Pherusa sibogae ( Caullery, 1944 ) Salazar-Vallejo, 2014
publication ID |
https://doi.org/ 10.11646/zootaxa.3886.1.1 |
publication LSID |
lsid:zoobank.org:pub:6ADD860C-D60C-448D-BC11-19EDB74013EE |
DOI |
https://doi.org/10.5281/zenodo.4952644 |
persistent identifier |
https://treatment.plazi.org/id/7A4987D3-3265-FFBF-FF37-FB002B02FEF7 |
treatment provided by |
Felipe |
scientific name |
Pherusa sibogae ( Caullery, 1944 ) |
status |
comb. nov. |
Pherusa sibogae ( Caullery, 1944) View in CoL n. comb.
Figure 14 View FIGURE 14
Trophoniella sibogae Caullery, 1944:36–38 View in CoL , Fig. 28.— Bleeker & van der Spoel, 1992:163.
Type material. Eastern Indian Ocean. Holotype ( ZMA 1599 ), off Western Timor, R.V. Siboga, Stat. 299 (10°52'04" S, 124°01'01" E), 34 m. GoogleMaps
Description. Holotype (ZMA 1599) pale, damaged, several parapodia previously removed; anterior and posterior ends better preserved, median region collapsed, narrower than body ends; body cylindrical, slightly tapered posteriorly; 25 mm long, 2 mm wide (chaetiger 7 before constricted region), cephalic cage 4 mm long, 27 chaetigers. Body scarcely papillated; tunic with sediment particles adhered dorsally ( Fig. 14A View FIGURE 14 ) and ventrally ( Fig. 14B View FIGURE 14 ), giving a rough appearance; papillae elongate capitate, apparently arranged in longitudinal series along the body, one row per segment, 3 papillae dorsally, 2 ventrally; largest ones associated with parapodia.
Cephalic hood exposed, short, margin crenulated. Anterior end unknown; not dissected to avoid further damage. Cephalic cage chaetae as long as 1/6 body length, or twice as long as body width. Chaetigers 1–2 forming cephalic cage; chaetae arranged as two lateral series; chaetiger 1 with 8 noto- and 7 neurochaetae, chaetiger 2 with 9 notochaetae and 6 thicker neurochaetae.
Anterior dorsal margin of first chaetiger with rounded anterior projection with small marginal papillae. Chaetigers 1–3 of about the same length. Chaetal transition from cephalic cage to body chaetae abrupt; aristate neurohooks start in chaetiger 4. Gonopodial lobes not seen, probably eroded ( Fig. 14B View FIGURE 14 ).
Parapodia poorly developed; chaetae emerge from body wall. Parapodia lateral; median neuropodia ventrolateral. Notopodia and neuropodia low lobes; chaetal lobes with postchaetal capitate papillae; notopodial papillae very long (at least 5x longer than ventral one). Noto- and neuropodia close to each other.
Median notochaetae arranged in short transverse series; all notochaetae multiarticulated capillaries, articles short basally and medially, distally slightly longer, continued almost to the tip ( Fig. 14D View FIGURE 14 ), 7–8 per fascile (chaetiger 6), as long as 2/3 body width. Neurochaetae multiarticulated capillaries in chaetigers 1–3; aristate neurohooks from chaetiger 4, arranged in transverse series, 4–5 per bundle; anterior neurospines thicker, with aristae broken ( Fig. 14E View FIGURE 14 ), posterior neurospines thinner, aristae delicate, bent ( Fig. 14F View FIGURE 14 ).
Posterior region tapered ( Fig. 14C View FIGURE 14 ); pygidium unknown.
Remarks. Pherusa sibogae ( Caullery, 1944) n. comb., as indicated above, resembles P. rullieri because both have cephalic cages twice as long as body width and aristate neurohooks along the body. These two species differ by the abundance of body papillae and their sediment cover; in P. sibogae body papillae are scarce and there are sand particles over papillae and tunic, whereas in P. rullieri body papillae are abundant, and they do not include sand particles.
Trophoniella Hartman, 1959 has been revised elsewhere ( Salazar-Vallejo 2012b), and it includes species provided with a thick tunic, abundant branchial filaments in a tongue-shaped branchial plate, and with anchylosed neurohooks, at least in posterior chaetigers. Caullery (1944) included three species for Trophoniella and T. sibogae was the only one provided with aristate neurohooks. This species was regarded as belonging to Brada as part of the above generic revision ( Salazar-Vallejo 2012b:459) but that idea was modified once some species of Pherusa were found with aristate neurohooks. Consequently, T. intoshi is transferred to Pherusa and hence the new combination.
Distribution. Only known from the type locality, off Western Timor, in 34 m depth.
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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Pherusa sibogae ( Caullery, 1944 )
Salazar-Vallejo, Sergio I. 2014 |
Trophoniella sibogae
Bleeker, J. & van der Spoel, S. 1992: 163 |
Caullery, M. 1944: 38 |