Microbial turnover times in the deep seabed studied by amino acid racemization modelling

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Microbial turnover times in the deep seabed studied by amino acid racemization modelling is …
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P6179Dimensions Publication ID1090696251
P356DOI10.1038/S41598-017-05972-Z
P932PMC publication ID5516024
P698PubMed publication ID28720809

P50authorMarit-Solveig SeidenkrantzQ53977006
Christof PearceQ58181937
Hans RøyQ60393363
Kasper Urup KjeldsenQ79969913
Bo Barker JørgensenQ95239175
P2093author name stringBente Aa Lomstein
Stefan Braun
Marion Jaussi
Snehit S Mhatre
P2860cites workCorrection: Abiotic racemization kinetics of amino acids in marine sedimentsQ43224695
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Aspartic acid racemization and age-depth relationships for organic carbon in Siberian permafrostQ44227820
Does aspartic acid racemization constrain the depth limit of the subsurface biosphere?Q44556681
Preservation of organic matter in marine sediments: controls, mechanisms, and an imbalance in sediment organic carbon budgets?Q44926488
Isoleucine epimerization in peptides and proteins: kinetic factors and application to fossil proteinsQ47640484
Aerobic microbial respiration in 86-million-year-old deep-sea red clay.Q50510799
Group-specific primer and probe sets to detect methanogenic communities using quantitative real-time polymerase chain reaction.Q51543613
Bayesian Analysis of Radiocarbon DatesQ54864766
New cell extraction procedure applied to deep subsurface sedimentsQ56973600
Distributions of Microbial Activities in Deep Subseafloor SedimentsQ56973627
Prokaryotic cells of the deep sub-seafloor biosphere identified as living bacteriaQ57087955
Racemization of amino acids in marine sedimentsQ57088768
Deposition models for chronological recordsQ57262905
Racemization of Amino Acids in NatureQ58437536
Endospore abundance, microbial growth and necromass turnover in deep sub-seafloor sedimentQ59076277
Early diagenesis of organic matter in marine sediments: progress and perplexityQ60308492
High performance liquid chromatographic determination of subpicomole amounts of amino acids by precolumn fluorescence derivatization with o-phthaldialdehydeQ62475285
Kinetics of amino acid racemization in Sequoiadendron giganteum heartwoodQ67683136
Survival and Activity of Bacteria in a Deep, Aged Lake Sediment (Lake Constance)Q73087864
Effect of temperature on sulphate reduction, growth rate and growth yield in five psychrophilic sulphate-reducing bacteria from Arctic sedimentsQ73510867
Spore dipicolinic acid contents used for estimating the number of endospores in sedimentsQ80594296
Prokaryotes: the unseen majorityQ22066200
IntCal13 and Marine13 Radiocarbon Age Calibration Curves 0–50,000 Years cal BPQ22255462
Abiotic racemization kinetics of amino acids in marine sedimentsQ28683516
Heterotrophic Archaea dominate sedimentary subsurface ecosystems off PeruQ28768174
Desulfobacter psychrotolerans sp. nov., a new psychrotolerant sulfate-reducing bacterium and descriptions of its physiological response to temperature changesQ31023490
Vertical profiles of methanogenesis and methanogens in two contrasting acidic peatlands in central New York State, USA.Q33251974
Diversity of sulfur isotope fractionations by sulfate-reducing prokaryotesQ33988950
Mutations enhancing amino acid catabolism confer a growth advantage in stationary phaseQ33992996
Global distribution of microbial abundance and biomass in subseafloor sedimentQ34296356
DEEP BIOSPHERE. Exploring deep microbial life in coal-bearing sediment down to ~2.5 km below the ocean floor.Q34486690
Diversity of sulfate-reducing bacteria from an extreme hypersaline sediment, Great Salt Lake (Utah).Q34609479
Survival of prokaryotes in a polluted waste dump during remediation by alkaline hydrolysisQ35095148
Deep subseafloor microbial cells on physiological standby.Q35546698
Viral activities and life cycles in deep subseafloor sediments.Q35673738
Power limits for microbial lifeQ35852345
Formate, acetate, and propionate as substrates for sulfate reduction in sub-arctic sediments of Southwest GreenlandQ35989205
Long-term survival during stationary phase: evolution and the GASP phenotypeQ36369839
Dispersal of thermophilic Desulfotomaculum endospores into Baltic Sea sediments over thousands of yearsQ36472358
Size and Carbon Content of Sub-seafloor Microbial Cells at Landsort Deep, Baltic Sea.Q37218256
Intragenomic heterogeneity of 16S rRNA genes causes overestimation of prokaryotic diversityQ37263616
Microbial life under extreme energy limitation.Q38074264
Environmental roles of microbial amino acid racemases.Q38595346
Microbial community assembly and evolution in subseafloor sediment.Q38938702
Community size and metabolic rates of psychrophilic sulfate-reducing bacteria in Arctic marine sediments.Q39527947
A critical evaluation of the application of amino acid racemization to geochronology and geothermometryQ39709399
Meta-analysis of quantification methods shows that archaea and bacteria have similar abundances in the subseafloorQ42060759
Ion permeability of the cytoplasmic membrane limits the maximum growth temperature of bacteria and archaeaQ43024161
P275copyright licenseCreative Commons Attribution 4.0 InternationalQ20007257
P6216copyright statuscopyrightedQ50423863
P433issue1
P407language of work or nameEnglishQ1860
P304page(s)5680
P577publication date2017-07-18
P1433published inScientific ReportsQ2261792
P1476titleMicrobial turnover times in the deep seabed studied by amino acid racemization modelling
P478volume7

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