Sapromyzosoma quadripunctata (Linnaeus 1758)
publication ID |
https://doi.org/ 10.11646/zootaxa.3780.3.1 |
publication LSID |
lsid:zoobank.org:pub:170F4E3F-847E-48F7-AF68-AA0E4BC7936A |
DOI |
https://doi.org/10.5281/zenodo.6131208 |
persistent identifier |
https://treatment.plazi.org/id/501F0803-ED22-2E15-FF53-FA3FFDA62505 |
treatment provided by |
Plazi |
scientific name |
Sapromyzosoma quadripunctata (Linnaeus 1758) |
status |
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Sapromyzosoma quadripunctata (Linnaeus 1758) View in CoL
The mature larvae relatively large, soft and dorsoventrally flattened, welts and crevices well developed. The Malpighian tubules slightly and irregularly inflated.
Egg. Length 0.67– 0.19 mm. The ridges and ribs well developed, sharp-edged, ribs creating small regular rectangles. Posterior pole with conspicuous tubercle with few openings. Small eggs with ribs only indicated, ridges simple, seldom fusing, the surface tuberculous.
First instar ( Figs 156, 157 View FIGURES 156 – 161 ). Length 1.21–1.45 mm. The facial mask broad, number of scraping cirri per row large (up to 60). The peristomal cirri filiform, aligned in a diagonal row. The labial lobe small (shorter than long). The ventral organ with small basal lobe and two digitiform processes.
Cephaloskeleton. Length 0.25–0.26 mm, very similar to the previous species.
Second instar ( Figs 158–161 View FIGURES 156 – 161 ). Length 2.12–2.85 mm. Facial mask broad, with numerous cirri. First thoracic segment smooth; second one with narrow string of comb spines anterodorsally; third one with broad band of comb spines and hairs. Abdominal segments and anal division dorsally covered by robust spines, laterally by hairs and ventrally by spines on creeping welts.
Cephaloskeleton. Length 0.49–0.51 mm. Very similar to previous species. Potential differences include the shape of subhypostomal sclerites.
Third instar was not obtained.
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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