Dendronereis chipolini, Hsueh, 2019
publication ID |
https://doi.org/ 10.11646/zootaxa.4652.3.10 |
publication LSID |
lsid:zoobank.org:pub:8C09A71C-8E90-4DE4-8AF6-51E16A729B90 |
persistent identifier |
https://treatment.plazi.org/id/6D1D8A77-EA58-D87E-FF33-FA92FDF9FDE2 |
treatment provided by |
Plazi |
scientific name |
Dendronereis chipolini |
status |
sp. nov. |
Dendronereis chipolini View in CoL n. sp.
Figs 1 View FIGURE 1 A–C, 2A–E, 3A–L, 4A–H, Table 1 View TABLE 1
Material examined. Holotype ( NMNS 7861-001 View Materials ), brackish aquaculture ponds nearby the mouth of Kaoping River (22°28.72´N 120°25.93´E), sandy mud bottom, 28 October 1994 GoogleMaps ; 19 paratypes. Eighteen ones ( NMNS 7861-002 View Materials – 019 View Materials ), collection, location, habitat and date information are the same as holotype ; one paratype ( NMNS 7861-020 View Materials ), Chigu (23°3.42´N 120°3.62´E), sandy mud bottom, 6 May 2009. GoogleMaps
Diagnosis. Dendronereis with pharynx with solitary papillae on oral ring only; seven to eight pairs of branchiae, 8 th pair of branchiae if present, minute, with branchial filaments arising from edges of slightly enlarged notopodial dorsal cirrophores; neuropodia of anterior chaetigers with short blunt-tipped blades homogomph spinigers in upper and lower fascicle.
Description. Holotype ( NMNS 7861-001), complete, 105 mm long (48 and 62, from two other complete specimens; paratypes ( NMNS 7861-004, 008)), with 145 (115 and 147) chaetigers, maximum width 3.0 mm at chaetiger 10, excluding parapodia; light brown in alcohol ( Fig. 1A View FIGURE 1 ). Prostomium bent dorsally, wider than long, frontal margin with shallow cleft, with narrow longitudinal grove extending to middle of prostomium; one pair of antennae arising anteriorly; palps with palpophores conical, slightly longer than wide, tapered palpostyles digitate, blunt, barely exposed. Two pairs of blackish, reniform or semilunar, similar sized eyes, with lenses, trapezoid arranged. Peristomium distorted by pharynx eversion, twice wider than long, four pairs of tentacular cirri with distinct cir- rophores, longest posterior tentacular cirri extended to chaetiger 9 (6–9, in paratypes NMNS 7861-002–4, 006, 008) ( Fig. 1B View FIGURE 1 ). Pharynx with one pair of translucent, light brown jaws, each with 9–10 lateral teeth right and left, respectively (9–10 in paratypes ( NMNS 7861-002–4, 009, 014, 017, 019)); paragnaths absent; papillae large, uniseriate, digitate to hemispherical, present only on oral ring ( Fig. 1B, C View FIGURE 1 ), numbers of papillae at each area as: Area V = 0 (0, from paratypes ( NMNS 7861-002–4, 009, 014, 017, 019)); Area VI = 1, 1 (1, 1, from paratypes ( NMNS 7861- 002–4, 009, 014, 017, 019)); Area VII/VIII = 5 (2–6, from paratypes ( NMNS 7861-002–4, 009, 014, 017, 019)) in one transverse row.
Chaetigers 1 and 2 with neuroaciculae only; noto-aciculae present from chaetiger 3 ( Fig. 3 View FIGURE 3 A–D). Dorsal cirri attached basally to notopodial dorsal ligules, with cirrophores; dorsal cirri longer than dorsal ligules on anterior chaetigers ( Fig. 3 View FIGURE 3 A–H), thereafter gradually reducing size, markedly shorter than dorsal ligules in first to third branchial segments, becoming small and forming tips of branchiae in fourth to seventh branchial segments ( Figs 2 View FIGURE 2 B–D, 3I, J), remaining small to posterior end segments; notopodial dorsal cirrophores round, short on chaetigers 1 and 2 ( Fig. 3 View FIGURE 3 A–D), gradually enlarged and depressed along chaetigers 3 to 21 (20 for individuals with seven pairs of branchiae) ( Fig. 2 View FIGURE 2 B–D), thereafter abruptly reduced in size, small to posterior end segments. Both notopodial dorsal and medium ligules progressively longer from chaetiger 1 to 17 ( Figs 2B, C View FIGURE 2 , 3 View FIGURE 3 A–D), markedly reduced in length from chaetigers 18–20, thereafter remaining short ( Figs 2E View FIGURE 2 , 3 View FIGURE 3 K–L). Notopodial prechaetal lobe present from chaetigers 3 to 13, round ( Fig. 3E, G View FIGURE 3 ). Neuropodia of chaetiger 1 with one prechaetal lobe and three (2 for paratype ( NMNS 7861-002)) uneven sized postchaetal lobes ( Fig. 3A, B View FIGURE 3 ), chaetiger 2 with one prechaetal lobe and four (3 for para- type ( NMNS 7861-002)) uneven sized postchaetal lobes ( Fig. 3C, D View FIGURE 3 ), chaetiger 3 to 9 with two prechaetal lobes and five to six subequal postchaetal lobes (four for paratype ( NMNS 7861-002), mostly five for other paratypes) ( Fig. 3E, F View FIGURE 3 ), chaetiger 10 to 14 with two prechaetal lobes and seven subequal postchaetal lobes, chaetiger 15 to 17 with one prechaetal lobe and no postchaetal lobe ( Figs 2B, C View FIGURE 2 , 3I, J View FIGURE 3 ), chaetiger 18 to posterior end without prechaetal lobe and with one postchaetal lobe ( Figs 2D, E View FIGURE 2 , 3 View FIGURE 3 K–L). Ventral cirri attached to base of neuropodia, small throughout.
Notochaetae present from chaetiger 3 to posterior end, all homogomph spinigers with serrated blades; most notochaetae embedded in body flesh with tips of few notochaetae exposed in anterior chaetigers, all notochaetae exposed in subsequent chaetigers ( Fig. 4A, B View FIGURE 4 ). Neurochaetae present from chaetiger 1 to posterior end; chaetigers 1 and 2 with homogomph spinigers, serrated blade medium-sized ( Fig. 4C View FIGURE 4 ), chaetigers 3 to 12 with serrated short to long homogomph spinigers in upper and lower neuropodial fascicles ( Fig. 4D, E View FIGURE 4 ), short blade homogomph spinigers blunt-tipped ( Fig. 4E View FIGURE 4 ); thereafter chaetigers with only long homogomph spinigers with serrated blade.
Branchiae bipinnate, depressed, conical present along chaetigers 15 to 22 (15 to 21 if only seven pairs of branchiae present) ( Figs 1A View FIGURE 1 , 2A View FIGURE 2 ); first to third branchial pairs with conical to clavate lateral lobes arising from enlarged, depressed notopodial dorsal cirrophores, lateral lobes progressively smaller distally ( Fig. 2B, C View FIGURE 2 ); numbers of lobes on each branchia as: first pair=0/7 (left inner/outer edges, respectively) (0/6, from paratype MNMS 7861-002) and 0/6 (right inner/outer edges, respectively) (0/5, from paratype MNMS 7861-002); second pair=0/10 and 5/9 (0/10 and 0/10); third pair=7/8 and 7/ 9 (8/10 and 9/12) ( Fig. 2C View FIGURE 2 ); fourth to seventh pairs with lateral lobes larger, fully developed, arising from notopodial base, with main stem and bipinnate branchial filaments, each filament with many double-rows of smaller filaments; numbers of branchial filaments on each branchia as: fourth pair=15/17 (13/14) (left pinnate) and 14/15 (13/16) (right pinnate); fifth pair=14/15 and 14/17 (20/22 and 15/17); sixth pair=15/16 and 15/18 (15/16 and 16/17); seventh pair=14/17 and 14/15 (11/11 and 11/12) ( Fig. 2D View FIGURE 2 ), eighth pair=2/2 and 1/2 (2/ 3 and 2/4) ( Fig. 2E View FIGURE 2 ) (Variations on numbers of branchial pairs and branchial clavate lobes and filaments see Table 1 View TABLE 1 ).
Pygidium round, anus with multiple incisions ( Fig. 4F View FIGURE 4 ); one pair of anal cirri, attached ventrally, elongate, tapered, reaches 11 th chaetiger from posterior end.
Etymology. The species is dedicated to the memory of Mr. Chi Po-Lin (27 December 1964 – 10 June 2017) aerial photographer and documentary film director who made an immense contribution to environmental protection in Taiwan.
Type locality. Brackish aquaculture ponds nearby the mouth of Kaoping River, Kaohsiung, Taiwan .
Distribution. Only known from the type locality and brackish aquaculture ponds adjacent to the Chigu lagoon, Tainan, Taiwan.
Remarks. Dendronereis chipolini n. sp. resembles D. aestuarina by having a similar number of branchial pairs (8 vs. 7 – 8). However, D. chipolini n. sp. can be distinguished from D. aestuarina by: 1) morphology of the third branchial pair, 2) morphology of the eighth branchial pair if they are present, 3) morphology of neuropodia, and 4) morphology of neuropodial homogomph spinigers. The third pair of branchiae in D. chipolini n. sp. has clavate lobes on both edges of the branchiae, whereas that of D. aestuarina has only one edge with clavate lobes ( Southern 1921: 598, pl. XX, 4F; Fig. 2C View FIGURE 2 , Table 1 View TABLE 1 ). About 50% of the collected specimens of D. chipolini n. sp. have eight pairs of branchiae. When the eighth pair of branchiae is present in D. chipolini n. sp., it is always poorly developed, with a few filaments arising on both edges of the small branchial stem ( Fig. 2E View FIGURE 2 ). In contrast, the eighth branchial pair in D. aestuarina is always fully developed, with many filaments on both edges of the large branchial stem ( Southern 1921: 598, 601). The neuropodia in D. chipolini n. sp. have fewer anterior and posterior lobes in anterior chaetigers than that of D. aestuarina ( Southern 1921: 599 – 601, text-fig. 9; Fig. 3 View FIGURE 3 A–F). Finally, chaetigers 3 to 12 of D. chipolini n. sp. have homogomph spinigers with blunt-tipped short blades with serrations in upper and lower fascicles of neuropodia, whereas D. aestuarina has none of this type of chaetae in neuropodia ( Southern 1921: 600–601, Plate XX, 4L–N; Fig. 4E View FIGURE 4 ).
NMNS # | BL | BW | # pair | 1st | 2nd | 3rd | 4th | 5th | 6th | 7th | 8th |
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LO/ RO | LO/LI/RI/ RO | LO/LI/RI/RO | LO/LI/RI/RO | LO/LI/RI/RO | LO/LI/RI/ RO | LO/LI/RI/RO | LO/LI/RI/ RO | ||||
7861-001 | 105 | 1.3 | 8 | 7/6 | 10/0/5/9 | 8/7/7/9 | 17/15/14/15 | 15/14/14/17 | 16/15/15/18 | 17/14/14/15 | 2/2/1/2 |
7861-002 | 29+ | 1.4 | 8 | 6/5 | 10/0/0/10 | 12/9/8/10 | 16/13/14/14 | 18/17/15/17 | 16/15/16/17 | 11/11/11/12 | 3/2/2/4 |
7861-003 | 93+ | 1.6 | 8 | 5/5 | 9/0/0/9 | 9/8/8/9 | 16/15/15/16 | 16/15/16/17 | 16/15/17/18 | 17/16/17/18 | 7/5 |
7861-004 | 48 | 1.1 | 7 | 6/6 | 9/0/0/11 | 10/9/10/10 | 12/12/13/14 | 12/11/12/13 | 11/10/12/13 | 11/10/11/12 | |
7861-005 | 39+ | 0.6 | 8 | 5/5 | 7/0/0/7 | 8/10/-/- | 11/10/-/- | 12/11/-/- | 14/13/-/- | 10/10/-/- | |
7861-006 | 51+ | 0.8 | 7 | 6/5 | 7/4/-/- | 8/5/6/9 | 13/12/13/14 | 13/12/12/13 | 12/11/13/14 | 11/10/11/12 | |
7861-007 | 75+ | 0.9 | 7 | 5/6 | 10/0/0/8 | 9/6/5/9 | 14/13/12/13 | 13/12/-/- | 15/14/13/14 | 15/14/12/13 | |
7861-008 | 62 | 1.1 | 7 | 6/6 | 9/0/0/9 | 9/7/7/9 | 14/13/14/15 | 16/15/16/15 | 16/15/17/18 | 15/13/14/15 | |
7861-009 | 100+ | 1.4 | 8 | 5/7 | 9/0/0/7 | 11/8/8/13 | 15/14/16/17 | 16/15/17/17 | 19/18/16/17 | 18/17/17/18 | 2/3/8 |
7861-010 | 51+ | 1.4 | 8 | 6/6 | 11/0/0/9 | 11/6/6/10 | 14/13/11/12 | 15/14/14/15 | 16/15/15/16 | 15/14/15/17 | 3/2/5 |
7861-011 | 62+ | 1.1 | 7 | 7/7 | 9/0/0/9 | 9/6/7/9 | 14/12/13/14 | 13/12/14/15 | 13/12/15/16 | 13/12/14/15 | |
7861-012 | 15+ | 1.3 | 8 | 5/5 | 9/0/0/9 | 10/6/6/10 | 15/14/14/15 | 16/15/15/16 | 17/16/15/16 | 15/13/16/14 | 1/3/2 |
7861-013 | 52+ | 1.3 | 7 | 7/6 | 10/0/0/10 | 9/8/5/10 | 15/14/14/15 | 16/16/17/17 | 16/15/16/17 | 14/13/15/16 | |
7861-014 | 44+ | 1.4 | 8 | 6/6 | 8/0/0/8 | 9/6/6/11 | 14/13/13/14 | 15/14/13/15 | 16/15/15/16 | 16/15/16/15 | 1/3/2 |
7861-015 | 27+ | 0.8 | 7 | 6/6 | 8/0/0/8 | 8/7/6/10 | 16/14/12/13 | 14/14/12/13 | 13/12/11/12 | 12/12/11/12 | |
7861-016 | 50+ | 1.1 | 8 | 4/6 | 9/0/0/9 | 8/7/7/10 | 14/13/14/14 | 11/12/14/15 | 14/13/14/15 | -/-/11/12 | |
7861-017 | 36+ | 1.3 | 7 | 6/6 | 8/0/0/8 | 10/7/8/10 | 15/14/16/17 | 16/15/16/17 | 16/17/17/15 | 17/16/16/17 | |
7861-018 | 61+ | 1.3 | 8 | 5/5 | 9/0/0/8 | 8/6/6/8 | 17/16/13/14 | 18/17/15/16 | 16/15/14/15 | 18/17//14/15 | 3/4/3 |
7861-019 | 81+ | 1.6 | 7 | 6/6 | 8/0/0/9 | 8/6/7/9 | 15/14/14/- | 16/14/15/16 | 15/14/14/15 | 13/12/14/15 | |
7861-020 | 27+ | 0.8 | 7 | 7//7 | 8/5/0/7 | 8/6/7/9 | 13/12/10/12 | 14/13/11/13 | 11/10/12/13 | 12/11/10/12 |
NMNS |
National Museum of Natural Science |
VI |
Mykotektet, National Veterinary Institute |
LO |
Type Collection |
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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