6A-689E-444F-98EE-CD7B7C7BED55 |
taxon LSID |
lsid:zoobank.org:act:E4DEAB6A-689E-444F-98EE-CD7B7C7BED55 |
treatment provided by |
Plazi |
scientific name |
Dacrysoma imitatum |
status |
sp. nov. |
Dacrysoma imitatum View in CoL sp. n.
(Figs.16, 49, 70, 88, 97)
Habitus Fig. 16. Length. 0.80–0.81 mm. Colour: dusky yellow, pronotum slightly darker than elytra, antennae and legs paler yellow. Antennomeres 3–11 Fig. 49 View FIGURES 41 – 55 . Pronotum 0.22 mm long, 0.28 mm wide, Fig. 70 View FIGURES 62 – 76 , +/- 8 punctures between anterior and posterior margins. Elytra: 0.49 mm long, 0.48 mm wide, more finely punctured than pronotum.
Male: aedeagus Fig. 97.
Female: spermatheca Fig. 88 View FIGURES 77 – 89 .
Etymology. This epithet is based on the Latin participle imitatus, meaning imitated, and refers to its morphological similarity with sibling species.
Remarks. Difficult to distinquish on external features so that a dissection of the genitalia is required. The spermatheca could be confused with D. fabrum but is rounder and lacks the distinctive pear shape of that species.
Type data. Holotype: ♂, Ranomafana N.P., sifting, S.21˚14’51’’ E. 47˚24’13’’, 1079 m, 16–18.xi.2010, P. Banar (BMNH). Paratypes: 35 exs, same data as holotype; 2 ♀, Ambohitantely N.P., ABT/ Nov/2011/04, sifting forest litter under palm tree and big rotten trunk, Winkler app. extr., S. 18o11’56.5’’ E.47o17’26.1’’, 1561 m, 17.xi.2011, L.S.Rahanitriniaina (BMNH); 2 exs, Ankarafantsika N.P., AKF/05/2011, sifting forest litter, Winkler app. extr., 89 m, 23.iv.2011, L.S.Rahanitriniaina & R. Raveloson (BMNH).
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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