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.     

External Morphology of Lophiosilurus alexandri Steindachner, 1876 during Early Stages of Development,and Its Implications for the Evolution of Pseudopimelodidae (Siluriformes)

Pseudopimelodidae are Neotropical catfishes characterized by having slightly to strongly depressed body in fully developed specimens. The largest species of the family with 500 mm SL, Lophiosilurus alexandri, experiences impressive changes in body shape during development, becoming extremely depressed when fully developed. Accordingly, Lophiosilurus alexandri is an ideal species to observe the morphological changes during ontogeny, and to seek solid interpretations on the polarity of characters. Specimens of distinct larval periods (yolk sac, flexion and postflexion; n = 186 specimens) and juvenile stages (n = 20) were analyzed. Changes in body shape, position of mouth and eye, morphology of fins and pigmentation were observed during the development of Lophiosilurus. Larvae (5.7–11.2 mm standard length) had pigmentation concentrated on the head and parts of body, eyes small and pigmented, short barbels, and well-developed finfold. Juveniles (15.9–28.1 mm standard length) had body shape similar to adult, with head depressed and bearing bony ridges, large mouth, dorsally-oriented eyes, small barbels and well-developed shoulder bulges (cleithral width). The greatest morphological changes in the development of L. alexandri occurred during the postflexion larval stage. Relative to standard length, measurements of snout length, head depth and body depth are smaller in juveniles than in larvae, but body width is larger. New interpretations on the phylogenetic characters related to these changes are provided in view of the two alternative hypotheses of the evolution of Pseudopimelodidae.     

Notes on the morphology of the early stage of the rare bramid genus Eumegistus

The morphology of the early stage of Eumegistus was described from three specimens [E. brevorti: 23.0 mm in standard length (SL) juvenile; E. illustris: 5.8 mm SL postflexion larva, and 40.0 mm SL juvenile] recently rediscovered in museum collections. Larval and juvenile pigmentation patterns were reported for the first time for this genus. The 5.8 mm SL postflexion larva of E. illustris had pigmentation on the head and anterior half of the body, through to the middle of the dorsal fin base. In larvae and juveniles of both species, the outer side of the pelvic fin was pigmented. The two juveniles possessed several spines on the lachrymal and protruding rays in the middle of the caudal fin. Although it is known previously that the notochord flexion occurs at 5.0–6.0 mm SL in E. brevorti, the reexamined 5.0 mm SL specimen had the notochord completely flexed. Furthermore, we could not confirm whether the previously studied 4.0 mm SL specimen was E. brevorti because it was badly damaged.     

Description of transformation larvae and a juvenile of the dextral flounder,poecilopsetta praelonga (pleuronectidae, poecilopsettinae) from the northwestern waters of australia

Three late metamorphic transformation larvae ofPoecilopsetta praelonga (68.0–82.3 mm SL) and a juvenile (92.7 mm SL) captured from the waters off northwestern Australia (400–460 m deep) are described. The transformation larvae ofP. praelonga are distinguishable from the congeners of the same stage in having relatively low body depth (2.20–2.44 in SL), relatively large maxilla extending to anterior one-third of lower eye, and seven and six distinct spots along the dorsal and ventral margins of ocular side body, respectively. In the smallest specimen, the intestine was expanded posteriorly beyond the posterior wall of visceral cavity, but not in the larger specimens. The pectoral fin rays and the spines of scales were supposed to begin to be formed by about 80 mm SL. Ontogenetic changes which include decreasing ratios of upper jaw length to head length. and increasing ratios of depth of body muscle to body depth, were observed, based on a comparison of transformation larvae, a juvenile and adults.     

Early ontogeny of the big roughy Gephyroberyx japonicus (Beryciformes: Trachichthyidae) in captivity

Development of eggs and larvae of the big roughy Gephyroberyx japonicus are described on the basis of specimens reared in captivity. Spherical eggs (diameter 1.26–1.35?mm) with a single oil globule were pelagic. Newly hatched larvae (2.8–3.1?mm in body length, BL) had strong linear pigmentation on the head and trunk. The mouth opened at ca. 3.5?mm BL; thereafter the yolk was absorbed. Notochord flexion started at ca. 4.5?mm BL when body depth increased rapidly, and melanophores spread to all of the body. Notochord flexion was completed at ca. 5.0?mm BL. Head spination and pelvic fins began to develop during the flexion stage.     

Characterization of the initial ontogeny of Leiarius marmoratus (GILL, 1870): larvae to juvenile

Aiming to provide data on the biology of Leiarius marmoratus, which will aid in its production in captivity, as well as in studies for its preservation in the environment, this work had as objectives: analyze and describe main morphological alterations during larval ontogeny of the species. We analyzed 205 individuals, obtained by induced reproduction (Colpani Pisciculture) and kept in CEPTA/ICMBIO, Pirassununga, São Paulo, Brazil. Analyses were performed from hatching moment to 30th day. The specimens were classified into two periods: larval (Stages: vitelline, pre‐flexion, flexion, post‐flexion) and juvenile. Hatched larvae showed ident chromatophores only at anterior and posterior extremities of yolk sac. The standard length ranged from 2.16 mm (yolk) to 28.84 mm (Youth). Dorsal fin rays were initially observed at flexion stage (12–14 rays). Major alterations occurred during post‐flexion/juvenile stage, when dorsal, pectoral, pelvic, anal, and caudal fins were observed and pigmentation intensified throughout the lateral region, forming bands in the body, one between the end of the head and beginning of dorsal to pelvic fin, and another one beginning at dorsal to caudal peduncle and four longitudinal at the head.     

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.     

Morphological development and allometric growth patterns in hatchery-reared California halibut larvae

Morphological development, allometric growth and behaviour of hatchery-reared California halibut Paralichthys californicus were studied from hatching to metamorphosis (42 days post hatch, dph) at 187° C. Mean standard length ( L _S) of larvae and juveniles increased from 2.1 mm at hatching to 10.5 mm at metamorphosis with the increase in length being approximately linear. Stages of morphological development were described using the alphabetic staging (A–I) used for other flatfish species. Organogenesis and differentiation were more rapid and complex in yolk-sac (hatching, stage A–3 dph, stage B), preflexion (3–19 dph, stages B–C), and flexion larvae (from 20 to 23 dph, stages D–E), as larvae developed most of their sensory, feeding, respiratory and swimming systems. After notochord flexion at 24–25 dph (stage F), most morphological changes were related to the progressive transformation from a bilateral symmetrical larva to an asymmetrical benthic juvenile (42 dph, stages G–I).     

Early life history of mebaru,sebastes inermis (scorpaenidae), in sendai bay, japan

The early life history of the viviparous scorpaenid,Sebastes inermis, in Sendai Bay, Japan, was studied and early development described. Newborn preflexion larvae ofS. inermis were about 5.2 mm BL. Notochord flexion occurred at 5.4–8.0 mm BL and transformation at 14–20 mm BL. Preflexion and flexion larvae ofS. inermis were distinguished from similar larvae by the pigmentation pattern along the dorsal and ventral midlines of the tail. Pigmentation inS. inermis was light throughout the larval and early juvenile periods. Planktonic larvae were particularly abundant in coastal waters of Sendai Bay but not offshore. Vertical and horizontal larval sampling indicated that early larvae occupied near surface waters and horizontal larval sampling indicated that early larvae shift to a benthic habitat occurred at about 12 mm BL, at the end of the postflexion larval period.Sebastes inermis do not have a distinct pelagic juvenile stage, unlike many North Pacific species ofSebastes.     

Allometric growth and larval development in Pacific red snapper Lutjanus peru under culture conditions

Allometric growth is a common feature during fish larval development. It has been proposed as a growth strategy to prioritize the development of body segments related to primordial functions like feeding and swimming to increase the probability of survival during this critical period. In the present study we evaluated the allometric growth patterns of body segments associated to swimming and feeding during the larval stages of Pacific red snapper Lutjanus peru. The larvae were kept under intensive culture conditions and sampled every day from hatching until day 33 after hatching. Each larva was classified according to its developmental stage into yolk-sac larva, preflexion larva, flexion larva or postflexion larva, measured and the allometric growth coefficient of different body segments was evaluated using the potential model. Based on the results we can infer the presence of different ontogenetic priorities during the first developmental stages associated with vital functions like swimming during the yolk-sac stage [total length (TL) interval = 2.27–3.005 mm] and feeding during the preflexion stage (TL interval = 3.007–5.60 mm) by promoting the accelerated growth of tail (post anal) and head, respectively. In the flexion stage (TL interval = 5.61–7.62 mm) a change in growth coefficients of most body segments compared to the previous stage was detected, suggesting a shift in growth priorities. Finally, in the postflexion stage (TL interval = 7.60–15.48 mm) a clear tendency to isometry in most body segments was observed, suggesting that growth priorities have been fulfilled and the larvae will initiate with the transformation into a juvenile. These results provide a framework of the larval growth of L. peru in culture conditions which can be useful for comparative studies with other species or in aquaculture to evaluate the changes in larval growth due to new conditions or feeding protocols.     

Growth and morphological development of laboratory-reared larvae and juveniles of the Laotioan indigenous cyprinid Hypsibarbus malcolmi

The morphological development, including the pigmentation, body proportions, fins, and survival rate for 30 days after hatching, of laboratory-reared larval and juvenile Hypsibarbus malcolmi is described. Body lengths (BL) of larvae and juveniles were 2.0 ± 0.2 (mean ± SD) mm at 1 h after hatching (day 0) and 9.2 ± 0.6 mm on day 16, reaching 12.1 ± 0.9 mm on day 30. Yolk volume decreased linearly, with the yolk being completely absorbed by day 3 in all preflexion larvae (all specimens >3.2 mm BL). Feeding was observed on day 2 in fish which had rapidly undergone complete yolk absorption following mouth and anus opening on day 1, and on day 3 in all remaining fish. Myomere numbers were 20–21 + 11–12 = 31–33, although they were not clearly visible in juveniles. Melanophores were few on the body during days 0–2, but increased with growth and covered the entire upper dorsal body surface during the juvenile stage. Body proportions tended to become constant in juveniles. Notochord flexion began in larvae >5.2 mm BL on day 8, and was completed in larvae >8.4 mm BL on day 14. Specimens with full fin ray complements were initially observed on day 22 (10.4 mm BL in juveniles). All specimens >11.5 mm BL had attained the juvenile stage. A high survival rate of 92.7% was estimated on day 30.     

Growth and morphological development of laboratory-reared larval and juvenile Pangasianodon hypophthalmus

The morphological development, including the fins, body proportions and pigmentation, of laboratory-reared larval and juvenile Pangasianodon hypophthalmus was described and their behavioral features were observed under rearing conditions. Body lengths (BL) of larvae and juveniles were 3.0 ± 0.2 (mean ± SD) mm just after hatching, and 12.9 ± 1.1 mm on day 13, reaching 23.4 ± 1.8 mm on day 25 after hatching. Aggregate fin ray numbers (for caudal fin, principal soft ray number) attained their full complements in specimens larger than 12.8 mm BL. Notochord flexion began in yolksac larvae on day 0 (10.5 h after hatching), with teeth buds and barbels appearing with jaw formation in yolksac flexion larvae on day 1. Melanophores on the body increased with growth, with a broad vertical band forming on the lateral line and an oblique band extending from above the pectoral fin base towards the forepart of the anal fin during the postflexion larval and juvenile stages. Body proportions became relatively constant in juveniles, except for maxillary barbel length (MBL), which continued to decrease. Yolksac flexion larvae started feeding on day 2 with the onset of intense cannibalism. Yolks were completely absorbed by day 3, and cannibalism ended by day 6. Subsequently, fish displayed a schooling behavior with growth, preferring relatively dark areas during the juvenile stage.     

Morphometry of the Stone Loach, Barbatula Barbatula: Do Mensural Characters Reflect the Species' Life History Thresholds?

Growth variability in 23 mensural characters was examined in 387 specimens of stone loach, Barbatula barbatula, from England. The standard length (SL) of the specimens ranged from 15.3 to 115.4 mm. We tested the hypothesis that body proportions change abruptly, rather than gradually, at certain intervals of ontogeny by fitting linear, quadratic and split linear curves to plots of each variable against SL. Based on patterns of allometric growth, two groups and two subgroups of mensural characters have been found. Three characters were best explained by a linear regression, indicating isometric growth. Eight characters were best explained by a quadratic curve, indicating gradual allometry. The remaining 12 characters were best explained by a split regression, indicating mainly isometric growth with abrupt allometry occurring at a specific SL (breakpoint). The first shift in morphometric values (a transformation of the head; breakpoints in three characters) occurred at 26-35 mm SL, the second (a change in fin shape and size as well as body form; breakpoints in six characters) at 36-47 mm SL. The coincidence of shifts in body morphology with those in microhabitat use (between the respective size classes) suggests that thresholds (though not as sudden as those between embryo and early larva steps) do occur during this interval of stone loach life history. We suggest that the larva period ends with the completion of the first shift in relative growth (i.e. not later than at 35 mm SL, depending on individual variability), and that the second shift in morphometric values reflects a threshold between the first and the second step of juvenile period. The importance of changes in external morphology decreased as the fish grew bigger and older.     

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.     

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.     

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.     

Larval development of bigmouth manefish Caristius macropus (Perciformes: Caristiidae) from the western North Pacific

Larvae of bigmouth manefish Caristius macropus are described and illustrated on the basis of seven specimens (4.2–10.5 mm in body length) from the Kuroshio waters (0–60 m depth) and the transition waters (surface) between the Kuroshio and Oyashio fronts of the western North Pacific. The present larvae of C. macropus are distinguished from those of Paracaristius maderensis that inhabit the North Pacific by having 39–40 myomeres, 34 dorsal-fin rays, and 22 anal-fin rays. The present study, along with previous studies of the early life stages of caristiids, shows that larvae of the family may be defined by the following characters: body elongate in preflexion stage but becoming deep bodied and hatchet shaped after notochord flexion; anus located near vertical through base of pectoral fin; head large, without spination or serration; a distinct vertical band on the posterior tail throughout the larval stages, and two bands gradually appearing on the tail and trunk during the flexion and postflexion stages; and melanophores present around the notochord tip by the flexion stage. Adult C. macropus are found in the subarctic and temperate waters of the North Pacific; however, the present study and other occurrences of early life stages of the species probably indicate that C. macropus may spawn over a wide area in the North Pacific.