Reference health
Viruses manipulate the marine environment
69/69 checkable references clean · checked 2026-08-28
Every reference with a DOI in the deposited reference list resolved to a known work in Crossref or DataCite at the dated check, and none carried a retraction, withdrawal, or removal notice.
4 without a DOI — not checked. A reference deposited without a DOI is never matched by title or guessed at; it stays outside the checked set, and this line discloses that.
The 69 checked references that resolve
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Global-scale processes with a nanoscale drive: the role of marine viruses
resolves10.4319/lo.2000.45.8.1697
Genome size distributions indicate variability and similarities among marine viral assemblages from diverse environments
resolves10.1128/AEM.65.1.231-240.1999
Population Dynamics of Chesapeake Bay Virioplankton: Total-Community Analysis by Pulsed-Field Gel Electrophoresis
resolves10.1098/rspb.2003.2628
Diversity and population structure of a near–shore marine–sediment viral community
resolves10.1038/nature06735
Biodiversity and biogeography of phages in modern stromatolites and thrombolites
resolves10.1186/1471-2164-8-456
Horizontal gene transfer and nucleotide compositional anomaly in large DNA viruses
resolves10.1038/ismej.2008.35
Prophages in marine bacteria: dangerous molecular time bombs or the key to survival in the seas?
resolves10.1128/MMBR.63.1.106-127.1999
<i>Prochlorococcus</i>
, a Marine Photosynthetic Prokaryote of Global Significance
resolves10.1128/JB.187.9.3188-3200.2005
The Genome of S-PM2, a “Photosynthetic” T4-Type Bacteriophage That Infects Marine
<i>Synechococcus</i>
Strains
resolves10.1371/journal.pbio.0040234
Prevalence and Evolution of Core Photosystem II Genes in Marine Cyanobacterial Viruses and Their Hosts
resolves10.1038/nature04111
Photosynthesis genes in marine viruses yield proteins during host infection
resolves10.1371/journal.pbio.0030144
Three Prochlorococcus Cyanophage Genomes: Signature Features and Ecological Interpretations
resolves10.1126/science.1122050
Genomic Islands and the Ecology and Evolution of
<i>Prochlorococcus</i>
resolves10.1038/ismej.2007.67
Viral photosynthetic reaction center genes and transcripts in the marine environment
resolves10.1126/science.272.5270.1910
Lysogenic Conversion by a Filamentous Phage Encoding Cholera Toxin
resolves10.1038/ismej.2008.73
Lysogenic virus–host interactions predominate at deep-sea diffuse-flow hydrothermal vents
resolves10.1016/j.anaerobe.2007.03.004
Prophage-like gene transfer agents—Novel mechanisms of gene exchange for Methanococcus, Desulfovibrio, Brachyspira, and Rhodobacter species
resolves10.1016/j.tim.2006.12.001
Importance of widespread gene transfer agent genes in α-proteobacteria
resolves10.1128/AEM.02129-07
Occurrence and Expression of Gene Transfer Agent Genes in Marine Bacterioplankton
resolves10.1264/jsme2.2002.53
Broad Host Range Xenotrophic Gene Transfer by Virus-Like Particles from a Hot Spring.
resolves10.1111/j.1574-6968.2004.tb09654.x
Global distribution of nearly identical phage-encoded DNA sequences
resolves10.1128/AEM.71.1.480-486.2005
Nearly Identical Bacteriophage Structural Gene Sequences Are Widely Distributed in both Marine and Freshwater Environments
resolves10.1111/j.1574-695X.2007.00232.x
Pathogenic and opportunistic free-living amoebae:
<i>Acanthamoeba</i>
spp.,
<i>Balamuthia mandrillaris</i>
,
<i>Naegleria fowleri</i>
, and
<i>Sappinia diploidea</i>
resolves10.1016/j.tig.2006.11.002
I am what I eat and I eat what I am: acquisition of bacterial genes by giant viruses
resolves10.2216/i0031-8884-40-6-503.1
A review of the coccolithophorid Emiliania huxleyi (Prymnesiophyceae), with particular reference to growth, coccolith formation, and calcification-photosynthesis interactions
resolves10.3354/meps093039
Viral mortality of the marine alga Emiliania huxleyi (Haptophyceae) and termination of algal blooms
resolves10.1016/S0967-0645(02)00065-6
Virus dynamics in a coccolithophore-dominated bloom in the North Sea
resolves10.1017/S002531540200560X
Isolation of viruses responsible for the demise of an <i>Emiliania huxleyi</i> bloom in the English Channel
resolves10.1126/science.1113109
Complete Genome Sequence and Lytic Phase Transcription Profile of a
<i>Coccolithovirus</i>
resolves10.1073/pnas.0701240104
Viral activation and recruitment of metacaspases in the unicellular coccolithophore,
<i>Emiliania huxleyi</i>
resolves10.1006/viro.2001.1238
Caspase Activation Is Required for Permissive Replication of Aleutian Mink Disease Parvovirus in Vitro
resolves10.1016/j.virol.2003.11.025
Caspase activation during virus infection: more than just the kiss of death?
resolves10.1073/pnas.0807707105
The “Cheshire Cat” escape strategy of the coccolithophore
<i>Emiliania huxleyi</i>
in response to viral infection
resolves10.1073/pnas.93.22.12333
Chloroplast genes are expressed during intracellular symbiotic association of Vaucheria litorea plastids with the sea slug Elysia chlorotica.
resolves10.1104/pp.124.1.331
Mollusc-Algal Chloroplast Endosymbiosis. Photosynthesis, Thylakoid Protein Maintenance, and Chloroplast Gene Expression Continue for Many Months in the Absence of the Algal Nucleus
resolves10.2307/1543594
Horizontal Transfer of Functional Nuclear Genes Between Multicellular Organisms
resolves10.2307/1542990
Annual Viral Expression in a Sea Slug Population: Life Cycle Control and Symbiotic Chloroplast Maintenance
resolves10.1111/j.1744-7410.2003.tb00078.x
Apoptotic‐like morphology is associated with annual synchronized death in kleptoplastic sea slugs (<i>Elysia chlorotica</i>)
resolves10.1371/journal.ppat.0020043
The Tripartite Associations between Bacteriophage, Wolbachia, and Arthropods
resolves10.1073/pnas.0507029102
The players in a mutualistic symbiosis: Insects, bacteria, viruses, and virulence genes
resolves10.1006/viro.1999.9837
The Complete Genome Sequence of PM2, the First Lipid-Containing Bacterial Virus To Be Isolated
resolves10.1128/AEM.37.4.774-778.1979
Evidence by electron micrographs for a high incidence of bacteriophage particles in the waters of Yaquina Bay, oregon: ecological and taxonomical implications
resolves10.4319/lo.1995.40.7.1236
Viruses and protists cause similar bacterial mortality in coastal seawater
resolves10.4319/lo.1997.42.7.1492
Release and bioavailability of C, N, P Se, and Fe following viral lysis of a marine chrysophyte
resolves10.4319/lo.2000.45.2.0408
The complete genomic sequence of the marine phage Roseophage SIO1 shares homology with nonmarine phages
resolves10.1186/1743-422X-4-69
The complete genomes of three viruses assembled from shotgun libraries of marine RNA virus communities
resolves10.1111/j.1462-2920.2006.01006.x
Genetic richness of vibriophages isolated in a coastal environment
resolves10.1007/s002489900079
Significance of Lysogeny in the Marine Environment: Studies with Isolates and a Model of Lysogenic Phage Production
resolves10.1128/AEM.71.6.3311-3320.2005
Complete Genome Sequence of φHSIC, a Pseudotemperate Marine Phage of
<i>Listonella pelagia</i>
The 4 references without a DOI — listed, not checked
no DOI — not checkedKlaveness, D. & Paasche, E. Two different Coccolithus huxleyi cell types incapable of coccolith formation. Arch. Microbiol. 75, 382–385 (1971).
no DOI — not checkedPierce, S. K., Curtis, N. E., Hanten, J. J., Boerner, S. L. & Schwartz, J. A. Transfer, integration and expression of functional nuclear genes between multicellular species. Symbiosis 43, 57–64 (2007).
no DOI — not checkedPierce, S. K., Curtis, N. E., Schwartz, J. A. & Massey, S. E. Functional algal nuclear genes are present in a sea slug genome — horizontal gene transfer demonstrated. Integr. Comp. Biol. 46, e110 (2006).
no DOI — not checkedZobell, C. E. Marine Microbiology (Chronica Botanica, 1946).
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