Leocrates reishi, Salazar-Vallejo, 2020

Salazar-Vallejo, Sergio I., 2020, Revision of Leocrates Kinberg, 1866 and Leocratides Ehlers, 1908 (Annelida, Errantia, Hesionidae), Zootaxa 4739 (1), pp. 1-114 : 66-68

publication ID

https://doi.org/ 10.11646/zootaxa.4739.1.1

publication LSID

lsid:zoobank.org:pub:544B9C82-BF33-4EA1-9411-E1A307137466

DOI

https://doi.org/10.5281/zenodo.3680197

persistent identifier

https://treatment.plazi.org/id/2D1987E4-FFA2-736F-FF23-FF6FF5FF6254

treatment provided by

Plazi

scientific name

Leocrates reishi
status

sp. nov.

Leocrates reishi View in CoL n. sp.

Figs 36 View FIGURE 36 , 37 View FIGURE 37

urn:lsid:zoobank.org:act:B9292D1D-04DA-41A6-B4BA-D28B5FE34270

Leocrates chinensis: Hartman 1954: 622 View in CoL (Bikini and Eniwetok atolls), 625 (outside Bikini atoll, Lidilbut Island, Eniwetok atoll), 628 (systematic list); Reish 1968: 213; Pettibone 1970: 215 (listed specimen; not described nor illustrated); Bailey-Brock & Hartman 1987: 262–263, Fig. 3 View FIGURE 3 .II.33 (all partim, non Kinberg, 1866).

Type material. Western Pacific. Marshall Islands. Holotype ( LACM 10883 View Materials ), Ralik Chain , Eniwetok Atoll, Lidilbut Island, corals, Sta. 1504 (no further data), May 1952, H.S. Ladd, coll. Paratype ( LACM 10884 View Materials ), Ralik Chain , Eniwetok Atoll, Lidilbut Island, corals, Sta. 1503 (no further data), May 1952, H.S. Ladd, coll. [complete. Brownish, posterior region bent dorsally, most notochaetae and cirri missing; a lateral ventral dissection made to observe pharynx jaws; right parapodium of chaetiger 12 dissected (kept in container). Body 19 mm long, 2 mm wide, 16 chaetigers. Anterior eyes emarginate, twice larger than posterior round ones. Notochaetae with coarse subdistal denticulation; notacicular lobe blunt, neuracicular lobe round, about as long as wide; neurochaetae with blades bidentate, guard approaching subdistal tooth. Oocytes not seen; testis with spermatids in parapodia] .

Additional material. Western Pacific. Philippines. One specimen ( LACM 10142 View Materials ), Palawan, Honda Bay (09°54’02.5200” N, 118°43’21.3600” E), seagrass bed, under coral rubble, 1.2 m, 18 Apr. 1995, K. Fitzhugh, coll. [middle 17 mm long, 2 mm wide] GoogleMaps . New Caledonia. One specimen ( UF 4016 ), Poum Pass (20°16’22.44” S, 163°52’48.72” W), back reef, patch coral, 0–2 m, 12 Nov. 2013, N. Evans, coll. [18 mm long, 2 mm wide] GoogleMaps .

French Polynesia. One specimen ( UF 1433 ), Society Islands , Moorea, Atiha Bay, west side of pass (17°35’44.52” S, 149°50’44.16” W), barrier reef, 0.5–1.0 m, 8 Dec. 2009, S. McPherson & G. Paulay, coll. [16 mm long, 2 mm wide] GoogleMaps .

Description. Holotype (LACM 10883) complete, slightly bent ventrally. Body with parallel sides ( Fig. 36A View FIGURE 36 ), blunt anteriorly, slightly tapered posteriorly, 20 mm long, 3 mm wide, 16 chaetigers; right parapodium of chaetiger 7 dissected (kept in container). Most tentacular, dorsal and ventral cirri on site. Body brownish, cirri paler, eyes brown.

Prostomium wider than long, slightly wider anteriorly ( Fig. 36B View FIGURE 36 ). Lateral antennae with ceratophores distinct, antennae slightly longer than prostomium (1.2 times as long), 1.2–1.5 times longer than palps; palpophores 2–3 times longer than palpostyles (palpostyles darker along basal half). Median antenna short, surpassing prostomial centre, not reaching prostomial anterior margin, inserted between posterior eyes.

Eyes dark brown, right eyes darker; anterior eyes each 1 / 15 prostomial width, twice larger than posterior ones, slightly emarginate anterolaterally, and more distant to each other than posterior, round eyes.

Nuchal organs lobes horizontal C-shaped, completely concealed by anterior margin of tentacular belt; lateral ciliated bands narrow, not visible dorsally. Tentacular cirri almost complete, twisted, without tips, longer ones reaching chaetiger 7. Lateral cushions low, entire, slightly projected along middle chaetigers. Longitudinal striae visible along body.

Pharynx fully exposed ( Fig. 36C View FIGURE 36 ), slightly expanded distally. Lateral vesicles present only on right side, globular, not tapered. Anterior margin with about 30 irregularly defined lobes. Dorsal and ventral jaws single, brownish, exposed, tapered, ventral jaw smaller than dorsal one.

Dorsal cirri as long as body width (including parapodia). Chaetigers 1–4 without notochaetae; notochaetae present along chaetigers 5–16, sparse (about 30 per bundle), delicate (some parapodia with notochaetae broken), some arranged as transverse fans, notochaetae subdistally denticulate, denticles coarse (visible in 10x). Notacicular lobes blunt, neuracicular lobes projected, blunt, as long as wide ( Fig. 36D View FIGURE 36 ). Neurochaetae about 20 per bundle, blades decreasing in size ventrally, bidentate, 3–12 times longer than wide, guards approaching subdistal tooth ( Fig. 36D View FIGURE 36 , insets).

Posterior region tapered. Prepygidial segment with dorsal cirri 3–4 times longer than ventral ones. Pygidium not projected, anus dorsoterminal, anal cirri missing.

Oocytes not seen.

Etymology. This species is named after the late Dr. Donald J. Reish in recognition of his many publications on several critical localities (including San Quintín and Los Angeles bays in Western Mexico), and especially after his study on the polychaetes from the Marshall Islands ( Reish 1968). He made two field trips to the islands and a compilation of all recorded species, and his objective was very important because he tried to prepare a reference collection for the marine lab there (now the Mid-Pacific Marine Lab, University of Hawaii). The species-group name is a noun in the genitive case ( ICZN 1999, Art. 31.1.2).

Variation. The paratype ( Fig. 37A, B View FIGURE 37 ) has an unusual development of the nuchal organs, because they are completely exposed and projected posteriorly, which differs from the holotype and other additional specimens ( Fig. 37D, E View FIGURE 37 ) where the nuchal organs are barely projected posteriorly. Parapodial features do not differ at all ( Fig. 37C, F View FIGURE 37 ), as well as other prostomial sensors like palps, antennae and eyes. This explains why they are regarded as conspecific despite the difference in the development of the nuchal organs lobes. An alternative would be to regard this species as belonging in Paradalhousia n. gen. but its species have very large eyes and notochaetae are usually abundant, and these features are not present in the paratype.

Remarks. Leocrates reishi n. sp. belongs in the group having small eyes, with anterior eyes twice larger than posterior ones, together with L. ahlfeldae n. sp. from India, L. chinensis Kinberg, 1866 from Hong Kong, and L. giardi Gravier, 1900 from the Red Sea. However, L. reishi is the only species with notacicular lobes blunt (all others have tapered lobes), and with scarce neurochaetae, 15–20 per bundle; L. giardi has scarce neurochaetae but its notacicular lobes are tapered.

Distribution. Marshall Islands, the Philippines, New Caledonia and the French Polynesia, in coralline substrates, in 1–2 m depth.

Kingdom

Animalia

Phylum

Annelida

Class

Polychaeta

Order

Phyllodocida

Family

Hesionidae

Genus

Leocrates

Loc

Leocrates reishi

Salazar-Vallejo, Sergio I. 2020
2020
Loc

Leocrates chinensis: Hartman 1954: 622

Bailey-Brock, J. H. & Hartman, O. 1987: 262
Pettibone, M. H. 1970: 215
Reish, D. J. 1968: 213
Hartman, O. 1954: 622
1954
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