Newmanella radiata ( Bruguiére, 1789 ), Bruguiere, 1789
publication ID |
https://doi.org/ 10.11646/zootaxa.4098.2.1 |
publication LSID |
lsid:zoobank.org:pub:B7622A1E-0781-4643-A72A-61A648B260D6 |
DOI |
https://doi.org/10.5281/zenodo.5632841 |
persistent identifier |
https://treatment.plazi.org/id/A37087A2-FFB7-FFB3-FF1A-FA9FFD81FE81 |
treatment provided by |
Plazi |
scientific name |
Newmanella radiata ( Bruguiére, 1789 ) |
status |
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Newmanella radiata ( Bruguiére, 1789)
Figures 2 View FIGURE 2 –8
Lepas indiae orientalis ex violaceo radiata Chemnitz, in Martini & Chemnitz, 1785: 319, pl. 99, fig. 842.
Balanus radiata Bruguiére, 1789: 168 .— Bruguiére 1789: pl. 164, figs 5, 5a.
Balanus radiatus .— Ranzani, 1818: 75.— Lamarck 1818: 393.— Ranzani 1820: 39.—Jay 1839: 7.
Conia radiata .— Blainville 1824: 378.— Blainville 1825: 598.—Blainville 1827: pl. 85, figs 5, 5a.
Tetraclita (Conia) radiata .— Gray 1825: 104.
Tetraclita radiata .— Darwin 1854: 343, pl. 11, figs 5, 5a.— Weltner 1897: 258.— Gruvel 1903: 161.— Gruvel 1905: 291.— Schmalz 1906: 65, pl. 6, fig. 4.— Hoek 1907: xvi.— Pilsbry 1916: 259, pl. 61.— Pilsbry 1927: 38.— Nilsson-Cantell 1939: 5.— Pope 1943: 244.— Pope 1945: 368.— Pilsbry 1953: 27.— Southward 1962: 163.— Ross 1968: 18.
Newmanella radiata .— Ross 1969: 242, figs 3, 4.— Ross & Perreault 1999: 2, 4.
Material examined. Neotype. SIO-BIC C12193. 1 specimen, near Turtle Rocks, Bimini, the Bahamas (1 Jul. 1967). Neoparatypes. SIO - BIC 12194-12198. 5 specimens, near Turtle Rocks, Bimini, the Bahamas (1 Jul. 1967). Other materials. SIO-C7218. 2 specimens, Vieques Sound, Puerto Rico, (19 Oct. 1966). SIO-C7218. 2 specimens, Vieques Sound, Puerto Rico, (19 Oct. 1966). C6056. 2 specimens, Margarita Is, Venezuela (28 May 1968). SIO- C7199. 3 specimens, Colon Bay, Panama (collection date unknown). SIO-C7204. 2 specimens, Vieques Sound, Puerto Rico (19 Oct. 1966). SIO-C7206. 1 specimen, Scotts Head Bay, Dominica (1 May 1966). C7207. 6 specimens, near Turtle Rocks, Bimini, the Bahamas (1 Jul. 1967). SIO-C7218. 2 specimens, Vieques Sound, Puerto Rico (19 Oct. 1966). C7231. 2 specimens, southern part of Gulf of Paria, midway between Trini (collection date unknown).
Diagnosis. Parietes white. Scutum with shallow lateral depressor muscle crests. Rami of cirrus II without triangular spines; basipods of cirri IV, V and VI with triangular spines. Fourth and fifth mandibular teeth adjacent. Maxillule with cutting margin below notch not protruding.
Description. Shell white, low conic; surface smooth with radiating lines ( Fig. 2 View FIGURE 2 A–C). Orifice pentagonal, diamond-shaped ( Fig. 2 View FIGURE 2 A–C); radii broad with horizontal striations, summits oblique; alae with summits less oblique than those of radii. Base of parietes with several rows of irregularly sized tubes, shell basis calcareous ( Fig. 2 View FIGURE 2 B). Scutum triangular, height similar to width ( Fig. 2 View FIGURE 2 D); dorsal surface with horizontal striations ( Fig. 2 View FIGURE 2 E); ventral surface with adductor ridge long, extending from basal margin to half height of tergum ( Fig. 2 View FIGURE 2 D. G); articular ridge and articular furrow narrow ( Fig. 2 View FIGURE 2 D); lateral scutal depressor muscle crests shallow ( Fig. 2 View FIGURE 2 D). Tergum triangular; longitudinal furrow on dorsal surface broad, shallow; spur narrow ( Fig. 2 View FIGURE 2 D, E) with faciole open, tip rounded ( Fig. 2 View FIGURE 2 E); articular ridge high, occupying almost 1/3 of scutum when articulated ( Fig. 2 View FIGURE 2 F), deep, wide ( Fig. 2 View FIGURE 2 D, G); area with lateral depressor muscle crests thin (Fig, 2D); scutal margin smooth, without conspicuous teeth ( Fig. 2 View FIGURE 2 D).
Cirrus I with unequal rami; posterior ramus (14-segmented) about 2/3 length of anterior rami (21-segmented) ( Fig. 3 View FIGURE 3 A); intermediate segment of posterior ramus protuberant ( Fig. 3 View FIGURE 3 B); segments of anterior ramus normal; lesser curvature of both rami without spines; setae on both rami serrulate ( Fig. 3 View FIGURE 3 C, D). Cirrus II with unequal rami; posterior ramus (16-segmented) about 1.5 length of anterior ramus (8-segmented) ( Fig. 3 View FIGURE 3 E); setae on both rami serrulate ( Fig. 3 View FIGURE 3 F, H); terminal segment of anterior ramus bearing a few bi-pinnate setae ( Fig. 3 View FIGURE 3 G); lesser curvatures of segments of both rami not bearing spines. Cirrus III with posterior ramus antenniform (19- segmented), about 1.5 times length of anterior ramus anterior (10-segmented) ( Fig. 4 View FIGURE 4 A); segments on lesser curvature of the both rami bearing triangular shaped spines ( Fig. 4 View FIGURE 4 B–D); lesser curvature of entire anterior ramus bearing hook-shaped triangular spines ( Fig. 4 View FIGURE 4 A) (observations from 6 specimens (SIO-C7207) from the Bahamas and 1 specimen (SIO-C7204) from Puerto Rico); posterior ramus with distal 3 segments not bearing hook-shaped spines ( Fig. 4 View FIGURE 4 A). Cirrus III with serrulate and bidentate setae ( Fig. 4 View FIGURE 4 E–H). Cirri IV–VI long, slender, anterior and posterior rami similar length ( Figs 5–6 View FIGURE 5 View FIGURE 6 ); basis of cirri IV–VI bearing triangular spines ( Figs 5 View FIGURE 5 B, C, 6B, E); greater curvature of proximal segment of anterior rami bearing triangular spines ( Fig. 5 View FIGURE 5 B, D, 6C, F). Cirrus IV, anterior ramus 22-segmented, posterior ramus 24-segmented ( Fig. 5 View FIGURE 5 A), lesser curvature of anterior ramus bearing triangular spines ( Fig. 5 View FIGURE 5 E–G). Cirrus V, anterior ramus 25- segmented, posterior 26-segmented ( Fig. 6 View FIGURE 6 A). Cirrus VI, anterior ramus 24 segmented, posterior ramus 25 segmented ( Fig. 6 View FIGURE 6 D). Cirrus IV with intermediate segments of both rami in bearing 2 pairs of long serrulate and 1 pair of short simple setae ( Fig. 5 View FIGURE 5 F, H). Intermediate segments of both rami of cirri V and VI bearing 3 pairs of long serrulate and 1 pair of short simple setae ( Fig. 6 View FIGURE 6 G, H). Penis basi-dorsal point absent; annulations along whole length; setae sparsely distributed ( Fig. 6 View FIGURE 6 I); tip with a few bundles of setae ( Fig. 6 View FIGURE 6 J).
Maxilla bi-lobate, taller than broad, serrulate setae on both lobes ( Fig. 7 View FIGURE 7 A, B), surface with short spines ( Fig. 7 View FIGURE 7 C). Maxillule with V-shaped notch, two large spines above notch, cutting margin below notch straight, with 10 large setae ( Fig. 7 View FIGURE 7 D-F). Mandible with 5 teeth ( Fig. 7 View FIGURE 7 G, H), first largest, separated from remainder, fifth smallest, located adjacent to fourth; second, third and fourth teeth bidentate, fourth with cutting edge serrated ( Fig. 7 View FIGURE 7 H); lower margin straight, with ~16 fine setae; inferior angle sharp ( Fig. 7 View FIGURE 7 H). Mandibulatory palp rectangular (Fig. 8A); serrulate setae on superior margin (Fig. 8B–D). Labrum with V-shaped notch (Fig. 8E–H), 5 large teeth on each side of cutting margin ( Fig. 7 View FIGURE 7 G, H);
Remarks. Newmanella radiata was originally named by Martini and Chemintz (1785) in a non-binomial name as Lepas indiae orientalis ex violaceo radiata . Bruguiére (1789) was the first to give the binomial name Balanus radiata and mentioned the habitat as the Indian Ocean, but did not mention a type locality. There is no information on the deposition of any type specimens of Balanus radiata . Ross (1969) revised the Tetraclitidae and erected Newmanella , assigning Newmanella radiata as the type species and concluding that the distribution of N. radiata is from Florida to the Caribbean Sea in the Atlantic Ocean. In the present study, we record a species of Newmanella from the Pacific that is morphologically close to N. radiata described by Ross (1969) from the Caribbean. Without setting up a neotype for N. radiata , the taxonomic status of N. radiata is unstable. Any Newmanella species collected in the Pacific and Atlantic Oceans, which are similar to the shell and opercular illustrations in Bruguiére (1789), can be identified as N. radiata , as there is no type specimen and no type locality for comparison. It is, therefore, essential to designate a neotype for N. radiata to facilitate further taxonomic comparisons of morphologically close species. The present study follows the suggestion of Ross (1969) that N. radiata is confined to the Caribbean waters, selecting a specimen of N. radiata collected from Bimini in the Bahamas as the neotype.
Detailed descriptions of Newmanella radiata are scarce. Most previous literature (e.g. Bruguiére 1789; Darwin 1854; Schmalz 1906; Pilsbry 1916) described N. radiata based on shells and opercular plates (scutum and tergum). Ross (1969) was the first to provide descriptions and drawings of soft parts (cirri, penis and mouth parts) of N. radiata collected from the Caribbean. The present study further illustrates the detailed morphology of N. radiata for comparative taxonomic studies.
SIO |
Scripps Institution of Oceanography |
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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Newmanella radiata ( Bruguiére, 1789 )
Chan, Benny K. K. & Cheang, Chi Chiu 2016 |
Newmanella radiata
Ross 1999: 2 |
Ross 1969: 242 |
Tetraclita radiata
Ross 1968: 18 |
Southward 1962: 163 |
Pilsbry 1953: 27 |
Pope 1945: 368 |
Pope 1943: 244 |
Nilsson-Cantell 1939: 5 |
Pilsbry 1927: 38 |
Pilsbry 1916: 259 |
Schmalz 1906: 65 |
Gruvel 1905: 291 |
Gruvel 1903: 161 |
Weltner 1897: 258 |
Darwin 1854: 343 |
Tetraclita (Conia) radiata
Gray 1825: 104 |
Conia radiata
Blainville 1825: 598 |
Blainville 1824: 378 |
Balanus radiatus
Ranzani 1820: 39 |
Ranzani 1818: 75 |
Lamarck 1818: 393 |
Balanus radiata Bruguiére, 1789 : 168
Bruguiere 1789: 168 |
Lepas indiae orientalis
Martini 1785: 319 |