2urn:lsid:arphahub.com:pub:45048D35-BB1D-5CE8-9668-537E44BD4C7Eurn:lsid:zoobank.org:pub:91BD42D4-90F1-4B45-9350-EEF175B1727AZooKeysZK1313-29891313-2970Pensoft Publishers10.3897/zookeys.1143.8442784427Research ArticleCephalopodaMolluscaNautilidaeConservation BiologyTaxonomyCenozoicAmerican SamoaFijiPacific OceanVanuatuThree new species of Nautilus Linnaeus, 1758 (Mollusca, Cephalopoda) from the Coral Sea and South PacificBarordGregory J.gjbarord@gmail.comhttps://orcid.org/0000-0002-4482-80161ConceptualizationWriting - original draftWriting - review and editingData curationFormal analysisInvestigationMethodologyProject administrationResourcesSupervisionValidationVisualizationComboschDavid J.23Writing - review and editingData curationFormal analysisFunding acquisitionMethodologyResourcesValidationVisualizationGiribetGonzalohttps://orcid.org/0000-0002-5467-84293ConceptualizationWriting - review and editingData curationFunding acquisitionInvestigationMethodologyProject administrationResourcesValidationVisualizationLandmanNeilhttps://orcid.org/0000-0003-0038-80794Writing - review and editingData curationLemerSarah23Writing - review and editingData curationFormal analysisFunding acquisitionMethodologyResourcesValidationVisualizationVelosoJob5Writing - review and editingInvestigationMethodologyWardPeter D.5ConceptualizationWriting - original draftWriting - review and editingData curationFormal analysisFunding acquisitionInvestigationMethodologyProject administrationResourcesSupervisionValidationVisualizationDepartment of Marine Science, Central Campus, Des Moines, Iowa, USADepartment of Marine Science, Central CampusDes MoinesUnited States of AmericaMarine Laboratory, University of Guam, Mangilao, Guam, USAHarvard UniversityCambridgeUnited States of AmericaMuseum of Comparative Zoology & Department of Organismic and Evolutionary Biology, Harvard University, Cambridge, MA, USAUniversity of GuamMangilaoGuamDivision of Paleontology, American Museum of Natural History, New York, NY, USAAmerican Museum of Natural HistoryNew YorkUnited States of AmericaBiology Department, University of Washington, Seattle, WA, USAUniversity of WashingtonSeattleUnited States of America
Corresponding author: Gregory J. Barord (gjbarord@gmail.com)
Academic editor: Jiri Frank
20232501202311435169A64DE90C-D449-5F72-837F-67059A1AC528A98491CA-FA8F-45E1-BBD4-33C6628693A875752281704202222122022Gregory J. Barord, David J. Combosch, Gonzalo Giribet, Neil Landman, Sarah Lemer, Job Veloso, Peter D. WardThis is an open access article distributed under the terms of the Creative Commons Attribution License (CC BY 4.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.http://zoobank.org/A98491CA-FA8F-45E1-BBD4-33C6628693A8
Nautiloids are a charismatic group of marine molluscs best known for their rich fossil record, but today they are restricted to a handful of species in the family Nautilidae from around the Coral Triangle. Recent genetic work has shown a disconnect between traditional species, originally defined on shell characters, but now with new findings from genetic structure of various Nautilus populations. Here, three new species of Nautilus from the Coral Sea and South Pacific region are formally named using observations of shell and soft anatomical data augmented by genetic information: N.samoaensissp. nov. (from American Samoa), N.vitiensissp. nov. (from Fiji), and N.vanuatuensissp. nov. (from Vanuatu). The formal naming of these three species is timely considering the new and recently published information on genetic structure, geographic occurrence, and new morphological characters, including color patterns of shell and soft part morphology of hood, and will aid in managing these possibly endangered animals. As recently proposed from genetic analyses, there is a strong geographic component affecting taxonomy, with the new species coming from larger island groups that are separated by at least 200 km of deep water (greater than 800 m) from other Nautilus populations and potential habitats. Nautilid shells implode at depths greater than 800 m and depth therefore acts as a biogeographical barrier separating these species. This isolation, coupled with the unique, endemic species in each locale, are important considerations for the conservation management of the extant Nautilus species and populations.
Barord GJ, Combosch DJ, Giribet G, Landman N, Lemer S, Veloso J, Ward PD (2023) Three new species of Nautilus Linnaeus, 1758 (Mollusca, Cephalopoda) from the Coral Sea and South Pacific. ZooKeys 1143: 51–69. https://doi.org/10.3897/zookeys.1143.84427
Introduction
During the mid-19th century period of active study of nautilus taxonomy, little was known about their natural history or even the number of species of extant Nautilus Linnaeus, 1758. From the 1980s onward, diverse research concerning the biology and taxonomy of living nautiluses, including aspects of reproduction, inter- and intraspecific variation in shell morphology, distribution, and genetic variation, has shed light on this charismatic clade (Saunders 1981, 1987; Saunders and Landman 1987; Ward 1987; Woodruff et al. 1987; Wray et al. 1995; Bonacum et al. 2011; Kröger et al. 2011; Sinclair et al. 2011; Vandepas et al. 2016; Ward et al. 2016; Combosch et al. 2017; Zhang et al. 2021). This research has profoundly changed Nautilus taxonomy and significantly reduced the number of recognized species, often based on single specimens found in Australian waters and otherwise without provenance (Saunders 1987; Ward 1987). It further revealed that there are far more shell characters that can be utilized for taxonomy than previously realized. For example, Ward (1987) cited differences in shell coloration and shell size at maturity, proposing that Nautilus populations from Vanuatu and Fiji were sufficiently dissimilar to the type of N.pompilius Linnaeus, 1758 to warrant taxonomic differentiation. However, no new species or subspecies were formally defined in that publication.
The number of valid species accepted in the genus Nautilus has remained unsettled, even as new genetic information has added to our understanding of the variability within and between Nautilus species. Currently, the species that have been described are differentiated based upon their geographic habitat, including the three species described here (Fig. 1).
Geographic range map of Nautilus and Allonautilus.
https://binary.pensoft.net/fig/800678
The three “universally” accepted modern nautilid species of 21st century taxonomists are Nautiluspompilius (the type species), N.macromphalus G.B. Sowerby II, 1849, and N.stenomphalus G.B. Sowerby II, 1849. A fourth, N.belauensis Saunders, 1981, has been disputed, and is not currently supported by phylogenetic studies; it does not show significant morphological differences from all other extant species (Vandepas et al. 2016; Combosch et al. 2017; Tajika et al. 2021). It has been placed as a junior synonym of the type N.pompilius by Vandepas et al. (2016) but accepted as a valid species elsewhere (e.g., Jereb 2005). Similarly, controversial has been the acceptance of Nautilusrepertus Iredale, 1944, which genetic studies have linked with N.belauensis (Vandepas et al. 2016; Combosch et al. 2017; Saunders et al. 2017; Tajika et al. 2021), and which is currently considered a taxon inquirendum (WoRMS 2021). Additionally, the type designation for N.pompilius was recently designated to come from a neotype in Ambon, Indonesia (Nikolaeva et al. 2015), which most significantly brings into question the validity of N.pompilius in the Philippines, where a subspecies has already been described by Habe and Okutani (1988) as N.pompiliussuluensis. However, recent genome-wide genetic studies did not distinguish this (a single) Indonesian sample from the Philippine Nautilus population (Combosch et.al 2017). Future work on the relationship of these two range populations of Nautilus would surely improve our understanding of their genetic relationships.
Another significant taxonomic change in Nautilus systematics was the definition of the new genus Allonautilus (Ward and Saunders 1997). From the time of its first description, Nautilusscrobiculatus Lightfoot, 1786 was recognized to be morphologically different from all other nautiluses in shell shape, shell ornament, and shell coloration. However, with the first collection of living specimens of this taxon (Saunders and Davis 1985), significant differences in shell ultrastructure (the presence of a thick periostracum anatomically dissimilar to the homologous layer in all other extant nautilids), and anatomical and color differences of the fleshy hood were demonstrated. Later, dissection of preserved specimens revealed further differences from known species of Nautilus in the respiratory and reproductive systems (Ward and Saunders 1997). In consequence, Nautilusscrobiculatus, was removed from Nautilus and designated instead as the type species of a new genus, Allonautilus Ward & Saunders, 1997. Genetic studies (Wray et al. 1995; Sinclair et al. 2007; Bonacum et al. 2011; Sinclair et al. 2011; Vandepas et al. 2016; Combosch et al. 2017) have since confirmed significant genetic differences between A.scrobiculatus and the various other species placed in Nautilus, further supporting the designation (Bonacum et al. 2011; Vandepas et al. 2016; Combosch et al. 2017; Tajika et al. 2021).
Early phylogenetic studies based predominantly or exclusively on mitochondrial DNA data indicated major problems with conchological-defined Nautilus species and instead identified three geographically distinct clades (Bonacum et al. 2011; Vandepas et al. 2016) and concluded that most Nautilus species may not be valid. The subsequent application of genome-wide RAD-Seq data (Combosch et al. 2017) greatly increased the phylogenetic resolution among and within these three major clades and confirmed the presence of genetically distinct subclades among South Pacific Islands in New Caledonia (N.macromphalus), Vanuatu (N.vanuatuensis sp. nov.), Fiji (N.vitiensis sp. nov.), and American Samoa (N.samoaensis sp. nov.), of which the three latter species are described further in this paper. Interestingly, some phylogenetic analyses by Combosch et al. (2017) indicated significant genetic differences between Fiji and American Samoa, while a population genetic analysis (STRUCTURE) did not (Fig. 2), which may have been due to the limited sample size from both locations. Ongoing follow-up analyses using expanded datasets and recently generated genome assemblies (Zhang et al. 2021; Huang et al. 2022) will further clarify species boundaries and provide additional population genetic insights into the drivers of differentiation among island populations.
Phylogenetic relationships of nautilids based on maximum-likelihood analysis of 18,595 concatenated SNPs with IQtree as in Combosch et al. (2017). Numbers on nodes indicate ultrafast bootstrap resampling percentages (>50) based on 1000 replicates–asterisks indicate full support (* = 100%). Bootstraps values were replaced on intraclade nodes as follows: “-” for bootstraps values >50 – <90, “+” for bootstrap values ≥90. Colors correspond to geographic populations as indicated in the map on the bottom left. Species other than Nautiluspompilius are indicated by name at the tip of the tree. The STRUCTURE plots show the posterior probability for individual assignments of samples to different genetic clusters in clade-specific analyses. Distinct colors indicate different genetic clusters as inferred by STRUCTURE (not populations as on the tree and map).
https://binary.pensoft.net/fig/800679
In parallel with the various genetic studies, ecological observations of Nautilus populations have been undertaken (Saunders 1984; Dunstan et al. 2011a; Barord et al. 2014; Ward et al. 2016), including understanding of maximum habitat depths imposed by shell implosion of juveniles and adults. Coupled with the lack of planktonic dispersal of newly hatched nautiluses (Ward 1987), this indicated the potential for geographic isolation of populations surrounded by water depth deeper than implosion depths of 800 m and, thus, the potential for allopatric speciation. The behavior of adult nautiluses observed through ultrasonic tracking (Carlson et al. 1984; Ward et al. 1984; Dunstan et al. 2011b; Ward et al. 2016) is consistent with the hypothesis that nautiluses have limited dispersal ability.
The work of Combosch et al. (2017) provided genome-wide evidence consistent with the view that geographic distances and depths readily crossed by invertebrates and vertebrates with planktonic larval stages are effective barriers to migration for nautiluses. Our new mapping of Nautilus and Allonautilus populations (Fig. 1) with observable morphological differences as well as information from genetic studies suggest that 200 km of deep water (800 m or greater) between separated populations is sufficient to effectively prevent gene flow. These results documenting the genomic structure in Nautilus populations living on the isolated archipelagos of American Samoa, Fiji, and Vanuatu, as well as new morphological information presented below, led to the conclusion that the nautiluses at each of these archipelagos are part of distinct populations recognized as new species. While three of these have heretofore been placed in N.pompilius (e.g., Ward et al. 1977; Saunders 1987; Ward 1987; Woodruff et al. 1987; Bonacum et al. 2011), in this paper we define each as a new species of Nautilus, based on shell characters and hood morphology as well as previously published genome-wide population genetics results.
Materials and methods
We use a combination of previously published data, as well as measurements from both museum collections and from newly collected specimens to produce the complete character assemblage data presented here. The combination of morphological characters included: shell coiling descriptors, shell ornament, umbilicus, and hood morphology. One aspect of extant shell morphology that has not been used at the species level is shell decoration, including pattern, pigment hue, and percent of shell covered by pigment. Ward (1987) proposed that the latter (as viewed from the side) was more variable between species than within species and was the basis of the proposal that various species at the time accepted as N.pompilius in American Samoa, Fiji, and Vanuatu could be discriminated from the types by their different percentages of pigment cover. Here we use the percent of the shell covered with pigment, as viewed from the side, modified from the methods introduced by Ward (1987). When combined with other characters, pigment cover becomes useful for species level distinction. Specifically, we combine pigment cover with size at maturity. Shell color pattern as a discriminative character was separately presented by Ward (1987), who listed data taken from photographs of captured specimens, and then measured with a manual planimeter. We use essentially the same method here but use the far more discriminating software, ImageJ. In both cases, however, the photographs with the shell striping percentage of a side view of the entire shell was manually obtained using the NIH ImageJ program to separately measure the area of the entire shell, and then measuring that area from a side view that was pigmented, by manually tracing each stripe with the “Irregular circular area” tool. The patterns and the actual area of shell they were compared to (which excluded the area under the black region beneath the hood, and the umbilical region), is shown in Fig. 3.
Example of method used to determine percentage of pigmentation on lateral portion of shell in N.samoaensis sp. nov.
https://binary.pensoft.net/fig/800680
Additionally, a new character used here for species-level definition and useful for interspecies discrimination is mean shell diameter of mature specimens, as in Ward (1987) and Saunders (1987). All measures presented here come from photographs of either empty shells that are part of museum collections or living animals that were photographed and soon after released. In some cases, photographs and videos were also obtained from Nautilus populations in American Samoa, Fiji, and Vanuatu using baited remote underwater video systems (BRUVS) as described by Dunstan et al. (2011a) and Barord et al. (2014). Shell sizes were taken from various sources where size measurements were presented; these sources are listed in the captions of the various diagrams portraying the measured data.
Taxonomic sectionClass Cephalopoda Cuvier, 1795
Order Ectocochliata Schwartz, 1894
Subclass Nautiloidea Agassiz, 1847
Family Nautilidae de Blainville, 1825
Genus Nautilus Linnaeus, 1758AnimaliaEctocochliataNautilidaeA4119753-6D32-5E5C-A67F-31D43FBE31FENautiluspompiliusLinnaeus, 1758 (type species of Nautilus)Diagnosis
(emended from Saunders et al. 2017). Shell compressed and involute, mature shell size of 140–220 mm mean diameter; 21% pigment coloration; umbilical callus always present. Sexual dimorphism prominent in mature animals: males larger, with a broader aperture than females. Growth lines sinuous, with ocular and hyponomic sinuses well developed in mature shells. Shell surface details from smooth to finely reticulate, because of minute parallel, serial scallops on growth lines in some isolated populations and species. Shell coloration variable, with brown, reddish- to purple-brown, irregular single and bifurcating stripes lacking on the body chamber at maturity. Two discrete color morphs found: stripes continue from venter to umbilicus, and stripes stop at mid flank, with a prominent white patch, sometimes with pale tan color, surrounding umbilicus. Hood covered with flat, white, warty protuberances, with two prominent white ridges extending down midline of hood. Anatomical aspects of the type species recently detailed by Shigeno et al. (2010).
Discussion.
A key note from the recent work of Saunders et al. (2017) was dedicated to coloration. In that paper, the explicit statement of there being two color-pattern morphs as a character defining N.pompilius was made. While this is found in the types of N.pompilius from Ambon, as well as in the new species we define here from Fiji, it is not known from N.belauensis, N.macromphalus, or N.vanuatuensis, whereas color stripes to the umbilicus are not known from N.repertus or N.stenomphalus. We thus feel justified in proposing this as but one more useful, species-level character when combined with other characters. Here we have used photographs published by Saunders et al. (2017) as means of measuring the percent coloration of the newly defined type species of N.pompilius.
Holotype: accessioned at University of South Pacific Marine Station (USPMS) #12232 (Fig. 4). Collected from Suva Harbour, Fiji, 18°07'10.2"S, 178°24'45.0"E, at depths between 250 and 300 m on 30 Jul. 2018.
Lateral view of Nautilusvitiensis sp. nov., holotype USPMS #12232.
https://binary.pensoft.net/fig/800681Diagnosis.
The following characteristics distinguish Nautilusvitiensis sp. nov. from other species within the genus Nautilus: 15–30% pigment coloration on shell, more than in N.pompilius and less than in the other species described here; two color pattern morphs present, with both full (stripes from venter to umbilicus) and “umbilical white patch” variety, where stripes flowing down from venter stop short of umbilical region; shell color patterns composed of simple stripes beginning at venter and then extending down the side of shell; these are large and unbranched and are among the simplest of all nautilus shell coloration patterns. The largest specimens of the new species are smaller than the smallest mature N.pompilius, and this species is in general smaller than the other two new species described here, but there is certain overlap.
Description.
Nautiliconic, shell with umbilical plug, whorl higher than broad at maturity. Periostracum entirely absent in mature and near mature specimens; shell surface ornamented with growth lines parallel to apertural shape; no cross-hatching or ornament perpendicular to growth lines; low rugae. Hood morphology consists of low, elliptical white protuberances barely projecting above hood surface on either side of two long, raised, parallel white stripes running centrally down hood from shell whorl to aperture. White protuberances found between stripes on the entire central section (see hood details on Suppl. material 1: video 1; Fig. 7). Mean diameter of adult shell 149.3 mm, s.d. 7.548 (see range of measured specimens in Table 1).
Descriptive statistics of mature shell diameters measured of each of the three new species described as well as N.pompilius from the type locality at Ambon, Indonesia.
N.pompilius
N.vitiensis sp. nov.
N.samoaensis sp. nov.
N.vanuatuensis sp. nov.
N
28
35
10
18
Minimum (mm)
187
137
162
150
Maximum (mm)
207
165
177
163
Range (mm)
20
28
15
13
Mean
195.6
149.3
181.2
156.6
Std. deviation
5.144
7.548
5.029
5.237
Std. error
0.9721
1.276
1.590
1.234
Etymology.
The specific epithet, an adjective, refers to the type locality, the island of Viti Levu, Fiji, where the type specimen plus additional released specimens sampled for genetic work were collected.
Habitat and distribution.
Nautilusvitiensis sp. nov. inhabits areas along the coast of Viti Levu, Fiji at Suva Harbour and Pacific Harbour. Specimens were collected and filmed (Suppl. material 1: video 1) at depths between 200–400 m (Tajika et al. 2022).
Holotype: accessioned at the Natural History Museum, Smithsonian Institution, USNM 816658 (Fig. 5a). Collected in Taema Bank, American Samoa, 14°16'32.27"S, 170°41'12.58"W, between depths of 280 and 310 m on 22 July 1986. Paratypes: accessioned at Natural History Museum, Smithsonian Institution, USNM 816708 (Fig. 5b), same collecting data as holotype. Accessioned at American Museum of Natural History, AMNH 81945, same collecting data as holotype.
Lateral view of N.samoaensis sp. nov. A holotype USNM 816658 B paratype USNM 816708.
https://binary.pensoft.net/fig/800682Diagnosis.
The following characteristics distinguish Nautilussamoaensis sp. nov. from other species within the genus Nautilus: 32–36% pigment coloration, more than Nautilusvitiensis sp. nov. and less than Nautilusvanuatuensis sp. nov.; composed of stripes beginning at venter and then curving around in an arc pointing toward aperture as they finally intersect with umbilical region. As noted by Saunders et al. (1989), there is a faint, growth-line sized pattern of annual rings similar in scale and morphology to that found in Nautilusbelauensis, but far less marked. Shell color pattern most unique of all Nautilus species composed of multiple, branching stripes that have a rearward projection after descending from venter. No other known Nautilus species shows this color pattern, and shells are recognized because of this unique coloration pattern, coloration percentage, and shell shape like N.pompilius.
Description.
Nautiliconic, shell with umbilical plug, whorl higher than broad at maturity. Periostracum entirely absent in mature and near-mature specimens. Shell striping with a series of concentric circles that overlap in a way unique to this species, with a single exception, although this has been referred to as a “zigzag” pattern elsewhere. White protuberances found between stripes and outside of stripes on the entire central section (see hood details in Suppl. material 2: video 2; Fig. 7). Average shell diameter 171.3, s.d. 5.029 (see range of measured specimens in Table 1).
Remarks.
A single shell described and illustrated by Saunders et al. (1989) shows an identical pattern to that seen on every observed specimen of Nautilussamoaensis sp. nov., but that specimen (USNM 816705) is said to have come from Fiji. However, in the many Fijian nautilus shells with published figures, or examined by us, there has never been another with this pattern, nor has there ever been a shell of this size found in Fiji, so this specimen may have been mislabeled.
The color in freshly caught animals and as viewed underwater has a more magenta hue than is seen in dried shells from this locality. This has not been quantified, however, and as in all other known species, the color changes after the shell dries, red hues are lost, and the shell acquires a uniform brown color.
Etymology.
The specific epithet, an adjective, refers to the type locality, American Samoa.
Habitat and distribution.
Nautilussamoaensis sp. nov. inhabits areas near Pago Pago, American Samoa. Specimens were collected and filmed (Suppl. material 2: video 2) at depths between 200 and 400 m.
Holotype: accessioned at American Museum of Natural History, AMNH 131861 (Fig. 6a). Collected from Mele Bay, Port Vila, Vanuatu, 17°43'21.61"S, 168°16'01.98"E, at a depth of 185 m on 20 July 2004. Paratypes: accessioned at American Museum of Natural History, AMNH 131856 (Fig. 6b), same collecting data as holotype.
Lateral view of Nautilusvanuatuensis sp. nov. A holotype AMNH 131861 B paratype AMNH 131856.
https://binary.pensoft.net/fig/800683Diagnosis.
The following characteristics distinguish Nautilusvanuatuensis sp. nov. from other species within the genus Nautilus: 40–50% shell coloration, more than any other Nautilus species with a plugged umbilicus; pigmentation always composed of stripes extending from venter to umbilicus (no specimens show the “white patch” coloration of N.pompilius or N.vitiensis sp. nov.). This species is most similar in size, color pattern, and degree of shell covered by pigment to N.macromphalus, but the umbilical plug is always missing in the latter species.
Description.
Nautiliconic, shell with umbilical plug, whorl higher than broad at maturity. Periostracum entirely absent in mature and even near-mature specimens. Shell surface ornamented with growth lines parallel to apertural shape. No cross-hatching or ornament perpendicular to growth lines. Hood morphology consisting of low, elliptical white protuberances barely projecting above hood surface on either side of two long, raised, parallel white stripes running centrally down hood from shell whorl to aperture. White protuberances found between stripes on entire central section; they are low and non-digitate at their terminal ends (see hood details on Suppl. material 3: video 3; Fig. 7). Mean diameter of adult shell is 156.6 mm, s.d. 5.237 (see range of measured specimens in Table 1).
Underwater photos of living NautilusA, BN.samoaensis sp. nov. CN.vanuatuensis sp. nov. DN.vitiensis sp. nov.
https://binary.pensoft.net/fig/800684Discussion.
Nautilusvanuatuensis is virtually identical in size, color pattern, and degree of shell covered by pigment to N.macromphalus in New Caledonia, which is the Nautilus species geographically closest to Vanuatu. The new species we define here differs by always having an umbilical plug. Both species are ecologically similar in that mature specimens are commonly observed in very shallow water (up to 5 m depth) off Vanuatu and New Caledonia. As species show the similar, high degree of pigmentation, we assume that the shallow-water habitat visitation by both is the reason for their high level of pigmentation.
Etymology.
The specific epithet, an adjective, refers to the type locality, Vanuatu, where all the known specimens have been collected.
Habitat and distribution.
Nautilusvanuatuensis inhabits sites within Mele Bay, Vanuatu. Specimens were collected and filmed (Suppl. material 3: video 3) at depths of 200–400 m.
Conservation status
All nautiluses (family Nautilidae) are regulated under appendix II of the Convention on International Trade in Endangered Species (CITES). As of this writing, no species of Nautilus or Allonautilus has been formally assessed by the International Union for Conservation of Nature Red List.
Discussion
The populations of nautiluses within American Samoa, Fiji, and Vanuatu have already been effectively isolated from each other because of warm, surface seawater temperatures, depth implosion limits below 800 m, and their nektobenthic lifestyle, one of endless foraging just above the bottom, and thus within a few meters of the benthic environment at most. Here, we combined morphological characteristics with previously published population genomic results to newly describe each population of Nautilus within these archipelagos as a unique species. The characters that showed the most differentiation between the species included multiple color pattern traits (i.e., percent of shell pigmented in matures specimens and striping patterns) and, while not yet quantified, the actual “hue” of pigment in freshly caught specimens.
Fig. 7 shows the shell decoration and hood ornamentation of each of the species described here. Shell size at maturity also has discerning potential among some of the species’ groups (Fig. 8). Nautilussamoaensis sp. nov., N.vitiensis sp. nov., and N.vanuatuensis sp. nov. represent the easternmost range of extant nautilids and provide further validation for the decision to regulate all nautiluses (family Nautilidae) within appendix II of the Convention on International Trade in Endangered Species (CITES) given their morphological and genetic differences.
Shell diameter and shell pigmentation relationship of N.vitiensis sp. nov., N.samoaensis sp. nov., and N.vanuatuensis sp. nov. compared against each other as well as other Nautilus species and populations.
https://binary.pensoft.net/fig/800685
For comparative purposes, if we include the New Caledonian populations of nautiluses, N.macromphalus, with the three new species described here we can draw further inferences on the relationship of distinct species of nautiluses. The strongest morphologic similarity among the four species we designate as endemic to this region is between N.macromphalus and what the population assigned to N.pompilius from the Vanuatu archipelago, N.vanuatuensis sp. nov. They are clearly identified by the umbilical region, although indistinguishable in all other studied characters (Ward 1987). These two species are morphologically similar, as well as being geographically proximate to one another and, as noted above, also share the behavioral trait of commonly swimming at night into depths shallower than inhabited by any other Nautilus species. However, some of these traits must be adaptational, as these two species are not each other’s closest relatives (Fig. 2).
The third of the four species living in what we call an “South Pacific” biogeographic region (sensu Combosch et al. 2017), Nautilussamoaensis sp. nov. resembles both N.macromphalus and N.vanuatuensis sp. nov. in size and the relative amount of coloration on the shell but differ markedly in shell color “pattern.” It is sister to N.vitiensis sp. nov. and while these two species were ambiguously distinguished in prior genetic work, their reciprocal monophyly and the morphological differences outlined above, lead us to designate them as distinct species here.
Individuals of N.vitiensis sp. nov. in Fiji have never been seen at night, and the exceptionally low amount of pigmentation in this species may be due to an overall, deeper-water habitat, as discussed above. In any event, N.vitiensis sp. nov. has among the lowest degree of shell coloration of all currently defined species. New analyses of previously published shell formation temperatures of oxygen isotopes from shell and septal samples (Tajika et al. 2022) are consistent with the growth of juvenile species at depths below 300 m; these data, however, tell us nothing about habitation depths of the non-growing mature specimens.
Compared to N.macromphalus and N.vanuatuensis sp. nov., N.samoaensis sp. nov. has a unique species-level character: it has the most striking and readily identifiable ornamental pattern of any known Nautilus or Allonautilus species. Specimens captured with baited traps and observed through BRUVS observations made in 2013 at depths of 250–350 m all show coloration patterns on the middle portion of the phragmocone, which is the rare (for Nautilus), single character trait that identifies the species: a complex change in stripe direction (compared to striping found in any other Nautilus). Different as it is from the Vanuatu–New Caledonian species couplet, N.samoaensis sp. nov. still remains closer in observable shell characteristics to those two South Pacific species than it does to the geographically closer nautiluses of Fiji. The latter are smaller, and their shells bear a significantly different ornamentation than those of the other three species identified within this biogeographic region.
These data may be skewed, as all sampled populations of nautiluses report that males vastly outnumber females in traps, which is related to size at maturity. Nevertheless, the size at maturity remains a powerful character, and correlates well with genetic data. In fact, as we show here, the currently accepted and newly proposed species herein, with the sole exception of N.pompilius, can be statistically separated using a combination of the characters of mature shell size, percentage of shell covered by pigment, the morphology of the shell umbilical region, the morphology of the shell surface at a growth line scale, the thickness of the periostracum (which is dependent on shell surface morphology), and the morphology and color of the hood. Undoubtedly, other characters will be discovered when detailed dissection of the accepted species is finally attempted, including comparing the morphology of the radula and jaws. Nevertheless, even with the characters at hand, we show here that populations known to be separated by at least 200 km of deep water maintain significant genetic differences as well as measurable morphological differences, which is consistent with our conclusion that the populations of American Samoa, Fiji, and Vanuatu merit elevation to separate species. The use of morphological characters, shell pattern, and, to a lesser extent, shell size, have additional power when regulating and enforcing current trade regulations for all nautiluses. The fact that we were able to combine the morphology and genetics to differentiate these species provides a foundation for managers and other officials to begin to efficiently identify distinct species of nautilus shells that may come through as trade products.
Conclusions
The three species, N.vitiensis, N.samoaensis, and N.vanuatuensis represent populations of nautiluses on the easternmost edge of the overall habitat range of Nautilus. The designation of these three populations as distinct species provides insight into evolutionary radiation of the genus and clarification for future conservation practices.
Acknowledgements
We thank Michael Vecchione for assistance with curated specimens within the Smithsonian Institution. Associate Editor Jiří Frank, Amane Tajika, and an anonymous reviewer provided comments that helped refine this work. This manuscript was published by a grant from the Wetmore Colles Fund of the MCZ.
ReferencesBarordGJDooleyFDunstanAIlanoAKeisterKNNeumeisterHPreussTSchoepferSWardPD (2014) Comparative population assessments of Nautilus sp. in the Philippines, Australia, Fiji, and American Samoa using baited remote underwater video systems. PLoS ONE 9(6): e100799. https://doi.org/10.1371/journal.pone.0100799BonacumJLandmanNHMapesRHWhiteMMWhiteA-JIrlamJ (2011) Evolutionary radiation of present-day Nautilus and Allonautilus.29(1–2): 77–93. https://doi.org/10.4003/006.029.0221CarlsonBMcKibbenJDeGruyM (1984) Telemetric investigation of vertical migration of Nautilusbelauensis in Palau.38: 183–188.ComboschDJLemerSWardPDLandmanNHGiribetG (2017) Genomic signatures of evolution in Nautilus–An endangered living fossil.26(21): 5923–5938. https://doi.org/10.1111/mec.14344DunstanABradshawCJAMarshallJ (2011a) Nautilus at risk–Estimating population size and demography of Nautiluspompilius. PLoS ONE 6(2): e16716. https://doi.org/10.1371/journal.pone.0016716DunstanAWardPDMarshallNJ (2011b) Nautiluspompilius life history and demographics at the Osprey Reef Seamount, Coral Sea, Australia. PLoS ONE 6(2): e16312. https://doi.org/10.1371/journal.pone.0016312HabeTOkutaniT (1988) A new subspecies of living Nautilus (Cephalopoda: Nautiloidea) from the Sulu Sea.47: 91–94.HuangZHuangWLiuXHanZLiuGBoamahGAWangYYuFGanYXiaoQLuoXChenNLiuMYouWKeC (2022) Genomic insights into the adaptation and evolution of the nautilus, an ancient but evolving “living fossil.”.22(1): 15–27. https://doi.org/10.1111/1755-0998.13439JerebP (2005) Family Nautilidae. In: JerebPRoperCFE (Eds) Cephalopods of the World., 51–55.KrögerBVintherJFuchsD (2011) Cephalopod origin and evolution: A congruent picture emerging from fossils, development and molecules.33: 602–613. https://doi.org/10.1002/bies.201100001NikolaevaSSaundersWBMapsRAllcockAL (2015) Case 3703 Nautiluspompilius Linnaeus, 1758 (Mollusca, Cephalopoda, Nautilida): Proposed designation of a neotype.72(4): 274–285. https://doi.org/10.21805/bzn.v72i4.a21SaundersWB (1981) The species of Nautilus and their distribution.24: 8–17.SaundersWB (1984) The Role and Status of Nautilus in its Natural Habitat: Evidence from Deep- Water Remote Camera Photosequences.10(4): 469–486. https://doi.org/10.1017/S0094837300008472SaundersWB (1987) The species of Nautilus. In: SaundersWBLandmanNH (Eds) Nautilus: The Biology and Paleobiology of a Living Fossil., 35–52. https://doi.org/10.1007/978-1-4899-5040-6_3SaundersWB (1989) On the distribution of Nautiluspompilius in the Samoas, Fiji and Tonga.103(3): 99–104.SaundersWBDavisLE (1985) A preliminary report on Nautilus in Papua New Guinea.11: 60–69.SaundersWBLandmanNH (1987) Plenum Press, New York, 632 pp. https://doi.org/10.1007/978-1-4899-5040-6SaundersWBGreenfest-AllenEWardPD (2017) Demographic disequilibrium in living nautiloids (Nautilus and Allonautilus): Canary in the coal mines? PLoS ONE 12(7): e0179811. https://doi.org/10.1371/journal.pone.0179811SinclairBBriskeyLAspdenWPeggG (2007) Genetic diversity of isolated populations of Nautiluspompilius (Mollusca, Cephalopoda) in the Great Barrier Reef and Coral Sea.17(2–3): 223–235. https://doi.org/10.1007/s11160-006-9030-xSinclairWNewmanSJViannaGMSWilliamsSAspdenWJ (2011) Spatial subdivision and genetic diversity in populations on the east and west coasts of Australia: The multi-faceted case of Nautiluspompilius (Mollusca, Cephalopoda).19(1): 52–61. https://doi.org/10.1080/10641262.2010.533794ShigenoSAndrewsPLRPonteGFioritoG (2017) Cephalopod Brains: An Overview of Current Knowledge to Facilitate Comparison With Vertebrates. Frontiers in Physiology 9: e952. https://doi.org/10.3389/fphys.2018.00952TajikaAMorimotoNLandmanNH (2021) Significance of the suture line in cephalopod taxonomy revealed by 3D morphometrics in the modern nautilids Nautilus and Allonautilus. Scientific Reports 11(1): e17114. https://doi.org/10.1038/s41598-021-96611-1TajikaALandmanNHCochranJKGoiranCLe BouteillerA (2022) Isotopic evidence concerning the habitat of Nautilusmacromphalus in New Caledonia. PLoS ONE 17(7): e0271235. https://doi.org/10.1371/journal.pone.0271235VandepasLEDooleyFDBarordGJSwallaBJWardPD (2016) A revisited phylogeography of Nautiluspompilius.6(14): 4924–4935. https://doi.org/10.1002/ece3.2248WardP (1987) Allen and Unwin, Boston, 267 pp.WardPStoneRWestermannGMartinA (1977) Notes on animal weight, cameral fluids, swimming speed, and color polymorphism of the cephalopod Nautiluspompilius in the Fiji Islands.3(4): 377–388. https://doi.org/10.1017/S0094837300005534WardPCarlsonBWeeklyMBrumbaughB (1984) Remote telemetry of daily vertical and horizontal movement of Nautilus in Palau.309: 248–250. https://doi.org/10.1038/309248a0WardPDSaundersWB (1997) Allonautilus, a new genus of living nautiloid cephalopod and its bearing on the phylogeny of the Nautilida.71: 1054–1064. https://doi.org/10.1017/S0022336000036039WardPDooleyFBarordGJ (2016) Nautilus: Biology, systematics, and paleobiology as viewed from 2015.135(1): 169–185. https://doi.org/10.1007/s13358-016-0112-7WoodruffDSCarpenterMPSaundersWBWardPD (1987) Genetic variation and phylogeny in Nautilus.6: 65–83. https://doi.org/10.1007/978-1-4899-5040-6_5WoRMS Editorial Board (2021) World Register of Marine Species. https://www.marinespecies.org [Accessed 2022-01-03]WrayCGLandmanNHSaundersWBBonacumJ (1995) Genetic divergence and geographic diversification in Nautilus.21(2): 220–228. https://doi.org/10.1017/S009483730001321XZhangYMaoFMuHHuangMBaoYWangLWongN-KXiaoSDaiHXiangZMaMXiongYZhangZZhangLSongXWangFMuXLiJMaHZhangYZhengHSimakovOYuZ (2021) The genome of Nautiluspompilius illuminates eye evolution and biomineralization.5(7): 927–938. https://doi.org/10.1038/s41559-021-01448-6Supplementary materials10.3897/zookeys.1143.84427.suppl17575216F4D83F97-EFF2-507B-93B7-CF6E3E7C07F6
Supplemental video 1
video file
Baited remote underwater video systems (BRUVS) observations of Nautilusvitiensis sp. nov. recorded at approximately 300 m depth in Fiji.
https://binary.pensoft.net/file/800686This dataset is made available under the Open Database License (http://opendatacommons.org/licenses/odbl/1.0/). The Open Database License (ODbL) is a license agreement intended to allow users to freely share, modify, and use this Dataset while maintaining this same freedom for others, provided that the original source and author(s) are credited.Gregory J. Barord, David J. Combosch, Gonzalo Giribet, Neil Landman, Sarah Lemer, Job Veloso, Peter D. Ward10.3897/zookeys.1143.84427.suppl27575218332CC254-1986-5C3E-8984-CE1EACCB45D0
Supplemental video 2
video file
Baited remote underwater video systems (BRUVS) observations of Nautilussamoaensis sp. nov. recorded at approximately 300 m depth in American Samoa.
https://binary.pensoft.net/file/800687This dataset is made available under the Open Database License (http://opendatacommons.org/licenses/odbl/1.0/). The Open Database License (ODbL) is a license agreement intended to allow users to freely share, modify, and use this Dataset while maintaining this same freedom for others, provided that the original source and author(s) are credited.Gregory J. Barord, David J. Combosch, Gonzalo Giribet, Neil Landman, Sarah Lemer, Job Veloso, Peter D. Ward10.3897/zookeys.1143.84427.suppl37575224216EF3FC-1A98-593A-AAF8-4AC56F78C990
Supplemental video 3
video file
Baited remote underwater video systems (BRUVS) observations of Nautilusvanuatuensis sp. nov. recorded at approximately 300 m depth in Vanuatu.
https://binary.pensoft.net/file/800688This dataset is made available under the Open Database License (http://opendatacommons.org/licenses/odbl/1.0/). The Open Database License (ODbL) is a license agreement intended to allow users to freely share, modify, and use this Dataset while maintaining this same freedom for others, provided that the original source and author(s) are credited.Gregory J. Barord, David J. Combosch, Gonzalo Giribet, Neil Landman, Sarah Lemer, Job Veloso, Peter D. Ward