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| - Corresponding Author - | | - Corresponding Author - |
| Anna\",\"lastname\":\"Cutmore\",\"orcid\":null,\"affiliation\":\"Royal | | Anna\",\"lastname\":\"Cutmore\",\"orcid\":null,\"affiliation\":\"Royal |
| Netherlands Institute for Sea | | Netherlands Institute for Sea |
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| Cutmore - Royal Netherlands Institute for Sea Research - ORCID: | | Cutmore - Royal Netherlands Institute for Sea Research - ORCID: |
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| Netherlands Institute for Sea | | Netherlands Institute for Sea |
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| Hennekam - Royal Netherlands Institute for Sea Research - ORCID: | | Hennekam - Royal Netherlands Institute for Sea Research - ORCID: |
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| Netherlands Institute for Sea | | Netherlands Institute for Sea |
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| Hopmans - Royal Netherlands Institute for Sea Research - ORCID: | | Hopmans - Royal Netherlands Institute for Sea Research - ORCID: |
| \"},{\"firstname\":\"Marcel\",\"lastname\":\"van der | | \"},{\"firstname\":\"Marcel\",\"lastname\":\"van der |
| Meer\",\"orcid\":null,\"affiliation\":\"Royal Netherlands Institute | | Meer\",\"orcid\":null,\"affiliation\":\"Royal Netherlands Institute |
| for Sea | | for Sea |
| ndingauthor\":null,\"contactemailaddress\":null,\"formatted\":\"Marcel | | ndingauthor\":null,\"contactemailaddress\":null,\"formatted\":\"Marcel |
| van der Meer - Royal Netherlands Institute for Sea Research - ORCID: | | van der Meer - Royal Netherlands Institute for Sea Research - ORCID: |
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| ndingauthor\":null,\"contactemailaddress\":null,\"formatted\":\"Meryem | | ndingauthor\":null,\"contactemailaddress\":null,\"formatted\":\"Meryem |
| Moijtahid - University of Angers - ORCID: | | Moijtahid - University of Angers - ORCID: |
| ,\"lastname\":\"Jorissen\",\"orcid\":null,\"affiliation\":\"University | | ,\"lastname\":\"Jorissen\",\"orcid\":null,\"affiliation\":\"University |
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| ondingauthor\":null,\"contactemailaddress\":null,\"formatted\":\"Frans | | ondingauthor\":null,\"contactemailaddress\":null,\"formatted\":\"Frans |
| Jorissen - University of Angers - ORCID: | | Jorissen - University of Angers - ORCID: |
| "Nicole\",\"lastname\":\"Bale\",\"orcid\":null,\"affiliation\":\"Royal | | "Nicole\",\"lastname\":\"Bale\",\"orcid\":null,\"affiliation\":\"Royal |
| Netherlands Institute for Sea | | Netherlands Institute for Sea |
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| ingauthor\":null,\"contactemailaddress\":null,\"formatted\":\"Gert-Jan | | ingauthor\":null,\"contactemailaddress\":null,\"formatted\":\"Gert-Jan |
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| Institute for Sea | | Institute for Sea |
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| "dataset_persistent_id": "DOI:10.25850/nioz/7b.b.fd", | | "dataset_persistent_id": "DOI:10.25850/nioz/7b.b.fd", |
| "deposit_date": "2022-09-14", | | "deposit_date": "2022-09-14", |
| "depositor": "Zoe van Kemenade", | | "depositor": "Zoe van Kemenade", |
| "distribution_date": "2022-09-14", | | "distribution_date": "2022-09-14", |
| "distributor": "Research Data Management(NIOZ Royal Netherlands | | "distributor": "Research Data Management(NIOZ Royal Netherlands |
| Institute for Sea Research)", | | Institute for Sea Research)", |
| "doi_date_published": "2023-03-15", | | "doi_date_published": "2023-03-15", |
| "funding_references": "[{\"name\":\"Soehngen Institute of Anaerobic | | "funding_references": "[{\"name\":\"Soehngen Institute of Anaerobic |
| Microbiology | | Microbiology |
| \",\"awardnumber\":\"024.002.002\",\"awardtitle\":\"Gravitation | | \",\"awardnumber\":\"024.002.002\",\"awardtitle\":\"Gravitation |
| Grant\"}]", | | Grant\"}]", |
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| "metadata_created": "2024-10-22T11:47:11.843489", | | "metadata_created": "2024-10-22T11:47:11.843489", |
| n | "metadata_modified": "2024-10-22T17:12:22.283710", | n | "metadata_modified": "2024-10-22T17:12:22.600381", |
| "name": "7bbfd", | | "name": "7bbfd", |
| n | "notes": "In the eastern Mediterranean Sea (EMS), the organic-poor | n | "notes": "The eastern Mediterranean Sea (EMS) sedimentary record is |
| sedimentary record is periodically interspersed with organic-rich | | periodically interspersed with organic- rich \u2018sapropel\u2019 |
| layers, known as sapropels. Sapropels are characteristic of basin-wide | | layers. Sapropels are characteristic of basin-wide anoxic events, |
| anoxic events, triggered by precession-forced insolation maxima. In | | triggered by precession-forced insolation maxima. Relatively subdued |
| the late Quaternary, relatively subdued insolation maxima are not | | insolation maxima, however, are not always expressed as distinct |
| always expressed as distinct sapropels. Late Quaternary EMS | | sapropel events. The EMS sedimentary record hereby allows anoxia and |
| sedimentary records hereby offer the opportunity to investigate | | nitrogen (N) cycling tipping points to be investigated, which may act |
| tipping points of anoxia and associated nitrogen (N) cycling dynamics. | | as analogues for modern deoxygenation. To this end, we investigated a |
| To this extent, we have investigated a ~68 kyr sediment record from | | ~68 kyr EMS sedimentary record, containing the well-established |
| the EMS (64PE406-E1), which contains the well-established Holocene | | |
| sapropel S1 (deposited in two parts: S1a [~10.5\u25008.5 kyr BP] and | | sapropel S1 (deposited in two phases: S1a [~10.5\u25008.5 ka BP] and |
| S1b [~7.8\u25006.1 kyr BP]) and the sediments timed to the ambiguous | | S1b [~7.8\u25006.1 ka BP]) and sediments timed to the ambiguous S2 |
| S2 sapropel of the late Pleistocene (~53 kyr BP). We focus on lipid | | sapropel (~53 ka BP). We focus on lipid biomarkers of microorganisms |
| biomarkers of microorganisms to reconstruct changes in key components | | to reconstruct key components of the N cycle: (1) anaerobic ammonium |
| of the N cycle: (1) anaerobic ammonium oxidation (anammox) using | | oxidation (anammox) using ladderanes and a stereoisomer of |
| ladderanes and a stereoisomer of bacteriohopanetetrol (BHT-x), (2) | | bacteriohopanetetrol (BHT-x), (2) dinitrogen gas (N2) fixation using |
| dinitrogen gas (N2) fixation using heterocyte glycolipids (HGs), and | | heterocyte glycolipids (HGs), and (3) nitrification by Thaumarchaeota |
| (3) nitrification by Thaumarchaeota using crenarchaeol. Elevated | | using crenarchaeol. During S1, export-productivity (indicated by the |
| crenarchaeol at the start of S1a indicates enhanced nitrification by | | barium to aluminum ratio) and anoxia (indicated by redox-sensitive |
| Thaumarchaeota, likely promoted by an influx of nutrients via enhanced | | trace elements and benthic foraminifer assemblages) are enhanced. |
| river discharge. Anammox occurred throughout S1, but was most intense | | Thaumarchaeota are most abundant in S1a, while anammox is enhanced |
| ~1.5 kyr after the onset of anoxia (at ~10.5 cal. kyr BP; as | | throughout S1. N2-fixation (indicated by bulk sedimentary \u03b415N) |
| indicated by redox-sensitive trace elements and benthic foraminifer | | occurs throughout S1, while the highest heterocyte cyanobacteria |
| assemblages). High organic carbon levels in S1a likely resulted in | | abundance is at the S1a termination and S1 interval. Ladderane |
| anammox being initially outcompeted by heterotrophic denitrification. | | presence suggests additional episodes of bioavailable N removal |
| N2-fixation by heterocytous cyanobacteria appeared predominantly at | | between ~69 to 39 cal ka BP. These episodes correspond to brief |
| the S1a termination and in the S1 interruption. Ladderanes suggest | | periods of water column deoxygenation, with anoxia occurring at the |
| additional episodes of bioavailable N removal between ~69 to 39 cal. | | sediment-water interface in sediments timed to S2 (53\u250051 cal ka |
| kyr BP. These episodes correspond to brief periods of anoxia at the | | BP). During these episodes, ladderanes co-occur with the BHT-34R |
| sediment-water interface, with maximum deoxygenation occurring in | | stereoisomer, but not BHT-x. Compound-specific \u03b413CBHT-34R |
| sediments timed to S2 (53\u250053 cal. kyr BP; as indicated by Mn/Al | | indicates an anammox source. Our results highlight various modes of |
| and benthic foraminifera). During these episodes, BHT-x is absent, | | operation of the N cycle during the different deoxygenation events. |
| but, ladderanes co-occur with a later eluting BHT stereoisomer | | During S1a, a combination of N-loss and P-supply may have reinforced |
| (BHT-34R). BHT-34R compound-specific \u03b413C values indicate an | | anoxia, by favoring diatom-diazotroph symbiotic consortia. Conversely, |
| anammox source, potentially synthesized by relatively poorly studied | | a coupling between N2-fixation and anammox was not observed during |
| marine sedimentary anammox bacteria. Taken all together, our results | | S1b and the S2-timed interval, either because loss of bioavailable N |
| highlight various modes of operation of the N cycle during the | | was insufficient or diazotrophs were nutrient limited. During these |
| different deoxygenation events. During S1a, a combination of anammox, | | periods, anammox may have provided negative feedback on anoxia by |
| denitrification and an excess supply of P may have been a reinforcing | | quenching primary production.", |
| feedback for anoxia, by favoring the appearance of diatom-diazotroph | | |
| symbiotic consortia. While during S1b and S2, a temporal coupling | | |
| between anammox and N2-fixation was not observed, either because loss | | |
| of bioavailable N was not sufficiently extensive or diazotrophs were | | |
| nutrient limited. During these periods, anammox may have acted as a | | |
| negative feedback on anoxia by quenching primary production.", | | |
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| "tags": [ | | "tags": [ |
| { | | { |
| "display_name": "Marine nitrogen cycle Sapropel Eastern | | "display_name": "Marine nitrogen cycle Sapropel Eastern |
| Mediterranean Sea Lipid biomarkers Anoxic events", | | Mediterranean Sea Lipid biomarkers Anoxic events", |
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| "name": "Marine nitrogen cycle Sapropel Eastern Mediterranean | | "name": "Marine nitrogen cycle Sapropel Eastern Mediterranean |
| Sea Lipid biomarkers Anoxic events", | | Sea Lipid biomarkers Anoxic events", |
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| n | "title": "Nitrogen cycling dynamics under altering redox conditions | n | "title": "Assessing marine nitrogen cycling dynamics under altering |
| during sapropels S1 and the ambiguous S2 in the Eastern Mediterranean | | redox conditions using depositions of sapropels S1 and the ambiguous |
| Sea", | | S2 in the Eastern Mediterranean Sea", |
| "type": "dataset", | | "type": "dataset", |
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| t | "version": "1" | t | "version": "2" |
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