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Abstract Competing hypotheses attribute the regional loss of 1.2–1.0 Ga detrital zircon from the Cambrian Sauk Sequence in southwestern North America to differing tectonic controls on surface topography. We test three hypotheses with source‐to‐sink detrital zircon provenance analysis via tandem in situ and isotope dilution U–Pb geochronology paired with geochemical and Hf‐isotope tracers. Our data indicate that the lower‐to‐middle Sixtymile Formation in Grand Canyon was derived from ca. 1.1 Ga rocks of the Llano Uplift and the ca. 539–523 Ma Wichita igneous province, approximately 1400 km away. In contrast, new U–Pb geochronology links the upper Sixtymile and Tapeats formations to the 513–510 Ma Florida Mountains intrusive complex, southern New Mexico, and proximal 1.4 and 1.7 Ga basement approximately 650 km away. We attribute a regional provenance shift to plume–lithosphere interactions on the Iapetan margin, tectonism along ‘leaky’ intracratonic transverse fault zones and the rift‐to‐drift transition on the Cordilleran margin. 

Abstract High-precision U-Pb zircon ages on SE Newfoundland tuffs now bracket the Avalonian Lower–Middle Cambrian boundary. Upper Lower Cambrian Brigus Formation tuffs yield depositional ages of 507.91 ± 0.07 Ma (Callavia broeggeriZone) and 507.67 ± 0.08 Ma and 507.21 ± 0.13 Ma (Morocconus-Condylopyge eliAssemblage interval). Lower Middle Cambrian Chamberlain’s Brook Formation tuffs have depositional ages of 506.34 ± 0.21 Ma (Kiskinella cristataZone) and 506.25 ± 0.07 Ma (Eccaparadoxides bennettiZone). The composite unconformity separating the Brigus and Chamberlain’s Brook formations is constrained between these ages. An Avalonian Lower–Middle Cambrian boundary between 507.2 ± 0.1 and 506.3 ± 0.2 Ma is consistent with maximum depositional age constraints from southwest Laurentia, which indicate an age for the base of the Miaolingian Series, as locally interpreted, of ≤ 506.6 ± 0.3 Ma. The Miaolingian Series’ base is interpreted as correlative within ≤ 0.3 ± 0.3 Ma between Cambrian palaeocontinents, although its exact synchrony is questionable due to taxonomic problems with a possibleOryctocephalus indicus-plexus, invariable dysoxic lithofacies control ofO. indicusand diachronous occurrence ofO. indicusin temporally distinct δ¹³C chemozones in South China and SW Laurentia. The lowest occurrence ofO. indicusassemblages is linked to onlap (epeirogenic or eustatic) of dysoxic facies. A united Avalonia is shown by late Early Cambrian volcanics in SW New Brunswick; Cape Breton Island; SE Newfoundland; and the Wrekin area, England. The new U-Pb ages revise Avalonian geological evolution as they show rapid epeirogenic changes through depositional sequences 4a–6. 

The Cambrian Tonto Group of the Grand Canyon was used by Edwin McKee in 1945 to make an insightful visual representation of how sedimentary facies record transgression across a craton—a common conceptual framework still used in geologic education. Although the tenets of McKee’s facies diagram persist, the integration of new stratigraphy, depositional models, paleontology, biostratigraphy, and other data is refining the underlying dynamics of this cratonic transgression. Instead of McKee’s interpretation of one major transgression with only minor regressions, there are at least five stratigraphic sequences, of which the lower three are separated by disconformities. These hiatal surfaces likely represent erosion of previously deposited Cambrian sediments that were laid down on the tropical, pre-vegetated landscape. Rather than being fully marine in origin, these sequences were formed by a mosaic of depositional environments including braided coastal plain, eolian, marginal marine, and various shallow marine environments. McKee, not having the insights of sequence stratigraphy and plate tectonics, concluded that the preservation of these sediments were due to predepositional topography and subsidence of the “geosyncline.” Our modern interpretation is that accommodation space was a result of eustasy and differential subsidence on the continental margin. Our modified depositional model provides a more effective teaching tool for fundamentals and nuances of modern stratigraphic thinking, using the Tonto Group as a still-influential type location for understanding transgressive successions. 

Abstract The Steptoean Positive Isotopic Carbon Excursion (SPICE) is a prominent +4–5‰ shift in the Cambrian δ13C record used for global chronostratigraphic correlation. The onset of this excursion is traditionally placed at the base of the Pterocephaliid trilobite biomere (base of the Furongian Series). Recent studies have documented local controls on the expression of the SPICE and emphasize the need for chronostratigraphic standards for these complex biogeochemical signals. We build upon prior work in western Laurentia by integrating δ13C and biostratigraphy with high-precision isotope dilution U-Pb detrital zircon maximum depositional ages that are coincident with the onset, peak, and falling limb of the SPICE. Our study provides the first useful numerical age constraint for the onset of the SPICE and the Laurentian trilobite biozones and requires revision of the late Cambrian geologic time scale boundaries by several million years. 

Abstract We applied tandem U-Pb dating of detrital zircon (DZ) to redefine the Tonto Group in the Grand Canyon region (Arizona, USA) and to modify the Cambrian time scale. Maximum depositional ages (MDAs) based upon youngest isotope-dilution DZ ages for the Tapeats Sandstone are ≤508.19 ± 0.39 Ma in eastern Grand Canyon, ≤507.68 ± 0.36 Ma in Nevada, and ≤506.64 ± 0.32 Ma in central Arizona. The Sixtymile Formation, locally conformable below the Tapeats Sandstone, has a similar MDA (≤508.6 ± 0.8 Ma) and is here added to the Tonto Group. We combined these precise MDAs with biostratigraphy of trilobite biozones in the Tonto Group. The Tapeats Sandstone is ca. 508–507 Ma; the Bright Angel Formation contains Olenellus, Glossopleura, and Ehmaniella biozones and is ca. 507–502 Ma; and the Muav Formation contains Bolaspidella and Cedaria biozones and is ca. 502–499 Ma. The Frenchman Mountain Dolostone is conformable above the Muav Formation and part of the same transgression; it replaces McKee’s Undifferentiated Dolomite as part of the Tonto Group; it contains the Crepicephalus Biozone and is 498–497 Ma. The Tonto Group thickens east to west, from 250 m to 830 m, due to ∼300 m of westward thickening of carbonates plus ∼300 m of eastward beveling beneath the sub-Devonian disconformity. The trilobite genus Olenellus occurs in western but not eastern Grand Canyon; it has its last appearance datum (LAD) in the Bright Angel Formation ∼45 m above the ≤507.68 Ma horizon. This extinction event is estimated to be ca. 506.5 Ma and is two biozones below the Series 2–Miaolingian Epoch boundary, which we estimate to be ca. 506 Ma. Continued tandem dating of detrital grains in stratigraphic context, combined with trilobite biostratigraphy, offers rich potential to recalibrate the tempo and dynamics of Cambrian Earth systems. 

Abstract Trilobites appeared and diversified rapidly in the Cambrian, but it is debated as to whether their radiations and extinctions were globally synchronous or geographically restricted and diachronous. The end of the early Cambrian is a classic example—it has traditionally been defined by the extinction of olenellid and redlichiid trilobites and the appearance of paradoxidid trilobites. Here we integrate the global biostratigraphy of these three trilobite groups with high-precision tuff and tandem detrital zircon U-Pb age constraints to falsify prior models for global synchronicity of these events. For the first time, we demonstrate that olenellid trilobites in Laurentia went extinct at least 3 Ma after the first appearance of paradoxidids in Avalonia and West Gondwana (ca. 509 Ma). They also disappeared before the extinction of redlichiids and prior to the base of the Miaolingian at ca. 506 Ma in South China. This indicates that these three trilobite groups (paradoxidids, olenellids, and redlichiids) and their associated biotas overlapped in time for nearly 40% of Cambrian Epoch 2, Age 4. Implications of this chronological overlap are: (1) trilobite transitions were progressive and geographically mediated rather than globally synchronous; and (2) paleontological databases underestimate the diversity of the early Cambrian. This ∼3 Ma diachroneity, at a critical time in the early evolution of animals, also impacts chemostratigraphic and paleoclimatic data sets that are tied to trilobite biostratigraphy and that collectively underpin our understanding of the Cambrian Earth system.