Perinereis mictodonta ( Marenzeller, 1879 )

Hsueh, Pan-Wen, 2024, Positive association between PTN polymorphisms and schizophrenia in Northeast Chinese Han population., Zoological Studies 63 (39), pp. 141-149 : 30-32

publication ID

https://doi.org/10.6620/ZS.2024.63-39

persistent identifier

https://treatment.plazi.org/id/BA245356-1076-FFCC-FCF9-68D41213FC82

treatment provided by

Felipe

scientific name

Perinereis mictodonta ( Marenzeller, 1879 )
status

 

Perinereis mictodonta ( Marenzeller, 1879) View in CoL ( Fig. 15 View Fig , Table 3)

Nereis mictodonta Marenzeller 1879: 118–119 View in CoL , pl. 2, fig. 2; Izuka, 1912: 148–151, pl. 16, figs. 1–6.

Perinereis mictodonta Wilson and Glasby 1993: 264 View in CoL ; Glasby and Hsieh 2006: 558–561, fig. 5 (for complete synonym).

Material examined: 2 specimens, NMNS 1955- 22, Kaomei (24°18.50'N, 120°32.42'E), habitat type: ISSB, 10 November 1992; 3 specimens, NMNS 8748- 67, Da’an (24°22.29'N, 120°34.70'E), habitat type: ISSB, 30 January, 1999; 1 specimen, NMNS 8748- 68, Kaomei (24°18.50'N, 120°32.42'E), habitat type: ISSB, 24 August, 1999; 2 specimens, NMNS 3328- 112, Hanbao (24°00.75'N, 120°21.11'E), habitat type: ISSB, 1 February 2000; 1 specimen, NMNS 8748- 69, Wushibi (23°13.70'N, 121°25.08'E), habitat type: IRHB, 16 October 2004; 1 specimen, NMNS 8748- 70, Bazang (23°19.51'N, 120°07.78'E), habitat type: ISSB, 7 January, 2007; 7 specimens, NMNS 8748- 71–78, Fubao (24°02.83'N, 120°22.75'E), habitat type: ISSB, 29 January, 2007; 1 specimen, NMNS 8748-79, Wanggong (23°58.36'N, 120°19.43'E), habitat type: ISSB, 29 January, 2007; 13 specimens, NMNS 8748- 80–83, Fubao, 2 March 2007; 4 specimens, NMNS 8748-84–87, Fuxin (24°03.40'N, 120°24.50'E), habitat type: ISSB, 18 March, 2007; 4 specimens, NMNS 8748- 88–91, Dadu (24°12.77'N, 120°28.06'E), habitat type: ISSB, 20 March 2015; 4 specimens, NMNS 8748-92, Hemei (25°04.91'N, 121°54.93'E), habitat type: ISSB, 17 October 2016.

Description: Based on eight complete specimens ( NMNS 8748-69, NMNS 8748-71–73, NMNS 8748- 79, NMNS 8748-83(1), NMNS 8748-90–91; all atoke) and 14 incomplete specimens ( NMNS 1559-22, NMNS 8748-67(1) –68, NMNS 3328-112, NMNS 8748-70, NMNS 8748-75–78, NMNS 8748-81–82, NMNS 8748- 84–85; all atoke): Body length 41.0–103.0 (n = 8) mm with 82–151 (n = 8) chaetigers, chaetiger 10 width 1.1– 4.0 (n = 22) mm, excluding parapodia; beige in alcohol ( Fig. 15A, B View Fig ). Prostomium wider than long, lateral antennae antero-lateral, shorter than palps, palpophores globose, palpostyles spheroid. Four pairs of tentacular cirri, longest one reaching chaetiger 3–13 (n = 20). Two pairs of eyes, in trapezoidal arrangement. Tentacular belt about 1.1–1.4x (n = 21) longer than chaetiger 1. Pharynx with dark brown jaws, each with 3–6 (n = 22) teeth; paragnath pattern: I = 1–6 (mostly 2–5, in cluster or longitudinal line, one case of 1 and two cases of 6, n = 22, same sample size on following areas); II = 14–26 (left), 12–25 (right), in 2–4 oblique rows; III = 15–32 (center region with 11–24 cones, in 3–4 transverse rows; mostly 2 lateral regions, each with 1–6 cones, three case of 3 lateral regions, outer region with 1–2 cones); IV = 23–42 (left), 23–42 (right), in 3–7 oblique rows, without bars; V = 1–4 (mostly 3, in triangle or transverse row, one case of 1 cone, two cases of 2 cones, four cases of 4 cones); VI = 3–9 uneven-length bars, innermost and outermost longest (left), 3–8 uneven-length bars, innermost and outermost longest (right); VII –VIII = 20– 39, in 2 rows, posterior row zigzagged. Ridge pattern of areas VI – V – VI, χ-shaped ( Fig. 15A, B View Fig , Table 3).

Dorsal cirri digitiform, medially attached dorsal ligule throughout, about 0.8x as long as dorsal ligule on anterior to mid-body chaetigers, about 0.5x as long as dorsal ligule on posterior chaetigers ( Fig. 15C–E View Fig , Table 3).

Dorsal ligule subconical throughout, about 2.0x longer than median ligule on anterior to mid-body chaetigers, about 1.3x longer than median ligule on posterior chaetigers; center lobe of dorsal ligule with one irregular-shaped glandular mass on posterior chaetigers ( Fig. 15C–E View Fig ). Notopodial prechaetal lobe absent ( Table 3).

Median ligule subconical throughout, greatly longer than neuroacicular ligule throughout ( Fig. 15C– E View Fig ).

Neuroacicular ligule with prominent inferior lobe on anterior to mid-body chaetigers, about as long as ventral ligule, inferior and superior lobes subequal in length on posterior chaetigers, about as long as ventral ligule. Neuropodial postchaetal lobe absent. Ventral cirri digitiform, mid-ventrally attached to ventral edge of parapodia on anterior to mid-body chaetigers, about 0.9x as long as ventral ligule, distally attached to ventral ligule on posterior chaetigers, about 0.6x as long as ventral ligule ( Fig. 15C–E View Fig ).

Notochaetae present from chaetiger 3 to posterior chaetigers, homogomph spinigers present throughout. Supra-acicular fascicle of neuropodia: homogomph spinigers and medium-sized blade heterogomph falcigers with serrations present throughout. Subacicular fascicle of neuropodia: medium-sized blade heterogomph falcigers with serrations and heterogomph spinigers present throughout ( Fig. 15F View Fig , Table 3).

Pygidium with anus crenulated; anal cirri cirriform, as long as last 4–8 (n = 5) chaetigers.

Remarks: The morphology of examined specimens in the present study agrees with description of P. mictodonta ( Marenzeller, 1879) in Glasby and Hsieh (2006: 599–561, fig. 5A–F) ( Fig. 15A–F View Fig , Table 3). All examined specimens of P. mictodonta in the present study were mostly collected from soft bottom on river mouths and coastal flats of central-west Taiwan, which largely agree with distribution of this species in Taiwan reported by Glasby and Hsieh (2006: 555, fig. 1). Glasby and Hsieh (2006: 555, fig. 1) commented that no polychaete in the Perinereis nuntia group were found from river mouths on east coasts of Taiwan. However, the present distribution record of P. mictodonta in Taiwan showed one exception. One specimen of P. mictodonta was collected from rocky tide pool in coasts of Wushibi, eastern Taiwan. Presumably, windy seasons on east coasts of Taiwan provide suitable temporal living environment in rocky tide pool (i.e., sediment and algae brought in by strong wave actions) for larvae of P. mictodonta to settle and grow in that environment. This favorable living environment of biota vanished during summer with weak wave actions and high evaporation.

NMNS

National Museum of Natural Science

V

Royal British Columbia Museum - Herbarium

VI

Mykotektet, National Veterinary Institute

Kingdom

Animalia

Phylum

Annelida

Class

Polychaeta

Order

Phyllodocida

Family

Nereididae

Genus

Perinereis

Loc

Perinereis mictodonta ( Marenzeller, 1879 )

Hsueh, Pan-Wen 2024
2024
Loc

Perinereis mictodonta

Glasby CJ & Hsieh H-L. 2006: 558
Wilson RS & Glasby CJ 1993: 264
1993
Loc

Nereis mictodonta

Izuka A. 1912: 148
Marenzeller E von 1879: 119
1879
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