The DOI matches its Crossref record; 72 of the 72 references it cites were found in a registry or an index.
Genomic Expansion of Domain Archaea Highlights Roles for Organisms from New Phyla in Anaerobic Carbon Cycling
Open accessAbstract
Background Archaea represent a significant fraction of Earth's biodiversity, yet they remain much less well understood than Bacteria. Gene surveys, a few metagenomic studies, and some single-cell sequencing projects have revealed numerous little-studied archaeal phyla. Certain lineages appear to branch deeply and may be part of a major phylum radiation. The structure of this radiation and the physiology of the organisms remain almost unknown. Results We used genome-resolved metagenomic analyses to investigate the diversity, genomes sizes, metabolic capacities, and potential roles of Archaea in terrestrial subsurface biogeochemical cycles. We sequenced DNA from complex sediment and planktonic consortia from an aquifer adjacent to the Colorado River (USA) and reconstructed the first complete genomes for Archaea using cultivation-independent methods. To provide taxonomic context, we analyzed an additional 151 newly sampled archaeal sequences. We resolved two new phyla within a major, apparently deep-branching group of phyla (a superphylum). The organisms have small genomes, and metabolic predictions indicate that their primary contributions to Earth's biogeochemical cycles involve carbon and hydrogen metabolism, probably associated with symbiotic and/or fermentation-based lifestyles. Conclusions The results dramatically expand genomic sampling of the domain Archaea and clarify taxonomic designations within a major superphylum. This study, in combination with recently published work on bacterial phyla lacking cultivated representatives, reveals a fascinating phenomenon of major radiations of organisms with small genomes, novel proteome composition, and strong interdependence in both domains.
Overview
Integrity signals
Registry
Cites
Statistics
Verification
Claims the paper makes
Claims other papers make about this one
Each is checked against this paper’s own text: does it say what the citing paper says it does?
In the citing paper
“Trees visualized at https://itol.embl.de/itol.cgiusing Netwick files from Hug et al. (2016) concatenated ribosomal proteins in place of 16S rRNA genes (Fig. 3B) indicate that a large radiation of predominantly uncultured mesophilic taxa, which are comprised of potentially symbiotic organisms with small cells and genomes and are referred to as the bacterial candidate phyla radiation (CPR) and the”
From The Emergence of Life (2019) · cites this paper as Castelle et al. 2015
Citations
Cites
Basic local alignment search tool
Altschul, S. F., Gish, W., Miller, W., Myers, E. W., & Lipman, D. J. (1990) · Journal of Molecular Biology · doi:10.1006/jmbi.1990.9999 · Cited by 98,669
Fast gapped-read alignment with Bowtie 2
Langmead, B., & Salzberg, S. L. (2012) · Nature Methods · doi:10.1038/nmeth.1923 · Cited by 56,400
MUSCLE: multiple sequence alignment with high accuracy and high throughput
Edgar, R. C. (2004) · Nucleic Acids Research · doi:10.1093/nar/gkh340 · Cited by 44,662
A Simple, Fast, and Accurate Algorithm to Estimate Large Phylogenies by Maximum Likelihood
Guindon, S., & Gascuel, O. (2003) · Systematic Biology · doi:10.1080/10635150390235520 · Cited by 16,923
RAxML-VI-HPC: maximum likelihood-based phylogenetic analyses with thousands of taxa and mixed models
Stamatakis, A. (2006) · Bioinformatics · doi:10.1093/bioinformatics/btl446 · Cited by 15,582
tRNAscan-SE: A Program for Improved Detection of Transfer RNA Genes in Genomic Sequence
Lowe, T. M., & Eddy, S. R. (1997) · Nucleic Acids Research · doi:10.1093/nar/25.5.955 · Cited by 11,200
MUSCLE: a multiple sequence alignment method with reduced time and space complexity
Edgar, R. C. (2004) · BMC Bioinformatics · doi:10.1186/1471-2105-5-113 · Cited by 9,119
Pruesse, E., Quast, C., Knittel, K., Fuchs, B. M., Ludwig, W., Peplies, J., & Glöckner, F. O. (2007) · Nucleic Acids Research · doi:10.1093/nar/gkm864 · Cited by 6,682
Pfam: the protein families database
Finn, R. D., Bateman, A., Clements, J., Coggill, P., Eberhardt, R. Y., Eddy, S. R., Heger, A., Hetherington, K., Holm, L., Mistry, J., et al. (2014) · Nucleic Acids Research · doi:10.1093/nar/gkt1223 · Cited by 6,148
Towards a natural system of organisms: proposal for the domains Archaea, Bacteria, and Eucarya.
Woese, C. R., Kandler, O., & Wheelis, M. L. (1990) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.87.12.4576 · Cited by 6,128
Peng, Y., Leung, H. C. M., Yiu, S., & Chin, F. Y. L. (2012) · Bioinformatics · doi:10.1093/bioinformatics/bts174 · Cited by 2,998
Isolation of an autotrophic ammonia-oxidizing marine archaeon
Könneke, M., Bernhard, A. E., de la Torre, J. R., Walker, C. B., Waterbury, J. B., & Stahl, D. A. (2005) · Nature · doi:10.1038/nature03911 · Cited by 2,864
Archaea in coastal marine environments.
DeLong, E. F. (1992) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.89.12.5685 · Cited by 2,758
Community structure and metabolism through reconstruction of microbial genomes from the environment
Tyson, G. W., Chapman, J., Hugenholtz, P., Allen, E. E., Ram, R. J., Richardson, P. M., Solovyev, V. V., Rubin, E. M., Rokhsar, D. S., & Banfield, J. F. (2004) · Nature · doi:10.1038/nature02340 · Cited by 2,417
Self-citationInsights into the phylogeny and coding potential of microbial dark matter
Rinke, C., Schwientek, P., Sczyrba, A., Ivanova, N. N., Anderson, I. J., Cheng, J.-F., Darling, A., Malfatti, S., Swan, B. K., Gies, E. A., et al. (2013) · Nature · doi:10.1038/nature12352 · Cited by 2,394
UniRef: comprehensive and non-redundant UniProt reference clusters
Suzek, B. E., Huang, H., McGarvey, P., Mazumder, R., & Wu, C. H. (2007) · Bioinformatics · doi:10.1093/bioinformatics/btm098 · Cited by 1,613
Mesophilic crenarchaeota: proposal for a third archaeal phylum, the Thaumarchaeota
Brochier‐Armanet, C., Boussau, B., Gribaldo, S., & Forterre, P. (2008) · Nature Reviews Microbiology · doi:10.1038/nrmicro1852 · Cited by 1,249
Novel Division Level Bacterial Diversity in a Yellowstone Hot Spring
Hugenholtz, P., Pitulle, C., Hershberger, K. L., & Pace, N. R. (1998) · Journal of Bacteriology · doi:10.1128/jb.180.2.366-376.1998 · Cited by 891
A new phylum of Archaea represented by a nanosized hyperthermophilic symbiont
Huber, H., Hohn, M. J., Rachel, R., Fuchs, T., Wimmer, V. C., & STETTER, K. O. (2002) · Nature · doi:10.1038/417063a · Cited by 825
Autotrophic carbon fixation in archaea
Berg, I. A., Kockelkorn, D., Ramos-Vera, W. H., Say, R. F., Zarzycki, J., Hügler, M., Alber, B. E., & Fuchs, G. (2010) · Nature Reviews Microbiology · doi:10.1038/nrmicro2365 · Cited by 719
Structures and mechanisms of glycosyltransferases
Breton, C., Šnajdrová, L., Jeanneau, C., Koča, J., & Imberty, A. (2005) · Glycobiology · doi:10.1093/glycob/cwj016 · Cited by 711
Perspectives on archaeal diversity, thermophily and monophyly from environmental rRNA sequences.
Barns, S. M., Delwiche, C. F., Palmer, J. D., & Pace, N. R. (1996) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.93.17.9188 · Cited by 661
Gene and translation initiation site prediction in metagenomic sequences
Hyatt, D., LoCascio, P. F., Hauser, L., & Uberbacher, E. C. (2012) · Bioinformatics · doi:10.1093/bioinformatics/bts429 · Cited by 655
Fermentation, Hydrogen, and Sulfur Metabolism in Multiple Uncultivated Bacterial Phyla
Wrighton, K. C., Thomas, B. C., Sharon, I., Miller, C. S., Castelle, C. J., VerBerkmoes, N. C., Wilkins, M. J., Hettich, R. L., Lipton, M. S. W., Williams, K. H., et al. (2012) · Science · doi:10.1126/science.1224041 · Cited by 654
Self-citationHug, L. A., Castelle, C. J., Wrighton, K. C., Thomas, B. C., Sharon, I., Frischkorn, K. R., Williams, K. H., Tringe, S. G., & Banfield, J. F. (2013) · Microbiome · doi:10.1186/2049-2618-1-22 · Cited by 643
Self-citationDridi, B., Fardeau, M.-L., Ollivier, B., Raoult, D., & Drancourt, M. (2012) · International Journal of Systematic and Evolutionary Microbiology · doi:10.1099/ijs.0.033712-0 · Cited by 596
Predominant archaea in marine sediments degrade detrital proteins
Lloyd, K. G., Schreiber, L., Petersen, D. G., Kjeldsen, K. U., Lever, M. A., Steen, A. D., Stepanauskas, R., Richter, M., Kleindienst, S., Lenk, S., et al. (2013) · Nature · doi:10.1038/nature12033 · Cited by 563
Community-wide analysis of microbial genome sequence signatures
Dick, G. J., Andersson, A. F., Baker, B. J., Simmons, S. L., Thomas, B. C., Yelton, A. P., & Banfield, J. F. (2009) · Genome biology · doi:10.1186/gb-2009-10-8-r85 · Cited by 527
Self-citationThe genome of Nanoarchaeum equitans: Insights into early archaeal evolution and derived parasitism
Waters, E. R., Hohn, M. J., Ahel, I., Graham, D. E., Adams, M. D., Barnstead, M., Beeson, K. Y., Bibbs, L., Bolanos, R. A., Keller, M., et al. (2003) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1735403100 · Cited by 522
Genetic Diversity of Archaea in Deep-Sea Hydrothermal Vent Environments
Takai, K., & Horikoshi, K. (1999) · Genetics · doi:10.1093/genetics/152.4.1285 · Cited by 487
Untangling Genomes from Metagenomes: Revealing an Uncultured Class of Marine Euryarchaeota
Iverson, V., Morris, R. M., Frazar, C. D., Berthiaume, C. T., Morales, R. L., & Armbrust, E. V. (2012) · Science · doi:10.1126/science.1212665 · Cited by 475
Vetriani, C., Jannasch, H. W., MacGregor, B. J., Stahl, D. A., & Reysenbach, A. (1999) · Applied and Environmental Microbiology · doi:10.1128/aem.65.10.4375-4384.1999 · Cited by 458
Atkinson, G. C., Tenson, T., & Hauryliuk, V. (2011) · PLoS ONE · doi:10.1371/journal.pone.0023479 · Cited by 447
ppGpp: magic beyond RNA polymerase
Dalebroux, Z. D., & Swanson, M. S. (2012) · Nature Reviews Microbiology · doi:10.1038/nrmicro2720 · Cited by 434
Genome-Wide Experimental Determination of Barriers to Horizontal Gene Transfer
Sorek, R., Zhu, Y., Creevey, C. J., Francino, M. P., Bork, P., & Rubin, E. M. (2007) · Science · doi:10.1126/science.1147112 · Cited by 421
The archaeal ‘TACK’ superphylum and the origin of eukaryotes
Guy, L., & Ettema, T. J. G. (2011) · Trends in Microbiology · doi:10.1016/j.tim.2011.09.002 · Cited by 372
Narasingarao, P., Podell, S. B., Ugalde, J. A., Brochier‐Armanet, C., Emerson, J., Brocks, J. J., Heidelberg, K. B., Banfield, J. F., & Allen, E. E. (2011) · The ISME Journal · doi:10.1038/ismej.2011.78 · Cited by 364
Self-citationEnigmatic, ultrasmall, uncultivated Archaea
Baker, B. J., Comolli, L. R., Dick, G. J., Hauser, L., Hyatt, D., Dill, B. D., Land, M., VerBerkmoes, N. C., Hettich, R. L., & Banfield, J. F. (2010) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0914470107 · Cited by 337
Self-citationNunoura, T., Takaki, Y., Kakuta, J., Nishi, S., Sugahara, J., Kazama, H., Chee, G.-J., Hattori, M., Kanai, A., Atomi, H., et al. (2010) · Nucleic Acids Research · doi:10.1093/nar/gkq1228 · Cited by 310
Borrel, G., Parisot, N., Harris, H. M. B., Peyretaillade, É., Gaci, N., Tottey, W., Bardot, O., Raymann, K., Gribaldo, S., Peyret, P., et al. (2014) · BMC Genomics · doi:10.1186/1471-2164-15-679 · Cited by 302
Small Genomes and Sparse Metabolisms of Sediment-Associated Bacteria from Four Candidate Phyla
Kantor, R. S., Wrighton, K. C., Handley, K. M., Sharon, I., Hug, L. A., Castelle, C. J., Thomas, B. C., & Banfield, J. F. (2013) · mBio · doi:10.1128/mbio.00708-13 · Cited by 297
Self-citationA korarchaeal genome reveals insights into the evolution of the Archaea
Elkins, J. G., Podar, M., Graham, D. E., Makarova, K. S., Wolf, Y., Randau, L., Hedlund, B. P., Brochier-Armanet, C., Kunin, V., Anderson, I., et al. (2008) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0801980105 · Cited by 296
Meng, J., Xu, J., Qin, D., He, Y., Xiao, X., & Wang, F. (2013) · The ISME Journal · doi:10.1038/ismej.2013.174 · Cited by 284
Search for a 'Tree of Life' in the thicket of the phylogenetic forest
Puigbò, P., Wolf, Y. I., & Koonin, E. V. (2009) · Journal of Biology · doi:10.1186/jbiol159 · Cited by 279
The unique features of glycolytic pathways in Archaea
Verhees, C. H., Kengen, S. W. M., Tuininga, J. E., Schut, G. J., Adams, M. W. W., de Vos, W. M., & John van der, O. O. S. T. (2003) · Biochemical Journal · doi:10.1042/bj20021472 · Cited by 259
Williams, K. H., Long, P. E., Davis, J. A., Wilkins, M. J., N’Guessan, A. L., Steefel, C. I., Yang, L., Newcomer, D. R., Spane, F. A., Kerkhof, L. J., et al. (2011) · Geomicrobiology Journal · doi:10.1080/01490451.2010.520074 · Cited by 257
Self-citationArchaeal Type III RuBisCOs Function in a Pathway for AMP Metabolism
Sato, T., Atomi, H., & Imanaka, T. (2007) · Science · doi:10.1126/science.1135999 · Cited by 237
Giraud, M., & Naismith, J. H. (2000) · Current Opinion in Structural Biology · doi:10.1016/s0959-440x(00)00145-7 · Cited by 235
Lineages of Acidophilic Archaea Revealed by Community Genomic Analysis
Baker, B. J., Tyson, G. W., Webb, R. I., Flanagan, J., Hugenholtz, P., Allen, E. E., & Banfield, J. F. (2006) · Science · doi:10.1126/science.1132690 · Cited by 235
Self-citationExtraordinary phylogenetic diversity and metabolic versatility in aquifer sediment
Castelle, C., Hug, L., Wrighton, K., Thomas, B., Williams, K., Wu, D., Tringe, S., Singer, S., Eisen, J., & Banfield, J. (2013) · Nature Communications · doi:10.1038/ncomms3120 · Cited by 224
Self-citationWrighton, K. C., Castelle, C. J., Wilkins, M. J., Hug, L. A., Sharon, I., Thomas, B. C., Handley, K. M., Mullin, S. W., Nicora, C., Singh, A., et al. (2014) · The ISME Journal · doi:10.1038/ismej.2013.249 · Cited by 185
Self-citationTabita, F. R., Hanson, T. E., Satagopan, S., Witte, B., & Kreel, N. E. (2008) · Philosophical Transactions of the Royal Society B Biological Sciences · doi:10.1098/rstb.2008.0023 · Cited by 158
Enzymes of hydrogen metabolism in Pyrococcus furiosus
Silva, P. J., van den Ban, E. C. D., Wassink, H., Haaker, H., de Castro, B., Robb, F. T., & Hagen, W. R. (2000) · European Journal of Biochemistry · doi:10.1046/j.1432-1327.2000.01745.x · Cited by 141
Bacteriocins : ecology and evolution
Riley, M. A., & Chavan, M. A. (2007) · doi:10.1007/978-3-540-36604-1 · Cited by 137
Podar, M., Makarova, K. S., Graham, D. E., Wolf, Y. I., Koonin, E. V., & Reysenbach, A. (2013) · Biology Direct · doi:10.1186/1745-6150-8-9 · Cited by 111
Youssef, N. H., Rinke, C., Stepanauskas, R., Farag, I., Woyke, T., & Elshahed, M. S. (2014) · The ISME Journal · doi:10.1038/ismej.2014.141 · Cited by 97
Yelton, A. P., Comolli, L. R., Justice, N. B., Castelle, C. J., Denef, V. J., Thomas, B. C., & Banfield, J. F. (2013) · BMC Genomics · doi:10.1186/1471-2164-14-485 · Cited by 92
Self-citationGlasemacher, J., Bock, A., Schmid, R., & Schönheit, P. (1997) · European Journal of Biochemistry · doi:10.1111/j.1432-1033.1997.00561.x · Cited by 87
Hydrogenases and H+-Reduction in Primary Energy Conservation
Vignais, P. M. (2007) · Springer eBooks · doi:10.1007/400_2006_027 · Cited by 69
Inter-species interconnections in acid mine drainage microbial communities
Comolli, L. R., & Banfield, J. F. (2014) · Frontiers in Microbiology · doi:10.3389/fmicb.2014.00367 · Cited by 65
Self-citationOmic Approaches in Microbial Ecology: Charting the Unknown
Baker, B. J., & Dick, G. J. (2013) · Microbe Magazine · doi:10.1128/microbe.8.353.1 · Cited by 65
Aono, R., Sato, T., Yano, A., Yoshida, S., Nishitani, Y., Miki, K., Imanaka, T., & Atomi, H. (2012) · Journal of Bacteriology · doi:10.1128/jb.01335-12 · Cited by 60
Schöcke, L., & Schink, B. (1998) · European Journal of Biochemistry · doi:10.1046/j.1432-1327.1998.2560589.x · Cited by 55
An Automated Phylogenetic Tree-Based Small Subunit rRNA Taxonomy and Alignment Pipeline (STAP)
Wu, D., Hartman, A., Ward, N. L., & Eisen, J. A. (2008) · PLoS ONE · doi:10.1371/journal.pone.0002566 · Cited by 51
The proportional lack of archaeal pathogens: Do viruses/phages hold the key?
Gill, E. E., & Brinkman, F. S. L. (2011) · BioEssays · doi:10.1002/bies.201000091 · Cited by 50
Peptide and Protein Antibiotics from the Domain Archaea: Halocins and Sulfolobicins
Shand, R. F., & Leyva, K. J. (2006) · Springer eBooks · doi:10.1007/978-3-540-36604-1_5 · Cited by 49
Sprott, G. D., Shaw, K. M., & Jarrell, K. F. (1983) · Journal of Biological Chemistry · doi:10.1016/s0021-9258(18)32771-6 · Cited by 45
AMP‐forming acetyl‐CoA synthetases in Archaea show unexpected diversity in substrate utilization
Ingram-Smith, C. J., & Smith, K. S. (2006) · Archaea · doi:10.1155/2006/738517 · Cited by 42
Artola-Recolons, C., Carrasco‐López, C., Llarrull, L. I., Kumarasiri, M., Lastochkin, E., de Ilarduya, I. M., Meindl, K., Usón, I., Mobashery, S., & Hermoso, J. A. (2011) · Biochemistry · doi:10.1021/bi200085y · Cited by 41
Holmes, D. E., Giloteaux, L., Orellana, R., Williams, K. H., Robbins, M. J., & Lovley, D. R. (2014) · Frontiers in Microbiology · doi:10.3389/fmicb.2014.00366 · Cited by 38
Self-citationWu, D., Hartman, A., Ward, N. L., & Eisen, J. A. (2008) · PLoS ONE · doi:10.1371/annotation/c1aa88dd-4360-4902-8599-4d7edca79817 · Cited by 31
Stringent control in the archaeal genus Sulfolobus
Cellini, A., Scoarughi, G. L., Poggiali, P., Santino, I., Sessa, R., Donini, P., & Cimmino, C. (2003) · Research in Microbiology · doi:10.1016/j.resmic.2003.11.006 · Cited by 24
Flagged first, then by citations
Cited by
Sorted by citations
A new view of the tree of life
Hug, L. A., Baker, B. J., Anantharaman, K., Brown, C. T., Probst, A. J., Castelle, C. J., Butterfield, C. N., Hernsdorf, A. W., Amano, Y., Ise, K., et al. (2016) · Nature Microbiology · doi:10.1038/nmicrobiol.2016.48 · Cited by 2,039
Self-citationRecovery of nearly 8,000 metagenome-assembled genomes substantially expands the tree of life
Parks, D. H., Rinke, C., Chuvochina, M., Chaumeil, P.-A., Woodcroft, B. J., Evans, P. N., Hugenholtz, P., & Tyson, G. W. (2017) · Nature Microbiology · doi:10.1038/s41564-017-0012-7 · Cited by 1,882
Programmed DNA destruction by miniature CRISPR-Cas14 enzymes
Harrington, L. B., Burstein, D., Chen, J. S., Páez-Espino, D., Ma, E., Witte, I. P., Cofsky, J. C., Kyrpides, N. C., Banfield, J. F., & Doudna, J. A. (2018) · Science · doi:10.1126/science.aav4294 · Cited by 1,243
Self-citationAsgard archaea illuminate the origin of eukaryotic cellular complexity
Zaremba-Niedzwiedzka, K., Caceres, E. F., Saw, J. H., Bäckström, D., Juzokaite, L., Vancaester, E., Seitz, K. W., Anantharaman, K., Starnawski, P., Kjeldsen, K. U., et al. (2017) · Nature · doi:10.1038/nature21031 · Cited by 1,226
Self-citationUnusual biology across a group comprising more than 15% of domain Bacteria
Brown, C. T., Hug, L. A., Thomas, B. C., Sharon, I., Castelle, C. J., Singh, A., Wilkins, M. J., Wrighton, K. C., Williams, K. H., & Banfield, J. F. (2015) · Nature · doi:10.1038/nature14486 · Cited by 1,216
Self-citation
Metadata
- Authors
- Castelle, C. J., Wrighton, K. C., Thomas, B. C., Hug, L. A., Brown, C. T., Wilkins, M. J., Frischkorn, K. R., Tringe, S. G., Singh, A., Markillie, L. M., Taylor, R. C., Williams, K. H., & Banfield, J. F.
- Affiliations
- University of California, Berkeley (US)
- The Ohio State University (US)
- Lamont-Doherty Earth Observatory (US)
- Joint Genome Institute (US)
- Pacific Northwest National Laboratory (US)
- Lawrence Berkeley National Laboratory (US)
- Corresponding author
- Banfield, Jillian F.
- ORCID
- Venue
- Current Biology
- Publisher
- Elsevier BV
- Published
- 2015-03
- Volume
- 25
- Issue
- 6
- Pages
- 690-701
- ISSN
- 0960-9822 (ISSN-L)
- OpenAlex
- W2117349822
- Cited by
- 536
- References
- 72
- Citations by year
- 2026: 19 · 2025: 22 · 2024: 29 · 2023: 38 · 2022: 52 · 2021: 59 · 2020: 64 · 2019: 54 · 2018: 65 · 2017: 60 · 2016: 57 · 2015: 14
- FWCI
- 59.19
- Type
- journal article
- Language
- en
- Open access
- bronze
- doi.org
- Licence
- www.elsevier.com/tdm/userlicense/1.0/ (tdm)
- www.elsevier.com/legal/tdmrep-license (tdm)
- www.elsevier.com/open-access/userlicense/1.0/ (vor, 381 d)
- doi.org/10.15223/policy-017 (stm-asf)
- doi.org/10.15223/policy-037 (stm-asf)
- doi.org/10.15223/policy-012 (stm-asf)
- doi.org/10.15223/policy-029 (stm-asf)
- doi.org/10.15223/policy-004 (stm-asf)
- Locations
- Current Biology (publishedVersion)
- PubMed (publishedVersion)
- eScholarship (California Digital Library) (submittedVersion)
- OSTI OAI (U.S. Department of Energy Office of Scientific and Technical Information) (submittedVersion)
- Funders
- US Department of Energy (DOE), Office of Science, Office of Biological and Environmental Research (DE-AC02-05CH11231, DE-SC0004918)
- US DOE Joint Genome Institute, a DOE Office of Science User Facility (DE-AC02-05CH11231)
- DOE Office of Biological and Environmental Research
- US DOE (DE-AC06-76RLO 1830)
- Natural Sciences and Engineering Research Council of Canada postdoctoral fellowship
- Topics
- Physical Sciences › Environmental Science › Ecology › Microbial Community Ecology and Physiology
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Genomics and Phylogenetic Studies
- Physical Sciences › Environmental Science › Environmental Chemistry › Methane Hydrates and Related Phenomena
- Keywords
- genome-resolved metagenomics, fermentation, aquifer sediments, archaeal diversity
- MeSH terms
- Anaerobiosis, Archaea, Models, Biological, Models, Genetic, Phylogeny, Genome, Archaeal, Biodiversity, Metagenomics, Carbon Cycle
About these checks
Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.
Statistics and arithmetic are recomputed, not judged.
Confidence bands are shown only for fields calibrated on our annotated test set. None is calibrated yet, so no band is shown.
What counts as a claim ›How we measure confidence ›How we check this ›
Are you an author, or do you see a problem with this page? Request a review