Oreoglanis infulatus, a new species of glyptosternine catfish (Siluriformes: Sisoridae) from central Vietnam

A new species of glyptosternine catfish, Oreoglanis infulatus , is described from the Lam River drainage in central Vietnam. The new species is distinguished from all its congeners by possessing the following combination of characters: a dark band running across the anal fin, a lunate and uniformly dark caudal fin, the lower lip lacking a medial notch and with a lobulate posterior margin, maxillary barbel with a rounded tip, length of caudal peduncle 19·0–22·6 % L _S, depth of caudal peduncle 2·6–3·2 % L _S, post-adipose distance 6·8–8·0 % L _S, eye diameter 10·5–12·1 % L _H, 12 principal caudal-fin rays.     

Larval development of five species of blenny (Teleostei: Blenniidae) from the western central North Atlantic, with a synopsis of blennioid family characters

Light trap collections on oil and gas platforms in the northern Gulf of Mexico off Louisiana from 1995 to 1997 contained young of tessellated blenny Hypsoblennius invemar , freckled blenny Hypsoblennius ionthas , featherduster blenny Hypleurochilus multifilis , molly miller Scartella cristata and seaweed blenny Parablennius marmoreus , which are described. Interspecific differences were: number of dorsal, anal, pelvic and caudal fin elements; number of mandibular pores; presence or absence of canine teeth, hypural 5 and pectoral fin pigment; width of gill openings; length of preopercular spines (in larvae). Size at settlement differed among some taxa, but all five species settled within a narrow size window of c . 1·5 mm standard length ( L _S). Hypsoblennius invemar , H. ionthas , H. multifilis and S. cristata settled at mean sizes between 11·3 and 12·1 mm L _S, whereas P. marmoreus settled at a mean size of 19·3 mm L _S. Sexually dimorphic differences were consistently evident by 17–18 mm L _S in all species but P. marmoreus . The two smallest blennies with external characters normally associated with sexual maturity were a 20 mm male and 21 mm female H. multifilis . Primary caudal fin rays began to bifurcate between 17·0 and 18·3 mm L _S in H. invemar , H. ionthas , H. multifilis and S. cristata . Hypleurochilus multifilis displayed the external characteristics of being sexually mature at 20–21 mm L _S. Thus, bifurcation of primary caudal fin rays was an indicator of approaching sexual maturity in H. multifilis and this may also be true in the other species studied.     

Development of the pectoral, pelvic, dorsal and anal fins in cultured sea bream

The pectoral fin girdle was the first element of the fins to develop in Sparus aurata. By 3·1mm L _N (notochord length) the cleithrum was ossified and the cartilaginous caracoid-scapula was present. The fin was fully developed at 11·6 mm L _S (standard length) and by 16·0 mm L _S most elements of the fin were ossified. The pelvic fins were the last pair to develop and rudiments of these were first detected at 7·9 mm L _S. The pelvic fin and girdle were completely formed and ossified at 16·0 mm L _S. The development of dorsal and anal fins began at c. 6·5–7·0 mm L _S with the formation of 10 cartilaginous dorsal proximal radials and eight cartilaginous ventral proximal radials. The three cartilaginous predorsals (supraneurals) appeared at 7·7 mm L _S and the ossification of dorsal and anal proximal and distal radials began, respectively, at 10·5 mm L _S and 11·3 mm L _S. Ossified structures in the fins were also classified according to their origin, as being either dermal or endochondral. Finally the chronology of appearance of fin structures in S. aurata was compared with that reported for other Sparidae, Engraulidae and Haemulidae.     

Seasonal variations in the energy density of fishes in the North Sea

The energy density ( E _D, kJ g^-1 wet mass) of saithe Pollachius virens , haddock Melanogrammus aeglefinus , whiting Merlangius merlangus , Norway pout Trisopterus esmarki , herring Clupea harengus , sprat Sprattus sprattus , sandeel Ammodytes marinus and pearlsides Maurolicus Muelleri , from the North Sea, increased with total length, L _T. However, there was not always a significant ( P> 0·05) linear relationship between L _T and E _D. Seasonal differences in E _D were obvious in mature fish, while geographical differences were insignificant. For all species there was a highly significant correlation ( P< 0·0001) between the percent dry mass of the fish ( D S) and E _D. A general relationship was established for gadoids and sandeel E _D=–3·1492+0·3459 D _S and herring E _D=–4·6395+0·4170 D _S. Thus seasonal and size-specific data on E _D needed for bioenergetics and gastric evacuation models can be determined simply from D _S, which is considerably less costly and time consuming than calorimetry or proximate analysis.     

Effect of body size on the standard metabolism of horse mackerel

The routine metabolic rate R _R and standard metabolic rate R _S were measured in horse mackerel Trachurus trachurus at 13°C over weight range of 1·4–390 g. A data extraction method rather than the more commonly used method of extrapolating the swimming speed-metabolic rate curves back to zero swimming speed was developed to measure the R _S. The relation between R _R and R _S and weight was expressed as a linear regression with the log transformed data. The mean slope of the regression was 0·752 for R _S and 0·725 for R _S.     

Morphological development and allometric growth patterns in the juvenile seahorse Hippocampus kuda Bleeker

The morphological development and allometric growth patterns in the juvenile spotted seahorse Hippocampus kuda were studied under hatchery rearing conditions. Newborn spotted seahorses [mean ± s.d . standard length ( L _S) 9·33 ± 0·79 mm] were raised till the age of 124 days (119·35 ± 6·04 mm). Growth was characterized by three stages with two inflexion points occurring at day 21 and 76. The mean growth rates in the first, second and third stages were 0·68, 1·16 and 0·71 mm day⁻¹, respectively. The growth rate was most rapid in the second stage and was probably influenced by a behavioural shift from pelagic to benthic form. The mass ( M ) and L _S relationship was exponential ( M = 7·14 × 10⁻⁶ L _S^2·76), but the slope, b = 2·76, reflected negative allometric growth. Sexes could be distinguished at c. 110 days, and the sex ratio was unbiased. The L _S in males and females did not differ significantly. Morphological stageing series is proposed, which divides H. kuda juvenile development into eight stages based on the development of coronet, cheek and eye spines, keel and pigmentation. The morphometric ratios for all the body parts, except trunk length, showed considerable changes at a transition point occurring at c. 25 mm L _S. The high proportional growth in head length, head depth, pectoral fin base length, dorsal fin base length, snout length, snout depth and eye diameter at the initial stages, and the abrupt increase in tail length only after the first 2 weeks, possibly reflect development priorities during early development where important organs are being developed first for the enhancement of juvenile survival.     

Shrinkage correction and length conversion equations for Theragra chalcogramma, Mallotus villosus and Thaleichthys pacificus

Preservation of walleye pollock Theragra chalcogramma, capelin Mallotus villosus and eulachon Thaleichthys pacificus by freezing decreased fork length ( L _F) up to 1·8, 5·6 and 2·7% and reduced mass by up to 8·4, 3·5 and 1·1%, respectively. Shrinkage of walleye pollock standard length ( L _S) was greater for fish in 95% ethanol v . 5% formalin and for fish in 10% formalin v . frozen. Equations describing the shrinkage and loss in mass for these species are presented as well as conversions between different length measurements ( L _S, L _F and total length, L _T) for fishes that were frozen.     

A new species of the scorpionfish genus Scorpaena (Scorpaenidae) from Izu Peninsula, Pacific coast of Japan

A new species of scorpionfish, Scorpaena brevispina , is described on the basis of a single specimen collected from off the east coast of Izu Peninsula, Pacific coast of Japan, at a depth of 45 m. Scorpaena brevispina is distinguished from other Indo–Pacific species of Scorpaena by the following combination of characters: pectoral-fin rays 17; longitudinal scale rows 44; scales below lateral line 13; gill rakers 17; anterior surface of preocular spine with three vertical or slightly oblique ridges; lateral surface of maxilla without a distinct longitudinal ridge; lateral lacrimal spine present; extremely deep occipital pit; occipital pit rectangular in dorsal view, length distinctly less than width (length 53·3% of width); numerous small papillae on surface of occipital pit; pectoral fin relatively long (33·3% of standard length, L _S), posterior tip extending beyond verticals through last dorsal-fin spine base and second anal-fin spine base; relatively short third to fifth dorsal-fin spines (third spine length 14·6% of L _S, fourth spine 15·5%, and fifth spine 15·8%, respectively).     

Effects of temperature, body size and feeding on rates of metabolism in young‐of‐the‐year haddock

The mean rate of oxygen consumption (routine respiration rate, R _R, mg O₂ fish⁻¹ h⁻¹), measured for individual or small groups of haddock Melanogrammus aeglefinus (3–12 cm standard length, L _S) maintained for 5 days within flow‐through respiratory chambers at four different temperatures, increased with increasing dry mass ( M _D). The relationship between R _R and M _D was allometric ( R _R = α  M ^b ) with b values of 0·631, 0·606, 0·655 and 0·650 at 5·0, 8·0, 12·0 and 15·0° C, respectively. The effect of temperature ( T ) and M _D on mean R _R was described by     indicating a Q ₁₀ of 2·27 between 5 and 15° C. Juvenile haddock routine metabolic scope, calculated as the ratio of the mean of highest and lowest deciles of R _R measured in each chamber, significantly decreased with temperature such that the routine scope at 15° C was half that at 5° C. The cost of feeding ( R _SDA) was c . 3% of consumed food energy, a value half that found for larger gadoid juveniles and adults.     

Seasonal differences in muscle fibre recruitment of pilchard larvae in the north‐western Mediterranean

The recruitment of slow and fast myotomal muscle fibres with respect to growth in body length in European pilchard larvae Sardina pilchardus [(3·5–13·5 mm standard length ( L _S)] was significantly higher in November 1998 than February 1999. This resulted in a significant seasonal difference in the relationship between fibre number and L _S, particularly for the fast muscle. Mean sea surface temperature was c . 6° C higher in November than February, whereas the mean abundance of potential prey items (copepod nauplii) was comparable between cruises. Laboratory and field data obtained from other clupeid species have indicated the importance of early thermal experience on muscle fibre recruitment patterns. Differences in average sea temperature therefore provide a plausible mechanism for the observed seasonal differences in muscle growth characteristics.     

The ontogeny of habitat associations in the tropical tiger tail seahorse Hippocampus comes Cantor, 1850

This study examined how habitat associations changed with ontogeny in the tiger tail seahorse Hippocampus comes Cantor, 1850, over four reef zones in a coral reef ecosystem. Hippocampus comes showed ontogenetic differences in their use of habitat at the scale of reef zones (macrohabitat) and holdfasts (microhabitat). Across reef zones, juvenile size classes (25–105 mm standard length, L _S) were most abundant in wild macroalgal beds ( Sargassum spp.) (55·7%), while adults (>105 mm L _S) occupied both coral reefs (39·7%) and macroalgal beds (42·7%). Microhabitat use also varied with ontogeny. Juveniles generally used macroalgal holdfasts, while adults >135 mm L _S used a greater diversity of specialized microhabitats that included branching sponges, branching corals and tall seagrass. Ontogenetic changes in habitat association, as well as size-related shifts in crypsis and aggregation, suggest that H. comes experiences fitness trade-offs that vary with size; juveniles may associate with habitat that reduces predation, while larger individuals may use distinct microhabitat in reef zones to optimize reproductive success. Results are discussed in the context of targeted exploitation, expanding artisanal mariculture, habitat damage from illegal fishing and reserve design.     

Effect of body size, temperature, and salinity on the routine metabolism of larval and juvenile spotted seatrout

Routine oxygen consumption rates of young spotted seatrout Cynoscion nebulosus (Sciaenidae) were measured over a range of temperatures (24, 28, 30 and 32° C) and salinities (5, 10, 20, 35 and 45). Larvae and juveniles, 4·1–39·5 mm standard length ( L _S), ranging several orders of magnitude in dry body mass were used to estimate the mass–metabolism relationship. Oxygen consumption (μl O₂ larva⁻¹ h⁻¹) scaled isometrically with body mass for larvae <5·8 mm L _S(phase I, slope = 1·04) and allometrically thereafter (phase II, slope = 0·78). The inflection in the mass–metabolism relationship coincided with the formation of the hypural plate and an increase in the relative tail size of larvae. Salinity did not have a significant effect on routine metabolism during phase I. Temperature and salinity significantly affected routine metabolism during phase II of the mass–metabolism relationship. The effect of salinity was temperature dependent, and was significant only at 30° C. Response surfaces describing the environmental influences on routine metabolism were developed to provide a bioenergetic basis for modelling environmental constraints on growth.     

Growth variation in larval Makaira nigricans

The Atlantic blue marlin Makaira nigricans larvae were collected from Exuma Sound, Bahamas and the Straits of Florida over three summers (2000–2002). Sagittal otoliths were extracted and read under light microscopy to determine relationships between standard length ( L _S) and age for larvae from each year and location. Otolith growth trajectories were significantly different between locations: after the first 5–6 days of life, larvae from Exuma Sound grew significantly faster than larvae from the Straits of Florida. Exponential regression coefficients were similar among years for Exuma Sound larvae (mean instantaneous growth rate, G _L = 0·125), but differed between years for larvae from the Straits of Florida ( G _L = 0·086–0·089). Differences in larval growth rates between locations resulted in a 4–6 mm difference in L _S by day 15 of larval life. These differences in growth appeared to be unrelated to mean ambient water temperatures, and may have been caused by location‐specific differences in prey composition or availability. Alternatively, population‐specific differences in maternal condition may have contributed to these differences in early larval growth.     

Ontogenic changes in the allometric scaling of the mass and length relationship in Sprattus sprattus

An analysis of mass ( M ) and standard length ( L _S) data for larval, juvenile and adult sprat ( Sprattus sprattus ; Clupeidae) revealed marked changes in the allometric scaling factor ( b in     ). For sprat <44 mm L _S, b was 5·0, whereas in larger juveniles and adults, b was c. 3·4 indicating a relatively protracted metamorphic period for this species.     

Reduced swimming abilities in fast-growing transgenic common carp Cyprinus carpio associated with their morphological variations

Critical swimming speeds ( U _crit) and morphological characters were compared between the F₄ generation of GH-transgenic common carp Cyprinus carpio and the non-transgenic controls. Transgenic fish displayed a mean absolute U _crit value 22·3% lower than the controls. Principal component analysis identified variations in body shape, with transgenic fish having significantly deeper head, longer caudal length of the dorsal region, longer standard length ( L _S) and shallower body and caudal region, and shorter caudal length of the ventral region. Swimming speeds were related to the combination of deeper body and caudal region, longer caudal length of the ventral region, shallower head depth, shorter caudal length of dorsal region and L _S. These findings suggest that morphological variations which are poorly suited to produce maximum thrust and minimum drag in GH-transgenic C. carpio may be responsible for their lower swimming abilities in comparison with non-transgenic controls.     

Effects of delayed first feeding on the nutritional condition and mortality of California halibut larvae

The effect of the timing of first feeding (3, 4, 5, 6, 7 and 8 days post‐hatch, dph) on laboratory‐reared California halibut Paralichthys californicus larvae was evaluated by means of morphologic, morphometric and histological criteria. Larvae began to feed exogenously at 3 dph (2·7 ± 0·01 mm standard length, L _S) at 18° C. Eye pigmentation, rather than mouth opening was the most distinctive trait of California halibut larvae at first feeding. Larval growth was significantly affected by the time of first exogenous feeding. At notochord flexion (21 dph), the L _S of larvae fed for the first time at 3 dph was significantly larger (5·1 ± 0·1 mm) than that of those fed at 4 and 5 dph (4·9 ± 0·1 mm), although the latter fish had a more uniform size distribution. The point of no return was reached at 7 dph. Survival of larvae initially fed at 3, 4 and 5 dph was similar (58·4–60%), while no larvae were able to survive when food was offered for the first time between 6 and 8 dph. Food deprivation resulted in a progressive deterioration of the larval digestive system and atrophy of skeletal muscle fibres. Significant changes in the anterior and posterior enterocyte height were detected after 2 days of food deprivation. Similarly, tail height: L _S and trunk length: L _S ratios were the most sensitive morphometric indices to detect the effect of fasting on larval condition. Present results show that a combination of morphometric and histological variables can be used to evaluate the nutritional condition of California halibut larvae.     

Growth of young-of-the-year mackerel in the Bay of Biscay

The first growth season of young-of-the-year (0+ year) mackerel Scomber scombrus , sampled in the Bay of Biscay, was parameterized to determine growth patterns. Daily increments were identified on sagittae otoliths, for calculation of age and growth of 92 larvae and 54 juveniles over the range 3·6–215·0 mm standard length ( L _S). A Gompertz curve was fitted to the length-at-age data. At the end of the first year of growth L _S was 194·2 mm, with a maximum growth increment of c . 2 mm day⁻¹, observed 62 days after hatching. Backcalculated growth increments for mackerel juveniles, during their larval stage, were higher than those observed for sampled larvae; only 10·9% of sampled larvae were estimated to survive. Growth for north-eastern Atlantic mackerel was slower than that published for north-western Atlantic mackerel. Backcalculated hatching dates for mackerel were consistent with the typical temporal distribution of mackerel spawning in the Bay of Biscay.     

Effects of temperature on prey consumption and growth in mass of juvenile trahira Hoplias aff. malabaricus (Bloch, 1794)

The influence of temperature on prey consumption and growth in mass of juvenile trahira Hoplias aff. malabaricus were investigated. Consumption of small-sized lambari Astyanax altiparanae (mean standard length, L _S, 5·43 cm) varied from zero to 65 over a period of 30 days. Temperatures ranged from 14 to 34° C and the size of trahiras ranged from 17·5 to 24·7 cm L _S. Prey consumption differed significantly among temperatures. Trahiras at 18° C consumed significantly less than those at 30° C. A linear multiple regression model including temperature, prey consumption and L _S explained 89·4% of the variability in growth in mass. Some caution is suggested when inferring the impact of H. aff. malabaricus piscivory on assemblage structures in systems that, despite their location in tropical regions, are subjected to seasonal thermal variations.     

Differences in temperature conditions and somatic growth rate of larval and early juvenile spring-spawned herring from the Vistula Lagoon, Baltic Sea manifested in the otolith to fish size relationship

Larval and juvenile herring Clupea harengus collected in the Polish part of the Vistula Lagoon in May-July 1997 had hatched between 17 April and 9 June and originated from three cohorts. The spawning season began on 1 March at 3·8° C and was completed on 3 June at 12·7° C. Mortality among larvae was high in the first 2 weeks of April, probably associated with significant temperature decrease at the beginning of the spawning season. The growth of 10–48 mm L _S herring was linear, highest for larvae and juveniles from the first cohort (0·58 mm mm^-1 day^-1), slower for the second cohort (0·55 mm mm^-1 day^-1) and the slowest for the third cohort (0·45 mm mm day^-1). Temperature effects on the growth were inconclusive and potentially unfavourable feeding conditions in June might have been responsible for the relatively slow growth of third cohort larvae and juveniles.
Relationships between otolith size (perimeter, length, width, area, and weight) and fish size ( L _S) differed among the three cohorts, related mostly to the positive temperature effect on otolith growth, individuals growing in warmer water had larger otoliths. Although a negative growth rate effect was observed as well, it was less significant.     

Larval Konosirus punctatus(Clupeidae) in a brackish river mouth on the Pacific coast of central Japan

Eggs of Konosirus punctatus in early developmental stages were collected from the eastern part of the mouth of Sagami Bay on the Pacific coast of central Japan. Advanced‐stage eggs and early larvae with notochord length ( L _N) of <7·5 mm were collected from the inner bay near the mouth of the Sagami River. Feeding larvae of >8·4 mm L _N were distributed in the mouth of the river, and juveniles of 24–90 mm standard length ( L _S) were collected from the lower reaches of the river between the river mouth and c . 3 km upstream of the river mouth. Hatch dates of larvae and juveniles collected in 2001 ( n  = 158) and in 2002 ( n  = 109) extended from late March to late July. The relationship between the otolith radius ( R _O) and L _N or L _S changed during the metamorphosis stage as characterized by 320 μm R _O and 22 mm L _S. Otolith growth rate, as an index of somatic growth rates in larval and early juvenile stages, was higher in cohorts that hatched later in the spawning season, i.e . from March to July. Konosirus punctatus that were spawned in the bay mouth area survived with different growth histories in the bay and lower reaches of the river, and recruited to the young‐of‐year population in the Pacific coastal waters of central Japan.