Enoplometopus gracilipes (de Saint Laurent, 1988 )

Poupin, Joseph, 2003, Reef lobsters Enoplometopus A. Milne Edwards, 1862 from French Polynesia, with a brief revision of the genus (Crustacea, Decapoda, Enoplometopidae), Zoosystema 25 (4), pp. 643-664 : 646-657

publication ID

https://doi.org/ 10.5281/zenodo.4525031

persistent identifier

https://treatment.plazi.org/id/0396AD3E-FFE4-DC7B-FC86-FA4FFC395ECE

treatment provided by

Felipe

scientific name

Enoplometopus gracilipes (de Saint Laurent, 1988 )
status

 

Enoplometopus gracilipes (de Saint Laurent, 1988) View in CoL

( Figs 4 View FIG ; 5 View FIG ) Hoplometopus gracilipes de Saint Laurent, 1988: 62 (type locality: Moruroa atoll, Tuamotu; paratype from Loyalty Islands).

Hoplometopus gracilipes – Poupin et al. 1990: 16 ( French Polynesia). — Poupin & Richer de Forges 1991: 211 ( French Polynesia). — Poupin 1996a: 14 ( French Polynesia); 1996b: 95 (checklist).

Enoplometopus gracilipes View in CoL – Chan 1998: 998 (western Pacific). — Chan & Yu 1998: 190 (key).

? Enoplometopus gracilipes View in CoL (provisional determination according to illustration only; see Remarks) – Anonymous 1973: unnumbered plate ( Japan). — Miyake 1983: 106 ( Japan).

MATERIAL EXAMINED. — French Polynesia. Australs Islands , Rurutu, Frv Marara , stn 147, 22°27.3’S, 151°23.1’W, trap 280 m, 9.III.1989, 5 ƋƋ cl 52- 60 mm, bl 161-182 mm, 2 ♀♀ cl 50-54 mm, bl 154-160 mm ( MNHN As 548, in two vials) GoogleMaps ; stn 423, 22°29.3’S, 151°21.6’W, trap 80 m, 10.VIII.1991, 1 Ƌ cl 40 mm, bl 117 mm, 1 ♀ cl 42 mm, bl 121 mm ( MNHN As 626). — Tuamotu Islands , Moruroa, Frv Marara , stn unknown, trap 250-300 m, 1987, 1 Ƌ holotype cl 53 mm, bl 160 mm ( MNHN As 544) GoogleMaps ; Frv Marara , stn 210, 21°46.9’S, 138°55.4’W, trap 210 m, 30.XI.1989, 3 ƋƋ cl 46-53 mm, bl 139-159 mm ( MNHN As 622) GoogleMaps ; stn 207, 21°46.8’S, 138°52.1’W, trap 200 m, 28.XI.1989, 1 Ƌ cl 43 mm, bl 134 mm ( MNHN As 623) GoogleMaps .

New Caledonia. Loyalty Islands, stn PR1-R3, trap 200 m, VI.1977, coll. A. Intès, 1 Ƌ paratype cl 44 mm, bl 133 mm ( MNHN As 531).

DISTRIBUTION. — West and central Pacific:? Japan, New Caledonia (Loyalty Islands), French Polynesia ( Austral Islands : Rimatara , Rurutu , Tubai ; Society Islands : Bora Bora , Tahiti , Tupaï ; Tuamotu Islands : Fangataufa , Moruroa ). Depths : 80-300 m, usually deeper than 100 m. On hard bottoms .

DESCRIPTION

Rostrum slightly overreaching spine of scaphocerite, triangular in dorsal view, dorsally depressed, with four spines on lateral margin. Carapace bearing fine tomentum on gastric area, armed with five median, two postcervical, one intermediate, one supraocular, and three lateral spines; lateral face with one branchiostegal plus two to four additional small spines ( Fig. 5A View FIG ).

Antennular peduncle with basal segment as long as median and distal segments together; distal segment with two terminal flagella, inner longer than outer. Basal segment of antennal peduncle with antennal gland on ventral face and seven or eight spines on anterior margin, inner and outer ones large; second segment with one distolateral spine; third segment with rounded distal process armed with one subdistal spine (occasionally missing); fourth and fifth segments subequal and unarmed; flagellum long, overreaching tip of chelipeds. Outer margin of antennal scaphocerite straight with one strong distal spine; inner margin distally curved, furnished with plumose setae; upper face with deep groove, parallel to outer margin.

Third maxilliped almost reaching to distal margin of carpus of cheliped. Basis with one distoventral spine. Ischium triangular in cross section, with one strong distodorsal spine; ventral outer margin furnished with long setae and armed with one or two distal spines; ventral inner margin with comblike crista dentata made of about 20 spines of irregular size; merus triangular in cross section, with one distodorsal spine; ventral outer margin with three to six spines on distal two thirds, increasing in size anteriorly; ventral inner margin with setae. Carpus with one distolateral spine. Propodus and dactyl with ventral faces flattened, bearing long setae on margins.

Cheliped much longer than ambulatory legs. Ischium compressed, with one distodorsal spine; ventral margin with five to seven spines, increasing in size anteriorly. Merus compressed; dorsal margin with main row of six or seven spines and short row of two or three outer spines, distally; anterior margin with two dorsal spines, one spine on inner and outer articular condyles, and one ventral spine; ventral face with eight or nine spines on outer margin and six or seven spines on inner margin; Carpus with four spines on dorsal face; anterior margin with four dorsal spines, one or two small outer spines, one strong inner spine and one strong ventral spine. Chela very long, 5.6-7.6 times as long as wide (average 6.5); palm ovate in cross section, smooth on upper and lower faces; outer margin with nine to 12 spines; inner margin with six to nine spines. Fingers long and slender, 0.5 times as long as chela, with sharp, inwardly curved tips; cutting edges straight, with six to eight main teeth and minute denticulation in between; outer margins unarm- ed, with few sparse setae ( Fig. 5C View FIG ).

Second pereopod slender, subchelate, reaching to proximal fourth of chela, rounded in cross section; upper and lower margins with few long setae. Merus with one distolateral spine. Carpus 0.4 times as long as merus, armed with one distoventral spine. Propodus as long as merus, with distoventral process bearing five to eight tiny spines on upper margin, and two mobile spines distally. Dactyl short, 0.20 times as long as propodus, terminated by strong distal claw; lower margin armed with 25-30 tiny spines plus two subdistal corneous spines; distodorsal margin with one mobile spine; distal outer face with one mobile spine ( Fig. 5D View FIG ). Third pereopod with one distoventral spine on merus. Carpus unarmed. Propodus with distoventral process reduced, bearing two or three tiny spines on dorsal margin and two mobile spines distally. Dactyl with strong terminal claw, three or four mobile spines disposed on outer and inner faces; ventral margin with 10-13 tiny spines and one corneous spine distally. Fourth pereopod similar to P3; distoventral process of propodus reduced, with three or four mobile spines distally. Pereopod 5 shortest, without terminal pincer. Merus and carpus without spines. Propodus with six to eight small spines at distoventral angle. Dactyl with five or six mobile spines disposed on inner and outer faces; proximal half with ventral process armed with row of minute spines.

Thoracic sternite V of male with two anterior and two posterior spines; lateral margin with zero or one spine. Sternite VI with two anterior and two posterior spines; anterolateral margin with three to six tubercles or spines; posterolateral margin with zero or one spine. Sternite VII as a deep V-shaped hollow, with two anterior spines or granules and two stronger posterior spines, forwardly curved; anterolateral margin with three or four spines or tubercles; posterolateral margin with one or two spines or tubercles. In female, seminal receptacle on sternite VII with median slit covered by transverse setae.

Abdomen smooth, with few long setae on tergites V-VI. Pleuron of abdominal somite I narrow, overlapped by pleuron of somite II. Pleura of somites II-V with sharp tooth, posteriorly curved ( Fig. 5B View FIG ). Pleuron of somite VI with blunt tooth. Posterior margin of tergite VI unarmed ( Fig. 5E View FIG ). Male first pleopod as an uniramous rigid blade, indented distally as illustrated on Figure 5E View FIG . Second pleopod biramous; endopod with two appendices (interna and masculina). Pleopods 3-5 biramous; endopod and exopod leaflike, furnished with long setae on margins. Female first pleopod uniramous, long and slender. Pleopods 2-5 biramous; endopod and exopod similar to male pleopods 3-5, except for rounded basal process furnished with few long setae on inner margin of endopod.

Basal segment of uropod segment with two dorsal spines and one ventral spine on distal margin; endopod with one distolateral spine; exopod with spiny diaeresis on distal fourth; lateral edge of diaeresis with one dorsal fixed spine and one ventral mobile spine. Telson subrectangular, slightly longer than wide; lateral margin with two spines of similar size; distolateral angle with two spines, inner one longer ( Fig. 5E View FIG ).

Coloration ( Fig. 4 View FIG )

Ground color of body pale orange with tip of spines white. Carapace, abdomen, and telson with numerous dark orange patches, grouped by sets of two to four. Cheliped pale orange with faint darker bands. Ambulatory legs with alternat- ed white and orange bands.

REMARKS

In 16 specimens examined a few unusual armaments have been observed. The lateral margin of rostrum can have three to five spines, instead of the usual four. There are two intermediate spines on the carapace, instead of one, in a female cl 42 mm ( MNHN As 626). The distoventral spine of carpus of second pereopod was absent on the smallest specimen examined (male cl 40 mm). Spines were also occasionally missing on inner and outer faces of dactyls of ambulatory legs.

Enoplometopus gracilipes is morphologically related to E. holthuisi Gordon, 1968 and E. voigtmanni Türkay, 1989 . The three species have in common the same disposition of spines on the carapace, a similar shape of pleura of abdominal somites II-V, and a similar long and slender chela, smooth on the upper and lower faces of palm, with fingers as long as the palm. Enoplometopus gracilipes is at once distinguished from the two other species by its coloration, being the only one with spots on the carapace whereas the lateral face of the carapace has a large white circle in E. holthuisi , and a network of streaks in E. voigtmanni . In the absence of coloration E. gracilipes can be distinguished by examination of the posterior margin of the sixth abdominal tergite, which has no spines, while it has two short lateral spines in the two other species (cf. Fig. 5E View FIG with Fig. 7E View FIG ). Although shape of male first pleopod is still not known in E. voigtmanni , it is also obviously different between E. gracilipes and E. holthuisi (cf. Fig. 5F View FIG with Fig. 7F View FIG ). Finally, E. gracilipes is a deep-water species, mostly collected at depths greater than 100 m, while E. holthuisi and E. voigtmanni are only known at depths less than 100 m.

Illustrations of an undetermined specimen have been published in two Japanese books ( Anonymous 1973; Miyake 1983). According to its coloration, this unique specimen could reasonably belong to E. gracilipes . However, this provisional determination must be confirmed when more specimens are available from Japan.

Enoplometopus holthuisi Gordon, 1968 ( Figs 6 View FIG ; 7 View FIG )

Enoplometopus holthuisi Gordon, 1968: 90 View in CoL (type locality: Banda Islands, Moluccas, Indonesia).

Enoplometopus holthuisi View in CoL – Intès & Le Loeuff 1970: 1442 (text). — Burukovsky 1983: 153 (key). — Daum 1982: 265 ( Philippines; pro parte, only illustration p. 265). — Türkay 1989: 228 (Hawaii). — Bonvallot et al. 1994: 144 (Tuamotu). — Poupin 1996b: 8 (checklist). — Chan 1998: 998, 1000 (western Pacific). — Chan & Yu 1998: 189 (key). — Debelius 1999: 204 (Hawaii).

Enoplometopus (Hoplometopus) holthuisi View in CoL – Holthuis 1983: 297 ( Marshall Islands; Hawaii).

Hoplometopus holthuisi View in CoL – de Saint Laurent 1988: 61 (list). — Gosliner et al. 1996: 220 (Hawaii). — Hoover 1998: 241 (Hawaii).

Enoplometopus antillensis View in CoL – Holthuis 1946: 79 ( Moluccas) (non Enoplometopus antillensis Lütken, 1865 View in CoL , except for pl. V, fig. h and pl. VII, fig. b, drawn from type specimen of E. antillensis View in CoL ).

Enoplometopus occidentalis View in CoL – George & George 1979: 78 (photograph) (non Enoplometopus occidentalis ( Randall, 1840)) View in CoL .

Hoplometopus sp. nov. – Poupin 1996a: 14 ( French Polynesia) (non sp. nov. = E. holthuisi , see Remarks).

Non Enoplometopus holthuisi View in CoL – Daum 1982: 266 (illustrated specimen belongs to E. voigtmanni View in CoL ). — Allen & Steene 1994: 145 (photograph = E. voigtmanni View in CoL ).

MATERIAL EXAMINED. — French Polynesia. Austral Islands, Rurutu, Frv Marara , stn 423, 22°29.3’S, 151°21.6’W, trap 80 m, 10.VIII.1991, 1 Ƌ cl 28 mm, bl 96 mm ( MNHN As 624). — Society Islands, Tahiti, dry remains of chelae only with this label “ Hoplometopus gordonae sp. nov. ” ( MNHN As 625).

Indonesia. Banda Islands, V.1921, leg. E. Van der Velde, 1 ♀ holotype cl 33 mm, bl 105 mm, 1 Ƌ paratype cl 30 mm, bl 93 mm ( ZMA De 101.265).

La Réunion. 1973, coll. Y. Plessis, 1 Ƌ cl 22.5 mm, bl 74.5 mm ( MNHN As 271).

DISTRIBUTION. — West Indian Ocean to central Pacific : La Réunion, Indonesia ( Banda Islands , Moluccas), Philippines, Marshall Islands ( Enawetak atoll), Hawaii , French Polynesia ( Austral Islands : Rurutu ; Society Islands : Tahiti ; Tuamotu Islands). Depths: 20-80 m. On hard bottoms .

SHORT DESCRIPTION

(SPECIMEN FROM FRENCH POLYNESIA)

Rostrum with three spines on lateral margin. Carapace with five median, two postcervical, one intermediate, one supraocular, and three lateral

spines ( Fig. 7A View FIG ). Chela 4.6 times as long as wide, palm ovate in cross section ( Fig. 7C View FIG ). Upper and lower faces of palm smooth; outer margin with eight spines; inner margin with two rows of five spines, converging distally. Fingers 0.4 times as long as chela, with sharp inward curved crossing tips; cutting edges denticulated with five or six larger teeth; outer edges smooth, furnished with very long setae extending well beyond tip of fingers (see Remarks).

Second pereopod circular in cross section, reaching to proximal third of chela. Merus and carpus with distoventral spine. Propodus subequal to merus, furnished with few long setae; distoventral angle with process armed with five to eight tiny spines on upper margin, and two mobile spines, distally ( Fig. 7D View FIG ). Dactyl short, 0.2 times as long as propodus. Pereopod 3 and 4 shorter than P2, with terminal pincers reduced. Pereopod 5 is the shortest and has no terminal pincer.

Pleura of abdominal somites II-V, each with sharp, posteriorly curved tooth; pleuron of somite VI with blunt tooth ( Fig. 7B View FIG ). Posterior margin of tergite VI with three median tubercles flanked by two short spines ( Fig. 7E View FIG ). Male first pleopod subrectangular with deep incision on distal margin ( Fig. 7F View FIG ). Telson with two lateral spines of similar size and two distolateral spines, inner one longer ( Fig. 7E View FIG ).

Coloration ( Fig. 6 View FIG )

Ground color of body orange with white at tip of spines. Lateral face of carapace with large white circle, on distal half, and wavy white lines on proximal half. Abdominal somites with white spots bordered by dark orange rings, as illustrated on Figure 6 View FIG . Chela orange with faint reticulated lines on palm, and alternated dark and light orange bands on fingers. Ambulatory legs banded in white and orange on whole length.

REMARKS

Because of the particular shape of its chela that is distinct from typical E. holthuisi , the specimen trapped around the French Polynesian islands had been previously attributed to a new species ( Poupin 1996a). In this work it has been compar- ed carefully with the holotype of E. holthuisi , which confirms the distinctive shape of its chela (cf. Fig. 7C View FIG with Fig. 7G View FIG ). It is less elongated, being 4.6 times as long as wide, vs 6.4 in holotype, and has shorter fingers, 0.4 times as long as chela, instead of 0.5 in holotype. Outer edges of the fingers are also furnished with very long setae ( Fig. 6B View FIG ), absent on the holotype and never observed on photographs of E. holthuisi consulted during this study. Despite these obvious differences, all other characters of the Polynesian specimen are those of E. holthuisi , particularly the shape of male first pleopod, a very distinctive character in this species. It thus seems that the peculiar shape of its chela must be attributed to its small size.

Enoplometopus holthuisi is related to E. voigtmanni . As denoted in the Remarks of E. gracilipes , the two species are easily separated by their coloration, in particular the lateral face of the carapace which has a large white circle, in E. holthuisi , and a network of streaks, in E. voigtmanni . They also differ by the shape of the spines on the abdominal pleura II-V, as illustrated in Türkay (1989: figs 1, 2b). When male first pleopod is known in E. voigtmanni it will be interesting to check if the two species can also be separated by the shape of this appendage. Enoplometopus holthuisi is also related to E. gracilipes , and the differences between the two species have been listed under E. gracilipes . It is interesting to point out that the single specimen of E. holthuisi caught during the fishing operations of the Frv Marara (stn 423, 80 m) was associated in the trap with E. gracilipes . Enoplometopus holthuisi is usually reported in shallow waters, between 20-50 m, while E. gracilipes is mostly caught at depths greater than 100 m. Therefore, it appears that these two species can co-occur at intermediate depths, between 50- 100 m.

SPECIES IN MNHN COLLECTIONS

Enoplometopus antillensis Lütken, 1865 View in CoL Enoplometopus antillensis Lütken, 1865: 265 View in CoL (type locality: West Indies).

Enoplometopus antillensis View in CoL – Holthuis 1946: 72 (type specimen). — Fausto Filho 1970: 55 ( Brazil); 1976: 222 ( Brazil). — Debelius 1986: 13 (photograph). — Wirtz et al. 1988: 170 ( Cape Verde). — Manning & Camp 1989: 412 ( Bermuda, East coast of Florida, Bahama, Panama, Netherlands West Indies, St Helena Island, Gulf of Guinea). — Scelzo & Rodriguez 1991: 226 ( Venezuela). — González Pérez 1995: 134, 137 (Canary Islands). — Wirtz & Herrera 1995: 116 (Canary Islands). — Wirtz 1996: 368 (Canary Islands). — Chan & Yu 1998: 190 (key). — Debelius 1999: 45 (Canary Islands).

Enoplometopus (Hoplometopus) antillensis View in CoL – Holthuis 1983: 282 (new subgenus).

Hoplometopus antillensis View in CoL – de Saint Laurent 1988: 61 (list).

Enoplometopus dentatus Miers, 1880: 381 (St Helena) View in CoL . — Gordon 1968: 80 (St Helena). — Manning & Camp 1989: 412 (West Indies; St Helena).

Enoplometopus View in CoL sp. – Forest 1959: 22 (Gulf of Guinea). Non Enoplometopus antillensis View in CoL – Holthuis 1946: 79 (= E. holthuisi Gordon, 1968 View in CoL , except for pl. V, fig. h and pl. VII, fig. b, drawn from type specimen of E. antillensis View in CoL ). A few additional references can be found in Manning & Camp (1989) and González Pérez (1995).

MATERIAL EXAMINED. — West Atlantic. Guadeloupe, Basse Terre, îlet du Gosier, trap 80 m, XI.2002, coll. D. Lamy, A. Crosnier det., 1 Ƌ cl 37 mm, bl 97 mm ( MNHN As 629).

Central Atlantic. Ascencion Island, off Southwest Point near Rocked Launcher, under rocks, dive at night 12 m, V.1981, coll. McDowell, 1 Ƌ cl 26.7 mm, bl 81.5 mm ( MNHN As 558, leg. R. B. Manning).

East Atlantic. Gulf of Guinea, Annobon Island, Frv Calypso , stn 109, 1°25.10’S, 5°36.10’E, dive at 20 m, 5.VII.1956, 1 ♀ cl 20.0 mm, bl 62 mm (MNHN As 557).

DISTRIBUTION. — West Atlantic: Bermuda, east coast of Florida, Bahama (Grand Bahama Island), Netherlands West Indies ( Bonaire), French West Indies (Guadeloupe), Panama (Golfo de Mesquites, Bahía de Almirante), Venezuela, Brazil (off northeast coast and off Rio Grande do Norte State). Central Atlantic: Ascencion and St Helena islands, off Brazil 03°17’S, 29°57’W (larvae). East Atlantic: Madeira, Canary Islands (Gran Canaria, Hierro, Lanzarote, Tenerife), Gulf of Guinea (off Gabon and Annobon Island), Cape Verde (Sal). Deep distribution: 5- 201 m, mainly between 15- 30 m. On rocky bottoms.

DIAGNOSIS. — Lateral margin of rostrum with three or four spines. Carapace armed with five median, two postcervical, one intermediate, one supraocular, and three lateral spines. Chela broad and compressed, 3.6- 4.0 times as long as wide, upper and lower faces of palm smooth; outer margin of dactyl smooth. Second pereopod with dactyl 0.3 times as long as propodus; carpus and merus with distoventral spine. Pleura of abdominal somites II-V with smooth margins and sharp, posteriorly curved, median tooth. Male first pleopod with deep incision on distal margin. Telson with two lateral and two distolateral spines.

COLORATION

Ground color of body orange to red with white on spines. Lateral face of carapace with large white circle, surrounding median white spot, and white oblique lines posterior to circle; dorsal and posterolateral faces with minute red spots on lighter red background. Upper face of palm of chela with several orange red patches; fingers banded in white and orange red. Abdomen with white spots circled in dark orange or black. Ambulatory legs red orange with narrow white bands ( González Pérez 1995).

REMARKS

This is the most common species found in the Atlantic and the only Enoplometopus lobster report- ed from the tropical west Atlantic. In the tropical east Atlantic it co-occurs with E. callistus . In central Atlantic Islands, St Helena and Ascencion islands, it must be very common as the collector of the specimens examined herein indicates on the label: “[...] specimens from St Helena are larger and are often eaten there, mostly by fishermen as they get into their fish and lobster traps”.

Enoplometopus callistus Intès & Le Loeuff, 1970 View in CoL ( Fig. 8 View FIG )

Enoplometopus callistus Intès & Le Loeuff, 1970: 1442 View in CoL

(type locality: Gulf of Guinea, Ghana, off Takoradi).

Enoplometopus (Hoplometopus) callistus – Holthuis

1983: 282 (new subgenus).

Enoplometopus callistus View in CoL – González Pérez 1995: 136

(Canary Islands). — Wirtz & Herrera 1995: 116

(Canary Islands). — Wirtz 1996: 368 (Canary Islands;

20-200 m). — Chan & Yu 1998: 190 (key). —

Debelius 1999: 44 (Canary Islands).

Enoplometopus biafri Burukovsky, 1972: 180 View in CoL

( Nigeria). — Burukovsky 1983: 153 (key). —

Holthuis 1983: 281 (synonymy).

Hoplometopus callistus View in CoL – de Saint Laurent 1988: 61 (list).

Some additional references can be found in González Pérez (1995).

MATERIAL EXAMINED. — East Atlantic. Gulf of Guinea: Ghana, off Takoradi, c. 5°30’N, 2°W, trawl 48 m, V.1968, coll. fishermen, 1 Ƌ cl 42 mm, bl 128 mm (holotype, MNHN As 51). —?Market, 18.XII.1967, 1 Ƌ cl 45 mm, bl 140 mm, 1 ♀ cl 53.5 mm, bl 153 mm ( MNHN As 627).

DISTRIBUTION. — East Atlantic : Gulf of Guinea (off Ghana, off Nigeria) ; Canary Islands (Gran Canaria, La Palma, Tenerife). Deep distribution: 30-200 m. On hard bottoms .

DIAGNOSIS. — Lateral margin of rostrum with three or four spines. Carapace with five median, one postcervical, one intermediate, one supraocular, and two lateral spines. Chela broad and compressed, 2.6-3.9 times as long as wide, upper and lower faces of palm smooth; outer margin of dactyl with nine or 10 spines disposed over entire length (see Remarks). Dactyl of second pereopod 0.3 times as long as propodus. Pleura of abdominal somites II-V finely denticulated and with sharp median tooth ( Fig. 8B View FIG ). Distal margin of male first pleopod with small denticulations, as illustrated on Figure 8C View FIG , without deep indentation. Telson with two lateral and two distolateral spines.

COLORATION

Carapace, abdomen and chelae pale orange with large orange red patches. Antennae white. Ambulatory legs orange with narrow white bands ( González Pérez 1995; Wirtz 1996).

REMARKS

The arrangement of spines on the carapace, as indicated herein, differs slightly from the original description by Intès & Le Loeuf (1970). These authors indicate four median plus two postcervical spines, instead of five median plus one postcervical spine in this work. This is because they have considered as “postcervical” the posteriormost median spine that is in fact situated on the cervical groove, as observed also in E. crosnieri .

The arrangement of spines on the outer margin of dactyl of chela was first used by Bouvier (1915) who distinguished two states: 1) two to three spines disposed at tip only; or 2) spines disposed over the full length. Although state 2) clearly applies here for the type of E. callistus , it has been observed that spines on the proximal two thirds are reduced to spiny scales in the two larger specimens examined (MNHN As 627), a variation that could be a source of misidentification if not taken into account (cf. Fig. 8A View FIG and Fig. 8D View FIG ).

Marginal denticulation of pleura II-V is a new diagnositic character for the genus. It has also been observed in a juvenile of E. holthuisi (Ƌ cl 22.5 MNHN As 271) which has tiny denticles on pleura II-III only, and is also illustrated for a juvenile of E. antillensis in Manning & Camp (1989: 415 , fig. 4D). Therefore, it seems to be a juvenile character that is retained in the adult stage of E. callistus .

MNHN

Museum National d'Histoire Naturelle

ZMA

Universiteit van Amsterdam, Zoologisch Museum

Kingdom

Animalia

Phylum

Arthropoda

Class

Malacostraca

Order

Decapoda

Family

Enoplometopidae

Genus

Enoplometopus

Loc

Enoplometopus gracilipes (de Saint Laurent, 1988 )

Poupin, Joseph 2003
2003
Loc

Enoplometopus gracilipes

CHAN T. Y. & YU H. P. 1998: 190
1998
Loc

Hoplometopus

POUPIN J. 1996: 14
1996
Loc

Enoplometopus callistus

GONZALEZ PEREZ J. A. 1995: 136
1995
Loc

Hoplometopus gracilipes

POUPIN J. 1996: 14
POUPIN J. & RICHER DE FORGES B. 1991: 211
POUPIN J. & TAMARII T. & VANDENBOOMGAERDE A. 1990: 16
1990
Loc

Hoplometopus holthuisi

HOOVER J. 1998: 241
GOSLINER T. M. & BEHRENS D. W. & WILLIAMS G. C. 1996: 220
SAINT LAURENT M. & DE 1988: 61
1988
Loc

Hoplometopus antillensis

SAINT LAURENT M. & DE 1988: 61
1988
Loc

Hoplometopus callistus

SAINT LAURENT M. & DE 1988: 61
1988
Loc

Enoplometopus gracilipes

MIYAKE S. 1983: 106
1983
Loc

Enoplometopus (Hoplometopus) holthuisi

HOLTHUIS L. B. 1983: 297
1983
Loc

Enoplometopus (Hoplometopus) antillensis

HOLTHUIS L. B. 1983: 282
1983
Loc

Enoplometopus holthuisi

ALLEN G. R. & STEENE R. 1994: 145
DAUM W. 1982: 266
1982
Loc

GEORGE J. D. & GEORGE J. J. 1979: 78
1979
Loc

Enoplometopus biafri

BURUKOVSKY R. 1972: 180
1972
Loc

Enoplometopus holthuisi

DEBELIUS H. 1999: 204
CHAN T. Y. & YU H. P. 1998: 189
POUPIN J. 1996: 8
BONVALLOT J. & LABOUTE P. & ROUGERIE F. & VIGNERON E. 1994: 144
TURKAY M. 1989: 228
BURUKOVSKY R. 1983: 153
DAUM W. 1982: 265
INTES A. & LE LOEUFF P. 1970: 1442
1970
Loc

Enoplometopus callistus Intès & Le Loeuff, 1970: 1442

INTES A. & LE LOEUFF P. 1970: 1442
1970
Loc

Enoplometopus holthuisi

GORDON I. 1968: 90
1968
Loc

Enoplometopus antillensis

HOLTHUIS L. B. 1946: 79
1946
Loc

Enoplometopus antillensis

DEBELIUS H. 1999: 45
CHAN T. Y. & YU H. P. 1998: 190
WIRTZ P. 1996: 368
GONZALEZ PEREZ J. A. 1995: 134
WIRTZ P. & HERRERA R. 1995: 116
SCELZO M. A. & RODRIGUEZ G. 1991: 226
MANNING R. B. & CAMP D. K. 1989: 412
WIRTZ P. & MULLER B. & NAHKE P. 1988: 170
DEBELIUS H. 1986: 13
FAUSTO FILHO J. 1970: 55
HOLTHUIS L. B. 1946: 72
1946
Loc

Enoplometopus dentatus

MANNING R. B. & CAMP D. K. 1989: 412
GORDON I. 1968: 80
MIERS E. J. 1880: 381
1880
Loc

Enoplometopus antillensis Lütken, 1865

LUTKEN C. 1865: 265
1865
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