412 research outputs found
Thalamita gloriensis Crosnier 1962
No full text<i>Thalamita gloriensis</i> Crosnier, 1962 <p> <i>Thalamita gloriensis</i> Crosnier, 1962: 98, figs. 155, 156 bis <i>d</i>, 159, 160, 165–167, 169 [type locality: <i>îles Glorieuses</i> (western Indian Ocean); holotype: MNHN-B6204].</p> <p> <b>Hawaiian Is. record:</b></p> <p> <i>Thalamita gloriensis</i> Crosnier, 1962 — Stephenson & Rees 1967: 76 [O‘ahu].</p> <p> <b>Taxonomy.</b> Crosnier (1962), Stephenson & Rees (1967), Vannini & Innocenti (2000)</p> <p> <b>Geographical distribution.</b> Across Indo-West Pacific region.</p> <p> <b>Habitat</b>. Intertidal, shallow subtidal.</p>Published as part of <i>Castro, Peter, 2011, Catalog of the anomuran and brachyuran crabs (Crustacea: Decapoda: Anomura, Brachyura) of the Hawaiian Islands 2947, pp. 1-154 in Zootaxa 2947 (1)</i> on page 74, DOI: 10.11646/zootaxa.2947.1.1, <a href="http://zenodo.org/record/5283044">http://zenodo.org/record/5283044</a>
Thalamita stephensoni Crosnier 1962
No full text<i>Thalamita stephensoni</i> Crosnier, 1962 <p> <i>Thalamita stephensoni</i> Crosnier, 1962: 140, figs. 241–248 [type locality: Madagascar; holotype: MNHN-B6295]. <b>Hawaiian Is. record:</b></p> <p> <i>Thalamita stephensoni</i> Crosnier, 1962 — Stephenson 1972: 152 [O‘ahu].</p> <p> <b>Taxonomy.</b> Crosnier (1962), Vannini & Innocenti (2000)</p> <p> <b>Geographical distribution.</b> Across Indo-West Pacific region.</p> <p> <b>Habitat</b>. Intertidal</p>Published as part of <i>Castro, Peter, 2011, Catalog of the anomuran and brachyuran crabs (Crustacea: Decapoda: Anomura, Brachyura) of the Hawaiian Islands 2947, pp. 1-154 in Zootaxa 2947 (1)</i> on page 77, DOI: 10.11646/zootaxa.2947.1.1, <a href="http://zenodo.org/record/5283044">http://zenodo.org/record/5283044</a>
Hymenopenaeus fallax Crosnier & Dall, 2004, sp. nov.
No full text<i>Hymenopenaeus fallax</i> sp. nov. (Figs. 6 ñ8) <p> <i>Haliporus equalis</i> Rathbun, 1906: 905 [non Bate, 1888].</p> <p> <i>Hymenopenaeus</i> cf. <i>obliquirostris</i>. — Crosnier, 1989: 47, figs. 2c, 4b (under <i>H. equalis</i>).</p> <p> <b>Types. Hawaii:</b> <i>Albatross</i> Exped., Stn 4106, Kaiwi Channel, 613–640 m, 24.07.1902, 1 ɗ <i>paratype</i> 16.3 mm and Ψ <i>holotype</i>, 28.7 mm (USNM 30919); Stn 4029, vic. Kauai Id, 875– 832 m, 24.06.1902, 1 ɗ <i>allotype</i> 18.8 mm (USNM 30918); Stn 3989, vic. Kauai Id, 914– 704 m, 11.06.1902, 1 Ψ <i>paratype</i> 21.8 mm (USNM 30914); Stn 4110, Kaiwi Channel, 821–841 m, 24.07.1902, 1 ɗ <i>paratype</i>, 18.2 mm (USNM 30922); Stn 4153, vic. Modu Manu Id, 1760–1937 m, 5.08.1902, 1 Ψ <i>paratype</i> 24.1 mm (USNM 30924).</p> <p> <b>Other material examined. Hawaii:</b> <i>Albatross</i> Exped., Kaiwi Channel, 627 m, 4.12.1891, 2 juv. 10.8 and 11.0 mm (USNM 30909); Stn 3471, Kaiwi Channel, 617 m, 4.12.1891, 2 juv. 10.5 mm (USNM 30910); Stn 3474, Kaiwi Channel, 686 m, 6.12.1891, 1 ɗ 16.1 mm; 1 Ψ (USNM 30911) from fish stomach; Stn 3475, Kaiwi Channel, 642 m, 6.12.1891, 1 Ψ 21.0 mm (USNM 30912); Stn 3988, Kauai Id, 857– 302 m, 11.06.1902, 1 juv. 11.1 mm (USNM 30913); Stn 4022, vic. Kauai Id, 729– 684 m, 21.06.1902, 2 Ψ 16.9 and 17.4 mm (USNM 30916); Stn 4028, vic. Kauai Id, 812–875 m, 24.06.1902, 1 Ψ 20.4 mm (USNM 30917); Stn 4107, Kaiwi Channel, 640–649 m, 24.07.1902, 2 ɗ 14.0 mm and 19.0 mm (USNM 30920); Stn 4108, Kaiwi Channel, 752–809 m, 24.07.1902, 1 Ψ 12.2 mm (USNM 30921); Stn 4112, Kaiwi Channel, 818– 791 m, 24.07.1902, 1 Ψ 14.5 mm (USNM 30923); Stn 4157, vic. Modu Manu Id, 1394–1829 m, 6.08.1902, 1 juv. 12.0 mm (USNM 30925); Stn 4166, vic. Modu Manu Id, 536–1463 m, 8.08.1902, 1 juv. 10.0 mm (USNM 30926).</p> <p> <b>Diagnosis.</b> Body cuticle smooth, without setae. Rostrum bearing 5 or 6 dorsal rostral teeth, none ventral. A postrostral carina, clearly defined, extending for three­quarters the distance between the cervical sulcus and the posterior border of the carapace. Hepatic, antennal, postantennal and branchiostegal spines slender, the last the strongest, with its tip varying from almost reaching to slightly exceeding the anterior edge of the carapace. Eye relatively small, colour a clear brown. Merus of the first pereopods without a fixed spine on the internal edge. Thelycum on sternite XIII, between the fourth pereopods, projecting in the form of the tip of a tongue, very flattened antero­posteriorly; the posterior part of the sternite bears on each side, two well­developed projecting transverse plates. Sternite XIV bears a prominent swelling, more or less in the shape of an escutcheon, and with a median ridge, which does not have a terminal tooth abutting the posterior of sternite XIII. Petasma with a median lobe whose extremity is divided into two elongate lobules, each terminating in a point, separated by a V­shaped opening; anterior lobule very asymmetric, with exterior edge very curved and interior edge almost straight; posterior lobule more symmetrical with the edges slightly curved; below these lobules on the external side, an inferior lobule regularly rounded and scarcely wider than long; lateral lobe showing on the external face an extended distal lobule, roughly ovoid, which partly covers the inferior lobule of the median lobe.</p> <p> <b>Coloration.</b> Unknown.</p> <p> <b>Size.</b> The largest female examined had a carapace of 28.7 mm, which corresponds with a total length of about 104 mm.</p> <p> <b>Etymology.</b> From the Latin <i>fallax</i>, deceptive, evoking the ease with which this species may be confused with <i>H. obliquirostris</i>.</p> <p> <b>Remarks.</b> This species is close to <i>H. obliquirostris,</i> having a well defined postrostral carina and the merus of the first pereopods lacking a fixed spine, contrary to that seen in other Indo­West Pacific <i>Hymenopenaeus</i> species. The rostrum and spines on the carapace, particularly the branchiostegal spine, closely resemble those of <i>H. obliquirostris</i>.</p> <p> <i>Hymenopenaeus fallax</i> may be easily separated from <i>H. obliquirostris</i> by comparison of features of the genitalia, particularly the thelycum. Thus the female <i>H. obliquirostris</i> has a strong trihedral dentiform projection on sternite XIII between the fourth pereopods, the edges sharper in juveniles (Fig. 4), whereas <i>H. fallax</i> has a tongue­like projection, flattened antero­posteriorly, directed obliquely towards the rear and more or less rounded (Fig. 7). In <i>H. obliquirostris</i> on sternite XIV, between the fifth pereopods, the escutcheonshaped swelling has a longitudinal median ridge with a strong anterior tooth which abuts the posterior edge of sternite XIII (Fig. 4 a), whereas in <i>H. fallax</i> the median ridge is strongly convex and stops well short of sternite XIII (Figs. 7 a, b, c). The posterior edge of sternite XIII with a median depression between two projections is much more developed in <i>H. fallax</i> (Fig. 7 d) than in <i>H. obliquirostris</i> (Fig. 4 c).</p> <p> In the males the distinction is more difficult to make on account of the variability observed. In general the petasma of <i>H. fallax</i> may be distinguished from that of <i>H. obliquirostris</i> by the external edge of the anterior distal lobule of the median lobe being more convex and the inferior lobule situated under the distal lobules much smaller and more rounded. Also, the distal ovoid lobule of the lateral lobe is relatively smaller than in <i>H. obliquirostris.</i> The differences described above are difficult to appreciate without having specimens of both species for comparison. An example of the variation encountered is given in figures 8d and e.</p> <p> <b>Distribution.</b> This species is not known outside the Hawaiian Islands. It was collected at a depth of 617 m and also between 1760–1937 m.</p>Published as part of <i>Crosnier, Alain & Dall, William, 2004, Redescription of Hymenopenaeus obliquirostris (Crustacea, Decapoda, Penaeoidea, Solenoceridae) and descriptions of two new species of Hymenopenaeus from the IndoWest Pacific, pp. 1-26 in Zootaxa 600</i> on pages 10-14, DOI: <a href="http://zenodo.org/record/158540">10.5281/zenodo.158540</a>
Grapsus fourmanoiri Crosnier 1965
No full textGrapsus fourmanoiri Crosnier, 1965 (Fig. 3E) Grapsus fourmanoiri Crosnier, 1965: 12-17, figs 4-6, pl. 3, fig. 1, table p. 16. CURRENT TAXONOMIC STATUS. — Grapsus fourmanoiri Crosnier, 1965. LECTOTYPE (by present designation). — MNHN-IU-2008-10635 (= MNHN-B11803), ♂ 28.0 × 31.7 mm, Nosy Bé, Madagascar, coll. and det. A. Crosnier. PRESERVATION OF THE LECTOTYPE. — In alcohol. RP1 missing. PARALECTOTYPES. — MNHN-IU-2014-11212 (= MNHN-B11531), 3♂ 22.6 × 25.2 – 24.2 × 27.8 mm, 1 ♀ 21.2 × 24.4 mm, 2 ovig. ♀ 24.1 × 28.6 – 29.5 × 33.4 mm, same data as lectotype. PRESERVATION OF THE PARALECTOTYPES. — In alcohol. REMARKS Crosnier (1965: 14, table p. 16) has based the species on several specimens from Nosy Bé, Madagascar, but he did not expressly mention any type specimens in his publication. He mentions in the text a large specimen (length: 34.1; width: 37.7 mm) and provides measurements of five males and two females in a table (Crosnier 1965: 16). Two lots of specimens deposited at the Muséum, MNHN-IU-2008-10635 (= MNHN-B11803) and MNHN-IU-2014-11212 (= MNHN-B11531) are labelled “ Syntypes ”. Our measurements of most of the specimens do not correspond to the dimensions provided by Crosnier (1965: 16), except for one male MNHN-IU-2008-10635 (= MNHN-B11803), 28.0 × 31.7 mm. This discrepancy can be easily accounted for by how the specimens were measured. The largest specimen (length: 34.1; width: 37.7 mm) could not be located. The next largest male specimen MNHN-IU-2008-10635 (= MNHN-B11803) is here designated as lectotype of G. fourmanoiri. The other specimens from the type series become paralectotypes. It is very likely that Crosnier (1965) has collected and examined more than eight specimens belonging to his type series. Actually, one specimen was donated to Leiden Museum by Crosnier in 1966 (RMNH D 22683, male 23.7 × 27.0 mm, Nosy Bé, Madagascar, coll. and det. A. Crosnier): it is indicated as syntype in the Catalogue of the Types of the Nationaal Natuurhistorisch Museum, Leiden, by Fransen et al. (1997: 123) and shows the same ‘type and form’ of label as the labels of the MNHN jars. This RMNH sample also becomes paralectotype. Fransen et al. (1997: 123, footnote) regarded two additional samples as syntypes of G. fourmanoiri, but this mention corresponds to an erroneous statement. Crosnier (1965: 17, footnote) wrote: “At Leiden, we have reexamined specimens from Banerjee (1960: 149) from Durban and Reunion Rocks, initially identified as Grapsus albolineatus ”. According to Fransen (pers. comm., December 2012), two samples (RMNH D3210, one female 32.5 × 35.0 mm, South Africa, Reunion Rocks, 28.X.1938, leg. L. D. Brongersma; RMNH D3250, 2 males 10.8-16.9 × 13.0- 19.6 mm, South Africa, Durban, 10-11.XI.1938, leg. H. Engel) have been deemed by Crosnier as suitable syntypes of his G. fourmanoiri. However, despite the Code ’s Recommendation (Art. 74E) about the verification of locality (“ When selecting a lectotype, the author should, if possible, verify the accuracy of the locality ascribed to it”), it is obvious that these two samples, RMNH D3250 from Durban and RMNH D3210 from Reunion Rocks, have not been collected from Nosy Bé, Madagascar by A. Crosnier. It is likely that they were only subsequently identified by him as G. fourmanoiri and, therefore, they cannot be considered syntypes, even if they correspond to G. fourmanoiri.Published as part of Ng, Ngan Kee, Rodríguez Moreno, Paula A., Naruse, Tohru, Guinot, Danièle & Mollaret, Noémy, 2019, Annotated type-catalogue of Brachyura (Crustacea, Decapoda) of the Muséum national d'Histoire naturelle, Paris. Part II. Gecarcinidae and Grapsidae (Thoracotremata, Grapsoidea), with an Appendix of pre- 1900 collectors, pp. 91-130 in Zoosystema 41 (7) on page 104, DOI: 10.5252/zoosystema2019v41a7, http://zenodo.org/record/372252
FIG. 16. — Thalamita auauensis dytica n in Portunidae (Crustacea, Decapoda, Brachyura) de Polynésie française, principalement des îles Marquises
No full textFIG. 16. — Thalamita auauensis dytica n. ssp., Seychelles, REVES II, stn 51, 3°52,5'S, 55°38,6'E, 45-60 m; A, ov. paratype 7,1 × 12,2 mm (MNHN-B 9155, en partie), carapace; B-D, holotype 6,4 × 9,8 mm (MNHN-B 9155, en partie); B, dents antérolatérales gauches; C, sixième segment abdominal et telson; D, partie distale du pléopode 1 gauche. Figure D d'après Crosnier 1984. Échelles: A, 2 mm; B, C, 1 mm; D, 0,1 mm.Published as part of Crosnier, Alain, 2002, Portunidae (Crustacea, Decapoda, Brachyura) de Polynésie française, principalement des îles Marquises, pp. 401-449 in Zoosystema 24 (2) on page 429, DOI: 10.5281/zenodo.540201
Mursia longispina Crosnier 1997
No full textMursia longispina Crosnier, 1997 MATERIAL EXAMINED. — SALOMON 2, stn CP 2284, 8°38.4’S, 157°21.5’E, Rendova, 195-197 m, XI.2004, 1 ♂ cl 40.0 mm, 1 ♀ cl 30.3 mm (MNHN B.30215). — Stn CP 2287, 8°40.84’S, 157°24.6’E, Rendova, 253-255 m, XI.2004, 2 ♂♂ cl 12.8 and 14.1 mm, 1 juv. (MNHN B.30216). DISTRIBUTION. — Previously known only from New Caledonia, 250-397 m (Crosnier 1997), new record for the Solomons. Genus Paracyclois Miers, 1886Published as part of Galil, Bella S., 2007, The deep-water Calappidae, Matutidae and Leucosiidae of the Solomon Islands, with a description of a new species of Euclosia Galil, 2003 (Crustacea, Decapoda, Brachyura), pp. 555-563 in Zoosystema 29 (3) on page 556, DOI: 10.5281/zenodo.468995
Hymenopenaeus chacei Crosnier & Forest 1969
No full text<i>Hymenopenaeus chacei</i> Crosnier & Forest, 1969 <p>(Fig. 3 A–B)</p> <p> <i>Hymenopenaeus chacei</i> Crosnier & Forest, 1969: 545, fig. 1–2.— Crosnier & Forest 1973: 261, fig. 82.— Cardoso <i>et al</i>. 2014:51.</p> <p> <b>Material examined.</b> 1 Female, Potiguar Basin, MT# 62, 410 m, 04° 47.83' S / 036° 11.02' W, 8 May 2011, MOUFPE: 16787. 8 individuals, 2 Males, 6 Females, Potiguar Basin, MT# 63, 416 m, 04° 36.24' S / 036° 45.75' W, 5 May 2011, MOUFPE: 16789. 2 individuals, 1 Male, 1 Female, Potiguar Basin, MT#75, 04° 28.80' S / 036° 52.55' W, 5 May 2011, MOUFPE: 16786. 1 Female, Potiguar Basin, MT#84-2, 2034 m, 04° 25.83' S / 036° 37.36' W, 5 July 2011, MOUFPE: 16791. 3 Females, Potiguar Basin, MT#85, 2068 m, 04° 21.35' S / 036° 44.27' W, 5 May 2011, MOUFPE: 16785.</p> <p> <b>Diagnosis.</b> The rostrum, straight, is directed slightly upwards, reaching the second segment of the antennal peduncle, with 6–7 teeth on rostrum, two post-rostral teeth unequal: the posterior presents at the base of dorsal margin a very small projection, bottom edge of rostrum smooth without teeth. Four spines acute in carapace antennal, rostral, hepatic and branchiostegal. Ocular peduncle longer than the width of the cornea. Abdome with somites 4–6 dorsally carinated. (Modified by Crosnier & Forest, 1969).</p> <p> <b>Geographic distribution.</b> (Fig. 4) Western Atlantic: Brazil (<b>Ceará</b> and <b>Rio Grande do Norte</b> - First report from southwestern Atlantic). Eastern Atlantic: Mid Atlantic Ridge, Portugal (Madeira Island), West Sahara, Morocco, Mauritanian, Senegal, Gabon, Bissau? Guinea, Guinea, Namibia (Crosnier & Forest 1969; 1973; Cardoso <i>et al</i>. 2014).</p> <p> <b>Bathymetric distribution.</b> The specimens of <i>H. chacei</i> have been collected in Potiguar Basin between the depths of 410–2068 m; however, their occurrence is usually between 750–1300 m (Crosnier & Forest 1969; 1973), thus extending its bathymetric distribution from deep waters.</p> <p> <b>Remarks.</b> The specimens analyzed herein do not differ from the description of Crosnier & Forest (1969) and Crosnier & Forest (1973). According to Crosnier & Forest (1973), the species of <i>Hymenopenaeus chacei</i> belongs to the group of genus <i>Hymenopenaeus</i> that doesn't have the pterygostomian spine, but the branchiostegal spine in the previous region, and showing two post-rostral teeth, which is formed by <i>H. propinquus</i> (de Man, 1907), <i>H</i>. <i>equalis</i> (Bate, 1888), <i>H</i>. <i>neptunus</i> (Bate, 1881), <i>H. obliquirostris</i> (Bate, 1881), <i>H</i>. <i>fattahi</i> Ramadan, 1938, <i>H</i>. <i>halli</i> Bruce, 1966, <i>H</i>. <i>debilis</i> Smith, 1882 and <i>H</i>. <i>aphoticus</i> Burkenroad, 1936. The specimens collected in this study indicated a wide bathymetric distribution of species, being collected between isobaths from 400 m to 2000 m along the continental slope. The species of <i>H. chacei</i> has a disjunct distribution, reported only from eastern Atlantic (Crosnier & Forest 1969; 1973) and from the Mid Atlantic Ridge reported by Cardoso <i>et al</i>. (2014), thus, this paper report the first occurrence of species from the southwestern Atlantic (Brazilian waters), filling gap along the Atlantic Ocean.</p>Published as part of <i>Alves-Júnior, Flavio De Almeida, Araújo, Marina De Sá Leitão Câmara De & Souza-Filho, Jesser F., 2017, New records of deep-sea shrimps of family Solenoceridae Wood-Mason & Alcock, 1891 (Crustacea: Decapoda: Dendrobranchiata) from Southwestern Atlantic, pp. 473-484 in Zootaxa 4254 (4)</i> on pages 476-478, DOI: 10.11646/zootaxa.4254.4.4, <a href="http://zenodo.org/record/556053">http://zenodo.org/record/556053</a>
Economie de l'immatériel : abondance, exclusion et biens communs
No full text@article{RN-LECROSNIER-2006, author = {Le Crosnier, H.}, title = {Economie de l'immatériel : abondance, exclusion et biens communs}, journal = {Hermès}, year = {2006}, pages = {51-59} }National audienc
L'évolution des modèles éditoriaux confrontés aux documents numériques
No full text@inbook{OL-LECROSNIER-2004, author = {Le Crosnier, H.}, title = {Publier sur Internet, séminaire INRIA, 27 septembre-1 octobre 2004, Aix Les Bains}, chapter = {L'évolution des modèles éditoriaux confrontés aux documents numériques}, publisher = {Ed. de l'ADBS}, year = {2004}, pages = {11-63}
Systellaspis curvispina Crosnier 1987
No full textSystellaspis curvispina Crosnier, 1987a (Fig. 33 A–C, 34) Systellaspis curvispina Crosnier, 1987a: 711, Figs. 6–8.—Crosnier 1987b: 957 (Key).— Lunina et al. 2018: 3, fig. 2 (Key). Systellaspis cristata Chace, 1986: 64 (Part), Fig. 35c. Material examined. 3 M and 2 F, Fernando de Noronha, Abracos 2 ST# 39/ Leg.2, Midwater Tow, 800 m, 04° 52,42’ S / 034° 3,51’ W; 04° 50,86’ S / 034° 5,11’ W, 24 April 2017, MOUFPE: 18.400. 1 OF, Rio Grande do Norte, Abracos 2 ST#35, Midwater Tow, 1150 m, 04° 36,48’ S / 035° 29,86’ W; 04° 18,54’ S / 035° 32,40’ W, 20 April 2017, MOUFPE: 18.439. 3 M and 4 F, Fernando de Noronha, Abracos 2 ST#40/ Leg. 2, Midwater Tow, 440 m, 03° 31,35’ S / 032° 31,63’ W; 03° 31,51’ S / 032° 31,67’ W, 24 April 2014, MOUFPE: 18.409. 2 F, Ceará Chain, Abracos 2 ST#52A/ leg. 2, Midwater Tow, 984 m, 03° 43,26’ S / 033° 25,15’ W; 03° 42,22’ S / 033° 35,82’ W, 0 2 May 2017, MOUFPE: 18.438. 1 F, Rocas Atoll, Abracos 2 ST# 53A/ Leg. 2, Midwater Tow, 610 m, 03° 48,99’ S / 033° 59,27’ W; 03° 50,05’ S / 033° 58,74 W, 0 2 May 2017, MOUFPE: 18.446. Diagnosis: Rostrum shorter than carapace with 10–13 dorsal teeth and 6–11 ventral teeth. Carapace with dorsal carina on posterior half of midline and with strong ventral carina and with lateral ridge extending from orbit to posterior margin. Abdomen with first somite bearing a blunt barb on anterior margin; Third abdominal somite with dorsal tooth with the tip directed upward. Telson with 20 or more dorsolateral spines (modified by Crosnier 1987a). Distribution: Western Atlantic: Brazil (Ceará Chain (seamount), Rio Grande do Norte and Fernando de Noronha Archipelago). Indo-Pacific Oceans: Madagascar, Philippines, Indonesia (Fig. 34). Bathymetric distribution: 140–500 m (Crosnier 1987), herein this species was found between 440–1150 m, thus extending its bathymetric distribution from deep waters. Remarks: According to Crosnier (1987a, b), S. curvispina is closely related to S. cristata Faxon, 1893, being slightly differentiated in (characters of S. cristata in parentheses): rostrum with 6–11 ventral teeth (vs. 5–8 ventral teeth); dorsal spine on third somite well developed with the tip directed upward (vs. dorsal spine on third somite well developed with the tip not directed upward). Until the present study, only two species of Systellaspis was known in Brazilian waters: S. debilis (A. Milne-Edwards, 1881) and S. pellucida (Filhol, 1885), however, these species differ by S. curvispina in the following way (character of S. debilis and S. pelucida respectively in parentheses): carapace with two sharp longitudinal lateral carinae (vs carinae absent) and rostrum with 10–13 dorsal teeth and 6–11 ventral teeth (vs 15 dorsal and 4–10 ventral teeth; vs 11 dorsal and 5 ventral teeth). Systellapsis curvispina was previously recorded only from Indo-Pacific Oceans (Fig. 34), with few records made by Crosnier (1987a, b) in mesopelagic zones. Thus, this paper comprises the first record of S. curvispina in Atlantic Ocean (Brazilian waters).Published as part of Alves-Júnior, Flavio De Almeida, Silva, Elinai Dos Santos, Araújo, Marina De Sá Leitão Câmara De, Cardoso, Irene, Bertrand, Arnaud & Souza-Filho, Jesser F., 2019, Taxonomy of deep-sea shrimps of the Superfamily Oplophoroidea Dana 1852 (Decapoda: Caridea) from Southwestern Atlantic, pp. 401-442 in Zootaxa 4613 (3) on pages 429-430, DOI: 10.11646/zootaxa.4613.3.1, http://zenodo.org/record/323976
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