Particle transport mechanics and induced seismic noise in steep flume experiments with accelerometer-embedded tracers

Recent advances in fluvial seismology have provided solid observational and theoretical evidence that near-river seismic ground motion may be used to monitor and quantify coarse sediment transport. However, inversions of sediment transport rates from seismic observations have not been fully tested against independent measurements, and thus have unknown but potentially large uncertainties. In the present study, we provide the first robust test of existing theory by conducting dedicated sediment transport experiments in a flume laboratory under fully turbulent and rough flow conditions. We monitor grain-scale physics with the use of ‘smart rocks’ that consist of accelerometers embedded into manufactured rocks, and we quantitatively link bedload mechanics and seismic observations under various prescribed flow and sediment transport conditions. From our grain-scale observations, we find that bedload grain hop times are widely distributed, with impacts being on average much more frequent than predicted by existing saltation models. Impact velocities are observed to be a linear function of average downstream cobble velocities, and both velocities show a bed-slope dependency that is not represented in existing saltation models. Incorporating these effects in an improved bedload-induced seismic noise model allows sediment flux to be inverted from seismic noise within a factor of two uncertainty. This result holds over nearly two orders of magnitude of prescribed sediment fluxes with different sediment sizes and channel-bed slopes, and particle–particle collisions observed at the highest investigated rates are found to have negligible effect on the generated seismic power. These results support the applicability of the seismic-inversion framework to mountain rivers, although further experiments remain to be conducted at sediment transport near transport capacity. © 2018 John Wiley & Sons, Ltd.     

Palaeogeographic Changes at Lake Chokrak on the Kerch Peninsula,Ukraine, during the Mid‐ and Late‐Holocene

This project has reconstructed the palaeogeographic and environmental evolution of Lake Chokrak on the Kerch Peninsula, Ukraine, during the mid‐ and late‐Holocene. This record has been evaluated in association with a regional archaeological data set to explore human–environment interactions over this period. The results show major changes in the palaeogeographic setting of Lake Chokrak since the 3rd millennium B.C., when the postglacial marine transgression had started to fill the study area. Microfaunal analyses reveal the long persistence of an open marine embayment that only became separated from the Sea of Azov when a sand barrier developed during the late 2nd millennium B.C. When colonizing the Black Sea region after the 8th century B.C., the Greek settlers erected a fortification with a small settlement on a promontory that was by then a peninsula‐like headland extending into the lake. The colonists abandoned their settlement at the end of the 1st millennium B.C. when the depth of the surrounding lake decreased from 1.5 m to less than 1 m. Today, Lake Chokrak dries up completely during summer. A detailed relative sea level (RSL) curve for the northern coast of Kerch has been established. Sea level reached its highest position at the present day. Since the 3rd millennium B.C., sea level continuously rose, without any of the previously postulated regression/transgression cycles. The RSL curve indicates differential subsidence rates within short distances in relatively stable areas, exceeding 40 cm per 1000 years. © 2012 Wiley Periodicals, Inc.     

Geochemical and mineralogical distinctions between Bonnin and Morris (Philadelphia, 1770–1772) porcelain and some contemporary British phosphatic wares

The major element compositions of 15 ceramic sherds from the Bonnin and Morris factory site were determined by electron microprobe. Thirteen samples are phosphatic; the others consist of (a) “soapstone” (magnesian/plombian) and (b) true porcelain, and are interpreted as exotic artifacts, as is one compositionally distinct (relatively SiO₂‐poor, P₂O₅+CaO‐rich) phosphatic sample. Although long considered to be virtually indistinguishable from Bow porcelain (London: ca. 1747–1776), the phosphatic Philadelphia wares have a relatively low mean CaO/P₂O₅ ratio (3.3 versus 3.8; molecular proportions) and high alumina content (6.6 versus 5.4 wt % Al₂O₃). Furthermore, unlike Bow, the Bonnin and Morris samples contain calcic plagioclase (bytownite), and in some instances, an orthoclase‐rich ternary feldspar. The preservation of calcic plagioclase indicates that Philadelphia porcelain was fired at (rather than above) the thermal minimum in the An‐SiO₂‐C₃P system, although the presence of Na (and other fluxes) in these wares precludes the exact determination of the maximum firing temperature from this phase diagram. These wares are also distinctive insofar as the phosphate and melt phases can contain small amounts of lead; they have bulk lead contents of approximately 0.1–1.2 wt % PbO. This component has not been detected in the body of Bow or other contemporary British phosphatic porcelains. Their principal similarity lies in the fact that both wares contain sulfate. In addition, the glazes on Bonnin and Morris porcelain (e.g., PbO ∼ 35–50 wt %; SnO₂ ∼ 1–2%) compositionally resemble those used at Bow. If feldspar is formed at all, then Al‐poor phosphatic porcelain (or those with low CaO/P₂O₅ ratios) will have comparatively low modal calcic plagioclase contents, thereby allowing the rapid depletion of this mineral via resorption by the melt phase during vitrification. Such appears to have been the case for analyzed Bow porcelain, which is therefore interpreted to have been overfired (sensu lato) relative to its Philadelphia counterpart. Conceivably, calcic plagioclase could be preserved in low‐Al wares that were fired only briefly at vitrification temperatures. Given the role of firing history in governing the mineralogy of porcelain, compositional criteria are more reliable for distinguishing these wares. © 2001 John Wiley & Sons, Inc.