Effects of water depth and hydrodynamics on the growth and distribution of juvenile cyprinids in the littoral zone of a large pre-alpine lake

In enclosure experiments in the littoral zone of Lake Constance, Germany, juvenile cyprinids showed significantly reduced somatic growth in the shallow eulittoral zone (0·5 m depth) compared to the sublittoral zone (1·6 m depth). Growth was especially reduced in larger and more deep-bodied fish groups, providing evidence that this is due to increased hydrodynamic stress, induced by ship and wind waves, in the shallow habitats compared to the deep habitat. Other factors such as water temperature and food availability seemed to be of minor importance for the observed growth differences. Gillnet catches at the experimental site and an adjacent site showed that most juvenile cyprinids, including the species from the enclosure study, bream Abramis brama and dace Leuciscus leuciscus , nonetheless prefer shallow habitats compared to deeper sublittoral habitats. Juvenile cyprinids in Lake Constance may prefer these shallow habitats as refuges against larger piscivorous predators, mainly perch Perca fluviatilis , despite the cost in terms of reduced somatic growth indicating that juvenile cyprinids first of all optimize survival rate instead of somatic growth rate.     

Energetic consequences of an inducible morphological defence in crucian carp

Crucian carp (Carassius carassius) increases in body depth in response to chemical cues from piscivores and the deeper body constitutes a morphological defence against gape-limited piscivores. In the field, deep-bodied individuals suffer a density-dependent cost when competing with shallow-bodied conspecifics. Here, we use hydrodynamic theory and swimming respirometry to investigate the proposed mechanism underlying this effect, high drag caused by the deep-bodied morphology. Our study confirms that drag is higher for deep-bodied crucian carp, both in terms of estimated theoretical drag and power curve steepness. However, deep-bodied fish swimming at the velocity associated with minimum cost of transport, U _mc, did not experience higher costs of transport than shallow-bodied fish. Deep-bodied crucian carp had significantly lower standard metabolic rates, i.e. metabolic rates at rest, and also lower U _mc, and the resulting costs of transport were similar for the two morphs. Nevertheless, when deep-bodied individuals deviate from U _mc, e.g. when increasing foraging effort under competition, their steeper power curves will cause substantial energy costs relative to shallow-bodied conspecifics. Furthermore, there is evidence that reductions in standard metabolic rate incur costs in terms of lower stress tolerance, reduced growth rate, and life history changes. Thus, this work provides links between hydrodynamics, a cost-reducing mechanism, and a density-dependent fitness cost associated with an inducible defence. Received: 22 March 1999 / Accepted: 14 June 1999     

Growth estimates from otolith increment widths of juvenile chinook salmon (Oncorhynchus tshawytscha) reared in changing environments

For otolith increments to provide useful estimates of fish growth, otolith growth must covary closely with somatic growth. We reared groups of juvenile chinook salmon ( Oncorhynchus tshawytscha Walbaum) for 70 days, changing ration or temperature during a 20-day treatment period. Restricted rations halted somatic growth, however increment widths decreased gradually; somatic growth was overestimated from increment width. Otolith growth followed changes in water temperature more closely than changes in ration, supporting a hypothesized effect of metabolic rate on otolith growth. Increment growth was only loosely coupled to fish growth rate, and may also be affected by past growth histories. For juvenile fish, increment widths may not be sensitive indicators of short-term changes in growing conditions.     

Ontogenetic and environmental effects on otolith shape variability in three Mediterranean European eel (Anguilla anguilla, L.) local stocks

Otolith morphology is an efficient tool for the discrimination of fish stocks, populations and species when comparative genetic data are not available. Currently, the relationship between environmental factors and otolith shape is poorly characterized for the European eel (Anguilla anguilla), a highly migratory catadromous species constituting a single, randomly mating stock. The present study analyses the differences in otolith morphology between three Mediterranean eel local stocks from different environmental contexts (i.e. two brackish lagoons and one river). The relationship between otolith shape and otolith size was studied by means of Elliptic Fourier analysis and multivariate statistics. Otolith profile was digitally acquired and Cartesian coordinates were extracted. Partial Least Square (PLS) analysis pointed to continuous allometric growth in size and shape in otoliths from all three sites. In the three environments, shape variations occurred during growth as indicated by the presence of a significant and positive relationship between otolith size and the first PLS latent vector (i.e. which bears most of the information regarding otolith outline). Differences between smaller and larger sized otoliths were investigated using PLS Discriminant Analysis (PLSDA) and cluster analysis. Results indicate that otolith shape is highly uniform at smaller than at larger sizes. These shape differences apparently overlap the initial differentiation of the small otolith outlines acquired by eels during the growing phase as elvers in the marine environment. Data were discussed considering that the physical and chemical habitat variability in brackish lagoons and river could underlie a marked change in otolith shape during the animals' growth.     

Effects of variable ration levels on direct and indirect measures of growth in juvenile red drum (Sciaenops ocellatus)

Relationships between somatic growth (length and weight) and two indirect measures of growth (otolith growth, RNA/DNA ratio) were assessed for red drum (Sciaenops ocellatus) under different feeding rations [0%, 2.5%, 5%, 10%, 15%, and 20% body weight (BW)/day] for 30 days. Representative samples from each ration level were taken in 10-day intervals between Day 0 and Day 30 for evaluation of direct and indirect growth measures. Positive correlations were observed between ration levels, somatic growth, and otolith growth. Statistical differences in weight and length of red drum were observed among ration levels by Days 10 and 20, respectively. Statistical differences for measures of otolith growth among ration levels were evident by Days 20 and 30. In addition, RNA/DNA ratios showed clear separation between fish that were starved and fish that were fed but demonstrated minimal separation among ration levels. Overall, the combination of a measure of somatic growth (weight) and a measure of otolith growth (otolith weight) resulted in the most statistical separation among ration levels. Findings from this study suggest that somatic growth, otolith growth and RNA/DNA ratios are suitable measures of relative growth of red drum; however, due to differences in sensitivity, caution must be exercised when using indirect growth (otolith growth, RNA/DNA ratios) measures to estimate recent growth.     

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.     

Restricted fish feeding reduces cod otolith opacity

The purpose of this work was to examine the effect of reduced feeding and constant temperature on cod otolith opacity. Three groups of juvenile cod were given restricted food rations at different times for 4 months, resulting in depressed somatic growth. Otolith opacity was measured on pictures of the otolith sections. The otolith carbonate deposited during the experimental period was generally opaque compared to the more translucent otolith material deposited prior to and after the experimental period, when the fish were kept in a pond and in sea‐cages at higher temperatures. Large variations in otolith opacity were found between individual fish both within groups and between groups. In two of the three groups significantly more translucent otolith material was deposited in response to reduced feeding. Our results show that variations in feeding and hence fish growth resulted in variation in otolith opacity, but the effect was minor compared to that of variations in ambient temperature. The combined influence of these effects, which both act on fish metabolism, are most likely controlling the seasonal opacity changes observed in wild fish. Our results help explain the variations seen in fish at constant temperatures.     

Variations in otolith patterns, sizes and body morphometrics of jack mackerel Trachurus japonicus juveniles

Variations in otolith patterns, sizes and body morphometrics of jack mackerel Trachurus japonicus juveniles were investigated. Under transmitted light, translucent (W(t)) and opaque otoliths (W(o)) were detected in juveniles collected from Wakasa Bay between July 2005 and April 2006, whereas only opaque otoliths (G(o)) were detected in Goto-nada Sea individuals between May and June 2006. Three groups of juveniles were distinguished based on differences in hatch season, otolith size and growth history, and body morphometrics. As T. japonicus has different spawning seasons according to spawning grounds, each group was estimated to hatch in different waters. Juveniles with W(t) otoliths were considered to have stayed in coastal habitat longer, as the hatch area was estimated to be near Wakasa Bay. Juveniles with W(o) and G(o) otoliths appear to recruit to coastal waters at larger size, since their hatch areas were estimated to be far from each collection area. Larger otoliths of W(t) were attributed to otolith accretion after the second growth flexion, which was observed only for W(t) . Standard length of W(t) fish at the second otolith growth flexion was estimated to correspond to recruitment size to coastal rocky reefs in Wakasa Bay. Body morphometrics were correlated with otolith size after removing body size effect, suggesting that morphological variations of T. japonicus juveniles were also associated with the timing of recruitment to coastal habitat.     

Mn<Superscript>2+</Superscript> concentrations in coastal fish otoliths: understanding environmental and biological influences from EPR

The Mn²⁺ concentrations in the sagittae otoliths of 12 fish families (and 19 species) that co-occur in a coastal area of southeastern Brazil (~21°S) were quantified using electron paramagnetic resonance (EPR). Inferences were made about the relationship between fish habitat and trace element incorporation. Inferences were made on the relationship between trace element concentration and otolith shape. The differences in Mn²⁺ concentrations among the species suggest that habitat (and feeding habits) might drive the incorporation of this trace element into fish otoliths, with higher values in bottom-associated fish species than in surface-associated species. In surface-associated fish species, the correlation between trace element concentrations and otolith shape was stronger than in bottom-associated species. Thus, while the Mn bioavailability in a fish’s habitat, especially from feeding resources, is a local driving influence of trace element incorporation in sagittae otoliths, species-specific requirements also have an influence. Quantitative EPR is a non-destructive technique that is very useful when the available samples cannot be damaged, like with otolith collections.     

Temperature effects on otolith pattern formation in Atlantic cod Gadus morhua

The effect of food intake and temperature on otolith macrostructure and microstructure was examined experimentally in Atlantic cod Gadus morhua. Daily increment formation was validated and otolith accretion rate and optical density quantified using image analysis. Two‐week periods of starvation had no discernable effect on otolith increment width or optical density, despite having negative effects on somatic growth. In contrast, temperature had a strong positive effect on otolith accretion rate and clear effects on optical density with the otolith becoming more translucent at higher temperatures. Somatic growth, otolith accretion and otolith optical density each had a significantly different response curve to temperature. No relationship was detected between individual somatic growth rates and the accretion rate or optical properties of the otolith. The experimental manipulation of temperature‐induced otolith patterns similar to the ‘false ring’ secondary structures sometimes observed in the otoliths of wild fish. The results suggest that otolith pattern arises from a combination of temperature and seasonal effects, but not directly from individual variation in somatic growth.     

Physiological variation in the dog-whelk Nucella lapillus, L. either side of a cline in allozyme and karyotype frequencies

Genetic constitution in the intertidal gastropod Nucella lapillus influences variation in shell shape and growth rate which in turn are correlated with such habitat variables as wave action and temperature. We have investigated the response to hyperosmotic stress of samples from a cline in karyotype and allozyme frequencies and shell shape. Animals with a shell shape associated with environments where temperature and desiccation stress are important respond less to hyperosmotic stress than animals living in a high wave energy environment. With regard to the interaction between shell shape, physiology and habitat, animals with elongate shells associated with protected shores are shown to exhibit a reduced response to hyperosmotic stress compared to animals with a more spherical shell shape; this is discussed in relation to the production of an adaptive phenotype.     

Otolith size changes related with body growth,habitat depth and temperature

Synopsis Size variation in the sagittal otoliths of six species of the genus Merluccius, and five species of the genus Coelorhynchus was compared, using a digital image processing system and multivariate analysis. It is proposed that otolith growth occurs under dual regulation, overall shape is regulated genetically, and otolith size is influenced by environmental conditions. The decline of temperature with increasing habitat depth seems to be an important factor regulating the growth of otoliths in carbonate-saturated levels. The relative growth of the otoliths is usually negatively allometric.     

Sexual dimorphism in the otolith shape of shi drum,Umbrina cirrosa (L.), in the eastern Mediterranean Sea: Fish size–otolith size relationships

Little is known about possible differences in sagitta otolith size and shape between sexes of the shi drum, Umbrina cirrosa, and relationships between their body and otolith size. Thus, this study aimed to fill this knowledge gap via examination of 414 sagittal otoliths from 108 male (total length 13.8–26.8 cm) and 99 female (13.5–26.7 cm) U. cirrosa caught between May 2017 and April 2018 in gillnets set at a depth of ~15 m in Mersin Bay, Eastern Mediterranean Sea. No statistical differences were observed between the shape indices of the left-sided and right-sided sagitta. However, there were significant differences in the size and shape of otoliths between males and females. The slopes of allometric power functions from otolith width × fish sizes gave significant differences between males and females (ANCOVA, P < 0.05). The relationship for length × weight of otoliths from both males and females showed isometric growth, whereas the relationship of otolith width × otolith weight showed positive allometry. Negative allometric growth was observed for the relationship otolith length × otolith width. In summary, this study revealed the presence of sexual dimorphism in the otolith shape of U. cirrosa, and the data on regression relationships of fish-otolith sizes can be used to estimate fish size from U. cirrosa otolith sizes.     

Differential effects of food and temperature lead to decoupling of short-term otolith and somatic growth rates in juvenile King George whiting

In experiments manipulating temperature and food levels, rates of short-term otolith growth and somatic growth of juvenile King George whiting Sillaginodes punctata became decoupled. Food levels were starvation, 100 and 1000 μg per fish per day and temperatures were 12 and 18° C. Short-term somatic growth was influenced predominantly by food, with negligible growth at starvation and low ration, and significant growth at high food ration at both temperatures. In contrast, short-term otolith growth was influenced predominantly by temperature, with significant otolith growth occurring for all food treatments, and elevated otolith growth occurring at the higher temperature across food treatments. The identification of such differential effects of food and temperature leading to decoupling is an important result that has significant implications for using otoliths to estimate short-term growth.     

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 growth of Springer's demoiselle, Chrysiptera springeri (Pomacentridae, Allen & Lubbock), on a protected and non-protected coral reef

The structural complexity of coral reefs is important for their function as shelter and feeding habitats for coral reef fishes, but physical disturbance by human activities often reduce complexity of the reefs by selectively destroying fragile and more complex coral species. The damselfish Springer's demoiselle Chrysiptera springeri primarily utilize complex coral heads for shelter and are hence vulnerable to human disturbance. In order to evaluate the potential effect of habitat degradation on juvenile fish growth, coral reef cover, fish age at settling and otolith growth, juvenile Springer's demoiselle was investigated on a protected and non‐protected coral reef in Darvel Bay, Borneo. The protected reef had higher coverage of complex branching corals and exhibited a more complex 3‐dimensional structure than the non‐protected reef. Springer's demoiselle settled at the same age on non‐protected and protected reefs. The growth rates of the otoliths from Springer's demoiselle were similar during the pre‐settlement period on the two reefs (manova , P > 0.05), but from age 20 to 48 days (post‐settlement period) the otolith growth rate of juveniles on the non‐protected reef was reduced compared to those from the protected reef (manova , P = 0.017). However, the differences in the otolith size, and by inference, fish size, after 48 days were small. The small effect of habitat degradation on growth is likely related to the fact that the Springer's demoiselles collected on the non‐protected reef were associated with the few remaining complex coral heads. Increased foraging‐predation tradeoffs on the non‐protected reef may decrease food intake and growth of juvenile Springer's demoiselle, but the main effect of habitat degradation on their abundance is likely to be related to lack of suitable shelter, and consequently reduced carrying capacity, on disturbed reefs.     

Shifts in drag and swimming potential during grayling ontogenesis: relations with habitat use

The drag coefficient (C_d) of grayling Thymallus thymallus was dependent on body surface conditions and rigidity. At comparable flow conditions, C_d values of a fish preserved in formalin (high body rigidity) were 15–30% lower than those obtained on a freshly-killed fish (medium rigidity); the presence of skin mucus on fish could reduce C_d by 10%. The hydrodynamic potential of grayling increased during ontogenesis, because C_d values decreased (except for yolk sac larvae, which had a particular morphology) and the swimming capacities (in terms of relative muscular mass) increased. Grayling morphology evolves towards hydrodynamically efficient shape at high velocities, and there is a relationship between these shifts in hydrodynamic abilities and the different habitats (in terms of current velocity) used by five morphological groups. Therefore, the concept of hydrodynamic potential (i.e. hydrodynamics of shape and swimming capacities) could be a useful tool in fish ecomorphology and predictions of habitat use.     

Water temperature and fish growth: otoliths predict growth patterns of a marine fish in a changing climate

Ecological modeling shows that even small, gradual changes in body size in a fish population can have large effects on natural mortality, biomass, and catch. However, efforts to model the impact of climate change on fish growth have been hampered by a lack of long‐term (multidecadal) data needed to understand the effects of temperature on growth rates in natural environments. We used a combination of dendrochronology techniques and additive mixed‐effects modeling to examine the sensitivity of growth in a long‐lived (up to 70 years), endemic marine fish, the western blue groper (Achoerodus gouldii), to changes in water temperature. A multi‐decadal biochronology (1952–2003) of growth was constructed from the otoliths of 56 fish collected off the southwestern coast of Western Australia, and we tested for correlations between the mean index chronology and a range of potential environmental drivers. The chronology was significantly correlated with sea surface temperature in the region, but common variance among individuals was low. This suggests that this species has been relatively insensitive to past variations in climate. Growth increment and age data were also used in an additive mixed model to predict otolith growth and body size later this century. Although growth was relatively insensitive to changes in temperature, the model results suggested that a fish aged 20 in 2099 would have an otolith about 10% larger and a body size about 5% larger than a fish aged 20 in 1977. Our study shows that species or populations regarded as relatively insensitive to climate change could still undergo significant changes in growth rate and body size that are likely to have important effects on the productivity and yield of fisheries.     

Qualitative and quantitative models relating otolith zone deposition to growth and condition in sexually mature male and female capelin (Mallotus villosus)

Summary Correspondence analysis (CA) is used to examine the relationship between months, between selected body components/organs and between months and components/organs for male and female capelin from 12 to 37 months of age in Balsfijorden, northern Norway (69°21N:19°06E). The CA profiles have been used to quantify condition with regard to age and season. The major features determining the condition of fish depositing hyaline or opaque otolith zones are itemized using CA, and the data modelled by Multiple Regression (MR) using a cosine curve incorporating the chief mass variables with linear age-dependency. The highest proportion of fish having outer opaque zones are found from ca. June to October, whilst the highest proportion with exterior hyaline zones are found from ca. December to May. There is a clear annual cycle in the deposition of opaque and hyaline otolith zones in both sexes, but there is a significant difference in phase of ca. 12 days between the sexes. There is a significant trend for decreasing proportions of fish having outermost opaque otolith zones with increasing age; this trend is similar in both sexes. The mean level and amplitude of the cycles are similar in both sexes. On the other hand, CA shows a 12-month cycle of storage and utilization of body materials with obvious differences between sexes. In the female protein in the fillet plays a more dominant role than lipid in the fillet in accounting for anabolic and catabolic variations in mass, whereas in the male the opposite is true. Sexual maturation is negatively correlated with fillet (somatic) growth. Variations in stomach weight (with contents) and otolith zone deposition are not significantly correlated. Nevertheless, in both sexes there is a clear positive correlation between stomach weight and liver protein and lipid implying an association between stomach weight and feeding activity. In females, however, maximum liver condition is more positively correlated with exponential ovarian growth, probably through mobilization of lipoproteins for eggs. Qualitative (CA) and quantitative (MR) models have related changes in growth and condition to the type of otolith zone deposited. The fillet of capelin is the major somatic growth site. As CA indicates a negative correlation between fillet reserves and gonad maturation, and the best MR models describing the cycle of otolith zone deposition in males and females (accounting for 93% and 70% respectively of the variation) underlined and quantified the interplay between somatic and gonad growth, it is implicit that the energy balance of the fish will be an important determinant of otolith zone deposition in sexually maturing and mature capelin.