Micropagurus polynesiensis ( Nobili, 1906 )
publication ID |
https://doi.org/ 10.11646/zootaxa.1090.1.1 |
publication LSID |
lsid:zoobank.org:pub:172D3D3A-0929-48AB-9BDE-A81674FD854C |
persistent identifier |
https://treatment.plazi.org/id/03C687CF-2E53-FFE6-FECA-FB70FC63BA28 |
treatment provided by |
Felipe |
scientific name |
Micropagurus polynesiensis ( Nobili, 1906 ) |
status |
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Micropagurus polynesiensis ( Nobili, 1906) View in CoL ( Figs. 14–18 View FIGURE 14 View FIGURE 15 View FIGURE 16 View FIGURE 17 View FIGURE 18 , 19A–C View FIGURE 19 , 20 View FIGURE 20 )
Anapagurus polynesiensis Nobili, 1906: 260 View in CoL ; 1907: 372, pl. 1: fig. 10.— Forest, 1956: 1056.— Chevalier et al., 1968: 119.
Micropagurus polynesiensis View in CoL .— Haig & Ball, 1988: 184.— Poupin, 1996: 18, 78 (checklist).
Micropagurus vexatus Haig & Ball, 1988: 181 View in CoL , figs 11, 12.
Material Examined. Syntypes: 1♂, SL = 1.5 mm, 2♀, SL = 1.2 mm (1 female damaged, not measured), Rikitea, French Polynesia, coll. M. Seurat, MNHNPg 2765. Other material: PACIFIC OCEAN: Loyalty Islands: 1♀, SL = 1.8 mm, stn. 1452, 2 25 m, between Cape Mandé and Cape Lefèvre (=Nem), Santal Bay, Lifou Island, 20°54.6'S, 167°02.1' E, 20, 22 Nov. 2000, LIFOU, MNHNPg 7251; 2♂, SL = 1.2, 1.8 mm, 1 ov. ♀, SL = 2.0 mm, stn. 1453, 21– 30 m, on gorgonians, underwater cliff, between Cape Mandé and Cape Lefèvre (=Nem), Santal Bay, Lifou Island, 20°54.6'S, 167°02.1' E, 22 Nov. 2000, MNHNPg 7252; 1♂, SL = 1.0 mm, stn. 1455, 15– 20 m, underwater cliff, between Cape Wekutr and Cape Wajez, Santal Bay, Lifou Island, 20°56.8'S, 167°02.7' E, 25 Nov. 2000, LIFOU, MNHNPg 7253; 1♂, SL = 2.0 mm, stn. 1419, 5 m, mud with fragments and algae, Gaatcha Bay, Santal Bay, Lifou Island, 20°55.6'S, 167°04.5' E, 10 Nov. 2000, LIFOU, MNHNPg 7248; 2♂, SL = 0.8, 1.2 mm, 2♀, SL = 1.1, 1.1 mm, stn. 1449, 17 m, north of Cape Aimé Martin (= Acadro), Santal Bay, Lifou Island, 20°45.8'S, 167°01.65' E, 17 Nov. 2000, LIFOU, MNHNPg 7249; 1♀, SL = 1.6 mm, stn. 1450, 27 31 m, north of Cape Aimé Martin (= Acadro), Santal Bay, Lifou Island, 20°45.8'S, 167°01.65' E, 1721 Nov. 2000, LIFOU, MNHNPg 7250; 1 ov. ♀, SL = 1.7 mm, stn. 1456, 25 30 m, underwater cliff, in region of Cila, north east of Santal Bay, Lifou Island, 20°49.3'S, 167°10.4' E, 26 Nov. 2000, LIFOU, MNHNPg 7254; 1♀, SL = 1.7 mm, st. 1221, 10 m, d'Ouvéa Lagoon, 20°28.9'S, 166°31.0' E, coll. R. Leborge, 11 Sept. 1992, Campagne PLOUVEAL, MNHNPg 7247. New Caledonia: 1♂, SL = 1.0 mm, 10 m, Touho, 8 Sept. 1993, MNHN Pg 7255; 1♂, SL = 1.6 m, Touho, 6 Sept. 1993, MNHNPg 7256; 2 ov. ♀, SL = 1.6, 1.6 mm, 57 m, TouhoTié (ToumoTié on the label), MNHNPg 7257; 1♂, SL = 2.1 mm, st. 395, 31 m, Grand Récif Sud, 22°48'S, 167°08' E, coll. B. Richer ( ORSTOM), 23 Jan. 1985, LAGON, MNHNPg 7258; 1♂, SL = 2.4 mm, st. 464, 44 m, Surprise Atoll, 18°21'S, 163°03'E, B. Richer ( ORSTOM), 1 Mar. 1985, LAGON, MNHNPg 7259; 1 ov. ♀, SL = 1.2 mm, 1♂, SL = 1.4 mm, 2030 m, lagoon, Grotte Merlet, coll. J. L. Menou, 1921 Jan. 1993, MNHNPg 7260. Tahiti: 1♀, SL = 0.7 mm, Tiahurá, coll. B. Thomassium, MNHNPg. 3404. Philippine Islands: 1♂, SL = 1.7 mm, coll. by diving, 17 Dec. 1980, MNHNPg. 2766. Japan: 1♂, SL = 1.6 mm, diving, coll. Tetsuya Kinjyou, Okinawahontow, Ryukyus, Feb. 2004, CBMZC 8380. INDIAN OCEAN: Indonesia: 1♂, SL = 1.6 mm, Banda stn. 9, Alpha Helix Expedition, LACMAHF 755 (= paratype of Micropagurus vexatus ); 1 ov. ♀, SL = 1.1 mm, Siboga st. 144, 45 m, coral bottom and Lithothamnion , dredge, Salomakiée (Damar) Island, 1°S, 127°E, 79 Aug. 1899, MNHN Pg 7278. Seychelles: 1♀, SL = 1.8 mm, st. 4, 32 m, hard bottom, 5°07.7'S, 56°34.0'E, 2 Sept. 1980, Campagne REVES II, coll. R. Cleva, MNHNPg 7261; 1♂, SL = 1.3 mm, st. 7, 50 55 m, fine sand and algae Halimeda , 4°51.8'S, 55°59.6'E, 3 Sept. 1980, Campagne REVES II, coll. R. Cleva, MNHNPg 7262.
Description. Shield ( Fig. 14A, B View FIGURE 14 ) approximately as long as broad; anterior margin between rostral lobe and lateral projections weakly concave; posterior margin rounded or roundly truncate; dorsal surface with rows or tufts of moderately long setae. Rostral lobe slightly produced, broadly rounded. Lateral projections broadly rounded, unarmed.
Ocular peduncles ( Fig. 14A, B View FIGURE 14 ) 0.9–1.0 length of shield; slightly to strongly inflated basally, slightly inflated distally; surfaces sometimes with several low protuberances accompanied distally by few short setae. Corneas dilated. Paired interocular lobes prominent. Ocular acicles each bearing 4–7 spines on distal margin and fringe of setae just proximal to spine row.
Antennular peduncles ( Fig. 14A, B View FIGURE 14 ) shorter than or barely reaching to bases of corneas; ultimate and penultimate segments unarmed; basal segment with strong spine at ventrolateral distal angle.
Antennal peduncles ( Fig. 14A, B, C View FIGURE 14 ) not reaching to bases of corneas; fifth and fourth segments unarmed; third segment with sharp spine at ventrodistal margin; second segment with dorsolateral distal angle produced, terminating in simple or bifid spine; dorsomesial distal angle with small spine; first segment with small, simple or bifid spine on lateral margin distally and acute spine ventrodistally. Antennal acicles moderately short, each terminating in small spine; mesial margin unarmed or with 1 or 2 small spines or tubercles; lateral margin with spine proximally or unarmed.
Third maxilliped with basis bearing 1 or 2 small teeth; ischium with moderately developed crista dentata and accessory tooth; merus and carpus each bearing strong dorsodistal spine.
Right cheliped stout; male cheliped ( Fig. 15 View FIGURE 15 ) much stouter but armature much weaker than female ( Fig. 16 View FIGURE 16 ). Dactyl 0.4–0.6 (male) or 0.7–0.8 (female) length of palm, terminating in small corneous claw not visible in dorsal view; cutting edge ( Fig. 15D View FIGURE 15 ) with 2 calcareous teeth proximally and row of tiny corneous and calcareous teeth distally; dorsomesial margin with few small spines or tubercles (male), or with 2 or 3 strong spines (female). Palm 1.1–1.2 (male) or 1.0–1.1 (female) length of carpus; dorsal surface flat, with 1–3 tubercles (male) or spines (female) proximally in longitudinal row along midline or slightly mesiad of, and with additional longitudinal row of tubercles and/or blunt spines (male) or spines (female) in midline or slightly laterad of, not extending onto fixed finger; dorsomesial margin with row of tubercles and/or blunt spines (male) or spines (female); dorsolateral margin with row of tubercles and/or blunt spines (male) or spines (female) extending onto fixed finger for approximately half length; fixed finger terminating in corneous claw, cutting edge with variouslysized calcareous teeth proximally and row of tiny calcareous teeth distally (male, Fig. 15D View FIGURE 15 ), or with 1–4 comparatively large calcareous teeth proximally and row of small calcareous and sharp corneous teeth distally (female). Carpus 0.9–1.1 (male) or 0.7–0.8 (female) length of merus; mesial and lateral faces unarmed or with scattered tubercles; dorsomesial margin with row of 3–7 spines or tubercles (male), or with 2–4 strong spines (female); dorsolateral margin with row of tubercles or small spines (male), or with row of 36 strong spines (female). Merus with lateral and mesial faces unarmed or tuberculate ventrally; ventromesial margin unarmed or tuberculate, and/or with 1 spine (male), or with 2 or 3 strong spines (female). Ischium unarmed or with tubercles on ventromesial margin (male), or with row of protuberances on ventromesial margin and sharp spine on ventrolateral margin (female).
Left cheliped ( Fig. 17 View FIGURE 17 ) slender, armature of chela stronger in females ( Fig. 17E–G View FIGURE 17 ) than in males ( Fig. 17 View FIGURE 17 AD). Dactyl 0.8–0.9 length of palm, terminating in sharp corneous claw; dorsomesial margin unarmed or with 1–3 spines; cutting edge ( Fig. 17D View FIGURE 17 ) with row of small corneous teeth. Palm 0.6–0.7 length of carpus; dorsal surface with longitudinal row of 2–5 spines or tubercles; dorsomesial margin with row of 3 or 4 spines or tubercles; dorsolateral margin with row of spines extending onto fixed finger proximally; fixed finger terminating in sharp corneous claw, cutting edge ( Fig. 17D View FIGURE 17 ) with row of corneous teeth. Carpus 0.9–1.0 length of merus, basal portion of spines on surface often prominently swollen; dorsomesial margin with row of 4 or 5 strong spines, distalmost very large and sometimes terminally bifid; dorsolateral margin with row of 4 or 5 strong spines. Merus with ventromesial margin bearing 1 or 2 strong spines; ventrolateral margin unarmed or with 1 strong spine. Ischium with 1 or 2 spines on ventromesial margin.
Second ( Fig. 18A–D View FIGURE 18 ) and third ( Fig. 18E–F View FIGURE 18 ) pereopods generally similar; second shorter and carpal armature stronger than third. Dactyls 0.8–0.9 (second) or 1.0–1.1 (third) length of propodi, each terminating in strong corneous claw; slightly curved ventrally in lateral view; ventral margins each generally with 3 (up to 5) corneous spines. Propodi 1.7– 1.8 (second) or 1.9–2.0 (third) length of carpi; ventrodistal margins each with sharp corneous spine. Carpi 0.6–0.7 length of meri; dorsal surfaces each with 3–5 strong spines, basal portions of spines often swollen. Meri with 0–3 spines on ventral margins. In large individuals, lateral, mesial and dorsal surfaces of propodi, carpi and meri often with scattered low protuberances accompanied distally by few long setae.
Sternite of third pereopods with broad, subrectangular anterior lobe ( Fig. 14E View FIGURE 14 ) bearing setae anteriorly.
Fourth pereopod ( Fig. 14D View FIGURE 14 ) with dactyl bearing 0–3 corneous spines on lateral face ventrally; propodal rasp composed of several rows of scales.
Male with coxa of left fifth pereopod ( Fig. 14E View FIGURE 14 ) bearing welldeveloped sexual tube; no gonopore on right coxa.
Pleon with welldeveloped columellar muscle near anterior margin ventrally ( Fig. 14E View FIGURE 14 ).
Telson ( Fig. 14G–I View FIGURE 14 ) rounded or subtriangular, unarmed.
Coloration. Two color morphs were reported by Haig & Ball (1988) (as M. vexatus ). The specimens from Saparua and Seram were reported to have the shield mottled gray and cream, or green and white; ocular peduncles transparent, with black mottling, or mottled green and white; corneas salmon pink or off white; antennules transparent but for black stripe or row of black dots dorsally; antennal peduncles with green mottling; flagellum transparent; meri of chelipeds with brownish mottling on white background, carpi and chelae dirty white; second and third pereopods basically transparent, with mottled brown and cream, propodi and dactyls each with narrow brown longitudinal stripe on lateral face. Specimens from Banda were described with the ocular peduncles uniform olive drab; antennules white except for purple stripe dorsally; antennal peduncles mottled red and white; flagellum transparent; right cheliped purplish pink, left with proximal segments mottled olive drab and transparent, palm pink; dactyls and propodi of second and third pereopods each with narrow dark longitudinal stripe on lateral face, carpi with fine red mottling on white/transparent background, meri and ischia purplish pink.
I examined the color in two living specimens of this species from Japan. Although color patterns were sometimes irregular, they were somewhat different from those reported by Haig & Ball (1988). The specimen in Fig. 19A & B View FIGURE 19 has the shield mottled green and white, with a pair of salmon pink areas anteriorly; ocular peduncles with red mottling on salmon pink background; corneas dark salmon pink; antennules salmon pink, with black stripe dorsally; antennal peduncles salmon pink; flagellum transparent; chelipeds generally salmon pink; second and third pereopods basically salmon pink, dactyls each with narrow brown longitudinal stripe on lateral face. The specimen in Fig. 19C View FIGURE 19 has the shield mottled green and white, with pair of darker areas anteriorly; ocular peduncles with distal half green and proximal half salmon pink, with red mottling; corneas dark green; antennules generally transparent, with black stripe dorsally; antennal peduncles generally transparent; flagellum transparent; chelipeds with chelae generally salmon pink, meri and carpi greenish; second and third pereopods basically slightly greenish light brown, dactyls each with narrow brown longitudinal stripe on lateral face.
Despite differences in color patterns in life between individuals, preserved specimens exhibit similar color patterns, viz., numerous brown dots covering the antennular and antennal peduncles as well as the ocular peduncles ( Fig. 14B View FIGURE 14 ).
Remarks. The syntypes of Micropagurus polynesiensis consist of two right chelipeds, three ambulatory pereopods and bodies of two females and one male, in which all chelipeds and ambulatory pereopods are detached. The two chelipeds are morphologically very similar and slender, so they most probably belong to the two female specimens.
Nobili (1906, 1907) made no mention of the number of specimens he examined. Consequently, I could not determine if they were all that Nobili (1906, 1907) used for the description. Nevertheless, morphological features of one of the right chelipeds of the syntypes agree well with that illustrated by Nobili (1907).
Haig & Ball's (1988) description for Micropagurus vexatus was so detailed that I was able to identify specimens very easily. I initially identified the specimens before seeing the syntypes of M. polynesiensis , and, as a result, I recognized many " M. vexatus " specimens from the MNHN collection. Haig & Ball (1988) made no mention of the sexual dimorphism in this species, but I found that the morphology of the chelipeds was sexually dimorphic; the female cheliped was slenderer than the male. However, when I later examined the syntypes of M. polynesiensis , I found that the two chelipeds of the syntypes were quite similar to the female chelipeds of M. vexatus . Additionally, morphological features of the shield, ambulatory pereopods and telson of the syntypes M. polynesiensis agreed very well with those of M. vexatus . Consequently, I concluded that M. vexatus was a junior synonym of M. polynesiensis .
When Haig & Ball (1988) described M. vexatus , they did not examine the types of M. polynesiensis directly, but, instead, asked the late Mme M. de Saint Laurent to examine them. Haig & Ball (1988: 184) stated (in parentheses by AA) "Sketches of the shield, anterior appendages, and chelipeds of M. polynesiensis , provided by M. de Saint Laurent, show that it differs from our new species (= M. vexatus ) in the greater number of spines on the chela and carpus of the chelipeds, and in lacking a fringe of setae on the ocular acicles (= setae arising just proximal to the marginal spines)."
Nine lots of nontype specimens identified as M. polynesiensis are housed in the MNHN. However, my reexamination of these has shown that two lots (MNHNPg 3294, 7277) are M. spinimanus , n. sp., and three lots (MNHNPg 2766, 3404, 7278) are M. polynesiensis . The identities of the remaining four lots (MNHNPg 3295, 3296, 3297, 3298) could not be determined to species because of damage.
Regarding the differences between M. vexatus and M. polynesiensis pointed out by Haig & Ball (1988), viz., spination on the chelipeds, I could not detect any differences between Haig & Ball's (1988) description of the chelipeds of M. vexatus and the chelipeds of the syntypes of M. polynesiensis . However, among the nontype specimens of M. polynesiensis , there are specimens (MNHNPg 3294, 7277) with greater numbers of spines on the chelipeds than those of M. vexatus . But these specimens are now reassigned to M. spinimanus , n. sp. It is highly probable that M. Saint Laurent, believing that all the material was conspecific, actually sketched the chelipeds of a specimen of M. spinimanus . Regarding the second difference, viz., the absence of fringe of setae arising just proximal to the marginal spines on the ocular acicles in M. polynesiensis , my reexamination of the syntypes has revealed that the ocular acicles of all three specimens have a fringe of setae.
Spination of the right cheliped in males of this species is the weakest among Micropagurus species ; the midline of the dorsal face of the palm often is provided with only a row of small tubercles ( Fig. 15A View FIGURE 15 ). However, the same surfaces in males of other species are armed with single or multiple rows of sharp spines. If color patterns are preserved on the specimens, this species is easily separated from other species in having numerous brown dots on the antennular and the antennal peduncles as well as the ocular peduncles. None of other species have such color patterns. If the color pattern has faded, however, females of this species are sometimes difficult to separate from females of M. devaneyi .
Distribution. Western Pacific: Loyalty Islands, New Caledonia, Philippine Islands, Japan; 2– 44 m. Indian Ocean: Indonesia, Seychelles; 32– 55 m.
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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Genus |
Micropagurus polynesiensis ( Nobili, 1906 )
Asakura, Akira 2005 |
Micropagurus polynesiensis
Poupin, J. 1996: 18 |
Haig, J. & Ball, E. E. 1988: 184 |
Micropagurus vexatus
Haig, J. & Ball, E. E. 1988: 181 |
Anapagurus polynesiensis
Chevalier, J. P. & Denizot, M. & Mougin, J. L. & Plessis, Y. & Salvat, B. 1968: 119 |
Forest, J. 1956: 1056 |
Nobili, G. 1907: 372 |
Nobili, G. 1906: 260 |