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791.
Potsdam sandstone from quarries and outcrops near 19th‐century glassworks sites in Redwood, NY, and Saranac, NY, Mallorytown, ON, and Como and Hudson, QC, commonly contains _97% silica, so in terms of its purity can compete with other historical producers of silica sand (e.g., Cheshire quartzite, MA; southern New Jersey sand). Exploratory analysis of trace element data using multidimensional scaling (MDS) shows that geographically distinct sources of Potsdam sandstone can be distinguished from one another and from competing sources of silica sand, particularly in terms of high field strength elements (e.g., Nb, Y, Ti, Zr), the rare earth elements, and radioactive elements (U, Th), and this geochemical signature is carried through to the glass it was used to manufacture. Other trace elements (e.g., Ba, Sr, Rb) are concentrated in various batch ingredients (e.g., limestone, alkali fluxes). The Hf/Nb, La/Ce, Nb/Th, and La/Zr ratios for each type of glass and nearby Potsdam sandstone sources cluster together in distinct fields on MDS plots. These data confirm the use of Potsdam sandstone in these important historical glassworks, and show that except for material sampled from neighboring communities (Mallorytown and Redwood), trace elements can be used to identify specific sources of silica historically used by the glassmaking industry. © 2008 Wiley Periodicals, Inc.  相似文献   
792.
This paper describes the results of the grain-size and mineralogical studies of the deposits of the tsunami of 1994 on Shikotan, Tanfil’ev, and Kunashir islands. The studies were carried out within the portions of the coast with different configurations, geomorphologic structures, lithodynamical environments, and character of the tsunami manifestation. The composition of the tsunami deposits is shown to be controlled mainly by erosion-accumulative processes during the tsunami events and is in many respects inherited from the matter sources. The tsunami deposits contain marine diatom species, whose richest assemblages were found within the areas where the material from the underwater coastal slope was redeposited. The data concerning the deposits of earlier historical tsunamis encountered in the same cross sections are discussed too. Their examination points to a similar development of the erosional-accumulative processes during tsunami events with the same intensity and an entrainment of the matter from the same sources.  相似文献   
793.
The Cerrado biome is the second largest in Brazil, but the evolution of the Cerrado during the late Quaternary is not yet fully known. This study identifies paleoenvironmental changes during the last 23 000 years, based on a tropical mountain peatland record, in the Serra do Espinhaço Meridional in central-eastern Brazil. A multi-proxy approach was used that involved palynological analysis, stable isotopes (δ13C, δ15N), geochemistry, radiocarbon dating and multivariate statistics derived from a peatland core from Rio Preto (Minas Gerais state). The study reveals a very humid and cold climate during the late Pleistocene, with an increase in temperature and decrease in humidity at the Pleistocene–Holocene transition. During this period there was strong instability in the landscape (episodes of erosion). At the beginning of the Holocene there was a reduction in humidity with greater landscape stability. The current sub-humid climatic conditions seem to have been established in the mid-/late Holocene, with periods of landscape instability. Our findings agree with other Cerrado records that contradict previously established hypotheses, such as the Amazonian Refuge and the Pleistocene Arc.  相似文献   
794.
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.  相似文献   
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