Evidence map›Paper›PMID 39531470›Full record

ArticlePLoS biology2024

Coral larvae increase nitrogen assimilation to stabilize algal symbiosis and combat bleaching under increased temperature.

Ariana S Huffmyer, Jill Ashey, Emma Strand, Eric N Chiles, Xiaoyang Su, Hollie M Putnam

Abstract read
In one paragraph

Article in PLoS biology, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing 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

5 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
  4. Hypoxia disrupts metabolism in coral and sea anemone larvae.The Journal of experimental biology · 2025
    Article
  5. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

6 authors.

Ariana S HuffmyerSchool of Aquatic and Fisheries Sciences, University of Washington, Seattle, Washington United States of America.ORCID 0000-0002-9170-0971
Jill AsheyDepartment of Biological Sciences, University of Rhode Island, Kingston, Rhode Island United States of America.ORCID 0000-0001-5499-9786
Emma StrandDepartment of Biological Sciences, University of Rhode Island, Kingston, Rhode Island United States of America.ORCID 0000-0003-4227-8345
Eric N ChilesMicrobial Biology Graduate Program, Rutgers University, New Brunswick, New Jersey United States of America.ORCID 0000-0003-3354-607X
Xiaoyang SuMetabolomics Shared Resource, Rutgers Cancer Institute of New Jersey, Rutgers University, New Brunswick, New Jersey United States of America.ORCID 0000-0001-8081-1396
Hollie M PutnamDepartment of Biological Sciences, University of Rhode Island, Kingston, Rhode Island United States of America.ORCID 0000-0003-2322-3269

Funding

National Science Foundation 2205966National Science Foundation EF-1921465
6 · The paper itself

Abstract

Rising sea surface temperatures are increasingly causing breakdown in the nutritional relationship between corals and algal endosymbionts (Symbiodiniaceae), threatening the basis of coral reef ecosystems and highlighting the critical role of coral reproduction in reef maintenance. The effects of thermal stress on metabolic exchange (i.e., transfer of fixed carbon photosynthates from symbiont to host) during sensitive early life stages, however, remains understudied. We exposed symbiotic Montipora capitata coral larvae in Hawai'i to high temperature (+2.5°C for 3 days), assessed rates of photosynthesis and respiration, and used stable isotope tracing (4 mM 13C sodium bicarbonate; 4.5 h) to quantify metabolite exchange. While larvae did not show any signs of bleaching and did not experience declines in survival and settlement, metabolic depression was significant under high temperature, indicated by a 19% reduction in respiration rates, but with no change in photosynthesis. Larvae exposed to high temperature showed evidence for maintained translocation of a major photosynthate, glucose, from the symbiont, but there was reduced metabolism of glucose through central carbon metabolism (i.e., glycolysis). The larval host invested in nitrogen cycling by increasing ammonium assimilation, urea metabolism, and sequestration of nitrogen into dipeptides, a mechanism that may support the maintenance of glucose translocation under thermal stress. Host nitrogen assimilation via dipeptide synthesis appears to be used for nitrogen limitation to the Symbiodiniaceae, and we hypothesize that nitrogen limitation contributes to retention of fixed carbon by favoring photosynthate translocation to the host. Collectively, our findings indicate that although these larvae are susceptible to metabolic stress under high temperature, diverting energy to nitrogen assimilation to maintain symbiont population density, photosynthesis, and carbon translocation may allow larvae to avoid bleaching and highlights potential life stage specific metabolic responses to stress.

Indexed as

AnthozoaLarvaNitrogenPhotosynthesisSymbiosisAnimalsCarbonCoral ReefsDinoflagellidaHawaiiHot TemperatureTemperatureCarbonNitrogen

Identifiers

PMID39531470
PMCPMC11556732

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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.