Bobtail squid are emerging models for host–microbe interactions, behavior, and development, yet their species diversity and distribution remain poorly characterized. Here, we combine mitochondrial and transcriptome sequences with morphological analysis to describe three species of bobtail squid (Sepiolidae: Sepiolinae) from the Ryukyu archipelago, and compare them with related taxa. One Ryukyuan type was previously unknown, and is described here as Euprymna brenneri sp. nov. Another Ryukyuan type is morphologically indistinguishable from Sepiola parva Sasaki, 1913. Molecular analyses, however, place this taxon within the genus Euprymna Steenstrup, 1887, and additional morphological investigation led to formal rediagnosis of Euprymna and reassignment of this species as Euprymna parva comb. nov. While no adults from the third Ryukyuan type were found, sequences from hatchlings suggest a close relationship with E. pardalota Reid, 2011, known from Australia and East Timor. The broadly sampled transcriptomes reported here provide a foundation for future phylogenetic and comparative studies.
Bobtail squid of the subfamily Sepiolinae Appellöf, 1898, including Euprymna Steenstrup, 1887 and Sepiola Leach, 1817, are small nektobenthic cephalopods generally found in shallow coastal waters of the Indo-west Pacific, the east Atlantic coast, and the Mediterranean Sea. The common name of these animals comes from their characteristic rounded (“bobbed”) posterior mantle. Bobtail squid lack a “true” sepion (cuttlebone) and the gladius (pen) is chitinous, reduced, or absent. Together with Idiosepiidae they are the sister group of the true squids (Teuthoidea)1.
Due to their small size and ease of culturing in captivity, species of Euprymna and Sepiola are increasingly emerging as model systems for a range of biological studies2,3,4. The Hawaiian bobtail squid Euprymna scolopes Berry, 1913 has become a prominent model for the study of symbiosis with their luminescent bacteria Vibrio fischeri located in the luminescent organ5,6. Associative learning, behavioral genetic studies, and the heritability of personality and fitness traits were also investigated in several species of bobtail squids7,8,9,10,11. The cultivation of E. scolopes, initially for studies of symbiosis, has promoted the detailed characterization of embryonic development, both morphologically12 and at the molecular level13,14,15. The small size of bobtail squid makes them ideal for advanced imaging16 opening up new opportunities for characterizing the cephalopod nervous system, complementing the extensive studies of the pygmy squid Idiosepius Steenstrup, 1881 by Shigeno and colleagues17,18,19. With the closure of the life cycle for several sepiolid squid20,21,22,23 (including Euprymna parva (Sasaki, 1913) comb. nov. described below), and the recently sequenced genome of E. scolopes24, these small cephalopods are emerging systems for comparative biology.
Over 68 species of Sepiolidae have been described25. Among the Sepiolinae, species of Euprymna can be distinguished by the absence of a distinct copulatory apparatus in their hectocotylus, the modified left arm 1 in males involved in mating, and the number and organization of arm sucker rows. Within Euprymna, in addition to the differences in the hectocotylus among species, the nature and arrangement of male enlarged arm suckers are among the key characters used to distinguish species. Unfortunately, the suckers readily become dislodged from preserved specimens during examination, often confounding definitive taxonomic identification. As in all Sepiolinae, most distinguishing morphological characters are found only in males, making it very difficult to identify females using morphology alone. The potential for phenotypic plasticity as described in males of Sepiola birostrata Sasaki, 191826 and the shortage of distinguishing morphological characters for species of the Indo-Pacific Euprymna and Sepiola are also problematic.
More than a century of classical morphology-based taxonomy has more recently been augmented by surveys of the mitochondrial cytochrome oxidase I (COI) marker in bobtail squids27,28,29,30,31,32,33,34,35,36, especially in the subfamily Sepiolinae. While COI molecular characters (i.e., variable sites) supplement morphological features in this taxonomically tricky group of cephalopods, several misidentifications have been reported for the North Sea Sepiola species after COI sequencing and morphological analysis37. Transcriptome sequences complement DNA barcoding and morphological analysis by providing sequence data from multiple unlinked nuclear coding regions. Information from these loci enables more accurate species identification and the reconstruction of their phylogenetic relationships.
Here, we characterize bobtail squid from the Okinawa and Yaeyama islands of the Ryukyu archipelago, a region known for its rich marine diversity38. Our aim is to describe the sepiolines of the Ryukyus and set them within the broader systematic framework of Indo-Pacific bobtail squid. We found three different species of bobtail squid in these waters, and characterized them using COI sequences, transcriptome sequences, and morphology. One Ryukyuan species, recognized by the molecular traits of laboratory hatchlings, appears to be closely related to Euprymna pardalota Reid 2011 described from northern Australia. A second species is indistinguishable from Sepiola parva Sasaki 1913, but comparative molecular analysis and reexamination of morphology indicates that this taxon should instead be assigned to the genus Euprymna, which we also revise. The third Ryukyuan species is morphologically and molecularly distinct from other sepiolines. We formally describe this new species here and name it in honor of Sydney Brenner, pioneering molecular geneticist and supporter of Okinawan science.
This study is the most comprehensive COI analysis of the Sepiolidae published to date. The optic lobe transcriptome sequences reported here will prove valuable for resolving the phylogenetic relationships among this increasingly studied group of cephalopods.
We found eggs of three distinct sizes and/or clutch morphologies while collecting around the Ryukyu islands (Fig. 1a), and designated them Types 1–3 (Fig. 1b) (see Materials and methods). We consistently obtained hatchlings for all three egg types in laboratory aquaria (Table 1, Methods), enabling genetic analysis and sequence comparison with adults. We found only two distinct adult types (Fig. 1c) and associated these adult forms with Types 2 and 3 hatchlings using mitochondrial COI sequences (Fig. 2). Types 2 and 3 hatchlings could be raised to reproductively mature adults in the laboratory (Methods), further corroborating their match with the two adult types found in the wild. During our samplings from February to November over several years (Methods) we did not find any Type 1 adults, and Type 1 hatchlings were recalcitrant to culture.
To examine relationships among the Ryukyuan types and other species, we used maximum likelihood to estimate a phylogenetic tree with haplotypes from COI sequences (Fig. 2), combining publicly deposited data (Supplementary Table 1) with 41 additional sequences from our Ryukyuan samples and 42 new sequences from 9 previously described bobtail and related squid species (Materials and methods; Supplementary Table 2). We found that Ryukyuan Type 1 formed a clade with, and is clearly related to, E. pardalota, a species described from northern Australia39. Ryukyuan Type 2 lies within a clade identified as Sepiola parva Sasaki, 1913 from Sagami Bay in mainland Japan, near the type locality for this species. The Sepiola parva clade (including the Ryukyuan Type 2), however, lies within the Euprymna clade, and appears to render the genus Euprymna as polyphyletic. We confirm this placement below with both transcriptome data and morphological analysis, and propose a revised assignment of Sepiola parva to the genus Euprymna. The COI sequence for Ryukyuan Type 3 did not match any of the sequences deposited in Genbank to date.
To avoid dependence on a single mitochondrial marker, for additional phylogenetic resolution, and to capture the nuclear variation within and between species, we also systematically sampled transcriptomes of hatchling and/or adult Ryukyuan bobtail squid types along with 17 individuals identified from six known Indo-Pacific sepiolines (Materials and methods; Supplementary Data). RNA from optic lobe was preferred because this organ is easily and reproducibly dissected, and provides deep coverage of genes associated with neural and other functions, although mantle tissue was also used for some individuals. While we were unable to obtain samples of Euprymna hyllebergi, reportedly found in the Gulf of Thailand, the Andaman Sea23,40 and the South China Sea41, this species is clearly distinct from our Ryukyuan types based on COI analyses (Fig. 2) and morphology. For outgroups, we added transcriptome data from the tropical bottletail squid Sepiadarium kochii Steenstrup, 1881, and the pyjama squid Sepioloidea lineolata (Quoy & Gaimard, 1832), both members of the family Sepiadariidae, which appears to be the sister taxon to the Sepiolidae42,43,44.
Both maximum likelihood and Bayesian phylogenetic analyses obtained from 452 orthologous bobtail squid genes show that our three Ryukyuan types form three well-separated clades, consistent with their distinct egg mass types, mitochondrial COI, and (for Types 2 and 3) adult morphology (Fig. 3).
Classification of Ryukyuan species
Ryukuan Type 1 is clearly distinct from other nominal Indo-Pacific bobtail squid (Euprymna berryi Sasaki, 1929, Euprymna morsei, E. scolopes, Euprymna tasmanica (Pfeffer, 1884), S. birostrata), and represents a distinct species. Since we did not find wild adults whose COI sequence matched Type 1 eggs and could not raise hatchlings to adults (Methods), however, we could not assert Type 1 as a new species because formal identification of bobtail squid is based on adult morphology. Type 1 hatchlings have a bilobed light organ, a broad ligament between head and mantle, and two rows of arm suckers (as in E. pardalota, Euprymna phenax, and E. parva (formerly S. parva, see below)), consistent with assignment to the genus Euprymna. It would be interesting to determine whether the club suckers of Type 1 have the distinctive finger-like papillae as noted for E. pardalota Reid39: Fig. 4d) and S. parva (Takayama and Okutani26: Fig. 6). Although based on the COI marker Type 1 appears to be most closely related to E. pardalota (from Australia and East Timor), the COI distance exceeds typical intra-specific variation37,45 (Supplementary Note 2). Unfortunately no RNA samples were available from this species, so we could not apply the more sensitive transcriptome analysis.
Ryukyuan Type 2 forms a clade with Sepiola parva from mainland Japan based on transcriptome analysis, COI marker, and morphology. Type 2 squid therefore conform in all respects to the species originally described, and recognized in the published literature, as Sepiola parva Sasaki 1913. We confirmed this (in the absence of the type specimen) by collecting additional specimens from Sagami Bay, close to the type locality (Methods). The identification of Ryukyuan Type 2 with S. parva Sasaki 1913 from Sagami Bay (redescribed below as E. parva comb. nov.) is consistent with dispersal of the species along the Kuroshio current that connects Zamami Island and western Okinawa in the south with Sagami Bay in the north.
Phylogenetic analysis based on both transcriptomes and COI, however, shows that type 2/S. parva is nested within the Euprymna clade. Thus the assignment of this species to the genus Sepiola renders the genus Euprymna polyphyletic. In our transcriptome analysis S. birostrata appears as the sister group to the Euprymna species, including all three Ryukyuan types. We conclude that Type 2/S. parva belongs in the genus Euprymna rather than Sepiola, based on molecular as well as morphological characters. We, therefore, propose a new generic combination, Euprymna parva comb. nov., for this taxon (see Systematic Descriptions). Our findings also required revision of the diagnosis for Euprymna (see Systematic Descriptions).
Ryukyuan Type 3 is distinct from all other bobtail squid based on both molecular (COI and transcriptome) and morphological characters. We propose below that Type 3 represents a novel species of Euprymna, described formally below (Systematic Descriptions).
Molecular and temporal divergence
Pairwise synonymous substitution rates (Ks) between clades are shown in Supplementary Fig. 1. The genetic distances (Ks) within each Ryukyuan type are small compared with the distances between them. The divergence among Euprymna species, including Type 1, Type 2 /“S”. parva, and Type 3, is considerable (5.1–18.6%), but not as great as the divergence between S. birostrata and Euprymna species (except Ryukyuan Type 1 and Type 2/“S”. parva) which is notably higher (33.8–38.4%), consistent with the assignment of these taxa to distinct genera. The divergence between Type 1, Type 2/“S”. parva and S. birostrata is also high (32.6–40.5%) and is comparable to the intergeneric divergence between S. birostrata and Euprymna spp. (including Type 3).
Using a local molecular clock method and calibrations from Tanner et al.1, we estimate that the Indo-Pacific Euprymna, including Ryukyuan Types 1–3, diverged from each other 15–25 Mya (Methods). If the molecular clock is accurate, then these lineages diverged prior to the partial submergence of the Miocene land-bridge that connected eastern China to the main island of Japan ~10 Mya46.
Here, we present formal descriptions of (1) the genus Euprymna Steenstrup, 1887; (2) Euprymna parva comb. nov., formerly Sepiola parva; and (3) the new Euprymna species.
Euprymna Steenstrup, 1887
Gender feminine. Type species, by subsequent designation, Inioteuthis morsei Verrill, 1881. Recent. Western Pacific and eastern Indian Oceans.
(Amended from Norman and Lu47 and Reid39, and after Bello, personal communication.) Broad ligament between head and mantle; commissure greater than one-third of head width. Transverse suckers in two or more rows on normal (non-hectocotylised) arms. Stalked suckers in six or more transverse rows on tentacular clubs. Left arm 1 hectocotylised in mature males; distally with lengthened, columnar sucker pedicels, closely packed to form longitudinal “palisades”, bearing at tip embedded toothed suckers that are partially covered by fleshy cap, number of palisades proximally equal to that of regular sucker rows but reduced toward distal tip of arm; pedicels not bearing discretely demarcated rounded suckers; basal part of hectocotylised arm with normal suckers and sometimes with 1–2 finger-like papillae in ventral sucker row, sometimes bearing tiny sucker(s). Enlarged arm suckers usually present in male and sometimes present in females. Paired kidney-shaped light organs in mantle cavity, ventral, and closely adherent to ink sac. Gladius absent.
Given that some Euprymna are now known to have biserial arm suckers, members of the genus Sepiola seem superficially to conform to this diagnosis. However, these two taxa (i.e., Euprymna and Sepiola) clearly differ based on molecular traits and in a number of other important characters in detail. The modification of the hectocotylus is quite distinct. In Sepiola, the hectocotylised left dorsal arm is thicker than the right and strongly recurved aborally in preserved specimens. The palisade columnar suckers in the hectocotylus distal portion are unique for Euprymna. Sepiola as well as all the other Sepiolinae genera bear regular suckers in the distal part of the hectocotylus. Some of them may be enlarged in some species, their stalks may be also lengthened and/or swollen, but no other Sepiolinae species have columnar stalks with embedded suckers at their tips. Although the suckers are positioned on enlarged and elongate pedicels in both taxa, the suckers are ovoid and discrete in Sepiola, while in Euprymna the suckers are partially capped or encased by the pedicels and the chitinous rims are usually narrow. Most remarkably, in Sepiola, instead of a finger-like papilla at the base of the hectocotylus (as seen in most Euprymna species) there is a distinct fleshy mound that may bear hook-like projections. The third arms of Sepiola males are thick and strongly curved orally in some species; in Euprymna the third arm pair of males is not swollen and recurved. Sepiola generally have two rows of suckers on each arm (as do some species of Euprymna), but some species have 4–8 rows of suckers on the distal tips of the fourth (ventralmost) arm pair. Euprymna may have two or more rows of arm suckers but if four or more rows are present, they are not confined to a single arm tip. In addition, the tentacular club is recurved and relatively short in Euprymna and longer and much less curved in Sepiola with a much narrower keel. The fins in Sepiola are large and round, while in Euprymna the fins are narrower and more elongate in outline.
Euprymna parva (Sasaki, 1913), comb. nov.
Sepiola parva Sasaki, 1913: 252, Fig. 4. — Sasaki, 1929: 136–137 Pl. XV, Figs. 4 and 5, text Fig. 80; Takayama and Okutani, 1992: 203–214, fig, 2, Figs. 4–6. — Okutani, 1995: 45, fig. 43. Reid and Norman, 1998: 717. — Reid and Jereb, 2005: 165–166, fig. 239.
Inioteuthis parva Sasaki, 1914: 595, pl. 11 Figs. 9 and 10.
Type locality: Japan, Tokyo Bay.
3♂ (8.5–10.7 mm ML), 3♀ (7.0–8.0 mm ML), East China Sea, Okinawa, Diamond Beach in Seragaki, 26.51N, 127.88E, <2 m, 15 June 2016, coll. J. Jolly, G. Sanchez, A. Masunaga & K. Asada (AM C.574777, Hap 3, and GenBank accession number: LC417215).
The correct generic placement of this taxon has been equivocal since it was first described. It was first placed in Sepiola, transferred to Inioteuthis Sasaki, 1914, then later retained in the genus Sepiola. Sasaki does not explain why parva was placed in Sepiola in his 1929 treatise, nor why it was referred to Inioteuthis in his 1914 work. Clearly, however, the features noted by Sasaki, “the nipple-like protruberance” near the base of the hectocotylus and the “peculiar and unstalked cylindrical suckers” (Sasaki48: 137) are characteristic of Euprymna. Mature males have two rows of suckers on their arms, in contrast to the four rows typically (but not always) found among Euprymna. This has, no doubt, resulted in its misplacement in the genus Sepiola, that has continued largely without question until now. However, two rows of arm suckers are also found in E. pardalota and E. phenax. The inclusion of the E. pardalota COI sequence in our analyses (Fig. 2) confirms its position, and that of “Sepiola” parva in the monophyletic genus Euprymna. Optic lobe transcriptome data (Fig. 3) clearly places S. parva in the monophyletic Euprymna clade, and the pairwise synonymous substitution rate (Ks) between clades (Supplementary Fig. 1) highlights the disjunction between Euprymna and Sepiola, providing strong support for their distinct generic status. The genetic distance data fully supports the placement of S. parva in the genus Euprymna and this evidence now permits a more robust definition of the genus based on morphological characters.
The hectocotylus (dorsal left arm) of Euprymna is unique among the Sepiolinae. In all genera but Euprymna, the hectocotylus is clearly tripartite, with a morphologically distinct basal part, copulatory apparatus, and distal part49,50. In contrast, in Euprymna, the hectocotylized arm has a bipartite form, with a proximal portion and a distal modified part. In Euprymna there is no distinct copulatory apparatus, instead the pedicels of the ventral suckers in the third to fourth proximal rows are modified to form 1–2 papillae in most species, sometimes bearing a vestigial sucker, whereas in all other genera the sucker pedicels forming the copulatory apparatus are more conspicuously modified (mostly horn- or hook-like). More importantly, the distal-most portion of the Euprymna hectocotylus bears deeply modified sucker-stalk elements: the stalks are columnar, i.e., thickened and lengthened, and appressed to each other to form palisades, and the sucker proper is reduced to a small opening surrounded by a chitinous rim, often covered by a fleshy cap and embedded in the columnar pedicel. On the contrary, in all other genera, the hectocotylus distal suckers are normal (in some cases some of them may be enlarged and/or their stalks slightly lengthened) (Bello, submitted). The very simple copulatory apparatus of Euprymna is considered a plesiomorphic character state51 in the Sepiolinae, placing this genus in a basal position within the subfamily36,52.
Euprymna brenneri sp. nov.
HOLOTYPE 1♂, 14.9 mm ML, immature, Okinawa, Diamond Beach in Seragaki, 26.51N, 127.88E, 26 Apr. 2016, coll. J. Jolly & O. Simakov (NSMT Mo 85885). PARATYPES Okinawa, Seragaki, Diamond Beach, 26.51N, 127.88E, 26 Apr. 2016, coll. J. Jolly & O. Simakov: 1♂, 18.8 mm ML, (NSMT Mo 85886); 1♂, 9.0 mm ML, immature (NSMT Mo 85887); 1♂, 10.6 mm ML, immature (NSMT Mo 85888); 1♀, 19.5 mm ML, immature (NSMT Mo 85889); 1♀ 11.6 mm ML, immature (NSMT Mo 85890). Okinawa, Miyagi Is, 26.38N, 127.99E, <2 m: 1♂, 22.0 mm ML, mature, 18 Mar. 2016, coll. B. Grasse, J. Jolly, O. Simakov, S. Nyholm, K. Keunig, A. Masunaga, F. Marletaz (NSMT Mo 85891, Hap 23, and GenBank accession number: LC417234); 1♀, 9.1 mm ML, immature, 24 Feb. 2018, coll. G. Sanchez, J. Jolly, C. Sugimoto, K. Asada (NSMT Mo 85892, Hap 12, and GenBank accession number: LC417223). Okinawa, Kume Is, 23.33N, 126.81E, 1♀, 15.3 mm ML, immature, 12 Nov. 2018, coll. R. Minemizu (NSMT Mo 85893).
Notes: Only one male was reproductively mature, but due to damage to the arms and missing suckers this specimen was not selected as the holotype. No females were reproductively mature. All specimens with the exception of NMST Mo 85891 and NMST Mo 85892 were laboratory-reared from collected eggs.
Other material examined
Syntypes: Euprymna bursa, Hong Kong, ♀ (34.4 mm ML), ZMH 1393, ZMH 1384 ♀ (~25 mm ML).
Small species, largest examined specimen (male, mature) 22.0 mm mantle length. Arm suckers biserial proximally and at distal tips, rest tetraserial. Males with enlarged suckers in dorsal and ventral rows of arms 3 and 4 (from ~5th to 8th sucker row from base on arms 3 and from ~7th to 9th sucker row from the base of arms 4). Hectocotylus without finger-like papillae basally. Females with enlarged suckers in ventral row of arms 3 (from ~8th to 13th sucker row from the arm base) and dorsal and ventral row of arms 4 (from ~10th sucker row counting from the basal-most row of suckers). Male enlarged suckers relatively larger than female arm suckers; suckers on ventral side of arm 3 larger than remaining enlarged suckers in both sexes. Enlarged suckers not in continuous rows, but interspersed with small suckers.
Counts and indices for individual specimens are given in Supplementary Table 3.
Species relatively small: ML males examined 8.6–22.0 mm ML, females 8.5–19.5 mm ML. Mantle short, broad, dome-shaped posteriorly (Fig. 4a, b); MWI males 63.6–98.8, females 62.1–94.1. Dorsal mantle joined to head by broad commissure, ventral mantle margin wide “m” shape (Fig. 4b). Fins oval; length approximately 50% ML; FIIa males 26.4–31.9, females 25.6–32.9; fin width about 30% ML, FWI males 23.9–34.9, females 21.6–45.8, attached dorso-laterally midway along mantle. Fins do not project anteriorly as far as anterior mantle margin (Fig. 4a, b).
Funnel conical, projects anteriorly beyond ventral mantle margin (Fig. 4b). FuLI males 52.3–75.5, females 52.3–67.2; free for most of its length, FFuI males 27.3–47.2, females 33.3–41.2. Funnel-locking cartilage long, narrow, parallel-sided with shallow groove of uniform depth and thickened rim. Mantle cartilage a long straight ridge (Fig. 5a). Funnel valve a tiny flap. Funnel organ (Fig. 5b) dorsal element broad, inverted V-shape, with concentration of glandular tissue mid-anteriorly; ventral elements with acute anterior tips.
Head broader than long, HLI males 47.0–69.8, females 51.7–65.4; HWI males 66.0–96.5, females 62.6–91.8. Eyes large, EDI males 11.6–23.6, females 14.4–20.7; ventral eyelids free. Distinct, large photosensitive vesicle on latero-posterior surface of head, posterior and ventral to eyes.
Arms, broad basally, tapered distally; order 3 > 1 > 2 = 4 or 3 > 2 > 1 = 4 (Supplementary Table 3). Arm length index of longest arm in males (ALI3) 97.3, female (ALI3) 92.3; arm keels absent or indistinct. All arms connected by relatively shallow webs, protective membranes absent. Arm sucker pedicels without lappets. Arm suckers tetraserial, with some biserial suckers at base and at distal tips of arms; spherical on normal arms (Fig. 5c, d) (hectocotylus differs). Chitinous sucker rims: infundibulum with 3–4 rows of pavement-like processes (Fig. 5e, f), peripheral sucker rim processes wedge-shaped, rest irregular with slightly raised outer margins (Fig. 5f). Chitinous inner rim of normal arm suckers without teeth, slightly crenulated on one side (Fig. 5f). Suckers on modified region of hectocotylus with toothed margins (Figs. 6 and 5a).
Males (Fig. 5c) and females (Fig. 5d) with enlarged suckers on outer row(s) of arms 3 and 4. Enlarged suckers clearly discernible in both sexes, even those of the smallest sizes (male 8.6 mm ML, female 8.5 mm ML). Male enlarged suckers larger than female arm suckers (Supplementary Table 3). Sucker counts range from 60 to 112 on each arm; Arms 2 with a greater number of suckers than other arms in both sexes.
Males with arm suckers in the following variable arrangement from proximal to distal end of arm:
Right Arms 1 and Arms 2: 5 rows biserial suckers, rest tetraserial. None enlarged.
Arms 3: 5 rows biserial suckers, rest tetraserial, distal arm tip with ~6 rows biserial suckers. Dorsal rows distal to sucker rows ~5–7 with 4–9 enlarged suckers interspersed at intervals with regular-sized suckers. (Larger specimens with greater number of enlarged arm suckers.) Ventral rows with ~5 enlarged suckers interspersed at intervals with regular-sized suckers.
Arms 4: (Fig. 5c) 5 rows biserial suckers, rest tetraserial, distal tip of arm with ~3 rows biserial suckers. Dorsal rows distal to sucker rows ~7–9 with ~3–4 enlarged suckers interspersed at intervals with regular-sized suckers. Ventral rows after sucker rows ~7–9 with ~2–7 enlarged suckers, some alternating at intervals with regular-sized suckers.
Females with enlarged arm suckers in the following variable arrangement from proximal to distal end of arm:
Arms 1: 4–5 rows biserial suckers, rest tetraserial, distal 4 rows biserial. None enlarged.
Arms 2: 2–4 rows biserial suckers, rest tetraserial, distal 6 rows biserial. None enlarged.
Arms 3: 5 rows biserial suckers, rest tetraserial, distal tip of arm with ~8–10 rows biserial suckers. Dorsal rows without enlarged suckers. Ventral rows with ~8–13 rows of normal suckers proximally followed by ~4–5 enlarged suckers alternating at intervals (either large and small suckers alternate, or two large suckers alternate with 1–2 regular-sized suckers) toward distal half of arms.
Arms 4: ~8–9 rows biserial suckers, rest tetraserial, distal tip of arm with 4–5 rows biserial suckers. Dorsal rows with enlarged suckers in rows ~11–15. Ventral rows with enlarged suckers in rows ~10–14.
In both sexes the enlarged suckers on arms 3 are larger than those on arms 4 and those in the ventrolateral rows are larger than those on the dorsolateral rows. The enlarged suckers on arms 3 displace the regular-sized suckers laterally. (The arrangement of enlarged suckers varies considerably among the specimens examined and it would be useful when more material becomes available to map the arrangement of enlarged suckers in mature specimens of both sexes and over a range of specimen sizes to determine whether a clear pattern of regular and enlarged suckers can be discerned.).
Left dorsal arm of males hectocotylised: from base to distal end of arm, one single sucker, ~seven transverse rows of normal tetraserial suckers, remaining suckers with swollen pedicels, that form palisade arrangement (Fig. 6), biserial with integument partially covering chitinous sucker rim in cap-like arrangement. No finger-like papillae at base of hectocotylised arm. Right dorsal arm of males with transverse rows of “normal” tetraserial suckers, with swollen pedicels.
Tentacles slender, stalks naked, semicircular in section. Club relatively short; ClLI males 18.6–33.0, females 17.9–32.9, recurved in preserved specimens, tapers to blunt end distally; sucker-bearing face convex. Suckers ~0.04–~0.08 mm diameter in center of club; arranged in ~16–24 crowded oblique rows (Fig. 7b). Swimming keel on aboral side of carpus broad, extends posteriorly well beyond carpus. Club sucker dentition (Fig. 7c, d): inner ring without teeth; infundibulum with three rows of pavement-like processes; inner rows sub-rectangular, narrowing toward central opening; middle and outer rows ovoid; irregular, with strongly crenulated and pitted surface.
Well-developed light organ present overlying and associated with ink sac (Fig. 7e). Individual lobes rectangular bulb-like anteriorly, slightly enlarged; rounded posteriorly.
Gills with 24–27 lamellae per demibranch. Buccal membrane with six lappets; suckers absent.
Radula with seven transverse rows of teeth (Fig. 7f). Rhachidian teeth simple, without cusps, triangular, slightly concave laterally and ventrally. First lateral teeth similar in size and shape to rhachidian teeth with pointed cusps displaced laterally and directed toward midline of radula. Second and third laterals with elongate bases, longer, curved. Third laterals with scythe-like teeth, longer than second laterals.
Upper beak (Fig. 7g) with pointed rostrum, hood curved, high above crest posteriorly; jaw angle approximately 90°; lateral wall edge with slight indentation. Lower beak (Fig. 7h) with blunt protruding rostrum, rostral edge obtuse, curved, without distinct inner angle; hood notch absent, wings almost straight. Distinct dark pigmentation restricted to rostrum and hood of upper and lower beaks.
Spermatophores (fully developed only in NSMT Mo 85891) approximately ½ mantle length. Sperm reservoir contains coiled sperm cord (Fig. 8a). Cement body unipartite; cylindrical, approximately uniform width, connects to sperm reservoir via a broad duct (Fig. 8a, b). Oral end of ejaculatory apparatus with 3–4 simple coils. Male reproductive tract similar in structure to congeners (Fig. 8c). Spermatophoric gland with very large, bulbous terminal portion.
Female reproductive tract: Ovary occupies large proportion of posterior end of mantle cavity and opens via single thick-walled oviduct at anterior end on left side. Nidamental glands paired, broad, located ventral to ovary toward anterior end. Inverted brownish-colored U-shaped accessory nidamental glands located toward distal end of nidamental glands. Large sac-like bursa copulatrix on animals’ left side. Spawned eggs 4 mm diameter with jelly coat and sand, 3 mm without jelly coat. Eggs are laid in clusters of more than 100, rather than individually (Fig. 1b, Type 3). Hatchlings 2 mm ML (Fig. 9a–c, Table 1).
Alcohol preserved specimens cream to maroon with large deep purple spots on dorsal and ventral head and mantle; spots larger and animal darker on dorsal surface (Fig. 4a, b); few scattered chromatophores on arms. Shiny bluish iridophores on head around eyes. Fins with large spots dorsally, close to junction with mantle, otherwise chromatophores absent from fins dorsally and ventrally. Club without pigment spots. Live adults rust brown with evenly scattered, relatively small pigment spots, darkest dorsally (Fig. 1c Type 3; Fig. 9d, e). Bright bluish iridophores around eyes, along anterio-dorsal rim of mantle, and underlie pigment spots on dorsal mantle (Fig. 9e). Arms banded with regular large spots and bars along their length (Fig. 9d) that can be seen even in embryos inside the eggs (Fig. 9a). Hatchlings translucent with evenly scattered chromatophores. Juveniles dark brown.
Adults were found in sandy near-shore shallow waters, less than 2 m in depth, among corals and rocks. Eggs were found in rocky areas near coral reefs in depths of 8–18 meters.
Japan, Okinawa, Seragaki, Diamond Beach, 26.51N, 127.88E.
Japan: Okinawa Prefecture Seragaki, Diamond Beach 26.51N, 127.88E; Oura Bay, 26.53N, 127.74E; Miyagi Island, 26.38N, 127.99E; Ishigaki Island, Oganzaki 24.44N, 124.07E; and Kume Island, Northern Hatenohama Beach (26.35°N, 126.86°E) (Fig. 1). Taiwan*: off Penghu waters on the west-northern side of Sha-kang Fishing Harbor 23.60N, 119.62E. Depth range 2–18 m. (*Based on COI obtained from a single immature specimen.)
The species is named in honor of the pioneering geneticist and Nobel Laureate Dr Sydney Brenner, founding president of the Okinawa Institute of Science and Technology. We also propose the common name Brenner’s bobtail in English and Burenā-mimika in Japanese.
The largest male (22 mm ML) (and the only fully mature specimen) examined had damaged arm tips and most suckers missing. However, the arrangement of enlarged suckers was clear from the sub-mature specimens.
Prior to this study fifteen species of Euprymna were recognized25, although three of these (E. bursa Pfeffer, 1884, E. pusilla Pfeffer, 1884 and E. schneehagenii Pfeffer, 1884) are considered doubtful species by Norman and Lu47. Among the nominal species of Euprymna, the species whose geographic range most closely encompasses the known range of E. brenneri includes E. berryi, which has been found in warm temperate coastal waters from China and Taiwan, south to Hong Kong and Japan53, and E. morsei, which is sympatric with E. berryi over its range and also occurs as far south as the Philippines and Indonesia. Both, however, differ in morphology and in molecular traits (Figs. 2 and 3) from Euprymna brenneri. These three taxa (E. berryi, E. morsei and E. brenneri) differ in their COI and transcriptome signatures. Both E. berryi and E. morsei have enlarged suckers in males on the second arm pair (on the ventral margin in E. morsei and the dorsal and ventral margins in E. berryi), while E. brenneri does not. Kubodera and Okutani32 described E. megaspadicea, found in deep waters (200 m) of Nago Bay off Okinawa. While no sequence data currently exists for E. megaspadicea, it is clearly morphologically distinct from E. brenneri. In E. megaspadicea the hectocotylised arm is longer than the opposing arm, and the hectocotylus contains a sharp lateral inward groove not seen in other Euprymna species.
As part of this study we examined the type specimens of E. bursa (ZMH RK 1384 and RK 1393, both females, approximately 25 mm ML and 34 mm ML respectively) from Hong Kong. Eurymna bursa differs from E. brenneri in that none of the arm suckers are enlarged (luckily these remain attached to the arms of the E. bursa types, enabling this comparison to be made). In addition, E. bursa has a greater number of arm suckers (102–128) and the median component of the funnel organ of E. bursa is spade-shaped, straight posteriorly, and not indented. (Whether E. bursa is a valid species awaits the examination of males from the type locality; here we verified that E. brenneri was not referable to this species—particularly important given their geographical proximity.)
Of the remaining Euprymna species (which now also includes E. parva), the results of the COI analyses (Fig. 2) indicate that E. brenneri (i.e., Ryukyu Type 3) belongs in a clade distinct from E. berryi; E. hyllebergi; E. morsei; E. pardalota; E. scolopes, E. tasmanica, E. albatrossae Voss 1963, and Euprymna sp. Type 1. Transcriptomes separate E. brenneri from E. berryi, E. morsei, E. parva, E. scolopes, and E. tasmanica and Euprymna sp. Type 1 (Fig. 3). These differences are also supported by morphological traits: no other Euprymna taxa are yet known to include females with enlarged suckers. In addition, male E. albatrossae; E. berryi, E. megaspadicea, E. morsei, E. scolopes, E. stenodactyla Grant, 1833, and E. tasmanica have enlarged suckers on the second arm pair of males, which is not the case for E. brenneri.
Euprymna brenneri does, however, have enlarged suckers on arms 3 and 4. Males and females have enlarged suckers on the ventral row of the third arm and the dorsal and ventral rows of the fourth arms, with no enlarged suckers on the first and second arms. This is the first time a female Euprymna has been identified with large suckers. Female members of this genus are notoriously difficult to identify based on morphology, so the discovery of this character is a valuable one. Of the other nominal species, the enlarged sucker arrangement in male E. brenneri is most similar to that of E. hoylei Adam, 1986, but this species (in addition to all other nominal Euprymna with the exception of E. brenneri) have 1–3 enlarged finger-like papillae on the proximal end of the hectocotylised arm. Euprymna hoylei, described from the Sulu Archipelago, like E. brenneri, has no enlarged suckers on the second arm, however, E. brenneri males possesses approximately eight very large suckers on the third arm compared to a smaller number described for E. hoylei (3–4). Female E. hoylei do not have enlarged suckers. In addition to the presence or absence of enlarged suckers on particular arms, the enlarged suckers in both sexes of E. brenneri are not located close to the base of the arms, as seems to be the case in other Euprymna species, but at some distance distal to the arm bases.
Here we report three distinct species of bobtail squid living in the waters of the Ryukyu islands, based on differences in egg mass, morphology, mitochondrial COI and transcriptome-based molecular markers. Moreover, we identify a novel bobtail squid species, E. brenneri; document that the species known as Sepiola parva should in fact be classified within the genus Euprymna, Steenstrup 1887, and close its life cycle in laboratory culture; provide an updated definition of the genus Euprymna and E. parva comb. nov.; update the DNA barcoding data set of bobtail squid; and provide a set of useful genes from the optic lobe of bobtail squid for future comparative and phylogenetic studies.
Broader perspectives on Sepiolid phylogeny
Our analysis of diverse bobtail squid supports the monophyly of the genus Euprymna and the genus has been redefined based on morphological characters (Systematic Description). We find that four rows of arm suckers is, however, not a defining character for the clade, and the group includes at least four members with two rows of arm suckers: Euprymna sp. Type 1, E. pardalota, E. parva, and E. phenax. This undoubtedly resulted in the original misplacement of E. parva in the genus Sepiola. Evidently the two-row state is ancestral for Euprymna, and is retained in E. parva and Euprymna sp. Type 1 (observed in hatchlings). The four rows found in most of the remaining Euprymna (E. stenodactyla has 6–8), including E. brenneri and other Euprymna spp. in Fig. 3, is a derived state.
The genus Sepiola originally described by Leach54 united Atlantic and Mediterranean species of bobtail squid. It was later extended by Sasaki55 to include the Indo-Pacific species, Sepiola parva, S. birostrata and later, S. trirostrata Voss, 1962. In our analysis (and in Lindgren et al.42, Allcock et al.56, and Lindgren et al.57) with fewer species but more molecular characters, this extended version of the genus Sepiola sensu Sasaki appears to be polyphyletic. Also, in our COI tree (Fig. 2) Sepiola birostrata from Japan is only distantly related to the Sepiola species from the Mediterranean, and the North and Baltic Seas. This latter group is, in turn, interspersed among species of the genus Sepietta and Heteroteuthis. A critical reexamination of these relationships is needed.
The complex modification of the basal part of the hectocotylus characteristic of Sepiola (and indeed other members of the subfamily), albeit in different degrees, appears to be an ancestral character of a broader clade that includes the Atlantic-Mediterranean Sepiola. The genus Euprymna evidently arose from within this broader clade, accompanied by a simplification of the copulatory apparatus. Takayama and Okutani26 have also noted that the hectocotylised arm suckers have toothed margins in E. parva, but have smooth margins in Sepiola birostrata with which it is compared. Interestingly, as mentioned above, they also note that the inner two rows of the infundibulum of the club sucker rims bear rows of comb-like papillae in E. parva (referred to as S. parva in Takayama and Okutani26: Fig. 5) that are identical in appearance to those seen in E. pardalota (Reid39: Fig. 4d). It would be worthwhile to examine this character among other Euprymna species in a more comprehensive review of the genus.
Clear species misidentifications in the literature are also evident from our COI tree (see also Supplementary Note 1), and should be reconciled by further study. For example, samples from three Sepiola species (S. robusta Naef, 1912, S. intermedia Naef, 1912, and S. affinis Naef, 1912), all collected at Banyuls-sur-mer, have nearly identical COI markers together with a sample deposited as Heteroteuthis dispar (0–0.35% divergence). This limited nominally interspecific COI variation, however, is comparable to variation seen within many other species of the Sepiolidae (e.g., our Ryukyuan bobtail species), and suggests the need for a critical reexamination of these Mediterranean taxa to determine whether this seeming anomaly is due to misidentification, conspecificity among some taxa, recent divergence or a low mutation rate of this loci in some of these taxa. Conversely, we find extensive intra-specific COI variation within E. tasmanica from Australia, E. albatrossae from the Philippines and within the tropical bottletail squid S. kochii from Taiwan, Okinawa, and Japan.
These observations demonstrate either that molecular variation within bobtail squid species can be unusually large, or that some species will need to be further subdivided to reflect molecular variation within purported taxa. For example, Norman and Lu47 tentatively gave the distribution of E. tasmanica (with the type locality given by Pfeffer58 only as Bass Strait) as extending from the Great Australian Bight (southern Australia), Tasmania and extending along eastern Australia, possibly to as far north as Moreton Bay, Queensland. They recognized that an undescribed taxon with the same configuration of enlarged arm suckers occurs in northern Australia. The COI data presented here was obtained from supposed E. tasmanica over a wide distributional range, including Western Australia and New South Wales, so it may comprise more than a single species, particularly as many Australian marine taxa are southern Australian endemics. This taxon needs to be critically reexamined. The same may be true for animals ascribed to Sepidarium kochii.
Prior to the advent of molecular tools, Euprymna had been a particularly difficult group for morpho-taxonomists. Morphological redescription of all nominal Euprymna species to include additional characters for direct comparison (in addition to molecular traits) is essential. The reliance on the arrangement of enlarged arm suckers as almost the only distinguishing character is, of course, problematic. Future studies could usefully include additional characters such as sucker rim ultrastructure, spermatophore structure, and ontogenetic changes in enlarged sucker arrangement (i.e., to determine how fixed, or otherwise, is the pattern of enlargement at different stages of maturity), all of which appear to be differ to varying degrees but hard to compare at this time among all nominal species.
The dramatic differences between intra- and interspecific COI variation across the sepiolid tree point to the need for a comprehensive reevaluation of bobtail squid with both sequence markers and morphology to characterize the diversity and biogeography of this widely dispersed group. We have seen that limited RNA sequencing from optic lobe transcriptomes easily provides large numbers of robust molecular characters and can be used similarly in other group of cephalopods. Our transcriptome resources provide a foundation for comparative genomics and biology within this diverse group of cephalopods. Finally, the identification of three species of Ryukyuan bobtail squid raises interesting questions about the possible differing ecological roles played by these species.
Materials and methods
We surveyed bobtail squid along the Ryukyu archipelago from shallow waters to ~20 m depth. Sepiolid squid eggs and, where possible, adults, were obtained from several sites in Okinawa Island (from both the East China Sea and Pacific Ocean, from March to November in 2016 and 2017, and February to August in 2018), from one site in Ishigaki Island (July 2016), from one site in Kume Island (November 2018), and from Zamami Island (October 2016) in the Kerama Islands to the south (Fig. 1a). More sampling was done on the East China Sea side than the Pacific coast. Less extensive sampling around the Ryukyu islands was also conducted from February to November 2017 and February to August 2018. We also collected Sepiola parva in Sagami Bay, Tokyo (July 2017).
Adults were collected at night by hand while wading, snorkeling, or diving on SCUBA in shallow water (<2 m) off Okinawa at Miyagi Island (26.38N, 127.99E), Diamond Beach at Seragaki (26.51N, 127.88E), Motobu (26.60N, 127.91E), Sunabe Sea Wall (26.32N, 127.74E), Zamami Island (26.22N, 127.30E), and Kume Island (23.33N, 126.81E). Collection location details are shown in Table 2. Live animals were immediately brought to the culture facility at OIST (Okinawa Institute of Science and Technology) and acclimated for one hour by gradually replacing source water with aquarium water.
Eggs were collected during the day between 6 and 18 m at Seragaki (26.51 N, 127.88E), Gorilla Chop in Sakimotobu (26.63N, 127.88E), Motobu in the north of Nago Bay (26.60N, 127.91E), Mizugama (26.36N, 127.73E), Oura Bay (26.53N, 128.07E), Oganzaki at Ishigaki Island (24.44N, 124.07E), and Sunabe Sea Wall (26.33N, 127.74E) using SCUBA. Collections were made from March to November 2016 and unhatched eggs were not found after August. Stones were flipped at depths from 2 to 30 m, and all stones with eggs attached were found between 6 and 18 m.
Eggs were gently removed to a plastic container that was kept open upon ascending. They were then immediately taken to aquaria at OIST and acclimated as described for adults above. Eggs were kept in round containers with mesh bottoms inserted into two litre aquaria and exposed to a continuous water flow.
As a further aid in the sequence-based characterization of bobtail species, we also collected new samples from several previously described species: fourteen E. berryi from mainland Japan and Taiwan; five Euprymna scolopes from Honolulu, Hawaii (provided by Spencer Nyholm); five Sepiola parva from the Sagami Bay in Japan; seven Sepiola birostrata from Osaki Shimojima, in the Seto Inland Sea of Japan, Hyogo Prefecture, and Hokkaido Prefecture in the Japan Sea; and four putative Euprymna morsei from Mie Prefecture, Japan (Pacific Ocean) (later confirmed by sequence analysis, see below). One additional individual of the later species was obtained from Izu Chuo Aqua Trading Co., Ltd., and kindly provided by the Miller Unit at OIST. For use as outgroup taxa, we collected four bottletail squid, S. kochii (Sepiadariidae), from Mie prefecture, Okinawa, and Taiwan; and obtained one pyjama squid S. lineolata (Sepiadariidae) as a gift from the Monterey Bay Aquarium (captive bred). The identities of these samples were confirmed based on existing available molecular makers, and morphology. A complete list of COI samples used in this study is shown in Supplementary Table 2.
Collection of new specimens of Sepiola parva (E. parva comb nov.)
Type 2 squid conform in all respects to the species originally described, and recognized in the published literature, as Sepiola parva Sasaki 1913. According to Gleadall59, however, the type specimens of this species (reportedly housed in the MSUT (University Museum, University of Tokyo)) are missing and are presumed lost. For sequence and morphological comparison, we collected new specimens from Sagami Bay, close to the type locality of S. parva (Tokyo Bay), and confirmed their identity by COI and transcriptome markers (Figs. 2 and 3).
A semiclosed system of five 70 l tanks, five 2 l tanks, and 100 l sump was used. An ultraviolet sanitizing light, crushed coral, mesh filter, two protein skimmers, and chiller were used to maintain water quality. Light emitting diode (LED) aquarium lights provided a 12:12 light:dark photoperiod. A dim blue LED light was illuminated during the dark cycle to mimic moonlight. Sand-filtered seawater was provided weekly from a local source supplied by OIST Animal Support and was maintained at 24 °C. Water changes of 15% were performed weekly. Salinity averaged 35 parts per thousand (ppt) but ranged between 33–36 ppt. The pH was maintained between 8.00 and 8.15. Alkalinity, ammonia, and nitrate were measured three times per week using qualitative tests. Ammonia never exceeded 0.15 ppm and nitrate never exceeded 5 ppm. Sand was collected from where the animals were obtained and washed with deionized water prior to adding to the aquaria.
Paralarvae and juveniles were fed live wild-caught mysid shrimp, Neomysis sp. ad libitum twice daily. Mysids and wild-caught Palaemon sp. and Caridina sp. were provided to juveniles and adults.
Laboratory culture of Ryukyu type 1 (Euprymna sp.)
We found Ryukyuan Type 1 eggs near both Okinawa and the Ishigaki Islands. Type 1 hatchlings transcriptomes are distinct from those of known adult Indo-Pacific bobtail squid. In laboratory culture, Type 1 hatchlings are smaller than hatchlings of the other two types of Ryukyuan bobtail squid. Although hatchlings swim immediately upon hatching, and some feeding behavior was observed, no hatchling survived past 10 days. It is possible that in our culture they hatched prematurely, or that once hatched they lacked some environmental cue to properly develop their predatory behavior.
Laboratory culture of Ryukyu type 2 (E. parva comb. nov.)
We found Ryukyuan Type 2 bobtail squid in Okinawa (along the East China Sea), the Zamami Islands, and Miyagi Island (on the Pacific Ocean side). We raised Ryukyuan Type 2 to maturity in our laboratory, following culturing conditions described for other bobtail squid. Modifications include the use of a semiclosed system maintained at 23 °C, and an exclusive diet of mysid shrimp (Neomysis sp.). The life cycle, from hatching to sexual maturity to hatching of progeny, took approximately three months. The closure of the life cycle of Ryukyuan Type 2 will enable comparative analysis of behavior and physiology between the mainland Japanese and Ryukyuan populations. Further, E. parva’s small size at maturity, abundance throughout the year in easy to access areas, and simple diet promote this species as a viable option to study cephalopods in laboratory settings.
Laboratory culture of Ryukyu type 3 (E. brenneri)
We found Ryukyuan Type 3 bobtail squid in shallow waters off Okinawa Island (Seragaki on the East China Sea, and Oura Bay and Miyagi island on the Pacific coast), off Ishigaki Island to the south, and off the Penghu coastal waters of Taiwan (Fig. 1a). We raised Type 3 hatchlings to maturity in the laboratory, and observed mating behavior, but no eggs were laid. In captivity, hatchlings exhibit a paralarval stage similar to E. scolopes hatchlings20 and swim at the surface of the water column in a positive phototaxic manner both during simulated day and night photoperiods. Squids maintain a dark coloration with expanded chromatophores, except while preparing to capture their prey, at which point chromatophores contract and squids appear colorless. Adult mysids longer than 8 mm were hunted successfully on the fourth day post hatching. Squid were observed to seize they prey with their tentacles from below, holding it with their arms while eating. Settling and burying behavior was first observed at day five. Hatchlings periodically entered the water column until day 25 when all squids exhibited completely benthic lifestyles. Sexual dimorphism was visibly apparent at day 65 based on visual observation of the hectocotylus compared with non-hectocotylised left arm 1 in males. From day 65 males and females were separated in our cultures and brought together to test for mating behavior. Mating was achieved on day 83 and carried on for approximately 60 min. Mating behavior resembled previously described behavior in other Euprymna spp.20,60,61. After the last female died, unfertilized eggs were found inside her ovary. The longest-lived squid was a male that died on day 99.
COI sequencing and phylogeny
Genomic DNA was isolated using the MagAttract HMW DNA kit from small tissue samples taken from the arms of hatchlings or adults and the fins of randomly selected specimens in our tanks. The universal COI primers62 LCOI1940 5′-ggtcaacaaatcataaagatattgg-3′ and HCOI2198 5′-taaacttcagggtgaccaaaaaatca-3′ were used to obtain fragments of more than 574 bp. Polymerase chain reaction (PCR) was performed in a Bio-Rad T100™ Thermal Cycler with an initial denaturation at 94 °C for 1 min. followed by 30 cycles of 94 °C for 30 s., 42 °C for 1 min, 72 °C for 1 min; and a final extension at 72 °C for 10 min. PCR reactions were carried out in a total volume of 10 µL containing 3.0 µL of DNA template, 1.0 µL of 10× Taq Buffer, 0.8 µL of dNTPs (10 µM), 0.2 µL of each primer (10 µM), 0.25 U of Ex Taq (TAKARA) and 4.8 µL of D2W. PCR products were cleaned with ExoSAP-IT (Affymetrix/USB corporation) and then sequenced using a BigDye v3.1 Terminator Sequencing Kit (Applied Biosystems) using the LCOI1940 primer on a Genetic Analyzer (ABI 3130xl, Applied Biosystems).
In addition to the sequences we generated here, sepiolid COI sequences deposited in Genbank from several other studies were integrated into our analysis (Supplementary Table 1). A COI sequence from E. pardalota was included. The E. pardalota sequence data were obtained from a specimen collected in East Timor (note not the type locality) and lodged in the Australian Museum Collections (AM C.476100.002, EBU 80020).
Sequences were aligned in MAFFT v7.158b63 and the phylogenetic reconstruction was performed with IQ-tree software64 using maximum likelihood (ML) with 1000 ultrafast bootstrap replications65 and the best fit model determined by ModelFinder66.
RNA isolation and sequencing
We dissected the optic lobes from randomly selected hatchlings of our three Ryukyuan bobtail squids species and E. scolopes egg masses in our tanks, an embryo of S. lineolata and juveniles of Sepiola parva. Mantle muscle was also dissected from adult Sepiola birostrata, S. kochii, Euprymna berryi, and female putative Euprymna morsei. Details of the samples, collection locations, and tissue used are shown in Supplementary Data.
Total RNA was extracted with the RNeasy micro kit (Qiagen) and quantified by Qubit fluorometer (Invitrogen). RNA quality integrity numbers (RIN) were obtained using the Agilent 4200 TapeStation. cDNA was synthesized and barcoded, and RNAseq libraries were produced with the Illumina NeoPrep TrueSeq stranded mRNA library prep kit. Ten barcoded strand-specific libraries were pooled and sequenced in a single lane of Illumina HiSeq 4000 (paired end 2 × 150 bp sequences). In total, four lanes were sequenced.
In addition to the sequences generated here, we also used RNAseq data from E. tasmanica donated by Prof. Jan Strugnell from James Cook University.
Transcriptome analysis and orthology determination
Raw reads were visualized with FastQC (http://www.bioinformatics.babraham.ac.uk/projects/fastqc/). Removal of low quality reads and trimming of adapter sequences were performed in Trim Galore v. 0.4.0 (http://www.bioinformatics.babraham.ac.uk/projects/trim_galore/) with cutadapt67. De novo transcriptome assemblies were performed using Trinity68. We also used CD-HIT-EST69 to remove putative haplotype redundancy and keep the longest contigs. Open reading frames (ORFs) and coding sequences (CDS) were identified with Transdecoder v3.0.1 (http://transdecoder.github.io). Orthology assignment was performed with OMA stand-alone v.1.1.270 using default parameters and an all-against-all pairwise amino acid sequence comparison run in parallel on the Okinawa Institute of Science and Technology HPC cluster. From the OMA output, we used (1) the “OMA groups” or orthogroups provided in fasta format, where all pairs of genes within one group are orthologous to each other and each group contains one sequence per species, and (2) the all vs. all pairwise orthology inference in text format, from which the list of 1:1 orthology relationships were used for the Ks (synonymous substitution) distance determination (see details below).
Matrix construction and phylogenetic analysis
For phylogenetic analysis we extracted 452 orthogroups containing all 40 individuals from a total of 1325 unique orthogroups (containing at least our 19 Ryukyuan individuals) generated by OMA. Four different matrices were constructed using coding and peptide sequences, each pair set including 452 orthogroups (no missing taxa) and 1417 orthologous groups (including missing taxa). For this latter group, for each species we included the top 50% of individuals based on their orthogroup content. Amino acid and CDS were aligned in MAFFT v7.158b and trimmed using Gblock v0.91b71 allowing at most 50% gap positions prior to concatenation. The resulting data matrices consist of 136,333 (no missing data) and 413,030 (no missing data) positions for the amino acid and CDS set with no missing taxa, while on 514,512 (5.40% missing data) and 1,558,759 (5.39% missing data) positions for the amino acid and CDS set with missing taxa.
Maximum likelihood analyses were performed for the four matrices by using the IQ-tree software with an ultrafast bootstrap approximation of 1000 replicates, and the best model estimated by ModelFinder (-m MFP + MERGE) with the relaxed clustering algorithm (-rcluster 10)72 under the Bayesian Information criterion.
Bootstrap values above 95% were considered as highly supported. Trees based on nucleotide sequences showed almost all clades with high support (including all our species clades supported with 100% bootstrap).
Bayesian inference was performed in Exabayes v1.573 using two independent runs with four coupled chains each and the GTR + Γ model for each gene. Only the data matrix based on CDS with no missing taxa were used for the practical reason mentioned above. Each independent run was continued for 1 million generations, sampling every 500 until the average standard deviation of split frequency was <1%. The first 25% of samples were discarded as burn-in every 500 generations and proper sampling post burn-in was evaluated by an effective sample size (ESS) of >500.
Pairwise synonymous distance (Ks) calculation
Intra- and interspecific synonymous distance (Ks) were calculated using the Yang-Nielsen estimates from the yn00 program of PAML package 4.874. Using the OMA all vs. all pairwise orthology inference from Ryukyuan species and their congeners, we selected the median Ks values from each of the 1:1 orthologous gene pairs.
Divergence time estimation
Divergence times among the Ryukyuan species were estimated using the r8s v1.80 program75 with a local molecular clock. We used the maximum likelihood tree with branch length estimated from the IQ-tree software, based on ultrafast bootstrap with 1000 replicates. We included RNA-seq data of Idiosepius paradoxus Ortmann, 1888 (SRR2984343) and Sepia esculenta Hoyle, 1885 (SRR1386223), with a calibration of 174 Mya, the midpoint of the range (129, 219 Mya) from Supplementary Fig. 4 of Tanner et al.1, for the splits between Sepiidae with Idiosepiidae and the Sepiolidae.
Terminology, measurements, indices, and abbreviations for anatomical structures referred to in the new species description follow Roper and Voss76, with a few minor differences (Supplementary Table 4). In the current paper, ASC refers to the total number of suckers on each designated arm (this abbreviation refers to the number of suckers on the basal half of each arm in Roper and Voss76, with ASCT used for the total number of arm suckers). All measurements are in millimeters (mm). Measurements and counts for individual mature and sub-mature specimens are presented in Supplementary Table 3; the range of values for each character is expressed in the description as: minimum–maximum. The values for each sex are given separately. Only large specimens were measured, but only one (NSMT Mo 85891), a male, was fully mature.
Other abbreviations: AM, Australian Museum, Sydney; NSMT, National Museum of Science and Technology, Tokyo, Japan; ZMH, Zoologisches Museum, Universitat Hamburg.
For scanning electron microscopy, dissected tissues were mounted, then air dried and examined after gold coating in either a JEOL JSM 7100 FESEM Field Emission Scanning Electron Microscope, or a JOEL 6480LA SEM Tungsten Variable Pressure Scanning Electron Microscope.
Further information on research design is available in the Nature Research Reporting Summary linked to this article.
Study accession number for RNA sequencing: SRP157062. Accession numbers for COI sequences: LC417211–LC417235. Alignments, best partition scheme and models are available in Figshare https://figshare.com/s/94a59f3ce82cacabaa7c.
Tanner, A. R. et al. Molecular clocks indicate turnover and diversification of modern coleoid cephalopods during the Mesozoic Marine. Revolut. Proc. R. Soc. B 284, 20162818 (2017).
Franklin, A. M., Squires, Z. E. & Stuart-Fox, D. Does predation risk affect mating behavior? An experimental test in dumpling squid (Euprymna tasmanica). PLoS ONE 9, e115027 (2014).
Rodrigues, M., Garcí, M. E., Troncoso, J. S. & Guerra, A. Burying behaviour in the bobtail squid Sepiola atlantica (Cephalopoda: Sepiolidae). Ital. J. Zool. 77, 247–251 (2010).
Salazar, K. A., Joffe, N. R., Dinguirard, N., Houde, P. & Castillo, M. G. Transcriptome analysis of the white body of the squid Euprymna tasmanica with emphasis on immune and hematopoietic gene discovery. PLoS ONE 10, e0119949 (2015).
McFall-Ngai, M. Host-microbe symbiosis: the squid-Vibrio association—a naturally occurring, experimental model of animal/bacterial partnerships. Adv. Exp. Med. Biol. 635, 102–112 (2008).
Ruby, E. G. Lessons from a cooperative, bacterial-animal association: the Vibrio fischeri–Euprymna scolopes light organ symbiosis. Annu. Rev. Microbiol. 50, 591–624 (1996).
Zepeda, E. A., Veline, R. J. & Crook, R. J. Rapid associative learning and stable long-term memory in the squid Euprymna scolopes. Biol. Bull. 232, 212–218 (2017).
Sinn, D. L. & Moltschaniwskyj, N. A. Personality traits in dumpling squid (Euprymna tasmanica): context-specific traits and their correlation with biological characteristics. J. Comp. Psychol. 119, 99–110 (2005).
Sinn, D. L., Apiolaza, L. A. & Moltschaniwskyj, N. A. Heritability and fitness-related consequences of squid personality traits. J. Evol. Biol. 19, 1437–1447 (2006).
Sinn, D. L., Gosling, S. D. & Moltschaniwskyj, N. A. Development of shy/bold behaviour in squid: context-specific phenotypes associated with developmental plasticity. Anim. Behav. 75, 433–442 (2008).
Steer, M. A., Moltschaniwskyj, N. A., Nichols, D. S. & Miller, M. The role of temperature and maternal ration in embryo survival: using the dumpling squid Euprymna tasmanica as a model. J. Exp. Mar. Bio. Ecol. 307, 73–89 (2004).
Lee, P. N., Callaerts, P. & Couet, H. Gde The embryonic development of the Hawaiian bobtail squid (Euprymna scolopes). Cold Spring Harb. Protoc. 2009, db.ip77 (2009).
Callaerts, P. et al. HOX genes in the sepiolid squid Euprymna scolopes: implications for the evolution of complex body plans. Proc. Natl Acad. Sci. U. S. A. 99, 2088–2093 (2002).
Hartmann, B. et al. Pax6 in the sepiolid squid Euprymna scolopes: evidence for a role in eye, sensory organ and brain development. Mech. Dev. 120, 177–183 (2003).
Lee, P. N., Callaerts, P., Couet, H. Gde & Martindale, M. Q. Cephalopod Hox genes and the origin of morphological novelties. Nature 424, 1061 (2003).
Kerbl, A. et al. Micro-CT in cephalopod research: investigating the internal anatomy of a sepiolid squid using a non-destructive technique with special focus on the ganglionic system. J. Exp. Mar. Bio. Ecol. 447, 140–148 (2013).
Shigeno, S. & Yamamoto, M. Organization of the nervous system in the pygmy cuttlefish, Idiosepius paradoxus Ortmann (Idiosepiidae, cephalopoda). J. Morphol. 254, 65–80 (2002).
Yamamoto, M., Shimazaki, Y. & Shigeno, S. Atlas of the embryonic brain in the pygmy squid, Idiosepius paradoxus. Zool. Sci. 20, 163–179 (2003).
Yoshida, M. A. et al. Molecular evidence for convergence and parallelism in evolution of complex brains of cephalopod molluscs: insights from visual systems. Integr. Comp. Biol. 55, 1070–1083 (2015).
Hanlon, R. T., Claes, M. F., Ashcraft, S. E. & Dunlap, P. V. Laboratory culture of the sepiolid squid Euprymna scolopes: a model system for bacteria-animal symbiosis. Biol. Bull. 192, 364–374 (1997).
Iglesias, J., Fuentes, L. & Villanueva, R. Cephalopod Culture. (Springer Science & Business Media, 2014).
Jones, N. J. E. & Richardson, C. A. Laboratory culture, growth, and the life cycle of the little cuttlefish Sepiola atlantica (Cephalopoda: Sepiolidae). J. Shellfish Res. 29, 241–246 (2010).
Nateewathana, A. The Sepiolidae (Cephalopoda) of the Andaman Sea, Thailand, with description of Euprymna hyllebergi sp. nov. Spec. Publ. Phuket Mar. Biol. Cent. 17, 465–481 (1997).
Belcaid, M. et al. Symbiotic organs shaped by distinct modes of genome evolution in cephalopods. Proc. Natl Acad. Sci. USA 116, 3030–3035 (2019).
WoRMs Editorial Board (2018). World Register of Marine Species. Available from: http://www.marinespecies.orhttp://www.marinespecies.or at VLIZ. Accessed March 2, 2018. https://doi.org/10.14284/170 (2018).
Takayama, K. & Okutani, T. Identity of Sepiola parva Sasaki, 1913 and S. birostrata Sasaki, 1918 in the Northwest Pacific (Cephalopoda: Sepiolidae). Jpn. J. Malacol. 51, 203–214 (1992).
Coryell, R. L., Turnham, K., de Jesus Ayson, E. G. & Lavilla-Pltogo, C. Phylogeographic patterns in the Philippine archipelago influence symbiont diversity in the bobtail squid–Vibrio mutualism. Ecol. Evol. 2018, 7421–7435 (2018).
Dai, L., Zheng, X., Kong, L. & Li, Q. DNA barcoding analysis of Coleoidea (Mollusca: Cephalopoda) from Chinese waters. Mol. Ecol. Resour. 12, 437–447 (2012).
Gebhardt, K. & Knebelsberger, T. Identification of cephalopod species from the North and Baltic Seas using morphology, COI and 18S rDNA sequences. Helgol. Mar. Res. 69, 259–271 (2015).
Jones, B. W., Lopez, J. E., Huttenburg, J. & Nishiguchi, M. K. Population structure between environmentally transmitted vibrios and bobtail squids using nested clade analysis. Mol. Ecol. 15, 4317–4329 (2006).
Judkins, H. L., Vecchione, M. & Rosario, K. Morphological and molecular evidence of Heteroteuthis dagamensis in the Gulf of Mexico. Bull. Mar. Sci. 92, 51–57 (2016).
Kubodera, T. & Okutani, T. A new species of bobtail squid, Euprymna megaspadicea, from Okinawa, Japan. Venus J. Malacol. Soc. Jpn. 61, 159–168 (2002).
Kubodera, T. & Okutani, T. New additions of luminous bobtail squids to the Japanese cephalopod fauna (Sepiolida: Sepiolidae: Heteroteuthinae). Venus J. Malacol. Soc. Jpn. 69, 145–161 (2011).
Layton, K. K. S., Martel, A. L. & Hebert, P. D. N. Patterns of DNA barcode variation in Canadian marine molluscs. PLoS ONE 9, e95003 (2014).
Nishiguchi, M. K., Ruby, E. G. & McFall-Ngai, M. J. Competitive dominance among strains of luminous bacteria provides an unusual form of evidence for parallel evolution in sepiolid squid-Vibrio symbioses. Appl. Environ. Microbiol. 64, 3209–3213 (1998).
Nishiguchi, M. K., Lopez, J. E. & Boletzky, S. V. Enlightenment of old ideas from new investigations: more questions regarding the evolution of bacteriogenic light organs in squids. Evol. Dev. 6, 41–49 (2004).
Groenenberg, D. S. J., Goud, J., De Heij, A. & Gittenberger, E. Molecular phylogeny of North Sea Sepiolinae (Cephalopoda: Sepiolidae) reveals an overlooked Sepiola species. J. Molluscan. Stud. 75, 361–369 (2009).
Iguchi, A. & Hongo, C. Coral Reef Studies of Japan. (Springer, 2018).
Reid, A. Euprymna pardalota sp. nov. (Cephalopoda: Sepiolidae), a new dumpling squid from northern Australia. The Beagle. Rec. Mus. Art. Galleries North. Territory 27, 135–142 (2011).
Aungtonya, C., Nateewathana, A., Tendal, O. & Nabhitabhata, J. New records of the bobtail squid, Euprymna hyllebergi Nateewathana, 1997 with designation of a neotype. Phuket Mar. Biol. Cent. Res. Bull. 70, 15–27 (2011).
Norman, M. D., Nabhitabhata, J. & Lu, C. C. An updated checklist of the cephalopods of the South China Sea. Raffles Bull. Zool. 2016, 566–592 (2016).
Lindgren, A. R., Pankey, M. S., Hochberg, F. G. & Oakley, T. H. A multi-gene phylogeny of Cephalopoda supports convergent morphological evolution in association with multiple habitat shifts in the marine environment. BMC Evol. Biol. 12, 129 (2012).
Strugnell, J. & Nishiguchi, M. K. Molecular phylogeny of coleoid cephalopods (Mollusca: Cephalopoda) inferred from three mitochondrial and six nuclear loci: a comparison of alignment, implied alignment and analysis methods. J. Mollusca. Stud. 73, 399–410 (2007).
Takumiya, M., Kobayashi, M., Tsuneki, K. & Furuya, H. Phylogenetic relationships among major species of Japanese coleoid cephalopods (Mollusca: Cephalopoda) using three mitochondrial DNA sequences. Zool. Sci. 22, 147–155 (2005).
De Heij, A. & Goud, J. Sepiola tridens spec. nov., an overlooked species (Cephalopoda, Sepiolidae) living in the North Sea and north-eastern Atlantic Ocean. Basteria 74, 51–62 (2010).
Ota, H. Geographic patterns of endemism and speciation in amphibians and reptiles of the Ryukyu Archipelago, Japan, with special reference to their paleogeographical implications. Res. Popul. Ecol. 40, 189–204 (1998).
Norman, M. D. & Lu, C. C. Redescription of The southern dumpling squid Euprymna tasmanica and a revision of the genus Euprymna (Cephalopoda: Sepiolidae). J. Mar. Biol. Assoc. UK 77, 1109–1137 (1997).
Sasaki, M. A monograph of the dibranchiate cephalopods of the Japanese and adjacent waters. J. Coll. Agric. Hokkaido Univ. 20, 1–357 (1929).
Naef, A. Die cephalopoden. Fauna Flora Golf. Neapel. 35, 1–863 (1923).
Bello, G. A key for the identification of the Mediterranean sepiolids (Mollusca: Cephalopoda). Bull. Inst. Oceanogr. 16, 41–56 (1995).
Bello, G. Cladistic analysis of the Atlanto-Mediterranean sepiolines (Cephalopoda: Sepiolidae) based on morphological characters. Mem. del. Mus. Civ. di Stor. Nat. die Verona (2nd Ser.), Sez. Sci. della Vita 13, 81–85 (1998).
Young, R. E. Sepiolidae. Available at: http://tolweb.org/Sepiolidae. Accessed January 2, 2019.
Reid, A. & Jereb, P. Family Sepiolidae. In P. Jereb & C. F. E. Roper eds. Cephalopods of the world. An annotated and illustrated catalogue of cephalopod species known to date. Vol. 1. Chambered nautiluses and sepioids (Nautilidae, Sepiidae, Sepiolidae, Sepiadariidae, Idiosepiidae and Spirulidae). pp. 153–203 (FAO Species Cat. Fish. Purp. Rome, 2005).
Leach, W. E. Synopsis of the orders, families and genera of the class Cephalopoda. Zool. Misc. 3, 137–141 (1817).
Sasaki, M. Decapod cephalopods found in Japan (Sepiolidae). 25 (Tokyo Dobutsu Gakkai, 1913).
Allcock, A. L., Lindgren, A. & Strugnell, J. M. The contribution of molecular data to our understanding of cephalopod evolution and systematics: a review. J. Nat. Hist. 0, 1–49 (2014).
Lindgren, A. R., Giribet, G. & Nishiguchi, M. K. A combined approach to the phylogeny of Cephalopoda (Mollusca). Cladistics 20, 454–486 (2004).
Pfeffer, G. Die Cephalopoden des Hamburger Naturhistorischen Museums. Abhandlungen aus dem Geb. der Naturwissenschaften/hrsg. vom Naturwissenschaftlichen Ver. Hambg. 8, 1–30 (1885).
Gleadall, I. G. A note on the Cephalopoda type specimens in the Zoology Department of Tokyo University Museum. J. Molluscan Stud. 69, 375–380 (2003).
Nabhitabhata, J., Nilaphat, P., Promboon, P. & Jaroongpattananon, C. Life cycle of cultured bobtail squid, Euprymna hyllebergi Nateewathana, 1997. Spec. Publ. Phuket Mar. Biol. Cent. 66, 351–365 (2005).
Squires, Z. E., Norman, M. D. & Stuart-Fox, D. Mating behaviour and general spawning patterns of the southern dumpling squid Euprymna tasmanica (Sepiolidae): a laboratory study. J. Mollusca Stud. 79, 263–269 (2013).
Folmer, O., Black, M., Hoeh, W., Lutz, R. & Vrijenhoek, R. DNA primers for amplification of mitochondrial cytochrome c oxidase subunit I from diverse metazoan invertebrates. Mol. Mar. Biol. Biotechnol. 3, 294–299 (1994).
Katoh, K. & Standley, D. M. MAFFT Multiple sequence alignment software Version 7: improvements in performance and usability. Mol. Biol. Evol. 30, 772–780 (2013).
Nguyen, L.-T., Schmidt, H. A., von Haeseler, A. & Minh, B. Q. IQ-TREE: a fast and effective stochastic algorithm for estimating maximum-likelihood phylogenies. Mol. Biol. Evol. 32, 268–274 (2015).
Hoang, D. T., Chernomor, O., von Haeseler, A., Minh, B. Q. & Le, S. V. UFBoot2: improving the ultrafast bootstrap approximation. Mol. Biol. Evol. 35, 518–522 (2017).
Kalyaanamoorthy, S., Minh, B. Q., Wong, T. K. F., von Haeseler, A. & Jermiin, L. S. ModelFinder: fast model selection for accurate phylogenetic estimates. Nat. Methods 14, 587–589 (2017).
Martin, M. Cutadapt removes adapter sequences from high-throughput sequencing reads. EMBnet. J. 17, 10–12 (2011).
Grabherr, M. G. et al. Trinity: reconstructing a full-length transcriptome without a genome from RNA-Seq data. Nat. Biotechnol. 29, 644–652 (2011).
Fu, L., Niu, B., Zhu, Z., Wu, S. & Li, W. CD-HIT: accelerated for clustering the next-generation sequencing data. Bioinformatics 28, 3150–3152 (2012).
Altenhoff, A. M., Gil, M., Gonnet, G. H. & Dessimoz, C. Inferring hierarchical orthologous groups from orthologous gene pairs. PLoS ONE 8, e53786 (2013).
Castresana, J. Selection of conserved blocks from multiple alignments for their use in phylogenetic analysis. Mol. Biol. Evol. 17, 540–552 (2000).
Lanfear, R., Calcott, B., Kainer, D., Mayer, C. & Stamatakis, A. Selecting optimal partitioning schemes for phylogenomic datasets. BMC Evol. Biol. 14, 82 (2014).
Aberer, A. J., Kobert, K. & Stamatakis, A. ExaBayes: massively parallel bayesian tree inference for the whole-genome era. Mol. Biol. Evol. 31, 2553–2556 (2014).
Yang, Z. PAML 4: phylogenetic analysis by maximum likelihood. Mol. Biol. Evol. 24, 1586–1591 (2007).
Sanderson, M. J. r8s: inferring absolute rates of molecular evolution and divergence times in the absence of a molecular clock. Bioinformatics 19, 301–302 (2003).
Roper, C. F. E. & Voss, G. L. Guidelines for taxonomic descriptions of cephalopod species. Mem. Natl Mus. Vic. 44, 48–63 (1983).
Funding for this project was supported by the internal funds the Okinawa Institute of Science and Technology (OIST) Molecular Genetics Unit. D.S.R. acknowledges support from the Marthella Foskett Brown Chair in Biological Sciences (UCB). We also thank staff from the OIST DNA sequencing section, Onna, Okinawa for their help with the RNA-sequencing. We thank the Miller Unit at OIST for gift of E. morsei obtained from Izu Chuo Aqua Trading Co., Ltd.; Mong-Fong Lee from the National Penghu University of Science and Technology for samples of Euprymna berryi, Euprymnasp., and Sepiadarium kochii from Taiwan; Spencer Nyholm from the University of Connecticut for samples of E. scolopes; Bret Grasse from the Marine Biological Laboratory (MBL) for his sampling and donation of S. lineolata; Satoshi Tomano for samples of S. birostrata from the Seto Inland Sea; the Fisheries Cooperative Association of Kissa in Yamaguchi Prefecture through Hisayuki Abe for samples of E. berryi; Oshima Branch, the Tokyo Metropolitan Islands Area Research and Development Center of Agriculture, Forestry and Fisheries in Tokyo Metropolis through Kunihisa Yamaguchi for samples of E. parva; the Tajima Fisheries Technology Institute in Hyogo Prefecture through Tetsuya Ohtani for samples of Sepiola birostrata; the Fisheries Cooperative Association of Hamasaka in Hyogo Prefecture through Hiroshi Miyagai for samples of Rossia sp.; the Wakkanai Fisheries Research Institute in Hokkaido Government through Minoru Sano for samples of Sepiola birostrata; Hirohito Arima from Izuohshima Diving Center for samples and help during collection of E. parva; and Ryo Minemizu from Ryo Minemizu Photo Office for samples of Euprymna sp. from Kume Island. We are indebted to the late Sydney Brenner for his support and guidance. We wish to thank Michael Kuba, Spencer Nyholm, Bethany Rader, and Bret Grasse for their helpful advice on laboratory culture of cephalopods; Jan Strugnell for sharing the RNA-seq reads of E. tasmanica; Bernhard Hausdorf from the University of Hamburg Zoologishe Institut und Zookogishes Museum for the loan of the two Eupryma bursa syntypes, and Sue Lindsay and Chao Shen at Macquarie University, Sydney for assistance with Scanning Electron Microscopy, and Shawn Miller for the helpful information about marine life around Okinawa. Special thanks also to Giambattista Bello for his insightful and detailed comments and suggestions. Finally, we also want to thank the following people for their help during the sampling at different locations in Okinawa: Aki Masunaga and Keishu Asada from OIST, Ryoko Yanagisawa from the Diving team Snack Snufkin, Thoru Miyazato from the village office of Zamami, Thoru Kikuta from the Diving shop Hero, Taihei Matayoshi from Zamami sailing, and to Prof. Kaori Wakabayashi and her student Akari Yoshimoto from Hiroshima University.
The authors declare no competing interests.
Publisher’s note Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.
About this article
Cite this article
Sanchez, G., Jolly, J., Reid, A. et al. New bobtail squid (Sepiolidae: Sepiolinae) from the Ryukyu islands revealed by molecular and morphological analysis. Commun Biol 2, 465 (2019). https://doi.org/10.1038/s42003-019-0661-6
A lasting symbiosis: how the Hawaiian bobtail squid finds and keeps its bioluminescent bacterial partner
Nature Reviews Microbiology (2021)
Communications Biology (2021)