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  • 1
    In: Revue de Micropaléontologie, Elsevier BV, Vol. 61, No. 3-4 ( 2018-12), p. 113-138
    Type of Medium: Online Resource
    ISSN: 0035-1598
    RVK:
    Language: English
    Publisher: Elsevier BV
    Publication Date: 2018
    detail.hit.zdb_id: 2138980-9
    SSG: 13
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  • 2
    Online Resource
    Online Resource
    Wiley ; 2021
    In:  Rapid Communications in Mass Spectrometry Vol. 35, No. 8 ( 2021-04-30)
    In: Rapid Communications in Mass Spectrometry, Wiley, Vol. 35, No. 8 ( 2021-04-30)
    Abstract: Since their introduction more than a decade ago, isotope ratio infrared spectroscopy (IRIS) systems have rapidly become the standard for oxygen ( δ 18 O) and hydrogen ( δ 2 H) isotope analysis of water samples. An important disadvantage of IRIS systems is the well‐documented sample‐to‐sample memory effect, which requires each sample to be analyzed multiple times before the desired accuracy is reached, lengthening analysis times and driving up the costs of analyses. Methods We present an adapted set‐up and calculation protocol for fully automated analysis of water samples using a Picarro L2140‐i cavity ring‐down spectroscopy instrument. The adaptation removes memory effects by use of a continuously moisturized nitrogen carrier gas. Water samples of 0.5 μL are measured on top of the water vapor background, after which isotope ratios are calculated by subtraction of the background from the sample peaks. Results With this new technique, single injections of water samples have internal precisions (1 σ ) below 0.05‰ for δ 18 O values and 0.1‰ for δ 2 H values, regardless of the isotope ratio of the previous sample. Precision is worse, however, when the isotope difference between the sample and background water is too large (i.e., exceeding approximately 9‰ for δ 18 O values and 70‰ for δ 2 H values). Isotope ratios show negligible drift across the four weeks within which the experiments were performed. The single‐injection 1 σ precision for 17 O excess (Δ′ 17 O) determined with this method is 60 per meg. Conclusions Our experiments demonstrate that by removing sample‐to‐sample memory effects with a moisturized carrier gas, the time for measurement of δ 18 O and δ 2 H values using an IRIS system can be reduced markedly without compromising the analytical precision and accuracy. Thorough replication is needed to achieve sufficiently low uncertainties for Δ′ 17 O.
    Type of Medium: Online Resource
    ISSN: 0951-4198 , 1097-0231
    URL: Issue
    Language: English
    Publisher: Wiley
    Publication Date: 2021
    detail.hit.zdb_id: 2002158-6
    detail.hit.zdb_id: 58731-X
    SSG: 11
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  • 3
    In: Global Change Biology, Wiley, Vol. 26, No. 3 ( 2020-03), p. 1338-1353
    Abstract: Historical coral skeleton (CS) δ 18 O and δ 15 N records were produced from samples recovered from sedimentary deposits, held in natural history museum collections, and cored into modern coral heads. These records were used to assess the influence of global warming and regional eutrophication, respectively, on the decline of coastal coral communities following the development of the Pearl River Delta (PRD) megacity, China. We find that, until 2007, ocean warming was not a major threat to coral communities in the Pearl River estuary; instead, nitrogen (N) inputs dominated impacts. The high but stable CS‐δ 15 N values (9‰–12‰ vs. air) observed from the mid‐Holocene until 1980 indicate that soil and stream denitrification reduced and modulated the hydrologic inputs of N, blunting the rise in coastal N sources during the early phase of the Pearl River estuary urbanization. However, an unprecedented CS‐δ 15 N peak was observed from 1987 to 1993 ( 〉 13‰ vs. air), concomitant to an increase of NH 4 + concentration, consistent with the rapid Pearl River estuary urbanization as the main cause for this eutrophication event. We suggest that widespread discharge of domestic sewage entered directly into the estuary, preventing removal by natural denitrification hotspots. We argue that this event caused the dramatic decline of the Pearl River estuary coral communities reported from 1980 to 2000. Subsequently, the coral record shows that the implementation of improved wastewater management policies succeeded in bringing down both CS‐δ 15 N and NH 4 + concentrations in the early 2000s. This study points to the potential importance of eutrophication over ocean warming in coral decline along urbanized coastlines and in particular in the vicinity of megacities.
    Type of Medium: Online Resource
    ISSN: 1354-1013 , 1365-2486
    URL: Issue
    Language: English
    Publisher: Wiley
    Publication Date: 2020
    detail.hit.zdb_id: 2020313-5
    SSG: 12
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  • 4
    In: Rapid Communications in Mass Spectrometry, Wiley, Vol. 34, No. 16 ( 2020-08-30)
    Abstract: Online oxygen ( δ 18 O) and hydrogen ( δ 2 H) isotope analysis of fluid inclusion water entrapped in minerals is widely applied in paleo‐fluid studies. In the state of the art of fluid inclusion isotope research, however, there is a scarcity of reported inter‐technique comparisons to account for possible analytical offsets. Along with improving analytical precisions and sample size limitations, interlaboratory comparisons can lead to a more robust application of fluid inclusion isotope records. Methods Mineral samples—including speleothem, travertine, and vein material—were analyzed on two newly setup systems for fluid inclusion isotope analysis to provide an inter‐platform comparison. One setup uses a crusher unit connected online to a continuous‐flow pyrolysis furnace and an isotope ratio mass spectrometry (IRMS) instrument. In the other setup, a crusher unit is lined up with a cavity ring‐down spectroscopy (CRDS) system, and water samples are analyzed on a continuous standard water background to achieve precisions on water injections better than 0.1‰ for δ 18 O values and 0.4‰ for δ 2 H values for amounts down to 0.2 μL. Results Fluid inclusion isotope analyses on the IRMS setup have an average 1 σ reproducibility of 0.4‰ and 2.0‰ for δ 18 O and δ 2 H values, respectively. The CRDS setup has a better 1 σ reproducibility (0.3‰ for δ 18 O values and 1.1‰ for δ 2 H values) and also a more rapid sample throughput ( 〈 30 min per sample). Fluid inclusion isotope analyses are reproducible at these uncertainties for water amounts down to 0.1 μL on both setups. Fluid inclusion isotope data show no systematic offsets between the setups. Conclusions The close match in fluid inclusion isotope results between the two setups demonstrates the high accuracy of the presented continuous‐flow techniques for fluid inclusion isotope analysis. Ideally, experiments such as the one presented in this study will lead to further interlaboratory comparison efforts and the selection of suitable reference materials for fluid inclusion isotopes studies.
    Type of Medium: Online Resource
    ISSN: 0951-4198 , 1097-0231
    URL: Issue
    Language: English
    Publisher: Wiley
    Publication Date: 2020
    detail.hit.zdb_id: 2002158-6
    detail.hit.zdb_id: 58731-X
    SSG: 11
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  • 5
    In: Nature Communications, Springer Science and Business Media LLC, Vol. 14, No. 1 ( 2023-08-25)
    Abstract: There is limited understanding of temperature and atmospheric circulation changes that accompany an Atlantic Meridional Overturning Circulation (AMOC) slowdown beyond the North Atlantic realm. A Peqi’in Cave (Israel) speleothem dated to the last interglacial period (LIG), 129–116 thousand years ago (ka), together with a large modern rainfall monitoring dataset, serve as the base for investigating past AMOC slowdown effects on the Eastern Mediterranean. Here, we reconstruct LIG temperatures and rainfall source using organic proxies (TEX 86 ) and fluid inclusion water d-excess . The TEX 86 data show a stepwise cooling from 19.8 ± 0.2° ( ca . 128–126 ka) to 16.5 ± 0.6 °C ( ca . 124–123 ka), while d-excess values decrease abruptly ( ca . 126 ka). The d-excess shift suggests that rainfall was derived from more zonal Mediterranean air flow during the weakened AMOC interval. Decreasing rainfall d-excess trends over the last 25 years raise the question whether similar atmospheric circulation changes are also occurring today.
    Type of Medium: Online Resource
    ISSN: 2041-1723
    Language: English
    Publisher: Springer Science and Business Media LLC
    Publication Date: 2023
    detail.hit.zdb_id: 2553671-0
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  • 6
    In: Nature Geoscience, Springer Science and Business Media LLC, Vol. 14, No. 12 ( 2021-12), p. 937-941
    Abstract: During glacial terminations, massive iceberg discharges and meltwater pulses in the North Atlantic triggered a shutdown of the Atlantic Meridional Overturning Circulation (AMOC). Speleothem calcium carbonate oxygen isotope records (δ 18 O Cc ) indicate that the collapse of the AMOC caused dramatic changes in the distribution and variability of the East Asian and Indian monsoon rainfall. However, the mechanisms linking changes in the intensity of the AMOC and Asian monsoon δ 18 O Cc are not fully understood. Part of the challenge arises from the fact that speleothem δ 18 O Cc depends on not only the δ 18 O of precipitation but also temperature and kinetic isotope effects. Here we quantitatively deconvolve these parameters affecting δ 18 O Cc by applying three geochemical techniques in speleothems covering the penultimate glacial termination. Our data suggest that the weakening of the AMOC during meltwater pulse 2A caused substantial cooling in East Asia and a shortening of the summer monsoon season, whereas the collapse of the AMOC during meltwater pulse 2B (133,000 years ago) also caused a dramatic decrease in the intensity of the Indian summer monsoon. These results reveal that the different modes of the AMOC produced distinct impacts on the monsoon system.
    Type of Medium: Online Resource
    ISSN: 1752-0894 , 1752-0908
    Language: English
    Publisher: Springer Science and Business Media LLC
    Publication Date: 2021
    detail.hit.zdb_id: 2396648-8
    detail.hit.zdb_id: 2405323-5
    SSG: 16,13
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  • 7
    In: Rapid Communications in Mass Spectrometry, Wiley, Vol. 34, No. 19 ( 2020-10-15)
    Abstract: Oxygen (δ 18 O) and carbon (δ 13 C) isotope analysis of foraminifera and other CaCO 3 samples has been a key technique for paleoceanographical and paleoclimatological research for more than 60 years. There is ongoing demand for the analysis of ever smaller CaCO 3 samples, driven, for example, by the desire to analyse single specimen planktic foraminifera, or small samples of tooth enamel. Methods We present a continuous‐flow mass spectrometric technique that uses cryo‐focusing of sample CO 2 to analyse CaCO 3 samples in a weight range between 10 and 3 μg. These are considerably lower sample weights than achievable on most currently available standard instrumentation. The technique is automated, so that sample throughput lies at 〉 60 samples per day. The method involves an on‐line vial‐flushing routine designed to remove machine drift due to blank CO 2 build‐up in the sample vials. Results In a series of experiments the effect of blank CO 2 build‐up is quantified, and outgassing from the chlorobutyl septa identified as the source. An improved flushing routine together with the use of a cryo‐focusing step in the analysis is demonstrated to provide the analytical stability and sensitivity to analyse CaCO 3 samples in a weight range between 10 and 3 μg at ≤0.1‰ precision (1σ) for both δ 18 O and δ 13 C values. The technique yields similarly precise results for the analysis of the structural carbonate fraction of small tooth enamel samples. Conclusions This study demonstrates that high‐precision oxygen and carbon isotope analysis is possible on CaCO 3 samples smaller than 5 μg by use of a continuous‐flow isotope technique. Of key importance are (1) the application of a cold trap that drastically reduces sample gas loss, and (2) a modified flushing regime that eliminates increasing background CO 2 build‐up in sample vials during longer automated sample runs.
    Type of Medium: Online Resource
    ISSN: 0951-4198 , 1097-0231
    URL: Issue
    Language: English
    Publisher: Wiley
    Publication Date: 2020
    detail.hit.zdb_id: 2002158-6
    detail.hit.zdb_id: 58731-X
    SSG: 11
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