Swim bladder and posterior lateral line nerve of the nurseryfish, Kurtus gulliveri (Perciformes: Kurtidae)

The morphology of the swim bladder and inner ear of the nurseryfish, Kurtus gulliveri, appear adapted for enhanced pressure wave reception. The saccule is enlarged and surrounded by very thin bone and two large fontanelles that would present reduced resistance to pressure waves. The swim bladder is elaborate, with six dorsolaterally projecting pairs of lobes that are tightly encased in ribs and an additional caudally projecting pair of lobes encased in the first hemal spine. The ribs and musculature surrounding the swim bladder laterally are very thin, so that four or five "rib windows" are readily apparent on back-lit specimens. This swim bladder-rib configuration would also present reduced resistance to pressure waves to enhance function as a peripheral auditory structure. However, high-resolution X-ray computed tomography and dissection reveal no anterior projections of the swim bladder that could serve as a mechanical coupling to the inner ear. The posterior lateral line nerve is well developed and lies directly over the tips of the ribs encasing the swim bladder lobes. This nerve is not, however, associated with a lateral line canal and a lateral line canal is absent on most of the body. We hypothesize that the posterior lateral line nerve transmits mechanosensory information from the swim bladder.     

Temporal and spatial variation in potential and realized growth rates of age‐0 year northern rock sole

The possibility of prey limitations on the growth performance of age‐0 year northern rock sole Lepidopsetta polyxystra was evaluated at three sites along the north‐east coast of Kodiak Island, Alaska, U.S.A., by comparison of observed to potential growth rates. Growth potential was measured in the laboratory across the range of temperatures encountered by this species during the first summer of life. Growth potential ( g _L, mm day⁻¹) increased with water temperature (T) between 2 and 13° C, according to: g _L = 0·0151 + 0·3673·log₁₀(T). There were significant differences in growth rate between the three field sites such that Holiday Beach fish were 7·1 mm longer than Shakmanof Beach fish by mid‐September, with Pillar Creek Cove fish of intermediate size. Temperature differences between sites accounted for less than half of this variation. The remainder may have been related to differences in prey availability among the sites in association with observed differences in sediment characteristics. In addition to the spatial variability, there was significant monthly variation in growth performance. Realized growth rates between July and August were in excess of 85% of potential. Between August and September, however, realized growth fell to 43–71% of potential indicating a decline in conditions for growth. The spatial variation in growth rates was not density‐dependent as the site with the highest fish densities (Holiday Beach) also supported the highest growth rates. The available data indicates that for this subtidal species, interannual variation in growth may be more important than site variation.     

Age validation and growth of three commercially important hemiramphids in south-eastern Australia

The method of using sectioned otoliths to estimate age in three species of garfishes (family Hemiramphidae) was validated by: (1) staining fishes with the vital stain alizarin complexone (ALC) and periodically examining their otolith growth, and (2) marginal increment analyses. Staining fishes with ALC indicated that opaque zones were formed during winter and spring, but did not become visible on the otolith edge until late spring and summer. Hyporhamphus australis were found to be similar to the hemiramphids of the Atlantic in having fast growth rates and a maximum observed age of 4+ years old. Hyporhamphus regularis ardelio and Arrhamphus sclerolepis krefftii were found to be more similar to the southern sea garfish, Hyporhamphus melanochir , in being moderately long-lived, with maximum observed ages of 7+ years old for both species. Females grew faster and attained greater fork lengths than males for each species. Sectioned otoliths showed large variation in the appearance of opaque zones between the three species studied, with those from the wide-ranging, oceanic H. australis appearing inconsistent and diffuse when compared to the estuarine H. r. ardelio and A. s . krefftii . This variation was also apparent from fishes kept in aquaria, suggesting that the appearance of opaque zones in otoliths of these species is largely influenced by physiology, rather than by environmental conditions.     

Otolith and somatic growth rates in Atlantic salmon parr, Salmo salar L: evidence against coupling

It is often assumed that otolith growth is in some way dependent on somatic growth (i.e. that the two processes are coupled). We examined the relationships between sagitta radius and fork length in 0+ Atlantic salmon parr that would subsequently smolt aged 1 + (UMG fish) or 2+ (LMG fish). Repeated measurements of fork lengths of individually marked parr, taken over a 211-day period from first feeding, were compared to sagitta radii on the same measuring dates (obtained by analysis of daily increments). The results showed that there was a linear relationship between fork length and otolith radius in UMG parr. However, this was not true for LMG parr. These fish enter a state of natural anorexia in their first autumn (despite excess food), but their otoliths continued to grow at the same rate despite the virtual cessation of somatic growth; they had therefore developed disproportionately large otoliths by the end of the study period. The relative growth rates of soma and otoliths first changed in LMG fish in late July/early August; this is the most precise estimate yet obtained of the timing of divergence in the developmental pathways of UMG and LMG parr. The rate of sagitta accretion was consistently lower in LMG parr, possibly indicating a lower metabolic rate in these fish. The results are discussed in relation to previous theories of the relationship between otolith and somatic growth.     

Otolith increment widths and somatic growth rate: the presence of a time-lag

Populations of the estuarine glass fish, Ambassis vachelli Richardson, were used to study the relationship between somatic growth and widths of daily increments in the sagittal otoliths. Variations in the somatic growth of A. vachelli were induced by a series of experimental feeding regimes which included feeding to satiation with two food sources and a starvation treatment. After 33 days of exposure to the experimental feeding regimes significant differences in the mean wet weight of individuals amongst the feeding treatments were recorded. Fishes subject to a starvation treatment showed a significant reduction in wet weight compared to the pretreatment population and the two experimental feeding regimes. No changes in lengths of fishes were recorded.
Validation techniques revealed that daily increments were laid down in the sagittal and asteriscal otoliths. Estimates of ring widths from samples of sagittal otoliths revealed significant treatment effects. The increments of fishes from the starvation treatment showed a significant decline in mean increment width relative to the feeding treatments. This difference was detected only after a 15 day period of experimental feeding. It is suggested that the gradual decline in increment width reflects the exhaustion of readily mobilized energy reserves.     

Preparing sagittae for examination of daily growth increments of young‐of‐the‐year fishes: a modification of the embed method

A modification (termed the slide‐glass‐embed‐method, SGEM) of the embed method for preparing fish sagittae is described. The SGEM is based on a very simple principle: a dome of mixed resin containing the embedded sagittae loses hardness after being heated and can be easily cut with dissecting scissors.     

Comparison of otolith growth and morphology with somatic growth and age in young-of-the-year bluefin tuna

Otolith morphological characteristics were studied using image analysis techniques and the relationships between otolith growth and somatic growth and age, as estimated from counting daily otolith increments, were examined in young-of-the-year (YOY) bluefin tuna Thunnus thynnus ranging in fork length ( L _F) from 8·5 to 55·5 cm. Whole otolith length, width, area and perimeter, and three shape indexes, circularity, E value and rectangularity, were extracted for each pair of sagittae. Since no statistical significant differences between left and right otolith morphometrics were found, only one otolith from each fish was used for correlations. Statistically significant relationships were observed between otoliths measurements and fish somatic growth when a linear regression was applied after logarithmic transformation of all variables tested. Among the variables, otolith length was the one that showed the highest correlation with L _F, followed by otolith area and perimeter, whereas otolith rectangularity exhibited the lowest correlation. Statistically significant relationships were also observed between the otolith variables tested and the age of the fish, which ranged from 20 to 129 days. The ages estimated using otolith mass were very close to those assessed using daily increment counts (bias ranged from 1 to 24 days). Therefore, otolith mass could represent a valuable criterion for age estimation in YOY bluefin tuna that is objective, economic and easy to perform compared to daily increment counting method.     

Otolith microstructure and daily age of Anguilla japonica, Temminck & Schlegel elvers from the estuaries of Taiwan with reference to unit stock and larval migration

To test the hypothesis that the Japanese eel, Anguillu japonica , elvers in the eastern and western coasts of Taiwan are recruited from two different spawning grounds and to increase the knowledge of the early life history of the eel, the otolith microstructure and daily age of elvers collected from five estuaries in the coast of Taiwan during December 1989 through February 1990 were examined by scanning electron microscopy. The total length of elvers at arrival in the estuaries was similar among estuaries, averaging c . 56.0 mm and showed a seasonal decrease. The maximum radius of the sagittal otolith of elvers ranged from 124.46 to 181.82μm with a mean of 143.15 ± 12.72 μm. The otolith from centre to edge included an organic-rich primordium (9.20 ± 2.02 μm in diameter), a diffusively calcified core (20.94 ± 1.99 μm), and the daily growth increments; these three layers were probably deposited during the embryonic, yolk sac and feeding period respectively. The growth rate of the otolith was higher at the beginning of early life (0.5−1.0 μm day ⁻¹), lowest at approximately 100-days old (<0.5 μm day⁻¹), and highest 1 month before arrival at the estuary (> 1.0 pm day⁻¹). The mean age for elvers arriving in the estuaries of the coasts of Taiwan was approximately 170.4 ± 21.02 days. Neither the growth pattern of the otolith nor the age of elvers arriving in the estuary were significantly different among estuaries, indicating that the elvers in both eastern and western Taiwan were probably recruited from the same spawning ground. The growth pattern of the otolith in relation to larval migration was analysed.     

Age and growth of albacore Thunnus alalunga in the North Pacific Ocean

The age and growth of North Pacific albacore Thunnus alalunga were investigated using obliquely sectioned sagittal otoliths from samples of 126 females and 148 males. Otolith edge analysis indicated that the identified annulus in a sagittal otolith is primarily formed during the period from September to February. The assessments of the fish age at first annulus formation indicated that the first annulus represents an age of <1 year. This study presents an age estimate (0·75 years) for the formation of the first annulus. The oldest fish ages observed in this study were 10 years for females and 14 years for males. The von Bertalanffy growth parameters of females estimated were L(∞) = 103·5 cm in fork length (L(F) ), K = 0·340 year(-1) and t(0) = -0·53 years, and the parameters of males were L(∞) = 114·0 cm, K = 0·253 year(-1) and t(0) = -1·01 years. Sexual size dimorphism between males and females seemed to occur after reaching sexual maturity. The coefficients of the power function for expressing the L(F) -mass relationship obtained from sex-pooled data were a = 2·964 × 10(-5) and b = 2·928.     

Individual‐level analysis of pre‐ and post first‐feed growth and development in Atlantic salmon

Atlantic salmon Salmo salar were followed from egg to smoltification using genetic analysis to identify individuals and to link observations from pre‐ and post first feeding. Egg size and hatch timing significantly influenced alevin size at first feed but neither egg size, hatch timing or alevin sizes were correlated to size, condition factor or smolt status post first feed. In a hatchery environment the potential advantage gained by early hatching, larger alevin does not persist after first feeding. Different physiological and genetic complexes appear to influence growth in these two distinct phases of the Atlantic salmon's life‐cycle.     

Variability in growth of longfinned eels among coastal catchments of south‐eastern Australia

Longfinned eels Anguilla reinhardtii were captured by both fishery‐dependent and independent sampling methods from three rivers in New South Wales, south‐eastern Australia. Growth rates were examined in two zones (fresh water and tidal) in the Hacking, Hawkesbury and Clarence Rivers. Mean annual growth increments of sampled longfinned eels ranged from 30 to 60 mm year⁻¹ using age‐length analyses and up to 167 mm year⁻¹ based on tag‐recapture model estimates (GROTAG), with both methods showing high intra‐ and inter‐population variability. Growth was significantly faster in younger (5–15 years) fish than older (>15 years) fish, with females growing an average 10 mm year⁻¹ faster than males of similar age and capture location. Longfinned eels found in tidal areas grew significantly faster than those in non‐tidal freshwater areas as a result of longer growing seasons in the highly productive estuarine habitats. Other possible factors influencing variability in growth rates for this species include habitat preference, density and fishing pressure.     

Age and growth of the dusky grouper Epinephelus marginatus (Lowe 1834) in an exploited population of the western Mediterranean Sea

The age and growth of the dusky grouper, Epinephelus marginatus , in the Balearic Islands (western Mediterranean) were studied by otolith analysis from a sample of 358 specimens ranging in total length ( L _T) from 6·6 to 105·6 cm. The specimens came from commercial artisanal and recreational spear fisheries between 1999 and 2003. Otoliths grew asymmetrically throughout the range of L _T studied, showing a clear pattern of alternating translucent and opaque bands. Marginal increment analysis of specimens up to 8 years-old indicated that a single opaque band was formed each year during spring and summer. Whole otoliths allowed ageing specimens up to 10 years old, but above that age whole otoliths yielded lower age estimates than sectioned otoliths. The maximum estimated age was 61 years, which significantly extends the estimated life span of the species from a maximum of 36 years in a previous study. The von Bertalanffy growth parameters were estimated as L _∞= 95·5 cm L _T, K = 0·087 and T _O=−1·12. The study revealed differences in mean L _T at age and age structure between the shallow- and deep-water samples which may be attributed to different fishing pressure and environmental conditions.     

Age structure and growth of Semotilus atromaculatus(Mitchill) in PCB‐contaminated streams

Creek chub Semotilus atromaculatus from two PCB contaminated streams (Clear Creek and Richland Creek) at three locations and a reference stream (Little Indian Creek), Indiana, U.S.A., were examined to determine if age class structure and growth variables were correlated with in‐situ PCB exposure. Approximately five to 15 fish were captured weekly during the spring spawning season and monthly thereafter for a 12 month period. Fish collected ranged from 25 to 267 mm total length (L_T). Throughout the course of this study, no spawning activity was observed at either location in Clear Creek, although some very small young‐of‐the‐year (YOY) creek chub fry were observed at the downstream location by late summer. Creek chub nests were observed in both Richland Creek and Little Indian Creek but YOY were common only in Little Indian Creek. Exposure to PCBs was shown to both enhance and decrease growth in varied laboratory tests; subtle but significant gender‐specific differences in the growth of creek chub populations between the sites were observed. Creek chub up to 24 months in age from Clear Creek and Richland Creek were significantly larger (both L_T and mass for males and L_T for females) than reference site creek chub. This trend was reversed for creek chub aged ≥24 months as the reference site fish were consistently larger with reference males weighing significantly more. Older age classes of creek chub were missing in areas of higher PCB contamination. Female population growth rates and individual instantaneous growth rates were consistently higher at the reference site in comparison to the PCB‐contaminated sites. Calculation of ‘functional b’(as a condition factor) did indicate that growth enhancement in young males did occur at the most contaminated site and reductions in growth (mass relative to L_T) occurred in females from all contaminated sites. Furthermore, long‐term survivorship for females was reduced in the PCB‐contaminated streams. All of these subtle alterations in growth would not have been observed if males and females had not been analysed separately.     

Marbled lungfish growth rates in Lake Baringo, Kenya, estimated by mark‐recapture

Mark‐recapture was used to quantify the relationship between body mass ( M _T) and individual growth rates of sub‐adult marbled lungfish Protopterus aethiopicus in Lake Baringo, Kenya. Specific growth rate (in mass) was found to be a well defined and decreasing function of M _T over the size range of recaptured fish. Growth trajectories based on this function indicated that Lake Baringo African lungfish reached maturity at an age of c . 3 years and had a low reproductive effort.     

The effect of temperature and somatic growth on otolith growth: the discrepancy between two clupeid species from a similar environment

Otolith growth rates of the early life stages of herring Clupea harengus ( n = 472) and smelt Osmerus eperlanus ( n = 348) collected in the Vistula Lagoon (Baltic Sea) during 1997–1999 were analysed. The larvae and early juveniles were not only collected in the same geographical area they were also of the same size (range 15–43 mm standard length, L _S), similar ages and were collected during the same seasons (May to July). Although the two clupeid species experienced very similar environmental conditions, there were significant discrepancies in the analysed relationships. The otolith growth of larval and juvenile smelt was very strongly related to somatic growth while temperature had a minor effect. In herring, the effect of somatic growth, although clearly visible and statistically highly significant, was of less importance than temperature. Furthermore, variation in the otolith size and L _S relationship was affected by temperature and somatic growth in both species, but the variance of otolith size at L _S was higher for herring than for smelt. Although growth backcalculation from otoliths can presently be recommended as an appropriate method for use with both smelt and herring (despite possibly lower precision and accuracy with the latter), other methods referring directly to short-term increment width changes ( e.g. marginal increment analysis) are recommended for smelt but not for herring.     

Sex-specific somatic–otolith growth relationship in two Gadidae

Otolith and somatic mass of two Gadidae ( Merlangius merlangus and Trisopterus minutus ) were compared in order to analyse the sex-specific relationship between otolith and somatic growth at age. In the present study, otolith mass appeared a reliable indicator of age in both species. Otolith growth reflected somatic growth, but the relationship between these characters varied and differed between species and sexes.     

Inter‐individual differences in rates of routine energy loss and growth in young‐of‐the‐year juvenile Atlantic cod

Inter‐individual differences in rates of routine (non‐feeding) metabolism and growth were evaluated in young‐of‐the‐year (YOY) juvenile Atlantic cod Gadus morhua . Rates of O₂ consumption, CO₂ production and ammonia (TAN) excretion were measured in 64, 25–43 mm standard length ( L _S) YOY growing at different rates (0·27–0·47 mm day⁻¹) in a common rearing tank. Parameter rates ( y ) increased allometrically ( y = a·M^b ) with increasing body mass ( M ) with b ‐values for O₂ production, CO₂ consumption and TAN excretion equal to 0·81, 0·89 and 0·56, respectively. In some cases, residuals from these regressions were significantly negatively correlated to fish growth rate. In no cases did residuals of parameter rates increase with increasing growth rate. These data suggest that, during unfed periods, relatively fast‐growing fish were more metabolically efficient than slower‐growing fish from the same cohort. The fish condition factor, derived from     , also significantly decreased with increasing growth rate. Results indicated differences in both the rates of routine energy loss and the patterns of growth allocation among YOY Atlantic cod. Since these physiological attributes were positively correlated with growth rate, they may be indicative of 'survivors' in field populations.     

Age and growth of Saurenchelys (Nettastomatidae) and Dysomma (Synaphobranchidae) leptocephali in the East China Sea

The otolith microstructures of the leptocephali of Saurenchelys stylura and Dysomma sp., collected in November and December 2000 in the East China Sea, were examined to determine their larval ages and growth rates, and the spawning times of these two species of outer shelf and slope marine eels. Leptocephali ranging in size from 8 to 48 mm total length were examined, and the nettastomatid, S. stylura , and the synaphobranchid, Dysomma sp., had estimated ages that ranged from 16 to 75 days and 17 to 66 days, respectively. The overall growth rate of S. stylura was 0·68 mm day⁻¹( n  = 21), and of Dysomma sp. was 0·44 mm day⁻¹( n  = 22). These growth rates were similar or slightly faster than those observed for anguillid leptocephali in offshore areas of the western Pacific. The backcalculated hatching dates for these two species were from September to November. The otolith increment widths of S. stylura showed an increase before 20 to 30 days that were similar to those in anguillid species, but in Dysomma sp. there were no remarkable increases.     

Differences in size and growth rates of male and female migrating Japanese eels in Pearl River, China

The Sr/Ca ratios in otoliths of silver Japanese eels Anguilla japonica , in Pearl River, China, indicated that both sexes did not stay in brackish water and grew in fresh water from the glass eel stage until spawning migration. This did not support the hypothesis that females tended to distribute upstream and males might be restricted to estuaries. The back-calculated total length of males at glass eel stage was not significantly different from that of females, indicating that the hypothesis that small glass eels became males and larger ones became females may not be true. The mean (±S.D.) age and total length of males at migration were 6·4±1·6 years and 48·3±4·5 cm, which were significantly smaller than for females, 8·3±1·6 years and 61·4±4·1 cm. The age of migration was related inversely to growth rate for both sexes. Growth parameters of the von Bertalanffy growth equation were K =0·21 cm year°1, L _∞=55·7 cm and t _o=-0·55 year for males and K =0·14 cm year⁻¹, L _∞=77·5 cm and t _o=-0·60 year for females. The difference in asymptotic length ( L _∞) between males and females may be because females postpone migration to achieve larger size for maximizing reproductive success.     

Life‐history traits of the leatherjacket Meuschenia scaber,a long‐lived monacanthid

The present study describes the age and growth of the leatherjacket Meuschenia scaber, a common Australasian monacanthid and valued by‐catch of the inshore bottom trawl fishery in New Zealand. Age was determined from the sagittal otoliths of 651 individuals collected between July 2014 and March 2016 in the Hauraki Gulf of New Zealand. Otolith sections revealed alternating opaque and translucent zones and edge‐type analysis demonstrated that these are deposited annually. Meuschenia scaber displayed rapid initial growth, with both males and females reaching maturity in 1–2 years and 50% of both sexes matured at 1·5 years. Maximum age differed substantially between the sexes, at 9·8 years for males and 17·1 years for females. Growth rate was similar between sexes, although males reached greater mass at age than females in the early part of the lifespan. The length–mass relationship differed significantly between the sexes, with males displaying negative allometric growth and females isometric growth. Female condition was highest in July, declined in August with the onset of spawning and showed a slight peak in January and February, immediately following the spawning season. This study substantially extends the maximum longevity recorded for monacanthids, although males had much shorter lifespans and higher mortality, than females.