Elamena minuta A. Milne-Edwards, 1873

Poore, Gary C. B., Guinot, Danièle, Komai, Tomoyuki & Naruse, Tohru, 2016, Reappraisal of species attributed to Halicarcinus White, 1846 (Crustacea: Decapoda: Brachyura: Hymenosomatidae) with diagnosis of four new genera and one new species from New Ireland, Papua New Guinea, Zootaxa 4093 (4), pp. 480-514 : 493-494

publication ID

https://doi.org/ 10.11646/zootaxa.4093.4.2

publication LSID

lsid:zoobank.org:pub:5E0BF4DB-04EA-4A9A-BF47-901DF84FFD39

DOI

https://doi.org/10.5281/zenodo.5668406

persistent identifier

https://treatment.plazi.org/id/753D87B8-050B-FD4A-FF22-FD52FE04FEC1

treatment provided by

Plazi

scientific name

Elamena minuta A. Milne-Edwards, 1873
status

 

Micas Ng & Richer de Forges, 1996

Micas Ng & Richer de Forges, 1996: 265.

Type species. Elamena minuta A. Milne-Edwards, 1873 , by original designation.

Diagnosis. Rostrum a broadly triangular projection, or a simple rod ( M. lucasi only); apex without long setae. Supraocular eave obsolete, without preocular definition or defined anteriorly by pseudorostral element of a broad triangular lobe; without postocular structures. Carapace as long as wide; with well-developed grooves, including complete or partial median cardiac groove; hymenosomian groove completely surrounding dorsum but only weakly isolating rostrum. Thoracic sternum of male with pleonal cavity defined laterally and anteriorly by sharp rim, about 0.8 of sternal length; locking button on sternite 6 unknown. Male pleomeres 1 and 2 free, 3–4 fused, 5 and pleotelson free, or pleomeres 3–pleotelson fused; pleomere 1 as wide as pleomere 2; pleonal margin tapering most strongly from pleomere 3–4. Thoracic sternum of female with paired vulvae anteriorly on membranous medial area; with paired branchiosternal canal apertures ventrally on sternite 8. Pleon of ovigerous female discoid, pleomeres 2–5 free or fused. Eyestalks compact, without tubercle on anterior margin. Maxilliped 3 endopod and exposed exopod covering almost all or three-quarters of lateral width of buccal cavern when closed; axial length of ischium-merus twice maximum ischium width; merus without expanded anterolateral lobe. Cheliped in male with grossly swollen barrel-like propodus, fingers with finely denticulate cutting edges, gape without felt of setae; dactylus usually with simple proximal tooth. Ambulatory legs elongate (pereopod 2 3 times as long as carapace length); with articulation between propodus and dactylus supported by short narrow plate on each side; dactyli curved, with 1 or 2 subterminal teeth. Gonopod 1 with swollen base, narrow distal section tapering through a sharp proximal ventral curvature and twist, with apex acute sharply bent ventrally. Female pleopods 2–5 biramous.

Included species. Micas afecundus (Lucas, 1980) (ex Halicarcinus ); M. falcipes Ng & Richer de Forges, 1996; M. filholi (De Man, 1888) (ex Elamena ) n. comb.; M. lucasi (Richer de Forges, 1993) (ex Halicarcinus ); M. minutus (A. Milne-Edwards, 1873) (ex Elamena ).

Distribution. Tropical western Pacific, subtidal to 244 m.

Remarks. Micas differs from all other taxa discussed here in having a twisted gonopod 1 with the apex bent and in having two subapical teeth on the dactylus of ambulatory legs rather than a row of several along its length. Grouping these five species on the basis of gonopod 1 (known in only three of the five species) and similar pereopodal dactyli is far from satisfactory. Micas lucasi with its rod-like rostrum is the odd one out but is too poorly known to place elsewhere with confidence. The proepistome, epistome and gonopod 2 have not been illustrated for any species in this genus.

Aletheiana Ng & Lukhaup, 2015, is known from a single cave-dwelling Indonesian species, A. tenella Ng & Lukhaup, 2015 . This too has simple dentition on the ambulatory dactyli, one subterminal tooth plus 0–3 smaller more proximal teeth. The genus differs from Micas in having narrow maxillipeds 3 only partially covering the buccual cavern (Ng & Lukhaup 2015: fig. 3E) whereas maxilliped 3 is broad and covering at least three-quarters of the buccal cavern in species of Micas (Ng & Chuang 1996: fig: 19; Ng & Richer de Forges 1996: fig. 4G). Aletheiana tenella has a more reduced rostrum and a simpler gonopod 1 without a strong curve and twist.

Another monotypic genus, Apechocinus Ng & Chuang, 1996 , shares with Micas broad maxillipeds 3, elongate and slender ambulatory legs, and a strongly twisted distal section of gonopod 1 (Ng & Chuang, 1996: fig. 4). The genus differs from Micas in having much broader rostrum that merges with the pseudorostral element (Ng & Chuang, 1996: fig. 4A) whereas the rostrum is narrower and the pseudorostral element, if any, is clearly separated from the rostrum in species of Micas ( Fig. 4 View FIGURE 4 b; Lucas 1980: fig. 3G; Richer de Forges 1993: fig. 2; Ng & Richer de Forges 1996: figs. 3A, 4B).

Kingdom

Animalia

Phylum

Arthropoda

Class

Malacostraca

Order

Decapoda

InfraOrder

Brachyura

Family

Hymenosomatidae

Genus

Elamena

Kingdom

Animalia

Phylum

Arthropoda

Class

Malacostraca

Order

Decapoda

InfraOrder

Brachyura

Family

Hymenosomatidae

Genus

Micas

Kingdom

Animalia

Phylum

Arthropoda

Class

Malacostraca

Order

Decapoda

InfraOrder

Brachyura

Family

Hymenosomatidae

Genus

Micas

Kingdom

Animalia

Phylum

Arthropoda

Class

Malacostraca

Order

Decapoda

InfraOrder

Brachyura

Family

Hymenosomatidae

Genus

Rhynchoplax

Kingdom

Animalia

Phylum

Arthropoda

Class

Malacostraca

Order

Decapoda

InfraOrder

Brachyura

Family

Inachidae

Genus

Achaeus

Kingdom

Animalia

Phylum

Arthropoda

Class

Malacostraca

Order

Decapoda

InfraOrder

Brachyura

Family

Hymenosomatidae

Genus

Rhynchoplax

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