The effect of growth rate on otolith-based discrimination of cod (Gadus morhua) ecotypes

Otolith shape has previously been used to identify ecotypes within the Icelandic cod (Gadus morhua) stock, using DST profiles to validate the results. Fish otolith shape variation has repeatedly been found to be largely determined by growth rate. To examine the effect of growth rate on the relationship between otolith shape and cod ecotypes (using the Pan I genotype as a proxy for ecotype), 826 archived sagittal otoliths collected over a 58 year sampling period were retrieved, the individual growth rate calculated, and otolith shape described using both Normalized Elliptic Fourier transform and Discrete Wavelet transform. Discriminant functions of otolith shape successfully classified ecotype, whether using Fourier or Wavelet descriptors, but only when excluding a heterozygous genotype from the analysis. The otolith shape variability of this genotype lowered the classification success, while otolith shape, in turn, was significantly affected by growth rate and cohort. Growth rate differences previously reported for the ecotypes were present, but were less marked than expected and indeed, growth rate variance attributable to ecotype identity was dwarfed by cohort- and location-related variance in growth. Such a strong effect of growth rate suggests that cod ecotype discrimination based on otolith shape is sensitive to both temporal and spatial variations in growth, which can mask the effect of ecotype-related growth rate differences on otolith shape.

Applications

By affecting age-specific survival and fecundity, human-induced disturbances affect life history. This has potential to affect r max with negative consequences for species viability and persistence. Several types of assessments are used to classify vulnerability to extinction, exploitation, and climate change. When information on r max is unavailable, vulnerability assessments often rely on life-history correlates of r max. These have included generation time, age at maturity, maximum size, longevity, fecundity, natural mortality, and individual growth rate. Empirical research indicates that links with r max are strong for some traits, such as age at maturity and body size, but weak for others, such as fecundity. In addition to assessments of declining species, efforts have been made to identify life-history correlates of the rate and uncertainty in species recovery. Persistence and stability can be strengthened by the magnitude of life-history variation. The greater the variability in life history within and among, the greater the resistance and resilience of populations and species.

The regulating effect of growth plasticity on the dynamics of structured populations

Plasticity is the extent to which life history processes such as growth and reproduction depend on the environment. Plasticity in individual growth varies widely between taxa. Nonetheless, little is known about the effect of plasticity in individual growth on the ecological dynamics of populations. In this article we analyse a physiologically structured population model of a consumer population in which the individual growth rate can be varied between entirely plastic to entirely non-plastic. We derive this population level model from a dynamic energy budget model to ensure an accurate energetic coupling between ingestion, somatic maintenance, growth, and reproduction within an individual. We show that the consumer population is either limited by adult fecundity or juvenile survival up to maturation, depending on the level of growth plasticity and the non-plastic individual growth rate. Under these two regimes we also find two different types of population cycles which again arise due to fluctuation in respectively juvenile growth rate or adult fecundity. In the end our model not only provides insight into the effects of growth plasticity on population dynamics, but also provides a link between the dynamics found in age- and size-structured models.

Otolith-based discrimination of cod ecotypes and the effect of growth rate

Otolith shape has previously been used to identify ecotypes within the Icelandic cod (Gadus morhua) stock, using DST profiles to validate the results. Fish otolith shape variation has repeatedly been found to be largely determined by growth rate. To examine the effect of growth rate on the relationship between otolith shape and cod ecotypes (using the Pan I genotype as a proxy for ecotype), 826 archived sagittal otoliths collected over a 52 year sampling period were retrieved, the individual growth rate calculated, and otolith shape described using both Normalized Elliptic Fourier transform and Discrete Wavelet transform. Discriminant functions of otolith shape yielded high ecotype classification success, whether using Fourier or Wavelet descriptors, but only when excluding a heterozygous genotype from the analysis. The otolith shape variability of this genotype lowered the classification success, while otolith shape, in turn, was significantly affected by growth rate and cohort. Growth rate differences previously reported for the ecotypes were present, but were less marked than expected and indeed, growth rate variance attributable to ecotype identity was dwarfed by cohort- and location-related variance in growth. Such a strong effect of growth rate suggests that cod ecotype discrimination based on otolith shape is sensitive to both temporal and spatial variations in growth, which can mask the effect of ecotype-related growth rate differences on otolith shape.

Growth and biological characteristics of pike perch Sander lucioperca (Linnaeus, 1758) in the Amur River

Linear and weight growth of pike perch in the Amur River estuary is considered using the data on age determined for 197 specimens. The growth is described by von Bertalanffy and Schmalhausen equations. Some biological parameters of pike perch as the maximum size, age of mass maturation, etc. are calculated using the age-differentiated coefficients of natural mortality. The growth and biological parameters of pike perch in the Amur estuary are compared with the same parameters of this species in the Amur River at Khabarovsk. Recently 3 ecological forms of pike perch are distinguished in the Amur basin: i) riverine ecotype self-redistributed from Lake Khanka, ii) lacustrine ecotype in the lower Amur River, and iii) highly productive semi-anadromous marime ecotype in the Amur estuary. The 3rd phase of pike perch acclimatization is observed now in the Amur estuary known as the «bloom» phase accompanied with prominent increasing of population abundance and individual growth rate acceleration. Pike perch prey in this area mainly on juveniles of non-anadromous and diadromous fish, or on pond smelt Hypomesus olidus during their concentration in the estuary in winter.

Intact rather than total circulating insulin-like growth factor binding protein-1a is a negative indicator of growth in masu salmon

Insulin-like growth factor binding protein (IGFBP)-1a is one of three major circulating forms in salmon and induced under catabolic conditions. However, there is currently no immunoassay available for this form because of a lack of standard and specific antibodies. We developed a time-resolved fluoroimmunoassay (TR-FIA) for salmon IGFBP-1a using recombinant protein for labeling, an assay standard, and production of antiserum. The TR-FIA had a low cross-reactivity (3.6%) with IGFBP-1b, another major form in the circulation. Fasting for 4 wk had no effect on serum immunoreactive (total) IGFBP-1a levels in yearling masu salmon, whereas 6-wk fasting significantly increased it. There was a significant, but weak, negative relationship between serum total IGFBP-1a level and individual growth rate ( r2 = 0.12, P = 0.01). We next developed a ligand immuno-functional assay (LIFA) using europium-labeled IGF-I to quantify intact IGFBP-1a. In contrast to total IGFBP-1a, serum intact IGFBP-1a levels increased after 4 wk of fasting, and refeeding for 2 wk restored it to levels similar to those of the fed control. Serum intact IGFBP-1a levels showed a significant negative correlation with individual growth rate ( r2 = 0.52, P < 0.001), which was as good as that of IGFBP-1b. Our findings using newly developed TR-FIA and LIFA suggest that regulation of intact IGFBP-1a levels has an important effect on growth in salmon and that intact IGFBP-1a is a negative index of salmon growth.

Age validation of juvenile cod in the Western Baltic Sea

The methods routinely used to estimate fish age are often un-validated and susceptible to errors and uncertainties. Despite numerous attempts, age determination of western Baltic cod (WBC, Gadus morhua) using otoliths is still unreliable, predominantly due to inconsistent interpretation of the first translucent zone (TZ). Length-frequencies of undersized (&lt;38 cm) cod collected during 2013–2016 from pound nets near Fehmarn Island were analysed to understand TZ formation patterns. A clear minimum separated two cohorts within the length-frequency samples every year. The length-frequency information was combined with otolith edge analysis to observe the development of TZs in age-0 and age-1 cod otoliths, and to validate the timing of TZ formation, which was consistently completed between September and December. Mean TZ diameters of 4 917 juvenile cod otoliths varied between cohorts (mean diameters of the first TZ: 2.0 ± 0.5 mm; second TZ: 3.9 mm ± 0.5) and TZ diameter variation was found to be related to individual growth rate. The timing of formation of the first TZ was positively related to water temperature, and was confirmed as a “summer ring” rather than a “winter ring”. TZ formation and shallow-water occupancy suggest an influence of peak summer water temperatures on WBC ecology. An age reading guide for juvenile WBC otoliths is provided.