Evidence map›Paper›PMID 33113287›Full record

ArticleMolecular ecology2021

Zooming on dynamics of marine microbial communities in the phycosphere of Akashiwo sanguinea (Dinophyta) blooms.

Junsu Kang, Joon Sang Park, Seung Won Jung, Hyun-Jung Kim, Hyoung Min Joo, Donhyug Kang, Hyojeong Seo, Sunju Kim, Min-Chul Jang, Kyun-Woo Lee and 3 more

Open access · hybridAbstract read
In one paragraph

Article in Molecular ecology, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
2.7field-weighted citation impact, top 10% of its field
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

9 citing papers in PubMed, 32 citations in OpenAlex.

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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

13 authors at 4 institutions in 1 country.

Junsu KangLibrary of Marine Samples, Korea Institute of Ocean Science & Technology, Geoje, Korea.
Joon Sang ParkLibrary of Marine Samples, Korea Institute of Ocean Science & Technology, Geoje, Korea.ORCID 0000-0003-1945-2210
Seung Won JungLibrary of Marine Samples, Korea Institute of Ocean Science & Technology, Geoje, Korea.ORCID 0000-0002-7473-7924
Hyun-Jung KimLibrary of Marine Samples, Korea Institute of Ocean Science & Technology, Geoje, Korea.
Hyoung Min JooDivision of Polar Ocean Science, Korea Polar Research Institute, Incheon, Korea.
Donhyug KangMaritime Security Research Center, Korea Institute of Ocean Science & Technology, Busan, Korea.
Hyojeong SeoDepartment of Oceanography, Pukyong National University, Busan, Korea.
Sunju KimDepartment of Oceanography, Pukyong National University, Busan, Korea.
Min-Chul JangBallast Water Research Center, Korea Institute of Ocean Science & Technology, Geoje, Korea.
Kyun-Woo LeeMarine Biotechnology Research Center, Korea Institute of Ocean Science & Technology, Busan, Korea.
Seok Jin OhDepartment of Oceanography, Pukyong National University, Busan, Korea.
Sukchan LeeDepartment of Genetic Engineering, Sungkyunkwan University, Suwon, Korea.
Taek-Kyun LeeRisk Assessment Research Center, Korea Institute of Ocean Science & Technology, Geoje, Korea.ORCID 0000-0001-6090-507X
Korea Institute of Ocean Science and Technology · KRPukyong National University · KRKorea Polar Research Institute · KRSungkyunkwan University · KR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Characterizing ecological relationships between viruses, bacteria and phytoplankton in the ocean is critical to understanding the ecosystem; however, these relationships are infrequently investigated together. To understand the dynamics of microbial communities and environmental factors in harmful algal blooms (HABs), we examined the environmental factors and microbial communities during Akashiwo sanguinea HABs in the Jangmok coastal waters of South Korea by metagenomics. Specific bacterial species showed complex synergistic and antagonistic relationships with the A. sanguinea bloom. The endoparasitic dinoflagellate Amoebophrya sp. 1 controlled the bloom dynamics and correlated with HAB decline. Among nucleocytoplasmic large DNA viruses (NCLDVs), two Pandoraviruses and six Phycodnaviruses were strongly and positively correlated with the HABs. Operational taxonomic units of microbial communities and environmental factors associated with A. sanguinea were visualized by network analysis: A. sanguinea-Amoebophrya sp. 1 (r = .59, time lag: 2 days) and A. sanguinea-Ectocarpus siliculosus virus 1 in Phycodnaviridae (0.50, 4 days) relationships showed close associations. The relationship between A. sanguinea and dissolved inorganic phosphorus relationship also showed a very close correlation (0.74, 0 day). Microbial communities and the environment changed dynamically during the A. sanguinea bloom, and the rapid turnover of microorganisms responded to ecological interactions. A. sanguinea bloom dramatically changes the environments by exuding dissolved carbohydrates via autotrophic processes, followed by changes in microbial communities involving host-specific viruses, bacteria and parasitoids. Thus, the microbial communities in HAB are composed of various organisms that interact in a complex manner.

Indexed as

DinoflagellidaMicrobiotaHarmful Algal BloomPhytoplanktonRepublic of KoreaAkashiwo sanguineaendoparasitic Amoebophrya sp.environmental changeharmful algal bloommicrobial community nucleocytoplasmic large DNA viruses

Identifiers

PMID33113287
PMCPMC7839783
OpenAlexW3095544956

What OpenQuestion holds

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LicenceCC BY-NC
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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.