Plagusiidae, Dana, 1851
publication ID |
https://doi.org/10.11646/zootaxa.3665.1.1 |
publication LSID |
lsid:zoobank.org:pub:8358B363-BEE3-416D-96CA-8614E38B61D5 |
persistent identifier |
https://treatment.plazi.org/id/03BB9C75-FF6F-FF1A-FF78-FE62FCBFFCBC |
treatment provided by |
Felipe (2021-08-25 03:06:50, last updated by Plazi 2023-11-04 18:44:43) |
scientific name |
Plagusiidae |
status |
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Families Plagusiidae View in CoL and Percnidae
The male gonopore is sternal. It opens very close, seemingly joined, to the P5 coxa, as in Plagusia depressa ( Fig. 23B View FIGURE 23 ; see H. Milne Edwards 1836–1844, Atlas , pl. 23, fig. 3d; Guinot 1979a: 209, fig. 52E), P. squamosa (see N.K. Ng, Davie, Schubart & Ng 2007: fig. 4C), Guinusia dentipes (see Karasawa & Kato 2001: fig. 2.17, as P. dentipes ), Davusia glabra (see Guinot 1979a: pl. 18, fig. 9, as Plagusia glabra ; 2007: 29). The sternal gonopore also opens close to P5 coxa in Percnon planissimum (see Guinot 1979a: pl. 23, fig. 2; Rodríguez 1992: fig. 11E; Karasawa & Kato 2001: fig. 2.18). This proximity of the gonopore to the P5 coxa led Brocchi (1875: 81, as Acanthopus planissimus ) to assume that the gonopore was coxal, with the ejaculatory duct connected to the appendage and not to the sternum. Our dissections demonstrate, nonetheless, a direct connection between the gonad and the sternal gonopore ( Fig. 33 View FIGURE 33 ) so the condition is truly sternal in both families. The gonopore is large and opens far from and markedly below suture 7/8, on the sternal region just above the P5 coxo-sternal condyle, which is surrounded by a conspicuously elongated episternite 7.
The configuration is rather similar in Plagusia , Percnon , Davusia and Guinusia , and varies only in the details. In the species of these genera that were examined the outer portion of sternite 8 remains laterally exposed and shows as a distinct plate, similar to the preceding sternites. Sternite 8 was erroneously described as being completely concealed by the abdomen although a small anterior portion is laterally visible ( Guinot 1979a: 209, pl. 18, fig. 9, as Plagusia glabra ). In Plagusia , Percnon , Davusia , and Guinusia , episternite 7 is posteriorly elongated so that it is close to or even reaches the narrow expansion of sternite 8 in the proximity of the P5 coxo-sternal condyle. Episternite 7 and the portion of sternite 8 bearing the gynglyme for the P5 coxa are joined in Plagusia , Davusia , and Guinusia , but are more distant in Percnon . This posterior area of sternite 8 remains partially exposed dorsally, a small portion being slightly dorsally visible (e.g., in Plagusia depressa and P. squamosa ); but it may be smaller, hardly visible (e.g., in P. immaculata , Guinusia chabrus ), and not visible at all in Davusia glabra . In Percnon , the posterior portion of sternite 8 laterally forms a raised, rounded plate, only partially concealed by the abdomen, a small exposed portion remaining visible on each side at the limit of abdominal somites 2 and 3, abdominal somites 3–5 being fused.
In Plagusia View in CoL and Guinusia View in CoL , the penis consists of a large, oval, sclerotised proximal portion, and a thick papilla; in Daviusa, the proximal portion is smaller, elongated, the papilla is short, pointed. In Percnon View in CoL , the sclerotised proximal portion is much reduced and the papilla is foliaceous. The tribe Davusiini Števčić, 2011 View in CoL , established within Plagusiidae View in CoL Plagusiinae , by being simply based only on the diagnosis of Davusia View in CoL (as type genus), without consideration of the other genera, is an oversimplification, the Plagusiinae not being diagnosed and differentiated. It is possible that Plagusiidae View in CoL consists of several groups of genera, but a rigorous taxonomic revision of the family, such as that of Schubart & Cuesta (2010), must first be undertaken.
Euchirograpsus H. Milne Edwards, 1853 View in CoL , shows an elongated episternite 7 (as in many grapsoid genera), which reaches the narrow expansion of sternite 8 receiving the P5 coxo-sternal condyle. There is a complete junction along episternite 7 and sternite 8; the male gonopore is far from suture 7/8 and partially encircled by sternite 8. When the abdomen is closed, a small portion of sternite 8 may be anteriorly exposed and laterally visible on each side at the limit of abdominal somites 2 and 3, as a narrow ( E. liguricus View in CoL ) or hardly discernible ( E. americanus View in CoL ) portion, or not at all visible ( E. timorensis View in CoL ). The male gonopore is large. The penis is well developed, with a long, weakly sclerotised or unsclerotised proximal portion, and an elongated papilla (N.K. Ng & Martin 2010: 232, 239, 244, figs. 5, 7). In Miersiograpsus Türkay, 1978 ( Türkay 1978) View in CoL , also included in the Plagusiidae View in CoL ( Davie 2002: 438; Poore 2004: 514; Ng, Guinot & Davie 2008: 218; Schubart & Cuesta 2010), the disposition is similar to that of Euchirograpsus View in CoL , sternite 8 being exposed dorsally with a small portion visible on each side at the limit of abdominal somites 2 and 3. Zoeae of E. americanus View in CoL show close relationships with those of Plagusiidae ( Wilson 1980) View in CoL .
Percnon View in CoL has been recently placed in its own family, Percnidae Števčić, 2005 View in CoL , whereas Plagusia View in CoL , Davusia View in CoL , and Guinusia View in CoL , together with Euchirograpsus View in CoL and Miersiograpsus View in CoL , were grouped in the Plagusiidae ( Schubart & Cuesta 2010) View in CoL , instead of the subfamilial ranks recognised by Ng, Guinot & Davie (2008: 218). Molecular analyses using 16S rDNA sequence data of Euchirograpsus americanus View in CoL , Percnon gibbesi View in CoL and Plagusia squamosa View in CoL by Wetzer et al. (2009: 486, 487, fig. 1) similarly did not support the monophyly of the family Plagusiidae View in CoL , Percnon View in CoL not being allied to the other two genera. As a confirmation of their first results (Schubart, Diesel, Neigel & Felder 2000a; Schubart et al. 2006), recent studies combining molecular and larval data by Schubart & Cuesta (2010) concluded to the separation of the Percnidae View in CoL .
A large and prominent press-button for the abdominal-locking mechanism is characteristic of Plagusia View in CoL and Percnon View in CoL , with only a few variations. Its corneous aspect is due to a scaly paving on the upper portion, and this microstructure seems to be typical ( Guinot 1979a: 144, pl. 18, figs. 9–11, pl. 23, figs. 2, 3; Guinot & Bouchard 1998: 680, fig. 26F; Bouchard 2000: 189, fig. 46A–D). Associated to this strong sternal prominence, a deep, rimmed socket persists and functions throughout life in plagusiid females ( Guinot & Bouchard 1998: 680, fig. 26C), only a sternal scar remaining visible in post-puberty females. Such a persistence of the button in large females does not occur in the Percnidae View in CoL . The microstructure of the locking system, which improves contact between the involved surfaces and increases the efficiency of the locking mechanism, is probably a conservative feature and seems to constitute a reliable taxonomic character, although its needs to be compared in both the Plagusiidae View in CoL and Percnidae View in CoL . The study of the microstructure of the press-button needs to be extended to a larger sample of species of these two groups to determine at which taxonomic rank this particular structure adequately applies. The press-button of Euchirograpsus View in CoL , however, is particularly acute, corresponding to a socket posteriorly defined by a strongly calcified border.
Adult morphology had traditionally placed the species of Plagusia ( Dawson 1987) and those of the highly derived Percnon in a single family ( Crosnier 1965; Davie 2002). Schubart & Cuesta (2010) recognised homoplasy relation (convergence) between the two distinct families, Plagusiidae and Percnidae , which share, however, incipient or deep antennular cleft in the frontal margin ( Crosnier 1965: figs. 130, 131, pl. 7; Poupin 1994b: fig. 60) and a similar microstructure of the press-button. Molecular data show no affinity of Plagusiidae with the Gecarcinidae ( Schubart & Cuesta 2010: 293, figs. 1, 2).
Bouchard, J. - M. (2000) Morphologie fonctionelle des systemes de retention de l'abdomen chez les Brachyoures (Crustacea Decapoda). Microstructures; implications phylogenetiques et systematiques. Unpublished doctoral thesis, Museum national d'Histoire naturelle, Paris, 694 pp.
Brocchi, P. (1875) Recherches sur les organes genitaux males des Crustaces Decapodes. Annales de Sciences naturelles (Zoologie), (6) 2, 1 - 131.
Crosnier, A. (1965) Crustaces Decapodes Grapsidae et Ocypodidae. In: Faune de Madagascar, 18. ORSTOM, CNRS, Paris, 153 pp.
Davie, P. J. F. (2002) Crustacea: Malacostraca: Eucarida (Part 2): Decapoda-Anomura, Brachyura. In: Wells, A. & Houston, W. W. K. (Eds.) Zological Catalogue of Australia, vol. 19.3 B. CSIRO Publishing Australia, Melbourne, xiv + 641 pp.
Dawson, E. W. (1987) A key to the world species of Plagusia (Crustacea: Brachyura), with a new record of P. depressa tuberculata Lamarck from New Zealand. National Museum of New Zealand Records, 3 (4), 37 - 45.
Guinot, D. (1979 a) Donnees nouvelles sur la morphologie, la phylogenese et la taxonomie des Crustaces Decapodes Brachyoures. Memoires du Museum national d'Histoire naturelle, ser. A, Zoologie, 112, 1 - 354.
Guinot, D. & Bouchard, J. - M. (1998) Evolution of the abdominal holding systems of brachyuran crabs (Crustacea, Decapoda, Brachyura). Zoosystema, 20 (4), 613 - 694.
Karasawa, H. & Kato, H. (2001) The systematic status of the genus Miosesarma Karasawa, 1989 with a phylogenetic analysis within the family Grapsidae and a review of fossil recors (Crustacea: Decapoda: Brachyura). Paleontological Research, 5 (4), 259 - 275.
Milne Edwards, H. (1853) Memoire sur la famille des Ocypodiens. Annales des Sciences naturelles (Zoologie), ser. 3, 20, 163 - 228, pls. 6 - 11.
Ng, N. K., Davie, P. J. F., Schubart, C. D. & Ng, P. K. L. (2007) Xenograpsidae, a new family of grapsoid crabs (Crustacea: Brachyura) associated with shallow water hydrothermal vents. Raffles Bulletin of Zoology, suppl. 16, 233 - 256.
Ng, P. K. L., Guinot, D. & Davie, P. J. F. (2008) Systema Brachyurorum: Part 1. An annotated checklist of extant brachyuran crabs of the world. Raffles Bulletin of Zoology, suppl. 17, 1 - 286. [updates at http: // rmbr. nus. edu. sg / research / cotw / supplement 17. php]
Ng, N. K. & Martin, J. W. (2010) Two new species of grapsoid crabs of the genus Euchirograpsus (Decapoda, Brachyura, Grapsoidea, Plagusiidae) from the Philippines and the Hawaiian Islands. In: Castro, P., Davie, P. J. F., Ng, P. K. L. & Richer de Forges, B. (Eds.), Studies on Brachyura: A Homage to Daniele Guinot. Crustaceana Monographs, 11, 229 - 249.
Poore, G. C. B. (2004) Marine Decapod Crustacea of Southern Australia. A Guide to Identification. CSIRO Publishing, Collingwood, Melbourne, 517 pp.
Rodriguez, G. (1992) The freshwater crabs of America. Family Trichodactylidae and Supplement to the Family Pseudothelphusidae. Faune Tropicale, ORST 0 M, Paris, 31, 1 - 189. http: // dx. doi. org / 10.1163 / 193724094 x 00588
Schubart, C. D., Cannicci, C., Vannini, M. & Fratini, S. (2006) Molecular phylogeny of grapsoid crabs (Decapoda, Brachyura) and allies based on two mitichondrial genes for a proposal for refraining from current superfamily classification. Journal of Zoological Systematics and Evolutionary Research, 44 (3), 193 - 199. http: // dx. doi. org / 10.1111 / j. 1439 - 0469.2006.00354. x
Schubart, C. D. & Cuesta, J. A. (2010) Phylogenetic relationships of the Plagusiidae Dana, 1851 (Brachyura), with description of a new genus and recognition of Percnidae Stevcic, 2005, as an independent family. In: Castro, P., Davie, P. J. F., Ng, P. K. L. & Richer de Forges, B. (Eds.), Studies on Brachyura: A Homage to Daniele Guinot. Crustaceana Monographs, 11, 279 - 299.
Stevcic, Z. (2005) The reclassification of brachyuran crabs (Crustacea: Decapoda: Brachyura). Natura Croatica (Fauna Croatica), 14, suppl. 1, 1 - 159.
Stevcic, Z. (2011) Addition to the reclassification of brachyuran crabs (Crustacea: Decapoda: Brachyura). Part I. New taxa. Natura Croatica (Fauna Croatica), 20 (1), 125 - 139.
Turkay, M. (1978) Zwei neue Grapsiden - Arten aus dem Indopazifik (Euchirograpsus madagascariensis n. sp. und Miersiograpsus australiensis n. sp.) mit Einfuhrung von Miersiograpsus n. gen. (Crustacea: Decapoda: Grapsidae). Senckenbergiana biologica, 59, 133 - 141.
Wetzer, R., Martin, J. W. & Boyce, S. L. (2009) Evolutionary origin of the gall crabs (family Cryptochiridae) based on 16 S rDNA sequence data. In: Martin, J. W., Crandall, K. A. & Felder, D. L. (Eds.), Decapod Crustacean Phylogenetics. Crustacean Issues, 18, 475 - 490.
Wilson, K. A. (1980) Studies on decapod crustaceans from the Indian River region of Florida. V. The larval development under laboratory conditions of Euchirograpsus americanus A. Milne Edwards, 1888 (Crustacea Decapoda: Grapsidae) with notes on grapsid subfamilial larval characters. Bulletin of Marine Science, 30 (4), 756 - 775.
FIGURE 23. Sternal male gonopores in Thoracotremata. A, Cardisoma carnifex (Herbst, 1796) (Gecarcinidae), male, Madagascar (MNHN-B29589); B, Plagusia depressa (Fabricius, 1775) (Plagusiidae), male 40.0 × 44.0 mm, Senegal (MNHN- B11693): schematic view (see Fig. 33A) (abdomen indicated by dotted line); C, Ucides cordatus (Linnaeus, 1763) (Ucididae), male 70.0 × 93.0 mm, Brazil (MNHN-B13237) (abdomen indicated by dotted line); D, Grapsus grapsus (Linnaeus, 1758) (Grapsidae), male 57.0 × 60.0 mm, Clipperton I. (MNHN-B11538): schematic representation after dissection; E, F, Ocypode cursor (Linnaeus, 1758) (Ocypodidae), male 38.0 × 49.0 m, Senegal (MNHN): E, before dissection along dotted line; F, after dissection showing ejaculatory duct perforating somite 8, instead of P5 coxa. c, P5 coxo-sternal condyle; cx5, P5 coxa; e.d., ejaculatory duct; e7, episternite 7; g, gonopore; p, penis; p5, pereopod 5; 7, 8, sternites 7, 8; 7/8, thoracic sternal suture 7/8.
FIGURE 33. Thoracotreme disposition. A, Plagusia squamosa (Herbst, 1790) (Plagusiidae), male cw 55.0 mm (dissected), French Polynesia (MNHN-B8889): trajectory of vas deferens directly connecting gonad to sternal gonopore. B, Ostracotheres tridacnae (Rüppell, 1830) (Pinnotheroidea), male, 9.0 × 8.6 mm, Egypt, Suez (MNHN-B10578): thoracic sternum; C, Pinnotheres pisum (Linnaeus, 1767) (Pinnotheroidea), male 4.7 × 4.6 mm, Bay of Biscay, La Rochelle (MNHN-B10604): male gonopore (B, C, after Guinot 1979a: figs. 24D, 53G respectively). cx5, P5 coxa; g, sternal gonopore; j, lateral extension of sternite 4 resulting in incomplete thoracic sternum/pterygostome junction; m.l., median line; mxp3, external maxillipeds; p, penis; t, telson; v.d., vas deferens; 3–8, thoracic sternites 3–8; 4/5–7/8, thoracic sternal sutures 4/5–7/8. Scale bar: 1 mm (A).
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Kingdom |
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Phylum |
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Class |
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Order |
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Family |
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Genus |
Plagusiidae
GUINOT, DANIÈLE, TAVARES, MARCOS & CASTRO, PETER 2013 |
Davusiini Števčić, 2011
Stevcic 2011 |
Guinusia
Schubart & Cuesta 2010 |
Guinusia
Schubart & Cuesta 2010 |
Davusia
Guinot 2007 |
Davusia
Guinot 2007 |
Percnidae Števčić, 2005
Stevcic 2005 |
Percnidae
Stevcic 2005 |
Percnidae
Stevcic 2005 |
Percnidae
Stevcic 2005 |
Miersiograpsus Türkay, 1978 ( Türkay 1978 )
Turkay 1978 |
Miersiograpsus
Turkay 1978 |
E. timorensis
Turkay 1975 |
E. americanus
A. Milne-Edwards 1880 |
E. americanus
A. Milne-Edwards 1880 |
Euchirograpsus americanus
A. Milne-Edwards 1880 |
Euchirograpsus
H. Milne Edwards 1853 |
E. liguricus
H. Milne Edwards 1853 |
Euchirograpsus
H. Milne Edwards 1853 |
Euchirograpsus
H. Milne Edwards 1853 |
Euchirograpsus
H. Milne Edwards 1853 |
Plagusiidae
Dana 1851 |
Plagusiinae
Dana 1851 |
Plagusiinae
Dana 1851 |
Plagusiidae
Dana 1851 |
Plagusiidae
Dana 1851 |
Percnon
Gistel 1848 |
Percnon
Gistel 1848 |
Percnon
Gistel 1848 |
Percnon
Gistel 1848 |
Plagusia
Latreille 1804 |
Plagusia
Latreille 1804 |
Plagusia
Latreille 1804 |