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Feed-food competition is the allocation of resources that can be used to feed humans to animal feed instead, a current but unsustainable practise not well documented for aquaculture. Here, we analysed feed-food competition in aquaculture using two measures; natural trophic levels (TLs) and species-specific human-edible protein conversion ratios (HePCRs).The HePCR equals the ratio of human edible protein in feed (input) to the human edible protein in animal produce (output). To provide prospects on aquaculture's potential to convert human inedible by-products into edible biomass, data on aquaculture production were collected and categorized based on natural TLs. HePCRs were computed for four aquaculture species produced in intensive aquaculture systems: Atlantic salmon, common carp, Nile tilapia and whiteleg shrimp. Under current feed use, we estimated that the carp, tilapia and shrimp considered were net contributors of protein by requiring $0.6 kg of human edible protein to produce 1 kg of protein in the fillet/meat. Considering soya bean meal and fishmeal as food-competing ingredients increased the HePCR to $2 and turned all of the casestudy species into net consumers of protein. To prevent this increase, the use of highquality food-competing ingredients such as fishmeal, or soya bean products should be minimized in aquaculture feed. In the future, the role of aquaculture in circular food systems will most likely consist of a balanced mix of species at different TLs and from different aquaculture systems, depending on the by-products available.

The additive genetic response per generation and the genetic superiority of female genotype(s) selected for commercial cloning (clonal response) were maximized for a closed adult nucleus scheme, with 256 or 1024 test places, by varying the mating design (number of clones, full-sibs and half-sibs). Responses were corrected for effects of finite sample size and correlated index values on the selection intensity, and variance reduction due to selection. Additive genetic responses, which varied from 0-153 to 0-514 phenotypic standard deviations per generation, were 0-68 to 0-89 of corresponding uncorrected predictions. Reductions were largest when the intensity and accuracy of male selection were high. Clonal responses varied from 0-460 to 2-506 phenotypic standard deviations, increasing with the intra-clone correlation, the intensity of clonal selection and the test capacity. Reductions in clonal responses, which varied from proportionally 0-04 to 0-27, were smallest when dominance variance was high. Increasing the test capacity resulted in a proportionally 0-21 to 1-55 increase in genetic responses, while proportional increases in clonal responses varied from 0-09 to 0-36. With selection of only one male per full-sib family, designs which maximized genetic and clonal responses were different in all cases. Differences were largest when the heritability and the intra-clone correlation were low and the intensity of clonal selection was high. Without the restriction on male selection, optimal mating designs were different, unless dominance variance and intensity of clonal selection were both low.

Designs testing clones in a closed nucleus, in which 1024 cows are tested each year, were compared for their additive genetic response to selection (genetic response) and their genetic superiority of female genotype(s) selected for commercial cloning (clonal response), using stochastic simulation. Clones were tested at the expense of dam or sire families, matings per dam (sire), or full-sibs per family. The reference design maximized the genetic response corrected for inbreeding in the absence of cloning. The trait considered was overall economic merit for milk production, which was simulated assuming an approximate infinitesimal model with both additive and dominant gene action. Bulls and cows eligible for breeding were selected on their animal model estimated additive genetic effect at either 15 or 27 months of age. Female genotypes eligible for commercial cloning were selected on their estimated total genetic effect at 27 months of age. All (fe)male full-sibs were available for selection. With only additive gene action, testing clones at the expense of sire families, matings per dam or full-sibs per family reduced genetic response, while it increased clonal response and inbreeding. Testing clones at the expense of dam families, however, added to both the genetic and clonal response without increasing inbreeding. When eight clones were tested at the expense of dam families, the genetic response and the final genetic level of commercially available cloned embryos were maximal. Accuracy of clonal selection equalled 0·83. With dominant gene action, however, testing two clones at the expense of dam families maximized the final genetic level of cloned embryos, irrespective of the level of inbreeding depression (accuracy of 0·72). Reliable commercial clone lines can be produced now and in future generations by testing clones at the expense of dam families.

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