Naineris australis Hartman, 1957
publication ID |
https://doi.org/ 10.11646/zootaxa.5492.3.6 |
publication LSID |
lsid:zoobank.org:pub:DD79929A-C343-467F-A3AB-31FC7E59705C |
DOI |
https://doi.org/10.5281/zenodo.13286448 |
persistent identifier |
https://treatment.plazi.org/id/41151731-FF86-4F42-FF12-E44883C887A9 |
treatment provided by |
Plazi |
scientific name |
Naineris australis Hartman, 1957 |
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Naineris australis Hartman, 1957 View in CoL
( Fig. 4 View FIGURE 4 )
Naineris grubei australis Hartman, 1957: 303–304 View in CoL , pl. 39, figs 1–4; 1959: 366.— Day 1977: 238.— Hutchings & Rainer 1979: 761.— Hutchings & Murray 1984: 53.— Zhadan et al. 2015: 793–797, figs 10A–G, 11A–C, 12D.
Naineris grubei View in CoL .— Day 1977: 237–238.
Naineris australis View in CoL .— Blake 2017: 103; Zhadan 2020: 479–480 View Cited Treatment , fig. 15A–E (in part).
Material examined. Australia, Queensland: off Casuarina Beach, Lizard Island, coll. K. Meissner and T. Alvestad, 14Aug 2013, 1 m, fine sand, 14.67944°S, 145.44703°E, intertidal, (1, AM W.44038); Heron Island, coll. G. Hartmann-Schröder, coral sand from residual ponds between coral colonies at the North Reef, probably intertidal, 02 Apr 1976 (1, ZMH P-21075). New South Wales: Broughton Island, coll. NSW Fisheries, 01 Sep 1976, Posidonia diving cores, 32.62°S, 152.32°E, intertidal, (1, AM W.13138); Botany Bay, Towra Point, coll. K. Robinson, Jul 1981, Zostera , sand/mud sediment, 34°S, 151.16°E, intertidal, (2, AM W.195061). South Australia: Port Noarlunga, Onkaparinga, Adelaide, Sta. 104a, coll. S. J. Edmonds, 35.150004°S, 138.466649 °E, intertidal, holotype of Naineris australis ( LACM-AHF Poly 676). Western Australia: Exmouth, Town Beach, coll. G. Hartmann-Schröder, 10 Oct 1975, ripple-marked flat, fine silt with little sand, probably intertidal, (5, ZMH P-16592).
Measurements. Holotype 48 mm long, 1.5 mm wide, for 173 chaetigers.
Diagnosis. Spatulate prostomium. Multiple dorsal sensory organs small, oval-shaped, 2–10 per side, grouped in a single longitudinal row throughout body; first segments a pair per side, increasing in number posteriorly, up to ten in abdominal segments, not crossing midline. Thoracic notopodial lobes digitiform. Thoracic neuropodial lobe with an upper tongue-like papilla. Thoracic neurochaetae with 5–6 transverse, posterior rows of numerous subuluncini; a transverse, anterior row of about 20 crenulate capillaries; an inferior, anterior, oblique row of about 20 hooded uncini and an inferior, posterior, oblique row of capillaries.
Redescription. Holotype medium-sized specimen. Color in alcohol pale yellow. Body long, with thorax and abdomen about the same width ( Fig. 4A View FIGURE 4 ). Ventrally thorax smooth, but abdomen, tri-annulate with central ring wider than others.
Prostomium spatulate ( Fig. 4B View FIGURE 4 ); eyespots absent; nuchal organs present at posterior end of prostomium and anterior end of peristomium ( Fig. 4B View FIGURE 4 ). Peristomium with two achaetous rings, weakly delimited. Mouth opening with lips striated; proboscis only partially everted, represented by a lobe ( Fig. 4B View FIGURE 4 ).
Branchiae from chaetiger 6 onwards; long, glandular, and ciliated ( Fig. 4C, D View FIGURE 4 ); first digitiform, half size of abdominal branchiae, then increasing in size and a triangular shape. Abdominal branchiae longer, crossing midline, not reaching opposite branchial base. Multiple dorsal sensory organs per segment present from mid-thoracic chaetigers; small, oval-shaped, 2–10 per side, grouped in single longitudinal row throughout body; first segments one pair per side, increasing in number posteriorly, up to ten in abdominal segments ( Fig. 4F View FIGURE 4 ), not crossing midline. Dorsal crest straight, consistent, flat, forming a low curve ( Fig. 4C, D View FIGURE 4 ).
Thorax weakly depressed, with 38 chaetigers (~4 transitional segments with intermediate characteristics between thoracic and abdominal segments) ( Fig. 4A View FIGURE 4 ). Parapodia biramous. Thoracic notopodial lobes digitiform ( Fig. 4B, C View FIGURE 4 ). Thoracic neuropodial lobes represented by a flange with a tongue-like papillae on superior tip ( Fig. 4B, C View FIGURE 4 ). Abdominal notopodial lobes cirriform ( Fig. 4D, G View FIGURE 4 ). Abdominal neuropodial lobes triangular with a thin projection on tips ( Fig. 4D, G View FIGURE 4 ).
Thoracic notochaetae: 20–30 crenulate capillaries in two bundles.Abdominal notochaetae: two groups of 10–20 crenulate capillaries. Thoracic neurochaetae: a transverse, anterior row of small capillaries, six transverse, posterior rows of numerous subuluncini; an inferior, posterior, oblique row of about 20 crenulate capillaries and an inferior, anterior, oblique row of about 20 hooded uncini ( Fig. 4E View FIGURE 4 ). Abdominal neurochaetae: 3 acicular spines and 5–10 crenulate capillaries.
Pygidium unknown.
Variation: The number of thoracic chaetigers of the specimens studied ranged between 36–50, as in other species it is size-related. Dorsal sensory organs ranged from two to five pairs on posterior segments.
Remarks: Naineris australis was originally described as a subspecies of Naineris grubei ( Gravier, 1908) by Hartman (1957), redescribed by Zhadan et al. (2015) and was elevated to species rank by Blake (2017), based on differences in the structure of the thoracic neurochaetae and the presence of subuluncini in N. australis .
Dorsal sensory organs were not described for N. australis by Hartman (1957), but Zhadan et al. (2015), noted the presence of up to five pairs per segment in specimens from Lizard Island. After examining the holotype and other collections, we observed that they varied throughout the body. We stress that it is difficult to see multiple dorsal organs in preserved specimens, and they are usually visible as small transparent scars. It is necessary to use an appropriate light and contrast medium to facilitate its observation; explaining why often overlooked.
We examined some of the specimens examined by Zhadan (2020), and the voucher AM W.22470 (Fig. 15D, E) was misidentified, corresponding to a specimen of the N. setosa ( Verril, 1900) species complex, bearing only capillaries in thoracic neuropodia, and paired dorsal organs.
Distribution. Southwest Australian Shelf, Southeast Australian Shelf, East-Central Australian Shelf, and Northeast Australian Shelf provinces, intertidal.
T |
Tavera, Department of Geology and Geophysics |
AM |
Australian Museum |
ZMH |
Zoologisches Museum Hamburg |
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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Naineris australis Hartman, 1957
Álvarez, Ricardo & Haggin, Brent M. 2024 |
Naineris grubei
Day, J. H. 1977: 237 |
Naineris grubei australis
Zhadan, A. & Stupnikova, A. & Neretina, T. 2015: 793 |
Hutchings, P. A. & Murray, A. 1984: 53 |
Hutchings, P. & Rainer, S. 1979: 761 |
Day, J. H. 1977: 238 |
Hartman, O. 1957: 304 |