Gelification of victorian tertiary soft brown coal wood. II. Changes in chemical structure associated with variation in the degree of gelification

The gross chemical structures of xylites and gelified soft brown coal woods, Latrobe Valley, Victoria, Australia, as determined by solid state nuclear magnetic resonance spectroscopy, are compared with those of present-day wood-derived materials prepared from an angiosperm, Eucalyptus regnans, and a gymnosperm (conifer), Pinus radiata. Also examined are the changes in the gross chemical structures of soft brown coal woods with increase in their degree of gelification and the relationship between these changes and variations in their chemical composition and microscopic appearance.The Victorian xylites exhibit greater affinities with the present-day gymnosperm than the present-day angiosperm. The progressive removal of cellulose with increasing degree of gelification can be equated with an increase in huminite reflectance, elimination of humotelinite autofluorescence and changes in the relative proportions of the humotelinite submacerals. The lignin structure of xylite is also modified during the gelification process, including the progressive loss of methoxyl groups and evidence of minor oxidation.     

Structure,composition and bulk properties of upland stream gravels

Upland gravel-bedded streams in the U.K. have received only scant attention from both hydrologists and sedimentologists, but are worthy of further investigation. The sedimentology of three small streams in Teesdale in the Pennines has been examined in detail. Grain-size characteristics, bedforms, structure, composition and packing characteristics of these deposits are described, and compared where appropriate with published information. It is argued that a fuller appreciation of gravel bed composition and morphology should eventually contribute to an improved understanding of sediment transport and deposition mechanisms, and, hence, to improved accuracy in sediment transport and deposition estimates.     

Regional variability in relationships between climate and dengue/DHF in Indonesia

Since 1970, the worldwide distribution, frequency and intensity of epidemics of dengue and dengue haemorrhagic fever (DHF) have increased dramatically. In Indonesia, as elsewhere, the geographic distribution and behaviour of the two main vectors – Aedes aegypti and Aedes albopictus – and the consequent transmission dynamics of the disease are strongly influenced by climate. Monthly incidence data were examined in relation to monthly data for temperature, rainfall, rainfall anomalies, humidity and the Southern Oscillation Index for 1992–2001. Focusing on eight provinces, significant Pearson correlations were observed between dengue/DHF incidence and at least one climate variable ( r  = ±0.2 to ±0.43; P  < 0.05). Multiple regression analyses showed that 12.9–24.5 per cent of variance in incidence was explained by two or three climate variables in each province ( P  < 0.1–0.01). Rainfall appears to be the principal climatic agent affecting the geographic distribution and temporal pattern of incidence while temperature appears to play a critical role in outbreak intensity. Wide regional and temporal variations in the strength and nature of the observed associations led to the identification of three groups of provinces where increases in dengue/DHF incidence were variously associated with increased rainfall, decreased rainfall and/or high susceptibility to climate variability. Although climatic factors play an important role in explaining the timing and intensity of dengue/DHF outbreaks, a wide range of other factors specific to local environments also appear to be involved – information that may assist in the prediction and mitigation of regional dengue/DHF outbreaks.     

Effectiveness of simple approaches in mitigating residual deformations in buildings

Developments in performance‐based seismic design and assessment approaches have emphasized the importance of considering residual deformations. Recent investigations have also led to a proposed direct displacement‐based design (DDBD) approach which includes an explicit consideration of the expected residual deformations as an integral part of the design process. Having estimated the expected residual deformations in a structure, engineers are faced with the problem of reducing them to meet the targeted performance levels under pre‐defined seismic hazard levels. Previous studies have identified the post‐yield stiffness as a primary factor influencing the magnitude of residual deformations in single degree of freedom and multiple degree of freedom structures. In this paper, a series of simple approaches to increase the post‐yield stiffness of traditional framed and braced systems for the purpose of reducing residual deformations are investigated. These methods do not utilize recentring post‐tensioned technology. This contribution addresses the feasibility of altering the lateral post‐yield stiffness of structural systems by: (i) using different reinforcement materials with beneficial features in their stress–strain behaviour; (ii) re‐designing the section geometry and properties of primary seismic‐resisting elements; and (iii) introducing a secondary elastic frame to act in parallel with the primary system. The efficiency of each of these techniques is investigated through monotonic and cyclic moment‐curvature and non‐linear time‐history analyses. Of these approaches the design and introduction of an elastic secondary system was found to be most effective and consistent in reducing residual deformations. A simplified design approach for achieving the desired increase of a system's post‐yield stiffness is also presented. Copyright © 2007 John Wiley & Sons, Ltd.     

Adapting to climate change: Public water supply in England and Wales

This paper describes an assessment of the ways in which water supply companies in England and Wales are adapting to climate change, evaluated in the context of a model of the adaptation process. The four components of the model are (i) awareness of and concern about the potential impacts of climate change, (ii) adaptation strategy, (iii) the concept of an adaptation space from which options are selected, and (iv) the notion that three groups of factors influence awareness, strategy and option selection: susceptibility to change, internal characteristics of the organisation, and regulatory and market context.Public water supply in England and Wales is provided by private sector companies, subject to environmental and economic regulation. Hydrological simulations suggest that climate change has the potential to reduce the reliability of supply sources over the next few decades. The industry in December 2004 completed a review of investment requirements over the next five years.Awareness of climate change is high in the water industry, but by developing assessment procedures and incorporating them into the investment review the regulators forced companies to consider explicitly the potential impacts of climate change in a consistent and rigorous manner. These analyses combined climate change with other pressures on water resources, and in practice companies did not attribute specific investment decisions or proposals to climate change or indeed any other individual drivers. The broad strategy adopted by all water supply companies – to maintain standards of service – is determined by regulatory controls and market considerations, but the degree of concern about the impacts of climate change and precise adaptation options necessary to address supply-demand imbalances varied between water supply companies, reflecting local geographic conditions. The water supply companies and regulators have different perspectives on the relative merits of supply-side and demand-side measures, reflecting different organisational priorities.The 2004 investment review determined that no specific actions were necessary to deal with future climate change, but that measures set in place – in terms of methodologies and investment in investigations into specific resource developments – provided a sound foundation for more specific actions in the next investment review in five years time. The paper concludes by summarising the factors assisting and constraining adaptation over the next few decades.     

Gas adsorption on crushed quartz and basalt

The new surfaces generated by crushing rocks and minerals adsorb gases. Different gases are adsorbed to different extents so that both the total amount and composition of the released gases are changed. This affects the interpretation of the composition of the gases obtained by vacuum crushing lunar basalts, meteorites and minerals with fluid inclusions.     

High-Ca,low-alkali carbonatite volcanism at Fort Portal,Uganda

A Quaternary volcanic field at Fort Portal, SW Uganda, contains approximately 50 vents that erupted only carbonatite. The vents are marked by monogenetic tuff cones defining two ENE-trending belts. Lava from a fissure at the west end of the northern belt formed a flow 0.3 km² in area and 1–5 m thick. The lava is vesicular throughout with a scoriaceous top, and probably formed by agglutination of spatter from lava fountains. Phenocrysts are olivine, clinopyroxene, phlogopite, and titanomagnetite enclosing blebs of pyrrhotite. Rims of monticellite, gehlenite, and reinhardbraunsite surround olivine, clinopyroxene and phlogopite, and magnetite is rimmed by spinel. The reaction relations suggest that these phenocryst phases are actually xenocrysts, perhaps from a source similar to that which supplied phlogopite clinopyroxenite xenoliths in the Katwe-Kikorongo volcanic field 75 km SW of Fort Portal. The groundmass of fresh carbonatite lava consists of tabular calcite, spurrite, periclase, hydroxylapatite, perovskite, spinel, pyrrhotite, and barite. The lava was readily altered; where meteoric water had access, spurrite and periclase are lacking, and some calcite is recrystallized. Vesicles in lava and rare dike rocks are partly filled with calcite, followed by jennite and thaumasite. Pyroclastic deposits cover 142 km² and are far more voluminous than lava. Carbonatite ejecta were identical to lava in primary mineralogy, but are much more contaminated by crustal rock fragments and xenocrysts. At Fort Portal, eruption of a CaO-MgO-CO₂-SiO₂-P₂O₅-SO₂-H₂O-F liquid was unaccompanied by that of a more silica-rich or alkali-rich liquid. Alkali-rich carbonatite lavas and pyroclastic deposits have been documented elsewhere in East Africa, and calcite-rich volcanic carbonatites have been attributed to replacement of magmatic alkali carbonates by calcite. However, the alkali-poor volcanic carbonatites at Fort Portal were not formed by leaching of alkalis in meteoric water; tabular calcite is not pseudomorphous after alkali carbonates such as nyerereite. The Fort Portal magma was low in alkalis at the time of eruption.     

Anaerobic methane oxidation and a deep H2S sink generate isotopically heavy sulfides in Black Sea sediments

The main terminal processes of organic matter mineralization in anoxic Black Sea sediments underlying the sulfidic water column are sulfate reduction in the upper 2-4 m and methanogenesis below the sulfate zone. The modern marine deposits comprise a ca. 1-m-deep layer of coccolith ooze and underlying sapropel, below which sea water ions penetrate deep down into the limnic Pleistocene deposits from >9000 years BP. Sulfate reduction rates have a subsurface maximum at the SO₄²⁻-CH₄ transition where H₂S reaches maximum concentration. Because of an excess of reactive iron in the deep limnic deposits, most of the methane-derived H₂S is drawn downward to a sulfidization front where it reacts with Fe(III) and with Fe²⁺ diffusing up from below. The H₂S-Fe²⁺ transition is marked by a black band of amorphous iron sulfide above which distinct horizons of greigite and pyrite formation occur. The pore water gradients respond dynamically to environmental changes in the Black Sea with relatively short time constants of ca. 500 yr for SO₄²⁻ and 10 yr for H₂S, whereas the FeS in the black band has taken ca. 3000 yr to accumulate. The dual diffusion interfaces of SO₄²⁻-CH₄ and H₂S-Fe²⁺ cause the trapping of isotopically heavy iron sulfide with δ³⁴S = +15 to +33‰ at the sulfidization front. A diffusion model for sulfur isotopes shows that the SO₄²⁻ diffusing downward into the SO₄²⁻-CH₄ transition has an isotopic composition of +19‰, close to the +23‰ of H₂S diffusing upward. These isotopic compositions are, however, very different from the porewater SO₄²⁻ (+43‰) and H₂S (−15‰) at the same depth. The model explains how methane-driven sulfate reduction combined with a deep H₂S sink leads to isotopically heavy pyrite in a sediment open to diffusion. These results have general implications for the marine sulfur cycle and for the interpretation of sulfur isotopic data in modern sediments and in sedimentary rocks throughout earth’s history.