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Reef-building crustose coralline algae (CCA) are known to facilitate the settlement and metamorphosis of scleractinian coral larvae. In recent decades, CCA coverage has fallen globally and degrading environmental conditions continue to reduce coral survivorship, spurring new restoration interventions to rebuild coral reef health. In this study, naturally produced chemical compounds (metabolites) were collected from two pantropical CCA genera to isolate and classify those that induce coral settlement. In experiments using four ecologically important Caribbean coral species, we demonstrate the applicability of extracted, CCA-derived metabolites to improve larval settlement success in coral breeding and restoration efforts. Tissue-associated CCA metabolites induced settlement of one coral species,Orbicella faveolata, while metabolites exuded by CCA (exometabolites) induced settlement of three species:Acropora palmata,Colpophyllia natansandOrbicella faveolata. In a follow-up experiment, CCA exometabolites fractionated and preserved using two different extraction resins induced the same level of larval settlement as the unfractionated positive control exometabolites. The fractionated CCA exometabolite pools were characterized using liquid chromatography tandem mass spectrometry, yielding 145 distinct molecular subnetworks that were statistically defined as CCA-derived and could be classified into 10 broad chemical classes. Identifying these compounds can reveal their natural prevalence in coral reef habitats and facilitate the development of new applications to enhance larval settlement and the survival of coral juveniles. 

Reversing coral reef decline requires reducing environmental threats while actively restoring reef ecological structure and function. A promising restoration approach uses coral breeding to boost natural recruitment and repopulate reefs with genetically diverse coral communities. Recent advances in predicting spawning, capturing spawn, culturing larvae, and rearing settlers have enabled the successful propagation, settlement, and outplanting of coral offspring in all of the world's major reef regions. Nevertheless, breeding efforts frequently yield low survival, reflecting the type III survivorship curve of corals and poor condition of most reefs targeted for restoration. Furthermore, coral breeding programs are still limited in spatial scale and species diversity. Here, we highlight four priority areas for research and cooperative innovation to increase the effectiveness and scale of coral breeding in restoration: (1) expanding the number of restoration sites and species, (2) improving broodstock selection to maximize the genetic diversity and adaptive capacity of restored populations, (3) enhancing culture conditions to improve offspring health before and after outplanting, and (4) scaling up infrastructure and technologies for large‐scale coral breeding and restoration. Prioritizing efforts in these four areas will enable practitioners to address reef decline at relevant ecological scales, re‐establish self‐sustaining coral populations, and ensure the long‐term success of restoration interventions. Overall, we aim to guide the coral restoration community toward actions and opportunities that can yield rapid technical advances in larval rearing and coral breeding, foster interdisciplinary collaborations, and ultimately achieve the ecological restoration of coral reefs. 

Since 1892, it has been widely assumed that somatic mutations are evolutionarily irrelevant in animals because they cannot be inherited by offspring. However, some nonbilaterians segregate the soma and germline late in development or never, leaving the evolutionary fate of their somatic mutations unknown. By investigating uni- and biparental reproduction in the coralAcropora palmata(Cnidaria, Anthozoa), we found that uniparental, meiotic offspring harbored 50% of the 268 somatic mutations present in their parent. Thus, somatic mutations accumulated in adult coral animals, entered the germline, and were passed on to swimming larvae that grew into healthy juvenile corals. In this way, somatic mutations can increase allelic diversity and facilitate adaptation across habitats and generations in animals.