Discrepancies between otoliths of larvae and juveniles of the American eel: is something fishy happening at metamorphosis?

The use of otoliths to interpret early life history in fishes depends upon the assumptions that otoliths record past events accurately and consistently and that records of events in otoliths are continuous. Both the number of growth microincrements ( I ), and the radii ( R ,μm) of otoliths of American eel Anguilla rostrata , leptocephali increased linearly and highly significantly with leptocephalus body length ( L , mm), as expected on the above assumptions ( I , =2·29 L , − 5·75 and R , =1·05 L , + 12·02, r ²,=0·938 and 0·931, n , =20). In contrast, the number of increments and the radii of the leptocephalus growth zones of otoliths of glass-phase American eels were not related to body length, and they were lower than predicted by the relationships developed for leptocephali. Thus, otoliths of American eels apparently violate one or both assumptions. Possibly, the margin of the otolith is resorbed during metamorphosis from leptocephalus to glass eel, perhaps as part of calcium metabolism as skeletal elements are being formed.     

Validation of the periodicity of increment formation in the otoliths of a cichlid fish from Lake Tanganyika, East Africa

Tetracycline was used as a chemical tag in a mark‐recapture study to examine the pattern of increment formation in the otoliths of Tropheus moorii , a rock‐dwelling cichlid from Lake Tanganyika. A total of 256 fish were captured by divers and injected with tetracycline. Of these, nine were recaptured after either 1 or 2 years at liberty and eight retained tags within their otoliths. Comparison of the number of growth increments formed after the tag and the time at liberty demonstrated that increments were deposited on an annual basis in the otoliths of this species. Furthermore, there was a strong relationship between otolith mass and age suggesting that otoliths grew at a predictable rate throughout the life of the fish. Validation of an annual pattern of increment deposition allowed age and growth information to be derived from otoliths. This showed that T. moorii grew rapidly to attain adult size by 3 years of age. Males grew faster than females and also attained a larger size than females (8·74 v . 7·91 cm L _S respectively). The longevity of some of these small freshwater fish was surprising; the oldest individual had an age of 10 years, while the average age of adults was 4 years.     

Variation in the sex ratio, size and age of longfinned eels within and 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. Sex ratios, catch per unit effort and population age and total length structure were examined in three zones (fresh water and upper and lower tidal) in the Hacking, Hawkesbury and Clarence Rivers. Females were found in relatively high proportions in all zones, ranging from 97% in a freshwater (non‐tidal) site down to 59% in a tidal site. Males were found primarily in tidal zones (only two of the 677 longfinned eels caught in non‐tidal fresh water were males), with the greatest proportions being found in the brackish upper tidal areas. The mean number of fish captured per trap was higher in the fresh water and upper tidal zones than in the lower tidal zones. The mean ±  s . e . age, 17·9 ± 0·3 years, and age range, 5–52 years for females were significantly higher than those of males 12·2 ± 0·4 years; range 5–22 years, which is typical of other anguillid species. Longfinned eels captured in fresh water were found be significantly larger and older than those in tidal zones due to the almost exclusive predominance of females.     

Bathymetric distribution and growth patterns of Bathypterois mediterraneus from the north-western Mediterranean Sea

Bathypterois mediterraneus was collected on 148 bottom trawls between 147 and 2251 m depth in the north-western Mediterranean. The species appeared below 700 m, its relative abundance and biomass increased progressively and reached its maximum at 2100-2300 m. A total of 1913 specimens were measured, ranging from 4 to 20 cm standard length ( L _s). The size composition with depth did not show any specific trend, and no modal progression could be distinguished in the length frequency distribution by cruise, with dominance of large fish (13-15 cm L _s) and a unimodal size pattern. The otoliths of 173 specimens were examined and showed the ring pattern common to teleost fishes. The age ranged between 0 and 15 years, although specimens of 4-12 years old were the most abundant. The growth parameters and the growth curve obtained from the interpretation of the growth rings in otoliths showed a low growth rate.     

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.     

The role of food particle size in the growth of juvenile Atlantic salmon (Salmo salar L.)

The effect of particle size of a commercial pelleted feed on the growth of Atlantic salmon from first feeding alevins to first and second year smolts was investigated using 20-day feeding experiments. Ten experiments were performed over a two year period, each comprising six groups of fish separately selected from stock populations. Each group was presented with one of six sizes of food particle ranging from larger than the respective mean mouth breadth (100% feed size), through 50%, 25%, 12·5%, 6·25% to 3·125%. Experiments were performed in six radial flow/circumferential drain tanks under ambient photoperiod and water temperature. Growth rate was found to be closely related to feed size. Maximum growth in each case was shown only on one size of particle; larger and smaller sizes resulted in reduced growth. The particle size for maximum growth increased in direct proportion to fish length. Fish from 4·2 to 20·3 cm in length showed maximum growth on particle diameters 0·022 to 0·026 × fish fork length (PFR). First feeding alevins were found to show comparable growth rate on particle diameters 0·0115 to 0·090 PFR. Some seasonal variation in growth response was indicated. The results are discussed in relation to developmental and seasonal effects. Possible factors affecting the energetics of prey size related differential growth are discussed.     

A hydro-mechanical approach to the scaling of swimming performance in the sand flathead Platycephalus bassensis Cuvier: effects of changes in morphological features based on fish size

The swimming performance of Platycephalus bassensis at steady speed was assessed with an emphasis on hydrodynamics. The minimum swimming speed to maintain hydrostatic equilibrium for P. bassensis of 0·271 m total length ( L _T) was calculated to be 1·06 L _T s⁻¹. At this speed, the required lift to support the mass of the fish was equivalent to 6·6% of the fish mass; 82·7% of which was created by the body as a hydrofoil, and the rest of which was created by the pelvic fins as hydrofoils. The minimum swimming speed decreased with the L _T of the fish and ranged from 1·15 L _T s⁻¹ for a fish of 0·209 m to 0·89 L _T s⁻¹ for a fish of 0·407 m. The forward movement per tail-beat cycle ( i.e. stride length) was described with an equation including quantities of morphological and hydro-mechanical relevance. This equation explained that stride length was increased by the effect of turbulence characterized by the Reynolds number and demonstrated the morphological and hydro-mechanical functional design of the fish for maximizing thrust and minimizing drag. The larger span of the caudal fin and caudal tail-beat amplitude was associated with larger stride length, whereas greater frictional drag was associated with smaller stride length.     

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.     

Rapid data collection and assessment of the biology of Acanthurus nigrofuscus at Woleai Atoll, Micronesia

Traditional community fishing methods commonly employed in the tropical Pacific were used to generate information on the fishery biology of Acanthurus nigrofuscus at Woleai Atoll, Micronesia, over a short time period. A simple depletion model was used to estimate the biomass of A. nigrofuscus at four back reef lagoon sites at Woleai, using two different fishing methods; spear fishing and drive-in-net fishing. The mean biomass and density of A. nigrofuscus on the lagoon reefs was 8000 g ha ⁻¹ and 183 fish ha ⁻¹ respectively, with a total estimated standing stock for the lagoon of 91 500 fish or a biomass of 4·0 t. The size frequencies of fish caught by spear fishing were biased towards larger sized individuals, while those from drive-in-net fishing were thought to be more representative of the true population size frequencies. Variation in the density and biomass of A. nigrofuscus at the four reef sites was thought to be due to the length of time between episodes of community fishing at each reef site. The sex ratio (male: female) of A. nigrofuscus was significantly different from unity (1: 0·47) and males grew larger than females. Sexually mature fish were present in all size classes above the minimum capture length and spawning activity was greatest during the period of the full moon.     

On the life history of the lesser gurnard (Scorpaeniformes: Triglidae) inhabiting the Agulhas Bank, South Africa

Growth analysis based on sectioned sagittal otoliths revealed the lesser gurnard Chelidonichthys queketti on the Agulhas Bank to be relatively fast growing and long lived, with ages of up to 7 years being recorded. Total length at age (mm) was described best by the specialized von Bertalanffy growth model as L _T=306·1 (1 − e^{0·53(t+0·18)}). First approximations of total, natural and fishing mortality rates were determined at 0·73, 0·38 and 0·35 year⁻¹ respectively. The adult population was male dominated with a sex ratio of 1 female: 1·2 males with the mean size of males and females being similar. The lesser gurnard is an iteroparous species with females maturing by the end of the first year of life (195 mm L _T), thereafter spawning throughout the year with reproductive activity peaking over spring and late summer. The lesser gurnard appears to exhibit similar life-history patterns to other triglid species in that it can be classified as a generalist. Generalistic life-history characteristics such as a fast growth rate, early sexual maturity at a relatively large size, a non-seasonal spawning pattern, feeding on a variety of prey organisms and the ability to inhabit various substrata could all contribute to it maintaining a high biomass on the Agulhas Bank.     

Population genetic structure and effective population size of ayu (Plecoglossus altivelis), an amphidromous fish

The temporal and spatial population genetic structure of ayu Plecoglossus altivelis (Salmoniformes: Plecoglossidae), an amphidromous fish, was examined using analysis of variation at six microsatellite DNA loci. Intracohort genetic diversities, as measured by the number of alleles and heterozygosity, were similar among six cohorts (2001–2006) within a population (Nezugaseki River), with the mean number of alleles per cohort ranging from 11·0 to 12·5 and the expected heterozygosity ranging from 0·74 to 0·77. Intrapopulational genetic diversities were also similar across the three studied populations along the 50 km coast, with the mean number of alleles and the expected heterozygosity ranging from 11·33 to 11·67 and from 0·75 to 0·76, respectively. The authors observed only one significant difference in pair-wise population differentiation ( F _ST-value) between the cohorts within a population and among three populations. Estimates of the effective population size ( N _e) based on maximum-likelihood method yielded small values (ranging from 94·8 to 135·5), whereas census population size ranged from c. 4800 to 24 000. As a result, the ratio of annual effective population sizes to census population size ( N _e/ N ) ranged from 0·004 to 0·023. These estimates of N _e/ N agree more closely with estimates for marine fishes than that of the larger estimates for freshwater fishes. The present study suggests that ayu which is highly fecund and shows low survival during the early life stages is also characterized by having low value of N _e/ N , similar to marine species with a pelagic life cycle.     

Effects of confinement stress of variable duration on the growth and microincrement deposition in the otoliths of Oreochromis niloticus(Cichlidae)

The effects of chronic confinement stress (1, 5 and 10 days) and of periodic blood sampling on somatic growth and the structure and growth of otoliths was studied in Oreochromis niloticus . During the study, the plasma concentrations of cortisol were measured at various times during the application of stress: they were significantly higher in confined fish than in control fish (mean ±  s . d . 3·40 ± 0·47 v . 1·26 ± 0·62 ng ml⁻¹, P  < 0·05) up to 5 days after the start of a 10 day stress period. The somatic growth (standard length, L _S, and mass) was affected by the confinement and by the sampling (from 16·21 ± 1·07 to 14·64 ± 1·15 cm for L _S, and from 173·31 ± 33·14 to 110·50 ± 29·48 g for mass). But the confinement masked the effect of the sampling on somatic growth. Tetracycline was injected at the start of the experiment to mark the otoliths, and showed that the short and long duration confinements led to a clear check in the pattern of primary increments in the otoliths. The number of primary increments deposited during the resting periods that followed each period of confinement was always less than the number of days that these periods lasted. No relation was found between the duration of confinement and the structure of the resulting checks. These results suggest that there is a disruption in the laying down of primary increments during periods of confinement resulting in an underestimation of their number compared to the actual number of days of growth. These results call into question the use of otolith primary increments as a means of estimating the age of Nile tilapia that have experienced periods of stress.     

Relationships between fish size and otolith size of four bathydemersal fish species from the south eastern Arabian Sea,India

The objective of this study was to estimate a prey body size from the hard parts (e.g. otoliths) of a fish species frequently found in the guts of predators. Length–weight relationships between otolith size (length, height, weight and aspect ratio) and fish size (total length and weight) were determined for four fish species captured in the Arabian Sea by bottom trawl (2015 survey on‐board FORV Sagar Sampada, 200–300 m depth), off the west coast of India: Psenopsis cyanea, Pterygotrigla hemisticta, Bembrops caudimacula and Hoplostethus rubellopterus. No significant differences were noted between the size of the left and right otoliths (t test) in any of the four species. The length–weight relationship of the otolith in all four species showed a negative allometric growth pattern (t test, p < .05). The data fitted well to the regression model for otolith length (OL), otolith height (OH) and otolith weight (OW) to total length (TL) and total weight (TW). Results showed that these relationships are a helpful tool in predicting fish size from the otoliths and in calculating the biomass of these less‐studied fish species during feeding studies and palaentology.     

Growth and morphological development of sagittal otoliths of larval and early juvenile Trachurus japonicus

The daily periodicity of growth increment formation in sagittal otoliths of jack mackerel Trachurus japonicus was validated by marking otoliths with alizarin complexone (ALC). Analysis of otoliths of known‐age juveniles confirmed that the first increment formed on day 3 after hatching, and was associated with first feeding. A total of 198 specimens, ranging from 2·6 to 49·2 mm in body length (notochord length or standard length) and from 7 to 78 days in age, were collected in the East China Sea and Tosa Bay, and used to examine the association between otolith morphological development and ontogenetic development. The relationship between body length ( L ) and otolith radius ( R ) was significantly described by the linear function L  = 2·65 + 0·0425 R ( n  = 198, r ² = 0·99, P  < 0·001), indicating that somatic growth history can be reconstructed from otolith growth patterns. The otolith was primarily spherical in the preflexion larval stage, and became elongated with notochord flexion. The first secondary primordium formed at c . 25 days, during the middle postflexion stage, and was associated with metamorphosis. By c . 42 days the sagittal otolith was adult‐like in morphology, with the primary growth zone enclosed by the marginal growth zone, except in the anterior rostrum area. Thus age, growth and developmental stages were recorded in sagittal otoliths during the larval and early juvenile stages of jack mackerel.     

Distribution and reproduction of the southern lantern shark from New Zealand

Distribution, population structure and reproduction are described for the southern lantern shark Etmopterus granulosus at the Chatham Rise, New Zealand. Depth of capture for E. granulosus ranged from 744 to 1420 m, with highest catch rates between 800–1200 m. More than twice as many females as males were captured, and the majority of sharks caught were mature, indicating that there may be segregation according to sex and size class. Only 10 of 492 female sharks captured contained ova in uteri, and none contained embryos. The absence of pregnant females suggests that they move to another area or depth prior to pupping. Size of sharks captured ranged from 20·0 to 78·8 cm total length. Females began to mature at 62 cm total length, and males at 52 cm. There was no evidence of a seasonal reproductive cycle. Ovulation appeared to occur when ova reached a diameter of 40–45 mm. The average number of ova in mature females was 12·7. This information is crucial for assessing the impact of fisheries on E. granulosus populations.     

Depth distribution and biological characteristics of the European eel Anguilla anguilla in Lough Ennell, Ireland

Using a longline survey, a total of 196 European eels Anguilla anguilla were collected at different depths in Lough Ennell (maximum depth 30 m), central Ireland. The catch per unit of effort of A. anguilla that were caught from 1 to 25 m depths was lowest at 0·5–5·0 m and greatest at the deepest depth range (22·5–25·0 m). Sub-samples of A. anguilla from depths of <15 m showed little or no difference in size, sex ratio, age, growth rate, condition factor, length–mass relationship, gonado-somatic index, fin index or eye index with fish from depths of >15 m. All fish examined were female yellow-phase A. anguilla that had ages from 7 to 20 years (mean ± s . d . = 10·3 ± 2·9 years), with growth rates from 24·0–60·8 mm year⁻¹ (mean ± s . d . = 40·7 ± 8·5 mm year⁻¹). Variations in the growth rates were greater in the shallow group than that of the deep group. This study suggested that deeper regions are important feeding habitats for A. anguilla and that fish in this lake were growing moderately fast compared to similar habitats and areas in the species' range.     

Age estimation,growth and maturity of the Argentine hake (Merluccius hubbsi Marini, 1933) along the northernmost limit of its distribution in the south-western Atlantic

Age, growth and length-at-maturity of the Argentine hake (Merluccius hubbsi) were studied in the northernmost limit of the species distribution in the south-western Atlantic. A total of 351 otoliths and information from 1610 specimens sampled from the industrial double-rig trawl landings between May 2013 and April 2014 were used. Age and growth were estimated by counting and measuring increments in sectioned sagittae otoliths, and length at maturity was estimated based on macroscopic gonadal analysis. For both sexes, hepatosomatic index and condition index increased mainly during spring, reaching a maximum at the end of summer before the subsequent spawning season began. Gonadosomatic index was highest in April, believed to correspond with peak spawning. The annual periodicity of alternate opaque and translucent zones was validated by marginal increment analysis. Growth curves were fitted to back-calculated size at age by fitting the three-parameters von Bertalanffy growth function. The maximum age was 5 years in fish of either sex. Females attained larger sizes than males. The parameters of the von Bertalanffy growth equations were: L∞?=?533?mm, k?=?0.231 year^?1 and t₀?=??0.935 year for females; L∞?=?394?mm, k?=?0.405 year^?1 and t₀?=??0.463 year for males. The mean length and age at first maturity was 273?mm at 1.9 years for males and 274?mm at 2.0 years for females.     

Spring cannibalism on 1 year walleye pollock in the Doto area,northern Japan: is it density dependent?

Cannibalism in walleye pollock off the eastern coast of the Hokkaido Island, Japan was important only during spring (April to June), and its importance increased from 0% in dry mass for <200 mm L _S fish to 48·9% for >400 mm L _S fish. Most of the prey was represented by age 1 year fish, showing a unimodal body size distribution with a mode at 121–130 mm. Although cannibal body size was larger in deeper (>150 m) water, there was no difference in prey size by depth, suggesting impingement of the predators inhabiting deeper water into the shallow areas to cannibalize 1 year fish. The minimum ratio cannibal: prey size was 1·74. There was a positive but non-significant correlation between the contribution of cannibalism to a potential predator's (>300 mm) diet and an estimate of the previous year's recruitment. This was due to an extremely high contribution of cannibalism during 1992, when a distinctly larger size of predators seemed to bias the contribution. When the 1992 data were removed from the analysis, a significant correlation was obtained ( r ²=0·77, P <0·01), showing that Pollock cannibalism is rather density dependent. Based on the results, it is hypothesized that the'overflow' of 1 year fish from the shelf waters due to their high abundance and the weak stratification in the spring water column results in increased co-occurrence with adult fish and consequent cannibalism.     

Otolith-based analysis of survival and size‐selective mortality of stocked 0+ year pike related to time of stocking

The effect of time of stocking on the extent and source of mortality in 0+ year pike Esox lucius was investigated in a lake (20 ha) and a drainable pond (0·5 ha) using pike with alizarin marked otoliths. The results indicated that pike stocked late relative to the recruitment of native 0+ year pike fell victim to cannibalism from these larger individuals. This resulted in very low survival through the first growing season (<2%). Pike stocked early in the season exhibited significantly higher survival (>12%). Analyses of the size distribution of the alizarin marks from these fish revealed that the largest 0+ year pike exhibited by a factor of 3·3, higher survival than the average 0+ year pike in the lake. In order for large 0+ year pike to exhibit such high relative fitness a minimum of 69·7% of the original population must suffer size dependent mortality. In the pond the survival of the largest pike was by a factor of 4·2 higher than the average pike, and the corresponding size dependent mortality was 76·4%. The substantial size‐dependent mortality was most probably due to intra‐cohort cannibalism or habitat segregation between large and small 0+ year pike that exposes the small pike to predatory fishes in the open lake. Cannibalism exerts a major influence on the survival of 0+ year pike post‐stocking although the magnitude and origin differ in relation to stocking time.     

Reproductive biology, length-weight relationship and relative condition of pond raised Tilapia zilli (Gervais)

In 'runted' populations of Tilapia zilli positive correlations were found between maturation stages and the following: gonadosomatic index, gonad weight, fish weight and fish length. The minimum size at maturity was 9·0 cm in males and 11·0 cm in females. The mean fecundity in the 'stunted' females was 2359 eggs and it increased with length ( L ) weight (HO and depth ( D ) of the fish. There was, however, no correlation between fecundity and egg size. The results indicated that growth in this 'stunted' T. zilli population was not isometric. The relative condition factor ( Kn ) which approached one indicates good condition.