Phosphatic scales in vase‐shaped microfossil assemblages from Death Valley, Grand Canyon, Tasmania, and Svalbard

Abstract Although biomineralized skeletal elements dominate the Phanerozoic fossil record, they did not become common until ~550–520 Ma when independent acquisitions of biomineralization appeared in multiple lineages of animals and a few protists (single‐celled eukaryotes). Evidence of biomineraliza...

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Bibliographic Details
Published in:Geobiology
Main Authors: Riedman, Leigh Anne, Porter, Susannah M., Czaja, Andrew D.
Other Authors: Cushman Foundation for Foraminiferal Research, NASA Astrobiology Institute, Palaeontological Association, University of Cincinnati, National Science Foundation
Format: Article in Journal/Newspaper
Language:English
Published: Wiley 2021
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Online Access:http://dx.doi.org/10.1111/gbi.12439
https://onlinelibrary.wiley.com/doi/pdf/10.1111/gbi.12439
https://onlinelibrary.wiley.com/doi/full-xml/10.1111/gbi.12439
https://onlinelibrary.wiley.com/doi/am-pdf/10.1111/gbi.12439
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Summary:Abstract Although biomineralized skeletal elements dominate the Phanerozoic fossil record, they did not become common until ~550–520 Ma when independent acquisitions of biomineralization appeared in multiple lineages of animals and a few protists (single‐celled eukaryotes). Evidence of biomineralization preceding the late Ediacaran is spotty aside from the apatitic scale microfossils of the ~811 Ma Fifteenmile Group, northwestern Canada. Here, we describe scale‐shaped microfossils from four vase‐shaped microfossil (VSM)‐bearing units of later Tonian age: the Togari Group of Tasmania, Chuar and Pahrump groups of southwestern United States, and the Roaldtoppen Group of Svalbard. These scale‐shaped microfossils consist of thin, ~13 micron‐long plates typically surrounded by a 1–3 micron‐thick colorless envelope; they are found singly and in heterotypic and monotypic clusters of a few to >20 specimens. Raman spectroscopy and confocal laser scanning microscopy indicate these microfossils are composed of apatite and kerogen, just as is seen in the Fifteenmile Group scale microfossils. Despite compositional similarity, however, these scales are probably not homologous, representing instead, an independent acquisition of apatite mineralization. We propose that these apatite‐kerogen scale‐shaped microfossils are skeletal elements of a protistan cell. In particular, their consistent co‐occurrence with VSMs, and similarities with scales of arcellinid testate amoebae, a group to which the VSMs are thought to belong, suggest the possibility that these microfossils may be test‐forming scales of ancient arcellinid testate amoebae. The apparent apatite biomineralization in both these microfossils and the Fifteenmile scales is unexpected given its exceedingly rare use in skeletons of modern protists. This modern absence is attributed to the extravagance of using a limiting nutrient in a structural element, but multiple occurrences of apatite biomineralization in the Tonian suggest that phosphorus was not a limiting nutrient ...