Evidence map›Paper›PMID 41686828›Full record

ArticlePloS one2026

Coral larval aquaculture: Species-specific survival and microbial dynamics in flow-through systems.

Blake D Ramsby, Ramona Brunner, Jonathan Barton, Sophie Ferguson, Clare Grimm, Yilmaz Can Hiçyilmaz, David G Bourne, Andrew P Negri, Andrea Severati, Yui Sato and 1 more

Abstract read
In one paragraph

Article in PloS one, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

11 authors.

Blake D RamsbyAustralian Institute of Marine Science, Townsville MC, Townsville, Queensland, Australia.ORCID https://orcid.org/0000-0001-9961-945X
Ramona BrunnerCollege of Science and Engineering, James Cook University, Townsville, Queensland, Australia.
Jonathan BartonAustralian Institute of Marine Science, Townsville MC, Townsville, Queensland, Australia.
Sophie FergusonAustralian Institute of Marine Science, Townsville MC, Townsville, Queensland, Australia.
Clare GrimmAustralian Institute of Marine Science, Townsville MC, Townsville, Queensland, Australia.
Yilmaz Can HiçyilmazAustralian Institute of Marine Science, Townsville MC, Townsville, Queensland, Australia.
David G BourneAustralian Institute of Marine Science, Townsville MC, Townsville, Queensland, Australia.
Andrew P NegriAustralian Institute of Marine Science, Townsville MC, Townsville, Queensland, Australia.
Andrea SeveratiAustralian Institute of Marine Science, Townsville MC, Townsville, Queensland, Australia.
Yui SatoAustralian Institute of Marine Science, Townsville MC, Townsville, Queensland, Australia.
Muhammad Azmi Abdul WahabAustralian Institute of Marine Science, Townsville MC, Townsville, Queensland, Australia.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

To enable burgeoning reef restoration efforts, the production of coral larvae in captive aquaculture needs to maximize survival and yields. While current coral larval rearing methods are generally successful, the approaches vary, and larval yields can be limited due to gradual declines in larval quality or sudden crashes. Here, we reared Acropora sp. nov. aff. kenti and Acropora spathulata larvae for seven days under different stocking densities (0.3, 1.0, or 2.0 larvae mL-1), water volume turnover rates (0.2 or 0.6 vol. hr-1), and with or without UV sterilization and surface agitation, to evaluate their effects on larval survival. Overall, culture treatments had minimal impact on the high larval survival of A. sp. nov. aff. kenti after seven days in culture. However, A. spathulata declined to less than half of the stocking density regardless of culture treatment. Other larval performance metrics including visual appearance and size were not different between the culture treatments. Microbial community composition of the culture water, assessed through 16S rRNA gene sequencing, showed varied community structure between turnover treatments for A. sp. nov. aff. kenti but not for A. spathulata, suggesting species-specific or dynamic responses to water exchange rates. Larval culture water quality parameters (including dissolved and particulate C and N) were consistent across treatments, although reduced water turnover briefly lowered nitrate and nitrite concentrations, coinciding with elevated particulate carbon. This correlated with an increase in potential denitrifying bacteria within the Gammaproteobacteria, suggesting longer residence times of culture water can increase microbial activity. These results demonstrate that large-volume flow-through systems are a robust method for achieving high larval yields for some species and underscore the importance of understanding species-specific survival dynamics to optimize coral aquaculture for large-scale reef restoration.

Indexed as

AnthozoaAquacultureAnimalsCoral ReefsLarvaRNA, Ribosomal, 16SSpecies SpecificityRNA, Ribosomal, 16S

Identifiers

PMID41686828
PMCPMC12904410

What OpenQuestion holds

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.