Paleogene time scale miscalibration: Evidence from the dating of the North Atlantic igneous province

Jolley et al. (2002) have proposed that the date of the Paleocene - Eocene thermal maximum is ca. 60 Ma, at least 5 m.y. older than currently estimated and, as a result, argue that the Paleogene time scale of Berggren et al. (1995) is grossly miscalibrated. The implications of this proposal are implausible, and we attribute the discrepancy in age noted by Jolley et al. (2002) to miscorrelation of the Staffa-type palynofloras and ambiguous isotopic dates from the North Atlantic igneous province

Pleistocene magnetochronology of early hominin sites at Ceprano and Fontana Ranuccio, Italy

Paleomagnetic analyses were conducted on two cores drilled at Ceprano in central Italy where an incomplete hominin cranium was discovered in 1994, as well as on two additional cores from the nearby site of Fontana Ranuccio that yielded hominin remains associated with an Acheulean industry. No evidence for the 0.78 Ma Brunhes–Matuyama boundary was found at Ceprano down to 45 m below the level that yielded the hominin cranium. The Ceprano lithostratigraphy and the paleomagnetic age constraints are broadly consistent with the stratigraphy of the Liri lacustrine sequence of the Latina Valley, constrained by published K–Ar ages between ~ 0.6 and ~ 0.35 Ma, and according to an age model with magnetic susceptibility supported by pollen facies data, suggest that the level that yielded the hominin cranium has an age of ~ 0.45 (+ 0.05, − 0.10) Ma. Evidence for the Brunhes–Matuyama boundary was found at Fontana Ranuccio about 40 m below the hominin level, consistent with a K–Ar age of ~ 0.46 Ma reported for this level. Hence the Ceprano and Fontana Ranuccio hominin occurrences may be of very similar mid-Brunhes age

Pleistocene magnetochronology of early hominin sites at Ceprano and Fontana Ranuccio, Italy

Paleomagnetic analyses were conducted on two cores drilled at Ceprano in central Italy where an incomplete hominin cranium was discovered in 1994, as well as on two additional cores from the nearby site of Fontana Ranuccio that yielded hominin remains associated with an Acheulean industry. No evidence for the 0.78 Ma Brunhes–Matuyama boundary was found at Ceprano down to 45 m below the level that yielded the hominin cranium. The Ceprano lithostratigraphy and the paleomagnetic age constraints are broadly consistent with the stratigraphy of the Liri lacustrine sequence of the Latina Valley, constrained by published K–Ar ages between ~ 0.6 and ~ 0.35 Ma, and according to an age model with magnetic susceptibility supported by pollen facies data, suggest that the level that yielded the hominin cranium has an age of ~ 0.45 (+ 0.05, − 0.10) Ma. Evidence for the Brunhes–Matuyama boundary was found at Fontana Ranuccio about 40 m below the hominin level, consistent with a K–Ar age of ~ 0.46 Ma reported for this level. Hence the Ceprano and Fontana Ranuccio hominin occurrences may be of very similar mid-Brunhes age

The Geology of Ukhaa Tolgod (Djadokhta Formation, Upper Cretaceous, Nemegt Basin, Mongolia)

The lithostratigrahy and sedimentology of the fossiliferous Upper Cretaceous strata exposed in the Gobi Desert of Mongolia at Ukhaa Tolgod are described and mapped on aerial photos. Topographic features are also mapped by plane table and alidade. Five lithologic and sedimentologic facies are described: E-1, distinctly cross-stratified sandstone with fine structure, interpreted to represent eolian dune deposits; E-2, vaguely bedded sandstone with cross-stratified concretionary sheets, interpreted to represent eolian dune deposits modified by diagenetic formation of slope-parallel concretionary sheets of pedogenic calcite; S, structureless sandstone lacking concretions or cross-strata, interpreted to represent sandslide deposits generated by mass wasting along the lee slopes; C, conglomerate interpreted to represent basin-margin conglomerates washed into the dune field from adjacent topographic highs; and M, mudstone and siltstone interpreted to represent interdune deposition in ephemeral ponds and lakes. Facies E-2 and S have not been reported previously. Eleven stratigraphic sections at various localities within the Ukhaa Tolgod drainage basin are documented. The exposed composite section consists of about 75 m of pale orange sandstones, greenish-brown conglomerates, and brown siltstones that are products of an arid environment. Four schematic cross sections are documented to illustrate the lateral relationships among the five facies. In the Ukhaa Tolgod area, the beds dip about 2.5u to the south, away from the nearby Gilbent Range. This structural attitude is interpreted to be related to the uplift of the Gilbent block along normal faults exposed at the base of the range. The dune-derived sandslides of Facies S contain a rich skeletal fauna of Late Cretaceous dinosaurs, mammals, and lizards. Essentially, all the skeletal remains collected at Ukhaa Tolgod come from Facies S. Facies E-1 does contain numerous, concave-up depressions in the cross-strata interpreted as vertebrate tracks. Facies E-2 contains abundant cylindrical structures interpreted as burrows. The strata at Ukhaa Tolgod are referred to the Djadokhta Formation. As seen in the Bayn Dzak Member at Bayn Dzak, facies E-1, E-2, S, and M dominate the lower part of the section at Ukhaa Tolgod, with prominent beds of Facies C exposed near the top. Accordingly, the exposures at Ukhaa Tolgod are referred to the Bayn Dzak Member of the Djadokhta Formation. Classic exposures of the Barun Goyot Formation at Khulsan differ in having units of flat-bedded sandstone intercalated with beds of Facies S near the top of the section. To date, over 1,000 vertebrate skulls and skeletons have been collected from Facies S. Most are preserved as float contained in small calcareous nodules; however, some were found in situ. Many specimens represent either fairly complete skulls or skulls with articulated or associated postcranial skeletons. Based on faunal similarities between Bayn Dzak and Ukhaa Tolgod, the fauna at Ukhaa Tolgod is interpreted to reflect a Campanian age. The rich assemblage of fossils makes Ukhaa Tolgod one of the richest Late Cretaceous vertebrate fossil localities in the world, and the fossils provide unique insights into evolutionary developments of mammals, lizards, and dinosaurs, including birds, less than 10 my before the terminal Cretaceous extinction event

Toward a Revised Paleogene Geochronology

New information has become available that requires a revision of Paleogene chronology incorporated in most current Cenozoic time scales. Age estimates for the limits of the Paleogene (the Oligocene/Miocene and Cretaceous/Paleogene boundaries) have not changed appreciably and remain at about 24 Ma and about 66 Ma, respectively. However, new radioisotope data indicate that boundaries of subdivisions within the Paleogene are generally younger than previously estimated, for example, the Paleocene/Eocene and Eocene/Oligocene, by about 2 to 3 m.y. We review the current status of magnetobiostratigraphic correlations and new radioisotope data, with particular reference to late Eocene~early Oligocene geochronology and provide a reassessment of the age of the Eocene/Oligocene boundary as 34 Ma. We anticipate that with concurrent work on a fundamental revision of the geomagnetic polarity sequence, a comprehensive and detailed new time scale for the Cenozoic will soon be developed

The Age of the 20 Meter Solo River Terrace, Java, Indonesia and the Survival of Homo erectus in Asia

Homo erectus was the first human lineage to disperse widely throughout the Old World, the only hominin in Asia through much of the Pleistocene, and was likely ancestral to H. sapiens. The demise of this taxon remains obscure because of uncertainties regarding the geological age of its youngest populations. In 1996, some of us co-published electron spin resonance (ESR) and uranium series (U-series) results indicating an age as young as 35–50 ka for the late H. erectus sites of Ngandong and Sambungmacan and the faunal site of Jigar (Indonesia). If correct, these ages favor an African origin for recent humans who would overlap with H. erectus in time and space. Here, we report 40Ar/39Ar incremental heating analyses and new ESR/U-series age estimates from the “20 m terrace" at Ngandong and Jigar. Both data sets are internally consistent and provide no evidence for reworking, yet they are inconsistent with one another. The 40Ar/39Ar analyses give an average age of 546±12 ka (sd±5 se) for both sites, the first reliable radiometric indications of a middle Pleistocene component for the terrace. Given the technical accuracy and consistency of the analyses, the argon ages represent either the actual age or the maximum age for the terrace and are significantly older than previous estimates. Most of the ESR/U-series results are older as well, but the oldest that meets all modeling criteria is 143 ka+20/−17. Most samples indicated leaching of uranium and likely represent either the actual or the minimum age of the terrace. Given known sources of error, the U-series results could be consistent with a middle Pleistocene age. However, the ESR and 40Ar/39Ar ages preclude one another. Regardless, the age of the sites and hominins is at least bracketed between these estimates and is older than currently accepted

Genomic, Pathway Network, and Immunologic Features Distinguishing Squamous Carcinomas

This integrated, multiplatform PanCancer Atlas study co-mapped and identified distinguishing molecular features of squamous cell carcinomas (SCCs) from five sites associated with smokin

Pan-Cancer Analysis of lncRNA Regulation Supports Their Targeting of Cancer Genes in Each Tumor Context

Long noncoding RNAs (lncRNAs) are commonly dys-regulated in tumors, but only a handful are known toplay pathophysiological roles in cancer. We inferredlncRNAs that dysregulate cancer pathways, onco-genes, and tumor suppressors (cancer genes) bymodeling their effects on the activity of transcriptionfactors, RNA-binding proteins, and microRNAs in5,185 TCGA tumors and 1,019 ENCODE assays.Our predictions included hundreds of candidateonco- and tumor-suppressor lncRNAs (cancerlncRNAs) whose somatic alterations account for thedysregulation of dozens of cancer genes and path-ways in each of 14 tumor contexts. To demonstrateproof of concept, we showed that perturbations tar-geting OIP5-AS1 (an inferred tumor suppressor) andTUG1 and WT1-AS (inferred onco-lncRNAs) dysre-gulated cancer genes and altered proliferation ofbreast and gynecologic cancer cells. Our analysis in-dicates that, although most lncRNAs are dysregu-lated in a tumor-specific manner, some, includingOIP5-AS1, TUG1, NEAT1, MEG3, and TSIX, synergis-tically dysregulate cancer pathways in multiple tumorcontexts