Is the fast growth of an equatorial Micropterus salmoides population explained by high water temperature?

Britton JR, Harper DM, Oyugi DO. Is the fast growth of an equatorial Micropterus salmoides population explained by high water temperature? Ecology of Freshwater Fish 2010: 19: 228–238. © 2010 John Wiley & Sons A/S Abstract – Marginal increment analysis of scales collected from the introduced Micropterus salmoides population of Lake Naivasha, Kenya revealed the formation of an annual growth check, validating their use to age individual fish. Subsequent analysis of scales from 372 fish collected between 2002 and 2009 revealed individuals were very fast growing compared with native populations in North America and other introduced populations in Europe, South America, Africa and Asia. This was likely to be as a result of the water temperatures in Lake Naivasha exceeding 20 °C throughout the year. This was corroborated by a meta‐analysis of the growth parameters asymptotic length L_∞ and growth coefficient K from across their geographical range that revealed variance was explained by differences in mean annual air temperatures. At a break point of approximately 10 °C, there was a shift to reduced L_∞ and increased K, suggesting a temperature driven trade‐off between growth rate and ultimate length. When adjusted for temperature and weighted for sample size, there were significant differences between the growth parameters of the North American and introduced populations, suggesting that other abiotic and biotic variables were also important determinants of the growth of individuals between the two ranges.     

Influences of population density,temperature and latitude on the growth of invasive topmouth gudgeon Pseudorasbora parva

Plasticity in life‐history traits provides advantages for introduced fish in overcoming demographic bottlenecks that would otherwise inhibit establishment. Here, the influence of population density, temperature and latitude was tested on the growth increments and growth rates of invasive populations of topmouth gudgeon Pseudorasbora parva, a small Asian cyprinid fish that is invasive across Europe. Aquaria experiments tested the roles of fish number and temperature on growth increments under a fixed food supply, pond experiments tested the role of density on growth increments, and a field study completed in England and Wales tested the influence of density and latitude on growth rates. In aquaria experiments, whilst growth increments were higher at 21 and 23 °C than at 19 and 25 °C, fish number had a greater influence on growth than temperature. Higher growth increments were produced at lower densities. In experimental ponds, growth increments were significantly higher in ponds with low densities of P. parva compared with those at elevated densities. In the field study comprising 10 wild populations across a latitudinal gradient of 4.0°N, a difference in mean air temperatures of approximately 3 °C, and estimated densities between 0.5 and 65.0 m^?2, population density was the only significant predictor of growth rates. Whilst populations at very low densities comprised of significantly faster growing individuals, there were no significant differences when densities were between 15 and 65 m^?2. Thus, invasive P. parva populations have considerable growth plasticity, especially at low densities, with this likely to be important in their ability to colonise new environments.     

A common environment experiment reveals plastic and genetic contributions to the fast life‐history strategy of an invasive fish

Invasive species often exhibit a suite of life‐history traits that promote rapid population growth, including early age and small size at maturation, and high reproductive investment. The common expression of these “fast” life‐history traits in invasive populations could be the result of plastic and/or genetic responses to the non‐native environment, or in response to the process of range expansion. To determine the relative importance of plastic and genetic contributions to the expression of life‐history traits, we reared two native Canadian and two invasive Spanish populations of Pumpkinseed sunfish (Lepomis gibbosus) in a common environment in central Ontario, Canada. In the wild, European Pumpkinseed tend to exhibit faster juvenile growth rates, younger age and smaller size at maturity, and higher reproductive investment than native North American populations. When reared in a common environment, both native and invasive populations exhibited similar juvenile growth rates, and similar age and size at maturity, suggesting that the differences seen among wild populations are a plastic response to the warmer non‐native environment. However, reproductive investment was consistently higher in the Spanish populations regardless of rearing environment, suggesting a genetic difference in reproductive investment between native and invasive populations. Selection for greater reproductive investment in non‐native Pumpkinseed may have contributed to their widespread success in Europe.     

Effects of exploitation on age, growth and mortality of the blackspot snapper, Lutjanus fulviflamma, at Mafia Island, Tanzania

Abstract Estimates of the growth parameters (L_∞ and K), mortality coefficients (Z, M and F) and exploitation rate (E) for the blackspot snapper, Lutjanus fulviflamma (Forsskål) from the Mafia Island Marine Park (MIMP) and adjacent intensively fished areas in Tanzania were determined. Sectioned otoliths showed that L. fulviflamma in the MIMP attained a maximum age of 18 years, with a high proportion of fish between 6 and 10 years old. The maximum age was 8 years in the intensively fished areas, with a preponderance of 2‐ and 4‐year‐old fish. The size structures of the populations in the MIMP and that in the intensively fished areas were markedly different, with the MIMP fish averaging (±SE) 211.4 ± 0.38 mm TL, but 154.6 ± 0.32 mm TL in the intensively fished areas. The von Bertalanffy growth parameters were L_∞ = 290.3 mm TL, K = 0.15 year^?1 and t₀ = ?2.7 years. There was no significant difference in growth between the four populations (L_∞: F‐stat = 0.14, P = 1.000, and K: F‐stat = 0.26, P = 0.992). Total mortality was 0.55 and 1.64 year^?1 in the MIMP and intensively fished areas, respectively, natural mortality 0.27 year^?1 and fishing mortality 0.18 and 1.37 year^?1 in the MIMP and intensively fished areas, respectively. The exploitation rate was 0.51 and 0.84 in the MIMP and intensively fished areas, respectively. The artisanal seine net fishery is directed mainly at younger fish in the intensively fished areas resulting in growth overfishing. The protracted life span, the slow growth and natural mortality rates imply that L. fulviflamma is vulnerable to overfishing and that the protection provided by the park, although limited, is vital for sustaining the fishery at Mafia Island.     

Scale measurements as a conservation tool in endangered Zingel asper (Linnaeus, 1758)

• 1. Zingel asper (a percid) is a highly endangered endemic fish of the Rhone catchment (France). Scale reading was used to estimate age and growth rates in one of the two last remaining populations that are still present in relatively high densities (River Beaume).
• 2. Scale reading was validated for the first time in Z. asper by comparing back‐calculated lengths from scale annual increment to actual lengths obtained by individual mark–recapture monitoring. The impacts of age or sampling site on individual growth rates were explored using generalized linear models.
• 3. No major discrepancy was observed between actual and back‐calculated lengths. Longevity of Z. asper was inferred from the age data and did not exceed 3 years. Results showed variation in growth rates among ages (20 times higher for 1+ fish than for 2+ or 3+ fish) and also among sampling sites.
• 4. The present work provided the first estimates of annual growth rates in the Beaume population. This study also showed that scale reading allowed a valuable trade‐off between accuracy and conservation imperatives that often imply avoiding invasive techniques such as the implantation of passive integrative transponders.
• 5. Scale reading will be a valuable tool for future ecological studies in Z. asper and will help in developing conservation strategies for this species as longevity and growth patterns are two life‐history traits of major importance for the management of endangered populations.

Copyright © 2007 John Wiley & Sons, Ltd.     

Latitudinal variation in growth and otolith‐inferred field metabolic rates of Canadian young‐of‐the‐year Arctic charr

Countergradient variation (CGV) is defined as genetic variation that counteracts the negative influences of the physical environment, minimising phenotypic variability along an environmental gradient. CGV is thought to have relevance in predicting the response of organisms to climate variability and change. To test the hypothesis that growth rate increased with latitude, consistent with CGV, young‐of‐the‐year (YOY) Arctic charr, Salvelinus alpinus, were examined along a ~27° latitudinal gradient in central and eastern Canada. Growth rates were estimated from fork lengths standardised by the thermal opportunity for growth based on experienced water temperatures derived using otolith oxygen stable isotopes. Results demonstrated patterns consistent with CGV, where northern populations demonstrated faster growth rates. A secondary aim was to test for similar geographical patterns in otolith‐inferred metabolic rates, which reflect the energetic costs of standard metabolic rate (SMR) and other processes such as feeding, locomotion, thermoregulation, reproduction and growth. Results demonstrated a significant, positive relationship between otolith‐inferred metabolic rate and latitude, which may reflect an increase in one, or a combination, of the above‐noted physiological processes. The similar latitudinal pattern in growth and otolith‐inferred metabolic rates suggests greater intake of food per unit of time by northern fish. The phenotypic variation in physiological traits observed here demonstrates the significant adaptability of Arctic charr to different thermal regimes with different growing season lengths. Determining the relative contributions of phenotypic plasticity and genetic variation to the observed latitudinal variation will be critical to predicting the responses of Arctic charr to climate change more accurately.     

Fitting growth with the von Bertalanffy growth function: a comparison of three approaches of multivariate analysis of fish growth in aquaculture experiments

Three approaches for multivariate analysis of fish growth in aquaculture experiments with Nile tilapia (Oreochromis niloticus niloticus L.) based on the von Bertalanffy growth curve are presented and compared. The approaches are: an extended Gulland‐and‐Holt (GH) plot, a forced extended GH plot and a multilinear regression analysis for the growth parameter K. All three models provide valuable insight into the major environmental factors influencing the daily growth rate and explain 28–46% of the variance of the observed daily growth rate of the used data set. For all three methods, the modelled parameter is significantly related to the net yield of Nile tilapia and can, therefore, be used for the predictive modelling of management scenarios. The extended GH plot loads the influence of environmental parameters upon L_∞, while the forced extended GH plot and Direct fitting of K load the influence on the growth parameter K. The latter is more in the tradition of aquaculture research. But the forced extended GH plot and Direct fitting of K can only be applied if L_∞ of the cultured species is known, as the selected L_∞ influences the variance in the regression variables.     

Inter‐ and intra‐individual variability in growth and food consumption in pikeperch,Sander lucioperca L., larvae revealed by individual rearing

We examined short‐term, inter‐ and intra‐individual variability in rates of growth and food consumption in fish early life stages to gain a mechanistic understanding of why larvae in the same environments often grow at vastly different rates. We made parallel measurements of growth rate in standard length (GR_SL) and food consumption rate (C), and provide estimates of weight growth rate (GR_DW) and gross growth efficiency (GGE = 100*GR_DW/C) of individually reared larvae of pikeperch, Sander lucioperca L., fed Artemia nauplii at 20°C and a salinity of 2.0 g L^?1. Within two trials, GR_SL, C and GGE were obtained for 108 larvae over a maximum period of 28 days. Mean (±SD) initial size, GR_SL, C and GGE were 19.49 (9.19) mm, 0.68 (0.21) mm day^?1, 0.85 (0.44) mg day^?1 and 36.5 (10.2)% respectively. The vast majority (91%) of the variability in growth was explained by differences in food consumption. When isolated from conspecifics for 28 days, relatively small larvae grew faster than relatively large ones, partially mitigating initial differences in size‐at‐age.     

Gills,growth and activity across fishes

Life history theory suggests that maximum size and growth evolve to maximize fitness. In contrast, the Gill Oxygen Limitation Theory (GOLT) suggests that growth and maximum size in fishes and other aquatic, water-breathing organisms is constrained by the body mass-scaling of gill surface area. Here, we use new data and a novel phylogenetic Bayesian multilevel modelling framework to test this idea by asking the three questions posed by the GOLT regarding maximum size, growth and gills. Across fishes, we ask whether the body mass-scaling of gill surface area explains (1) variation in the von Bertalanffy growth coefficient (k) above and beyond that explained by asymptomatic size (W_∞), (2) variation in growth performance (a trait that integrates the tradeoff between k and W_∞) and (3) more variation in growth performance compared to activity (as approximated by caudal fin aspect ratio). Overall, we find that there is only a weak relationship among maximum size, growth and gill surface area across species. Indeed, the body mass-scaling of gill surface area does not explain much variation in k (especially for those species that reach the same W_∞) or growth performance. Activity explained three to five times more variation in growth performance compared to gill surface area. Our results suggest that in fishes, gill surface area is not the only factor that explains variation in maximum size and growth, and that other covariates (e.g. activity) are likely important in understanding how growth, maximum size and other life history traits vary across species.     

Modelling individual variability in growth of bull trout in the Walla Walla River Basin using a hierarchical von Bertalanffy growth model

We examined growth in length of fluvial bull trout (Salvelinus confluentus) in the Walla Walla River Basin, Washington and Oregon. Our objectives were to quantify individual variability in growth; examine growth within and among years, life history forms, life stages and sexes; and estimate von Bertalanffy growth parameters. Individual variability was evaluated by modelling asymptotic length (L_∞) and the growth coefficient (k) as random variables. All models were fit with Bayesian methods and were evaluated for fit by the deviance information criterion. By incorporating individual variability, population‐level estimates of L_∞ and k appeared appropriate and estimated growth trajectories for specific bull trout fit individual observed patterns in growth. Growth trajectories and positive correlation between individual estimates of L_∞ and k suggest that some individuals grow at a faster rate and reach a larger maximum size than other individuals and those differences are maintained throughout life. Selected models suggest that fluvial migrants have higher estimates of L_∞ and k than residents, but there were only slight differences in parameter estimates among migrants from two adjacent spawning populations in the Walla Walla River Basin, as well as between males and females. Growth rates increased for fluvial migrants after subadult emigration. Individual variability in growth is consistent with the life history diversity assumed essential for bull trout population persistence. Quantifying this variability is important for modelling population dynamics and viability to conserve this threatened species.     

Growth of common carp Cyprinus carpio in Anatolia (Turkey), with a comparison to native and invasive areas worldwide

Common carp Cyprinus carpio occurs in several non‐native areas worldwide, where it is generally regarded as either naturalised or invasive. Anatolia (Turkey) represents a unique region for evaluating common carp growth, due both to its location at the southernmost range of expansion of the species' wild form and to most of its water bodies having been stocked with domesticated strains. Based on a review of length‐at‐age data for common carp stocks from 45 water bodies sampled between 1953 and 2007, regional patterns in growth across climates, water body types, scalation variants and sexes, along with altitudinal gradients in growth performance and mortality, were investigated. Growth rates were lower in cold and arid relative to temperate climates, and also under hot or dry summers; this was true also of the mirror relative to the scale variant, males to females, but not of water body types (i.e., man‐made reservoirs, natural lakes, water courses). Growth performance and mortality decreased with increasing altitude and decreasing temperature, likely due to optimisation of resource allocation between growth and reproduction. Growth rate of common carp from Anatolia was consistently lower compared to its native (Eurasian) and, especially, invasive (North American) counterparts, which reflected an opportunistic life‐history strategy. Lower growth rates in Anatolia were ascribed to lower resilience of the widespread mirror variant together with limited habitat for spawning in man‐made reservoirs. Better knowledge of common carp growth in Anatolia will improve stock management and conservation efforts. Further studies will help clarify the mechanisms responsible for evolutionary genotype–phenotype inter‐relationships.     

Spatial variation in the somatic growth rates of European barbel Barbus barbus: a UK perspective

The European barbel Barbus barbus is threatened in areas of its range because of its sensitivity to anthropogenic disturbance in riverine habitats and, in the UK, is indigenous to a relatively small number of east‐flowing rivers, with nonindigenous populations present in other rivers following introductions for angling enhancement. Fish stock assessment surveys completed between 2002 and 2010 collated age and growth data from 20 rivers across their indigenous and nonindigenous UK range. Analyses revealed that individuals present in samples are of 21 years old, with growth rates highly variable between rivers. There was no relationship between growth rates and the maximum age of fish per river, and there was no difference in growth rates between their indigenous and nonindigenous ranges. A range of abiotic data were collated and analysed against the growth data; these analyses suggested higher mean growth rates were evident in rivers of higher biological water quality (expressed as British Monitoring Working Party Score) and higher mean air temperatures (used as a surrogate of water temperature). That growth of B. barbus was significantly and positively enhanced by increased biological water quality was in contrast to cyprinid fishes such as roach Rutilus rutilus and suggests that as river water quality continues to improve through reduced nutrient inputs, further ecological changes are likely in riverine fish communities.     

Age and growth rates of the critically endangered fish Garra ghorensis can inform their conservation management

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Decreasing shrimp (Pandalus borealis) sizes off Newfoundland and Labrador – environment or fishing?

During the 1990s, carapace length statistics including minimum size caught (L_min), mean male and female lengths, size at sex transition (L₅₀) and maximum size (L_max) of northern shrimp (Pandalus borealis) decreased in commercial and survey catches off Newfoundland and Labrador. Decreased growth rates caused by decreases in per‐capita food availability due to large population increases, exacerbated by increased metabolic demands from higher water temperatures in the mid‐1990s, appear to be the main cause of the size decrease. Fishing could have had an accelerating effect on environmentally driven decreases in shrimp growth and size by ‘cropping’ the largest shrimp from the population. The greatest decreases in shrimp size occurred in Hudson Strait and the adjacent northern shelf, the area which also has the highest densities and largest shrimp. We hypothesize that the greater size decrease here resulted from decreased primary production from decreased nutrient flux into the euphotic zone, caused by increased atmospheric warming, freshwater runoff and stratification during the warming trend of the 1990s.     

Polyculture of milkfish Chanos chanos (Forsskal) and the red seaweed Gracilariopsis bailinae (Zhang et Xia) in brackish water earthen ponds

Growth, net production, and survival rates of milkfish cultured with Gracilariopsis bailinae at two stocking density combinations (T₁– 30 fingerlings 100‐m^?2 pond+1‐kg G. bailinae 4‐m^?2 net cage, T₂– 30 fingerlings 100‐m^?2 pond+2‐kg G. bailinae 4‐m^?2 net cage) in brackish water earthen ponds over four culture periods were determined. The control (T₃) was stocked at 30 fingerlings 100‐m^?2 pond. Specific growth and production rates of G. bailinae were also calculated. There were no significant differences in mean growth, survival, and net production rates of milkfish between the three treatments. Irrespective of stocking singly or in combination with G. bailinae, significantly higher mean growth and mean production rates for milkfish were obtained during the third culture period of year 1 than those obtained from the other culture periods. Survival rates were not significantly different among the four culture periods. There were no significant differences in mean specific growth and mean net production rates between the two stocking densities of G. bailinae. Significantly higher mean specific growth and mean net production rates of red seaweed were also obtained during the third culture period of year 1 than those obtained from other culture periods. The production of milkfish and red seaweed was higher during the dry season. Growth rates of milkfish was positively correlated with temperature and salinity, while net production rates were positively correlated with temperature and total rainfall, but was inversely correlated with dissolved oxygen. G. bailinae growth and net production rates were positively correlated with water temperature and salinity. Results show that milkfish can be polycultured with G. bailinae grown in net cages in brackish water ponds at stocking density combination of 30 fingerlings 100‐m^?2 pond+1‐kg G. bailinae 4‐m^?2 net cage.     

Square‐mesh codend length and selectivity in southeastern Australian stow nets

Abstract The relationship between the amount of square mesh in codends and selectivity was investigated for an Australian penaeid stow‐net fishery. Three lengths (3, 2 and 1 m) of square‐mesh codend made from 27‐mm mesh hung on the bar were alternately tested with a conventional 34‐mm diamond‐mesh design during two covered‐codend experiments. Compared with the conventional codend, the square‐mesh configurations incrementally selected school prawns, Metapenaeus macleayi (Haswell) across narrower selection ranges (SR) and mostly at greater sizes at 50% retention (L₅₀), while retaining fewer fish. Irrespective of the mesh configuration or square‐mesh codend length, there were significant differences between experiments (attributed to water flow) and impacts of catch weight on the selectivity of school prawns. Both variables had a negative relationship with L₅₀, while water flow similarly affected SR. This study reaffirms the utility of square‐mesh codends as a key input control for managing the selectivity of penaeid‐catching gears.     

Size structure,not metabolic scaling rules,determines fisheries reference points

Impact assessments of fishing on a stock require parameterization of vital rates: growth, mortality and recruitment. For ‘data‐poor’ stocks, vital rates may be estimated from empirical size‐based relationships or from life‐history invariants. However, a theoretical framework to synthesize these empirical relations is lacking. Here, we combine life‐history invariants, metabolic scaling and size‐spectrum theory to develop a general size‐ and trait‐based theory for demography and recruitment of exploited fish stocks. Important concepts are physiological or metabolic scaled mortalities and flux of individuals or their biomass to size. The theory is based on classic metabolic relations at the individual level and uses asymptotic size W_∞ as a trait. The theory predicts fundamental similarities and differences between small and large species in vital rates and response to fishing. The central result is that larger species have a higher egg production per recruit than small species. This means that density dependence is stronger for large than for small species and has the consequence that fisheries reference points that incorporate recruitment do not obey metabolic scaling rules. This result implies that even though small species have a higher productivity than large species their resilience towards fishing is lower than expected from metabolic scaling rules. Further, we show that the fishing mortality leading to maximum yield per recruit is an ill‐suited reference point. The theory can be used to generalize the impact of fishing across species and for making demographic and evolutionary impact assessments of fishing, particularly in data‐poor situations.     

Temperature influences on growth of unfished juvenile Northern cod (Gadus morhua) during stock collapse

This study examined growth of unfished juvenile Northern cod (Gadus morhua) off Newfoundland concomitant with stock collapse in the cold early 1990s. Two unpublished data sets were examined, one from collapse‐period trapping sites along the northeast coast of Newfoundland and one from a post‐collapse inshore trawl survey. Cumulative surface and bottom temperatures were significant predictors of growth rates of the young fish with year‐classes born during collapse experiencing slower growth than those born during subsequent warming. Relationships between accrued temperature and growth were consistent across periods, with slow growth of collapse‐period fish reflecting slower accumulation of temperature‐at‐age. Temperature influences were spatially broad‐based with no significant differences in growth rates for fish captured along the entire northeast coast of Newfoundland. Predicted differences in growth rates for collapse versus recovery year‐classes were proportional to cumulative surface temperatures but not cumulative bottom temperatures. Although significant, temperature effects on growth were relatively unimportant at youngest ages. Overall, growth differences between periods were small but large differences occurred between slowest and fastest growing year‐classes. The results suggest initial responses to increasing temperatures were delayed following collapse. We conclude that although temperature was an important determinant of dampened productivity that it alone cannot account for the collapse and slow recovery of the stock. This is the first known study to directly quantitatively link temperature impacts to an unfished component of the Northern cod stock complex during collapse, removing need for implicit assumptions about whether or not cold conditions contributed to the collapse of this iconic fish stock.     

Effects of temperature and food availability on growth rate during late larval stage of Japanese anchovy (Engraulis japonicus) in the Kuroshio–Oyashio transition region

During periods when the population size of Japanese anchovy Engraulis japonicus is large, the abundance of 1‐yr olds has been considered to be dependent on the growth and survival processes in the late larval and early juvenile stages in the Kuroshio–Oyashio transition region off northern Japan. Recent growth rates for 10 days before capture of larval and early juvenile E. japonicus were estimated and examined in relation to the surface water temperature and the available copepod density in 1997, 1998 and 1999. Late larval and early juvenile E. japonicus were distributed in the waters with temperature from 15 to 19°C and available prey density from 10 to 1000 mg dry weight (DW) m^?2 in the transition region. The late larval growth rates were found to be regulated more strongly by water temperature than by copepod density in the waters <16°C, and more strongly by copepod density than water temperature in the waters <100 mg DW m^?2 in the Kuroshio–Oyashio transition region. The recent growth rates decreased from the western waters to the eastern waters in the survey area 140–170°E in 1998, correlating with decreases of food availability to 50–100 mg DW m^?2. While in 1999, the recent growth rates were faster in the waters east of 150°E, resulting from eastward expansion of warm water ranges and high available prey density 100–400 mg DW m^?2. The key environmental factors regulating late larval growth rate of E. japonicus in the transition region seem to be spatially different between years.     

Evolutionary assembly rules for fish life histories

We revisit the empirical equation of Gislason et al. (2010, Fish and Fisheries 11 :149–158) for predicting natural mortality (M, year^?1) of marine fish. We show it to be equivalent to , where L_∞ (cm) and K (year^?1) are the von Bertalanffy growth equation (VBGE) parameters, and L (cm) is fish length along the growth trajectory within the species. We then interpret K in terms of the VBGE in mass , and show that the previous equation is itself equivalent to a ?? power function rule between M and the mass at first reproduction (W_α); this new ?? power function emerges directly from the life history that maximizes Darwinian fitness in non‐growing populations. We merge this M, W_α power function with other power functions to produce general across‐species scaling rules for yearly reproductive allocation, reproductive effort and age at first reproduction in fish. We then suggest a new way to classify habitats (or lifestyles) as to the life histories they should contain, and we contrast our scheme with the widely used Winemiller–Rose fish lifestyle classification.