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The spawning potential ratio (SPR) is a well-established biological reference point, and estimates of SPR could be used to inform management decisions for data-poor fisheries. Simulations were used to investigate the utility of the length-based model (LB-SPR) developed in Hordyk et al. (2015). Some explorations of the life history ratios to describe length composition, spawning-per-recruit, and the spawning potential ratio. ICES Journal of Marine Science, 72: 204–216.) to estimate the SPR of a stock directly from the size composition of the catch. This was done by (i) testing some of the main assumptions of the LB-SPR model, including recruitment variability and dome-shaped selectivity, (ii) examining the sensitivity of the model to error in the input parameters, and (iii) completing an initial empirical test for the LB-SPR model by applying it to data from a well-studied species. The method uses maximum likelihood methods to find the values of relative fishing mortality (F/M) and selectivity-at-length that minimize the difference between the observed and the expected length composition of the catch, and calculates the resulting SPR. When parameterized with the correct input parameters, the LB-SPR model returned accurate estimates of F/M and SPR. With high variability in annual recruitment, the estimates of SPR became increasingly unreliable. The usefulness of the LB-SPR method was tested empirically by comparing the results predicted by the method with those for a well-described species with known length and age composition data. The results from this comparison suggest that the LB-SPR method has potential to provide a tool for the cost-effective assessment of data-poor fisheries. However, the model is sensitive to non-equilibrium dynamics, and requires accurate estimates of the three parameters (M/k, L∞, and CVL∞). Care must be taken to evaluate the validity of the assumptions and the biological parameters when the model is applied to data-poor fisheries.

We investigated the effects of acid washing on the carbon and nitrogen composition and stable isotope ratios of C and N in shrimp (Metapenaeus spp.) and seagrass (Enhalus acoroides). Acid washing did not affect the mean δ13C ratios for juvenile Metapenaeus moyebi and resulted in only an ecologically insignificant change (0.3‰) in mean δ13C ratios for larger Metapenaeus bennettae. In contrast, acid washing increased the mean δ15N signatures of shrimp tissue (∼ 3‰) and decreased that of seagrass (∼1.8‰) to a degree that may confound the interpretation of food webs. The increase in %C and %N in both shrimp and seagrass after acid washing suggests that the changes in isotope ratios are due to loss of molecules comparatively low in C and N. Treating samples by acid washing also resulted in an increase in the variation among individuals for both δ15N and δ13C, which would lead to a loss of statistical power for testing differences between species, sites, or seasons.

River discharge has long been recognized as one of the factors that contributes to the high productivity of estuaries. Although there is little evidence that river inputs of terrestrial carbon make a direct contribution to coastal food webs, such exported nutrients may stimulate in situ production in estuaries and thus enhance the survivorship and growth of fish and crustaceans in these systems. Furthermore, fluctuations in salinity and turbidity may influence the extent of available habitat for fish and crustaceans and therefore their distribution and/or catchability. Despite these potential links between flow and the secondary production of estuaries and coastal waters, there is still a common perception that 'water going to sea is wasted' and a continuing trend to regulate the flow of rivers. We review the evidence for links between river flow and the productivity of estuarine/coastal fisheries, drawing on a case study of the Logan River in southeast Queensland, and explore the potential mechanisms for these linkages. Our research, and that of others, confirms that high river discharge can have a strong positive effect on the production of commercial and recreational coastal fisheries. It also shows that the seasonal pattern of flow is equally, if not more important, than the magnitude of flow. River regulation is likely to have a dramatic effect on the production of coastal fisheries and, given the current pressures for water resource development, this is an important avenue for future research and evaluation.

The complexity and cost of assessment techniques prohibits their application to 90% of fisheries. Simple generic approaches are needed for the world's small-scale and data-poor fisheries. This meta-analysis of the relationship between spawning potential and the normalized size and age of 123 marine species suggests that the so-called Beverton–Holt life-history invariants (BH-LHI; Lm/L∞, M/k, M × Agem) actually vary together in relation to life-history strategy, determining the relationship between size, age, and reproductive potential for each species. Although little realized, the common assumption of unique values for the BH-LHI also implies that all species share the same relationship between size, age, and reproductive potential. This implicit assumption is not supported by this meta-analysis, which suggests that there is considerable but predictable natural variation in the BH-LHI ratios and the relationships between size, age, and reproductive potential that they determine. We believe that this reconceptualization of the BH-LHI has potential to provide a theoretical framework for “borrowing” knowledge from well-studied species to apply to related, unstudied species and populations, and when applied together with the assessment technique described by Hordyk et al. (2015b), could make simple forms of size-based assessment possible for many currently unassessable fish stocks.

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Evaluating the status of data-poor fish stocks is often limited by incomplete knowledge of the basic life history parameters: the natural mortality rate (M), the von Bertalanffy growth parameters (L∞ and k), and the length at maturity (Lm). A common approach to estimate these individual parameters has been to use the Beverton–Holt life history invariants, the ratios M/k and Lm/L∞, especially for estimating M. In this study, we assumed no knowledge of the individual parameters, and explored how the information on life history strategy contained in these ratios can be applied to assessing data-poor stocks. We developed analytical models to develop a relationship between M/k and the von Bertalanffy growth curve, and demonstrate the link between the life history ratios and yield- and spawning-per-recruit. We further developed the previously recognized relationship between M/k and yield- and spawning-per-recruit by using information on Lm/L∞, knife-edge selectivity (Lc/L∞), and the ratio of fishing to natural mortality (F/M), to demonstrate the link between an exploited stock's expected length composition, and its spawning potential ratio (SPR), an internationally recognized measurement of stock status. Variation in length-at-age and logistic selectivity patterns were incorporated in the model to demonstrate how SPR can be calculated from the observed size composition of the catch; an advance which has potential as a cost-effective method for assessing data-poor stocks. A companion paper investigates the effects of deviations in the main assumptions of the model on the application of the analytical models developed in this study as a cost-effective method for stock assessment [Hordyk, A. R., Ono, K., Valencia, S., Loneragan, N. R., and Prince, J. D. 2015. A novel length based empirical estimation method of spawning potential ratio (SPR), and tests of its performance, for small-scale, data-poor fisheries. ICES Journal of Marine Science, 72: 217–231].