GLORIA

GEOMAR Library Ocean Research Information Access

feed icon rss

Your email was sent successfully. Check your inbox.

An error occurred while sending the email. Please try again.

Proceed reservation?

Export
Filter
  • ACS (American Chemical Society)  (1)
  • Amsterdam [u.a.] : Elsevier  (1)
  • Geological Society of America, GSA  (1)
  • 1
    Book
    Book
    Amsterdam [u.a.] : Elsevier
    Type of Medium: Book
    Pages: VI, 194 S , Ill., graph. Darst
    Series Statement: Marine chemistry 120.2010,1/4
    Language: English
    Location Call Number Limitation Availability
    BibTip Others were also interested in ...
  • 2
    Publication Date: 2021-02-08
    Description: A negative shift in the calcium isotopic composition of marine carbonate rocks spanning the end-Permian extinction horizon in South China has been used to argue for an ocean acidification event coincident with mass extinction. This interpretation has proven controversial, both because the excursion has not been demonstrated across multiple, widely separated localities, and because modeling results of coupled carbon and calcium isotope records illustrate that calcium cycle imbalances alone cannot account for the full magnitude of the isotope excursion. Here, we further test potential controls on the Permian-Triassic calcium isotope record by measuring calcium isotope ratios from shallow-marine carbonate successions spanning the Permian-Triassic boundary in Turkey, Italy, and Oman. All measured sections display negative shifts in δ44/40Ca of up to 0.6‰. Consistency in the direction, magnitude, and timing of the calcium isotope excursion across these widely separated localities implies a primary and global δ44/40Ca signature. Based on the results of a coupled box model of the geological carbon and calcium cycles, we interpret the excursion to reflect a series of consequences arising from volcanic CO2 release, including a temporary decrease in seawater δ44/40Ca due to short-lived ocean acidification and a more protracted increase in calcium isotope fractionation associated with a shift toward more primary aragonite in the sediment and, potentially, subsequently elevated carbonate saturation states caused by the persistence of elevated CO2 delivery from volcanism. Locally, changing balances between aragonite and calcite production are sufficient to account for the calcium isotope excursions, but this effect alone does not explain the globally observed negative excursion in the δ13C values of carbonate sediments and organic matter as well. Only a carbon release event and related geochemical consequences are consistent both with calcium and carbon isotope data. The carbon release scenario can also account for oxygen isotope evidence for dramatic and protracted global warming as well as paleontological evidence for the preferential extinction of marine animals most susceptible to acidification, warming, and anoxia.
    Type: Article , PeerReviewed
    Format: text
    Location Call Number Limitation Availability
    BibTip Others were also interested in ...
  • 3
    Publication Date: 2022-01-31
    Description: Lead concentrations [Pb] and isotope ratios (Pb-206/Pb-207, Pb-208/Pb-207) have been measured in samples of total suspended particulate (TSP) aerosols, seawater, and suspended and sinking particles in the Gulf of Aqaba (GOA), Red Sea. Isotope ratios of Pb in seawater and in the soluble fraction of Pb in atmospheric TSP were similar suggesting that TSP is an important source of Pb in this area. Pb concentrations in seawater measured in this study (max 76.8 pmol kg(-1)) were much lower than those recorded at the same location in 2003-2004 (up to 1000 pmol kg(-1)). Changes in Pb isotope ratios in TSP depositions in these years indicate that leaded gasoline was responsible for the high dissolved Pb in GOA more than a decade ago and that recent regulation reduced Pb contamination. The similarity in Pb isotope ratios in suspended and sinking particles implies close interactions between these two size fractions. This study demonstrates the effect of the phasing out of leaded gasoline on TSP and seawater Pb chemistry in the Northern GOA; the rate of change in dissolved Pb concentrations in the GOA is faster than that reported for the open ocean possibly due to higher particle scavenging and the relatively short residence time of deep water in the Basin.
    Type: Article , PeerReviewed
    Format: text
    Format: text
    Location Call Number Limitation Availability
    BibTip Others were also interested in ...
Close ⊗
This website uses cookies and the analysis tool Matomo. More information can be found here...