@article{526c3a92f3314f0b9f5c39d32effe2f1,
title = "Degradation of Internal Organic Matter is the Main Control on Pteropod Shell Dissolution After Death",
abstract = "The potential for preservation of thecosome pteropods is thought to be largely governed by the chemical stability of their delicate aragonitic shells in seawater. However, sediment trap studies have found that significant carbonate dissolution can occur above the carbonate saturation horizon. Here we present the results from experiments conducted on two cruises to the Scotia Sea to directly test whether the breakdown of the organic pteropod body influences shell dissolution. We find that on the timescales of 3 to 13 days, the oxidation of organic matter within the shells of dead pteropods is a stronger driver of shell dissolution than the aragonite saturation state of seawater. Three to four days after death, shells became milky white and nano scanning electron microscope images reveal smoothing of internal surface features and increased shell porosity, both indicative of aragonite dissolution. These findings have implications for the interpretation of the condition of pteropod shells from sediment traps and the fossil record, as well as for understanding the processes controlling particulate carbonate export from the surface ocean.",
author = "Oakes, {R. L.} and Peck, {V. L.} and C. Manno and Bralower, {T. J.}",
note = "Funding Information: The authors declare no conflicts of interest. The data presented in the figures are available in the supporting information. The reconstructed CT data are available on Dryad doi:10.5061/dryad.8ts30t5. This work was carried out as part of the Ecosystems programme at the British Antarctic Survey. The authors would like to thank the crew and scientists of cruises JR271 and JR15002 for making the sample collection and decay experiments possible. Thanks to J. Urbanski, W. Yetter, and the team at GE in Lewistown, PA, for help with CT scanning and to J. Anderson and W. Auker from the MCL lab at Penn State for help with the SEM. Thanks to M. Humphreys for help with carbonate chemistry calculations, J. Gardner for the carbonate chemistry measurement for the 3.5-day decay experiment, and S. Sandrini for help with carbonate chemistry analysis for the 13-day decay experiment. The authors thank one anonymous reviewer whose comments helped to improve the quality of the manuscript. R. L. O. received funding from the Ellis L. Yochelson Award, the Hiroshi and Koya Ohmoto Graduate Student Fellowship, and the Alley Family Graduate Scholarship to support this work. R. L. O. and T. J. B. received funding from the Deike Research Fellowship. Publisher Copyright: {\textcopyright}2019. American Geophysical Union. All Rights Reserved.",
year = "2019",
month = jun,
doi = "10.1029/2019GB006223",
language = "English (US)",
volume = "33",
pages = "749--760",
journal = "Global Biogeochemical Cycles",
issn = "0886-6236",
publisher = "American Geophysical Union",
number = "6",
}