Cited by 142Microbial Community Ecology and PhysiologyPolar Research and EcologyGenomics and Phylogenetic Studies

The DOI matches its Crossref record; 58 of the 59 references it cites were found in a registry or an index.

Diversity of Bacteroidetes in high‐altitude saline evaporitic basins in northern Chile

Open access

Dorador, Cristina, Meneses, Daniela, Urtuvia, Viviana, Demergasso, Cecilia, Vila, Irma, Witzel, Karl‐Paul, Imhoff, Johannes F.·2009·Journal of Geophysical Research: Biogeosciences

DOI 10.1029/2008jg000837

Open this paper in CoChat — free account Open PDF

Abstract

The phylum Bacteroidetes represents one of the most abundant bacterial groups of marine and freshwater bacterioplankton. We investigated the diversity of Bacteroidetes in water and sediment samples from three evaporitic basins located in the highlands of northern Chile. We used both 16S rRNA gene clone libraries created with targeted Bacteroidetes‐specific primers and separation of specifically amplified gene fragments by denaturing gradient gel electrophoresis (DGGE). DGGE analysis revealed a reduced richness of these organisms in samples from Salar de Huasco (two to four DGGE bands) increasing in Salar de Ascotán (two to seven DGGE bands) and Laguna Tebenquiche at Salar de Atacama (four to eight DGGE bands). Cluster analysis (WPGMA) of DGGE bands showed that bands from Salar de Huasco and Salar de Ascotán grouped together and samples from Salar de Atacama formed separate clusters in water and sediment samples, reflecting different Bacteroidetes communities between sites. Most of the sequences analyzed belonged to the family Flavobacteriaceae and clustered with the genera Psychroflexus, Gillisia, Maribacter, Muricauda, Flavobacterium, and Salegentibacter. The most abundant phylotype was highly related to Psychroflexus spp. and was recovered from all three study sites. The similarity of the analyzed sequences with their closest relatives in GenBank was typically <97% and notably lower when compared with type strains, demonstrating the unique character of these sequences. Culture efforts will be necessary to get a better description of the diversity of this group in saline evaporitic basins of northern Chile.

Integrity signals

Registry

Crossref · 10.1029/2008jg000837

Cites

58 of 58 references verified0 citation errors · 0 not checkable

Statistics

Recomputing p-values needs the paper’s full text.

Claims the paper makes

We couldn’t retrieve this paper’s full text, so its claims and self-check weren’t run. The registry and citation checks still apply.

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?

MEGA4: Molecular Evolutionary Genetics Analysis (MEGA) Software Version 4.0
Tamura, K., Dudley, J. T., Nei, M., & Kumar, S. (2007) · Molecular Biology and Evolution · doi:10.1093/molbev/msm092 · Cited by 28,734
Profiling of complex microbial populations by denaturing gradient gel electrophoresis analysis of polymerase chain reaction-amplified genes coding for 16S rRNA
Muyzer, G., de Waal, E. C., & Uitterlinden, A. G. (1993) · Applied and Environmental Microbiology · doi:10.1128/aem.59.3.695-700.1993 · Cited by 11,490
Taxonomic Note: A Place for DNA-DNA Reassociation and 16S rRNA Sequence Analysis in the Present Species Definition in Bacteriology
Stackebrandt, E. S., & Goebel, B. M. (1994) · INTERNATIONAL JOURNAL OF SYSTEMATIC AND EVOLUTIONARY MICROBIOLOGY · doi:10.1099/00207713-44-4-846 · Cited by 7,170
BLAST 2 Sequences, a new tool for comparing protein and nucleotide sequences
Tatusova, T. A., & Madden, T. L. (1999) · FEMS Microbiology Letters · doi:10.1111/j.1574-6968.1999.tb13575.x · Cited by 1,789
PHYML Online--a web server for fast maximum likelihood-based phylogenetic inference
Guindon, S., Lethiec, F., Duroux, P., & Gascuel, O. (2005) · Nucleic Acids Research · doi:10.1093/nar/gki352 · Cited by 1,498
Counting the Uncountable: Statistical Approaches to Estimating Microbial Diversity
Hughes, J. B., Hellmann, J. J., Ricketts, T. H., & Bohannan, B. J. M. (2001) · Applied and Environmental Microbiology · doi:10.1128/aem.67.10.4399-4406.2001 · Cited by 1,337
The ecology of Cytophaga–Flavobacteria in aquatic environments
Kirchman, D. L. (2002) · FEMS Microbiology Ecology · doi:10.1111/j.1574-6941.2002.tb00910.x · Cited by 1,307
Phylogenetic relationships of Thiomicrospira species and their identification in deep-sea hydrothermal vent samples by denaturing gradient gel electrophoresis of 16S rDNA fragments
Muyzer, G., Teske, A., Wirsen, C. O., & Jannasch, H. W. (1995) · Archives of Microbiology · doi:10.1007/bf02529967 · Cited by 1,121
Natural Assemblages of Marine Proteobacteria and Members of the Cytophaga-Flavobacter Cluster Consuming Low- and High-Molecular-Weight Dissolved Organic Matter
Cottrell, M. T., & Kirchman, D. L. (2000) · Applied and Environmental Microbiology · doi:10.1128/aem.66.4.1692-1697.2000 · Cited by 1,085
Comparative 16S rRNA Analysis of Lake Bacterioplankton Reveals Globally Distributed Phylogenetic Clusters Including an Abundant Group of Actinobacteria
Glöckner, F. O., Zaĭchikov, E. F., Belkova, N. L., Denissova, L., Pernthaler, J., Pernthaler, A., & Amann, R. (2000) · Applied and Environmental Microbiology · doi:10.1128/aem.66.11.5053-5065.2000 · Cited by 611
The Road Map to the Manual
Garrity, G. M., & Holt, J. G. (2015) · Bergey's Manual of Systematics of Archaea and Bacteria · doi:10.1002/9781118960608.bm00031 · Cited by 507
Microbial Diversity in Water and Sediment of Lake Chaka, an Athalassohaline Lake in Northwestern China
Jiang, H., Dong, H., Zhang, G., Yu, B., Chapman, L. R., & Fields, M. W. (2006) · Applied and Environmental Microbiology · doi:10.1128/aem.02869-05 · Cited by 449
Salinibacter ruber gen. nov., sp. nov., a novel, extremely halophilic member of the Bacteria from saltern crystallizer ponds.
Antón, J., Oren, A., Benlloch, S., Rodríguez‐Valera, F., Amann, R., & Rossello-Mora, R. A. (2002) · INTERNATIONAL JOURNAL OF SYSTEMATIC AND EVOLUTIONARY MICROBIOLOGY · doi:10.1099/00207713-52-2-485 · Cited by 440
Handbook of new bacterial systematics
Sneath, P. H. A. (1994) · Trends in Ecology & Evolution · doi:10.1016/0169-5347(94)90093-0 · Cited by 420
Properties of the Rarefaction Diversity Measurement
Simberloff, D. (1972) · The American Naturalist · doi:10.1086/282781 · Cited by 413
Diversity and Structure of Bacterial Communitiesin Arctic versus Antarctic PackIce
Brınkmeyer, R., Knittel, K., Jürgens, J., WEYLAND, H., Amann, R., & Helmke, E. (2003) · Applied and Environmental Microbiology · doi:10.1128/aem.69.11.6610-6619.2003 · Cited by 399
The Road Map to the Manual
Garrity, G. M., & Holt, J. G. (2001) · Springer eBooks · doi:10.1007/978-0-387-21609-6_15 · Cited by 398
Phylogenetic analysis and taxonomic study of marine Cytophaga-like bacteria: proposal for Tenacibaculum gen. nov. with Tenacibaculum maritimum comb. nov. and Tenacibaculum ovolyticum comb. nov., and description of Tenacibaculum mesophilum sp. nov. and Tenacibaculum amylolyticum sp. nov.
Suzuki, M., Nakagawa, Y., Harayama, S., & Yamamoto, S. (2001) · INTERNATIONAL JOURNAL OF SYSTEMATIC AND EVOLUTIONARY MICROBIOLOGY · doi:10.1099/00207713-51-5-1639 · Cited by 397
Depth Distribution of Microbial Diversity in Mono Lake, a Meromictic Soda Lake in California
Humayoun, S. B., Bano, N., & Hollibaugh, J. T. (2003) · Applied and Environmental Microbiology · doi:10.1128/aem.69.2.1030-1042.2003 · Cited by 381
Whole genome analysis of the marine Bacteroidetes ‘ Gramella forsetii ’ reveals adaptations to degradation of polymeric organic matter
Bauer, M., Kube, M., Teeling, H., Richter, M., Lombardot, T., Allers, E., Würdemann, C., Quast, C., Kuhl, H., Knaust, F., et al. (2006) · Environmental Microbiology · doi:10.1111/j.1462-2920.2006.01152.x · Cited by 364
The Genus Flavobacterium
Bernardet, J.-F., & Bowman, J. P. (2006) · Springer eBooks · doi:10.1007/0-387-30747-8_17 · Cited by 345
The origin of brines and salts in Chilean salars: a hydrochemical review
Risacher, F., Alonso, H., & Salazar, C. (2003) · Earth-Science Reviews · doi:10.1016/s0012-8252(03)00037-0 · Cited by 325 · cited 7×
“Bacteroidetes (together with Proteobacteria) are the most frequent groups in water and sediment samples collected from high-altitude lakes (Chilean Altiplano and Atacama Desert [Demergasso et al., 2008; Dorador, 2007; Demergasso et al., 2004]; Tibetan Plateau [Zhang et al., 2007; Jiang et al., 2007; Wu et al., 2006; J…”
BackgroundInfluential
Bacterioplankton Community Composition along a Salinity Gradient of Sixteen High-Mountain Lakes Located on the Tibetan Plateau, China
Wu, Q. L., Zwart, G., Schauer, M., Agterveld, M. P. K., & Hahn, M. W. (2006) · Applied and Environmental Microbiology · doi:10.1128/aem.00767-06 · Cited by 323
Microbial response to salinity change in Lake Chaka, a hypersaline lake on Tibetan plateau
Jiang, H., Dong, H., Yu, B., Liu, X., Li, Y., Ji, S., & Zhang, C. L. (2007) · Environmental Microbiology · doi:10.1111/j.1462-2920.2007.01377.x · Cited by 267
Algoriphagus ratkowskyi gen. nov., sp. nov., Brumimicrobium glaciale gen. nov., sp. nov., Cryomorpha ignava gen. nov., sp. nov. and Crocinitomix catalasitica gen. nov., sp. nov., novel flavobacteria isolated from various polar habitats
Bowman, J. P., Nichols, C. M., & Gibson, J. A. E. (2003) · INTERNATIONAL JOURNAL OF SYSTEMATIC AND EVOLUTIONARY MICROBIOLOGY · doi:10.1099/ijs.0.02553-0 · Cited by 243
An Introduction to the Family Flavobacteriaceae
Bernardet, J., & Nakagawa, Y. (2006) · Springer eBooks · doi:10.1007/0-387-30747-8_16 · Cited by 237
Ecological and biogeographic relationships of class Flavobacteria in the Southern Ocean
Abell, G. C. J., & Bowman, J. P. (2004) · FEMS Microbiology Ecology · doi:10.1016/j.femsec.2004.09.001 · Cited by 213
Psychroflexus torquis gen. nov., sp. nov. a psychrophilic species from Antarctic sea ice, and reclassification of Flavobacterium gondwanense (Dobson et al. 1993) as Psychroflexus gondwanense gen. nov., comb. nov.
Bowman, J. P., McCammon, S. A., Lewis, T. E., Skerratt, J., Brown, J., Nichols, D. S., & McMeekin, T. A. (1998) · Microbiology · doi:10.1099/00221287-144-6-1601 · Cited by 196
Distribution of prokaryotic genetic diversity in athalassohaline lakes of the Atacama Desert, Northern Chile
Demergasso, C. S., Casamayor, E. O., Chong, G., Galleguillos, P. A., Escudero, L. V., & Pedrós‐Alió, C. (2004) · FEMS Microbiology Ecology · doi:10.1016/j.femsec.2003.12.013 · Cited by 187
Self-citation
Diverse Responses to UV-B Radiation and Repair Mechanisms of Bacteria Isolated from High-Altitude Aquatic Environments
Zenoff, V. F., Siñeriz, F., & Farı́as, M. E. (2006) · Applied and Environmental Microbiology · doi:10.1128/aem.01333-06 · Cited by 177
Interactions between marine bacteria and axenic diatoms (Cylindrotheca fusiformis, Nitzschia laevis, and Thalassiosira weissflogii) incubated under various conditions in the lab
Grossart, H. (1999) · Aquatic Microbial Ecology · doi:10.3354/ame019001 · Cited by 176
Deleya halophila, a New Species of Moderately Halophilic Bacteria
Quesada, E., Ventosa, A., Ruiz‐Berraquero, F., & Alberto Ramos-cormenzana, A. (1984) · International Journal of Systematic Bacteriology · doi:10.1099/00207713-34-3-287 · Cited by 173
Novel members of the family Flavobacteriaceae from Antarctic maritime habitats including Subsaximicrobium wynnwilliamsii gen. nov., sp. nov., Subsaximicrobium saxinquilinus sp. nov., Subsaxibacter broadyi gen. nov., sp. nov., Lacinutrix copepodicola gen. nov., sp. nov., and novel species of the genera Bizionia, Gelidibacter and Gillisia
Bowman, J. P., & Nichols, D. S. (2005) · INTERNATIONAL JOURNAL OF SYSTEMATIC AND EVOLUTIONARY MICROBIOLOGY · doi:10.1099/ijs.0.63527-0 · Cited by 164
Microbial Diversity in Sediments of Saline Qinghai Lake, China: Linking Geochemical Controls to Microbial Ecology
Dong, H., Zhang, G., Jiang, H., Yu, B., Chapman, L. R., Lucas, C. R., & Fields, M. W. (2006) · Microbial Ecology · doi:10.1007/s00248-005-0228-6 · Cited by 160
Novelty and spatio–temporal heterogeneity in the bacterial diversity of hypersaline Lake Tebenquiche (Salar de Atacama)
Demergasso, C. S., Escudero, L. V., Casamayor, E. O., Chong, G., Balagué, V., & Pedrós‐Alió, C. (2008) · Extremophiles · doi:10.1007/s00792-008-0153-y · Cited by 129
Self-citation
The microbial composition of three limnologically disparate hypersaline Antarctic lakes
Bowman, J. P., McCammon, S. A., Rea, S. M., & McMeekin, T. A. (2000) · FEMS Microbiology Letters · doi:10.1111/j.1574-6968.2000.tb08937.x · Cited by 120
Maribacter gen. nov., a new member of the family Flavobacteriaceae, isolated from marine habitats, containing the species Maribacter sedimenticola sp. nov., Maribacter aquivivus sp. nov., Maribacter orientalis sp. nov. and Maribacter ulvicola sp. nov.
Nedashkovskaya, O. I., Kim, S. B., Han, S. K., Lysenko, A. M., Rohde, M., Rhee, M.-S., Frolova, G. M., Falsen, E., Mikhailov, V. V., & Bae, K. S. (2004) · INTERNATIONAL JOURNAL OF SYSTEMATIC AND EVOLUTIONARY MICROBIOLOGY · doi:10.1099/ijs.0.02849-0 · Cited by 116
Diversity of Aerobic Methanotrophic Bacteria in a Permafrost Active Layer Soil of the Lena Delta, Siberia
Liebner, S., Rublack, K., Stührmann, T., & Wagner, D. (2008) · Microbial Ecology · doi:10.1007/s00248-008-9411-x · Cited by 112
Prolixibacter bellariivorans gen. nov., sp. nov., a sugar-fermenting, psychrotolerant anaerobe of the phylum Bacteroidetes, isolated from a marine-sediment fuel cell
Holmes, D. E., Nevin, K. P., Woodard, T. L., Peacock, A. D., & Lovley, D. R. (2007) · INTERNATIONAL JOURNAL OF SYSTEMATIC AND EVOLUTIONARY MICROBIOLOGY · doi:10.1099/ijs.0.64296-0 · Cited by 111
Microbial diversity of benthic mats along a tidal desiccation gradient
Rothrock, M. J., & García‐Pichel, F. (2005) · Environmental Microbiology · doi:10.1111/j.1462-2920.2005.00728.x · Cited by 106
The Phylogeny and Signature Sequences Characteristics ofFibrobacteres,Chlorobi, andBacteroidetes
Gupta, R. S. (2004) · Critical Reviews in Microbiology · doi:10.1080/10408410490435133 · Cited by 104
Direct Sequencing of the Polymerase Chain Reaction-Amplified 16S rRNA Gene of Flavobacterium gondwanense sp. nov. and Flavobacterium salegens sp. nov., Two New Species from a Hypersaline Antarctic Lake
Dobson, S. J., Colwell, R. R., McMeekin, T., & Franzmann, P. D. (1993) · International Journal of Systematic Bacteriology · doi:10.1099/00207713-43-1-77 · Cited by 103
Owenweeksia hongkongensis gen. nov., sp. nov., a novel marine bacterium of the phylum ‘Bacteroidetes’
Lau, K. W. K., Ng, C. Y. M., Ren, J., Lau, S. C. L., Qian, P., Wong, P. K., Lau, T. C., & Wu, M. C. S. (2005) · INTERNATIONAL JOURNAL OF SYSTEMATIC AND EVOLUTIONARY MICROBIOLOGY · doi:10.1099/ijs.0.63155-0 · Cited by 90
Microbial community structure in moraine lakes and glacial meltwaters, Mount Everest
Liu, Y., Yao, T., Jiao, N., Kang, S., Zeng, Y., & Huang, S. (2006) · FEMS Microbiology Letters · doi:10.1111/j.1574-6968.2006.00477.x · Cited by 82
Cyanobacterial diversity in Salar de Huasco, a high altitude saline wetland in northern Chile: an example of geographical dispersion?
Dorador, C., Vila, I., Imhoff, J. F., & Witzel, K. (2008) · FEMS Microbiology Ecology · doi:10.1111/j.1574-6941.2008.00483.x · Cited by 73
Self-citation
Psychroflexus tropicus sp. nov., an obligately halophilic Cytophaga–Flavobacterium–Bacteroides group bacterium from an Hawaiian hypersaline lake
Donachie, S. P., Bowman, J. P., & Alam, M. S. (2004) · INTERNATIONAL JOURNAL OF SYSTEMATIC AND EVOLUTIONARY MICROBIOLOGY · doi:10.1099/ijs.0.02733-0 · Cited by 65
Muricauda flavescens sp. nov. and Muricauda aquimarina sp. nov., isolated from a salt lake near Hwajinpo Beach of the East Sea in Korea, and emended description of the genus Muricauda
Yoon, J., Lee, M., Oh, T.-K., & Park, Y.-H. (2005) · INTERNATIONAL JOURNAL OF SYSTEMATIC AND EVOLUTIONARY MICROBIOLOGY · doi:10.1099/ijs.0.03051-0 · Cited by 63
Gillisia limnaea gen. nov., sp. nov., a new member of the family Flavobacteriaceae isolated from a microbial mat in Lake Fryxell, Antarctica
Trappen, S. V., Vandecandelaere, I., Mergaert, J., & Swings, J. (2004) · INTERNATIONAL JOURNAL OF SYSTEMATIC AND EVOLUTIONARY MICROBIOLOGY · doi:10.1099/ijs.0.02922-0 · Cited by 62
Phylogenetic diversity of bacteria isolates from the Qinghai-Tibet Plateau permafrost region
Zhang, G., Niu, F., Ma, X., Liu, W., Dong, M., Feng, H., An, L., & Cheng, G. (2007) · Canadian Journal of Microbiology · doi:10.1139/w07-031 · Cited by 57
Trends in the Water Chemistry of High Altitude Lakes in Europe
MOSELLO, R., Lami, A., Marchetto, A., Rogora, M., Wathne, B., Lien, L., Catalán, J., Camarero, L., Ventura, M., Psenner, R., et al. (2002) · Water Air and Soil Pollution Focus · doi:10.1023/a:1020138221582 · Cited by 48
Molecular analysis of enrichment cultures of ammonia oxidizers from the Salar de Huasco, a high altitude saline wetland in northern Chile
Dorador, C., Busekow, A., Vila, I., Imhoff, J. F., & Witzel, K. (2008) · Extremophiles · doi:10.1007/s00792-008-0146-x · Cited by 48
Self-citation
Microbial Diversity in Water and Sediment of Lake Chaka, an Athalassohaline Lake in Northwestern China
Jiang, H., Dong, H., Zhang, G., Yu, B., Chapman, L. R., & Fields, M. W. (2006) · Applied and Environmental Microbiology · doi:10.1128/aem.02230-06 · Cited by 47
The Marine Clade of the Family Flavobacteriaceae: The Genera Aequorivita, Arenibacter, Cellulophaga, Croceibacter, Formosa, Gelidibacter, Gillisia, Maribacter, Mesonia, Muricauda, Polaribacter, Psychroflexus, Psychroserpens, Robiginitalea, Salegentibacter, Tenacibaculum, Ulvibacter, Vitellibacter and Zobellia
(14732239), J. B. (2011) · SpringerReference · doi:10.1007/springerreference_3876 · Cited by 40
A limnological reconnaissance of Lake Tebenquiche, Salar de Atacama, Chile
Zúñiga, L. R., Campos, V., Pinochet, H., & Prado, B. (1991) · Hydrobiologia · doi:10.1007/bf00014320 · Cited by 40
Depth-specific distribution of Bacteroidetes in the oligotrophic Eastern Mediterranean Sea
Blümel, M., Süling, J., & Imhoff, J. (2007) · Aquatic Microbial Ecology · doi:10.3354/ame046209 · Cited by 28
Self-citation
Psychroserpens mesophilus sp. nov., a mesophilic marine bacterium belonging to the family Flavobacteriaceae isolated from a young biofilm
Kwon, K. K., Lee, S. J., Park, J. H., Ahn, T., & Lee, H. K. (2006) · INTERNATIONAL JOURNAL OF SYSTEMATIC AND EVOLUTIONARY MICROBIOLOGY · doi:10.1099/ijs.0.64171-0 · Cited by 24
Microbial diversity in sediments of saline Qinghai Lake, China： Linking geochemical controls to microbial ecology
Dong, Hl, Zhang, Gx, Jiang, Hc, Yu, Bs, Chapman, Lr, et al. (2007) · 中国生物学文摘 · Cited by 22
Microbial communities in high altitude altiplanic wetlands in northern Chile: phylogeny, diversity and function
Ortiz, D., & Cristina, I. (2007) · Helmholtz Centre for Ocean Research Kiel (GEOMAR) · Cited by 16

Research works printed but not linked: 3

10.1007/0-387-30747-8_17 · DOI
10.1007/0-387-30747-8_17 · DOI
Vila I., 1987, Dinámica de lagos de altura, perspectivas de investigación, Arch. Biol. Med. Exp. (Santiago), 20, 95

Sorted by citations

Bacterial community structure in simultaneous nitrification, denitrification and organic matter removal process treating saline mustard tuber wastewater as revealed by 16S rRNA sequencing
Wang, J., Gong, B., Huang, W., Wang, Y., & Zhou, J. (2016) · Bioresource Technology · doi:10.1016/j.biortech.2016.12.071 · Cited by 186
Metagenomic insights into salinity effect on diversity and abundance of denitrifying bacteria and genes in an expanded granular sludge bed reactor treating high-nitrate wastewater
Miao, Y., Liao, R., Zhang, X., Liu, B., Li, Y., Wu, B., & Li, A. (2015) · Chemical Engineering Journal · doi:10.1016/j.cej.2015.04.125 · Cited by 142
The discovery of stromatolites developing at 3570 m above sea level in a high-altitude volcanic Lake Socompa, Argentinean Andes
Farías, M. E., Rascovan, N., Toneatti, D. M., Albarracín, V. H., Flores, M. R., Poiré, D. G., Collavino, M. M., Aguilar, O. M., Vazquez, M. P., & Polerecky, L. (2013) · PLoS ONE · doi:10.1371/journal.pone.0053497 · Cited by 133
Characterization of bacterial diversity associated with microbial mats, gypsum evaporites and carbonate microbialites in thalassic wetlands: Tebenquiche and La Brava, Salar de Atacama, Chile
Farías, M. E., Contreras, M., Rasuk, M. C., Kurth, D., Flores, M. R., Poiré, D. G., Novoa, F., & Visscher, P. T. (2014) · Extremophiles · doi:10.1007/s00792-013-0617-6 · Cited by 125
Composition and distribution of microbial communities in natural river wetlands and corresponding constructed wetlands
Cao, Q., Wang, H., Chen, X., Wang, R., & Liu, J. (2016) · Ecological Engineering · doi:10.1016/j.ecoleng.2016.10.063 · Cited by 112

See all 142

Authors: Dorador, C., Meneses, D., Urtuvia, V., Demergasso, C., Vila, I., Witzel, K., & Imhoff, J. F.
Affiliations: Max Planck Society (DE)
Universidad Católica del Norte (CL)
University of Chile (CL)
Max Planck Institute for Evolutionary Biology (DE)
GEOMAR Helmholtz Centre for Ocean Research Kiel (DE)
ORCID: Dorador, Cristina
Urtuvia, Viviana
Demergasso, Cecilia
Vila, Irma
Imhoff, Johannes F.
Venue: Journal of Geophysical Research: Biogeosciences
Publisher: American Geophysical Union (AGU)
Published: 2009-06
Volume: 114
Issue: G2
ISSN: 0148-0227 (ISSN-L)
DOI: 10.1029/2008jg000837
OpenAlex: W2072582771
Cited by: 142
References: 59
Citations by year: 2026: 3 · 2025: 4 · 2024: 22 · 2023: 42 · 2022: 2 · 2021: 7 · 2020: 12 · 2019: 5 · 2018: 9 · 2017: 6 · 2016: 8 · 2015: 9 · 2014: 2 · 2013: 4 · 2012: 1
FWCI: 2.04
Type: journal article
Language: en
Open access: green
oceanrep.geomar.de
Licence: other-oa
onlinelibrary.wiley.com/termsAndConditions#vor (vor, 88 d)
Locations: Journal of Geophysical Research Atmospheres (publishedVersion)
Helmholtz Centre for Ocean Research Kiel (GEOMAR) (acceptedVersion, other-oa)
Max Planck Institute for Plasma Physics (submittedVersion)
MPG.PuRe (Max Planck Society) (submittedVersion)
Funders: Deutscher Akademischer Austauschdienst
Comisión Nacional de Investigación Científica y Tecnológica
Topics: Physical Sciences › Environmental Science › Ecology › Microbial Community Ecology and Physiology
Physical Sciences › Environmental Science › Ecology › Polar Research and Ecology
Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Genomics and Phylogenetic Studies
Keywords: Bacteroidetes, bacterial diversity, high-altitude lakes, Salar de Atacama, Flavobacteriaceae, bacterial communities, 16S rRNA gene, saline lakes, northern Chile

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

Diversity of Bacteroidetes in high‐altitude saline evaporitic basins in northern Chile

Abstract

Overview

Integrity signals

Verification

Claims the paper makes

Claims other papers make about this one

Citations

Cites

Cited by

Related

Metadata

Record

About these checks