Siphonaria delicata, Jenkins, Bruce & Köhler, Frank, 2024
publication ID |
https://doi.org/10.11646/megataxa.13.1.1 |
DOI |
https://doi.org/10.5281/zenodo.14989347 |
persistent identifier |
https://treatment.plazi.org/id/0D49832F-FF0E-8288-FF68-FA42FE63FD76 |
treatment provided by |
Plazi (2025-03-05 09:04:49, last updated 2025-03-07 14:54:03) |
scientific name |
Siphonaria delicata |
status |
sp. nov. |
Siphonaria delicata View in CoL sp. nov.
( Figs 56A–C, M View FIGURE 56 , 58C–D View FIGURE 58 )
Material examined. Type material. Holotype, from Ethel Beach 10°27.827’S, 105°42.497’E, Christmas Is, Indian Ocean; coll. B.W. Jenkins, CI02-1, 11 Sept 2018 ( AM C.585322 [M421, SK108], Fig. 56A View FIGURE 56 ). GoogleMaps
Five paratypes, same data as holotype ( AM C.585585 2p, WAM S74043 p, WAM S74041 p [M307], Fig. 56C View FIGURE 56 , WAM S74042 p [M410], AM C.608199 p [SK093], Fig. 56B View FIGURE 56 ) GoogleMaps .
External morphology. Animal evenly pale cream without any dark/black pigmentation; paler at foot/ wall edge; mantle wider than foot wall, weakly lobed, translucent, covers exposed inner shell lip, outer edge thickened; genital pore indistinct, located on foot wall to right anterior of right cephalic fold; two small black epithelial eye spots centralised on two centrally touching cephalic folds; pneumostomal lobe long, under the mantle, unpigmented, between the right ADMs.
Shell ( Figs 56A–C View FIGURE 56 ; Table S9). size small (max sl mean = 8.5 mm SD = 1.0 mm, n = 4), ovate, shell thin translucent; tall, apex offset to posterior; protoconch below height of apex, direction heterostrophic (n = 2), protoconch area distinctly dark brown to black; anterior apical side convex, posterior side concave, lateral apical sides straight to weakly concave; growth lines prominent; rib count (mean = 29.3, SD = 4.8, n = 3) primary ribs pale to dark grey, weakly raised, secondary ribs not prominent, 1–2 between primary ribs, rib interstices dark brown to black; siphonal ridge not prominent, shell lip even, weakly corrugated with some primary rib ridges; interior polished, shell lip apically banded with white rays aligning with primary ribs extending and narrowing over shell margin and ADM scar to the start of dark chocolate brown spatula; CMS weakly concave, similar but darker colouration to spatula and shell margin; thickening of inner shell lip occurs in larger specimens, resulting in white coating covering the brown/black colouration of inner shell lip.
Reproductive system ( Fig. 58C; n View FIGURE 58 = 2). Positioned within entire right side of coelom, against foot wall on foot muscle, under the respiratory cavity occupying large proportion of animal body volume. GA, EG and ED positioned between BM and RAM. GA small, with singular GP through foot wall; AO distinct, bluntly pointed, maybe elongated, joined to upper GA alongside ED; ED long, broad, centrally bent, joins to side of GA; GA, AO, ED all white muscular fibrous tissue; EG medium, soft whitish tissue, slightly folded, joins ED; single very long flagellum (F1), similar length and width to ED, appears as an extension of ED, possible F2. BD and CD with opposing connections into GA between ED join and GP, CD short,; BD long, both ducts smooth, thickened, whitish, featureless, pass closely together through RAM ( BD over CD) into soft white folded tissues of MG; MG / AG complex relatively large; BC embedded in folds close to embedded SV; BD with distal loop(s) and MA, longer thinner than CD; BC relatively large, spherical, thin whitish translucent test; HD short, wide, coiled, links ducts in soft white folded tissues of AG to small, yellowish granulated HG; outer edge of MG lobbed; AG larger than HG, both left outer sides curved to curvature of inner foot wall.
Spermatophore ( Fig. 58D View FIGURE 58 ). Test thin, translucent (length = 5.77 ± 1.23 mm, n = 2); over half-length comprises a translucent cylindrical head section (head length = 4.73 ± 0.79 mm, ~ 49% of SPM length, n = 3); tip bluntly rounded, containing a white gelatinous core mass; tapers into a filamentous transparent flagellum; head section much thicker than flagellum (head width = 59 ± 1.2 μm, flagellum width = 11 ± 0 μm, n = 3), both sections smooth, featureless; 6 and 3 SPM each in holotype and paratype.
Comparative remarks. In our mitochondrial phylogeny, S. delicata sp. nov. ( plicata group, unit 62) is the sister species of S. christmasensis sp. nov. ( Figs 1 View FIGURE 1 , 3 View FIGURE 3 ). Both differ from each other by COI distances of ≥ 10.7% (Table S7). For comparison with S. christmasensis sp. nov. refer to comparative remarks under that species. We found this species in sympatry with four other congeners on CI: For comparisons with S. alba , and S. incerta refer to comparative remarks under these species. Siphonaria tenebrae sp. nov. has a lower, darker shell with greater edge scalloping and raised ribbing, a smaller AO and BC, and a shorter ED. Siphonaria umbra sp. nov. has a slightly larger, taller shell with a dual-ribbed siphonal ridge, a shorter ED, and a slightly shorter SPM.
Distribution and habitat. Known only from CI, Australia, and likely endemic to this island ( Fig. 55 View FIGURE 55 ). In this study, found in sheltered positions on exposed rocky shores, at upper littoral level ( Fig. 56M View FIGURE 56 ).
Etymology. From ‘delicata’ (Latin = delicate) for the small, delicate shell; adjective.
FIGURE 1. Maximum Likelihood phylogram based on analyses of a concatenated sequence data set of 16S and COI. Branches are collapsed at the species level. Branch labels give unit numbers and accepted species names. Numbers on branches indicate branch support employing 10,000 ultrafast bootstraps.Available genus-group names are shown next to their type species. Scale bar indicating modelled sequence divergence.
FIGURE 3. Maximum Likelihood phylogram (partial, species not collapsed). Clades J–L (laciniosa and plicata groups) of the tree shown in Fig. 1. Branch labels give specimen identifiers for new sequences or Genbank accession numbers for imported sequences from other studies and geographic regions (see Tables S1–S2 for details). Identical haplotypes are merged into single tips. Numbers on branches indicate branch support by employing 10,000 ultrafast bootstraps. Clade names give unit numbers and accepted species names. Scale bar indicating modelled sequence divergence.
FIGURE 55. Known occurrence records of S. camura sp. nov., S. caubianensis sp. nov., S. christmasensis sp. nov., S. costellata sp. nov., S. delicata sp. nov., S. forticosta sp. nov. and S. gemina sp. nov.
FIGURE 56. Shells of S. delicata sp. nov., S. forticosta sp. nov., S. gemina sp. nov. A–C, M. S. delicata sp. nov., CI, Ethel Beach. A. Holotype AM C.585322 [M421, SK108]. B. Paratype AM C608199 [SK093]. C. Paratype WAM S74041 [M307]. M. In situ. D–F, P. S. forticosta sp. nov., Timor-Leste, Dili. D. Holotype AM C.584829 [M441]. E. Paratype AM C.585318 [SK546]. F. Paratype AM C.584825 [M445]. P. Protoconch, AM C.584830 [SK228]. G–T. S. gemina sp. nov. G. NT, Darwin, holotype AM C.585485 [M088]. H. NT, Cox Peninsula, paratype AM C.585487 [M089]. Q. NT, protoconch,AM C.585337 [SK088]. S. Darwin, animal. T. Darwin, in situ. I–J, N. Mauritius, North Albion. I. AM C.584971 [M249]. J. AM C.584972 [M250]. N. In situ. K–L, O, R. CKI. K. WAM S74044 [M317]. L. AM C.584849 [M315]. O. Animal. R. In situ. Scale bars 5 mm.
FIGURE 58. Reproductive morphology of S. costellata sp. nov., S. delicata sp. nov., S. forticosta sp. nov. and S. gemina sp. nov. A–B. Holotype of S. costellata sp. nov. ZRC.MOL.24890 [M416, SK100], Singapore, Lazarus Is. C–D. Paratype of S. delicata sp. nov. AM C.608199 [SK093], CI. E. Holotype of S. forticosta sp. nov. AM C.584829 [M441, SK227], Timor-Leste, Dili. F. S. forticosta sp. nov., AM C.585991 [SK547]. G–H. Holotype of S. gemina sp. nov. AM C.585485 [M088], NT, Darwin. I–J. S. gemina sp. nov., Mauritius AM C.584971 [M249]. Unlabelled scale bars 1 mm.
AM |
Australian Museum |
BM |
Bristol Museum |
GP |
Instituto de Geociencias, Universidade de Sao Paulo |
MG |
Museum of Zoology |
SPM |
Sabah Parks |
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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