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The first compilations of Proterozoic eukaryote diversity, published in the 1980s showed a dramatic peak in the Tonian Period (1000–720 Ma), interpreted as the initial radiation of eukaryotes in the marine realm. Over the decades, new discoveries filled in the older part of the record and the peak diminished, but the idea of a Tonian radiation of eukaryotes has remained strong, and is now widely accepted as fact. We present a new diversity compilation based on 181 species and 713 species occurrences from 145 formations ranging in age from 1890 Ma to 720 Ma and find a significant increase in diversity in the Tonian. However, we also find that the number of eukaryotic species through time is highly correlated with the number of formations in our dataset (i.e. eukaryote-bearing formations) through time. This correlation is robust to interpretations of eukaryote affinity, bin size, and bin boundaries. We also find that within-assemblage diversity—a measure thought to circumvent sampling bias—is related to the number of eukaryote-bearing formations through time. Biomarkers show a similar pattern to body fossils, where the rise of eukaryotic biosignatures correlates with increased sampling. We find no evidence that the proportion of eukaryote-bearing versus all fossiliferous formations changed through the Proterozoic, as might be expected if the correlation reflected an increase in eukaryote diversity driving an increase in the number of eukaryote-bearing formations. Although the correlation could reflect a common cause such as changes in sea level driving both diversification and an increase in sedimentary rock volume, we favor the explanation that the pattern of early eukaryote diversity is driven by variations in paleontological sampling. 

The upper Tonian ChUMP (Chuar-Uinta Mountains-Pahrump) strata of the southwestern U.S.A. are hypothesized to be regional correlatives and to record a time of rift basin evolution commencing at ca. 770 Ma in western Laurentia (modern-day coordinates). We test this correlation using U-Pb chemical abrasion-isotope dilution-thermal ionization mass spectrometry (CA-ID-TIMS) on detrital zircon grains from basal units within these successions. ChUMP units yield CA-ID-TIMS maximum depositional ages (MDA) between 775 and 766 Ma: the Chuar Group of AZ has an MDA of 770.1 ± 0.5 Ma (n = 1) and an additional young zircon mode at 775.7 ± 0.3 Ma (n = 11); the Uinta Mountain Group of northern UT has an MDA of 766.3 ± 0.5 Ma (n = 5) and contains a second young mode at 775.1 ± 0.7 Ma (n = 3); and the basal Horse Thief Springs Formation of the middle Pahrump Group CA has an MDA of 775.4 ± 0.7 Ma (n = 3). The ca. 775 and 770 Ma grains are interpreted to be from zircon-bearing mafic sources related to the 770–778 Ma Gunbarrel Large Igneous Province of Yukon and NW U.S.A. The 766 Ma population was either derived from the Mt Rogers complex of eastern Laurentia or could have come from conjugate margins that were in the process of rifting away, such as Tasmania. The CA-ID-TIMS dates on the Chuar Group in Grand Canyon anchor a Bayesian age model for evaluating late Tonian Earth systems. Faster sediment accumulation rates (80 + 150/-44 m/My) in the lower Chuar Group are consistent with the inception of an extensional basin related to Rodinia breakup; slower rates in the upper Chuar Group (25 + 12/-5 m/My) record are associated with relatively deeper water sedimentation and concomitant organic carbon burial during marine transgression. The model also constrains the timing of several biological events recorded in the Chuar Group, including eukaryovorous predation (>767 Ma), the first appearance of vase-shaped microfossils (∼741 Ma), and the ranges of Cerebrosphaera globosa (=C. buickii; 800–743 Ma) and Lanulatisphaera laufeldii. (766–740 Ma), both proposed as possible marine index fossils for late Tonian time. Finally, the model can also be used to search for stratigraphic evidence of a purported glaciation at ca. 751 Ma. 

Vase-shaped microfossils (VSMs) are found globally in middle Neoproterozoic (800–730 Ma) marine strata and represent the earliest evidence for testate (shell-forming) amoebozoans. VSM tests are hypothesized to have been originally organic in life but are most commonly preserved as secondary mineralized casts and molds. A few reports, however, suggest possible organic preservation. Here, we test the hypothesis that VSMs from shales of the lower Walcott Member of the Chuar Group, Grand Canyon, Arizona, contain original organic material, as reported by B. Bloeser in her pioneering studies of Chuar VSMs. We identified VSMs from two thin section samples of Walcott Member black shales in transmitted light microscopy and used scanning electron microscopy to image VSMs. Carbonaceous material is found within the internal cavity of all VSM tests from both samples and is interpreted as bitumen mobilized from Walcott shales likely during the Cretaceous. Energy dispersive X-ray spectroscopy (EDS) and wavelength dispersive X-ray spectroscopy (WDS) reveal that VSM test walls contain mostly carbon, iron, and sulfur, while silica is present only in the surrounding matrix. Raman spectroscopy was used to compare the thermal maturity of carbonaceous material within the samples and indicated the presence of pyrite and jarosite within fossil material. X-ray absorption spectroscopy revealed the presence of reduced organic sulfur species within the carbonaceous test walls, the carbonaceous material found within test cavities, and in the sedimentary matrix, suggesting that organic matter sulfurization occurred within the Walcott shales. Our suite of spectroscopic analyses reveals that Walcott VSM test walls are organic and sometimes secondarily pyritized (with the pyrite variably oxidized to jarosite). Both preservation modes can occur at a millimeter spatial scale within sample material, and at times even within a single specimen. We propose that sulfurization within the Walcott Shales promoted organic preservation, and furthermore, the ratio of iron to labile VSM organic material controlled the extent of pyrite replacement. Based on our evidence, we conclude that the VSMs are preserved with original organic test material, and speculate that organic VSMs may often go unrecognized, given their light-colored, translucent appearance in transmitted light.