Phyllochaetopterus lauensis Rouse, 2007, new species
Phyllochaetopterus lauensis new species (Figs. 1–4) Material Examined .— Holotype (SAMA E 3672), complete, with a tube twice the length of the body and 2 paratypes (SAMA E 3673, OMNH-Iv 5025) complete, with fragments of tube, 5 paratypes (CBM-ZW- 1006, SAM E 3674, SIO-BIC-A 976 and A 977, USNM 11069...
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Biodiversity Taxonomy Animalia Annelida Polychaeta Chaetopteridae Phyllochaetopterus Phyllochaetopterus lauensis |
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Biodiversity Taxonomy Animalia Annelida Polychaeta Chaetopteridae Phyllochaetopterus Phyllochaetopterus lauensis Rouse, Eijiroh Nishi Greg W. Phyllochaetopterus lauensis Rouse, 2007, new species |
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Biodiversity Taxonomy Animalia Annelida Polychaeta Chaetopteridae Phyllochaetopterus Phyllochaetopterus lauensis |
description |
Phyllochaetopterus lauensis new species (Figs. 1–4) Material Examined .— Holotype (SAMA E 3672), complete, with a tube twice the length of the body and 2 paratypes (SAMA E 3673, OMNH-Iv 5025) complete, with fragments of tube, 5 paratypes (CBM-ZW- 1006, SAM E 3674, SIO-BIC-A 976 and A 977, USNM 1106928) incomplete, with a fragment of tube, 1 paratype (USNM 1106929) incomplete, without tube. Holotype and 8 paratypes were collected during dive 145 of the Deep-Sea Research Vehicle (DSV) Jason II at the hydrothermal vent locality known as Hine Hina, Southern Valu Fa Ridge, Lau back-arc basin 22 ° 31.9393S; 176 ° 43.1038W near Tonga on 22 May, 2005, a cluster of chaetopterid tubes was collected by manipulator at 1818 m depth in the vicinity of hydrothermal vents. Additional material examined: For comparison the following Phyllochaetopterus specimens from the Pacific area were also studied: Phyllochaetopterus cf. verrilli Treadwell, 1943: CMNH-ZW-(uncatalogued), Sesoko Island, Okinawa Island, sandy mud flat, 1–2 m deep, February 1987, by E. Nishi. Phyllochaetopterus claparedii McIntosh, 1885: CMNH-ZW-(uncatalogued), Tateyama, Boso Peninsula, 5 to 6m m deep, sandy bottom, by E. Nishi, 15 October 1998. Phyllochaetopterus. sp.: CMNH-ZW (uncatalogued), Port Jackson, Bottle and Glass Rocks, Sydney Harbour, Australia, 33 ° 58 S, 151 0 0 E, 4 m. depth, 4 April 1999 by G. W. Rouse. Diagnosis .— Phyllochaetopterus of small size, eyes absent; A 1 dorsally with short ‘cirri’ with slightly protruding internal chaetae; A 4 with 1–2 stout brown cutting chaetae, pear-shaped in frontal view, head of chaeta slightly inflated, with row of small teeth on both lateral edges. Region B with two chaetigers; B notopodia foliaceous, bilobed; B neuropodia each with single band of uncini; C notopodia digitiform, with single protruding chaeta; C neuropodia bilobed, with two bands of uncini anteriorly, with single band posteriorly. Body formula of species: 9–10 A+ 2 B+ at least ca. 40 C = ca. 52 or more chaetigers; Region A 5 –A 9 of plastron (glandular ventral shield) with distinctive light brown (A 5), whitish (A 6 –A 7), and light brown (A 8 and A 9) transverse bands observed in alcohol-preserved specimens. Tube transparent or translucent, partly amber to white in color, weakly annulated, without septa or partitions. Description (based on holotype). — Holotype complete (some paratypes lacking posterior part of region C), 26 mm long excluding palps; palps, paired 6mm long (about 5 to 8 mm long in paratypes), grooved, arising from near posterolateral border of prostomium (Fig. 3 A). Body 1.0–1.4 mm wide at ventral shield. Body creamy white except for ventral shield in alcohol preserved specimens. Region A narrow, 1.0-1.2mm width, 5.0 mm long for 9 chaetigers (10 chaetigers in some paratypes and 4.0 to 5.0 mm length). Prostomium a distinct lobe, peristomium broad and plate-like, appearing slightly cleft when viewed from ventral side (Fig. 3 A, B, C). Eyespots absent. Cirri of 1 st chaetiger small and short (Fig. 3 A, E), with slightly protruding internal chaetae. Dorsal groove ciliated, extending from base of palps along body regions A, B and C (Fig. 3 E). Ventrum of region A with a long slender plastron (ventral glandular shields), separated into 4 sections based on color (Fig. 3 A, B, C), color of each section varying among type specimens. In holotype, Section I, longer than others, from peristomium to chaetiger A 4 or anterior A 5, white in holotype (Fig. 3 B). In some paratypes (Fig. 3 A and C), pale, very light brown. Section II, chaetiger A 5 only or A 5 to A 6 (Figs. 3 A,C), dark brown in holotype, light or dark brown in paratypes. Section III comprises chaetigers A 6 to A 7 or A 7 only, pale white in holotype and paratypes (Fig. 3 A, B, C). Section IV comprises A 8 and A 9 (plus A 10 in some paratypes) (A 8- 10 in Fig. 3 A; A 7–9 in Fig. 3 B; A 9 in Fig. 3 C), light brown anteriorly and progressively lighter in color in posteriorly in holotype and some paratypes (Fig. 3 A, B), no color in others (Fig. 3 C). In holotype and paratype (SAMA E 3673) Section II darker than anterior Section IV. Chaetigers A 1 to A 3 short, parapodia with a single row of 10 to 20 lanceolate chaetae; A 4 elongate, with one large (cutting) chaeta in each notopodium (one undeveloped chaeta in paratypes CBM-ZW 1006), and more than 10 lanceolate chaetae; A 5 to A 9 (or A 10 in some paratypes) slightly longer and wider than anterior three chaetigers, with single row of 20 to 30 lanceolate chaetae. Cutting chaetae of A 4 with obliquely ellipsoidal distal end; head slightly inflated, slightly wider than shaft, pear-shaped in frontal view, tip slightly pointed (Fig. 4 F, G, H); shaft nearly semi-circular in horizontal section, lateral or ventral grooves absent. Total length of cutting chaetae 300-400 m; head ca. 80 m in width, 90 m in length (Figs. 2 A, B, C, 4 F, G, H). Middle region (region B) comprises 2 chaetigers only, each slightly longer than anterior chaetigers; notopodia bilobed, dorsal lobe branched into a Y-shape (= dichotomously branched) (Fig. 3 A, B, C, D). Paddle and cupule absent. B 1 and B 2 nearly same length. Beneath last A chaetiger and first B notopodia, a pair of liquidfilled swellings present (Fig. 3 D). B-region neuropodia unilobed with one row of minute uncini: uncini nearly triangular, with ca. 25 teeth (Fig. 4 J). Posterior region (region C) with 25 chaetigers in holotype (up to 40 chaetigers in three paratypes, though incomplete). Anterior C-region chaetigers elongate, extended and longer than regions A and B chaetigers (Figs. 3 A, 4 A). Notopodia unilobed, knob-like tip each with a single chaeta (Fig. 4 A, B, C). Neuropodia bilobed in anterior 10 to 12 chaetigers (Fig. 4 A, B) and unilobed in posterior chaetigers (Fig. 4 C). Uncini similar to those of region-B, but smaller. Tube fragile, 1.5 to 2.0 mm in diameter, slender, nearly straight, weakly annulated and pleated in parts. Tube wall thin, transparent, partly light amber to light brown. Septa or partitions absent. Etymology .—The species epithet lauensis is derived from the name of the type locality, the Lau back-arc basin. Remarks. —Among the Phyllochaetopterus , P. lauensis n. sp. is easily distinguishable from other members of the genus by its alternating white/brown patterning on the plastron. Similar patterning is found in Spiochaetopterus spp. (e.g., Bhaud, 1998; Nishi et al., 2004), and the feature is used for distinguishing among the species of this genus. In Phyllochaetopterus , however, the ventral shield (glandular area) is usually a single color or separated into only two colored portions, anterior and posterior. For Phyllochaetopterus in general, the A 4 chaetal numbers and color, the number of region-B chaetigers and tube characters are used for distinguishing species. Based on those characters, we provide here a summary table (Table 1). *H.-S. = Hartmann-Schröder Among the 19 previously described species of Phyllochaetopterus , twelve species have 1–2 cutting chaetae on notopodia of A 4, while others have a row of 3–8 cutting chaetae (Table 1, Bhaud 1977, Kudenov 1975). These taxa can also be distinguished further by the number of region-B chaetigers and separated into four groups (Table 1): A—having 1–2 cutting chaetae in A 4 notopodia, with two region-B chaetigers; B—having 1–2 cutting chaetae in A 4, with three or more region-B chaetigers; C—having a row of more than 6 cutting chaetae in A 4, with two region-B chaetigers; D—having more than 6 cutting chaetae in A 4, with three or more region-B chaetigers. Phyllochaetopterus lauensis n. sp. belongs in group A, which now contains 4 described species; P. gracilis Grube, 1863, P. claparedii McIntosh, 1885, P. limicolus Hartman, 1960 and P. monroi Hartman, 1967. Apart from all other Phyllochaetopterus lacking the marked patterning described here for P. lauensis n. sp., Phyllochaetopterus gracilis has 10–11 region-A chaetigers whereas P. lauensis n. sp. has only 9–10. Phyllochaetopterus limicolus lacks the inflated head in A 4 modified chaetae (Bhaud 1977) seen in P. lauensis n. sp. (Fig. 2 B, C). Phyllochaetopterus claparedii is morphologically most similar to P. lauensis n. sp., but the former has long, clavate cirri on A 1 and region-B chaetigers are elongate and longer than those of region A (McIntosh 1885). Phyllochaetopterus lauensis n. sp. on the other hand has short cirri on A 1, and region-B chaetigers are not especially elongate (Fig. 3 A, E). Additionally, P. lauensis n. sp. is also distinguishable from P . claparedii by the number of chaetae in the C notopodia; P. claparedii and P. aciculigerus have 3–4 chaetae in posterior C notopodia and all other species of the genus have only a single chaeta. P. monroi Hartman has minute papillae at the base of C notopodia, whereas P. lauensis n. sp has no such papillae. We also compared the new species to specimens of P. claparedii collected at Tateyama, Boso Peninsula, Chiba Prefecture, particularly with regards to the A 4 chaetal structure using scanning electron microscopy. Phyllochaetopterus lauensis n. sp. and P. claparedii both have 9–10 A+ 2 B, and 1–2 A 4 cutting chaetae with a slightly inflated head with a slanting edge in lateral view (Fig. 2 A, F). However, in frontal view the A 4 cutting chaetae of P. lauensis are pear-shaped (Fig. 2 A–C) and those of P. claparedii are asymmetrically cordate - a skewed heart shape (Fig. 2 E, F). : Published as part of Rouse, Eijiroh Nishi Greg W., 2007, A new species of Phyllochaetopterus (Chaetopteridae: Annelida) from near hydrothermal vents in the Lau Basin, western Pacific Ocean, pp. 55-64 in Zootaxa 1621 on pages 56-62, DOI: 10.5281/zenodo.179205 : {"references": ["Treadwell, A. (1943) New species of polychaetous annelids from Hawaii. Annales Magazine Novitates, 1233, 1 - 4. Willey, A. (1905) Report on the Polychaeta collected by Professor Herdman, at Ceylon, in 1902. Ceylon Pearl Oyster Fisheries, Supplementary Report, 30 (4), 243 - 324.", "McIntosh, W. C. (1885) Report on the Annelida Polychaeta collected by H. M. S. Challenger during the years 1873 - 76. Reports of the Scientific Results of the Voyage of H. M. S. Challenger during the Years 1873 - 76, Zoology, 12, 1 - 554.", "Bhaud, M. (1998) The species of the genus Spiochaetopterus (Polychaeta, Chaetopteridae) in the Atlantic-Mediterranean biogeographic area. Sarsia, 83, 243 - 263.", "Nishi, E., Bhaud, M. & Koh, B. - S. (2004) Two new species of Spiochaetopterus (Annelida: Polychaeta) from Sagami Bay and Tokyo Bay, central Japan with a comparative table of species from Japanese and adjacent waters. Zoological Science, 21, 457 - 464.", "Bhaud, M. (1977) Note sur quelques representants du genre Phyllochaetopterus (Annelides Polychetes) et observations au microscope a balayage des soies specialisees. Vie et Milieu, 27 (1 A), 11 - 33.", "Kudenov, J. (1975) Sedentary polychaetes from the Gulf of California, Mexico. Journal of Natural History, 9, 205 - 231.", "Grube, E. (1863) Beschreibung neuer oder wenig bekannter Anneliden; 5: Beitrag: Zahlreiche Gattungen. Archivos Naturgeschrichten, 29, 37 - 69.", "Hartman, O. (1960) Systematic account of some marine invertebrate animals from the deep basins off southern California. Part II. Allan Hancock Pacific Expeditions, 22, 69 - 215.", "Hartman, O. (1967) Polychaetous annelids collected by the USNS Eltanin and Staten Island cruises, chiefly from Antarctic seas. 386 pp."]} |
format |
Text |
author |
Rouse, Eijiroh Nishi Greg W. |
author_facet |
Rouse, Eijiroh Nishi Greg W. |
author_sort |
Rouse, Eijiroh Nishi Greg W. |
title |
Phyllochaetopterus lauensis Rouse, 2007, new species |
title_short |
Phyllochaetopterus lauensis Rouse, 2007, new species |
title_full |
Phyllochaetopterus lauensis Rouse, 2007, new species |
title_fullStr |
Phyllochaetopterus lauensis Rouse, 2007, new species |
title_full_unstemmed |
Phyllochaetopterus lauensis Rouse, 2007, new species |
title_sort |
phyllochaetopterus lauensis rouse, 2007, new species |
publisher |
Zenodo |
publishDate |
2007 |
url |
https://dx.doi.org/10.5281/zenodo.5667261 https://zenodo.org/record/5667261 |
long_lat |
ENVELOPE(7.990,7.990,63.065,63.065) ENVELOPE(168.683,168.683,-77.517,-77.517) ENVELOPE(67.150,67.150,-67.750,-67.750) ENVELOPE(-144.850,-144.850,-77.017,-77.017) ENVELOPE(-60.526,-60.526,-72.655,-72.655) ENVELOPE(69.642,69.642,-48.773,-48.773) |
geographic |
Antarctic Pacific Tonga McIntosh Rouse Treadwell Herdman Glass Rocks |
geographic_facet |
Antarctic Pacific Tonga McIntosh Rouse Treadwell Herdman Glass Rocks |
genre |
Antarc* Antarctic |
genre_facet |
Antarc* Antarctic |
op_relation |
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op_rights |
Open Access info:eu-repo/semantics/openAccess |
op_doi |
https://doi.org/10.5281/zenodo.5667261 https://doi.org/10.5281/zenodo.179205 https://doi.org/10.5281/zenodo.179206 https://doi.org/10.5281/zenodo.179207 https://doi.org/10.5281/zenodo.179208 https://doi.org/10.5281/zenodo.179209 https://doi.or |
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ftdatacite:10.5281/zenodo.5667261 2023-05-15T13:50:00+02:00 Phyllochaetopterus lauensis Rouse, 2007, new species Rouse, Eijiroh Nishi Greg W. 2007 https://dx.doi.org/10.5281/zenodo.5667261 https://zenodo.org/record/5667261 unknown Zenodo http://publication.plazi.org/id/771EFFA7FF82FF834A27FFD99924DF17 http://table.plazi.org/id/57F16641FF84FF854AB0FDFE9884DD93 http://zoobank.org/CCA11363-80D4-4C87-8557-52B9B7D89047 https://zenodo.org/communities/biosyslit https://dx.doi.org/10.5281/zenodo.179205 http://publication.plazi.org/id/771EFFA7FF82FF834A27FFD99924DF17 https://dx.doi.org/10.5281/zenodo.179206 https://dx.doi.org/10.5281/zenodo.179207 https://dx.doi.org/10.5281/zenodo.179208 https://dx.doi.org/10.5281/zenodo.179209 http://table.plazi.org/id/57F16641FF84FF854AB0FDFE9884DD93 http://zoobank.org/CCA11363-80D4-4C87-8557-52B9B7D89047 https://dx.doi.org/10.5281/zenodo.5667262 https://zenodo.org/communities/biosyslit Open Access info:eu-repo/semantics/openAccess Biodiversity Taxonomy Animalia Annelida Polychaeta Chaetopteridae Phyllochaetopterus Phyllochaetopterus lauensis Taxonomic treatment article-journal Text ScholarlyArticle 2007 ftdatacite https://doi.org/10.5281/zenodo.5667261 https://doi.org/10.5281/zenodo.179205 https://doi.org/10.5281/zenodo.179206 https://doi.org/10.5281/zenodo.179207 https://doi.org/10.5281/zenodo.179208 https://doi.org/10.5281/zenodo.179209 https://doi.or 2022-02-08T13:29:49Z Phyllochaetopterus lauensis new species (Figs. 1–4) Material Examined .— Holotype (SAMA E 3672), complete, with a tube twice the length of the body and 2 paratypes (SAMA E 3673, OMNH-Iv 5025) complete, with fragments of tube, 5 paratypes (CBM-ZW- 1006, SAM E 3674, SIO-BIC-A 976 and A 977, USNM 1106928) incomplete, with a fragment of tube, 1 paratype (USNM 1106929) incomplete, without tube. Holotype and 8 paratypes were collected during dive 145 of the Deep-Sea Research Vehicle (DSV) Jason II at the hydrothermal vent locality known as Hine Hina, Southern Valu Fa Ridge, Lau back-arc basin 22 ° 31.9393S; 176 ° 43.1038W near Tonga on 22 May, 2005, a cluster of chaetopterid tubes was collected by manipulator at 1818 m depth in the vicinity of hydrothermal vents. Additional material examined: For comparison the following Phyllochaetopterus specimens from the Pacific area were also studied: Phyllochaetopterus cf. verrilli Treadwell, 1943: CMNH-ZW-(uncatalogued), Sesoko Island, Okinawa Island, sandy mud flat, 1–2 m deep, February 1987, by E. Nishi. Phyllochaetopterus claparedii McIntosh, 1885: CMNH-ZW-(uncatalogued), Tateyama, Boso Peninsula, 5 to 6m m deep, sandy bottom, by E. Nishi, 15 October 1998. Phyllochaetopterus. sp.: CMNH-ZW (uncatalogued), Port Jackson, Bottle and Glass Rocks, Sydney Harbour, Australia, 33 ° 58 S, 151 0 0 E, 4 m. depth, 4 April 1999 by G. W. Rouse. Diagnosis .— Phyllochaetopterus of small size, eyes absent; A 1 dorsally with short ‘cirri’ with slightly protruding internal chaetae; A 4 with 1–2 stout brown cutting chaetae, pear-shaped in frontal view, head of chaeta slightly inflated, with row of small teeth on both lateral edges. Region B with two chaetigers; B notopodia foliaceous, bilobed; B neuropodia each with single band of uncini; C notopodia digitiform, with single protruding chaeta; C neuropodia bilobed, with two bands of uncini anteriorly, with single band posteriorly. Body formula of species: 9–10 A+ 2 B+ at least ca. 40 C = ca. 52 or more chaetigers; Region A 5 –A 9 of plastron (glandular ventral shield) with distinctive light brown (A 5), whitish (A 6 –A 7), and light brown (A 8 and A 9) transverse bands observed in alcohol-preserved specimens. Tube transparent or translucent, partly amber to white in color, weakly annulated, without septa or partitions. Description (based on holotype). — Holotype complete (some paratypes lacking posterior part of region C), 26 mm long excluding palps; palps, paired 6mm long (about 5 to 8 mm long in paratypes), grooved, arising from near posterolateral border of prostomium (Fig. 3 A). Body 1.0–1.4 mm wide at ventral shield. Body creamy white except for ventral shield in alcohol preserved specimens. Region A narrow, 1.0-1.2mm width, 5.0 mm long for 9 chaetigers (10 chaetigers in some paratypes and 4.0 to 5.0 mm length). Prostomium a distinct lobe, peristomium broad and plate-like, appearing slightly cleft when viewed from ventral side (Fig. 3 A, B, C). Eyespots absent. Cirri of 1 st chaetiger small and short (Fig. 3 A, E), with slightly protruding internal chaetae. Dorsal groove ciliated, extending from base of palps along body regions A, B and C (Fig. 3 E). Ventrum of region A with a long slender plastron (ventral glandular shields), separated into 4 sections based on color (Fig. 3 A, B, C), color of each section varying among type specimens. In holotype, Section I, longer than others, from peristomium to chaetiger A 4 or anterior A 5, white in holotype (Fig. 3 B). In some paratypes (Fig. 3 A and C), pale, very light brown. Section II, chaetiger A 5 only or A 5 to A 6 (Figs. 3 A,C), dark brown in holotype, light or dark brown in paratypes. Section III comprises chaetigers A 6 to A 7 or A 7 only, pale white in holotype and paratypes (Fig. 3 A, B, C). Section IV comprises A 8 and A 9 (plus A 10 in some paratypes) (A 8- 10 in Fig. 3 A; A 7–9 in Fig. 3 B; A 9 in Fig. 3 C), light brown anteriorly and progressively lighter in color in posteriorly in holotype and some paratypes (Fig. 3 A, B), no color in others (Fig. 3 C). In holotype and paratype (SAMA E 3673) Section II darker than anterior Section IV. Chaetigers A 1 to A 3 short, parapodia with a single row of 10 to 20 lanceolate chaetae; A 4 elongate, with one large (cutting) chaeta in each notopodium (one undeveloped chaeta in paratypes CBM-ZW 1006), and more than 10 lanceolate chaetae; A 5 to A 9 (or A 10 in some paratypes) slightly longer and wider than anterior three chaetigers, with single row of 20 to 30 lanceolate chaetae. Cutting chaetae of A 4 with obliquely ellipsoidal distal end; head slightly inflated, slightly wider than shaft, pear-shaped in frontal view, tip slightly pointed (Fig. 4 F, G, H); shaft nearly semi-circular in horizontal section, lateral or ventral grooves absent. Total length of cutting chaetae 300-400 m; head ca. 80 m in width, 90 m in length (Figs. 2 A, B, C, 4 F, G, H). Middle region (region B) comprises 2 chaetigers only, each slightly longer than anterior chaetigers; notopodia bilobed, dorsal lobe branched into a Y-shape (= dichotomously branched) (Fig. 3 A, B, C, D). Paddle and cupule absent. B 1 and B 2 nearly same length. Beneath last A chaetiger and first B notopodia, a pair of liquidfilled swellings present (Fig. 3 D). B-region neuropodia unilobed with one row of minute uncini: uncini nearly triangular, with ca. 25 teeth (Fig. 4 J). Posterior region (region C) with 25 chaetigers in holotype (up to 40 chaetigers in three paratypes, though incomplete). Anterior C-region chaetigers elongate, extended and longer than regions A and B chaetigers (Figs. 3 A, 4 A). Notopodia unilobed, knob-like tip each with a single chaeta (Fig. 4 A, B, C). Neuropodia bilobed in anterior 10 to 12 chaetigers (Fig. 4 A, B) and unilobed in posterior chaetigers (Fig. 4 C). Uncini similar to those of region-B, but smaller. Tube fragile, 1.5 to 2.0 mm in diameter, slender, nearly straight, weakly annulated and pleated in parts. Tube wall thin, transparent, partly light amber to light brown. Septa or partitions absent. Etymology .—The species epithet lauensis is derived from the name of the type locality, the Lau back-arc basin. Remarks. —Among the Phyllochaetopterus , P. lauensis n. sp. is easily distinguishable from other members of the genus by its alternating white/brown patterning on the plastron. Similar patterning is found in Spiochaetopterus spp. (e.g., Bhaud, 1998; Nishi et al., 2004), and the feature is used for distinguishing among the species of this genus. In Phyllochaetopterus , however, the ventral shield (glandular area) is usually a single color or separated into only two colored portions, anterior and posterior. For Phyllochaetopterus in general, the A 4 chaetal numbers and color, the number of region-B chaetigers and tube characters are used for distinguishing species. Based on those characters, we provide here a summary table (Table 1). *H.-S. = Hartmann-Schröder Among the 19 previously described species of Phyllochaetopterus , twelve species have 1–2 cutting chaetae on notopodia of A 4, while others have a row of 3–8 cutting chaetae (Table 1, Bhaud 1977, Kudenov 1975). These taxa can also be distinguished further by the number of region-B chaetigers and separated into four groups (Table 1): A—having 1–2 cutting chaetae in A 4 notopodia, with two region-B chaetigers; B—having 1–2 cutting chaetae in A 4, with three or more region-B chaetigers; C—having a row of more than 6 cutting chaetae in A 4, with two region-B chaetigers; D—having more than 6 cutting chaetae in A 4, with three or more region-B chaetigers. Phyllochaetopterus lauensis n. sp. belongs in group A, which now contains 4 described species; P. gracilis Grube, 1863, P. claparedii McIntosh, 1885, P. limicolus Hartman, 1960 and P. monroi Hartman, 1967. Apart from all other Phyllochaetopterus lacking the marked patterning described here for P. lauensis n. sp., Phyllochaetopterus gracilis has 10–11 region-A chaetigers whereas P. lauensis n. sp. has only 9–10. Phyllochaetopterus limicolus lacks the inflated head in A 4 modified chaetae (Bhaud 1977) seen in P. lauensis n. sp. (Fig. 2 B, C). Phyllochaetopterus claparedii is morphologically most similar to P. lauensis n. sp., but the former has long, clavate cirri on A 1 and region-B chaetigers are elongate and longer than those of region A (McIntosh 1885). Phyllochaetopterus lauensis n. sp. on the other hand has short cirri on A 1, and region-B chaetigers are not especially elongate (Fig. 3 A, E). Additionally, P. lauensis n. sp. is also distinguishable from P . claparedii by the number of chaetae in the C notopodia; P. claparedii and P. aciculigerus have 3–4 chaetae in posterior C notopodia and all other species of the genus have only a single chaeta. P. monroi Hartman has minute papillae at the base of C notopodia, whereas P. lauensis n. sp has no such papillae. We also compared the new species to specimens of P. claparedii collected at Tateyama, Boso Peninsula, Chiba Prefecture, particularly with regards to the A 4 chaetal structure using scanning electron microscopy. Phyllochaetopterus lauensis n. sp. and P. claparedii both have 9–10 A+ 2 B, and 1–2 A 4 cutting chaetae with a slightly inflated head with a slanting edge in lateral view (Fig. 2 A, F). However, in frontal view the A 4 cutting chaetae of P. lauensis are pear-shaped (Fig. 2 A–C) and those of P. claparedii are asymmetrically cordate - a skewed heart shape (Fig. 2 E, F). : Published as part of Rouse, Eijiroh Nishi Greg W., 2007, A new species of Phyllochaetopterus (Chaetopteridae: Annelida) from near hydrothermal vents in the Lau Basin, western Pacific Ocean, pp. 55-64 in Zootaxa 1621 on pages 56-62, DOI: 10.5281/zenodo.179205 : {"references": ["Treadwell, A. (1943) New species of polychaetous annelids from Hawaii. Annales Magazine Novitates, 1233, 1 - 4. Willey, A. (1905) Report on the Polychaeta collected by Professor Herdman, at Ceylon, in 1902. Ceylon Pearl Oyster Fisheries, Supplementary Report, 30 (4), 243 - 324.", "McIntosh, W. C. (1885) Report on the Annelida Polychaeta collected by H. M. S. Challenger during the years 1873 - 76. Reports of the Scientific Results of the Voyage of H. M. S. Challenger during the Years 1873 - 76, Zoology, 12, 1 - 554.", "Bhaud, M. (1998) The species of the genus Spiochaetopterus (Polychaeta, Chaetopteridae) in the Atlantic-Mediterranean biogeographic area. Sarsia, 83, 243 - 263.", "Nishi, E., Bhaud, M. & Koh, B. - S. (2004) Two new species of Spiochaetopterus (Annelida: Polychaeta) from Sagami Bay and Tokyo Bay, central Japan with a comparative table of species from Japanese and adjacent waters. Zoological Science, 21, 457 - 464.", "Bhaud, M. (1977) Note sur quelques representants du genre Phyllochaetopterus (Annelides Polychetes) et observations au microscope a balayage des soies specialisees. Vie et Milieu, 27 (1 A), 11 - 33.", "Kudenov, J. (1975) Sedentary polychaetes from the Gulf of California, Mexico. Journal of Natural History, 9, 205 - 231.", "Grube, E. (1863) Beschreibung neuer oder wenig bekannter Anneliden; 5: Beitrag: Zahlreiche Gattungen. Archivos Naturgeschrichten, 29, 37 - 69.", "Hartman, O. (1960) Systematic account of some marine invertebrate animals from the deep basins off southern California. Part II. Allan Hancock Pacific Expeditions, 22, 69 - 215.", "Hartman, O. (1967) Polychaetous annelids collected by the USNS Eltanin and Staten Island cruises, chiefly from Antarctic seas. 386 pp."]} Text Antarc* Antarctic DataCite Metadata Store (German National Library of Science and Technology) Antarctic Pacific Tonga ENVELOPE(7.990,7.990,63.065,63.065) McIntosh ENVELOPE(168.683,168.683,-77.517,-77.517) Rouse ENVELOPE(67.150,67.150,-67.750,-67.750) Treadwell ENVELOPE(-144.850,-144.850,-77.017,-77.017) Herdman ENVELOPE(-60.526,-60.526,-72.655,-72.655) Glass Rocks ENVELOPE(69.642,69.642,-48.773,-48.773) |