Preserved particulate organic carbon is likely derived from the subsurface sulfidic photic zone of the Proterozoic Ocean: evidence from a modern, oxygen-deficient lake
Ashley B. Cohen, Lisa N. Christensen, Felix Weber, Milana Yagudaeva, Evan Lo, Gregory A. Henkes, Michael L. McCormick, Gordon T. Taylor
{"title":"Preserved particulate organic carbon is likely derived from the subsurface sulfidic photic zone of the Proterozoic Ocean: evidence from a modern, oxygen-deficient lake","authors":"Ashley B. Cohen, Lisa N. Christensen, Felix Weber, Milana Yagudaeva, Evan Lo, Gregory A. Henkes, Michael L. McCormick, Gordon T. Taylor","doi":"10.1111/gbi.12593","DOIUrl":null,"url":null,"abstract":"<p>Biological processes in the Proterozoic Ocean are often inferred from modern oxygen-deficient environments (MODEs) or from stable isotopes in preserved sediment. To date, few MODE studies have simultaneously quantified carbon fixation genes and attendant stable isotopic signatures. Consequently, how carbon isotope patterns reflect these pathways has not been thoroughly vetted. Addressing this, we profiled planktonic productivity and quantified carbon fixation pathway genes and associated organic carbon isotope values (δ<sup>13</sup>C<sub>POC</sub>) of size-fractionated (0.2–2.7 and >2.7 μm) particulate matter from meromictic Fayetteville Green Lake, NY, USA. The high-O<sub>2</sub> Calvin-Benson-Bassham (CBB) gene (<i>cbbL</i>) was most abundant in the <2.7 μm size fraction in shallow oxic and deep hypoxic waters, corresponding with cyanobacterial and eukaryote algal populations. The low-O<sub>2</sub> CBB gene (<i>cbbM</i>) was most abundant near the lower oxycline boundary in the larger size fraction, coincident with purple sulfur bacteria populations. The reverse citric acid cycle gene (<i>aclB</i>) was equally abundant in both size fractions in the deepest photic zone, coinciding with green sulfur bacteria populations. Methane coenzyme reductase A (<i>mcrA</i>), of anaerobic methane cyclers, was most abundant at the lower oxycline boundary in both size fractions, coinciding with <i>Methanoregula</i> populations. δ<sup>13</sup>C<sub>POC</sub> values overlapped with the high-O<sub>2</sub> CBB fixation range except for two negative excursions near the lower oxycline boundary, likely reflecting assimilation of isotopically-depleted groundwater-derived carbon by autotrophs and sulfate-reducers. Throughout aphotic waters, δ<sup>13</sup>C<sub>POC</sub> values of the large size fraction became <sup>13</sup>C-enriched, likely reflecting abundant purple sulfur bacterial aggregates. Eukaryote algae- or cyanobacteria-like isotopic signatures corresponded with increases in <i>cbbL</i>, <i>cbbM,</i> and <i>aclB</i>, and enrichment of exopolymer-rich prokaryotic photoautotrophs aggregates. Results suggest that δ<sup>13</sup>C<sub>POC</sub> values of preserved sediments from areas of the Proterozoic Ocean with sulfidic photic zones may reflect a mixture of alternate carbon-fixing populations exported from the deep photic zone, challenging the paradigm that sedimentary stable carbon isotope values predominantly reflect oxygenic photosynthesis from surface waters.</p>","PeriodicalId":173,"journal":{"name":"Geobiology","volume":"22 2","pages":""},"PeriodicalIF":2.7000,"publicationDate":"2024-03-12","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Geobiology","FirstCategoryId":"89","ListUrlMain":"https://onlinelibrary.wiley.com/doi/10.1111/gbi.12593","RegionNum":2,"RegionCategory":"地球科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"BIOLOGY","Score":null,"Total":0}
引用次数: 0
Abstract
Biological processes in the Proterozoic Ocean are often inferred from modern oxygen-deficient environments (MODEs) or from stable isotopes in preserved sediment. To date, few MODE studies have simultaneously quantified carbon fixation genes and attendant stable isotopic signatures. Consequently, how carbon isotope patterns reflect these pathways has not been thoroughly vetted. Addressing this, we profiled planktonic productivity and quantified carbon fixation pathway genes and associated organic carbon isotope values (δ13CPOC) of size-fractionated (0.2–2.7 and >2.7 μm) particulate matter from meromictic Fayetteville Green Lake, NY, USA. The high-O2 Calvin-Benson-Bassham (CBB) gene (cbbL) was most abundant in the <2.7 μm size fraction in shallow oxic and deep hypoxic waters, corresponding with cyanobacterial and eukaryote algal populations. The low-O2 CBB gene (cbbM) was most abundant near the lower oxycline boundary in the larger size fraction, coincident with purple sulfur bacteria populations. The reverse citric acid cycle gene (aclB) was equally abundant in both size fractions in the deepest photic zone, coinciding with green sulfur bacteria populations. Methane coenzyme reductase A (mcrA), of anaerobic methane cyclers, was most abundant at the lower oxycline boundary in both size fractions, coinciding with Methanoregula populations. δ13CPOC values overlapped with the high-O2 CBB fixation range except for two negative excursions near the lower oxycline boundary, likely reflecting assimilation of isotopically-depleted groundwater-derived carbon by autotrophs and sulfate-reducers. Throughout aphotic waters, δ13CPOC values of the large size fraction became 13C-enriched, likely reflecting abundant purple sulfur bacterial aggregates. Eukaryote algae- or cyanobacteria-like isotopic signatures corresponded with increases in cbbL, cbbM, and aclB, and enrichment of exopolymer-rich prokaryotic photoautotrophs aggregates. Results suggest that δ13CPOC values of preserved sediments from areas of the Proterozoic Ocean with sulfidic photic zones may reflect a mixture of alternate carbon-fixing populations exported from the deep photic zone, challenging the paradigm that sedimentary stable carbon isotope values predominantly reflect oxygenic photosynthesis from surface waters.
期刊介绍:
The field of geobiology explores the relationship between life and the Earth''s physical and chemical environment. Geobiology, launched in 2003, aims to provide a natural home for geobiological research, allowing the cross-fertilization of critical ideas, and promoting cooperation and advancement in this emerging field. We also aim to provide you with a forum for the rapid publication of your results in an international journal of high standing. We are particularly interested in papers crossing disciplines and containing both geological and biological elements, emphasizing the co-evolutionary interactions between life and its physical environment over geological time.
Geobiology invites submission of high-quality articles in the following areas:
Origins and evolution of life
Co-evolution of the atmosphere, hydrosphere and biosphere
The sedimentary rock record and geobiology of critical intervals
Paleobiology and evolutionary ecology
Biogeochemistry and global elemental cycles
Microbe-mineral interactions
Biomarkers
Molecular ecology and phylogenetics.