Casmaria boblehmani, Fedosov & Olivera & Watkins & Barkalova, 2014
publication ID |
https://doi.org/ 10.5852/ejt.2014.78 |
publication LSID |
lsid:zoobank.org:pub:3C2942F0-9C88-4382-B28C-0F02D7200EA5 |
DOI |
https://doi.org/10.5281/zenodo.3851687 |
persistent identifier |
https://treatment.plazi.org/id/FA0142B4-BEF4-4F08-8BFD-C0870F39DC88 |
taxon LSID |
lsid:zoobank.org:act:FA0142B4-BEF4-4F08-8BFD-C0870F39DC88 |
treatment provided by |
Tatiana |
scientific name |
Casmaria boblehmani |
status |
sp. nov. |
Casmaria boblehmani View in CoL sp. nov.
urn:lsid:zoobank.org:act:FA0142B4-BEF4-4F08-8BFD-C0870F39DC88
Fig. 2 View Fig
Casmaria ponderosa View in CoL – Robin 2008: 145, fig. 5 — Buijse et al. 2013: 13, fig. 25-2 [middle specimen], pl. 6, figs 6, 8, 13, pl. 7, figs 1, 5, 8-10, 12-15, 17, pl. 8, fig. 1,?pl. 10, fig. 11.
Etymology
This species is named to honor I. Robert (Bob) Lehman, a great scientist, mentor and teacher. One of the authors (BMO) has been the grateful direct beneficiary of his remarkable generosity.
Type material
Holotype
Molecular voucher Casm.5, 36.3 mm, Danajon Banks, off Olango Island, Cebu, Philippines, 10°17.8’ N, 124°05.3’ E, 10-25 m, coll. local diver, Jun. 2012, ANSP-453749 ( Fig. 2A-C View Fig ). GoogleMaps
Paratypes
1 (35.1 mm) and 2 (34.8 mm, molecular voucher Casm. 7), same locality as holotype, ANSP-453750 ( Fig. 2D-E View Fig ). The holotype and paratype 2 provided the two DNA sequences labeled Casm. 7 and Casm. 5, respectively, in Fig. 1 View Fig .
Other material examined
PHILIPPINES: 34.6 mm, off Masbate Island, Central Philippines, coll. local diver, BO collection; 34.9 mm, off Calituban Island, Bohol, 9 m, on mud, BO collection; 44.9 mm, off Cuyo Island, Palawan, 10-25 m, BO collection; 32.2 mm, Palawan Island, unknown locality, 10-15 m, BO collection. AUSTRALIA: 27.7 x 18.8 mm, tip of Cape Yorke, Queensland, BO collection ( Fig. 2F View Fig ). INDONESIA: 38.6 x 25.4 mm, off Woka Island, Molucca Sea, BO collection ( Fig. 2G View Fig ). VANUATU: juv., Expedition “ SANTO 2006”, Stn. FR10, Belmoul Lagoon, 15°36.7’ S, 167°05.8’ E, 5-25 m, MNHN IM- 2007-33625; juv., Expedition “ SANTO 2006”, Stn. FR03, Belmoul Lagoon entrance, 15°36.2’ S, 167°06.3’ E, 3-32 m, MNHN IM- 2007-33628 ( Fig. 1A View Fig ). FIJI: 41.5 x 24.2 mm, off Akuilan Island, ANSP 276463 ( Fig. 2H-I View Fig ). SOCIETY ISLANDS: 36.5 x 24.6 mm, Atiue, Tahiti, ANSP 266122 ( Fig. 2K-L View Fig ).
Description
Adult shell small to medium-sized, solid, glossy, ovate-elongate with very prominent terminal varix, studied specimens 34.8-36.3 mm high. Proportions of shell vary considerably, ratio of shell breadth to height 0.58-0.7. Protoconch of about 4 smooth, evenly convex whorls. Teleoconch of 4-5 whorls; early spire whorls evenly convex, with no sculpture. Last adult whorl and in most specimens penultimate whorl with row of glossy nodules (6 to 12 on last whorl), weakly developed in some specimens ( Fig. 2D-E View Fig ), prominent in others ( Fig. 2 G View Fig ). Due to nodules, late whorls distinctly shouldered; shoulder situated at mid-height of penultimate whorl and adapical quarter of last adult whorl. Aperture ovate, outer lip strongly thickened, drawn upwards, with wide, shallow sinus in upper side. Interior of outer lip with distinct dentition. Apertural varix very prominent, thick, with ten brownish-black blotches on abapertural face; adapertural face with seven or eight well-developed spines directed transversally to apertural plane. Their positions correspond approximately with black blotches on abapertural face. Columellar shield solid, white, heavily callused, with numerous spiral wrinkles in some specimens. Last adult whorl of pinkish, tan, or pale brown background color, with indistinct brown spiral stripes and a row of brown to blackish-brown spots below suture. Siphonal canal with black blotch. Interior of aperture pale brown. Tip of protoconch brown.
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Remarks
Specimens that are most appropriately assigned to Casmaria boblehmani sp. nov. are found at sites in eastern Indonesia, northern Australia (Northern Territory and Queensland), Vanuatu and the South Pacific. The largest specimen (51.8 mm) that we can confidently assign to C. boblehmani sp. nov. is known from the Philippines ( Buijse et al. 2013: pl. 6, fig. 13). In the Philippines C. boblehmani sp. nov. occurs syntopically with C. ponderosa , C. erinaceus and C. turgida . All four species co-occur in sandy patches at depths of 1 to 30-40 meters.
Characters allowing the unequivocal recognition of Casmaria boblehmani sp. nov. and the delimitation of the Casmaria species described to date are summarized in Table 2 View Table 2 .
Casmaria ponderosa and C. boblehmani sp. nov. can be distinguished from each other by the number and arrangement of brown blotches on the dorsal side (abapertural face) of the terminal varix: C. ponderosa has five major blotches and two to three intermediate strokes, while C. boblehmani sp. nov. has nine to ten blotches of equal or subequal size, evenly distributed along the varix of most specimens. Another character, although less stable, is a row of spots on the shell base, posterior to the siphonal canal. These are always distinct in C. ponderosa , but are missing in most specimens, or in rare cases present but indistinct, in C. boblehmani sp. nov.
Specimens of Casmaria erinaceus can easily be distinguished from both C. ponderosa and C. boblehmani sp. nov. by the absence of dentition on the inner surface of the outer lip and by the presence of only three or four (very rarely five) spines restricted to the anterior edge of the outer lip, directed forward. The anterior edge of the outer lip is drawn slightly forward and abaxially. Both C. ponderosa and C. boblehmani sp. nov. have distinct dentition on the inner surface of the outer lip and have six or more spines directed transversely to the apertural plane, located along the anterior and medial edges of the outer lip. Most of these characters were mentioned by Abbott (1968) and Buijse et al. (2013) as allowing discrimination between C. erinaceus and C. ponderosa .
Casmaria boblehmani sp. nov. can be readily distinguished from Casmaria turgida (Reeve, 1848) . The latter species is rather conservative in morphology throughout its range ( Buijse et al. 2013) and has a shell with evenly convex whorls, notable because of the characteristic zigzag color pattern. Besides that, C. turgida exceeds all co-occurring Casmaria forms in size. Unfortunately, C. turgida is missing in our molecular dataset. However, the conservative morphology of this species and its sympatry on a small scale with C. erinaceus , C. ponderosa and C. boblehmani sp. nov. at a number of Indo-Pacific localities prove that it is a distinct species.
Despite the fact that C. ponderosa , C. boblehmani and C. turgida in most cases can be distinguished from each other confidently by the combination of characters discussed above, these characters may intergrade to a certain extent, creating somewhat intermediate forms that may be difficult to interpret. Buijse et al. (2013: pl. 6, figs 6, 8, pl. 9, fig. 15) depicted a few specimens of intermediate appearance that we are not certain where to assign. All these specimens have smooth shells intermediate between C. ponderosa and C. turgida in size (48-51 mm).
Among the other Casmaria species not occurring sympatrically with C. boblehmani sp. nov., C. unicolor (Pallary, 1926) is probably the most similar. As in other Casmaria species, C. unicolor varies significantly in sculpture and encompasses both smooth and nodulose forms, and the nodulose form closely resembles C. boblehmani sp. nov. (see Buijse et al. 2013: pl. 22). These two forms seem to differ in the number of spines on the outer lip. C. boblehmani sp. nov. possesses seven to eight spines, while C. unicolor has 10-12, and they are located along the entire length of the lip in many specimens, reaching the adapical angle of the aperture. Apart from that, C. unicolor can be distinguished by its more inflated upper (adapical) whorl profile and more clearly distinguished, weakly flattened sutural ramp, giving it a wider, more stepped spire outline. Casmaria unicolor is restricted to the Red Sea ( Fig. 3 View Fig ), and the widely distant distributions of this species and C. boblehmani sp. nov. suggest that these two forms are sufficiently divergent to be considered as separate species.
The three species Casmaria cernica (G. B. Sowerby III, 1888), C. perryi (Iredale, 1912) and C. atlantica Clench, 1944 are extremely similar to each other. They are characterized by being narrower in outline and with a narrower terminal varix than C. boblehmani sp. nov. Besides that, all three mentioned species share the same arrangement of dark blotches on the dorsal side of the apertural varix as in C. ponderosa : five major blotches with one or two intermediate strokes between each major pair.
In comparison with Casmaria boblehmani sp. nov., C. kalosmodix (Melvill, 1883) has a much larger, far more elongate and more narrowly varicate shell with narrow axial color lines that are not present in other Casmaria species, and with no spines on the outer lip. As in C. boblehmani sp. nov., the blotches on the abapertural face of the varix in C. kalosmodix are narrow, but in the latter species they are grouped in 3-4 clusters, separated by wide interspaces.
Another species, Casmaria kayae Buijse, Dekker & Verbinnen, 2013 , in general resembles C. erinaceus . C. boblehmani sp. nov. can easily be distinguished from C. kayae by the number and position of spines on the outer lip and by the color pattern. C. kayae has three or four (five in a few specimens) spines on the anterior portion of the lip, and these are directed forward. Many specimens have a distinctive zigzag color pattern, quite different from the usual coloration of C. boblehmani sp. nov.
Finally, C. beui Buijse, Dekker & Verbinnen, 2013 , from Western Indian Ocean, can easily be distinguished from C. boblehmani sp. nov. by its small size, its smooth, thin, relatively very wide shell with distinctively inflated whorls, and by its characteristic color pattern, resembling that of C. turgida .
Distribution
Casmaria boblehmani sp. nov. is widely distributed across the Pacific Ocean: from the Philippines, eastern Indonesia, northern Australia, to Fiji and the Society Islands, and (based on specimens illustrated by Buijse et al. 2013) to Hawaii ( Fig. 3 View Fig ). Possibly reaches India (based on the specimen illustrated by Robin 2008).
Species | Smooth form | Nodulose form | Number / direction of spines on OL | Position of spines on OL | Number of blotches on TV | Dentition within | Row of blotches at suture | Row of blotches on shell base | Color pattern | Individual characters |
---|---|---|---|---|---|---|---|---|---|---|
C. erinaceus | x | x | 3-5 / f | a 1/3 | 7-14 se | - | - | - | no, zigzags, spiral rows of dots | |
C. kayae | x | x | 3-5 / f | a 1/3 | 9-12 se | - | - | - | zigzags | |
C. ponderosa | x | x | 7-9 / tr | a 1/2 - 3/4 | 5 + 1-2 | + | + | + | no | |
C. turgida | x | - | 8-11 / tr | a 1/2 - 3/4 | 5 +1-2 or 10-11 se | - | + | - | zigzags | shell length usually exceeds 60 mm |
C. boblehmani | ? | x | 8-9 / tr | a 1/2 - 3/4 | 8-10 se | + | + | r | no, spiral bands | |
C. unicolor | x | x | 10-12 / tr | a 2/3 - 4/5 | 11-12 se | - | + | + (n.f.) | no, zigzags, spiral rows of dots | inflated upper whorl profile giving the shell a wider, more stepped spire outline |
C. cernica | x | - | 6-7 / tr | a 1/2 | 5 + 1-2 | - | + | + | spiral rows of blotches | narrow and narrowly varicate shell |
C. atlantica | x | - | 6-7 / tr | a 1/2 | 5 + 1-2 | - | + | - | spiral bands | narrow and narrowly varicate shell |
C. perryi | x | - | 6-7 / tr | a 1/2 | 5 + 1-2 | - | + | - | spiral bands | narrow and narrowly varicate shell |
C. beui | x | - | >9 | a 2/3 | 10-11 se | r | + | + | spiral rows of blotches, zigzags | shell very small, wide and thin |
C. kalosmodix | x | - | ?- | - | 5, 10-11 se | - | + | r | axial lines + spiral bands | narrow axial lines over entire shell surface |
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Kingdom |
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Class |
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Order |
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Genus |
Casmaria boblehmani
Fedosov, Alexander, Olivera, Baldomero M., Watkins, Maren & Barkalova, Varvara 2014 |
Casmaria ponderosa
Robin 2008: 145 , fig. 5 |
Buijse et al. 2013: 13 , fig. 25-2 [middle specimen], pl. 6, figs 6, 8, 13, pl. 7, figs 1, 5, 8-10, 12-15, 17, pl. 8, fig. 1,?pl. 10, fig. 11. |