Wildfire preparedness,community cohesion and social–ecological systems

The consequences of wildfires are felt in susceptible communities around the globe on an annual basis. Climate change predictions in places like the south-east of Australia and western United States suggest that wildfires may become more frequent and more intense with global climate change. Compounding this issue is progressive urban development at the peri-urban fringe (wildland–urban interface), where continued infrastructure development and demographic changes are likely to expose more people and property to this potentially disastrous natural hazard. Preparing well in advance of the wildfire season is seen as a fundamental behaviour that can both reduce community wildfire vulnerability and increase hazard resilience – it is an important element of adaptive capacity that allows people to coexist with the hazardous environment in which they live. We use household interviews and surveys to build and test a substantive model that illustrates how social cohesion influences the decision to prepare for wildfire. We demonstrate that social cohesion, particularly community characteristics like ‘sense of community’ and ‘collective problem solving’, are community-based resources that support both the adoption of mechanical preparations, and the development of cognitive abilities and capacities that reduce vulnerability and enhance resilience to wildfire. We use the results of this work to highlight opportunities to transfer techniques and approaches from natural hazards research to climate change adaptation research to explore how the impacts attributed to the social components of social–ecological systems can be mitigated more effectively.     

Electron Density distribution and bonding in silicates

This paper summarizes the recent results of the investigation of bonding in silicates obtained by precision X-ray diffraction. The experimental electron density distribution is compared with theoretical electron density maps calculated for model silicate molecules. The characteristic features of the chemical bonds in ortho-, ring-, chain- and framework silicates are discussed.     

Mangrove ecology,aquatic primary productivity,and fish community dynamics in the Teacapán-Agua Brava Lagoon-Estuarine system (Mexican Pacific)

Aquatic primary productivity, mangrove ecology, and fish community dynamics were investigated in the Teacapán-Agua Brava lagoon-estuarine system, the most extensive mangrove ecosystem on the Pacific coast of Mexico with three species of mangroves distributed heterogeneously (Laguncularia racemosa, Rhizophora mangle, andAvicennia germinans). Tree density was 3,203 trees ha^?1 and basal area was 14.0 m² ha^?1. Litterfall was 1,417 g m^?2 yr^?1, characteristic of a productive riverine forest. The degradation constant forLaguncularia racemosa leaves varied from 1.71 to 4.7 yr^?1 and mean annual net aquatic productivity was 0.41 g C m^?3 d^?1. There were high concentrations of humic substances (up to 150 mg l^?1) early in the wet season. Seasonal variations of the above parameters seemed closely related to the ecology of fish populations. There were 75 fish species distributed in two principal assemblages associated with wet and dry seasons. Diversity and biomass analysis indicated 18 dominant species. Total biomass of the community in this coastal system was estimated at 10 g wet wt m^?2. The highest biomass occurred in the wet season. The most common fish species wereMugil curema, Achirus mazatlanus, Galeichthys caerulescens, Arius liropus, Diapterus peruvianus, Lile stolifera, Centropomus robalito, andEucinostomus sp., all of which have fishery importance. Primary productivity and fish community ecology are controlled by habitat characteristics, river discharge, and climatic seasonality.     

Slump debris flows in the Akovolwo Mountains area of Benue State,Nigeria

In September 1979, rain-induced complex landslides occurred in two separate localities along the slopes of the Akovolwo Mountains near Jato-Aka in the Kwande Local Government area of Benue State, Nigeria.The two movements developed on bedrock slopes covered by a veneer of colluvium and (or) residuum no more than 1.5 to 2m deep. Each started as a slump and graduated into a debris flow. The slump, extending downhill a short distance away from the head scarp, had been reconstituted into a debris flow as the initial movement (sliding movement) of the soil mass caused remoulding of the saturated moving mass into viscous debris-laden mud. The resulting mass moved partly along a pre-existing mountain stream channel and partly along a fresh channel it cleared in the savanna forest. At the break of slope, the mass of boulders was dumped and a trail of smaller fragments littered the channels towards the Katsina-Ala River.     

Experimental Petrology of Melilite Nephelinites

Experimental study of natural melilite nephelinite lavas ofintermediate K/Na ratio at low pressure (fo₂ reveals the presenceof a peritectic ‘point’ of distributary type (1090?C)for liquids saturated with leucite, nepheline, and spinel. Withdecreasing temperature on the olivine + melilite cotectic, botholivine and melilite react with such liquids to produce high-calciumpyroxene at the peritectic. Both the olivine + high-calciumpyroxene and melilite + high-calcium pyroxene cotectics arestable at temperatures below the peritectic. Olivines coexistingwith such liquids are much more magnesian than those in comparabletholeiitic liquids. The olivine-liquid Fe-Mg distribution coefficient is a monotonically increasing function of silica activity over the composition range spannedby melilite nephelinite, ugandite, alkali basalt, and tholeiitebasalt liquids. The analogous Fe-Mg distribution coefficientfor melilite and liquid is effectively constant , while that for high-calcium pyroxene and liquidis highly dependent on the chemistry of high-calcium pyroxene(cf., Sack & Carmichael, 1984). Pseudoternary liquidus projectionsof multiply saturated liquids coexisting with nepheline, leucite,and spinel (?olivine?high-calcium pyroxene?melilite) have beenprepared to facilitate graphical analysis of the evolution oflava compositions during hypabyssal cooling. Major element chemicalanalyses and petrographic features of lavas from Mt. Nyiragongo,East Africa and Oahu, Hawaii (e.g., Denaeyer et al., 1965; Wilkinson& Stolz, 1983) confirm the validity of these diagrams andthe systematics established from the experimental data. ^*Reprint requests to R.O. Sack     

The molecular composition of ambers

Bulk (elemental composition, IR, CP/MAS ¹³C NMR) and molecular (GC-MS) analyses have been performed on a series of ambers and resins derived from different locations (Dominican Republic, Philippines, Canada, Israel, New Zealand, Chile) having diverse botanical affinities (Araucariaceae, Hymenaea) and variable age (from Holocene to Early Cretaceous). No major differences have been observed from the elemental composition and the spectroscopic data; however, the molecular analyses of the solvent extractable fraction show that a specific mixture of components is present in each sample. These are mainly diterpenoid products that in general are also found abundantly in the higher plants from which the ambers and resins originate. Nevertheless, a direct relationship between major terpenoid constituents in fossil resins and precursor plant materials can only be established for the younger samples.Irrespective of the geographical or botanical origin of the ambers and resins, several common age-dependent molecular transformation trends can be recognized: (1) progressive loss of olefinic bonds (especially those located in exocyclic positions), (2) decrease of functionalized products, and (3) increasing proportion of aromatized components. However, even in the samples of older age (Cretaceous) the degree of aromatization is very low when compared with that of other higher-plant related materials such as fossilized woods or low rank coals. This indicates that maturation must involve essentially olefin polymerization processes instead of extensive aromatization.     

High temperature calorimetry of sulfide systems

The standard enthalpies of formation of FeS (troilite), FeS₂ (pyrite), Co_0.9342S, Co₃S₄ (linnaeite), Co₉S₈ (cobalt pentlandite), CoS₂ (cattierite), CuS (covellite), and Cu₂S (chalcocite) have been determined by high temperature direct reaction calorimetry at temperatures between 700 K and 1021 K. The following results are reported: $$\Delta {\rm H}_{f,FeS}^{tr} = - 102.59 \pm 0.20kJ mol^{ - 1} ,$$ $$\Delta {\rm H}_{f,FeS}^{py} = - 171.64 \pm 0.93kJ mol^{ - 1} ,$$ $$\Delta {\rm H}_{f,Co_{0.934} S} = - 99.42 \pm 1.52kJ mol^{ - 1} ,$$ $$\Delta {\rm H}_{f,Co_9 S_8 }^{ptl} = - 885.66 \pm 16.83kJ mol^{ - 1} ,$$ $$\Delta {\rm H}_{f,Co_3 S_4 }^{In} = - 347.47 \pm 7.27kJ mol^{ - 1} ,$$ $$\Delta {\rm H}_{f,CoS_2 }^{ct} = - 150.94 \pm 4.85kJ mol^{ - 1} ,$$ $$\Delta {\rm H}_{f,Cu_2 S}^{cc} = - 80.21 \pm 1.51kJ mol^{ - 1} ,$$ and $$\Delta {\rm H}_{f,CuS}^{cv} = - 53.14 \pm 2.28kJ mol^{ - 1} ,$$ The enthalpy of formation of CuFeS₂ (chalcopyrite) from (CuS+FeS) and from (Cu+FeS₂) was determined by solution calorimetry in a liquid Ni_0.60S_0.40 melt at 1100 K. The results of these measurements were combined with the standard enthalpies of formation of CuS, FeS, and FeS₂, to calculate the standard enthalpy of formation of CuFeS₂. We found \(\Delta {\rm H}_{f,CuFeS_2 }^{ccp} = - 194.93 \pm 4.84kJ mol^{ - 1}\) . Our results are compared with earlier data given in the literature; generally the agreement is good and our values agree with previous estimates within the uncertainties present in both.     

Modeling microclimate environments: A verification study

A numerical model is developed for simulating microclimate of plants and bare soil. The model evaluates heat, mass, momentum, and radiative fluxes in the soil-plant-atmosphere system. Its vertical domain may extend throughout the whole Planetary Boundary Layer (PBL). The model requires, either, temporal meteorological data of solar radiation, wind speed, air temperature and humidity measured over the field, or, when applied to the whole PBL, initial values of the latter three at its top. Vegetation parameters (leaf area index, photometric properties, root distribution and density) as well as soil texture, hydraulic and photometric properties are considered. The model was verified with meteorological data taken from two different climatological regions, above a bare soil and two cotton fields.For all case studies, observed and calculated values of air (except for within-canopy) and soil temperatures, wind speed, net radiation, and soil-, latent-, and sensible heat fluxes, agreed well with measurements.     

MODEL-BASED TRANSFORMATIONS OF COMMON MIDPOINT GATHERS1

A method for transforming Normal Moveout corrected CMP-gathers is proposed. The method is based upon the availability of a model of the CMP-gather. However, the transformation can be performed with any degree of accuracy in the model. Ideally the employed model should be a synthesis of all available a priori information about the particular data set. Mathematically the transformation is performed as follows. The CMP-gather is considered to be a matrix. This matrix is first decomposed into a set of submatrices of the same dimensions. Each submatrix consists of non-zero elements or samples with the same relative amount of noise. By reducing each of these submatrices to a vector (a trace) we get a new set of traces. This set then represents the transformed CMP-gather. The purpose of the transformation is to organize the CMP data in a form which makes it easier both to analyse the noise distribution and to take the necessary steps to improve the signal-to-noise ratio at the stacking stage. In principle the method incorporates the exploitation of multichannel recordings with the use of models. Several examples of transformed gathers and their applications to the improvement of real seismic data are shown.     

Fluid inclusion and stable isotope studies of Pb-Zn-fluorite-barite mineralization in the lower and middle Benue Trough,Nigeria

Lead-zinc-fluorite-barite veins in the lower and middle Benue Trough (Nigeria) are located within the Lower Cretaceous (Albian) carbonaceous shales, limestones, and arkosic sandstones of this intracontinental rift structure. The veins in the lower Benue Through consist of sphalerite + galena+marcasite ± chalcopyrite ± barite in a gangue of siderite and quartz hosted by carbonaceous shales, whereas in the middle Benue Trough, fluorite, barite, quartz, and similar sulfide minerals are hosted by limestone and sandstone. Fluid inclusion temperatures in vein minerals range from 95°C to 200°C (without pressure corrections) and salinities range from 14 to 24 equiv. wt% NaCl. Oxygen isotope compositions of limestone wall rocks (middle Benue) have been lowered from premineralization ¹⁸O values of about 25 per mil to approximately 16 per mil. Fluid in equilibrium with vein calcite has a calculated ¹⁸O of +2.6 per mil at 130°C. The ⁸⁷Sr/⁸⁶Sr ratio of this calcite (0.71497) suggests that strontium and calcium had a considerably more radiogenic source than the Cretaceous limestone or evaporite did (⁸⁷Sr/⁸⁶Sr=0.7073–0.7078). Observed strontium data, lead isotope compositions of galena, and REE patterns in fluorite suggest that the Lower Paleozoic basement rocks in the trough or their weathered equivalents are likely sources for the Benue Trough ore components. Sulfur isotope data suggest that the sulfur was probably contributed from the Cretaceous evaporites in the trough.Our data favor a basinal brine source for the ore-forming fluid. Fluid criculation probably resulted from high geothermal gradients accompanying continental rifting. Brine interaction with the clastic, carbonate, and evaporite rocks led to metal and sulfur leaching and later deposition in fractures accompanying the Cenomanian deformation and uplift in the Benue Trough.