The Bahamian Archipelago is a region with high diversity of marine molluscs (Redfern 2001; Redfern 2013). It is considered a distinct biogeographic subprovince referring to molluscs (within the Caribbean province), with high levels of micro-speciation and endemism because of the disjunct arrangement of separate malacofaunas in the over 8000 islands and coral cays that compose it (Petuch 2013). The micro-speciation phenomenon is particularly evident in groups with non-planktotrophic development (Ornelas-Gatdula et al. 2011; Ornelas-Gatdula and Valdés 2012), especially when studied as a whole in the area (Caballer et al. 2014). The high rate of endemism observed may be the result of the isolation, caused by extensive open areas of “sterile” sands, which act as ecological barriers (Petuch 2013), or it may be explained by post-recruitment ecological factors, or historic vicariance (Ornelas-Gatdula and Valdés 2012; Carmona et al. 2014).

Ornelas-Gatdula and Valdés (2012) and Malaquias (2014) published a brief overview on the biogeography of the Bahamas and on the connectivity between the diverse regions of the Caribbean. These authors pointed out the existence of genetically distinct clades in this subprovince for some groups of molluscs, despite the general faunal homogeneity of the Caribbean. Moreover, Malaquias (2014) remarked the importance of the Bahamas for the biodiversity of the whole tropical western Atlantic region and discussed that the archipelago may “act as a centre of origination of new species”. In addition, it seems common in certain families of heterobranchs to observe a distribution pattern comprising an endemic species from the Bahamas that is sister to a widespread western Atlantic species living in the same kind of habitat, suggesting an allopatric speciation process (Carmona et al. 2014).

Spurilla dupontae Carmona, Lei, Pola, Gosliner, Valdés & Cervera, (2014) is a species of aeolidacean mollusc described as being endemic to the Bahamas. In the latest morphological and molecular phylogeny of the genus provided by Carmona et al. (2014), it was found to be a sister taxa to a species from the eastern Atlantic (also see Carmona et al. 2013), whose taxonomical identity has been discussed by Ortea and Caballer (2014). The abnormal speciation pattern of both species led Carmona et al. (2014) to suggest that there is no universal explanation for the origin of the endemic heterobranch fauna of the Bahamas.

In this paper, S. dupontae, to date considered endemic to the Bahamas, is recorded for the first time in the Caribbean subprovince.

The only specimen of S. dupontae was collected by direct search during a scuba dive. It was photographed alive on its environment, then examined onshore, photographed in an aquarium and preserved in 98 % ethanol.

Carmona et al. (2014) studied the genus Spurilla Bergh, 1864 in depth, and concluded “that coloration is one of the main diagnostic traits for the five species” of the genus, “although some display substantial colour pattern variation”. These authors also established the distribution of the western Atlantic species: S. dupontae and Spurilla sargassicola Bergh, 1871 inhabit the Bahamas, and Spurilla braziliana MacFarland, 1909, the only representative of Spurilla in the Caribbean.

Carmona et al. (2014) observed "an intriguing combination of widespread species and endemics with restricted ranges" for the members of the genus Spurilla, while some recent papers on heterobranch sea slugs published by Ornelas-Gatdula et al. (2011), Ornelas-Gatdula and Valdés (2012), Carmona et al. (2013), proved the presence of some new cryptic species in the Bahamas not known in the Caribbean subprovince. In this context, it seemed logical to assume that S. dupontae was endemic to the Bahamas, as Carmona et al. (2014: 150) did. But the specimen of S. dupontae found in Martinique matches exactly on the original description of the species, and it is easy to distinguish from S. braziliana and S. sargassicola by the conspicuous reticulate pattern covering the body, and specially the rhinophores.

Since its original description, there has not been any records to S. dupontae in the Caribbean or anywhere else, but S. sargassicola, which shows certain similarities with S. dupontae, has been cited by Caballer et al. (2015) in Venezuela. This specimen from the southern end of the Caribbean, was collected on Caulerpa spp. and the illustration provided by Caballer et al. (2015: 5 E) shows an animal with a reticulate pattern that seem to include the rhinophores, thus, this record could be, indeed, attributed to S. dupontae. On the other hand, the Guadeloupe Archipelago is very close to Martinique, and nearer to the Bahamas. However, S. dupontae has not been captured there, not even after the intensive expeditions performed by the Muséum national d’Histoire naturelle (Paris) in 2012, which permitted a wide study of the sea slug fauna from the Archipelago (Ortea et al. 2012; Ortea et al. 2013; Caballer and Ortea 2014; Caballer and Ortea 2015) and the capture its congener S. braziliana (as S. neapolitana).

It has been stated that the Bahamas and the Turks and Caicos Islands are a special region in the western Atlantic, largely isolated from the Caribbean, except for minor exchange from the north coast of Cuba and Haiti (Cowen et al. 2006). The presence of S. dupontae in the Caribbean subprovince (even when scarce), implies that planktotrophy is the most probable way of development for this species, and suggests that there may be more gene flow between the Bahamas and the Lesser Antilles than that predicted by the model owed to Galindo et al. (2006).

In synthesis, further collections of S. dupontae are necessary to learn its real distribution in the Caribbean Province and to determine if its presence in Martinique is incidental or if the species is really established in the Island.