Late Holocene relative sea level rise and the Neoglacial history of the Greenland ice sheet

In West Greenland, early and mid Holocene relative sea level (RSL) fall was replaced by late Holocene RSL rise during the Neoglacial, after 4–3 cal. ka BP (thousand calibrated years before present). Here we present the results of an isolation basin RSL study completed near to the coastal town of Sisimiut, in central West Greenland. RSL fell from 14 m above sea level at 5.7 cal. ka BP to reach a lowstand of ?4.0 m at 2.3–1.2 cal. ka BP, before rising by an equivalent amount to present. Differences in the timing and magnitude of the RSL lowstand between this and other sites in West and South Greenland record the varied interplay of local and non‐Greenland RSL processes, notably the reloading of the Earth's crust caused by a Neoglacial expansion of the Greenland Ice Sheet (GIS) and the subsidence associated with the collapse of the Laurentide Ice Sheet forebulge. This means that the timing of the sea level lowstand cannot be used to infer directly when the GIS advanced during the Neoglacial. The rise in Late Holocene RSL is contrary to recently reported bedrock uplift in the Sisimiut area, based on repeat GPS surveys. This indicates that a belt of peripheral subsidence around the current ice sheet margin was more extensive in the late Holocene, and that there has been a switch from subsidence to uplift at some point in the last thousand years or so. Copyright © 2008 John Wiley & Sons, Ltd.     

The effect of chlorine and chlorine dioxide on pathogenic free‐living amoebae (PFLA) in simulated natural conditions: The presence of bacteria and organic matter

Bacteria and bovine faecal matter were introduced into cultures of pathogenic free‐living amoebae, with chlorine or chlorine dioxide. The bacteria and faeces were to simulate natural conditions for a more exacting test of disinfectant demand when compared to axenic conditions. Both chlorine and chlorine dioxide were effective disinfectants under all conditions tested. Axenically and monoxenically cultured amoebae were used, the latter exerted a greater disinfectant demand.     

Chemistry of micas from kimberlites and xenoliths—II. Primary- and secondary-textured micas from peridotite xenoliths

Micas from coarse granular Iherzolites in S. African kimberlites may be separated into two groups; those showing primary textural relationships with coexisting silicates and those with secondary, alteration relationships with other silicates. Primary-textured micas form a tight cluster with a mean composition from 10 coarse garnet lherzolites of: SiO₂ 41.0, TiO₂ 0.18, Al₂O₃ 13.5, Cr₂O₃ 0.82, total Fe as FeO 2.60, MnO 0.02, MgO 26.0, NiO 0.22, CaO 0.01, BaO 0.29, Na₂O 0.31, K₂O 10.0, Rb₂O 0.028, Cl 0.08, F 0.43 wt%. Primary-textured micas in aggregates with clinopyroxene have higher TiO₂ and four specimens which look similar to the primary group but have textural ambiguities have still higher TiO₂Micas with secondary textures have wide ranges of composition which may be correlated with details of the textural parageneses. Micas from kelyphitic rims around garnets tend to be Cr-rich while those from veinlets are Cr-poor. Both groups tend to have higher FeO and TiO₂ than the primary group. Micas produced by alteration of, or filling veinlets through, orthopyroxene have a wide compositional range which overlaps that of the primary-textured micas, especially for harzburgite specimens.The primary-textured micas show a positive correlation with coexisting pyroxenes for MgO/(MgO + FeO) and TiO₂, but not for Cr₂O₃. Secondary-textured micas do not show correlations with coexisting pyroxenes for any elements.The ‘primary-metasomatic’ micas described by Harte and Gurney (1975) and metasomatic and other micas described by Boettcher et al. (1979) and Boettcher and O'neil (1979) are richer in FeO and TiO₂ than the present primary-textured micas, and are attributed to crystallization from fractionated fluids.     

Fertile and barren AlCr-spinel harzburgites from the upper mantle: Ion and electron probe analyses of trace elements in olivine and orthopyroxene: Relation to lherzolites

Ion and electron microprobe analyses of twenty-one CrAl-spinel harzburgite xenoliths from southern African kimberlites show two chemical groups. Orthopyroxenes from “fertile” harzburgites have higher CaO (mean of 11, 0.95 wt.%), Al₂O₃ (3.05 wt.%), Cr₂O₃ (0.85 wt.%) and Li (0.8 ppmw) than those from “barren” harzburgites (mean of 10, CaO 0.24 wt.%, Al₂O₃ 1.10 wt.%, Cr₂O₃ 0.35 wt.%, Li 0.3 ppmw). Olivines from all harzburgites have similar chemistry except that mean values of Li and Na are higher for barren than fertile harzburgites (Li 0.9 vs. 0.4 ppmw; Na₂O 16 vs. 7 ppmw). Orthopyroxenes from fertile harzburgites are chemically distinct from those in garne lherzolites from southern Africa and spinel lherzolites from southwest U.S.A., but orthopyroxenes from barren harzburgites are indistinguishable from those in many coarse garnet lherzolites.Chromium, Ca, Ni, Na and Li in coexisting olivines and orthopyroxenes from the above rock types show complex patterns, which for Ca, Cr and Ni can be related to pressure and temperature. Temperatures from an empirically calibrated thermometer based on Ni-Mg exchange between olivine and orthopyroxene, measured modes of harzburgites (fertile, mean of 10: ol 68, opx 31, spinel-silicate intergrowth <0.5; barren, mean of 8: ol 76, opx 23, spinel and spinel-silicate intergrowth 1), and high-pressure experimental studies suggest (a) that harzburgites are residues of partial melting, (b) that barren harzburgites were melted to a greater extent at a higher temperature (though probably at a similar depth) than fertile harzburgites, and (c) that incomplete reequilibration during retrograde metamorphism has led to development of complex inter- and intragranular textures, probably in the range ～700–900°C.     

PCBs in the firth of clyde

Attention to detail is essential for the reduction of pollution. By detective work, a river purification board has been able to track down an important single source of PCB contamination of its sewage sludge and institute remedial action.     

B-polarization induction in two thin half-sheets coupled to the mantle by a conducting crust—II. Solution by the mode-matching method, the fields above the conductors, and example results

The mode-matching method is used to obtain an exact analytical solution to the problem of B -polarization induction in two adjacent thin half-sheets, lying on a conducting layer that is terminated by a perfect conductor at finite depth. These components of the model represent, respectively, the Earth's conducting surface layers, crust, and mantle. In dimensionless variables, the model has three independent parameters, these being the two thin-sheet conductances and the layer thickness. The mode-matching solution obtained in this paper is shown to be identical lo that derived via the Wiener-Hopf method in a companion paper (Dawson 1996), and so provides additional verification of that solution. As was shown in the companion paper, the solution for the present model contains, as special limiting cases, those for three models considered earlier by various authors. The second part of the present paper addresses the solutions for the electric fields in the non-conducting half-space above the conductors, which represents the atmosphere. In the final part, sample numerical calculations are presented to illustrate the solution.     

Confronting the challenge of integrated assessment of climate adaptation: a conceptual framework

Key limitations of integrated assessment models (IAMs) are their highly stylized and aggregated representation of climate damages and associated economic responses, as well as the omission of specific investments related to climate change adaptation. This paper proposes a framework for modeling climate impacts and adaptation that clarifies the relevant research issues and provides a template for making improvements. We identify five desirable characteristics of an ideal integrated assessment modeling platform, which we elaborate into a conceptual model that distinguishes three different classes of adaptation-related activities. Based on these elements we specify an impacts- and adaptation-centric IAM, whose optimality conditions are used to highlight the types of functional relationships necessary for realistic representations of adaptation-related decisions, the specific mechanisms by which these responses can be incorporated into IAMs, and the ways in which the inclusion of adaptation is likely to affect the simulations’ results.