Age and growth analysis of the mosshead sculpin Clinocottus globiceps Girard 1857 (Pisces: Cottidae) from Helby Island, British Columbia

The age and growth of the cottid fish Clinocottus globiceps Girard from tidepools at Helby Island, British Columbia, Canada were investigated with the aid of whole saccular otoliths (sagittae); ages were validated by marginal increment analysis. Four hundred and twenty five specimens were examined from 214 females and 211 males. Marginal increment analysis on specimens with one to three opaque zones suggested an annual ring deposition in sagittae during the late autumn and spring months.
The C. globiceps population was composed of individuals from less than 1 year to 5 years of age for fish measuring between 5–120 mm standard length. Growth was faster for younger than for older age groups. Lengths-at-age data were fitted to the Gompertz growth model, and estimates of the model parameters L₀, G and g were 26.7 mm 1.58 and 0.30 for pooled cohorts, respectively. The highest levels of growth occurred during late spring and early summer, when water temperatures were at maximum and food was most abundant. The lowest levels of growth occurred during the autumn and winter months.     

Somatic growth and otolith growth in juveniles of a small subtropical flatfish, the fringed flounder, Etropus crossotus

A growth experiment was conducted with juvenile fringed flounder (Etropus crossotus) from North Inlet (South Carolina, USA) to provide information on the growth of a small, shortlived flatfish with a subtropical and tropical distribution. The fringed flounder has a maximum life span of 1.5 y and its long spawning period from March through October complicates the determination of growth rates based on length frequency data. Otoliths of juveniles with a standard length (SL) 23.1-53.0 mm were marked with Alizarin complexone and the fish were held in the laboratory for 66 days at 14, 20, 24 and 29 degrees C while being fed ad libitum. The mean somatic growth increased with temperature from 0.1 mm SL day(-1) at 14 degrees C to 0.4 mm SL day(-1) at both 24 and 29 degrees C. The maximum observed somatic growth rate was 0.7 mm SL day(1) at 29 degrees C. The number of micro-increments formed in otoliths was not significantly different from the expected value, validating formation of one increment per day. The significant relationship between increment width and somatic growth rate can be used to estimate somatic growth rates of individual wild fish based on daily increment information in their otoliths.     

Morphological changes during metamorphosis in cod (Gadus morhua L.), with particular reference to the development of the stomach and pyloric caeca

Metamorphosis in cod, Gadus morhua L., was investigated with respect to morphological changes in the alimentary tract (mouth, stomach and pyloric caeca) and external characters (finfold and fin development). Morphometric measurements and histological investigations were made on both larvae and juveniles and all fish lengths are given as standard length. Median unpaired fins started to develop when the fish were 9–10 mm in length. The larval median finfold was resorbed when fish reached a size of 11–15 mm. The vertebrae were formed in fish of 11–20 mm. The supraterminal mouth, seen in larvae <12 mm, changed gradually to a sub-terminal position in juveniles larger than 65 mm. The development of the stomach and pyloric caeca started at 15 mm and the juvenile form was seen in fish of 40 mm. The ability to store and grind food particles in the stomach developed gradually as fish increased in size from 20 to 40 mm. Compared to many other teleost species, cod juveniles are relatively large when the stomach and pyloric caeca become fully developed. These findings may have important implications for both start-feeding of cod larvae and the weaning of juveniles on to artificial diets.     

Habitat, reproductive biology and size composition of Parequula melbournensis, a gerreid with a temperate distribution

Trawling was carried out over sandy substrates in the shallow (5–15m) and deeper (20–35m) waters of four regions along 250 km of the lower west coast of Australia, during seven consecutive seasons. This yielded 32 752 individuals of the gerreid Parequula melbournensis , which constituted c. 42% of the total number of fish. Densities of P. melbournensis were greatest in the most southern region, reaching a seasonal maximum of 835 fish ha⁻¹: at one site in that region. Since P. melbournensis is restricted largely to the southern coastline of Australia, it has a temperate rather than subtropical or tropical distribution and thus is not a typical gerreid. Furthermore, unlike most other gerreids, it does not spend part of its life cycle in either estuaries or nearshore marine waters. The maximum total length of P. melbournensis was 175 mm, with the length at maturity ( L ₅₀) being 115 mm in females and 121 mm in males. No clear monthly trends were exhibited by gonadosomatic indices, the prevalence of mature ovaries and the oocyte size-frequency distributions of female P. melbournensis , and no clear and consistent modes were observed in length-frequency data for this species. These strong indications that spawning occurs throughout the year were substantiated by the occurrence of post-ovulatory follicles in the ovaries of large fish in all months but August, and by the presence in that month of advanced yolk granule oocytes in some ovaries, which implies that spawning was imminent. The spawning of P. melbournensis throughout the year contrasts with the far more restricted spawning periods recorded for other teleosts in the same temperate Australian waters. In this respect, P. melbournensis exhibits the characteristics of the essentially tropical family to which it belongs. Annuli, which could be detected on the otoliths of c . 40% of fish, suggest that the majority of P. melbournensis Were <3 years old.     

Morphometric analysis of otoliths of juvenile crucifix sea catfish Sciades proops (Valenciennes, 1840)

The objective of this study was to analyze the morphometry of otoliths for Sciades proops juveniles by testing the hypothesis of equality in morphometric relationships for the right and left otoliths, which could then be interchangeably used to estimate fish size or weight. Samples were obtained monthly directly from anglers after each event that took place off the state of Sergipe from March/2014 to April/2015. Anglers used rod and reel during these events, with no restriction on hook size or line thickness. Each fish specimen sampled had their total weight (W, g) and total length (TL, cm) measured and their lapillus otoliths removed and stored separately. Each otolith had its length (OL), width (OWi), and thickness (OT) measured (all in mm) under a stereomicroscope. Otoliths were weighed using a precision scale (OW, g). A total of 883 specimens were sampled: TL = 12.0–60.5 cm and W = 9.8–1880 g. The weight‐length relationship for the juvenile fishes was W = 0.0052TL^3.086 and for their otoliths was OW = 0.0002OL^3.177. The weight‐length and length‐length relationships fitted for each otolith (right and left) were not statistically different and thus all relations were estimated for grouped otoliths. The length‐length relationships for the otoliths were: OWi = 0.947OL?0.205 and OT = O.484OL?0.698. The relationship estimated for juvenile fish and otolith weight was Wj = 1076.1OW?9.120. For juvenile fish total length and otolith length, width and thickness, the following relationships were estimated: TLj = 4.028OL?3.199, TLj = 4.208OWi?2.091, and TLj = 7.824OT + 3.659, respectively. Relationships between fish and otolith size, and between fish and otolith weight indicated a change in slope close to L_m50, which should be better explored when more adult specimens are available.     

Validation of daily otolith increments in larval and juvenile Chinese sucker, <Emphasis Type="Italic">Myxocyprinus asiaticus</Emphasis>

Otolith development was observed and the formation of daily growth increments in otoliths of Chinese sucker, Myxocyprinus asiaticus, was validated by monitoring known-age larvae and juveniles in the laboratory from 2003 to 2005. Otolith shape changed with larval and juvenile development, and there was an exponential relationship until a body length of 16 mm or so, and a linear relationship after a body length of 16 mm between otolith size and fish size. The first increment was identified in larvae 1 day after hatching. The regressed equations between daily age (D) and increment number in otoliths (N) were N = −0.64 + 0.96D in lapillus, and N = −0.31 + 0.98D in sagitta. The slopes were not significantly different than 1.0. This demonstrated that otolith increments in this species were formed daily and can be used for daily age determination.     

Validation of daily increment formation in otoliths of juvenile and adult European anchovy

The otoliths of juveniles and adults of European anchovy Engraulis encrasicolus held in aquaria were marked by immersion in oxytetracycline hydrochloride (OTC) at concentrations between 350 and 410 mg l⁻¹ for 12 h. Counts of microincrements between fluorescent bands validated the daily otolith increment formation. The otolith increments were easily readable at ×400 with average increment widths of c . 1·1 µm. Validation was successfully demonstrated in juveniles and adults maintained for short periods in the aquaria in the summer. For European anchovy captured as juvenile and reared to adults, however, increment formation appeared less than daily. The daily periodicity of the otoliths in juvenile European anchovy implies that counting of microincrements can be used to study their birth dates. The application of this technique to adults, however, may lead to the underestimation of actual age and further research needs to be done to clarify the reasons for the apparent loss of the daily rhythm over long periods.     

The biology of Boyer's sand smelt, Atherina boyeri Risso in the Bardawil Lagoon on the Mediterranean coast of Sinai

The present study describes some aspects of the life history of Boyer's sand smelt Atherina boyeri in the hypersaline Bardawil Lagoon on the Mediterranean coast of the Sinai peninsula, Egypt. Monthly samples were collected with a small-mesh experimental beach-seine during the years 1973–1974. Age determinations were based on otoliths readings and length frequency distributions which indicate that the Bardawil Lagoon population consists mostly of 0-age group. The largest recorded fish was 63 mm in standard length (S.L.). Length-weight relationship has been calculated as: W = 13.7 × 10⁻⁶× L ^2.93 where W = weight (g) and L =S.L. (mm). Atherina boyeri mature at the length of 34 mm. Spawning takes place from March to September. The average number of eggs in the ovary of a ripe female at the beginning of the spawning season was found to be 522. Females of all sizes were more numerous than males. In immature fish, less than 34 mm long, females constituted 53% of the population. In larger fish the number of females was higher; in fish over 34 mm long females constituted 64% and in fish over 51 mm—96%. Atherina boyeri in the Bardawil Lagoon feeds on both zoobenthos and zooplankton, mainly amphipods and copepods. Polychaetes, mysidaceans, insects and fish were also represented. Atherina boyeri is the host of endoparasitic Trematoda, Acanthocephala and Nematoda. The examined fish were found to have metacercaria in their mesenteries and liver.     

Assessment of errors associated with harbour seal (Phoca vitulina) faecal sampling

Six harbour seals, ages 4–8 years, were held as pairs in a 10 times 20 times 2 m tank filled with sea water, and on 60 occasions were fed a meal of a specific species of fish or cephalopod of known size. The tank was drained periodically, and harbour seal faeces were collected on a 0.5 mm sieve. Number and size of otoliths and beaks found in faeces were determined. Fifty-eight percent of 670 fish and 37% of 36 cephalopods fed to harbour seals were represented by their otoliths or beaks in faeces. Estimated number of prey consumed was determined from the greatest number of left or right otoliths or upper or lower beaks collected in faeces. Estimated length ofprey was determined from measurements of otoliths and beaks recovered in the tank and relationships of otolith and beak measurements to prey length. Estimated number of fish eaten was not significantly different among pairs of harbour seals, but was different among species of fishes. Only 24–35% of fish species with small otoliths were represented in faeces, whereas more robust otoliths from other species were less apt to be completely dissolved. Estimated length of fishes was significantly less than lengths of fishes fed to harbour seals in 39 (76.5%) of 51 trials. Cephalopod beaks were not affected by passage through the harbour seal digestive tract. Amount of otolith dissolution was not related to species of fish; estimated fish length was underestimated by an average 27.5%. Although some (7.4%) of the otoliths were collected within 100 h after the fish were ingested, more than 90% were recovered within 24 h after the fish was eaten. Correction factors were developed which will allow researchers to estimate more reliably number and size of fish and cephalopod prey eaten by harbour seals.     

Historical changes in juvenile southern bluefin tuna Thunnus maccoyii growth rates based on otolith measurements

Suspected historic changes in juvenile southern bluefin tuna Thunnus maccoyii growth rates were investigated using otolith increment width data. Four hundred and ninety otoliths were selected from fish estimated to be between 1 and 41 years-old. The distance between the first five annuli were measured on the otoliths, giving estimates of otolith growth for age classes 1+ to 4+ years for fish spawned from the early 1960s to mid 1990s. The data showed that growth rates of juveniles (age 1+ and 2+ years) started to increase at around 1979–1980, and that growth continued to increase throughout the 1980s and early 1990s. Lee's phenomenon was not observed in the data. Correlation tests did not reveal clear relationships between annual otolith growth and regional environmental variables such as sea surface temperature or Southern Oscillation Index. The increase in otolith growth, however, was consistent with juvenile growth estimates obtained from other sources, and correlated with large-scale trends in population size and environmental conditions.     

Age and growth of Lutjanus kasmira (Forskål) in Hawaiian waters

The growth of Hawaiian taape, Lutjanus kasmira , was studied by examining otoliths and by analysing length-frequency distribution. Annual hyaline and opaque markings were visible in whole mounts of sagittae, which were verified by enumeration of daily increments with a scanning electron microscope (SEM) and through marginal increment analysis. The von Bertalanffy growth curve was fitted to the data, resulting in: where t. l . is total length (cm) and t is age (years). SEM observations revealed that the slowgrowth hyaline zones were composed of daily increments too small (0.4–0.8 μm) to be resolved optically. Thus, age estimates derived by numerically integrating otolith growth rate data obtained with a light microscope showed a negative bias, resulting in overestimation of growth rates. Parameter estimates obtained from three different types of length-frequency analysis were also unstable. This was due, at least in part, to differences in the size composition of fish sampled with different fishing gears and from different depths.
The growth rate registered in Hawaii falls within the reported growth coefficients of lutjanids, whereas it is one of the highest in the Pacific and clearly higher than a deep-water lutjanid species growth in Hawaii. Probably, this high growth rate may have been enhanced by the relative lack of competitors in the depauperate Hawaiian marine fish community.     

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.     

Validation of daily increment formation in otoliths for three Diplodus species in the Mediterranean sea

The efficacy of two fluorochromes, chlorhydrate of tetracycline (CHTC) and alizarin complexone (ALC), to induce a label on the otoliths of juvenile sparid fishes by immersion techniques was tested in different experimental conditions. CHTC did not mark otoliths in natural sea water and was toxic in divalent cation-free sea water. Immersing fish in a 50-mg 1⁻¹ ALC natural seawater solution for 24 h induced a well-defined mark on the otoliths and had no effect on survival. A daily periodicity of increment formation on otoliths was observed in captivity for Diplodus vulgaris and D. puntazzo , and was conserved in natural environment for D. sargus . The frequency of increment deposition did not vary with the age of juvenile fishes. Thus, otolith microstructure analysis will be a reliable method to give age estimates in these three sparid species during their juvenile life.     

The potential for intracohort cannibalism in age-0 walleye pollock,Theragra chalcogramma,as determined under laboratory conditions

Synopsis In laboratory experiments, we tested the capability of larger age-0 walleye pollock to consume smaller members of their cohort. In separate aquaria, 81 pairs of juveniles covering a wide range of size differences (total lengths differing by 12 to 61 mm) were held and monitored over a 4 day period. Complete consumption, in which a smaller fish was swallowed whole by a larger fish, occurred 11% of the time. In 36% of the pairs, attacks by the larger fish resulted in mortality of the smaller fish. The mouth width:body depth ratio between the larger and smaller fish of a pair differed significantly depending on whether the smaller fish survived, was killed but not consumed, or was ingested whole by the larger fish. Cannibalistic individuals could consume fish close to the maximum size physically possible under gape limitation; at this size the length of the cannibal was approximately 1.7 times the length of the prey. Length-frequency distributions of age-0 pollock in field concentrations suggested that, at least in some geographical areas, potential cannibals and prey commonly co-occur. Unsuccessful predatory attacks by larger individuals may have additional detrimental effects on smaller pollock in natural populations.     

Food of the emperor penguin Aptenodytes forsteri on the Antarctic fast ice edge in late winter and early spring

Summary The food of emperor penguins Aptenodytes forsteri at the edge of the sea ice off the Vestfold Hills was studied by faecal analysis. Fish, crustacean, cephalopod and gastropod remains were found in 151 droppings collected between August and October 1984. The main fish identified from otoliths was Pleurogramma antarcticum with an average standard length of 129.5 mm. Amphipods increased in frequency from August to October with gammarids predominating.     

Influence of different rations and water temperatures on the growth rates of shortfinned eels and longfinned eels

Juvenile (12–152 g) shortfinned eels Anguilla australis and longfinned eels A. dieffenbachia caught in New Zealand streams were fed squid mantle Nototodarus spp. 4 days per week in laboratory experiments. A linear multiple regression equation showed the amount of food eaten (0–2·7% w day⁻¹) explained 77·7% of the variation in specific growth rates (–0·60 to +1·07% w day⁻¹) among individual eels, while previous growth rates, water temperature (10·0–20·6°C), and eel weight (12–152 g) explained a further 5·6, 1·4 and 0·8%, respectively. Growth in length ranged from –0·3 to +0·9 mm day⁻¹. Eels which were starved and then given high rations grew substantially faster than expected. Once growth rates were adjusted for differences in ration and other factors, there were no significant differences in growth rates between species or individual fish. Growth of shortfinned eels fed maximum rations of commercial eel food depended on fish size and water temperatures and ceased below 9·0°C. Growth rates in the wild were substantially less than the maximum possible, after seasonal changes in water temperatures were taken into account, indicating that food supplies and not low water temperatures were controlling growth rates in the wild.     

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.     

Growth in the crayfish Austropotamobius pallipes (Crustacea: Astacidae)

SUMMARY. The growth of Austropotamobius pallipes was studied in the River Ouse during 1976–78. Growth of mature crayfish (>2.5 cm carapace length) was followed by determining the relationship between the growth increment at moult and premoult carapace length, together with the frequency of moulting of different categories of crayfish. These data are supplemented by the recapture of marked individuals and the measurement of crayfish held in corves in the river. Growth was limited to the period May–October when water temperatures exceeded 10°C. Growth rates of male and female crayfish are similar until maturity is reached, thereafter males moult twice per year and the majority of females moult once. No crayfish in excess of 3.7 cm carapace length has been observed to moult more than once per year. Growth of juveniles (<2.5 cm carapace length) was estimated from size frequency distributions constructed from regularly taken samples. Growth rates of juveniles showed great variation both between and within year classes. In the hot dry summer of 1976, juveniles exhibited faster growth rates (instantaneous growth rates (G) for 0+ and 1 + crayfish were 0.029 and 0.013 mg mg⁻¹ day⁻¹. respectively) than in other years. Laboratory experiments on the effect of temperature on the growth rate of 0 + crayfish were undertaken; for crayfish at 15°C. G = 0.0138 (0–53 days) and at 10°C, G = 0.0003 (0–90 days). Crayfish held at 10°C failed to undergo a single successful moult. At 20°C crayfish exhibited exponential growth over the first 40 days, with G = 0.0189. declining thereafter to G = 0.012 (40–90 days).     

The ontogeny of schooling behaviour in the striped jack

The ontogeny of schooling behaviour was investigated in laboratory-reared striped jack Pseudocaranx dentex larvae and juveniles. Mean separation angle between nearest individuals averaged 78 and 82° in 10- and 12-mm fish, respectively, and decreased to 57° in 16-mm fish. In addition, interindividual distance decreased from three times body length in 12-mm fish to twice the body length in 16-mm individuals; this value continued to decrease gradually to 1·3 at 19 mm to 0·79 at 30 mm. Mutual attraction due to visual recognition was observed in 12-mm fish and increased with total length. The optokinetic response ( R_o , the ability of a fish to keep station with moving patterns) first appeared in 4–6-mm larvae. In spite of the traditional emphasis of the importance of R_o in schooling behaviour, the onset of R_o was insufficient to result in school formation. The emergence of mutual attraction seems essential for the ontogeny of schooling.     

Growth and development of a bimodal length-frequency distribution during smoking in a wild population of white-spotted charr in northern Japan

Smolt age and size, and individual growth during smoking were examined in a wild population of white-spotted charr, Salvelinus leucomaenis , in a small stream in northern Japan. Smolt size (110–210 mm F.L.) differed neither between sexes nor among age cohorts of 2–7 years. Back-calculation of riverine growth of smolts using otoliths showed a gradually increasing discrepancy in fork lengths of these age cohorts in both males and females, the faster-growing individuals smolting at an earlier age. A mark—recapture study on individually-identified fish revealed that the initial (spring-summer) length-frequency distribution of parr was unimodal, but became slightly skewed to the larger side in autumn, resulting in a bimodal distribution being evident by the following spring, with the upper modal group primarily composed of smolts. However, closer examination revealed that both male and female potential (subsequent) smolts were larger than the potential parr in the previous spring, the minimum lengths of the former being around 90–100 mm f.l. Specific growth rates of the potential smolts remained relatively high after summer through to the following spring, whereas those of the potential parr decreased after summer, despite having been similar between the two groups during the previous spring and summer. These observations revealed that the developmental triggering of smelting possibly occurs in or following the summer season.