Native seed underpins the success of most terrestrial restoration efforts globally; however, the fragility of the native seed supply chain presents a key challenge to achieving global restoration goals. With the current heightened global focus on ecological restoration, seed supply chains are under unprecedented pressure worldwide. New and practical solutions are required to help the native seed industry move toward more sustainable and reliable supply, and in turn, facilitate more cost-effective, successful, seed-based restoration. Here we focus on species used in biodiverse mine site restoration in two regions of Western Australia as a test case for evaluating two key elements of the seed supply chain: seed quality and price. The study assessed seed quality in 185 species, then combined these results with seed price to determine the actual cost of pure live seeds (PLS) used in restoration. Average seed quality, expressed as a weight percentage of PLS, is 55%. The average price for a native seed batch across 129 species is $1,093 Australian dollars (AUD)/kg, and when adjusted for viability and purity is $2,600 (AUD)/ kg of PLS. We suggest replacing the traditional approach of pricing seed per unit weight ($/kg) with a new method that would reflect seed quality and unit number; price per thousand pure live seeds ($ TPLS). We posit that this new way of pricing native seeds would increase transparency and information flow in the marketing of native seeds, which will, in turn, enable seed users to more reliably plan for, and evaluate the cost-effectiveness of seed-based restoration projects.

1. Global interest in building healthy soils combined with new DNA sequencing technologies has led to the generation of a vast amount of soil microbial community (SMC) data. 2. SMC analysis is being adopted widely for monitoring ecological restoration trajectories. However, despite the large and growing quantity of soil microbial data, it remains unclear how these data inform and best guide restoration practice. 3. Here, we examine assumptions around SMC as a tool for guiding ecosystem restoration and evaluate the effectiveness of using species inventories of SMC as a benchmark for restoration success. 4. We investigate other approaches of assessing soil health, and conclude that we can significantly enhance the utility of species inventory data for ecological restoration by complementing it with the use of non-molecular approaches.

Substantial climate changes are evident across Australia, with declining rainfall and rising temperature in conjunction with frequent fires. Considerable species loss and range contractions have been predicted; however, our understanding of how genetic variation may promote adaptation in response to climate change remains uncertain. Here we characterized candidate genes associated with rainfall gradients, temperatures, and fire intervals through environmental association analysis. We found that overall population adaptive genetic variation was significantly affected by shortened fire intervals, whereas declining rainfall and rising temperature did not have a detectable influence. Candidate SNPs associated with rainfall and high temperature were diverse, whereas SNPs associated with specific fire intervals were mainly fixed in one allele. Gene annotation further revealed four genes with functions in stress tolerance, the regulation of stomatal opening and closure, energy use, and morphogenesis with adaptation to climate and fire intervals. B. attenuata may tolerate further changes in rainfall and temperature through evolutionary adaptations based on their adaptive genetic variation. However, the capacity to survive future climate change may be compromised by changes in the fire regime.

Trait divergence between populations is considered an adaptive response to different environments, but to what extent this response is accompanied by genetic differentiation is less clear since it may be phenotypic plasticity. In this study, we analyzed phenotypic variation between two Banksia attenuata growth forms, lignotuberous (shrub) and epicormic resprouting (tree), in fire-prone environments to identify the environmental factors that have driven this phenotypic divergence. We linked genotype with phenotype and traced candidate genes using differential gene expression analysis. Fire intervals determined the phenotypic divergence between growth forms in B. attenuata. A genome-wide association study identified 69 single nucleotide polymorphisms, putatively associated with growth form, whereas no growth form- or phenotype-specific genotypes were identified. Genomic differentiation between the two growth forms was low (F = 0.024). Differential gene expression analysis identified 37 genes/transcripts that were differentially expressed in the two growth forms. A small heat-shock protein gene, associated with lignotuber presence, was differentially expressed in the two forms. We conclude that different fire regimes induce phenotypic polymorphism in B. attenuata, whereas phenotypic trait divergence involves the differential expression of a small fraction of genes that interact strongly with the disturbance regime. Thus, phenotypic plasticity among resprouters is the general strategy for surviving varying fire regimes.