Oxygen isotope analysis of biogenic phosphate: An application to the Early Eocene Thermal Maximum
The
principal method used to determine the stable oxygen isotopic composition of
biogenic phosphate (δ18Obp)
is by precipitation and analysis of silver phosphate (Ag3PO4). Procedural improvements over time have
focused on replacing HNO3 with HF as the dissociation agent, and
dilution of the HPO4+ -containing supernatant prior to
precipitation of Ag3PO4, in both cases providing more
precise data. However, since the inception of this procedure, the amount of
biogenic phosphate used as starting sample has been in the range of five to
hundreds of milligrams. My development research shows that using greatly
reduced sample sizes (one to six milligrams of starting material) results in
comparable precision to previous techniques. This change in procedure provides
new opportunity for δ18Obp analysis, where biogenic
phosphate samples previously considered too small or too prized can now be
analyzed.
Samples
for isotopic analysis in this study include large herbivorous mammals and gar
from the Eocene of North America. Tapiromorph tooth enamel samples from
a high-latitude site, and Coryphodon and gar scales from separate
mid-latitude sites have been analyzed with these new, smaller starting sample
sizes. Specimens come from strata of Wasatchian age (NALMA), correlating to the
Early Eocene Thermal Maximum (EETM). This time is hypothesized to have been,
globally, one of the warmest periods in the last 65 my. Data reported here show
Mean Annual Temperature (MAT) estimates for mid-latitudes to range from ~18 to
19°C, and a MAT high-latitude estimate of ~4.5°C from continental