Larval and juvenile development of <Emphasis Type="Italic">Lestidiops sphyraenopsis</Emphasis> Hubbs, 1916 (Aulopiformes: Paralepididae) in the western North Pacific,with a reexamination of the holotype of <Emphasis Type="Italic">Stemonosudis molesta</Emphasis> (Marshall, 1955)

The early life stages of Lestidiops sphyraenopsis (Paralepididae) are described on the basis of 14 specimens [7.8 mm in notochord length (NL)–88.6 mm in standard length (SL)] collected from the western North Pacific, and the holotype of Stemonosudis molesta is reexamined. Larval L. sphyraenopsis occurred in the Kuroshio waters, and juveniles were taken in the Kuroshio–Oyashio transition waters. Diagnostic characters of larval and juvenile L. sphyraenopsis are 96–101 myomeres; 27–31 anal fin rays; 4–9 peritoneal pigment sections in larvae (7.8 mm NL–27.3 mm SL); dorsal and anal pigment patches present; and anus located anterior to a vertical through dorsal fin origin. Stemonosudis molesta, known only from the holotype from the South Pacific, is similar to immature specimens of L. sphyraenopsis, but can be clearly distinguished from the latter by having higher vertebral counts (105 vs. 96–101) and by morphometric and pigment differences. Consequently, S. molesta is a valid species, and the distribution of L. sphyraenopsis is restricted to the North Pacific.     

Recruitment of amphidromous sleepers Eleotris acanthopoma, Eleotris melanosoma, and Eleotris fusca into the Teima River, Okinawa Island

Recruitment courses of three amphidromous sleeper species, Eleotris acanthopoma, E. melanosoma, and E. fusca, were investigated at the surf zone adjacent to the river mouth and at five stations in the Teima River on Okinawa Island, Japan. All three species occurred at the surf zone as pelagic larvae with transparent and compressed body, a conspicuous air bladder, and an emarginated caudal fin. Eleotris fusca (16.0–19.6 mm in standard length: SL) sometimes possessed a vestige of the larval chin barbel and were larger than E. acanthopoma (9.7–13.2 mm SL) and E. melanosoma (11.2–12.8 mm SL). The pelagic larvae were also collected during full tide from the lower reaches of the tidally influenced area of the river. The pelagic larvae may be carried in and out of the estuary with some tidal fluxes, and they may settle when they reach the upper tidally influenced area where the salinity becomes extremely low. Body width and pigmentation of newly settled larvae increased. E. fusca was considered to migrate upstream to the freshwater area against the flow of the river just after reaching the settled stage. After settlement, all three species became completely pigmented, the caudal fin became round in shape, and the fin ray counts became complete with growth. Also, E. acanthopoma dispersed widely to the lower part of the tidally influenced area or to the lower reaches of the freshwater area, E. melanosoma dispersed to the lower part of the tidally influenced area, and E. fusca dispersed upstream.     

Larval and juvenile Polymetme elongata (Stomiiformes: Phosichthyidae) collected from Suruga Bay and offshore waters, Japan

Two larvae [17.4 mm standard length: SL (postflexion stage)] and 26.1 mm SL (transformation stage)] and a juvenile (31.7 mm SL) of a phosichthyid, Polymetme elongata, from Suruga Bay and offshore waters, central Japan, are described. These specimens had an elongate body with relatively short preanal length (53–63% SL), long anal fin base (2.6–3.4 times dorsal fin base length), and anal fin origin below dorsal fin base, and were further characterized by a blackish flap on each eye and internal clusters of melanophores (e.g., along caudal myosepta around midlateral line and on ventral margin of caudal peduncle). The short preanal length and larval melanophore pattern were very similar to those of another phosichthyid, Yarrella blackfordi, from the Atlantic Ocean.     

Larvae and juveniles of the plunderfishes <Emphasis Type="Italic">Artedidraco shackletoni</Emphasis> and <Emphasis Type="Italic">A.</Emphasis><Emphasis Type="Italic">skottsbergi</Emphasis> (Notothenioidei,Artedidraconidae) from the Indian sector of the Southern Ocean

Early life stages of Artedidraco skottsbergi and A. shackletoni were collected off Adélie Land. The morphology and pigmentation pattern of nine larvae and juveniles of A. skottsbergi between 17.2 and 21.4 mm in standard length (SL), and of two juveniles of A. shackletoni measuring 25.1 mm SL were described. A. skottsbergi was characterized by a heavily pigmented body, except for the caudal peduncle, with distinctively dense pigmentation on the ventrolateral half of the body and caudal section (17.2–17.9 mm SL). Furthermore, they had no pigmentation on the pectoral fin base until they attained 21.4 mm SL. Juvenile A. shackletoni had a heavily pigmented body except for the ventral side of the abdomen and the anal fin base. The proximal part of the dorsal fin and most of the anal fin were covered with melanophores. Although knowledge of larval and juvenile Artedidraco species is limited, the distribution of melanophores on the fins, pectoral fin base and caudal peduncle at each developmental stage may be useful for species identification.     

Early development of the endangered freshwater goby, Rhinogobius sp. BI (Gobiidae)

The early development of the endangered freshwater goby, Rhinogobius sp. BI (ogasawara-yoshinobori in Japanese), was described in the course of a serial rearing experiment over generations as ex situ preservation. The eggs, measuring 2.0 mm in long diameter and 0.7 mm in short diameter, were elliptical with a colorless transparent chorion, a slightly yellowish yolk, and some oil globules. Hatching occurred naturally at 6 to 7 days after spawning at 24.0°C. Newly hatched larvae, measuring 3.2–3.4 mm in total length (TL), had opened mouth and a globular yolk sac. The yolk was completely absorbed at 3.5 mm TL (5 days after hatching). Notochord flexion initiated at 5.7 mm TL (18 days) and finished at <9.1 mm TL (30 days). First dorsal fin began to form in postflexion larvae at 10.0 mm TL (40 days), and a full complement was attained at 11.6 mm TL (45 days). Second dorsal fin emerged at 5.7 mm TL (18 days); full count was attained and segmentation initiated at 9.1 mm TL (30 days). Anal fin anlage appeared at 5.7 mm TL (18 days); its ray count was completed and segmentation initiated at 9.1 mm TL (30 days), and branching at 15.6 mm TL (60 days). Caudal fin support appeared at 4.5 mm TL (15 days); segmentation initiated at 6.0 mm TL (24 days) and branching at 10.0 mm TL (40 days). Fanlike pectoral fin present in newly hatched larvae. Pectoral fin rays appeared at 10.0 mm TL (40 days), and its ray count completed at 15.6 mm TL (60 days). Pelvic fin projected at 9.1 mm TL (30 days), and a sucking disc partially formed at 11.6 mm TL (45 days). Aggregate numbers of all fin rays were completed at 15.6 mm TL in 60 days after hatching. Pelagic period continued for about 40 days, and settlement was completed in postflexion larvae at 45 days.     

The early life history of kurosoi,Sebastes schlegeli (Scorpaenidae), in the Sea of Japan

Larval and juvenile stages of kurosoi,Sebastes schlegeli, are described and illustrated from wild specimens. Some ecological aspects of larvae and juveniles are also described. Notochord flexion occurred between 5.6–7.5 mm SL. Transformation occurred between 13–20 mm SL. Preflexion and flexion larvae ofS. schlegeli can be distinguished from similar larvae by the pigmentation of the dorsal and ventral midlines of the tail and absence of pigmentation on the ventral portion of the rectum. After notochord flexion, the dorsal and lateral regions in both larvae and pelagic juveniles were heavily pigmented, suggesting adaptation for neustonic life style. Larvae and juveniles were caught at many coastal stations, but did not occur in cooler offshore waters. Larvae smaller than 20 mm SL inhabited surface waters. Until ca. 40 mm SL, juveniles inhabited mainly surface waters (without drifting seaweed), but also used other habitats, such as the drifting seaweed, and near the sea bed. Small larvae (<7 mm SL) fed mainly on copepod nauplii. Larger larvae fed on calanoid copepodites andEvadne nordmanni. Pelagic juveniles fed mainly on fish eggs, with fish larvae also being important food items for some individuals. Most food items taken by juveniles that were associated with drifting seaweed were eggs with attaching filaments (Cololabis saira andHyporhamphus sajori), suggesting that the high density of such food items both attracts and keeps juveniles around drifting seaweed.     

Developmental morphology of the Indian cyprinid fish Barilius canarensis

Embryonic and larval development of an Indian cyprinid fish, Barilius canarensis, is described from laboratory-reared specimens. The eggs, measuring 2.1–2.4 mm in diameter, were demersal, almost spherical in shape, transparent and unpigmented, with a pale yellow yolk without oil globules. Hatching occurred 39–45 h after fertilization at 26.8°–27.4°C. The newly hatched larvae, measuring 4.8–5.1 mm in body length (BL) with 22 + 17 = 39 myomeres, were characterized by melanophores already deposited on the eyes. The eggs of B. canarensis resembled those of the related danionin species Candidia barbatus, Opsariichthys uncirostris uncirostris, Zacco platypus, Z. sieboldii, and Z. temminckii. Although the larvae of B. canarensis were also similar to those of the foregoing species in general morphology, they differed in having a straight notochord tip and pigmentation on the eyes at hatching and the almost entire absence of melanophores on the ventral body surface from the yolk sac to postflexion larval stages. Conversely, melanophores occurred on the anterior abdominal and pericardial cavities from the preflexion to postflexion larval stages.     

Growth and morphological development of laboratory-reared larval and juvenile three-spot gourami <Emphasis Type="Italic">Trichogaster trichopterus</Emphasis>

Morphological development, including the body proportions, fins, pigmentation and labyrinth organ, in laboratory-hatched larval and juvenile three-spot gourami Trichogaster trichopterus was described. In addition, some wild larval and juvenile specimens were observed for comparison. Body lengths of larvae and juveniles were 2.5 ± 0.1 mm just after hatching (day 0) and 9.2 ± 1.4 mm on day 22, reaching 20.4 ± 5.0 mm on day 40. Aggregate fin ray numbers attained their full complements in juveniles >11.9 mm BL. Preflexion larvae started feeding on day 3 following upper and lower jaw formation, the yolk being completely absorbed by day 11. Subsequently, oblong conical teeth appeared in postflexion larvae >6.4 mm BL (day 13). Melanophores on the body increased with growth, and a large spot started forming at the caudal margin of the body in flexion postlarvae >6.7 mm BL, followed by a second large spot positioned posteriorly on the midline in postflexion larvae >8.6 mm BL. The labyrinth organ differentiated in postflexion larvae >7.9 mm BL (day 19). For eye diameter and the first soft fin ray of pelvic fin length, the proportions in laboratory-reared specimens were smaller than those in wild specimens in 18.5–24.5 mm BL. The pigmentation pattern of laboratory-reared fish did not distinctively differ from that in the wild ones. Comparisons with larval and juvenile morphology of a congener T. pectoralis revealed several distinct differences, particularly in the numbers of myomeres, pigmentations and the proportional length of the first soft fin ray of the pelvic fin.     

Early life history of kitsune-mebaru,sebastes vulpes (scorpaenidae), in the sea of japan

The larval and juvenile stages of kitsune-mebaru,Sebastes vulpes, based on 50 wild specimens collected in, the Sea of Japan, are described and illustrated, and some ecological aspects of the early life history (feeding, horizonal distribution and habitat shift) included. Preflexion larvae became extruded between 3.9–4.6 mm body length (BL) and notochord flexion occurred between 4.7–7.1 mm BL. Transformation from postflexion larvae to pelagic juventiles occurred between 13–17 mm BL. Compared with other rockfish species,S. vulpes is deep-bodied, throughout both larval and, juvenile stages. Larval and juvenileS. vulpes inhabit mainly coastal water surface layer (usually on the continental shelf), but do not occur offshore region (northwest of Oki Islands). Although someS. vulpes juveniles are associated with drifting seaweed, such clumps are not indispensable habitats for any stages. Surface-to-benthie migration of juveniles occurs at about 25 mm BL. Preflexion and flexion larvae feed mainly on copepod nauplii, and postflexion, transforming larvae and pelagic juveniles mainly on calanoid copepodites (Parracalanus parvus).     

Development of Sebastes taczanowskii (Scorpaenidae) in the Sea of Japan off Hokkaido with a key to species of larvae

The larval and juvenile stages of Sebastes taczanowskii (Japanese name: Ezo-mebaru) are described and illustrated based on 33 wild specimens [7.1–26.9 mm in body length (BL)] collected in the Sea of Japan, and eight specimens of reared larvae extruded from the one specimen of a captive pregnant female. Larvae were extruded between 4.3–5.0 mm BL and notochord flexion occurred 5.7–9.0 mm BL. Transformation from postflexion larvae to pelagic juveniles occurred between 13 and 17 mm BL. Preflexion and flexion larvae have a single melanophore row on the dorsal surface on the tail, and an internal line of melanistic dashes on the ventral side of the tail. Lateral pigmentation of postflexion and transforming larval body surfaces are light. Compared with other Japanese rockfish species, S. taczanowskii is shallow-bodied throughout both larval and juvenile stages. We provide an identification key to preflexion and flexion stage rockfish larvae found around the Japanese archipelago, and comparisons with other species. Larval and juvenile S. taczanowskii occurred in both near-shore and relatively offshore water around Shakotan Peninsula-Ishikari Bay, Hokkaido in June and July.     

Developmental morphology of the cyprinid fish Tanichthys albonubes

Embryonic, larval, and juvenile development of a small cyprinid species, Tanichthys albonubes, is described from laboratory-reared specimens. The eggs, measuring 1.0–1.2 mm in diameter, were demersal, almost spherical in shape, transparent and unpigmented, with a pale yolk without oil globules. Hatching occurred 45–53 h after fertilization at 25.5°–26.9°C. The newly hatched larvae, measuring 2.2–2.6 mm in body length (BL), had melanophores on the head and body. In particular, a dark vertical streak occurring posterior to the otic capsule and melanophores above the eyes were distinctive. The yolk was completely absorbed at 3.4 mm BL. Notochord flexion was initiated at 5.0 mm BL and finished at 6.0 mm BL. Aggregate numbers of all fin rays were completed at 11 mm BL. Squamation was initiated at 8.4 mm BL and completed at 13 mm BL. Although the eggs of T. albonubes resembled those of other small danionin species, including Aphyocypris chinensis, Chela dadiburjori, Danio rerio, Devario malabaricus, Gobiocypris rarus, Hemigrammocypris rasborella, and Horadandia atukorali, they differed from those of A. chinensis, C. dadiburjori, G. rarus, and Horadandia atukorali in having a wider perivitelline space. The larvae and juveniles of T. albonubes were similar to those of the aforementioned seven species plus Danio albolineatus, Danio kerri, and Devario sp. (cf. D. aequipinnatus) in general morphology. However, the early life stage morphology of T. albonubes differed from them in having a dark vertical streak posterior to the otic capsule and melanophores above the eyes in the yolk sac larval stage, and a dark lateral streak with an unpigmented area just above the former on the body, a dark blotch on the caudal fin, and reddish dorsal, anal, and caudal fins during the postflexion larval and juvenile stages.     

Juvenile morphology and occurrence patterns of three Butis species (Gobioidei: Eleotridae) in a mangrove estuary, southern Thailand

Juveniles of three eleotrid Butis species (B. butis, B. humeralis, and B. koilomatodon) are described; their occurrence patterns were examined in Sikao Creek, a mangrove estuary located in southern Thailand. Juveniles of each species were distinguished by the following characters: B. butis with no bands on body and pale pelvic fins; B. humeralis with no bands on body and densely pigmented pelvic fins; and B. koilomatodon with 5–6 regular bands on body and a fleshy process (preorbital knob) on the snout. Although B. butis shared the aforementioned characters with B. amboinensis found in the same estuary, the former was distinguished from the latter by having a greater number of pectoral fin rays (18–21 vs. 17) and a deeper caudal peduncle. Distribution patterns of the three Butis species in Sikao Creek were distinguishable from each other. Smaller B. butis [mean ± SD = 22.7 ± 16.9 mm in standard length (SL), n = 32] occurred in the upper reach of the estuary, while larger specimens (52.4 ± 26.2 mm SL, n = 18 and 51.5 ± 29.7 mm SL, n = 10, respectively) were found in the middle and lower reaches and none in the marine area. In B. humeralis and B. koilomatodon, only juveniles were caught except for one adult specimen each. Juveniles (8.9–16.5 mm SL, n = 79) of B. humeralis occurred in the upper and middle reaches and the marine area. B. koilomatodon juveniles (9.9–13.7 mm SL, n = 30) were distributed in all areas from the lower to upper reaches.     

Growth and morphological development of laboratory-reared larval and juvenile climbing perch <Emphasis Type="Italic">Anabas testudineus</Emphasis>

Morphological development, including fin and labyrinth organ, body proportions and pigmentation, in laboratory-reared larval and juvenile climbing perch Anabas testudineus was described and behavioral features under rearing condition were observed. Body lengths (BL) of larvae and juveniles were 1.9 ± 0.1 (mean ± SD) mm just after hatching (day-0), 8.7 ± 1.3 mm on day-19, reaching 18.4 ± 2.1 mm on day-35 after hatching. Aggregate fin ray numbers attained full complements in juveniles larger than 8.3 mm BL. Preflexion larvae started feeding on day-2 following formation of the upper and lower jaws, the yolk being completely absorbed by day-7 after hatching. Teeth appeared in flexion larvae larger than 5 mm BL on day-6, with cannibalism starting shortly after and continuing with further growth. Melanophores on the body increased with growth, a large dark spot developing on the lateral midline around caudal margin of the body in the postflexion and juvenile stages. The labyrinth organ differentiated in postflexion larvae larger than 7.2 mm BL on day-16, with air-breathing starting at the same time. Body proportions attained constant in postflexion larvae larger than 7.0 mm BL, and habitat of fish shifted from bottom to mid-layer. With the exception of fin ray numbers, the above morphological developments corresponded to behavioral shifts that occurred in the postflexion stage (ca. 7 mm BL), their subsequent continuity illustrating that the species possessed most juvenile-equivalent functions from ca. 7 mm BL.     

Dolichopteryx minuscula, a new species of spookfish (Argentinoidei: Opisthoproctidae) from the Indo-West Pacific

A new species Dolichopteryx minuscula is described on the basis of three specimens [49.4–59.6 mm in standard length (SL)] collected from the Indo-West Pacific. The new species is characterized by pouchlike eyes with a small lens (lens diameter 2.2% SL), an adipose fin, the anal fin base originating posterior to the dorsal fin base, and 16–17 (= 5–6 + 1 + 10–11) gill rakers. Total fecundity was relatively low, only 658 ova being obtained from one specimen, despite the ovary being mature. Ovarian eggs were clearly subdivided into “undeveloped” (0.1–0.7 mm diameter classes, n = 561) and “developed” (1.0–1.3 mm classes, n = 97) groups, based on their frequency distribution. Such relatively low fecundity and frequency distributions of ovarian eggs suggest that Dolichopteryx species spawn iteratively during spawning season.     

Developmental morphology of the cyprinid fish, Candidia barbatus

 Embryonic, larval, and juvenile development of a Taiwanese cyprinid fish, Candidia barbatus, is described from laboratory-reared specimens. The eggs, measuring 1.8–2.1 mm in diameter, were demersal, almost spherical in shape, transparent and unpigmented, with a pale yellow yolk and no oil globule. Hatching occurred 56–69 h after fertilization, the newly hatched larvae measuring 4.9–5.3 mm in body length (BL) with 25–26 + 13–14 = 39–40 myomeres. The yolk was completely absorbed at 7.6 mm BL. Notochord flexion was initiated at 6.8 mm BL and finished at 7.6 mm BL. Aggregate numbers of all fin rays were completed at 12 mm BL. Barbels on the upper jaw appeared near the corner of the mouth at 17 mm BL. Eggs of the species closely resembled those of its related cyprinid genera, Opsariichthys and Zacco. Larvae and juveniles of C. barbatus were similar to those of O. uncirostris subspp., Z. platypus, and Z. pachycephalus, but differed from the latter in the process of disappearance of the adipose finfold (postflexion larval stage), barbels on upper jaw (juvenile stage), and pigmentation on the lateral body surface (postflexion larval and juvenile stages). Although C. barbatus also differed from the Z. temminckii species' group [Z. temminckii and Zacco sp. (sensu Hosoya, 2002)] in having barbels, larvae and juveniles of the former showed more similarity to the latter species group than to O. uncirostris subspp., Z. platypus, and Z. pachycephalus, from the aspect of head and body pigmentation.     

Redescription of <Emphasis Type="Italic">Bregmaceros mcclellandi</Emphasis> Thompson, 1840 (Gadiformes: Bregmacerotidae)

 This study redescribes Bregmaceros mcclellandi Thompson, 1840, based on one specimen (74.4 mm SL) from the Bay of Bengal and 66 specimens (30.0–84.7 mm SL) from Mumbai (Bombay), India, because the type specimens have apparently been lost. The present specimens are characterized by having black dorsal, pectoral, and caudal fins and show the following morphology: caudal fin slightly forked; body chromatophores present mainly at the dorsal part; no scales on cheek; vertebrae 52–55 (13–15 + 38–41); dorsal rays 52–59; anal rays 54–60; pectoral rays 18–20; caudal rays 27–31 (principal rays 14); transverse scales 14–15. In the 66 Mumbai specimens, it was confirmed that the distinctive black fin pigmentation developed sequentially with growth, with complete pigmentation first on the anterior lobe of the dorsal fin, then simultaneously on the posterior lobe of the dorsal fin, the caudal fin, and the pectoral fin, and last, on the anal fin. This species is known only from the Arabian Sea, Bay of Bengal, and Gulf of Thailand. A review of 16 nominal Bregmaceros species indicates that, besides B. mcclellandi, the distinctive dark fin pigmentation is found in B. atripinnis (Tickell), B. atlanticus Goode and Bean, B. japonicus Tanaka, and B. lanceolatus Shen. B. atripinnis is considered a junior synonym of B. mcclellandi, and the others are clearly distinct from B. mcclellandi. Comments are made on some of the characters to more fully characterize the species and for reference in future revisionary and phylogenetic studies. Received: June 17, 2002 / Revised: December 2, 2002 / Accepted: December 24, 2002     

Early ontogeny of a South Pacific gonostomatid fish <Emphasis Type="Italic">Sigmops longipinnis</Emphasis>

 During the R/V Hakuho-maru Cruise KH-95-2, Ocean Research Institute, University of Tokyo, from Tokyo, Japan to the South Pacific east of Australia (22° N–30° S; 126° E–176° E) from June to September, 1995, 77 unidentified gonostomatid larvae (5.5–20.0 mm SL) were collected south of 20° S with an IKMT net. They subsequently were identified as Sigmops longipinnis (Mukhacheva), and its ontogeny during the latter part of the larval stage (body form and proportions, photophores, pigmentation, and meristics) is described here. The larvae develop a species-specific row of melanophores along the midlateral line anterior to the caudal peduncle and another along the middorsal line from before the dorsal fin to just before the caudal fin. Received: June 24, 2002 / Revised: November 2, 2002 / Accepted: January 31, 2003     

Remarkable ophidiid larva (Neobythitinae) from New Guinean waters

A new type of ophidiid larva referred to the Neobythitinae is described on the basis of one specimen (22.5 mm in standard length: SL) found in the “Dana” flatfish larval collection from New Guinean waters. It is characterized by a very high body (ca. 48% SL), with a single elongate first dorsal-fin ray and protruding abdominal cavity with a long fleshy appendage at its posteroventral end. Generic and specific affinities of the larva are discussed. It is supposed that the larva belongs to one of the Pycnocraspedum species, probably to P. squamipinne.     

Pelagic juvenile of <Emphasis Type="Italic">Halargyreus johnsonii</Emphasis> (Gadiformes: Moridae) from Suruga Bay,Japan

 A pelagic juvenile (43.0 mm standard length) of the deep-sea gadiform fish Halargyreus johnsonii was collected by a larva net towed at depths from 200 m to 90 m at Suruga Bay, Japan. The specimen had an elongate body, eyes located dorsally on the head, a depressed anal fin, small bony tubercles on the lower jaw symphysis, elongate pelvic fin rays, and a pointed caudal fin. The body was silver with numerous small black spots. The gut was filled with a copepod, Pareuchaeta russelli, that is characterized by a surface to mesopelagic distribution. Received: May 30, 2002 / Revised: December 16, 2002 / Accepted: December 24, 2002     

Larvae of <Emphasis Type="Italic">Lamprogrammus shcherbachevi</Emphasis> (Ophidiiformes: Ophidiidae) from the western North Pacific Ocean

Three exterilium larvae (18.2 mm notochord length to 113.3 mm standard length) of an ophidiid, Lamprogrammus shcherbachevi, from the western North Pacific are described. The specimens had a highly specialized morph with a remarkably elongate trailing gut and ventral coracoid process, and many elongate anterior dorsal fin rays, as occur in other exterilium larvae, but were characterized by unique melanophore patterns (a cluster of melanophores on the back of the stalked pectoral fin base, a row of clusters midlaterally on the trunk and caudal region, and further clusters on the trailing gut). Although the largest specimen (113.3 mm standard length, much larger than the previously recorded maximum size of exterilium larvae) retained typical features of the exterilium stage, the ventral coracoid process was significantly reduced in size compared with that of a smaller specimen (37.8 mm standard length). Comparison of the largest specimen with an adult suggests that the anterior dorsal fin rays would disappear during the transformation stage.