Effects of river flow on larval growth and survival of Japanese seaperch Lateolabrax japonicus (Pisces) in the Chikugo River estuary, upper Ariake Bay

The abundance and growth history of larval and juvenile Japanese seaperch Lateolabrax japonicus were investigated in the Chikugo River estuary, upper Ariake Bay, from 1990 to 2000. Growth during the larval period (up to 15 mm standard length, L _S, the size at recruitment into the estuary) was backcalculated using sagittal otolith microstructures by the biological intercept method. Growth rates in length declined at body sizes >14 mm L _S. High freshwater discharge through the Chikugo River was associated with high temperatures of the upper Ariake Bay where the larvae spend their planktonic life. Mean larval stage duration (days) from hatch to 15 mm ( D ₁₅) varied between 48·8 and 76·2 days and was inversely correlated with the estimated mean temperature history [mean daily temperature (° C) experienced by the larvae during the period from hatch to 15 mm, T ₁₅]. Mean abundance (number m⁻²) of larvae and juveniles was highest in years when T ₁₅, D ₁₅ and freshwater discharge were at intermediate levels. Although the abundance was not correlated with either of these variables, an exponential relationship between abundance and D ₁₅ was found when data collected during the highest river discharge years (1990, 1991 and 1998) were excluded. The increase in freshwater discharge through the Chikugo River probably had the potential to enhance or diminish Japanese seaperch recruitment in two ways: 1) it could increase recruitment probability by increasing temperature and larval growth and 2) high river flow also had the potential to decrease the probability of immigration into the river by increasing larval seaward dispersion, predation due to decreased turbidity and starvation due to decreased zooplankton prey abundance in the estuary.     

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.     

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.     

Fluctuating asymmetry in the otoliths of larval Atlantic menhaden Brevoortia tyrannus (Latrobe) – a condition indicator?

Fluctuating asymmetry (FA) was described for otolith length, width and area for two groups of larval and juvenile Atlantic menhaden Brevoortia tyrannus. The larvae and juveniles (age range: 20–120 days; standard length, L _S, range: 14–35 mm) were separated into the two distinct groups a priori on the basis of their growth indices estimated from residuals of a L _S-at-age model; slow growers had residuals <8% of the average size at age and fast growers had residuals >8%. Some indication supporting the fluctuating asymmetry methodology was found when unsigned normalized FA2 index was used for otolith area. That conclusion was not, however, supported by the other method used in this work, i.e. between-group ANCOVA analysis of individual unsigned and not normalized FA1 indices plotted against trait size. These inconsistent results are most probably a consequence of error introduced during FA index normalization (accounting for trait size effect on absolute FA). Although it is concluded here that FA analysis of sagittal otoliths was not effective in describing differences in the natural variability of growth and condition of larval Atlantic menhaden, the possible species- and otolith type-related differences should be considered in the future research on FA.     

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.     

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.     

Comparison of growth rate and formation of otolith increments in age-0 red snapper

For wild red snapper Lutjanus campechanus , mean otolith increment deposition rate after marking with oxytetracycline dihydrate (OTC) was daily (0.97 increments day⁻¹) when growth rates were fast (0.63 mm fork length, L _F day⁻¹), but were not daily (0.82 increments day⁻¹) when somatic growth was slow (0.2 mm L _F day⁻¹). For reared larvae ( n =8), increment deposition rates were daily (0.99–1.03 increments day⁻¹), and growth rates ranged from 0.6 to 0.9 mm L _F day⁻¹. Growth rate affected increment deposition rate as a threshold function, i.e. when growth rate was <0.3 mm L _F day⁻¹, deposition was less than daily, but above this level increment deposition did not exceed a daily rate. As growth rates increased increment widths increased. Examination of a sub-sample ( n =8) of the otoliths from the slowest growing wild fish by scanning electron microscopy did not increase increment counts. Because L. campechanus are late spring-early summer spawners, young fish can expect maximum growth due to warm summer temperatures. Thus, daily ageing methods should be well suited to this species.     

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.     

Gape morphology of cod Gadus morhua L., haddock Melanogrammus aeglefinus (L.) and whiting Merlangius merlangus (L.) through metamorphosis from larvae to juveniles in the western Irish Sea

Variations in standard length ( L _S), gape size ( S _G) and jaw length ( L _J) were studied in larval and juvenile gadoids (cod Gadus morhua , haddock Melanogrammus aeglefinus and whiting Merlangius merlangus ) from 4 to 70 mm. The increase in S _G and L _J was not linear with respect to L _S. The relationship was best described by segmented regression lines in all three species, with an inflection point at c . 10·5 mm. The S _G and L _J increased more rapidly in relation to larval L _S for individuals smaller than this inflection point size. The rates of increase slowed significantly post-inflection, an effect more noticeable in S _G data compared to L _J data. In each case, the inflection point fell in the intermediate period of development between the larval and juvenile stages, which could be considered as metamorphosis. Published equations that have been used to predict S _G from L _J lead to the overestimation of gape. New relationships are presented, which may be used to predict S _G from measurements of either L _S or upper jaw length in cod, haddock and whiting.     

Early development and growth of the laboratory reared north-east Atlantic mackerel Scomber scombrus L.

The early development, growth and morphological changes of mackerel Scomber scombrus were investigated at different incubation temperatures (8, 10, 13, 15 and 18° C). Details on the early life history are illustrated with special reference to morphological transformations. Culture techniques to rear larval mackerel stages are described using laboratory cultured foods. Artificially fertilized eggs were hatched after 80·6 h at 18·4° C and 256·8 h at 8·7° C. The standard length ( L _S) of the individuals at first feeding was 4·71 ± 0·18 mm. Four mortality critical periods and cannibalistic behaviour were identified. A maximum average larval size of 37·5 ± 4·41 mm L _S was attained 30 days post-hatch (dph) at 18·4° C. Development and growth were affected significantly by temperature during both endogenous and exogenous feeding periods. Larvae grew more rapidly at high, than at low temperatures. Daily specific growth rate (in mass) ranged from 2·4% at 10·6° C to 16·9% at 18·4° C. Likewise, average growth rate (in length) ranged from 0·05 mm day⁻¹ at 8·4° C to 0·37 mm day⁻¹ at 18·4° C. The allometric relationship of L _S, with several body measurements was not affected by temperature. Comparison with larvae collected in the Bay of Biscay did not show any significant difference in the dry mass and L _S relationship; conversely, the growth rate in length differed significantly between both laboratory and field conditions. The trends observed in the laboratory are described in relation to some aspects of the year-class strength regulation.     

Consumption and gut evacuation rate of laboratory‐reared spotted seatrout (Sciaenidae) larvae and juveniles

The temperature and mass dependence of maximum consumption rate was measured for larval and early juvenile spotted seatrout Cynoscion nebulosus . Maximum consumption ( C _MAX) estimates were obtained from feeding and gut evacuation experiments on larvae (3·8–19 mm standard length, L _S) at three temperatures (24, 28 and 32° C), and maximum consumption experiments on juveniles at three temperatures (20, 26 and 32° C). Feeding levels were determined for larvae fed live prey ( Brachionus plicatilis and Artemia salina ) ad libitum . The midgut and total evacuation times were estimated for fish feeding continuously and discontinuously using alternate meals of tagged and untagged live prey. Temperature and fish size had significant effects on gut evacuation and consumption. The gut evacuation time increased with increasing fish size, and decreased with increasing temperatures. Mass‐specific midgut contents increased for small larvae <0·156 mg dry mass ( M _D)( c . 4 mm L _S), and decreased for larger larvae and juveniles. Maximum consumption was modelled by fitting a polynomial function to a reduced dataset of individuals feeding at high levels. The C _MAX model predicted an initial increase in specific feeding rate from 70 to 155% M _D day⁻¹ for small larvae, before declining for larger larvae and juveniles.     

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.     

Nutritional condition and vertical distribution of Baltic cod larvae

Newly hatched Baltic cod Gadus morhua larvae are typically found at depths >60 m. This is a region of low light and prey availability, hence generating the hypothesis that larvae have to migrate from hatching depth to the surface layer to avoid starvation and improve their nutritional condition. To test this hypothesis, Baltic cod larvae were sampled during the spawning seasons of 1994 and 1995 with depth-resolving multiple opening/closing nets. Each larva was aged by otolith readings and its RNA/DNA ratio was determined as a measure of nutritional condition. The RNA/DNA ratios of these larvae aged 2-25 days (median 10 days) ranged from 0.4 to 6.2, corresponding to levels exhibited by starving and fast-growing larvae in laboratory calibration studies (starvation, protein growth rate, G_pi= -12.2% day⁻¹; fastgrowing larvae, G_pi=14.1%day⁻¹) respectively. Seventy per cent of the field caught larvae had RNA/DNA ratios between the mean values found for starving and fed laboratory larvae. Only larvae aged 8-11 days had higher mean RNA/DNA ratios above 45 m than below ( t -test, P<0.05). However, the instantaneous protein growth rates were significantly higher for all larval age groups in the surface layers ( t -test, P<0.05). Starving larvae were found in all depths sampled (10-85 m), whereas growing larvae (positive G_pi) were restricted to samples taken shallower than 45 m. These superior growth rates above 45 m corroborate the hypothesis and imply that migration to the shallow water layers is a prerequisite for good nutritional condition, growth and survival of Baltic cod larvae. The frequent occurrence of cod larvae older than 8 days in the deep water in poor condition suggests that a proportion of the larvae will die from Starvation in the deep layers of the Baltic Sea.     

Ontogenetic development of electric-organ discharges in a mormyrid fish, the bulldog Marcusenius macrolepidotus (South African form)

The emergence and development of the electric-organ discharge (EOD) in larvae and juvenile bulldog Marcusenius macrolepidotus was investigated. Larvae hatched 4–5 days after spawning, and the first EODs were recorded on days 9 and 10 at a standard length ( L _S) of c. 6·5 mm. The larval EOD waveform was virtually monopolar, with a strong head-positive phase followed by a weak head-negative phase of long duration. A small separate potential preceded the EOD by c. 1·6 ms (believed to represent postsynaptic potential from electrocyte stalks). In contrast to previous reports on Pollimyrus adspersus with its distinct larval and adult EODs, in M. macrolepidotus there was a gradual transformation of the larval into the adult EOD waveform. The transformation started at an L _S of c. 17 mm (at an age of c. 40 days), first indications being a decrease in duration of the head-negative phase, and an increase of its peak amplitude relative to that of the head-positive phase. Still later, the weak postpotential of the adult EOD emerged on the rising edge of the head-negative phase. The transformation was nearly completed at an L _S of c. 30 mm (at an age of c. 60 days). Evolutionary and behavioural consequences of this alternative path of EOD ontogeny are discussed.     

Otolith microstructure during the pelagic, settlement and benthic phases in burbot

During the pelagic larval phase of burbot Lota lota L., the pattern of otolith increments changes, showing three, clearly distinguishable growth sectors: a first sector with faint increments, difficult to enumerate, comprising an average (±S.D.) of 17˙5±6˙7 increments, a second sector with distinct increments comprising an average of 33˙1±7˙6 increments and a third sector where increments again become faint and difficult to enumerate. Laboratory experiments conducted in parallel to the field investigation showed that settlement occurs after the formation of this third, faint sector and is marked by the formation of numerous accessory growth centres within the range of three to five daily increments. There was a strong linear relationship between sagittal width and total length of the burbot (r²=0˙928) over the range examined. Significantly different growth rates were calculated for the three otolith sectors (faint, distinct, faint) in burbot larvae, indicating large environmental changes during their pelagic larval phase in Lake Constance. These results suggest that inshore migration of burbot larvae does not take place in the warm epilimnetic surface waters but via an alternative pathway, the cold hypolimnion or profundal zone.     

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 the clupeid fishes, Stolothrissa tanganicae and Limnothrissa miodon, in the Zambian waters of Lake Tanganyika

The age and growth of two endemic Lake Tanganyikan clupeid fishes, Stolothrissa tanganicae and Limnothrissa miodon , were estimated from analysis of otolith microstructure in specimens collected in Zambian waters from October to December 1990. Both species had relatively clear, concentric otolith increments which were believed to represent daily increments based on their similarity to daily increments found in some marine clupeid species. The growth rates estimated from length-at-age data were: for S. tanganicae, L_t = 104·0 (1 – exp (– 0.00512 ( t – 5·8))); for L. miodon, L_t = 155.4 (1 – exp (– 0.00236 ( t +8.1))). In most cases, the growth parameters obtained from otolith analyses generally agreed with those previously estimated from analyses of length-frequency distributions.     

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.     

The feeding ecology of Morone americana larvae in the Chesapeake Bay estuarine turbidity maximum: the influence of physical conditions and prey concentrations

Feeding ecology of white perch Morone americana larvae, a major component of the ichthyoplankton community in the estuarine turbidity maximum (ETM) region of upper Chesapeake Bay, was evaluated in years of contrasting physical conditions. In 1998, high river flow led to an ETM with high turbidity and pronounced salinity stratification. In 1999, under low river flow conditions, turbidities in the ETM region were lower and the salt front was located 15 km up‐stream of its location in 1998. Copepodites and adults of Eurytemora affinis were the predominant prey in guts of all length classes of larvae (3·2–9·8 mm standard length, L _S) that were examined. Repeated‐measures, multiple regression analyses were conducted to evaluate the influence of several factors on feeding success by determining if physical conditions (temperature, current velocity, salinity, turbidity and light) and prey concentrations explained variability in mean gut fullness (gut contents mass per body mass) of small (<5 mm L _S) and large (>5 mm L _S) white perch larvae. Eurytemora affinis concentrations were significant in the statistical models for both small and large larvae. High concentrations of E. affinis , which enhanced encounter rates of white perch larvae with prey, may have been the most important factor determining feeding success in the ETM region. Larval feeding incidence (percentage of guts with food) was higher in 1998, suggesting that annual variability in river flow influenced larval feeding success by controlling physical and biological conditions in the ETM region.     

Does water calcium content influence the distinctness of daily growth increments in the otoliths of larval whitefish (Coregonus lavaretus L.)?

In larval and juvenile whitefish ( Coregonus lavaretus L.) from Lake Constance, Germany, the otolith increments are deposited daily, whereas daily deposition could not be confirmed in larval whitefish from Lake Pyhäselkä, Finland. The calcium concentration in Lake Constance is high (around 1.3 m m ), while calcium deficiency is typical for Finnish lakes (around 0.15 m m ). Therefore, the hypothesis that the distinctness of daily otolith increments in whitefish is related to water calcium content was tested by rearing three groups of Lake Constance whitefish in water of 0.2, 1.3 and 4.7 m m Ca. The eggs were incubated in lake water (1.3 m m Ca), and the larvae were acclimated to the experimental calcium concentrations on the day of hatching. After 39 days of ad libitum- feeding with Artemia nauplii, the three groups did not differ significantly in total length, wet and dry weight, and otolith length and width. The daily increments were easily recognizable, and contrast between dark (D)- and light (L)-zones was the same in the fish of all test groups. For the experimental set-up of this study, and particularly the range of calcium concentrations tested, the hypothesis that water calcium content influences the distinctness of daily otolith increments was rejected.