Evidence map›Paper›PMID 39799374›Full record

ArticleEnvironmental microbiome2025

Low impact of Zostera marina meadows on sediment and water microbiota under brackish conditions.

Daniel P R Herlemann, Luis F Delgado, David J Riedinger, Víctor Fernández-Juárez, Anders F Andersson, Christian Pansch, Lasse Riemann, Mia M Bengtsson, Greta Gyraitė, Marija Kataržytė and 6 more

Abstract read
In one paragraph

Article in Environmental microbiome, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

2 citing papers in PubMed.

  1. Article
  2. Article
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

16 authors.

Daniel P R HerlemannBiological Oceanography, Leibniz Institute for Baltic Sea Research Warnemünde (IOW), 18119, Rostock, Germany. daniel.herlemann@io-warnemuende.de.
Luis F DelgadoScience for Life Laboratory, School of Biotechnology, Division of Gene Technology, KTH Royal Institute of Technology, Solna, 171 21, Sweden.
David J RiedingerBiological Oceanography, Leibniz Institute for Baltic Sea Research Warnemünde (IOW), 18119, Rostock, Germany.
Víctor Fernández-JuárezDepartment of Biology, University of Copenhagen, Helsingør, 3000, Denmark.
Anders F AnderssonScience for Life Laboratory, School of Biotechnology, Division of Gene Technology, KTH Royal Institute of Technology, Solna, 171 21, Sweden.
Christian PanschFaculty of Science and Engineering, Environmental and Marine Biology, Åbo Akademi University, Turku/Åbo, 20500, Finland.
Lasse RiemannDepartment of Biology, University of Copenhagen, Helsingør, 3000, Denmark.
Mia M BengtssonInstitute of Microbiology, University of Greifswald, 17489, Greifswald, Germany.
Greta GyraitėMarine Research Institute, Klaipėda University, Klaipėda, 92294, Lithuania.
Marija KataržytėMarine Research Institute, Klaipėda University, Klaipėda, 92294, Lithuania.
Veljo KisandCenter for Limnology, Estonian University of Life Sciences, Tartu, 51006, Estonia.
Sandra KubeBiological Oceanography, Leibniz Institute for Baltic Sea Research Warnemünde (IOW), 18119, Rostock, Germany.
Georg MartinEstonian Marine Institute, University of Tartu, Tallinn, 12618, Estonia.
Kasia PiwoszNational Marine Fisheries Research Institute, Gdynia, 81-332, Poland.
Marcin RakowskiNational Marine Fisheries Research Institute, Gdynia, 81-332, Poland.
Matthias LabrenzBiological Oceanography, Leibniz Institute for Baltic Sea Research Warnemünde (IOW), 18119, Rostock, Germany.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundZostera marina is an important ecosystem engineer influencing shallow water environments and possibly shaping the microbiota in surrounding sediments and water. Z. marina is typically found in marine systems, but it can also proliferate under brackish conditions. Changes in salinity generally have a strong impact on the biota, especially at the salty divide between salinity 6 and 9. To better understand the impact of the salty divide on the interaction between Z. marina and the surrounding sediment and water microbiota, we investigated the effects of Z. marina meadows on the surrounding microbiota across a salinity range of 6-15 in the Baltic Sea during the summer using 16S and 18S rRNA gene amplicon sequencing.

resultsSalinity was the most important factor for structuring the microbiota within both water and sediment. The presence of Z. marina affected the composition of the bacterial and eukaryotic community and bacterial alpha diversity in the sediment. However, this effect was confined to alpha-mesohaline conditions (salinity 9-15). The impact of Z. marina below salinity 9 on water and sediment microbiota was insignificant.

conclusionsIncreasing salinity was associated with a longer leaf length of Z. marina, causing an increased canopy height, which affects the sediment microbiota through reduced water velocity. Hence, we propose that the canopy effect may be the major predictor explaining Z. marina's interactions with the surrounding microbiota at salinity 9-15. These findings emphasize the importance of the physical effects of Z. marina meadow ecosystem services and have important implications for Z. marina management under brackish conditions in a changing climate.

Indexed as

Bacterial communityBaltic SeaCoastal zoneEelgrassHorohalinicumLittoralMicroeukaryotic communitySalinitySeagrass

Identifiers

PMID39799374
PMCPMC11724437

What Socratic holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

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 Socratic graph.