Spatial variability of prokaryotic and viral abundances in the Kermadec and Atacama Trench regions-Reference-Cited by-同舟云学术

Spatial variability of prokaryotic and viral abundances in the Kermadec and Atacama Trench regions

Published:2021-02-28 Issue:6 Volume:66 Page:2095-2109
ISSN:0024-3590
Container-title:Limnology and Oceanography
language:en
Short-container-title:Limnol Oceanogr

Author:

Schauberger Clemens¹^ORCID,Middelboe Mathias¹²^ORCID,Larsen Morten¹^ORCID,Peoples Logan M.³^ORCID,Bartlett Douglas H.³^ORCID,Kirpekar Finn⁴^ORCID,Rowden Ashley A.⁵⁶^ORCID,Wenzhöfer Frank⁷⁸^ORCID,Thamdrup Bo¹^ORCID,Glud Ronnie N.¹⁹¹⁰^ORCID

Affiliation:

1. Department of Biology, Nordcee and HADAL University of Southern Denmark Odense Denmark

2. Marine Biological Section, Department of Biology University of Copenhagen Helsingør Denmark

3. Marine Biology Research Division, Scripps Institution of Oceanography University of California San Diego La Jolla California USA

4. Department of Biochemistry and Molecular Biology University of Southern Denmark Odense M Denmark

5. National Institute of Water and Atmospheric Research Wellington New Zealand

6. School of Biological Sciences, Victoria University of Wellington Wellington New Zealand

7. Alfred Wegener Institute, Helmholtz Center for Polar and Marine Research Bremerhaven Germany

8. Max Planck Institute for Marine Microbiology and Ecology Bremen Germany

9. Department of Ocean and Environmental Sciences Tokyo University of Marine Science and Technology Tokyo Japan

10. Danish Institute for Advanced Study – DIAS, University of Southern Denmark Odense Denmark

Funder

Bundesministerium für Bildung und Forschung

Danmarks Grundforskningsfond

H2020 European Research Council

National Institute of Water and Atmospheric Research

Publisher

Wiley

Subject

Aquatic Science,Oceanography

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/lno.11711

Reference62 articles.

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4. Vertical zonation patterns of scavenging amphipods from the Hadal zone of the Tonga and Kermadec Trenches

5. Optimization of Procedures for Counting Viruses by Flow Cytometry

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