Journal of Threatened Taxa | www.threatenedtaxa.org | 26 June 2026 | 18(6): 29120–29126

 

ISSN 0974-7907 (Online) | ISSN 0974-7893 (Print) 

https://doi.org/10.11609/jott.10328.18.6.29120-29126

#10328 | Received 23 December 2025 | Final received 25 March 2026| Finally accepted 18 May 2026

 

 

An evasive naticid surfaces in India: first confirmed report of Gennaeosinum perobliquum (Dautzenberg & Fischer, 1907) (Gastropoda: Naticidae)  

 

Aparna Mishra 1, Sanjaya Dalai 2, Roberto Ardovini 3, N.V. Subba Rao 4  & Dipti Raut 5         

 

1,2,5 Centre of Excellence in Environment and Public Health, Environmental Science Laboratory, Department of Zoology, Ravenshaw University, Cuttack, Odisha 753003, India.

3 Department of Information Technology, ITIS FERMI ROMA Technical Institute, Rome 00135, Italy.

4 Molluscan Section, Zoological Survey of India, New Alipore, Kolkata, West Bengal 700053, India.

1 aparnamishra839@gmail.com, 2 s.dalai1996@gmail.com, 3 roberto_ardovini@fastwebnet.it, 4 subbarao_nalluri@hotmail.com, 5 diptiraut@ravenshawuniversity.ac.in (corresponding author)

 

 

Editor: Han Raven, Naturalis Biodiversity Center, Leiden, Netherlands.                   Date of publication: 26 June 2026 (online & print)

 

Citation: Mishra, A., S. Dalai, R. Ardovini, N.V.S. Rao & D. Raut (2026). An evasive naticid surfaces in India: first confirmed report of Gennaeosinum perobliquum (Dautzenberg & Fischer, 1907) (Gastropoda: Naticidae). Journal of Threatened Taxa 18(6): 29120–29126. https://doi.org/10.11609/jott.10328.18.6.29120-29126

  

Copyright: © Mishra et al. 2026. Creative Commons Attribution 4.0 International License. JoTT allows unrestricted use, reproduction, and distribution of this article in any medium by providing adequate credit to the author(s) and the source of publication.

 

Funding: The first author AM acknowledges the financial research support provided by the Council of Scientific &

                 Industrial Research, New Delhi, India (File no. 09/1036(24086)/2025EMR-1 dated 13/10/2025).

 

Competing interests: The authors declare no competing interests.

 

Author details: Aparna Mishra: a Ph.D research scholar with research interest in benthic ecology and focus on molluscan taxonomy. Sanjaya Dalai: a Ph.D research scholar with research interest in benthic ecology and focus on molluscan taxonomy. Roberto Ardovini: professor at ITIS Fermi Roma (Technical Institute of Information Technology, Rome), specializing in malacology and conchology, with a focus on the taxonomy and description of marine gastropods and bivalves. His work includes descriptions of new species and contributions to global shell inventories. N.V. Subba Rao: scientist and Former Head of the Molluscan Section, Zoological Survey of India. Expertise in the taxonomy, systematics, and faunal documentation of Indian molluscs across marine, freshwater, and terrestrial habitats. Landmark works are foundational reference material for Indian malacology. Dipti Raut: professor of Zoology at Ravenshaw University, Cuttack, Odisha, India. Research focuses on macrobenthic Community ecology. Work integrates environmental monitoring with Marine biodiversity documentation.

 

Author contribution: Conceptualization: Dipti Raut, N. V. Subba Rao; Methodology: Dipti Raut, Aparna Mishra, Sanjaya Dalai; Data Collection: Sanjaya Dalai, Aparna Mishra, Roberto Ardovini; Data Analysis: Aparna Mishra, Sanjaya Dalai, Roberto Ardovini; Writing Original Draft: Aparna Mishra, Sanjaya Dalai; Writing Review and Editing: Dipti Raut, N. V. Subba Rao, Roberto Ardovini; Supervision: Dipti Raut

 

Acknowledgments: The first author AM acknowledging the financial research support provided by the Council of Scientific & Industrial Research, New Delhi, India (File no. 09/1036(24086)/2025EMR-1 dated 13/10/2025). The authors are thankful to the Department of Zoology, Ravenshaw University, Cuttack, Odisha, India, for the laboratory facilities. The anonymous reviewerscomments greatly improved the manuscript. 

 

 

Abstract: This study provides the first record of the naticid species Gennaeosinum perobliquum in Indian waters.  Previously documented from Vietnam, Indonesia, and South Africa, G. perobliquum was collected during a benthic survey, from the intertidal zone of Chandipur, Balasore, Odisha, on the eastern coast of India.  A clear description of the shell morphology is provided, along with detailed morphometric and imaging analyses. By comparing G. perobliquum with related naticid species found in India, this work aims to refine taxonomic understanding and contribute to knowledge of naticid biodiversity in the region. This newly documented record not only expands the known geographic distribution of G. perobliquum but also underscores the importance of continued benthic faunal surveys for further exploration of molluscan biodiversity in the Bay of Bengal and adjacent regions.

 

Keywords: Bay of Bengal, benthos, Chandipur, first record, geographic distribution, Indian waters, intertidal, mollusc biodiversity, moon shells, Odisha.

 

Abbreviation: TSL—Total Shell Length | WB—Width of the last whorl | HB—Height of the last whorl | SL—Spire Length | CL—Columella Length | UL—Length of the Umbilical callus | (AW)a—Aperture Width towards anterior side | (AW)b—Aperture Width towards posterior side | dd—Dead specimen | RZEVB—Ravenshaw University Zoology Environmental Science Budhabalanga Estuary | ZSI M—Zoological Survey of India Mollusca.

 

 

Introduction

 

Members of the cosmopolitan family Naticidae within the phylum Mollusca and class Gastropoda inhabit a wide range of environments, from intertidal to the deep sea. Commonly called moon shells, these oval-shaped predatory gastropods are known for their distinctive drilling behavior, which they use to prey on various bivalves and gastropods.  They typically dwell in sandy and muddy substrates, where they remain hidden (Huelsken et al. 2008). The Naticidae family includes four subfamilies, 38 genera, and about 260–270 species (Kabat 1996; WoRMS 2025).

The genus Gennaeosinum Iredale, 1929, comprises three valid species. Kilburn (1976) classified it as a subgenus of Eunaticina; Gennaeosinum is consistently characterized by a thick funicle, a feature absent in all Eunaticina species. Although 36 Naticidae species across 12 genera have been documented in India, no Gennaeosinum species has been reported from the region (Tripathy et al. 2024). This study documents the first record of Gennaeosinum perobliquum (Dautzenberg & Fischer, 1907) in the Bay of Bengal, expanding its known distribution.    Gennaeosinum perobliquum was described initially from “Ben-Son” (probably Binh Son, south of Da Nang) in Vietnam (Dautzenberg & Fischer 1907) and later recorded from Durban, Kwazulu-Natal, South Africa (Kilburn 1976) and Indonesia (Bakker et al. 2026). This species is often misidentified as Eunaticina papilla (Gmelin, 1791) due to similar spiral lirae patterns. As detailed here, G. perobliquum can be reliably distinguished from Eunaticina species occurring in India.

A recent study (Mishra et al. 2024) identified the naticid Sinum laevigatum (Lamarck, 1822) along Odisha’s coast, underscoring the need for further research on Naticidae in this region. Consequently, extensive surveys were conducted along Odisha’s entire coastline, with particular focus on the intertidal zone of Chandipur, where specimens were collected.

This study not only adds G. perobliquum to the list of species known in Indian waters but also highlights the rich malacofaunal diversity present along the largely unexplored eastern coast of India. It provides a thorough examination of the specimen, including the holotype description and comparative analyses with closely related species, aiming to mitigate future taxonomic ambiguities. Enhanced photographic documentation and detailed morphometric measurements are included to enrich the understanding of shell sculpture and address existing gaps in the literature.

 

Materials and Methods

 

A survey was conducted in the Chandipur intertidal region (21.455° N, 87.045° E) (Figure 1) during September 2025. Samples were randomly collected during low tide by hand-picking and stored; dead specimens were placed in ziplock pouches, and live specimens were preserved in 4% formalin. Dead specimens were carefully washed, air-dried, and sorted. Sediment samples were obtained through manual excavation using a hand shovel for the purpose of analyzing soil texture. Morphometric measurements were obtained using a dial caliper (Safeseed, China; resolution 0.1 mm, accuracy ± 0.2 mm), while shell surface structures were examined under a stereo microscope (Leica E24W, Germany). Specimen photographs were captured with a Nikon Z 30 camera (MC 50 mm / 2.8 f). Following vouchering, specimens were deposited in the Environmental Science Laboratory, Department of Zoology, Ravenshaw University, Cuttack, Odisha, India.

Morphological identification was performed based on the holotype description (Dautzenberg & Fischer 1907), supplemented by additional information from Kilburn (1976). A critical comparison was made with other naticids reported from India, as documented by Rao (2003). The taxonomic status was verified through the World Register of Marine Species (WoRMS 2025).

 

 

Result

 

Systematics

Family: Naticidae Guilding, 1834

Subfamily: Sininae Woodring, 1928

Genus: Gennaeosinum Iredale, 1929

Type species: Gennaeosinum peleum Iredale, 1929 (type by original designation)

 

Gennaeosinum perobliquum (Dautzenberg & H. Fischer, 1907) (Image 1A–H)

Chresonomy

Sigaretus (Eunaticina) perobliquus Dautzenberg & H. Fischer, 1907:  p. 178, pl. 5, figures 4–5.

Eunaticina papilla (non Gmelin); Kensley, 1973: 93, fig. 323.

Eunaticina (Gennaeosinum) perobliqua (Dautzenberg & Fischer, 1907) - Kilburn 1976; p. 872, figure. 22 (c).

Eunaticina (Gennaeosinum) perobliqua (Dautzenberg & Fischer, 1907) - Bakker H, Gill A, Creuwels J (2026). Naturalis Biodiversity Center (NL) - Mollusca. Naturalis Biodiversity Center. Occurrence dataset https://doi.org/10.15468/yefvnk accessed via GBIF.org on 2026-05-05. https://www.gbif.org/occurrence/2444340122.

Type Locality: “Ben-Son” (probably Binh Son, south of Da Nang) in northern Vietnam

IUCN status: Not Evaluated.

Material examined: Two specimens (dd), Accession number: RZEVB18 (TSL 13.5 mm, WB 10.2 mm); RZEVB19 (TSL 13.9 mm, WB  10.5 mm) were examined from the Chandipur intertidal, Balasore, Odisha, eastern coast of India (21.455° N, 87.045° E), coll.  Sanjaya Dalai & Aparna Mishra.

Additional material studied: Figured type material of Sigaretus (Eunaticina) perobliquus Dautzenberg & Fischer, 1907 (images examined from Dautzenberg & Fischer 1907; p. 178, pl. 5, figure 4–5).

Topotype of Eunaticina papilla (Gmelin, 1791) (Zoological Survey of India, Registration number ZSI M 22150/4).

Specimen of Eunaticina linnaeana (Récluz, 1843) (Zoological Survey of India, Kolkata, Registration number M25925/5).

Description: Shell solid, white, moderately elongated oval; aperture strongly prosocline. Low, depressed spire with blunt tip; deep suture. Protoconch slightly convex, smooth, glossy white with brown tinge; two whorls. Transition to teleoconch not well defined; feeble spiral ribs present. Teleoconch with two whorls, last whorl highly convex much larger than previous whorls. Teleoconch surface initially smooth, later marked by strong arc-like growth lines; faint spiral ribs becoming distinct and unevenly distributed on last whorl. Around 9–10 spiral ribs on penultimate whorl, separated by shallow, broad interspaces. Ribs more elevated below suture, flattening with lower interspaces on last whorl. Spiral ribs become denser towards base; growth lines become stronger towards outer lip. Spiral threads continue into inner side of umbilical groove. Aperture semicircular, wider anteriorly. Inner lip almost straight, slight concavity towards parietal region; anterior region curved. Thick parietal callus extends over umbilicus, forming a funicle that covers umbilicus backwardly. Funicle divided by shallow groove. Wide open anteriorly, deep umbilical groove. Operculum corneous.

Remarks: A thick callus pad covers the umbilical groove and the funicle, which has a shallow groove that divides it into two. These are the key identification features that confirm the first report of the genus Gennaeosinum and the species G. perobliquum from India. The multi-spiral protoconch with two whorls signifies a planktonic veliger larval stage (Vendetti, 2007). This developmental form implies improved dispersal abilities; therefore a large distribution area is to be expected.

Distribution: From Vietnam (Holotype) through Indonesia (GBIF) and India to South Africa (Kilburn, 1976) (Figure 2).

Locality within India: Chandipur Intertidal, Balasore, Odisha, east coast of India, present study (Figure 2).

Habitat: The species has repeatedly been recorded from shallow water. Chandipur’s intertidal stretch shows diverse sedimentary conditions, with a silty mudflat in the middle region. The upper intertidal region has a coarse, sandy substratum, encompassing high diversity.

 

 

Discussion

 

Identification of Naticidae can be challenging because of their highly cryptic morphology and very minor interspecific variation (Sharma et al. 2021). In India, three genera of the Sininae subfamily are represented: Eunaticina P. Fischer, 1885, Sigatica O. Meyer & Aldrich, 1886, Sinum Röding, 1798. The genus Gennaeosinum herein reported is the fourth, represented by a single species. The aforementioned three genera are unique in several ways. Eunaticina differs from Sinum by its auricular, more depressed shape and wider aperture.  Gennaeosinum is similar to Eunaticina and was treated as its subgenus by Kilburn (1976). Gennaeosinum is differentiated from Eunaticina by a thick callus pad in the parietal region, which is absent in Eunaticina. Gennaeosinum includes three species: G. intercisum Iredale, 1931, G. peleum Iredale, 1929, and G. perobliquum (Dautzenberg & Fischer, 1907). Kilburn included several other species, namely G. kraussi (E.A. Smith, 1902) and G. linguifera Thiele, 1925, but now G. kraussi is accepted as Eunaticina kraussi whereas G. linguifera is accepted as Natica Linguifera. This work confirmed the first report of the Gennaeosinum genus and the species G. perobliquum from Indian marine waters. Previously, this species was found in the western and central Indo-Pacific regions. It now extends its range into the Bay of Bengal. There are few descriptions or images of the species besides the original description, which has excellent figures. Kilburn (1976) did not provide an illustration. The Indian specimens align with the original description and Kilburn’s description of the features of the South African specimen.

The species can be confused with two Eunaticina species well known from the Indo-West Pacific: E. papilla (Gmelin, 1791) and E. linnaeana (Récluz, 1843). Kilburn (1976) compared G. perobliquum with E. linnaeana, but the specimens are more similar to E. papilla. Eunaticina linnaeana is larger and broadly ovate, while G. perobliquum is smaller and moderately ovate. Both have low spires, but the conical shape distinguishes the latter. Eunaticina linnaeana has fine spiral grooves, whereas G. perobliquum is ornamented with well-developed, flat spiral ribs.  Eunaticina linnaeana has an aperture that is wider, elongated, and larger, giving it a distinct look compared to the semicircular opening in G. perobliquum. Eunaticina linnaeana has frequently been misidentified as E. papilla, leading to similar confusion with G. perobliquum. E. papilla has an exserted spire, shallow suture, and ovate aperture. G. perobliquum resembles E. papilla in size, spiral ribs, and moderately large aperture. Distinctively, G. perobliquum stands out from both Eunaticina species because it features a thick callus pad in the parietal region, divided into two by a shallow groove, a feature always absents in Eunaticina.

Various factors influence the dispersal of naticid species in Indian marine waters. Oceanic currents and ballast water from ships play a major role (Ruiz et al. 2000; Cowen & Sponaugle 2009; Treml et al. 2015). The Bay of Bengal, located in the northern Indian Ocean, shares environmental and habitat characteristics with the central and western Indo-Pacific marine regions. These include high sea surface temperatures, a variety of coastal and open-water habitats, and rich biodiversity, all characteristic of tropical Indo-West Pacific ecosystems (Spalding et al. 2007).  Climate change and rising sea temperatures are likely to shift the ecological niches of these species. This could extend their distribution beyond previously established ranges (Wallingford & Sorte 2022; Lin et al. 2024). Changes in species distribution may be hard to establish due to a lack of comprehensive surveys and challenges in species identification, especially given the cryptic nature of Gennaeosinum perobliquum (D’Souza & Shenoy 2023).  Research on the Naticidae family in India has been limited, particularly along the eastern coast. This highlights the need for further exploration, including the collection of live specimens and the establishment of a DNA database to elucidate intraspecific and interspecific relationships among Indian naticid species.

 

 

Conclusion 

 

The discovery of G. perobliquum underscores significant connections among molluscan fauna in the Indo-West Pacific and highlights the urgent need for a comprehensive taxonomic review of naticid species in India. This study also confirms the limited exploration of malacofaunal diversity along the eastern coast. Additionally, this record expands the regional species list and deepens the understanding of biogeographical patterns in the Indo-West Pacific. These findings are crucial for developing effective conservation strategies and for protecting biodiversity in the region.

 

 

Table 1. Morphometrics of Gennaeosinum perobliquum collected from Odisha.

Specimen

TSL

WB

HB

SL

CL

UL

(AW)a

(AW)p

RZEVB18

13.5

10.2

7.8

3.8

11.3

4.0

6.8

3.9

RZEVB19

13.9

10.5

8.9

3.9

11.0

3.8

7.4

4.3

 

For figures & image - - click here for full PDF

 

References

 

Bakker, H., A. Gill & J. Creuwels (2026). Naturalis Biodiversity Center (NL) — Mollusca. Naturalis Biodiversity Center. Occurrence dataset https://doi.org/10.15468/yefvnk. Accessed on 05.x.2026. https://www.gbif.org/occurrence/2444340122.

Cowen, R.K. & S. Sponaugle (2009). Larval dispersal and marine population connectivity. Annual Review of Marine Science, 1: 443–466.

D’Souza, S.L. & K.B. Shenoy (2023). Marine molluscs of India-a review on their diversity and distribution. Journal of Coastal Conservation 27(6): 67. https://doi.org/10.1007/s11852-023-00998-0

Dautzenberg, P. & H. Fischer (1907). Contribution à la faune malacologique de l’Indo-Chine. Journal de Conchyliologie 54(3): 145–226.  https://biodiversitylibrary.org/page/16298507

Huelsken, T., C. Marek, S. Schreiber, I. Schmidt & M. Hollmann (2008). The Naticidae (Mollusca: Gastropoda) of Giglio Island (Tuscany, Italy): Shell characters, live animals, and a molecular analysis of egg masses. Zootaxa 1770(1): 1–140. https://doi.org/10.11646/zootaxa.1770.1.1

Kabat, A.R. (1996). Biogeography of the genera of Naticidae (Gastropoda) in the Indo-Pacific. American Malacological Bulletin 12(1): 29–35.

Kensley, B. (1973). Sea-shells of Southern Africa. Gastropods. Maskew Miller, Cape Town, 225 pp.

Kilburn, R.N. (1976).  A revision of the Naticidae of Southern Africa and Moçambique (Mollusca). Annals of the Natal Museum 22(3): 829–884.

Lin, X.N., C.Y. Ma, L.S. Hu, M.L. Liao, L.X. Ma, P.R. Teske, A. Hoffmann & Y.W. Dong (2024). Genomics-informed range predictions under global warming reveal reduced adaptive diversity whilst buffering range shifts for a marine snail.  Global Change Biology 30(11): e17571. https://doi.org/10.1111/gcb.17571

Mishra, A., S. Dalai, R. Behera, N.V.S. Rao & D. Raut (2024). Rare Moon Shell Sinum laevigatum (Gastropoda: Naticidae): a new record from coastal waters of peninsular India. Thalassas 40: 653–657. https://doi.org/10.1007/s41208-023-00652-4

Rao N.V.S. (2003). Indian Seashells (Part-I): Polyplacophora and Gastropoda. Records of Zoological Survey of India Occasional Paper 192: 1–416.

Ruiz, G.M., J.T. Carlton, E.D. Grosholz & A.H. Hines (2000). Invasion of coastal marine communities in North America: apparent patterns, processes, and biases. Annual Review of Ecology and Systematics 31: 481–531.

Sharma, N., S. Mondal, S.S. Das, K. Bose & S. Saha (2021). Morphological conservatism of the family Naticidae (Gastropoda) through time: potential causes and consequences. Paleobiology 47(3): 487–502. https://doi.org/10.1017/pab.2020.62

Spalding, M.D., H.E. Fox, G.R. Allen, N. Davidson, Z.A. Ferdaña, M. Finlayson, B.S. Halpern, M.A. Jorge, A. Lombana, S.A. Lourie, K.D. Martin, E. McManus, J. Molnar, C.A. Recchia & J. Robertson (2007). Marine ecoregions of the world: a bioregionalization of coastal and shelf Areas. BioScience 57(7): 573–583. https://doi.org/10.1641/B570707

Treml, E.A., J.J. Roberts, Y. Chao, P.N. Halpin, H.P. Possingham & C. Riginos (2015). Reproductive output and duration of the pelagic larval stage determine population connectivity in the Indo-Pacific. Biological Conservation 187: 249–257.

Tripathy, B., P.C. Tudu, A. Mukhopadhyay, S.K. Sajan, C.R. Sreeraj, S.D. Gurumayum, A. Ghosh, R. Sultana, J. Purushothaman & A. Siddique (2024).  Checklist of Fauna of India: Mollusca.  Version 1.0.  Zoological Survey of India.  https://doi.org/10.26515/Fauna/1/2023/Mollusca

Vendetti, J.E. (2007). Protoconch comparative morphology in extinct and extant buccinid gastropods and its utility in paleobiogeography, systematics, and inferring larval mode. Malacologist 48: 1–5.

Wallingford, P.D. & C.J.B. Sorte (2022). Dynamic species interactions associated with the range-shifting marine gastropod Mexacanthina lugubrisOecologia 198: 749–761. https://doi.org/10.1007/s00442-022-05128-5

WoRMS Editorial Board (2025). World Register of Marine Species. Available from https://www.marinespecies.org at VLIZ. Accessed on 10.x.2025. https://doi.org/10.14284/170